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    "not_specified": 985498,
    "Brown-Vialetto-van_Laere_syndrome_1|Progressive_bulbar_palsy_of_childhood": 2,
    "not_provided": 863116,
    "not_specified|not_provided": 19283,
    "SAMD11-related_disorder": 6,
    "SAMD11-related_disorder|not_provided": 21,
    "not_provided|not_specified": 17394,
    "not_provided|SAMD11-related_disorder": 17,
    "SAMD11-related_disorder|not_specified|not_provided": 2,
    "not_provided|Retinal_dystrophy": 836,
    "Retinal_dystrophy|not_provided|not_specified": 18,
    "Retinal_dystrophy": 3278,
    "Retinal_dystrophy|not_specified|not_provided": 38,
    "Optic_atrophy|not_provided|not_specified": 1,
    "not_specified|not_provided|Retinal_dystrophy": 24,
    "Retinal_dystrophy|not_specified": 11,
    "Retinitis_pigmentosa|not_provided": 403,
    "not_provided|Neutrophil_inclusion_bodies": 1,
    "Retinal_dystrophy|not_provided": 1090,
    "Esophageal_atresia/tracheoesophageal_fistula": 19,
    "KLHL17-related_condition": 1,
    "Autism_spectrum_disorder": 397,
    "Neutrophil_inclusion_bodies|Renal_tubular_epithelial_cell_apoptosis|not_specified": 1,
    "Congenital_myasthenic_syndrome_8": 1602,
    "not_specified|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency": 8,
    "not_specified|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|not_provided": 3,
    "ISG15-related_disorder": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency": 103,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|not_specified": 6,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency": 5,
    "not_specified|not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency": 3,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|not_provided": 4,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|ISG15-related_disorder": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|not_provided|not_specified": 1,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|not_specified": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency|not_specified|not_provided": 1,
    "ISG15-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_ISG15_deficiency": 1,
    "Inborn_genetic_diseases": 185055,
    "Congenital_myasthenic_syndrome_8|not_provided|AGRN-related_disorder": 6,
    "not_specified|Congenital_myasthenic_syndrome_8|not_provided": 16,
    "Congenital_myasthenic_syndrome_8|not_provided|Inborn_genetic_diseases": 6,
    "Congenital_myasthenic_syndrome_8|Inborn_genetic_diseases": 82,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_8|AGRN-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8": 134,
    "AGRN-related_disorder": 9,
    "AGRN-related_disorder|Congenital_myasthenic_syndrome_8": 17,
    "Congenital_myasthenic_syndrome_8|not_provided": 50,
    "not_provided|Congenital_myasthenic_syndrome_8": 48,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8|not_provided": 8,
    "not_specified|Congenital_myasthenic_syndrome_8": 16,
    "Congenital_myasthenic_syndrome_8|Congenital_myasthenic_syndrome": 7,
    "Congenital_myasthenic_syndrome": 107,
    "AGRN-related_disorder|Congenital_myasthenic_syndrome_8|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_8": 6,
    "Congenital_myasthenic_syndrome_8|not_specified": 14,
    "not_provided|Congenital_myasthenic_syndrome_8|not_specified": 11,
    "Congenital_myasthenic_syndrome_8|not_provided|Inborn_genetic_diseases|AGRN-related_disorder": 1,
    "Inborn_genetic_diseases|AGRN-related_disorder|not_provided|Congenital_myasthenic_syndrome_8": 1,
    "Congenital_myasthenic_syndrome_8|not_provided|not_specified|AGRN-related_disorder": 1,
    "AGRN-related_disorder|Congenital_myasthenic_syndrome_8|not_provided": 6,
    "Presynaptic_congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_8": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_8": 6,
    "Inborn_genetic_diseases|not_provided": 21881,
    "Abnormality_of_the_musculature": 61,
    "See_cases|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_8": 11,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8|not_specified": 1,
    "Congenital_myasthenic_syndrome_8|AGRN-related_disorder": 8,
    "Congenital_myasthenic_syndrome_8|not_specified|not_provided": 13,
    "not_provided|Inborn_genetic_diseases": 20550,
    "not_specified|Congenital_myasthenic_syndrome_8|AGRN-related_disorder": 1,
    "Congenital_myasthenic_syndrome_8|not_provided|not_specified": 7,
    "AGRN-related_disorder|Congenital_myasthenic_syndrome_8|not_specified|not_provided": 1,
    "not_provided|AGRN-related_disorder|Congenital_myasthenic_syndrome_8": 3,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8": 10,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome_8|AGRN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "AGRN-related_disorder|not_provided|Congenital_myasthenic_syndrome_8": 2,
    "AGRN-related_disorder|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_8|not_specified|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_8|Inborn_genetic_diseases": 2,
    "AGRN-related_disorder|Congenital_myasthenic_syndrome_8|not_specified": 2,
    "Inborn_genetic_diseases|AGRN-related_disorder|Congenital_myasthenic_syndrome_8": 2,
    "Congenital_myasthenic_syndrome_8|AGRN-related_disorder|not_provided": 2,
    "AGRN-related_disorder|not_specified|Congenital_myasthenic_syndrome_8": 1,
    "Congenital_myasthenic_syndrome_8|Inborn_genetic_diseases|not_provided": 2,
    "See_cases|Congenital_myasthenic_syndrome_8": 2,
    "Inborn_genetic_diseases|See_cases": 38,
    "not_specified|AGRN-related_disorder|Congenital_myasthenic_syndrome_8|not_provided": 1,
    "Congenital_myasthenic_syndrome_8|Neurodevelopmental_disorder": 1,
    "not_provided|Congenital_myasthenic_syndrome_8|AGRN-related_disorder": 1,
    "Neurodevelopmental_disorder": 657,
    "Congenital_myasthenic_syndrome_8|not_specified|not_provided|AGRN-related_disorder|Inborn_genetic_diseases": 1,
    "Combined_immunodeficiency_due_to_OX40_deficiency": 250,
    "Combined_immunodeficiency_due_to_OX40_deficiency|not_provided": 6,
    "not_specified|Combined_immunodeficiency_due_to_OX40_deficiency": 10,
    "not_provided|Combined_immunodeficiency_due_to_OX40_deficiency": 9,
    "Combined_immunodeficiency_due_to_OX40_deficiency|TNFRSF4-related_disorder": 1,
    "Combined_immunodeficiency_due_to_OX40_deficiency|not_specified": 28,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_OX40_deficiency": 1,
    "TNFRSF4-related_disorder|not_provided|Combined_immunodeficiency_due_to_OX40_deficiency": 1,
    "TNFRSF4-related_disorder": 1,
    "TNFRSF4-related_disorder|Combined_immunodeficiency_due_to_OX40_deficiency": 1,
    "not_provided|Combined_immunodeficiency_due_to_OX40_deficiency|not_specified": 1,
    "not_provided|TNFRSF4-related_disorder|Combined_immunodeficiency_due_to_OX40_deficiency": 1,
    "Combined_immunodeficiency_due_to_OX40_deficiency|not_specified|not_provided": 1,
    "Combined_immunodeficiency_due_to_OX40_deficiency|TNFRSF4-related_disorder|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 45,
    "Al-Gazali_syndrome|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures": 2,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|not_provided|B3GALT6-related_disorder|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 119,
    "not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 15,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided": 6,
    "Al-Gazali_syndrome|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|Inborn_genetic_diseases|not_provided|not_specified|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_specified": 1,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|not_provided": 14,
    "B3GALT6-related_disorder": 5,
    "B3GALT6-related_disorder|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 2,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Inborn_genetic_diseases": 7,
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    "not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Inborn_genetic_diseases": 4,
    "Al-Gazali_syndrome|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|not_specified": 3,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures": 6,
    "not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 3,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 2,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 5,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_fractures": 2,
    "B3GALT6-related_disorder|not_specified|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 1,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|not_specified|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 3,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 2,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Inborn_genetic_diseases|not_provided": 2,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "B3GALT6-related_disorder|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided": 2,
    "Al-Gazali_syndrome": 2,
    "not_provided|B3GALT6-related_disorder|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "B3GALT6-related_disorder|not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures": 1,
    "not_specified|not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Inborn_genetic_diseases": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|B3GALT6-related_disorder": 2,
    "not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_fractures|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided|Al-Gazali_syndrome|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures": 1,
    "not_provided|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|not_specified": 1,
    "not_specified|not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|B3GALT6-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_fractures|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|Inborn_genetic_diseases": 690,
    "Spondyloepiphyseal_dysplasia": 3,
    "Al-Gazali_syndrome|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|B3GALT6-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2": 1,
    "not_specified|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Al-Gazali_syndrome|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|not_provided": 1,
    "Al-Gazali_syndrome|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_1|_with_or_without_fractures|not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity": 1,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_2|B3GALT6-related_disorder|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder_with_motor_and_language_delay|_ocular_defects|_and_brain_abnormalities": 9,
    "Neurodevelopmental_disorder_with_motor_and_language_delay|_ocular_defects|_and_brain_abnormalities|not_specified": 4,
    "DVL1-related_disorder": 9,
    "Autosomal_dominant_Robinow_syndrome_1": 49,
    "Autosomal_dominant_Robinow_syndrome_2|not_provided|DVL1-related_disorder": 1,
    "DVL1-related_disorder|not_provided": 17,
    "not_provided|DVL1-related_disorder": 11,
    "Autosomal_dominant_Robinow_syndrome_2|not_provided": 9,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Robinow_syndrome_2": 1,
    "See_cases": 1216,
    "not_provided|Autosomal_dominant_Robinow_syndrome_2": 9,
    "not_provided|Intellectual_disability": 107,
    "Autosomal_dominant_Robinow_syndrome_2": 24,
    "Autosomal_dominant_Robinow_syndrome_1|Autosomal_dominant_Robinow_syndrome_2": 1,
    "not_provided|Autosomal_dominant_Robinow_syndrome_1|Autosomal_dominant_Robinow_syndrome_2": 1,
    "Autosomal_dominant_Robinow_syndrome_1|Autosomal_dominant_Robinow_syndrome_2|not_provided|DVL1-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_Robinow_syndrome_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|DVL1-related_disorder": 1,
    "not_provided|Autosomal_dominant_Robinow_syndrome_2|Inborn_genetic_diseases": 1,
    "not_specified|DVL1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Robinow_syndrome_1": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Robinow_syndrome_2|Autosomal_dominant_Robinow_syndrome_1": 1,
    "not_provided|not_specified|Inborn_genetic_diseases": 269,
    "Autosomal_dominant_Robinow_syndrome_2|Inborn_genetic_diseases": 1,
    "Ciliary_dyskinesia|_primary|_40": 44,
    "MXRA8-related_disorder": 9,
    "Abnormal_brain_morphology": 36,
    "MXRA8-related_disorder|not_provided": 1,
    "CCNL2-related_disorder": 8,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7|Neuromuscular_disease|VWA1-related_disorder|not_provided": 1,
    "VWA1-related_disorder": 1,
    "Neuromuscular_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7|VWA1-related_disorder|Neuromuscular_disease": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7|not_specified": 1,
    "Neuromuscular_disease": 29,
    "Neuromuscular_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7": 7,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7": 3,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_7|not_provided": 2,
    "Harel-Yoon_syndrome|not_provided": 5,
    "Harel-Yoon_syndrome": 37,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Harel-Yoon_syndrome|not_specified|not_provided": 2,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|not_specified|Harel-Yoon_syndrome|not_provided": 1,
    "Harel-Yoon_syndrome|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal": 6,
    "Harel-Yoon_syndrome|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal": 8,
    "ATAD3A_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Harel-Yoon_syndrome|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal": 2,
    "not_provided|Harel-Yoon_syndrome": 2,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Harel-Yoon_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Harel-Yoon_syndrome": 3,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Harel-Yoon_syndrome|not_provided|Intellectual_disability": 1,
    "not_provided|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Harel-Yoon_syndrome": 3,
    "Inborn_genetic_diseases|Harel-Yoon_syndrome": 5,
    "Harel-Yoon_syndrome|Inborn_genetic_diseases": 1,
    "Disorder_of_development_or_morphogenesis": 3,
    "not_provided|Hearing_impairment": 47,
    "Harel-Yoon_syndrome|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|not_provided|not_specified": 1,
    "Congenital_cerebellar_hypoplasia|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal": 1,
    "Harel-Yoon_syndrome|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|not_provided": 3,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal": 1,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Inborn_genetic_diseases": 1,
    "not_provided|ATAD3A-related_condition": 1,
    "Intellectual_disability": 1458,
    "Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal|Harel-Yoon_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability": 9,
    "Harel-Yoon_syndrome|Inborn_genetic_diseases|Epilepsy|not_provided": 1,
    "Disorder_of_development_or_morphogenesis|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "not_provided|Harel-Yoon_syndrome|Pontocerebellar_hypoplasia|_hypotonia|_and_respiratory_insufficiency_syndrome|_neonatal_lethal": 1,
    "not_provided|Neurodevelopmental_disorder|Spinocerebellar_ataxia_type_21": 1,
    "Spinocerebellar_ataxia_type_21|not_provided": 3,
    "Spinocerebellar_ataxia_type_21": 4,
    "not_provided|Inborn_genetic_diseases|TMEM240-related_disorder": 1,
    "TMEM240-related_disorder|not_provided": 4,
    "not_provided|TMEM240-related_disorder": 3,
    "Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|TMEM240-related_disorder|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_type_21": 1,
    "Spinocerebellar_ataxia_type_21|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_21": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_21": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_21": 1,
    "TMEM240-related_disorder": 2,
    "not_provided|Spinocerebellar_ataxia_type_21|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified": 237,
    "Autosomal_recessive_osteopetrosis_4": 27,
    "Brachymorphism-onychodysplasia-dysphalangism_syndrome": 2,
    "Seizure": 156,
    "High_myopia": 44,
    "Intellectual_disability|_autosomal_dominant_42": 24,
    "Global_developmental_delay|Hypotonia|Bilateral_tonic-clonic_seizure|Intellectual_disability|Seizure|Intellectual_disability|_autosomal_dominant_42|Neurodevelopmental_Disability": 1,
    "Intellectual_disability|_autosomal_dominant_42|Myelodysplastic_syndrome|Acute_lymphoid_leukemia|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_42|not_provided": 5,
    "not_provided|GNB1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_42|Autosomal_dominant_non-syndromic_intellectual_disability": 1,
    "GNB1-related_disorder|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_42": 9,
    "Acute_lymphoid_leukemia|Intellectual_disability|_autosomal_dominant_42|Myelodysplastic_syndrome|not_provided": 1,
    "Myelodysplastic_syndrome|Intellectual_disability|_autosomal_dominant_42|Acute_lymphoid_leukemia|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_42|Inborn_genetic_diseases|not_provided": 1,
    "Dystonic_disorder|Atypical_behavior|Intellectual_disability|_autosomal_dominant_42|not_provided": 1,
    "See_cases|not_provided": 101,
    "Intellectual_disability|See_cases|not_provided": 1,
    "not_provided|Multifocal_epileptiform_discharges|Focal_impaired_awareness_seizure|Global_developmental_delay|Hypotonia|Bilateral_tonic-clonic_seizure|Developmental_regression|Expressive_language_delay|EEG_with_generalized_epileptiform_discharges|Intellectual_disability|Seizure|Intellectual_disability|_autosomal_dominant_42|Neurodevelopmental_Disability": 1,
    "Multifocal_epileptiform_discharges|Growth_delay|Global_developmental_delay|Hypotonia|Limb_hypertonia|Inability_to_walk|Feeding_difficulties|Expressive_language_delay|Strabismus|Cerebral_visual_impairment|Nystagmus|Intellectual_disability|Seizure|Failure_to_thrive|Intellectual_disability|_autosomal_dominant_42|not_provided|Neurodevelopmental_Disability|Microcephaly": 1,
    "Intellectual_disability|_autosomal_dominant_42|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_42|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_42|LEUKEMIA|_CHRONIC_LYMPHOCYTIC|_SOMATIC|Neurodevelopmental_abnormality|Infantile_axial_hypotonia|Cleft_palate|Dystonic_disorder|Growth_delay|Hypothyroidism|Upper_limb_hypertonia|Intellectual_disability|Neurodevelopmental_disorder|Inborn_genetic_diseases|not_specified|not_provided|Global_developmental_delay|Acute_lymphoid_leukemia|Myelodysplastic_syndrome|Limb_hypertonia|Inability_to_walk|Seizure|Hypotonia|Multifocal_epileptiform_discharges|EEG_with_generalized_epileptiform_discharges|Nystagmus|Expressive_language_delay|Developmental_regression|Strabismus|Failure_to_thrive|Cerebral_palsy|Neurodevelopmental_Disability|Neurodevelopmental_delay": 1,
    "not_provided|Multifocal_epileptiform_discharges|Growth_delay|Focal_impaired_awareness_seizure|Global_developmental_delay|Hypotonia|Limb_hypertonia|Feeding_difficulties|Floppy_infant|Cerebral_visual_impairment|Seizure|Failure_to_thrive|Acute_lymphoid_leukemia|Intellectual_disability|_autosomal_dominant_42|Neurodevelopmental_Disability": 1,
    "GNB1-related_disorder|Intellectual_disability|_autosomal_dominant_42|Inborn_genetic_diseases|not_provided|Floppy_infant|EEG_with_generalized_epileptiform_discharges|Hypotonia|Strabismus|Global_developmental_delay|Growth_delay|Seizure|Feeding_difficulties|Neurodevelopmental_Disability": 1,
    "Intellectual_disability|_autosomal_dominant_42|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_42|Intellectual_disability": 1,
    "Neurodevelopmental_delay|Intellectual_disability|_autosomal_dominant_42": 1,
    "not_provided|Autism_spectrum_disorder|Intellectual_disability|_autosomal_dominant_42|Neurodevelopmental_Disability|Hypotonia|Seizure|Global_developmental_delay|Inborn_genetic_diseases": 1,
    "Limb_hypertonia|Strabismus|Seizure|Failure_to_thrive|Focal_impaired_awareness_seizure|Global_developmental_delay|Neurodevelopmental_Disability|Hypotonia": 1,
    "Global_developmental_delay|Hypotonia|Floppy_infant|Intellectual_disability|Acute_lymphoid_leukemia|Intellectual_disability|_autosomal_dominant_42|not_provided|Neurodevelopmental_Disability|Seizure": 1,
    "Intellectual_disability|_autosomal_dominant_42|Acute_lymphoid_leukemia|Myelodysplastic_syndrome|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_42|not_provided|GNB1-related_disorder": 1,
    "GNB1-related_disorder": 3,
    "Ciliary_dyskinesia|_primary|_49|_without_situs_inversus": 10,
    "CFAP74-related_disorder": 2,
    "CFAP74-related_disorder|not_provided": 2,
    "Ciliary_dyskinesia|_primary|_49|_without_situs_inversus|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 31,
    "Idiopathic_generalized_epilepsy": 989,
    "Idiopathic_generalized_epilepsy|not_provided": 15,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_10|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_10": 18,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 19,
    "Idiopathic_generalized_epilepsy|GABRD-related_disorder|not_provided": 2,
    "not_provided|Idiopathic_generalized_epilepsy": 29,
    "GABRD-related_disorder|Idiopathic_generalized_epilepsy": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_10|Idiopathic_generalized_epilepsy|not_specified|not_provided": 1,
    "Idiopathic_generalized_epilepsy|GABRD-related_disorder": 6,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_10|Idiopathic_generalized_epilepsy": 3,
    "not_specified|not_provided|Idiopathic_generalized_epilepsy": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus_type_5": 1,
    "Idiopathic_generalized_epilepsy|not_specified": 18,
    "not_specified|Idiopathic_generalized_epilepsy": 16,
    "GABRD-related_disorder|not_specified|not_provided|Idiopathic_generalized_epilepsy|Generalized_epilepsy_with_febrile_seizures_plus_type_5": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_10|Idiopathic_generalized_epilepsy": 2,
    "Idiopathic_generalized_epilepsy|EEG_abnormality|GABRD-related_disorder|not_provided": 1,
    "not_specified|Idiopathic_generalized_epilepsy|not_provided": 3,
    "GABRD-related_disorder": 2,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_10": 4,
    "GABRD-related_disorder|not_specified|Idiopathic_generalized_epilepsy": 1,
    "Idiopathic_generalized_epilepsy|not_provided|not_specified": 1,
    "not_provided|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_10": 1,
    "Epileptic_encephalopathy|Idiopathic_generalized_epilepsy": 1,
    "GABRD-related_disorder|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "GABRD-related_disorder|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 2,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|not_provided": 2,
    "Intellectual_disability|not_provided|Idiopathic_generalized_epilepsy|GABRD-related_disorder": 1,
    "not_provided|GABRD-related_disorder|Idiopathic_generalized_epilepsy": 1,
    "GABRD-related_disorder|Inborn_genetic_diseases": 1,
    "Idiopathic_generalized_epilepsy|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "not_specified|See_cases|Idiopathic_generalized_epilepsy": 1,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_10": 1,
    "Shprintzen-Goldberg_syndrome": 405,
    "Shprintzen-Goldberg_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 15,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 114,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7389,
    "Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 18,
    "Shprintzen-Goldberg_syndrome|not_provided": 21,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 285,
    "Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 72,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Shprintzen-Goldberg_syndrome": 12,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 281,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Shprintzen-Goldberg_syndrome": 3,
    "Craniosynostosis_syndrome": 32,
    "Neurodevelopmental_abnormality": 112,
    "Inborn_genetic_diseases|Shprintzen-Goldberg_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Shprintzen-Goldberg_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Shprintzen-Goldberg_syndrome": 2,
    "Shprintzen-Goldberg_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 23,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 73,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|not_provided": 14,
    "SKI-related_disorder": 5,
    "not_provided|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "not_provided|Shprintzen-Goldberg_syndrome": 16,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 12,
    "See_cases|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Shprintzen-Goldberg_syndrome|not_specified": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 3,
    "not_specified|Shprintzen-Goldberg_syndrome": 7,
    "Shprintzen-Goldberg_syndrome|Intellectual_disability|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|SKI-related_disorder": 2,
    "Shprintzen-Goldberg_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SKI-related_disorder": 1,
    "SKI-related_disorder|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "SKI-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cardiovascular_phenotype|Shprintzen-Goldberg_syndrome": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 4,
    "Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|SKI-related_disorder": 1,
    "not_provided|Disproportionate_tall_stature": 1,
    "not_specified|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Shprintzen-Goldberg_syndrome|not_specified": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|not_specified": 2,
    "Shprintzen-Goldberg_syndrome|not_specified|not_provided": 1,
    "not_specified|Shprintzen-Goldberg_syndrome|SKI-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Shprintzen-Goldberg_syndrome|Autism_spectrum_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|SKI-related_disorder": 1,
    "Isolated_thoracic_aortic_aneurysm": 33,
    "not_provided|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Intellectual_disability|SKI-related_disorder": 1,
    "not_specified|Shprintzen-Goldberg_syndrome|not_provided": 2,
    "Shprintzen-Goldberg_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "SKI-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 3,
    "Isolated_thoracic_aortic_aneurysm|Shprintzen-Goldberg_syndrome": 1,
    "Shprintzen-Goldberg_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|not_provided|Shprintzen-Goldberg_syndrome": 1,
    "Isolated_thoracic_aortic_aneurysm|not_provided|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SKI-related_disorder": 1,
    "not_specified|Shprintzen-Goldberg_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 87,
    "Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_provided|Shprintzen-Goldberg_syndrome|Disproportionate_tall_stature": 1,
    "Shprintzen-Goldberg_syndrome|not_specified|SKI-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|SKI-related_disorder|Shprintzen-Goldberg_syndrome": 1,
    "Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SKI-related_disorder|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Shprintzen-Goldberg_syndrome": 1,
    "SKI-related_disorder|not_specified|not_provided|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Intellectual_disability|Shprintzen-Goldberg_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "SKI-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|not_provided": 1,
    "Shprintzen-Goldberg_syndrome|not_provided|not_specified": 1,
    "SKI-related_disorder|Arterial_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 1,
    "SKI-related_disorder|Shprintzen-Goldberg_syndrome": 2,
    "SKI-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "SKI-related_disorder|Shprintzen-Goldberg_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Shprintzen-Goldberg_syndrome|SKI-related_disorder": 1,
    "SKI-related_disorder|Shprintzen-Goldberg_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome|Intellectual_disability|not_provided": 1,
    "SKI-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Shprintzen-Goldberg_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 6,
    "Shprintzen-Goldberg_syndrome|SKI-related_disorder": 3,
    "not_specified|Shprintzen-Goldberg_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Disproportionate_tall_stature": 3,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)": 49,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)": 119,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided": 2,
    "not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 2,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B": 22,
    "Peroxisome_biogenesis_disorder|_complementation_group_7": 456,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 2,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|_complementation_group_7": 10,
    "not_provided|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7|Inborn_genetic_diseases|PEX10-related_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder": 7,
    "Zellweger_spectrum_disorders": 1277,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7": 13,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 3,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders": 14,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 11,
    "PEX10-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided": 2,
    "not_specified|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 10,
    "Zellweger_spectrum_disorders|PEX10-related_disorder|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Inborn_genetic_diseases": 1,
    "PEX10-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_7": 12,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 11,
    "Peroxisome_biogenesis_disorder_6B": 3,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|not_specified": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Inborn_genetic_diseases|Zellweger_spectrum_disorders|not_provided": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided": 2,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder": 1583,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_specified": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Inborn_genetic_diseases": 2,
    "not_provided|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|PEX10-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder": 1,
    "not_specified|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders|not_provided": 2,
    "not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided": 9,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided": 3,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Inborn_genetic_diseases": 6,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7": 6,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders": 1,
    "PEX10-related_disorder|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|PEX10-related_disorder|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_specified": 1,
    "Inborn_genetic_diseases|PEX10-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided": 2,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided|PEX10-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|PEX10-related_disorder": 1,
    "PEX10-related_disorder|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders|not_provided": 1,
    "PEX10-related_disorder": 5,
    "Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder": 2,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|_complementation_group_7": 2,
    "Zellweger_spectrum_disorders|not_specified": 8,
    "Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 2,
    "Inborn_genetic_diseases|Zellweger_spectrum_disorders": 11,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Spastic_ataxia": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|not_specified|PEX10-related_disorder": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Inborn_genetic_diseases|Zellweger_spectrum_disorders": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 2,
    "PEX10-related_disorder|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders|not_provided|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided": 2,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|not_provided": 1,
    "not_specified|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|PEX10-related_disorder": 1,
    "not_specified|Peroxisome_biogenesis_disorder|_complementation_group_7|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B": 2,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|PEX10-related_disorder": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder": 1,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "not_provided|Zellweger_spectrum_disorders|Inborn_genetic_diseases|PEX10-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|not_specified": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "PEX10-related_disorder|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|PEX10-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|not_provided|PEX10-related_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B": 1,
    "Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_6A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_6A_(Zellweger)|Peroxisome_biogenesis_disorder_6B|Peroxisome_biogenesis_disorder|_complementation_group_7": 1,
    "Cataract_49": 4,
    "Left_ventricular_noncompaction_8": 743,
    "not_provided|Left_ventricular_noncompaction_8": 77,
    "not_provided|Left_ventricular_noncompaction_8|not_specified": 19,
    "Left_ventricular_noncompaction_8|not_specified|not_provided": 20,
    "Left_ventricular_noncompaction_8|not_provided": 74,
    "not_provided|Inborn_genetic_diseases|Left_ventricular_noncompaction_8": 5,
    "not_specified|PRDM16-related_disorder|not_provided|Left_ventricular_noncompaction_8": 1,
    "Left_ventricular_noncompaction_8|Primary_dilated_cardiomyopathy|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Left_ventricular_noncompaction_8|not_provided": 13,
    "not_specified|Left_ventricular_noncompaction_8": 22,
    "Left_ventricular_noncompaction_8|not_specified": 36,
    "Left_ventricular_noncompaction_8|PRDM16-related_disorder": 3,
    "Left_ventricular_noncompaction_8|not_provided|PRDM16-related_disorder": 1,
    "PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Left_ventricular_noncompaction_8": 24,
    "Left_ventricular_noncompaction_8|Inborn_genetic_diseases": 24,
    "not_provided|Left_ventricular_noncompaction_8|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Left_ventricular_noncompaction_8|not_provided": 5,
    "not_provided|PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_specified": 4,
    "not_provided|not_specified|Left_ventricular_noncompaction_8": 6,
    "not_specified|not_provided|PRDM16-related_disorder|Left_ventricular_noncompaction_8": 2,
    "Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 104,
    "Left_ventricular_noncompaction_8|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Left_ventricular_noncompaction_8|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Left_ventricular_noncompaction_8|PRDM16-related_disorder": 1,
    "not_provided|PRDM16-related_disorder|Left_ventricular_noncompaction_8": 1,
    "PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_provided": 1,
    "Left_ventricular_noncompaction_8|not_provided|not_specified": 11,
    "PRDM16-related_disorder|Left_ventricular_noncompaction_8|Wolff-Parkinson-White_pattern|not_provided": 1,
    "not_provided|Left_ventricular_noncompaction_8|not_specified|PRDM16-related_disorder": 1,
    "PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_specified|not_provided": 5,
    "PRDM16-related_disorder|not_provided": 1,
    "Left_ventricular_noncompaction_8|Cardiomyopathy|_dilated|_1LL|Primary_dilated_cardiomyopathy": 1,
    "See_cases|Left_ventricular_noncompaction_8": 1,
    "not_provided|PRDM16-related_disorder|not_specified|Left_ventricular_noncompaction_8": 2,
    "Left_ventricular_noncompaction_8|not_specified|not_provided|PRDM16-related_disorder": 1,
    "Left_ventricular_noncompaction_cardiomyopathy": 17,
    "not_specified|Left_ventricular_noncompaction_8|not_provided|PRDM16-related_disorder": 1,
    "PRDM16-related_disorder|not_specified|Left_ventricular_noncompaction_8|not_provided": 2,
    "PRDM16-related_disorder": 4,
    "Left_ventricular_noncompaction_8|PRDM16-related_disorder|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Left_ventricular_noncompaction_8": 1,
    "PRDM16-related_disorder|Inborn_genetic_diseases|Left_ventricular_noncompaction_8|not_specified|not_provided": 1,
    "PRDM16-related_disorder|Left_ventricular_noncompaction_8": 4,
    "Left_ventricular_noncompaction_8|PRDM16-related_disorder|not_provided": 1,
    "Left_ventricular_noncompaction_8|not_provided|not_specified|PRDM16-related_disorder": 1,
    "not_provided|Left_ventricular_noncompaction_8|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Inborn_genetic_diseases|Left_ventricular_noncompaction_8|not_provided|not_specified": 1,
    "not_specified|not_provided|Left_ventricular_noncompaction_8": 4,
    "Wolff-Parkinson-White_pattern": 30,
    "PRDM16-related_disorder|not_provided|not_specified|Left_ventricular_noncompaction_8": 1,
    "not_provided|Left_ventricular_noncompaction_8|Inborn_genetic_diseases|not_specified": 1,
    "Primary_dilated_cardiomyopathy": 1335,
    "PRDM16-related_disorder|not_provided|Left_ventricular_noncompaction_8|not_specified": 1,
    "PRDM16-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Left_ventricular_noncompaction_8": 2,
    "not_provided|Inborn_genetic_diseases|PRDM16-related_disorder|Left_ventricular_noncompaction_8": 1,
    "Left_ventricular_noncompaction_8|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Inborn_genetic_diseases|not_specified|Left_ventricular_noncompaction_8": 1,
    "PRDM16-related_disorder|not_provided|Left_ventricular_noncompaction_8": 1,
    "Inborn_genetic_diseases|PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_specified|not_provided": 2,
    "not_specified|not_provided|Left_ventricular_noncompaction_8|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_8|Primary_dilated_cardiomyopathy": 1,
    "Familial_restrictive_cardiomyopathy": 2,
    "Left_ventricular_noncompaction_8|Familial_restrictive_cardiomyopathy": 1,
    "not_specified|PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_provided": 2,
    "PRDM16-related_disorder|Inborn_genetic_diseases|not_specified|Left_ventricular_noncompaction_8|not_provided": 1,
    "PRDM16-related_disorder|not_specified|not_provided|Left_ventricular_noncompaction_8": 1,
    "PRDM16-related_disorder|not_provided|Inborn_genetic_diseases|Left_ventricular_noncompaction_8": 1,
    "Cardiomyopathy|_dilated|_1LL": 1,
    "Wolff-Parkinson-White_pattern|Left_ventricular_noncompaction_8|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_8|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|Left_ventricular_noncompaction_8": 1,
    "not_provided|PRDM16-related_disorder|Inborn_genetic_diseases|Left_ventricular_noncompaction_8|not_specified": 1,
    "Left_ventricular_noncompaction_8|not_specified|not_provided|Microcephaly|PRDM16-related_disorder": 1,
    "Wolff-Parkinson-White_pattern|Left_ventricular_noncompaction_8|not_provided": 1,
    "PRDM16-related_congenital_heart_disease|Left_ventricular_noncompaction_8": 1,
    "not_provided|Left_ventricular_noncompaction_8|Primary_dilated_cardiomyopathy": 1,
    "Inborn_genetic_diseases|Left_ventricular_noncompaction_8|PRDM16-related_disorder": 1,
    "PRDM16-related_disorder|Left_ventricular_noncompaction_8|Cardiomyopathy|_dilated|_1LL|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_8|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|PRDM16-related_disorder|Left_ventricular_noncompaction_8|not_provided": 1,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma": 503,
    "Ciliary_dyskinesia|_primary|_47|_and_lissencephaly": 12,
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    "Vel_blood_group_system": 1,
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    "not_provided|Joubert_syndrome_25": 18,
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    "not_provided|Joubert_syndrome_25|Inborn_genetic_diseases": 2,
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    "Joubert_syndrome_25|not_provided": 16,
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    "not_specified|Joubert_syndrome_25|Inborn_genetic_diseases|not_provided": 1,
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    "Joubert_syndrome_and_related_disorders": 60,
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    "Joubert_syndrome_25|Intellectual_developmental_disorder|_autosomal_recessive_77|Joubert_syndrome_and_related_disorders": 2,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_25": 1,
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    "Joubert_syndrome_25|Inborn_genetic_diseases|not_provided": 2,
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    "Joubert_syndrome_25|not_specified": 1,
    "Joubert_syndrome_25|not_provided|CEP104-related_disorder": 2,
    "not_provided|Joubert_syndrome_25|CEP104-related_disorder": 3,
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    "Joubert_syndrome|Inborn_genetic_diseases": 27,
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    "Joubert_syndrome_25|Intellectual_developmental_disorder|_autosomal_recessive_77|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_25|not_provided|not_specified": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_25|not_provided": 1,
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    "Intellectual_developmental_disorder|_autosomal_recessive_77|Joubert_syndrome_and_related_disorders": 1,
    "not_specified|not_provided|Joubert_syndrome_25": 2,
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    "Intellectual_developmental_disorder|_autosomal_recessive_77|not_provided|Joubert_syndrome_25": 1,
    "Joubert_syndrome_25|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_25|Intellectual_developmental_disorder|_autosomal_recessive_77|not_provided": 1,
    "Cerebellar_ataxia|Dystonic_disorder|Global_developmental_delay": 1,
    "not_specified|Joubert_syndrome_25|Inborn_genetic_diseases": 1,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4": 5,
    "Senior-Loken_syndrome_4|Nephronophthisis_4": 25,
    "Nephronophthisis": 2710,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4": 47,
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    "Nephronophthisis_4": 24,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Nephronophthisis": 7,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_specified|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|not_provided": 97,
    "Retinal_dystrophy|Nephronophthisis": 1,
    "not_provided|Nephronophthisis": 66,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis|not_provided|NPHP4-related_disorder": 4,
    "NPHP4-related_disorder|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|Retinal_dystrophy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis": 63,
    "NPHP4-related_disorder|not_provided|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 1,
    "Nephronophthisis|NPHP4-related_disorder|not_provided": 6,
    "Nephronophthisis_4|Senior-Loken_syndrome_4": 90,
    "Nephronophthisis_4|NPHP4-related_disorder|Nephronophthisis|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 5,
    "Retinal_dystrophy|not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_provided": 6,
    "Inborn_genetic_diseases|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 4,
    "NPHP4-related_disorder|Nephronophthisis": 24,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|Inborn_genetic_diseases|not_provided|Nephronophthisis": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 22,
    "Nephronophthisis|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4": 4,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4": 21,
    "Nephronophthisis|Inborn_genetic_diseases|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 3,
    "Nephronophthisis|NPHP4-related_disorder": 24,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|NPHP4-related_disorder": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 26,
    "Nephronophthisis|not_provided|Inborn_genetic_diseases|NPHP4-related_disorder": 3,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder": 3,
    "Nephronophthisis|not_provided|not_specified|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 4,
    "not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 5,
    "Nephronophthisis|not_provided|NPHP4-related_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Inborn_genetic_diseases|Nephronophthisis_4|Senior-Loken_syndrome_4": 5,
    "NPHP4-related_disorder|not_provided|Nephronophthisis": 7,
    "Nephronophthisis|Kidney_disorder": 1,
    "Nephronophthisis|Inborn_genetic_diseases": 32,
    "NPHP4-related_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4|not_specified|not_provided|Nephronophthisis": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Inborn_genetic_diseases|NPHP4-related_disorder|Nephronophthisis|not_provided": 1,
    "NPHP4-related_disorder|Nephronophthisis|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 5,
    "not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|Inborn_genetic_diseases": 1,
    "Kidney_disorder|Nephronophthisis|not_provided|not_specified|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|not_provided": 13,
    "Nephronophthisis|not_provided|Nephronophthisis_4": 3,
    "Nephronophthisis|not_specified|not_provided": 6,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 3,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided|NPHP4-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis_4|Nephronophthisis": 2,
    "Senior-Loken_syndrome_4|Nephronophthisis|Nephronophthisis_4": 3,
    "NPHP4-related_disorder|Nephronophthisis|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4": 2,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases|Nephronophthisis|not_provided": 2,
    "Nephronophthisis|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis_4": 1,
    "Nephronophthisis|Inborn_genetic_diseases|NPHP4-related_disorder": 1,
    "Nephronophthisis|Retinal_dystrophy": 2,
    "Nephronophthisis_4|Nephronophthisis|NPHP4-related_disorder|Senior-Loken_syndrome_4|not_provided": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases|Nephronophthisis|Retinal_dystrophy": 1,
    "Nephronophthisis|Inborn_genetic_diseases|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Incidental_Discovery": 13,
    "Kidney_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases": 8,
    "not_specified|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|Retinal_dystrophy|Kidney_disorder": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|Inborn_genetic_diseases": 4,
    "not_provided|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis|Nephronophthisis_4": 1,
    "NPHP4-related_disorder|Nephronophthisis|not_specified|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 1,
    "Nephronophthisis|not_specified|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4": 7,
    "not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis|not_provided|Senior-Loken_syndrome_4": 1,
    "Senior-Loken_syndrome_4": 3,
    "Nephronophthisis|not_specified|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|Focal_segmental_glomerulosclerosis": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis": 4,
    "Nephronophthisis|not_specified": 9,
    "Nephronophthisis|Nephronophthisis_4": 6,
    "Nephronophthisis|not_specified|Bardet-Biedl_syndrome": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_provided": 7,
    "Nephronophthisis|Inborn_genetic_diseases|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "NPHP4-related_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided|Nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4": 2,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Retinal_dystrophy|NPHP4-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis|not_provided|Inborn_genetic_diseases|Nephronophthisis_4|Senior-Loken_syndrome_4": 2,
    "Nephronophthisis|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4": 8,
    "Kidney_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_specified|not_provided": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases": 4,
    "Nephronophthisis|Nephronophthisis_4|not_provided|Senior-Loken_syndrome_4": 1,
    "NPHP4-related_disorder|Nephronophthisis_4|Nephronophthisis|Senior-Loken_syndrome_4|not_provided": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Retinal_dystrophy|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|NPHP4-related_disorder|Inborn_genetic_diseases": 1,
    "NPHP4-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 1,
    "Kidney_disorder|Nephronophthisis|not_provided|not_specified|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "NPHP4-related_disorder|Nephronophthisis|not_provided": 5,
    "not_provided|Nephronophthisis_4|not_specified": 1,
    "not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis": 2,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified|not_provided": 1,
    "NPHP4-related_disorder|Nephronophthisis|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 2,
    "Nephronophthisis_4|not_specified|Senior-Loken_syndrome_4|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|not_provided|NPHP4-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis|not_specified|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 2,
    "not_provided|NPHP4-related_disorder|Nephronophthisis|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Retinal_dystrophy|Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|Nephronophthisis|not_provided": 1,
    "NPHP4-related_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 2,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_provided|NPHP4-related_disorder": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 6,
    "not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4": 5,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|NPHP4-related_disorder|not_provided|not_specified": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Nephronophthisis": 9,
    "Nephronophthisis_4|Nephronophthisis|not_specified|Senior-Loken_syndrome_4": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified|Nephronophthisis": 1,
    "not_provided|NPHP4-related_disorder|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases": 1,
    "NPHP4-related_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis": 3,
    "Nephronophthisis|not_specified|not_provided|NPHP4-related_disorder": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|not_provided|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_specified|not_provided": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|Nephronophthisis": 3,
    "Kidney_disorder|not_provided|Nephronophthisis": 1,
    "not_specified|not_provided|Nephronophthisis|NPHP4-related_disorder|Inborn_genetic_diseases": 1,
    "Kidney_disorder|Cholestasis|Nephronophthisis|not_specified|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis_4|not_provided|Kidney_disorder|Nephronophthisis|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_specified": 1,
    "NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis|not_provided": 1,
    "NPHP4-related_disorder|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4": 4,
    "not_provided|Nephronophthisis_4|Nephronophthisis|not_specified|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Inborn_genetic_diseases|Nephronophthisis": 2,
    "not_specified|not_provided|Nephronophthisis": 2,
    "not_provided|not_specified|Nephronophthisis": 2,
    "not_specified|Nephronophthisis|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "not_provided|Nephronophthisis|NPHP4-related_disorder": 4,
    "NPHP4-related_disorder|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis|Nephronophthisis_4|not_specified|Senior-Loken_syndrome_4|not_provided": 1,
    "NPHP4-related_disorder|not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4": 4,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases|Nephronophthisis": 3,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Nephronophthisis|Inborn_genetic_diseases|NPHP4-related_disorder|Nephronophthisis_4": 1,
    "Kidney_disorder|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified|not_provided": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided|Nephronophthisis": 2,
    "Nephronophthisis|not_provided|not_specified|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|not_provided|Inborn_genetic_diseases|NPHP4-related_disorder": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|NPHP4-related_disorder|Nephronophthisis": 1,
    "NPHP4-related_disorder|Inborn_genetic_diseases|not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Nephronophthisis|Inborn_genetic_diseases|Nephronophthisis_4|Senior-Loken_syndrome_4": 5,
    "Nephronophthisis_4|Nephronophthisis|Senior-Loken_syndrome_4|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "not_provided|not_specified|Nephronophthisis_4": 2,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|not_provided": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified": 3,
    "Kidney_disorder|Nephronophthisis|not_specified|not_provided|Nephronophthisis_4": 1,
    "not_provided|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis_4|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Inborn_genetic_diseases": 1,
    "CHARGE_syndrome": 2307,
    "not_provided|Retinal_dystrophy|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "not_specified|Inborn_genetic_diseases|NPHP4-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis|Inborn_genetic_diseases|not_provided": 7,
    "Nephronophthisis|NPHP4-related_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Optic_atrophy": 125,
    "not_provided|Leber_congenital_amaurosis": 27,
    "Nephronophthisis|Senior-Loken_syndrome_4": 1,
    "not_provided|NPHP4-related_disorder|Nephronophthisis": 5,
    "not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|Kidney_disorder|Nephronophthisis": 1,
    "NPHP4-related_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 2,
    "Nephronophthisis|not_specified|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Bardet-Biedl_syndrome": 4373,
    "Inborn_genetic_diseases|Nephronophthisis|Retinal_dystrophy": 2,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided|NPHP4-related_disorder|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|Kidney_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified": 1,
    "NPHP4-related_disorder|not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|not_specified|Atypical_hemolytic-uremic_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|Kidney_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Leber_congenital_amaurosis|not_provided|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Bardet-Biedl_syndrome": 1,
    "not_provided|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis_4|Nephronophthisis": 1,
    "NPHP4-related_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Infertility_disorder|Cerebello-oculo-renal_syndrome_(nephronophthisis|_oculomotor_apraxia_and_cerebellar_abnormalities)|Nephronophthisis|Nephronophthisis_4": 1,
    "not_provided|Nephronophthisis_4|Inborn_genetic_diseases|NPHP4-related_disorder|Nephronophthisis|Senior-Loken_syndrome_4": 1,
    "not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|NPHP4-related_disorder": 1,
    "Nephronophthisis|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "not_provided|not_specified|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis|not_provided": 1,
    "NPHP4-related_disorder|not_specified|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 1,
    "NPHP4-related_disorder|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 1,
    "Nephronophthisis|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_specified": 2,
    "Nephronophthisis|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified": 1,
    "NPHP4-related_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4|Bardet-Biedl_syndrome|Nephronophthisis|not_provided": 1,
    "not_provided|NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis": 1,
    "not_specified|not_provided|Kidney_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis": 1,
    "Inborn_genetic_diseases|NPHP4-related_disorder|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 1,
    "not_specified|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|not_provided": 2,
    "Nephronophthisis|not_specified|Kidney_disorder|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "not_specified|Lynch_syndrome_1|NPHP4-related_disorder|Nephronophthisis|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Kidney_disorder|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided|not_specified": 1,
    "not_provided|Kidney_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Nephronophthisis|not_specified": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|NPHP4-related_disorder|not_provided": 2,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|not_specified|Nephronophthisis": 1,
    "not_provided|Kidney_disorder|Nephronophthisis|not_specified|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified|Nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis_4|not_specified|Nephronophthisis|not_provided|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis|Nephronophthisis_4|not_provided|focal_and_segmental_glomerulosclerosis|Renal_dysplasia_and_retinal_aplasia": 1,
    "NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|NPHP4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|Inborn_genetic_diseases": 2,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|NPHP4-related_disorder|Retinal_dystrophy": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder": 2,
    "Nephronophthisis|Nephronophthisis_4|not_provided": 1,
    "Kidney_disorder|Nephronophthisis|not_provided|Senior-Loken_syndrome_4|NPHP4-related_disorder|Nephronophthisis_4|not_specified": 1,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis|Nephronophthisis_4|not_specified": 1,
    "not_provided|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases": 2,
    "not_specified|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|NPHP4-related_disorder": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|not_provided|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Inborn_genetic_diseases|not_provided|Nephronophthisis": 5,
    "Nephronophthisis|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|NPHP4-related_disorder": 1,
    "Nephronophthisis|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|NPHP4-related_disorder|Inborn_genetic_diseases": 1,
    "NPHP4-related_disorder|Nephronophthisis|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_provided|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Retinal_dystrophy|Nephronophthisis|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided": 1,
    "Nephronophthisis|Retinal_dystrophy|Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Senior-Loken_syndrome_4|Ciliopathy|Inborn_genetic_diseases|Nephronophthisis_4": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Retinal_dystrophy|not_provided|NPHP4-related_disorder|Nephronophthisis": 1,
    "not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4": 2,
    "NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis": 1,
    "Nephronophthisis|Inborn_genetic_diseases|not_provided|NPHP4-related_disorder|Nephronophthisis_4|Senior-Loken_syndrome_4": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "Nephronophthisis|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Nephronophthisis|not_specified|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "NPHP4-related_disorder|Nephronophthisis|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified|not_provided": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|NPHP4-related_disorder|Kidney_disorder|Optic_atrophy|Retinal_dystrophy|Inborn_genetic_diseases|Nephronophthisis|not_provided": 1,
    "NPHP4-related_disorder|Inborn_genetic_diseases|Nephronophthisis|not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "Senior-Loken_syndrome_4|Nephronophthisis_4|Nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "Kidney_disorder|not_specified|Renal_dysplasia_and_retinal_aplasia|Nephronophthisis_4|Senior-Loken_syndrome_4|not_provided|Nephronophthisis": 1,
    "Senior-Loken_syndrome_4|Retinal_dystrophy|NPHP4-related_disorder|Nephronophthisis|Nephronophthisis_4|not_provided": 1,
    "not_provided|Senior-Loken_syndrome_4|Nephronophthisis_4|not_specified": 1,
    "Nephronophthisis|not_specified|not_provided|Kidney_disorder|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_4|Senior-Loken_syndrome_4|Inborn_genetic_diseases": 1,
    "Nephronophthisis_4|Senior-Loken_syndrome_4|Kidney_disorder|Nephronophthisis": 1,
    "NPHP4-related_disorder|Nephronophthisis|Retinal_dystrophy|Senior-Loken_syndrome_4|Nephronophthisis_4": 1,
    "not_provided|NPHP4-related_disorder": 1,
    "Renal_dysplasia_and_retinal_aplasia|Nephronophthisis": 4,
    "KCNAB2-related_disorder": 10,
    "KCNAB2-related_epilepsy|not_specified": 1,
    "not_provided|KCNAB2-related_disorder": 5,
    "KCNAB2-related_disorder|not_provided": 3,
    "KCNAB2-related_disorder|not_specified|not_provided": 1,
    "Parenti-mignot_neurodevelopmental_syndrome": 51,
    "CHD5-related_disorder": 20,
    "CHD5-related_disorder|not_provided": 5,
    "Parenti-mignot_neurodevelopmental_syndrome|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder|CHD5-related_disorder": 1,
    "CHD5-related_Neurodevelopmental_disorder": 1,
    "Global_developmental_delay|Seizure|Intellectual_disability": 2,
    "Parenti-mignot_neurodevelopmental_syndrome|not_provided": 3,
    "Global_developmental_delay|Seizure|Intellectual_disability|not_provided": 3,
    "Parenti-mignot_neurodevelopmental_syndrome|Global_developmental_delay|Intellectual_disability": 1,
    "Neurodevelopmental_delay": 137,
    "Seizure|Parenti-mignot_neurodevelopmental_syndrome": 1,
    "Global_developmental_delay|Seizure": 4,
    "CHD5-related_disorder|Inborn_genetic_diseases": 1,
    "Seizure|CHD5-related_disorder": 1,
    "CHD5-associated_Neurodevelopmental_disorder": 1,
    "Global_developmental_delay|Intellectual_disability|not_provided": 1,
    "not_provided|CHD5-related_disorder": 2,
    "Inborn_genetic_diseases|Parenti-mignot_neurodevelopmental_syndrome": 2,
    "Global_developmental_delay": 90,
    "Seizure|not_provided|Parenti-mignot_neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Intellectual_disability": 3,
    "Parenti-mignot_neurodevelopmental_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Seizure|Parenti-mignot_neurodevelopmental_syndrome": 1,
    "not_provided|Parenti-mignot_neurodevelopmental_syndrome|Global_developmental_delay|Intellectual_disability": 1,
    "Long_QT_syndrome": 5805,
    "Childhood-onset_schizophrenia": 18,
    "ACOT7-related_disorder": 6,
    "Usher_syndrome|_type_1M|Autosomal_recessive_nonsyndromic_hearing_loss_36|not_provided": 1,
    "Rare_genetic_deafness": 168,
    "Autosomal_recessive_nonsyndromic_hearing_loss_28": 58,
    "not_provided|Retinal_dystrophy|Inborn_genetic_diseases": 28,
    "Inborn_genetic_diseases|not_specified": 502,
    "ESPN-related_disorder|not_provided": 7,
    "not_provided|ESPN-related_disorder": 4,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 76,
    "not_provided|not_specified|ESPN-related_disorder": 1,
    "Usher_syndrome|_type_1M|Autosomal_recessive_nonsyndromic_hearing_loss_36": 1,
    "Sensorineural_hearing_loss_disorder": 21,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases": 71,
    "Usher_syndrome|_type_1M|Retinal_dystrophy|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|not_specified|not_provided": 1,
    "ESPN-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Usher_syndrome|_type_1M|Autosomal_recessive_nonsyndromic_hearing_loss_36": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Usher_syndrome|_type_1M|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Usher_syndrome|_type_1M": 1,
    "ESPN-related_disorder": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_36|Usher_syndrome|_type_1M": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_36": 2,
    "not_provided|Inborn_genetic_diseases|ESPN-related_disorder": 2,
    "not_provided|ESPN-related_disorder|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36": 14,
    "Deafness|_autosomal_recessive_36|_without_vestibular_involvement": 1,
    "ESPN-related_disorder|Usher_syndrome|_type_1M|Autosomal_recessive_nonsyndromic_hearing_loss_36|not_provided": 1,
    "not_provided|ESPN-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Usher_syndrome|_type_1M|not_provided": 1,
    "ESPN-related_disorder|Usher_syndrome|_type_1M|Autosomal_recessive_nonsyndromic_hearing_loss_36|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided": 234,
    "Inborn_genetic_diseases|Sensorineural_hearing_loss_disorder|not_provided": 1,
    "Deafness|_without_vestibular_involvement|_autosomal_dominant": 2,
    "not_specified|not_provided|Inborn_genetic_diseases": 264,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Usher_syndrome|_type_1M|Deafness|_without_vestibular_involvement|_autosomal_dominant|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_36|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1|Usher_syndrome|_type_1M": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_36|Hearing_loss|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_specified|not_provided": 448,
    "Deafness|_without_vestibular_involvement|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_36": 1,
    "TNFRSF25-related_disorder": 8,
    "TNFRSF25-related_disorder|not_provided": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 11,
    "Distal_spinal_muscular_atrophy": 34,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 40,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 569,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 274,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 11,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 35,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 20,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|Inborn_genetic_diseases": 7,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 2,
    "PLEKHG5-related_disorder|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 1,
    "not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 5,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided": 19,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases": 16,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C": 5,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|not_provided": 3,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided": 22,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases": 20,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|not_provided": 7,
    "Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases|not_provided": 6,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 20,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided": 12,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 4,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 2,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|not_provided": 1,
    "PLEKHG5-related_disorder|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 6,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|not_specified": 3,
    "not_provided|PLEKHG5-related_disorder|Inborn_genetic_diseases|not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided": 8,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified": 8,
    "Inborn_genetic_diseases|not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 2,
    "not_specified|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|Inborn_genetic_diseases": 1,
    "PLEKHG5-related_disorder|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 3,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases": 1,
    "Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 7,
    "not_provided|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases": 1,
    "Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 1,
    "not_specified|Distal_spinal_muscular_atrophy|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "not_provided|not_specified|PLEKHG5-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|not_provided": 3,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 8,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|PLEKHG5-related_disorder": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided": 1,
    "Hereditary_motor_neuron_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 1,
    "not_provided|PLEKHG5-related_disorder|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Juvenile_amyotrophic_lateral_sclerosis": 5,
    "not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided": 1,
    "PLEKHG5-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|not_specified": 2,
    "PLEKHG5-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|Inborn_genetic_diseases|PLEKHG5-related_disorder|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|PLEKHG5-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|PLEKHG5-related_disorder": 2,
    "not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 3,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|PLEKHG5-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|PLEKHG5-related_disorder|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided": 1,
    "Hereditary_spastic_paraplegia": 458,
    "PLEKHG5-related_disorder|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|not_provided": 1,
    "not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|PLEKHG5-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Inborn_genetic_diseases|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|PLEKHG5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PLEKHG5-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|not_provided|PLEKHG5-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|PLEKHG5-related_disorder|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Inborn_genetic_diseases|PLEKHG5-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 1,
    "not_specified|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|PLEKHG5-related_disorder|not_provided": 1,
    "Testicular_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_C|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Spinal_muscular_atrophy|_facioscapulohumeral_type": 1,
    "Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|PLEKHG5-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|Charcot-Marie-Tooth_disease_recessive_intermediate_C": 1,
    "Charcot-Marie-Tooth_disease": 712,
    "PLEKHG5-related_disorder": 2,
    "PLEKHG5-related_disorder|not_provided": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4|not_specified|not_provided": 1,
    "not_provided|not_specified|PLEKHG5-related_disorder|Peripheral_neuropathy": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_C|not_provided|not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_4": 1,
    "KLHL21-related_disorder": 9,
    "Ependymoma": 32,
    "CAMTA1-related_disorder": 28,
    "not_provided|Neurodevelopmental_abnormality": 7,
    "not_provided|CAMTA1-related_disorder": 8,
    "Developmental_disorder": 142,
    "CAMTA1-related_disorder|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 2,
    "Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|not_provided": 13,
    "not_provided|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 17,
    "not_specified|not_provided|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 3,
    "Inborn_genetic_diseases|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 3,
    "Intellectual_disability|not_provided|Inborn_genetic_diseases": 8,
    "CAMTA1-related_disorder|not_provided": 13,
    "Epilepsy|CAMTA1-related_disorder": 1,
    "Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|not_provided|Inborn_genetic_diseases": 3,
    "Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 2,
    "Inborn_genetic_diseases|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|not_provided": 1,
    "CAMTA1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|CAMTA1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities": 132,
    "Intellectual_disability|not_provided": 111,
    "Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|not_provided|not_specified": 1,
    "not_provided|Intellectual_disability|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 1,
    "Hereditary_ataxia": 25,
    "not_provided|Inborn_genetic_diseases|Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities": 1,
    "Cerebellar_dysfunction_with_variable_cognitive_and_behavioral_abnormalities|not_specified": 1,
    "PER3-related_disorder": 15,
    "Advanced_sleep_phase_syndrome_3": 4,
    "not_specified|not_provided|Advanced_sleep_phase_syndrome_3": 2,
    "Advanced_sleep_phase_syndrome": 1,
    "PER3-related_disorder|not_provided": 2,
    "not_specified|Advanced_sleep_phase_syndrome_3": 1,
    "not_provided|PER3-related_disorder": 3,
    "PER3-related_disorder|Advanced_sleep_phase_syndrome_3|not_provided": 1,
    "not_specified|PER3-related_disorder|not_provided": 1,
    "PER3-related_disorder|not_specified": 1,
    "Methylcobalamin_deficiency_type_cblE": 671,
    "Immunodeficiency_109_with_lymphoproliferation|not_provided": 2,
    "not_provided|TNFRSF9-related_disorder": 3,
    "TNFRSF9-related_disorder|not_provided": 2,
    "Immunodeficiency_109_with_lymphoproliferation": 1,
    "not_provided|TNFRSF9-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Parkinson_Disease|_Recessive": 3,
    "Parkinson_Disease|_Recessive": 9,
    "Autosomal_recessive_early-onset_Parkinson_disease_7|not_provided": 9,
    "Autosomal_recessive_early-onset_Parkinson_disease_7": 61,
    "PARK7-related_disorder": 1,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_7|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_early-onset_Parkinson_disease_7": 1,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_7": 4,
    "Parkinson_disease|_autosomal_recessive_early-onset|_digenic|_PINK1/DJ1": 2,
    "Amyotrophic_lateral_sclerosis-parkinsonism-dementia_complex": 6,
    "not_specified|not_provided|Autosomal_recessive_early-onset_Parkinson_disease_7": 1,
    "Parkinson_Disease|_Recessive|Autosomal_recessive_early-onset_Parkinson_disease_7|not_provided|not_specified": 1,
    "not_specified|Renal_cysts_and_diabetes_syndrome|PARK7-related_disorder|Autosomal_recessive_early-onset_Parkinson_disease_7|not_provided": 1,
    "Juvenile-onset_Parkinson_disease|Motor_neuron_disease": 1,
    "Parkinson_disease|_late-onset": 59,
    "not_specified|Autosomal_recessive_early-onset_Parkinson_disease_7": 1,
    "Young-onset_Parkinson_disease": 7,
    "not_provided|not_specified|Autosomal_recessive_early-onset_Parkinson_disease_7": 1,
    "SLC45A1-related_disorder": 11,
    "Intellectual_developmental_disorder_with_neuropsychiatric_features|not_specified": 4,
    "Intellectual_developmental_disorder_with_neuropsychiatric_features": 12,
    "not_provided|SLC45A1-related_disorder": 2,
    "not_specified|SLC45A1-related_disorder": 1,
    "SLC45A1-related_disorder|not_provided": 1,
    "not_specified|Intellectual_developmental_disorder_with_neuropsychiatric_features": 2,
    "Intellectual_developmental_disorder_with_neuropsychiatric_features|not_provided|SLC45A1-related_disorder": 1,
    "Intellectual_developmental_disorder_with_neuropsychiatric_features|not_provided": 3,
    "not_provided|Intellectual_developmental_disorder_with_neuropsychiatric_features": 1,
    "SLC45A1-related_disorder|Intellectual_developmental_disorder_with_neuropsychiatric_features": 1,
    "SLC45A1-related_disorder|Intellectual_developmental_disorder_with_neuropsychiatric_features|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 108,
    "Inborn_genetic_diseases|RERE-related_disorder": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 9,
    "RERE-related_disorder": 25,
    "RERE-related_disorder|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided": 2,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided": 16,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided|CHARGE_syndrome": 1,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|Cerebral_visual_impairment_and_intellectual_disability|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 11,
    "not_provided|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|Inborn_genetic_diseases": 3,
    "not_provided|RERE-related_disorder": 13,
    "Inborn_genetic_diseases|RERE-related_disorder|not_provided": 2,
    "RERE-related_disorder|not_provided": 11,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|Neurodevelopmental_disorder|not_provided": 1,
    "RERE-related_disorder|not_provided|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 2,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 2,
    "RERE-related_disorder|not_provided|not_specified": 1,
    "See_cases|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided|RERE-related_disorder|Inborn_genetic_diseases": 1,
    "RERE-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 1,
    "RERE-related_disorder|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 1,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart": 1,
    "Cleft_palate|Inborn_genetic_diseases": 2,
    "not_provided|See_cases": 131,
    "RERE-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|RERE-related_disorder": 1,
    "Developmental_disorder|Inborn_genetic_diseases": 4,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|RERE-related_disorder": 1,
    "Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|not_provided|RERE-related_disorder": 1,
    "RERE-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|RERE-related_disorder|Neurodevelopmental_disorder_with_or_without_anomalies_of_the_brain|_eye|_or_heart|Intellectual_disability": 1,
    "not_specified|Cortisone_reductase_deficiency_1": 1,
    "Cortisone_reductase_deficiency_1": 6,
    "not_provided|H6PD-related_disorder": 4,
    "Cortisone_reductase_deficiency_1|not_provided": 4,
    "not_provided|Cortisone_reductase_deficiency_1|not_specified": 1,
    "H6PD-related_disorder|not_provided": 4,
    "not_provided|Cortisone_reductase_deficiency_1": 4,
    "Inborn_genetic_diseases|Cortisone_reductase_deficiency_1": 1,
    "Cortisone_reductase_deficiency_1|Inborn_genetic_diseases": 1,
    "H6PD-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "SLC25A33-related_disorder": 5,
    "Immunodeficiency_14": 682,
    "Immunodeficiency_14|Activated_PI3K-delta_syndrome": 14,
    "not_provided|Inborn_genetic_diseases|Immunodeficiency_14": 2,
    "Immunodeficiency_14|not_provided": 34,
    "PIK3CD-related_disorder|Inborn_genetic_diseases|Immunodeficiency_14": 1,
    "Immunodeficiency_14|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14b|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Immunodeficiency_14": 9,
    "Immunodeficiency_14|not_provided|Inborn_genetic_diseases": 2,
    "Immunodeficiency_14b|_autosomal_recessive|Immunodeficiency_14": 1,
    "PIK3CD-related_disorder": 3,
    "Immunodeficiency_14|Inborn_genetic_diseases": 12,
    "Immunodeficiency_14b|_autosomal_recessive": 4,
    "Immunodeficiency_14|PIK3CD-related_disorder": 7,
    "Immunodeficiency_14|not_specified": 6,
    "not_provided|Immunodeficiency_14": 20,
    "Immunodeficiency_14|not_specified|not_provided": 2,
    "not_provided|PIK3CD-related_disorder|Inborn_genetic_diseases|Immunodeficiency_14": 1,
    "Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Activated_PI3K-delta_syndrome|not_provided": 1,
    "PIK3CD-related_disorder|Immunodeficiency_14": 9,
    "Inborn_genetic_diseases|Immunodeficiency_14|not_provided|Activated_PI3K-delta_syndrome": 1,
    "not_provided|not_specified|Immunodeficiency_14": 1,
    "See_cases|not_provided|Immunodeficiency_14|Activated_PI3K-delta_syndrome": 1,
    "Activated_PI3K-delta_syndrome|Immunodeficiency_14": 3,
    "not_specified|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive|PIK3CD-related_disorder|not_provided": 1,
    "PIK3CD-related_disorder|Immunodeficiency_14|not_provided": 2,
    "PIK3CD-related_disorder|Activated_PI3K-delta_syndrome|Immunodeficiency_14": 1,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency_14|not_specified": 1,
    "Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive|not_provided": 2,
    "not_provided|Activated_PI3K-delta_syndrome": 1,
    "Inborn_genetic_diseases|Immunodeficiency_14|not_provided": 1,
    "Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|not_provided": 1,
    "not_provided|Immunodeficiency_14|not_specified|PIK3CD-related_disorder": 1,
    "Immunodeficiency_14|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14b|_autosomal_recessive|PIK3CD-related_disorder|not_provided": 1,
    "PIK3CD-related_disorder|Immunodeficiency_14|Activated_PI3K-delta_syndrome": 1,
    "Immunodeficiency_14|not_specified|Inborn_genetic_diseases": 1,
    "Abnormality_of_the_immune_system|not_provided|Immunodeficiency_14": 1,
    "Activated_PI3K-delta_syndrome": 4,
    "Immunodeficiency_14|Inborn_genetic_diseases|not_provided|See_cases|PIK3CD-related_disorder|Immunodeficiency_14b|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency_14": 1,
    "Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive|not_specified|Activated_PI3K-delta_syndrome": 1,
    "not_specified|not_provided|Immunodeficiency_14|PIK3CD-related_disorder": 1,
    "not_specified|Immunodeficiency_14|PIK3CD-related_disorder": 1,
    "not_provided|Immunodeficiency_14|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14b|_autosomal_recessive": 1,
    "Activated_PI3K-delta_syndrome|Inborn_genetic_diseases|Immunodeficiency_14|not_provided": 1,
    "Combined_immunodeficiency_with_faciooculoskeletal_anomalies": 2,
    "Immunodeficiency_14|not_provided|Activated_PI3K-delta_syndrome": 1,
    "not_provided|Immunodeficiency_14|not_specified": 1,
    "not_provided|PIK3CD-related_disorder|Immunodeficiency_14": 1,
    "Immunodeficiency_14|not_provided|not_specified": 2,
    "Moyamoya_angiopathy": 29,
    "not_provided|Immunodeficiency_14b|_autosomal_recessive|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14|not_specified": 1,
    "Immunodeficiency_14|PIK3CD-related_disorder|not_specified": 1,
    "Activated_PI3K-delta_syndrome|PIK3CD-related_disorder|not_provided|Immunodeficiency_14": 1,
    "Immunodeficiency_14|not_provided|PIK3CD-related_disorder": 1,
    "Inborn_genetic_diseases|PIK3CD-related_disorder|Immunodeficiency_14": 1,
    "not_specified|not_provided|Immunodeficiency_14b|_autosomal_recessive|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14": 1,
    "PIK3CD-related_disorder|Immunodeficiency_14|not_specified|not_provided": 1,
    "not_specified|Immunodeficiency_14": 2,
    "not_provided|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive": 1,
    "Immunodeficiency_14b|_autosomal_recessive|Immunodeficiency_14|not_provided": 1,
    "Immunodeficiency_14|Immunodeficiency_14b|_autosomal_recessive|Combined_immunodeficiency_with_faciooculoskeletal_anomalies": 1,
    "not_specified|not_provided|Immunodeficiency_14": 1,
    "Immunodeficiency_14|not_specified|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14b|_autosomal_recessive": 1,
    "not_provided|Activated_PI3K-delta_syndrome|Immunodeficiency_14": 1,
    "Inherited_Immunodeficiency_Diseases|Inborn_genetic_diseases|Immunodeficiency_14|Combined_immunodeficiency_with_faciooculoskeletal_anomalies|Immunodeficiency_14b|_autosomal_recessive|not_provided": 1,
    "Leber_congenital_amaurosis_9": 147,
    "NMNAT1-related_disorder": 1,
    "Leber_congenital_amaurosis_9|Inborn_genetic_diseases": 5,
    "Retinal_dystrophy|Leber_congenital_amaurosis_9": 3,
    "Leber_congenital_amaurosis_9|Retinal_dystrophy|NMNAT1-related_disorder|not_provided": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_9": 1,
    "Leber_congenital_amaurosis_9|NMNAT1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_9": 5,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_9|Cone-rod_dystrophy": 1,
    "Leber_congenital_amaurosis_9|Spondyloepiphyseal_dysplasia|_sensorineural_hearing_loss|_impaired_intellectual_development|_and_leber_congenital_amaurosis": 3,
    "Cone_dystrophy|Leber_congenital_amaurosis_9": 1,
    "Retinal_dystrophy|Spondyloepiphyseal_dysplasia|_sensorineural_hearing_loss|_impaired_intellectual_development|_and_leber_congenital_amaurosis|Leber_congenital_amaurosis_9|not_provided": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_9": 3,
    "Spondyloepiphyseal_dysplasia|_sensorineural_hearing_loss|_impaired_intellectual_development|_and_leber_congenital_amaurosis": 1,
    "NMNAT1-related_retinopathy": 1,
    "Leber_congenital_amaurosis": 368,
    "not_provided|Leber_congenital_amaurosis_9|Spondyloepiphyseal_dysplasia|_sensorineural_hearing_loss|_impaired_intellectual_development|_and_leber_congenital_amaurosis|NMNAT1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|NMNAT1-related_disorder|Leber_congenital_amaurosis_9": 1,
    "Leber_congenital_amaurosis_9|not_provided": 2,
    "Leber_congenital_amaurosis_9|Retinal_dystrophy|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_9|Spondyloepiphyseal_dysplasia|_sensorineural_hearing_loss|_impaired_intellectual_development|_and_leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_9|Cone-rod_dystrophy": 1,
    "Leber_congenital_amaurosis_9|Inborn_genetic_diseases|Leber_congenital_amaurosis|Spondyloepiphyseal_dysplasia|_sensorineural_hearing_loss|_impaired_intellectual_development|_and_leber_congenital_amaurosis|Cone-rod_dystrophy|Retinal_dystrophy|not_provided|NMNAT1-related_disorder|Global_developmental_delay|Nystagmus|Severely_reduced_visual_acuity|Diarrhea|Developmental_regression|Gastrointestinal_dysmotility": 1,
    "Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma": 1,
    "not_provided|Neuroblastoma": 21,
    "Neuroblastoma": 110,
    "Pheochromocytoma|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2": 16,
    "not_specified|not_provided|KIF1B-related_disorder": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified": 4,
    "not_specified|Charcot-Marie-Tooth_disease_type_2": 300,
    "Charcot-Marie-Tooth_disease_type_2": 3832,
    "Charcot-Marie-Tooth_disease_type_2|not_specified": 450,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 25,
    "not_specified|Charcot-Marie-Tooth_disease_type_2A1": 5,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 12,
    "not_specified|KIF1B-related_disorder": 3,
    "Charcot-Marie-Tooth_disease|not_specified|KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 2,
    "Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|KIF1B-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 3,
    "Meniere_disease|not_provided|Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma|Neuroblastoma|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_specified|Neuroblastoma": 7,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified": 15,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|not_specified": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease": 4,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Charcot-Marie-Tooth_disease|Neuroblastoma": 1,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2A1": 7,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|Pheochromocytoma|not_specified": 1,
    "KIF1B-related_disorder|not_specified": 4,
    "not_specified|not_provided|Pheochromocytoma|Neuroblastoma|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "KIF1B-related_disorder|not_specified|Charcot-Marie-Tooth_disease_type_2": 3,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma|Pheochromocytoma": 1,
    "not_specified|not_provided|KIF1B-related_disorder|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma": 3,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 1,
    "Charcot-Marie-Tooth_disease|not_specified": 8,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 9,
    "Neuroblastoma|Charcot-Marie-Tooth_disease_type_2": 4,
    "Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma": 1,
    "KIF1B-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|KIF1B-related_disorder|not_specified": 1,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|not_specified": 6,
    "Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|KIF1B-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 42,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 49,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|_susceptibility_to|_1|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided": 16,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2A1|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2|not_specified": 3,
    "KIF1B-related_disorder": 23,
    "Pheochromocytoma": 188,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma|not_provided": 1,
    "KIF1B-related_disorder|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Pheochromocytoma|not_specified|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified": 13,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 3,
    "Neuroblastoma|not_specified": 1,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1": 8,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease|not_specified": 3,
    "Charcot-Marie-Tooth_disease|not_provided": 45,
    "not_provided|KIF1B-related_disorder": 5,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1": 3,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma": 2,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|not_specified|Charcot-Marie-Tooth_disease_type_2": 5,
    "Hereditary_cancer-predisposing_syndrome|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma": 4,
    "not_provided|Charcot-Marie-Tooth_disease_type_2": 170,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided": 196,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|KIF1B-related_disorder": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|KIF1B-related_disorder|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|KIF1B-related_disorder": 3,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2|KIF1B-related_disorder": 1,
    "Neuroblastoma|_susceptibility_to|_1": 4,
    "not_specified|Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified": 2,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Pheochromocytoma": 1,
    "Neuroblastoma|Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2A1|not_provided": 1,
    "not_specified|KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2": 2,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|KIF1B-related_disorder|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2A1|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|KIF1B-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2A1": 4,
    "not_provided|Charcot-Marie-Tooth_disease": 21,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 3,
    "KIF1B-related_disorder|not_provided": 4,
    "not_provided|Hemihypertrophy|Scoliosis|Decreased_muscle_mass|Congenital_contracture|Arthrogryposis_multiplex_congenita|Short_lower_limbs|Upper_limb_undergrowth": 1,
    "not_provided|Charcot-Marie-Tooth_disease|not_specified": 2,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 17,
    "not_provided|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "Neuroblastoma|_susceptibility_to|_1|KIF1B-related_disorder": 1,
    "KIF1B-related_disorder|not_specified|Malignant_tumor_of_breast|not_provided": 1,
    "Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 1,
    "Neuroblastoma|_susceptibility_to|_1|KIF1B-related_disorder|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4": 3796,
    "Charcot-Marie-Tooth_disease|_type_I": 609,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|Pheochromocytoma": 1,
    "not_specified|Charcot-Marie-Tooth_disease|not_provided|Hereditary_cancer|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "not_specified|Pheochromocytoma": 4,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma": 4,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Hereditary_cancer": 1,
    "Neuroblastoma|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "not_specified|Neuroblastoma|_susceptibility_to|_1": 1,
    "Charcot-Marie-Tooth_disease_type_2|KIF1B-related_disorder|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|Pain|Joint_laxity|EMG_abnormality|EMG:_myopathic_abnormalities|not_specified|Pheochromocytoma": 1,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|KIF1B-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma|Malignant_tumor_of_breast": 1,
    "Multiple_endocrine_neoplasia_type_2A|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|not_provided": 1,
    "Adrenal_pheochromocytoma|Palpitations|Recurrent_paroxysmal_headache": 1,
    "not_provided|KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma": 1,
    "not_specified|Pheochromocytoma|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuroblastoma|not_provided|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|not_provided|Neuroblastoma|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified": 4,
    "Global_developmental_delay|Exaggerated_startle_response|EEG_abnormality|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "Hereditary_cancer-predisposing_syndrome": 55043,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|not_specified": 3,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 1,
    "not_specified|Charcot-Marie-Tooth_disease": 9,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|not_provided": 1,
    "Pheochromocytoma|not_specified": 3,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease|Hereditary_cancer-predisposing_syndrome|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Charcot-Marie-Tooth_disease|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma": 1,
    "Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Neuroblastoma|KIF1B-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_cancer-predisposing_syndrome|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Neuroblastoma": 2,
    "Charcot-Marie-Tooth_disease_type_2A1|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Neuroblastoma": 2,
    "Ovarian_cancer": 164,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|_susceptibility_to|_1|Neuroblastoma|not_specified": 1,
    "not_specified|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|not_specified": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Neuroblastoma": 1,
    "not_provided|Neuroblastoma|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Neuroblastoma|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2": 1,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|not_specified|Charcot-Marie-Tooth_disease_type_2": 3,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|Charcot-Marie-Tooth_disease": 1,
    "Meniere_disease": 73,
    "KIF1B-related_disorder|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2": 8,
    "Charcot-Marie-Tooth_disease|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma|Neuroblastoma|_susceptibility_to|_1": 1,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|not_specified|Charcot-Marie-Tooth_disease_type_2|Neuroblastoma": 1,
    "not_specified|Neuroblastoma|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|KIF1B-related_disorder|not_provided|not_specified": 1,
    "not_specified|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1": 2,
    "not_specified|EMG_abnormality|EMG:_axonal_abnormality|Distal_muscle_weakness|Vitiligo|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|NEUROBLASTOMA|_SUSCEPTIBILITY_TO|_1|_INCLUDED|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Pheochromocytoma": 2,
    "not_specified|Neuroblastoma|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|not_specified|KIF1B-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1": 1,
    "Charcot-Marie-Tooth_disease|Pheochromocytoma|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Neuroblastoma|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|not_specified|KIF1B-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_cancer-predisposing_syndrome|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Neuroblastoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Meniere_disease|not_specified": 1,
    "Neuroblastoma|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Neuroblastoma|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A1|Neuroblastoma|_susceptibility_to|_1|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Pheochromocytoma|Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Neuroblastoma|_susceptibility_to|_1|Charcot-Marie-Tooth_disease_type_2A1|Ovarian_cancer|not_specified": 1,
    "Pheochromocytoma|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2A1|Pheochromocytoma": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma|KIF1B-related_disorder": 1,
    "not_specified|Pheochromocytoma|Charcot-Marie-Tooth_disease|not_provided|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A1": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Neuroblastoma|_susceptibility_to|_1": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Gait_ataxia": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuroblastoma|not_specified|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|KIF1B-related_disorder|not_provided|Neuroblastoma": 1,
    "Neuroblastoma|Pheochromocytoma|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Pheochromocytoma|not_provided|Neuroblastoma|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuroblastoma|Pheochromocytoma|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuroblastoma|not_provided": 3,
    "Neuroblastoma|Charcot-Marie-Tooth_disease_type_2|Pheochromocytoma|not_provided": 1,
    "PEX14-related_disorder": 7,
    "not_provided|PEX14-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K": 316,
    "PEX14-related_disorder|Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases|not_provided": 1,
    "PEX14-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K|PEX14-related_disorder": 2,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|PEX14-related_disorder": 5,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases": 15,
    "not_specified|Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_specified": 2,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)|PEX14-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided": 19,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K": 10,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K": 9,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_specified|not_provided": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)": 13,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 5,
    "PEX14-related_disorder|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified|Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_provided": 1,
    "PEX14-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_K": 4,
    "PEX14-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided": 2,
    "not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases|PEX14-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|PEX14-related_disorder|not_provided": 3,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified": 1,
    "not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K": 1,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K|PEX14-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|PEX14-related_disorder|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_provided": 2,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)": 40,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|_complementation_group_K": 4,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|PEX14-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided": 1,
    "PEX14-related_disorder|Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|PEX14-related_disorder": 1,
    "not_specified|Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified|not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|PEX14-related_disorder": 3,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|not_specified": 1,
    "not_specified|Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K": 1,
    "Peroxisome_biogenesis_disorder|_complementation_group_K|PEX14-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "not_specified|Peroxisome_biogenesis_disorder|_complementation_group_K|not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "PEX14-related_disorder|not_provided|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K|Peroxisome_biogenesis_disorder_13A_(Zellweger)|not_specified": 1,
    "not_provided|Peroxisome_biogenesis_disorder|_complementation_group_K|not_specified|Peroxisome_biogenesis_disorder_13A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_13A_(Zellweger)|Peroxisome_biogenesis_disorder|_complementation_group_K|Inborn_genetic_diseases": 1,
    "not_specified|Peroxisome_biogenesis_disorder_13A_(Zellweger)|PEX14-related_disorder": 1,
    "Neutrophil_inclusion_bodies|not_provided": 1,
    "CASZ1-related_disorder|not_provided": 5,
    "CASZ1-related_disorder": 4,
    "not_provided|CASZ1-related_disorder": 2,
    "CASZ1-related_dilated_cardiomyopathy": 1,
    "CASZ1-associated_cardiomyopathy": 1,
    "not_specified|CASZ1-related_disorder": 1,
    "Heterotaxy|_visceral|_14|_autosomal": 3,
    "See_cases|not_specified|not_provided": 3,
    "Amyotrophic_lateral_sclerosis_type_10": 60,
    "not_provided|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 4,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|Frontotemporal_dementia": 3,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 41,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Inborn_genetic_diseases": 3,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|Inborn_genetic_diseases": 3,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10": 38,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Inborn_genetic_diseases|not_provided": 4,
    "TARDBP-related_disorder": 4,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 4,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|not_provided": 2,
    "TARDBP-related_disorder|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|Inborn_genetic_diseases|not_provided|Parkinsonian_disorder": 1,
    "TARDBP-related_disorder|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 2,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|TARDBP-related_disorder": 2,
    "Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|TARDBP-related_disorder|not_provided": 1,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|not_specified": 2,
    "Inborn_genetic_diseases|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10": 4,
    "TARDBP-related_disorder|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_10|not_provided|Inborn_genetic_diseases|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 1,
    "Amyotrophic_lateral_sclerosis_type_10|not_provided|not_specified": 1,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|not_provided": 5,
    "FRONTOTEMPORAL_DEMENTIA_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 1,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|TARDBP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Motor_neuron_disease|TARDBP-related_disorder|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|not_provided": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_10": 1,
    "Amyotrophic_lateral_sclerosis_type_10|not_provided|TARDBP-related_disorder|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 2,
    "not_provided|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10": 2,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|TARDBP-related_disorder|not_provided": 2,
    "Motor_neuron_disease": 12,
    "Inborn_genetic_diseases|Amyotrophic_Lateral_Sclerosis|_Dominant|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|not_specified|not_provided|Frontotemporal_dementia": 1,
    "TARDBP-related_disorder|Amyotrophic_lateral_sclerosis_type_10": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Inborn_genetic_diseases": 1,
    "Motor_neuron_disease|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 1,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|TARDBP-related_disorder": 1,
    "Frontotemporal_dementia": 181,
    "FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|TARDBP-related_disorder|not_provided|FRONTOTEMPORAL_DEMENTIA_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_10|TARDBP-related_disorder|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|See_cases": 1,
    "not_provided|TARDBP-related_disorder|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10": 1,
    "Amyotrophic_lateral_sclerosis_type_10|TARDBP-related_disorder": 1,
    "Inborn_genetic_diseases|TARDBP-related_disorder": 1,
    "Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant|not_provided|Amyotrophic_lateral_sclerosis_type_10": 1,
    "Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant": 3,
    "FRONTOTEMPORAL_DEMENTIA_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED|Amyotrophic_lateral_sclerosis_type_10|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_TDP43_INCLUSIONS|_TARDBP-RELATED": 1,
    "Amyotrophic_lateral_sclerosis_type_10|Immunodeficiency_due_to_MASP-2_deficiency": 1,
    "Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant|Immunodeficiency_due_to_MASP-2_deficiency": 1,
    "Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant|Immunodeficiency_due_to_MASP-2_deficiency|Amyotrophic_lateral_sclerosis_type_10": 1,
    "Immunodeficiency_due_to_MASP-2_deficiency": 49,
    "Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant|not_provided|Immunodeficiency_due_to_MASP-2_deficiency": 1,
    "Immunodeficiency_due_to_MASP-2_deficiency|Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "not_specified|MASP2-related_disorder": 3,
    "MASP2-related_disorder": 8,
    "MASP2-related_disorder|not_specified": 1,
    "not_provided|MASP2-related_disorder": 2,
    "not_provided|Immunodeficiency_due_to_MASP-2_deficiency": 17,
    "not_specified|Immunodeficiency_due_to_MASP-2_deficiency": 4,
    "Frontotemporal_dementia|not_provided|Immunodeficiency_due_to_MASP-2_deficiency|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Immunodeficiency_due_to_MASP-2_deficiency|not_specified": 3,
    "not_specified|not_provided|Frontotemporal_dementia|Amyotrophic_Lateral_Sclerosis|_Dominant|Immunodeficiency_due_to_MASP-2_deficiency": 1,
    "not_provided|Immunodeficiency_due_to_MASP-2_deficiency|not_specified": 1,
    "not_provided|Immunodeficiency_due_to_MASP-2_deficiency|MASP2-related_disorder": 1,
    "not_specified|not_provided|Immunodeficiency_due_to_MASP-2_deficiency": 1,
    "MASP2-related_disorder|Immunodeficiency_due_to_MASP-2_deficiency": 2,
    "Immunodeficiency_due_to_MASP-2_deficiency|not_provided": 3,
    "MASP2-related_disorder|not_provided": 1,
    "MASP2-related_disorder|not_specified|Immunodeficiency_due_to_MASP-2_deficiency|not_provided": 1,
    "not_provided|MASP2-related_disorder|Immunodeficiency_due_to_MASP-2_deficiency": 1,
    "not_provided|MTOR-related_disorder": 39,
    "Autosomal_dominant_epilepsy|not_provided": 1,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 39,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided": 17,
    "not_provided|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 10,
    "CEBALID_syndrome": 26,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes": 12,
    "MTOR-related_disorder|not_provided": 22,
    "MTOR-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|CEBALID_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II": 62,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|CEBALID_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "CEBALID_syndrome|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|Inborn_genetic_diseases": 1,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided|Macrocephaly": 1,
    "MTOR-related_disorder": 21,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "not_specified|not_provided|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 1,
    "Neurodevelopmental_disorder|_MTOR_related|Inborn_genetic_diseases|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided": 4,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_provided": 4,
    "Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 4,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Isolated_focal_cortical_dysplasia_type_II": 3,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II": 5,
    "not_provided|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes": 5,
    "CEBALID_syndrome|Isolated_focal_cortical_dysplasia_type_II|MTOR-related_megalencephaly_and_pigmentary_mosaicism_in_skin|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|MTOR-related_disorder|not_provided": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_provided|Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 1,
    "Overgrowth_syndrome|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_specified|MTOR-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided": 2,
    "not_provided|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_specified|not_provided|MTOR-related_disorder|Inborn_genetic_diseases": 1,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|CEBALID_syndrome|Isolated_focal_cortical_dysplasia_type_II|Rare_genetic_intellectual_disability|Inborn_genetic_diseases|not_provided|Intellectual_disability|Intellectual_disability|_severe": 1,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Abnormal_facial_shape|Abnormality_of_the_skeletal_system|Macrocephaly|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|MTOR-related_disorder": 1,
    "not_provided|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|Inborn_genetic_diseases|MTOR-related_disorder": 1,
    "not_provided|not_specified|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 1,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided|CEBALID_syndrome|Intellectual_disability": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided": 4,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_provided|CEBALID_syndrome|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 1,
    "Hemimegalencephaly|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes": 1,
    "Inborn_genetic_diseases|MTOR-related_disorder|not_provided": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome": 2,
    "Intellectual_disability|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder|_MTOR_related": 1,
    "not_specified|Isolated_focal_cortical_dysplasia_type_II|Inborn_genetic_diseases|not_provided": 1,
    "Seizure|not_provided": 7,
    "Inborn_genetic_diseases|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "not_provided|Papillary_renal_cell_carcinoma_type_1": 9,
    "Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_provided|MTOR-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_specified|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|MTOR-related_disorder": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|not_provided": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Macrocephaly-intellectual_disability-neurodevelopmental_disorder-small_thorax_syndrome|Inborn_genetic_diseases|not_provided|MTOR-related_disorder": 1,
    "Autism_spectrum_disorder|not_provided": 21,
    "not_provided|not_specified|MTOR-related_disorder": 1,
    "not_provided|not_specified|Papillary_renal_cell_carcinoma_type_1": 1,
    "Overgrowth_syndrome": 3,
    "not_provided|MTOR-related_disorder|not_specified": 1,
    "Schnyder_crystalline_corneal_dystrophy": 83,
    "Schnyder_crystalline_corneal_dystrophy|not_provided": 1,
    "Schnyder_crystalline_corneal_dystrophy|not_specified": 2,
    "not_provided|Schnyder_crystalline_corneal_dystrophy": 11,
    "not_specified|Schnyder_crystalline_corneal_dystrophy": 2,
    "not_provided|Schnyder_crystalline_corneal_dystrophy|UBIAD1-related_disorder": 1,
    "UBIAD1-related_disorder": 2,
    "DISP3-related_disorder": 32,
    "DISP3-related_disorder|not_provided": 2,
    "FBXO2-related_disorder": 6,
    "not_provided|MAD2L2-related_disorder": 5,
    "MAD2L2-related_disorder|not_provided": 5,
    "MAD2L2-related_disorder": 2,
    "Fanconi_anemia_complementation_group_V|not_provided": 1,
    "MAD2L2-related_disorder|not_provided|not_specified": 1,
    "Oligospermia|Reduced_sperm_motility|Abnormal_sperm_morphology": 12,
    "Neural_tube_defects|_folate-sensitive": 70,
    "not_provided|Neural_tube_defects|_folate-sensitive": 3,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided": 11,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 17,
    "Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Intellectual_disability": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 600,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive": 11,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Schizophrenia|Neural_tube_defects|_folate-sensitive|Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|MTHFR-related_disorder|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Inborn_genetic_diseases|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 16,
    "Inborn_genetic_diseases|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|MTHFR-related_disorder": 9,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Inborn_genetic_diseases": 19,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified|MTHFR-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided": 1,
    "Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 17,
    "not_provided|Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 4,
    "Prostate_cancer": 597,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive|Schizophrenia": 2,
    "MTHFR-related_disorder|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Rare_genetic_intellectual_disability|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive": 1,
    "Schizophrenia|Thrombophilia_due_to_thrombin_defect|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|not_provided": 2,
    "Neural_tube_defect|Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive|Schizophrenia": 2,
    "MTHFR-related_disorder|not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Neural_tube_defects|_folate-sensitive|not_provided|Thrombophilia_due_to_thrombin_defect|Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Spasticity|Bilateral_tonic-clonic_seizure|Global_developmental_delay|Infantile_spasms|Secondary_microcephaly": 1,
    "MTHFR-related_disorder|Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Schizophrenia|not_provided": 1,
    "Intellectual_disability|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|MTHFR-related_disorder|Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided|See_cases": 1,
    "Thrombophilia_due_to_thrombin_defect": 3,
    "Global_developmental_delay|Lower_limb_spasticity|Bilateral_tonic-clonic_seizure|Mental_deterioration|Delayed_speech_and_language_development|not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Schizophrenia|Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 3,
    "not_specified|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Schizophrenia|Thrombophilia_due_to_thrombin_defect": 5,
    "MTHFR-related_disorder|Schizophrenia|Thrombophilia_due_to_thrombin_defect|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|not_provided": 1,
    "Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided": 4,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect|MTHFR-related_disorder|not_provided": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|MTHFR-related_disorder|not_provided": 2,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases": 1,
    "not_specified|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 3,
    "not_specified|MTHFR-related_disorder": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Thrombophilia_due_to_thrombin_defect|Schizophrenia|not_provided": 2,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified|not_provided": 2,
    "Neural_tube_defects|_folate-sensitive|MTHFR-related_disorder": 1,
    "MTHFR-related_disorder|Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive|Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified|not_provided|Gastrointestinal_stromal_tumor|MTHFR_THERMOLABILE_POLYMORPHISM|Schizophrenia|_susceptibility_to": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|MTHFR-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive": 2,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided|not_specified": 2,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified": 3,
    "Mendelian_syndromes_with_cleft_lip/palate|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|not_provided": 1,
    "not_provided|Neural_tube_defects|_folate-sensitive|Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Thrombophilia_due_to_thrombin_defect": 1,
    "See_cases|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|MTHFR-related_disorder": 2,
    "Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive|Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified": 1,
    "Thrombophilia_due_to_thrombin_defect|Intellectual_disability|Neural_tube_defects|_folate-sensitive|Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Vascular_dementia": 21,
    "Mendelian_syndromes_with_cleft_lip/palate": 7,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Thrombophilia_due_to_thrombin_defect|Schizophrenia": 1,
    "Autism|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "MTHFR-related_disorder": 6,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified": 5,
    "Inborn_genetic_diseases|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|MTHFR-related_disorder": 1,
    "Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Thrombophilia_due_to_thrombin_defect|Neural_tube_defects|_folate-sensitive": 1,
    "not_provided|Inborn_genetic_diseases|MTHFR-related_disorder|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "Thrombophilia_due_to_thrombin_defect|methotrexate_response_-_Toxicity|not_specified|not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Gastrointestinal_stromal_tumor|Neural_tube_defects|_folate-sensitive|MTHFR_THERMOLABILE_POLYMORPHISM|See_cases": 1,
    "Generalized_cerebral_atrophy/hypoplasia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Abnormality_of_metabolism/homeostasis": 1,
    "Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Schizophrenia|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect": 2,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Neural_tube_defects|_folate-sensitive|not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "MTHFR-related_disorder|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided|not_specified": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Neural_tube_defects|_folate-sensitive|Schizophrenia|Thrombophilia_due_to_thrombin_defect": 2,
    "Neural_tube_defects|_folate-sensitive|Schizophrenia|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Thrombophilia_due_to_thrombin_defect": 1,
    "not_provided|Neural_tube_defects|_folate-sensitive|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|Thrombophilia_due_to_thrombin_defect|Schizophrenia": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided|Thrombophilia_due_to_thrombin_defect|Schizophrenia|Neural_tube_defects|_folate-sensitive": 1,
    "Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Neurodegeneration|_childhood-onset|_with_hypotonia|_respiratory_insufficiency|_and_brain_imaging_abnormalities": 10,
    "CLCN6-related_disorder": 4,
    "not_provided|Neurodegeneration|_childhood-onset|_with_hypotonia|_respiratory_insufficiency|_and_brain_imaging_abnormalities": 4,
    "Neurodegeneration|_childhood-onset|_with_hypotonia|_respiratory_insufficiency|_and_brain_imaging_abnormalities|not_provided": 2,
    "CLCN6-related_disorder|not_provided": 1,
    "not_provided|CLCN6-related_disorder": 2,
    "Global_developmental_delay|Movement_disorder|Abnormality_of_temperature_regulation|EEG_abnormality|Neurogenic_bladder|Abnormality_of_the_respiratory_system|Abnormal_speech_pattern|Abnormality_of_vision|Abnormality_of_the_skin|Motor_delay|Feeding_difficulties|Hypotonia|Neurodegeneration|_childhood-onset|_with_hypotonia|_respiratory_insufficiency|_and_brain_imaging_abnormalities": 1,
    "not_provided|not_specified|See_cases": 4,
    "Atrial_fibrillation|_familial|_6": 122,
    "not_specified|Atrial_fibrillation|_familial|_6|not_provided": 1,
    "Atrial_standstill_2|not_specified|Atrial_fibrillation|_familial|_6": 1,
    "Atrial_fibrillation|_familial|_6|not_provided": 3,
    "Atrial_fibrillation|_familial|_6|not_specified": 1,
    "Vascular_dementia|not_provided|Atrial_fibrillation|_familial|_6": 1,
    "Atrial_standstill_2|Atrial_fibrillation|_familial|_6|not_provided": 1,
    "Inborn_genetic_diseases|Atrial_fibrillation|_familial|_6": 3,
    "Atrial_fibrillation|_familial|_6|not_specified|not_provided": 1,
    "Atrial_fibrillation|_familial|_6|Atrial_standstill_2": 2,
    "not_specified|Atrial_fibrillation|_familial|_6": 2,
    "Atrial_fibrillation|_familial|_6|Inborn_genetic_diseases": 4,
    "not_provided|Atrial_fibrillation|_familial|_6": 3,
    "not_specified|Atrial_fibrillation|_familial|_6|Inborn_genetic_diseases|Atrial_standstill_2": 1,
    "NPPA-related_disorder|not_specified|Atrial_fibrillation|_familial|_6|not_provided|Atrial_standstill_2": 1,
    "NPPA-related_disorder|Atrial_fibrillation|_familial|_6": 1,
    "Cardiac_arrhythmia|not_specified|not_provided|Atrial_fibrillation|_familial|_6": 1,
    "Atrial_fibrillation|_familial|_6|NPPA-related_disorder": 1,
    "NPPA-related_disorder": 1,
    "Atrial_fibrillation|_familial|_6|Atrial_standstill_2|not_specified": 1,
    "RNU5E-1-associated_neurodevelopmental_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided": 12,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 557,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 87,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 98,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 5,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome": 123,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 24,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 6,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|not_provided": 1,
    "PLOD1-related_disorder": 4,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|PLOD1-related_disorder|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 8,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Keratoconus|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "PLOD1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 9,
    "PLOD1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 15,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided": 8,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 12,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Ehlers-Danlos_syndrome": 2,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 10,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided": 2,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "PLOD1-related_disorder|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided": 3,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 7,
    "not_provided|Ehlers-Danlos_syndrome": 14,
    "Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 1,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|PLOD1-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 2,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|PLOD1-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|PLOD1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|not_specified": 2,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 5,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|PLOD1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|not_provided": 3,
    "PLOD1-related_disorder|not_provided|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PLOD1-related_disorder|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|PLOD1-related_disorder|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Ehlers-Danlos_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 2,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|PLOD1-related_disorder": 1,
    "PLOD1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|PLOD1-related_disorder": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified": 2,
    "PLOD1-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 2,
    "Hypoplasia_of_scrotum|Bilateral_cryptorchidism|Short_chin|Feeding_difficulties|Joint_hypermobility|Generalized_neonatal_hypotonia|Thoracolumbar_scoliosis|Generalized_hypotonia|Congenital_omphalocele|Depressed_nasal_bridge|High_palate|Porencephalic_cyst|Macrocephaly_at_birth|Narrow_chest|Dolichocephaly|Hydrocephalus|Neonatal_hypotonia|Severe_global_developmental_delay|Umbilical_hernia": 1,
    "Cardiovascular_phenotype": 29700,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PLOD1-related_disorder": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "PLOD1-related_disorder|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided": 1,
    "Myopathy": 26,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_specified|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 33,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2": 19,
    "not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_provided|Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy|not_provided": 1,
    "not_specified|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2": 2,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2": 9,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 75,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Optic_atrophy": 1,
    "Inborn_genetic_diseases|MFN2-related_disorder|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_provided": 12,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 8,
    "not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 18,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 15,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_specified": 3,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Optic_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "MFN2-related_disorder|Charcot-Marie-Tooth_disease_type_2": 5,
    "MFN2-related_disorder|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2": 23,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 9,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2": 4,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided": 4,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2": 7,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2A2|Microcephaly|Distal_muscle_weakness|Abnormality_of_the_dentition|Decreased_body_weight|EMG_abnormality|Abnormal_dental_enamel_morphology|Nail_dystrophy|Scarring|Abnormal_blistering_of_the_skin|Alopecia_of_scalp|Failure_to_thrive|Short_stature|Hyperpigmentation_of_the_skin|Scarring_alopecia_of_scalp": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2A2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 99,
    "Cerebellar_ataxia|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease_type_2": 9,
    "Peripheral_neuropathy|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 6,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A": 2,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease|MFN2-related_disorder": 1,
    "MFN2-related_disorder": 6,
    "Hereditary_motor_neuron_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "MFN2-related_disorder|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2": 1,
    "Retinal_dystrophy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Tip-toe_gait": 40,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2A2": 2,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 3,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2|Distal_lower_limb_amyotrophy|Peripheral_axonal_neuropathy|Distal_muscle_weakness": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 3,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 4,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 3,
    "Charcot-Marie-Tooth_disease_type_2A2|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease": 4,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Multiple_symmetric_lipomatosis|Charcot-Marie-Tooth_disease_type_2A2|MFN2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2A2": 2,
    "Auditory_neuropathy": 41,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2A2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|_type_2A": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 3,
    "Charcot-Marie-Tooth_disease_type_2A2|not_provided|Inborn_genetic_diseases|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Multiple_system_atrophy|_cerebellar_type|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Optic_atrophy": 1,
    "MFN2-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Inborn_genetic_diseases|MFN2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_provided|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Retinal_dystrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_specified|not_provided": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Severe_early-onset_axonal_neuropathy_due_to_MFN2_deficiency": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2A2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|not_specified|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 3,
    "Global_developmental_delay|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2A2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|MFN2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease": 3,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 6,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 3,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2": 5,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A1|Charcot-Marie-Tooth_disease|_type_2A|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Peripheral_neuropathy": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2|not_specified|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease": 1,
    "Optic_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Retinal_dystrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2A2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 2,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_ataxia|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|MFN2-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Multiple_symmetric_lipomatosis|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease_type_2A2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_specified": 7,
    "MFN2-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Peripheral_neuropathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease|MFN2-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_motor_and_sensory_neuropathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_specified|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_2": 2,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2": 10,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2A2|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease|_type_2A|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Multiple_symmetric_lipomatosis|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Neuropathy|_hereditary_motor_and_sensory|_type_6A|MFN2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Tip-toe_gait|Peripheral_axonal_neuropathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|MFN2-related_disorder|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "MFN2-related_disorder|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B": 1,
    "Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|MFN2-related_disorder|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|not_specified": 1,
    "Cerebral_palsy": 16,
    "Multiple_symmetric_lipomatosis|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|Neuropathy|_hereditary_motor_and_sensory|_type_6A|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Neuropathy|_hereditary_motor_and_sensory|_type_6A": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease|_axonal|_autosomal_recessive|_type_2a2b%3B|Charcot-Marie-Tooth_disease_type_2A2|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_motor_and_sensory_neuropathy|Charcot-Marie-Tooth_disease_type_2": 6,
    "not_provided|Hereditary_motor_and_sensory_neuropathy_with_optic_atrophy|Charcot-Marie-Tooth_disease_type_2": 5,
    "Hereditary_motor_and_sensory_neuropathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_motor_and_sensory_neuropathy": 1,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_plasma_levels_of_TNF|_TNFR|_and/or_TNFR2|Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Associated_with_severe_COVID-19_disease": 1,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_plasma_levels_of_TNF|_TNFR|_and/or_TNFR3|Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Associated_with_severe_COVID-19_disease": 1,
    "VPS13D-related_disorder": 7,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome": 41,
    "VPS13D-related_disorder|not_provided": 42,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|VPS13D-related_disorder": 1,
    "Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|VPS13D-related_disorder|not_provided": 1,
    "not_provided|VPS13D-related_disorder": 18,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|not_provided": 3,
    "not_provided|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|VPS13D-related_disorder": 2,
    "Inborn_genetic_diseases|VPS13D-related_disorder": 1,
    "not_provided|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome": 6,
    "Non-immune_hydrops_fetalis": 24,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|VPS13D-related_disorder|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome": 1,
    "not_provided|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|VPS13D-related_disorder": 1,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|Inborn_genetic_diseases|not_provided|VPS13D-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome": 2,
    "VPS13D-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "VPS13D-related_disorder|not_provided|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome": 1,
    "Leigh_syndrome": 2125,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome": 3,
    "Autosomal_recessive_cerebellar_ataxia": 10,
    "Spinocerebellar_atrophy": 1,
    "not_provided|VPS13D-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|VPS13D-related_disorder": 1,
    "Autosomal_recessive_cerebellar_ataxia-saccadic_intrusion_syndrome|Spinocerebellar_ataxia_type_4": 1,
    "DHRS3_Deficiency": 3,
    "DHRS3-related_disorder": 5,
    "Mayer-Rokitansky-Kuster-Hauser_syndrome": 1,
    "Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 22,
    "Low_bone_mineral_density": 1,
    "Flexion_contracture": 23,
    "not_provided|CTRC-related_disorder|Hereditary_pancreatitis": 2,
    "Hereditary_pancreatitis": 2111,
    "Hereditary_pancreatitis|not_provided": 156,
    "not_provided|Hereditary_pancreatitis": 178,
    "CTRC-related_disorder": 2,
    "Hereditary_pancreatitis|Pancreatitis|_chronic|_susceptibility_to": 1,
    "Hereditary_pancreatitis|not_specified|not_provided": 5,
    "not_provided|Hereditary_pancreatitis|not_specified": 6,
    "Hereditary_pancreatitis|CTRC-related_disorder": 3,
    "not_specified|not_provided|Hereditary_pancreatitis": 7,
    "not_specified|Hereditary_pancreatitis": 38,
    "Hereditary_pancreatitis|not_specified": 40,
    "CTRC-related_disorder|Hereditary_pancreatitis": 1,
    "not_specified|CTRC-related_disorder|Hereditary_pancreatitis": 1,
    "Chronic_pancreatitis": 1,
    "not_specified|not_provided|Hereditary_pancreatitis|Pancreatitis|_chronic|_susceptibility_to": 1,
    "not_provided|not_specified|Hereditary_pancreatitis|Pancreatitis|_chronic|_susceptibility_to": 1,
    "CELA2A-related_disorder|Abdominal_obesity-metabolic_syndrome_4|Coronary_artery_disorder|Hypertriglyceridemia|Diabetes|Hypertensive_disorder": 1,
    "Coronary_artery_disorder|Diabetes|Hypertensive_disorder|Hypertriglyceridemia|Abdominal_obesity-metabolic_syndrome_4": 3,
    "Abdominal_obesity-metabolic_syndrome_4": 4,
    "CASP9-related_disorder": 12,
    "CASP9-related_disorder|not_provided": 4,
    "not_provided|CASP9-related_disorder": 2,
    "Dilated_Cardiomyopathy|_Recessive": 661,
    "Dilated_Cardiomyopathy|_Recessive|not_specified": 49,
    "not_provided|Dilated_Cardiomyopathy|_Recessive": 14,
    "Dilated_Cardiomyopathy|_Recessive|not_provided": 11,
    "Dilated_Cardiomyopathy|_Recessive|PLEKHM2-related_disorder|not_provided": 1,
    "not_specified|Dilated_Cardiomyopathy|_Recessive": 40,
    "not_specified|PLEKHM2-related_disorder|Dilated_Cardiomyopathy|_Recessive": 1,
    "not_provided|Dilated_Cardiomyopathy|_Recessive|not_specified": 2,
    "PLEKHM2-related_disorder|Dilated_Cardiomyopathy|_Recessive": 2,
    "not_provided|Dilated_Cardiomyopathy|_Recessive|PLEKHM2-related_disorder": 2,
    "PLEKHM2-related_disorder|Dilated_Cardiomyopathy|_Recessive|not_specified": 2,
    "SPEN-related_disorder": 75,
    "Radio-Tartaglia_syndrome": 78,
    "Radio-Tartaglia_syndrome|Developmental_disorder": 1,
    "SPEN-related_disorder|not_provided": 21,
    "Radio-Tartaglia_syndrome|not_provided": 9,
    "SPEN-related_disorder|Inborn_genetic_diseases": 4,
    "SPEN-related_disorder|Radio-Tartaglia_syndrome": 1,
    "Inborn_genetic_diseases|SPEN-related_disorder": 5,
    "Radio-Tartaglia_syndrome|Inborn_genetic_diseases": 4,
    "not_provided|Neurodevelopmental_abnormality|Inborn_genetic_diseases|Radio-Tartaglia_syndrome": 1,
    "not_provided|SPEN-related_disorder": 9,
    "not_provided|SPEN-related_disorder|Radio-Tartaglia_syndrome": 1,
    "Myoepithelial_tumor": 83,
    "SPEN-related_disorder|Radio-Tartaglia_syndrome|not_provided": 2,
    "SPEN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Encephalopathy|Radio-Tartaglia_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Radio-Tartaglia_syndrome": 3,
    "Inborn_genetic_diseases|Radio-Tartaglia_syndrome|not_provided": 1,
    "Breast_ductal_adenocarcinoma": 33,
    "not_provided|Autism_spectrum_disorder": 33,
    "SPEN-related_neurodevelopmental_disorder": 1,
    "not_specified|SPEN-related_disorder|not_provided": 1,
    "SPEN-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|SPEN-related_disorder|not_provided": 1,
    "not_provided|Radio-Tartaglia_syndrome": 1,
    "Inborn_genetic_diseases|SPEN-related_disorder|Radio-Tartaglia_syndrome|not_provided": 1,
    "ZBTB17-related_disorder": 8,
    "Primary_dilated_cardiomyopathy|not_provided": 35,
    "Spinocerebellar_ataxia_type_1": 8,
    "Oromandibular-limb_hypogenesis_spectrum": 20,
    "Bartter_disease_type_4B": 7,
    "Sensorineural_hearing_loss_disorder|Bartter_disease_type_3|Bartter_disease_type_4B": 1,
    "Bartter_disease_type_4B|not_specified|not_provided": 1,
    "Bartter_disease_type_4B|not_provided": 8,
    "not_provided|Bartter_disease_type_4B": 4,
    "Bartter_disease_type_4B|Inborn_genetic_diseases": 2,
    "Bartter_syndrome_type_4": 2,
    "not_specified|Bartter_disease_type_4B|not_provided": 1,
    "CHARGE_syndrome|Bartter_disease_type_4B|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|Deafness": 22,
    "not_provided|Bartter_disease_type_3|Bartter_disease_type_4B": 27,
    "Bartter_disease_type_3|Bartter_disease_type_4B": 78,
    "Bartter_disease_type_3": 19,
    "Bartter_disease_type_4B|Bartter_disease_type_3|not_provided": 18,
    "Bartter_disease_type_3|Bartter_disease_type_4B|not_provided": 25,
    "Inborn_genetic_diseases|Bartter_disease_type_3|Bartter_disease_type_4B": 5,
    "not_provided|Bartter_disease_type_4B|not_specified|Bartter_disease_type_3": 1,
    "Bartter_disease_type_3|Bartter_disease_type_4B|not_provided|Inborn_genetic_diseases": 3,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Bartter_disease_type_3|Bartter_disease_type_4B|not_provided": 1,
    "Bartter_syndrome|_type_3|_with_hypocalciuria": 1,
    "not_provided|Bartter_disease_type_4B|Bartter_disease_type_3": 9,
    "Bartter_disease_type_3|Bartter_disease_type_4B|not_specified|not_provided": 1,
    "Bartter_disease_type_4B|Bartter_disease_type_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Bartter_disease_type_3": 3,
    "Bartter_syndrome": 31,
    "not_specified|not_provided|Bartter_disease_type_3|Bartter_disease_type_4B": 3,
    "not_provided|not_specified|Bartter_disease_type_4B|Bartter_disease_type_3": 3,
    "not_specified|not_provided|Bartter_disease_type_3|Hematuria|Proteinuria": 1,
    "not_specified|not_provided|Bartter_disease_type_4B|Bartter_disease_type_3": 2,
    "not_provided|Autosomal_dominant_osteopetrosis_1|Bartter_disease_type_3|Bartter_disease_type_4B": 1,
    "not_provided|Bartter_disease_type_3|Hematuria|Proteinuria": 1,
    "Inborn_genetic_diseases|Bartter_disease_type_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_3|Bartter_disease_type_4B": 2,
    "Bartter_disease_type_3|not_provided|Bartter_disease_type_4B": 1,
    "Bartter_syndrome|Bartter_disease_type_3|Bartter_disease_type_4B|not_provided": 1,
    "not_provided|Bartter_syndrome|Bartter_disease_type_3|Bartter_disease_type_4B": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_4B|Bartter_disease_type_3|not_specified": 1,
    "Inborn_genetic_diseases|Bartter_disease_type_4B|Bartter_disease_type_3": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_4B|Bartter_disease_type_3": 3,
    "Inborn_genetic_diseases|Bartter_disease_type_3|Bartter_disease_type_4B|not_provided": 2,
    "Bartter_disease_type_3|Bartter_disease_type_4B|Inborn_genetic_diseases": 2,
    "Bartter_disease_type_4B|Bartter_disease_type_3|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Bartter_disease_type_4B|Bartter_disease_type_3": 1,
    "not_specified|Bartter_disease_type_3|Bartter_disease_type_4B|not_provided": 2,
    "Bartter_disease_type_4B|Bartter_disease_type_3|not_provided|Bartter_syndrome|_type_3|_with_hypocalciuria": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|not_specified": 1,
    "BARTTER_SYNDROME|_TYPE_4B|_WITH_SENSORINEURAL_DEAFNESS": 1,
    "Cataract_6_multiple_types": 127,
    "not_provided|Cataract_6_multiple_types": 25,
    "Cataract_6_multiple_types|not_provided": 8,
    "EPHA2-related_disorder": 12,
    "Cataract_6_multiple_types|not_provided|EPHA2-related_disorder|not_specified": 1,
    "EPHA2-related_disorder|not_provided|Cataract_6_multiple_types": 5,
    "not_specified|Cataract_6_multiple_types|not_provided": 2,
    "Cataract_6_multiple_types|EPHA2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cataract_6_multiple_types": 1,
    "EPHA2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|EPHA2-related_disorder": 1,
    "not_specified|not_provided|Cataract_6_multiple_types": 2,
    "Cataract_6_multiple_types|EPHA2-related_disorder": 5,
    "Cataract_6_multiple_types|EPHA2-related_disorder|not_provided": 3,
    "Meniere_disease|EPHA2-related_disorder|not_specified|Cataract_6|_age-related_cortical|Cataract_6_multiple_types": 1,
    "not_provided|Cataract_6_multiple_types|EPHA2-related_disorder": 2,
    "Inborn_genetic_diseases|Cataract_6_multiple_types": 7,
    "not_provided|not_specified|Cataract_6_multiple_types": 2,
    "Developmental_cataract": 51,
    "Age-related_cortical_cataract": 3,
    "Cataract_6_multiple_types|not_provided|not_specified": 3,
    "Cataract_6_multiple_types|Inborn_genetic_diseases": 4,
    "not_provided|EPHA2-related_disorder": 1,
    "not_provided|EPHA2-related_disorder|Cataract_6_multiple_types": 1,
    "EPHA2-related_disorder|Cataract_6_multiple_types": 2,
    "Cataract_6_multiple_types|not_specified|not_provided": 2,
    "not_specified|Cataract_6_multiple_types": 1,
    "Age-related_cortical_cataract|Inborn_genetic_diseases": 1,
    "not_provided|Cataract_6_multiple_types|not_specified": 1,
    "Cataract_6_multiple_types|Meniere_disease": 1,
    "not_provided|Inborn_genetic_diseases|Cataract_6_multiple_types": 1,
    "Cataract_6_multiple_types|not_specified": 1,
    "Cataract|Bilateral_microphthalmos|Congenital_aniridia": 1,
    "Premature_ovarian_insufficiency": 25,
    "Premature_ovarian_insufficiency|not_specified": 1,
    "Kufor-Rakeb_syndrome": 33,
    "ATP13A2-related_disorder|Kufor-Rakeb_syndrome|not_provided": 1,
    "not_provided|Kufor-Rakeb_syndrome": 3,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided": 17,
    "ATP13A2-related_disorder": 5,
    "Kufor-Rakeb_syndrome|ATP13A2-related_disorder|not_provided": 1,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "Kufor-Rakeb_syndrome|not_provided": 4,
    "ATP13A2-related_disorder|not_provided|Kufor-Rakeb_syndrome|Congenital_cerebellar_hypoplasia": 1,
    "not_provided|ATP13A2-related_disorder": 1,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 318,
    "Inborn_genetic_diseases|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided": 6,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 29,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 262,
    "not_provided|ATP13A2-related_disorder|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases": 2,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases": 39,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 2,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 18,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases|not_specified|not_provided": 3,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided|Inborn_genetic_diseases": 3,
    "ATP13A2-related_disorder|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 4,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|not_provided|ATP13A2-related_disorder|Autosomal_recessive_spastic_paraplegia_type_78|not_specified": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases": 21,
    "ATP13A2-related_disorder|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_specified|not_provided": 1,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases|not_provided": 7,
    "Neurodegeneration_with_brain_iron_accumulation": 9,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided": 14,
    "Kufor-Rakeb_syndrome|not_provided|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided": 4,
    "Autosomal_recessive_spastic_paraplegia_type_78|not_provided|Kufor-Rakeb_syndrome|not_specified": 1,
    "not_specified|not_provided|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "not_provided|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 25,
    "not_provided|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases": 8,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_specified": 2,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 9,
    "Autosomal_recessive_spastic_paraplegia_type_78": 7,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 7,
    "not_provided|Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 4,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Neurodegeneration_with_brain_iron_accumulation|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 4,
    "ATP13A2-related_disorder|Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided": 1,
    "ATP13A2-related_disorder|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Parkinsonism_due_to_ATP13A2_deficiency|ATP13A2-related_disorder|not_provided": 1,
    "ATP13A2-related_disorder|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 1,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_specified": 1,
    "Kufor-Rakeb_syndrome|not_specified|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|ATP13A2-related_disorder": 3,
    "ATP13A2-related_disorder|Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 2,
    "Kufor-Rakeb_syndrome|Inborn_genetic_diseases": 1,
    "Kufor-Rakeb_syndrome|Inborn_genetic_diseases|Autosomal_recessive_spastic_paraplegia_type_78|not_provided": 2,
    "Kufor-Rakeb_syndrome|not_specified": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 2,
    "not_provided|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases": 2,
    "ATP13A2-related_disorder|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Kufor-Rakeb_syndrome|not_provided|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "ATP13A2-related_disorder|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "Inborn_genetic_diseases|ATP13A2-related_disorder|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 2,
    "Spastic_tetraparesis": 2,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_specified": 1,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|not_provided|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|See_cases": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|ATP13A2-related_disorder|not_specified": 1,
    "not_specified|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided": 1,
    "ATP13A2-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "not_provided|not_specified|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome": 1,
    "Kufor-Rakeb_syndrome|not_specified|not_provided|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "ATP13A2-related_disorder|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_provided": 1,
    "ATP13A2-related_disorder|not_provided": 1,
    "not_specified|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|ATP13A2-related_disorder|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "not_provided|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases|not_specified": 1,
    "Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|Neurodegeneration_with_brain_iron_accumulation": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases|ATP13A2-related_disorder": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation|Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|ATP13A2-related_disorder|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78": 1,
    "not_provided|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|ATP13A2-related_disorder": 1,
    "Kufor-Rakeb_syndrome|not_provided|Autosomal_recessive_spastic_paraplegia_type_78|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Kufor-Rakeb_syndrome|Autosomal_recessive_spastic_paraplegia_type_78|not_specified|not_provided": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|not_specified|not_provided": 1,
    "Autosomal_recessive_spastic_paraplegia_type_78|Kufor-Rakeb_syndrome|ATP13A2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 2,
    "Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma": 4,
    "Pheochromocytoma/paraganglioma_syndrome_4": 42,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 20,
    "Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma": 10,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 85,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 125,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor": 55,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 100,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor": 7,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 8,
    "Hereditary_pheochromocytoma-paraganglioma": 811,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 109,
    "Gastrointestinal_stromal_tumor": 2988,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 321,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 15,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 5,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided": 6,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 36,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 21,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 25,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 18,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 39,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor": 93,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 9,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome|not_provided": 1,
    "Paragangliome_/_Pheochromocytome": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_specified": 5,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome": 269,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 22,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 7,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 15,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 12,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_4": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome": 3861,
    "Hereditary_cancer-predisposing_syndrome|not_provided": 5106,
    "Paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|SDHB-related_disorder|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 5,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 2,
    "SDHB-related_disorder|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "SDHB-related_disorder|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Cowden_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4": 2,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 2,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Gastrointestinal_stromal_tumor|not_provided|Pheochromocytoma|Ovarian_cancer": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 6,
    "Gastrointestinal_stromal_tumor|Ovarian_cancer": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided": 4,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_pheochromocytoma-paraganglioma": 3,
    "SDHB-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 2,
    "Renal_cell_carcinoma": 1169,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 4,
    "Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4": 5,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 3,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 4,
    "not_provided|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_specified": 2,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|not_specified": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided": 6,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 3,
    "Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 4,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Renal_neoplasm": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome": 1,
    "SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|not_provided|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 3,
    "not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 268,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided": 16,
    "not_provided|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 24,
    "SDHB-related_disorder|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Malignant_tumor_of_breast": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Pheochromocytoma|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor": 10,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|not_provided": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|not_provided|Pheochromocytoma|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Cowden_syndrome|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|not_specified|not_provided": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "SDHB-related_disorder|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma": 10,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|not_specified|not_provided": 1,
    "SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|not_provided|Pheochromocytoma|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Carney_triad|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "SDHB-related_disorder|Gastrointestinal_stromal_tumor|Pheochromocytoma|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|not_provided|SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "SDHB-related_disorder|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|bilateral_breast_cancer": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Von_Hippel-Lindau_syndrome": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHB-related_disorder|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Pheochromocytoma": 9,
    "not_specified|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_specified": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|SDHB-related_disorder": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_4|not_specified|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Gastrointestinal_stromal_tumor|not_provided|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|not_provided": 2,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHB-related_disorder|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|SDHB-related_disorder|Cowden_syndrome|not_provided|not_specified|Carney-Stratakis_syndrome": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4|SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 2,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Cowden_syndrome_1|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|SDHB-related_disorder|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor": 1,
    "SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Carney-Stratakis_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|not_specified": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_4": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "SDHB-related_disorder|Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "SDHB-related_disorder|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Cowden_syndrome|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided|Carney-Stratakis_syndrome": 1,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided": 1,
    "not_specified|Pheochromocytoma|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Paraganglioma|SDHB-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "Gastrointestinal_stromal_tumor|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_4|Mitochondrial_complex_2_deficiency|_nuclear_type_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_specified|not_provided": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_4|Pheochromocytoma|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|SDHB-related_disorder|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_4|Gastrointestinal_stromal_tumor|Pheochromocytoma|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_4|Pheochromocytoma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "not_specified|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|not_specified": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_specified": 6,
    "not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Carney-Stratakis_syndrome": 1,
    "Rheumatoid_arthritis|Abnormal_pulmonary_interstitial_morphology": 4,
    "Rheumatoid_arthritis": 13,
    "PADI3-related_disorder": 14,
    "Uncombable_hair_syndrome_1": 2,
    "PADI3-related_disorder|Uncombable_hair_syndrome_1|not_provided": 1,
    "Central_centrifugal_cicatricial_alopecia": 3,
    "PADI3-related_disorder|not_provided": 1,
    "Central_centrifugal_cicatricial_alopecia|Uncombable_hair_syndrome_1|not_specified": 1,
    "not_provided|PADI3-related_disorder|Uncombable_hair_syndrome_1": 1,
    "Inborn_genetic_diseases|PADI3-related_disorder": 2,
    "Central_centrifugal_cicatricial_alopecia|Uncombable_hair_syndrome_1": 1,
    "Central_centrifugal_cicatricial_alopecia|not_specified": 1,
    "PADI4-related_disorder|not_provided": 1,
    "PADI4-related_disorder|Rheumatoid_arthritis|Abnormal_pulmonary_interstitial_morphology": 4,
    "PADI4-related_disorder": 13,
    "Preimplantation_embryonic_lethality_2": 24,
    "PADI6-related_disorder": 31,
    "not_specified|not_provided|PADI6-related_disorder": 1,
    "PADI6-related_disorder|not_provided": 1,
    "Premature_ovarian_failure": 51,
    "Teratoma": 22,
    "Cerebral_visual_impairment_and_intellectual_disability": 10,
    "Myopathy|_congenital|_progressive|_with_scoliosis": 7,
    "PAX7-related_disorder": 12,
    "Myopathy|_congenital|_progressive|_with_scoliosis|Alveolar_rhabdomyosarcoma": 2,
    "Alveolar_rhabdomyosarcoma|PAX7-related_disorder|See_cases|Myopathy|_congenital|_progressive|_with_scoliosis": 1,
    "PAX7-related_disorder|not_provided": 2,
    "Congenital_myopathy_with_myasthenic-like_onset|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome": 4830,
    "not_provided|Myopathy|_congenital|_progressive|_with_scoliosis": 1,
    "Myopathy|_congenital|_progressive|_with_scoliosis|not_provided": 1,
    "not_provided|PAX7-related_disorder": 1,
    "Hyperprolinemia_type_2|not_provided": 23,
    "Hyperprolinemia_type_2": 209,
    "not_provided|Hyperprolinemia_type_2": 31,
    "Hyperprolinemia": 7,
    "ALDH4A1-related_disorder": 6,
    "not_specified|Hyperprolinemia_type_2": 9,
    "Hyperprolinemia_type_2|ALDH4A1-related_disorder|not_provided": 1,
    "Hyperprolinemia_type_2|not_specified": 7,
    "ALDH4A1-related_disorder|not_provided|Hyperprolinemia_type_2": 3,
    "ALDH4A1-related_disorder|Hyperprolinemia_type_2": 2,
    "not_provided|Hyperprolinemia_type_2|not_specified": 3,
    "not_specified|Intellectual_disability": 22,
    "MHC_class_II_deficiency_1": 12,
    "not_specified|Hyperprolinemia_type_2|ALDH4A1-related_disorder|not_provided": 1,
    "Seizure|not_provided|Hyperprolinemia_type_2": 1,
    "Hyperprolinemia_type_2|ALDH4A1-related_disorder": 1,
    "ALDH4A1-related_disorder|not_provided|Hyperprolinemia_type_2|Intellectual_disability": 1,
    "not_provided|Hyperprolinemia_type_2|Intellectual_disability": 1,
    "Hyperprolinemia_type_2|Intellectual_disability": 1,
    "Hyperprolinemia_type_2|not_provided|not_specified": 1,
    "not_provided|ALDH4A1-related_disorder|Hyperprolinemia_type_2": 1,
    "not_provided|Hyperprolinemia_type_2|ALDH4A1-related_disorder": 1,
    "UBR4-related_disorder|not_provided": 34,
    "UBR4-related_disorder": 41,
    "not_provided|not_specified|UBR4-related_disorder": 1,
    "not_provided|UBR4-related_disorder": 14,
    "Short_stature|not_specified": 10,
    "not_provided|UBR4-related_disorder|Short_stature": 1,
    "Short_stature": 103,
    "not_specified|UBR4-related_disorder": 3,
    "not_specified|UBR4-associated_neurodevelopmental_syndrome|Short_stature": 1,
    "not_specified|UBR4-associated_neurodevelopmental_syndrome": 1,
    "not_specified|EMC1-related_disorder|not_provided|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 1,
    "Cerebellar_atrophy|Global_developmental_delay|not_provided": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 17,
    "not_provided|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 12,
    "not_provided|Microcephaly": 10,
    "EMC1-related_disorder|not_provided": 5,
    "not_provided|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 29,
    "EMC1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|not_provided": 14,
    "not_provided|EMC1-related_disorder": 5,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Inborn_genetic_diseases": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|not_provided|Retinal_dystrophy": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Retinal_dystrophy": 1,
    "EMC1-related_disorder|not_provided|not_specified": 1,
    "not_specified|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 38,
    "Inborn_genetic_diseases|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Retinal_dystrophy|not_provided": 1,
    "not_provided|Global_developmental_delay|Cerebellar_atrophy": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Retinal_dystrophy|not_provided|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 1,
    "Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Retinal_dystrophy|not_provided": 2,
    "not_provided|Retinal_dystrophy|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 2,
    "Retinal_dystrophy|EMC1-related_disorder|not_provided": 1,
    "See_cases|not_provided|Inborn_genetic_diseases": 3,
    "Retinal_dystrophy|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 1,
    "not_provided|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B": 1,
    "not_provided|Obesity": 8,
    "EMC1-related_disorder|not_provided|Cerebellar_atrophy|_visual_impairment|_and_psychomotor_retardation%3B|Inborn_genetic_diseases|not_specified": 1,
    "Retinal_dystrophy|not_provided|Inborn_genetic_diseases": 43,
    "Nephropathic_cystinosis": 64,
    "PLA2G2A-related_disorder": 4,
    "Familial_colorectal_cancer": 987,
    "not_provided|PLA2G2A-related_disorder": 1,
    "not_provided|Familial_benign_flecked_retina": 3,
    "Familial_benign_flecked_retina": 2,
    "Late-onset_retinal_degeneration": 6,
    "not_provided|Familial_benign_flecked_retina|not_specified": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6": 239,
    "Inborn_genetic_diseases|Autosomal_recessive_early-onset_Parkinson_disease_6": 6,
    "PINK1-related_disorder|not_specified|Autosomal_recessive_early-onset_Parkinson_disease_6": 1,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6": 23,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6|See_cases": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|Inborn_genetic_diseases": 6,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6|not_specified": 2,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|not_provided": 24,
    "not_specified|not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6": 2,
    "not_provided|PINK1-Related_Parkinsonism|Autosomal_recessive_early-onset_Parkinson_disease_6": 1,
    "PINK1-related_disorder|Autosomal_recessive_early-onset_Parkinson_disease_6|not_provided": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|not_specified": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|not_provided|See_cases": 1,
    "PINK1-related_disorder|not_specified|Autosomal_recessive_early-onset_Parkinson_disease_6|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_early-onset_Parkinson_disease_6": 1,
    "PINK1-related_disorder|Autosomal_recessive_early-onset_Parkinson_disease_6": 1,
    "PINK1-related_disorder|not_specified|not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6": 2,
    "not_provided|PINK1-related_disorder|Autosomal_recessive_early-onset_Parkinson_disease_6|not_specified": 1,
    "PINK1-related_disorder": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|not_provided|not_specified": 1,
    "PINK1-related_disorder|not_provided|not_specified|Autosomal_recessive_early-onset_Parkinson_disease_6": 1,
    "Parkinson_disease_6": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|PINK1-related_disorder": 2,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6|PINK1-related_disorder": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|PINK1-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6|Inborn_genetic_diseases": 1,
    "not_provided|Parkinson_Disease|_Recessive|Autosomal_recessive_early-onset_Parkinson_disease_6|Congenital_disorder_of_glycosylation|not_specified": 1,
    "not_provided|Parkinson_Disease|_Recessive|Congenital_disorder_of_glycosylation|Autosomal_recessive_early-onset_Parkinson_disease_6|not_specified": 1,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6|Parkinson_Disease|_Recessive|Congenital_disorder_of_glycosylation": 4,
    "Congenital_disorder_of_glycosylation|not_provided|Autosomal_recessive_early-onset_Parkinson_disease_6|Parkinson_Disease|_Recessive": 1,
    "not_provided|Parkinson_Disease|_Recessive|Autosomal_recessive_early-onset_Parkinson_disease_6|Congenital_disorder_of_glycosylation": 1,
    "Parkinson_Disease|_Recessive|not_provided": 2,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|Parkinson_Disease|_Recessive": 1,
    "Congenital_disorder_of_glycosylation|Parkinson_Disease|_Recessive": 3,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|not_provided|Parkinson_Disease|_Recessive|Congenital_disorder_of_glycosylation": 1,
    "Parkinson_Disease|_Recessive|Congenital_disorder_of_glycosylation": 2,
    "Leprosy|_susceptibility_to|_1": 13,
    "Congenital_disorder_of_glycosylation": 327,
    "Congenital_disorder_of_glycosylation|not_provided": 21,
    "Congenital_disorder_of_glycosylation|Parkinson_Disease|_Recessive|not_provided|Congenital_disorder_of_glycosylation_type_Ir": 1,
    "DDOST-related_disorder": 4,
    "Congenital_disorder_of_glycosylation_type_Ir": 125,
    "not_specified|Congenital_disorder_of_glycosylation_type_Ir": 17,
    "Congenital_disorder_of_glycosylation_type_Ir|DDOST-related_disorder": 2,
    "Congenital_disorder_of_glycosylation_type_Ir|not_provided": 5,
    "Congenital_disorder_of_glycosylation_type_Ir|not_specified": 14,
    "not_provided|Congenital_disorder_of_glycosylation_type_Ir": 7,
    "DDOST-related_disorder|not_provided|Congenital_disorder_of_glycosylation_type_Ir": 1,
    "not_provided|Congenital_disorder_of_glycosylation_type_Ir|not_specified": 1,
    "DDOST-related_disorder|not_provided|Congenital_disorder_of_glycosylation|Parkinson_Disease|_Recessive|Congenital_disorder_of_glycosylation_type_Ir|not_specified": 1,
    "not_specified|not_provided|Congenital_disorder_of_glycosylation_type_Ir": 4,
    "Congenital_disorder_of_glycosylation_type_Ir|DDOST-related_disorder|not_specified": 1,
    "not_specified|Congenital_disorder_of_glycosylation_type_Ir|not_provided|DDOST-related_disorder": 1,
    "Congenital_disorder_of_glycosylation_type_Ir|not_provided|not_specified": 1,
    "DDOST-related_disorder|Congenital_disorder_of_glycosylation_type_Ir": 1,
    "Congenital_disorder_of_glycosylation|not_specified|not_provided|Parkinson_Disease|_Recessive|Congenital_disorder_of_glycosylation_type_Ir": 1,
    "Congenital_disorder_of_glycosylation_type_Ir|Congenital_disorder_of_glycosylation": 1,
    "DDOST-related_disorder|not_specified|not_provided|Congenital_disorder_of_glycosylation_type_Ir": 1,
    "not_specified|Congenital_disorder_of_glycosylation_type_Ir|not_provided": 1,
    "not_provided|DDOST-related_disorder|not_specified|Congenital_disorder_of_glycosylation_type_Ir": 1,
    "KIF17-related_disorder": 4,
    "not_specified|KIF17-related_disorder": 1,
    "Heparin_cofactor_II_deficiency": 12,
    "Hirschsprung_disease|_cardiac_defects|_and_autonomic_dysfunction": 3,
    "ECE1-related_disorder": 8,
    "Aganglionic_megacolon": 45,
    "Essential_hypertension|_genetic|Hirschsprung_disease|_cardiac_defects|_and_autonomic_dysfunction": 1,
    "not_provided|ECE1-related_disorder": 2,
    "not_specified|Hirschsprung_disease|_cardiac_defects|_and_autonomic_dysfunction": 1,
    "Hypertension|_essential|_susceptibility_to": 2,
    "ALPL-related_disorder": 6,
    "Hypophosphatasia": 255,
    "Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Decreased_circulating_alkaline_phosphatase_activity": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided": 15,
    "not_provided|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 7,
    "Hypophosphatasia|not_provided": 64,
    "Infantile_hypophosphatasia|Hypophosphatasia|Adult_hypophosphatasia": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|Inborn_genetic_diseases": 1,
    "not_provided|Hypophosphatasia": 64,
    "Hypophosphatasia|not_provided|Infantile_hypophosphatasia": 1,
    "ALPL-related_disorder|not_provided|Hypophosphatasia": 2,
    "Infantile_hypophosphatasia|Hypophosphatasia": 6,
    "Infantile_hypophosphatasia|ALPL-related_disorder": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 13,
    "ALPL-related_disorder|not_provided": 8,
    "Adult_hypophosphatasia": 18,
    "Hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia": 2,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 35,
    "not_provided|Infantile_hypophosphatasia": 9,
    "Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided": 6,
    "Hypophosphatasia|See_cases|not_provided|ALPL-related_disorder|Adult_hypophosphatasia": 1,
    "Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|not_provided|Hypophosphatasia": 2,
    "not_provided|Hypophosphatasia|ALPL-related_disorder": 1,
    "not_provided|Hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia": 2,
    "Hypophosphatasia|not_provided|ALPL-related_disorder|Adult_hypophosphatasia": 1,
    "Infantile_hypophosphatasia": 12,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|ALPL-related_disorder": 2,
    "Adult_hypophosphatasia|not_provided": 4,
    "Hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|not_provided": 1,
    "Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 2,
    "Hypophosphatasia|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|Infantile_hypophosphatasia": 1,
    "Adult_hypophosphatasia|Hypophosphatasia|not_provided": 7,
    "not_provided|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 2,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|Inborn_genetic_diseases": 1,
    "not_provided|Hypophosphatasia|not_specified": 5,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided": 3,
    "not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia": 10,
    "Osteogenesis_imperfecta|not_provided": 37,
    "ALPL-related_disorder|not_provided|Hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Hypophosphatasia|not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia": 4,
    "not_provided|Hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 6,
    "not_provided|Hypophosphatasia|Adult_hypophosphatasia": 9,
    "ALPL-related_disorder|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "Hypophosphatasia|not_provided|Adult_hypophosphatasia": 6,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "not_provided|Osteogenesis_imperfecta|Adult_hypophosphatasia|Hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|not_specified|Infantile_hypophosphatasia": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Decreased_circulating_alkaline_phosphatase_activity|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "Adult_hypophosphatasia|Hypophosphatasia": 6,
    "not_provided|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|ALPL-related_disorder": 1,
    "not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|ALPL-related_disorder|not_provided": 1,
    "Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "ALPL-related_disorder|Hypophosphatasia|not_provided": 2,
    "not_provided|Infantile_hypophosphatasia|Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 2,
    "Hypophosphatasia|Odontohypophosphatasia": 1,
    "not_specified|not_provided|Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "not_provided|not_specified|Adult_hypophosphatasia|Hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 6,
    "Hypophosphatasia|not_provided|not_specified": 3,
    "ALPL-related_disorder|Hypophosphatasia|not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia|Odontohypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_provided|Adult_hypophosphatasia": 3,
    "not_provided|not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia": 1,
    "Infantile_hypophosphatasia|not_provided": 2,
    "not_provided|Adult_hypophosphatasia|Hypophosphatasia": 2,
    "Adult_hypophosphatasia|Hypophosphatasia|not_specified": 1,
    "Childhood_hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 7,
    "Adult_hypophosphatasia|not_provided|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia": 1,
    "Hypophosphatemia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "Hypophosphatasia|not_provided|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 2,
    "not_provided|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia|Osteogenesis_imperfecta|Odontohypophosphatasia": 1,
    "Hypophosphatasia|Infantile_hypophosphatasia|not_provided": 2,
    "ALPL-related_disorder|Inborn_genetic_diseases|not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia": 3,
    "not_provided|ALPL-related_disorder|Hypophosphatasia|not_specified": 1,
    "not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 4,
    "not_provided|Infantile_hypophosphatasia|Hypophosphatasia": 3,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 5,
    "Inborn_genetic_diseases|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "Hypophosphatasia|not_specified|not_provided": 1,
    "Childhood_hypophosphatasia|not_provided": 2,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|Osteogenesis_imperfecta|not_provided|Hypophosphatasia": 1,
    "not_specified|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|not_provided|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "Infantile_hypophosphatasia|Adult_hypophosphatasia|not_provided|Childhood_hypophosphatasia": 1,
    "not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Decreased_circulating_alkaline_phosphatase_activity|not_provided": 1,
    "Adult_hypophosphatasia|not_provided|Inborn_genetic_diseases": 1,
    "Hypophosphatasia|not_provided|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Hypophosphatasia|not_provided|ALPL-related_disorder|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|not_provided": 3,
    "Hypophosphatasia|ALPL-related_disorder": 1,
    "ALPL-related_disorder|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|not_provided|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia|Inborn_genetic_diseases|not_specified|Hypophosphatasia|Microcephaly|Childhood_hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Decreased_circulating_alkaline_phosphatase_activity|not_specified|not_provided": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Micromelia|Hypophosphatasia": 1,
    "not_specified|Hypophosphatasia": 2,
    "Inborn_genetic_diseases|not_provided|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 2,
    "Inborn_genetic_diseases|not_provided|Hypophosphatasia|Osteogenesis_imperfecta|Odontohypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia": 1,
    "Hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided": 2,
    "ALPL-related_disorder|Inborn_genetic_diseases|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|Osteogenesis_imperfecta|Odontohypophosphatasia|See_cases": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|ALPL-related_disorder": 1,
    "Adult_hypophosphatasia|not_provided|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 2,
    "not_provided|Inborn_genetic_diseases|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "not_specified|not_provided|Hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|not_specified": 1,
    "not_provided|not_specified|Hypophosphatasia|Infantile_hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Infantile_hypophosphatasia": 5,
    "Hypophosphatasia|not_provided|ALPL-related_disorder": 2,
    "ALPL-related_disorder|Adult_hypophosphatasia|Childhood_hypophosphatasia|Inborn_genetic_diseases|Perinatal_lethal_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "not_provided|Micromelia": 1,
    "not_provided|Infantile_hypophosphatasia|not_specified": 1,
    "not_provided|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_specified": 2,
    "not_provided|Hypophosphatasia|ALPL-related_disorder|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|not_provided|Infantile_hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_provided|Infantile_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Osteogenesis_imperfecta|Hypophosphatasia|not_provided": 1,
    "Adult_hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Hypophosphatasia": 1,
    "Hypophosphatasia|ALPL-related_disorder|not_provided": 2,
    "ALPL-related_disorder|not_provided|Hypophosphatasia|Adult_hypophosphatasia|Odontohypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_provided|not_specified|Hypophosphatasia|Infantile_hypophosphatasia|Osteogenesis_imperfecta|Childhood_hypophosphatasia|Adult_hypophosphatasia": 1,
    "not_specified|not_provided|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "Infantile_hypophosphatasia|not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_specified|not_provided|Hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_provided|Decreased_circulating_alkaline_phosphatase_activity": 1,
    "ALPL-related_disorder|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Hypophosphatasia|not_provided|Osteogenesis_imperfecta|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "ALPL-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hypophosphatasia": 1,
    "ALPL-related_disorder|not_provided|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Adult_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia": 1,
    "Hypophosphatasia|Childhood_hypophosphatasia|not_specified|not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Childhood_hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|not_provided|Infantile_hypophosphatasia|Childhood_hypophosphatasia": 2,
    "Hypophosphatasia|Childhood_hypophosphatasia|not_specified|not_provided|Infantile_hypophosphatasia|Adult_hypophosphatasia": 1,
    "Infantile_hypophosphatasia|not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "not_specified|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "Hypophosphatasia|Infantile_hypophosphatasia|not_specified|not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Adult_hypophosphatasia|Decreased_circulating_alkaline_phosphatase_activity": 1,
    "ALPL-related_disorder|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|not_provided|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "Hypophosphatasia|Inborn_genetic_diseases|not_provided|Adult_hypophosphatasia": 1,
    "ALPL-related_disorder|Multiple_epiphyseal_dysplasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Adult_hypophosphatasia|not_provided|Hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Infantile_hypophosphatasia|Hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|not_provided": 1,
    "Hypophosphatasia|not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|ALPL-related_disorder|Inborn_genetic_diseases|Hypophosphatasia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "ALPL-related_disorder|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 2,
    "not_provided|Osteogenesis_imperfecta|Hypophosphatasia|Adult_hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Inborn_genetic_diseases|Adult_hypophosphatasia": 1,
    "ALPL-related_disorder|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|Osteogenesis_imperfecta": 1,
    "not_specified|Hypophosphatasia|not_provided": 1,
    "Adult_hypophosphatasia|not_provided|ALPL-related_disorder|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|not_provided|Hypophosphatasia|ALPL-related_disorder": 1,
    "not_provided|Hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia": 2,
    "not_provided|Infantile_hypophosphatasia|ALPL-related_disorder|not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Hypophosphatasia": 1,
    "Hypophosphatasia|Inborn_genetic_diseases": 1,
    "not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia": 3,
    "not_provided|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|Connective_tissue_disorder": 1,
    "not_provided|ALPL-related_disorder": 1,
    "Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia|not_provided": 2,
    "Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|not_specified|not_provided|Decreased_circulating_alkaline_phosphatase_activity": 1,
    "Hypophosphatasia|Infantile_hypophosphatasia|not_provided|Adult_hypophosphatasia": 1,
    "not_provided|Osteogenesis_imperfecta": 41,
    "not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Osteogenesis_imperfecta": 1,
    "not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia|Decreased_circulating_alkaline_phosphatase_activity|Childhood_hypophosphatasia|Hypophosphatasia": 1,
    "Osteogenesis_imperfecta|not_provided|Hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_provided|Hypophosphatasia|ALPL-related_disorder": 1,
    "ALPL-related_disorder|Inborn_genetic_diseases|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "not_provided|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|not_provided|Hypophosphatasia": 2,
    "Hypophosphatasia|not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|not_specified": 1,
    "Hypophosphatasia|not_provided|ALPL-related_disorder|Inborn_genetic_diseases|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Osteogenesis_imperfecta": 1,
    "Hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "Childhood_hypophosphatasia|Hypophosphatasia|not_provided|Adult_hypophosphatasia": 1,
    "not_provided|Inborn_genetic_diseases|Hypophosphatasia": 1,
    "Infantile_hypophosphatasia|not_specified|not_provided|Hypophosphatasia": 1,
    "Decreased_circulating_alkaline_phosphatase_activity": 4,
    "Hypophosphatasia|not_provided|Adult_hypophosphatasia|ALPL-related_disorder": 1,
    "ALPL-related_disorder|Perinatal_lethal_hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|not_provided|Hypophosphatasia": 1,
    "Adult_hypophosphatasia|not_provided|Hypophosphatasia": 2,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Hypophosphatasia|not_provided": 1,
    "Hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|Hypophosphatasia": 1,
    "Infantile_hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|not_specified|not_provided|Hypophosphatasia": 1,
    "not_specified|Hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia|not_specified|not_provided": 1,
    "Hypophosphatasia|Osteogenesis_imperfecta|ALPL-related_disorder|not_specified|not_provided": 1,
    "Hypophosphatasia|Adult_hypophosphatasia|ALPL-related_disorder|Decreased_circulating_alkaline_phosphatase_activity|not_provided": 1,
    "Infantile_hypophosphatasia|Inborn_genetic_diseases|Adult_hypophosphatasia|Childhood_hypophosphatasia|Hypophosphatasia|not_provided|ALPL-related_disorder": 1,
    "Childhood_hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|ALPL-related_disorder|Adult_hypophosphatasia|not_specified": 1,
    "Hypophosphatasia|not_provided|Adult_hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_specified|Decreased_circulating_alkaline_phosphatase_activity": 1,
    "Decreased_circulating_alkaline_phosphatase_activity|not_specified|not_provided": 1,
    "not_provided|Childhood_hypophosphatasia|Hypophosphatasia|Infantile_hypophosphatasia|Adult_hypophosphatasia": 1,
    "Inborn_genetic_diseases|Hypophosphatasia|not_specified|not_provided": 1,
    "not_provided|Adult_hypophosphatasia|ALPL-related_disorder|Hypophosphatasia": 1,
    "Hypophosphatasia|Infantile_hypophosphatasia|not_provided|Adult_hypophosphatasia|Childhood_hypophosphatasia": 1,
    "Hypophosphatasia|Childhood_hypophosphatasia": 1,
    "not_provided|Hypophosphatasia|Osteogenesis_imperfecta|Adult_hypophosphatasia|Childhood_hypophosphatasia|Infantile_hypophosphatasia": 1,
    "not_provided|Infantile_hypophosphatasia|not_specified|Adult_hypophosphatasia|Childhood_hypophosphatasia|Hypophosphatasia": 1,
    "Hypophosphatasia|not_specified|Osteogenesis_imperfecta|not_provided": 1,
    "Infantile_hypophosphatasia|Decreased_circulating_alkaline_phosphatase_activity": 1,
    "Childhood_hypophosphatasia|Adult_hypophosphatasia|Infantile_hypophosphatasia|ALPL-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Hypophosphatasia|Infantile_hypophosphatasia|Childhood_hypophosphatasia|Adult_hypophosphatasia": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta|not_provided|Infantile_hypophosphatasia": 1,
    "USP48-related_condition": 4,
    "Hearing_loss|_autosomal_dominant_85": 3,
    "Schwartz-Jampel_syndrome_type_1": 25,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 18,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 43,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 54,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 78,
    "Schwartz-Jampel_syndrome|not_provided|Lethal_Kniest-like_syndrome": 17,
    "not_provided|Microcephaly|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Connective_tissue_disorder|not_provided": 41,
    "Inborn_genetic_diseases|not_provided|HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Lethal_Kniest-like_syndrome": 14,
    "not_provided|Connective_tissue_disorder|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "not_provided|Lethal_Kniest-like_syndrome|HSPG2-related_disorder|Schwartz-Jampel_syndrome": 1,
    "not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 32,
    "Inborn_genetic_diseases|HSPG2-related_disorder|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder": 1,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder|Inborn_genetic_diseases|Schwartz-Jampel_syndrome_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 6,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_provided": 11,
    "HSPG2-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Lethal_Kniest-like_syndrome|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 2,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|HSPG2-related_disorder|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|HSPG2-related_disorder": 1,
    "HSPG2-related_disorder": 14,
    "not_specified|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|not_specified|Connective_tissue_disorder": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 5,
    "not_specified|HSPG2-related_disorder|not_provided": 2,
    "not_provided|Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 5,
    "Connective_tissue_disorder": 143,
    "Schwartz-Jampel_syndrome|not_provided": 3,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided": 8,
    "not_provided|Lethal_Kniest-like_syndrome": 2,
    "HSPG2-related_disorder|not_provided": 13,
    "Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Connective_tissue_disorder|not_provided|HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Schwartz-Jampel_syndrome|Connective_tissue_disorder|not_provided|Lethal_Kniest-like_syndrome": 3,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|not_specified": 216,
    "Lethal_Kniest-like_syndrome|HSPG2-related_disorder|Schwartz-Jampel_syndrome|not_provided": 1,
    "Lethal_Kniest-like_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|HSPG2-related_disorder|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_provided|not_specified": 4,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|not_specified": 4,
    "not_provided|HSPG2-related_disorder": 17,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|not_provided": 2,
    "HSPG2-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 2,
    "Connective_tissue_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome": 13,
    "not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|HSPG2-related_disorder|Inborn_genetic_diseases|not_provided|Schwartz-Jampel_syndrome": 1,
    "HSPG2-related_disorder|not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1": 3,
    "Schwartz-Jampel_syndrome": 9,
    "not_specified|Inborn_genetic_diseases|HSPG2-related_disorder|not_provided": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|HSPG2-related_disorder|not_provided": 3,
    "Lethal_Kniest-like_syndrome|not_provided|Schwartz-Jampel_syndrome|not_specified": 2,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Schwartz-Jampel_syndrome_type_1": 1,
    "Lethal_Kniest-like_syndrome|not_provided|Schwartz-Jampel_syndrome|Connective_tissue_disorder": 1,
    "HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 2,
    "Connective_tissue_disorder|not_specified|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 2,
    "not_specified|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 8,
    "not_specified|Lethal_Kniest-like_syndrome|Connective_tissue_disorder|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|Schwartz-Jampel_syndrome|Connective_tissue_disorder|Lethal_Kniest-like_syndrome|not_specified": 2,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Inborn_genetic_diseases": 4,
    "Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome|not_provided": 1,
    "Microcephaly|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome": 1,
    "Lethal_Kniest-like_syndrome|not_provided|Schwartz-Jampel_syndrome": 6,
    "Schwartz-Jampel_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|not_specified": 1,
    "Lethal_Kniest-like_syndrome|Stuve-Wiedemann_syndrome|not_provided|Schwartz-Jampel_syndrome|Reduced_muscle_fiber_perlecan": 1,
    "HSPG2-related_disorder|not_provided|not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome|not_provided|Connective_tissue_disorder|Lethal_Kniest-like_syndrome": 1,
    "not_specified|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Connective_tissue_disorder|not_provided": 1,
    "HSPG2-related_disorder|Connective_tissue_disorder|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_specified": 1,
    "Schwartz-Jampel_syndrome|not_provided|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|Inborn_genetic_diseases": 5,
    "Lethal_Kniest-like_syndrome|Microcephaly|not_provided|Schwartz-Jampel_syndrome|Inborn_genetic_diseases": 1,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Connective_tissue_disorder|not_specified|not_provided": 1,
    "not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 2,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Connective_tissue_disorder|HSPG2-related_disorder|not_specified|not_provided|Schwartz-Jampel_syndrome": 1,
    "Inborn_genetic_diseases|Schwartz-Jampel_syndrome|not_provided|Lethal_Kniest-like_syndrome": 6,
    "Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 4,
    "Lethal_Kniest-like_syndrome|HSPG2-related_disorder|Schwartz-Jampel_syndrome|Schwartz-Jampel_syndrome_type_1|not_specified|not_provided": 1,
    "Microcephaly|not_provided": 12,
    "Inborn_genetic_diseases|not_specified|not_provided|HSPG2-related_disorder": 1,
    "not_specified|not_provided|Schwartz-Jampel_syndrome|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome": 1,
    "not_provided|HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome|not_provided": 1,
    "Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "not_provided|Lethal_Kniest-like_syndrome|not_specified|Schwartz-Jampel_syndrome": 2,
    "Schwartz-Jampel_syndrome_type_1|not_provided": 4,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|Schwartz-Jampel_syndrome_type_1": 1,
    "Schwartz-Jampel_syndrome|Schwartz-Jampel_syndrome_type_1": 1,
    "Connective_tissue_disorder|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "not_specified|not_provided|Connective_tissue_disorder": 10,
    "Abnormal_facial_shape": 1,
    "not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 3,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_specified|Schwartz-Jampel_syndrome|not_provided|Inborn_genetic_diseases|HSPG2-related_disorder": 1,
    "not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder|not_provided": 2,
    "not_specified|Connective_tissue_disorder|not_provided": 9,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided|Schwartz-Jampel_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|HSPG2-related_disorder": 2,
    "not_provided|Abnormal_facial_shape": 1,
    "Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided": 2,
    "HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided": 1,
    "Schwartz-Jampel_syndrome|not_provided|HSPG2-related_disorder|Lethal_Kniest-like_syndrome": 1,
    "Connective_tissue_disorder|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Schwartz-Jampel_syndrome|not_provided|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome": 1,
    "not_provided|Schwartz-Jampel_syndrome|See_cases|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|See_cases": 11,
    "Schwartz-Jampel_syndrome|not_specified|not_provided|HSPG2-related_disorder|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome": 1,
    "not_provided|not_specified|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "not_specified|HSPG2-related_disorder|Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 1,
    "not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|HSPG2-related_disorder": 1,
    "Connective_tissue_disorder|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_provided": 1,
    "not_provided|Schwartz-Jampel_syndrome": 2,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "HSPG2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Lethal_Kniest-like_syndrome|Inborn_genetic_diseases|Schwartz-Jampel_syndrome": 3,
    "not_specified|HSPG2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder|not_provided|Schwartz-Jampel_syndrome_type_1": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1": 2,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|HSPG2-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome": 1,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder": 2,
    "not_provided|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases": 1,
    "HSPG2-related_disorder|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|not_provided|not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Schwartz-Jampel_syndrome|HSPG2-related_disorder|Connective_tissue_disorder|Lethal_Kniest-like_syndrome": 1,
    "not_specified|Lethal_Kniest-like_syndrome|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|HSPG2-related_disorder|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 1,
    "Schwartz-Jampel_syndrome|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome": 1,
    "not_provided|Lethal_Kniest-like_syndrome|Connective_tissue_disorder|Schwartz-Jampel_syndrome": 1,
    "Inborn_genetic_diseases|Connective_tissue_disorder|not_provided": 5,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_perlecan": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 2,
    "Lethal_Kniest-like_syndrome|Inborn_genetic_diseases|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome": 1,
    "Schwartz-Jampel_syndrome_type_1|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 2,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Connective_tissue_disorder|not_provided|Inborn_genetic_diseases|Schwartz-Jampel_syndrome": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Intellectual_disability": 27,
    "not_provided|Schwartz-Jampel_syndrome_type_1": 1,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Schwartz-Jampel_syndrome|Connective_tissue_disorder|Lethal_Kniest-like_syndrome": 1,
    "Inborn_genetic_diseases|HSPG2-related_disorder|not_specified|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Microcephaly": 121,
    "Inborn_genetic_diseases|Schwartz-Jampel_syndrome": 1,
    "HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 2,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided|Connective_tissue_disorder|not_specified": 2,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_specified|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|Connective_tissue_disorder|Inborn_genetic_diseases": 3,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Schwartz-Jampel_syndrome|Connective_tissue_disorder|Lethal_Kniest-like_syndrome": 1,
    "Connective_tissue_disorder|HSPG2-related_disorder|Lethal_Kniest-like_syndrome|not_provided|not_specified|Schwartz-Jampel_syndrome": 1,
    "Schwartz-Jampel_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Lethal_Kniest-like_syndrome": 1,
    "Lethal_Kniest-like_syndrome|not_specified|not_provided|Connective_tissue_disorder|Schwartz-Jampel_syndrome": 1,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_specified": 1,
    "not_specified|not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "HSPG2-related_disorder|Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_specified|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Schwartz-Jampel_syndrome_type_1": 1,
    "not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Connective_tissue_disorder|not_specified": 1,
    "Schwartz-Jampel_syndrome|Inborn_genetic_diseases|not_provided|Lethal_Kniest-like_syndrome": 3,
    "Schwartz-Jampel_syndrome|HSPG2-related_disorder|not_specified|not_provided|Lethal_Kniest-like_syndrome": 1,
    "HSPG2-related_disorder|not_specified|not_provided": 1,
    "Schwartz-Jampel_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Lethal_Kniest-like_syndrome|Connective_tissue_disorder|Schwartz-Jampel_syndrome|HSPG2-related_disorder|not_provided|not_specified": 1,
    "not_provided|Connective_tissue_disorder": 55,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1": 1,
    "HSPG2-related_disorder|not_specified|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 2,
    "not_provided|HSPG2-related_disorder|Lethal_Kniest-like_syndrome": 1,
    "HSPG2-related_disorder|not_specified|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Intellectual_disability": 1,
    "not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1": 1,
    "HSPG2-related_disorder|not_provided|not_specified": 1,
    "HSPG2-related_disorder|not_specified|Connective_tissue_disorder|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Multiple_congenital_anomalies/dysmorphic_syndrome|HSPG2-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Schwartz-Jampel_syndrome|not_provided|not_specified|Lethal_Kniest-like_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|HSPG2-related_disorder": 2,
    "HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_specified|not_provided": 1,
    "Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome": 1,
    "Childhood-onset_schizophrenia|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_specified|not_provided": 1,
    "not_specified|HSPG2-related_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_provided": 2,
    "HSPG2-realted_disorder": 2,
    "Lethal_Kniest-like_syndrome|not_provided|HSPG2-related_disorder|Schwartz-Jampel_syndrome": 1,
    "Lethal_Kniest-like_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "HSPG2-related_disorder|Connective_tissue_disorder|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Schwartz-Jampel_syndrome_type_1|not_specified|not_provided": 1,
    "HSPG2-related_disorder|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Multiple_congenital_anomalies/dysmorphic_syndrome|Connective_tissue_disorder": 1,
    "not_provided|Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 2,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Schwartz-Jampel_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|not_specified|Schwartz-Jampel_syndrome_type_1": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Connective_tissue_disorder|not_provided|Schwartz-Jampel_syndrome|not_specified": 1,
    "not_provided|Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases": 1,
    "Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Inborn_genetic_diseases|not_provided|Schwartz-Jampel_syndrome|HSPG2-related_disorder|Connective_tissue_disorder": 1,
    "HSPG2-related_disorder|not_provided|not_specified|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases|not_provided|not_specified|Schwartz-Jampel_syndrome": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Schwartz-Jampel_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_provided|Schwartz-Jampel_syndrome_type_1": 1,
    "not_provided|Connective_tissue_disorder|not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 1,
    "not_provided|HSPG2-related_disorder|Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome": 1,
    "HSPG2-related_disorder|Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|not_provided": 1,
    "not_provided|not_specified|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome": 2,
    "Lethal_Kniest-like_syndrome|Inborn_genetic_diseases|Schwartz-Jampel_syndrome|not_provided": 1,
    "not_specified|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_provided": 1,
    "not_provided|HSPG2-related_disorder|Connective_tissue_disorder|not_specified": 1,
    "not_specified|not_provided|HSPG2-related_disorder|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Connective_tissue_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Schwartz-Jampel_syndrome": 1,
    "HSPG2-related_disorder|Connective_tissue_disorder|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|not_specified|not_provided": 1,
    "HSPG2-related_disorder|not_specified|not_provided|Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases|not_specified|not_provided|Schwartz-Jampel_syndrome": 1,
    "Inborn_genetic_diseases|Schwartz-Jampel_syndrome_type_1|not_provided": 1,
    "not_provided|Schwartz-Jampel_syndrome_type_1|Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Schwartz-Jampel_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Schwartz-Jampel_syndrome|Lethal_Kniest-like_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Schwartz-Jampel_syndrome|Chromosome_1p36_deletion_syndrome|Inborn_genetic_diseases|Lethal_Kniest-like_syndrome|not_provided": 1,
    "Lethal_Kniest-like_syndrome|Schwartz-Jampel_syndrome|HSPG2-related_disorder|not_provided|not_specified": 1,
    "Neurodevelopmental_abnormality|Postnatal_growth_retardation|Abnormality_of_blood_and_blood-forming_tissues|Abnormality_of_the_immune_system|Abnormal_facial_shape|not_provided|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome": 1,
    "Congenital_heart_disease": 44,
    "CDC42-related_disorder|Neurodevelopmental_disorder|Inborn_genetic_diseases|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|not_provided|Abnormality_of_the_immune_system|Neurodevelopmental_abnormality|Abnormal_facial_shape|Abnormality_of_blood_and_blood-forming_tissues|Postnatal_growth_retardation": 1,
    "Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|not_provided|CDC42-related_disorder": 1,
    "not_provided|CDC42-related_disorder": 1,
    "Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome": 6,
    "Inborn_genetic_diseases|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|not_provided|Abnormality_of_the_immune_system|Neurodevelopmental_abnormality|Abnormal_facial_shape|Abnormality_of_blood_and_blood-forming_tissues|Postnatal_growth_retardation": 1,
    "Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|Inborn_genetic_diseases|Abnormality_of_the_immune_system|Abnormality_of_blood_and_blood-forming_tissues|Neurodevelopmental_abnormality|Postnatal_growth_retardation|Abnormal_facial_shape|not_provided": 1,
    "Postnatal_growth_retardation|Abnormal_facial_shape|Neurodevelopmental_abnormality|Abnormality_of_blood_and_blood-forming_tissues|Abnormality_of_the_immune_system|not_provided|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome": 1,
    "Abnormality_of_the_immune_system|Postnatal_growth_retardation|Neurodevelopmental_abnormality|Abnormal_facial_shape|Abnormality_of_blood_and_blood-forming_tissues|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|not_provided": 1,
    "Abnormal_facial_shape|Abnormality_of_the_immune_system|Neurodevelopmental_abnormality|Postnatal_growth_retardation|Abnormality_of_blood_and_blood-forming_tissues|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|not_provided": 1,
    "CDC42-related_disorder": 2,
    "Abnormal_facial_shape|Abnormality_of_the_immune_system|Neurodevelopmental_abnormality|Postnatal_growth_retardation|Abnormality_of_blood_and_blood-forming_tissues|not_provided": 1,
    "not_provided|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome": 1,
    "Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome|Neurodevelopmental_abnormality|Abnormal_facial_shape|Abnormality_of_blood_and_blood-forming_tissues|Abnormality_of_the_immune_system|Postnatal_growth_retardation|not_provided|Noonan-like_syndrome": 1,
    "not_specified|not_provided|Macrothrombocytopenia-lymphedema-developmental_delay-facial_dysmorphism-camptodactyly_syndrome": 1,
    "not_provided|CDC42-associated_inflammatory_disease": 1,
    "WNT4-related_disorder": 5,
    "Inborn_genetic_diseases|Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome": 2,
    "Inborn_genetic_diseases|Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome|not_provided": 1,
    "not_provided|Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome": 2,
    "SERKAL_syndrome|Mullerian_aplasia_and_hyperandrogenism|Mayer-Rokitansky-Kuster-Hauser_syndrome": 1,
    "Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome": 27,
    "not_provided|SERKAL_syndrome|Mullerian_aplasia_and_hyperandrogenism": 3,
    "SERKAL_syndrome|Mullerian_aplasia_and_hyperandrogenism|not_provided": 4,
    "SERKAL_syndrome": 2,
    "not_specified|not_provided|Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome": 1,
    "WNT4-related_disorder|not_provided": 3,
    "Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome|not_provided": 2,
    "Mullerian_aplasia_and_hyperandrogenism|SERKAL_syndrome|WNT4-related_disorder": 1,
    "Mullerian_aplasia_and_hyperandrogenism": 4,
    "SERKAL_syndrome|Mullerian_aplasia_and_hyperandrogenism": 1,
    "ZBTB40-related_disorder|not_provided": 1,
    "ZBTB40-related_disorder": 8,
    "C1Q_deficiency|not_provided": 7,
    "C1Q_deficiency|C1QA-related_disorder|not_provided": 1,
    "not_provided|C1Q_deficiency": 2,
    "C1Q_deficiency_1": 1,
    "C1QA-related_disorder": 1,
    "C1Q_deficiency": 5,
    "C1Q_deficiency|not_provided|not_specified": 1,
    "C1Q_deficiency_1|C1Q_deficiency|not_provided": 1,
    "C1QC-related_disorder|not_provided": 2,
    "not_provided|C1Q_deficiency_3": 2,
    "not_provided|C1QC-related_disorder": 1,
    "C1Q_deficiency|C1Q_deficiency_3|not_provided": 1,
    "not_provided|C1Q_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|C1Q_deficiency": 1,
    "Inborn_genetic_diseases|C1Q_deficiency": 1,
    "C1Q_deficiency_2": 21,
    "C1Q_deficiency_2|not_provided": 3,
    "not_provided|C1QB-related_disorder": 3,
    "C1Q_deficiency_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|C1Q_deficiency_2": 1,
    "Inborn_genetic_diseases|C1Q_deficiency_2": 3,
    "C1Q_deficiency|C1Q_deficiency_2|not_provided": 1,
    "C1Q_deficiency|Inborn_genetic_diseases": 1,
    "C1QB-related_disorder": 1,
    "not_provided|C1Q_deficiency_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|C1Q_deficiency_2|not_provided": 1,
    "Cystic_fibrosis": 3250,
    "C1QB-related_disorder|not_provided": 2,
    "EPHB2-related_disorder": 14,
    "not_provided|EPHB2-related_disorder": 4,
    "Irido-corneo-trabecular_dysgenesis": 9,
    "Prostate_cancer/brain_cancer_susceptibility|not_provided": 1,
    "not_specified|not_provided|EPHB2-related_disorder": 1,
    "EPHB2-related_disorder|not_provided": 1,
    "Prostate_cancer/brain_cancer_susceptibility|EPHB2-related_disorder|not_provided": 1,
    "Prostate_cancer/brain_cancer_susceptibility": 2,
    "Bleeding_disorder|_platelet-type|_22": 3,
    "Prostate_cancer/brain_cancer_susceptibility|Bleeding_disorder|_platelet-type|_22": 1,
    "Inborn_genetic_diseases|Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome": 5,
    "Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome|not_provided|KDM1A-related_disorder|not_specified": 1,
    "not_provided|KDM1A-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome": 1,
    "not_provided|Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome": 2,
    "KDM1A-related_disorder": 6,
    "not_provided|Inborn_genetic_diseases|Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome": 1,
    "ACTH-independent_macronodular_adrenal_hyperplasia_3": 4,
    "Inborn_genetic_diseases|KDM1A-related_disorder": 2,
    "Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome": 16,
    "Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|KDM1A-related_disorder": 1,
    "KDM1A-related_disorder|not_provided|Inborn_genetic_diseases": 4,
    "Neurodevelopmental_and_congenital_anomalies|not_provided": 1,
    "Congenital_ocular_coloboma|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KDM1A-related_disorder|not_provided": 1,
    "not_provided|KDM1A-related_disorder|Inborn_genetic_diseases": 1,
    "Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome|not_provided": 1,
    "KDM1A-related_disorder|not_provided": 1,
    "Intellectual_disability|Inborn_genetic_diseases": 31,
    "Inborn_genetic_diseases|not_provided|See_cases": 9,
    "not_provided|Inborn_genetic_diseases|KDM1A-related_disorder": 1,
    "KDM1A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|KDM1A-related_disorder|not_specified|Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome": 1,
    "Palatal_anomalies-widely_spaced_teeth-facial_dysmorphism-developmental_delay_syndrome|Inborn_genetic_diseases": 2,
    "HNRNPR-related_disorder": 2,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_skeletal_and_brain_abnormalities": 6,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_skeletal_and_brain_abnormalities|Inborn_genetic_diseases": 1,
    "not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_7": 5,
    "Diamond-Blackfan_anemia_7": 21,
    "RPL11-related_disorder": 4,
    "Diamond-Blackfan_anemia": 679,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_7": 8,
    "not_provided|Diamond-Blackfan_anemia_7|Diamond-Blackfan_anemia": 2,
    "Diamond-Blackfan_anemia|not_specified": 12,
    "not_specified|Diamond-Blackfan_anemia": 7,
    "Diamond-Blackfan_anemia|not_provided": 19,
    "Diamond-Blackfan_anemia_7|Diamond-Blackfan_anemia": 17,
    "Diamond-Blackfan_anemia|RPL11-related_disorder": 1,
    "RPL11-related_disorder|not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_7": 1,
    "Diamond-Blackfan_anemia_7|not_provided": 1,
    "Anemia|Reticulocytopenia": 1,
    "not_specified|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_7": 1,
    "not_provided|Diamond-Blackfan_anemia_7": 1,
    "UDPglucose-4-epimerase_deficiency": 290,
    "GALE-related_disorder|UDPglucose-4-epimerase_deficiency": 6,
    "UDPglucose-4-epimerase_deficiency|GALE-related_disorder": 1,
    "UDPglucose-4-epimerase_deficiency|not_provided": 10,
    "UDPglucose-4-epimerase_deficiency|Thrombocytopenia_13|_syndromic": 16,
    "not_provided|UDPglucose-4-epimerase_deficiency": 9,
    "GALE-related_disorder|not_provided|UDPglucose-4-epimerase_deficiency": 1,
    "not_specified|not_provided|UDPglucose-4-epimerase_deficiency": 4,
    "not_specified|UDPglucose-4-epimerase_deficiency": 1,
    "UDPglucose-4-epimerase_deficiency|not_specified": 1,
    "not_provided|UDPglucose-4-epimerase_deficiency|not_specified": 1,
    "UDPglucose-4-epimerase_deficiency|Inborn_genetic_diseases": 3,
    "UDPglucose-4-epimerase_deficiency|Thrombocytopenia_13|_syndromic|not_provided": 1,
    "GALE-related_disorder": 2,
    "UDPglucose-4-epimerase_deficiency|GALE-related_disorder|not_provided|not_specified": 1,
    "GALE-related_disorder|not_specified|not_provided|UDPglucose-4-epimerase_deficiency": 1,
    "Thrombocytopenia_13|_syndromic|not_provided|UDPglucose-4-epimerase_deficiency|not_specified": 1,
    "not_specified|UDPglucose-4-epimerase_deficiency|Thrombocytopenia_13|_syndromic": 1,
    "UDPglucose-4-epimerase_deficiency|Thrombocytopenia_13|_syndromic|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|UDPglucose-4-epimerase_deficiency|not_specified": 1,
    "Thrombocytopenia_13|_syndromic|UDPglucose-4-epimerase_deficiency|not_provided|See_cases": 1,
    "UDPglucose-4-epimerase_deficiency|not_specified|not_provided": 1,
    "UDPglucose-4-epimerase_deficiency|Thrombocytopenia_13|_syndromic|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|UDPglucose-4-epimerase_deficiency": 1,
    "Thrombocytopenia_13|_syndromic|UDPglucose-4-epimerase_deficiency": 1,
    "Inborn_genetic_diseases|UDPglucose-4-epimerase_deficiency|Galactosemia_III|_severe|not_provided|Thrombocytopenia_13|_syndromic": 1,
    "Thrombocytopenia_13|_syndromic": 1,
    "Thrombocytopenia_13|_syndromic|UDPglucose-4-epimerase_deficiency|not_provided": 1,
    "Thrombocytopenia_13|_syndromic|UDPglucose-4-epimerase_deficiency|not_provided|not_specified": 1,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_provided|UDPglucose-4-epimerase_deficiency": 2,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 388,
    "not_provided|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 15,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_provided": 7,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Inborn_genetic_diseases|not_provided": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 116,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|HMGCL-related_disorder": 7,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 7,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_specified": 3,
    "not_specified|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 4,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 10,
    "Inborn_genetic_diseases|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 5,
    "HMGCL-related_disorder|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "HMGCL-related_disorder|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_specified": 1,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Inborn_genetic_diseases": 4,
    "HMGCL-related_disorder": 2,
    "not_provided|HMGCL-related_disorder|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 2,
    "not_specified|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|HMGCL-related_disorder": 1,
    "not_provided|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|not_specified|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 2,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|HMGCL-related_disorder": 1,
    "Inborn_genetic_diseases|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_provided": 1,
    "HMGCL-related_disorder|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_provided": 1,
    "not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "not_provided|Inborn_genetic_diseases|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "not_specified|HMGCL-related_disorder|Deficiency_of_hydroxymethylglutaryl-CoA_lyase": 1,
    "not_provided|Deficiency_of_hydroxymethylglutaryl-CoA_lyase|not_specified": 1,
    "Deficiency_of_hydroxymethylglutaryl-CoA_lyase|Inborn_genetic_diseases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Fucosidosis": 345,
    "Fucosidosis|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|Fucosidosis": 10,
    "Fucosidosis|Intellectual_disability": 1,
    "not_provided|Fucosidosis": 9,
    "Fucosidosis|FUCA1-related_disorder|not_provided": 1,
    "not_provided|FUCA1-related_disorder|Fucosidosis": 2,
    "Fucosidosis|not_provided": 8,
    "FUCA1-related_disorder|not_provided|not_specified|Fucosidosis": 1,
    "Fucosidosis|not_provided|FUCA1-related_disorder": 2,
    "not_specified|Fucosidosis|not_provided": 3,
    "Inborn_genetic_diseases|Fucosidosis|not_provided": 1,
    "FU1/FU2_POLYMORPHISM|Fucosidosis|not_provided": 1,
    "FUCA1-related_disorder|not_provided|Fucosidosis": 1,
    "Fucosidosis|Abnormality_of_the_nervous_system": 1,
    "FUCA1-related_disorder|Fucosidosis": 2,
    "Inborn_genetic_diseases|not_provided|Fucosidosis": 1,
    "not_specified|Fucosidosis": 1,
    "FUCA1-related_disorder|not_provided|Fucosidosis|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Fucosidosis": 1,
    "Fucosidosis|Intellectual_disability|FUCA1-related_disorder|not_provided": 1,
    "Fucosidosis|not_specified": 1,
    "Fucosidosis|FUCA1-related_disorder|not_provided|not_specified": 1,
    "Fucosidosis|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|FUCA1-related_disorder": 1,
    "not_specified|not_provided|Fucosidosis": 2,
    "not_provided|not_specified|Fucosidosis": 1,
    "not_specified|Flexion_contracture|not_provided": 1,
    "IFNLR1-related_disorder": 12,
    "IFNLR1-related_disorder|not_specified": 1,
    "not_provided|IFNLR1-related_disorder": 2,
    "not_specified|IFNLR1-related_disorder": 1,
    "IFNLR1-related_disorder|not_provided": 1,
    "Van_der_Woude_syndrome_2": 50,
    "Isolated_cleft_palate": 6,
    "Isolated_cleft_palate|GRHL3-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|GRHL3-related_disorder": 1,
    "GRHL3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Van_der_Woude_syndrome_2|not_specified": 1,
    "GRHL3-related_disorder": 19,
    "Van_der_Woude_syndrome_2|GRHL3-related_disorder": 3,
    "Van_der_Woude_syndrome_2|not_provided|GRHL3-related_disorder": 2,
    "not_provided|Van_der_Woude_syndrome_2|GRHL3-related_disorder": 2,
    "GRHL3-related_disorder|not_provided|Van_der_Woude_syndrome_2": 2,
    "not_provided|Van_der_Woude_syndrome_2": 6,
    "not_provided|Isolated_cleft_palate|Van_der_Woude_syndrome_2": 1,
    "not_provided|GRHL3-related_disorder": 1,
    "GRHL3-related_disorder|Van_der_Woude_syndrome_2": 1,
    "Van_der_Woude_syndrome_2|Inborn_genetic_diseases": 1,
    "Van_der_Woude_syndrome_2|Isolated_cleft_palate|not_provided": 1,
    "Inborn_genetic_diseases|Van_der_Woude_syndrome_2": 1,
    "Van_der_Woude_syndrome_2|GRHL3-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Van_der_Woude_syndrome_1": 1,
    "Van_der_Woude_syndrome": 2,
    "Van_der_Woude_syndrome_2|not_provided": 3,
    "GRHL3-related_disorder|not_specified|not_provided|Van_der_Woude_syndrome_2": 1,
    "NIPAL3-related_disorder": 9,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_14": 4,
    "Weakened_expression_of_D_antigen": 1,
    "weakened_D_expression_by_serology": 3,
    "Hemolytic_disease_of_fetus_and_newborn|_RH-induced|RhD_category_D-VII": 1,
    "Blood_group_antigen_abnormality": 1,
    "serologic_weak_D_phenotype": 1,
    "not_provided|Rhd|_weak_d|_type_I": 1,
    "Anti-D_isoimmunization_affecting_pregnancy|Hemolytic_disease_of_fetus_OR_newborn_due_to_RhD_isoimmunization": 1,
    "RhD_negative": 1,
    "RH-NULL|_AMORPH_TYPE": 4,
    "altered_RhC_expression": 1,
    "RH_E/e_POLYMORPHISM": 1,
    "Hypercholesterolemia|_familial|_4": 319,
    "not_provided|Hypercholesterolemia|_familial|_4": 6,
    "LDLRAP1-related_disorder": 1,
    "Familial_hypercholesterolemia": 1210,
    "Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype": 21,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4": 37,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4|Familial_hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4": 15,
    "Hypercholesterolemia|_familial|_4|LDLRAP1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4": 7,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4": 1,
    "Hypercholesterolemia|_familial|_4|not_specified|Cardiovascular_phenotype": 2,
    "not_specified|Hypercholesterolemia|_familial|_4": 3,
    "Hypercholesterolemia|_familial|_4|Familial_hypercholesterolemia": 2,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified": 222,
    "Hypercholesterolemia|_familial|_4|not_specified": 7,
    "Hypercholesterolemia|_familial|_4|not_provided": 4,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_4": 3,
    "not_specified|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "LDLRAP1-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4": 2,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 9,
    "not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4": 2,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype": 43,
    "not_provided|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_familial|_4": 6,
    "Cardiovascular_phenotype|not_specified|LDLRAP1-related_disorder|Hypercholesterolemia|_familial|_4|not_provided": 1,
    "not_specified|Cardiovascular_phenotype": 216,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_familial|_4": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_4": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4|LDLRAP1-related_disorder": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_familial|_4": 1,
    "Hypercholesterolemia|_familial|_4|See_cases": 1,
    "Cardiovascular_phenotype|not_provided": 2637,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4|not_provided": 2,
    "not_provided|Cardiovascular_phenotype": 2490,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_4": 3,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4|not_specified": 1,
    "Hypercholesterolemia|_familial|_4|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4|not_provided": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia": 86,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypercholesterolemia|_familial|_4": 1,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_4": 1,
    "Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_4": 2,
    "Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_4|Autosomal_recessive_inheritance": 1,
    "not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4|not_provided": 1,
    "LDLRAP1-related_disorder|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_4": 1,
    "Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype|not_specified": 2,
    "Hypercholesterolemia|_familial|_4|LDLRAP1-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|not_provided|Hypercholesterolemia|_familial|_4": 1,
    "not_specified|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4|not_provided|not_specified": 1,
    "not_specified|not_provided|Hypercholesterolemia|_familial|_4|Cardiovascular_phenotype": 1,
    "not_specified|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_4": 1,
    "Hypercholesterolemia|_familial|_1": 1395,
    "not_provided|MAN1C1-related_disorder": 1,
    "not_specified|MAN1C1-related_disorder": 1,
    "MAN1C1-related_disorder": 7,
    "Eichsfeld_type_congenital_muscular_dystrophy": 371,
    "SEPN1-related_disorder|not_specified|not_provided": 1,
    "not_specified|SEPN1-related_disorder": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 3,
    "not_provided|SELENON-related_disorder|SEPN1-related_disorder": 1,
    "SEPN1-related_disorder": 57,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 21,
    "Inborn_genetic_diseases|not_provided|Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|not_specified": 7,
    "Eichsfeld_type_congenital_muscular_dystrophy|Inborn_genetic_diseases": 20,
    "Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|not_specified|not_provided": 2,
    "Eichsfeld_type_congenital_muscular_dystrophy|not_provided|Inborn_genetic_diseases": 2,
    "Eichsfeld_type_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Eichsfeld_type_congenital_muscular_dystrophy": 15,
    "Inborn_genetic_diseases|SEPN1-related_disorder|not_specified|not_provided|Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|not_provided": 16,
    "Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder": 4,
    "not_specified|Eichsfeld_type_congenital_muscular_dystrophy": 6,
    "Inborn_genetic_diseases|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 6,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|not_specified": 1,
    "SEPN1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Eichsfeld_type_congenital_muscular_dystrophy|not_specified|not_provided": 1,
    "SEPN1-related_disorder|not_specified|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 4,
    "Eichsfeld_type_congenital_muscular_dystrophy|not_specified|not_provided": 3,
    "not_provided|SEPN1-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 2,
    "Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Eichsfeld_type_congenital_muscular_dystrophy": 2,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy|not_specified": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|Joint_laxity|EMG_abnormality|EMG:_myopathic_abnormalities|Pain|See_cases|not_provided": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|See_cases": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|SELENON-related_disorder|not_provided": 1,
    "SELENON-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Eichsfeld_type_congenital_muscular_dystrophy|not_provided": 1,
    "SEPN1-related_disorder|Inborn_genetic_diseases|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "SELENON-related_disorder|SEPN1-related_disorder|not_provided|Eichsfeld_type_congenital_muscular_dystrophy|not_specified": 1,
    "SEPN1-related_disorder|not_specified|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "SELENON-related_myopathy|Muscular_dystrophy|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "not_provided|Congenital_myopathy_4A|_autosomal_dominant|Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_4A|_autosomal_dominant": 9,
    "not_specified|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 4,
    "not_provided|SELENON-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion|not_provided|See_cases": 1,
    "Congenital_myopathy_4A|_autosomal_dominant|Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|SELENON-related_myopathy|not_provided|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|not_specified|SEPN1-related_disorder|not_provided": 1,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Eichsfeld_type_congenital_muscular_dystrophy|not_provided": 1,
    "SELENON-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "SEPN1-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 2,
    "not_provided|Congenital_myopathy_4A|_autosomal_dominant": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Eichsfeld_type_congenital_muscular_dystrophy|See_cases|not_provided": 1,
    "SELENON-related_disorder": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|SELENON-related_disorder": 1,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|SELENON-related_disorder": 1,
    "not_provided|not_specified|SEPN1-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "SEPN1-related_disorder|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|SELENON-related_disorder|not_provided": 1,
    "not_provided|SEPN1-related_disorder|Inborn_genetic_diseases|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy|See_cases": 1,
    "not_specified|Eichsfeld_type_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|SEPN1-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "SEPN1-related_disorder|Muscular_dystrophy|Cleft_lip/palate|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "not_specified|Eichsfeld_type_congenital_muscular_dystrophy|not_provided": 1,
    "Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder|not_provided|not_specified": 1,
    "Congenital_myopathy_4A|_autosomal_dominant|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "not_specified|SELENON-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "SEPN1-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy|not_provided": 1,
    "SELENON-related_disorder|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "not_specified|Eichsfeld_type_congenital_muscular_dystrophy|SEPN1-related_disorder": 3,
    "not_provided|Eichsfeld_type_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Eichsfeld_type_congenital_muscular_dystrophy|not_provided|SEPN1-related_disorder|not_specified": 1,
    "SEPN1-related_disorder|not_specified|not_provided|Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "SELENON-related_disorder|Eichsfeld_type_congenital_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided": 1,
    "not_specified|SEPN1-related_disorder|not_provided|Eichsfeld_type_congenital_muscular_dystrophy": 1,
    "not_provided|SEPN1-related_disorder|not_specified": 1,
    "SEPN1-related_disorder|not_provided": 5,
    "not_provided|SEPN1-related_disorder": 4,
    "Zinc_deficiency|_transient_neonatal": 6,
    "SLC30A2-related_disorder": 3,
    "Hypertrophic_cardiomyopathy": 5066,
    "not_provided|not_specified|TRIM63-related_disorder": 2,
    "Hypertrophic_cardiomyopathy|Inborn_genetic_diseases": 1,
    "CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31": 1,
    "TRIM63-related_disorder": 3,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy": 28,
    "Inborn_genetic_diseases|Hypertrophic_cardiomyopathy": 2,
    "CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31|Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Inborn_genetic_diseases": 7,
    "Primary_familial_hypertrophic_cardiomyopathy": 273,
    "not_provided|TRIM63-related_disorder|not_specified": 1,
    "See_cases|CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31|Inborn_genetic_diseases|Hypertrophic_cardiomyopathy": 1,
    "not_provided|CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31": 1,
    "Cardiovascular_phenotype|CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31": 1,
    "not_specified|Hypertrophic_cardiomyopathy": 319,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|Hypertrophic_cardiomyopathy": 1,
    "Idiopathic_cardiomyopathy": 2,
    "CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31|Cardiovascular_phenotype|not_specified|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "TRIM63-related_disorder|Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|TRIM63-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|CARDIOMYOPATHY|_FAMILIAL_HYPERTROPHIC|_31": 1,
    "Usher_syndrome_type_2C|not_specified|not_provided": 16,
    "CNKSR1-related_disorder": 1,
    "CNKSR1-related_disorder|not_provided": 1,
    "CD52-related_disorder": 3,
    "not_provided|Retinitis_pigmentosa": 501,
    "Retinitis_pigmentosa_59": 396,
    "DHDDS-related_disorder|Retinitis_pigmentosa_59": 4,
    "Retinitis_pigmentosa_59|Retinitis_pigmentosa": 4,
    "Retinitis_pigmentosa_59|DHDDS-related_disorder": 1,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities": 6,
    "Retinitis_pigmentosa_59|Inborn_genetic_diseases": 12,
    "not_provided|Retinitis_pigmentosa_59|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_59|not_provided": 5,
    "Retinitis_pigmentosa_59|Developmental_delay_and_seizures_with_or_without_movement_abnormalities|not_provided": 1,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities|not_provided|Retinitis_pigmentosa_59": 2,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities|Retinitis_pigmentosa_59|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_delay_and_seizures_with_or_without_movement_abnormalities": 1,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities|Retinitis_pigmentosa_59|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_59|Developmental_delay_and_seizures_with_or_without_movement_abnormalities": 2,
    "Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_59": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Retinitis_pigmentosa_59": 1,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities|Retinitis_pigmentosa_59": 6,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_59": 9,
    "not_provided|Retinitis_pigmentosa_59": 9,
    "Congenital_disorder_of_glycosylation|_type_Ibb": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_59|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_59|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities|Retinitis_pigmentosa_59|Retinitis_pigmentosa|Retinal_dystrophy|not_specified": 1,
    "Developmental_delay_and_seizures_with_or_without_movement_abnormalities|Retinitis_pigmentosa_59|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_59|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|DHDDS-related_disorder|Retinitis_pigmentosa_59|Retinal_dystrophy": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_59": 1,
    "Retinitis_pigmentosa_59|Congenital_disorder_of_glycosylation|_type_Ibb": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_59": 4,
    "not_specified|not_provided|Retinitis_pigmentosa_59|DHDDS-related_disorder": 1,
    "Retinitis_pigmentosa_59|not_specified": 1,
    "Retinitis_pigmentosa_59|Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "DHDDS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_59": 1,
    "not_specified|Retinitis_pigmentosa_59|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_59|Retinal_dystrophy|Developmental_delay_and_seizures_with_or_without_movement_abnormalities": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa_59|See_cases": 1,
    "Retinitis_pigmentosa_59|Developmental_delay_and_seizures_with_or_without_movement_abnormalities|not_specified": 1,
    "Retinitis_pigmentosa_59|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_59|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_59|Inborn_genetic_diseases|not_specified|Retinal_dystrophy|not_provided|DHDDS-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_59": 1,
    "DHDDS-CDG": 1,
    "Retinitis_Pigmentosa|_Recessive": 86,
    "not_provided|Intellectual_disability|_autosomal_dominant_14|Coffin-Siris_syndrome_1": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_14": 24,
    "not_provided|ARID1A-related_disorder": 23,
    "Inborn_genetic_diseases|Astrocytoma|ARID1A-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|ARID1A-related_disorder": 1,
    "ARID1A-related_disorder|not_provided": 29,
    "ARID1A-related_disorder": 47,
    "Intellectual_disability|_autosomal_dominant_14": 114,
    "Intellectual_disability|_autosomal_dominant_14|not_specified|not_provided": 4,
    "not_provided|Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_14": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_dominant_14": 4,
    "ARID1A-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_14": 4,
    "ARID1A-related_BAFopathy|Intellectual_disability|_autosomal_dominant_14": 2,
    "not_specified|not_provided|ARID1A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Coffin-Siris_syndrome": 2,
    "ARID1A-related_disorder|not_specified|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_14|not_provided": 19,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_14": 6,
    "Intellectual_disability|_autosomal_dominant_14|not_provided|not_specified": 1,
    "not_provided|Coffin-Siris_syndrome_1": 40,
    "ARID1A-related_disorder|Intellectual_disability|_autosomal_dominant_14|not_provided": 1,
    "not_provided|not_specified|Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_14": 1,
    "not_provided|ARID1A-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_14": 1,
    "Malignant_tumor_of_urinary_bladder": 104,
    "Intellectual_disability|_autosomal_dominant_14|Intellectual_disability|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_14|ARID1A-related_disorder": 2,
    "Primary_low_grade_serous_adenocarcinoma_of_ovary": 1,
    "not_specified|ARID1A-related_disorder|not_provided": 1,
    "not_provided|Coffin-Siris_syndrome": 7,
    "Intellectual_disability|_autosomal_dominant_14|ARID1A-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_14|ARID1A-related_BAFopathy": 2,
    "not_provided|ARID1A-related_disorder|Inborn_genetic_diseases": 1,
    "Colorectal_cancer": 286,
    "ARID1A-related_BAFopathy": 3,
    "ARID1A-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_14": 2,
    "not_specified|Intellectual_disability|_autosomal_dominant_14|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Skeletal_dysplasia": 1,
    "ARID1A-related_BAFopathy|not_specified|Intellectual_disability|_autosomal_dominant_14": 1,
    "Coffin-Siris_syndrome_1|ARID1A-related_BAFopathy|Intellectual_disability|_autosomal_dominant_14": 1,
    "Clonal_Cytopenia_of_Undetermined_Significance": 1,
    "Medulloblastoma": 84,
    "Coffin-Siris_syndrome_1|Intellectual_disability|_autosomal_dominant_14|not_provided": 1,
    "Coffin-Siris_syndrome": 32,
    "Inborn_genetic_diseases|ARID1A-related_disorder|not_provided": 1,
    "Coffin-Siris_syndrome_1": 257,
    "Intellectual_disability|_autosomal_dominant_14|ARID1A-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|ARID1A-related_disorder": 1,
    "Coffin-Siris_syndrome_1|Intellectual_disability|_autosomal_dominant_14": 1,
    "Neurodevelopmental_delay|not_provided": 6,
    "AKT1_Inhibitor_response": 1,
    "Intellectual_disability|_autosomal_dominant_14|Marfanoid_habitus_and_intellectual_disability|not_provided": 1,
    "not_provided|ARID1A-related_disorder|Intellectual_disability|_autosomal_dominant_14": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_14|Intellectual_disability": 1,
    "ARID1A-related_disorder|not_provided|not_specified|Intellectual_disability|_autosomal_dominant_14": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_14|Congenital_cerebellar_hypoplasia|Severe_global_developmental_delay|Periventricular_leukomalacia|Seizure|Absent_speech|Microcephaly": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_14|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Coffin-Siris_syndrome": 4,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_14|Malignant_tumor_of_urinary_bladder": 1,
    "Inborn_genetic_diseases|ARID1A-related_disorder": 1,
    "Intellectual_disability|not_provided|ARID1A-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_14": 2,
    "not_specified|ARID1A-related_disorder": 1,
    "not_provided|ARID1A-related_disorder|not_specified": 1,
    "not_provided|Intellectual_disability|Intellectual_disability|_autosomal_dominant_14|Inborn_genetic_diseases": 1,
    "Hepatoblastoma": 16,
    "Endometrial_carcinoma": 113,
    "ARID1A-related_BAFopathy|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_14|ARID1A-related_disorder|not_provided": 1,
    "Septo-optic_dysplasia_sequence": 8,
    "Obesity|not_provided|Inborn_genetic_diseases": 2,
    "Hyperphosphatasia-intellectual_disability_syndrome|not_provided": 1,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_1": 8,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|not_provided": 9,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1": 33,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_1|PIGV-related_disorder|not_specified": 2,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|not_provided|PIGV-related_disorder": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_1|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_1|not_provided": 2,
    "not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_1|PIGV-related_disorder|not_provided": 1,
    "PIGV-related_disorder|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_1": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_1": 1,
    "PIGV-related_disorder|not_provided": 1,
    "PIGV-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_1|PIGV-related_disorder": 1,
    "PIGV-related_disorder": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|not_provided|PIGV-related_disorder|Inborn_genetic_diseases|Hyperphosphatasia-intellectual_disability_syndrome": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_1|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Elevated_circulating_alkaline_phosphatase_concentration|not_provided": 1,
    "Hyperphosphatasia-intellectual_disability_syndrome": 3,
    "Perrault_syndrome_1": 21,
    "GPATCH3-related_disorder": 6,
    "NR0B2-related_disorder": 58,
    "NR0B2-related_disorder|Inherited_obesity|not_provided": 1,
    "NR0B2-related_disorder|not_specified": 8,
    "Obesity|NR0B2-related_disorder|Inherited_obesity|not_specified": 1,
    "not_provided|NR0B2-related_disorder": 5,
    "NR0B2-related_disorder|Inherited_obesity": 1,
    "Inherited_obesity": 20,
    "NR0B2-related_disorder|not_provided": 6,
    "Obesity|_mild|_early-onset|not_specified": 1,
    "Obesity": 55,
    "Obesity|not_specified|not_provided": 2,
    "NR0B2-related_disorder|not_specified|not_provided": 1,
    "NR0B2-related_disorder|not_provided|not_specified": 1,
    "APC-mutation_negative_familial_colorectal_cancer|Obesity": 2,
    "Inherited_obesity|NR0B2-related_disorder": 1,
    "not_specified|NR0B2-related_disorder": 1,
    "Inherited_obesity|NR0B2-related_disorder|not_specified": 1,
    "not_specified|not_provided|NR0B2-related_disorder": 1,
    "Inherited_obesity|APC-mutation_negative_familial_colorectal_cancer|not_specified|NR0B2-related_disorder|not_provided": 1,
    "Obesity|_mild|_early-onset": 1,
    "NUDC-related_condition": 1,
    "not_provided|KDF1-related_disorder": 4,
    "KDF1-related_disorder|not_provided": 2,
    "Hypodontia": 53,
    "KDF1-related_disorder": 3,
    "Ectodermal_dysplasia_12|_hypohidrotic/hair/tooth/nail_type": 1,
    "Ectodermal_dysplasia_12|_hypohidrotic/hair/tooth/nail_type|KDF1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Ectodermal_dysplasia_12|_hypohidrotic/hair/tooth/nail_type|not_provided": 1,
    "not_provided|Ectodermal_dysplasia_12|_hypohidrotic/hair/tooth/nail_type": 1,
    "not_provided|Lichtenstein-Knorr_syndrome": 2,
    "SLC9A1-related_disorder|not_provided": 6,
    "Lichtenstein-Knorr_syndrome|not_provided": 3,
    "not_provided|SLC9A1-related_disorder": 3,
    "not_specified|SLC9A1-related_disorder": 1,
    "SLC9A1-related_disorder": 2,
    "not_provided|Lichtenstein-Knorr_syndrome|not_specified": 2,
    "Lichtenstein-Knorr_syndrome": 4,
    "Lichtenstein-Knorr_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_motor_and_speech_delay_and_behavioral_abnormalities": 1,
    "Neurodevelopmental_disorder_with_motor_and_speech_delay_and_behavioral_abnormalities": 6,
    "TMEM222-related_disorder": 1,
    "MAP3K6-related_disorder|not_provided": 7,
    "MAP3K6-related_disorder": 16,
    "not_provided|MAP3K6-related_disorder": 4,
    "MAP3K6-related_disorder|not_specified|not_provided": 1,
    "MAP3K6-related_disorder|not_provided|not_specified": 1,
    "not_specified|MAP3K6-related_disorder": 1,
    "Immunodeficiency_due_to_ficolin3_deficiency": 4,
    "not_provided|Immunodeficiency_due_to_ficolin3_deficiency": 1,
    "Rheumatic_heart_disease": 2,
    "Immunodeficiency_due_to_ficolin3_deficiency|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency_due_to_ficolin3_deficiency": 2,
    "FCN3-related_disorder|not_specified|not_provided": 1,
    "FCN3-related_disorder": 4,
    "not_specified|Microcephaly": 5,
    "not_provided|FCN3-related_disorder": 1,
    "not_specified|Immunodeficiency_due_to_ficolin3_deficiency": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided": 29,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 109,
    "not_provided|Inborn_genetic_diseases|Spastic_ataxia": 1,
    "AHDC1-related_disorder|not_provided": 14,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided|AHDC1-related_disorder": 4,
    "not_provided|AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 2,
    "AHDC1-related_disorder|not_provided|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 6,
    "AHDC1-related_disorder": 20,
    "not_provided|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 23,
    "Inborn_genetic_diseases|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 6,
    "AHDC1-related_disorder|Inborn_genetic_diseases|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided": 3,
    "AHDC1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided": 7,
    "not_provided|AHDC1-related_disorder": 15,
    "not_provided|Inborn_genetic_diseases|AHDC1-related_disorder": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_specified|AHDC1-related_disorder|not_provided": 1,
    "AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 3,
    "Inborn_genetic_diseases|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided": 5,
    "not_provided|Intellectual_disability|Inborn_genetic_diseases": 13,
    "not_provided|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|AHDC1-related_disorder": 3,
    "AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided|not_specified": 2,
    "AHDC1-related_disorder|not_provided|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|AHDC1-related_disorder": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|AHDC1-related_disorder|not_provided": 2,
    "Delayed_speech_and_language_development|Sleep_apnea|Hypotonia|Neonatal_hypotonia|Global_developmental_delay|Intellectual_disability|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 2,
    "Inborn_genetic_diseases|AHDC1-related_disorder": 1,
    "Abdominal_obesity-metabolic_syndrome_3|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided": 1,
    "AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|AHDC1-related_disorder": 1,
    "Neonatal_hypotonia|Delayed_speech_and_language_development|Global_developmental_delay|Intellectual_disability|Sleep_apnea|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Hypotonia|not_provided": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided|Intellectual_disability": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Inborn_genetic_diseases": 3,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Neurodevelopmental_abnormality|not_provided": 1,
    "Inborn_genetic_diseases|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_provided|AHDC1-related_disorder": 1,
    "not_specified|AHDC1-related_disorder|not_provided": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Cerebral_visual_impairment_and_intellectual_disability": 1,
    "not_specified|AHDC1-related_disorder|not_provided|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 1,
    "Neurodevelopmental_abnormality|not_provided": 8,
    "not_provided|AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 1,
    "AHDC1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|See_cases|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_specified": 1,
    "AHDC1-related_disorder|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome": 1,
    "Congenital_cerebellar_hypoplasia|AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|Cerebellar_vermis_hypoplasia": 1,
    "AHDC1-related_disorder|not_specified|not_provided": 1,
    "AHDC1-related_intellectual_disability_-_obstructive_sleep_apnea_-_mild_dysmorphism_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "XKR8-related_condition": 1,
    "not_specified|XKR8-related_condition": 1,
    "INFECTION-INDUCED_ACUTE-ONSET_AXONAL_NEUROPATHY|See_cases|not_specified": 2,
    "INFECTION-INDUCED_ACUTE-ONSET_AXONAL_NEUROPATHY|See_cases": 1,
    "INFECTION-INDUCED_ACUTE-ONSET_AXONAL_NEUROPATHY": 1,
    "Autism": 104,
    "Elliptocytosis_1": 63,
    "not_provided|Elliptocytosis_1|EPB41-related_disorder": 1,
    "EPB41-related_disorder|not_provided|Elliptocytosis_1": 1,
    "Elliptocytosis_1|not_provided": 12,
    "EPB41-related_disorder|not_provided": 1,
    "not_provided|Elliptocytosis_1": 14,
    "EPB41-related_disorder": 6,
    "Elliptocytosis_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Elliptocytosis_1|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Elliptocytosis_1": 1,
    "Hereditary_elliptocytosis": 1,
    "Inborn_genetic_diseases|Elliptocytosis_1": 2,
    "Elliptocytosis_1|EPB41-related_disorder": 2,
    "Elliptocytosis_1|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Elliptocytosis_1": 1,
    "EPB41-related_disorder|Elliptocytosis_1": 1,
    "Inborn_genetic_diseases|Elliptocytosis_1|not_provided|EPB41-related_disorder": 1,
    "Elliptocytosis_1|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Elliptocytosis_1|not_specified": 1,
    "not_provided|MECR-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities": 4,
    "Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities": 6,
    "Childhood_Onset_Dystonias|Optic_atrophy|not_provided|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities": 1,
    "Childhood_Onset_Dystonias|Optic_atrophy|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities": 1,
    "Optic_atrophy|Childhood_Onset_Dystonias|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities|not_provided|Mitochondrial_disease|Optic_atrophy_16": 1,
    "not_provided|MECR-related_disorder": 5,
    "Childhood_Onset_Dystonias|Optic_atrophy|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities|Optic_atrophy_16|not_provided": 1,
    "Childhood_Onset_Dystonias|Optic_atrophy|not_provided|MECR-related_disorder|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities|Mitochondrial_disease": 1,
    "Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities|not_provided": 1,
    "Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities|Optic_atrophy_16": 1,
    "MECR-related_disorder|not_provided": 2,
    "MECR-related_disorder": 1,
    "Optic_atrophy|Childhood_Onset_Dystonias|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities|not_provided": 1,
    "Optic_atrophy_16|Dystonia|_childhood-onset|_with_optic_atrophy_and_basal_ganglia_abnormalities": 1,
    "PTPRU-related_disorder": 24,
    "PTPRU-related_disorder|not_provided": 2,
    "Congenital_heart_defects_and_ectodermal_dysplasia": 26,
    "Obesity|_association_with": 2,
    "PUM1-associated_developmental_disability-ataxia-seizure_syndrome|Inborn_genetic_diseases|Spinocerebellar_ataxia_47|not_provided": 1,
    "PUM1-associated_developmental_disability-ataxia-seizure_syndrome|Spinocerebellar_ataxia_47": 2,
    "PUM1-related_disorder": 15,
    "not_provided|PUM1-related_disorder": 6,
    "Spinocerebellar_ataxia_47": 20,
    "Neurodevelopmental_disorder|not_provided": 44,
    "Spinocerebellar_ataxia_47|not_provided": 2,
    "not_provided|Spinocerebellar_ataxia_47": 5,
    "Spinocerebellar_ataxia_47|Late-onset_spinocerebellar_ataxia|not_provided": 1,
    "not_provided|PUM1-related_disorder|Inborn_genetic_diseases": 1,
    "PUM1-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia_47|Inborn_genetic_diseases": 2,
    "PUM1-associated_developmental_disability-ataxia-seizure_syndrome": 4,
    "PUM1-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|PUM1-related_disorder": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_47|PUM1-associated_developmental_disability-ataxia-seizure_syndrome": 1,
    "Spinocerebellar_ataxia_47|Global_developmental_delay|Seizure|Intellectual_disability": 1,
    "Spastic_ataxia": 31,
    "PUM1-associated_developmental_disability-ataxia-seizure_syndrome|Spinocerebellar_ataxia_47|not_specified": 1,
    "Progressive_spastic_paraparesis": 1,
    "Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 44,
    "Bardet-Biedl_syndrome_1": 152,
    "CCDC28B-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|_modifier_of": 1,
    "not_provided|Bardet-Biedl_syndrome_1": 10,
    "CCDC28B-related_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_LCK_deficiency": 242,
    "Severe_combined_immunodeficiency_due_to_LCK_deficiency|not_specified": 5,
    "not_provided|Severe_combined_immunodeficiency_due_to_LCK_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_LCK_deficiency|not_provided": 2,
    "not_provided|Severe_combined_immunodeficiency_due_to_LCK_deficiency": 3,
    "Severe_combined_immunodeficiency_disease": 49,
    "not_provided|Severe_combined_immunodeficiency_due_to_LCK_deficiency|LCK-related_disorder|not_specified": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_LCK_deficiency": 4,
    "Severe_combined_immunodeficiency_due_to_LCK_deficiency|LCK-related_disorder": 3,
    "not_provided|Severe_combined_immunodeficiency_due_to_LCK_deficiency|LCK-related_disorder": 1,
    "LCK-related_disorder|Severe_combined_immunodeficiency_due_to_LCK_deficiency": 3,
    "LCK-related_disorder": 1,
    "HDAC1-related_disorder|not_provided": 2,
    "HDAC1-related_disorder": 1,
    "SYNC-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C": 356,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 22,
    "Charcot-Marie-Tooth|_Intermediate": 3,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided": 18,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Inborn_genetic_diseases": 19,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 22,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 2,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C|Inborn_genetic_diseases": 4,
    "YARS1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C|Inborn_genetic_diseases": 1,
    "YARS1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "YARS1-related_disorder|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "YARS1-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 10,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "not_provided|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|recessive_ARS-related_multisystem_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided": 1,
    "YARS1-related_disorder|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 3,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_specified": 2,
    "YARS1-related_disorder": 2,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 2,
    "Metachromatic_leukodystrophy": 955,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided|Inborn_genetic_diseases|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|YARS1-related_disorder": 2,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Retinal_degeneration|Hepatic_steatosis|Severe_hearing_impairment|Primary_amenorrhea|Corpus_callosum|_agenesis_of": 1,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Global_developmental_delay|Cholestatic_liver_disease|Hyperinsulinemic_hypoglycemia|Anemia|Liver_failure|Acute_kidney_injury|Recurrent_infections": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_C|Inborn_genetic_diseases|YARS1-related_disorder": 1,
    "not_specified|Charcot-Marie-Tooth|_Intermediate|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_provided": 1,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset": 3,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Charcot-Marie-Tooth|_Intermediate|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Neurodevelopmental_delay": 1,
    "not_specified|YARS1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|Neurodevelopmental_delay": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|YARS1-related_disorder|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_C|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_C|not_specified|not_provided": 1,
    "HPCA-related_disorder|not_provided": 2,
    "Torsion_dystonia_2": 3,
    "HPCA-related_disorder": 1,
    "Torsion_dystonia_2|not_provided": 1,
    "Reticular_dysgenesis": 130,
    "AK2-related_disorder": 3,
    "Inborn_genetic_diseases|Reticular_dysgenesis": 5,
    "Reticular_dysgenesis|Inborn_genetic_diseases": 3,
    "Reticular_dysgenesis|AK2-related_disorder": 3,
    "Reticular_dysgenesis|not_provided": 5,
    "AK2-related_disorder|not_provided|Reticular_dysgenesis": 1,
    "not_specified|not_provided|Reticular_dysgenesis": 1,
    "AK2-related_disorder|not_provided|Reticular_dysgenesis|not_specified": 1,
    "Reticular_dysgenesis|AK2-related_disorder|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|Reticular_dysgenesis": 4,
    "not_specified|Reticular_dysgenesis": 1,
    "not_provided|Reticular_dysgenesis": 7,
    "AK2-related_disorder|Reticular_dysgenesis": 2,
    "not_provided|Reticular_dysgenesis|AK2-related_disorder": 2,
    "not_specified|AK2-related_disorder|Reticular_dysgenesis|not_provided": 1,
    "not_provided|AK2-related_disorder|Reticular_dysgenesis": 1,
    "Reticular_dysgenesis|not_provided|AK2-related_disorder": 1,
    "AK2-related_disorder|Reticular_dysgenesis|not_provided": 1,
    "not_specified|PHC2-related_disorder": 1,
    "Attention_deficit_hyperactivity_disorder": 10,
    "Erythrokeratodermia_variabilis_et_progressiva_2": 7,
    "Erythrokeratodermia_variabilis_et_progressiva_2|Inborn_genetic_diseases": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_2|not_provided": 3,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_2": 3,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 2,
    "not_provided|not_specified|Erythrokeratodermia_variabilis_et_progressiva_2": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|GJB4-related_disorder": 3,
    "not_provided|GJB4-related_disorder|Erythrokeratodermia_variabilis_et_progressiva_2": 1,
    "GJB4-related_disorder": 1,
    "GJB4-related_disorder|not_provided": 2,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_1|Erythrokeratodermia_variabilis_et_progressiva_2": 1,
    "GJB4-related_disorder|not_provided|not_specified": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_1": 40,
    "Erythrokeratodermia_variabilis_et_progressiva_1|not_provided": 9,
    "not_provided|not_specified|GJB3-related_disorder": 1,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_1": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A": 54,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_dominant_nonsyndromic_hearing_loss_2B": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "GJB3-related_disorder": 1,
    "not_specified|not_provided|Erythrokeratodermia_variabilis_et_progressiva_1": 3,
    "Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_dominant_nonsyndromic_hearing_loss_2B": 1,
    "not_provided|GJB3-related_disorder": 3,
    "not_specified|not_provided|GJB3-related_disorder": 1,
    "not_specified|not_provided|Deafness|_autosomal_dominant|_with_peripheral_neuropathy|Hearing_impairment": 1,
    "not_provided|GJB3-related_disorder|Erythrokeratodermia_variabilis_et_progressiva_1|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_2B|Erythrokeratodermia_variabilis_et_progressiva_1|not_provided": 2,
    "not_specified|Erythrokeratodermia_variabilis_et_progressiva_1|GJB3-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Erythrokeratodermia_variabilis_et_progressiva_1": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2B": 1,
    "GJB3-related_disorder|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2B|Erythrokeratodermia_variabilis_et_progressiva_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2B|Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Erythrokeratodermia_variabilis": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_2B|Erythrokeratodermia_variabilis_et_progressiva_1": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2B|Erythrokeratodermia_variabilis_et_progressiva_1|not_specified": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_1|not_provided|not_specified": 3,
    "Hearing_loss|_autosomal_recessive": 110,
    "GJB3-related_disorder|not_specified|not_provided|Erythrokeratodermia_variabilis_et_progressiva_1": 1,
    "Deafness|_digenic|_GJB2/GJB3": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2B": 1,
    "not_provided|GJB3-related_disorder|Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_dominant_nonsyndromic_hearing_loss_2B|not_specified": 1,
    "Inborn_genetic_diseases|GJB3-related_disorder": 1,
    "not_specified|Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_2B|not_provided": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_2B|not_provided|Deafness|_digenic|_GJB2/GJB3": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Inborn_genetic_diseases": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_1|not_specified|not_provided": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_1|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8": 67,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Erythrokeratodermia_variabilis_et_progressiva_1|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|GJB3-related_disorder|not_provided": 1,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_1|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_2B": 1,
    "GJB3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2B": 1,
    "Nonsyndromic_Deafness|not_provided": 2,
    "GJB3-related_disorder|not_provided": 1,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_1|not_specified": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|Erythrokeratodermia_variabilis_et_progressiva_1": 3,
    "Skin_hemangioma|Cutaneous_venous_malformation|Hepatic_hemangioma": 1,
    "Vascular_lesions": 1,
    "ZMYM6-related_disorder": 22,
    "not_provided|ZMYM6-related_disorder": 1,
    "ZMYM6-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_infantile_epileptic_spasms": 16,
    "NCDN-related_disorder|not_provided": 1,
    "NCDN-related_disorder": 4,
    "Neurodevelopmental_disorder_with_infantile_epileptic_spasms|Floating-Harbor_syndrome": 1,
    "Neurodevelopmental_disorder_with_infantile_epileptic_spasms|not_specified": 2,
    "not_specified|Neurodevelopmental_disorder_with_infantile_epileptic_spasms|NCDN-related_disorder": 1,
    "not_specified|Neurodevelopmental_disorder_with_infantile_epileptic_spasms": 1,
    "Neurodevelopmental_disorder_with_infantile_epileptic_spasms|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_infantile_epileptic_spasms": 1,
    "AGO4-related_disorder": 1,
    "not_specified|AGO4-related_disorder": 1,
    "AGO1-related_disorder|not_provided": 4,
    "AGO1-related_disorder": 7,
    "Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures|AGO1-related_disorder": 1,
    "not_provided|AGO1-related_disorder": 4,
    "Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures": 12,
    "Tremor|Severe_global_developmental_delay|Seizure|Intellectual_disability|_severe|Self-injurious_behavior|not_provided|See_cases|Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures|Inborn_genetic_diseases|Neurodevelopmental_abnormality": 1,
    "Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures|Neurodevelopmental_abnormality": 1,
    "Intellectual_disability|Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "not_provided|Intellectual_disability|Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "not_provided|AGO1-related_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures|Intellectual_disability": 1,
    "Intellectual_disability|AGO1-associated_disorder": 1,
    "Intellectual_disability|not_provided|Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "AGO1-related_disorder|not_specified": 1,
    "not_specified|not_provided|Intellectual_disability|AGO1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_language_delay_and_behavioral_abnormalities|_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "not_specified|AGO1-related_Intellectual_disability": 1,
    "not_provided|AGO3-related_disorder": 3,
    "AGO3-related_disorder": 7,
    "AGO3-related_disorder|not_provided": 2,
    "Neurodegeneration|_childhood-onset|_stress-induced|_with_variable_ataxia_and_seizures": 19,
    "Neurodegeneration|_childhood-onset|_stress-induced|_with_variable_ataxia_and_seizures|not_provided": 2,
    "ADPRS-related_disorder": 2,
    "not_provided|ADPRHL2-related_disorder": 1,
    "Neurodegeneration|_childhood-onset|_stress-induced|_with_variable_ataxia_and_seizures|ADPRS-related_disorder": 1,
    "Abdominal_distention|Progressive_sensorineural_hearing_impairment|Atypical_absence_seizure|Progressive_gait_ataxia|Bilateral_sensorineural_hearing_impairment|Axial_hypotonia|Loss_of_consciousness|Delayed_speech_and_language_development|Neurodegeneration|_childhood-onset|_stress-induced|_with_variable_ataxia_and_seizures": 1,
    "not_provided|Neurodegeneration|_childhood-onset|_stress-induced|_with_variable_ataxia_and_seizures": 2,
    "not_provided|Posterior_polymorphous_corneal_dystrophy_2|Corneal_dystrophy|_Fuchs_endothelial|_1": 1,
    "COL8A2-related_disorder": 5,
    "Posterior_polymorphous_corneal_dystrophy_2": 1,
    "COL8A2-related_disorder|not_provided": 5,
    "Corneal_dystrophy|_Fuchs_endothelial|_1": 2,
    "Corneal_dystrophy|_Fuchs_endothelial|_1|Posterior_polymorphous_corneal_dystrophy_2": 2,
    "not_provided|COL8A2-related_disorder": 1,
    "Inborn_genetic_diseases|Posterior_polymorphous_corneal_dystrophy_2": 1,
    "not_provided|Corneal_dystrophy|_Fuchs_endothelial|_1|Posterior_polymorphous_corneal_dystrophy_2": 1,
    "Fraser_syndrome_3": 122,
    "CSF3R-related_disorder": 5,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|CSF3R-related_disorder": 7,
    "not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 7,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 462,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided": 15,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified": 1,
    "Hereditary_neutrophilia|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified|not_provided": 1,
    "CSF3R-related_disorder|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 9,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Inborn_genetic_diseases": 26,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified": 10,
    "Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 11,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 14,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|CSF3R-related_disorder|not_specified": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Inborn_genetic_diseases|not_specified": 2,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|CSF3R-related_disorder|not_provided|Hereditary_neutrophilia": 1,
    "not_provided|CSF3R-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 1,
    "not_provided|not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|CSF3R-related_disorder": 1,
    "Hereditary_neutrophilia": 1,
    "not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|CSF3R-related_disorder|not_provided": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Early_T_cell_progenitor_acute_lymphoblastic_leukemia|not_provided": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified|not_provided": 7,
    "not_specified|not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 6,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified|CSF3R-related_disorder": 1,
    "CSF3R-related_disorder|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified": 3,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided|not_specified": 2,
    "Inherited_Immunodeficiency_Diseases|not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Hereditary_neutrophilia|CSF3R-Related_Disorders|CSF3R-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified": 2,
    "Severe_congenital_neutropenia": 7,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "CSF3R-related_disorder|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 3,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Hereditary_neutrophilia": 2,
    "Severe_congenital_neutropenia|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 1,
    "Hereditary_neutrophilia|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided|Inborn_genetic_diseases|CSF3R-related_disorder": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided|Hereditary_neutrophilia": 1,
    "not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided|CSF3R-related_disorder": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Hereditary_neutrophilia|not_provided|not_specified": 1,
    "Severe_congenital_neutropenia|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|not_provided": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|CSF3R-related_disorder": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_CSF3R_deficiency|Hereditary_neutrophilia|Inborn_genetic_diseases": 1,
    "not_provided|Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism": 3,
    "not_provided|not_specified|Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism|SNIP1-related_disorder": 1,
    "Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism": 3,
    "Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism|not_provided|not_specified": 1,
    "SNIP1-related_disorder|not_provided": 3,
    "Predisposition_to_dissection|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism|not_provided": 1,
    "Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism|not_provided": 1,
    "Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism|not_specified|not_provided": 1,
    "SNIP1-related_disorder|not_provided|Psychomotor_retardation|_epilepsy|_and_craniofacial_dysmorphism": 1,
    "Spermatogenic_failure_83": 1,
    "RSPO1-related_disorder|not_provided": 1,
    "RSPO1-related_disorder": 1,
    "Palmoplantar_hyperkeratosis_and_true_hermaphroditism": 1,
    "RSPO1-related_disorder|Palmoplantar_keratoderma-XX_sex_reversal-predisposition_to_squamous_cell_carcinoma_syndrome": 1,
    "not_provided|Palmoplantar_keratoderma-XX_sex_reversal-predisposition_to_squamous_cell_carcinoma_syndrome|Inborn_genetic_diseases": 1,
    "Palmoplantar_keratoderma-XX_sex_reversal-predisposition_to_squamous_cell_carcinoma_syndrome": 2,
    "Neutrophil_inclusion_bodies|CDCA8-related_condition|not_specified": 1,
    "Hearing_loss|_autosomal_dominant_88": 1,
    "Nonsyndromic_Deafness|Hearing_loss|_autosomal_dominant_88": 1,
    "MANEAL-associated_disorder": 1,
    "not_provided|YRDC-related_disorder": 4,
    "Galloway-Mowat_syndrome_10": 4,
    "YRDC-related_disorder|not_provided": 3,
    "YRDC-related_disorder": 9,
    "YRDC-related_disorder|not_specified": 1,
    "INPP5B-related_disorder": 10,
    "Dent_disease_type_2": 21,
    "INPP5B-related_disorder|not_provided": 1,
    "RRAGC-related_condition": 1,
    "Long-Olsen-Distelmaier_syndrome": 3,
    "See_cases|Long-Olsen-Distelmaier_syndrome": 1,
    "AKIRIN1-related_disorder": 2,
    "MACF1-related_disorder": 58,
    "not_provided|Inborn_genetic_diseases|MACF1-related_disorder": 6,
    "Lissencephaly_9_with_complex_brainstem_malformation|not_provided|Inborn_genetic_diseases": 2,
    "Lissencephaly_9_with_complex_brainstem_malformation": 79,
    "not_provided|Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases": 2,
    "Lissencephaly_9_with_complex_brainstem_malformation|not_provided": 16,
    "Spectraplakinopathy_type_I|Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases|not_provided": 1,
    "Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases": 8,
    "not_provided|Lissencephaly_9_with_complex_brainstem_malformation": 11,
    "not_provided|MACF1-related_disorder": 33,
    "MACF1-related_disorder|not_provided": 20,
    "MACF1-related_disorder|Lissencephaly_9_with_complex_brainstem_malformation|not_provided": 4,
    "Inborn_genetic_diseases|Lissencephaly_9_with_complex_brainstem_malformation": 4,
    "not_provided|Lissencephaly_9_with_complex_brainstem_malformation|MACF1-related_disorder": 4,
    "MACF1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Abnormal_corpus_callosum_morphology": 3,
    "Lissencephaly_9_with_complex_brainstem_malformation|MACF1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|MACF1-related_disorder": 5,
    "Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases|MACF1-related_disorder|not_provided": 2,
    "not_provided|Short_stature": 11,
    "Spectraplakinopathy_type_I|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MACF1-related_disorder|Lissencephaly_9_with_complex_brainstem_malformation": 3,
    "MACF1-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_9_with_complex_brainstem_malformation": 3,
    "MACF1-related_disorder|Lissencephaly_9_with_complex_brainstem_malformation": 1,
    "Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases|not_provided|MACF1-related_disorder": 3,
    "not_provided|MACF1-related_disorder|Inborn_genetic_diseases": 1,
    "Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases|not_provided": 4,
    "Spectraplakinopathy_type_I|not_provided|Lissencephaly_9_with_complex_brainstem_malformation": 1,
    "Spectraplakinopathy_type_I": 2,
    "Spectraplakinopathy_type_I|not_provided": 1,
    "Inborn_genetic_diseases|Epilepsy": 33,
    "Inborn_genetic_diseases|not_provided|MACF1-related_disorder|Lissencephaly_9_with_complex_brainstem_malformation": 1,
    "MACF1-related_disorder|not_provided|not_specified|Inborn_genetic_diseases|Lissencephaly_9_with_complex_brainstem_malformation": 1,
    "MACF1-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Lissencephaly_9_with_complex_brainstem_malformation|not_provided": 1,
    "Lissencephaly_9_with_complex_brainstem_malformation|MACF1-related_disorder": 1,
    "MACF1-related_disorder|not_provided|Lissencephaly_9_with_complex_brainstem_malformation": 1,
    "Lissencephaly_9_with_complex_brainstem_malformation|Lissencephaly": 1,
    "Cleft_palate|Inborn_genetic_diseases|Lissencephaly_9_with_complex_brainstem_malformation|MACF1-related_disorder|not_provided": 1,
    "MACF1-related_disorder|not_provided|Lissencephaly_9_with_complex_brainstem_malformation|Inborn_genetic_diseases": 1,
    "not_provided|Skeletal_dysplasia": 1,
    "Lissencephaly_9_with_complex_brainstem_malformation|Lissencephaly|lissencephaly_with_brainstem_hypoplasia|Lissencephaly_with_decussation_defect": 1,
    "lissencephaly_with_brainstem_hypoplasia|Lissencephaly_9_with_complex_brainstem_malformation|Lissencephaly_with_decussation_defect": 3,
    "Isolated_unilateral_hemispheric_cerebellar_hypoplasia|Facial_hemangioma|Congenital_cerebellar_hypoplasia": 1,
    "MACF1-related_disorder|not_provided|Abnormal_corpus_callosum_morphology": 1,
    "Combined_oxidative_phosphorylation_deficiency_35|TRIT1_Deficiency": 2,
    "Combined_oxidative_phosphorylation_deficiency_35": 12,
    "Combined_oxidative_phosphorylation_deficiency_35|not_provided": 4,
    "TRIT1-related_disorder": 4,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency_35": 2,
    "Combined_oxidative_phosphorylation_deficiency_35|TRIT1_Deficiency|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_35": 4,
    "Inborn_genetic_diseases|not_provided|TRIT1-related_disorder|Combined_oxidative_phosphorylation_deficiency_35": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_35|Inborn_genetic_diseases": 2,
    "Combined_oxidative_phosphorylation_deficiency_35|not_provided|TRIT1_Deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency_35|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mitochondrial_disease": 2,
    "Combined_oxidative_phosphorylation_deficiency_35|not_provided|Epileptic_encephalopathy|See_cases|TRIT1_Deficiency": 1,
    "Macrocephaly|Combined_oxidative_phosphorylation_deficiency_35|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|TRIT1-related_disorder": 2,
    "TRIT1_Deficiency|Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_deficiency_35": 1,
    "not_provided|Microcephaly_15|_primary|_autosomal_recessive": 2,
    "MFSD2A-related_disorder|not_provided": 1,
    "Microcephaly_15|_primary|_autosomal_recessive|not_provided": 2,
    "Functional_abnormality_of_male_internal_genitalia|Microcephaly|Fetal_growth_restriction|Intellectual_disability|Delayed_gross_motor_development|Hyperammonemia|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Cryptorchidism": 1,
    "not_provided|MFSD2A-related_disorder": 3,
    "Microcephaly_15|_primary|_autosomal_recessive": 10,
    "Microcephaly_15|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "MFSD2A-related_disorder": 1,
    "Microcephaly|Inborn_genetic_diseases": 5,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive": 23,
    "Neuronal_ceroid_lipofuscinosis_1": 518,
    "Neuronal_ceroid_lipofuscinosis_1|not_provided": 27,
    "not_provided|Neuronal_ceroid_lipofuscinosis_1": 33,
    "not_provided|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Neuronal_ceroid_lipofuscinosis_1": 1,
    "PPT1-related_disorder|Neuronal_ceroid_lipofuscinosis_1|not_provided|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_1|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_1": 14,
    "PPT1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_1|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_1|not_provided": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_1": 2,
    "Neuronal_ceroid_lipofuscinosis_1|Inborn_genetic_diseases": 6,
    "Neuronal_ceroid_lipofuscinosis_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_1|not_specified": 3,
    "not_specified|Neuronal_ceroid_lipofuscinosis_1": 7,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_1": 2,
    "Neuronal_ceroid_lipofuscinosis_1|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_1|PPT1-related_disorder": 2,
    "Neuronal_ceroid_lipofuscinosis_1|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 1,
    "Neuronal_ceroid_lipofuscinosis": 2443,
    "Neuronal_ceroid_lipofuscinosis_1|not_specified|not_provided": 4,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_1": 2,
    "Neuronal_ceroid_lipofuscinosis_1|Spastic_ataxia|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_1": 3,
    "not_provided|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|See_cases|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Neuronal_ceroid_lipofuscinosis_1|not_specified": 10,
    "Neuronal_ceroid_lipofuscinosis_1|not_provided|not_specified": 2,
    "PPT1-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis_1|Abnormality_of_the_nervous_system|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_1": 1,
    "PPT1-related_disorder|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_1": 1,
    "PPT1-related_disorder|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_1": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_1|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis_1|Inborn_genetic_diseases|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis_1|Neuronal_ceroid_lipofuscinosis": 3,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_1": 2,
    "not_provided|not_specified|Neuronal_ceroid_lipofuscinosis_1": 3,
    "PPT1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Central_core_myopathy|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Neuronal_ceroid_lipofuscinosis_1|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_1|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_1": 1,
    "PPT1-related_disorder|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Mandibuloacral_dysplasia|Lethal_tight_skin_contracture_syndrome": 5,
    "Mandibuloacral_dysplasia|not_provided|Lethal_tight_skin_contracture_syndrome": 1,
    "Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_B_lipodystrophy": 12,
    "Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_B_lipodystrophy|not_provided": 8,
    "Lethal_tight_skin_contracture_syndrome|not_provided": 3,
    "Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Restrictive_dermopathy_1": 3,
    "Mandibuloacral_dysplasia_with_type_B_lipodystrophy|not_provided": 2,
    "Lethal_tight_skin_contracture_syndrome|not_provided|Mandibuloacral_dysplasia_with_type_B_lipodystrophy": 1,
    "Inborn_genetic_diseases|Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_B_lipodystrophy": 1,
    "Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Lethal_tight_skin_contracture_syndrome|not_provided": 4,
    "Lethal_tight_skin_contracture_syndrome": 3,
    "Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Lethal_tight_skin_contracture_syndrome": 13,
    "not_provided|Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Lethal_tight_skin_contracture_syndrome": 4,
    "not_specified|not_provided|Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Lethal_tight_skin_contracture_syndrome": 1,
    "not_provided|Mandibuloacral_dysplasia_with_type_B_lipodystrophy": 3,
    "not_provided|Lethal_tight_skin_contracture_syndrome": 1,
    "Mandibuloacral_dysplasia|ZMPSTE24-related_disorder|not_provided|Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_B_lipodystrophy": 1,
    "not_provided|Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Restrictive_dermopathy_1": 1,
    "not_provided|ZMPSTE24-related_disorder": 1,
    "ZMPSTE24-related_disorder": 1,
    "Restrictive_dermopathy_1": 1,
    "Restrictive_dermopathy_1|ZMPSTE24-related_disorder|Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_B_lipodystrophy|not_provided": 1,
    "not_specified|ZMPSTE24-related_disorder|Mandibuloacral_dysplasia_with_type_B_lipodystrophy|Lethal_tight_skin_contracture_syndrome|not_provided": 1,
    "Mandibuloacral_dysplasia_with_type_B_lipodystrophy|ZMPSTE24-related_disorder": 1,
    "not_provided|Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_B_lipodystrophy": 3,
    "ZMPSTE24-related_disorder|not_provided": 1,
    "Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia": 1,
    "Epiphyseal_dysplasia|_multiple|_2": 27,
    "not_provided|Epiphyseal_dysplasia|_multiple|_2": 14,
    "Epiphyseal_dysplasia|_multiple|_2|not_provided": 14,
    "Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder|not_specified|Meniere_disease|not_provided|Stickler_syndrome|_type_5|Intervertebral_disc_disorder": 1,
    "Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Epiphyseal_dysplasia|_multiple|_2|not_provided|not_specified": 3,
    "Connective_tissue_disorder|Epiphyseal_dysplasia|_multiple|_2|not_specified|not_provided": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Epiphyseal_dysplasia|_multiple|_2": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5": 1,
    "not_specified|Epiphyseal_dysplasia|_multiple|_2|Connective_tissue_disorder|not_provided": 1,
    "COL9A2-related_disorder|not_specified|not_provided": 1,
    "not_specified|Epiphyseal_dysplasia|_multiple|_2|not_provided": 4,
    "Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5|not_provided|not_specified": 1,
    "not_specified|not_provided|Epiphyseal_dysplasia|_multiple|_2|Connective_tissue_disorder": 1,
    "Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder|Meniere_disease|not_specified|not_provided": 1,
    "not_specified|not_provided|COL9A2-related_disorder|Epiphyseal_dysplasia|_multiple|_2|Connective_tissue_disorder": 1,
    "Epiphyseal_dysplasia": 1,
    "COL9A2-related_disorder": 7,
    "not_provided|Stickler_syndrome": 3,
    "COL9A2-related_disorder|Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|not_provided": 1,
    "Stickler_syndrome|_type_5|not_specified|not_provided|COL9A2-related_disorder": 1,
    "Epiphyseal_dysplasia|_multiple|_2|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5": 1,
    "Inborn_genetic_diseases|not_provided|COL9A2-related_disorder": 1,
    "COL9A2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5|not_specified|not_provided|Connective_tissue_disorder": 1,
    "COL9A2-related_disorder|not_provided": 7,
    "COL9A2-related_disorder|not_provided|Stickler_syndrome|_type_5": 1,
    "not_provided|Connective_tissue_disorder|not_specified": 10,
    "Stickler_syndrome|_type_5|Epiphyseal_dysplasia|_multiple|_2|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5|not_provided": 1,
    "COL9A2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_2|Inborn_genetic_diseases|not_provided": 1,
    "Stickler_syndrome|not_provided": 5,
    "not_specified|COL9A2-related_disorder|Epiphyseal_dysplasia|_multiple|_2|not_provided|Stickler_syndrome|_type_5": 1,
    "not_provided|COL9A2-related_disorder": 2,
    "not_provided|not_specified|Epiphyseal_dysplasia|_multiple|_2": 3,
    "Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5|not_specified|not_provided": 2,
    "Epiphyseal_dysplasia|_multiple|_2|not_provided|Inborn_genetic_diseases": 2,
    "COL9A2-related_disorder|not_provided|Epiphyseal_dysplasia|_multiple|_2": 1,
    "not_provided|Stickler_syndrome|_type_5|Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder": 1,
    "Stickler_syndrome|_type_5|Epiphyseal_dysplasia|_multiple|_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_2|not_specified": 3,
    "not_provided|Epiphyseal_dysplasia|_multiple|_2|not_specified|Connective_tissue_disorder": 2,
    "Epiphyseal_dysplasia|_multiple|_2|not_provided|Inborn_genetic_diseases|Stickler_syndrome|_type_5": 1,
    "Inborn_genetic_diseases|not_provided|COL9A2-related_disorder|Connective_tissue_disorder": 1,
    "COL9A2-related_disorder|not_specified|not_provided|Epiphyseal_dysplasia|_multiple|_2": 1,
    "Intervertebral_disc_disease|_susceptibility_to|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Epiphyseal_dysplasia|_multiple|_2": 2,
    "Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5|not_provided|COL9A2-related_disorder": 1,
    "Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder|not_provided": 1,
    "Stickler_syndrome|_type_5": 1,
    "Stickler_syndrome|Epiphyseal_dysplasia|_multiple|_2|Stickler_syndrome|_type_5|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_2|not_specified|not_provided|Connective_tissue_disorder": 1,
    "not_specified|Epiphyseal_dysplasia|_multiple|_2|not_provided|Connective_tissue_disorder": 1,
    "not_specified|COL9A2-related_disorder|not_provided|Stickler_syndrome|_type_5": 1,
    "not_provided|Connective_tissue_disorder|Epiphyseal_dysplasia|_multiple|_2|not_specified|COL9A2-related_disorder": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_2|Inborn_genetic_diseases": 1,
    "COL9A2-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Meniere_disease": 1,
    "not_specified|not_provided|Epiphyseal_dysplasia|_multiple|_2": 1,
    "Inborn_genetic_diseases|COL9A2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Stickler_syndrome|_type_5|COL9A2-related_disorder": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder": 1,
    "not_specified|not_provided|COL9A2-related_disorder|Epiphyseal_dysplasia|_multiple|_2": 1,
    "Epiphyseal_dysplasia|_multiple|_2|COL9A2-related_disorder|not_specified": 1,
    "RIMS3-related_disorder": 14,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided": 6,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 10,
    "KCNQ4-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A": 35,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided|not_specified": 4,
    "not_provided|KCNQ4-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hearing_impairment|Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided": 1,
    "KCNQ4-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A|KCNQ4-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided": 3,
    "Bilateral_sensorineural_hearing_impairment|not_provided": 2,
    "KCNQ4-related_disorder": 7,
    "not_specified|Nonsyndromic_genetic_hearing_loss": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A|KCNQ4-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss": 3,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_specified": 5,
    "Nonsyndromic_genetic_hearing_loss|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "Nonsyndromic_genetic_hearing_loss|not_specified|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided|Rare_genetic_deafness": 1,
    "KCNQ4-related_disorder|not_provided": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_specified|not_provided": 3,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|Rare_genetic_deafness|not_provided": 1,
    "Hearing_impairment": 170,
    "not_provided|KCNQ4-related_disorder": 1,
    "not_provided|KCNQ4-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_2A|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|Inborn_genetic_diseases|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided|not_specified|KCNQ4-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "KCNQ4-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_2A|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_2A": 1,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency": 233,
    "not_provided|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency": 6,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|not_provided": 5,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|CTPS1-related_disorder": 2,
    "CTPS1-related_disorder|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency": 3,
    "not_specified|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency": 10,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|not_specified": 8,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|not_specified|not_provided": 2,
    "CTPS1-related_disorder|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|CTPS1-related_disorder|not_provided": 1,
    "not_specified|CTPS1-related_disorder|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|not_provided": 1,
    "CTPS1-related_disorder|not_specified|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency": 1,
    "not_provided|not_specified|Severe_combined_immunodeficiency_due_to_CTPS1_deficiency": 1,
    "Severe_combined_immunodeficiency_due_to_CTPS1_deficiency|CTPS1-related_disorder|not_specified|not_provided": 1,
    "HIVEP3-related_disorder": 69,
    "not_specified|not_provided|HIVEP3-related_disorder": 1,
    "HIVEP3-related_disorder|not_specified|not_provided": 2,
    "not_specified|HIVEP3-related_disorder|not_provided": 2,
    "not_provided|HIVEP3-related_disorder": 4,
    "HIVEP3-related_disorder|not_provided|not_specified": 2,
    "HIVEP3-related_disorder|not_provided": 4,
    "not_provided|not_specified|HIVEP3-related_disorder": 1,
    "not_provided|PPCS-related_disorder|not_specified": 2,
    "Cardiomyopathy|_dilated|_2c|not_provided": 3,
    "Leukoencephalopathy_with_vanishing_white_matter_1": 12,
    "PPCS-related_disorder|not_specified|not_provided": 2,
    "PPCS-related_disorder|not_provided": 2,
    "not_provided|not_specified|PPCS-related_disorder": 2,
    "Cardiomyopathy|_dilated|_2c": 3,
    "not_provided|PPCS-related_disorder": 1,
    "Cardiomyopathy|_dilated|_2c|Inborn_genetic_diseases|Cardiovascular_phenotype|not_provided|PPCS-related_disorder": 1,
    "YBX1-related_disorder": 3,
    "Renal_hypomagnesemia_5_with_ocular_involvement": 84,
    "Renal_hypomagnesemia_5_with_ocular_involvement|not_provided": 15,
    "Renal_Hypomagnesemia|_Recessive": 7,
    "not_provided|Renal_hypomagnesemia_5_with_ocular_involvement": 8,
    "Inborn_genetic_diseases|Renal_hypomagnesemia_5_with_ocular_involvement|not_provided": 1,
    "not_provided|Renal_hypomagnesemia_5_with_ocular_involvement|Inborn_genetic_diseases": 3,
    "not_provided|Renal_hypomagnesemia_5_with_ocular_involvement|not_specified": 1,
    "Inborn_genetic_diseases|Renal_hypomagnesemia_5_with_ocular_involvement": 3,
    "Nephrocalcinosis|Nephrolithiasis|Renal_hypomagnesemia_5_with_ocular_involvement|not_provided": 1,
    "CLDN19-related_disorder": 1,
    "Renal_hypomagnesemia_5_with_ocular_involvement|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CLDN19-related_disorder": 1,
    "Inborn_genetic_diseases|CLDN19-related_disorder|Renal_hypomagnesemia_5_with_ocular_involvement|not_provided": 1,
    "CLDN19-related_disorder|not_provided|Inborn_genetic_diseases|Renal_hypomagnesemia_5_with_ocular_involvement": 1,
    "Inborn_genetic_diseases|not_provided|Renal_hypomagnesemia_5_with_ocular_involvement": 1,
    "Renal_hypomagnesemia_5_with_ocular_involvement|Inborn_genetic_diseases": 1,
    "CLDN19-related_disorder|not_provided": 1,
    "CLDN19-related_disorder|Renal_hypomagnesemia_5_with_ocular_involvement|not_provided": 1,
    "Renal_hypomagnesemia_5_with_ocular_involvement|not_provided|CLDN19-related_disorder": 1,
    "Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta_type_8": 10,
    "not_provided|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta_type_8": 2,
    "Osteogenesis_Imperfecta|_Recessive": 28,
    "Osteogenesis_imperfecta": 151,
    "Osteogenesis_imperfecta_type_8": 622,
    "Osteogenesis_imperfecta_type_8|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_imperfecta": 4,
    "Osteogenesis_imperfecta_type_8|not_provided|P3H1-related_disorder|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_specified|Osteogenesis_imperfecta_type_8|Inborn_genetic_diseases|not_provided": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_imperfecta_type_III": 1,
    "Osteogenesis_imperfecta_type_8|Inborn_genetic_diseases": 18,
    "not_provided|Osteogenesis_imperfecta_type_8": 12,
    "Inborn_genetic_diseases|P3H1-related_disorder|Osteogenesis_imperfecta_type_8": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta_type_8": 27,
    "Osteogenesis_imperfecta_type_8|not_provided|Inborn_genetic_diseases": 1,
    "P3H1-related_disorder": 3,
    "Osteogenesis_imperfecta_type_8|not_provided": 22,
    "not_provided|P3H1-related_disorder|Osteogenesis_imperfecta_type_8": 2,
    "P3H1-related_disorder|Osteogenesis_imperfecta_type_8": 9,
    "Osteogenesis_imperfecta_type_8|P3H1-related_disorder": 5,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_8": 2,
    "not_specified|P3H1-related_disorder|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta_type_8": 1,
    "Osteogenesis_imperfecta_type_8|not_specified": 5,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III": 3,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_8|not_specified": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_8": 2,
    "Inborn_genetic_diseases|Long_QT_syndrome_12|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_provided|Osteogenesis_imperfecta_type_8|not_specified": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_8|not_provided|P3H1-related_disorder": 1,
    "not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive": 1,
    "P3H1-related_disorder|Osteogenesis_Imperfecta|_Recessive|not_provided|Osteogenesis_imperfecta_type_8": 1,
    "Inborn_genetic_diseases|not_provided|P3H1-related_disorder|Osteogenesis_imperfecta_type_8": 1,
    "not_specified|Osteogenesis_imperfecta_type_8": 6,
    "not_provided|Osteogenesis_imperfecta_type_8|P3H1-related_disorder": 2,
    "Osteogenesis_imperfecta_type_8|P3H1-related_disorder|not_provided": 1,
    "Osteogenesis_imperfecta_type_8|not_specified|not_provided|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_8": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8": 3,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|not_provided": 1,
    "not_specified|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta|not_provided": 1,
    "P3H1-related_disorder|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta_type_8": 1,
    "Osteogenesis_imperfecta|not_specified|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive": 1,
    "P3H1-related_disorder|Osteogenesis_imperfecta_type_8|not_specified|not_provided": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|not_specified|not_provided": 1,
    "P3H1-related_disorder|not_provided|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_provided|not_specified|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta_type_8": 1,
    "P3H1-related_disorder|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_8|P3H1-related_disorder|not_specified": 1,
    "P3H1-related_disorder|not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8|not_provided": 1,
    "Osteogenesis_imperfecta_type_8|not_specified|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta": 2,
    "not_provided|Inborn_genetic_diseases|Osteogenesis_imperfecta_type_8|P3H1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Osteogenesis_imperfecta_type_8": 1,
    "P3H1-related_disorder|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_8": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_imperfecta|not_specified|not_provided": 1,
    "Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|not_specified": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8|not_specified|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_specified|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8": 1,
    "Inborn_genetic_diseases|P3H1-related_disorder": 1,
    "Osteogenesis_Imperfecta|_Recessive|not_specified|Osteogenesis_imperfecta_type_8": 1,
    "not_specified|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta_type_8": 2,
    "not_specified|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|Osteogenesis_imperfecta|not_provided": 1,
    "Osteogenesis_imperfecta_type_8|P3H1-related_disorder|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta_type_8|not_provided|P3H1-related_disorder|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive|not_specified": 1,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_8|Osteogenesis_Imperfecta|_Recessive": 1,
    "Osteogenesis_imperfecta_type_8|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_8|Inborn_genetic_diseases": 1,
    "not_specified|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_provided|Osteogenesis_Imperfecta|_Recessive": 4,
    "SVBP-related_disorder": 1,
    "Neurodevelopmental_disorder_with_ataxia|Microcephaly|Intellectual_disability|Lower_limb_spasticity|Neurodevelopmental_disorder_with_ataxia|_hypotonia|_and_microcephaly": 1,
    "Neurodevelopmental_disorder_with_ataxia|_hypotonia|_and_microcephaly": 2,
    "Microcephaly|Intellectual_disability|Lower_limb_spasticity|Neurodevelopmental_disorder_with_ataxia|_hypotonia|_and_microcephaly": 1,
    "ERMAP-related_disorder": 7,
    "Antigen_in_Scianna_blood_group_system": 1,
    "not_specified|SCIANNA_BLOOD_GROUP_SYSTEM|_SC:-1|2": 1,
    "RADIN_BLOOD_GROUP_ANTIGEN": 1,
    "SCIANNA_BLOOD_GROUP_SYSTEM|_SC:-1|-2": 1,
    "Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency": 32,
    "Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9": 8,
    "Dystonia_9|not_provided|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|not_provided": 2,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9": 3,
    "Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Dystonic_disorder|GLUT1_deficiency_syndrome": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "SLC2A1-related_disorder|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided": 4,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_provided": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 19,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive": 467,
    "not_provided|not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2": 19,
    "not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin": 2,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "not_specified|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 3,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Dystonia_9|not_provided|Increased_muscle_glycogen_content|Myopathy|Muscle_weakness|Migraine|Abnormality_of_the_musculature|Myalgia|Exercise-induced_myalgia|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided": 2,
    "SLC2A1-related_disorder|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|not_provided|Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided": 25,
    "not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|not_specified|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Encephalopathy_due_to_GLUT1_deficiency": 43,
    "Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Dystonia_9|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|not_provided|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Dystonia_9": 11,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "SLC2A1-related_disorder": 10,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_specified": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 6,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases": 3,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 5,
    "not_specified|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 5,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided": 1,
    "Seizure|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 4,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Dystonia_9|Inborn_genetic_diseases|Encephalopathy_due_to_GLUT1_deficiency|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Inborn_genetic_diseases|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_provided|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_specified": 2,
    "not_provided|Dystonia_9": 1,
    "SLC2A1-related_disorder|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided": 1,
    "SLC2A1-related_disorder|not_provided|See_cases|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "not_specified|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2": 2,
    "Encephalopathy_due_to_GLUT1_deficiency|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 5,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_specified": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|not_specified|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|not_provided|not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|not_specified|Dystonia_9|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes": 21,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided": 1,
    "Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome|Inborn_genetic_diseases|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|intellectual_deficiency|Microcephaly|Inborn_genetic_diseases|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Dystonia_9|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome|Inborn_genetic_diseases|Dystonic_disorder|not_specified|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_specified|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome": 3,
    "SLC2A1-related_disorder|Dystonia_9|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|Dystonia_9|Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9": 1,
    "Dystonia_9|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Seizure": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|not_specified|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Epilepsy_with_myoclonic_atonic_seizures": 598,
    "Inborn_genetic_diseases|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|not_provided": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|SLC2A1-related_disorder|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|not_provided": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|SLC2A1-related_disorder|not_specified": 1,
    "GLUT1_deficiency_syndrome|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Intellectual_disability": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Microcephaly|Abnormality_of_metabolism/homeostasis|Intellectual_disability": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_specified|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|Seizure": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Inborn_genetic_diseases|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|GLUT1_deficiency_syndrome_1|_autosomal_recessive|SLC2A1-related_disorder": 1,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Parkinsonian_disorder": 1,
    "not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Dystonia_9|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "SLC2A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "not_specified|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_provided": 2,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|Inborn_genetic_diseases": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Strabismus|Seizure|Global_developmental_delay|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|not_provided": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Intellectual_disability|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|not_specified": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Inborn_genetic_diseases": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin": 2,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_specified": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|Dystonia_9|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|not_specified": 1,
    "Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "SLC2A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive|SLC2A1-related_disorder": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|SLC2A1-related_disorder|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided": 1,
    "SLC2A1-related_disorder|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 2,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|not_provided|SLC2A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Seizure": 1,
    "Dystonia_9|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_provided": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|SLC2A1-related_disorder|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "SLC2A1-related_disorder|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_specified|Dystonia_9|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided": 2,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 2,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Intellectual_disability|Encephalopathy_due_to_GLUT1_deficiency": 2,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Inborn_genetic_diseases|not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_specified|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Cerebellar_ataxia|Global_developmental_delay|Myoclonus|Microcephaly|Seizure": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|Intellectual_disability": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency": 3,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|not_specified|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Inborn_genetic_diseases": 1,
    "Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_provided|Paroxysmal_dystonia|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases": 1,
    "not_provided|GLUT1_deficiency_syndrome|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "SLC2A1-related_disorder|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Chromosome_17q23.1-q23.2_deletion_syndrome|not_provided|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9": 1,
    "Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|SLC2A1-related_disorder|not_provided": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Inborn_genetic_diseases|SLC2A1-related_disorder|not_specified|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|not_provided": 1,
    "Seizure|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2|SLC2A1-related_disorder": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|SLC2A1-related_disorder": 1,
    "SLC2A1-related_disorder|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_provided|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Developmental_disorder|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Intellectual_disability": 1,
    "not_provided|Dystonia_9|not_specified|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|SLC2A1-related_disorder": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1": 47,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_specified": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|not_specified|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Inborn_genetic_diseases|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_provided|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "not_specified|not_provided|Dystonia_9|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Hereditary_cryohydrocytosis_with_reduced_stomatin|SLC2A1-related_disorder|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Seizure": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided|not_specified|Inborn_genetic_diseases|Dystonia_9": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Inborn_genetic_diseases|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Inborn_genetic_diseases|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_provided|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_specified|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Dystonia_9": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Hereditary_cryohydrocytosis_with_reduced_stomatin|not_specified|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2": 1,
    "not_specified|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|Dystonia_9": 1,
    "SLC2A1-related_disorder|not_provided|GLUT1_deficiency_syndrome_1|_autosomal_recessive|Encephalopathy_due_to_GLUT1_deficiency|GLUT1_deficiency_syndrome": 1,
    "Encephalopathy_due_to_GLUT1_deficiency|not_specified|Hereditary_cryohydrocytosis_with_reduced_stomatin|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Childhood_onset_GLUT1_deficiency_syndrome_2|Dystonia_9": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Dystonia_9|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonia_9|not_provided|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12": 1,
    "GLUT1_deficiency_syndrome|Dystonic_disorder": 8,
    "Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|GLUT1_deficiency_syndrome|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonic_disorder|Encephalopathy_due_to_GLUT1_deficiency|Childhood_onset_GLUT1_deficiency_syndrome_2|not_provided": 1,
    "GLUT1_deficiency_syndrome|Dystonic_disorder|not_provided": 1,
    "GLUT1_deficiency_syndrome|not_provided|Dystonia_9|Epilepsy|_idiopathic_generalized|_susceptibility_to|_12|Hereditary_cryohydrocytosis_with_reduced_stomatin|Dystonic_disorder|Childhood_onset_GLUT1_deficiency_syndrome_2|Encephalopathy_due_to_GLUT1_deficiency": 1,
    "CFAP57-related_disorder": 27,
    "not_provided|CFAP57-related_disorder": 2,
    "Primary_ciliary_dyskinesia": 18711,
    "CFAP57-related_disorder|not_specified": 1,
    "Lymphatic_malformation_11": 3,
    "TIE1-related_disorder": 2,
    "not_specified|TIE1-related_disorder": 1,
    "Congenital_amegakaryocytic_thrombocytopenia": 101,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 304,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 215,
    "Inborn_genetic_diseases|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 4,
    "Primary_myelofibrosis|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|MPL-related_disorder|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified|not_provided|Thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_1": 8,
    "Thrombocythemia_1|MPL-related_disorder|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_1|Congenital_amegakaryocytic_thrombocytopenia_1|not_provided|Essential_thrombocythemia|not_specified": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder": 4,
    "not_provided|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis|MPL-related_disorder|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Inborn_genetic_diseases": 7,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|MPL-related_disorder": 2,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided": 9,
    "MPL-related_disorder|Thrombocythemia_2|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia|not_specified": 1,
    "Thrombocythemia_1|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "not_specified|Congenital_amegakaryocytic_thrombocytopenia_1|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_1|not_provided|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Thrombocythemia_2|Primary_myelofibrosis": 2,
    "not_specified|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 5,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Primary_myelofibrosis|Thrombocythemia_2|not_specified|not_provided": 1,
    "MPL-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis|Thrombocythemia_2": 16,
    "Thrombocytopenia|not_specified": 3,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|MPL-related_disorder|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocytopenia|Abnormal_bleeding": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Primary_myelofibrosis|Thrombocythemia_2|not_specified|not_provided|Thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Thrombocythemia_2|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "not_provided|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Primary_myelofibrosis": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified|Primary_myelofibrosis|Thrombocythemia_2|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder|not_provided": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 4,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified|not_provided|Congenital_amegakaryocytic_thrombocytopenia_1": 2,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_2|Primary_myelofibrosis|not_provided": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Primary_myelofibrosis|not_specified|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided|MPL-related_disorder": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1": 5,
    "not_specified|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided": 1,
    "not_specified|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 3,
    "MPL-related_disorder": 4,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Primary_myelofibrosis|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Thrombocythemia_2|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder|Thrombocythemia_2|Primary_myelofibrosis": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Inborn_genetic_diseases|not_provided|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "not_provided|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder|not_provided|not_specified": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Inborn_genetic_diseases|MPL-related_disorder": 1,
    "Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|not_provided|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|MPL-related_disorder|Primary_myelofibrosis|Thrombocythemia_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 2,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia_1|MPL-related_disorder|not_specified|not_provided": 1,
    "MPL-related_disorder|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|not_specified|not_provided|Essential_thrombocythemia|MPL-related_disorder": 2,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder|Thrombocythemia_2|Inborn_genetic_diseases": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided|Thrombocythemia_1|not_specified": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_1": 3,
    "Thrombocytopenia|Abnormal_bleeding|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified": 3,
    "Thrombocythemia_2|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided": 1,
    "not_provided|not_specified|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Congenital_amegakaryocytic_thrombocytopenia|not_specified": 1,
    "Thrombocythemia_1|Congenital_amegakaryocytic_thrombocytopenia": 22,
    "Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified|Thrombocythemia_1|not_provided|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Primary_myelofibrosis|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_1|Essential_thrombocythemia|MPL-related_disorder": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis|Thrombocythemia_2|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Thrombocythemia_1|MPL-related_disorder|not_provided": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder|not_specified|Abnormal_bleeding|Thrombocytopenia|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "not_specified|Congenital_amegakaryocytic_thrombocytopenia|not_provided|Essential_thrombocythemia|Thrombocythemia_1|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Primary_myelofibrosis|Essential_thrombocythemia|not_specified|Thrombocythemia_1|not_provided|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Primary_myelofibrosis": 1,
    "not_provided|not_specified|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|not_provided|Essential_thrombocythemia|MPL-related_disorder": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Primary_myelofibrosis|Thrombocythemia_2": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|MPL-related_disorder|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder|not_provided|Thrombocythemia_1": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|not_provided|MPL-related_disorder": 1,
    "Thrombocythemia_2|not_provided|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "Myelofibrosis_with_myeloid_metaplasia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Myelofibrosis_with_myeloid_metaplasia|Essential_thrombocythemia|Thrombocythemia_2|_somatic": 1,
    "Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Primary_myelofibrosis|not_provided": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia_1|MPL-related_disorder|not_specified|not_provided|Thrombocythemia_1": 1,
    "Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_2|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia_1|MPL-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Thrombocythemia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_provided|Thrombocythemia_1": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_2": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Thrombocythemia_2": 1,
    "not_specified|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|MPL-related_disorder": 1,
    "not_provided|MPL-related_disorder": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia": 1,
    "not_provided|Congenital_amegakaryocytic_thrombocytopenia|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Essential_thrombocythemia": 1,
    "not_specified|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Thrombocythemia_1": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|not_specified|not_provided|Thrombocythemia_1": 1,
    "Thrombocythemia_1|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Thrombocythemia_2": 1,
    "Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia_1|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Inborn_genetic_diseases|not_specified": 1,
    "Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1|Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia": 1,
    "not_specified|not_provided|Congenital_amegakaryocytic_thrombocytopenia|Essential_thrombocythemia|Thrombocythemia_1": 1,
    "Thrombocythemia_2|Congenital_amegakaryocytic_thrombocytopenia|Primary_myelofibrosis|Essential_thrombocythemia|MPL-related_disorder": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|Thrombocythemia_2|Primary_myelofibrosis|Congenital_amegakaryocytic_thrombocytopenia_1": 1,
    "Essential_thrombocythemia|Congenital_amegakaryocytic_thrombocytopenia|not_specified": 1,
    "Oocyte_maturation_defect_14": 11,
    "not_provided|Ichthyotic_keratoderma|_spasticity|_hypomyelination|_and_dysmorphic_facial_features": 1,
    "ELOVL1-related_disorder": 1,
    "Ichthyotic_keratoderma|_spasticity|_hypomyelination|_and_dysmorphic_facial_features": 1,
    "ELOVL1-related_disorder|not_provided": 3,
    "not_provided|ELOVL1-related_disorder|Optic_atrophy": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided": 84,
    "not_provided|SZT2-related_disorder|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_18": 57,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_18": 45,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|Inborn_genetic_diseases": 46,
    "Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases|not_provided": 55,
    "SZT2-related_disorder|not_provided": 8,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_18|not_provided": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18": 68,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases": 46,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_provided": 73,
    "Developmental_and_epileptic_encephalopathy|_18|not_specified|SZT2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_18|SZT2-related_disorder|Inborn_genetic_diseases|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18": 39,
    "SZT2-related_disorder|Developmental_and_epileptic_encephalopathy|_18|not_provided": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_specified|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|Inborn_genetic_diseases|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|not_specified|SZT2-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_spherocytosis_type_3": 14,
    "not_specified|Developmental_and_epileptic_encephalopathy|_18|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|SZT2-related_disorder|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|SZT2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_18|not_specified": 2,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_18": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_provided|not_specified": 4,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_specified": 2,
    "not_provided|SZT2-related_disorder": 3,
    "SZT2-related_disorder|Self-limited_epilepsy_with_centrotemporal_spikes|Developmental_and_epileptic_encephalopathy|_18|See_cases|not_provided": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|_18|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|not_specified": 7,
    "SZT2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_provided": 4,
    "SZT2-related_disorder": 7,
    "SZT2-related_disorder|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_18": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|SZT2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|SZT2-related_disorder|Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases": 2,
    "not_provided|SZT2-related_disorder|Developmental_and_epileptic_encephalopathy|_18": 3,
    "not_provided|Severe_hydrocephalus|Encephalocele": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|SZT2-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases|SZT2-related_disorder": 2,
    "not_provided|Self-limited_epilepsy_with_centrotemporal_spikes": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_18": 1,
    "not_provided|Inborn_genetic_diseases|Self-limited_epilepsy_with_centrotemporal_spikes": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_18": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|SZT2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_18": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_18|SZT2-related_disorder|not_provided": 4,
    "not_provided|SZT2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_specified|not_provided|Inborn_genetic_diseases": 4,
    "SZT2-related_disorder|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_specified|Inborn_genetic_diseases|not_provided": 2,
    "SZT2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_18|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Inborn_genetic_diseases": 1,
    "Severe_hydrocephalus|Encephalocele": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "SZT2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_18": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_provided|Inborn_genetic_diseases|SZT2-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|SZT2-related_disorder|Developmental_and_epileptic_encephalopathy|_18|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_specified|not_provided": 3,
    "SZT2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_provided": 1,
    "not_provided|not_specified|SZT2-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_18": 1,
    "Inborn_genetic_diseases|SZT2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_18": 2,
    "SZT2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_specified": 1,
    "SZT2-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18": 1,
    "SZT2-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18": 1,
    "Inborn_genetic_diseases|SZT2-related_disorder|not_provided": 2,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_provided": 2,
    "SZT2-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_18": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_18|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_18|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_18|not_specified|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18": 1,
    "not_specified|SZT2-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_18|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_provided|SZT2-related_disorder": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy|_18|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_18|not_specified|not_provided|SZT2-related_disorder": 1,
    "Obesity|Global_developmental_delay|Generalized_epilepsy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_18|SZT2-related_disorder": 1,
    "PTPRF-related_disorder": 23,
    "not_provided|PTPRF-related_disorder": 4,
    "PTPRF-related_disorder|not_provided": 2,
    "Breasts_and/or_nipples|_aplasia_or_hypoplasia_of|_2": 1,
    "not_specified|PTPRF-related_disorder": 1,
    "not_provided|Breasts_and/or_nipples|_aplasia_or_hypoplasia_of|_2": 1,
    "Developmental_and_epileptic_encephalopathy|_15": 6,
    "Developmental_and_epileptic_encephalopathy": 9655,
    "Developmental_and_epileptic_encephalopathy|not_specified": 235,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 205,
    "Intellectual_disability|_autosomal_recessive_12": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 245,
    "ST3GAL3-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_15|Intellectual_disability|_autosomal_recessive_12|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_15|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 26,
    "not_specified|Intellectual_disability|_autosomal_recessive_12|not_provided|Developmental_and_epileptic_encephalopathy|_15": 1,
    "ST3GAL3-related_disorder": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy": 575,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_15": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 40,
    "Developmental_and_epileptic_encephalopathy|Intellectual_disability": 2,
    "Developmental_and_epileptic_encephalopathy|Intellectual_disability|_autosomal_recessive_12|Developmental_and_epileptic_encephalopathy|_15": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_12|Developmental_and_epileptic_encephalopathy|_15|not_provided|Generalized_myoclonic_seizure|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy": 177,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_15|Intellectual_disability|_autosomal_recessive_12|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_15|Intellectual_disability|_autosomal_recessive_12|not_specified|Epilepsy_due_to_perinatal_stroke": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided": 655,
    "Developmental_and_epileptic_encephalopathy|ST3GAL3-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 20,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_15": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided": 12,
    "not_provided|Developmental_and_epileptic_encephalopathy|ST3GAL3-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|not_specified": 12,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Intellectual_disability|_autosomal_recessive_12|Developmental_and_epileptic_encephalopathy|_15|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 59,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 12,
    "Intellectual_disability|_autosomal_recessive_12|Developmental_and_epileptic_encephalopathy|_15": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|not_specified": 21,
    "not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 15,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy": 4,
    "not_specified|Developmental_and_epileptic_encephalopathy|ST3GAL3-related_disorder": 1,
    "ST3GAL3-related_disorder|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_15|not_specified|Developmental_and_epileptic_encephalopathy|Intellectual_disability|_autosomal_recessive_12|not_provided": 1,
    "ST3GAL3-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_15|Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Intellectual_disability|_autosomal_recessive_12": 1,
    "Intellectual_disability|_autosomal_recessive_12|Intellectual_disability|_severe|Difficulty_walking|Prolonged_neonatal_jaundice|Frequent_falls|Aggressive_behavior": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_12": 1,
    "Developmental_and_epileptic_encephalopathy|Intellectual_disability|_autosomal_recessive_12|Developmental_and_epileptic_encephalopathy|_15|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 32,
    "ST3GAL3-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_15|Intellectual_disability|_autosomal_recessive_12|not_provided": 1,
    "IPO13-related_disorder": 1,
    "not_specified|IPO13-related_disorder": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_2": 2,
    "Macrocephaly|Intellectual_disability|Global_developmental_delay": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_2|Ventricular_septal_defect|Global_developmental_delay|Short_stature": 1,
    "Ventricular_septal_defect|Global_developmental_delay|Short_stature|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_2": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_2|diphthamide-deficiency_syndrome": 1,
    "Atypical_glycine_encephalopathy": 219,
    "Atypical_glycine_encephalopathy|Inborn_genetic_diseases": 11,
    "not_provided|Atypical_glycine_encephalopathy": 5,
    "SLC6A9-related_disorder": 5,
    "Atypical_glycine_encephalopathy|not_provided": 7,
    "Atypical_glycine_encephalopathy|not_provided|SLC6A9-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Atypical_glycine_encephalopathy": 1,
    "Atypical_glycine_encephalopathy|not_specified|not_provided": 1,
    "SLC6A9-related_disorder|Atypical_glycine_encephalopathy": 2,
    "Inborn_genetic_diseases|Atypical_glycine_encephalopathy": 3,
    "not_provided|Atypical_glycine_encephalopathy|SLC6A9-related_disorder": 1,
    "Prostate_cancer|Atypical_glycine_encephalopathy": 1,
    "Atypical_glycine_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|SLC6A9-related_disorder|not_provided|Atypical_glycine_encephalopathy": 1,
    "Atypical_glycine_encephalopathy|SLC6A9-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Atypical_glycine_encephalopathy": 1,
    "Intellectual_disability|Abnormal_facial_shape|Seizure": 2,
    "Profound_global_developmental_delay|Generalized_hypotonia": 1,
    "DMAP1-associated_disorder": 2,
    "RNF220-related_condition": 1,
    "Leukodystrophy|_hypomyelinating|_23|_with_ataxia|_deafness|_liver_dysfunction|_and_dilated_cardiomyopathy": 3,
    "Craniotubular_dysplasia|_Ikegawa_type": 1,
    "Craniotubular_dysplasia|_Ikegawa_type|TMEM53-related_craniotubular_dysplasia": 2,
    "TMEM53-related_disorder": 1,
    "RNU5F-1-associated_neurodevelopmental_disorder|not_provided": 1,
    "PTCH2-related_disorder": 8,
    "Gorlin_syndrome": 2521,
    "not_provided|Gorlin_syndrome": 58,
    "PTCH2-related_disorder|Gorlin_syndrome": 18,
    "Gorlin_syndrome|not_specified": 59,
    "Gorlin_syndrome|PTCH2-related_disorder": 15,
    "Gorlin_syndrome|Breast_carcinoma": 1,
    "See_cases|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "Gorlin_syndrome|not_provided": 42,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 12,
    "Basal_cell_nevus_syndrome_1": 27,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 10,
    "Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 5,
    "not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Medulloblastoma": 1,
    "Basal_cell_carcinoma|_somatic": 7,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|not_specified|Gorlin_syndrome": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|PTCH2-related_disorder|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|PTCH2-related_disorder": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|Gorlin_syndrome|not_specified": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|Gorlin_syndrome": 7,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1": 37,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|Gorlin_syndrome|not_specified|PTCH2-related_disorder": 1,
    "not_specified|Gorlin_syndrome|PTCH2-related_disorder": 3,
    "not_provided|Gorlin_syndrome|not_specified": 2,
    "not_specified|Gorlin_syndrome": 40,
    "Gorlin_syndrome|not_provided|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1": 2,
    "Gorlin_syndrome|not_specified|not_provided": 4,
    "Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 8,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|not_specified": 1,
    "not_specified|Gorlin_syndrome|Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Gorlin_syndrome|PTCH2-related_disorder|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Medulloblastoma": 1,
    "Gorlin_syndrome|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 8,
    "not_provided|Gorlin_syndrome|Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1": 2,
    "PTCH2-related_disorder|not_specified": 2,
    "Gorlin_syndrome|PTCH2-related_disorder|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 1,
    "Gorlin_syndrome|Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1": 5,
    "Gorlin_syndrome|not_provided|not_specified": 2,
    "Basal_cell_nevus_syndrome_1|not_specified|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|PTCH2-related_disorder": 3,
    "not_specified|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 3,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided|Basal_cell_nevus_syndrome_1": 1,
    "Familial_cancer_of_breast": 6258,
    "PTCH2-related_disorder|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 1,
    "Gorlin_syndrome|not_specified|Basal_cell_nevus_syndrome_1": 1,
    "Gorlin_syndrome|Basal_cell_nevus_syndrome_1": 8,
    "not_specified|Gorlin_syndrome|not_provided|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Diffuse_midline_glioma|_H3_K27-altered": 6,
    "not_specified|Gorlin_syndrome|not_provided": 2,
    "Oromandibular-limb_hypogenesis_spectrum|Gorlin_syndrome": 1,
    "PTCH2-related_disorder|not_specified|Gorlin_syndrome": 1,
    "not_provided|PTCH2-related_disorder|Gorlin_syndrome": 1,
    "Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_specified|PTCH2-related_disorder": 1,
    "Gorlin_syndrome|not_provided|PTCH2-related_disorder": 4,
    "not_specified|not_provided|Gorlin_syndrome|PTCH2-related_disorder": 1,
    "PTCH2-related_disorder|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Medulloblastoma": 1,
    "not_specified|Gorlin_syndrome|Basal_cell_nevus_syndrome_1": 1,
    "not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|PTCH2-related_disorder": 1,
    "not_provided|not_specified|Gorlin_syndrome": 4,
    "Duplication_of_the_pituitary_gland": 1,
    "Gorlin_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Gorlin_syndrome|PTCH2-related_disorder|not_provided": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1": 1,
    "PTCH2-related_disorder|Gorlin_syndrome|not_provided": 1,
    "Basal_cell_nevus_syndrome_1|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|PTCH2-related_disorder": 1,
    "PTCH2-related_disorder|not_provided|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Gorlin_syndrome|Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1": 9,
    "Gorlin_syndrome|not_specified|Breast_carcinoma|PTCH2-related_disorder": 1,
    "Basal_cell_nevus_syndrome_1|not_specified|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 1,
    "Gorlin_syndrome|not_specified|PTCH2-related_disorder": 1,
    "Gorlin_syndrome|PTCH2-related_disorder|Basal_cell_nevus_syndrome_1": 1,
    "Medulloblastoma|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided|Gorlin_syndrome|PTCH2-related_disorder": 1,
    "not_specified|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|PTCH2-related_disorder": 1,
    "Gorlin_syndrome|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Medulloblastoma|Basal_cell_nevus_syndrome_1|not_specified|not_provided|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 1,
    "Vanishing_white_matter_disease": 168,
    "Vanishing_white_matter_disease|not_provided": 44,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1|not_provided|See_cases": 1,
    "not_provided|not_specified|Vanishing_white_matter_disease": 2,
    "Leukoencephalopathy_with_vanishing_white_matter_3": 8,
    "not_provided|Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_3": 2,
    "Vanishing_white_matter_disease|not_provided|EIF2B3-related_disorder": 4,
    "not_specified|Vanishing_white_matter_disease|not_provided": 3,
    "not_specified|Vanishing_white_matter_disease": 1,
    "not_specified|Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_3|not_provided": 2,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_3|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Vanishing_white_matter_disease": 2,
    "Vanishing_white_matter_disease|not_specified|not_provided": 3,
    "not_provided|Leukoencephalopathy_with_vanishing_white_matter_3": 1,
    "Vanishing_white_matter_disease|not_provided|Inborn_genetic_diseases": 1,
    "Vanishing_white_matter_disease|EIF2B3-related_disorder|Leukoencephalopathy_with_vanishing_white_matter_3|not_provided": 1,
    "not_specified|not_provided|Vanishing_white_matter_disease": 9,
    "Vanishing_white_matter_disease|not_specified|not_provided|EIF2B3-related_disorder": 1,
    "not_provided|Vanishing_white_matter_disease|EIF2B3-related_disorder": 1,
    "EIF2B3-related_disorder|not_provided|Vanishing_white_matter_disease|not_specified": 1,
    "not_provided|EIF2B3-related_disorder": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_3|Vanishing_white_matter_disease|not_provided|EIF2B3-related_disorder|Inborn_genetic_diseases": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "not_provided|Vanishing_white_matter_disease": 67,
    "Porphyria_cutanea_tarda|not_provided": 1,
    "Porphyria_cutanea_tarda": 6,
    "Familial_porphyria_cutanea_tarda": 21,
    "UROD-related_inherited_porphyria|UROD-related_disorder": 1,
    "Familial_porphyria_cutanea_tarda|not_specified|not_provided": 1,
    "Familial_porphyria_cutanea_tarda|not_provided": 7,
    "Familial_porphyria_cutanea_tarda|UROD-related_disorder|not_provided": 2,
    "UROD-related_disorder": 6,
    "not_provided|Familial_porphyria_cutanea_tarda": 13,
    "not_provided|Hepatoerythropoietic_porphyria": 1,
    "Porphyria_cutanea_tarda|Familial_porphyria_cutanea_tarda": 1,
    "Hepatoerythropoietic_porphyria|not_provided": 1,
    "UROD-related_disorder|Familial_porphyria_cutanea_tarda|not_provided": 1,
    "not_specified|Familial_porphyria_cutanea_tarda|not_provided": 1,
    "not_provided|UROD-related_disorder": 1,
    "not_provided|Porphyria_cutanea_tarda|Familial_porphyria_cutanea_tarda|Hepatoerythropoietic_porphyria": 1,
    "Hepatoerythropoietic_porphyria": 1,
    "Sporadic_porphyria_cutanea_tarda|not_provided|Hepatoerythropoietic_porphyria": 1,
    "not_provided|Familial_porphyria_cutanea_tarda|UROD-related_disorder": 1,
    "UROD-related_disorder|Familial_porphyria_cutanea_tarda|not_specified|not_provided": 1,
    "not_provided|Familial_porphyria_cutanea_tarda|not_specified": 1,
    "Normal_pregnancy": 36,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Spastic_paraplegia": 1,
    "Spastic_paraplegia": 8295,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 1,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 174,
    "HPDL-related_disorder|not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 1,
    "Inborn_genetic_diseases|Spastic_ataxia": 1,
    "not_provided|Spastic_paraplegia_83|_autosomal_recessive|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Spastic_ataxia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 3,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Spastic_paraplegia": 5,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 3,
    "not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided": 299,
    "not_provided|Spastic_paraplegia": 271,
    "not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 7,
    "Spastic_paraplegia_83|_autosomal_recessive|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 2,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Spastic_paraplegia_83|_autosomal_recessive|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases": 184,
    "Spastic_paraplegia_83|_autosomal_recessive": 1,
    "HPDL-related_disorder": 1,
    "not_provided|Spastic_paraplegia_83|_autosomal_recessive|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 1,
    "Familial_adenomatous_polyposis_2": 732,
    "Familial_adenomatous_polyposis_2|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 71,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 528,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 426,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_provided": 29,
    "not_provided|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 31,
    "Gastric_cancer|Familial_adenomatous_polyposis_2": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 27,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 36,
    "Familial_adenomatous_polyposis_2|not_specified|Hereditary_cancer-predisposing_syndrome": 11,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 19,
    "MUTYH-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 2,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 9,
    "not_specified|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 12,
    "MUTYH-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 1,
    "Gastric_cancer": 129,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2": 30,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Gastric_cancer": 1,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_2": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2|not_provided": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_2": 5,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 10,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Gastric_cancer|not_provided": 2,
    "Familial_adenomatous_polyposis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 16,
    "not_specified|Familial_adenomatous_polyposis_2": 9,
    "MUTYH-related_disorder": 3,
    "MUTYH-related_disorder|Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Pilomatrixoma|Familial_adenomatous_polyposis_2|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 5,
    "Familial_adenomatous_polyposis_2|not_specified": 15,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Familial_adenomatous_polyposis_2": 5,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided|MUTYH-related_disorder": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 12,
    "not_specified|not_provided|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 5,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 6,
    "not_provided|Familial_adenomatous_polyposis_2": 11,
    "Familial_adenomatous_polyposis_2|not_provided": 8,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_specified|not_provided": 5,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Carcinoma_of_colon": 1,
    "Malignant_tumor_of_breast|not_provided|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|Colorectal_polyposis": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|MUTYH-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Gastric_cancer": 4,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Carcinoma_of_colon": 1,
    "not_specified|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2|Gastric_cancer": 1,
    "not_provided|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 4,
    "Carcinoma_of_colon|not_provided|not_specified|Pilomatrixoma|Neoplasm_of_stomach|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_2": 17,
    "Familial_colorectal_cancer_type_X|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 1,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2|MUTYH-related_disorder|not_specified": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma|Carcinoma_of_colon": 1,
    "Malignant_tumor_of_breast": 96,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_specified": 11,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2": 3,
    "not_provided|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 5,
    "Hereditary_cancer-predisposing_syndrome|See_cases|Familial_adenomatous_polyposis_2": 1,
    "not_specified|Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_specified": 3,
    "Familial_adenomatous_polyposis_2|not_provided|MUTYH-related_disorder|Hereditary_cancer|Carcinoma_of_colon|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "MUTYH-related_disorder|not_provided|not_specified|Familial_colorectal_cancer_type_X|Carcinoma_of_colon|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified": 354,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Pilomatrixoma|Neoplasm_of_stomach|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_adenomatous_polyposis_2|Neoplasm_of_stomach": 1,
    "MUTYH-related_disorder|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|B_lymphoblastic_leukemia_lymphoma|_no_ICD-O_subtype|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Small_intestine_carcinoid|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Familial_adenomatous_polyposis_2|Gastric_cancer|MUTYH-related_disorder|Diffuse_midline_glioma|_H3_K27-altered|Neoplasm_of_stomach|Pilomatrixoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Carcinoma_of_colon|Familial_colorectal_cancer|Colorectal_adenomatous_polyposis|_autosomal_recessive|_with_pilomatricomas|Ovarian_carcinoma|Colon_cancer|Breast_carcinoma|Endometrial_cancer": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|MUTYH-related_disorder|not_provided|Familial_adenomatous_polyposis_2": 1,
    "Familial_adenomatous_polyposis_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Carcinoma_of_colon|Familial_colorectal_cancer|Familial_adenomatous_polyposis_2|Breast_carcinoma": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Familial_colorectal_cancer": 1,
    "Hereditary_spastic_paraplegia_7": 522,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Gastric_cancer|not_specified": 2,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 2,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2|Carcinoma_of_colon": 4,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_specified|not_provided": 1,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Carcinoma_of_colon|Familial_adenomatous_polyposis_2": 1,
    "not_provided|not_specified|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|MUTYH-related_disorder": 3,
    "not_provided|not_specified|Familial_adenomatous_polyposis_2": 1,
    "Familial_colorectal_cancer_type_X|not_specified|Familial_adenomatous_polyposis_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_provided|MUTYH-related_disorder": 1,
    "Familial_adenomatous_polyposis_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Pilomatrixoma|Neoplasm_of_stomach|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 3,
    "not_specified|Familial_adenomatous_polyposis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|MUTYH-related_disorder": 1,
    "not_specified|MUTYH-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_adenomatous_polyposis_2|not_provided": 1,
    "MUTYH-related_disorder|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Colon_cancer": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Pilomatrixoma|Neoplasm_of_stomach|not_specified|not_provided": 1,
    "Familial_colorectal_cancer_type_X|Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Carcinoma_of_colon|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Familial_adenomatous_polyposis_2|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Familial_colorectal_cancer_type_X": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Familial_adenomatous_polyposis_2": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|not_provided|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Familial_adenomatous_polyposis_2": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 2,
    "Familial_adenomatous_polyposis_2|Gastric_cancer": 6,
    "Familial_adenomatous_polyposis_2|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "MUTYH-related_disorder|not_provided|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Familial_adenomatous_polyposis_2": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Pilomatrixoma": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|MUTYH-related_disorder|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Pilomatrixoma|Neoplasm_of_stomach|not_provided|Carcinoma_of_colon|Breast_carcinoma": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|MUTYH-related_disorder|Familial_adenomatous_polyposis_2|not_provided": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_2|Gastric_cancer": 1,
    "not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_provided": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Familial_adenomatous_polyposis_2|Gastric_cancer|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_2|MUTYH-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2": 1,
    "MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_provided|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_specified|not_provided|MUTYH-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Pilomatrixoma|Neoplasm_of_stomach|Familial_adenomatous_polyposis_2|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2|Colon_cancer": 1,
    "MUTYH-related_disorder|Gastric_cancer|Familial_adenomatous_polyposis_2|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Pilomatrixoma|Familial_adenomatous_polyposis_2": 1,
    "Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Familial_adenomatous_polyposis_2|Gastric_cancer|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "not_provided|Familial_adenomatous_polyposis_2|MUTYH-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MUTYH-related_disorder|not_specified": 1,
    "Colonic_neoplasm|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MUTYH-related_disorder|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MUTYH-related_disorder|Familial_adenomatous_polyposis_2|not_specified": 1,
    "MUTYH-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 1,
    "not_provided|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma": 1,
    "not_provided|Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "MUTYH-related_disorder|Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_2|not_provided|MUTYH-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neoplasm_of_stomach|Pilomatrixoma|Familial_adenomatous_polyposis_2|not_provided|Carcinoma_of_colon": 1,
    "not_provided|not_specified|Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "MUTYH-related_disorder|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_specified|Familial_adenomatous_polyposis_2": 1,
    "Familial_adenomatous_polyposis_2|Familial_cancer_of_breast": 2,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|Pilomatrixoma|Neoplasm_of_stomach|not_specified|not_provided": 1,
    "not_provided|not_specified|Carcinoma_of_colon|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2|Carcinoma_of_colon|Gastric_cancer": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|not_provided|Familial_adenomatous_polyposis_2|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_2": 1,
    "MUTYH-related_Breast_Cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_2|Gastric_cancer|not_provided": 1,
    "Familial_colorectal_cancer_type_X|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_adenomatous_polyposis_2|not_specified": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|MUTYH-related_disorder": 1,
    "not_provided|Familial_adenomatous_polyposis_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MUTYH-related_disorder|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Familial_adenomatous_polyposis_2|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|not_provided|MUTYH-related_disorder": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|Pilomatrixoma|Neoplasm_of_stomach|not_provided|Carcinoma_of_colon": 1,
    "not_specified|Carcinoma_of_colon|not_provided|Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_2|MUTYH-related_disorder": 1,
    "Carcinoma_of_colon|not_specified|Familial_adenomatous_polyposis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Pontocerebellar_hypoplasia_type_7|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Carcinoma_of_colon|Familial_adenomatous_polyposis_2": 1,
    "Familial_adenomatous_polyposis_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|not_specified|MUTYH-related_disorder": 1,
    "Familial_adenomatous_polyposis_2|Gastric_cancer|MUTYH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_2|Gastric_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 82,
    "Pontocerebellar_hypoplasia_type_7": 24,
    "TOE1-related_disorder|not_provided": 6,
    "not_specified|not_provided|TOE1-related_disorder": 2,
    "not_provided|Pontocerebellar_hypoplasia_type_7|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_7|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|TOE1-related_disorder": 1,
    "TOE1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TOE1-related_disorder": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_7": 2,
    "Pontocerebellar_hypoplasia_type_7|not_provided": 2,
    "Pontocerebellar_hypoplasia_type_7|TOE1-related_disorder": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_7": 1,
    "not_specified|not_provided|TOE1-related_disorder|Pontocerebellar_hypoplasia_type_7": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism": 256,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Cobalamin_C_disease": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|Cobalamin_C_disease|not_provided": 3,
    "Cobalamin_C_disease": 416,
    "Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC": 5,
    "not_provided|Cobalamin_C_disease": 13,
    "Cobalamin_C_disease|Inborn_genetic_diseases": 5,
    "Cobalamin_C_disease|MMACHC-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|Cobalamin_C_disease": 5,
    "METHYLMALONIC_ACIDURIA_AND_HOMOCYSTINURIA|_cblC_TYPE|_DIGENIC": 2,
    "Cobalamin_C_disease|not_provided": 13,
    "MMACHC-related_disorder|Cobalamin_C_disease|not_specified|not_provided|Methylmalonic_acidemia_with_homocystinuria_cblC": 1,
    "Inborn_genetic_diseases|Cobalamin_C_disease": 4,
    "MMACHC-related_disorder": 1,
    "not_specified|Cobalamin_C_disease|METHYLMALONIC_ACIDURIA_AND_HOMOCYSTINURIA|_cblC_TYPE|_DIGENIC": 1,
    "not_specified|Cobalamin_C_disease": 2,
    "Cobalamin_C_disease|not_specified": 3,
    "Cobalamin_C_disease|not_provided|Inborn_genetic_diseases": 2,
    "Cobalamin_C_disease|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 2,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|Methylmalonic_aciduria|_type_cblc|MMACHC-related_disorder|Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Cobalamin_C_disease": 1,
    "Cobalamin_C_disease|See_cases": 1,
    "Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC|not_provided": 3,
    "Cobalamin_C_disease|Inborn_genetic_diseases|not_provided": 2,
    "METHYLMALONIC_ACIDURIA_AND_HOMOCYSTINURIA|_cblC_TYPE|_DIGENIC|Methylmalonic_acidemia_with_homocystinuria_cblC|Methylmalonic_aciduria_and_homocystinuria|MMACHC-related_disorder|Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Cobalamin_C_disease|See_cases": 1,
    "Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|Inborn_genetic_diseases": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Cobalamin_C_disease": 1,
    "not_provided|Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC": 4,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Cobalamin_C_disease|not_specified": 1,
    "Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC": 1,
    "MMACHC-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_acidemia_with_homocystinuria_cblC|not_provided|Cobalamin_C_disease": 1,
    "not_specified|not_provided|MMACHC-related_disorder|Methylmalonic_acidemia_with_homocystinuria_cblC|Cobalamin_C_disease": 1,
    "Inborn_genetic_diseases|Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism": 5,
    "not_specified|not_provided|Cobalamin_C_disease": 1,
    "Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism": 3,
    "not_provided|Cobalamin_C_disease|not_specified": 1,
    "Cobalamin_C_disease|MMACHC-related_disorder|not_provided": 1,
    "Cobalamin_C_disease|MMACHC-related_disorder|Retinal_dystrophy|not_provided": 1,
    "cblC_type_of_combined_methylmalonic_aciduria_and_homocystinuria|Methylmalonic_acidemia_with_homocystinuria_cblC|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Cobalamin_C_disease|Methylmalonic_aciduria_and_homocystinuria_type_cblD|Abnormality_of_metabolism/homeostasis": 1,
    "Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC|MMACHC-related_disorder|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Cobalamin_C_disease": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|MMACHC-related_disorder|Methylmalonic_aciduria|Homocystinuria|Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Cobalamin_C_disease": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|MMACHC-related_disorder|Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "MMACHC-related_disorder|Methylmalonic_acidemia_with_homocystinuria_cblC|Cobalamin_C_disease": 1,
    "Inborn_genetic_diseases|Cobalamin_C_disease|See_cases|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|not_specified|Cobalamin_C_disease": 1,
    "MMACHC-related_disorder|Methylmalonic_acidemia_with_homocystinuria_cblC|not_provided|Cobalamin_C_disease": 2,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|MMACHC-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|Inborn_genetic_diseases|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Cobalamin_C_disease": 1,
    "Cobalamin_C_disease|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC": 2,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria_cblC|Inborn_genetic_diseases|Cobalamin_C_disease": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|not_provided|Cobalamin_C_disease": 2,
    "not_provided|Cobalamin_C_disease|Inborn_genetic_diseases": 2,
    "Cobalamin_C_disease|not_provided|Methylmalonic_acidemia_with_homocystinuria_cblC": 2,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Cobalamin_C_disease": 1,
    "Inborn_genetic_diseases|Cobalamin_C_disease|not_provided|not_specified": 1,
    "not_provided|Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism": 3,
    "Inborn_genetic_diseases|Cobalamin_C_disease|not_provided": 2,
    "not_specified|not_provided|Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC": 1,
    "Cobalamin_C_disease|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "MMACHC-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Cobalamin_C_disease": 1,
    "Inborn_genetic_diseases|not_specified|Cobalamin_C_disease": 1,
    "Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria_cblC|MMACHC-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria_cblC|not_specified|Inborn_genetic_diseases|Cobalamin_C_disease": 1,
    "not_provided|Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 1,
    "not_specified|Methylmalonic_acidemia_with_homocystinuria_cblC|Cobalamin_C_disease|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylmalonic_acidemia_with_homocystinuria_cblC|MMACHC-related_disorder|not_specified|not_provided|Cobalamin_C_disease": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 33,
    "not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism": 28,
    "METHYLMALONIC_ACIDURIA_AND_HOMOCYSTINURIA|_cblC_TYPE|_DIGENIC|not_provided|Cobalamin_C_disease": 1,
    "PRDX1-related_disorder|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 74,
    "Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided": 1,
    "POMGNT1-related_disorder": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 5,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|POMGNT1-related_disorder": 1,
    "not_provided|Muscle_eye_brain_disease": 2,
    "Muscle_eye_brain_disease": 46,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 730,
    "Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided": 6,
    "Optic_atrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|POMGNT1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 55,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided|Muscle_eye_brain_disease|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided": 27,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscle_eye_brain_disease": 6,
    "Muscle_eye_brain_disease|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_specified|Retinitis_pigmentosa_76|not_provided": 1,
    "not_provided|Myopathy_caused_by_variation_in_POMGNT1|POMGNT1-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|not_provided|Muscle_eye_brain_disease": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Retinal_dystrophy|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Inborn_genetic_diseases": 2,
    "Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 11,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 23,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 15,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|not_specified|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 7,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 6,
    "Phenylketonuria": 927,
    "Abnormality_of_the_nervous_system": 41,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 8,
    "POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Inborn_genetic_diseases": 1,
    "not_provided|Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 2,
    "Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|not_provided|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76": 1,
    "not_specified|Muscle_eye_brain_disease|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided": 6,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Inborn_genetic_diseases|Muscle_eye_brain_disease": 2,
    "Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 2,
    "Retinal_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 5,
    "Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided": 2,
    "Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Muscle_eye_brain_disease": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 6,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76": 1,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 5,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Structural_eye_disease|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscle_eye_brain_disease": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 3,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "not_specified|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|POMGNT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 4,
    "POMGNT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinal_dystrophy|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified": 8,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Myopathy_caused_by_variation_in_POMGNT1|POMGNT1-related_disorder|Muscle_eye_brain_disease|Congenital_muscular_alpha-dystroglycanopathy_with_brain_and_eye_anomalies|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy|Retinal_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinal_dystrophy": 3,
    "Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Retinal_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|POMGNT1-related_disorder": 1,
    "Retinitis_pigmentosa_76": 4,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|POMGNT1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|Retinal_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy|Retinal_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|POMGNT1-related_disorder|Muscular_dystrophy-dystroglycanopathy|not_provided|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy|not_provided": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy": 1,
    "Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Inborn_genetic_diseases|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinal_dystrophy|not_provided|Muscle_eye_brain_disease": 1,
    "not_provided|not_specified|Retinal_dystrophy|Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Inborn_genetic_diseases": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease|POMGNT1-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|Retinal_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|POMGNT1-related_disorder|Muscular_dystrophy-dystroglycanopathy": 1,
    "Retinitis_pigmentosa_76|POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|Muscle_eye_brain_disease": 1,
    "Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|Retinitis_pigmentosa_76": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|not_provided|POMGNT1-related_disorder|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|not_specified|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Retinitis_pigmentosa_76": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided": 2,
    "Limb-girdle_muscular_dystrophy": 15,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Inborn_genetic_diseases|not_provided|Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified": 1,
    "Hypotonia": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinal_dystrophy|Muscle_eye_brain_disease": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|not_specified|not_provided": 2,
    "POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|POMGNT1-related_disorder|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Intellectual_disability": 1,
    "Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 1,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_specified|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinitis_pigmentosa": 1,
    "Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinal_dystrophy|Muscle_eye_brain_disease": 1,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Inborn_genetic_diseases|Retinal_dystrophy|Muscular_dystrophy-dystroglycanopathy|not_provided": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 2,
    "Muscular_dystrophy-dystroglycanopathy|Muscle_eye_brain_disease": 3,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 2,
    "Myopathy_caused_by_variation_in_POMGNT1": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscle_eye_brain_disease": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinitis_pigmentosa_76": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscle_eye_brain_disease|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|Retinal_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease|POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|POMGNT1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy|not_provided": 1,
    "Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "POMGNT1-related_disorder|Retinitis_pigmentosa_76|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_specified|not_provided": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinal_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Muscle_eye_brain_disease": 1,
    "Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 2,
    "Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Retinitis_pigmentosa_76": 1,
    "not_provided|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 3,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinal_dystrophy|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy": 4,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Retinitis_pigmentosa_76|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Retinal_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|not_provided|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 2,
    "Muscle_eye_brain_disease|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy|Retinal_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|Retinitis_pigmentosa|Muscle_eye_brain_disease|not_provided": 1,
    "POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "not_specified|POMGNT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|not_provided|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinal_dystrophy|not_specified": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinal_dystrophy|Retinitis_pigmentosa|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscle_eye_brain_disease|Retinitis_pigmentosa_76|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|POMGNT1-related_disorder|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|not_provided|Muscle_eye_brain_disease": 1,
    "Retinal_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|POMGNT1-related_disorder": 1,
    "not_specified|Muscle_eye_brain_disease|not_provided": 1,
    "not_provided|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy": 1,
    "Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided|Muscular_dystrophy-dystroglycanopathy|Retinitis_pigmentosa_76": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "Inborn_genetic_diseases|not_provided|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscle_eye_brain_disease": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscular_dystrophy-dystroglycanopathy|not_provided|Muscle_eye_brain_disease": 1,
    "Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 1,
    "Retinitis_pigmentosa_76|Muscle_eye_brain_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|POMGNT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|not_specified|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_provided|Muscle_eye_brain_disease|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease|Inborn_genetic_diseases": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease|Retinitis_pigmentosa_76": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|Inborn_genetic_diseases": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Retinal_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease": 1,
    "Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|not_provided": 1,
    "Retinal_dystrophy|Muscle_eye_brain_disease|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|not_provided|Muscle_eye_brain_disease": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Retinitis_pigmentosa_76|Muscle_eye_brain_disease": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Inborn_genetic_diseases": 1,
    "Hydrocephalus|Abnormality_of_the_nervous_system": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Muscle_eye_brain_disease|not_provided": 1,
    "not_provided|Muscle_eye_brain_disease|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Retinal_dystrophy|not_specified": 1,
    "not_provided|Muscle_eye_brain_disease|Inborn_genetic_diseases": 1,
    "Muscle_eye_brain_disease|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2O": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 9,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome": 116,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 15,
    "RAD54L-related_disorder|not_specified": 1,
    "Astrocytoma_IDH-mutant": 1,
    "Colon_adenocarcinoma": 1,
    "Lymphoma|_non-Hodgkin|_familial": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome": 180,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified": 99,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 8,
    "not_specified|RAD54L-related_disorder": 3,
    "RAD54L-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|RAD54L-related_disorder|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided": 151,
    "not_specified|Non-Hodgkin_lymphoma": 1,
    "Non-Hodgkin_lymphoma|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Premature_ovarian_failure": 1,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|RAD54L-related_disorder|not_specified": 3,
    "not_specified|Familial_cancer_of_breast": 57,
    "Non-Hodgkin_lymphoma": 4,
    "RAD54L-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|not_specified": 66,
    "Autosomal_dominant_hypophosphatemic_rickets": 3,
    "Mitochondrial_complex_III_deficiency|_nuclear_type_11": 2,
    "FAAH-related_disorder": 3,
    "Polysubstance_abuse|_susceptibility_to|FAAH-related_disorder|not_provided|FAAH_POLYMORPHISM": 1,
    "Polysubstance_abuse|_susceptibility_to": 1,
    "Global_developmental_delay|Seizure|Hearing_impairment|Hypotonia|Strabismus|Hypermetropia": 1,
    "DMBX1-related_disorder": 6,
    "not_specified|DMBX1-related_disorder": 1,
    "Pulmonary_disease|_chronic_obstructive|_susceptibility_to": 27,
    "TAL1-related_disorder": 7,
    "not_specified|TAL1-related_disorder": 2,
    "Microcephaly_7|_primary|_autosomal_recessive": 71,
    "Primary_Microcephaly|_Recessive": 11,
    "not_provided|Microcephaly_7|_primary|_autosomal_recessive": 14,
    "Microcephaly_7|_primary|_autosomal_recessive|not_provided": 8,
    "Microcephaly_7|_primary|_autosomal_recessive|not_specified|not_provided": 3,
    "Microcephaly_7|_primary|_autosomal_recessive|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_7|_primary|_autosomal_recessive": 1,
    "STIL-related_disorder|not_specified|not_provided|Microcephaly_7|_primary|_autosomal_recessive": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|Microcephaly_7|_primary|_autosomal_recessive": 1,
    "STIL-related_disorder|not_provided|Microcephaly_7|_primary|_autosomal_recessive": 1,
    "Microcephaly_7|_primary|_autosomal_recessive|not_provided|not_specified": 2,
    "not_specified|not_provided|Microcephaly_7|_primary|_autosomal_recessive": 5,
    "not_provided|STIL-related_disorder": 4,
    "Inborn_genetic_diseases|Microcephaly_7|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|not_specified|Microcephaly_7|_primary|_autosomal_recessive": 1,
    "Neutrophil_inclusion_bodies": 2,
    "Microcephaly_7|_primary|_autosomal_recessive|STIL-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Microcephaly_7|_primary|_autosomal_recessive": 1,
    "Microcephaly_7|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly_7|_primary|_autosomal_recessive|STIL-related_disorder": 1,
    "Inborn_genetic_diseases|Microcephaly_7|_primary|_autosomal_recessive": 3,
    "STIL-related_disorder": 3,
    "Microcephaly_7|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Microcephaly_7|_primary|_autosomal_recessive|Abnormal_brain_morphology": 1,
    "not_specified|Microcephaly_7|_primary|_autosomal_recessive|not_provided": 1,
    "Microcephaly_7|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Microcephaly_7|_primary|_autosomal_recessive": 1,
    "STIL-related_disorder|not_specified|not_provided": 1,
    "Microcephaly_7|_primary|_autosomal_recessive|not_provided|STIL-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly_7|_primary|_autosomal_recessive|not_specified": 1,
    "not_provided|Microcephaly_7|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia": 75,
    "FOXE3-related_disorder": 8,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to|not_specified": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype": 23,
    "Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia": 52,
    "Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia|not_specified|not_provided": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis": 73,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|Cardiovascular_phenotype": 22,
    "Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis": 26,
    "not_specified|Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia|not_provided": 2,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype|not_provided": 3,
    "not_specified|Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis": 2,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|not_provided": 2,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|FOXE3-related_disorder": 3,
    "Cardiovascular_phenotype|not_provided|Anterior_segment_dysgenesis_1|Anterior_segment_dysgenesis|Congenital_primary_aphakia|not_specified": 1,
    "Congenital_primary_aphakia": 12,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_provided|Cardiovascular_phenotype": 1,
    "FOXE3-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Congenital_primary_aphakia|Anterior_segment_dysgenesis": 4,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|FOXE3-related_disorder": 1,
    "FOXE3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype|not_specified": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype|FOXE3-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis|FOXE3-related_disorder|Cataract_34_multiple_types|not_provided": 1,
    "not_specified|Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype|not_provided": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_provided": 4,
    "Cataract_34_multiple_types": 3,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_provided|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Cardiovascular_phenotype": 1,
    "Cataract_34_multiple_types|Congenital_primary_aphakia|Anterior_segment_dysgenesis": 1,
    "Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to|Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia": 1,
    "Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis|FOXE3-related_disorder": 1,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Congenital_primary_aphakia|Anterior_segment_dysgenesis|Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to": 1,
    "FOXE3-related_disorder|Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_specified": 1,
    "not_provided|Anterior_segment_dysgenesis|Congenital_primary_aphakia": 1,
    "Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection|Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis|Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Cardiovascular_phenotype": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_provided|Cardiovascular_phenotype": 1,
    "Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta": 2,
    "Cataract_34_multiple_types|Congenital_primary_aphakia|Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to|Anterior_segment_dysgenesis|Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FOXE3-related_disorder|Cardiovascular_phenotype|not_provided|Anterior_segment_dysgenesis|Congenital_primary_aphakia": 1,
    "Cardiovascular_phenotype|FOXE3-related_disorder|not_provided|Congenital_primary_aphakia|Anterior_segment_dysgenesis": 1,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Anterior_segment_dysgenesis_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia|FOXE3-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_primary_aphakia|Anterior_segment_dysgenesis|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_provided|Cardiovascular_phenotype": 1,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Congenital_primary_aphakia|Anterior_segment_dysgenesis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|Aortic_aneurysm|_familial_thoracic_11|_susceptibility_to": 1,
    "Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis|not_provided": 1,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Anterior_segment_dysgenesis|not_provided|Congenital_primary_aphakia": 1,
    "not_provided|Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia": 1,
    "FOXE3-related_disorder|Cardiovascular_phenotype|Congenital_primary_aphakia|Anterior_segment_dysgenesis": 1,
    "Anterior_segment_dysgenesis|Congenital_primary_aphakia|Cardiovascular_phenotype|not_provided": 1,
    "FOXE3-related_disorder|Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia": 2,
    "Cardiovascular_phenotype|Anterior_segment_dysgenesis|Congenital_primary_aphakia|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FOXD2-associated_disorder": 1,
    "SLC5A9-related_disorder": 25,
    "not_provided|SLC5A9-related_disorder": 1,
    "AGBL4-related_disorder": 10,
    "Multiple_myeloma": 42,
    "Infantile_epilepsy_syndrome": 9,
    "Meier-Gorlin_syndrome_1": 30,
    "not_provided|Meier-Gorlin_syndrome_1": 8,
    "not_provided|ORC1-related_disorder|Meier-Gorlin_syndrome_1": 3,
    "Inborn_genetic_diseases|Meier-Gorlin_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Meier-Gorlin_syndrome_1": 2,
    "Meier-Gorlin_syndrome_1|not_provided": 11,
    "ORC1-related_disorder|not_provided": 3,
    "not_provided|Meier-Gorlin_syndrome_1|not_specified": 2,
    "Meier-Gorlin_syndrome_1|Inborn_genetic_diseases": 3,
    "Meier-Gorlin_syndrome_1|not_specified|not_provided": 3,
    "ORC1-related_disorder|not_provided|Meier-Gorlin_syndrome_1|not_specified": 1,
    "not_specified|Meier-Gorlin_syndrome_1|not_provided": 4,
    "Inborn_genetic_diseases|ORC1-related_disorder": 1,
    "ORC1-related_disorder|Meier-Gorlin_syndrome_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Meier-Gorlin_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Meier-Gorlin_syndrome_1|Inborn_genetic_diseases": 1,
    "Meier-Gorlin_syndrome_1|not_provided|Inborn_genetic_diseases": 2,
    "ORC1-related_disorder|not_specified|not_provided|Meier-Gorlin_syndrome_1": 2,
    "not_provided|ORC1-related_disorder": 1,
    "not_provided|not_specified|Meier-Gorlin_syndrome_1": 1,
    "Meier-Gorlin_syndrome_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Meier-Gorlin_syndrome_1": 1,
    "Meier-Gorlin_syndrome_1|not_specified": 1,
    "ORC1-related_disorder|Meier-Gorlin_syndrome|Inborn_genetic_diseases|not_provided|Meier-Gorlin_syndrome_1": 1,
    "ORC1-related_disorder|not_provided|Meier-Gorlin_syndrome_1": 1,
    "Meier-Gorlin_syndrome_1|ORC1-related_disorder|not_provided": 1,
    "ORC1-related_disorder|Meier-Gorlin_syndrome_1|not_provided|not_specified": 1,
    "Meier-Gorlin_syndrome": 18,
    "COA7-related_disorder|not_provided": 3,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_3": 6,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_3|not_provided": 1,
    "COA7-related_disorder": 1,
    "Craniofacial_microsomia_1": 12,
    "ZYG11B-related_disorder": 1,
    "SCP2-related_disorder|not_provided": 10,
    "not_provided|SCP2-related_disorder": 6,
    "Sterol_carrier_protein_2_deficiency|not_provided": 3,
    "SCP2-related_disorder": 2,
    "Leukodystrophy": 5,
    "Sterol_carrier_protein_2_deficiency|not_provided|not_specified": 1,
    "not_specified|not_provided|SCP2-related_disorder": 1,
    "not_provided|Sterol_carrier_protein_2_deficiency": 3,
    "Sterol_carrier_protein_2_deficiency": 4,
    "Sensorineural_hearing_loss_disorder|not_provided": 7,
    "SCP2-related_disorder|not_specified|not_provided": 2,
    "not_provided|SCP2-related_disorder|Sterol_carrier_protein_2_deficiency": 1,
    "not_specified|SCP2-related_disorder|not_provided": 1,
    "SCP2-related_disorder|not_provided|not_specified": 1,
    "SCP2-related_disorder|not_provided|Sterol_carrier_protein_2_deficiency": 1,
    "Carnitine_palmitoyltransferase_II_deficiency": 684,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "not_provided|Carnitine_palmitoyltransferase_II_deficiency": 10,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency": 4,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 16,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 4,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 21,
    "Carnitine_palmitoyltransferase_II_deficiency|not_specified": 6,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 16,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 2,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "not_specified|Carnitine_palmitoyltransferase_II_deficiency": 5,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 4,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 19,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided": 2,
    "Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 2,
    "not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 4,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 4,
    "not_provided|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 5,
    "Inborn_genetic_diseases|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Genu_valgum|Hyperextensibility_at_elbow|Myopathic_facies|Hyperextensible_hand_joints|Hyperextensibility_of_the_finger_joints|Generalized_hypotonia|Pes_planus|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 7,
    "Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "not_specified|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Rhabdomyolysis|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided|Abnormality_of_the_musculature": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 2,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency": 5,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 2,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_specified": 1,
    "not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided": 5,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 3,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|CPT2-related_disorder|not_specified": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency": 9,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 2,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 6,
    "Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases": 5,
    "not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided|CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_specified|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 3,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 2,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "CPT2-related_disorder": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_specified|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "not_provided|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided|CPT2-related_disorder": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 3,
    "Microcephaly|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 3,
    "Inborn_genetic_diseases|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_specified|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided": 1,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "not_specified|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Inborn_genetic_diseases|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_specified": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_specified|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_specified|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "not_specified|Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 2,
    "not_provided|not_specified|CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 2,
    "CPT2-related_disorder|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 2,
    "Inborn_genetic_diseases|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "CPT2-related_disorder|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_specified": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency": 3,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Abnormality_of_the_nervous_system|Seizure": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Inborn_genetic_diseases|not_specified|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 2,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided": 1,
    "not_specified|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|not_specified|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 2,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|CPT2-related_disorder|Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|CPT2-related_disorder": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|Pes_planus|Hyperextensibility_at_elbow|Generalized_hypotonia|Myopathic_facies|Hyperextensible_hand_joints|Hyperextensibility_of_the_finger_joints|Genu_valgum|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_provided|Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency|not_specified": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Inborn_genetic_diseases|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency": 3,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_specified": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency": 2,
    "CPT2-related_disorder|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|CPT2-related_disorder|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_specified|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_specified": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_specified|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|not_specified": 1,
    "not_specified|CPT2-related_disorder|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Inborn_genetic_diseases|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|CPT2-related_disorder|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "not_provided|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|CPT2-related_disorder|not_specified|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Myopathy|Rhabdomyolysis|Kidney_damage|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_specified|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|See_cases": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_specified|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "not_specified|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|not_provided": 1,
    "not_specified|not_provided|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form": 1,
    "CPT2-related_disorder|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|not_provided|Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyltransferase_II_deficiency|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|CPT2-related_disorder": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Carnitine_palmitoyltransferase_II_deficiency|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Carnitine_palmitoyltransferase_II_deficiency|not_provided": 1,
    "Carnitine_palmitoyl_transferase_II_deficiency|_severe_infantile_form|Carnitine_palmitoyl_transferase_II_deficiency|_neonatal_form|Carnitine_palmitoyl_transferase_II_deficiency|_myopathic_form|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_4|Inborn_genetic_diseases|not_specified|Carnitine_palmitoyltransferase_II_deficiency": 1,
    "Myocardial_infarction|_susceptibility_to|_1": 3,
    "Myocardial_infarction|_susceptibility_to": 6,
    "LRP8-related_disorder": 6,
    "LRP8-related_disorder|not_provided": 2,
    "not_provided|LRP8-related_disorder": 1,
    "Hereditary_coproporphyria|NEURODEVELOPMENTAL_DISORDER_WITH_ACHALASIA|_POLYNEUROPATHY|_AND_ALACRIMA": 2,
    "Global_developmental_delay|Retinal_disorder|Cleft_palate": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_ACHALASIA|_POLYNEUROPATHY|_AND_ALACRIMA": 1,
    "Hereditary_coproporphyria": 49,
    "Thyroid_hormone_metabolism|_abnormal|_2": 2,
    "Levothyroxine_response": 6,
    "Renal_agenesis": 5,
    "Estrogen_resistance_syndrome": 12,
    "Syndromic_intellectual_disability": 39,
    "Developmental_and_epileptic_encephalopathy|_75": 11,
    "PARS2-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_75|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_75|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_75|PARS2-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_75|Inborn_genetic_diseases|not_provided": 1,
    "PARS2-related_disorder|not_specified|not_provided": 1,
    "not_provided|PARS2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_75": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_75": 1,
    "Developmental_and_epileptic_encephalopathy|_75|PARS2-related_disorder|not_provided": 1,
    "not_provided|not_specified|PARS2-related_disorder": 1,
    "not_provided|Desmosterolosis": 17,
    "Desmosterolosis": 70,
    "Desmosterolosis|not_provided": 9,
    "not_specified|Desmosterolosis": 2,
    "not_provided|Desmosterolosis|not_specified": 1,
    "Inborn_genetic_diseases|Desmosterolosis|not_provided": 1,
    "not_provided|not_specified|Desmosterolosis": 1,
    "not_provided|Non-immune_hydrops_fetalis": 5,
    "Non-immune_hydrops_fetalis|Desmosterolosis": 1,
    "DHCR24-related_disorder|not_provided": 2,
    "Desmosterolosis|not_specified|not_provided": 1,
    "not_provided|DHCR24-related_disorder": 1,
    "Schizophrenia": 105,
    "not_provided|Inborn_genetic_diseases|Desmosterolosis": 1,
    "not_specified|Desmosterolosis|not_provided|Inborn_genetic_diseases": 1,
    "Desmosterolosis|not_provided|DHCR24-related_disorder": 1,
    "DHCR24-related_disorder|Desmosterolosis": 1,
    "Desmosterolosis|Inborn_genetic_diseases": 1,
    "Desmosterolosis|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Desmosterolosis|DHCR24-related_disorder": 1,
    "not_specified|Desmosterolosis|not_provided": 1,
    "not_provided|Bartter_disease_type_4A": 10,
    "Bartter_disease_type_4A": 12,
    "Bartter_disease_type_4A|not_provided": 14,
    "not_specified|Bartter_disease_type_4A": 1,
    "Bartter_disease_type_4A|Bartter_syndrome|not_provided": 4,
    "Bartter_disease_type_4A|Bartter_syndrome|not_specified|not_provided": 1,
    "not_provided|Bartter_syndrome|not_specified|Bartter_disease_type_4A": 1,
    "Hearing_impairment|not_provided|Sensorineural_deafness_with_mild_renal_dysfunction|Bartter_disease_type_4A": 1,
    "Bartter_disease_type_4A|Bartter_syndrome|BSND-related_disorder|not_provided": 1,
    "not_specified|not_provided|Bartter_syndrome_type_4|Bartter_disease_type_4A": 1,
    "not_provided|Bartter_syndrome": 7,
    "not_provided|Hearing_loss|_autosomal_recessive|Sensorineural_deafness_with_mild_renal_dysfunction|Bartter_disease_type_4A|Bartter_syndrome": 1,
    "not_specified|Bartter_syndrome|not_provided|Bartter_disease_type_4A": 1,
    "Inborn_genetic_diseases|Bartter_disease_type_4A": 1,
    "Bartter_syndrome|not_provided|BSND-related_disorder": 2,
    "Bartter_syndrome|Bartter_disease_type_4A": 1,
    "not_provided|not_specified|Bartter_disease_type_4A|Bartter_syndrome": 1,
    "Bartter_syndrome|not_provided": 6,
    "not_provided|Bartter_disease_type_4A|Bartter_syndrome|not_specified": 1,
    "Bartter_syndrome_type_4|Bartter_disease_type_4A|not_provided|Bartter_syndrome|BSND-related_disorder|Hearing_loss|_autosomal_recessive": 1,
    "BSND-related_disorder|Bartter_syndrome|not_provided": 1,
    "not_provided|Bartter_disease_type_4A|not_specified": 2,
    "Bartter_disease_type_4A|not_provided|not_specified": 1,
    "not_provided|not_specified|Bartter_syndrome|Bartter_disease_type_4A": 1,
    "Bartter_syndrome|not_provided|Bartter_disease_type_4A": 2,
    "Bartter_syndrome|not_specified|not_provided|Bartter_disease_type_4A": 2,
    "Bartter_syndrome|Bartter_disease_type_4A|not_provided": 3,
    "not_specified|Bartter_syndrome|Inborn_genetic_diseases|Bartter_disease_type_4A": 1,
    "Inborn_genetic_diseases|Bartter_syndrome|not_specified|not_provided|Bartter_disease_type_4A": 1,
    "Bartter_disease_type_4A|not_specified|Bartter_syndrome|not_provided": 1,
    "not_specified|Bartter_syndrome": 1,
    "not_provided|Bartter_disease_type_4A|Inborn_genetic_diseases|not_specified": 1,
    "BSND-related_disorder|not_specified|not_provided|Bartter_disease_type_4A": 1,
    "Bartter_disease_type_4A|not_specified": 1,
    "Bartter_disease_type_4A|not_provided|Inborn_genetic_diseases": 1,
    "BSND-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Bartter_syndrome": 1,
    "BSND-related_disorder|not_provided": 2,
    "not_provided|not_specified|Bartter_disease_type_4A": 1,
    "not_specified|Bartter_disease_type_4A|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_4A": 1,
    "not_provided|Bartter_disease_type_4A|Bartter_syndrome": 1,
    "not_specified|Bartter_disease_type_4A|not_provided|Bartter_syndrome": 1,
    "not_specified|not_provided|Bartter_disease_type_4A": 1,
    "Bartter_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Bartter_disease_type_4A|Inborn_genetic_diseases|Bartter_syndrome|not_provided": 1,
    "Bartter_disease_type_4A|not_provided|Bartter_syndrome|not_specified": 1,
    "not_provided|Bartter_syndrome|Bartter_disease_type_4A": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_4A|not_specified": 1,
    "not_specified|not_provided|Bartter_disease_type_4A|Bartter_syndrome": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 5,
    "Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1": 19,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 19,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1|Hypobetalipoproteinemia": 2,
    "Hypercholesterolemia|_autosomal_dominant|_3|Hypobetalipoproteinemia": 11,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3": 350,
    "Familial_hypercholesterolemia|PCSK9-related_disorder|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 134,
    "Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia": 10,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 44,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified": 1,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 8,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 25,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 10,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 62,
    "not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 2,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 4,
    "PCSK9-related_disorder|Hypercholesterolemia|_familial|_1|not_specified|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 9,
    "PCSK9-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_1|not_specified|Cardiovascular_phenotype": 2,
    "Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 32,
    "not_specified|Hypercholesterolemia|_familial|_1": 7,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "PCSK9-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypobetalipoproteinemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "not_provided|PCSK9-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 5,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 4,
    "not_provided|Familial_hypercholesterolemia": 10,
    "Cardiovascular_phenotype|Hypocholesterolemia|Hypobetalipoproteinemia|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Low_density_lipoprotein_cholesterol_level_quantitative_trait_locus_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_specified|Hypobetalipoproteinemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 4,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 3,
    "Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "PCSK9-related_disorder": 1,
    "not_provided|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Cardiovascular_phenotype|Hypocholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_familial|_1|not_provided": 53,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 4,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|not_specified|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 13,
    "Familial_hypercholesterolemia|not_provided": 31,
    "not_specified|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_3|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Low_density_lipoprotein_cholesterol_level_quantitative_trait_locus_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|not_provided|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|PCSK9-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 4,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 6,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|Hypobetalipoproteinemia": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "not_provided|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 2,
    "Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Familial_hypercholesterolemia": 2,
    "Hypercholesterolemia|_familial|_1|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 11,
    "PCSK9-related_disorder|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 3,
    "Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Low_density_lipoprotein_cholesterol_level_quantitative_trait_locus_1": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 7,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|not_provided": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 433,
    "High_myopia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|High_myopia": 1,
    "not_specified|Cardiovascular_phenotype|Hypobetalipoproteinemia|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|PCSK9-related_disorder|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Hypobetalipoproteinemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|PCSK9-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypobetalipoproteinemia|not_provided|PCSK9-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 5,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 2,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|Hypobetalipoproteinemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_provided|Hypercholesterolemia|_familial|_1": 46,
    "not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Familial_hypercholesterolemia|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Short_fetal_femur_length|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypocholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|not_specified|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 1,
    "not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypobetalipoproteinemia|PCSK9-related_disorder|Hypercholesterolemia|_autosomal_dominant|_3|not_specified|Short_fetal_femur_length|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|not_specified": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 1,
    "not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Cardiovascular_phenotype|not_specified|Hypobetalipoproteinemia|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|not_provided|not_specified": 1,
    "Familial_hypercholesterolemia|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1|not_specified|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 2,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia": 3,
    "not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Familial_hypercholesterolemia|PCSK9-related_disorder|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|PCSK9-related_disorder|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "PCSK9-related_disorder|Familial_hypercholesterolemia|not_specified|Hypobetalipoproteinemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 3,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia|not_specified": 1,
    "Familial_hypercholesterolemia|PCSK9-related_disorder|Hypobetalipoproteinemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_specified": 11,
    "Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_provided|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_specified": 1,
    "Hypobetalipoproteinemia|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 1,
    "PCSK9-related_disorder|Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_familial|_1|not_provided|Short_fetal_femur_length": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypobetalipoproteinemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "not_specified|Cardiovascular_phenotype|Hypobetalipoproteinemia|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Hypobetalipoproteinemia|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|PCSK9-related_disorder|Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia": 3,
    "Hypercholesterolemia|_autosomal_dominant|_3|PCSK9-related_disorder": 1,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "PCSK9-related_disorder|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_provided|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|See_cases": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 2,
    "PCSK9-related_disorder|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 1,
    "PCSK9-related_disorder|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|not_specified|not_provided": 1,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia|not_provided": 1,
    "Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Hypercholesterolemia|_autosomal_dominant|_3|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype": 96,
    "Cardiovascular_phenotype|PCSK9-related_disorder|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 2,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 8,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_3|Familial_hypercholesterolemia|not_provided": 1,
    "Familial_hypercholesterolemia|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "PCSK9-related_disorder|Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Hypobetalipoproteinemia|not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 1,
    "Hypobetalipoproteinemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|not_specified": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_3|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided|not_specified|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Cardiovascular_phenotype|Hypobetalipoproteinemia|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypobetalipoproteinemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "PCSK9-related_disorder|Cardiovascular_phenotype|Hypocholesterolemia|Familial_hypercholesterolemia|not_specified|not_provided|Low_density_lipoprotein_cholesterol_level_quantitative_trait_locus_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_3": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia": 11,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|not_provided": 2,
    "Hypobetalipoproteinemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_3": 2,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_3|PCSK9-related_disorder": 1,
    "not_provided|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia": 1,
    "PRKAA2-related_disorder": 4,
    "not_provided|PRKAA2-related_disorder": 1,
    "PRKAA2-related_disorder|not_provided": 1,
    "Type_I_complement_component_8_deficiency": 2,
    "not_provided|C8A-related_disorder": 6,
    "not_provided|Type_I_complement_component_8_deficiency": 5,
    "not_specified|not_provided|Type_I_complement_component_8_deficiency": 2,
    "Type_I_complement_component_8_deficiency|not_provided": 2,
    "not_specified|not_provided|COMPLEMENT_COMPONENT_8|_ALPHA_SUBUNIT|_A/B_POLYMORPHISM|Type_I_complement_component_8_deficiency": 1,
    "C8A-related_disorder|not_provided": 5,
    "C8A-related_disorder": 1,
    "C8A-related_disorder|Type_I_complement_component_8_deficiency|not_provided": 1,
    "Type_I_complement_component_8_deficiency|not_provided|C8A-related_disorder": 1,
    "not_provided|C8B-related_disorder": 6,
    "Type_II_complement_component_8_deficiency": 4,
    "not_provided|Type_II_complement_component_8_deficiency": 4,
    "not_specified|not_provided|Type_II_complement_component_8_deficiency": 1,
    "Inborn_genetic_diseases|Type_II_complement_component_8_deficiency|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Type_II_complement_component_8_deficiency": 2,
    "Type_II_complement_component_8_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "C8B-related_disorder": 1,
    "Type_II_complement_component_8_deficiency|not_provided": 8,
    "C8B-related_disorder|Type_II_complement_component_8_deficiency|Complement_component_6_deficiency|not_provided": 1,
    "C8B-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Type_II_complement_component_8_deficiency": 1,
    "Type_II_complement_component_8_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Type_II_complement_component_8_deficiency|not_provided|not_specified": 1,
    "C8B-related_disorder|not_provided|Type_II_complement_component_8_deficiency|Complement_component_6_deficiency": 1,
    "DAB1-related_disorder": 10,
    "Irido-corneo-trabecular_dysgenesis|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|DAB1-related_disorder": 2,
    "not_specified|Spinocerebellar_ataxia_type_37": 3,
    "Spinocerebellar_ataxia_type_37": 3,
    "Corneal_Dystrophy|_Dominant/Recessive|not_provided": 1,
    "not_provided|Gelatinous_droplike_corneal_dystrophy": 12,
    "Corneal_Dystrophy|_Dominant/Recessive": 1,
    "Gelatinous_droplike_corneal_dystrophy": 36,
    "Gelatinous_droplike_corneal_dystrophy|not_provided": 4,
    "not_specified|not_provided|Gelatinous_droplike_corneal_dystrophy": 1,
    "not_specified|Gelatinous_droplike_corneal_dystrophy|not_provided": 1,
    "not_provided|TACSTD2-related_disorder": 1,
    "TACSTD2-related_disorder": 2,
    "Gelatinous_droplike_corneal_dystrophy|not_specified": 1,
    "not_specified|Gelatinous_droplike_corneal_dystrophy": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|MYSM1-related_disorder": 1,
    "not_provided|MYSM1-related_disorder": 7,
    "MYSM1-related_disorder|not_provided": 6,
    "not_provided|Congenital_progressive_bone_marrow_failure-B-cell_immunodeficiency-skeletal_dysplasia_syndrome": 1,
    "not_provided|Bone_marrow_failure_syndrome_4": 9,
    "Bone_marrow_failure_syndrome_4|not_provided": 3,
    "Bone_marrow_failure_syndrome_4": 7,
    "not_provided|MYSM1-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Bone_marrow_failure_syndrome_4": 1,
    "MYSM1-related_disorder": 1,
    "MYSM1-related_disorder|Bone_marrow_failure_syndrome_4|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|MYSM1-related_disorder": 1,
    "Inborn_genetic_diseases|MYSM1-related_disorder|not_provided": 1,
    "MYSM1-related_disorder|not_provided|Bone_marrow_failure_syndrome_4": 1,
    "Breast_neoplasm": 24,
    "Acromelic_frontonasal_dysostosis|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features": 4,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features": 12,
    "NFIA-related_disorder": 6,
    "Chromosome_1p32-p31_deletion_syndrome": 11,
    "Brain_malformations_with_or_without_urinary_tract_defects": 22,
    "NFIA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Brain_malformations_with_or_without_urinary_tract_defects|Chromosome_1p32-p31_deletion_syndrome": 1,
    "not_provided|Brain_malformations_with_or_without_urinary_tract_defects|Inborn_genetic_diseases": 1,
    "not_provided|NFIA-related_disorder|Brain_malformations_with_or_without_urinary_tract_defects": 1,
    "Chromosome_1p32-p31_deletion_syndrome|not_provided": 2,
    "Brain_malformations_with_or_without_urinary_tract_defects|not_provided|NFIA-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Brain_malformations_with_or_without_urinary_tract_defects": 1,
    "Brain_malformations_with_or_without_urinary_tract_defects|Inborn_genetic_diseases|not_provided": 1,
    "NFIA-related_disorder|not_provided": 5,
    "not_provided|NFIA-related_disorder": 7,
    "Brain_malformations_with_or_without_urinary_tract_defects|not_provided": 1,
    "Macrocephaly|Cleft_palate": 1,
    "NFIA-related_disorder|not_provided|Brain_malformations_with_or_without_urinary_tract_defects": 1,
    "not_provided|Chromosome_1p32-p31_deletion_syndrome": 1,
    "Brain_malformations_with_or_without_urinary_tract_defects|Chromosome_1p32-p31_deletion_syndrome": 1,
    "not_specified|NFIA-related_disorder": 1,
    "Inborn_genetic_diseases|Brain_malformations_with_or_without_urinary_tract_defects": 1,
    "NFIA-related_disorder|not_specified|not_provided": 1,
    "KANK4-related_disorder|not_provided": 9,
    "KANK4-related_disorder|not_provided|not_specified": 2,
    "KANK4-related_disorder": 13,
    "Nephrotic_syndrome": 69,
    "not_specified|KANK4-related_disorder": 3,
    "KANK4-related_disorder|not_provided|Nephrotic_syndrome": 1,
    "not_specified|not_provided|KANK4-related_disorder": 1,
    "not_provided|KANK4-related_disorder": 2,
    "KANK4-related_disorder|not_specified|not_provided": 1,
    "not_specified|KANK4-related_disorder|not_provided": 2,
    "not_provided|not_specified|KANK4-related_disorder": 3,
    "KANK4-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_23": 1241,
    "Developmental_and_epileptic_encephalopathy|_23|not_provided": 50,
    "not_provided|Developmental_and_epileptic_encephalopathy|_23|Inborn_genetic_diseases": 4,
    "Developmental_and_epileptic_encephalopathy|_23|Inborn_genetic_diseases": 39,
    "Developmental_and_epileptic_encephalopathy|_23|DOCK7-related_disorder": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_23|DOCK7-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_23|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_23": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_23": 48,
    "Developmental_and_epileptic_encephalopathy|_23|not_specified": 8,
    "DOCK7-related_disorder": 7,
    "not_provided|DOCK7-related_disorder|Developmental_and_epileptic_encephalopathy|_23": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_23": 42,
    "DOCK7-related_disorder|Developmental_and_epileptic_encephalopathy|_23": 6,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_23": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_23|not_provided": 6,
    "DOCK7-related_disorder|Developmental_and_epileptic_encephalopathy|_23|not_specified|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_23|not_specified|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_23|not_provided|DOCK7-related_disorder": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_23|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_23|not_provided|Inborn_genetic_diseases": 4,
    "not_specified|Developmental_and_epileptic_encephalopathy|_23": 3,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_23": 8,
    "DOCK7-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_23": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_23|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_23|not_provided|Inborn_genetic_diseases": 2,
    "Familial_hypobetalipoproteinemia_2": 5,
    "ANGPTL3-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_23|Familial_hypobetalipoproteinemia_2": 1,
    "not_provided|ANGPTL3-related_disorder|Familial_hypobetalipoproteinemia_2|Developmental_and_epileptic_encephalopathy|_23": 1,
    "Familial_hypobetalipoproteinemia_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Familial_hypobetalipoproteinemia_2": 1,
    "Developmental_and_epileptic_encephalopathy|_23|not_provided|Familial_hypobetalipoproteinemia_2": 1,
    "not_provided|ANGPTL3-related_disorder": 1,
    "Fetal_akinesia_deformation_sequence_3": 32,
    "not_specified|DOCK7-related_disorder|Developmental_and_epileptic_encephalopathy|_23|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_23": 1,
    "DOCK7-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_23": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_23|not_specified": 1,
    "not_specified|DOCK7-related_disorder": 1,
    "Autoimmune_disease|_susceptibility_to|_1": 1,
    "FOXD3-related_disorder": 7,
    "not_specified|ALG6-congenital_disorder_of_glycosylation_1C": 12,
    "ALG6-congenital_disorder_of_glycosylation_1C": 692,
    "not_specified|ALG6-congenital_disorder_of_glycosylation_1C|ALG6-related_disorder": 1,
    "not_provided|ALG6-congenital_disorder_of_glycosylation_1C": 16,
    "ALG6-congenital_disorder_of_glycosylation_1C|not_provided": 9,
    "Inborn_genetic_diseases|ALG6-congenital_disorder_of_glycosylation_1C": 5,
    "not_provided|ALG6-congenital_disorder_of_glycosylation_1C|not_specified": 2,
    "ALG6-related_disorder|ALG6-congenital_disorder_of_glycosylation_1C": 2,
    "ALG6-congenital_disorder_of_glycosylation_1C|ALG6-related_disorder": 3,
    "ALG6-related_disorder|Inborn_genetic_diseases|not_provided|ALG6-congenital_disorder_of_glycosylation_1C": 1,
    "not_provided|ALG6-congenital_disorder_of_glycosylation_1C|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_specified|ALG6-congenital_disorder_of_glycosylation_1C": 1,
    "ALG6-congenital_disorder_of_glycosylation_1C|not_specified": 8,
    "ALG6-related_disorder|not_specified|not_provided|ALG6-congenital_disorder_of_glycosylation_1C": 2,
    "ALG6-congenital_disorder_of_glycosylation_1C|Renal_cyst": 1,
    "not_specified|ALG6-congenital_disorder_of_glycosylation_1C|not_provided": 2,
    "ALG6-congenital_disorder_of_glycosylation_1C|Inborn_genetic_diseases": 2,
    "ALG6-congenital_disorder_of_glycosylation_1C|not_specified|not_provided": 2,
    "not_specified|not_provided|ALG6-congenital_disorder_of_glycosylation_1C": 2,
    "not_specified|Inborn_genetic_diseases|ALG6-congenital_disorder_of_glycosylation_1C": 1,
    "not_specified|ALG6-congenital_disorder_of_glycosylation_1C|ALG6-related_disorder|not_provided": 2,
    "ALG6-related_disorder|not_provided|ALG6-congenital_disorder_of_glycosylation_1C": 1,
    "not_provided|Inborn_genetic_diseases|ALG6-congenital_disorder_of_glycosylation_1C|not_specified": 1,
    "Postaxial_polydactyly": 2,
    "PGM1-congenital_disorder_of_glycosylation": 231,
    "not_provided|PGM1-congenital_disorder_of_glycosylation": 15,
    "PGM1-related_disorder|Inborn_genetic_diseases|PGM1-congenital_disorder_of_glycosylation": 1,
    "not_specified|PGM1-congenital_disorder_of_glycosylation": 6,
    "PGM1-congenital_disorder_of_glycosylation|PGM1-related_disorder|not_provided": 1,
    "PGM1-congenital_disorder_of_glycosylation|not_provided": 10,
    "PGM1-related_disorder": 8,
    "PGM1-related_disorder|PGM1-congenital_disorder_of_glycosylation": 5,
    "PGM1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 6,
    "not_provided|PGM1-congenital_disorder_of_glycosylation|not_specified": 2,
    "not_provided|not_specified|PGM1-congenital_disorder_of_glycosylation": 1,
    "Congenital_disorder_of_glycosylation|not_provided|PGM1-congenital_disorder_of_glycosylation|not_specified": 2,
    "PGM1-related_disorder|not_provided|PGM1-congenital_disorder_of_glycosylation": 3,
    "Inborn_genetic_diseases|not_specified|PGM1-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|PGM1-congenital_disorder_of_glycosylation": 8,
    "Congenital_disorder_of_glycosylation|not_specified|PGM1-congenital_disorder_of_glycosylation": 3,
    "not_provided|Inborn_genetic_diseases|PGM1-congenital_disorder_of_glycosylation": 2,
    "PGM1-related_disorder|Inborn_genetic_diseases|PGM1-congenital_disorder_of_glycosylation|not_provided": 1,
    "PGM1-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "Congenital_disorder_of_glycosylation|not_specified|not_provided|PGM1-congenital_disorder_of_glycosylation": 2,
    "PGM1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 5,
    "Congenital_disorder_of_glycosylation|PGM1-congenital_disorder_of_glycosylation": 6,
    "not_provided|Inborn_genetic_diseases|not_specified|PGM1-congenital_disorder_of_glycosylation": 1,
    "PGM1-related_disorder|PGM1-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "PGM1-congenital_disorder_of_glycosylation|PGM1-related_disorder|not_specified": 1,
    "not_specified|Congenital_disorder_of_glycosylation|not_provided|PGM1-congenital_disorder_of_glycosylation": 1,
    "PGM1-related_disorder|not_specified|PGM1-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|not_provided|PGM1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "Congenital_disorder_of_glycosylation|PGM1-congenital_disorder_of_glycosylation|PGM1-related_disorder|not_provided": 1,
    "PGM1-related_disorder|PGM1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_specified": 1,
    "PGM1-congenital_disorder_of_glycosylation|not_specified": 1,
    "PGM1-related_disorder|Congenital_disorder_of_glycosylation|PGM1-congenital_disorder_of_glycosylation": 2,
    "PGM1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PGM1-congenital_disorder_of_glycosylation|not_provided": 1,
    "Congenital_disorder_of_glycosylation|not_specified|PGM1-congenital_disorder_of_glycosylation|not_provided": 7,
    "PGM1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_provided": 1,
    "not_specified|PGM1-related_disorder": 1,
    "not_specified|not_provided|PGM1-congenital_disorder_of_glycosylation": 2,
    "Congenital_disorder_of_glycosylation|PGM1-congenital_disorder_of_glycosylation|not_provided": 3,
    "not_provided|Hearing_loss|_autosomal_recessive_108": 2,
    "ROR1-related_disorder": 2,
    "not_provided|ROR1-related_disorder": 8,
    "Hearing_loss|_autosomal_recessive_108|not_provided": 2,
    "not_specified|Hearing_loss|_autosomal_recessive_108|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_108|not_provided|not_specified": 1,
    "ROR1-related_disorder|not_provided": 3,
    "Hearing_loss|_autosomal_recessive_108": 2,
    "JAK1-related_disorder": 6,
    "JAK1-related_disorder|not_provided": 10,
    "Autoinflammation|_immune_dysregulation|_and_eosinophilia|not_provided": 4,
    "not_provided|JAK1-related_disorder": 9,
    "Autoinflammation|_immune_dysregulation|_and_eosinophilia": 9,
    "not_provided|not_specified|JAK1-related_disorder": 4,
    "not_provided|Autoinflammation|_immune_dysregulation|_and_eosinophilia": 2,
    "Acute_megakaryoblastic_leukemia_in_down_syndrome": 10,
    "not_specified|JAK1-related_disorder|not_provided": 1,
    "Autoinflammation|_immune_dysregulation|_and_eosinophilia|not_specified|not_provided": 2,
    "Autoinflammation|_immune_dysregulation|_and_eosinophilia|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_jak1_deficiency|Autoinflammation|_immune_dysregulation|_and_eosinophilia": 1,
    "not_provided|Autoinflammation|_immune_dysregulation|_and_eosinophilia|not_specified": 1,
    "Autoinflammation|_immune_dysregulation|_and_eosinophilia|Inborn_genetic_diseases|not_provided": 1,
    "Juvenile_onset_Parkinson_disease_19A": 146,
    "Juvenile_onset_Parkinson_disease_19A|not_provided": 8,
    "not_provided|Juvenile_onset_Parkinson_disease_19A": 10,
    "not_specified|Juvenile_onset_Parkinson_disease_19A": 1,
    "not_provided|Juvenile_onset_Parkinson_disease_19A|Inborn_genetic_diseases": 3,
    "Juvenile_onset_Parkinson_disease_19A|Prostate_cancer": 1,
    "Juvenile_onset_Parkinson_disease_19A|DNAJC6-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Juvenile_onset_Parkinson_disease_19A": 8,
    "not_specified|not_provided|Juvenile_onset_Parkinson_disease_19A": 6,
    "not_provided|not_specified|Juvenile_onset_Parkinson_disease_19A": 1,
    "DNAJC6-related_disorder|Juvenile_onset_Parkinson_disease_19A": 3,
    "Juvenile_onset_Parkinson_disease_19A|Juvenile-onset_diabetes_mellitus-central_and_peripheral_neurodegeneration_syndrome": 1,
    "Juvenile_onset_Parkinson_disease_19A|Inborn_genetic_diseases": 10,
    "Juvenile_onset_Parkinson_disease_19A|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Juvenile_onset_Parkinson_disease_19A": 1,
    "Juvenile_onset_Parkinson_disease_19A|not_provided|DNAJC6-related_disorder": 1,
    "not_provided|Juvenile_onset_Parkinson_disease_19A|DNAJC6-related_disorder": 1,
    "DNAJC6-related_disorder|not_provided|Juvenile_onset_Parkinson_disease_19A": 1,
    "Juvenile_onset_Parkinson_disease_19A|DNAJC6-related_disorder": 1,
    "Parkinson_disease_19B|_early-onset|Juvenile_onset_Parkinson_disease_19A": 1,
    "DNAJC6-related_disorder|Inborn_genetic_diseases|Juvenile_onset_Parkinson_disease_19A": 1,
    "Juvenile_onset_Parkinson_disease_19A|Parkinson_disease_19B|_early-onset": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency": 29,
    "Obesity_due_to_leptin_receptor_gene_deficiency|Monogenic_Non-Syndromic_Obesity": 6,
    "Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency": 3,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_leptin_receptor_gene_deficiency": 6,
    "Obesity_due_to_leptin_receptor_gene_deficiency|Monogenic_Non-Syndromic_Obesity|not_provided": 1,
    "LEPR-related_disorder": 181,
    "not_specified|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder": 1,
    "LEPR-related_disorder|not_provided": 12,
    "not_provided|Obesity_due_to_leptin_receptor_gene_deficiency": 5,
    "LEPR-related_disorder|Obesity_due_to_leptin_receptor_gene_deficiency": 7,
    "LEPR-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "LEPR-related_disorder|Inborn_genetic_diseases": 7,
    "Obesity_due_to_leptin_receptor_gene_deficiency|not_provided|Monogenic_Non-Syndromic_Obesity|not_specified|LEPTIN_RECEPTOR_POLYMORPHISM": 1,
    "not_specified|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency": 1,
    "not_provided|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder|Monogenic_diabetes": 1,
    "Monogenic_diabetes|LEPR-related_disorder": 2,
    "not_provided|LEPR-related_disorder": 6,
    "Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder|Inborn_genetic_diseases": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|not_provided|LEPR-related_disorder": 1,
    "not_provided|not_specified|Obesity_due_to_leptin_receptor_gene_deficiency": 1,
    "not_provided|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder": 1,
    "LEPR-related_disorder|Monogenic_diabetes|not_provided": 1,
    "Inborn_genetic_diseases|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder|Monogenic_Non-Syndromic_Obesity": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|Monogenic_Non-Syndromic_Obesity|not_provided|not_specified|LEPTIN_RECEPTOR_POLYMORPHISM": 2,
    "LEPR-related_disorder|Inborn_genetic_diseases|Obesity_due_to_leptin_receptor_gene_deficiency": 1,
    "Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder": 2,
    "not_provided|LEPR-related_disorder|Obesity_due_to_leptin_receptor_gene_deficiency": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|Monogenic_Non-Syndromic_Obesity|not_provided|not_specified": 1,
    "LEPR-related_disorder|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency": 3,
    "LEPR-related_disorder|not_specified": 1,
    "Monogenic_diabetes": 468,
    "not_provided|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder": 1,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_leptin_receptor_gene_deficiency|Inborn_genetic_diseases|LEPR-related_disorder": 1,
    "Inborn_genetic_diseases|LEPR-related_disorder": 7,
    "LEPR-related_disorder|Obesity_due_to_leptin_receptor_gene_deficiency|not_provided": 1,
    "Obesity_due_to_congenital_leptin_deficiency": 29,
    "not_specified|Inborn_genetic_diseases|LEPR-related_disorder": 1,
    "Monogenic_diabetes|not_provided|not_specified|Obesity_due_to_leptin_receptor_gene_deficiency": 1,
    "Inborn_genetic_diseases|LEPR-related_disorder|Obesity_due_to_leptin_receptor_gene_deficiency|not_provided": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|not_provided": 1,
    "not_specified|LEPR-related_disorder": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|Monogenic_Non-Syndromic_Obesity|not_provided|Monogenic_diabetes": 1,
    "Peripheral_precocious_puberty": 6,
    "Monogenic_diabetes|LEPR-related_disorder|Obesity_due_to_leptin_receptor_gene_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|not_specified|not_provided": 1,
    "not_specified|Monogenic_diabetes|Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|not_provided|not_specified": 1,
    "Monogenic_Non-Syndromic_Obesity|not_specified|Obesity_due_to_leptin_receptor_gene_deficiency|not_provided": 1,
    "Obesity_due_to_leptin_receptor_gene_deficiency|not_provided|Monogenic_Non-Syndromic_Obesity": 1,
    "not_provided|Inborn_genetic_diseases|LEPR-related_disorder": 1,
    "not_provided|LEPR-related_disorder|Monogenic_diabetes": 1,
    "Monogenic_Non-Syndromic_Obesity|LEPR-related_disorder|not_specified|not_provided|Obesity_due_to_leptin_receptor_gene_deficiency|Obesity": 1,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_leptin_receptor_gene_deficiency|LEPR-related_disorder|not_specified|not_provided|Monogenic_diabetes": 1,
    "not_specified|not_provided|LEPR-related_disorder": 1,
    "Schneckenbecken_dysplasia": 107,
    "Schneckenbecken_dysplasia|Inborn_genetic_diseases": 4,
    "Schneckenbecken_dysplasia|SLC35D1-related_disorder": 2,
    "Schneckenbecken_dysplasia|Connective_tissue_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Schneckenbecken_dysplasia": 1,
    "Sarcotubular_myopathy": 9,
    "Inborn_genetic_diseases|Schneckenbecken_dysplasia": 4,
    "not_specified|not_provided|Connective_tissue_disorder|Inborn_genetic_diseases|Schneckenbecken_dysplasia": 1,
    "Schneckenbecken_dysplasia|not_provided": 6,
    "SLC35D1-related_disorder|Schneckenbecken_dysplasia": 1,
    "not_provided|Schneckenbecken_dysplasia": 3,
    "Schneckenbecken_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "SLC35D1-related_disorder": 1,
    "not_provided|Schneckenbecken_dysplasia|Inborn_genetic_diseases": 1,
    "not_provided|Connective_tissue_disorder|Schneckenbecken_dysplasia|not_specified": 1,
    "Schneckenbecken_dysplasia|Connective_tissue_disorder|not_provided": 1,
    "Schneckenbecken_dysplasia|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "IL23R-related_disorder|not_provided": 4,
    "not_provided|IL23R-related_disorder": 1,
    "Inflammatory_bowel_disease_17|Psoriasis_7|_susceptibility_to|not_provided": 1,
    "not_provided|Psoriasis_7|_susceptibility_to|Inflammatory_bowel_disease_17": 1,
    "IL23R-related_disorder": 6,
    "not_provided|Inflammatory_bowel_disease_17|_protection_against|Psoriasis|_protection_against": 1,
    "IL12RB2-related_disorder|not_provided": 15,
    "not_provided|IL12RB2-related_disorder": 9,
    "IL12RB2-related_disorder": 1,
    "not_specified|IL12RB2-related_disorder|not_provided": 1,
    "DIRAS3-related_disorder": 1,
    "not_provided|WLS-related_disorder": 1,
    "WLS_syndrome|Zaki_syndrome": 4,
    "not_specified|Zaki_syndrome": 2,
    "WLS-related_disorder": 3,
    "Zaki_syndrome": 6,
    "Zaki_syndrome|not_specified": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa": 7,
    "Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_2": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2": 13,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis": 1,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_2": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|not_provided": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2": 6,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|not_specified|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 263,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided": 7,
    "Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20": 5,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 276,
    "RPE65-related_recessive_retinopathy": 19,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy": 6,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|Leber_congenital_amaurosis": 5,
    "Leber_congenital_amaurosis_2": 34,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|RPE65-related_recessive_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|RPE65-related_disorder|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 4,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 7,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Leber_congenital_amaurosis": 21,
    "Leber_congenital_amaurosis|Retinal_dystrophy": 6,
    "Leber_congenital_amaurosis|not_specified": 7,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Leber_congenital_amaurosis": 4,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 3,
    "RPE65-related_disorder|Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_specified|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|not_provided": 4,
    "not_specified|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa_20": 11,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis": 7,
    "not_provided|Retinitis_pigmentosa_20|Retinal_dystrophy|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_disorder|Neurodevelopmental_disorder|Leber_congenital_amaurosis_2": 1,
    "RPE65-related_recessive_retinopathy|not_provided|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement": 3,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 2,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 2,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided": 35,
    "not_specified|not_provided|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2": 1,
    "Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa": 3,
    "Retinal_dystrophy|Abnormality_of_vision|Abnormal_electroretinogram|Congenital_blindness|Retinal_degeneration|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy": 1,
    "Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 2,
    "Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy": 1,
    "not_provided|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 4,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_specified": 1,
    "RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|RPE65-related_recessive_retinopathy|not_specified": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis": 3,
    "Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 4,
    "Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 2,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis|RPE65-related_disorder|not_provided": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 3,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_15|Leber_congenital_amaurosis_2|Retinal_dystrophy|Retinitis_pigmentosa_20": 1,
    "RPE65-related_recessive_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 1,
    "Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy": 4,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 2,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa|RPE65-related_recessive_retinopathy": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|not_specified": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|not_specified|Retinitis_pigmentosa|RPE65-related_recessive_retinopathy|not_provided": 1,
    "Leber_congenital_amaurosis_2|Retinal_dystrophy|RPE65-related_disorder|Retinitis_pigmentosa_20|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy": 1,
    "Autosomal_recessive_retinitis_pigmentosa|RPE65-related_recessive_retinopathy": 3,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|RPE65-related_disorder|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_specified|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa": 1,
    "RPE65-related_recessive_retinopathy|not_provided": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|RPE65-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_2|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20": 2,
    "not_specified|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 7,
    "RPE65-related_recessive_retinopathy|Autism|Global_developmental_delay|Retinal_dystrophy|Rod-cone_dystrophy|Nystagmus": 1,
    "RPE65-related_recessive_retinopathy|not_provided|RPE65-related_disorder|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|not_specified|not_provided|Retinal_dystrophy|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis|not_provided|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Autosomal_recessive_retinitis_pigmentosa": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis": 3,
    "RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 1,
    "RPE65-related_recessive_retinopathy|not_specified|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Retinitis_pigmentosa": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis|Retinitis_pigmentosa|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 1,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 2,
    "not_provided|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_specified|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Joubert_syndrome_9": 1,
    "not_provided|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 3,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "Abnormality_of_the_eye": 13,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 2,
    "not_provided|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis|Retinitis_pigmentosa_20": 1,
    "not_provided|Leber_congenital_amaurosis_2": 3,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|not_specified|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_specified": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Inborn_genetic_diseases": 3,
    "Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2": 1,
    "not_provided|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2": 2,
    "Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Congenital_isolated_adrenocorticotropic_hormone_deficiency|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 2,
    "not_provided|RPE65-related_recessive_retinopathy": 2,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinal_dystrophy|Retinitis_pigmentosa_20": 1,
    "RPE65-related_recessive_retinopathy|not_provided|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_specified": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "not_specified|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Retinal_dystrophy|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 1,
    "Congenital_isolated_adrenocorticotropic_hormone_deficiency": 65,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|not_specified|Retinitis_pigmentosa_20": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinal_dystrophy|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_2": 1,
    "RPE65-related_disorder": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "not_specified|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|RPE65-related_recessive_retinopathy|RPE65-related_disorder": 1,
    "Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_specified|not_provided": 1,
    "not_provided|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "RPE65-related_disorder|not_provided|Retinitis_pigmentosa|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Leber_congenital_amaurosis": 1,
    "RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 3,
    "not_provided|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided|RPE65-related_disorder|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy": 1,
    "Cone-rod_dystrophy_15|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "RPE65-related_recessive_retinopathy|not_provided|Leber_congenital_amaurosis_2": 2,
    "RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinal_dystrophy|Retinitis_pigmentosa_20|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy|RPE65-related_recessive_retinopathy": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|RPE65-related_recessive_retinopathy": 3,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "RPE65-related_disorder|RPE65-related_recessive_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided|Inborn_genetic_diseases|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinal_dystrophy": 1,
    "not_specified|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy": 1,
    "RPE65-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa|RPE65-related_recessive_retinopathy": 1,
    "not_provided|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy": 1,
    "RPE65-related_disorder|RPE65-related_recessive_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|Retinal_dystrophy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis": 1,
    "RPE65-related_disorder|Leber_congenital_amaurosis|Retinitis_pigmentosa|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Inborn_genetic_diseases|Retinitis_pigmentosa|Retinal_dystrophy|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided": 1,
    "RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_disorder|Leber_congenital_amaurosis|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Abnormality_of_the_eye": 1,
    "Leber_congenital_amaurosis|not_provided|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinal_dystrophy|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinal_dystrophy|Retinitis_pigmentosa_87_with_choroidal_involvement": 1,
    "Leber_congenital_amaurosis_2|Retinal_dystrophy": 1,
    "not_provided|RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Leber_congenital_amaurosis": 1,
    "RPE65-related_disorder|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2": 1,
    "Leber_congenital_amaurosis_2|RPE65-related_recessive_retinopathy|not_provided": 1,
    "RPE65-related_recessive_retinopathy|RPE65-related_disorder|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis|Autosomal_recessive_retinitis_pigmentosa": 1,
    "RPE65-related_recessive_retinopathy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|RPE65-related_disorder|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|not_provided|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|RPE65-related_recessive_retinopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "RPE65-related_recessive_retinopathy|not_provided|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|RPE65-related_recessive_retinopathy|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Leber_congenital_amaurosis_2|Retinitis_pigmentosa|Retinitis_pigmentosa_20": 1,
    "RPE65-related_recessive_retinopathy|not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|not_provided|RPE65-related_recessive_retinopathy": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy|Retinitis_pigmentosa_20|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Leber_congenital_amaurosis|RPE65-related_recessive_retinopathy|not_specified|not_provided": 1,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20": 1,
    "Leber_congenital_amaurosis_2|Retinitis_pigmentosa_87_with_choroidal_involvement|Retinitis_pigmentosa_20|RPE65-related_disorder|RPE65-related_recessive_retinopathy|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis_2|Retinitis_pigmentosa_20|Retinitis_pigmentosa_87_with_choroidal_involvement|Leber_congenital_amaurosis": 1,
    "LRRC7-associated_disorder": 1,
    "LRRC7-associated_neurodevelopmental_disorder": 1,
    "LRRC7-associated_obesity_and_neurodevelopmental_disorder": 2,
    "SRSF11-related_disorder": 2,
    "Cystathioninuria": 39,
    "not_provided|Cystathioninuria": 7,
    "Cystathioninuria|Inborn_genetic_diseases": 1,
    "Cystathioninuria|not_provided": 5,
    "CTH-related_disorder": 1,
    "CTH-related_disorder|not_provided|Cystathioninuria": 3,
    "Inborn_genetic_diseases|Cystathioninuria": 2,
    "CTH-related_disorder|not_provided|Cystathioninuria|Homocysteine_level_elevated": 1,
    "not_provided|NEGR1-related_disorder": 1,
    "LRRIQ3-related_disorder": 9,
    "LRRIQ3-related_disorder|not_provided": 1,
    "Atrial_conduction_disease": 8,
    "Inborn_genetic_diseases|Atrial_conduction_disease|not_provided": 7,
    "Meniere_disease|not_provided": 14,
    "not_provided|Atrial_conduction_disease": 11,
    "Inborn_genetic_diseases|not_provided|Atrial_conduction_disease": 3,
    "not_specified|not_provided|TNNI3K-related_disorder": 3,
    "Atrial_conduction_disease|not_specified|not_provided": 3,
    "Atrial_conduction_disease|not_provided": 19,
    "TNNI3K-related_disorder|not_provided": 3,
    "not_provided|TNNI3K-related_disorder": 8,
    "FPGT-TNNI3K-related_disorder|not_provided": 1,
    "not_specified|Atrial_conduction_disease|TNNI3K-related_disorder|not_provided": 1,
    "Atrial_conduction_disease|not_provided|TNNI3K-related_disorder": 1,
    "Atrial_conduction_disease|TNNI3K-related_disorder|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided|Atrial_conduction_disease": 1,
    "not_provided|Atrial_conduction_disease|Primary_dilated_cardiomyopathy": 1,
    "not_specified|TNNI3K-related_disorder|not_provided": 1,
    "TNNI3K-related_disorder|Atrial_conduction_disease|not_specified|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Atrial_conduction_disease": 3,
    "TNNI3K-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Atrial_conduction_disease|Meniere_disease|not_provided|Inborn_genetic_diseases": 1,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Meniere_disease": 10,
    "Arrhythmogenic_right_ventricular_dysplasia_2": 6,
    "Atrial_conduction_disease|not_provided|Inborn_genetic_diseases": 1,
    "Atrial_conduction_disease|not_provided|not_specified": 1,
    "Atrial_conduction_disease|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|TNNI3K-related_disorder|Atrial_conduction_disease": 1,
    "TNNI3K-related_disorder|not_specified|not_provided": 1,
    "not_provided|Atrial_conduction_disease|TNNI3K-related_disorder|not_specified": 1,
    "TNNI3K-related_disorder|not_provided|not_specified": 2,
    "not_provided|Atrial_conduction_disease|See_cases": 1,
    "Atrial_conduction_disease|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Atrial_conduction_disease|Inborn_genetic_diseases": 1,
    "FPGT-TNNI3K-related_disorder|not_specified|not_provided": 1,
    "not_provided|TNNI3K-related_disorder|not_specified": 1,
    "FPGT-TNNI3K-related_disorder": 1,
    "CRYZ-related_disorder": 5,
    "not_provided|CRYZ-related_disorder": 1,
    "CRYZ-related_disorder|not_provided": 1,
    "not_specified|CRYZ-related_disorder": 1,
    "not_provided|LHX8-related_disorder": 3,
    "LHX8-related_disorder": 5,
    "LHX8-related_disorder|not_provided": 2,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 705,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided": 44,
    "not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 49,
    "not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_specified": 1,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|ACADM-related_disorder": 3,
    "Inborn_genetic_diseases|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 5,
    "not_specified|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 17,
    "not_provided|not_specified|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 4,
    "ACADM-related_disorder|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 5,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_specified": 8,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|Inborn_genetic_diseases": 13,
    "ACADM-related_disorder|not_specified|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|See_cases": 1,
    "ACADM-related_disorder|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 3,
    "Inborn_genetic_diseases|not_specified|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "not_specified|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 7,
    "not_specified|not_provided|.|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|See_cases": 1,
    "not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|ACADM-related_disorder": 1,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided|not_specified": 2,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided|ACADM-related_disorder": 2,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|Inborn_genetic_diseases|See_cases": 1,
    "ACADM-related_disorder|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_specified": 1,
    "ACADM-related_disorder|not_specified|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "ACADM-related_disorder|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 2,
    "not_specified|ACADM-related_disorder|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided": 1,
    "not_provided|ACADM-related_disorder|Inborn_genetic_diseases|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "ACADM-related_disorder|not_specified|Inborn_genetic_diseases|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided": 1,
    "not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|ACADM-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|ACADM-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "ACADM-related_disorder": 2,
    "Epileptic_spasm|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|ACADM-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided": 1,
    "ACADM-related_disorder|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|Deficiency_of_butyryl-CoA_dehydrogenase": 1,
    "Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|See_cases": 1,
    "ACADM-related_disorder|Inborn_genetic_diseases|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|Epileptic_spasm|See_cases": 1,
    "not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|ACADM-related_disorder|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "MCADD_-_Medium-chain_acyl-CoA_dehydrogenase_deficiency_\u2013_full_ACADM_sequencing_newborn_screening_follow_up|ACADM-related_disorder|Inborn_genetic_diseases|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "not_specified|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency|not_provided": 2,
    "not_specified|See_cases|not_provided|Medium-chain_acyl-coenzyme_A_dehydrogenase_deficiency": 1,
    "Premature_ovarian_failure_20|Spermatogenic_failure_2": 5,
    "Spermatogenic_failure_2": 4,
    "Genetic_non-acquired_premature_ovarian_failure": 50,
    "Non-obstructive_azoospermia": 49,
    "Spermatogenic_failure_2|Premature_ovarian_failure_20|Non-obstructive_azoospermia": 1,
    "Genetic_non-acquired_premature_ovarian_failure|Spermatogenic_failure_2": 1,
    "Spermatogenic_failure_2|Premature_ovarian_failure_20|Oligospermia|Non-obstructive_azoospermia|Premature_ovarian_insufficiency": 1,
    "Premature_ovarian_failure_20": 1,
    "MSH4-related_condition": 1,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia_and_cerebellar_atrophy|_with_or_without_seizures": 3,
    "Neurodevelopmental_disorder_with_hypotonia_and_cerebellar_atrophy|_with_or_without_seizures": 8,
    "Neurodevelopmental_disorder_with_hypotonia_and_cerebellar_atrophy|_with_or_without_seizures|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_cerebellar_atrophy|_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Dilated_Cardiomyopathy|_Dominant": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 25,
    "Cardiovascular_phenotype|NEXN-related_disorder": 2,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 98,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 69,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided": 3,
    "Cardiomyopathy": 3601,
    "Cardiomyopathy|Cardiovascular_phenotype": 149,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided": 6,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided": 4,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 2,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 2,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 18,
    "not_specified|Cardiovascular_phenotype|not_provided": 66,
    "not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 26,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype": 14,
    "Dilated_cardiomyopathy_1CC|not_provided": 2,
    "NEXN-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy": 105,
    "not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 5,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 3,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Left_ventricular_hypertrophy": 1,
    "NEXN-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 2,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 2,
    "not_provided|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 4,
    "not_specified|Cardiomyopathy|not_provided": 11,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_20": 1,
    "not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 6,
    "Dilated_cardiomyopathy_1A": 45,
    "Cardiomyopathy|not_provided": 118,
    "not_provided|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1CC": 2,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified": 1,
    "not_provided|not_specified|NEXN-related_disorder|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "Cardiovascular_phenotype|NEXN-related_disorder|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "NEXN-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype|not_provided": 3,
    "Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_20": 1,
    "Hypertrophic_cardiomyopathy_2": 28,
    "NEXN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|NEXN-related_disorder|not_specified": 1,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 2,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided|Cardiovascular_phenotype": 4,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "Hypertrophic_cardiomyopathy_20|not_provided|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy|not_specified|Premature_ventricular_contraction|not_provided": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified": 2,
    "Cardiovascular_phenotype|NEXN-related_disorder|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1": 330,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "CARDIOMYOPATHY|_DILATED|_2M": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|CARDIOMYOPATHY|_DILATED|_2M|Hypertrophic_cardiomyopathy_20|not_provided|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided|Cardiomyopathy": 1,
    "NEXN-related_disorder|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 4,
    "not_provided|NEXN-related_disorder|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 1,
    "NEXN-related_disorder|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Heart_failure": 1,
    "not_provided|Cardiomyopathy": 108,
    "Cardiovascular_phenotype|Cardiomyopathy|NEXN-related_disorder|not_specified|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 8,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided": 1,
    "Cardiovascular_phenotype|NEXN-related_disorder|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Primary_familial_dilated_cardiomyopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "NEXN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "See_cases|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "Cardiovascular_phenotype|NEXN-related_disorder|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|NEXN-related_disorder": 1,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "NEXN-related_disorder|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|NEXN-related_disorder|not_provided|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|Long_QT_syndrome": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified|not_provided": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|NEXN-related_disorder|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|not_specified": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 2,
    "not_specified|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC": 1,
    "not_provided|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Cardiomyopathy|not_provided|NEXN-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_20|Dilated_cardiomyopathy_1CC|Dilated_cardiomyopathy_1S|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "NEXN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 14,
    "Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Dilated_cardiomyopathy_1CC|Hypertrophic_cardiomyopathy_20": 1,
    "DNAJB4-related_disorder": 3,
    "Congenital_myopathy_21_with_early_respiratory_failure": 4,
    "Multisystem_inflammatory_syndrome_in_children": 14,
    "Susceptibility_to_severe_COVID-19": 43,
    "ADGRL2-related_disorder": 24,
    "not_provided|ADGRL2-related_disorder": 2,
    "ADGRL2-related_disorder|not_provided": 2,
    "not_specified|ADGRL2-related_disorder": 1,
    "PRKACB-related_disorder": 3,
    "Cardioacrofacial_dysplasia_2": 9,
    "Immunodeficiency_37": 86,
    "Immunodeficiency_37|Mesothelioma|_malignant|Mucosa-associated_lymphoma|Lymphoma|_non-Hodgkin|_familial|Germ_cell_tumor_of_testis": 1,
    "not_provided|Immunodeficiency_37|not_specified": 1,
    "Follicular_lymphoma": 6,
    "Immunodeficiency_37|not_provided": 2,
    "Inborn_genetic_diseases|Immunodeficiency_37": 2,
    "Mesothelioma|Mucosa-associated_lymphoma|MALE_GERM_CELL_TUMOR|_SOMATIC": 1,
    "BCL10-related_disorder|Immunodeficiency_37": 3,
    "Malignant_tumor_of_testis": 1,
    "Sezary_syndrome": 1,
    "Mucosa-associated_lymphoma": 2,
    "Van_Maldergem_syndrome_2": 26,
    "Immunodeficiency_37|Inborn_genetic_diseases": 1,
    "BCL10-related_disorder": 1,
    "Immunodeficiency_37|not_specified": 1,
    "MALE_GERM_CELL_TUMOR|_SOMATIC|Immunodeficiency_37": 1,
    "MALE_GERM_CELL_TUMOR|_SOMATIC": 1,
    "T-cell_acute_lymphoblastic_leukemia|Carcinoma_of_colon": 1,
    "Mesothelioma": 2,
    "Immunodeficiency_37|not_provided|not_specified": 1,
    "not_provided|Immunodeficiency_37|BCL10-related_disorder": 1,
    "Autism|not_specified": 6,
    "Neurofacioskeletal_syndrome_with_or_without_renal_agenesis": 6,
    "Inborn_genetic_diseases|HS2ST1-related_disorder": 1,
    "NEUROFACIOSKELETAL_SYNDROME_WITHOUT_RENAL_AGENESIS": 2,
    "Neurofacioskeletal_syndrome_with_or_without_renal_agenesis|not_provided": 1,
    "Inherited_susceptibility_to_mycobacterial_diseases": 2,
    "Telangiectasia|_impaired_intellectual_development|_microcephaly|_metaphyseal_dysplasia|_eye_abnormalities|_and_short_stature": 2,
    "Myopia_21|_autosomal_dominant": 8,
    "ZNF644-related_disorder": 8,
    "not_specified|ZNF644-related_disorder": 2,
    "not_specified|Myopia_21|_autosomal_dominant": 2,
    "not_provided|ZNF644-related_disorder": 2,
    "Premature_ovarian_failure_9": 14,
    "Azoospermia": 15,
    "not_provided|Premature_ovarian_failure_9": 1,
    "HFM1-related_disorder": 8,
    "not_specified|not_provided|HFM1-related_disorder": 1,
    "Spermatogenic_failure_4": 18,
    "Prostate_cancer|Infertility_disorder|not_specified": 1,
    "TGFBR3-related_disorder": 14,
    "TGFBR3-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR3-related_disorder|not_provided": 2,
    "not_provided|TGFBR3-related_disorder": 2,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR3-related_disorder": 1,
    "not_provided|TGFBR3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "BRDT-related_disorder": 3,
    "Spermatogenic_failure_21": 1,
    "Intellectual_disability|_autosomal_dominant_58": 23,
    "Male_infertility": 81,
    "Glomuvenous_malformation": 47,
    "not_provided|Glomuvenous_malformation": 6,
    "Blue_rubber_bleb_nevus": 1,
    "Glomuvenous_malformation|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Glomuvenous_malformation": 5,
    "Glomuvenous_malformation|GLMN-related_disorder": 1,
    "not_provided|Vascular_skin_disorders|Glomuvenous_malformation": 1,
    "GLMN-related_disorder|not_specified|not_provided|Glomuvenous_malformation": 2,
    "GLMN-related_disorder|not_provided|Glomuvenous_malformation": 1,
    "Glomuvenous_malformation|not_provided": 4,
    "not_provided|GLMN-related_disorder|Glomuvenous_malformation": 1,
    "Glomuvenous_malformation|not_provided|GLMN-related_disorder": 1,
    "Glomuvenous_malformation|GLMN-related_disorder|not_provided": 2,
    "Glomuvenous_malformation|Blue_rubber_bleb_nevus": 1,
    "GLMN-related_disorder|Inborn_genetic_diseases|not_provided|Glomuvenous_malformation": 1,
    "Glomuvenous_malformation|Venous_malformation|not_provided": 1,
    "not_provided|Glomuvenous_malformation|not_specified": 1,
    "not_specified|Glomuvenous_malformation|not_provided": 1,
    "not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 74,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_specified": 58,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant": 146,
    "not_specified|not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 5,
    "not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_specified": 3,
    "not_specified|GFI1-related_disorder|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_specified|not_provided": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_provided|GFI1-related_disorder|not_specified": 1,
    "not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 1,
    "GFI1-related_disorder|not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 5,
    "not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant|GFI1-related_disorder": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_provided|not_specified": 2,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_specified|GFI1-related_disorder": 1,
    "not_specified|GFI1-related_disorder|not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "Severe_congenital_neutropenia|not_specified|not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 4,
    "Nonimmune_chronic_idiopathic_neutropenia_of_adults|Neutropenia|_severe_congenital|_2|_autosomal_dominant|GFI1-related_disorder|not_provided|not_specified": 1,
    "GFI1-related_disorder|not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Severe_congenital_neutropenia|not_provided": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|GFI1-related_disorder|not_specified": 1,
    "GFI1-related_disorder|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Severe_congenital_neutropenia": 1,
    "Severe_congenital_neutropenia|not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "Severe_congenital_neutropenia|not_specified|not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_provided": 4,
    "Severe_congenital_neutropenia|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults|not_specified|not_provided": 2,
    "not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_provided": 3,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_provided|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant|GFI1-related_disorder|not_specified": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_specified": 8,
    "GFI1-related_disorder|not_specified": 2,
    "not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_specified|not_provided|Nonimmune_chronic_idiopathic_neutropenia_of_adults": 1,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults|not_specified": 1,
    "not_specified|GFI1-related_disorder": 1,
    "not_provided|not_specified|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 2,
    "Neutropenia|_severe_congenital|_2|_autosomal_dominant|Nonimmune_chronic_idiopathic_neutropenia_of_adults|not_provided": 1,
    "GFI1-related_disorder|Neutropenia|_severe_congenital|_2|_autosomal_dominant|not_provided": 1,
    "GFI1-related_disorder|Neutropenia|_severe_congenital|_2|_autosomal_dominant": 1,
    "EVI5-related_disorder": 1,
    "Diamond-Blackfan_anemia_6": 52,
    "Diamond-Blackfan_anemia_6|not_provided": 2,
    "not_specified|Diamond-Blackfan_anemia_6": 1,
    "Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia": 14,
    "RPL5-related_disorder|not_specified|not_provided|Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia": 2,
    "Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia|not_specified": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_6": 29,
    "not_provided|Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia": 1,
    "RPL5-related_disorder": 4,
    "not_provided|Diamond-Blackfan_anemia": 11,
    "Hemangioma|Hypotelorism|Hepatomegaly|Atrial_septal_defect|Relative_macrocephaly|Lateral_ventricle_dilatation|Intracerebral_periventricular_calcifications|Abnormal_pinna_morphology|Erythroid_hypoplasia|Vaginal_hydrocele|Aplasia_of_the_ovary|Wide_anterior_fontanel|Low-set|_posteriorly_rotated_ears|Aplastic_anemia|Dry_skin|Downslanted_palpebral_fissures|Pulmonary_arterial_hypertension": 1,
    "not_provided|Diamond-Blackfan_anemia_6|not_specified|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_6|not_provided": 1,
    "not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_6|not_specified": 1,
    "RPL5-related_disorder|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_6|not_provided|not_specified|Diamond-Blackfan_anemia": 1,
    "not_specified|Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_6|RPL5-related_disorder|Diamond-Blackfan_anemia": 1,
    "not_specified|not_provided|Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia": 1,
    "not_specified|Diamond-Blackfan_anemia_6|not_provided|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_6|not_provided|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia|not_specified|RPL5-related_disorder|Diamond-Blackfan_anemia_6": 1,
    "Diamond-Blackfan_anemia|RPL5-related_disorder": 1,
    "Diamond-Blackfan_anemia|RPL5-related_disorder|Diamond-Blackfan_anemia_6": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_6|not_specified": 1,
    "not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_6": 1,
    "Diamond-Blackfan_anemia_6|Diamond-Blackfan_anemia|not_provided": 1,
    "Thalidomide_response": 15,
    "CCDC18-related_disorder": 26,
    "CCDC18-related_disorder|not_provided": 2,
    "CCDC18-related_disorder|not_specified": 1,
    "Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Macular_degeneration": 1,
    "Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 4,
    "ABCA4-related_disorder": 26,
    "Macular_degeneration|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 7,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Macular_degeneration": 1,
    "Macular_degeneration|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder": 2,
    "ABCA4-related_disorder|not_specified|not_provided": 2,
    "Cone-rod_dystrophy_3": 13,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinal_dystrophy": 4,
    "not_provided|Retinal_dystrophy|Stargardt_disease": 3,
    "Retinal_dystrophy|ABCA4-related_disorder|not_provided": 3,
    "ABCA4-related_disorder|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided": 1,
    "ABCA4-related_disorder|not_specified|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "not_specified|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Macular_degeneration": 1,
    "Severe_early-childhood-onset_retinal_dystrophy": 80,
    "ABCA4-related_disorder|not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_specified|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease": 4,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|Retinal_dystrophy": 7,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy": 20,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|not_provided": 4,
    "not_provided|ABCA4-related_disorder": 23,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 5,
    "ABCA4-related_disorder|not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone_dystrophy|Retinal_dystrophy": 1,
    "Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided": 5,
    "not_provided|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Stargardt_disease": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided": 4,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder|Stargardt_Disease|_Recessive|not_specified|not_provided|MACULAR_DEGENERATION|_AGE-RELATED|_2|_SUSCEPTIBILITY_TO|Macular_degeneration": 1,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 48,
    "not_specified|not_provided|ABCA4-related_disorder|Retinal_dystrophy": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided": 24,
    "Stargardt_disease|Retinal_dystrophy|not_provided": 3,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy": 42,
    "Age_related_macular_degeneration_2|Retinal_disorder|Visual_impairment|Retinal_dystrophy": 1,
    "Stargardt_disease|not_provided": 17,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder|Macular_degeneration|Blindness|Visual_loss": 1,
    "ABCA4-related_disorder|not_provided": 34,
    "ABCA4-related_disorder|Macular_degeneration|not_provided|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive": 3,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "not_provided|Stargardt_disease": 20,
    "Retinal_dystrophy|not_provided|Stargardt_disease|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 2,
    "Retinitis_pigmentosa_19": 10,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "not_provided|Retinal_disorders|Retinal_dystrophy": 2,
    "Age_related_macular_degeneration_2|not_provided|not_specified|Cone-rod_dystrophy": 1,
    "ABCA4-related_disorder|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinal_dystrophy|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Macular_degeneration|Stargardt_Disease|_Recessive|ABCA4-related_disorder|Cone-Rod_Dystrophy|_Recessive": 1,
    "Macular_dystrophy|ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Optic_atrophy|not_provided|Stargardt_disease": 1,
    "Stargardt_disease|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Retinitis_pigmentosa|not_provided": 1,
    "ABCA4-related_retinopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Age_related_macular_degeneration_2|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "not_specified|Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|not_provided|Macular_degeneration": 1,
    "ABCA4-related_disorder|not_specified|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Macular_degeneration": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|not_specified|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Age_related_macular_degeneration_2|Stargardt_disease": 1,
    "Congenital_stationary_night_blindness": 27,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|not_provided": 1,
    "not_specified|not_provided|Cone-rod_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_3|Stargardt_disease": 1,
    "Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided": 3,
    "Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|ABCA4-related_disorder|Retinal_dystrophy|not_specified|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease|Cone_dystrophy|Macular_degeneration": 1,
    "Retinitis_pigmentosa_19|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "not_specified|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "ABCA4-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "ABCA4-related_disorder|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19": 3,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 3,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 43,
    "ABCA4-related_disorder|Progressive_cone_dystrophy_(without_rod_involvement)|Macular_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Vitreoretinopathy": 1,
    "ABCA4-related_retinopathy|ABCA4-related_disorder|Retinal_disorders|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Leber_congenital_amaurosis_14|Retinal_dystrophy|_early-onset_severe|Stargardt_disease": 1,
    "Retinal_disorders|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Stargardt_disease": 1,
    "Stargardt_disease": 35,
    "ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19": 4,
    "not_provided|not_specified|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "Cone_dystrophy|not_provided|Retinal_dystrophy": 1,
    "Age_related_macular_degeneration_2": 6,
    "not_provided|ABCA4-related_retinopathy": 3,
    "not_provided|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive": 1,
    "Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_provided|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|maculopathy|See_cases": 1,
    "Retinal_dystrophy|Stargardt_disease": 3,
    "ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Vitreoretinopathy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Stargardt_disease": 1,
    "ABCA4-related_retinopathy|Macular_dystrophy|ABCA4-related_disorder|Syndromic_retinitis_pigmentosa|Retinal_disorders|Retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Inborn_genetic_diseases|Age_related_macular_degeneration_2|not_specified|not_provided|Retinitis_pigmentosa|Stargardt_disease|MACULAR_DEGENERATION|_AGE-RELATED|_2|_SUSCEPTIBILITY_TO|Cone_dystrophy|See_cases": 1,
    "ABCA4-related_disorder|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Macular_degeneration": 1,
    "ABCA4-related_disorder|not_specified|not_provided|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "not_specified|not_provided|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 3,
    "not_provided|maculopathy|Retinal_dystrophy": 1,
    "not_provided|Stargardt_disease|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "ABCA4-related_disorder|not_provided|Retinal_dystrophy|not_specified|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "not_provided|Stargardt_disease|Retinal_dystrophy": 3,
    "not_provided|Retinal_dystrophy|not_specified": 21,
    "not_specified|not_provided|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "Cone-rod_dystrophy|Stargardt_disease|ABCA4-related_disorder|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Optic_atrophy|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy": 53,
    "Macular_degeneration|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Cone-Rod_Dystrophy|_Recessive": 2,
    "ABCA4-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Stargardt_disease": 1,
    "Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "Retinal_dystrophy|not_specified|not_provided|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "not_provided|Age_related_macular_degeneration_2": 2,
    "not_provided|Retinitis_pigmentosa_19": 5,
    "Age_related_macular_degeneration_2|Retinal_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Retinal_dystrophy|not_provided": 3,
    "Autosomal_recessive_retinitis_pigmentosa": 44,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Retinitis_pigmentosa": 1,
    "ABCA4-related_retinopathy|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration": 1,
    "ABCA4-related_disorder|not_provided|Retinal_dystrophy": 2,
    "not_provided|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided": 1,
    "Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided": 1,
    "Cone-rod_dystrophy|Retinal_dystrophy|not_provided": 3,
    "not_provided|Cone-rod_dystrophy": 16,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3": 1,
    "ABCA4-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "Inborn_genetic_diseases|Macular_dystrophy|ABCA4-related_disorder|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Benign_concentric_annular_macular_dystrophy|Age_related_macular_degeneration_2|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "not_specified|not_provided|Stargardt_disease": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Stargardt_disease": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Macular_degeneration|not_provided|Stargardt_Disease|_Recessive|ABCA4-related_disorder|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 3,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|Retinitis_pigmentosa": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Stargardt_disease": 1,
    "Optic_atrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_specified|not_provided": 1,
    "Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_retinopathy|Isolated_macular_dystrophy": 1,
    "Stargardt_disease|Cone_dystrophy_and_rod_monochromatism": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|ABCA4-related_disorder|Stargardt_disease": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder": 1,
    "Cone-rod_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease|Retinal_dystrophy|Age_related_macular_degeneration_2|not_provided": 1,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3": 1,
    "not_provided|Isolated_macular_dystrophy": 3,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_specified|not_provided": 1,
    "Macular_dystrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Stargardt_disease|Cone-rod_dystrophy|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_specified": 1,
    "Retinal_dystrophy|not_provided|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy": 4,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|maculopathy": 1,
    "Retinal_dystrophy|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Retinitis_pigmentosa": 2,
    "not_provided|Age_related_macular_degeneration_2|Retinal_disorder|Visual_impairment|Retinal_dystrophy": 1,
    "Cone_dystrophy|ABCA4-related_disorder|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|not_provided": 1,
    "ABCA4-related_retinopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|ABCA4-related_disorder|not_provided": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Cone-rod_dystrophy|Retinitis_pigmentosa_1|Retinitis_pigmentosa_19": 1,
    "Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinal_dystrophy|not_provided": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "not_provided|Optic_atrophy": 25,
    "Retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease|Cone-rod_dystrophy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|not_provided": 1,
    "ABCA4-related_retinopathy": 4,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 39,
    "Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19": 1,
    "Cone-rod_dystrophy_3|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "ABCA4-related_disorder|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Macular_dystrophy|not_provided": 4,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "ABCA4-related_disorder|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Stargardt_disease": 1,
    "Age_related_macular_degeneration_2|Retinal_dystrophy|ABCA4-related_disorder|not_provided": 1,
    "Cone-rod_dystrophy_3|not_provided": 3,
    "ABCA4-related_disorder|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 1,
    "Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided": 1,
    "not_provided|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 20,
    "Stargardt_disease|Macular_dystrophy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa|Stargardt_disease|Cone-rod_dystrophy": 1,
    "Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|not_provided": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease|Retinal_dystrophy|not_provided": 1,
    "ABCA4-related_retinopathy|Retinitis_Pigmentosa|_Recessive|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Optic_atrophy|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration|Cone_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3": 1,
    "Cone-rod_dystrophy|Stargardt_disease|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_3|not_provided|not_specified": 1,
    "ABCA4-related_disorder|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Cone-rod_dystrophy_3|Cone-rod_dystrophy": 1,
    "ABCA4-related_disorder|not_provided|Retinal_dystrophy|not_specified": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Cone_dystrophy": 12,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_19|Age-related_macular_degeneration|Cone-rod_dystrophy_3|ABCA4-related_disorder|Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa|maculopathy": 1,
    "ABCA4-related_disorder|Macular_degeneration|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|Cone-rod_dystrophy_3|not_provided": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy": 1,
    "not_specified|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 3,
    "Retinitis_pigmentosa_19|not_provided|Cone-rod_dystrophy_3|Retinitis_pigmentosa": 1,
    "Macular_dystrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Cone-rod_dystrophy|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Macular_dystrophy": 1,
    "ABCA4-related_retinopathy|not_provided": 3,
    "ABCA4-related_disorder|not_provided|Macular_degeneration|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive": 2,
    "ABCA4-related_disorder|Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|not_provided|Stargardt_disease": 1,
    "Inborn_genetic_diseases|not_provided|Stargardt_Disease|_Recessive|ABCA4-related_disorder|Macular_degeneration|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 1,
    "ABCA4-related_disorder|Macular_dystrophy|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|See_cases": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease|Cone-rod_dystrophy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "not_provided|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3": 2,
    "not_provided|Retinitis_pigmentosa_19|Retinitis_pigmentosa": 1,
    "Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|ABCA4-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_1": 47,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2": 3,
    "not_provided|ABCA4-related_disorder|not_specified": 4,
    "Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease|not_provided|Retinal_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Stargardt_disease|ABCA4-related_disorder": 1,
    "Retinitis_pigmentosa|Stargardt_disease|Retinal_dystrophy|not_provided": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy|not_provided": 2,
    "See_cases|Retinal_dystrophy": 1,
    "Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|not_specified": 1,
    "not_specified|not_provided|Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Cone-Rod_Dystrophy|_Recessive": 1,
    "Stargardt_disease|Retinal_dystrophy": 2,
    "Visual_impairment": 6,
    "ABCA4-related_disorder|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided|Age_related_macular_degeneration_2": 1,
    "not_specified|not_provided|Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 1,
    "ABCA4-related_disorder|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided": 1,
    "Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_19|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa": 2,
    "Age_related_macular_degeneration_2|Stargardt_disease|Retinal_dystrophy": 1,
    "Retinal_disorders|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_specified|ABCA4-related_disorder|not_provided|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|Macular_degeneration": 1,
    "Retinitis_Pigmentosa|_Recessive|Macular_degeneration|not_specified|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided": 1,
    "Cone-rod_dystrophy_3|Retinal_dystrophy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "ABCA4-related_disorder|Mandibulofacial_dysostosis_with_mental_deficiency|Retinal_dystrophy|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease|MACULAR_DEGENERATION|_AGE-RELATED|_2|_SUSCEPTIBILITY_TO": 1,
    "Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|not_provided|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|not_provided": 2,
    "Retinitis_pigmentosa|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "not_specified|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided|Macular_degeneration": 1,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Macular_degeneration|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinal_dystrophy": 36,
    "not_provided|ABCA4-related_disorder|Inborn_genetic_diseases": 1,
    "Macular_degeneration|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder|Stargardt_Disease|_Recessive": 1,
    "not_specified|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_dystrophy|Macular_degeneration": 1,
    "Macular_degeneration|Stargardt_Disease|_Recessive|not_provided|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive": 1,
    "not_provided|Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 4,
    "Retinitis_pigmentosa_19|Stargardt_disease": 1,
    "Stargardt_Disease|_Recessive|ABCA4-related_disorder|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Macular_degeneration": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "ABCA4-related_disorder|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_provided|Macular_degeneration|Age_related_macular_degeneration_2|ABCA4-related_disorder|Stargardt_Disease|_Recessive": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "Stargardt_Disease|_Recessive|ABCA4-related_disorder|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|not_specified|Macular_degeneration|not_provided": 1,
    "Retinal_dystrophy|not_provided|ABCA4-related_retinopathy": 1,
    "ABCA4-related_retinopathy|ABCA4-related_disorder|not_specified|not_provided|Stargardt_disease|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "not_provided|ABCA4-related_disorder|Retinal_dystrophy": 5,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Macular_degeneration": 1,
    "Inborn_genetic_diseases|not_provided|Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 2,
    "not_provided|Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Cone-Rod_Dystrophy|_Recessive": 1,
    "ABCA4-related_disorder|not_provided|not_specified": 2,
    "Bietti_crystalline_corneoretinal_dystrophy": 23,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|not_provided|Autosomal_recessive_retinitis_pigmentosa|Cone-rod_dystrophy|Stargardt_disease": 1,
    "not_specified|Retinal_dystrophy|not_provided": 14,
    "Retinal_dystrophy|not_provided|ABCA4-related_disorder": 3,
    "Cone-rod_dystrophy|not_provided": 19,
    "ABCA4-related_disorder|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|not_provided|Stargardt_disease": 1,
    "ABCA4-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|Retinal_dystrophy|Stargardt_disease": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|not_provided": 1,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Macular_degeneration|not_provided|not_specified": 1,
    "not_provided|Cone-rod_dystrophy_3": 3,
    "Severe_early-childhood-onset_retinal_dystrophy|Congenital_stationary_night_blindness": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Abnormality_of_the_eye": 1,
    "not_specified|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "ABCA4-related_disorder|Retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder|Bietti_crystalline_corneoretinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Cone_dystrophy": 1,
    "Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|ABCA4-related_disorder": 1,
    "Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Macular_dystrophy|ABCA4-related_disorder|Optic_atrophy|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|not_specified|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|not_provided|Stargardt_disease": 1,
    "ABCA4-related_disorder|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "ABCA4-related_disorder|Retinitis_pigmentosa|not_provided|Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_3": 2,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|not_provided|Stargardt_disease": 1,
    "Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_provided|Macular_degeneration": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|not_specified": 1,
    "ABCA4-related_disorder|Macular_dystrophy|Optic_atrophy|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided|Macular_degeneration": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "not_provided|ABCA4-related_retinopathy|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 1,
    "not_provided|not_specified|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 1,
    "Stargardt_disease_3|not_provided": 8,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa|Cone-rod_dystrophy|Macular_dystrophy|not_provided|Stargardt_disease|Stargardt_disease_3": 1,
    "ABCA4-related_disorder|Retinal_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease_3": 1,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Macular_degeneration": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa|ABCA4-related_disorder|not_provided|Isolated_macular_dystrophy": 1,
    "not_provided|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Stargardt_disease|Optic_atrophy|Retinal_dystrophy": 1,
    "Cone-Rod_Dystrophy|_Recessive|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|ABCA4-related_retinopathy|ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided|Age_related_macular_degeneration_2|Stargardt_disease|MACULAR_DEGENERATION|_AGE-RELATED|_2|_SUSCEPTIBILITY_TO|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease_3|Macular_degeneration": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "Cone-rod_dystrophy_3|ABCA4-related_disorder|Retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided": 1,
    "not_specified|Retinal_dystrophy": 21,
    "Stargardt_disease|ABCA4-related_disorder|Retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|not_specified": 1,
    "Stargardt_disease_3|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19": 1,
    "ABCA4-related_disorder|not_provided|Stargardt_disease|Cone-rod_dystrophy": 1,
    "not_provided|Generalized_choriocapillaris_dystrophy": 2,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Age_related_macular_degeneration_2|Macular_degeneration": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19": 2,
    "not_specified|Macular_degeneration|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Cone-Rod_Dystrophy|_Recessive": 1,
    "Isolated_macular_dystrophy": 6,
    "Cone-rod_dystrophy_3|Retinitis_pigmentosa": 1,
    "Age-related_macular_degeneration|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|ABCA4-related_disorder|Retinal_disorders|Retinal_dystrophy|Inborn_genetic_diseases|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|not_provided|Retinitis_pigmentosa|Stargardt_disease|Cone-rod_dystrophy|Stargardt_disease_3|Abnormal_macular_morphology|Peripheral_neuropathy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided": 2,
    "Retinitis_pigmentosa_19|not_provided": 3,
    "Retinal_dystrophy|not_provided|Stargardt_disease_3": 2,
    "not_provided|not_specified|Retinal_dystrophy": 22,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease|Retinal_dystrophy": 1,
    "Optic_atrophy|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 31,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_3": 1,
    "Retinitis_pigmentosa|not_provided|ABCA4-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 1,
    "Stargardt_disease|Cone-rod_dystrophy_3|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Stargardt_disease": 2,
    "Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "Stargardt_disease|not_provided|ABCA4-related_disorder": 1,
    "not_provided|Stargardt_Disease|_Recessive|ABCA4-related_disorder|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "not_provided|Retinal_dystrophy|Stargardt_disease_3|Inborn_genetic_diseases": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Retinitis_pigmentosa": 1,
    "ABCA4-related_disorder|Benign_concentric_annular_macular_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Stargardt_disease_3": 1,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|not_provided|Stargardt_disease_3": 1,
    "Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Age_related_macular_degeneration_2|not_provided": 1,
    "not_provided|Stargardt_disease_3": 5,
    "Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Retinal_dystrophy": 1,
    "Cone-rod_dystrophy_3|Stargardt_disease|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinal_dystrophy|ABCA4-related_disorder": 1,
    "ABCA4-related_disorder|not_provided|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Macular_dystrophy|not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Cone_dystrophy_and_rod_monochromatism|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease_3|Retinitis_pigmentosa_19|See_cases": 1,
    "Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|ABCA4-related_disorder|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration": 1,
    "Cone_dystrophy|not_provided": 2,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Stargardt_disease_3|not_provided|Cone-rod_dystrophy_3": 1,
    "ABCA4-related_disorder|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|Age_related_macular_degeneration_2|not_provided|Retinitis_pigmentosa|Stargardt_disease_3|Stargardt_disease": 1,
    "ABCA4-related_retinopathy|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|not_provided|Retinal_dystrophy": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2": 1,
    "Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Retinal_dystrophy": 1,
    "Macular_dystrophy|not_provided|Retinal_dystrophy": 1,
    "Cone-rod_dystrophy_3|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|maculopathy|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 1,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration": 1,
    "Stargardt_Disease|_Recessive|ABCA4-related_disorder|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Macular_degeneration": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|not_specified": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|Stargardt_disease_3|ABCA4-related_disorder": 1,
    "Macular_dystrophy|ABCA4-related_disorder|Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|not_specified|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration": 1,
    "Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|not_provided|Macular_degeneration": 1,
    "Macular_dystrophy|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy": 34,
    "Stargardt_disease_3": 53,
    "Stargardt_disease|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|Macular_degeneration|Stargardt_Disease|_Recessive|ABCA4-related_disorder|not_provided": 1,
    "Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|not_provided|Retinal_dystrophy|Age_related_macular_degeneration_2|ABCA4-related_disorder": 1,
    "Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Macular_degeneration|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_3|Retinal_dystrophy": 1,
    "not_provided|ABCA4-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|ABCA4-related_disorder|not_specified|Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Stargardt_disease": 1,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_provided|Macular_degeneration|Stargardt_Disease|_Recessive": 1,
    "not_provided|not_specified|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|Macular_degeneration": 1,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Stargardt_Disease|_Recessive|not_provided|Macular_degeneration": 1,
    "Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Macular_degeneration": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|not_specified": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease": 1,
    "Stargardt_Disease|_Recessive|ABCA4-related_disorder|Macular_degeneration|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 1,
    "not_specified|Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder|Retinal_dystrophy|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided|Macular_degeneration": 1,
    "Macular_degeneration|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_specified|Retinal_dystrophy|not_provided": 1,
    "Late-onset_cone-rod_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 19,
    "Macular_degeneration|not_provided|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive": 1,
    "not_provided|not_specified|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Macular_degeneration": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19": 1,
    "not_provided|Retinal_dystrophy|_early-onset_severe": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_19|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease_3": 1,
    "Macular_dystrophy": 7,
    "not_provided|Macular_degeneration|Stargardt_Disease|_Recessive|ABCA4-related_disorder|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Cone-Rod_Dystrophy|_Recessive": 1,
    "Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|ABCA4-related_disorder|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Retinal_dystrophy": 1,
    "Macular_dystrophy|Retinal_dystrophy|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Progressive_cone_dystrophy_(without_rod_involvement)|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Stargardt_disease": 1,
    "Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|not_provided": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|Stargardt_disease_3": 1,
    "Retinal_dystrophy|Retinal_disorders|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|not_provided|ABCA4-related_disorder": 1,
    "ABCA4-related_disorder|Inborn_genetic_diseases|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|not_provided": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_19|Stargardt_disease": 1,
    "Inborn_genetic_diseases|not_provided|Macular_degeneration|Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Cone-Rod_Dystrophy|_Recessive": 1,
    "Optic_atrophy|Retinal_dystrophy|Stargardt_disease|ABCA4-related_disorder|not_provided": 1,
    "ABCA4-related_disorder|Macular_dystrophy|Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Cone-rod_dystrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19": 1,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3": 2,
    "Late-onset_cone-rod_dystrophy|not_provided|Retinitis_pigmentosa|ABCA4-related_disorder|Macular_degeneration|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive": 1,
    "Stargardt_disease_3|Cone-rod_dystrophy_3|not_provided": 1,
    "not_provided|Macular_degeneration|Visual_impairment|Retinal_atrophy|Central_scotoma|Age_related_macular_degeneration_2": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 1,
    "not_provided|ABCA4-related_retinopathy|ABCA4-related_disorder": 1,
    "Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|ABCA4-related_disorder|Stargardt_Disease|_Recessive|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|Macular_degeneration|not_provided": 1,
    "Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Stargardt_disease|Stargardt_disease_3": 1,
    "ABCA4-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|not_specified|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|not_provided|Stargardt_disease": 1,
    "Stargardt_disease_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "ABCA4-related_disorder|Retinal_dystrophy|Inborn_genetic_diseases|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Abnormal_retinal_morphology": 1,
    "Isolated_macular_dystrophy|not_provided": 3,
    "ABCA4-related_disorder|Retinal_dystrophy|not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease": 1,
    "Stargardt_disease|not_provided|Age_related_macular_degeneration_2": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|not_provided": 1,
    "Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|Stargardt_Disease|_Recessive|Macular_degeneration": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19": 1,
    "Stargardt_Disease|_Recessive|Retinitis_Pigmentosa|_Recessive|ABCA4-related_disorder|Cone-Rod_Dystrophy|_Recessive|Retinal_dystrophy|not_provided|Macular_degeneration": 1,
    "Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Cone-rod_dystrophy_3|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "Stargardt_disease_3|Retinitis_pigmentosa_19": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Cone-rod_dystrophy_3": 1,
    "not_provided|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy": 2,
    "Retinal_dystrophy|not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Stargardt_disease": 1,
    "ABCA4-related_disorder|Age_related_macular_degeneration_2|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Abnormal_macular_morphology|Peripheral_neuropathy|Abnormal_retinal_morphology": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Stargardt_disease_3": 1,
    "ABCA4-related_disorder|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided|Stargardt_disease": 1,
    "Retinal_dystrophy|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19": 1,
    "Retinal_dystrophy|not_specified|Inborn_genetic_diseases|not_provided": 2,
    "Retinal_dystrophy|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "ABCA4-related_disorder|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_3|Age_related_macular_degeneration_2|Severe_early-childhood-onset_retinal_dystrophy|Retinitis_pigmentosa_19|Retinal_atrophy|Macular_degeneration|Central_scotoma|Visual_impairment|not_provided": 1,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Stargardt_disease_3": 1,
    "Generalized_choriocapillaris_dystrophy": 1,
    "ABCA4-related_disorder|Cone-rod_dystrophy_3|Retinitis_pigmentosa_19|Severe_early-childhood-onset_retinal_dystrophy|Age_related_macular_degeneration_2|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease|Cone-rod_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Abnormality_of_the_eye": 1,
    "ARHGAP29-related_disorder": 20,
    "ARHGAP29-related_disorder|not_provided": 6,
    "Nonsyndromic_cleft_lip_with_or_without_cleft_palate": 4,
    "not_provided|ARHGAP29-related_disorder": 1,
    "ARHGAP29-related_disorder|Cleft_palate": 1,
    "Congenital_bile_acid_synthesis_defect_5|not_provided": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_5|not_specified": 1,
    "ABCD3-related_disorder|not_provided": 2,
    "Congenital_bile_acid_synthesis_defect_5": 2,
    "not_provided|Congenital_bile_acid_synthesis_defect_5": 1,
    "ABCD3-related_disorder": 1,
    "Congenital_myasthenic_syndrome_15": 87,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Congenital_myasthenic_syndrome_15": 3,
    "ALG14-related_disorder|Congenital_myasthenic_syndrome_15|not_provided": 2,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15": 7,
    "Congenital_myasthenic_syndrome_15|not_provided": 2,
    "Congenital_myasthenic_syndrome_15|not_provided|Inborn_genetic_diseases|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15|not_provided": 1,
    "Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15|not_provided|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies": 1,
    "Congenital_myasthenic_syndrome_15|ALG14-related_disorder": 1,
    "not_provided|Congenital_myasthenic_syndrome_15|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies": 1,
    "not_provided|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Congenital_myasthenic_syndrome_15|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy": 1,
    "Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Congenital_myasthenic_syndrome_15|not_provided": 1,
    "ALG14-related_disorder": 3,
    "Congenital_myasthenic_syndrome_15|not_provided|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy": 1,
    "Inborn_genetic_diseases|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Congenital_myasthenic_syndrome_15": 1,
    "Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Congenital_myasthenic_syndrome_15|not_provided|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy": 1,
    "Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|not_provided|Congenital_myasthenic_syndrome_15|Congenital_myopathy|See_cases": 1,
    "Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15": 1,
    "Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15|not_provided": 1,
    "Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|not_provided|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Congenital_myasthenic_syndrome_15": 1,
    "not_specified|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Congenital_myasthenic_syndrome_15|not_provided": 1,
    "not_provided|Congenital_myopathy|not_specified|Congenital_myasthenic_syndrome_15": 1,
    "ALG14-related_disorder|Congenital_myasthenic_syndrome_15|not_specified|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_15": 1,
    "Congenital_myasthenic_syndrome_15|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_15|Inborn_genetic_diseases": 1,
    "Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Inborn_genetic_diseases": 1,
    "ALG14-related_disorder|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Congenital_myasthenic_syndrome_15|not_provided|not_specified": 1,
    "not_provided|Intellectual_developmental_disorder_with_epilepsy|_behavioral_abnormalities|_and_coarse_facies|Myopathy|_epilepsy|_and_progressive_cerebral_atrophy|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_15": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency": 189,
    "not_provided|Dihydropyrimidine_dehydrogenase_deficiency": 20,
    "Dihydropyrimidine_dehydrogenase_deficiency|not_provided": 9,
    "Dihydropyrimidine_dehydrogenase_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency": 5,
    "Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Other": 2,
    "DPYD-related_disorder": 5,
    "Fluorouracil_response": 1,
    "Inborn_genetic_diseases|DPYD-related_disorder|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|Fluorouracil_response|fluorouracil_response_-_Other|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity|tegafur_response_-_Toxicity": 1,
    "not_specified|DPYD-related_disorder": 2,
    "Dihydropyrimidine_dehydrogenase_deficiency|not_specified": 4,
    "not_specified|Dihydropyrimidine_dehydrogenase_deficiency|not_provided": 2,
    "fluorouracil_response_-_Other|Inborn_genetic_diseases|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|DPYD-related_disorder": 1,
    "not_provided|DPYD-related_disorder": 2,
    "DPYD-related_disorder|not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Other|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|DPYD-related_disorder": 1,
    "not_provided|Dihydropyrimidine_dehydrogenase_deficiency|not_specified": 1,
    "not_specified|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|Dihydropyrimidine_dehydrogenase_deficiency|not_provided": 2,
    "Dihydropyrimidine_dehydrogenase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "DPYD-related_disorder|not_provided|Inborn_genetic_diseases|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "not_provided|Dihydropyrimidine_dehydrogenase_deficiency|Inborn_genetic_diseases": 2,
    "DPYD-related_disorder|Inborn_genetic_diseases|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Fluorouracil_response|Dihydropyrimidine_dehydrogenase_deficiency|tegafur_response_-_Toxicity|fluorouracil_response_-_Toxicity|capecitabine_response_-_Toxicity|fluorouracil_response_-_Other": 1,
    "Inborn_genetic_diseases|not_provided|Dihydropyrimidine_dehydrogenase_deficiency": 4,
    "not_specified|not_provided|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "not_specified|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Other|fluorouracil_response_-_Toxicity|not_provided": 1,
    "not_provided|Dihydropyrimidine_dehydrogenase_deficiency|DPYD-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Other|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity|tegafur_response_-_Toxicity": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|not_provided|DPYD-related_disorder": 1,
    "DPYD-related_disorder|not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Toxicity|capecitabine_response_-_Toxicity": 1,
    "DPYD-related_disorder|not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity": 1,
    "Inborn_genetic_diseases|fluorouracil_response_-_Other": 1,
    "Inborn_genetic_diseases|Dihydropyrimidine_dehydrogenase_deficiency": 3,
    "Dihydropyrimidine_dehydrogenase_deficiency|DPYD-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DPYD-related_disorder|Dihydropyrimidine_dehydrogenase_deficiency": 2,
    "Neurodevelopmental_delay|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|not_specified|not_provided": 2,
    "DPYD-related_disorder|not_provided|Dihydropyrimidine_dehydrogenase_deficiency": 2,
    "not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Toxicity|capecitabine_response_-_Toxicity": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Other|fluorouracil_response_-_Toxicity": 1,
    "not_provided|DPYD-related_disorder|fluorouracil_response_-_Other|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity": 1,
    "fluorouracil_response_-_Other": 1,
    "not_provided|not_specified|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "DPYD-related_disorder|Inborn_genetic_diseases": 1,
    "5-fluorouracil_response|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "fluorouracil_response_-_Other|Dihydropyrimidine_dehydrogenase_deficiency": 1,
    "not_specified|Dihydropyrimidine_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "DPYD-related_disorder|not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Other|fluorouracil_response_-_Toxicity": 1,
    "DPYD-related_disorder|not_provided|not_specified|Dihydropyrimidine_dehydrogenase_deficiency|fluorouracil_response_-_Toxicity|capecitabine_response_-_Toxicity": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|DPYD-related_disorder|not_provided": 1,
    "Dihydropyrimidine_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "DPYD-related_disorder|not_provided": 1,
    "not_provided|Dihydropyrimidine_dehydrogenase_deficiency|See_cases": 1,
    "not_specified|not_provided|Dihydropyrimidine_dehydrogenase_deficiency|capecitabine_response_-_Toxicity|fluorouracil_response_-_Toxicity": 1,
    "Glycogen_storage_disease_type_III": 2292,
    "not_provided|not_specified|Glycogen_storage_disease_type_III": 6,
    "Glycogen_storage_disease_IIIb|not_provided|Glycogen_storage_disease_type_III": 1,
    "not_provided|Glycogen_storage_disease_IIIb|AGL-related_disorder|Glycogen_storage_disease_type_III": 1,
    "not_specified|not_provided|Glycogen_storage_disease_type_III": 4,
    "Inborn_genetic_diseases|Glycogen_storage_disease_type_III": 51,
    "AGL-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Glycogen_storage_disease_type_III": 1,
    "AGL-related_disorder": 11,
    "AGL-related_disorder|not_provided|Glycogen_storage_disease_type_III": 5,
    "not_provided|Glycogen_storage_disease_type_III|not_specified": 10,
    "Glycogen_storage_disease_type_III|not_provided": 41,
    "not_provided|Glycogen_storage_disease_type_III": 63,
    "AGL-related_disorder|Glycogen_storage_disease_type_III": 9,
    "Glycogen_storage_disease_type_III|not_specified": 21,
    "not_specified|Glycogen_storage_disease_type_III|not_provided": 4,
    "Glycogen_storage_disease_type_III|AGL-related_disorder": 6,
    "Glycogen_storage_disease_type_III|Inborn_genetic_diseases": 59,
    "Glycogen_storage_disease_type_III|not_specified|not_provided": 8,
    "Glycogen_storage_disease_IIIa|not_provided|Glycogen_storage_disease_type_III": 5,
    "Glycogen_storage_disease_type_III|AGL-related_disorder|not_specified": 1,
    "not_specified|Glycogen_storage_disease_type_III|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_type_III": 7,
    "AGL-related_disorder|not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_type_III|not_specified": 1,
    "not_specified|Glycogen_storage_disease_type_III": 17,
    "Glycogen_storage_disease_type_III|Inborn_genetic_diseases|not_provided": 4,
    "Glycogen_storage_disease_type_III|Glycogen_storage_disease_IIIa": 2,
    "Meniere_disease|Glycogen_storage_disease_type_III": 1,
    "Glycogen_storage_disease_IIIa": 6,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_type_III|Meniere_disease": 1,
    "not_provided|Glycogen_storage_disease_type_III|Inborn_genetic_diseases": 8,
    "AGL-related_disorder|Glycogen_storage_disease_type_III|not_provided": 3,
    "Inborn_genetic_diseases|Glycogen_storage_disease_type_III|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_type_III|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_type_III": 2,
    "Glycogen_storage_disease_type_III|not_provided|Glycogen_storage_disease_IIIa": 1,
    "not_specified|not_provided|Glycogen_storage_disease_type_III|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disease_type_III|not_provided|AGL-related_disorder|not_specified": 1,
    "Abnormality_of_metabolism/homeostasis": 12,
    "AGL-related_disorder|not_specified|Glycogen_storage_disease_type_III": 3,
    "Glycogen_storage_disease_IIIa|Glycogen_storage_disease_type_III": 2,
    "AGL-related_disorder|Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_type_III": 1,
    "Glycogen_storage_disease_IIIb": 1,
    "Glycogen_storage_disease_IIIb|Glycogen_storage_disease_IIIa|not_provided|Glycogen_storage_disease_type_III": 1,
    "Glycogen_storage_disease_type_III|not_provided|not_specified": 3,
    "Glycogen_storage_disease_type_III|not_provided|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disease_type_III|not_provided|AGL-related_disorder": 1,
    "AGL-related_disorder|Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_type_III|not_specified": 1,
    "not_provided|AGL-related_disorder|Glycogen_storage_disease_type_III": 1,
    "Glycogen_storage_disease_type_III|AGL-related_disorder|not_provided": 2,
    "AGL-related_disorder|not_specified|not_provided|Glycogen_storage_disease_type_III": 1,
    "not_provided|AGL-related_disorder": 1,
    "Glycogen_storage_disease_type_III|AGL-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Glycogen_storage_disease_IIIc": 1,
    "Inborn_genetic_diseases|Meniere_disease|Glycogen_storage_disease_type_III": 1,
    "AGL-related_disorder|Glycogen_storage_disease_type_III|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_type_III|Meniere_disease|not_provided": 1,
    "Glycogen_storage_disease_IIIb|Glycogen_storage_disease_type_III|not_provided": 1,
    "AGL-related_disorder|not_provided|Glycogen_storage_disease_IIIa|Glycogen_storage_disease_type_III|Glycogen_storage_disease_IIIb": 1,
    "not_provided|AGL-related_disorder|Inborn_genetic_diseases|Glycogen_storage_disease_type_III": 1,
    "AGL-related_disorder|Glycogen_storage_disease_IIIa|not_provided|Glycogen_storage_disease_type_III": 1,
    "Glycogen_storage_disease|Glycogen_storage_disease_type_III": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IIIa|Glycogen_storage_disease_type_III": 1,
    "not_provided|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|SLC35A3-related_disorder": 1,
    "Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 250,
    "Arthrogryposis_multiplex_congenita|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 4,
    "Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|Arthrogryposis_multiplex_congenita": 4,
    "Inborn_genetic_diseases|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 4,
    "not_provided|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|Arthrogryposis_multiplex_congenita": 1,
    "Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|Arthrogryposis_multiplex_congenita|SLC35A3-related_disorder": 1,
    "not_specified|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 3,
    "Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 1,
    "Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|not_provided": 4,
    "Arthrogryposis_multiplex_congenita|not_provided|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 1,
    "SLC35A3-related_disorder|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 1,
    "Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|not_provided": 1,
    "Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome|SLC35A3-related_disorder": 1,
    "not_provided|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 1,
    "not_provided|SLC35A3-related_disorder|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 1,
    "SLC35A3-related_disorder|Arthrogryposis_multiplex_congenita|Autism_spectrum_disorder_-_epilepsy_-_arthrogryposis_syndrome": 1,
    "Microcephaly_14|_primary|_autosomal_recessive": 7,
    "not_specified|Microcephaly_14|_primary|_autosomal_recessive|not_provided": 2,
    "Inborn_genetic_diseases|Microcephaly_14|_primary|_autosomal_recessive": 1,
    "SASS6-related_disorder|not_provided": 1,
    "not_provided|Microcephaly_14|_primary|_autosomal_recessive|not_specified": 2,
    "SASS6-related_disorder|Inborn_genetic_diseases": 1,
    "SASS6-related_disorder": 2,
    "not_provided|Microcephaly_14|_primary|_autosomal_recessive": 1,
    "SASS6-related_disorder|Microcephaly_14|_primary|_autosomal_recessive|not_specified|not_provided": 1,
    "Maple_syrup_urine_disease": 1454,
    "Maple_syrup_urine_disease|not_provided": 38,
    "not_provided|Maple_syrup_urine_disease": 45,
    "Maple_syrup_urine_disease_type_1A": 85,
    "Maple_syrup_urine_disease_type_2": 20,
    "DBT-related_disorder|not_provided|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_1A|not_provided|Maple_syrup_urine_disease": 4,
    "Maple_syrup_urine_disease|Inborn_genetic_diseases": 17,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_2": 7,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A": 52,
    "not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 21,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 59,
    "not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease": 1,
    "DBT-related_disorder": 3,
    "Maple_syrup_urine_disease_type_1A|DBT-related_disorder|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|DBT-related_disorder": 1,
    "not_specified|Maple_syrup_urine_disease": 15,
    "DBT-related_disorder|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease|DBT-related_disorder": 3,
    "Maple_syrup_urine_disease|not_provided|not_specified": 4,
    "Maple_syrup_urine_disease|not_specified|Inborn_genetic_diseases|DBT-related_disorder": 1,
    "Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease": 4,
    "not_specified|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 4,
    "Maple_syrup_urine_disease|not_specified": 15,
    "not_provided|not_specified|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease|not_specified|Maple_syrup_urine_disease_type_1A|not_provided": 2,
    "not_specified|Maple_syrup_urine_disease|not_provided": 3,
    "Maple_syrup_urine_disease_type_2|not_specified|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_2": 1,
    "Maple_syrup_urine_disease|not_provided|Maple_syrup_urine_disease_type_1A|not_specified": 2,
    "not_specified|Maple_syrup_urine_disease|DBT-related_disorder": 1,
    "Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease|not_specified|not_provided|Maple_syrup_urine_disease_type_1A": 1,
    "Maple_syrup_urine_disease|DBT-related_disorder|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_2": 1,
    "Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_provided": 1,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease": 27,
    "Maple_syrup_urine_disease_type_2|not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease|not_specified": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_2|not_provided": 1,
    "Maple_syrup_urine_disease_type_1A|not_specified|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_2|not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|See_cases": 1,
    "Maple_syrup_urine_disease_type_2|not_provided": 1,
    "not_specified|not_provided|Maple_syrup_urine_disease": 6,
    "not_specified|not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_2": 1,
    "Maple_syrup_urine_disease|Inborn_genetic_diseases|not_provided": 2,
    "Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease_type_1A": 1,
    "Maple_syrup_urine_disease|not_provided|Maple_syrup_urine_disease_type_1A": 3,
    "not_provided|DBT-related_disorder|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "not_provided|Maple_syrup_urine_disease_type_2": 2,
    "DBT-related_disorder|not_specified|not_provided|Maple_syrup_urine_disease": 1,
    "not_provided|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A": 8,
    "not_provided|Maple_syrup_urine_disease|not_specified": 4,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_provided": 6,
    "not_provided|Maple_syrup_urine_disease_type_2|Maple_syrup_urine_disease": 1,
    "DBT-related_disorder|Maple_syrup_urine_disease|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_32|not_provided": 3,
    "CDC14A-related_disorder": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_32": 5,
    "not_provided|not_specified|CDC14A-related_disorder": 3,
    "CDC14A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_32|not_specified|CDC14A-related_disorder": 1,
    "not_specified|CDC14A-related_disorder|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_32": 5,
    "not_provided|CDC14A-related_disorder": 2,
    "Ear_malformation|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_32": 1,
    "CDC14A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_32|Ear_malformation": 1,
    "not_provided|CDC14A-related_disorder|not_specified": 1,
    "not_specified|CDC14A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Chorea|_childhood-onset|_with_psychomotor_retardation": 1,
    "Chorea|_childhood-onset|_with_psychomotor_retardation": 1,
    "not_provided|GPR88-related_disorder": 1,
    "Ziegler-Huang_syndrome|Decreased_testicular_size": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 7,
    "Joubert_syndrome_1": 43,
    "Ziegler-Huang_syndrome|Testicular_atrophy": 1,
    "Ziegler-Huang_syndrome": 1,
    "Neurodevelopmental_disorder_with_short_stature|_prominent_forehead|_and_feeding_difficulties": 6,
    "Neurodevelopmental_disorder_with_short_stature|_prominent_forehead|_and_feeding_difficulties|DPH5-related_diphthamide-deficiency_syndrome": 2,
    "Neurodevelopmental_disorder_with_short_stature|_prominent_forehead|_and_feeding_difficulties|not_specified": 1,
    "Strabismus|_susceptibility_to": 1,
    "Fibrochondrogenesis_1|Stickler_syndrome_type_2": 21,
    "Stickler_syndrome_type_2|Fibrochondrogenesis_1": 20,
    "Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_provided": 18,
    "not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 5,
    "Stickler_syndrome_type_2|not_provided|Fibrochondrogenesis_1": 10,
    "Stickler_syndrome_type_2|Fibrochondrogenesis_1|not_provided": 9,
    "Marshall_syndrome|not_provided|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1": 3,
    "Stickler_syndrome_type_2|not_provided|not_specified|Fibrochondrogenesis_1": 1,
    "not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Intervertebral_disc_disorder": 1,
    "not_provided|COL11A1-related_disorder": 36,
    "Fibrochondrogenesis_1|not_provided": 1,
    "Fibrochondrogenesis_1|not_provided|Stickler_syndrome_type_2|Retinal_dystrophy": 1,
    "Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Marshall_syndrome|Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_provided": 1,
    "not_provided|Connective_tissue_disorder|Fibrochondrogenesis_1|Stickler_syndrome_type_2|COL11A1-related_disorder|Marshall_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Stickler_syndrome_type_2": 1,
    "Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Stickler_syndrome_type_2|Fibrochondrogenesis_1|Marshall_syndrome": 1,
    "Stickler_syndrome_type_2": 45,
    "Marshall_syndrome|Stickler_syndrome_type_2|Fibrochondrogenesis_1|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss": 11,
    "not_provided|Stickler_syndrome_type_2|Connective_tissue_disorder|Fibrochondrogenesis_1|not_specified": 1,
    "Fibrochondrogenesis_1": 4,
    "not_provided|Hearing_loss|_autosomal_dominant_37|Stickler_syndrome_type_2|Marshall_syndrome": 1,
    "not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1": 5,
    "Stickler_syndrome_type_2|Intervertebral_disc_disorder|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Fibrochondrogenesis_1|COL11A1-related_disorder|Inborn_genetic_diseases|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis_1|Marshall_syndrome|Stickler_syndrome_type_2|not_specified": 3,
    "COL11A1-related_disorder|not_provided": 31,
    "Stickler_syndrome_type_2|Fibrochondrogenesis_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Fibrochondrogenesis_1|Inborn_genetic_diseases": 1,
    "COL11A1-related_disorder|Marshall_syndrome|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Fibrochondrogenesis_1|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_37|Inborn_genetic_diseases|not_provided": 1,
    "COL11A1-related_disorder": 43,
    "not_specified|not_provided|COL11A1-related_disorder": 2,
    "Connective_tissue_disorder|not_specified|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 4,
    "Lumbar_disk_herniation|_susceptibility_to|not_specified|Marshall_syndrome|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Connective_tissue_disorder|Fibrochondrogenesis_1|not_provided": 1,
    "Meniere_disease|Stickler_syndrome_type_2|Fibrochondrogenesis_1|not_provided": 1,
    "Marshall_syndrome": 13,
    "Stickler_syndrome_type_2|not_provided|Neurodevelopmental_disorder": 1,
    "Stickler_syndrome_type_2|Marshall_syndrome|not_provided|Hearing_loss|_autosomal_dominant_37|COL11A1-related_disorder": 1,
    "Stickler_syndrome_type_2|not_provided": 5,
    "Marshall_syndrome|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37": 1,
    "not_provided|Inborn_genetic_diseases|COL11A1-related_disorder": 2,
    "not_provided|Stickler_syndrome_type_2|COL11A1-related_disorder|Fibrochondrogenesis_1": 1,
    "not_provided|Inborn_genetic_diseases|Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_specified": 1,
    "Hearing_loss|_autosomal_dominant_37|not_provided": 3,
    "COL11A1-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "not_provided|Stickler_syndrome_type_2": 10,
    "not_provided|Marshall_syndrome|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1": 1,
    "Hearing_loss|_autosomal_dominant_37": 14,
    "not_provided|not_specified|Marshall_syndrome|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1": 1,
    "not_provided|Hearing_impairment|Hearing_loss|_autosomal_dominant_37": 1,
    "not_provided|Autosomal_recessive_Stickler_syndrome|Stickler_syndrome_type_2|Marshall_syndrome|Fibrochondrogenesis": 1,
    "COL11A1-related_disorder|Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Intervertebral_disc_disorder|Stickler_syndrome_type_2|Inborn_genetic_diseases|not_provided": 1,
    "COL11A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Fibrochondrogenesis_1|Marshall_syndrome|Intervertebral_disc_disorder|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37": 1,
    "not_specified|Intervertebral_disc_disorder|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "Stickler_syndrome_type_2|not_provided|Fibrochondrogenesis_1|not_specified": 3,
    "Connective_tissue_disorder|not_provided|Stickler_syndrome_type_2|not_specified|Fibrochondrogenesis_1": 1,
    "Stickler_syndrome_type_2|Fibrochondrogenesis_1|COL11A1-related_disorder|not_provided": 1,
    "not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1|Intervertebral_disc_disorder|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37": 1,
    "Myopia|Abnormal_facial_shape|Hypertelorism|Telecanthus|Short_nose|Cleft_palate|Megalocornea|Hypoplasia_of_the_maxilla": 1,
    "COL11A1-related_disorder|Inborn_genetic_diseases|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "not_provided|Marshall_syndrome|Stickler_syndrome_type_2|Intervertebral_disc_disorder|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis_1": 2,
    "Connective_tissue_disorder|not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1": 1,
    "not_specified|not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1": 1,
    "Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2|not_provided|not_specified": 1,
    "Fibrochondrogenesis|not_provided": 2,
    "Connective_tissue_disorder|not_provided|not_specified": 9,
    "Inborn_genetic_diseases|not_provided|COL11A1-related_disorder": 1,
    "Stickler_syndrome_type_2|Marshall_syndrome|not_specified|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis_1|not_provided": 1,
    "not_specified|Marshall_syndrome|not_provided|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1": 1,
    "Marshall_syndrome|not_provided|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1|not_specified": 1,
    "not_provided|Marshall_syndrome": 3,
    "not_provided|Stickler_syndrome_type_2|Marshall_syndrome|Fibrochondrogenesis_1": 1,
    "Marshall_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|COL11A1-related_disorder|not_provided|Stickler_syndrome_type_2|Marshall_syndrome": 1,
    "Fibrochondrogenesis_1|Stickler_syndrome_type_2|Marshall_syndrome|not_specified|not_provided": 1,
    "COL11A1-related_disorder|Marshall_syndrome|Intervertebral_disc_disorder|Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Stickler_syndrome_type_2|not_provided": 1,
    "Stickler_syndrome_type_2|Fibrochondrogenesis_1|not_provided|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Intervertebral_disc_disorder|Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_provided": 1,
    "not_specified|Stickler_syndrome_type_2|not_provided|Fibrochondrogenesis_1": 1,
    "Osteogenesis_imperfecta_type_III": 67,
    "not_provided|Fibrochondrogenesis_1": 1,
    "Stickler_syndrome_type_2|Marshall_syndrome": 2,
    "COL11A1-related_disorder|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 2,
    "not_specified|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "not_provided|not_specified|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis_1|Marshall_syndrome|Stickler_syndrome_type_2": 1,
    "Fibrochondrogenesis_1|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Stickler_syndrome_type_2|not_provided": 1,
    "not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Fibrochondrogenesis_1|Stickler_syndrome_type_2|Connective_tissue_disorder": 1,
    "not_provided|Fibrochondrogenesis|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Stickler_syndrome|Marshall_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_37|not_specified|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "COL11A1-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2": 3,
    "not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_specified": 2,
    "Marshall_syndrome|Stickler_syndrome_type_2|not_provided": 1,
    "Fibrochondrogenesis_1|Intervertebral_disc_disorder|Stickler_syndrome_type_2|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|COL11A1-related_disorder|not_provided": 1,
    "Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2|not_specified|not_provided": 2,
    "not_specified|Fibrochondrogenesis_1|not_provided|Stickler_syndrome_type_2": 1,
    "Marshall/Stickler_syndrome": 1,
    "COL11A1-related_disorder|Connective_tissue_disorder|not_specified|not_provided": 2,
    "Stickler_syndrome_type_2|not_provided|COL11A1-related_disorder": 1,
    "Stickler_syndrome_type_2|not_provided|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome": 1,
    "Marshall_syndrome|Stickler_syndrome_type_2": 1,
    "Retinal_dystrophy|Stickler_syndrome_type_2": 1,
    "Stickler_syndrome_type_2|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis_1|not_provided": 1,
    "Autism|Neurodevelopmental_delay": 1,
    "Hearing_loss|_autosomal_dominant_37|Stickler_syndrome_type_2|Marshall_syndrome": 1,
    "Marshall_syndrome|Inborn_genetic_diseases|not_provided|Fibrochondrogenesis_1": 1,
    "Inborn_genetic_diseases|Fibrochondrogenesis_1|Marshall_syndrome|Stickler_syndrome_type_2|not_provided": 1,
    "Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Marshall_syndrome|Stickler_syndrome_type_2|not_specified|not_provided": 2,
    "not_provided|Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2|not_specified": 1,
    "Connective_tissue_disorder|not_provided|COL11A1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hearing_impairment": 5,
    "Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Stickler_syndrome_type_2|Marshall_syndrome|not_provided": 1,
    "not_provided|Marshall_syndrome|Fibrochondrogenesis_1|Intervertebral_disc_disorder|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37": 1,
    "Fibrochondrogenesis_1|not_provided|Inborn_genetic_diseases|Stickler_syndrome_type_2": 1,
    "Inborn_genetic_diseases|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "Retinal_dystrophy|Hearing_loss|_autosomal_dominant_37|not_provided": 1,
    "Fibrochondrogenesis_1|not_provided|Stickler_syndrome_type_2": 1,
    "Fibrochondrogenesis": 2,
    "COL11A1-related_disorder|not_specified|not_provided": 1,
    "not_specified|COL11A1-related_disorder|not_provided": 2,
    "Marshall_syndrome|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis_1|Intervertebral_disc_disorder|not_provided": 1,
    "Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Fibrochondrogenesis_1|Intervertebral_disc_disorder|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2|Fibrochondrogenesis_1|Intervertebral_disc_disorder": 1,
    "Meniere_disease|Hearing_loss|_autosomal_dominant_37|not_provided": 1,
    "not_provided|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Fibrochondrogenesis_1|Intervertebral_disc_disorder": 1,
    "Intervertebral_disc_disorder": 1,
    "not_specified|Fibrochondrogenesis_1|Connective_tissue_disorder|Stickler_syndrome_type_2|not_provided": 1,
    "Stickler_syndrome_type_2|Intervertebral_disc_disorder|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Fibrochondrogenesis_1|not_provided": 1,
    "Hearing_impairment|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|Fibrochondrogenesis_1|Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2|not_provided": 1,
    "Stickler_syndrome_type_2|Marshall_syndrome|COL11A1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Connective_tissue_disorder": 6,
    "not_provided|not_specified|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "Fibrochondrogenesis_1|Stickler_syndrome_type_2|COL11A1-related_disorder|not_provided": 2,
    "COL11A1-related_disorder|not_provided|Stickler_syndrome_type_2|Fibrochondrogenesis_1": 1,
    "Short_stature|not_provided": 1,
    "Connective_tissue_disorder|Stickler_syndrome_type_2|not_specified|not_provided|Fibrochondrogenesis_1": 1,
    "Fibrochondrogenesis_1|Connective_tissue_disorder|not_provided|Stickler_Syndrome|_Dominant|Marshall_syndrome|not_specified": 1,
    "Marshall_syndrome|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1|not_provided": 1,
    "Stickler_syndrome_type_2|Marshall_syndrome|not_provided|Hearing_loss|_autosomal_dominant_37|not_specified|Fibrochondrogenesis_1": 1,
    "Marshall_syndrome|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1|not_specified|not_provided": 1,
    "Stickler_syndrome_type_2|COL11A1-related_disorder": 1,
    "Stickler_syndrome_type_2|Inborn_genetic_diseases|Stickler_syndrome|not_provided": 1,
    "Stickler_syndrome_type_2|not_provided|Connective_tissue_disorder|Fibrochondrogenesis_1": 1,
    "Connective_tissue_disorder|not_provided|Inborn_genetic_diseases": 2,
    "COL11A1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Stickler_syndrome_type_2|COL11A1-related_disorder|Meniere_disease|Fibrochondrogenesis_1": 1,
    "not_provided|CHEK2-related_cancer_predisposition": 1,
    "Hearing_loss|_autosomal_dominant_37|Marshall_syndrome|Stickler_syndrome_type_2": 1,
    "Childhood_onset_hearing_loss": 7,
    "COL11A1-related_disorder|not_specified|not_provided|Connective_tissue_disorder": 1,
    "Fibrochondrogenesis_1|Stickler_syndrome": 1,
    "COL11A1-related_disorder|Marshall_syndrome|Fibrochondrogenesis_1|Intervertebral_disc_disorder|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|not_provided": 1,
    "COL11A1-related_disorder|Inborn_genetic_diseases": 1,
    "Fibrochondrogenesis_1|Marshall_syndrome|Stickler_syndrome_type_2": 1,
    "not_provided|Childhood_onset_hearing_loss": 3,
    "COL11A1-related_disorder|not_specified|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "not_provided|not_specified|COL11A1-related_disorder": 1,
    "not_provided|not_specified|Stickler_syndrome_type_2|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|Fibrochondrogenesis_1|Marshall_syndrome|COL11A1-related_disorder": 1,
    "Inborn_genetic_diseases|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Fibrochondrogenesis|Stickler_syndrome_type_2|not_specified|not_provided": 1,
    "Connective_tissue_disorder|Stickler_syndrome_type_2|Fibrochondrogenesis_1|not_provided|not_specified": 1,
    "Stickler_syndrome_type_2|Connective_tissue_disorder|Fibrochondrogenesis_1|not_provided|not_specified": 1,
    "Fibrochondrogenesis_1|COL11A1-related_disorder|not_provided": 1,
    "Stickler_syndrome_type_2|not_provided|Fibrochondrogenesis_1|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "sporadic_abdominal_aortic_aneurysm": 1,
    "Stickler_syndrome_type_2|not_provided|Connective_tissue_disorder|Meniere_disease|Fibrochondrogenesis_1|not_specified": 1,
    "Stickler_syndrome_type_2|not_specified|not_provided|Fibrochondrogenesis_1": 1,
    "Hearing_loss|_autosomal_dominant_37|Hearing_impairment|not_provided": 1,
    "Stickler_Syndrome|_Dominant|Connective_tissue_disorder|not_specified|not_provided|Fibrochondrogenesis_1|Marshall_syndrome": 1,
    "Marshall_syndrome|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1|not_provided|not_specified": 1,
    "Hearing_loss|_autosomal_dominant_37|Stickler_syndrome_type_2|not_provided|Fibrochondrogenesis_1|not_specified|Connective_tissue_disorder|Marshall_syndrome": 1,
    "not_specified|Connective_tissue_disorder|Fibrochondrogenesis_1|not_provided|Stickler_Syndrome|_Dominant|Marshall_syndrome": 1,
    "Inborn_genetic_diseases|Fibrochondrogenesis_1|not_provided|Stickler_syndrome_type_2|not_specified": 1,
    "not_provided|Fibrochondrogenesis_1|Intervertebral_disc_disorder|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Stickler_syndrome_type_2": 1,
    "COL11A1-related_disorder|Fibrochondrogenesis_1|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_37": 1,
    "Stickler_syndrome_type_2|not_provided|Fibrochondrogenesis_1|COL11A1-related_disorder": 1,
    "Marfan_syndrome": 1215,
    "COL11A1-related_disorder|Connective_tissue_disorder|Meniere_disease|not_specified|not_provided|Fibrochondrogenesis_1|Stickler_syndrome_type_2": 1,
    "Stickler_syndrome_type_2|COL11A1-related_disorder|Fibrochondrogenesis_1|not_provided": 1,
    "Marshall_syndrome|Fibrochondrogenesis_1|Stickler_syndrome_type_2|not_specified|not_provided|COL11A1-related_disorder": 1,
    "not_provided|Stickler_syndrome_type_2|Marshall_syndrome": 1,
    "not_provided|Skeletal_dysplasia|Stickler_syndrome_type_2|Fibrochondrogenesis_1": 1,
    "not_provided|Fibrochondrogenesis_1|not_specified|Stickler_syndrome_type_2": 1,
    "not_specified|Stickler_syndrome_type_2|Connective_tissue_disorder|Fibrochondrogenesis_1|Marshall_syndrome|Hearing_loss|_autosomal_dominant_37|Intervertebral_disc_disorder|not_provided": 1,
    "not_specified|Stickler_syndrome_type_2|Fibrochondrogenesis_1": 1,
    "Marshall_syndrome|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_1": 2,
    "Isolated_growth_hormone_deficiency|_type_5": 13,
    "RNPC3-related_disorder": 4,
    "Isolated_growth_hormone_deficiency|_type_5|not_provided": 1,
    "not_provided|Isolated_growth_hormone_deficiency|_type_5": 1,
    "not_provided|Decreased_response_to_growth_hormone_stimulation_test|Isolated_growth_hormone_deficiency|_type_5": 1,
    "Decreased_response_to_growth_hormone_stimulation_test": 17,
    "RNPC3-related_disorder|Isolated_growth_hormone_deficiency|_type_5": 1,
    "Isolated_growth_hormone_deficiency|_type_5|RNPC3-related_disorder": 1,
    "Isolated_growth_hormone_deficiency|_type_5|Decreased_response_to_growth_hormone_stimulation_test": 1,
    "Small_for_gestational_age": 9,
    "PRMT6-related_disorder": 5,
    "not_provided|NTNG1-related_disorder": 3,
    "NTNG1-related_disorder|not_provided": 1,
    "NTNG1-related_disorder": 2,
    "SLC25A24-related_disorder": 7,
    "Fontaine_progeroid_syndrome": 8,
    "Dementia|Bilateral_tonic-clonic_seizure": 2,
    "not_provided|SLC25A24-related_disorder": 2,
    "Fontaine_progeroid_syndrome|not_provided": 4,
    "SLC25A24-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "SLC25A24-related_disorder|not_provided|not_specified": 1,
    "not_specified|Male_infertility": 3,
    "not_specified|High_myopia": 9,
    "Immune_dysregulation|_autoimmunity|_and_autoinflammation": 4,
    "STXBP3-related_disorders": 1,
    "Chudley-McCullough_syndrome": 42,
    "not_specified|Chudley-McCullough_syndrome|not_provided": 3,
    "GPSM2-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Chudley-McCullough_syndrome": 4,
    "Chudley-McCullough_syndrome|not_specified": 2,
    "Chudley-McCullough_syndrome|not_specified|not_provided": 2,
    "GPSM2-related_disorder": 4,
    "not_provided|Chudley-McCullough_syndrome": 7,
    "Chudley-McCullough_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hearing_loss|_autosomal_recessive": 1,
    "Chudley-McCullough_syndrome|not_provided|not_specified": 2,
    "GPSM2-related_disorder|not_provided": 4,
    "not_provided|not_specified|GPSM2-related_disorder|Inborn_genetic_diseases": 1,
    "Chudley-McCullough_syndrome|not_provided": 9,
    "Rare_genetic_deafness|not_provided|Chudley-McCullough_syndrome|GPSM2-related_disorder": 2,
    "not_provided|GPSM2-related_disorder": 1,
    "not_provided|Chudley-McCullough_syndrome|not_specified": 1,
    "Chudley-McCullough_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "not_specified|Chudley-McCullough_syndrome": 2,
    "Rare_genetic_deafness|not_provided": 26,
    "Inborn_genetic_diseases|not_provided|Chudley-McCullough_syndrome": 3,
    "Chudley-McCullough_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Chudley-McCullough_syndrome|Rare_genetic_deafness|GPSM2-related_disorder": 1,
    "not_specified|GPSM2-related_disorder|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|Chudley-McCullough_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Chudley-McCullough_syndrome|not_provided": 1,
    "not_provided|Chudley-McCullough_syndrome|not_specified|GPSM2-related_disorder|Inborn_genetic_diseases": 1,
    "GPSM2-related_disorder|not_provided|not_specified|Chudley-McCullough_syndrome": 1,
    "Hearing_impairment|not_specified": 5,
    "GPSM2-related_disorder|not_specified|not_provided|Chudley-McCullough_syndrome": 1,
    "not_provided|Chudley-McCullough_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Chudley-McCullough_syndrome": 1,
    "Chudley-McCullough_syndrome|not_provided|GPSM2-related_disorder": 1,
    "Retinitis_pigmentosa_32|not_provided": 1,
    "Retinitis_pigmentosa_32|not_provided|not_specified": 1,
    "Retinitis_pigmentosa_32|Retinal_dystrophy|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_60": 4,
    "TAF13-related_disorder": 1,
    "Autosomal_recessive_primary_microcephaly": 16,
    "not_provided|TAF13-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_60": 1,
    "SARS1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_ataxia|_and_seizures|not_provided": 2,
    "SARS1-related_disorder|Neurodevelopmental_disorder_with_microcephaly|_ataxia|_and_seizures|not_specified": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_ataxia|_and_seizures": 7,
    "not_provided|SARS1-related_disorder": 1,
    "SARS1-related_disorder|not_provided": 1,
    "Cerebral_arteriovenous_malformation": 13,
    "not_provided|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 23,
    "not_specified|Neurodevelopmental_disorder_with_microcephaly|_ataxia|_and_seizures": 1,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_provided": 27,
    "CELSR2-related_disorder|not_provided": 13,
    "not_provided|CELSR2-related_disorder": 21,
    "CELSR2-related_disorder": 23,
    "CELSR2-related_disorder|not_specified": 1,
    "Intellectual_disability|Global_developmental_delay": 2,
    "CELSR2-related_disorder|not_provided|Idiopathic_scoliosis": 1,
    "not_provided|Orofacial-digital_syndrome_III": 1,
    "CELSR2-related_disorder|not_provided|not_specified": 1,
    "LOW_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_6": 1,
    "Brugada_syndrome|not_provided": 44,
    "Hypertrophic_cardiomyopathy|not_specified": 321,
    "SORT1-related_disorder": 8,
    "SORT1-related_disorder|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1": 1329,
    "GNAI3-related_disorder": 4,
    "not_provided|GNAI3-related_disorder": 4,
    "not_provided|Auriculocondylar_syndrome_1": 1,
    "Auriculocondylar_syndrome_1": 9,
    "Auriculocondylar_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|GNAI3-related_disorder": 1,
    "Achromatopsia_4": 20,
    "not_provided|Inborn_genetic_diseases|Achromatopsia_4": 2,
    "Inborn_genetic_diseases|Achromatopsia_4|not_provided": 2,
    "not_provided|Achromatopsia_4": 8,
    "not_provided|not_specified|Achromatopsia_4": 1,
    "Achromatopsia_4|not_provided": 13,
    "Achromatopsia_4|not_provided|Cone_dystrophy": 1,
    "Achromatopsia_4|Inborn_genetic_diseases|not_provided": 1,
    "Achromatopsia_4|not_provided|Retinal_dystrophy": 1,
    "Achromatopsia_4|Retinal_dystrophy": 2,
    "Achromatopsia_4|Cone_dystrophy": 1,
    "Achromatopsia": 72,
    "Achromatopsia|Achromatopsia_4": 1,
    "not_specified|Achromatopsia_4|not_provided": 1,
    "Achromatopsia|not_provided|Achromatopsia_4": 1,
    "GNAT2-related_disorder|Retinal_dystrophy|not_specified|not_provided|Achromatopsia_4": 1,
    "not_provided|Achromatopsia_4|not_specified": 2,
    "GNAT2-related_disorder": 1,
    "not_specified|not_provided|Achromatopsia_4": 1,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_provided": 5,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9": 146,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63": 90,
    "not_provided|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9": 5,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|Inborn_genetic_diseases": 9,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_provided|Inborn_genetic_diseases|not_specified|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63": 6,
    "not_provided|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_specified": 1,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|not_specified|not_provided": 2,
    "Hereditary_spastic_paraplegia_63": 7,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9": 4,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|not_provided": 9,
    "Pontocerebellar_hypoplasia_type_9|not_specified|Hereditary_spastic_paraplegia_63|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_9": 19,
    "not_provided|Pontocerebellar_hypoplasia_type_9": 1,
    "AMPD2-related_disorder|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9": 2,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|AMPD2-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_provided|Hereditary_spastic_paraplegia": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_9|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63": 7,
    "Pontocerebellar_hypoplasia_type_9|not_provided": 2,
    "Pontoneocerebellar_hypoplasia|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9": 1,
    "AMPD2-related_disorder|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_provided": 1,
    "AMPD2-related_disorder|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63": 2,
    "AMPD2-related_disorder": 4,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_specified": 2,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|not_specified": 1,
    "AMPD2-related_disorder|Pontocerebellar_hypoplasia_type_9|not_provided|Hereditary_spastic_paraplegia_63": 1,
    "Hereditary_spastic_paraplegia|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_specified|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_9|not_provided|Pontoneocerebellar_hypoplasia": 1,
    "AMPD2-related_disorder|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|Global_developmental_delay|Seizure|Brain_malformation": 1,
    "not_provided|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|AMPD2-related_disorder": 2,
    "AMPD2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|AMPD2-related_disorder|Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63": 1,
    "Pontocerebellar_hypoplasia_type_9|not_provided|Hereditary_spastic_paraplegia_63": 2,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|Pontoneocerebellar_hypoplasia": 1,
    "Pontocerebellar_hypoplasia_type_9|Hereditary_spastic_paraplegia_63|not_provided|Inborn_genetic_diseases": 1,
    "AMPD2-related_disorder|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_9|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_63|not_specified": 1,
    "Inborn_genetic_diseases|AMPD2-related_disorder|not_provided": 1,
    "AMPD2-related_disorder|Hereditary_spastic_paraplegia_63|Pontocerebellar_hypoplasia_type_9|not_provided": 1,
    "GSTM1-related_disorder": 1,
    "EPS8L3-related_disorder|not_provided": 2,
    "not_specified|Hypotrichosis_5": 1,
    "EPS8L3-related_disorder": 1,
    "Hypotrichosis_5": 1,
    "ALX3-related_disorder": 1,
    "Frontorhiny": 9,
    "Frontorhiny|Inborn_genetic_diseases": 1,
    "not_provided|Frontorhiny": 2,
    "ALX3-related_disorder|Inborn_genetic_diseases": 1,
    "ALX3-related_disorder|not_provided": 1,
    "Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome": 14,
    "Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome|not_provided": 2,
    "not_specified|Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome|not_provided": 1,
    "SLC6A17-related_disorder|not_specified": 1,
    "Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome|not_specified|not_provided": 1,
    "not_specified|Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome": 3,
    "not_provided|Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome|not_specified": 1,
    "not_provided|SLC6A17-related_disorder": 1,
    "SLC6A17-related_disorder": 4,
    "not_provided|Progressive_essential_tremor-speech_impairment-facial_dysmorphism-intellectual_disability-abnormal_behavior_syndrome": 1,
    "Congenital_long_QT_syndrome": 311,
    "Developmental_and_epileptic_encephalopathy|_32": 334,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_32": 3,
    "KCNA2-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_32": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_32": 9,
    "Developmental_and_epileptic_encephalopathy|_32|Inborn_genetic_diseases": 6,
    "Developmental_and_epileptic_encephalopathy|_32|not_provided": 24,
    "not_provided|Developmental_and_epileptic_encephalopathy|_32|Seizure": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_32": 16,
    "Inborn_genetic_diseases|not_provided|Seizure|Developmental_and_epileptic_encephalopathy|_32": 1,
    "Developmental_and_epileptic_encephalopathy|_32|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_32|KCN2A-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_32|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_32|not_provided|KCNA2-related_disorder": 1,
    "KCNA2-related_disorder|Developmental_and_epileptic_encephalopathy|_32": 2,
    "KCNA2-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_32": 1,
    "Developmental_and_epileptic_encephalopathy|_32|not_provided|See_cases": 1,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_32": 1,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_32|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_32|not_specified": 1,
    "KCNA2-related_disorder": 3,
    "KCNA2-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_32": 2,
    "Intellectual_disability|Seizure": 7,
    "not_specified|Developmental_and_epileptic_encephalopathy|_32": 2,
    "Seizure|Developmental_and_epileptic_encephalopathy|_32": 1,
    "Developmental_and_epileptic_encephalopathy|_32|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|KCNA2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_32|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_32|not_provided|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_32|Autism_spectrum_disorder": 1,
    "KCNA3-associated_developmental_and_epileptic_encephalopathy": 10,
    "KCNA3-associated_disorder|KCNA3-associated_developmental_and_epileptic_encephalopathy|not_provided": 1,
    "KCNA3-associated_disorder": 1,
    "KCNA3-associated_developmental_and_epileptic_encephalopathy|not_provided": 1,
    "KCNA3-associated_developmental_and_epileptic_encephalopathy|Neurodevelopmental_disorder": 1,
    "KCNA3-related_neurodevelopmental_disorder": 1,
    "KCNA3-related_disorder": 1,
    "Facioscapulohumeral_muscular_dystrophy_3|_digenic": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_21": 1,
    "DRAM2-related_disorder": 3,
    "Cone-rod_dystrophy_21|not_provided": 3,
    "not_provided|Cone-rod_dystrophy_21": 4,
    "Cone-rod_dystrophy_21": 2,
    "Cone-rod_dystrophy_21|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_21|Retinal_dystrophy": 4,
    "End-stage_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_sine_pigmento_with_macular_involvement": 1,
    "DRAM2-related_disorder|not_provided": 1,
    "Preeclampsia": 22,
    "ADORA3-related_disorder": 2,
    "RAP1A-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis": 57,
    "Spinocerebellar_ataxia_type_19/22|not_provided|Cardiovascular_phenotype": 2,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|not_provided": 5,
    "Spinocerebellar_ataxia_type_19/22": 150,
    "Spinocerebellar_ataxia_type_19/22|not_provided|Brugada_syndrome_9": 1,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype": 35,
    "Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22|not_provided": 6,
    "Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22": 33,
    "Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|Brugada_syndrome_9": 2,
    "Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9": 2,
    "Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|not_provided": 3,
    "Spinocerebellar_ataxia_type_19/22|not_provided": 6,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|Brugada_syndrome_9|not_provided": 2,
    "not_provided|Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22|not_provided|Brugada_syndrome_9": 1,
    "not_specified|Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype": 3,
    "Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22": 1,
    "Neurodevelopmental_delay|Cardiovascular_phenotype|not_provided": 1,
    "Brugada_syndrome_9|Spinocerebellar_ataxia_type_19/22": 2,
    "Spinocerebellar_ataxia_type_19/22|not_provided|KCND3-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|not_specified": 1,
    "Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Spinocerebellar_ataxia_type_19/22": 6,
    "KCND3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Spinocerebellar_ataxia_type_19/22": 1,
    "KCND3-related_disorder": 2,
    "not_specified|Spinocerebellar_ataxia_type_19/22|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9": 1,
    "Spinocerebellar_ataxia_type_19/22|not_specified|KCND3-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Spinocerebellar_ataxia_type_19/22|not_provided|KCND3-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9": 1,
    "Spinocerebellar_ataxia_type_19/22|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "not_provided|Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22": 3,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype": 1,
    "not_provided|Spinocerebellar_ataxia_type_19/22|not_specified": 1,
    "Epilepsy": 530,
    "Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|not_provided": 1,
    "Spinocerebellar_ataxia_type_19/22|Variant_of_unknown_significance": 1,
    "not_provided|Spinocerebellar_ataxia_type_19/22": 4,
    "not_provided|Cardiovascular_phenotype|Hereditary_ataxia|Spinocerebellar_ataxia_type_19/22": 1,
    "Variant_of_unknown_significance": 24,
    "Neurodevelopmental_delay|Brugada_syndrome_9|not_provided|Spinocerebellar_ataxia_type_19/22": 1,
    "Spinocerebellar_ataxia_type_19/22|not_specified|not_provided": 1,
    "Hereditary_ataxia|Spinocerebellar_ataxia_type_19/22": 1,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_19/22|not_specified|Cardiovascular_phenotype": 4,
    "Brugada_syndrome": 1542,
    "not_specified|Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Spinocerebellar_ataxia_type_19/22|KCND3-related_disorder": 1,
    "not_specified|Spinocerebellar_ataxia_type_19/22|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|KCND3-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|not_specified": 91,
    "not_specified|Spinocerebellar_ataxia_type_19/22": 1,
    "Spinocerebellar_ataxia_type_19/22|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Spinocerebellar_ataxia_type_19/22|KCND3-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Spinocerebellar_ataxia_type_19/22|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Spinocerebellar_ataxia_type_19/22": 1,
    "KCND3-related_disorder|Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Spinocerebellar_ataxia_type_19/22": 1,
    "Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_19/22|Cardiovascular_phenotype|not_provided|KCND3-related_disorder": 1,
    "Spinocerebellar_ataxia_type_19/22|not_provided|Brugada_syndrome_9|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Spinocerebellar_ataxia_type_19/22|KCND3-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Spinocerebellar_ataxia_type_19/22": 1,
    "Diarrhea_9": 2,
    "Failure_to_thrive_in_infancy|Diarrhea|Impaired_feeding_ability|Chronic_diarrhea|Failure_to_thrive|Diarrhea_9": 1,
    "WNT2B-related_disorder|not_provided": 3,
    "Diarrhea_9|not_specified": 1,
    "Diarrhea_9|not_provided": 3,
    "not_provided|WNT2B-related_disorder": 3,
    "MOV10-related_disorder": 3,
    "not_provided|Exercise-induced_hyperinsulinism": 10,
    "Exercise-induced_hyperinsulinism": 55,
    "Hyperinsulinism|_Dominant|not_provided": 1,
    "Hyperinsulinism|_Dominant": 12,
    "not_specified|not_provided|Metabolic_myopathy_due_to_lactate_transporter_defect|Exercise-induced_hyperinsulinism|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency": 1,
    "Metabolic_myopathy_due_to_lactate_transporter_defect|not_provided|not_specified": 1,
    "not_provided|not_specified|Exercise-induced_hyperinsulinism": 1,
    "Exercise-induced_hyperinsulinism|not_provided": 2,
    "SLC16A1-related_disorder": 7,
    "Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Exercise-induced_hyperinsulinism": 1,
    "Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency|Exercise-induced_hyperinsulinism": 1,
    "SLC16A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Exercise-induced_hyperinsulinism": 1,
    "Monocarboxylate_transporter_1_deficiency|_autosomal_recessive|Exercise-induced_hyperinsulinism": 1,
    "not_provided|Inborn_genetic_diseases|Exercise-induced_hyperinsulinism": 1,
    "Metabolic_myopathy_due_to_lactate_transporter_defect|Exercise-induced_hyperinsulinism|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency|SLC16A1-related_disorder|not_provided": 1,
    "Monocarboxylate_transporter_1_deficiency|_autosomal_dominant": 2,
    "Monocarboxylate_transporter_1_deficiency|_autosomal_recessive|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency|not_provided": 1,
    "not_provided|SLC16A1-related_disorder": 3,
    "not_provided|Monocarboxylate_transporter_1_deficiency|_autosomal_dominant|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency|Metabolic_myopathy_due_to_lactate_transporter_defect": 1,
    "not_provided|Metabolic_myopathy_due_to_lactate_transporter_defect": 1,
    "Monocarboxylate_transporter_1_deficiency|_autosomal_dominant|not_provided": 2,
    "Exercise-induced_hyperinsulinism|not_specified|not_provided": 1,
    "SLC16A1-related_disorder|not_provided": 5,
    "not_provided|SLC16A1-related_disorder|Hyperinsulinism|_Dominant": 1,
    "not_provided|Hyperinsulinism|_Dominant|not_specified": 1,
    "not_provided|Metabolic_myopathy_due_to_lactate_transporter_defect|Exercise-induced_hyperinsulinism|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency": 1,
    "not_provided|not_specified|SLC16A1-related_disorder|Hyperinsulinism|_Dominant": 1,
    "not_provided|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency|Metabolic_myopathy_due_to_lactate_transporter_defect|Exercise-induced_hyperinsulinism|SLC16A1-related_disorder": 1,
    "Exercise-induced_hyperinsulinism|Metabolic_myopathy_due_to_lactate_transporter_defect|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency": 1,
    "not_provided|Monocarboxylate_transporter_1_deficiency|_autosomal_recessive|Ketoacidosis_due_to_monocarboxylate_transporter-1_deficiency": 1,
    "Exercise-induced_hyperinsulinism|not_specified": 1,
    "not_specified|Hyperinsulinism|_Dominant": 1,
    "LRIG2-related_disorder": 9,
    "not_specified|not_provided|LRIG2-related_disorder": 1,
    "Urofacial_syndrome_2": 8,
    "not_specified|Urofacial_syndrome_2": 1,
    "not_provided|LRIG2-related_disorder": 3,
    "LRIG2-related_disorder|not_provided": 2,
    "not_provided|Urofacial_syndrome_2": 2,
    "LRIG2-related_disorder|not_specified|not_provided": 1,
    "Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 32,
    "PTPN22-related_disorder|not_specified|not_provided": 1,
    "Diabetes_mellitus_type_1": 3,
    "chronic_fatigue_syndrome_with_infection-triggered_onset|not_provided|Diabetes_mellitus|_insulin-dependent|_susceptibility_to": 1,
    "not_provided|PTPN22-related_disorder": 4,
    "PTPN22-related_disorder|not_provided": 1,
    "PTPN22-related_disorder": 3,
    "Systemic_lupus_erythematosus": 14,
    "Diabetes_mellitus|_insulin-dependent|_susceptibility_to": 1,
    "Hereditary_spastic_paraplegia_47": 190,
    "not_provided|Hereditary_spastic_paraplegia_47": 9,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_47": 19,
    "not_provided|Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_47|not_provided": 4,
    "Hereditary_spastic_paraplegia_47|not_provided|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_47|not_specified|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_47": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "Hereditary_spastic_paraplegia_47|not_specified": 2,
    "AP4B1-related_disorder": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_47|not_provided": 2,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_47": 1,
    "AP4B1-related_disorder|not_provided|Hereditary_spastic_paraplegia_47|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_47": 4,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_47": 5,
    "Hereditary_spastic_paraplegia_47|Hereditary_spastic_paraplegia": 3,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_47|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|Spastic_paraplegia": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "not_specified|Hereditary_spastic_paraplegia_47": 3,
    "Spastic_paraplegia|Abnormal_brain_morphology": 2,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Hereditary_spastic_paraplegia_47|Spastic_paraplegia": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_47|Abnormality_of_the_nervous_system|Spastic_paraplegia|Intellectual_disability": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_47": 2,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "AP4-related_intellectual_disability_and_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_47|not_specified|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_47|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 2,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_47|not_provided": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_47|AP4B1-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "AP4B1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "AP4B1-related_disorder|Intellectual_disability|Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_47|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_47": 1,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|not_provided|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_47|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_47|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_47": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "Hereditary_spastic_paraplegia_47|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_47|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_47": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_47": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_47": 1,
    "not_provided|Hereditary_spastic_paraplegia": 43,
    "Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome": 28,
    "Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita": 42,
    "not_specified|Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome": 4,
    "Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome|not_specified": 6,
    "Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita|Hereditary_spastic_paraplegia_47|not_specified|not_provided": 1,
    "DCLRE1B-related_disorder|Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome": 3,
    "not_specified|Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_C": 168,
    "DCLRE1B-related_disorder|Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_8": 3,
    "not_specified|DCLRE1B-related_disorder": 1,
    "Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita|not_specified": 3,
    "Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_8": 1,
    "Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome|DCLRE1B-related_disorder": 1,
    "not_provided|Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita": 1,
    "not_specified|Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita": 3,
    "DCLRE1B-related_disorder": 2,
    "DCLRE1B-related_disorder|not_provided|Autosomal_recessive_dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome": 1,
    "Developmental_dysplasia_of_the_hip": 2,
    "DEVELOPMENTAL_DYSPLASIA_OF_THE_HIP_4": 1,
    "Muscle_AMP_deaminase_deficiency": 347,
    "Muscle_AMP_deaminase_deficiency|Inborn_genetic_diseases": 23,
    "Inborn_genetic_diseases|Muscle_AMP_deaminase_deficiency": 22,
    "not_provided|Muscle_AMP_deaminase_deficiency": 15,
    "Inborn_genetic_diseases|not_provided|Muscle_AMP_deaminase_deficiency": 2,
    "AMPD1-related_disorder|not_specified|not_provided|Muscle_AMP_deaminase_deficiency": 4,
    "not_provided|Muscle_AMP_deaminase_deficiency|not_specified": 3,
    "not_specified|not_provided|Muscle_AMP_deaminase_deficiency": 6,
    "not_provided|not_specified|Muscle_AMP_deaminase_deficiency": 3,
    "Muscle_AMP_deaminase_deficiency|not_specified|not_provided": 1,
    "Muscle_AMP_deaminase_deficiency|not_provided|AMPD1-related_disorder": 1,
    "not_specified|Muscle_AMP_deaminase_deficiency|not_provided": 2,
    "Autism|Muscle_AMP_deaminase_deficiency": 3,
    "AMPD1-related_disorder|Muscle_AMP_deaminase_deficiency": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Muscle_AMP_deaminase_deficiency": 2,
    "Muscle_AMP_deaminase_deficiency|not_provided": 11,
    "Muscle_AMP_deaminase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Muscle_AMP_deaminase_deficiency|AMPD1-related_disorder": 2,
    "Muscle_AMP_deaminase_deficiency|Hypercholesterolemia|_autosomal_dominant|_type_B|AMPD1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Muscle_AMP_deaminase_deficiency|AMPD1-related_disorder": 1,
    "Muscle_AMP_deaminase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Muscle_AMP_deaminase_deficiency|not_provided": 1,
    "Muscle_AMP_deaminase_deficiency|not_specified": 1,
    "not_provided|Muscle_AMP_deaminase_deficiency|AMPD1-related_disorder|not_specified": 1,
    "not_specified|not_provided|Muscle_AMP_deaminase_deficiency|AMPD1-related_disorder": 1,
    "AMPD1-related_disorder|Muscle_AMP_deaminase_deficiency|not_provided": 1,
    "AMPD1-related_disorder|not_provided|Muscle_AMP_deaminase_deficiency": 1,
    "AMPD1-related_disorder": 1,
    "Noonan_syndrome_6": 60,
    "Noonan_syndrome": 243,
    "not_provided|Noonan_syndrome_6": 6,
    "Noonan_syndrome_6|not_provided": 4,
    "RASopathy": 3444,
    "Cardiovascular_phenotype|RASopathy": 377,
    "RASopathy|not_provided": 141,
    "Noonan_syndrome|not_provided|not_specified|NRAS-related_disorder|Noonan_syndrome_6|RASopathy": 1,
    "RASopathy|not_specified|not_provided": 13,
    "Neurodevelopmental_disorder|RASopathy": 1,
    "not_provided|RASopathy": 166,
    "not_provided|Noonan_syndrome|Noonan_syndrome_6": 1,
    "RASopathy|NRAS-related_disorder": 2,
    "not_specified|RASopathy|not_provided": 15,
    "Cardiovascular_phenotype|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "NRAS-related_disorder": 3,
    "See_cases|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|not_provided": 22,
    "Noonan_syndrome_6|Cardiovascular_phenotype": 1,
    "not_specified|RASopathy|Noonan_syndrome_6|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_6|not_provided|Cardiovascular_phenotype|RASopathy|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype": 432,
    "not_specified|not_provided|Noonan_syndrome_6": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype": 31,
    "RASopathy|not_provided|not_specified": 15,
    "not_specified|RASopathy": 86,
    "not_provided|not_specified|RASopathy|NRAS-related_disorder": 1,
    "RASopathy|not_specified": 126,
    "not_provided|Focal-onset_seizure": 1,
    "not_provided|RASopathy|NRAS-related_disorder": 1,
    "RASopathy|Noonan_syndrome_6|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|NRAS-related_disorder|not_specified|Noonan_syndrome_6|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|NRAS-related_disorder": 1,
    "not_provided|RASopathy|not_specified": 10,
    "Pyogenic_granuloma": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 4,
    "Colorectal_cancer|RASopathy": 1,
    "Vascular_malformation|Large_congenital_melanocytic_nevus|Neurocutaneous_melanocytosis|Colorectal_cancer|Linear_nevus_sebaceous_syndrome|not_provided|Epidermal_nevus|Non-small_cell_lung_carcinoma|Noonan_syndrome_6|Thyroid_cancer|_nonmedullary|_2": 1,
    "Vascular_Tumors_Including_Pyogenic_Granuloma|Large_congenital_melanocytic_nevus|Epidermal_nevus|Colorectal_cancer|Neurocutaneous_melanocytosis|not_provided|RASopathy|Ras_Inhibitor_response": 1,
    "Prostate_cancer|_hereditary|_1": 1117,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_6": 1,
    "NRAS-related_disorder|Cardiovascular_phenotype|not_provided|Noonan_syndrome_1|Noonan_syndrome_6|RASopathy": 1,
    "Anemia|Noonan_syndrome": 1,
    "Noonan_syndrome_6|Cardiovascular_phenotype|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome|Noonan_syndrome_1|not_provided|Colorectal_cancer|RASopathy": 1,
    "RASopathy|not_specified|NRAS-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "RASopathy|Noonan_syndrome|Noonan_syndrome_6|Noonan_syndrome_1": 1,
    "Noonan_syndrome_6|RASopathy|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|NRAS-related_disorder|not_specified|not_provided|RASopathy|Noonan_syndrome_6": 1,
    "Epidermal_nevus|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|RASopathy|not_provided": 28,
    "not_provided|RASopathy|Noonan_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|RASopathy": 3,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 5,
    "not_provided|Noonan_syndrome_6|Autoimmune_lymphoproliferative_syndrome_type_4|Acute_megakaryoblastic_leukemia_in_down_syndrome|RASopathy|Juvenile_myelomonocytic_leukemia": 1,
    "Large_congenital_melanocytic_nevus|not_provided|Linear_nevus_sebaceous_syndrome|Acute_myeloid_leukemia|Noonan_syndrome_6|Carcinoma_of_colon": 1,
    "NRAS-related_disorder|not_specified|Noonan_syndrome_6|Cardiovascular_phenotype|not_provided|RASopathy": 1,
    "not_provided|RASopathy|Noonan_syndrome|Colorectal_cancer": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Myelodysplastic_syndrome_progressed_to_acute_myeloid_leukemia|not_provided|RASopathy|Colorectal_cancer": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|NRAS-related_disorder|Large_congenital_melanocytic_nevus|Colorectal_cancer|not_provided|RASopathy|Epidermal_nevus|Autoimmune_lymphoproliferative_syndrome_type_4|Noonan_syndrome_6|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Chronic_myelogenous_leukemia|_BCR-ABL1_positive": 2,
    "Noonan_syndrome_6|Increased_nuchal_translucency|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Colorectal_cancer|Juvenile_myelomonocytic_leukemia|Noonan_syndrome|not_provided|RASopathy|Noonan_syndrome_6": 1,
    "Noonan_syndrome_6|Large_congenital_melanocytic_nevus|Autoimmune_lymphoproliferative_syndrome_type_4|Neurocutaneous_melanocytosis|Linear_nevus_sebaceous_syndrome|Epidermal_nevus|Thyroid_cancer|_nonmedullary|_2|Colorectal_cancer|RASopathy": 1,
    "Noonan_syndrome_6|not_specified|not_provided": 1,
    "not_provided|Noonan_syndrome": 22,
    "CSDE1-related_disorder": 17,
    "not_provided|CSDE1-related_disorder|Inborn_genetic_diseases": 1,
    "Complex_neurodevelopmental_disorder": 69,
    "CSDE1-associated_neurodevelopmental_disorder": 1,
    "CSDE1-associated_disorder": 2,
    "CSDE1-related_disorder|not_provided": 3,
    "not_provided|CSDE1-related_disorder": 1,
    "Inborn_genetic_diseases|CSDE1-related_disorder": 2,
    "Mycotic_Aneurysm|_Intracranial|not_provided": 2,
    "Isolated_thyroid-stimulating_hormone_deficiency": 8,
    "not_provided|Isolated_thyroid-stimulating_hormone_deficiency|not_specified|Congenital_hypothyroidism": 1,
    "not_provided|Isolated_thyroid-stimulating_hormone_deficiency": 4,
    "TSHB-related_disorder": 1,
    "TSHB-related_disorder|not_provided|Isolated_thyroid-stimulating_hormone_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Isolated_thyroid-stimulating_hormone_deficiency": 1,
    "not_provided|TSHB-related_disorder": 1,
    "Inborn_genetic_diseases|Isolated_thyroid-stimulating_hormone_deficiency": 1,
    "Isolated_thyroid-stimulating_hormone_deficiency|Pituitary_hypothyroidism|not_provided": 1,
    "TSHB-related_disorder|not_provided": 1,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 109,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|Peripheral_neuropathy": 1,
    "NGF-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 1,
    "not_specified|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 4,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|not_provided": 3,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 11,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|not_provided": 5,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|not_provided|not_specified|NGF-related_disorder": 1,
    "NGF-related_disorder|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 1,
    "not_provided|not_specified|NGF-related_disorder|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 2,
    "Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|NGF-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|NGF-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|NGF-related_disorder|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 1,
    "not_provided|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|not_specified": 1,
    "NGF-related_disorder|not_specified|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers": 1,
    "not_provided|Congenital_sensory_neuropathy_with_selective_loss_of_small_myelinated_fibers|NGF-related_disorder": 1,
    "Neural_tube_defect|Caudal_regression_sequence": 10,
    "Sacral_defect_with_anterior_meningocele|Neural_tube_defect|not_provided": 4,
    "not_provided|Neural_tube_defect|Sacral_defect_with_anterior_meningocele": 11,
    "Neural_tube_defect|Sacral_defect_with_anterior_meningocele": 104,
    "Caudal_regression_sequence|Neural_tube_defect": 3,
    "Keratoconus": 32,
    "VANGL1-related_disorder|Neural_tube_defect|Sacral_defect_with_anterior_meningocele": 1,
    "VANGL1-related_disorder": 2,
    "not_provided|Sacral_defect_with_anterior_meningocele|Neural_tube_defect": 6,
    "Neural_tube_defect": 28,
    "Neural_tube_defect|Sacral_defect_with_anterior_meningocele|VANGL1-related_disorder|not_provided": 1,
    "Sacral_defect_with_anterior_meningocele|Neural_tube_defect": 16,
    "Sacral_defect_with_anterior_meningocele|Neural_tube_defect|not_provided|not_specified": 1,
    "Sacral_defect_with_anterior_meningocele|Neural_tube_defects|_susceptibility_to|Neural_tube_defect": 1,
    "Neural_tube_defects|_susceptibility_to": 14,
    "Neural_tube_defect|Sacral_defect_with_anterior_meningocele|Inborn_genetic_diseases": 7,
    "Caudal_regression_sequence|not_provided": 1,
    "Neural_tube_defect|Sacral_defect_with_anterior_meningocele|not_provided": 6,
    "Sacral_defect_with_anterior_meningocele|not_provided": 1,
    "not_provided|Neural_tube_defects|_susceptibility_to": 1,
    "Sacral_defect_with_anterior_meningocele": 1,
    "Neural_tube_defect|not_provided|Sacral_defect_with_anterior_meningocele": 4,
    "Neural_tube_defects|_susceptibility_to|Sacral_defect_with_anterior_meningocele": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Neural_tube_defect|Sacral_defect_with_anterior_meningocele": 5,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Neural_tube_defect|not_provided|Sacral_defect_with_anterior_meningocele": 1,
    "Sacral_defect_with_anterior_meningocele|Neural_tube_defect|Caudal_regression_sequence": 1,
    "Neural_tube_defect|Caudal_regression_sequence|Sacral_defect_with_anterior_meningocele": 1,
    "not_provided|Neural_tube_defect|Sacral_defect_with_anterior_meningocele|Catecholaminergic_polymorphic_ventricular_tachycardia": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Neural_tube_defect|Sacral_defect_with_anterior_meningocele|not_provided": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Neural_tube_defect|Sacral_defect_with_anterior_meningocele": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Neural_tube_defect|Caudal_regression_sequence": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2": 32,
    "Catecholaminergic_polymorphic_ventricular_tachycardia": 809,
    "Neural_tube_defect|Caudal_regression_sequence|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Neural_tube_defect|Caudal_regression_sequence|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Neural_tube_defect|Caudal_regression_sequence|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 5,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 3,
    "Caudal_regression_sequence|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Neural_tube_defect|not_provided": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Neural_tube_defect|Caudal_regression_sequence|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3486,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 8,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Neural_tube_defect|Caudal_regression_sequence|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 241,
    "not_provided|not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Cardiovascular_phenotype|Progressive_familial_heart_block|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Caudal_regression_sequence|Neural_tube_defect|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 217,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 8,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 59,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 12,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 7,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 9,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype": 8,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Caudal_regression_sequence|Neural_tube_defect|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Cardiomyopathy|Caudal_regression_sequence|not_provided|Neural_tube_defect|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 86,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 7,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided": 6,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 4,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype|not_specified": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 93,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 3,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 2,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 20,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|CASQ2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 54,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|CASQ2-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype|not_provided": 3,
    "CASQ2-related_disorder|Sudden_unexplained_death|Cardiovascular_phenotype|Polymorphic_ventricular_tachycardia|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 1,
    "not_provided|CASQ2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|not_specified": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|CASQ2-related_disorder|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|CASQ2-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Conduction_disorder_of_the_heart|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 15,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_2": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 2,
    "Wolff-Parkinson-White_pattern|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_2|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 12,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 12,
    "Hypogonadotropic_hypogonadism_27_without_anosmia|Hypogonadotropic_hypogonadism": 1,
    "Hypogonadotropic_hypogonadism": 43,
    "Charcot-Marie-tooth_disease|_axonal|_type_2DD": 10,
    "Intellectual_disability|Charcot-Marie-tooth_disease|_axonal|_type_2DD|Hypomagnesemia|_seizures|_and_intellectual_disability_2|not_provided|not_specified": 1,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_2": 12,
    "ATP1A1-related_disorder|not_provided": 15,
    "Charcot-Marie-tooth_disease|_axonal|_type_2DD|Charcot-Marie-Tooth_disease_type_2A2|not_provided": 1,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_2|not_provided": 2,
    "not_provided|ATP1A1-related_disorder": 3,
    "Aldosterone-producing_adrenal_cortex_adenoma": 6,
    "ATP1A1-related_disorder": 5,
    "Inborn_genetic_diseases|ATP1A1-related_disorder": 1,
    "Charcot-Marie-tooth_disease|_axonal|_type_2DD|Hypomagnesemia|_seizures|_and_intellectual_disability_2": 1,
    "Charcot-Marie-tooth_disease|_axonal|_type_2DD|Hypomagnesemia|_seizures|_and_intellectual_disability_2|not_provided": 4,
    "not_provided|Charcot-Marie-tooth_disease|_axonal|_type_2DD|Hypomagnesemia|_seizures|_and_intellectual_disability_2": 2,
    "ATP1A1-related_disorder|not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_2|Charcot-Marie-tooth_disease|_axonal|_type_2DD": 1,
    "Marfanoid_habitus_and_intellectual_disability": 41,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_2|Charcot-Marie-tooth_disease|_axonal|_type_2DD|not_provided": 6,
    "ATP1A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Charcot-Marie-tooth_disease|_axonal|_type_2DD": 1,
    "Charcot-Marie-tooth_disease|_axonal|_type_2DD|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-tooth_disease|_axonal|_type_2DD": 2,
    "Charcot-Marie-tooth_disease|_axonal|_type_2DD|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "not_provided|Charcot-Marie-tooth_disease|_axonal|_type_2DD|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-tooth_disease|_axonal|_type_2DD": 1,
    "Intellectual_disability|Charcot-Marie-tooth_disease|_axonal|_type_2DD": 1,
    "not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_2": 1,
    "Calf_muscle_atrophy": 1,
    "not_specified|not_provided|ATP1A1-related_disorder": 1,
    "not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_2|Charcot-Marie-tooth_disease|_axonal|_type_2DD": 2,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_2|Charcot-Marie-tooth_disease|_axonal|_type_2DD|ATP1A1-related_disorder|not_provided": 1,
    "IGSF3-related_disorder": 7,
    "IGSF3-related_disorder|not_provided": 1,
    "not_specified|IGSF3-related_disorder": 1,
    "Familial_congenital_nasolacrimal_duct_obstruction": 2,
    "Esophageal_atresia|Pyloric_stenosis": 28,
    "not_provided|Familial_congenital_nasolacrimal_duct_obstruction": 1,
    "CD101-related_disorder": 2,
    "KBG_syndrome": 1219,
    "GDAP2-related_disorder": 6,
    "Spinocerebellar_ataxia|_autosomal_recessive_27": 7,
    "not_provided|GDAP2-related_disorder": 3,
    "SPAG17-related_disorder": 38,
    "SPAG17-related_disorder|not_specified|not_provided": 1,
    "SPAG17-related_disorder|not_provided": 4,
    "Spermatogenic_failure_55": 2,
    "not_provided|SPAG17-related_disorder": 1,
    "not_specified|Meniere_disease": 8,
    "Meniere_disease|Cranioectodermal_dysplasia_2": 1,
    "not_provided|Pelviscapular_dysplasia|Inborn_genetic_diseases": 1,
    "Pelviscapular_dysplasia|not_provided": 3,
    "not_specified|Pelviscapular_dysplasia|not_provided": 1,
    "Pelviscapular_dysplasia|not_provided|Inborn_genetic_diseases": 1,
    "TBX15-related_disorder": 6,
    "Inborn_genetic_diseases|Pelviscapular_dysplasia|not_provided": 1,
    "not_provided|TBX15-related_disorder": 1,
    "Pelviscapular_dysplasia": 2,
    "Pelviscapular_dysplasia|TBX15-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Pelviscapular_dysplasia": 4,
    "not_provided|Pelviscapular_dysplasia": 4,
    "not_provided|Pelviscapular_dysplasia|TBX15-related_disorder|not_specified": 1,
    "Pelviscapular_dysplasia|not_specified": 1,
    "Pelviscapular_dysplasia|not_provided|not_specified": 1,
    "TBX15-related_disorder|not_provided": 1,
    "WARS2-related_disorder": 4,
    "Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 6,
    "not_provided|Inborn_genetic_diseases|WARS2-related_disorder|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 1,
    "WARS2-related_disorder|not_provided": 4,
    "Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|not_provided": 4,
    "Parkinsonism-dystonia_3|_childhood-onset": 3,
    "Parkinsonism-dystonia_3|_childhood-onset|not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 1,
    "not_provided|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "WARS2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|WARS2-related_disorder|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 1,
    "Parkinsonism-dystonia_3|_childhood-onset|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 3,
    "not_provided|WARS2-related_disorder": 6,
    "Parkinsonism-dystonia_3|_childhood-onset|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|Parkinsonism-dystonia_3|_childhood-onset": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures": 1,
    "WARS2-related_disorder|Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|Neurodevelopmental_disorder|Parkinsonism-dystonia_3|_childhood-onset|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder|_mitochondrial|_with_abnormal_movements_and_lactic_acidosis|_with_or_without_seizures|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_adrenal_hyperplasia|not_provided": 4,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency": 77,
    "not_provided|HSD3B2-related_disorder": 2,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_provided": 18,
    "not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 28,
    "not_provided|Congenital_adrenal_hyperplasia|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 1,
    "not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency|HSD3B2-related_disorder": 2,
    "Inborn_genetic_diseases|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 5,
    "not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|Inborn_genetic_diseases": 3,
    "not_provided|Congenital_adrenal_hyperplasia": 5,
    "not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_specified": 1,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "HSD3B2-related_disorder|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 1,
    "Congenital_adrenal_hyperplasia": 28,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_provided|Congenital_adrenal_hyperplasia": 3,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|HSD3B2-related_disorder|not_provided": 1,
    "HSD3B2-related_disorder": 1,
    "HSD3B2-related_disorder|not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 1,
    "Hypospadias_1|_X-linked": 2,
    "not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency|HSD3B2-related_disorder|Congenital_adrenal_hyperplasia": 1,
    "HSD3B2-related_disorder|not_specified|3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_provided": 1,
    "not_specified|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 1,
    "Congenital_adrenal_hyperplasia|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 2,
    "HSD3B2-related_disorder|3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_provided|not_specified": 1,
    "Congenital_adrenal_hyperplasia|not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 1,
    "not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency|HSD3B2-related_disorder|not_specified": 1,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|Congenital_adrenal_hyperplasia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|3_beta-Hydroxysteroid_dehydrogenase_deficiency": 1,
    "HSD3B2-related_disorder|Congenital_adrenal_hyperplasia|3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_provided": 1,
    "3_beta-Hydroxysteroid_dehydrogenase_deficiency|not_specified|HSD3B2-related_disorder|not_provided": 1,
    "Androgen_deprivation_therapy_response": 1,
    "Androgen_deprivation_therapy_response|not_provided": 1,
    "PHGDH_deficiency": 692,
    "Neu-Laxova_syndrome_1|not_provided|PHGDH_deficiency": 3,
    "not_provided|Neu-Laxova_syndrome_1|PHGDH_deficiency": 4,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1": 13,
    "Inborn_genetic_diseases|PHGDH_deficiency": 13,
    "PHGDH_deficiency|not_provided|Neu-Laxova_syndrome_1": 4,
    "not_provided|PHGDH_deficiency": 11,
    "Neu-Laxova_syndrome_1|PHGDH_deficiency": 9,
    "Neu-Laxova_syndrome_1|Inborn_genetic_diseases|PHGDH_deficiency|not_provided": 1,
    "Neu-Laxova_syndrome_1|Inborn_genetic_diseases|PHGDH_deficiency": 3,
    "Neu-Laxova_syndrome_1|Inborn_genetic_diseases|not_provided|PHGDH_deficiency": 2,
    "not_provided|PHGDH_deficiency|Neu-Laxova_syndrome_1": 4,
    "Neu-Laxova_syndrome_1|PHGDH_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|PHGDH_deficiency": 3,
    "Neu-Laxova_syndrome_1|PHGDH_deficiency|not_provided": 5,
    "PHGDH_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|Seizure|Epileptic_encephalopathy|not_provided": 1,
    "not_specified|Neu-Laxova_syndrome_1|PHGDH_deficiency": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|not_provided": 5,
    "PHGDH_deficiency|not_provided": 6,
    "PHGDH_deficiency|Inborn_genetic_diseases": 4,
    "PHGDH-related_disorder|PHGDH_deficiency": 2,
    "PHGDH_deficiency|PHGDH-related_disorder": 6,
    "PHGDH_deficiency|Epileptic_encephalopathy|Seizure|Inborn_genetic_diseases": 1,
    "not_provided|PHGDH_deficiency|Inborn_genetic_diseases": 1,
    "PHGDH_deficiency|Inborn_genetic_diseases|Neu-Laxova_syndrome_1|not_provided": 2,
    "PHGDH-related_disorder|Neu-Laxova_syndrome_1|not_provided|PHGDH_deficiency": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|PHGDH-related_disorder|not_provided": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|not_provided|PHGDH-related_disorder|not_specified": 1,
    "Neu-Laxova_syndrome_1|PHGDH_deficiency|Inborn_genetic_diseases": 1,
    "Neu-Laxova_syndrome_1": 2,
    "PHGDH_deficiency|not_specified": 4,
    "not_specified|PHGDH_deficiency|Neu-Laxova_syndrome_1|not_provided": 1,
    "not_specified|Neu-Laxova_syndrome_1|not_provided|PHGDH_deficiency": 1,
    "PHGDH_deficiency|Inborn_genetic_diseases|Neu-Laxova_syndrome_1": 1,
    "Neu-Laxova_syndrome_1|not_provided|PHGDH_deficiency|Inborn_genetic_diseases": 1,
    "Neu-Laxova_syndrome_1|not_specified": 1,
    "PHGDH_deficiency|not_specified|Inborn_genetic_diseases|Neu-Laxova_syndrome_1": 1,
    "not_provided|PHGDH_deficiency|Neu-Laxova_syndrome_1|PHGDH-related_disorder": 1,
    "Inborn_genetic_diseases|PHGDH_deficiency|Neu-Laxova_syndrome_1": 1,
    "PHGDH_deficiency|not_specified|Neu-Laxova_syndrome_1": 1,
    "not_specified|not_provided|PHGDH_deficiency": 1,
    "Inborn_genetic_diseases|PHGDH_deficiency|Neu-Laxova_syndrome_1|not_provided": 1,
    "PHGDH_deficiency|not_provided|Inborn_genetic_diseases|Neu-Laxova_syndrome_1": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|not_specified": 1,
    "Neurometabolic_disorder_due_to_serine_deficiency|Neu-Laxova_syndrome_1|not_provided|PHGDH_deficiency": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|Inborn_genetic_diseases": 1,
    "PHGDH_deficiency|Neu-Laxova_syndrome_1|not_specified|not_provided": 1,
    "PHGDH-related_disorder|Neu-Laxova_syndrome_1|PHGDH_deficiency|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Neu-Laxova_syndrome_1|not_specified|PHGDH_deficiency|not_provided": 1,
    "PHGDH_deficiency|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|PHGDH_deficiency": 1,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|PHGDH_deficiency|not_provided": 1,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 177,
    "not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 11,
    "PHGDH_deficiency|not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "PHGDH_deficiency|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "HMGCS2-related_disorder|not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|not_specified": 6,
    "not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|Inborn_genetic_diseases": 1,
    "HMGCS2-related_disorder": 5,
    "not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|not_specified": 2,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|HMGCS2-related_disorder": 3,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 9,
    "not_specified|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "Inborn_genetic_diseases|HMGCS2-related_disorder|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|Inborn_genetic_diseases|HMGCS2-related_disorder": 1,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|not_provided": 7,
    "not_specified|not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 3,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|not_specified|HMGCS2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "not_specified|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|HMGCS2-related_disorder": 1,
    "not_specified|HMGCS2-related_disorder": 1,
    "HMGCS2-related_disorder|not_specified|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|3-hydroxy-3-methylglutaryl-CoA_synthase_deficiency": 1,
    "NOTCH2-related_disorder": 58,
    "Hajdu-Cheney_syndrome": 843,
    "not_provided|NOTCH2-related_disorder|Hajdu-Cheney_syndrome": 10,
    "Inborn_genetic_diseases|Hajdu-Cheney_syndrome": 24,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 8,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 129,
    "not_provided|Hajdu-Cheney_syndrome": 50,
    "Inborn_genetic_diseases|not_provided|Hajdu-Cheney_syndrome": 4,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Hajdu-Cheney_syndrome|not_specified": 5,
    "NOTCH2-related_disorder|Hajdu-Cheney_syndrome": 25,
    "Hajdu-Cheney_syndrome|not_provided": 42,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 50,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_1|See_cases": 1,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided": 12,
    "not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|NOTCH2-related_disorder": 1,
    "not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 8,
    "Hajdu-Cheney_syndrome|not_specified|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder": 27,
    "Hajdu-Cheney_syndrome|not_specified|NOTCH2-related_disorder": 2,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided|NOTCH2-related_disorder|not_specified": 1,
    "not_specified|not_provided|Hajdu-Cheney_syndrome": 12,
    "not_provided|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 9,
    "not_specified|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 2,
    "Hajdu-Cheney_syndrome|Inborn_genetic_diseases": 9,
    "NOTCH2-related_disorder|not_provided": 3,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 10,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_specified": 1,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder|not_provided": 3,
    "NOTCH2-related_disorder|Hajdu-Cheney_syndrome|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_specified": 1,
    "NOTCH2-related_disorder|Hajdu-Cheney_syndrome|not_provided": 2,
    "Hajdu-Cheney_syndrome|not_provided|NOTCH2-related_disorder": 3,
    "not_specified|Hajdu-Cheney_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 4,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|Inborn_genetic_diseases": 4,
    "Monoclonal_B-Cell_Lymphocytosis|Hajdu-Cheney_syndrome|not_provided": 1,
    "NOTCH2-related_disorder|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 3,
    "NOTCH2-related_disorder|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 3,
    "not_provided|Hajdu-Cheney_syndrome|Inborn_genetic_diseases": 5,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "NOTCH2-related_disorder|not_provided|Hajdu-Cheney_syndrome": 7,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|NOTCH2-related_disorder": 4,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 26,
    "Inborn_genetic_diseases|not_provided|Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_specified": 1,
    "NOTCH2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 2,
    "See_cases|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "Hajdu-Cheney_syndrome|not_provided|not_specified": 1,
    "NOTCH2-related_disorder|not_specified|not_provided|Hajdu-Cheney_syndrome": 3,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder": 3,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Inborn_genetic_diseases": 1,
    "NOTCH2-related_disorder|Inborn_genetic_diseases|not_provided|Hajdu-Cheney_syndrome": 2,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_specified|not_provided": 1,
    "See_cases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 1,
    "Hajdu-Cheney_syndrome|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder": 1,
    "Inborn_genetic_diseases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided": 3,
    "not_specified|NOTCH2-related_disorder": 1,
    "Hajdu-Cheney_syndrome|not_specified|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "Hajdu-Cheney_syndrome|Inborn_genetic_diseases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hajdu-Cheney_syndrome": 4,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 1,
    "Hajdu-Cheney_syndrome|not_specified": 4,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_specified": 3,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided|Hajdu-Cheney_syndrome": 1,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 3,
    "Hajdu-Cheney_syndrome|Inborn_genetic_diseases|NOTCH2-related_disorder": 3,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_specified": 1,
    "NOTCH2-related_disorder|Hajdu-Cheney_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_heart_anomalies": 1,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided|Hajdu-Cheney_syndrome": 1,
    "Hajdu-Cheney_syndrome|not_provided|not_specified|NOTCH2-related_disorder": 1,
    "Hajdu-Cheney_syndrome|Premature_ovarian_failure": 1,
    "not_provided|NOTCH2-related_disorder|Hajdu-Cheney_syndrome|not_specified": 1,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_specified|not_provided": 4,
    "NOTCH2-related_disorder|not_provided|Inborn_genetic_diseases|Hajdu-Cheney_syndrome": 1,
    "not_provided|Hajdu-Cheney_syndrome|NOTCH2-related_disorder": 7,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder|not_provided": 1,
    "NOTCH2-related_disorder|not_provided|not_specified|Hajdu-Cheney_syndrome": 1,
    "Hajdu-Cheney_syndrome|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Inborn_genetic_diseases": 1,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 1,
    "Inborn_genetic_diseases|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 3,
    "NOTCH2-related_disorder|not_specified|Hajdu-Cheney_syndrome": 1,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided|not_specified": 1,
    "not_provided|NOTCH2-related_disorder|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 2,
    "Inborn_genetic_diseases|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder|not_provided": 1,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Inborn_genetic_diseases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 1,
    "not_specified|Hajdu-Cheney_syndrome": 2,
    "NOTCH2-related_disorder|not_provided|Hajdu-Cheney_syndrome|not_specified": 1,
    "Hajdu-Cheney_syndrome|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 2,
    "Hajdu-Cheney_syndrome|not_provided|NOTCH2-related_disorder|Inborn_genetic_diseases": 1,
    "NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|Inborn_genetic_diseases": 2,
    "Hajdu-Cheney_syndrome|not_specified|NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "Hajdu-Cheney_syndrome|not_specified|not_provided": 5,
    "not_provided|NOTCH2-related_disorder": 3,
    "not_provided|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder": 1,
    "not_provided|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_specified": 1,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided|VATER_association": 1,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder|Hajdu-Cheney_syndrome": 1,
    "Hajdu-Cheney_syndrome|not_specified|not_provided|Inborn_genetic_diseases|NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|Inborn_genetic_diseases": 1,
    "Hajdu-Cheney_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|NOTCH2-related_disorder": 1,
    "not_specified|not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome": 1,
    "not_specified|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "NOTCH2-related_disorder|Inborn_genetic_diseases|Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 1,
    "not_specified|not_provided|Hajdu-Cheney_syndrome|NOTCH2-related_disorder|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract": 51,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_specified|not_provided": 1,
    "not_provided|Hajdu-Cheney_syndrome|not_specified|NOTCH2-related_disorder": 1,
    "Keratoacanthoma": 4,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Alagille_syndrome_due_to_a_NOTCH2_point_mutation|Hajdu-Cheney_syndrome|not_provided|NOTCH2-related_disorder": 2,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder|Inborn_genetic_diseases": 1,
    "NOTCH2-related_disorder|Inborn_genetic_diseases|Hajdu-Cheney_syndrome": 1,
    "Hajdu-Cheney_syndrome|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|NOTCH2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KA-like_vemurafenib-induced_squamous_lesions": 2,
    "not_provided|Alagille_syndrome_due_to_a_NOTCH2_point_mutation": 1,
    "not_specified|Alagille_syndrome_due_to_a_NOTCH2_point_mutation|not_provided": 1,
    "not_provided|Decreased_total_neutrophil_count|Decreased_total_lymphocyte_count": 7,
    "POLR3C-related_disorder": 10,
    "PEX11B-related_disorder": 4,
    "not_provided|Peroxisome_biogenesis_disorder_14B|Inborn_genetic_diseases": 1,
    "not_provided|Peroxisome_biogenesis_disorder_14B": 2,
    "PEX11B-related_disorder|not_provided": 4,
    "Peroxisome_biogenesis_disorder_14B": 8,
    "not_provided|PEX11B-related_disorder|Peroxisome_biogenesis_disorder_14B|Inborn_genetic_diseases": 1,
    "PEX11B-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_14B|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|PEX11B-related_disorder|not_provided": 1,
    "not_provided|PEX11B-related_disorder": 2,
    "PEX11B-related_disorder|not_provided|Peroxisome_biogenesis_disorder_14B": 1,
    "Peroxisome_biogenesis_disorder_14B|Radial_aplasia-thrombocytopenia_syndrome|not_provided": 1,
    "Peroxisome_biogenesis_disorder_14B|not_provided": 4,
    "PEX11B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|GPR89B-related_condition|Radial_aplasia-thrombocytopenia_syndrome": 1,
    "Radial_aplasia-thrombocytopenia_syndrome": 54,
    "RBM8A-related_disorder|not_provided|Radial_aplasia-thrombocytopenia_syndrome": 1,
    "not_provided|Radial_aplasia-thrombocytopenia_syndrome": 2,
    "Radial_aplasia-thrombocytopenia_syndrome|Inborn_genetic_diseases": 1,
    "Radial_aplasia-thrombocytopenia_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Radial_aplasia-thrombocytopenia_syndrome": 1,
    "Radial_aplasia-thrombocytopenia_syndrome|not_provided": 2,
    "Radial_aplasia-thrombocytopenia_syndrome|RBM8A-related_disorder": 1,
    "Abnormal_brain_morphology|Global_developmental_delay|Clinodactyly_of_the_5th_finger|RBM8A-related_disorder|Radial_aplasia-thrombocytopenia_syndrome|not_provided": 1,
    "RBM8A-related_disorder|Inborn_genetic_diseases|not_provided|Radial_aplasia-thrombocytopenia_syndrome": 1,
    "Short_stature|_oligodontia|_dysmorphic_facies|_and_motor_delay|POLR3GL-related_disorder|Oligodontia|Abnormal_facial_shape|Short_stature|Hyperostosis": 1,
    "Short_stature|_oligodontia|_dysmorphic_facies|_and_motor_delay|Oligodontia|Abnormal_facial_shape|Short_stature|Hyperostosis": 1,
    "POLR3GL-related_disorder|Short_stature|_oligodontia|_dysmorphic_facies|_and_motor_delay": 1,
    "Hemochromatosis_type_2A": 67,
    "Hemochromatosis_type_2A|not_provided": 24,
    "not_provided|Hemochromatosis_type_2A": 29,
    "not_specified|Hemochromatosis_type_2A": 1,
    "Hemochromatosis_type_2A|not_specified": 2,
    "Hemochromatosis_type_1|Hemochromatosis_type_2A": 1,
    "Juvenile_hemochromatosis|not_provided|Hemochromatosis_type_1|Hemochromatosis_type_2A": 1,
    "not_provided|Hemochromatosis_type_2A|Juvenile_hemochromatosis": 1,
    "not_specified|Hemochromatosis_type_2A|not_provided": 1,
    "not_provided|HJV-related_disorder": 3,
    "not_specified|HJV-related_disorder": 1,
    "Hemochromatosis_type_2A|not_provided|not_specified": 1,
    "HJV-related_disorder": 2,
    "HJV-related_disorder|not_provided|Hemochromatosis_type_2A": 2,
    "not_provided|Juvenile_hemochromatosis": 1,
    "not_specified|not_provided|Hemochromatosis_type_2A": 1,
    "Juvenile_hemochromatosis": 2,
    "not_provided|CHD1L-related_disorder": 3,
    "CHD1L-related_disorder": 15,
    "Abnormality_of_the_urinary_system": 1,
    "CHD1L-related_disorder|not_provided": 2,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 10,
    "not_specified|not_provided|CHD1L-related_disorder": 1,
    "CHD1L-related_disorder|not_specified": 1,
    "Short_stature|not_provided|CHD1L-related_disorder": 1,
    "Decreased_total_neutrophil_count|Decreased_total_lymphocyte_count": 7,
    "not_specified|CHD1L-related_disorder": 1,
    "BCL9-related_disorder": 3,
    "BCL9-related_disorder|not_specified|not_provided": 1,
    "not_specified|BCL9-related_disorder": 1,
    "Familial_atrial_fibrillation": 4,
    "Atrial_fibrillation|_familial|_11": 18,
    "not_provided|Familial_atrial_fibrillation": 3,
    "not_provided|Atrial_fibrillation|_familial|_11": 1,
    "Atrial_standstill_1|Atrial_fibrillation|_familial|_11": 103,
    "Atrial_fibrillation|_familial|_11|Atrial_standstill_1": 115,
    "Atrial_standstill_1|Atrial_fibrillation|_familial|_11|not_provided": 3,
    "Inborn_genetic_diseases|Atrial_fibrillation|_familial|_11|Atrial_standstill_1": 6,
    "Atrial_fibrillation|_familial|_11|Atrial_standstill_1|not_provided": 4,
    "Inborn_genetic_diseases|Atrial_fibrillation|_familial|_11|Atrial_standstill_1|Chromosome_1q21.1_deletion_syndrome": 1,
    "Inborn_genetic_diseases|Atrial_standstill_1|Atrial_fibrillation|_familial|_11": 2,
    "not_provided|Atrial_standstill_1|Atrial_fibrillation|_familial|_11": 8,
    "Atrial_standstill_1": 1,
    "Atrial_fibrillation|_familial|_11|Atrial_standstill_1|not_specified|not_provided": 1,
    "not_specified|Atrial_fibrillation|_familial|_11|Atrial_standstill_1|not_provided": 1,
    "not_provided|Atrial_fibrillation|_familial|_11|Atrial_standstill_1": 7,
    "Atrial_fibrillation|_familial|_11|Atrial_standstill_1|Inborn_genetic_diseases": 3,
    "not_provided|Familial_atrial_fibrillation|Atrial_fibrillation|_familial|_11|Atrial_standstill_1|not_specified": 1,
    "Inborn_genetic_diseases|Atrial_standstill_1|Atrial_fibrillation|_familial|_11|Chromosome_1q21.1_deletion_syndrome": 1,
    "Atrial_standstill_1|Atrial_fibrillation|_familial|_11|Inborn_genetic_diseases": 2,
    "Atrial_fibrillation|_familial|_11|Inborn_genetic_diseases": 1,
    "not_provided|Atrial_fibrillation|_familial|_11|Atrial_standstill_1|Atrial_fibrillation": 1,
    "Atrial_fibrillation|_somatic": 1,
    "GJA5-related_disorder|Atrial_fibrillation|_familial|_11|Atrial_standstill_1": 1,
    "Atrial_fibrillation|_familial|_11|not_provided": 1,
    "Atrial_fibrillation|_familial|_11|Atrial_standstill_1|Familial_atrial_fibrillation|not_provided": 1,
    "Familial_atrial_fibrillation|not_provided": 2,
    "Cataract_1_multiple_types": 137,
    "Cataract_1_multiple_types|Zonular_Pulverulent_Cataract": 9,
    "Zonular_Pulverulent_Cataract|Cataract_1_multiple_types": 1,
    "GJA8-related_disorder": 9,
    "Cataract_1_multiple_types|GJA8-related_disorder": 1,
    "Inborn_genetic_diseases|Cataract_1_multiple_types": 2,
    "Cataract_1_multiple_types|not_provided|Developmental_cataract": 2,
    "Developmental_cataract|Cataract_1_multiple_types": 3,
    "not_provided|Cataract_1_multiple_types": 5,
    "Cataract_1_multiple_types|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_cataract|GJA8-related_disorder|Cataract_1_multiple_types": 1,
    "Cataract_1_multiple_types|Inborn_genetic_diseases": 5,
    "Cataract_1_multiple_types|acorea|microphthalmia_and_cataract_syndrome": 1,
    "Cataract_1_multiple_types|acorea-microphthalmia-cataract_syndrome|Developmental_cataract": 1,
    "Microphthalmia_and_cataract|Cataract_1_multiple_types": 1,
    "Microphthalmia": 35,
    "Cataract_1_multiple_types|not_provided": 5,
    "Zonular_Pulverulent_Cataract|not_provided|Cataract_1_multiple_types": 3,
    "Cataract_1_multiple_types|Anterior_segment_dysgenesis": 1,
    "Cataract_1_multiple_types|not_provided|Anterior_segment_dysgenesis": 1,
    "GJA8-related_disorder|Cataract_1_multiple_types": 1,
    "Cataract_1_multiple_types|Developmental_cataract": 2,
    "GJA8-related_disorder|not_provided": 1,
    "GJA8-related_disorder|Cataract_1_multiple_types|Chromosome_1q21.1_deletion_syndrome|Zonular_Pulverulent_Cataract|not_provided|Developmental_cataract": 1,
    "GJA8-related_disorder|not_provided|Cataract_1_multiple_types": 1,
    "Zonular_Pulverulent_Cataract|not_provided|Cataract_1_multiple_types|not_specified": 1,
    "Cataract_1_multiple_types|Zonular_Pulverulent_Cataract|Inborn_genetic_diseases": 2,
    "Chromosome_1q21.1_deletion_syndrome": 1,
    "Cataract_1_multiple_types|GJA8-related_disorder|Inborn_genetic_diseases": 1,
    "Cataract_1_multiple_types|Zonular_Pulverulent_Cataract|not_provided": 1,
    "RNVU1-22-associated_neurodevelopmental_disorder|not_provided": 1,
    "RNVU1-27-associated_neurodevelopmental_disorder|not_provided": 1,
    "FCGR1A-related_disorder|not_provided|IGG_receptor_I|_phagocytic|_familial_deficiency_of": 1,
    "Peritoneal_Gliomatosis": 1,
    "Developmental_and_epileptic_encephalopathy_113": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_113": 1,
    "Developmental_and_epileptic_encephalopathy_113|See_cases": 1,
    "SV2A-related_disorder": 1,
    "Nager_syndrome": 26,
    "Nager_syndrome|not_provided": 2,
    "Nager_syndrome|Inborn_genetic_diseases": 2,
    "SF3B4-related_disorder": 10,
    "not_specified|Inborn_genetic_diseases|not_provided|Nager_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Nager_syndrome": 1,
    "Nager_syndrome|not_specified|not_provided": 1,
    "not_provided|Nager_syndrome": 4,
    "Inborn_genetic_diseases|SF3B4-related_disorder|not_provided": 1,
    "SF3B4-related_disorder|not_provided": 3,
    "SF3B4-related_acrofacial_dysostosis": 1,
    "Hereditary_hearing_loss_and_deafness|not_provided": 2,
    "Inborn_genetic_diseases|Nager_syndrome": 1,
    "not_provided|SF3B4-related_disorder": 2,
    "Metaphyseal_chondrodysplasia|_Schmid_type": 77,
    "Cleft_palate": 12,
    "VPS45-related_disorder|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_specified": 1,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 521,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|Inborn_genetic_diseases": 12,
    "VPS45-related_disorder|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 4,
    "Inborn_genetic_diseases|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 9,
    "not_provided|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 4,
    "not_specified|Inborn_genetic_diseases|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 1,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_provided|not_specified": 1,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_provided": 6,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_specified|not_provided": 1,
    "not_provided|VPS45-related_disorder|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_specified": 1,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_specified": 7,
    "not_provided|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|not_specified": 1,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "VPS45-related_disorder": 1,
    "Severe_congenital_neutropenia|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 1,
    "not_provided|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|VPS45-related_disorder": 1,
    "not_provided|not_specified|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 1,
    "not_specified|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 7,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|VPS45-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome": 1,
    "Congenital_neutropenia-myelofibrosis-nephromegaly_syndrome|VPS45-related_disorder|not_specified": 1,
    "APH1A-related_disorder": 1,
    "Retinitis_Pigmentosa|_Dominant": 30,
    "not_provided|Retinitis_Pigmentosa|_Dominant": 6,
    "Retinitis_pigmentosa_18": 6,
    "Retinitis_pigmentosa|not_provided|PRPF3-related_disorder": 3,
    "not_provided|Retinitis_pigmentosa_18": 1,
    "PRPF3-related_disorder|not_provided": 3,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_18": 1,
    "Retinitis_pigmentosa_18|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_18|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_18": 1,
    "Retinitis_pigmentosa_18|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|PRPF3-related_disorder": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_21|not_provided": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_21": 1,
    "not_specified|TARS2-related_disorder|not_provided": 1,
    "TARS2-related_disorder": 6,
    "Combined_oxidative_phosphorylation_defect_type_21|Inborn_genetic_diseases": 1,
    "not_provided|TARS2-related_disorder|not_specified": 1,
    "Combined_oxidative_phosphorylation_defect_type_21|not_provided": 6,
    "Neurodevelopmental_disorder|Combined_oxidative_phosphorylation_defect_type_21": 1,
    "Combined_oxidative_phosphorylation_defect_type_21": 17,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_21": 7,
    "Combined_oxidative_phosphorylation_defect_type_21|TARS2-related_disorder": 2,
    "not_provided|TARS2-related_disorder": 2,
    "Combined_oxidative_phosphorylation_defect_type_21|Failure_to_thrive|Spastic_hemiparesis|Congenital_blindness": 1,
    "Combined_oxidative_phosphorylation_defect_type_21|Neurodevelopmental_disorder": 1,
    "TARS2-related_disorder|not_provided|not_specified": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_21|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|TARS2-related_disorder": 1,
    "TARS2-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_21": 1,
    "Combined_oxidative_phosphorylation_defect_type_21|not_specified|not_provided": 1,
    "Lipid_proteinosis": 30,
    "Lipid_proteinosis|not_provided": 5,
    "ECM1-related_disorder": 6,
    "ECM1-related_disorder|not_provided": 1,
    "not_provided|Lipid_proteinosis": 3,
    "Lipid_proteinosis|ECM1-related_disorder|not_provided": 1,
    "ECM1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Lipid_proteinosis": 1,
    "Lipid_proteinosis|ECM1-related_disorder": 1,
    "Autism|Lipid_proteinosis": 1,
    "not_provided|ECM1-related_disorder": 3,
    "Lipid_proteinosis|not_provided|ECM1-related_disorder": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive": 29,
    "not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 8,
    "not_provided|ADAMTSL4-related_disorder": 7,
    "ADAMTSL4-related_disorder|not_provided": 10,
    "Inborn_genetic_diseases|not_provided|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 3,
    "Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 13,
    "ADAMTSL4-related_disorder|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 2,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae|Inborn_genetic_diseases|not_provided": 2,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|ADAMTSL4-related_disorder|not_provided": 2,
    "not_provided|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 10,
    "Inborn_genetic_diseases|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae|not_provided": 2,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 18,
    "not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae|not_specified": 1,
    "not_provided|ADAMTSL4-related_disorder|Ectopia_lentis_2|_isolated|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae": 2,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases|Ectopia_lentis_et_pupillae|not_provided": 5,
    "Inborn_genetic_diseases|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 1,
    "not_provided|Craniosynostosis_with_ectopia_lentis|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis|Inborn_genetic_diseases": 1,
    "Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 7,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Ectopia_lentis_et_pupillae": 6,
    "not_provided|Ectopia_lentis_et_pupillae|ADAMTSL4-related_disorder|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|not_specified|Ectopia_lentis_et_pupillae": 1,
    "Ectopia_lentis_et_pupillae|ADAMTSL4-related_disorder|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 2,
    "Ectopia_lentis_et_pupillae|Inborn_genetic_diseases|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 6,
    "not_provided|Ectopia_lentis_et_pupillae|Inborn_genetic_diseases|Ectopia_lentis_2|_isolated|_autosomal_recessive": 2,
    "Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 2,
    "ADAMTSL4-related_disorder": 6,
    "not_specified|Ectopia_lentis_et_pupillae|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae|not_provided": 4,
    "not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "ADAMTSL4-related_disorder|See_cases|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Ectopia_lentis_et_pupillae": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|ADAMTSL4-related_disorder|not_provided|Ectopia_lentis_et_pupillae": 3,
    "Ectopia_lentis_et_pupillae|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 7,
    "not_provided|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|ADAMTSL4-related_disorder|not_provided": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases|Ectopia_lentis_et_pupillae": 1,
    "Ectopia_lentis_et_pupillae|Inborn_genetic_diseases|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 5,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases|not_provided|Ectopia_lentis_et_pupillae": 6,
    "Ectopia_lentis_et_pupillae": 3,
    "not_provided|Craniosynostosis_syndrome|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "not_provided|Isolated_ectopia_lentis": 1,
    "Ectopia_lentis|not_provided": 2,
    "Isolated_ectopia_lentis": 1,
    "Inborn_genetic_diseases|Ectopia_lentis_et_pupillae|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 2,
    "not_provided|not_specified|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "Ectopia_lentis|ADAMTSL4-related_disorder|not_provided": 1,
    "not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases|Ectopia_lentis_et_pupillae": 3,
    "not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae": 4,
    "Ectopia_lentis_et_pupillae|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "ADAMTSL4-related_disorder|not_provided|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 2,
    "not_provided|Craniosynostosis_with_ectopia_lentis": 1,
    "Ectopia_lentis|not_provided|ADAMTSL4-related_disorder": 1,
    "Craniosynostosis_with_ectopia_lentis": 1,
    "not_provided|Ectopia_lentis_et_pupillae": 2,
    "Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Craniosynostosis_with_ectopia_lentis": 1,
    "ADAMTSL4-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Ectopia_lentis_et_pupillae": 1,
    "not_specified|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Ectopia_lentis_et_pupillae|not_specified": 1,
    "not_provided|Ectopia_lentis_et_pupillae|not_specified": 1,
    "Ectopia_lentis_et_pupillae|not_provided": 1,
    "ADAMTSL4-related_disorder|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 1,
    "not_provided|ADAMTSL4-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|ADAMTSL4-related_disorder|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "ADAMTSL4-related_disorder|not_provided|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "not_provided|not_specified|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae": 1,
    "ADAMTSL4-related_disorder|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Ectopia_lentis_et_pupillae": 1,
    "not_provided|Inborn_genetic_diseases|Ectopia_lentis_2|_isolated|_autosomal_recessive|Ectopia_lentis_et_pupillae": 1,
    "not_specified|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 2,
    "Ectopia_lentis": 2,
    "ADAMTSL4-related_disorder|Inborn_genetic_diseases|not_provided|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Ectopia_lentis_et_pupillae|Ectopia_lentis_2|_isolated|_autosomal_recessive|not_provided": 1,
    "Ectopia_lentis_2|_isolated|_autosomal_recessive|not_specified|not_provided|ADAMTSL4-related_disorder|Ectopia_lentis_et_pupillae": 1,
    "Pyknodysostosis": 105,
    "Pyknodysostosis|not_provided|Abnormality_of_the_skeletal_system": 1,
    "Pyknodysostosis|not_provided": 24,
    "not_provided|Pyknodysostosis": 29,
    "Midface_retrusion|Increased_susceptibility_to_fractures|Thoracic_scoliosis|Obtuse_angle_of_mandible|Enamel_hypoplasia|Short_finger|Nail_dysplasia|Delayed_closure_of_the_anterior_fontanelle|Periodontitis|Dental_crowding|Abnormal_skull_morphology|Abnormal_cranial_suture/fontanelle_morphology|Short_stature|Skeletal_dysplasia|Macrocephaly|Delayed_cranial_suture_closure|Short_phalanx_of_finger|Scoliosis|Pyknodysostosis|not_provided": 1,
    "CTSK-related_disorder|not_provided|Pyknodysostosis": 1,
    "Pyknodysostosis|not_provided|Inborn_genetic_diseases": 2,
    "Pyknodysostosis|not_specified|not_provided": 1,
    "not_specified|not_provided|Pyknodysostosis": 1,
    "Inborn_genetic_diseases|Pyknodysostosis|not_provided": 1,
    "Pyknodysostosis|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies": 14,
    "not_provided|PRUNE1-related_disorder": 5,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies|not_provided": 5,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies|Abnormal_brain_morphology|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies|not_provided|Abnormal_brain_morphology": 1,
    "PRUNE1-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies|Abnormal_brain_morphology": 1,
    "PRUNE1-related_disorder|not_provided": 4,
    "Abnormal_brain_morphology|Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies": 1,
    "PRUNE1-related_disorder|Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies": 1,
    "Orofaciodigital_syndrome_19": 2,
    "Intellectual_developmental_disorder_60_with_seizures": 13,
    "not_provided|ZNF687-related_disorder": 2,
    "ZNF687-related_disorder|not_provided": 4,
    "not_provided|not_specified|ZNF687-related_disorder": 1,
    "not_specified|Paget_disease_of_bone_6|not_provided": 1,
    "Paget_disease_of_bone_6": 2,
    "not_provided|not_specified|Paget_disease_of_bone_6": 1,
    "Paget_disease_of_bone_6|not_provided": 2,
    "not_provided|Paget_disease_of_bone_6": 2,
    "Paget_disease_of_bone_6|not_provided|not_specified": 1,
    "Paget_disease_of_bone_6|not_specified|not_provided": 1,
    "ZNF687-related_disorder": 1,
    "not_specified|PI4KB-related_disorder": 1,
    "Hearing_loss|_autosomal_dominant_87": 4,
    "PI4KB-related_disorder": 1,
    "MHC_class_II_deficiency": 2172,
    "not_provided|MHC_class_II_deficiency": 41,
    "MHC_class_II_deficiency|not_specified": 27,
    "not_specified|MHC_class_II_deficiency|RFX5-related_disorder": 1,
    "MHC_class_II_deficiency|MHC_class_II_deficiency_1": 1,
    "not_specified|MHC_class_II_deficiency": 41,
    "MHC_class_II_deficiency|not_specified|not_provided": 7,
    "RFX5-related_disorder": 3,
    "MHC_class_II_deficiency|not_provided": 46,
    "not_specified|not_provided|RFX5-related_disorder|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_3|not_provided": 1,
    "MHC_class_II_deficiency_1|MHC_class_II_deficiency|not_specified": 1,
    "MHC_class_II_deficiency_3": 4,
    "not_provided|not_specified|MHC_class_II_deficiency": 3,
    "RFX5-related_disorder|MHC_class_II_deficiency": 4,
    "not_specified|MHC_class_II_deficiency_3": 1,
    "not_specified|not_provided|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_3|MHC_class_II_deficiency_5|MHC_class_II_deficiency": 2,
    "MHC_class_II_deficiency|MHC_class_II_deficiency_3": 1,
    "MHC_class_II_deficiency|RFX5-related_disorder": 1,
    "not_provided|RFX5-related_disorder|not_specified|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_5|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_3|not_specified|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_5|MHC_class_II_deficiency_3": 1,
    "not_provided|MHC_class_II_deficiency_3": 1,
    "MHC_class_II_deficiency_1|not_provided|MHC_class_II_deficiency": 2,
    "SELENBP1-related_disorder": 10,
    "SELENBP1-related_disorder|not_provided": 1,
    "Extraoral_halitosis_due_to_methanethiol_oxidase_deficiency|Extra_oral_halitosis": 3,
    "Extraoral_halitosis_due_to_methanethiol_oxidase_deficiency": 2,
    "not_provided|SELENBP1-related_disorder": 1,
    "Proteasome-associated_autoinflammatory_syndrome_3|not_provided|PSMB4-related_disorder": 1,
    "PSMB4-related_disorder|not_provided": 3,
    "not_provided|Proteasome-associated_autoinflammatory_syndrome_3": 1,
    "PSMB4-related_disorder|Proteasome-associated_autoinflammatory_syndrome_3|not_specified|not_provided": 1,
    "Proteasome-associated_autoinflammatory_syndrome_3|not_specified|not_provided": 1,
    "not_provided|Proteasome-associated_autoinflammatory_syndrome_3|not_specified": 1,
    "Proteasome-associated_autoinflammatory_syndrome_3": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1": 33,
    "not_specified|PSMB4-related_disorder|Proteasome-associated_autoinflammatory_syndrome_3|not_provided": 1,
    "not_specified|not_provided|PSMB4-related_disorder": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|not_provided": 15,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 135,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 5,
    "Inborn_genetic_diseases|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|not_provided": 3,
    "not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 7,
    "POGZ-related_disorder|not_provided|Inborn_genetic_diseases|Autism_spectrum_disorder|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 1,
    "POGZ-related_disorder|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 1,
    "POGZ-related_disorder": 20,
    "not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Autism_spectrum_disorder": 1,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder": 1,
    "Autism_spectrum_disorder|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|POGZ-related_disorder": 3,
    "not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|See_cases": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Inborn_genetic_diseases|not_provided|POGZ-related_disorder": 2,
    "not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 10,
    "Autism_spectrum_disorder|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|Global_developmental_delay|Speech_apraxia|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|not_provided|POGZ-related_disorder": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|not_provided|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder": 1,
    "Inborn_genetic_diseases|Autism_spectrum_disorder": 6,
    "POGZ-related_disorder|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Inborn_genetic_diseases": 2,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Inborn_genetic_diseases": 5,
    "Hypertelorism|Microcephaly|Abnormal_nail_morphology|Downturned_corners_of_mouth|Generalized_hypotonia|Strabismus|Decreased_lacrimation|Brachycephaly|High_palate|Hypoplasia_of_the_corpus_callosum|Inability_to_walk_by_childhood/adolescence|Severe_global_developmental_delay|Sensorineural_hearing_loss_disorder|Absent_speech|Anteverted_nares|Wide_mouth|Seizure": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|not_provided|Inborn_genetic_diseases|POGZ-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 4,
    "Inborn_genetic_diseases|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|See_cases|not_provided": 1,
    "not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Smith-Magenis_Syndrome-like": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|POGZ-related_disorder": 3,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Intellectual_disability": 1,
    "not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|Autism_spectrum_disorder|POGZ-related_disorder": 1,
    "Autism_spectrum_disorder|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|not_provided": 1,
    "POGZ-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|intellectual_deficiency|dysmorphy|POGZ-related_disorder|See_cases": 1,
    "Autism_spectrum_disorder|POGZ-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 1,
    "Autism_spectrum_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Neurodevelopmental_disorder|not_provided|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome": 1,
    "Truncal_obesity|Hearing_impairment|Short_metacarpal|Intellectual_disability|Myopia|Hypothyroidism|Short_stature": 1,
    "not_provided|Inborn_genetic_diseases|POGZ-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder": 1,
    "Intellectual_disability-microcephaly-strabismus-behavioral_abnormalities_syndrome|POGZ-related_disorder": 1,
    "not_provided|not_specified|Autism_spectrum_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided": 10,
    "Nonsyndromic_Deafness": 2,
    "Woolly_hair-skin_fragility_syndrome": 2,
    "Severe_myoclonic_epilepsy_in_infancy": 758,
    "Severe_myoclonic_epilepsy_in_infancy|Inborn_genetic_diseases": 13,
    "Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy": 14,
    "Inborn_genetic_diseases|not_provided|Severe_myoclonic_epilepsy_in_infancy": 2,
    "not_provided|Severe_myoclonic_epilepsy_in_infancy": 35,
    "Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy|not_provided": 1,
    "SNX27-related_disorder|Severe_myoclonic_epilepsy_in_infancy": 4,
    "SNX27-related_disorder": 5,
    "Severe_myoclonic_epilepsy_in_infancy|not_provided": 9,
    "not_provided|SNX27-related_disorder|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|SNX27-related_disorder|not_provided": 1,
    "Severe_myoclonic_epilepsy_in_infancy|SNX27-related_disorder": 1,
    "Distal_spinal_muscular_atrophy|not_provided": 2,
    "Polymicrogyria": 3,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency": 234,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|RORC-related_disorder": 2,
    "not_specified|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency": 13,
    "not_provided|RORC-related_disorder|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|not_specified": 1,
    "RORC-related_disorder|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency": 6,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|not_provided": 4,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|Inborn_genetic_diseases": 8,
    "not_provided|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency": 3,
    "RORC-related_disorder|Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|not_provided": 1,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|not_specified|not_provided": 2,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_RORgamma_receptor_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Uncombable_hair_syndrome_3": 5,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "not_provided|FLG-related_disorder": 4,
    "Dermatitis|_atopic|_2|Ichthyosis_vulgaris|not_provided": 5,
    "Dermatitis|_atopic|_2": 10,
    "Ichthyosis_vulgaris": 73,
    "Ichthyosis_vulgaris|not_provided": 30,
    "Dermatitis|_atopic|_2|Ichthyosis_vulgaris": 6,
    "Ichthyosis_vulgaris|not_specified|not_provided|Dermatitis|_atopic|_2": 1,
    "Autosomal_dominant_ichthyosis_vulgaris|Ichthyosis_vulgaris|not_provided": 1,
    "not_provided|Ichthyosis_vulgaris": 44,
    "Autosomal_dominant_ichthyosis_vulgaris|Inborn_genetic_diseases": 1,
    "Ichthyosis_vulgaris|Dermatitis|_atopic|_2": 3,
    "not_provided|Ichthyosis_vulgaris|Autosomal_recessive_congenital_ichthyosis": 1,
    "not_provided|Dermatitis|_atopic|_2|Ichthyosis_vulgaris": 2,
    "Ichthyosis_vulgaris|Inborn_genetic_diseases": 8,
    "Palmoplantar_blistering|Palmoplantar_hyperhidrosis|Atrophic_scars|Ichthyosis|Ichthyosis_vulgaris": 1,
    "not_provided|Dermatitis|_atopic|_2": 1,
    "Autosomal_dominant_ichthyosis_vulgaris": 5,
    "Ichthyosis_vulgaris|not_provided|Dermatitis|_atopic|_2": 3,
    "not_provided|Inborn_genetic_diseases|FLG-related_disorder": 1,
    "FLG-related_disorder|Dermatitis|_atopic|_2|Ichthyosis_vulgaris|not_provided|See_cases": 1,
    "Ichthyosis_vulgaris|not_provided|not_specified": 2,
    "not_provided|Ichthyosis_vulgaris|not_specified": 1,
    "Ichthyosis_vulgaris|Inborn_genetic_diseases|not_provided": 1,
    "FLG-related_disorder": 14,
    "Ichthyosis_vulgaris|Dermatitis|_atopic|_2|not_provided": 5,
    "not_provided|Ichthyosis_vulgaris|Dermatitis|_atopic|_2": 4,
    "Inborn_genetic_diseases|Dermatitis|_atopic|_2|Ichthyosis_vulgaris": 3,
    "Ichthyosis_vulgaris|Dermatitis|_atopic|_2|not_provided|Dermatitis|_atopic|_2|_susceptibility_to": 1,
    "Ichthyosis_vulgaris|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Ichthyosis_vulgaris": 3,
    "Dermatitis|_atopic|_2|not_provided|FLG-related_disorder": 1,
    "FLG-related_disorder|Dermatitis|_atopic|Dermatitis|_atopic|_2|Ichthyosis_vulgaris|not_provided": 1,
    "Inborn_genetic_diseases|Ichthyosis_vulgaris|not_provided|Dermatitis|_atopic|_2": 1,
    "Inborn_genetic_diseases|Ichthyosis_vulgaris|not_provided": 2,
    "not_provided|not_specified|Ichthyosis_vulgaris": 2,
    "not_specified|not_provided|Ichthyosis_vulgaris": 1,
    "Ichthyosis_vulgaris|not_specified": 1,
    "not_provided|Ichthyosis_vulgaris|Incidental_Discovery": 1,
    "Dermatitis|_atopic|_2|Ichthyosis_vulgaris|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_ichthyosis_vulgaris|Dermatitis|_atopic|_2|_susceptibility_to|Ichthyosis_vulgaris|Dermatitis|_atopic|_2|not_provided": 1,
    "Autosomal_dominant_ichthyosis_vulgaris|not_provided|Ichthyosis_vulgaris": 1,
    "not_specified|Ichthyosis_vulgaris|not_provided": 3,
    "not_specified|FLG-related_disorder|not_provided": 1,
    "FLG-related_disorder|not_provided|Ichthyosis_vulgaris": 1,
    "FLG-related_disorder|not_provided": 12,
    "Inborn_genetic_diseases|FLG-related_disorder": 1,
    "FLG-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Ichthyosis_vulgaris|Dermatitis|_atopic|_2|FLG-related_disorder": 1,
    "not_provided|FLG-related_disorder|Ichthyosis_vulgaris|Dermatitis|_atopic|_2": 1,
    "Palmoplantar_keratodermas|Ichthyosis_and_erythrokeratoderma|Autosomal_recessive_congenital_ichthyosis|FLG-related_disorder|Autosomal_dominant_ichthyosis_vulgaris|Inborn_genetic_diseases|Dermatitis|_atopic|_2|Ichthyosis_vulgaris|not_provided|Dermatitis|_atopic|_2|_susceptibility_to|Eczematoid_dermatitis": 1,
    "not_specified|Dermatitis|_atopic|_2|Ichthyosis_vulgaris|not_provided": 1,
    "Ichthyosis_vulgaris|Atopic_eczema|FLG-related_disorder|Inborn_genetic_diseases|Dermatitis|_atopic|_2|not_provided|Dermatitis|_atopic|_2|_susceptibility_to|Eczematoid_dermatitis": 1,
    "not_provided|FLG-related_disorder|not_specified": 1,
    "FLG-related_disorder|not_specified|not_provided": 1,
    "Microcephaly|Congenital_cerebellar_hypoplasia|Paroxysmal_dystonia|Feeding_difficulties|Abnormality_of_salivation|Ichthyosis|Abnormality_of_the_skin|Dry_skin": 1,
    "not_provided|Autosomal_dominant_ichthyosis_vulgaris|Dermatitis|_atopic|_2|Ichthyosis_vulgaris": 1,
    "Ichthyosis_vulgaris|FLG-related_disorder|not_provided": 1,
    "Peeling_skin_syndrome_6": 3,
    "not_provided|Peeling_skin_syndrome_6": 3,
    "Peeling_skin_syndrome_6|not_provided": 1,
    "not_specified|Peeling_skin_syndrome_6": 1,
    "FLG2-related_disorder": 1,
    "Prostate_cancer|not_specified": 7,
    "Loricrin_keratoderma": 6,
    "Loricrin_keratoderma|not_provided": 1,
    "not_provided|Loricrin_keratoderma": 2,
    "PGLYRP3-associated_inflamatory_bowel_disease": 1,
    "Abnormal_brain_morphology|See_cases": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 52,
    "Inborn_genetic_diseases|not_specified|not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided": 19,
    "GATAD2B-related_intellectual_disability_syndrome": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|Inborn_genetic_diseases": 2,
    "GATAD2B-related_disorder|not_provided": 2,
    "not_specified|not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 3,
    "not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 12,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided|GATAD2B-related_disorder": 2,
    "not_specified|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided": 1,
    "not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|See_cases": 1,
    "not_provided|GATAD2B-related_disorder": 2,
    "not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|GATAD2B-related_disorder|not_specified": 1,
    "not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|Inborn_genetic_diseases": 3,
    "not_specified|Inborn_genetic_diseases|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided": 1,
    "GATAD2B-related_disorder|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|Intellectual_disability|not_provided": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|not_provided|GATAD2B-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "GATAD2B-related_disorder|GATAD2B-related_intellectual_disability_syndrome|not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome": 1,
    "not_provided|Severe_intellectual_disability-poor_language-strabismus-grimacing_face-long_fingers_syndrome|GATAD2B-related_disorder": 1,
    "GATAD2B-Related_Neurodevelopmental_Disorder": 1,
    "GATAD2B-related_disorder": 1,
    "DENND4B-related_disorder": 29,
    "Short_stature|DENND4B-related_disorder": 1,
    "not_specified|DENND4B-related_disorder": 3,
    "DENND4B-related_disorder|not_provided": 1,
    "not_provided|DENND4B-related_disorder": 1,
    "RPS27-related_disorder": 2,
    "not_provided|RPS27-related_disorder": 2,
    "Diamond-Blackfan_anemia_17": 2,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_4A|_autosomal_dominant": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 148,
    "Congenital_myopathy_with_fiber_type_disproportion|Nemaline_myopathy": 15,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 105,
    "Nemaline_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 8,
    "Congenital_myopathy_with_fiber_type_disproportion|not_provided|Nemaline_myopathy": 1,
    "Congenital_myopathy_4B|_autosomal_recessive|not_provided|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_4B|_autosomal_recessive|not_provided": 1,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 5,
    "Congenital_myopathy_4B|_autosomal_recessive": 10,
    "not_provided|Inborn_genetic_diseases|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_4A|_autosomal_dominant|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive|not_provided": 4,
    "not_specified|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive|not_provided": 1,
    "not_specified|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 1,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion": 6,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4A|_autosomal_dominant": 2,
    "not_specified|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 2,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 3,
    "not_specified|not_provided|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "TPM3-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_provided|not_specified": 1,
    "not_provided|TPM3-related_myopathy|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_with_fiber_type_disproportion": 22,
    "Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Congenital_myopathy_4A|_autosomal_dominant|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy|Congenital_myopathy_4A|_autosomal_dominant|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive|not_provided": 1,
    "TPM3-related_core_myopathy|Congenital_myopathy_4B|_autosomal_recessive|not_provided|Congenital_myopathy_4A|_autosomal_dominant|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "TPM3-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 1,
    "not_provided|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Centronuclear_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 1,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_specified": 1,
    "TPM3-related_disorder|not_specified|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive": 1,
    "Congenital_myopathy_4A|_autosomal_dominant|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_provided|not_specified|Nemaline_myopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_4A|_autosomal_dominant|not_provided": 1,
    "not_provided|Congenital_myopathy_4B|_autosomal_recessive|TPM3-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|not_specified": 1,
    "Inborn_genetic_diseases|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_4B|_autosomal_recessive|not_provided": 1,
    "not_provided|Congenital_myopathy_4B|_autosomal_recessive|Congenital_myopathy_4A|_autosomal_dominant": 1,
    "Neurodevelopmental_disorder_with_impaired_language|_behavioral_abnormalities|_and_dysmorphic_facies": 6,
    "UBAP2L-related_condition": 1,
    "not_provided|Neurodevelopmental_disorder_with_impaired_language|_behavioral_abnormalities|_and_dysmorphic_facies": 2,
    "Neurodevelopmental_disorder_with_impaired_language|_behavioral_abnormalities|_and_dysmorphic_facies|Global_developmental_delay": 1,
    "not_specified|Neurodevelopmental_disorder": 3,
    "Neurodevelopmental_disorder_with_impaired_language|_behavioral_abnormalities|_and_dysmorphic_facies|not_specified": 1,
    "Kostmann_syndrome": 261,
    "not_provided|Kostmann_syndrome": 9,
    "Inborn_genetic_diseases|not_provided|Kostmann_syndrome": 2,
    "Inborn_genetic_diseases|Kostmann_syndrome": 49,
    "Kostmann_syndrome|not_provided": 4,
    "Kostmann_syndrome|Inborn_genetic_diseases": 50,
    "Inborn_genetic_diseases|HAX1-related_disorder|not_provided|Kostmann_syndrome": 1,
    "Kostmann_syndrome|not_specified": 8,
    "not_provided|Kostmann_syndrome|not_specified": 1,
    "HAX1-related_disorder": 1,
    "Kostmann_syndrome|Severe_congenital_neutropenia|not_provided": 1,
    "HAX1-related_disorder|Kostmann_syndrome": 3,
    "Inborn_genetic_diseases|Kostmann_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Kostmann_syndrome|not_specified": 2,
    "not_provided|Kostmann_syndrome|Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified": 1,
    "Kostmann_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Kostmann_syndrome|Decreased_total_neutrophil_count": 1,
    "Kostmann_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|HAX1-related_disorder|not_specified|not_provided|Kostmann_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Kostmann_syndrome": 3,
    "Kostmann_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "HAX1-related_disorder|not_provided|Kostmann_syndrome": 1,
    "not_specified|Kostmann_syndrome": 2,
    "Kostmann_syndrome|HAX1-related_disorder": 2,
    "Kostmann_syndrome|not_provided|not_specified": 1,
    "Severe_congenital_neutropenia|Kostmann_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Kostmann_syndrome": 2,
    "not_provided|IL6R-related_disorder": 7,
    "IL6R-related_disorder|not_provided": 8,
    "Hyper-IgE_recurrent_infection_syndrome_5|_autosomal_recessive|not_specified|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_5|_autosomal_recessive": 4,
    "IL6R-related_disorder": 2,
    "Hyper-IgE_recurrent_infection_syndrome_5|_autosomal_recessive|not_provided": 2,
    "not_specified|IL6R-related_disorder": 1,
    "Interleukin_6|_serum_level_of|_quantitative_trait_locus|IL6R-related_disorder|Soluble_interleukin-6_receptor|_serum_level_of|_quantitative_trait_locus|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 109,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1165,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 41,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 138,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 6,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 15,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 42,
    "CHRNB2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 3,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 12,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 4,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 66,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 11,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|not_specified": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Inborn_genetic_diseases": 15,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 5,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Microcephaly|Seizure|Deeply_set_eye": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "Focal_clonic_seizure": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 36,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "CHRNB2-related_disorder": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|See_cases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 12,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 22,
    "CHRNB2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 7,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "CHRNB2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_provided": 11,
    "Inborn_genetic_diseases|CHRNB2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|CHRNB2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 6,
    "not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 2,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Generalized-onset_seizure": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|not_provided|Inborn_genetic_diseases|not_specified|CHRNB2-related_disorder": 1,
    "CHRNB2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_3|not_provided": 1,
    "Symmetrical_dyschromatosis_of_extremities": 85,
    "not_provided|Symmetrical_dyschromatosis_of_extremities": 3,
    "Symmetrical_dyschromatosis_of_extremities|not_provided": 6,
    "ADAR-related_disorder": 4,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities": 315,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 805,
    "not_provided|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 9,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_provided": 18,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|not_provided": 28,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|not_specified": 3,
    "Inborn_genetic_diseases|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|not_provided": 2,
    "Inborn_genetic_diseases|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 16,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_provided|not_specified": 1,
    "not_provided|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities": 5,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_specified": 1,
    "Aicardi-Goutieres_syndrome_6": 20,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|ADAR-related_disorder": 6,
    "Aicardi-Goutieres_syndrome_6|not_provided|Symmetrical_dyschromatosis_of_extremities": 5,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_provided": 2,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|not_provided|Inborn_genetic_diseases": 1,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|Inborn_genetic_diseases": 9,
    "ADAR-related_disorder|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 6,
    "ADAR-related_disorder|not_provided|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities": 2,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities": 14,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 1,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases": 17,
    "not_specified|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 3,
    "not_provided|Aicardi-Goutieres_syndrome_6|not_specified|Symmetrical_dyschromatosis_of_extremities": 1,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|ADAR-related_disorder|not_provided": 1,
    "Cerebral_calcification|Aicardi-Goutieres_syndrome_6|not_provided": 1,
    "not_specified|ADAR-related_disorder|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|not_provided": 1,
    "not_specified|not_provided|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities": 1,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|ADAR-related_disorder|not_specified": 1,
    "ADAR-related_type_1_interferonopathy|not_provided|Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases|Symmetrical_dyschromatosis_of_extremities": 1,
    "Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases|Symmetrical_dyschromatosis_of_extremities": 3,
    "not_provided|Aicardi-Goutieres_syndrome_6|ADAR-related_disorder|Symmetrical_dyschromatosis_of_extremities": 1,
    "Symmetrical_dyschromatosis_of_extremities|Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_6": 2,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|ADAR-related_disorder|not_provided": 1,
    "ADAR-related_disorder|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_provided": 1,
    "not_provided|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases": 1,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_provided": 1,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases|not_provided": 1,
    "Symmetrical_dyschromatosis_of_extremities|not_provided|Aicardi-Goutieres_syndrome_6": 1,
    "ADAR-related_disorder|Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases|not_provided|Symmetrical_dyschromatosis_of_extremities": 1,
    "Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|Intellectual_disability|not_provided": 1,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|ADAR-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6": 1,
    "Symmetrical_dyschromatosis_of_extremities|not_provided|Aicardi-Goutieres_syndrome_6|not_specified": 1,
    "ADAR-related_disorder|not_provided|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|Inborn_genetic_diseases": 1,
    "ADAR-related_disorder|Symmetrical_dyschromatosis_of_extremities|not_provided|Aicardi-Goutieres_syndrome_6": 1,
    "Inborn_genetic_diseases|ADAR-related_disorder|ADAR-related_type_1_interferonopathy|Symmetrical_dyschromatosis_of_extremities|Aicardi-Goutieres_syndrome_6|Aicardi_Goutieres_syndrome|not_provided": 1,
    "Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Symmetrical_dyschromatosis_of_extremities|not_provided|Aicardi-Goutieres_syndrome_6": 1,
    "ADAR-related_disorder|Aicardi-Goutieres_syndrome_6|not_provided|Symmetrical_dyschromatosis_of_extremities": 1,
    "not_provided|Aicardi-Goutieres_syndrome_6|Symmetrical_dyschromatosis_of_extremities|not_specified": 1,
    "Symmetrical_dyschromatosis_of_extremities|not_provided|not_specified|Aicardi-Goutieres_syndrome_6": 1,
    "Inborn_genetic_diseases|not_specified|Zimmermann-Laband_syndrome_3": 1,
    "Zimmermann-Laband_syndrome_3": 19,
    "KCNN3-related_disorder": 1,
    "not_specified|not_provided|Zimmermann-Laband_syndrome_3": 2,
    "not_provided|Pyloric_stenosis|Esophageal_atresia|not_specified|KCNN3-related_disorder": 1,
    "Zimmermann-Laband_syndrome_3|not_provided|not_specified": 1,
    "not_provided|not_specified|Zimmermann-Laband_syndrome_3": 1,
    "not_specified|KCNN3-related_disorder": 2,
    "Zimmermann-Laband_syndrome_3|not_specified": 1,
    "Porokeratosis_1|_Mibelli_type": 4,
    "PMVK-associated_autoinflammatory_disorder": 1,
    "Inborn_genetic_diseases|Porokeratosis_1|_Mibelli_type": 1,
    "Linear_porokeratosis": 3,
    "not_provided|PMVK-related_disorder": 1,
    "PMVK-related_disorder|not_provided": 1,
    "not_provided|PMVK-related_disorder|Linear_porokeratosis|Porokeratosis_1|_Mibelli_type": 1,
    "PMVK-related_disorder": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency": 1325,
    "Myopathy_with_abnormal_lipid_metabolism|not_provided": 4,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Myopathy_with_abnormal_lipid_metabolism": 2,
    "not_provided|Myopathy_with_abnormal_lipid_metabolism": 1,
    "Myopathy_with_abnormal_lipid_metabolism": 3,
    "Myopathy_with_abnormal_lipid_metabolism|Multiple_acyl-CoA_dehydrogenase_deficiency": 3,
    "FLAD1-related_disorder|not_provided": 6,
    "not_provided|FLAD1-related_disorder": 2,
    "FLAD1-related_disorder": 1,
    "not_provided|Myopathy_with_abnormal_lipid_metabolism|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Myopathy_with_abnormal_lipid_metabolism|Inborn_genetic_diseases|not_provided": 1,
    "FLAD1-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency|Myopathy_with_abnormal_lipid_metabolism|not_provided": 1,
    "DPM3-congenital_disorder_of_glycosylation|not_provided": 4,
    "DPM3-congenital_disorder_of_glycosylation": 36,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_impaired_intellectual_development)|_type_B|_15|DPM3-congenital_disorder_of_glycosylation": 2,
    "not_provided|DPM3-congenital_disorder_of_glycosylation|DPM3-related_disorder": 1,
    "DPM3-congenital_disorder_of_glycosylation|not_specified": 1,
    "not_provided|DPM3-congenital_disorder_of_glycosylation": 4,
    "not_specified|not_provided|DPM3-congenital_disorder_of_glycosylation": 1,
    "Myopathy|EMG:_myopathic_abnormalities|Cardiomyopathy": 1,
    "not_provided|not_specified|DPM3-congenital_disorder_of_glycosylation": 1,
    "MUC1-related_disorder": 7,
    "Tubulointerstitial_kidney_disease|_autosomal_dominant|_2": 16,
    "MUC1-related_disorder|Inborn_genetic_diseases": 1,
    "MUC1-related_disorder|Inborn_genetic_diseases|Kidney_failure|not_provided": 1,
    "not_provided|Tubulointerstitial_kidney_disease|_autosomal_dominant|_2|Inborn_genetic_diseases": 1,
    "Tubulointerstitial_kidney_disease|_autosomal_dominant|_2|Inborn_genetic_diseases": 1,
    "Tubulointerstitial_kidney_disease|_autosomal_dominant|_2|not_provided": 1,
    "Gaucher_disease_type_I": 42,
    "Lewy_body_dementia|Gaucher_disease_type_III|Gaucher_disease_type_II|Parkinson_disease|_late-onset|Gaucher_disease_type_I|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_perinatal_lethal": 1,
    "Gaucher_disease": 133,
    "Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_specified|not_provided|Gaucher_disease": 2,
    "not_provided|Gaucher_disease_type_II|Gaucher_disease_type_I|Gaucher_disease|Parkinson_disease|_late-onset": 1,
    "Gaucher_disease|Gaucher_disease_type_I": 3,
    "not_provided|not_specified|Gaucher_disease_type_I": 1,
    "Gaucher_disease_perinatal_lethal": 6,
    "Parkinson_disease|_late-onset|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided": 1,
    "Gaucher_disease|Gaucher_disease_type_I|not_provided|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Gaucher_disease_type_II": 1,
    "GBA1-related_disorder|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_provided|not_specified|Gaucher_disease": 1,
    "Gaucher_disease_type_II|not_provided": 1,
    "not_specified|Gaucher_disease_type_I|not_provided": 1,
    "not_specified|not_provided|Lewy_body_dementia|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I": 1,
    "Gaucher_disease_type_I|not_specified": 3,
    "Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided|not_specified": 1,
    "Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|not_specified": 1,
    "GBA-related_disorder|Gaucher_disease|Gaucher_disease_type_I|Gaucher_disease_type_III|not_provided|Gaucher_disease_type_II|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome": 1,
    "Parkinsonian_disorder|Thoracolumbar_scoliosis|Hypomimic_face|Movement_disorder|Resting_tremor|GBA1-related_disorder|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_specified|not_provided|Gaucher_disease|Dementia|_Lewy_body|_susceptibility_to": 1,
    "Gaucher_disease|not_specified": 4,
    "Lewy_body_dementia|Gaucher_disease_type_III|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_perinatal_lethal|not_specified|not_provided|Gaucher_disease": 1,
    "Lewy_body_dementia": 7,
    "Lewy_body_dementia|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I": 1,
    "Gaucher_disease_type_II": 3,
    "not_provided|Gaucher_disease": 13,
    "Gaucher_disease_type_II|Gaucher_disease_type_I|Lewy_body_dementia|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided": 1,
    "Gaucher_disease|Gaucher_disease_type_III|Gaucher_disease_type_I": 1,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Lewy_body_dementia|Parkinson_disease|_late-onset|not_provided|Gaucher_disease": 2,
    "Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III": 1,
    "Gaucher_disease|not_provided": 6,
    "Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|not_provided|Gaucher_disease": 2,
    "Gaucher_disease_perinatal_lethal|not_provided": 2,
    "not_specified|not_provided|Resting_tremor|Cogwheel_rigidity|Parkinsonian_disorder": 1,
    "Gaucher_disease_type_I|GBA1-related_disorder": 1,
    "Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided|Gaucher_disease": 1,
    "Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|not_provided|Gaucher_disease|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_provided|Gaucher_disease|Gaucher_disease_type_I": 3,
    "Parkinson_disease|_late-onset|Lewy_body_dementia|GBA1-related_disorder|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_specified|not_provided|Parkinson_disease|Gaucher_disease|Dementia|_Lewy_body|_susceptibility_to|Thrombocytopenia|Abnormal_bleeding|Akinesia|Rigidity": 1,
    "not_provided|Gaucher_disease_type_I|Gaucher_disease_perinatal_lethal|Gaucher_disease|not_specified": 1,
    "not_specified|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Parkinson_disease|_late-onset|not_provided|Gaucher_disease": 1,
    "not_specified|not_provided|Gaucher_disease|Parkinson_disease|_late-onset|Gaucher_disease_perinatal_lethal": 1,
    "not_provided|not_specified|Gaucher_disease": 1,
    "Gaucher_disease_type_I|not_provided": 2,
    "not_specified|Gaucher_disease_type_I|Lewy_body_dementia|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Hepatoblastoma": 1,
    "Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|not_provided|Gaucher_disease": 2,
    "not_provided|not_specified|Gaucher_disease|Gaucher_disease_type_I": 1,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_perinatal_lethal": 1,
    "Gaucher_disease_type_III": 2,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|not_provided|Gaucher_disease": 3,
    "not_provided|GBA1-related_disorder": 1,
    "not_provided|GBA1-related_disorder|Gaucher_disease_type_I|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_II|Gaucher_disease_type_III|not_specified|Gaucher_disease": 1,
    "not_specified|not_provided|Gaucher_disease|Parkinson_disease|_late-onset|Gaucher_disease_perinatal_lethal|Rigidity|Parkinsonian_disorder|Cogwheel_rigidity|Tremor|Hyperlipidemia|Abnormal_speech_pattern|Hypertensive_disorder|Dementia|Lower_limb_muscle_weakness": 1,
    "not_specified|not_provided|Gaucher_disease_type_I|Gaucher_disease": 1,
    "Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_provided|Gaucher_disease": 2,
    "not_specified|not_provided|Gaucher_disease": 2,
    "Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Parkinson_disease|_late-onset|Gaucher_disease": 1,
    "not_specified|not_provided|Gaucher_disease_type_I": 1,
    "not_provided|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Parkinson_disease|_late-onset|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome": 2,
    "not_specified|Gaucher_disease": 2,
    "Gaucher_disease|Gaucher_disease_type_I|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_II|Gaucher_disease_type_III|not_provided": 1,
    "not_specified|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|not_provided|Parkinson_disease|_late-onset": 1,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided": 2,
    "Gaucher_disease|Parkinson_disease|_late-onset|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided": 1,
    "Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Parkinson_disease|_late-onset|Gaucher_disease": 1,
    "Gaucher_disease_type_I|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_II|Parkinson_disease|_late-onset|Lewy_body_dementia|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome": 1,
    "GBA1-related_disorder|not_provided|not_specified": 1,
    "GBA1-related_disorder|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_provided|Gaucher_disease": 1,
    "GBA1-related_disorder|not_specified|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided|Gaucher_disease": 1,
    "Parkinson_disease|_late-onset|not_provided": 5,
    "Parkinson_disease|_late-onset|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease": 1,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Lewy_body_dementia|Parkinson_disease|_late-onset|not_specified|not_provided": 1,
    "Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Gaucher_disease_type_I|Gaucher_disease_type_II|not_provided|not_specified|Gaucher_disease": 1,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_III|not_provided|Gaucher_disease|Parkinson_disease|_late-onset": 1,
    "Gaucher_disease|not_provided|not_specified": 1,
    "Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|not_specified|not_provided|Gaucher_disease": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 61,
    "not_provided|Gaucher_disease|Gaucher_disease_type_II|Gaucher_disease_type_I|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome": 1,
    "Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|not_specified|not_provided|Gaucher_disease": 1,
    "Gaucher_disease|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Parkinson_disease|_late-onset|not_provided": 1,
    "Gaucher_disease|Thrombocytopenia|Abnormal_bleeding|Gaucher_disease_type_I|Parkinson_disease|_late-onset": 1,
    "not_specified|not_provided|Gaucher_disease|Gaucher_disease_type_I": 2,
    "not_provided|Parkinson_disease|_late-onset|Gaucher_disease": 1,
    "not_provided|Gaucher_disease|Parkinson_disease|_late-onset|GBA1-related_disorder|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome": 1,
    "Gaucher_disease|Parkinson_disease|_late-onset|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|Gaucher_disease_perinatal_lethal|Gaucher_disease": 1,
    "Gaucher_disease_type_I|Gaucher_disease_perinatal_lethal": 1,
    "not_provided|Gaucher_disease|not_specified": 1,
    "Gaucher_disease_perinatal_lethal|Gaucher_disease": 1,
    "not_specified|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome": 1,
    "GBA1-related_disorder": 1,
    "Gaucher_disease|Gaucher_disease_type_I|not_provided": 1,
    "not_provided|Gaucher_disease_type_I": 2,
    "Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease|not_provided": 1,
    "Gaucher_disease_type_I|Gaucher_disease_perinatal_lethal|not_specified": 1,
    "Gaucher_disease|Lewy_body_dementia|Gaucher_disease_type_I": 1,
    "not_specified|Gaucher_disease|Gaucher_disease_type_I|not_provided": 1,
    "not_provided|Gaucher_disease|Gaucher_disease_type_III|Gaucher_disease_type_I": 1,
    "Gaucher_disease_type_I|Gaucher_disease": 1,
    "Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|not_provided|Gaucher_disease|See_cases": 1,
    "not_provided|Gaucher_disease_type_I|Gaucher_disease": 1,
    "not_specified|not_provided|Lewy_body_dementia|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease": 1,
    "Gaucher_disease|not_specified|Parkinson_disease|_late-onset": 1,
    "GBA1-related_disorder|Gaucher_disease|Lewy_body_dementia|Parkinson_disease|_late-onset|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|not_provided": 1,
    "not_specified|not_provided|Gaucher_disease|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Parkinson_disease|_late-onset": 1,
    "not_provided|Gaucher_disease_perinatal_lethal": 1,
    "not_specified|Lewy_body_dementia": 1,
    "Young-onset_Parkinson_disease|not_specified|Gaucher_disease|Parkinson_disease|_late-onset|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Lewy_body_dementia|not_provided": 1,
    "not_specified|Gaucher_disease_perinatal_lethal|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Lewy_body_dementia|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Parkinson_disease|_late-onset|Gaucher_disease": 1,
    "GBA1-related_disorder|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I|Gaucher_disease_type_II|Gaucher_disease_type_III|Lewy_body_dementia|Gaucher_disease_perinatal_lethal|Parkinson_disease|_late-onset|not_provided|Gaucher_disease": 1,
    "Gaucher_disease_type_III|Gaucher_disease_type_II|Parkinson_disease|_late-onset|Gaucher_disease_perinatal_lethal|Lewy_body_dementia|Gaucher_disease-ophthalmoplegia-cardiovascular_calcification_syndrome|Gaucher_disease_type_I": 1,
    "not_provided|Thrombocytopenia|Abnormal_bleeding": 3,
    "not_provided|Gaucher_disease|GBA1-related_disorder": 1,
    "Pyruvate_kinase_deficiency_of_red_cells": 64,
    "not_provided|Pyruvate_kinase_deficiency_of_red_cells": 25,
    "Pyruvate_kinase_deficiency_of_red_cells|not_provided": 20,
    "not_provided|not_specified|Pyruvate_kinase_deficiency_of_red_cells": 2,
    "not_provided|Pyruvate_kinase_deficiency_of_red_cells|not_specified": 1,
    "PKLR-related_disorder|not_provided": 8,
    "Pyruvate_kinase_deficiency_of_red_cells|not_specified|not_provided": 1,
    "Pyruvate_kinase_hyperactivity|Pyruvate_kinase_deficiency_of_red_cells|not_provided": 3,
    "not_provided|Pyruvate_kinase_deficiency_of_red_cells|PKLR-related_disorder": 2,
    "Congenital_anemia|PKLR-related_disorder|not_provided|Pyruvate_kinase_deficiency_of_red_cells": 1,
    "PKLR-related_disorder": 8,
    "PKLR-related_disorder|Pyruvate_kinase_deficiency_of_red_cells|Pyruvate_kinase_hyperactivity|not_provided": 1,
    "not_provided|Pyruvate_kinase_hyperactivity": 1,
    "PKLR-related_disorder|Pyruvate_kinase_deficiency_of_red_cells|Pyruvate_kinase_hyperactivity|not_provided|See_cases": 1,
    "Pyruvate_kinase_deficiency_of_red_cells|not_provided|Pyruvate_kinase_hyperactivity": 1,
    "Hemolytic_anemia|Pyruvate_kinase_deficiency_of_red_cells|not_provided": 1,
    "PKLR-related_disorder|Pyruvate_kinase_deficiency_of_red_cells|not_provided": 2,
    "not_provided|Pyruvate_kinase_hyperactivity|Pyruvate_kinase_deficiency_of_red_cells": 1,
    "not_provided|PKLR-related_disorder": 3,
    "Pyruvate_kinase_hyperactivity|Pyruvate_kinase_deficiency_of_red_cells": 1,
    "Pyruvate_kinase_hyperactivity": 2,
    "Congenital_anemia|not_provided": 1,
    "Pyruvate_kinase_deficiency_of_red_cells|Pyruvate_kinase_hyperactivity": 2,
    "not_provided|PKLR-related_disorder|Pyruvate_kinase_deficiency_of_red_cells": 2,
    "Inborn_genetic_diseases|Pyruvate_kinase_deficiency_of_red_cells": 1,
    "Pyruvate_kinase_deficiency_of_red_cells|Pyruvate_kinase_hyperactivity|not_provided": 1,
    "not_provided|Pyruvate_kinase_deficiency_of_red_cells|Inborn_genetic_diseases": 1,
    "Pyruvate_kinase_deficiency_of_red_cells|PKLR-related_disorder": 1,
    "response_to_aminobisphosphonates": 1,
    "FDPS-related_disorder": 5,
    "Porokeratosis_9|_multiple_types": 3,
    "not_provided|FDPS-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_52|Inborn_genetic_diseases|ASH1L-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_52": 156,
    "not_provided|ASH1L-related_disorder": 10,
    "Intellectual_disability|_autosomal_dominant_52|not_provided": 9,
    "ASH1L-related_disorder": 47,
    "ASH1L-related_disorder|not_provided": 11,
    "Intellectual_disability|ASH1L-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "See_cases|Intellectual_disability|_autosomal_dominant_52|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_52": 1,
    "Intellectual_disability|_autosomal_dominant_52|not_provided|Intellectual_disability": 1,
    "ASH1L-related_neurodevelopmental_disorders|Intellectual_disability|_autosomal_dominant_52": 2,
    "Syndromic_complex_neurodevelopmental_disorder": 3,
    "ASH1L-related_neurodevelopmental_disorders": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_52": 9,
    "Rare_genetic_intellectual_disability": 26,
    "not_provided|Inborn_genetic_diseases|ASH1L-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_52": 4,
    "ASH1L-related_disorder|Autism_spectrum_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_52|Global_developmental_delay": 1,
    "Intellectual_disability|_autosomal_dominant_52|Inborn_genetic_diseases|not_provided": 2,
    "ASH1L-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_52|Inborn_genetic_diseases": 11,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_52": 1,
    "Intellectual_disability|_autosomal_dominant_52|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|ASH1L-related_disorder": 1,
    "ASH1L-related_disorder|Intellectual_disability|_autosomal_dominant_52|not_provided": 2,
    "not_provided|ASH1L-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_52|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_52|ASH1L-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_52|ASH1L-related_neurodevelopmental_disorders": 1,
    "ASH1L-related_disorder|Intellectual_disability|_autosomal_dominant_52|Inborn_genetic_diseases": 1,
    "Syndromic_complex_neurodevelopmental_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Syndromic_complex_neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_52|ASH1L-related_disorder": 1,
    "not_provided|Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome": 5,
    "Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome": 18,
    "Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome": 2,
    "MSTO1-related_disorder|not_provided": 2,
    "Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|not_provided": 7,
    "Congenital_cerebellar_hypoplasia": 20,
    "MSTO1-related_disorder": 4,
    "Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|not_provided|Inborn_mitochondrial_myopathy": 1,
    "not_provided|MSTO1-related_disorder": 3,
    "Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|Inborn_mitochondrial_myopathy|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|not_provided": 2,
    "not_provided|Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|Inborn_genetic_diseases|See_cases": 1,
    "Neuromuscular_disease|Inborn_genetic_diseases": 1,
    "Mitochondrial_myopathy-cerebellar_ataxia-pigmentary_retinopathy_syndrome|Inborn_genetic_diseases": 1,
    "YY1AP1-related_disorder|not_provided": 5,
    "YY1AP1-related_disorder": 4,
    "Grange_syndrome": 15,
    "not_provided|YY1AP1-related_disorder|Inborn_genetic_diseases": 1,
    "YY1AP1-related_disorder|Grange_syndrome": 1,
    "YY1AP1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Perrault_syndrome_1|not_specified|Perrault_syndrome_7": 1,
    "See_cases|DAP3-related_disorder": 1,
    "Perrault_syndrome_1|Perrault_syndrome_7": 2,
    "GON4L-related_disorder": 22,
    "LI-TAKADA-MIYAKE_SYNDROME": 2,
    "not_provided|GON4L-related_disorder": 1,
    "RIT1-related_disorder|not_specified": 1,
    "Noonan_syndrome_8": 141,
    "Noonan_syndrome_8|not_provided|Cardiovascular_phenotype": 2,
    "Noonan_syndrome_8|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_8": 26,
    "not_specified|Noonan_syndrome_8": 3,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_8": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Noonan_syndrome_8|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_8|Cardiovascular_phenotype": 11,
    "not_provided|Noonan_syndrome_8|Cardiovascular_phenotype": 3,
    "not_specified|Noonan_syndrome_8|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_8": 2,
    "not_provided|Noonan_syndrome_8": 4,
    "RIT1-related_disorder|Noonan_syndrome_8": 1,
    "Noonan_syndrome_8|not_provided": 7,
    "Cardiovascular_phenotype|not_specified|Noonan_syndrome_8": 2,
    "Noonan_syndrome_8|not_specified|Cardiovascular_phenotype": 1,
    "RIT1-related_disorder|not_provided|Noonan_syndrome_8|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_8|Fibrous_dysplasia_of_jaw": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RIT1-related_disorder|Noonan_syndrome_8": 1,
    "Noonan_syndrome_8|not_specified": 9,
    "Noonan_syndrome_8|not_specified|not_provided": 1,
    "Noonan_syndrome_8|RIT1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardio-facio-cutaneous_syndrome|not_provided|Cardiovascular_phenotype|Noonan_syndrome_8": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_8|not_specified": 1,
    "RIT1-related_disorder": 3,
    "Noonan_syndrome_8|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_8|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Noonan_syndrome_8|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_8": 1,
    "Noonan_syndrome|Noonan_syndrome_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|RIT1-related_disorder|Noonan_syndrome_8|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome": 45,
    "Cardiovascular_phenotype|RIT1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_8|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Inborn_genetic_diseases|Noonan_syndrome_8|RASopathy|not_provided": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype|Noonan_syndrome_8|Noonan_syndrome_and_Noonan-related_syndrome|RIT1-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_8|RASopathy|Noonan_syndrome|not_provided": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_8|Noonan_syndrome": 1,
    "Noonan_syndrome_8|RIT1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_8|not_specified": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan_syndrome_8": 1,
    "not_specified|Cardiovascular_phenotype|Noonan_syndrome_8": 1,
    "RASopathy|Noonan_syndrome_8|Noonan_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Inborn_genetic_diseases|Noonan_syndrome_8|not_provided|Noonan_syndrome|RASopathy|Noonan_syndrome_1": 1,
    "RIT1-related_disorder|Noonan_syndrome|Congenital_heart_disease|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_8|not_provided|Non-immune_hydrops_fetalis|RASopathy": 1,
    "Noonan_syndrome_8|Noonan_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "RASopathy|Noonan_syndrome_8|not_provided|RIT1-related_disorder": 1,
    "Noonan_syndrome_1": 17,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_8|not_provided|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RIT1-related_disorder|Noonan_syndrome_8|not_provided|RASopathy|Noonan_syndrome": 1,
    "not_provided|Noonan_syndrome|Noonan_syndrome_8": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Inborn_genetic_diseases|RIT1-related_disorder|Noonan_syndrome_8|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "not_specified|not_provided|Noonan_syndrome_8": 1,
    "Noonan_syndrome|Noonan_syndrome_8|not_provided": 1,
    "Noonan_syndrome_8|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_8|Cardiovascular_phenotype|RIT1-related_disorder": 1,
    "Noonan_syndrome_1|Noonan_syndrome_8|not_provided": 1,
    "Noonan_syndrome_8|not_provided|Noonan_syndrome": 1,
    "RIT1-related_disorder|Noonan_syndrome_8|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_8|not_provided": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RIT1-related_disorder|Noonan_syndrome_8|RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Noonan_syndrome|Noonan_syndrome_8": 1,
    "Noonan_syndrome_8|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_8|Noonan_syndrome": 1,
    "Noonan_syndrome_8|Noonan_syndrome_1|not_provided": 1,
    "Noonan_syndrome_8|RIT1-related_disorder|not_specified|not_provided": 1,
    "RASopathy|Noonan_syndrome_8|not_provided|Noonan_syndrome": 1,
    "Noonan_syndrome_8|Noonan_syndrome_1|RIT1-related_disorder": 1,
    "Noonan_syndrome_8|not_provided|Noonan_syndrome_1": 1,
    "Noonan_syndrome_8|Hypertelorism|Pedal_edema|Downslanted_palpebral_fissures|Short_stature|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_8|Cardiovascular_phenotype|not_specified|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Noonan_syndrome_8|RIT1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_8|RIT1-related_disorder": 1,
    "not_specified|RIT1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_midbrain_and_hindbrain_malformations|not_provided": 4,
    "ARHGEF2-related_disorder": 7,
    "Neurodevelopmental_disorder_with_midbrain_and_hindbrain_malformations": 5,
    "not_provided|Neurodevelopmental_disorder_with_midbrain_and_hindbrain_malformations": 1,
    "not_provided|ARHGEF2-related_disorder": 1,
    "ARHGEF2-related_disorder|not_provided": 2,
    "not_specified|Neurodevelopmental_disorder_with_midbrain_and_hindbrain_malformations": 1,
    "Primary_immunodeficiency_syndrome_due_to_p14_deficiency|not_specified|not_provided": 1,
    "LAMTOR2-related_disorder|not_provided": 1,
    "not_provided|Primary_immunodeficiency_syndrome_due_to_p14_deficiency": 1,
    "Primary_immunodeficiency_syndrome_due_to_p14_deficiency|not_provided": 1,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Limb-girdle_muscular_dystrophy|_recessive|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_Cardiomyopathy|_Dominant|Familial_partial_lipodystrophy|Mandibuloacral_dysplasia|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy|not_provided|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Limb-girdle_muscular_dystrophy|_recessive|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hutchinson-Gilford_syndrome|Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy|Limb-girdle_muscular_dystrophy|_recessive|Familial_partial_lipodystrophy": 1,
    "Mandibuloacral_dysplasia|Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Lethal_tight_skin_contracture_syndrome|Familial_partial_lipodystrophy": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Lethal_tight_skin_contracture_syndrome": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Lethal_tight_skin_contracture_syndrome": 1,
    "Mandibuloacral_dysplasia|Charcot-Marie-Tooth_disease_type_2|Hutchinson-Gilford_syndrome|Lethal_tight_skin_contracture_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Emery-Dreifuss_muscular_dystrophy|Familial_partial_lipodystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Maturity_onset_diabetes_mellitus_in_young|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Lethal_tight_skin_contracture_syndrome|not_provided": 1,
    "Mandibuloacral_dysplasia|Charcot-Marie-Tooth_disease_type_2|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_Cardiomyopathy|_Dominant|Emery-Dreifuss_muscular_dystrophy|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Lethal_tight_skin_contracture_syndrome|Familial_partial_lipodystrophy": 1,
    "Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Lethal_tight_skin_contracture_syndrome|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy": 1,
    "LMNA-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hutchinson-Gilford_syndrome|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy|Mandibuloacral_dysplasia|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Familial_partial_lipodystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|not_provided|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Dilated_cardiomyopathy_1A|See_cases": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 30,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 17,
    "Charcot-Marie-Tooth_disease|not_specified|Primary_dilated_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 3,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 19,
    "Primary_dilated_cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Lipodystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|LMNA-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1": 9,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 33,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 101,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2": 3,
    "Charcot-Marie-Tooth_disease_type_2|Severe_muscular_hypotonia|Relative_macrocephaly|Developmental_regression": 1,
    "Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 6,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Cardiovascular_phenotype|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|not_provided|Cardiomyopathy": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Paroxysmal_familial_ventricular_fibrillation": 1,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2": 4,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation": 14,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 2,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A": 2,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Charcot-Marie-Tooth_disease_type_2|LMNA-related_disorder|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_provided": 1,
    "Congenital_muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 38,
    "Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided": 10,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_provided": 3,
    "Familial_partial_lipodystrophy|_Dunnigan_type|not_provided": 3,
    "not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 3,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy": 1,
    "Hutchinson-Gilford_syndrome": 13,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "not_provided|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|not_provided": 1,
    "not_provided|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Familial_partial_lipodystrophy|_Dunnigan_type": 2,
    "Primary_familial_dilated_cardiomyopathy": 40,
    "Charcot-Marie-Tooth_disease_type_2|Familial_partial_lipodystrophy|_Dunnigan_type|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 10,
    "not_specified|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 2,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 4,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy": 16,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 7,
    "not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 3,
    "Charcot-Marie-Tooth_disease_type_2|Heart-hand_syndrome|_Slovenian_type": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9": 578,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 6,
    "Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2": 4,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Hutchinson-Gilford_syndrome|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 2,
    "Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Heart-hand_syndrome|_Slovenian_type": 1,
    "Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 2,
    "Cardiovascular_phenotype|not_provided|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 22,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 6,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2B1|Limb-girdle_muscular_dystrophy|_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_provided|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Sick_sinus_syndrome": 2,
    "Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|Cardiomyopathy|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Dilated_cardiomyopathy_1A": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_familial_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Peripheral_neuropathy|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Dilated_cardiomyopathy_1A": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|not_specified|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 1,
    "LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2": 5,
    "Conduction_system_disorder": 3,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|not_provided": 5,
    "not_provided|Primary_dilated_cardiomyopathy": 51,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy": 1,
    "LMNA-related_disorder": 10,
    "Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type": 3,
    "not_provided|not_specified|Hutchinson-Gilford_syndrome": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy": 9,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy": 3,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 2,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Primary_familial_dilated_cardiomyopathy|not_provided": 5,
    "Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|LMNA-related_disorder|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "Hutchinson-Gilford_progeria_syndrome|_childhood-onset|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Dilated_cardiomyopathy_1A|not_provided": 4,
    "not_provided|Hutchinson-Gilford_progeria_syndrome|_childhood-onset": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hutchinson-Gilford_progeria_syndrome|_atypical|Hutchinson-Gilford_syndrome": 1,
    "not_specified|LMNA-related_disorder|Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 5,
    "Muscular_dystrophy": 20,
    "Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|LMNA-related_disorder": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Lethal_tight_skin_contracture_syndrome": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|not_provided": 1,
    "not_specified|Cardiomyopathy|Charcot-Marie-Tooth_disease|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type": 1,
    "not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2": 2,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2|Lethal_tight_skin_contracture_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1A": 6,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 91,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2|not_provided|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|not_provided": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy": 2,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|LMNA-related_disorder|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|not_provided|Familial_partial_lipodystrophy|_Dunnigan_type|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease|Lethal_tight_skin_contracture_syndrome": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided": 158,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Dilated_cardiomyopathy_1A": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 3,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 3,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|not_provided": 1,
    "Cardiovascular_phenotype|Laminopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Primary_familial_dilated_cardiomyopathy|not_provided|Atrioventricular_block": 1,
    "Cardiovascular_phenotype|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Laminopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Ventricular_tachycardia|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Abnormality_of_the_musculature": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 2,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Cardiomyopathy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_provided": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 2,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 2,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Laminopathy|Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_muscular_dystrophy|Cardiomyopathy|Abnormality_of_the_musculature": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|not_specified|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Early_onset_multivalvular_disease": 1,
    "Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2": 2,
    "not_provided|Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Lethal_tight_skin_contracture_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome|Limb-girdle_muscular_dystrophy|_recessive|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|Cardiomyopathy": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Lethal_tight_skin_contracture_syndrome": 1,
    "not_specified|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|LMNA-related_disorder|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Muscular_dystrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 2,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 2,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_specified|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Primary_dilated_cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease|Lethal_tight_skin_contracture_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Primary_dilated_cardiomyopathy|Myocarditis": 1,
    "not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 1,
    "Autosomal_recessive_axonal_hereditary_motor_and_sensory_neuropathy|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|LMNA-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Cardiomyopathy": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 1,
    "Lipodystrophy|not_provided|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A": 1,
    "Hutchinson-Gilford_progeria_syndrome|_atypical": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 3,
    "not_provided|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy_1S|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 1,
    "Right_ventricular_cardiomyopathy|Hutchinson-Gilford_progeria_syndrome|_childhood-onset": 1,
    "Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_specified": 1,
    "Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy|Mandibuloacral_dysplasia|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Lethal_tight_skin_contracture_syndrome|Familial_partial_lipodystrophy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Lethal_tight_skin_contracture_syndrome|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A": 1,
    "Cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Cardiovascular_phenotype|not_provided|Emery-Dreifuss_muscular_dystrophy|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A": 1,
    "Cardiovascular_phenotype|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type": 1,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 3,
    "not_specified|Mandibuloacral_dysplasia|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Emery-Dreifuss_muscular_dystrophy|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Lethal_tight_skin_contracture_syndrome": 1,
    "Lethal_tight_skin_contracture_syndrome|not_specified|Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|See_cases": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Laminopathy|Primary_dilated_cardiomyopathy|Primary_familial_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Left_ventricular_noncompaction|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Dehydrated_hereditary_stomatocytosis_2|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type": 1,
    "Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Primary_dilated_cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy": 1,
    "Primary_dilated_cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Monogenic_diabetes|Primary_dilated_cardiomyopathy|Laminopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|Muscular_dystrophy|not_provided|Emery-Dreifuss_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "not_provided|Muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Laminopathy": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Limb-girdle_muscular_dystrophy": 3,
    "Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Sudden_unexplained_death|Muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Neuromuscular_disease|Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1A": 1,
    "Muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy|Dilated_cardiomyopathy_1A|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_Cardiomyopathy|_Dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Lethal_tight_skin_contracture_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy": 3,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "LMNA-associated_condition": 1,
    "LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Proximal_muscle_weakness": 5,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided": 3,
    "Dilated_cardiomyopathy_1D": 12,
    "Charcot-Marie-Tooth_disease_type_2|Family_history_of_sudden_cardiac_death|Collapse_(finding)|not_provided|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|not_provided|not_specified": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|not_provided": 9,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiomyopathy": 1,
    "Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_specified|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|not_provided|Charcot-Marie-Tooth_disease|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Polyneuropathy": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Mandibuloacral_dysplasia": 2,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_specified|Cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|not_provided|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome": 1,
    "Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|_atypical|Cardiomyopathy|not_specified|not_provided|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Emery-Dreifuss_muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|not_provided|Lethal_tight_skin_contracture_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_specified|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Cardiomyopathy|Primary_dilated_cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease|Lethal_tight_skin_contracture_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Abnormality_of_the_musculature": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome|Primary_dilated_cardiomyopathy|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|not_provided|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Primary_dilated_cardiomyopathy|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Cardiomyopathy|not_specified|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Primary_dilated_cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2|not_provided": 2,
    "Dilated_cardiomyopathy_1A|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|_atypical|not_provided": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Familial_partial_lipodystrophy|not_provided": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Monogenic_diabetes|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Lethal_tight_skin_contracture_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Laminopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1": 1,
    "Cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|LMNA-related_disorder": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Lethal_tight_skin_contracture_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Restrictive_dermopathy_2|Cardiovascular_phenotype|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Emery-Dreifuss_muscular_dystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_specified|Lethal_tight_skin_contracture_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "LMNA-related_disorder|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Lethal_tight_skin_contracture_syndrome": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_familial_dilated_cardiomyopathy": 1,
    "Monogenic_diabetes|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Hereditary_liability_to_pressure_palsies|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Congenital_muscular_dystrophy": 4,
    "Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy_1A": 1,
    "Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Lethal_tight_skin_contracture_syndrome": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Left_ventricular_noncompaction|Cardiomyopathy|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Primary_dilated_cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Mandibuloacral_dysplasia|not_provided|Cardiomyopathy|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|_atypical|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Abnormality_of_the_musculature": 1,
    "not_specified|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided|Lethal_tight_skin_contracture_syndrome|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease|Emery-Dreifuss_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_provided|Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 1,
    "not_provided|Cardiovascular_phenotype|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiomyopathy": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 18,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Neuromuscular_disease|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome": 1,
    "Primary_dilated_cardiomyopathy|Heart-hand_syndrome|_Slovenian_type|not_provided": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hutchinson-Gilford_syndrome": 4,
    "Laminopathy|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1A": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_muscular_dystrophy|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Bethlem_myopathy_1A": 583,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Monogenic_diabetes|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|LMNA-related_disorder|Autosomal_semi-dominant_severe_lipodystrophic_laminopathy|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome|Hypercholesterolemia|Short_stature|2-3_finger_cutaneous_syndactyly|Microretrognathia|Decreased_body_weight|Microtia|Round_ear|Peripheral_neuropathy|Lipodystrophy": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Primary_dilated_cardiomyopathy": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified|LMNA-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2B1|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Limb-girdle_muscular_dystrophy|_recessive|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Primary_dilated_cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Laminopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease|not_provided|Cardiomyopathy|Cardiovascular_phenotype|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|LMNA-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Cardiomyopathy|Monogenic_diabetes|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_provided|Long_QT_syndrome|not_specified": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2": 1,
    "not_provided|Cardiomyopathy|not_specified": 8,
    "Lethal_tight_skin_contracture_syndrome|Limb-girdle_muscular_dystrophy|_recessive|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy": 1,
    "Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules|Emery-Dreifuss_muscular_dystrophy": 1,
    "Familial_partial_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|Mandibuloacral_dysplasia|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Lethal_tight_skin_contracture_syndrome|Emery-Dreifuss_muscular_dystrophy|Lipoatrophy_with_Diabetes|_Hepatic_Steatosis|_Hypertrophic_Cardiomyopathy|_and_Leukomelanodermic_Papules": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy": 1,
    "LMNA-related_disorder|not_specified|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy": 1,
    "Cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome": 1,
    "Cardiovascular_phenotype|Familial_partial_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|_atypical|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Cardiomyopathy|not_provided|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 3,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiovascular_phenotype|Familial_partial_lipodystrophy|_Dunnigan_type|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Hutchinson-Gilford_syndrome|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|Wolff-Parkinson-White_pattern": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 3,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "LMNA-related_disorder|Charcot-Marie-Tooth_disease|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Muscular_dystrophy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Cardiomyopathy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Restrictive_dermopathy_2|Hutchinson-Gilford_syndrome|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiomyopathy|LMNA-related_disorder|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Heart-hand_syndrome|_Slovenian_type|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease|Primary_dilated_cardiomyopathy|LMNA-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2B1|Restrictive_dermopathy_2|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|not_provided|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|not_provided|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Cardiovascular_phenotype|Cardiomyopathy|LMNA-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Hutchinson-Gilford_syndrome|Cardiovascular_phenotype|not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2|not_provided|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy|Hutchinson-Gilford_syndrome|Charcot-Marie-Tooth_disease_type_2B1|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Metabolic_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Restrictive_dermopathy_2|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy": 1,
    "LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy|Familial_partial_lipodystrophy|_Dunnigan_type": 1,
    "LMNA-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease_type_2B1|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Monogenic_diabetes|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Cardiomyopathy|Variant_of_unknown_significance|Primary_dilated_cardiomyopathy": 1,
    "Restrictive_dermopathy_2|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Heart-hand_syndrome|_Slovenian_type|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Hutchinson-Gilford_syndrome|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Congenital_muscular_dystrophy|Cardiomyopathy|Lethal_tight_skin_contracture_syndrome": 1,
    "LMNA-related_disorder|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Familial_partial_lipodystrophy|_Dunnigan_type|Primary_dilated_cardiomyopathy|Charcot-Marie-Tooth_disease_type_2|Heart-hand_syndrome|_Slovenian_type|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Charcot-Marie-Tooth_disease_type_2B1|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Charcot-Marie-Tooth_disease_type_2|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy": 1,
    "Hutchinson-Gilford_syndrome|Hutchinson-Gilford_progeria_syndrome|_atypical": 2,
    "Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|not_provided": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_2B1|Heart-hand_syndrome|_Slovenian_type|Familial_partial_lipodystrophy|_Dunnigan_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Hutchinson-Gilford_syndrome|Restrictive_dermopathy_2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Heart-hand_syndrome|_Slovenian_type|Hutchinson-Gilford_syndrome|Familial_partial_lipodystrophy|_Dunnigan_type|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Restrictive_dermopathy_2|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Primary_dilated_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Restrictive_dermopathy_2|Emery-Dreifuss_muscular_dystrophy_3|_autosomal_recessive|Mandibuloacral_dysplasia_with_type_A_lipodystrophy|Congenital_muscular_dystrophy_due_to_LMNA_mutation|Familial_partial_lipodystrophy|_Dunnigan_type|Hutchinson-Gilford_syndrome|Heart-hand_syndrome|_Slovenian_type|Dilated_cardiomyopathy-hypergonadotropic_hypogonadism_syndrome|Dilated_cardiomyopathy_1A|Charcot-Marie-Tooth_disease_type_2B1|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant|Charcot-Marie-Tooth_disease_type_2|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|not_specified": 150,
    "not_provided|Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Cone-rod_dystrophy_10": 2,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|Cone-rod_dystrophy_10": 5,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10|not_provided": 2,
    "SEMA4A-related_disorder": 2,
    "Retinitis_Pigmentosa|_Recessive|not_provided|Cone-rod_dystrophy_10|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_Pigmentosa|_Recessive|Cone-rod_dystrophy_10": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_specified|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|Cone-rod_dystrophy_10": 1,
    "not_provided|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_specified": 3,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10": 2,
    "not_specified|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided": 3,
    "Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_10": 1,
    "not_provided|Cone-rod_dystrophy_10|Retinitis_pigmentosa_35": 5,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|Polyp_of_colon|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|Cone-rod_dystrophy_10": 4,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10|Retinal_dystrophy|not_specified": 1,
    "Retinitis_pigmentosa_35": 2,
    "not_provided|Cone-rod_dystrophy_10|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive": 1,
    "SEMA4A-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa_35": 2,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided": 3,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa": 5,
    "Helicoid_peripapillary_chorioretinal_degeneration": 4,
    "not_provided|Cone-rod_dystrophy_10|Retinitis_pigmentosa": 1,
    "not_provided|SEMA4A-related_disorder": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10": 1,
    "not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Cone-rod_dystrophy_10": 1,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa_35|not_provided|Cone-Rod_Dystrophy|_Recessive|Retinitis_Pigmentosa|_Recessive|not_specified": 1,
    "Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10": 4,
    "Colorectal_cancer|Retinal_dystrophy|Optic_atrophy|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_10": 1,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa_35|not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa": 4,
    "Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_10|Retinitis_pigmentosa_35": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Colorectal_cancer|not_provided|Retinitis_pigmentosa_35|not_specified|Cone-rod_dystrophy_10": 1,
    "Retinal_dystrophy|not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|Retinitis_pigmentosa|not_specified": 1,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10|not_provided|SEMA4A-related_disorder": 1,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa_35|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|not_specified|Cone-rod_dystrophy_10": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|not_specified": 1,
    "Retinitis_pigmentosa_35|not_specified|not_provided|Cone-rod_dystrophy_10": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Cone-rod_dystrophy_10|Retinitis_pigmentosa_35": 1,
    "Retinitis_pigmentosa_35|Cone-rod_dystrophy_10|not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|not_specified|Retinal_dystrophy": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|Cone-rod_dystrophy_10|Retinitis_pigmentosa_35|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy": 1,
    "Cone-rod_dystrophy_10|Retinal_dystrophy|Retinitis_pigmentosa_35|not_provided": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_10|SEMA4A-related_disorder|not_provided": 1,
    "Cone-rod_dystrophy_10|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive": 1,
    "Cone-rod_dystrophy_10|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa": 4,
    "Cone-rod_dystrophy_10|not_provided|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_10|not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa": 1,
    "Nephrolithiasis|_calcium_oxalate": 27,
    "Neurodevelopmental_disorder_with_speech_or_visual_impairment_and_brain_hypomyelination|See_cases": 1,
    "Neurodevelopmental_disorder_with_speech_or_visual_impairment_and_brain_hypomyelination": 2,
    "not_specified|Neurodevelopmental_disorder_with_speech_or_visual_impairment_and_brain_hypomyelination": 1,
    "MEF2D-related_disorder": 1,
    "IQGAP3-related_disorder": 31,
    "not_specified|IQGAP3-related_disorder": 1,
    "Motor_and_sensory_neuropathy": 1,
    "IQGAP3-related_disorder|not_provided": 1,
    "not_provided|IQGAP3-related_disorder": 2,
    "not_provided|Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1": 9,
    "NAXE-related_disorder": 2,
    "Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy": 7,
    "NAXE-related_disorder|not_provided": 2,
    "Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1": 10,
    "Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|not_provided|NAXE-related_disorder|Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1": 1,
    "Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1|not_provided": 1,
    "Inborn_genetic_diseases|Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1|not_provided": 1,
    "Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1|Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy": 1,
    "not_specified|Congenital_fibrosis_of_extraocular_muscles": 1,
    "MRPL24-related_condition": 1,
    "Papillary_renal_cell_carcinoma_type_1": 206,
    "YOLK_SAC_TUMOR_AND_HIGH-GRADE_IMMATURE_TERATOMA": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_specified": 3,
    "NTRK1-related_disorder": 4,
    "not_provided|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency": 1,
    "not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 37,
    "Hereditary_insensitivity_to_pain_with_anhidrosis": 1038,
    "not_provided|Familial_medullary_thyroid_carcinoma": 3,
    "Familial_medullary_thyroid_carcinoma": 3,
    "Inborn_genetic_diseases|Hereditary_insensitivity_to_pain_with_anhidrosis": 40,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases|not_provided|NTRK1-related_disorder": 1,
    "Inborn_genetic_diseases|NTRK1-related_disorder|not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 3,
    "Inborn_genetic_diseases|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 9,
    "not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified": 3,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|not_provided": 22,
    "Inborn_genetic_diseases|NTRK1-related_disorder|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 2,
    "not_provided|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis": 2,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases": 46,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified": 8,
    "not_provided|Inborn_genetic_diseases|Hereditary_insensitivity_to_pain_with_anhidrosis": 7,
    "Inborn_genetic_diseases|Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified": 2,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Charcot-Marie-Tooth_disease": 8,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Familial_medullary_thyroid_carcinoma": 2,
    "not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases": 5,
    "Familial_medullary_thyroid_carcinoma|Hereditary_insensitivity_to_pain_with_anhidrosis": 3,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases|not_provided": 9,
    "PAIN_SENSITIVITY_QUANTITATIVE_TRAIT_LOCUS_1|Charcot-Marie-Tooth_disease|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases|not_specified": 3,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Hereditary_cancer|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Familial_medullary_thyroid_carcinoma|NTRK1-related_disorder|Inborn_genetic_diseases|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis": 5,
    "NTRK1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 2,
    "NTRK1-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|Hereditary_insensitivity_to_pain_with_anhidrosis|not_provided": 4,
    "not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy": 2,
    "Familial_medullary_thyroid_carcinoma|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 2,
    "not_provided|NTRK1-related_disorder|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "not_specified|NTRK1-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_cancer|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|NTRK1-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|NTRK1-related_disorder|not_specified": 1,
    "not_provided|Hereditary_cancer|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|NTRK1-related_disorder": 2,
    "NTRK1-related_disorder|not_provided|not_specified|Inborn_genetic_diseases|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis|NTRK1-related_disorder": 1,
    "Inborn_genetic_diseases|NTRK1-related_disorder|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis": 2,
    "NTRK1-related_disorder|Hereditary_insensitivity_to_pain_with_anhidrosis": 4,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases|Familial_medullary_thyroid_carcinoma": 1,
    "NTRK1-related_disorder|Inborn_genetic_diseases|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis|not_provided": 2,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|Familial_medullary_thyroid_carcinoma|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_insensitivity_to_pain_with_anhidrosis": 3,
    "Familial_medullary_thyroid_carcinoma|Hereditary_insensitivity_to_pain_with_anhidrosis|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|not_provided|Familial_medullary_thyroid_carcinoma|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "not_provided|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis|Familial_medullary_thyroid_carcinoma": 1,
    "Familial_medullary_thyroid_carcinoma|not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Pyruvate_kinase_deficiency_of_red_cells|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|NTRK1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|Familial_medullary_thyroid_carcinoma|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "not_specified|Premature_ovarian_failure|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis|Familial_medullary_thyroid_carcinoma": 1,
    "Hereditary_insensitivity_to_pain_with_anhidrosis|NTRK1-related_disorder|not_provided": 1,
    "NTRK1-related_disorder|not_specified|not_provided|Hereditary_insensitivity_to_pain_with_anhidrosis": 1,
    "NTRK1-related_disorder|not_specified": 1,
    "ETV3L-related_disorder": 4,
    "not_provided|ETV3L-related_disorder": 1,
    "Non-immune_hydrops_fetalis|not_specified": 2,
    "Nephrotic_syndrome|_type_23": 4,
    "KIRREL1-related_disorder": 21,
    "KIRREL1-related_disorder|not_specified|not_provided": 1,
    "not_specified|KIRREL1-related_disorder": 2,
    "not_specified|Nephrotic_syndrome|_type_23": 1,
    "Nephrotic_syndrome|_type_23|not_specified": 1,
    "Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 31,
    "Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|Elliptocytosis": 8,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary": 27,
    "not_provided|Elliptocytosis_2|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary": 20,
    "Pyropoikilocytosis|_hereditary|Elliptocytosis_2|Hereditary_spherocytosis_type_3|not_provided": 3,
    "Spherocytosis|_Recessive|Elliptocytosis|Pyropoikilocytosis|_hereditary": 2,
    "Pyropoikilocytosis|_hereditary|Spherocytosis|_Recessive|Elliptocytosis": 2,
    "Spherocytosis|_Recessive|not_provided|Elliptocytosis|Pyropoikilocytosis|_hereditary": 1,
    "not_provided|Spherocytosis|_Recessive|Elliptocytosis|Pyropoikilocytosis|_hereditary": 2,
    "Pyropoikilocytosis|_hereditary|Elliptocytosis_2|Hereditary_spherocytosis_type_3": 13,
    "Hereditary_spherocytosis_type_3|not_provided|Elliptocytosis_2|not_specified|Pyropoikilocytosis|_hereditary": 2,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "SPTA1-related_disorder": 16,
    "Pyropoikilocytosis|_hereditary|not_provided|Elliptocytosis_2|Hereditary_spherocytosis_type_3|not_specified|SPTA1-related_disorder": 1,
    "not_specified|Hereditary_spherocytosis_type_3|not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 3,
    "Elliptocytosis_2": 16,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_3|not_provided|Pyropoikilocytosis|_hereditary": 6,
    "not_specified|Hereditary_spherocytosis_type_3|Elliptocytosis_2|not_provided|Pyropoikilocytosis|_hereditary": 1,
    "Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|Elliptocytosis_2": 3,
    "SPTA1-related_disorder|not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 3,
    "not_specified|not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 6,
    "not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 20,
    "not_specified|not_provided|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 2,
    "not_provided|Elliptocytosis_2": 4,
    "not_specified|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_provided": 1,
    "not_provided|Elliptocytosis_2|Hereditary_spherocytosis_type_3|Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|Elliptocytosis": 1,
    "Pyropoikilocytosis|_hereditary|Spherocytosis|_Recessive|not_specified|not_provided|Elliptocytosis": 1,
    "Pyropoikilocytosis|_hereditary|Spherocytosis|_Recessive|Elliptocytosis|not_provided": 1,
    "not_provided|Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|Elliptocytosis|Hereditary_spherocytosis_type_3|Elliptocytosis_2|not_specified": 1,
    "Hereditary_spherocytosis|Hereditary_spherocytosis_type_3": 1,
    "not_specified|not_provided|Elliptocytosis_2|Familial_hemolytic_anemia": 1,
    "Hereditary_spherocytosis_type_3|not_provided": 7,
    "not_specified|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3": 1,
    "not_specified|Elliptocytosis_2": 2,
    "Hereditary_spherocytosis_type_3|Elliptocytosis_2|not_provided|Pyropoikilocytosis|_hereditary": 3,
    "Familial_hemolytic_anemia": 8,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided": 5,
    "not_provided|Hereditary_spherocytosis_type_3|Hemolytic_anemia|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_specified": 1,
    "Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided|Hereditary_spherocytosis_type_3": 3,
    "SPTA1-related_disorder|not_specified|not_provided": 2,
    "not_specified|not_provided|Hemolytic_anemia|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|not_specified|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_specified": 4,
    "Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|not_provided": 4,
    "Pyropoikilocytosis|_hereditary": 4,
    "not_provided|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|SPTA1-related_disorder": 1,
    "Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_provided": 9,
    "Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3": 2,
    "SPTA1-related_disorder|not_provided": 3,
    "not_provided|SPTA1-related_disorder": 9,
    "Hereditary_spherocytosis_type_3|not_provided|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 4,
    "Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|not_provided|Elliptocytosis": 1,
    "Spherocytosis|_Recessive|Elliptocytosis|not_provided|Pyropoikilocytosis|_hereditary": 1,
    "not_provided|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_specified": 4,
    "not_provided|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 7,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided|not_specified": 2,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_provided": 3,
    "Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|Elliptocytosis|not_provided": 1,
    "Pyropoikilocytosis|_hereditary|not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2": 1,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|SPTA1-related_disorder": 1,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_3|not_specified|not_provided|Pyropoikilocytosis|_hereditary|SPTA1-related_disorder": 1,
    "Intellectual_developmental_disorder|_X-linked_111|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|not_provided|not_specified|Hemolytic_anemia": 1,
    "not_specified|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|Elliptocytosis_2|not_provided": 1,
    "not_provided|Pyropoikilocytosis|_hereditary": 3,
    "Abnormality_of_blood_and_blood-forming_tissues": 5,
    "not_specified|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided": 3,
    "SPTA1-related_disorder|Hereditary_spherocytosis_type_3": 1,
    "not_provided|Hereditary_spherocytosis_type_3": 5,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_provided|not_specified|Elliptocytosis_2": 1,
    "Elliptocytosis_2|not_provided": 3,
    "Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_specified|not_provided": 3,
    "Pyropoikilocytosis|_hereditary|not_provided": 1,
    "Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3": 1,
    "Pyropoikilocytosis|_hereditary|not_provided|Elliptocytosis_2|Hereditary_spherocytosis_type_3": 4,
    "Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_provided|Hereditary_spherocytosis_type_3": 3,
    "Hereditary_spherocytosis_type_3|not_provided|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_specified": 2,
    "Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_provided|not_specified": 5,
    "not_provided|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3": 1,
    "not_specified|not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|Hereditary_spherocytosis_type_3": 1,
    "Hereditary_spherocytosis_type_3|not_specified|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_provided": 1,
    "Hereditary_spherocytosis_type_3|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided|SPTA1-related_disorder|Hereditary_spherocytosis": 1,
    "Pyropoikilocytosis|_hereditary|not_provided|Hereditary_spherocytosis_type_3|not_specified|Elliptocytosis_2": 1,
    "Hemolytic_anemia": 5,
    "not_specified|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_provided|Elliptocytosis_2": 1,
    "not_specified|Elliptocytosis_2|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|not_provided": 1,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_specified|not_provided|Elliptocytosis_2": 1,
    "not_provided|not_specified|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 2,
    "Hereditary_spherocytosis_type_3|not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 2,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_provided|Elliptocytosis_2|not_specified": 1,
    "not_provided|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_specified|Elliptocytosis_2": 2,
    "Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|Elliptocytosis_2|not_provided": 2,
    "Hereditary_spherocytosis_type_3|SPTA1-related_disorder|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided": 1,
    "not_specified|not_provided|SPTA1-related_disorder": 1,
    "not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|Hereditary_spherocytosis_type_3": 1,
    "not_provided|Elliptocytosis_2|Hereditary_spherocytosis_type_3|not_specified|Pyropoikilocytosis|_hereditary|SPTA1-related_disorder": 1,
    "not_specified|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 1,
    "Hereditary_spherocytosis_type_3|not_provided|not_specified|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|SPHEROCYTOSIS|_TYPE_3|_AUTOSOMAL_RECESSIVE": 1,
    "not_specified|Pyropoikilocytosis|_hereditary|not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2": 1,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|not_specified|Elliptocytosis_2|not_provided": 1,
    "Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|not_provided|Elliptocytosis_2": 2,
    "Pyropoikilocytosis|_hereditary|Elliptocytosis_2|SPTA1-related_disorder|not_provided|Hereditary_spherocytosis_type_3": 1,
    "Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|Elliptocytosis|not_specified": 1,
    "not_specified|Hereditary_spherocytosis_type_3|not_provided|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "not_provided|Hereditary_spherocytosis_type_3|not_specified|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 2,
    "Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 1,
    "Anemia|not_provided|SPTA1-related_disorder": 1,
    "Hereditary_spherocytosis_type_3|not_specified|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided": 1,
    "not_provided|Hemolytic_anemia": 1,
    "not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2": 1,
    "not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|Hereditary_spherocytosis_type_3|not_specified": 1,
    "not_specified|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided|Hereditary_spherocytosis_type_3": 1,
    "SPTA1-related_disorder|Hereditary_spherocytosis_type_3|not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 1,
    "SPTA1-related_disorder|not_specified|not_provided|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "Pyropoikilocytosis|_hereditary|not_provided|Spherocytosis|_Recessive|Elliptocytosis": 3,
    "not_provided|Spherocytosis|_Recessive|Pyropoikilocytosis|_hereditary|Elliptocytosis": 1,
    "not_provided|Hereditary_spherocytosis_type_3|not_specified|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "not_specified|Elliptocytosis_2|not_provided": 1,
    "Hereditary_spherocytosis_type_3|not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|Familial_hemolytic_anemia": 1,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|SPTA1-related_disorder|not_provided": 1,
    "Hereditary_spherocytosis_type_3|Elliptocytosis_2|not_specified|Pyropoikilocytosis|_hereditary": 1,
    "not_provided|Hereditary_spherocytosis_type_3|SPTA1-related_disorder|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "SPTA1-related_disorder|Pyropoikilocytosis|_hereditary|Elliptocytosis_2|not_provided|Hereditary_spherocytosis_type_3": 1,
    "Spherocytosis|not_provided|Elliptocytosis_2": 1,
    "Elliptocytosis_2|not_specified": 1,
    "not_specified|SPTA1-related_disorder|not_provided": 1,
    "not_provided|not_specified|SPTA1-related_disorder": 2,
    "Elliptocytosis_2|Pyropoikilocytosis|_hereditary|not_provided": 1,
    "Lysinuric_protein_intolerance|not_provided": 9,
    "SPTA1-related_disorder|not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 2,
    "Elliptocytosis_2|Hereditary_spherocytosis_type_2": 1,
    "Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "Prenatal_anemia|SPTA1-related_disorder|not_provided|Hereditary_spherocytosis_type_3|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 1,
    "not_provided|Pyropoikilocytosis|_hereditary|Elliptocytosis_2": 1,
    "not_provided|SPTA1-related_disorder|Pyropoikilocytosis|_hereditary|Hereditary_spherocytosis_type_3|Elliptocytosis_2": 1,
    "Spherocytosis": 7,
    "not_specified|Hereditary_spherocytosis_type_3|Elliptocytosis_2|Pyropoikilocytosis|_hereditary": 1,
    "PYHIN1-related_disorder": 2,
    "AIM2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "AIM2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2FF": 3,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2FF|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_type_2FF|not_provided": 1,
    "ACKR1-related_disorder": 3,
    "White_blood_cell_count_quantitative_trait_locus_1|Resistance_to_Plasmodium_vivax_infection|DUFFY_BLOOD_GROUP_SYSTEM|_FY(a-b-)_PHENOTYPE": 1,
    "not_specified|ACKR1-related_disorder|DUFFY_BLOOD_GROUP_SYSTEM|_FYA/FYB_POLYMORPHISM|not_provided": 1,
    "Duffy_Blood_group_system": 1,
    "DUFFY_BLOOD_GROUP_SYSTEM|_FY(bwk)_PHENOTYPE|ACKR1-related_disorder|not_specified": 1,
    "DUFFY_BLOOD_GROUP_SYSTEM|_FY(a-b-)_PHENOTYPE": 1,
    "Inflammation": 1,
    "CRP-related_disorder": 3,
    "CRP-related_disorder|not_provided": 1,
    "not_specified|Heterotaxy|_visceral|_11|_autosomal|_with_male_infertility": 1,
    "Heterotaxy|_visceral|_11|_autosomal|_with_male_infertility": 4,
    "Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 55,
    "not_specified|not_provided|PIGM-related_disorder|Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 1,
    "PIGM-related_disorder|not_provided|Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 2,
    "not_provided|Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 4,
    "Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency|not_provided|not_specified": 1,
    "not_specified|Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 6,
    "PIGM-related_disorder": 2,
    "not_specified|not_provided|Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 1,
    "Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency|not_specified|not_provided": 2,
    "Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency|not_specified": 6,
    "Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency|PIGM-related_disorder": 2,
    "Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency|not_provided": 1,
    "not_provided|not_specified|Hypercoagulability_syndrome_due_to_glycosylphosphatidylinositol_deficiency": 1,
    "EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 35,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 46,
    "Seizures|_Sensorineural_Deafness|_Ataxia|_Intellectual_Disability|_and_Electrolyte_Imbalance_Syndrome|Nonsyndromic_Hearing_Loss|_Mixed|Pendred_syndrome": 5,
    "not_provided|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 4,
    "EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|EAST_syndrome": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|not_provided": 2,
    "not_provided|Seizures|_Sensorineural_Deafness|_Ataxia|_Intellectual_Disability|_and_Electrolyte_Imbalance_Syndrome|Nonsyndromic_Hearing_Loss|_Mixed|Pendred_syndrome": 3,
    "Seizures|_Sensorineural_Deafness|_Ataxia|_Intellectual_Disability|_and_Electrolyte_Imbalance_Syndrome|Nonsyndromic_Hearing_Loss|_Mixed|Pendred_syndrome|not_provided": 1,
    "Pendred_syndrome|Seizures|_Sensorineural_Deafness|_Ataxia|_Intellectual_Disability|_and_Electrolyte_Imbalance_Syndrome|Nonsyndromic_Hearing_Loss|_Mixed": 1,
    "EAST_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Pendred_syndrome|Nonsyndromic_Hearing_Loss|_Mixed|Seizures|_Sensorineural_Deafness|_Ataxia|_Intellectual_Disability|_and_Electrolyte_Imbalance_Syndrome": 1,
    "EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 4,
    "Episodic_kinesigenic_dyskinesia": 334,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "EAST_syndrome": 168,
    "EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|not_provided|EAST_syndrome": 1,
    "EAST_syndrome|not_provided": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Pendred_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "EAST_syndrome|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|EAST_syndrome|not_provided|Intellectual_disability|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|EAST_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|EAST_syndrome|not_provided|Intellectual_disability": 1,
    "not_specified|KCNJ10-related_disorder|not_provided|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Inborn_genetic_diseases|EAST_syndrome": 5,
    "not_provided|EAST_syndrome": 17,
    "not_provided|EAST_syndrome|Inborn_genetic_diseases": 1,
    "Peripheral_neuropathy": 91,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_specified|KCNJ10-related_disorder": 1,
    "EAST_syndrome|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|not_provided|Inborn_genetic_diseases|EAST_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|not_provided|EAST_syndrome|not_specified": 1,
    "EAST_syndrome|Seizure": 1,
    "Inborn_genetic_diseases|KCNJ10-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|EAST_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Pendred_syndrome": 1,
    "KCNJ10-related_disorder|not_provided|EAST_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|EAST_syndrome": 1,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 1,
    "SeSAME-like_syndrome|not_provided": 1,
    "EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|KCNJ10-related_disorder|not_provided": 1,
    "SeSAME-like_syndrome": 1,
    "EAST_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 2,
    "Inborn_genetic_diseases|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "KCNJ10-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|EAST_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|EAST_syndrome": 1,
    "Inborn_genetic_diseases|EAST_syndrome|not_provided": 2,
    "not_specified|not_provided|KCNJ10-related_disorder|EAST_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|EAST_syndrome|not_provided": 1,
    "not_provided|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|EAST_syndrome": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|EAST_syndrome": 1,
    "Inborn_genetic_diseases|EAST_syndrome|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_specified|KCNJ10-related_disorder|EAST_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|EAST_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|EAST_syndrome|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "EAST_syndrome|Inborn_genetic_diseases|not_provided|KCNJ10-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|EAST_syndrome": 1,
    "Inborn_genetic_diseases|EAST_syndrome|not_specified": 1,
    "not_specified|not_provided|KCNJ10-related_disorder|Inborn_genetic_diseases|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Bilateral_sensorineural_hearing_impairment|Spastic_diplegia|Microcephaly|Cerebellar_ataxia|Renal_tubular_dysfunction|EAST_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|EAST_syndrome|Pendred_syndrome": 1,
    "not_specified|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "EAST_syndrome|KCNJ10-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Pendred_syndrome|KCNJ10-related_disorder|not_provided": 1,
    "EAST_syndrome|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Seizure|EAST_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "Inborn_genetic_diseases|EAST_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|EAST_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KCNJ10-related_disorder|not_specified|not_provided|EAST_syndrome|Seizure|Autism|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|EAST_syndrome|Pendred_syndrome|not_provided": 1,
    "EAST_syndrome|Inborn_genetic_diseases|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "EAST_syndrome|KCNJ10-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified": 1,
    "Nonsyndromic_Hearing_Loss|_Mixed|Seizures|_Sensorineural_Deafness|_Ataxia|_Intellectual_Disability|_and_Electrolyte_Imbalance_Syndrome": 2,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 20,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_specified": 1,
    "Familial_hemiplegic_migraine": 670,
    "not_provided|Familial_hemiplegic_migraine": 38,
    "not_specified|Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2": 22,
    "not_specified|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|not_provided|Migraine|_familial_hemiplegic|_2": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_specified|Alternating_hemiplegia_of_childhood|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 1,
    "Inborn_genetic_diseases|Familial_hemiplegic_migraine": 19,
    "Familial_hemiplegic_migraine|not_provided": 77,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Familial_hemiplegic_migraine|Inborn_genetic_diseases|not_provided|not_specified|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2": 2,
    "not_provided|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 4,
    "not_provided|not_specified|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "not_provided|not_specified|Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 2,
    "not_specified|Familial_hemiplegic_migraine": 22,
    "Familial_hemiplegic_migraine|not_specified|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_1|not_provided|Migraine|_familial_hemiplegic|_2": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 1,
    "Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_specified|ATP1A2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_98|Familial_hemiplegic_migraine": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Migraine|_familial_hemiplegic|_2|not_provided|Alternating_hemiplegia_of_childhood_1|not_specified": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Migraine|_familial_hemiplegic|_2|Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases|ATP1A2-related_disorder|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine|not_provided|Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hemiplegic_migraine|not_specified": 1,
    "Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98": 2,
    "not_specified|Familial_hemiplegic_migraine|ATP1A2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_provided": 6,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 31,
    "ATP1A2-related_disorder": 14,
    "Familial_hemiplegic_migraine|not_provided|Inborn_genetic_diseases": 5,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 3,
    "Familial_hemiplegic_migraine|not_specified": 19,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Polymicrogyria": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases|ATP1A2-related_disorder|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine|not_specified|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_provided|not_specified": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_specified|not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 2,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 3,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Inborn_genetic_diseases": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 2,
    "Familial_hemiplegic_migraine|not_provided|Migraine|_familial_hemiplegic|_2": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "not_provided|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Alternating_hemiplegia_of_childhood_1|not_specified|Migraine|_familial_hemiplegic|_2": 1,
    "not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98": 1,
    "Familial_hemiplegic_migraine|ATP1A2-related_disorder|not_specified": 1,
    "Alternating_hemiplegia_of_childhood|Familial_hemiplegic_migraine": 7,
    "not_provided|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases|not_specified|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 1,
    "Developmental_and_epileptic_encephalopathy_98": 7,
    "ATP1A2-related_disorder|Familial_hemiplegic_migraine": 7,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Inborn_genetic_diseases|not_provided|Familial_hemiplegic_migraine": 1,
    "not_specified|Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|Periodic_paralysis|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia_deformation_sequence|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant": 1,
    "ATP1A2-related_disorder|Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_provided": 1,
    "Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 3,
    "not_provided|Familial_hemiplegic_migraine|ATP1A2-related_disorder|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_2": 1,
    "Familial_hemiplegic_migraine|Inborn_genetic_diseases": 14,
    "not_provided|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|not_specified": 2,
    "Familial_hemiplegic_migraine|ATP1A2-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy_98|not_provided|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|not_specified|ATP1A2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_specified": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|ATP1A2-related_disorder|not_provided|Familial_hemiplegic_migraine": 1,
    "Alternating_hemiplegia_of_childhood_1": 6,
    "Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 6,
    "Inborn_genetic_diseases|not_provided|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 1,
    "Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_1": 1,
    "Familial_hemiplegic_migraine|not_provided|ATP1A2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_98|ATP1A2-related_disorder|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|not_provided": 1,
    "Familial_hemiplegic_migraine|See_cases": 1,
    "Dysphasia|Hemiparesis|Headache": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "Developmental_and_epileptic_encephalopathy_98|Familial_hemiplegic_migraine|not_provided": 1,
    "Familial_hemiplegic_migraine|ATP1A2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_98": 1,
    "Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases|not_provided|Migraine|_familial_hemiplegic|_2": 1,
    "Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|not_specified|Migraine|_familial_hemiplegic|_2|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_98|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_98|not_specified": 1,
    "Familial_hemiplegic_migraine|not_specified|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Migraine|_familial_hemiplegic|_2|Inborn_genetic_diseases|Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|ATP1A2-related_disorder|Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Familial_hemiplegic_migraine|not_provided|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_2": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 3,
    "Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine|ATP1A2-related_disorder": 1,
    "Familial_hemiplegic_migraine|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 1,
    "not_provided|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Familial_hemiplegic_migraine": 2,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Familial_hemiplegic_migraine|not_provided|Alternating_hemiplegia_of_childhood_1|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_2": 1,
    "Familial_hemiplegic_migraine|not_provided|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|ATP1A2-related_disorder|Familial_hemiplegic_migraine": 1,
    "not_provided|ATP1A2-related_disorder|Familial_hemiplegic_migraine|not_specified": 1,
    "Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_provided": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|not_provided|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "not_specified|Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_specified|Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "not_provided|ATP1A2-related_disorder|Familial_hemiplegic_migraine|Inborn_genetic_diseases": 1,
    "Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "not_specified|ATP1A2-related_disorder|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|not_provided|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Inborn_genetic_diseases|not_specified|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|ATP1A2-related_disorder|not_provided|Migraine|_familial_hemiplegic|_2": 1,
    "Inborn_genetic_diseases|ATP1A2-related_disorder|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Familial_hemiplegic_migraine|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_provided": 1,
    "not_provided|Familial_hemiplegic_migraine|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98": 1,
    "Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_provided|Familial_hemiplegic_migraine": 1,
    "Migraine|_familial_hemiplegic|_2|Developmental_and_epileptic_encephalopathy_98|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Familial_hemiplegic_migraine": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 1,
    "ATP1A2-related_disorder|Inborn_genetic_diseases|not_provided|Familial_hemiplegic_migraine": 1,
    "Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|not_provided|Alternating_hemiplegia_of_childhood_1": 1,
    "Developmental_and_epileptic_encephalopathy_98|ATP1A2-related_disorder|Familial_hemiplegic_migraine|not_provided|Migraine|_familial_hemiplegic|_2|Migraine|_familial_basilar": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified|Alternating_hemiplegia_of_childhood_1|not_provided|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 1,
    "not_provided|not_specified|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|not_specified": 1,
    "Familial_hemiplegic_migraine|not_specified|not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|not_provided": 1,
    "not_provided|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_1|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified|not_provided|Migraine|_familial_hemiplegic|_2": 1,
    "Familial_hemiplegic_migraine|Inborn_genetic_diseases|not_provided": 2,
    "ATP1A2-associated_neurological_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Familial_hemiplegic_migraine": 3,
    "ATP1A2-related_disorder|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Inborn_genetic_diseases|Familial_hemiplegic_migraine|ATP1A2-related_disorder|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "not_provided|Epileptic_encephalopathy|Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Inborn_genetic_diseases": 1,
    "not_provided|ATP1A2-related_disorder|Familial_hemiplegic_migraine": 1,
    "Inborn_genetic_diseases|not_provided|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|not_provided": 1,
    "Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 3,
    "Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "not_specified|not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Familial_hemiplegic_migraine|not_specified|Inborn_genetic_diseases": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|Inborn_genetic_diseases": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2": 2,
    "Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_specified|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_specified": 1,
    "Migraine|_familial_hemiplegic|_2|not_provided|Familial_hemiplegic_migraine": 1,
    "Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|not_provided|Familial_hemiplegic_migraine|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_specified|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3": 87,
    "not_provided|Familial_hemiplegic_migraine|ATP1A2-related_disorder": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy_98|not_provided|Migraine|_familial_hemiplegic|_2": 2,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2|Familial_hemiplegic_migraine": 2,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|not_specified|Familial_hemiplegic_migraine": 1,
    "ATP1A2-related_disorder|Familial_hemiplegic_migraine|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_provided|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_specified|Familial_hemiplegic_migraine": 1,
    "not_provided|ATP1A2-related_disorder|Inborn_genetic_diseases|Familial_hemiplegic_migraine": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine|not_provided": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 4,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Migraine|_familial_hemiplegic|_2|not_provided|Alternating_hemiplegia_of_childhood_1|Familial_hemiplegic_migraine|not_specified": 1,
    "Familial_hemiplegic_migraine|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_98|ATP1A2-related_disorder": 1,
    "Familial_hemiplegic_migraine|Inborn_genetic_diseases|not_provided|not_specified|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 7,
    "not_specified|Developmental_and_epileptic_encephalopathy_98|not_provided|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Familial_hemiplegic_migraine|Alternating_hemiplegia_of_childhood_1|Developmental_and_epileptic_encephalopathy|_1|Migraine|_familial_hemiplegic|_2": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Polymicrogyria|not_provided": 1,
    "Familial_hemiplegic_migraine|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_specified|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_98|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Migraine|_familial_hemiplegic|_2|not_specified|not_provided|Familial_hemiplegic_migraine": 1,
    "Familial_hemiplegic_migraine|not_specified|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|not_provided|Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2": 1,
    "Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Inborn_genetic_diseases|Familial_hemiplegic_migraine|not_specified|not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1": 1,
    "Familial_hemiplegic_migraine|Epilepsy": 1,
    "not_specified|not_provided|Familial_hemiplegic_migraine": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_provided|not_specified|Familial_hemiplegic_migraine": 1,
    "Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_provided|not_specified": 1,
    "Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Developmental_and_epileptic_encephalopathy_98|not_provided|Alternating_hemiplegia_of_childhood_1": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Alternating_hemiplegia_of_childhood_1|Migraine|_familial_hemiplegic|_2|not_provided": 3,
    "Migraine|_familial_hemiplegic|_2|not_provided|Alternating_hemiplegia_of_childhood_1": 1,
    "Migraine|_familial_hemiplegic|_2|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "not_provided|Migraine|_familial_hemiplegic|_2|Developmental_and_epileptic_encephalopathy_98|Alternating_hemiplegia_of_childhood_1|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Alternating_hemiplegia_of_childhood_1|not_provided|Migraine|_familial_hemiplegic|_2|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_1|Developmental_and_epileptic_encephalopathy_98|Migraine|_familial_hemiplegic|_2|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Migraine|_familial_hemiplegic|_2|not_provided|Alternating_hemiplegia_of_childhood_1|Developmental_and_epileptic_encephalopathy_98|Fetal_akinesia|_respiratory_insufficiency|_microcephaly|_polymicrogyria|_and_dysmorphic_facies": 1,
    "Alternating_hemiplegia_of_childhood|Familial_hemiplegic_migraine|not_provided": 1,
    "Migraine|_familial_hemiplegic|_2|Alternating_hemiplegia_of_childhood_1|not_provided": 1,
    "Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload": 9,
    "not_provided|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload": 5,
    "CASQ1-related_disorder|not_provided": 2,
    "not_provided|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|not_provided": 1,
    "Myopathy_with_tubular_aggregates": 4,
    "not_provided|CASQ1-related_disorder": 1,
    "not_specified|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|not_provided": 1,
    "Myopathy_with_tubular_aggregates|not_provided": 1,
    "Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|CASQ1-related_disorder|not_provided": 1,
    "CASQ1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload": 2,
    "not_provided|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|CASQ1-related_disorder": 2,
    "CASQ1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|not_provided|Inborn_genetic_diseases": 1,
    "Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|not_provided": 3,
    "Inborn_genetic_diseases|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload": 1,
    "not_provided|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload|not_specified": 1,
    "Myopathy|not_provided|Myopathy_due_to_calsequestrin_and_SERCA1_protein_overload": 1,
    "Giant_axonal_neuropathy_2": 3,
    "Neurofibromatosis|_type_1|not_specified": 17,
    "DCAF8-related_disorder|not_provided": 2,
    "DCAF8-related_disorder": 2,
    "Giant_axonal_neuropathy_2|not_provided": 1,
    "not_provided|Giant_axonal_neuropathy_2|DCAF8-related_disorder": 1,
    "not_provided|DCAF8-related_disorder": 1,
    "not_specified|Giant_axonal_neuropathy_2": 1,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)": 311,
    "not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 21,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|not_provided": 14,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 9,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_12A_(Zellweger)|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 3,
    "not_provided|PEX19-related_disorder|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|Inborn_genetic_diseases|not_provided": 1,
    "PEX19-related_disorder": 7,
    "PEX19-related_disorder|not_specified|not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|Inborn_genetic_diseases": 6,
    "not_specified|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "PEX19-related_disorder|not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 1,
    "PEX19-related_disorder|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 4,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|not_provided|PEX19-related_disorder": 2,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)|Inborn_genetic_diseases": 1,
    "not_specified|PEX19-related_disorder|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "PEX19-related_disorder|not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_12A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_12A_(Zellweger)|PEX19-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_12A_(Zellweger)|PEX19-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_12A_(Zellweger)|PEX19-related_disorder|not_specified": 1,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 11,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome": 678,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|Inborn_genetic_diseases": 18,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|COPA-related_disorder": 2,
    "not_provided|Autoimmune_interstitial_lung_disease-arthritis_syndrome": 17,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_provided": 18,
    "Inborn_genetic_diseases|Autoimmune_interstitial_lung_disease-arthritis_syndrome": 35,
    "COPA-related_disorder": 6,
    "Systemic_autoinflammation": 1,
    "not_provided|Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_specified": 1,
    "COPA-related_disorder|Autoimmune_interstitial_lung_disease-arthritis_syndrome": 4,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_provided|not_specified": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_provided": 2,
    "not_specified|Autoimmune_interstitial_lung_disease-arthritis_syndrome": 1,
    "not_specified|not_provided|Autoimmune_interstitial_lung_disease-arthritis_syndrome": 3,
    "not_provided|Autoimmune_interstitial_lung_disease-arthritis_syndrome|COPA-related_disorder": 1,
    "COPA-related_disorder|Autoimmune_interstitial_lung_disease-arthritis_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_provided": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|COPA-related_disorder|Inborn_genetic_diseases": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_provided|COPA-related_disorder": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|See_cases|not_provided": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|Systemic_lupus_erythematosus|_susceptibility_to|_1": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_specified": 1,
    "COPA-related_disorder|Autoimmune_interstitial_lung_disease-arthritis_syndrome|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Autoimmune_interstitial_lung_disease-arthritis_syndrome": 1,
    "NCSTN-related_disorder": 3,
    "NCSTN-related_disorder|not_provided": 5,
    "Acne_inversa|_familial|_1|not_provided": 2,
    "not_provided|NCSTN-related_disorder": 4,
    "Acne_inversa|_familial|_1": 12,
    "not_provided|Acne_inversa|_familial|_1": 4,
    "not_provided|Inborn_genetic_diseases|Acne_inversa|_familial|_1": 1,
    "not_provided|NCSTN-related_disorder|Acne_inversa|_familial|_1": 1,
    "Acne_inversa|_familial|_1|NCSTN-related_disorder|not_provided": 1,
    "Abnormality_of_the_skin": 12,
    "VANGL2-related_disorder": 3,
    "not_provided|VANGL2-related_disorder": 2,
    "Inborn_genetic_diseases|Neural_tube_defects|_susceptibility_to": 1,
    "not_provided|Neural_tube_defect": 2,
    "LY9-related_disorder": 1,
    "CD244-related_disorder": 1,
    "not_provided|CD244-related_disorder": 1,
    "Hyperlipidemia|_familial_combined|_susceptibility_to": 2,
    "NECTIN4-related_disorder": 1,
    "Ectodermal_dysplasia-syndactyly_syndrome_1": 11,
    "Ectodermal_dysplasia-syndactyly_syndrome_1|not_provided": 2,
    "not_provided|Ectodermal_dysplasia-syndactyly_syndrome_1|NECTIN4-related_disorder": 1,
    "NECTIN4-related_disorder|not_provided": 1,
    "not_provided|NECTIN4-related_disorder": 1,
    "BRAIN_SMALL_VESSEL_DISEASE_4": 1,
    "BRAIN_SMALL_VESSEL_DISEASE_4|not_specified": 1,
    "Neurodevelopmental_disorder_with_spasticity_and_poor_growth": 9,
    "UFC1-related_disorder": 2,
    "not_specified|UFC1-related_disorder": 1,
    "Variegate_porphyria": 32,
    "not_provided|Variegate_porphyria": 14,
    "Variegate_porphyria|_childhood-onset|Variegate_porphyria": 2,
    "Variegate_porphyria|_childhood-onset|not_provided|Variegate_porphyria": 1,
    "PPOX-related_disorder": 1,
    "Variegate_porphyria|not_provided": 3,
    "Variegate_porphyria|_childhood-onset": 6,
    "not_provided|Variegate_porphyria|See_cases": 1,
    "Acute_intermittent_porphyria|not_provided": 25,
    "PPOX-related_disorder|Variegate_porphyria|_childhood-onset|not_provided|Variegate_porphyria": 1,
    "Inborn_genetic_diseases|not_provided|Variegate_porphyria|_childhood-onset|Variegate_porphyria": 1,
    "PPOX-related_disorder|not_provided": 1,
    "Variegate_porphyria|Variegate_porphyria|_childhood-onset|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Variegate_porphyria": 1,
    "not_provided|Variegate_porphyria|Variegate_porphyria|_childhood-onset": 1,
    "Abnormal_blistering_of_the_skin|Porphyrinuria|Abdominal_colic|not_provided": 1,
    "Abnormal_blistering_of_the_skin|Constipation|Migraine|Abnormal_urinary_color": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1": 219,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_6": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 62,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_provided": 4,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_provided": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_6": 5,
    "not_provided|NDUFS2-related_disorder": 1,
    "NDUFS2-related_disorder": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_provided|not_specified": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 38,
    "NDUFS2-related_disorder|not_provided": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_6|Inborn_genetic_diseases": 1,
    "Leber-like_hereditary_optic_neuropathy|_autosomal_recessive_2|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_specified|not_provided": 1,
    "NDUFS2-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_specified|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_6": 6,
    "Leber_optic_atrophy": 4,
    "Leber-like_hereditary_optic_neuropathy|_autosomal_recessive_2|Mitochondrial_complex_I_deficiency|_nuclear_type_6|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided": 11,
    "not_provided|NDUFS2-related_disorder|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|not_specified": 3,
    "not_specified|Mitochondrial_complex_I_deficiency|not_provided": 1,
    "NDUFS2-related_disorder|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_6": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_6": 1,
    "NDUFS2-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "Leber-like_hereditary_optic_neuropathy|_autosomal_recessive_2": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified": 4,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFS2-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_specified|not_provided": 1,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_6": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 2,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_6|Leber-like_hereditary_optic_neuropathy|_autosomal_recessive_2": 1,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_6": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_6|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|not_provided": 17,
    "NDUFS2-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_6|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Optic_atrophy|NDUFS2-related_disorder|not_specified": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_6|not_specified": 1,
    "not_provided|NDUFS2-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency": 68,
    "not_provided|Mitochondrial_complex_I_deficiency": 24,
    "not_provided|not_specified|APOA2-related_disorder": 1,
    "Apolipoprotein_A-II_deficiency": 3,
    "Apolipoprotein_A-II_deficiency|not_specified": 2,
    "not_provided|Apolipoprotein_A-II_deficiency|APOA2-related_disorder": 1,
    "APOLIPOPROTEIN_A-II_DEFICIENCY|_FAMILIAL|_DUE_TO_APOA-II_(HIROSHIMA)": 1,
    "not_provided|Apolipoprotein_A-II_deficiency|not_specified": 1,
    "not_specified|APOA2-related_disorder": 1,
    "not_provided|not_specified|Apolipoprotein_A-II_deficiency": 1,
    "APOA2-related_disorder|Apolipoprotein_A-II_deficiency|not_specified": 1,
    "APOA2-related_disorder|not_provided|not_specified": 1,
    "APOA2-related_disorder": 1,
    "Apolipoprotein_A-II_amyloidosis|Hypercholesterolemia|_familial|_1": 1,
    "TOMM40L-related_disorder": 1,
    "Kleefstra_syndrome_1": 1429,
    "not_specified|not_provided|NR1I3-related_disorder": 1,
    "NR1I3-related_disorder": 3,
    "NR1I3-related_disorder|not_specified": 1,
    "Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B": 3,
    "Neuropathy|_congenital_hypomyelinating|_2|not_provided|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Roussy-L\u00e9vy_syndrome": 1,
    "Charcot-Marie-Tooth_disease_type_1B|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 2,
    "not_provided|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth|_Intermediate|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Neuropathy|_congenital_hypomyelinating|_2|Roussy-L\u00e9vy_syndrome": 1,
    "Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth|_Intermediate|Charcot-Marie-Tooth_disease|_type_I": 2,
    "not_provided|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B": 3,
    "Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 4,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2": 3,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Roussy-L\u00e9vy_syndrome|not_provided|Neuropathy|_congenital_hypomyelinating|_2": 1,
    "Charcot-Marie-Tooth_disease_type_1B|Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 1,
    "Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_4E|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_type_1B": 1,
    "MPZ-related_disorder|Neuropathy|_congenital_hypomyelinating|_2|not_provided|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B": 1,
    "MPZ-related_disorder": 2,
    "Charcot-Marie-Tooth_disease_type_1B": 13,
    "not_provided|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_D": 8,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2I": 2,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease|_type_I": 2,
    "Dejerine-Sottas_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease|_type_I|Congenital_hypomyelinating_neuropathy|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_type_2I": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 4,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided": 57,
    "Roussy-L\u00e9vy_syndrome|Sensorimotor_neuropathy|EMG:_neuropathic_changes|Limb_muscle_weakness|Tremor": 1,
    "Roussy-L\u00e9vy_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_4E|Neuropathy|_congenital_hypomyelinating|_2|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 37,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Dejerine-Sottas_disease": 23,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_type_I": 32,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 3,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1B": 4,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 25,
    "Charcot-Marie-Tooth_disease|_type_I|not_specified|not_provided": 3,
    "not_specified|Charcot-Marie-Tooth_disease|_type_I": 3,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease": 2,
    "Neuropathy|_congenital_hypomyelinating|_2": 4,
    "Charcot-Marie-Tooth_disease_type_4E|not_specified|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Neuropathy|_congenital_hypomyelinating|_2|Inborn_genetic_diseases|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Neuropathy|_congenital_hypomyelinating|_2|not_provided": 1,
    "Roussy-L\u00e9vy_syndrome": 2,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2|not_specified|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided": 3,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Dejerine-Sottas_disease": 4,
    "Neuropathy|_congenital_hypomyelinating|_2|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease_type_1B|Dejerine-Sottas_disease": 2,
    "Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease": 6,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 23,
    "not_provided|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|not_specified|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_1B|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_2I|DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B": 3,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1B": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Intellectual_disability": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 6,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|not_provided": 3,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_type_1B|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_2I|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "MPZ-related_disorder|not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease|_type_I": 7,
    "Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|MPZ-related_disorder|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease|_type_I|Neuropathy|_congenital_hypomyelinating|_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Dejerine-Sottas_disease|not_provided": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease_type_1B|not_provided|Charcot-Marie-Tooth_disease|_type_I|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B": 5,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease|_type_I": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 12,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_2J|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_1B|Roussy-L\u00e9vy_syndrome": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_1B": 2,
    "Distal_hereditary_motor_neuropathy_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_2I": 1,
    "Dejerine-Sottas_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 4,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_1B": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 7,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2I|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Autosomal_recessive_Dejerine-Sottas_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2J": 2,
    "Charcot-Marie-Tooth_disease|MPZ-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided|MPZ-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Inborn_genetic_diseases|MPZ-related_disorder|Charcot-Marie-Tooth_disease_type_1B|not_provided|Charcot-Marie-Tooth_disease|_type_I|Pes_cavus|Distal_lower_limb_amyotrophy|Decreased_nerve_conduction_velocity|Sensory_neuropathy|Distal_muscle_weakness|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I|not_provided|Neuropathy|_congenital_hypomyelinating|_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_2J|Dejerine-Sottas_disease|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_1B|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_specified": 6,
    "Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Hereditary_motor_neuron_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_2I": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|See_cases": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Dejerine-Sottas_disease|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_1B": 1,
    "CHARCOT-MARIE-TOOTH_DISEASE|_TYPE_1B|_WITH_FOCALLY_FOLDED_MYELIN_SHEATHS|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|MPZ-related_disorder|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2J": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_D|Neuropathy|_congenital_hypomyelinating|_2": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|not_provided": 2,
    "not_specified|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 2,
    "Neuropathy|_congenital_hypomyelinating|_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Roussy-L\u00e9vy_syndrome": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Dejerine-Sottas_disease|DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT|not_provided|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Tip-toe_gait|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease|_type_I|not_provided|Roussy-L\u00e9vy_syndrome": 1,
    "CHARCOT-MARIE-TOOTH_DISEASE|_TYPE_1B|_WITH_FOCALLY_FOLDED_MYELIN_SHEATHS|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Peripheral_neuropathy": 2,
    "Charcot-Marie-Tooth_disease|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "MPZ-related_disorder|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_dominant_intermediate_D": 1,
    "Charcot-Marie-Tooth_disease_type_1B|MPZ-related_disorder|Charcot-Marie-Tooth_disease|_type_I|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease_type_2I": 1,
    "Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_type_1B|Neuropathy|_congenital_hypomyelinating|_2|Dejerine-Sottas_disease|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_1B|Dejerine-Sottas_disease": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|_type_I": 5,
    "Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_dominant_intermediate_D|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|not_specified|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_2I|Charcot-Marie-Tooth_disease_type_2J|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B|Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "not_specified|Roussy-L\u00e9vy_syndrome|Neuropathy|_congenital_hypomyelinating|_2|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease_dominant_intermediate_D|Charcot-Marie-Tooth_disease_type_1B": 1,
    "Charcot-Marie-Tooth|_Intermediate|Hereditary_cancer-predisposing_syndrome|not_provided|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Charcot-Marie-Tooth_disease_type_4E|Hereditary_pheochromocytoma-paraganglioma|Charcot-Marie-Tooth_disease|_type_I|not_specified|Roussy-L\u00e9vy_syndrome|Pheochromocytoma": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Pheochromocytoma|not_specified": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|SDHC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided": 17,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 179,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 62,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 102,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided": 8,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 40,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 34,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome": 31,
    "Carney_triad|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 5,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 2,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|SDHC-related_disorder|Pheochromocytoma/paraganglioma_syndrome_3|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 2,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_provided|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 6,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided": 2,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Pheochromocytoma/paraganglioma_syndrome_3": 40,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3": 3,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 4,
    "Charcot-Marie-Tooth|_Intermediate|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_specified|Hereditary_cancer-predisposing_syndrome|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_4E|Roussy-L\u00e9vy_syndrome|Pheochromocytoma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Pheochromocytoma|not_provided|SDHC-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided": 6,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|SDHC-related_disorder|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 8,
    "not_specified|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 3,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome": 6,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_provided": 4,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|not_provided|SDHC-related_disorder|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided|SDHC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3": 3,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1153,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "SDHC-related_disorder|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_provided|Carney-Stratakis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_specified|SDHC-related_disorder|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Neuroblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_specified": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_pheochromocytoma-paraganglioma": 4,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|SDHC-related_disorder|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney_triad": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|not_specified|not_provided": 1,
    "Cowden_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|SDHC-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|SDHC-related_disorder|Gastrointestinal_stromal_tumor|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Cowden_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|SDHC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|SDHC-related_disorder|not_provided|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|SDHC-related_disorder|Gastrointestinal_stromal_tumor": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Carney_triad|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome": 1,
    "not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|not_specified": 1,
    "SDHC-related_disorder|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Carney-Stratakis_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|SDHC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "SDHC-related_disorder|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor": 1,
    "Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|SDHC-related_disorder|not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHC-related_disorder": 5,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_3|Gastrointestinal_stromal_tumor|Ovarian_cancer|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma|Malignant_tumor_of_breast": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma/paraganglioma_syndrome_3": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_3": 1,
    "SDHC-related_disorder|Hereditary_pheochromocytoma-paraganglioma|not_specified|Carney-Stratakis_syndrome|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Pheochromocytoma|not_provided": 15,
    "FCGR2A-related_disorder": 2,
    "FCGR2A-related_disorder|not_specified|not_provided": 2,
    "Cystic_fibrosis|Systemic_lupus_erythematosus|Malaria|_susceptibility_to": 1,
    "not_specified|not_provided|Lupus_nephritis|_susceptibility_to|Pseudomonas_aeruginosa|_susceptibility_to_chronic_infection_by|_in_cystic_fibrosis|Malaria|_severe|_susceptibility_to": 1,
    "not_provided|Cystic_fibrosis|Systemic_lupus_erythematosus|Malaria|_susceptibility_to": 1,
    "Autosomal_recessive_primary_immunodeficiency_with_defective_spontaneous_natural_killer_cell_cytotoxicity": 4,
    "not_specified|not_provided|Autosomal_recessive_primary_immunodeficiency_with_defective_spontaneous_natural_killer_cell_cytotoxicity": 1,
    "not_specified|Autosomal_recessive_primary_immunodeficiency_with_defective_spontaneous_natural_killer_cell_cytotoxicity": 1,
    "Autosomal_recessive_primary_immunodeficiency_with_defective_spontaneous_natural_killer_cell_cytotoxicity|not_provided": 1,
    "Systemic_lupus_erythematosus|_susceptibility_to": 2,
    "Malaria|_resistance_to|Systemic_lupus_erythematosus|_susceptibility_to": 1,
    "Achromatopsia_7": 16,
    "not_provided|ATF6-related_disorder": 2,
    "Achromatopsia_7|not_provided": 7,
    "ATF6-related_disorder|not_provided": 1,
    "Achromatopsia|not_provided": 34,
    "Achromatopsia_7|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Achromatopsia_7": 1,
    "Retinal_disorders|not_provided": 1,
    "ATF6-related_disorder": 2,
    "ATF6-related_disorder|Achromatopsia_7|not_provided|Bilateral_sensorineural_hearing_impairment": 1,
    "not_provided|Achromatopsia_7": 3,
    "Bilateral_sensorineural_hearing_impairment|Achromatopsia_7": 1,
    "Nephrotic_syndrome|_type_22": 3,
    "not_provided|Nephrotic_syndrome|_type_22|Cardiac_arrhythmia": 1,
    "not_provided|Nephrotic_syndrome|_type_22": 1,
    "NOS1AP-related_disorder|not_provided": 1,
    "NOS1AP-related_disorder": 1,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome": 30,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_provided": 9,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_specified|not_provided|Warburg-cinotti_syndrome": 1,
    "Connective_tissue_disorder|not_provided|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome": 1,
    "DDR2-related_disorder|not_provided": 1,
    "Warburg-cinotti_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome": 15,
    "not_provided|Connective_tissue_disorder|not_specified|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome": 1,
    "not_provided|DDR2-related_disorder": 1,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_provided|DDR2-related_disorder": 1,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome": 1,
    "Connective_tissue_disorder|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_provided|not_specified": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|Connective_tissue_disorder|not_specified": 1,
    "Squamous_cell_lung_carcinoma": 22,
    "not_provided|Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome": 1,
    "DDR2-related_disorder": 5,
    "not_provided|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|Squamous_cell_lung_carcinoma|Warburg-cinotti_syndrome|not_specified": 1,
    "Lung_adenocarcinoma": 102,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|Connective_tissue_disorder|not_provided": 1,
    "not_specified|not_provided|DDR2-related_disorder|Inborn_genetic_diseases": 1,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_specified": 1,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_provided|not_specified|Squamous_cell_lung_carcinoma|Warburg-cinotti_syndrome": 1,
    "Squamous_cell_lung_carcinoma|not_provided": 5,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|Connective_tissue_disorder|not_specified|not_provided": 1,
    "not_provided|DDR2-related_disorder|Warburg-cinotti_syndrome|not_specified": 1,
    "not_provided|Warburg-cinotti_syndrome": 1,
    "Warburg-cinotti_syndrome": 2,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|Squamous_cell_lung_carcinoma|not_specified|Warburg-cinotti_syndrome|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_provided|Connective_tissue_disorder": 1,
    "Fetal_growth_restriction": 1,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|Warburg-cinotti_syndrome|not_provided": 1,
    "Warburg-cinotti_syndrome|not_provided": 1,
    "not_provided|Squamous_cell_lung_carcinoma": 5,
    "not_specified|Spondyloepimetaphyseal_dysplasia-short_limb-abnormal_calcification_syndrome|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia": 2,
    "not_provided|Spondyloepimetaphyseal_dysplasia": 2,
    "not_provided|Short_stature|Microcephaly": 1,
    "4p_partial_monosomy_syndrome": 15,
    "PBX1-related_disorder": 10,
    "Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay|See_cases": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay": 56,
    "PBX1-related_disorder|not_provided": 2,
    "not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay": 6,
    "Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay|not_provided": 6,
    "Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay|Autism_spectrum_disorder": 1,
    "PBX1-related_intellectual_disability_and_pleiotropic_developmental_defects|Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay": 1,
    "coracoclavicular_ankylosis": 2,
    "PBX1-related_disorder|Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay|not_provided": 1,
    "Inborn_genetic_diseases|PBX1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_syndrome_with_or_without_hearing_loss|_abnormal_ears|_or_developmental_delay|PBX1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal-Recessive_Hereditary_Hearing_Impairment|Sensorineural_hearing_loss_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_7|not_provided": 1,
    "not_provided|LMX1A-related_disorder": 2,
    "not_specified|LMX1A-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_7": 13,
    "LMX1A-related_disorder": 10,
    "LMX1A-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_7": 1,
    "LMX1A-related_disorder|not_specified": 1,
    "Monogenic_hearing_loss": 11,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_7": 1,
    "ALDH9A1*2_POLYMORPHISM": 1,
    "Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_1|not_provided": 2,
    "Cerebro-facio-thoracic_dysplasia|not_provided|Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_1": 1,
    "Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_1": 8,
    "not_provided|Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_1": 1,
    "Inborn_genetic_diseases|Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_1|not_provided|TMCO1-related_disorder": 1,
    "Immunodeficiency_25": 123,
    "Immunodeficiency_25|not_specified": 10,
    "not_provided|Immunodeficiency_25": 7,
    "not_provided|CD247-related_disorder|Immunodeficiency_25": 1,
    "not_specified|Immunodeficiency_25": 2,
    "Severe_combined_immunodeficiency_disease|CD247-related_disorder|Immunodeficiency_25|not_provided": 1,
    "not_provided|not_specified|Immunodeficiency_25": 1,
    "Immunodeficiency_25|not_provided|not_specified": 1,
    "Immunodeficiency_25|not_provided": 1,
    "not_specified|Immunodeficiency_25|not_provided": 1,
    "CREG1-related_disorder": 2,
    "not_specified|Familial_idiopathic_hypercalciuria|not_provided": 2,
    "not_provided|Familial_idiopathic_hypercalciuria": 15,
    "Familial_idiopathic_hypercalciuria|not_provided": 10,
    "ADCY10-related_disorder|not_provided": 6,
    "Familial_idiopathic_hypercalciuria|not_provided|not_specified": 1,
    "ADCY10-related_disorder|not_specified": 1,
    "not_provided|ADCY10-related_disorder": 9,
    "not_provided|not_specified|Familial_idiopathic_hypercalciuria": 2,
    "Familial_idiopathic_hypercalciuria": 7,
    "not_provided|Familial_idiopathic_hypercalciuria|not_specified": 3,
    "not_provided|ADCY10-related_disorder|Familial_idiopathic_hypercalciuria": 1,
    "Familial_idiopathic_hypercalciuria|not_provided|ADCY10-related_disorder": 1,
    "not_specified|Familial_idiopathic_hypercalciuria": 1,
    "not_provided|Familial_idiopathic_hypercalciuria|ADCY10-related_disorder": 1,
    "Familial_idiopathic_hypercalciuria|not_specified|not_provided": 3,
    "not_provided|not_specified|ADCY10-related_disorder": 1,
    "not_specified|not_provided|Familial_idiopathic_hypercalciuria": 2,
    "ADCY10-related_disorder": 5,
    "Familial_idiopathic_hypercalciuria|ADCY10-related_disorder|not_provided": 1,
    "not_specified|ADCY10-related_disorder|not_provided": 1,
    "Reduced_sperm_motility|Abnormal_sperm_morphology": 8,
    "ADCY10-related_disorder|Familial_idiopathic_hypercalciuria|not_provided": 1,
    "Familial_idiopathic_hypercalciuria|not_specified": 1,
    "not_provided|ADCY10-related_disorder|not_specified": 1,
    "DCAF6-related_condition|Cerebral_visual_impairment_and_intellectual_disability": 1,
    "Predisposition_to_medulloblastoma": 1,
    "Medulloblastoma|not_provided": 5,
    "GPR161-related_disorder|not_provided": 1,
    "not_provided|not_specified|Medulloblastoma": 1,
    "not_provided|Medulloblastoma": 17,
    "Medulloblastoma|not_specified": 2,
    "not_specified|not_provided|Medulloblastoma": 2,
    "Pituitary_stalk_interruption_syndrome|not_provided|Medulloblastoma": 1,
    "TBX19-related_disorder": 1,
    "not_provided|Congenital_isolated_adrenocorticotropic_hormone_deficiency|TBX19-related_disorder": 1,
    "not_provided|Congenital_isolated_adrenocorticotropic_hormone_deficiency": 18,
    "TBX19-related_disorder|not_specified|not_provided|Congenital_isolated_adrenocorticotropic_hormone_deficiency": 1,
    "Adrenal_insufficiency": 2,
    "not_provided|Congenital_isolated_adrenocorticotropic_hormone_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|TBX19-related_disorder": 1,
    "not_provided|Congenital_isolated_adrenocorticotropic_hormone_deficiency|not_specified": 1,
    "not_provided|not_specified|Congenital_isolated_adrenocorticotropic_hormone_deficiency": 1,
    "Congenital_isolated_adrenocorticotropic_hormone_deficiency|not_provided": 11,
    "Pituitary_stalk_interruption_syndrome": 23,
    "See_cases|Congenital_isolated_adrenocorticotropic_hormone_deficiency": 1,
    "TBX19-related_disorder|not_provided|Congenital_isolated_adrenocorticotropic_hormone_deficiency": 1,
    "TBX19-related_disorder|not_provided": 1,
    "Congenital_isolated_adrenocorticotropic_hormone_deficiency|Inborn_genetic_diseases": 1,
    "Progressive_sensorineural_hearing_impairment": 8,
    "Cardiac_arrhythmia": 907,
    "NME7-related_disorder": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 73,
    "Thiamine-responsive_megaloblastic_anemia|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 11,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided|Thiamine-responsive_megaloblastic_anemia": 4,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Thiamine-responsive_megaloblastic_anemia": 7,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided": 13,
    "not_provided|Thiamine-responsive_megaloblastic_anemia|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 4,
    "not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Thiamine-responsive_megaloblastic_anemia": 2,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided|Inborn_genetic_diseases": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Thiamine-responsive_megaloblastic_anemia": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Inborn_genetic_diseases|not_provided": 2,
    "SLC19A2-related_disorder|not_provided": 2,
    "Monogenic_diabetes|Inborn_genetic_diseases": 2,
    "not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 25,
    "not_specified|SLC19A2-related_disorder|Thiamine-responsive_megaloblastic_anemia|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided": 1,
    "SLC19A2-related_disorder": 2,
    "Inborn_genetic_diseases|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 3,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided|not_specified|Thiamine-responsive_megaloblastic_anemia": 2,
    "Possible_mitochondrial_disorder_-_nuclear_genes": 2,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided|Monogenic_diabetes": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_specified|not_provided|Monogenic_diabetes|Thiamine-responsive_megaloblastic_anemia": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Ear_malformation": 1,
    "not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Inborn_genetic_diseases": 3,
    "Thiamine-responsive_megaloblastic_anemia|not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 2,
    "not_provided|SLC19A2-related_disorder": 1,
    "Thiamine-responsive_megaloblastic_anemia|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_provided": 1,
    "not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Inborn_genetic_diseases|Thiamine-responsive_megaloblastic_anemia|not_specified": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Inborn_genetic_diseases|not_provided|Thiamine-responsive_megaloblastic_anemia": 1,
    "not_provided|Sensorineural_hearing_loss_disorder": 1,
    "Monogenic_diabetes|not_provided|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness": 1,
    "not_specified|Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|Thiamine-responsive_megaloblastic_anemia|not_provided": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_specified|Thiamine-responsive_megaloblastic_anemia": 1,
    "Megaloblastic_anemia|_thiamine-responsive|_with_diabetes_mellitus_and_sensorineural_deafness|not_specified": 1,
    "Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome": 4,
    "Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 34,
    "Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency": 2,
    "Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency|Budd-Chiari_syndrome": 2,
    "Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome|Factor_V_deficiency": 2,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 2,
    "Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 13,
    "Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome": 2,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 3,
    "Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency": 3,
    "Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect": 1,
    "Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance": 3,
    "Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome": 6,
    "Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect": 1,
    "Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|not_specified|not_provided": 1,
    "Congenital_factor_V_deficiency": 533,
    "Congenital_factor_V_deficiency|not_provided": 7,
    "Factor_V_deficiency": 39,
    "F5-related_disorder|Congenital_factor_V_deficiency": 2,
    "Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance": 10,
    "F5-related_disorder": 19,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome|Factor_V_deficiency|Ischemic_stroke|not_provided|F5-related_disorder": 1,
    "Congenital_factor_V_deficiency|Inborn_genetic_diseases": 38,
    "Inborn_genetic_diseases|F5-related_disorder|Congenital_factor_V_deficiency": 1,
    "Budd-Chiari_syndrome|Factor_V_deficiency|not_provided|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|not_specified": 1,
    "Inborn_genetic_diseases|Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_factor_V_deficiency": 27,
    "Congenital_factor_V_deficiency|not_specified|not_provided": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 5,
    "Congenital_factor_V_deficiency|Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|not_provided|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency|Budd-Chiari_syndrome": 2,
    "Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Ischemic_stroke|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1": 3,
    "not_specified|not_provided|Congenital_factor_V_deficiency": 1,
    "Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|Thromboembolism|Factor_V_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 12,
    "F5-related_disorder|Inborn_genetic_diseases|Congenital_factor_V_deficiency": 1,
    "Inborn_genetic_diseases|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome": 1,
    "Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome|Congenital_factor_V_deficiency|Inborn_genetic_diseases|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_1": 6,
    "not_provided|Congenital_factor_V_deficiency": 5,
    "F5-related_disorder|Congenital_factor_V_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|F5-related_disorder": 1,
    "Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Congenital_factor_V_deficiency|Abnormal_bleeding": 1,
    "Cholesteatoma": 6,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 2,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Inborn_genetic_diseases|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 2,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Factor_V_deficiency|Budd-Chiari_syndrome|Ischemic_stroke|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Congenital_factor_V_deficiency|Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect|F5-related_disorder|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "Ischemic_stroke|Congenital_factor_V_deficiency|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance": 3,
    "Congenital_factor_V_deficiency|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect": 1,
    "Factor_V_deficiency|F5-related_disorder|Congenital_factor_V_deficiency|not_provided|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome": 1,
    "not_provided|Thrombophilia_due_to_activated_protein_C_resistance|not_specified|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 6,
    "not_provided|Factor_V_deficiency|Budd-Chiari_syndrome|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Ischemic_stroke|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency": 1,
    "F5-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|not_provided": 1,
    "Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Hemorrhage|Inborn_genetic_diseases|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Ischemic_stroke|F5-related_disorder|Congenital_factor_V_deficiency|not_provided": 1,
    "F5-related_disorder|not_provided|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency|Budd-Chiari_syndrome|Thrombocytopenia|Abnormal_bleeding": 1,
    "Congenital_factor_V_deficiency|not_provided|Factor_V_deficiency": 1,
    "Budd-Chiari_syndrome|Factor_V_deficiency|Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect|not_specified": 1,
    "Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|F5-related_disorder|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_provided|Congenital_factor_V_deficiency|Ischemic_stroke|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome|Pregnancy_loss|_recurrent|_susceptibility_to|_1": 1,
    "Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency": 2,
    "Congenital_factor_V_deficiency|Inborn_genetic_diseases|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome|Factor_V_deficiency|Ischemic_stroke|not_provided|F5-related_disorder": 1,
    "Thromboembolism": 5,
    "Hemorrhage": 6,
    "Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1": 93,
    "Inborn_genetic_diseases|Congenital_factor_V_deficiency|not_provided": 2,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome|Ischemic_stroke|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|F5-related_disorder": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Inborn_genetic_diseases|Factor_V_deficiency|Budd-Chiari_syndrome|Ischemic_stroke|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_thrombin_defect": 1,
    "Congenital_factor_V_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 3,
    "Thrombophilia_due_to_thrombin_defect|not_specified|not_provided|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome": 2,
    "Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|not_provided|Factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "Factor_V_deficiency|not_provided": 1,
    "Congenital_factor_V_deficiency|not_specified|not_provided|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Factor_V_deficiency|Budd-Chiari_syndrome": 2,
    "Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 2,
    "not_specified|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_provided|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome": 1,
    "Budd-Chiari_syndrome|Factor_V_deficiency|not_provided|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_specified": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 2,
    "Factor_V_deficiency|not_provided|Congenital_factor_V_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Congenital_factor_V_deficiency|not_specified|Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Congenital_factor_V_deficiency|Pregnancy_loss|_recurrent|_susceptibility_to|_1": 1,
    "Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect": 1,
    "Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance|Inborn_genetic_diseases|Budd-Chiari_syndrome|Factor_V_deficiency": 1,
    "Thrombus": 10,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Inborn_genetic_diseases|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency|Budd-Chiari_syndrome|Ischemic_stroke|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1": 1,
    "Thrombophilia_due_to_thrombin_defect|F5-related_disorder|Inborn_genetic_diseases|Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Inborn_genetic_diseases|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect": 1,
    "Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome|Congenital_factor_V_deficiency|Inborn_genetic_diseases": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 3,
    "Congenital_factor_V_deficiency|Inborn_genetic_diseases|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome|Factor_V_deficiency|Ischemic_stroke|not_provided": 1,
    "F5-related_disorder|Congenital_factor_V_deficiency|Ischemic_stroke|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_factor_V_deficiency": 2,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "Congenital_factor_V_deficiency|Factor_V_deficiency": 4,
    "Congenital_factor_V_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|not_provided": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 2,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Factor_V_deficiency|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|not_specified|Budd-Chiari_syndrome": 1,
    "not_specified|not_provided|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|not_specified|Congenital_factor_V_deficiency|not_provided": 1,
    "not_specified|not_provided|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "not_specified|not_provided|Factor_V_deficiency|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome": 1,
    "Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect|not_specified|Congenital_factor_V_deficiency|not_provided|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|not_specified|not_provided|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "F5-related_disorder|Congenital_factor_V_deficiency|Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|not_provided|Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency": 1,
    "not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|not_specified|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "not_provided|Congenital_factor_V_deficiency|Inborn_genetic_diseases": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Budd-Chiari_syndrome|Factor_V_deficiency|Ischemic_stroke|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency": 1,
    "Budd-Chiari_syndrome|Factor_V_deficiency|Congenital_factor_V_deficiency|not_provided|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|not_specified": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency|Budd-Chiari_syndrome|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Ischemic_stroke|Congenital_factor_V_deficiency": 1,
    "not_specified|not_provided|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome": 1,
    "Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_activated_protein_C_resistance|Ischemic_stroke|Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_an_impaired_coagulation_process|Inborn_genetic_diseases|not_specified|Factor_V_deficiency|not_provided|Budd-Chiari_syndrome|_susceptibility_to|hormonal_contraceptives_for_systemic_use_response_-_Toxicity": 1,
    "Inborn_genetic_diseases|not_provided|Factor_V_deficiency": 1,
    "not_specified|not_provided|Factor_V_deficiency|Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|F5-related_disorder|Factor_V_deficiency": 1,
    "Congenital_factor_V_deficiency|Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "not_provided|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|not_specified": 1,
    "Thrombophilia_due_to_thrombin_defect|not_specified|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|not_provided|Budd-Chiari_syndrome": 1,
    "Factor_V_deficiency|Congenital_factor_V_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Factor_V_deficiency": 2,
    "Thromboembolism|Deep_venous_thrombosis|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_specified|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|Factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "not_provided|Congenital_factor_V_deficiency|Factor_V_Hong_Kong|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Inborn_genetic_diseases": 1,
    "Thromboembolism|Congenital_factor_V_deficiency|Factor_V_deficiency": 1,
    "Congenital_factor_V_deficiency|F5-related_disorder|Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|not_specified": 1,
    "not_specified|not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency|F5-related_disorder|Congenital_factor_V_deficiency|Budd-Chiari_syndrome": 1,
    "Factor_V_deficiency|F5-related_disorder|Budd-Chiari_syndrome": 1,
    "not_specified|Budd-Chiari_syndrome|not_provided|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome": 3,
    "F5-related_disorder|not_provided|Congenital_factor_V_deficiency|Inborn_genetic_diseases": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|Budd-Chiari_syndrome|Ischemic_stroke|Congenital_factor_V_deficiency|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect": 1,
    "Thrombophilia_due_to_thrombin_defect|Budd-Chiari_syndrome|Factor_V_deficiency|not_provided|Congenital_factor_V_deficiency|not_specified|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_factor_V_deficiency|not_provided|not_specified|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Inborn_genetic_diseases|F5-related_disorder|not_provided": 1,
    "Factor_V_deficiency|not_specified|Congenital_factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|not_provided|Budd-Chiari_syndrome|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "Congenital_factor_V_deficiency|Budd-Chiari_syndrome|Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_1|Thrombophilia_due_to_activated_protein_C_resistance|Inborn_genetic_diseases": 1,
    "not_provided|Thrombophilia_due_to_activated_protein_C_resistance": 1,
    "not_provided|Budd-Chiari_syndrome|Factor_V_deficiency|Thrombophilia_due_to_thrombin_defect|Thrombophilia_due_to_activated_protein_C_resistance|Congenital_factor_V_deficiency|not_specified": 1,
    "Thrombophilia_due_to_activated_protein_C_resistance|Factor_V_deficiency|Budd-Chiari_syndrome|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "SELP-related_disorder": 6,
    "SELP-related_disorder|not_provided|SELECTIN_P_POLYMORPHISM": 1,
    "SELECTIN_P_POLYMORPHISM": 1,
    "Premature_coronary_artery_atherosclerosis": 5,
    "not_provided|Coronary_artery_disorder": 3,
    "IgA_nephropathy|_susceptibility_to": 1,
    "Coronary_artery_disorder": 2,
    "KIFAP3-related_disorder": 7,
    "Geroderma_osteodysplastica": 40,
    "Geroderma_osteodysplastica|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|GORAB-related_disorder": 3,
    "not_provided|Geroderma_osteodysplastica": 10,
    "Inborn_genetic_diseases|not_provided|Geroderma_osteodysplastica": 4,
    "not_specified|not_provided|Geroderma_osteodysplastica": 1,
    "Geroderma_osteodysplastica|not_provided": 22,
    "Geroderma_osteodysplastica|not_provided|not_specified": 2,
    "not_provided|Geroderma_osteodysplastica|Inborn_genetic_diseases": 2,
    "Geroderma_osteodysplastica|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Geroderma_osteodysplastica": 2,
    "GORAB-related_disorder|Geroderma_osteodysplastica|not_provided": 1,
    "Inborn_genetic_diseases|Geroderma_osteodysplastica|not_provided": 2,
    "Geroderma_osteodysplastica|Inborn_genetic_diseases|GORAB-related_disorder|not_provided": 1,
    "GORAB-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Geroderma_osteodysplastica|not_provided": 1,
    "GORAB-related_disorder|not_provided|Geroderma_osteodysplastica": 1,
    "PRRX1-related_disorder": 7,
    "Agnathia-otocephaly_complex": 8,
    "not_provided|PRRX1-related_disorder": 1,
    "not_provided|Trimethylaminuria": 24,
    "Trimethylaminuria": 53,
    "FMO3-related_disorder": 3,
    "Trimethylaminuria|not_provided": 13,
    "not_specified|Trimethylaminuria": 1,
    "not_provided|FMO3-related_disorder|Trimethylaminuria|not_specified": 1,
    "not_provided|Trimethylaminuria|not_specified": 3,
    "not_specified|Trimethylaminuria|not_provided": 4,
    "not_provided|FMO3_activity|_decreased": 1,
    "Trimethylaminuria|FMO3-related_disorder|not_provided": 1,
    "Trimethylaminuria|not_provided|See_cases|not_specified": 1,
    "Trimethylaminuria|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Trimethylaminuria": 3,
    "Trimethylaminuria|not_provided|FMO3-related_disorder": 1,
    "Trimethylaminuria|not_provided|not_specified": 2,
    "Trimethylaminuria|not_specified|not_provided": 1,
    "See_cases|Trimethylaminuria|not_provided": 1,
    "not_provided|FMO3-related_disorder": 1,
    "Trimethylaminuria|FMO3-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Trimethylaminuria": 1,
    "not_provided|FMO3-related_disorder|Trimethylaminuria": 1,
    "Glaucoma_1|_open_angle|_A|Glaucoma": 4,
    "Glaucoma|Glaucoma_1|_open_angle|_A": 3,
    "Glaucoma|not_provided|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_of_childhood": 60,
    "MYOC-related_disorder|not_provided|Open-angle_glaucoma": 1,
    "Open-angle_glaucoma": 78,
    "Glaucoma_1|_open_angle|_E": 41,
    "not_provided|Glaucoma_of_childhood|Glaucoma_1|_open_angle|_A": 2,
    "Glaucoma_of_childhood|Glaucoma_1|_open_angle|_A": 10,
    "Open-angle_glaucoma|Glaucoma": 2,
    "Constitutional_megaloblastic_anemia_with_severe_neurologic_disease|Glaucoma_1|_open_angle|_A|Inborn_genetic_diseases|Open-angle_glaucoma": 1,
    "Glaucoma_1|_open_angle|_A|Open-angle_glaucoma|Glaucoma": 7,
    "MYOC-related_disorder|not_provided|Glaucoma_1|_open_angle|_E|Glaucoma_1|_open_angle|_A": 1,
    "not_provided|Glaucoma_1|_open_angle|_E": 3,
    "Glaucoma_1|_open_angle|_A|Glaucoma_of_childhood": 3,
    "Glaucoma_1|_open_angle|_A|Open-angle_glaucoma": 2,
    "Glaucoma_1|_open_angle|_E|not_provided": 2,
    "Glaucoma_of_childhood|GLAUCOMA_1|_OPEN_ANGLE|_A|_DIGENIC|not_provided": 1,
    "MYOC-related_disorder|not_provided|Glaucoma_of_childhood|not_specified|Glaucoma_1|_open_angle|_A|Glaucoma": 1,
    "not_provided|Glaucoma_1|_open_angle|_A|Glaucoma|Glaucoma_1|_open_angle|_E": 1,
    "Glaucoma_of_childhood|not_provided|Glaucoma_1|_open_angle|_A": 2,
    "Glaucoma_of_childhood|Primary_open_angle_glaucoma": 1,
    "Open-angle_glaucoma|MYOC-related_disorder": 1,
    "Glaucoma_of_childhood|not_provided|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_A": 1,
    "not_provided|Glaucoma_of_childhood|not_specified": 1,
    "Glaucoma_1|_open_angle|_E|Glaucoma|Glaucoma_1|_open_angle|_A|not_specified|not_provided": 1,
    "Glaucoma_1|_open_angle|_A|Open-angle_glaucoma|Glaucoma|not_provided": 1,
    "Glaucoma|not_specified|not_provided|Open-angle_glaucoma|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_of_childhood|not_provided": 1,
    "Glaucoma|Open-angle_glaucoma|Glaucoma_1|_open_angle|_A": 4,
    "not_provided|MYOC-related_disorder|Glaucoma_of_childhood": 1,
    "Glaucoma_1|_open_angle|_A|Glaucoma|Glaucoma_of_childhood|not_provided": 1,
    "Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases": 1,
    "Glaucoma_1|_open_angle|_E|MYOC-related_disorder": 1,
    "Open-angle_glaucoma|Glaucoma_1|_open_angle|_A": 2,
    "Glaucoma_1|_open_angle|_E|Glaucoma_1|_open_angle|_A|MYOC-related_disorder|not_specified|not_provided": 1,
    "Glaucoma_1|_open_angle|_A|Glaucoma|Open-angle_glaucoma": 2,
    "Glaucoma_1|_open_angle|_A|MYOC-related_disorder|Glaucoma_of_childhood|Glaucoma": 2,
    "Glaucoma_of_childhood|Glaucoma|not_specified|not_provided|Glaucoma_1|_open_angle|_A": 2,
    "not_provided|Glaucoma_of_childhood": 3,
    "not_specified|Glaucoma_1|_open_angle|_E": 1,
    "Open-angle_glaucoma|Glaucoma_1|_open_angle|_A|Glaucoma": 3,
    "Glaucoma_1|_open_angle|_A|Open-angle_glaucoma|not_provided|Glaucoma": 1,
    "Glaucoma_1|_open_angle|_A|Glaucoma|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases|not_provided": 1,
    "Glaucoma_1|_open_angle|_E|Glaucoma_1|_open_angle|_A|Glaucoma": 2,
    "Open-angle_glaucoma|Glaucoma|not_provided|Glaucoma_1|_open_angle|_A": 1,
    "Inborn_genetic_diseases|not_provided|Open-angle_glaucoma|Glaucoma|Glaucoma_1|_open_angle|_A": 1,
    "not_provided|Open-angle_glaucoma": 2,
    "Glaucoma_1|_open_angle|_A|Glaucoma_1|_open_angle|_E": 1,
    "not_provided|Glaucoma|Glaucoma_of_childhood|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma|Glaucoma_1|_open_angle|_A|Open-angle_glaucoma|not_specified": 1,
    "not_provided|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_of_childhood|not_provided|MYOC-related_disorder|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_of_childhood|MYOC-related_disorder": 1,
    "Inborn_genetic_diseases|Open-angle_glaucoma|Glaucoma|Glaucoma_1|_open_angle|_A": 1,
    "not_provided|MYOC-related_disorder|Glaucoma_of_childhood|GLAUCOMA_3|_PRIMARY_CONGENITAL|_A|_DIGENIC|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_of_childhood|Glaucoma|not_provided|RECLASSIFIED_-_MYOC_POLYMORPHISM|Glaucoma_1|_open_angle|_A": 1,
    "MYOC-related_disorder": 1,
    "Open-angle_glaucoma|not_specified": 1,
    "Glaucoma|Open-angle_glaucoma|not_provided|Glaucoma_1|_open_angle|_A": 1,
    "Glaucoma_1|_open_angle|_A|MYOC-related_disorder|Open-angle_glaucoma|not_provided|not_specified|Glaucoma": 1,
    "METTL13-related_disorder": 19,
    "Deafness|_autosomal_recessive_26|_modifier_of": 1,
    "DNM3-related_condition": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_16": 11,
    "not_provided|Glycosylphosphatidylinositol_biosynthesis_defect_16": 5,
    "Non-immune_hydrops_fetalis|Glycosylphosphatidylinositol_biosynthesis_defect_16": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_16|not_provided|not_specified": 2,
    "PIGC-related_disorder|not_specified|Glycosylphosphatidylinositol_biosynthesis_defect_16|not_provided": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_16|Global_developmental_delay": 1,
    "SUCO-related_disorder": 7,
    "SUCO-related_disorder|not_provided": 6,
    "not_specified|SUCO-related_disorder|not_provided": 1,
    "not_provided|SUCO-related_disorder": 3,
    "SUCO-related_disorder|not_specified|not_provided": 1,
    "LUNG_CANCER|_SUSCEPTIBILITY_TO": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|not_provided": 16,
    "Autoimmune_lymphoproliferative_syndrome_type_1": 504,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_1|FASLG-related_disorder": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|not_specified": 6,
    "FASLG-related_disorder|not_provided|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "not_specified|Autoimmune_lymphoproliferative_syndrome_type_1": 7,
    "Autoimmune_lymphoproliferative_syndrome_type_1|FASLG-related_disorder": 1,
    "FASLG-related_disorder": 3,
    "FASLG-related_disorder|Autoimmune_lymphoproliferative_syndrome_type_1": 3,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_1": 16,
    "Immunodeficiency_98_with_autoinflammation|_X-linked|not_provided|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IB|not_specified|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IB|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|not_specified|FASLG-related_disorder": 1,
    "Lung_cancer|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|not_specified|not_provided": 2,
    "Autoimmune_lymphoproliferative_syndrome_type_1|Lung_cancer|FASLG-related_disorder": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IB": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|Lung_cancer": 1,
    "KLHL20-related_disorder": 1,
    "Neurodevelopmental_disorder|KLHL20-related_disorder|not_provided|Intellectual_disability|Seizure|See_cases": 1,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 76,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 31,
    "not_specified|not_provided|DARS2-related_disorder|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 1,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_provided": 34,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_disease|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 1,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "Sensorimotor_neuropathy|EMG:_axonal_abnormality|Gout|Clubfoot|Difficulty_walking|Cerebral_cortical_atrophy|Impaired_vibration_sensation_in_the_lower_limbs|Abnormal_foot_morphology|Hypertensive_disorder|CNS_demyelination|not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|Gait_ataxia|Gait_imbalance|Dysmetria": 1,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_specified|not_provided": 3,
    "DARS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|DARS2-related_disorder": 2,
    "not_specified|not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 3,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_specified": 1,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|Mitochondrial_disease|Spastic_ataxia": 1,
    "DARS2-related_disorder|not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|See_cases": 1,
    "Clubfoot|Sensorimotor_neuropathy|EMG:_axonal_abnormality|Gout|Hypertensive_disorder|Cerebral_cortical_atrophy|Impaired_vibration_sensation_in_the_lower_limbs|CNS_demyelination|Difficulty_walking|Abnormal_foot_morphology|Inborn_genetic_diseases|not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|Gait_ataxia|Dysmetria|Gait_imbalance": 1,
    "See_cases|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 1,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_specified|not_provided|DARS2-related_disorder": 1,
    "DARS2-related_disorder|not_specified|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_provided": 1,
    "not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 3,
    "Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_provided|not_specified": 1,
    "DARS2-related_disorder|not_provided": 2,
    "DARS2-related_disorder": 1,
    "Inborn_genetic_diseases|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 2,
    "DARS2-related_disorder|not_specified|not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 1,
    "Inborn_genetic_diseases|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome|not_provided": 1,
    "not_provided|not_specified|DARS2-related_disorder": 1,
    "DARS2-related_disorder|not_provided|Leukoencephalopathy_with_brain_stem_and_spinal_cord_involvement-high_lactate_syndrome": 1,
    "Hereditary_antithrombin_deficiency": 296,
    "SERPINC1-related_disorder": 5,
    "Deep_venous_thrombosis|Hereditary_antithrombin_deficiency": 1,
    "Abnormal_thrombosis|Hereditary_antithrombin_deficiency": 1,
    "Hereditary_antithrombin_deficiency|not_provided": 13,
    "not_provided|Hereditary_antithrombin_deficiency": 12,
    "not_specified|Hereditary_antithrombin_deficiency|Thrombocytopenia|Abnormal_bleeding|not_provided": 1,
    "Tuberous_sclerosis_2": 3960,
    "not_specified|Hereditary_antithrombin_deficiency": 2,
    "Inborn_genetic_diseases|Hereditary_antithrombin_deficiency": 6,
    "Hereditary_antithrombin_deficiency|Inborn_genetic_diseases": 2,
    "Tuberous_sclerosis_2|Hereditary_antithrombin_deficiency": 2,
    "not_specified|Hereditary_antithrombin_deficiency|not_provided": 1,
    "Hereditary_antithrombin_deficiency|SERPINC1-related_disorder": 2,
    "Hereditary_antithrombin_deficiency|not_specified|not_provided": 1,
    "SERPINC1-related_disorder|Hereditary_antithrombin_deficiency": 2,
    "Hereditary_antithrombin_deficiency|Tuberous_sclerosis_2": 1,
    "SERPINC1-related_disorder|Hereditary_antithrombin_deficiency|not_provided": 1,
    "not_provided|Hereditary_antithrombin_deficiency|Deep_venous_thrombosis": 1,
    "not_provided|SERPINC1-related_disorder": 1,
    "not_provided|Hereditary_antithrombin_deficiency|SERPINC1-related_disorder": 1,
    "Deep_venous_thrombosis|not_provided": 1,
    "not_provided|Hereditary_antithrombin_deficiency|Deep_venous_thrombosis|Thromboembolism": 1,
    "See_cases|not_specified": 15,
    "Hemophagocytic_lymphohistiocytosis|_familial|_6": 3,
    "MRPS14-related_disorder|not_provided": 3,
    "Combined_oxidative_phosphorylation_deficiency_38|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_38": 1,
    "MRPS14-related_disorder": 1,
    "Neurodevelopmental_disorder|_nonprogressive|_with_spasticity_and_transient_opisthotonus": 11,
    "Neurodevelopmental_disorder|_nonprogressive|_with_spasticity_and_transient_opisthotonus|Inborn_genetic_diseases": 1,
    "TNR-related_disorder": 3,
    "Neurodevelopmental_disorder|_nonprogressive|_with_spasticity_and_transient_opisthotonus|Non-progressive_neurodevelopmental_disorder_with_spasticity_and_transient_opisthotonus": 8,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|_nonprogressive|_with_spasticity_and_transient_opisthotonus": 2,
    "TNR-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder|_nonprogressive|_with_spasticity_and_transient_opisthotonus": 1,
    "Parkinson_disease|Inborn_genetic_diseases": 2,
    "Parkinson_disease": 7,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 25,
    "not_provided|Parkinson_disease": 1,
    "Inborn_genetic_diseases|not_provided|Parkinson_disease": 1,
    "PAPPA2-related_disorder|not_provided": 1,
    "Short_stature|_Dauber-Argente_type": 5,
    "PAPPA2-related_disorder": 2,
    "ASTN1-related_disorder|not_provided": 1,
    "ASTN1-related_disorder": 1,
    "Abnormal_corpus_callosum_morphology|not_provided": 1,
    "FAM20B-related_condition|not_specified": 1,
    "ABL2-related_condition": 1,
    "Leukemia|_acute_myeloid_with_eosinophilia": 1,
    "Male_infertility|not_specified": 2,
    "not_provided|Nephrotic_syndrome|_type_2": 28,
    "Nephrotic_syndrome|_type_2": 119,
    "Nephrotic_syndrome|_type_2|not_provided": 31,
    "not_provided|not_specified|Nephrotic_syndrome|_type_2": 2,
    "Steroid-resistant_nephrotic_syndrome": 31,
    "Steroid-resistant_nephrotic_syndrome|not_provided": 9,
    "not_provided|Steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_2": 3,
    "not_provided|Steroid-resistant_nephrotic_syndrome|not_specified|Nephrotic_syndrome|_type_2": 3,
    "NPHS2-related_disorder": 2,
    "Nephrotic_syndrome|not_provided|Nephrotic_syndrome|_type_2": 1,
    "Nephrotic_syndrome|_type_2|not_provided|Idiopathic_nephrotic_syndrome": 1,
    "Steroid-resistant_nephrotic_syndrome|not_provided|Nephrotic_syndrome|_type_2": 3,
    "not_provided|Steroid-resistant_nephrotic_syndrome": 6,
    "Focal_segmental_glomerulosclerosis": 59,
    "not_specified|Nephrotic_syndrome|_type_2": 2,
    "Idiopathic_nephrotic_syndrome|Nephrotic_syndrome|_type_2|not_provided": 1,
    "Nephrotic_syndrome|Nephrotic_syndrome|_type_2": 1,
    "Nephrotic_syndrome|_type_2|Kidney_disorder|not_specified|not_provided": 1,
    "not_provided|Idiopathic_nephrotic_syndrome|Nephrotic_syndrome|_type_2|Inborn_genetic_diseases|Nephrotic_syndrome": 1,
    "Steroid-resistant_nephrotic_syndrome|not_provided|NPHS2-related_disorder": 1,
    "not_provided|NPHS2-related_disorder|Steroid-resistant_nephrotic_syndrome": 1,
    "Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|_type_2|not_specified|not_provided": 1,
    "Steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_2|not_provided": 3,
    "Nephrotic_syndrome|_type_2|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_2": 1,
    "NPHS2-related_disorder|not_provided|Nephrotic_syndrome|_type_2|.": 1,
    "NPHS2-related_disorder|not_provided|Nephrotic_syndrome|_type_2|Chronic_kidney_disease|Steroid-resistant_nephrotic_syndrome|Nephrotic_range_proteinuria|Focal_segmental_glomerulosclerosis": 1,
    "Nephrotic_syndrome|_type_2|Idiopathic_nephrotic_syndrome|not_provided": 1,
    "Proteinuria": 2,
    "Steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_2": 2,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_2": 2,
    "NPHS2-related_disorder|Steroid-resistant_nephrotic_syndrome|not_provided|Nephrotic_syndrome|_type_2": 1,
    "not_provided|NPHS2-related_disorder": 3,
    "not_provided|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_2|not_specified": 1,
    "Nephrotic_syndrome|_type_2|not_provided|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome": 1,
    "not_provided|Nephrotic_syndrome|_type_2|Idiopathic_nephrotic_syndrome|Steroid-resistant_nephrotic_syndrome": 1,
    "NPHS2-related_disorder|not_specified|Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|_type_2|not_provided": 1,
    "NPHS2-related_disorder|Proteinuria|Inborn_genetic_diseases|Nephrotic_syndrome|not_specified|not_provided|Nephrotic_syndrome|_type_2|.|Focal_segmental_glomerulosclerosis": 1,
    "Nephrotic_syndrome|_type_2|Steroid-resistant_nephrotic_syndrome": 1,
    "Idiopathic_nephrotic_syndrome": 1,
    "Nephrotic_syndrome|_type_2|Steroid-resistant_nephrotic_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Nephrotic_syndrome|_type_2": 3,
    "Nephrotic_syndrome|_type_2|not_provided|Steroid-resistant_nephrotic_syndrome": 2,
    "Familial_idiopathic_steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_2|Idiopathic_nephrotic_syndrome|NPHS2-related_disorder|Steroid-resistant_nephrotic_syndrome": 1,
    "not_provided|Kidney_disorder": 8,
    "not_provided|Nephrotic_syndrome|_type_2|Idiopathic_nephrotic_syndrome": 1,
    "Nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome|Nephrotic_syndrome|_type_2|Steroid-resistant_nephrotic_syndrome": 1,
    "Steroid-resistant_nephrotic_syndrome|NPHS2-related_disorder|not_provided|Nephrotic_syndrome|_type_2": 1,
    "not_provided|Nephrotic_syndrome|_type_2|not_specified": 2,
    "Prednisolone_response": 38,
    "not_provided|Nephrotic_syndrome|_type_2|not_specified|Kidney_disorder": 1,
    "Nephrotic_syndrome|NPHS2-related_disorder|not_provided|Nephrotic_syndrome|_type_2|Steroid-resistant_nephrotic_syndrome": 1,
    "NPHS2-related_disorder|Nephrotic_syndrome|_type_2|not_specified": 1,
    "NPHS2-related_disorder|Nephrotic_syndrome|not_provided|Nephrotic_syndrome|_type_2|Chronic_kidney_disease|See_cases|Nephrotic_range_proteinuria|Steroid-resistant_nephrotic_syndrome": 1,
    "Idiopathic_nephrotic_syndrome|not_provided|Nephrotic_syndrome|_type_2|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome": 1,
    "Nephrotic_syndrome|Nephrotic_syndrome|_type_2|not_provided": 1,
    "Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Nephrotic_syndrome|_type_2|Proteinuria|not_provided": 1,
    "Corticosteroids_response|not_specified": 1,
    "NPHS2-related_disorder|Nephrotic_syndrome|_type_2|not_provided": 1,
    "Steroid-resistant_nephrotic_syndrome|not_provided|Nephrotic_syndrome|_type_2|not_specified": 1,
    "Steroid-resistant_nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "Nephrotic_syndrome|_type_2|NPHS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Nephrotic_syndrome|_type_2|not_provided": 1,
    "Nephrotic_syndrome|_type_2|Steroid-resistant_nephrotic_syndrome|not_provided": 1,
    "not_provided|Nephrotic_syndrome|_type_2|NPHS2-related_disorder|not_specified|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome": 1,
    "NPHS2-related_disorder|not_specified|not_provided|Finnish_congenital_nephrotic_syndrome|Nephrotic_syndrome|_type_2|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome": 1,
    "Nephrotic_syndrome|_type_2|Nephrotic_syndrome": 1,
    "Focal_segmental_glomerulosclerosis|NPHS2-related_disorder|not_provided|Nephrotic_syndrome|_type_2|not_specified": 1,
    "not_provided|Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|_type_2": 1,
    "not_provided|Nephrotic_syndrome|_type_2|Steroid-resistant_nephrotic_syndrome": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 303,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 17,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 5,
    "Centronuclear_myopathy": 19,
    "TOR1AIP1-related_disorder": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|TOR1AIP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_provided": 18,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|Inborn_genetic_diseases": 13,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 5,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_specified": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|TOR1AIP1-related_disorder": 1,
    "TOR1AIP1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 2,
    "not_provided|TOR1AIP1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|TOR1AIP1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|TOR1AIP1-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Y|not_specified|not_provided": 1,
    "Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 49,
    "not_provided|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 7,
    "LHX4-related_disorder": 5,
    "not_specified|Inborn_genetic_diseases|not_provided|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 1,
    "Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome|not_provided": 4,
    "LHX4-related_disorder|not_provided|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Combined_Pituitary_Hormone_Deficiency|_Dominant": 1,
    "Inborn_genetic_diseases|not_provided|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 1,
    "not_specified|not_provided|LHX4-related_disorder": 1,
    "not_provided|LHX4-related_disorder": 2,
    "Pituitary_hormone_deficiency|_combined|_1": 22,
    "not_specified|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome|not_provided": 2,
    "LHX4-related_disorder|not_provided": 1,
    "Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form": 2,
    "Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_1|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 1,
    "Inborn_genetic_diseases|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 2,
    "Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome|LHX4-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Combined_Pituitary_Hormone_Deficiency|_Dominant": 1,
    "Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome|LHX4-related_disorder|not_provided": 1,
    "LHX4-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome": 2,
    "Short_stature-pituitary_and_cerebellar_defects-small_sella_turcica_syndrome|not_provided|not_specified": 1,
    "ACBD6-related_disorder": 5,
    "not_provided|Neurodevelopmental_disorder_with_progressive_movement_abnormalities": 1,
    "Neurodevelopmental_disorder_with_progressive_movement_abnormalities": 4,
    "Neurodevelopmental_disorder_with_progressive_movement_abnormalities|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_progressive_movement_abnormalities|not_provided": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_6": 6,
    "XPR1-related_disorder|not_provided": 3,
    "Basal_ganglia_calcification|_idiopathic|_6": 8,
    "Basal_ganglia_calcification|_idiopathic|_6|not_provided": 1,
    "not_provided|XPR1-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_6|XPR1-related_primary_familial_brain_calcification": 1,
    "Inborn_genetic_diseases|not_provided|Basal_ganglia_calcification|_idiopathic|_6": 1,
    "XPR1-related_disorder": 1,
    "Inborn_genetic_diseases|Basal_ganglia_calcification|_idiopathic|_6": 1,
    "MR1-related_disorder|not_provided|Immunodeficiency": 1,
    "Developmental_and_epileptic_encephalopathy|_69": 52,
    "Developmental_and_epileptic_encephalopathy|_69|Inborn_genetic_diseases|not_provided": 9,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided": 53,
    "not_provided|CACNA1E-related_disorder": 7,
    "not_provided|Developmental_and_epileptic_encephalopathy|_69|Inborn_genetic_diseases": 8,
    "not_provided|Developmental_and_epileptic_encephalopathy|_69": 66,
    "CACNA1E-related_disorder|not_provided": 8,
    "Developmental_and_epileptic_encephalopathy|_69|CACNA1E-related_disorder|not_provided": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy|_69|CACNA1E-related_disorder": 4,
    "CACNA1E-related_disorder": 9,
    "not_provided|Developmental_and_epileptic_encephalopathy|_69|Developmental_and_epileptic_encephalopathy": 1,
    "CACNA1E-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_69": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_69": 7,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided|CACNA1E-related_disorder": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_69|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided|CACNA1E-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_69": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_69|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_69|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_69|Inborn_genetic_diseases|Van_der_Woude_syndrome_1|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|CACNA1E-related_disorder|Developmental_and_epileptic_encephalopathy|_69": 2,
    "Inborn_genetic_diseases|CACNA1E-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_69": 5,
    "not_provided|CACNA1E-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_69": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_69|CACNA1E-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_69|Intellectual_disability": 1,
    "CACNA1E-related_disorder|Developmental_and_epileptic_encephalopathy|_69|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_69|not_provided|CACNA1E-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_69|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|Episodic_coma": 1,
    "Inborn_genetic_diseases|See_cases|not_provided": 9,
    "Inborn_genetic_diseases|not_provided|CACNA1E-related_disorder": 1,
    "CACNA1E-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_69": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_69|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_69|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_69|Inborn_genetic_diseases|CACNA1E-related_disorder": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|Genetic_developmental_and_epileptic_encephalopathy": 1,
    "not_provided|CACNA1E-related_disorder|Developmental_and_epileptic_encephalopathy|_69|Inborn_genetic_diseases": 1,
    "CACNA1E-related_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_69": 1,
    "Wolff-Parkinson-White_pattern|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_69|not_provided": 1,
    "Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency": 183,
    "not_provided|Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency": 22,
    "Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency|not_provided": 6,
    "Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "GLUL-related_disorder": 5,
    "not_specified|Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency": 2,
    "Inborn_genetic_diseases|Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency": 2,
    "Developmental_and_epileptic_encephalopathy_116": 4,
    "GLUL-related_disorder|not_provided|Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency": 1,
    "Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency|Inborn_genetic_diseases": 1,
    "Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency|GLUL-related_disorder": 1,
    "Inborn_genetic_diseases|GLUL-related_disorder": 1,
    "Congenital_brain_dysgenesis_due_to_glutamine_synthetase_deficiency|not_provided|GLUL-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_116|Glutamine_synthetase_stabilization_disorder|GLUL-related_disorder|Glutamine_related_condition|not_provided": 1,
    "Glutamine_synthetase_stabilization_disorder|Developmental_and_epileptic_encephalopathy|_16|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_16|Developmental_and_epileptic_encephalopathy_116|Glutamine_synthetase_stabilization_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_16|Glutamine_synthetase_stabilization_disorder": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy_116|Developmental_and_epileptic_encephalopathy|_16|Glutamine_synthetase_stabilization_disorder": 1,
    "RNASEL-related_disorder": 6,
    "Hereditary_cancer|Prostate_cancer|_hereditary|_1|Prostate_cancer_susceptibility": 1,
    "RNASEL-related_disorder|not_provided": 1,
    "RNASEL-related_disorder|not_provided|Prostate_cancer|_hereditary|_1|Prostate_cancer": 1,
    "NPL-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_75": 3,
    "Intellectual_developmental_disorder|_autosomal_dominant_75|DHX9-related_disorder": 2,
    "DHX9-associated_neurodevelopmental_disorder": 1,
    "DHX9-related_neurodevelopmental_disorder": 1,
    "LAMC1-related_disorder": 20,
    "LAMC1-related_disorder|not_provided": 4,
    "LAMC1-associated_syndrome": 1,
    "not_provided|LAMC1-related_disorder": 2,
    "LAMC1-related_autism_spectrum_disorder": 1,
    "Junctional_epidermolysis_bullosa": 139,
    "not_provided|Junctional_epidermolysis_bullosa": 30,
    "Junctional_epidermolysis_bullosa|not_provided": 63,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 2,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 241,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|LAMC2-related_disorder": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 27,
    "not_provided|Epidermolysis_bullosa|_junctional_3B|_severe": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Epidermolysis_bullosa|_junctional_3B|_severe|Epidermolysis_bullosa|_junctional_3A|_intermediate|LAMC2-related_disorder": 1,
    "not_provided|Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 2,
    "Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|not_specified": 1,
    "Epidermolysis_bullosa|_junctional_3B|_severe|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Epidermolysis_bullosa|_junctional_3B|_severe|Epidermolysis_bullosa|_junctional_3A|_intermediate": 17,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 2,
    "not_provided|Epidermolysis_bullosa|_junctional_3A|_intermediate": 2,
    "not_provided|LAMC2-related_disorder|Junctional_epidermolysis_bullosa": 5,
    "not_provided|LAMC2-related_disorder|Amelogenesis_imperfecta_type_1|Junctional_epidermolysis_bullosa|not_specified": 1,
    "Junctional_epidermolysis_bullosa|LAMC2-related_disorder|not_specified": 1,
    "not_provided|Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "LAMC2-related_disorder|Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa": 19,
    "LAMC2-related_disorder|Junctional_epidermolysis_bullosa|not_provided": 4,
    "not_provided|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe": 2,
    "not_provided|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "not_provided|Junctional_epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_3A|_intermediate": 1,
    "not_specified|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 35,
    "Junctional_epidermolysis_bullosa|not_specified|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Junctional_epidermolysis_bullosa|not_provided|LAMC2-related_disorder": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|LAMC2-related_disorder|Junctional_epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe": 1,
    "Epidermolysis_bullosa|_junctional_3B|_severe|Epidermolysis_bullosa|_junctional_3A|_intermediate|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 3,
    "LAMC2-related_disorder|not_provided": 3,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type": 75,
    "Epidermolysis_bullosa|_junctional_3B|_severe|Epidermolysis_bullosa|_junctional_3A|_intermediate|Junctional_epidermolysis_bullosa|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3B|_severe": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa|LAMC2-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_3B|_severe": 5,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe": 1,
    "not_provided|LAMC2-related_disorder": 3,
    "not_provided|Junctional_epidermolysis_bullosa|Inborn_genetic_diseases": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|LAMC2-related_disorder|Junctional_epidermolysis_bullosa|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|not_provided": 2,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 30,
    "not_provided|Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3B|_severe|Epidermolysis_bullosa|_junctional_3A|_intermediate": 1,
    "Epidermolysis_bullosa|_junctional_3A|_intermediate": 3,
    "LAMC2-related_disorder|Junctional_epidermolysis_bullosa|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3B|_severe|Epidermolysis_bullosa|_junctional_3A|_intermediate|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa|not_specified": 4,
    "Junctional_epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 3,
    "Junctional_epidermolysis_bullosa|Inborn_genetic_diseases": 5,
    "Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|LAMC2-related_disorder|Junctional_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_3A|_intermediate": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa|not_specified": 1,
    "Junctional_epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_3A|_intermediate|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa|not_specified|not_provided": 3,
    "not_provided|Epidermolysis_bullosa|_junctional_3B|_severe|Abnormality_of_the_skin": 1,
    "not_provided|not_specified|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_3B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|not_provided": 3,
    "Chronic_granulomatous_disease": 53,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_provided": 10,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 478,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "Inborn_genetic_diseases|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 13,
    "NCF2-related_disorder|not_specified|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 3,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_provided|not_specified|NCF2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_28|not_specified|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 18,
    "NCF2-related_disorder|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "not_specified|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|Chronic_granulomatous_disease": 5,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_specified|not_provided": 2,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_provided": 4,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_provided|Chronic_granulomatous_disease": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|NCF2-related_disorder": 3,
    "NCF2-related_disorder": 2,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|NCF2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "NCF2-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 3,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_provided|not_specified": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_2|not_specified": 1,
    "not_provided|Chronic_granulomatous_disease": 1,
    "Immunodeficiency_113_with_autoimmunity_and_autoinflammation": 2,
    "TSEN15-related_disorder": 3,
    "Pontocerebellar_hypoplasia|_type_2F": 3,
    "Global_developmental_delay|Seizure|Primary_microcephaly|Pontocerebellar_hypoplasia|_type_2F": 1,
    "Inborn_genetic_diseases|Short_stature": 1,
    "Congenital_disorder_of_glycosylation|_type_2v": 16,
    "EDEM3-related_disorder": 3,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|_type_2v": 1,
    "Inborn_genetic_diseases|EDEM3-related_disorder": 1,
    "RNF2-associated_neurodevelopmental_condition|Luo-Schoch-Yamamoto_syndrome": 1,
    "Luo-Schoch-Yamamoto_syndrome": 8,
    "RNF2-related_disorder": 2,
    "Immunodeficiency_70": 7,
    "IVNS1ABP-related_disorder": 10,
    "not_specified|Immunodeficiency_70": 1,
    "Age_related_macular_degeneration_1": 91,
    "Macular_degeneration": 18,
    "HMCN1-related_disorder": 10,
    "HMCN1-related_disorder|not_provided|Age_related_macular_degeneration_1": 3,
    "not_provided|Age_related_macular_degeneration_1": 100,
    "Age_related_macular_degeneration_1|not_provided": 103,
    "not_specified|not_provided|Age_related_macular_degeneration_1": 38,
    "HMCN1-related_disorder|not_provided": 17,
    "not_provided|HMCN1-related_disorder|not_specified": 2,
    "not_provided|Age_related_macular_degeneration_1|not_specified": 25,
    "not_provided|not_specified|Age_related_macular_degeneration_1": 13,
    "Age_related_macular_degeneration_1|not_provided|not_specified": 26,
    "Age_related_macular_degeneration_1|not_specified|not_provided": 25,
    "not_provided|Age_related_macular_degeneration_1|HMCN1-related_disorder": 6,
    "not_specified|Age_related_macular_degeneration_1|not_provided": 15,
    "not_provided|HMCN1-related_disorder": 20,
    "HMCN1-related_disorder|not_specified|not_provided": 2,
    "Macular_degeneration|not_provided": 14,
    "Age_related_macular_degeneration_1|HMCN1-related_disorder|not_provided": 5,
    "not_specified|not_provided|HMCN1-related_disorder": 2,
    "Age_related_macular_degeneration_1|not_provided|HMCN1-related_disorder": 4,
    "HMCN1-related_disorder|Age_related_macular_degeneration_1|not_provided": 6,
    "not_provided|HMCN1-related_disorder|Age_related_macular_degeneration_1": 4,
    "Age_related_macular_degeneration_1|not_provided|Macular_degeneration": 2,
    "not_specified|Age_related_macular_degeneration_1": 4,
    "Age_related_macular_degeneration_1|Macular_degeneration|not_specified|not_provided": 1,
    "Age_related_macular_degeneration_1|not_specified": 1,
    "not_specified|HMCN1-related_disorder|not_provided": 1,
    "HMCN1-related_disorder|not_provided|Age_related_macular_degeneration_1|not_specified": 1,
    "Age_related_macular_degeneration_1|not_provided|HMCN1-related_disorder|not_specified": 1,
    "not_specified|HMCN1-related_disorder|not_provided|Age_related_macular_degeneration_1": 1,
    "not_provided|Macular_degeneration": 4,
    "Age_related_macular_degeneration_1|Macular_degeneration|not_provided": 2,
    "MACULAR_DEGENERATION|_AGE-RELATED|_1|_SUSCEPTIBILITY_TO|not_provided|Age_related_macular_degeneration_1": 1,
    "not_provided|Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome": 6,
    "PRG4-related_disorder": 14,
    "Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome": 33,
    "PRG4-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome": 1,
    "not_provided|PRG4-related_disorder": 2,
    "Abnormality_of_the_skeletal_system": 7,
    "not_provided|Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome|not_specified": 1,
    "Camptodactyly-arthropathy-coxa_vara-pericarditis_syndrome|not_provided": 1,
    "PRG4-related_disorder|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "PRG4-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_79": 2,
    "Cholangiocarcinoma": 4,
    "PLA2G4A-related_disorder": 3,
    "Cytosolic_phospholipase-A2_alpha_deficiency_associated_bleeding_disorder": 6,
    "not_provided|PLA2G4A-related_disorder": 2,
    "PLA2G4A-related_disorder|not_provided": 2,
    "Cytosolic_phospholipase-A2_alpha_deficiency_associated_bleeding_disorder|not_provided": 1,
    "RGS2-related_disorder": 1,
    "Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hyperparathyroidism_1": 8,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors": 33,
    "Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 26,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 11,
    "Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma": 20,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|CDC73-related_disorder|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Isolated_Hyperparathyroidism": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 148,
    "Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism|Hyperparathyroidism_2_with_jaw_tumors|not_specified": 1,
    "Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|not_specified|not_provided|Hyperparathyroidism_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 6,
    "Parathyroid_carcinoma": 712,
    "Hyperparathyroidism_2_with_jaw_tumors": 6,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 1,
    "Ossifying_fibroma_of_the_jaw": 2,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma": 207,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 186,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_1": 5,
    "Cystic_parathyroid_adenoma": 1,
    "Hyperparathyroidism_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|_type_1": 1116,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|not_provided": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma": 5,
    "Parathyroid_carcinoma|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|Parathyroid_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Parathyroid_adenoma|_somatic|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|not_provided": 1,
    "not_provided|Parathyroid_carcinoma": 3,
    "Hyperparathyroidism_1": 7,
    "Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Parathyroid_carcinoma": 4,
    "Hyperparathyroidism_1|Parathyroid_carcinoma": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "not_provided|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Familial_cancer_of_breast|Hyperparathyroidism_2_with_jaw_tumors|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1": 2,
    "not_specified|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors": 6,
    "Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hereditary_cancer-predisposing_syndrome": 4,
    "Parathyroid_carcinoma|CDC73-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors": 4,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma": 1,
    "Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Parathyroid_carcinoma|Hyperparathyroidism_1": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|not_provided": 1,
    "Parathyroid_carcinoma|not_specified": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 2,
    "not_specified|Parathyroid_carcinoma": 2,
    "Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hyperparathyroidism_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "CDC73-related_disorder": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|CDC73-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma": 1,
    "Parathyroid_gland_adenoma|Parathyroid_carcinoma": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hyperparathyroidism_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 3,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "CDC73-related_disorder|Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|CDC73-related_disorder": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Parathyroid_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|not_provided": 1,
    "CDC73-related_disorder|Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|not_specified|Hereditary_cancer-predisposing_syndrome|CDC73-related_disorder": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Hyperparathyroidism_1": 1,
    "Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|CDC73-related_disorder|not_provided": 1,
    "Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "CDC73-related_disorder|Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|Parathyroid_carcinoma|not_provided": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|not_provided|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma": 1,
    "not_specified|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|Parathyroid_carcinoma": 1,
    "CDC73-related_disorder|Parathyroid_carcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 2,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hyperparathyroidism_1|Parathyroid_carcinoma|not_provided": 1,
    "Parathyroid_carcinoma|not_specified|Hyperparathyroidism_1|not_provided|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Parathyroid_carcinoma|CDC73-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1|Parathyroid_carcinoma|not_provided|not_specified|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Hereditary_cancer-predisposing_syndrome|CDC73-related_disorder|Parathyroid_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1": 1,
    "Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors|not_provided": 1,
    "Parathyroid_carcinoma|not_provided|not_specified|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Parathyroid_carcinoma|CDC73-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Parathyroid_carcinoma|CDC73-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hyperparathyroidism_1|not_provided": 1,
    "Parathyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|CDC73-related_disorder": 1,
    "Parathyroid_carcinoma|not_provided|Hyperparathyroidism_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma|Hyperparathyroidism_1": 1,
    "Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1|Parathyroid_carcinoma": 7,
    "Isolated_Hyperparathyroidism|Hyperparathyroidism_2_with_jaw_tumors|Parathyroid_carcinoma": 3,
    "Isolated_Hyperparathyroidism|not_provided|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "Isolated_Hyperparathyroidism|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 3,
    "not_provided|Parathyroid_carcinoma|Hyperparathyroidism_1|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "not_provided|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors|Hyperparathyroidism_1": 1,
    "not_provided|Hyperparathyroidism_1|Parathyroid_carcinoma|Hyperparathyroidism_2_with_jaw_tumors": 1,
    "KCNT2-related_disorder": 12,
    "Developmental_and_epileptic_encephalopathy|_57": 35,
    "Neurodevelopmental_delay|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_57|not_provided": 1,
    "not_provided|KCNT2-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_57": 2,
    "KCNT2-related_disorder|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_57|Inborn_genetic_diseases": 2,
    "KCNT2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|_57": 2,
    "KCNT2-related_disorder|Developmental_and_epileptic_encephalopathy|_57|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_57|KCNT2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_57|Inborn_genetic_diseases|not_provided": 1,
    "Mild_global_developmental_delay": 2,
    "CFH-related_disorder|not_provided": 4,
    "CFH-related_disorder": 2,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 9,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 5,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 3,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|not_provided": 1,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 60,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided": 7,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome": 161,
    "not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_4|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen": 2,
    "Age_related_macular_degeneration_4": 3,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided": 1,
    "Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided|Age_related_macular_degeneration_4": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 4,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 44,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 2,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|not_provided": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|not_provided": 2,
    "Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Age_related_macular_degeneration_4|not_provided": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided|not_specified": 1,
    "Focal_segmental_glomerulosclerosis|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided": 1,
    "not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|CFH-related_disorder": 1,
    "not_provided|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen": 1,
    "not_provided|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4": 1,
    "not_provided|Age_related_macular_degeneration_4|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 3,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_specified|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Basal_laminar_drusen": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|not_provided": 2,
    "Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 2,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|not_provided|not_specified": 1,
    "not_specified|Age_related_macular_degeneration_4|not_provided|Atypical_hemolytic-uremic_syndrome|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "not_provided|Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 5,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|not_provided": 2,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|CFH-related_disorder|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|not_provided": 5,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Inborn_genetic_diseases|not_provided": 1,
    "Basal_laminar_drusen": 3,
    "Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided|CFH-related_disorder|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Age_related_macular_degeneration_4|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen": 1,
    "Factor_H_deficiency": 12,
    "Factor_H_deficiency|Basal_laminar_drusen|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4": 1,
    "not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 2,
    "not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency": 1,
    "not_specified|not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Macular_degeneration|Atypical_hemolytic-uremic_syndrome|Basal_laminar_drusen|Mesangiocapillary_glomerulonephritis|_type_II": 1,
    "Basal_laminar_drusen|Age_related_macular_degeneration_4|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 4,
    "Age_related_macular_degeneration_4|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency": 1,
    "not_provided|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Retinal_dystrophy": 1,
    "not_provided|Age_related_macular_degeneration_4": 1,
    "Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided": 3,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|Age_related_macular_degeneration_4|not_provided": 4,
    "not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|CFH-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided|Age_related_macular_degeneration_4": 1,
    "not_provided|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 2,
    "Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 1,
    "Factor_H_deficiency|not_provided": 1,
    "Basal_laminar_drusen|Factor_H_deficiency|Age_related_macular_degeneration_4|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Factor_H_deficiency|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Focal_segmental_glomerulosclerosis|not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4": 1,
    "Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 3,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4": 2,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 3,
    "not_provided|Basal_laminar_drusen|Age_related_macular_degeneration_4|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 4,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|not_provided|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 23,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided|not_specified": 1,
    "Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Age_related_macular_degeneration_4|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Basal_laminar_drusen|Age_related_macular_degeneration_4": 1,
    "not_provided|Age_related_macular_degeneration_4|Atypical_hemolytic-uremic_syndrome|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Hereditary_hemolytic_uremic_syndrome": 1,
    "Kidney_disorder": 52,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency": 2,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 2,
    "not_provided|CFH-related_disorder": 1,
    "Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|not_provided": 2,
    "Basal_laminar_drusen|Age_related_macular_degeneration_4|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "CFH-related_disorder|not_provided|not_specified": 1,
    "Basal_laminar_drusen|Factor_H_deficiency|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 1,
    "Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 2,
    "not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Kidney_disorder": 1,
    "Factor_H_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|not_provided": 2,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 3,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|Age_related_macular_degeneration_4|not_provided|CFH-related_disorder": 1,
    "Age_related_macular_degeneration_4|not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 2,
    "Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Basal_laminar_drusen|not_provided": 2,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|not_provided|Age_related_macular_degeneration_4": 2,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "not_specified|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|not_provided|Age_related_macular_degeneration_4": 1,
    "Factor_H_deficiency|not_provided|Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|not_provided|Age_related_macular_degeneration_4|Inborn_genetic_diseases": 1,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|not_specified|not_provided": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided": 1,
    "Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|not_provided|not_specified": 1,
    "not_specified|Factor_H_deficiency|Focal_segmental_glomerulosclerosis|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Age_related_macular_degeneration_4|Factor_H_deficiency|Basal_laminar_drusen|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-related_disorder": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 1,
    "not_provided|Factor_H_deficiency": 2,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|not_specified|not_provided": 1,
    "Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_specified": 1,
    "CFH-related_disorder|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|not_provided": 1,
    "not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_provided|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4": 1,
    "Age_related_macular_degeneration_4|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 1,
    "not_provided|not_specified|CFH-related_disorder": 1,
    "CFH-related_disorder|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Age_related_macular_degeneration_4|Inborn_genetic_diseases": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Age_related_macular_degeneration_4|not_provided": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|not_provided|Age_related_macular_degeneration_4|not_specified": 1,
    "not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Retinal_dystrophy|Age_related_macular_degeneration_4": 1,
    "Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Factor_H_deficiency|not_provided|Chronic_kidney_disease": 1,
    "Inborn_genetic_diseases|Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Inborn_genetic_diseases|Basal_laminar_drusen|Factor_H_deficiency|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided": 1,
    "not_specified|not_provided|Age_related_macular_degeneration_4|Atypical_hemolytic-uremic_syndrome|Basal_laminar_drusen|Factor_H_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Inborn_genetic_diseases|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Factor_H_deficiency|Age_related_macular_degeneration_4|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Thrombotic_microangiopathy|Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency": 1,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|Age_related_macular_degeneration_4|Factor_H_deficiency": 1,
    "not_provided|Age_related_macular_degeneration_4|Atypical_hemolytic-uremic_syndrome|not_specified|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Focal_segmental_glomerulosclerosis|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency": 1,
    "Atypical_hemolytic-uremic_syndrome|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_specified|not_provided|Age_related_macular_degeneration_4": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|CFH-related_disorder|not_provided|not_specified": 1,
    "Non-immunoglobulin-mediated_membranoproliferative_glomerulonephritis|CFH-related_disorder|not_specified|not_provided|Age_related_macular_degeneration_4|Atypical_hemolytic-uremic_syndrome|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Inborn_genetic_diseases|not_provided|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen": 1,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-related_disorder|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Retinal_dystrophy": 1,
    "not_provided|Factor_H_deficiency|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Kidney_disorder": 1,
    "Factor_H_deficiency|Age_related_macular_degeneration_4|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-related_disorder|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_specified": 1,
    "not_specified|Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen|not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-related_disorder|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Inborn_genetic_diseases|not_provided|Age_related_macular_degeneration_4": 1,
    "CFH-related_disorder|Optic_atrophy|not_provided|not_specified|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Basal_laminar_drusen|Age_related_macular_degeneration_4|Factor_H_deficiency": 1,
    "not_provided|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|Atypical_hemolytic-uremic_syndrome|not_specified|CFH-related_disorder|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_specified|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "not_provided|not_specified|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Kidney_disorder|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency": 1,
    "not_specified|Thrombotic_microangiopathy|Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 1,
    "not_specified|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Kidney_disorder|Age_related_macular_degeneration_4|not_provided": 1,
    "Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_specified": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided|Factor_H_deficiency": 1,
    "Inborn_genetic_diseases|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Basal_laminar_drusen|Age_related_macular_degeneration_4|not_provided|Atypical_hemolytic-uremic_syndrome|not_specified": 1,
    "Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Inborn_genetic_diseases|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_specified|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Inborn_genetic_diseases|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_4|Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 1,
    "Basal_laminar_drusen|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|not_provided": 3,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Age_related_macular_degeneration_4|Basal_laminar_drusen": 1,
    "not_provided|Basal_laminar_drusen|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 1,
    "Retinal_dystrophy|Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Kidney_disorder": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome": 23,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided|Familial_Atypical_Hemolytic-Uremic_Syndrome": 1,
    "Age_related_macular_degeneration_4|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|CFH-related_disorder|not_provided": 1,
    "Factor_H_deficiency|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_specified|not_provided|Age_related_macular_degeneration_4": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|not_provided|Basal_laminar_drusen|Age_related_macular_degeneration_4": 1,
    "Kidney_disorder|Age_related_macular_degeneration_4|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency|Basal_laminar_drusen|Retinal_dystrophy|not_provided|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Atypical_hemolytic-uremic_syndrome": 2,
    "Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_4|Factor_H_deficiency": 1,
    "not_provided|Age_related_macular_degeneration_4|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Factor_H_deficiency|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Basal_laminar_drusen|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "Age_related_macular_degeneration_4|not_provided|Basal_laminar_drusen|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Factor_H_deficiency": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "CFHR3-related_disorder": 2,
    "Age_related_macular_degeneration_1|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 2,
    "not_provided|Age_related_macular_degeneration_1|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Kidney_disorder": 1,
    "not_provided|Age_related_macular_degeneration_1|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 3,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_1|not_provided": 1,
    "Age_related_macular_degeneration_1|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Age_related_macular_degeneration_1|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|not_provided": 1,
    "Cerebral_amyloid_angiopathy|_APP-related": 5,
    "not_specified|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1": 1,
    "not_provided|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_1|Age_related_macular_degeneration_1": 1,
    "Chronic_kidney_disease": 4,
    "not_specified|not_provided|Chronic_kidney_disease": 1,
    "Chronic_kidney_disease|not_specified": 2,
    "not_provided|Kidney_disorder|not_specified": 3,
    "Kidney_disorder|not_specified": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|not_provided": 3,
    "Kidney_disorder|not_provided": 10,
    "Non-immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_provided": 1,
    "Mesangiocapillary_glomerulonephritis|_type_II": 2,
    "CFHR5_deficiency|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Atypical_hemolytic-uremic_syndrome": 1,
    "C3_glomerulonephritis|CFHR5_deficiency": 2,
    "C3_glomerulonephritis": 92,
    "CFHR5_deficiency": 3,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 23,
    "CFHR5_deficiency|not_provided": 5,
    "C3_glomerulonephritis|not_provided": 10,
    "C3_glomerulonephritis|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "Inborn_genetic_diseases|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_provided|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Atypical_hemolytic-uremic_syndrome": 1,
    "C3_glomerulonephritis|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Inborn_genetic_diseases": 1,
    "CFHR5_deficiency|C3_glomerulonephritis|Inborn_genetic_diseases|not_provided": 1,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|CFHR5_deficiency|not_provided": 2,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|C3_glomerulonephritis": 2,
    "not_provided|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 2,
    "CFHR5_deficiency|Kidney_disorder|not_specified|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided": 1,
    "not_provided|Variant_of_unknown_significance": 3,
    "not_provided|Atypical_hemolytic-uremic_syndrome|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided": 1,
    "Inborn_genetic_diseases|C3_glomerulonephritis": 7,
    "C3_glomerulonephritis|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|C3_glomerulonephritis": 1,
    "not_provided|CFHR5_deficiency": 2,
    "not_provided|Kidney_disorder|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_specified": 1,
    "CFHR5_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided|not_specified": 1,
    "Kidney_disorder|not_provided|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_specified|CFHR5_deficiency|not_provided": 1,
    "C3_glomerulonephritis|not_specified|not_provided|CFHR5_deficiency|Chronic_kidney_disease": 1,
    "Kidney_disorder|not_specified|not_provided|Mesangiocapillary_glomerulonephritis|_type_II|CFHR5_deficiency": 1,
    "not_specified|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided": 1,
    "CFHR5_deficiency|not_provided|not_specified": 1,
    "not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 9,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Variant_of_unknown_significance|not_provided|CFHR5_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|C3_glomerulonephritis": 1,
    "not_provided|C3_glomerulonephritis": 14,
    "CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "CFHR5_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Chronic_kidney_disease": 1,
    "CFHR5_deficiency|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Inborn_genetic_diseases": 1,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided": 1,
    "CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Atypical_hemolytic-uremic_syndrome": 1,
    "C3_glomerulonephritis|Inborn_genetic_diseases|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_provided|CFHR5_deficiency|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|C3_glomerulonephritis": 1,
    "not_provided|CFHR5_deficiency|Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_specified|not_provided|CFHR5_deficiency|Inborn_genetic_diseases": 1,
    "CFHR5_deficiency|not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_specified|Atypical_hemolytic-uremic_syndrome": 1,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|CFHR5_deficiency|C3_glomerulonephritis|not_provided|Inborn_genetic_diseases": 1,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|C3_glomerulonephritis|CFHR5_deficiency|not_provided": 1,
    "C3_glomerulonephritis|CFHR5_deficiency|not_provided": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II": 1,
    "not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_specified": 1,
    "CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_provided|CFHR5_deficiency": 1,
    "Atypical_hemolytic-uremic_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|C3_glomerulonephritis|CFHR5_deficiency": 1,
    "Variant_of_unknown_significance|not_provided": 2,
    "CFHR5_deficiency|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|C3_glomerulonephritis": 1,
    "Atypical_hemolytic-uremic_syndrome|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|not_specified|not_provided": 1,
    "not_provided|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|CFHR5_deficiency": 1,
    "C3_glomerulonephritis|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|C3_glomerulonephritis|not_provided|CFHR5_deficiency": 1,
    "CFHR5_deficiency|not_provided|Inborn_genetic_diseases|C3_glomerulonephritis": 1,
    "not_provided|CFHR5_deficiency|not_specified|CFH-Related_Dense_Deposit_Disease_/_Membranoproliferative_Glomerulonephritis_Type_II|Kidney_disorder": 1,
    "CFHR5-related_disorder": 1,
    "Factor_XIII|_b_subunit|_deficiency_of": 36,
    "not_provided|Factor_XIII|_b_subunit|_deficiency_of": 11,
    "F13B-related_disorder|Factor_XIII|_b_subunit|_deficiency_of": 4,
    "not_specified|F13B-related_disorder|Inborn_genetic_diseases|Factor_XIII|_b_subunit|_deficiency_of": 1,
    "not_provided|Factor_XIII|_b_subunit|_deficiency_of|not_specified": 2,
    "F13B-related_disorder": 4,
    "Factor_XIII|_b_subunit|_deficiency_of|not_specified": 1,
    "Hereditary_factor_XIII_deficiency_disease|not_specified|not_provided|Factor_XIII|_b_subunit|_deficiency_of": 1,
    "not_provided|F13B-related_disorder|Factor_XIII|_b_subunit|_deficiency_of": 1,
    "F13B-related_disorder|not_provided|Factor_XIII|_b_subunit|_deficiency_of": 2,
    "Inborn_genetic_diseases|Factor_XIII|_b_subunit|_deficiency_of": 2,
    "Factor_XIII_deficiency|Factor_XIII|_b_subunit|_deficiency_of": 1,
    "Factor_XIII|_b_subunit|_deficiency_of|not_provided": 1,
    "Factor_XIII|_b_subunit|_deficiency_of|not_provided|Venous_thrombosis|_susceptibility_to|not_specified": 1,
    "Coagulation_factor_deficiency_syndrome|Factor_XIII|_b_subunit|_deficiency_of|not_provided": 1,
    "not_specified|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 29,
    "Microcephaly_5|_primary|_autosomal_recessive": 253,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive": 95,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|not_specified": 12,
    "Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases": 9,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided": 69,
    "Inborn_genetic_diseases|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 16,
    "not_provided|Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive": 14,
    "Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive|not_provided": 19,
    "Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 11,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases": 12,
    "not_provided|not_specified|Microcephaly_5|_primary|_autosomal_recessive": 14,
    "ASPM-related_disorder|not_specified|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 8,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 15,
    "not_provided|ASPM-related_disorder|Microcephaly_5|_primary|_autosomal_recessive": 3,
    "not_specified|Microcephaly_5|_primary|_autosomal_recessive|not_provided": 15,
    "ASPM-related_disorder|not_provided": 4,
    "not_specified|Microcephaly_5|_primary|_autosomal_recessive|ASPM-related_disorder|not_provided": 3,
    "See_cases|Microcephaly_5|_primary|_autosomal_recessive|not_provided": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|Intellectual_disability": 2,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "ASPM-related_disorder": 7,
    "ASPM-related_disorder|not_specified|not_provided": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided|ASPM-related_disorder": 1,
    "Microcephaly|Lissencephaly|not_provided|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided|Autosomal_recessive_primary_microcephaly": 1,
    "not_specified|ASPM-related_disorder|not_provided": 1,
    "ASPM-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 3,
    "Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases|ASPM-related_disorder|not_provided": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided|See_cases": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases|Autosomal_recessive_primary_microcephaly|not_provided": 1,
    "Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive|not_specified": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|not_provided|not_specified": 7,
    "Microcephaly_5|_primary|_autosomal_recessive|not_specified|not_provided": 8,
    "not_provided|not_specified|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "ASPM-related_disorder|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 5,
    "Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive": 4,
    "Inborn_genetic_diseases|not_specified|not_provided|ASPM-related_disorder|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|ASPM-related_disorder|not_provided": 3,
    "Microcephaly_1|_primary|_autosomal_recessive": 89,
    "Intellectual_disability|Microcephaly_5|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "ASPM-related_disorder|Inborn_genetic_diseases|not_provided|Microcephaly_5|_primary|_autosomal_recessive|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|ASPM-related_disorder|not_provided|Microcephaly_5|_primary|_autosomal_recessive|Intellectual_disability": 1,
    "not_provided|ASPM-related_disorder|Microcephaly_5|_primary|_autosomal_recessive|not_specified": 1,
    "Autosomal_recessive_primary_microcephaly|Microcephaly_5|_primary|_autosomal_recessive|not_provided|ASPM-related_disorder": 1,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|ASPM-related_disorder": 2,
    "ASPM-related_disorder|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 6,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|ASPM-related_disorder|Inborn_genetic_diseases|Primary_Microcephaly|_Recessive": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "not_provided|ASPM-related_disorder": 5,
    "not_specified|not_provided|ASPM-related_disorder|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|Autosomal_recessive_primary_microcephaly|not_provided": 1,
    "ASPM-related_disorder|not_provided|Microcephaly_5|_primary|_autosomal_recessive|Intellectual_disability": 1,
    "not_specified|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "ASPM-related_disorder|Microcephaly_5|_primary|_autosomal_recessive|not_specified|not_provided": 1,
    "ASPM-related_disorder|not_provided|not_specified|Microcephaly_5|_primary|_autosomal_recessive": 2,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_provided": 7,
    "Microcephaly_5|_primary|_autosomal_recessive|Autosomal_recessive_primary_microcephaly": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "not_provided|Autosomal_recessive_primary_microcephaly|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_5|_primary|_autosomal_recessive|not_specified": 2,
    "not_specified|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_primary_microcephaly|Microcephaly|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "not_specified|not_provided|Microcephaly_5|_primary|_autosomal_recessive|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive|not_provided|Intellectual_disability": 1,
    "not_provided|not_specified|ASPM-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Microcephaly_5|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|Microcephaly_5|_primary|_autosomal_recessive": 2,
    "ASPM-related_disorder|Inborn_genetic_diseases|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|Microcephaly_5|_primary|_autosomal_recessive|not_provided": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "not_provided|Primary_Microcephaly|_Recessive": 2,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|not_specified|ASPM-related_disorder": 1,
    "Autosomal_recessive_primary_microcephaly|Microcephaly_5|_primary|_autosomal_recessive|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|ASPM-related_disorder|not_provided|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Microcephaly_5|_primary|_autosomal_recessive|not_provided|not_specified": 1,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|Abnormality_of_the_nervous_system": 1,
    "not_provided|Microcephaly_5|_primary|_autosomal_recessive|Microcephaly": 1,
    "Autosomal_recessive_primary_microcephaly|not_provided": 2,
    "Microcephaly_5|_primary|_autosomal_recessive|Abnormality_of_the_nervous_system": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|not_specified|ASPM-related_disorder|not_provided": 2,
    "not_provided|not_specified|Microcephaly_5|_primary|_autosomal_recessive|ASPM-related_disorder": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|ASPM-related_disorder|not_specified|not_provided": 1,
    "not_specified|Microcephaly_5|_primary|_autosomal_recessive": 1,
    "Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8": 9,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa": 6,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 584,
    "Hereditary_macular_dystrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 549,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|not_provided": 2,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 5,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Leber_congenital_amaurosis_8": 82,
    "Retinitis_pigmentosa_12": 24,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_12|not_provided": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 18,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Autosomal_recessive_retinitis_pigmentosa|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 8,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 16,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa": 2,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis": 25,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|Retinitis_pigmentosa_12": 1,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 6,
    "Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Intellectual_disability|Retinal_dystrophy|Leber_congenital_amaurosis|not_provided": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinitis_pigmentosa|Hereditary_macular_dystrophy|CRB1-related_disorder": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 22,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_12": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Leber_congenital_amaurosis": 3,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Inborn_genetic_diseases|Retinitis_pigmentosa_12|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_1": 63,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 13,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa": 3,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 19,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Inborn_genetic_diseases": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided": 8,
    "CRB1-related_disorder|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified|not_provided|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "CRB1-related_disorder|CRB1-related_maculopathy|Macular_dystrophy|Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified|not_provided|Leber_congenital_amaurosis_1|Autosomal_recessive_bestrophinopathy|Cone_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|CRB1-related_disorder": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy": 7,
    "Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 6,
    "Retinal_dystrophy|Abnormality_of_the_eye": 2,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 3,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Retinal_dystrophy|Macular_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinal_dystrophy": 3,
    "not_specified|not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_1": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Intellectual_disability|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_1": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 4,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|CRB1-related_disorder": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy": 10,
    "Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 6,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy": 5,
    "CRB1-related_disorder|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|not_provided|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|CRB1-related_disorder": 3,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Pigmented_paravenous_retinochoroidal_atrophy": 3,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 4,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_8|Retinal_dystrophy|Retinitis_pigmentosa_12": 1,
    "not_provided|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_specified": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 3,
    "not_provided|Inborn_genetic_diseases|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "not_provided|CRB1-related_disorder|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Retinal_dystrophy|Retinitis_pigmentosa_12|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_8": 2,
    "Leber_congenital_amaurosis|Cone-rod_dystrophy": 2,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided": 1,
    "not_provided|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|not_specified|CRB1-related_disorder": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided": 9,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases": 1,
    "CRB1-related_disorder": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|CRB1-related_disorder|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis": 2,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 3,
    "not_specified|Leber_congenital_amaurosis_8": 2,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 2,
    "Retinitis_pigmentosa_12|Autosomal_recessive_retinitis_pigmentosa|Leber_congenital_amaurosis_8|not_provided": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Leber_congenital_amaurosis_8|Retinal_dystrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa_12": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa|not_specified": 1,
    "Inborn_genetic_diseases|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 2,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis": 3,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 1,
    "not_provided|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_1|not_specified|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 3,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|Leber_congenital_amaurosis": 2,
    "not_specified|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|not_specified|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Macular_dystrophy|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_12": 2,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_13": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided": 1,
    "not_provided|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "CRB1-related_maculopathy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "not_provided|Pigmented_paravenous_retinochoroidal_atrophy|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases": 7,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Inborn_genetic_diseases": 2,
    "Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|not_provided": 2,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided": 2,
    "Retinal_dystrophy|not_specified|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Intellectual_disability|Leber_congenital_amaurosis_8": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 3,
    "Cone-rod_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided": 1,
    "Optic_atrophy|not_provided|Cone-rod_dystrophy": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_8|not_provided|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|not_provided": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified": 1,
    "not_specified|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_12": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Leber_congenital_amaurosis_8": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|not_provided": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|not_provided|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "CRB1-related_disorder|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 2,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "CRB1-related_disorder|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Hereditary_macular_dystrophy": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified|not_provided|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Early-onset_retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinal_dystrophy|not_provided|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|not_provided|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|CRB1-related_disorder": 3,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|not_provided": 1,
    "CRB1-related_disorder|CRB1-related_maculopathy|Macular_dystrophy|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa-deafness_syndrome|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Leber_congenital_amaurosis": 1,
    "CRB1-related_maculopathy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Leber_congenital_amaurosis|Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "CRB1-related_disorder|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinal_dystrophy|not_provided|not_specified|Leber_congenital_amaurosis|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Leber_congenital_amaurosis_8|not_specified": 1,
    "CRB1-related_disorder|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_8": 1,
    "not_provided|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|not_specified": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis_8": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis|not_provided|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_1|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|CRB1-related_disorder|not_specified|Hereditary_macular_dystrophy|Retinal_dystrophy": 1,
    "not_provided|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis_1|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_8|Retinal_dystrophy": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "not_specified|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 2,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa|Retinitis_pigmentosa_12|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_specified": 3,
    "not_provided|Early-onset_retinal_dystrophy|Leber_congenital_amaurosis_8": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Hereditary_macular_dystrophy|CRB1-related_disorder|Optic_atrophy|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|not_specified|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided": 1,
    "Macular_dystrophy|Retinal_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_12|Autosomal_recessive_retinitis_pigmentosa": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_8|Retinal_dystrophy|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_12|Inborn_genetic_diseases|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Leber_congenital_amaurosis": 1,
    "not_specified|Retinitis_pigmentosa|Leber_congenital_amaurosis_8": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Inborn_genetic_diseases|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Leber_congenital_amaurosis": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_1|CRB1-related_disorder|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy": 1,
    "not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12": 1,
    "Hereditary_macular_dystrophy|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|CRB1-related_disorder|Retinal_dystrophy|not_provided|Cone_dystrophy": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 3,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12": 2,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|Leber_congenital_amaurosis|CRB1-related_disorder": 1,
    "Cone-rod_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 2,
    "not_provided|Retinitis_pigmentosa_12": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis": 3,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Pigmented_paravenous_retinochoroidal_atrophy": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy": 3,
    "Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_8|not_provided": 3,
    "Retinitis_pigmentosa|Retinal_dystrophy|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided|CRB1-related_disorder|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 2,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_specified": 2,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Stargardt_disease|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 2,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|not_provided": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Early-onset_retinal_dystrophy|Leber_congenital_amaurosis|Retinal_dystrophy|not_provided": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_8|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Hereditary_macular_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Leber_congenital_amaurosis_1|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|not_provided": 1,
    "Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8": 2,
    "Leber_congenital_amaurosis|not_provided": 20,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|not_specified": 1,
    "not_provided|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_1|not_specified": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|CRB1-related_disorder|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa|Hereditary_macular_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy": 1,
    "CRB1-related_disorder|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Inborn_genetic_diseases|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "not_provided|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinal_dystrophy": 1,
    "Cone-rod_dystrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "not_specified|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided": 1,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_1": 1,
    "not_provided|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|Retinal_dystrophy": 1,
    "CRB1-related_disorder|not_specified|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Leber_congenital_amaurosis|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_1|Pigmented_paravenous_retinochoroidal_atrophy": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_specified|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Retinal_dystrophy": 1,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|not_provided": 1,
    "Leber_congenital_amaurosis|Hereditary_macular_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|Pigmented_paravenous_retinochoroidal_atrophy|not_provided": 1,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_specified": 1,
    "Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa_12|not_specified": 1,
    "Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12|not_provided|Leber_congenital_amaurosis": 1,
    "not_specified|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Leber_congenital_amaurosis_8|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Hereditary_macular_dystrophy|Leber_congenital_amaurosis_8|Retinitis_pigmentosa_12": 1,
    "Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Inborn_genetic_diseases|Leber_congenital_amaurosis|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8": 1,
    "Retinitis_pigmentosa|Pigmented_paravenous_retinochoroidal_atrophy|not_specified|Retinitis_pigmentosa_12|Leber_congenital_amaurosis_8|not_provided": 1,
    "Pigmented_paravenous_retinochoroidal_atrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_8": 1,
    "Retinitis_Pigmentosa|_Recessive|Pigmented_paravenous_retinochoroidal_atrophy|Leber_congenital_amaurosis": 1,
    "not_specified|Immunodeficiency_104": 15,
    "Immunodeficiency_104": 1335,
    "Immunodeficiency_104|not_provided": 41,
    "Immunodeficiency_104|not_provided|not_specified|PTPRC-related_disorder": 1,
    "Immunodeficiency_104|Inborn_genetic_diseases": 47,
    "not_provided|Immunodeficiency_104": 15,
    "not_specified|Immunodeficiency_105|PTPRC_POLYMORPHISM|not_provided|Immunodeficiency_104": 1,
    "Inborn_genetic_diseases|Immunodeficiency_104|Hepatitis_C_virus|_susceptibility_to": 1,
    "Immunodeficiency_105|Immunodeficiency_104|Inborn_genetic_diseases": 1,
    "Immunodeficiency_104|Immunodeficiency_105": 3,
    "Inborn_genetic_diseases|Immunodeficiency_104|Immunodeficiency_105": 1,
    "not_specified|not_provided|Immunodeficiency_104": 9,
    "Inborn_genetic_diseases|Immunodeficiency_104": 28,
    "Inborn_genetic_diseases|Immunodeficiency_104|not_provided": 1,
    "Immunodeficiency_104|not_provided|Inborn_genetic_diseases": 1,
    "PTPRC-related_disorder|not_specified|not_provided|Immunodeficiency_104": 1,
    "not_specified|Immunodeficiency_105|not_provided|Immunodeficiency_104": 1,
    "Hepatitis_C_virus|_susceptibility_to|Immunodeficiency_104": 1,
    "Immunodeficiency_104|Hepatitis_C_virus|_susceptibility_to": 1,
    "PTPRC-related_disorder|not_provided|Immunodeficiency_104": 1,
    "Immunodeficiency_105|Inborn_genetic_diseases|Immunodeficiency_104": 1,
    "Immunodeficiency_104|PTPRC-related_disorder|not_provided": 2,
    "Immunodeficiency_104|not_specified": 9,
    "Immunodeficiency_105|Immunodeficiency_104|Hepatitis_C_virus|_susceptibility_to": 1,
    "Immunodeficiency_104|Hepatitis_C_virus|_susceptibility_to|not_specified|PTPRC-related_disorder|not_provided": 1,
    "Immunodeficiency_105": 6,
    "not_provided|PTPRC-related_disorder|Immunodeficiency_104": 1,
    "not_provided|Immunodeficiency_104|PTPRC-related_disorder": 1,
    "Immunodeficiency_105|Immunodeficiency_104|PTPRC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Immunodeficiency_104|PTPRC-related_disorder": 3,
    "not_provided|Immunodeficiency_104|Inborn_genetic_diseases": 1,
    "Immunodeficiency_105|Immunodeficiency_104": 1,
    "not_provided|not_specified|Immunodeficiency_104": 3,
    "Immunodeficiency_104|Immunodeficiency_105|PTPRC-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Immunodeficiency_104": 2,
    "Inborn_genetic_diseases|Immunodeficiency_104|Immunodeficiency_105|not_provided|PTPRC-related_disorder": 1,
    "Hepatitis_C_virus|_susceptibility_to|Immunodeficiency_104|not_provided": 1,
    "Immunodeficiency_104|not_provided|Hepatitis_C_virus|_susceptibility_to": 1,
    "not_provided|Immunodeficiency_104|Immunodeficiency_105": 1,
    "PTPRC-related_disorder|Immunodeficiency_104": 2,
    "Immunodeficiency_105|Immunodeficiency_104|not_provided|not_specified": 1,
    "Immunodeficiency_104|not_provided|PTPRC-related_disorder": 1,
    "not_provided|Immunodeficiency_104|Immunodeficiency_105|Hepatitis_C_virus|_susceptibility_to|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|See_cases|Immunodeficiency_104": 1,
    "Immunodeficiency_104|not_specified|not_provided|PTPRC-related_disorder": 1,
    "Immunodeficiency_104|not_provided|not_specified": 1,
    "PTPRC-related_disorder": 1,
    "not_specified|not_provided|Acute_myeloblastic_leukemia_with_maturation": 5,
    "not_specified|Premature_ovarian_failure": 3,
    "Anophthalmia-microphthalmia_syndrome": 168,
    "Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|Microcephaly_20|_primary|_autosomal_recessive|not_provided": 2,
    "KIF14-related_disorder": 7,
    "not_provided|Inborn_genetic_diseases|KIF14-related_disorder": 1,
    "Microcephaly_20|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "Microcephaly_20|_primary|_autosomal_recessive|Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|not_provided": 1,
    "KIF14-related_disorder|not_specified": 1,
    "Microcephaly_20|_primary|_autosomal_recessive": 20,
    "Microcephaly_20|_primary|_autosomal_recessive|Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome": 9,
    "Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome": 5,
    "Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|not_provided": 1,
    "Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|Microcephaly_20|_primary|_autosomal_recessive": 1,
    "Microcephaly_20|_primary|_autosomal_recessive|Joubert_syndrome_and_related_disorders": 1,
    "KIF14-related_disorder|Joubert_syndrome_and_related_disorders|not_provided": 1,
    "KIF14-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KIF14-related_disorder|not_provided": 2,
    "not_provided|Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|Microcephaly_20|_primary|_autosomal_recessive": 2,
    "Joubert_syndrome_and_related_disorders|not_provided": 3,
    "not_provided|KIF14-related_disorder": 1,
    "Inborn_genetic_diseases|Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|not_provided|KIF14-related_disorder|Microcephaly_20|_primary|_autosomal_recessive": 2,
    "not_provided|Microcephaly_20|_primary|_autosomal_recessive": 2,
    "Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|Microcephaly_20|_primary|_autosomal_recessive|not_specified|not_provided|KIF14-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly_20|_primary|_autosomal_recessive": 1,
    "KIF14-related_disorder|Microcephaly_20|_primary|_autosomal_recessive|Lethal_fetal_cerebrorenogenitourinary_agenesis/hypoplasia_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|KIF14-related_disorder": 1,
    "KIF14-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Microcephaly_20|_primary|_autosomal_recessive": 1,
    "DDX59-related_disorder": 3,
    "Orofaciodigital_syndrome_V": 6,
    "DDX59-related_disorder|not_provided": 4,
    "Orofaciodigital_syndrome_V|not_provided": 2,
    "not_provided|Orofaciodigital_syndrome_V": 2,
    "DDX59-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|DDX59-related_disorder": 4,
    "Inborn_genetic_diseases|DDX59-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Orofaciodigital_syndrome_V": 1,
    "Premature_ovarian_insufficiency|not_provided": 7,
    "Inflammatory_bowel_disease_29": 4,
    "Neurodevelopmental_disorder|not_specified": 5,
    "KIF21B-related_Neurodevelopmental_disorder": 1,
    "KIF21B-related_disorder": 6,
    "See_cases|Long_QT_syndrome": 1,
    "KIF21B-related_Neurodevelopmental_disorder|not_specified": 1,
    "KIF21B-associated_neurodevelopmental_disorder": 1,
    "Moderate_global_developmental_delay|Cerebral_ischemia|Hypotonia|Macrogyria": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 2,
    "Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis": 3,
    "Hypokalemic_periodic_paralysis|_type_1": 39,
    "Hypokalemic_periodic_paralysis|_type_1|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5": 543,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 506,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 775,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 65,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided": 26,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 4,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 4,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 14,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|not_provided|Congenital_myopathy_18|Malignant_hyperthermia_of_anesthesia": 1,
    "CACNA1S-related_disorder|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 4,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 8,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|not_specified": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 13,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided": 4,
    "Congenital_myopathy_18|CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5": 9,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Malignant_hyperthermia_of_anesthesia": 23,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 8,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 12,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5": 11,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 7,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18": 7,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 10,
    "CACNA1S-related_disorder": 12,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|CACNA1S-related_disorder|not_specified": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1": 5,
    "CACNA1S-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 30,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|Congenital_myopathy_18": 2,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 2,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5": 5,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1": 5,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 21,
    "CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 6,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5": 8,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 19,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 3,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 10,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 4,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 4,
    "Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|CACNA1S-related_disorder|not_provided": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 3,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder|Congenital_myopathy_18": 2,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 16,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided": 2,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1": 2,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18|Inborn_genetic_diseases": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|CACNA1S-related_disorder": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5": 2,
    "Congenital_myopathy_18|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|CACNA1S-related_disorder|Congenital_myopathy_18": 1,
    "CACNA1S-related_disorder|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Centronuclear_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 2,
    "Hypokalemic_periodic_paralysis|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Inborn_genetic_diseases|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 2,
    "not_provided|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 3,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 4,
    "Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder": 5,
    "CACNA1S-related_disorder|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5": 4,
    "CACNA1S-related_disorder|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Congenital_myopathy_18|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis": 1,
    "Congenital_myopathy_18": 7,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided": 4,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|not_specified": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 9,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 5,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Congenital_myopathy_18": 3,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 8,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|Congenital_myopathy_18": 2,
    "Inborn_genetic_diseases|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 3,
    "Congenital_myopathy_18|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 3,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder|Congenital_myopathy_18": 1,
    "Congenital_myopathy": 21,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified": 6,
    "Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 6,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18": 8,
    "not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 1,
    "not_provided|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 3,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 7,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 21,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_specified": 3,
    "CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5": 5,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 3,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 6,
    "Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Inborn_genetic_diseases": 3,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases|Congenital_myopathy_18|not_provided": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 5,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "not_provided|Congenital_myopathy_18": 2,
    "CACNA1S-related_disorder|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 3,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Congenital_myopathy_18": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 3,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|not_provided|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 6,
    "Hypokalemic_periodic_paralysis|_type_1|not_provided|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 3,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Congenital_myopathy_18|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|Congenital_myopathy_18": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|not_specified|not_provided": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|CACNA1S-related_disorder": 1,
    "CACNA1S-related_disorder|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Inborn_genetic_diseases": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1": 3,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|CACNA1S-related_disorder|Congenital_myopathy_18": 3,
    "not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18": 2,
    "not_provided|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Malignant_hyperthermia_of_anesthesia": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Inborn_genetic_diseases": 2,
    "CACNA1S-related_disorder|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "not_provided|not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_5": 3,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|Congenital_myopathy_18": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Congenital_myopathy_18|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 7,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|CACNA1S-related_disorder": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Hypokalemic_periodic_paralysis|_type_1": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided|Intellectual_disability": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 5,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "succinylcholine_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|CACNA1S-related_disorder": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 4,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5": 3,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified": 1,
    "Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|CACNA1S-related_disorder|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 2,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia_of_anesthesia|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia_of_anesthesia": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 4,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 17,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|not_provided|CACNA1S-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Congenital_myopathy_18": 2,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_provided": 3,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided": 5,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Congenital_myopathy_18|Inborn_genetic_diseases": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 4,
    "Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia_of_anesthesia|not_specified|Hypokalemic_periodic_paralysis|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|not_specified": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 3,
    "CACNA1S-related_disorder|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|not_specified": 1,
    "not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 2,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 3,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 4,
    "CACNA1S-related_disorder|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|not_provided": 2,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 2,
    "Congenital_myopathy_18|not_specified|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Congenital_myopathy_18|not_specified": 1,
    "CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|not_specified|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 3,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Muscular_atrophy|skeletal_contractures|Congenital_myopathy_18|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_provided|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|Congenital_myopathy_18": 2,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_provided|CACNA1S-related_disorder|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Centronuclear_myopathy": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|not_provided": 2,
    "not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided": 2,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_specified|Malignant_hyperthermia_of_anesthesia|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "CACNA1S-related_disorder|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_nuclear_cataract|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|CACNA1S-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18": 3,
    "Congenital_myopathy_18|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "CACNA1S-related_disorder|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder": 2,
    "CACNA1S-related_disorder|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Rhabdomyolysis|not_provided|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Congenital_myopathy_18|not_specified": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|CACNA1S-related_disorder": 1,
    "not_provided|CACNA1S-related_disorder|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "not_provided|not_specified|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "not_specified|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_18|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder|not_provided|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|Malignant_hyperthermia|_susceptibility_to|_5|not_provided": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 2,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|not_specified|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|Congenital_myopathy_18|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "not_provided|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Long_QT_syndrome|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5": 2,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|CACNA1S-related_disorder|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Hereditary_liability_to_pressure_palsies|not_provided": 1,
    "not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Congenital_myopathy_18|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|not_specified": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 4,
    "Malignant_hyperthermia|_susceptibility_to|_5|Malignant_hyperthermia_of_anesthesia": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Centronuclear_myopathy|Congenital_myopathy_18": 1,
    "not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_18|not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_specified|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Congenital_myopathy_18": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided|not_specified|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|Congenital_myopathy_18": 1,
    "Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|CACNA1S-related_disorder": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Hypokalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis": 2,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|not_specified|Hypokalemic_periodic_paralysis|_type_1|CACNA1S-related_disorder": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Long_QT_syndrome": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Malignant_hyperthermia_of_anesthesia|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Inborn_genetic_diseases|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|CACNA1S-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis|not_provided": 1,
    "Congenital_myopathy_18|not_provided|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis|_type_1|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Congenital_myopathy": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Malignant_hyperthermia_of_anesthesia|not_specified|Hypokalemic_periodic_paralysis|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|CACNA1S-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5": 1,
    "CACNA1S-related_disorder|Hypokalemic_periodic_paralysis|_type_1|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Malignant_hyperthermia|_susceptibility_to|_5|Congenital_myopathy_18|not_provided|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|not_specified|not_provided|Congenital_myopathy_18|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided": 1,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_1|not_provided|Malignant_hyperthermia_of_anesthesia|Congenital_myopathy_18|Hypokalemic_periodic_paralysis|_type_1|Malignant_hyperthermia|_susceptibility_to|_5|Hypokalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis": 4,
    "not_provided|Hypokalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|not_provided|Malignant_hyperthermia_of_anesthesia|Hypokalemic_periodic_paralysis|_type_1|Congenital_myopathy_18|Malignant_hyperthermia|_susceptibility_to|_5|Thyrotoxic_periodic_paralysis|_susceptibility_to|_1": 1,
    "Teeth|_odd_shapes_of": 1,
    "Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 97,
    "Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_provided": 6,
    "Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Inborn_genetic_diseases": 2,
    "PKP1-related_disorder": 3,
    "not_provided|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 38,
    "PKP1-related_disorder|not_provided|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 4,
    "not_provided|PKP1-related_disorder|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "PKP1-related_disorder|not_provided": 2,
    "Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_provided": 1,
    "not_provided|PKP1-related_disorder": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Dilated_Cardiomyopathy|_Dominant|Familial_restrictive_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_provided": 1,
    "not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_provided": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 40,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 20,
    "Cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D": 4,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy|not_provided": 2,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 11,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided": 7,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 114,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D": 48,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 46,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_provided": 4,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided|not_specified|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Costello_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1DD": 941,
    "TNNT2-related_disorder|not_provided": 1,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 3,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 19,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided": 2,
    "not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Hypertrophic_cardiomyopathy_7": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_2": 2,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified": 1,
    "not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|not_provided": 3,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 23,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified|Cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 1,
    "Hypertrophic_cardiomyopathy|not_provided": 197,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 2,
    "not_provided|TNNT2-related_disorder|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 338,
    "not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 9,
    "Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype": 10,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Primary_dilated_cardiomyopathy": 3,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 2,
    "not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_provided|Dilated_cardiomyopathy_1D": 1,
    "not_specified|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|not_provided|Dilated_cardiomyopathy_1D": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Primary_familial_dilated_cardiomyopathy|not_specified": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "not_provided|TNNT2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_specified": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 3,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_provided": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 11,
    "Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 3,
    "not_specified|Sudden_cardiac_death|Cardiomyopathy|Cardiovascular_phenotype|TNNT2-related_disorder|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Familial_restrictive_cardiomyopathy|not_specified|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "not_provided|not_specified|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "TNNT2-related_disorder|not_specified|not_provided|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Dilated_Cardiomyopathy|_Dominant": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 3,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|not_specified|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 2,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|not_provided": 1,
    "Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided|Cardiovascular_phenotype": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Familial_restrictive_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 12,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D": 4,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified": 3,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S": 41,
    "Primary_dilated_cardiomyopathy|TNNT2-related_disorder|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1D": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D": 2,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|See_cases|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1D|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|TNNT2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 4,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 10,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|not_specified": 2,
    "not_specified|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 1,
    "Cardiomyopathy|_familial_restrictive|_3|not_specified|not_provided|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|Left_ventricular_noncompaction_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|Hypertrophic_cardiomyopathy_2": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 3,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 2,
    "Left_ventricular_noncompaction": 8,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 1,
    "not_specified|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1DD|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|not_provided|not_specified": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1D|not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 2,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 3,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1DD": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|not_specified": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_congenital_ichthyosis_1": 210,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|not_provided|not_specified|TNNT2-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_provided|not_specified|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype": 4,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|TNNT2-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1DD|Dilated_cardiomyopathy_1D|Primary_dilated_cardiomyopathy|Myocarditis|not_specified|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Familial_isolated_dilated_cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "TNNT2-related_disorder|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified|not_provided|Cardiomyopathy|_familial_restrictive|_3|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified|not_provided|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Primary_dilated_cardiomyopathy|TNNT2-related_disorder": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|TNNT2-related_disorder|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|not_specified": 1,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Familial_restrictive_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified": 37,
    "See_cases|not_provided|not_specified|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Restrictive_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2": 1,
    "TNNT2-related_disorder|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 2,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_familial_hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_provided": 1,
    "not_provided|not_specified|TNNT2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 1,
    "TNNT2-related_disorder|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|TNNT2-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified": 1,
    "Hypokinetic_non-dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|_familial_restrictive|_3|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Familial_restrictive_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|not_specified|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "not_specified|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|not_specified": 3,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Left_ventricular_noncompaction_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1D|TNNT2-related_disorder|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|not_specified": 1,
    "Cardiovascular_phenotype|Increased_left_ventricular_wall_thickness|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Primary_familial_hypertrophic_cardiomyopathy|Supraventricular_tachycardia": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Sudden_unexplained_death|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified": 1,
    "TNNT2-related_disorder|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|not_specified|Cardiomyopathy|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_specified": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Left_ventricular_hypertrophy": 3,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|TNNT2-related_disorder": 1,
    "not_provided|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2": 1,
    "not_specified|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1D|Cardiomyopathy|_familial_restrictive|_3": 1,
    "not_provided|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_3|Cardiomyopathy|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided": 6,
    "Cardiomyopathy|_familial_restrictive|_3|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "TNNT2-related_disorder": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Familial_restrictive_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1D|Hypertrophic_cardiomyopathy_2|Cardiomyopathy|_familial_restrictive|_3": 1,
    "TNNI1-related_congenital_myopathy": 1,
    "IPO9-related_condition": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_3": 4,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_3|Visceral_myopathy_1": 1,
    "LMOD1-related_condition": 1,
    "Fanconi_anemia_complementation_group_T": 6,
    "not_provided|Fanconi_anemia_complementation_group_T": 2,
    "Congenital_lactic_acidosis": 2,
    "SYT2-related_disorder": 2,
    "SYT2-related_disorder|not_provided": 4,
    "Myasthenic_syndrome|_congenital|_7B|_presynaptic|_autosomal_recessive": 5,
    "Congenital_myasthenic_syndrome_7": 7,
    "not_provided|Congenital_myasthenic_syndrome_7": 3,
    "Muscle_weakness|Respiratory_distress": 1,
    "not_provided|Myasthenic_syndrome|_congenital|_7B|_presynaptic|_autosomal_recessive|Congenital_myasthenic_syndrome_7": 2,
    "not_provided|SYT2-related_myasthenia": 1,
    "not_provided|Congenital_myasthenic_syndrome_7|Inborn_genetic_diseases": 1,
    "not_provided|SYT2-related_disorder": 2,
    "not_provided|Congenital_myasthenic_syndrome_7|Myasthenic_syndrome|_congenital|_7B|_presynaptic|_autosomal_recessive": 1,
    "Congenital_myasthenic_syndrome_7|not_provided|Myasthenic_syndrome|_congenital|_7B|_presynaptic|_autosomal_recessive": 1,
    "Myasthenic_syndrome|_congenital|_7B|_presynaptic|_autosomal_recessive|Congenital_myasthenic_syndrome_7": 1,
    "Peripheral_axonal_neuropathy": 2,
    "Congenital_myasthenic_syndrome_7|not_provided": 1,
    "Inborn_genetic_diseases|SYT2-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_65": 53,
    "KDM5B-related_disorder": 19,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_65": 1,
    "Inborn_genetic_diseases|KDM5B-related_disorder": 2,
    "KDM5B-related_disorder|not_provided": 5,
    "Autism_spectrum_disorder|Intellectual_disability|_autosomal_recessive_65": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_65": 5,
    "KDM5B-related_disorder|Intellectual_disability|_autosomal_recessive_65": 1,
    "not_provided|KDM5B-related_disorder": 4,
    "Intellectual_disability|_autosomal_recessive_65|not_provided": 9,
    "not_provided|Intellectual_disability|_autosomal_recessive_65|KDM5B-related_disorder": 1,
    "KDM5B-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_65|Inborn_genetic_diseases": 3,
    "Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype": 3,
    "not_provided|KDM5B-related_disorder|Inborn_genetic_diseases": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia": 7,
    "KDM5B-related_disorder|Intellectual_disability|_autosomal_recessive_65|not_provided": 1,
    "ADIPOR1-related_disorder": 1,
    "not_provided|ADORA1-related_disorder": 1,
    "not_specified|ADORA1-related_disorder|not_provided": 1,
    "ADORA1-related_disorder": 2,
    "Asthma-related_traits|_susceptibility_to|_7": 1,
    "Chitotriosidase_deficiency": 125,
    "not_provided|Chitotriosidase_deficiency": 9,
    "not_specified|Chitotriosidase_deficiency": 14,
    "Chitotriosidase_deficiency|not_provided": 14,
    "Chitotriosidase_deficiency|not_specified": 10,
    "Chitotriosidase_deficiency|not_specified|not_provided": 2,
    "PRELP-related_osteosclerosis": 1,
    "not_provided|OPTC-related_disorder": 1,
    "OPTC-related_disorder": 3,
    "not_provided|ATP2B4-related_disorder": 11,
    "ATP2B4-related_disorder|not_provided": 4,
    "ATP2B4-related_disorder": 9,
    "not_specified|ATP2B4-related_disorder": 1,
    "ATP2B4-related_disorder|not_specified|not_provided": 1,
    "SNRPE-related_disorder": 3,
    "not_provided|Hypotrichosis_11": 1,
    "Hypotrichosis_11": 3,
    "SNRPE-related_disorder|Hypotrichosis_11": 1,
    "Long_QT_syndrome_1": 269,
    "not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin": 4,
    "not_provided|Hepatoblastoma|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2": 11,
    "Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2|Inborn_genetic_diseases": 4,
    "Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2": 23,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases|not_provided": 2,
    "HYPERPRORENINEMIA|_FAMILIAL": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis": 6,
    "Renal_tubular_dysgenesis|Inborn_genetic_diseases|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "Renal_tubular_dysgenesis|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2": 6,
    "not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases": 1,
    "not_provided|REN-related_disorder": 3,
    "Renal_tubular_dysgenesis|not_provided|REN-related_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "Renal_tubular_dysgenesis|Familial_juvenile_hyperuricemic_nephropathy_type_2": 3,
    "Inborn_genetic_diseases|Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "REN-related_disorder|not_provided": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 2,
    "Renal_tubular_dysgenesis": 145,
    "Renal_tubular_dysgenesis|Inborn_genetic_diseases|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "Inborn_genetic_diseases|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|not_provided|Renal_tubular_dysgenesis": 1,
    "REN-related_disorder": 4,
    "REN-related_disorder|Renal_tubular_dysgenesis|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2": 2,
    "Kidney_disorder|Renal_tubular_dysgenesis|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "REN-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2": 2,
    "Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2|not_provided": 4,
    "Kidney_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis|not_specified|not_provided": 1,
    "Kidney_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|not_provided|Renal_tubular_dysgenesis|not_specified": 1,
    "not_provided|Renal_tubular_dysgenesis|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "not_provided|REN-related_disorder|Inborn_genetic_diseases": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|not_provided|Inborn_genetic_diseases": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|REN-related_disorder|Inborn_genetic_diseases|Renal_tubular_dysgenesis|not_provided": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|not_provided|Renal_tubular_dysgenesis_of_genetic_origin": 2,
    "Intellectual_disability|_X-linked_61|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Nephrotic_syndrome": 2,
    "not_specified|not_provided|Renal_tubular_dysgenesis|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis|not_provided": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis": 1,
    "not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2|Renal_tubular_dysgenesis": 1,
    "not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_2|REN-related_disorder|Renal_tubular_dysgenesis": 1,
    "Kidney_failure": 5,
    "REN-related_disorder|Kidney_disorder|Renal_tubular_dysgenesis|not_specified|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_2": 1,
    "Hypogonadotropic_hypogonadism_13_with_or_without_anosmia|not_provided|not_specified": 1,
    "Hypogonadotropic_hypogonadism_13_with_or_without_anosmia": 2,
    "Disorder_of_sexual_differentiation|not_specified": 1,
    "not_provided|Hypogonadotropic_hypogonadism_13_with_or_without_anosmia|not_specified": 1,
    "not_specified|Hypogonadotropic_hypogonadism_13_with_or_without_anosmia|not_provided": 1,
    "KISS1-related_disorder": 2,
    "not_provided|KISS1-related_disorder": 1,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_2|not_provided": 3,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_2": 2,
    "not_provided|not_specified|PPP1R15B-related_disorder": 1,
    "not_provided|PPP1R15B-related_disorder|Inborn_genetic_diseases": 1,
    "PPP1R15B-related_disorder|not_provided": 4,
    "not_provided|PPP1R15B-related_disorder": 1,
    "PPP1R15B-related_disorder|not_specified|not_provided": 2,
    "not_provided|Microcephaly|_short_stature|_and_impaired_glucose_metabolism_2|PPP1R15B-related_disorder": 1,
    "PIK3C2B-related_disorder": 46,
    "not_specified|not_provided|PIK3C2B-related_disorder": 1,
    "PIK3C2B-related_disorder|not_provided": 3,
    "not_provided|PIK3C2B-related_disorder": 8,
    "not_specified|PIK3C2B-related_disorder": 1,
    "PIK3C2B-related_disorder|not_specified|not_provided": 1,
    "PIK3C2B-related_disorder|not_specified": 1,
    "Bone_marrow_failure_syndrome_6": 3,
    "Pfeiffer_syndrome|not_specified|Bone_marrow_failure_syndrome_6": 1,
    "MDM4-related_disorder|not_specified": 1,
    "not_provided|Bone_marrow_failure_syndrome_6": 1,
    "Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction": 27,
    "not_provided|NFASC-related_disorder|Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction": 1,
    "Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction|not_provided": 3,
    "NFASC-related_disorder|not_provided": 8,
    "NFASC-related_disorder": 21,
    "not_provided|NFASC-related_disorder": 5,
    "Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction": 1,
    "not_provided|Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction": 1,
    "Inborn_genetic_diseases|NFASC-related_disorder": 1,
    "NFASC-related_disorder|Inborn_genetic_diseases": 1,
    "NFASC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "NFASC-related_disorder|not_provided|Neurodevelopmental_disorder_with_central_and_peripheral_motor_dysfunction": 1,
    "Epilepsy|_familial_adult_myoclonic|_5": 671,
    "CNTN2-related_disorder|Epilepsy|_familial_adult_myoclonic|_5": 6,
    "not_specified|Epilepsy|_familial_adult_myoclonic|_5": 32,
    "Epilepsy|_familial_adult_myoclonic|_5|not_specified": 39,
    "Epilepsy|_familial_adult_myoclonic|_5|not_provided": 21,
    "CNTN2-related_disorder|Epilepsy|_familial_adult_myoclonic|_5|not_specified": 1,
    "Epilepsy|_familial_adult_myoclonic|_5|CNTN2-related_disorder": 2,
    "Epilepsy|_familial_adult_myoclonic|_5|CNTN2-related_disorder|not_provided": 1,
    "not_provided|Epilepsy|_familial_adult_myoclonic|_5": 14,
    "not_provided|CNTN2-related_disorder|Epilepsy|_familial_adult_myoclonic|_5": 1,
    "CNTN2-related_disorder": 1,
    "CNTN2-related_disorder|not_provided|Epilepsy|_familial_adult_myoclonic|_5": 1,
    "Epilepsy|_familial_adult_myoclonic|_1|Epilepsy|_familial_adult_myoclonic|_5|not_provided": 1,
    "CNTN2-related_disorder|Epilepsy|_familial_adult_myoclonic|_5|not_specified|not_provided": 1,
    "RBBP5-related_syndromic_neurodevelopmental_condition": 1,
    "Hereditary_spastic_paraplegia_23": 3,
    "Chronic_kidney_disease|not_provided": 6,
    "DSTYK-related_disorder|not_provided": 2,
    "DSTYK-related_disorder": 7,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1": 18,
    "DSTYK-related_disroder": 2,
    "not_provided|DSTYK-related_disorder": 5,
    "DSTYK-related_disorder|not_specified|not_provided": 2,
    "not_specified|Congenital_anomalies_of_kidney_and_urinary_tract_1|not_provided|Hereditary_spastic_paraplegia_23": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|Hereditary_spastic_paraplegia_23|not_provided": 1,
    "not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_1|Hereditary_spastic_paraplegia_23|not_specified": 1,
    "not_provided|not_specified|Congenital_anomalies_of_kidney_and_urinary_tract_1": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|not_provided": 3,
    "not_provided|DSTYK-related_disorder|Congenital_anomalies_of_kidney_and_urinary_tract_1": 1,
    "not_specified|DSTYK-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_23|Congenital_anomalies_of_kidney_and_urinary_tract_1|Complex_hereditary_spastic_paraplegia": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|Hereditary_spastic_paraplegia_23": 2,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|DSTYK-related_disorder|Hereditary_spastic_paraplegia_23|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_23": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|Hereditary_spastic_paraplegia_23|not_specified|not_provided": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|not_specified|not_provided": 1,
    "DSTYK-related_disorder|Congenital_anomalies_of_kidney_and_urinary_tract_1|not_provided": 1,
    "Anencephaly_2": 2,
    "NUAK2-related_disorder": 1,
    "RAB29-related_disorder": 2,
    "Nephronophthisis-like_nephropathy_2": 2,
    "not_provided|Nephronophthisis-like_nephropathy_2": 1,
    "Nephronophthisis-like_nephropathy_2|not_provided": 1,
    "RHEX-related_disorder": 9,
    "SRGAP2-associated_Neurodevelopmental_Disorder": 1,
    "Autoimmune_connective_tissue_disease_and_vasculitis|not_provided": 1,
    "Inflammatory_bowel_disease": 114,
    "Inflammatory_bowel_disease|not_provided": 6,
    "not_provided|Inflammatory_bowel_disease|not_specified": 2,
    "not_specified|Inflammatory_bowel_disease": 1,
    "IL10-related_early-onset_inflammatory_bowel_disease|Inflammatory_bowel_disease": 1,
    "not_provided|Inflammatory_bowel_disease": 2,
    "not_provided|Susceptibility_to_HIV_infection|Graft-versus-host_disease|_susceptibility_to|Rheumatoid_arthritis|Inflammatory_bowel_disease": 1,
    "Graft-versus-host_disease|_resistance_to|Susceptibility_to_HIV_infection|Cholangiocarcinoma|not_provided|Inflammatory_bowel_disease": 1,
    "Leprosy|_susceptibility_to|_1|Inflammatory_bowel_disease": 1,
    "Leprosy|_susceptibility_to|_1|Hepatitis_C_virus|_susceptibility_to": 1,
    "Rheumatoid_arthritis|_progression_of": 1,
    "IgA_glomerulonephritis": 1,
    "C4BPB-related_disorder": 2,
    "C4BPA-related_disorder": 6,
    "Protein-losing_enteropathy": 8,
    "CD55-related_disorder": 2,
    "not_provided|CD55-related_disorder|Protein-losing_enteropathy|Cromer_blood_group_system": 1,
    "Cromer_blood_group_system": 2,
    "Cromer_blood_group_system|not_provided": 1,
    "not_provided|CD55-related_disorder": 2,
    "Cromer_blood_group_system|Protein-losing_enteropathy|not_provided": 1,
    "CD55-related_disorder|not_provided": 4,
    "Protein-losing_enteropathy|CROMER_BLOOD_GROUP_SYSTEM|_Dr(a-)_PHENOTYPE": 1,
    "Cromer_blood_group_system|Protein-losing_enteropathy": 1,
    "not_provided|Cromer_blood_group_system|Protein-losing_enteropathy": 1,
    "Immunodeficiency|_common_variable|_7|not_provided": 24,
    "Immunodeficiency|_common_variable|_7": 554,
    "not_provided|Immunodeficiency|_common_variable|_7": 27,
    "CR2-related_disorder|not_provided|Immunodeficiency|_common_variable|_7": 1,
    "Immunodeficiency|_common_variable|_7|Inborn_genetic_diseases": 29,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_7": 29,
    "Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9|Immunodeficiency|_common_variable|_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency|_common_variable|_7": 2,
    "Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9": 3,
    "Immunodeficiency|_common_variable|_7|Immunodeficiency|_common_variable|_2|Systemic_lupus_erythematosus|_susceptibility_to|_9|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Immunodeficiency|_common_variable|_7": 1,
    "Immunodeficiency|_common_variable|_7|CR2-related_disorder|Inborn_genetic_diseases": 2,
    "Immunodeficiency|_common_variable|_7|not_specified|not_provided|Systemic_lupus_erythematosus|_susceptibility_to|_9|CR2-related_disorder": 1,
    "Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9|Inborn_genetic_diseases": 2,
    "CR2-related_disorder|Immunodeficiency|_common_variable|_7": 4,
    "not_provided|Immunodeficiency|_common_variable|_7|CR2-related_disorder": 1,
    "CR2-related_disorder|Systemic_lupus_erythematosus|_susceptibility_to|_9|Immunodeficiency|_common_variable|_2|Immunodeficiency|_common_variable|_7|not_provided": 1,
    "Immunodeficiency|_common_variable|_7|CR2-related_disorder": 7,
    "Inborn_genetic_diseases|CR2-related_disorder|Immunodeficiency|_common_variable|_7": 2,
    "not_provided|Immunodeficiency|_common_variable|_7|Inborn_genetic_diseases": 1,
    "Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9|not_provided|CR2-related_disorder": 1,
    "Immunodeficiency|_common_variable|_7|Inborn_genetic_diseases|not_provided": 2,
    "Immunodeficiency|_common_variable|_7|Joubert_syndrome_17": 1,
    "not_specified|Immunodeficiency|_common_variable|_7|CR2-related_disorder": 1,
    "Systemic_lupus_erythematosus|_susceptibility_to|_9": 1,
    "Immunodeficiency|_common_variable|_7|CR2-related_disorder|not_provided": 2,
    "not_provided|Systemic_lupus_erythematosus|_susceptibility_to|_9|Immunodeficiency|_common_variable|_7|Immunodeficiency|_common_variable|_2": 1,
    "Systemic_lupus_erythematosus|_susceptibility_to|_9|Immunodeficiency|_common_variable|_7": 2,
    "CR2-related_disorder|Immunodeficiency|_common_variable|_7|not_provided": 2,
    "not_provided|not_specified|Immunodeficiency|_common_variable|_7": 3,
    "Immunodeficiency|_common_variable|_7|not_specified|not_provided": 2,
    "not_specified|Immunodeficiency|_common_variable|_7|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_7|not_provided": 1,
    "Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9|Immunodeficiency|_common_variable|_2": 1,
    "CR2-related_disorder|Inborn_genetic_diseases|Immunodeficiency|_common_variable|_7": 1,
    "Immunodeficiency|_common_variable|_2": 216,
    "not_provided|CR2-related_disorder|Immunodeficiency|_common_variable|_7": 2,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_7|CR2-related_disorder": 1,
    "CR2-related_disorder": 4,
    "not_specified|Immunodeficiency|_common_variable|_7": 1,
    "Immunodeficiency|_common_variable|_7|not_specified": 1,
    "Immunodeficiency|_common_variable|_2|not_provided|Immunodeficiency|_common_variable|_7": 1,
    "not_specified|Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9|not_provided": 1,
    "Systemic_lupus_erythematosus|_susceptibility_to|_9|Immunodeficiency|_common_variable|_7|Immunodeficiency|_common_variable|_2|not_provided|CR2-related_disorder": 1,
    "not_provided|Immunodeficiency|_common_variable|_7|Systemic_lupus_erythematosus|_susceptibility_to|_9|CR2-related_disorder|Inborn_genetic_diseases": 1,
    "Immunodeficiency|_common_variable|_7|Immunodeficiency|_common_variable|_2|Systemic_lupus_erythematosus|_susceptibility_to|_9": 1,
    "KNOPS_BLOOD_GROUP_SYSTEM|Malaria|_susceptibility_to": 3,
    "KNOPS_BLOOD_GROUP_SYSTEM": 1,
    "Malaria|_severe|_resistance_to|CR1-related_disorder": 1,
    "CR1-related_disorder": 7,
    "not_provided|KNOPS_BLOOD_GROUP_SYSTEM": 1,
    "Malaria|_susceptibility_to|KNOPS_BLOOD_GROUP_SYSTEM|not_specified|not_provided": 1,
    "CR1-related_disorder|not_provided": 1,
    "not_provided|CR1-related_disorder": 2,
    "Polyarticular_arthritis|Anxiety|Hypothyroidism": 1,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 58,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided": 7,
    "CD46-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|CD46-related_disorder|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 2,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 15,
    "Atypical_hemolytic-uremic_syndrome|not_provided": 19,
    "CD46-related_disorder|not_provided": 5,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|CD46-related_disorder|not_provided": 3,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided|CD46-related_disorder": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided|Familial_Atypical_Hemolytic-Uremic_Syndrome": 1,
    "Thrombotic_microangiopathy|not_provided|Familial_Atypical_Hemolytic-Uremic_Syndrome": 1,
    "not_specified|Kidney_disorder|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|CD46-related_disorder|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided": 1,
    "not_provided|Kidney_disorder|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_specified|not_provided": 1,
    "not_provided|CD46-related_disorder": 5,
    "Familial_Atypical_Hemolytic-Uremic_Syndrome": 1,
    "Kidney_disorder|not_provided|not_specified|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 1,
    "Kidney_disorder|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 1,
    "CD46-related_disorder|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_provided": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|Myofibrillar_myopathy_6": 1,
    "Familial_Atypical_Hemolytic-Uremic_Syndrome|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_MCP/CD46_anomaly|not_specified|not_provided|CD46-related_disorder": 1,
    "not_provided|PLXNA2-related_disorder|not_specified": 10,
    "PLXNA2-related_disorder": 297,
    "not_provided|PLXNA2-related_disorder": 91,
    "PLXNA2-related_disorder|not_provided": 100,
    "not_specified|not_provided|PLXNA2-related_disorder": 7,
    "not_specified|PLXNA2-related_disorder": 25,
    "PLXNA2-related_disorder|not_provided|not_specified": 5,
    "PLXNA2-related_disorder|not_specified|not_provided": 10,
    "PLXNA2-related_disorder|Autism|not_provided": 1,
    "not_specified|PLXNA2-related_disorder|not_provided": 5,
    "PLXNA2-related_disorder|not_specified": 6,
    "not_provided|not_specified|PLXNA2-related_disorder": 6,
    "atypical_cerebral_palsy": 3,
    "not_provided|PLXNA2-related_disorder|Autism": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Amelogenesis_imperfecta_type_1A": 22,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa": 1,
    "Amelogenesis_imperfecta": 87,
    "Amelogenesis_imperfecta_type_1A|not_provided": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|not_specified": 3,
    "not_provided|LAMB3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|LAMB3-related_disorder|Junctional_epidermolysis_bullosa": 1,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Epidermolysis_bullosa": 1,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Junctional_epidermolysis_bullosa": 1,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 6,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A": 16,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 2,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|LAMB3-related_disorder|Junctional_epidermolysis_bullosa": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa": 2,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 2,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Inborn_genetic_diseases": 1,
    "not_specified|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa|not_provided": 1,
    "LAMB3-related_disorder|not_provided": 4,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A|not_provided|Junctional_epidermolysis_bullosa": 1,
    "not_provided|Inborn_genetic_diseases|LAMB3-related_disorder|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|not_provided": 2,
    "Junctional_epidermolysis_bullosa|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 5,
    "not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 7,
    "LAMB3-related_disorder|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa|not_provided": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|not_provided": 2,
    "not_specified|not_provided|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|not_provided|Junctional_epidermolysis_bullosa": 1,
    "not_specified|Junctional_epidermolysis_bullosa|not_provided": 1,
    "LAMB3-related_disorder|Junctional_epidermolysis_bullosa|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A": 5,
    "not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 2,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 2,
    "Junctional_epidermolysis_bullosa|not_provided|LAMB3-related_disorder": 3,
    "LAMB3-related_disorder|not_provided|Junctional_epidermolysis_bullosa": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "not_provided|not_specified|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Junctional_epidermolysis_bullosa|LAMB3-related_disorder|Amelogenesis_imperfecta_type_1A": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 1,
    "LAMB3-related_disorder": 6,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|not_provided": 2,
    "LAMB3-related_disorder|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "Junctional_epidermolysis_bullosa|not_provided|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Inborn_genetic_diseases": 7,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 25,
    "Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa|LAMB3-related_disorder": 1,
    "Junctional_epidermolysis_bullosa|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Junctional_epidermolysis_bullosa|LAMB3-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa": 2,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|Amelogenesis_imperfecta_type_1A|not_provided": 1,
    "Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Amelogenesis_imperfecta_type_1A|Inborn_genetic_diseases": 1,
    "not_provided|LAMB3-related_disorder|Junctional_epidermolysis_bullosa": 2,
    "Epidermolysis_bullosa": 2,
    "Amelogenesis_imperfecta_type_1A|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "not_specified|not_provided|Junctional_epidermolysis_bullosa|LAMB3-related_disorder": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "not_provided|Junctional_epidermolysis_bullosa|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "LAMB3-related_disorder|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa|LAMB3-related_disorder": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 40,
    "Inborn_genetic_diseases|LAMB3-related_disorder|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa|LAMB3-related_disorder": 2,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Amelogenesis_imperfecta_type_1A|not_specified": 1,
    "Junctional_epidermolysis_bullosa|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified": 1,
    "Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa|not_provided": 1,
    "Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|not_specified": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|not_specified|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "LAMB3-related_disorder|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "LAMB3-related_disorder|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A|not_provided": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Amelogenesis_imperfecta_type_1A|Junctional_epidermolysis_bullosa": 1,
    "HSD11B1-related_disorder": 1,
    "Cortisone_reductase_deficiency_2": 3,
    "not_provided|Cortisone_reductase_deficiency_2": 1,
    "Exstrophy-epispadias_complex": 6,
    "HSD11B1-related_disorder|not_specified|not_provided": 1,
    "Cortisone_reductase_deficiency_2|not_specified": 1,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 29,
    "Van_der_Woude_syndrome_1|Orofacial_cleft_6|_susceptibility_to": 17,
    "Orofacial_cleft_6|_susceptibility_to|not_provided|Van_der_Woude_syndrome_1": 3,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1|not_provided": 6,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Van_der_Woude_syndrome_1": 1,
    "not_provided|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 3,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1": 2,
    "Van_der_Woude_syndrome_1|Popliteal_pterygium_syndrome|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|not_provided": 5,
    "Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to": 9,
    "Orofacial_cleft_6|_susceptibility_to|Inborn_genetic_diseases|Van_der_Woude_syndrome_1": 1,
    "Van_der_Woude_syndrome_1|Autosomal_dominant_popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to": 1,
    "IRF6-related_condition": 15,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1|Popliteal_pterygium_syndrome": 2,
    "Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome": 18,
    "Popliteal_pterygium_syndrome": 6,
    "Van_der_Woude_syndrome_1": 22,
    "Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome": 41,
    "Inborn_genetic_diseases|Popliteal_pterygium_syndrome": 1,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to": 13,
    "not_provided|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome": 2,
    "not_provided|Van_der_Woude_syndrome_1|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome": 1,
    "Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Van_der_Woude_syndrome_1|Autosomal_dominant_popliteal_pterygium_syndrome|not_provided": 1,
    "Van_der_Woude_syndrome_1|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to": 2,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1": 1,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome": 8,
    "not_provided|Popliteal_pterygium_syndrome": 1,
    "Orofacial_cleft_10": 21,
    "IRF6-related_condition|Inborn_genetic_diseases": 1,
    "Van_der_Woude_syndrome_1|not_specified|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|not_provided": 1,
    "Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome": 5,
    "Orofacial_cleft_6|_susceptibility_to": 3,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1|Autosomal_dominant_popliteal_pterygium_syndrome": 1,
    "Inborn_genetic_diseases|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome": 1,
    "not_provided|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to": 1,
    "Van_der_Woude_syndrome_1|Popliteal_pterygium_syndrome": 1,
    "Inborn_genetic_diseases|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 1,
    "Van_der_Woude_syndrome_1|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to": 1,
    "IRF6-related_condition|not_provided": 1,
    "not_provided|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome": 2,
    "Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Van_der_Woude_syndrome_1": 1,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1|Autosomal_dominant_popliteal_pterygium_syndrome|not_provided": 1,
    "Autosomal_dominant_popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 2,
    "Van_der_Woude_syndrome_1|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|not_provided|not_specified": 1,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|IRF6-related_condition|not_specified": 1,
    "Orofacial_cleft_6|_susceptibility_to|not_specified|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1|not_provided": 1,
    "Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|IRF6-related_condition": 1,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|not_provided|Van_der_Woude_syndrome_1": 3,
    "IRF6-related_condition|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome": 1,
    "not_provided|not_specified|Autosomal_dominant_popliteal_pterygium_syndrome": 1,
    "Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|not_provided": 1,
    "Orofacial_cleft_10|Selective_tooth_agenesis": 2,
    "Van_der_Woude_syndrome_1|not_specified|Orofacial_cleft_6|_susceptibility_to|not_provided|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Autosomal_dominant_popliteal_pterygium_syndrome": 1,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|not_provided|IRF6-related_condition": 1,
    "Inborn_genetic_diseases|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to": 1,
    "Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 1,
    "Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|IRF6-related_condition": 1,
    "not_provided|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Autosomal_dominant_popliteal_pterygium_syndrome": 1,
    "IRF6-related_condition|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Autosomal_dominant_popliteal_pterygium_syndrome|not_provided": 1,
    "Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1": 2,
    "not_provided|Van_der_Woude_syndrome|Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to": 1,
    "not_provided|Autosomal_dominant_popliteal_pterygium_syndrome|IRF6-related_condition": 1,
    "Van_der_Woude_syndrome_1|not_provided|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Autosomal_dominant_popliteal_pterygium_syndrome|not_specified": 1,
    "IRF6-related_condition|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome": 1,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1": 1,
    "Popliteal_pterygium_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome|not_provided|Van_der_Woude_syndrome_1|IRF6-related_condition": 1,
    "not_provided|Cleft_palate|IRF6-related_condition|Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome_1": 1,
    "Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 1,
    "IRF6-related_condition|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1": 1,
    "Orofacial_cleft_6|_susceptibility_to|not_provided|not_specified|Van_der_Woude_syndrome_1": 1,
    "not_provided|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Orofacial_cleft_6|_susceptibility_to|Van_der_Woude_syndrome_1|not_specified": 1,
    "not_provided|Orofacial_cleft_6|_susceptibility_to": 1,
    "Van_der_Woude_syndrome_1|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 2,
    "not_provided|Van_der_Woude_syndrome_1|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "Orofacial_cleft_6|_susceptibility_to|Popliteal_pterygium_syndrome|Van_der_Woude_syndrome|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Van_der_Woude_syndrome_1|not_provided": 1,
    "not_specified|SYT14-related_disorder": 1,
    "SYT14-related_disorder": 2,
    "SYT14-related_disorder|not_provided": 2,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_11|not_specified": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_11": 2,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_11": 2,
    "not_provided|not_specified|SYT14-related_disorder": 1,
    "HHAT-related_disorder": 3,
    "HHAT-related_disorder|not_provided": 6,
    "Chondrodysplasia-pseudohermaphroditism_syndrome": 6,
    "not_provided|HHAT-related_disorder": 2,
    "not_provided|Thalidomide_response": 1,
    "Chondrodysplasia-pseudohermaphroditism_syndrome|not_provided|HHAT-related_disorder": 1,
    "not_provided|KCNH1-related_disorder": 14,
    "not_provided|Temple-Baraitser_syndrome|Zimmermann-Laband_syndrome_1": 1,
    "Zimmermann-Laband_syndrome_1": 11,
    "Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|KCNH1-related_disorder": 1,
    "KCNH1-related_disorder|not_provided|Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome": 1,
    "Temple-Baraitser_syndrome": 9,
    "KCNH1_associated_disorder|not_provided": 3,
    "KCNH1-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|KCNH1-related_disorder|not_provided": 1,
    "KCNH1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome|not_provided": 1,
    "Zimmermann-Laband_syndrome_1|not_provided": 1,
    "not_provided|KCNH1-related_disorder|Inborn_genetic_diseases": 1,
    "Temple-Baraitser_syndrome|Zimmermann-Laband_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "KCNH1-related_disorder": 12,
    "Temple-Baraitser_syndrome|Zimmermann-Laband_syndrome_1": 2,
    "KCNH1-related_disorder|Inborn_genetic_diseases|not_provided|Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome": 1,
    "Temple-Baraitser_syndrome|Zimmermann-Laband_syndrome_1|not_provided": 1,
    "not_provided|Temple-Baraitser_syndrome": 2,
    "not_provided|Zimmermann-Laband_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome|See_cases": 1,
    "KCNH1-related_neurodevelopmental_disorder_with_multiple_anomalies": 1,
    "Inborn_genetic_diseases|KCNH1-related_disorder|Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome|not_provided|Intellectual_disability|_severe|Abnormal_facial_shape|Seizure|Intellectual_disability": 1,
    "Temple-Baraitser_syndrome|not_provided": 1,
    "Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome": 1,
    "KCNH1-related_phenotype": 1,
    "not_provided|Epilepsy": 23,
    "not_specified|not_provided|Zimmermann-Laband_syndrome_1|Temple-Baraitser_syndrome": 1,
    "not_provided|Temple-Baraitser_syndrome|Zimmermann-Laband_syndrome_1|not_specified": 1,
    "Leber_congenital_amaurosis_12|not_provided": 14,
    "Leber_congenital_amaurosis_12": 184,
    "not_provided|Leber_congenital_amaurosis_12": 7,
    "not_provided|not_specified|Leber_congenital_amaurosis_12": 2,
    "not_provided|Leber_congenital_amaurosis_12|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_specified|Leber_congenital_amaurosis_12": 1,
    "RD3-related_disorder|Leber_congenital_amaurosis_12|not_provided": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_12": 3,
    "Leber_congenital_amaurosis_12|RD3-related_disorder": 3,
    "Leber_congenital_amaurosis_12|not_specified|not_provided": 1,
    "Leber_congenital_amaurosis_12|Inborn_genetic_diseases": 3,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_12": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_12": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_12|Abnormality_of_the_eye|RD3-related_disorder": 1,
    "not_provided|Leber_congenital_amaurosis_12|not_specified": 1,
    "NEK2-related_disorder": 1,
    "NEK2-related_disorder|not_provided": 2,
    "NEK2-related_disorder|Retinitis_pigmentosa_67|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_67": 1,
    "Retinitis_pigmentosa_67": 1,
    "not_provided|Retinitis_pigmentosa_67|Retinal_dystrophy|not_specified": 1,
    "NEK2-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_67|not_provided": 1,
    "INTS7-related_disorder": 2,
    "ATF3-related_disorder": 2,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 139,
    "not_provided|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 41,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|not_provided": 17,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|not_provided": 2,
    "Jeune_thoracic_dystrophy": 2646,
    "not_provided|FLVCR1-related_disorder": 3,
    "not_provided|not_specified|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 3,
    "Inborn_genetic_diseases|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 5,
    "Sensory_neuropathy|Abnormal_retinal_morphology": 1,
    "Inborn_genetic_diseases|not_provided|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "FLVCR1-related_disorder|not_provided": 2,
    "Hereditary_sensory_and_autonomic_neuropathy|Retinitis_pigmentosa|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "not_specified|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|FLVCR1-related_disorder|not_provided": 1,
    "Short_rib-polydactyly_syndrome": 3,
    "Retinal_dystrophy|FLVCR1-related_disorder|not_provided": 1,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 3,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|Neurodevelopmental_disorder_with_microcephaly|_absent_speech|_and_hypotonia|not_provided": 1,
    "not_specified|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|not_provided": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|FLVCR1-related_disorder|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_absent_speech|_and_hypotonia|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_absent_speech|_and_hypotonia": 3,
    "FLVCR1-related_disorder|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|not_provided": 1,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|Retinal_dystrophy|not_provided": 1,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|Neurodevelopmental_disorder_with_microcephaly|_absent_speech|_and_hypotonia": 1,
    "not_provided|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|not_specified": 2,
    "not_specified|FLVCR1-related_disorder|not_provided": 1,
    "FLVCR1-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "Hypotonia|Abnormal_cerebral_white_matter_morphology|Hypoplasia_of_the_corpus_callosum|Delayed_myelination|Global_developmental_delay|Periventricular_leukomalacia": 1,
    "PROX1-related_disorder": 6,
    "Lymphedema-posterior_choanal_atresia_syndrome": 15,
    "not_provided|Lymphedema-posterior_choanal_atresia_syndrome": 6,
    "not_specified|Lymphedema-posterior_choanal_atresia_syndrome": 2,
    "Lymphedema-posterior_choanal_atresia_syndrome|not_specified": 2,
    "Lymphedema-posterior_choanal_atresia_syndrome|not_provided": 1,
    "not_provided|PTPN14-related_disorder": 1,
    "PTPN14-related_disorder|not_provided": 3,
    "PTPN14-related_disorder": 7,
    "Stromme_syndrome": 42,
    "not_provided|Stromme_syndrome": 28,
    "CENPF-related_disorder": 32,
    "Stromme_syndrome|not_provided": 12,
    "not_specified|not_provided|CENPF-related_disorder": 2,
    "CENPF-related_disorder|Stromme_syndrome": 1,
    "not_provided|CENPF-related_disorder": 3,
    "Cystinuria": 513,
    "CENPF-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Stromme_syndrome": 1,
    "CENPF-related_disorder|not_provided": 10,
    "CENPF-related_disorder|not_provided|not_specified": 1,
    "CENPF-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "CENPF-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|CENPF-related_disorder": 1,
    "Stromme_syndrome|Inborn_genetic_diseases": 2,
    "Stromme_syndrome|not_specified": 2,
    "not_provided|not_specified|CENPF-related_disorder": 1,
    "not_specified|not_provided|Stromme_syndrome": 1,
    "CENPF-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|CENPF-related_disorder|not_specified": 1,
    "not_provided|Stromme_syndrome|CENPF-related_disorder": 1,
    "Stromme_syndrome|Neurodevelopmental_delay": 1,
    "not_provided|CENPF-related_disorder|Stromme_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|CENPF-related_disorder": 1,
    "Inborn_genetic_diseases|Stromme_syndrome|not_provided": 1,
    "not_specified|CENPF-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|CENPF-related_disorder|Inborn_genetic_diseases": 1,
    "CENPF-related_disorder|not_specified": 1,
    "Primary_ciliary_dyskinesia_29": 11,
    "not_specified|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 15,
    "Inborn_genetic_diseases|KCTD3-related_disorder": 1,
    "KCTD3-related_disorder": 3,
    "Autism|_susceptibility_to|_15": 3,
    "Autism|_susceptibility_to|_15|Congenital_cerebellar_hypoplasia|Severe_global_developmental_delay|Seizure": 1,
    "Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39|not_provided": 10,
    "Usher_syndrome_type_2A|not_provided": 168,
    "Inborn_genetic_diseases|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 3,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 86,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 54,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 58,
    "Retinitis_pigmentosa_39": 186,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A|not_provided": 6,
    "not_specified|Usher_syndrome_type_2A|not_provided|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 96,
    "not_specified|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 30,
    "Usher_syndrome_type_2A": 496,
    "not_specified|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A": 4,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided": 10,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided": 22,
    "Usher_syndrome|USH2A-related_disorder|not_provided": 2,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases|not_provided": 4,
    "Retinitis_pigmentosa_39|not_provided|not_specified": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_specified|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 14,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|not_specified": 2,
    "not_provided|Retinitis_pigmentosa_39": 54,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 15,
    "not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 12,
    "USH2A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 15,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided": 2,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 4,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 5,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 90,
    "not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "not_provided|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39": 6,
    "Retinitis_pigmentosa_39|Usher_syndrome": 1,
    "not_specified|not_provided|Usher_syndrome": 3,
    "not_provided|Usher_syndrome_type_2A": 163,
    "not_provided|USH2A-related_disorder": 7,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome|not_provided|Retinal_dystrophy": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 14,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 4,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 58,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 4,
    "USH2A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 9,
    "not_provided|not_specified|Retinitis_pigmentosa": 8,
    "Usher_syndrome_type_2A|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 8,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified": 3,
    "Usher_syndrome_type_2A|USH2A-related_disorder|not_provided|Retinitis_pigmentosa_39|not_specified": 2,
    "not_provided|Usher_syndrome_type_2A|Retinal_dystrophy": 3,
    "Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2|Usher_syndrome_type_2A": 1,
    "not_specified|Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 4,
    "Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A": 27,
    "not_specified|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|Usher_syndrome_type_2A|not_specified": 4,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|Retinal_dystrophy": 2,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases": 3,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "Usher_syndrome": 92,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_39|not_provided": 67,
    "Usher_syndrome|Usher_syndrome_type_2A": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided": 4,
    "Usher_syndrome_type_2A|not_provided|not_specified|Retinitis_pigmentosa_39": 13,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 10,
    "Rare_genetic_deafness|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 5,
    "Retinitis_pigmentosa_39|not_specified|not_provided|Usher_syndrome_type_2A": 2,
    "not_provided|Usher_syndrome|Usher_syndrome_type_2A": 2,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|Retinal_dystrophy|not_provided": 1,
    "USH2A-related_disorder|not_provided": 15,
    "Rare_genetic_deafness|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|Retinal_dystrophy": 6,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 3,
    "Usher_syndrome_type_2|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified": 7,
    "Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2A": 6,
    "Retinitis_pigmentosa_39|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2A": 2,
    "not_provided|not_specified|Usher_syndrome_type_2A": 4,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2A|not_specified": 1,
    "Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa": 3,
    "Retinal_dystrophy|Usher_syndrome_type_2A": 5,
    "not_specified|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|USH2A-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39": 3,
    "not_specified|not_provided|Retinitis_pigmentosa_39|Retinitis_pigmentosa|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_specified|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_specified|not_provided": 3,
    "Hearing_impairment|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified": 17,
    "Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Monogenic_hearing_loss|Usher_syndrome|Retinal_dystrophy|USH2A-related_disorder": 1,
    "Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "Usher_syndrome_type_2|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "not_provided|not_specified|Usher_syndrome": 2,
    "Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided": 1,
    "Usher_syndrome_type_2A|not_specified": 4,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|not_specified|Inborn_genetic_diseases": 1,
    "USH2A-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 2,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|not_specified": 7,
    "not_specified|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39": 8,
    "not_provided|not_specified|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|Rare_genetic_deafness": 1,
    "Usher_syndrome|USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Rare_genetic_deafness": 1,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_2A": 3,
    "Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_degeneration|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 4,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder": 21,
    "Usher_syndrome|not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2|not_provided": 16,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified": 8,
    "not_specified|USH2A-related_disorder|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 2,
    "not_specified|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 2,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy": 3,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 3,
    "not_provided|Hypoplasia_of_the_brainstem|Amblyopia|Joubert_syndrome|Congenital_cerebellar_hypoplasia|Cerebellar_hemisphere_hypoplasia|Delayed_speech_and_language_development|Motor_delay|Congenital_sensorineural_hearing_impairment|not_specified": 1,
    "Usher_syndrome_type_2": 24,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39": 2,
    "Retinal_dystrophy|not_provided|USH2A-related_disorder|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36": 8,
    "not_provided|Usher_syndrome_type_2A|Inborn_genetic_diseases": 4,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|not_specified": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome|not_provided": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|Usher_syndrome": 1,
    "Ear_malformation": 23,
    "USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy": 1,
    "not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 2,
    "not_provided|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 2,
    "not_specified|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 1,
    "USH2A-related_disorder|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_specified": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39": 7,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Usher_syndrome_type_2A": 4,
    "Usher_syndrome_type_2A|not_specified|not_provided": 6,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome": 2,
    "not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2A": 3,
    "Usher_syndrome|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 3,
    "Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|Inborn_genetic_diseases": 5,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided": 11,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|USH2A-related_disorder|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|Rare_genetic_deafness": 1,
    "Retinitis_pigmentosa_39|not_provided|Childhood_onset_hearing_loss|not_specified|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 3,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 2,
    "Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 2,
    "not_provided|Rare_genetic_deafness|Retinitis_pigmentosa_39|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_specified": 2,
    "Retinitis_pigmentosa_39|not_specified": 1,
    "Retinitis_pigmentosa_39|Retinitis_pigmentosa|Usher_syndrome|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 2,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Usher_syndrome": 2,
    "not_specified|Usher_syndrome_type_2A": 4,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases|not_provided|USH2A-related_disorder": 1,
    "Rare_genetic_deafness|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|Inborn_genetic_diseases": 4,
    "Rare_genetic_deafness|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Usher_syndrome_type_2": 7,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39": 13,
    "not_provided|USH2A-related_disorder|Usher_syndrome_type_2A": 3,
    "Usher_syndrome|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 2,
    "not_provided|Usher_syndrome_type_2A|Retinal_dystrophy|USH2A-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "not_specified|Usher_syndrome_type_2A|not_provided": 4,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|Rare_genetic_deafness|not_provided": 2,
    "Usher_syndrome_type_2|Retinitis_pigmentosa_39": 2,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome|Usher_syndrome_type_2A": 3,
    "not_provided|Retinitis_pigmentosa_39|not_specified|Usher_syndrome_type_2A": 6,
    "Usher_syndrome_type_2A|Retinal_dystrophy|Retinitis_pigmentosa_39|USH2A-related_disorder|not_provided": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|Usher_syndrome|not_provided|Retinal_dystrophy": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_2A|not_provided": 3,
    "Usher_syndrome_type_2A|not_provided|USH2A-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|not_provided": 10,
    "Rare_genetic_deafness|Usher_syndrome|Retinitis_pigmentosa_39": 2,
    "not_specified|Inborn_genetic_diseases|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 2,
    "Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|not_specified": 1,
    "not_specified|Usher_syndrome_type_2A|Inborn_genetic_diseases|USH2A-related_disorder|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy": 7,
    "not_specified|not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2A": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 7,
    "USH2A-related_disorder|Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|not_specified|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa_39|not_specified|Usher_syndrome_type_2A|not_provided": 4,
    "Usher_syndrome_type_2A|USH2A-related_disorder|not_provided|Retinal_dystrophy|not_specified": 1,
    "Usher_syndrome|USH2A-related_disorder|Retinal_dystrophy|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Hearing_impairment|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A": 4,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 4,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39": 1,
    "not_provided|Usher_syndrome_type_2A|Inborn_genetic_diseases|Retinitis_pigmentosa_39|Retinal_dystrophy|not_specified": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|Retinal_dystrophy|not_provided": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 5,
    "Retinal_dystrophy|not_provided|Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2A": 4,
    "Retinal_dystrophy|Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "USH2A-related_disorder|not_provided|not_specified|Usher_syndrome_type_2A": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 4,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Inborn_genetic_diseases": 5,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|USH2A-related_disorder": 2,
    "USH2A-related_disorder|Usher_syndrome|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|not_provided": 21,
    "not_provided|not_specified|Retinitis_pigmentosa_39": 2,
    "Retinitis_pigmentosa_39|Inborn_genetic_diseases|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 1,
    "Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Rare_genetic_deafness|not_provided|Usher_syndrome_type_2|USH2A-related_disorder|Retinal_dystrophy": 1,
    "USH2A-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|USH2A-related_disorder|not_specified|not_provided": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided|Rare_genetic_deafness": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2|USH2A-related_disorder|Usher_syndrome_type_3A|Rare_genetic_deafness|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|Congenital_sensorineural_hearing_impairment|Hearing_impairment|See_cases": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|not_specified": 12,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|not_provided": 4,
    "not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 10,
    "not_provided|Usher_syndrome_type_2A|Inborn_genetic_diseases|not_specified": 1,
    "Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome": 4,
    "not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A": 7,
    "Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39": 1,
    "not_specified|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39": 1,
    "not_specified|not_provided|Usher_syndrome_type_2A": 7,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|Inborn_genetic_diseases": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 3,
    "USH2A-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Usher_syndrome_type_2A|not_specified|not_provided": 1,
    "Usher_syndrome_type_2A|not_provided|Retinal_dystrophy": 3,
    "Retinitis_pigmentosa|Rare_genetic_deafness|not_provided|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|not_provided|not_specified": 6,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Rare_genetic_deafness|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 2,
    "not_provided|Usher_syndrome": 17,
    "not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy": 3,
    "Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases": 7,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|not_specified|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Rare_genetic_deafness|Usher_syndrome": 1,
    "not_provided|Usher_syndrome_type_2|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|not_provided|not_specified": 3,
    "not_provided|Usher_syndrome_type_2A|USH2A-related_disorder|not_specified": 2,
    "Usher_syndrome|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 2,
    "not_provided|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "not_provided|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 2,
    "not_provided|Retinal_dystrophy|Usher_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 5,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa_39": 9,
    "Usher_syndrome_type_2|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_2A": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome": 4,
    "Usher_syndrome_type_2A|Retinal_dystrophy": 3,
    "not_provided|Congenital_stationary_night_blindness": 9,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Rare_genetic_deafness|not_provided": 1,
    "USH2A-related_disorder|Usher_syndrome_type_2A|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|not_provided": 2,
    "Rare_genetic_deafness|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|not_specified|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_39": 2,
    "not_provided|Cone-rod_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|not_provided|not_specified|Retinal_dystrophy|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Rare_genetic_deafness|Usher_syndrome|USH2A-related_disorder|See_cases|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa": 19,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|not_specified": 5,
    "Usher_syndrome_type_2A|USH2A-related_disorder|not_specified|not_provided|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|USH2A-related_disorder|Retinal_dystrophy": 2,
    "Usher_syndrome_type_2A|not_provided|USH2A-related_disorder|not_specified|Retinitis_pigmentosa_39": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A": 1,
    "not_provided|Retinitis_pigmentosa_39|Inborn_genetic_diseases|Usher_syndrome_type_2A": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 4,
    "not_specified|Retinal_dystrophy|not_provided|Usher_syndrome_type_2A": 3,
    "not_provided|Retinitis_pigmentosa_39|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|Rare_genetic_deafness|Retinal_dystrophy": 1,
    "not_provided|USH2A-related_disorder|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa_39|not_specified": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|not_provided": 2,
    "Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|Hearing_impairment": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_specified|not_provided": 3,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_39|Inborn_genetic_diseases|not_provided|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa": 3,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|USH2A-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Usher_syndrome|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "USH2A-related_disorder|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Usher_syndrome_type_1|Retinitis_pigmentosa": 1,
    "not_provided|Usher_syndrome_type_2A|Usher_syndrome": 4,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2|not_provided": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|Retinitis_pigmentosa_39|not_specified|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinal_disorders|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|not_provided|not_specified|Retinitis_pigmentosa_39|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_specified": 3,
    "Retinal_dystrophy|Usher_syndrome_type_2A|not_provided": 2,
    "Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome|not_provided": 1,
    "not_provided|Cone-rod_dystrophy|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 4,
    "Usher_syndrome_type_2A|Usher_syndrome": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Rare_genetic_deafness|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|USH2A-related_disorder": 6,
    "Usher_syndrome|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39": 1,
    "not_specified|Inborn_genetic_diseases|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome_type_2A|Nonsyndromic_genetic_hearing_loss": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|not_specified": 1,
    "not_specified|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases|not_provided": 5,
    "not_provided|Retinal_dystrophy|not_specified|Usher_syndrome_type_2A": 1,
    "Retinitis_pigmentosa_39|not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa|not_provided": 1,
    "Rare_genetic_deafness|not_provided|USH2A-related_disorder|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified": 3,
    "Usher_syndrome|not_provided|Usher_syndrome_type_2A": 3,
    "Usher_syndrome|Rare_genetic_deafness|Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa_39|not_provided": 1,
    "not_provided|Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|Usher_syndrome|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2|USH2A-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Hearing_impairment|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_39|Retinitis_pigmentosa|not_provided|Usher_syndrome_type_2A": 1,
    "Rare_genetic_deafness|Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|not_provided|not_specified|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_specified|Retinitis_pigmentosa_39|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_39|Rare_genetic_deafness": 1,
    "Usher_syndrome_type_2A|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_39": 2,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases|USH2A-related_disorder": 1,
    "See_cases|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|not_provided|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified": 1,
    "Optic_atrophy|not_provided|Usher_syndrome_type_2A": 1,
    "not_specified|not_provided|Usher_syndrome_type_2A|USH2A-related_disorder|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|not_provided|not_specified|Retinitis_pigmentosa_39": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 2,
    "Hearing_loss|USH2A-related_disorder": 1,
    "not_provided|Usher_syndrome_type_2A|Inborn_genetic_diseases|Retinitis_pigmentosa_39": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2A": 6,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|Rare_genetic_deafness|Retinitis_pigmentosa|Usher_syndrome|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|not_specified|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|USH2A-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy": 8,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 3,
    "Rare_genetic_deafness|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 3,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Hearing_impairment": 3,
    "Usher_syndrome|USH2A-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Rare_genetic_deafness|Usher_syndrome|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa_39": 1,
    "Rare_genetic_deafness|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|not_specified": 7,
    "Usher_syndrome_type_2|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Retinal_dystrophy|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa_39|not_provided|not_specified|Usher_syndrome_type_2A": 1,
    "not_provided|not_specified|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided|Usher_syndrome|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome|Retinitis_pigmentosa": 1,
    "not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|See_cases": 1,
    "Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Usher_syndrome_type_2": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy": 2,
    "Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome": 2,
    "Usher_syndrome_type_2A|not_provided|Usher_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2|Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "Inborn_genetic_diseases|not_provided|USH2A-related_disorder|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_39|not_specified": 1,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|USH2A-related_disorder|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome|Retinitis_pigmentosa|Usher_syndrome_type_2|Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|USH2A-related_disorder": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|USH2A-related_disorder": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Rare_genetic_deafness|not_provided|Usher_syndrome_type_2A|Retinal_dystrophy": 1,
    "Ear_malformation|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified": 1,
    "not_provided|Retinal_dystrophy|USH2A-related_disorder|Usher_syndrome_type_2A": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|not_specified|Retinitis_pigmentosa_39": 1,
    "not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A": 3,
    "not_provided|Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "not_provided|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "Rare_genetic_deafness|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinal_dystrophy|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Leber_congenital_amaurosis|not_specified": 1,
    "USH2A-related_disorder|not_provided|Usher_syndrome_type_2A|not_specified": 1,
    "not_provided|Usher_syndrome_type_2|Usher_syndrome_type_2A": 3,
    "not_provided|USH2A-related_disorder|Usher_syndrome": 2,
    "Retinal_dystrophy|Usher_syndrome|USH2A-related_disorder|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|Cone-rod_dystrophy_3": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|USH2A-related_disorder|Retinal_dystrophy|not_specified": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_39|USH2A-related_disorder|Usher_syndrome_type_2A": 1,
    "Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 1,
    "Usher_syndrome|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Congenital_sensorineural_hearing_impairment": 1,
    "USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_specified|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39|Usher_syndrome": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|USH2A-related_disorder": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|not_provided|Retinitis_pigmentosa_39": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Usher_syndrome|Usher_syndrome_type_2A": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|Retinitis_pigmentosa_39|not_provided": 1,
    "not_provided|USH2A-related_disorder|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 2,
    "Usher_syndrome_type_2A|Inborn_genetic_diseases|USH2A-related_disorder|not_provided|not_specified": 1,
    "not_specified|USH2A-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_specified|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Rare_genetic_deafness|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "Usher_syndrome|not_specified|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "Rare_genetic_deafness|not_provided|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "not_provided|USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa|not_provided": 1,
    "USH2A-related_disorder|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases": 4,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|not_provided|Progressive_cone_dystrophy_(without_rod_involvement)|USH2A-related_disorder": 1,
    "USH2A-related_disorder|not_provided|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|USH2A-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2|Rare_genetic_deafness|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|USH2A-related_disorder|Retinal_dystrophy": 1,
    "Rare_genetic_deafness|USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Rare_genetic_deafness|USH2A-related_disorder|Usher_syndrome|Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|USH2A-related_disorder|not_provided": 1,
    "Usher_syndrome_type_2|Usher_syndrome_type_2A|not_provided": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_2|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "USH2A-related_disorder|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Childhood_onset_hearing_loss|not_provided": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided": 1,
    "Rare_genetic_deafness|USH2A-related_disorder|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_2A": 2,
    "Retinal_dystrophy|USH2A-related_disorder|Retinitis_pigmentosa_39|not_provided": 1,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 3,
    "Usher_syndrome_type_2A|Monogenic_hearing_loss": 1,
    "not_provided|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 2,
    "Usher_syndrome|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa|not_provided|not_specified": 2,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|Retinal_dystrophy|USH2A-related_disorder|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_specified": 3,
    "Retinitis_pigmentosa_39|USH2A-related_disorder|not_provided|Usher_syndrome_type_2A|not_specified": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Hearing_impairment|Retinal_dystrophy": 1,
    "not_specified|Retinal_dystrophy|not_provided|USH2A-related_disorder|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|not_specified|not_provided|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Usher_syndrome|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|Rare_genetic_deafness": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Sensorineural_hearing_loss_disorder|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_39|not_specified": 1,
    "Retinal_dystrophy|not_provided|USH2A-related_disorder|not_specified|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome": 1,
    "Usher_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Inborn_genetic_diseases|Retinitis_pigmentosa_39|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Rare_genetic_deafness|USH2A-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa-deafness_syndrome|Retinitis_Pigmentosa|_Recessive": 3,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A": 29,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa": 14,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 2,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa|not_provided": 2,
    "Retinitis_pigmentosa|not_provided|Usher_syndrome_type_2A": 4,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|not_provided": 5,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|USH2A-related_disorder|Retinitis_pigmentosa": 1,
    "Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39": 1,
    "not_specified|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa_39": 1,
    "not_provided|Retinitis_pigmentosa_39|not_specified|Inborn_genetic_diseases|Usher_syndrome_type_2A": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Usher_syndrome_type_2A|Usher_syndrome|Rare_genetic_deafness": 1,
    "Usher_syndrome_type_2A|not_specified|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases|Usher_syndrome_type_2A": 1,
    "not_provided|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_39": 1,
    "Inborn_genetic_diseases|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome|USH2A-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|not_specified|Usher_syndrome|USH2A-related_disorder": 1,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39|not_specified": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|Usher_syndrome|not_provided|USH2A-related_disorder": 1,
    "Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases|not_specified|Retinitis_pigmentosa_39": 1,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|USH2A-related_disorder": 1,
    "Retinitis_pigmentosa-deafness_syndrome|Retinitis_Pigmentosa|_Recessive|not_specified|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa-deafness_syndrome|Retinitis_pigmentosa_39|Retinitis_Pigmentosa|_Recessive|not_specified": 1,
    "Retinitis_pigmentosa_39|USH2A-related_disorder|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|not_specified": 1,
    "Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|not_specified|Retinitis_pigmentosa": 1,
    "not_provided|Usher_syndrome_type_2A|Rare_genetic_deafness|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Retinitis_pigmentosa": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|not_provided": 2,
    "Usher_syndrome|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa_39|Usher_syndrome|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|USH2A-related_disorder|not_provided": 1,
    "Usher_syndrome_type_2A|Usher_syndrome_type_2|Retinitis_pigmentosa_39|not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|Retinitis_pigmentosa_39|not_specified|Usher_syndrome_type_1|USH2A-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|See_cases|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinal_dystrophy": 1,
    "not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive|Usher_syndrome|Deafness": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|Usher_syndrome_type_2A": 2,
    "not_specified|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|Retinitis_pigmentosa|not_specified": 1,
    "Usher_syndrome_type_2A|Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_2A": 1,
    "Rare_genetic_deafness|Usher_syndrome|not_provided": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_39|not_provided|not_specified|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|USH2A-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2|not_provided|Usher_syndrome_type_2A": 3,
    "Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa": 1,
    "USH2A-related_disorder|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa-deafness_syndrome|not_provided": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_39|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Retinitis_pigmentosa|not_specified": 1,
    "not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_39|not_provided": 1,
    "not_provided|Rare_genetic_deafness|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2|Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome_type_2": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|not_specified": 2,
    "Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome|Rare_genetic_deafness|Retinal_dystrophy": 1,
    "not_specified|not_provided|Usher_syndrome_type_2A|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Hearing_impairment|Usher_syndrome_type_2A|not_provided|Usher_syndrome|Progressive_cone_dystrophy_(without_rod_involvement)|not_specified|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis|Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Rare_genetic_deafness|Usher_syndrome|Usher_syndrome_type_2|USH2A-related_disorder|Macular_dystrophy|Congenital_stationary_night_blindness|Retinal_dystrophy|Inborn_genetic_diseases|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|USH2A-related_disorder|not_provided|Retinitis_pigmentosa|Usher_syndrome": 1,
    "USH2A-related_disorder|Usher_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa|See_cases|Ear_malformation": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy|not_provided": 2,
    "Usher_syndrome_type_2|Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "Hearing_impairment|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|Usher_syndrome_type_2A|not_specified": 1,
    "Usher_syndrome|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|USH2A-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "USH2A-related_disorder|Usher_syndrome_type_2|Retinitis_pigmentosa_39|not_provided": 1,
    "Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_39": 2,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|not_specified|Usher_syndrome_type_2A|not_provided": 1,
    "not_specified|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "USH2A-related_disorder|Hearing_impairment|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_39|Rare_genetic_deafness|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome|Usher_syndrome_type_2A|Joubert_syndrome|Congenital_cerebellar_hypoplasia|Cerebellar_hemisphere_hypoplasia|Congenital_sensorineural_hearing_impairment|Hypoplasia_of_the_brainstem|Amblyopia|Delayed_speech_and_language_development|Motor_delay|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_39": 1,
    "not_provided|Leber_congenital_amaurosis|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified": 1,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|not_specified|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39|not_specified": 1,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Hearing_impairment": 1,
    "Usher_syndrome|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|Ear_malformation": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|USH2A-related_disorder|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|Rare_genetic_deafness|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|USH2A-related_disorder|Nonsyndromic_genetic_hearing_loss": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome_type_2": 1,
    "Retinal_dystrophy|not_specified|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome_type_2A|Inborn_genetic_diseases|Retinitis_pigmentosa_39|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|not_provided|Usher_syndrome": 1,
    "Retinitis_pigmentosa-deafness_syndrome|not_provided|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_39|not_specified|Usher_syndrome_type_2A": 1,
    "Retinal_disorders|Monogenic_hearing_loss|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A": 3,
    "Rare_genetic_deafness|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Usher_syndrome": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinitis_pigmentosa|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa_39|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided|Usher_syndrome": 1,
    "Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy|not_provided": 1,
    "Hearing_impairment|not_provided": 36,
    "Rare_genetic_deafness|Usher_syndrome|USH2A-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa": 1,
    "Rare_genetic_deafness|USH2A-related_disorder|Cone-rod_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome_type_2|not_specified|Retinitis_pigmentosa_39|not_provided": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "Usher_syndrome|not_provided|Rare_genetic_deafness|USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 1,
    "Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_2|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_specified|USH2A-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Usher_syndrome_type_2A|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome|not_provided|Rare_genetic_deafness|Retinal_dystrophy": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa|Retinitis_pigmentosa_39": 1,
    "Pigmentary_retinopathy|Blindness|Rod-cone_dystrophy|Abnormal_macular_morphology|Retinal_pigment_epithelial_atrophy|Usher_syndrome_type_2|Rare_genetic_deafness|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|not_provided": 1,
    "Rare_genetic_deafness|Retinal_dystrophy|Retinal_degeneration|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39|Usher_syndrome|Retinitis_pigmentosa": 1,
    "USH2A-related_disorder|Usher_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|not_provided|Hearing_impairment": 1,
    "Retinitis_pigmentosa_39|Usher_syndrome|Usher_syndrome_type_2A|not_provided": 1,
    "Usher_syndrome_type_2A|Retinal_dystrophy|Retinitis_pigmentosa|not_specified|not_provided": 2,
    "not_provided|not_specified|Usher_syndrome_type_2A|Retinal_dystrophy|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy|not_provided|Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A": 1,
    "Usher_syndrome|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy|Rare_genetic_deafness|not_provided": 1,
    "Usher_syndrome_type_2|Usher_syndrome|Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|not_provided": 1,
    "Usher_syndrome_type_2|Retinitis_pigmentosa_39|not_provided|Usher_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinal_dystrophy": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_2A|Retinal_dystrophy|Retinitis_pigmentosa_39|Usher_syndrome|USH2A-related_disorder|Retinitis_pigmentosa|not_provided": 1,
    "Usher_syndrome_type_2A|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_39|Retinal_dystrophy|not_specified": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Usher_syndrome_type_2A|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "USH2A-related_disorder|not_provided|not_specified|Retinitis_pigmentosa|Usher_syndrome_type_2A": 1,
    "USH2A-related_disorder|Retinitis_pigmentosa|not_provided|Usher_syndrome_type_2A|not_specified": 1,
    "Retinal_dystrophy|Usher_syndrome_type_2A|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2A|not_provided|Retinitis_pigmentosa_39": 1,
    "Usher_syndrome|USH2A-related_disorder|Retinitis_pigmentosa_39|Usher_syndrome_type_2|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_2A|not_specified|Retinitis_pigmentosa_39": 1,
    "not_provided|Retinitis_pigmentosa_39|Usher_syndrome_type_2A|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_2A|Usher_syndrome|not_provided|Retinitis_pigmentosa_39|Retinitis_pigmentosa": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_39|Retinal_dystrophy": 1,
    "not_provided|Usher_syndrome_type_2A|Retinitis_pigmentosa_39|Usher_syndrome": 1,
    "not_provided|Loeys-Dietz_syndrome_4": 36,
    "Loeys-Dietz_syndrome_4|Loeys-Dietz_syndrome": 3,
    "Loeys-Dietz_syndrome_4": 327,
    "Loeys-Dietz_syndrome": 75,
    "not_provided|Loeys-Dietz_syndrome": 5,
    "not_provided|Loeys-Dietz_syndrome_4|Loeys-Dietz_syndrome": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Loeys-Dietz_syndrome_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4": 32,
    "Loeys-Dietz_syndrome_4|TGFB2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_4|not_provided": 9,
    "not_specified|Loeys-Dietz_syndrome_4": 3,
    "Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 32,
    "TGFB2-related_disorder": 6,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_4": 2,
    "TGFB2-related_disorder|Loeys-Dietz_syndrome_4": 2,
    "Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "not_specified|Ehlers-Danlos_syndrome|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_aortopathy": 13,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_4": 5,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hirschsprung_disease|_susceptibility_to|_1|Holt-Oram_syndrome": 1,
    "Loeys-Dietz_syndrome_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4|not_provided": 1,
    "not_provided|not_specified|Loeys-Dietz_syndrome_4": 2,
    "TGFB2-related_disorder|Aortic_aneurysm|not_specified|Ehlers-Danlos_syndrome|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Proteinuria": 1,
    "Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "TGFB2-related_disorder|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Loeys-Dietz_syndrome_4|not_specified": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB2-related_disorder": 1,
    "Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 4,
    "Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_4": 1,
    "not_provided|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_4": 1,
    "Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Loeys-Dietz_syndrome_4|not_provided|Loeys-Dietz_syndrome": 2,
    "Ehlers-Danlos_syndrome|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Loeys-Dietz_syndrome_4|not_provided|TGFB2-related_disorder|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Holt-Oram_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|not_provided|Loeys-Dietz_syndrome_4": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4|not_provided": 2,
    "TGFB2-related_disorder|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB2-related_disorder|Loeys-Dietz_syndrome_4": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_4": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4": 1,
    "Loeys-Dietz_syndrome_4|not_provided|TGFB2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFB2-related_disorder|not_provided|Familial_aortopathy|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic|_TGFB2_related|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Loeys-Dietz_syndrome_4|not_specified": 1,
    "not_provided|Loeys-Dietz_syndrome_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB2-related_disorder": 1,
    "not_provided|Loeys-Dietz_syndrome_4|TGFB2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "Loeys-Dietz_syndrome_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Atrial_septal_defect_1": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_4|not_specified": 1,
    "not_provided|Familial_aortopathy": 1,
    "TGFB2-related_disorder|Loeys-Dietz_syndrome_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_4|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Loeys-Dietz_syndrome_4": 1,
    "Hypermanganesemia_with_dystonia|_polycythemia|_and_cirrhosis": 43,
    "Hypermanganesemia_with_dystonia|_polycythemia|_and_cirrhosis|not_provided": 14,
    "not_provided|Hypermanganesemia_with_dystonia|_polycythemia|_and_cirrhosis": 2,
    "not_provided|Hypermanganesemia_with_dystonia|_polycythemia|_and_cirrhosis|Inborn_genetic_diseases": 1,
    "SLC30A10-related_disorder": 1,
    "SLC30A10-related_disorder|not_provided": 2,
    "Congenital_Erythrocytosis": 1,
    "SLC30A10-related_disorder|not_provided|Hypermanganesemia_with_dystonia|_polycythemia|_and_cirrhosis": 2,
    "not_specified|not_provided|Hypermanganesemia_with_dystonia|_polycythemia|_and_cirrhosis": 1,
    "Leukodystrophy|_hypomyelinating|_15": 18,
    "EPRS1-related_disorder|not_provided": 13,
    "Leukodystrophy|_hypomyelinating|_15|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Leukodystrophy|_hypomyelinating|_15": 2,
    "not_provided|EPRS1-related_disorder": 8,
    "Inborn_genetic_diseases|EPRS1-related_disorder": 1,
    "not_provided|Leukodystrophy|_hypomyelinating|_15": 6,
    "not_provided|Inborn_genetic_diseases|EPRS1-related_disorder|Leukodystrophy|_hypomyelinating|_15": 1,
    "Leukodystrophy|_hypomyelinating|_15|Inborn_genetic_diseases|not_provided": 1,
    "Leukodystrophy|_hypomyelinating|_15|not_provided|Inborn_genetic_diseases": 1,
    "EPRS1-related_disorder": 4,
    "EPRS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|EPRS1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Leukodystrophy|_hypomyelinating|_15|Inborn_genetic_diseases": 1,
    "Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome": 12,
    "Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome|not_provided": 4,
    "not_provided|IARS2-related_disorder|not_specified": 2,
    "not_specified|IARS2-related_disorder|not_provided": 1,
    "not_provided|IARS2-related_disorder": 1,
    "IARS2-related_disorder|not_specified|not_provided": 1,
    "IARS2-related_disorder|not_provided": 5,
    "not_provided|Leigh_syndrome": 69,
    "IARS2-related_disorder": 2,
    "not_provided|not_specified|IARS2-related_disorder": 1,
    "not_provided|Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome": 2,
    "Leigh_syndrome|not_provided|Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome": 1,
    "Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome|not_specified|not_provided|Leigh_syndrome": 1,
    "Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "Leigh_syndrome|not_provided": 64,
    "Cataract-growth_hormone_deficiency-sensory_neuropathy-sensorineural_hearing_loss-skeletal_dysplasia_syndrome|not_provided|growth_hormone_deficiency_with_short_stature|partial_sensorineural_deafness|Cataract|Peripheral_neuropathy": 1,
    "Warburg_micro_syndrome|Martsolf_syndrome": 8,
    "Martsolf_syndrome|Warburg_micro_syndrome": 8,
    "Warburg_micro_syndrome_2|Martsolf_syndrome": 224,
    "Martsolf_syndrome|Warburg_micro_syndrome_2": 155,
    "Warburg_micro_syndrome_2|not_provided|Martsolf_syndrome": 2,
    "Martsolf_syndrome|not_provided|Warburg_micro_syndrome_2": 1,
    "not_provided|Warburg_micro_syndrome_2|Martsolf_syndrome": 13,
    "not_provided|Warburg_micro_syndrome|Martsolf_syndrome": 1,
    "not_provided|Martsolf_syndrome|Warburg_micro_syndrome_2": 10,
    "RAB3GAP2-related_disorder|Martsolf_syndrome|Warburg_micro_syndrome_2|not_specified|not_provided": 1,
    "RAB3GAP2-related_disorder|Warburg_micro_syndrome_2|Martsolf_syndrome|not_specified|not_provided": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Warburg_micro_syndrome_2|Martsolf_syndrome": 2,
    "RAB3GAP2-related_disorder|Warburg_micro_syndrome_2|Martsolf_syndrome": 3,
    "Inborn_genetic_diseases|Warburg_micro_syndrome_2|Martsolf_syndrome": 8,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|RAB3GAP2-related_disorder|not_provided|not_specified": 2,
    "Warburg_micro_syndrome_2|Martsolf_syndrome_1": 2,
    "RAB3GAP2-related_disorder|Martsolf_syndrome|Warburg_micro_syndrome_2|not_specified": 1,
    "RAB3GAP2-related_disorder|Martsolf_syndrome|Warburg_micro_syndrome_2|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Warburg_micro_syndrome_2|Martsolf_syndrome": 1,
    "Inborn_genetic_diseases|Martsolf_syndrome|Warburg_micro_syndrome_2": 4,
    "Martsolf_syndrome_1": 27,
    "Warburg_micro_syndrome_2|See_cases": 1,
    "not_provided|Martsolf_syndrome|Warburg_micro_syndrome_2|Amenorrhea": 1,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|RAB3GAP2-related_disorder": 3,
    "not_specified|Warburg_micro_syndrome_2|Martsolf_syndrome": 4,
    "Martsolf_syndrome|not_specified|not_provided|Warburg_micro_syndrome_2": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|RAB3GAP2-related_disorder|not_specified|Warburg_micro_syndrome_2|Martsolf_syndrome": 1,
    "Martsolf_syndrome": 4,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Warburg_micro_syndrome_2|Martsolf_syndrome": 2,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|Inborn_genetic_diseases": 5,
    "not_specified|Warburg_micro_syndrome_2|not_provided|Martsolf_syndrome": 1,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Warburg_micro_syndrome_2|Martsolf_syndrome_1|Martsolf_syndrome|not_provided": 1,
    "Martsolf_syndrome_1|Martsolf_syndrome": 1,
    "Warburg_micro_syndrome_2|not_provided|Martsolf_syndrome|RAB3GAP2-related_disorder|Martsolf_syndrome_1": 1,
    "not_provided|Martsolf_syndrome|Warburg_micro_syndrome_2|Inborn_genetic_diseases": 1,
    "Warburg_micro_syndrome_2": 11,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|RAB3GAP2-related_disorder": 1,
    "Martsolf_syndrome|not_provided|Warburg_micro_syndrome_2|not_specified": 1,
    "not_specified|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "RAB3GAP2-related_disorder": 5,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|not_provided|not_specified": 1,
    "Warburg_micro_syndrome_2|not_specified|Martsolf_syndrome|not_provided": 2,
    "Martsolf_syndrome|Warburg_micro_syndrome|Warburg_micro_syndrome_2": 1,
    "Martsolf_syndrome|not_specified|RAB3GAP2-related_disorder|Warburg_micro_syndrome_2": 1,
    "not_provided|RAB3GAP2-related_disorder|Warburg_micro_syndrome_2|Martsolf_syndrome": 1,
    "Inborn_genetic_diseases|Warburg_micro_syndrome_2|Martsolf_syndrome_1": 1,
    "Martsolf_syndrome|Inborn_genetic_diseases|Warburg_micro_syndrome_2": 2,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|not_specified|not_provided": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|RAB3GAP2-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Warburg_micro_syndrome_2": 1,
    "not_provided|not_specified|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|Martsolf_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|not_provided|not_specified": 1,
    "Warburg_micro_syndrome|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|Inborn_genetic_diseases|Martsolf_syndrome_1": 1,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|Martsolf_syndrome|RAB3GAP2-related_disorder|Warburg_micro_syndrome_2": 1,
    "Inborn_genetic_diseases|Martsolf_syndrome_1|Warburg_micro_syndrome_2|not_provided|RAB3GAP2-related_disorder|Martsolf_syndrome|Amenorrhea": 1,
    "Martsolf_syndrome|not_specified|Warburg_micro_syndrome_2|not_provided": 1,
    "not_specified|RAB3GAP2-related_disorder|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "Martsolf_syndrome_1|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|Amenorrhea|not_provided|Martsolf_syndrome_1": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|RAB3GAP2-related_disorder|not_specified": 1,
    "Martsolf_syndrome|Martsolf_syndrome_1|Warburg_micro_syndrome_2|not_specified": 1,
    "Developmental_cataract|Microcephaly|Microphthalmia|Persistent_pupillary_membrane|Warburg_micro_syndrome_2": 1,
    "not_provided|Warburg_micro_syndrome_2|Martsolf_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|RAB3GAP2-related_disorder|not_provided|Warburg_micro_syndrome_2|Martsolf_syndrome": 1,
    "not_provided|Warburg_micro_syndrome|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "Warburg_micro_syndrome_2|not_provided|not_specified|Martsolf_syndrome": 1,
    "not_provided|Martsolf_syndrome|Warburg_micro_syndrome|Warburg_micro_syndrome_2": 1,
    "Martsolf_syndrome|not_provided|Warburg_micro_syndrome|Warburg_micro_syndrome_2": 1,
    "Inborn_genetic_diseases|Martsolf_syndrome_1|not_provided": 1,
    "Microcephaly|Martsolf_syndrome|Warburg_micro_syndrome_2": 1,
    "Warburg_micro_syndrome_2|Martsolf_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|Martsolf_syndrome|Warburg_micro_syndrome_2|not_provided": 1,
    "Martsolf_syndrome|Warburg_micro_syndrome_2|not_specified": 1,
    "Inborn_genetic_diseases|Warburg_micro_syndrome_2|Martsolf_syndrome|not_provided": 1,
    "not_provided|Warburg_micro_syndrome_2|Martsolf_syndrome|RAB3GAP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Martsolf_syndrome|not_provided|RAB3GAP2-related_disorder|Warburg_micro_syndrome_2": 1,
    "Warburg_micro_syndrome|not_provided|Martsolf_syndrome": 1,
    "HLX-related_disorder": 3,
    "not_specified|HLX-related_disorder": 1,
    "Cardiomyopathy|_familial_restrictive|_6|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_6": 4,
    "Odontochondrodysplasia2_with_hearing_loss_and_diabetes": 1,
    "ODONTOCHONDRODYSPLASIA_WITH_HEARING_LOSS_AND_DIABETES": 1,
    "Odontochondrodysplasia_2_with_hearing_loss_and_diabetes": 4,
    "MIA3-related_condition": 1,
    "DISP1-related_disorder|not_provided": 7,
    "DISP1-related_disorder": 13,
    "not_provided|DISP1-related_disorder": 10,
    "not_provided|Microform_holoprosencephaly": 1,
    "Microform_holoprosencephaly": 7,
    "Holoprosencephaly_sequence|not_provided": 21,
    "Holoprosencephaly_7": 10,
    "DISP1-related_Holoprosencephaly|DISP1-related_disorder": 1,
    "Lobar_holoprosencephaly": 2,
    "Holoprosencephaly_sequence": 174,
    "Holoprosencephaly_10": 2,
    "Microform_holoprosencephaly|not_provided": 2,
    "not_provided|not_specified|DISP1-related_disorder": 1,
    "not_specified|not_provided|DISP1-related_disorder": 1,
    "not_specified|DISP1-related_disorder|not_provided": 1,
    "Esophageal_atresia|Holoprosencephaly_10|not_specified": 1,
    "TLR5-related_disorder": 4,
    "Legionnaire_disease|_susceptibility_to|TLR5-related_disorder": 1,
    "Systemic_lupus_erythematosus|_resistance_to|_1|Legionnaire_disease|_susceptibility_to|Melioidosis|_resistance_to": 1,
    "Systemic_lupus_erythematosus|_susceptibility_to|_1": 1,
    "TP53BP2-related_disorder": 14,
    "not_provided|TP53BP2-related_disorder": 6,
    "TP53BP2-related_disorder|not_provided": 2,
    "FBXO28-related_disorder": 7,
    "Developmental_and_epileptic_encephalopathy_100": 9,
    "FBXO28-related_developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_100": 1,
    "FBXO28-associated_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|See_cases|Developmental_and_epileptic_encephalopathy_100|not_provided": 1,
    "Leukodystrophy|_hypomyelinating|_18": 12,
    "DEGS1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|DEGS1-related_disorder": 2,
    "Leukodystrophy|_hypomyelinating|_18|Inborn_genetic_diseases": 3,
    "DEGS1-related_Hypomyelinating_Leukodystrophy": 1,
    "DEGS1-related_Hypomyelinating_Leukodystrophy|Leukodystrophy|_hypomyelinating|_18": 1,
    "not_provided|Leukodystrophy|_hypomyelinating|_18": 2,
    "DEGS1-related_disorder|not_provided": 2,
    "Leukodystrophy|_hypomyelinating|_18|not_provided|Leukodystrophy": 1,
    "DEGS1-related_disorder": 1,
    "WDR26-related_disorder": 12,
    "not_provided|Skraban-Deardorff_syndrome": 4,
    "Skraban-Deardorff_syndrome": 51,
    "Inborn_genetic_diseases|Skraban-Deardorff_syndrome": 2,
    "Skraban-Deardorff_syndrome|not_provided": 4,
    "Skraban-Deardorff_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|WDR26-related_disorder|not_specified": 1,
    "Neurofibromatosis|_type_1|Inborn_genetic_diseases": 3,
    "Intellectual_disability|_seizures|_abnormal_gait_and_distinctive_facial_features": 1,
    "WDR26-related_disorder|Skraban-Deardorff_syndrome|not_provided": 1,
    "DNAH14-related_disorder": 8,
    "DNAH14-related_disorder|not_provided": 2,
    "not_provided|DNAH14-related_disorder": 6,
    "Hypotonia|Intellectual_disability|_severe|Delayed_speech_and_language_development|Seizure|Microcephaly": 2,
    "DNAH14-related_neurodevelopmental_disorder": 4,
    "not_provided|DNAH14-related_neurodevelopmental_disorder": 1,
    "not_specified|DNAH14-Associated_Neurodevelopmental_Disorder": 1,
    "DNAH14-Associated_Neurodevelopmental_Disorder": 1,
    "Greenberg_dysplasia": 39,
    "Greenberg_dysplasia|not_provided": 6,
    "not_provided|Greenberg_dysplasia": 18,
    "not_provided|Greenberg_dysplasia|Inborn_genetic_diseases": 2,
    "LBR-related_disorder|not_provided": 2,
    "not_provided|LBR-related_disorder": 3,
    "not_provided|Greenberg_dysplasia|Reynolds_syndrome|Regressive_spondylometaphyseal_dysplasia|Pelger-Hu\u00ebt_anomaly": 3,
    "RHIZOMELIC_SKELETAL_DYSPLASIA_WITH_PELGER-HUET_ANOMALY|not_provided": 2,
    "Pelger-Hu\u00ebt_anomaly|Short_long_bone|Rhizomelic_leg_shortening|Retrognathia|Femoral_bowing|Disproportionate_short_stature|Rhizomelic_arm_shortening": 1,
    "Pelger-Hu\u00ebt_anomaly": 5,
    "not_provided|LBR-related_disorder|RHIZOMELIC_SKELETAL_DYSPLASIA_WITH_PELGER-HUET_ANOMALY|Anadysplasia-like|_spontaneously_remitting_spondylometaphyseal_dysplasia|Reynolds_syndrome|Greenberg_dysplasia": 1,
    "Greenberg_dysplasia|Pelger-Hu\u00ebt_anomaly": 3,
    "Connective_tissue_disorder|not_provided|Greenberg_dysplasia": 1,
    "Regressive_spondylometaphyseal_dysplasia|Greenberg_dysplasia|not_provided": 1,
    "RHIZOMELIC_SKELETAL_DYSPLASIA_WITH_PELGER-HUET_ANOMALY|Pelger-Hu\u00ebt_anomaly": 1,
    "not_provided|Connective_tissue_disorder|Greenberg_dysplasia": 1,
    "Greenberg_dysplasia|LBR-related_disorder|Jeune_thoracic_dystrophy|Regressive_spondylometaphyseal_dysplasia|not_provided": 1,
    "Greenberg_dysplasia|not_provided|LBR-related_disorder": 3,
    "Inborn_genetic_diseases|LBR-related_disorder": 1,
    "Reynolds_syndrome|Greenberg_dysplasia|Regressive_spondylometaphyseal_dysplasia|Pelger-Hu\u00ebt_anomaly": 1,
    "LBR-related_disorder": 3,
    "RHIZOMELIC_SKELETAL_DYSPLASIA_WITHOUT_PELGER-HUET_ANOMALY|Connective_tissue_disorder|not_provided|Pelger-Hu\u00ebt_anomaly|Reynolds_syndrome|Regressive_spondylometaphyseal_dysplasia|Greenberg_dysplasia": 1,
    "not_provided|Inborn_genetic_diseases|Greenberg_dysplasia": 2,
    "Connective_tissue_disorder|Greenberg_dysplasia|not_provided": 3,
    "not_provided|Greenberg_dysplasia|Connective_tissue_disorder": 2,
    "not_provided|Regressive_spondylometaphyseal_dysplasia|Reynolds_syndrome|Pelger-Hu\u00ebt_anomaly|Greenberg_dysplasia": 1,
    "LBR-related_disorder|not_provided|Greenberg_dysplasia": 2,
    "Jeune_thoracic_dystrophy|not_provided": 43,
    "Inborn_genetic_diseases|Greenberg_dysplasia": 1,
    "Inborn_genetic_diseases|Greenberg_dysplasia|not_provided": 1,
    "Greenberg_dysplasia|Regressive_spondylometaphyseal_dysplasia|Reynolds_syndrome|not_provided": 1,
    "Greenberg_dysplasia|Regressive_spondylometaphyseal_dysplasia|not_provided": 1,
    "not_provided|Connective_tissue_disorder|Greenberg_dysplasia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Greenberg_dysplasia": 1,
    "Connective_tissue_disorder|LBR-related_disorder|not_provided": 1,
    "not_specified|LBR-related_disorder|not_provided|Inborn_genetic_diseases|Connective_tissue_disorder|Greenberg_dysplasia": 1,
    "Regressive_spondylometaphyseal_dysplasia": 1,
    "Greenberg_dysplasia|LBR-related_disorder|not_provided|not_specified": 1,
    "Regressive_spondylometaphyseal_dysplasia|Pelger-Hu\u00ebt_anomaly|Reynolds_syndrome|Greenberg_dysplasia|not_provided": 1,
    "Greenberg_dysplasia|Connective_tissue_disorder|Reynolds_syndrome|Regressive_spondylometaphyseal_dysplasia|Pelger-Hu\u00ebt_anomaly|not_provided|not_specified": 1,
    "Greenberg_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "RHIZOMELIC_SKELETAL_DYSPLASIA_WITH_PELGER-HUET_ANOMALY": 1,
    "Greenberg_dysplasia|Inborn_genetic_diseases": 1,
    "not_specified|Reynolds_syndrome|Pelger-Hu\u00ebt_anomaly|Greenberg_dysplasia|not_provided": 1,
    "not_provided|Pelger-Hu\u00ebt_anomaly": 1,
    "not_provided|Greenberg_dysplasia|LBR-related_disorder": 1,
    "Greenberg_dysplasia|not_provided|Inborn_genetic_diseases|Regressive_spondylometaphyseal_dysplasia|Pelger-Hu\u00ebt_anomaly|Reynolds_syndrome": 1,
    "not_provided|Greenberg_dysplasia|Pelger-Hu\u00ebt_anomaly|Regressive_spondylometaphyseal_dysplasia": 1,
    "not_provided|Greenberg_dysplasia|Reynolds_syndrome|Pelger-Hu\u00ebt_anomaly|not_specified": 1,
    "RHIZOMELIC_SKELETAL_DYSPLASIA_WITH_PELGER-HUET_ANOMALY|Anadysplasia-like|_spontaneously_remitting_spondylometaphyseal_dysplasia|Greenberg_dysplasia": 1,
    "not_specified|not_provided|Reynolds_syndrome|Pelger-Hu\u00ebt_anomaly|Greenberg_dysplasia": 1,
    "LBR-related_disorder|Greenberg_dysplasia|not_provided": 1,
    "EPHX1-related_disorder": 3,
    "Hereditary_lipodystrophy": 1,
    "Cystic_fibrosis|EPOXIDE_HYDROLASE_1_POLYMORPHISM|not_provided": 1,
    "not_provided|EPOXIDE_HYDROLASE_1_POLYMORPHISM": 1,
    "not_provided|EPHX1-related_disorder": 1,
    "Hypercholanemia|_familial_1": 58,
    "Leukodystrophy|_hypomyelinating|_19|_transient_infantile": 20,
    "Inborn_genetic_diseases|Leukodystrophy|_hypomyelinating|_19|_transient_infantile": 1,
    "TMEM63A-related_disorder|not_provided": 2,
    "TMEM63A-related_disorder": 3,
    "not_provided|TMEM63A-related_disorder": 1,
    "Leukodystrophy|_hypomyelinating|_19|_transient_infantile|Leukodystrophy": 3,
    "Leukodystrophy|_hypomyelinating|_19|_transient_infantile|not_provided": 1,
    "TMEM63A-related_disorder|not_provided|not_specified": 1,
    "TMEM63A-related_disorder|Leukodystrophy|_hypomyelinating|_19|_transient_infantile|not_provided": 1,
    "TMEM63A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "TMEM63A-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TMEM63A-related_disorder": 1,
    "not_specified|Hypomyelinating_leukodystrophy_10|not_provided": 1,
    "Hypomyelinating_leukodystrophy_10|not_provided": 9,
    "Leukodystrophy|Hypomyelinating_leukodystrophy_10|not_provided": 1,
    "Hypomyelinating_leukodystrophy_10": 21,
    "not_provided|Hypomyelinating_leukodystrophy_10": 6,
    "PYCR2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hypomyelinating_leukodystrophy_10|not_specified": 1,
    "Left-right_axis_malformations": 96,
    "not_provided|Left-right_axis_malformations": 3,
    "not_specified|Left-right_axis_malformations": 11,
    "LEFTY2-related_disorder|Left-right_axis_malformations|not_specified": 1,
    "Left-right_axis_malformations|not_specified": 12,
    "Left-right_axis_malformations|not_specified|LEFTY2-related_disorder": 1,
    "not_provided|Left-right_axis_malformations|not_specified": 3,
    "Left-right_axis_malformations|not_provided": 2,
    "Left-right_axis_malformations|not_specified|not_provided": 3,
    "Left-right_axis_malformations|LEFTY2-related_disorder": 3,
    "See_cases|Left-right_axis_malformations": 1,
    "LEFTY2-related_disorder": 2,
    "LEFTY2-related_disorder|Left-right_axis_malformations": 2,
    "Left-right_axis_malformations|not_provided|not_specified": 1,
    "LEFTY2-related_disorder|not_specified": 1,
    "Visceral_heterotaxy": 23,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|not_provided": 1,
    "not_provided|H3-3A-related_disorder": 1,
    "H3-3A-related_disorder|not_provided": 1,
    "Glioblastoma": 4,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|Brain_imaging_abnormality|Delayed_speech_and_language_development|Intellectual_disability|Global_developmental_delay|Short_stature": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1": 5,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|Inborn_genetic_diseases": 2,
    "Intellectual_disability|Global_developmental_delay|Brain_imaging_abnormality|Delayed_speech_and_language_development|Short_stature": 3,
    "H3-3A-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder|Bryant-Li-Bhoj_neurodevelopmental_syndrome_1": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|Intellectual_disability|Global_developmental_delay|Brain_imaging_abnormality|Delayed_speech_and_language_development|Short_stature": 2,
    "H3-3A-related_disorder": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|not_specified": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|not_provided|Global_developmental_delay|Intellectual_disability|Delayed_speech_and_language_development|Brain_imaging_abnormality|Short_stature": 1,
    "H3F3A-related_disorder|Inborn_genetic_diseases": 1,
    "Delayed_speech_and_language_development|Short_stature|Intellectual_disability|Global_developmental_delay|Brain_imaging_abnormality|not_provided|not_specified|Bryant-Li-Bhoj_neurodevelopmental_syndrome_1": 1,
    "H3F3A-related_disorder|not_provided|Bryant-Li-Bhoj_neurodevelopmental_syndrome_1|Inborn_genetic_diseases": 1,
    "PARP1-related_disorder": 10,
    "not_provided|PARP1-related_disorder": 6,
    "Hereditary_renal_cell_carcinoma": 1,
    "ITPKB-related_disorder": 2,
    "ITPKB-related_disorder|not_specified|Myeloproliferative_neoplasm|_unclassifiable": 2,
    "not_specified|ITPKB-related_disorder": 2,
    "not_specified|Myeloproliferative_neoplasm|_unclassifiable": 4,
    "Dilated_Cardiomyopathy|_Dominant|Early-onset_autosomal_dominant_Alzheimer_disease": 7,
    "Alzheimer_disease_4|not_provided|Dilated_cardiomyopathy_1V": 1,
    "Alzheimer_disease_4|Dilated_cardiomyopathy_1V": 19,
    "Dilated_cardiomyopathy_1V|Alzheimer_disease_4": 16,
    "Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_provided": 7,
    "PSEN2-related_disorder": 7,
    "Alzheimer_disease_4": 103,
    "Inborn_genetic_diseases|Alzheimer_disease_4|Dilated_cardiomyopathy_1V": 2,
    "Vascular_dementia|Alzheimer_disease_4|not_specified": 1,
    "not_specified|Alzheimer_disease_4|PSEN2-related_disorder": 1,
    "Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_provided|not_specified": 4,
    "Alzheimer_disease_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_provided": 1,
    "not_provided|Alzheimer_disease_4|Dilated_cardiomyopathy_1V": 7,
    "Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Alzheimer_disease_4": 12,
    "not_specified|PSEN2-related_disorder|not_provided|Alzheimer_disease_4": 1,
    "not_specified|Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_provided|PSEN2-related_disorder": 1,
    "not_specified|not_provided|Alzheimer_disease_4|Dilated_cardiomyopathy_1V|Alzheimer_disease": 1,
    "Alzheimer_disease_4|not_specified": 2,
    "Dilated_cardiomyopathy_1V|Alzheimer_disease_4|not_provided": 2,
    "Alzheimer_disease_4|not_specified|not_provided": 1,
    "PSEN2-related_disorder|Alzheimer_disease_4|not_provided": 1,
    "not_provided|not_specified|Alzheimer_disease_4|Dilated_cardiomyopathy_1V": 1,
    "not_specified|Dilated_cardiomyopathy_1V": 1,
    "Alzheimer_disease_4|not_provided": 4,
    "PSEN2-related_disorder|Alzheimer_disease_4": 3,
    "Alzheimer_disease_4|PSEN2-related_disorder": 5,
    "not_provided|Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_specified": 1,
    "PSEN2-related_disorder|Alzheimer_disease|not_provided|not_specified|Dilated_cardiomyopathy_1V|Alzheimer_disease_4": 1,
    "Dilated_cardiomyopathy_1V|Alzheimer_disease_4|PSEN2-related_disorder|not_provided": 1,
    "not_specified|Alzheimer_disease_4": 2,
    "Inborn_genetic_diseases|Alzheimer_disease_4": 1,
    "Dilated_cardiomyopathy_1V|Alzheimer_disease_4|not_provided|not_specified": 1,
    "Huntington_disease-like_syndrome|not_provided|Alzheimer_disease_4": 1,
    "not_specified|not_provided|Alzheimer_disease_4|Dilated_cardiomyopathy_1V": 2,
    "Dilated_cardiomyopathy_1V": 1,
    "Inborn_genetic_diseases|Dilated_cardiomyopathy_1V|Alzheimer_disease_4": 1,
    "not_provided|not_specified|Alzheimer_disease_4": 1,
    "not_provided|Dilated_cardiomyopathy_1V|Alzheimer_disease_4|not_specified": 1,
    "Dilated_cardiomyopathy_1V|Alzheimer_disease_4|not_specified": 1,
    "PSEN2-related_disorder|not_provided|Alzheimer_disease_4": 1,
    "Alzheimer_disease_4|not_provided|Dilated_cardiomyopathy_1V|not_specified": 1,
    "Dilated_cardiomyopathy_1V|Alzheimer_disease_4|not_specified|not_provided": 1,
    "Alzheimer_disease_4|not_specified|Dilated_cardiomyopathy_1V": 1,
    "PSEN2-related_disorder|Inborn_genetic_diseases|not_provided|Alzheimer_disease_4": 1,
    "Alzheimer_disease_4|PSEN2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1V|Alzheimer_disease_4": 1,
    "Alzheimer_disease|not_provided|Alzheimer_disease_4": 1,
    "Alzheimer_disease_4|Dilated_cardiomyopathy_1V|not_specified": 1,
    "Autosomal_recessive_cerebellar_ataxia|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 3,
    "Autosomal_recessive_cerebellar_ataxia|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 5,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 6,
    "Autosomal_recessive_cerebellar_ataxia|not_specified|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 41,
    "not_provided|not_specified|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided": 26,
    "not_provided|Autosomal_recessive_cerebellar_ataxia|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_specified": 1,
    "not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 32,
    "Autosomal_recessive_cerebellar_ataxia|not_specified|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 2,
    "not_specified|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|Autosomal_recessive_cerebellar_ataxia": 1,
    "Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|not_specified|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Coenzyme_Q10_deficiency|_primary|_1": 25,
    "not_provided|COQ8A-related_disorder": 8,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|COQ8A-related_disorder|not_provided": 1,
    "COQ8A-related_disorder|not_specified|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 2,
    "not_provided|Autosomal_recessive_cerebellar_ataxia|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 2,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|COQ8A-related_disorder|not_specified|not_provided": 1,
    "not_provided|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 4,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|COQ8A-related_disorder|not_specified": 1,
    "COQ8A-related_disorder|not_provided|not_specified": 1,
    "COQ8A-related_disorder": 5,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_specified|not_provided": 4,
    "COQ8A-related_disorder|not_provided": 2,
    "Autosomal_recessive_cerebellar_ataxia|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|Autosomal_recessive_cerebellar_ataxia|not_provided": 1,
    "not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|not_specified|COQ8A-related_disorder": 2,
    "Mitochondrial_disease": 119,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|See_cases": 1,
    "Cerebellar_ataxia": 15,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|not_specified": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|COQ8A-related_disorder": 4,
    "COQ8A-related_disorder|not_specified|not_provided": 2,
    "Coenzyme_Q10_deficiency|not_specified|not_provided|Joubert_syndrome_17|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Mitochondrial_disease|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_specified": 2,
    "not_specified|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 2,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Autosomal_recessive_cerebellar_ataxia": 3,
    "not_provided|not_specified|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Autosomal_recessive_cerebellar_ataxia": 1,
    "Global_developmental_delay|not_provided": 5,
    "Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 2,
    "not_specified|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_specified|COQ8A-related_disorder|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_cerebellar_ataxia|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "not_specified|not_provided|COQ8A-related_disorder|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "not_specified|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided": 1,
    "COQ8A-related_disorder|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "not_specified|Autosomal_recessive_cerebellar_ataxia|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 3,
    "not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Abnormality_of_the_nervous_system|See_cases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 2,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Autosomal_recessive_cerebellar_ataxia|not_provided": 1,
    "COQ8A-related_disorder|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "not_specified|Autosomal_recessive_cerebellar_ataxia|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Cerebellar_ataxia|Slightly_reduced_reflexes|Dysdiadochokinesis|Dysmetria|Slurred_speech|Cerebellar_atrophy|Nystagmus": 1,
    "COQ8A-related_disorder|not_provided|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "COQ8A-related_disorder|not_specified|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|not_specified|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|COQ8A-related_disorder": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_specified|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|not_provided": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided|Autosomal_recessive_cerebellar_ataxia": 2,
    "not_provided|Autosomal_recessive_cerebellar_ataxia|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type": 1,
    "Autosomal_recessive_cerebellar_ataxia|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|not_provided": 1,
    "Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency": 1,
    "Autosomal_recessive_ataxia_due_to_ubiquinone_deficiency|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|Autosomal_recessive_cerebellar_ataxia|not_provided": 1,
    "Autosomal_recessive_cerebellar_ataxia|Coenzyme_Q10_deficiency|_Spinocerebellar_Ataxia_Type|not_provided": 1,
    "WNT3A-related_disorder|not_provided": 1,
    "Periventricular_nodular_heterotopia_8": 14,
    "ARF1-related_disorder": 5,
    "Inborn_genetic_diseases|Periventricular_nodular_heterotopia_8": 1,
    "Periventricular_nodular_heterotopia_8|not_provided": 1,
    "not_provided|Periventricular_nodular_heterotopia_8": 1,
    "ARF1-related_disorder|not_provided": 1,
    "Mitochondrial_dna_depletion_syndrome_21": 4,
    "Spastic_paraplegia|Hypomyelinating_leukodystrophy_2": 2,
    "Spastic_paraplegia|not_provided|Hypomyelinating_leukodystrophy_2": 1,
    "Hypomyelinating_leukodystrophy_2": 42,
    "Lymphatic_malformation_3|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_44|Hypomyelinating_leukodystrophy_2": 1,
    "Hypomyelinating_leukodystrophy_2|not_provided": 3,
    "Inborn_genetic_diseases|Spastic_paraplegia": 250,
    "Lymphatic_malformation_3": 6,
    "Spastic_paraplegia|GJC2-related_disorder": 1,
    "Spastic_paraplegia|not_specified|not_provided": 16,
    "Intellectual_disability|Dystonic_disorder|Hypomyelinating_leukodystrophy_2|Lymphatic_malformation_3": 1,
    "Hereditary_spastic_paraplegia_44": 2,
    "Hereditary_spastic_paraplegia|Hypomyelinating_leukodystrophy_2|Hereditary_spastic_paraplegia_44|Lymphatic_malformation_3|Spastic_paraplegia|not_specified|not_provided": 1,
    "Hypomyelinating_leukodystrophy_2|Spastic_paraplegia": 3,
    "not_provided|Spastic_paraplegia|Inborn_genetic_diseases": 21,
    "not_specified|Spastic_paraplegia": 75,
    "Lymphatic_malformation_3|not_provided": 3,
    "GJC2-related_disorder|Spastic_paraplegia": 2,
    "Hypomyelinating_leukodystrophy_2|Hereditary_spastic_paraplegia_44": 2,
    "not_specified|Hypomyelinating_leukodystrophy_2": 1,
    "not_provided|Spastic_paraplegia|Hypomyelinating_leukodystrophy_2|not_specified": 1,
    "Hypomyelinating_leukodystrophy_2|Lymphatic_malformation_3|Hereditary_spastic_paraplegia_44": 1,
    "Hereditary_spastic_paraplegia|GJC2-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hypomyelinating_leukodystrophy_2|Spastic_ataxia|not_provided": 1,
    "GJC2-related_disorder": 2,
    "Inborn_genetic_diseases|Lymphatic_malformation_3|Hereditary_spastic_paraplegia_44|Hypomyelinating_leukodystrophy_2|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|Hypomyelinating_leukodystrophy_2|Lymphatic_malformation_3|Hereditary_spastic_paraplegia_44": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia": 35,
    "Spastic_paraplegia|not_provided|GJC2-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Hypomyelinating_leukodystrophy_2": 4,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|GJC2-related_disorder": 1,
    "Spastic_paraplegia|Pelizaeus-Merzbacher_disease": 1,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided": 1,
    "GJC2-related_disorder|not_provided": 1,
    "Hypomyelinating_leukodystrophy_2|not_provided|Spastic_paraplegia": 1,
    "Abnormality_of_the_nervous_system|Hypomyelinating_leukodystrophy_2": 1,
    "Hypomyelinating_leukodystrophy_2|See_cases": 1,
    "not_specified|Spastic_paraplegia|Lymphatic_malformation_3": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|not_provided": 3,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|not_specified": 1,
    "Abnormality_of_the_nervous_system|Hypomyelinating_leukodystrophy_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spastic_paraplegia": 13,
    "Spastic_paraplegia|GJC2-related_disorder|Hereditary_spastic_paraplegia_44|Lymphatic_malformation_3|Hypomyelinating_leukodystrophy_2": 1,
    "Hereditary_spastic_paraplegia_44|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_44|Lymphatic_malformation_3|Hypomyelinating_leukodystrophy_2": 1,
    "GJC2-related_disorder|Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Lymphatic_malformation_3|not_provided": 1,
    "Spastic_paraplegia|not_provided|Inborn_genetic_diseases": 11,
    "not_specified|Hypomyelinating_leukodystrophy_2|Lymphatic_malformation_3|Hereditary_spastic_paraplegia_44|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_44|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_provided": 27,
    "not_provided|Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|Inborn_genetic_diseases": 4,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|not_provided|Inborn_genetic_diseases": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_3": 13,
    "Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3": 70,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74": 3,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74": 65,
    "IBA57-related_disorder": 4,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74": 4,
    "Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|Inborn_genetic_diseases": 4,
    "Hereditary_spastic_paraplegia_74|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_3|not_specified": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|not_provided": 10,
    "not_specified|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|IBA57-related_disorder": 1,
    "Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|not_specified": 2,
    "not_provided|Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3": 3,
    "Hereditary_spastic_paraplegia_74": 2,
    "not_provided|not_specified|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3": 3,
    "not_specified|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74": 2,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_3": 2,
    "Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|not_provided": 3,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|Inborn_genetic_diseases|IBA57-related_disorder|not_provided": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|IBA57-related_disorder": 3,
    "IBA57-related_disorder|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74": 1,
    "IBA57-related_disorder|not_provided|Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|not_provided": 3,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|IBA57-related_disorder|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|Inborn_genetic_diseases|not_provided": 2,
    "Multiple_mitochondrial_dysfunctions_syndrome_3|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_74": 1,
    "Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|not_specified|not_provided": 1,
    "IBA57-related_disorder|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3|not_provided": 1,
    "C1orf69/IBA57-related_disorder|Hereditary_spastic_paraplegia_74|Multiple_mitochondrial_dysfunctions_syndrome_3": 1,
    "Inborn_genetic_diseases|Multiple_mitochondrial_dysfunctions_syndrome_3|Hereditary_spastic_paraplegia_74|not_provided": 1,
    "not_provided|OBSCN-related_disorder": 57,
    "not_provided|not_specified|OBSCN-related_disorder": 14,
    "OBSCN-related_disorder|not_provided": 41,
    "OBSCN-related_disorder|not_specified": 41,
    "OBSCN-related_disorder|not_specified|not_provided": 35,
    "Rhabdomyolysis|_susceptibility_to|_1": 14,
    "not_specified|not_provided|OBSCN-related_disorder": 9,
    "not_specified|OBSCN-related_disorder": 16,
    "OBSCN-related_disorder": 66,
    "OBSCN-related_disorder|not_provided|not_specified": 14,
    "not_provided|OBSCN-related_disorder|not_specified": 11,
    "not_provided|OBSCN-related_disorder|Rhabdomyolysis|_susceptibility_to|_1": 1,
    "not_specified|OBSCN-related_disorder|not_provided": 6,
    "Rhabdomyolysis|_susceptibility_to|_1|not_provided": 2,
    "Rhabdomyolysis|_susceptibility_to|_1|not_specified": 1,
    "not_specified|Short_stature": 4,
    "not_specified|Rhabdomyolysis|_susceptibility_to|_1": 2,
    "Rhabdomyolysis|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Hypertrophic_cardiomyopathy_1": 1,
    "OBSCN-related_disorder|not_specified|Rhabdomyolysis|_susceptibility_to|_1|not_provided": 1,
    "OBSCN-related_disorder|Rhabdomyolysis|_susceptibility_to|_1|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_120": 4,
    "Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy|Familial_restrictive_cardiomyopathy": 5,
    "Actin_accumulation_myopathy": 301,
    "Congenital_myopathy_with_fiber_type_disproportion|Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy": 4,
    "Actin_accumulation_myopathy|Alpha-actinopathy": 1,
    "Alpha-actinopathy": 6,
    "Familial_restrictive_cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy": 1,
    "Nemaline_myopathy": 70,
    "Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Familial_restrictive_cardiomyopathy": 1,
    "Alpha-actinopathy|Actin_accumulation_myopathy|not_provided": 5,
    "not_specified|not_provided|Alpha-actinopathy": 1,
    "Alpha-actinopathy|Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant": 1,
    "Alpha-actinopathy|Actin_accumulation_myopathy": 5,
    "Actin_accumulation_myopathy|Alpha-actinopathy|not_provided": 5,
    "not_provided|Actin_accumulation_myopathy": 25,
    "ACTA1-related_myopathies": 1,
    "Progressive_scapulohumeroperoneal_distal_myopathy": 4,
    "ACTA1-related_disorder": 8,
    "Progressive_scapulohumeroperoneal_distal_myopathy|Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Alpha-actinopathy|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Actin_accumulation_myopathy|not_provided": 13,
    "Familial_restrictive_cardiomyopathy|not_specified|not_provided|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant": 6,
    "ACTA1-related_congenital_myopathy_disorders": 1,
    "Actin_accumulation_myopathy|Progressive_scapulohumeroperoneal_distal_myopathy|Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant": 1,
    "Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Actin_accumulation_myopathy|Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Primary_dilated_cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Alpha-actinopathy|Inborn_genetic_diseases|Actin_accumulation_myopathy": 1,
    "Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy|ACTA1-related_disorder|not_specified|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Actin_accumulation_myopathy|Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant": 3,
    "Nemaline_myopathy_2|Progressive_scapulohumeroperoneal_distal_myopathy|Actin_accumulation_myopathy|not_provided": 1,
    "Congenital_myopathy_4A|_autosomal_dominant|Progressive_scapulohumeroperoneal_distal_myopathy|Actin_accumulation_myopathy|not_provided": 1,
    "not_provided|ACTA1-related_myopathies|Nemaline_myopathy_3|_autosomal_dominant_or_recessive|Neurodevelopmental_delay": 1,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive": 3,
    "Familial_restrictive_cardiomyopathy|Nemaline_myopathy|Actin_accumulation_myopathy|not_specified|Alpha-actinopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy|Nemaline_myopathy": 3,
    "not_specified|Actin_accumulation_myopathy": 2,
    "Familial_restrictive_cardiomyopathy|not_specified|not_provided|Alpha-actinopathy|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Alpha-actinopathy|not_specified|not_provided": 1,
    "Actin_accumulation_myopathy|not_specified": 3,
    "Actin_accumulation_myopathy|Neuromuscular_disease": 2,
    "Familial_restrictive_cardiomyopathy|not_provided|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy|Progressive_scapulohumeroperoneal_distal_myopathy|ACTA1-related_myopathies|not_provided": 1,
    "Congenital_myopathy|Nemaline_myopathy": 1,
    "Primary_dilated_cardiomyopathy|Congenital_myopathy": 1,
    "Actin_accumulation_myopathy|Abnormality_of_the_musculature": 1,
    "ACTA1_gene_related_myopathy|Actin_accumulation_myopathy|not_provided": 1,
    "Actin_accumulation_myopathy|not_provided|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "ACTA1-related_disorder|Nemaline_myopathy": 1,
    "Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy": 1,
    "Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "not_specified|Alpha-actinopathy|Actin_accumulation_myopathy|not_provided": 1,
    "not_provided|Progressive_scapulohumeroperoneal_distal_myopathy|Actin_accumulation_myopathy": 1,
    "Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Actin_accumulation_myopathy|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy|ACTA1-related_disorder|Familial_restrictive_cardiomyopathy|not_provided": 1,
    "ACTA1-related_disorder|Actin_accumulation_myopathy": 2,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive|Alpha-actinopathy|ACTA1-related_disorder|not_provided|Actin_accumulation_myopathy": 1,
    "Nemaline_myopathy_3|_autosomal_dominant_or_recessive": 2,
    "not_provided|Alpha-actinopathy|Actin_accumulation_myopathy": 1,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive|Congenital_muscular_dystrophy_with_rigid_spine": 1,
    "Actin_accumulation_myopathy|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Progressive_scapulohumeroperoneal_distal_myopathy": 1,
    "Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy|not_provided": 1,
    "Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy": 1,
    "not_provided|not_specified|Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy|Familial_restrictive_cardiomyopathy|Progressive_scapulohumeroperoneal_distal_myopathy": 1,
    "Intranuclear_rod_myopathy": 1,
    "Alpha-actinopathy|Nemaline_myopathy|Centronuclear_myopathy": 1,
    "Actin_accumulation_myopathy|not_provided|Alpha-actinopathy": 1,
    "Alpha-actinopathy|not_provided|Actin_accumulation_myopathy": 3,
    "Fetal_akinesia_deformation_sequence|Fetal_akinesia": 1,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive|not_provided|Actin_accumulation_myopathy": 1,
    "Actin_accumulation_myopathy|not_provided|Alpha-actinopathy|Congenital_myopathy_with_fiber_type_disproportion|Progressive_scapulohumeroperoneal_distal_myopathy": 1,
    "Progressive_scapulohumeroperoneal_distal_myopathy|Actin_accumulation_myopathy|Congenital_myopathy_4A|_autosomal_dominant": 1,
    "Actin_accumulation_myopathy|ACTA1-related_myopathies": 1,
    "ACTA1-related_disorder|not_provided|Actin_accumulation_myopathy": 1,
    "Actin_accumulation_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive|Actin_accumulation_myopathy|ACTA1-related_myopathies": 1,
    "Alpha-actinopathy|Actin_accumulation_myopathy|Congenital_myopathy": 1,
    "Actin_accumulation_myopathy|not_specified|ACTA1-related_disorder": 1,
    "Alpha-actinopathy|Nemaline_myopathy|not_provided": 1,
    "Congenital_myopathy|Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Progressive_scapulohumeroperoneal_distal_myopathy|not_provided|Actin_accumulation_myopathy": 1,
    "Actin_accumulation_myopathy|not_specified|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "not_provided|Actin_accumulation_myopathy|Alpha-actinopathy": 1,
    "not_provided|not_specified|Familial_restrictive_cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|Actin_accumulation_myopathy": 2,
    "not_provided|Actin_accumulation_myopathy|not_specified": 1,
    "Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Actin_accumulation_myopathy|Alpha-actinopathy": 1,
    "Actin_accumulation_myopathy|ACTA1-related_disorder": 1,
    "Actin_accumulation_myopathy|not_provided|See_cases": 1,
    "Actin_accumulation_myopathy|Progressive_scapulohumeroperoneal_distal_myopathy": 1,
    "Congenital_myopathy_2b|_severe_infantile|_autosomal_recessive|Congenital_myopathy_2c|_severe_infantile|_autosomal_dominant|Actin_accumulation_myopathy|Progressive_scapulohumeroperoneal_distal_myopathy|not_provided": 1,
    "not_specified|Alpha-actinopathy|Actin_accumulation_myopathy": 1,
    "not_provided|Alpha-actinopathy|not_specified": 1,
    "Actin_accumulation_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Progressive_scapulohumeroperoneal_distal_myopathy": 1,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion|Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Familial_restrictive_cardiomyopathy|Nemaline_myopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|not_provided|Familial_restrictive_cardiomyopathy|Actin_accumulation_myopathy|Alpha-actinopathy": 1,
    "not_provided|NUP133-related_disorder": 11,
    "NUP133-related_disorder|not_provided": 12,
    "Nephrotic_syndrome|_type_18|not_specified|not_provided": 1,
    "Galloway-Mowat_syndrome_8": 3,
    "Nephrotic_syndrome|_type_18": 6,
    "NUP133-related_disorder": 10,
    "Nephrotic_syndrome|_type_18|not_provided": 1,
    "not_provided|not_specified|focal_and_segmental_glomerulosclerosis|Galloway-Mowat_syndrome": 1,
    "not_specified|not_provided|NUP133-related_disorder": 1,
    "not_provided|Galloway-Mowat_syndrome_8|Nephrotic_syndrome|_type_18": 1,
    "Galloway-Mowat_syndrome_8|Nephrotic_syndrome|_type_18": 1,
    "Congenital_disorder_of_glycosylation|_type_iit": 9,
    "not_provided|GALNT2-related_disorder": 4,
    "GALNT2-related_disorder|not_provided": 4,
    "not_provided|Congenital_disorder_of_glycosylation|_type_iit": 1,
    "Congenital_disorder_of_glycosylation|_type_iit|not_provided": 2,
    "GALNT2-related_disorder|Congenital_disorder_of_glycosylation|_type_iit|not_provided": 1,
    "GALNT2-related_disorder": 1,
    "Congenital_disorder_of_glycosylation|_type_IIq": 94,
    "not_specified|Congenital_disorder_of_glycosylation|_type_IIq": 8,
    "Congenital_disorder_of_glycosylation|_type_IIq|not_specified": 7,
    "not_provided|Congenital_disorder_of_glycosylation|_type_IIq": 5,
    "COG2-related_disorder|Congenital_disorder_of_glycosylation|_type_IIq|not_specified": 1,
    "COG2-related_disorder|Congenital_disorder_of_glycosylation|_type_IIq|not_provided": 3,
    "Congenital_disorder_of_glycosylation|_type_IIq|not_provided": 6,
    "not_provided|not_specified|Congenital_disorder_of_glycosylation|_type_IIq": 1,
    "not_specified|Congenital_disorder_of_glycosylation|_type_IIq|not_provided": 1,
    "not_provided|COG2-related_disorder|Congenital_disorder_of_glycosylation|_type_IIq": 1,
    "COG2-related_disorder|Congenital_disorder_of_glycosylation|_type_IIq": 2,
    "Renal_tubular_dysgenesis|not_provided": 34,
    "not_provided|Renal_tubular_dysgenesis": 30,
    "AGT-related_disorder|Renal_tubular_dysgenesis|not_provided": 2,
    "Renal_tubular_dysgenesis_of_genetic_origin": 68,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin": 13,
    "Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 10,
    "not_provided|Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin": 11,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|AGT-related_disorder|Renal_tubular_dysgenesis|not_provided": 1,
    "not_provided|Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 2,
    "Anhydramnios|Large_fontanelles": 2,
    "not_provided|AGT-related_disorder|Renal_tubular_dysgenesis": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 2,
    "AGT-related_disorder|not_provided": 2,
    "AGT-related_disorder|not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 1,
    "not_specified|not_provided|Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 1,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 4,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis|not_provided": 3,
    "not_provided|Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|AGT-related_disorder": 1,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 5,
    "AGT-related_disorder|Renal_tubular_dysgenesis": 1,
    "not_provided|Renal_tubular_dysgenesis|not_specified": 7,
    "Hypertensive_disorder|Renal_tubular_dysgenesis|not_specified|not_provided|Hypertension|_essential|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Renal_tubular_dysgenesis_of_genetic_origin": 2,
    "AGT-related_disorder": 2,
    "not_provided|Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|AGT-related_disorder|Renal_tubular_dysgenesis": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|not_provided": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|AGT-related_disorder": 2,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic": 2,
    "Inborn_genetic_diseases|Renal_tubular_dysgenesis|not_provided": 1,
    "AGT-related_disorder|Inborn_genetic_diseases|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "AGT-related_disorder|Renal_tubular_dysgenesis|not_specified|not_provided": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|Anhydramnios": 1,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 1,
    "Renal_tubular_dysgenesis|Hypertension|_essential|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 1,
    "ARV1-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_38": 10,
    "not_provided|ARV1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|ARV1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_38|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_38": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_38": 1,
    "ARV1-related_disorder|Developmental_and_epileptic_encephalopathy|_38": 1,
    "not_provided|ARV1-related_disorder": 2,
    "3-methylglutaconic_aciduria|_type_VIIB|Developmental_and_epileptic_encephalopathy|_38|not_provided": 1,
    "Abnormality_of_the_nervous_system|Blindness|Neurodegeneration|Developmental_and_epileptic_encephalopathy|_38": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB": 24,
    "not_provided|See_cases|Inborn_genetic_diseases": 6,
    "Developmental_and_epileptic_encephalopathy|_38|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|ARV1-related_disorder|Developmental_and_epileptic_encephalopathy|_38": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_2": 58,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_2": 10,
    "Rhizomelic_chondrodysplasia_punctata_type_2|not_provided": 25,
    "not_specified|Rhizomelic_chondrodysplasia_punctata_type_2|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_2|not_provided|not_specified": 4,
    "Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_2": 2,
    "Inborn_genetic_diseases|not_provided|Rhizomelic_chondrodysplasia_punctata_type_2": 2,
    "not_specified|not_provided|Rhizomelic_chondrodysplasia_punctata_type_2": 2,
    "not_provided|not_specified|Rhizomelic_chondrodysplasia_punctata_type_2": 3,
    "Rhizomelic_chondrodysplasia_punctata_type_2|Inborn_genetic_diseases": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_2|Rhizomelic_chondrodysplasia_punctata": 1,
    "not_specified|Rhizomelic_chondrodysplasia_punctata_type_2": 1,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_2|not_specified": 2,
    "not_provided|GNPAT-related_disorder": 2,
    "Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_2|not_provided": 3,
    "Rhizomelic_chondrodysplasia_punctata_type_2|GNPAT-related_disorder|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_2|not_provided|Rhizomelic_chondrodysplasia_punctata|not_specified": 1,
    "Rhizomelic_chondrodysplasia_punctata|not_provided": 6,
    "GNPAT-related_disorder|not_provided|Rhizomelic_chondrodysplasia_punctata_type_2": 1,
    "Rhizomelic_chondrodysplasia_punctata": 53,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_brain_atrophy": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_brain_atrophy|not_provided": 2,
    "not_provided|EXOC8-related_disorder|Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_brain_atrophy": 1,
    "Joubert_syndrome": 1512,
    "Progeroid_features-hepatocellular_carcinoma_predisposition_syndrome": 2,
    "Progeroid_features-hepatocellular_carcinoma_predisposition_syndrome|not_provided": 2,
    "Progeroid_features-hepatocellular_carcinoma_predisposition_syndrome|not_provided|SPRTN-related_disorder": 1,
    "SPRTN-related_disorder|not_provided": 1,
    "SPRTN-related_disorder": 1,
    "Erythrocytosis|_familial|_3": 223,
    "Familial_erythrocytosis": 30,
    "Erythrocytosis|_familial|_3|not_specified": 111,
    "not_specified|Erythrocytosis|_familial|_3": 121,
    "not_specified|not_provided|Erythrocytosis|_familial|_3": 8,
    "Familial_erythrocytosis|not_provided": 3,
    "Erythrocytosis|_familial|_3|EGLN1-related_disorder": 1,
    "Erythrocytosis|_familial|_3|Hemoglobin|_high_altitude_adaptation": 2,
    "not_provided|not_specified|Erythrocytosis|_familial|_3": 5,
    "not_specified|Erythrocytosis|_familial|_3|not_provided": 4,
    "Erythrocytosis|_familial|_3|not_provided": 7,
    "Erythrocytosis|_familial|_3|not_specified|not_provided": 2,
    "Erythrocytosis|_familial|_3|not_provided|not_specified": 3,
    "not_specified|Hemoglobin|_high_altitude_adaptation|Erythrocytosis|_familial|_3|not_provided": 1,
    "not_provided|Erythrocytosis|_familial|_3|not_specified": 3,
    "not_specified|Erythrocytosis|_familial|_3|Hemoglobin|_high_altitude_adaptation": 2,
    "not_specified|EGLN1-related_disorder|Erythrocytosis|_familial|_3": 1,
    "Erythrocytosis|_familial|_3|Hemoglobin|_high_altitude_adaptation|not_specified": 4,
    "Erythrocytosis|_familial|_3|Hemoglobin|_high_altitude_adaptation|not_provided|not_specified": 1,
    "EGLN1-related_disorder": 2,
    "not_specified|EGLN1-related_disorder|Erythrocytosis|_familial|_3|Hemoglobin|_high_altitude_adaptation|not_provided": 1,
    "Erythrocytosis|_familial|_3|Hemoglobin|_high_altitude_adaptation|not_provided": 1,
    "not_provided|EGLN1-related_disorder|not_specified|Erythrocytosis|_familial|_3": 1,
    "not_specified|EGLN1-related_disorder": 1,
    "not_provided|Erythrocytosis|_familial|_3": 6,
    "not_provided|Familial_erythrocytosis": 5,
    "DISC1-related_disorder": 20,
    "DISC1-related_disorder|not_provided|not_specified": 1,
    "DISC1-related_disorder|not_provided": 6,
    "not_provided|DISC1-related_disorder": 5,
    "not_specified|DISC1-related_disorder": 1,
    "DISC1-related_disorder|not_specified": 1,
    "COA6-related_disorder": 1,
    "not_provided|not_specified|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_4": 1,
    "COA6-related_disorder|not_specified|not_provided": 1,
    "not_specified|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_4|not_provided": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_4": 4,
    "COA6-related_disorder|not_provided": 1,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_4": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_4|not_provided": 1,
    "Immune_deficiency|_familial_variable": 1,
    "Varicella|_severe_recurrent": 1,
    "Immunodeficiency|_common_variable|_14": 11,
    "IRF2BP2-related_disorder|not_provided": 12,
    "not_provided|IRF2BP2-related_disorder": 7,
    "IRF2BP2-related_disorder|not_specified|not_provided": 1,
    "IRF2BP2-related_disorder": 3,
    "not_provided|Immunodeficiency|_common_variable|_14|not_specified": 1,
    "Immunodeficiency|_common_variable|_14|not_provided": 3,
    "not_provided|Immunodeficiency|_common_variable|_14": 10,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_14": 1,
    "not_provided|IRF2BP2-related_disorder|not_specified": 1,
    "Inborn_error_of_immunity": 1,
    "IRF2BP2-related_disorder|Immunodeficiency|_common_variable|_14|not_provided": 2,
    "Immunodeficiency|_common_variable|_14|not_specified|not_provided": 2,
    "not_provided|Immunodeficiency|_common_variable|_14|IRF2BP2-related_disorder": 1,
    "Muscular_dystrophy|_congenital_hearing_loss|_and_ovarian_insufficiency_syndrome|not_provided": 1,
    "Muscular_dystrophy|_congenital_hearing_loss|_and_ovarian_insufficiency_syndrome": 7,
    "Myopathy|Sensorineural_hearing_loss_disorder": 1,
    "Myopathy|Sensorineural_hearing_loss_disorder|Premature_ovarian_insufficiency|Muscular_dystrophy|_congenital_hearing_loss|_and_ovarian_insufficiency_syndrome|not_provided": 1,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome": 17,
    "not_provided|Hypoparathyroidism-retardation-dysmorphism_syndrome": 15,
    "not_provided|TBCE-related_disorder": 3,
    "Autosomal_recessive_Kenny-Caffey_syndrome|Hypoparathyroidism-retardation-dysmorphism_syndrome|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy": 6,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome|not_provided": 12,
    "not_provided|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Autosomal_recessive_Kenny-Caffey_syndrome|Hypoparathyroidism-retardation-dysmorphism_syndrome|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_Kenny-Caffey_syndrome|TBCE-related_disorder|not_provided|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Hypoparathyroidism-retardation-dysmorphism_syndrome|Disorder_of_sexual_differentiation": 1,
    "TBCE-related_disorder|not_provided": 5,
    "not_specified|not_provided|Hypoparathyroidism-retardation-dysmorphism_syndrome": 2,
    "Autosomal_recessive_Kenny-Caffey_syndrome|Hypoparathyroidism-retardation-dysmorphism_syndrome|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|not_provided": 2,
    "TBCE-related_disorder|Hypoparathyroidism-retardation-dysmorphism_syndrome|Autosomal_recessive_Kenny-Caffey_syndrome|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|not_provided": 1,
    "Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|TBCE-related_disorder|not_provided|Autosomal_recessive_Kenny-Caffey_syndrome|Hypoparathyroidism-retardation-dysmorphism_syndrome": 1,
    "not_specified|Hypoparathyroidism-retardation-dysmorphism_syndrome|not_provided": 2,
    "not_provided|not_specified|TBCE-related_disorder": 1,
    "TBCE-related_disorder|not_specified|not_provided|Hypoparathyroidism-retardation-dysmorphism_syndrome": 1,
    "TBCE-related_disorder|Hypoparathyroidism-retardation-dysmorphism_syndrome|not_provided": 1,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome|not_provided|not_specified": 1,
    "Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy": 5,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome|Autosomal_recessive_Kenny-Caffey_syndrome": 1,
    "Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Hypoparathyroidism-retardation-dysmorphism_syndrome|Autosomal_recessive_Kenny-Caffey_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Hypoparathyroidism-retardation-dysmorphism_syndrome": 1,
    "TBCE-related_disorder|not_provided|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy": 1,
    "Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|TBCE-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Autosomal_recessive_Kenny-Caffey_syndrome|Hypoparathyroidism-retardation-dysmorphism_syndrome": 1,
    "not_provided|Hypoparathyroidism-retardation-dysmorphism_syndrome|not_specified": 2,
    "TBCE-related_disorder": 2,
    "Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Hypoparathyroidism-retardation-dysmorphism_syndrome|Autosomal_recessive_Kenny-Caffey_syndrome": 2,
    "not_specified|not_provided|Autosomal_recessive_Kenny-Caffey_syndrome": 1,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome|Autosomal_recessive_Kenny-Caffey_syndrome|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|Inborn_genetic_diseases|not_provided": 1,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome|Autosomal_recessive_Kenny-Caffey_syndrome|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|not_provided": 2,
    "not_provided|TBCE-related_disorder|Hypoparathyroidism-retardation-dysmorphism_syndrome": 1,
    "Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy|not_provided|TBCE-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Encephalopathy|_progressive|_with_amyotrophy_and_optic_atrophy": 1,
    "Hypoparathyroidism-retardation-dysmorphism_syndrome|Microcephaly|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_Kenny-Caffey_syndrome": 1,
    "not_specified|TBCE-related_disorder|not_provided|Hypoparathyroidism-retardation-dysmorphism_syndrome": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 322,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|Inborn_genetic_diseases": 12,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 18,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided": 16,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 20,
    "B3GALNT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 2,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided": 3,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 5,
    "not_specified|B3GALNT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided": 1,
    "B3GALNT2-related_disorder": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided|Inborn_genetic_diseases": 3,
    "B3GALNT2-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 5,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_specified": 2,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|B3GALNT2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11": 2,
    "B3GALNT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|Muscular_dystrophy-dystroglycanopathy": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|B3GALNT2-related_disorder": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided|not_specified": 1,
    "B3GALNT2-related_disorder|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_11|not_provided": 1,
    "Ch\u00e9diak-Higashi_syndrome": 2863,
    "not_provided|Ch\u00e9diak-Higashi_syndrome": 58,
    "LYST-related_disorder|Ch\u00e9diak-Higashi_syndrome|not_specified": 1,
    "Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases": 71,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder": 2,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome": 102,
    "Ch\u00e9diak-Higashi_syndrome|not_provided": 50,
    "Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|not_provided": 1,
    "Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|not_specified": 1,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|not_specified": 2,
    "LYST-related_disorder|Ch\u00e9diak-Higashi_syndrome": 18,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|not_provided": 6,
    "Adrenocortical_carcinoma|_hereditary|Ch\u00e9diak-Higashi_syndrome": 1,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|not_provided|LYST-related_disorder": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_specified|not_provided": 6,
    "not_specified|Ch\u00e9diak-Higashi_syndrome": 21,
    "Ch\u00e9diak-Higashi_syndrome|not_specified": 17,
    "Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome": 9,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|LYST-related_disorder": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 6,
    "Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome": 7,
    "Inborn_genetic_diseases|Meniere_disease|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Ch\u00e9diak-Higashi_syndrome": 4,
    "Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder": 21,
    "LYST-related_disorder": 14,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases": 5,
    "LYST-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "Autoinflammatory_syndrome": 211,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|not_specified": 9,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|not_provided": 9,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder": 1,
    "Spastic_ataxia|Ch\u00e9diak-Higashi_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|CHEDIAK-HIGASHI_SYNDROME|_CHILDHOOD_TYPE": 5,
    "Inborn_genetic_diseases|LYST-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Ch\u00e9diak-Higashi_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Ch\u00e9diak-Higashi_syndrome": 8,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|not_provided": 10,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome|Abnormal_bleeding|Thrombocytopenia": 1,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|not_specified|Thrombocytopenia|Abnormal_bleeding": 1,
    "LYST-related_disorder|not_specified|Autoinflammatory_syndrome|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|LYST-related_disorder|Ch\u00e9diak-Higashi_syndrome": 2,
    "LYST-related_disorder|Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome": 1,
    "not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 9,
    "not_provided|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|not_specified": 2,
    "Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "LYST-related_disorder|not_specified|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome": 5,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|Ch\u00e9diak-Higashi_syndrome": 1,
    "LYST-related_disorder|Autoinflammatory_syndrome|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 2,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|not_provided|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome": 3,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Ch\u00e9diak-Higashi_syndrome": 9,
    "Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|LYST-related_disorder": 1,
    "not_provided|not_specified|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome": 2,
    "Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|not_provided": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|not_specified|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|not_specified|Ch\u00e9diak-Higashi_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|LYST-related_disorder|not_provided|Ch\u00e9diak-Higashi_syndrome": 2,
    "Autoinflammatory_syndrome|LYST-related_disorder|Meniere_disease|Inborn_genetic_diseases|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "LYST-related_disorder|Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|not_specified": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|not_specified": 3,
    "Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|not_specified|not_provided": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_specified|not_provided|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Ch\u00e9diak-Higashi_syndrome|not_specified": 1,
    "Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|not_specified|not_provided|LYST-related_disorder": 1,
    "LYST-related_disorder|not_provided|Ch\u00e9diak-Higashi_syndrome": 3,
    "LYST-related_disorder|not_specified|Ch\u00e9diak-Higashi_syndrome|not_provided": 1,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome": 1,
    "Susceptibility_to_severe_COVID-19|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "CHEDIAK-HIGASHI_SYNDROME|_ADULT_TYPE|Ch\u00e9diak-Higashi_syndrome": 2,
    "not_provided|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|Spastic_ataxia": 1,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|not_provided": 1,
    "LYST-related_disorder|Autoinflammatory_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|not_specified": 1,
    "Autoinflammatory_syndrome|not_specified|Ch\u00e9diak-Higashi_syndrome": 1,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|not_provided|LYST-related_disorder|Autoinflammatory_syndrome|Meniere_disease": 1,
    "not_provided|LYST-related_disorder|Ch\u00e9diak-Higashi_syndrome": 2,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|Inborn_genetic_diseases": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|Spastic_ataxia": 1,
    "Ch\u00e9diak-Higashi_syndrome|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_specified|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 2,
    "Ch\u00e9diak-Higashi_syndrome|not_specified|Inborn_genetic_diseases": 3,
    "LYST-related_disorder|Autoinflammatory_syndrome|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Ch\u00e9diak-Higashi_syndrome|not_specified|Autoinflammatory_syndrome": 1,
    "not_specified|Autoinflammatory_syndrome|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|Meniere_disease": 1,
    "CHEDIAK-HIGASHI_SYNDROME|_ADULT_TYPE|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|CHEDIAK-HIGASHI_SYNDROME|_CHILDHOOD_TYPE": 1,
    "not_provided|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Autoinflammatory_syndrome|Ch\u00e9diak-Higashi_syndrome": 1,
    "Recurrent_infections|Ch\u00e9diak-Higashi_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|not_provided|LYST-related_disorder|Autoinflammatory_syndrome": 1,
    "not_provided|LYST-related_disorder|Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome": 1,
    "LYST-related_disorder|Ch\u00e9diak-Higashi_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Ch\u00e9diak-Higashi_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Ch\u00e9diak-Higashi_syndrome|Autoinflammatory_syndrome": 2,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|not_specified": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_specified|Autoinflammatory_syndrome|not_provided": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_specified|LYST-related_disorder": 1,
    "Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases|LYST-related_disorder": 2,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome": 2,
    "Inborn_genetic_diseases|Ch\u00e9diak-Higashi_syndrome|Optic_neuropathy": 1,
    "Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|not_provided": 1,
    "Autoinflammatory_syndrome|not_provided|Ch\u00e9diak-Higashi_syndrome|Inborn_genetic_diseases": 1,
    "Ch\u00e9diak-Higashi_syndrome|not_provided|LYST-related_disorder|Autoinflammatory_syndrome": 1,
    "CHEDIAK-HIGASHI_SYNDROME|_CHILDHOOD_TYPE|Ch\u00e9diak-Higashi_syndrome": 1,
    "Inborn_genetic_diseases|Meniere_disease|Ch\u00e9diak-Higashi_syndrome": 1,
    "Ch\u00e9diak-Higashi_syndrome|LYST-related_disorder|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_specified|Ch\u00e9diak-Higashi_syndrome|not_provided": 1,
    "Focal_epilepsy|Hemiparesis|Hydrocephalus": 1,
    "not_specified|Hypohidrotic_ectodermal_dysplasia|Hypohidrotic_Ectodermal_Dysplasia|_Recessive|not_provided": 1,
    "Inborn_genetic_diseases|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant": 2,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|not_specified|not_provided|Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 21,
    "Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_specified|Hypohidrotic_ectodermal_dysplasia|not_provided": 1,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_provided": 5,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant": 3,
    "Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 5,
    "Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Hypohidrotic_ectodermal_dysplasia|Inborn_genetic_diseases": 1,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Hypohidrotic_ectodermal_dysplasia": 1,
    "Hypohidrotic_ectodermal_dysplasia": 57,
    "not_specified|Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_provided": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Hypohidrotic_ectodermal_dysplasia": 14,
    "not_provided|Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_specified|Ectodermal_dysplasia": 1,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 1,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|ECTODERMAL_DYSPLASIA_11B|_HYPOHIDROTIC/HAIR/TOOTH_TYPE|_AUTOSOMAL_DOMINANT": 1,
    "Hypohidrotic_ectodermal_dysplasia|not_provided|Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|not_specified": 1,
    "Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Hypohidrotic_ectodermal_dysplasia|EDARADD-related_disorder": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 11,
    "Tooth_agenesis": 10,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Ectodermal_dysplasia_11A|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Hypohidrotic_ectodermal_dysplasia|not_provided": 5,
    "Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Hypohidrotic_ectodermal_dysplasia|not_provided": 1,
    "Hypohidrotic_ectodermal_dysplasia|Hypohidrotic_Ectodermal_Dysplasia|_Recessive": 13,
    "Hypohidrotic_Ectodermal_Dysplasia|_Recessive": 5,
    "Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 13,
    "not_provided|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 2,
    "Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_provided": 3,
    "Hypohidrotic_ectodermal_dysplasia|Hypohidrotic_Ectodermal_Dysplasia|_Recessive|not_provided": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Recessive|not_provided|Hypohidrotic_ectodermal_dysplasia": 2,
    "not_provided|Hypohidrotic_ectodermal_dysplasia|Hypohidrotic_Ectodermal_Dysplasia|_Recessive": 1,
    "not_provided|Hypohidrotic_Ectodermal_Dysplasia|_Recessive|Hypohidrotic_ectodermal_dysplasia": 2,
    "Dilated_cardiomyopathy_1AA": 44,
    "not_provided|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1AA": 1,
    "Cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 134,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 516,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype": 36,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 79,
    "ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 8,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 7,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|Cardiovascular_phenotype": 2,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Intrinsic_cardiomyopathy|Cardiovascular_phenotype|ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 35,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 7,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Ventricular_fibrillation": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 14,
    "ACTN2-related_disorder": 10,
    "not_specified|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 3,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided": 13,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided": 3,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 17,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided": 2,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 12,
    "Intrinsic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 15,
    "not_provided|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities": 6,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|ACTN2-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 28,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|ACTN2-related_disorder": 2,
    "Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiomyopathy|_familial_hypertrophic|_23|_with_or_without_ventricular_noncompaction": 1,
    "Cardiovascular_phenotype|not_specified|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 3,
    "Cardiovascular_phenotype|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|ACTN2-related_disorder|Cardiomyopathy|_familial_hypertrophic|_23|_with_or_without_ventricular_noncompaction|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 5,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 7,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Cardiovascular_phenotype|not_provided|not_specified|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Myopathy|_distal|_6|_adult-onset|_autosomal_dominant": 4,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided": 17,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 3,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Long_QT_syndrome": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype": 5,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|ACTN2-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|Cardiovascular_phenotype": 2,
    "not_specified|ACTN2-related_disorder|not_provided": 1,
    "not_provided|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 6,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 4,
    "not_specified|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|not_specified|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified": 6,
    "Cardiomyopathy|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|not_provided": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|not_specified|not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "not_provided|Dilated_cardiomyopathy_1AA": 3,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|ACTN2-related_disorder|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided": 3,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiomyopathy": 8,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|ACTN2-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy": 4,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Syncope|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 4,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 2,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 4,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype": 3,
    "not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "not_specified|ACTN2-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|ACTN2-related_disorder": 1,
    "Cardiovascular_phenotype|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|ACTN2-related_disorder|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Hypertrophic_cardiomyopathy": 2,
    "ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Intrinsic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "ACTN2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "ACTN2-related_disorder|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Hypertrophic_cardiomyopathy_1": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiomyopathy": 6,
    "not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic|_23|_with_or_without_ventricular_noncompaction|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_provided": 5,
    "not_specified|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Central_core_myopathy|Cardiovascular_phenotype|ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Neuromuscular_disease|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiomyopathy": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Left_ventricular_noncompaction_1": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided|Congestive_heart_failure": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|ACTN2-related_disorder": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ACTN2-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|ACTN2-related_disorder|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_hypertrophic|_23|_with_or_without_ventricular_noncompaction": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_specified": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Tetralogy_of_Fallot|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ACTN2-related_disorder|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|not_specified|ACTN2-related_disorder": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 1,
    "Intrinsic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Wolff-Parkinson-White_pattern|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ACTN2-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "ACTN2-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|ACTN2-related_disorder|not_provided|Cardiomyopathy": 1,
    "Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|Cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|ACTN2-related_disorder|not_provided": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|not_provided": 5,
    "Cardiovascular_phenotype|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|ACTN2-related_disorder|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|not_provided": 1,
    "Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|Intrinsic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_provided": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|ACTN2-related_disorder|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Dilated_cardiomyopathy_1AA|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1AA|Primary_familial_hypertrophic_cardiomyopathy|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ACTN2-related_disorder|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1AA|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1AA|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy": 237,
    "not_provided|Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant": 1,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant": 5,
    "Dilated_cardiomyopathy_1AA|Myopathy|_congenital|_with_structured_cores_and_z-line_abnormalities|Myopathy|_distal|_6|_adult-onset|_autosomal_dominant|not_provided": 1,
    "Methylcobalamin_deficiency_type_cblG": 813,
    "Methylcobalamin_deficiency_type_cblG|not_provided|Inborn_genetic_diseases": 1,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 3,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism": 11,
    "not_specified|Methylcobalamin_deficiency_type_cblG": 12,
    "Methylcobalamin_deficiency_type_cblG|not_provided": 14,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblG": 7,
    "MTR-related_disorder": 4,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylcobalamin_deficiency_type_cblG|Intellectual_disability": 1,
    "not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 1,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|Neural_tube_defects|_folate-sensitive|not_specified|not_provided": 1,
    "Methylcobalamin_deficiency_type_cblG|not_specified": 10,
    "Methylcobalamin_deficiency_type_cblG|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 3,
    "Methylcobalamin_deficiency_type_cblG|Inborn_genetic_diseases": 18,
    "Homocystinuria|Decreased_methionine_synthase_activity": 1,
    "MTR-related_disorder|Methylcobalamin_deficiency_type_cblG": 2,
    "Methylcobalamin_deficiency_type_cblG|See_cases|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|not_specified|Methylcobalamin_deficiency_type_cblG": 4,
    "not_provided|Methylcobalamin_deficiency_type_cblG": 13,
    "Methylcobalamin_deficiency_type_cblG|Neural_tube_defects|_folate-sensitive": 7,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblG|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|MTR-related_disorder|Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblG|not_specified|MTR-related_disorder": 1,
    "Methylcobalamin_deficiency_type_cblG|not_specified|not_provided": 2,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Methylcobalamin_deficiency_type_cblG": 1,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|MTR-related_disorder": 1,
    "Methylcobalamin_deficiency_type_cblG|Intellectual_disability": 1,
    "Methylcobalamin_deficiency_type_cblG|MTR-related_disorder": 3,
    "not_provided|Methylcobalamin_deficiency_type_cblG|Inborn_genetic_diseases": 1,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided": 2,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|MTR-related_disorder|Methylcobalamin_deficiency_type_cblG": 1,
    "not_specified|not_provided|Methylcobalamin_deficiency_type_cblG": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|Methylcobalamin_deficiency_type_cblG": 1,
    "not_provided|not_specified|Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 2,
    "not_provided|Methylcobalamin_deficiency_type_cblG|MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblG|Neural_tube_defects|_folate-sensitive|not_specified": 1,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblG|not_provided": 2,
    "Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblG": 5,
    "not_specified|Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 1,
    "not_provided|Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblG": 2,
    "not_specified|Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblG": 1,
    "Methylcobalamin_deficiency_type_cblG|Neural_tube_defects|_folate-sensitive|Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|MTR-related_disorder|not_provided": 1,
    "not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 2,
    "See_cases|Methylcobalamin_deficiency_type_cblG": 1,
    "Methylcobalamin_deficiency_type_cblG|not_provided|Intellectual_disability|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblG|not_provided|not_specified": 1,
    "Methylcobalamin_deficiency_type_cblG|not_provided|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism": 2,
    "not_specified|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 1,
    "MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Gastrointestinal_stromal_tumor|Methylcobalamin_deficiency_type_cblG|Neural_tube_defects|_folate-sensitive|_susceptibility_to": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|not_specified|MTR-related_disorder|Methylcobalamin_deficiency_type_cblG": 1,
    "MTR-related_disorder|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 1,
    "Intellectual_disability|Methylcobalamin_deficiency_type_cblG": 1,
    "Methylcobalamin_deficiency_type_cblG|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|Methylcobalamin_deficiency_type_cblG|See_cases|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylcobalamin_deficiency_type_cblG": 1,
    "MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG|not_specified": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|MTR-related_disorder|not_provided|Methylcobalamin_deficiency_type_cblG": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG|Inborn_genetic_diseases|not_provided": 1,
    "Methylcobalamin_deficiency_type_cblG|MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "MTR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG|Neural_tube_defects|_folate-sensitive|not_specified|not_provided": 1,
    "not_provided|Methylcobalamin_deficiency_type_cblG|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|not_specified": 1,
    "not_provided|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG": 1,
    "Methylcobalamin_deficiency_type_cblG|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG|Epilepsy|Intellectual_disability|_profound|Decreased_methionine_synthase_activity|Homocystinuria|MTR-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|Methylcobalamin_deficiency_type_cblG|not_specified": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|not_specified|Methylcobalamin_deficiency_type_cblG": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylcobalamin_deficiency_type_cblG": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblG|Neural_tube_defects|_folate-sensitive|not_provided|MTR-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Methylcobalamin_deficiency_type_cblG|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 8,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy": 16,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 132,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 40,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 11,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 8,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 16,
    "not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 21,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 22,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 11,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 41,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 9,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 9,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 3,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 22,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 13,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 161,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 41,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 129,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 63,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 106,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 4,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 11,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 11,
    "Conduction_disorder_of_the_heart": 5,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 13,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 26,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified": 9,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 52,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 6,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype": 9,
    "not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 35,
    "Long_QT_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiac_arrest": 8,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 33,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 22,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 16,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 4,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 5,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|not_specified": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_provided|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 14,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 15,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 11,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 13,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 5,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 7,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 13,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 2,
    "Cardiomyopathy|RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 20,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 41,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "RYR2-related_disorder": 8,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 8,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 7,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 7,
    "not_provided|RYR2-related_disorder": 1,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 43,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "RYR2-related_disorder|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 19,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 20,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|not_provided": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 16,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 9,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 6,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Wolff-Parkinson-White_pattern": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 4,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 3,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 8,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 3,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 5,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "not_specified|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_fibrillation|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 4,
    "Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Long_QT_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 14,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 9,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 3,
    "Cardiomyopathy|not_provided|Cardiac_arrhythmia|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 36,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_tachycardia|not_specified|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 13,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "not_provided|Cardiac_arrhythmia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 12,
    "Cardiovascular_phenotype|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 6,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "RYR2-related_disorder|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 8,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 13,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Primary_dilated_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 8,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 5,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 2,
    "Syncope|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 4,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 5,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiomyopathy": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 6,
    "Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 9,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Long_QT_syndrome|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Sudden_death|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 3,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiac_arrhythmia": 1,
    "not_specified|Cardiomyopathy": 49,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 4,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "RYR2-related_disorder|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Cardiomyopathy": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Diastolic_dysfunction|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 11,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Wolff-Parkinson-White_pattern|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 5,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 4,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 13,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Wolff-Parkinson-White_pattern|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Primary_dilated_cardiomyopathy|not_provided|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Death_in_infancy|not_provided|Cardiomyopathy": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 6,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Sudden_unexplained_death|Sudden_cardiac_death|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 9,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 5,
    "Dilated_cardiomyopathy_1C|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype": 6,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 3,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 2,
    "Wolff-Parkinson-White_pattern|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 12,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 4,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Cardiac_arrhythmia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_1": 6,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder": 1,
    "not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified": 3,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 5,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified": 3,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy": 402,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 2,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 10,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 3,
    "not_specified|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Wolff-Parkinson-White_pattern|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "RYR2-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Hypertrophic_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_1|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome": 1,
    "not_provided|Cardiomyopathy|Premature_coronary_artery_atherosclerosis|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|RYR2-related_disorder|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome|Cardiomyopathy": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 4,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|RYR2-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Conduction_disorder_of_the_heart|not_specified": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Long_QT_syndrome": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiac_arrhythmia|Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 5,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Cardiomyopathy|RYR2-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Conduction_disorder_of_the_heart|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 8,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Heart_disease|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "RYR2-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Cardiovascular_phenotype|Conduction_disorder_of_the_heart|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 4,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 2,
    "not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 7,
    "not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 3,
    "RYR2-related_disorder|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|RYR2-related_disorder|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiac_arrhythmia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Cardiac_arrhythmia|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|Cardiomyopathy|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|RYR2-related_disorder|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Dilated_cardiomyopathy_with_left_ventricular_noncompaction|RYR2-related_disorder|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|not_provided": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|RYR2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Sudden_cardiac_arrest|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 4,
    "not_provided|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Long_QT_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified": 2,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_4": 100,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Sinus_bradycardia|Ventricular_hypertrophy|Left_ventricular_noncompaction_cardiomyopathy|Abnormal_trabecular_meshwork_morphology|Heart|_malformation_of|Prolonged_QTc_interval": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 41,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 2,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiac_arrhythmia|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Long_QT_syndrome|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 2,
    "RYR2-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "RYR2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Primary_familial_dilated_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|not_specified|RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|RYR2-related_disorder|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 2,
    "Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype": 10,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Congestive_heart_failure|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiac_arrhythmia|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Long_QT_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "not_provided|not_specified|Cardiomyopathy": 14,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|RYR2-related_disorder|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided": 1,
    "Sudden_unexplained_death|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiac_arrhythmia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 2,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Cardiomyopathy|Wolff-Parkinson-White_pattern|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "not_specified|Cardiac_arrhythmia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "RYR2-related_disorder|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Cardiomyopathy": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_provided|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Long_QT_syndrome": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Paroxysmal_familial_ventricular_fibrillation": 1,
    "not_specified|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|RYR2-related_disorder|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder": 1,
    "Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified": 1,
    "Primary_dilated_cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|RYR2-related_disorder|not_specified": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiomyopathy|RYR2-related_disorder|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiomyopathy|RYR2-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Hypertrophic_cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Left_ventricular_noncompaction|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Left_ventricular_noncompaction": 1,
    "RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_specified|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|RYR2-related_disorder|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiac_arrhythmia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiac_arrhythmia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Cardiomyopathy": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Cardiac_arrhythmia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_2|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided|Cardiac_arrhythmia": 1,
    "not_specified|not_provided|Cardiomyopathy": 17,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 5,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|RYR2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_2|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|not_provided|Cardiomyopathy": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_2|RYR2-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 5,
    "RYR2-related_disorder|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|not_specified": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Sudden_cardiac_death": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 1,
    "RYR2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiomyopathy": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|not_specified|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Ventricular_arrhythmias_due_to_cardiac_ryanodine_receptor_calcium_release_deficiency_syndrome|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Arrhythmogenic_right_ventricular_dysplasia_2|not_provided": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia": 5,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided": 1,
    "Prune_belly_syndrome": 40,
    "Prune_belly_syndrome|not_provided": 5,
    "not_provided|CHRM3-related_disorder": 2,
    "Prune_belly_syndrome|not_specified": 6,
    "not_provided|Prune_belly_syndrome": 3,
    "not_specified|Prune_belly_syndrome": 2,
    "CHRM3-related_disorder|not_provided": 1,
    "not_specified|Prune_belly_syndrome|not_provided": 1,
    "CHRM3-related_disorder": 2,
    "Prune_belly_syndrome|not_provided|not_specified": 2,
    "not_provided|not_specified|Prune_belly_syndrome": 1,
    "FMN2-related_disorder": 61,
    "Intellectual_disability|_autosomal_recessive_47": 28,
    "Aganglionic_megacolon|Intellectual_disability|_autosomal_recessive_47": 1,
    "FMN2-related_disorder|not_provided|not_specified": 2,
    "Intellectual_disability|_autosomal_recessive_47|not_provided": 8,
    "Intellectual_disability|_autosomal_recessive_47|not_specified|not_provided": 4,
    "FMN2-related_disorder|not_provided": 23,
    "Intellectual_disability|_autosomal_recessive_47|Inborn_genetic_diseases": 1,
    "FMN2-related_disorder|not_specified|not_provided": 3,
    "not_provided|FMN2-related_disorder": 40,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_47": 3,
    "Intellectual_disability|_autosomal_recessive_47|not_specified|FMN2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|FMN2-related_disorder": 1,
    "FMN2-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|FMN2-related_disorder": 2,
    "not_specified|not_provided|FMN2-related_disorder": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_47|FMN2-related_disorder": 1,
    "FMN2-related_disorder|not_provided|not_specified|Intellectual_disability|_autosomal_recessive_47": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_47": 2,
    "Intellectual_disability|_autosomal_recessive_47|FMN2-related_disorder|not_provided": 1,
    "not_specified|FMN2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_47|not_provided|Neurodevelopmental_abnormality|not_specified|FMN2-related_disorder": 1,
    "Tooth_agenesis|_selective|_9": 4,
    "GREM2-related_disorder": 1,
    "not_specified|Tooth_agenesis|_selective|_9": 1,
    "Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 9,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 4,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 7,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer": 78,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 39,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 41,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 25,
    "Fumarase_deficiency": 29,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 44,
    "Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 30,
    "Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Fumarase_deficiency|not_provided": 8,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 24,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 11,
    "Fumarase_deficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 13,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fumarase_deficiency": 24,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 21,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 28,
    "Hereditary_cancer-predisposing_syndrome|FH-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fumarase_deficiency": 1,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome": 29,
    "not_provided|Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome": 29,
    "not_provided|Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 6,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fumarase_deficiency": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder|Fumarase_deficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 3,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 4,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency": 8,
    "not_provided|Fumarase_deficiency": 13,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 67,
    "not_provided|Fumarase_deficiency|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_provided": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 4,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|FH-related_disorder": 2,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome": 15,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 2,
    "not_provided|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency": 10,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 5,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|FH-related_disorder|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder": 1,
    "FH-related_disorder|not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 2,
    "not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 4,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 3,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified|FH-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|FH-related_disorder": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "FH-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 73,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 6,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|not_provided": 14,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_provided|Hepatocellular_carcinoma": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Fumarase_deficiency": 2,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 2,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|not_provided": 1,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome": 4,
    "Fumarase_deficiency|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "FH-related_disorder|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 2,
    "Fumarase_deficiency|FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer|not_provided": 5,
    "Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 7,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 2,
    "not_specified|not_provided|Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 6,
    "not_provided|Fumarase_deficiency|not_specified|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 1,
    "Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|FH-related_disorder": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified|not_provided|Fumarase_deficiency": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_provided": 1,
    "not_provided|Fumarase_deficiency|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Fumarase_deficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|Spinocerebellar_ataxia_45|See_cases|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hepatoblastoma|Fumarase_deficiency|B_Lymphoblastic_Leukemia/Lymphoma|_Not_Otherwise_Specified": 1,
    "Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified": 1,
    "FH-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly": 1,
    "FH-related_disorder|not_provided": 1,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified|not_provided": 2,
    "Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Fumarase_deficiency": 1,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|FH-related_disorder|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 1,
    "Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Microcephaly|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|Uterine_leiomyoma|Cutaneous_leiomyoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided": 2,
    "FH-related_disorder|Hereditary_leiomyomatosis_and_renal_cell_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder|not_provided|not_specified": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|FH-related_disorder": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 45,
    "not_provided|Cutaneous_leiomyoma": 1,
    "Ovarian_cancer|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|not_specified": 1,
    "Fumarase_deficiency|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 76,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_provided|not_specified": 1,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer|Fumarase_deficiency|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Fumarase_deficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "not_provided|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|FH-related_disorder": 1,
    "Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Fumarase_deficiency": 1,
    "FH-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "FH-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fumarase_deficiency|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer|FH-related_disorder|Hereditary_cancer-predisposing_syndrome|Fumarase_deficiency": 1,
    "not_specified|FH-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "not_provided|FH-related_disorder|not_specified": 1,
    "not_specified|Fumarase_deficiency|not_provided|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Fumarase_deficiency|Hereditary_cancer-predisposing_syndrome|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "KMO-related_disorder": 1,
    "not_provided|EXO1-related_disorder": 3,
    "EXO1-related_disorder|not_provided": 4,
    "EXO1-related_disorder": 26,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|EXO1-related_disorder": 1,
    "EXO1-related_disorder|not_specified": 1,
    "not_provided|EXO1-related_disorder|not_specified": 1,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 191,
    "Bardet-Biedl_syndrome_16|not_provided|not_specified|Senior-Loken_syndrome_7": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 207,
    "SDCCAG8-related_disorder": 87,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder": 17,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|Inborn_genetic_diseases|SDCCAG8-related_disorder": 2,
    "SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 18,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 8,
    "SDCCAG8-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 4,
    "Inborn_genetic_diseases|SDCCAG8-related_disorder|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "SDCCAG8-related_disorder|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 31,
    "SDCCAG8-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|SDCCAG8-related_disorder": 17,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_provided": 8,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|Inborn_genetic_diseases": 5,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_provided|SDCCAG8-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 1,
    "not_specified|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder": 2,
    "not_specified|Senior-Loken_syndrome_7|not_provided|Bardet-Biedl_syndrome_16": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome|SDCCAG8-related_disorder|not_provided": 1,
    "not_specified|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder|Senior-Loken_syndrome_7|not_provided": 1,
    "Kidney_disorder|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|SDCCAG8-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 6,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_specified|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|Inborn_genetic_diseases": 10,
    "Bardet-Biedl_syndrome_16": 7,
    "Senior-Loken_syndrome_7|SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16": 3,
    "not_provided|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder": 2,
    "not_specified|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 1,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|Kidney_disorder": 1,
    "not_provided|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome|SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16": 1,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_provided|SDCCAG8-related_disorder": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|SDCCAG8-related_disorder|not_provided": 2,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_specified": 4,
    "Inborn_genetic_diseases|SDCCAG8-related_disorder": 4,
    "SDCCAG8-related_disorder|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|Bardet-Biedl_syndrome": 1,
    "SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_provided|Bardet-Biedl_syndrome": 1,
    "not_provided|Retinal_dystrophy|Kidney_disorder|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder|Senior-Loken_syndrome_7|not_specified": 1,
    "Bardet-Biedl_syndrome|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "Bardet-Biedl_syndrome_16|not_provided|Senior-Loken_syndrome_7": 1,
    "not_provided|Kidney_disorder|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_specified": 1,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_specified|not_provided": 1,
    "SDCCAG8-related_disorder|not_provided|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_specified": 1,
    "Bardet-Biedl_syndrome_16|not_provided|Senior-Loken_syndrome_7|SDCCAG8-related_disorder|not_specified": 1,
    "not_provided|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "not_specified|not_provided|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder|not_specified|not_provided": 1,
    "not_specified|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_provided|SDCCAG8-related_disorder": 1,
    "Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder|Senior-Loken_syndrome_7": 1,
    "Senior-Loken_syndrome_7|not_provided|not_specified|Bardet-Biedl_syndrome_16": 1,
    "SDCCAG8-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 1,
    "not_provided|SDCCAG8-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "SDCCAG8-related_disorder|Inborn_genetic_diseases|not_provided|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "SDCCAG8-related_disorder|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_7|not_provided": 1,
    "Senior-Loken_syndrome_7": 2,
    "not_provided|SDCCAG8-related_disorder|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "Senior-Loken_syndrome_7|SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 1,
    "not_provided|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|SDCCAG8-related_disorder": 1,
    "SDCCAG8-related_disorder|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_provided": 1,
    "Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome|not_provided": 1,
    "SDCCAG8-related_disorder|not_specified|not_provided|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|Kidney_disorder": 1,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder|not_specified|not_provided": 1,
    "not_specified|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|not_provided|SDCCAG8-related_disorder": 1,
    "Bardet-Biedl_syndrome_16|not_provided|Senior-Loken_syndrome_7|SDCCAG8-related_disorder": 1,
    "Senior-Loken_syndrome_7|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_16": 1,
    "Renal_dysplasia_and_retinal_aplasia": 5,
    "Bardet-Biedl_syndrome|SDCCAG8-related_disorder|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_provided": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7": 1,
    "not_provided|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_specified": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_16|Senior-Loken_syndrome_7|not_provided": 1,
    "SDCCAG8-related_disorder|not_provided|Inborn_genetic_diseases|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_7|Bardet-Biedl_syndrome_16|SDCCAG8-related_disorder": 1,
    "AKT3-related_disorder": 8,
    "Renal_dysplasia_and_retinal_aplasia|not_provided|Bardet-Biedl_syndrome": 1,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome": 2,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|not_provided": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 81,
    "not_provided|not_specified|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|not_provided": 8,
    "AKT3-related_disorder|Macrocephaly|Capillary_hemangioma|Global_developmental_delay|Polymicrogyria|Inborn_genetic_diseases|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|not_provided|See_cases": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|AKT3-related_disorder|not_provided": 1,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 3,
    "Inborn_genetic_diseases|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 3,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|not_specified": 3,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|AKT3-related_disorder": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|Inborn_genetic_diseases|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes": 1,
    "AKT3-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 1,
    "Seizure|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|not_provided": 1,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|not_specified|not_provided": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2": 1,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_2|Inborn_genetic_diseases": 1,
    "Renal_carnitine_transport_defect": 873,
    "Developmental_delay": 12,
    "Intellectual_disability|_autosomal_dominant_22": 42,
    "Intellectual_disability|_autosomal_dominant_22|not_provided": 11,
    "not_provided|ZBTB18-related_disorder": 2,
    "ZBTB18-related_disorder": 10,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_22": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_22|Inborn_genetic_diseases": 1,
    "ZBTB18-related_disorder|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_22|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_22": 6,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_22": 1,
    "Intellectual_disability|_autosomal_dominant_22|ZBTB18-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_22|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_22|Marfanoid_habitus_and_intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_22|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_22|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_22|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_22": 1,
    "ZBTB18-related_intellectual_disability": 2,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_22|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_22|not_provided|ZBTB18-related_disorder": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_11": 6,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11": 26,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_specified|not_provided": 1,
    "COX20-related_disorder|not_provided": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_provided": 6,
    "not_provided|Mitochondrial_disease|COX20-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_11|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_11": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_provided|Mitochondrial_disease": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_11": 1,
    "COX20-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_11": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|COX20-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_11|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Inborn_genetic_diseases": 1,
    "COX20-related_disorder|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_54": 739,
    "Developmental_and_epileptic_encephalopathy|_54|not_provided": 31,
    "Developmental_and_epileptic_encephalopathy|_54|Myoclonic_absence_seizure": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_54": 23,
    "Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases": 26,
    "Developmental_and_epileptic_encephalopathy|_54|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_54": 24,
    "Developmental_and_epileptic_encephalopathy|_54|See_cases": 1,
    "HNRNPU-related_disorder|Developmental_and_epileptic_encephalopathy|_54": 1,
    "Developmental_and_epileptic_encephalopathy|_54|Intellectual_disability_and_seizures": 1,
    "not_provided|Epileptic_encephalopathy": 142,
    "Developmental_and_epileptic_encephalopathy|_54|HNRNPU-related_disorder": 1,
    "not_provided|HNRNPU-related_disorder|Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases": 1,
    "HNRNPU-related_disorder": 7,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_54|not_provided": 4,
    "heterogeneous_nuclear_ribonucleoprotein_G|_human": 6,
    "Inborn_genetic_diseases|HNRNPU-related_disorder|Developmental_and_epileptic_encephalopathy|_54|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_54|not_specified": 4,
    "HNRNPU-related_developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases|not_specified": 2,
    "not_provided|Intellectual_disability|Seizure|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_54|heterogeneous_nuclear_ribonucleoprotein_G|_human": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases": 5,
    "Developmental_and_epileptic_encephalopathy|_54|not_provided|Inborn_genetic_diseases": 1,
    "HNRNPU-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases": 1,
    "not_provided|HNRNPU-related_disorder|Developmental_and_epileptic_encephalopathy|_54": 2,
    "Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases|not_provided": 2,
    "Epileptic_encephalopathy": 3548,
    "Developmental_and_epileptic_encephalopathy|_54|not_provided|Epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_54|HNRNPU-related_disorder|not_provided": 1,
    "Seizure|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_54|HNRNPU-related_disorder|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases|HNRNPU-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_54|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_54|not_provided|heterogeneous_nuclear_ribonucleoprotein_G|_human": 1,
    "Developmental_and_epileptic_encephalopathy|_1|not_provided": 3,
    "not_provided|Complex_neurodevelopmental_disorder": 19,
    "HNRNPU-related_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_54": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_54": 1,
    "Seizure|Intellectual_disability|Developmental_and_epileptic_encephalopathy|_54": 1,
    "KIF26B-related_disorder": 51,
    "not_provided|KIF26B-related_disorder": 14,
    "Autosomal_dominant_cerebellar_ataxia": 136,
    "KIF26B-related_disorder|not_provided": 13,
    "not_specified|KIF26B-related_disorder": 1,
    "KIF26B-related_disorder|not_specified": 1,
    "KIF26B-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|KIF26B-related_disorder": 1,
    "not_specified|KIF26B-related_disorder|not_provided": 2,
    "Autosomal_dominant_cerebellar_ataxia|not_provided": 37,
    "Strabismus|Intellectual_disability|Delayed_speech_and_language_development": 1,
    "Neurodevelopmental_disorders": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 10,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 2,
    "not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 6,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 9,
    "Familial_cold_autoinflammatory_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 3,
    "not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Autoinflammatory_syndrome|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "not_provided|Cryopyrin_associated_periodic_syndrome": 37,
    "not_provided|Inborn_genetic_diseases|NLRP3-related_disorder": 1,
    "Cryopyrin_associated_periodic_syndrome": 459,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "not_specified|Cryopyrin_associated_periodic_syndrome": 8,
    "Keratitis_fugax_hereditaria": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided": 37,
    "Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Cryopyrin_associated_periodic_syndrome": 2,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome": 2,
    "NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 37,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 4,
    "not_specified|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Cryopyrin_associated_periodic_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "not_specified|Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 3,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|not_specified|not_provided": 1,
    "NLRP3-related_disorder|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome": 7,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_specified": 2,
    "not_specified|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Long_COVID-19": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 2,
    "not_specified|Cryopyrin_associated_periodic_syndrome|not_provided": 2,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|not_specified|not_provided": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_provided|Autoinflammatory_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 1,
    "Cryopyrin_associated_periodic_syndrome|not_specified|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_provided": 9,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_1": 40,
    "Squamous_cell_carcinoma": 34,
    "not_provided|not_specified|Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Cryopyrin_associated_periodic_syndrome|not_specified|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Inborn_genetic_diseases|not_specified|not_provided|Cleft_palate": 1,
    "Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 5,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 2,
    "NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|not_provided": 2,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome": 2,
    "Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1": 14,
    "NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome": 4,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|not_specified|not_provided|Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder": 1,
    "Inborn_genetic_diseases|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 2,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 6,
    "not_specified|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 3,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Kidney_disorder|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome|NLRP3-related_disorder|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|not_specified|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|not_specified": 5,
    "not_provided|Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Inborn_genetic_diseases|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "NLRP3-associated_autoinflammatory_disease": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|not_provided|Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder": 3,
    "Cryopyrin_associated_periodic_syndrome|Keratitis_fugax_hereditaria|not_provided|not_specified|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Cryopyrin_associated_periodic_syndrome": 2,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "not_provided|Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|not_specified": 3,
    "Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|not_specified|Keratitis_fugax_hereditaria|not_provided": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_provided|not_specified": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 3,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Autoinflammatory_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|not_provided": 1,
    "not_provided|Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1": 6,
    "NLRP3-related_disorder|not_provided|not_specified|Cryopyrin_associated_periodic_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "not_provided|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|not_provided": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 1,
    "Kidney_disorder|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 5,
    "Inborn_genetic_diseases|Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria": 1,
    "NLRP3-related_disorder|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|not_provided|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "NLRP3-related_disorder|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|not_specified|not_provided": 2,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome": 4,
    "Inborn_genetic_diseases|not_specified|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Cryopyrin_associated_periodic_syndrome|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_1|not_provided": 2,
    "Cryopyrin_associated_periodic_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 2,
    "Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Focal_segmental_glomerulosclerosis": 1,
    "Autoinflammatory_syndrome|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "NLRP3-related_disorder|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome": 1,
    "Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Autoinflammatory_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "not_specified|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome": 1,
    "not_provided|Autoinflammatory_syndrome|not_specified|Cryopyrin_associated_periodic_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|not_provided": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_provided|not_specified|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder|Autoinflammatory_syndrome|Kidney_disorder|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|NLRP3-related_disorder|not_specified|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Inborn_genetic_diseases|Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 2,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Autoinflammatory_syndrome|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Hearing_impairment": 1,
    "Inborn_genetic_diseases|Cryopyrin_associated_periodic_syndrome": 3,
    "NLRP3-related_disorder": 4,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|not_provided": 1,
    "not_provided|Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome|not_provided": 2,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 2,
    "NLRP3-related_disorder|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Autoinflammatory_syndrome": 2,
    "not_provided|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 2,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Cryopyrin_associated_periodic_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|not_provided|Cryopyrin_associated_periodic_syndrome|not_specified": 1,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|NLRP3-related_disorder": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 3,
    "Pericardial_effusion|Pleural_effusion|Fever": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Autoinflammatory_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|NLRP3-related_disorder|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Cryopyrin_associated_periodic_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 3,
    "Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Focal_segmental_glomerulosclerosis": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "not_provided|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Cryopyrin_associated_periodic_syndrome": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|not_specified": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 1,
    "NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|not_specified|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 2,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|Autoinflammatory_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_provided|NLRP3-related_disorder": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|NLRP3-related_disorder": 1,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_specified": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_specified": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome": 1,
    "NLRP3-related_disorder|not_provided|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Cryopyrin_associated_periodic_syndrome": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|not_provided": 1,
    "not_provided|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Cryopyrin_associated_periodic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|not_provided": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|not_provided": 1,
    "not_provided|Cryopyrin_associated_periodic_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|NLRP3-related_disorder": 1,
    "not_provided|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Keratitis_fugax_hereditaria|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation": 1,
    "not_provided|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome": 1,
    "Cryopyrin_associated_periodic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1|Inborn_genetic_diseases|not_provided|Cryopyrin_associated_periodic_syndrome": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Familial_cold_autoinflammatory_syndrome_1|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|NLRP3-related_disorder": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Familial_cold_autoinflammatory_syndrome_1|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|NLRP3-related_disorder|Cryopyrin_associated_periodic_syndrome|not_specified": 1,
    "Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Keratitis_fugax_hereditaria|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Cryopyrin_associated_periodic_syndrome|Inborn_genetic_diseases": 1,
    "Cryopyrin_associated_periodic_syndrome|Hearing_loss|_autosomal_dominant_34|_with_or_without_inflammation|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Keratitis_fugax_hereditaria|Familial_amyloid_nephropathy_with_urticaria_AND_deafness|Familial_cold_autoinflammatory_syndrome_1": 1,
    "Familial_cold_autoinflammatory_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 3,
    "Autoinflammatory_syndrome|Cryopyrin_associated_periodic_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome|Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome_1|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "Chronic_infantile_neurological|_cutaneous_and_articular_syndrome|Familial_cold_autoinflammatory_syndrome|Familial_amyloid_nephropathy_with_urticaria_AND_deafness": 1,
    "OR2W3-related_disorder|not_provided": 3,
    "not_provided|OR2W3-related_disorder": 3,
    "Streaky_metaphyseal_sclerosis|Aplasia/Hypoplasia_of_the_phalanges_of_the_4th_toe": 4,
    "not_provided|ACP1_A/B_POLYMORPHISM": 1,
    "Gilbert_syndrome": 11,
    "Deficiency_of_iodide_peroxidase|not_provided": 24,
    "Deficiency_of_iodide_peroxidase": 69,
    "not_provided|not_specified|Deficiency_of_iodide_peroxidase": 5,
    "not_provided|Deficiency_of_iodide_peroxidase": 44,
    "Deficiency_of_iodide_peroxidase|Inborn_genetic_diseases": 2,
    "not_provided|TPO-related_disorder": 4,
    "Deficiency_of_iodide_peroxidase|TPO-related_disorder": 2,
    "TPO-related_disorder|Deficiency_of_iodide_peroxidase|not_provided": 2,
    "not_specified|Deficiency_of_iodide_peroxidase|not_provided": 3,
    "TPO-related_disorder|Hypothyroidism_due_to_TSH_receptor_mutations|Deficiency_of_iodide_peroxidase": 1,
    "TPO-related_disorder": 5,
    "Congenital_hypothyroidism": 23,
    "TPO-related_disorder|not_provided": 3,
    "Deficiency_of_iodide_peroxidase|not_provided|not_specified": 2,
    "not_provided|Deficiency_of_iodide_peroxidase|not_specified": 4,
    "TPO-related_disorder|not_provided|Deficiency_of_iodide_peroxidase": 2,
    "Deficiency_of_iodide_peroxidase|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Deficiency_of_iodide_peroxidase": 3,
    "Deficiency_of_iodide_peroxidase|Neurodevelopmental_disorder|not_provided": 1,
    "Deficiency_of_iodide_peroxidase|Short_stature|Delayed_speech_and_language_development|Congenital_hypothyroidism|Global_developmental_delay|Protruding_tongue|Intellectual_disability|_severe|Delayed_gross_motor_development": 1,
    "not_provided|Congenital_hypothyroidism": 5,
    "Inborn_genetic_diseases|not_provided|TPO-related_disorder": 1,
    "TPO-related_disorder|not_provided|not_specified|Deficiency_of_iodide_peroxidase": 1,
    "Deficiency_of_iodide_peroxidase|not_provided|TPO-related_disorder": 1,
    "not_specified|not_provided|Deficiency_of_iodide_peroxidase": 6,
    "Deficiency_of_iodide_peroxidase|not_specified": 1,
    "not_specified|Deficiency_of_iodide_peroxidase": 4,
    "Inborn_genetic_diseases|Deficiency_of_iodide_peroxidase|not_provided": 1,
    "Deficiency_of_iodide_peroxidase|Congenital_hypothyroidism": 1,
    "PXDN-related_disorder|not_provided|Anterior_segment_dysgenesis_7": 1,
    "Anterior_segment_dysgenesis_7": 141,
    "not_provided|Anterior_segment_dysgenesis_7": 19,
    "Anterior_segment_dysgenesis_7|not_provided": 17,
    "PXDN-related_disorder": 11,
    "Anterior_segment_dysgenesis_7|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Anterior_segment_dysgenesis_7": 3,
    "Anterior_segment_dysgenesis_7|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Anterior_segment_dysgenesis_7": 6,
    "not_specified|not_provided|Anterior_segment_dysgenesis_7": 2,
    "Anterior_segment_dysgenesis_7|not_provided|Anterior_segment_dysgenesis": 1,
    "not_provided|not_specified|Anterior_segment_dysgenesis_7": 4,
    "not_provided|Inborn_genetic_diseases|Anterior_segment_dysgenesis_7": 1,
    "not_specified|Anterior_segment_dysgenesis_7|not_provided": 3,
    "Anterior_segment_dysgenesis_7|not_provided|not_specified": 1,
    "Anterior_segment_dysgenesis_7|PXDN-related_disorder": 4,
    "PXDN-related_disorder|Anterior_segment_dysgenesis_7": 4,
    "PXDN-related_disorder|Anterior_segment_dysgenesis_7|not_provided": 2,
    "PXDN-related_disorder|Anterior_segment_dysgenesis_7|not_provided|Developmental_cataract": 1,
    "Anterior_segment_dysgenesis_7|PXDN-related_disorder|not_provided|not_specified": 1,
    "not_provided|Anterior_segment_dysgenesis_7|not_specified": 2,
    "PXDN-related_disorder|Anterior_segment_dysgenesis_7|not_provided|Inborn_genetic_diseases": 1,
    "Anterior_segment_dysgenesis": 7,
    "Glaucoma_3A": 17,
    "Inborn_genetic_diseases|Anterior_segment_dysgenesis_7|not_provided": 1,
    "PXDN-related_disorder|not_specified|not_provided|Anterior_segment_dysgenesis_7": 1,
    "Anterior_segment_dysgenesis_7|PXDN-related_disorder|not_provided": 1,
    "Anterior_segment_dysgenesis_7|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_39": 66,
    "MYT1L-related_disorder": 21,
    "Intellectual_disability|_autosomal_dominant_39|not_provided": 10,
    "not_provided|Intellectual_disability|_autosomal_dominant_39|not_specified": 1,
    "MYT1L-related_disorder|not_provided": 9,
    "not_provided|MYT1L-related_disorder": 7,
    "not_provided|Intellectual_disability|_autosomal_dominant_39": 8,
    "not_provided|Inborn_genetic_diseases|MYT1L-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_39|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_39|not_provided": 2,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_39|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_39": 1,
    "Neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_39": 1,
    "Intellectual_disability|_autosomal_dominant_39|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_39|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_39": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_39": 1,
    "not_provided|not_specified|MYT1L-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_39|not_provided": 1,
    "MYT1L-related_disorder|Intellectual_disability|_autosomal_dominant_39": 1,
    "Neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_39|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_39|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_39|MYT1L-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "MYT1L-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_39|not_specified": 1,
    "Neurodevelopmental_delay_with_neutropenia": 1,
    "Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome": 25,
    "not_provided|TRAPPC12-related_disorder|Inborn_genetic_diseases": 1,
    "TRAPPC12-related_disorder": 9,
    "TRAPPC12-related_disorder|not_provided": 7,
    "not_provided|Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome": 4,
    "Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome|Progressive_childhood_encephalopathy|TRAPPC12-related_disorder": 1,
    "Inborn_genetic_diseases|TRAPPC12-related_disorder|Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome|not_provided": 1,
    "Severe_hydrocephalus": 1,
    "not_provided|TRAPPC12-related_disorder|Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome": 3,
    "TRAPPC12-related_disorder|Inborn_genetic_diseases": 1,
    "Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome|not_provided": 2,
    "Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome|TRAPPC12-related_disorder|not_provided": 1,
    "not_provided|TRAPPC12-related_disorder": 6,
    "TRAPPC12-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|TRAPPC12-related_disorder": 1,
    "Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome|not_provided|TRAPPC12-related_disorder": 1,
    "Progressive_childhood_encephalopathy|Inborn_genetic_diseases|Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome": 1,
    "not_provided|RNASEH1-related_disorder": 9,
    "RNASEH1-related_disorder|not_provided": 6,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_2": 4,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_2|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_2": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_2": 1,
    "Diamond-Blackfan_anemia_8": 154,
    "not_provided|not_specified|Diamond-Blackfan_anemia_8": 1,
    "not_provided|Diamond-Blackfan_anemia_8": 2,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_8": 3,
    "Diamond-Blackfan_anemia_8|Diamond-Blackfan_anemia": 6,
    "Diamond-Blackfan_anemia_8|Diamond-Blackfan_anemia|not_provided": 1,
    "RPS7-related_disorder": 4,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_8|RPS7-related_disorder": 1,
    "Diamond-Blackfan_anemia_8|not_specified": 1,
    "Diamond-Blackfan_anemia_8|RPS7-related_disorder": 3,
    "not_specified|Diamond-Blackfan_anemia|not_provided|Diamond-Blackfan_anemia_8": 1,
    "not_specified|Diamond-Blackfan_anemia_8": 2,
    "not_specified|Diamond-Blackfan_anemia_8|not_provided": 1,
    "not_specified|Diamond-Blackfan_anemia_8|Diamond-Blackfan_anemia": 1,
    "COLEC11-related_disorder": 18,
    "3MC_syndrome_2": 10,
    "3MC_syndrome": 1,
    "COLEC11-related_disorder|not_provided": 3,
    "3MC_syndrome_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|3MC_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|COLEC11-related_disorder|not_provided": 1,
    "not_provided|3MC_syndrome_2": 1,
    "3MC_syndrome_2|not_provided": 1,
    "not_provided|COLEC11-related_disorder": 1,
    "Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism": 90,
    "not_provided|SOX11-related_disorder": 4,
    "Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism|not_provided": 10,
    "SOX11-related_disorder": 8,
    "not_provided|Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism": 6,
    "SOX11-related_disorder|Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism": 1,
    "SOX11-related_disorder|not_provided": 7,
    "not_provided|Coffin-Siris_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism": 2,
    "not_provided|Hypogonadotropic_hypogonadism": 4,
    "Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism|Inborn_genetic_diseases|not_provided": 1,
    "SLC35A2-congenital_disorder_of_glycosylation": 208,
    "not_provided|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism": 1,
    "Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism|Inborn_genetic_diseases": 2,
    "not_provided|Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism|Inborn_genetic_diseases": 2,
    "SOX11-related_disorder|Hypogonadotropic_hypogonadism|not_provided": 1,
    "Hypogonadotropic_hypogonadism|not_provided|SOX11-related_disorder": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SOX11-related_disorder": 1,
    "not_specified|SOX11-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_with_microcephaly_and_with_or_without_ocular_malformations_or_hypogonadotropic_hypogonadism|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism": 1,
    "Hypogonadotropic_hypogonadism|not_provided": 3,
    "not_specified|not_provided|SOX11-related_disorder": 1,
    "Inborn_genetic_diseases|SOX11-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism": 1,
    "Basal_ganglia_calcification|_idiopathic|_10|_autosomal_recessive": 3,
    "CMPK2-related_disorder": 4,
    "KIDINS220-related_disorder": 184,
    "not_provided|KIDINS220-related_disorder": 65,
    "Inborn_genetic_diseases|KIDINS220-related_disorder": 7,
    "KIDINS220-related_disorder|not_provided": 88,
    "not_specified|KIDINS220-related_disorder|not_provided": 1,
    "KIDINS220-related_disorder|not_provided|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|KIDINS220-related_disorder|not_provided": 6,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 31,
    "KIDINS220-related_disorder|Inborn_genetic_diseases": 7,
    "not_provided|Inborn_genetic_diseases|KIDINS220-related_disorder": 3,
    "not_provided|KIDINS220-related_disorder|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 1,
    "KIDINS220-related_disorder|Inborn_genetic_diseases|not_provided": 16,
    "Inborn_genetic_diseases|not_provided|KIDINS220-related_disorder": 6,
    "Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|KIDINS220-related_disorder|Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 1,
    "not_provided|KIDINS220-related_disorder|Inborn_genetic_diseases": 12,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided": 3,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis|KIDINS220-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 3,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided|Kabuki_syndrome_1": 1,
    "KCNA1-related_disorder": 4,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 1,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis|KIDINS220-related_disorder|not_provided": 1,
    "Ventriculomegaly_and_arthrogryposis": 5,
    "Ventriculomegaly_and_arthrogryposis|KIDINS220-related_disorder|not_provided": 1,
    "not_provided|Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 2,
    "not_specified|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis|not_provided": 1,
    "KIDINS220-related_disorder|not_specified|not_provided": 3,
    "not_provided|KIDINS220-related_disorder|Ventriculomegaly_and_arthrogryposis": 1,
    "Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis|not_provided": 2,
    "KIDINS220-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|KIDINS220-related_disorder": 1,
    "KIDINS220-related_disorder|Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided": 1,
    "not_provided|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis|Inborn_genetic_diseases|not_specified|KIDINS220-related_disorder": 1,
    "not_specified|not_provided|Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 1,
    "not_specified|not_provided|KIDINS220-related_disorder": 1,
    "KIDINS220-related_disorder|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 3,
    "not_provided|Ventriculomegaly_and_arthrogryposis": 1,
    "not_specified|KIDINS220-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Ventriculomegaly_and_arthrogryposis|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 2,
    "not_provided|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Inborn_genetic_diseases": 1,
    "KIDINS220-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided": 1,
    "not_provided|KIDINS220-related_disorder|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Inborn_genetic_diseases": 1,
    "KIDINS220-related_disorder|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|KIDINS220-related_disorder|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis": 1,
    "KIDINS220-related_disorder|not_provided|Inborn_genetic_diseases|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|Ventriculomegaly_and_arthrogryposis": 1,
    "KIDINS220-related_disorder|not_provided|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 1,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|KIDINS220-related_disorder|not_provided": 1,
    "Ventriculomegaly_and_arthrogryposis|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_nystagmus|_and_seizures": 4,
    "HP:0001252%3B_HP:0001776%3B_HP:0000252%3B_HP:0001270%3B_HP:0000592": 1,
    "not_specified|Neurodevelopmental_disorder_with_hypotonia|_microcephaly|_and_seizures": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_nystagmus|_and_seizures|not_specified": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_microcephaly|_and_seizures": 16,
    "not_specified|not_provided|Inflammatory_skin_and_bowel_disease|_neonatal|_1": 6,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_1": 408,
    "Inborn_genetic_diseases|Inflammatory_skin_and_bowel_disease|_neonatal|_1": 19,
    "Inborn_genetic_diseases|Inflammatory_skin_and_bowel_disease|_neonatal|_1|not_provided": 2,
    "ADAM17-related_disorder|Inflammatory_skin_and_bowel_disease|_neonatal|_1": 5,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_1|not_provided": 13,
    "not_provided|Inflammatory_skin_and_bowel_disease|_neonatal|_1": 7,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_1|Inborn_genetic_diseases": 11,
    "not_provided|not_specified|Inflammatory_skin_and_bowel_disease|_neonatal|_1": 1,
    "ADAM17-related_disorder|Inflammatory_skin_and_bowel_disease|_neonatal|_1|not_provided": 1,
    "ADAM17-related_disorder": 2,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_1|Neonatal_inflammatory_skin_and_bowel_disease": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_1|ADAM17-related_disorder": 3,
    "not_specified|Inflammatory_skin_and_bowel_disease|_neonatal|_1|not_provided": 1,
    "not_provided|Inflammatory_skin_and_bowel_disease|_neonatal|_1|ADAM17-related_disorder": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_1|not_specified": 1,
    "not_provided|Mycobacterium_tuberculosis|_susceptibility_to": 2,
    "Mycobacterium_tuberculosis|_susceptibility_to": 7,
    "Orofacial_cleft_1": 9,
    "Maturity-onset_diabetes_of_the_young_type_7": 74,
    "Maturity-onset_diabetes_of_the_young_type_7|not_provided": 13,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young": 100,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperglycemia": 1,
    "not_provided|KLF11-related_disorder": 4,
    "not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_7": 2,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_7|Type_2_diabetes_mellitus": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_7": 9,
    "KLF11-related_disorder": 8,
    "Maturity-onset_diabetes_of_the_young_type_7|KLF11-related_disorder": 1,
    "not_provided|not_specified|Monogenic_diabetes": 5,
    "Maturity-onset_diabetes_of_the_young_type_7|not_specified|not_provided": 3,
    "not_provided|not_specified|Maturity-onset_diabetes_of_the_young_type_7": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_7|not_specified": 1,
    "KLF11-related_disorder|Monogenic_diabetes|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_7": 1,
    "Monogenic_diabetes|not_provided": 70,
    "KLF11-related_disorder|not_provided": 5,
    "Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_7|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_7|not_provided|not_specified": 1,
    "Monogenic_diabetes|not_specified|Maturity-onset_diabetes_of_the_young_type_7|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_7|not_specified": 5,
    "Maturity-onset_diabetes_of_the_young_type_7|Diabetes_mellitus|not_provided": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_7": 1,
    "KLF11-related_disorder|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_7": 1,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_7": 1,
    "Maturity_onset_diabetes_mellitus_in_young": 235,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided": 143,
    "Autosomal_recessive_polycystic_kidney_disease": 3342,
    "CYS1-related_condition": 1,
    "Vascular_endothelial_growth_factor_(VEGF)_inhibitor_response": 11,
    "Cataract_13_with_adult_I_phenotype": 22,
    "Neurodevelopmental_disorder_with_alopecia_and_brain_abnormalities": 12,
    "ODC1-related_disorder": 4,
    "Inborn_genetic_diseases|ODC1-related_disorder|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_alopecia_and_brain_abnormalities|Inborn_genetic_diseases": 1,
    "Ornithine_decarboxylase_1_polymorphism|not_provided": 1,
    "Distal_renal_tubular_acidosis": 5,
    "Dextrocardia": 5,
    "ROCK2-related_disorder": 18,
    "ROCK2-related_disorder|not_provided": 1,
    "LPIN1-related_disorder": 5,
    "not_specified|Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided": 3,
    "not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive|LPIN1-related_disorder": 5,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive": 136,
    "Hyperchloremia|not_specified|LPIN1-related_disorder|not_provided": 1,
    "not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 33,
    "Acute_Recurrent_Myoglobinuria": 7,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided": 45,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided|LPIN1-related_disorder": 4,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 6,
    "LPIN1-related_disorder|not_provided": 6,
    "not_provided|not_specified|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 1,
    "not_provided|Inborn_genetic_diseases|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 5,
    "Inborn_genetic_diseases|Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided": 6,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|Inborn_genetic_diseases": 5,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive|Inborn_genetic_diseases": 6,
    "not_specified|not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 2,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 5,
    "not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_specified": 1,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided|not_specified": 2,
    "LPIN1-related_disorder|not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 1,
    "Acute_Recurrent_Myoglobinuria|not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_specified": 1,
    "not_provided|LPIN1-related_disorder": 3,
    "See_cases|Myoglobinuria|_acute_recurrent|_autosomal_recessive|LPIN1-related_disorder": 1,
    "Myoglobinuria|_acute_recurrent|_autosomal_recessive|LPIN1-related_disorder": 1,
    "LPIN1-related_disorder|Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_provided": 1,
    "not_specified|not_provided|LPIN1-related_disorder|Myoglobinuria|_acute_recurrent|_autosomal_recessive": 1,
    "not_provided|Myoglobinuria|_acute_recurrent|_autosomal_recessive|not_specified|Inborn_genetic_diseases": 1,
    "NBAS-related_disorder": 17,
    "not_provided|NBAS-related_disorder": 20,
    "not_specified|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|not_provided": 1,
    "NBAS-related_disorder|not_provided": 32,
    "not_provided|Inborn_genetic_diseases|Optic_atrophy": 5,
    "Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|not_provided": 5,
    "Inborn_genetic_diseases|Infantile_liver_failure_syndrome_2|not_provided": 1,
    "not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 33,
    "Infantile_liver_failure_syndrome_2|not_provided|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 5,
    "Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 13,
    "Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided": 8,
    "not_provided|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 6,
    "not_provided|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2": 12,
    "Infantile_liver_failure_syndrome_2|not_provided": 6,
    "not_provided|NBAS-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|Inborn_genetic_diseases": 1,
    "Infantile_liver_failure_syndrome_2": 19,
    "Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided": 7,
    "Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2": 6,
    "not_provided|Inborn_genetic_diseases|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 1,
    "NBAS-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|See_cases|not_provided": 1,
    "not_provided|Infantile_liver_failure_syndrome_2|not_specified": 2,
    "not_specified|Infantile_liver_failure_syndrome_2": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided": 16,
    "Inborn_genetic_diseases|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided": 1,
    "not_provided|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 4,
    "Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 3,
    "NBAS-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "NBAS-related_disorder|Infantile_liver_failure_syndrome_2|not_provided": 2,
    "not_provided|not_specified|NBAS-related_disorder": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 79,
    "not_specified|Optic_atrophy|not_provided": 1,
    "NBAS-related_disorder|not_specified|not_provided": 1,
    "not_provided|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Infantile_liver_failure_syndrome_2|Inborn_genetic_diseases": 1,
    "Optic_atrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 1,
    "NBAS-related_disorder|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|not_specified|not_provided": 1,
    "Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|NBAS-related_disorder": 1,
    "Infantile_liver_failure": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_liver_failure_syndrome_2": 1,
    "not_specified|not_provided|NBAS-related_disorder": 2,
    "Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_specified|not_provided": 2,
    "not_provided|Infantile_liver_failure_syndrome_2": 2,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided|Infantile_liver_failure": 1,
    "Optic_atrophy|not_provided": 39,
    "not_provided|NBAS-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Infantile_liver_failure_syndrome_2|not_provided": 2,
    "not_provided|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|not_provided": 2,
    "Infantile_liver_failure_syndrome_2|not_specified|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided": 5,
    "NBAS-related_disorder|not_provided|not_specified": 1,
    "Infantile_liver_failure|not_provided": 1,
    "not_specified|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided|Infantile_liver_failure_syndrome_2": 1,
    "NBAS-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|NBAS-related_disorder": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided": 1,
    "Retinal_dystrophy|not_provided|Infantile_liver_failure_syndrome_2|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|Infantile_liver_failure_syndrome_2|not_specified|not_provided": 3,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome": 1,
    "Infantile_liver_failure_syndrome_2|NBAS-related_disorder|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "not_provided|Neurodevelopmental_disorder|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_specified": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided|Infantile_liver_failure_syndrome_2": 1,
    "NBAS-related_disorder|Infantile_liver_failure_syndrome_2|Short_stature-optic_atrophy-Pelger-Hu\u00ebt_anomaly_syndrome|not_provided": 1,
    "MYCN-related_disorder": 18,
    "Feingold_syndrome_type_1": 35,
    "not_provided|MYCN-related_disorder|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome": 1,
    "Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome": 41,
    "MYCN-related_disorder|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome": 1,
    "not_provided|Feingold_syndrome_type_1": 6,
    "MYCN-related_disorder|not_provided": 4,
    "MYCN-related_disorder|not_provided|not_specified|Feingold_syndrome_type_1": 1,
    "Feingold_syndrome_type_1|not_provided": 8,
    "Inborn_genetic_diseases|Feingold_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome|not_provided": 2,
    "Megalencephaly-polydactyly_syndrome": 1,
    "MYCN-related_disorder|Megalencephaly-polydactyly_syndrome|not_provided": 1,
    "Megalencephaly-polydactyly_syndrome|See_cases": 1,
    "Inborn_genetic_diseases|Megalencephaly-polydactyly_syndrome|Feingold_syndrome_type_1": 2,
    "Inborn_genetic_diseases|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome": 2,
    "not_specified|not_provided|Feingold_syndrome_type_1|MYCN-related_disorder": 1,
    "Megalencephaly-polydactyly_syndrome|Feingold_syndrome_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome": 4,
    "not_provided|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome|MYCN-related_disorder|Inborn_genetic_diseases": 1,
    "Megalencephaly-polydactyly_syndrome|Feingold_syndrome_type_1|not_provided": 1,
    "Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome|not_provided": 2,
    "Feingold_syndrome_type_1|Megalencephaly-polydactyly_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Feingold_syndrome_type_1|MYCN-related_disorder": 2,
    "MYCN-related_disorder|not_specified|not_provided": 1,
    "not_provided|Feingold_syndrome_type_1|Feingold_syndrome": 1,
    "Feingold_syndrome|Feingold_syndrome_type_1": 1,
    "not_provided|Isolated_agenesis_of_gallbladder|Double_outlet_right_ventricle|Ventricular_septal_defect|Bilateral_cleft_palate": 1,
    "Spermatogenic_failure_88": 6,
    "Laterality_defects|_autosomal_dominant": 7,
    "GEN1-related_prostate_cancer|not_provided": 1,
    "GEN1-related_disorder": 2,
    "not_provided|not_specified|GEN1-related_prostate_cancer": 1,
    "not_provided|GEN1-related_disorder": 1,
    "GEN1-related_disorder|not_provided": 5,
    "not_provided|Olaparib_response": 3,
    "not_specified|not_provided|GEN1-related_disorder": 2,
    "Olaparib_response": 4,
    "GEN1-related_disorder|Breast_neoplasm|not_provided": 1,
    "KCNS3-related_disorder": 1,
    "Intellectual_disability|Cerebellar_atrophy": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 295,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 138,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided": 23,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided|Cranioectodermal_dysplasia_2": 2,
    "not_provided|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 8,
    "Short_rib-polydactyly_syndrome|Cranioectodermal_dysplasia": 5,
    "not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 8,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 12,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 9,
    "Cranioectodermal_dysplasia_2": 11,
    "Ellis-van_Creveld_syndrome|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|WDR35-related_disorder": 1,
    "WDR35-related_disorder|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 9,
    "WDR35-related_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Connective_tissue_disorder|WDR35-related_disorder|Cranioectodermal_dysplasia_2|not_provided": 1,
    "WDR35-related_disorder|not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 1,
    "WDR35-related_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 4,
    "not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided": 10,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_specified|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Inborn_genetic_diseases": 14,
    "not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_specified|not_provided": 1,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_specified|not_provided": 3,
    "WDR35-related_disorder": 8,
    "not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_specified": 1,
    "Connective_tissue_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_specified|not_provided|WDR35-related_disorder|Cranioectodermal_dysplasia_2": 1,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided|Inborn_genetic_diseases": 2,
    "Cranioectodermal_dysplasia_2|not_specified|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided": 1,
    "Cranioectodermal_dysplasia_2|WDR35-related_disorder": 1,
    "not_provided|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|WDR35-related_disorder": 1,
    "not_specified|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|WDR35-related_disorder|not_provided": 3,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder": 3,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder|Cranioectodermal_dysplasia_2|Inborn_genetic_diseases|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_specified|Cranioectodermal_dysplasia_2|not_provided": 2,
    "Cranioectodermal_dysplasia_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder": 1,
    "not_provided|Jeune_thoracic_dystrophy": 34,
    "Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 2,
    "not_provided|Inborn_genetic_diseases|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 2,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 3,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder|Cranioectodermal_dysplasia_2|not_provided": 2,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "WDR35-related_disorder|not_specified|not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_specified|WDR35-related_disorder|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Inborn_genetic_diseases|Cranioectodermal_dysplasia_2|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_2|WDR35-related_disorder|Cranioectodermal_dysplasia|Jeune_thoracic_dystrophy|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided": 1,
    "WDR35-related_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_specified": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Inborn_genetic_diseases|Cranioectodermal_dysplasia_2": 1,
    "Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Short_rib-polydactyly_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 4,
    "Short_rib-polydactyly_syndrome|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly": 2,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided": 2,
    "WDR35-related_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided": 1,
    "SHORT-RIB_THORACIC_DYSPLASIA_7_WITHOUT_POLYDACTYLY|Short_rib-polydactyly_syndrome|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_specified|not_provided": 1,
    "not_specified|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_provided": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_specified|WDR35-related_disorder|not_provided": 1,
    "not_provided|WDR35-related_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 1,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Connective_tissue_disorder|not_provided": 2,
    "WDR35-related_disorder|Cranioectodermal_dysplasia_2|Connective_tissue_disorder|not_specified|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder|Cranioectodermal_dysplasia_2": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Short_rib-polydactyly_syndrome|not_provided|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7/20_with_polydactyly|_digenic|SHORT-RIB_THORACIC_DYSPLASIA_7_WITHOUT_POLYDACTYLY|Jeune_thoracic_dystrophy": 1,
    "Connective_tissue_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|not_specified|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Connective_tissue_disorder|Cranioectodermal_dysplasia_2|not_provided": 1,
    "not_provided|Connective_tissue_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Cranioectodermal_dysplasia_2": 1,
    "Connective_tissue_disorder|Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_2|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|WDR35-related_disorder|not_provided|not_specified": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Cranioectodermal_dysplasia_2|WDR35-related_disorder|Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_7_with_or_without_polydactyly|Short_rib-polydactyly_syndrome|Multiple_Epiphyseal_Dysplasia|_Dominant|Cranioectodermal_dysplasia_2|not_specified|Cranioectodermal_dysplasia|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_5": 33,
    "Multiple_epiphyseal_dysplasia_type_5|Short_rib-polydactyly_syndrome|Cranioectodermal_dysplasia|Multiple_Epiphyseal_Dysplasia|_Dominant|not_provided": 1,
    "Multiple_Epiphyseal_Dysplasia|_Dominant|Cranioectodermal_dysplasia|not_provided|Short_rib-polydactyly_syndrome|Multiple_epiphyseal_dysplasia_type_5|not_specified": 1,
    "Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia_type_5|Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Osteoarthritis_susceptibility_2|not_provided": 1,
    "MATN3-related_disorder|not_provided": 1,
    "not_specified|not_provided|Multiple_epiphyseal_dysplasia_type_5": 2,
    "Multiple_epiphyseal_dysplasia_type_5|not_provided|Connective_tissue_disorder|not_specified": 1,
    "not_provided|MATN3-related_disorder": 3,
    "not_provided|Multiple_epiphyseal_dysplasia_type_5": 10,
    "Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Multiple_epiphyseal_dysplasia_type_5|Osteoarthritis_susceptibility_2": 4,
    "MATN3-related_disorder": 2,
    "Multiple_epiphyseal_dysplasia_type_5|Connective_tissue_disorder|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_matrilin-3_type": 1,
    "not_specified|Multiple_epiphyseal_dysplasia_type_5|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_5|MATN3-related_disorder|Osteoarthritis_susceptibility_2|not_provided|not_specified|Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Connective_tissue_disorder": 1,
    "not_provided|Osteoarthritis_susceptibility_2": 1,
    "not_specified|not_provided|Multiple_epiphyseal_dysplasia_type_5|Connective_tissue_disorder": 1,
    "Multiple_epiphyseal_dysplasia_type_5|Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Osteoarthritis_susceptibility_2|not_provided": 1,
    "Multiple_epiphyseal_dysplasia|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Connective_tissue_disorder|Multiple_epiphyseal_dysplasia_type_5|not_provided": 2,
    "Multiple_epiphyseal_dysplasia_type_5|not_specified": 1,
    "Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Multiple_epiphyseal_dysplasia|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Multiple_epiphyseal_dysplasia_type_5|Multiple_epiphyseal_dysplasia|not_provided": 2,
    "Multiple_epiphyseal_dysplasia": 9,
    "not_provided|Multiple_epiphyseal_dysplasia": 3,
    "not_provided|not_specified|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Multiple_epiphyseal_dysplasia_type_5|Multiple_epiphyseal_dysplasia": 1,
    "Connective_tissue_disorder|Multiple_epiphyseal_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_5|Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|not_provided|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Multiple_epiphyseal_dysplasia|Inborn_genetic_diseases|not_provided|Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Multiple_epiphyseal_dysplasia|not_provided|Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 30,
    "not_provided|Multiple_epiphyseal_dysplasia_type_5|Inborn_genetic_diseases": 2,
    "Connective_tissue_disorder|not_provided|Multiple_epiphyseal_dysplasia_type_5|MATN3-related_disorder": 1,
    "Multiple_epiphyseal_dysplasia_type_5|not_provided": 3,
    "not_provided|Multiple_epiphyseal_dysplasia_type_5|Connective_tissue_disorder|not_specified": 1,
    "Osteoarthritis_susceptibility_2": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Multiple_epiphyseal_dysplasia_type_5": 1,
    "Spondyloepimetaphyseal_dysplasia|_matrilin-3_type|Osteoarthritis_susceptibility_2|Multiple_epiphyseal_dysplasia_type_5": 1,
    "not_provided|Multiple_Epiphyseal_Dysplasia|_Dominant": 2,
    "RHOB-related_disorder|\"See_Cases\"|not_specified|Recurrent_pancreatitis": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 993,
    "Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 15,
    "Familial_hypobetalipoproteinemia_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 301,
    "Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 14,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 18,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 2,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 5,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia": 8,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype": 64,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 358,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia": 1,
    "not_provided|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B": 36,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|not_provided": 16,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 93,
    "Cardiovascular_phenotype|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 5,
    "not_specified|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 4,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1": 2,
    "APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 41,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 13,
    "Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 36,
    "APOB-related_disorder": 9,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified": 1,
    "Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 2,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 39,
    "Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Cardiovascular_phenotype": 3,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype": 134,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1": 5,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|not_provided": 2,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 44,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided|APOB-related_disorder": 1,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 3,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|not_specified": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia": 19,
    "Hypobetalipoproteinemia": 4,
    "not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 9,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Warfarin_response": 3,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype": 18,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 30,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 41,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "APOB-related_disorder|Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 2,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype": 4,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 9,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 8,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 6,
    "not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 24,
    "Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 3,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided": 22,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder": 2,
    "Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype": 10,
    "Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_specified": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia": 11,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 26,
    "Hypercholesterolemia|_familial|_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 2,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 4,
    "APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 6,
    "Cardiovascular_phenotype|not_specified|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 16,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|APOB-related_disorder|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|not_provided": 4,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 16,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Cardiovascular_phenotype": 10,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 20,
    "not_provided|APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 4,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 2,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|not_specified|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 5,
    "not_provided|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1": 2,
    "not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 4,
    "Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype": 2,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 3,
    "APOB-related_disorder|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hypercholesterolemia": 3,
    "Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 7,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 7,
    "Cardiovascular_phenotype|APOB-related_disorder|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 2,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|not_specified": 1,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype": 2,
    "not_provided|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 2,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 3,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|not_provided|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|not_provided": 3,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified": 1,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 5,
    "APOB-related_disorder|Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypobetalipoproteinemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|APOB-related_disorder|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_autosomal_dominant|_3|Cardiovascular_phenotype": 1,
    "Familial_hypobetalipoproteinemia_1|APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypobetalipoproteinemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Familial_hypercholesterolemia|not_provided|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 2,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 5,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1": 4,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 3,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1|APOB-related_disorder": 1,
    "not_specified|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 5,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "not_provided|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|APOB-related_disorder": 1,
    "Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|not_specified|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1": 2,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypercholesterolemia": 5,
    "Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Familial_hypercholesterolemia|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 2,
    "Familial_hypobetalipoproteinemia|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Early-onset_coronary_artery_disease|not_provided": 1,
    "not_provided|Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 2,
    "Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|APOB-related_disorder|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|not_specified": 2,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder": 3,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypobetalipoproteinemia": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|APOB-related_disorder": 2,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "APOB-related_disorder|Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 2,
    "Cardiovascular_phenotype|Neutrophilia_in_presence_of_infection|Isolated_systolic_hypertension|Triangular_shaped_proximal_phalanx_of_the_thumb|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 2,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "Familial_hypobetalipoproteinemia_1": 15,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Hypobetalipoproteinemia|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Familial_hypobetalipoproteinemia": 2,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|not_provided": 1,
    "not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 2,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 4,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 3,
    "APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Familial_hypercholesterolemia|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified": 2,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1": 2,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided|Familial_hypobetalipoproteinemia": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 4,
    "APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_specified": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|APOB-related_disorder": 2,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 3,
    "Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_provided": 1,
    "Familial_hypercholesterolemia|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|APOB-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder|Familial_hypercholesterolemia|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|Cardiovascular_phenotype": 2,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|APOB-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 1,
    "not_provided|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_specified": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided": 3,
    "not_provided|Familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 2,
    "not_provided|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 2,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 3,
    "Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 1,
    "not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|Familial_hypercholesterolemia": 1,
    "APOB-related_disorder|not_specified|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 2,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Familial_hypobetalipoproteinemia|not_provided|APOB-related_disorder": 1,
    "Hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 4,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|not_provided|Hypercholesterolemia|_familial|_1|not_specified|Familial_hypobetalipoproteinemia_1": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|APOB-related_disorder": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|not_specified": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|APOB-related_disorder": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|not_provided": 1,
    "not_specified|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 1,
    "Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|APOB-related_disorder": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified": 1,
    "Cardiovascular_phenotype|Spastic_ataxia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 4,
    "APOB-related_disorder|Cardiovascular_phenotype|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided": 1,
    "not_specified|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Cardiovascular_phenotype|APOB-related_disorder": 1,
    "Hypobetalipoproteinemia|Familial_hypobetalipoproteinemia_1": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|APOB-related_disorder": 1,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Familial_hypercholesterolemia|not_specified|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Familial_hypobetalipoproteinemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Familial_hypercholesterolemia|APOB-related_disorder|Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Early-onset_coronary_artery_disease": 2,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "APOB-related_disorder|not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|APOB-related_disorder|not_specified": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Familial_hypobetalipoproteinemia_1": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1|Warfarin_response": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia|not_specified|not_provided": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|not_specified": 2,
    "APOB-related_disorder|Cardiovascular_phenotype|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Familial_hypobetalipoproteinemia_1|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|not_provided|not_specified|APOB-related_disorder|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|not_specified|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_familial|_1|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "APOB-related_disorder|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_provided": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_specified": 1,
    "Familial_hypobetalipoproteinemia_1|Hypobetalipoproteinemia": 1,
    "not_provided|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_provided|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "APOB-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|not_provided|APOB-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1|Warfarin_response": 1,
    "not_provided|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|APOB-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|Familial_hypobetalipoproteinemia_1|Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B": 1,
    "Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Hypobetalipoproteinemia": 1,
    "Cardiovascular_phenotype|APOB-related_disorder|Familial_hypobetalipoproteinemia_1|Hypercholesterolemia|_autosomal_dominant|_type_B|not_specified|Familial_hypercholesterolemia|not_provided": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_autosomal_dominant|_type_B|Familial_hypobetalipoproteinemia_1|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|not_provided|APOB_POLYMORPHISM_IN_SIGNAL_PEPTIDE": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_autosomal_dominant|_type_B|Hypercholesterolemia|_familial|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1654,
    "TP53I3-related_disorder": 20,
    "not_specified|TP53I3-related_disorder": 2,
    "TP53I3-related_disorder|not_specified": 1,
    "Essential_tremor": 10,
    "ITSN2-related_disorder": 41,
    "not_provided|ITSN2-related_disorder": 17,
    "ITSN2-related_disorder|not_specified": 2,
    "Landau-Kleffner_syndrome": 1319,
    "not_specified|ITSN2-related_disorder": 1,
    "ITSN2-related_disorder|not_provided": 13,
    "not_provided|not_specified|ITSN2-related_disorder": 1,
    "not_specified|ITSN2-related_disorder|not_provided": 1,
    "ITSN2-related_disorder|not_specified|not_provided": 2,
    "NCOA1-related_disorder": 256,
    "NCOA1-related_disorder|not_specified": 19,
    "not_specified|NCOA1-related_disorder": 29,
    "NCOA1-related_disorder|not_provided": 3,
    "not_provided|NCOA1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_early-onset_parkinsonism_and_behavioral_abnormalities": 3,
    "not_provided|not_specified|PTRHD1-related_disorder": 1,
    "PTRHD1-related_disorder": 5,
    "Neurodevelopmental_disorder_with_early-onset_parkinsonism_and_behavioral_abnormalities|not_provided": 1,
    "Parkinsonian_disorder|Neurodevelopmental_disorder_with_early-onset_parkinsonism_and_behavioral_abnormalities": 1,
    "ADCY3-related_disorder": 295,
    "ADCY3-related_disorder|Inborn_genetic_diseases": 19,
    "ADCY3-related_disorder|not_provided": 21,
    "ADCY3-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_19": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_19": 6,
    "not_provided|ADCY3-related_disorder": 20,
    "Inborn_genetic_diseases|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_19": 1,
    "Inborn_genetic_diseases|ADCY3-related_disorder": 13,
    "Inborn_genetic_diseases|ADCY3-related_disorder|not_provided": 1,
    "ADCY3-related_disorder|not_specified|not_provided": 1,
    "not_provided|ADCY3-related_disorder|Inborn_genetic_diseases": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|Obesity": 8,
    "not_provided|Obesity_due_to_pro-opiomelanocortin_deficiency|Obesity": 3,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|Monogenic_Non-Syndromic_Obesity": 1,
    "POMC-related_disorder": 72,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|POMC-related_disorder|Obesity": 1,
    "not_provided|POMC-related_disorder": 9,
    "Inborn_genetic_diseases|POMC-related_disorder|not_provided": 2,
    "POMC-related_disorder|not_provided": 12,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|Inherited_obesity|Obesity|_early-onset|_susceptibility_to|POMC-related_disorder|not_provided": 1,
    "not_provided|Obesity_due_to_pro-opiomelanocortin_deficiency|POMC-related_disorder|Obesity": 1,
    "POMC-related_disorder|not_specified|not_provided|Obesity": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|POMC-related_disorder|not_provided|Obesity": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|not_provided": 2,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|Inherited_obesity|not_specified|POMC-related_disorder|not_provided": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|not_provided|POMC-related_disorder|Obesity": 1,
    "Inborn_genetic_diseases|POMC-related_disorder": 2,
    "Obesity|Obesity_due_to_pro-opiomelanocortin_deficiency|not_provided|POMC-related_disorder": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency": 9,
    "POMC-related_disorder|Obesity_due_to_pro-opiomelanocortin_deficiency|Obesity|not_provided": 1,
    "POMC-related_disorder|not_provided|Obesity_due_to_pro-opiomelanocortin_deficiency|Obesity": 2,
    "POMC-related_disorder|not_provided|Obesity_due_to_pro-opiomelanocortin_deficiency|not_specified|Obesity": 1,
    "POMC-related_disorder|Obesity|not_specified|not_provided": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|not_specified|not_provided|Monogenic_Non-Syndromic_Obesity": 1,
    "Inherited_obesity|not_provided|Obesity_due_to_pro-opiomelanocortin_deficiency": 1,
    "POMC-related_disorder|not_specified": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|POMC-related_disorder|Inborn_genetic_diseases|Obesity": 1,
    "Obesity|Obesity_due_to_pro-opiomelanocortin_deficiency|not_provided|not_specified": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|Inherited_obesity|POMC-related_disorder|not_provided|Obesity": 1,
    "POMC-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|POMC-related_disorder|Inherited_obesity": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|POMC-related_disorder": 1,
    "not_provided|Obesity|not_specified|Obesity_due_to_pro-opiomelanocortin_deficiency": 1,
    "POMC-related_disorder|Obesity_due_to_pro-opiomelanocortin_deficiency|Obesity": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|not_provided|Obesity": 1,
    "Obesity_due_to_pro-opiomelanocortin_deficiency|Inherited_obesity": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome": 317,
    "Heyn-Sproul-Jackson_syndrome": 6,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases": 25,
    "not_provided|Tatton-Brown-Rahman_overgrowth_syndrome": 15,
    "DNMT3A-related_disorder|not_provided": 4,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome|Autism_spectrum_disorder|not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "DNMT3A-related_disorder|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder|Inborn_genetic_diseases": 7,
    "DNMT3A-related_disorder|not_provided|Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Acute_myeloid_leukemia": 589,
    "Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome": 24,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Abnormality_of_the_nervous_system|Intellectual_disability|EBV-positive_nodal_T-_and_NK-cell_lymphoma|DNMT3A-related_disorder|Clonal_Cytopenia_of_Undetermined_Significance|Inborn_genetic_diseases|not_specified|not_provided|Acute_myeloid_leukemia": 1,
    "not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|EBV-positive_nodal_T-_and_NK-cell_lymphoma|DNMT3A-related_disorder|Neurodevelopmental_disorder|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 16,
    "Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder": 4,
    "DNMT3A-related_disorder": 98,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome": 2,
    "not_specified|DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome": 29,
    "Acute_myeloid_leukemia|Tatton-Brown-Rahman_overgrowth_syndrome": 2,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder": 12,
    "Inborn_genetic_diseases|DNMT3A-related_disorder": 10,
    "Heyn-Sproul-Jackson_syndrome|Acute_myeloid_leukemia|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Acute_myeloid_leukemia|Inborn_genetic_diseases|not_provided": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Melanoma": 1,
    "DNMT3A-related_disorder|Inborn_genetic_diseases": 4,
    "Intellectual_disability|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Malignant_lymphoma|_large_B-cell|_diffuse|Myeloproliferative_disorder|not_specified|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder": 1,
    "Inborn_genetic_diseases|DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome": 7,
    "Inborn_genetic_diseases|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|not_specified|DNMT3A-related_disorder": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder|Heyn-Sproul-Jackson_syndrome": 1,
    "DNMT3A-related_disorder|Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome": 4,
    "Autism_spectrum_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|Heyn-Sproul-Jackson_syndrome|Acute_myeloid_leukemia|not_provided": 1,
    "not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|DNMT3A-related_disorder": 2,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Acute_myeloid_leukemia|DNMT3A-related_disorder": 1,
    "Acute_myeloid_leukemia|Heyn-Sproul-Jackson_syndrome|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "DNMT3A-related_disorder|Autism_spectrum_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia|Heyn-Sproul-Jackson_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 2,
    "Tatton-Brown-Rahman_overgrowth_syndrome|not_provided|See_cases": 1,
    "DNMT3A-related_disorder|Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 3,
    "not_provided|DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome": 3,
    "DNMT3A-related_disorder|Inborn_genetic_diseases|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Obesity|Macrocephaly|Optic_disc_pallor|Specific_learning_disability|Large_for_gestational_age|Global_developmental_delay|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "not_provided|DNMT3A-related_disorder|Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Hypoparathyroidism|See_cases": 1,
    "DNMT3A-related_disorder|Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome|not_specified|not_provided": 1,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|DNMT3A-related_disorder|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|DNMT3A-related_disorder": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|not_specified|DNMT3A-related_disorder": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|DNMT3A-related_disorder": 3,
    "Early_T_cell_progenitor_acute_lymphoblastic_leukemia": 2,
    "Inborn_genetic_diseases|not_provided|DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "DNMT3A-related_disorder|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder|not_provided|not_specified": 1,
    "not_specified|Tatton-Brown-Rahman_overgrowth_syndrome": 2,
    "Neonatal_hypotonia|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|Autism_spectrum_disorder": 1,
    "not_provided|Heyn-Sproul-Jackson_syndrome": 1,
    "Intellectual_disability|Tatton-Brown-Rahman_overgrowth_syndrome": 2,
    "not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Inborn_genetic_diseases|Heyn-Sproul-Jackson_syndrome|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 1,
    "not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|DNMT3A-related_disorder|not_provided": 1,
    "Heyn-Sproul-Jackson_syndrome|Acute_myeloid_leukemia|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 1,
    "not_provided|DNMT3A-related_disorder": 2,
    "DNMT3A-related_disorder|not_provided|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|not_provided|DNMT3A-related_disorder": 2,
    "not_specified|DNMT3A-related_disorder": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Acute_myeloid_leukemia|Heyn-Sproul-Jackson_syndrome|DNMT3A-related_disorder": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder|not_provided": 2,
    "not_provided|Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder": 2,
    "not_specified|DNMT3A-related_disorder|Inborn_genetic_diseases|Tatton-Brown-Rahman_overgrowth_syndrome": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Acute_myeloid_leukemia|Heyn-Sproul-Jackson_syndrome|not_provided|DNMT3A-related_disorder": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|not_specified": 1,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|not_specified|not_provided": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|DNMT3A-related_disorder|not_specified": 1,
    "DNMT3A-related_disorder|Tatton-Brown-Rahman_overgrowth_syndrome|not_specified": 1,
    "Tatton-Brown-Rahman_overgrowth_syndrome|Acute_myeloid_leukemia": 1,
    "Craniosynostosis_syndrome|Tatton-Brown-Rahman_overgrowth_syndrome|not_provided": 1,
    "ASXL2-related_disorder|not_provided": 9,
    "not_provided|ASXL2-related_disorder": 8,
    "Shashi-Pena_syndrome": 46,
    "not_provided|Shashi-Pena_syndrome": 4,
    "Syndromic_intellectual_disability|not_provided": 6,
    "Inborn_genetic_diseases|Shashi-Pena_syndrome": 3,
    "ASXL2-related_disorder": 9,
    "Inborn_genetic_diseases|Shashi-Pena_syndrome|not_provided": 1,
    "ASXL2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Shashi-Pena_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|ASXL2-related_disorder": 2,
    "Shashi-Pena_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|ASXL2-related_disorder": 1,
    "ASXL2-related_disorder|Vascular_disorder": 1,
    "ASXL2-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|ASXL2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Syndromic_intellectual_disability": 2,
    "Severe_hydrocephalus|Abnormal_cerebellum_morphology": 1,
    "Inborn_genetic_diseases|Developmental_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|ASXL2-related_disorder|Shashi-Pena_syndrome": 1,
    "Intellectual_disability|not_provided|Shashi-Pena_syndrome": 1,
    "KIF3C-related_neurodevelopmental_disorder": 1,
    "CIC-rearranged_sarcoma": 17,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 373,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided": 14,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 311,
    "not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 6,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 11,
    "HADHA-related_disorder|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency_1|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|HADHA-related_disorder": 1,
    "Mitochondrial_trifunctional_protein_deficiency|HADHA-related_disorder|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 8,
    "not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency": 385,
    "not_specified|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|HADHA-related_disorder": 1,
    "not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases|HADHA-related_disorder": 1,
    "Seckel_syndrome_6": 10,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|not_provided": 3,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|HADHA-related_disorder|not_provided": 1,
    "Mitochondrial_trifunctional_protein_deficiency_1|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided": 2,
    "HADHA-related_disorder|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 6,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 8,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_1": 2,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "HADHA-related_disorder|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency": 7,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 2,
    "not_provided|Inborn_genetic_diseases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 1,
    "See_cases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "Inborn_genetic_diseases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided": 2,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided|not_specified": 3,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|not_specified": 1,
    "not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 5,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_specified": 7,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "HADHA-related_disorder": 5,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_specified": 3,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency_1|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 2,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_specified|not_provided": 3,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|HADHA-related_disorder": 7,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 11,
    "Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 5,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided|HADHA-related_disorder": 2,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_1": 2,
    "Inborn_genetic_diseases|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|HADHA-related_disorder|Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases|Metabolic_disease|not_specified|not_provided|LCHAD_deficiency_with_maternal_acute_fatty_liver_of_pregnancy": 1,
    "HADHA-related_disorder|not_provided": 1,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency_1|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 2,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 7,
    "not_specified|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|HADHA-related_disorder": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|HADHA-related_disorder|not_specified": 1,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 2,
    "not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|HADHA-related_disorder|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases": 4,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|HADHA-related_disorder": 1,
    "HADHA-related_disorder|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|not_provided": 1,
    "Mitochondrial_trifunctional_protein_deficiency_1": 5,
    "not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases": 3,
    "Mitochondrial_trifunctional_protein_deficiency|not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "not_specified|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 2,
    "HADHA-related_disorder|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Mitochondrial_trifunctional_protein_deficiency_1|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "Mitochondrial_trifunctional_protein_deficiency_1|not_specified": 1,
    "HADHA-related_disorder|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 2,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency|HADHA-related_disorder": 1,
    "HADHA-related_disorder|not_provided|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "not_specified|Mitochondrial_trifunctional_protein_deficiency|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|HADHA-related_disorder|not_provided": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency|not_provided": 1,
    "not_provided|HADHA-related_disorder": 1,
    "HADHA-related_disorder|not_specified|not_provided|Long_chain_3-hydroxyacyl-CoA_dehydrogenase_deficiency|Mitochondrial_trifunctional_protein_deficiency": 1,
    "HADHB-related_disorder|Mitochondrial_trifunctional_protein_deficiency": 4,
    "HADHA-related_disorder|Mitochondrial_trifunctional_protein_deficiency": 2,
    "Mitochondrial_trifunctional_protein_deficiency|not_provided": 15,
    "not_specified|Mitochondrial_trifunctional_protein_deficiency|not_provided": 2,
    "HADHB-related_disorder|Mitochondrial_trifunctional_protein_deficiency|not_specified": 1,
    "Mitochondrial_trifunctional_protein_deficiency|not_specified": 4,
    "Mitochondrial_trifunctional_protein_deficiency_2": 11,
    "Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency_2": 1,
    "not_provided|HADHB-related_disorder": 1,
    "Metabolic_acidosis|Renal_tubular_acidosis|Rickets": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases": 5,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency": 9,
    "Mitochondrial_trifunctional_protein_deficiency_1|not_provided|Mitochondrial_trifunctional_protein_deficiency": 2,
    "Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency_2|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency|HADHB-related_disorder": 4,
    "not_specified|Mitochondrial_trifunctional_protein_deficiency": 5,
    "Mitochondrial_trifunctional_protein_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_1": 3,
    "Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency": 4,
    "HADHB-related_disorder|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_1": 3,
    "Mitochondrial_trifunctional_protein_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_2": 2,
    "Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency_1|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "HADHB-related_disorder": 3,
    "Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_2": 2,
    "Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency_2": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency": 2,
    "Mitochondrial_trifunctional_protein_deficiency_2|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency_2|Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "not_specified|not_provided|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency|HADHB-related_disorder|Inborn_genetic_diseases": 1,
    "Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency": 3,
    "not_specified|not_provided|Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "Mitochondrial_trifunctional_protein_deficiency_2|not_specified": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_1|HADHB-related_disorder": 1,
    "Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_1": 1,
    "not_specified|Mitochondrial_trifunctional_protein_deficiency_2|not_provided|Mitochondrial_trifunctional_protein_deficiency": 2,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency_2|not_specified|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency|not_specified|not_provided": 1,
    "Mitochondrial_trifunctional_protein_deficiency|not_provided|Mitochondrial_trifunctional_protein_deficiency_2|not_specified": 1,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency_2": 1,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency|HADHB-related_disorder": 1,
    "Mitochondrial_trifunctional_protein_deficiency_1|Mitochondrial_trifunctional_protein_deficiency": 1,
    "Mitochondrial_trifunctional_protein_deficiency|Mitochondrial_trifunctional_protein_deficiency_2_with_myopathy_and_neuropathy": 1,
    "not_provided|Mitochondrial_trifunctional_protein_deficiency_2|Mitochondrial_trifunctional_protein_deficiency": 2,
    "Mitochondrial_trifunctional_protein_deficiency_1|Inborn_genetic_diseases|Mitochondrial_trifunctional_protein_deficiency|not_provided": 1,
    "Spastic_paraplegia_81|_autosomal_recessive": 5,
    "SELENOI-related_condition": 1,
    "not_specified|Spastic_paraplegia_81|_autosomal_recessive": 2,
    "not_provided|Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 4,
    "not_provided|Primary_ciliary_dyskinesia_21|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Inborn_genetic_diseases": 53,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 47,
    "not_provided|Primary_ciliary_dyskinesia_21|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_21": 5,
    "Kartagener_syndrome": 35,
    "Primary_ciliary_dyskinesia|not_provided": 352,
    "Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia": 3,
    "Spermatogenic_failure_80|not_provided": 1,
    "DRC1-related_disorder|Primary_ciliary_dyskinesia": 3,
    "DRC1-related_disorder|Spermatogenic_failure_80|Primary_ciliary_dyskinesia_21|Primary_ciliary_dyskinesia|not_provided|not_specified": 1,
    "not_provided|Primary_ciliary_dyskinesia": 359,
    "Primary_ciliary_dyskinesia_21|Primary_ciliary_dyskinesia": 3,
    "Primary_ciliary_dyskinesia_21|not_specified|not_provided|Primary_ciliary_dyskinesia": 4,
    "Spermatogenic_failure_80": 5,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_21": 6,
    "Primary_ciliary_dyskinesia|DRC1-related_disorder": 4,
    "Primary_ciliary_dyskinesia_21|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_21|Primary_ciliary_dyskinesia": 1,
    "Spermatogenic_failure_80|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia|DRC1-related_disorder|Primary_ciliary_dyskinesia_21": 1,
    "Spermatogenic_failure_80|Primary_ciliary_dyskinesia_21|Primary_ciliary_dyskinesia|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia_21|Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 1,
    "DRC1-related_disorder|Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia_21|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|DRC1-related_disorder|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia|not_specified|not_provided": 29,
    "not_provided|Primary_ciliary_dyskinesia|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_21|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_21": 1,
    "Inborn_genetic_diseases|DRC1-related_disorder|Primary_ciliary_dyskinesia": 1,
    "DRC1-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia": 24,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9": 186,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 29,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 52,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified": 11,
    "Auditory_neuropathy|_autosomal_recessive|_1": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Rare_genetic_deafness": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|not_provided": 10,
    "OTOF-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "OTOF-related_disorder": 3,
    "not_provided|Auditory_neuropathy_spectrum_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Hearing_loss|_autosomal_recessive|Auditory_neuropathy_spectrum_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|not_specified": 22,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Auditory_neuropathy|_autosomal_recessive|_1": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 21,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|Bilateral_sensorineural_hearing_impairment": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|not_specified|Bilateral_sensorineural_hearing_impairment": 1,
    "not_provided|OTOF-related_disorder": 8,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Hearing_loss|_autosomal_recessive": 2,
    "Tricho-oculo-dermo-vertebral_syndrome": 2,
    "OTOF-related_disorder|not_provided": 4,
    "Nonsyndromic_genetic_hearing_loss|not_provided": 14,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "OTOF-related_disorder|not_provided|not_specified": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9": 3,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Auditory_neuropathy_spectrum_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|OTOF-related_disorder|not_specified": 4,
    "not_provided|Bilateral_sensorineural_hearing_impairment": 4,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 2,
    "not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|not_specified": 3,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Auditory_neuropathy|Autosomal_recessive_nonsyndromic_hearing_loss_9": 3,
    "Hearing_loss|_autosomal_recessive|Auditory_neuropathy_spectrum_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Auditory_neuropathy_spectrum_disorder|Rare_genetic_deafness|not_specified|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "OTOF-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Auditory_neuropathy": 1,
    "not_specified|not_provided|OTOF-related_disorder": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Auditory_neuropathy|_autosomal_recessive|_1": 2,
    "Hearing_loss|_autosomal_recessive|Bilateral_sensorineural_hearing_impairment": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|Rare_genetic_deafness": 1,
    "Tricho-oculo-dermo-vertebral_syndrome|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Nonsyndromic_genetic_hearing_loss": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Bilateral_sensorineural_hearing_impairment|not_provided": 2,
    "OTOF-related_disorder|Rare_genetic_deafness|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_9|Bilateral_sensorineural_hearing_impairment": 1,
    "not_provided|not_specified|Nonsyndromic_genetic_hearing_loss|OTOF-related_disorder": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_9|Rare_genetic_deafness": 1,
    "not_specified|Hearing_impairment|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|OTOF-related_disorder|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Nonsyndromic_genetic_hearing_loss": 48,
    "not_provided|Rare_genetic_deafness": 49,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|Inborn_genetic_diseases|OTOF-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Auditory_neuropathy_spectrum_disorder|OTOF-related_disorder|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|not_provided|OTOF-related_disorder": 1,
    "OTOF-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3": 438,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Auditory_neuropathy_spectrum_disorder|not_provided": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Bilateral_sensorineural_hearing_impairment|OTOF-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 1,
    "Monogenic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Bilateral_sensorineural_hearing_impairment": 1,
    "not_provided|Auditory_neuropathy": 5,
    "not_provided|Auditory_neuropathy_spectrum_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Bilateral_sensorineural_hearing_impairment": 4,
    "not_provided|not_specified|Bilateral_sensorineural_hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder|not_provided": 1,
    "Pendred_syndrome": 155,
    "Nonsyndromic_genetic_hearing_loss|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|OTOF-related_disorder|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Auditory_neuropathy_spectrum_disorder": 11,
    "not_provided|OTOF-related_disorder|Hearing_loss|_autosomal_recessive": 1,
    "OTOF-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 1,
    "Rare_genetic_deafness|OTOF-related_disorder|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Auditory_neuropathy_spectrum_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "not_provided|OTOF-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness|Bilateral_sensorineural_hearing_impairment|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Inborn_genetic_diseases": 2,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder": 1,
    "not_specified|OTOF-related_disorder|not_provided": 3,
    "not_provided|OTOF-related_disorder|not_specified": 2,
    "Rare_genetic_deafness|OTOF-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Bilateral_sensorineural_hearing_impairment": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_9|Rare_genetic_deafness|OTOF-related_disorder|Nonsyndromic_genetic_hearing_loss": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Hearing_impairment": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|Nonsyndromic_genetic_hearing_loss|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified": 3,
    "not_provided|Auditory_neuropathy|_autosomal_recessive|_1|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Hearing_impairment|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "not_specified|Nonsyndromic_genetic_hearing_loss|not_provided": 2,
    "Hearing_loss|_autosomal_recessive|Nonsyndromic_genetic_hearing_loss|Deafness": 1,
    "Rare_genetic_deafness|not_provided|Auditory_neuropathy|_autosomal_recessive|_1|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "not_specified|OTOF-related_disorder|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|OTOF-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 1,
    "Bilateral_sensorineural_hearing_impairment": 4,
    "not_provided|OTOF-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified": 1,
    "Auditory_neuropathy_spectrum_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "not_provided|not_specified|OTOF-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder": 1,
    "not_specified|not_provided|OTOF-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified|OTOF-related_disorder": 1,
    "OTOF-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided|not_specified|OTOF-related_disorder": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder": 1,
    "Hearing_loss|_autosomal_recessive|not_provided": 18,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9|OTOF-related_disorder|Childhood_onset_hearing_loss": 1,
    "not_provided|Auditory_neuropathy_spectrum_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_9|not_provided": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss": 8,
    "Autosomal_recessive_nonsyndromic_hearing_loss_9|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|OTOF-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "KCNK3-related_disorder": 2,
    "Pulmonary_hypertension|_primary|_4": 171,
    "Pulmonary_hypertension|_primary|_4|Inborn_genetic_diseases": 8,
    "KCNK3-related_disorder|Pulmonary_hypertension|_primary|_4": 1,
    "Pulmonary_hypertension|_primary|_4|KCNK3-related_disorder": 1,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_4": 5,
    "not_provided|Pulmonary_hypertension|_primary|_4|KCNK3-related_disorder": 1,
    "not_provided|Pulmonary_hypertension|_primary|_4": 3,
    "Pulmonary_arterial_hypertension": 91,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_hypertension|_primary|_4": 1,
    "Pulmonary_hypertension|_primary|_4|not_provided|Inborn_genetic_diseases": 1,
    "Pulmonary_hypertension|_primary|_4|not_provided": 2,
    "not_specified|not_provided|Pulmonary_hypertension|_primary|_4": 1,
    "Ritscher-Schinzel_syndrome_4": 10,
    "DPYSL5-related_disorder": 5,
    "Ritscher-Schinzel_syndrome_4|not_provided|DPYSL5-related_disorder": 1,
    "not_specified|Dandy-Walker_syndrome|Syndrome_with_a_Dandy-Walker_malformation_as_major_feature|Ritscher-Schinzel_syndrome_1|Ritscher-Schinzel_syndrome_4": 1,
    "not_provided|DPYSL5-related_disorder": 1,
    "DPYSL5-related_disorder|Inborn_genetic_diseases": 1,
    "Ritscher-Schinzel_syndrome_4|Inborn_genetic_diseases": 1,
    "AGBL5-related_disorder": 2,
    "Inborn_genetic_diseases|Retinal_dystrophy": 33,
    "Retinitis_pigmentosa_75": 3,
    "not_provided|AGBL5-related_disorder": 2,
    "not_provided|Retinitis_pigmentosa_75": 2,
    "Retinitis_pigmentosa_75|not_provided": 3,
    "Late-onset_cone-rod_dystrophy": 1,
    "AGBL5-related_disorder|not_provided": 3,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_75": 1,
    "not_provided|Retinal_dystrophy|AGBL5-related_disorder": 1,
    "Retinitis_pigmentosa_75|Inborn_genetic_diseases|not_provided": 1,
    "EMILIN1-related_disorder": 9,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_10|Inborn_genetic_diseases": 1,
    "not_provided|Arterial_tortuosity|Arterial_tortuosity-bone_fragility_syndrome": 1,
    "Arterial_tortuosity": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_10": 3,
    "Arterial_tortuosity-bone_fragility_syndrome|Arterial_tortuosity": 2,
    "EMILIN1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|EMILIN1-related_disorder": 1,
    "Arterial_tortuosity|Arterial_tortuosity-bone_fragility_syndrome": 1,
    "not_provided|EMILIN1-related_disorder": 2,
    "EMILIN1-related_disorder|Inborn_genetic_diseases": 1,
    "EMILIN-1-related_connective_tissue_disease|Inborn_genetic_diseases|not_provided": 1,
    "Essential_fructosuria|not_provided": 13,
    "Essential_fructosuria": 57,
    "KHK-related_disorder|Essential_fructosuria": 2,
    "KHK-related_disorder": 4,
    "not_specified|Essential_fructosuria": 4,
    "Essential_fructosuria|not_specified": 3,
    "Essential_fructosuria|KHK-related_disorder": 1,
    "not_provided|Essential_fructosuria": 2,
    "Peripheral_motor_neuropathy|_childhood-onset|_biotin-responsive|SLC5A6-related_disorder|not_provided|Neurodegeneration|_infantile-onset|_biotin-responsive": 1,
    "not_provided|Neurodegeneration|_infantile-onset|_biotin-responsive": 1,
    "Neurodegeneration|_infantile-onset|_biotin-responsive": 6,
    "SLC5A6-related_disorder": 4,
    "Neurodegeneration|_infantile-onset|_biotin-responsive|Peripheral_motor_neuropathy|_childhood-onset|_biotin-responsive": 1,
    "Neurodegeneration|_infantile-onset|_biotin-responsive|not_provided|Inborn_genetic_diseases": 1,
    "Neurodegeneration|_infantile-onset|_biotin-responsive|SLC5A6-related_disorder": 1,
    "not_provided|Peripheral_motor_neuropathy|_childhood-onset|_biotin-responsive": 1,
    "Neurodegeneration|_infantile-onset|_biotin-responsive|not_provided": 1,
    "Neurodegeneration|_infantile-onset|_biotin-responsive|Peripheral_motor_neuropathy|_childhood-onset|_biotin-responsive|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_50|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_50|not_provided": 18,
    "Developmental_and_epileptic_encephalopathy|_50": 24,
    "not_provided|Developmental_and_epileptic_encephalopathy|_50": 12,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_50": 2,
    "not_provided|CAD-related_disorder|Inborn_genetic_diseases": 3,
    "CAD-related_disorder|not_provided": 23,
    "not_provided|CAD-related_disorder": 11,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_50": 2,
    "Coronary_artery_disease|_autosomal_dominant_2|Inborn_genetic_diseases|not_provided": 1,
    "CAD-related_disorder": 3,
    "Infantile_epileptic_dyskinetic_encephalopathy|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_50|not_specified|not_provided": 1,
    "Infantile_epileptic_dyskinetic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_50|not_provided": 2,
    "CAD-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_50": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_50|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_50|not_specified|not_provided": 1,
    "Coronary_artery_disease|_autosomal_dominant_2": 3,
    "Developmental_and_epileptic_encephalopathy|_50|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_50|not_provided|CAD-related_disorder": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_50|not_specified|not_provided|CAD-related_disorder": 1,
    "Infantile_epileptic_dyskinetic_encephalopathy|not_provided|CAD-related_disorder": 1,
    "Infantile_epileptic_dyskinetic_encephalopathy|Developmental_and_epileptic_encephalopathy|_50|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CAD-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_50|Intellectual_disability|Epilepsy|Congenital_anomaly_of_face": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_50|not_specified": 1,
    "Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|not_specified": 1,
    "TRIM54-related_disorder": 5,
    "TRIM54-related_disorder|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 30,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 2,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)": 3,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome": 2,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided": 5,
    "MPV17-related_disorder": 6,
    "Mitochondrial_DNA_depletion_syndrome|_hepatocerebral_form": 14,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 11,
    "not_provided|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 4,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided|MPV17-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|not_provided|MPV17-related_disorder": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 4,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 4,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided": 5,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_hepatocerebral_form": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 6,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome|_hepatocerebral_form|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|not_provided|MPV17-related_mitochondrial_DNA_maintenance_defect|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|not_provided": 5,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 2,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|not_provided": 2,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided|Mitochondrial_DNA_depletion_syndrome": 1,
    "MPV17-related_disorder|not_provided|Mitochondrial_DNA_depletion_syndrome|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome|not_provided": 2,
    "not_provided|MPV17-related_disorder|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|MPV17-related_disorder|not_specified|not_provided": 1,
    "MPV17-related_disorder|not_provided": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|MPV17-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|MPV17-related_mitochondrial_DNA_maintenance_defect|not_provided|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided": 2,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|not_provided|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)": 1,
    "MPV17-related_disorder|not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 1,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_provided|Mitochondrial_DNA_depletion_syndrome": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|MPV17-related_disorder|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_disease|MPV17-related_disorder|Mitochondrial_DNA_depletion_syndrome|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome": 19,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|MPV17-related_disorder|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_type_2EE|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 2,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)": 4,
    "Mitochondrial_DNA_depletion_syndrome|not_provided": 4,
    "not_provided|MPV17-related_disorder|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome|_hepatocerebral_form|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided|MPV17-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_DNA_depletion_syndrome_6_(hepatocerebral_type)|not_specified|MPV17-related_disorder": 1,
    "not_provided|EIF2B4-related_disorder|Vanishing_white_matter_disease": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_4": 2,
    "Leukoencephalopathy_with_vanishing_white_matter_4": 7,
    "Leukoencephalopathy_with_vanishing_white_matter_4|Inborn_genetic_diseases": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_4|not_provided": 1,
    "not_specified|EIF2B4-related_disorder|not_provided|Vanishing_white_matter_disease": 1,
    "Vanishing_white_matter_disease|not_provided|not_specified": 2,
    "not_provided|Leukoencephalopathy_with_vanishing_white_matter_4": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_4|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Vanishing_white_matter_disease": 3,
    "EIF2B4-related_disorder|not_provided|Vanishing_white_matter_disease": 1,
    "Inborn_genetic_diseases|EIF2B4-related_disorder": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_4|Vanishing_white_matter_disease|not_provided|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "not_provided|EIF2B4-related_disorder": 2,
    "not_provided|Leukoencephalopathy_with_vanishing_white_matter_1": 4,
    "not_provided|Leukoencephalopathy_with_vanishing_white_matter_1|Leukoencephalopathy_with_vanishing_white_matter_4|Vanishing_white_matter_disease|Inborn_genetic_diseases": 1,
    "not_provided|Vanishing_white_matter_disease|Inborn_genetic_diseases": 2,
    "Vanishing_white_matter_disease|Inborn_genetic_diseases": 5,
    "EIF2B4-related_disorder": 1,
    "Vanishing_white_matter_disease|EIF2B4-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Vanishing_white_matter_disease": 2,
    "SNX17-related_disorder": 3,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|not_provided": 2,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant": 8,
    "not_provided|Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_Pigmentosa|_Dominant|not_specified": 1,
    "not_specified|ZNF513-related_disorder": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_Pigmentosa|_Dominant": 1,
    "not_provided|ZNF513-related_disorder": 3,
    "ZNF513-related_disorder": 2,
    "Retinitis_pigmentosa_58|not_provided": 2,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|not_provided|not_specified": 1,
    "ZNF513-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|not_specified": 2,
    "Retinitis_pigmentosa_58|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|Retinal_dystrophy|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_58": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_58|Optic_atrophy|ZNF513-related_disorder|Retinal_dystrophy|not_specified": 1,
    "not_specified|Retinitis_pigmentosa|not_provided": 9,
    "not_specified|Retinitis_Pigmentosa|_Dominant|not_provided": 1,
    "Retinitis_pigmentosa_58": 2,
    "ZNF513-related_disorder|Retinitis_pigmentosa": 1,
    "Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 573,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 61,
    "IFT172-related_disorder": 124,
    "not_provided|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|Retinitis_pigmentosa": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|Retinal_dystrophy": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 3,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 19,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|not_provided": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 8,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Retinal_dystrophy": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 46,
    "IFT172-related_disorder|not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 3,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided": 12,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71": 105,
    "Retinal_dystrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder": 32,
    "Retinitis_pigmentosa_71": 6,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinal_dystrophy": 1,
    "IFT172-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 3,
    "IFT172-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20": 2,
    "not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 7,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 6,
    "not_provided|IFT172-related_disorder": 3,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy": 5,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder": 3,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided": 2,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder|not_provided": 1,
    "IFT172-related_disorder|not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 7,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|not_specified": 1,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 11,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|not_provided|IFT172-related_disorder": 3,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|not_provided": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_specified": 4,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|not_provided": 2,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|not_specified": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 249,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 5,
    "Joubert_syndrome|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_specified": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|Bardet-Biedl_syndrome_20": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|IFT172-related_disorder": 2,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinal_dystrophy": 3,
    "Short-rib_thoracic_dysplasia_10_without_polydactyly|not_provided": 2,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Inborn_genetic_diseases": 3,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 11,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 6,
    "not_specified|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder": 22,
    "Retinal_dystrophy|Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|IFT172-related_disorder": 6,
    "not_provided|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder": 2,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|IFT172-related_disorder": 3,
    "Bardet-Biedl_syndrome_20": 3,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20": 18,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 6,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided|Retinal_dystrophy|IFT172-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|not_provided": 1,
    "IFT172-related_disorder|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 6,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|IFT172-related_disorder": 6,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|not_specified|not_provided": 2,
    "not_provided|IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|Retinal_dystrophy|IFT172-related_disorder": 1,
    "Inborn_genetic_diseases|IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 6,
    "IFT172-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 2,
    "not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_specified|IFT172-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|not_provided|IFT172-related_disorder|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder": 7,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder": 3,
    "Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 7,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 2,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 2,
    "Short-rib_thoracic_dysplasia_10_with_polydactyly|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|Anophthalmia-microphthalmia_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 18,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 3,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|Inborn_genetic_diseases": 2,
    "IFT172-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "IFT172-related_disorder|not_provided": 2,
    "not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder": 2,
    "not_provided|Retinal_dystrophy|Inborn_genetic_diseases|IFT172-related_disorder|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified|not_provided|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_1": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|Bardet-Biedl_syndrome_20": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|IFT172-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|not_provided|IFT172-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "IFT172-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|Bardet-Biedl_syndrome_20|Neurodevelopmental_disorder|not_specified|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified|not_provided": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified|Bardet-Biedl_syndrome_20|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|not_provided|IFT172-related_disorder": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Intellectual_disability": 1,
    "Short-rib_thoracic_dysplasia_10_without_polydactyly": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder|not_specified": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|IFT172-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 2,
    "IFT172-related_disorder|Bardet-Biedl_syndrome|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Retinal_dystrophy|IFT172-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified|Bardet-Biedl_syndrome_20": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder": 3,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Retinal_dystrophy": 2,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20": 4,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|IFT172-related_disorder|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Retinal_dystrophy": 2,
    "not_specified|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|not_specified": 1,
    "not_specified|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|not_provided": 4,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Inborn_genetic_diseases": 2,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 3,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 4,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|IFT172-related_disorder": 3,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Retinal_dystrophy": 2,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Short-rib_thoracic_dysplasia_10_without_polydactyly|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 1,
    "IFT172-related_disorder|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|Bardet-Biedl_syndrome_22": 1,
    "IFT172-related_disorder|not_provided|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|IFT172-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Bardet-Biedl_syndrome_20": 1,
    "not_provided|IFT172-related_disorder|Optic_atrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|not_provided|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_1": 1,
    "IFT172-related_disorder|not_specified|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_polydactyly|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "Retinal_dystrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_specified|IFT172-related_disorder|not_provided|Bardet-Biedl_syndrome_20": 1,
    "IFT172-related_disorder|Bardet-Biedl_syndrome_20|not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome_20": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|IFT172-related_disorder|Bardet-Biedl_syndrome_20": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|Bardet-Biedl_syndrome_22": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|IFT172-related_disorder": 3,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|not_provided|not_specified": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified|not_provided|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Nephronophthisis": 1,
    "Inborn_genetic_diseases|IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|not_provided": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 2,
    "not_specified|not_provided|IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71": 2,
    "Bardet-Biedl_syndrome|not_provided|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder|Bardet-Biedl_syndrome_20": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|not_provided|Retinal_dystrophy": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|not_specified|Bardet-Biedl_syndrome_20|not_provided|IFT172-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_10_without_polydactyly|not_provided|IFT172-related_disorder": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|IFT172-related_disorder|not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "not_specified|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|Retinal_dystrophy|IFT172-related_disorder": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "not_specified|IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|IFT172-related_disorder": 1,
    "not_provided|IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Retinal_dystrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|not_specified": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_provided|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases": 1,
    "IFT172-related_disorder|Inborn_genetic_diseases|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Inborn_genetic_diseases|IFT172-related_disorder|not_provided": 1,
    "not_provided|not_specified|IFT172-related_disorder|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71": 1,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinal_dystrophy": 1,
    "not_provided|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|not_specified": 1,
    "not_provided|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|IFT172-related_disorder|Bardet-Biedl_syndrome_20": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|IFT172-related_disorder|Bardet-Biedl_syndrome_20": 2,
    "IFT172-related_disorder|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Optic_atrophy|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome_20": 1,
    "Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Inborn_genetic_diseases|Bardet-Biedl_syndrome_20|IFT172-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|IFT172-related_disorder|Retinal_dystrophy": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Bardet-Biedl_syndrome_20|not_provided|Inborn_genetic_diseases|IFT172-related_disorder": 1,
    "Bardet-Biedl_syndrome_20|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Retinal_dystrophy|IFT172-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly|Retinitis_pigmentosa_71|Inborn_genetic_diseases|Retinal_dystrophy|Bardet-Biedl_syndrome_20": 1,
    "IFT172-related_disorder|not_provided|Bardet-Biedl_syndrome_20|Retinitis_pigmentosa_71|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "FASTING_PLASMA_GLUCOSE_LEVEL_QUANTITATIVE_TRAIT_LOCUS_5|not_provided": 2,
    "GCKR-related_disorder|not_provided|FASTING_PLASMA_GLUCOSE_LEVEL_QUANTITATIVE_TRAIT_LOCUS_5": 1,
    "GCKR-related_disorder": 3,
    "FASTING_PLASMA_GLUCOSE_LEVEL_QUANTITATIVE_TRAIT_LOCUS_5|Hypertriglyceridemia|not_provided|not_specified": 1,
    "FASTING_PLASMA_GLUCOSE_LEVEL_QUANTITATIVE_TRAIT_LOCUS_5": 2,
    "not_provided|GCKR-related_disorder": 1,
    "not_provided|FASTING_PLASMA_GLUCOSE_LEVEL_QUANTITATIVE_TRAIT_LOCUS_5": 6,
    "GCKR-related_disorder|not_provided": 1,
    "Fischer-Zirnsak_progeroid_syndrome": 2,
    "Aplasia_cutis-enamel_dysplasia_syndrome": 5,
    "not_provided|RASopathy|Cardiovascular_phenotype|not_specified": 3,
    "Noonan_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "PPP1CB-related_disorder": 3,
    "not_specified|not_provided|RASopathy|PPP1CB-related_disorder|Noonan_syndrome-like_disorder_with_loose_anagen_hair_2": 1,
    "PPP1CB-related_disorder|not_provided": 1,
    "not_provided|PPP1CB-related_disorder": 2,
    "not_provided|RASopathy|Noonan_syndrome|Cardiovascular_phenotype|Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|Inborn_genetic_diseases|Neurodevelopmental_delay|Dandy-Walker_syndrome": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|RASopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|PPP1CB-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair_2": 1,
    "not_provided|PPP1CB-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|PPP1CB-related_disorder": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_2": 5,
    "not_specified|not_provided|PPP1CB-related_disorder": 1,
    "Noonan_syndrome|not_provided": 23,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|Noonan_syndrome|not_provided": 1,
    "RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair|Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|not_provided|Cardiovascular_phenotype": 1,
    "RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|Cardiovascular_phenotype|not_provided": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|not_provided": 1,
    "PPP1CB-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_2|not_provided|RASopathy|PPP1CB-related_disorder": 1,
    "PPP1CB-related_disorder|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|PPP1CB-related_disorder": 1,
    "Retinitis_pigmentosa_54|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_54|not_provided": 2,
    "not_provided|PCARE-related_disorder|Retinitis_pigmentosa_54": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_54": 2,
    "not_specified|not_provided|Retinitis_pigmentosa_54|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|Retinitis_pigmentosa_54|Optic_atrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_54|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa|not_specified|not_provided": 15,
    "Retinitis_pigmentosa_54|Retinal_dystrophy": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_54|Retinitis_pigmentosa_with_macular_involvement": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 23,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_54|not_specified": 1,
    "Retinitis_pigmentosa_54|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_54": 2,
    "Retinitis_pigmentosa|not_provided|not_specified": 8,
    "not_provided|Retinitis_pigmentosa_54|not_specified": 1,
    "Retinitis_pigmentosa_54": 12,
    "PCARE-related_disorder|not_provided": 4,
    "not_specified|not_provided|Retinitis_pigmentosa_54": 1,
    "not_specified|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 2,
    "Cone-rod_dystrophy_23": 1,
    "not_provided|PCARE-related_disorder": 6,
    "not_provided|Retinitis_pigmentosa_54": 4,
    "Retinitis_pigmentosa_54|Retinitis_pigmentosa|See_cases|PCARE-related_disorder|Retinal_dystrophy|not_provided": 1,
    "PCARE-related_disorder|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_54": 1,
    "Retinitis_pigmentosa_54|not_provided|Retinitis_pigmentosa": 3,
    "not_provided|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_54": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|PCARE-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_54": 1,
    "Retinitis_pigmentosa_54|not_provided": 4,
    "PCARE-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_54": 1,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|Optic_atrophy|not_provided": 1,
    "Optic_atrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_54|Retinitis_pigmentosa|not_provided|Retinal_dystrophy|not_specified": 1,
    "PCARE-related_disorder": 3,
    "Retinitis_pigmentosa|not_provided|PCARE-related_disorder": 1,
    "Retinal_dystrophy|not_specified|Retinitis_pigmentosa_54|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|PCARE-related_disorder|not_specified": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_54|Retinitis_pigmentosa": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_54": 1,
    "not_provided|Retinitis_pigmentosa|not_specified": 16,
    "not_provided|Retinitis_pigmentosa_54|not_specified|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_23|not_provided|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_54|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 2,
    "Retinal_dystrophy|PCARE-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 3,
    "Retinitis_pigmentosa_54|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 3,
    "Retinitis_pigmentosa_54|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_54|not_specified|Retinitis_pigmentosa|PCARE-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_54": 2,
    "Retinitis_pigmentosa_54|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Stargardt_disease|Retinitis_pigmentosa_54|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa": 19,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_54": 1,
    "not_provided|Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa_54|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|maculopathy": 3,
    "PCARE-related_retinopathy|not_provided|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_54|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases": 7,
    "not_specified|not_provided|Retinitis_pigmentosa": 33,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_54": 1,
    "Neuroblastoma_Susceptibility": 2,
    "Neuroblastoma|_susceptibility_to|_3": 2083,
    "not_provided|Neuroblastoma|_susceptibility_to|_3": 24,
    "not_provided|Neuroblastoma_Susceptibility": 1,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 64,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1057,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 807,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 35,
    "Neuroblastoma|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 44,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neuroblastoma|_susceptibility_to|_3": 3,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Neuroblastoma|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|ALK-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3": 90,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neuroblastoma|_susceptibility_to|_3": 9,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder": 1,
    "ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 5,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3|not_specified": 1,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|Squamous_cell_lung_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Neuroblastoma|_susceptibility_to|_3": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_provided": 46,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 2,
    "Neuroblastoma|_susceptibility_to|_3|not_provided": 11,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 43,
    "Neuroblastoma|_susceptibility_to|_3|Squamous_cell_lung_carcinoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3": 7,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|Squamous_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Neuroblastoma|_susceptibility_to|_3|Ovarian_cancer": 1,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|Squamous_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|not_provided|Neuroblastoma|_susceptibility_to|_3|Neuroblastoma_Susceptibility|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdomyosarcoma": 3,
    "ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neuroblastoma|_susceptibility_to|_3": 3,
    "Neuroblastoma|_susceptibility_to|_3|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|not_specified|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|ALK-related_disorder": 4,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|Squamous_cell_lung_carcinoma|not_provided": 1,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 6,
    "Neuroblastoma|_susceptibility_to|_3|Pseudo-fractures": 1,
    "not_specified|Neuroblastoma|_susceptibility_to|_3": 4,
    "Familial_isolated_pituitary_adenoma|not_specified|not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|Neuroblastoma|_susceptibility_to|_3": 1,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Lung_cancer": 39,
    "ALK-related_disorder": 2,
    "ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neuroblastoma|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Squamous_cell_lung_carcinoma|not_provided|Neuroblastoma|_susceptibility_to|_3": 1,
    "Neuroblastoma|_susceptibility_to|_3|not_specified": 3,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|not_specified": 1,
    "not_specified|not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1,
    "ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_provided": 4,
    "not_specified|Familial_isolated_pituitary_adenoma|Neuroblastoma|_susceptibility_to|_3": 1,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Neuroblastoma|_susceptibility_to|_3|Phonic_tics": 1,
    "ALK-related_disorder|not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 6,
    "Neuroblastoma|_susceptibility_to|_3|not_provided|Familial_isolated_pituitary_adenoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_3|Familial_isolated_pituitary_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_3|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3": 2,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3": 3,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|ALK-related_disorder": 1,
    "ALK-related_disorder|Familial_isolated_pituitary_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1,
    "Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder": 2,
    "not_provided|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|ALK-related_disorder|not_provided|not_specified|Neuroblastoma|_susceptibility_to|_3": 1,
    "Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neuroblastoma|_susceptibility_to|_3": 2,
    "Familial_isolated_pituitary_adenoma|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Neuroblastoma|_susceptibility_to|_3|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Neuroblastoma|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Neuroblastoma_Susceptibility|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3": 2,
    "Hereditary_cancer-predisposing_syndrome|ALK-related_disorder|not_provided|Neuroblastoma|_susceptibility_to|_3": 1,
    "ALK-related_disorder|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3": 1,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_3|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 1,
    "Familial_isolated_pituitary_adenoma|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3": 1,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|ALK-related_disorder|not_provided": 1,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neuroblastoma|_susceptibility_to|_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|Ovarian_cancer": 1,
    "Neuroblastoma|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_isolated_pituitary_adenoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_provided|ALK-related_disorder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_provided": 1,
    "Neuroblastoma|_susceptibility_to|_3|Familial_isolated_pituitary_adenoma": 1,
    "Neuroblastoma|_susceptibility_to|_3|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|ALK-related_disorder": 1,
    "Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|ALK-related_disorder|not_specified|not_provided": 2,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|not_provided": 1,
    "not_specified|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_provided": 1,
    "ALK-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Neuroblastoma|_susceptibility_to|_3": 1,
    "ALK-related_disorder|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|ALK-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|not_specified": 2,
    "ALK-related_disorder|not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_3|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|not_provided": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_3": 1,
    "Familial_isolated_pituitary_adenoma": 3,
    "Neuroblastoma|_susceptibility_to|_3|ALK-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Neuroblastoma|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|ALK-related_disorder|not_specified": 1,
    "ALK-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "GALNT14-related_disorder": 3,
    "not_provided|Amyotrophic_lateral_sclerosis": 9,
    "Hereditary_xanthinuria_type_1": 226,
    "Hereditary_xanthinuria_type_1|not_provided": 8,
    "not_provided|Hereditary_xanthinuria_type_1": 3,
    "Xanthinuria": 4,
    "Xanthinuria_type_II": 568,
    "Hereditary_xanthinuria_type_1|Inborn_genetic_diseases": 10,
    "Hereditary_xanthinuria_type_1|Xanthinuria_type_II": 62,
    "Xanthinuria_type_II|Hereditary_xanthinuria_type_1": 41,
    "Xanthinuria_type_II|not_provided|Hereditary_xanthinuria_type_1": 9,
    "Inborn_genetic_diseases|Xanthinuria_type_II|XDH-related_disorder": 1,
    "Xanthinuria_type_II|Inborn_genetic_diseases|Hereditary_xanthinuria_type_1": 4,
    "Hereditary_xanthinuria_type_1|XDH-related_disorder|Xanthinuria_type_II|not_provided": 2,
    "Xanthinuria_type_II|XDH-related_disorder|not_provided|Hereditary_xanthinuria_type_1": 2,
    "Hereditary_xanthinuria_type_1|Xanthinuria_type_II|XDH-related_disorder": 3,
    "Xanthinuria_type_II|not_provided": 12,
    "Xanthinuria_type_II|Hereditary_xanthinuria_type_1|Inborn_genetic_diseases": 4,
    "Hereditary_xanthinuria_type_1|XDH-related_disorder|Xanthinuria_type_II": 2,
    "XDH-related_disorder": 6,
    "XDH-related_disorder|Xanthinuria_type_II": 2,
    "Hereditary_xanthinuria_type_1|Xanthinuria_type_II|not_provided": 6,
    "Hereditary_xanthinuria_type_1|not_specified|Xanthinuria_type_II|not_provided": 1,
    "Xanthinuria_type_II|Inborn_genetic_diseases": 4,
    "not_provided|Hereditary_xanthinuria_type_1|Xanthinuria_type_II|not_specified": 2,
    "Xanthinuria_type_II|Hereditary_xanthinuria_type_1|not_provided": 5,
    "Xanthinuria_type_II|not_provided|Hereditary_xanthinuria_type_1|not_specified|XDH-related_disorder": 1,
    "Inborn_genetic_diseases|Xanthinuria_type_II": 6,
    "Hereditary_xanthinuria_type_1|not_provided|Xanthinuria_type_II": 2,
    "Hereditary_xanthinuria_type_1|Xanthinuria_type_II|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_xanthinuria_type_1": 10,
    "Xanthinuria_type_II|not_specified|not_provided|Hereditary_xanthinuria_type_1": 1,
    "Xanthinuria_type_II|XDH-related_disorder|Hereditary_xanthinuria_type_1": 4,
    "Hereditary_xanthinuria_type_1|not_specified": 1,
    "not_provided|Xanthinuria_type_II|Hereditary_xanthinuria_type_1": 6,
    "not_specified|Hereditary_xanthinuria_type_1|Xanthinuria_type_II|not_provided": 2,
    "not_specified|Hereditary_xanthinuria_type_1|Xanthinuria_type_II|XDH-related_disorder": 1,
    "not_provided|Xanthinuria_type_II": 20,
    "Xanthinuria_type_II|Xanthinuria": 1,
    "Hereditary_xanthinuria_type_1|Xanthinuria_type_II|Inborn_genetic_diseases": 7,
    "not_specified|XDH-related_disorder|Hereditary_xanthinuria_type_1|Xanthinuria_type_II": 1,
    "Hereditary_xanthinuria_type_1|not_specified|Xanthinuria_type_II|XDH-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Xanthinuria_type_II|Hereditary_xanthinuria_type_1": 1,
    "Inborn_genetic_diseases|not_provided|Xanthinuria_type_II|Hereditary_xanthinuria_type_1": 1,
    "not_provided|Hereditary_xanthinuria_type_1|not_specified|Xanthinuria_type_II": 2,
    "Hereditary_xanthinuria_type_1|Inborn_genetic_diseases|Xanthinuria_type_II": 4,
    "not_provided|Hereditary_xanthinuria_type_1|Xanthinuria_type_II": 1,
    "Xanthinuria_type_II|Hereditary_xanthinuria_type_1|XDH-related_disorder": 1,
    "XDH-related_disorder|Hereditary_xanthinuria_type_1|Xanthinuria_type_II": 4,
    "Xanthinuria_type_II|Hereditary_xanthinuria_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Xanthinuria_type_II|Hereditary_xanthinuria_type_1|XDH-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_xanthinuria_type_1|Xanthinuria_type_II|not_provided": 1,
    "Xanthinuria_type_II|XDH-related_disorder": 1,
    "not_specified|Xanthinuria_type_II": 21,
    "not_provided|XDH-related_disorder": 1,
    "Hereditary_xanthinuria_type_1|XDH-related_disorder|Xanthinuria_type_II|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Xanthinuria_type_II": 1,
    "XDH-related_disorder|Xanthinuria_type_II|Hereditary_xanthinuria_type_1|not_provided": 1,
    "Hereditary_xanthinuria_type_1|XDH-related_disorder|not_provided|not_specified|Xanthinuria_type_II": 1,
    "Inborn_genetic_diseases|Xanthinuria_type_II|Hereditary_xanthinuria_type_1": 1,
    "Xanthinuria_type_II|not_provided|Inborn_genetic_diseases": 1,
    "3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|not_provided": 18,
    "3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 212,
    "not_provided|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 21,
    "SRD5A2-related_disorder": 3,
    "SRD5A2-related_disorder|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 4,
    "not_specified|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|not_provided": 1,
    "See_cases|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 1,
    "3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|not_provided|not_specified": 4,
    "SRD5A2-related_disorder|not_provided|Autism_spectrum_disorder|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|Micropenis": 1,
    "3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|not_specified": 5,
    "SRD5A2-related_disorder|not_provided|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 2,
    "3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "Abnormality_of_the_genitourinary_system|not_provided|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 1,
    "SRD5A2-related_disorder|not_provided|SRD5A2_POLYMORPHISM|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 1,
    "Micropenis": 1,
    "not_specified|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency": 1,
    "not_provided|3-Oxo-5_alpha-steroid_delta_4-dehydrogenase_deficiency|SRD5A2-related_disorder": 1,
    "Hereditary_spastic_paraplegia_4": 743,
    "Spastic_paraplegia|_autosomal_dominant": 46,
    "Hereditary_spastic_paraplegia_4|not_provided|SPAST-related_disorder|not_specified": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4": 14,
    "Hereditary_spastic_paraplegia_4|not_provided": 60,
    "not_provided|Hereditary_spastic_paraplegia_4": 102,
    "not_specified|Hereditary_spastic_paraplegia_4": 9,
    "Hereditary_spastic_paraplegia_4|Inborn_genetic_diseases": 11,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4": 7,
    "SPAST-related_disorder|Hereditary_spastic_paraplegia_4": 8,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_4": 14,
    "SPAST-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia_4|.|Hereditary_spastic_paraplegia|Cerebral_palsy": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4|.": 1,
    "Inborn_genetic_diseases|SPAST-related_disorder|Hereditary_spastic_paraplegia_4": 1,
    "Hereditary_spastic_paraplegia_4|not_specified": 7,
    "SPAST-related_disorder|Hereditary_spastic_paraplegia_4|not_provided": 1,
    "Hereditary_spastic_paraplegia_4|Hereditary_spastic_paraplegia": 4,
    "SPAST-related_disorder|not_provided|Hereditary_spastic_paraplegia_4": 2,
    "SPAST-related_disorder|not_provided": 1,
    "SPAST-related_disorder": 5,
    "Hereditary_spastic_paraplegia_4|Hereditary_spastic_paraplegia|SPAST-related_disorder|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_4|Spastic_paraplegia": 2,
    "not_provided|SPAST-related_disorder|Hereditary_spastic_paraplegia_4|Spastic_paraplegia|_autosomal_dominant|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia_4|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_4": 3,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_4": 3,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_4|Hereditary_spastic_paraplegia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_4|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_4|Fatigue|Abnormal_myelination|Seizure|not_provided": 1,
    "SPAST-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_4|not_provided": 1,
    "Hereditary_spastic_paraplegia_4|SPAST-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_4": 1,
    "Hereditary_spastic_paraplegia_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|SPAST-related_spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_4": 1,
    "SPAST-related_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_4|Flexion_contracture|Tip-toe_gait|Pes_valgus|Spasticity|Spastic_diplegia": 1,
    "Hereditary_spastic_paraplegia_2": 164,
    "not_provided|Hereditary_spastic_paraplegia_4|Tics": 1,
    "not_specified|Hereditary_spastic_paraplegia": 7,
    "Hereditary_spastic_paraplegia_4|not_provided|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_4|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_4|Tip-toe_gait": 1,
    "not_provided|Hereditary_spastic_paraplegia_4|not_specified": 1,
    "Hereditary_spastic_paraplegia_4|Spastic_paraparesis": 1,
    "Motor_tics": 1,
    "SPAST-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia_4": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4|Spastic_paraparesis": 1,
    "Abnormal_central_motor_function|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|SPAST-related_disorder|Hereditary_spastic_paraplegia_4": 1,
    "not_specified|Hereditary_spastic_paraplegia_4|not_provided": 1,
    "Spastic_diplegia|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_4": 1,
    "Spastic_paraparesis": 3,
    "SPAST-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4": 1,
    "Spasticity|Hereditary_spastic_paraplegia_4": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4|Spastic_paraplegia|Spastic_ataxia": 1,
    "not_provided|Hereditary_spastic_paraplegia_4|Spastic_paraplegia": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_4": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_4|not_provided": 1,
    "Spastic_paraplegia|_autosomal_dominant|not_specified": 2,
    "not_provided|Spastic_paraplegia|_autosomal_dominant": 4,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 418,
    "Inborn_genetic_diseases|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 21,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Inborn_genetic_diseases": 13,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 130,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Autoinflammatory_syndrome": 3,
    "NLRC4-related_disorder": 4,
    "not_provided|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 9,
    "NLRC4-related_disorder|Autoinflammatory_syndrome|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 2,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autoinflammatory_syndrome|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 11,
    "Familial_cold_autoinflammatory_syndrome_4": 6,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_specified|not_provided": 2,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Autoinflammatory_syndrome": 6,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_provided": 14,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Autoinflammatory_syndrome|not_provided|NLRC4-related_disorder|not_specified": 1,
    "Autoinflammatory_syndrome|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_specified|not_provided": 1,
    "not_specified|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_specified|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 3,
    "not_provided|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Autoinflammatory_syndrome": 1,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|NLRC4-related_disorder|not_provided": 1,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 4,
    "NLRC4-related_disorder|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_specified|not_provided|Autoinflammatory_syndrome": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_provided": 6,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_specified": 4,
    "See_cases|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_specified|not_provided|NLRC4-related_disorder|Autoinflammatory_syndrome": 1,
    "not_provided|Autoinflammatory_syndrome|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_specified|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 4,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|NLRC4-related_disorder": 1,
    "NLRC4-related_disorder|not_provided|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "NLRC4-related_disorder|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Atopic_eczema": 1,
    "Inborn_genetic_diseases|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_provided": 2,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_provided": 2,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Autoinflammatory_syndrome": 1,
    "not_provided|NLRC4-related_disorder": 1,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 3,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_provided|NLRC4-related_disorder": 2,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|NLRC4-related_disorder": 3,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_specified": 1,
    "NLRC4-related_disorder|Autoinflammatory_syndrome|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Syndrome_of_entercolitis_and_autoinflmmation_caused_by_mutation_of_NLRC4_(SCAN4)|not_provided": 1,
    "Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 5,
    "not_provided|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "NLRC4-related_disorder|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "NLRC4-related_disorder|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|not_specified|not_provided": 1,
    "NLRC4-related_disorder|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_4|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome|Inborn_genetic_diseases": 3,
    "NLRC4-related_disorder|Familial_cold_autoinflammatory_syndrome_4|Periodic_fever-infantile_enterocolitis-autoinflammatory_syndrome": 1,
    "BIRC6-related_disorder": 53,
    "BIRC6-related_disorder|not_provided": 7,
    "not_provided|BIRC6-related_disorder": 19,
    "not_specified|BIRC6-related_disorder": 1,
    "BIRC6-related_disorder|not_specified": 1,
    "Cutis_laxa|_autosomal_recessive|_type_2E": 10,
    "LTBP1-related_disorder": 2,
    "not_specified|Cutis_laxa|_autosomal_recessive|_type_2E": 1,
    "CRIM1-related_disorder": 10,
    "not_provided|CRIM1-related_disorder": 7,
    "CRIM1-related_disorder|not_provided": 7,
    "CRIM1-related_disorder|not_specified": 1,
    "HEATR5B-associated_Pontocerebellar_hypoplasia|Congenital_pontocerebellar_hypoplasia": 2,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay": 21,
    "Neurological_syndrome_with_pontocerebellar_hypoplasia": 1,
    "HEATR5B-related_disorder": 1,
    "Early_onset_and_severe_retinal_dystrophy_with_neurological_impairment_and_facial_dysmorphia": 4,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome": 5,
    "EIF2AK2-related_disorder": 3,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome|Dystonia_33|not_provided": 1,
    "Dystonia_33": 7,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome|Global_developmental_delay|Leukoencephalopathy|Developmental_regression": 1,
    "Inborn_genetic_diseases|EIF2AK2-related_disorder": 1,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome|Cognitive_impairment": 1,
    "not_provided|Inborn_genetic_diseases|Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome": 1,
    "Dystonia_33|Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome": 1,
    "Dystonia_33|not_provided": 1,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome|EIF2AK2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Dystonia_33": 1,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome|Leukoencephalopathy|Global_developmental_delay|Developmental_regression": 2,
    "not_provided|Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome": 1,
    "Leukoencephalopathy|_developmental_delay|_and_episodic_neurologic_regression_syndrome|EIF2AK2-related_disorder": 1,
    "CDC42EP3-related_condition": 1,
    "Irido-corneo-trabecular_dysgenesis|Glaucoma_3A": 27,
    "Glaucoma_3A|Irido-corneo-trabecular_dysgenesis": 48,
    "Glaucoma_3A|Irido-corneo-trabecular_dysgenesis|not_provided": 2,
    "Irido-corneo-trabecular_dysgenesis|Glaucoma_3A|not_provided": 1,
    "Primary_congenital_glaucoma|Irido-corneo-trabecular_dysgenesis": 7,
    "Irido-corneo-trabecular_dysgenesis|Primary_congenital_glaucoma": 5,
    "Irido-corneo-trabecular_dysgenesis|not_provided|Glaucoma_3A": 2,
    "not_provided|Irido-corneo-trabecular_dysgenesis|Glaucoma_3A": 1,
    "not_provided|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis": 1,
    "Irido-corneo-trabecular_dysgenesis|not_provided|Primary_congenital_glaucoma": 1,
    "Congenital_glaucoma": 217,
    "Glaucoma_3A|not_provided|CYP1B1-related_disorder|Congenital_glaucoma|Irido-corneo-trabecular_dysgenesis": 1,
    "Congenital_glaucoma|not_specified": 2,
    "Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6": 3,
    "Inborn_genetic_diseases|Congenital_glaucoma": 2,
    "not_provided|Congenital_glaucoma": 3,
    "Congenital_glaucoma|not_provided": 2,
    "Primary_congenital_glaucoma": 2,
    "not_provided|Congenital_glaucoma|not_specified": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A": 11,
    "CYP1B1-related_disorder|Primary_congenital_glaucoma|Anterior_segment_dysgenesis_6|Glaucoma_3A|Congenital_glaucoma|not_provided": 1,
    "not_provided|Primary_congenital_glaucoma|Congenital_glaucoma|Anterior_segment_dysgenesis_6": 1,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6": 3,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Congenital_glaucoma|not_specified|not_provided": 2,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|not_specified|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Anterior_segment_dysgenesis_6|Congenital_glaucoma": 4,
    "Glaucoma_3A|Primary_congenital_glaucoma": 2,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Congenital_glaucoma|Anterior_segment_dysgenesis|not_provided": 1,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|CYP1B1-related_disorder|Primary_congenital_glaucoma|not_provided": 1,
    "Congenital_glaucoma|Irido-corneo-trabecular_dysgenesis|not_specified|not_provided|Glaucoma_3A": 1,
    "Glaucoma_3A|not_provided": 1,
    "Anterior_segment_dysgenesis_6|not_provided|Congenital_glaucoma|Glaucoma_3A": 1,
    "Anterior_segment_dysgenesis_6|Congenital_glaucoma|not_specified|not_provided|Glaucoma_3A": 1,
    "not_specified|Congenital_glaucoma": 2,
    "not_specified|Glaucoma_3A|not_provided": 1,
    "Primary_congenital_glaucoma|Glaucoma|_primary_open_angle|_juvenile-onset|Glaucoma_3A|Congenital_glaucoma": 1,
    "Glaucoma_3A|Anterior_segment_dysgenesis_6|Congenital_glaucoma|CYP1B1-related_disorder|Anterior_segment_dysgenesis|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Glaucoma_3A|Anterior_segment_dysgenesis_6|not_specified": 1,
    "Congenital_glaucoma|not_provided|Anterior_segment_dysgenesis_6|Glaucoma_3A|Primary_congenital_glaucoma": 1,
    "Anterior_segment_dysgenesis_6|not_provided|Glaucoma_3A|Congenital_glaucoma|Primary_congenital_glaucoma": 1,
    "Glaucoma_3A|Primary_congenital_glaucoma|Congenital_glaucoma|Anterior_segment_dysgenesis_6": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Glaucoma_of_childhood|Congenital_glaucoma|CYP1B1-related_disorder|not_provided|Primary_congenital_glaucoma": 1,
    "Anterior_segment_dysgenesis_6|Congenital_glaucoma|Primary_congenital_glaucoma": 3,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Congenital_glaucoma": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|not_specified": 1,
    "Anterior_segment_dysgenesis_6": 15,
    "CYP1B1-related_disorder|Anterior_segment_dysgenesis_6|Glaucoma_3|_primary_infantile|_B|Glaucoma_3A|Congenital_glaucoma|Myopathy|_centronuclear|_5|not_provided|Irido-corneo-trabecular_dysgenesis|not_specified|Glaucoma|_early-onset|_digenic|Congenital_ocular_coloboma|Primary_congenital_glaucoma": 1,
    "Glaucoma_3A|Anterior_segment_dysgenesis_6|Congenital_glaucoma|Primary_congenital_glaucoma|not_provided": 1,
    "Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|not_provided": 1,
    "Glaucoma_3A|Anterior_segment_dysgenesis_6": 1,
    "Congenital_glaucoma|Primary_congenital_glaucoma|Anterior_segment_dysgenesis_6|Glaucoma_3A": 1,
    "Glaucoma_3A|Irido-corneo-trabecular_dysgenesis|CYP1B1-related_disorder|Congenital_glaucoma|Inborn_genetic_diseases": 1,
    "Glaucoma_3A|Congenital_glaucoma|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|Glaucoma_3A|CYP1B1-related_disorder|not_provided|Primary_congenital_glaucoma": 1,
    "Anterior_segment_dysgenesis_6|Inborn_genetic_diseases": 1,
    "Primary_congenital_glaucoma|Congenital_glaucoma|not_provided|Anterior_segment_dysgenesis_6": 1,
    "Irido-corneo-trabecular_dysgenesis|CYP1B1-related_disorder|Glaucoma_3A|Congenital_glaucoma": 1,
    "Congenital_glaucoma|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|not_specified": 1,
    "CYP1B1-related_disorder": 2,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|Primary_congenital_glaucoma": 1,
    "Primary_congenital_glaucoma|Glaucoma_3A|Anterior_segment_dysgenesis_6|Congenital_glaucoma": 1,
    "Glaucoma_3A|not_specified|Congenital_glaucoma|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|not_provided": 1,
    "Congenital_glaucoma|not_provided|Anterior_segment_dysgenesis_6|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B": 1,
    "Irido-corneo-trabecular_dysgenesis|Congenital_glaucoma|Glaucoma_3A": 1,
    "Congenital_glaucoma|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Glaucoma_3A|not_provided": 1,
    "Anterior_segment_dysgenesis_6|CYP1B1-related_disorder|not_provided|Congenital_ocular_coloboma|Congenital_glaucoma|Glaucoma_3A": 1,
    "not_specified|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|Congenital_glaucoma": 1,
    "Congenital_glaucoma|Irido-corneo-trabecular_dysgenesis|Glaucoma_3A": 2,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|Glaucoma_3A|not_provided": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Congenital_glaucoma|not_provided": 1,
    "Congenital_glaucoma|Inborn_genetic_diseases": 2,
    "not_provided|Anterior_segment_dysgenesis_6": 1,
    "Primary_congenital_glaucoma|Anterior_segment_dysgenesis_6|Glaucoma_3A": 1,
    "not_specified|Congenital_glaucoma|not_provided|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis": 1,
    "Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis|Congenital_glaucoma|not_specified": 1,
    "Primary_congenital_glaucoma|Glaucoma_3A": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Congenital_glaucoma|Primary_congenital_glaucoma": 2,
    "not_provided|Irido-corneo-trabecular_dysgenesis|Congenital_glaucoma|Congenital_ocular_coloboma|not_specified|Glaucoma_3A": 1,
    "Irido-corneo-trabecular_dysgenesis|Glaucoma_3A|Congenital_glaucoma": 1,
    "Congenital_glaucoma|not_provided|CYP1B1-related_disorder": 1,
    "Irido-corneo-trabecular_dysgenesis|Congenital_glaucoma|not_provided|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|Glaucoma_3A|not_specified": 1,
    "Anterior_segment_dysgenesis_6|Primary_congenital_glaucoma|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B": 1,
    "Congenital_glaucoma|not_specified|not_provided|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis": 1,
    "Congenital_glaucoma|CYP1B1-related_disorder|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|Primary_congenital_glaucoma|not_provided": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|not_provided": 1,
    "Congenital_glaucoma|Glaucoma_3A|Anterior_segment_dysgenesis_6|Primary_congenital_glaucoma": 1,
    "Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|not_specified": 1,
    "Congenital_glaucoma|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis": 1,
    "Congenital_glaucoma|not_specified|Glaucoma_3A": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|not_specified": 1,
    "Irido-corneo-trabecular_dysgenesis|Glaucoma_3A|Inborn_genetic_diseases": 1,
    "Irido-corneo-trabecular_dysgenesis|Glaucoma_3A|CYP1B1-related_glaucoma_with_or_without_anterior_segment_dysgenesis|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6": 1,
    "Congenital_glaucoma|not_provided|Anterior_segment_dysgenesis_6": 1,
    "not_specified|Glaucoma_3A": 1,
    "Irido-corneo-trabecular_dysgenesis|Glaucoma_3A|Congenital_glaucoma|not_specified": 1,
    "Anterior_segment_dysgenesis_6|Primary_congenital_glaucoma": 1,
    "not_specified|Irido-corneo-trabecular_dysgenesis|Glaucoma_3A": 1,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|Glaucoma_3A": 1,
    "Congenital_glaucoma|Irido-corneo-trabecular_dysgenesis|Anterior_segment_dysgenesis|not_specified|not_provided|Primary_open_angle_glaucoma|Glaucoma_3A|Congenital_ocular_coloboma": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|Congenital_glaucoma|Glaucoma_3|_primary_infantile|_B|CYP1B1-related_disorder|not_provided|Primary_congenital_glaucoma": 1,
    "Glaucoma|_primary_open_angle|_juvenile-onset|Glaucoma_3A": 1,
    "Glaucoma_3A|Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|Congenital_glaucoma|CYP1B1-related_disorder|Anterior_segment_dysgenesis|not_provided|Irido-corneo-trabecular_dysgenesis": 1,
    "not_provided|Glaucoma|_primary_open_angle|_juvenile-onset|not_specified|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis": 1,
    "Glaucoma_3A|Congenital_glaucoma|CYP1B1-related_disorder|Irido-corneo-trabecular_dysgenesis": 1,
    "Congenital_glaucoma|Anterior_segment_dysgenesis_6|not_specified|not_provided|Glaucoma_3A": 1,
    "CYP1B1-related_disorder|Congenital_glaucoma": 1,
    "Anterior_segment_dysgenesis_6|Congenital_glaucoma|Glaucoma_3A": 1,
    "Primary_congenital_glaucoma|Congenital_glaucoma|Anterior_segment_dysgenesis_6": 1,
    "not_provided|Congenital_glaucoma|Primary_congenital_glaucoma": 1,
    "Anterior_segment_dysgenesis_6|Glaucoma_3A|not_specified|not_provided|Irido-corneo-trabecular_dysgenesis": 1,
    "Glaucoma_3A|not_provided|Irido-corneo-trabecular_dysgenesis": 1,
    "Glaucoma_3|_primary_infantile|_B|Anterior_segment_dysgenesis_6|Glaucoma_3A|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "not_provided|Irido-corneo-trabecular_dysgenesis|Primary_congenital_glaucoma": 1,
    "GALM-related_disorder": 3,
    "GALM-related_disorder|not_provided": 1,
    "not_provided|Galactosemia_4": 1,
    "Galactosemia_4": 3,
    "not_provided|GALM-related_disorder": 2,
    "not_specified|GALM-related_disorder|Galactosemia_4|not_provided": 1,
    "not_provided|GALM-related_disorder|Galactosemia_4": 1,
    "Galactosemia_4|GALM-related_disorder": 1,
    "DHX57-related_disorder": 6,
    "DHX57-related_disorder|not_specified": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4": 66,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1": 9,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided": 3,
    "Fibromatosis|_gingival|_1|not_provided|Noonan_syndrome_4": 7,
    "Gingival_fibromatosis|Noonan_syndrome": 6,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided": 6,
    "Noonan_syndrome|Gingival_fibromatosis": 6,
    "not_provided|Gingival_fibromatosis|Noonan_syndrome": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 5,
    "Gingival_fibromatosis|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|not_specified": 1,
    "Gingival_fibromatosis|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|not_provided": 2,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|Gingival_fibromatosis|not_specified": 1,
    "not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 4,
    "SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|RASopathy": 5,
    "Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 2,
    "Noonan_syndrome_4|not_provided|RASopathy": 2,
    "RASopathy|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "RASopathy|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 7,
    "Cardiovascular_phenotype|Noonan_syndrome_4": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "not_provided|Cardiovascular_phenotype|RASopathy": 13,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|not_specified": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 3,
    "RASopathy|Primary_dilated_cardiomyopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Noonan_syndrome": 1,
    "Noonan_syndrome_4|Cardiovascular_phenotype|not_specified|RASopathy|Fibromatosis|_gingival|_1": 1,
    "not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype": 2,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype": 3,
    "not_specified|RASopathy|Cardiovascular_phenotype": 37,
    "RASopathy|not_specified|Cardiovascular_phenotype": 18,
    "Noonan_syndrome_4": 33,
    "Fibromatosis|_gingival|_1|RASopathy|Noonan_syndrome_4": 2,
    "SOS1-related_disorder": 8,
    "Cardiovascular_phenotype|not_provided|RASopathy": 35,
    "Cardiovascular_phenotype|not_specified|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "not_specified|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 2,
    "RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided|Cardiovascular_phenotype": 1,
    "SOS1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|not_specified|RASopathy": 3,
    "Noonan_syndrome_4|SOS1-related_disorder|Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy": 2,
    "Noonan_syndrome_4|RASopathy|not_specified|Cardiovascular_phenotype|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "SOS1-related_disorder|RASopathy|not_provided|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Noonan_syndrome|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "not_specified|SOS1-related_disorder|not_provided|Cardiovascular_phenotype|RASopathy": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 3,
    "not_provided|Noonan_syndrome_4|not_specified|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Noonan_syndrome_4|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 4,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "not_provided|not_specified|RASopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|SOS1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|Noonan_syndrome_4": 1,
    "Cardiovascular_phenotype|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 3,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy|Cardiovascular_phenotype": 3,
    "RASopathy|SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided|RASopathy": 4,
    "Noonan_syndrome_4|RASopathy|not_provided|Fibromatosis|_gingival|_1": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|RASopathy": 4,
    "not_specified|not_provided|RASopathy": 17,
    "Cardiovascular_phenotype|Noonan_syndrome_4|RASopathy": 3,
    "not_provided|RASopathy|Cardiovascular_phenotype": 20,
    "RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified": 1,
    "RASopathy|not_specified|not_provided|Cardiovascular_phenotype|Noonan_syndrome_4": 1,
    "Noonan_syndrome_4|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|not_provided|RASopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "not_specified|Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 5,
    "Cardiovascular_phenotype|RASopathy|not_provided|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome|not_provided": 3,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 15,
    "Noonan_syndrome_4|not_provided|RASopathy|Cardiovascular_phenotype|not_specified|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Noonan_syndrome_4|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|Fibromatosis|_gingival|_1|RASopathy|not_provided|Noonan_syndrome_4": 1,
    "RASopathy|Noonan_syndrome": 18,
    "not_specified|Cardiovascular_phenotype|RASopathy": 27,
    "not_provided|SOS1-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|not_provided|RASopathy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 13,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_4": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|RASopathy": 2,
    "not_provided|Noonan_syndrome_4": 2,
    "Cardiovascular_phenotype|Noonan_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|Noonan_syndrome|not_provided": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified": 1,
    "not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome": 1,
    "RASopathy|not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|RASopathy": 4,
    "RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|not_specified": 1,
    "Noonan_syndrome_4|Noonan_syndrome|not_specified|not_provided|Fibromatosis|_gingival|_1": 1,
    "not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_4|RASopathy|Fibromatosis|_gingival|_1|not_specified|SOS1-related_disorder": 1,
    "Cardiovascular_phenotype|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 6,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy": 2,
    "not_provided|not_specified|RASopathy|Cardiovascular_phenotype": 5,
    "RASopathy|not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|RASopathy|not_specified": 2,
    "Noonan_syndrome_4|RASopathy": 2,
    "Noonan_syndrome_4|not_specified|not_provided|Cardiovascular_phenotype|RASopathy|Fibromatosis|_gingival|_1": 1,
    "not_specified|not_provided|Noonan_syndrome_4": 1,
    "not_specified|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 3,
    "Cardiovascular_phenotype|SOS1-related_disorder|RASopathy": 1,
    "See_cases|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "not_specified|SOS1-related_disorder|RASopathy|Cardiovascular_phenotype": 1,
    "not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided": 1,
    "Noonan_syndrome_4|not_specified|Cardiovascular_phenotype|RASopathy|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Noonan_syndrome_4": 7,
    "Cardiovascular_phenotype|Noonan_syndrome_4|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 1,
    "not_provided|Primary_dilated_cardiomyopathy|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|not_specified|Noonan_syndrome": 1,
    "not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype": 1,
    "not_provided|Fibromatosis|_gingival|_1|SOS1-related_disorder|Noonan_syndrome_4|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified": 1,
    "RASopathy|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Noonan_syndrome_4|Noonan_syndrome|RASopathy": 1,
    "RASopathy|SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified|RASopathy": 2,
    "Cardiovascular_phenotype|SOS1-related_disorder|RASopathy|not_provided|not_specified": 1,
    "not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|RASopathy": 1,
    "SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|not_provided|Noonan_syndrome": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|RASopathy": 2,
    "SOS1-related_disorder|RASopathy|not_specified|not_provided": 1,
    "Noonan_syndrome_4|RASopathy|not_provided|SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Fibromatosis|_gingival|_1": 1,
    "SOS1-related_disorder|not_provided|RASopathy|Noonan_syndrome": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|not_provided": 1,
    "Fibromatosis|_gingival|_1|RASopathy|not_provided|Noonan_syndrome_4|Cardiovascular_phenotype": 1,
    "not_provided|RASopathy|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|not_specified|Noonan_syndrome_4": 1,
    "not_provided|Noonan_syndrome_4|RASopathy|not_specified|SOS1-related_disorder|Fibromatosis|_gingival|_1": 1,
    "Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|Intellectual_disability|RASopathy|not_provided": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|not_specified|RASopathy|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy": 1,
    "SOS1-related_disorder|RASopathy|Fibromatosis|_gingival|_1": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|SOS1-related_disorder|Cardiovascular_phenotype|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 2,
    "not_specified|not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype": 1,
    "RASopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_4|RASopathy|not_provided|Fibromatosis|_gingival|_1": 1,
    "not_provided|RASopathy|not_specified|Cardiovascular_phenotype": 1,
    "Fibromatosis|_gingival|_1|Inborn_genetic_diseases": 1,
    "SOS1-related_disorder|not_provided|RASopathy|Noonan_syndrome_4|Noonan_syndrome_3": 1,
    "not_specified|SOS1-related_disorder": 1,
    "Noonan_syndrome_4|not_provided|Noonan_syndrome|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome": 2,
    "not_specified|not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 2,
    "RASopathy|not_provided|not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "Noonan_syndrome_4|not_provided|RASopathy|not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Fibromatosis|_gingival|_1|not_specified": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy": 1,
    "RASopathy|Noonan_syndrome_4|Cardiovascular_phenotype": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Joubert_syndrome_3|not_provided|Cardiovascular_phenotype|Noonan_syndrome_4|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Fibromatosis|_gingival|_1|not_specified": 1,
    "not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 2,
    "RASopathy|Noonan_syndrome|Noonan_syndrome_4|not_provided|Fibromatosis|_gingival|_1": 1,
    "not_specified|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "not_provided|RASopathy|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Noonan_syndrome|not_specified|Gingival_fibromatosis|RASopathy|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|Cardiovascular_phenotype|RASopathy": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|Cardiovascular_phenotype": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|RASopathy|Noonan_syndrome_4": 1,
    "not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|SOS1-related_disorder|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy": 1,
    "SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy": 2,
    "RASopathy|not_provided|Noonan_syndrome|not_specified": 1,
    "Noonan_syndrome_1|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 2,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|not_specified": 1,
    "RASopathy|not_specified|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|RASopathy|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "SOS1-related_disorder|not_provided": 2,
    "RASopathy|SOS1-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 2,
    "Obesity|Cardiovascular_phenotype": 1,
    "not_provided|Noonan_syndrome_4|RASopathy": 1,
    "SOS1-related_disorder|RASopathy|not_provided": 1,
    "not_specified|Noonan_syndrome_1|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy": 1,
    "RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified|Cardiovascular_phenotype": 1,
    "SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Noonan_syndrome_1|Cardiovascular_phenotype|not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "not_specified|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|RASopathy": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|Cardiovascular_phenotype": 3,
    "RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 2,
    "not_specified|Noonan_syndrome_4|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided|RASopathy|Noonan_syndrome|See_cases": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|Noonan_syndrome|Noonan_syndrome_1": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome": 1,
    "Noonan_syndrome|not_provided|SOS1-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_1|Noonan_syndrome_4|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Abnormal_aortic_valve_morphology": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|Noonan_syndrome_3|not_provided|Noonan_syndrome|Noonan_syndrome_1|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|Noonan_syndrome": 1,
    "RASopathy|SOS1-related_disorder|Cardiovascular_phenotype|Noonan_syndrome|Noonan_syndrome_4|Noonan_syndrome_1|not_provided": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|not_specified": 5,
    "not_provided|Noonan_syndrome|Noonan_syndrome_4|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|Noonan_syndrome|Noonan_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|See_cases|not_specified|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_4|RASopathy|Fibromatosis|_gingival|_1|not_provided": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 3,
    "not_specified|Cardiovascular_phenotype|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Cardiovascular_phenotype|not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 2,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Noonan_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|not_specified|Noonan_syndrome_1": 1,
    "not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|SOS1-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "Fibromatosis|_gingival|_1|not_specified|Noonan_syndrome_4|Cardiovascular_phenotype": 1,
    "See_cases|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome_4|not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|not_specified": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|RASopathy": 2,
    "RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype": 2,
    "RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided": 1,
    "Atrial_septal_defect|Cafe_au_lait_spots|_multiple": 1,
    "Noonan_syndrome|not_provided|Noonan_syndrome_4|RASopathy": 1,
    "Noonan_syndrome_4|not_provided|Noonan_syndrome|RASopathy|Fibromatosis|_gingival|_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Male_subfertility|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|not_provided|Noonan_syndrome": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|Pulmonic_stenosis|Ptosis|Abnormal_sternum_morphology|Short_stature|Fetal_cystic_hygroma|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_1": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_4|Noonan_syndrome_1|Noonan_syndrome": 1,
    "Noonan_syndrome|RASopathy|not_provided|Noonan_syndrome_4": 1,
    "not_provided|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Cardiovascular_phenotype|RASopathy|not_specified": 17,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|not_provided|RASopathy": 3,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|RASopathy": 1,
    "Noonan_syndrome|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified|not_provided": 1,
    "not_provided|Noonan_syndrome_4|RASopathy|not_specified|Fibromatosis|_gingival|_1": 2,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|not_specified|RASopathy": 2,
    "SOS1-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 2,
    "Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_4": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_4|not_provided|Fibromatosis|_gingival|_1|SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy": 1,
    "SOS1-related_disorder|not_specified|RASopathy|Cardiovascular_phenotype": 1,
    "SOS1-related_disorder|not_provided|RASopathy|Intellectual_disability": 1,
    "not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy": 1,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|RASopathy|Cardiovascular_phenotype|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_4|not_provided|Noonan_syndrome": 1,
    "Fibromatosis|_gingival|_1|Cardiovascular_phenotype|not_specified|RASopathy|Noonan_syndrome_4": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Cardiovascular_phenotype|Fibromatosis|_gingival|_1|RASopathy|Noonan_syndrome_4": 1,
    "not_specified|RASopathy|Fibromatosis|_gingival|_1|not_provided|Noonan_syndrome_4|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|Cardiovascular_phenotype": 3,
    "RASopathy|not_specified|Cardiovascular_phenotype|not_provided": 3,
    "not_specified|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "SOS1-related_disorder|RASopathy": 3,
    "Noonan_syndrome|RASopathy|SOS1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_1|Noonan_syndrome_4": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome|RASopathy|Noonan_syndrome_1|Noonan_syndrome_4": 1,
    "Noonan_syndrome_4|Cardiovascular_phenotype|not_provided|RASopathy": 2,
    "not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|Noonan_syndrome_1": 1,
    "not_specified|not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Noonan_syndrome_4|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "RASopathy|not_specified|Cardiovascular_phenotype|SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan_syndrome": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy": 1,
    "not_provided|Noonan_syndrome_4|Noonan_syndrome|not_specified": 1,
    "not_provided|Noonan_syndrome_4|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|RASopathy|Noonan_syndrome|SOS1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Fibromatosis|_gingival|_1|RASopathy|not_provided|not_specified|Noonan_syndrome_4": 1,
    "not_provided|Cardiovascular_phenotype|not_specified": 70,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Cardiovascular_phenotype|SOS1-related_disorder|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Noonan_syndrome_4|RASopathy|Fibromatosis|_gingival|_1|Cardiovascular_phenotype|not_specified": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|not_provided|RASopathy|Noonan_syndrome|Primary_dilated_cardiomyopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "RASopathy|Inborn_genetic_diseases|Noonan_syndrome_4|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan_syndrome": 1,
    "not_specified|Noonan_syndrome_4": 1,
    "Fibromatosis|_gingival|_1": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy|SOS1-related_disorder": 1,
    "SOS1-related_disorder|not_specified|RASopathy|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "Neonatal_hypotonia|not_provided|Cardiovascular_phenotype|Noonan_syndrome|Noonan_syndrome_4|SOS1-related_disorder|RASopathy|not_specified": 1,
    "Cardiovascular_phenotype|RASopathy|Noonan_syndrome_4": 1,
    "SOS1-related_disorder|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_4|not_specified|not_provided|RASopathy": 1,
    "46|XY_partial_gonadal_dysgenesis": 2,
    "Noonan_syndrome_4|not_specified|Noonan_syndrome|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|RASopathy": 1,
    "RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|Cardiovascular_phenotype": 1,
    "RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_4": 1,
    "Noonan_syndrome_4|RASopathy|not_provided": 1,
    "See_cases|Noonan_syndrome_4|not_specified|Fibromatosis|_gingival|_1": 1,
    "RASopathy|not_provided|Noonan_syndrome|Cardiovascular_phenotype": 2,
    "Fibromatosis|_gingival|_1|Noonan_syndrome_4|Noonan_syndrome|RASopathy": 1,
    "not_provided|Noonan_syndrome|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_1|SOS1-related_disorder|Noonan_syndrome_4|RASopathy|not_specified|Ventricular_tachycardia": 1,
    "RASopathy|not_provided|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified": 1,
    "RASopathy|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4": 1,
    "not_specified|RASopathy|Noonan_syndrome_4|Fibromatosis|_gingival|_1": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_4|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|RASopathy": 19,
    "Cardiovascular_phenotype|not_provided|Fibromatosis|_gingival|_1|Noonan_syndrome_4|RASopathy": 1,
    "SOS1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_provided|RASopathy": 1,
    "Noonan_syndrome_4|not_specified|SOS1-related_disorder|RASopathy|Fibromatosis|_gingival|_1|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_specified|Noonan_syndrome_4|Fibromatosis|_gingival|_1|RASopathy": 1,
    "Noonan_syndrome_4|Fibromatosis|_gingival|_1|not_specified|SOS1-related_disorder|RASopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy": 1,
    "Noonan_syndrome_4|RASopathy|Fibromatosis|_gingival|_1|not_provided|Noonan_syndrome": 1,
    "RASopathy|SOS1-related_disorder": 1,
    "RASopathy|SOS1-related_disorder|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|RASopathy": 1,
    "Rhizomelic_limb_shortening_with_dysmorphic_features": 5,
    "not_provided|Rhizomelic_limb_shortening_with_dysmorphic_features": 5,
    "not_provided|PKDCC-related_disorder|Inborn_genetic_diseases|Skeletal_dysplasia": 1,
    "Rhizomelic_limb_shortening_with_dysmorphic_features|not_provided": 1,
    "Rhizomelic_limb_shortening_with_dysmorphic_features|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Rhizomelic_limb_shortening_with_dysmorphic_features": 1,
    "PKDCC-related_disorder": 1,
    "PKDCC-related_disorder|not_provided": 1,
    "Abnormality_of_the_skeletal_system|not_provided|Rhizomelic_limb_shortening_with_dysmorphic_features": 1,
    "Inborn_genetic_diseases|PKDCC-related_disorder|not_provided": 1,
    "PKDCC-related_disorder|Inborn_genetic_diseases": 1,
    "Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4": 1,
    "EML4-related_disorder": 2,
    "HAAO-related_disorder|not_provided": 1,
    "HAAO-related_disorder": 6,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_1|not_provided": 5,
    "Congenital_NAD_deficiency_disorder|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_1": 4,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_1": 6,
    "Congenital_NAD_deficiency_disorder|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_1|not_provided": 2,
    "Congenital_NAD_deficiency_disorder|not_provided|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_1": 1,
    "ZFP36L2-related_disorder": 12,
    "Oocyte_maturation_defect_13": 2,
    "THADA-related_disorder": 33,
    "not_provided|THADA-related_disorder": 5,
    "not_specified|THADA-related_disorder": 2,
    "THADA-related_disorder|Meniere_disease": 1,
    "Abnormality_of_neuronal_migration": 79,
    "not_provided|Short-rib_thoracic_dysplasia_15_with_polydactyly": 2,
    "Short-rib_thoracic_dysplasia_15_with_polydactyly": 8,
    "DYNC2LI1-related_disorder|not_provided|Short-rib_thoracic_dysplasia_15_with_polydactyly": 1,
    "not_provided|Inborn_genetic_diseases|DYNC2LI1-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_15_with_polydactyly|Asphyxiating_thoracic_dystrophy_1|not_provided": 1,
    "Short-rib_thoracic_dysplasia_15_with_polydactyly|not_provided|Asphyxiating_thoracic_dystrophy_1": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_15_with_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 463,
    "Short-rib_thoracic_dysplasia_15_with_polydactyly|not_provided": 3,
    "DYNC2LI1-related_disorder|not_provided": 3,
    "not_provided|DYNC2LI1-related_disorder": 3,
    "not_provided|Short-rib_thoracic_dysplasia_15_with_polydactyly|Asphyxiating_thoracic_dystrophy_1": 1,
    "Asphyxiating_thoracic_dystrophy_1|Short-rib_thoracic_dysplasia_15_with_polydactyly": 2,
    "DYNC2LI1-related_disorder": 1,
    "not_provided|Sitosterolemia_1": 20,
    "Sitosterolemia_1": 71,
    "Sitosterolemia": 163,
    "Sitosterolemia|Sitosterolemia_2|Sitosterolemia_1|not_provided": 1,
    "Sitosterolemia_2|Sitosterolemia|not_provided": 1,
    "Cardiovascular_phenotype|Sitosterolemia": 34,
    "not_provided|Sitosterolemia|Cardiovascular_phenotype|Thrombocytopenia|ABCG5-related_disorder|Sitosterolemia_1|Sitosterolemia_2": 1,
    "Cardiovascular_phenotype|Sitosterolemia_2|Sitosterolemia_1|not_specified|not_provided|Sitosterolemia": 1,
    "Sitosterolemia_2|Sitosterolemia|Cardiovascular_phenotype": 2,
    "Sitosterolemia|Cardiovascular_phenotype": 13,
    "Sitosterolemia_2|Cardiovascular_phenotype": 9,
    "Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "not_provided|Sitosterolemia|Cardiovascular_phenotype|Sitosterolemia_1|not_specified": 1,
    "Sitosterolemia|Sitosterolemia_2": 1,
    "not_provided|Sitosterolemia": 7,
    "not_specified|not_provided|Sitosterolemia": 2,
    "Cardiovascular_phenotype|Sitosterolemia_2": 10,
    "Sitosterolemia|not_specified|Cardiovascular_phenotype": 1,
    "ABCG5-related_disorder|Sitosterolemia_1|Sitosterolemia_2|not_provided|not_specified|Sitosterolemia|Cardiovascular_phenotype": 1,
    "Sitosterolemia|not_provided|ABCG5-related_disorder|Cardiovascular_phenotype|Sitosterolemia_2": 1,
    "Sitosterolemia_2": 35,
    "ABCG5-related_disorder": 12,
    "Cardiovascular_phenotype|not_provided|Sitosterolemia": 2,
    "Sitosterolemia_1|Sitosterolemia_2|not_provided|Sitosterolemia|not_specified": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|Sitosterolemia": 1,
    "not_provided|Sitosterolemia|not_specified|ABCG5-related_disorder|Sitosterolemia_1|Cardiovascular_phenotype": 1,
    "not_provided|Sitosterolemia_2": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Sitosterolemia_1|Sitosterolemia": 1,
    "Sitosterolemia_2|not_provided|Sitosterolemia": 3,
    "not_provided|Sitosterolemia|Cardiovascular_phenotype|ABCG5-related_disorder|Sitosterolemia_2|not_specified": 1,
    "not_provided|Sitosterolemia|ABCG5-related_disorder": 3,
    "Sitosterolemia|ABCG5-related_disorder": 4,
    "ABCG5-related_disorder|not_provided|Sitosterolemia": 1,
    "ABCG5-related_disorder|Sitosterolemia_1|Sitosterolemia_2|Sitosterolemia|Cardiovascular_phenotype|not_provided": 1,
    "ABCG5-related_disorder|not_provided|Cardiovascular_phenotype|Sitosterolemia": 1,
    "Sitosterolemia|Sitosterolemia_2|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Sitosterolemia|not_provided|Sitosterolemia_1|not_specified": 1,
    "ABCG5-related_disorder|Sitosterolemia_2|Sitosterolemia": 2,
    "Cardiovascular_phenotype|Sitosterolemia_2|Sitosterolemia": 4,
    "not_specified|Sitosterolemia|Cardiovascular_phenotype": 1,
    "not_provided|Sitosterolemia_2|Short-rib_thoracic_dysplasia_15_with_polydactyly": 1,
    "Cardiovascular_phenotype|Sitosterolemia_2|Sitosterolemia_1|Short-rib_thoracic_dysplasia_15_with_polydactyly|not_provided|Sitosterolemia": 1,
    "Cardiovascular_phenotype|Sitosterolemia|not_specified": 1,
    "Sitosterolemia|not_provided|Cardiovascular_phenotype": 1,
    "Sitosterolemia|Cardiovascular_phenotype|ABCG5-related_disorder": 1,
    "Sitosterolemia|not_provided": 4,
    "not_provided|Sitosterolemia|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|Sitosterolemia": 1,
    "Sitosterolemia_1|Sitosterolemia_2|Cardiovascular_phenotype|Sitosterolemia": 1,
    "not_specified|Sitosterolemia|not_provided": 1,
    "not_specified|ABCG5-related_disorder|Sitosterolemia_1|Cardiovascular_phenotype|not_provided|Sitosterolemia": 1,
    "Cardiovascular_phenotype|not_specified|Sitosterolemia_1|not_provided|Sitosterolemia": 1,
    "Sitosterolemia|Sitosterolemia_2|ABCG5-related_disorder": 1,
    "Sitosterolemia_2|Sitosterolemia": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|not_provided|Sitosterolemia_2": 2,
    "Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype": 2,
    "Sitosterolemia|not_provided|Cardiovascular_phenotype|Sitosterolemia_2|not_specified": 1,
    "Cardiovascular_phenotype|Sitosterolemia_2|ABCG5-related_disorder|not_provided|Sitosterolemia": 1,
    "ABCG5-related_disorder|Sitosterolemia_2|Sitosterolemia|Cardiovascular_phenotype|not_provided|Sitosterolemia_1": 1,
    "Sitosterolemia_1|Sitosterolemia": 1,
    "Sitosterolemia|not_specified": 3,
    "ABCG5-related_disorder|not_specified|Sitosterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Sitosterolemia|Sitosterolemia_2": 2,
    "Cardiovascular_phenotype|Sitosterolemia|not_provided": 2,
    "Sitosterolemia|not_provided|Cardiovascular_phenotype|ABCG5-related_disorder": 2,
    "ABCG5-related_disorder|Sitosterolemia": 2,
    "Cardiovascular_phenotype|Sitosterolemia_2|Sitosterolemia_1|Sitosterolemia": 1,
    "ABCG5-related_disorder|Sitosterolemia|not_specified": 1,
    "Sitosterolemia_1|Sitosterolemia_2|Sitosterolemia|Cardiovascular_phenotype": 1,
    "not_specified|ABCG5-related_disorder|not_provided|Cardiovascular_phenotype|Sitosterolemia": 1,
    "not_provided|Sitosterolemia|Cardiovascular_phenotype|ABCG5-related_disorder": 1,
    "Cardiovascular_phenotype|Sitosterolemia_1|Sitosterolemia": 1,
    "ABCG5-related_disorder|Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype|not_provided": 2,
    "Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype|not_specified": 1,
    "Sitosterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Thrombocytopenia": 95,
    "not_provided|Sitosterolemia|Sitosterolemia_1|not_specified": 1,
    "Sitosterolemia|ABCG5-related_disorder|not_provided|Cardiovascular_phenotype|Sitosterolemia_2": 1,
    "Sitosterolemia_2|ABCG5-related_disorder": 1,
    "Sitosterolemia_2|not_provided|Sitosterolemia|Cardiovascular_phenotype": 1,
    "Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Thrombocytopenia|Abnormal_bleeding|not_provided": 3,
    "Sitosterolemia|Cardiovascular_phenotype|Sitosterolemia_2": 3,
    "not_provided|Sitosterolemia|Cardiovascular_phenotype|ABCG5-related_disorder|not_specified": 1,
    "ABCG5-related_disorder|Cardiovascular_phenotype|Sitosterolemia": 3,
    "not_provided|Sitosterolemia|Sitosterolemia_2": 1,
    "Sitosterolemia_2|not_provided": 2,
    "ABCG5-related_disorder|Sitosterolemia_1|Sitosterolemia_2|not_provided|Sitosterolemia|Cardiovascular_phenotype|not_specified": 1,
    "Sitosterolemia_2|Short-rib_thoracic_dysplasia_15_with_polydactyly": 1,
    "Cardiovascular_phenotype|Sitosterolemia_1|Sitosterolemia|not_provided": 1,
    "Cardiovascular_phenotype|Sitosterolemia_1": 16,
    "Cardiovascular_phenotype|Sitosterolemia_2|Sitosterolemia_1": 1,
    "Sitosterolemia|not_provided|ABCG5-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|ABCG5-related_disorder|Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype": 1,
    "Sitosterolemia_2|Sitosterolemia|ABCG5-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Sitosterolemia_2|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Sitosterolemia_2|ABCG5-related_disorder|not_provided|Sitosterolemia": 1,
    "Sitosterolemia|ABCG5-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Sitosterolemia_2|ABCG5-related_disorder|Sitosterolemia|Cardiovascular_phenotype": 1,
    "Sitosterolemia_1|Hyperuricemic_nephropathy|_familial_juvenile_type_4|Cardiovascular_phenotype|ABCG5-related_disorder|not_specified|not_provided|Sitosterolemia": 1,
    "Sitosterolemia_1|Sitosterolemia_2|not_provided": 1,
    "not_specified|Sitosterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|not_provided|Sitosterolemia": 1,
    "ABCG5-related_disorder|Sitosterolemia_2|not_provided|Sitosterolemia": 1,
    "not_specified|Sitosterolemia_1|Sitosterolemia_2|Cardiovascular_phenotype|not_provided|Sitosterolemia": 1,
    "not_provided|Sitosterolemia_2|Sitosterolemia_1|Sitosterolemia|Cardiovascular_phenotype": 1,
    "ABCG5-related_disorder|Sitosterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Sitosterolemia|ABCG5-related_disorder|Sitosterolemia_1|not_specified|not_provided": 1,
    "Sitosterolemia_2|Sitosterolemia_1|ABCG5-related_disorder|Cardiovascular_phenotype|not_specified|Sitosterolemia|not_provided": 1,
    "Sitosterolemia_2|Sitosterolemia_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Sitosterolemia_2|Sitosterolemia|Cardiovascular_phenotype": 1,
    "not_specified|Sitosterolemia|Sitosterolemia_2|not_provided|Cardiovascular_phenotype": 1,
    "ABCG5-related_disorder|not_provided|not_specified|Sitosterolemia|Cardiovascular_phenotype": 1,
    "Sitosterolemia_2|Cardiovascular_phenotype|not_provided|Sitosterolemia": 1,
    "ABCG5-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|ABCG5-related_disorder|Sitosterolemia_1|Cardiovascular_phenotype|not_provided|Thrombocytopenia|Sitosterolemia": 1,
    "Sitosterolemia_2|Sitosterolemia|Sitosterolemia_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Sitosterolemia|Abnormal_circulating_lipid_concentration|Hypercholesterolemia": 1,
    "Sitosterolemia|Sitosterolemia_2|Cardiovascular_phenotype|not_specified|ABCG5-related_disorder": 1,
    "ABCG5-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Sitosterolemia_1|not_specified|Sitosterolemia|not_provided": 1,
    "Sitosterolemia_1|not_provided|Sitosterolemia": 1,
    "ABCG8-related_disorder": 18,
    "Sitosterolemia_1|not_provided|not_specified|Sitosterolemia": 1,
    "Sitosterolemia_1|not_specified|not_provided|Sitosterolemia": 1,
    "Early-onset_coronary_artery_disease|not_provided": 1,
    "ABCG8-related_disorder|Cardiovascular_phenotype|not_provided": 6,
    "not_provided|Cardiovascular_phenotype|Sitosterolemia_1": 4,
    "Sitosterolemia_1|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "Gallstones|Cardiovascular_phenotype|Sitosterolemia_2|ABCG8-related_disorder|Sitosterolemia_1|not_specified|not_provided|Gallbladder_disease_4|Sitosterolemia": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|ABCG8-related_disorder|not_provided": 4,
    "not_provided|Sitosterolemia_1|not_specified": 1,
    "Sitosterolemia_1|ABCG8-related_disorder|not_provided": 1,
    "Sitosterolemia_1|not_provided": 19,
    "Sitosterolemia_1|Cardiovascular_phenotype|ABCG8-related_disorder|not_specified|not_provided": 1,
    "Gallbladder_disease_4|Sitosterolemia_1|not_specified|not_provided|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Sitosterolemia_1|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Sitosterolemia_1|not_provided": 2,
    "not_specified|not_provided|Sitosterolemia_1|Cardiovascular_phenotype": 2,
    "Sitosterolemia_1|not_specified|not_provided": 2,
    "Sitosterolemia_1|not_provided|Cardiovascular_phenotype": 7,
    "Cardiovascular_phenotype|not_provided|Sitosterolemia_1": 6,
    "Sitosterolemia_1|not_specified|Cardiovascular_phenotype|not_provided": 3,
    "not_specified|not_provided|Cardiovascular_phenotype": 72,
    "not_provided|not_specified|Sitosterolemia_1|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Sitosterolemia_1|Cardiovascular_phenotype": 5,
    "ABCG8-related_disorder|not_provided": 7,
    "not_provided|Cardiovascular_phenotype|ABCG8-related_disorder": 3,
    "ABCG8-related_disorder|Cardiovascular_phenotype": 3,
    "not_provided|ABCG8-related_disorder": 3,
    "not_provided|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Gallbladder_disease_4|Sitosterolemia_1": 1,
    "Cardiovascular_phenotype|ABCG8-related_disorder|not_provided": 4,
    "not_specified|ABCG8-related_disorder|Cardiovascular_phenotype|not_provided|Sitosterolemia_1": 1,
    "Gallbladder_disease_4|Sitosterolemia_1|Cardiovascular_phenotype|not_provided|ABCG8-related_disorder|not_specified": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|not_provided": 5,
    "Premature_coronary_artery_atherosclerosis|Cardiovascular_phenotype": 1,
    "ABCG8-related_disorder|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|ABCG8-related_disorder|Sitosterolemia_1": 1,
    "not_specified|Sitosterolemia_1|not_provided": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Sitosterolemia_1|not_provided|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Sitosterolemia_1|Gallbladder_disease_4": 1,
    "Cardiovascular_phenotype|ABCG8-related_disorder": 6,
    "Sitosterolemia_1|Sitosterolemia|ABCG8-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|ABCG8-related_disorder|Sitosterolemia_1|Gallbladder_disease_4|not_provided|Sitosterolemia": 1,
    "ABCG8-related_disorder|not_specified|Sitosterolemia_1|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|ABCG8-related_disorder": 1,
    "Cardiovascular_phenotype|Sitosterolemia_1|ABCG8-related_disorder": 1,
    "ABCG8-related_disorder|Sitosterolemia_1|not_specified|not_provided": 1,
    "Sitosterolemia_1|ABCG8-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "ABCG8-related_disorder|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|ABCG8-related_disorder|Sitosterolemia_1|not_specified|not_provided": 1,
    "not_provided|Early-onset_coronary_artery_disease": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|not_specified": 2,
    "Sitosterolemia|Sitosterolemia_1|Gallbladder_disease_4|ABCG8-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|ABCG8-related_disorder|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Sitosterolemia_1": 1,
    "Sitosterolemia_1|not_specified|Cardiovascular_phenotype|ABCG8-related_disorder|not_provided": 1,
    "not_specified|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "Sitosterolemia_1|ABCG8-related_disorder|not_specified|not_provided|Cardiovascular_phenotype|Sitosterolemia|Gallbladder_disease_4": 1,
    "Cardiovascular_phenotype|ABCG8-related_disorder|not_provided|not_specified|Sitosterolemia_1": 1,
    "Cardiovascular_phenotype|ABCG8-related_disorder|Sitosterolemia_1|Gallbladder_disease_4|Sitosterolemia|not_provided": 1,
    "Sitosterolemia_1|Gallbladder_disease_4|not_provided": 1,
    "not_specified|ABCG8-related_disorder|Sitosterolemia_1|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|ABCG8-related_disorder|not_specified": 1,
    "Sitosterolemia|Sitosterolemia_1|ABCG8-related_disorder|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Sitosterolemia_1|not_specified|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "ABCG8-related_disorder|Sitosterolemia_1|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Sitosterolemia_1": 2,
    "ABCG8-related_disorder|Sitosterolemia_1|Cardiovascular_phenotype|not_provided": 2,
    "ABCG8-related_disorder|Cardiovascular_phenotype|not_specified|Sitosterolemia_1|not_provided": 1,
    "Sitosterolemia_1|Gallbladder_disease_4|not_specified|not_provided": 1,
    "Sitosterolemia|not_specified|not_provided": 1,
    "not_provided|not_specified|Sitosterolemia_1": 2,
    "ABCG8-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|ABCG8-related_disorder|Gallbladder_disease_4|not_provided|Sitosterolemia": 1,
    "Gallbladder_disease_4|Sitosterolemia_1|not_provided": 1,
    "not_specified|not_provided|Sitosterolemia_1|Cardiovascular_phenotype|ABCG8-related_disorder": 1,
    "not_provided|not_specified|ABCG8-related_disorder": 1,
    "Gallbladder_disease_4|Sitosterolemia_1|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Sitosterolemia_1|not_specified|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Sitosterolemia_1|ABCG8-related_disorder": 1,
    "not_provided|Sitosterolemia|Sitosterolemia_1|ABCG8-related_disorder": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|not_provided|Gallbladder_disease_4": 1,
    "ABCG8-related_disorder|Sitosterolemia_1|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Sitosterolemia_1|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "ABCG8-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|ABCG8-related_disorder": 1,
    "Sitosterolemia_1|not_specified|ABCG8-related_disorder|Gallbladder_disease_4|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Sitosterolemia_1": 1,
    "Sitosterolemia|Sitosterolemia_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Sitosterolemia_1|Sitosterolemia|ABCG8-related_disorder|not_provided|Cardiovascular_phenotype|Early-onset_coronary_artery_disease": 1,
    "not_provided|Sitosterolemia_1|Cardiovascular_phenotype|not_specified": 1,
    "ABCG8-related_disorder|Sitosterolemia_1|not_provided": 1,
    "Gallbladder_disease_4|Sitosterolemia_1|not_provided|ABCG8-related_disorder|Cardiovascular_phenotype": 1,
    "Sitosterolemia_1|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Sitosterolemia_1|ABCG8-related_disorder": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Sitosterolemia_1": 1,
    "Sitosterolemia_1|not_provided|ABCG8-related_disorder": 1,
    "ABCG8-related_disorder|Cardiovascular_phenotype|Sitosterolemia_1|not_provided|Abnormal_bleeding|Thrombocytopenia": 1,
    "Abnormal_circulating_lipid_concentration": 6,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 358,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided": 80,
    "not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 95,
    "not_specified|not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 13,
    "LRPPRC-related_disorder|not_provided": 5,
    "not_provided|not_specified|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 2,
    "Inborn_genetic_diseases|LRPPRC-related_disorder|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 1,
    "LRPPRC-related_disorder|not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 7,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|Inborn_genetic_diseases|not_provided": 3,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|LRPPRC-related_disorder|not_provided": 4,
    "not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|LRPPRC-related_disorder": 1,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided|Inborn_genetic_diseases": 3,
    "LRPPRC-related_disorder": 5,
    "Inborn_genetic_diseases|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 11,
    "not_specified|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 1,
    "not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided": 1,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_specified": 2,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|Inborn_genetic_diseases": 5,
    "not_provided|LRPPRC-related_disorder": 8,
    "not_specified|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided": 6,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 5,
    "LRPPRC-related_disorder|not_specified|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_5|_French-Canadian|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 4,
    "Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided|not_specified": 2,
    "LRPPRC-related_disorder|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided": 1,
    "Leigh_syndrome|not_specified|not_provided": 6,
    "LRPPRC-related_disorder|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_provided": 2,
    "not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type|not_specified": 1,
    "not_specified|not_provided|LRPPRC-related_disorder": 1,
    "not_specified|LRPPRC-related_disorder|not_provided|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 1,
    "LRPPRC-related_disorder|not_specified|not_provided": 1,
    "LRPPRC-related_disorder|Inborn_genetic_diseases|not_provided|Leigh_syndrome|Congenital_lactic_acidosis|_Saguenay-Lac-Saint-Jean_type": 1,
    "Inborn_genetic_diseases|Cystinuria": 2,
    "not_provided|not_specified|Cystinuria": 1,
    "Cystinuria|Inborn_genetic_diseases": 2,
    "Cystinuria|not_provided": 54,
    "SLC3A1-related_disorder": 6,
    "SLC3A1-related_disorder|Cystinuria|not_provided": 1,
    "not_provided|Cystinuria": 47,
    "Cystinuria|SLC3A1-related_disorder": 3,
    "Nephrolithiasis|Nephrocalcinosis|not_provided|Cystinuria": 1,
    "not_provided|SLC3A1-related_disorder|Cystinuria": 2,
    "Cystinuria|not_provided|SLC3A1-related_disorder": 1,
    "Cystinuria|SLC3A1-related_disorder|Autism_spectrum_disorder|not_provided": 1,
    "Cystine_urolithiasis|not_specified": 2,
    "SLC3A1-related_disorder|Cystinuria": 6,
    "not_provided|Cystinuria|not_specified": 2,
    "Cystine_urolithiasis": 11,
    "Cystine_urolithiasis|Cystinuria|SLC3A1-related_disorder": 1,
    "Cystinuria|Cystine_urolithiasis": 3,
    "not_specified|Cystinuria|not_provided": 1,
    "Cystine_urolithiasis|Cystinuria": 2,
    "Cystinuria|not_specified": 1,
    "not_specified|not_provided|Cystinuria": 2,
    "not_provided|Cystinuria|SLC3A1-related_disorder": 1,
    "SLC3A1-related_disorder|Kidney_disorder|Inborn_genetic_diseases|not_provided|Cystinuria|See_cases": 1,
    "Inborn_genetic_diseases|Cystinuria|not_provided": 1,
    "Cystine_urolithiasis|SLC3A1-related_disorder|Cystinuria": 1,
    "Myasthenic_syndrome|_congenital|_22": 516,
    "not_specified|Myasthenic_syndrome|_congenital|_22|not_provided": 1,
    "Myasthenic_syndrome|_congenital|_22|not_provided": 10,
    "Myasthenic_syndrome|_congenital|_22|Inborn_genetic_diseases|not_provided": 1,
    "Myasthenic_syndrome|_congenital|_22|Inborn_genetic_diseases": 35,
    "not_provided|Inborn_genetic_diseases|Myasthenic_syndrome|_congenital|_22": 1,
    "Inborn_genetic_diseases|Myasthenic_syndrome|_congenital|_22": 24,
    "not_provided|Myasthenic_syndrome|_congenital|_22": 16,
    "not_provided|Myasthenic_syndrome|_congenital|_22|Intellectual_disability": 1,
    "PREPL-related_disorder": 6,
    "not_specified|Inborn_genetic_diseases|Myasthenic_syndrome|_congenital|_22": 1,
    "Inborn_genetic_diseases|Myasthenic_syndrome|_congenital|_22|not_provided": 3,
    "PREPL-related_disorder|Myasthenic_syndrome|_congenital|_22|not_provided|not_specified": 1,
    "PREPL-related_disorder|Myasthenic_syndrome|_congenital|_22": 4,
    "Myasthenic_syndrome|_congenital|_22|PREPL-related_disorder|not_provided": 2,
    "not_provided|Myasthenic_syndrome|_congenital|_22|Inborn_genetic_diseases": 1,
    "Myasthenic_syndrome|_congenital|_22|PREPL-related_disorder": 2,
    "PREPL-related_disorder|Myasthenic_syndrome|_congenital|_22|not_provided": 2,
    "Inborn_genetic_diseases|Myasthenic_syndrome|_congenital|_22|PREPL-related_disorder": 1,
    "not_specified|Myasthenic_syndrome|_congenital|_22": 2,
    "not_provided|Myasthenic_syndrome|_congenital|_22|PREPL-related_disorder": 1,
    "Myasthenic_syndrome|_congenital|_22|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|PREPL-related_disorder|Myasthenic_syndrome|_congenital|_22": 1,
    "Myasthenic_syndrome|_congenital|_22|See_cases": 1,
    "Myasthenic_syndrome|_congenital|_22|Inborn_genetic_diseases|PREPL-related_disorder": 1,
    "Holoprosencephaly_2": 95,
    "not_provided|Holoprosencephaly_2": 10,
    "Holoprosencephaly_2|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|Holoprosencephaly_2": 2,
    "SIX3-related_disorder|Holoprosencephaly_2": 1,
    "SIX3-related_disorder": 6,
    "Holoprosencephaly_2|not_provided": 6,
    "Schizencephaly|Holoprosencephaly_2": 3,
    "not_provided|Inborn_genetic_diseases|Holoprosencephaly_2": 1,
    "SIX3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Schizencephaly|Solitary_median_maxillary_central_incisor_syndrome|Holoprosencephaly_2": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_2": 3,
    "Holoprosencephaly_2|Schizencephaly|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Holoprosencephaly_2": 1,
    "Holoprosencephaly_2|Schizencephaly|not_specified|not_provided": 1,
    "Holoprosencephaly_2|SIX3-related_disorder": 4,
    "Holoprosencephaly_2|Schizencephaly|Intellectual_disability": 1,
    "Schizencephaly": 11,
    "not_specified|Holoprosencephaly_2|not_provided": 1,
    "Holoprosencephaly_2|not_specified": 1,
    "not_specified|Holoprosencephaly_2": 1,
    "SIX3-related_disorder|not_provided|Holoprosencephaly_2": 1,
    "Schizencephaly|not_specified": 1,
    "Holoprosencephaly_2|not_specified|not_provided": 1,
    "Schizencephaly|Holoprosencephaly_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_2": 1,
    "not_provided|not_specified|Holoprosencephaly_2": 1,
    "not_provided|Holoprosencephaly_2|Inborn_genetic_diseases": 1,
    "not_provided|Holoprosencephaly_2|not_specified": 2,
    "SIX3-related_disorder|not_provided": 1,
    "not_provided|Holoprosencephaly_2|SIX3-related_disorder|not_specified": 1,
    "SIX2-related_disorder": 7,
    "SIX2-related_disorder|not_specified": 1,
    "SIX2-related_disorder|not_provided": 3,
    "SIX2-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "SIX2-related_disorder|not_specified|not_provided": 1,
    "PRKCE-associated_disorder": 1,
    "not_provided|Erythrocytosis|_familial|_4": 15,
    "Erythrocytosis|_familial|_4": 80,
    "not_provided|Erythrocytosis|_familial|_4|Inborn_genetic_diseases": 3,
    "Erythrocytosis|_familial|_4|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Erythrocytosis|_familial|_4": 3,
    "Inborn_genetic_diseases|not_provided|Erythrocytosis|_familial|_4": 9,
    "EPAS1-related_disorder": 3,
    "Erythrocytosis|_familial|_4|not_provided": 12,
    "EPAS1-related_disorder|Familial_erythrocytosis": 1,
    "Erythrocytosis|_familial|_4|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Erythrocytosis|_familial|_4|not_provided": 3,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3": 7,
    "Inborn_genetic_diseases|Erythrocytosis|_familial|_4": 13,
    "not_provided|EPAS1-related_disorder": 1,
    "not_specified|not_provided|Erythrocytosis|_familial|_4": 2,
    "EPAS1-related_disorder|Erythrocytosis|_familial|_4|not_provided": 1,
    "Erythrocytosis|_familial|_4|not_provided|Inborn_genetic_diseases": 1,
    "EPAS1-related_disorder|not_provided|sorafenib_response_-_Toxicity|Erythrocytosis|_familial|_4": 1,
    "Erythrocytosis|_familial|_4|not_specified|not_provided": 1,
    "EPAS1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Erythrocytosis|_familial|_4|Inborn_genetic_diseases": 1,
    "Teratoma|Inborn_genetic_diseases": 2,
    "EPAS1-related_disorder|not_provided|Erythrocytosis|_familial|_4": 3,
    "Familial_erythrocytosis|not_provided|Erythrocytosis|_familial|_4": 1,
    "EPAS1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|EPAS1-related_disorder|Erythrocytosis|_familial|_4": 1,
    "Onychodystrophy|_osteodystrophy|_impaired_intellectual_development|_and_seizures_syndrome": 1,
    "PIGF-related_condition": 2,
    "Onychodystrophy|_osteodystrophy|_impaired_intellectual_development|_and_seizures_syndrome|not_specified": 1,
    "PIGF-related_condition|not_specified": 1,
    "Rothmund-Thomson_syndrome_type_3": 6,
    "Rothmund-Thomson_syndrome_type_3|Ateleiotic_dwarfism": 2,
    "not_provided|CRIPT-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_3": 1,
    "CRIPT-related_disorder": 2,
    "Factor_5_and_Factor_VIII|_combined_deficiency_of|_2": 93,
    "not_provided|Factor_5_and_Factor_VIII|_combined_deficiency_of|_2": 14,
    "Factor_5_and_Factor_VIII|_combined_deficiency_of|_2|not_provided": 2,
    "Reduced_quantity_of_Von_Willebrand_factor|Reduced_von_Willebrand_factor_activity": 3,
    "not_provided|Factor_5_and_Factor_VIII|_combined_deficiency_of|_2|Thrombocytopenia|Abnormal_bleeding": 1,
    "Thrombocytopenia|Abnormal_bleeding": 5,
    "not_specified|Factor_5_and_Factor_VIII|_combined_deficiency_of|_2": 2,
    "Factor_5_and_Factor_VIII|_combined_deficiency_of|_2|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1|MCFD2-related_disorder": 1,
    "MCFD2-related_disorder": 1,
    "not_provided|TTC7A-related_disorder": 1,
    "Gastrointestinal_defect_and_immunodeficiency_syndrome": 2,
    "Multiple_gastrointestinal_atresias": 688,
    "not_provided|Multiple_gastrointestinal_atresias": 24,
    "Inborn_genetic_diseases|TTC7A-related_disorder": 1,
    "Inborn_genetic_diseases|Multiple_gastrointestinal_atresias": 36,
    "Multiple_gastrointestinal_atresias|Inborn_genetic_diseases|not_provided": 2,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Multiple_gastrointestinal_atresias|Inborn_genetic_diseases": 1,
    "TTC7A-related_disorder|Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Multiple_gastrointestinal_atresias": 6,
    "Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 10,
    "Multiple_gastrointestinal_atresias|Inborn_genetic_diseases": 44,
    "Multiple_gastrointestinal_atresias|not_provided|Gastrointestinal_defect_and_immunodeficiency_syndrome|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Multiple_gastrointestinal_atresias": 2,
    "not_provided|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 3,
    "Multiple_gastrointestinal_atresias|not_specified|not_provided": 3,
    "TTC7A-related_disorder": 4,
    "Multiple_gastrointestinal_atresias|not_provided|TTC7A-related_disorder": 3,
    "not_provided|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Multiple_gastrointestinal_atresias": 1,
    "See_cases|Inborn_genetic_diseases|Multiple_gastrointestinal_atresias": 1,
    "Multiple_gastrointestinal_atresias|TTC7A-related_disorder|Inborn_genetic_diseases": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Inborn_genetic_diseases|Multiple_gastrointestinal_atresias": 1,
    "Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_gastrointestinal_atresias": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 16,
    "Multiple_gastrointestinal_atresias|TTC7A-related_disorder": 9,
    "TTC7A-related_disorder|Multiple_gastrointestinal_atresias": 6,
    "not_provided|Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 2,
    "Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided": 2,
    "TTC7A-related_disorder|Inborn_genetic_diseases|Multiple_gastrointestinal_atresias": 1,
    "not_provided|Multiple_gastrointestinal_atresias|TTC7A-related_disorder": 4,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_specified|Multiple_gastrointestinal_atresias|Common_variable_immunodeficiency": 1,
    "not_provided|not_specified|Multiple_gastrointestinal_atresias": 1,
    "Multiple_gastrointestinal_atresias|not_provided|Inborn_genetic_diseases": 1,
    "Multiple_gastrointestinal_atresias|not_provided": 13,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided": 1,
    "not_specified|not_provided|Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "TTC7A-related_disorder|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "not_specified|not_provided|Multiple_gastrointestinal_atresias": 1,
    "Inborn_genetic_diseases|Multiple_gastrointestinal_atresias|not_provided": 3,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided|Inborn_genetic_diseases|Multiple_gastrointestinal_atresias": 1,
    "Multiple_gastrointestinal_atresias|not_specified": 1,
    "not_specified|Multiple_gastrointestinal_atresias": 2,
    "Multiple_gastrointestinal_atresias|Gastrointestinal_defect_and_immunodeficiency_syndrome": 1,
    "not_provided|TTC7A-related_disorder|Multiple_gastrointestinal_atresias": 1,
    "TTC7A-related_disorder|Multiple_gastrointestinal_atresias|not_provided": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_specified|not_provided|Multiple_gastrointestinal_atresias": 1,
    "not_provided|Multiple_gastrointestinal_atresias|Gastrointestinal_defect_and_immunodeficiency_syndrome": 1,
    "TTC7A-related_disorder|not_provided|Multiple_gastrointestinal_atresias": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Multiple_gastrointestinal_atresias|not_specified|not_provided": 1,
    "Gastrointestinal_defect_and_immunodeficiency_syndrome|Multiple_gastrointestinal_atresias": 2,
    "Inborn_genetic_diseases|Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "not_specified|Multiple_gastrointestinal_atresias|Common_variable_immunodeficiency": 1,
    "not_specified|Multiple_gastrointestinal_atresias|not_provided|TTC7A-related_disorder|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "Multiple_gastrointestinal_atresias|Inborn_genetic_diseases|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "not_specified|Multiple_gastrointestinal_atresias|TTC7A-related_disorder|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided": 1,
    "not_provided|not_specified|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided|not_specified": 1,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_1|not_provided|Multiple_gastrointestinal_atresias": 1,
    "not_provided|not_specified|Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "Severe_combined_immunodeficiency_disease|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|Gastrointestinal_defect_and_immunodeficiency_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Gastrointestinal_defects_and_immunodeficiency_syndrome_1|TTC7A-related_disorder|Multiple_gastrointestinal_atresias": 1,
    "not_specified|Multiple_gastrointestinal_atresias|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "not_provided|Multiple_gastrointestinal_atresias|not_specified|Gastrointestinal_defects_and_immunodeficiency_syndrome_1": 1,
    "not_provided|Long_QT_syndrome_1": 9,
    "not_provided|Long_QT_syndrome_15": 2,
    "not_provided|not_specified|Long_QT_syndrome_1": 2,
    "Long_QT_syndrome_1|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome_15|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_15": 5,
    "Long_QT_syndrome_15|Long_QT_syndrome_1": 5,
    "Long_QT_syndrome_1|Long_QT_syndrome_15": 2,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome_1": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME": 8,
    "Cardiovascular_phenotype|Long_QT_syndrome_1": 15,
    "Inborn_genetic_diseases|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_15|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_15|not_provided|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|not_specified": 3,
    "not_specified|Long_QT_syndrome_15|Long_QT_syndrome_1": 1,
    "not_provided|Long_QT_syndrome_1|not_specified": 1,
    "CALM2-related_disorder": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome_1": 3,
    "not_specified|Long_QT_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome_1|not_provided": 9,
    "Long_QT_syndrome_1|Cardiovascular_phenotype": 12,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Lynch_syndrome": 600,
    "Lynch_syndrome_8": 11,
    "Congenital_diarrhea_5_with_tufting_enteropathy": 24,
    "EPCAM-related_disorder|Familial_cancer_of_breast|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_8": 1,
    "Hereditary_cancer-predisposing_syndrome|EPCAM-related_disorder|not_provided": 3,
    "Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8|not_specified": 1,
    "not_provided|Congenital_diarrhea_5_with_tufting_enteropathy": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 4,
    "Congenital_diarrhea_5_with_tufting_enteropathy|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 85,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_8": 1,
    "not_specified|Lynch_syndrome_8|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_8|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|EPCAM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|EPCAM-related_disorder": 6,
    "not_provided|Lynch_syndrome_8|Lynch_syndrome_1": 1,
    "EPCAM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "EPCAM-related_disorder|not_provided": 1,
    "EPCAM-related_disorder|not_provided|Lynch_syndrome_8": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_8": 1,
    "Lynch_syndrome|not_provided": 41,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_8": 1,
    "not_provided|Lynch_syndrome_8": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_8": 1,
    "EPCAM-related_disorder": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8": 1,
    "Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8|Hereditary_cancer-predisposing_syndrome": 1,
    "EPCAM-related_disorder|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_8": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 5,
    "Congenital_diarrhea_5_with_tufting_enteropathy|not_provided": 2,
    "EPCAM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "EPCAM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|EPCAM-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer": 1,
    "not_provided|Lynch_syndrome": 15,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_8|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8|not_provided": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_8|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_1": 1,
    "not_specified|not_provided|Lynch_syndrome_8": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|EPCAM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Congenital_diarrhea_5_with_tufting_enteropathy": 1,
    "Gastric_cancer|Congenital_diarrhea_5_with_tufting_enteropathy": 2,
    "Lynch_syndrome_8|EPCAM-related_disorder": 1,
    "Lynch_syndrome_8|not_provided|not_specified": 1,
    "EPCAM-related_disorder|not_specified|not_provided|Lynch_syndrome_8|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Congenital_diarrhea_5_with_tufting_enteropathy": 1,
    "not_specified|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8": 1,
    "not_specified|not_provided|Lynch_syndrome_8|Hereditary_cancer-predisposing_syndrome": 1,
    "EPCAM-related_disorder|not_provided|Congenital_diarrhea_5_with_tufting_enteropathy": 1,
    "Lynch_syndrome_8|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_8|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8|not_provided|Familial_cancer_of_breast|EPCAM-related_disorder": 1,
    "Carcinoma_of_colon": 150,
    "not_provided|Congenital_diarrhea_5_with_tufting_enteropathy|Lynch_syndrome_8": 1,
    "EPCAM-related_disorder|Lynch_syndrome_8|Congenital_diarrhea_5_with_tufting_enteropathy|not_specified|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 67,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 99,
    "Hereditary_cancer": 27,
    "Astrocytoma_IDH-mutant|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms": 4386,
    "Lynch_syndrome_1": 473,
    "EPCAM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Lynch_syndrome_8|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_8|not_specified": 1,
    "Lynch_syndrome_8|Lynch_syndrome_1|not_provided|not_specified": 1,
    "Lynch_syndrome_8|EPCAM-related_disorder|not_specified|not_provided": 1,
    "Colonic_neoplasm": 1,
    "not_specified|not_provided|EPCAM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Congenital_diarrhea_5_with_tufting_enteropathy|EPCAM-related_disorder|not_specified": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder": 1,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 126,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Lynch_syndrome_1|not_provided|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 99,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 65,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 78,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 116,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 65,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "not_provided|Lynch_syndrome_1": 3,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 3,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 46,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 46,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 95,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1634,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 116,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1928,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 112,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 27,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 95,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 83,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_provided|not_specified": 1,
    "MSH2-related_disorder|Lynch_syndrome_1|not_specified|not_provided|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Lynch_syndrome": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 116,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 21,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2": 7,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 13,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 76,
    "Lynch_syndrome|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder|Inherited_MMR_deficiency_(Lynch_syndrome)|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 105,
    "Gastric_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 99,
    "Malignant_tumor_of_breast|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|MSH2-related_disorder|Lynch_syndrome_1|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 90,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 11,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 2,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 5,
    "not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 6,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 59,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Ovarian_cancer|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 16,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Lynch_syndrome": 3,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 8,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 63,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 21,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|MSH2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 153,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 21,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 105,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 61,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 6,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 16,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 108,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified": 5,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome": 6,
    "not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 7,
    "not_provided|Malignant_tumor_of_breast|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_1|not_specified|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 10,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1": 1,
    "Lynch_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 19,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 76,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 4,
    "Hereditary_nonpolyposis_colon_cancer": 43,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Malignant_tumor_of_breast|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Malignant_glioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 7,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 3,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 98,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1": 5,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 3,
    "not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 7,
    "Lynch_syndrome_1|Lynch_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_cancer|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Sarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|not_specified": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 11,
    "not_specified|Lynch_syndrome_1": 6,
    "Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Hepatoblastoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Lynch_syndrome_1|Colorectal_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder": 1,
    "Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 7,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 3,
    "Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome_1|Lynch_syndrome": 17,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 2,
    "Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_specified|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome_1|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_1": 1,
    "Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Lynch_syndrome_1": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 11,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 2,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 7,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 4,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 7,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 7,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "not_specified|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 6,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 3,
    "MSH2-related_disorder|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Carcinoma_of_colon|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder|Lynch_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 6,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Breast_carcinoma": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified": 2,
    "Lynch_syndrome|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Carcinoma_of_colon|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 63,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Lynch_syndrome_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch-like_syndrome": 33,
    "MSH2-related_disorder": 6,
    "MSH2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1": 11,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Breast_carcinoma|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_1": 6,
    "Lynch_syndrome_1|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 11,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 38,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 29,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 5,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|MSH2-related_disorder|not_specified": 1,
    "not_provided|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 7,
    "Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 10,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 16,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 3,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 10,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 10,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 2,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Endometrial_carcinoma|Lynch_syndrome": 2,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1": 1,
    "not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 9,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch-like_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "not_provided|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH2-related_disorder|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH2-related_disorder|not_specified|Malignant_tumor_of_breast": 1,
    "not_specified|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|MSH2-related_disorder|Lynch_syndrome|not_provided": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 5,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Malignant_tumor_of_breast": 2,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|not_specified|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|MSH2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_non-polyposis|not_specified|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Carcinoma_of_colon|Breast_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Carcinoma_of_colon": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome|Carcinoma_of_colon|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 2,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Lynch_syndrome_1|not_specified": 1,
    "Lynch_syndrome_1|Ependymoma|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "Familial_colorectal_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_non-polyposis|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome_1": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 92,
    "Lynch_syndrome_1|not_provided": 9,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 48,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1": 1,
    "Carcinoma_of_colon|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|not_provided": 5,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_2|Lynch_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 19,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|MSH2-related_disorder": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 2,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|not_specified|MSH2-related_disorder": 1,
    "not_specified|not_provided|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|MSH2-related_disorder|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 3,
    "Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 17,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|MSH2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 2,
    "Lynch_syndrome_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|MSH2-related_disorder|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 6,
    "Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided": 10,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 27,
    "not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 7,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Intestinal_polyposis_syndrome|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1": 3,
    "Endometrial_carcinoma|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 3,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH2-related_disorder|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 10,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 8,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided": 2,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_1|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Endometrial_carcinoma": 1,
    "Lynch_syndrome_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 7,
    "Colorectal_cancer|_non-polyposis|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|MSH2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 3,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 14,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 2,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 4,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome|Lynch_syndrome_1|Sigmoid_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_non-polyposis|Lynch_syndrome|Lynch_syndrome_1|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome_1|not_provided|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 3,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Bile_duct_cancer": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome_1|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome": 2,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "not_specified|Lynch_syndrome": 4,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome_1|Lynch_syndrome|not_specified": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome": 1,
    "MSH2-related_disorder|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Carcinoma_of_colon|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|not_provided": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_1|MSH2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|MSH2_POLYMORPHISM|Lynch_syndrome_1|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|MSH2-related_disorder|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|not_specified": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Colonic_diverticula|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Lynch_syndrome_1|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Carcinoma_of_colon": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Lynch_syndrome|not_provided|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 5,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome_1|MSH2-related_disorder|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_provided|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1610,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 2,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 3,
    "Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_provided": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|MSH2-related_disorder|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|MSH2-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome": 2,
    "not_specified|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 1,
    "not_specified|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Inherited_ovarian_cancer_(without_breast_cancer)|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_1": 1,
    "not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|MSH2-related_disorder|Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_2|MSH2-related_disorder|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Carcinoma_of_colon|not_provided|MSH2-related_disorder": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Carcinoma_of_colon|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_specified": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH2-related_disorder|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Ovarian_cyst": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Lynch_syndrome_1|Polyp_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_specified|not_provided": 2,
    "Lynch_syndrome|not_specified|not_provided": 6,
    "Lynch_syndrome_1|not_specified": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder": 1,
    "Lynch-like_syndrome|Gastric_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|MSH2-related_disorder|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 8,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Rectal_neoplasm|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 13,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 6,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 3,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_carcinoma": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 3,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "Lynch_syndrome_1|Lynch_syndrome|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Colon_cancer|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch-like_syndrome": 10,
    "not_provided|Carcinoma_of_colon|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)": 4,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome|Breast_and/or_ovarian_cancer|Endometrial_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Familial_cancer_of_breast|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1": 1,
    "not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_provided": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome|Carcinoma_of_colon|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Familial_cancer_of_breast": 1,
    "not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided": 1,
    "MSH2-related_disorder|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Breast_and/or_ovarian_cancer|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|not_provided|MSH2-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_1": 2,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "not_specified|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|not_provided": 1,
    "Lynch_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Lynch-like_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Lynch_syndrome|Uterine_corpus_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "not_provided|not_specified|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|not_specified|Carcinoma_of_colon|not_provided": 1,
    "MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Lynch_syndrome|Uterine_corpus_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|not_provided": 2,
    "not_specified|Lynch_syndrome|MSH2-related_disorder|not_provided|Hereditary_nonpolyposis_colon_cancer|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "not_provided|Ovarian_neoplasm|Lynch-like_syndrome|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|MSH2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "Lynch_syndrome_1|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|not_provided|Lynch_syndrome": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 1,
    "Breast_and/or_ovarian_cancer": 58,
    "not_provided|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome|MSH2-related_disorder|not_provided": 1,
    "Colorectal_cancer|_non-polyposis|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Malignant_tumor_of_breast|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome": 9,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided": 1,
    "Lynch_syndrome_1|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|MSH2-related_disorder|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colon_cancer|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Breast_carcinoma": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|not_provided|not_specified|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|not_provided|not_specified|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Ovarian_cancer|not_specified|Mismatch_repair_cancer_syndrome_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Carcinoma_of_colon|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 2,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 4,
    "Lynch_syndrome|not_provided|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|MSH2-related_disorder|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 204,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "not_specified|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Malignant_tumor_of_ascending_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_1|not_provided|Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|not_specified": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast": 5,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_provided|Breast_and/or_ovarian_cancer|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "not_provided|Lynch_syndrome|Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|MSH2-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome_1": 1,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|not_provided|not_specified|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Malignant_tumor_of_breast|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|not_provided": 1,
    "Lynch_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 15,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Carcinoma_of_colon|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Lynch_syndrome_1|Ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Cancer_or_benign_tumor|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch-like_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Lynch_syndrome_1|Lynch-like_syndrome|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 3,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 11,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|not_provided": 2,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_1|not_provided|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH2-related_disorder|Colorectal_cancer|not_specified|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Gastric_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|not_specified|MSH2-related_disorder|Lynch_syndrome": 1,
    "Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Colon_cancer": 4,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|MSH2-related_disorder|Malignant_tumor_of_breast|not_specified|Hereditary_nonpolyposis_colon_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_non-polyposis|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Malignant_tumor_of_breast|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|not_specified": 1,
    "Uterine_corpus_cancer": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|not_specified|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_cancer|not_specified|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "Lynch_syndrome_1|Ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_specified|Lynch_syndrome": 1,
    "not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified|not_provided": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 7,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Familial_colorectal_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH2-related_disorder|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_specified": 1,
    "Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|MSH2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|See_cases": 1,
    "Malignant_tumor_of_breast|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 3,
    "Lynch_syndrome|Lynch_syndrome_1|not_specified|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_non-polyposis|not_provided": 1,
    "not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH2-related_disorder|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_1|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "MSH2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|not_provided|not_specified": 1,
    "not_provided|Lynch_syndrome_5": 9,
    "Lynch_syndrome_5": 441,
    "not_specified|Lynch_syndrome_5": 6,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 139,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 88,
    "MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|MSH6-related_disorder|Malignant_tumor_of_breast|Lynch_syndrome_5|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_provided|MSH6-related_disorder|not_specified": 1,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 117,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 110,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 139,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 73,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Carcinoma_of_colon|Breast_and/or_ovarian_cancer|MSH6-related_disorder|Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 110,
    "Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 12,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 89,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5": 8,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 13,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma": 8,
    "Lynch_syndrome|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 13,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_specified|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Lynch_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "MSH6-related_disorder": 8,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Colorectal_/_endometrial_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 109,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 130,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5": 23,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Mismatch_repair_cancer_syndrome_3": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Endometrial_carcinoma|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 8,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified": 7,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 8,
    "Lynch_syndrome|MSH6-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 56,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 10,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_5|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 9,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_5|MSH6-related_disorder|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "Carcinoma_of_colon|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|not_specified": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ovarian_cancer|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_5|Lynch_syndrome_1|Breast_carcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 5,
    "Carcinoma_of_colon|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 19,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 10,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 2,
    "Lynch_syndrome_5|Lynch_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 11,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 18,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "not_specified|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 10,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH6-related_disorder": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|not_provided|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 10,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 10,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 18,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 28,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_5|not_provided": 17,
    "Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 5,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Lynch_syndrome|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_provided|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 3,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_5": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 8,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 13,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Lynch_syndrome_5|Endometrial_carcinoma": 6,
    "Familial_cancer_of_breast|not_provided": 109,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Lynch_syndrome_5|Breast_and/or_ovarian_cancer|not_specified|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 11,
    "Lynch_syndrome_5|not_provided|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hepatoblastoma|Hereditary_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Ovarian_neoplasm|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Endometrial_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma|Lynch_syndrome|Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 4,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 5,
    "not_provided|Endometrial_carcinoma": 16,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_non-polyposis|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5": 5,
    "not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 3,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "MSH6-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome_5|not_specified": 1,
    "MSH6-related_disorder|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_5": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 6,
    "Lynch_syndrome_5|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 5,
    "MSH6-related_disorder|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 24,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 4,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5": 4,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "not_specified|Malignant_tumor_of_breast|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 8,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 6,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma": 1,
    "Ovarian_neoplasm": 89,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 3,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 5,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma": 4,
    "not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 5,
    "Familial_cancer_of_breast|Lynch_syndrome|not_specified|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_5": 2,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 3,
    "not_specified|Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Lynch_syndrome_5|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "MSH6-related_disorder|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Malignant_tumor_of_breast|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Abnormality_of_the_ovary|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Endometrial_carcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 15,
    "Carcinoma_of_colon|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 3,
    "Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 3,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5": 2,
    "Uterine_corpus_cancer|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Malignant_tumor_of_breast": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 2,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 4,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "not_provided|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|not_specified|Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5": 7,
    "not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 5,
    "Lynch_syndrome|Lynch_syndrome_5": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided": 3,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 6,
    "not_specified|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5": 4,
    "Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|not_specified": 1,
    "Endometrial_carcinoma|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_provided": 1,
    "MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Breast_and/or_ovarian_cancer|not_provided|Lynch_syndrome_5|not_specified": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome|Breast_and/or_ovarian_cancer|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Mismatch_repair_cancer_syndrome_3|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Lynch_syndrome_5|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_5|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_carcinoma|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 38,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 3,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 8,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Endometrial_carcinoma|Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Mismatch_repair_cancer_syndrome_3|Breast_and/or_ovarian_cancer|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 12,
    "not_provided|not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|not_provided": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|MSH6-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 3,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|not_specified|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Breast_and/or_ovarian_cancer|not_specified|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 9,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 2,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_nonpolyposis_colon_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "not_provided|Lynch_syndrome|not_specified|MSH6-related_disorder|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 4,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Carcinoma_of_colon|not_specified|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_5": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome_5": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|not_specified|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|Lynch_syndrome": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 4,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 5,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "MSH6-related_disorder|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 2,
    "not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 5,
    "Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|MSH6-related_disorder": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 6,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|not_provided": 2,
    "Lynch_syndrome_5|not_provided|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5": 2,
    "Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|not_provided": 20,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "not_provided|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 1,
    "not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_1": 8,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Endometrial_carcinoma|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified": 4,
    "Lynch_syndrome|not_provided|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Endometrial_carcinoma|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Lynch_syndrome|not_specified|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Lynch_syndrome_1|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|Prostate_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|not_specified|MSH6-related_disorder|Carcinoma_of_colon|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5": 2,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Lynch_syndrome": 8,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_5|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|not_provided|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Breast_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 4,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Endometrial_carcinoma|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Carcinoma_of_colon|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Gastric_cancer|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 34,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome_5|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 4,
    "Breast_and/or_ovarian_cancer|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|not_specified": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_5": 1,
    "not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 2,
    "Hereditary_nonpolyposis_colon_cancer|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_5|MSH6-related_disorder": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|not_specified|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|MSH6-related_disorder|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5": 1,
    "Colon_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma|Lynch_syndrome_5|Lynch_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_5|Lynch_syndrome|MSH6-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|MSH6-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 4,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|not_provided": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|MSH6-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|not_provided|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome_5|Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|Endometrial_carcinoma|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_specified|Endometrial_carcinoma|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Lynch_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_specified|Malignant_tumor_of_breast|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|MSH6-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 14,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome_5|Lynch_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|not_provided": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|MSH6-related_disorder": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5": 2,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 2,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "not_specified|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Lung_sarcomatoid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Familial_cancer_of_breast": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_1|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MSH6-related_disorder|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_5": 2,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Inherited_MMR_deficiency_(Lynch_syndrome)|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch-like_syndrome": 1,
    "MSH6-related_disorder|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 2,
    "Lynch_syndrome_1|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|MSH6-related_disorder|Carcinoma_of_colon": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 4,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 15,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_5|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "not_specified|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|not_specified|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 1,
    "not_provided|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_5|Lynch_syndrome|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_5|Lynch_syndrome|not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|not_provided": 2,
    "Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5": 6,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Lynch_syndrome": 3,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2818,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Rhabdomyosarcoma|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Carcinoma_of_colon": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome_5|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_provided|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 2,
    "Carcinoma_of_colon|MSH6-related_disorder|Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 2,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|not_specified|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome|Lynch-like_syndrome": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_5|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2206,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 2,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|MSH6-related_disorder|Endometrial_carcinoma|not_provided|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Breast_and/or_ovarian_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma": 4,
    "Lynch_syndrome_5|Carcinoma_of_colon|Mismatch_repair_cancer_syndrome_3|Ovarian_carcinoma|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast": 2,
    "B_Lymphoblastic_Leukemia/Lymphoma_with_t(9%3B22)(q34.1%3Bq11.2)%3B_BCR-ABL1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Endometrial_carcinoma": 2,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "not_specified|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|MSH6-related_disorder|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 2,
    "Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_/_endometrial_cancer|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_colon|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 2,
    "Mismatch_repair_cancer_syndrome_3|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|not_provided|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|MSH6-related_disorder|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Carcinoma_of_colon|Hereditary_nonpolyposis_colon_cancer|Endometrial_carcinoma|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome": 1,
    "Endometrial_carcinoma|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Lynch_syndrome_5": 2,
    "Cerebellar_medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon|Breast_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|MSH6-related_disorder|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified|Lynch_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Uterine_corpus_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Gastric_cancer|Lynch_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Endometrial_carcinoma|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 4,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Endometrial_carcinoma|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma": 2,
    "Lynch-like_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Malignant_tumor_of_breast|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "MSH6-related_disorder|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Endometrial_carcinoma|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome|not_provided|Malignant_tumor_of_breast|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Lynch_syndrome_1": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|not_specified|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma|Lynch_syndrome|not_provided|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 1,
    "not_specified|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_5|not_specified|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_5|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|Endometrial_carcinoma|not_provided|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 2,
    "not_specified|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 2,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_5|not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Lynch_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Carcinoma_of_colon|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Breast_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma": 2,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Breast_and/or_ovarian_cancer|Lynch_syndrome": 1,
    "Lynch_syndrome|not_provided|not_specified": 5,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|not_provided": 1,
    "not_provided|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MSH6-related_disorder|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Lynch_syndrome|Endometrial_carcinoma|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "not_provided|Lynch_syndrome_5|not_specified|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_nonpolyposis_colon_cancer|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma|Lynch_syndrome_5|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Lynch_syndrome|Carcinoma_of_colon": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|not_specified|MSH6-related_disorder|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|MSH6-related_disorder|Inherited_prostate_cancer|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colon_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome_1|Breast_carcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|Lynch_syndrome|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Gastric_cancer|Lynch_syndrome": 1,
    "Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Carcinoma_of_colon|Lynch_syndrome_1|Lynch_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Breast_and/or_ovarian_cancer|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome_5|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|MSH6-related_disorder|Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch-like_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Lynch_syndrome|Breast_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|MSH6-related_disorder|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Carcinoma_of_colon|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified": 1,
    "not_specified|Lynch_syndrome|Malignant_tumor_of_breast|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5|not_provided": 1,
    "Lynch_syndrome|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_5|Carcinoma_of_colon|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|not_provided|Lynch_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_specified|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma": 2,
    "Lynch_syndrome_5|Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|Carcinoma_of_colon": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome_5|not_provided|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|not_provided": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome|Endometrial_carcinoma|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome_5|not_provided|Inherited_MMR_deficiency_(Lynch_syndrome)|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5": 1,
    "Lynch-like_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Papillary_carcinoma_of_the_corpus_uteri|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Lynch_syndrome_1": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_1|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified": 1,
    "MSH6-related_disorder|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Mismatch_repair_cancer_syndrome_3|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|not_provided": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Lynch_syndrome_5|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|MSH6-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|not_specified|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Familial_cancer_of_breast": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "not_provided|Mismatch_repair_cancer_syndrome_3": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Familial_cancer_of_breast": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|not_provided|not_specified|Carcinoma_of_colon|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Lynch_syndrome": 1,
    "MSH6-related_disorder|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "not_provided|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|not_specified": 3,
    "Lynch_syndrome_5|not_provided|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_5|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 5,
    "Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_5|not_specified|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Malignant_tumor_of_breast|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|not_provided": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Malignant_tumor_of_breast|Lynch_syndrome|not_specified|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided": 1,
    "Lynch_syndrome_5|not_provided|not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Gastric_cancer|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|MSH6-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Endometrial_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "not_provided|Lynch_syndrome|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|bilateral_breast_cancer": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Lynch_syndrome_5|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_specified|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Malignant_tumor_of_breast": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided": 1,
    "not_provided|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_carcinoma_of_the_corpus_uteri|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_5|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "not_specified|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Gaucher_disease_type_I": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|not_provided": 1,
    "not_specified|Lynch_syndrome_5|not_provided|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_provided": 1,
    "Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|Carcinoma_of_colon|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|not_specified": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Carcinoma_of_colon": 1,
    "Lynch_syndrome|Endometrial_carcinoma": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_5|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Carcinoma_of_colon": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|not_provided": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_early_onset|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Malignant_tumor_of_breast": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colorectal_carcinoma|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch-like_syndrome|not_provided": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma|Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5|Endometrial_carcinoma|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_3|Gastric_cancer|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Lynch_syndrome": 1,
    "MSH6-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_provided|Lynch_syndrome": 1,
    "not_specified|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_provided|not_specified|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Breast_and/or_ovarian_cancer|MSH6-related_disorder|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_5|MSH6-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified|Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_5": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided|not_specified|Lynch_syndrome_5": 1,
    "not_provided|MSH6-related_disorder|not_specified": 1,
    "not_provided|not_specified|Lynch_syndrome_5": 1,
    "not_provided|not_specified|Lynch_syndrome_5|Breast_and/or_ovarian_cancer": 1,
    "not_provided|not_specified|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|not_provided|Lynch_syndrome_5": 1,
    "not_provided|Breast_and/or_ovarian_cancer|not_specified|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_specified|not_provided|Breast_and/or_ovarian_cancer|Lynch_syndrome_5": 1,
    "not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_provided|not_specified": 1,
    "not_specified|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Lynch_syndrome_5|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Lynch_syndrome_5": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Carcinoma_of_colon|See_cases": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_3|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|MSH6-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Carcinoma_of_colon|not_provided|Lynch_syndrome_5": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_specified|not_provided|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|Lynch_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_5|Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|not_provided|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_5|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome_5|not_provided|Hereditary_nonpolyposis_colon_cancer|not_specified|Lynch_syndrome_1|Lynch_syndrome|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Sigmoid_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|MSH6-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Lynch_syndrome_5|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_nonpolyposis_colorectal_neoplasms|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_5|Lynch_syndrome": 1,
    "not_provided|MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_5|not_specified": 1,
    "not_provided|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_3": 1,
    "Lynch_syndrome|MSH6-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH6-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_5|not_specified": 1,
    "not_provided|Mismatch_repair_cancer_syndrome_3|Endometrial_carcinoma|Lynch_syndrome_5": 1,
    "Endometrial_carcinoma|Mismatch_repair_cancer_syndrome_3|Lynch_syndrome_5|not_provided|Familial_cancer_of_breast|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Endometrial_carcinoma|Lynch_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 113,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Neurodevelopmental_disorder": 2,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_provided|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Neurodevelopmental_disorder": 2,
    "not_specified|not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "not_provided|FBXO11-related_disorder": 9,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 9,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_provided": 13,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Neurodevelopmental_disorder|not_provided": 1,
    "FBXO11-related_disorder": 6,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|FBXO11-related_disorder|not_provided": 1,
    "FBXO11-related_disorder|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_provided": 1,
    "FBXO11-related_disorder|not_provided": 3,
    "not_provided|Neurodevelopmental_disorder": 24,
    "Marfanoid_habitus_and_intellectual_disability|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Neurodevelopmental_disorder": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Delayed_speech_and_language_development": 1,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 1,
    "not_provided|FBXO11-related_disorder|not_specified": 1,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_specified": 1,
    "not_provided|Developmental_disorder": 4,
    "FBXO11-related_disorder|Inborn_genetic_diseases|Intellectual_disability|not_provided": 1,
    "not_provided|FBXO11-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_facial_dysmorphism|_and_brain_abnormalities": 19,
    "PPP1R21-related_disorder": 15,
    "not_provided|PPP1R21-related_disorder": 1,
    "PPP1R21-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_facial_dysmorphism|_and_brain_abnormalities|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_facial_dysmorphism|_and_brain_abnormalities": 1,
    "Inborn_genetic_diseases|not_provided|PPP1R21-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|Neurodevelopmental_disorder_with_hypotonia|_facial_dysmorphism|_and_brain_abnormalities": 1,
    "Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis": 15,
    "Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity": 10,
    "Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|Hypergonadotropic_hypogonadism": 7,
    "Hypergonadotropic_hypogonadism|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity": 5,
    "not_provided|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|Hypergonadotropic_hypogonadism": 3,
    "Hypergonadotropic_hypogonadism|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|not_provided": 3,
    "Hypergonadotropic_hypogonadism|not_provided|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity": 3,
    "Gonadotropin-independent_familial_sexual_precocity|not_specified|Leydig_cell_agenesis": 1,
    "Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|not_provided": 3,
    "Leydig_cell_hypoplasia|_type_II": 3,
    "Leydig_cell_agenesis": 14,
    "Leydig_cell_agenesis|Inborn_genetic_diseases": 1,
    "not_provided|Leydig_cell_agenesis|Leydig_hypoplasia|_type_I": 1,
    "Luteinizing_hormone_resistance|_female|Leydig_cell_agenesis": 2,
    "Leydig_cell_agenesis|Luteinizing_hormone_resistance|_female": 1,
    "Precocious_puberty_in_males|Gonadotropin-independent_familial_sexual_precocity|not_provided|Leydig_cell_agenesis": 1,
    "Gonadotropin-independent_familial_sexual_precocity": 7,
    "Leydig_cell_adenoma|_somatic|_with_male-limited_precocious_puberty": 1,
    "Gonadotropin-independent_familial_sexual_precocity|not_provided": 4,
    "Hypergonadotropic_hypogonadism|not_provided|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis": 1,
    "Disorder_of_sexual_differentiation|not_provided|Leydig_cell_agenesis|Luteinizing_hormone_resistance|_female|See_cases": 1,
    "Leydig_cell_agenesis|not_provided|Gonadotropin-independent_familial_sexual_precocity": 1,
    "Gonadotropin-independent_familial_sexual_precocity|LHCGR-related_disorder|not_provided": 1,
    "Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis|not_provided": 1,
    "Precocious_puberty_in_males|Gonadotropin-independent_familial_sexual_precocity": 1,
    "not_provided|not_specified|Hypergonadotropic_hypogonadism|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis": 1,
    "Leydig_cell_agenesis|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hypergonadotropic_hypogonadism|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|not_specified": 1,
    "LHCGR-related_disorder": 5,
    "Hypergonadotropic_hypogonadism|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis|not_specified|not_provided": 1,
    "not_provided|Hypergonadotropic_hypogonadism|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis|not_specified": 1,
    "46|XY_disorder_of_sex_development": 15,
    "not_provided|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis": 2,
    "not_provided|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis|not_specified": 1,
    "Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|not_provided|Hypergonadotropic_hypogonadism|LHCGR-related_disorder|not_specified": 1,
    "LHCGR-related_disorder|not_provided|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|Hypergonadotropic_hypogonadism": 1,
    "Pseudohermaphroditism": 4,
    "not_provided|LHCGR-related_disorder": 1,
    "Leydig_cell_agenesis|not_provided": 1,
    "not_specified|not_provided|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis": 1,
    "not_provided|Leydig_cell_agenesis": 2,
    "Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis|Hypergonadotropic_hypogonadism|not_provided": 1,
    "Leydig_cell_agenesis|not_provided|Gonadotropin-independent_familial_sexual_precocity|Hypergonadotropic_hypogonadism": 1,
    "LHCGR-related_disorder|not_provided": 1,
    "Disorder_of_sexual_differentiation|not_provided|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity": 1,
    "LHCGR-related_disorder|Leydig_cell_agenesis|not_provided": 1,
    "not_provided|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|Hypergonadotropic_hypogonadism|LHCGR-related_disorder|not_specified": 1,
    "LHCGR-related_disorder|not_provided|Gonadotropin-independent_familial_sexual_precocity|not_specified|Leydig_cell_agenesis": 1,
    "Hypergonadotropic_hypogonadism|not_provided|not_specified|Luteinizing_hormone/choriogonadotropin_receptor|_lq_variant|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity": 1,
    "LHCGR-related_disorder|Leydig_cell_agenesis|Gonadotropin-independent_familial_sexual_precocity|Hypergonadotropic_hypogonadism": 1,
    "STON1-GTF2A1L-related_disorder": 1,
    "not_provided|Hypergonadotropic_hypogonadism|Gonadotropin-independent_familial_sexual_precocity|Leydig_cell_agenesis": 1,
    "Ovarian_hyperstimulation_syndrome|Ovarian_dysgenesis_1": 18,
    "Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome": 12,
    "Ovarian_hyperstimulation_syndrome|Ovarian_dysgenesis_1|not_provided": 4,
    "Ovarian_hyperstimulation_syndrome|Ovarian_dysgenesis": 3,
    "not_specified|Ovarian_hyperstimulation_syndrome|Ovarian_dysgenesis_1|not_provided": 1,
    "Ovarian_dysgenesis_1": 16,
    "FSHR-related_disorder|not_provided": 2,
    "Ovarian_hyperstimulation_syndrome": 6,
    "Ovarian_hyperstimulation_syndrome|Ovarian_dysgenesis_1|Inborn_genetic_diseases": 5,
    "not_provided|Ovarian_hyperstimulation_syndrome|Ovarian_dysgenesis_1": 1,
    "Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome": 2,
    "Ovarian_hyperstimulation_syndrome|Dizygotic_twins|Ovarian_dysgenesis_1": 2,
    "not_provided|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|Gonadal_dysgenesis": 1,
    "Inborn_genetic_diseases|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome": 1,
    "Hereditary_xanthinuria_type_1|Dizygotic_twins": 1,
    "FSHR-related_disorder": 1,
    "not_provided|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|not_specified": 2,
    "Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|not_provided": 1,
    "not_provided|FSHR-related_disorder|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome": 1,
    "FSHR-related_disorder|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|not_provided": 1,
    "Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome|not_specified|not_provided|FSHR-related_disorder": 1,
    "Amenorrhea": 18,
    "Inborn_genetic_diseases|FSHR-related_disorder": 1,
    "not_specified|not_provided|Ovarian_dysgenesis_1|Ovarian_hyperstimulation_syndrome": 1,
    "Ovarian_hyperstimulation_syndrome|not_provided|Ovarian_dysgenesis": 1,
    "Pitt-Hopkins-like_syndrome": 24,
    "Pitt-Hopkins-like_syndrome_2": 1308,
    "Pitt-Hopkins-like_syndrome_2|not_provided": 103,
    "not_provided|Pitt-Hopkins-like_syndrome": 6,
    "Pitt-Hopkins-like_syndrome_2|not_specified": 31,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases": 45,
    "not_provided|Pitt-Hopkins-like_syndrome_2": 84,
    "Pitt-Hopkins-like_syndrome_2|not_provided|Inborn_genetic_diseases": 7,
    "History_of_neurodevelopmental_disorder": 15,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Pitt-Hopkins-like_syndrome_2": 2,
    "NRXN1-related_disorder": 13,
    "Schizophrenia_17": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|not_specified|History_of_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|not_provided": 17,
    "not_specified|not_provided|History_of_neurodevelopmental_disorder|Pitt-Hopkins-like_syndrome_2": 1,
    "Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2": 4,
    "Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2|not_specified|not_provided": 1,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2": 44,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_provided": 8,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_specified": 3,
    "not_specified|Pitt-Hopkins-like_syndrome_2": 22,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|Inborn_genetic_diseases|NRXN1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Pitt-Hopkins-like_syndrome_2|not_provided": 1,
    "Gestational_diabetes_mellitus_uncontrolled": 23,
    "Inborn_genetic_diseases|not_provided|Pitt-Hopkins-like_syndrome_2": 12,
    "See_cases|Pitt-Hopkins-like_syndrome_2": 1,
    "Chromosome_2p16.3_deletion_syndrome": 1,
    "not_specified|History_of_neurodevelopmental_disorder|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder|not_provided": 1,
    "Pitt-Hopkins-like_syndrome_2|not_provided|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases": 3,
    "not_provided|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome": 2,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 5,
    "not_specified|NRXN1-related_disorder|not_provided|Pitt-Hopkins-like_syndrome_2": 1,
    "Pitt-Hopkins-like_syndrome_2|not_provided|not_specified": 1,
    "not_provided|not_specified|Pitt-Hopkins-like_syndrome_2": 2,
    "Inborn_genetic_diseases|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided": 1,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided|Obesity": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|Autism_spectrum_disorder": 1,
    "History_of_neurodevelopmental_disorder|Pitt-Hopkins-like_syndrome_2|not_specified": 1,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome": 6,
    "not_provided|NRXN1-related_disorder": 1,
    "NRXN1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "NRXN1-related_disorder|not_provided": 3,
    "not_provided|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|Inborn_genetic_diseases": 2,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|NRXN1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|NRXN1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|NRXN1-related_disorder": 1,
    "Inborn_genetic_diseases|Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2|not_provided": 1,
    "Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2|not_provided": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2": 3,
    "not_specified|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_provided": 2,
    "Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 5,
    "not_specified|not_provided|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Pitt-Hopkins-like_syndrome_2": 10,
    "Pitt-Hopkins-like_syndrome_2|Intellectual_disability": 1,
    "not_provided|not_specified|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided|not_specified|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|not_provided|Chromosome_2p16.3_deletion_syndrome": 1,
    "Inborn_genetic_diseases|Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2|not_specified|not_provided": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Pitt-Hopkins-like_syndrome_2": 3,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2": 1,
    "NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|Pitt-Hopkins-like_syndrome_2": 1,
    "Pitt-Hopkins-like_syndrome_2|not_specified|Inborn_genetic_diseases": 3,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|NRXN1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_specified|not_provided": 1,
    "Pitt-Hopkins-like_syndrome_2|not_specified|not_provided": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2": 1,
    "Inborn_genetic_diseases|not_specified|Pitt-Hopkins-like_syndrome_2": 1,
    "NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|not_provided|Chromosome_2p16.3_deletion_syndrome": 1,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder|not_specified": 2,
    "not_specified|not_provided|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 2,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|NRXN-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder|Intellectual_disability": 1,
    "not_specified|NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|not_provided": 2,
    "not_specified|Pitt-Hopkins-like_syndrome_2|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2": 1,
    "NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2|not_specified": 1,
    "NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Pitt-Hopkins-like_syndrome_2|not_provided|NRXN1-related_disorder": 1,
    "not_specified|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|Intellectual_disability": 1,
    "not_provided|Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder": 1,
    "not_specified|Chromosome_2p16.3_deletion_syndrome|Pitt-Hopkins-like_syndrome_2": 1,
    "NRXN1-related_disorder|not_provided|Pitt-Hopkins-like_syndrome_2": 1,
    "Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "NRXN1-related_disorder|Pitt-Hopkins-like_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided|Intellectual_disability": 1,
    "Pitt-Hopkins-like_syndrome_2|NRXN1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|not_provided|Intellectual_disability|NRXN1-related_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases|not_provided|Chromosome_2p16.3_deletion_syndrome": 1,
    "not_specified|Pitt-Hopkins-like_syndrome_2|Inborn_genetic_diseases": 1,
    "See_cases|not_provided|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome_2|Chromosome_2p16.3_deletion_syndrome|Complex_neurodevelopmental_disorder": 1,
    "Pitt-Hopkins-like_syndrome_2|Ovarian_dysgenesis_3": 1,
    "Pitt-Hopkins-like_syndrome|not_provided": 2,
    "Preeclampsia|Normal_pregnancy|Large_for_gestational_age|Gestational_diabetes_mellitus_uncontrolled": 2,
    "Mandibular_prognathia": 4,
    "GPR75-related_disorder": 9,
    "Chronic_osteomyelitis": 5,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities": 92,
    "SPTBN1-related_disorder": 26,
    "Autistic_behavior|Intellectual_disability": 2,
    "SPTBN1-related_neurodevelopmental_disease": 2,
    "SPTBN1-related_disorder|not_provided": 1,
    "not_provided|SPTBN1-related_disorder": 6,
    "Pervasive_developmental_disorder|Intellectual_disability|_autosomal_recessive_53": 1,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures|not_provided": 1,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "Atypical_behavior|Mild_global_developmental_delay": 1,
    "not_provided|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities": 2,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "SPTBN1-related_disorder|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities": 1,
    "Inborn_genetic_diseases|SPTBN1-related_disorder": 2,
    "Moderate_global_developmental_delay": 3,
    "Inborn_genetic_diseases|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities": 1,
    "Inborn_genetic_diseases|SPTBN1-related_disorder|not_provided": 1,
    "Marked_Hypotonia|Waddling_gait": 1,
    "not_provided|CCDC88A-related_disorder": 5,
    "PEHO_syndrome|not_specified|not_provided": 1,
    "not_provided|PEHO-like_syndrome": 6,
    "CCDC88A-related_disorder|not_provided": 6,
    "PEHO-like_syndrome|not_provided": 3,
    "PEHO-like_syndrome": 7,
    "Autism_spectrum_disorder|Developmental_delay|PEHO-like_syndrome|not_provided": 1,
    "not_provided|CCDC88A-related_disorder|PEHO-like_syndrome": 1,
    "Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_70": 4,
    "Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|Spinocerebellar_ataxia_type_25|PNPT1-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia_type_25": 6,
    "PNPT1-related_disorder|not_provided": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_70|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_13": 18,
    "Autosomal_recessive_nonsyndromic_hearing_loss_70": 6,
    "not_provided|Spinocerebellar_ataxia_type_25|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70": 3,
    "not_provided|Hereditary_ataxia|Inborn_genetic_diseases": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_13": 4,
    "not_provided|PNPT1-related_disorder": 11,
    "Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|not_provided": 4,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70": 2,
    "PNPT1-related_disorder|not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70": 1,
    "PNPT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_13|not_provided": 3,
    "Spinocerebellar_ataxia_type_25|PNPT1-related_disorder|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_25|Neurodevelopmental_disorder|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|not_provided": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_13|not_provided": 1,
    "PNPT1-related_disorder": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_70|not_specified|Combined_oxidative_phosphorylation_defect_type_13|not_provided": 1,
    "PNPT1-related_disorder|not_specified|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_13|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70": 1,
    "not_provided|PNPT1-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_70|Spinocerebellar_ataxia_type_25": 1,
    "PNPT1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_70": 1,
    "PNPT1-related_disorder|not_provided|not_specified": 1,
    "Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|PNPT1-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70": 1,
    "not_provided|PNPT1-related_disorder|not_specified": 1,
    "Spinocerebellar_ataxia_type_25|not_specified|Combined_oxidative_phosphorylation_defect_type_13|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_13": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|not_provided": 1,
    "not_provided|Hereditary_ataxia": 2,
    "PNPT1-related_disorder|See_cases|not_provided": 1,
    "PNPT1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_25|Combined_oxidative_phosphorylation_defect_type_13|Autosomal_recessive_nonsyndromic_hearing_loss_70|Inborn_genetic_diseases|not_provided": 1,
    "Doyne_honeycomb_retinal_dystrophy": 24,
    "not_provided|Doyne_honeycomb_retinal_dystrophy": 19,
    "Doyne_honeycomb_retinal_dystrophy|not_provided": 15,
    "Retinal_dystrophy|Doyne_honeycomb_retinal_dystrophy|not_specified|not_provided": 1,
    "Glaucoma_1|_open_angle|_H|not_provided|Glaucoma_of_childhood": 1,
    "Cutis_laxa|Cutis_laxa|_autosomal_recessive|_type_1d": 1,
    "Macular_dystrophy|Optic_disc_drusen|Retinal_pigment_epithelial_atrophy|Night_blindness|Blindness": 1,
    "EFEMP1-related_connective_tissue_condition": 1,
    "Retinal_dystrophy|not_provided|Doyne_honeycomb_retinal_dystrophy": 1,
    "Doyne_honeycomb_retinal_dystrophy|not_provided|not_specified": 1,
    "EFEMP1-related_disorder|not_provided": 3,
    "EFEMP1-related_disorder": 1,
    "Optic_atrophy|not_provided|Inborn_genetic_diseases": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1d|Diverticulum_of_bladder|Generalized_hypotonia|Joint_hypermobility|Tall_stature|Arachnodactyly|Inguinal_hernia|Scoliosis|Pulmonary_bulla|Posterolateral_diaphragmatic_hernia|High_myopia|Dural_ectasia|Ectropion_of_lower_eyelids|Accelerated_skeletal_maturation|Dolichocephaly": 2,
    "not_provided|EFEMP1-related_disorder": 2,
    "not_specified|not_provided|Doyne_honeycomb_retinal_dystrophy": 1,
    "Glaucoma_1|_open_angle|_H|Retinal_dystrophy|not_provided|Doyne_honeycomb_retinal_dystrophy": 1,
    "Doyne_honeycomb_retinal_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1d|Doyne_honeycomb_retinal_dystrophy|Glaucoma_1|_open_angle|_H|not_provided": 1,
    "not_specified|Doyne_honeycomb_retinal_dystrophy|not_provided": 1,
    "Glaucoma_1|_open_angle|_H|Glaucoma_of_childhood": 1,
    "not_provided|Recessive_Marfanoid_Syndrome_with_Severe_Herniation|Cutis_laxa|_autosomal_recessive|_type_1d": 1,
    "EFEMP1-related_disorder|not_provided|Doyne_honeycomb_retinal_dystrophy": 1,
    "Fanconi_anemia_complementation_group_L": 69,
    "Fanconi_anemia": 9094,
    "Fanconi_anemia_complementation_group_L|not_provided": 6,
    "Fanconi_anemia_complementation_group_L|not_specified": 1,
    "not_provided|Fanconi_anemia_complementation_group_L": 3,
    "Inborn_genetic_diseases|Fanconi_anemia": 708,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_L|not_specified": 1,
    "FANCL-related_disorder|Hereditary_cancer|not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_L": 37,
    "Fanconi_anemia_complementation_group_L|Fanconi_anemia": 46,
    "not_provided|Fanconi_anemia_complementation_group_L|Fanconi_anemia": 2,
    "Fanconi_anemia|not_provided": 243,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_L": 3,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_L|Fanconi_anemia": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified|Fanconi_anemia_complementation_group_L": 1,
    "not_provided|Fanconi_anemia|FANCL-related_disorder|Fanconi_anemia_complementation_group_L|not_specified|Premature_ovarian_insufficiency": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_L|not_provided|not_specified": 2,
    "Fanconi_anemia_complementation_group_L|Inborn_genetic_diseases": 2,
    "Fanconi_anemia_complementation_group_L|Fanconi_anemia|FANCL-related_disorder|not_specified": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 2,
    "Fanconi_anemia_complementation_group_L|Fanconi_anemia|not_provided": 4,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_L": 2,
    "Fanconi_anemia|FANCL-related_disorder|Fanconi_anemia_complementation_group_L": 1,
    "Fanconi_anemia|Inborn_genetic_diseases": 634,
    "Fanconi_anemia|FANCL-related_disorder": 2,
    "Fanconi_anemia|not_specified": 79,
    "not_provided|Fanconi_anemia": 236,
    "FANCL-related_disorder": 2,
    "Fanconi_anemia_complementation_group_A": 520,
    "Fanconi_anemia|not_provided|not_specified": 2,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia": 210,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_L|not_specified|FANCL-related_disorder": 1,
    "Fanconi_anemia_complementation_group_L|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_L": 2,
    "Fanconi_anemia_complementation_group_L|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "FANCL-related_disorder|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_L|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_L|Inborn_genetic_diseases": 1,
    "not_specified|Fanconi_anemia_complementation_group_L|not_provided": 2,
    "not_specified|Fanconi_anemia": 60,
    "not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_L|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_L|not_provided|Fanconi_anemia": 1,
    "VATER_association|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 1,
    "Fanconi_anemia_complementation_group_L|See_cases|Fanconi_anemia|not_specified": 1,
    "not_specified|Fanconi_anemia_complementation_group_L|Fanconi_anemia|FANCL-related_disorder": 1,
    "FANCL-related_disorder|Fanconi_anemia_complementation_group_L|Fanconi_anemia": 1,
    "FANCL-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_L": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_L|not_specified|FANCL-related_disorder": 1,
    "Fanconi_anemia_complementation_group_L|not_specified|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_L|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_L": 1,
    "Fanconi_anemia_complementation_group_L|not_specified|not_provided": 1,
    "FANCL-related_disorder|not_provided|Fanconi_anemia_complementation_group_L": 1,
    "FANCL-related_disorder|Fanconi_anemia_complementation_group_L": 1,
    "Dias-Logan_syndrome": 50,
    "Dias-Logan_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Dias-Logan_syndrome": 3,
    "Inborn_genetic_diseases|BCL11A-related_disorder": 1,
    "not_provided|Dias-Logan_syndrome": 5,
    "BCL11A-related_disorder": 12,
    "Dias-Logan_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|BCL11A-related_disorder": 3,
    "BCL11A-related_intellectual_disability|not_specified": 1,
    "Dias-Logan_syndrome|Intellectual_disability|_autosomal_dominant_45": 2,
    "Congenital_cerebellar_hypoplasia|Dias-Logan_syndrome": 1,
    "BCL11A-related_disorder|not_provided": 2,
    "BCL11A-related_BAFopathy": 3,
    "Dias-Logan_syndrome|See_cases|Neurodevelopmental_delay|not_provided": 1,
    "Dias-Logan_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Dias-Logan_syndrome|Fetal_hemoglobin_quantitative_trait_locus_5|not_specified|not_provided": 1,
    "Dias-Logan_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_cerebellar_hypoplasia|Cerebellar_vermis_hypoplasia|Corpus_callosum|_agenesis_of|Dias-Logan_syndrome": 1,
    "Dias-Logan_syndrome|Marfanoid_habitus_and_intellectual_disability": 1,
    "Postaxial_polydactyly|Delayed_speech_and_language_development": 1,
    "Neurodevelopmental_delay|Dias-Logan_syndrome": 1,
    "not_provided|REL-related_disorder": 1,
    "Immunodeficiency_92": 5,
    "REL-related_disorder": 1,
    "not_provided|Immunodeficiency_92": 2,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)": 421,
    "not_specified|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 3,
    "PEX13-related_disorder|not_specified|not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided": 14,
    "PEX13-related_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 13,
    "not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 14,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Inborn_genetic_diseases": 14,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided": 2,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Peroxisome_biogenesis_disorder_11B": 4,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Peroxisome_biogenesis_disorder_11B|Inborn_genetic_diseases|not_provided|PEX13-related_disorder": 1,
    "PEX13-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 1,
    "PEX13-related_disorder": 7,
    "not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_specified|PEX13-related_disorder": 1,
    "PEX13-related_disorder|not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 3,
    "PEX13-related_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 7,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 1,
    "PEX13-related_disorder|not_specified|Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_11B": 1,
    "not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)|Inborn_genetic_diseases": 1,
    "PEX13-related_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|PEX13-related_disorder": 6,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PEX13-related_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 2,
    "not_specified|Peroxisome_biogenesis_disorder_11A_(Zellweger)|PEX13-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder_11A_(Zellweger)|PEX13-related_disorder": 2,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided": 1,
    "PEX13-related_disorder|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|Peroxisome_biogenesis_disorder_11B|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_specified|not_provided": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_11B": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_11A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)|Peroxisome_biogenesis_disorder_11B|not_provided": 2,
    "PEX13-related_disorder|not_specified|Peroxisome_biogenesis_disorder_11A_(Zellweger)|Peroxisome_biogenesis_disorder_11B": 1,
    "Peroxisome_biogenesis_disorder_11B": 1,
    "Peroxisome_biogenesis_disorder_11A_(Zellweger)|PEX13-related_disorder|Inborn_genetic_diseases": 1,
    "PEX13-related_disorder|not_provided": 1,
    "PEX13-related_disorder|Peroxisome_biogenesis_disorder_11A_(Zellweger)|Inborn_genetic_diseases|not_provided": 1,
    "Chromosome_2p16.1-p15_deletion_syndrome": 1,
    "XPO1-associated_Neurodevelopmental_Disorder": 16,
    "not_provided|XPO1-associated_Neurodevelopmental_Disorder": 4,
    "XPO1-associated_Neurodevelopmental_Disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_28|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_28": 85,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|Retinal_dystrophy|FAM161A-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_28|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_28|Inborn_genetic_diseases": 4,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_28": 3,
    "not_provided|Retinitis_pigmentosa_28": 34,
    "Retinitis_pigmentosa_28|not_provided": 31,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_28|not_provided": 4,
    "Retinitis_pigmentosa_28|Inborn_genetic_diseases": 2,
    "FAM161A-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_28|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_28": 4,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_28|not_provided": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_28": 2,
    "FAM161A-related_disorder|Retinitis_pigmentosa_28|not_provided": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_28": 3,
    "Retinal_dystrophy|Inborn_genetic_diseases|Retinitis_pigmentosa_28|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_28|FAM161A-related_disorder": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_28": 3,
    "not_provided|FAM161A-related_disorder|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_28|FAM161A-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_28|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_28|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_28|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_28": 3,
    "Retinitis_pigmentosa|not_provided|Inborn_genetic_diseases": 8,
    "Retinitis_pigmentosa_28|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_28|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy|Retinitis_pigmentosa_28": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_28|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_28|Inborn_genetic_diseases|not_provided": 6,
    "Retinitis_pigmentosa_28|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|not_specified|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_28": 1,
    "not_provided|Retinitis_pigmentosa_28|Retinitis_pigmentosa": 3,
    "FAM161A-related_disorder|Retinitis_pigmentosa_28|not_provided|Retinitis_pigmentosa": 1,
    "FAM161A-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_28": 1,
    "Retinitis_pigmentosa_28|Retinal_dystrophy": 2,
    "not_specified|Retinitis_pigmentosa_28": 2,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_28|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_28|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_28": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_28": 2,
    "FAM161A-related_disorder": 1,
    "Retinitis_pigmentosa_28|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_28|not_provided|Retinal_dystrophy": 1,
    "FAM161A-related_disorder|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "not_provided|Inborn_genetic_diseases|FAM161A-related_disorder|Retinitis_pigmentosa_28": 1,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_28": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_28|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_28|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "FAM161A-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_28|FAM161A-related_disorder|not_provided": 1,
    "not_specified|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_28": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_28|not_specified": 1,
    "Retinitis_pigmentosa_28|not_specified|not_provided": 1,
    "not_specified|CCT4-related_disorder": 1,
    "CCT4-related_disorder": 1,
    "B3GNT2-related_disorder": 3,
    "not_provided|B3GNT2-related_disorder": 1,
    "Orofaciodigital_syndrome_I": 39,
    "Meckel-Gruber_syndrome|not_specified": 2,
    "EHBP1-related_disorder": 7,
    "Prostate_cancer|_hereditary|_12|EHBP1-related_disorder": 1,
    "not_provided|EHBP1-related_disorder": 1,
    "OTX1-related_disorder|not_provided": 1,
    "not_provided|OTX1-related_disorder": 1,
    "Bardet-Biedl_syndrome_15": 20,
    "not_provided|Bardet-Biedl_syndrome_15": 4,
    "WDPCP-related_disorder": 81,
    "Bardet-Biedl_syndrome_15|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder": 15,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome": 18,
    "WDPCP-related_disorder|Inborn_genetic_diseases|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15": 3,
    "Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome": 7,
    "WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome": 2,
    "not_provided|WDPCP-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15": 13,
    "Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 41,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 2,
    "Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome": 13,
    "WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15": 5,
    "Bardet-Biedl_syndrome_15|Inborn_genetic_diseases|Bardet-Biedl_syndrome|WDPCP-related_disorder": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 5,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|WDPCP-related_disorder": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_15": 1,
    "Bardet-Biedl_syndrome|not_provided": 35,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|WDPCP-related_disorder": 5,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases": 54,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 7,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome": 22,
    "not_provided|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|not_specified": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_1|not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15": 1,
    "Inborn_genetic_diseases|WDPCP-related_disorder": 4,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|WDPCP-related_disorder|Inborn_genetic_diseases": 1,
    "Optic_atrophy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|WDPCP-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 4,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|not_provided|Bardet-Biedl_syndrome_15": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases|not_provided": 1,
    "WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome|WDPCP-related_disorder": 1,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_15|WDPCP-related_disorder|Bardet-Biedl_syndrome": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 1,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome|not_specified": 1,
    "Bardet-Biedl_syndrome|Retinal_dystrophy": 12,
    "not_provided|Bardet-Biedl_syndrome": 46,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15": 2,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases|Bardet-Biedl_syndrome|WDPCP-related_disorder": 1,
    "WDPCP-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|not_provided|WDPCP-related_disorder|Inborn_genetic_diseases": 1,
    "WDPCP-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 5,
    "Inborn_genetic_diseases|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|WDPCP-related_disorder": 3,
    "not_specified|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|not_provided|Joubert_syndrome|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder": 2,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 2,
    "WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|not_provided|Bardet-Biedl_syndrome": 1,
    "WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases": 1,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|WDPCP-related_disorder": 2,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|WDPCP-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|not_provided": 1,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome|WDPCP-related_disorder": 4,
    "Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder": 2,
    "not_provided|Bardet-Biedl_syndrome|WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_12|_modifier_of": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Orofaciodigital_syndrome": 1,
    "Bardet-Biedl_syndrome|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome": 56,
    "not_specified|Bardet-Biedl_syndrome|not_provided": 3,
    "not_provided|Bardet-Biedl_syndrome|not_specified": 2,
    "WDPCP-related_disorder|Bardet-Biedl_syndrome|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15": 1,
    "Bardet-Biedl_syndrome_15|WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|not_provided|Bardet-Biedl_syndrome": 1,
    "Optic_atrophy|WDPCP-related_disorder": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Inborn_genetic_diseases|WDPCP-related_disorder|Bardet-Biedl_syndrome": 1,
    "Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome|WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome": 1,
    "Meckel_syndrome|_type_6|_modifier_of": 1,
    "Orofaciodigital_syndrome|Bardet-Biedl_syndrome|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|WDPCP-related_disorder|Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_15|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome|WDPCP-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_15|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|WDPCP-related_disorder|Bardet-Biedl_syndrome": 1,
    "WDPCP-related_disorder|Heart_defect_-_tongue_hamartoma_-_polysyndactyly_syndrome|Bardet-Biedl_syndrome_15|Bardet-Biedl_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_15|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_88": 1,
    "Developmental_and_epileptic_encephalopathy|_83": 6,
    "Developmental_and_epileptic_encephalopathy|_83|D-6618|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_83": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_83": 1,
    "UGP2-related_disorder": 3,
    "Large_for_gestational_age": 15,
    "Spastic_tetraplegia-thin_corpus_callosum-progressive_postnatal_microcephaly_syndrome": 20,
    "SLC1A4-related_disorder|not_provided": 5,
    "Spastic_tetraplegia-thin_corpus_callosum-progressive_postnatal_microcephaly_syndrome|not_provided": 4,
    "SLC1A4-related_disorder": 3,
    "not_provided|Spastic_tetraplegia-thin_corpus_callosum-progressive_postnatal_microcephaly_syndrome": 4,
    "not_provided|Spastic_tetraplegia-thin_corpus_callosum-progressive_postnatal_microcephaly_syndrome|Inborn_genetic_diseases": 1,
    "SLC1A4-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spastic_tetraplegia-thin_corpus_callosum-progressive_postnatal_microcephaly_syndrome": 1,
    "not_specified|not_provided|Spastic_tetraplegia-thin_corpus_callosum-progressive_postnatal_microcephaly_syndrome": 1,
    "not_provided|SLC1A4-related_disorder": 1,
    "Noonan_syndrome_14|Noonan_syndrome": 2,
    "Severe_postnatal_growth_retardation": 1,
    "Noonan_syndrome|Noonan_syndrome_14": 1,
    "Noonan_syndrome_14": 1,
    "MEIS1-related_disorder": 2,
    "not_specified|Aganglionic_megacolon": 1,
    "ARHGAP25-related_condition": 2,
    "not_provided|Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 2,
    "ANTXR1-related_disorder|not_provided": 3,
    "not_provided|ANTXR1-related_disorder": 2,
    "not_provided|GAPO_syndrome|Inborn_genetic_diseases": 1,
    "GAPO_syndrome": 10,
    "not_provided|GAPO_syndrome": 7,
    "GAPO_syndrome|not_provided": 9,
    "ANTXR1-related_disorder": 6,
    "GAPO_syndrome|Inborn_genetic_diseases": 1,
    "Capillary_infantile_hemangioma": 10,
    "Inborn_genetic_diseases|GAPO_syndrome": 1,
    "not_provided|not_specified|GAPO_syndrome|Capillary_infantile_hemangioma": 1,
    "Bladder_exstrophy-epispadias-cloacal_extrophy_complex|Inborn_genetic_diseases": 1,
    "ANTXR1-related_disorder|GAPO_syndrome": 1,
    "not_provided|Capillary_infantile_hemangioma": 1,
    "Congenital_myasthenic_syndrome_12": 418,
    "Congenital_myasthenic_syndrome_12|not_provided": 22,
    "Congenital_Myasthenic_Syndrome|_Recessive": 13,
    "not_provided|Congenital_Myasthenic_Syndrome|_Recessive": 5,
    "not_provided|Congenital_myasthenic_syndrome_12": 6,
    "Congenital_myasthenic_syndrome|not_specified|not_provided|Congenital_myasthenic_syndrome_12": 1,
    "Congenital_myasthenic_syndrome_12|not_provided|not_specified|Congenital_Myasthenic_Syndrome|_Recessive": 1,
    "Congenital_myasthenic_syndrome_12|Congenital_Myasthenic_Syndrome|_Recessive|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_12": 5,
    "Congenital_myasthenic_syndrome_12|GFPT1-related_disorder": 1,
    "Congenital_myasthenic_syndrome_12|not_specified": 7,
    "Congenital_myasthenic_syndrome_12|GFPT1-related_disorder|Congenital_myasthenic_syndrome_4C": 1,
    "not_specified|Congenital_myasthenic_syndrome_12": 5,
    "not_provided|Congenital_myasthenic_syndrome_13|Congenital_myasthenic_syndrome_12|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_12|Hereditary_ataxia": 1,
    "Congenital_myasthenic_syndrome_12|not_provided|Congenital_Myasthenic_Syndrome|_Recessive|not_specified": 1,
    "GFPT1-related_myopathy_with_protein_aggregates_and_rimmed_vacuoles|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_12": 1,
    "GFPT1-related_disorder|Congenital_myasthenic_syndrome_12": 3,
    "not_specified|Congenital_myasthenic_syndrome_12|not_provided": 2,
    "Congenital_myasthenic_syndrome_12|Inborn_genetic_diseases": 6,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_12": 3,
    "GFPT1-related_disorder|Congenital_myasthenic_syndrome_12|not_provided|GFPT1-related_myasthenic_syndrome|Congenital_myasthenic_syndrome_4C|Abnormality_of_the_musculature": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_12|GFPT1-related_disorder": 1,
    "Congenital_myasthenic_syndrome_12|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_12|not_provided": 1,
    "Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_12": 1,
    "not_provided|Congenital_myasthenic_syndrome_12|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_12|not_provided|not_specified": 2,
    "Congenital_myasthenic_syndrome_12|GFPT1-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_12": 1,
    "Congenital_myasthenic_syndrome_4C|not_provided": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_1": 78,
    "Spastic_paraplegia_93|_autosomal_recessive": 4,
    "Multiple_mitochondrial_dysfunctions_syndrome_1|not_provided": 7,
    "Multiple_mitochondrial_dysfunctions_syndrome_1|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Multiple_mitochondrial_dysfunctions_syndrome_1": 2,
    "Spastic_paraplegia_93|_autosomal_recessive|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "NFU1-related_disorder|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "Spastic_paraplegia_93|_autosomal_recessive|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "Spastic_paraplegia_93|_autosomal_recessive|not_provided": 4,
    "NFU1-related_disorder": 3,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1": 8,
    "Multiple_mitochondrial_dysfunctions_syndrome_1|NFU1-related_disorder": 3,
    "NFU1-related_disorder|not_specified|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "Inborn_genetic_diseases|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "Fatal_multiple_mitochondrial_dysfunctions_syndrome|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "not_specified|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "not_specified|Multiple_mitochondrial_dysfunctions_syndrome_1|not_provided": 2,
    "not_specified|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1": 1,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_1|not_specified": 1,
    "Fatal_multiple_mitochondrial_dysfunctions_syndrome": 1,
    "Autosomal_dominant_lamellar_ichthyosis": 4,
    "Inborn_genetic_diseases|Prostate_cancer": 2,
    "Welander_distal_myopathy": 200,
    "not_provided|Welander_distal_myopathy": 12,
    "Amyotrophic_lateral_sclerosis_26_with_or_without_frontotemporal_dementia|Welander_distal_myopathy": 1,
    "Welander_distal_myopathy|not_provided": 10,
    "not_specified|not_provided|Welander_distal_myopathy": 1,
    "not_provided|Welander_distal_myopathy|AMYOTROPHIC_LATERAL_SCLEROSIS_26_WITH_FRONTOTEMPORAL_DEMENTIA": 1,
    "TIA1-related_disorder|Amyotrophic_lateral_sclerosis_26_with_or_without_frontotemporal_dementia|not_specified|not_provided|Welander_distal_myopathy": 1,
    "Welander_distal_myopathy|Inborn_genetic_diseases": 4,
    "not_specified|Welander_distal_myopathy|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_26_with_or_without_frontotemporal_dementia": 2,
    "not_provided|Welander_distal_myopathy|Inborn_genetic_diseases": 1,
    "not_provided|Welander_distal_myopathy|not_specified": 1,
    "Welander_distal_myopathy|Amyotrophic_lateral_sclerosis_26_with_or_without_frontotemporal_dementia": 1,
    "Inborn_genetic_diseases|Welander_distal_myopathy": 1,
    "Welander_distal_myopathy|not_provided|not_specified": 1,
    "Welander_distal_myopathy|not_specified": 1,
    "not_specified|Welander_distal_myopathy|TIA1-related_disorder": 1,
    "Welander_distal_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "TIA1-related_disorder|Welander_distal_myopathy": 1,
    "Welander_distal_myopathy|not_specified|not_provided": 1,
    "FAM136A-related_disorder": 11,
    "not_specified|FAM136A-related_disorder": 1,
    "Premature_ovarian_failure_6|not_provided": 5,
    "Premature_ovarian_failure_6|FIGLA-related_condition|not_provided|not_specified": 1,
    "Premature_ovarian_failure_6|FIGLA-related_condition|not_specified|not_provided": 1,
    "Premature_ovarian_failure_6|FIGLA-related_condition": 1,
    "Premature_ovarian_failure_6": 15,
    "Premature_ovarian_failure_6|Inborn_genetic_diseases": 3,
    "Premature_ovarian_failure_6|Genetic_non-acquired_premature_ovarian_failure": 2,
    "Inborn_genetic_diseases|Premature_ovarian_failure_6": 1,
    "Inborn_genetic_diseases|not_specified|Premature_ovarian_failure_6": 1,
    "CD207-related_disorder": 9,
    "not_provided|Birbeck_granule_deficiency": 1,
    "Birbeck_granule_deficiency": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided": 48,
    "not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_specified": 6,
    "not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 39,
    "ATP6V1B1-related_disorder|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness": 128,
    "not_provided|Inborn_genetic_diseases|Renal_tubular_acidosis_with_progressive_nerve_deafness": 2,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|not_specified": 2,
    "not_provided|not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness": 4,
    "not_specified|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 6,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|Inborn_genetic_diseases": 8,
    "not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided|ATP6V1B1-related_disorder": 2,
    "not_provided|Renal_tubular_acidosis": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|ATP6V1B1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hearing_impairment|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided": 1,
    "not_provided|ATP6V1B1-related_disorder|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_specified": 1,
    "not_provided|ATP6V1B1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 3,
    "ATP6V1B1-related_disorder|Polydactyly|_postaxial|_type_A1|Nephrocalcinosis|not_provided": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided|not_specified": 3,
    "not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness|ATP6V1B1-related_disorder|not_provided": 1,
    "Nephrocalcinosis|Nephrolithiasis|Distal_renal_tubular_acidosis|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 1,
    "not_provided|not_specified|ATP6V1B1-related_disorder|Renal_tubular_acidosis_with_progressive_nerve_deafness": 1,
    "not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness|ATP6V1B1-related_disorder": 2,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided|not_specified|Inborn_genetic_diseases": 2,
    "not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness": 2,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided|Inborn_genetic_diseases": 3,
    "not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided": 4,
    "Hearing_impairment|not_specified|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 2,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|not_specified|not_provided": 2,
    "Distal_renal_tubular_acidosis|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 2,
    "Abnormality_of_the_genitourinary_system": 1,
    "ATP6V1B1-related_disorder": 1,
    "not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Renal_tubular_acidosis_with_progressive_nerve_deafness|Inborn_genetic_diseases|not_provided": 1,
    "Rare_genetic_deafness|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|Inborn_genetic_diseases|not_provided": 1,
    "ATP6V1B1-related_disorder|not_specified|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 1,
    "ATP6V1B1-related_disorder|not_provided": 3,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|ATP6V1B1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Renal_tubular_acidosis|Renal_tubular_acidosis_with_progressive_nerve_deafness|not_provided": 1,
    "not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness|Inborn_genetic_diseases": 1,
    "ATP6V1B1-related_disorder|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness": 2,
    "not_specified|not_provided|Renal_tubular_acidosis_with_progressive_nerve_deafness|ATP6V1B1-related_disorder": 1,
    "not_provided|ATP6V1B1-related_disorder|Renal_tubular_acidosis_with_progressive_nerve_deafness": 2,
    "Methylmalonic_acidemia|not_provided": 17,
    "not_provided|Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency": 3,
    "Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency": 78,
    "Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency": 4,
    "Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency|MCEE-related_disorder": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency": 3,
    "Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency|not_specified": 1,
    "Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency|not_provided|not_specified": 2,
    "MCEE-related_disorder|Inborn_genetic_diseases|not_provided|Methylmalonic_acidemia|Methylmalonic_acidemia_due_to_methylmalonyl-CoA_epimerase_deficiency": 1,
    "Methylmalonic_acidemia": 56,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 100,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2079,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 137,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 210,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 99,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 9,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 29,
    "Miyoshi_muscular_dystrophy_1|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Miyoshi_muscular_dystrophy_1": 58,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 72,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 9,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset": 44,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 8,
    "Miyoshi_muscular_dystrophy_1|not_provided": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy": 31,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 17,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 9,
    "DYSF-related_disorder|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 32,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 18,
    "Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 5,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset": 3,
    "not_provided|Miyoshi_muscular_dystrophy_1": 20,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 15,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Abnormality_of_the_musculature|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 7,
    "Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 34,
    "Miyoshi_myopathy|not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified": 1,
    "Muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 45,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 11,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 6,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 6,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Inborn_genetic_diseases": 4,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 8,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 6,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Limb-girdle_muscular_dystrophy|_recessive": 14,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|not_provided": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "not_provided|DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "DYSF-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 5,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|not_provided": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified": 10,
    "Limb-girdle_muscular_dystrophy|_recessive|Inborn_genetic_diseases|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 14,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|not_specified": 1,
    "DYSF-related_disorder": 10,
    "Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases": 20,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|not_specified": 1,
    "DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 10,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_myopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 13,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1": 2,
    "not_provided|Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 5,
    "not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_myopathy|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|DYSF-related_disorder": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 5,
    "not_provided|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Abnormality_of_the_musculature": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|not_provided|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_myopathy|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|not_specified|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_myopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 2,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 6,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_myopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder": 1,
    "Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 13,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified|DYSF-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 3,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Limb-girdle_muscular_dystrophy|_recessive": 4,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_provided|DYSF-related_disorder": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 4,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "DYSF-related_disorder|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|DYSF-related_disorder|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_myopathy|Miyoshi_muscular_dystrophy_1|Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_specified|not_provided|DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|not_provided": 5,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Peripheral_neuropathy|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|DYSF-related_disorder|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive": 5,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Miyoshi_myopathy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases": 4,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1": 4,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 3,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Miyoshi_muscular_dystrophy_1|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 5,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "not_specified|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "DYSF-related_disorder|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 3,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Limb-girdle_muscular_dystrophy|_recessive|DYSF-related_disorder|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_myopathy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Inborn_genetic_diseases|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset": 3,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Miyoshi_myopathy|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|DYSF-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 4,
    "Inborn_genetic_diseases|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 4,
    "Muscle_weakness|Arthralgia|Myalgia|EMG:_myopathic_abnormalities|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "DYSF-related_disorder|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Absent_muscle_fiber_dysferlin|Foot_dorsiflexor_weakness|Peroneal_muscle_atrophy|Distal_lower_limb_muscle_weakness": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Inborn_genetic_diseases|not_provided|Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases": 3,
    "Miyoshi_muscular_dystrophy_1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified": 1,
    "not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "See_cases|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "DYSF-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 4,
    "not_provided|DYSF-related_disorder": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|DYSF-related_disorder|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|DYSF-related_disorder|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|DYSF-related_disorder|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 3,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 3,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 2,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Inborn_genetic_diseases": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Abnormality_of_the_musculature|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|not_provided": 1,
    "DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Miyoshi_muscular_dystrophy_1": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Inborn_genetic_diseases|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases": 1,
    "Distal_myopathy_with_anterior_tibial_onset": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|DYSF-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 2,
    "DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|not_provided": 2,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 1,
    "not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Abnormality_of_the_musculature": 1,
    "DYSF-related_disorder|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Abnormality_of_the_musculature": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|DYSF-related_disorder|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified": 1,
    "DYSF-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 5,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Muscular_dystrophy": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "DYSF-related_disorder|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|not_specified|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|DYSF-related_disorder|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Inborn_genetic_diseases|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "DYSF-related_disorder|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 3,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|DYSF-related_disorder|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "DYSF-related_disorder|Miyoshi_myopathy|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 2,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|DYSF-related_disorder": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Inborn_genetic_diseases": 1,
    "Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_specified": 1,
    "not_provided|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|DYSF-related_disorder": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "See_cases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|not_specified": 1,
    "Miyoshi_muscular_dystrophy_1|Abnormality_of_the_musculature": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive|Inborn_genetic_diseases|not_provided|Miyoshi_myopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|not_specified": 1,
    "DYSF-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|DYSF-related_disorder|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Proximal_muscle_weakness": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|DYSF-related_disorder|not_provided": 1,
    "DYSF-related_disorder|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_specified|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|not_specified|not_provided": 1,
    "not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|not_provided": 2,
    "Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|not_specified|not_provided": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|DYSF-related_disorder": 1,
    "Inborn_genetic_diseases|DYSF-related_disorder|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|DYSF-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|not_provided": 2,
    "not_provided|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Distal_myopathy_with_anterior_tibial_onset|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "not_specified|not_provided|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 1,
    "Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Miyoshi_muscular_dystrophy_1|Distal_lower_limb_muscle_weakness": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1": 1,
    "DYSF-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Miyoshi_muscular_dystrophy_1|DYSF-related_disorder": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided": 1,
    "DYSF-related_disorder|not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|not_provided|DYSF-related_disorder|not_specified": 1,
    "Miyoshi_myopathy|DYSF-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Inborn_genetic_diseases|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "not_specified|Miyoshi_muscular_dystrophy_1|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Inborn_genetic_diseases|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Distal_myopathy_with_anterior_tibial_onset|Miyoshi_muscular_dystrophy_1|not_provided|Abnormality_of_the_musculature": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Miyoshi_muscular_dystrophy_1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2B|Miyoshi_muscular_dystrophy_1|Distal_myopathy_with_anterior_tibial_onset": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided|Miyoshi_myopathy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dysferlin": 1,
    "Inborn_genetic_diseases|CYP26B1-related_disorder|not_provided": 1,
    "Lethal_occipital_encephalocele-skeletal_dysplasia_syndrome": 4,
    "not_provided|CYP26B1-related_disorder": 5,
    "Lethal_occipital_encephalocele-skeletal_dysplasia_syndrome|not_provided": 1,
    "not_provided|Lethal_occipital_encephalocele-skeletal_dysplasia_syndrome": 2,
    "Lethal_occipital_encephalocele-skeletal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CYP26B1-related_disorder": 1,
    "Lethal_occipital_encephalocele-skeletal_dysplasia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "CYP26B1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|CYP26B1-related_disorder": 1,
    "not_provided|EXOC6B-related_disorder": 6,
    "EXOC6B-related_disorder": 6,
    "Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_3": 6,
    "EXOC6B-related_disorder|not_provided": 4,
    "not_provided|Spondyloepimetaphyseal_dysplasia_with_joint_laxity|_type_3": 1,
    "not_provided|Dystonic_disorder": 37,
    "Dopa-responsive_dystonia": 2,
    "Dystonic_disorder": 895,
    "not_provided|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 2,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|not_provided": 1,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 43,
    "Dystonic_disorder|Inborn_genetic_diseases": 14,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Dystonic_disorder": 4,
    "Dystonic_disorder|Inborn_genetic_diseases|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "Dystonic_disorder|not_provided": 48,
    "Dystonic_disorder|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 7,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Dystonic_disorder|Inborn_genetic_diseases": 1,
    "SPR-related_disorder|Dystonic_disorder|not_specified|not_provided|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "not_provided|Dystonic_disorder|Inborn_genetic_diseases|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Dystonic_disorder|not_provided": 3,
    "Dystonic_disorder|SPR-related_disorder": 2,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Inborn_genetic_diseases|Dystonic_disorder": 1,
    "not_provided|Dystonic_disorder|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "Intellectual_disability|Dystonic_disorder": 1,
    "Dystonic_disorder|not_provided|Inborn_genetic_diseases|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "Inborn_genetic_diseases|Dystonic_disorder": 16,
    "not_provided|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Dystonic_disorder": 2,
    "SPR-related_disorder|Dystonic_disorder|not_provided|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|not_specified|Dystonic_disorder": 1,
    "not_specified|not_provided|Dystonic_disorder": 2,
    "Dystonic_disorder|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency|Inborn_genetic_diseases": 1,
    "Dystonic_disorder|not_provided|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 2,
    "SPR-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Dystonic_disorder|Dopa-responsive_dystonia_due_to_sepiapterin_reductase_deficiency": 1,
    "SPR-related_disorder|Dystonic_disorder": 1,
    "RAB11FIP5-related_disorder": 10,
    "RAB11FIP5-related_disorder|not_provided": 1,
    "not_provided|RAB11FIP5-related_disorder": 2,
    "Alstrom_syndrome": 4031,
    "Alstrom_syndrome|not_specified|ALMS1-related_disorder|Cardiovascular_phenotype": 2,
    "Alstrom_syndrome|Cardiovascular_phenotype": 405,
    "Cardiovascular_phenotype|not_provided|Alstrom_syndrome": 70,
    "Cardiovascular_phenotype|Alstrom_syndrome": 492,
    "Cardiovascular_phenotype|ALMS1-related_disorder": 3,
    "not_provided|not_specified|Alstrom_syndrome": 3,
    "not_specified|Alstrom_syndrome|not_provided|Cardiovascular_phenotype": 7,
    "Cardiovascular_phenotype|not_specified|not_provided|Alstrom_syndrome": 16,
    "Cardiovascular_phenotype|Alstrom_syndrome|not_specified": 18,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_specified": 15,
    "not_specified|Alstrom_syndrome|ALMS1-related_disorder": 2,
    "Alstrom_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 4,
    "Alstrom_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 9,
    "ALMS1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "ALMS1-related_disorder": 194,
    "Alstrom_syndrome|not_provided|Retinal_dystrophy": 1,
    "not_specified|not_provided|Alstrom_syndrome|Cardiovascular_phenotype": 16,
    "Alstrom_syndrome|not_specified|not_provided": 5,
    "Alstrom_syndrome|not_specified": 33,
    "not_specified|Cardiovascular_phenotype|Alstrom_syndrome": 12,
    "not_provided|Alstrom_syndrome": 98,
    "Alstrom_syndrome|not_provided": 89,
    "ALMS1-related_disorder|Alstrom_syndrome": 29,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_provided": 61,
    "not_provided|ALMS1-related_disorder|Cardiovascular_phenotype|Alstrom_syndrome": 1,
    "Alstrom_syndrome|not_provided|Cardiovascular_phenotype|not_specified": 6,
    "Alstrom_syndrome|not_provided|Cardiovascular_phenotype": 47,
    "Alstrom_syndrome|ALMS1-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Alstrom_syndrome": 48,
    "not_provided|Alstrom_syndrome|Cardiovascular_phenotype": 69,
    "Alstrom_syndrome|ALMS1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|ALMS1-related_disorder|Alstrom_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Alstrom_syndrome|not_provided": 7,
    "not_provided|not_specified|Cardiovascular_phenotype|Alstrom_syndrome": 6,
    "Alstrom_syndrome|ALMS1-related_disorder": 12,
    "Cardiovascular_phenotype|Alstrom_syndrome|Retinal_dystrophy": 2,
    "not_provided|Retinal_dystrophy|Alstrom_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Alstrom_syndrome|Retinal_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|Alstrom_syndrome|ALMS1-related_disorder": 1,
    "ALMS1-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Alstrom_syndrome|not_provided": 52,
    "not_provided|Alstrom_syndrome|Cardiovascular_phenotype|ALMS1-related_disorder": 1,
    "ALMS1-related_disorder|not_provided|Alstrom_syndrome": 2,
    "Cardiovascular_phenotype|Alstrom_syndrome|not_specified|not_provided": 8,
    "Cardiovascular_phenotype|ALMS1-related_disorder|not_specified|Alstrom_syndrome": 1,
    "Alstrom_syndrome|Monogenic_diabetes|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Monogenic_diabetes|Alstrom_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Alstrom_syndrome": 26,
    "not_specified|Alstrom_syndrome": 48,
    "not_specified|Alstrom_syndrome|not_provided|Cardiovascular_phenotype|Monogenic_diabetes": 1,
    "Cardiovascular_phenotype|not_provided|Alstrom_syndrome|not_specified": 10,
    "Alstrom_syndrome|not_provided|not_specified": 9,
    "Alstrom_syndrome|not_provided|Cone-rod_dystrophy": 1,
    "Alstrom_syndrome|Retinitis_pigmentosa": 1,
    "Alstrom_syndrome|Retinal_dystrophy": 9,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 12,
    "Monogenic_diabetes|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Alstrom_syndrome": 5,
    "Retinal_dystrophy|Cardiovascular_phenotype|Alstrom_syndrome": 1,
    "Monogenic_diabetes|Cardiovascular_phenotype|not_specified|not_provided|Alstrom_syndrome": 3,
    "not_provided|Alstrom_syndrome|Cardiovascular_phenotype|not_specified": 6,
    "not_provided|Cardiovascular_phenotype|Alstrom_syndrome|not_specified": 8,
    "Cardiovascular_phenotype|Alstrom_syndrome|ALMS1-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Cardiovascular_phenotype|ALMS1-related_disorder|not_provided|Alstrom_syndrome": 1,
    "Retinal_dystrophy|_early-onset_severe": 3,
    "Occult_maculopathy|Alstrom_syndrome": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Monogenic_diabetes|Alstrom_syndrome|Hearing_impairment|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Alstrom_syndrome": 1,
    "not_provided|Alstrom_syndrome|not_specified|Cardiovascular_phenotype": 4,
    "Alstrom_syndrome|not_specified|Cardiovascular_phenotype": 10,
    "not_provided|Monogenic_diabetes|Retinal_dystrophy|Alstrom_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 10,
    "not_provided|Cardiovascular_phenotype|Alstrom_syndrome|Leukodystrophy|Stage_5_chronic_kidney_disease|Visual_impairment|Hearing_impairment": 1,
    "Retinal_dystrophy|Alstrom_syndrome|not_provided": 1,
    "Alstrom_syndrome|Monogenic_diabetes|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_provided|Monogenic_diabetes|not_specified": 2,
    "Cardiomyopathy|not_provided|Alstrom_syndrome": 1,
    "Cardiovascular_phenotype|Monogenic_diabetes|not_specified|not_provided|Alstrom_syndrome": 7,
    "Cardiovascular_phenotype|not_provided|not_specified|Alstrom_syndrome": 4,
    "Cardiovascular_phenotype|ALMS1-related_disorder|Alstrom_syndrome": 4,
    "Alstrom_syndrome|Cardiovascular_phenotype|Retinal_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Alstrom_syndrome|ALMS1-related_disorder": 3,
    "ALMS1-related_disorder|Cardiovascular_phenotype": 3,
    "ALMS1-related_disorder|Alstrom_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Alstrom_syndrome|not_provided|not_specified": 3,
    "not_specified|not_provided|Cardiovascular_phenotype|Alstrom_syndrome": 10,
    "Cardiovascular_phenotype|not_specified|Alstrom_syndrome|not_provided": 10,
    "not_specified|Alstrom_syndrome|Cardiovascular_phenotype": 8,
    "Alstrom_syndrome|Monogenic_diabetes|Cardiovascular_phenotype": 2,
    "Leber_congenital_amaurosis|Alstrom_syndrome": 2,
    "not_provided|Alstrom_syndrome|Cardiovascular_phenotype|not_specified|Monogenic_diabetes": 1,
    "ALMS1-related_disorder|Cardiovascular_phenotype|Alstrom_syndrome": 3,
    "not_provided|not_specified|Alstrom_syndrome|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Monogenic_diabetes|not_specified|Alstrom_syndrome|not_provided": 1,
    "not_provided|Alstrom_syndrome|Cardiovascular_phenotype|Retinal_dystrophy": 2,
    "ALMS1-related_disorder|Cardiovascular_phenotype|Alstrom_syndrome|not_specified": 2,
    "not_provided|Alstrom_syndrome|Monogenic_diabetes|Cardiovascular_phenotype": 2,
    "Alstrom_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 5,
    "ALMS1-related_disorder|Alstrom_syndrome|not_specified": 1,
    "not_provided|Retinal_dystrophy|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Alstrom_syndrome": 5,
    "Retinal_dystrophy|not_provided|Alstrom_syndrome": 1,
    "not_specified|not_provided|Alstrom_syndrome|Cardiovascular_phenotype|Monogenic_diabetes": 2,
    "Monogenic_diabetes|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "Retinal_dystrophy|not_provided|Cardiovascular_phenotype|Alstrom_syndrome": 1,
    "Monogenic_diabetes|not_specified|not_provided|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Alstrom_syndrome|not_provided|Retinal_dystrophy": 1,
    "Cardiovascular_phenotype|Monogenic_diabetes|not_provided|Alstrom_syndrome": 1,
    "Monogenic_diabetes|Cardiovascular_phenotype|Alstrom_syndrome|not_provided|not_specified": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Monogenic_diabetes": 2,
    "Intellectual_disability|Alstrom_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Monogenic_diabetes|Alstrom_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Retinal_dystrophy|_early-onset_severe|Alstrom_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Retinal_dystrophy|Alstrom_syndrome": 1,
    "not_specified|ALMS1-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Alstrom_syndrome|Retinal_dystrophy|not_provided": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|ALMS1-related_disorder": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Alstrom_syndrome|Monogenic_diabetes": 1,
    "Cardiovascular_phenotype|Alstrom_syndrome|Retinal_dystrophy|not_provided": 3,
    "Cardiovascular_phenotype|Hearing_impairment|Alstrom_syndrome": 1,
    "Alstrom_syndrome|not_provided|Cardiovascular_phenotype|not_specified|Monogenic_diabetes": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|ALMS1-related_disorder|not_provided": 1,
    "not_provided|Monogenic_diabetes|Cardiovascular_phenotype|not_specified|Alstrom_syndrome": 1,
    "Retinal_dystrophy|Alstrom_syndrome|Monogenic_diabetes|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Monogenic_diabetes|Alstrom_syndrome": 1,
    "ALMS1-related_disorder|Alstrom_syndrome|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Monogenic_diabetes|Alstrom_syndrome": 1,
    "Optic_atrophy|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "Alstrom_syndrome|not_provided|Cardiovascular_phenotype|Monogenic_diabetes|not_specified": 2,
    "Monogenic_diabetes|Alstrom_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Monogenic_diabetes|Alstrom_syndrome": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Alstrom_syndrome|not_provided": 1,
    "Monogenic_diabetes|not_specified|Alstrom_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Retinal_dystrophy|Alstrom_syndrome|not_specified": 1,
    "Alstrom_syndrome|not_specified|Cardiovascular_phenotype|not_provided|Monogenic_diabetes": 1,
    "not_provided|Alstrom_syndrome|Stickler_syndrome": 1,
    "Intellectual_disability|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Alstrom_syndrome": 2,
    "Monogenic_diabetes|Alstrom_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Alstrom_syndrome|Retinal_dystrophy|not_provided": 2,
    "Alstrom_syndrome|not_provided|Cardiovascular_phenotype|ALMS1-related_disorder|not_specified": 1,
    "ALMS1-related_disorder|Cardiovascular_phenotype|not_provided|Alstrom_syndrome": 1,
    "Nephrotic_syndrome|not_provided|Alstrom_syndrome": 1,
    "Retinal_dystrophy|not_provided|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "Monogenic_diabetes|Alstrom_syndrome": 2,
    "Alstr\u00f6m_Syndrom": 1,
    "Cardiovascular_phenotype|not_provided|Down_syndrome|Alstrom_syndrome": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|Retinal_dystrophy": 1,
    "Alstrom_syndrome|Retinal_dystrophy|Cardiovascular_phenotype": 1,
    "Retinal_dystrophy|Alstrom_syndrome": 8,
    "not_specified|ALMS1-related_disorder|Cardiovascular_phenotype|not_provided|Alstrom_syndrome": 1,
    "Alstrom_syndrome|not_provided|Cardiovascular_phenotype|Retinal_dystrophy": 1,
    "not_provided|Nephrotic_syndrome|Alstrom_syndrome": 1,
    "Alstrom_syndrome|Monogenic_diabetes": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_specified|Alstrom_syndrome|not_provided": 3,
    "Cardiovascular_phenotype|not_provided|Hearing_impairment|not_specified|Alstrom_syndrome": 1,
    "Hearing_impairment|Cardiovascular_phenotype|Alstrom_syndrome": 1,
    "not_specified|Alstrom_syndrome|Cardiovascular_phenotype|Monogenic_diabetes|not_provided": 1,
    "Monogenic_diabetes|Cardiovascular_phenotype|not_provided|not_specified|Alstrom_syndrome": 1,
    "Alstrom_syndrome|ALMS1-related_disorder|not_provided": 1,
    "Alstrom_syndrome|Bardet-Biedl_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Alstrom_syndrome|Monogenic_diabetes|not_provided": 1,
    "Alstrom_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Monogenic_diabetes": 2,
    "Cardiovascular_phenotype|Alstrom_syndrome|not_provided|Retinal_dystrophy": 1,
    "Cardiovascular_phenotype|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Alstrom_syndrome": 1,
    "ALMS1-related_disorder|Cardiovascular_phenotype|not_provided|Alstrom_syndrome|not_specified": 1,
    "Retinal_dystrophy|Alstrom_syndrome|Cardiovascular_phenotype": 1,
    "Alstrom_syndrome|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome": 1,
    "Alstrom_syndrome|Monogenic_diabetes|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Retinal_dystrophy|ALMS1-related_disorder|Alstrom_syndrome": 1,
    "Alstrom_syndrome|Bardet-Biedl_syndrome|Cardiovascular_phenotype": 1,
    "Monogenic_diabetes|Cardiovascular_phenotype|not_provided|Alstrom_syndrome": 1,
    "Alstrom_syndrome|ALMS1-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Monogenic_diabetes": 1,
    "Alstrom_syndrome|Retinal_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Alstrom_syndrome|not_specified|not_provided|Monogenic_diabetes|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Monogenic_diabetes|Alstrom_syndrome|Retinal_dystrophy": 1,
    "not_specified|Alstrom_syndrome|Cardiovascular_phenotype|Retinal_dystrophy": 1,
    "not_provided|Cardiovascular_phenotype|ALMS1-related_disorder|not_specified|Alstrom_syndrome": 1,
    "Monogenic_diabetes|Alstrom_syndrome|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Alstrom_syndrome|not_specified": 1,
    "Hearing_impairment|not_specified|Cardiovascular_phenotype|Alstrom_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Retinal_dystrophy|Alstrom_syndrome": 1,
    "Cardiovascular_phenotype|Retinal_dystrophy|not_specified|not_provided|Alstrom_syndrome": 1,
    "Alstrom_syndrome|Cardiovascular_phenotype|not_specified|Monogenic_diabetes": 1,
    "Monogenic_diabetes|not_specified|Alstrom_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Alstrom_syndrome|Monogenic_diabetes": 1,
    "Cardiovascular_phenotype|Monogenic_diabetes|Alstrom_syndrome": 1,
    "Galloway-Mowat_syndrome_5|not_provided": 2,
    "TPRKB-related_disorder": 4,
    "Galloway-Mowat_syndrome_5": 4,
    "Galloway-Mowat_syndrome_5|not_specified": 1,
    "Nephrotic_syndrome|Galloway-Mowat_syndrome_5": 1,
    "TPRKB-related_disorder|not_provided": 1,
    "TPRKB-related_disorder|not_provided|not_specified": 1,
    "Microcephaly-capillary_malformation_syndrome": 15,
    "not_specified|not_provided|Microcephaly-capillary_malformation_syndrome": 1,
    "not_provided|STAMBP-related_disorder|Microcephaly-capillary_malformation_syndrome": 1,
    "not_provided|STAMBP-related_disorder": 4,
    "not_provided|Microcephaly-capillary_malformation_syndrome": 9,
    "STAMBP-related_disorder|not_provided": 1,
    "Microcephaly-capillary_malformation_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Microcephaly-capillary_malformation_syndrome": 1,
    "Microcephaly-capillary_malformation_syndrome|not_provided": 2,
    "not_specified|Microcephaly-capillary_malformation_syndrome|not_provided": 1,
    "not_provided|not_specified|Microcephaly-capillary_malformation_syndrome": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|not_provided|Visceral_myopathy_1": 1,
    "Visceral_myopathy_1|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|not_provided": 2,
    "Visceral_myopathy_1": 25,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5": 10,
    "Chronic_intestinal_pseudoobstruction": 3,
    "ACTG2-related_disorder|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|Visceral_myopathy_1|not_provided": 2,
    "Chronic_intestinal_pseudoobstruction|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|Visceral_myopathy_1|Visceral_neuropathy|_familial|_3|_autosomal_dominant|not_provided|Constipation": 1,
    "Visceral_myopathy_1|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5": 2,
    "ACTG2-related_disorder": 4,
    "ACTG2-related_disorder|not_provided": 1,
    "Visceral_myopathy_1|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|Visceral_myopathy_1": 1,
    "Megacystis|_microcolon|_hypoperistalsis_syndrome": 1,
    "Chronic_intestinal_pseudoobstruction|Visceral_myopathy_1": 1,
    "Visceral_myopathy_1|Intestinal_obstruction": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|not_provided|Inborn_genetic_diseases|Visceral_myopathy_1": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|not_provided|Visceral_myopathy_1|Inborn_genetic_diseases": 1,
    "Visceral_myopathy_1|not_provided|ACTG2-related_disorder": 1,
    "Visceral_myopathy_1|not_provided": 1,
    "Visceral_myopathy_1|ACTG2-related_disorder": 1,
    "ACTG2-related_disorder|Visceral_myopathy_1|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|Visceral_myopathy_1|Inborn_genetic_diseases|Megacystis|Chronic_intestinal_pseudoobstruction|Visceral_neuropathy|_familial|_3|_autosomal_dominant|not_provided": 1,
    "Visceral_myopathy_1|Inborn_genetic_diseases|Chronic_intestinal_pseudoobstruction|Megacystis|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_5|not_provided": 1,
    "Intestinal_pseudo-obstruction": 1,
    "Mitochondrial_DNA_depletion_syndrome|not_provided|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 18,
    "DGUOK-related_disorder": 8,
    "DGUOK-related_disorder|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|not_provided": 5,
    "DGUOK-related_disorder|not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 2,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Portal_hypertension|_noncirrhotic|_1": 2,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Inborn_genetic_diseases": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4": 4,
    "not_provided|DGUOK-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|DGUOK-related_disorder": 7,
    "DGUOK-related_disorder|not_provided": 9,
    "not_provided|Increased_circulating_pyruvate_concentration|Migraine_with_aura|Increased_CSF_lactate|Cognitive_impairment|Hypoplasia_of_the_corpus_callosum|Cerebral_atrophy|Memory_impairment|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_disease": 4,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 3,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|not_provided": 1,
    "Portal_hypertension|_noncirrhotic|_1|not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Portal_hypertension|_noncirrhotic": 1,
    "not_specified|not_provided|DGUOK-related_disorder": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 7,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Portal_hypertension|_noncirrhotic|_1": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Portal_hypertension|_noncirrhotic|_1|not_specified|DGUOK-related_disorder": 1,
    "not_provided|Portal_hypertension|_noncirrhotic|_1|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4": 1,
    "Increased_circulating_pyruvate_concentration|Migraine_with_aura|Increased_CSF_lactate|Cognitive_impairment|Hypoplasia_of_the_corpus_callosum|Cerebral_atrophy|Memory_impairment|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|DGUOK-related_disorder": 1,
    "DGUOK-related_disorder|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|not_provided|not_specified": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4": 1,
    "not_specified|DGUOK-related_disorder": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Portal_hypertension|_noncirrhotic|_1": 1,
    "not_specified|DGUOK-related_disorder|not_provided": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Portal_hypertension|_noncirrhotic|_1|Inborn_genetic_diseases|DGUOK-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|DGUOK-related_disorder|not_provided": 2,
    "Portal_hypertension|_noncirrhotic|_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|not_provided|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|not_provided|Portal_hypertension|_noncirrhotic|_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|DGUOK-related_disorder|Portal_hypertension|_noncirrhotic": 1,
    "DGUOK-related_disorder|not_provided|Mitochondrial_DNA_depletion_syndrome": 1,
    "Portal_hypertension|_noncirrhotic|_1|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|not_provided": 1,
    "not_provided|DGUOK-related_disorder|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Portal_hypertension|_noncirrhotic|_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|DGUOK-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "not_provided|See_cases|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)": 1,
    "Portal_hypertension": 1,
    "DGUOK-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DGUOK-related_disorder|Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Portal_hypertension|_noncirrhotic|_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|Portal_hypertension|_noncirrhotic|_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4": 1,
    "Mitochondrial_DNA_depletion_syndrome_3_(hepatocerebral_type)|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_4|Portal_hypertension|_noncirrhotic|not_specified": 1,
    "Beck-Fahrner_syndrome": 72,
    "TET3-related_disorder": 38,
    "Beck-Fahrner_syndrome|not_provided": 5,
    "not_provided|Beck-Fahrner_syndrome": 8,
    "not_provided|TET3-related_disorder": 10,
    "TET3-related_disorder|not_provided": 6,
    "Inborn_genetic_diseases|Beck-Fahrner_syndrome|not_provided": 1,
    "Beck-Fahrner_syndrome|TET3_deficiency": 6,
    "not_provided|Inborn_genetic_diseases|Beck-Fahrner_syndrome": 1,
    "TET3-related_disorder|not_specified|not_provided": 1,
    "Beck-Fahrner_syndrome|Inborn_genetic_diseases|TET3_deficiency|not_provided": 1,
    "TET3-related_disorder|not_provided|Beck-Fahrner_syndrome": 1,
    "Beck-Fahrner_syndrome|Inborn_genetic_diseases|TET3_deficiency": 1,
    "Beck-Fahrner_syndrome|Intellectual_disability|TET3_deficiency": 1,
    "Beck-Fahrner_syndrome|TET3-related_disorder": 2,
    "Inborn_genetic_diseases|Beck-Fahrner_syndrome": 3,
    "Beck-Fahrner_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Beck-Fahrner_syndrome|TET3_deficiency": 1,
    "Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities": 40,
    "Multiple_mitochondrial_dysfunctions_syndrome_2": 19,
    "not_provided|BOLA3-related_disorder|Multiple_mitochondrial_dysfunctions_syndrome_2": 1,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_2|Inborn_genetic_diseases": 2,
    "Multiple_mitochondrial_dysfunctions_syndrome_2|not_specified|not_provided": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_2|not_provided": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_2|not_provided|BOLA3-related_disorder": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_2|BOLA3-related_disorder|not_provided": 1,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_2": 3,
    "BOLA3-related_disorder|Multiple_mitochondrial_dysfunctions_syndrome_2|not_specified|not_provided": 1,
    "SLC4A5-related_disorder": 13,
    "SLC4A5-related_disorder|not_provided": 1,
    "not_provided|SLC4A5-related_disorder": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 8,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 9,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 457,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 57,
    "Inborn_genetic_diseases|not_specified|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 214,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1": 34,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases": 22,
    "not_provided|DCTN1-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|DCTN1-related_disorder|Inborn_genetic_diseases": 3,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|not_provided": 3,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis|not_provided": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 69,
    "DCTN1-related_disorder|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 3,
    "Perry_syndrome|DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Inborn_genetic_diseases|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 6,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1": 1,
    "DCTN1-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 6,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 54,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis|_susceptibility_to": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Inborn_genetic_diseases": 2,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|not_provided": 4,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Peripheral_neuropathy": 1,
    "not_provided|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 1,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 12,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_specified|not_provided": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|DCTN1-related_disorder|not_provided": 1,
    "DCTN1-related_disorder": 14,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 2,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1": 2,
    "Inborn_genetic_diseases|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 5,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 2,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_provided": 12,
    "Neuronopathy|_distal_hereditary_motor|_type_7B": 4,
    "DCTN1-related_disorder|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_7B|Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided": 6,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 16,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 4,
    "not_specified|DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases": 8,
    "DCTN1-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|not_provided": 2,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided|DCTN1-related_disorder": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_provided": 4,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 16,
    "not_specified|Inborn_genetic_diseases|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Amyotrophic_lateral_sclerosis|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 21,
    "Perry_syndrome": 12,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|DCTN1-related_disorder": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases": 2,
    "DCTN1-related_disorder|not_specified|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|DCTN1-related_disorder": 8,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 16,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided|not_specified": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided|Inborn_genetic_diseases|not_specified|DCTN1-related_disorder": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided": 3,
    "not_provided|DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases|DCTN1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 2,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided|Inborn_genetic_diseases": 2,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided|DCTN1-related_disorder|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Inborn_genetic_diseases|DCTN1-related_disorder|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis|DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided": 9,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder": 5,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_specified": 1,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 7,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|not_provided|DCTN1-related_disorder": 1,
    "DCTN1-related_disorder|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|DCTN1-related_disorder|not_provided": 2,
    "not_provided|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder": 2,
    "not_specified|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 2,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_specified|Inborn_genetic_diseases": 1,
    "DCTN1-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1": 3,
    "Amyotrophic_lateral_sclerosis_type_1": 164,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder": 3,
    "not_provided|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases|not_provided": 1,
    "DCTN1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided|Amyotrophic_lateral_sclerosis|_susceptibility_to": 1,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|DCTN1-related_disorder": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_specified|DCTN1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Amyotrophic_lateral_sclerosis|DCTN1-related_disorder|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Perry_syndrome|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Hereditary_motor_neuron_disease|Inborn_genetic_diseases": 1,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_disease|Perry_syndrome": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder|Inborn_genetic_diseases|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "not_provided|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 3,
    "Inborn_genetic_diseases|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "DCTN1-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided|DCTN1-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified": 2,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis|_susceptibility_to": 1,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Perry_syndrome|not_provided|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Inborn_genetic_diseases|DCTN1-related_disorder|not_provided": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Inborn_genetic_diseases|DCTN1-related_disorder": 1,
    "not_provided|Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified": 1,
    "Inborn_genetic_diseases|DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 3,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1": 2,
    "DCTN1-related_disorder|not_specified|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Perry_syndrome|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|not_provided": 3,
    "DCTN1-related_disorder|not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Frontotemporal_dementia": 1,
    "DCTN1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Inborn_genetic_diseases": 2,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|DCTN1-related_disorder|Inborn_genetic_diseases": 1,
    "Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 1,
    "DCTN1-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified": 1,
    "Amyotrophic_lateral_sclerosis|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|DCTN1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|not_specified|Parkinsonian_disorder|DCTN1-related_disorder": 1,
    "DCTN1-related_disorder|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 2,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Distal_spinal_muscular_atrophy": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|DCTN1-related_disorder": 2,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_provided|Amyotrophic_lateral_sclerosis|not_specified": 1,
    "Generalized_dystonia|Dystonic_disorder|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Inborn_genetic_diseases|DCTN1-related_disorder|not_specified": 1,
    "not_specified|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|See_cases|not_provided|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|DCTN1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|not_specified|DCTN1-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|not_specified|DCTN1-related_disorder": 1,
    "not_provided|Hereditary_motor_neuron_disease|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "Amyotrophic_lateral_sclerosis|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "not_provided|Perry_syndrome": 2,
    "Hereditary_motor_neuron_disease|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B": 1,
    "not_provided|DCTN1-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "DCTN1-related_disorder|Amyotrophic_lateral_sclerosis": 1,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|Perry_syndrome": 1,
    "Inborn_genetic_diseases|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|not_provided|DCTN1-related_disorder": 1,
    "DCTN1-related_disorder|not_provided|Inborn_genetic_diseases|Perry_syndrome|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1": 1,
    "not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_type_7B|Amyotrophic_lateral_sclerosis_type_1|Perry_syndrome": 1,
    "Perry_syndrome|Amyotrophic_lateral_sclerosis_type_1|Neuronopathy|_distal_hereditary_motor|_type_7B|DCTN1-related_disorder": 1,
    "Perry_syndrome|Distal_spinal_muscular_atrophy": 1,
    "MOGS-congenital_disorder_of_glycosylation": 410,
    "MOGS-congenital_disorder_of_glycosylation|not_provided": 6,
    "MOGS-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided": 1,
    "MOGS-related_disorder": 3,
    "Inborn_genetic_diseases|MOGS-congenital_disorder_of_glycosylation": 20,
    "MOGS-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 33,
    "MOGS-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "MOGS-related_disorder|MOGS-congenital_disorder_of_glycosylation": 4,
    "MOGS-congenital_disorder_of_glycosylation|not_specified": 3,
    "MOGS-congenital_disorder_of_glycosylation|MOGS-related_disorder": 6,
    "not_provided|MOGS-congenital_disorder_of_glycosylation": 6,
    "MOGS-congenital_disorder_of_glycosylation|not_provided|not_specified": 4,
    "not_specified|not_provided|MOGS-congenital_disorder_of_glycosylation": 5,
    "MOGS-related_disorder|not_specified|MOGS-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|MOGS-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|MOGS-related_disorder|MOGS-congenital_disorder_of_glycosylation": 1,
    "not_provided|MOGS-congenital_disorder_of_glycosylation|not_specified": 3,
    "not_provided|MOGS-congenital_disorder_of_glycosylation|MOGS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|MOGS-congenital_disorder_of_glycosylation": 2,
    "MOGS-related_disorder|not_provided|MOGS-congenital_disorder_of_glycosylation": 1,
    "MOGS-congenital_disorder_of_glycosylation|MOGS-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|MOGS-congenital_disorder_of_glycosylation": 1,
    "not_specified|MOGS-congenital_disorder_of_glycosylation": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|MOGS-congenital_disorder_of_glycosylation": 1,
    "MOGS-congenital_disorder_of_glycosylation|not_specified|MOGS-related_disorder|not_provided": 1,
    "Parkinson_disease_13|_autosomal_dominant|_susceptibility_to": 24,
    "not_provided|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to": 10,
    "Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|not_provided": 6,
    "Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|not_specified": 1,
    "not_provided|HTRA2-related_disorder": 1,
    "3-methylglutaconic_aciduria_type_8|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "not_provided|3-methylglutaconic_aciduria_type_8": 3,
    "HTRA2-related_disorder|not_provided": 1,
    "not_provided|HTRA2-related_disorder|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to": 2,
    "not_provided|HTRA2-Related_Disorders": 1,
    "not_specified|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "3-methylglutaconic_aciduria_type_8|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to": 2,
    "Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|3-methylglutaconic_aciduria_type_8|not_provided": 1,
    "HTRA2-related_disorder|3-methylglutaconic_aciduria_type_8|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "3-methylglutaconic_aciduria_type_8|not_provided": 2,
    "not_provided|3-methylglutaconic_aciduria_type_8|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to": 1,
    "3-methylglutaconic_aciduria_type_8": 6,
    "HTRA2-related_disorder|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "HTRA2-related_disorder": 2,
    "not_provided|Parkinson_disease_13|_autosomal_dominant|_susceptibility_to|3-methylglutaconic_aciduria_type_8": 1,
    "not_provided|LOXL3-related_disorder": 8,
    "LOXL3-related_disorder": 6,
    "LOXL3-related_disorder|not_provided": 5,
    "LOXL3-related_disorder|Stickler_syndrome|not_provided": 1,
    "Myopia_28|_autosomal_recessive|not_provided": 2,
    "not_provided|Myopia_28|_autosomal_recessive|Stickler_syndrome_type_1": 1,
    "not_provided|Myopia_28|_autosomal_recessive": 1,
    "Myopia_28|_autosomal_recessive": 3,
    "not_specified|not_provided|Myopia_28|_autosomal_recessive": 1,
    "Spermatogenic_failure_48|Spermatogenesis_maturation_arrest": 1,
    "Spermatogenic_failure_48": 3,
    "Spermatogenic_failure_48|Non-obstructive_azoospermia": 1,
    "Non-obstructive_azoospermia|Spermatogenic_failure_48": 1,
    "Non-obstructive_azoospermia|Cryptozoospermia|Spermatogenic_failure_48": 1,
    "Non-obstructive_azoospermia|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Spermatogenic_failure_48|not_provided": 1,
    "not_specified|M1AP-related_condition": 1,
    "HK2-related_disorder": 24,
    "HK2-related_disorder|not_provided": 1,
    "TACR1-related_disorder": 3,
    "EVA1A-related_disorder": 4,
    "LRRTM4-related_disorder": 4,
    "not_provided|Cortical_dysplasia|_complex|_with_other_brain_malformations_9": 1,
    "CTNNA2-related_disorder": 14,
    "not_provided|CTNNA2-related_disorder": 3,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_9": 8,
    "Inborn_genetic_diseases|CTNNA2-related_disorder": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia|_complex|_with_other_brain_malformations_9": 1,
    "CTNNA2-related_disorder|not_provided": 3,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_9|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_9|not_provided": 1,
    "CTNNA2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_9": 7,
    "Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_DNA_depletion_syndrome_9": 3,
    "Mitochondrial_DNA_depletion_syndrome_9": 192,
    "Mitochondrial_DNA_depletion_syndrome_9|Mitochondrial_DNA_depletion_syndrome|not_provided": 2,
    "Mitochondrial_DNA_depletion_syndrome_9|Mitochondrial_DNA_depletion_syndrome": 5,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_9": 22,
    "Mitochondrial_DNA_depletion_syndrome_9|not_provided|Mitochondrial_DNA_depletion_syndrome": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|not_provided": 8,
    "Mitochondrial_DNA_depletion_syndrome|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_9": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|Inborn_genetic_diseases": 5,
    "Mitochondrial_DNA_depletion_syndrome_9|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_9": 4,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_9": 6,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_9|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|SUCLG1-related_disorder|Mitochondrial_DNA_depletion_syndrome|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|not_specified|not_provided": 1,
    "SUCLG1-related_disorder|not_specified": 1,
    "SUCLG1-related_disorder|Mitochondrial_DNA_depletion_syndrome_9": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_9|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_DNA_depletion_syndrome_9|SUCLG1-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_9|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|not_specified": 3,
    "SUCLG1-related_disorder|Mitochondrial_DNA_depletion_syndrome|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_9": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|SUCLG1-related_disorder|Mitochondrial_DNA_depletion_syndrome|not_provided|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|Mitochondrial_DNA_depletion_syndrome|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_9|not_provided": 3,
    "not_provided|SUCLG1-related_disorder|Mitochondrial_DNA_depletion_syndrome_9": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_9": 1,
    "Mitochondrial_DNA_depletion_syndrome_9|not_provided|SUCLG1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_DNA_depletion_syndrome_9": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_9|not_specified|not_provided": 1,
    "SUCLG1-related_disorder|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_9|not_specified": 1,
    "DNAH6-related_disorder|not_provided": 5,
    "DNAH6-related_disorder": 41,
    "DNAH6-related_disorder|not_specified|not_provided": 5,
    "DNAH6-related_disorder|not_specified": 2,
    "DNAH6-related_disorder|not_provided|not_specified": 3,
    "Heterotaxy": 9,
    "not_provided|DNAH6-related_disorder": 7,
    "Abnormal_spermatogenesis": 2,
    "Spermatogenic_Failure|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_45": 5,
    "not_specified|DNAH6-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_88|Hearing_loss|_autosomal_dominant_81": 1,
    "ELMOD3-related_disorder|not_provided|not_specified": 2,
    "ELMOD3-related_disorder": 2,
    "ELMOD3-related_disorder|not_provided": 2,
    "Hearing_loss|_autosomal_dominant_81|Autosomal_recessive_nonsyndromic_hearing_loss_88|not_provided": 2,
    "not_specified|ELMOD3-related_disorder|not_provided": 1,
    "not_specified|ELMOD3-related_disorder": 1,
    "not_provided|ELMOD3-related_disorder": 5,
    "Hearing_loss|_autosomal_dominant_81": 3,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_88|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_88": 1,
    "not_specified|not_provided|ELMOD3-related_disorder": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 24,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 16,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|MAT2A-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 2,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "not_specified|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MAT2A-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "MAT2A-related_disorder": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "MAT2A-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "MAT2A-related_disorder|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Vitamin_K-Dependent_Clotting_Factors": 17,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1": 128,
    "not_provided|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1": 39,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|not_provided": 13,
    "not_provided|Vitamin_K-Dependent_Clotting_Factors": 4,
    "GGCX-related_disorder": 4,
    "not_provided|GGCX-related_disorder": 7,
    "not_provided|Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency": 3,
    "Inborn_genetic_diseases|not_provided|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1": 2,
    "not_provided|GGCX_-_Related_Disorders": 1,
    "not_provided|Abnormal_bleeding|Thrombocytopenia": 4,
    "GGCX-related_disorder|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency|not_provided": 1,
    "not_provided|Acute_myeloid_leukemia": 11,
    "GGCX-related_disorder|not_provided|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1": 4,
    "GGCX-related_disorder|not_provided": 4,
    "Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency": 8,
    "GGCX-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|Thrombocytopenia|Abnormal_bleeding": 1,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|GGCX-related_disorder": 1,
    "Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency|not_provided|GGCX_-_Related_Disorders|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1": 1,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|Inborn_genetic_diseases": 2,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|Body_skin_hyperlaxity_due_to_vitamin_K-dependent_coagulation_factor_deficiency": 1,
    "Inborn_genetic_diseases|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1|not_provided": 1,
    "not_provided|GGCX-related_disorder|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_1": 1,
    "Vitamin_K-Dependent_Clotting_Factors|not_provided": 2,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1": 38,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1": 7,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_provided": 6,
    "Hereditary_pulmonary_alveolar_proteinosis": 357,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|Hereditary_pulmonary_alveolar_proteinosis": 7,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided": 85,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_1|not_provided": 2,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis": 68,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_1": 3,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_specified|not_provided|Hereditary_pulmonary_alveolar_proteinosis": 2,
    "SFTPB-related_disorder|not_provided|Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_1": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|Hereditary_pulmonary_alveolar_proteinosis|not_specified|not_provided": 1,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1|Hereditary_pulmonary_alveolar_proteinosis": 4,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1": 2,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_provided|Hereditary_pulmonary_alveolar_proteinosis": 4,
    "not_provided|SFTPB-related_disorder": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|SFTPB-related_disorder|not_provided": 1,
    "SFTPB-related_disorder": 2,
    "SFTPB-related_disorder|not_provided|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_specified": 1,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1|SFTPB-related_disorder": 1,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1|not_specified|Hereditary_pulmonary_alveolar_proteinosis": 2,
    "SFTPB-related_disorder|not_specified|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1": 1,
    "SFTPB-related_disorder|Surfactant_metabolism_dysfunction|_pulmonary|_1|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_provided|not_specified|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "SFTPB-related_disorder|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_1": 1,
    "not_specified|Hereditary_pulmonary_alveolar_proteinosis": 2,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_specified|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 1,
    "SFTPB-related_disorder|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_1|not_provided|Hereditary_pulmonary_alveolar_proteinosis|not_specified": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_1": 1,
    "GM3_synthase_deficiency": 388,
    "GM3_synthase_deficiency|not_provided": 15,
    "Intellectual_disability|GM3_synthase_deficiency": 2,
    "GM3_synthase_deficiency|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|not_provided|GM3_synthase_deficiency": 3,
    "not_provided|GM3_synthase_deficiency": 12,
    "GM3_synthase_deficiency|Inborn_genetic_diseases": 5,
    "not_provided|GM3_synthase_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|GM3_synthase_deficiency": 2,
    "Inborn_genetic_diseases|GM3_synthase_deficiency": 9,
    "Inborn_genetic_diseases|not_provided|GM3_synthase_deficiency": 2,
    "ST3GAL5-related_disorder|GM3_synthase_deficiency|not_provided": 2,
    "ST3GAL5-related_disorder|not_provided|GM3_synthase_deficiency": 1,
    "not_provided|GM3_synthase_deficiency|not_specified": 1,
    "GM3_synthase_deficiency|ST3GAL5-related_disorder": 1,
    "not_provided|POLR1A-related_disorder": 10,
    "Inborn_genetic_diseases|Acrofacial_dysostosis_Cincinnati_type|Leukodystrophy|_hypomyelinating|_27": 1,
    "not_provided|Acrofacial_dysostosis_Cincinnati_type": 4,
    "Acrofacial_dysostosis_Cincinnati_type": 16,
    "not_specified|not_provided|Leukodystrophy|_hypomyelinating|_27|Acrofacial_dysostosis_Cincinnati_type|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Acrofacial_dysostosis_Cincinnati_type": 1,
    "not_provided|See_cases|POLR1A-related_disorder": 1,
    "Inborn_genetic_diseases|Leukodystrophy|_hypomyelinating|_27|not_provided": 1,
    "Acrofacial_dysostosis_Cincinnati_type|not_provided": 9,
    "POLR1A-related_disorder|not_provided": 6,
    "POLR1A-related_disorder": 2,
    "Leukodystrophy|_hypomyelinating|_27": 1,
    "Acrofacial_dysostosis_Cincinnati_type|Inborn_genetic_diseases": 1,
    "Multiple_congenital_anomalies/dysmorphic_syndrome": 10,
    "POLR1A-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Acrofacial_dysostosis_Cincinnati_type|Inborn_genetic_diseases": 1,
    "Leukodystrophy|_hypomyelinating|_27|Acrofacial_dysostosis_Cincinnati_type": 1,
    "Acrofacial_dysostosis_Cincinnati_type|Leukodystrophy|_hypomyelinating|_27|not_provided": 1,
    "POLR1A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Acrofacial_dysostosis_Cincinnati_type|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Leukodystrophy|_hypomyelinating|_27|Acrofacial_dysostosis_Cincinnati_type": 1,
    "not_provided|Leukodystrophy|_hypomyelinating|_27|Acrofacial_dysostosis_Cincinnati_type": 1,
    "Intellectual_disability|_autosomal_dominant_9": 40,
    "PTCD3-related_disorder": 5,
    "Combined_oxidative_phosphorylation_deficiency_51": 9,
    "See_cases|Combined_oxidative_phosphorylation_deficiency_51": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency_51": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_51": 1,
    "not_provided|Hereditary_spastic_paraplegia_31": 26,
    "Hereditary_spastic_paraplegia_31": 219,
    "Hereditary_spastic_paraplegia_31|not_provided": 11,
    "Spastic_paraplegia|_autosomal_dominant|not_provided": 4,
    "Hereditary_spastic_paraplegia_31|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spinal_muscular_atrophy|_distal|_autosomal_recessive|_6|Hereditary_spastic_paraplegia_31|Neuronopathy|_distal_hereditary_motor|_type_5B|not_provided|REEP1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_31": 1,
    "REEP1-related_disorder|not_provided": 1,
    "REEP1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5B|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_31": 1,
    "REEP1-related_disorder|Hereditary_spastic_paraplegia_31": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_spastic_paraplegia_31|Spasticity|REEP1-related_disorder|not_provided": 1,
    "Polyneuropathy|not_provided": 1,
    "Hereditary_spastic_paraplegia_31|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_31|not_specified": 4,
    "not_provided|Hereditary_spastic_paraplegia_31|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5B": 4,
    "Hereditary_spastic_paraplegia_31|Neuronopathy|_distal_hereditary_motor|_type_5B": 1,
    "Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases": 9,
    "Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_31": 7,
    "Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_5B": 1,
    "Hereditary_spastic_paraplegia_31|REEP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases|REEP1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_31|REEP1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_31": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5B|Spinal_muscular_atrophy|_distal|_autosomal_recessive|_6|Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_31": 1,
    "Hereditary_spastic_paraplegia_31|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_31|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_31|REEP1-related_disorder": 2,
    "not_specified|Hereditary_spastic_paraplegia_31": 2,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_5B|Hereditary_spastic_paraplegia_31": 3,
    "Hereditary_spastic_paraplegia_31|Hereditary_spastic_paraplegia": 3,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_31": 1,
    "not_specified|Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_31|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia_31|Hereditary_spastic_paraplegia": 1,
    "Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_5B": 1,
    "Spinal_muscular_atrophy|_distal|_autosomal_recessive|_6": 1,
    "REEP1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_31|Neuronopathy|_distal_hereditary_motor|_type_5B|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "Spinal_muscular_atrophy|_distal|_autosomal_recessive|_6|Neuronopathy|_distal_hereditary_motor|_type_5B": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_31": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5B|Hereditary_spastic_paraplegia_31": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_31|not_specified": 1,
    "Hereditary_spastic_paraplegia_31|Spinal_muscular_atrophy|_distal|_autosomal_recessive|_6": 1,
    "Hereditary_spastic_paraplegia_31|Charcot-Marie-Tooth_disease": 1,
    "Hereditary_spastic_paraplegia_31|Neuronopathy|_distal_hereditary_motor|_type_5B|Spinal_muscular_atrophy|_distal|_autosomal_recessive|_6": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_31": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_31|Hereditary_spastic_paraplegia": 1,
    "REEP1-related_disorder|Hereditary_spastic_paraplegia_31|not_provided": 1,
    "REEP1-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_31": 1,
    "Hereditary_spastic_paraplegia_31|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|REEP1-related_disorder": 1,
    "KDM3A-related_disorder|not_provided": 2,
    "KDM3A-related_disorder": 21,
    "not_provided|KDM3A-related_disorder": 1,
    "Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation": 162,
    "Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation|CD8A-related_disorder": 2,
    "not_specified|Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation": 2,
    "Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation|not_specified": 2,
    "CD8A-related_disorder|Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation": 1,
    "Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation|not_specified|not_provided": 2,
    "Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation|not_provided": 3,
    "not_provided|Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation": 5,
    "not_provided|Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation|CD8A-related_disorder": 1,
    "CD8A-related_disorder": 1,
    "not_specified|not_provided|Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation": 1,
    "not_provided|CD8A-related_disorder|Susceptibility_to_respiratory_infections_associated_with_CD8alpha_chain_mutation": 1,
    "not_provided|Craniofacial_microsomia_1": 3,
    "Craniofacial_microsomia_2": 2,
    "Craniofacial_microsomia_1|not_provided": 1,
    "Craniofacial_microsomia_1|not_provided|Craniofacial_microsomia|Craniofacial_microsomia_2": 1,
    "Craniofacial_microsomia_1|not_provided|Craniofacial_microsomia_2": 1,
    "Craniofacial_microsomia|Craniofacial_microsomia_2": 2,
    "Craniofacial_microsomia": 9,
    "FOXI3-related_disorder|not_provided": 2,
    "not_provided|FOXI3-related_disorder": 1,
    "not_provided|Wolcott-Rallison_dysplasia": 40,
    "Wolcott-Rallison_dysplasia": 137,
    "Wolcott-Rallison_dysplasia|Inborn_genetic_diseases|not_provided": 3,
    "Wolcott-Rallison_dysplasia|Connective_tissue_disorder|not_specified|not_provided": 1,
    "Wolcott-Rallison_dysplasia|not_provided": 37,
    "not_provided|Inborn_genetic_diseases|Wolcott-Rallison_dysplasia": 2,
    "Wolcott-Rallison_dysplasia|not_specified": 1,
    "Wolcott-Rallison_dysplasia|Inborn_genetic_diseases": 5,
    "EIF2AK3-related_disorder": 2,
    "not_specified|Connective_tissue_disorder|Wolcott-Rallison_dysplasia|not_provided": 1,
    "not_specified|Wolcott-Rallison_dysplasia": 1,
    "Inborn_genetic_diseases|not_provided|Wolcott-Rallison_dysplasia": 3,
    "not_provided|Wolcott-Rallison_dysplasia|Inborn_genetic_diseases": 2,
    "not_provided|EIF2AK3-related_disorder|Wolcott-Rallison_dysplasia": 1,
    "Inborn_genetic_diseases|Wolcott-Rallison_dysplasia|not_provided": 5,
    "not_specified|Wolcott-Rallison_dysplasia|not_provided": 2,
    "not_specified|Wolcott-Rallison_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "Menkes_kinky-hair_syndrome|not_provided": 7,
    "EIF2AK3-related_disorder|Wolcott-Rallison_dysplasia|not_provided": 1,
    "EIF2AK3-related_disorder|not_provided": 3,
    "not_provided|not_specified|Wolcott-Rallison_dysplasia": 1,
    "Monogenic_diabetes|not_specified|not_provided|Wolcott-Rallison_dysplasia": 1,
    "Connective_tissue_disorder|not_provided|Wolcott-Rallison_dysplasia|Monogenic_diabetes": 1,
    "Wolcott-Rallison_dysplasia|EIF2AK3-related_disorder|not_provided": 2,
    "EIF2AK3-related_disorder|not_provided|Connective_tissue_disorder|Monogenic_diabetes|not_specified|Wolcott-Rallison_dysplasia": 1,
    "not_provided|EIF2AK3-related_disorder": 2,
    "not_provided|Wolcott-Rallison_dysplasia|EIF2AK3-related_disorder|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|Wolcott-Rallison_dysplasia": 1,
    "Wolcott-Rallison_dysplasia|Connective_tissue_disorder|not_provided": 1,
    "Wolcott-Rallison_dysplasia|not_provided|EIF2AK3-related_disorder": 1,
    "Wolcott-Rallison_dysplasia|not_provided|Inborn_genetic_diseases": 3,
    "EIF2AK3-related_disorder|Monogenic_diabetes|not_provided|not_specified|Wolcott-Rallison_dysplasia": 1,
    "Wolcott-Rallison_dysplasia|EIF2AK3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Wolcott-Rallison_dysplasia|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "Wolcott-Rallison_dysplasia|not_provided|not_specified|Connective_tissue_disorder": 1,
    "Wolcott-Rallison_dysplasia|not_specified|not_provided": 2,
    "Monogenic_diabetes|Wolcott-Rallison_dysplasia|not_provided": 1,
    "EIF2AK3-related_disorder|Connective_tissue_disorder|Monogenic_diabetes|not_specified|not_provided|Wolcott-Rallison_dysplasia": 1,
    "Monogenic_diabetes|not_provided|Wolcott-Rallison_dysplasia|Inborn_genetic_diseases": 1,
    "EIF2AK3-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Connective_tissue_disorder|Wolcott-Rallison_dysplasia|not_provided": 1,
    "not_specified|not_provided|Wolcott-Rallison_dysplasia": 1,
    "Inborn_genetic_diseases|not_provided|Wolcott-Rallison_dysplasia|EIF2AK3-related_disorder": 1,
    "Deficiency_of_ribose-5-phosphate_isomerase": 27,
    "Deficiency_of_ribose-5-phosphate_isomerase|not_provided": 5,
    "RPIA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Deficiency_of_ribose-5-phosphate_isomerase": 3,
    "RPIA-related_disorder": 1,
    "not_provided|Deficiency_of_ribose-5-phosphate_isomerase": 4,
    "Deficiency_of_ribose-5-phosphate_isomerase|Inborn_genetic_diseases": 1,
    "RPIA-related_disorder|not_provided|Deficiency_of_ribose-5-phosphate_isomerase": 1,
    "RPIA-related_disorder|not_provided": 1,
    "Recurrent_infections_associated_with_rare_immunoglobulin_isotypes_deficiency": 2,
    "not_provided|Peritoneal_Gliomatosis": 2,
    "ADRA2B-related_disorder": 9,
    "Epilepsy|_familial_adult_myoclonic|_2": 4,
    "not_provided|Epilepsy|_familial_adult_myoclonic|_2|not_specified": 1,
    "not_specified|Epilepsy|_familial_adult_myoclonic|_2": 3,
    "Oocyte_maturation_defect_11": 1,
    "Epilepsy|_familial_adult_myoclonic|_2|not_specified": 2,
    "STARD7-related_disorder": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 7,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 23,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 9,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided": 25,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|TMEM127-related_disorder|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 8,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma": 3,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|TMEM127-related_disorder|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 3,
    "Hereditary_cancer-predisposing_syndrome|Uveal_melanoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided|TMEM127-related_disorder|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 2,
    "not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_pheochromocytoma-paraganglioma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 14,
    "Pheochromocytoma|_susceptibility_to|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 3,
    "Hereditary_pheochromocytoma-paraganglioma|TMEM127-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 9,
    "Pheochromocytoma|_susceptibility_to|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|TMEM127-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|_susceptibility_to|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_provided": 2,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided": 5,
    "TMEM127-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 1,
    "Pheochromocytoma|_susceptibility_to|not_provided|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma": 2,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|TMEM127-related_disorder": 1,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|TMEM127-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|_susceptibility_to|Pheochromocytoma": 1,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided|Hereditary_pheochromocytoma-paraganglioma|TMEM127-related_disorder": 1,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "TMEM127-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Acute_myeloid_leukemia|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|TMEM127-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 1,
    "Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Hereditary_pheochromocytoma-paraganglioma|not_specified|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_10": 1,
    "Acute_promyelocytic_leukemia|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "TMEM127-related_disorder": 1,
    "Neuromuscular_disease|Multiple_mitochondrial_dysfunctions_syndrome_10": 2,
    "Multiple_mitochondrial_dysfunctions_syndrome_10": 2,
    "Autosomal_dominant_retinitis_pigmentosa|not_provided": 2,
    "not_provided|SNRNP200-related_disorder|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_33|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|SNRNP200-related_disorder|not_provided|Retinal_dystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa_33": 1,
    "Retinitis_pigmentosa_33": 14,
    "SNRNP200-related_disorder|not_provided": 16,
    "Retinitis_pigmentosa_33|Retinitis_pigmentosa|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_33": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_33": 1,
    "Rod-cone_dystrophy": 16,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_33|not_provided": 2,
    "Retinitis_pigmentosa|SNRNP200-related_disorder|not_provided": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_33": 2,
    "SNRNP200-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 8,
    "not_provided|Retinitis_pigmentosa_33|SNRNP200-related_disorder": 2,
    "not_provided|SNRNP200-related_disorder": 7,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_33": 1,
    "Retinal_dystrophy|not_provided|SNRNP200-related_disorder": 1,
    "Retinitis_pigmentosa_33|Retinal_dystrophy|not_provided": 2,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_33": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_33": 1,
    "not_provided|Retinitis_pigmentosa_33|Retinal_dystrophy": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_33": 1,
    "Rod-cone_dystrophy|SNRNP200-related_disorder|not_provided": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa_33|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_33": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_33": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_33": 1,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided": 6,
    "Retinal_dystrophy|not_provided|Autosomal_dominant_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_33|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_33|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_33": 1,
    "Retinitis_pigmentosa_33|not_provided": 1,
    "not_provided|SNRNP200-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "SNRNP200-related_disorder|Retinitis_pigmentosa_33|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_33|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_33": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_33": 1,
    "Retinitis_pigmentosa|not_provided|SNRNP200-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa|SNRNP200-related_disorder": 1,
    "NCAPH-related_disorder": 9,
    "Microcephaly_23|_primary|_autosomal_recessive": 4,
    "not_provided|NCAPH-related_disorder|Microcephaly_23|_primary|_autosomal_recessive": 2,
    "ARID5A-related_disorder": 6,
    "ARID5A-related_disorder|not_specified": 1,
    "LMAN2L-related_disorder": 5,
    "Intellectual_developmental_disorder|_autosomal_dominant_69": 1,
    "Intellectual_disability|_autosomal_recessive_52": 8,
    "not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_4": 1,
    "Intellectual_disability|_autosomal_recessive_52|not_provided": 1,
    "Jalili_syndrome": 65,
    "not_provided|Jalili_syndrome": 9,
    "CNNM4-related_disorder|Jalili_syndrome|Inborn_genetic_diseases|not_provided|Retinal_dystrophy": 1,
    "not_provided|CNNM4-related_disorder": 2,
    "not_specified|not_provided|Jalili_syndrome": 1,
    "Jalili_syndrome|not_provided": 9,
    "CNNM4-related_disorder|not_provided|Jalili_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Jalili_syndrome": 5,
    "not_provided|CNNM4-related_disorder|Jalili_syndrome": 1,
    "Jalili_syndrome|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Jalili_syndrome|Inborn_genetic_diseases": 2,
    "CNNM4-related_disorder": 2,
    "Jalili_syndrome|Retinal_dystrophy": 1,
    "CNNM4-related_disorder|Jalili_syndrome|not_provided": 2,
    "not_provided|not_specified|Jalili_syndrome": 1,
    "CNNM4-related_disorder|Inborn_genetic_diseases|Jalili_syndrome|not_provided": 1,
    "Jalili_syndrome|not_provided|Retinal_dystrophy": 2,
    "CNNM4-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Jalili_syndrome|not_provided": 3,
    "Jalili_syndrome|CNNM4-related_disorder|not_specified|not_provided": 1,
    "Jalili_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Jalili_syndrome|not_specified|not_provided": 1,
    "not_provided|Jalili_syndrome|Retinitis_pigmentosa": 1,
    "Oligosynaptic_infertility|Acromesomelic_dysplasia_2B": 1,
    "Duane_retraction_syndrome": 12,
    "Duane_retraction_syndrome|not_specified": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency": 21,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|not_specified|not_provided": 2,
    "not_provided|Combined_immunodeficiency_due_to_ZAP70_deficiency": 2,
    "ZAP70-Related_Severe_Combined_Immunodeficiency": 339,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-Related_Severe_Combined_Immunodeficiency": 9,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2": 1,
    "not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency|not_specified|Combined_immunodeficiency_due_to_ZAP70_deficiency": 3,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Severe_combined_immunodeficiency_disease": 1,
    "ZAP70-related_disorder|ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Inborn_genetic_diseases|not_provided": 1,
    "Combined_immunodeficiency": 3,
    "not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency": 5,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency": 8,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Inborn_genetic_diseases": 10,
    "Autoimmune_disease|_multisystem|_infantile-onset|_2": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided|not_specified": 2,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|Combined_immunodeficiency_due_to_ZAP70_deficiency": 1,
    "Inborn_genetic_diseases|ZAP70-Related_Severe_Combined_Immunodeficiency": 8,
    "not_provided|Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-related_disorder|ZAP70-Related_Severe_Combined_Immunodeficiency|not_specified": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_specified|not_provided|Combined_immunodeficiency_due_to_ZAP70_deficiency": 2,
    "not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency|ZAP70-related_disorder": 1,
    "Combined_immunodeficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-Related_Severe_Combined_Immunodeficiency": 1,
    "Inborn_genetic_diseases|not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency": 2,
    "not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency": 1,
    "Autoimmune_disease|_multisystem|_infantile-onset|_2|ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided": 1,
    "ZAP70-related_disorder|ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2": 1,
    "not_specified|ZAP70-Related_Severe_Combined_Immunodeficiency": 3,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_specified": 2,
    "not_specified|ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency": 1,
    "not_specified|not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|ZAP70-Related_Severe_Combined_Immunodeficiency": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided": 6,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided|Combined_immunodeficiency_due_to_ZAP70_deficiency": 1,
    "Autoimmune_disease|_multisystem|_infantile-onset|_2|Combined_immunodeficiency_due_to_ZAP70_deficiency|Inborn_genetic_diseases|ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided": 1,
    "not_provided|Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-related_disorder|ZAP70-Related_Severe_Combined_Immunodeficiency": 1,
    "Combined_immunodeficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|Combined_immunodeficiency_due_to_ZAP70_deficiency": 1,
    "Autoimmune_disease|_multisystem|_infantile-onset|_2|Combined_immunodeficiency_due_to_ZAP70_deficiency|not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency": 1,
    "ZAP70-related_disorder": 3,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|ZAP70-related_disorder": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|not_specified": 1,
    "Severe_combined_immunodeficiency_disease|ZAP70-Related_Severe_Combined_Immunodeficiency": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-related_disorder|ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided|not_specified": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-Related_Severe_Combined_Immunodeficiency|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided": 1,
    "not_specified|not_provided|ZAP70-Related_Severe_Combined_Immunodeficiency|ZAP70-related_disorder": 1,
    "ZAP70-related_disorder|ZAP70-Related_Severe_Combined_Immunodeficiency": 2,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided|Combined_immunodeficiency_due_to_ZAP70_deficiency|ZAP70-related_disorder": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency|not_provided|ZAP70-related_disorder|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|Autoimmune_disease|_multisystem|_infantile-onset|_2|Inborn_genetic_diseases|ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|Combined_immunodeficiency_due_to_ZAP70_deficiency|not_provided": 1,
    "ZAP70-Related_Severe_Combined_Immunodeficiency|not_provided|Inborn_genetic_diseases": 1,
    "Combined_immunodeficiency_due_to_ZAP70_deficiency|not_provided": 1,
    "VWA3B-related_disorder": 14,
    "Spinocerebellar_ataxia|_autosomal_recessive_22": 6,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive_22": 1,
    "not_provided|VWA3B-related_disorder": 4,
    "Spinocerebellar_ataxia|_autosomal_recessive_22|not_provided": 3,
    "Spinocerebellar_ataxia|_autosomal_recessive_22|not_specified": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_22": 1,
    "VWA3B-related_disorder|not_provided": 2,
    "Achromatopsia_2": 93,
    "not_provided|Achromatopsia_2": 31,
    "Achromatopsia|not_provided|Achromatopsia_2": 1,
    "Achromatopsia_2|not_provided|CNGA3-related_disorder": 2,
    "not_provided|Achromatopsia|Achromatopsia_2": 1,
    "not_provided|Achromatopsia_2|not_specified": 2,
    "Inborn_genetic_diseases|Achromatopsia_2|not_provided": 1,
    "not_provided|Achromatopsia_2|CNGA3-related_disorder|Cone-rod_dystrophy": 1,
    "not_provided|Abnormality_of_the_eye": 1,
    "Achromatopsia_2|not_provided|CNGA3-related_retinopathy": 1,
    "Achromatopsia|Achromatopsia_2": 1,
    "Achromatopsia_2|not_provided": 28,
    "CNGA3-related_disorder|not_specified|not_provided|Achromatopsia_2": 1,
    "Inborn_genetic_diseases|Achromatopsia_2": 1,
    "Achromatopsia_2|not_specified|not_provided": 1,
    "CNGA3-related_disorder|not_provided": 6,
    "Retinal_dystrophy|not_provided|Achromatopsia_2": 6,
    "Achromatopsia_2|not_provided|Retinal_dystrophy": 1,
    "maculopathy": 2,
    "Achromatopsia_2|Retinal_dystrophy|not_provided": 3,
    "CNGA3-related_disorder|Achromatopsia_2|Inborn_genetic_diseases|not_provided": 1,
    "CNGA3-related_disorder|Achromatopsia_2|not_provided": 2,
    "CNGA3-related_retinopathy": 2,
    "not_provided|Achromatopsia_2|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_specified|not_provided|Achromatopsia_2": 2,
    "Achromatopsia_2|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Achromatopsia_2|CNGA3-related_disorder": 1,
    "Retinal_dystrophy|Achromatopsia|Achromatopsia_2": 1,
    "not_provided|CNGA3-related_disorder|Achromatopsia_2": 3,
    "not_provided|CNGA3-related_disorder": 2,
    "not_provided|CNGA3-related_retinopathy": 2,
    "Inborn_genetic_diseases|Achromatopsia_2|not_provided|Achromatopsia": 1,
    "Retinal_dystrophy|CNGA3-related_disorder|not_provided|Achromatopsia_2|Achromatopsia": 1,
    "Achromatopsia_2|Retinal_dystrophy": 3,
    "not_provided|Achromatopsia|Retinal_dystrophy|Achromatopsia_2|not_specified": 1,
    "CNGA3-related_disorder|Retinal_dystrophy|not_provided|Achromatopsia_2": 1,
    "Retinal_dystrophy|Achromatopsia_2|not_provided": 3,
    "Retinal_dystrophy|Achromatopsia|CNGA3-related_disorder|not_provided|Achromatopsia_2": 1,
    "Achromatopsia_2|Achromatopsia|not_provided": 2,
    "Optic_atrophy|Retinal_dystrophy|Achromatopsia|not_provided|Achromatopsia_2|Macular_degeneration|Photophobia|Color_vision_defect": 1,
    "Achromatopsia|Achromatopsia_2|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Achromatopsia_2|Monochromacy": 1,
    "Retinal_dystrophy|Achromatopsia|not_provided|Achromatopsia_2": 2,
    "Achromatopsia|not_provided|CNGA3-related_disorder|Retinal_dystrophy": 1,
    "not_provided|Achromatopsia_2|Retinal_dystrophy|Achromatopsia": 1,
    "Retinal_dystrophy|Achromatopsia_2|Cone_dystrophy|not_provided": 1,
    "CNGA3-related_disorder|not_provided|not_specified": 1,
    "CNGA3-related_disorder|Achromatopsia_2|Achromatopsia|not_provided": 1,
    "not_specified|Achromatopsia_2|not_provided": 1,
    "Achromatopsia_2|Abnormality_of_the_eye|not_provided|Achromatopsia|Macular_dystrophy|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Achromatopsia_2|Achromatopsia_3": 1,
    "not_provided|Retinal_dystrophy|Achromatopsia_2": 2,
    "not_provided|Cone_dystrophy": 4,
    "CNGA3-related_retinopathy|CNGA3-related_disorder|Retinal_dystrophy|Achromatopsia|not_provided|Achromatopsia_2|Achromatopsia_3": 1,
    "Achromatopsia|Retinal_dystrophy|not_provided|CNGA3-related_disorder|Achromatopsia_2": 1,
    "Retinal_dystrophy|Achromatopsia|not_provided|Achromatopsia_2|Monochromacy": 1,
    "not_provided|Achromatopsia_2|Achromatopsia": 1,
    "Inborn_genetic_diseases|Achromatopsia_2|Retinal_dystrophy|Achromatopsia|not_provided|not_specified": 1,
    "Achromatopsia_2|not_provided|Abnormality_of_the_eye|Retinal_dystrophy": 1,
    "not_provided|CNGA3-related_disorder|Retinal_dystrophy|Achromatopsia_2": 1,
    "not_provided|Achromatopsia_2|Retinal_dystrophy": 1,
    "Retinal_disorders": 6,
    "not_provided|Retinal_dystrophy|Achromatopsia": 1,
    "not_specified|Achromatopsia": 2,
    "Achromatopsia_2|not_provided|not_specified": 1,
    "CNGA3-related_disorder": 1,
    "not_provided|Achromatopsia|Retinal_dystrophy": 2,
    "not_provided|CNGA3-related_retinopathy|Achromatopsia_2": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1": 325,
    "NEURODEVELOPMENTAL_DISORDER_WITH_GROWTH_IMPAIRMENT|_QUADRIPARESIS|_AND_POOR_OR_ABSENT_SPEECH": 5,
    "Pectus_excavatum|Nystagmus|Hypotonia|visual_disturbance|Microcephaly|NEURODEVELOPMENTAL_DISORDER_WITH_GROWTH_IMPAIRMENT|_QUADRIPARESIS|_AND_POOR_OR_ABSENT_SPEECH": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_3": 1,
    "UNC50-related_disorder": 6,
    "not_provided|TSGA10-related_disorder": 3,
    "TSGA10-related_disorder": 4,
    "Spermatogenic_failure_26": 1,
    "LIPT1-related_disorder|not_provided": 2,
    "Lipoyl_transferase_1_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Lipoyl_transferase_1_deficiency|not_provided": 3,
    "Lipoyl_transferase_1_deficiency": 5,
    "Lipoyl_transferase_1_deficiency|See_cases": 1,
    "Leigh_syndrome|not_specified|Lipoyl_transferase_1_deficiency": 1,
    "Lipoyl_transferase_1_deficiency|not_specified|Leigh_syndrome|Hearing_impairment|Hypotonia|Abnormal_optic_nerve_morphology|Abnormal_cardiovascular_system_morphology|Failure_to_thrive|not_provided": 1,
    "not_provided|LIPT1-related_disorder|Inborn_genetic_diseases": 1,
    "Lipoyl_transferase_1_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Lipoyl_transferase_1_deficiency|not_provided": 1,
    "not_specified|LIPT1-related_disorder|not_provided": 1,
    "Lipoyl_transferase_1_deficiency|not_specified|not_provided": 1,
    "not_provided|LIPT1-related_disorder": 2,
    "LIPT1-related_disorder": 2,
    "Large_for_gestational_age|Preeclampsia": 1,
    "not_provided|not_specified|AFF3-related_disorder": 1,
    "AFF3-related_disorder": 27,
    "not_provided|AFF3-related_disorder": 5,
    "Inborn_genetic_diseases|KINSSHIP_syndrome": 3,
    "AFF3-related_disorder|Inborn_genetic_diseases": 2,
    "AFF3-related_disorder|not_provided": 6,
    "Inborn_genetic_diseases|AFF3-related_disorder": 1,
    "KINSSHIP_syndrome": 13,
    "KINSSHIP_syndrome|AFF3-related_disorder": 1,
    "AFF3-associated_disorder": 1,
    "KINSSHIP_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|KINSSHIP_syndrome": 1,
    "AFF3-related_neurodevelopmental_disorders|KINSSHIP_syndrome": 1,
    "NPAS2-related_disorder": 2,
    "not_provided|NPAS2-related_disorder": 1,
    "NPAS2-related_disorder|not_provided": 1,
    "not_provided|RPL31-related_condition": 1,
    "RPL31-related_condition": 1,
    "MAP4K4-related_neurodevelopmental_delay": 1,
    "MAP4K4-related_autism_spectrum_disorder": 1,
    "Imperforate_anus|Renal_dysplasia": 1,
    "Ascending_aortic_dissection": 19,
    "Chronic_recurrent_multifocal_osteomyelitis_3": 1,
    "not_provided|Behcet_disease": 1,
    "Behcet_disease": 10,
    "Acute_megakaryoblastic_leukemia|Mediastinal_germ_cell_tumor": 7,
    "not_provided|POU3F3-related_disorder": 4,
    "Snijders_blok-fisher_syndrome": 40,
    "POU3F3-related_disorder|Inborn_genetic_diseases": 1,
    "POU3F3-related_disorder": 10,
    "Inborn_genetic_diseases|Snijders_blok-fisher_syndrome": 2,
    "not_provided|Snijders_blok-fisher_syndrome": 2,
    "GPR45-related_condition|not_provided": 2,
    "not_provided|Primary_dilated_cardiomyopathy|not_specified": 16,
    "Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy": 150,
    "not_specified|not_provided|Primary_dilated_cardiomyopathy": 18,
    "Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy": 2,
    "Primary_dilated_cardiomyopathy|not_provided|not_specified": 14,
    "not_specified|Primary_dilated_cardiomyopathy|not_provided": 6,
    "not_specified|FHL2-related_disorder|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|FHL2-related_disorder": 2,
    "Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|not_specified|FHL2-related_disorder": 1,
    "not_specified|Primary_dilated_cardiomyopathy|FHL2-related_disorder": 1,
    "FHL2-related_disorder|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified": 2,
    "Cardiomyopathy|FHL2-related_disorder|Primary_dilated_cardiomyopathy|not_specified": 1,
    "not_specified|not_provided|FHL2-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|FHL2-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided": 2,
    "not_specified|Cardiomyopathy|FHL2-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "FHL2-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "FHL2-related_disorder": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 211,
    "Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 146,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|SLC5A7-related_disorder|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 1,
    "Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|Inborn_genetic_diseases": 10,
    "Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|not_provided": 6,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 5,
    "not_provided|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 4,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|not_provided": 3,
    "Congenital_myasthenic_syndrome_20": 7,
    "Neuronopathy|_distal_hereditary_motor|_type_7A": 5,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 13,
    "Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|Inborn_genetic_diseases": 7,
    "SLC5A7-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|not_provided": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|not_specified": 1,
    "Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|not_provided": 6,
    "SLC5A7-related_disorder|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 3,
    "Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|SLC5A7-related_disorder": 1,
    "not_provided|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 5,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 2,
    "SLC5A7-related_disorder|not_provided|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 2,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|Inborn_genetic_diseases": 2,
    "not_provided|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|Inborn_genetic_diseases": 3,
    "not_specified|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|not_provided": 1,
    "Congenital_myasthenic_syndrome_20|not_provided|Neuronopathy|_distal_hereditary_motor|_type_7A": 1,
    "not_provided|SLC5A7-related_disorder|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|not_specified": 1,
    "not_provided|SLC5A7-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|Inborn_genetic_diseases": 1,
    "SLC5A7-related_disorder|not_provided": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20": 1,
    "SLC5A7-related_disorder|not_provided|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A": 1,
    "Congenital_myasthenic_syndrome_20|Neuronopathy|_distal_hereditary_motor|_type_7A|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|SLC5A7-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_7A": 1,
    "Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_7A|Congenital_myasthenic_syndrome_20|Inborn_genetic_diseases": 1,
    "GCC2-related_disorder|not_specified": 2,
    "GCC2-related_disorder|not_provided": 4,
    "GCC2-related_disorder": 11,
    "not_provided|GCC2-related_disorder": 1,
    "not_specified|Familial_acute_necrotizing_encephalopathy|not_provided": 9,
    "Familial_acute_necrotizing_encephalopathy": 571,
    "Familial_acute_necrotizing_encephalopathy|not_provided|not_specified": 4,
    "not_provided|not_specified|Familial_acute_necrotizing_encephalopathy": 13,
    "Familial_acute_necrotizing_encephalopathy|not_specified": 45,
    "not_specified|Familial_acute_necrotizing_encephalopathy": 50,
    "not_provided|Familial_acute_necrotizing_encephalopathy": 48,
    "Familial_acute_necrotizing_encephalopathy|not_specified|not_provided": 7,
    "not_specified|not_provided|Familial_acute_necrotizing_encephalopathy": 12,
    "not_provided|Familial_acute_necrotizing_encephalopathy|not_specified": 9,
    "Familial_acute_necrotizing_encephalopathy|not_provided": 37,
    "not_provided|Familial_acute_necrotizing_encephalopathy|See_cases": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 2,
    "Susceptibility_to_HIV_infection": 14,
    "not_provided|Familial_acute_necrotizing_encephalopathy|RANBP2-related_disorder": 1,
    "RANBP2-related_disorder": 9,
    "Familial_acute_necrotizing_encephalopathy|RANBP2-related_disorder": 3,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_specified|Familial_acute_necrotizing_encephalopathy": 1,
    "RANBP2-related_disorder|Familial_acute_necrotizing_encephalopathy": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant": 8,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia|not_provided": 4,
    "Hypohidrotic_ectodermal_dysplasia|Hypohidrotic_Ectodermal_Dysplasia|_Dominant": 10,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia": 14,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|not_provided|Hypohidrotic_ectodermal_dysplasia": 1,
    "not_provided|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Hypohidrotic_ectodermal_dysplasia|not_provided": 1,
    "EDAR-related_disorder": 5,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 56,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 45,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|not_provided": 4,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Oligodontia": 1,
    "Ectodermal_dysplasia_11B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|not_provided|Ectodermal_dysplasia_10a|_hypohidrotic/hair/tooth_type|_autosomal_dominant": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia": 1,
    "not_provided|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_specified|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia|Non-syndromic_oligodontia": 1,
    "not_provided|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 3,
    "EDAR-related_disorder|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 1,
    "not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 3,
    "Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Hair_morphology_1|_hair_thickness|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|not_provided|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia|not_specified|Non-syndromic_oligodontia": 1,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Non-syndromic_oligodontia|not_provided|Ectodermal_dysplasia_10a|_hypohidrotic/hair/tooth_type|_autosomal_dominant": 1,
    "Ectodermal_dysplasia_10a|_hypohidrotic/hair/tooth_type|_autosomal_dominant": 1,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 2,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_specified|Hypohidrotic_ectodermal_dysplasia|not_provided": 2,
    "not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 2,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|not_specified|not_provided": 1,
    "Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 3,
    "not_provided|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|not_specified|Hypohidrotic_ectodermal_dysplasia": 1,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|not_provided": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Non-syndromic_oligodontia": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|HAIR_MORPHOLOGY_1|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_provided|not_specified|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 1,
    "not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia": 1,
    "Ectodermal_dysplasia|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Hypohidrotic_ectodermal_dysplasia|Inborn_genetic_diseases": 1,
    "not_provided|Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 1,
    "Hypohidrotic_ectodermal_dysplasia|EDAR-related_disorder|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 1,
    "not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|HAIR_MORPHOLOGY_1|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Inborn_genetic_diseases|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Hypohidrotic_ectodermal_dysplasia": 1,
    "Inborn_genetic_diseases|not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia|Hypohidrotic_Ectodermal_Dysplasia|_Dominant": 1,
    "Ectodermal_dysplasia": 3,
    "Hypohidrotic_ectodermal_dysplasia|not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "Non-syndromic_oligodontia": 2,
    "not_specified|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|not_provided": 1,
    "Oligodontia|Ectodermal_dysplasia|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia|Non-syndromic_oligodontia|not_specified": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|not_provided": 1,
    "Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|not_provided|Ectodermal_dysplasia_10a|_hypohidrotic/hair/tooth_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 1,
    "Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Hypohidrotic_ectodermal_dysplasia|not_provided|EDAR-related_disorder": 1,
    "not_provided|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Hypohidrotic_ectodermal_dysplasia": 1,
    "Hypohidrotic_ectodermal_dysplasia|not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Hypohidrotic_Ectodermal_Dysplasia|_Dominant|Hypohidrotic_ectodermal_dysplasia": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|not_provided": 1,
    "Inborn_genetic_diseases|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Ectodermal_dysplasia_10B|_hypohidrotic/hair/tooth_type|_autosomal_recessive": 1,
    "Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Inborn_genetic_diseases|Hypohidrotic_ectodermal_dysplasia|EDAR-related_disorder|Hypohidrotic_Ectodermal_Dysplasia|_Dominant": 1,
    "not_provided|Ectodermal_dysplasia_10A|_hypohidrotic/hair/nail_type|_autosomal_dominant|Autosomal_recessive_hypohidrotic_ectodermal_dysplasia_syndrome|Non-syndromic_oligodontia": 1,
    "Hypohidrotic_Ectodermal_Dysplasia|_Dominant|not_provided": 1,
    "Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect": 3,
    "Nephronophthisis|Joubert_syndrome|Renal_dysplasia_and_retinal_aplasia": 1,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1": 2,
    "Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1": 61,
    "Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect": 2,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 5,
    "NPHP1-related_disorder|not_provided": 1,
    "NPHP1-related_disorder": 13,
    "not_provided|Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|Inborn_genetic_diseases": 1,
    "NPHP1-related_disorder|Nephronophthisis": 15,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Nephronophthisis|NPHP1-related_disorder": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|Inborn_genetic_diseases": 1,
    "NPHP1-related_disorder|Nephronophthisis|not_provided": 3,
    "Joubert_syndrome_with_renal_defect": 28,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 7,
    "Nephronophthisis|Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect": 1,
    "Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|Nephronophthisis": 4,
    "Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis|Nephronophthisis_1|not_provided|NPHP1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Nephronophthisis": 2,
    "Joubert_syndrome_with_renal_defect|Nephronophthisis": 4,
    "Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1": 9,
    "NPHP1-related_disorder|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "NPHP1-related_disorder|Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|not_provided": 1,
    "not_specified|Nephronophthisis|not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1": 5,
    "Nephronophthisis|Inborn_genetic_diseases|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|not_provided": 1,
    "Nephronophthisis|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|not_provided|NPHP1-related_disorder|Inborn_genetic_diseases": 1,
    "NPHP1-related_disorder|Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1": 3,
    "not_provided|NPHP1-related_disorder": 2,
    "Nephronophthisis_1": 10,
    "Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis|NPHP1-related_disorder": 1,
    "NPHP1-related_disorder|Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|NPHP1-related_disorder": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis": 3,
    "Nephronophthisis|NPHP1-related_disorder": 7,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Nephronophthisis|Senior-Loken_syndrome_1": 1,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Nephronophthisis": 2,
    "not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|Nephronophthisis": 2,
    "Nephronophthisis|Inborn_genetic_diseases|NPHP1-related_disorder|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Nephronophthisis": 2,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|not_provided|Nephronophthisis": 3,
    "not_provided|NPHP1-related_disorder|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|NPHP1-related_disorder|Senior-Loken_syndrome_1|Nephronophthisis": 1,
    "not_provided|Joubert_syndrome_with_renal_defect|NPHP1-related_disorder|Joubert_syndrome_and_related_disorders|Nephronophthisis|Senior-Loken_syndrome_1|Nephronophthisis_1": 1,
    "Retinal_dystrophy|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|NPHP1-related_disorder": 3,
    "Nephronophthisis|NPHP1-related_disorder|not_provided": 3,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|NPHP1-related_disorder|not_specified|Nephronophthisis": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 2,
    "Joubert_syndrome_with_renal_defect|Nephronophthisis|Senior-Loken_syndrome_1|not_provided|Nephronophthisis_1|not_specified": 1,
    "not_provided|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis|NPHP1-related_disorder|Nephronophthisis_1|not_specified": 1,
    "Bardet-Biedl_syndrome_1|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis|NPHP1-related_disorder|Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|not_provided": 1,
    "Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|Nephronophthisis": 8,
    "not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|NPHP1-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect": 4,
    "Nephronophthisis_1|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|not_provided": 1,
    "Nephronophthisis|not_specified|not_provided|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect": 1,
    "Nephronophthisis|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect": 2,
    "Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 3,
    "Nephronophthisis|NPHP1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|not_provided": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis|Inborn_genetic_diseases": 2,
    "NPHP1-related_disorder|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1": 2,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|NPHP1-related_disorder|not_provided": 1,
    "NPHP1-related_disorder|Nephronophthisis_1|Nephronophthisis": 2,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_with_renal_defect": 1,
    "not_provided|NPHP1-related_disorder|Nephronophthisis|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1": 1,
    "Inborn_genetic_diseases|Kidney_disorder": 1,
    "not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis": 1,
    "not_provided|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|Nephronophthisis": 1,
    "NPHP1-related_disorder|Nephronophthisis|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1": 2,
    "NPHP1-related_disorder|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|Nephronophthisis|not_provided": 1,
    "not_provided|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect": 1,
    "not_specified|NPHP1-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Nephronophthisis|NPHP1-related_disorder|Inborn_genetic_diseases|not_provided|Retinal_dystrophy|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis|not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|not_specified": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|not_provided|NPHP1-related_disorder|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|NPHP1-related_disorder|Retinal_dystrophy|not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis|Retinal_dystrophy|not_provided": 1,
    "Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Joubert_syndrome_and_related_disorders|NPHP1-related_disorder": 1,
    "Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_specified|NPHP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_provided|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis_1|NPHP1-related_disorder": 1,
    "Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|not_provided|not_specified|NPHP1-related_disorder|Nephronophthisis": 1,
    "not_specified|Nephronophthisis|not_provided": 1,
    "not_specified|Nephronophthisis|Senior-Loken_syndrome_1|not_provided|Joubert_syndrome_with_renal_defect|Nephronophthisis_1": 1,
    "Nephronophthisis|Inborn_genetic_diseases|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "NPHP1-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Retinal_dystrophy|not_provided": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|not_provided": 2,
    "Kidney_disorder|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis|not_specified|not_provided": 1,
    "Retinal_dystrophy|Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "not_provided|not_specified|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Nephronophthisis": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Renal_dysplasia_and_retinal_aplasia|Joubert_syndrome|Nephronophthisis|NPHP1-related_disorder|not_provided": 1,
    "NPHP1-related_disorder|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|not_specified|Leber_congenital_amaurosis|Nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|NPHP1-related_disorder|Nephronophthisis": 1,
    "Senior-Loken_syndrome_1": 1,
    "NPHP1-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|NPHP1-related_disorder": 1,
    "Nephronophthisis|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1": 1,
    "NPHP1-related_disorder|not_provided|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Nephronophthisis|Senior-Loken_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "NPHP1-related_disorder|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|NPHP1-related_disorder|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect": 1,
    "not_provided|Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_with_renal_defect|Nephronophthisis|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|NPHP1-related_disorder|not_provided|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|NPHP1-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis_1|not_provided|Nephronophthisis|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect": 1,
    "Inborn_genetic_diseases|NPHP1-related_disorder|Nephronophthisis|not_specified|not_provided": 1,
    "Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|NPHP1-related_disorder|Inborn_genetic_diseases|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|NPHP1-related_disorder": 1,
    "not_provided|NPHP1-related_disorder|Nephronophthisis|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1": 1,
    "Joubert_syndrome_with_renal_defect|not_provided|Joubert_syndrome_and_related_disorders|Nephronophthisis|Nephronophthisis_1|Senior-Loken_syndrome_1": 1,
    "Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Senior-Loken_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|NPHP1-related_disorder|Nephronophthisis": 1,
    "NPHP1-related_disorder|Nephronophthisis|not_specified|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|not_provided": 1,
    "Nephronophthisis|Joubert_syndrome_and_related_disorders|Joubert_syndrome_with_renal_defect": 1,
    "Nephronophthisis_1|Joubert_syndrome_with_renal_defect|Senior-Loken_syndrome_1|Nephronophthisis|not_provided": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|not_provided": 1,
    "not_specified|Nephronophthisis|not_provided|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1": 1,
    "Nephronophthisis|Nephronophthisis_1": 1,
    "Nephronophthisis_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis": 1,
    "Nephronophthisis|Senior-Loken_syndrome_1|Nephronophthisis_1|Joubert_syndrome_with_renal_defect|NPHP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|not_provided|NPHP1-related_disorder": 1,
    "Intellectual_disability|_X-linked_102|Nephronophthisis|not_specified|not_provided|Joubert_syndrome_1|Senior-Loken_syndrome_1|Joubert_syndrome_with_renal_defect|Nephronophthisis_1": 1,
    "BUB1-related_disorder|not_specified|not_provided": 2,
    "Microcephaly_30|_primary|_autosomal_recessive": 4,
    "BUB1-related_disorder|not_provided": 3,
    "not_specified|BUB1-related_disorder|not_provided": 2,
    "Colorectal_cancer_with_chromosomal_instability|_somatic": 2,
    "not_provided|not_specified|BUB1-related_disorder": 1,
    "BUB1-related_disorder|not_provided|not_specified": 1,
    "BUB1-related_disorder": 1,
    "Microcephaly_30|_primary|_autosomal_recessive|not_provided": 1,
    "BCL2L11-related_condition": 1,
    "Rothmund-Thomson_syndrome_type_1|not_provided": 4,
    "not_provided|Rothmund-Thomson_syndrome_type_1": 3,
    "Rothmund-Thomson_syndrome_type_2": 5,
    "Rothmund-Thomson_syndrome_type_1": 4,
    "not_provided|Rothmund-Thomson_syndrome_type_1|not_specified": 1,
    "not_specified|Rothmund-Thomson_syndrome_type_1|not_provided": 1,
    "not_specified|Rothmund-Thomson_syndrome_type_1": 1,
    "Retinitis_pigmentosa_38": 25,
    "MERTK-related_disorder|not_provided": 5,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_38": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_38": 2,
    "not_provided|Retinitis_pigmentosa|Optic_atrophy": 1,
    "not_provided|Retinitis_pigmentosa|MERTK-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_38": 1,
    "not_provided|Retinitis_pigmentosa_38|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_38": 13,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_38|not_provided": 3,
    "not_provided|MERTK-related_disorder": 3,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_38|MERTK-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_38": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_38": 1,
    "Retinitis_pigmentosa_38|not_provided": 6,
    "Retinal_dystrophy|Retinitis_pigmentosa|MERTK-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_38|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_38": 3,
    "MERTK-related_disorder": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_38|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|MERTK-related_disorder": 2,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_38": 1,
    "Retinitis_pigmentosa_38|MERTK-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_38|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_38": 1,
    "not_provided|Inborn_genetic_diseases|MERTK-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_38|not_provided": 3,
    "Retinitis_pigmentosa_38|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|not_provided": 8,
    "Retinitis_pigmentosa_38|not_provided|Retinitis_pigmentosa": 2,
    "not_provided|Retinitis_pigmentosa_38|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_38": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_38": 2,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_38|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_38|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|Optic_atrophy|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa": 31,
    "Retinitis_Pigmentosa|_Recessive|not_provided": 21,
    "Retinitis_pigmentosa|Inborn_genetic_diseases": 6,
    "not_provided|Retinitis_pigmentosa_38|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa|Inborn_genetic_diseases|Retinitis_pigmentosa_38": 1,
    "not_provided|Retinitis_pigmentosa_38|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_38|Retinal_dystrophy|not_provided": 2,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_38|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_38|not_specified|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_38|MERTK-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_38": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_38": 1,
    "MERTK-related_disorder|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_38": 1,
    "Inborn_genetic_diseases|MERTK-related_disorder|not_provided": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_38|not_provided": 1,
    "POLR1B-related_disorder": 5,
    "Treacher_Collins_syndrome_4": 6,
    "Treacher_Collins_syndrome_4|Treacher_Collins_syndrome": 2,
    "not_provided|POLR1B-related_disorder": 2,
    "POLR1B-related_disorder|Treacher_Collins_syndrome_4|Treacher_Collins_syndrome": 1,
    "not_specified|POLR1B-related_disorder": 1,
    "SLC20A1-related_disorder": 5,
    "Filippi_syndrome|not_provided": 5,
    "not_provided|CKAP2L-related_disorder": 4,
    "Filippi_syndrome": 16,
    "CKAP2L-related_disorder": 5,
    "not_provided|Filippi_syndrome": 5,
    "Intellectual_disability|Hypogonadism": 1,
    "Filippi_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Filippi_syndrome": 1,
    "Inborn_genetic_diseases|CKAP2L-related_disorder": 1,
    "CKAP2L-related_disorder|not_provided": 4,
    "IL1A-related_disorder": 5,
    "Cholangiocarcinoma|Endometriosis|IL1B-related_disorder|Antisynthetase_syndrome": 1,
    "IL1B-related_disorder": 1,
    "Coronary_heart_disease|_susceptibility_to|_2": 1,
    "Gastric_cancer_susceptibility_after_h._pylori_infection": 1,
    "Antisynthetase_syndrome": 2,
    "Inflammatory_bowel_disease_(infantile_ulcerative_colitis)_31|_autosomal_recessive": 1,
    "Generalized_pustular_psoriasis": 126,
    "Acrodermatitis_continua_suppurativa_of_Hallopeau": 6,
    "Generalized_pustular_psoriasis|Autoinflammatory_syndrome|not_provided": 1,
    "Generalized_pustular_psoriasis|Acrodermatitis_continua_suppurativa_of_Hallopeau": 1,
    "Generalized_pustular_psoriasis|Autoinflammatory_syndrome": 8,
    "Generalized_pustular_psoriasis|Acrodermatitis_continua_suppurativa_of_Hallopeau|not_provided": 4,
    "Acrodermatitis_continua_suppurativa_of_Hallopeau|Generalized_pustular_psoriasis": 2,
    "Generalized_pustular_psoriasis|not_provided|Autoinflammatory_syndrome": 1,
    "Acrodermatitis_continua_suppurativa_of_Hallopeau|Autoinflammatory_syndrome|IL36RN-related_disorder|not_provided|Generalized_pustular_psoriasis": 1,
    "Inborn_genetic_diseases|Generalized_pustular_psoriasis": 2,
    "Generalized_pustular_psoriasis|not_provided": 8,
    "Generalized_pustular_psoriasis|not_provided|Acrodermatitis_continua_suppurativa_of_Hallopeau|Autoinflammatory_syndrome": 1,
    "IL36RN-related_disorder|Acrodermatitis_continua_suppurativa_of_Hallopeau|not_provided|Generalized_pustular_psoriasis": 1,
    "not_provided|Autoinflammatory_syndrome|Generalized_pustular_psoriasis": 1,
    "Generalized_pustular_psoriasis|Inborn_genetic_diseases": 3,
    "Acrodermatitis_continua_suppurativa_of_Hallopeau|not_provided|Generalized_pustular_psoriasis": 3,
    "not_provided|Generalized_pustular_psoriasis|Autoinflammatory_syndrome": 2,
    "IL36RN-related_disorder|Generalized_pustular_psoriasis": 2,
    "Autoinflammatory_syndrome|Generalized_pustular_psoriasis": 3,
    "Acrodermatitis_continua_suppurativa_of_Hallopeau|not_provided": 1,
    "Generalized_pustular_psoriasis|Acrodermatitis_continua_suppurativa_of_Hallopeau|Autoinflammatory_syndrome|not_provided|IL36RN-related_disorder": 1,
    "IL36RN-related_disorder|Autoinflammatory_syndrome|Generalized_pustular_psoriasis": 1,
    "Deficiency_of_the_interleukin-36_receptor_antagonist|Generalized_pustular_psoriasis|not_provided": 1,
    "not_provided|Generalized_pustular_psoriasis": 7,
    "not_provided|Generalized_pustular_psoriasis|Acrodermatitis_continua_suppurativa_of_Hallopeau": 1,
    "not_provided|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|not_specified": 4,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 141,
    "Autoinflammatory_syndrome|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 4,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Microvascular_complications_of_diabetes|_susceptibility_to|_4|Gastric_cancer": 3,
    "IL1RN-related_disorder": 2,
    "Interstitial_lung_disease_2|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Microvascular_complications_of_diabetes|_susceptibility_to|_4|Gastric_cancer|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Gastric_cancer|Microvascular_complications_of_diabetes|_susceptibility_to|_4|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Autoinflammatory_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Inborn_genetic_diseases": 5,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|not_provided": 5,
    "not_provided|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 4,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Autoinflammatory_syndrome|not_specified|not_provided": 1,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Autoinflammatory_syndrome": 3,
    "not_provided|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Autoinflammatory_syndrome": 2,
    "Gastric_cancer_susceptibility_after_h._pylori_infection|Microvascular_complications_of_diabetes|_susceptibility_to|_4": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_4|Gastric_cancer|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "IL1RN-related_disorder|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|Autoinflammatory_syndrome|not_provided": 4,
    "not_specified|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Autoinflammatory_syndrome|IL1RN-related_disorder|not_provided|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Inborn_genetic_diseases|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|not_specified|not_provided": 2,
    "Autoinflammatory_syndrome|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis|not_provided": 1,
    "not_provided|not_specified|Sterile_multifocal_osteomyelitis_with_periostitis_and_pustulosis": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_2": 82,
    "Hypothyroidism|_congenital|_nongoitrous|_2|not_provided": 17,
    "not_provided|Hypothyroidism|_congenital|_nongoitrous|_2": 10,
    "not_specified|not_provided|Hypothyroidism|_congenital|_nongoitrous|_2": 1,
    "Inborn_genetic_diseases|not_provided|Hypothyroidism|_congenital|_nongoitrous|_2": 2,
    "Hypothyroidism|_congenital|_nongoitrous|_2|not_provided|not_specified": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_2|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|PAX8-related_disorder|Hypothyroidism|_congenital|_nongoitrous|_2|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Hypothyroidism|_congenital|_nongoitrous|_2|Intellectual_disability": 1,
    "not_provided|not_specified|Hypothyroidism|_congenital|_nongoitrous|_2": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_2|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Hypothyroidism|_congenital|_nongoitrous|_2": 2,
    "not_specified|Inborn_genetic_diseases|Hypothyroidism|_congenital|_nongoitrous|_2": 1,
    "PAX8-related_disorder|not_specified|not_provided|PAX8_POLYMORPHISM|Hypothyroidism|_congenital|_nongoitrous|_2": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_2|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hypothyroidism|_congenital|_nongoitrous|_2": 1,
    "PAX8-related_disorder|not_provided": 1,
    "not_provided|Hypothyroidism|_congenital|_nongoitrous|_2|Inborn_genetic_diseases": 1,
    "PAX8-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Hypothyroidism|_congenital|_nongoitrous|_2|not_provided": 1,
    "not_provided|PAX8-related_disorder": 1,
    "DPP10-related_disorder": 5,
    "CCDC93-related_condition": 1,
    "EN1-related_disorder": 2,
    "ENDOVE_syndrome|_limb-brain_type|EN1_syndrome": 1,
    "STEAP3-related_disorder": 5,
    "Severe_congenital_hypochromic_anemia_with_ringed_sideroblasts": 4,
    "Primary_ciliary_dyskinesia_15": 57,
    "not_provided|STEAP3-related_disorder": 6,
    "CFAP221-related_disorder": 2,
    "Young_syndrome": 2,
    "Primary_ciliary_dyskinesia|Young_syndrome": 2,
    "PTPN4-related_disorder": 10,
    "PTPN4-related_aberrant_neurodevelopment_and_growth": 1,
    "PTPN4-related_Neurodevelopmental_Disorder": 2,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|PTPN4-related_disorder": 1,
    "PTPN4-associated_disorder": 1,
    "GLI2-related_disorder": 63,
    "GLI2-related_disorder|not_specified|not_provided|Holoprosencephaly_9": 1,
    "Holoprosencephaly_9": 54,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 173,
    "Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 10,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 138,
    "Inborn_genetic_diseases|GLI2-related_disorder|not_provided": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|GLI2-related_disorder": 10,
    "GLI2-related_disorder|not_provided": 2,
    "Holoprosencephaly_9|GLI2-related_disorder|not_provided": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 24,
    "Inborn_genetic_diseases|not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 2,
    "not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 14,
    "not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 8,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 12,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 6,
    "Holoprosencephaly_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_9": 2,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_provided": 8,
    "not_specified|GLI2-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|not_specified|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "Intellectual_disability|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|Inborn_genetic_diseases|GLI2-related_disorder": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Inborn_genetic_diseases": 14,
    "Downturned_corners_of_mouth|Sparse_and_thin_eyebrow|CNS_hypomyelination|Growth_delay|Abnormal_facial_shape|Abnormal_pinna_morphology|Secondary_microcephaly|Abnormal_optic_nerve_morphology|Microcephaly|Sparse_scalp_hair|Hypoplasia_of_the_corpus_callosum": 2,
    "not_provided|GLI2-related_disorder": 2,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|GLI2-related_disorder": 9,
    "GLI2-related_disorder|Inborn_genetic_diseases|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "not_specified|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 8,
    "Inborn_genetic_diseases|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|GLI2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 2,
    "GLI2-related_disorder|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 16,
    "not_specified|Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_specified": 7,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|Inborn_genetic_diseases|not_provided": 1,
    "GLI2-related_disorder|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 9,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|GLI2-related_disorder|not_provided": 2,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided|GLI2-related_disorder": 2,
    "Inborn_genetic_diseases|GLI2-related_disorder|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "Holoprosencephaly_9|not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified": 2,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_specified|not_provided": 4,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided|Holoprosencephaly_9|not_specified": 2,
    "Holoprosencephaly_9|not_provided": 5,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified|not_provided": 8,
    "Inborn_genetic_diseases|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 8,
    "Microform_holoprosencephaly|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "not_specified|not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 3,
    "not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|Inborn_genetic_diseases": 7,
    "not_specified|not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 3,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified|not_provided|Holoprosencephaly_9": 1,
    "not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|GLI2-related_disorder|Inborn_genetic_diseases": 1,
    "GLI2-related_disorder|Holoprosencephaly_9": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_9": 3,
    "Disorder_of_sexual_differentiation|GLI2-related_disorder": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "not_provided|GLI2-related_disorder|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 3,
    "Holoprosencephaly_9|GLI2-related_disorder": 1,
    "Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|GLI2-related_disorder|not_provided": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified": 6,
    "GLI2-related_disorder|not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_provided|Inborn_genetic_diseases": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "not_provided|not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|GLI2-related_disorder": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_provided|GLI2-related_disorder": 2,
    "GLI2-related_disorder|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided|not_specified": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_specified|not_provided|Anophthalmia-microphthalmia_syndrome|Bardet-Biedl_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "Holoprosencephaly_9|not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "GLI2-related_disorder|not_specified|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 3,
    "GLI2-related_disorder|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified|not_provided": 3,
    "GLI2-related_disorder|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 2,
    "GLI2-related_disorder|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided|not_specified": 1,
    "not_provided|Holoprosencephaly_9|Inborn_genetic_diseases|Holoprosencephaly_1|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_specified|GLI2-related_disorder": 1,
    "Cerebellar_cyst": 1,
    "not_specified|Holoprosencephaly_9": 1,
    "not_provided|GLI2-related_disorder|Pituitary_stalk_interruption_syndrome": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form": 2,
    "Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|GLI2-related_disorder": 1,
    "Hand_tremor|Cerebral_arteriovenous_malformation|Arteriovenous_malformation|Tremor|Secondary_microcephaly|Poor_speech|Deeply_set_eye|Intellectual_disability|Hyperactivity|Seizure|Exostoses": 1,
    "Holoprosencephaly_9|Inborn_genetic_diseases|not_provided|not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|GLI2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Microcephaly": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "GLI2-related_disorder|Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_provided|not_specified": 1,
    "Holoprosencephaly_9|Inborn_genetic_diseases": 1,
    "not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified|Inborn_genetic_diseases|GLI2-related_disorder": 1,
    "not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "GLI2-related_disorder|Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|GLI2-related_disorder|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "GLI2-related_disorder|not_specified|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "not_provided|Holoprosencephaly_9|GLI2-related_disorder|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "Inborn_genetic_diseases|GLI2-related_disorder": 2,
    "GLI2-related_disorder|not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified": 1,
    "not_provided|Limbal_dermoid|Tessier_cleft|Congenital_cleft_nose|Hypertelorism|Low-set_ears|Abnormal_frontal_bone_morphology|Pericallosal_lipoma|Skin_tags|Facial_asymmetry|Upper_eyelid_coloboma": 1,
    "not_specified|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_provided": 1,
    "Weaver_syndrome|not_specified": 9,
    "not_specified|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|not_provided": 2,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|GLI2-related_disorder|not_specified|not_provided": 1,
    "not_specified|GLI2-related_disorder|not_provided|Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "Holoprosencephaly_9|not_provided|Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "GLI2-related_disorder|not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "Holoprosencephaly_9|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|not_specified|not_provided|Partial_androgen_insensitivity_syndrome": 1,
    "Holoprosencephaly_9|not_specified|GLI2-related_disorder|Inborn_genetic_diseases|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "not_specified|GLI2-related_disorder|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9": 1,
    "not_provided|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Holoprosencephaly_9|GLI2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Holoprosencephaly_9|GLI2-related_disorder|Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome": 1,
    "not_provided|Holoprosencephaly_9": 4,
    "not_provided|Holoprosencephaly_sequence": 10,
    "CLASP1-related_disorder": 16,
    "not_provided|CLASP1-related_disorder": 4,
    "not_provided|RNU4ATAC-related_disorder|CLASP1-related_disorder": 2,
    "CLASP1-related_disorder|RNU4ATAC-related_disorder": 1,
    "Lowry-Wood_syndrome|not_provided": 1,
    "RNU4ATAC-related_spliceosomopathies|not_provided": 1,
    "Lowry-Wood_syndrome": 3,
    "not_provided|Roifman_syndrome": 2,
    "RNU4ATAC-related_disorder|Roifman_syndrome|Short_stature|Microcephaly|Neurodevelopmental_delay|Cardiomyopathy|Craniosynostosis_syndrome|not_specified|not_provided|Spondyloepiphyseal_dysplasia_congenita": 1,
    "CLASP1-related_disorder|Lowry-Wood_syndrome|Roifman_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|not_provided": 1,
    "Lowry-Wood_syndrome|Roifman_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|not_provided": 1,
    "not_provided|Lowry-Wood_syndrome|RNU4ATAC-related_disorder|Roifman_syndrome": 1,
    "Roifman_syndrome|not_provided": 2,
    "RNU4ATAC-related_disorder|CLASP1-related_disorder|not_provided": 1,
    "Osteodysplastic_primordial_dwarfism|_type_1": 2,
    "not_provided|Osteodysplastic_primordial_dwarfism|_type_1": 2,
    "CLASP1-related_disorder|RNU4ATAC-related_disorder|not_provided": 3,
    "RNU4ATAC-related_disorder|not_provided": 2,
    "RNU4ATAC_spectrum_disorder": 1,
    "CLASP1-related_disorder|RNU4ATAC-related_disorder|Lowry-Wood_syndrome|Roifman_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|not_provided|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Osteodysplastic_primordial_dwarfism|_type_1|Roifman_syndrome|not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "Roifman_syndrome|not_provided|Lowry-Wood_syndrome": 1,
    "Lowry-Wood_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|not_provided": 2,
    "Lowry-Wood_syndrome|Roifman_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|RNU4ATAC-related_spliceosomopathies|not_provided": 1,
    "Lowry-Wood_syndrome|Roifman_syndrome|not_provided|Osteodysplastic_primordial_dwarfism|_type_1": 1,
    "Lowry-Wood_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|Roifman_syndrome|RNU4ATAC-related_disorder|CLASP1-related_disorder|not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "RNU4ATAC_spectrum_disorder|not_provided|Osteodysplastic_primordial_dwarfism|_type_1": 1,
    "not_provided|Osteodysplastic_primordial_dwarfism|_type_1|Roifman_syndrome|Lowry-Wood_syndrome": 1,
    "Lowry-Wood_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|Roifman_syndrome|not_provided": 2,
    "not_provided|Osteodysplastic_primordial_dwarfism|_type_1|Lowry-Wood_syndrome|Roifman_syndrome": 1,
    "Osteodysplastic_primordial_dwarfism|_type_1|not_provided": 1,
    "not_provided|RNU4ATAC-related_disorder": 1,
    "Roifman_syndrome|Lowry-Wood_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|not_provided": 1,
    "CLASP1-related_disorder|not_provided": 1,
    "RNU4ATAC-related_disorder|Roifman_syndrome|not_provided": 1,
    "Osteodysplastic_primordial_dwarfism|_type_1|not_provided|Roifman_syndrome": 1,
    "Lowry-Wood_syndrome|Roifman_syndrome|Osteodysplastic_primordial_dwarfism|_type_1|CLASP1-related_disorder|not_provided": 1,
    "RNU4ATAC-related_disorder|CLASP1-related_disorder": 1,
    "CNTNAP5-related_disorder": 20,
    "CNTNAP5-related_disorder|not_provided": 10,
    "not_provided|CNTNAP5-related_disorder": 3,
    "not_specified|CNTNAP5-related_disorder": 1,
    "CNTNAP5-associated_intellectual_disability": 1,
    "Blood_group|_Gerbich_system": 3,
    "not_provided|GYPC-related_disorder": 2,
    "Glycophorin_c|_gerbich_variant|Malaria|_resistance_to": 1,
    "GYPC-related_disorder|not_provided": 2,
    "not_provided|Myopathy|_centronuclear|_2": 24,
    "Myopathy|_centronuclear|_2|not_provided": 31,
    "Myopathy|_centronuclear|_2": 509,
    "Inborn_genetic_diseases|Myopathy|_centronuclear|_2": 12,
    "BIN1-related_disorder|Myopathy|_centronuclear|_2": 4,
    "not_specified|not_provided|Myopathy|_centronuclear|_2": 6,
    "Myopathy|_centronuclear|_2|not_specified|not_provided": 5,
    "not_specified|Myopathy|_centronuclear|_2|not_provided": 6,
    "Myopathy|_centronuclear|_2|not_specified": 7,
    "not_specified|Myopathy|_centronuclear|_2": 5,
    "Inborn_genetic_diseases|Myopathy|_centronuclear|_2|not_provided": 1,
    "Myopathy|_centronuclear|_2|Inborn_genetic_diseases": 13,
    "Myopathy|_centronuclear|_2|not_provided|Inborn_genetic_diseases": 1,
    "Myopathy|_centronuclear|_2|See_cases": 1,
    "not_provided|Myopathy|_centronuclear|_2|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Myopathy|_centronuclear|_2|not_provided": 1,
    "Myopathy|_centronuclear|_2|Inborn_genetic_diseases|not_provided": 3,
    "Myopathy|_centronuclear|_2|not_provided|BIN1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Myopathy|_centronuclear|_2": 2,
    "BIN1-related_disorder": 4,
    "Myopathy|_centronuclear|_2|not_provided|not_specified": 4,
    "not_specified|Myopathy|_centronuclear|_2|Inborn_genetic_diseases": 1,
    "not_provided|Myopathy|_centronuclear|_2|not_specified": 2,
    "Myopathy|_centronuclear|_2|BIN1-related_disorder|not_provided": 1,
    "BIN1-related_disorder|Myopathy|_centronuclear|_2|not_specified": 1,
    "not_provided|BIN1-related_disorder": 1,
    "Myopathy|_centronuclear|_2|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Myopathy|_centronuclear|_2": 1,
    "Xeroderma_pigmentosum_group_B|not_provided": 11,
    "Xeroderma_pigmentosum|not_provided": 30,
    "Xeroderma_pigmentosum_group_B": 19,
    "not_provided|Xeroderma_pigmentosum_group_B": 15,
    "ERCC3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum": 6,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_B|ERCC3-related_disorder": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_B": 2,
    "Xeroderma_pigmentosum_group_B|Xeroderma_pigmentosum|not_provided": 2,
    "Inborn_genetic_diseases|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B|not_provided": 1,
    "Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|ERCC3-related_disorder|Xeroderma_pigmentosum": 1,
    "ERCC3-related_disorder|not_specified|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_B": 1,
    "Xeroderma_pigmentosum_group_B|not_provided|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive|not_provided": 6,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum_group_B": 4,
    "Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive|not_provided|Xeroderma_pigmentosum": 1,
    "Trichothiodystrophy_2|_photosensitive|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ERCC3-related_disorder|Xeroderma_pigmentosum|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum": 100,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_B": 2,
    "not_provided|Xeroderma_pigmentosum": 35,
    "Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B": 3,
    "Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B|not_provided": 3,
    "not_provided|ERCC3-related_disorder|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive": 1,
    "not_provided|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_B|Inborn_genetic_diseases": 1,
    "Trichothiodystrophy_2|_photosensitive": 3,
    "Inborn_genetic_diseases|Ovarian_cancer": 3,
    "not_provided|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum": 1,
    "ERCC3-related_disorder|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "not_provided|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive": 2,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive": 1,
    "Xeroderma_pigmentosum_group_B|Xeroderma_pigmentosum|Trichothiodystrophy_2|_photosensitive|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive": 1,
    "not_provided|Ovarian_cancer": 5,
    "not_provided|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B|Xeroderma_pigmentosum": 1,
    "Ovarian_cancer|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum_group_B": 2,
    "Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive|Inborn_genetic_diseases|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum": 4,
    "not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive": 2,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_B|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum_group_B": 1,
    "Trichothiodystrophy_2|_photosensitive|not_provided|ERCC3-related_disorder": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|Trichothiodystrophy_2|_photosensitive|not_provided|Xeroderma_pigmentosum_group_B": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive|not_provided": 1,
    "not_provided|not_specified|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B": 1,
    "not_provided|Xeroderma_pigmentosum|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B|ERCC3-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Xeroderma_pigmentosum_group_B|Trichothiodystrophy_2|_photosensitive": 1,
    "Xeroderma_pigmentosum_group_B|Inborn_genetic_diseases|not_provided": 1,
    "Xeroderma_pigmentosum|Trichothiodystrophy_2|_photosensitive|Xeroderma_pigmentosum_group_B|not_provided": 1,
    "ERCC3-related_disorder": 1,
    "MAP3K2-related_condition": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_provided": 8,
    "PROC-related_disorder": 8,
    "PROC-related_disorder|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 4,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 224,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_specified|not_provided": 1,
    "PROC-related_disorder|not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 4,
    "PROC-related_disorder|not_specified": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 11,
    "PROC-related_disorder|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|not_provided": 1,
    "Reduced_protein_C_activity|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_provided": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 12,
    "Reduced_protein_C_activity": 15,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|not_provided": 6,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thromboembolism|Deep_venous_thrombosis|not_provided": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|PROC-related_disorder|not_specified": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_specified": 4,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_provided": 4,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|not_provided|Hereditary_thrombophilia_due_to_congenital_protein_C_deficiency": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|PROC-related_disorder": 1,
    "Abnormal_thrombosis|Cerebral_palsy|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|PROC-related_disorder": 1,
    "Hereditary_angioedema_with_normal_C1Inh": 16,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|PROC-related_disorder": 8,
    "Reduced_protein_C_activity|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 5,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 2,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Reduced_protein_C_activity": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thromboembolism|Deep_venous_thrombosis": 1,
    "Inborn_genetic_diseases|not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "PROC-related_disorder|Thromboembolism|Deep_venous_thrombosis|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|not_provided": 1,
    "PROC-related_disorder|Reduced_protein_C_activity|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_specified": 1,
    "not_provided|PROC-related_disorder": 1,
    "not_provided|Reduced_protein_C_activity|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 3,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 7,
    "Thrombophilia_3_due_to_protein_C_deficiency|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Reduced_protein_C_activity": 1,
    "Deep_venous_thrombosis|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 2,
    "not_specified|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "Reduced_protein_C_activity|not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_provided|Reduced_protein_C_activity": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Reduced_protein_C_activity": 1,
    "Deep_venous_thrombosis": 4,
    "not_specified|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|not_provided|not_specified": 1,
    "not_provided|not_specified|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 1,
    "Reduced_protein_C_activity|Deep_venous_thrombosis|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "Thromboembolism|not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 4,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 1,
    "not_provided|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Hereditary_thrombophilia_due_to_congenital_protein_C_deficiency": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Deep_venous_thrombosis": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive|PROC-related_disorder|not_provided": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Reduced_protein_C_activity|PROC-related_disorder": 1,
    "Thrombophilia_3_due_to_protein_C_deficiency": 1,
    "Reduced_protein_C_activity|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_C_deficiency|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Reduced_protein_C_activity": 1,
    "Thrombophilia_due_to_protein_C_deficiency|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Hereditary_thrombophilia_due_to_congenital_protein_C_deficiency": 1,
    "MYO7B-related_disorder": 70,
    "not_provided|MYO7B-related_disorder": 9,
    "not_specified|MYO7B-related_disorder": 6,
    "MYO7B-related_disorder|not_provided": 2,
    "MYO7B-related_disorder|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W": 236,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W": 17,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|not_provided": 6,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|not_specified": 27,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|not_specified|not_provided": 1,
    "LIMS2-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|not_provided|LIMS2-related_disorder": 1,
    "LIMS2-related_disorder": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|not_specified": 1,
    "LIMS2-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W|LIMS2-related_disorder": 1,
    "not_provided|LIMS2-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2W": 1,
    "SAP130-related_disorder": 1,
    "CONGENITAL_DISORDER_OF_GLYCOSYLATION|_TYPE_IIcc": 8,
    "Hypogonadotropic_hypogonadism_15_with_anosmia": 2,
    "Hypogonadotropic_hypogonadism_15_with_or_without_anosmia|not_specified|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|HYPOGONADOTROPIC_HYPOGONADISM_15_WITH_OR_WITHOUT_ANOSMIA|_SUSCEPTIBILITY_TO|HS6ST1-related_disorder|not_provided": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided": 11,
    "HS6ST1-related_disorder": 8,
    "Hypogonadotropic_hypogonadism_15_with_or_without_anosmia": 3,
    "Hypogonadotropic_hypogonadism_15_with_anosmia|not_provided|not_specified|HS6ST1-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_15_with_anosmia|not_provided": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided|Hypogonadotropic_hypogonadism_15_with_or_without_anosmia": 1,
    "not_provided|HS6ST1-related_disorder": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_arthrogryposis|_and_structural_brain_anomalies": 33,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_arthrogryposis|_and_structural_brain_anomalies": 4,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_microcephaly|_arthrogryposis|_and_structural_brain_anomalies": 1,
    "Abnormal_cerebral_morphology|Neurodevelopmental_disorder_with_microcephaly|_arthrogryposis|_and_structural_brain_anomalies": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_arthrogryposis|_and_structural_brain_anomalies|not_provided": 1,
    "Primary_microcephaly|Seizure|Lissencephaly|Global_developmental_delay": 1,
    "not_provided|CCDC115-related_disorder": 2,
    "CCDC115-CDG": 5,
    "CCDC115-related_disorder|not_provided": 2,
    "Neutropenia|_severe_congenital|_8|_autosomal_dominant": 5,
    "CCDC115-CDG|not_provided": 1,
    "not_provided|CCDC115-CDG|Congenital_disorders_of_glycosylation_type_II": 1,
    "Congenital_disorders_of_glycosylation_type_II|CCDC115-CDG": 1,
    "not_specified|not_provided|Heterotaxy|_visceral|_2|_autosomal": 1,
    "Heterotaxy|_visceral|_2|_autosomal": 7,
    "Heterotaxy|_visceral|_2|_autosomal|not_specified": 1,
    "ARHGEF4-related_disorder": 13,
    "not_specified|ARHGEF4-related_disorder": 1,
    "ARHGEF4-related_disorder|not_provided": 2,
    "not_provided|ARHGEF4-related_disorder": 1,
    "Keratoconus_9": 5,
    "Leukodystrophy|_hypomyelinating|_25": 5,
    "Leukodystrophy|_hypomyelinating|_25|not_provided": 1,
    "not_provided|ACMSD-related_disorder": 1,
    "ACMSD-related_disorder": 2,
    "not_specified|not_provided|Warburg_micro_syndrome": 1,
    "Warburg_micro_syndrome_1|RAB3GAP1-related_disorder|not_specified": 1,
    "Martsolf_syndrome|Martsolf_syndrome_2": 1,
    "not_provided|RAB3GAP1-related_disorder": 7,
    "Warburg_micro_syndrome_1": 67,
    "RAB3GAP1-related_disorder": 8,
    "Cryptorchidism|Cleft_palate|Developmental_cataract|Movement_disorder|Humeral_cortical_thickening|Cortical_thickening_of_humeral_diaphysis|Thoracolumbar_scoliosis|Hypertrichosis|Spasticity|Bilateral_microphthalmos|Low-set_ears|Absent_speech|Rigidity|Abnormal_corpus_callosum_morphology|Congenital_ptosis|Infantile_axial_hypotonia|Intellectual_disability|_severe|Cerebral_hypomyelination": 1,
    "Martsolf_syndrome_2|Warburg_micro_syndrome_1": 1,
    "RAB3GAP1-related_disorder|Warburg_micro_syndrome_1|not_provided": 2,
    "Warburg_micro_syndrome_1|not_provided": 15,
    "not_specified|not_provided|Warburg_micro_syndrome_1": 4,
    "Warburg_micro_syndrome": 12,
    "not_specified|Warburg_micro_syndrome_1|not_provided": 3,
    "not_provided|Warburg_micro_syndrome_1": 10,
    "Inborn_genetic_diseases|RAB3GAP1-related_disorder|not_provided": 1,
    "not_provided|Warburg_micro_syndrome_1|Martsolf_syndrome_2": 2,
    "RAB3GAP1-related_disorder|not_provided": 6,
    "Martsolf_syndrome_2": 2,
    "not_specified|RAB3GAP1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Warburg_micro_syndrome_1": 1,
    "not_provided|not_specified|RAB3GAP1-related_disorder": 2,
    "Warburg_micro_syndrome_1|not_specified|RAB3GAP1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Warburg_micro_syndrome_1|Amenorrhea": 1,
    "Martsolf_syndrome_2|Warburg_micro_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Warburg_micro_syndrome_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Martsolf_syndrome_2|Warburg_micro_syndrome_1": 1,
    "RAB3GAP1-related_disorder|not_provided|Warburg_micro_syndrome_1": 1,
    "RAB3GAP1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Warburg_micro_syndrome_1": 1,
    "Warburg_micro_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Martsolf_syndrome_2|Warburg_micro_syndrome_1|not_provided": 2,
    "not_specified|RAB3GAP1-related_disorder|Warburg_micro_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Warburg_micro_syndrome_1|not_provided": 1,
    "Warburg_micro_syndrome_1|Martsolf_syndrome_2|not_specified|not_provided|Warburg_micro_syndrome": 1,
    "RAB3GAP1-related_disorder|not_specified|not_provided|Warburg_micro_syndrome_1": 1,
    "Martsolf_syndrome_2|not_provided": 1,
    "not_specified|not_provided|RAB3GAP1-related_disorder": 1,
    "not_provided|not_specified|Warburg_micro_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Martsolf_syndrome_2|Warburg_micro_syndrome_1": 1,
    "Warburg_micro_syndrome|not_provided": 3,
    "not_provided|Warburg_micro_syndrome": 1,
    "Congenital_lactase_deficiency|Lactose_intolerance": 12,
    "not_provided|Congenital_lactase_deficiency|Lactose_intolerance": 25,
    "Congenital_lactase_deficiency": 26,
    "not_provided|Congenital_lactase_deficiency|LCT-related_disorder|Lactose_intolerance": 2,
    "Congenital_lactase_deficiency|not_provided": 31,
    "Inborn_genetic_diseases|Congenital_lactase_deficiency|Lactose_intolerance": 2,
    "not_specified|not_provided|Congenital_lactase_deficiency|Lactose_intolerance": 5,
    "not_provided|LCT-related_disorder": 6,
    "LCT-related_disorder": 7,
    "LCT-related_disorder|not_provided": 4,
    "not_provided|Congenital_lactase_deficiency": 5,
    "Congenital_lactase_deficiency|not_provided|LCT-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_lactase_deficiency|Lactose_intolerance": 2,
    "not_provided|Congenital_lactase_deficiency|Lactose_intolerance|LCT-related_disorder": 6,
    "Congenital_lactase_deficiency|not_provided|Lactose_intolerance|LCT-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_lactase_deficiency": 1,
    "not_provided|Congenital_lactase_deficiency|LCT-related_disorder|Inborn_genetic_diseases|Lactose_intolerance": 1,
    "not_provided|Congenital_lactase_deficiency|LCT-related_disorder|Lactose_intolerance|not_specified": 1,
    "LCT-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Congenital_lactase_deficiency|Inborn_genetic_diseases": 1,
    "LCT-related_disorder|Congenital_lactase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Lactose_intolerance|not_provided|Congenital_lactase_deficiency": 1,
    "Congenital_lactase_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Congenital_lactase_deficiency": 1,
    "not_provided|not_specified|Congenital_lactase_deficiency|Lactose_intolerance": 1,
    "not_provided|Congenital_lactase_deficiency|Inborn_genetic_diseases|Lactose_intolerance": 1,
    "Congenital_lactase_deficiency|Lactose_intolerance|not_provided|LCT-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_lactase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|LACTASE_PERSISTENCE": 1,
    "MCM6-related_disorder": 10,
    "LACTASE_PERSISTENCE": 6,
    "Nonpersistence_of_intestinal_lactase": 4,
    "Nonpersistence_of_intestinal_lactase|not_provided": 1,
    "Nonpersistence_of_intestinal_lactase|not_specified": 1,
    "MCM6-related_disorder|not_specified": 1,
    "Lactose_intolerance": 1,
    "MCM6-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity": 2,
    "Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity": 13,
    "Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity|not_provided": 3,
    "not_provided|DARS1-related_disorder": 4,
    "DARS1-related_disorder|not_provided|not_specified": 1,
    "DARS1-related_disorder|not_provided": 5,
    "DARS1-related_disorder": 2,
    "Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity|Inborn_genetic_diseases": 1,
    "Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity|DARS1-related_disorder|not_provided": 1,
    "Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Hypomyelination_with_brain_stem_and_spinal_cord_involvement_and_leg_spasticity": 1,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 130,
    "WHIM_syndrome_1": 22,
    "WHIM_syndrome_1|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 2,
    "WHIM_syndrome_1|not_provided": 1,
    "WHIM_syndrome_1|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|not_provided": 1,
    "not_provided|not_specified|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 1,
    "WHIM_syndrome_1|not_provided|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 1,
    "Inborn_genetic_diseases|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 2,
    "CXCR4-related_disorder|Inborn_genetic_diseases": 1,
    "WHIM_syndrome_1|Inherited_Immunodeficiency_Diseases": 1,
    "not_provided|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 8,
    "CXCR4-related_disorder|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 3,
    "CXCR4-related_disorder|not_specified|not_provided|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 1,
    "not_specified|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 2,
    "CXCR4-related_disorder|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|WHIM_syndrome_1": 1,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|CXCR4-related_disorder": 1,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|Inborn_genetic_diseases": 3,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|not_provided": 3,
    "not_provided|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|Inborn_genetic_diseases": 1,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|not_provided|Inborn_genetic_diseases": 1,
    "CXCR4-related_disorder": 5,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|not_provided|not_specified": 1,
    "not_provided|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|WHIM_syndrome_1": 1,
    "Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|not_specified|not_provided": 1,
    "not_specified|not_provided|WHIM_syndrome_1|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis": 1,
    "not_provided|Warts|_hypogammaglobulinemia|_infections|_and_myelokathexis|not_specified|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_classic_type": 52,
    "Inherited_susceptibility_to_asthma|Intellectual_disability|_autosomal_recessive_51": 1,
    "Pulmonary_arterial_hypertension|not_provided": 2,
    "Intellectual_disability|_autosomal_recessive_51": 4,
    "Inherited_susceptibility_to_asthma|HNMT-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_51|not_provided": 1,
    "HNMT-related_disorder|not_provided": 1,
    "not_specified|Inherited_susceptibility_to_asthma|Intellectual_disability|_autosomal_recessive_51|not_provided": 1,
    "HNMT-related_disorder": 2,
    "LRP1B-related_disorder": 92,
    "not_provided|LRP1B-related_disorder|not_specified": 3,
    "not_provided|LRP1B-related_disorder": 12,
    "LRP1B-related_disorder|not_provided": 18,
    "LRP1B-associated_developmental_disorder": 1,
    "Malignant_neoplastic_disease": 3,
    "not_specified|LRP1B-related_disorder": 1,
    "LRP1B-related_disorder|not_specified": 1,
    "not_specified|LRP1B-related_disorder|not_provided": 2,
    "KYNU-related_disorder": 5,
    "not_provided|KYNU-related_disorder": 1,
    "Congenital_NAD_deficiency_disorder|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 5,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2|not_provided": 1,
    "Catel-Manzke_syndrome": 15,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 4,
    "not_specified|not_provided|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 1,
    "not_provided|Congenital_NAD_deficiency_disorder|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 2,
    "Congenital_NAD_deficiency_disorder|not_provided": 1,
    "not_provided|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 1,
    "Hydroxykynureninuria": 2,
    "Hydroxykynureninuria|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 2,
    "Hydroxykynureninuria|not_provided|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 1,
    "KYNU-related_disorder|not_provided": 1,
    "not_specified|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_2": 1,
    "Catel-Manzke_syndrome|not_provided|Congenital_NAD_deficiency_disorder": 1,
    "Mowat-Wilson_syndrome": 890,
    "Mowat-Wilson_syndrome|not_provided": 57,
    "not_provided|Mowat-Wilson_syndrome": 64,
    "not_provided|Mowat-Wilson_syndrome|Inborn_genetic_diseases": 6,
    "not_specified|Mowat-Wilson_syndrome": 23,
    "Inborn_genetic_diseases|Mowat-Wilson_syndrome": 18,
    "ZEB2-related_disorder|Inborn_genetic_diseases|not_specified|Mowat-Wilson_syndrome": 2,
    "Mowat-Wilson_syndrome|Inborn_genetic_diseases": 24,
    "Mowat-Wilson_syndrome|not_specified|Inborn_genetic_diseases": 3,
    "Mowat-Wilson_syndrome|not_specified": 20,
    "Inborn_genetic_diseases|not_provided|not_specified|Mowat-Wilson_syndrome": 2,
    "not_specified|Mowat-Wilson_syndrome|Inborn_genetic_diseases": 3,
    "Lennox-Gastaut_syndrome|Mowat-Wilson_syndrome": 1,
    "Smith-Magenis_Syndrome-like": 5,
    "not_specified|Mowat-Wilson_syndrome|not_provided": 2,
    "ZEB2-related_disorder|Mowat-Wilson_syndrome|not_specified": 1,
    "Intellectual_disability|not_provided|Inborn_genetic_diseases|Mowat-Wilson_syndrome": 1,
    "ZEB2-related_disorder|Mowat-Wilson_syndrome": 6,
    "Inborn_genetic_diseases|not_specified|not_provided|Mowat-Wilson_syndrome": 9,
    "Mowat-Wilson_syndrome|ZEB2-related_disorder|Inborn_genetic_diseases": 1,
    "Mowat-Wilson_syndrome|ZEB2-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Mowat-Wilson_syndrome|ZEB2-related_disorder": 3,
    "Mowat-Wilson_syndrome|not_provided|not_specified": 3,
    "not_provided|Mowat-Wilson_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "ZEB2-related_disorder": 14,
    "Inborn_genetic_diseases|not_provided|Mowat-Wilson_syndrome|See_cases|Intellectual_disability": 1,
    "ZEB2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Mowat-Wilson_syndrome": 3,
    "Mowat-Wilson_syndrome|not_provided|Inborn_genetic_diseases": 6,
    "not_specified|not_provided|Mowat-Wilson_syndrome": 3,
    "Inborn_genetic_diseases|Mowat-Wilson_syndrome|not_specified": 5,
    "Mowat-Wilson_syndrome|ZEB2-related_disorder|not_provided": 1,
    "Mowat-Wilson_syndrome|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Mowat-Wilson_syndrome": 6,
    "Mowat-Wilson_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|ZEB2-related_disorder|Mowat-Wilson_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Mowat-Wilson_syndrome|not_provided": 1,
    "ZEB2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Mowat-Wilson_syndrome": 4,
    "Inborn_genetic_diseases|ZEB2-related_disorder|not_specified|not_provided|Mowat-Wilson_syndrome": 6,
    "Mowat-Wilson_syndrome|Inborn_genetic_diseases|not_specified": 3,
    "Mowat-Wilson_syndrome|not_specified|ZEB2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ZEB2-related_disorder|not_specified|Mowat-Wilson_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|Mowat-Wilson_syndrome": 3,
    "not_provided|not_specified|Mowat-Wilson_syndrome": 2,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Mowat-Wilson_syndrome": 1,
    "not_specified|not_provided|Mowat-Wilson_syndrome|Inborn_genetic_diseases": 1,
    "Megacolon": 5,
    "not_specified|ZEB2-related_disorder|not_provided|Mowat-Wilson_syndrome": 1,
    "not_specified|ZEB2-related_disorder|Mowat-Wilson_syndrome": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Mowat-Wilson_syndrome|ZEB2-related_disorder": 1,
    "Inborn_genetic_diseases|Mowat-Wilson_syndrome|not_provided": 2,
    "not_provided|Mowat-Wilson_syndrome|Cleft_lip/palate": 1,
    "Abnormality_of_the_nervous_system|Mowat-Wilson_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Mowat-Wilson_syndrome": 1,
    "not_provided|Mowat-Wilson_syndrome|ZEB2-related_disorder|Inborn_genetic_diseases": 1,
    "Hirschsprung_disease-intellectual_disability_syndrome|_late_infantile|Mowat-Wilson_syndrome": 1,
    "ZEB2-related_disorder|Inborn_genetic_diseases|Mowat-Wilson_syndrome": 1,
    "ZEB2-related_disorder|Mowat-Wilson_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Meier-Gorlin_syndrome_2": 8,
    "not_provided|Meier-Gorlin_syndrome_2": 3,
    "not_provided|ORC4-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|ORC4-related_disorder": 2,
    "Meier-Gorlin_syndrome_2|not_provided": 2,
    "not_specified|ORC4-related_disorder": 1,
    "Meier-Gorlin_syndrome_2|not_specified|not_provided": 2,
    "HP:0003549": 3,
    "Meier-Gorlin_syndrome_2|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|ORC4-related_disorder": 1,
    "Intellectual_Disability|_Dominant|not_specified|not_provided": 1,
    "Intellectual_Disability|_Dominant": 8,
    "Intellectual_disability|_autosomal_dominant_1": 918,
    "not_provided|Intellectual_disability|_autosomal_dominant_1": 97,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 4,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|not_specified": 3,
    "Intellectual_disability|_autosomal_dominant_1|not_provided": 77,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_1": 32,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases": 5,
    "Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases": 27,
    "not_specified|Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_1|MBD5-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant|Intellectual_disability|_autosomal_dominant_1": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_1": 30,
    "not_specified|MBD5-related_disorder|Intellectual_disability|_autosomal_dominant_1": 1,
    "Intellectual_disability|_autosomal_dominant_1|Autism_spectrum_disorder": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_1|not_provided": 3,
    "MBD5-related_disorder|MBD5_associated_neurodevelopmental_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "Intellectual_disability|_autosomal_dominant_1|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MBD5-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "Intellectual_disability|_autosomal_dominant_1|not_specified": 15,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_1": 10,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases|not_specified": 2,
    "MBD5-related_disorder|Intellectual_disability|_autosomal_dominant_1": 3,
    "Intellectual_disability|_autosomal_dominant_1|Microcephaly|not_provided": 1,
    "developmental_delay_with_intractable_seizures|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_dominant_1": 3,
    "MBD5-related_disorder": 14,
    "Intellectual_disability|_autosomal_dominant_1|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_1|not_specified": 3,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases|MBD5-related_disorder|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases|Chromosome_2q23.1_deletion_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 9,
    "Intellectual_Disability|_Dominant|Intellectual_disability|_autosomal_dominant_1": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_1": 4,
    "Autism_spectrum_disorder|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "MBD5-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_1": 2,
    "MBD5-related_disorder|Intellectual_Disability|_Dominant|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_1|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases|not_provided": 7,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_1|not_provided": 4,
    "Inborn_genetic_diseases|Intellectual_disability|Intellectual_disability|_autosomal_dominant_1": 1,
    "Intellectual_disability|_autosomal_dominant_1|not_provided|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|See_cases": 1,
    "MBD5-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_1": 2,
    "not_specified|Intellectual_disability|_autosomal_dominant_1|See_cases|not_provided": 1,
    "MBD5_associated_neurodevelopmental_disorder|not_provided": 1,
    "Inborn_genetic_diseases|MBD5-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_1": 2,
    "Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_1|not_provided|Inborn_genetic_diseases": 4,
    "MBD5-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_dominant_1": 3,
    "MBD5-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 2,
    "Inborn_genetic_diseases|MBD5-related_disorder|Intellectual_disability|_autosomal_dominant_1": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|Cleft_palate": 1,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_1": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|Intellectual_disability|_autosomal_dominant_1": 1,
    "MBD5-related_disorder|Intellectual_disability|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_1|MBD5-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_1|not_provided|Inborn_genetic_diseases|MBD5-related_disorder": 1,
    "not_provided|MBD5-related_disorder|Intellectual_disability|_autosomal_dominant_1": 2,
    "Seizure|not_provided|not_specified|Intellectual_disability|_autosomal_dominant_1": 1,
    "MBD5-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_1|Inborn_genetic_diseases": 1,
    "MBD5-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_1|Bilateral_tonic-clonic_seizure": 1,
    "Intellectual_disability|_autosomal_dominant_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "MBD5-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "MBD5-related_disorder|MBD5_associated_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|not_specified|Intellectual_disability|_autosomal_dominant_1|Intellectual_disability": 1,
    "Intellectual_Disability|_Dominant|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "Developmental_and_epileptic_encephalopathy|_31A": 569,
    "Intellectual_disability|_autosomal_dominant_1|MBD5-related_disorder": 2,
    "not_specified|Intellectual_disability|_autosomal_dominant_1|MBD5_associated_neurodevelopmental_disorder": 1,
    "not_provided|See_cases|Intellectual_disability|_autosomal_dominant_1": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_1": 1,
    "Intellectual_disability|_autosomal_dominant_1|not_specified|not_provided|MBD5-related_disorder": 1,
    "Seizure|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_1": 1,
    "Autistic_behavior": 13,
    "not_provided|MBD5-related_disorder": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_2": 28,
    "KIF5C-related_disorder": 18,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_2": 3,
    "Complex_cortical_dysplasia_with_other_brain_malformations_2|not_provided": 5,
    "Complex_cortical_dysplasia_with_other_brain_malformations_2|Cortical_dysplasia": 1,
    "not_provided|KIF5C-related_disorder": 6,
    "not_specified|Developmental_disorder": 1,
    "Jaw-winking_syndrome": 3,
    "KIF5C-related_disorder|not_provided|not_specified": 2,
    "Craniosynostosis_syndrome|Complex_cortical_dysplasia_with_other_brain_malformations_2|not_provided": 1,
    "not_provided|KIF5C-related_disorder|not_specified": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 7,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism": 10,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 3,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD": 269,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_specified": 2,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Homocystinuria-megaloblastic_anemia_cblD_type": 1,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 4,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Homocystinuria-megaloblastic_anemia_cblD_type|Cobalamin_C_disease|See_cases": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_provided": 6,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|MMADHC-related_disorder": 2,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Cobalamin_C_disease|not_provided": 1,
    "MMADHC-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD|MMADHC-related_disorder": 1,
    "not_specified|not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD|MMADHC-related_disorder": 1,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD|MMADHC-related_disorder": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism|MMADHC-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 3,
    "Homocystinuria-megaloblastic_anemia_cblD_type": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Inborn_genetic_diseases": 5,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_specified|not_provided": 2,
    "not_specified|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 1,
    "not_provided|Cobalamin_C_disease|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 1,
    "not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_provided": 2,
    "not_provided|not_specified|Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_specified|MMADHC-related_disorder": 1,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 1,
    "Isolated_methylmalonic_aciduria_cblD_type|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 3,
    "Inborn_genetic_diseases|Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Cobalamin_C_disease": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|Methylmalonic_aciduria_and_homocystinuria_type_cblD": 1,
    "MMADHC-related_disorder": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified": 1,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblD|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_provided": 1,
    "Nemaline_myopathy_2": 8420,
    "Nemaline_Myopathy|_Recessive": 6,
    "not_provided|Nemaline_myopathy_2": 357,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2": 153,
    "Nemaline_myopathy_2|Inborn_genetic_diseases": 114,
    "Nemaline_myopathy_2|not_provided|NEB-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Nemaline_myopathy_2": 78,
    "Inborn_genetic_diseases|Nemaline_myopathy_2": 150,
    "not_specified|not_provided|Nemaline_myopathy_2": 60,
    "Nemaline_myopathy_2|not_provided": 274,
    "NEB-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Nemaline_myopathy_2|Nemaline_myopathy": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|Nemaline_myopathy": 16,
    "Arthrogryposis_multiplex_congenita_6": 203,
    "not_specified|Nemaline_myopathy_2|not_provided": 18,
    "Nemaline_myopathy_2|not_specified|Arthrogryposis_multiplex_congenita_6|not_provided": 6,
    "Nemaline_myopathy|Nemaline_myopathy_2": 43,
    "not_provided|not_specified|Nemaline_myopathy_2": 21,
    "NEB-related_disorder|not_specified|not_provided|Nemaline_myopathy_2|Muscle_weakness|Congenital_muscular_dystrophy": 1,
    "NEB-related_disorder|Inborn_genetic_diseases|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided": 3,
    "Nemaline_myopathy_2|Nemaline_myopathy": 44,
    "Nemaline_myopathy_2|not_provided|Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6": 1,
    "not_specified|Inborn_genetic_diseases|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 101,
    "NEB-related_disorder|Nemaline_myopathy_2|not_provided": 9,
    "not_provided|Nemaline_myopathy_2|Inborn_genetic_diseases": 37,
    "not_provided|Nemaline_myopathy_2|not_specified|Arthrogryposis_multiplex_congenita_6": 3,
    "NEB-related_disorder|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided": 1,
    "not_provided|not_specified|Nemaline_myopathy_2|Inborn_genetic_diseases": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided": 38,
    "not_provided|Inborn_genetic_diseases|Nemaline_myopathy_2": 43,
    "Nemaline_myopathy_2|not_specified": 87,
    "Nemaline_myopathy_2|not_provided|not_specified": 10,
    "Nemaline_myopathy_2|Nemaline_myopathy|not_provided|NEB-related_disorder|Arthrogryposis_multiplex_congenita_6": 1,
    "Nemaline_myopathy_2|Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6": 11,
    "Nemaline_myopathy_2|Nemaline_myopathy|not_provided|Arthrogryposis_multiplex_congenita_6": 2,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|not_provided": 38,
    "not_provided|Nemaline_myopathy|Nemaline_myopathy_2": 3,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy|Nemaline_myopathy_2": 9,
    "NEB-related_disorder|Inborn_genetic_diseases|not_provided|Nemaline_myopathy_2": 5,
    "Inborn_genetic_diseases|not_specified|not_provided|Nemaline_myopathy_2": 10,
    "Nemaline_myopathy_2|NEB-related_disorder": 31,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy|not_provided": 7,
    "Nemaline_myopathy_2|not_provided|Arthrogryposis_multiplex_congenita_6": 4,
    "Nemaline_myopathy_2|Inborn_genetic_diseases|not_provided": 45,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|NEB-related_disorder": 2,
    "Nemaline_myopathy_2|not_provided|not_specified|Arthrogryposis_multiplex_congenita_6": 6,
    "not_specified|Nemaline_myopathy_2": 72,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy|Nemaline_myopathy_2|not_provided": 2,
    "Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy_2": 5,
    "Nemaline_myopathy_2|NEB-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|Nemaline_myopathy|not_provided": 8,
    "Nemaline_myopathy|not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|not_specified|not_provided": 6,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided": 10,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided|Nemaline_myopathy": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|Nemaline_myopathy|not_provided|Abnormality_of_the_neck|Low-set_ears|Dysphagia": 1,
    "Nemaline_myopathy_2|not_specified|not_provided": 15,
    "Nemaline_myopathy|not_provided": 7,
    "Nemaline_myopathy_2|NEB-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Nemaline_myopathy_2|not_specified": 25,
    "not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 3,
    "Nemaline_myopathy_2|not_specified|not_provided|Arthrogryposis_multiplex_congenita_6": 4,
    "NEB-related_disorder": 23,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Abnormality_of_the_musculature": 1,
    "not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2": 7,
    "Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6": 6,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 17,
    "NEB-related_disorder|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|NEB-related_disorder": 1,
    "Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy_2": 1,
    "Arthrogryposis_multiplex_congenita_6|See_cases|Nemaline_myopathy_2|Nemaline_myopathy|not_provided": 1,
    "Nemaline_myopathy|not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2": 2,
    "Nemaline_myopathy_2|NEB-related_disorder|not_provided": 7,
    "not_specified|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 2,
    "Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided": 2,
    "not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|NEB-related_disorder|not_provided": 2,
    "Nebulin-related_early-onset_distal_myopathy|not_provided|Nemaline_myopathy_2": 1,
    "See_cases|Nemaline_myopathy_2": 1,
    "NEB-related_disorder|Nemaline_myopathy|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided|Muscular_dystrophy|Progressive_proximal_muscle_weakness|Limb_pain": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|NEB-related_disorder": 1,
    "not_provided|Nemaline_myopathy_2|Nemaline_myopathy": 4,
    "Nemaline_myopathy_2|Nemaline_myopathy|not_provided": 3,
    "not_provided|NEB-related_disorder|Inborn_genetic_diseases|Nemaline_myopathy_2": 1,
    "NEB-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Nemaline_myopathy_2": 3,
    "NEB-related_disorder|not_provided|Nemaline_myopathy_2": 13,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy|not_specified|Nemaline_myopathy_2|not_provided": 2,
    "NEB-related_disorder|Nemaline_myopathy_2|not_specified": 3,
    "Nemaline_myopathy_2|not_provided|Inborn_genetic_diseases": 30,
    "not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 8,
    "not_provided|NEB-related_disorder|Nemaline_myopathy_2": 6,
    "Inborn_genetic_diseases|not_provided|Nemaline_myopathy|Nemaline_myopathy_2": 1,
    "NEB-related_disorder|Inborn_genetic_diseases|Nemaline_myopathy_2|not_provided": 3,
    "NEB-related_disorder|not_specified|not_provided|Nemaline_myopathy_2": 5,
    "See_cases|Arthrogryposis_multiplex_congenita_6": 1,
    "not_provided|Nemaline_myopathy_2|Inborn_genetic_diseases|not_specified": 2,
    "NEB-related_disorder|not_specified|Nemaline_myopathy_2": 1,
    "NEB-related_disorder|Nemaline_myopathy_2": 28,
    "Nemaline_myopathy|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 10,
    "not_provided|not_specified|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 4,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|Congenital_structural_myopathy": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy": 3,
    "Arthrogryposis_multiplex_congenita_6|not_provided": 4,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|Inborn_genetic_diseases|not_provided": 3,
    "Distal_myopathy|Nemaline_myopathy_2|not_provided|Inborn_genetic_diseases": 1,
    "Nemaline_myopathy|not_provided|Inborn_genetic_diseases|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy_2|NEB-related_disorder|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|Nemaline_myopathy_2": 4,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided|Inborn_genetic_diseases": 5,
    "Nemaline_myopathy_2|not_provided|NEB-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Nemaline_myopathy": 2,
    "Nemaline_myopathy_2|Peripheral_neuropathy|Inborn_genetic_diseases|not_specified|not_provided|Actin_accumulation_myopathy": 1,
    "Congenital_myopathy|Nemaline_myopathy_2": 1,
    "Nemaline_Myopathy|_Recessive|Nemaline_myopathy_2|not_provided|not_specified": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|NEB-related_disorder|Nemaline_myopathy|not_provided": 1,
    "Nemaline_myopathy|Non-immune_hydrops_fetalis|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 1,
    "Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2": 2,
    "not_provided|Limb-girdle_muscular_dystrophy|Nemaline_myopathy_2": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|NEB-related_disorder|not_provided": 1,
    "not_specified|Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy_2": 3,
    "Nemaline_myopathy_2|not_provided|Nemaline_myopathy|Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita_6": 1,
    "Nemaline_myopathy_2|not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 3,
    "not_specified|Nemaline_myopathy_2|Nemaline_Myopathy|_Recessive": 2,
    "not_specified|Nemaline_Myopathy|_Recessive": 1,
    "not_specified|not_provided|Nemaline_Myopathy|_Recessive": 1,
    "not_provided|not_specified|Nemaline_myopathy": 1,
    "not_specified|Nemaline_myopathy_2|Inborn_genetic_diseases": 5,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy|not_specified|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Inborn_genetic_diseases|not_provided": 7,
    "not_specified|NEB-related_disorder|not_provided|Inborn_genetic_diseases|Nemaline_myopathy_2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Nemaline_myopathy_2|Limb_pain|Muscular_dystrophy|Progressive_proximal_muscle_weakness": 1,
    "Nemaline_myopathy_2|Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita_6": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Nemaline_myopathy_2": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|NEB-related_disorder|Inborn_genetic_diseases|Nemaline_myopathy|not_provided": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Inborn_genetic_diseases": 3,
    "Nemaline_myopathy_2|Inborn_genetic_diseases|not_specified": 2,
    "Nemaline_Myopathy|_Recessive|Nemaline_myopathy_2": 2,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|NEB-related_disorder|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 2,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_specified|not_provided": 2,
    "NEB-related_disorder|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2": 2,
    "Nemaline_myopathy|Nemaline_myopathy_2|not_specified": 1,
    "Nemaline_myopathy_2|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2": 4,
    "Inborn_genetic_diseases|NEB-related_disorder|not_provided|Nemaline_myopathy_2": 1,
    "not_specified|NEB-related_disorder|not_provided|Nemaline_myopathy_2": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy|not_specified|Limb-girdle_muscular_dystrophy|Nemaline_myopathy_2|NEB-related_disorder|not_provided": 1,
    "not_specified|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided": 1,
    "Nemaline_myopathy_2|not_provided|Arthrogryposis_multiplex_congenita_6|not_specified": 1,
    "not_specified|Nemaline_myopathy_2|not_provided|Arthrogryposis_multiplex_congenita_6": 1,
    "NEB-related_disorder|Nemaline_myopathy_2|not_specified|Inborn_genetic_diseases": 1,
    "Nemaline_myopathy|not_provided|Nemaline_myopathy_2": 3,
    "Inborn_genetic_diseases|not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|NEB-related_disorder|not_provided": 1,
    "NEB-related_disorder|Nemaline_myopathy_2|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Nemaline_myopathy_2|not_provided": 1,
    "Nemaline_Myopathy|_Recessive|not_provided|Nemaline_myopathy_2|not_specified": 1,
    "Nemaline_myopathy|Nemaline_myopathy_2|not_provided": 1,
    "Nemaline_myopathy_2|Distal_myopathy|not_provided": 1,
    "not_provided|NEB-related_disorder|not_specified|Nemaline_myopathy_2": 2,
    "Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy_2|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Nemaline_myopathy_2|not_provided": 3,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|Congenital_structural_myopathy": 1,
    "not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_specified": 1,
    "not_provided|Peripheral_neuropathy|not_specified": 2,
    "NEB-related_disorder|not_specified": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided|NEB-related_disorder": 1,
    "Nemaline_myopathy_2|NEB-related_disorder|not_provided|Arthrogryposis_multiplex_congenita_6": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_provided|not_specified": 2,
    "not_specified|NEB-related_disorder|Nemaline_myopathy_2": 3,
    "Nemaline_myopathy_2|Nemaline_myopathy|Congenital_myopathy|Arthrogryposis_multiplex_congenita_6": 1,
    "Nemaline_myopathy_2|not_provided|Arthrogryposis_multiplex_congenita_6|NEB-related_disorder": 1,
    "not_provided|Nemaline_myopathy_2|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_specified": 3,
    "Nemaline_myopathy|Nemaline_myopathy_2|not_provided|Arthrogryposis_multiplex_congenita_6": 1,
    "not_provided|Nemaline_myopathy_2|NEB-related_disorder": 3,
    "not_provided|Nemaline_myopathy|not_specified|Nemaline_myopathy_2": 2,
    "Nemaline_myopathy_2|NEB-related_disorder|not_provided|Nemaline_myopathy": 1,
    "NEB-related_disorder|not_specified|Nemaline_myopathy_2|not_provided": 1,
    "NEB-related_disorder|Nemaline_myopathy_2|Inborn_genetic_diseases": 1,
    "NEB-related_disorder|Nemaline_myopathy|Nemaline_myopathy_2": 1,
    "not_specified|not_provided|Nemaline_myopathy_2|NEB-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|not_provided|not_specified": 1,
    "Nemaline_myopathy_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Nemaline_myopathy_2|Inborn_genetic_diseases|Congenital_structural_myopathy": 1,
    "NEB-related_disorder|Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided": 2,
    "not_specified|Nemaline_myopathy_2|NEB-related_disorder": 1,
    "not_provided|Nemaline_myopathy_2|Inborn_genetic_diseases|Nemaline_myopathy": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Nemaline_myopathy_2": 2,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy|not_provided|Nemaline_myopathy_2": 2,
    "not_provided|Arthrogryposis_multiplex_congenita_6|not_specified|Nemaline_myopathy_2": 1,
    "not_provided|Nemaline_myopathy_2|Nemaline_myopathy|Arthrogryposis_multiplex_congenita_6": 1,
    "not_specified|not_provided|Nemaline_myopathy_2|NEB-related_disorder": 1,
    "NEB-related_disorder|Inborn_genetic_diseases|not_provided|Limb-girdle_muscular_dystrophy|Nemaline_myopathy_2": 1,
    "NEB-related_disorder|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Nemaline_myopathy_2": 1,
    "Congenital_muscular_dystrophy|Muscle_weakness|Nemaline_myopathy_2": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|not_specified|Nemaline_myopathy": 1,
    "not_specified|Nemaline_myopathy_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|Inborn_genetic_diseases": 1,
    "Nemaline_myopathy|Nemaline_myopathy_2|NEB-related_disorder": 1,
    "Inborn_genetic_diseases|NEB-related_disorder|Nemaline_myopathy_2|not_provided": 1,
    "not_provided|Nemaline_myopathy_2|NEB-related_disorder|See_cases": 1,
    "Inborn_genetic_diseases|NEB-related_disorder|Nemaline_myopathy_2": 1,
    "not_provided|not_specified|Nemaline_myopathy_2|NEB-related_disorder": 1,
    "Nemaline_myopathy_2|NEB-related_disorder|Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy": 1,
    "not_specified|not_provided|NEB-related_disorder|Nemaline_myopathy_2": 1,
    "not_specified|Inborn_genetic_diseases|Nemaline_myopathy_2|NEB-related_disorder|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_6|Nemaline_myopathy_2|NEB-related_disorder|not_provided": 1,
    "not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|Congenital_myopathy": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 1,
    "not_specified|not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 1,
    "Nemaline_myopathy_2|Inborn_genetic_diseases|not_provided|NEB-related_disorder": 1,
    "not_provided|Arthrogryposis_multiplex_congenita_6": 1,
    "NEB-related_disorder|Nemaline_Myopathy|_Recessive|not_provided|Nemaline_myopathy_2": 1,
    "Nebulin-related_early-onset_distal_myopathy|not_specified|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided|not_specified": 1,
    "NEB-related_disorder|not_provided|not_specified|Inborn_genetic_diseases|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_specified": 1,
    "not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|Actin_accumulation_myopathy": 1,
    "Arthrogryposis_multiplex_congenita_6|not_specified|not_provided|Nemaline_myopathy_2": 3,
    "not_specified|NEB-related_disorder|Nemaline_myopathy_2|not_provided": 1,
    "NEB-related_disorder|Nemaline_myopathy_2|not_provided|not_specified": 1,
    "Arthrogryposis_multiplex_congenita_6|Inborn_genetic_diseases|not_provided|Nemaline_myopathy_2": 1,
    "not_specified|Nemaline_myopathy_2|NEB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Nebulin-related_early-onset_distal_myopathy": 1,
    "Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy_2|not_specified": 1,
    "Nemaline_myopathy|Nemaline_myopathy_2|not_provided|See_cases": 1,
    "Nemaline_myopathy_2|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Nemaline_myopathy_2|NEB-related_disorder": 1,
    "Congenital_myopathy|Nemaline_myopathy|Nemaline_myopathy_2|not_provided": 1,
    "not_specified|Nemaline_myopathy|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy|not_specified|not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 1,
    "NEB-related_disorder|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_6|Inborn_genetic_diseases|Nemaline_myopathy": 1,
    "Nemaline_myopathy_2|NEB-related_disorder|Arthrogryposis_multiplex_congenita_6": 1,
    "not_specified|Nemaline_myopathy|not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6": 1,
    "not_specified|not_provided|Nemaline_myopathy|Nemaline_myopathy_2": 1,
    "Nemaline_myopathy_2|Nemaline_Myopathy|_Recessive|not_provided": 1,
    "Nemaline_myopathy|not_specified": 1,
    "Arthrogryposis_multiplex_congenita_6|not_provided|Nemaline_myopathy_2|Nemaline_myopathy": 1,
    "NEB-related_disorder|Nemaline_myopathy_2|not_specified|not_provided": 1,
    "Congenital_structural_myopathy|not_provided|Arthrogryposis_multiplex_congenita_6|not_specified|Nemaline_myopathy_2": 1,
    "not_provided|Nemaline_myopathy_2|Arthrogryposis_multiplex_congenita_6|NEB-related_disorder|Nemaline_myopathy": 1,
    "Episodic_ataxia_type_5|Juvenile_myoclonic_epilepsy": 55,
    "Episodic_ataxia_type_5|Juvenile_myoclonic_epilepsy|not_provided": 8,
    "Episodic_ataxia_type_5": 40,
    "Juvenile_myoclonic_epilepsy|Hereditary_episodic_ataxia": 9,
    "Episodic_ataxia_type_5|not_provided|Juvenile_myoclonic_epilepsy": 4,
    "not_provided|Episodic_ataxia_type_5|Juvenile_myoclonic_epilepsy": 6,
    "Hereditary_episodic_ataxia|Juvenile_myoclonic_epilepsy": 6,
    "Hereditary_episodic_ataxia|Juvenile_myoclonic_epilepsy|not_provided": 1,
    "not_provided|Juvenile_myoclonic_epilepsy|Hereditary_episodic_ataxia": 1,
    "Juvenile_myoclonic_epilepsy|not_specified|Episodic_ataxia_type_5": 1,
    "not_provided|Episodic_ataxia_type_5": 1,
    "Idiopathic_generalized_epilepsy|not_specified|not_provided": 3,
    "not_specified|Episodic_ataxia_type_5|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9": 1,
    "Epilepsy|_juvenile_myoclonic|_susceptibility_to|_6": 1,
    "CACNB4-related_disorder": 3,
    "CACNB4-related_disorder|not_specified|not_provided|Idiopathic_generalized_epilepsy|Juvenile_myoclonic_epilepsy|Episodic_ataxia_type_5": 1,
    "not_provided|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|Episodic_ataxia_type_5": 1,
    "not_specified|Idiopathic_generalized_epilepsy|Episodic_ataxia_type_5": 1,
    "not_specified|not_provided|Idiopathic_generalized_epilepsy|Juvenile_myoclonic_epilepsy|Episodic_ataxia_type_5": 1,
    "not_specified|Episodic_ataxia_type_5|Idiopathic_generalized_epilepsy|Juvenile_myoclonic_epilepsy|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|not_specified": 1,
    "Idiopathic_generalized_epilepsy|CACNB4-related_disorder|not_specified": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_9": 5,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9": 1,
    "CACNB4-related_disorder|not_specified|not_provided|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Idiopathic_generalized_epilepsy|Episodic_ataxia_type_5|Juvenile_myoclonic_epilepsy|not_provided": 1,
    "not_provided|Idiopathic_generalized_epilepsy|not_specified|CACNB4-related_disorder": 1,
    "not_specified|not_provided|Juvenile_myoclonic_epilepsy|Episodic_ataxia_type_5": 1,
    "not_provided|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|Episodic_ataxia_type_5|Juvenile_myoclonic_epilepsy": 1,
    "not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|not_provided": 1,
    "CACNB4-related_disorder|not_provided|Juvenile_myoclonic_epilepsy|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|Episodic_ataxia_type_5": 1,
    "Juvenile_myoclonic_epilepsy|Hereditary_episodic_ataxia|not_provided": 1,
    "Episodic_ataxia_type_5|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|Idiopathic_generalized_epilepsy": 1,
    "Episodic_ataxia_type_5|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|not_specified|CACNB4-related_disorder|Idiopathic_generalized_epilepsy": 1,
    "CACNB4-related_disorder|not_provided": 1,
    "CACNB4-related_disorder|not_provided|not_specified": 1,
    "not_provided|Idiopathic_generalized_epilepsy|CACNB4-related_disorder|not_specified": 1,
    "CACNB4-related_disorder|Episodic_ataxia_type_5|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|not_specified|not_provided|Juvenile_myoclonic_epilepsy|Idiopathic_generalized_epilepsy": 1,
    "Idiopathic_generalized_epilepsy|Episodic_ataxia_type_5": 1,
    "Idiopathic_generalized_epilepsy|CACNB4-related_disorder|not_specified|not_provided": 1,
    "not_specified|Episodic_ataxia_type_5|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Idiopathic_generalized_epilepsy|Juvenile_myoclonic_epilepsy|not_provided|Episodic_ataxia_type_5": 1,
    "CACNB4-related_disorder|not_specified|Episodic_ataxia_type_5|Epilepsy|_idiopathic_generalized|_susceptibility_to|_9|not_provided|Idiopathic_generalized_epilepsy|Juvenile_myoclonic_epilepsy": 1,
    "Juvenile_myoclonic_epilepsy|not_specified|not_provided|Episodic_ataxia_type_5": 1,
    "Crohn_disease": 1,
    "FMNL2-related_disorder": 3,
    "not_specified|FMNL2-related_disorder": 1,
    "Mycotic_Aneurysm|_Intracranial": 2,
    "not_provided|Parkinson_Disease|_Dominant/Recessive": 3,
    "Parkinson_Disease|_Dominant/Recessive": 54,
    "not_provided|Parkinson_disease|_late-onset": 3,
    "Intellectual_developmental_disorder_with_language_impairment_and_early-onset_DOPA-responsive_dystonia-parkinsonism": 46,
    "NR4A2-related_disorder": 4,
    "Parkinson_disease|_late-onset|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_language_impairment_and_early-onset_DOPA-responsive_dystonia-parkinsonism|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_language_impairment_and_early-onset_DOPA-responsive_dystonia-parkinsonism|not_provided": 1,
    "NR4A2-related_disorder|not_provided|Parkinson_disease|_late-onset": 1,
    "not_provided|Intellectual_developmental_disorder_with_language_impairment_and_early-onset_DOPA-responsive_dystonia-parkinsonism": 1,
    "not_provided|Intellectual_developmental_disorder_with_language_impairment_and_early-onset_DOPA-responsive_dystonia-parkinsonism|Neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "not_specified|NR4A2-related_disorder|not_provided": 1,
    "GPD2-related_disorder": 6,
    "not_provided|not_specified|Type_2_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|not_provided": 16,
    "not_provided|GPD2-related_disorder": 1,
    "Type_2_diabetes_mellitus": 159,
    "ACVR1C-related_disorder": 6,
    "ACVR1C-related_disorder|not_provided": 3,
    "Progressive_myositis_ossificans": 36,
    "not_provided|Progressive_myositis_ossificans": 13,
    "Progressive_myositis_ossificans|not_provided": 6,
    "not_provided|Progressive_myositis_ossificans|ACVR1-related_disorder": 2,
    "not_provided|ACVR1-related_disorder": 1,
    "not_provided|Congenital_heart_disease": 5,
    "ACVR1-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|Progressive_myositis_ossificans": 1,
    "not_provided|Progressive_myositis_ossificans|not_specified": 2,
    "Inborn_genetic_diseases|Epicanthus|Progressive_myositis_ossificans|not_provided|ACVR1-related_disorder": 1,
    "ACVR1-related_disorder|not_provided": 2,
    "Congenital_heart_disease|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Progressive_myositis_ossificans|ACVR1-related_disorder|Multiple_congenital_anomalies/dysmorphic_syndrome": 1,
    "Progressive_myositis_ossificans|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Progressive_myositis_ossificans": 1,
    "Autism_spectrum_disorder|not_specified": 9,
    "BAZ2B-related_disorder": 44,
    "BAZ2B-associated_neurodevelopmental_disorder": 1,
    "BAZ2B-related_disorder|not_provided": 2,
    "not_provided|BAZ2B-associated_neurodevelopmental_disorder": 1,
    "not_provided|BAZ2B-related_disorder": 2,
    "BAZ2B-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|BAZ2B-related_disorder": 1,
    "Inborn_genetic_diseases|BAZ2B-related_disorder": 6,
    "BAZ2B-related_Neurodevelopmental_disorder": 4,
    "not_provided|BAZ2B-related_disorder|Inborn_genetic_diseases": 1,
    "BAZ2B-related_disorder|See_cases": 1,
    "not_specified|Kidney_disorder": 2,
    "Amelogenesis_imperfecta_type_1H|not_specified|not_provided": 1,
    "Amelogenesis_imperfecta_type_1H": 10,
    "ITGB6-related_disorder": 4,
    "Amelogenesis_imperfecta_type_1H|not_provided": 2,
    "not_provided|ITGB6-related_disorder": 4,
    "not_provided|ITGB6-related_disorder|Inborn_genetic_diseases": 1,
    "Adolescent_alopeciam_dentogingival_abnormalitites_and_intellectual_disability": 1,
    "ITGB6-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autism_and_speech_delay": 2,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay": 49,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay|not_specified": 1,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|TBR1-related_disorder": 1,
    "TBR1-related_neurodevelopmental_disorder": 1,
    "TBR1-related_disorder": 9,
    "Moderate_global_developmental_delay|Autistic_behavior": 4,
    "Attention_deficit_hyperactivity_disorder|Moderate_global_developmental_delay|Autistic_behavior|Aggressive_behavior": 1,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay|Inborn_genetic_diseases": 4,
    "not_provided|Seizure": 12,
    "Severe_global_developmental_delay|Autistic_behavior": 2,
    "Moderate_global_developmental_delay|Autistic_behavior|Intellectual_disability": 1,
    "not_provided|Severe_global_developmental_delay|Autistic_behavior": 1,
    "Moderate_global_developmental_delay|Autistic_behavior|Marfanoid_habitus_and_intellectual_disability": 1,
    "Attention_deficit_hyperactivity_disorder|Autistic_behavior|Moderate_global_developmental_delay|Delayed_fine_motor_development": 1,
    "Limb_myoclonus|Severe_global_developmental_delay|Autistic_behavior|Aggressive_behavior": 1,
    "Moderate_global_developmental_delay|Atypical_behavior|Aplasia/Hypoplasia_of_the_corpus_callosum|Seizure|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_autism_and_speech_delay|TBR1-related_disorder": 1,
    "TBR1-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay|Neurodevelopmental_disorder": 1,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay|not_provided": 2,
    "Intellectual_disability|Moderate_global_developmental_delay|Autistic_behavior": 1,
    "Neurodevelopmental_disorder|Focal_cortical_dysplasia|Delayed_fine_motor_development|Severe_global_developmental_delay|Gait_ataxia|Seizure|Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies|Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_autism_and_speech_delay|Autistic_behavior|Intellectual_disability|Abnormal_brainstem_MRI_signal_intensity|Moderate_global_developmental_delay|Hypoplasia_of_the_frontal_lobes": 1,
    "TBR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Delayed_fine_motor_development|Severe_global_developmental_delay|Gait_disturbance|Seizure|Aggressive_behavior": 1,
    "Hypoplastic_hippocampus|Hypoplastic_anterior_commissure|Generalized_hypotonia|Cortical_dysplasia|Inflexible_adherence_to_routines|Severe_global_developmental_delay|EEG_abnormality|Gait_disturbance|Abnormal_facial_shape|Absent_speech": 1,
    "Intellectual_disability|Severe_global_developmental_delay|Autistic_behavior": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autism_and_speech_delay|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder_with_autism_and_speech_delay|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_autism_and_speech_delay|History_of_neurodevelopmental_disorder|not_provided": 1,
    "SLC4A10-related_disorder": 6,
    "Neurodevelopmental_disorder_with_hypotonia_and_characteristic_brain_abnormalities": 7,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia_and_characteristic_brain_abnormalities": 1,
    "SLC4A10-related_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia_and_characteristic_brain_abnormalities": 3,
    "not_specified|SLC4A10-related_disorder": 1,
    "SLC4A10-related_disorder|not_specified|not_provided": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 627,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 461,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_provided": 21,
    "Immunodeficiency_95": 4,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Inborn_genetic_diseases": 29,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified|not_provided": 1,
    "Basal_ganglia_calcification|_idiopathic|_childhood-onset|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|IFIH1-related_disorder": 1,
    "not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 26,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided": 33,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 10,
    "Aicardi-Goutieres_syndrome_7": 29,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Immunodeficiency_95": 2,
    "IFIH1-related_disorder|not_specified|not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Inborn_genetic_diseases": 11,
    "not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 30,
    "Immunodeficiency_95|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 5,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|not_provided": 2,
    "IFIH1-related_disorder|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Immunodeficiency_95": 2,
    "not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Immunodeficiency_95|IFIH1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency_95|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified|not_provided": 1,
    "not_provided|IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified": 1,
    "Susceptibility_to_severe_COVID-19|Immunodeficiency_95|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "IFIH1-related_disorder|not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 1,
    "Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|Singleton-Merten_syndrome_1": 1,
    "Inborn_genetic_diseases|not_specified|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Inborn_genetic_diseases|not_provided": 3,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_specified": 2,
    "not_provided|not_specified|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 2,
    "Inborn_genetic_diseases|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 12,
    "Inborn_genetic_diseases|IFIH1-related_disorder|not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "Immunodeficiency_95|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|IFIH1-related_interferonopathy|not_provided": 1,
    "not_specified|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_provided": 2,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|not_provided|IFIH1-related_disorder|Inborn_genetic_diseases": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Aicardi-Goutieres_syndrome_7": 4,
    "IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Inborn_genetic_diseases|not_provided|Incidental_Discovery": 1,
    "not_specified|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 5,
    "IFIH1-related_disorder|not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Inborn_genetic_diseases|IFIH1-related_disorder": 2,
    "IFIH1-related_disorder|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 15,
    "IFIH1-related_disorder|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Inborn_genetic_diseases": 3,
    "Singleton-Merten_syndrome_1|Immunodeficiency_95|Aicardi-Goutieres_syndrome_7|IFIH1-related_disorder|not_provided": 1,
    "IFIH1-related_disorder|Immunodeficiency_95|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|Hyperreflexia|Neonatal_hypotonia|Abnormal_upper_motor_neuron_morphology|Abnormal_basal_ganglia_morphology|Developmental_regression|Abnormal_cerebral_white_matter_morphology|Clonus": 1,
    "Aicardi-Goutieres_syndrome_7|IFIH1-related_disorder|Singleton-Merten_syndrome_1": 1,
    "Inborn_genetic_diseases|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_specified": 1,
    "Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|Singleton-Merten_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|See_cases": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|IFIH1-related_disorder|not_provided": 1,
    "IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 2,
    "not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95": 4,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|See_cases|not_specified|Immunodeficiency_95": 1,
    "IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_provided": 2,
    "IFIH1-related_type_1_interferonopathy|Immunodeficiency_95": 1,
    "not_specified|not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 1,
    "not_provided|IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified|Immunodeficiency_95": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|not_provided|IFIH1-related_type_1_interferonopathy|Multisystem_inflammatory_syndrome_in_children": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_provided|Vascular_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "Inborn_genetic_diseases|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided": 1,
    "Singleton-Merten_syndrome_1|Immunodeficiency_95|Aicardi-Goutieres_syndrome_7|not_provided|IFIH1-related_disorder|Inborn_genetic_diseases|IFIH1-related_immunodeficiency": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|See_cases|not_provided": 1,
    "not_specified|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|Basal_ganglia_calcification|_idiopathic|_childhood-onset": 1,
    "IFIH1-related_disorder": 4,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_provided|Immunodeficiency_95": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|Inborn_genetic_diseases": 2,
    "IFIH1-related_disorder|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided": 2,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Immunodeficiency_95|Inborn_genetic_diseases": 1,
    "Hereditary_predisposition_to_infections": 1,
    "not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Immunodeficiency_95|Susceptibility_to_severe_COVID-19|not_specified|Multisystem_inflammatory_syndrome_in_children": 1,
    "Singleton-Merten_syndrome_1|Immunodeficiency_95|Aicardi-Goutieres_syndrome_7": 4,
    "not_specified|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Inborn_genetic_diseases": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|not_specified": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|IFIH1-related_disorder": 3,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|not_specified": 2,
    "not_provided|Aicardi-Goutieres_syndrome_7|Spastic_diplegia": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|Immunodeficiency_95": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_7|not_provided|Singleton-Merten_syndrome_1": 1,
    "Singleton-Merten_syndrome_1": 2,
    "not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Inborn_genetic_diseases|IFIH1-related_disorder": 1,
    "Aicardi-Goutieres_syndrome_7|not_provided": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided|IFIH1-related_disorder": 2,
    "Immunodeficiency_95|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 2,
    "IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|Singleton-Merten_syndrome_1|not_specified|not_provided|IFIH1-related_immunodeficiency": 1,
    "IFIH1-related_disorder|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|Singleton-Merten_syndrome_1|not_specified|not_provided": 1,
    "IFIH1-related_type_1_interferonopathy|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 2,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95": 2,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|IFIH1-related_disorder": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|Immunodeficiency_95|Inborn_genetic_diseases": 1,
    "Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|See_cases": 1,
    "Aicardi_Goutieres_syndrome": 48,
    "not_specified|Intellectual_disability|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1": 1,
    "not_specified|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7|not_provided": 2,
    "IFIH1-related_disorder|Basal_ganglia_calcification|_idiopathic|_childhood-onset|not_provided|Singleton-Merten_syndrome_1|Aicardi-Goutieres_syndrome_7": 1,
    "Aicardi-Goutieres_syndrome_7|Singleton-Merten_syndrome_1|Immunodeficiency_95|not_provided": 1,
    "Singleton-Merten_syndrome_1|Immunodeficiency_95|Aicardi-Goutieres_syndrome_7|Inborn_genetic_diseases|not_specified": 1,
    "Aicardi-Goutieres_syndrome_7|Inborn_genetic_diseases|Singleton-Merten_syndrome_1": 1,
    "KCNH7-related_disorder": 10,
    "not_provided|KCNH7-related_disorder": 1,
    "SCN3A-related_disorder|not_provided|not_specified": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Developmental_and_epileptic_encephalopathy|_62": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_4": 6,
    "not_provided|SCN3A-related_disorder": 13,
    "SCN3A-related_disorder": 10,
    "Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4": 4,
    "SCN3A-related_disorder|not_provided": 10,
    "Developmental_and_epileptic_encephalopathy|_62": 22,
    "not_provided|Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4": 6,
    "Developmental_and_epileptic_encephalopathy|_62|not_provided": 8,
    "not_provided|Developmental_and_epileptic_encephalopathy|SCN3A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_62|Inborn_genetic_diseases": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|_62": 1,
    "Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|not_provided": 7,
    "Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|SCN3A-related_disorder|Inborn_genetic_diseases": 3,
    "Epilepsy|_familial_focal|_with_variable_foci_4": 10,
    "not_provided|Developmental_and_epileptic_encephalopathy|_62": 5,
    "Developmental_and_epileptic_encephalopathy|_62|Congenital_bilateral_perisylvian_syndrome|not_provided": 1,
    "SCN3A-related_disorder|not_specified|not_provided": 2,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|_62": 5,
    "not_provided|Inborn_genetic_diseases|SCN3A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_62|SCN3A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_4": 3,
    "Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|_62|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_focal|_SCN3A_related": 1,
    "SCN3A-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Epilepsy|_familial_focal|_with_variable_foci_4|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Developmental_delay|Polymicrogyria|Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|not_provided|Developmental_and_epileptic_encephalopathy|Epilepsy": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|_62|not_specified": 3,
    "not_provided|See_cases|Epilepsy|_familial_focal|_with_variable_foci_4": 1,
    "not_specified|not_provided|Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|_62": 2,
    "Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|SCN3A-related_neurodevelopmental_disorder": 2,
    "SCN3A-related_neurodevelopmental_sisorder|not_provided": 1,
    "SCN3A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SCN3A-related_disorder": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_7": 2,
    "Epilepsy|_familial_focal|_with_variable_foci_4|Developmental_and_epileptic_encephalopathy|_62|not_provided|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|not_specified": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|SCN3A-related_disorder|Seizure|not_provided": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4": 1,
    "SCN3A-related_neurodevelopmental_sisorder": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_4|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_62|atypical_cerebral_palsy|not_provided": 1,
    "not_specified|not_provided|SCN3A-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_62|Epilepsy|_familial_focal|_with_variable_foci_4|not_specified|SCN3A-related_disorder": 1,
    "not_provided|Epilepsy|_focal|_SCN3A_related": 1,
    "not_provided|Seizures|_benign_familial_infantile|_3|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant": 4,
    "Episodic_ataxia|_type_9|not_provided|Seizures|_benign_familial_infantile|_3|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant": 2,
    "Seizures|_benign_familial_infantile|_3|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant": 12,
    "Developmental_and_epileptic_encephalopathy|_11": 109,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 687,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 397,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 49,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 94,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 3,
    "not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 81,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|not_provided|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 5,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|not_provided": 4,
    "SCN2A-related_disorder|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 3,
    "SCN2A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder|not_provided": 1,
    "SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 2,
    "SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 5,
    "Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 39,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified": 24,
    "Non-syndromic_intellectual_disability": 5,
    "not_provided|Continuous_spikes_and_waves_during_sleep|Seizures|_benign_familial_infantile|_3|Non-syndromic_intellectual_disability|Epilepsy_with_myoclonic_atonic_seizures|SCN2A-related_generalized_epilepsy_with_febrile_seizures_plus|West_syndrome|Autism_spectrum_disorder|Developmental_and_epileptic_encephalopathy|_1|Lennox-Gastaut_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases": 6,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified": 6,
    "Inborn_genetic_diseases|not_specified|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|not_specified|not_provided": 1,
    "Lennox-Gastaut_syndrome|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Episodic_ataxia|_type_9|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11": 5,
    "not_provided|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases": 4,
    "not_specified|Seizures|_benign_familial_infantile|_3|not_provided|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Inborn_genetic_diseases|SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_11|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_11|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|not_provided": 8,
    "Episodic_ataxia|_type_9": 10,
    "not_provided|Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 3,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 12,
    "Myoclonus": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|Inborn_genetic_diseases": 7,
    "SCN2A-related_disorder|Focal_epilepsy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11": 2,
    "Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|History_of_neurodevelopmental_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9": 3,
    "SCN2A-related_disorder": 25,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9": 3,
    "Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3": 1,
    "Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 4,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 9,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder": 3,
    "Seizures|_benign_familial_infantile|_3|Malignant_migrating_partial_seizures_of_infancy": 1,
    "not_provided|West_syndrome": 1,
    "not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases": 3,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Benign_familial_infantile_epilepsy|Seizure": 1,
    "not_specified|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 17,
    "Infantile_spasms": 378,
    "not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 8,
    "West_syndrome|Developmental_and_epileptic_encephalopathy": 8,
    "Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder": 2,
    "Epilepsy|not_provided|Intellectual_disability": 1,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Benign_familial_infantile_epilepsy": 7,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|unclassified_developmental_and_epileptic_encephalopathy|Episodic_ataxia|_type_9|Benign_Neonatal_Epilepsy|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 3,
    "Complex_neurodevelopmental_disorder|Episodic_ataxia|_type_9|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Epileptic_encephalopathy|Infantile_spasms|SCN2A-related_disorder|Inborn_genetic_diseases": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases": 12,
    "West_syndrome": 9,
    "Inborn_genetic_diseases|Autism|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder|not_provided|Developmental_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3": 4,
    "Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "SCN2A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|See_cases": 1,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|not_specified|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder": 3,
    "not_specified|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Inborn_genetic_diseases|Episodic_ataxia|_type_9": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases|not_provided": 6,
    "Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder": 2,
    "Inborn_genetic_diseases|Hemiplegia/hemiparesis": 1,
    "not_specified|SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Autism_spectrum_disorder|unclassified_developmental_and_epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|_infantile_or_early_childhood": 1,
    "SCN2A-related_neurodevelopmental_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_infantile|_3|not_specified|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Movement_disorder|Global_developmental_delay|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Complex_neurodevelopmental_disorder|not_provided": 15,
    "Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Episodic_ataxia|_type_9|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 4,
    "not_specified|Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|Inborn_genetic_diseases": 1,
    "Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 5,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 9,
    "not_specified|Inborn_genetic_diseases|Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|not_provided": 6,
    "Inborn_genetic_diseases|SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus": 10,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified|not_provided": 8,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Complex_neurodevelopmental_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases|not_provided": 4,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|SCN2A-related_disorder": 2,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|See_cases": 1,
    "Episodic_ataxia|_type_9|not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_12": 1328,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified|not_provided": 4,
    "Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 3,
    "not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder": 1,
    "Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified": 2,
    "Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|Inborn_genetic_diseases": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder|Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3": 1,
    "SCN2A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified": 1,
    "Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11": 2,
    "Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9": 6,
    "Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_11|Intellectual_disability|Complex_neurodevelopmental_disorder": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|SCN2A-related_disorder": 1,
    "not_provided|Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Autism_spectrum_disorder|See_cases": 1,
    "Complex_neurodevelopmental_disorder|West_syndrome|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 2,
    "Seizure|not_provided|Complex_neurodevelopmental_disorder|SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_11": 3,
    "Developmental_and_epileptic_encephalopathy|_11|not_provided|Complex_neurodevelopmental_disorder|Seizures|_benign_familial_infantile|_3": 2,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "not_specified|Seizures|_benign_familial_infantile|_3": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder|Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|not_specified": 1,
    "SCN2A-mediated_disorder|Developmental_and_epileptic_encephalopathy|_11|not_provided|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Benign_familial_neonatal-infantile_seizures_1|Developmental_and_epileptic_encephalopathy|_11|Intellectual_disability|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Episodic_ataxia|_type_9|Infantile_spasms": 1,
    "Benign_familial_infantile_epilepsy|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "Complex_neurodevelopmental_disorder|not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Epilepsy_of_infancy_with_migrating_focal_seizures": 1,
    "benign_sporadic_neonatal-infantile_epilepsy": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Inborn_genetic_diseases": 3,
    "Abnormal_cerebral_morphology": 19,
    "SCN2A-related_disorder|not_provided": 2,
    "Seizure|Hereditary_episodic_ataxia|Vertigo|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_30|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder|West_syndrome|SCN2A-related_disorder|not_provided|Epilepsy_of_infancy_with_migrating_focal_seizures": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_11|not_specified": 1,
    "Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder": 2,
    "Complex_neurodevelopmental_disorder|SCN2A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided": 4,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder": 3,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|Inborn_genetic_diseases|not_provided|Genetic_developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Episodic_ataxia|_type_9": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder": 2,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|West_syndrome|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases": 1,
    "Continuous_spikes_and_waves_during_sleep|Seizures|_benign_familial_infantile|_3|Non-syndromic_intellectual_disability|Epilepsy_with_myoclonic_atonic_seizures|SCN2A-related_generalized_epilepsy_with_febrile_seizures_plus|West_syndrome|Autism_spectrum_disorder|Developmental_and_epileptic_encephalopathy|_1|Lennox-Gastaut_syndrome": 1,
    "SCN2A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 2,
    "Intellectual_disability|_autosomal_dominant": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|not_provided": 1,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases": 1,
    "SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|not_specified": 1,
    "Complex_neurodevelopmental_disorder|Benign_familial_infantile_epilepsy|benign_sporadic_infantile_epilepsy|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|not_provided|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_11": 1,
    "not_provided|Malignant_migrating_partial_seizures_of_infancy": 1,
    "not_provided|Dystonia_12": 52,
    "SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3": 1,
    "Epilepsy_of_infancy_with_migrating_focal_seizures|not_provided": 1,
    "West_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_11": 1,
    "not_provided|West_syndrome|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "intellectual_deficiency": 2,
    "Autism_Spectrum_Disorder_with_Intellectual_Disability": 1,
    "not_provided|Inborn_genetic_diseases|SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder": 1,
    "Episodic_ataxia|_type_9|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases|not_specified": 1,
    "Complex_neurodevelopmental_disorder|not_provided|Benign_familial_neonatal-infantile_seizures_1|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|SCN2A-related_generalized_epilepsy_with_febrile_seizures_plus": 1,
    "SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_11|Seizure|not_provided|Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_11|not_provided|Seizures|_benign_familial_infantile|_3": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder": 1,
    "Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)": 3,
    "See_cases|Developmental_and_epileptic_encephalopathy": 2,
    "not_provided|unclassified_developmental_and_epileptic_encephalopathy|Complex_neurodevelopmental_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "SCN2A-associated_neurodevelopmental_disorders|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "Complex_neurodevelopmental_disorder|SCN2A-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder": 1,
    "not_specified|Complex_neurodevelopmental_disorder": 2,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|West_syndrome|Developmental_and_epileptic_encephalopathy": 1,
    "SCN2A-related_disorder|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 2,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 3,
    "SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Epilepsy_of_infancy_with_migrating_focal_seizures|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Developmental_and_epileptic_encephalopathy|not_provided|SCN2A-related_generalized_epilepsy_with_febrile_seizures_plus": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Epilepsy_of_infancy_with_migrating_focal_seizures": 1,
    "not_provided|Developmental_disorder|Complex_neurodevelopmental_disorder|SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "SCN2A-related_disorder|Seizures|_benign_familial_infantile|_3|Seizure": 1,
    "Seizures|_benign_familial_infantile|_3|not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9": 1,
    "not_provided|Episodic_ataxia|_type_9|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_11": 1,
    "SCN2A-related_generalized_epilepsy_with_febrile_seizures_plus": 1,
    "unclassified_developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Seizure|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_provided|Spastic_ataxia": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SCN2A-related_disorder|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified|not_provided": 1,
    "not_provided|SCN2A-related_generalized_epilepsy_with_febrile_seizures_plus|Seizures|_benign_familial_infantile|_3|Complex_neurodevelopmental_disorder": 1,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|West_syndrome|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 2,
    "Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|not_provided|SCN2A-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Global_developmental_delay": 1,
    "benign_sporadic_infantile_epilepsy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided|Inborn_genetic_diseases": 1,
    "SCN2A-related_disorder|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|not_specified|not_provided|Inborn_genetic_diseases|SCN2A-related_disorder": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3": 1,
    "Complex_neurodevelopmental_disorder|Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Episodic_ataxia|_type_9": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Complex_neurodevelopmental_disorder|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases": 1,
    "Seizure|Complex_neurodevelopmental_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_11|Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|West_syndrome|Seizures|_benign_familial_infantile|_3": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|not_specified": 1,
    "Seizures|_benign_familial_infantile|_3|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_11|Seizures|_benign_familial_infantile|_3|Genetic_developmental_and_epileptic_encephalopathy|Episodic_ataxia|_type_9|Developmental_and_epileptic_encephalopathy|_76|Autism|not_provided": 1,
    "SCN2A-related_disorder|Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9|Seizures|_benign_familial_infantile|_3|Inborn_genetic_diseases|not_provided": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|SCN2A-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Seizures|_benign_familial_infantile|_3|SCN2A-related_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_11|Episodic_ataxia|_type_9": 1,
    "Seizures|_benign_familial_infantile|_3|Developmental_and_epileptic_encephalopathy|_11|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Seizures|_benign_familial_infantile|_3": 2,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Seizures|_benign_familial_infantile|_3": 3,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 74,
    "Familial_hyperphosphatemic_tumoral_calcinosis/hyperphosphatemic_hyperostosis_syndrome": 5,
    "not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 34,
    "not_provided|GALNT3-related_disorder|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_1|not_provided": 22,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_1|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1|not_provided": 1,
    "GALNT3-related_disorder": 2,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_1|GALNT3-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 3,
    "Inborn_genetic_diseases|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 1,
    "not_provided|GALNT3-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 2,
    "GALNT3-related_disorder|not_provided": 2,
    "GALNT3-related_disorder|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1|not_provided": 2,
    "not_specified|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 18,
    "Jeune_thoracic_dystrophy|Joubert_syndrome": 6,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 85,
    "Asphyxiating_thoracic_dystrophy_4|not_provided|Nephronophthisis_12": 4,
    "not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 4,
    "Nephronophthisis_12|not_provided|Asphyxiating_thoracic_dystrophy_4": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis": 481,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 21,
    "not_provided|Jeune_thoracic_dystrophy|Nephronophthisis": 10,
    "Nephronophthisis|Jeune_thoracic_dystrophy": 164,
    "Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases|not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|not_provided|not_specified|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis": 28,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Nephronophthisis_12": 15,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 35,
    "Nephronophthisis_12|Nephronophthisis|Jeune_thoracic_dystrophy|not_provided|not_specified|Asphyxiating_thoracic_dystrophy_4": 1,
    "Connective_tissue_disorder|TTC21B-related_disorder": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 2,
    "Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder": 6,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|not_provided|Jeune_thoracic_dystrophy|Nephronophthisis": 2,
    "not_specified|Nephronophthisis|Jeune_thoracic_dystrophy|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Nephronophthisis|Jeune_thoracic_dystrophy": 6,
    "TTC21B-related_disorder|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis": 12,
    "Finnish_congenital_nephrotic_syndrome": 410,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided|Jeune_thoracic_dystrophy|Nephronophthisis": 4,
    "Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Jeune_thoracic_dystrophy|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy": 5,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 2,
    "TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "TTC21B-related_disorder|Nephronophthisis_12": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 3,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephrotic_syndrome": 1,
    "Asphyxiating_thoracic_dystrophy_4|Type_IV_short_rib_polydactyly_syndrome": 1,
    "TTC21B-related_disorder": 20,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_specified": 1,
    "Inborn_genetic_diseases|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 3,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Connective_tissue_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|not_specified|not_provided": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis|Jeune_thoracic_dystrophy|not_provided|not_specified|Connective_tissue_disorder": 1,
    "Nephronophthisis_12|Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_specified": 4,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 11,
    "Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder": 3,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|not_specified": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Inborn_genetic_diseases": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 8,
    "Inborn_genetic_diseases|Nephronophthisis|Jeune_thoracic_dystrophy": 3,
    "Nephronophthisis_12|not_provided|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 2,
    "not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis": 2,
    "not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_4": 3,
    "Inborn_genetic_diseases|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 4,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Inborn_genetic_diseases": 4,
    "Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|not_specified|not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Joubert_syndrome_1|Chronic_kidney_disease": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases": 1,
    "not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis": 3,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|TTC21B-related_disorder": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|not_specified": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|TTC21B-related_disorder": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases": 9,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|Infantile_nephronophthisis|Asphyxiating_thoracic_dystrophy_4": 1,
    "not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_specified|Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Nephronophthisis_12|not_provided": 2,
    "TTC21B-related_disorder|Inborn_genetic_diseases": 2,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 3,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|not_specified": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_specified|Nephronophthisis|Jeune_thoracic_dystrophy|not_provided": 1,
    "not_provided|Nephronophthisis|Jeune_thoracic_dystrophy": 3,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder|Inborn_genetic_diseases": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Nephrotic_syndrome|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|not_specified|Joubert_syndrome": 1,
    "Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases|TTC21B-related_disorder|not_provided": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_specified|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 1,
    "not_specified|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Inborn_genetic_diseases": 1,
    "TTC21B-related_disorder|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_specified|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided": 2,
    "not_provided|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 2,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_specified|not_provided|Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Connective_tissue_disorder|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_specified|not_provided|Joubert_syndrome_1": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|not_provided|TTC21B-related_disorder": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|Asphyxiating_thoracic_dystrophy_4|Meckel-Gruber-like_syndrome|Nephronophthisis_12": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Inborn_genetic_diseases|TTC21B-related_disorder": 1,
    "Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|not_provided|TTC21B-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|not_specified": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|not_specified|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|not_specified": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_4": 1,
    "not_specified|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis": 2,
    "Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|TTC21B-related_disorder": 3,
    "Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder|not_provided": 2,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided|not_specified|Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 2,
    "Asphyxiating_thoracic_dystrophy_4|not_specified|not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided|not_specified": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Connective_tissue_disorder|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Connective_tissue_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_specified": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_specified|not_provided": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_specified|not_provided|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "TTC21B-related_disorder|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 3,
    "Jeune_thoracic_dystrophy|not_provided|Nephronophthisis": 1,
    "Asphyxiating_thoracic_dystrophy_4|not_specified|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|not_provided": 1,
    "Connective_tissue_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_specified|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Type_IV_short_rib_polydactyly_syndrome|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Retinal_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 1,
    "TTC21B-related_disorder|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|Asphyxiating_thoracic_dystrophy_4": 1,
    "TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Renal_dysplasia_and_retinal_aplasia|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis|Jeune_thoracic_dystrophy": 2,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Nephronophthisis": 1,
    "Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Jeune_thoracic_dystrophy": 1,
    "TTC21B-related_disorder|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Inborn_genetic_diseases|not_provided|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_specified|not_provided": 2,
    "Connective_tissue_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Jeune_thoracic_dystrophy|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Nephronophthisis_12": 2,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder": 2,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder|not_provided": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis|Connective_tissue_disorder|not_provided": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 2,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Connective_tissue_disorder|not_specified|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_specified|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided|TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "TTC21B-related_disorder|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|not_specified|not_provided|Joubert_syndrome_1|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Connective_tissue_disorder|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_specified|not_provided": 1,
    "TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|Nephrotic_syndrome|Retinal_dystrophy|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Renal_dysplasia_and_retinal_aplasia|not_provided|Infantile_nephronophthisis|Finnish_congenital_nephrotic_syndrome|See_cases": 1,
    "not_provided|not_specified|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided|Inborn_genetic_diseases": 1,
    "TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|not_provided": 1,
    "not_specified|Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Inborn_genetic_diseases": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "Inborn_genetic_diseases|TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis": 1,
    "not_provided|Jeune_thoracic_dystrophy|Nephronophthisis|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Asphyxiating_thoracic_dystrophy_4|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|TTC21B-related_disorder|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "TTC21B-related_disorder|Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|not_provided": 1,
    "SHORT-RIB_THORACIC_DYSPLASIA_4_WITH_POLYDACTYLY": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Bardet-Biedl_syndrome_2": 1,
    "not_provided|Nephronophthisis|Jeune_thoracic_dystrophy|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Nephronophthisis|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "TTC21B-related_disorder|Nephronophthisis|Jeune_thoracic_dystrophy|not_specified": 1,
    "not_provided|not_specified|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Connective_tissue_disorder|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Joubert_syndrome|Nephronophthisis": 1,
    "not_specified|Nephronophthisis|Jeune_thoracic_dystrophy|Inborn_genetic_diseases|not_provided|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4": 1,
    "Inborn_genetic_diseases|Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis|Jeune_thoracic_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12|Nephronophthisis|Jeune_thoracic_dystrophy|TTC21B-related_disorder|not_provided": 1,
    "Jeune_thoracic_dystrophy|Nephronophthisis|Asphyxiating_thoracic_dystrophy_4|not_provided|Nephronophthisis_12|TTC21B-related_disorder": 1,
    "not_specified|Asphyxiating_thoracic_dystrophy_4|Nephronophthisis_12": 1,
    "Nephronophthisis_12|Asphyxiating_thoracic_dystrophy_4|Jeune_thoracic_dystrophy|Joubert_syndrome": 1,
    "not_provided|Jeune_thoracic_dystrophy|Joubert_syndrome": 1,
    "Migraine|_familial_hemiplegic|_3|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 5,
    "not_provided|Migraine|_familial_hemiplegic|_3|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 7,
    "not_provided|Familial_hemiplegic_migraine|Epilepsy": 1,
    "Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 14,
    "Migraine|_familial_hemiplegic|_3|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 2,
    "Migraine|_familial_hemiplegic|_3|Epilepsy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Epilepsy|not_provided": 1,
    "Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 2,
    "Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Epilepsy|Migraine|_familial_hemiplegic|_3": 2,
    "Epilepsy|Familial_hemiplegic_migraine": 2,
    "Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_provided": 1,
    "Epilepsy|not_provided|Familial_hemiplegic_migraine": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 100,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 2,
    "Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy": 15,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder": 3,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|See_cases|Developmental_and_epileptic_encephalopathy": 2,
    "Inborn_genetic_diseases|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy": 7,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy": 9,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 7,
    "not_provided|SCN1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|West_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 12,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B": 4,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy": 18,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Febrile_seizures|_familial|_1|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 5,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy": 26,
    "Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy": 24,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Inborn_genetic_diseases": 1,
    "Migraine|_familial_hemiplegic|_3|Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Seizure": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 81,
    "not_provided|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|See_cases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_6A|not_provided": 1,
    "SCN1A-related_disorder|not_specified|Mitochondrial_disease|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Developmental_and_epileptic_encephalopathy": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 12,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Seizure|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 8,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Severe_myoclonic_epilepsy_in_infancy": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy": 7,
    "Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|SCN1A_Seizure_Disorders|Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|SCN1A-related_epilepsy_syndrome|_recessive": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "SCN1A-related_disorder": 11,
    "Developmental_and_epileptic_encephalopathy_6B": 19,
    "Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy": 5,
    "not_provided|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 11,
    "SCN1A-related_channelopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|SCN1A-related_disorder": 1,
    "not_provided|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 4,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_specified|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 3,
    "not_specified|Developmental_and_epileptic_encephalopathy|Autosomal_dominant_epilepsy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B": 4,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3": 1,
    "Autosomal_dominant_epilepsy": 8,
    "Developmental_and_epileptic_encephalopathy|Autosomal_dominant_epilepsy|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "SCN1A_Seizure_Disorders|not_provided": 1,
    "Focal-onset_seizure": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 9,
    "Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "SCN1A-related_disorder|not_specified|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy": 1,
    "Migraine|_familial_hemiplegic|_3": 17,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 7,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 2,
    "Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Focal_epilepsy|not_provided|Autism|Microcephaly|Focal-onset_seizure|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 2,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided|Autosomal_dominant_epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "Migraine|_familial_hemiplegic|_3|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|SCN1A-related_disorder": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Macrocephaly_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 31,
    "Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 2,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 2,
    "Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy|Focal_epilepsy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 29,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Microcephaly|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 2,
    "Focal_epilepsy|not_provided|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy": 2,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Seizure": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Epilepsy|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy": 4,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "not_specified|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 5,
    "Developmental_and_epileptic_encephalopathy|not_provided|Migraine|_familial_hemiplegic|_3": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Myoclonic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_76|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Inborn_genetic_diseases|not_specified|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Sudden_unexplained_death_in_childhood": 3,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|See_cases": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 34,
    "not_provided|Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 4,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Acute_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified": 16,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 2,
    "not_provided|Migraine|_familial_hemiplegic|_3": 2,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 3,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 2,
    "SCN1A_Seizure_Disorders": 2,
    "not_provided|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy": 3,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy": 1,
    "Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Epilepsy|Developmental_and_epileptic_encephalopathy": 3,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_3|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy": 2,
    "Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Severe_myoclonic_epilepsy_in_infancy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Seizure|Developmental_and_epileptic_encephalopathy": 7,
    "Developmental_and_epileptic_encephalopathy_6B|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 5,
    "Severe_myoclonic_epilepsy_in_infancy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3": 3,
    "Developmental_and_epileptic_encephalopathy|_6A|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "SCN1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Severe_myoclonic_epilepsy_in_infancy|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Developmental_and_epileptic_encephalopathy": 1,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Primary_generalized_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 3,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_6A": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_6B": 4,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Seizure": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|SCN1A-related_disorder|not_provided|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|not_provided": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "SCN1A-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|Seizure": 2,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "not_provided|pharmacoresistant_multifocal_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "not_provided|not_specified|Epilepsy|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Seizure|Bilateral_tonic-clonic_seizure|Generalized_non-motor_(absence)_seizure": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided": 4,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy_6B": 3,
    "SCN1A-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 7,
    "Developmental_and_epileptic_encephalopathy|Seizure": 5,
    "Developmental_and_epileptic_encephalopathy_6B|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "SCN1A-related_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|Weaver_syndrome": 1,
    "SCN1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Autism": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 4,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|SCN1A-related_disorder": 3,
    "Inborn_genetic_diseases|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 2,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Abnormality_of_the_nervous_system|Atypical_behavior|Global_developmental_delay|Gait_disturbance|Aggressive_behavior|Impulsivity|Intellectual_disability|SCN1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Epilepsy": 1,
    "Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 3,
    "Developmental_and_epileptic_encephalopathy|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "SCN1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 4,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|not_provided|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Inborn_genetic_diseases": 11,
    "Developmental_and_epileptic_encephalopathy_6B|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided|Seizure": 1,
    "Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|not_provided": 1,
    "Autosomal_dominant_epilepsy|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Seizure": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Epilepsy|not_provided|Migraine|_familial_hemiplegic|_3": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "Febrile_seizures|_familial|_1|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|Inborn_genetic_diseases": 1,
    "not_provided|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy": 2,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "not_provided|Epilepsy|Familial_hemiplegic_migraine": 1,
    "Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Familial_hemiplegic_migraine|not_specified|not_provided|Epilepsy": 1,
    "Inborn_genetic_diseases|SCN1A-related_disorder|Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|_1|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Inborn_genetic_diseases|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|Epilepsy|not_provided|Developmental_and_epileptic_encephalopathy|Familial_hemiplegic_migraine": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Autosomal_dominant_epilepsy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Seizure": 3,
    "Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Intellectual_disability|Developmental_and_epileptic_encephalopathy": 2,
    "Myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "not_provided|Epilepsy|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Generalized_epilepsy|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Inborn_genetic_diseases|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 1,
    "not_provided|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|SCN1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_provided|Developmental_and_epileptic_encephalopathy|Epilepsy|not_specified": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|SCN1A-related_disorder|Epilepsy|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Autism|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder|not_specified|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy": 1,
    "SCN1A-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Early-infantile_DEE": 1,
    "SCN1A-related_disorder|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_epilepsy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy": 3,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Epilepsy": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy": 2,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided|Intellectual_disability|_mild|Seizure": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B": 2,
    "Epilepsy|not_specified|Familial_hemiplegic_migraine|Developmental_and_epileptic_encephalopathy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Severe_myoclonic_epilepsy_in_infancy|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|Seizure|See_cases": 1,
    "Developmental_and_epileptic_encephalopathy|_6A|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_6A|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Congenital_contracture|Knee_flexion_contracture|Camptodactyly_of_2nd-5th_fingers|Hip_contracture|Anterior_creases_of_earlobe|Clinodactyly|not_provided|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Febrile_seizures|_familial|_3a": 1,
    "not_provided|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|not_provided|Severe_myoclonic_epilepsy_in_infancy|Intellectual_disability": 1,
    "not_provided|Obesity|Seizure|Intellectual_disability": 1,
    "Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Familial_hemiplegic_migraine": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B": 1,
    "Neonatal_developmental_and_epileptic_encephalopathy_with_movement_disorders_and_arthrogryposis_(NDEEMA)": 1,
    "SCN1A_Seizure_Disorders|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|_6A|Developmental_and_epileptic_encephalopathy_6B|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|not_provided|Seizure|Global_developmental_delay": 1,
    "Febrile_seizures|_familial|_3a|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_SCN1A-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_6A": 1,
    "Developmental_and_epileptic_encephalopathy|Seizure|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_specified": 1,
    "Febrile_seizures|_familial|_3a|carbamazepine_response_-_Dosage|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Migraine|_familial_hemiplegic|_3|not_specified": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Developmental_and_epileptic_encephalopathy": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy|_76|Developmental_and_epileptic_encephalopathy|not_provided|Focal_impaired_awareness_seizure|See_cases|Seizure|Autism|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Febrile_seizures|_familial|_3a|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Autosomal_dominant_epilepsy|not_provided|Seizure": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Severe_myoclonic_epilepsy_in_infancy|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Developmental_and_epileptic_encephalopathy_6B|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|not_provided|Febrile_seizures|_familial|_3a": 1,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|SCN1A-related_disorder": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Migraine|_familial_hemiplegic|_3|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Epilepsy|not_specified": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|Familial_hemiplegic_migraine": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Epilepsy|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "Severe_myoclonic_epilepsy_in_infancy|not_provided|SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Developmental_and_epileptic_encephalopathy_6B|Developmental_and_epileptic_encephalopathy|not_provided|Migraine|_familial_hemiplegic|_3": 1,
    "Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|Severe_myoclonic_epilepsy_in_infancy|Febrile_seizures|_familial|_1|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided|Developmental_and_epileptic_encephalopathy|Severe_myoclonic_epilepsy_in_infancy|Migraine|_familial_hemiplegic|_3": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Migraine|_familial_hemiplegic|_3|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "SCN1A-related_disorder|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_6B|Migraine|_familial_hemiplegic|_3|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_2|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified": 6,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 6,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 8,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 8,
    "Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Inherited_Erythromelalgia|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 2,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 3,
    "Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 5,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 3,
    "Inherited_Erythromelalgia|not_provided|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder|Congenital_Indifference_to_Pain|Febrile_seizures|_familial|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 2,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 5,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 11,
    "Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 3,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 1,
    "Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided": 1,
    "Inherited_Erythromelalgia|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 3,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided|Primary_erythromelalgia": 1,
    "not_provided|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "Febrile_seizures|_familial|Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 1,
    "not_provided|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Propofol_response": 1,
    "not_provided|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|Primary_erythromelalgia|not_provided": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder|Febrile_seizures|_familial|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Small_fiber_neuropathy": 1,
    "Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder": 2,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inherited_Erythromelalgia|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "Inherited_Erythromelalgia|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Congenital_Indifference_to_Pain": 3,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 6,
    "Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Small_fiber_neuropathy|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|Primary_erythromelalgia": 3,
    "Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder|Febrile_seizures|_familial|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 2,
    "Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy": 1,
    "Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 2,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Congenital_Indifference_to_Pain": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided|Primary_erythromelalgia": 1,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_provided": 1,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_provided": 1,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Febrile_seizures|_familial|Paroxysmal_extreme_pain_disorder|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 1,
    "Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided|Primary_erythromelalgia": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 33,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 534,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1368,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 50,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 12,
    "not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Severe_myoclonic_epilepsy_in_infancy|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inborn_genetic_diseases|not_specified|Paroxysmal_extreme_pain_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 74,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 20,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 9,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Severe_myoclonic_epilepsy_in_infancy|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 3,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 21,
    "not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Inborn_genetic_diseases": 1,
    "Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Primary_erythromelalgia": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Small_fiber_neuropathy|not_specified|not_provided": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 9,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 33,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|not_specified|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 22,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 13,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia": 3,
    "Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 4,
    "Inborn_genetic_diseases|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 2,
    "Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Primary_erythromelalgia": 17,
    "not_specified|not_provided|SCN9A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified": 9,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 17,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "not_provided|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 5,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 6,
    "not_specified|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Paroxysmal_extreme_pain_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 4,
    "not_provided|Paroxysmal_extreme_pain_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_specified|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided": 5,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 2,
    "Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder": 1,
    "not_specified|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_specified|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|SCN9A-related_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Paroxysmal_extreme_pain_disorder": 6,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|SCN9A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|SCN9A-related_disorder": 2,
    "Charcot-Marie-Tooth_disease|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder|Febrile_seizures|_familial|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 6,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Inherited_Erythromelalgia|Inborn_genetic_diseases|Primary_erythromelalgia|SCN9A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Febrile_seizures|_familial|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 27,
    "Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 2,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 2,
    "Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Primary_erythromelalgia": 1,
    "Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_provided": 8,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 4,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Inborn_genetic_diseases": 2,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|SCN9A-related_disorder": 1,
    "Primary_erythromelalgia|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 4,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Generalized_epilepsy_with_febrile_seizures_plus|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Inborn_genetic_diseases": 4,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_provided": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_IId|Charcot-Marie-Tooth_disease": 1,
    "SCN9A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Small_fiber_neuropathy|not_provided|not_specified|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inherited_Erythromelalgia|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_ataxia|not_specified|not_provided": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Primary_erythromelalgia|Small_fiber_neuropathy|not_specified|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "not_provided|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Inborn_genetic_diseases": 1,
    "Primary_erythromelalgia|Severe_myoclonic_epilepsy_in_infancy|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|SCN9A-related_disorder|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|SCN9A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Severe_myoclonic_epilepsy_in_infancy|Febrile_seizures|_familial|Congenital_Indifference_to_Pain|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 1,
    "Primary_erythromelalgia|Inborn_genetic_diseases|not_provided|Paroxysmal_extreme_pain_disorder|See_cases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "not_specified|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia": 1,
    "Small_fiber_neuropathy|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|Febrile_seizures|_familial|not_provided|Small_fiber_neuropathy|Inherited_Erythromelalgia|Congenital_Indifference_to_Pain|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_specified": 1,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Small_fiber_neuropathy|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided": 1,
    "Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Generalized_non-motor_(absence)_seizure|Abnormal_brainstem_MRI_signal_intensity": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_provided|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Paroxysmal_extreme_pain_disorder": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|SCN9A-related_disorder": 1,
    "Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "SCN9A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|SCN9A-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|SCN9A-related_disorder": 1,
    "SCN9A-related_disorder": 5,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_specified|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|SCN9A-related_disorder|not_provided": 1,
    "Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Paroxysmal_extreme_pain_disorder|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|not_specified|not_provided|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|SCN9A-related_disorder|not_provided": 1,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Febrile_seizures|_familial|Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Congenital_Indifference_to_Pain|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 1,
    "Inherited_Erythromelalgia|Congenital_Indifference_to_Pain|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "SCN9A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Inborn_genetic_diseases|Small_fiber_neuropathy|Primary_erythromelalgia|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Autism_spectrum_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_specified": 2,
    "Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "SCN9A-related_peripheral_neuropathies_associated_with_increased_pain|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Primary_erythromelalgia|Abnormality_of_pain_sensation|Acute_episodes_of_neuropathic_symptoms": 1,
    "not_specified|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Small_fiber_neuropathy|not_specified|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|SCN9A-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inherited_Erythromelalgia|not_provided|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inherited_Erythromelalgia|not_specified|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided|Primary_erythromelalgia": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_specified|not_provided|Inherited_Erythromelalgia": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Severe_myoclonic_epilepsy_in_infancy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|Paroxysmal_extreme_pain_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|SCN9A-related_disorder|Inherited_Erythromelalgia|Inborn_genetic_diseases|not_specified|not_provided|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 3,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 2,
    "Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Inborn_genetic_diseases|not_provided|not_specified|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Paroxysmal_extreme_pain_disorder|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Primary_erythromelalgia": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|SCN9A-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Small_fiber_neuropathy": 1,
    "not_specified|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Primary_erythromelalgia": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Primary_erythromelalgia": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Inborn_genetic_diseases|Severe_myoclonic_epilepsy_in_infancy|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 1,
    "SCN9A-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Seizure|Global_developmental_delay|Hypoglycemia": 1,
    "Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Inborn_genetic_diseases|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inherited_Erythromelalgia|Congenital_Indifference_to_Pain|Febrile_seizures|_familial|Severe_myoclonic_epilepsy_in_infancy|Primary_erythromelalgia|not_provided|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder": 1,
    "Congenital_Indifference_to_Pain|Febrile_seizures|_familial|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|Generalized_epilepsy_with_febrile_seizures_plus|Small_fiber_neuropathy|Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "SCN9A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 3,
    "Small_fiber_neuropathy|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Inborn_genetic_diseases|SCN9A-related_neuropathic_pain_syndromes|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Generalized_epilepsy_with_febrile_seizures_plus|Self-limited_epilepsy_with_centrotemporal_spikes|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inherited_Erythromelalgia|Inborn_genetic_diseases|not_provided|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|Primary_erythromelalgia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Paroxysmal_extreme_pain_disorder": 1,
    "Pain_insensitivity|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 2,
    "Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Severe_myoclonic_epilepsy_in_infancy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Congenital_Indifference_to_Pain|Small_fiber_neuropathy|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "SCN9A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided|Small_fiber_neuropathy|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Seizure": 1,
    "Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Inborn_genetic_diseases|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Small_fiber_neuropathy|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_provided|not_specified": 1,
    "SCN9A-related_disorder|Inherited_Erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|SCN9A-related_disorder|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus": 1,
    "Primary_erythromelalgia|Small_fiber_neuropathy|not_specified|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 2,
    "Primary_erythromelalgia|Febrile_seizures|_familial|_1|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Severe_myoclonic_epilepsy_in_infancy|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "Primary_erythromelalgia|not_specified|Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Severe_myoclonic_epilepsy_in_infancy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Small_fiber_neuropathy|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "not_provided|Paroxysmal_extreme_pain_disorder|Inherited_Erythromelalgia|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Primary_erythromelalgia": 1,
    "SCN9A-related_disorder|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|SCN9A-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "SCN9A-related_disorder|Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|not_provided|SCN9A-related_disorder": 1,
    "not_specified|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_provided|Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|SCN9A-related_disorder|Inborn_genetic_diseases|not_specified|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "not_specified|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|SCN9A-related_disorder|not_specified": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|Inborn_genetic_diseases": 2,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 2,
    "Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|not_specified": 1,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|Paroxysmal_extreme_pain_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases|SCN9A-related_disorder|not_specified": 1,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_specified|Small_fiber_neuropathy|not_provided": 1,
    "not_provided|SCN9A-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Small_fiber_neuropathy|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Severe_myoclonic_epilepsy_in_infancy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|SCN9A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Primary_erythromelalgia|Inborn_genetic_diseases": 1,
    "not_specified|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|not_provided": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B": 727,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Febrile_seizures|_familial|_3b": 1,
    "not_specified|Primary_erythromelalgia|Small_fiber_neuropathy|not_provided|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Inborn_genetic_diseases|Epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Inborn_genetic_diseases|Inherited_Erythromelalgia|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Small_fiber_neuropathy|Inborn_genetic_diseases|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 1,
    "Primary_erythromelalgia|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Severe_myoclonic_epilepsy_in_infancy|Paroxysmal_extreme_pain_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided|not_specified|Febrile_seizures|_familial|_3b": 1,
    "Small_fiber_neuropathy|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Small_fiber_neuropathy|Inborn_genetic_diseases|not_provided|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|SCN9A-related_disorder|Primary_erythromelalgia": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_provided": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia|Inherited_Erythromelalgia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "not_provided|Primary_erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Generalized_epilepsy_with_febrile_seizures_plus|_type_7": 1,
    "Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive": 1,
    "Primary_erythromelalgia|Small_fiber_neuropathy|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "not_provided|Inherited_Erythromelalgia|Paroxysmal_extreme_pain_disorder|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Primary_erythromelalgia": 1,
    "not_provided|Small_fiber_neuropathy|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder": 1,
    "Inherited_Erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Paroxysmal_extreme_pain_disorder|not_provided|Primary_erythromelalgia": 1,
    "Paroxysmal_extreme_pain_disorder|Primary_erythromelalgia|Channelopathy-associated_congenital_insensitivity_to_pain|_autosomal_recessive|Small_fiber_neuropathy": 2,
    "SCN7A-related_disorder": 12,
    "SCN7A-related_disorder|not_provided": 4,
    "not_provided|SCN7A-related_disorder": 6,
    "not_specified|SCN7A-related_disorder": 1,
    "XIRP2-related_disorder": 60,
    "not_provided|XIRP2-related_disorder": 30,
    "XIRP2-related_disorder|not_provided": 9,
    "not_specified|not_provided|XIRP2-related_disorder": 2,
    "Blepharophimosis|Congenital_heart_defects|_multiple_types|_4": 1,
    "not_provided|XIRP2-related_disorder|not_specified": 1,
    "G6PC2-related_disorder": 5,
    "not_provided|Fasting_plasma_glucose_level_quantitative_trait_locus_1": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2": 205,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 39,
    "Progressive_familial_intrahepatic_cholestasis": 12,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 6,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 10,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 13,
    "Benign_recurrent_intrahepatic_cholestasis_type_2": 33,
    "ABCB11-related_disorder|not_provided": 26,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided": 4,
    "Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|not_provided": 4,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 5,
    "Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_2": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 50,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 7,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2": 8,
    "Familial_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder": 27,
    "Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 5,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "not_provided|ABCB11-related_disorder": 18,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_2": 3,
    "not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 7,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis": 3,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_specified": 4,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Benign_recurrent_intrahepatic_cholestasis_type_2": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 20,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 4,
    "not_provided|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2": 3,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided": 3,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis|ABCB11-related_disorder|not_provided": 1,
    "Familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 3,
    "not_specified|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis": 2,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|not_specified": 7,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|not_specified": 4,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|Abnormal_liver_function_tests_during_pregnancy|Pruritus|Intrahepatic_cholestasis|not_provided": 1,
    "Inborn_genetic_diseases|ABCB11-related_disorder": 1,
    "ABCB11-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|not_specified": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_specified|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder|not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 3,
    "not_specified|ABCB11-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 1,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis|not_provided": 1,
    "not_specified|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|ABCB11-related_disorder": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|not_specified": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2": 10,
    "not_provided|ABCB11-related_disorder|not_specified": 1,
    "not_specified|Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_specified|not_provided": 4,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|not_specified": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided": 9,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Inborn_genetic_diseases": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis": 1,
    "ABCB11-related_disorder|not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 1,
    "not_specified|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 3,
    "ABCB11-related_disorder|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "not_provided|not_specified|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis|not_provided": 1,
    "ABCB11-related_disorder|not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_specified|Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided": 1,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|not_specified|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|ABCB11-related_disorder": 1,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis|Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "not_provided|ABCB11-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder|not_provided|not_specified": 2,
    "not_provided|not_specified|Progressive_familial_intrahepatic_cholestasis_type_2": 3,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis": 1,
    "ABCB11-related_disorder|See_cases|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_specified|not_provided|ABCB11-related_disorder": 1,
    "ABCB11-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|not_specified": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3": 28,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 1,
    "ABCB11-related_disorder|not_provided|not_specified|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis|not_provided": 1,
    "ABCB11-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 3,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|not_specified": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Cholestasis|_intrahepatic|_of_pregnancy|_3|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_4|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis|not_provided|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_specified|ABCB11-related_disorder": 1,
    "not_provided|not_specified|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Inborn_genetic_diseases": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|not_specified": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|not_provided|not_specified": 1,
    "Progressive_familial_intrahepatic_cholestasis|Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder": 1,
    "not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder|Familial_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Benign_recurrent_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "ABCB11-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Inborn_genetic_diseases|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_2": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|ABCB11-related_disorder": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|Benign_recurrent_intrahepatic_cholestasis_type_2|not_specified|not_provided": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_2|not_provided|Progressive_familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis": 1,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|ABCB11-related_disorder|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_2|not_provided|Inborn_genetic_diseases|Benign_recurrent_intrahepatic_cholestasis_type_2": 1,
    "Donnai-Barrow_syndrome": 390,
    "Donnai-Barrow_syndrome|not_provided": 223,
    "not_provided|Donnai-Barrow_syndrome": 302,
    "not_provided|Donnai-Barrow_syndrome|Inborn_genetic_diseases": 23,
    "LRP2-related_disorder|not_provided": 29,
    "Donnai-Barrow_syndrome|not_provided|Inborn_genetic_diseases|LRP2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Donnai-Barrow_syndrome": 31,
    "not_provided|LRP2-related_disorder": 23,
    "not_provided|not_specified|Donnai-Barrow_syndrome": 10,
    "Inborn_genetic_diseases|Donnai-Barrow_syndrome|not_provided": 20,
    "Donnai-Barrow_syndrome|Inborn_genetic_diseases": 14,
    "not_provided|Prolactin-producing_pituitary_gland_adenoma|High_myopia|Inborn_genetic_diseases": 1,
    "LRP2-related_disorder|not_specified|not_provided|Donnai-Barrow_syndrome": 5,
    "Inborn_genetic_diseases|not_provided|Donnai-Barrow_syndrome|LRP2-related_disorder": 1,
    "not_provided|Donnai-Barrow_syndrome|LRP2-related_disorder|not_specified": 1,
    "not_provided|Donnai-Barrow_syndrome|LRP2-related_disorder": 10,
    "Donnai-Barrow_syndrome|Inborn_genetic_diseases|not_provided": 19,
    "not_specified|not_provided|Donnai-Barrow_syndrome": 30,
    "not_specified|Donnai-Barrow_syndrome|not_provided": 14,
    "Inborn_genetic_diseases|Donnai-Barrow_syndrome": 9,
    "LRP2-related_disorder": 14,
    "not_provided|LRP2-related_disorder|Donnai-Barrow_syndrome": 8,
    "not_provided|LRP2-related_disorder|not_specified|Donnai-Barrow_syndrome|Intellectual_disability": 1,
    "LRP2-related_disorder|not_provided|Donnai-Barrow_syndrome": 15,
    "Donnai-Barrow_syndrome|Inborn_genetic_diseases|LRP2-related_disorder|not_specified|not_provided": 1,
    "Donnai-Barrow_syndrome|not_provided|Inborn_genetic_diseases": 12,
    "Donnai-Barrow_syndrome|not_specified|not_provided": 5,
    "LRP2-related_disorder|Intellectual_disability|Donnai-Barrow_syndrome|not_provided": 1,
    "Donnai-Barrow_syndrome|not_provided|not_specified": 5,
    "Donnai-Barrow_syndrome|Intellectual_disability|not_provided": 2,
    "not_provided|LRP2-related_disorder|Donnai-Barrow_syndrome|DSD_incomplete_virilization|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Donnai-Barrow_syndrome": 1,
    "LRP2-related_disorder|Inborn_genetic_diseases|not_provided|Donnai-Barrow_syndrome": 4,
    "Inborn_genetic_diseases|LRP2-related_disorder|not_provided|Donnai-Barrow_syndrome": 1,
    "Donnai-Barrow_syndrome|LRP2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Donnai-Barrow_syndrome": 25,
    "Donnai-Barrow_syndrome|LRP2-related_disorder|not_provided": 8,
    "Inborn_genetic_diseases|DSD_incomplete_virilization|not_provided|LRP2-related_disorder|not_specified|Donnai-Barrow_syndrome": 1,
    "LRP2-related_disorder|Donnai-Barrow_syndrome": 1,
    "not_provided|LRP2-related_disorder|Inborn_genetic_diseases|Donnai-Barrow_syndrome": 1,
    "LRP2-related_disorder|not_specified|Donnai-Barrow_syndrome|not_provided": 1,
    "not_provided|Donnai-Barrow_syndrome|LRP2-related_disorder|Inborn_genetic_diseases": 1,
    "Donnai-Barrow_syndrome|not_provided|LRP2-related_disorder": 6,
    "LRP2-related_disorder|Donnai-Barrow_syndrome|not_provided": 9,
    "Intellectual_disability|Donnai-Barrow_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Donnai-Barrow_syndrome|not_provided|not_specified": 1,
    "Donnai-Barrow_syndrome|not_provided|Intellectual_disability": 1,
    "Stickler_syndrome": 6,
    "not_specified|not_provided|Hearing_impairment": 5,
    "Congenital_heart_disease|not_provided|Donnai-Barrow_syndrome": 1,
    "Inborn_genetic_diseases|LRP2-related_disorder|Donnai-Barrow_syndrome|not_provided": 1,
    "not_provided|Donnai-Barrow_syndrome|not_specified": 10,
    "LRP2-related_disorder|not_provided|Inborn_genetic_diseases|Donnai-Barrow_syndrome": 1,
    "LRP2-related_disorder|Donnai-Barrow_syndrome|Intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "LRP2-related_disorder|not_provided|DSD_incomplete_virilization|Inborn_genetic_diseases|Donnai-Barrow_syndrome": 1,
    "not_specified|not_provided|Donnai-Barrow_syndrome|LRP2-related_disorder": 1,
    "not_provided|Donnai-Barrow_syndrome|Intellectual_disability": 1,
    "Donnai-Barrow_syndrome|LRP2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "DSD_incomplete_virilization|not_provided|not_specified": 1,
    "Donnai-Barrow_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "LRP2-related_disorder|Donnai-Barrow_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hearing_loss_and_Retinal_dystrophy|Intellectual_disability|Inborn_genetic_diseases|not_provided|Donnai-Barrow_syndrome": 1,
    "Donnai-Barrow_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Donnai-Barrow_syndrome|Non-syndromic_syndactyly": 1,
    "not_specified|not_provided|Donnai-Barrow_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Donnai-Barrow_syndrome|not_specified": 1,
    "LRP2-related_disorder|not_provided|Intellectual_disability": 1,
    "not_specified|LRP2-related_disorder|not_provided|Donnai-Barrow_syndrome": 1,
    "not_provided|not_specified|LRP2-related_disorder|Donnai-Barrow_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|LRP2-related_disorder|Donnai-Barrow_syndrome": 1,
    "LRP2-related_disorder|not_provided|not_specified|Donnai-Barrow_syndrome": 1,
    "LRP2-related_disorder|not_specified|not_provided|Donnai-Barrow_syndrome|Intellectual_disability": 1,
    "Donnai-Barrow_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Donnai-Barrow_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Donnai-Barrow_syndrome|not_provided|LRP2-related_disorder": 1,
    "Donnai-Barrow_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|LRP2-related_disorder": 1,
    "Cardiac|_facial|_and_digital_anomalies_with_developmental_delay": 28,
    "LRP2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hearing_loss_and_Retinal_dystrophy|Donnai-Barrow_syndrome": 1,
    "Donnai-Barrow_syndrome|not_provided|not_specified|LRP2-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome_5|not_specified": 1,
    "BBS5-related_disorder": 28,
    "BBS5-related_disorder|not_specified": 1,
    "Bardet-Biedl_syndrome_5": 38,
    "Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome": 10,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5": 20,
    "BBS5-related_disorder|Bardet-Biedl_syndrome": 11,
    "Bardet-Biedl_syndrome_5|Inborn_genetic_diseases|BBS5-related_disorder|Bardet-Biedl_syndrome|not_specified|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome|BBS5-related_disorder": 1,
    "Bardet-Biedl_syndrome|BBS5-related_disorder": 14,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5|BBS5-related_disorder": 2,
    "Bardet-Biedl_syndrome|BBS5-related_disorder|Bardet-Biedl_syndrome_5": 5,
    "BBS5-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5": 2,
    "Bardet-Biedl_syndrome_5|not_provided|Bardet-Biedl_syndrome|BBS5-related_disorder": 1,
    "BBS5-related_disorder|Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome|not_specified|BBS5-related_disorder": 2,
    "Bardet-Biedl_syndrome_5|not_provided|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome|BBS5-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|BBS5-related_disorder": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 39,
    "not_provided|BBS5-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5": 1,
    "not_provided|Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|not_specified": 4,
    "Cone_dystrophy|BBS5-related_disorder": 1,
    "Bardet-Biedl_syndrome_5|BBS5-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_5": 1,
    "Retinal_dystrophy|not_specified|not_provided|Bardet-Biedl_syndrome|Cone_dystrophy|Intellectual_disability": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome": 4,
    "Bardet-Biedl_syndrome_5|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_5|BBS5-related_disorder|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5|BBS5-related_disorder": 2,
    "not_specified|Bardet-Biedl_syndrome": 19,
    "Bardet-Biedl_syndrome|Intellectual_disability|Bardet-Biedl_syndrome_5|BBS5-related_disorder|not_specified|not_provided": 1,
    "BBS5-related_disorder|Bardet-Biedl_syndrome_5|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "BBS5-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5": 1,
    "BBS5-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Cone_dystrophy|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_5|Retinal_dystrophy": 1,
    "not_provided|Bardet-Biedl_syndrome_5": 1,
    "not_provided|not_specified|Nemaline_myopathy_9": 1,
    "Nemaline_myopathy_9": 206,
    "not_provided|KLHL41-related_disorder|Nemaline_myopathy_9": 3,
    "not_provided|Nemaline_myopathy_9|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_9": 15,
    "Nemaline_myopathy_9|Inborn_genetic_diseases|not_provided": 2,
    "Nemaline_myopathy_9|Inborn_genetic_diseases": 14,
    "KLHL41-related_disorder|Nemaline_myopathy_9|not_provided": 1,
    "not_provided|Nemaline_myopathy_9": 9,
    "Nemaline_myopathy_9|not_provided": 11,
    "Nemaline_myopathy|Nemaline_myopathy_9": 1,
    "Nemaline_myopathy_9|KLHL41-related_disorder": 3,
    "not_specified|not_provided|Nemaline_myopathy_9": 3,
    "Inborn_genetic_diseases|KLHL41-related_disorder|Nemaline_myopathy_9": 1,
    "not_provided|Nemaline_myopathy_9|not_specified": 1,
    "not_specified|Nemaline_myopathy_9|not_provided": 1,
    "Glaucoma_1|_open_angle|_B": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_72": 10,
    "Intellectual_developmental_disorder|_autosomal_recessive_72|not_provided|Intellectual_disability|_severe": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_72|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_72|Intellectual_disability|_severe": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_72": 1,
    "METTL5-related_disorder": 1,
    "UBR3-related_disorder": 21,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|not_provided": 8,
    "Spastic_quadriplegic_cerebral_palsy": 3,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Inborn_genetic_diseases": 7,
    "GAD1-related_disorder": 3,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Infantile_spasms": 1,
    "Developmental_and_epileptic_encephalopathy_89": 14,
    "Developmental_and_epileptic_encephalopathy_89|not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 3,
    "GAD1-related_disorder|not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 1,
    "Developmental_and_epileptic_encephalopathy_89|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities": 1,
    "Inborn_genetic_diseases|GAD1-related_disorder|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|not_provided": 1,
    "Pyridoxine-dependent_epilepsy|Refractory_epilepsy": 1,
    "GAD1-related_disorder|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|not_provided|Hereditary_spastic_paraplegia": 1,
    "GAD1-related_disorder|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy_89": 1,
    "not_provided|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_white_matter_abnormalities|Inborn_genetic_diseases": 1,
    "Woodhouse-Sakati_syndrome": 404,
    "not_provided|Woodhouse-Sakati_syndrome": 15,
    "Inborn_genetic_diseases|Woodhouse-Sakati_syndrome": 11,
    "Woodhouse-Sakati_syndrome|DCAF17-related_disorder": 2,
    "Woodhouse-Sakati_syndrome|Inborn_genetic_diseases": 7,
    "Woodhouse-Sakati_syndrome|not_provided": 12,
    "Woodhouse-Sakati_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Woodhouse-Sakati_syndrome": 2,
    "not_provided|DCAF17-related_disorder|Woodhouse-Sakati_syndrome": 1,
    "DCAF17-related_disorder": 1,
    "DCAF17-related_disorder|Woodhouse-Sakati_syndrome": 5,
    "not_specified|not_provided|Woodhouse-Sakati_syndrome": 3,
    "Woodhouse-Sakati_syndrome|DCAF17-related_disorder|not_provided": 1,
    "Woodhouse-Sakati_syndrome|not_specified": 2,
    "DCAF17-related_disorder|not_provided|Woodhouse-Sakati_syndrome": 2,
    "Woodhouse-Sakati_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Woodhouse-Sakati_syndrome|Inborn_genetic_diseases|not_provided|DCAF17-related_disorder": 1,
    "not_provided|not_specified|Woodhouse-Sakati_syndrome": 4,
    "DCAF17-related_disorder|Woodhouse-Sakati_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Woodhouse-Sakati_syndrome": 1,
    "not_provided|Woodhouse-Sakati_syndrome|DCAF17-related_disorder": 1,
    "not_provided|Woodhouse-Sakati_syndrome|not_specified": 1,
    "DCAF17-related_disorder|not_specified|Woodhouse-Sakati_syndrome": 1,
    "Woodhouse-Sakati_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Woodhouse-Sakati_syndrome": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Woodhouse-Sakati_syndrome": 1,
    "CYBRD1-related_disorder": 2,
    "Neurodevelopmental_disorder_with_microcephaly_and_structural_brain_anomalies": 5,
    "DYNC1I2-related_disorder": 5,
    "Neurodevelopmental_disorder_with_microcephaly_and_structural_brain_anomalies|Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_variable_brain_anomalies|Neurodevelopmental_disorder_with_microcephaly_and_structural_brain_anomalies": 1,
    "Developmental_and_epileptic_encephalopathy|_39": 18,
    "SLC25A12-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_39": 1,
    "SLC25A12-related_disorder|not_provided": 5,
    "not_provided|SLC25A12-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy|_39|SLC25A12-related_disorder|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_39": 5,
    "Developmental_and_epileptic_encephalopathy|_39|not_provided": 4,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia": 118,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 40,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 80,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 88,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 15,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|Inborn_genetic_diseases": 7,
    "Epidermolysis_bullosa|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|ITGA6-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|ITGA6-related_disorder|not_provided": 2,
    "not_provided|ITGA6-related_disorder": 5,
    "not_provided|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 14,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|not_provided": 3,
    "ITGA6-related_disorder": 4,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 4,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 3,
    "ITGA6-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "ITGA6-related_disorder|not_provided|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 6,
    "ITGA6-related_disorder|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|ITGA6-related_disorder|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 1,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_6|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 3,
    "MAP3K20-related_disorder": 5,
    "Myopathy|_centronuclear|_6|_with_fiber-type_disproportion|Split-foot_malformation-mesoaxial_polydactyly_syndrome": 1,
    "not_provided|MAP3K20-related_disorder": 3,
    "not_provided|Split-foot_malformation-mesoaxial_polydactyly_syndrome|Myopathy|_centronuclear|_6|_with_fiber-type_disproportion": 1,
    "Centronuclear_myopathy|Myopathy|_centronuclear|_6|_with_fiber-type_disproportion": 1,
    "Myopathy|_centronuclear|_6|_with_fiber-type_disproportion|not_provided": 1,
    "Split-foot_malformation-mesoaxial_polydactyly_syndrome|Myopathy|_centronuclear|_6|_with_fiber-type_disproportion|not_provided": 2,
    "Split-foot_malformation-mesoaxial_polydactyly_syndrome|not_provided": 1,
    "Split-foot_malformation-mesoaxial_polydactyly_syndrome": 2,
    "Split-foot_malformation-mesoaxial_polydactyly_syndrome|Split_hand-foot_malformation_1": 1,
    "MAP3K20-related_disorder|not_provided": 2,
    "Myopathy|_centronuclear|_6|_with_fiber-type_disproportion|not_provided|Split-foot_malformation-mesoaxial_polydactyly_syndrome": 1,
    "Myopathy|_centronuclear|_6|_with_fiber-type_disproportion|Split-foot_malformation-mesoaxial_polydactyly_syndrome|not_provided": 1,
    "Myopathy|_centronuclear|_6|_with_fiber-type_disproportion|MAP3K20-related_disorder|Split-foot_malformation-mesoaxial_polydactyly_syndrome|not_provided": 1,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_3": 2,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_3": 5,
    "not_provided|CDCA7-related_disorder": 2,
    "CDCA7-related_disorder": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_3|not_provided": 6,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_3|not_provided|CDCA7-related_disorder": 1,
    "CDCA7-related_disorder|not_provided": 3,
    "Abnormal_caudate_nucleus_morphology|Epileptic_encephalopathy|Intellectual_disability": 1,
    "SP9-associated_disorder|Intellectual_disability|EEG_abnormality|Epileptic_encephalopathy|Hypotonia": 1,
    "Convulsive_status_epilepticus|Intellectual_disability|Hypotonia|Epileptic_spasm|Autistic_behavior|EEG_abnormality": 1,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_specified": 4,
    "Wiskott-Aldrich_syndrome_2": 225,
    "not_provided|not_specified|Wiskott-Aldrich_syndrome_2": 1,
    "Wiskott-Aldrich_syndrome_2|not_provided": 9,
    "not_provided|Wiskott-Aldrich_syndrome_2": 9,
    "WIPF1-related_disorder|Wiskott-Aldrich_syndrome_2": 3,
    "Inborn_genetic_diseases|Wiskott-Aldrich_syndrome_2": 16,
    "Wiskott-Aldrich_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Wiskott-Aldrich_syndrome_2|Inborn_genetic_diseases": 8,
    "Wiskott-Aldrich_syndrome_2|WIPF1-related_disorder": 3,
    "WIPF1-related_disorder|not_provided|Wiskott-Aldrich_syndrome_2": 1,
    "not_provided|Inborn_genetic_diseases|Wiskott-Aldrich_syndrome_2": 1,
    "Wiskott-Aldrich_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Wiskott-Aldrich_syndrome_2|WIPF1-related_disorder": 1,
    "not_provided|Wiskott-Aldrich_syndrome_2|not_specified": 1,
    "not_provided|Wiskott-Aldrich_syndrome_2|WIPF1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Wiskott-Aldrich_syndrome_2|WIPF1-related_disorder": 1,
    "Wiskott-Aldrich_syndrome_2|WIPF1-related_disorder|not_provided": 1,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome|not_provided": 5,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome": 32,
    "Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 35,
    "Congenital_myasthenic_syndrome|not_provided|Lethal_multiple_pterygium_syndrome": 3,
    "Lethal_multiple_pterygium_syndrome": 580,
    "Lethal_multiple_pterygium_syndrome|not_provided": 25,
    "not_provided|Lethal_multiple_pterygium_syndrome": 44,
    "Centronuclear_myopathy|not_provided|Lethal_multiple_pterygium_syndrome|Autism|Seizure": 1,
    "not_specified|Lethal_multiple_pterygium_syndrome": 2,
    "CHRNA1-related_disorder": 7,
    "Congenital_myasthenic_syndrome_1A": 9,
    "Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|CHRNA1-related_disorder|Congenital_myasthenic_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases|Congenital_myasthenic_syndrome": 1,
    "CHRNA1-related_disorder|Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided": 1,
    "Lethal_multiple_pterygium_syndrome|not_specified": 5,
    "not_provided|Lethal_multiple_pterygium_syndrome|not_specified": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases": 25,
    "Congenital_myasthenic_syndrome_1A|not_provided|Lethal_multiple_pterygium_syndrome": 2,
    "Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome": 19,
    "Lethal_multiple_pterygium_syndrome|not_provided|Inborn_genetic_diseases": 9,
    "Congenital_myasthenic_syndrome|not_specified|not_provided|Lethal_multiple_pterygium_syndrome": 8,
    "Inborn_genetic_diseases|not_provided|Lethal_multiple_pterygium_syndrome": 6,
    "Lethal_multiple_pterygium_syndrome|not_provided|CHRNA1-related_disorder": 1,
    "Myasthenic_syndrome|_congenital|_1B|_fast-channel|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_1A|not_provided": 1,
    "CHRNA1-related_disorder|Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 3,
    "not_provided|Myasthenic_syndrome|_congenital|_1B|_fast-channel|Lethal_multiple_pterygium_syndrome": 1,
    "CHRNA1-Related_Congenital_Myasthenic_Syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|CHRNA1-related_disorder": 4,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "CHRNA1-related_disorder|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|Myasthenic_syndrome|_congenital|_1B|_fast-channel|Congenital_myasthenic_syndrome_1A": 1,
    "Myasthenic_syndrome|_congenital|_1B|_fast-channel": 6,
    "not_provided|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome": 5,
    "Congenital_myasthenic_syndrome_1A|Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|Myasthenic_syndrome|_congenital|_1B|_fast-channel": 1,
    "Lethal_multiple_pterygium_syndrome|not_provided|Congenital_myasthenic_syndrome": 1,
    "Autosomal_recessive_multiple_pterygium_syndrome|Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Lethal_multiple_pterygium_syndrome": 1,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|not_provided|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Autosomal_recessive_multiple_pterygium_syndrome|not_provided": 1,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_1A|not_provided": 1,
    "Lethal_multiple_pterygium_syndrome|Myasthenic_syndrome|_congenital|_1B|_fast-channel": 3,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_1A": 3,
    "not_provided|Lethal_multiple_pterygium_syndrome|Slow-Channel_Congenital_Myasthenia_Syndrome": 1,
    "Slow-Channel_Congenital_Myasthenia_Syndrome": 2,
    "Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "CHRNA1-related_disorder|Lethal_multiple_pterygium_syndrome": 2,
    "Congenital_myasthenic_syndrome|not_specified|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "not_specified|Congenital_myasthenic_syndrome|not_provided|Lethal_multiple_pterygium_syndrome": 1,
    "Congenital_myasthenic_syndrome_1A|Lethal_multiple_pterygium_syndrome|Myasthenic_syndrome|_congenital|_1B|_fast-channel|not_provided": 1,
    "Myasthenic_syndrome|_congenital|_1B|_fast-channel|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_1A|Congenital_myopathy|not_provided": 1,
    "Lethal_multiple_pterygium_syndrome|See_cases": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|Epilepsy|Seizure": 1,
    "Myasthenic_syndrome|_congenital|_1B|_fast-channel|Lethal_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_1A": 1,
    "Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome|not_provided|Juvenile_myoclonic_epilepsy": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases": 5,
    "not_specified|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|Myasthenic_syndrome|_congenital|_1B|_fast-channel|CHRNA1-related_disorder": 1,
    "Congenital_myasthenic_syndrome_1A|not_specified|not_provided|Myasthenic_syndrome|_congenital|_1B|_fast-channel|Lethal_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Myasthenic_syndrome|_congenital|_1B|_fast-channel|Congenital_myasthenic_syndrome_1A": 1,
    "Congenital_myasthenic_syndrome_1A|Congenital_Myasthenic_Syndrome|_Dominant/Recessive|not_specified|not_provided|Myasthenic_syndrome|_congenital|_1B|_fast-channel|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Hydrops_fetalis|Fetal_ascites|Pleural_effusion|Lethal_multiple_pterygium_syndrome": 1,
    "Myasthenic_syndrome|_congenital|_1B|_fast-channel|not_provided|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_1A": 1,
    "Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "not_specified|not_provided|CHRNA1-related_disorder": 1,
    "not_specified|not_provided|Lethal_multiple_pterygium_syndrome": 4,
    "Duane_retraction_syndrome_2": 48,
    "Duane_retraction_syndrome_2|not_provided": 3,
    "Duane_syndrome_type_1": 1,
    "CHN1-related_disorder": 1,
    "Inborn_genetic_diseases|Duane_retraction_syndrome_2": 2,
    "not_provided|CHN1-related_disorder": 2,
    "not_provided|Duane_retraction_syndrome_2": 7,
    "Duane_retraction_syndrome_2|Inborn_genetic_diseases": 2,
    "Duane_retraction_syndrome|not_provided": 2,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|ATP5G3-associated_disorder": 1,
    "LNPK-related_disorder": 11,
    "Neurodevelopmental_disorder_with_epilepsy_and_hypoplasia_of_the_corpus_callosum": 16,
    "LNPK-related_disorder|not_provided": 1,
    "not_provided|LNPK-related_disorder": 1,
    "Synpolydactyly_type_1": 14,
    "EVX2-related_disorder": 4,
    "Brachydactyly_type_D|Brachydactyly_type_E1|not_provided|Synpolydactyly_type_1": 1,
    "HOXD13-related_disorder": 7,
    "VATER_association": 6,
    "Brachydactyly-syndactyly_syndrome|not_provided": 1,
    "not_provided|HOXD13-related_disorder": 4,
    "Brachydactyly_type_D|Brachydactyly-syndactyly_syndrome|Brachydactyly_type_E1|Syndactyly_type_5|Synpolydactyly_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Syndactyly_type_5|Brachydactyly-syndactyly_syndrome|Brachydactyly_type_D|Synpolydactyly_type_1|Brachydactyly_type_E1|Inborn_genetic_diseases|not_provided": 1,
    "HOXD13-related_disorder|not_provided": 2,
    "Brachydactyly-syndactyly_syndrome": 1,
    "Skeletal_dysplasia|not_provided": 3,
    "Brachydactyly_type_D|Syndactyly_type_5|Brachydactyly-syndactyly_syndrome|Synpolydactyly_type_1|Brachydactyly_type_E1|not_provided": 1,
    "not_provided|Brachydactyly-syndactyly_syndrome": 1,
    "not_provided|not_specified|Synpolydactyly_type_1|Brachydactyly_type_E1|Brachydactyly_type_D|Syndactyly_type_5": 1,
    "Synpolydactyly_type_1|not_provided": 1,
    "Syndactyly_type_5|Synpolydactyly_type_1": 1,
    "Brachydactyly-syndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Brachydactyly_type_E1|Syndactyly_type_5|Brachydactyly_type_D|Brachydactyly-syndactyly_syndrome|Synpolydactyly_type_1|HOXD13-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|HOXD13-related_disorder": 1,
    "Inborn_genetic_diseases|Brachydactyly_type_E1|Synpolydactyly_type_1|Syndactyly_type_5|Brachydactyly-syndactyly_syndrome|Brachydactyly_type_D": 1,
    "HOXD13-related_disorder|not_specified|not_provided": 1,
    "not_provided|HOXD13-related_disorder|not_specified": 1,
    "Brachydactyly_type_E1|Brachydactyly_type_D|Syndactyly_type_5|Synpolydactyly_type_1": 1,
    "Synpolydactyly|Brachydactyly-syndactyly_syndrome|Brachydactyly_type_D|Syndactyly_type_5|Synpolydactyly_type_1|Brachydactyly_type_E1|Male_infertility|Oligospermia|Syndactyly|Mesoaxial_hand_polydactyly|Penile_hypospadias|Polydactyly|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Synpolydactyly_type_1|Brachydactyly_type_E1": 1,
    "Abnormal_finger_morphology|not_provided": 1,
    "Brachydactyly_type_D|Brachydactyly_type_E|not_provided|Inborn_genetic_diseases": 1,
    "Brachydactyly_type_E1|Synpolydactyly_type_1|Brachydactyly-syndactyly_syndrome|Brachydactyly_type_D|Syndactyly_type_5": 1,
    "Brachydactyly_type_E|Brachydactyly_type_D": 1,
    "Brachydactyly-syndactyly-oligodactyly_syndrome": 1,
    "Syndactyly_type_5": 1,
    "Brachydactyly_type_E1|Synpolydactyly_type_1|Brachydactyly-syndactyly_syndrome|Syndactyly_type_5|Brachydactyly_type_D": 1,
    "HOXD12-related_disorder": 1,
    "not_specified|HOXD12-related_disorder": 1,
    "Congenital_vertical_talus": 22,
    "HOXD10-related_disorder": 2,
    "not_specified|Congenital_vertical_talus": 1,
    "not_provided|not_specified|Congenital_vertical_talus": 1,
    "Congenital_vertical_talus|not_specified": 2,
    "HOXD10-related_disorder|not_provided": 1,
    "Congenital_vertical_talus|not_provided|not_specified": 1,
    "Congenital_vertical_talus|HOXD10-related_disorder": 1,
    "Congenital_vertical_talus|not_provided": 8,
    "not_provided|Congenital_vertical_talus": 9,
    "HOXD9-related_disorder": 3,
    "HOXD8-related_disorder": 1,
    "Leukemia|_acute_lymphoblastic|_susceptibility_to": 1,
    "Progeroid_mandibuloacral_dysplasia|Mandibuloacral_dysplasia_progeroid_syndrome": 4,
    "Mandibuloacral_dysplasia_progeroid_syndrome": 1,
    "Abnormality_of_skin_pigmentation|Facial_shape_deformation|Dental_crowding|Progeroid_facial_appearance|Micrognathia|Acroosteolysis_of_distal_phalanges_(feet)|Postnatal_growth_retardation|Hypertensive_disorder|Abnormal_mandible_morphology|Abnormality_of_body_height|Mandibuloacral_dysplasia_progeroid_syndrome": 1,
    "NFE2L2-related_disorder": 3,
    "not_provided|not_specified|NFE2L2-related_disorder": 1,
    "Immunodeficiency|_developmental_delay|_and_hypohomocysteinemia": 7,
    "not_provided|NFE2L2-related_disorder": 4,
    "Immunodeficiency|_developmental_delay|_and_hypohomocysteinemia|not_provided": 4,
    "NFE2L2-related_disorder|not_provided": 6,
    "not_provided|Immunodeficiency|_developmental_delay|_and_hypohomocysteinemia|not_specified": 1,
    "not_provided|Immunodeficiency|_developmental_delay|_and_hypohomocysteinemia": 3,
    "NFE2L2-related_disorder|not_provided|not_specified": 1,
    "NFE2L2-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|NFE2L2-related_disorder": 1,
    "Immunodeficiency|_developmental_delay|_and_hypohomocysteinemia|Colorectal_cancer": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_3": 139,
    "not_provided|AGPS-related_disorder": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_3|not_provided": 26,
    "Rhizomelic_chondrodysplasia_punctata_type_3|Rhizomelic_chondrodysplasia_punctata": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_3|not_provided|not_specified": 4,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_3": 14,
    "not_provided|Rhizomelic_chondrodysplasia_punctata": 7,
    "Rhizomelic_chondrodysplasia_punctata_type_3|Inborn_genetic_diseases|not_provided": 2,
    "Rhizomelic_chondrodysplasia_punctata_type_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_3": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_3|not_specified|not_provided|Rhizomelic_chondrodysplasia_punctata": 2,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_3|Rhizomelic_chondrodysplasia_punctata": 1,
    "AGPS-related_disorder|not_provided": 2,
    "Rhizomelic_chondrodysplasia_punctata_type_3|not_provided|Rhizomelic_chondrodysplasia_punctata|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Rhizomelic_chondrodysplasia_punctata_type_3|not_provided|AGPS-related_disorder": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_3|not_specified|not_provided": 2,
    "not_provided|AGPS-related_disorder|Rhizomelic_chondrodysplasia_punctata_type_3": 1,
    "AGPS-related_disorder|not_provided|Rhizomelic_chondrodysplasia_punctata": 1,
    "not_provided|Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_3": 1,
    "not_provided|Rhizomelic_chondrodysplasia_punctata|Rhizomelic_chondrodysplasia_punctata_type_3": 1,
    "not_specified|not_provided|Rhizomelic_chondrodysplasia_punctata_type_3": 2,
    "Rhizomelic_chondrodysplasia_punctata|AGPS-related_disorder|not_provided": 1,
    "IFT70B-related_disorder|not_specified|not_provided": 1,
    "IFT70B-related_disorder|not_provided": 1,
    "IFT70B-related_disorder": 2,
    "Synpolydactyly": 1,
    "PDE11A-related_disorder": 16,
    "Pigmented_nodular_adrenocortical_disease|_primary|_2|not_provided": 10,
    "Pigmented_nodular_adrenocortical_disease|_primary|_2|not_specified": 2,
    "not_provided|PDE11A-related_disorder": 5,
    "PDE11A-related_disorder|not_provided|Pigmented_nodular_adrenocortical_disease|_primary|_2": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_2": 23,
    "PDE11A-related_disorder|not_provided": 4,
    "Pigmented_nodular_adrenocortical_disease|_primary|_2|PDE11A-related_disorder": 1,
    "not_provided|PDE11A-related_disorder|Pigmented_nodular_adrenocortical_disease|_primary|_2": 1,
    "not_provided|Pigmented_nodular_adrenocortical_disease|_primary|_2": 4,
    "PDE11A-related_disorder|Pigmented_nodular_adrenocortical_disease|_primary|_2|not_provided": 2,
    "not_provided|Pigmented_nodular_adrenocortical_disease|_primary|_2|See_cases": 1,
    "PDE11A-related_disorder|not_specified|Bardet-Biedl_syndrome_16|not_provided|Pigmented_nodular_adrenocortical_disease|_primary|_2": 1,
    "not_provided|Dystonia_16": 17,
    "Dystonia_16": 94,
    "Dystonia_16|not_provided": 10,
    "Dystonia_16|Inborn_genetic_diseases": 1,
    "PRKRA-related_disorder": 2,
    "not_provided|Dystonia_16|not_specified": 1,
    "PRKRA-related_disorder|not_provided|Dystonia_16": 1,
    "Dystonia_16|Dystonic_disorder|not_provided": 2,
    "Dystonic_disorder|not_provided|Dystonia_16": 1,
    "Inborn_genetic_diseases|Dystonia_16": 1,
    "Hearing_loss|_autosomal_recessive|Dystonia_16|Dystonic_disorder|not_provided": 1,
    "not_provided|Dystonia_16|Dystonic_disorder|not_specified|Hearing_loss|_autosomal_recessive": 1,
    "Hearing_loss|_autosomal_recessive|Dystonic_disorder|not_provided|not_specified|Dystonia_16": 1,
    "Hearing_loss|_autosomal_recessive|Dystonic_disorder|not_provided|Dystonia_16": 1,
    "not_provided|Dystonia_16|Dystonic_disorder": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_59": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_59": 31,
    "not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_59": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_59|not_provided": 6,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_59": 2,
    "not_provided|Dystonic_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_59": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_59": 8,
    "not_provided|PJVK-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_59|not_specified": 1,
    "not_provided|PJVK-related_disorder": 2,
    "Deafness|Hearing_loss|_autosomal_recessive": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_59|not_specified|not_provided": 2,
    "PJVK-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_59|not_provided": 1,
    "PJVK-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_59": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_59|PJVK-related_disorder|not_provided|not_specified": 1,
    "not_provided|Deafness|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_59": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_59|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_59|Rare_genetic_deafness|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_59|Ear_malformation": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_59": 3,
    "Deafness": 9,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_59|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_59": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_59|not_provided": 1,
    "TTN-related_disorder": 238,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 5,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 7,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 6,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 8,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 4,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 12,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 3,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 6785,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 6626,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 19,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 410,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 389,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 223,
    "Tibial_muscular_dystrophy": 24,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 194,
    "not_specified|Tibial_muscular_dystrophy": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_titinopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 419,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 12,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 570,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 50,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 580,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 10,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_familial_dilated_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 51,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 46,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Autosomal_recessive_centronuclear_myopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 6,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 101,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified": 10,
    "not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 10,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 20,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 23,
    "not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 66,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 95,
    "TTN-related_disorder|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "Cardiovascular_phenotype|TTN-related_myopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Neuromuscular_disease|not_provided|Limb-girdle_muscle_weakness|Limb-girdle_muscle_atrophy|Muscular_dystrophy|Limb-girdle_muscular_dystrophy|Proximal_lower_limb_amyotrophy|Decreased_patellar_reflex|Waddling_gait|Lower_limb_muscle_weakness|Rimmed_vacuoles|Myopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 45,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 24,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 36,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 29,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided": 10,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided": 17,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 4,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 200,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Centronuclear_myopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Neuromuscular_disease|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype": 3,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy": 38,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 31,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 6,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype": 51,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Left_ventricular_noncompaction_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 58,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 8,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 3,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 259,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 383,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 5,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 7,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 40,
    "Tip-toe_gait|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 12,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype": 21,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G": 420,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 27,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 7,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 119,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 22,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 5,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 2,
    "TTN-related_myopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|TTN-related_myopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 65,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 3,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 9,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 30,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Tip-toe_gait": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 56,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 46,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Tip-toe_gait|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 35,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 23,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Centronuclear_myopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy": 1,
    "not_provided|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified": 19,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 2,
    "not_provided|Dilated_cardiomyopathy_1G": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 4,
    "not_provided|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 12,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|TTN-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 29,
    "TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 52,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder": 4,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 37,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 19,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 8,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 11,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 78,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 7,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 6,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Tip-toe_gait": 3,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 5,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|See_cases|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 19,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 24,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 14,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype": 47,
    "not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 10,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 110,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 8,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|TTN-related_disorder|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 11,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Tip-toe_gait": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Limb-girdle_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 9,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 2,
    "not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 7,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "not_specified|Left_ventricular_noncompaction_2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 13,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy": 10,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 7,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy": 32,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 14,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 10,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 12,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy": 7,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 4,
    "not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 5,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 5,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|TTN-related_myopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 2,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 41,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified": 26,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G": 9,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 20,
    "TTN-related_myopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Ventricular_fibrillation|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder": 10,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 18,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 5,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 4,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 25,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 29,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 33,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "Multiminicore_myopathy": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 2,
    "not_specified|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 6,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 7,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 18,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Primary_familial_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|TTN-related_disorder|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 23,
    "not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 22,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 12,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|TTN-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Primary_dilated_cardiomyopathy|Muscular_dystrophy|Limb-girdle_muscular_dystrophy|Decreased_patellar_reflex|Proximal_lower_limb_amyotrophy|Waddling_gait|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Left_ventricular_noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|not_provided": 8,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified": 7,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 9,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tip-toe_gait": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 7,
    "not_specified|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 12,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|not_provided|TTN-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder": 1,
    "not_provided|Cardiomyopathy|Multiminicore_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|not_provided|Cardiomyopathy": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 3,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 7,
    "not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_specified|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Heart_failure|Primary_dilated_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 69,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 9,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified": 9,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 12,
    "not_specified|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 8,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 6,
    "not_provided|TTN-related_disorder": 26,
    "Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9": 25,
    "not_provided|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Ventricular_tachycardia|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_9": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Supraventricular_tachycardia|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 3,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 24,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 7,
    "not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 14,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified": 5,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 6,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 5,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "TTN-related_myopathy|Atrial_fibrillation|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 10,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "not_specified|TTN-related_disorder|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|TTN-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|not_provided": 17,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 31,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_2|not_specified": 1,
    "Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_2|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|TTN-related_disorder|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|Delayed_speech_and_language_development|Hypotonia|Generalized_hypotonia|Abnormality_of_eye_movement|Abnormal_speech_pattern|Delayed_gross_motor_development": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 11,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 6,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 9,
    "Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 4,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Cardiovascular_phenotype": 6,
    "not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 11,
    "Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|See_cases|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 4,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 3,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 4,
    "Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Titinopathy": 3,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 22,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|TTN-related_myopathy": 1,
    "not_provided|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_specified|not_provided": 1,
    "Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Brugada_syndrome": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 5,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 3,
    "not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 4,
    "Neurodevelopmental_delay|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_titinopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Primary_familial_dilated_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 9,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 10,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Dilated_cardiomyopathy_1S": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Cardiomyopathy|Intellectual_disability": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 19,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_cardiomyopathy": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 11,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 3,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait|Hypertrophic_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 3,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 6,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 40,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 21,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 15,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 15,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Inborn_genetic_diseases|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy": 4,
    "Cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|SUDDEN_INFANT_DEATH_SYNDROME|Primary_dilated_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided": 3,
    "not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 5,
    "Dilated_cardiomyopathy_1G|Centronuclear_myopathy|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 10,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 4,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "TTN-related_disorder|not_specified|not_provided": 19,
    "not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder": 1,
    "not_specified|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 4,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Skeletal_dysplasia|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_myopathy": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 2,
    "Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 7,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 12,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 6,
    "TTN-related_disorder|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified": 6,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Cardiomyopathy": 1,
    "TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 7,
    "not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 6,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Limb-girdle_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 3,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 5,
    "not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Ventricular_fibrillation|Cardiomyopathy|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "not_specified|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|not_provided|not_specified": 7,
    "TTN-related_disorder|not_provided": 39,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Tibial_muscular_dystrophy": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "not_provided|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Ventricular_tachycardia|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 6,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Hereditary_inclusion-body_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Primary_familial_dilated_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 7,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided": 6,
    "not_specified|Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 5,
    "Cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 3,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_myopathy|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|See_cases|not_specified|not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 20,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified": 1,
    "not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Mitral_valve_prolapse": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiovascular_phenotype": 5,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Cardiovascular_phenotype|TTN-related_disorder|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 8,
    "Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 13,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Myopathy": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 5,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 3,
    "Cardiovascular_phenotype|TTN-related_disorder|not_provided|Left_ventricular_hypertrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Limb-girdle_muscular_dystrophy|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|not_specified": 11,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 27,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 7,
    "not_provided|Congenital_titinopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_familial_dilated_cardiomyopathy|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "TTN-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Arthrogryposis_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Primary_dilated_cardiomyopathy|Wolff-Parkinson-White_pattern|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 3,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided": 4,
    "not_provided|Dilated_cardiomyopathy_1S": 4,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 5,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 8,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 5,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided": 1,
    "TTN-related_myopathy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Supraventricular_tachycardia|Hypertrophic_cardiomyopathy|Tip-toe_gait": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Left_ventricular_noncompaction": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 2,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_provided|SUDDEN_INFANT_DEATH_SYNDROME": 3,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Distal_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 3,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "TTN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype": 4,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 3,
    "not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 15,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|TTN-related_disorder|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Limb-girdle_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Cardiovascular_phenotype|EBV-positive_nodal_T-_and_NK-cell_lymphoma|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 19,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype": 9,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 4,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|TTN-related_disorder|Ventricular_fibrillation|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Ventricular_tachycardia|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 2,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|TTN-related_disorder": 5,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Delayed_speech_and_language_development|Hypotonia|Short_stature|Failure_to_thrive|Abnormal_speech_pattern|Abnormality_of_the_immune_system|Generalized_muscle_weakness": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 3,
    "Cardiomyopathy|not_provided|not_specified|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|TTN-related_disorder|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy": 5,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_myopathy|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Abnormality_of_neuronal_migration|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified|TTN-related_disorder|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|TTN-related_disorder": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 2,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|not_provided": 3,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Family_history_of_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 13,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|not_specified|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "TTN-related_disorder|Cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy": 9,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 7,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Atrial_fibrillation|Ventricular_tachycardia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiovascular_phenotype": 6,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|not_provided|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_myopathy": 10,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 2,
    "not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Tip-toe_gait|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 6,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|TTN-related_disorder|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 2,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tip-toe_gait": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_titinopathy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 15,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Arthrogryposis_syndrome|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided": 5,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 3,
    "Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|not_specified|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Inborn_genetic_diseases|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 2,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Cardiomyopathy|TTN-related_myopathy|not_specified|not_provided": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Ventricular_fibrillation": 1,
    "Primary_familial_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 3,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy": 5,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Congestive_heart_failure": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "not_provided|TTN-related_disorder|not_specified": 9,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Primary_familial_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Heart_failure": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy": 9,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 3,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "not_provided|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiovascular_phenotype|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 8,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Brugada_syndrome|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_titinopathy": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_myopathy|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|TTN-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Amyloidosis|_hereditary_systemic_1|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|TTN-related_disorder|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tip-toe_gait|not_specified|not_provided": 1,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 4,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy": 5,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|not_provided": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Third_degree_atrioventricular_block|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|Myopathy|Cardiovascular_phenotype|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 2,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 4,
    "not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "TTN-related_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_2": 1,
    "not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_familial_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Left_ventricular_hypertrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy": 7,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 16,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Tibial_muscular_dystrophy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 12,
    "not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 2,
    "Primary_dilated_cardiomyopathy|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 3,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_myopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_specified": 2,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|not_provided": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_9": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "TTN-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Premature_ventricular_contraction|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 4,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|not_provided|not_specified|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided|TTN-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|TTN-related_disorder|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Cardiomyopathy|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 4,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 4,
    "not_specified|Dilated_cardiomyopathy_1G": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 4,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy": 57,
    "not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 5,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Tip-toe_gait": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Sudden_cardiac_arrest": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|TTN-related_disorder": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 2,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tip-toe_gait": 1,
    "Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Left_ventricular_noncompaction_2": 2,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Inborn_genetic_diseases|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|TTN-related_disorder|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 4,
    "Cardiomyopathy|TTN-related_disorder": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Hereditary_skeletal_muscle_disorder": 3,
    "not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|not_specified|TTN-related_disorder|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 9,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 3,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|TTN-related_disorder|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|Ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 5,
    "not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 2,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Cardiovascular_phenotype|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 1,
    "not_provided|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiovascular_phenotype|Inborn_genetic_diseases": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_familial_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Myopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 3,
    "not_provided|Tibial_muscular_dystrophy|Atrial_fibrillation|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|See_cases": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided": 6,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "TTN-related_disorder|Cardiomyopathy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 3,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiomyopathy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Cardiovascular_phenotype|TTN-related_disorder|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 2,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_myopathy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9": 2,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Centronuclear_myopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Distal_myopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Restrictive_cardiomyopathy": 7,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|not_provided": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Premature_ventricular_contraction": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Rare_genetic_intellectual_disability|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified": 5,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "Interstitial_cardiac_fibrosis": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 5,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder": 2,
    "Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "See_cases|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Brugada_syndrome|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9": 1,
    "Hypertrophic_cardiomyopathy|Ventricular_tachycardia|Familial_dilated_cardiomyopathy_and_peripheral_neuropathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|TTN-related_disorder": 2,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "TTN-related_myopathy|Cardiovascular_phenotype|Atrial_fibrillation|Hypertrophic_cardiomyopathy|Brugada_syndrome|Congestive_heart_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "TTN-related_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 3,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tip-toe_gait": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Bilateral_talipes_equinovarus|Restrictive_ventilatory_defect|Spinal_rigidity|Areflexia_of_lower_limbs|Thoracic_kyphoscoliosis": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|Tip-toe_gait": 6,
    "not_provided|Cardiomyopathy|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Restrictive_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Familial_restrictive_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 3,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|TTN-related_disorder": 5,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|not_specified|TTN-related_disorder": 3,
    "Cardiovascular_phenotype|not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 3,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Centronuclear_myopathy|Feingold_syndrome_type_1|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 3,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1A|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 2,
    "not_specified|Cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Brugada_syndrome|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 4,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided": 1,
    "TTN-related_disorder|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tip-toe_gait": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Sudden_cardiac_arrest|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Tip-toe_gait|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 10,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 6,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Primary_dilated_cardiomyopathy": 3,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9": 6,
    "Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 4,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Cardiomyopathy|TTN-related_disorder|Primary_dilated_cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|TTN-related_disorder": 2,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|TTN-related_disorder|Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|TTN-related_disorder": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|not_specified": 3,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|not_provided|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|TTN-related_disorder": 1,
    "not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Hypertrophic_cardiomyopathy|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided": 3,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 3,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Atrial_fibrillation": 7,
    "Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy": 13,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Congenital_myopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Tip-toe_gait": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_specified|Cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 4,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Long_QT_syndrome|Heart_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Congestive_heart_failure|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Distal_myopathy|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype": 2,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 6,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1S|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Conduction_disorder_of_the_heart": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|TTN-related_disorder|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|TTN-related_disorder": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Skeletal_dysplasia": 19,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 4,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|TTN-related_disorder|Tip-toe_gait|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 4,
    "not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy": 3,
    "TTN-related_disorder|not_provided|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|not_provided": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|See_cases|Long_QT_syndrome|Heart_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G": 2,
    "Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 19,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|TTN-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified": 1,
    "not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Arthrogryposis_syndrome|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|TTN-related_disorder|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 9,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|See_cases": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Long_QT_syndrome|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "TTN-related_disorder|not_specified": 13,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified": 1,
    "Ventricular_fibrillation|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "Premature_ventricular_contraction": 1,
    "Tibial_muscular_dystrophy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_2|not_specified|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_2|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|not_specified|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Ventricular_tachycardia": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Desmin-related_myofibrillar_myopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiomyopathy|not_specified|Ventricular_fibrillation|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|not_specified": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Hypertrophic_cardiomyopathy_9": 4,
    "Cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|TTN-related_disorder|not_provided|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|not_specified": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|TTN-related_disorder|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Primary_familial_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Tibial_muscular_dystrophy": 3,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 2,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 2,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|TTN-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tip-toe_gait|not_provided": 4,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 4,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Ventricular_tachycardia": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|TTN-related_myopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_myopathy|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Primary_dilated_cardiomyopathy": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|TTN-related_disorder": 7,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Skeletal_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Tip-toe_gait|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "Cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "not_specified|Tibial_muscular_dystrophy|Cardiovascular_phenotype|TTN-related_disorder|Cardiomyopathy|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 3,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|not_provided|Cardiomyopathy": 2,
    "TTN-related_disorder|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 2,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Centronuclear_myopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|TTN-related_disorder|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Dilated_cardiomyopathy_1A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "Ventricular_tachycardia": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tip-toe_gait": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Reduced_left_ventricular_ejection_fraction|Noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Tip-toe_gait": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified": 1,
    "not_provided|TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 3,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "not_specified|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified": 1,
    "Third_degree_atrioventricular_block": 4,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 6,
    "not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 5,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Limb-girdle_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|TTN-related_disorder|not_provided": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1A": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Cardiomyopathy|Noncompaction_cardiomyopathy|Low-output_congestive_heart_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy|Ventricular_tachycardia|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|TTN-related_myopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Non-compaction_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Primary_dilated_cardiomyopathy|Atrial_fibrillation|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Limb-girdle_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Limb-girdle_muscular_dystrophy|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 10,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Tibial_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|TTN-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|TTN-related_disorder|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 2,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|TTN-related_disorder|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 3,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Diastolic_dysfunction": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|not_provided|not_specified": 4,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction_2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 2,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "not_specified|Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiomyopathy|not_specified|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 15,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|not_provided|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Congenital_myopathy|not_specified|not_provided": 1,
    "not_provided|TTN-related_myopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Congenital_titinopathy": 1,
    "not_provided|TTN-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Autosomal_recessive_titinopathy|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Primary_dilated_cardiomyopathy": 5,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 2,
    "TTN-related_disorder|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Atrial_fibrillation|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified": 2,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "autosomal_dominant_dilated_cardiomyopathy|autosomal_dominant_myopathies|autosomal_recessive_myopathies|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 3,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|Congenital_long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Centronuclear_myopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified": 1,
    "not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|TTN-related_disorder|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TNN-related_disorder|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Myopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 2,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "TTN-related_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|not_provided": 1,
    "Primary_familial_dilated_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_myopathy|not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Left_ventricular_hypertrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|not_provided": 4,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Autosomal_recessive_titinopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 3,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Supraventricular_tachycardia|Cardiomyopathy|TTN-related_disorder|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 4,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tip-toe_gait": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|TTN-related_disorder|Cardiomyopathy": 1,
    "TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|TTN-related_disorder|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 44,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_myopathy|CAP-congenital_myopathy_with_arthrogryposis_multiplex_congenita_without_heart_involvement|not_provided": 1,
    "TTN-related_disorder|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_titinopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_2": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 3,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Primary_dilated_cardiomyopathy|TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_provided|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 10,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 1,
    "Autosomal_recessive_titinopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|TTN-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Congenital_myopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Primary_familial_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "TTN-related_disorder|Autosomal_recessive_titinopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Primary_familial_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|TTN-related_myopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "not_specified|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|See_cases": 1,
    "not_provided|TTN-related_disorder|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Centronuclear_myopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_myopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 3,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Myopathy|_centronuclear|_2|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified": 1,
    "not_specified|Limb-girdle_muscular_dystrophy|Cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 2,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_familial_dilated_cardiomyopathy|not_specified|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|See_cases|Tibial_muscular_dystrophy|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Congenital_myopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|TTN-related_disorder|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Centronuclear_myopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Congenital_myopathy": 1,
    "TTN-related_disorder|not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|not_specified|TTN-related_disorder": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|Tip-toe_gait|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Heart_failure|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Brugada_syndrome|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified|Hypertrophic_cardiomyopathy_9": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy": 2,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Autosomal_recessive_titinopathy": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "not_specified|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Brugada_syndrome|Supraventricular_tachycardia|Ventricular_tachycardia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "not_specified|Abnormality_of_neuronal_migration|Hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy": 500,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 5,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided|TTN-related_disorder": 1,
    "TTN-related_disorder|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Tip-toe_gait": 1,
    "not_specified|not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified": 2,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_titinopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy": 5,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 3,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 1,
    "TTN-related_disorder|Cardiomyopathy|Long_QT_syndrome|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tip-toe_gait|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_myopathy|not_specified|not_provided": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Dilated_Cardiomyopathy|_Dominant|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Limb-girdle_muscular_dystrophy|_recessive|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified": 1,
    "TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Restrictive_ventilatory_defect|Bilateral_talipes_equinovarus|Areflexia_of_lower_limbs|Thoracic_kyphoscoliosis|Spinal_rigidity": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Delayed_speech_and_language_development|Hypotonia|Generalized_hypotonia|Abnormality_of_eye_movement|Abnormal_speech_pattern|Delayed_gross_motor_development": 1,
    "not_specified|Primary_dilated_cardiomyopathy|not_provided|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy": 1,
    "Congenital_titinopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_titinopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myocarditis|Primary_dilated_cardiomyopathy|not_provided": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Sudden_cardiac_death|Cardiac_arrest": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Supraventricular_tachycardia": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 6,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 3,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 2,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_myopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Dilated_cardiomyopathy_1G|not_specified|not_provided|TTN-related_disorder|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Left_ventricular_hypertrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy|not_provided": 1,
    "TTN-related_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|TTN-related_disorder|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tip-toe_gait": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Tibial_muscular_dystrophy|TTN-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|not_specified": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided|Hypertrophic_cardiomyopathy|TTN-related_disorder": 1,
    "Distal_myopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Limb-girdle_muscular_dystrophy|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Ventricular_tachycardia|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|not_specified": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|TTN-related_disorder|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tip-toe_gait": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Familial_restrictive_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tip-toe_gait": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tip-toe_gait|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|TTN-related_myopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Long_QT_syndrome|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|not_specified": 1,
    "not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Congestive_heart_failure": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 2,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_provided|TTN-related_disorder|not_specified": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "Autosomal_recessive_titinopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified": 1,
    "Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|TTN-related_disorder": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Congenital_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder": 1,
    "not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Centronuclear_myopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|TTN-related_disorder|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Skeletal_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tip-toe_gait": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Noncompaction_cardiomyopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|not_provided|Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Tip-toe_gait|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Tibial_muscular_dystrophy|Distal_myopathy|not_provided|TTN-related_disorder|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Limb-girdle_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Cardiomyopathy|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 2,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy|Atrial_fibrillation|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Long_QT_syndrome": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "not_provided|TTN-related_disorder|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiomyopathy": 1,
    "Cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 1,
    "TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|TTN-related_disorder|Tibial_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|TTN-related_disorder|not_specified|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Autosomal_recessive_titinopathy|not_provided": 1,
    "TTN-related_disorder|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tip-toe_gait": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Left_ventricular_noncompaction_cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Brugada_syndrome|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "TTN-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "TTN-related_disorder|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Heart_failure": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tip-toe_gait": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiovascular_phenotype|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "TTN-related_disorder|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|TTN-related_disorder": 1,
    "Tibial_muscular_dystrophy|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Congenital_titinopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Orofacial_cleft_1|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_titinopathy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Hereditary_skeletal_muscle_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Congenital_myopathy|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_myopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Neuromuscular_disease": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|not_specified": 1,
    "TTN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Supraventricular_tachycardia|Tip-toe_gait": 1,
    "Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|Long_QT_syndrome|not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "TTN-related_disorder|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy|Heart_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|TTN-related_disorder|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_provided|not_specified": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Distal_myopathy|not_specified|not_provided": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Long_QT_syndrome|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy": 1,
    "TTN-related_disorder|not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_specified|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Autosomal_recessive_centronuclear_myopathy|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|not_provided|See_cases": 5,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "not_provided|not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "See_cases|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder": 1,
    "Arthrogryposis_syndrome": 4,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|TTN-related_disorder|not_provided": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 1,
    "Long_QT_syndrome|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided|not_specified|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy": 1,
    "Right_ventricular_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|TTN-related_disorder": 1,
    "Cardiomyopathy|TTN-related_disorder|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|See_cases": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Supraventricular_tachycardia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|TTN-related_disorder|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Cardiomyopathy|not_specified|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|TTN-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|TTN-related_disorder|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Muscular_dystrophy|EMG_abnormality|Fatty_replacement_of_skeletal_muscle|Gait_disturbance": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Rare_genetic_intellectual_disability": 4,
    "not_specified|not_provided|TTN-related_disorder": 4,
    "TTN-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|TTN-related_disorder|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|TTN-related_disorder|not_specified": 1,
    "not_specified|not_provided|Limb-girdle_muscular_dystrophy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Primary_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Syncope|not_specified|not_provided|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|TTN-related_disorder|not_provided|not_specified": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided": 2,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|not_specified|TTN-related_disorder": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Distal_myopathy": 9,
    "Motor_delay|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|not_provided": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|TTN-related_disorder": 1,
    "not_specified|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided|not_specified": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder": 1,
    "TTN-related_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "not_provided|TTN-related_myopathy|Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|TTN-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|TTN-related_myopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|not_specified|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy": 19,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_specified|TTN-related_disorder|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|TTN-related_disorder|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|TTN-related_disorder|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Atrial_fibrillation|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|TTN-related_disorder": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_titinopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|not_provided|TTN-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Ventricular_tachycardia|Congestive_heart_failure|Atrial_fibrillation|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified": 1,
    "not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 2,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Abnormality_of_neuronal_migration|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Primary_dilated_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1G|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided": 2,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|not_provided|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|TTN-related_disorder": 1,
    "Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Sudden_cardiac_arrest": 1,
    "not_provided|Dilated_cardiomyopathy_1G|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Primary_dilated_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|not_provided|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Ventricular_tachycardia": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy|not_provided": 1,
    "not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tip-toe_gait|not_provided|TTN-related_disorder|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided": 1,
    "TTN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Tip-toe_gait": 1,
    "Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|not_specified|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiomyopathy|TTN-related_disorder|not_provided|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|Systolic_heart_failure|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiovascular_phenotype|TTN-related_disorder|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_dominant_centronuclear_myopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Primary_dilated_cardiomyopathy|Heart_failure|TTN-related_disorder|Cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Ventricular_tachycardia|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|not_provided|Left_ventricular_noncompaction_cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|TTN-related_disorder|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Atrial_fibrillation|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|TTN-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Cardiomyopathy|Long_QT_syndrome|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|Limb-girdle_muscular_dystrophy|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiomyopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|not_provided|Tibial_muscular_dystrophy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|not_specified|not_provided|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_provided|Cardiomyopathy": 2,
    "not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Inborn_genetic_diseases|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "not_provided|TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified|TTN-related_disorder|Cardiomyopathy|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "TTN-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Limb-girdle_muscular_dystrophy|_recessive|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_dilated_cardiomyopathy|Tip-toe_gait": 1,
    "not_provided|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|TTN-related_disorder|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9": 1,
    "not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_specified": 1,
    "TTN-related_disorder|not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 1,
    "TTN-related_disorder|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "TTN-related_disorder|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 16,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Dilated_cardiomyopathy_1G|Cardiomyopathy|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Muscular_dystrophy|not_provided|Schizophrenia|Primary_dilated_cardiomyopathy": 1,
    "Tibial_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|TTN-related_disorder": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiomyopathy": 1,
    "Centronuclear_myopathy|Dilated_cardiomyopathy_1G": 1,
    "not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Hypertrophic_cardiomyopathy_2|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G": 1,
    "Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Primary_dilated_cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Hypertrophic_cardiomyopathy_9|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "TTN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy_9|not_specified|not_provided|Cardiomyopathy|Tip-toe_gait": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Arthrogryposis_syndrome|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiovascular_phenotype|Tibial_muscular_dystrophy": 1,
    "Cardiomyopathy|Abnormality_of_neuronal_migration|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Tibial_muscular_dystrophy|Cardiomyopathy|not_specified|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 1,
    "TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Cardiovascular_phenotype|not_specified|not_provided|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Long_QT_syndrome|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Hypertrophic_cardiomyopathy|Tibial_muscular_dystrophy|not_specified|Limb-girdle_muscular_dystrophy|_recessive|Dilated_Cardiomyopathy|_Dominant|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Cardiomyopathy|Tibial_muscular_dystrophy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided|Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|TTN-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Tibial_muscular_dystrophy|not_provided": 1,
    "not_specified|Tibial_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Cardiomyopathy|not_provided": 1,
    "TTN-related_disorder|not_provided|Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|not_specified": 1,
    "Cardiovascular_phenotype|TTN-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_specified|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Early-onset_myopathy_with_fatal_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_provided": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|TTN-related_disorder|not_provided|Dilated_cardiomyopathy_1G|Tibial_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_specified|not_provided|Brugada_syndrome|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Dilated_cardiomyopathy_1G|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|not_provided|TTN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_9|Dilated_cardiomyopathy_1G|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy": 1,
    "not_specified|Cardiomyopathy|Early-onset_myopathy_with_fatal_cardiomyopathy|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure": 1,
    "Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiovascular_phenotype|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified|Tibial_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Tibial_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|not_specified|Early-onset_myopathy_with_fatal_cardiomyopathy|Tibial_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Cardiovascular_phenotype|not_provided|TTN-related_disorder|Cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Tibial_muscular_dystrophy|Early-onset_myopathy_with_fatal_cardiomyopathy|not_specified": 1,
    "Tibial_muscular_dystrophy|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|not_provided|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Early-onset_myopathy_with_fatal_cardiomyopathy": 1,
    "Early-onset_myopathy_with_fatal_cardiomyopathy|Myopathy|_myofibrillar|_9|_with_early_respiratory_failure|Dilated_cardiomyopathy_1G|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2J|Tibial_muscular_dystrophy|Hypertrophic_cardiomyopathy_9": 1,
    "not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 16,
    "CCDC141-related_disorder|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism": 2,
    "CCDC141-related_disorder|not_specified": 2,
    "not_provided|CCDC141-related_disorder": 5,
    "CCDC141-related_disorder": 4,
    "CCDC141-related_disorder|not_provided": 3,
    "not_provided|not_specified|CCDC141-related_disorder|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Disorder_of_sexual_differentiation": 28,
    "CCDC141-related_disorder|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism|not_specified": 1,
    "not_specified|not_provided|CCDC141-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 101,
    "ITGA4-related_disorder": 6,
    "not_provided|ITGA4-related_disorder": 2,
    "ITGA4-related_disorder|not_specified|not_provided": 1,
    "ITGA4-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_26|not_provided": 4,
    "Retinitis_pigmentosa_26": 85,
    "Retinitis_pigmentosa_26|not_provided|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_26|Isolated_macular_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_26": 3,
    "Retinitis_pigmentosa_26|not_provided": 43,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_26": 6,
    "not_provided|Retinitis_pigmentosa_26": 46,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 3,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_26": 1,
    "Retinitis_pigmentosa|not_provided|CERKL-related_disorder": 1,
    "Retinitis_pigmentosa_26|Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_26|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_26": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_26": 4,
    "Retinitis_pigmentosa_26|Retinitis_pigmentosa": 3,
    "Retinitis_pigmentosa_26|Cone-rod_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_26|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_26": 6,
    "Retinitis_pigmentosa_26|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_26|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_26|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Retinitis_pigmentosa_26|Inborn_genetic_diseases": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_26|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_26|Retinitis_pigmentosa|not_specified": 2,
    "not_provided|Retinitis_pigmentosa_26|Retinal_dystrophy|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_26|not_provided": 1,
    "Retinitis_pigmentosa_26|Retinal_dystrophy|not_provided": 2,
    "not_specified|not_provided|Retinitis_pigmentosa_26": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_26": 2,
    "Retinitis_pigmentosa_26|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|CERKL-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_26|Retinitis_pigmentosa|not_provided": 5,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_26": 3,
    "Retinitis_pigmentosa_26|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "CERKL-related_retinopathy|CERKL-related_disorder|Cone_dystrophy|Retinal_pigment_epithelial_atrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy|Retinitis_pigmentosa_26|See_cases": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_26": 1,
    "CERKL-related_disorder": 1,
    "Retinitis_pigmentosa_26|not_provided|Stargardt_disease": 1,
    "Severe_photosensitivity|Macular_dystrophy|Adult-onset_night_blindness|Retinitis_pigmentosa_26": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_26|not_provided": 1,
    "Retinitis_pigmentosa_26|Retinal_pigment_epithelial_atrophy|Cone_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_26": 1,
    "CERKL-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_26": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_26": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa": 6,
    "not_provided|Retinal_dystrophy|not_specified|Retinitis_pigmentosa_26|Retinitis_pigmentosa": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Retinitis_pigmentosa_26": 1,
    "not_provided|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_26": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy|not_provided|Retinitis_pigmentosa_26": 1,
    "Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_26|not_provided": 1,
    "not_provided|CERKL-related_disorder": 1,
    "CERKL-related_disorder|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_26": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|not_specified|Retinitis_pigmentosa_26": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_26|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_26|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_26|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_26|Retinitis_pigmentosa": 1,
    "CERKL-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_26": 1,
    "Maturity-onset_diabetes_of_the_young_type_6": 32,
    "Maturity-onset_diabetes_of_the_young_type_6|not_provided": 4,
    "Maturity-onset_diabetes_of_the_young_type_6|NEUROD1-related_disorder|not_specified": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_6": 18,
    "Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus|not_provided": 12,
    "Maturity-onset_diabetes_of_the_young_type_6|not_provided|Type_2_diabetes_mellitus": 3,
    "not_provided|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_6": 11,
    "Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus|not_provided|NEUROD1-related_disorder": 1,
    "not_provided|NEUROD1-related_disorder": 3,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_6|not_provided": 8,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus": 4,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus|Retinal_dystrophy|Inborn_genetic_diseases|NEUROD1-related_disorder": 1,
    "NEUROD1-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_6": 1,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_6": 1,
    "Inborn_genetic_diseases|not_provided|Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus": 1,
    "NEUROD1-related_disorder|Maturity-onset_diabetes_of_the_young_type_6|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_6|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_6|not_provided|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_6|NEUROD1-related_disorder|not_specified|not_provided": 1,
    "not_specified|NEUROD1-related_disorder|not_provided": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_6|Monogenic_diabetes|Hypoinsulinemia|not_provided": 1,
    "NEUROD1-related_disorder|not_provided": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_6|Inborn_genetic_diseases|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus|Inborn_genetic_diseases": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Retinal_dystrophy|not_provided|Maturity-onset_diabetes_of_the_young_type_6": 1,
    "Maturity-onset_diabetes_of_the_young_type_6|Retinal_dystrophy": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus|not_specified": 1,
    "Retinal_dystrophy|Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_6|Type_2_diabetes_mellitus": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_6": 1,
    "PDE1A-related_disorder": 2,
    "FRZB-related_disorder|Osteoarthritis_susceptibility_1": 1,
    "Hypertrophic_cardiomyopathy_14": 717,
    "FRZB-related_disorder": 3,
    "Osteoarthritis_susceptibility_1|FRZB-related_disorder": 1,
    "Osteoarthritis": 3,
    "Neurodevelopmental_disorder|Focal_sensory_seizure_with_somatosensory_features|Autism_spectrum_disorder": 1,
    "Immunodeficiency_72_with_autoinflammation": 14,
    "NCKAP1-related_disorder": 16,
    "NCKAP1-related_disorder|not_provided": 1,
    "not_provided|NCKAP1-related_disorder": 1,
    "NCKAP1-associated_Neurodevelopmental_disorder": 2,
    "Autistic_behavior|Neurodevelopmental_abnormality": 1,
    "Normal_pregnancy|Gestational_diabetes_mellitus_uncontrolled": 2,
    "ZNF804A-related_disorder|not_provided": 4,
    "ZNF804A-related_disorder": 15,
    "not_specified|not_provided|ZNF804A-related_disorder": 2,
    "ZNF804A-related_disorder|not_specified": 1,
    "FSIP2-related_disorder": 111,
    "Spermatogenic_failure_34": 23,
    "FSIP2-related_disorder|not_provided": 15,
    "FSIP2-related_disorder|Spermatogenic_failure_34|not_provided": 2,
    "FSIP2-related_disorder|not_specified": 4,
    "FSIP2-related_disorder|not_specified|not_provided": 2,
    "not_specified|FSIP2-related_disorder": 3,
    "not_provided|FSIP2-related_disorder": 4,
    "not_specified|Spermatogenic_failure_34": 2,
    "Spermatogenic_failure_34|not_specified": 1,
    "IMMUNE_DYSREGULATION|_NEURODEVELOPMENTAL_DEFECTS|_AND_COLITIS|ITGAV_deficiency": 3,
    "ITGAV-related_disorder": 11,
    "ITGAV_deficiency|IMMUNE_DYSREGULATION|_NEURODEVELOPMENTAL_DEFECTS|_AND_COLITIS": 1,
    "not_provided|ITGAV-related_disorder": 1,
    "Lymphatic_malformation_8|not_provided": 2,
    "Lymphatic_malformation_8": 1,
    "Ehlers-Danlos_syndrome|_type_4": 1682,
    "Ehlers-Danlos_syndrome|_type_4|not_provided": 74,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 223,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 188,
    "not_provided|Ehlers-Danlos_syndrome|_type_4": 55,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4": 19,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified": 8,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided": 26,
    "Ehlers-Danlos_syndrome|_type_4|not_specified": 18,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder": 2,
    "not_provided|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 24,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_type_4": 6,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Connective_tissue_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4": 4,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "COL3A1-related_disorder": 11,
    "POLYMICROGYRIA_WITHOUT_VASCULAR-TYPE_EHLERS-DANLOS_SYNDROME|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 9,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 34,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 10,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided|not_specified": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided": 5,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 5,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 3,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|Ehlers-Danlos_syndrome|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 2,
    "COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 4,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified|not_provided": 3,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 9,
    "not_provided|not_specified|COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4|not_specified|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|COL3A1-related_disorder": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 6,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 17,
    "Aortic_aneurysm|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 19,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 3,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Aortic_dissection": 1,
    "COL3A1-related_disorder|not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4": 21,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 13,
    "Aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome": 2,
    "not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome": 1,
    "Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder": 3,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|_dominant_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided|not_specified": 1,
    "COL3A1-related_disorder|Ehlers-Danlos_syndrome|_type_4": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|COL3A1-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 4,
    "Familial_aortopathy|Ehlers-Danlos_syndrome|_type_4": 2,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 5,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder": 1,
    "COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|COL3A1-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|COL3A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_and_Soft_Tissue_Disorder|not_provided": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Familial_aortopathy|not_provided|not_specified|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided|Thoracic_aortic_aneurysm_or_dissection|COL3A1-related_disorder": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided": 3,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 1,
    "COL3A1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided|COL3A1-related_disorder": 1,
    "not_provided|COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified|not_provided|Ehlers-Danlos_syndrome": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 2,
    "not_provided|not_specified|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|not_provided": 2,
    "Familial_aortopathy|not_specified|not_provided|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "COL3A1-related_disorder|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|COL3A1-related_disorder|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Arterial_dissection|COL3A1-related_disorder|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Congenital_aneurysm_of_ascending_aorta|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Connective_tissue_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_specified": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|COLLAGEN_TYPE_III_POLYMORPHISM|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|not_provided": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Abnormality_of_neuronal_migration|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4|not_specified|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_dominant_type_4|Ehlers-Danlos_syndrome|_type_4": 1,
    "EHLERS-DANLOS_SYNDROME|_NONVASCULAR_VARIANT": 1,
    "Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|See_cases": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|See_cases": 1,
    "COL3A1-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|COL3A1-related_disorder|not_specified|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_type_4": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder|not_provided|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome": 1,
    "Connective_tissue_disorder|COL3A1-related_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder": 1,
    "Seizure|Connective_tissue_nevi|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|COL3A1-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_2": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_aortopathy": 2,
    "COL3A1-related_disorder|not_specified|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|COL3A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_aortopathy": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_type_4|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_specified": 1,
    "Ehlers-Danlos_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Ehlers-Danlos_syndrome|_type_4": 2,
    "Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_dominant_type_4": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified": 2,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "See_cases|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|_dominant_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder|not_specified": 1,
    "not_provided|COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_3": 1,
    "Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|not_provided|Connective_tissue_disorder": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Inborn_genetic_diseases": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder|Ehlers-Danlos_syndrome|_type_4|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|not_provided|not_specified": 1,
    "Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_3": 1,
    "Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "COL3A1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4|not_specified": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy|not_provided|Ehlers-Danlos_syndrome|_type_4": 1,
    "Ehlers-Danlos_syndrome|_type_4|Ehlers-Danlos_syndrome|_type_3": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL3A1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_type_4|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|Ehlers-Danlos_syndrome|_type_4|COL3A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|_type_4|Polymicrogyria_with_or_without_vascular-type_Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome_type_7A|not_provided": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome_type_7A": 9,
    "Ehlers-Danlos_syndrome_type_7A": 50,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome_type_7A": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_2": 45,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided": 2,
    "Ehlers-Danlos_syndrome_type_7A|not_provided": 10,
    "not_provided|Ehlers-Danlos_syndrome_type_7A": 4,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_2": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1": 2472,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 195,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 24,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 96,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 30,
    "COL5A2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 32,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 109,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 219,
    "Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A2-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided": 23,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 73,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 29,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified": 6,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 73,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2": 9,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|_2": 2,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1": 59,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 24,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Abnormal_bleeding|Thrombocytopenia": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 4,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_2": 2,
    "COL5A2-related_disorder": 11,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Marfan_syndrome": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "COL5A2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 7,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided": 7,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 6,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome_type_7A": 3,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Telecanthus|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 7,
    "not_provided|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome|_classic_type|_2": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Disproportionate_tall_stature|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 10,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome|Familial_aortopathy": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type|_2": 2,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|not_specified|not_provided": 2,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome_type_7A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 8,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 6,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 20,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome_type_7A|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_2|Thrombocytopenia|Abnormal_bleeding": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 2,
    "COL5A2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|COL5A2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|not_specified": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 6,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|not_specified|not_provided": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 4,
    "not_provided|Marfan_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|COL5A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome_type_7A|not_specified": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|not_provided": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|not_specified": 1,
    "Connective_tissue_disorder|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|not_provided": 6,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 3,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL5A2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_2": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Telecanthus|Neuropathic_spinal_arthropathy|Joint_hypermobility|Hyperextensible_skin": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A2-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Marfan_syndrome": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A2-related_disorder|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_specified|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|COL5A2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|COL5A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_specified": 1,
    "COL5A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|_2|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Ehlers-Danlos_syndrome_type_7A|not_specified": 1,
    "not_specified|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "Hemochromatosis_type_4": 205,
    "not_provided|Hemochromatosis_type_4": 9,
    "Hereditary_hemochromatosis": 935,
    "Hemochromatosis_type_4|not_provided": 7,
    "Hereditary_hemochromatosis|not_provided": 5,
    "Hemochromatosis_type_4|Inborn_genetic_diseases": 6,
    "SLC40A1-related_disorder": 6,
    "Inborn_genetic_diseases|Hemochromatosis_type_4|SLC40A1-related_disorder": 1,
    "Inborn_genetic_diseases|Hemochromatosis_type_4": 4,
    "Hemochromatosis_type_4|SLC40A1-related_disorder": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Hemochromatosis_type_4": 1,
    "SLC40A1-related_disorder|Hemochromatosis_type_4": 3,
    "Hemochromatosis_type_4|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hemochromatosis_type_4|SLC40A1-related_disorder": 1,
    "Hemochromatosis_type_4|not_specified": 3,
    "Hemochromatosis_type_1|Hemochromatosis_type_4": 1,
    "not_provided|not_specified|Hemochromatosis_type_4": 3,
    "Hemochromatosis_type_4|Hereditary_hemochromatosis": 1,
    "SLC40A1-related_disorder|not_provided|Hemochromatosis_type_4": 1,
    "Polyp_of_colon|not_provided": 1,
    "not_provided|PMS1-related_disorder": 1,
    "PMS1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Lynch_syndrome_1": 3,
    "Lynch_syndrome_4": 297,
    "not_specified|Ovarian_cancer": 6,
    "PMS1-related_disorder": 1,
    "not_specified|PMS1-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 10,
    "Polyp_of_colon": 1,
    "not_provided|not_specified|Lynch_syndrome_1": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_carcinoma": 2,
    "Lynch_syndrome_1|Ovarian_cancer": 1,
    "not_provided|PMS1-related_breast_cancer|not_specified": 1,
    "PMS1-related_breast_cancer": 1,
    "PMS1-related_disorder|Lynch_syndrome": 1,
    "Myostatin-related_muscle_hypertrophy": 38,
    "not_provided|Myostatin-related_muscle_hypertrophy": 8,
    "Myostatin-related_muscle_hypertrophy|not_provided": 3,
    "Myostatin-related_muscle_hypertrophy|MSTN-related_disorder": 1,
    "not_provided|Myostatin-related_muscle_hypertrophy|MSTN-related_disorder": 1,
    "MSTN-related_disorder": 2,
    "Myostatin-related_muscle_hypertrophy|not_provided|MSTN-related_disorder": 1,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 121,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency|not_provided": 8,
    "HIBCH-related_disorder|not_provided|not_specified|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 1,
    "not_provided|3-hydroxyisobutyryl-CoA_hydrolase_deficiency|Inborn_genetic_diseases": 1,
    "See_cases|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 1,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency|not_specified": 5,
    "not_provided|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 5,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 6,
    "HIBCH-related_disorder|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 2,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency|See_cases": 1,
    "HIBCH-related_disorder|not_provided|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 1,
    "not_provided|not_specified|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 1,
    "not_specified|not_provided|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 1,
    "not_specified|not_provided|HIBCH-related_disorder|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 1,
    "Neurodegeneration_due_to_3-hydroxyisobutyryl_coenzyme_A_hydrolase_deficiency": 1,
    "not_specified|3-hydroxyisobutyryl-CoA_hydrolase_deficiency": 3,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency|not_provided|HIBCH-related_disorder": 1,
    "3-hydroxyisobutyryl-CoA_hydrolase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|3-hydroxyisobutyryl-CoA_hydrolase_deficiency|not_provided": 2,
    "not_provided|3-hydroxyisobutyryl-CoA_hydrolase_deficiency|not_specified": 1,
    "Retinal_disorder|Cleft_palate": 3,
    "GLS-related_disorder": 26,
    "GLS-related_disorder|not_provided": 2,
    "Global_developmental_delay|_progressive_ataxia|_and_elevated_glutamine": 3,
    "Developmental_and_epileptic_encephalopathy|_71": 7,
    "not_provided|GLS-related_disorder": 4,
    "Inborn_genetic_diseases|GLS-related_disorder": 1,
    "Infantile_cataract|_skin_abnormalities|_glutamate_excess|_and_impaired_intellectual_development": 5,
    "not_provided|Global_developmental_delay|_progressive_ataxia|_and_elevated_glutamine": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 58,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 1,
    "Familial_Atypical_Mycobacteriosis|_Autosomal_Dominant": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided": 3,
    "Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 91,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B": 137,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 89,
    "not_provided|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 3,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 80,
    "STAT1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B": 3,
    "Inborn_genetic_diseases|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 2,
    "Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 37,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 2,
    "Inherited_Immunodeficiency_Diseases": 30,
    "STAT1-related_disorder|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided": 4,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided": 2,
    "STAT1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 4,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|not_provided": 4,
    "Immunodeficiency_31B": 10,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B": 24,
    "Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided": 4,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_specified|not_provided": 1,
    "STAT1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Inborn_genetic_diseases": 2,
    "STAT1-related_disorder": 6,
    "Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Inborn_genetic_diseases": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|not_provided": 2,
    "not_provided|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 3,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|not_provided": 2,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_specified": 1,
    "Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|not_provided": 3,
    "STAT1-related_disorder|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 4,
    "STAT1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|not_provided": 2,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_specified|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 2,
    "STAT1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided|not_specified|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|not_specified": 1,
    "Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|STAT1-Related_Immunodeficiency|Inborn_genetic_diseases": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|not_specified|not_provided": 1,
    "STAT1-related_disorder|Inherited_Immunodeficiency_Diseases|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|not_provided": 1,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|STAT1-related_disorder": 1,
    "Inborn_genetic_diseases|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "STAT1-related_disorder|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided|not_specified|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "Chronic_mucocutaneous_candidiasis": 2,
    "not_provided|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Inherited_Immunodeficiency_Diseases": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|STAT1-related_disorder|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|STAT1-related_disorder|See_cases|not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B": 1,
    "not_provided|STAT1-related_disorder|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Immunodeficiency_31B": 1,
    "Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_provided|Chronic_mucocutaneous_candidiasis": 1,
    "Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|not_specified": 1,
    "not_provided|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|not_provided|STAT1-related_disorder": 1,
    "Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Inherited_Immunodeficiency_Diseases": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B": 1,
    "not_provided|STAT1-related_disorder|Immunodeficiency_31B|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 1,
    "Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 1,
    "STAT1-related_disorder|not_provided|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 1,
    "Immunodeficiency_31B|not_provided": 1,
    "not_specified|not_provided|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome|Immunodeficiency_31B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_STAT1_deficiency": 1,
    "Disabling_pansclerotic_morphea_of_childhood": 2,
    "not_provided|Disabling_pansclerotic_morphea_of_childhood": 2,
    "STAT4-related_disorder": 2,
    "STAT4-related_disorder|not_provided": 8,
    "not_provided|STAT4-related_disorder": 2,
    "Systemic_lupus_erythematosus|_susceptibility_to|_11": 2,
    "DNAH7-related_disorder": 43,
    "Abdominal_situs_inversus|Primary_ciliary_dyskinesia|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|not_provided": 1,
    "DNAH7-related_disorder|not_provided": 14,
    "Ciliary_dyskinesia|_primary|_50": 16,
    "not_provided|DNAH7-related_disorder": 11,
    "Abnormal_muscle_tone|Seizure|Abnormal_basal_ganglia_morphology|Hypoplasia_of_the_corpus_callosum|Dyspnea": 1,
    "DNAH7-related_disorder|not_provided|not_specified": 6,
    "Primary_ciliary_dyskinesia|Abdominal_situs_inversus": 1,
    "Ciliary_dyskinesia|_primary|_50|DNAH7-related_disorder": 1,
    "not_specified|Ciliary_dyskinesia|_primary|_50": 1,
    "not_provided|DNAH7-related_disorder|not_specified": 1,
    "DNAH7-related_disorder|not_specified": 2,
    "not_specified|DNAH7-related_disorder|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_50|not_provided": 1,
    "not_specified|DNAH7-related_disorder": 1,
    "Primary_ciliary_dyskinesia_3": 371,
    "DNAH7-related_disorder|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|not_provided": 12,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language": 85,
    "HECW2-related_disorder|not_provided": 12,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language": 7,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Inborn_genetic_diseases": 3,
    "Intellectual_disability|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Inborn_genetic_diseases|not_provided|HECW2-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia": 1,
    "not_provided|HECW2-related_disorder": 2,
    "HECW2-related_disorder|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "HECW2-related_disorder": 10,
    "Inborn_genetic_diseases|HECW2-related_disorder|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|not_provided": 1,
    "HECW2-related_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language": 4,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Inborn_genetic_diseases|not_specified": 1,
    "HECW2-related_disorder|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|not_provided": 2,
    "HECW2-related_disorder|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|HECW2-related_disorder|not_provided": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Abnormality_of_the_nervous_system": 1,
    "Neurofibromatosis|_type_1|Intellectual_disability|not_provided|HECW2-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Inborn_genetic_diseases": 1,
    "HECW2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|HECW2-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|HECW2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|HECW2-related_disorder": 2,
    "not_provided|HECW2-related_disorder|Inborn_genetic_diseases": 1,
    "Oromandibular-limb_hypogenesis_spectrum|HECW2-related_disorder": 1,
    "HECW2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "See_cases|Inborn_genetic_diseases|not_provided": 3,
    "See_cases|Inborn_genetic_diseases": 14,
    "Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_disability|HECW2-related_disorder": 1,
    "Intellectual_disability|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language": 1,
    "GTF3C3-related_disorder": 8,
    "Chromosome_2q32-q33_deletion_syndrome": 519,
    "NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES|_BRAIN_ANOMALIES|_AND_SEIZURES": 8,
    "Chromosome_2q32-q33_deletion_syndrome|NEURODEVELOPMENTAL_DISORDER_WITH_DYSMORPHIC_FACIES|_BRAIN_ANOMALIES|_AND_SEIZURES": 1,
    "Intellectual_disability|_autosomal_recessive_42|Inborn_genetic_diseases": 7,
    "Intellectual_disability|_autosomal_recessive_42": 217,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_recessive_42": 1,
    "Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_recessive_42": 5,
    "Intellectual_disability|_autosomal_recessive_42|not_provided|Hereditary_spastic_paraplegia|PGAP1-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42": 10,
    "PGAP1-related_disorder|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42|not_specified": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 11,
    "not_specified|Intellectual_disability|_autosomal_recessive_42|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_42": 7,
    "Intellectual_disability|_autosomal_recessive_42|not_provided": 6,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42": 1,
    "Intellectual_disability|_autosomal_recessive_42|not_provided|PGAP1-related_disorder": 3,
    "Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_recessive_42|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_42|not_provided|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia|not_provided|Intellectual_disability|_autosomal_recessive_42": 1,
    "Intellectual_disability|_autosomal_recessive_42|not_specified|not_provided|Hereditary_spastic_paraplegia": 2,
    "Intellectual_disability|_autosomal_recessive_42|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42|Neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_42|not_specified": 3,
    "PGAP1-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_58|Intellectual_disability|_autosomal_recessive_42": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_42": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_42|Hereditary_spastic_paraplegia": 1,
    "Intellectual_disability|_autosomal_recessive_42|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 1,
    "Cerebral_visual_impairment_and_intellectual_disability|Intellectual_disability|_autosomal_recessive_42": 2,
    "Intellectual_disability|_autosomal_recessive_42|Hereditary_spastic_paraplegia": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_42|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_42|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_recessive_42": 1,
    "Hereditary_spastic_paraplegia|not_provided|Intellectual_disability|_autosomal_recessive_42|not_specified": 1,
    "not_provided|SF3B1-related_disorder": 3,
    "SF3B1-related_disorder": 7,
    "SF3B1-related_disorder|not_provided": 2,
    "not_provided|Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Myelodysplastic_syndrome|SF3B1-related_disorder": 1,
    "Myelodysplastic_syndrome_progressed_to_acute_myeloid_leukemia|Myelodysplastic_syndrome": 1,
    "Acute_myeloid_leukemia|Myelodysplastic_syndrome": 1,
    "Myelodysplastic_syndrome|not_specified": 2,
    "Myelodysplastic_syndrome": 8,
    "Hereditary_spastic_paraplegia_13": 20,
    "Hypomyelinating_leukodystrophy_4|Spastic_paraplegia": 3,
    "not_provided|Hereditary_spastic_paraplegia_13|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia": 1,
    "HSPD1-related_disorder": 3,
    "Hereditary_spastic_paraplegia_13|Spastic_paraplegia|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Spastic_paraplegia": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_13|Hypomyelinating_leukodystrophy_4": 2,
    "Hereditary_spastic_paraplegia_13|Spastic_paraplegia": 6,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_13|Spastic_paraplegia": 1,
    "Hypomyelinating_leukodystrophy_4": 8,
    "not_specified|Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_13|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_13|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_13|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_13|Hypomyelinating_leukodystrophy_4": 2,
    "Hereditary_spastic_paraplegia_13|not_specified|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|not_specified": 74,
    "Spastic_paraplegia|HSPD1-related_disorder": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_13": 2,
    "Hereditary_spastic_paraplegia|HSPD1-related_disorder|not_provided|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_13": 1,
    "HSPD1-related_disorder|Spastic_paraplegia|Hypomyelinating_leukodystrophy_4|Hereditary_spastic_paraplegia_13|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia": 41,
    "Hereditary_spastic_paraplegia_13|not_provided|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_13|Hypomyelinating_leukodystrophy_4|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_13": 1,
    "not_provided|Hereditary_spastic_paraplegia_13|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Leukodystrophy|Hypomyelinating_leukodystrophy_4": 1,
    "not_specified|Hereditary_spastic_paraplegia_13|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 1,
    "HSPD1-related_disorder|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_13": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_13": 1,
    "Hereditary_spastic_paraplegia_13|not_specified": 1,
    "Hereditary_spastic_paraplegia_13|not_specified|not_provided": 1,
    "HSPE1-related_condition": 1,
    "MARS2-related_disorder": 3,
    "Spastic_ataxia_3": 9,
    "MARS2-related_disorder|not_provided": 6,
    "Combined_oxidative_phosphorylation_defect_type_25|Spastic_ataxia_3|not_provided": 1,
    "not_provided|MARS2-related_disorder": 3,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_25|not_specified": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_25": 1,
    "Combined_oxidative_phosphorylation_defect_type_25": 3,
    "not_specified|not_provided|MARS2-related_disorder": 1,
    "not_provided|not_specified|Spastic_ataxia_3|Combined_oxidative_phosphorylation_defect_type_25": 1,
    "MARS2-related_disorder|Spastic_ataxia_3|Combined_oxidative_phosphorylation_defect_type_25|not_specified|not_provided": 1,
    "Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases": 22,
    "Chromosome_2q32-q33_deletion_syndrome|not_provided|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Chromosome_2q32-q33_deletion_syndrome": 15,
    "Chromosome_2q32-q33_deletion_syndrome|not_provided": 34,
    "Inborn_genetic_diseases|not_provided|Chromosome_2q32-q33_deletion_syndrome": 5,
    "not_provided|Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Chromosome_2q32-q33_deletion_syndrome|not_provided": 2,
    "not_specified|Chromosome_2q32-q33_deletion_syndrome": 4,
    "not_provided|Chromosome_2q32-q33_deletion_syndrome": 16,
    "Chromosome_2q32-q33_deletion_syndrome|SATB2-related_disorder": 5,
    "SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome": 8,
    "Chromosome_2q32-q33_deletion_syndrome|not_provided|not_specified": 1,
    "Global_developmental_delay|Micrognathia|Microcephaly|Hyperplasia_of_midface|Downturned_corners_of_mouth|Speech_articulation_difficulties|Abnormal_facial_shape": 1,
    "SATB2_associated_disorder": 4,
    "SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "SATB2-related_disorder": 10,
    "not_specified|not_provided|SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases": 1,
    "Chromosome_2q32-q33_deletion_syndrome|not_specified": 1,
    "Dolichocephaly|Abnormality_of_the_dentition|Clinodactyly_of_the_5th_finger|Global_developmental_delay|Macrocephaly|Cleft_palate|not_provided": 1,
    "Chromosome_2q32-q33_deletion_syndrome|not_provided|Global_developmental_delay": 1,
    "not_specified|not_provided|Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases": 2,
    "SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome|not_provided": 1,
    "Chromosome_2q32-q33_deletion_syndrome|SATB2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|Chromosome_2q32-q33_deletion_syndrome|Isolated_cleft_palate|Dystonic_disorder|Intellectual_disability|not_provided": 1,
    "Chromosome_2q32-q33_deletion_syndrome|Neurodevelopmental_abnormality|not_provided": 1,
    "SATB2_associated_disorder|Chromosome_2q32-q33_deletion_syndrome|not_provided|Intellectual_disability": 1,
    "Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases|not_provided|See_cases|Neurodevelopmental_disorder": 1,
    "SATB2_associated_disorder|not_provided|Inborn_genetic_diseases|Chromosome_2q32-q33_deletion_syndrome": 1,
    "Chromosome_2q32-q33_deletion_syndrome|SATB2-related_disorder|not_provided": 1,
    "SATB2-related_disorder|SATB2_associated_disorder|Inborn_genetic_diseases|Chromosome_2q32-q33_deletion_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Chromosome_2q32-q33_deletion_syndrome": 2,
    "Inborn_genetic_diseases|SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome": 1,
    "SATB2-related_disorder|not_provided|Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases": 1,
    "SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome|not_provided|Intellectual_disability|Cleft_palate": 1,
    "SATB2_associated_disorder|Chromosome_2q32-q33_deletion_syndrome": 1,
    "SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases": 1,
    "Chromosome_2q32-q33_deletion_syndrome|not_provided|SATB2-related_disorder": 1,
    "SATB2-related_disorder|not_provided": 2,
    "SATB2-associated_syndrome": 1,
    "Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases|SATB2-related_disorder": 1,
    "Inborn_genetic_diseases|SATB2-related_disorder|Chromosome_2q32-q33_deletion_syndrome|not_provided": 1,
    "Chromosome_2q32-q33_deletion_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_53": 9,
    "Combined_oxidative_phosphorylation_deficiency_53|not_provided": 1,
    "C2orf69-related_disorder": 2,
    "KCTD18-related_disorder|not_provided": 2,
    "KCTD18-related_disorder": 14,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_25": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_25|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|not_provided": 1,
    "Developmental_cataract|Death_in_childhood|Developmental_regression|Seizure|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_25|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A": 398,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_2A": 24,
    "Autoimmune_lymphoproliferative_syndrome_type_1|Autoimmune_lymphoproliferative_syndrome_type_2A": 5,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|Diffuse_midline_glioma|_H3_K27-altered": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|not_specified": 18,
    "not_specified|Autoimmune_lymphoproliferative_syndrome_type_2A": 24,
    "not_specified|not_provided|Autoimmune_lymphoproliferative_syndrome_type_2A": 2,
    "CASP10-related_disorder": 7,
    "not_provided|CASP10-related_disorder|Autoimmune_lymphoproliferative_syndrome_type_2A": 1,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_2A|not_specified": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|Lymphoma|_non-Hodgkin|_familial|Gastric_cancer|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|not_provided": 4,
    "Neoplasm_of_stomach|Autoimmune_lymphoproliferative_syndrome_type_2A": 1,
    "Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_1|Autoimmune_lymphoproliferative_syndrome_type_2A": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|CASP10-related_disorder": 7,
    "CASP10-related_disorder|not_specified|Autoimmune_lymphoproliferative_syndrome_type_2A": 1,
    "CASP10-related_disorder|Autoimmune_lymphoproliferative_syndrome_type_2A": 2,
    "Gastric_cancer|Non-Hodgkin_lymphoma": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|Lymphoma|_non-Hodgkin|_familial|Gastric_cancer": 2,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|not_provided|Lymphoma|_non-Hodgkin|_familial|Gastric_cancer": 1,
    "not_specified|CASP10-related_disorder|not_provided|Autoimmune_lymphoproliferative_syndrome_type_2A": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|Autoimmune_lymphoproliferative_syndrome_type_1|CASP10-related_disorder|Lymphoma|_non-Hodgkin|_familial|Gastric_cancer|not_provided": 1,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_2A|Hypomyelination_and_Congenital_Cataract": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|Neoplasm_of_stomach|Lymphoma|_non-Hodgkin|_familial|Gastric_cancer|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|Gastric_cancer|Lymphoma|_non-Hodgkin|_familial": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|not_provided|CASP10-related_disorder": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2A|not_provided|not_specified": 1,
    "Neoplasm_of_stomach": 1,
    "Lung_cancer|_protection_against": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2B": 261,
    "not_specified|Autoimmune_lymphoproliferative_syndrome_type_2B|not_provided": 1,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome_type_2B": 15,
    "Autoimmune_lymphoproliferative_syndrome_type_2B|Lung_cancer|Hepatocellular_carcinoma|Familial_cancer_of_breast|Inborn_genetic_diseases": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2B|not_provided": 12,
    "Autoimmune_lymphoproliferative_syndrome_type_2B|Inborn_genetic_diseases": 3,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_2B": 4,
    "Autoimmune_lymphoproliferative_syndrome_type_2B|not_provided|not_specified": 2,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_2B|Hepatocellular_carcinoma|Familial_cancer_of_breast|Lung_cancer": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2B|not_provided|CASP8-related_disorder": 1,
    "CASP8-related_disorder|not_provided": 1,
    "CASP8-related_disorder": 2,
    "CASP8-related_disorder|Autoimmune_lymphoproliferative_syndrome_type_2B": 1,
    "not_provided|not_specified|Autoimmune_lymphoproliferative_syndrome_type_2B|BREAST_CANCER|_PROTECTION_AGAINST": 1,
    "Hepatocellular_carcinoma": 15,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_2B|not_specified": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_2B|not_provided|Inborn_genetic_diseases": 1,
    "Spermatogenic_failure_68": 2,
    "Joubert_syndrome_14": 331,
    "not_provided|Joubert_syndrome_14": 12,
    "Joubert_syndrome_14|Inborn_genetic_diseases": 12,
    "TMEM237-related_disorder": 6,
    "Joubert_syndrome_14|not_specified": 7,
    "not_provided|Joubert_syndrome_14|not_specified": 4,
    "Joubert_syndrome_14|not_specified|not_provided": 2,
    "Joubert_syndrome_14|Inborn_genetic_diseases|not_provided": 1,
    "TMEM237-related_disorder|not_provided|Joubert_syndrome_14": 3,
    "not_specified|not_provided|Joubert_syndrome_14": 3,
    "not_specified|Joubert_syndrome_14|Joubert_syndrome_1": 1,
    "Joubert_syndrome_14|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_14": 11,
    "Joubert_syndrome_14|not_provided": 8,
    "Joubert_syndrome|Joubert_syndrome_14|not_specified|not_provided": 1,
    "not_specified|Joubert_syndrome_14": 5,
    "Joubert_syndrome_14|Meckel-Gruber_syndrome": 1,
    "TMEM237-related_disorder|Joubert_syndrome_14|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_14|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_14": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_14|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_14|not_provided": 1,
    "Joubert_syndrome_14|not_provided|TMEM237-related_disorder": 1,
    "not_provided|not_specified|Joubert_syndrome_14": 2,
    "not_specified|Joubert_syndrome_14|not_provided": 1,
    "not_provided|TMEM237-related_disorder|Joubert_syndrome_14|Inborn_genetic_diseases": 1,
    "TMEM237-related_disorder|not_specified|not_provided|Joubert_syndrome_14": 1,
    "Joubert_syndrome_14|TMEM237-related_disorder": 1,
    "Joubert_syndrome_14|Joubert_syndrome": 1,
    "TMEM237-related_disorder|Joubert_syndrome_and_related_disorders|not_provided|Joubert_syndrome_14|Joubert_syndrome": 1,
    "Joubert_syndrome|not_provided": 51,
    "Global_developmental_delay|Generalized_hypotonia|Strabismus|Wide_nasal_bridge|High_palate|Seizure|Intellectual_disability": 1,
    "ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 32,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder": 11,
    "ALS2-related_disorder|Amyotrophic_Lateral_Sclerosis|_Recessive": 1,
    "ALS2-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 5,
    "not_specified|Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis": 2,
    "ALS2-related_disorder|Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis": 568,
    "not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis|Inborn_genetic_diseases": 2,
    "ALS2-related_disorder": 3,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_motor_neuron_disease|Microcephaly": 1,
    "not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 19,
    "Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile": 16,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Inborn_genetic_diseases": 12,
    "Limb_dystonia|Abnormal_cerebral_white_matter_morphology|Hypertyrosinemia|Global_developmental_delay|Hypokinesia|Spasticity": 1,
    "ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 4,
    "Juvenile_primary_lateral_sclerosis|Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "not_provided|not_specified|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|Juvenile_primary_lateral_sclerosis": 1,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder|Juvenile_primary_lateral_sclerosis|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 3,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_specified|Infantile-onset_ascending_hereditary_spastic_paralysis|Hereditary_spastic_paraplegia": 1,
    "ALS2-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|not_specified": 1,
    "Amyotrophic_Lateral_Sclerosis|_Recessive|ALS2-related_disorder": 4,
    "Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided": 1,
    "Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis": 22,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Juvenile_amyotrophic_lateral_sclerosis": 1,
    "Juvenile_primary_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 3,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided": 16,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Hereditary_spastic_paraplegia": 5,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis": 1,
    "ALS2-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "ALS2-related_disorder|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Hereditary_spastic_paraplegia|Infantile-onset_ascending_hereditary_spastic_paralysis|Peripheral_axonal_neuropathy|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "Juvenile_primary_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_specified|ALS2-related_disorder|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis|Juvenile_primary_lateral_sclerosis": 1,
    "ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_motor_neuron_disease": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Hereditary_spastic_paraplegia|ALS2-related_disorder|not_specified|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 4,
    "not_specified|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 2,
    "Hereditary_spastic_paraplegia|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_specified|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder": 1,
    "Amyotrophic_Lateral_Sclerosis|_Recessive|ALS2-related_disorder|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Amyotrophic_lateral_sclerosis|Infantile-onset_ascending_hereditary_spastic_paralysis": 2,
    "Juvenile_primary_lateral_sclerosis": 5,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "ALS2-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 2,
    "not_provided|Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_specified|Infantile-onset_ascending_hereditary_spastic_paralysis": 3,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided|Inborn_genetic_diseases": 2,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Juvenile_primary_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|Tip-toe_gait": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|Juvenile_primary_lateral_sclerosis": 2,
    "ALS2-related_motor_neuron_disease|not_provided": 1,
    "not_specified|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "not_specified|Hereditary_spastic_paraplegia|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|ALS2-related_motor_neuron_disease|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_specified|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 2,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided|not_specified|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "Hereditary_spastic_paraplegia|ALS2-related_disorder|not_provided|ALS2-related_motor_neuron_disease|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Inborn_genetic_diseases|not_provided": 4,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder": 1,
    "ALS2-related_motor_neuron_disease|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|not_specified": 1,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|Tip-toe_gait|Peripheral_axonal_neuropathy|ALS2-related_disorder|Hereditary_spastic_paraplegia": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis|ALS2-related_disorder|not_specified|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Inborn_genetic_diseases|not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis": 3,
    "not_provided|Hereditary_spastic_paraplegia|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_provided|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Juvenile_primary_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Juvenile_primary_lateral_sclerosis|Infantile-onset_ascending_hereditary_spastic_paralysis": 2,
    "not_specified|ALS2-related_disorder|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided": 1,
    "not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis|not_specified": 1,
    "not_provided|Amyotrophic_Lateral_Sclerosis|_Recessive|Hereditary_spastic_paraplegia|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided|ALS2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_2|_juvenile|ALS2-related_disorder": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided|Abnormal_central_motor_function": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|Hereditary_spastic_paraplegia|ALS2-related_disorder|not_provided": 1,
    "not_provided|Juvenile_primary_lateral_sclerosis": 1,
    "ALS2-related_motor_neuron_disease": 1,
    "ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided|ALS2-related_disorder": 1,
    "ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis|Juvenile_primary_lateral_sclerosis|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "Juvenile_primary_lateral_sclerosis|not_provided|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_specified|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "not_provided|Hereditary_spastic_paraplegia|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_provided": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|not_specified": 1,
    "Inborn_genetic_diseases|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "not_provided|Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Abnormal_central_motor_function": 12,
    "ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis": 1,
    "not_provided|Hereditary_spastic_paraplegia|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Juvenile_primary_lateral_sclerosis|not_specified": 1,
    "Inborn_genetic_diseases|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "ALS2-related_disorder|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "ALS2-related_disorder|not_specified|Hereditary_spastic_paraplegia|ALS2-related_motor_neuron_disease|Infantile-onset_ascending_hereditary_spastic_paralysis|Amyotrophic_lateral_sclerosis_type_2|_juvenile": 1,
    "Infantile-onset_ascending_hereditary_spastic_paralysis|ALS2-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_2|_juvenile|not_specified|ALS2-related_disorder|Infantile-onset_ascending_hereditary_spastic_paralysis|not_provided": 1,
    "Juvenile_primary_lateral_sclerosis|not_specified|not_provided|ALS2-related_disorder|Amyotrophic_lateral_sclerosis_type_2|_juvenile|Infantile-onset_ascending_hereditary_spastic_paralysis": 1,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "Orofacial_cleft_10|not_provided": 1,
    "Pulmonary_hypertension|_primary|_1": 402,
    "Pulmonary_hypertension|_primary|_1|not_provided": 22,
    "BMPR2-related_disorder": 6,
    "not_provided|Pulmonary_hypertension|_primary|_1": 13,
    "not_provided|Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1": 2,
    "not_provided|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_specified|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1": 6,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 51,
    "not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|BMPR2-related_disorder|Primary_pulmonary_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension": 25,
    "Primary_pulmonary_hypertension|Inborn_genetic_diseases|not_provided|Pulmonary_hypertension|_primary|_1": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1": 2,
    "Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1": 25,
    "Primary_pulmonary_hypertension|Inborn_genetic_diseases": 54,
    "Primary_pulmonary_hypertension": 174,
    "not_provided|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 3,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 8,
    "Pulmonary_venoocclusive_disease_1|Pulmonary_hypertension|_primary|_1": 2,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 2,
    "Pulmonary_arterial_hypertension|BMPR2-related_disorder|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension|not_provided|Inborn_genetic_diseases": 1,
    "Pulmonary_venoocclusive_disease_1|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 2,
    "Inborn_genetic_diseases|Primary_pulmonary_hypertension": 39,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 2,
    "Primary_pulmonary_hypertension|Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 3,
    "Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases|Primary_pulmonary_hypertension": 1,
    "Pulmonary_arterial_hypertension|Inborn_genetic_diseases|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|not_provided|BMPR2-related_disorder": 1,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 19,
    "Pulmonary_venoocclusive_disease_1": 6,
    "Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_arterial_hypertension": 2,
    "not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 2,
    "Inborn_genetic_diseases|not_provided|Primary_pulmonary_hypertension": 2,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension|Inborn_genetic_diseases": 1,
    "BMPR2-related_disorder|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension|not_provided": 1,
    "Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Inborn_genetic_diseases": 2,
    "Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_provided": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1": 1,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 19,
    "Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease": 8,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension": 49,
    "Inborn_genetic_diseases|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension": 1,
    "Inborn_genetic_diseases|Primary_pulmonary_hypertension|BMPR2-related_disorder": 1,
    "Pulmonary_hypertension|_primary|_dexfenfluramine-associated": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 5,
    "BMPR2-related_disorder|Pulmonary_hypertension|_primary|_1": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_arterial_hypertension_associated_with_connective_tissue_disease": 1,
    "Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases": 5,
    "Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 3,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|not_provided": 2,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|not_provided|Primary_pulmonary_hypertension": 1,
    "not_provided|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease": 3,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|not_specified|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|not_provided": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|not_provided|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 1,
    "not_provided|Pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Primary_pulmonary_hypertension": 1,
    "Drug-_or_toxin-induced_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|not_provided": 1,
    "not_provided|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension": 5,
    "Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 7,
    "Primary_pulmonary_hypertension|not_provided|Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_fenfluramine-associated|Pulmonary_hypertension|_primary|_1": 1,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Pulmonary_venoocclusive_disease_1": 1,
    "not_provided|not_specified|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Inborn_genetic_diseases": 1,
    "Pulmonary_venoocclusive_disease_1|Familial_pulmonary_capillary_hemangiomatosis": 1,
    "Primary_pulmonary_hypertension|not_provided": 1,
    "Primary_pulmonary_hypertension|BMPR2-related_disorder|not_provided|Pulmonary_hypertension|_primary|_1": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_hypertension|_primary|_dexfenfluramine-associated": 1,
    "not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Primary_pulmonary_hypertension|not_provided|Pulmonary_hypertension|_primary|_1": 1,
    "Inborn_genetic_diseases|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1": 2,
    "not_provided|Primary_pulmonary_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Inborn_genetic_diseases": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_arterial_hypertension_associated_with_connective_tissue_disease|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|not_provided|BMPR2-related_disorder|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Inborn_genetic_diseases": 17,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|not_provided": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|not_provided": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 3,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension|not_provided": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Inborn_genetic_diseases|Primary_pulmonary_hypertension": 3,
    "Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_hypertension": 1,
    "not_provided|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|not_provided|Pulmonary_arterial_hypertension": 1,
    "not_provided|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases": 1,
    "Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_provided|Pulmonary_hypertension|_primary|_1": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Inborn_genetic_diseases|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 1,
    "Genetic_non-acquired_premature_ovarian_failure|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Tooth_agenesis|_selective|_1|Pulmonary_arterial_hypertension": 1,
    "not_provided|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Inborn_genetic_diseases|BMPR2-related_disorder": 1,
    "Pulmonary_arterial_hypertension|not_provided|Progressive_myositis_ossificans": 1,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|not_provided": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_provided": 2,
    "Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_arterial_hypertension": 2,
    "Pulmonary_hypertension|_primary|_1|not_provided|Inborn_genetic_diseases": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 2,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension": 2,
    "Inborn_genetic_diseases|Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|_with_hereditary_hemorrhagic_telangiectasia|Pulmonary_hypertension|_primary|_1": 1,
    "Primary_pulmonary_hypertension|Inborn_genetic_diseases|not_provided": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension": 1,
    "Tooth_agenesis|_selective|_1": 11,
    "Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_dexfenfluramine-associated|Pulmonary_hypertension|_primary|_1": 1,
    "not_provided|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension": 2,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|BMPR2-related_disorder|not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_venoocclusive_disease_1|Pulmonary_hypertension|_primary|_1|not_provided|Primary_pulmonary_hypertension": 1,
    "Genetic_non-acquired_premature_ovarian_failure|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|not_provided": 2,
    "Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_arterial_hypertension_associated_with_connective_tissue_disease|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|not_provided": 1,
    "Genetic_non-acquired_premature_ovarian_failure|Primary_pulmonary_hypertension": 1,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1": 1,
    "Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 3,
    "Primary_pulmonary_hypertension|Inborn_genetic_diseases|not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Primary_pulmonary_hypertension|Pulmonary_venoocclusive_disease_1|Pulmonary_hypertension|_primary|_1": 1,
    "Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|BMPR2-related_disorder": 1,
    "BMPR2-related_disorder|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension": 1,
    "Pulmonary_venoocclusive_disease_1|Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Inborn_genetic_diseases": 1,
    "Pulmonary_arterial_hypertension|Pulmonary_venoocclusive_disease_1|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases": 1,
    "Pulmonary_arterial_hypertension_associated_with_another_disease": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|not_provided": 1,
    "Pulmonary_arterial_hypertension_associated_with_another_disease|Pulmonary_arterial_hypertension_associated_with_HIV_infection|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|not_provided|Inborn_genetic_diseases": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_provided": 1,
    "not_specified|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|not_provided": 1,
    "Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Primary_pulmonary_hypertension": 1,
    "Drug-_or_toxin-induced_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Inborn_genetic_diseases": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1": 1,
    "Pulmonary_hypertension|_primary|_1|Primary_pulmonary_hypertension|Pulmonary_arterial_hypertension|Genetic_non-acquired_premature_ovarian_failure": 1,
    "Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Inborn_genetic_diseases": 1,
    "Pulmonary_arterial_hypertension|not_provided|Pulmonary_hypertension|_primary|_1|Pulmonary_venoocclusive_disease_1|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Primary_pulmonary_hypertension": 1,
    "Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|not_specified": 1,
    "Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Primary_pulmonary_hypertension|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Primary_pulmonary_hypertension|Pulmonary_hypertension|_primary|_1|Pulmonary_arterial_hypertension|Mitral_valve_prolapse|Right_ventricular_hypertrophy|Pulmonary_artery_dilatation|Right_ventricular_dilatation|Elevated_right_atrial_pressure|Increased_pulmonary_vascular_resistance|Complete_right_bundle_branch_block": 1,
    "BMPR2-related_disorder|Inborn_genetic_diseases": 1,
    "ABI2-related_disorder|not_specified": 1,
    "Immunodeficiency_123_with_HPV-related_verrucosis": 1,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 196,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 4,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|CTLA4-related_disorder": 3,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_specified|not_provided|Hashimoto_thyroiditis|_susceptibility_to": 1,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_provided": 8,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_specified": 1,
    "Systemic_lupus_erythematosus|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Type_1_diabetes_mellitus_12|Celiac_disease|_susceptibility_to|_3|Hashimoto_thyroiditis|Inborn_genetic_diseases|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Inherited_Immunodeficiency_Diseases": 1,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Type_1_diabetes_mellitus_12|Celiac_disease|_susceptibility_to|_3|Hashimoto_thyroiditis|Systemic_lupus_erythematosus|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_provided|Inherited_Immunodeficiency_Diseases": 1,
    "Immunodeficiency|_common_variable|_1": 138,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Inborn_genetic_diseases": 3,
    "Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Inborn_genetic_diseases|not_specified": 1,
    "Type_1_diabetes_mellitus_12|Celiac_disease|_susceptibility_to|_3|Hashimoto_thyroiditis|Systemic_lupus_erythematosus|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 1,
    "Type_1_diabetes_mellitus_12|Celiac_disease|_susceptibility_to|_3|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Systemic_lupus_erythematosus|Hashimoto_thyroiditis|not_provided": 1,
    "CTLA4-related_disorder|Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 1,
    "not_specified|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 1,
    "Hashimoto_thyroiditis|Systemic_lupus_erythematosus|Type_1_diabetes_mellitus_12|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|Celiac_disease|_susceptibility_to|_3|not_provided": 1,
    "CTLA4-related_disorder": 2,
    "CTLA4-related_disorder|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency": 1,
    "chronic_fatigue_syndrome_with_infection-triggered_onset|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_provided": 1,
    "not_provided|Immunodeficiency|_common_variable|_1|ICOS-related_disorder": 2,
    "Immunodeficiency|_common_variable|_1|Inherited_Immunodeficiency_Diseases": 2,
    "not_provided|Immunodeficiency|_common_variable|_1": 11,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_1": 2,
    "Immunodeficiency|_common_variable|_1|not_provided": 2,
    "Immunodeficiency|_common_variable|_1|not_specified": 1,
    "Immunodeficiency|_common_variable|_1|Inborn_genetic_diseases": 1,
    "Immunodeficiency|_common_variable|_1|Inborn_genetic_diseases|not_provided": 1,
    "Immunodeficiency|_common_variable|_1|ICOS-related_disorder": 1,
    "not_provided|ICOS-related_disorder|not_specified|Immunodeficiency|_common_variable|_1": 1,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_1": 3,
    "ICOS-related_disorder|Immunodeficiency|_common_variable|_1": 1,
    "ICOS-related_disorder|not_provided|Immunodeficiency|_common_variable|_1": 1,
    "PARD3B-related_disorder": 6,
    "PARD3B-related_disorder|not_provided": 1,
    "PARD3B-related_disorder|not_specified": 1,
    "not_specified|NRP2-related_disorder": 15,
    "NRP2-related_disorder": 237,
    "NRP2-related_disorder|not_specified": 15,
    "not_provided|NRP2-related_disorder": 7,
    "NRP2-related_disorder|not_provided": 14,
    "Hirschsprung_disease|_susceptibility_to|_1|NRP2-related_disorder|not_provided": 1,
    "NRP2-related_disorder|Inborn_genetic_diseases": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 105,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome": 71,
    "Mitochondrial_complex_I_deficiency|Leigh_syndrome": 13,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 36,
    "Leigh_syndrome|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 6,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 14,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 8,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_provided": 9,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_5": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_5": 8,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5": 26,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_specified|not_provided": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_5": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided": 7,
    "NDUFS1-related_disorder": 7,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Inborn_genetic_diseases|Leigh_syndrome": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Inborn_genetic_diseases": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases|not_provided|Leigh_syndrome": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided|Leigh_syndrome|Inborn_genetic_diseases|See_cases|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided|See_cases": 1,
    "Mitochondrial_complex_I_deficiency|not_provided|Leigh_syndrome": 4,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome": 12,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_5": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_5|NDUFS1-related_disorder|Mitochondrial_complex_I_deficiency|not_specified|not_provided|Leigh_syndrome": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided": 1,
    "NDUFS1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided": 1,
    "Leigh_syndrome|not_provided|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided": 4,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided": 1,
    "NDUFS1-related_disorder|not_provided": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases|not_provided": 4,
    "MELAS_syndrome": 426,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|See_cases": 1,
    "Leigh_syndrome|not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFS1-related_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_specified": 4,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|Mitochondrial_complex_I_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|NDUFS1-related_disorder": 1,
    "NDUFS1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided|Leigh_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_5": 1,
    "not_provided|NDUFS1-related_disorder": 2,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided": 2,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 3,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_5": 1,
    "NDUFS1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_5|not_provided": 1,
    "Moderate_global_developmental_delay|Seizure|Intellectual_disability": 1,
    "EEF1B2-related_condition": 1,
    "Nasopalpebral_lipoma-coloboma_syndrome|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 179,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 15,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "Combined_oxidative_phosphorylation_deficiency_44|not_specified|not_provided": 2,
    "Combined_oxidative_phosphorylation_deficiency_44|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 3,
    "Combined_oxidative_phosphorylation_deficiency_44": 61,
    "FASTKD2-related_disorder": 4,
    "FASTKD2-related_disorder|not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Combined_oxidative_phosphorylation_deficiency_44|not_provided": 18,
    "FASTKD2-related_disorder|not_provided": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Combined_oxidative_phosphorylation_deficiency_44|not_provided": 2,
    "not_provided|FASTKD2-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_specified|FASTKD2-related_disorder|Combined_oxidative_phosphorylation_deficiency_44|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_44": 11,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency_44": 5,
    "Combined_oxidative_phosphorylation_deficiency_44|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_44|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_deficiency_44": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Combined_oxidative_phosphorylation_deficiency_44": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Combined_oxidative_phosphorylation_deficiency_44": 3,
    "Combined_oxidative_phosphorylation_deficiency_44|Inborn_genetic_diseases|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Combined_oxidative_phosphorylation_deficiency_44": 1,
    "FASTKD2-related_disorder|Combined_oxidative_phosphorylation_deficiency_44|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_44|Leigh_syndrome": 2,
    "Combined_oxidative_phosphorylation_deficiency_44|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Combined_oxidative_phosphorylation_deficiency_44|Inborn_genetic_diseases": 2,
    "Combined_oxidative_phosphorylation_deficiency_44|Leigh_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency_44|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_44|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|FASTKD2-related_disorder": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified": 3,
    "not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 3,
    "not_provided|not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "FASTKD2-related_disorder|Combined_oxidative_phosphorylation_deficiency_44": 1,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_deficiency_44": 2,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_44|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified|not_provided": 1,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Combined_oxidative_phosphorylation_deficiency_44|Inborn_genetic_diseases": 1,
    "FASTKD2-related_disorder|not_provided|Combined_oxidative_phosphorylation_deficiency_44": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Combined_oxidative_phosphorylation_deficiency_44|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|FASTKD2-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Inborn_genetic_diseases|not_provided|FASTKD2-related_disorder|Combined_oxidative_phosphorylation_deficiency_44|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Combined_oxidative_phosphorylation_deficiency_44|not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 9,
    "KLF7-related_neurodevelopmental_disorder": 2,
    "KLF7-related_disorder|intellectual_deficiency|not_provided|Neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder|Anxiety|Intellectual_disability|KLF7-related_neurodevelopmental_disorder|not_provided|Inborn_genetic_diseases|Delayed_gross_motor_development|Mild_expressive_language_delay|KLF7-related_disorder": 1,
    "KLF7-related_disorder": 5,
    "KLF7-related_disorder|not_provided": 1,
    "Angiomatoid_fibrous_histiocytoma": 1,
    "not_provided|FZD5-related_disorder": 6,
    "FZD5-related_disorder|not_provided": 3,
    "Microphthalmia/coloboma_11": 6,
    "Microphthalmia/coloboma_11|Congenital_ocular_coloboma": 1,
    "Congenital_ocular_coloboma": 13,
    "FZD5-related_disorder": 2,
    "Cataract_4_multiple_types|not_specified|not_provided": 1,
    "Cataract_4_multiple_types|Aculeiform_cataract": 3,
    "CRYGD-related_disorder|Cataract_4_multiple_types|Aculeiform_cataract|Inborn_genetic_diseases": 1,
    "Aculeiform_cataract|Cataract_4_multiple_types": 2,
    "not_provided|Aculeiform_cataract": 3,
    "Aculeiform_cataract|not_provided": 1,
    "Cataract_4_multiple_types": 12,
    "Cataract_4_multiple_types|Developmental_cataract": 1,
    "Aculeiform_cataract|Inborn_genetic_diseases": 2,
    "CRYGD-related_disorder|Aculeiform_cataract|Inborn_genetic_diseases|Cataract_4_multiple_types": 1,
    "Aculeiform_cataract": 12,
    "Cataract_4_multiple_types|CRYGD-related_disorder|Aculeiform_cataract|not_provided": 1,
    "Inborn_genetic_diseases|Aculeiform_cataract": 1,
    "not_specified|Cataract_4_multiple_types|not_provided|Aculeiform_cataract": 1,
    "CRYGD-related_disorder": 4,
    "not_provided|Cataract_4_multiple_types|CRYGD-related_disorder|Aculeiform_cataract": 1,
    "Aculeiform_cataract|CRYGD-related_disorder": 1,
    "Cataract_4_multiple_types|Aculeiform_cataract|not_provided": 3,
    "Cataract_4_multiple_types|not_provided": 2,
    "not_specified|Cataract_4_multiple_types": 1,
    "Aculeiform_cataract|High_myopia|not_specified|CRYGD-related_disorder": 1,
    "Cataract_4_multiple_types|Aculeiform_cataract|CRYGD-related_disorder": 1,
    "Joubert_syndrome_17|Cataract_4_multiple_types|CRYGD-related_disorder|Aculeiform_cataract|not_provided": 1,
    "Aculeiform_cataract|not_provided|Inborn_genetic_diseases": 1,
    "CRYGD-related_disorder|not_provided": 1,
    "Developmental_cataract|Aculeiform_cataract|CRYGD-related_disorder|not_provided|Cataract_4_multiple_types": 1,
    "Aculeiform_cataract|not_specified|Cataract_4_multiple_types|not_provided": 1,
    "not_provided|Cataract_4_multiple_types|Aculeiform_cataract|not_specified": 1,
    "CRYGD-related_disorder|Cataract_4_multiple_types|Aculeiform_cataract": 1,
    "not_specified|Aculeiform_cataract|not_provided": 1,
    "not_provided|Cataract_4_multiple_types": 1,
    "Cataract": 13,
    "CRYGC-related_disorder": 5,
    "Nuclear_pulverulent_cataract|Cataract_2|_multiple_types": 1,
    "Developmental_cataract|Cataract_2|_multiple_types": 1,
    "CRYGC-related_disorder|Nuclear_pulverulent_cataract": 5,
    "Cataract_2|_multiple_types": 11,
    "Cataract_2|_multiple_types|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Nuclear_pulverulent_cataract": 5,
    "Nuclear_pulverulent_cataract": 22,
    "Nuclear_pulverulent_cataract|not_provided": 2,
    "Nuclear_pulverulent_cataract|CRYGC-related_disorder": 1,
    "not_provided|Nuclear_pulverulent_cataract": 2,
    "CRYGC-related_disorder|Inborn_genetic_diseases": 1,
    "Nuclear_pulverulent_cataract|Inborn_genetic_diseases": 3,
    "Nuclear_pulverulent_cataract|Usher_syndrome_type_2C|not_specified|not_provided": 1,
    "Cataract_2|_multiple_types|Nuclear_pulverulent_cataract": 1,
    "Cataract_2|_Coppock-like|Nuclear_pulverulent_cataract": 1,
    "CRYGB-related_disorder": 3,
    "Cataract_39_multiple_types": 9,
    "Cataract_39_multiple_types|not_specified": 2,
    "not_provided|Cataract_39_multiple_types": 2,
    "Cataract_39_multiple_types|CRYGB-related_disorder": 1,
    "not_specified|Cataract_39_multiple_types": 3,
    "CRYGB-related_disorder|Cataract_39_multiple_types": 1,
    "Cataract_39_multiple_types|not_provided": 3,
    "CRYGA-related_disorder": 4,
    "not_provided|CRYGA-related_disorder": 1,
    "Developmental_cataract|CRYGA-related_disorder": 1,
    "not_specified|Glioma_susceptibility_1": 2,
    "Maffucci_syndrome": 6,
    "Lymphoma": 3,
    "not_provided|IDH1-related_disorder": 3,
    "Enchondromatosis|Maffucci_syndrome": 2,
    "Enchondromatosis|not_specified": 1,
    "IDH1-related_disorder|not_specified|not_provided": 2,
    "not_provided|IDH1-related_disorder|not_specified": 1,
    "Metaphyseal_chondromatosis|Metaphyseal_chondromatosis_with_D-2-hydroxyglutaric_aciduria|Enchondromatosis|Glioblastoma_multiforme|_somatic|not_provided|Glioma_susceptibility_1": 1,
    "not_provided|Maffucci_syndrome|Enchondromatosis|Acute_myeloid_leukemia|Glioma_susceptibility_1": 1,
    "Glioma_susceptibility_1": 2,
    "Fleck_corneal_dystrophy": 122,
    "not_provided|Fleck_corneal_dystrophy": 26,
    "Inborn_genetic_diseases|Fleck_corneal_dystrophy": 6,
    "Fleck_corneal_dystrophy|not_provided": 22,
    "PIKFYVE-related_disorder|Inborn_genetic_diseases": 1,
    "PIKFYVE-related_disorder": 12,
    "Fleck_corneal_dystrophy|PIKFYVE-related_disorder|not_provided": 1,
    "PIKFYVE-related_disorder|Fleck_corneal_dystrophy|not_provided": 2,
    "not_provided|PIKFYVE-related_disorder": 2,
    "PIKFYVE-related_disorder|not_provided|Fleck_corneal_dystrophy": 2,
    "Inborn_genetic_diseases|PIKFYVE-related_disorder": 1,
    "PIKFYVE-related_disorder|Fleck_corneal_dystrophy": 1,
    "Fleck_corneal_dystrophy|Inborn_genetic_diseases": 3,
    "not_provided|Fleck_corneal_dystrophy|PIKFYVE-related_disorder": 1,
    "not_provided|PTH2R-related_disorder": 1,
    "PTH2R-related_disorder": 9,
    "not_specified|PTH2R-related_disorder": 2,
    "MAP2-associated_Neurodevelopmental_Disorder": 1,
    "Rett_syndrome": 413,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided": 29,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 57,
    "UNC80-related_disorder|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided": 3,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|Inborn_genetic_diseases": 2,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|UNC80-related_disorder|not_provided": 2,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided|Intellectual_disability": 1,
    "UNC80-related_disorder|not_provided": 21,
    "Encephalopathy|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "not_provided|UNC80-related_disorder": 32,
    "UNC80-related_disorder": 7,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 35,
    "UNC80-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided": 4,
    "UNC80-related_disorder|Inborn_genetic_diseases": 2,
    "UNC80-related_disorder|not_provided|Encephalopathy|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided|UNC80-related_disorder": 2,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_specified|not_provided": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|Inborn_genetic_diseases": 2,
    "not_provided|UNC80-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 3,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|UNC80-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Neurodevelopmental_delay|Intellectual_disability": 1,
    "not_provided|not_specified|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "not_provided|UNC80-related_disorder|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "Inborn_genetic_diseases|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 5,
    "Inborn_genetic_diseases|See_cases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 4,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|Encephalopathy": 1,
    "UNC80-related_disorder|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 3,
    "UNC80-related_disorder|not_specified|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|Inborn_genetic_diseases|not_provided": 1,
    "UNC80-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|See_cases": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|not_provided|Inborn_genetic_diseases": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|Inborn_genetic_diseases|not_provided": 4,
    "UNC80-related_disorder|not_provided|Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "UNC80-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2|Inborn_genetic_diseases|UNC80-related_disorder|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_2": 1,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1576,
    "ACADL-related_disorder": 14,
    "ACADL-related_disorder|not_provided": 2,
    "Long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "not_provided|Long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided|not_specified": 1,
    "not_specified|ACADL-related_disorder": 1,
    "Congenital_myopathy_with_reduced_type_2_muscle_fibers": 2,
    "MYL1-related_disorder": 5,
    "not_provided|MYL1-related_disorder": 1,
    "MYL1-related_disorder|not_provided|Congenital_myopathy_with_reduced_type_2_muscle_fibers": 1,
    "Congenital_hyperammonemia|_type_I": 1546,
    "not_specified|not_provided|Congenital_hyperammonemia|_type_I": 11,
    "Congenital_hyperammonemia|_type_I|not_provided": 21,
    "CPS1-related_disorder|Congenital_hyperammonemia|_type_I|not_specified|not_provided": 1,
    "not_provided|Congenital_hyperammonemia|_type_I|not_specified": 4,
    "CPS1-related_disorder|Congenital_hyperammonemia|_type_I": 5,
    "not_provided|Congenital_hyperammonemia|_type_I": 22,
    "Inborn_genetic_diseases|not_provided|Congenital_hyperammonemia|_type_I": 2,
    "Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to": 36,
    "Inborn_genetic_diseases|Congenital_hyperammonemia|_type_I": 22,
    "Congenital_hyperammonemia|_type_I|not_specified": 15,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to": 65,
    "Inborn_genetic_diseases|Congenital_hyperammonemia|_type_I|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_hyperammonemia|_type_I|not_specified": 1,
    "not_specified|Congenital_hyperammonemia|_type_I": 21,
    "CPS1-related_disorder": 2,
    "Congenital_hyperammonemia|_type_I|not_specified|Pulmonary_hypertension|_neonatal|_susceptibility_to": 2,
    "Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases": 30,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I": 31,
    "Congenital_hyperammonemia|_type_I|CPS1-related_disorder": 5,
    "Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases|CPS1-related_disorder|not_provided": 1,
    "not_provided|Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I": 2,
    "not_provided|Congenital_hyperammonemia|_type_I|CPS1-related_disorder": 1,
    "not_specified|not_provided|Congenital_hyperammonemia|_type_I|CPS1-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_provided": 1,
    "not_provided|not_specified|Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to": 1,
    "Congenital_hyperammonemia|_type_I|not_specified|not_provided": 5,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I|not_specified|not_provided": 2,
    "not_provided|not_specified|Congenital_hyperammonemia|_type_I": 2,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_specified|CPS1-related_disorder": 1,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|not_provided|Congenital_hyperammonemia|_type_I": 4,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_provided": 3,
    "not_specified|Pulmonary_hypertension|_neonatal|_susceptibility_to": 2,
    "not_specified|Pulmonary_hypertension|_neonatal|_susceptibility_to|Inborn_genetic_diseases|Congenital_hyperammonemia|_type_I": 1,
    "not_provided|Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to": 1,
    "not_specified|Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases": 2,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I|not_provided": 2,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|Inborn_genetic_diseases": 2,
    "CPS1-related_disorder|Congenital_hyperammonemia|_type_I|not_provided": 1,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|CPS1-related_disorder|Congenital_hyperammonemia|_type_I": 1,
    "CPS1-related_disorder|not_specified|not_provided|Congenital_hyperammonemia|_type_I": 2,
    "Congenital_hyperammonemia|_type_I|not_provided|CPS1-related_disorder": 2,
    "Neonatal_encephalopathy": 10,
    "not_specified|Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I": 2,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|CPS1-related_disorder|Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|CPS1-related_disorder|not_specified|Congenital_hyperammonemia|_type_I": 1,
    "not_provided|Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_specified": 1,
    "Congenital_hyperammonemia|_type_I|CPS1-related_disorder|not_specified": 1,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_provided|not_specified": 1,
    "not_provided|Congenital_hyperammonemia|_type_I|CPS1-related_disorder|not_specified": 1,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "CPS1-related_disorder|Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I|not_specified|not_provided": 1,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_specified": 1,
    "Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases|Pulmonary_hypertension|_neonatal|_susceptibility_to|CPS1-related_disorder": 1,
    "CPS1-related_disorder|not_provided|not_specified|Congenital_hyperammonemia|_type_I": 1,
    "not_specified|Congenital_hyperammonemia|_type_I|not_provided": 2,
    "Congenital_hyperammonemia|_type_I|CPS1-related_disorder|not_provided": 1,
    "Congenital_hyperammonemia|_type_I|not_provided|not_specified": 2,
    "not_provided|Congenital_hyperammonemia|_type_I|not_specified|Pulmonary_hypertension|_neonatal|_susceptibility_to": 1,
    "CPS1-related_disorder|Congenital_hyperammonemia|_type_I|Intellectual_disability": 1,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I|not_specified": 1,
    "not_specified|Congenital_hyperammonemia|_type_I|not_provided|Pulmonary_hypertension|_neonatal|_susceptibility_to": 1,
    "CPS1-related_disorder|not_provided|Congenital_hyperammonemia|_type_I": 1,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases": 1,
    "not_specified|Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_provided": 1,
    "not_provided|Congenital_hyperammonemia|_type_I|Inborn_genetic_diseases": 1,
    "CARBAMOYL_PHOSPHATE_SYNTHETASE_I_POLYMORPHISM|not_specified|not_provided|Congenital_hyperammonemia|_type_I": 1,
    "Pulmonary_hypertension|_neonatal|_susceptibility_to|not_specified|Congenital_hyperammonemia|_type_I": 1,
    "Congenital_hyperammonemia|_type_I|Pulmonary_hypertension|_neonatal|_susceptibility_to|not_provided|CPS1-related_disorder": 1,
    "ERBB4-related_disorder|not_provided": 24,
    "Amyotrophic_lateral_sclerosis_type_19|not_provided": 7,
    "Amyotrophic_lateral_sclerosis_type_19": 12,
    "ERBB4-related_disorder": 26,
    "not_provided|ERBB4-related_disorder": 25,
    "Frontotemporal_dementia|not_provided": 15,
    "ERBB4-related_disorder|Amyotrophic_lateral_sclerosis_type_19|not_provided": 1,
    "not_provided|not_specified|ERBB4-related_disorder": 2,
    "ERBB4-related_Non-syndromic_intellectual_disability_or_epilepsy": 1,
    "ERBB4-related_disorder|Amyotrophic_lateral_sclerosis_type_19|not_specified|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_19": 3,
    "not_provided|ERBB4-related_disorder|Inborn_genetic_diseases": 1,
    "ERBB4-associated_epilepsy_syndrome": 1,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_19": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_10": 1,
    "not_specified|ERBB4-related_disorder|not_provided": 1,
    "ERBB4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "ERBB4-related_disorder|Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_19|not_provided": 1,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_19": 1,
    "ERBB4-related_disorder|not_specified|not_provided": 1,
    "NK-cell_enteropathy": 10,
    "Amyotrophic_lateral_sclerosis_type_19|Inborn_genetic_diseases": 1,
    "ERBB4-related_disorder|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "not_specified|ICHAD_SYNDROME": 1,
    "SPAG16-related_disorder": 1,
    "not_provided|Familial_cancer_of_breast": 124,
    "BARD1-related_cancer_predisposition": 7,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2372,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 47,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2089,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 167,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 9,
    "not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 17,
    "BARD1-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 150,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 83,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 292,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 6,
    "BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 161,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 122,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 48,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 177,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 45,
    "not_specified|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "BARD1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided": 5,
    "Familial_cancer_of_breast|BARD1-related_disorder": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 4,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 33,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|not_specified|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 6,
    "Ovarian_cancer|Familial_cancer_of_breast|BARD1-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 27,
    "not_provided|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 9,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast": 6,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 3,
    "not_provided|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 54,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 11,
    "Familial_cancer_of_breast|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|BARD1-related_disorder": 2,
    "not_provided|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 5,
    "not_specified|Familial_cancer_of_breast|not_provided|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|BARD1-related_cancer_predisposition|not_specified": 1,
    "Familial_adenomatous_polyposis_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_specified|BARD1-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 40,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_cancer_predisposition": 3,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|BARD1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "not_provided|BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition": 1,
    "BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Familial_cancer_of_breast|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified": 9,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 11,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition": 2,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_cancer|Familial_cancer_of_breast": 1,
    "BARD1-related_cancer_predisposition|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 15,
    "BARD1-related_cancer_predisposition|Familial_cancer_of_breast": 3,
    "BARD1-related_disorder|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer|BARD1-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Triple-Negative_Breast_Cancer_Finding|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition": 1,
    "Gastric_cancer|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "BARD1-related_cancer_predisposition|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Triple-Negative_Breast_Cancer_Finding": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_provided": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 3,
    "BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Gastric_cancer": 11,
    "BARD1-related_disorder|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Familial_ovarian_cancer|not_provided|not_specified": 1,
    "not_provided|BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|Familial_cancer_of_breast": 1,
    "not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_provided|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 4,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "not_specified|Familial_cancer_of_breast|BARD1-related_cancer_predisposition|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_disorder": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Familial_cancer_of_breast|not_specified|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|not_specified|Familial_cancer_of_breast|not_provided": 2,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 8,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 9,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|not_provided|Familial_cancer_of_breast": 1,
    "BARD1-related_cancer_predisposition|BARD1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma|Familial_cancer_of_breast|Triple-Negative_Breast_Cancer_Finding": 1,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "BARD1-related_cancer_predisposition|not_provided|not_specified|Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast_cancer|_susceptibility_to|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 20,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified": 2,
    "BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_cancer|_susceptibility_to": 1,
    "not_specified|Familial_cancer_of_breast|not_provided": 2,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 55,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "BARD1-related_cancer_predisposition|not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BARD1-related_cancer_predisposition|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 32,
    "Familial_cancer_of_breast|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|Ovarian_cancer|not_provided|Familial_cancer_of_breast": 1,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|BARD1-related_cancer_predisposition|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 38,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 7,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 180,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Familial_cancer_of_breast|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 3,
    "BARD1-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BARD1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|not_specified|BARD1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "BARD1-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BARD1-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|not_provided|BARD1-related_disorder|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|BARD1-related_cancer_predisposition|Breast_neoplasm|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|Familial_cancer_of_breast": 2,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "BARD1-related_disorder|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 6,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 3,
    "Breast_and/or_ovarian_cancer|Familial_ovarian_cancer|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Triple-Negative_Breast_Cancer_Finding": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BARD1-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 8,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 4,
    "not_provided|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_cancer_predisposition|not_provided|not_specified": 1,
    "Familial_cancer_of_breast|BARD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hepatoblastoma|not_provided": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder": 1,
    "not_provided|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|BARD1-related_cancer_predisposition|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "BARD1-related_cancer_predisposition|BARD1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 26,
    "Carcinoma_of_colon|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lung_cancer|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 9,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 23,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 3,
    "not_specified|Familial_cancer_of_breast|Triple-Negative_Breast_Cancer_Finding|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Familial_ovarian_cancer": 1,
    "BARD1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition": 1,
    "BARD1-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|not_specified|BARD1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "BARD1-related_disorder|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|BARD1-related_cancer_predisposition": 1,
    "Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 4,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|BARD1-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|BARD1-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|BARD1-related_cancer_predisposition|BARD1-related_disorder|Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|BARD1-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|BARD1-related_cancer_predisposition|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "BARD1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|BARD1-related_disorder": 1,
    "BARD1-related_cancer_predisposition|BARD1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Breast_neoplasm": 1,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "BARD1-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_thyroid_gland|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 4,
    "not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Breast_and/or_ovarian_cancer|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_disorder|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|not_specified|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|BARD1-related_disorder": 1,
    "not_provided|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|BARD1-related_disorder": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 2,
    "BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 6,
    "Gastric_cancer|BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer": 1,
    "Familial_cancer_of_breast|not_specified|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast": 2,
    "BARD1-related_disorder|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_disorder|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|BARD1-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|BARD1-related_disorder|Familial_cancer_of_breast": 1,
    "Breast_neoplasm|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 18,
    "Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "BARD1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 3,
    "BARD1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|BARD1-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "BARD1-related_disorder|BARD1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BARD1-related_cancer_predisposition": 1,
    "BARD1-related_cancer_predisposition|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BARD1-related_disorder|not_specified|Familial_cancer_of_breast": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "BARD1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 2,
    "BARD1-related_cancer_predisposition|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BARD1-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|Ovarian_cancer|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|BARD1-related_disorder|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "BARD1-related_disorder|Hereditary_cancer-predisposing_syndrome|BARD1-related_cancer_predisposition|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|BARD1-related_disorder": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BARD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Congenital_ichthyosiform_erythroderma": 28,
    "Congenital_ichthyosis_of_skin": 56,
    "Congenital_ichthyosis_of_skin|not_provided": 29,
    "Congenital_ichthyosis_of_skin|not_provided|Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B": 13,
    "Autosomal_recessive_congenital_ichthyosis_4B|ABCA12-related_disorder|not_provided|Inborn_genetic_diseases|Congenital_ichthyosis_of_skin": 1,
    "Autosomal_recessive_congenital_ichthyosis_4B": 24,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "ABCA12-related_disorder": 12,
    "not_provided|Congenital_ichthyosis_of_skin": 25,
    "Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A|not_provided": 5,
    "Autosomal_recessive_congenital_ichthyosis_4B|Lamellar_ichthyosis|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B|not_provided": 9,
    "Autosomal_recessive_congenital_ichthyosis_4B|not_provided": 4,
    "Autosomal_recessive_congenital_ichthyosis_4A": 12,
    "Congenital_ichthyosiform_erythroderma|not_provided": 4,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A|Congenital_ichthyosis_of_skin|not_provided|not_specified": 1,
    "Congenital_ichthyosis_of_skin|not_specified|not_provided": 1,
    "ABCA12-related_disorder|not_provided|Congenital_ichthyosis_of_skin": 6,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "Lamellar_ichthyosis": 23,
    "Congenital_ichthyosis_of_skin|not_provided|ABCA12-related_disorder": 1,
    "Congenital_ichthyosis_of_skin|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|ABCA12-related_disorder": 11,
    "not_specified|not_provided|Congenital_ichthyosis_of_skin": 3,
    "Inborn_genetic_diseases|Congenital_ichthyosis_of_skin|not_provided": 3,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_4B|Congenital_ichthyosis_of_skin|Autosomal_recessive_congenital_ichthyosis_4A": 3,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "ABCA12-related_disorder|Congenital_ichthyosis_of_skin|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "not_provided|ABCA12-related_disorder|Congenital_ichthyosis_of_skin": 3,
    "Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A": 3,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A": 7,
    "Autosomal_recessive_congenital_ichthyosis_4B|not_provided|Autosomal_recessive_congenital_ichthyosis_4A": 2,
    "ABCA12-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|Congenital_ichthyosis_of_skin|not_provided|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "not_provided|Congenital_ichthyosis_of_skin|not_specified": 1,
    "Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B|Congenital_ichthyosis_of_skin|not_provided": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_4A|not_specified": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B": 3,
    "Congenital_ichthyosis_of_skin|ABCA12-related_disorder|not_provided": 3,
    "ABCA12-related_disorder|Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "Autosomal_recessive_congenital_ichthyosis_4A|Lamellar_ichthyosis|not_provided": 1,
    "not_provided|Congenital_ichthyosis_of_skin|ABCA12-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_ichthyosis_of_skin": 1,
    "Autosomal_recessive_congenital_ichthyosis_4B|Inborn_genetic_diseases": 1,
    "Congenital_ichthyosis_of_skin|not_provided|Autosomal_recessive_congenital_ichthyosis_4B|not_specified": 1,
    "Inborn_genetic_diseases|Congenital_ichthyosis_of_skin": 5,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A|not_specified": 1,
    "not_specified|Congenital_ichthyosis_of_skin|not_provided|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "Autosomal_recessive_congenital_ichthyosis_4A|Inborn_genetic_diseases": 1,
    "Lamellar_ichthyosis|not_provided": 4,
    "Ichthyosis": 5,
    "Abnormality_of_the_skin|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "not_specified|not_provided|Congenital_ichthyosis_of_skin|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "ABCA12-related_disorder|Congenital_ichthyosis_of_skin|not_specified|Autosomal_recessive_congenital_ichthyosis_4A|Autosomal_recessive_congenital_ichthyosis_4B|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_4A|not_provided": 2,
    "Congenital_ichthyosis_of_skin|not_provided|not_specified": 2,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A|Congenital_ichthyosis_of_skin": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_4A": 1,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_4B|Autosomal_recessive_congenital_ichthyosis_4A|not_provided": 1,
    "not_provided|Lamellar_ichthyosis": 3,
    "ABCA12-related_disorder|Congenital_ichthyosis_of_skin|not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_4B": 1,
    "not_provided|Congenital_ichthyosis_of_skin|Inborn_genetic_diseases": 1,
    "AICA-ribosiduria|not_provided": 10,
    "not_provided|AICA-ribosiduria|Intellectual_disability": 1,
    "AICA-ribosiduria": 9,
    "ATIC-related_disorder": 2,
    "ATIC-related_disorder|not_provided": 2,
    "not_provided|AICA-ribosiduria|ATIC-related_disorder": 1,
    "not_provided|ATIC-related_disorder": 4,
    "not_provided|not_specified|AICA-ribosiduria": 1,
    "AICA-ribosiduria|See_cases|not_provided": 1,
    "not_provided|AICA-ribosiduria": 1,
    "not_provided|methotrexate_response_-_Efficacy": 1,
    "AICA-ribosiduria|not_specified|not_provided": 1,
    "not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2": 22,
    "not_provided|Chronic_kidney_disease|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2": 2,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|not_provided": 28,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|Inborn_genetic_diseases": 2,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 153,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided": 57,
    "not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 50,
    "FN1-related_disorder|not_provided": 15,
    "Glomerulopathy_with_fibronectin_deposits_2": 23,
    "not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Inborn_genetic_diseases": 6,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Inborn_genetic_diseases|not_provided": 13,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Inborn_genetic_diseases|Birt-Hogg-Dube_syndrome_1": 1,
    "Glomerulopathy_with_fibronectin_deposits_2|not_provided": 2,
    "not_provided|FN1-related_disorder": 7,
    "not_specified|Glomerulopathy_with_fibronectin_deposits_2|not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 1,
    "FN1-related_disorder|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided": 1,
    "FN1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 10,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided|Inborn_genetic_diseases": 3,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Glomerulopathy_with_fibronectin_deposits_2": 4,
    "Inborn_genetic_diseases|not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2": 1,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|FN1-related_disorder|not_provided": 3,
    "FN1-related_disorder": 11,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided|FN1-related_disorder": 3,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided|not_specified": 3,
    "not_provided|Chronic_kidney_disease": 1,
    "Inborn_genetic_diseases|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 5,
    "Glomerulopathy_with_fibronectin_deposits_2|Plasma_fibronectin_deficiency|not_provided": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided|Glomerulopathy_with_fibronectin_deposits_2": 1,
    "not_provided|Inborn_genetic_diseases|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 3,
    "FN1-related_disorder|not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 2,
    "not_provided|Inborn_genetic_diseases|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2": 2,
    "not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 2,
    "Inborn_genetic_diseases|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided": 5,
    "Glomerulopathy_with_fibronectin_deposits_2|not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 4,
    "not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Inborn_genetic_diseases": 1,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Inborn_genetic_diseases": 5,
    "not_specified|Chronic_kidney_disease|not_provided": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 13,
    "FN1-related_disorder|Inborn_genetic_diseases": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|Inborn_genetic_diseases|not_provided": 2,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|FN1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_1|Glomerulopathy_with_fibronectin_deposits_2|not_provided": 1,
    "Glomerulopathy_with_fibronectin_deposits_2|FN1-related_disorder": 1,
    "Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|FN1-related_disorder": 1,
    "not_provided|FN1-related_disorder|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 1,
    "Inborn_genetic_diseases|Glomerulopathy_with_fibronectin_deposits_2|not_provided": 1,
    "Inborn_genetic_diseases|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|not_provided": 1,
    "FN1-related_disorder|Inborn_genetic_diseases|not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondylometaphyseal_dysplasia": 4,
    "not_specified|not_provided|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|not_provided|FN1-related_disorder": 2,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Glomerulopathy_with_fibronectin_deposits_2|Inborn_genetic_diseases|not_provided|FN1-related_disorder": 1,
    "not_provided|X-linked_Alport_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|Spondylometaphyseal_dysplasia": 4,
    "Spondylometaphyseal_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided": 1,
    "Spondylometaphyseal_dysplasia": 2,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Neurodevelopmental_disorder|not_provided|Spondylometaphyseal_dysplasia": 1,
    "Inborn_genetic_diseases|not_provided|FN1-related_disorder": 1,
    "Inborn_genetic_diseases|FN1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Glomerulopathy_with_fibronectin_deposits_2": 1,
    "not_specified|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided|Glomerulopathy_with_fibronectin_deposits_2": 2,
    "not_provided|Glomerulopathy_with_fibronectin_deposits_2|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_specified|Spondyloepimetaphyseal_dysplasia|_Strudwick_type": 1,
    "MREG-related_condition": 1,
    "Schimke_immuno-osseous_dysplasia": 1005,
    "not_provided|Schimke_immuno-osseous_dysplasia": 19,
    "Schimke_immuno-osseous_dysplasia|not_provided": 15,
    "SMARCAL1-related_disorder": 3,
    "Inborn_genetic_diseases|Schimke_immuno-osseous_dysplasia": 30,
    "Kidney_disorder|Schimke_immuno-osseous_dysplasia": 1,
    "Schimke_immuno-osseous_dysplasia|Inborn_genetic_diseases": 19,
    "Schimke_immuno-osseous_dysplasia|SMARCAL1-related_disorder": 8,
    "Schimke_immuno-osseous_dysplasia|not_specified|not_provided": 2,
    "not_provided|SMARCAL1-related_disorder|Schimke_immuno-osseous_dysplasia": 2,
    "Schimke_immuno-osseous_dysplasia|Inborn_genetic_diseases|SMARCAL1-related_disorder": 1,
    "not_specified|not_provided|Kidney_disorder|Schimke_immuno-osseous_dysplasia": 1,
    "Focal_segmental_glomerulosclerosis|Schimke_immuno-osseous_dysplasia": 2,
    "not_specified|Schimke_immuno-osseous_dysplasia|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "Schimke_immuno-osseous_dysplasia|Microcephaly|Familial_atrioventricular_septal_defect|Small_for_gestational_age|Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Short_stature|Primary_microcephaly|Disproportionate_short-trunk_short_stature|Decreased_body_weight": 1,
    "Schimke_immuno-osseous_dysplasia|not_specified": 2,
    "SMARCAL1-related_disorder|Schimke_immuno-osseous_dysplasia|not_provided": 3,
    "not_provided|Schimke_immuno-osseous_dysplasia|SMARCAL1-related_disorder": 3,
    "Schimke_immuno-osseous_dysplasia|not_provided|Inborn_genetic_diseases": 1,
    "Schimke_immuno-osseous_dysplasia|not_provided|not_specified": 3,
    "not_specified|Schimke_immuno-osseous_dysplasia|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Schimke_immuno-osseous_dysplasia|not_provided|Kidney_disorder|not_specified": 1,
    "Schimke_immuno-osseous_dysplasia|not_provided|Inborn_genetic_diseases|SMARCAL1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Schimke_immuno-osseous_dysplasia": 1,
    "SMARCAL1-related_disorder|Schimke_immuno-osseous_dysplasia": 6,
    "not_provided|not_specified|Schimke_immuno-osseous_dysplasia|Focal_segmental_glomerulosclerosis": 1,
    "Schimke_immuno-osseous_dysplasia|Inherited_Immunodeficiency_Diseases": 1,
    "Schimke_immuno-osseous_dysplasia|See_cases": 1,
    "See_cases|SMARCAL1-related_disorder|not_provided|Schimke_immuno-osseous_dysplasia": 1,
    "SMARCAL1-related_disorder|not_provided|Schimke_immuno-osseous_dysplasia": 1,
    "Schimke_immuno-osseous_dysplasia|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Kidney_disorder|SMARCAL1-related_disorder|not_specified|not_provided|Schimke_immuno-osseous_dysplasia": 1,
    "See_cases|Schimke_immuno-osseous_dysplasia": 1,
    "not_provided|Kidney_disorder|Schimke_immuno-osseous_dysplasia": 1,
    "not_provided|Inborn_genetic_diseases|Schimke_immuno-osseous_dysplasia": 2,
    "Nephrotic_syndrome|Schimke_immuno-osseous_dysplasia": 1,
    "Schimke_immuno-osseous_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Schimke_immuno-osseous_dysplasia|Inborn_genetic_diseases": 1,
    "Schimke_immuno-osseous_dysplasia|Focal_segmental_glomerulosclerosis": 1,
    "SMARCAL1-related_disorder|Inborn_genetic_diseases|not_provided|Schimke_immuno-osseous_dysplasia": 1,
    "Schimke_immuno-osseous_dysplasia|Nephrotic_syndrome": 2,
    "Schimke_immuno-osseous_dysplasia|not_provided|not_specified|Focal_segmental_glomerulosclerosis": 1,
    "Atypical_hemolytic-uremic_syndrome|Schimke_immuno-osseous_dysplasia": 1,
    "not_specified|Schimke_immuno-osseous_dysplasia|not_provided": 1,
    "Schimke_immuno-osseous_dysplasia|SMARCAL1-related_disorder|Inherited_Immunodeficiency_Diseases|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Schimke_immuno-osseous_dysplasia|Kidney_disorder": 1,
    "not_specified|Schimke_immuno-osseous_dysplasia": 1,
    "Schimke_immuno-osseous_dysplasia|not_provided|Inherited_Immunodeficiency_Diseases": 1,
    "Schimke_immuno-osseous_dysplasia|Focal_segmental_glomerulosclerosis|not_provided|SMARCAL1-related_disorder": 1,
    "Nephrotic_syndrome|not_provided|Schimke_immuno-osseous_dysplasia|Small_for_gestational_age|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome|Primary_microcephaly|Microcephaly|Decreased_body_weight|Disproportionate_short-trunk_short_stature|Familial_atrioventricular_septal_defect|Short_stature": 1,
    "Inborn_genetic_diseases|Schimke_immuno-osseous_dysplasia|not_provided": 1,
    "Schimke_immuno-osseous_dysplasia|SMARCAL1-related_disorder|not_provided": 1,
    "TNS1-related_disorder": 57,
    "TNS1-related_disorder|not_specified": 1,
    "TNS1-related_disorder|not_provided": 9,
    "not_provided|TNS1-related_disorder": 7,
    "not_specified|TNS1-related_disorder": 1,
    "not_provided|CXCR2-related_disorder": 3,
    "CXCR2-related_disorder|not_provided": 3,
    "WHIM_syndrome_2": 2,
    "CXCR2-related_disorder": 1,
    "CXCR1-related_disorder|not_provided": 1,
    "CXCR1-related_disorder": 3,
    "CXCR1-related_disorder|Cholangiocarcinoma": 1,
    "not_provided|CXCR1-related_disorder": 1,
    "not_provided|Susceptibility_to_HIV_infection": 1,
    "GPBAR1-related_disorder|not_provided": 11,
    "GPBAR1-related_disorder": 31,
    "GPBAR1-related_disorder|not_specified": 6,
    "not_specified|GPBAR1-related_disorder": 3,
    "not_provided|GPBAR1-related_disorder": 8,
    "GPBAR1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|GPBAR1-related_disorder": 4,
    "not_provided|GPBAR1-related_disorder|not_specified": 1,
    "GPBAR1-related_disorder|not_specified|not_provided": 1,
    "not_specified|GPBAR1-related_disorder|not_provided": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia_1|not_provided": 7,
    "Paroxysmal_nonkinesigenic_dyskinesia_1": 41,
    "Paroxysmal_nonkinesigenic_dyskinesia": 377,
    "not_provided|Paroxysmal_nonkinesigenic_dyskinesia": 8,
    "Paroxysmal_nonkinesigenic_dyskinesia_1|Paroxysmal_nonkinesigenic_dyskinesia": 10,
    "Paroxysmal_nonkinesigenic_dyskinesia|Paroxysmal_nonkinesigenic_dyskinesia_1|PNKD-related_disorder|not_provided": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1|Paroxysmal_dyskinesia|Paroxysmal_dystonia|Episodic_hemiplegia": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_specified": 5,
    "Paroxysmal_nonkinesigenic_dyskinesia|Paroxysmal_nonkinesigenic_dyskinesia_1": 9,
    "Paroxysmal_nonkinesigenic_dyskinesia|Inborn_genetic_diseases": 14,
    "Inborn_genetic_diseases|Paroxysmal_nonkinesigenic_dyskinesia": 12,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1": 3,
    "Inborn_genetic_diseases|Paroxysmal_nonkinesigenic_dyskinesia|not_specified": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_provided": 9,
    "PNKD-related_disorder": 5,
    "not_provided|PNKD-related_disorder": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|PNKD-related_disorder|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia_1|Paroxysmal_nonkinesigenic_dyskinesia|not_provided|PNKD-related_disorder": 3,
    "Paroxysmal_nonkinesigenic_dyskinesia|Paroxysmal_nonkinesigenic_dyskinesia_1|not_provided|PNKD-related_disorder": 1,
    "not_provided|Paroxysmal_nonkinesigenic_dyskinesia|not_specified|Paroxysmal_nonkinesigenic_dyskinesia_1": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|Inborn_genetic_diseases|Paroxysmal_nonkinesigenic_dyskinesia_1": 2,
    "PNKD-related_disorder|Paroxysmal_nonkinesigenic_dyskinesia": 3,
    "not_provided|Paroxysmal_nonkinesigenic_dyskinesia|Inborn_genetic_diseases": 3,
    "Paroxysmal_nonkinesigenic_dyskinesia|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Paroxysmal_nonkinesigenic_dyskinesia": 3,
    "Inborn_genetic_diseases|Paroxysmal_nonkinesigenic_dyskinesia|not_provided": 2,
    "not_specified|PNKD-related_disorder|Paroxysmal_nonkinesigenic_dyskinesia|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1": 1,
    "not_provided|Paroxysmal_nonkinesigenic_dyskinesia|Paroxysmal_nonkinesigenic_dyskinesia_1": 2,
    "Paroxysmal_nonkinesigenic_dyskinesia|Young-onset_Parkinson_disease|Paroxysmal_nonkinesigenic_dyskinesia_1|not_provided": 1,
    "not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1": 5,
    "Paroxysmal_nonkinesigenic_dyskinesia_1|not_specified|not_provided|Paroxysmal_nonkinesigenic_dyskinesia": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_specified|not_provided": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_specified|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|Paroxysmal_nonkinesigenic_dyskinesia_1|not_provided": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1|not_specified": 1,
    "PNKD-related_disorder|not_provided|Paroxysmal_nonkinesigenic_dyskinesia": 1,
    "PNKD-related_disorder|Paroxysmal_nonkinesigenic_dyskinesia|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1": 1,
    "Paroxysmal_nonkinesigenic_dyskinesia_1|Paroxysmal_nonkinesigenic_dyskinesia|not_provided": 1,
    "Inborn_genetic_diseases|Paroxysmal_nonkinesigenic_dyskinesia|Paroxysmal_nonkinesigenic_dyskinesia_1": 1,
    "Inborn_genetic_diseases|Paroxysmal_nonkinesigenic_dyskinesia|not_provided|not_specified": 1,
    "not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1|Paroxysmal_nonkinesigenic_dyskinesia": 1,
    "Spermatogenic_failure_54": 1,
    "SLC11A1-related_disorder": 8,
    "Mycobacterium_tuberculosis|_susceptibility_to_infection_by": 1,
    "not_provided|SLC11A1-related_disorder": 1,
    "Buruli_ulcer|_susceptibility_to|Cystic_fibrosis": 1,
    "VIL1-related_disorder": 12,
    "not_provided|VIL1-related_disorder": 1,
    "VIL1-related_disorder|not_provided": 1,
    "CNOT9-associated_neurodevelopmental_disorder": 2,
    "not_provided|CNOT9-associated_neurodevelopmental_disorder": 1,
    "See_cases|CNOT9-associated_neurodevelopmental_disorder|not_provided": 1,
    "ZNF142-related_disorder|not_provided": 11,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements": 6,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements": 46,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements|Inborn_genetic_diseases": 5,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements|ZNF142-related_disorder|not_provided": 2,
    "not_specified|ZNF142-related_disorder|Inborn_genetic_diseases": 1,
    "ZNF142-related_disorder": 10,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements|not_provided": 4,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements|Intellectual_disability|Seizure": 1,
    "not_provided|ZNF142-related_disorder": 5,
    "Inborn_genetic_diseases|ZNF142-related_disorder|not_provided": 2,
    "ZNF142-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements": 4,
    "ZNF142-related_disorder|not_provided|Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements": 2,
    "ZNF142-related_disorder|not_specified": 1,
    "Neurodevelopmental_disorder_with_impaired_speech_and_hyperkinetic_movements|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Leigh_syndrome": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|Leigh_syndrome|GRACILE_syndrome": 2,
    "GRACILE_syndrome|Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 28,
    "GRACILE_syndrome": 33,
    "not_specified|Pili_torti-deafness_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|not_provided|BCS1L-related_disorder": 1,
    "Leigh_syndrome|GRACILE_syndrome|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "GRACILE_syndrome|not_provided": 11,
    "not_provided|GRACILE_syndrome": 9,
    "GRACILE_syndrome|not_provided|not_specified": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|not_specified|GRACILE_syndrome|Leigh_syndrome": 1,
    "Leigh_syndrome|not_specified|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "GRACILE_syndrome|Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|not_provided": 4,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1": 26,
    "not_provided|Pili_torti-deafness_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 2,
    "BJORNSTAD_SYNDROME_WITH_MILD_MITOCHONDRIAL_COMPLEX_III_DEFICIENCY": 1,
    "Leigh_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "not_specified|not_provided|Leigh_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome|not_provided": 2,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Pili_torti-deafness_syndrome": 3,
    "BCS1L-related_disorder|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Pili_torti-deafness_syndrome|Leigh_syndrome|not_provided": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome": 3,
    "Leigh_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|BCS1L-related_disorder|GRACILE_syndrome|not_provided|not_specified": 1,
    "Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome": 3,
    "GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|not_provided|not_specified": 1,
    "not_provided|Leigh_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 3,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome": 1,
    "not_provided|GRACILE_syndrome|Pili_torti-deafness_syndrome": 5,
    "BCS1L-related_disorder|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Pili_torti-deafness_syndrome|not_provided": 1,
    "not_provided|GRACILE_syndrome|Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 4,
    "Leigh_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|not_provided|GRACILE_syndrome": 1,
    "Pili_torti-deafness_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 3,
    "Movement_disorder|Microcephaly|Sparse_hair|Pili_torti-deafness_syndrome|Intellectual_disability|_severe|not_provided|Intellectual_disability": 1,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1": 3,
    "not_provided|Pili_torti-deafness_syndrome": 3,
    "GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome": 5,
    "Inborn_genetic_diseases|not_provided|GRACILE_syndrome|Pili_torti-deafness_syndrome": 1,
    "Pili_torti-deafness_syndrome|Neonatal_encephalopathy": 1,
    "Pili_torti-deafness_syndrome|GRACILE_syndrome|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "Pili_torti-deafness_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|not_provided": 7,
    "not_provided|Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome": 1,
    "Pili_torti-deafness_syndrome": 13,
    "Pili_torti-deafness_syndrome|not_provided|GRACILE_syndrome|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|GRACILE_syndrome": 1,
    "Pili_torti-deafness_syndrome|not_provided|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome": 1,
    "Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|not_specified|not_provided": 1,
    "Decreased_activity_of_mitochondrial_complex_III": 1,
    "not_provided|BCS1L-related_disorder": 1,
    "Pili_torti-deafness_syndrome|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome": 1,
    "GRACILE_syndrome|not_provided|Inborn_genetic_diseases|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome": 1,
    "Movement_disorder|Microcephaly|Sparse_hair|Pili_torti-deafness_syndrome|Intellectual_disability|_severe|not_provided|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Intellectual_disability": 1,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Pili_torti-deafness_syndrome|not_provided": 5,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome": 1,
    "BCS1L-related_disorder|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Pili_torti-deafness_syndrome|not_provided|BJORNSTAD_SYNDROME_WITH_MILD_MITOCHONDRIAL_COMPLEX_III_DEFICIENCY": 1,
    "GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|not_specified|not_provided|Leigh_syndrome|BCS1L-related_disorder": 1,
    "GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|not_provided|Pili_torti-deafness_syndrome|not_specified|Leigh_syndrome": 1,
    "Pili_torti-deafness_syndrome|not_provided|Inborn_genetic_diseases|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome": 1,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|GRACILE_syndrome|not_specified": 1,
    "not_specified|GRACILE_syndrome|Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|not_provided": 1,
    "Leigh_syndrome|not_provided|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "not_specified|Leigh_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|BCS1L-related_disorder|not_provided": 1,
    "not_provided|BCS1L-related_disorder|GRACILE_syndrome|not_specified": 1,
    "BCS1L-related_disorder|not_provided": 3,
    "Seizure|Severe_global_developmental_delay": 2,
    "GRACILE_syndrome|Pili_torti-deafness_syndrome|not_provided": 1,
    "Leigh_syndrome|not_specified|BCS1L-related_disorder|not_provided|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "not_provided|Neuromuscular_disease": 1,
    "BCS1L-related_disorder": 3,
    "Pili_torti-deafness_syndrome|not_provided": 1,
    "BCS1L-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|not_provided": 1,
    "GRACILE_syndrome|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome": 1,
    "GRACILE_syndrome|not_provided|Pili_torti-deafness_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|GRACILE_syndrome|Pili_torti-deafness_syndrome|not_provided|not_specified|Leigh_syndrome": 1,
    "Leigh_syndrome|not_specified|not_provided|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "not_provided|not_specified|Pili_torti-deafness_syndrome|GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1": 1,
    "GRACILE_syndrome|Mitochondrial_complex_III_deficiency_nuclear_type_1|Pili_torti-deafness_syndrome|Leigh_syndrome|not_provided|not_specified": 1,
    "Pili_torti-deafness_syndrome|BCS1L-related_disorder": 1,
    "Decreased_activity_of_mitochondrial_complex_III|GRACILE_syndrome": 1,
    "not_specified|STK36-related_disorder": 2,
    "Ciliary_dyskinesia|_primary|_46|not_provided|See_cases": 1,
    "STK36-related_disorder": 17,
    "not_specified|Ciliary_dyskinesia|_primary|_46": 1,
    "Ciliary_dyskinesia|_primary|_46|STK36-related_disorder": 1,
    "STK36-related_disorder|not_provided": 6,
    "not_provided|not_specified|STK36-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_46": 5,
    "not_provided|STK36-related_disorder": 4,
    "Spermatogenic_failure_18": 14,
    "Ciliary_dyskinesia|_primary|_46|not_provided|STK36-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_46|STK36-related_disorder|not_provided": 1,
    "STK36-related_disorder|Ciliary_dyskinesia|_primary|_46|not_provided": 1,
    "Cholestanol_storage_disease": 745,
    "Cholestanol_storage_disease|not_provided": 29,
    "not_specified|Cholestanol_storage_disease|not_provided": 1,
    "CYP27A1-related_disorder|Cholestanol_storage_disease|not_specified|not_provided": 1,
    "not_provided|Cholestanol_storage_disease": 33,
    "Cardiovascular_phenotype|Cholestanol_storage_disease": 55,
    "Cholestanol_storage_disease|Cardiovascular_phenotype": 42,
    "not_specified|Cardiovascular_phenotype|Cholestanol_storage_disease|CYP27A1-related_disorder": 1,
    "CYP27A1-related_disorder|Cardiovascular_phenotype|Cholestanol_storage_disease": 1,
    "Cardiovascular_phenotype|not_provided|Cholestanol_storage_disease": 16,
    "not_specified|Cardiovascular_phenotype|not_provided|Cholestanol_storage_disease": 1,
    "Cholestanol_storage_disease|Intellectual_disability|Cardiovascular_phenotype|not_provided": 1,
    "CYP27A1-related_disorder|Cholestanol_storage_disease|not_provided": 2,
    "Cardiovascular_phenotype|Cholestanol_storage_disease|not_provided": 10,
    "Cardiovascular_phenotype|CYP27A1-related_disorder|not_provided|Cholestanol_storage_disease": 2,
    "Cholestanol_storage_disease|Cardiovascular_phenotype|not_provided": 6,
    "not_provided|not_specified|Cholestanol_storage_disease": 2,
    "Cholestanol_storage_disease|not_provided|CYP27A1-related_disorder": 2,
    "not_provided|Cardiovascular_phenotype|Cholestanol_storage_disease": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|Cholestanol_storage_disease": 4,
    "CYP27A1-related_disorder|not_provided|Cholestanol_storage_disease": 9,
    "not_provided|CYP27A1-related_disorder|Cholestanol_storage_disease": 3,
    "not_specified|not_provided|Cholestanol_storage_disease|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cholestanol_storage_disease": 1,
    "CYP27A1-related_disorder|Cardiovascular_phenotype|Cholestanol_storage_disease|not_provided": 2,
    "Cardiovascular_phenotype|CYP27A1-related_disorder|Cholestanol_storage_disease": 2,
    "Premature_coronary_artery_atherosclerosis|Cholestanol_storage_disease": 1,
    "CYP27A1-related_disorder|not_provided|Cholestanol_storage_disease|See_cases": 1,
    "not_provided|Cholestanol_storage_disease|CYP27A1-related_disorder": 2,
    "Cardiovascular_phenotype|not_provided|Cholestanol_storage_disease|CYP27A1-related_disorder": 2,
    "Cardiovascular_phenotype|Cholestanol_storage_disease|CYP27A1-related_disorder": 2,
    "not_specified|Cholestanol_storage_disease": 3,
    "Cholestanol_storage_disease|CYP27A1-related_disorder|not_provided": 2,
    "Cholestanol_storage_disease|not_provided|Cardiovascular_phenotype": 4,
    "CYP27A1-related_disorder|Cardiovascular_phenotype|not_provided|Cholestanol_storage_disease": 9,
    "not_specified|not_provided|Cholestanol_storage_disease": 4,
    "Cholestanol_storage_disease|CYP27A1-related_disorder": 6,
    "not_provided|Cholestanol_storage_disease|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|CYP27A1-related_disorder|not_provided|Cholestanol_storage_disease|Intellectual_disability": 1,
    "CYP27A1-related_disorder|Cholestanol_storage_disease|not_provided|Cardiovascular_phenotype": 1,
    "CYP27A1-related_disorder|Cholestanol_storage_disease|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cholestanol_storage_disease|not_specified": 1,
    "Cholestanol_storage_disease|not_specified": 2,
    "Cardiovascular_phenotype|Cholestanol_storage_disease|not_specified|not_provided": 2,
    "CYP27A1-related_disorder|Cholestanol_storage_disease": 4,
    "CYP27A1-related_disorder|Cholestanol_storage_disease|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|CYP27A1-related_disorder|Cardiovascular_phenotype|not_specified|Cholestanol_storage_disease": 1,
    "not_provided|Cholestanol_storage_disease|CYP27A1-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cholestanol_storage_disease|Cardiovascular_phenotype|CYP27A1-related_disorder": 1,
    "Cholestanol_storage_disease|Senior-Loken_syndrome_1": 1,
    "CYP27A1-related_disorder": 4,
    "Cholestanol_storage_disease|not_provided|Cardiovascular_phenotype|CYP27A1-related_disorder": 1,
    "CYP27A1-related_disorder|Cardiovascular_phenotype|not_specified|Cholestanol_storage_disease": 1,
    "Cholestanol_storage_disease|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Cholestanol_storage_disease|not_provided": 1,
    "not_provided|CYP27A1-related_disorder|Cardiovascular_phenotype|Cholestanol_storage_disease": 1,
    "Cholestanol_storage_disease|CYP27A1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cholestanol_storage_disease|not_specified|not_provided": 1,
    "not_specified|Cholestanol_storage_disease|CYP27A1-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|CYP27A1-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cholestanol_storage_disease|not_provided|Cardiovascular_phenotype": 1,
    "CYP27A1-related_disorder|Intellectual_disability|Cardiovascular_phenotype|Cholestanol_storage_disease|not_provided": 1,
    "Intellectual_disability|not_provided|Cholestanol_storage_disease": 1,
    "CYP27A1-related_disorder|not_provided|Cholestanol_storage_disease|Cardiovascular_phenotype": 2,
    "Cholestanol_storage_disease|Regression_of_motor_development_with_severe_dystonia_and_corresponding_basal_ganglia_lesions|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cholestanol_storage_disease|CYP27A1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|CYP27A1-related_disorder|not_specified|not_provided|Cholestanol_storage_disease": 2,
    "CYP27A1-related_disorder|not_specified|Cholestanol_storage_disease": 1,
    "CYP27A1-related_disorder|Cholestanol_storage_disease|not_specified": 1,
    "Cardiovascular_phenotype|Cholestanol_storage_disease|not_specified": 1,
    "PRKAG3-related_disorder": 8,
    "Increased_muscle_glycogen_content": 10,
    "not_provided|PRKAG3-related_disorder": 1,
    "SKELETAL_MUSCLE_GLYCOGEN_CONTENT_AND_METABOLISM_QUANTITATIVE_TRAIT_LOCUS": 1,
    "Odonto-onycho-dermal_dysplasia|Selective_tooth_agenesis|Sch\u00f6pf-Schulz-Passarge_syndrome": 2,
    "Selective_tooth_agenesis|Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia": 10,
    "Selective_tooth_agenesis|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Selective_tooth_agenesis|not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia": 1,
    "Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 15,
    "Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4": 1,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 95,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 239,
    "Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 8,
    "Sch\u00f6pf-Schulz-Passarge_syndrome": 28,
    "not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 2,
    "Tooth_agenesis|_selective|_4": 10,
    "Odonto-onycho-dermal_dysplasia": 8,
    "Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|Inborn_genetic_diseases": 1,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 3,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome": 34,
    "WNT10A-related_disorder": 5,
    "WNT10A-related_disorder|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "WNT10A-related_disorder|Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_provided": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Sch\u00f6pf-Schulz-Passarge_syndrome|Inborn_genetic_diseases": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|WNT10A-related_disorder|not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Tooth_agenesis|_selective|_4|Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia": 3,
    "not_provided|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome": 2,
    "not_provided|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 5,
    "WNT10A-related_disorder|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Inborn_genetic_diseases|Sch\u00f6pf-Schulz-Passarge_syndrome|not_specified|not_provided|Ectodermal_dysplasia": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|WNT10A-related_disorder|not_provided": 1,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome|not_provided": 3,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome|WNT10A-related_disorder": 3,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Sch\u00f6pf-Schulz-Passarge_syndrome|not_provided": 3,
    "Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|not_provided": 2,
    "not_provided|WNT10A-related_disorder|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Selective_tooth_agenesis|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_specified|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Sch\u00f6pf-Schulz-Passarge_syndrome": 10,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Inborn_genetic_diseases|Sch\u00f6pf-Schulz-Passarge_syndrome": 2,
    "WNT10A-related_disorder|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Inborn_genetic_diseases|Bladder_exstrophy-epispadias-cloacal_extrophy_complex|not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "WNT10A-related_disorder|Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Tooth_agenesis|not_provided": 1,
    "Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|not_provided|WNT10A-related_disorder|Tooth_agenesis|_selective|_2": 1,
    "Sch\u00f6pf-Schulz-Passarge_syndrome|WNT10A-related_disorder|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 2,
    "WNT10A-related_disorder|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 1,
    "WNT10A-related_disorder|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_provided|Tooth_agenesis|_selective|_2|Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis": 1,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|not_specified|not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "not_provided|not_specified|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 1,
    "not_provided|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Inborn_genetic_diseases|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "not_specified|WNT10A-related_disorder|not_provided|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 1,
    "Inborn_genetic_diseases|Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_provided|Palmoplantar_keratoderma|Stiff_skin|Arthralgia|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Tooth_agenesis|_selective|_4|Sch\u00f6pf-Schulz-Passarge_syndrome|Hypohidrotic_ectodermal_dysplasia|Ectodermal_dysplasia_WNT10A_related|WNT10A-related_disorder|Inborn_genetic_diseases|Odonto-onycho-dermal_dysplasia|not_provided|Ectodermal_dysplasia|Tooth_agenesis|See_cases": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|WNT10A-related_disorder|Sch\u00f6pf-Schulz-Passarge_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_provided|Inborn_genetic_diseases": 1,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|WNT10A-related_disorder|Sch\u00f6pf-Schulz-Passarge_syndrome": 2,
    "Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "not_provided|Sch\u00f6pf-Schulz-Passarge_syndrome": 2,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|Inborn_genetic_diseases|Sch\u00f6pf-Schulz-Passarge_syndrome": 2,
    "Abnormality_of_the_dentition": 2,
    "not_provided|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 2,
    "Inborn_genetic_diseases|Sch\u00f6pf-Schulz-Passarge_syndrome": 1,
    "Tooth_agenesis|_selective|_4|Odonto-onycho-dermal_dysplasia|not_provided": 2,
    "Sch\u00f6pf-Schulz-Passarge_syndrome|Odonto-onycho-dermal_dysplasia|not_provided|Tooth_agenesis|_selective|_4": 2,
    "not_specified|Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|not_provided": 1,
    "Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|not_specified|not_provided|Tooth_agenesis": 1,
    "Odonto-onycho-dermal_dysplasia|Tooth_agenesis|_selective|_4|Inborn_genetic_diseases": 1,
    "Odonto-onycho-dermal_dysplasia|Sch\u00f6pf-Schulz-Passarge_syndrome|Tooth_agenesis|_selective|_4|not_provided": 1,
    "Early-onset_anterior_polar_cataract|not_specified": 1,
    "not_specified|CRYBA2-related_disorder": 2,
    "CRYBA2-related_disorder": 3,
    "Cataract_42": 2,
    "CRYBA2-related_disorder|not_specified": 1,
    "Early-onset_anterior_polar_cataract": 1,
    "Spermatogenic_failure_40": 8,
    "not_provided|Non-syndromic_male_infertility_due_to_sperm_motility_disorder": 1,
    "CFAP65-related_disorder": 2,
    "not_provided|CFAP65-related_disorder": 1,
    "Brachydactyly_type_A1": 43,
    "Brachydactyly": 83,
    "Brachydactyly_type_A1|not_provided": 8,
    "not_provided|Brachydactyly_type_A1": 14,
    "Brachydactyly_type_A1|not_provided|not_specified": 1,
    "not_specified|not_provided|Acrocapitofemoral_dysplasia": 1,
    "Brachydactyly_type_A1|Acrocapitofemoral_dysplasia": 2,
    "not_provided|IHH-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|IHH-related_disorder": 1,
    "Acrocapitofemoral_dysplasia": 7,
    "Acromesomelic_dysplasia_1|_Maroteaux_type": 53,
    "IHH-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "IHH-Related_Disorders|not_provided": 1,
    "not_specified|not_provided|IHH-related_disorder": 1,
    "IHH-related_disorder": 3,
    "Inborn_genetic_diseases|Brachydactyly_type_A1": 1,
    "not_provided|not_specified|Brachydactyly_type_A1": 2,
    "IHH-related_disorder|not_provided|not_specified|Brachydactyly_type_A1": 1,
    "Brachydactyly_type_A1|IHH-related_disorder|not_provided": 1,
    "Acrocapitofemoral_dysplasia|Brachydactyly_type_A1A": 2,
    "Brachydactyly_type_A1|not_provided|Brachydactyly_type_A1A|Acrocapitofemoral_dysplasia": 1,
    "Brachydactyly_type_A1A": 2,
    "not_provided|not_specified|Acrocapitofemoral_dysplasia|Brachydactyly_type_A1": 1,
    "Inborn_genetic_diseases|Brachydactyly_type_A1|not_provided": 1,
    "IHH-related_disorder|not_specified|not_provided|Brachydactyly_type_A1": 2,
    "not_provided|Acrocapitofemoral_dysplasia|Brachydactyly_type_A1": 1,
    "not_provided|Acrocapitofemoral_dysplasia": 1,
    "Brachydactyly_type_A1A|not_provided|Brachydactyly_type_A1": 1,
    "Brachydactyly_type_A1|not_specified|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Brachydactyly_type_A1": 1,
    "Inborn_genetic_diseases|IHH-related_disorder|not_provided": 1,
    "not_provided|Brachydactyly": 5,
    "Cernunnos-XLF_deficiency": 144,
    "Cernunnos-XLF_deficiency|not_specified|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Cernunnos-XLF_deficiency": 6,
    "Cernunnos-XLF_deficiency|Inborn_genetic_diseases": 7,
    "not_provided|Cernunnos-XLF_deficiency|NHEJ1-related_disorder|not_specified": 1,
    "Cernunnos-XLF_deficiency|not_provided|not_specified": 2,
    "not_specified|not_provided|Cernunnos-XLF_deficiency": 2,
    "Cernunnos-XLF_deficiency|not_specified|not_provided": 2,
    "Isolated_anophthalmia-microphthalmia_syndrome|Microphthalmia/coloboma_13": 1,
    "not_provided|Cernunnos-XLF_deficiency": 6,
    "Cernunnos-XLF_deficiency|not_provided": 3,
    "NHEJ1-related_disorder|not_specified|not_provided|Cernunnos-XLF_deficiency": 2,
    "Severe_combined_immunodeficiency_disease|Cernunnos-XLF_deficiency": 1,
    "Microphthalmia|_isolated|_with_coloboma_7": 6,
    "ABCB6-related_disorder|not_provided": 3,
    "not_provided|ABCB6-related_disorder": 2,
    "Microphthalmia|_isolated|_with_coloboma_7|Langereis_blood_group|Familial_pseudohyperkalemia|Dyschromatosis_universalis_hereditaria_3": 2,
    "ABCB6-related_disorder": 6,
    "Langereis_blood_group": 5,
    "not_provided|Microphthalmia|_isolated|_with_coloboma_7|ABCB6-related_disorder": 1,
    "not_specified|not_provided|Familial_pseudohyperkalemia|ABCB6-related_disorder": 1,
    "Dyschromatosis_universalis_hereditaria_3": 7,
    "Langereis_blood_group|not_provided": 1,
    "Hereditary_coproporphyria|Protoporphyria|_erythropoietic|_1|Acute_intermittent_porphyria|not_provided|Variegate_porphyria": 1,
    "not_provided|Dyschromatosis_universalis_hereditaria_3": 1,
    "Hereditary_coproporphyria|Variegate_porphyria|Acute_intermittent_porphyria|not_provided|Protoporphyria|_erythropoietic|_1|not_specified": 1,
    "Familial_pseudohyperkalemia|Microphthalmia|_isolated|_with_coloboma_7|Dyschromatosis_universalis_hereditaria_3|not_provided": 1,
    "Protoporphyria|_erythropoietic|_1|not_provided|ABCB6-related_disorder|Variegate_porphyria|Hereditary_coproporphyria|Acute_intermittent_porphyria": 1,
    "Dyschromatosis_universalis_hereditaria_3|Familial_pseudohyperkalemia|Microphthalmia|_isolated|_with_coloboma_7|Langereis_blood_group|ABCB6-related_disorder|not_provided": 1,
    "Familial_pseudohyperkalemia": 1,
    "Langereis_blood_group|Microphthalmia|_isolated|_with_coloboma_7|Familial_pseudohyperkalemia|Dyschromatosis_universalis_hereditaria_3": 1,
    "not_provided|Protoporphyria|_erythropoietic|_1|ABCB6-related_disorder|Acute_intermittent_porphyria": 1,
    "not_provided|Hereditary_coproporphyria|Variegate_porphyria|Protoporphyria|_erythropoietic|_1|Acute_intermittent_porphyria": 1,
    "Acute_intermittent_porphyria|Protoporphyria|_erythropoietic|_1|not_provided": 1,
    "not_provided|Langereis_blood_group": 1,
    "not_provided|Familial_pseudohyperkalemia|Langereis_blood_group|Microphthalmia|_isolated|_with_coloboma_7|Dyschromatosis_universalis_hereditaria_3|ABCB6-related_disorder": 1,
    "Dyschromatosis_universalis_hereditaria_3|not_provided": 1,
    "ABCB6-related_disorder|not_provided|Microphthalmia|_isolated|_with_coloboma_7|Variegate_porphyria|Protoporphyria|_erythropoietic|_1|Acute_intermittent_porphyria": 1,
    "ABCB6-related_disorder|not_provided|Langereis_blood_group|Hereditary_coproporphyria|Variegate_porphyria|Acute_intermittent_porphyria|Protoporphyria|_erythropoietic|_1": 1,
    "not_provided|not_specified|Microphthalmia|_isolated|_with_coloboma_7": 1,
    "ANKZF1-related_disorder|not_provided": 11,
    "not_provided|ANKZF1-related_disorder": 19,
    "ANKZF1-related_disorder": 4,
    "not_specified|ANKZF1-related_disorder": 1,
    "ANKZF1-related_disorder|not_specified|not_provided": 1,
    "TUBA4A-related_disorder": 34,
    "not_provided|TUBA4A-related_disorder": 4,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_22": 1,
    "Amyotrophic_lateral_sclerosis_type_22": 11,
    "OOCYTE/ZYGOTE/EMBRYO_MATURATION_ARREST_23": 6,
    "TUBA4A-related_disorder|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_22|not_provided": 2,
    "not_provided|TUBA4A-related_disorder|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_22|TUBA4A-related_disorder": 1,
    "TUBA4A-related_disorder|not_specified": 1,
    "SPASTIC_ATAXIA_11|_AUTOSOMAL_DOMINANT": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_22": 1,
    "Ptosis": 3,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 189,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_provided": 10,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Autosomal_recessive_distal_spinal_muscular_atrophy_2|Charcot-Marie-Tooth_disease": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 6,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease": 5,
    "DNAJB2-related_disorder": 3,
    "DNAJB2-related_disorder|Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 9,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease|not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 1,
    "DNAJB2-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2T": 23,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_2|DNAJB2-related_disorder|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Inborn_genetic_diseases": 4,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_specified": 3,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Inborn_genetic_diseases": 2,
    "DNAJB2-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_specified|DNAJB2-related_disorder|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_5|not_provided|not_specified": 1,
    "Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 2,
    "Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 6,
    "not_specified|Myofibrillar_Myopathy|_Dominant|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "not_provided|Dilated_cardiomyopathy_1I|not_specified": 1,
    "Desmin-related_myofibrillar_myopathy|not_specified|Myofibrillar_Myopathy|_Dominant|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Cardiovascular_phenotype": 3,
    "Desmin-related_myofibrillar_myopathy|Primary_familial_dilated_cardiomyopathy|not_provided": 1,
    "DES-related_disorder": 4,
    "Desmin-related_myofibrillar_myopathy|not_provided": 62,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided": 4,
    "not_specified|Myofibrillar_Myopathy|_Dominant|Cardiomyopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided": 1,
    "not_specified|Desmin-related_myofibrillar_myopathy": 11,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype": 57,
    "Primary_dilated_cardiomyopathy|Neuromuscular_disease|Desmin-related_myofibrillar_myopathy|not_provided": 1,
    "not_provided|Desmin-related_myofibrillar_myopathy": 32,
    "Primary_dilated_cardiomyopathy|Desmin-related_myofibrillar_myopathy|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided": 11,
    "Myofibrillar_myopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy": 10,
    "Cardiovascular_phenotype|not_provided|Desmin-related_myofibrillar_myopathy": 10,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 2,
    "not_provided|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|DES-related_disorder": 1,
    "Cardiovascular_phenotype|Myofibrillar_Myopathy|_Dominant|Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 2,
    "Desmin-related_myofibrillar_myopathy|not_provided|not_specified": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Desmin-related_myofibrillar_myopathy": 2,
    "Dilated_cardiomyopathy_1I|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|DES-related_disorder|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_specified|not_provided": 3,
    "DES-related_disorder|not_provided|Cardiovascular_phenotype|not_specified|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|not_specified": 3,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|not_provided": 7,
    "Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|not_specified|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 7,
    "Desmin-related_myofibrillar_myopathy|not_specified|not_provided": 4,
    "Desmin-related_myofibrillar_myopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|not_specified|Cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|DES-related_disorder|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified": 7,
    "not_specified|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy": 3,
    "Primary_dilated_cardiomyopathy|Desmin-related_myofibrillar_myopathy|not_provided|Cardiovascular_phenotype": 1,
    "Desmin-related_myofibrillar_myopathy|not_specified|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided": 1,
    "Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|Desmin-related_myofibrillar_myopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Desmin-related_myofibrillar_myopathy": 1,
    "Dilated_cardiomyopathy_1I|not_provided|Myofibrillar_Myopathy|_Dominant|not_specified|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Dilated_cardiomyopathy_1I": 2,
    "Desmin-related_myofibrillar_myopathy|not_specified": 8,
    "Desmin-related_myofibrillar_myopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|not_provided": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Cardiovascular_phenotype|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "DES-related_disorder|Desmin-related_myofibrillar_myopathy": 2,
    "Desmin-related_myofibrillar_myopathy|DES-related_disorder": 1,
    "Desmin-related_myofibrillar_myopathy|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided": 1,
    "Dilated_cardiomyopathy_1S|not_provided|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_Myopathy|_Dominant|not_provided|not_specified|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|DES-related_disorder": 1,
    "not_provided|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Cardiovascular_phenotype": 1,
    "not_specified|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype": 3,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I": 2,
    "not_provided|Desmin-related_myofibrillar_myopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Limb-girdle_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_specified|DES-related_disorder|Desmin-related_myofibrillar_myopathy": 1,
    "Dilated_cardiomyopathy_1I|Myofibrillar_Myopathy|_Dominant|not_specified|Desmin-related_myofibrillar_myopathy|not_provided|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy": 1,
    "Primary_dilated_cardiomyopathy|Neuromuscular_disease|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 2,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Left_ventricular_noncompaction_cardiomyopathy|See_cases": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Myofibrillar_Myopathy|_Dominant|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Myofibrillar_myopathy|not_specified|not_provided|Cardiomyopathy|Congenital_diaphragmatic_hernia": 1,
    "not_specified|not_provided|Desmin-related_myofibrillar_myopathy": 1,
    "not_specified|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Cardiovascular_phenotype|DES-related_disorder|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype": 6,
    "Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|Dilated_cardiomyopathy_1I|Cardiovascular_phenotype|not_specified|not_provided|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Myofibrillar_Myopathy|_Dominant|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "not_specified|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Dilated_cardiomyopathy_1I": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 3,
    "not_provided|Desmin-related_myofibrillar_myopathy|Myofibrillar_myopathy|not_specified": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "DES-related_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy": 2,
    "DES-related_disorder|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Myofibrillar_Myopathy|_Dominant|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|Cardiomyopathy|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiomyopathy|not_specified|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype": 1,
    "Desmin-related_myofibrillar_myopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1I|Myofibrillar_Myopathy|_Dominant|not_provided|not_specified|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "not_provided|Desmin-related_myofibrillar_myopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Desmin-related_myofibrillar_myopathy|not_specified": 1,
    "Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|DES-related_disorder|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|not_specified|Cardiomyopathy|Scapuloperoneal_weakness": 1,
    "Cardiovascular_phenotype|not_specified|Desmin-related_myofibrillar_myopathy": 2,
    "Desmin-related_myofibrillar_myopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_specified|not_provided|DES-related_disorder|Myofibrillar_Myopathy|_Dominant": 1,
    "not_specified|Desmin-related_myofibrillar_myopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "DES-related_disorder|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Dilated_cardiomyopathy_1I": 2,
    "Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I": 1,
    "Cardiomyopathy|DES-related_disorder": 1,
    "Desmin-related_myofibrillar_myopathy|not_specified|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided": 1,
    "not_specified|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided": 1,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|not_provided": 1,
    "Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_specified|Myofibrillar_Myopathy|_Dominant|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|not_provided": 1,
    "Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Myofibrillar_Myopathy|_Dominant|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|Cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|not_provided": 1,
    "DES-related_disorder|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1I|Primary_dilated_cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Cardiovascular_phenotype|not_provided|DES-related_disorder": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided": 2,
    "not_provided|Myofibrillar_myopathy": 1,
    "not_provided|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Myofibrillar_Myopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided|Dilated_cardiomyopathy_1A": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|Cardiomyopathy": 1,
    "Bradycardia|Progressive_familial_heart_block": 1,
    "DES-related_disorder|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_provided|DES-related_disorder|Cardiovascular_phenotype": 1,
    "Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy": 2,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Cardiovascular_phenotype|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_specified|not_provided": 1,
    "Cardiomyopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|DES-related_disorder|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|not_provided|Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type": 1,
    "Desmin-related_myofibrillar_myopathy|Dilated_cardiomyopathy_1I": 3,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1I|Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|Neuromuscular_disease|Primary_dilated_cardiomyopathy|Primary_familial_dilated_cardiomyopathy|not_provided": 1,
    "Desmin-related_myofibrillar_myopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|not_specified": 1,
    "Dilated_cardiomyopathy_1I|Cardiovascular_phenotype|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Desmin-related_myofibrillar_myopathy|not_provided": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|Abnormality_of_the_musculature": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 24,
    "Desmin-related_myofibrillar_myopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Cardiovascular_phenotype": 1,
    "Desmin-related_myofibrillar_myopathy|Myofibrillar_myopathy|not_provided": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Neuromuscular_disease|Primary_dilated_cardiomyopathy|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|DES-related_disorder|Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1I|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Primary_dilated_cardiomyopathy": 1,
    "Desmin-related_myofibrillar_myopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 3,
    "Desmin-related_myofibrillar_myopathy|not_provided|Myofibrillar_Myopathy|_Dominant|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Desmin-related_myofibrillar_myopathy|Scapuloperoneal_weakness": 1,
    "Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|not_provided|Neurogenic_scapuloperoneal_syndrome|_Kaeser_type|Dilated_cardiomyopathy_1I": 1,
    "not_provided|Scapuloperoneal_weakness|Desmin-related_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myopathy|_centronuclear|_5": 58,
    "Inborn_genetic_diseases|not_provided|Myopathy|_centronuclear|_5|not_specified": 1,
    "not_provided|Myopathy|_centronuclear|_5": 26,
    "Inborn_genetic_diseases|Myopathy|_centronuclear|_5|not_provided": 6,
    "Myopathy|_centronuclear|_5|Inborn_genetic_diseases": 7,
    "SPEG-related_disorder|not_provided": 29,
    "not_provided|Myopathy|_centronuclear|_5|Inborn_genetic_diseases": 11,
    "SPEG-related_disorder": 11,
    "Myopathy|_centronuclear|_5|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|SPEG-related_disorder": 2,
    "SPEG-related_congenital_myopathy": 1,
    "Myopathy|_centronuclear|_5|not_specified|not_provided": 1,
    "Myopathy|_centronuclear|_5|not_provided": 16,
    "not_provided|SPEG-related_disorder": 28,
    "Inborn_genetic_diseases|not_provided|Myopathy|_centronuclear|_5": 2,
    "Inborn_genetic_diseases|Myopathy|_centronuclear|_5": 5,
    "Myopathy|_centronuclear|_5|Inborn_genetic_diseases|SPEG-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Myopathy|_centronuclear|_5": 3,
    "not_provided|SPEG-related_disorder|Myopathy|_centronuclear|_5|not_specified": 1,
    "Inborn_genetic_diseases|SPEG-related_disorder|not_provided": 2,
    "not_specified|Congenital_myopathy": 1,
    "SPEG-related_congenital_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SPEG-related_disorder|Myopathy|_centronuclear|_5": 1,
    "not_specified|SPEG-related_disorder|not_provided": 1,
    "Myopathy|_centronuclear|_5|not_provided|Inborn_genetic_diseases": 2,
    "SPEG-related_disorder|not_specified|not_provided": 2,
    "SPEG-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Myopathy|_centronuclear|_5": 1,
    "Autosomal_dominant_centronuclear_myopathy|Myopathy|_centronuclear|_5|SPEG-related_disorder|not_provided": 1,
    "SPEG-related_disorder|Myopathy|_centronuclear|_5|Inborn_genetic_diseases|not_provided": 1,
    "Myopathy|_centronuclear|_5|SPEG-related_disorder|not_provided": 1,
    "Myopathy|_centronuclear|_5|not_provided|not_specified|SPEG-related_disorder": 1,
    "Inborn_genetic_diseases|Myopathy|_centronuclear|_5|not_provided|SPEG-related_disorder": 1,
    "Myopathy|_centronuclear|_5|Inborn_genetic_diseases|SPEG-related_disorder|not_provided": 1,
    "not_specified|not_provided|Myopathy|_centronuclear|_5": 1,
    "Myopathy|_centronuclear|_5|Myopathy|_centronuclear|_2": 1,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome": 56,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_specified": 3,
    "not_specified|not_provided|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 3,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_provided": 2,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 5,
    "GMPPA-related_disorder|Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_provided|not_specified": 1,
    "not_provided|Chromosomal_instability_with_tissue-specific_radiosensitivity|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 1,
    "not_specified|Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_provided": 2,
    "not_provided|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 5,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_specified|not_provided": 3,
    "not_specified|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 2,
    "not_specified|Inborn_genetic_diseases|Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_provided|GMPPA-related_disorder": 1,
    "GMPPA-related_disorder|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 1,
    "GMPPA-related_disorder": 1,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_provided|GMPPA-related_disorder": 2,
    "GMPPA-related_disorder|Alacrima|_achalasia|_and_intellectual_disability_syndrome|not_provided": 1,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Alacrima|_achalasia|_and_intellectual_disability_syndrome": 1,
    "Alacrima|_achalasia|_and_intellectual_disability_syndrome|Inborn_genetic_diseases|GMPPA-related_disorder": 1,
    "3-M_syndrome": 10,
    "3M_syndrome_2|not_provided": 55,
    "3M_syndrome_2": 95,
    "not_provided|3M_syndrome_2": 32,
    "3M_syndrome_2|not_provided|not_specified": 6,
    "not_specified|3M_syndrome_2|not_provided": 3,
    "3M_syndrome_2|Inborn_genetic_diseases|not_provided": 3,
    "3M_syndrome_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|3M_syndrome_2|not_specified": 10,
    "not_specified|not_provided|3M_syndrome_2": 7,
    "OBSL1-related_disorder|not_provided": 8,
    "3M_syndrome_2|not_provided|Inborn_genetic_diseases": 6,
    "3M_syndrome_2|not_specified|not_provided": 10,
    "not_specified|3M_syndrome_2": 1,
    "Inborn_genetic_diseases|3M_syndrome_2|not_provided": 8,
    "OBSL1-related_disorder|3M_syndrome_2|not_specified|not_provided": 1,
    "OBSL1-related_disorder|not_provided|3M_syndrome_2": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|3M_syndrome_2": 1,
    "OBSL1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|OBSL1-related_disorder|3M_syndrome_2|not_provided": 2,
    "OBSL1-related_disorder": 12,
    "3M_syndrome_2|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "OBSL1-related_disorder|3M_syndrome_2|not_provided": 3,
    "OBSL1-related_disorder|not_specified|not_provided|3M_syndrome_2": 4,
    "not_provided|3M_syndrome_2|Inborn_genetic_diseases": 8,
    "not_specified|OBSL1-related_disorder|not_provided": 1,
    "3M_syndrome_2|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|not_specified|3M_syndrome_2": 1,
    "not_provided|Inborn_genetic_diseases|3M_syndrome_2": 1,
    "Inborn_genetic_diseases|3M_syndrome_2|OBSL1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|3M_syndrome_2": 2,
    "3M_syndrome_2|OBSL1-related_disorder|not_provided": 1,
    "not_specified|not_provided|OBSL1-related_disorder": 1,
    "not_provided|OBSL1-related_disorder": 6,
    "not_specified|not_provided|3M_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|OBSL1-related_disorder|not_specified|3M_syndrome_2": 1,
    "Inborn_genetic_diseases|not_provided|3M_syndrome_2": 2,
    "Inborn_genetic_diseases|3M_syndrome_2|OBSL1-related_disorder": 1,
    "not_provided|3M_syndrome_2|OBSL1-related_disorder": 1,
    "3M_syndrome_1": 102,
    "3M_syndrome_2|not_provided|OBSL1-related_disorder": 3,
    "3M_syndrome_1|not_specified": 1,
    "3M_syndrome_1|3M_syndrome_2": 1,
    "3M_syndrome_2|Short_stature": 1,
    "Inborn_genetic_diseases|3M_syndrome_2|not_provided|OBSL1-related_disorder": 1,
    "3M_syndrome_2|OBSL1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|3M_syndrome_2": 1,
    "3M_syndrome_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "3-M_syndrome|not_provided": 5,
    "INHA-related_disorder": 3,
    "not_specified|not_provided|INHA-related_disorder|Premature_ovarian_failure": 1,
    "SLC4A3-related_disorder": 7,
    "not_provided|SLC4A3-related_disorder": 1,
    "Short_QT_syndrome_7": 4,
    "SLC4A3-related_disorder|not_specified|not_provided": 1,
    "SLC4A3-related_disorder|Inborn_genetic_diseases": 1,
    "Short_QT_syndrome_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SLC4A3-related_disorder": 1,
    "SLC4A3-related_disorder|not_specified": 1,
    "not_specified|not_provided|EPHA4-related_disorder": 1,
    "not_provided|EPHA4-related_disorder": 1,
    "PAX3-related_disorder": 12,
    "Waardenburg_syndrome_type_1": 94,
    "Waardenburg_syndrome|Craniofacial-deafness-hand_syndrome": 10,
    "Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome": 7,
    "Waardenburg_syndrome|Craniofacial-deafness-hand_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|PAX3-related_disorder": 1,
    "Waardenburg_syndrome|Craniofacial-deafness-hand_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome": 2,
    "Waardenburg_syndrome": 9,
    "not_provided|PAX3-related_disorder": 3,
    "Waardenburg_syndrome_type_1|not_provided": 7,
    "not_provided|not_specified|Waardenburg_syndrome|Craniofacial-deafness-hand_syndrome": 1,
    "Inborn_genetic_diseases|Hearing_impairment": 7,
    "Waardenburg_syndrome|Hearing_impairment|not_specified|not_provided|Craniofacial-deafness-hand_syndrome": 1,
    "PAX3-related_disorder|not_provided": 4,
    "not_provided|Alveolar_rhabdomyosarcoma|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome_type_1|Waardenburg_syndrome_type_3": 1,
    "Inborn_genetic_diseases|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome": 1,
    "Waardenburg_syndrome|Usher_syndrome|not_specified|not_provided|Craniofacial-deafness-hand_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome_type_1|Alveolar_rhabdomyosarcoma|Waardenburg_syndrome_type_3": 1,
    "not_provided|not_specified|PAX3-related_disorder": 1,
    "not_provided|not_specified|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome": 1,
    "not_specified|Waardenburg_syndrome_type_1|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome|not_provided|Congenital_diaphragmatic_hernia": 1,
    "Rare_genetic_deafness|Waardenburg_syndrome|not_provided|Waardenburg_syndrome_type_1": 1,
    "Waardenburg_syndrome|not_specified|not_provided|Craniofacial-deafness-hand_syndrome": 2,
    "Waardenburg_syndrome_type_1|See_cases|Rare_genetic_deafness|not_provided": 1,
    "Waardenburg_syndrome|PAX3-related_disorder|not_provided|not_specified|Craniofacial-deafness-hand_syndrome": 1,
    "Waardenburg_syndrome_type_3": 6,
    "Waardenburg_syndrome_type_1|Alveolar_rhabdomyosarcoma|Waardenburg_syndrome_type_3|Craniofacial-deafness-hand_syndrome|not_provided": 1,
    "not_provided|Waardenburg_syndrome|Waardenburg_syndrome_type_1": 1,
    "not_specified|PAX3-related_disorder|Waardenburg_syndrome|Craniofacial-deafness-hand_syndrome|not_provided": 1,
    "PAX3-related_disorder|Waardenburg_syndrome_type_1": 2,
    "not_provided|Waardenburg_syndrome_type_1": 10,
    "Craniofacial-deafness-hand_syndrome": 1,
    "Ocular_albinism_with_congenital_sensorineural_hearing_loss": 1,
    "Craniofacial-deafness-hand_syndrome|Alveolar_rhabdomyosarcoma|Waardenburg_syndrome_type_1|Waardenburg_syndrome_type_3": 1,
    "Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome_type_1|Waardenburg_syndrome_type_3|not_provided": 1,
    "Waardenburg_syndrome|Rare_genetic_deafness|not_provided|Waardenburg_syndrome_type_1": 1,
    "not_provided|Waardenburg_syndrome_type_1|Waardenburg_syndrome_type_3": 1,
    "not_specified|not_provided|PAX3-related_disorder": 1,
    "PAX3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Craniofacial-deafness-hand_syndrome|Alveolar_rhabdomyosarcoma|Waardenburg_syndrome_type_1|Waardenburg_syndrome_type_3|Waardenburg_syndrome|not_specified": 1,
    "not_specified|PAX3-related_disorder|not_provided": 1,
    "Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome|not_provided": 1,
    "not_specified|Alveolar_rhabdomyosarcoma|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome_type_3|Waardenburg_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "PAX3-related_disorder|Inborn_genetic_diseases|Waardenburg_syndrome|not_specified|not_provided|Waardenburg_syndrome_type_1|Craniofacial-deafness-hand_syndrome": 1,
    "Waardenburg_syndrome_type_3|Craniofacial-deafness-hand_syndrome": 1,
    "Waardenburg_syndrome_type_1|Craniofacial-deafness-hand_syndrome|Alveolar_rhabdomyosarcoma|Waardenburg_syndrome_type_3": 1,
    "Waardenburg_syndrome|Waardenburg_syndrome_type_1": 2,
    "not_provided|Waardenburg_syndrome|not_specified|Craniofacial-deafness-hand_syndrome": 1,
    "Intellectual_disability|Waardenburg_syndrome_type_1|not_provided": 1,
    "Waardenburg_syndrome_type_1|not_provided|Waardenburg_syndrome_type_3": 1,
    "Rare_genetic_deafness|Waardenburg_syndrome_type_3|not_provided": 1,
    "Waardenburg_syndrome_type_1|not_provided|PAX3-related_disorder": 1,
    "Waardenburg_syndrome_type_3|Alveolar_rhabdomyosarcoma|Waardenburg_syndrome_type_1|Craniofacial-deafness-hand_syndrome": 1,
    "Waardenburg_syndrome|not_provided|Waardenburg_syndrome_type_1": 1,
    "Waardenburg_syndrome_type_3|Waardenburg_syndrome_type_1": 1,
    "not_provided|Craniofacial-deafness-hand_syndrome": 1,
    "Waardenburg_syndrome_type_1|Waardenburg_syndrome_type_3|Craniofacial-deafness-hand_syndrome|Waardenburg_syndrome|not_specified|not_provided": 1,
    "Waardenburg_syndrome|not_specified|PAX3-related_disorder|Craniofacial-deafness-hand_syndrome|not_provided": 1,
    "Waardenburg_syndrome_type_1|Intellectual_disability|not_provided": 1,
    "Waardenburg_syndrome_type_3|Waardenburg_syndrome_type_1|Craniofacial-deafness-hand_syndrome": 1,
    "FARSB-related_disorder": 3,
    "FARSB-related_disorder|not_provided": 3,
    "not_provided|FARSB-related_disorder": 7,
    "not_provided|Rajab_interstitial_lung_disease_with_brain_calcifications_1": 1,
    "not_provided|Rajab_interstitial_lung_disease_with_brain_calcifications|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 1,
    "Rajab_interstitial_lung_disease_with_brain_calcifications_1": 3,
    "Rajab_interstitial_lung_disease_with_brain_calcifications|Cirrhosis_of_liver|Cerebral_calcification|Interstitial_pneumonitis|Vascular_dilatation": 3,
    "Rajab_interstitial_lung_disease_with_brain_calcifications|not_provided": 1,
    "Rajab_interstitial_lung_disease_with_brain_calcifications_1|not_provided|Rajab_interstitial_lung_disease_with_brain_calcifications": 1,
    "Rajab_interstitial_lung_disease_with_brain_calcifications|Rajab_interstitial_lung_disease_with_brain_calcifications_1|not_provided": 1,
    "Cirrhosis_of_liver|Cerebral_calcification|Interstitial_pneumonitis|Vascular_dilatation": 2,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Rajab_interstitial_lung_disease_with_brain_calcifications_1|Rajab_interstitial_lung_disease_with_brain_calcifications": 1,
    "not_provided|FARSB-related_disorder|Inborn_genetic_diseases": 1,
    "FARSB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "AP1S3-related_disorder": 5,
    "Psoriasis_15|_pustular|_susceptibility_to|not_provided": 1,
    "AP1S3-related_disorder|Psoriasis_15|_pustular|_susceptibility_to|not_specified|not_provided": 1,
    "not_provided|AP1S3-related_disorder|Psoriasis_15|_pustular|_susceptibility_to": 1,
    "AP1S3-related_disorder|Psoriasis_15|_pustular|_susceptibility_to|not_provided": 1,
    "not_provided|AP1S3-related_disorder": 1,
    "not_provided|MRPL44-related_disorder": 1,
    "MRPL44-related_disorder|not_specified": 1,
    "Infantile_hypertrophic_cardiomyopathy_due_to_MRPL44_deficiency": 2,
    "Infantile_hypertrophic_cardiomyopathy_due_to_MRPL44_deficiency|not_provided": 2,
    "not_provided|Infantile_hypertrophic_cardiomyopathy_due_to_MRPL44_deficiency": 1,
    "MRPL44-related_disorder|not_specified|not_provided": 1,
    "MRPL44-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Infantile_hypertrophic_cardiomyopathy_due_to_MRPL44_deficiency|not_provided": 1,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 145,
    "not_provided|not_specified|Infantile_hypertrophic_cardiomyopathy_due_to_MRPL44_deficiency": 1,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohypoaldosteronism_type_2E": 26,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided|Pseudohypoaldosteronism_type_2E": 4,
    "Pseudohypoaldosteronism_type_2E": 42,
    "Pseudohypoaldosteronism_type_2E|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 2,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1": 133,
    "Pseudohypoaldosteronism_type_2E|Autosomal_dominant_pseudohypoaldosteronism_type_1": 8,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohypoaldosteronism_type_2E|not_provided": 6,
    "Pseudohypoaldosteronism_type_2E|not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1": 2,
    "not_provided|Pseudohypoaldosteronism_type_2E|Autosomal_dominant_pseudohypoaldosteronism_type_1": 2,
    "not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1": 17,
    "Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures": 32,
    "Neurodevelopmental_disorder_with_or_without_autism_or_seizures": 19,
    "not_provided|CUL3-related_disorder": 2,
    "Neurodevelopmental_disorder_with_or_without_autism_or_seizures|not_provided": 5,
    "not_provided|Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures": 5,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|CUL3-related_disorder|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 1,
    "Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 3,
    "not_provided|Pseudohypoaldosteronism_type_2E|not_specified|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "not_provided|Pseudohypoaldosteronism_type_2E": 6,
    "Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Inborn_genetic_diseases": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_AUTISM_AND_SEIZURES": 1,
    "CUL3-related_disorder": 11,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 19,
    "not_provided|Pseudohypoaldosteronism_type_2E|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_delay": 1,
    "Pseudohypoaldosteronism_type_2E|not_provided": 3,
    "Autism_spectrum_disorder|not_provided|Neurodevelopmental_disorder_with_or_without_autism_or_seizures": 1,
    "Abnormal_cardiovascular_system_morphology|not_provided": 2,
    "Pseudohypoaldosteronism_type_2E|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided|not_specified": 1,
    "not_provided|Pseudohypoaldosteronism_type_2E|CUL3-related_disorder": 1,
    "Pseudohypoaldosteronism_type_2A": 19,
    "CUL3-related_disorder|not_provided": 2,
    "Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Pseudohypoaldosteronism_type_2E": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITHOUT_AUTISM_OR_SEIZURES": 1,
    "Pseudohypoaldosteronism_type_2E|Pseudohypoaldosteronism_type_2A": 4,
    "Pseudohypoaldosteronism_type_2A|Pseudohypoaldosteronism_type_2E": 2,
    "Pseudohypoaldosteronism_type_2A|Pseudohypoaldosteronism_type_2E|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Pseudohypoaldosteronism_type_2E|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_without_autism_with_seizures": 2,
    "Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|not_provided": 2,
    "CUL3-related_disorder|Pseudohypoaldosteronism_type_2E|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_AUTISM_WITHOUT_SEIZURES": 1,
    "Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Pseudohypoaldosteronism_type_2E|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CUL3-related_disorder": 1,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohypoaldosteronism_type_2E|Neurodevelopmental_disorder_with_or_without_autism_or_seizures|not_provided": 1,
    "not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1|NEURODEVELOPMENTAL_DISORDER_WITHOUT_AUTISM_OR_SEIZURES": 1,
    "Neurodevelopmental_disorder_with_or_without_autism_or_seizures|Pseudohypoaldosteronism_type_2E|not_specified|not_provided": 1,
    "IRS1-related_disorder": 4,
    "not_provided|IRS1-related_disorder": 2,
    "not_provided|Type_2_diabetes_mellitus": 15,
    "Insulin_resistance|_susceptibility_to": 2,
    "not_specified|not_provided|Type_2_diabetes_mellitus": 2,
    "IRS1-related_disorder|not_specified": 1,
    "Type_2_diabetes_mellitus|IRS1-related_disorder|not_provided": 1,
    "not_specified|Type_2_diabetes_mellitus|IRS1-related_disorder|not_provided": 1,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 106,
    "Alport_syndrome|not_provided": 109,
    "Alport_syndrome": 418,
    "not_provided|Alport_syndrome": 104,
    "Kidney_disorder|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome": 8,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 195,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|COL4A4-related_disorder": 16,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|X-linked_Alport_syndrome": 1,
    "Kidney_disorder|Alport_syndrome|not_provided|not_specified": 2,
    "Autosomal_dominant_Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 2,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified|not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 5,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 32,
    "Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided": 2,
    "Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_provided|Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "not_provided|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 5,
    "Autosomal_recessive_Alport_syndrome": 333,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 30,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 53,
    "Alport_syndrome|not_specified|not_provided|Autosomal_recessive_Alport_syndrome": 3,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome": 7,
    "Autosomal_recessive_Alport_syndrome|not_provided": 32,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome": 2,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Alport_syndrome|not_provided": 1,
    "Alport_syndrome|COL4A4-related_disorder|not_provided": 4,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 17,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Alport_syndrome|not_provided": 14,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided": 6,
    "Benign_familial_hematuria": 24,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Benign_familial_hematuria": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 15,
    "Benign_familial_hematuria|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases": 1,
    "Microscopic_hematuria": 2,
    "Alport_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "COL4A4-related_disorder|not_provided": 12,
    "not_provided|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 28,
    "Inborn_genetic_diseases|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 2,
    "not_provided|Autosomal_dominant_Alport_syndrome": 14,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|COL4A4-related_disorder|not_specified|not_provided|Alport_syndrome": 1,
    "not_specified|COL4A4-related_disorder|not_provided|Alport_syndrome": 1,
    "not_provided|COL4A4-related_disorder|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome": 137,
    "Kidney_disorder|not_provided|Alport_syndrome": 2,
    "COL4A4-related_disorder": 25,
    "Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_dominant_Alport_syndrome|not_provided|COL4A4-related_disorder": 1,
    "COL4A4-related_disorder|Alport_syndrome|Inborn_genetic_diseases|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Kidney_disorder|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome": 3,
    "Meniere_disease|Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome": 46,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 3,
    "not_specified|not_provided|Alport_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "not_specified|not_provided|Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|COL4A4-related_disorder": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Chronic_kidney_disease": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_dominant_Alport_syndrome": 2,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided": 7,
    "not_specified|Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 3,
    "COL4A4-related_disorder|not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 3,
    "not_specified|Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 5,
    "Meniere_disease|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 2,
    "Disease_of_glomerular_basement_membrane": 2,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome|not_provided": 3,
    "Kidney_disorder|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Hematuria|_benign_familial|_1": 12,
    "Inborn_genetic_diseases|COL4A4-related_disorder": 1,
    "Haematuria|not_provided": 2,
    "Autosomal_recessive_Alport_syndrome|Kidney_disorder|Alport_syndrome|Hematuria|_benign_familial|_1|Focal_segmental_glomerulosclerosis|Benign_familial_hematuria|not_provided": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|COL4A4-related_disorder": 1,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Hematuria|_benign_familial|_1|Myopia|Proteinuria|Hypertensive_disorder|Hearing_impairment|Hematuria|not_provided": 1,
    "Benign_familial_hematuria|COL4A4-related_disorder": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|not_specified|Alport_syndrome|COL4A4-related_disorder": 1,
    "Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 6,
    "Autosomal_recessive_Alport_syndrome|not_provided|Hematuria|_benign_familial|_1": 6,
    "not_specified|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 4,
    "Autosomal_recessive_Alport_syndrome|COL4A4-related_disorder|Alport_syndrome|not_specified": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Alport_syndrome|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_specified": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Inborn_genetic_diseases|not_provided": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome": 3,
    "not_provided|Hypertensive_disorder|Hyperkalemia|Thrombocytopenia|Stage_5_chronic_kidney_disease|not_specified|Alport_syndrome": 1,
    "not_provided|not_specified|Autosomal_recessive_Alport_syndrome": 5,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_specified|not_provided": 1,
    "not_provided|Alport_syndrome|COL4A4-related_disorder|not_specified": 1,
    "COL4A4-related_disorder|not_provided|Kidney_disorder|Alport_syndrome": 1,
    "Benign_familial_hematuria|not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "not_specified|See_cases|Autosomal_recessive_Alport_syndrome": 1,
    "COL4A4-related_disorder|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Kidney_damage": 1,
    "not_specified|Alport_syndrome": 3,
    "Autosomal_recessive_Alport_syndrome|not_specified|not_provided": 3,
    "not_provided|not_specified|Alport_syndrome": 5,
    "not_provided|Benign_familial_hematuria": 6,
    "not_specified|Alport_syndrome|not_provided|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_Alport_syndrome": 3,
    "not_specified|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Inborn_genetic_diseases|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 10,
    "not_specified|Kidney_disorder|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome|not_specified": 1,
    "COL4A4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Alport_syndrome|not_provided|not_specified": 3,
    "not_specified|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|X-linked_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases": 2,
    "not_specified|Autosomal_recessive_Alport_syndrome|not_provided": 3,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Inborn_genetic_diseases|not_provided|Alport_syndrome": 1,
    "Alport_syndrome|Kidney_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome_type_2|not_provided|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Inborn_genetic_diseases": 3,
    "COL4A4-related_disorder|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Benign_familial_hematuria|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_Alport_syndrome": 6,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_Alport_syndrome": 1,
    "Alport_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "COL4A4-related_disorder|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 1,
    "COL4A4-related_disorder|Disease_of_glomerular_basement_membrane|Focal_segmental_glomerulosclerosis|not_provided|Inborn_genetic_diseases|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder": 2,
    "not_specified|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified": 1,
    "Hematuria": 4,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 2,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided|COL4A4-related_disorder": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 3,
    "COL4A4-related_disorder|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_specified|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Porencephaly_2": 1,
    "Alport_syndrome|Focal_segmental_glomerulosclerosis|not_specified|not_provided": 2,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Inborn_genetic_diseases": 4,
    "COL4A4-related_disorder|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome|Meniere_disease": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 5,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|not_specified": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|COL4A4-related_disorder|not_provided": 2,
    "not_provided|COL4A4-related_disorder|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 1,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|not_specified": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Benign_familial_hematuria": 3,
    "Focal_segmental_glomerulosclerosis|Alport_syndrome|not_specified|not_provided": 1,
    "Kidney_disorder|Alport_syndrome|not_specified|not_provided": 1,
    "COL4A4-related_disorder|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 4,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome": 3,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases": 5,
    "not_specified|Alport_syndrome|not_provided": 7,
    "Hypertensive_disorder|Thrombocytopenia|Stage_5_chronic_kidney_disease|Hyperkalemia": 1,
    "Benign_familial_hematuria|not_provided": 2,
    "not_provided|Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 3,
    "COL4A4-related_disorder|not_provided|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Alport_syndrome": 1,
    "Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder": 1,
    "Inborn_genetic_diseases|Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome|Benign_familial_hematuria|not_provided": 1,
    "Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|not_specified": 1,
    "COL4A4-related_disorder|not_specified|Atypical_hemolytic-uremic_syndrome|not_provided|Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|Benign_familial_hematuria": 1,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome|COL4A4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|not_provided": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided|Inborn_genetic_diseases": 1,
    "Alport_syndrome|not_specified|Kidney_disorder|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Hematuria|_benign_familial|_1|COL4A4-related_disorder|not_provided|Inborn_genetic_diseases|Alport_syndrome|Chronic_kidney_disease": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Focal_segmental_glomerulosclerosis|not_provided|Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 2,
    "not_provided|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 2,
    "not_specified|not_provided|Alport_syndrome": 7,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified|Autosomal_dominant_Alport_syndrome": 1,
    "COL4A4-related_disorder|not_provided|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "COL4A4-related_disorder|not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Benign_familial_hematuria|not_provided|Alport_syndrome|not_specified": 1,
    "Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|not_specified|not_provided|Autosomal_recessive_Alport_syndrome|Focal_segmental_glomerulosclerosis|Alport_syndrome": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided|Benign_familial_hematuria": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Hematuria|_benign_familial|_1|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|Alport_syndrome": 2,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|Glomerulonephritis|Alport_syndrome": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "not_provided|Benign_familial_hematuria|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|COL4A4-related_disorder": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Inborn_genetic_diseases|Alport_syndrome": 1,
    "Alport_syndrome|not_provided|Inborn_genetic_diseases|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 1,
    "not_provided|Kidney_disorder|Alport_syndrome|not_specified": 1,
    "Alport_syndrome|not_specified|not_provided": 8,
    "Benign_familial_hematuria|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 1,
    "Polycystic_kidney_disease": 195,
    "Alport_syndrome|not_provided|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "not_provided|Proteinuria|Hematuria|Hypertensive_disorder|Hearing_impairment|Myopia|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome|Benign_familial_hematuria": 1,
    "not_provided|Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|COL4A4-related_disorder": 1,
    "Alport_syndrome|not_specified": 6,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome|not_provided": 3,
    "not_specified|Alport_syndrome|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "Hematuria|_benign_familial|_1|not_provided|COL4A4-related_disorder|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|Benign_familial_hematuria": 1,
    "not_provided|Alport_syndrome|not_specified": 5,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|COL4A4-related_disorder|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|COL4A4-related_disorder": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|not_provided": 2,
    "not_provided|Alport_syndrome|COL4A4-related_disorder": 3,
    "Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_specified|Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 3,
    "Alport_syndrome|not_provided|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 1,
    "not_provided|not_specified|COL4A4-related_disorder": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|not_specified|Alport_syndrome": 1,
    "not_provided|Alport_syndrome|not_specified|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|Benign_familial_hematuria|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome": 1,
    "not_specified|Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|Kidney_disorder": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 5,
    "Focal_segmental_glomerulosclerosis|Alport_syndrome|not_provided|not_specified": 2,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|COL4A4-related_disorder|Inborn_genetic_diseases|Alport_syndrome|not_provided": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Kidney_disorder|not_specified|Alport_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 1,
    "Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome|not_specified|Autosomal_dominant_Alport_syndrome|Inborn_genetic_diseases": 1,
    "Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 2,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome|Nephrotic_syndrome": 1,
    "not_specified|Alport_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome": 2,
    "not_provided|COL4A4-related_disorder|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 2,
    "Alport_syndrome|COL4A4-related_disorder|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 4,
    "not_provided|Alport_syndrome|Haematuria|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|not_provided": 3,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 3,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|not_specified|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "not_specified|COL4A4-related_disorder|not_provided": 1,
    "Glomerulonephritis|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|not_provided|Alport_syndrome": 2,
    "COL4A4-related_disorder|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Alport_syndrome|not_provided|COL4A4-related_disorder": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided|not_specified": 1,
    "not_specified|Alport_syndrome|not_provided|Kidney_disorder": 1,
    "not_specified|Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|Benign_familial_hematuria|not_provided": 1,
    "COL4A4-related_disorder|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|Microscopic_hematuria": 1,
    "Meniere_disease|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_specified|Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder|not_provided": 1,
    "Nephrotic_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Hematuria|_benign_familial|_1|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|not_specified|Focal_segmental_glomerulosclerosis": 1,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 2,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_specified|not_provided|Alport_syndrome": 1,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|COL4A4-related_disorder": 1,
    "Hematuria|_benign_familial|_1|Alport_syndrome|not_provided": 1,
    "COL4A4-related_disorder|Alport_syndrome|not_provided": 2,
    "not_provided|Glomerulonephritis": 2,
    "not_provided|Autosomal_recessive_Alport_syndrome|not_specified": 7,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Hematuria|_benign_familial|_1": 1,
    "not_specified|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Alport_syndrome|not_provided|Benign_familial_hematuria|COL4A4-related_disorder": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Inborn_genetic_diseases": 1,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|COL4A4-related_disorder|not_provided": 1,
    "not_specified|not_provided|Alport_syndrome|Kidney_disorder": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|Hematuria|_benign_familial|_1": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome|not_provided": 2,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Hematuria|_benign_familial|_1|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome|COL4A4-related_disorder|not_provided": 1,
    "not_provided|COL4A4-related_disorder|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|not_provided": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 16,
    "not_provided|Alport_syndrome|Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Alport_syndrome|Autosomal_dominant_Alport_syndrome": 5,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Alport_syndrome|Diffuse_mesangial_sclerosis|not_provided": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1": 1,
    "Alport_syndrome|Inborn_genetic_diseases": 5,
    "not_provided|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified": 1,
    "not_provided|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Alport_syndrome|Kidney_disorder|not_provided|not_specified": 1,
    "Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|COL4A4-related_disorder": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_1|Benign_familial_hematuria": 1,
    "not_provided|Hematuria|_benign_familial|_1": 2,
    "Microscopic_hematuria|Inborn_genetic_diseases|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Hematuria": 1,
    "Hematuria|_benign_familial|_1|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 1,
    "Benign_familial_hematuria|Hematuria|_benign_familial|_1": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Alport_syndrome": 2,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Alport_syndrome": 1,
    "not_specified|COL4A3-related_disorder|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "COL4A3-related_disorder": 24,
    "Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Inborn_genetic_diseases|not_provided|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 2,
    "not_specified|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Inborn_genetic_diseases|COL4A3-related_disorder|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided|COL4A3-related_disorder|not_specified": 1,
    "COL4A3-related_disorder|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 2,
    "COL4A3-related_disorder|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 2,
    "not_provided|not_specified|Alport_syndrome|Kidney_disorder": 1,
    "Focal_segmental_glomerulosclerosis|not_provided|not_specified|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided|Alport_syndrome": 2,
    "COL4A3-related_disorder|Alport_syndrome|Autosomal_dominant_Alport_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 181,
    "not_provided|Autosomal_dominant_Alport_syndrome|COL4A3-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Alport_syndrome|not_specified|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive": 21,
    "not_specified|not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|COL4A3-related_disorder|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_specified|not_provided|COL4A3-related_disorder|Alport_syndrome": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|COL4A3-related_disorder": 1,
    "not_specified|not_provided|COL4A3-related_disorder|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 3,
    "Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 26,
    "not_specified|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|COL4A3-related_disorder": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Autosomal_dominant_Alport_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|COL4A3-related_disorder|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Alport_syndrome": 2,
    "not_provided|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 7,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided": 3,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided": 17,
    "not_provided|COL4A3-related_disorder|Alport_syndrome": 2,
    "not_provided|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 12,
    "not_specified|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 9,
    "not_specified|Autosomal_recessive_Alport_syndrome": 2,
    "COL4A3-related_disorder|not_provided": 11,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided|COL4A3-related_disorder": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided": 8,
    "not_specified|Alport_syndrome|Focal_segmental_glomerulosclerosis|not_provided|Chronic_kidney_disease": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Alport_syndrome|Inborn_genetic_diseases|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Hereditary_hearing_loss_and_deafness": 2,
    "not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|not_provided": 3,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided|Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Alport_syndrome|not_provided|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "Autosomal_dominant_Alport_syndrome|not_specified|Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided|Kidney_disorder": 1,
    "COL4A3-related_disorder|not_provided|Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|COL4A3-related_disorder|not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Hematuria|_benign_familial|_2": 1,
    "not_provided|Alport_syndrome_3b|_autosomal_recessive": 3,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome": 3,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome|not_provided": 2,
    "COL4A3-related_disorder|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|not_provided|Alport_syndrome": 2,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome|not_specified|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified|Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_dominant_Alport_syndrome|not_provided": 2,
    "COL4A3-related_disorder|Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided": 1,
    "COL4A3-related_disorder|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Alport_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Alport_syndrome|not_provided|not_specified|Atypical_hemolytic-uremic_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "not_provided|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 4,
    "COL4A3-related_disorder|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 2,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 2,
    "Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided": 2,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome|Autosomal_dominant_Alport_syndrome|not_provided": 1,
    "COL4A3-related_disorder|not_provided|not_specified|Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|COL4A3-related_disorder": 1,
    "Alport_syndrome|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 5,
    "not_provided|Alport_syndrome|COL4A3-related_disorder": 1,
    "Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|not_provided": 2,
    "Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "Autosomal_recessive_Alport_syndrome|not_specified|Autosomal_dominant_Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome": 2,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|not_specified": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Nephrotic_syndrome|not_specified|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome|Benign_familial_hematuria|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Benign_familial_hematuria": 1,
    "not_provided|COL4A3-related_disorder|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive|not_provided": 3,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 3,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 10,
    "COL4A3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Benign_familial_hematuria": 1,
    "Alport_syndrome|not_provided|not_specified|Autosomal_recessive_Alport_syndrome": 1,
    "COL4A3-related_disorder|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Inborn_genetic_diseases|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided": 12,
    "not_specified|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 1,
    "Autosomal_recessive_Alport_syndrome|not_specified|Alport_syndrome|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|COL4A3-related_disorder": 1,
    "not_provided|not_specified|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 17,
    "not_provided|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome": 2,
    "not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome": 1,
    "Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_specified": 1,
    "not_provided|Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|COL4A3-related_disorder": 1,
    "Benign_familial_hematuria|not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided": 2,
    "Autosomal_dominant_Alport_syndrome|not_specified|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|COL4A3-related_disorder": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|COL4A3-related_disorder|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|not_provided|not_specified|Alport_syndrome": 2,
    "Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|not_provided|Alport_syndrome_3b|_autosomal_recessive|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Hearing_impairment|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|Autosomal_recessive_Alport_syndrome": 3,
    "Focal_segmental_glomerulosclerosis|Autosomal_recessive_Alport_syndrome|not_specified|Alport_syndrome|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|COL4A3-related_disorder|not_specified": 1,
    "not_specified|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 1,
    "not_provided|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|COL4A3-related_disorder|Alport_syndrome": 1,
    "Alport_syndrome|not_provided|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_provided": 3,
    "not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Alport_syndrome": 1,
    "Haematuria|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome|Alport_syndrome|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified|Alport_syndrome|not_provided": 1,
    "COL4A3-related_disorder|Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "COL4A3-related_disorder|Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_specified|COL4A3-related_disorder": 1,
    "COL4A3-related_disorder|not_specified": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided|Alport_syndrome": 2,
    "Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_specified|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome|not_provided": 2,
    "not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Benign_familial_hematuria|not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Autosomal_recessive_Alport_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 3,
    "not_provided|Autosomal_recessive_Alport_syndrome|COL4A3-related_disorder|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 2,
    "COL4A3-related_disorder|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "COL4A3-related_disorder|Inborn_genetic_diseases|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 1,
    "COL4A3-related_disorder|not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_specified|Autosomal_recessive_Alport_syndrome": 1,
    "COL4A3-related_disorder|Chronic_kidney_disease|Inborn_genetic_diseases|not_specified|not_provided|Alport_syndrome": 1,
    "COL4A3-related_disorder|Alport_syndrome_3b|_autosomal_recessive|not_provided|not_specified": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Microscopic_hematuria|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "not_provided|not_specified|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 2,
    "not_provided|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Alport_syndrome": 1,
    "Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|not_specified": 1,
    "COL4A3-related_disorder|Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Kidney_disorder|not_specified|Benign_familial_hematuria": 1,
    "not_specified|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|COL4A3-related_disorder": 9,
    "Inborn_genetic_diseases|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_provided": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|COL4A3-related_disorder|not_provided": 1,
    "not_provided|Hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria": 1,
    "Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|COL4A3-related_disorder": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|COL4A3-related_disorder|Autosomal_recessive_Alport_syndrome": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|not_specified": 1,
    "COL4A3-related_disorder|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 3,
    "Kidney_disorder|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_specified|not_provided|Benign_familial_hematuria": 1,
    "Autosomal_dominant_Alport_syndrome|not_provided|COL4A3-related_disorder": 1,
    "not_provided|COL4A3-related_disorder|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Autosomal_recessive_Alport_syndrome|Nephrotic_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Kidney_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hematuria|Glomerulopathy": 1,
    "Inborn_genetic_diseases|not_provided|Alport_syndrome": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|COL4A3-related_disorder": 1,
    "not_provided|Hereditary_disease": 1,
    "not_provided|not_specified|Alport_syndrome|Atypical_hemolytic-uremic_syndrome": 1,
    "Hematuria|not_provided": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_provided|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome": 1,
    "Alport_syndrome|Benign_familial_hematuria|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Alport_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|COL4A3-related_disorder": 1,
    "Autosomal_dominant_Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided|Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 2,
    "Alport_syndrome|not_provided|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 3,
    "not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|not_provided|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_specified|not_provided": 1,
    "COL4A3-related_disorder|not_specified|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome|not_provided": 3,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided|Inborn_genetic_diseases|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "not_provided|Inborn_genetic_diseases|Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_specified|Hearing_impairment": 1,
    "not_provided|COL4A3-related_disorder|Alport_syndrome_3b|_autosomal_recessive|Inborn_genetic_diseases|not_specified|Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_recessive_Alport_syndrome": 1,
    "COL4A3-related_disorder|not_specified|Kidney_disorder|not_provided|Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "not_provided|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Stickler_syndrome|not_provided": 1,
    "Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Alport_syndrome|not_specified|Autosomal_dominant_Alport_syndrome|COL4A3-related_disorder": 1,
    "not_provided|not_specified|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 1,
    "Alport_syndrome|Macroscopic_hematuria|Moderate_albuminuria|Microscopic_hematuria|Proteinuria|COL4A3-related_disorder|not_provided|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2": 1,
    "COL4A3-related_disorder|Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|Pilarowski-Bjornsson_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Inborn_genetic_diseases": 1,
    "Alport_syndrome|not_provided|See_cases": 1,
    "Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_provided|COL4A3-related_disorder": 1,
    "Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Kidney_disorder|not_specified|not_provided|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_provided|COL4A3-related_disorder|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|not_provided|Alport_syndrome": 1,
    "COL4A3-related_disorder|not_specified|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_provided|Alport_syndrome": 1,
    "COL4A3-related_disorder|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_provided": 2,
    "not_specified|Alport_syndrome|Atypical_hemolytic-uremic_syndrome|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "not_specified|Autosomal_dominant_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "not_provided|COL4A3-related_disorder|Alport_syndrome_3b|_autosomal_recessive|focal_and_segmental_glomerulosclerosis|not_specified|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_specified": 1,
    "not_specified|not_provided|Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Haematuria|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|Alport_syndrome|not_specified|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Benign_familial_hematuria|not_provided|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|Benign_familial_hematuria|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Autosomal_dominant_Alport_syndrome|Collagen_IV-related_nephropathies": 1,
    "Autosomal_dominant_Alport_syndrome|COL4A3-related_disorder|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|not_provided": 2,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Inborn_genetic_diseases|Alport_syndrome|not_provided": 1,
    "Autosomal_recessive_Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "COL4A3-related_disorder|not_specified|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|not_provided|Alport_syndrome|Hearing_impairment": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome": 1,
    "Alport_syndrome|COL4A3-related_disorder|not_specified|Autosomal_dominant_Alport_syndrome|Kidney_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Alport_syndrome|not_provided": 1,
    "not_specified|Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome": 1,
    "Kidney_disorder|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_specified|not_provided|Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Alport_syndrome|Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|not_specified|not_provided": 1,
    "not_specified|Alport_syndrome|not_provided|Autosomal_recessive_Alport_syndrome|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided": 1,
    "COL4A3-related_disorder|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria": 1,
    "Autosomal_recessive_Alport_syndrome|Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Osteogenesis_imperfecta|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|COL4A3-related_disorder": 1,
    "Chronic_kidney_disease|COL4A3-related_disorder|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome|Autosomal_recessive_Alport_syndrome|Inborn_genetic_diseases|not_provided|Alport_syndrome": 1,
    "not_specified|Kidney_disorder|not_provided|Alport_syndrome": 1,
    "Autosomal_recessive_Alport_syndrome|not_specified": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|Alport_syndrome|not_provided": 1,
    "Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive|not_specified|not_provided|Autosomal_recessive_Alport_syndrome": 1,
    "Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Hematuria|_benign_familial|_2|Autosomal_dominant_Alport_syndrome|Alport_syndrome_3b|_autosomal_recessive|COL4A3-related_disorder|not_provided": 1,
    "not_specified|Alport_syndrome|not_provided|Autosomal_dominant_Alport_syndrome": 1,
    "not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|Benign_familial_hematuria|Autosomal_dominant_Alport_syndrome": 1,
    "not_specified|Alport_syndrome_3b|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Alport_syndrome|not_provided|Alport_syndrome|Hematuria|_benign_familial|_2|Alport_syndrome_3b|_autosomal_recessive": 1,
    "Alport_syndrome_3b|_autosomal_recessive|Autosomal_dominant_Alport_syndrome|Hematuria|_benign_familial|_2|COL4A3-related_disorder|Benign_familial_hematuria|Autosomal_recessive_Alport_syndrome|not_provided|Alport_syndrome": 1,
    "Autosomal_dominant_Alport_syndrome|COL4A3-related_disorder|not_provided|Alport_syndrome|Autosomal_recessive_Alport_syndrome|not_specified": 1,
    "Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2": 11,
    "MFF-related_disorder": 2,
    "not_provided|Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2": 1,
    "Global_developmental_delay|Mitochondrial_encephalomyopathy|Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2": 1,
    "Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MFF-related_disorder|not_specified": 1,
    "Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2|not_provided": 1,
    "MFF-related_disorder|not_provided": 1,
    "not_provided|Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2|not_specified": 1,
    "not_provided|MFF-related_disorder": 1,
    "Inborn_genetic_diseases|Encephalopathy_due_to_defective_mitochondrial_and_peroxisomal_fission_2|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|MFF-related_disorder|not_provided": 1,
    "not_provided|TM4SF20-related_disorder": 5,
    "TM4SF20-related_disorder": 2,
    "Specific_language_impairment_5": 3,
    "not_specified|Specific_language_impairment_5": 1,
    "TM4SF20-related_disorder|not_provided": 2,
    "Biotin-responsive_basal_ganglia_disease": 457,
    "Biotin-responsive_basal_ganglia_disease|not_provided": 35,
    "Thiamine_Metabolism_Dysfunction_Syndrome": 3,
    "not_provided|Biotin-responsive_basal_ganglia_disease": 54,
    "Thiamine_Metabolism_Dysfunction_Syndrome|not_provided|Biotin-responsive_basal_ganglia_disease": 2,
    "not_specified|not_provided|Biotin-responsive_basal_ganglia_disease": 12,
    "Biotin-responsive_basal_ganglia_disease|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|SLC19A3-related_disorder|Biotin-responsive_basal_ganglia_disease": 1,
    "Inborn_genetic_diseases|not_provided|Biotin-responsive_basal_ganglia_disease": 4,
    "Biotin-responsive_basal_ganglia_disease|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Biotin-responsive_basal_ganglia_disease": 9,
    "SLC19A3-related_disorder": 1,
    "SLC19A3-related_disorder|Biotin-responsive_basal_ganglia_disease": 1,
    "Thiamine_metabolism_dysfunction_syndrome_2_(biotin/thiamine-responsive_basal_ganglia_disease_type)|Inborn_genetic_diseases|not_provided|Biotin-responsive_basal_ganglia_disease": 1,
    "Biotin-responsive_basal_ganglia_disease|SLC19A3-related_disorder|not_provided": 1,
    "not_provided|Biotin-responsive_basal_ganglia_disease|See_cases": 1,
    "SLC19A3-related_disorder|not_provided|Biotin-responsive_basal_ganglia_disease": 4,
    "Thiamine_Metabolism_Dysfunction_Syndrome|not_specified|not_provided|Biotin-responsive_basal_ganglia_disease": 1,
    "Biotin-responsive_basal_ganglia_disease|not_specified": 3,
    "not_specified|Biotin-responsive_basal_ganglia_disease": 5,
    "Biotin-responsive_basal_ganglia_disease|not_provided|Inborn_genetic_diseases": 1,
    "Biotin-responsive_basal_ganglia_disease|SLC19A3-related_disorder": 1,
    "Biotin-responsive_basal_ganglia_disease|SLC19A3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|not_provided|Inborn_genetic_diseases|not_specified|Biotin-responsive_basal_ganglia_disease": 1,
    "not_provided|not_specified|Biotin-responsive_basal_ganglia_disease": 2,
    "not_provided|SLC19A3-related_disorder|Biotin-responsive_basal_ganglia_disease": 1,
    "SLC19A3-related_disorder|not_specified|not_provided|Biotin-responsive_basal_ganglia_disease": 1,
    "not_provided|Thiamine_Metabolism_Dysfunction_Syndrome": 1,
    "DAW1-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Ciliary_dyskinesia|_primary|_52": 4,
    "Ciliary_dyskinesia|_primary|_52": 1,
    "not_specified|DAW1-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_52|Primary_ciliary_dyskinesia": 1,
    "PID1-related_disorder": 2,
    "not_provided|TRIP12-related_disorder": 5,
    "Clark-Baraitser_syndrome": 97,
    "TRIP12-related_disorder": 31,
    "TRIP12-related_disorder|Inborn_genetic_diseases": 2,
    "Clark-Baraitser_syndrome|not_provided": 9,
    "TRIP12-related_disorder|not_provided": 2,
    "not_provided|Clark-Baraitser_syndrome": 8,
    "Self-limited_familial_infantile_epilepsy": 1,
    "Clark-Baraitser_syndrome|Inborn_genetic_diseases|not_provided|See_cases": 1,
    "Intellectual_disability|Clark-Baraitser_syndrome": 1,
    "Clark-Baraitser_syndrome|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Clark-Baraitser_syndrome": 1,
    "Clark-Baraitser_syndrome|Inborn_genetic_diseases": 5,
    "TRIP12-related_disorder|Clark-Baraitser_syndrome|not_provided": 1,
    "Clark-Baraitser_syndrome|Inborn_genetic_diseases|not_provided|TRIP12-related_disorder": 1,
    "TRIP12_associated_autism_with_facial_dysmorphology": 1,
    "not_provided|Inborn_genetic_diseases|Clark-Baraitser_syndrome": 1,
    "not_provided|Clark-Baraitser_syndrome|Inborn_genetic_diseases": 1,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 362,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|not_provided": 4,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Mycobacterium_tuberculosis|_susceptibility_to": 11,
    "Inborn_genetic_diseases|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 23,
    "SP110-related_disorder|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 3,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Inborn_genetic_diseases": 20,
    "not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|SP110-related_disorder": 1,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|not_specified|not_provided": 3,
    "not_specified|not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 2,
    "not_specified|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|not_provided": 4,
    "not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 7,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|SP110-related_disorder": 4,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|SP110-related_disorder|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Inborn_genetic_diseases": 2,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Mycobacterium_tuberculosis|_susceptibility_to|not_provided|SP110-related_disorder": 1,
    "not_specified|not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "SP110-related_disorder": 2,
    "not_provided|not_specified|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 1,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|SP110-related_disorder|Mycobacterium_tuberculosis|_susceptibility_to|not_provided": 1,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|Mycobacterium_tuberculosis|_susceptibility_to|SP110-related_disorder": 1,
    "not_specified|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 1,
    "not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|not_specified": 1,
    "Hepatic_veno-occlusive_disease-immunodeficiency_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hepatic_veno-occlusive_disease-immunodeficiency_syndrome": 1,
    "Joubert_syndrome_30": 4,
    "not_provided|ARMC9-related_disorder": 11,
    "Joubert_syndrome|Joubert_syndrome_30|ARMC9-related_Joubert_syndrome": 4,
    "ARMC9-related_disorder": 5,
    "not_provided|Joubert_syndrome_30": 6,
    "Joubert_syndrome_30|ARMC9-related_Joubert_syndrome|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_30|not_provided|ARMC9-related_Joubert_syndrome": 1,
    "ARMC9-related_disorder|not_provided": 7,
    "Joubert_syndrome_30|See_cases|not_provided": 1,
    "Diabetes_mellitus|Corpus_callosum|_agenesis_of|not_provided": 1,
    "Joubert_syndrome_30|not_provided": 7,
    "Joubert_syndrome_30|ARMC9-related_Joubert_syndrome|Dandy-Walker_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome_30|ARMC9-related_Joubert_syndrome": 1,
    "Joubert_syndrome_30|ARMC9-related_Joubert_syndrome|Joubert_syndrome": 1,
    "not_specified|Joubert_syndrome_30|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|ARMC9-related_disorder": 1,
    "Dandy-Walker_syndrome|not_provided|Joubert_syndrome_30|ARMC9-related_Joubert_syndrome|Joubert_syndrome": 1,
    "ARMC9-related_Joubert_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_30|not_provided": 1,
    "not_specified|See_cases": 13,
    "Joubert_syndrome_22": 53,
    "not_provided|Joubert_syndrome_22": 2,
    "PDE6D-related_disorder|Joubert_syndrome_22": 1,
    "Joubert_syndrome_22|not_provided": 1,
    "Joubert_syndrome_22|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_22|PDE6D-related_disorder": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_22": 1,
    "Perlman_syndrome": 1945,
    "not_provided|not_specified|Perlman_syndrome": 1,
    "Perlman_syndrome|DIS3L2-related_disorder": 27,
    "Inborn_genetic_diseases|Perlman_syndrome": 51,
    "not_provided|Perlman_syndrome": 37,
    "Perlman_syndrome|Inborn_genetic_diseases": 30,
    "Perlman_syndrome|not_provided|DIS3L2-related_disorder|Inborn_genetic_diseases": 1,
    "Perlman_syndrome|not_provided": 29,
    "not_provided|Perlman_syndrome|Inborn_genetic_diseases": 2,
    "DIS3L2-related_disorder": 6,
    "not_provided|Perlman_syndrome|DIS3L2-related_disorder": 8,
    "Perlman_syndrome|not_provided|not_specified": 2,
    "Perlman_syndrome|DIS3L2-related_disorder|not_provided": 6,
    "Perlman_syndrome|not_specified": 2,
    "Perlman_syndrome|DIS3L2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Perlman_syndrome": 2,
    "not_provided|Perlman_syndrome|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|Perlman_syndrome": 6,
    "DIS3L2-related_disorder|Perlman_syndrome": 14,
    "Perlman_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Perlman_syndrome|not_provided|DIS3L2-related_disorder": 1,
    "Perlman_syndrome|not_specified|not_provided": 3,
    "DIS3L2-related_disorder|not_provided": 1,
    "Perlman_syndrome|not_specified|not_provided|DIS3L2-related_disorder": 1,
    "Inborn_genetic_diseases|Perlman_syndrome|DIS3L2-related_disorder": 1,
    "DIS3L2-related_disorder|Inborn_genetic_diseases|Perlman_syndrome": 1,
    "DIS3L2-related_disorder|not_provided|Perlman_syndrome": 1,
    "Perlman_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Perlman_syndrome": 1,
    "DIS3L2-related_disorder|Perlman_syndrome|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Perlman_syndrome": 1,
    "Perlman_syndrome|DIS3L2-related_disorder|Inborn_genetic_diseases": 1,
    "Nephroblastoma": 6,
    "Perlman_syndrome|Hepatoblastoma": 1,
    "not_provided|Perlman_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Perlman_syndrome|DIS3L2-related_disorder": 1,
    "not_provided|DIS3L2-related_disorder": 1,
    "ALKALINE_PHOSPHATASE|_PLACENTAL|_ALLELE-1_POLYMORPHISM": 1,
    "ALKALINE_PHOSPHATASE|_PLACENTAL|_ALLELE-3_POLYMORPHISM|not_provided": 1,
    "ALPI-related_disorder": 24,
    "not_specified|ALPI-related_disorder": 2,
    "ALPI-related_disorder|not_provided": 1,
    "ALPI-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Distal_arthrogryposis_type_5D|not_provided": 1,
    "Distal_arthrogryposis_type_5D": 55,
    "Distal_arthrogryposis_type_5D|not_provided": 7,
    "ECEL1-related_disorder": 11,
    "Arthrogryposis_multiplex_congenita": 3,
    "ECEL1-related_disorder|not_provided": 5,
    "not_provided|Distal_arthrogryposis_type_5D": 7,
    "ECEL1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Distal_arthrogryposis_type_5D": 1,
    "Distal_arthrogryposis_type_5D|Inborn_genetic_diseases": 4,
    "ECEL1-related_disorder|not_specified|not_provided": 2,
    "Distal_arthrogryposis": 10,
    "not_provided|Distal_arthrogryposis_type_5D|See_cases": 1,
    "See_cases|Distal_arthrogryposis_type_5D": 1,
    "Arthrogryposis": 2,
    "See_cases|Distal_arthrogryposis_type_5D|not_provided": 1,
    "not_provided|not_specified|Distal_arthrogryposis_type_5D": 1,
    "not_provided|ECEL1-related_disorder": 2,
    "Distal_arthrogryposis_type_5D|not_provided|Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita": 1,
    "Distal_arthrogryposis_type_5D|ECEL1-related_disorder|not_provided": 1,
    "Distal_arthrogryposis_type_5D|Inborn_genetic_diseases|not_provided": 1,
    "Isolated_microphthalmia_6": 74,
    "Isolated_microphthalmia_6|not_provided": 6,
    "not_provided|Isolated_microphthalmia_6": 7,
    "Inborn_genetic_diseases|Isolated_microphthalmia_6": 4,
    "not_provided|Isolated_microphthalmia_6|PRSS56-related_disorder": 1,
    "Isolated_microphthalmia_6|Inborn_genetic_diseases": 5,
    "PRSS56-related_disorder|not_provided": 1,
    "Isolated_microphthalmia_6|PRSS56-related_disorder": 1,
    "Nanophthalmia|PRSS56-related_disorder|not_provided|Isolated_microphthalmia_6": 1,
    "PRSS56-related_disorder": 2,
    "Isolated_microphthalmia_6|not_provided|Inborn_genetic_diseases": 1,
    "PRSS56-related_disorder|Isolated_microphthalmia_6": 1,
    "not_specified|Isolated_microphthalmia_6|not_provided": 1,
    "Congenital_myasthenic_syndrome_3A|not_provided": 1,
    "Congenital_myasthenic_syndrome_3B": 7,
    "Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome|CHRND-related_disorder": 1,
    "Congenital_myasthenic_syndrome_3B|Lethal_multiple_pterygium_syndrome": 4,
    "Congenital_myasthenic_syndrome_3A|not_provided|Lethal_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_3C|Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3B": 2,
    "Congenital_myasthenic_syndrome_3A|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_3B|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_3C|Congenital_myasthenic_syndrome_3A": 1,
    "Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|not_provided": 2,
    "not_specified|Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "Congenital_myasthenic_syndrome_3A|Lethal_multiple_pterygium_syndrome": 2,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_3B|Congenital_myasthenic_syndrome_3C|Congenital_myasthenic_syndrome_3A|not_provided": 1,
    "Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_3B": 2,
    "not_provided|Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome": 2,
    "CHRND-related_disorder|not_specified|Lethal_multiple_pterygium_syndrome": 1,
    "CHRND-related_disorder|Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "not_provided|Congenital_myasthenic_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "CHRND-related_disorder": 2,
    "Congenital_myasthenic_syndrome_3A|not_provided|Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome": 1,
    "CHRND-related_disorder|Lethal_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|CHRND-related_disorder": 4,
    "Lethal_multiple_pterygium_syndrome|CHRND-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome_3B|Lethal_multiple_pterygium_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3B|Congenital_myasthenic_syndrome_3C|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3C|Congenital_myasthenic_syndrome_3B": 1,
    "CHRND-related_disorder|not_provided|Lethal_multiple_pterygium_syndrome": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|CHRND-related_disorder": 1,
    "Congenital_myasthenic_syndrome_3C|not_provided|Lethal_multiple_pterygium_syndrome": 1,
    "Ptosis|Breathing_dysregulation|Muscle_weakness|Dyspnea": 2,
    "Congenital_myasthenic_syndrome_3B|Congenital_myasthenic_syndrome_3C|Lethal_multiple_pterygium_syndrome|not_provided": 2,
    "Centronuclear_myopathy|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3C": 1,
    "Congenital_myasthenic_syndrome_3C": 1,
    "Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3B|Congenital_myasthenic_syndrome_3C|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_3A": 2,
    "Lethal_multiple_pterygium_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Congenital_myasthenic_syndrome|not_provided|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_3A": 1,
    "Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3B|Congenital_myasthenic_syndrome_3C|Congenital_myasthenic_syndrome": 1,
    "Inborn_genetic_diseases|CHRND-related_disorder": 1,
    "Congenital_myasthenic_syndrome_3A|Congenital_myasthenic_syndrome_3B|Lethal_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome_3C|not_provided": 1,
    "Congenital_myasthenic_syndrome_3C|not_provided|Lethal_multiple_pterygium_syndrome|CHRND-related_disorder": 1,
    "CHRND-related_disorder|Congenital_myasthenic_syndrome|not_specified|not_provided|Lethal_multiple_pterygium_syndrome": 1,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Lethal_multiple_pterygium_syndrome|not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome": 3,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Autosomal_recessive_multiple_pterygium_syndrome": 2,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Congenital_myasthenic_syndrome": 2,
    "Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome": 16,
    "Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 3,
    "Ankle_flexion_contracture|Scoliosis|Arthrogryposis-like_hand_anomaly|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Autosomal_recessive_multiple_pterygium_syndrome": 11,
    "not_provided|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 12,
    "Lethal_multiple_pterygium_syndrome|CHRNG-related_disorder|not_provided|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|CHRNG-associated_hypo-akinesia_disorder_of_prenatal_onset|not_provided|Autosomal_recessive_multiple_pterygium_syndrome": 2,
    "Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "CHRNG-related_disorder|not_specified|not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|not_provided|Autosomal_recessive_multiple_pterygium_syndrome": 7,
    "Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome|not_provided": 3,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|not_provided": 10,
    "Autosomal_recessive_multiple_pterygium_syndrome|Inborn_genetic_diseases": 2,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 25,
    "not_provided|CHRNG-related_disorder": 3,
    "Ankle_flexion_contracture|Scoliosis|Arthrogryposis-like_hand_anomaly|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome|not_provided": 1,
    "not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome|Peripheral_neuropathy": 1,
    "Autosomal_recessive_multiple_pterygium_syndrome|not_provided": 3,
    "not_provided|Autosomal_recessive_multiple_pterygium_syndrome": 5,
    "Autosomal_recessive_multiple_pterygium_syndrome|Multiple_pterygium_syndrome|CHRNG-related_disorder|not_provided": 1,
    "CHRNG-related_disorder": 1,
    "Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|not_provided|not_specified|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "CHRNG-related_disorder|not_provided|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "not_specified|not_provided|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "not_provided|Autosomal_recessive_multiple_pterygium_syndrome|not_specified": 1,
    "CHRNG-associated_hypo-akinesia_disorder_of_prenatal_onset": 1,
    "not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome": 2,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "CHRNG-related_disorder|Inborn_genetic_diseases|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|not_provided|Abnormality_of_prenatal_development_or_birth": 1,
    "CHRNG-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Autosomal_recessive_multiple_pterygium_syndrome|not_provided|not_specified|Lethal_multiple_pterygium_syndrome": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|CHRNG-related_disorder|Autosomal_recessive_multiple_pterygium_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "not_specified|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome|not_provided|Rheumatoid_arthritis": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome": 2,
    "not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome|CHRNG-related_disorder": 1,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "CHRNG-associated_hypo-akinesia_disorder_of_prenatal_onset|not_provided|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "not_provided|not_specified|CHRNG-associated_hypo-akinesia_disorder_of_prenatal_onset|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|not_specified": 1,
    "Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome|not_specified|not_provided": 1,
    "CHRNG-related_disorder|not_provided|Autosomal_recessive_multiple_pterygium_syndrome|Lethal_multiple_pterygium_syndrome": 1,
    "CHRNG-related_disorder|Lethal_multiple_pterygium_syndrome|Autosomal_recessive_multiple_pterygium_syndrome": 1,
    "Parkinson_disease_11|_autosomal_dominant|_susceptibility_to": 10,
    "GIGYF2-related_disorder|Parkinson_disease_11|_autosomal_dominant|_susceptibility_to": 1,
    "GIGYF2-related_disorder": 23,
    "not_specified|Parkinson_disease_11|_autosomal_dominant|_susceptibility_to|GIGYF2-related_disorder|not_provided": 1,
    "Leber_congenital_amaurosis_16|not_provided": 3,
    "not_provided|Leber_congenital_amaurosis_16": 6,
    "Leber_congenital_amaurosis_16": 45,
    "Snowflake_vitreoretinal_degeneration|not_provided": 2,
    "not_specified|not_provided|Snowflake_vitreoretinal_degeneration|Leber_congenital_amaurosis_16": 1,
    "not_provided|Snowflake_vitreoretinal_degeneration": 1,
    "Snowflake_vitreoretinal_degeneration|Leber_congenital_amaurosis_16|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_16|not_provided|not_specified": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_16": 1,
    "Leber_congenital_amaurosis_16|Retinitis_pigmentosa": 1,
    "KCNJ13-related_condition": 1,
    "Snowflake_vitreoretinal_degeneration|Leber_congenital_amaurosis_16": 1,
    "not_specified|GIGYF2-related_disorder": 1,
    "GIGYF2-related_disorder|not_provided": 3,
    "Parkinson_disease_11|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "not_provided|GIGYF2-related_disorder": 3,
    "not_provided|Parkinson_disease_11|_autosomal_dominant|_susceptibility_to": 6,
    "not_specified|not_provided|Parkinson_disease_11|_autosomal_dominant|_susceptibility_to": 1,
    "ATG16L1-related_disorder": 5,
    "Inflammatory_bowel_disease_10": 2,
    "Inflammatory_bowel_disease_10|_susceptibility_to|not_provided|ATG16L1-related_disorder|not_specified": 1,
    "Retinitis_Pigmentosa|_Recessive|Oguchi_disease": 2,
    "Retinitis_pigmentosa|Oguchi_disease": 4,
    "Oguchi_disease|Retinitis_pigmentosa": 5,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa|SAG-related_disorder|Oguchi_disease": 1,
    "Oguchi_disease-1|Retinitis_pigmentosa_96|Retinitis_pigmentosa_47|not_provided": 1,
    "not_provided|SAG-related_disorder": 1,
    "Retinitis_pigmentosa|Oguchi_disease|not_provided": 6,
    "Retinitis_pigmentosa|not_provided|Oguchi_disease": 2,
    "SAG-related_disorder|not_provided": 7,
    "Oguchi_disease-1": 2,
    "not_provided|Retinitis_pigmentosa|Oguchi_disease": 6,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|Oguchi_disease|not_provided|Oguchi_disease-1|Retinitis_pigmentosa_47": 1,
    "SAG-related_disorder": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Oguchi_disease": 1,
    "Retinitis_pigmentosa|Oguchi_disease|Retinal_dystrophy|not_provided|not_specified": 1,
    "Oguchi_disease|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Oguchi_disease": 1,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Oguchi_disease": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_47|Oguchi_disease-1|Retinitis_pigmentosa_96": 1,
    "Retinitis_pigmentosa|not_specified|not_provided|Oguchi_disease": 1,
    "Oguchi_disease|not_provided": 1,
    "Retinitis_pigmentosa|Oguchi_disease|SAG-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_96|Oguchi_disease-1|Retinitis_pigmentosa_47": 1,
    "not_specified|Oguchi_disease-1|not_provided": 1,
    "not_provided|SAG-related_disorder|Retinitis_pigmentosa|Oguchi_disease": 1,
    "not_provided|Retinitis_pigmentosa|Oguchi_disease|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Oguchi_disease": 1,
    "not_provided|Oguchi_disease": 1,
    "Retinitis_pigmentosa|Oguchi_disease|not_provided|SAG-related_disorder": 1,
    "Oguchi_disease": 3,
    "not_provided|Oguchi_disease-1|Retinitis_pigmentosa_47|Retinal_dystrophy|Oguchi_disease|Oguchi_disease-2": 1,
    "not_provided|Oguchi_disease|SAG-related_disorder|not_specified|Retinitis_pigmentosa": 1,
    "Oguchi_disease-2": 18,
    "not_provided|Retinal_dystrophy|Oguchi_disease-1|Retinitis_pigmentosa_47": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_96|Oguchi_disease-1|Retinitis_pigmentosa_47|not_provided": 1,
    "Retinitis_pigmentosa_47|not_provided": 1,
    "not_provided|Oguchi_disease-1": 1,
    "Oguchi_disease|Inborn_genetic_diseases|Retinitis_pigmentosa|not_provided": 2,
    "SAG-related_disorder|Oguchi_disease-1|not_provided|Oguchi_disease": 1,
    "Oguchi_disease|Retinitis_pigmentosa|not_provided": 1,
    "Oguchi_disease|Retinitis_pigmentosa_47": 1,
    "Oguchi_disease|Retinitis_pigmentosa_47|SAG-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_provided|Oguchi_disease-1|not_specified|Oguchi_disease|Retinitis_pigmentosa_47|Retinitis_pigmentosa": 1,
    "SAG-related_disorder|Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Oguchi_disease|not_provided|Retinitis_pigmentosa": 1,
    "not_specified|Retinitis_pigmentosa|Oguchi_disease|not_provided": 1,
    "Retinal_dystrophy|not_provided|Oguchi_disease|Retinitis_pigmentosa|Oguchi_disease-1|Retinitis_pigmentosa_47": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Oguchi_disease|Oguchi_disease-1|not_provided|not_specified": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Oguchi_disease": 1,
    "DGKD-related_disorder|not_provided": 7,
    "DGKD-related_disorder|not_specified": 1,
    "DGKD-related_disorder": 8,
    "not_provided|DGKD-related_disorder": 4,
    "UGT1A9-related_disorder": 7,
    "UGT1A1-related_disorder": 29,
    "UGT1A9-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|UGT1A8-related_condition|not_provided|Gilbert_syndrome|_susceptibility_to|Gilbert_syndrome": 1,
    "Gilbert_syndrome|irinotecan_response_-_Toxicity": 1,
    "Lucey-Driscoll_syndrome": 3,
    "not_provided|UGT1A1-related_disorder": 11,
    "UGT1A1-related_disorder|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|not_provided|not_specified|Crigler-Najjar_syndrome|Irinotecan_response": 1,
    "not_specified|UGT1A1-related_disorder|Irinotecan_response|UGT1A9-related_disorder|not_provided": 1,
    "UGT1A9-related_disorder|not_provided|Irinotecan_response": 1,
    "not_provided|UGT1A1-related_disorder|Gilbert_syndrome": 1,
    "Irinotecan_response": 1,
    "UGT1A1-related_disorder|not_provided": 14,
    "not_provided|UGT1A4-related_disorder": 1,
    "Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1": 8,
    "Lucey-Driscoll_syndrome|Gilbert_syndrome|Crigler-Najjar_syndrome": 6,
    "Crigler-Najjar_syndrome|_type_II|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_provided": 3,
    "Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|UGT1A1-related_disorder|not_specified": 1,
    "not_provided|UGT1A1-related_disorder|Inborn_genetic_diseases": 2,
    "Crigler-Najjar_syndrome_type_1": 11,
    "Crigler-Najjar_syndrome|_type_II": 5,
    "Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome_type_1|not_provided": 1,
    "Hyperbilirubinemia": 4,
    "UGT1A1-related_disorder|Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|not_specified|not_provided|Crigler-Najjar_syndrome|Hyperbilirubinemia": 1,
    "Crigler-Najjar_syndrome|not_provided|Lucey-Driscoll_syndrome|Gilbert_syndrome": 3,
    "Crigler-Najjar_syndrome_type_1|Crigler-Najjar_syndrome|_type_II|Lucey-Driscoll_syndrome|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "Crigler-Najjar_syndrome|not_provided|UGT1A1-related_disorder|Gilbert_syndrome|Lucey-Driscoll_syndrome": 1,
    "Lucey-Driscoll_syndrome|not_provided": 1,
    "not_provided|Gilbert_syndrome": 4,
    "UGT1A1-related_disorder|Crigler-Najjar_syndrome|not_provided|Gilbert_syndrome|Lucey-Driscoll_syndrome": 1,
    "UGT1A1-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_specified|not_provided|Irinotecan_response": 1,
    "not_provided|Crigler-Najjar_syndrome": 1,
    "UGT1A1-related_disorder|Hyperbilirubinemia|not_provided": 1,
    "Crigler-Najjar_syndrome_type_1|Gilbert_syndrome": 1,
    "Crigler-Najjar_syndrome|not_provided|Gilbert_syndrome|Lucey-Driscoll_syndrome|UGT1A1-related_disorder": 1,
    "BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|not_provided": 1,
    "Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|not_provided": 1,
    "Hyperbilirubinemia|not_provided|Gilbert_syndrome|Crigler-Najjar_syndrome|_type_II|Inborn_genetic_diseases": 1,
    "not_provided|Gilbert_syndrome|UGT1A1-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome": 1,
    "UGT1A1-related_disorder|Inborn_genetic_diseases|not_provided|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome": 1,
    "Crigler-Najjar_syndrome|_type_II|not_provided": 1,
    "Crigler-Najjar_syndrome|Lucey-Driscoll_syndrome|Gilbert_syndrome": 7,
    "Gilbert_syndrome|Lucey-Driscoll_syndrome|not_provided|Crigler-Najjar_syndrome": 1,
    "Crigler-Najjar_syndrome_type_1|Hyperbilirubinemia": 1,
    "Gilbert_syndrome|Crigler-Najjar_syndrome|_type_II|Lucey-Driscoll_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome_type_1|UGT1A1-related_disorder|not_provided": 1,
    "BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1": 1,
    "not_specified|not_provided|Crigler-Najjar_syndrome|Gilbert_syndrome|Lucey-Driscoll_syndrome": 1,
    "Gilbert_syndrome|Lucey-Driscoll_syndrome|not_provided|Inborn_genetic_diseases|Crigler-Najjar_syndrome": 1,
    "not_provided|Lucey-Driscoll_syndrome|Gilbert_syndrome|Crigler-Najjar_syndrome|UGT1A1-related_disorder|Inborn_genetic_diseases": 1,
    "Crigler-Najjar_syndrome|not_provided": 3,
    "not_provided|Crigler-Najjar_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|UGT1A1-related_disorder|Inborn_genetic_diseases": 1,
    "Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|UGT1A1-related_disorder|not_provided": 1,
    "Crigler-Najjar_syndrome": 2,
    "UGT1A1-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Crigler-Najjar_syndrome|Hyperbilirubinemia": 1,
    "UGT1A1-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_specified|not_provided": 1,
    "Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_provided": 1,
    "Hyperbilirubinemia|Crigler-Najjar_syndrome_type_1|not_provided|UGT1A1-related_disorder": 1,
    "Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II": 3,
    "UGT1A1-related_disorder|not_provided|Crigler-Najjar_syndrome|Gilbert_syndrome|Lucey-Driscoll_syndrome|Hyperbilirubinemia": 1,
    "Crigler-Najjar_syndrome|_type_II|not_provided|UGT1A1-related_disorder": 1,
    "Lucey-Driscoll_syndrome|Gilbert_syndrome|not_provided|Crigler-Najjar_syndrome": 1,
    "Crigler-Najjar_syndrome_type_1|Crigler-Najjar_syndrome|_type_II|Lucey-Driscoll_syndrome|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_provided": 1,
    "UGT1A1-related_disorder|Crigler-Najjar_syndrome_type_1|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Gilbert_syndrome": 1,
    "BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Gilbert_syndrome": 1,
    "not_provided|Crigler-Najjar_syndrome_type_1": 1,
    "not_specified|UGT1A1-related_disorder|not_provided": 1,
    "Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|not_provided|UGT1A1-related_disorder": 1,
    "not_provided|Crigler-Najjar_syndrome|Gilbert_syndrome|Lucey-Driscoll_syndrome": 1,
    "Crigler-Najjar_syndrome|Hyperbilirubinemia|Lucey-Driscoll_syndrome|Gilbert_syndrome|not_provided": 1,
    "Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_provided|UGT1A1-related_disorder": 1,
    "Gilbert_syndrome|not_provided": 2,
    "UGT1A1-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|not_provided": 1,
    "BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|Crigler-Najjar_syndrome|_type_II|not_provided": 1,
    "not_provided|UGT1A1-related_disorder|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II": 1,
    "not_provided|Hyperbilirubinemia": 1,
    "not_provided|UGT1A9-related_disorder": 1,
    "UGT1A1-related_disorder|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|not_specified|not_provided|Hyperbilirubinemia": 1,
    "not_provided|Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome_type_1|UGT1A1-related_disorder": 1,
    "not_provided|Crigler-Najjar_syndrome|Lucey-Driscoll_syndrome|Gilbert_syndrome": 1,
    "Crigler-Najjar_syndrome|Crigler-Najjar_syndrome_type_1|not_provided": 1,
    "Crigler-Najjar_syndrome|not_specified": 1,
    "UGT1A1-related_disorder|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|Lucey-Driscoll_syndrome|not_provided": 1,
    "BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|not_provided": 1,
    "Gilbert_syndrome|Crigler-Najjar_syndrome|_type_II|not_specified": 1,
    "not_provided|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome": 1,
    "Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome_type_1|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome": 1,
    "not_provided|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "not_provided|Hyperbilirubinemia|UGT1A1-related_disorder": 1,
    "Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II": 1,
    "not_provided|UGT1A9-related_disorder|Crigler-Najjar_syndrome|Lucey-Driscoll_syndrome|Gilbert_syndrome": 1,
    "UGT1A1-related_disorder|Crigler-Najjar_syndrome_type_1|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome|_type_II|Lucey-Driscoll_syndrome|Gilbert_syndrome|not_provided|Crigler-Najjar_syndrome": 1,
    "UGT1A1-related_disorder|not_provided|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "not_provided|Crigler-Najjar_syndrome_type_1|Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II": 1,
    "Gilbert_syndrome|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Crigler-Najjar_syndrome_type_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II": 1,
    "not_provided|Lucey-Driscoll_syndrome|Gilbert_syndrome|Crigler-Najjar_syndrome": 1,
    "Lucey-Driscoll_syndrome|Gilbert_syndrome|Crigler-Najjar_syndrome|UGT1A1-related_disorder": 1,
    "UGT1A4-related_disorder": 1,
    "Crigler-Najjar_syndrome|not_specified|Lucey-Driscoll_syndrome|Gilbert_syndrome|not_provided": 1,
    "UGT1A1-related_disorder|BILIRUBIN|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome|_type_II|Gilbert_syndrome|Crigler-Najjar_syndrome_type_1|not_provided|Hyperbilirubinemia": 1,
    "Gilbert_syndrome|not_specified": 1,
    "Crigler-Najjar_syndrome|not_provided|Lucey-Driscoll_syndrome|Gilbert_syndrome|UGT1A1-related_disorder": 1,
    "Lucey-Driscoll_syndrome|Gilbert_syndrome|Crigler-Najjar_syndrome|not_provided": 1,
    "not_provided|Crigler-Najjar_syndrome|_type_II|Crigler-Najjar_syndrome": 1,
    "Gilbert_syndrome|Lucey-Driscoll_syndrome|Crigler-Najjar_syndrome": 1,
    "Crigler-Najjar_syndrome|Gilbert_syndrome|Lucey-Driscoll_syndrome": 2,
    "SPP2-related_disorder": 1,
    "not_provided|SPP2-related_disorder": 2,
    "SPP2-related_disorder|not_provided": 1,
    "Retinal_dystrophy|SPP2-related_disorder": 1,
    "Oculomotor-abducens_synkinesis|not_provided": 1,
    "Collagen_6-related_myopathy": 108,
    "Collagen_6-related_myopathy|not_provided": 12,
    "Collagen_6-related_myopathy|not_provided|not_specified": 2,
    "Bethlem_myopathy_1A": 3396,
    "COL6A3-related_disorder|Collagen_6-related_myopathy|not_specified|not_provided|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|not_provided": 487,
    "Bethlem_myopathy_1A|not_provided|COL6A3-related_disorder": 4,
    "not_provided|Bethlem_myopathy_1A|Myopathy": 1,
    "Bethlem_myopathy_1A|not_specified": 58,
    "COL6A3-related_disorder|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 5,
    "COL6A3-related_disorder": 19,
    "not_provided|Bethlem_myopathy_1A|Inborn_genetic_diseases": 31,
    "Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A": 48,
    "not_provided|Inborn_genetic_diseases|Bethlem_myopathy_1A": 28,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|not_specified": 9,
    "Inborn_genetic_diseases|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 12,
    "COL6A3-related_disorder|not_provided|Bethlem_myopathy_1A": 9,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 44,
    "Bethlem_myopathy_1A|COL6A3-related_disorder|not_provided": 4,
    "not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A": 77,
    "Bethlem_myopathy_1A|Inborn_genetic_diseases": 117,
    "COL6A3-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Dystonia_27": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified|not_provided": 8,
    "Bethlem_myopathy_1A|Inborn_genetic_diseases|not_provided": 30,
    "Dystonia_27|not_specified|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 2,
    "not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 14,
    "Ullrich_congenital_muscular_dystrophy_1A": 53,
    "COL6A3-related_disorder|not_specified|Dystonia_27|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "COL6A3-related_disorder|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 3,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided|not_specified": 14,
    "COL6A3-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Dystonia_27|Tip-toe_gait": 1,
    "Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|Bethlem_myopathy_1C|Inborn_genetic_diseases|Bethlem_myopathy_1A|not_provided": 1,
    "Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A|not_specified": 1,
    "Bethlem_myopathy_1A|Tip-toe_gait": 2,
    "COL6A3-related_disorder|Bethlem_myopathy_1A": 12,
    "not_specified|Dystonia_27|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy": 21,
    "COL6A3-related_disorder|Collagen_6-related_myopathy|not_specified|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|not_specified|not_provided|Bethlem_myopathy_1A": 2,
    "Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 16,
    "Dystonia_27|Bethlem_myopathy_1A|not_provided": 1,
    "Dystonia_27": 4,
    "not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 10,
    "not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 59,
    "COL6A3-related_disorder|not_specified|Bethlem_myopathy_1A": 2,
    "not_specified|Bethlem_myopathy_1A": 34,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided": 9,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|not_provided": 34,
    "Bethlem_myopathy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 3,
    "not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 9,
    "not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 3,
    "not_provided|Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|not_provided|Inborn_genetic_diseases": 27,
    "Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy|Dystonia_27": 1,
    "Dystonia_27|not_provided|Bethlem_myopathy_1A": 2,
    "Bethlem_myopathy_1C": 9,
    "not_provided|Bethlem_myopathy_1A|not_specified": 20,
    "COL6A3-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 7,
    "Bethlem_myopathy_1A|not_specified|not_provided": 22,
    "Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy|not_provided": 3,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided": 8,
    "Bethlem_myopathy": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A": 52,
    "not_provided|Bethlem_myopathy_1A|COL6A3-related_disorder": 6,
    "COL6A3-related_disorder|not_specified|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|See_cases|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Inborn_genetic_diseases|not_provided|Collagen_6-related_myopathy": 3,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Dystonia_27|not_specified|not_provided": 2,
    "not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Tip-toe_gait": 1,
    "not_provided|not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 3,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|not_provided": 5,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|Inborn_genetic_diseases": 2,
    "not_provided|Collagen_6-related_myopathy|Inborn_genetic_diseases|Dystonia_27|not_specified|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|See_cases": 2,
    "Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy": 4,
    "COL6A3-related_disorder|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|not_specified|not_provided": 1,
    "Collagen_6-related_myopathy|Dystonia_27|not_specified|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "COL6A3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Bethlem_myopathy_1A|not_provided": 15,
    "Bethlem_myopathy_1A|COL6A3-related_disorder": 16,
    "Inborn_genetic_diseases|Dystonia_27|not_provided|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|not_specified|not_provided|Bethlem_myopathy_1A": 2,
    "not_specified|not_provided|Bethlem_myopathy_1A": 37,
    "COL6A3-related_disorder|Dystonia_27|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1C|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Dystonia_27|Bethlem_myopathy_1A|not_provided": 1,
    "COL6A3-related_disorder|not_specified|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|Collagen_6-related_myopathy": 1,
    "not_provided|COL6A3-related_disorder|Bethlem_myopathy_1A": 5,
    "COL6A3-related_disorder|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 13,
    "Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|not_provided|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|Dystonia_27": 1,
    "COL6A3-related_disorder|Bethlem_myopathy_1C|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27": 1,
    "not_provided|not_specified|Bethlem_myopathy_1A": 19,
    "COL6A3-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Bethlem_myopathy_1A": 1,
    "not_specified|COL6A3-related_disorder|not_provided|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 15,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Tip-toe_gait": 1,
    "COL6A3-related_disorder|not_provided": 3,
    "not_provided|Limb-girdle_muscular_dystrophy|Bethlem_myopathy_1A": 2,
    "Bethlem_myopathy_1C|Bethlem_myopathy_1A": 1,
    "Dystonia_27|not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "Dystonia_27|Bethlem_myopathy_1A": 4,
    "Bethlem_myopathy_1A|Muscle_weakness": 1,
    "COL6A3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1C": 1,
    "not_provided|COL6A3-related_disorder": 1,
    "Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A|Inborn_genetic_diseases": 1,
    "Bethlem_myopathy_1A|Dystonia_27|Collagen_6-related_myopathy|not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "COL6A3-related_disorder|Bethlem_myopathy_1A|not_provided": 1,
    "Inborn_genetic_diseases|Collagen_6-related_myopathy": 2,
    "Bethlem_myopathy_1A|not_provided|not_specified": 7,
    "Inborn_genetic_diseases|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 4,
    "Bethlem_myopathy_1A|not_specified|Ullrich_congenital_muscular_dystrophy_1A|Dystonia_27|not_provided": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|Bethlem_myopathy_1C|not_provided": 1,
    "not_provided|Bethlem_myopathy_1A|Tip-toe_gait": 2,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_provided": 7,
    "Bethlem_myopathy_1A|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|not_specified|Collagen_6-related_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|not_provided|Bethlem_myopathy_1A": 4,
    "not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 7,
    "COL6A3-related_phenotype": 1,
    "Bethlem_myopathy_1A|Dystonia_27": 3,
    "Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "Limb-girdle_muscular_dystrophy|Myopathy|not_provided": 1,
    "Bethlem_myopathy_1A|not_specified|not_provided|COL6A3-related_disorder": 1,
    "Myopathy|Inborn_genetic_diseases|Bethlem_myopathy_1A": 1,
    "not_specified|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 2,
    "Bethlem_myopathy_1A|not_specified|Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|COL6A3-related_disorder": 1,
    "not_provided|Dystonia_27|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|not_provided|Bethlem_myopathy_1A|not_specified": 1,
    "COL6A3-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Congenital_contracture": 1,
    "COL6A3-related_disorder|Muscular_dystrophy|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Dystonia_27|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|not_provided|Collagen_6-related_myopathy|Dystonia_27|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|not_provided": 1,
    "not_specified|Bethlem_myopathy_1A|Inborn_genetic_diseases|not_provided": 1,
    "COL6A3-related_disorder|Dystonia_27|not_provided|Bethlem_myopathy_1A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|COL6A3-related_disorder|not_provided": 1,
    "not_provided|Bethlem_myopathy_1A|Inborn_genetic_diseases|Dystonia_27": 1,
    "COL6A3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Tip-toe_gait": 1,
    "Bethlem_myopathy_1A|COL6A3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Bethlem_myopathy_1A|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 3,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|Inborn_genetic_diseases": 2,
    "Bethlem_myopathy_1A|not_provided|Tip-toe_gait": 1,
    "Bethlem_myopathy_1A|COL6A3-related_disorder|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "Bethlem_myopathy_1A|not_provided|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Bethlem_myopathy_1A": 2,
    "Collagen_6-related_myopathy|Inborn_genetic_diseases": 2,
    "Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy|not_specified": 4,
    "not_provided|Collagen_6-related_myopathy": 5,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|not_specified|not_provided|Collagen_6-related_myopathy": 3,
    "Bethlem_myopathy_1C|not_provided|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|not_specified|Bethlem_myopathy_1A": 2,
    "COL6A3-related_disorder|not_specified|Dystonia_27|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|Dystonia_27|not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Bethlem_myopathy_1A": 4,
    "Bethlem_myopathy_1C|COL6A3-related_disorder": 1,
    "Dystonia_27|COL6A3-related_disorder|not_provided|Bethlem_myopathy_1A": 1,
    "Dystonia_27|Bethlem_myopathy_1A|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Dystonia_27|not_specified|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|Dystonia_27|not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Inborn_genetic_diseases|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_provided": 1,
    "COL6A3-related_disorder|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy|COL6A3-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Bethlem_myopathy_1A|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|COL6A3-related_disorder|not_provided": 1,
    "not_provided|Collagen_6-related_myopathy|not_specified|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Tip-toe_gait": 1,
    "Dystonia_27|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1A|not_specified|Inborn_genetic_diseases": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|COL6A3-related_disorder": 1,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Dystonia_27": 1,
    "not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Collagen_6-related_myopathy": 1,
    "Dystonia_27|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 11,
    "Collagen_6-related_myopathy|not_specified|Bethlem_myopathy_1A|not_provided": 4,
    "Bethlem_myopathy_1A|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 2,
    "Collagen_6-related_myopathy|Inborn_genetic_diseases|not_provided|COL6A3-related_disorder|Bethlem_myopathy_1A|not_specified": 1,
    "not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified|not_provided|COL6A3-related_disorder": 1,
    "Bethlem_myopathy_1A|Inborn_genetic_diseases|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|not_provided|Collagen_6-related_myopathy": 1,
    "not_specified|not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Inborn_genetic_diseases|Dystonia_27": 1,
    "Collagen_6-related_myopathy|Inborn_genetic_diseases|not_specified|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|Dystonia_27|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 2,
    "not_provided|Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Dystonia_27|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "not_provided|Collagen_6-related_myopathy|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Dystonia_27|not_provided|not_specified": 1,
    "Muscle_tissue_disorder": 5,
    "COL6A3-related_disorder|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Dystonia_27|not_provided": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|not_provided|COL6A3-related_disorder": 1,
    "Bethlem_myopathy_1A|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "COL6A3-related_disorder|not_specified|Bethlem_myopathy_1A|not_provided": 1,
    "Inborn_genetic_diseases|Tip-toe_gait|not_provided|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|Dystonia_27|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|COL6A3-related_disorder": 1,
    "not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Inborn_genetic_diseases": 1,
    "not_specified|COL6A3-related_disorder|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|Inborn_genetic_diseases|Bethlem_myopathy_1A|not_specified|not_provided": 1,
    "Bethlem_myopathy_1A|Bethlem_myopathy_1C": 1,
    "not_provided|not_specified|Bethlem_myopathy_1A|Intellectual_disability": 1,
    "COL6A3-related_disorder|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_provided": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|not_specified": 1,
    "not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Tip-toe_gait": 1,
    "not_specified|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 3,
    "Ullrich_congenital_muscular_dystrophy_1A|Dystonia_27|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1C|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|not_provided|not_specified|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified": 1,
    "Limb-girdle_muscular_dystrophy|Bethlem_myopathy_1A|not_provided": 1,
    "not_provided|Bethlem_myopathy_1A|Inborn_genetic_diseases|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1C|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1C": 1,
    "not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided": 3,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1C|COL6A3-related_disorder": 1,
    "Bethlem_myopathy_1A|not_specified|COL6A3-related_disorder|Collagen_6-related_myopathy|not_provided": 1,
    "not_provided|Bethlem_myopathy_1A|Dystonia_27": 1,
    "Dystonia_27|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "COL6A3-related_disorder|not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_specified|Bethlem_myopathy_1A|not_provided|Tip-toe_gait|COL6A3-related_disorder": 1,
    "not_provided|Bethlem_myopathy_1C|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1C|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|not_specified|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Dystonia_27": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1C": 1,
    "not_provided|Inborn_genetic_diseases|Bethlem_myopathy_1A|COL6A3-related_disorder": 1,
    "not_provided|Dystonia_27": 1,
    "Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "COL6A3-related_disorder|Dystonia_27|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "COL6A3-related_phenotype|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_provided|not_specified|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|Dystonia_27|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 2,
    "not_specified|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1A|Multiple_joint_contractures": 1,
    "Bethlem_myopathy_1A|Spinocerebellar_ataxia_type_13": 1,
    "Bethlem_myopathy_1A|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A|Collagen_6-related_myopathy|not_specified": 1,
    "Bethlem_myopathy_1A|Dystonia_27|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "COL6A3-related_disorder|Collagen_6-related_myopathy|Inborn_genetic_diseases|not_specified|Bethlem_myopathy_1A|not_provided": 1,
    "Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|Bethlem_myopathy_1A": 1,
    "COL6A3-related_disorder|Bethlem_myopathy_1A|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Bethlem_myopathy_1C|Ullrich_congenital_muscular_dystrophy_1C|Dystonia_27|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Inborn_genetic_diseases": 1,
    "not_provided|Dystonia_27|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_provided|MLPH-related_disorder": 5,
    "not_provided|Griscelli_syndrome_type_3": 5,
    "Griscelli_syndrome_type_3": 8,
    "MLPH-related_disorder|not_provided": 6,
    "MLPH-related_disorder": 3,
    "not_provided|Griscelli_syndrome_type_3|MLPH-related_disorder": 1,
    "Inborn_genetic_diseases|MLPH-related_disorder": 1,
    "not_specified|not_provided|MLPH-related_disorder": 1,
    "Griscelli_syndrome_type_3|not_provided": 1,
    "not_provided|MLPH-related_disorder|not_specified": 1,
    "not_provided|not_specified|MLPH-related_disorder": 1,
    "Inborn_genetic_diseases|Griscelli_syndrome_type_3|MLPH-related_disorder": 1,
    "not_specified|not_provided|MLPH-related_disorder|Inborn_genetic_diseases": 1,
    "PER2-related_disorder": 20,
    "Advanced_sleep_phase_syndrome_1": 9,
    "not_provided|PER2-related_disorder": 3,
    "PER2-related_disorder|not_provided": 2,
    "Advanced_sleep_phase_syndrome_1|not_specified": 1,
    "not_specified|Advanced_sleep_phase_syndrome_1": 1,
    "not_specified|PER2-related_disorder": 1,
    "Senior-Loken_syndrome_9": 8,
    "not_provided|Senior-Loken_syndrome_9": 6,
    "Senior-Loken_syndrome_9|not_provided": 3,
    "not_provided|TRAF3IP1-related_disorder|Inborn_genetic_diseases": 1,
    "TRAF3IP1-related_disorder|not_provided": 2,
    "not_provided|TRAF3IP1-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Senior-Loken_syndrome_9": 1,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|TRAF3IP1-related_disorder": 1,
    "not_provided|Senior-Loken_syndrome_9|Inborn_genetic_diseases": 1,
    "Ellis-van_Creveld_syndrome": 399,
    "Jeune_thoracic_dystrophy|not_provided|Senior-Loken_syndrome_9": 1,
    "Senior-Loken_syndrome_9|Inborn_genetic_diseases|not_provided": 1,
    "TWIST2-related_disorder": 2,
    "not_provided|TWIST2-related_disorder": 1,
    "Focal_facial_dermal_dysplasia_type_III": 2,
    "Ablepharon_macrostomia_syndrome|Inborn_genetic_diseases": 1,
    "Barber-Say_syndrome": 3,
    "Focal_facial_dermal_dysplasia_type_III|not_provided": 1,
    "HDAC4-related_disorder": 27,
    "HDAC4-related_disorder|not_provided": 5,
    "Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 28,
    "not_provided|HDAC4-related_disorder": 9,
    "Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|Chromosome_2q37_deletion_syndrome": 1,
    "not_provided|Chromosome_2q37_deletion_syndrome": 2,
    "HDAC4-related_disorder|not_specified|not_provided|Chromosome_2q37_deletion_syndrome": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|HDAC4-related_disorder": 1,
    "Intellectual_disability|not_provided|HDAC4-related_disorder": 1,
    "not_provided|not_specified|Chromosome_2q37_deletion_syndrome": 2,
    "Chromosome_2q37_deletion_syndrome|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|not_provided": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 2,
    "Inborn_genetic_diseases|not_provided|Chromosome_2q37_deletion_syndrome|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 1,
    "Inborn_genetic_diseases|HDAC4-related_disorder|not_provided": 1,
    "not_provided|Chromosome_2q37_deletion_syndrome|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 1,
    "Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|Chromosome_2q37_deletion_syndrome": 1,
    "Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|not_provided": 1,
    "HDAC4-related_disorder|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|VATER_association": 1,
    "not_provided|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|Brachydactyly_syndrome_type_E|not_provided|Chromosome_2q37_deletion_syndrome|Intellectual_disability|_profound": 1,
    "HDAC4-related_disorder|Intellectual_disability|_severe|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 1,
    "Chromosome_2q37_deletion_syndrome": 2,
    "Inborn_genetic_diseases|HDAC4-related_disorder": 2,
    "Chromosome_2q37_deletion_syndrome|not_provided": 1,
    "Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies|not_provided|Inborn_genetic_diseases|Chromosome_2q37_deletion_syndrome|Intellectual_disability|not_specified": 1,
    "HDAC4-related_disorder|Neurodevelopmental_disorder_with_central_hypotonia_and_dysmorphic_facies": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_22": 10,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_22|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "NDUFA10-related_disorder|not_specified|not_provided": 1,
    "NDUFA10-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_22": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_22|NDUFA10-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_22|not_provided": 1,
    "NDUFA10-related_disorder|not_provided": 1,
    "not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_22": 2,
    "not_provided|NDUFA10-related_disorder": 2,
    "not_provided|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_22|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_22|Leigh_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified": 4,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_22": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFA10-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_22|not_provided|Leigh_syndrome": 1,
    "Leigh_syndrome|NDUFA10-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_22|Inborn_genetic_diseases": 1,
    "NDUFA10-related_disorder|not_provided|not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "NDUFA10-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_22|Leigh_syndrome": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFA10-related_disorder|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|Leigh_syndrome|not_provided": 3,
    "not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 2,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|not_provided": 3,
    "GPC1-related_disorder": 2,
    "CAPN10-related_disorder": 12,
    ".|Type_2_diabetes_mellitus_1|_susceptibility_to": 1,
    "Type_2_diabetes_mellitus_1|_susceptibility_to": 3,
    "CAPN10-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|CAPN10-related_disorder": 1,
    "not_provided|CAPN10-related_disorder": 2,
    "Diabetes_mellitus|_noninsulin-dependent|_1": 1,
    "Hereditary_spastic_paraplegia_30|not_provided": 16,
    "Hereditary_spastic_paraplegia_30": 116,
    "not_provided|Hereditary_spastic_paraplegia_30": 6,
    "Spastic_Paraplegia|_Recessive|Intellectual_Disability|_Dominant|Hereditary_sensory_and_autonomic_neuropathy_type_2": 2,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 47,
    "KIF1A-related_disorder": 21,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1301,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C": 3,
    "not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 28,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 118,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Inborn_genetic_diseases": 14,
    "KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 2,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 165,
    "not_specified|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 2,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 135,
    "Hereditary_spastic_paraplegia|KIF1A-related_disorder|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 2,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 4,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 22,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases": 10,
    "KIF1A-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 18,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 26,
    "Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C": 6,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|not_specified": 4,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified": 10,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 16,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 10,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided|Hereditary_spastic_paraplegia": 3,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 4,
    "Hereditary_spastic_paraplegia_30|not_provided|History_of_neurodevelopmental_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 9,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_provided": 9,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 60,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|History_of_neurodevelopmental_disorder|not_provided": 2,
    "KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_provided": 2,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 3,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 2,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|not_provided": 4,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_provided": 13,
    "Hereditary_spastic_paraplegia|not_specified|KIF1A-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_2|not_provided|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|Spastic_Paraplegia|_Recessive|Intellectual_Disability|_Dominant|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|not_provided": 22,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "not_specified|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 5,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|not_specified": 2,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 9,
    "not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 10,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 30,
    "Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 2,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|KIF1A-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|not_specified|KIF1A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases": 6,
    "Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_ataxia|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Intellectual_disability": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 2,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|not_specified|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Hereditary_spastic_paraplegia": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided": 3,
    "Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_provided|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_specified": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided|KIF1A-related_disorder": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 6,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|KIF1A-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 2,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified": 5,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 15,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases": 10,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Intellectual_disability": 1,
    "Hereditary_spastic_paraplegia|KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|KIF1A-related_disorder": 1,
    "KIF1A-related_disorder|History_of_neurodevelopmental_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 4,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 2,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_specified|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|See_cases": 1,
    "KIF1A-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_specified|Inborn_genetic_diseases": 5,
    "Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 7,
    "Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "KIF1A_related_neurological_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 9,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided": 5,
    "not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia|not_specified": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 9,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 4,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9": 3,
    "not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|not_provided": 3,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder": 4,
    "not_provided|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder": 4,
    "KIF1A-related_disorder|not_provided|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided|Inborn_genetic_diseases": 3,
    "KIF1A-related_disorder|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 3,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 4,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_specified": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|_autosomal_dominant|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases|KIF1A-related_disorder": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_sensory_and_autonomic_neuropathy_type_2|not_specified|Intellectual_disability|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Spastic_Paraplegia|_Recessive|Intellectual_Disability|_Dominant|Inborn_genetic_diseases": 1,
    "KIF1A-related_disorder|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder": 3,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_specified": 3,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|History_of_neurodevelopmental_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 2,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|not_specified|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "Inborn_genetic_diseases|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "History_of_neurodevelopmental_disorder|Hereditary_spastic_paraplegia_30|Spastic_paraplegia_30b|_autosomal_recessive|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|History_of_neurodevelopmental_disorder": 1,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified": 2,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_specified": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|KIF1A-related_disorder": 1,
    "KIF1A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|not_provided|not_specified|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "History_of_neurodevelopmental_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_specified|not_provided|Hereditary_spastic_paraplegia": 4,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia|not_specified": 1,
    "KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder": 1,
    "KIF1A-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 2,
    "Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 2,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 2,
    "Hereditary_ataxia|KIF1A-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|not_specified|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "not_specified|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "not_provided|KIF1A-related_disorder|Inborn_genetic_diseases|not_specified|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "Intellectual_disability|_autosomal_dominant_9|not_provided": 4,
    "Intellectual_disability|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Inborn_genetic_diseases|not_provided": 1,
    "KIF1A_related_neurological_disorder|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "Inborn_genetic_diseases|KIF1A-related_disorder|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Spastic_paraplegia_30b|_autosomal_recessive": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided|Inborn_genetic_diseases": 4,
    "KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory|_type_2C": 3,
    "not_provided|KIF1A-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_provided|KIF1A_related_neurological_disorder|KIF1A-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30": 1,
    "not_specified|KIF1A_related_neurological_disorder|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_9": 1,
    "KIF1A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|KIF1A_related_neurological_disorder": 1,
    "KIF1A-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_specified|Hereditary_spastic_paraplegia|KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Hereditary_spastic_paraplegia_30|KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_provided": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided|not_specified": 2,
    "KIF1A-related_disorder|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "KIF1A-related_disorder|Intellectual_disability|_autosomal_dominant_9|Intellectual_disability|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_specified|not_provided": 3,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|KIF1A-related_disorder|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|KIF1A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder": 1,
    "not_provided|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_specified|not_provided": 2,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "not_specified|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 2,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|KIF1A-related_disorder": 1,
    "KIF1A-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder": 1,
    "Hereditary_spastic_paraplegia_30|not_specified|History_of_neurodevelopmental_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|not_provided|not_specified|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "KIF1A-related_disorder|not_provided": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided|Hereditary_spastic_paraplegia": 2,
    "KIF1A-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|KIF1A-related_disorder": 1,
    "not_provided|KIF1A-related_disorder": 2,
    "Spastic_ataxia|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30": 2,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided|KIF1A-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Spastic_paraplegia_30b|_autosomal_recessive": 1,
    "not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Charcot-Marie-Tooth_disease_type_2|Spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|KIF1A-related_disorder": 1,
    "Hereditary_spastic_paraplegia|KIF1A_related_neurological_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Inborn_genetic_diseases|KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Spastic_paraplegia": 1,
    "not_provided|not_specified|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Craniosynostosis_syndrome": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|not_provided|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Spastic_paraplegia_30b|_autosomal_recessive": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "Spastic_paraplegia_30b|_autosomal_recessive": 1,
    "KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided": 1,
    "KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases": 1,
    "KIF1A-related_disorder|PEHO_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_9": 1,
    "Hereditary_spastic_paraplegia_30|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Inborn_genetic_diseases|PEHO_syndrome|Syndromic_intellectual_disability": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Intellectual_disability|_autosomal_dominant_9": 1,
    "Intellectual_disability|_autosomal_dominant_9|not_provided|Autosomal_dominant_non-syndromic_intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_9|not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|KIF1A-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_2C|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases": 1,
    "KIF1A-related_disorder|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|History_of_neurodevelopmental_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_30|not_specified": 2,
    "KIF1A-related_disorder|PEHO_syndrome|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|not_specified|Hereditary_spastic_paraplegia": 1,
    "KIF1A-related_disorder|Hereditary_spastic_paraplegia_30": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hyperreflexia|Lower_limb_hyperreflexia|Clonus|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "KIF1A-related_disorder|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_30|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "not_specified|Inborn_genetic_diseases|KIF1A-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9": 1,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia": 1,
    "Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Inborn_genetic_diseases|not_provided|Neurodevelopmental_delay": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Spastic_Paraplegia|_Recessive|Intellectual_Disability|_Dominant|Hereditary_sensory_and_autonomic_neuropathy_type_2|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|Neuropathy|_hereditary_sensory|_type_2C|not_provided": 1,
    "Intellectual_disability|not_provided|Hereditary_spastic_paraplegia": 1,
    "Intellectual_disability|_autosomal_dominant_9|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|not_provided|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|Intellectual_disability|_autosomal_dominant_9|See_cases|KIF1A_related_neurological_disorder|Neuropathy|_hereditary_sensory|_type_2C": 1,
    "not_provided|Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|Spastic_paraplegia_30b|_autosomal_recessive": 1,
    "Hereditary_spastic_paraplegia_30|Neuropathy|_hereditary_sensory|_type_2C|Intellectual_disability|_autosomal_dominant_9|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_30": 1,
    "not_provided|Primary_hyperoxaluria": 3,
    "Primary_hyperoxaluria|_type_I": 293,
    "not_provided|Primary_hyperoxaluria|_type_I": 109,
    "AGXT-related_disorder": 3,
    "Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 20,
    "not_specified|Primary_hyperoxaluria|_type_I": 5,
    "Alanine_glyoxylate_aminotransferase_deficiency|AGXT-related_disorder|Inborn_genetic_diseases|Nephrotic_syndrome|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "AGXT-related_disorder|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 2,
    "not_provided|not_specified|Primary_hyperoxaluria|_type_I": 3,
    "Alanine_glyoxylate_aminotransferase_deficiency|not_provided": 1,
    "AGXT-related_disorder|Alanine_glyoxylate_aminotransferase_deficiency|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "Inborn_genetic_diseases|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 2,
    "not_specified|not_provided|Primary_hyperoxaluria|_type_I": 18,
    "Inborn_genetic_diseases|not_provided|Primary_hyperoxaluria|_type_I": 3,
    "Hyperoxaluria": 5,
    "Primary_hyperoxaluria|_type_I|not_provided": 37,
    "Nephrocalcinosis|Nephrolithiasis|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 2,
    "not_provided|Primary_hyperoxaluria|_type_I|not_specified": 1,
    "Primary_hyperoxaluria": 9,
    "Primary_hyperoxaluria|Primary_hyperoxaluria|_type_I": 6,
    "Primary_hyperoxaluria|_type_I|Primary_hyperoxaluria": 1,
    "AGXT-related_disorder|not_provided|Primary_hyperoxaluria|_type_I": 3,
    "not_provided|Primary_hyperoxaluria|_type_I|Abnormality_of_metabolism/homeostasis": 1,
    "Primary_hyperoxaluria|_type_I|See_cases": 1,
    "Primary_hyperoxaluria|Hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "AGXT-related_disorder|not_specified": 1,
    "not_provided|AGXT-related_disorder": 1,
    "Primary_hyperoxaluria|_type_I|not_specified": 1,
    "Primary_hyperoxaluria|_type_I|AGXT-related_disorder|not_provided": 2,
    "not_provided|Primary_hyperoxaluria|_type_I|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Primary_hyperoxaluria|_type_I|Inborn_genetic_diseases": 3,
    "Alanine_glyoxylate_aminotransferase_deficiency|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "AGXT-related_disorder|Primary_hyperoxaluria|_type_I|not_provided": 1,
    "Nephrocalcinosis|Nephrolithiasis|AGXT-related_disorder|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "Primary_hyperoxaluria|_type_I|not_specified|not_provided": 1,
    "not_provided|AGXT-related_disorder|Primary_hyperoxaluria|_type_I": 1,
    "Cardiac_arrhythmia|Primary_hyperoxaluria|Primary_hyperoxaluria|_type_I": 1,
    "AGXT-related_disorder|not_specified|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "Inborn_genetic_diseases|Primary_hyperoxaluria|_type_I": 1,
    "Alanine_glyoxylate_aminotransferase_deficiency|not_specified|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "Inborn_genetic_diseases|Primary_hyperoxaluria|_type_I|AGXT-related_disorder|not_provided": 1,
    "not_provided|Primary_hyperoxaluria|_type_I|AGXT-related_disorder": 1,
    "Nephrocalcinosis|Nephrolithiasis": 1,
    "not_provided|Primary_hyperoxaluria|_type_I|Primary_hyperoxaluria": 1,
    "Alanine_glyoxylate_aminotransferase_deficiency|not_provided|Primary_hyperoxaluria|_type_I": 1,
    "PASK-related_disorder": 6,
    "PASK-related_disorder|not_provided": 1,
    "PASK-related_disorder|not_specified|not_provided": 1,
    "PASK-related_disorder|not_specified": 1,
    "HDLBP-related_disorder": 22,
    "HDLBP-related_disorder|not_provided": 8,
    "not_provided|HDLBP-related_disorder": 4,
    "Fine-Lubinsky_syndrome": 3,
    "Neurodegeneration|_childhood-onset|_with_progressive_microcephaly": 6,
    "D-2-hydroxyglutaric_aciduria_1": 230,
    "D-2-hydroxyglutaric_aciduria_1|not_provided": 16,
    "D-2-hydroxyglutaric_aciduria_1|not_specified": 6,
    "D-2-hydroxyglutaric_aciduria_1|Inborn_genetic_diseases": 13,
    "D-2-hydroxyglutaric_aciduria_1|not_specified|not_provided": 5,
    "not_provided|D-2-hydroxyglutaric_aciduria_1|D2HGDH-related_disorder|Inborn_genetic_diseases": 1,
    "D-2-hydroxyglutaric_aciduria_1|not_provided|not_specified": 2,
    "not_provided|D-2-hydroxyglutaric_aciduria_1": 7,
    "Inborn_genetic_diseases|D-2-hydroxyglutaric_aciduria_1": 6,
    "Inborn_genetic_diseases|not_specified|D-2-hydroxyglutaric_aciduria_1": 1,
    "not_specified|D-2-hydroxyglutaric_aciduria_1|not_provided": 2,
    "not_specified|not_provided|D-2-hydroxyglutaric_aciduria_1": 3,
    "D2HGDH-related_disorder|not_specified|not_provided|D-2-hydroxyglutaric_aciduria_1": 2,
    "not_specified|D-2-hydroxyglutaric_aciduria_1": 6,
    "D-2-hydroxyglutaric_aciduria_1|D2HGDH-related_disorder": 6,
    "Inborn_genetic_diseases|not_provided|D-2-hydroxyglutaric_aciduria_1": 1,
    "D-2-hydroxyglutaric_aciduria_1|not_specified|D-2-hydroxyglutaric_aciduria": 1,
    "D-2-hydroxyglutaric_aciduria_1|not_provided|D-2-hydroxyglutaric_aciduria|not_specified": 1,
    "D-2-hydroxyglutaric_aciduria_1|not_provided|D2HGDH-related_disorder": 1,
    "D-2-hydroxyglutaric_aciduria_1|not_provided|Inborn_genetic_diseases": 2,
    "D-2-hydroxyglutaric_aciduria_1|D2HGDH-related_disorder|not_specified": 3,
    "not_provided|D-2-hydroxyglutaric_aciduria_1|not_specified": 2,
    "D-2-hydroxyglutaric_aciduria_1|not_specified|not_provided|D2HGDH-related_disorder": 1,
    "D2HGDH-related_disorder": 1,
    "D-2-hydroxyglutaric_aciduria": 3,
    "not_provided|not_specified|D-2-hydroxyglutaric_aciduria_1": 2,
    "D2HGDH-related_disorder|D-2-hydroxyglutaric_aciduria_1": 4,
    "not_specified|D2HGDH-related_disorder|D-2-hydroxyglutaric_aciduria_1": 1,
    "D2HGDH-related_disorder|not_specified|D-2-hydroxyglutaric_aciduria_1|not_provided": 1,
    "D2HGDH-related_disorder|not_provided|D-2-hydroxyglutaric_aciduria_1": 1,
    "not_provided|D-2-hydroxyglutaric_aciduria_1|Inborn_genetic_diseases": 3,
    "not_specified|D-2-hydroxyglutaric_aciduria_1|D2HGDH-related_disorder": 1,
    "D2HGDH-related_disorder|not_specified|D-2-hydroxyglutaric_aciduria_1": 1,
    "D-2-hydroxyglutaric_aciduria_1|not_specified|D2HGDH-related_disorder|not_provided": 1,
    "D-2-hydroxyglutaric_aciduria_1|D2HGDH-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "D-2-hydroxyglutaric_aciduria_1|Inborn_genetic_diseases|not_specified": 1,
    "PDCD1-related_disorder|not_provided": 1,
    "not_provided|PDCD1-related_disorder|not_specified": 1,
    "RECLASSIFIED_-_PDCD1_POLYMORPHISM": 1,
    "PDCD1-related_disorder": 3,
    "CHL1-related_disorder|not_provided": 9,
    "CHL1-related_disorder": 9,
    "not_provided|CHL1-related_disorder": 6,
    "CHL1-related_disorder|not_specified": 1,
    "not_provided|CHL1-related_disorder|not_specified": 1,
    "CNTN6-related_disorder": 17,
    "CNTN6-related_disorder|not_provided": 4,
    "not_specified|CNTN6-related_disorder": 1,
    "not_provided|CNTN6-related_disorder": 6,
    "CNTN4-associated_neurodevelopmental_disorder": 1,
    "CNTN4-related_disorder": 6,
    "Lip_and_oral_cavity_carcinoma": 17,
    "not_provided|CNTN4-related_disorder": 6,
    "CNTN4-related_disorder|not_provided": 5,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 414,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Inborn_genetic_diseases": 10,
    "not_specified|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 4,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinal_dystrophy": 4,
    "TRNT1-related_disorder|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 3,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinal_dystrophy|not_specified": 1,
    "not_provided|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis|not_specified": 1,
    "Optic_atrophy|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 18,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_specified|not_provided": 2,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis|not_provided|not_specified": 1,
    "TRNT1-related_disorder": 2,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_and_erythrocytic_microcytosis|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 1,
    "not_provided|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 6,
    "not_specified|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa_and_erythrocytic_microcytosis|not_provided": 1,
    "not_specified|Retinal_dystrophy|not_provided|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided|Retinal_dystrophy": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided": 8,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_specified": 2,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_specified|TRNT1-related_disorder": 1,
    "Retinitis_pigmentosa_and_erythrocytic_microcytosis|not_provided|TRNT1-related_disorder|Retinal_dystrophy|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided|TRNT1-related_disorder": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinal_dystrophy|TRNT1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 1,
    "Inborn_genetic_diseases|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 7,
    "Inborn_genetic_diseases|not_provided|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 1,
    "TRNT1-related_disorder|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided": 1,
    "Retinal_dystrophy|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided|not_specified|Retinal_dystrophy": 1,
    "not_provided|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|TRNT1-related_disorder|Retinitis_pigmentosa_and_erythrocytic_microcytosis": 1,
    "not_provided|Retinitis_pigmentosa_and_erythrocytic_microcytosis|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis|not_provided": 1,
    "not_specified|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_and_erythrocytic_microcytosis|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_specified|Retinal_dystrophy": 1,
    "not_specified|Retinitis_pigmentosa_and_erythrocytic_microcytosis|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Retinitis_pigmentosa_and_erythrocytic_microcytosis|TRNT1-related_disorder|not_provided": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|Developmental_and_epileptic_encephalopathy|_57": 1,
    "Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|TRNT1-related_disorder|Retinitis_pigmentosa_and_erythrocytic_microcytosis|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_sideroblastic_anemia-B-cell_immunodeficiency-periodic_fever-developmental_delay_syndrome|not_provided|Retinal_dystrophy": 1,
    "CRBN-related_disorder|not_specified": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_2": 3,
    "not_provided|CRBN-related_disorder": 2,
    "CRBN-related_disorder": 3,
    "Intellectual_disability|_autosomal_recessive_2": 5,
    "not_provided|Intellectual_disability|not_specified": 5,
    "Intellectual_disability|_autosomal_recessive_2|not_provided": 2,
    "Intellectual_disability|_autosomal_recessive_2|not_specified|not_provided": 1,
    "not_provided|CRBN-related_disorder|Intellectual_disability|_autosomal_recessive_2": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_2|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_2|Inborn_genetic_diseases": 1,
    "Multiple_sulfatase_deficiency": 627,
    "not_provided|Multiple_sulfatase_deficiency": 23,
    "Multiple_sulfatase_deficiency|not_provided": 14,
    "Multiple_sulfatase_deficiency|not_specified|not_provided": 3,
    "Multiple_sulfatase_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Multiple_sulfatase_deficiency": 10,
    "Multiple_sulfatase_deficiency|Inborn_genetic_diseases": 19,
    "Multiple_sulfatase_deficiency|SUMF1-related_disorder|not_provided": 1,
    "Multiple_sulfatase_deficiency|Spinocerebellar_ataxia_type_15/16": 1,
    "Multiple_sulfatase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "SUMF1-related_disorder|Multiple_sulfatase_deficiency": 4,
    "not_provided|Multiple_sulfatase_deficiency|Inborn_genetic_diseases": 2,
    "not_specified|Multiple_sulfatase_deficiency": 3,
    "not_specified|not_provided|Multiple_sulfatase_deficiency": 3,
    "Multiple_sulfatase_deficiency|SUMF1-related_disorder": 2,
    "SUMF1-related_disorder|Multiple_sulfatase_deficiency|not_provided": 1,
    "Multiple_sulfatase_deficiency|not_specified": 1,
    "SUMF1-related_disorder": 2,
    "See_cases|Multiple_sulfatase_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Multiple_sulfatase_deficiency|not_provided": 1,
    "SUMF1-related_disorder|not_provided|Multiple_sulfatase_deficiency": 1,
    "not_provided|Multiple_sulfatase_deficiency|not_specified": 2,
    "not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia": 11,
    "Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16|not_specified|Autosomal_dominant_cerebellar_ataxia|not_provided": 3,
    "not_provided|not_specified|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_29|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_29": 1,
    "ITPR1-related_disorder": 11,
    "not_provided|Autosomal_dominant_cerebellar_ataxia": 43,
    "not_specified|not_provided|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 2,
    "Gillespie_syndrome": 25,
    "not_provided|Spinocerebellar_ataxia_type_15/16|Autosomal_dominant_cerebellar_ataxia": 1,
    "Spinocerebellar_ataxia_type_29": 26,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|not_specified": 8,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|not_provided": 12,
    "ITPR1-related_disorder|Gillespie_syndrome": 1,
    "not_provided|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases": 4,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|not_provided|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_29|not_provided|Spinocerebellar_ataxia_type_15/16": 1,
    "not_provided|Spinocerebellar_ataxia_type_15/16": 5,
    "ITPR1-related_disorder|not_provided": 13,
    "Spinocerebellar_ataxia_type_15/16": 16,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|not_specified": 4,
    "not_provided|Spinocerebellar_ataxia_type_29": 4,
    "Spinocerebellar_ataxia_type_29|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_15/16|not_provided": 1,
    "Inborn_genetic_diseases|Gillespie_syndrome|Neurodevelopmental_disorder|Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|not_provided": 1,
    "Gillespie_syndrome|not_provided": 2,
    "not_provided|ITPR1-related_disorder|not_specified|Autosomal_dominant_cerebellar_ataxia": 2,
    "Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome|not_provided": 2,
    "Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29": 1,
    "Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome": 1,
    "not_specified|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16|Autosomal_dominant_cerebellar_ataxia|not_provided": 2,
    "not_specified|not_provided|ITPR1-related_disorder": 4,
    "Spinocerebellar_ataxia_type_29|not_provided": 4,
    "Intellectual_disability|Spinocerebellar_ataxia_type_29": 1,
    "not_provided|Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome": 1,
    "ITPR1-related_disorder|not_specified": 2,
    "not_provided|Gillespie_syndrome": 3,
    "not_provided|not_specified|ITPR1-related_disorder": 1,
    "Spinocerebellar_ataxia_type_15/16|not_provided": 4,
    "ITPR1-related_syndromic_and_non-syndromic_hereditary_ataxias|Spinocerebellar_ataxia_type_29": 1,
    "not_provided|not_specified|Autosomal_dominant_cerebellar_ataxia": 5,
    "ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|See_cases|Intellectual_disability": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|not_provided|Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome": 2,
    "ITPR1-related_disorder|Inborn_genetic_diseases|Gillespie_syndrome|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Inborn_genetic_diseases": 1,
    "ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided": 1,
    "ITPR1-related_disorder|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "Slurred_speech|Progressive_gait_ataxia|Atypical_behavior|Movement_disorder": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|not_provided": 1,
    "not_provided|Spastic_ataxia": 3,
    "Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_provided": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_15/16|not_provided": 1,
    "not_provided|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_specified": 2,
    "Spinocerebellar_ataxia_type_29|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome|not_provided|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|ITPR1-related_disorder": 2,
    "not_provided|ITPR1-related_disorder": 11,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16": 1,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided": 9,
    "Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "Gillespie_syndrome|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Spinocerebellar_ataxia_type_15/16": 1,
    "ITPR1-related_disorder|not_specified|not_provided": 2,
    "Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|not_specified|not_provided|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "not_provided|ITPR1-related_disorder|not_specified": 2,
    "not_specified|Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Autosomal_dominant_cerebellar_ataxia|not_provided": 1,
    "Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome|ITPR1-related_disorders": 1,
    "ITPR1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Spinocerebellar_ataxia_type_15/16|Autosomal_dominant_cerebellar_ataxia|Intellectual_disability": 1,
    "Gillespie_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_15/16|not_provided|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_29|Neurodevelopmental_disorder|not_provided|Spinocerebellar_ataxia_type_15/16|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|not_provided|ITPR1-related_disorder": 2,
    "ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Intellectual_disability": 1,
    "not_specified|ITPR1-related_disorder|not_provided": 1,
    "not_provided|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_specified": 1,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_29": 1,
    "Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome": 1,
    "Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16": 1,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16|not_provided": 1,
    "Gillespie_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_provided": 1,
    "ITPR1-related_syndromic_and_non-syndromic_hereditary_ataxias|not_provided|ITPR1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_provided|not_specified": 1,
    "Bilateral_congenital_mydriasis": 1,
    "Autosomal_dominant_cerebellar_ataxia|Multiple_sclerosis|ITPR1-related_disorder|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_29|Spinocerebellar_ataxia_type_15/16": 1,
    "Inborn_genetic_diseases|Gillespie_syndrome|Autosomal_dominant_cerebellar_ataxia": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|Spinocerebellar_ataxia_type_29|ITPR1-related_disorder": 1,
    "ITPR1-related_disorder|not_provided|not_specified": 1,
    "not_provided|ITPR1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia": 2,
    "Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|not_provided|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia": 1,
    "ITPR1-related_syndromic_and_non-syndromic_hereditary_ataxias": 1,
    "ITPR1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|ITPR1-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_provided": 1,
    "ITPR1-related_disorder|not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_29": 1,
    "not_provided|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome|Spinocerebellar_ataxia_type_29|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Gillespie_syndrome": 1,
    "Gillespie_syndrome|Spinocerebellar_ataxia_type_15/16|Spinocerebellar_ataxia_type_29|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_29|Gillespie_syndrome|Anterior_segment_dysgenesis": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|Spinocerebellar_ataxia_type_29|not_provided|Spinocerebellar_ataxia_type_15/16|Gillespie_syndrome": 1,
    "ITPR1-related_disorder|Gillespie_syndrome|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "ITPR1-associated_cerebellar_ataxia_spectrum_disorder|not_provided|Spinocerebellar_ataxia_type_29": 1,
    "Inborn_genetic_diseases|Gillespie_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "GRM7-related_disorder|not_provided": 5,
    "Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities": 8,
    "GRM7-related_disorder": 2,
    "Global_developmental_delay|Hypotonia|Brain_atrophy|Seizure|Hypoplasia_of_the_corpus_callosum|Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities": 1,
    "Bilateral_multifocal_epileptiform_discharges|Global_developmental_delay|Microcephaly": 1,
    "Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Intellectual_disability|CNS_hypomyelination|Hypotonia|Brain_atrophy|Seizure|Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities": 1,
    "Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities|not_provided": 2,
    "Hypotonia|Seizure|Brain_atrophy|Intellectual_disability|CNS_hypomyelination|Global_developmental_delay|Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_seizures|_hypotonia|_and_brain_imaging_abnormalities|not_provided": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome|not_specified|not_provided|Caveolinopathy|Tip-toe_gait": 1,
    "not_specified|Congenital_long_QT_syndrome|Limb-Girdle_Muscular_Dystrophy|_Dominant|Caveolinopathy": 1,
    "CAV3-related_disorder|not_provided": 2,
    "CAV3-related_disorder|Long_QT_syndrome|not_specified": 1,
    "not_provided|Long_QT_syndrome|Elevated_circulating_creatine_kinase_concentration|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype": 917,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 112,
    "Long_QT_syndrome_9": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Caveolinopathy|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified": 25,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 38,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 84,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Rippling_muscle_disease_2": 1,
    "Cardiovascular_phenotype|CAV3-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|not_specified": 6,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Long_QT_syndrome": 2,
    "not_provided|Long_QT_syndrome_9": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome": 968,
    "Long_QT_syndrome|not_provided": 257,
    "Long_QT_syndrome|not_specified": 73,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 70,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Rippling_muscle_disease_2|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome": 303,
    "Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9|Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|not_provided|Long_QT_syndrome": 1,
    "CAV3-related_disorder|not_provided|Long_QT_syndrome": 2,
    "not_provided|Rippling_muscle_disease_2": 4,
    "not_provided|Long_QT_syndrome|Elevated_circulating_creatine_kinase_concentration": 1,
    "not_provided|Long_QT_syndrome_9|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Distal_myopathy|_Tateyama_type": 1,
    "Cardiovascular_phenotype|Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Caveolinopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Long_QT_syndrome|Rippling_muscle_disease_2": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided": 7,
    "Rippling_muscle_disease_2|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|not_provided|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome": 71,
    "not_specified|not_provided|Long_QT_syndrome": 17,
    "CAV3-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Caveolinopathy|Rippling_muscle_disease_2": 1,
    "Long_QT_syndrome|Elevated_circulating_creatine_kinase_concentration|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Rippling_muscle_disease_2": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 21,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 67,
    "not_provided|Elevated_circulating_creatine_kinase_concentration": 1,
    "Myopathy_with_tubular_aggregates|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Rippling_muscle_disease_2|Elevated_circulating_creatine_kinase_concentration": 1,
    "Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified": 24,
    "not_provided|Long_QT_syndrome|Caveolinopathy": 1,
    "Long_QT_syndrome|not_provided|not_specified": 6,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Cardiovascular_phenotype|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Long_QT_syndrome|Caveolinopathy|Cardiomyopathy|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Long_QT_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|Limb-Girdle_Muscular_Dystrophy|_Dominant|not_specified|not_provided|Long_QT_syndrome|Caveolinopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Rippling_muscle_disease_2|Elevated_circulating_creatine_kinase_concentration|Distal_myopathy|_Tateyama_type|Long_QT_syndrome|not_provided": 1,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|Caveolinopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Caveolinopathy": 1,
    "CAV3-related_disorder|not_specified|not_provided|Caveolinopathy|Long_QT_syndrome|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9|Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|CAV3-related_disorder|Cardiovascular_phenotype|not_specified|Limb-girdle_muscular_dystrophy|Long_QT_syndrome|not_provided|Caveolinopathy|Cardiomyopathy|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome|not_provided|Rippling_muscle_disease_2|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|CAV3-related_disorder|not_specified|not_provided|Long_QT_syndrome|Caveolinopathy|Cardiomyopathy|Long_QT_syndrome_9|Long_QT_syndrome_2/9|_digenic|Long_QT_syndrome_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|CAV3-related_disorder|not_provided|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_9": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Long_QT_syndrome|Long_QT_syndrome_1|See_cases": 1,
    "Long_QT_syndrome|Rippling_muscle_disease_2|Hypertrophic_cardiomyopathy_1|Distal_myopathy|_Tateyama_type|Long_QT_syndrome_9|Elevated_circulating_creatine_kinase_concentration": 1,
    "Hypertrophic_cardiomyopathy_1|Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Rippling_muscle_disease_2|Long_QT_syndrome|not_provided": 1,
    "CAV3-related_disorder|Long_QT_syndrome": 1,
    "Caveolinopathy|Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome": 5,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Rippling_muscle_disease_2|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 58,
    "not_specified|Long_QT_syndrome|Cardiomyopathy|not_provided|CAV3-related_disorder|Cardiovascular_phenotype|Caveolinopathy": 1,
    "Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9|Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Caveolinopathy|Rippling_muscle_disease_2|_autosomal_recessive": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 21,
    "not_provided|Caveolinopathy|Rippling_muscle_disease_2|Elevated_circulating_creatine_kinase_concentration": 1,
    "not_provided|Long_QT_syndrome_9|_acquired|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_1|Elevated_circulating_creatine_kinase_concentration|Rippling_muscle_disease_2|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type": 1,
    "Joubert_syndrome_9": 18,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|CAV3-related_disorder|Long_QT_syndrome": 1,
    "Hypertrophic_cardiomyopathy_1|Distal_myopathy|_Tateyama_type|Rippling_muscle_disease_2|Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9": 1,
    "not_provided|Long_QT_syndrome|Rippling_muscle_disease_2": 1,
    "Hypertrophic_cardiomyopathy_1|Long_QT_syndrome": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Rippling_muscle_disease_2|Elevated_circulating_creatine_kinase_concentration|Cardiovascular_phenotype|Cardiomyopathy|Long_QT_syndrome|Caveolinopathy": 1,
    "Cardiomyopathy|Long_QT_syndrome|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided|CAV3-related_disorder": 1,
    "Rippling_muscle_disease_2|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Elevated_circulating_creatine_kinase_concentration|Distal_myopathy|_Tateyama_type|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome": 21,
    "Cardiovascular_phenotype|Rippling_muscle_disease_2|Elevated_circulating_creatine_kinase_concentration|Distal_myopathy|_Tateyama_type|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|not_provided|Cardiomyopathy|Long_QT_syndrome": 1,
    "CAV3-related_disorder|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Cardiovascular_phenotype|Caveolinopathy|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|CAV3-related_disorder": 1,
    "Long_QT_syndrome_9|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|Hypertrophic_cardiomyopathy_1|Elevated_circulating_creatine_kinase_concentration|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Caveolinopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|CAV3-related_disorder|not_specified|not_provided|Caveolinopathy|Cardiomyopathy|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|not_specified": 6,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided": 5,
    "Caveolinopathy": 7,
    "not_specified|not_provided|Caveolinopathy|Cardiovascular_phenotype": 1,
    "not_provided|Caveolinopathy": 2,
    "Caveolinopathy|not_specified": 1,
    "Caveolinopathy|Hypertrophic_cardiomyopathy_1|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Long_QT_syndrome_9|Rippling_muscle_disease_2": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|not_provided|Caveolinopathy|Congenital_long_QT_syndrome": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Caveolinopathy|Congenital_long_QT_syndrome": 3,
    "Caveolinopathy|not_provided": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome|not_provided|Caveolinopathy": 4,
    "Caveolinopathy|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome_9|Rippling_muscle_disease_2|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome": 1,
    "Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Caveolinopathy": 1,
    "Hypertrophic_cardiomyopathy|Congenital_long_QT_syndrome|Long_QT_syndrome|Limb-Girdle_Muscular_Dystrophy|_Dominant|Caveolinopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Caveolinopathy|Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome": 2,
    "not_provided|Caveolinopathy|Limb-Girdle_Muscular_Dystrophy|_Dominant|Congenital_long_QT_syndrome": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Hypertrophic_cardiomyopathy_1|Rippling_muscle_disease_2|Long_QT_syndrome_9|Distal_myopathy|_Tateyama_type|Elevated_circulating_creatine_kinase_concentration|Caveolinopathy|Congenital_long_QT_syndrome": 1,
    "not_provided|OXTR-related_disorder": 2,
    "OXTR-related_disorder": 4,
    "SRGAP3-related_disorder|not_provided": 8,
    "SRGAP3-related_disorder": 9,
    "not_provided|SRGAP3-related_disorder": 12,
    "not_specified|not_provided|SRGAP3-related_disorder": 1,
    "SETD5-related_disorder": 20,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 125,
    "SETD5-related_syndromic_intellectual_disability": 1,
    "not_provided|SETD5-related_disorder": 13,
    "SETD5-related_disorder|not_provided": 12,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|not_provided": 29,
    "not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|Inborn_genetic_diseases": 3,
    "not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 18,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|SETD5-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|SETD5-related_disorder": 2,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_4": 25,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|SETD5-related_disorder|not_provided": 1,
    "Moyamoya_angiopathy_with_developmental_delay|not_provided": 2,
    "Neurodevelopmental_disorder|not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "not_provided|See_cases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "Chromatinopathy": 7,
    "Inborn_genetic_diseases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 4,
    "Developmental_disorder|not_provided": 6,
    "Inborn_genetic_diseases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 3,
    "Neurodevelopmental_abnormality|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "not_provided|SETD5-related_disorder|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|SETD5-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "SETD5-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Moyamoya_angiopathy_with_developmental_delay": 7,
    "not_specified|SETD5-related_disorder|not_provided": 1,
    "SETD5-related_disorder|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "Cleft_palate|Intellectual_disability|Cleft_lip": 1,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|Intellectual_disability": 1,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|Hearing_impairment|Global_developmental_delay|Heart|_malformation_of": 1,
    "SETD5-related_disorder|Moyamoya_angiopathy_with_developmental_delay|not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|Neurodevelopmental_disorder": 1,
    "Non-syndromic_intellectual_disability|Syndromic_intellectual_disability": 1,
    "Inborn_genetic_diseases|Intellectual_disability|See_cases|not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "not_specified|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "SETD5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "SETD5-related_disorder|not_provided|Inborn_genetic_diseases|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|Developmental_disorder|Cornelia_de_Lange-like_syndrome|not_provided": 1,
    "not_provided|NK-cell_enteropathy": 1,
    "Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|SETD5-related_disorder|not_provided": 3,
    "SETD5-related_disorder|not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 1,
    "Inborn_genetic_diseases|Microcephaly|not_provided": 2,
    "SETD5-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency": 2,
    "SETD5-related_disorder|Intellectual_disability-facial_dysmorphism_syndrome_due_to_SETD5_haploinsufficiency|not_provided": 1,
    "Inborn_genetic_diseases|SETD5-related_disorder|not_specified": 1,
    "not_provided|MTMR14-related_disorder": 2,
    "Autosomal_dominant_centronuclear_myopathy|not_provided": 3,
    "MTMR14-related_disorder|not_provided": 3,
    "MYOPATHY|_CENTRONUCLEAR|_AUTOSOMAL_DOMINANT|_MODIFIER_OF|not_provided": 1,
    "MTMR14-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_centronuclear_myopathy": 3,
    "Autosomal_dominant_centronuclear_myopathy": 31,
    "not_provided|MYOPATHY|_CENTRONUCLEAR|_AUTOSOMAL_DOMINANT|_MODIFIER_OF": 1,
    "MTMR14-related_disorder": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis": 86,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis": 2,
    "BRPF1-related_disorder": 19,
    "not_provided|BRPF1-related_disorder": 6,
    "BRPF1-related_disorder|not_provided": 3,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|not_provided": 4,
    "not_provided|BRPF1-related_disorder|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|Intellectual_disability": 1,
    "Sudden_unexplained_death_in_childhood|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|not_provided|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|not_provided": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|BRPF1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|See_cases": 1,
    "Autistic_behavior|Neurodevelopmental_delay": 1,
    "not_specified|BRPF1-related_disorder": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|Inborn_genetic_diseases|not_specified": 1,
    "BRPF1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|BRPF1-related_disorder|Inborn_genetic_diseases": 1,
    "Neurofibromatosis|_type_1": 6914,
    "not_specified|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|not_provided": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies_and_ptosis|Inborn_genetic_diseases|not_provided": 1,
    "Clear_cell_carcinoma_of_kidney|not_provided": 1,
    "OGG1-related_disorder": 5,
    "OGG1-related_disorder|not_provided": 1,
    "not_provided|OGG1-related_disorder": 1,
    "Nonpapillary_renal_cell_carcinoma": 4,
    "Developmental_delay|_language_impairment|_and_ocular_abnormalities|not_provided|Inborn_genetic_diseases": 1,
    "CIDEC-related_familial_partial_lipodystrophy": 2,
    "CIDEC-related_disorder": 2,
    "not_provided|CIDEC-related_disorder": 2,
    "not_provided|not_specified|CIDEC-related_disorder": 1,
    "not_specified|not_provided|CIDEC-related_disorder": 2,
    "not_provided|not_specified|CIDEC-related_familial_partial_lipodystrophy": 1,
    "not_provided|CIDEC-related_disorder|not_specified": 1,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency": 7,
    "Severe_congenital_neutropenia|Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency|not_provided": 3,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency|Inborn_genetic_diseases": 5,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency": 94,
    "Severe_congenital_neutropenia|Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency": 7,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency|Severe_congenital_neutropenia": 2,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency|not_provided": 3,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency|JAGN1-related_disorder": 3,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_JAGN1_deficiency|not_specified": 1,
    "JAGN1-related_disorder": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 91,
    "Candidiasis|_familial|_9": 629,
    "not_provided|Candidiasis|_familial|_9|IL17RC-related_disorder": 1,
    "not_provided|Candidiasis|_familial|_9": 9,
    "Candidiasis|_familial|_9|not_specified": 43,
    "not_specified|Candidiasis|_familial|_9": 27,
    "IL17RC-related_disorder|Candidiasis|_familial|_9": 4,
    "Candidiasis|_familial|_9|not_provided|IL17RC-related_disorder": 1,
    "Candidiasis|_familial|_9|IL17RC-related_disorder|not_provided": 2,
    "not_provided|not_specified|Candidiasis|_familial|_9": 1,
    "Candidiasis|_familial|_9|not_provided|not_specified": 8,
    "Candidiasis|_familial|_9|not_provided": 19,
    "not_specified|not_provided|IL17RC-related_disorder|Candidiasis|_familial|_9": 1,
    "IL17RC-related_disorder": 1,
    "IL17RC-related_disorder|Candidiasis|_familial|_9|not_provided": 1,
    "not_specified|not_provided|Candidiasis|_familial|_9": 1,
    "IL17RC-related_disorder|not_provided|Candidiasis|_familial|_9": 2,
    "Inborn_genetic_diseases|CRELD1-related_disorder": 1,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|not_specified": 1,
    "not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2": 6,
    "Atrioventricular_septal_defect|_susceptibility_to|_2": 67,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|Inborn_genetic_diseases": 2,
    "Congenital_heart_defects|_multiple_types|_4": 68,
    "not_provided|CRELD1-related_disorder": 1,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|not_provided": 4,
    "Inborn_genetic_diseases|Atrioventricular_septal_defect|_susceptibility_to|_2": 3,
    "not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2|Atrioventricular_septal_defect|_partial|_with_heterotaxy_syndrome": 1,
    "CRELD1-related_disorder": 6,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|not_provided|CRELD1-related_disorder|not_specified": 1,
    "CRELD1-related_disorder|Atrioventricular_septal_defect|_susceptibility_to|_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2|CRELD1-related_disorder": 1,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|Inborn_genetic_diseases|not_provided": 1,
    "Jeffries-Lakhani_neurodevelopmental_syndrome|Inborn_genetic_diseases|not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2|CRELD1-related_disorder": 1,
    "Ventricular_septal_defect_1": 7,
    "CRELD1-related_disorder|Inborn_genetic_diseases|Atrioventricular_septal_defect|_susceptibility_to|_2": 1,
    "Inborn_genetic_diseases|not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2": 2,
    "CRELD1-related_disorder|Atrioventricular_septal_defect|_susceptibility_to|_2": 4,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|CRELD1-related_disorder": 2,
    "Jeffries-Lakhani_neurodevelopmental_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Atrioventricular_septal_defect|_susceptibility_to|_2": 2,
    "not_specified|Atrioventricular_septal_defect|_susceptibility_to|_2|not_provided": 1,
    "not_specified|not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2": 2,
    "Inborn_genetic_diseases|not_provided|Atrioventricular_septal_defect|_susceptibility_to|_2|Jeffries-Lakhani_neurodevelopmental_syndrome|CRELD1-related_disorder": 1,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Tetralogy_of_Fallot|Atrioventricular_septal_defect|_susceptibility_to|_2": 1,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|not_provided|CRELD1-related_disorder": 2,
    "Atrioventricular_septal_defect|_susceptibility_to|_2|CRELD1-related_disorder|not_provided": 1,
    "Jeffries-Lakhani_neurodevelopmental_syndrome": 2,
    "Fanconi_anemia_complementation_group_D2": 218,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 72,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|not_provided": 9,
    "not_specified|Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 101,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D2|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Fanconi_anemia|FANCD2-related_disorder|Fanconi_anemia_complementation_group_D2": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 1,
    "Fanconi_anemia|not_specified|FANCD2-related_disorder|not_provided|Fanconi_anemia_complementation_group_D2|Fanconi_anemia_complementation_group_A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_D2": 7,
    "Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|not_specified": 2,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|not_specified": 2,
    "Fanconi_anemia_complementation_group_D2|not_provided": 4,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 6,
    "FANCD2-related_disorder|not_provided|Fanconi_anemia|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 3,
    "not_provided|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 5,
    "Fanconi_anemia|Inborn_genetic_diseases|not_provided": 31,
    "not_provided|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "FANCD2-related_disorder|Fanconi_anemia": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 6,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia|not_specified": 4,
    "Fanconi_anemia|FANCD2-related_disorder": 10,
    "not_provided|Fanconi_anemia_complementation_group_D2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia": 2,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 9,
    "Fanconi_anemia_complementation_group_D2|not_provided|Fanconi_anemia": 9,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_D2|Inborn_genetic_diseases": 1,
    "Familial_cancer_of_breast|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "FANCD2-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "not_provided|FANCD2-related_disorder|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 3,
    "Fanconi_anemia|FANCD2-related_disorder|not_provided|not_specified": 1,
    "Fanconi_anemia_complementation_group_D2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Acute_myeloid_leukemia|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia|See_cases": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_D2": 4,
    "FANCD2-related_disorder": 10,
    "not_specified|Fanconi_anemia_complementation_group_D2": 3,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder|not_provided": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_D2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_D2|not_specified|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia|FANCD2-related_disorder": 1,
    "Fanconi_anemia_complementation_group_A|not_provided": 22,
    "Fanconi_anemia_complementation_group_A|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|not_provided": 1,
    "FANCD2-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|Ovarian_cancer|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_D2": 2,
    "Fanconi_anemia_complementation_group_D2|not_specified": 2,
    "Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder|not_provided": 1,
    "Fanconi_anemia_complementation_group_D2|not_specified|not_provided": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|not_specified|not_provided": 1,
    "FANCD2-related_disorder|not_specified|Fanconi_anemia": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_D2": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_D2|Inborn_genetic_diseases": 4,
    "not_specified|Fanconi_anemia_complementation_group_D2|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia_complementation_group_D2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Fanconi_anemia_complementation_group_D2|not_provided|Fanconi_anemia|not_specified": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_D2|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "VHL-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder|Fanconi_anemia|not_provided": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia|Inborn_genetic_diseases": 2,
    "Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome": 9,
    "Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|Inborn_genetic_diseases": 3,
    "VHL-related_disorder": 7,
    "FANCD2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Malignant_tumor_of_breast": 1,
    "FANCD2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia_complementation_group_D2|Inborn_genetic_diseases|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_D2": 4,
    "Fanconi_anemia_complementation_group_A|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D2|Fanconi_anemia|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D2": 3,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Ovarian_cancer": 2,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia|Ovarian_cancer": 1,
    "not_provided|Fanconi_anemia|not_specified": 6,
    "not_provided|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_A|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia_complementation_group_D2|Fanconi_anemia|not_provided": 2,
    "not_provided|Fanconi_anemia|FANCD2-related_disorder|Fanconi_anemia_complementation_group_D2": 2,
    "not_specified|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_D2": 2,
    "not_provided|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Fanconi_anemia_complementation_group_D2|Hepatoblastoma|not_specified|FANCD2-related_disorder|not_provided|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 3,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|not_specified|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|not_specified|Fanconi_anemia_complementation_group_D2": 1,
    "VHL-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder": 1,
    "not_provided|Fanconi_anemia_complementation_group_D2": 4,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_D2": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_D2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|not_specified": 1,
    "FANCD2-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|FANCD2-related_disorder|Fanconi_anemia_complementation_group_D2": 1,
    "not_provided|Fanconi_anemia_complementation_group_D2|Fanconi_anemia|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_D2|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|Fanconi_anemia|FANCD2-related_disorder|not_specified|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_D2|not_specified": 1,
    "Fanconi_anemia_complementation_group_D2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|FANCD2-related_disorder|Fanconi_anemia_complementation_group_D2|not_provided": 1,
    "Fanconi_anemia_complementation_group_D2|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia": 11,
    "Fanconi_anemia|Ovarian_cancer": 3,
    "not_specified|Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|Ovarian_cancer": 1,
    "Fasting_plasma_glucose_level_quantitative_trait_locus_6": 1,
    "FANCD2OS-related_disorder": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|Hepatoblastoma": 1,
    "FANCD2-related_disorder|Fanconi_anemia_complementation_group_D2": 1,
    "not_specified|Fanconi_anemia_complementation_group_D2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|not_provided": 1,
    "not_provided|Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_D2": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_D2|FANCD2-related_disorder": 1,
    "Fanconi_anemia|not_provided|Inborn_genetic_diseases": 31,
    "Fanconi_anemia|Ovarian_cancer|Fanconi_anemia_complementation_group_D2": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D2": 1,
    "Intellectual_disability|Global_developmental_delay|Cleft_palate|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_D2|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_D2|not_specified": 1,
    "FANCD2-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_D2": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 115,
    "Pancreatic_cysts|Renal_cyst": 1,
    "Von_Hippel-Lindau_syndrome": 328,
    "Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia|Pheochromocytoma": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided": 26,
    "Von_Hippel-Lindau_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 1,
    "Chuvash_polycythemia": 6,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 438,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome": 25,
    "Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 17,
    "Von_Hippel-Lindau_syndrome|not_specified|not_provided": 1,
    "not_specified|Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Von_Hippel-Lindau_syndrome|not_provided|Chuvash_polycythemia|VHL-related_disorder": 1,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 254,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided": 14,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_specified": 7,
    "VHL-related_disorder|not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 1,
    "not_specified|not_provided|Von_Hippel-Lindau_syndrome": 1,
    "not_specified|VHL-related_disorder": 1,
    "VHL-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Chuvash_polycythemia|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia|Pheochromocytoma|Von_Hippel-Lindau_syndrome|not_specified": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 11,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided": 6,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_specified|not_provided": 2,
    "Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia": 13,
    "not_specified|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_provided": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 93,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 69,
    "Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 47,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 108,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 5,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 29,
    "Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 13,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 1,
    "not_specified|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided": 4,
    "Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 5,
    "Pheochromocytoma|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia": 4,
    "not_specified|Von_Hippel-Lindau_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Von_Hippel-Lindau_syndrome|not_provided|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 2,
    "not_specified|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 2,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|VHL-related_disorder": 4,
    "not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 11,
    "Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia|Pheochromocytoma|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Ovarian_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Maffucci_syndrome|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Chuvash_polycythemia|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|VHL-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided": 10,
    "Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 3,
    "Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 1,
    "not_provided|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 7,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_provided": 3,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome": 2,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Chuvash_polycythemia|Pheochromocytoma|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 2,
    "Von_Hippel-Lindau_syndrome|Pheochromocytoma|Chuvash_polycythemia|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|Enchondromatosis|not_specified|not_provided|Hepatoblastoma": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Von_Hippel-Lindau_syndrome|not_provided|Chuvash_polycythemia": 1,
    "Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|VHL-related_disorder|Chuvash_polycythemia|not_specified": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided|Pheochromocytoma": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Cerebellar_hemangioblastoma|Pancreatic_cysts|Retinal_capillary_hemangioma|Spinal_hemangioblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Chuvash_polycythemia": 1,
    "VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 3,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided": 1,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided": 9,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Polycythemia|not_provided": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Enchondromatosis|not_specified|not_provided|Hepatoblastoma": 1,
    "not_provided|Von_Hippel-Lindau_syndrome": 6,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|VHL-related_disorder": 1,
    "not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 5,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Tuberous_sclerosis_2": 1,
    "not_specified|not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 1,
    "VHL-related_disorder|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided|Pheochromocytoma": 2,
    "VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma": 1,
    "Von_Hippel-Lindau_syndrome|not_provided": 9,
    "Von_Hippel-Lindau_syndrome|VHL-related_disorder|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_provided": 1,
    "Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 2,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_specified|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|VHL-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Von_Hippel-Lindau_syndrome": 4,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "Von_Hippel-Lindau_syndrome|VHL-related_disorder|Chuvash_polycythemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_specified": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_provided|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_specified": 1,
    "VHL-related_disorder|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 5,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_specified": 1,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 4,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_specified|not_provided": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_specified": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder": 3,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Pheochromocytoma": 2,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|not_specified|VHL-related_disorder": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided|Congenital_Erythrocytosis": 1,
    "Von_Hippel-Lindau_syndrome|not_specified|Chuvash_polycythemia|not_provided": 1,
    "not_provided|not_specified|VHL-related_disorder|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "VHL-related_disorder|Von_Hippel-Lindau_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Von_Hippel-Lindau_syndrome|not_provided|Chuvash_polycythemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|not_provided": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_provided": 2,
    "not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 1,
    "Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 4,
    "Hereditary_cancer-predisposing_syndrome|VHL-related_disorder": 1,
    "not_provided|not_specified|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|See_cases|Chuvash_polycythemia": 1,
    "Lung_sarcomatoid_carcinoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_provided": 1,
    "not_provided|Pheochromocytoma|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_provided": 2,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "VHL-related_disorder|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_infantile_myasthenia": 1,
    "VHL-related_disorder|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|not_provided": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|RENAL_CELL_CARCINOMA_WITH_PARANEOPLASTIC_ERYTHROCYTOSIS": 1,
    "Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "Chuvash_polycythemia|not_provided|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 1,
    "Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma": 1,
    "Von_Hippel-Lindau_syndrome|Cerebellar_hemangioblastoma|Skin_adenoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Enchondromatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Von_Hippel-Lindau_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|not_provided": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pheochromocytoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Nonpapillary_renal_cell_carcinoma": 2,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|not_provided|VHL-related_disorder": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia": 1,
    "VHL-related_disorder|Au-Kline_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma": 1,
    "VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Pheochromocytoma|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided|Acute_leukemia_of_ambiguous_lineage": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Von_Hippel-Lindau_syndrome|not_specified|Chuvash_polycythemia": 1,
    "Maffucci_syndrome|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|VHL-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Nonpapillary_renal_cell_carcinoma|Pheochromocytoma|Chuvash_polycythemia|Von_Hippel-Lindau_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "VHL-related_disorder|not_provided|Von_Hippel-Lindau_syndrome": 1,
    "Von_Hippel-Lindau_syndrome|VHL-related_disorder|Chuvash_polycythemia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "TATDN2-related_disorder": 1,
    "not_provided|Inherited_obesity|Metabolic_syndrome|_susceptibility_to|Obesity|_age_at_onset_of|Obesity": 1,
    "Metabolic_syndrome|_susceptibility_to|Obesity": 1,
    "ATP2B2-related_disorder": 11,
    "not_provided|ATP2B2-related_disorder": 12,
    "Hearing_loss|_autosomal_dominant_82": 12,
    "not_provided|Hearing_loss|_autosomal_dominant_82": 1,
    "not_provided|ATP2B2-related_Progressive_hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified": 1,
    "not_provided|not_specified|Hearing_loss|_autosomal_dominant_82": 1,
    "not_provided|not_specified|ATP2B2-related_disorder": 1,
    "ATP2B2-related_disorder|not_provided": 7,
    "ATP2B2-related_disorder|not_provided|Deafness|_autosomal_recessive_12|_modifier_of|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 1,
    "not_specified|ATP2B2-related_disorder": 1,
    "Associated_with_severe_COVID-19_disease|not_provided": 2,
    "not_provided|Associated_with_severe_COVID-19_disease": 1,
    "not_specified|Hearing_loss|_autosomal_dominant_82": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_loss|_autosomal_dominant_82": 1,
    "Inborn_genetic_diseases|SLC6A1-related_disorder|not_provided": 1,
    "not_provided|Epilepsy_with_myoclonic_atonic_seizures": 36,
    "Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures": 21,
    "Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases|not_provided": 7,
    "SLC6A1-related_disorder|not_provided|Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases": 2,
    "SLC6A1-related_disorder": 8,
    "Epilepsy_with_myoclonic_atonic_seizures|not_provided|Inborn_genetic_diseases": 6,
    "Epilepsy_with_myoclonic_atonic_seizures|not_provided": 38,
    "Autosomal_dominant_epilepsy|Epilepsy_with_myoclonic_atonic_seizures|not_provided": 1,
    "SLC6A1-related_disorder|Inborn_genetic_diseases|not_provided|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases": 18,
    "Seizure|Global_developmental_delay": 2,
    "SLC6A1-related_disorder|Epilepsy_with_myoclonic_atonic_seizures": 4,
    "not_specified|not_provided|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder": 5,
    "not_provided|Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Epilepsy_with_myoclonic_atonic_seizures": 2,
    "Inborn_genetic_diseases|SLC6A1-related_disorder|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "not_specified|Epilepsy_with_myoclonic_atonic_seizures": 3,
    "Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases|SLC6A1-related_disorder|not_provided": 2,
    "Intellectual_disability|SLC6A1-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures": 4,
    "SLC6A1-related_neurodevelopmental_disorder|Epilepsy_with_myoclonic_atonic_seizures|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures|not_provided": 4,
    "Epilepsy_with_myoclonic_atonic_seizures|Intellectual_disability|not_provided": 1,
    "not_provided|Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases": 1,
    "not_specified|Epilepsy_with_myoclonic_atonic_seizures|Self-limited_epilepsy_with_centrotemporal_spikes": 1,
    "Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures|Autism_spectrum_disorder|not_provided": 1,
    "Intellectual_disability|See_cases|Epilepsy_with_myoclonic_atonic_seizures|not_provided": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Developmental_and_epileptic_encephalopathy_94": 1393,
    "Seizure|Intellectual_disability|SLC6A1-related_disorder|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_neurodevelopmental_condition|not_provided": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|not_specified|not_provided": 1,
    "not_provided|SLC6A1-related_disorder|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "not_provided|Neurodevelopmental_delay|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder|not_provided": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|not_specified": 4,
    "SLC6A1-related_disorder|Epilepsy_with_myoclonic_atonic_seizures|not_provided": 1,
    "not_specified|not_provided|Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases": 1,
    "not_provided|Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases|SLC6A1-related_disorder": 1,
    "not_provided|Epilepsy_with_myoclonic_atonic_seizures|Marfanoid_habitus_and_intellectual_disability": 1,
    "Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures|SLC6A1-related_disorder|not_provided": 1,
    "not_provided|Seizure|Neurodevelopmental_delay|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "SLC6A1-related_neurodevelopmental_disorder|Inborn_genetic_diseases|Epilepsy_with_myoclonic_atonic_seizures": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|not_provided|Intellectual_disability": 1,
    "SLC6A1-related_disorder|Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|not_provided|Global_developmental_delay": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases|not_specified": 1,
    "Epilepsy_with_myoclonic_atonic_seizures|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "SLC6A1-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_31": 14,
    "ATG7-related_disorder": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_31|NAFLD1": 1,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive_31|NAFLD1": 1,
    "not_provided|ATG7-related_disorder": 1,
    "not_specified|TAMM41-related_condition": 1,
    "Dysphagia|Bilateral_ptosis|Gastroesophageal_reflux|Respiratory_failure|Combined_oxidative_phosphorylation_deficiency_56": 1,
    "Combined_oxidative_phosphorylation_deficiency_56": 4,
    "Combined_oxidative_phosphorylation_deficiency_56|Abnormal_facial_shape|Proximal_muscle_weakness|Ankle_flexion_contracture|Neonatal_hypotonia|Bilateral_ptosis|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency_56|Dysphagia|Bilateral_ptosis|Gastroesophageal_reflux|Respiratory_failure": 1,
    "Abnormal_facial_shape|Proximal_muscle_weakness|Ankle_flexion_contracture|Neonatal_hypotonia|Bilateral_ptosis|Combined_oxidative_phosphorylation_deficiency_56|Combined_oxidative_phosphorylation_deficiency": 1,
    "SYN2-related_disorder": 7,
    "SYN2-related_disorder|not_provided": 1,
    "INSULIN_RESISTANCE|_DIGENIC|PPARG-related_familial_partial_lipodystrophy|Obesity": 2,
    "PPARG-related_disorder": 68,
    "PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|not_specified|not_provided|Obesity": 1,
    "PPARG-related_disorder|not_provided": 8,
    "PPARG-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    ".": 2307,
    "not_provided|PPARG-related_disorder": 14,
    "PPARG-related_disorder|Type_2_diabetes_mellitus|PPARG-related_familial_partial_lipodystrophy": 1,
    "not_specified|Obesity|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC": 1,
    "Obesity|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|PPARG-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|PPARG-related_disorder": 1,
    "Obesity|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC": 1,
    "PPARG-related_familial_partial_lipodystrophy": 24,
    "Type_2_diabetes_mellitus|PPARG-related_familial_partial_lipodystrophy|CAROTID_INTIMAL_MEDIAL_THICKNESS_1|Inherited_obesity|not_provided|Morbid_obesity": 1,
    "not_provided|PPARG-related_familial_partial_lipodystrophy": 2,
    "Type_2_diabetes_mellitus|PPARG-related_familial_partial_lipodystrophy": 1,
    "Obesity|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|not_specified|not_provided": 2,
    "PPARG-related_disorder|PPARG-related_familial_partial_lipodystrophy|Familial_partial_lipodystrophy|not_provided": 1,
    "INSULIN_RESISTANCE|_DIGENIC|PPARG-related_familial_partial_lipodystrophy|Type_2_diabetes_mellitus|not_provided|Obesity": 1,
    "Obesity|PPARG-related_disorder|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|Inborn_genetic_diseases": 1,
    "PPARG-related_disorder|Obesity|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|not_provided": 1,
    "PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|not_provided|Obesity": 1,
    "not_specified|PPARG-related_disorder|not_provided": 1,
    "DIABETES_MELLITUS|_TYPE_II|_DIGENIC|INSULIN_RESISTANCE|_DIGENIC": 1,
    "not_provided|CAROTID_INTIMAL_MEDIAL_THICKNESS_1|PPARG-related_familial_partial_lipodystrophy": 1,
    "INSULIN_RESISTANCE|_DIGENIC|PPARG-related_familial_partial_lipodystrophy|not_provided|Inborn_genetic_diseases|Obesity|not_specified": 1,
    "Inherited_obesity|Type_2_diabetes_mellitus|PPARG-related_familial_partial_lipodystrophy": 1,
    "PPARG-related_disorder|Carcinoma_of_colon": 1,
    "not_specified|not_provided|PPARG-related_disorder": 1,
    "not_provided|PPARG-related_disorder|Monogenic_diabetes|not_specified": 1,
    "PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|Obesity": 2,
    "not_provided|Lipodystrophy": 1,
    "INSULIN_RESISTANCE|_DIGENIC|PPARG-related_familial_partial_lipodystrophy|not_provided|Obesity": 1,
    "PPARG-related_disorder|PPARG-related_familial_partial_lipodystrophy|not_provided": 1,
    "PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC|CAROTID_INTIMAL_MEDIAL_THICKNESS_1|Type_2_diabetes_mellitus|Obesity|not_provided": 1,
    "not_provided|Glioma_susceptibility_1|INSULIN_RESISTANCE|_DIGENIC|PPARG-related_familial_partial_lipodystrophy|not_specified|PPARG_POLYMORPHISM|Obesity": 1,
    "not_specified|PPARG-related_disorder|not_provided|Obesity|PPARG-related_familial_partial_lipodystrophy|INSULIN_RESISTANCE|_DIGENIC": 1,
    "Lipodystrophy|PPARG-related_familial_partial_lipodystrophy|not_provided": 1,
    "Pontoneocerebellar_hypoplasia|not_provided": 40,
    "Pontoneocerebellar_hypoplasia": 108,
    "TSEN2-related_disorder|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_2B": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_2B": 2,
    "not_specified|TSEN2-related_disorder|not_provided": 1,
    "not_provided|not_specified|TSEN2-related_disorder|Pontoneocerebellar_hypoplasia": 2,
    "Inborn_genetic_diseases|Pontoneocerebellar_hypoplasia": 2,
    "not_specified|not_provided|Pontoneocerebellar_hypoplasia": 5,
    "Pontocerebellar_hypoplasia_type_2B": 16,
    "Pontoneocerebellar_hypoplasia|not_provided|not_specified": 7,
    "Pontoneocerebellar_hypoplasia|not_specified|not_provided": 9,
    "not_provided|TSEN2-related_disorder": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_2B|not_provided|Pontoneocerebellar_hypoplasia": 1,
    "not_provided|Pontoneocerebellar_hypoplasia|not_specified": 7,
    "Pontocerebellar_hypoplasia_type_2B|Pontoneocerebellar_hypoplasia": 2,
    "Pontocerebellar_hypoplasia_type_2B|not_specified|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "not_provided|TSEN2-related_disorder|Pontoneocerebellar_hypoplasia": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_2B": 1,
    "TSEN2-related_disorder|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "TSEN2-related_disorder|Pontoneocerebellar_hypoplasia|not_specified|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_2B|not_provided": 2,
    "Pontoneocerebellar_hypoplasia|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Pontoneocerebellar_hypoplasia": 1,
    "TSEN2-related_disorder": 2,
    "Pontocerebellar_hypoplasia_type_2B|TSEN2-related_disorder|Pontoneocerebellar_hypoplasia|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Pontoneocerebellar_hypoplasia|not_provided": 3,
    "Pontocerebellar_hypoplasia_type_2B|not_provided|Pontoneocerebellar_hypoplasia": 1,
    "Pontoneocerebellar_hypoplasia|not_specified": 2,
    "Pontocerebellar_hypoplasia_type_2B|not_provided|Inborn_genetic_diseases": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Pontocerebellar_hypoplasia_type_2B": 1,
    "not_provided|Pontoneocerebellar_hypoplasia": 14,
    "not_provided|Hemolytic-uremic_syndrome": 1,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 54,
    "Pontocerebellar_hypoplasia_type_2B|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_2B|not_provided": 1,
    "Noonan_syndrome_5|LEOPARD_syndrome_2": 20,
    "Noonan_syndrome|not_provided|Noonan_syndrome_with_multiple_lentigines": 2,
    "Dilated_cardiomyopathy_1NN|LEOPARD_syndrome_2|Noonan_syndrome_5": 1,
    "Noonan_syndrome_5|not_provided|LEOPARD_syndrome_2": 2,
    "Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided": 1,
    "not_provided|LEOPARD_syndrome_2|Noonan_syndrome_5": 1,
    "LEOPARD_syndrome_2|Noonan_syndrome_5": 6,
    "not_provided|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 5,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1NN|not_provided|RASopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|LEOPARD_syndrome_2|Noonan_syndrome_5": 1,
    "Cardiovascular_phenotype|RAF1-related_disorder|RASopathy": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|LEOPARD_syndrome_2|Noonan_syndrome_5|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_5": 1,
    "RAF1-related_disorder": 11,
    "Dilated_cardiomyopathy_1NN|RASopathy|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome_5": 1,
    "not_provided|Inborn_genetic_diseases|RASopathy": 1,
    "not_provided|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|RASopathy": 1,
    "LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|RASopathy|not_provided": 1,
    "Noonan_syndrome_5|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_5|RASopathy": 1,
    "Hypertrophic_cardiomyopathy_1|RAF1-related_disorder|not_provided|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|LEOPARD_syndrome_2|Noonan_syndrome_5|RASopathy": 1,
    "RAF1-related_disorder|Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "Cardiovascular_phenotype|not_specified|RAF1-related_disorder|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN|not_specified|not_provided|RASopathy": 1,
    "Dilated_cardiomyopathy_1NN": 5,
    "RASopathy|not_specified|RAF1-related_disorder": 1,
    "not_provided|Dilated_cardiomyopathy_1NN|LEOPARD_syndrome_2|Noonan_syndrome_5|RASopathy|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer|RAF1-related_disorder|Cardiovascular_phenotype|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|not_specified|not_provided|RASopathy|Noonan_syndrome|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "RAF1-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy": 1,
    "RASopathy|not_specified|not_provided|Cardiovascular_phenotype": 5,
    "RASopathy|RAF1-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2|not_specified|RASopathy": 1,
    "RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|RAF1-related_disorder|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|RASopathy": 3,
    "RASopathy|not_provided|not_specified|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|RASopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|LEOPARD_syndrome_2|Noonan_syndrome_5|Cardiovascular_phenotype|RAF1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Cardiovascular_phenotype": 2,
    "RAF1-related_disorder|not_specified|RASopathy|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_5": 9,
    "Cardiovascular_phenotype|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|not_specified|RASopathy": 1,
    "RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_5|not_provided|RASopathy": 1,
    "RASopathy|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|LEOPARD_syndrome_2": 1,
    "Noonan_syndrome|not_provided|RASopathy|RAF1-related_disorder": 1,
    "Noonan_syndrome_with_multiple_lentigines": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|RASopathy": 3,
    "RASopathy|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|not_provided|Noonan_syndrome": 1,
    "RASopathy|Noonan_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Cardiovascular_phenotype": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "RASopathy|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_5|RASopathy": 1,
    "RASopathy|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN|Noonan_syndrome_5|not_provided": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_5": 1,
    "Cardiovascular_phenotype|RASopathy|RAF1-related_disorder": 1,
    "Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|RASopathy|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN": 1,
    "RAF1-related_disorder|RASopathy|Noonan_syndrome|not_specified|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome|Noonan_syndrome_5|not_provided|LEOPARD_syndrome_2|RASopathy": 1,
    "RASopathy|Noonan_syndrome|not_specified": 1,
    "RAF1-related_disorder|RASopathy": 2,
    "RASopathy|RAF1-related_disorder": 3,
    "Hypertrophic_cardiomyopathy_1|not_specified|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome_5|LEOPARD_syndrome_2|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "RASopathy|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "not_specified|LEOPARD_syndrome_2|not_provided|Noonan_syndrome_5|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome": 2,
    "RAF1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|LEOPARD_syndrome_2|Noonan_syndrome_5|Cardiovascular_phenotype|RASopathy|not_provided|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|not_provided|RAF1-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy": 6,
    "RASopathy|Cardiovascular_phenotype|not_specified": 20,
    "RASopathy|Cardiovascular_phenotype|RAF1-related_disorder": 1,
    "not_provided|not_specified|RASopathy": 4,
    "Cardiovascular_phenotype|RAF1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_5|not_provided|not_specified|RASopathy": 1,
    "not_specified|RAF1-related_disorder": 1,
    "LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome_5": 1,
    "not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_1": 4,
    "RASopathy|Cardiovascular_phenotype|not_provided|Noonan_syndrome_5": 1,
    "Noonan_syndrome_3|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Noonan_syndrome": 1,
    "Noonan_syndrome_5|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1NN|Noonan_syndrome|RASopathy": 1,
    "not_provided|Noonan_syndrome|Noonan_syndrome_5|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_5|Noonan_syndrome_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "RAF1-related_disorder|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_5|Primary_familial_hypertrophic_cardiomyopathy|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN": 1,
    "RASopathy|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "RASopathy|Noonan_syndrome_5": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "not_provided|Noonan_syndrome_5|RASopathy": 1,
    "Noonan_syndrome_5|LEOPARD_syndrome_2|RASopathy|not_specified|Noonan_syndrome|not_provided": 1,
    "LEOPARD_syndrome_2": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RAF1-related_disorder|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|Dilated_cardiomyopathy_1NN|Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided|RASopathy|Noonan_syndrome_1|See_cases": 1,
    "Cardiovascular_phenotype|RASopathy|Noonan_syndrome_5": 1,
    "not_provided|RASopathy|Noonan_syndrome|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Noonan_syndrome_5|Noonan_syndrome|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "not_provided|RASopathy|Noonan_syndrome_1|Noonan_syndrome": 1,
    "not_specified|Dilated_cardiomyopathy_1NN|not_provided|RASopathy|Noonan_syndrome_5": 1,
    "RASopathy|not_specified|not_provided|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "Glioma": 1,
    "RASopathy|LEOPARD_syndrome_2|Noonan_syndrome_5": 1,
    "RASopathy|not_specified|RAF1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1NN|LEOPARD_syndrome_2|Noonan_syndrome_5|RASopathy|not_provided": 1,
    "not_specified|Noonan_syndrome_5|LEOPARD_syndrome_2|RASopathy": 1,
    "Trigonitis": 1,
    "not_specified|Cardiovascular_phenotype|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|RASopathy": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "Noonan_syndrome_5|Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome": 1,
    "RAF1-related_disorder|not_provided|Cardiovascular_phenotype|RASopathy": 1,
    "LEOPARD_syndrome_2|Noonan_syndrome_5|not_provided|Dilated_cardiomyopathy_1NN|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Cardiovascular_phenotype": 1,
    "RASopathy|not_provided|Noonan_syndrome_5|LEOPARD_syndrome_2|Cardiovascular_phenotype": 1,
    "RASopathy|not_provided|Noonan_syndrome": 2,
    "RASopathy|Noonan_syndrome|not_provided": 4,
    "Noonan_syndrome_5|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN|RAF1-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1NN|LEOPARD_syndrome_2|Noonan_syndrome_5|RAF1-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|RASopathy": 2,
    "RAF1-related_disorder|Cardiovascular_phenotype": 1,
    "RASopathy|Cardiovascular_phenotype|LEOPARD_syndrome_2": 1,
    "not_provided|not_specified|Noonan_syndrome_5|Cardiovascular_phenotype|RASopathy": 1,
    "not_specified|not_provided|RASopathy|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome": 1,
    "not_specified|LEOPARD_syndrome_2|Noonan_syndrome_5|RASopathy|not_provided": 1,
    "RASopathy|not_specified|Noonan_syndrome_and_Noonan-related_syndrome": 3,
    "Dilated_cardiomyopathy_1NN|not_provided": 1,
    "RASopathy|Noonan_syndrome_5|LEOPARD_syndrome_2|not_specified": 1,
    "not_specified|Noonan_syndrome|RASopathy|LEOPARD_syndrome_2|not_provided": 1,
    "RAF1-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy|not_specified": 1,
    "not_specified|RASopathy|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|RASopathy|Dilated_cardiomyopathy_1NN|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_5": 1,
    "LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN": 1,
    "RAF1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|RASopathy|Primary_dilated_cardiomyopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|not_provided|RASopathy|RAF1-related_disorder": 1,
    "not_provided|Noonan_syndrome|Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2|RAF1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 1,
    "Noonan_syndrome_5|LEOPARD_syndrome_2|Noonan_syndrome_1|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "RAF1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|RASopathy|not_specified": 1,
    "RASopathy|RAF1-related_disorder|not_specified": 1,
    "not_specified|RASopathy|Cardiovascular_phenotype|RAF1-related_disorder": 1,
    "RASopathy|LEOPARD_syndrome_2|Noonan_syndrome_5|See_cases": 1,
    "RAF1-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|RASopathy|Noonan_syndrome_5|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided|RASopathy|not_specified": 1,
    "RASopathy|RAF1-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_5|LEOPARD_syndrome_2": 1,
    "Noonan_syndrome_5|LEOPARD_syndrome_2|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome_5|LEOPARD_syndrome_2|Dilated_cardiomyopathy_1NN": 2,
    "Noonan_syndrome_5|Dilated_cardiomyopathy_1NN|LEOPARD_syndrome_2": 1,
    "LEOPARD_syndrome_2|not_provided|Noonan_syndrome_5|not_specified": 1,
    "RASopathy|Dilated_cardiomyopathy_1NN|Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided|not_specified": 1,
    "not_specified|LEOPARD_syndrome_2|Noonan_syndrome_5|Dilated_cardiomyopathy_1NN": 1,
    "RASopathy|not_specified|Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided": 1,
    "not_specified|Noonan_syndrome_5|LEOPARD_syndrome_2|not_provided": 1,
    "Dilated_cardiomyopathy_1NN|Noonan_syndrome_5|LEOPARD_syndrome_2|not_specified|RASopathy|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines": 1,
    "Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|not_specified|not_provided": 1,
    "IQSEC1-related_disorder": 3,
    "Intellectual_developmental_disorder_with_short_stature_and_behavioral_abnormalities": 9,
    "not_provided|IQSEC1-related_disorder": 1,
    "not_provided|Intellectual_developmental_disorder_with_short_stature_and_behavioral_abnormalities": 2,
    "Intellectual_developmental_disorder_with_short_stature_and_behavioral_abnormalities|not_specified": 4,
    "IQSEC1-related_disorder|not_provided": 1,
    "NUP210-related_disorder": 5,
    "not_provided|NUP210-related_disorder": 1,
    "not_provided|Fuhrmann_syndrome|Schinzel_phocomelia_syndrome|Santos_syndrome": 1,
    "WNT7A-related_disorder": 3,
    "Fuhrmann_syndrome|Santos_syndrome|Schinzel_phocomelia_syndrome|Inborn_genetic_diseases": 1,
    "Schinzel_phocomelia_syndrome": 6,
    "not_provided|Schinzel_phocomelia_syndrome|Fuhrmann_syndrome": 1,
    "WNT7A-related_disorder|not_provided": 3,
    "Fuhrmann_syndrome|not_provided": 1,
    "WNT7A-related_disorder|not_specified|not_provided": 2,
    "WNT7A-related_disoder": 1,
    "Fuhrmann_syndrome": 2,
    "Schinzel_phocomelia_syndrome|Fuhrmann_syndrome|not_provided": 1,
    "not_provided|WNT7A-related_disorder": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5": 382,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 3,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 6,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5": 36,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 38,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 33,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 36,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 7,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 2,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 19,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Cardiovascular_phenotype": 12,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 3,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiomyopathy": 5,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 7,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype|TMEM43-related_disorder": 1,
    "TMEM43-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5": 9,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy": 7,
    "not_provided|TMEM43-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 3,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Cardiomyopathy|not_specified": 1,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_specified": 12,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5": 2,
    "Cardiovascular_phenotype|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "TMEM43-related_disorder|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|TMEM43-related_disorder|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "TMEM43-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|TMEM43-related_disorder|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_specified": 2,
    "TMEM43-related_disorder|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|not_provided|Cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|TMEM43-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|not_specified|not_provided|Cardiomyopathy": 1,
    "TMEM43-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "TMEM43-related_disorder|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "See_cases|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiovascular_phenotype|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 6,
    "Cardiovascular_phenotype|not_specified|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 9,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|TMEM43-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "TMEM43-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiovascular_phenotype|TMEM43-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_provided": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|TMEM43-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Sudden_cardiac_arrest": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Emery-Dreifuss_muscular_dystrophy_2|_autosomal_dominant": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_specified": 2,
    "not_provided|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|TMEM43-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "TMEM43-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "TMEM43-related_disorder|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|not_provided|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Cardiomyopathy": 1,
    "TMEM43-related_disorder|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|TMEM43-related_disorder|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "TMEM43-related_disorder|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|TMEM43-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Sudden_cardiac_arrest|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|TMEM43-related_disorder": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Hypertrophic_cardiomyopathy": 1,
    "not_specified|TMEM43-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "TMEM43-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_5": 1,
    "not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|Cardiomyopathy|TMEM43-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Auditory_neuropathy|_autosomal_dominant_3|Arrhythmogenic_right_ventricular_dysplasia_5|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_5|Auditory_neuropathy|_autosomal_dominant_3|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_5|Cardiomyopathy|Emery-Dreifuss_muscular_dystrophy_7|_autosomal_dominant|Auditory_neuropathy|_autosomal_dominant_3": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum": 8,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum": 3,
    "Xeroderma_pigmentosum|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Xeroderma_pigmentosum|_group_C": 125,
    "Xeroderma_pigmentosum|_group_C|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum": 3,
    "not_provided|Xeroderma_pigmentosum|_group_C": 39,
    "Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Xeroderma_pigmentosum|Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum|_group_C": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum|_group_C": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 1,
    "XPC-related_disorder|not_provided|Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum|not_specified": 1,
    "not_specified|Xeroderma_pigmentosum|_group_C": 1,
    "not_provided|XPC-related_disorder": 2,
    "Xeroderma_pigmentosum|_group_C|not_specified|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_C|not_specified|Inborn_genetic_diseases": 1,
    "XPC-related_disorder": 2,
    "not_specified|not_provided|Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum_group_A": 2,
    "Xeroderma_pigmentosum|_group_C|not_specified|not_provided|Xeroderma_pigmentosum_group_A": 1,
    "Xeroderma_pigmentosum|_group_C|Inborn_genetic_diseases": 4,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 4,
    "Xeroderma_pigmentosum|_group_C|not_provided": 37,
    "Xeroderma_pigmentosum|_group_C|not_specified": 9,
    "not_specified|Xeroderma_pigmentosum|_group_C|not_provided": 2,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 3,
    "Xeroderma_pigmentosum|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Xeroderma_pigmentosum|_group_C": 1,
    "Xeroderma_pigmentosum|_group_C|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum|_group_C": 1,
    "Inborn_genetic_diseases|Hereditary_cancer": 3,
    "XPC-related_disorder|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 1,
    "not_specified|not_provided|Xeroderma_pigmentosum_group_A|Xeroderma_pigmentosum|_group_C": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C|not_provided": 4,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum|_group_C": 5,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C|XPC-related_disorder": 1,
    "Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum|not_specified|not_provided": 2,
    "not_specified|Xeroderma_pigmentosum|_group_C|not_provided|Xeroderma_pigmentosum_group_A": 2,
    "Xeroderma_pigmentosum_group_A": 69,
    "not_provided|Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum": 2,
    "not_specified|XPC-related_disorder|not_provided|Xeroderma_pigmentosum|_group_C": 1,
    "Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|_group_C|not_specified": 1,
    "Xeroderma_pigmentosum|_group_C|not_provided|not_specified": 2,
    "Xeroderma_pigmentosum|_group_C|not_provided|Xeroderma_pigmentosum": 5,
    "Xeroderma_pigmentosum|_group_C|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum": 4,
    "XPC-related_disorder|not_provided|Xeroderma_pigmentosum|See_cases|Xeroderma_pigmentosum|_group_C": 1,
    "not_provided|Xeroderma_pigmentosum|_group_C|not_specified|XPC-related_disorder": 1,
    "Xeroderma_pigmentosum_group_A|not_provided|Xeroderma_pigmentosum|_group_C|not_specified": 2,
    "Xeroderma_pigmentosum_group_A|XPC-related_disorder|Xeroderma_pigmentosum|_group_C|not_provided|not_specified": 1,
    "not_specified|not_provided|Xeroderma_pigmentosum|_group_C": 1,
    "not_provided|Xeroderma_pigmentosum|_group_C|XPC-related_disorder": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_C": 2,
    "not_specified|Ovarian_cancer|Inborn_genetic_diseases": 1,
    "XPC-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_C|not_specified": 1,
    "not_specified|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 2,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum|_group_C|Inborn_genetic_diseases": 1,
    "not_provided|Xeroderma_pigmentosum|Familial_prostate_cancer|Xeroderma_pigmentosum|_group_C": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 1,
    "XPC-related_disorder|not_provided|not_specified|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_C": 1,
    "Xeroderma_pigmentosum|_group_C|not_provided|not_specified|Xeroderma_pigmentosum_group_A": 1,
    "not_provided|Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum_group_A|not_specified": 1,
    "Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum|not_provided": 3,
    "Xeroderma_pigmentosum|_group_C|Xeroderma_pigmentosum_group_A|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum|_group_C|Inborn_genetic_diseases|not_provided": 1,
    "Xeroderma_pigmentosum|_group_C|Inborn_genetic_diseases|Xeroderma_pigmentosum": 1,
    "not_provided|not_specified|Xeroderma_pigmentosum|_group_C": 1,
    "Xeroderma_pigmentosum_group_A|Xeroderma_pigmentosum|_group_C|not_provided|not_specified": 1,
    "Xeroderma_pigmentosum_group_A|Xeroderma_pigmentosum|_group_C|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum|not_specified|Xeroderma_pigmentosum|_group_C|not_provided": 1,
    "Xeroderma_pigmentosum|_group_C|not_specified|Xeroderma_pigmentosum_group_A|not_provided": 1,
    "Retinal_degeneration|Hypotaurinemic_retinal_degeneration_and_cardiomyopathy": 2,
    "Hypotaurinemic_retinal_degeneration_and_cardiomyopathy|not_specified": 1,
    "not_provided|Severe_hypotonia-psychomotor_developmental_delay-strabismus-cardiac_septal_defect_syndrome|not_specified": 1,
    "CCDC174-related_disorder": 2,
    "CCDC174-related_disorder|not_provided": 1,
    "Severe_hypotonia-psychomotor_developmental_delay-strabismus-cardiac_septal_defect_syndrome|not_provided": 3,
    "not_provided|CCDC174-related_disorder": 2,
    "not_provided|Severe_hypotonia-psychomotor_developmental_delay-strabismus-cardiac_septal_defect_syndrome": 2,
    "Severe_hypotonia-psychomotor_developmental_delay-strabismus-cardiac_septal_defect_syndrome": 3,
    "Severe_hypotonia-psychomotor_developmental_delay-strabismus-cardiac_septal_defect_syndrome|CCDC174-related_disorder|not_provided": 1,
    "not_specified|Severe_hypotonia-psychomotor_developmental_delay-strabismus-cardiac_septal_defect_syndrome": 1,
    "Combined_oxidative_phosphorylation_deficiency_50": 1,
    "RBSN-related_disorder": 1,
    "Kariminejad_neurodevelopmental_syndrome": 2,
    "Myelofibrosis|_congenital|_with_anemia|_neutropenia|_developmental_delay|_and_ocular_abnormalities": 1,
    "Congenital_myasthenic_syndrome_5": 375,
    "not_provided|Congenital_myasthenic_syndrome_5": 15,
    "Congenital_myasthenic_syndrome_5|not_provided": 7,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_5": 16,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_5": 3,
    "Congenital_myasthenic_syndrome_5|Inborn_genetic_diseases": 12,
    "Congenital_myasthenic_syndrome_5|COLQ-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_5|not_specified": 1,
    "Congenital_myasthenic_syndrome_5|not_provided|COLQ-related_disorder": 2,
    "Congenital_myasthenic_syndrome_5|Congenital_myasthenic_syndrome|COLQ-related_disorder|Slow-Channel_Congenital_Myasthenia_Syndrome": 1,
    "Synaptic_congenital_myasthenic_syndromes|Congenital_myasthenic_syndrome_5": 1,
    "not_provided|Congenital_myasthenic_syndrome_5|not_specified": 5,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_5|not_provided": 1,
    "not_specified|Congenital_myasthenic_syndrome_5": 4,
    "Congenital_myasthenic_syndrome_5|Synaptic_congenital_myasthenic_syndromes": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_5": 3,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_5|not_provided": 1,
    "Congenital_myasthenic_syndrome_5|not_provided|Congenital_myasthenic_syndrome|Abnormality_of_the_musculature": 1,
    "COLQ-related_disorder|Congenital_myasthenic_syndrome_5": 1,
    "Synaptic_congenital_myasthenic_syndromes": 3,
    "COLQ-related_disorder|not_specified|Congenital_myasthenic_syndrome_5": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_5|Synaptic_congenital_myasthenic_syndromes": 1,
    "Congenital_myasthenic_syndrome_5|Congenital_myasthenic_syndrome": 3,
    "Congenital_myasthenic_syndrome_5|Synaptic_congenital_myasthenic_syndromes|not_provided": 1,
    "Congenital_myasthenic_syndrome_5|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_myasthenic_syndrome_5|not_specified|not_provided": 3,
    "Congenital_myasthenic_syndrome_5|Congenital_myasthenic_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_5": 2,
    "Congenital_myasthenic_syndrome_5|COLQ-related_disorder": 3,
    "Congenital_myasthenic_syndrome_5|not_specified": 2,
    "Synaptic_congenital_myasthenic_syndromes|Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_5": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_5": 4,
    "not_specified|Congenital_myasthenic_syndrome_5|not_provided": 1,
    "See_cases|Congenital_myasthenic_syndrome_5": 1,
    "not_provided|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_5": 1,
    "Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_5": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_5": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_myasthenic_syndrome_5": 1,
    "Congenital_myasthenic_syndrome_5|COLQ-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|COLQ-related_disorder|Congenital_myasthenic_syndrome_5": 1,
    "Congenital_Myasthenic_Syndrome|_Recessive|not_provided": 3,
    "HACL1-related_disorder": 11,
    "not_provided|HACL1-related_disorder": 1,
    "not_provided|Biotinidase_deficiency": 53,
    "not_specified|not_provided|Biotinidase_deficiency": 7,
    "Biotinidase_deficiency": 469,
    "BTD-related_disorder": 5,
    "Biotinidase_deficiency|not_provided": 27,
    "Generalized_hypotonia|Global_developmental_delay|Cryptorchidism|Macrocephaly|Biotinidase_deficiency": 1,
    "Biotinidase_deficiency|BTD-related_disorder": 1,
    "Biotinidase_deficiency|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|Biotinidase_deficiency|Intellectual_disability": 1,
    "BTD-related_disorder|not_specified|not_provided|Biotinidase_deficiency": 1,
    "not_specified|Biotinidase_deficiency": 14,
    "BTD-related_disorder|not_provided|Biotinidase_deficiency": 5,
    "not_specified|Biotinidase_deficiency|not_provided": 1,
    "Biotinidase_deficiency|not_specified": 17,
    "Biotinidase_deficiency|not_provided|Inborn_genetic_diseases|BTD-related_disorder": 1,
    "Inborn_genetic_diseases|Biotinidase_deficiency": 4,
    "BTD-related_disorder|Biotinidase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Biotinidase_deficiency|not_provided": 2,
    "Biotinidase_deficiency|BTD-related_disorder|not_specified": 1,
    "not_provided|not_specified|Biotinidase_deficiency": 2,
    "not_provided|BTD-related_disorder|Inborn_genetic_diseases|Biotinidase_deficiency": 1,
    "Inborn_genetic_diseases|Biotinidase_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Biotinidase_deficiency": 6,
    "Inborn_genetic_diseases|Biotinidase_deficiency|not_specified": 2,
    "not_specified|Biotinidase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Biotinidase_deficiency|not_specified": 2,
    "not_specified|Biotinidase_deficiency|Intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "Biotinidase_deficiency|Intellectual_disability": 1,
    "Biotinidase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "BTD-related_disorder|Biotinidase_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Biotinidase_deficiency": 1,
    "Biotinidase_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "BTD-related_disorder|not_provided|not_specified|Biotinidase_deficiency": 1,
    "Biotinidase_deficiency|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|BTD-related_disorder": 1,
    "Possible_mitochondrial_disorder_-_nuclear_genes|BTD-related_disorder|Inborn_genetic_diseases|not_provided|Biotinidase_deficiency": 1,
    "Possible_mitochondrial_disorder_-_nuclear_genes|BTD-related_disorder|not_provided|Biotinidase_deficiency": 1,
    "BTD-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|Biotinidase_deficiency": 1,
    "BTD-related_disorder|Biotinidase_deficiency": 3,
    "not_specified|Biotinidase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Biotinidase_deficiency|BTD-related_disorder|not_provided": 2,
    "BTD-related_disorder|Inborn_genetic_diseases|not_provided|Biotinidase_deficiency": 2,
    "not_specified|Biotinidase_deficiency|BTD-related_disorder": 1,
    "DAZL-related_disorder": 6,
    "Idiopathic_male_infertility": 6,
    "Reclassified_-_variant_of_unknown_significance": 1,
    "TBC1D5-related_disorder": 4,
    "Developmental_delay_with_dysmorphic_facies_and_dental_anomalies": 22,
    "Kohlschutter-Tonz_syndrome-like": 6,
    "SATB1-related_disorder": 11,
    "Developmental_delay_with_dysmorphic_facies_and_dental_anomalies|not_provided": 2,
    "SATB1-related_disorder|not_provided": 1,
    "Kohlschutter-Tonz_syndrome-like|Developmental_delay_with_dysmorphic_facies_and_dental_anomalies": 2,
    "not_provided|Kohlschutter-Tonz_syndrome-like": 2,
    "not_provided|Developmental_delay_with_dysmorphic_facies_and_dental_anomalies": 2,
    "Developmental_delay_with_dysmorphic_facies_and_dental_anomalies|Kohlschutter-Tonz_syndrome-like": 2,
    "not_specified|Developmental_delay_with_dysmorphic_facies_and_dental_anomalies|not_provided": 1,
    "not_specified|Kohlschutter-Tonz_syndrome-like": 1,
    "Kohlschutter-Tonz_syndrome-like|Inborn_genetic_diseases": 1,
    "Kohlschutter-Tonz_syndrome-like|SATB1-related_disorder": 1,
    "not_provided|SATB1-related_disorder": 2,
    "SATB1-related_neurodevelopmental_disorder": 1,
    "Action_myoclonus-renal_failure_syndrome": 40,
    "KAT2B-related_disorder": 21,
    "not_specified|KAT2B-related_disorder": 3,
    "KAT2B-related_disorder|not_provided": 1,
    "not_provided|KAT2B-related_disorder": 1,
    "SGO1-related_disorder|not_specified": 2,
    "Cardiovascular_phenotype|Chronic_atrial_and_intestinal_dysrhythmia": 1,
    "SGO1-related_disorder": 1,
    "SGO1-related_disorder|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|SGO1-related_disorder|Chronic_atrial_and_intestinal_dysrhythmia|not_provided": 1,
    "SGO1-related_disorder|not_provided": 1,
    "Normal_pregnancy|Small_for_gestational_age": 1,
    "not_provided|RPL15-related_disorder": 2,
    "Diamond-Blackfan_anemia_12": 11,
    "Diamond-Blackfan_anemia_12|not_specified|RPL15-related_disorder|not_provided": 1,
    "Diamond-Blackfan_anemia_12|not_provided|RPL15-related_disorder": 1,
    "not_provided|Diamond-Blackfan_anemia_12": 5,
    "RPL15-related_disorder|not_provided": 3,
    "not_provided|Diamond-Blackfan_anemia_12|RPL15-related_disorder": 1,
    "not_specified|not_provided|Diamond-Blackfan_anemia_12": 1,
    "RPL15-related_disorder": 6,
    "not_specified|RPL15-related_disorder|not_provided": 1,
    "not_provided|Diamond-Blackfan_anemia_12|not_specified": 1,
    "Familial_atrioventricular_septal_defect": 2,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided": 19,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 157,
    "Thyroid_hormone_resistance_syndrome": 26,
    "not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 8,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Resistance_to_thyroid_hormone_due_to_a_mutation_in_thyroid_hormone_receptor_beta|not_provided": 1,
    "Generalized_resistance_to_thyroid_hormone": 5,
    "THRB-related_disorder": 8,
    "not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_dominant|THRB-related_disorder": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|THRB-related_disorder|not_provided": 1,
    "not_specified|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 3,
    "THRB-related_disorder|Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_specified|not_provided": 4,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Neurodevelopmental_disorder|not_provided|THRB-related_disorder": 1,
    "Selective_pituitary_resistance_to_thyroid_hormone": 3,
    "Thyroid_hormone_resistance_syndrome|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "not_provided|THRB-related_disorder|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "not_specified|Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided": 1,
    "not_specified|THRB-related_disorder": 1,
    "not_provided|THRB-related_disorder": 2,
    "not_specified|not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Thyroid_hormone_resistance|_generalized|_autosomal_recessive": 1,
    "not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_recessive|Selective_pituitary_resistance_to_thyroid_hormone|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Inborn_genetic_diseases|THRB-related_disorder": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided|THRB-related_disorder|Selective_pituitary_resistance_to_thyroid_hormone|Thyroid_hormone_resistance|_generalized|_autosomal_recessive": 2,
    "not_provided|Thyroid_hormone_resistance_syndrome|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 2,
    "Selective_pituitary_resistance_to_thyroid_hormone|Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided": 1,
    "Generalized_resistance_to_thyroid_hormone|not_specified": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Thyroid_hormone_resistance|_generalized|_autosomal_recessive|not_provided|THRB-related_disorder|Thyroid_hormone_resistance_syndrome": 1,
    "not_provided|Selective_pituitary_resistance_to_thyroid_hormone|Thyroid_hormone_resistance|_generalized|_autosomal_recessive|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "not_provided|resistance_to_thyroid_hormone_(RTH)": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Selective_pituitary_resistance_to_thyroid_hormone": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided|not_specified": 1,
    "THRB-related_disorder|not_provided|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_specified": 2,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|not_provided|THRB-related_disorder": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Thyroid_hormone_resistance|_generalized|_autosomal_recessive|Selective_pituitary_resistance_to_thyroid_hormone|not_provided|THRB-related_disorder": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_dominant|Thyroid_hormone_resistance|_generalized|_autosomal_recessive|Selective_pituitary_resistance_to_thyroid_hormone": 1,
    "Thyroid_hormone_resistance|_generalized|_autosomal_recessive|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "not_provided|See_cases|Thyroid_hormone_resistance|_generalized|_autosomal_dominant": 1,
    "RARB-related_disorder|Intellectual_disability": 1,
    "RARB-related_disorder": 5,
    "Microphthalmia|_syndromic_12": 40,
    "Microphthalmia|_syndromic_12|not_provided": 3,
    "not_provided|RARB-related_disorder|Microphthalmia|_syndromic_12": 1,
    "not_provided|Microphthalmia|_syndromic_12": 4,
    "Intellectual_disability|_autosomal_dominant_48|Microphthalmia|_syndromic_12|not_provided": 1,
    "Microphthalmia|_syndromic_12|Inborn_genetic_diseases": 1,
    "not_provided|RARB-related_disorder": 1,
    "Microphthalmia|_syndromic_12|RARB-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_48": 21,
    "RARB-related_disorder|not_provided|Microphthalmia|_syndromic_12": 1,
    "Intellectual_disability|_autosomal_dominant_48|Inborn_genetic_diseases|Microphthalmia|_syndromic_12|not_provided": 1,
    "Inborn_genetic_diseases|Microphthalmia|_syndromic_12": 1,
    "RARB-related_disorder|Microphthalmia|_syndromic_12": 1,
    "TOP2B-related_neurodevelopmental_disorder|not_provided": 1,
    "TOP2B-related_disorder|not_provided|not_specified": 2,
    "B-cell_immunodeficiency|_distal_limb_anomalies|_and_urogenital_malformations|not_provided": 4,
    "TOP2B-related_disorder|not_provided": 7,
    "not_provided|TOP2B-related_disorder": 10,
    "TOP2B-related_disorder": 3,
    "B-cell_immunodeficiency|_distal_limb_anomalies|_and_urogenital_malformations": 11,
    "not_provided|B-cell_immunodeficiency|_distal_limb_anomalies|_and_urogenital_malformations": 2,
    "not_provided|not_specified|B-cell_immunodeficiency|_distal_limb_anomalies|_and_urogenital_malformations": 1,
    "TOP2B-related_disorder|not_specified|not_provided": 2,
    "not_provided|TOP2B-related_disorder|not_specified": 1,
    "Congenital_disorder_of_deglycosylation|not_provided": 27,
    "Congenital_disorder_of_deglycosylation": 608,
    "Congenital_disorder_of_deglycosylation_1|Congenital_disorder_of_deglycosylation": 5,
    "Congenital_disorder_of_deglycosylation_1": 18,
    "Congenital_disorder_of_deglycosylation|not_provided|Inborn_genetic_diseases": 4,
    "Congenital_disorder_of_deglycosylation_1|Congenital_disorder_of_deglycosylation|not_provided": 3,
    "Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation": 17,
    "not_provided|Congenital_disorder_of_deglycosylation": 22,
    "Congenital_disorder_of_deglycosylation|Inborn_genetic_diseases": 17,
    "not_specified|Congenital_disorder_of_deglycosylation": 6,
    "Congenital_disorder_of_deglycosylation|Congenital_disorder_of_deglycosylation_1": 6,
    "Congenital_disorder_of_deglycosylation|Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation_1": 1,
    "not_provided|Congenital_disorder_of_deglycosylation_1|Congenital_disorder_of_deglycosylation": 2,
    "not_provided|NGLY1-related_disorder|Congenital_disorder_of_deglycosylation": 3,
    "not_provided|Congenital_disorder_of_deglycosylation_1|Congenital_disorder_of_deglycosylation|Intellectual_disability|Neuromotor_delay|Peripheral_neuropathy": 1,
    "not_specified|NGLY1-related_disorder|Congenital_disorder_of_deglycosylation": 2,
    "Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation|not_provided": 2,
    "Congenital_disorder_of_deglycosylation_1|Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation|not_provided": 1,
    "Congenital_disorder_of_deglycosylation|NGLY1-related_disorder": 3,
    "NGLY1-related_disorder|Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation|not_provided": 1,
    "Congenital_disorder_of_deglycosylation|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Congenital_disorder_of_deglycosylation": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation": 3,
    "Inborn_genetic_diseases|Congenital_disorder_of_deglycosylation|Congenital_disorder_of_deglycosylation_1|not_provided": 1,
    "Congenital_disorder_of_deglycosylation_1|not_provided|Congenital_disorder_of_deglycosylation": 2,
    "Congenital_disorder_of_deglycosylation|not_specified": 3,
    "Congenital_disorder_of_deglycosylation_1|Neurodevelopmental_abnormality": 1,
    "Congenital_disorder_of_deglycosylation|Congenital_disorder_of_deglycosylation_1|Intellectual_disability|not_provided": 1,
    "not_provided|Neurodevelopmental_delay|Congenital_disorder_of_deglycosylation": 1,
    "Congenital_disorder_of_deglycosylation|Congenital_disorder_of_deglycosylation_1|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Congenital_disorder_of_deglycosylation|Inborn_genetic_diseases": 1,
    "not_specified|Global_developmental_delay|Fetal_growth_restriction|Lactic_acidosis": 1,
    "NGLY1-related_disorder|Congenital_disorder_of_deglycosylation": 2,
    "Congenital_disorder_of_deglycosylation|not_provided|NGLY1-related_disorder": 1,
    "NGLY1-related_disorder|not_provided|Congenital_disorder_of_deglycosylation": 1,
    "not_provided|Congenital_disorder_of_deglycosylation|Inborn_genetic_diseases": 2,
    "Congenital_disorder_of_deglycosylation|NGLY1-related_disorder|not_provided": 1,
    "Congenital_disorder_of_deglycosylation|Congenital_disorder_of_deglycosylation_1|not_provided": 1,
    "not_provided|Congenital_disorder_of_deglycosylation|not_specified": 1,
    "Congenital_disorder_of_deglycosylation|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_disorder_of_deglycosylation|not_provided|Congenital_disorder_of_deglycosylation_1|Inborn_genetic_diseases": 1,
    "Congenital_disorder_of_deglycosylation|not_provided|Congenital_disorder_of_deglycosylation_1": 1,
    "not_specified|Congenital_disorder_of_deglycosylation_1|Congenital_disorder_of_deglycosylation": 1,
    "not_specified|Ciliary_dyskinesia|_primary|_44": 1,
    "Ciliary_dyskinesia|_primary|_44|not_provided": 9,
    "Ciliary_dyskinesia|_primary|_44": 8,
    "NEK10-related_disorder": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_44": 1,
    "SLC4A7-related_disorder": 9,
    "not_provided|EOMES-related_disorder": 2,
    "EOMES-related_disorder": 6,
    "Microcephaly-polymicrogyria-corpus_callosum_agenesis_syndrome|not_specified|not_provided": 1,
    "EOMES-related_disorder|not_provided": 2,
    "Diabetic_retinopathy|Loeys-Dietz_syndrome_2": 3,
    "Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Marfan_syndrome|Diabetic_retinopathy|Loeys-Dietz_syndrome": 1,
    "Marfan_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Diabetic_retinopathy": 6,
    "Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Marfan_syndrome|Diabetic_retinopathy|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Diabetic_retinopathy|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome_2": 325,
    "Diabetic_retinopathy|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Marfan_syndrome|Loeys-Dietz_syndrome": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|not_provided|Loeys-Dietz_syndrome": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Marfan_syndrome": 1,
    "TGFBR2-related_disorder": 4,
    "Diabetic_retinopathy|not_provided": 2,
    "not_specified|Diabetic_retinopathy": 3,
    "not_provided|Diabetic_retinopathy": 4,
    "Diabetic_retinopathy|Marfan_syndrome|Loeys-Dietz_syndrome_2|not_provided|Loeys-Dietz_syndrome": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 13,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Diabetic_retinopathy": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 66,
    "Diabetic_retinopathy|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "TGFBR2-related_disorder|Diabetic_retinopathy|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|not_provided": 16,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Diabetic_retinopathy": 4,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy": 1,
    "Loeys-Dietz_syndrome_2|not_provided|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR2-related_disorder|not_provided|Loeys-Dietz_syndrome_2|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Diabetic_retinopathy|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|Diabetic_retinopathy|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 41,
    "Loeys-Dietz_syndrome_2|Diabetic_retinopathy|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy|Loeys-Dietz_syndrome_2|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|not_provided": 12,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy|not_provided": 1,
    "Diabetic_retinopathy|not_provided|not_specified": 1,
    "not_specified|Diabetic_retinopathy|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|TGFBR2-related_disorder|Diabetic_retinopathy|not_provided": 1,
    "Diabetic_retinopathy|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR2-related_disorder|Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Diabetic_retinopathy": 1,
    "Isolated_thoracic_aortic_aneurysm|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|not_specified|not_provided|TGFBR2-related_disorder|Diabetic_retinopathy": 1,
    "Loeys-Dietz_syndrome_2|not_specified|Diabetic_retinopathy|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Diabetic_retinopathy|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy|Loeys-Dietz_syndrome_2": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Diabetic_retinopathy": 1,
    "Thoracic_aortic_aneurysm|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|Marfan_syndrome|not_provided": 1,
    "Diabetic_retinopathy|not_specified": 1,
    "Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_provided|Diabetic_retinopathy|not_specified": 1,
    "Loeys-Dietz_syndrome_2|Diabetic_retinopathy|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "TGFBR2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Diabetic_retinopathy|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome_2|Diabetic_retinopathy|not_provided": 1,
    "Diabetic_retinopathy|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Diabetic_retinopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR2-related_disorder|Loeys-Dietz_syndrome_2": 2,
    "Diabetic_retinopathy|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Congenital_aneurysm_of_ascending_aorta|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Diabetic_retinopathy|not_specified": 1,
    "Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 3,
    "TGFBR2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Ehlers-Danlos_syndrome|not_provided": 1,
    "not_provided|Thoracic_aortic_aneurysm|not_specified|Cardiovascular_phenotype|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 3,
    "Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|not_specified|TGFBR2-related_disorder": 1,
    "Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|not_provided": 1,
    "Loeys-Dietz_syndrome_2|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|not_specified": 1,
    "Loeys-Dietz_syndrome_2|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "TGFBR2-related_disorder|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_provided|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR2-related_disorder|not_provided|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome_2|TGFBR2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "Marfan_syndrome|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome": 1,
    "TGFBR2-related_disorder|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus": 2,
    "Cardiovascular_phenotype|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 93,
    "not_provided|Cardiovascular_phenotype|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 2,
    "not_provided|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome_2|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 4,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|Familial_colorectal_cancer": 1,
    "Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_provided": 1,
    "Loeys-Dietz_syndrome_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome|Loeys-Dietz_syndrome|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome_2|TGFBR2-related_disorder|not_specified": 1,
    "TGFBR2-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome_1": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Loeys-Dietz_syndrome_2|not_provided|Marfan_syndrome": 1,
    "not_specified|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Loeys-Dietz_syndrome|Lynch_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|TGFBR2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|TGFBR2-related_disorder": 1,
    "Marfan_syndrome|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 52,
    "Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2": 1,
    "not_provided|Loeys-Dietz_syndrome_2|TGFBR2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR2-related_disorder|not_specified|Loeys-Dietz_syndrome_2|not_provided": 1,
    "not_provided|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_provided|Loeys-Dietz_syndrome_2|TGFBR2-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|not_provided|Cardiovascular_phenotype": 1,
    "Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Cardiovascular_phenotype": 1,
    "Thoracic_aortic_aneurysm|Loeys-Dietz_syndrome|Thoracic_aortic_dissection|TGFBR2-related_disorder|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Marfan_syndrome": 1,
    "Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR2-related_disorder|not_specified|Ehlers-Danlos_syndrome|Ascending_tubular_aorta_aneurysm|Vascular_dilatation": 1,
    "Loeys-Dietz_syndrome_2|not_provided|Thoracic_aortic_aneurysm|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Cardiovascular_phenotype|Loeys-Dietz_syndrome": 1,
    "Isolated_thoracic_aortic_aneurysm|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR2-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR2-related_disorder": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2": 1,
    "Multiple_congenital_anomalies/dysmorphic_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome_1|TGFBR2-related_disorder": 1,
    "Malignant_tumor_of_esophagus|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "not_provided|Loeys-Dietz_syndrome_2": 16,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2": 1,
    "Malignant_tumor_of_esophagus": 5,
    "Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Malignant_tumor_of_esophagus|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus": 1,
    "Loeys-Dietz_syndrome_2|Cardiovascular_phenotype|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6": 1,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Loeys-Dietz_syndrome_2|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Thoracic_aortic_aneurysm_or_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1": 6,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 2,
    "Loeys-Dietz_syndrome_2|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_specified|not_provided|TGFBR2-related_disorder|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Isolated_thoracic_aortic_aneurysm|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6": 1,
    "Loeys-Dietz_syndrome_2|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus": 1,
    "Wolff-Parkinson-White_pattern|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Loeys-Dietz_syndrome_2": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_specified|not_provided": 1,
    "TGFBR2-related_disorder|Cardiovascular_phenotype|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_provided": 1,
    "TGFBR2-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_6": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6": 1,
    "Malignant_tumor_of_esophagus|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR2-related_disorder|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome|Congenital_aneurysm_of_ascending_aorta|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|TGFBR2-related_disorder|not_provided": 1,
    "Marfan_syndrome|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome": 2,
    "Loeys-Dietz_syndrome_2|Marfan_syndrome|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome_2|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 8,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome|Marfan_syndrome": 1,
    "Marfan_syndrome|Malignant_tumor_of_esophagus|Loeys-Dietz_syndrome_2|Colorectal_cancer|_hereditary_nonpolyposis|_type_6|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Loeys-Dietz_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Marfan_syndrome": 4,
    "not_provided|Marfan_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome": 5,
    "Marfan_syndrome|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2": 1,
    "Marfan_syndrome|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|Loeys-Dietz_syndrome": 1,
    "Marfan_syndrome|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_2|not_provided|Marfan_syndrome": 1,
    "Loeys-Dietz_syndrome|Marfan_syndrome|Loeys-Dietz_syndrome_2": 2,
    "Loeys-Dietz_syndrome_2|not_provided|Marfan_syndrome|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome|not_provided|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Loeys-Dietz_syndrome|Marfan_syndrome|Loeys-Dietz_syndrome_2": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_2|Marfan_syndrome": 1,
    "STT3B-related_disorder": 1,
    "STT3B-congenital_disorder_of_glycosylation": 68,
    "not_specified|STT3B-congenital_disorder_of_glycosylation|not_provided": 2,
    "STT3B-congenital_disorder_of_glycosylation|not_specified|not_provided": 2,
    "STT3B-congenital_disorder_of_glycosylation|not_specified": 6,
    "STT3B-related_disorder|STT3B-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_provided|STT3B-congenital_disorder_of_glycosylation|not_specified": 1,
    "not_provided|not_specified|STT3B-congenital_disorder_of_glycosylation": 2,
    "not_specified|not_provided|STT3B-congenital_disorder_of_glycosylation": 2,
    "not_specified|STT3B-congenital_disorder_of_glycosylation": 3,
    "STT3B-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|STT3B-congenital_disorder_of_glycosylation": 2,
    "STT3B-related_disorder|not_specified|STT3B-congenital_disorder_of_glycosylation": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_provided": 32,
    "Cardiovascular_phenotype|Brugada_syndrome": 351,
    "Brugada_syndrome|Cardiovascular_phenotype": 318,
    "Brugada_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype|Brugada_syndrome_2": 1,
    "not_provided|Brugada_syndrome": 41,
    "Brugada_syndrome|Brugada_syndrome_2|Cardiovascular_phenotype": 4,
    "not_specified|Brugada_syndrome": 105,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Brugada_syndrome_2": 3,
    "not_provided|Brugada_syndrome|Brugada_syndrome_2": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|not_specified": 7,
    "Brugada_syndrome|not_specified": 92,
    "Brugada_syndrome_2|not_provided": 1,
    "Brugada_syndrome|Brugada_syndrome_2": 1,
    "Brugada_syndrome_2|not_provided|GPD1L-related_disorder": 1,
    "GPD1L-related_disorder|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Long_QT_syndrome|not_specified|not_provided|Brugada_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Hypertrophic_cardiomyopathy|Brugada_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome": 47,
    "Cardiovascular_phenotype|Brugada_syndrome|Brugada_syndrome_2": 3,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome": 2,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype": 30,
    "Cardiovascular_phenotype|Brugada_syndrome|not_specified": 9,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome": 27,
    "GPD1L-related_disorder|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_2|not_provided": 1,
    "Brugada_syndrome_2|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "not_provided|Brugada_syndrome_2|Cardiovascular_phenotype|not_specified|Brugada_syndrome": 1,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype": 6,
    "Brugada_syndrome_2|Brugada_syndrome": 2,
    "Cardiovascular_phenotype|Brugada_syndrome|not_provided|Brugada_syndrome_2": 1,
    "Brugada_syndrome_2|not_specified|Brugada_syndrome|Sudden_cardiac_death|Cardiovascular_phenotype|not_provided": 1,
    "Brugada_syndrome_2|not_specified|not_provided|Brugada_syndrome|GPD1L-related_disorder": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|GPD1L-related_disorder": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_2|not_provided|Brugada_syndrome": 1,
    "not_provided|Cardiomyopathy|not_specified|GPD1L-related_disorder|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Long_QT_syndrome": 1,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype": 38,
    "Brugada_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Primary_dilated_cardiomyopathy|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_2|Wolff-Parkinson-White_pattern|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype|Brugada_syndrome_2": 1,
    "Cardiovascular_phenotype|GPD1L-related_disorder|Brugada_syndrome": 1,
    "GPD1L-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|Brugada_syndrome_2|Death_in_infancy": 1,
    "not_specified|not_provided|Brugada_syndrome": 7,
    "Brugada_syndrome|Cardiovascular_phenotype|Brugada_syndrome_2": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome|not_specified": 3,
    "Brugada_syndrome_2|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|not_provided": 24,
    "Brugada_syndrome_2": 1,
    "Brugada_syndrome_2|not_specified|Brugada_syndrome": 1,
    "Brugada_syndrome_2|not_specified|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Brugada_syndrome_2|Brugada_syndrome|GPD1L-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Brugada_syndrome": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_2|Brugada_syndrome": 1,
    "Brugada_syndrome_2|Cardiovascular_phenotype|not_specified|Brugada_syndrome": 1,
    "TRIM71-related_disorder": 10,
    "Hydrocephalus|_congenital_communicating|_1|not_specified": 1,
    "Hydrocephalus|_congenital_communicating|_1": 10,
    "Cryptozoospermia": 4,
    "not_specified|Hydrocephalus|_congenital_communicating|_1": 1,
    "Hydrocephalus|_congenital_communicating|_1|not_provided|Non-obstructive_azoospermia": 1,
    "not_provided|TRIM71-related_disorder": 1,
    "TRIM71-related_disorder|not_provided": 1,
    "Non-obstructive_azoospermia|not_provided": 4,
    "Non-obstructive_azoospermia|Hydrocephalus|_congenital_communicating|_1|not_provided": 1,
    "Congenital_hydrocephalus": 6,
    "Hydrocephalus|_congenital_communicating|_1|Congenital_hydrocephalus|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 475,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 10,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided": 7,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 223,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 21,
    "GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis": 2,
    "Infantile_GM1_gangliosidosis": 29,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_specified": 4,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B": 7,
    "GM1_gangliosidosis_type_2|GLB1-related_disorder|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|not_provided|GM1_gangliosidosis": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided": 6,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis": 5,
    "Inborn_genetic_diseases|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Inborn_genetic_diseases": 4,
    "GM1_gangliosidosis": 7,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GLB1-related_disorder|not_provided": 2,
    "not_specified|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided|Infantile_GM1_gangliosidosis": 2,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 2,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis": 2,
    "Inborn_genetic_diseases|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Inborn_genetic_diseases|not_specified|See_cases": 1,
    "GM1_gangliosidosis_type_2|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1-gangliosidosis|_type_I|_with_cardiac_involvement": 1,
    "GM1-gangliosidosis|_type_I|_with_cardiac_involvement": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Progressive_familial_intrahepatic_cholestasis|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided|Infantile_GM1_gangliosidosis|GLB1-related_disorder": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 3,
    "not_provided|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis": 2,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Morquio_syndrome": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|not_provided|Inborn_genetic_diseases|GM1_gangliosidosis": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis": 8,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "not_provided|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Inborn_genetic_diseases": 7,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2": 4,
    "Morquio_syndrome|GM1_gangliosidosis": 2,
    "GLB1-related_disorder|not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|not_specified": 1,
    "GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|Inborn_genetic_diseases|GLB1-related_disorder|not_provided": 1,
    "GLB1-related_disorder": 5,
    "GLB1-related_disorder|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|not_provided": 1,
    "Intellectual_disability|not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|Inborn_genetic_diseases|GM1_gangliosidosis": 1,
    "Inborn_genetic_diseases|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 3,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_specified": 3,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided|not_specified": 1,
    "not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 7,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 4,
    "Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|GM1_gangliosidosis|GLB1-related_disorder": 2,
    "Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3": 2,
    "not_provided|GM1_gangliosidosis_type_3|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|not_provided|GM1_gangliosidosis|GM1-gangliosidosis|_type_I|_with_cardiac_involvement": 1,
    "Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 3,
    "GM1_gangliosidosis|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis": 3,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_provided": 4,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|GM1_gangliosidosis": 5,
    "not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|not_provided": 1,
    "GLB1-related_disorder|not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3": 3,
    "GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "GM1_gangliosidosis|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GLB1-related_disorder": 3,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|GM1_gangliosidosis|GLB1-related_disorder|not_provided": 1,
    "GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis|not_provided": 1,
    "Spondyloepiphyseal_dysplasia|GM1_gangliosidosis|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|not_provided": 1,
    "GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3": 3,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|not_provided|GM1_gangliosidosis": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|GLB1-related_disorder|not_specified": 1,
    "GLB1-related_disorder|not_specified|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis": 1,
    "not_specified|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 6,
    "Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis": 2,
    "GLB1-related_disorder|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis": 1,
    "GM1_gangliosidosis_type_2": 6,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3": 2,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2": 4,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided|Infantile_GM1_gangliosidosis": 1,
    "not_specified|not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Spastic_ataxia|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis|not_provided|GM1-gangliosidosis|_type_I|_with_cardiac_involvement": 1,
    "GM1_gangliosidosis|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis_type_3": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis": 3,
    "GM1_gangliosidosis|not_provided|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 2,
    "Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis": 2,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided|Inborn_genetic_diseases": 2,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "GLB1-related_disorder|not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Infantile_GM1_gangliosidosis|Inborn_genetic_diseases": 1,
    "GM1_gangliosidosis_type_3|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "Intellectual_disability|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|not_specified|not_provided|GM1_gangliosidosis": 1,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis": 1,
    "GLB1-related_disorder|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis": 1,
    "GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 2,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|not_provided|GM1_gangliosidosis": 1,
    "not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_specified": 1,
    "GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_provided|Inborn_genetic_diseases|GLB1-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided|Infantile_GM1_gangliosidosis|not_specified": 1,
    "GLB1-related_disorder|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 2,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_specified|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|not_specified|GM1_gangliosidosis|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|not_provided|Infantile_GM1_gangliosidosis": 2,
    "not_provided|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 3,
    "Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis_type_2|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|not_provided": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3": 1,
    "Mucopolysaccharidosis|_MPS-IV-B": 5,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_provided|Inborn_genetic_diseases|GM1_gangliosidosis_type_2": 1,
    "GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided": 1,
    "GLB1-related_disorder|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis|not_specified": 1,
    "Infantile_GM1_gangliosidosis|GLB1-related_disorder|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|not_provided": 1,
    "not_specified|Infantile_GM1_gangliosidosis|not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|not_provided": 1,
    "not_provided|GLB1-related_disorder|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "GLB1-related_disorder|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_specified|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_specified|not_provided": 1,
    "GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|Inborn_genetic_diseases": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_3": 1,
    "GM1_gangliosidosis_type_3|not_provided|Inborn_genetic_diseases|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_3|not_provided": 1,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "not_provided|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3": 1,
    "GM1_gangliosidosis_type_3|GM1_gangliosidosis_type_2|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_specified|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3": 1,
    "GLB1-related_disorder|Inborn_genetic_diseases|GM1_gangliosidosis|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|not_provided|GM1-gangliosidosis|_type_I|_with_cardiac_involvement": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3": 1,
    "GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|GM1_gangliosidosis|not_provided": 1,
    "GM1_gangliosidosis_type_3|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis": 1,
    "GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|Infantile_GM1_gangliosidosis|GM1_gangliosidosis": 1,
    "Inborn_genetic_diseases|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis|not_provided": 1,
    "Infantile_GM1_gangliosidosis|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|not_provided": 1,
    "not_provided|GLB1-related_disorder": 2,
    "GLB1-related_disorder|not_provided": 1,
    "not_specified|GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|not_provided": 1,
    "Inborn_genetic_diseases|GM1_gangliosidosis_type_3|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|Infantile_GM1_gangliosidosis|not_provided|GM1_gangliosidosis": 1,
    "GM1_gangliosidosis|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3|Infantile_GM1_gangliosidosis|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis": 1,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|Infantile_GM1_gangliosidosis|not_specified|not_provided|GM1_gangliosidosis_type_2|GM1_gangliosidosis_type_3": 2,
    "Mucopolysaccharidosis|_MPS-IV-B|GM1_gangliosidosis|GLB1-related_disorder|not_provided|Infantile_GM1_gangliosidosis|not_specified": 1,
    "GM1_gangliosidosis|Morquio_syndrome": 1,
    "Osteogenesis_imperfecta_type_7": 496,
    "Osteogenesis_imperfecta_type_7|not_provided": 19,
    "not_specified|Osteogenesis_imperfecta_type_7": 4,
    "Osteogenesis_imperfecta_type_7|Osteogenesis_imperfecta": 5,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta_type_7": 13,
    "CRTAP-related_disorder|Osteogenesis_imperfecta_type_7": 5,
    "Osteogenesis_imperfecta_type_7|Inborn_genetic_diseases": 13,
    "not_provided|Osteogenesis_imperfecta_type_7": 17,
    "Osteogenesis_imperfecta_type_7|not_specified": 5,
    "not_provided|Osteogenesis_imperfecta_type_7|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_7": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_7": 2,
    "CRTAP-related_disorder": 2,
    "Osteogenesis_imperfecta_type_7|CRTAP-related_disorder": 3,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_7": 1,
    "not_specified|Osteogenesis_imperfecta_type_7|not_provided|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_7": 2,
    "Osteogenesis_imperfecta|CRTAP-related_disorder|Osteogenesis_imperfecta_type_7": 1,
    "not_specified|Osteogenesis_imperfecta_type_7|CRTAP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_7": 1,
    "Osteogenesis_imperfecta_type_7|not_provided|Osteogenesis_imperfecta": 1,
    "CRTAP-related_disorder|Osteogenesis_imperfecta_type_7|Inborn_genetic_diseases": 1,
    "not_provided|Osteogenesis_imperfecta_type_7|CRTAP-related_disorder|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_7|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta|not_specified|Osteogenesis_imperfecta_type_7|not_provided": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta_type_7|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_7|not_specified|not_provided": 1,
    "Osteogenesis_imperfecta|not_provided|not_specified|Osteogenesis_imperfecta_type_7": 1,
    "not_provided|Osteogenesis_imperfecta_type_7|not_specified": 2,
    "Osteogenesis_imperfecta_type_7|CRTAP-related_disorder|Osteogenesis_imperfecta": 1,
    "CRTAP-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_7": 1,
    "not_specified|Osteogenesis_imperfecta_type_7|not_provided": 1,
    "Osteogenesis_imperfecta_type_7|not_specified|CRTAP-related_disorder|not_provided|Osteogenesis_imperfecta": 1,
    "CLASP2-related_disorder": 18,
    "not_provided|CLASP2-related_disorder": 3,
    "CLASP2-related_disorder|not_provided": 1,
    "Microcephaly_29|_primary|_autosomal_recessive": 1,
    "Monomelic_amyotrophy": 2,
    "MLH1-related_disorder": 8,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 22,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 346,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Familial_cancer_of_breast": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_colorectal_cancer": 1,
    "not_provided|MLH1-related_disorder": 1,
    "MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 20,
    "Lynch_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Inherited_MMR_deficiency_(Lynch_syndrome)|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome_1": 1,
    "Colonic_neoplasm|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 3,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 2,
    "Lynch_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 4,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 44,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 85,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 7,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 70,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 51,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 52,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 10,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 6,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 60,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 45,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 10,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 3,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 111,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 6,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 4,
    "Lynch_syndrome_1|Malignant_tumor_of_breast|Lynch_syndrome|Breast_and/or_ovarian_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Malignant_tumor_of_breast|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 44,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 4,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1": 4,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 22,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 18,
    "Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 13,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 55,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lung_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified": 2,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome|not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 7,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 2,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 5,
    "not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 5,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch-like_syndrome|not_provided|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 14,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 2,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Gastric_cancer": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 8,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 8,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|See_cases|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon": 3,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Muir-Torr\u00e9_syndrome": 1,
    "Gastric_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 5,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Carcinoma_of_colon|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1|Colon_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified": 5,
    "Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Muir-Torr\u00e9_syndrome": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 5,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 3,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 4,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Colorectal_cancer|_sporadic|_susceptibility_to|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 4,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Lynch_syndrome|not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Muir-Torr\u00e9_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Lynch_syndrome|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 8,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer|MLH1-related_disorder": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Inherited_MMR_deficiency_(Lynch_syndrome)": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1|Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|not_provided|Malignant_tumor_of_breast|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_specified|not_provided|Breast_and/or_ovarian_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 9,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_specified": 1,
    "Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch-like_syndrome|Gastric_cancer|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|MLH1-related_disorder|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_1|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Lynch-like_syndrome|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Colonic_neoplasm|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 4,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colon_cancer|Carcinoma_of_colon|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Colorectal_cancer|_non-polyposis|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Colon_cancer|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 7,
    "Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MLH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MLH1-related_disorder": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|See_cases": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "MLH1-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 2,
    "MLH1-related_disorder|Hereditary_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 3,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Colorectal_cancer|_non-polyposis|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 2,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_non-polyposis|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified": 1,
    "Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_1|Breast_and/or_ovarian_cancer|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_carcinoma|Lynch_syndrome|not_specified|MLH1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer|not_specified|Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|not_specified|not_provided|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Ovarian_cancer|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Bile_duct_cancer|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer|Childhood_neoplasm|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|not_specified": 1,
    "not_provided|Colon_cancer": 1,
    "Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Breast_and/or_ovarian_cancer|not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 5,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 2,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_provided|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Familial_cancer_of_breast|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome|Muir-Torr\u00e9_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Muir-Torr\u00e9_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Muir-Torr\u00e9_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Primary_peritoneal_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_ovarian_cancer_(without_breast_cancer)|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch-like_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Familial_cancer_of_breast|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Colon_cancer|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Familial_cancer_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Familial_colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Lynch_syndrome|not_specified": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder|not_specified|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|not_specified|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "not_provided|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Malignant_tumor_of_breast|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|MLH1-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Familial_colorectal_cancer|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Lynch-like_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_non-polyposis|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|MLH1-related_disorder|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "MLH1-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome|MLH1-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_breast_ovarian_cancer_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Lynch_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Endometrial_carcinoma": 1,
    "not_provided|MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Colorectal_cancer|_non-polyposis|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|not_provided|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch-like_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|MLH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Muir-Torr\u00e9_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Hereditary_nonpolyposis_colon_cancer|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Lynch_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|MLH1-related_disorder|Muir-Torr\u00e9_syndrome": 1,
    "Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|MLH1-related_disorder|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Lynch_syndrome": 1,
    "Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch-like_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1": 1,
    "Breast_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colon_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|not_specified": 1,
    "MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Lynch_syndrome": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome_1|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "MLH1-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "not_provided|Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|MLH1-related_disorder": 1,
    "Muir-Torr\u00e9_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_specified|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|MLH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Muir-Torr\u00e9_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Lynch_syndrome_1": 1,
    "MLH1-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Mismatch_repair_cancer_syndrome_1|Muir-Torr\u00e9_syndrome|Lynch_syndrome|not_specified": 1,
    "Muir-Torr\u00e9_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_2|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_2|not_provided|not_specified": 1,
    "GOLGA4-related_disorder": 6,
    "APRG1-related_disorder": 1,
    "not_provided|ITGA9-related_disorder": 3,
    "ITGA9-related_disorder": 20,
    "ITGA9-related_disorder|not_specified|not_provided": 1,
    "not_specified|ITGA9-related_disorder|not_provided": 1,
    "ITGA9-related_disorder|not_provided": 1,
    "Preeclampsia|Gestational_diabetes_mellitus_uncontrolled|Normal_pregnancy": 1,
    "VILL-related_disorder": 2,
    "not_provided|PLCD1-related_disorder": 5,
    "Nonsyndromic_congenital_nail_disorder_3": 8,
    "not_specified|PLCD1-related_disorder": 1,
    "PLCD1-related_disorder|Nonsyndromic_congenital_nail_disorder_3": 1,
    "PLCD1-related_disorder": 13,
    "not_provided|Nonsyndromic_congenital_nail_disorder_3": 1,
    "Nonsyndromic_congenital_nail_disorder_3|not_specified": 1,
    "Primary_degenerative_dementia_of_the_Alzheimer_type|_presenile_onset": 3,
    "not_specified|Nonsyndromic_congenital_nail_disorder_3": 2,
    "PLCD1-related_disorder|not_provided": 2,
    "ACAA1-related_disorder": 7,
    "ACAA1-related_disorder|not_provided": 1,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency": 128,
    "MYD88-related_disorder|Pyogenic_bacterial_infections_due_to_MyD88_deficiency": 1,
    "not_provided|not_specified|Pyogenic_bacterial_infections_due_to_MyD88_deficiency|Inborn_genetic_diseases": 1,
    "MYD88-related_disorder": 1,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency|MYD88-related_disorder|not_provided": 1,
    "MYD88-related_disorder|not_specified|Pyogenic_bacterial_infections_due_to_MyD88_deficiency": 1,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency|not_provided": 2,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency|Inborn_genetic_diseases": 5,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency|not_specified": 1,
    "not_provided|Pyogenic_bacterial_infections_due_to_MyD88_deficiency": 2,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency|MYD88-related_disorder": 1,
    "Inborn_genetic_diseases|Pyogenic_bacterial_infections_due_to_MyD88_deficiency": 3,
    "Pyogenic_bacterial_infections_due_to_MyD88_deficiency|Malignant_lymphoma|_large_B-cell|_diffuse|Macroglobulinemia|_Waldenstrom|_somatic": 1,
    "Heterotaxy|_visceral|_4|_autosomal": 254,
    "not_provided|Heterotaxy|_visceral|_4|_autosomal": 28,
    "not_specified|Heterotaxy|_visceral|_4|_autosomal": 7,
    "ACVR2B-related_disorder": 6,
    "not_specified|not_provided|Heterotaxy|_visceral|_4|_autosomal": 2,
    "Heterotaxy|_visceral|_4|_autosomal|ACVR2B-related_disorder": 2,
    "Heterotaxy|_visceral|_4|_autosomal|not_specified|not_provided": 1,
    "Heterotaxy|_visceral|_4|_autosomal|not_specified": 4,
    "ACVR2B-related_disorder|Heterotaxy|_visceral|_4|_autosomal": 2,
    "not_provided|Heterotaxy|_visceral|_4|_autosomal|not_specified": 3,
    "Heterotaxy|_visceral|_4|_autosomal|not_provided": 3,
    "not_specified|Heterotaxy|_visceral|_4|_autosomal|not_provided": 1,
    "Heterotaxy|_visceral|_4|_autosomal|not_provided|not_specified": 2,
    "not_provided|Visceral_heterotaxy": 3,
    "Visceral_heterotaxy|not_provided": 4,
    "Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Brugada_syndrome|Long_QT_syndrome|Progressive_familial_heart_block": 3,
    "Paroxysmal_familial_ventricular_fibrillation|Progressive_familial_heart_block|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Brugada_syndrome|Long_QT_syndrome": 2,
    "Brugada_syndrome_1|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 4,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 5,
    "Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3": 13,
    "Paroxysmal_familial_ventricular_fibrillation|Progressive_familial_heart_block|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Brugada_syndrome": 2,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3": 2,
    "Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Brugada_syndrome|Long_QT_syndrome|Paroxysmal_familial_ventricular_fibrillation|Progressive_familial_heart_block": 1,
    "Brugada_syndrome|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Paroxysmal_familial_ventricular_fibrillation|Progressive_familial_heart_block": 3,
    "Brugada_syndrome|Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Progressive_familial_heart_block": 3,
    "Dilated_Cardiomyopathy|_Dominant|Paroxysmal_familial_ventricular_fibrillation|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Brugada_syndrome|Long_QT_syndrome|Progressive_familial_heart_block": 2,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 2,
    "Brugada_syndrome_1|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E": 1,
    "not_provided|Brugada_syndrome|Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Progressive_familial_heart_block": 1,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 4,
    "Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3": 5,
    "Progressive_familial_heart_block|_type_1A|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|not_provided|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 1,
    "Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|not_provided": 1,
    "Congenital_long_QT_syndrome|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 2,
    "Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 2,
    "Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Dilated_cardiomyopathy_1E": 3,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|not_provided|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Congenital_long_QT_syndrome|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|not_provided|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome|Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Long_QT_syndrome|Progressive_familial_heart_block|Congenital_long_QT_syndrome": 4,
    "Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|not_provided|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome_1|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3": 1,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|not_provided|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1": 2,
    "Congenital_long_QT_syndrome|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|not_provided|Dilated_cardiomyopathy_1E": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3": 1,
    "Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Long_QT_syndrome|Progressive_familial_heart_block|Brugada_syndrome|Congenital_long_QT_syndrome": 1,
    "Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Progressive_familial_heart_block|Brugada_syndrome": 1,
    "not_provided|Cardiac_arrhythmia": 184,
    "not_provided|Cardiac_arrhythmia|not_specified": 3,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 60,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 1,
    "Cardiac_arrhythmia|not_specified": 19,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|Long_QT_syndrome_3|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 87,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia": 20,
    "not_provided|Long_QT_syndrome_3|Cardiac_arrhythmia|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Congenital_long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified": 9,
    "Cardiac_arrhythmia|not_provided": 192,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided": 11,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 26,
    "Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Cardiac_arrhythmia": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Brugada_syndrome_1|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3": 1,
    "Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1|not_specified|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome|Brugada_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiomyopathy": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_specified|Brugada_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|not_specified": 5,
    "SCN5A-related_disorder": 11,
    "Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|not_specified|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|SCN5A-related_disorder|Long_QT_syndrome_3|not_specified|Congenital_long_QT_syndrome|Cardiomyopathy": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1|Brugada_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Long_QT_syndrome_3|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia": 21,
    "Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype": 2,
    "Brugada_syndrome_1": 39,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiac_arrhythmia|Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Progressive_familial_heart_block|_type_1A|SCN5A-related_disorder|not_specified|not_provided|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|not_specified|not_provided|Atrial_fibrillation|_familial|_10": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Progressive_familial_heart_block|Brugada_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome": 2,
    "not_provided|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1": 1,
    "not_provided|Congenital_long_QT_syndrome": 28,
    "Cardiac_arrhythmia|Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME": 2,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 2,
    "Cardiac_arrhythmia|Cardiovascular_phenotype": 26,
    "Long_QT_syndrome|Cardiac_arrhythmia": 112,
    "Conduction_disorder_of_the_heart|not_provided": 1,
    "Cardiac_arrhythmia|Cardiomyopathy": 1,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 3,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype": 26,
    "Progressive_familial_heart_block|_type_1A|not_provided|not_specified|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3": 1,
    "Brugada_syndrome_1|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype": 2,
    "not_provided|SCN5A-related_disorder": 2,
    "not_specified|Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|SCN5A-related_disorder": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Cardiomyopathy|Long_QT_syndrome|Brugada_syndrome|Atrial_fibrillation|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Pulmonary_valve_stenosis_(rare)|Ventricular_tachycardia": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Cardiomyopathy|Long_QT_syndrome_2|not_specified|Atrial_fibrillation": 1,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiac_arrhythmia|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided": 37,
    "Brugada_syndrome|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|not_provided|SCN5A-related_disorder": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Cardiomyopathy|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome_1|not_provided|Cardiac_arrhythmia": 3,
    "Congenital_long_QT_syndrome|SCN5A-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome": 8,
    "not_specified|not_provided|Cardiac_arrhythmia": 11,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Left_ventricular_noncompaction_1|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Brugada_syndrome|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided": 5,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "not_provided|SCN5A-related_disorder|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "not_provided|not_specified|Cardiac_arrhythmia": 5,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 30,
    "not_specified|Cardiovascular_phenotype|not_provided|SCN5A-related_disorder|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiac_arrhythmia|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Long_QT_syndrome|Brugada_syndrome_1|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "not_provided|not_specified|Cardiac_arrhythmia|Cardiovascular_phenotype": 7,
    "not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "not_specified|Cardiac_arrhythmia|not_provided": 10,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Death_in_infancy|Brugada_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiac_arrhythmia": 3,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Long_QT_syndrome_3|not_specified": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_specified|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1": 1,
    "not_provided|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|not_provided|Cardiomyopathy|Long_QT_syndrome|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|SCN5A-related_disorder|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_provided": 7,
    "Dilated_cardiomyopathy_1E": 4,
    "not_specified|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 12,
    "Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|not_provided": 3,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Atrial_fibrillation": 1,
    "Cardiac_arrhythmia|not_specified|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3": 1,
    "Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Long_QT_syndrome_3|Cardiac_arrhythmia": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|not_provided": 2,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_1": 2,
    "SCN5A-related_disorder|Cardiac_arrhythmia|not_provided": 1,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|not_provided|Long_QT_syndrome_3": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|Dilated_cardiomyopathy_1E|not_provided|not_specified": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Cardiac_arrhythmia": 1,
    "not_provided|Cardiovascular_phenotype|SCN5A-related_disorder|Cardiac_arrhythmia": 2,
    "SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Primary_dilated_cardiomyopathy|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Atrial_fibrillation|Cardiovascular_phenotype|not_provided": 2,
    "Acquired_long_QT_syndrome": 4,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Cardiac_arrhythmia": 1,
    "Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|not_specified|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "Primary_dilated_cardiomyopathy|Progressive_familial_heart_block|_type_1A|not_provided|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_specified|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_2/3|_digenic|Atrial_fibrillation|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|not_specified": 1,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Cardiovascular_phenotype": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|SCN5A-related_disorder": 1,
    "Cardiac_arrhythmia|not_provided|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Brugada_syndrome_1|not_provided": 1,
    "not_provided|Brugada_syndrome_1|Long_QT_syndrome_3": 2,
    "Long_QT_syndrome_3|Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Brugada_syndrome|Brugada_syndrome_1": 1,
    "not_provided|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|not_provided|Long_QT_syndrome_3|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Brugada_syndrome_1": 1,
    "not_provided|Brugada_syndrome|Cardiac_arrhythmia|Brugada_syndrome_1": 1,
    "Long_QT_syndrome_3|not_provided": 3,
    "Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Congenital_long_QT_syndrome|Brugada_syndrome|SCN5A-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|not_provided|Sinoatrial_node_disorder|Long_QT_syndrome_1": 1,
    "not_specified|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|not_provided|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiomyopathy|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_3": 1,
    "Cardiac_arrhythmia|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Sick_sinus_syndrome_1|Long_QT_syndrome_3|not_provided": 1,
    "Long_QT_syndrome_3": 13,
    "Brugada_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|not_provided|Congenital_long_QT_syndrome": 1,
    "Brugada_syndrome_1|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome_1|not_provided": 9,
    "not_provided|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Brugada_syndrome_1|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|not_provided|Brugada_syndrome": 1,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Brugada_syndrome|Cardiac_arrhythmia": 13,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Sick_sinus_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "Cardiac_arrhythmia|SCN5A-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|SCN5A-related_disorder|Cardiac_arrhythmia|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|SCN5A-related_disorder": 1,
    "not_provided|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "Brugada_syndrome|Brugada_syndrome_1|not_provided": 2,
    "Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|SCN5A-related_disorder|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|not_provided|Brugada_syndrome": 1,
    "not_specified|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|SCN5A-related_disorder": 1,
    "HEART_BLOCK|_NONPROGRESSIVE": 1,
    "not_provided|Cardiac_arrhythmia|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome|not_provided": 1,
    "not_provided|Brugada_syndrome_1": 19,
    "Brugada_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 8,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiac_arrhythmia|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Sudden_cardiac_death|Brugada_syndrome|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia": 4,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|not_provided|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype": 1,
    "not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|not_provided": 2,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|Long_QT_syndrome_3": 4,
    "SCN5A-related_disorder|Cardiac_arrhythmia|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 2,
    "SCN5A-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_3": 1,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "not_provided|Brugada_syndrome_1|Cardiovascular_phenotype|Sudden_unexplained_death|Brugada_syndrome": 1,
    "not_specified|Long_QT_syndrome_3|not_provided|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Brugada_syndrome|not_provided|Conduction_system_disorder|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified": 7,
    "not_provided|Brugada_syndrome|Long_QT_syndrome_3": 1,
    "Brugada_syndrome|Brugada_syndrome_1|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_3|Long_QT_syndrome_3/6|_digenic": 1,
    "Cardiovascular_phenotype|SCN5A-related_disorder|Cardiac_arrhythmia|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided|Brugada_syndrome": 1,
    "not_specified|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 2,
    "Cardiac_arrhythmia|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided|Brugada_syndrome": 1,
    "Conduction_system_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome|Cardiovascular_phenotype|Sick_sinus_syndrome_1|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1E|Congenital_long_QT_syndrome|Brugada_syndrome_1|Long_QT_syndrome_3|not_provided|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_1|Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Long_QT_syndrome_3|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Brugada_syndrome|Brugada_syndrome_1": 4,
    "Brugada_syndrome_1|Brugada_syndrome": 3,
    "Brugada_syndrome|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|not_specified": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_3": 1,
    "Long_QT_syndrome_3|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "not_specified|not_provided|SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Sick_sinus_syndrome_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Long_QT_syndrome_3|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Atrioventricular_block|Atrial_fibrillation|_familial|_10|SCN5A-related_disorder|not_provided|Progressive_familial_heart_block|_type_1A": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder": 1,
    "Cardiac_arrhythmia|Brugada_syndrome": 11,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Brugada_syndrome|Brugada_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_specified|not_provided|Brugada_syndrome": 2,
    "Brugada_syndrome_1|Cardiac_arrhythmia|not_provided": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Brugada_syndrome_1|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|not_provided|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Cardiomyopathy|not_provided": 1,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|not_provided|Dilated_cardiomyopathy_1E": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Long_QT_syndrome|not_provided": 1,
    "Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome": 11,
    "SCN5A-related_disorder|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1|Congenital_long_QT_syndrome|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome": 1,
    "Brugada_syndrome_1|not_provided|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Sick_sinus_syndrome_1|not_specified|Long_QT_syndrome_3|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiac_arrhythmia": 1,
    "not_specified|Congenital_long_QT_syndrome|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1": 2,
    "Cardiac_arrhythmia|SCN5A-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|not_specified|not_provided|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Cardiovascular_phenotype|not_provided|Atrial_fibrillation|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "SCN5A-related_disorder|not_provided": 2,
    "Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided": 2,
    "Brugada_syndrome_1|Long_QT_syndrome_3": 3,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Brugada_syndrome|Cardiac_arrhythmia": 4,
    "Brugada_syndrome|not_provided|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|not_specified|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiac_arrhythmia": 3,
    "Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|not_provided|not_specified|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype|not_provided": 1,
    "Brugada_syndrome|Brugada_syndrome_1|Cardiovascular_phenotype": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A": 1,
    "Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|not_specified|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1": 1,
    "Sick_sinus_syndrome|Congenital_long_QT_syndrome|Primary_dilated_cardiomyopathy|Brugada_syndrome|Long_QT_syndrome|Paroxysmal_familial_ventricular_fibrillation|Progressive_familial_heart_block|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Brugada_syndrome_1": 5,
    "not_provided|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiac_arrhythmia|Brugada_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|not_provided|Brugada_syndrome|Conduction_system_disorder": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Brugada_syndrome|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiomyopathy|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|not_provided": 2,
    "Cardiac_arrhythmia|not_specified|not_provided": 8,
    "Cardiac_arrhythmia|Brugada_syndrome_1|not_provided|Brugada_syndrome": 1,
    "not_provided|not_specified|SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_1": 2,
    "Brugada_syndrome|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Brugada_syndrome": 1,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|not_provided|Progressive_familial_heart_block|_type_1A": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia": 4,
    "Cardiac_arrhythmia|not_specified|Cardiovascular_phenotype|not_provided": 7,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Cardiomyopathy|not_provided|Brugada_syndrome_1": 1,
    "not_provided|Dilated_cardiomyopathy_1E": 3,
    "not_provided|Sick_sinus_syndrome_1": 1,
    "Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|not_provided|Brugada_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_1|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided": 4,
    "Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Brugada_syndrome|Primary_familial_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|SCN5A-related_disorder": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_3|Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome": 1,
    "Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "not_provided|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_(shorter-than-normal_QT_interval)|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|not_provided|Brugada_syndrome": 1,
    "Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Brugada_syndrome_(shorter-than-normal_QT_interval)|Brugada_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Brugada_syndrome|_lidocaine-induced|not_specified|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|not_provided|Brugada_syndrome": 1,
    "Brugada_syndrome_1|not_specified|not_provided|Cardiac_arrhythmia": 1,
    "not_provided|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiac_arrhythmia|SCN5A-related_disorder|Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome|Long_QT_syndrome|Conduction_disorder_of_the_heart|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "See_cases|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Sick_sinus_syndrome|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Sick_sinus_syndrome_1": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1": 1,
    "Cardiac_arrhythmia|not_provided|not_specified|Congenital_long_QT_syndrome": 1,
    "Brugada_syndrome_1|not_provided|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1|not_provided": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Brugada_syndrome|Primary_dilated_cardiomyopathy": 1,
    "SCN5A-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "SCN5A-related_disorder|ATRIAL_STANDSTILL_1|_DIGENIC|Brugada_syndrome|not_provided|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|not_provided": 6,
    "Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_1|not_provided": 1,
    "Progressive_familial_heart_block|_type_1A|not_specified|not_provided|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|not_provided": 6,
    "not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 3,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome": 1,
    "Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|not_provided": 1,
    "not_provided|Brugada_syndrome_1|Brugada_syndrome|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Brugada_syndrome|Brugada_syndrome_1": 3,
    "not_provided|Brugada_syndrome_(shorter-than-normal_QT_interval)": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 2,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided": 2,
    "not_provided|SCN5A-related_disorder|not_specified": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|Brugada_syndrome_1": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1": 2,
    "Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia": 1,
    "Cardiomyopathy|Cardiac_arrhythmia|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Cardiac_arrhythmia": 12,
    "Brugada_syndrome_1|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E": 1,
    "Congenital_long_QT_syndrome|Cardiac_arrhythmia|not_provided": 1,
    "Ventricular_tachycardia|not_provided|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|not_provided|Brugada_syndrome|Cardiomyopathy|Long_QT_syndrome_3|_acquired|_susceptibility_to|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiac_arrhythmia|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Brugada_syndrome_1|not_provided": 2,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|not_specified": 1,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|not_provided": 1,
    "Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 2,
    "Cardiac_arrhythmia|not_provided|Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME": 2,
    "Cardiac_arrhythmia|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 5,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|not_provided": 1,
    "not_provided|Long_QT_syndrome_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Brugada_syndrome|Congenital_heart_disease|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1": 1,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|not_provided|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome": 3,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|SCN5A-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|not_provided": 2,
    "Long_QT_syndrome_3|Brugada_syndrome_1|Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Brugada_syndrome|Long_QT_syndrome_3|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome_1|not_provided|Cardiac_arrhythmia": 1,
    "Progressive_familial_heart_block|_type_1A|not_provided": 1,
    "Atrial_fibrillation|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified|Brugada_syndrome_1": 1,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|not_specified|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Brugada_syndrome_1|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|not_provided|Sick_sinus_syndrome|not_specified|Long_QT_syndrome|Progressive_familial_heart_block|Congenital_long_QT_syndrome": 1,
    "Primary_dilated_cardiomyopathy|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|SCN5A-related_disorder|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|not_specified|Brugada_syndrome|Progressive_familial_heart_block|Paroxysmal_familial_ventricular_fibrillation|not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome": 1,
    "Sick_sinus_syndrome_1": 2,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1|not_specified|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiac_arrhythmia": 1,
    "Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|_acquired|_susceptibility_to|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Brugada_syndrome_1|Congenital_long_QT_syndrome|Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Cardiomyopathy|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|not_provided": 1,
    "not_provided|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|not_provided|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_3|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|not_specified|Brugada_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1": 1,
    "not_provided|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Cardiomyopathy|Long_QT_syndrome_3|not_specified": 1,
    "Cardiac_arrhythmia|not_provided|not_specified|Cardiovascular_phenotype": 2,
    "Brugada_syndrome|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10": 1,
    "Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|not_provided|Long_QT_syndrome|Progressive_familial_heart_block|Sick_sinus_syndrome|Congenital_long_QT_syndrome": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|not_specified|not_provided": 1,
    "SCN5A-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype": 3,
    "Primary_dilated_cardiomyopathy|Cardiac_arrhythmia|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|Dilated_cardiomyopathy_1E|not_provided|not_specified": 1,
    "Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|not_provided|Cardiac_arrhythmia": 1,
    "Brugada_syndrome|not_provided|SCN5A-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|not_provided|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Brugada_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|not_provided|not_specified": 1,
    "not_provided|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|not_provided|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome|Brugada_syndrome_1|Cardiac_arrhythmia|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|SCN5A-related_disorder|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiac_arrhythmia": 1,
    "not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 4,
    "not_provided|Cardiac_arrhythmia|Conduction_system_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Brugada_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Long_QT_syndrome_3|SCN5A-related_disorder|Cardiac_arrhythmia|not_provided": 1,
    "Brugada_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Cardiac_arrhythmia|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|not_provided|Cardiomyopathy": 1,
    "Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Brugada_syndrome|Long_QT_syndrome|Progressive_familial_heart_block|SCN5A-related_disorder|Sick_sinus_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_provided|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiomyopathy": 1,
    "Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome|not_provided": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Brugada_syndrome_(shorter-than-normal_QT_interval)": 2,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3": 1,
    "Cardiac_arrhythmia|SCN5A-related_disorder|Cardiovascular_phenotype|Sudden_cardiac_death|Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Sudden_cardiac_arrest": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|not_specified|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_3|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "not_provided|Long_QT_syndrome_3|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1A|Cardiac_arrhythmia|not_provided": 1,
    "Brugada_syndrome|Progressive_familial_heart_block|Sick_sinus_syndrome|Congenital_long_QT_syndrome|Dilated_Cardiomyopathy|_Dominant|not_provided|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Paroxysmal_familial_ventricular_fibrillation|Long_QT_syndrome": 1,
    "Primary_dilated_cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|not_specified|Sick_sinus_syndrome_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Congenital_long_QT_syndrome|Long_QT_syndrome_3": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Brugada_syndrome|Cardiovascular_phenotype|Ventricular_tachycardia|not_specified": 1,
    "not_provided|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|not_provided|not_specified": 3,
    "Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Cardiovascular_phenotype|not_provided|Brugada_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_1|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 2,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome|Brugada_syndrome_1|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiac_arrhythmia|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|SCN5A-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Brugada_syndrome": 1,
    "not_provided|Brugada_syndrome|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_1|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Congenital_long_QT_syndrome|not_specified|Cardiac_arrhythmia|not_provided": 1,
    "Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Brugada_syndrome_1": 1,
    "SCN5A-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|not_specified|Brugada_syndrome|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Primary_dilated_cardiomyopathy": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "not_provided|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "not_specified|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Cardiac_arrhythmia|Brugada_syndrome_1|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Congenital_long_QT_syndrome|not_specified|not_provided|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome": 4,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Brugada_syndrome_1": 1,
    "Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Primary_dilated_cardiomyopathy|Cardiac_arrhythmia|Cardiomyopathy|Congenital_long_QT_syndrome|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|not_provided": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E": 1,
    "Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Primary_dilated_cardiomyopathy|not_specified|not_provided": 10,
    "not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E": 1,
    "Progressive_familial_heart_block|Sick_sinus_syndrome|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1|Paroxysmal_familial_ventricular_fibrillation|Brugada_syndrome": 1,
    "Cardiac_arrhythmia|not_specified|Brugada_syndrome_1": 1,
    "not_specified|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|Brugada_syndrome|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 168,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Cardiomyopathy|Sudden_cardiac_arrest|Cardiovascular_phenotype|not_specified": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|not_specified|not_provided|Congenital_long_QT_syndrome": 1,
    "Brugada_syndrome_1|Cardiac_arrhythmia|Brugada_syndrome|not_provided": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1|Cardiac_arrhythmia|not_provided": 1,
    "Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|not_provided|SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|not_specified|Brugada_syndrome|not_provided|Cardiomyopathy|Long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|not_provided|Long_QT_syndrome": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|Cardiac_arrhythmia": 1,
    "not_provided|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "SCN5A-related_disorder|not_provided|Cardiac_arrhythmia|Primary_dilated_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|not_provided": 1,
    "Atrial_fibrillation|_familial|_10|Brugada_syndrome|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Brugada_syndrome|not_provided|not_specified": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SCN5A-related_disorder|Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_1|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Atrial_fibrillation|not_provided|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Cardiac_arrhythmia|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Long_QT_syndrome|not_provided|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Brugada_syndrome_1|not_provided|Brugada_syndrome|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1|Cardiac_arrhythmia|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Cardiac_arrest|Sinoatrial_node_disorder|Brugada_syndrome|Brugada_syndrome_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome|SCN5A-related_disorder|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome|not_provided": 1,
    "SCN5A-related_disorder|Cardiac_arrhythmia|not_specified|not_provided|Brugada_syndrome_1": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|not_provided|not_specified|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Brugada_syndrome|not_provided|Brugada_syndrome_1|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|not_provided|not_specified": 1,
    "SCN5A-related_disorder|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Long_QT_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome|_drug-associated|SCN5A-related_disorder|Cardiac_arrhythmia|not_provided|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|_drug-associated|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome_3|Death_in_infancy|Death_in_early_adulthood": 1,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Sick_sinus_syndrome_1|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|not_provided|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Cardiac_arrhythmia|Sudden_unexplained_death|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Cardiovascular_phenotype|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|SCN5A-related_disorder|not_specified|Cardiomyopathy|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1|not_provided|Progressive_familial_heart_block|_type_1A": 1,
    "not_specified|Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified": 2,
    "not_specified|Cardiomyopathy|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrest|Congenital_long_QT_syndrome|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiac_arrhythmia|SCN5A-related_disorder|Cardiovascular_phenotype|not_specified|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Congenital_long_QT_syndrome|Cardiomyopathy|not_specified|Long_QT_syndrome|Brugada_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome|not_provided|SCN5A-related_disorder|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "not_provided|Congenital_long_QT_syndrome|SCN5A-related_disorder|Cardiac_arrhythmia|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Wolff-Parkinson-White_pattern": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Cardiac_arrhythmia|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|Autism|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1": 1,
    "Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|not_specified|Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiomyopathy|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Sudden_cardiac_arrest|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|SCN5A-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|Brugada_syndrome_1|not_provided|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E": 1,
    "Sick_sinus_syndrome_1|Cardiac_arrhythmia": 1,
    "Congenital_long_QT_syndrome|Brugada_syndrome_1|not_specified|Cardiac_arrhythmia|Long_QT_syndrome_3|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Primary_familial_dilated_cardiomyopathy|Brugada_syndrome": 1,
    "Paroxysmal_familial_ventricular_fibrillation|Progressive_familial_heart_block|Dilated_Cardiomyopathy|_Dominant|Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Sick_sinus_syndrome|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|not_provided|Brugada_syndrome|Cardiomyopathy|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Brugada_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Brugada_syndrome|Primary_familial_hypertrophic_cardiomyopathy|Brugada_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|not_specified|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome|Brugada_syndrome_1|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|not_specified|not_provided|Cardiomyopathy": 1,
    "Progressive_familial_heart_block|Cardiac_arrhythmia|Paroxysmal_familial_ventricular_fibrillation|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Sick_sinus_syndrome|Congenital_long_QT_syndrome|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|Brugada_syndrome_1": 2,
    "Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Congenital_long_QT_syndrome|not_provided|Wolff-Parkinson-White_pattern": 1,
    "Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|SCN5A-related_disorder": 1,
    "CARDIAC_CONDUCTION_DEFECT|_NONPROGRESSIVE|Conduction_system_disorder": 1,
    "Brugada_syndrome_1|Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiac_arrhythmia|SCN5A-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Cardiac_arrhythmia|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided|Conduction_system_disorder": 1,
    "not_provided|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|not_specified|Cardiac_arrhythmia|Brugada_syndrome": 1,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3": 1,
    "Congenital_long_QT_syndrome|not_provided|Progressive_familial_heart_block|_type_1A|Cardiac_arrhythmia|Cardiovascular_phenotype|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|not_specified|not_provided": 2,
    "Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Cardiac_arrhythmia|not_provided": 1,
    "Long_QT_syndrome_3|Brugada_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiac_arrhythmia|Atrial_fibrillation|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|not_provided": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "not_provided|Long_QT_syndrome_3|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sudden_cardiac_death|not_specified|not_provided": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1": 3,
    "Cardiac_arrhythmia|not_specified|not_provided|Cardiovascular_phenotype|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Brugada_syndrome_1|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Sick_sinus_syndrome_1|not_specified|Cardiomyopathy|SCN5A-related_disorder|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_1|Cardiovascular_phenotype|Atrial_fibrillation|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|not_provided|not_specified|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Cardiomyopathy|Brugada_syndrome_1|Cardiovascular_phenotype|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Cardiac_arrhythmia|Primary_dilated_cardiomyopathy": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|not_provided": 1,
    "Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Atrial_fibrillation|not_specified|SCN5A-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Cardiomyopathy": 1,
    "Syncope": 1,
    "Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiac_arrhythmia|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Long_QT_syndrome_3|Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Congenital_long_QT_syndrome|SCN5A-related_disorder": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype": 5,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_3|SCN5A-related_disorder": 1,
    "Ventricular_fibrillation": 4,
    "Congenital_long_QT_syndrome|not_provided|not_specified|Cardiac_arrhythmia": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A": 1,
    "Progressive_familial_heart_block|_type_1A|not_provided|Sick_sinus_syndrome_1|Brugada_syndrome_1|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_specified|Dilated_cardiomyopathy_1E|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia": 1,
    "SCN5A-related_disorder|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|not_provided|Brugada_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_1|not_specified": 1,
    "Congenital_long_QT_syndrome|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|not_provided|SCN5A-related_disorder|Cardiovascular_phenotype|Brugada_syndrome|Brugada_syndrome_1": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Brugada_syndrome|Cardiac_arrhythmia|Long_QT_syndrome|Sick_sinus_syndrome|Primary_dilated_cardiomyopathy|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Brugada_syndrome|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided": 1,
    "Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|SCN5A-related_disorder|not_specified|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1": 1,
    "not_specified|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome_1|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|not_specified|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Brugada_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Familial_sick_sinus_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_provided|Cardiac_arrhythmia|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Long_QT_syndrome_3|Brugada_syndrome_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|not_provided|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E": 1,
    "Brugada_syndrome_(shorter-than-normal_QT_interval)|SCN5A-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder": 1,
    "Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|not_provided|not_specified|Atrioventricular_block|Migraine|Primary_dilated_cardiomyopathy|Hemiplegia": 1,
    "Cardiac_arrhythmia|Sudden_cardiac_death": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|not_provided|not_specified": 1,
    "Cardiac_arrhythmia|not_specified|Brugada_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "not_provided|Brugada_syndrome|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "not_provided|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Torsades_de_pointes|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Long_QT_syndrome|not_provided|Cardiac_arrhythmia|Brugada_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_1": 1,
    "not_specified|Brugada_syndrome|not_provided": 11,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|not_specified|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|Long_QT_syndrome_3|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "not_provided|Brugada_syndrome_1|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Brugada_syndrome|Brugada_syndrome|_lidocaine-induced|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Conduction_system_disorder|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome|Paroxysmal_familial_ventricular_fibrillation|Dilated_Cardiomyopathy|_Dominant|Long_QT_syndrome|Progressive_familial_heart_block|Congenital_long_QT_syndrome|Sick_sinus_syndrome": 1,
    "Heart_failure": 2,
    "Brugada_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|not_specified|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Brugada_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Congenital_long_QT_syndrome|not_provided|Brugada_syndrome|Conduction_system_disorder": 1,
    "Congenital_long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_3|not_provided|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E": 1,
    "SCN5A-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|Brugada_syndrome_1|Long_QT_syndrome_3|Primary_familial_dilated_cardiomyopathy|AV_junctional_rhythm|not_specified|not_provided|Brugada_syndrome|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1": 1,
    "Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Cardiomyopathy": 1,
    "Brugada_syndrome|Brugada_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Dilated_cardiomyopathy_1E|not_provided|Cardiovascular_phenotype": 1,
    "Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|not_specified|Brugada_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Ventricular_tachycardia": 1,
    "Congenital_long_QT_syndrome|ATRIAL_STANDSTILL_1|_DIGENIC|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Cardiomyopathy|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided": 1,
    "Sick_sinus_syndrome_1|Cardiac_arrhythmia|Brugada_syndrome|not_provided": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|SCN5A-related_disorder|Cardiomyopathy": 1,
    "Cardiac_arrhythmia|not_provided|Brugada_syndrome_1": 2,
    "Cardiovascular_phenotype|Brugada_syndrome|not_provided|Cardiac_arrhythmia|SCN5A-related_disorder|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Brugada_syndrome|Cardiovascular_phenotype|not_provided|Brugada_syndrome_1": 1,
    "not_specified|Brugada_syndrome_1": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_3|Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome|Brugada_syndrome_1|not_provided|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Brugada_syndrome_1|Sick_sinus_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|not_specified": 1,
    "not_provided|Cardiac_arrest": 1,
    "not_provided|Brugada_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Brugada_syndrome_1|not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided|Brugada_syndrome": 1,
    "Brugada_syndrome|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Sick_sinus_syndrome_1|Long_QT_syndrome_3|not_provided|not_specified|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A": 1,
    "Cardiac_arrhythmia|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Brugada_syndrome|not_provided": 1,
    "Primary_dilated_cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Brugada_syndrome|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "SCN5A-related_disorder|Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_1|Long_QT_syndrome_3|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Progressive_familial_heart_block|_type_1A|Sick_sinus_syndrome_1": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10": 1,
    "SCN5A-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Brugada_syndrome|not_provided|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|SCN5A-related_disorder|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Cardiac_arrhythmia|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|SUDDEN_INFANT_DEATH_SYNDROME|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|SCN5A-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|not_provided|Cardiac_arrhythmia|not_specified": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Brugada_syndrome_1|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Brugada_syndrome_1|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Brugada_syndrome|not_provided|Brugada_syndrome_1|Cardiovascular_phenotype|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Atrial_fibrillation|_familial|_10": 1,
    "not_specified|not_provided|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Long_QT_syndrome_3|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided|Brugada_syndrome": 1,
    "not_provided|Brugada_syndrome|Sick_sinus_syndrome_1|Brugada_syndrome_1|Cardiovascular_phenotype|Brugada_syndrome_(shorter-than-normal_QT_interval)|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Long_QT_syndrome_3|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|not_specified|not_provided": 1,
    "Sick_sinus_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided": 1,
    "not_specified|Brugada_syndrome|SCN5A-related_disorder|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia|not_provided": 1,
    "Long_QT_syndrome_3|not_provided|Cardiac_arrhythmia": 1,
    "not_provided|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome_1|Atrial_fibrillation|_familial|_10|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1": 1,
    "Cardiac_arrhythmia|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Brugada_syndrome_1|not_specified|Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10": 1,
    "Congenital_long_QT_syndrome|not_provided|Hypertrophic_cardiomyopathy|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome_3|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_specified|SCN5A-related_disorder|not_provided|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_1|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|SCN5A-related_disorder": 1,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Long_QT_syndrome_3|Cardiac_arrhythmia|Brugada_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Congenital_long_QT_syndrome|not_provided|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Sick_sinus_syndrome_1|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_3|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|SCN5A-related_disorder|Cardiac_arrhythmia|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome_3|Sick_sinus_syndrome_1|Brugada_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Atrial_fibrillation|_familial|_10|not_provided": 1,
    "Cardiac_arrhythmia|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|SUDDEN_INFANT_DEATH_SYNDROME|Progressive_familial_heart_block|_type_1A|Long_QT_syndrome_3|Dilated_cardiomyopathy_1E|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Brugada_syndrome_1|Brugada_syndrome|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Brugada_syndrome_1|Death_in_infancy|Congenital_long_QT_syndrome": 1,
    "not_provided|SCN5A-related_disorder|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Atrial_fibrillation|_familial|_10|Brugada_syndrome_1|Sick_sinus_syndrome_1|Ventricular_fibrillation|_paroxysmal_familial|_type_1|SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|not_specified|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Brugada_syndrome_1|Long_QT_syndrome_3": 1,
    "Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|Dilated_cardiomyopathy_1E|Brugada_syndrome_1|Long_QT_syndrome_3|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Long_QT_syndrome_3|Brugada_syndrome_1|not_specified|Dilated_cardiomyopathy_1E|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Atrial_fibrillation|_familial|_10|Sick_sinus_syndrome_1|Progressive_familial_heart_block|_type_1A|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|SCN5A-related_disorder": 1,
    "not_provided|Congenital_long_QT_syndrome|Progressive_familial_heart_block|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Paroxysmal_familial_ventricular_fibrillation|Cardiac_arrhythmia|Sick_sinus_syndrome|Brugada_syndrome|Long_QT_syndrome": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Progressive_familial_heart_block|_type_1A|Brugada_syndrome_1|Dilated_cardiomyopathy_1E|Sick_sinus_syndrome_1|Brugada_syndrome|Long_QT_syndrome_3|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_10|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_specified|not_provided|Brugada_syndrome": 2,
    "not_provided|not_specified|Brugada_syndrome|SCN10A-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_1": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2": 7,
    "Episodic_pain_syndrome|_familial|_2": 14,
    "Brugada_syndrome|Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|not_provided": 3,
    "not_specified|Brugada_syndrome|not_provided|Cardiovascular_phenotype": 2,
    "SCN10A-related_disorder": 8,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype|SCN10A-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|SCN10A-related_disorder|Brugada_syndrome": 2,
    "not_provided|not_specified|Cardiovascular_phenotype|Brugada_syndrome": 4,
    "Cardiovascular_phenotype|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2": 9,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome|not_provided": 3,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome": 7,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_provided|Brugada_syndrome": 4,
    "Brugada_syndrome_1|Episodic_pain_syndrome|_familial|_2|not_specified|Cardiovascular_phenotype|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome": 6,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2": 1,
    "Episodic_pain_syndrome|_familial|_2|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Impaired_temperature_sensation|Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|Brugada_syndrome|not_specified|Brugada_syndrome_1": 1,
    "Brugada_syndrome|not_provided|SCN10A-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|not_specified|Cardiovascular_phenotype": 13,
    "not_specified|not_provided|Cardiovascular_phenotype|Brugada_syndrome": 4,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype|not_provided|Hereditary_sodium_channelopathy-related_small_fibers_neuropathy": 1,
    "Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|Brugada_syndrome|not_provided|not_specified": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|SCN10A-related_disorder": 3,
    "Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|Brugada_syndrome": 7,
    "Cardiovascular_phenotype|Brugada_syndrome_1|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome": 3,
    "Cardiovascular_phenotype|SCN10A-related_disorder|Brugada_syndrome|not_specified": 1,
    "SCN10A-related_disorder|not_provided|Cardiovascular_phenotype|not_specified|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_specified|not_provided": 4,
    "not_provided|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|See_cases|Brugada_syndrome": 1,
    "SCN10A-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome": 2,
    "Brugada_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 4,
    "Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|not_provided|Brugada_syndrome": 1,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "SCN10A-related_disorder|not_provided|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome|not_provided|SCN10A-related_disorder": 1,
    "Brugada_syndrome|not_specified|Episodic_pain_syndrome|_familial|_2": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|not_specified": 4,
    "SCN10A-related_disorder|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|SCN10A-related_disorder": 6,
    "Episodic_pain_syndrome|_familial|_2|not_provided": 1,
    "Brugada_syndrome|SCN10A-related_disorder|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_specified|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|not_provided": 1,
    "not_provided|SCN10A-related_disorder|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "SCN10A-related_disorder|Brugada_syndrome": 1,
    "Brugada_syndrome|not_provided|Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_provided|not_specified": 2,
    "not_specified|Brugada_syndrome|SCN10A-related_disorder": 1,
    "Cardiovascular_phenotype|SCN10A-related_disorder|not_provided|not_specified|Brugada_syndrome|Brugada_syndrome_1": 1,
    "not_specified|Brugada_syndrome|SCN10A-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2": 1,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_specified": 1,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype|not_provided": 4,
    "Episodic_pain_syndrome|_familial|_2|not_provided|Brugada_syndrome|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|SCN10A-related_disorder|Brugada_syndrome": 1,
    "not_provided|Episodic_pain_syndrome|_familial|_2|not_specified|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|SCN10A-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|not_specified|Episodic_pain_syndrome|_familial|_2": 1,
    "Episodic_pain_syndrome|_familial|_2|not_provided|not_specified|Brugada_syndrome|Cardiovascular_phenotype": 3,
    "not_provided|not_specified|Brugada_syndrome|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2": 1,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome": 8,
    "Brugada_syndrome|Episodic_pain_syndrome|_familial|_2|not_specified|not_provided": 1,
    "not_provided|not_specified|Brugada_syndrome|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|not_provided|not_specified|Brugada_syndrome": 1,
    "Brugada_syndrome|not_specified|not_provided": 8,
    "not_provided|not_specified|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome": 2,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype": 4,
    "Brugada_syndrome|Episodic_pain_syndrome|_familial|_2|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Episodic_pain_syndrome|_familial|_2": 2,
    "Episodic_pain_syndrome|_familial|_2|not_specified|not_provided|Brugada_syndrome|Cardiovascular_phenotype": 2,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2": 1,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2": 1,
    "not_provided|SCN10A-related_disorder|Cardiovascular_phenotype|Brugada_syndrome|not_specified": 1,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2": 2,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome": 1,
    "not_provided|Episodic_pain_syndrome|_familial|_2|not_specified|Brugada_syndrome|Cardiovascular_phenotype|Brugada_syndrome_1": 1,
    "not_provided|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Brugada_syndrome|SCN10A-related_disorder": 1,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|not_provided|Cardiovascular_phenotype": 3,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome|SCN10A-related_disorder": 1,
    "Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_specified|Brugada_syndrome": 1,
    "not_provided|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype": 2,
    "Episodic_pain_syndrome|_familial|_2|not_specified|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "not_provided|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome": 1,
    "Brugada_syndrome|SCN10A-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "SCN10A-related_disorder|Brugada_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|not_provided|not_specified": 1,
    "Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|not_provided": 1,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|not_specified": 1,
    "Episodic_pain_syndrome|_familial|_2|not_specified|Brugada_syndrome|SCN10A-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|SCN10A-related_disorder|Brugada_syndrome|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Episodic_pain_syndrome|_familial|_2|SCN10A-related_disorder|Brugada_syndrome|not_provided": 1,
    "Episodic_pain_syndrome|_familial|_2|not_provided|Brugada_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Brugada_syndrome": 3,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype|SCN10A-related_disorder": 1,
    "not_specified|not_provided|Brugada_syndrome|Cardiovascular_phenotype|Brugada_syndrome_1": 1,
    "not_specified|not_provided|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Brugada_syndrome|Cardiovascular_phenotype|SCN10A-related_disorder|Episodic_pain_syndrome|_familial|_2": 1,
    "not_provided|Brugada_syndrome|not_specified": 2,
    "not_provided|Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2": 1,
    "SCN10A-related_disorder|Cardiovascular_phenotype|Brugada_syndrome": 4,
    "Cardiovascular_phenotype|Brugada_syndrome|Episodic_pain_syndrome|_familial|_2|not_specified|not_provided": 1,
    "SCN10A-related_disorder|Brugada_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Brugada_syndrome|not_provided|SCN10A-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "SCN10A-related_disorder|Brugada_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|not_specified|SCN10A-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_1|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_1|not_provided|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Brugada_syndrome_1|Episodic_pain_syndrome|_familial|_2|Brugada_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype": 1,
    "not_provided|Brugada_syndrome_1|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Brugada_syndrome|not_provided|SCN10A-related_disorder": 1,
    "not_provided|Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Brugada_syndrome_1|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Brugada_syndrome|SCN10A-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Episodic_pain_syndrome|_familial|_2|Cardiovascular_phenotype|Brugada_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Episodic_pain_syndrome|_familial|_2|not_provided|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|Inborn_genetic_diseases": 24,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 65,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases": 64,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided": 14,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 717,
    "Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 238,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided": 27,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|SCN11A-related_disorder|not_provided": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases": 7,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 25,
    "not_provided|Inborn_genetic_diseases|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 1,
    "not_provided|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|Inborn_genetic_diseases": 2,
    "Hereditary_motor_neuron_disease|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|SCN11A-related_disorder": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 25,
    "SCN11A-related_disorder": 7,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases|not_provided": 7,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided|SCN11A-related_disorder": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|SCN11A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Sensory_neuropathy|Inborn_genetic_diseases": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases|SCN11A-related_disorder": 4,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Charcot-Marie-Tooth_disease": 1,
    "Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|not_provided": 5,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified": 2,
    "Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified|not_provided": 2,
    "not_provided|SCN11A-related_disorder|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 2,
    "not_specified|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided": 1,
    "not_provided|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 4,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Charcot-Marie-Tooth_disease": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7": 5,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided|Inborn_genetic_diseases": 4,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|SCN11A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "SCN11A-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 3,
    "Inborn_genetic_diseases|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_7": 1,
    "not_provided|not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 2,
    "Inborn_genetic_diseases|not_provided|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 5,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 2,
    "SCN11A-related_disorder|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 2,
    "SCN11A-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases": 1,
    "See_cases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified|Inborn_genetic_diseases": 1,
    "Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 3,
    "SCN11A-related_disorder|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided": 1,
    "not_provided|SCN11A-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_specified|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Inborn_genetic_diseases": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Charcot-Marie-Tooth_disease|Limb-girdle_muscular_dystrophy": 1,
    "Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|SCN11A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|SCN11A-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_7|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|SCN11A-related_disorder|not_specified|not_provided": 1,
    "not_specified|Familial_episodic_pain_syndrome_with_predominantly_lower_limb_involvement|Hereditary_sensory_and_autonomic_neuropathy_type_7|SCN11A-related_disorder": 1,
    "WDR48-related_disorder": 9,
    "WDR48-related_disorder|not_provided|Hereditary_spastic_paraplegia": 1,
    "TTC21A-related_disorder|not_specified": 2,
    "TTC21A-related_disorder": 21,
    "Spermatogenic_failure_37": 7,
    "not_provided|TTC21A-related_disorder": 2,
    "TTC21A-related_disorder|not_provided": 2,
    "XIRP1-related_disorder": 35,
    "not_provided|XIRP1-related_disorder": 13,
    "XIRP1-related_disorder|not_provided": 11,
    "XIRP1-related_disorder|not_specified": 2,
    "Classical_primary_microcephaly|not_specified": 1,
    "not_specified|XIRP1-related_disorder": 3,
    "XIRP1-related_disorder|not_specified|not_provided": 1,
    "CX3CR1-related_disorder": 3,
    "CX3CR1-related_disorder|not_provided": 1,
    "CX3CR1-related_disorder|not_provided|Susceptibility_to_HIV_infection|Coronary_heart_disease|_susceptibility_to|_1|Age_related_macular_degeneration_12": 1,
    "X-linked_sideroblastic_anemia_1|Sideroblastic_anemia_2": 6,
    "not_provided|X-linked_sideroblastic_anemia_1|Sideroblastic_anemia_2": 3,
    "Sideroblastic_anemia_2|not_provided": 12,
    "not_provided|Sideroblastic_anemia_2|Refractory_anemia_with_ringed_sideroblasts": 1,
    "Sideroblastic_anemia_2|Refractory_anemia_with_ringed_sideroblasts|not_provided": 4,
    "Sideroblastic_anemia_2": 59,
    "X-linked_sideroblastic_anemia_1|not_provided|Sideroblastic_anemia_2": 1,
    "SLC25A38-related_disorder|not_provided": 1,
    "not_provided|X-linked_sideroblastic_anemia_1|Inborn_genetic_diseases|Sideroblastic_anemia_2": 1,
    "Refractory_anemia_with_ringed_sideroblasts|not_specified|not_provided|Sideroblastic_anemia_2": 1,
    "not_provided|Sideroblastic_anemia_2": 6,
    "not_provided|Sideroblastic_anemia_2|SLC25A38-related_disorder": 1,
    "Inborn_genetic_diseases|Sideroblastic_anemia_2|not_provided": 1,
    "not_specified|X-linked_sideroblastic_anemia_1|Inborn_genetic_diseases|not_provided|Sideroblastic_anemia_2": 1,
    "Sideroblastic_anemia_2|Inborn_genetic_diseases|not_provided": 1,
    "SLC25A38-related_disorder|not_provided|Sideroblastic_anemia_2": 1,
    "not_provided|X-linked_sideroblastic_anemia_1|Sideroblastic_anemia_2|SLC25A38-related_disorder|not_specified": 1,
    "X-linked_sideroblastic_anemia_1|Sideroblastic_anemia_2|Inborn_genetic_diseases": 1,
    "Sideroblastic_anemia_2|SLC25A38-related_disorder|not_specified|not_provided": 1,
    "Refractory_anemia_with_ringed_sideroblasts|Sideroblastic_anemia_2": 1,
    "Refractory_anemia_with_ringed_sideroblasts|Sideroblastic_anemia_2|not_provided|Inborn_genetic_diseases": 1,
    "Sideroblastic_anemia_2|X-linked_sideroblastic_anemia_1": 2,
    "Refractory_anemia_with_ringed_sideroblasts|Sideroblastic_anemia_2|not_provided": 1,
    "Sideroblastic_anemia_2|Refractory_anemia_with_ringed_sideroblasts": 2,
    "not_provided|Sideroblastic_anemia_2|X-linked_sideroblastic_anemia_1": 1,
    "Refractory_anemia_with_ringed_sideroblasts|X-linked_sideroblastic_anemia_1": 1,
    "X-linked_sideroblastic_anemia_1|Refractory_anemia_with_ringed_sideroblasts": 1,
    "not_provided|Familial_isolated_congenital_asplenia|not_specified": 2,
    "Familial_isolated_congenital_asplenia": 7,
    "not_provided|Familial_isolated_congenital_asplenia": 3,
    "RPSA-related_disorder": 2,
    "RPSA-related_disorder|not_provided": 2,
    "not_provided|RPSA-related_disorder": 2,
    "Familial_isolated_congenital_asplenia|not_provided": 1,
    "MOBP-related_disorder": 11,
    "CTNNB1-related_disorder": 14,
    "CTNNB1-related_syndromic_intellectual_disability": 2,
    "not_specified|Medulloblastoma|Pilomatrixoma|Ovarian_neoplasm|Colorectal_cancer|Exudative_vitreoretinopathy_7|Hepatocellular_carcinoma|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|not_provided": 1,
    "Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 71,
    "not_provided|CTNNB1-related_disorder": 6,
    "Juvenile_nasopharyngeal_angiofibroma": 2,
    "Pilomatrixoma|Hepatoblastoma|Medulloblastoma": 1,
    "Pilomatrixoma|not_provided": 1,
    "Pilomatrixoma|Carcinoma_of_colon": 1,
    "Malignant_tumor_of_urinary_bladder|Pilomatrixoma|Medulloblastoma|Adrenal_cortex_neoplasm": 1,
    "Pilomatrixoma|Medulloblastoma": 1,
    "Prostate_cancer|Hepatoblastoma": 1,
    "not_provided|Pilomatrixoma|Ovarian_neoplasm": 1,
    "Pilomatrixoma": 1,
    "Hepatocellular_carcinoma|Exudative_vitreoretinopathy_7|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Ovarian_cancer|Medulloblastoma|Colorectal_cancer|Pilomatrixoma|Atypical_endometrial_hyperplasia|not_provided|Hepatoblastoma|Desmoid_tumor_caused_by_somatic_mutation|Desmoid_tumor": 1,
    "Pilomatrixoma|Desmoid_disease|_hereditary": 1,
    "Nephroblastoma|Carcinoma_of_colon": 1,
    "not_provided|Hepatocellular_carcinoma": 1,
    "Gallbladder_cancer|Nephroblastoma|Hepatocellular_carcinoma": 1,
    "not_provided|Conspicuously_happy_disposition": 1,
    "not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 8,
    "Inborn_genetic_diseases|not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|CTNNB1-related_disorder|Pilomatrixoma|Medulloblastoma|Ovarian_neoplasm|Hepatocellular_carcinoma|Exudative_vitreoretinopathy_7|Carcinoma_of_colon": 1,
    "Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|not_provided": 6,
    "CTNNB1-related_disorder|not_provided": 7,
    "CTNNB1-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|CTNNB1-related_disorder": 1,
    "CTNNB1-related_disorder|not_provided|not_specified": 1,
    "CTNNB1-related_disorder|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 1,
    "CTNNB1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hepatocellular_carcinoma": 1,
    "Increased_bone_mineral_density": 3,
    "CTNNB1-related_disorder|not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Hepatocellular_carcinoma": 1,
    "not_specified|not_provided|CTNNB1-related_disorder": 1,
    "Hepatocellular_carcinoma|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 1,
    "Colorectal_cancer|not_provided": 24,
    "Exudative_vitreoretinopathy_7": 3,
    "Inborn_genetic_diseases|Exudative_vitreoretinopathy_7": 1,
    "not_specified|not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Hepatocellular_carcinoma|Pilomatrixoma|Ovarian_neoplasm|Colorectal_cancer|Medulloblastoma|Exudative_vitreoretinopathy_7": 1,
    "CTNNB1-related_syndromic_intellectual_disability|not_provided": 1,
    "Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|CTNNB1-related_disorder": 1,
    "Medulloblastoma|Pilomatrixoma|Ovarian_neoplasm|Exudative_vitreoretinopathy_7|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Hepatocellular_carcinoma|Colorectal_cancer|Neurodevelopmental_disorder|not_provided|Developmental_disorder|Microcephalic_primordial_dwarfism|_Alazami_type|Intellectual_disability": 1,
    "Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Exudative_vitreoretinopathy_1": 1,
    "not_provided|Autosomal_dominant_polycystic_liver_disease": 6,
    "Hepatocellular_carcinoma|not_provided": 1,
    "Medulloblastoma|Exudative_vitreoretinopathy_7|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Colorectal_cancer|Pilomatrixoma|Hepatocellular_carcinoma|Ovarian_neoplasm|not_provided": 1,
    "not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Exudative_vitreoretinopathy_7|Ovarian_neoplasm|Hepatocellular_carcinoma|Medulloblastoma|Pilomatrixoma|Colorectal_cancer": 1,
    "Abnormal_lung_growth|_pulmonary_hypertension|_microcephaly|_and_spasticity|Intellectual_disability|Exudative_vitreoretinopathy_7|not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome": 1,
    "not_provided|Medulloblastoma|Pilomatrixoma|Colorectal_cancer|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Exudative_vitreoretinopathy_7|Ovarian_neoplasm|Hepatocellular_carcinoma": 1,
    "Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|CTNNB1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Intellectual_disability": 1,
    "Global_developmental_delay|Microcephaly|Imperforate_anus|Teratoma|Absent_speech": 1,
    "not_provided|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|not_provided|Global_developmental_delay|CTNNB1-related_disorder": 1,
    "Exudative_vitreoretinopathy_7|Exudative_vitreoretinopathy_1|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_7": 1,
    "Exudative_vitreoretinopathy_7|Exudative_vitreoretinopathy_1": 1,
    "Autosomal_dominant_polycystic_liver_disease": 81,
    "Ovarian_neoplasm|Severe_intellectual_disability-progressive_spastic_diplegia_syndrome|Pilomatrixoma|Hepatocellular_carcinoma|Exudative_vitreoretinopathy_7|Colorectal_cancer|Medulloblastoma|not_specified|not_provided": 1,
    "ULK4-related_disorder": 18,
    "ULK4-related_disorder|Intellectual_disability|_moderate": 2,
    "not_specified|ULK4-related_disorder": 1,
    "not_provided|ULK4-related_disorder": 1,
    "ULK4-related_disorder|not_provided|Intellectual_disability|_moderate": 1,
    "ULK4-related_disorder|not_provided": 2,
    "not_provided|TRAK1-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_68": 9,
    "TRAK1-related_disorder|not_provided": 10,
    "not_provided|TRAK1-related_disorder": 11,
    "not_provided|Developmental_and_epileptic_encephalopathy|_68|Inborn_genetic_diseases": 1,
    "TRAK1-related_disorder": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy|_68": 5,
    "Developmental_and_epileptic_encephalopathy|_68|not_provided": 7,
    "Developmental_and_epileptic_encephalopathy|_68|Inborn_genetic_diseases": 2,
    "not_provided|TRAK1-related_disorder|Developmental_and_epileptic_encephalopathy|_68|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_68": 1,
    "Developmental_and_epileptic_encephalopathy|_68|not_specified": 1,
    "Inborn_genetic_diseases|TRAK1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_68|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|TRAK1-related_disorder": 1,
    "ZBTB47-related_condition": 1,
    "Neurodevelopmental_delay|Seizure|ZBTB47-related_disorder": 1,
    "Nemaline_myopathy_8": 347,
    "Inborn_genetic_diseases|Nemaline_myopathy_8": 25,
    "Nemaline_myopathy_8|not_provided": 20,
    "Inborn_genetic_diseases|Nemaline_myopathy_8|not_provided": 6,
    "Nemaline_myopathy_8|Inborn_genetic_diseases": 20,
    "Nemaline_myopathy_8|not_specified|not_provided": 5,
    "not_provided|KLHL40-related_disorder|Nemaline_myopathy_8": 1,
    "not_specified|Nemaline_myopathy_8|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Nemaline_myopathy_8": 4,
    "Nemaline_myopathy_8|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Nemaline_myopathy_8|Inborn_genetic_diseases": 2,
    "not_provided|Nemaline_myopathy_8": 5,
    "Nemaline_myopathy_8|not_provided|not_specified|KLHL40-related_disorder": 1,
    "Nemaline_myopathy_8|Inborn_genetic_diseases|not_provided": 2,
    "KLHL40-related_disorder": 5,
    "Nemaline_myopathy_8|not_provided|KLHL40-related_disorder": 1,
    "not_provided|Nemaline_myopathy_8|not_specified": 4,
    "KLHL40-related_disorder|Nemaline_myopathy_8": 4,
    "Nemaline_myopathy_8|not_specified": 4,
    "not_specified|not_provided|Nemaline_myopathy_8": 2,
    "Nemaline_myopathy_8|KLHL40-related_disorder": 3,
    "not_specified|Nemaline_myopathy_8|KLHL40-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Nemaline_myopathy_8": 1,
    "KLHL40-related_disorder|Nemaline_myopathy_8|not_provided": 1,
    "not_provided|not_specified|Nemaline_myopathy_8": 1,
    "HHATL-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 268,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 2,
    "Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases": 17,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 4,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 3,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 18,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided": 12,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 20,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "not_provided|POMGNT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases|not_provided": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_specified": 3,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases": 5,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|Inborn_genetic_diseases": 3,
    "Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|not_specified": 3,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided": 2,
    "POMGNT2-related_disorder|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|concomitant_exotropia": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases": 1,
    "POMGNT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases|not_provided": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|Inborn_genetic_diseases|POMGNT2-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_specified|not_provided": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_specified|Inborn_genetic_diseases": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8": 1,
    "Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8": 2,
    "POMGNT2-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Severe_hydrocephalus|Neonatal_death": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|POMGNT2-related_disorder": 1,
    "POMGNT2-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|POMGNT2-related_disorder|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|Inborn_genetic_diseases": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_provided|POMGNT2-related_disorder": 1,
    "POMGNT2-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "not_specified|not_provided|POMGNT2-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "not_specified|POMGNT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|not_specified|Muscular_dystrophy-dystroglycanopathy_(limb-girdle)|_type_C|_8|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_10": 53,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_10": 26,
    "Autosomal_recessive_spinocerebellar_ataxia_10|not_provided": 14,
    "Autosomal_recessive_spinocerebellar_ataxia_10|ANO10-related_disorder|not_specified|not_provided": 1,
    "not_provided|ANO10-related_disorder": 2,
    "not_provided|not_specified|ANO10-related_disorder": 1,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_10": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_10": 3,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "not_provided|not_specified|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_10|not_provided": 3,
    "Autosomal_recessive_spinocerebellar_ataxia_10|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_10|not_specified": 5,
    "Autosomal_recessive_cerebellar_ataxia|not_provided": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_10|not_provided|not_specified": 1,
    "ANO10-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_10|ANO10-related_disorder|not_provided": 1,
    "ANO10-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_10|Inborn_genetic_diseases": 1,
    "ANO10-related_disorder": 2,
    "ANO10-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_10|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_10|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_10|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_cerebellar_ataxia|Abnormal_central_motor_function|not_provided|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_10": 1,
    "Triglyceride_storage_disease_with_ichthyosis": 116,
    "not_provided|Triglyceride_storage_disease_with_ichthyosis": 15,
    "ABHD5-related_disorder|Triglyceride_storage_disease_with_ichthyosis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ABHD5-related_disorder|not_provided|Triglyceride_storage_disease_with_ichthyosis": 2,
    "not_provided|ABHD5-related_disorder": 1,
    "ABHD5-related_disorder": 1,
    "Triglyceride_storage_disease_with_ichthyosis|not_provided": 7,
    "Triglyceride_storage_disease_with_ichthyosis|ABHD5-related_disorder|not_provided": 1,
    "ABHD5-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Triglyceride_storage_disease_with_ichthyosis": 2,
    "not_provided|Triglyceride_storage_disease_with_ichthyosis|ABHD5-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Triglyceride_storage_disease_with_ichthyosis": 1,
    "Pulmonary_fibrosis": 46,
    "Braddock-carey_syndrome_2": 3,
    "Macular_dystrophy|_retinal|_4": 1,
    "LARS2-related_disorder|not_provided|not_specified": 2,
    "Perrault_syndrome_4": 23,
    "LARS2-related_disorder|not_specified|not_provided": 6,
    "Inborn_mitochondrial_myopathy": 5,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome": 5,
    "Perrault_syndrome": 3,
    "LARS2-related_disorder|not_provided": 3,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome_4": 2,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome|not_provided|Perrault_syndrome_4": 1,
    "Perrault_syndrome_4|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome": 1,
    "Perrault_syndrome_4|not_provided|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome": 1,
    "Perrault_syndrome_4|not_provided": 1,
    "Perrault_syndrome|not_provided|Perrault_syndrome_4": 2,
    "not_provided|Perrault_syndrome_4": 3,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|LARS2-related_disorder|not_provided": 1,
    "not_provided|LARS2-related_disorder|not_specified": 3,
    "not_provided|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome_4|not_specified": 1,
    "Perrault_syndrome_4|Perrault_syndrome": 1,
    "LARS2-related_disorder|Perrault_syndrome_4": 1,
    "not_provided|LARS2-related_disorder": 4,
    "not_specified|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|LARS2-related_disorder|Perrault_syndrome_4|not_provided": 1,
    "not_provided|Perrault_syndrome_4|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome": 2,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|not_provided": 1,
    "not_provided|Perrault_syndrome": 1,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|not_specified|not_provided|Perrault_syndrome_4": 1,
    "LARS2-related_disorder": 2,
    "LARS2-Related_Disorders|not_provided": 1,
    "not_specified|not_provided|Inborn_mitochondrial_myopathy": 1,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Rare_genetic_deafness|LARS2-related_disorder|LARS2-Related_Disorders|Inborn_genetic_diseases|Perrault_syndrome|Perrault_syndrome_4|not_provided": 1,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome_4|not_provided|not_specified": 1,
    "not_specified|not_provided|Perrault_syndrome_4|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome": 1,
    "Perrault_syndrome_4|Nonsyndromic_genetic_hearing_loss|Perrault_syndrome|not_provided": 1,
    "not_provided|Perrault_syndrome_4|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Inborn_genetic_diseases": 1,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome_4|not_specified|not_provided": 1,
    "Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|not_provided|not_specified|Perrault_syndrome_4": 1,
    "not_specified|LARS2-related_disorder|not_provided": 1,
    "LARS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome_4|not_provided": 1,
    "LARS2-related_disorder|not_specified|Perrault_syndrome_4|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Hydrops-lactic_acidosis-sideroblastic_anemia-multisystemic_failure_syndrome|Perrault_syndrome_4|not_provided": 1,
    "Perrault_syndrome_4|not_specified|not_provided|LARS2-related_disorder": 1,
    "Inborn_genetic_diseases|Perrault_syndrome_4|not_specified|not_provided": 1,
    "Hyperglycinuria": 122,
    "not_provided|Hyperglycinuria": 11,
    "Hyperglycinuria|not_provided": 10,
    "not_specified|Hyperglycinuria": 1,
    "Hyperglycinuria|not_specified|Iminoglycinuria": 2,
    "not_specified|Hyperglycinuria|Iminoglycinuria": 1,
    "Hyperglycinuria|not_specified|Hereditary_ataxia": 1,
    "not_specified|Iminoglycinuria|Hyperglycinuria|not_provided": 1,
    "not_provided|Hyperglycinuria|Iminoglycinuria": 3,
    "Hyperglycinuria|not_provided|not_specified": 1,
    "SLC6A20-related_Neurodevelopmental_Disorder|not_provided": 1,
    "SLC6A20-related_disorder": 6,
    "Hyperglycinuria|Iminoglycinuria": 10,
    "SLC6A20-related_disorder|Hyperglycinuria|Iminoglycinuria|not_provided": 1,
    "Hyperglycinuria|not_provided|SLC6A20-related_disorder": 2,
    "SLC6A20-related_disorder|Hyperglycinuria|not_provided": 2,
    "not_provided|Iminoglycinuria|Hyperglycinuria": 1,
    "SLC6A20-related_disorder|not_provided|Hyperglycinuria": 1,
    "SLC6A20-related_disorder|Hyperglycinuria": 1,
    "Hyperglycinuria|SLC6A20-related_disorder": 1,
    "Hyperglycinuria|not_specified": 1,
    "Iminoglycinuria|Hyperglycinuria": 3,
    "not_provided|Hyperglycinuria|SLC6A20-related_disorder": 1,
    "LZTFL1-related_disorder": 30,
    "Inborn_genetic_diseases|not_provided|LZTFL1-related_disorder": 2,
    "not_provided|LZTFL1-related_disorder": 6,
    "not_provided|Bardet-Biedl_syndrome_17": 6,
    "Bardet-Biedl_syndrome_17|not_provided": 7,
    "LZTFL1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_17|not_provided": 1,
    "Bardet-Biedl_syndrome_17|Bardet-Biedl_syndrome_1": 2,
    "Bardet-Biedl_syndrome_17": 17,
    "LZTFL1-related_disorder|not_provided": 11,
    "LZTFL1-related_disorder|not_provided|Bardet-Biedl_syndrome_17": 2,
    "Bardet-Biedl_syndrome_17|not_provided|Inborn_genetic_diseases|LZTFL1-related_disorder": 3,
    "Bardet-Biedl_syndrome_17|LZTFL1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|LZTFL1-related_disorder|not_provided": 1,
    "not_provided|LZTFL1-related_disorder|Bardet-Biedl_syndrome_17": 1,
    "Inborn_genetic_diseases|LZTFL1-related_disorder|not_provided|Bardet-Biedl_syndrome_17": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_17": 1,
    "Bardet-Biedl_syndrome_17|LZTFL1-related_disorder": 3,
    "LZTFL1-related_disorder|not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome_17": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_17|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_1": 42,
    "not_specified|Bardet-Biedl_syndrome_17": 1,
    "LZTFL1-related_disorder|Bardet-Biedl_syndrome_17": 1,
    "not_provided|Cataract_18": 16,
    "Cataract_18": 185,
    "Cataract_18|not_provided": 26,
    "Developmental_cataract|not_provided": 2,
    "Inborn_genetic_diseases|Cataract_18": 17,
    "not_provided|Cataract_18|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|FYCO1-related_disorder": 1,
    "FYCO1-related_disorder": 9,
    "Cataract_18|Inborn_genetic_diseases": 7,
    "Cataract_18|not_provided|not_specified": 5,
    "Cataract_18|not_specified|not_provided": 3,
    "FYCO1-related_disorder|Inborn_genetic_diseases|not_provided|Cataract_18": 1,
    "Cataract_18|FYCO1-related_disorder": 5,
    "Inborn_genetic_diseases|not_provided|Cataract_18": 3,
    "FYCO1-related_disorder|Cataract_18": 4,
    "Inborn_genetic_diseases|Cataract_18|FYCO1-related_disorder": 1,
    "not_provided|not_specified|Cataract_18": 4,
    "Cataract_18|Abnormality_of_the_eye": 1,
    "not_specified|not_provided|Cataract_18": 3,
    "Cataract_18|not_specified|Developmental_cataract": 1,
    "Inborn_genetic_diseases|FYCO1-related_disorder|Cataract_18|not_provided": 1,
    "not_provided|Cataract_18|FYCO1-related_disorder": 2,
    "Cataract_18|Inborn_genetic_diseases|FYCO1-related_disorder": 1,
    "Cataract_18|not_provided|FYCO1-related_disorder": 2,
    "not_specified|not_provided|Cataract_18|FYCO1-related_disorder": 1,
    "FYCO1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Cataract_18|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|FYCO1-related_disorder|Cataract_18": 1,
    "Cataract_18|not_provided|FYCO1-related_disorder|Inborn_genetic_diseases": 1,
    "FYCO1-related_disorder|not_provided": 1,
    "Cystic_disease_of_lung": 5,
    "Susceptibility_to_HIV_infection|CCR2-related_disorder": 1,
    "CCR2-related_disorder": 5,
    "Susceptibility_to_HIV_infection|not_specified": 1,
    "CCR5-related_disorder|CCR5_PROMOTER_POLYMORPHISM|Acquired_immunodeficiency_syndrome|_delayed_progression_to|Susceptibility_to_HIV_infection": 1,
    "not_specified|Human_immunodeficiency_virus_type_1|_increased_perinatal_transmission_of": 1,
    "CCR5-related_disorder": 5,
    "not_specified|CCR5-related_disorder": 1,
    "not_provided|West_Nile_virus|_susceptibility_to|Type_1_diabetes_mellitus_22|Hepatitis_C_virus|_susceptibility_to|Susceptibility_to_HIV_infection": 1,
    "CCR5-related_disorder|not_provided|West_Nile_virus|_susceptibility_to|Resistance_to_hepatitis_C_virus|Multiple_sclerosis_modifier_of_disease_progression|Susceptibility_to_HIV_infection": 1,
    "not_provided|CCR5_POLYMORPHISM|_ORIENTAL_2": 1,
    "CCR5_POLYMORPHISM|_ORIENTAL_1": 1,
    "not_provided|CCR5_POLYMORPHISM|_AFRICAN-AMERICAN": 1,
    "CRIPTO-related_disorder": 1,
    "not_provided|CRIPTO-related_disorder": 1,
    "Forebrain_defects": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_6": 29,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_6": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_6|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_6": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_6|not_provided": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_6|not_provided|TMIE-related_disorder|not_specified": 1,
    "Sensorineural_hearing_loss_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_6": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_6|TMIE-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_6|not_provided|not_specified": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_6|not_provided": 1,
    "not_provided|TMIE-related_disorder": 1,
    "TMIE-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_6": 1,
    "Sensorineural_hearing_loss_disorder|not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_6": 1,
    "Sensorineural_hearing_loss_disorder|not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_6|Hearing_impairment": 1,
    "not_provided|Hearing_loss|_autosomal_recessive": 17,
    "Hearing_loss|_autosomal_recessive|not_specified|not_provided": 2,
    "TMIE-related_disorder|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_6": 1,
    "TMIE-related_disorder|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_8": 6,
    "not_provided|Hypertrophic_cardiomyopathy_8": 2,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_8|Cardiomyopathy": 1,
    "MYL3-related_disorder|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_8|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy": 325,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 10,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 372,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 21,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy": 416,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 9,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_8": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 42,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 5,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_8|Cardiomyopathy|not_specified": 1,
    "MYL3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 15,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 26,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 8,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 8,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 22,
    "not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_8": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 9,
    "MYL3-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 10,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYL3-related_disorder|Cardiovascular_phenotype|Increased_left_ventricular_wall_thickness|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 7,
    "not_provided|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 46,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 54,
    "Hypertrophic_cardiomyopathy|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_8|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 5,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 35,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 7,
    "MYL3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 6,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 5,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 54,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 41,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 10,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 60,
    "Hypertrophic_cardiomyopathy|MYL3-related_disorder": 1,
    "MYL3-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_8": 1,
    "not_provided|Hypertrophic_cardiomyopathy_8|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_8": 1,
    "Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 13,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 39,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 41,
    "not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 4,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 6,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_8": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 11,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|not_provided|not_specified": 1,
    "MYL3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_8|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 35,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 5,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 4,
    "Hypertrophic_cardiomyopathy_8|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|MERRF_syndrome|Hypertrophic_cardiomyopathy": 1,
    "MYL3-related_disorder|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_8": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_8": 1,
    "Hypertrophic_cardiomyopathy_8|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_8": 1,
    "Dilated_cardiomyopathy_1U": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_8|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 66,
    "Hypertrophic_cardiomyopathy_8|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_8|not_provided": 1,
    "Hypertrophic_cardiomyopathy_8|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_8": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 6,
    "not_specified|MYL3-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 3,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 4,
    "Cardiovascular_phenotype|MYL3-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_8|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1U|Cardiovascular_phenotype": 1,
    "Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type": 11,
    "Metaphyseal_chondrodysplasia|_Jansen_type|not_provided|Chondrodysplasia_Blomstrand_type": 2,
    "Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Chondrodysplasia_Blomstrand_type": 31,
    "Chondrodysplasia_Blomstrand_type|Connective_tissue_disorder|not_provided|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|not_specified|not_provided": 1,
    "Eiken_syndrome": 3,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Inborn_genetic_diseases|not_provided|Chondrodysplasia_Blomstrand_type|PTH1R-related_disorder|Eiken_syndrome|Primary_failure_of_tooth_eruption": 1,
    "not_provided|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Inborn_genetic_diseases": 1,
    "Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|Eiken_syndrome": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|not_provided": 2,
    "Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "not_provided|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|Primary_failure_of_tooth_eruption": 1,
    "not_provided|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome": 5,
    "Chondrodysplasia_Blomstrand_type|Connective_tissue_disorder|not_provided|Metaphyseal_chondrodysplasia|_Jansen_type|Inborn_genetic_diseases|Eiken_syndrome|Primary_failure_of_tooth_eruption": 1,
    "Chondrodysplasia_Blomstrand_type|not_specified|Connective_tissue_disorder|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 1,
    "not_provided|Chondrodysplasia_Blomstrand_type": 3,
    "Inborn_genetic_diseases|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|not_provided": 1,
    "Chondrodysplasia_Blomstrand_type|not_provided|Metaphyseal_chondrodysplasia|_Jansen_type": 2,
    "Eiken_syndrome|Chondrodysplasia_Blomstrand_type|not_provided": 1,
    "Chondrodysplasia_Blomstrand_type": 4,
    "not_specified|not_provided|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "not_provided|Chondrodysplasia_Blomstrand_type|Primary_failure_of_tooth_eruption|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "Chondrodysplasia_Blomstrand_type|not_provided|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption": 1,
    "Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type": 1,
    "PTH1R-related_disorder": 3,
    "Primary_failure_of_tooth_eruption|not_provided": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type": 1,
    "Inborn_genetic_diseases|Primary_failure_of_tooth_eruption|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|not_provided": 1,
    "Primary_failure_of_tooth_eruption": 9,
    "Metaphyseal_chondrodysplasia|_Jansen_type": 9,
    "not_provided|Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Chondrodysplasia_Blomstrand_type": 2,
    "not_provided|Primary_failure_of_tooth_eruption|Eiken_syndrome|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption": 1,
    "Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 3,
    "Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Chondrodysplasia_Blomstrand_type|not_provided": 2,
    "Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|not_provided": 2,
    "Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|Eiken_syndrome|not_provided": 2,
    "Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 1,
    "Pseudohypoparathyroidism": 10,
    "Inborn_genetic_diseases|not_provided|Eiken_syndrome|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption": 1,
    "not_provided|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption": 3,
    "Primary_failure_of_tooth_eruption|Eiken_syndrome|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 2,
    "Skeletal_dysplasia|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Skeletal_dysplasia": 1,
    "Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|not_provided": 1,
    "Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided|PTH1R-related_disorder|Chondrodysplasia|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia": 1,
    "Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|not_provided|PTH1R-related_disorder": 1,
    "not_provided|Eiken_syndrome|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 1,
    "not_provided|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type": 2,
    "Inborn_genetic_diseases|not_provided|Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Chondrodysplasia_Blomstrand_type": 1,
    "not_provided|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type": 2,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome|not_provided": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|Intellectual_disability": 1,
    "not_provided|Connective_tissue_disorder|not_specified|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome": 1,
    "PTH1R-related_disorder|not_provided": 1,
    "Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|not_specified|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|PTH1R-related_disorder|Connective_tissue_disorder|not_provided|Brachydactyly_type_E1": 1,
    "Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 2,
    "Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|not_provided": 1,
    "Brachydactyly_type_E1": 1,
    "not_provided|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type": 1,
    "Inborn_genetic_diseases|Primary_failure_of_tooth_eruption|Eiken_syndrome|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "Inborn_genetic_diseases|not_provided|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "Inborn_genetic_diseases|Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|not_provided": 1,
    "Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Metaphyseal_chondrodysplasia|_Jansen_type|PTH1R-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Connective_tissue_disorder|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Eiken_syndrome|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|not_provided": 1,
    "Chondrodysplasia_Blomstrand_type|not_provided|Metaphyseal_chondrodysplasia|_Jansen_type|PTH1R-related_disorder": 1,
    "Primary_failure_of_tooth_eruption|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|not_provided": 1,
    "Metaphyseal_chondrodysplasia|_Jansen_type|Chondrodysplasia_Blomstrand_type|Primary_failure_of_tooth_eruption|Eiken_syndrome": 1,
    "not_provided|PTH1R-related_disorder|Connective_tissue_disorder": 1,
    "not_provided|Metaphyseal_chondrodysplasia|_Jansen_type|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome": 1,
    "Inborn_genetic_diseases|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Eiken_syndrome|Metaphyseal_chondrodysplasia|_Jansen_type|not_provided": 1,
    "not_provided|Eiken_syndrome|Primary_failure_of_tooth_eruption|Chondrodysplasia_Blomstrand_type|Metaphyseal_chondrodysplasia|_Jansen_type|Inborn_genetic_diseases": 1,
    "Chondrodysplasia_Blomstrand_type|Connective_tissue_disorder|Metaphyseal_chondrodysplasia|_Jansen_type": 1,
    "not_provided|Chondrodysplasia|Metaphyseal_chondrodysplasia": 1,
    "Gray_platelet_syndrome": 186,
    "NBEAL2-related_disorder|not_provided|Gray_platelet_syndrome": 2,
    "NBEAL2-related_disorder": 30,
    "not_provided|Gray_platelet_syndrome|NBEAL2-related_disorder": 1,
    "NBEAL2-related_disorder|Gray_platelet_syndrome": 5,
    "not_specified|not_provided|Gray_platelet_syndrome": 4,
    "Gray_platelet_syndrome|not_provided": 15,
    "Inborn_genetic_diseases|Gray_platelet_syndrome": 18,
    "Gray_platelet_syndrome|not_provided|NBEAL2-related_disorder": 3,
    "not_provided|not_specified|Gray_platelet_syndrome": 6,
    "NBEAL2-related_disorder|not_specified|not_provided|Gray_platelet_syndrome": 1,
    "Inborn_genetic_diseases|Gray_platelet_syndrome|not_provided": 2,
    "Gray_platelet_syndrome|not_provided|not_specified": 1,
    "NBEAL2-related_disorder|not_provided": 5,
    "not_specified|Gray_platelet_syndrome|not_provided": 8,
    "not_specified|Inborn_genetic_diseases|Gray_platelet_syndrome": 1,
    "NBEAL2-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Gray_platelet_syndrome": 2,
    "Gray_platelet_syndrome|Inborn_genetic_diseases|NBEAL2-related_disorder": 1,
    "Gray_platelet_syndrome|not_specified": 2,
    "Gray_platelet_syndrome|Inborn_genetic_diseases": 10,
    "not_provided|Gray_platelet_syndrome|not_specified|NBEAL2-related_disorder": 1,
    "Inborn_genetic_diseases|Abnormal_bleeding|Thrombocytopenia|NBEAL2-related_disorder|not_specified|Gray_platelet_syndrome|not_provided": 1,
    "NBEAL2-related_disorder|Inborn_genetic_diseases": 1,
    "NBEAL2-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|NBEAL2-related_disorder": 3,
    "Thrombocytopenia|Abnormal_bleeding|Inborn_genetic_diseases|Gray_platelet_syndrome": 1,
    "not_provided|Gray_platelet_syndrome": 6,
    "NBEAL2-related_disorder|Gray_platelet_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Gray_platelet_syndrome": 2,
    "NBEAL2-related_disorder|not_provided|not_specified|Gray_platelet_syndrome": 1,
    "not_provided|Gray_platelet_syndrome|not_specified": 5,
    "not_provided|NBEAL2-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Gray_platelet_syndrome|Abnormal_bleeding|Thrombocytopenia": 1,
    "not_specified|Gray_platelet_syndrome": 3,
    "not_provided|NBEAL2-related_disorder|Gray_platelet_syndrome": 1,
    "Abnormal_bleeding|Thrombocytopenia": 29,
    "not_specified|Gray_platelet_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|NBEAL2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NBEAL2-related_disorder|Gray_platelet_syndrome|not_specified": 1,
    "not_specified|NBEAL2-related_disorder|Abnormal_bleeding|Thrombocytopenia|not_provided|Gray_platelet_syndrome": 1,
    "not_provided|Gray_platelet_syndrome|NBEAL2-related_disorder|not_specified": 1,
    "NBEAL2-related_disorder|Gray_platelet_syndrome|not_provided": 1,
    "Luscan-Lumish_syndrome": 575,
    "Inborn_genetic_diseases|not_specified|Luscan-Lumish_syndrome": 1,
    "Luscan-Lumish_syndrome|not_provided": 36,
    "Inborn_genetic_diseases|Luscan-Lumish_syndrome": 19,
    "Luscan-Lumish_syndrome|Inborn_genetic_diseases": 29,
    "Luscan-Lumish_syndrome|SETD2-related_disorder|not_provided": 4,
    "Luscan-Lumish_syndrome|not_specified": 11,
    "SETD2-related_disorder|Luscan-Lumish_syndrome": 16,
    "Luscan-Lumish_syndrome|not_specified|not_provided": 5,
    "not_provided|Luscan-Lumish_syndrome": 26,
    "SETD2-related_disorder|Inborn_genetic_diseases|Luscan-Lumish_syndrome|not_provided": 2,
    "SETD2-related_disorder": 26,
    "Inborn_genetic_diseases|not_provided|Luscan-Lumish_syndrome|not_specified": 1,
    "not_provided|Luscan-Lumish_syndrome|not_specified": 4,
    "not_specified|Luscan-Lumish_syndrome|not_provided": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Luscan-Lumish_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Luscan-Lumish_syndrome": 6,
    "Inborn_genetic_diseases|not_provided|Luscan-Lumish_syndrome": 3,
    "not_provided|SETD2-related_disorder|Luscan-Lumish_syndrome": 4,
    "Luscan-Lumish_syndrome|SETD2-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Luscan-Lumish_syndrome|not_provided|not_specified": 2,
    "Luscan-Lumish_syndrome|not_specified|SETD2-related_disorder": 2,
    "Luscan-Lumish_syndrome|SETD2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Luscan-Lumish_syndrome|not_specified|Inborn_genetic_diseases": 2,
    "Luscan-Lumish_syndrome|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70": 4,
    "Luscan-Lumish_syndrome|not_provided|Intellectual_developmental_disorder|_autosomal_dominant_70": 1,
    "Rabin-Pappas_syndrome|SETD2-related_disorder|Luscan-Lumish_syndrome|Corpus_callosum|_agenesis_of|Cerebellar_vermis_hypoplasia|not_provided|Congenital_cerebellar_hypoplasia|SETD2_associated_neurodevelopmental_disorder_with_multiple_congenital_anomalies|Inborn_genetic_diseases": 1,
    "Wee1_Inhibitor_response": 1,
    "Dandy-Walker_syndrome|Luscan-Lumish_syndrome|Genetic_syndrome_with_a_Dandy-Walker_malformation_as_major_feature|Ventriculomegaly": 1,
    "not_provided|SETD2-related_disorder|not_specified|Luscan-Lumish_syndrome": 2,
    "Intellectual_developmental_disorder|_autosomal_dominant_70": 3,
    "SETD2-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Luscan-Lumish_syndrome": 1,
    "not_specified|SETD2-related_disorder": 1,
    "Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70|Luscan-Lumish_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Luscan-Lumish_syndrome|not_provided": 2,
    "Acute_megakaryoblastic_leukemia_without_down_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|SETD2-related_disorder|Luscan-Lumish_syndrome": 1,
    "SETD2-related_disorder|Luscan-Lumish_syndrome|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70|not_provided": 1,
    "not_specified|not_provided|Luscan-Lumish_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Luscan-Lumish_syndrome": 2,
    "not_provided|SETD2-related_disorder|Inborn_genetic_diseases|Luscan-Lumish_syndrome": 1,
    "Luscan-Lumish_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "Intellectual_disability|not_provided|Luscan-Lumish_syndrome": 1,
    "SETD2-related_disorder|Luscan-Lumish_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Luscan-Lumish_syndrome|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70|SETD2-related_disorder": 1,
    "SETD2-related_disorder|Luscan-Lumish_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|SETD2-related_disorder|Luscan-Lumish_syndrome": 1,
    "Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70|Luscan-Lumish_syndrome": 1,
    "not_provided|SETD2-related_disorder": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Luscan-Lumish_syndrome|SETD2-related_disorder": 1,
    "Luscan-Lumish_syndrome|SETD2-related_disorder": 3,
    "not_provided|not_specified|Luscan-Lumish_syndrome": 3,
    "SETD2-related_disorder|Luscan-Lumish_syndrome|not_specified|not_provided": 5,
    "Luscan-Lumish_syndrome|SETD2-related_disorder|not_specified": 1,
    "Rabin-Pappas_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Luscan-Lumish_syndrome": 3,
    "Luscan-Lumish_syndrome|Autism|not_provided|Inborn_genetic_diseases": 1,
    "Luscan-Lumish_syndrome|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Luscan-Lumish_syndrome|SETD2-related_disorder": 1,
    "not_provided|Luscan-Lumish_syndrome|Inborn_genetic_diseases": 1,
    "Luscan-Lumish_syndrome|not_provided|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70": 1,
    "See_cases|Luscan-Lumish_syndrome": 1,
    "Hereditary_ataxia|Luscan-Lumish_syndrome|Inborn_genetic_diseases": 1,
    "Luscan-Lumish_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70": 1,
    "Luscan-Lumish_syndrome|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70|SETD2-related_disorder|Inborn_genetic_diseases": 1,
    "Luscan-Lumish_syndrome|Inborn_genetic_diseases|SETD2-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_70|not_provided": 1,
    "not_provided|Luscan-Lumish_syndrome|Rabin-Pappas_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_70": 1,
    "SETD2-related_neurodevelopmental_disorder_without_or_with_macrocephaly/overgrowth|Luscan-Lumish_syndrome": 1,
    "Luscan-Lumish_syndrome|Intellectual_disability": 1,
    "not_provided|SETD2-related_disorder|not_specified|Inborn_genetic_diseases|Luscan-Lumish_syndrome": 1,
    "PTPN23-related_disorder|not_provided": 14,
    "not_provided|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 6,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 23,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|Inborn_genetic_diseases|not_provided": 1,
    "Brain_atrophy|Global_developmental_delay|not_provided|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided": 15,
    "Inborn_genetic_diseases|PTPN23-related_disorder|not_provided": 2,
    "PTPN23-related_disorder|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided": 2,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided|PTPN23-related_disorder": 2,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided|Brain_atrophy|Global_developmental_delay": 1,
    "not_provided|PTPN23-related_disorder": 8,
    "PTPN23-related_disorder|not_provided|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 2,
    "Inborn_genetic_diseases|not_provided|PTPN23-related_disorder": 2,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|PTPN23-related_disorder": 1,
    "Brain_atrophy|Global_developmental_delay|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 3,
    "not_specified|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided": 1,
    "Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided|Inborn_genetic_diseases": 2,
    "Global_developmental_delay|Brain_atrophy|not_provided": 1,
    "Brain_atrophy|Global_developmental_delay|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 1,
    "Global_developmental_delay|Brain_atrophy|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|Neurodevelopmental_disorder|not_provided": 1,
    "PTPN23-related_disorder": 3,
    "Global_developmental_delay|Brain_atrophy|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided": 1,
    "PTPN23-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PTPN23-related_disorder|Inborn_genetic_diseases": 2,
    "Global_developmental_delay|Brain_atrophy|not_provided|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 1,
    "PTPN23-related_neurodevelopmental_disorder": 1,
    "PTPN23-related_disorder|Brain_atrophy|Global_developmental_delay|not_provided|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Brain_atrophy|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity|not_provided": 1,
    "not_provided|Global_developmental_delay|Brain_atrophy|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 1,
    "Global_developmental_delay|Seizure|Brain_atrophy|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 1,
    "Brain_atrophy|Global_developmental_delay|not_provided|Neurodevelopmental_disorder_and_structural_brain_anomalies_with_or_without_seizures_and_spasticity": 1,
    "SMARCC1-related_disorder": 15,
    "SMARCC1-associated_developmental_dysgenesis_syndrome": 2,
    "Congenital_hydrocephalus|Hydrocephalus|_congenital|_5|_susceptibility_to": 2,
    "SMARCC1-related_disorder|Inborn_genetic_diseases": 1,
    "Hydrocephalus|_congenital|_5|_susceptibility_to": 3,
    "not_provided|SMARCC1-related_disorder": 1,
    "not_provided|Hydrocephalus|_congenital|_5|_susceptibility_to": 2,
    "SMARCC1-related_disorder|not_provided": 2,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language": 37,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|not_provided": 3,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|DHX30-related_disorder|Inborn_genetic_diseases": 1,
    "DHX30-related_disorder": 13,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|not_specified": 1,
    "not_provided|Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language": 1,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|not_provided|Seizure|Short_stature|Microcephaly|Strabismus|Oculomotor_apraxia|Unsteady_gait": 1,
    "Abnormal_cerebral_white_matter_morphology|Autism|Intellectual_disability|Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|Global_developmental_delay|Strabismus|Hearing_impairment|Axial_hypotonia|Sleep_abnormality|Delayed_speech_and_language_development|Microcephaly": 1,
    "Autism|_susceptiblity_to": 5,
    "not_provided|Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|Inborn_genetic_diseases": 2,
    "not_provided|DHX30-related_disorder": 3,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|not_provided|Hirsutism|Short_stature|Failure_to_thrive|EEG_abnormality|Generalized_hypotonia|Global_developmental_delay|Microcephaly|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_severe_motor_impairment_and_absent_language": 2,
    "MAP4-related_disorder|not_provided": 4,
    "MAP4-related_disorder": 27,
    "not_provided|MAP4-related_disorder": 2,
    "Kleine-Levin_syndrome": 2,
    "Kleine-Levin_syndrome|not_specified": 3,
    "not_specified|Autosomal_dominant_polycystic_liver_disease": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_specified": 2,
    "ZNF589-related_disorder": 3,
    "ZNF589-related_disorder|not_provided": 2,
    "ZNF589-related_disorder|not_specified": 1,
    "PLXNB1-related_disorder": 38,
    "not_provided|PLXNB1-related_disorder": 7,
    "not_specified|PLXNB1-related_disorder": 2,
    "PLXNB1-related_disorder|not_provided": 6,
    "not_specified|not_provided|ATRIP-related_disorder": 2,
    "Seckel_syndrome|Microcephalic_Primordial_Dwarfism_with_immunodeficiency": 1,
    "Microcephalic_Primordial_Dwarfism_with_immunodeficiency": 1,
    "ATRIP-related_disorder|not_provided|not_specified": 1,
    "not_specified|ATRIP-related_disorder|not_provided": 1,
    "ATRIP-related_disorder|not_provided": 2,
    "ATRIP-related_disorder|not_specified|not_provided": 1,
    "Aicardi_Goutieres_syndrome|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 7,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1": 2,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided|Aicardi_Goutieres_syndrome": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 2,
    "Aicardi_Goutieres_syndrome|not_provided|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "Aicardi-Goutieres_syndrome_1": 18,
    "TREX1-related_disorder|Intellectual_disability": 1,
    "TREX1-related_disorder": 6,
    "not_provided|Aicardi-Goutieres_syndrome_1|TREX1-related_disorder": 1,
    "Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1": 47,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 140,
    "not_provided|Systemic_lupus_erythematosus|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Inborn_genetic_diseases": 3,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1": 135,
    "TREX1-related_disorder|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1": 2,
    "not_provided|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|TREX1-related_disorder": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1": 36,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 3,
    "Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|TREX1-related_disorder|not_specified": 1,
    "Chilblain_lupus|not_provided|Aicardi-Goutieres_syndrome_1|_autosomal_dominant|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1": 1,
    "TREX1-related_disorder|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided": 1,
    "Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 18,
    "TREX1-related_disorder|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "not_provided|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1": 3,
    "not_provided|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified": 2,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided": 6,
    "not_provided|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1": 2,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1": 1,
    "Systemic_lupus_erythematosus|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|TREX1-related_disorder|not_provided": 1,
    "TREX1-related_disorder|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1": 2,
    "not_provided|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|See_cases": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|not_provided": 1,
    "Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Inborn_genetic_diseases": 2,
    "Retinal_dystrophy|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1": 1,
    "Aicardi-Goutieres_syndrome_1|See_cases|not_provided": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided|TREX1-related_disorder|not_specified": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Inborn_genetic_diseases": 6,
    "not_specified|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 3,
    "not_provided|Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified": 1,
    "not_specified|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|not_provided": 1,
    "Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided": 1,
    "Chilblain_lupus_1|Systemic_lupus_erythematosus|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided": 1,
    "not_specified|not_provided|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|not_provided|Systemic_lupus_erythematosus|TREX1-related_disorder": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|not_specified": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|Chilblain_lupus_1|not_provided": 1,
    "not_provided|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Systemic_lupus_erythematosus|Chilblain_lupus_1": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|Chilblain_lupus_1": 2,
    "not_provided|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Inborn_genetic_diseases": 1,
    "Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|TREX1-related_disorder|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|TREX1-related_disorder": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|not_provided|TREX1-related_disorder": 1,
    "Inborn_genetic_diseases|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|TREX1-related_disorder|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|not_provided|Systemic_lupus_erythematosus|_susceptibility_to": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided|Chilblain_lupus_1": 1,
    "not_provided|Chilblain_lupus|Systemic_lupus_erythematosus|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1": 1,
    "Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|TREX1-related_disorder": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|not_specified": 2,
    "not_provided|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 5,
    "not_provided|Aicardi-Goutieres_syndrome_1": 3,
    "TREX1-related_disorder|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 2,
    "not_specified|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Inborn_genetic_diseases": 3,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|not_provided": 1,
    "not_specified|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|not_provided": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|not_provided": 3,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "TREX1-related_disorder|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|not_provided": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|TREX1-related_disorder": 1,
    "not_provided|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Systemic_lupus_erythematosus|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|not_specified": 1,
    "not_specified|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1": 2,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified|not_provided": 2,
    "Chilblain_lupus_1": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided|not_specified": 1,
    "not_provided|Systemic_lupus_erythematosus|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|_autosomal_dominant": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|TREX1-related_disorder|Inborn_genetic_diseases|not_provided|Systemic_lupus_erythematosus": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified": 2,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Systemic_lupus_erythematosus|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "TREX1-related_disorder|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "not_specified|not_provided|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|TREX1-related_disorder|not_provided|not_specified": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|not_provided": 1,
    "not_provided|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1": 2,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 3,
    "not_provided|not_specified|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 2,
    "Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified|TREX1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1|not_provided": 1,
    "Inborn_genetic_diseases|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1": 1,
    "Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|Chilblain_lupus_1|TREX1-related_disorder|Aicardi_Goutieres_syndrome|not_specified|not_provided": 1,
    "Retinal_dystrophy|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Chilblain_lupus_1": 1,
    "not_provided|TREX1-related_disorder|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "not_provided|Thrombotic_microangiopathy": 1,
    "not_provided|Chilblain_lupus_1|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations": 1,
    "Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Systemic_lupus_erythematosus|TREX1-related_disorder|Aicardi_Goutieres_syndrome|not_provided": 1,
    "Aicardi_Goutieres_syndrome|not_provided|not_specified|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Vascular_dementia|Aicardi-Goutieres_syndrome_1|Chilblain_lupus_1|Systemic_lupus_erythematosus|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_specified|not_provided|TREX1-related_disorder": 1,
    "Chilblain_lupus_1|Systemic_lupus_erythematosus|Aicardi-Goutieres_syndrome_1|Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|not_provided|TREX1-related_disorder|Retinal_dystrophy": 1,
    "Retinal_vasculopathy_with_cerebral_leukoencephalopathy_and_systemic_manifestations|Aicardi_Goutieres_syndrome|not_provided": 1,
    "Epidermolysis_bullosa_dystrophica": 243,
    "Epidermolysis_bullosa_dystrophica|not_provided": 95,
    "not_provided|Epidermolysis_bullosa_dystrophica": 147,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 53,
    "COL7A1-related_disorder|not_provided": 16,
    "not_provided|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 8,
    "not_provided|Epidermolysis_bullosa_pruriginosa": 1,
    "not_specified|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 2,
    "not_provided|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|COL7A1-related_disorder": 1,
    "Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|not_specified|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided": 3,
    "not_provided|COL7A1-related_disorder": 17,
    "Epidermolysis_bullosa_dystrophica|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa": 31,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 7,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica": 5,
    "Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 42,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided": 16,
    "COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa|_pretibial|_autosomal_recessive|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|COL7A1-related_disorder|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 14,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8": 5,
    "COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa": 108,
    "Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|Epidermolysis_bullosa_dystrophica|Inborn_genetic_diseases|COL7A1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|COL7A1-related_disorder": 2,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 5,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided": 2,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|not_specified|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn": 1,
    "COL7A1-related_disorder": 18,
    "COL7A1-related_disorder|not_provided|Recessive_dystrophic_epidermolysis_bullosa": 2,
    "Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|not_provided": 7,
    "not_provided|Epidermolysis_bullosa_dystrophica|Inborn_genetic_diseases": 11,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa": 23,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 3,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_dystrophica|not_provided|COL7A1-related_disorder": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided": 38,
    "not_specified|Epidermolysis_bullosa_dystrophica|not_provided": 3,
    "not_provided|Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder": 3,
    "Epidermolysis_bullosa_pruriginosa": 7,
    "Transient_bullous_dermolysis_of_the_newborn": 8,
    "not_provided|not_specified|Epidermolysis_bullosa_dystrophica": 3,
    "Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa": 2,
    "not_provided|COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided": 1,
    "not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica": 6,
    "Epidermolysis_bullosa_pruriginosa|not_provided|COL7A1-related_disorder": 1,
    "Epidermolysis_bullosa_pruriginosa|Finger_syndactyly|Toe_syndactyly|Short_stature|Palmoplantar_blistering": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|COL7A1-related_disorder": 3,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 3,
    "not_provided|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 4,
    "Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 2,
    "Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 5,
    "Pretibial_dystrophic_epidermolysis_bullosa": 2,
    "not_provided|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Pretibial_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8": 1,
    "Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided|Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "COL7A1-related_disorder|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided|Epidermolysis_bullosa_pruriginosa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|Epidermolysis_bullosa_dystrophica": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Recessive_dystrophic_epidermolysis_bullosa|COL7A1-related_disorder|not_provided": 1,
    "not_provided|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 4,
    "not_specified|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8": 5,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 9,
    "COL7A1-related_disorder|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Generalized_dominant_dystrophic_epidermolysis_bullosa": 10,
    "Recessive_dystrophic_epidermolysis_bullosa|not_specified": 2,
    "not_provided|Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa": 4,
    "not_provided|COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "not_provided|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn": 4,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|_autosomal_recessive|_localisata_variant|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_pruriginosa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_dystrophica|Inborn_genetic_diseases": 4,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 3,
    "Recessive_dystrophic_epidermolysis_bullosa|COL7A1-related_disorder|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 8,
    "Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|not_provided": 2,
    "not_specified|not_provided|Recessive_dystrophic_epidermolysis_bullosa": 2,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|Nonsyndromic_congenital_nail_disorder_8|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 2,
    "Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|COL7A1-related_disorder": 1,
    "not_specified|not_provided|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|Transient_bullous_dermolysis_of_the_newborn": 1,
    "not_specified|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Epidermolysis_bullosa_pruriginosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn": 1,
    "not_specified|not_provided|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8": 1,
    "not_specified|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 4,
    "not_provided|Epidermolysis_bullosa_pruriginosa|_autosomal_dominant": 2,
    "Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_pruriginosa|_autosomal_dominant|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8": 1,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn": 1,
    "Inborn_genetic_diseases|not_provided|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Pretibial_dystrophic_epidermolysis_bullosa|not_provided|COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa": 1,
    "Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|not_specified": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_dystrophica": 7,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided": 4,
    "COL7A1-related_disorder|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|See_cases": 1,
    "Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|COL7A1-related_disorder": 1,
    "not_provided|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|not_provided|Epidermolysis_bullosa_dystrophica|Abnormality_of_the_skin|COL7A1-related_disorder|See_cases": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder|not_provided": 2,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica": 3,
    "Inborn_genetic_diseases|not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa": 4,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|not_specified|Epidermolysis_bullosa_dystrophica": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Abnormality_of_the_skin|not_provided": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 3,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 6,
    "Pretibial_dystrophic_epidermolysis_bullosa|not_provided|COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_pruriginosa|_autosomal_dominant": 1,
    "COL7A1-related_disorder|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Hyperpigmentation_of_the_skin|Abnormal_blistering_of_the_skin|Nail_dystrophy|Short_stature|Failure_to_thrive|Alopecia_of_scalp|Abnormality_of_the_dentition|Microcephaly|Distal_muscle_weakness|Scarring_alopecia_of_scalp|Scarring|Decreased_body_weight|EMG_abnormality|Abnormal_dental_enamel_morphology": 1,
    "COL7A1-related_disorder|not_provided|Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Duane_retraction_syndrome|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_dystrophica|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|not_provided": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "Transient_bullous_dermolysis_of_the_newborn|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin": 1,
    "Epidermolysis_bullosa_dystrophica|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided": 2,
    "Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|not_provided": 1,
    "not_provided|Epidermolysis_bullosa": 3,
    "COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "COL7A1-related_disorder|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_specified": 1,
    "Epidermolysis_bullosa_dystrophica|not_specified|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa": 5,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|COL7A1-related_disorder": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|_autosomal_recessive|_localisata_variant|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 3,
    "Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|not_provided": 1,
    "COL7A1-related_disorder|not_specified|not_provided|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|COL7A1-related_disorder|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "Abnormal_blistering_of_the_skin": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder": 1,
    "Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|Epidermolysis_bullosa_pruriginosa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Recessive_dystrophic_epidermolysis_bullosa": 2,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 2,
    "Epidermolysis_bullosa_dystrophica|not_specified": 2,
    "Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|not_specified": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "COL7A1-related_disorder|not_specified|not_provided": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "COL7A1-related_disorder|not_provided|Epidermolysis_bullosa_dystrophica": 8,
    "Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|not_provided|COL7A1-related_disorder": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa|_pretibial|_autosomal_recessive": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|COL7A1-related_disorder|not_specified|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa": 3,
    "Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "COL7A1-related_disorder|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_pruriginosa|not_specified": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder|not_specified": 1,
    "not_provided|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "COL7A1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|not_provided|COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 1,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|not_provided": 5,
    "Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "Epidermolysis_bullosa|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_specified": 2,
    "not_provided|COL7A1-related_epidermolysis_bullosa": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|not_provided|not_specified": 1,
    "COL7A1-related_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder|not_specified|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn": 1,
    "Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|not_provided|Epidermolysis_bullosa_dystrophica": 3,
    "not_provided|COL7A1-related_disorder|not_specified|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_dystrophica|Transient_bullous_dermolysis_of_the_newborn": 2,
    "not_specified|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa": 1,
    "Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder|not_provided": 1,
    "not_provided|Pretibial_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Inborn_genetic_diseases|Recessive_dystrophic_epidermolysis_bullosa|not_provided|Transient_bullous_dermolysis_of_the_newborn|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin": 1,
    "Epidermolysis_bullosa_dystrophica|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|not_specified|Inborn_genetic_diseases": 1,
    "COL7A1-related_disorder|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica": 1,
    "Transient_bullous_dermolysis_of_the_newborn|not_provided": 2,
    "COL7A1-related_disorder|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "Epidermolysis_bullosa_dystrophica|_autosomal_recessive|_localisata_variant|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|not_provided|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Inborn_genetic_diseases": 4,
    "not_provided|Transient_bullous_dermolysis_of_the_newborn": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder": 1,
    "not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|not_specified|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|not_specified|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica|not_specified|not_provided|COL7A1-related_disorder": 1,
    "not_provided|Amelogenesis_imperfecta_type_1": 1,
    "not_provided|COL7A1-related_disorder|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_dystrophica|Amelogenesis_imperfecta_type_1|COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 3,
    "not_provided|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|COL7A1-related_disorder": 1,
    "COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_dystrophica": 4,
    "Inborn_genetic_diseases|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|not_specified": 2,
    "Epidermolysis_bullosa_dystrophica|not_provided|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_dystrophica|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "COL7A1-related_disorder|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "not_provided|COL7A1-related_disorder|not_specified": 1,
    "Epidermolysis_bullosa_pruriginosa|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Amelogenesis_imperfecta_type_1": 1,
    "Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_dystrophica|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Palmoplantar_blistering|Skin_fragility_with_non-scarring_blistering": 1,
    "COL7A1-related_disorder|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Finger_syndactyly|Palmoplantar_blistering|Short_stature|Toe_syndactyly|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Abnormal_blistering_of_the_skin|Skin_erosion|Nail_dystrophy|Abnormality_of_the_skin|Anonychia": 1,
    "not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Nonsyndromic_congenital_nail_disorder_8|not_provided": 1,
    "not_provided|COL7A1-related_disorder|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 2,
    "not_provided|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica|not_specified|not_provided": 1,
    "not_provided|Hepatoblastoma": 2,
    "COL7A1-related_disorder|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Epidermolysis_bullosa_dystrophica|not_provided|See_cases": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica|COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Pretibial_dystrophic_epidermolysis_bullosa": 1,
    "Inborn_genetic_diseases|not_specified|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica": 1,
    "not_specified|not_provided|Ichthyosis|Epidermolytic_ichthyosis|Epidermal_nevus|Abnormality_of_the_thyroid_gland": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Hepatoblastoma": 1,
    "not_provided|COL7A1-related_disorder|Inborn_genetic_diseases": 2,
    "Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Transient_bullous_dermolysis_of_the_newborn|not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|COL7A1-related_disorder": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Pretibial_dystrophic_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Microcephaly|Abnormality_of_the_dentition|Scarring_alopecia_of_scalp|Short_stature|Distal_muscle_weakness|Abnormal_dental_enamel_morphology|Decreased_body_weight|EMG_abnormality|Hyperpigmentation_of_the_skin|Nail_dystrophy|Failure_to_thrive|Alopecia_of_scalp|Scarring|Abnormal_blistering_of_the_skin": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa": 1,
    "COL7A1-related_disorder|not_provided|Epidermolysis_bullosa_dystrophica|Pretibial_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "COL7A1-related_disorder|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica": 1,
    "COL7A1-related_disorder|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa_dystrophica|Epidermolysis_bullosa_dystrophica|_autosomal_recessive|_localisata_variant|Epidermolysis_bullosa_pruriginosa|_autosomal_recessive|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive|Anonychia|Abnormality_of_the_skin|Nail_dystrophy|Skin_erosion": 1,
    "not_provided|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_pruriginosa|Epidermolysis_bullosa_dystrophica": 1,
    "Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Epidermolysis_bullosa_dystrophica|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_dystrophica|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Generalized_dominant_dystrophic_epidermolysis_bullosa": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Epidermolysis_bullosa|_pretibial|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "not_specified|Nonsyndromic_congenital_nail_disorder_8|Recessive_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Transient_bullous_dermolysis_of_the_newborn|Pretibial_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Generalized_dominant_dystrophic_epidermolysis_bullosa|Recessive_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Epidermolysis_bullosa_pruriginosa|Epidermolysis_bullosa_dystrophica": 1,
    "Epidermolysis_bullosa_dystrophica|not_provided|Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_dystrophica_inversa|_autosomal_recessive": 1,
    "Recessive_dystrophic_epidermolysis_bullosa|Epidermolysis_bullosa_pruriginosa|Nonsyndromic_congenital_nail_disorder_8|Pretibial_dystrophic_epidermolysis_bullosa|Transient_bullous_dermolysis_of_the_newborn|Dominant_dystrophic_epidermolysis_bullosa_with_absence_of_skin|Generalized_dominant_dystrophic_epidermolysis_bullosa|not_provided": 1,
    "Parkinsonism_with_polyneuropathy": 9,
    "UQCRC1-related_disorder": 2,
    "Parkinsonism_with_polyneuropathy|not_specified": 1,
    "not_specified|Parkinsonism_with_polyneuropathy": 1,
    "CELSR3-related_disorder": 32,
    "CELSR3-related_disorder|not_provided": 2,
    "CELSR3-related_disorder|Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 1,
    "Hypertrophic_cardiomyopathy|Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 1,
    "Tourette_syndrome": 101,
    "not_specified|Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 1,
    "not_provided|Tourette_syndrome": 6,
    "CELSR3-related_disorder|not_specified": 1,
    "Carnitine_acylcarnitine_translocase_deficiency": 242,
    "SLC25A20-related_disorder": 3,
    "SLC25A20-related_disorder|Carnitine_acylcarnitine_translocase_deficiency": 3,
    "Inborn_genetic_diseases|Carnitine_acylcarnitine_translocase_deficiency": 2,
    "not_specified|Carnitine_acylcarnitine_translocase_deficiency": 4,
    "not_provided|Carnitine_acylcarnitine_translocase_deficiency": 9,
    "not_provided|Carnitine_acylcarnitine_translocase_deficiency|not_specified": 1,
    "SLC25A20-related_disorder|not_specified|not_provided|Carnitine_acylcarnitine_translocase_deficiency": 1,
    "Carnitine_acylcarnitine_translocase_deficiency|not_provided": 8,
    "not_specified|not_provided|Carnitine_acylcarnitine_translocase_deficiency": 2,
    "Carnitine_acylcarnitine_translocase_deficiency|not_specified": 3,
    "Carnitine_acylcarnitine_translocase_deficiency|Inborn_genetic_diseases": 6,
    "not_specified|Carnitine_acylcarnitine_translocase_deficiency|Inborn_genetic_diseases": 1,
    "Carnitine_acylcarnitine_translocase_deficiency|SLC25A20-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Carnitine_acylcarnitine_translocase_deficiency": 1,
    "Carnitine_acylcarnitine_translocase_deficiency|not_provided|SLC25A20-related_disorder": 2,
    "Carnitine_acylcarnitine_translocase_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "Carnitine_acylcarnitine_translocase_deficiency|See_cases": 1,
    "Hypotonia|_hypoventilation|_impaired_intellectual_development|_dysautonomia|_epilepsy|_and_eye_abnormalities|Intellectual_disability": 2,
    "Hypotonia|_hypoventilation|_impaired_intellectual_development|_dysautonomia|_epilepsy|_and_eye_abnormalities": 10,
    "P4HTM-related_disorder": 1,
    "not_provided|P4HTM-related_disorder": 1,
    "P4HTM-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Poirier-Bienvenu_neurodevelopmental_syndrome": 48,
    "Developmental_and_epileptic_encephalopathy|_86|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_86": 3,
    "DALRD3-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_18|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_18|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_18": 9,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 2,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_18|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_18|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_18": 1,
    "NDUFAF3-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_18|Inborn_genetic_diseases": 1,
    "IMPDH2-related_disorder": 2,
    "IMPDH2-related_disorder|not_provided": 2,
    "IMPDH2_enzyme_activity|_variation_in": 1,
    "IMPDH2-associated_neurodevelopmental_disorder": 1,
    "IMPDH2-related_neurodevelopmental_condition|not_provided": 1,
    "Ververi-Brady_syndrome": 57,
    "QRICH1-related_disorder": 12,
    "QRICH1-related_disorder|not_provided": 1,
    "Intellectual_disability|not_provided|Ververi-Brady_syndrome": 1,
    "Ververi-Brady_syndrome|Intellectual_disability|_mild": 1,
    "not_provided|Ververi-Brady_syndrome": 5,
    "Ververi-Brady_syndrome|not_provided": 6,
    "not_provided|QRICH1-related_disorder": 1,
    "Inborn_genetic_diseases|Ververi-Brady_syndrome": 1,
    "Ververi-Brady_syndrome|not_specified": 1,
    "Ververi-Brady_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Ververi-Brady_syndrome|Intellectual_disability": 2,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 678,
    "not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 29,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided": 43,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 19,
    "Inborn_genetic_diseases|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided": 12,
    "not_provided|Inborn_genetic_diseases|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 4,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|Inborn_genetic_diseases": 16,
    "not_specified|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 13,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_specified": 28,
    "QARS1-related_disorder|not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|Inborn_genetic_diseases": 1,
    "QARS1-related_disorder|not_specified|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 4,
    "not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_specified": 3,
    "not_specified|not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 1,
    "QARS1-related_disorder|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 3,
    "not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|QARS1-related_disorder": 3,
    "Inborn_genetic_diseases|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Microcephaly|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 1,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_43": 1,
    "QARS1-related_disorder|not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome": 1,
    "QARS1-related_disorder": 1,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided|not_specified": 2,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided|Inborn_genetic_diseases": 6,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided|QARS1-related_disorder": 1,
    "Microcephaly|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided": 1,
    "QARS1-related_disorder|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_provided": 4,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_specified|not_provided|QARS1-related_disorder": 1,
    "Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_specified|not_provided": 2,
    "not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|See_cases": 1,
    "QARS1-related_disorder|not_provided|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_specified": 1,
    "See_cases|Diffuse_cerebral_and_cerebellar_atrophy_-_intractable_seizures_-_progressive_microcephaly_syndrome|not_specified|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 304,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 484,
    "not_provided|Inborn_genetic_diseases|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 2,
    "LAMB2-related_infantile-onset_nephrotic_syndrome": 10,
    "not_provided|Focal_segmental_glomerulosclerosis|LAMB2-related_infantile-onset_nephrotic_syndrome|not_specified|Pierson_syndrome": 1,
    "Pierson_syndrome": 14,
    "Pierson_syndrome|not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|Inborn_genetic_diseases": 21,
    "LAMB2-related_disorder": 10,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_specified|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided|LAMB2-related_disorder": 2,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|LAMB2-related_disorder": 7,
    "Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 39,
    "Pierson_syndrome|not_specified|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided|LAMB2-related_disorder": 2,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|LAMB2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_specified": 3,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 27,
    "not_specified|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 3,
    "not_specified|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Inborn_genetic_diseases": 18,
    "not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 14,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided": 15,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_specified|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Inborn_genetic_diseases|LAMB2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis|LAMB2-related_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder": 8,
    "not_provided|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 7,
    "Focal_segmental_glomerulosclerosis|Pierson_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Nephrotic_syndrome": 3,
    "Pierson_syndrome|Nephrotic_syndrome": 3,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|Nephrotic_syndrome": 5,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided|Kidney_disorder": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Glomerulonephritis": 1,
    "LAMB2-related_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 2,
    "not_provided|not_specified|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "LAMB2-related_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided": 3,
    "Focal_segmental_glomerulosclerosis|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 2,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "Kidney_disorder|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "Pierson_syndrome|Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome": 5,
    "not_specified|not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "Kidney_disorder|LAMB2-related_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "not_provided|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder": 1,
    "not_specified|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 2,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|focal_and_segmental_glomerulosclerosis|not_provided|Inborn_genetic_diseases": 1,
    "Pierson_syndrome|not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|LAMB2-related_disorder|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Kidney_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "LAMB2-related_disorder|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome": 2,
    "Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided": 4,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided": 8,
    "Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_specified": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided": 1,
    "LAMB2-related_disorder|Inborn_genetic_diseases|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Kidney_disorder": 1,
    "LAMB2-related_disorder|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 2,
    "not_specified|not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Kidney_disorder|Pierson_syndrome": 2,
    "not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_specified|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|LAMB2-related_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "Kidney_disorder|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 2,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 2,
    "Nephrotic_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "focal_and_segmental_glomerulosclerosis|Pierson_syndrome|Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder|Pierson_syndrome": 1,
    "not_provided|not_specified|Pierson_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided|LAMB2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_specified|Kidney_disorder": 1,
    "Inborn_genetic_diseases|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|Kidney_disorder|not_specified|not_provided": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Corticosteroids_response": 1,
    "Congenital_myasthenic_syndrome|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "not_specified|not_provided|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|LAMB2-related_disorder": 1,
    "LAMB2-related_disorder|Pierson_syndrome|not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome": 1,
    "not_specified|LAMB2-related_infantile-onset_nephrotic_syndrome|Kidney_disorder|Pierson_syndrome": 1,
    "Diffuse_mesangial_sclerosis|Inborn_genetic_diseases|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Corticosteroids_response": 31,
    "not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|LAMB2-related_disorder": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "LAMB2-related_disorder|Corticosteroids_response": 1,
    "not_provided|LAMB2-related_infantile-onset_nephrotic_syndrome|Kidney_disorder|Pierson_syndrome|not_specified": 1,
    "Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|not_specified|not_provided": 1,
    "not_specified|Pierson_syndrome|LAMB2-related_infantile-onset_nephrotic_syndrome|LAMB2-related_disorder|not_provided": 1,
    "LAMB2-related_infantile-onset_nephrotic_syndrome|Pierson_syndrome|LAMB2-related_disorder|not_provided": 1,
    "Nephrotic_syndrome|Pierson_syndrome": 4,
    "not_provided|Classic_Hodgkin_lymphoma": 1,
    "KLHDC8B-related_disorder": 1,
    "not_provided|KLHDC8B-related_disorder": 1,
    "Classic_Hodgkin_lymphoma|not_specified|not_provided": 1,
    "KLHDC8B-related_disorder|not_provided": 1,
    "GPX1_POLYMORPHISM|not_provided|Gluthathione_peroxidase_deficiency": 1,
    "Gluthathione_peroxidase_deficiency": 25,
    "GPX1-related_disorder": 3,
    "Gluthathione_peroxidase_deficiency|not_specified": 3,
    "not_specified|Gluthathione_peroxidase_deficiency": 1,
    "RHOA-related_disorder": 1,
    "Ectodermal_dysplasia_with_facial_dysmorphism_and_acral|_ocular|_and_brain_anomalies": 4,
    "not_provided|RHOA-related_disorder": 1,
    "neuro-ectodermal_phenotype|Ectodermal_dysplasia_with_facial_dysmorphism_and_acral|_ocular|_and_brain_anomalies|Hemihypertrophy|not_provided": 1,
    "not_provided|Glycine_encephalopathy": 92,
    "Glycine_encephalopathy": 2435,
    "Glycine_encephalopathy_1|Inborn_genetic_diseases|Glycine_encephalopathy": 4,
    "Glycine_encephalopathy_1|Glycine_encephalopathy": 52,
    "Inborn_genetic_diseases|Glycine_encephalopathy": 30,
    "Glycine_encephalopathy_1": 55,
    "Glycine_encephalopathy|Inborn_genetic_diseases": 42,
    "AMT-related_disorder|not_specified|Glycine_encephalopathy|not_provided": 1,
    "Glycine_encephalopathy|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Glycine_encephalopathy": 6,
    "not_provided|not_specified|Glycine_encephalopathy": 7,
    "Glycine_encephalopathy_1|Glycine_encephalopathy_2|Glycine_encephalopathy": 2,
    "not_specified|Glycine_encephalopathy_1|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy|not_provided": 95,
    "Glycine_encephalopathy_2": 11,
    "Glycine_encephalopathy|Glycine_encephalopathy_1": 40,
    "Glycine_encephalopathy_1|not_provided": 1,
    "not_provided|Glycine_encephalopathy|Glycine_encephalopathy_2": 2,
    "Glycine_encephalopathy|not_specified": 17,
    "Glycine_encephalopathy_1|Glycine_encephalopathy_2|Inborn_genetic_diseases|not_provided|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy|Glycine_encephalopathy_2|Glycine_encephalopathy_1": 2,
    "Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy": 15,
    "Glycine_encephalopathy_2|Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy|AMT-related_disorder|not_provided": 1,
    "Glycine_encephalopathy_2|Glycine_encephalopathy_1|Glycine_encephalopathy": 4,
    "not_specified|Glycine_encephalopathy": 7,
    "Glycine_encephalopathy_2|Glycine_encephalopathy": 2,
    "not_provided|Glycine_encephalopathy|Glycine_encephalopathy_1|Glycine_encephalopathy_2": 1,
    "Glycine_encephalopathy_1|Glycine_encephalopathy|not_specified": 2,
    "Glycine_encephalopathy|not_provided|AMT-related_disorder": 2,
    "Glycine_encephalopathy|Glycine_encephalopathy_2": 6,
    "Glycine_encephalopathy_1|Glycine_encephalopathy_2|Glycine_encephalopathy|not_provided": 1,
    "Glycine_encephalopathy_2|Glycine_encephalopathy|Glycine_encephalopathy_1": 1,
    "Inborn_genetic_diseases|Glycine_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Glycine_encephalopathy_2|not_specified|Glycine_encephalopathy": 1,
    "not_provided|Glycine_encephalopathy|not_specified": 3,
    "AMT-related_disorder|Glycine_encephalopathy|Glycine_encephalopathy_1|Inborn_genetic_diseases": 1,
    "Glycine_encephalopathy|AMT-related_disorder": 4,
    "Glycine_encephalopathy_1|Glycine_encephalopathy|not_specified|not_provided": 2,
    "AMT-related_disorder|Glycine_encephalopathy": 1,
    "not_specified|AMT-related_disorder|Glycine_encephalopathy_2|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy_2|Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy|Neurodevelopmental_delay": 1,
    "not_specified|not_provided|Glycine_encephalopathy": 11,
    "Glycine_encephalopathy_2|not_provided|Glycine_encephalopathy|Glycine_encephalopathy_1": 1,
    "Glycine_encephalopathy|AMT-related_disorder|Glycine_encephalopathy_2": 1,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|Glycine_encephalopathy_2": 1,
    "Glycine_encephalopathy_1|AMT-related_disorder|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy_2|Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy|See_cases": 1,
    "Glycine_encephalopathy_1|Glycine_encephalopathy|Glycine_encephalopathy_2": 1,
    "Glycine_encephalopathy_2|Glycine_encephalopathy_1|Inborn_genetic_diseases|Glycine_encephalopathy": 1,
    "not_specified|AMT-related_disorder|Glycine_encephalopathy": 1,
    "not_provided|Glycine_encephalopathy_1|Glycine_encephalopathy": 7,
    "Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy|Glycine_encephalopathy_2": 1,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|Neurodevelopmental_delay": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 147,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 188,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_provided": 31,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 5,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 5,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 18,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Inborn_genetic_diseases|not_provided": 5,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|DAG1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided": 26,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|DAG1-related_disorder|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_provided": 8,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 8,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_specified": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Inborn_genetic_diseases": 6,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified": 3,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 21,
    "DAG1-related_disorder|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|DAG1-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|DAG1-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Inborn_genetic_diseases": 9,
    "DAG1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|DAG1-related_disorder": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided": 4,
    "DAG1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 3,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Inborn_genetic_diseases": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided|not_specified": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|not_provided": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 14,
    "Elevated_circulating_creatine_kinase_concentration": 17,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Inborn_genetic_diseases": 1,
    "DAG1-related_disorder": 2,
    "Myopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided": 1,
    "DAG1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 2,
    "not_provided|DAG1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 1,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 2,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|DAG1-related_disorder": 1,
    "not_specified|DAG1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 4,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_alpha-dystroglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Inborn_genetic_diseases|not_provided": 1,
    "DAG1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|DAG1-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_provided|DAG1-related_disorder": 2,
    "DAG1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|DAG1-related_disorder|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2P|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A9|not_provided|Inborn_genetic_diseases": 1,
    "BSN-related_disorder": 43,
    "BSN_related_epilepsy": 2,
    "not_provided|BSN-related_disorder": 5,
    "BSN-associated_epilepsy": 1,
    "BSN-associated_seizure_disorder": 2,
    "not_specified|BSN-related_disorder": 2,
    "not_specified|BSN_related_epilepsy": 2,
    "Parkinsonian_disorder|Parkinson_disease|Vascular_parkinsonism": 1,
    "BSN-related_disorder|not_provided": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 163,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14": 29,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 10,
    "GMPPB-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "GMPPB-related_disorder": 7,
    "GMPPB-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_specified|not_provided": 1,
    "GMPPB-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_provided|Abnormality_of_the_musculature": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 16,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|GMPPB-related_disorder|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_provided": 16,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 5,
    "not_provided|GMPPB-related_disorder": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|GMPPB-related_disorder": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 5,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_provided": 1,
    "Inborn_genetic_diseases|GMPPB-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_provided|Abnormality_of_the_musculature": 1,
    "not_provided|Muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 6,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 1,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14": 2,
    "GMPPB-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|not_provided|Abnormality_of_the_musculature": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 4,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|not_provided": 1,
    "GMPPB-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_provided": 3,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Inborn_genetic_diseases|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_provided|Inborn_genetic_diseases": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_provided|not_specified": 3,
    "Abnormality_of_the_musculature|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|not_specified": 1,
    "Elevated_circulating_creatine_kinase_concentration|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Abnormality_of_the_musculature": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14": 1,
    "Myopathy_caused_by_variation_in_GMPPB": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "GMPPB-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T|Muscular_dystrophy|not_provided": 1,
    "GMPPB-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A14|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2T": 1,
    "UBA7-related_disorder": 10,
    "UBA7-related_disorder|not_specified": 1,
    "not_provided|Seckel_syndrome_9": 3,
    "Inborn_genetic_diseases|Seckel_syndrome_9": 1,
    "TRAIP-related_disorder|not_provided": 3,
    "not_provided|TRAIP-related_disorder": 4,
    "Seckel_syndrome_9": 4,
    "not_provided|Inborn_genetic_diseases|Seckel_syndrome_9": 1,
    "not_specified|Seckel_syndrome_9|not_provided": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_9|not_provided": 1,
    "not_specified|TRAIP-related_disorder|Seckel_syndrome_9|not_provided": 1,
    "not_specified|MST1R-related_disorder": 1,
    "MST1R-related_disorder": 14,
    "MST1R-related_disorder|not_provided": 1,
    "not_provided|MST1R-related_disorder": 2,
    "Nasopharyngeal_carcinoma|_susceptibility_to|_3|not_provided|MST1R-related_disorder": 1,
    "Nasopharyngeal_carcinoma|_susceptibility_to|_3": 2,
    "Congenital_diarrhea": 1,
    "SEMA3F-related_disorder": 195,
    "not_specified|SEMA3F-related_disorder|not_provided": 1,
    "SEMA3F-related_disorder|not_specified": 12,
    "not_specified|SEMA3F-related_disorder": 20,
    "not_provided|SEMA3F-related_disorder": 3,
    "SEMA3F-related_disorder|not_provided": 2,
    "SEMA3F-related_disorder|Hearing_impairment": 1,
    "Hypogonadotropic_hypogonadism|not_specified": 1,
    "not_provided|Congenital_Stationary_Night_Blindness|_Dominant": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_3": 32,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_3": 6,
    "Congenital_stationary_night_blindness_autosomal_dominant_3|not_provided": 7,
    "not_provided|GNAT1-related_disorder": 2,
    "GNAT1-related_disorder|not_provided": 1,
    "Congenital_stationary_night_blindness_1C": 57,
    "Congenital_stationary_night_blindness_autosomal_dominant_3|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_stationary_night_blindness_1G": 3,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_3|Congenital_stationary_night_blindness_1G": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_3|GNAT1-related_disorder|not_specified|not_provided": 2,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_3|GNAT1-related_disorder": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_3|Congenital_stationary_night_blindness_1G": 2,
    "Congenital_stationary_night_blindness_1G|Congenital_stationary_night_blindness_autosomal_dominant_3|not_provided": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_3|GNAT1-related_disorder": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_3|GNAT1-related_disorder|not_provided": 2,
    "not_provided|Congenital_stationary_night_blindness_1G": 1,
    "Developmental_and_epileptic_encephalopathy_102": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy_102": 1,
    "GNAI2-related_disorder": 2,
    "Familial_ventricular_tachycardia": 1,
    "Pituitary_dependent_hypercortisolism": 5,
    "not_provided|Ovarian_granulosa_cell_tumor|Thecoma|_somatic|Adrenocortical_tumor|_somatic": 2,
    "Motor_delay|Hypopituitarism|Retractile_testis|Short_stature|Recurrent_infections|Decreased_circulating_total_IgM": 1,
    "Ventricular_tachycardia|_somatic": 1,
    "SEMA3B-related_disorder|not_specified": 3,
    "SEMA3B-related_disorder": 175,
    "not_specified|SEMA3B-related_disorder": 5,
    "Auroneurodental_syndrome|See_cases": 1,
    "Deficiency_of_hyaluronoglucosaminidase|not_provided": 5,
    "Deficiency_of_hyaluronoglucosaminidase": 343,
    "not_provided|Deficiency_of_hyaluronoglucosaminidase": 4,
    "not_specified|Deficiency_of_hyaluronoglucosaminidase": 10,
    "Deficiency_of_hyaluronoglucosaminidase|not_specified": 12,
    "not_specified|not_provided|Deficiency_of_hyaluronoglucosaminidase": 2,
    "HYAL1-related_disorder|Deficiency_of_hyaluronoglucosaminidase|not_provided": 1,
    "Deficiency_of_hyaluronoglucosaminidase|HYAL1-related_disorder": 2,
    "HYAL1-related_disorder|Deficiency_of_hyaluronoglucosaminidase": 2,
    "HYAL1-related_disorder": 1,
    "Deficiency_of_hyaluronoglucosaminidase|HYAL1-related_disorder|not_specified|not_provided": 1,
    "HYAL1-related_disorder|not_provided|Deficiency_of_hyaluronoglucosaminidase": 1,
    "not_provided|HYAL1-related_disorder|Deficiency_of_hyaluronoglucosaminidase": 1,
    "HYAL2_deficiency": 3,
    "HYAL2_deficiency|Muggenthaler-Chowdhury-Chioza_syndrome": 8,
    "HYAL2-related_disorder": 8,
    "Cleft_lip_and_palate-craniofacial_dysmorphism-congenital_heart_defect-hearing_loss_syndrome": 1,
    "HYAL2_deficiency|Muggenthaler-Chowdhury-Chioza_syndrome|HYAL2-related_disorder": 1,
    "not_provided|HYAL2-related_disorder": 1,
    "HYAL2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_22": 6,
    "Primary_ciliary_dyskinesia_22": 11,
    "Primary_ciliary_dyskinesia|ZMYND10-related_disorder": 4,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_22": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_22": 2,
    "not_provided|ZMYND10-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_22|Primary_ciliary_dyskinesia": 4,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|ZMYND10-related_disorder|not_provided": 1,
    "ZMYND10-related_disorder|Primary_ciliary_dyskinesia_22": 1,
    "ZMYND10-related_disorder": 1,
    "Primary_ciliary_dyskinesia_22|Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_22": 1,
    "ZMYND10-related_disorder|Primary_ciliary_dyskinesia_22|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_22|ZMYND10-related_disorder": 1,
    "ZMYND10-related_disorder|Primary_ciliary_dyskinesia_22|not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_2": 33,
    "Epilepsy|_familial_focal|_with_variable_foci_2|NPRL2-related_disorder|not_provided": 1,
    "Familial_focal_epilepsy_with_variable_foci": 1378,
    "Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_2": 3,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_2": 2,
    "NPRL2-related_disorder": 4,
    "NPRL2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|NPRL2-related_disorder": 1,
    "Inborn_genetic_diseases|NPRL2-related_disorder": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_2|Seizure|Inborn_genetic_diseases|not_provided": 1,
    "Neonatal_respiratory_distress": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_2|not_provided|Inborn_genetic_diseases": 1,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|CACNA2D2-related_disorder|not_provided": 1,
    "CACNA2D2-related_disorder|Developmental_and_epileptic_encephalopathy": 8,
    "Developmental_and_epileptic_encephalopathy|CACNA2D2-related_disorder": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay": 2,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Developmental_and_epileptic_encephalopathy": 7,
    "Inborn_genetic_diseases|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Developmental_and_epileptic_encephalopathy": 1,
    "CACNA2D2-related_disorder": 3,
    "Inborn_genetic_diseases|CACNA2D2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Inborn_genetic_diseases": 1,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay": 1,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|CACNA2D2-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Inborn_genetic_diseases": 1,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay": 2,
    "Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy|not_specified|Inborn_genetic_diseases": 1,
    "CACNA2D2-related_disorder|Cerebellar_atrophy_with_seizures_and_variable_developmental_delay|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "CISH-related_disorder": 2,
    "not_provided|CISH-related_disorder": 1,
    "Bacteremia|_susceptibility_to|_2|Tuberculosis|_susceptibility_to|Malaria|_susceptibility_to": 1,
    "not_provided|Patterned_macular_dystrophy_3": 1,
    "not_provided|MAPKAPK3-related_disorder": 2,
    "Patterned_macular_dystrophy_3": 2,
    "MAPKAPK3-related_disorder|not_provided": 1,
    "DOCK3-related_disorder": 16,
    "Inborn_genetic_diseases|DOCK3-related_disorder": 1,
    "DOCK3-related_disorder|not_provided": 7,
    "Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia|Inborn_genetic_diseases": 3,
    "Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia": 8,
    "not_provided|DOCK3-related_disorder": 6,
    "Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia|Global_developmental_delay|Hypotonia": 2,
    "not_specified|Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia|DOCK3-related_disorder": 1,
    "Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_impaired_intellectual_development|_hypotonia|_and_ataxia": 1,
    "not_specified|DOCK3-related_disorder": 1,
    "MANF-related_disorder": 4,
    "Diabetes|_deafness|_developmental_delay|_and_short_stature_syndrome": 2,
    "Diabetes|_deafness|_developmental_delay|_and_short_stature_syndrome|Cerebro-costo-mandibular_syndrome": 1,
    "Cerebro-costo-mandibular_syndrome": 6,
    "TOP2_deficiency_type_1": 1,
    "Inborn_genetic_diseases|Aminoacylase_1_deficiency": 2,
    "Aminoacylase_1_deficiency": 17,
    "not_provided|ACY1-related_disorder": 3,
    "ACY1-related_disorder|not_provided": 3,
    "not_provided|ABHD14A-ACY1-related_disorder": 1,
    "ABHD14A-ACY1-related_disorder|not_provided": 1,
    "Aminoacylase_1_deficiency|not_provided": 3,
    "ACY1-related_disorder": 3,
    "not_provided|ACY1-related_disorder|Aminoacylase_1_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Aminoacylase_1_deficiency": 1,
    "Aminoacylase_1_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Aminoacylase_1_deficiency|Inborn_genetic_diseases": 1,
    "Aminoacylase_1_deficiency|Inborn_aminoacylase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Aminoacylase_1_deficiency": 1,
    "not_specified|not_provided|Aminoacylase_1_deficiency": 1,
    "Aminoacylase_1_deficiency|not_provided|ACY1-related_disorder": 2,
    "ACY1-related_disorder|not_specified|not_provided|Aminoacylase_1_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome": 1,
    "POC1A-related_syndrome": 2,
    "Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome": 18,
    "Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome|See_cases|POC1A-related_disorder": 1,
    "not_provided|POC1A-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome": 1,
    "Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome|not_provided": 1,
    "not_provided|Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome": 3,
    "POC1A-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome|not_provided": 2,
    "Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome|Inborn_genetic_diseases": 1,
    "Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome|not_specified|not_provided": 1,
    "Short_stature-onychodysplasia-facial_dysmorphism-hypotrichosis_syndrome|not_provided|Ateleiotic_dwarfism": 1,
    "not_provided|D-Glyceric_aciduria": 5,
    "D-Glyceric_aciduria": 8,
    "not_provided|GLYCTK-related_disorder": 3,
    "D-Glyceric_aciduria|GLYCTK-related_disorder|not_provided": 1,
    "D-Glyceric_aciduria|not_provided": 2,
    "GLYCTK-related_disorder": 3,
    "GLYCTK-related_disorder|not_provided": 3,
    "not_specified|GLYCTK-related_disorder": 1,
    "not_specified|D-Glyceric_aciduria": 2,
    "not_provided|not_specified|D-Glyceric_aciduria": 1,
    "GLYCTK-related_disorder|not_specified": 1,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 1567,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided|DNAH1-related_disorder": 12,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 120,
    "not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 53,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|Primary_ciliary_dyskinesia": 7,
    "not_provided|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 64,
    "Ciliary_dyskinesia|_primary|_37": 15,
    "DNAH1-related_disorder|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 39,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified": 63,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|DNAH1-related_disorder": 16,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided": 69,
    "not_specified|not_provided|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 4,
    "not_specified|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 16,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|DNAH1-related_disorder|not_specified": 1,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|not_specified": 8,
    "not_provided|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 4,
    "not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided|DNAH1-related_disorder": 1,
    "not_provided|DNAH1-related_disorder|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 10,
    "not_provided|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|DNAH1-related_disorder": 3,
    "Primary_ciliary_dyskinesia|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 2,
    "not_provided|not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 3,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|DNAH1-related_disorder": 4,
    "DNAH1-related_disorder|not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided": 1,
    "DNAH1-related_disorder": 15,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|not_provided": 8,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|Premature_ovarian_insufficiency|not_provided": 1,
    "DNAH1-related_disorder|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided": 3,
    "Non-syndromic_male_infertility_due_to_sperm_motility_disorder": 3,
    "not_provided|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified": 10,
    "DNAH1-related_disorder|not_specified|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|Kartagener_syndrome": 1,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified|not_provided": 3,
    "not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|DNAH1-related_disorder": 4,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|Adams-Oliver_syndrome_6": 1,
    "not_specified|Primary_ciliary_dyskinesia": 248,
    "Primary_ciliary_dyskinesia_2": 11,
    "DNAH1-related_disorder|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 2,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|DNAH1-related_disorder|not_provided": 5,
    "DNAH1-related_disorder|not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 1,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided|Primary_ciliary_dyskinesia": 2,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified|DNAH1-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|Primary_ciliary_dyskinesia|DNAH1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 1,
    "DNAH1-related_disorder|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified": 2,
    "not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided": 2,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified|Primary_ciliary_dyskinesia": 1,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_specified|not_provided|DNAH1-related_disorder": 1,
    "not_provided|not_specified|DNAH1-related_disorder": 1,
    "not_specified|not_provided|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 1,
    "not_provided|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|Primary_ciliary_dyskinesia": 1,
    "DNAH1-related_disorder|not_provided": 1,
    "Spermatogenic_failure_18|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18|DNAH1-related_disorder|not_provided": 1,
    "not_provided|DNAH1-related_disorder|not_specified|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 1,
    "not_specified|DNAH1-related_disorder": 1,
    "Oligosynaptic_infertility|Ciliary_dyskinesia|_primary|_37|Primary_ciliary_dyskinesia|Spermatogenic_failure_18": 1,
    "Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided|not_specified": 1,
    "DNAH1-related_disorder|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|Spermatogenic_failure_18|Ciliary_dyskinesia|_primary|_37": 1,
    "Primary_ciliary_dyskinesia|not_specified|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 1,
    "Ciliary_dyskinesia|_primary|_37|not_provided|Spermatogenic_failure_18": 1,
    "Intellectual_disability|not_specified|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 1,
    "Intellectual_disability|Ciliary_dyskinesia|_primary|_37|Spermatogenic_failure_18": 1,
    "BAP1-related_tumor_predisposition_syndrome": 999,
    "not_provided|BAP1-related_tumor_predisposition_syndrome": 10,
    "BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder": 1,
    "BAP1-related_disorder": 4,
    "BAP1-related_tumor_predisposition_syndrome|not_provided": 13,
    "not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 535,
    "BAP1-related_tumor_predisposition_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 421,
    "BAP1-related_tumor_predisposition_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome": 47,
    "BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome|not_specified": 2,
    "Neurodevelopmental_disorder|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided": 40,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 28,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 41,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "BAP1-related_tumor_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 24,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BAP1-related_tumor_predisposition_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome": 5,
    "Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_specified": 10,
    "Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome": 3,
    "BAP1-related_disorder|not_provided|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 4,
    "BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|BAP1-related_tumor_predisposition_syndrome|not_provided": 1,
    "not_provided|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 37,
    "BAP1-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|BAP1-related_disorder|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided": 2,
    "Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "BAP1-related_disorder|Ganglioglioma|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BAP1-related_tumor_predisposition_syndrome|not_provided": 2,
    "not_provided|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_disorder|not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BAP1-related_tumor_predisposition_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided": 1,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_disorder": 2,
    "BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "BAP1-related_tumor_predisposition_syndrome|not_specified": 6,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_tumor_predisposition_syndrome": 3,
    "Melanoma|_uveal|_susceptibility_to|_2|BAP1_Cancer_Syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|BAP1-related_tumor_predisposition_syndrome": 5,
    "not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 5,
    "not_provided|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided": 1,
    "Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_specified|Melanoma|_uveal|_susceptibility_to|_2|not_provided": 1,
    "BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_provided|BAP1-related_disorder": 1,
    "BAP1-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome": 1,
    "Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|not_specified": 1,
    "BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 2,
    "BAP1-related_tumor_predisposition_syndrome|not_provided|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_disorder": 1,
    "BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome": 1,
    "Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome|not_specified|Hereditary_cancer": 1,
    "BAP1-related_tumor_predisposition_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Medulloblastoma": 1,
    "BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided|Melanoma|_uveal|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome": 1,
    "Uveal_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2": 1,
    "Uveal_melanoma|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome": 2,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Kury-Isidor_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome": 1,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_disorder": 1,
    "BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|not_provided|BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Kury-Isidor_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_tumor_predisposition_syndrome|not_specified": 1,
    "not_provided|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|BAP1-related_tumor_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|not_specified|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome|BAP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_tumor_predisposition_syndrome": 1,
    "Clear_cell_carcinoma_of_kidney|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "BAP1-related_disorder|not_specified|BAP1-related_tumor_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Kury-Isidor_syndrome|Neurodevelopmental_disorder|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Kury-Isidor_syndrome|Melanoma|_uveal|_susceptibility_to|_2": 1,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|BAP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Astrocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BAP1-related_tumor_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome|not_provided|See_cases": 1,
    "BAP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_specified|not_provided|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Kury-Isidor_syndrome": 1,
    "Melanoma|_uveal|_susceptibility_to|_2|BAP1-related_tumor_predisposition_syndrome|Kury-Isidor_syndrome": 1,
    "Neurodevelopmental_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "BAP1-related_tumor_predisposition_syndrome|See_cases|Kury-Isidor_syndrome|Neurodevelopmental_disorder|BAP1-associated_neurodevelopmental_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ewing_sarcoma|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_disorder|BAP1-related_tumor_predisposition_syndrome|not_provided": 2,
    "BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2": 1,
    "Kury-Isidor_syndrome|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_specified|BAP1-related_tumor_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_disorder": 1,
    "Neurodevelopmental_disorder|not_provided|BAP1-related_tumor_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome|Melanoma|_uveal|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma|_uveal|_susceptibility_to|_2|Kury-Isidor_syndrome|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_provided|not_specified|BAP1-related_tumor_predisposition_syndrome": 1,
    "Kury-Isidor_syndrome|Neurodevelopmental_disorder|not_provided": 1,
    "Kury-Isidor_syndrome|Neurodevelopmental_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|BAP1-related_disorder|not_specified|BAP1-related_tumor_predisposition_syndrome": 1,
    "not_provided|PHF7-related_disorder": 1,
    "PHF7-related_disorder": 1,
    "SEMA3G-related_disorder": 232,
    "not_specified|SEMA3G-related_disorder": 25,
    "SEMA3G-related_disorder|not_specified": 26,
    "SEMA3G-related_disorder|not_provided": 2,
    "Dilated_cardiomyopathy_1Z|not_provided|Hypertrophic_cardiomyopathy_13": 2,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 88,
    "not_provided|TNNC1-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 74,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_specified": 3,
    "not_provided|Dilated_cardiomyopathy_1Z": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 17,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 1,
    "Dilated_cardiomyopathy_1Z": 5,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_specified|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 2,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 2,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified": 4,
    "not_specified|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 3,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|Cardiovascular_phenotype": 10,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified": 2,
    "not_specified|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 5,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "not_provided|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 5,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype|TNNC1-related_disorder|not_provided": 1,
    "TNNC1-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype": 4,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided": 1,
    "TNNC1-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided": 2,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 2,
    "not_specified|TNNC1-related_disorder|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_provided": 4,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_provided": 3,
    "not_provided|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|TNNC1-related_disorder|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 3,
    "not_specified|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype": 1,
    "TNNC1-related_disorder|not_specified|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 4,
    "TNNC1-related_disorder|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Cardiomyopathy|TNNC1-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype|Dilated_cardiomyopathy_1S|not_provided": 1,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_specified": 1,
    "Dilated_cardiomyopathy_1Z|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Z": 1,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiomyopathy": 1,
    "TNNC1-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_13": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1Z|Hypertrophic_cardiomyopathy_13|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_13|Dilated_cardiomyopathy_1Z|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Isolated_hyperferritinemia": 4,
    "not_specified|Isolated_hyperferritinemia": 1,
    "Clear_cell_carcinoma_of_kidney": 1,
    "PBRM1-related_BAFopathy": 1,
    "not_provided|GLT8D1-related_disorder": 1,
    "Ciliopathy": 18,
    "ITIH4-related_disorder": 18,
    "not_provided|ITIH4-related_disorder": 1,
    "Hypercholesterolemia|_susceptibility_to": 1,
    "ITIH4-related_disorder|not_provided": 1,
    "Preeclampsia|Normal_pregnancy|Large_for_gestational_age": 2,
    "RFT1-congenital_disorder_of_glycosylation": 399,
    "RFT1-congenital_disorder_of_glycosylation|not_provided": 22,
    "not_provided|RFT1-congenital_disorder_of_glycosylation": 9,
    "RFT1-congenital_disorder_of_glycosylation|RFT1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|RFT1-congenital_disorder_of_glycosylation": 14,
    "RFT1-congenital_disorder_of_glycosylation|not_specified": 2,
    "RFT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|RFT1-congenital_disorder_of_glycosylation|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|RFT1-congenital_disorder_of_glycosylation": 1,
    "RFT1-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|RFT1-related_disorder|RFT1-congenital_disorder_of_glycosylation|not_provided": 1,
    "RFT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_specified": 1,
    "RFT1_related_CDG|RFT1-congenital_disorder_of_glycosylation": 1,
    "not_specified|RFT1-congenital_disorder_of_glycosylation": 6,
    "not_provided|RFT1-congenital_disorder_of_glycosylation|RFT1-related_disorder": 1,
    "RFT1-congenital_disorder_of_glycosylation|RFT1-related_disorder": 2,
    "RFT1-related_disorder|RFT1-congenital_disorder_of_glycosylation": 5,
    "RFT1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "not_provided|not_specified|RFT1-congenital_disorder_of_glycosylation": 2,
    "RFT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|RFT1-related_disorder": 1,
    "not_provided|RFT1-congenital_disorder_of_glycosylation|not_specified": 1,
    "not_specified|not_provided|RFT1-congenital_disorder_of_glycosylation": 1,
    "not_provided|Inborn_genetic_diseases|RFT1-congenital_disorder_of_glycosylation": 1,
    "RFT1-related_disorder|not_provided|RFT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 433,
    "Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|not_provided": 19,
    "not_provided|Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 2,
    "not_specified|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|not_provided": 3,
    "Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|Inborn_genetic_diseases": 11,
    "not_provided|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 6,
    "not_provided|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|not_specified": 1,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 13,
    "PRKCD-related_disorder|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 2,
    "PRKCD-related_disorder": 2,
    "Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|PRKCD-related_disorder": 3,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|PRKCD-related_disorder|not_provided": 2,
    "not_provided|PRKCD-related_disorder|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 1,
    "not_specified|not_provided|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 2,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|not_specified": 1,
    "Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Autoimmune_lymphoproliferative_syndrome|_type_III_caused_by_mutation_in_PRKCD": 1,
    "Transketolase_deficiency": 8,
    "Transketolase_deficiency|not_provided": 3,
    "not_provided|TKT-related_disorder": 3,
    "not_provided|Transketolase_deficiency": 4,
    "TKT-related_disorder": 6,
    "not_provided|TKT-related_disorder|Transketolase_deficiency": 1,
    "not_specified|Transketolase_deficiency": 1,
    "Sinoatrial_node_dysfunction_and_deafness|not_provided|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 3,
    "Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_provided": 3,
    "not_specified|CACNA1D-related_disorder|not_provided|Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 1,
    "Autosomal_recessive_Alport_syndrome|Sinoatrial_node_dysfunction_and_deafness": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness|not_provided|not_specified": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 23,
    "CACNA1D-related_disorder|not_provided": 18,
    "Sinoatrial_node_dysfunction_and_deafness": 12,
    "CACNA1D-related_disorder": 13,
    "CACNA1D-related_neurodevelopmental_and_endocrine_disorders|not_provided": 1,
    "not_provided|VATER_association": 3,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_specified|not_provided": 2,
    "Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_specified|not_provided|CACNA1D-related_disorder": 2,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_provided": 4,
    "not_provided|CACNA1D-related_disorder": 16,
    "Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Sinoatrial_node_dysfunction_and_deafness|Meniere_disease": 1,
    "Sinoatrial_node_dysfunction_and_deafness|not_provided": 3,
    "not_provided|Sinoatrial_node_dysfunction_and_deafness": 2,
    "not_provided|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_specified": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness|Congenital_anomaly_of_kidney_and_urinary_tract|Inborn_genetic_diseases|not_provided": 1,
    "CACNA1D-related_disorder|not_specified|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness": 1,
    "not_provided|Sinoatrial_node_dysfunction_and_deafness|Inborn_genetic_diseases": 2,
    "not_provided|CACNA1D-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 2,
    "not_specified|Sinoatrial_node_dysfunction_and_deafness|not_provided": 1,
    "not_provided|Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 5,
    "not_provided|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 3,
    "Congenital_disorder_of_glycosylation|_type_Iw|_autosomal_dominant": 12,
    "not_provided|Sinoatrial_node_dysfunction_and_deafness|not_specified": 1,
    "not_provided|not_specified|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 2,
    "not_provided|Sinoatrial_node_dysfunction_and_deafness|not_specified|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness|not_provided": 4,
    "not_specified|CACNA1D-related_disorder|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_specified|not_provided|CACNA1D-related_disorder": 1,
    "CACNA1D-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CACNA1D-related_disorder": 2,
    "Inborn_genetic_diseases|Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CACNA1D-related_disorder|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_specified": 1,
    "not_specified|CACNA1D-related_disorder": 1,
    "not_provided|Congenital_anomaly_of_kidney_and_urinary_tract|not_specified|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|CACNA1D-related_disorder": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness": 2,
    "Inborn_genetic_diseases|not_provided|CACNA1D-related_disorder": 1,
    "not_specified|not_provided|CACNA1D-related_disorder|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 2,
    "CACNA1D-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|CACNA1D-related_disorder|not_provided": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|Sinoatrial_node_dysfunction_and_deafness|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Sinoatrial_node_dysfunction_and_deafness": 1,
    "not_specified|not_provided|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 2,
    "not_specified|not_provided|Dystonia|_early-onset|_and/or_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_provided|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities": 1,
    "Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_provided|not_specified": 1,
    "not_specified|Sinoatrial_node_dysfunction_and_deafness|Aldosterone-producing_adenoma_with_seizures_and_neurological_abnormalities|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|CACNA1D-related_disorder": 1,
    "Inborn_genetic_diseases|CACNA1D-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|CACNA1D-related_disorder": 1,
    "CACNA2D3-related_disorder": 26,
    "CACNA2D3-related_disorder|not_provided": 1,
    "CACNA2D3-related_disorder|not_specified": 1,
    "not_specified|CACNA2D3-related_disorder": 1,
    "Autosomal_dominant_Robinow_syndrome_1|not_provided": 19,
    "not_provided|WNT5A-related_disorder": 5,
    "not_provided|Autosomal_dominant_Robinow_syndrome_1": 13,
    "WNT5A-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Robinow_syndrome": 1,
    "WNT5A-related_disorder": 6,
    "not_provided|WNT5A-related_disorder|Autosomal_dominant_Robinow_syndrome_1": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_Robinow_syndrome_1|not_provided": 2,
    "Autosomal_dominant_Robinow_syndrome_1|WNT5A-related_disorder": 1,
    "WNT5A-related_disorder|not_specified|not_provided": 1,
    "Leukoencephalopathy|_motor_delay|_spasticity|_and_dysarthria_syndrome": 6,
    "Autosomal_dominant_Robinow_syndrome_1|Inborn_genetic_diseases": 1,
    "WNT5A-related_disorder|not_provided": 2,
    "WNT5A-related_disorder|not_provided|Autosomal_dominant_Robinow_syndrome_1": 1,
    "not_specified|not_provided|Autosomal_dominant_Robinow_syndrome_1": 1,
    "IL17RD-related_disorder|HYPOGONADOTROPIC_HYPOGONADISM_18_WITH_ANOSMIA|_SUSCEPTIBILITY_TO": 1,
    "Hypogonadotropic_hypogonadism_18_with_or_without_anosmia": 6,
    "IL17RD-related_disorder": 9,
    "IL17RD-related_disorder|not_provided": 4,
    "Hypogonadotropic_hypogonadism_18_with_anosmia": 2,
    "not_specified|Hypogonadotropic_hypogonadism_18_with_or_without_anosmia": 1,
    "not_provided|not_specified|IL17RD-related_disorder": 1,
    "not_provided|IL17RD-related_disorder": 4,
    "not_provided|Hypogonadotropic_hypogonadism_18_with_or_without_anosmia": 2,
    "Hypogonadotropic_hypogonadism_18_with_or_without_anosmia|not_provided|not_specified": 2,
    "Hypogonadism": 1,
    "HYPOGONADOTROPIC_HYPOGONADISM_18_WITH_ANOSMIA|_SUSCEPTIBILITY_TO": 1,
    "IL17RD-related_disorder|not_provided|not_specified": 1,
    "Hypogonadotropic_hypogonadism_18_with_or_without_anosmia|not_provided": 2,
    "not_specified|Hypogonadotropic_hypogonadism_18_with_or_without_anosmia|not_provided": 1,
    "Delayed_puberty": 3,
    "not_specified|not_provided|Cerebral_arteriovenous_malformation|Delayed_puberty": 1,
    "not_specified|Hypogonadotropic_hypogonadism_18_with_anosmia|Delayed_puberty|not_provided": 1,
    "not_specified|IL17RD-related_disorder": 1,
    "Septo-optic_dysplasia_sequence|Combined_Pituitary_Hormone_Deficiency|_Dominant/Recessive": 1,
    "HESX1-related_disorder": 2,
    "Inborn_genetic_diseases|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|not_provided": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|not_specified|not_provided": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES": 24,
    "HESX1-related_disorder|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|SEPTOOPTIC_DYSPLASIA|_MILD|not_provided": 1,
    "GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|not_provided|Inborn_genetic_diseases": 1,
    "GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence": 22,
    "not_provided|Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|HESX1-related_disorder|HESX1-Related_Disorders": 1,
    "GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|Inborn_genetic_diseases": 4,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|not_specified": 1,
    "PITUITARY_HORMONE_DEFICIENCY|_COMBINED|_5": 3,
    "GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Inborn_genetic_diseases|HESX1-related_disorder|not_provided|Pituitary_hormone_deficiency|_combined|_1|Amenorrhea": 1,
    "Septo-optic_dysplasia_sequence|not_provided|not_specified|Combined_Pituitary_Hormone_Deficiency|_Dominant/Recessive|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES": 1,
    "not_provided|Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|Inborn_genetic_diseases|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence": 1,
    "not_provided|Septo-optic_dysplasia_sequence": 2,
    "Septo-optic_dysplasia_sequence|Male_infertility_with_spermatogenesis_disorder|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|not_provided": 1,
    "Pituitary_hormone_deficiency|_combined|_1|Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|not_specified": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Pituitary_hormone_deficiency|_combined|_1|Septo-optic_dysplasia_sequence": 1,
    "Pituitary_hormone_deficiency|_combined|_1|Septo-optic_dysplasia_sequence": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Combined_Pituitary_Hormone_Deficiency|_Dominant/Recessive|Inborn_genetic_diseases": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Inborn_genetic_diseases": 1,
    "Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|not_provided": 1,
    "Pituitary_hormone_deficiency|_combined|_1|Septo-optic_dysplasia_sequence|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|not_provided": 1,
    "not_provided|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|Inborn_genetic_diseases": 1,
    "Septo-optic_dysplasia_sequence|Inborn_genetic_diseases|HESX1-related_disorder|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES": 1,
    "not_specified|GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|not_provided": 2,
    "GROWTH_HORMONE_DEFICIENCY_WITH_PITUITARY_ANOMALIES|Septo-optic_dysplasia_sequence|PITUITARY_HORMONE_DEFICIENCY|_COMBINED|_5|not_specified|not_provided": 1,
    "Septo-optic_dysplasia_sequence|not_specified": 1,
    "HESX1-related_disorder|not_specified": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Dominant/Recessive|Septo-optic_dysplasia_sequence": 4,
    "not_specified|APPL1-related_disorder|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_14|not_provided|not_specified": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_14": 3,
    "Maturity-onset_diabetes_of_the_young_type_14": 4,
    "APPL1-related_disorder|Maturity-onset_diabetes_of_the_young_type_14|not_provided|not_specified": 2,
    "Maturity-onset_diabetes_of_the_young_type_14|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_14|APPL1-related_disorder|not_provided|not_specified": 1,
    "APPL1-related_disorder|not_provided": 1,
    "APPL1-related_disorder": 6,
    "Maturity-onset_diabetes_of_the_young_type_14|not_provided": 2,
    "not_specified|not_provided|APPL1-related_disorder": 1,
    "not_specified|Monogenic_diabetes": 9,
    "not_provided|APPL1-related_disorder": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_14": 1,
    "APPL1-related_disorder|Monogenic_diabetes|not_provided": 1,
    "ASB14-related_condition": 1,
    "SPERMATOGENIC_FAILURE_100": 2,
    "Long_QT_syndrome|Brugada_syndrome": 2,
    "SLMAP-related_disorder": 3,
    "SLMAP-related_disorder|not_specified|Brugada_syndrome": 1,
    "Brugada_syndrome|not_specified|SLMAP-related_disorder": 1,
    "not_provided|not_specified|Brugada_syndrome": 6,
    "FLNB-Related_Spectrum_Disorders": 67,
    "FLNB-Related_Spectrum_Disorders|not_provided": 42,
    "not_specified|FLNB-Related_Spectrum_Disorders|not_provided": 4,
    "not_specified|FLNB-related_disorder|not_provided|FLNB-Related_Spectrum_Disorders": 2,
    "Spondylocarpotarsal_synostosis_syndrome": 31,
    "not_specified|not_provided|Connective_tissue_disorder|FLNB-related_disorder": 1,
    "Larsen_syndrome|Boomerang_dysplasia": 1,
    "FLNB-related_disorder|not_provided": 22,
    "FLNB-Related_Spectrum_Disorders|not_specified|not_provided": 14,
    "not_provided|FLNB-related_disorder": 17,
    "FLNB-related_disorder|Connective_tissue_disorder|not_specified|not_provided": 1,
    "Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Connective_tissue_disorder|not_provided|FLNB-Related_Spectrum_Disorders|not_specified": 1,
    "not_specified|not_provided|FLNB-Related_Spectrum_Disorders": 5,
    "not_provided|FLNB-Related_Spectrum_Disorders|not_specified": 5,
    "Short_stature|Abnormality_of_the_vertebral_column|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|Connective_tissue_disorder|not_specified": 1,
    "Atelosteogenesis_type_I": 14,
    "Connective_tissue_disorder|Larsen_syndrome": 1,
    "Larsen_syndrome": 34,
    "Larsen_syndrome|not_provided": 3,
    "FLNB-related_disorder|Inborn_genetic_diseases|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|not_provided|See_cases": 1,
    "Boomerang_dysplasia": 2,
    "Atelosteogenesis_type_I|not_provided": 1,
    "FLNB-related_disorder": 24,
    "not_provided|Atelosteogenesis_type_III": 2,
    "Atelosteogenesis_type_III": 7,
    "Atelosteogenesis_type_I|Atelosteogenesis_type_III": 1,
    "FLNB-related_disorder|not_provided|Larsen_syndrome": 1,
    "not_provided|not_specified|FLNB-Related_Spectrum_Disorders": 4,
    "FLNB-Related_Spectrum_Disorders|Inborn_genetic_diseases|Atelosteogenesis_type_I|Atelosteogenesis_type_III|not_provided": 1,
    "Connective_tissue_disorder|FLNB-Related_Spectrum_Disorders|not_specified|not_provided": 5,
    "not_provided|FLNB-Related_Spectrum_Disorders": 18,
    "Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Connective_tissue_disorder|not_specified|Inborn_genetic_diseases|FLNB-Related_Spectrum_Disorders|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|FLNB-related_disorder": 7,
    "Connective_tissue_disorder|FLNB-Related_Spectrum_Disorders|not_provided|FLNB-related_disorder": 1,
    "not_provided|Spondylocarpotarsal_synostosis_syndrome": 5,
    "Inborn_genetic_diseases|Atelosteogenesis_type_I": 1,
    "not_provided|Larsen_syndrome": 3,
    "Connective_tissue_disorder|FLNB-related_disorder|not_provided": 1,
    "Spondylocarpotarsal_synostosis_syndrome|not_provided": 3,
    "Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_III|Larsen_syndrome": 6,
    "Inborn_genetic_diseases|FLNB-Related_Spectrum_Disorders": 1,
    "not_specified|FLNB-Related_Spectrum_Disorders|not_provided|Connective_tissue_disorder|FLNB-related_disorder|Inborn_genetic_diseases": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|Connective_tissue_disorder": 3,
    "Larsen_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|FLNB-related_disorder|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|FLNB-Related_Spectrum_Disorders|not_provided": 6,
    "FLNB-Related_Spectrum_Disorders|FLNB-related_disorder|not_provided": 2,
    "FLNB-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "FLNB-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|FLNB-related_disorder|not_specified|not_provided": 2,
    "Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "FLNB-Related_Spectrum_Disorders|not_specified|Connective_tissue_disorder|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_provided|FLNB-related_disorder": 2,
    "Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Larsen_syndrome|Spondylocarpotarsal_synostosis_syndrome": 1,
    "not_provided|Spondylocarpotarsal_synostosis_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Boomerang_dysplasia": 1,
    "Connective_tissue_disorder|FLNB-Related_Spectrum_Disorders|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|FLNB-related_disorder": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Atelosteogenesis_type_III|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_I|Boomerang_dysplasia|Larsen_syndrome|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|not_specified|not_provided|Connective_tissue_disorder": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|Spondylocarpotarsal_synostosis_syndrome": 2,
    "FLNB-related_disorder|FLNB-Related_Spectrum_Disorders|not_provided": 3,
    "not_specified|not_provided|Inborn_genetic_diseases|Connective_tissue_disorder": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|Inborn_genetic_diseases": 5,
    "not_provided|not_specified|Boomerang_dysplasia|Atelosteogenesis_type_III|Larsen_syndrome|Atelosteogenesis_type_I|Spondylocarpotarsal_synostosis_syndrome": 1,
    "not_specified|Atelosteogenesis_type_III": 1,
    "Severe_postnatal_growth_retardation|Synostosis_involving_bones_of_the_lower_limbs": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Boomerang_dysplasia|FLNB-Related_Spectrum_Disorders|Atelosteogenesis_type_I|Larsen_syndrome|Atelosteogenesis_type_III|Spondylocarpotarsal_synostosis_syndrome|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|FLNB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|not_specified|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|not_provided": 2,
    "FLNB-Related_Spectrum_Disorders|Spondylocarpotarsal_synostosis_syndrome|Boomerang_dysplasia|Larsen_syndrome|Atelosteogenesis_type_I|Atelosteogenesis_type_III|not_specified|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|FLNB-related_disorder|not_provided|not_specified": 1,
    "not_provided|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome": 2,
    "not_provided|FLNB-related_disorder|FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder": 1,
    "not_provided|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|Atelosteogenesis_type_I|Boomerang_dysplasia|Atelosteogenesis_type_III": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|Inborn_genetic_diseases|FLNB-related_disorder|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|not_specified|not_provided|FLNB-related_disorder": 1,
    "Connective_tissue_disorder|not_specified|FLNB-Related_Spectrum_Disorders|not_provided": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|FLNB-related_disorder": 1,
    "Spondylocarpotarsal_synostosis_syndrome|FLNB-Related_Spectrum_Disorders|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Larsen_syndrome|Boomerang_dysplasia|not_provided": 1,
    "not_provided|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|FLNB-related_disorder": 1,
    "Boomerang_dysplasia|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|not_provided|FLNB-Related_Spectrum_Disorders": 1,
    "Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|FLNB-Related_Spectrum_Disorders|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Atelosteogenesis_type_I": 2,
    "Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|FLNB-related_disorder|not_provided": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|not_specified|Connective_tissue_disorder": 1,
    "not_specified|FLNB-related_disorder|FLNB-Related_Spectrum_Disorders|not_provided": 2,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Boomerang_dysplasia|Atelosteogenesis_type_I|Atelosteogenesis_type_III|Larsen_syndrome|Spondylocarpotarsal_synostosis_syndrome": 1,
    "FLNB-Related_Spectrum_Disorders|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Larsen_syndrome|Spondylocarpotarsal_synostosis_syndrome|FLNB-Related_Spectrum_Disorders|not_provided": 1,
    "FLNB-related_disorder|FLNB-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_provided|Connective_tissue_disorder": 1,
    "FLNB-related_disorder|not_specified|not_provided": 1,
    "not_provided|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Larsen_syndrome": 1,
    "Larsen_syndrome|not_specified|not_provided": 1,
    "Atelosteogenesis_type_III|Atelosteogenesis_type_I|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|Boomerang_dysplasia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_III|Larsen_syndrome|Atelosteogenesis_type_I|Boomerang_dysplasia": 1,
    "Boomerang_dysplasia|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome|FLNB-Related_Spectrum_Disorders": 1,
    "not_specified|Connective_tissue_disorder|FLNB-Related_Spectrum_Disorders|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|not_provided|not_specified|FLNB-related_disorder|Connective_tissue_disorder": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder": 1,
    "not_provided|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_I|Boomerang_dysplasia|Atelosteogenesis_type_III|Larsen_syndrome": 1,
    "Inborn_genetic_diseases|Larsen_syndrome|not_provided": 1,
    "Boomerang_dysplasia|Atelosteogenesis_type_I|Larsen_syndrome|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_III|not_provided": 1,
    "Larsen_syndrome|not_provided|Abnormality_of_the_skeletal_system": 1,
    "FLNB-Related_Spectrum_Disorders|not_specified|Inborn_genetic_diseases|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|not_provided|Skeletal_dysplasia": 1,
    "Patellar_hypoplasia|Knee_dislocation|Limited_knee_flexion/extension|not_provided": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|not_specified|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|not_provided": 1,
    "not_specified|not_provided|FLNB-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Connective_tissue_disorder": 3,
    "FLNB-Related_Spectrum_Disorders|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|not_provided": 1,
    "Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|not_specified|Connective_tissue_disorder|not_provided|FLNB-Related_Spectrum_Disorders": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|FLNB-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Atelosteogenesis_type_III": 1,
    "FLNB-related_disorder|Connective_tissue_disorder|FLNB-Related_Spectrum_Disorders|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|FLNB-Related_Spectrum_Disorders": 2,
    "not_specified|not_provided|Connective_tissue_disorder|Inborn_genetic_diseases|FLNB-related_disorder": 1,
    "FLNB-Related_Spectrum_Disorders|Connective_tissue_disorder|FLNB-related_disorder|Inborn_genetic_diseases|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|not_provided": 1,
    "not_provided|Boomerang_dysplasia|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I|Larsen_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|FLNB-Related_Spectrum_Disorders": 2,
    "Connective_tissue_disorder|Larsen_syndrome|not_provided|FLNB-Related_Spectrum_Disorders|not_specified": 1,
    "not_provided|Atelosteogenesis_type_III|Spondylocarpotarsal_synostosis_syndrome|Atelosteogenesis_type_I|Boomerang_dysplasia|Larsen_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|FLNB-related_disorder|FLNB-Related_Spectrum_Disorders": 1,
    "Atelosteogenesis_type_III|Spondylocarpotarsal_synostosis_syndrome|Larsen_syndrome": 1,
    "not_provided|FLNB-Related_Spectrum_Disorders|Inborn_genetic_diseases|FLNB-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Larsen_syndrome|Atelosteogenesis_type_III|Atelosteogenesis_type_I": 1,
    "Inborn_genetic_diseases|Atelosteogenesis_type_III|not_provided": 1,
    "not_provided|Autosomal_systemic_lupus_erythematosus_type_16": 20,
    "Inborn_genetic_diseases|Autosomal_systemic_lupus_erythematosus_type_16": 2,
    "Autosomal_systemic_lupus_erythematosus_type_16": 16,
    "Autosomal_systemic_lupus_erythematosus_type_16|not_provided": 23,
    "not_provided|Inborn_genetic_diseases|Autosomal_systemic_lupus_erythematosus_type_16": 1,
    "Autosomal_systemic_lupus_erythematosus_type_16|Inborn_genetic_diseases": 1,
    "Autosomal_systemic_lupus_erythematosus_type_16|not_provided|not_specified": 1,
    "DNASE1L3-related_disorder|not_provided": 2,
    "not_provided|not_specified|Autosomal_systemic_lupus_erythematosus_type_16": 1,
    "Autosomal_systemic_lupus_erythematosus_type_16|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_systemic_lupus_erythematosus_type_16|Inborn_genetic_diseases": 2,
    "DNASE1L3-related_disorder|Autosomal_systemic_lupus_erythematosus_type_16|not_provided": 1,
    "not_provided|DNASE1L3-related_disorder": 1,
    "Autosomal_systemic_lupus_erythematosus_type_16|not_specified|not_provided": 1,
    "DNASE1L3-related_disorder": 3,
    "Inborn_genetic_diseases|Autosomal_systemic_lupus_erythematosus_type_16|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_systemic_lupus_erythematosus_type_16": 1,
    "not_provided|Autosomal_systemic_lupus_erythematosus_type_16|not_specified": 1,
    "Pyruvate_dehydrogenase_complex_deficiency": 23,
    "Pyruvate_dehydrogenase_E1-beta_deficiency": 288,
    "not_provided|Pyruvate_dehydrogenase_E1-beta_deficiency": 11,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|not_provided": 4,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|Pyruvate_dehydrogenase_phosphatase_deficiency": 5,
    "Pyruvate_dehydrogenase_phosphatase_deficiency": 26,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-beta_deficiency|not_provided": 1,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 5,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency|not_provided": 1,
    "not_specified|Pyruvate_dehydrogenase_E1-beta_deficiency": 4,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|Pyruvate_dehydrogenase_complex_deficiency": 4,
    "Pyruvate_dehydrogenase_phosphatase_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 2,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-beta_deficiency|Pyruvate_dehydrogenase_phosphatase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|Pyruvate_dehydrogenase_complex_deficiency|not_provided": 1,
    "not_specified|not_provided|Pyruvate_dehydrogenase_phosphatase_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|not_specified": 5,
    "not_provided|Pyruvate_dehydrogenase_phosphatase_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "not_provided|not_specified|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "not_specified|not_provided|Pyruvate_dehydrogenase_E1-beta_deficiency": 2,
    "not_provided|Pyruvate_dehydrogenase_E1-beta_deficiency|not_specified|PDHB-related_disorder": 1,
    "not_specified|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency": 1,
    "Pyruvate_dehydrogenase_phosphatase_deficiency|Pyruvate_dehydrogenase_E1-beta_deficiency|not_provided": 1,
    "not_provided|Pyruvate_dehydrogenase_E1-beta_deficiency|Inborn_genetic_diseases": 1,
    "Pyruvate_dehydrogenase_E1-beta_deficiency|Inborn_genetic_diseases|Seizure": 1,
    "ACOX2-related_disorder": 26,
    "ACOX2-related_disorder|not_provided": 15,
    "Congenital_bile_acid_synthesis_defect_6": 6,
    "not_provided|ACOX2-related_disorder": 12,
    "ACOX2-related_disorder|Congenital_bile_acid_synthesis_defect_6|not_provided": 2,
    "ACOX2-related_disorder|not_provided|not_specified": 2,
    "ACOX2-related_disorder|not_specified": 2,
    "Congenital_bile_acid_synthesis_defect_6|not_provided": 2,
    "ACOX2-related_disorder|Congenital_bile_acid_synthesis_defect_6|not_provided|not_specified": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_6": 3,
    "not_provided|not_specified|ACOX2-related_disorder": 1,
    "Familial_ovarian_cancer": 23,
    "FHIT-related_disorder": 2,
    "FEZF2-related_neurodevelopmental_condition": 1,
    "FEZF2-related_disorder": 4,
    "Hypomyelination_and_Congenital_Cataract": 248,
    "Neurodevelopmental_phenotype": 1,
    "not_provided|FEZF2-related_disorder": 2,
    "CADPS-related_disorder": 32,
    "CADPS-related_disorder|not_specified": 1,
    "CADPS-related_disorder|not_provided": 2,
    "not_provided|CADPS-related_disorder": 1,
    "ATXN7-related_disorder": 6,
    "Retinal_dystrophy|ATXN7-related_disorder": 1,
    "Spinocerebellar_ataxia_7": 7,
    "Abnormality_of_neuronal_migration|not_provided": 1,
    "not_provided|ATXN7-related_disorder": 1,
    "Inborn_genetic_diseases|ATXN7-related_disorder": 1,
    "Spinocerebellar_ataxia_7|Inborn_genetic_diseases": 1,
    "not_specified|ATXN7-related_disorder|not_provided": 1,
    "Progressive_myoclonic_epilepsy": 822,
    "Progressive_myoclonic_epilepsy|not_provided": 64,
    "Progressive_myoclonic_epilepsy_type_5": 352,
    "Progressive_myoclonic_epilepsy_type_5|not_specified": 23,
    "not_provided|not_specified|Progressive_myoclonic_epilepsy_type_5": 1,
    "not_provided|Progressive_myoclonic_epilepsy_type_5": 7,
    "Myoclonic_epilepsy|not_specified|Progressive_myoclonic_epilepsy_type_5": 1,
    "Progressive_myoclonic_epilepsy_type_5|not_provided|not_specified": 1,
    "Progressive_myoclonic_epilepsy_type_5|Progressive_myoclonic_epilepsy": 5,
    "PRICKLE2-related_disorder": 4,
    "PRICKLE2-related_disorder|Progressive_myoclonic_epilepsy_type_5|not_provided": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_5": 15,
    "Progressive_myoclonic_epilepsy|not_provided|Progressive_myoclonic_epilepsy_type_5": 1,
    "Progressive_myoclonic_epilepsy_type_5|not_provided": 7,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy_type_5": 1,
    "Progressive_myoclonic_epilepsy_type_5|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided|not_specified": 1,
    "Myoclonic_epilepsy": 1,
    "PRICKLE2-associated_epilepsy_syndrome": 1,
    "Progressive_myoclonic_epilepsy|Progressive_myoclonic_epilepsy_type_5": 7,
    "Progressive_myoclonic_epilepsy_type_5|PRICKLE2-related_disorder|not_specified|not_provided|Progressive_myoclonic_epilepsy": 1,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy_type_5|PRICKLE2-related_disorder|Progressive_myoclonic_epilepsy": 1,
    "Progressive_myoclonic_epilepsy|Self-limited_epilepsy_with_centrotemporal_spikes|Progressive_myoclonic_epilepsy_type_5|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_5|not_specified|not_provided": 2,
    "PRICKLE2-related_disorder|Progressive_myoclonic_epilepsy_type_5": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_5|Progressive_myoclonic_epilepsy": 2,
    "not_provided|Progressive_myoclonic_epilepsy_type_5|not_specified": 3,
    "not_specified|Progressive_myoclonic_epilepsy_type_5|not_provided|Progressive_myoclonic_epilepsy": 2,
    "Progressive_myoclonic_epilepsy_type_5|PRICKLE2-related_disorder": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_5|Progressive_myoclonic_epilepsy|not_provided": 2,
    "PRICKLE2-associated_neurodevelopmental_disorder": 1,
    "Autosomal_dominant_non-syndromic_intellectual_disability": 7,
    "Progressive_myoclonic_epilepsy_type_5|Progressive_myoclonic_epilepsy|not_specified": 2,
    "Progressive_myoclonic_epilepsy|not_specified": 21,
    "Myoclonic_epilepsy|_progressive|_X-linked|Progressive_myoclonic_epilepsy|not_provided|not_specified|Progressive_myoclonic_epilepsy_type_5": 1,
    "Progressive_myoclonic_epilepsy|Progressive_myoclonic_epilepsy_type_5|not_provided|not_specified": 1,
    "Progressive_myoclonic_epilepsy_type_5|PRICKLE2-related_disorder|not_provided|not_specified": 1,
    "PRICKLE2-related_neurodevelopmental_disorder": 1,
    "not_provided|Progressive_myoclonic_epilepsy|Progressive_myoclonic_epilepsy_type_5": 1,
    "not_provided|Progressive_myoclonic_epilepsy": 38,
    "ADAMTS9-related_disorder|not_provided": 14,
    "not_provided|ADAMTS9-related_disorder": 16,
    "ADAMTS9-related_disorder": 9,
    "ADAMTS9-related_disorder|not_specified": 1,
    "not_provided|ADAMTS9-related_disorder|not_specified": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_28": 5,
    "SLC25A26-related_disorder": 2,
    "not_provided|SLC25A26-related_disorder": 2,
    "not_provided|SLC25A26-related_disorder|Combined_oxidative_phosphorylation_deficiency_28": 1,
    "Combined_oxidative_phosphorylation_deficiency_28": 8,
    "SLC25A26-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_28|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|LRIG1-related_disorder": 1,
    "LRIG1-related_disorder": 34,
    "LRIG1-related_disorder|not_provided": 5,
    "LRIG1-related_disorder|not_provided|not_specified": 4,
    "not_provided|LRIG1-related_disorder": 6,
    "LRIG1-related_disorder|not_specified|not_provided": 1,
    "not_specified|LRIG1-related_disorder": 1,
    "SUCLG2-related_disorder|not_provided": 2,
    "SUCLG2-related_disorder": 3,
    "not_provided|SUCLG2-related_disorder": 3,
    "Inborn_genetic_diseases|Adams-Oliver_syndrome_4": 7,
    "Adams-Oliver_syndrome_4": 101,
    "EOGT-related_disorder": 3,
    "Adams-Oliver_syndrome_4|Inborn_genetic_diseases": 3,
    "Adams-Oliver_syndrome_4|not_provided": 12,
    "EOGT-related_disorder|Adams-Oliver_syndrome_4": 1,
    "Adams-Oliver_syndrome_4|Adams-Oliver_syndrome|not_provided": 1,
    "Adams-Oliver_syndrome_4|EOGT-related_disorder": 1,
    "not_provided|EOGT-related_disorder|Adams-Oliver_syndrome_4": 1,
    "not_provided|Adams-Oliver_syndrome_4": 3,
    "not_specified|Adams-Oliver_syndrome_4": 1,
    "Adams-Oliver_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Adams-Oliver_syndrome_4": 1,
    "Nemaline_myopathy_10": 285,
    "Nemaline_myopathy_10|not_provided": 27,
    "Nemaline_myopathy_10|Inborn_genetic_diseases": 14,
    "Nemaline_myopathy_10|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Nemaline_myopathy_10": 1,
    "not_provided|Nemaline_myopathy_10": 10,
    "LMOD3-related_disorder|Nemaline_myopathy_10": 5,
    "Inborn_genetic_diseases|Nemaline_myopathy_10": 28,
    "LMOD3-related_disorder": 2,
    "LMOD3-related_disorder|Nemaline_myopathy_10|Inborn_genetic_diseases|not_provided": 1,
    "Nemaline_myopathy_10|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Nemaline_myopathy_10": 1,
    "Nemaline_myopathy_10|Inborn_genetic_diseases|not_provided|LMOD3-related_disorder": 1,
    "Nemaline_myopathy_10|Inborn_genetic_diseases|not_provided": 1,
    "Nemaline_myopathy_10|LMOD3-related_disorder|not_provided": 1,
    "Nemaline_myopathy_10|not_specified|not_provided|Joubert_syndrome_24": 1,
    "Nemaline_myopathy_10|not_provided|LMOD3-related_disorder|not_specified": 1,
    "LMOD3-related_disorder|Nemaline_myopathy_10|Inborn_genetic_diseases": 1,
    "Nemaline_myopathy_10|not_provided|not_specified": 2,
    "Nemaline_myopathy_10|LMOD3-related_disorder": 2,
    "Nemaline_myopathy_10|not_provided|Inborn_genetic_diseases": 1,
    "Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 5,
    "MITF-related_disorder": 21,
    "Tietz_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|MITF-related_disorder|not_specified": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "MITF-related_disorder|not_provided": 5,
    "MITF-related_disorder|not_specified|not_provided": 1,
    "MITF-related_disorder|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|not_provided": 1,
    "not_specified|MITF-related_disorder": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A": 41,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_provided": 1,
    "not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 170,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided": 11,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 147,
    "MITF-related_disorder|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 3,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 14,
    "Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 14,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome": 43,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome": 8,
    "Waardenburg_syndrome_type_2A": 67,
    "Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome": 6,
    "Waardenburg_syndrome_type_2A|Waardenburg_syndrome_type_2|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 14,
    "not_specified|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "MITF-related_disorder|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_specified|not_provided": 1,
    "not_provided|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome": 4,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome": 4,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome": 14,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|MITF-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 20,
    "Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Hereditary_cancer-predisposing_syndrome": 7,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder": 1,
    "Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|not_provided": 5,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 3,
    "MITF-related_disorder|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 6,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|MITF-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 6,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder|not_provided": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome": 4,
    "MITF-related_disorder|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder|not_provided": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 3,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified": 2,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome": 1,
    "Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A": 13,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|MITF-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome": 1,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Hereditary_cancer-predisposing_syndrome": 1,
    "MITF-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome|not_specified": 1,
    "Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Tietz_syndrome|not_provided": 1,
    "not_provided|not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|not_provided": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided": 4,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_provided": 5,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_specified": 2,
    "not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "MITF-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 3,
    "MITF-related_disorder|not_specified|not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder|not_provided": 1,
    "Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_provided|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness": 1,
    "not_provided|Anophthalmia-microphthalmia_syndrome": 19,
    "Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Oculocutaneous_albinism_type_4|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness": 1,
    "Tietz_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome|not_provided|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|not_provided|not_specified": 1,
    "not_provided|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|MITF-related_disorder": 1,
    "not_provided|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Tietz_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome": 21,
    "not_provided|Waardenburg_syndrome_type_2": 1,
    "Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Waardenburg_syndrome_type_2A": 2,
    "Waardenburg_syndrome_type_2A|Intellectual_disability|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder": 1,
    "Waardenburg_syndrome_type_2A|Heterochromia_iridis|Prelingual_sensorineural_hearing_impairment|Poliosis|Hearing_impairment|not_provided|Ear_malformation": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Waardenburg_syndrome|Monogenic_hearing_loss|not_provided": 1,
    "not_provided|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome": 2,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|MITF-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Waardenburg_syndrome_type_2A|MITF-related_disorder|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Waardenburg_syndrome_type_2A|MITF-related_disorder": 1,
    "not_provided|Waardenburg_syndrome_type_2A": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Tietz_syndrome|Waardenburg_syndrome_type_2A|Nonsyndromic_Deafness|not_provided": 1,
    "Waardenburg_syndrome_type_2A|not_provided|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_1": 1,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Familial_melanoma": 1,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|MITF-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder|not_provided": 1,
    "Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|MITF-related_disorder": 1,
    "not_specified|Waardenburg_syndrome_type_2A|Tietz_syndrome|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|MITF-related_disorder": 1,
    "MITF-related_disorder|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Congenital_sensorineural_hearing_impairment|not_provided": 1,
    "Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|not_provided": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome|Waardenburg_syndrome_type_2|not_provided|Rare_genetic_deafness": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|MITF-related_disorder": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified|not_provided": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|not_provided|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_provided|MITF-related_disorder": 1,
    "not_provided|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|MITF-related_disorder": 1,
    "not_specified|MITF-related_disorder|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2|not_provided": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified": 1,
    "MITF-related_disorder|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided": 1,
    "Waardenburg_syndrome|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|not_specified|not_provided|MITF-related_disorder": 1,
    "not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Waardenburg_syndrome_type_2A|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A|MITF-related_disorder": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome|MITF-related_disorder|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Melanoma|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Tietz_syndrome|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|MITF-related_disorder": 1,
    "not_specified|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|MITF-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|not_specified|not_provided|MITF-related_disorder": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|MITF-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|not_provided|Tietz_syndrome|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness": 1,
    "MITF-related_disorder|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tietz_syndrome|not_provided|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome|MITF-related_disorder": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|MITF-related_disorder": 1,
    "Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome|Coloboma|_osteopetrosis|_microphthalmia|_macrocephaly|_albinism|_and_deafness|not_provided": 1,
    "MITF-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Hereditary_cancer-predisposing_syndrome|Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_specified": 1,
    "not_specified|MITF-related_disorder|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Waardenburg_syndrome_type_2A|Tietz_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "not_provided|MITF-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|Waardenburg_syndrome_type_2A": 1,
    "Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|MITF-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tietz_syndrome|Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_8|not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Waardenburg_syndrome_type_2A|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Tietz_syndrome|not_specified|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Waardenburg_syndrome_type_2A|Tietz_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Waardenburg_syndrome_type_2A|Tietz_syndrome|MITF-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_8": 1,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Waardenburg_syndrome_type_2A|not_provided|Tietz_syndrome": 6,
    "Waardenburg_syndrome|Tietz_syndrome": 6,
    "Tietz_syndrome|not_provided|Waardenburg_syndrome_type_2A": 1,
    "not_provided|Tietz_syndrome|Waardenburg_syndrome_type_2A": 2,
    "Waardenburg_syndrome|not_provided|Tietz_syndrome": 1,
    "Intellectual_Disability_with_Language_Impairment_and_Autistic_Features|not_provided": 11,
    "Intellectual_Disability_with_Language_Impairment_and_Autistic_Features": 36,
    "not_provided|Intellectual_Disability_with_Language_Impairment_and_Autistic_Features": 2,
    "Inborn_genetic_diseases|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|not_provided": 2,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 113,
    "not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|Inborn_genetic_diseases": 2,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|not_provided": 12,
    "not_specified|not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 1,
    "FOXP1-related_disorder": 15,
    "not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 12,
    "Atrial_septal_defect_1|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|FOXP1-related_disorder": 1,
    "Inborn_genetic_diseases|FOXP1-related_disorder|not_specified|not_provided": 1,
    "FOXP1-related_disorder|Inborn_genetic_diseases|Mitral_atresia_disorder|Hypoplastic_left_heart_syndrome_1|Aortic_valve_atresia|Single_Ventricle_Defect|Visceral_heterotaxy|Pulmonary_atresia_with_ventricular_septal_defect|Familial_atrioventricular_septal_defect|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 1,
    "FOXP1-related_disorder|not_provided": 14,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided": 16,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|Intellectual_disability|Seizure|Rare_genetic_intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 3,
    "INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AND_AUTISTIC_FEATURES|not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|See_cases|Intellectual_disability": 1,
    "not_provided|FOXP1-related_disorder|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AND_AUTISTIC_FEATURES": 1,
    "FOXP1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Intellectual_disability|Anterior_creases_of_earlobe|Delayed_speech_and_language_development|Strabismus|Glabellar_hemangioma": 1,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AND_AUTISTIC_FEATURES|Intellectual_disability": 1,
    "Intellectual_disability|Autism": 1,
    "not_provided|FOXP1-related_disorder": 2,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_LANGUAGE_IMPAIRMENT_AND_AUTISTIC_FEATURES": 1,
    "not_provided|Autism_spectrum_disorder|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 1,
    "Congenital_heart_disease|not_provided": 4,
    "FOXP1-related_disorder|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|not_provided": 1,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_disorder|not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome": 1,
    "not_provided|FOXP1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "FOXP1-related_disorder|not_provided|not_specified": 1,
    "FOXP1-related_disorder|not_specified|not_provided": 2,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|Cerebellar_vermis_hypoplasia|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|FOXP1-related_disorder": 1,
    "not_specified|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|not_provided": 1,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|not_provided|FOXP1-related_disorder": 1,
    "FOXP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "FOXP1-related_disorder|Intellectual_disability-severe_speech_delay-mild_dysmorphism_syndrome|Cerebellar_vermis_hypoplasia|Inborn_genetic_diseases|not_specified|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "PROK2-related_disorder": 21,
    "Hypogonadotropic_hypogonadism_4_with_or_without_anosmia": 2,
    "Inborn_genetic_diseases|PROK2-related_disorder": 3,
    "Male_infertility_with_spermatogenesis_disorder": 8,
    "not_provided|PROK2-related_disorder": 2,
    "not_provided|Hypogonadotropic_hypogonadism_4_with_or_without_anosmia|PROK2-related_disorder|not_specified": 2,
    "PROK2-related_disorder|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_4_with_or_without_anosmia": 1,
    "PROK2-related_disorder|not_provided": 2,
    "PROK2-related_disorder|not_provided|Hypogonadotropic_hypogonadism_4_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_4_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_4_with_or_without_anosmia|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|PROK2-related_disorder|not_provided": 1,
    "Hypogonadotropic_hypogonadism_4_with_or_without_anosmia|PROK2-related_disorder": 2,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_4_with_or_without_anosmia": 1,
    "RYBP-related_condition": 2,
    "SHQ1-related_disorder": 2,
    "Neurodevelopmental_disorder_with_dystonia_and_seizures": 3,
    "Neurodevelopmental_disorder_with_dystonia_and_seizures|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_dystonia_and_seizures": 1,
    "SHQ1-related_disorder|Dystonia_35|_childhood-onset|Neurodevelopmental_disorder_with_dystonia_and_seizures|not_provided": 1,
    "Dystonia_35|_childhood-onset|not_provided": 1,
    "CNTN3-related_disorder": 14,
    "CNTN3-related_disorder|not_provided": 4,
    "not_provided|CNTN3-related_disorder": 1,
    "CNTN3-related_disorder|not_specified": 1,
    "Prostate_cancer|not_provided": 9,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)": 2,
    "ROBO2-related_disorder": 17,
    "ROBO2-related_disorder|Vesicoureteral_reflux_2": 2,
    "not_provided|Vesicoureteral_reflux_2": 42,
    "Vesicoureteral_reflux_2": 198,
    "Vesicoureteral_reflux_2|not_provided": 11,
    "not_provided|ROBO2-related_disorder|Vesicoureteral_reflux_2": 2,
    "Inborn_genetic_diseases|ROBO2-related_disorder": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Vesicoureteral_reflux_2": 6,
    "not_provided|ROBO2-related_disorder": 6,
    "ROBO2-related_disorder|not_provided|Vesicoureteral_reflux_2": 4,
    "Vesicoureteral_reflux_2|Inborn_genetic_diseases": 11,
    "ROBO2-related_disorder|not_provided": 3,
    "Vesicoureteral_reflux_2|ROBO2-related_disorder": 2,
    "Vesicoureteral_reflux_2|not_specified|not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "ROBO2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Vesicoureteral_reflux_2|not_provided": 3,
    "Inborn_genetic_diseases|Vesicoureteral_reflux_2": 8,
    "not_provided|Vesicoureteral_reflux_2|ROBO2-related_disorder": 4,
    "Inborn_genetic_diseases|Congenital_anomaly_of_kidney_and_urinary_tract|Vesicoureteral_reflux_2": 1,
    "Vesicoureteral_reflux|not_provided": 2,
    "ROBO2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 2,
    "Inborn_genetic_diseases|not_provided|Vesicoureteral_reflux_2": 2,
    "Vesicoureteral_reflux_2|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "ROBO2-related_disorder|Vesicoureteral_reflux_2|not_provided": 1,
    "Vesicoureteral_reflux_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Vesicoureteral_reflux_2|ROBO2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Vesicoureteral_reflux_2|Inborn_genetic_diseases": 1,
    "Vesicoureteral_reflux_2|Inborn_genetic_diseases|ROBO2-related_disorder": 1,
    "Vesicoureteral_reflux_2|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Vesicoureteral_reflux_2|ROBO2-related_disorder|not_provided": 1,
    "Vesicoureteral_reflux_2|not_specified": 1,
    "Vesicoureteral_reflux": 7,
    "not_provided|Vesicoureteral_reflux": 1,
    "ROBO1-related_disorder": 22,
    "Neurooculorenal_syndrome|Bilateral_renal_agenesis": 2,
    "not_provided|ROBO1-related_disorder": 17,
    "not_provided|ROBO1-related_disorder|Inborn_genetic_diseases": 2,
    "Heart|_malformation_of": 19,
    "ROBO1-related_disorder|not_provided": 11,
    "Pituitary_hormone_deficiency|_combined_or_isolated|_8": 2,
    "Congenital_nystagmus|Nystagmus|_congenital|_autosomal_recessive|not_provided": 1,
    "Neurooculorenal_syndrome": 3,
    "ROBO1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "ROBO1-related_disorder|not_provided|Heart|_malformation_of": 1,
    "Nystagmus|_congenital|_autosomal_recessive|not_provided": 1,
    "Neurooculorenal_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract": 3,
    "Inborn_genetic_diseases|Congenital_anomaly_of_kidney_and_urinary_tract": 2,
    "Neurodevelopmental_delay|ROBO1-related_disorder|not_provided": 1,
    "Increased_nuchal_translucency": 1,
    "Pituitary_hormone_deficiency|_combined_or_isolated|_8|Pituitary_stalk_interruption_syndrome": 2,
    "Inborn_genetic_diseases|Imperforate_anus|Short_stature|Ectopic_posterior_pituitary|Central_hypothyroidism|Hypopituitarism|Abnormal_growth_hormone_level": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Neurooculorenal_syndrome": 1,
    "Neurooculorenal_syndrome|Nystagmus|_congenital|_autosomal_recessive|ROBO1-related_disorder": 1,
    "Tetralogy_of_Fallot|not_provided": 2,
    "ROBO1-related_disorder|Inborn_genetic_diseases": 1,
    "Tetralogy_of_Fallot|Neurooculorenal_syndrome": 1,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV": 24,
    "Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease": 13,
    "Adult_polyglucosan_body_disease|not_provided|Glycogen_storage_disease|_type_IV": 2,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|not_provided": 1,
    "Glycogen_storage_disease|_type_IV": 90,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_specified|not_provided": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 261,
    "not_provided|Polyneuropathy": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV": 359,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|not_provided": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_provided": 10,
    "GBE1-related_disorder|not_provided|Glycogen_storage_disease|_type_IV|See_cases|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "not_specified|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV": 4,
    "not_provided|GBE1-related_disorder|Glycogen_storage_disease|_type_IV": 1,
    "Adult_polyglucosan_body_disease|not_provided|Adult_polyglucosan_body_neuropathy": 1,
    "GBE1-related_disorder": 5,
    "not_provided|Glycogen_storage_disease|_type_IV": 3,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease": 7,
    "not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 8,
    "not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease": 3,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|not_specified|not_provided": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_provided": 4,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Inborn_genetic_diseases": 8,
    "GBE1-related_disorder|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 3,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease|not_provided|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_childhood_neuromuscular_form": 2,
    "GBE1-related_disorder|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV": 1,
    "Glycogen_storage_disease|_type_IV|not_provided": 4,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_provided|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta_type_15": 16,
    "Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|Glycogen_storage_disease_IV|_classic_hepatic": 3,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|GBE1-related_disorder|Adult_polyglucosan_body_disease|not_provided|not_specified": 1,
    "Glycogen_storage_disease|_type_IV|Inborn_genetic_diseases|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|GBE1-related_disorder": 6,
    "not_provided|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV": 3,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease|not_provided": 4,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_congenital_neuromuscular_form": 2,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_provided|Inborn_genetic_diseases": 1,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|not_specified|not_provided|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_specified|not_provided|Adult_polyglucosan_body_disease|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_congenital_neuromuscular_form": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_specified|not_provided": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_fatal_perinatal_neuromuscular_form": 1,
    "not_specified|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 6,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 4,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|GBE1-related_disorder|Adult_polyglucosan_body_disease": 1,
    "GBE1-related_disorder|Adult_polyglucosan_body_disease|not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease_IV|_combined_hepatic_and_myopathic|Adult_polyglucosan_body_neuropathy": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 3,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_neuropathy|GBE1-related_disorder|not_provided|Adult_polyglucosan_body_disease|See_cases": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Inborn_genetic_diseases|not_provided": 2,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_specified|not_provided|Adult_polyglucosan_body_disease": 1,
    "not_specified|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_provided": 1,
    "Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|not_provided|Dementia|Glycogen_storage_disease_IV|_classic_hepatic|GBE1-related_disorder": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1B": 190,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease": 1,
    "not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease|_type_IV|not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 2,
    "GBE1-related_disorder|not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "not_specified|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease": 1,
    "GBE1-related_disorder|not_specified|Glycogen_storage_disease|_type_IV": 1,
    "Glycogen_storage_disease|_type_IV|Inborn_genetic_diseases": 2,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|GBE1-related_disorder|not_provided|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Arthrogryposis_syndrome|not_specified": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Inborn_genetic_diseases|not_provided": 2,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_specified|not_provided|Adult_polyglucosan_body_disease": 2,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_IV": 2,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|not_provided|GBE1-related_disorder|not_specified|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Adult_polyglucosan_body_neuropathy|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Inborn_genetic_diseases|GBE1-related_disorder|Adult_polyglucosan_body_disease|not_provided|Glycogen_storage_disease_IV|_nonprogressive_hepatic": 1,
    "Adult_polyglucosan_body_disease": 1,
    "not_provided|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "not_provided|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_specified": 1,
    "not_specified|not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease": 1,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_congenital_neuromuscular_form": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_congenital_neuromuscular_form": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease|not_specified|not_provided": 1,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|GBE1-related_disorder|not_provided": 1,
    "not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Arthrogryposis_syndrome|GBE1-related_disorder|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|GBE1-related_disorder|Adult_polyglucosan_body_disease|not_provided|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_congenital_neuromuscular_form": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_congenital_neuromuscular_form": 1,
    "GBE1-related_disorder|Arthrogryposis_syndrome|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Inborn_genetic_diseases|Adult_polyglucosan_body_disease|not_provided|Glycogen_storage_disease|Dementia": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_nonprogressive_hepatic|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_neuropathy|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease|Inborn_genetic_diseases": 1,
    "Adult_polyglucosan_body_disease|GBE1-related_disorder|not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "not_provided|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|not_specified|Glycogen_storage_disease_IV|_classic_hepatic": 3,
    "not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_specified|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease|_type_IV|GBE1-related_disorder|Adult_polyglucosan_body_disease|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_specified": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|GBE1-related_disorder|not_provided": 1,
    "not_provided|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|See_cases": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_provided|Adult_polyglucosan_body_disease": 2,
    "Adult_polyglucosan_body_disease|Inborn_genetic_diseases|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_provided": 1,
    "not_specified|not_provided|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_provided|GBE1-related_disorder": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_provided": 1,
    "not_specified|GBE1-related_disorder|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|GBE1-related_disorder": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|not_specified": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease|not_specified": 1,
    "not_provided|not_specified|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV": 1,
    "not_provided|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Adult_polyglucosan_body_disease|not_specified": 1,
    "GBE1-related_disorder|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_specified": 1,
    "Glycogen_storage_disease_due_to_glycogen_branching_enzyme_deficiency|_fatal_perinatal_neuromuscular_form|Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic": 1,
    "GBE1-related_disorder|Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|Adult_polyglucosan_body_disease|not_provided|not_specified": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_provided|not_specified|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease_IV|_combined_hepatic_and_myopathic": 1,
    "Glycogen_storage_disease_IV|_classic_hepatic|Glycogen_storage_disease|_type_IV|not_provided|GBE1-related_disorder|Adult_polyglucosan_body_disease": 1,
    "Glycogen_storage_disease|_type_IV|Glycogen_storage_disease_IV|_classic_hepatic|Inborn_genetic_diseases|not_provided|Adult_polyglucosan_body_disease": 1,
    "Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|GBE1-related_disorder|not_specified|Glycogen_storage_disease_IV|_classic_hepatic|not_provided": 1,
    "not_provided|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV|not_specified": 1,
    "Glycogen_storage_disease|_type_IV|not_provided|Adult_polyglucosan_body_disease": 1,
    "not_provided|Adult_polyglucosan_body_disease|Glycogen_storage_disease|_type_IV": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|not_provided": 10,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 4,
    "CHMP2B-related_disorder": 8,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|not_specified": 1,
    "not_provided|CHMP2B-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 4,
    "CHMP2B-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 3,
    "CHMP2B-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|not_provided": 1,
    "CHMP2B-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|not_specified": 1,
    "not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|CHMP2B-related_disorder": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|CHMP2B-related_disorder": 3,
    "Amyotrophic_lateral_sclerosis|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|CHMP2B-related_disorder|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|not_specified|CHMP2B-related_disorder": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|not_specified": 1,
    "CHMP2B-related_disorder|not_specified": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 4,
    "Parkinsonian_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|Inborn_genetic_diseases": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7|Frontotemporal_dementia": 2,
    "Frontotemporal_dementia|Combined_Pituitary_Hormone_Deficiency|_Recessive|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_7": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|Pituitary_hormone_deficiency|_combined|_1": 2,
    "Frontotemporal_dementia|Pituitary_hormone_deficiency|_combined|_1|not_provided": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive": 4,
    "Frontotemporal_dementia|Combined_Pituitary_Hormone_Deficiency|_Recessive|Pituitary_hormone_deficiency|_combined|_1|not_provided": 3,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|Frontotemporal_dementia": 1,
    "not_provided|Pituitary_hormone_deficiency|_combined|_1": 5,
    "not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form": 4,
    "Pituitary_hormone_deficiency|_combined|_1|not_provided": 8,
    "Leber_congenital_amaurosis_5": 134,
    "POU1F1-related_disorder|not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form|Pituitary_hormone_deficiency|_combined|_1": 1,
    "Frontotemporal_dementia|Pituitary_hormone_deficiency|_combined|_1|Combined_Pituitary_Hormone_Deficiency|_Recessive|not_provided|not_specified": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|not_provided|Frontotemporal_dementia": 1,
    "Pituitary_hormone_deficiency|_combined|_1|not_provided|POU1F1-related_disorder": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|not_specified|not_provided": 1,
    "Pituitary_hormone_deficiency|_combined|_1|POU1F1-related_disorder|Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided": 1,
    "Pituitary_hormone_deficiency|_combined|_1|not_specified": 3,
    "not_provided|POU1F1-related_disorder": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|Pituitary_hormone_deficiency|_combined|_1|not_provided": 1,
    "not_provided|not_specified|Pituitary_hormone_deficiency|_combined|_1": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|Pituitary_hormone_deficiency|_combined|_1": 1,
    "Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_1|Combined_pituitary_hormone_deficiencies|_genetic_form": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|POU1F1-related_disorder|Pituitary_hormone_deficiency|_combined|_1|not_specified|not_provided": 1,
    "Combined_Pituitary_Hormone_Deficiency|_Recessive|not_provided": 2,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided": 3,
    "POU1F1-related_disorder": 3,
    "Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_1": 1,
    "Inborn_genetic_diseases|not_provided|Pituitary_hormone_deficiency|_combined|_1": 1,
    "not_provided|Pituitary_hormone_deficiency|_combined|_1|POU1F1-related_disorder": 1,
    "EPHA3-related_disorder": 11,
    "EPHA3-related_disorder|not_provided": 4,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 74,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 10,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 2,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|not_provided": 2,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 28,
    "Protein_S_deficiency_disease|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 5,
    "PROS1-related_disorder": 7,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 259,
    "not_provided|not_specified|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 2,
    "Protein_S_deficiency_disease": 18,
    "PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 2,
    "Protein_S_deficiency_disease|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 2,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Optic_atrophy": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|not_provided": 6,
    "Hereditary_thrombophilia_due_to_congenital_protein_S_deficiency|Protein_S_deficiency_disease": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|PROS1-related_disorder": 2,
    "Retinal_dystrophy|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 3,
    "Protein_S_deficiency_disease|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "PROS1-related_disorder|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Protein_S_deficiency_disease|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|PROS1-related_disorder": 1,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|PROS1-related_disorder|Protein_S_deficiency_disease|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Hereditary_thrombophilia_due_to_congenital_protein_S_deficiency|Optic_atrophy|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Retinal_dystrophy|not_provided|Protein_S_Heerlen|not_specified": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|PROS1-related_disorder|Protein_S_deficiency_disease": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|not_provided": 2,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease": 1,
    "Inborn_genetic_diseases|PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|PROS1-related_disorder": 7,
    "Protein_S_deficiency_disease|PROS1-related_disorder|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Protein_S_deficiency_disease|PROS1-related_disorder": 1,
    "Abnormal_thrombosis": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Protein_S_deficiency_disease": 2,
    "not_provided|PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Retinal_dystrophy|not_provided": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|not_provided": 1,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Incidental_Discovery": 1,
    "Finnish_congenital_nephrotic_syndrome|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Retinal_dystrophy|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease|PROS1-related_disorder": 1,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 3,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Hereditary_thrombophilia_due_to_congenital_protein_S_deficiency|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "PROS1-related_disorder|Retinal_dystrophy|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Protein_S_deficiency_disease|PROS1-related_disorder": 1,
    "not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease|Thrombocytopenia|Abnormal_bleeding": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|PROS1-related_disorder|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease|Deep_venous_thrombosis|PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|not_provided": 1,
    "Retinal_dystrophy|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "Abnormal_bleeding|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease": 2,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thromboembolism": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease|PROS1-related_disorder": 1,
    "Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant": 1,
    "PROS1-related_disorder|not_provided|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|Protein_S_deficiency_disease": 1,
    "not_provided|Protein_S_deficiency_disease": 1,
    "PROS1-related_disorder|Thrombophilia_due_to_protein_S_deficiency|_autosomal_recessive|Thrombophilia_due_to_protein_S_deficiency|_autosomal_dominant|not_provided": 1,
    "Joubert_syndrome_8|not_provided": 8,
    "Joubert_syndrome_8": 246,
    "ARL13B-related_disorder|not_provided|Joubert_syndrome_8": 3,
    "Joubert_syndrome_8|ARL13B-related_disorder": 1,
    "not_specified|not_provided|Joubert_syndrome_8": 2,
    "Joubert_syndrome_8|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Joubert_syndrome_8": 3,
    "ARL13B-related_disorder": 7,
    "not_provided|Joubert_syndrome_8": 6,
    "Inborn_genetic_diseases|Joubert_syndrome_8": 10,
    "Joubert_syndrome_8|Joubert_syndrome_and_related_disorders": 3,
    "Joubert_syndrome_8|Inborn_genetic_diseases": 15,
    "Joubert_syndrome_8|Long_QT_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_8": 1,
    "not_specified|Inborn_genetic_diseases|Joubert_syndrome_8": 1,
    "not_provided|Joubert_syndrome_1": 7,
    "Joubert_syndrome_8|Joubert_syndrome_1": 1,
    "ARL13B-related_disorder|Joubert_syndrome_8": 2,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_8|not_provided": 1,
    "not_provided|Joubert_syndrome_8|Inborn_genetic_diseases": 2,
    "Joubert_syndrome_8|not_specified|not_provided": 1,
    "not_specified|Joubert_syndrome_8|ARL13B-related_disorder": 1,
    "Joubert_syndrome_8|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_8|ARL13B-related_disorder|not_provided": 1,
    "not_specified|Joubert_syndrome_1|not_provided|Joubert_syndrome_8": 1,
    "Joubert_syndrome_8|not_specified": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|not_provided|Joubert_syndrome_8": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_8": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_8|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_48": 4,
    "NSUN3-related_disorder": 2,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_48": 2,
    "Combined_oxidative_phosphorylation_deficiency_48|not_provided": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_3": 7,
    "Bardet-Biedl_syndrome|Retinitis_Pigmentosa|_Recessive": 2,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa": 7,
    "Bardet-Biedl_syndrome_3": 6,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|Bardet-Biedl_syndrome_1": 9,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55": 66,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|ARL6-related_disorder": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55": 3,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3": 63,
    "ARL6-related_disorder|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55": 9,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|ARL6-related_disorder": 7,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Inborn_genetic_diseases|ARL6-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|not_provided|Bardet-Biedl_syndrome_1": 1,
    "ARL6-related_disorder": 19,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|not_provided|Bardet-Biedl_syndrome_1|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|ARL6-related_disorder": 3,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa|ARL6-related_disorder|Retinitis_pigmentosa_55": 1,
    "Inborn_genetic_diseases|ARL6-related_disorder|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1|ARL6-related_disorder": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|not_provided|not_specified": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3": 1,
    "Retinitis_pigmentosa_55": 2,
    "ARL6-related_disorder|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa|ARL6-related_disorder": 1,
    "Retinitis_pigmentosa|not_provided|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_55": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|not_provided": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|ARL6-related_disorder|Bardet-Biedl_syndrome_1|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|not_specified": 20,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Retinal_dystrophy|Inborn_genetic_diseases|ARL6-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55": 2,
    "Retinal_dystrophy|ARL6-related_disorder|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55": 1,
    "not_specified|Retinitis_pigmentosa|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|ARL6-related_disorder|not_provided": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Autosomal_recessive_retinitis_pigmentosa|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa|ARL6-related_disorder|Retinitis_pigmentosa_55|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_3|ARL6-related_disorder": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|not_provided|ARL6-related_disorder": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Retinitis_pigmentosa|not_specified": 1,
    "not_specified|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3": 1,
    "Cone-rod_dystrophy|Retinal_dystrophy|Optic_atrophy": 1,
    "Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|ARL6-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|not_provided|ARL6-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_1|_modifier_of": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_3|Inborn_genetic_diseases|ARL6-related_disorder": 1,
    "Retinitis_pigmentosa_55|not_provided|not_specified|Bardet-Biedl_syndrome_3|ARL6-related_disorder|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_3|Retinitis_pigmentosa_55|Bardet-Biedl_syndrome": 1,
    "not_provided|ARL6-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa_55|Bardet-Biedl_syndrome_3|not_provided|ARL6-related_disorder|Retinitis_pigmentosa": 1,
    "not_provided|Bardet-Biedl_syndrome|Retinitis_Pigmentosa|_Recessive": 1,
    "Restless_legs": 1,
    "Hereditary_coproporphyria|not_provided": 13,
    "not_provided|Hereditary_coproporphyria": 14,
    "CPOX-related_disorder": 6,
    "not_provided|Hereditary_coproporphyria|Coproporphyria": 1,
    "not_provided|Harderoporphyria": 1,
    "Coproporphyria": 7,
    "Harderoporphyria|Hereditary_coproporphyria|CPOX-related_hereditary_coproporphyria|not_provided": 1,
    "CPOX-related_disorder|not_provided": 2,
    "not_provided|Hereditary_coproporphyria|CPOX-related_disorder": 1,
    "Hereditary_coproporphyria|Coproporphyria": 1,
    "not_specified|not_provided|Hereditary_coproporphyria": 1,
    "Harderoporphyria": 1,
    "COPROPORPHYRIA|_DIGENIC": 1,
    "Acute_intermittent_porphyria|not_specified|not_provided|Hereditary_coproporphyria": 1,
    "Harderoporphyria|Hereditary_coproporphyria": 1,
    "CPOX-related_hereditary_coproporphyria": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_coproporphyria|CPOX-related_disorder": 1,
    "CPOX-related_disorder|Hereditary_coproporphyria": 1,
    "Hereditary_coproporphyria|CPOX-related_disorder|not_provided": 2,
    "not_provided|Hereditary_coproporphyria|CPOX-related_hereditary_coproporphyria": 1,
    "not_provided|CPOX-related_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_coproporphyria|not_provided": 1,
    "Hereditary_coproporphyria|Harderoporphyria|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_coproporphyria|CPOX-related_disorder": 1,
    "not_provided|CPOX-related_disorder|Coproporphyria": 1,
    "not_provided|Hereditary_coproporphyria|Harderoporphyria": 1,
    "DCBLD2-related_disorder": 2,
    "COL8A1-related_disorder": 6,
    "FILIP1L-related_disorder": 16,
    "not_specified|FILIP1L-related_disorder": 1,
    "FILIP1L-related_disorder|not_specified": 1,
    "CMSS1-related_disorder": 1,
    "Pontocerebellar_hypoplasia|_type_11": 15,
    "Pontocerebellar_hypoplasia|_type_11|not_specified|not_provided": 1,
    "not_provided|TBC1D23-related_disorder": 1,
    "TBC1D23-related_disorder": 10,
    "Pontocerebellar_hypoplasia|_type_11|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia|_type_11": 1,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia|_type_11": 1,
    "HP:0000750%3B_HP:0001263": 4,
    "Pontocerebellar_hypoplasia|_type_11|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia|_type_11|Pontoneocerebellar_hypoplasia": 3,
    "TOMM70-related_neurodevelopmental_disorder": 2,
    "not_provided|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 6,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 104,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57": 159,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|Inborn_genetic_diseases": 14,
    "not_provided|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57": 14,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 1,
    "TFG-related_disorder": 3,
    "TFG-related_disorder|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57": 3,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|not_provided": 2,
    "Hereditary_spastic_paraplegia_57|not_provided": 1,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_provided": 3,
    "not_specified|not_provided|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|Inborn_genetic_diseases|TFG-related_disorder": 1,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Inborn_genetic_diseases": 5,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 1,
    "Inborn_genetic_diseases|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|TFG-related_disorder|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57": 1,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 2,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|not_provided|not_specified": 1,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_specified|not_provided|TFG-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57": 1,
    "not_specified|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57": 4,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_specified|not_provided|TFG-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_provided|not_specified|TFG-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 2,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_specified|not_provided": 2,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Inborn_genetic_diseases": 1,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 1,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|not_provided|Amyotrophic_Lateral_Sclerosis_with_Sensory_Neuropathy|See_cases": 1,
    "Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|Inborn_genetic_diseases": 2,
    "Hereditary_motor_and_sensory_neuropathy|_Okinawa_type|Hereditary_spastic_paraplegia_57|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_57|Hereditary_motor_and_sensory_neuropathy|_Okinawa_type": 1,
    "IMPG2-related_disorder|not_provided": 5,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_56|IMPG2-related_disorder": 1,
    "Retinitis_pigmentosa_56": 13,
    "Vitelliform_macular_dystrophy_5|not_specified|Retinitis_pigmentosa_56|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "Vitelliform_macular_dystrophy_5|Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa|Bardet-Biedl_syndrome": 1,
    "Retinal_dystrophy|Vitelliform_macular_dystrophy_5": 3,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_56": 1,
    "Retinitis_pigmentosa|not_provided|Vitelliform_macular_dystrophy_2": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_56": 2,
    "Retinitis_pigmentosa_56|Vitelliform_macular_dystrophy_5|Inborn_genetic_diseases|not_provided|IMPG2-related_disorder": 1,
    "Retinitis_pigmentosa_56|not_provided|Retinal_dystrophy|Macular_dystrophy": 1,
    "not_provided|Vitelliform_macular_dystrophy_5|Retinitis_pigmentosa_56": 1,
    "not_provided|IMPG2-related_disorder": 5,
    "not_provided|Vitelliform_macular_dystrophy_2": 15,
    "Vitelliform_macular_dystrophy_5": 2,
    "not_provided|Retinitis_pigmentosa_56|Retinal_dystrophy": 1,
    "not_provided|Vitelliform_macular_dystrophy_5": 3,
    "not_specified|Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_56|Vitelliform_macular_dystrophy_5|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "IMPG2-related_disorder|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|IMPG2-related_disorder|Retinal_dystrophy": 2,
    "Vitelliform_macular_dystrophy_5|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_5|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_56": 1,
    "not_provided|Retinitis_pigmentosa_56|Vitelliform_macular_dystrophy_5": 2,
    "Retinitis_pigmentosa_56|Vitelliform_macular_dystrophy_5|not_provided": 1,
    "Vitelliform_macular_dystrophy_5|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_56": 1,
    "Retinitis_pigmentosa_56|Retinal_dystrophy": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_56": 1,
    "Retinitis_pigmentosa_56|Vitelliform_macular_dystrophy_5": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "IMPG2-related_disorder|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "Vitelliform_macular_dystrophy_5|Retinitis_pigmentosa_56|not_provided": 2,
    "Prostate_cancer|not_provided|Inborn_genetic_diseases": 1,
    "IMPG2-related_disorder|Retinitis_pigmentosa|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_56|Retinal_dystrophy|not_provided": 2,
    "IMPG2-related_disorder": 1,
    "Retinitis_pigmentosa_56|not_provided": 1,
    "Retinitis_pigmentosa_56|Vitelliform_macular_dystrophy_5|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_56": 1,
    "IMPG2-related_disorder|Inborn_genetic_diseases": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Macular_dystrophy": 1,
    "Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Vitelliform_macular_dystrophy_5": 1,
    "Vitelliform_macular_dystrophy_3": 3,
    "Vitelliform_macular_dystrophy_2": 21,
    "Retinitis_pigmentosa_56|not_provided|Retinal_dystrophy": 1,
    "IMPG2-related_disorder|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|Vitelliform_macular_dystrophy_5|Retinitis_pigmentosa_56|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Vitelliform_macular_dystrophy_5|not_provided": 1,
    "IMPG2-related_recessive_retinopathy|not_provided": 1,
    "Arthrogryposis_Multiplex_Congenita_and_Immunodeficiency": 1,
    "arthrogryposis_multiplex_congenita_with_neutropenia_and_early_respiratory_failure": 1,
    "SENP7-associated_disorder": 1,
    "not_provided|TRMT10C-related_disorder": 1,
    "TRMT10C-related_disorder": 3,
    "Mitochondrial_disease|Combined_oxidative_phosphorylation_defect_type_30|TRMT10C-related_disorder|See_cases|not_specified|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_30": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_30": 1,
    "Combined_oxidative_phosphorylation_defect_type_30|Mitochondrial_disease": 1,
    "ZBTB11-related_disorder": 8,
    "Intellectual_developmental_disorder|_autosomal_recessive_69": 17,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_69": 1,
    "not_provided|ZBTB11-related_disorder": 1,
    "NFKBIZ-related_disorder": 2,
    "CBLB-related_disorder": 13,
    "CBLB-related_disorder|not_specified": 1,
    "Autoimmune_disease|_multisystem|_infantile-onset|_3": 4,
    "CBLB-related_disorder|not_provided": 3,
    "CBLB-related_disorder|not_specified|not_provided": 1,
    "not_specified|CBLB-related_disorder": 1,
    "not_provided|CBLB-related_disorder": 1,
    "IFT57-related_disorder|not_provided": 2,
    "not_provided|IFT57-related_disorder": 4,
    "Orofaciodigital_syndrome_18": 4,
    "not_provided|Orofaciodigital_syndrome_18": 1,
    "NECTIN3-related_disorder": 11,
    "NECTIN3-related_disorder|not_provided": 2,
    "NECTIN3-related_disorder|Developmental_cataract": 1,
    "C_syndrome": 24,
    "C_syndrome|not_provided": 3,
    "CD96-related_disorder|not_specified": 1,
    "not_specified|CD96-related_disorder": 1,
    "not_provided|CD96-related_disorder": 1,
    "CD96-related_disorder|not_provided": 1,
    "CD96-related_disorder": 3,
    "not_specified|not_provided|CD96-related_disorder": 1,
    "not_provided|C_syndrome": 1,
    "Hypotrichosis_15": 4,
    "Monoclonal_B-Cell_Lymphocytosis": 10,
    "NEPRO-related_disorder": 8,
    "Abnormal_cerebral_white_matter_morphology|Microcephaly": 2,
    "not_provided|NEPRO-related_disorder": 2,
    "RMP64-related_condition|NEPRO-related_disorder": 1,
    "Anauxetic_dysplasia_3|not_provided": 2,
    "NEPRO-related_disorder|not_provided": 2,
    "Anauxetic_dysplasia_3": 2,
    "CFAP44-related_disorder": 10,
    "CFAP44-related_disorder|not_provided": 7,
    "Spermatogenic_failure_20": 11,
    "not_provided|CFAP44-related_disorder": 2,
    "CFAP44-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "CFAP44-related_disorder|Spermatogenic_failure_20": 1,
    "Marfanoid_habitus_and_intellectual_disability|not_specified": 4,
    "Cowden_syndrome|not_specified": 3,
    "NAA50-related_disorder": 2,
    "not_provided|NAA50-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_93": 27,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_93|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_93|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_cutis_laxa_type_2D": 4,
    "Developmental_and_epileptic_encephalopathy_93|not_provided": 1,
    "ATP6V1A-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy_93|Autosomal_recessive_cutis_laxa_type_2D": 1,
    "ATP6V1A-related_disorder|not_provided": 2,
    "not_provided|ATP6V1A-related_disorder": 6,
    "ATP6V1A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_2": 111,
    "not_provided|ATP6V1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_93": 1,
    "Encephalopathy|Developmental_and_epileptic_encephalopathy_93": 1,
    "Cerebral_visual_impairment_and_intellectual_disability|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_93": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_93": 1,
    "not_provided|Autosomal_recessive_cutis_laxa_type_2D": 1,
    "Autosomal_recessive_cutis_laxa_type_2D|Developmental_and_epileptic_encephalopathy_93|not_provided": 1,
    "Vascular_disorder|not_provided|ATP6V1A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_93|Autosomal_recessive_cutis_laxa_type_2D|not_provided": 1,
    "Hereditary_essential_tremor": 10,
    "DRD3-related_disorder": 2,
    "not_provided|Tremor|_hereditary_essential|_1": 2,
    "Tremor|_hereditary_essential|_1|not_provided": 4,
    "Tremor|_hereditary_essential|_1|DRD3-related_disorder": 1,
    "not_specified|Tremor|_hereditary_essential|_1": 1,
    "Tremor|_hereditary_essential|_1": 4,
    "not_provided|not_specified|DRD3-related_disorder": 1,
    "Tremor|_hereditary_essential|_1|DRD3-related_disorder|not_provided": 1,
    "Schizophrenia|_susceptibility_to|not_specified|Essential_tremor|_susceptibility_to|Tremor|_hereditary_essential|_1|not_provided|DRD3-related_disorder": 1,
    "ZBTB20-related_disorder|Primrose_syndrome|not_provided": 1,
    "ZBTB20-related_disorder": 9,
    "Primrose_syndrome|not_provided": 5,
    "not_provided|ZBTB20-related_disorder|Inborn_genetic_diseases|Primrose_syndrome": 1,
    "not_provided|ZBTB20-related_disorder|not_specified": 1,
    "Primrose_syndrome": 50,
    "Clinodactyly_of_the_4th_toe|Moderate_global_developmental_delay|Abnormal_facial_shape|Clinodactyly_of_the_5th_finger|Autistic_behavior": 1,
    "ZBTB20-related_disorder|not_provided": 9,
    "Intellectual_disability|not_provided|Primrose_syndrome": 1,
    "not_provided|ZBTB20-related_disorder": 3,
    "Inborn_genetic_diseases|Primrose_syndrome|See_cases|not_provided": 1,
    "Primrose_syndrome|Marfanoid_habitus_and_intellectual_disability": 1,
    "Intellectual_disability|Primrose_syndrome": 3,
    "Primrose_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Primrose_syndrome": 3,
    "SHORT_syndrome|not_provided|Primrose_syndrome": 1,
    "ZBTB20-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Primrose_syndrome|not_specified|not_provided": 1,
    "ZBTB20-related_disorder|Inborn_genetic_diseases|Primrose_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|ZBTB20-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Primrose_syndrome|not_provided": 1,
    "not_specified|not_provided|ZBTB20-related_disorder": 1,
    "Adams-Oliver_syndrome": 8,
    "Adams-Oliver_syndrome_1|not_provided": 17,
    "ARHGAP31-related_disorder": 25,
    "ARHGAP31-related_disorder|not_provided": 11,
    "not_provided|ARHGAP31-related_disorder": 8,
    "not_provided|Adams-Oliver_syndrome": 1,
    "not_specified|not_provided|Adams-Oliver_syndrome_1": 3,
    "Adams-Oliver_syndrome_1": 24,
    "Inborn_genetic_diseases|ARHGAP31-related_disorder": 1,
    "not_provided|Adams-Oliver_syndrome_1": 8,
    "Inborn_genetic_diseases|Adams-Oliver_syndrome_1": 2,
    "Adams-Oliver_syndrome_1|ARHGAP31-related_disorder|not_provided|not_specified": 1,
    "Adams-Oliver_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "ARHGAP31-related_disorder|not_specified|not_provided|Adams-Oliver_syndrome_1": 1,
    "not_specified|ARHGAP31-related_disorder": 1,
    "not_specified|ARHGAP31-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Adams-Oliver_syndrome_1|not_provided|not_specified": 2,
    "Adams-Oliver_syndrome_1|not_specified|not_provided": 2,
    "ARHGAP31-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Adams-Oliver_syndrome_1|ARHGAP31-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|ARHGAP31-related_disorder|not_specified": 1,
    "Adams-Oliver_syndrome_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Adams-Oliver_syndrome_1|ARHGAP31-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|ARHGAP31-related_disorder": 1,
    "not_specified|not_provided|ARHGAP31-related_disorder": 1,
    "Inborn_genetic_diseases|ARHGAP31-related_disorder|not_provided": 2,
    "Adams-Oliver_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Adams-Oliver_syndrome": 1,
    "Adams-Oliver_syndrome_1|Inborn_genetic_diseases": 1,
    "ARHGAP31-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Dowling-Degos_disease_4|not_provided": 3,
    "not_provided|POGLUT1-related_disorder": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2R1": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2R1|not_provided|Dowling-Degos_disease_4": 1,
    "not_provided|Dowling-Degos_disease_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2R1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2R1|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2R1": 2,
    "Inborn_genetic_diseases|Dowling-Degos_disease_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2R1|not_provided": 1,
    "Dowling-Degos_disease_4": 2,
    "POGLUT1-related_disorder|not_provided": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_31": 8,
    "TIMMDC1-related_disorder": 2,
    "TIMMDC1-related_disorder|not_provided": 7,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_31": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_31|See_cases": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_31": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_31|not_provided": 2,
    "CFAP91-related_condition|Spermatogenic_failure_51|Male_infertility_with_teratozoospermia_due_to_single_gene_mutation": 1,
    "Spermatogenic_failure_51|Male_infertility_with_teratozoospermia_due_to_single_gene_mutation": 1,
    "CFAP91-related_condition": 1,
    "Spermatogenic_failure_51": 1,
    "Hearing_loss|_autosomal_recessive_121": 1,
    "Hearing_loss|_autosomal_recessive|Hearing_loss|_autosomal_recessive_121": 2,
    "GPR156-related_disorder": 3,
    "Alkaptonuria": 535,
    "not_provided|Alkaptonuria": 15,
    "Alkaptonuria|not_provided": 6,
    "Alkaptonuria|Inborn_genetic_diseases": 5,
    "Alkaptonuria|not_provided|HGD-related_disorder": 1,
    "HGD-related_disorder": 1,
    "Alkaptonuria|HGD-related_disorder": 6,
    "See_cases|Alkaptonuria|not_provided": 1,
    "Inborn_genetic_diseases|Alkaptonuria": 8,
    "not_specified|Alkaptonuria": 5,
    "Alkaptonuria|not_specified": 3,
    "HGD-related_disorder|not_provided|Alkaptonuria": 2,
    "Alkaptonuria|not_specified|not_provided": 1,
    "See_cases|Alkaptonuria": 1,
    "RABL3-related_disorder": 14,
    "not_provided|RABL3-related_disorder": 2,
    "Pancreatic_cancer|_susceptibility_to|_5": 1,
    "STXBP5L-related_disorder": 10,
    "not_provided|STXBP5L-related_disorder": 1,
    "not_specified|STXBP5L-related_disorder": 1,
    "not_specified|POLQ-related_disorder": 13,
    "POLQ-related_disorder": 28,
    "not_provided|POLQ-related_disorder": 7,
    "POLQ-related_disorder|not_specified": 13,
    "POLQ-related_disorder|not_provided": 8,
    "not_specified|POLQ-related_disorder|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|POLQ-related_disorder": 1,
    "not_provided|not_specified|POLQ-related_disorder": 1,
    "not_specified|not_provided|POLQ-related_disorder": 1,
    "not_provided|POLQ-related_disorder|not_specified": 2,
    "POLQ-related_disorder|not_specified|not_provided": 1,
    "Senior-Loken_syndrome_5": 99,
    "Senior-Loken_syndrome_5|not_provided": 1,
    "IQCB1-related_disorder|Nephronophthisis": 4,
    "Nephronophthisis|Senior-Loken_syndrome_5": 34,
    "not_provided|Senior-Loken_syndrome_5|Nephronophthisis": 2,
    "not_provided|IQCB1-related_disorder|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_5|Nephronophthisis": 3,
    "Senior-Loken_syndrome_5|Nephronophthisis": 25,
    "not_provided|Nephronophthisis|not_specified": 2,
    "IQCB1-related_disorder|Retinal_dystrophy|Senior-Loken_syndrome_5|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|not_provided|not_specified|Senior-Loken_syndrome_5|IQCB1-related_disorder": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_5": 2,
    "IQCB1-related_disorder|Nephronophthisis|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Senior-Loken_syndrome_5": 1,
    "Nephronophthisis|not_provided|Senior-Loken_syndrome_5": 2,
    "Senior-Loken_syndrome_5|Nephronophthisis|Inborn_genetic_diseases": 2,
    "Senior-Loken_syndrome_5|Retinal_dystrophy|Nephronophthisis": 2,
    "Nephronophthisis|Inborn_genetic_diseases|Senior-Loken_syndrome_5": 4,
    "Nephronophthisis|Retinal_dystrophy|not_provided|Senior-Loken_syndrome_5": 1,
    "not_provided|not_specified|Nephronophthisis|Senior-Loken_syndrome_5|Inborn_genetic_diseases": 1,
    "IQCB1-related_disorder|Nephronophthisis|not_provided|Retinitis_pigmentosa|Senior-Loken_syndrome_5": 1,
    "Senior-Loken_syndrome_5|not_provided|Nephronophthisis": 3,
    "IQCB1-related_disorder": 1,
    "not_provided|Senior-Loken_syndrome_5": 5,
    "Senior-Loken_syndrome_5|Nephronophthisis|Retinal_dystrophy|Renal_dysplasia_and_retinal_aplasia|not_provided|Inborn_genetic_diseases|IQCB1-related_disorder": 1,
    "Senior-Loken_syndrome_5|Inborn_genetic_diseases|Nephronophthisis": 5,
    "Senior-Loken_syndrome_5|Retinal_dystrophy|Nephronophthisis|Renal_dysplasia_and_retinal_aplasia": 1,
    "Nephronophthisis|Renal_dysplasia_and_retinal_aplasia": 2,
    "Nephronophthisis|IQCB1-related_disorder": 2,
    "Nephronophthisis|Leber_congenital_amaurosis|Senior-Loken_syndrome_5": 1,
    "not_specified|Nephronophthisis|not_provided|Senior-Loken_syndrome_5": 2,
    "not_specified|Senior-Loken_syndrome_5|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|IQCB1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Senior-Loken_syndrome_5": 1,
    "Nephronophthisis|Senior-Loken_syndrome_5|not_provided": 1,
    "Nephronophthisis|Senior-Loken_syndrome_5|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Nephronophthisis|not_provided|Senior-Loken_syndrome_5": 1,
    "Senior-Loken_syndrome_5|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|Senior-Loken_syndrome_5|IQCB1-related_disorder": 1,
    "Senior-Loken_syndrome_5|IQCB1-related_disorder|Nephronophthisis|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|IQCB1-related_disorder|Senior-Loken_syndrome_5": 2,
    "not_provided|Senior-Loken_syndrome_5|not_specified|Nephronophthisis": 1,
    "not_specified|not_provided|Senior-Loken_syndrome_5|Nephronophthisis": 2,
    "Nephronophthisis|Senior-Loken_syndrome_5|Inborn_genetic_diseases": 1,
    "Nephronophthisis|IQCB1-related_disorder|Senior-Loken_syndrome_5|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Senior-Loken_syndrome_5": 1,
    "not_provided|Nephronophthisis|Senior-Loken_syndrome_5": 1,
    "not_provided|Nephronophthisis|Leber_congenital_amaurosis|Senior-Loken_syndrome_5": 1,
    "Nephronophthisis|See_cases": 1,
    "ILDR1-related_disorder|not_provided|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_42|not_provided|not_specified": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_42": 16,
    "ILDR1-related_disorder": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_42|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_42": 6,
    "not_specified|not_provided|ILDR1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_42|Inborn_genetic_diseases|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "ILDR1-related_disorder|not_specified": 2,
    "not_provided|ILDR1-related_disorder|Childhood_onset_hearing_loss": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_42|not_specified|not_provided|Hearing_impairment": 1,
    "Congenital_sensorineural_hearing_impairment|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_42|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_42": 1,
    "not_provided|not_specified|Hearing_impairment|Inborn_genetic_diseases": 1,
    "ILDR1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_42|Hearing_loss|_autosomal_recessive": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 569,
    "Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia|Hypocalcemia|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism": 4,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|Autosomal_dominant_hypocalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 2,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Nephrolithiasis/nephrocalcinosis": 512,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 485,
    "Familial_hypocalciuric_hypercalcemia_1|Hereditary_cancer-predisposing_syndrome|not_specified|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 228,
    "Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 129,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|not_specified|Nephrolithiasis/nephrocalcinosis|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|not_specified|not_provided|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis": 162,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 2,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|not_provided|not_specified|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 8,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 2,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided": 4,
    "CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|not_provided|Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified|not_provided": 1,
    "CASR-related_disorder": 15,
    "CASR-related_calcium_metabolism_disorders|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|not_provided|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 2,
    "Familial_hypoparathyroidism|not_specified|not_provided|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|CASR-related_disorder": 2,
    "Bartter_syndrome_with_hypocalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia": 20,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified": 5,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 4,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 6,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 18,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Neonatal_severe_primary_hyperparathyroidism": 1,
    "not_specified|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1": 26,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 2,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 4,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 2,
    "not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis": 4,
    "Autosomal_dominant_hypocalcemia_1": 15,
    "not_provided|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 3,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 119,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1": 1,
    "not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified": 1,
    "not_provided|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 2,
    "Neonatal_severe_primary_hyperparathyroidism": 5,
    "not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 20,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 2,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided": 7,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Bartter_syndrome_with_hypocalcemia": 1,
    "CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_specified|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 12,
    "Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|Nephrolithiasis/nephrocalcinosis": 1,
    "Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis": 6,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1": 1,
    "CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 2,
    "not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 21,
    "Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided": 14,
    "not_provided|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 3,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 2,
    "not_specified|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 3,
    "Autosomal_dominant_hypocalcemia_1|Bartter_syndrome_with_hypocalcemia|Familial_hypocalciuric_hypercalcemia|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 2,
    "not_provided|Familial_hypocalciuric_hypercalcemia": 2,
    "Autosomal_dominant_hypocalcemia_1|CASR-related_disorder": 1,
    "Nephrolithiasis/nephrocalcinosis|Bartter_syndrome_with_hypocalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "CASR-related_disorder|Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided|CASR-related_disorder|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided": 2,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 5,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Nephrolithiasis/nephrocalcinosis": 4,
    "not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 6,
    "Familial_hypocalciuric_hypercalcemia|not_provided": 2,
    "Familial_hypocalciuric_hypercalcemia_1|not_provided": 2,
    "Nephrolithiasis/nephrocalcinosis|not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 4,
    "Neonatal_severe_primary_hyperparathyroidism|not_specified|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 3,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Bartter_syndrome_with_hypocalcemia|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1": 2,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Familial_hypocalciuric_hypercalcemia_1": 2,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 12,
    "Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_specified|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 5,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|not_provided": 4,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified": 2,
    "Hypercalcemia|not_specified|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_specified|not_provided|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|Nephrolithiasis/nephrocalcinosis|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|not_provided": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 1,
    "not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia": 1,
    "Autosomal_dominant_hypocalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 1,
    "not_provided|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|CASR-related_disorder|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|CASR-related_disorder|Neonatal_severe_primary_hyperparathyroidism|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 2,
    "CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 4,
    "Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 3,
    "not_provided|not_specified|CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_hypoparathyroidism": 1,
    "CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Nephrolithiasis/nephrocalcinosis|not_specified|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 2,
    "Hypocalcemia|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|not_specified|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_specified|Familial_hypocalciuric_hypercalcemia_1|not_provided|See_cases|CASR-related_disorder|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 3,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia|not_provided|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_specified": 5,
    "not_specified|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_specified|not_provided|CASR-related_disorder": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Hereditary_cancer-predisposing_syndrome|CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism": 1,
    "not_specified|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 6,
    "not_specified|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism": 2,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 2,
    "Hypercalcemia|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 5,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 9,
    "Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia": 1,
    "not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|CASR-related_disorder": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 2,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|not_specified|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|CASR-related_disorder": 1,
    "Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided|Familial_hypocalciuric_hypercalcemia": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified": 2,
    "Nephrolithiasis/nephrocalcinosis|CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Hereditary_cancer-predisposing_syndrome|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Hypercalcemia|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 1,
    "not_provided|not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided|CASR-related_disorder": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|not_specified|not_provided": 1,
    "CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 2,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism": 4,
    "Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|not_specified|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|not_provided": 1,
    "Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Nephrolithiasis/nephrocalcinosis|not_specified": 2,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|not_specified|Familial_hypocalciuric_hypercalcemia": 1,
    "not_specified|CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 2,
    "not_specified|Nephrolithiasis/nephrocalcinosis": 3,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_specified": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 2,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|not_specified": 1,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified": 1,
    "not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_provided|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis": 2,
    "Hypocalcemia|CASR-related_disorder": 1,
    "CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 2,
    "Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_specified": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided|Familial_hypocalciuric_hypercalcemia": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "CASR-related_disorder|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism": 1,
    "not_specified|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|not_specified": 1,
    "Nephrolithiasis/nephrocalcinosis|CASR-related_disorder": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 2,
    "CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|not_specified|not_provided": 1,
    "not_specified|CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Nephrolithiasis/nephrocalcinosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|CASR-related_disorder|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|CASR-related_disorder|Nephrolithiasis/nephrocalcinosis": 2,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Nephrolithiasis/nephrocalcinosis|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_specified": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis": 2,
    "not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism": 2,
    "Familial_hypoparathyroidism": 33,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Autosomal_dominant_hypocalcemia": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|CASR-related_disorder": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 1,
    "Idiopathic_generalized_epilepsy|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis|Familial_hypoparathyroidism|not_specified": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|not_specified|not_provided": 1,
    "CASR-related_disorder|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|not_provided|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_specified|not_provided": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism": 1,
    "not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Bartter_syndrome_with_hypocalcemia": 1,
    "CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "not_specified|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 3,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_specified": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|CASR-related_disorder": 1,
    "not_provided|Nephrolithiasis/nephrocalcinosis": 5,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Nephrolithiasis/nephrocalcinosis": 2,
    "not_specified|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 2,
    "not_specified|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_provided|Primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|CASR-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_hypocalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 2,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Parathyroid_gland_adenoma|Hypercalcemia|Hypocalciuria|Hypertrophic_cardiomyopathy|not_provided|Familial_hypocalciuric_hypercalcemia": 1,
    "CASR-related_disorder|Autosomal_dominant_hypocalcemia_1|not_provided": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Bartter_syndrome_with_hypocalcemia|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_provided": 1,
    "Autosomal_dominant_hypocalcemia_1|Bartter_syndrome_with_hypocalcemia": 1,
    "not_provided|Hypercalcemia": 1,
    "not_specified|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia|Hereditary_cancer-predisposing_syndrome|Nephrolithiasis/nephrocalcinosis": 1,
    "Hypercalcaemia|_hypocalciuric": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|not_specified|not_provided|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism": 1,
    "Nephrolithiasis/nephrocalcinosis|not_specified|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia": 2,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis": 2,
    "Bartter_syndrome|Familial_hypokalemia-hypomagnesemia": 6,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|Nephrolithiasis/nephrocalcinosis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_specified": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|not_provided|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|CASR-related_disorder": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|CASR-related_disorder|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia|not_specified": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Hereditary_cancer-predisposing_syndrome|not_specified|Nephrolithiasis/nephrocalcinosis|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism": 1,
    "CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|not_specified|Familial_hypocalciuric_hypercalcemia": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_provided|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1": 1,
    "not_provided|CASR-related_disorder|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8": 1,
    "Serum_calcium_level|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism|Malignant_tumor_of_breast|not_specified|not_provided|Neonatal_severe_primary_hyperparathyroidism|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1": 1,
    "not_provided|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia_1|not_specified|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Bartter_disease_type_3|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia_1": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Familial_hypocalciuric_hypercalcemia": 1,
    "not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Nephrolithiasis/nephrocalcinosis": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Nephrolithiasis/nephrocalcinosis": 1,
    "Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|not_specified|Familial_hypocalciuric_hypercalcemia_1|not_provided": 1,
    "Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypoparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|not_specified|Nephrolithiasis/nephrocalcinosis": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Neonatal_severe_primary_hyperparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Prostate_cancer|Nephrolithiasis/nephrocalcinosis": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Autosomal_dominant_hypocalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia_1|CASR-related_disorder|Nephrolithiasis/nephrocalcinosis|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia": 1,
    "Nephrolithiasis/nephrocalcinosis|Autosomal_dominant_hypocalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia": 1,
    "Familial_hypocalciuric_hypercalcemia|Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia_1|Epilepsy|_idiopathic_generalized|_susceptibility_to|_8|Hereditary_cancer-predisposing_syndrome": 1,
    "Autosomal_dominant_hypocalcemia_1|Nephrolithiasis/nephrocalcinosis|not_provided|Neonatal_severe_primary_hyperparathyroidism|Familial_hypocalciuric_hypercalcemia|Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|not_provided|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1": 4,
    "Familial_hypocalciuric_hypercalcemia_1|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Autosomal_dominant_hypocalcemia_1": 8,
    "Familial_hypocalciuric_hypercalcemia|Familial_hypoparathyroidism|Neonatal_severe_primary_hyperparathyroidism|Hypocalcemia": 1,
    "Autosomal_dominant_hypocalcemia_1|Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|not_provided|Familial_hypoparathyroidism": 1,
    "Familial_hypocalciuric_hypercalcemia_1|Neonatal_severe_primary_hyperparathyroidism|not_provided|Autosomal_dominant_hypocalcemia_1|Familial_hypoparathyroidism": 1,
    "Peeling_skin_syndrome_4|not_provided": 1,
    "Peeling_skin_syndrome_4": 3,
    "not_provided|Peeling_skin_syndrome_4": 1,
    "CSTA-related_disorder": 2,
    "Ovarian_cancer|not_specified": 4,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 3,
    "ADCY5-related_disorder|not_provided": 6,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia": 3,
    "not_provided|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 1,
    "not_provided|ADCY5-related_disorder": 6,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Inborn_genetic_diseases": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 36,
    "not_specified|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided": 3,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia": 3,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia": 4,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided": 2,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_specified|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided": 3,
    "Inborn_genetic_diseases|Dyskinesia_with_orofacial_involvement|_autosomal_recessive": 1,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Dyskinesia_with_orofacial_involvement|_autosomal_recessive": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_specified|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia": 1,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|ADCY5-related_disorder": 1,
    "not_specified|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 3,
    "ADCY5-related_disorder": 4,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 6,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Inborn_genetic_diseases|ADCY5-related_disorder|not_provided": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided": 3,
    "not_provided|Morphological_central_nervous_system_abnormality": 1,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 3,
    "Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 1,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided|not_specified": 1,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_recessive": 2,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_specified": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_specified|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 10,
    "not_provided|ADCY5-related_disorder|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 1,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|See_cases|Neurodevelopmental_delay": 1,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Dyskinesia_with_orofacial_involvement|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 1,
    "ADCY5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|not_specified|not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant": 1,
    "not_provided|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_recessive": 1,
    "Language_disorder|Parkinsonian_disorder|Dysarthria": 1,
    "not_provided|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia": 2,
    "Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_provided": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|not_specified|not_provided": 1,
    "Dyskinesia_with_orofacial_involvement|_autosomal_dominant|Dyskinesia_with_orofacial_involvement|_autosomal_recessive|Neurodevelopmental_disorder_with_hyperkinetic_movements_and_dyskinesia|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided": 32,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 12,
    "Aortic_aneurysm|_familial_thoracic_7": 927,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 11,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 171,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 117,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 5,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 27,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 2,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7": 38,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7": 20,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_7|not_provided": 2,
    "Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 4,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified": 3,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided": 5,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 2,
    "Aortic_aneurysm|_familial_thoracic_7|Connective_tissue_disorder": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7": 2,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Connective_tissue_disorder|MYLK-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_7": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified|Connective_tissue_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified": 20,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_specified": 11,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided": 26,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_specified": 6,
    "not_specified|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 23,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7": 3,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 37,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7": 15,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Connective_tissue_disorder|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided": 5,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 19,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder": 2,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 3,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 6,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified": 4,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 4,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Aortic_aneurysm|_familial_abdominal|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Disproportionate_tall_stature|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|not_provided": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "MYLK-related_disorder": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_7": 8,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified|MYLK-related_disorder": 1,
    "Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided": 7,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_7": 2,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|not_provided": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided": 7,
    "MYLK-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 3,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 4,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7": 3,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7": 4,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 4,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_7|Connective_tissue_disorder|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7|Cardiovascular_phenotype": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|MYLK-related_disorder": 1,
    "not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "MYLK-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_7": 2,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Visceral_myopathy_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Connective_tissue_disorder|not_provided|MYLK-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Visceral_myopathy_1|Megacystis|_microcolon|_hypoperistalsis_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified|not_provided": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 2,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYLK-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|MYLK-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Atrial_septal_defect|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_specified": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Megacystis|_microcolon|_hypoperistalsis_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_7": 1,
    "MYLK-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified|Megacystis|_microcolon|_hypoperistalsis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_7|not_provided|Connective_tissue_disorder|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|MYLK-related_disorder": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_aortic_aneurysms|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 2,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|MYLK-related_disorder": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided|MYLK-related_disorder": 1,
    "not_provided|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 2,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided": 2,
    "not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 3,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_specified|not_provided": 3,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Disproportionate_tall_stature|not_provided": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Marfan_syndrome|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7|not_specified": 1,
    "Connective_tissue_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_specified": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7|not_specified": 1,
    "not_specified|MYLK-related_disorder|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Congenital_aneurysm_of_ascending_aorta|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|MYLK-related_disorder": 1,
    "not_provided|Megacystis|_microcolon|_hypoperistalsis_syndrome|Aortic_aneurysm|_familial_thoracic_7|not_specified": 1,
    "MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis|_microcolon|_hypoperistalsis_syndrome|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|not_provided": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided|MYLK-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|MYLK-related_disorder|not_specified|Aortic_aneurysm|_familial_thoracic_7|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|not_specified|not_provided": 1,
    "not_provided|Megacystis|_microcolon|_hypoperistalsis_syndrome|Aortic_aneurysm|_familial_thoracic_7|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Aortic_aneurysm|_familial_thoracic_7|Connective_tissue_disorder|MYLK-related_disorder|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-Microcolon_Hypoperistalsis_Syndrome_1": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "not_specified|Megacystis|_microcolon|_hypoperistalsis_syndrome|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|not_provided": 2,
    "Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_specified|Connective_tissue_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_7|not_provided|not_specified|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_7|MYLK-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_7|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Aortic_aneurysm|_familial_thoracic_7|See_cases": 1,
    "MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis|_microcolon|_hypoperistalsis_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "not_specified|MYLK-related_disorder|not_provided|Congenital_aneurysm_of_ascending_aorta|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_7": 1,
    "MYLK-related_disorder|Aortic_aneurysm|_familial_thoracic_7|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_1": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_7": 1,
    "Coronary_heart_disease|_susceptibility_to|_5|KALRN-related_disorder": 1,
    "KALRN-related_disorder": 36,
    "KALRN-related_disorder|not_provided": 2,
    "Coronary_heart_disease|_susceptibility_to|_5": 1,
    "not_provided|KALRN-related_disorder": 2,
    "not_provided|Oroticaciduria": 15,
    "Oroticaciduria": 152,
    "not_provided|Hereditary_orotic_aciduria|_type_1": 2,
    "not_provided|Hereditary_orotic_aciduria|_type_1|Oroticaciduria": 3,
    "Hereditary_orotic_aciduria|_type_1": 32,
    "Hereditary_orotic_aciduria|_type_1|Oroticaciduria|not_specified|not_provided": 1,
    "not_provided|Hereditary_orotic_aciduria|_type_1|UMPS-related_disorder": 1,
    "UMPS-related_disorder": 3,
    "Cardiomyopathy|Oroticaciduria": 1,
    "Hereditary_orotic_aciduria|Hereditary_orotic_aciduria|_type_1": 1,
    "Inborn_genetic_diseases|Hereditary_orotic_aciduria|_type_1": 2,
    "Hereditary_orotic_aciduria|_type_1|Inborn_genetic_diseases": 4,
    "Hereditary_orotic_aciduria": 2,
    "Oroticaciduria|Hereditary_orotic_aciduria|_type_1|UMPS-related_disorder": 1,
    "not_specified|Hereditary_orotic_aciduria|_type_1": 1,
    "Hereditary_orotic_aciduria|_type_1|not_specified|not_provided|Oroticaciduria": 2,
    "UMPS-related_disorder|Hereditary_orotic_aciduria|_type_1": 1,
    "Hereditary_orotic_aciduria|_type_1|Inborn_genetic_diseases|Oroticaciduria": 1,
    "Inborn_genetic_diseases|Oroticaciduria|Hereditary_orotic_aciduria|_type_1": 1,
    "Hereditary_orotic_aciduria|not_provided|Hereditary_orotic_aciduria|_type_1|Oroticaciduria": 1,
    "Inborn_genetic_diseases|Oroticaciduria": 1,
    "Hereditary_orotic_aciduria|_type_1|not_provided|Oroticaciduria": 1,
    "Hereditary_orotic_aciduria|Hereditary_orotic_aciduria|_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_orotic_aciduria|_type_1|Oroticaciduria": 1,
    "Oroticaciduria|Hereditary_orotic_aciduria|_type_1": 3,
    "Hereditary_orotic_aciduria|_type_1|Oroticaciduria": 1,
    "not_provided|Oroticaciduria|Hereditary_orotic_aciduria|_type_1": 2,
    "Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies|not_provided": 1,
    "Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies": 25,
    "ZNF148-related_disorder": 6,
    "Inborn_genetic_diseases|ZNF148-related_disorder": 1,
    "not_provided|Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies": 2,
    "Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies|Intellectual_disability": 1,
    "Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "not_provided|ZNF148-related_disorder": 1,
    "ZNF148-related_disorder|Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies": 1,
    "ZNF148-related_disorder|Global_developmental_delay|_absent_or_hypoplastic_corpus_callosum|_and_dysmorphic_facies|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|UROC1-related_disorder": 3,
    "not_provided|Urocanate_hydratase_deficiency|not_specified": 1,
    "UROC1-related_disorder": 6,
    "not_provided|Urocanate_hydratase_deficiency": 3,
    "not_provided|UROC1-related_disorder|not_specified": 1,
    "Urocanate_hydratase_deficiency": 7,
    "UROC1-related_disorder|not_provided": 1,
    "Urocanate_hydratase_deficiency|not_provided": 4,
    "Urocanate_hydratase_deficiency|not_specified": 1,
    "not_specified|not_provided|Urocanate_hydratase_deficiency": 1,
    "PLXNA1-related_disorder|Dworschak-Punetha_neurodevelopmental_syndrome": 3,
    "PLXNA1-related_disorder|not_provided": 58,
    "not_provided|PLXNA1-related_disorder": 52,
    "not_specified|PLXNA1-related_disorder": 47,
    "not_provided|not_specified|PLXNA1-related_disorder": 2,
    "PLXNA1-related_disorder": 438,
    "PLXNA1-related_disorder|not_specified": 36,
    "HP:0000750%3B_HP:0001263%3B_HP:0001513": 1,
    "not_specified|not_provided|PLXNA1-related_disorder": 2,
    "Dworschak-Punetha_neurodevelopmental_syndrome|Neurodevelopmental_disorder": 3,
    "PLXNA1-associated_encephalopathy": 1,
    "not_specified|Dworschak-Punetha_neurodevelopmental_syndrome|PLXNA1-related_disorder": 1,
    "not_specified|Dworschak-Punetha_neurodevelopmental_syndrome": 2,
    "Dworschak-Punetha_neurodevelopmental_syndrome": 13,
    "not_specified|PLXNA1-related_disorder|PLXNA1-related_neurodevelopmental_disorder|Dworschak-Punetha_neurodevelopmental_syndrome": 1,
    "Neurodevelopmental_disorder|PLXNA1-related_disorder|Dworschak-Punetha_neurodevelopmental_syndrome": 1,
    "PLXNA1-related_disorder|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_variable_cerebral_and_eye_anomalies": 1,
    "PLXNA1-related_disorder|not_provided|not_specified": 1,
    "Dworschak-Punetha_neurodevelopmental_syndrome|Neurodevelopmental_disorder|not_specified": 1,
    "PLXNA1-related_disorder|PLXNA1-related_Neurodevelopmental_disorder_with_variable_cerebral_and_eye_anomalies": 1,
    "PLXNA1-related_disorder|Parkinson_disease|Parkinsonian_disorder|Vascular_parkinsonism|not_provided|not_specified": 1,
    "PLXNA1-related_disorder|Dworschak-Punetha_neurodevelopmental_syndrome|not_specified": 1,
    "Neurodevelopmental_disorder|PLXNA1-related_disorder": 1,
    "Dworschak-Punetha_neurodevelopmental_syndrome|not_specified": 1,
    "PLXNA1-related_disorder|Neurodevelopmental_disorder": 2,
    "not_provided|PLXNA1-related_disorder|not_specified": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_70|not_provided": 1,
    "MCM2-related_disorder|not_provided": 15,
    "Autosomal_dominant_nonsyndromic_hearing_loss_70": 7,
    "not_provided|MCM2-related_disorder": 8,
    "MCM2-related_disorder": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_70|MCM2-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_70|not_specified|not_provided": 1,
    "not_specified|MCM2-related_disorder": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_70": 2,
    "not_specified|not_provided|MCM2-related_disorder": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_70|not_provided": 1,
    "not_provided|MCM2-related_disorder|not_specified": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_70": 1,
    "not_specified|MCM2-related_disorder|not_provided": 1,
    "MCM2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_70": 1,
    "MGLL-related_disorder": 7,
    "not_provided|MGLL-related_disorder": 3,
    "SEC61A1-related_disorder|not_provided": 4,
    "Hyperuricemic_nephropathy|_familial_juvenile_type_4": 8,
    "Immunodeficiency|_common_variable|_15|Decreased_circulating_immunoglobulin_concentration": 1,
    "Neutropenia|_severe_congenital|_11|_autosomal_dominant": 1,
    "Hyperuricemic_nephropathy|_familial_juvenile_type_4|Inborn_genetic_diseases": 1,
    "not_provided|Hyperuricemic_nephropathy|_familial_juvenile_type_4": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided": 7,
    "Hyperuricemic_nephropathy|_familial_juvenile_type_4|not_specified|not_provided": 1,
    "SEC61A1-related_disorder": 2,
    "Inborn_genetic_diseases|Hyperuricemic_nephropathy|_familial_juvenile_type_4|Immunodeficiency|_common_variable|_15|Neutropenia|_severe_congenital|_11|_autosomal_dominant": 1,
    "Hyperuricemic_nephropathy|_familial_juvenile_type_4|Immunodeficiency|_common_variable|_15|Neutropenia|_severe_congenital|_11|_autosomal_dominant": 1,
    "Immunodeficiency|_common_variable|_15": 1,
    "not_provided|SEC61A1-related_disorder": 2,
    "Inborn_genetic_diseases|SEC61A1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_abnormalities": 2,
    "not_specified|Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_abnormalities": 1,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_abnormalities|not_specified": 1,
    "Autosomal_recessive_non-syndromic_intellectual_disability": 5,
    "Neurodevelopmental_disorder_with_progressive_spasticity_and_brain_abnormalities|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 543,
    "Deafness-lymphedema-leukemia_syndrome": 49,
    "not_provided|Deafness-lymphedema-leukemia_syndrome": 2,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided": 24,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 10,
    "Deafness-lymphedema-leukemia_syndrome|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases": 89,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 113,
    "Hereditary_cancer-predisposing_syndrome|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 166,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|not_provided": 5,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases": 31,
    "not_specified|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 3,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|Acute_myeloid_leukemia": 1,
    "not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 45,
    "not_provided|Acute_myeloid_leukemia|GATA2_deficiency_with_susceptibility_to_MDS/AML|Inborn_genetic_diseases|not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Inborn_genetic_diseases|not_provided|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 4,
    "not_provided|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 6,
    "not_specified|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Acute_myeloid_leukemia|GATA2-related_disorder|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases": 4,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided|Inborn_genetic_diseases": 5,
    "Acute_myeloid_leukemia|Myelodysplastic_syndrome|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer|Inborn_genetic_diseases|not_provided": 1,
    "GATA2-related_disorder|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome": 100,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 4,
    "Acute_myeloid_leukemia|not_provided": 12,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections": 1,
    "Acute_myeloid_leukemia|not_provided|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "not_provided|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Myelodysplastic_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|GATA2-related_disorder|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified|Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 3,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections": 2,
    "not_provided|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 2,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Acute_myeloid_leukemia": 4,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|not_specified": 2,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia": 3,
    "not_provided|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 5,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia": 148,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 12,
    "GATA2-related_disorder": 5,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2_deficiency_with_susceptibility_to_MDS/AML": 9,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|not_provided|Leukemia|_acute_myeloid|_susceptibility_to": 1,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|not_provided": 3,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Monocytopenia_with_susceptibility_to_infections|not_provided": 2,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|GATA2_deficiency_with_susceptibility_to_MDS/AML": 2,
    "Inborn_genetic_diseases|not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified": 4,
    "GATA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|Acute_myeloid_leukemia|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Hereditary_cancer-predisposing_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Monocytopenia_with_susceptibility_to_infections|GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome": 1,
    "Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment": 63,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Monocytopenia_with_susceptibility_to_infections": 2,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided|Myelodysplastic_syndrome|Acute_myeloid_leukemia|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Monocytopenia_with_susceptibility_to_infections": 9,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Monocytopenia_with_susceptibility_to_infections": 8,
    "Inborn_genetic_diseases|not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 4,
    "GATA2-related_disorder|GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|not_provided": 1,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases": 3,
    "GATA2-related_disorder|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2_deficiency_with_susceptibility_to_MDS/AML|not_provided|Leukemia|_acute_myeloid|_susceptibility_to": 1,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 4,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections": 2,
    "not_provided|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Myelodysplastic_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Leukemia|_acute_myeloid|_susceptibility_to": 1,
    "Myelodysplastic_syndrome|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Leukemia|_acute_myeloid|_susceptibility_to|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Myelodysplastic_syndrome|not_provided|Monocytopenia_with_susceptibility_to_infections": 1,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|not_provided": 5,
    "Leukemia|_acute_myeloid|_susceptibility_to|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia|Inborn_genetic_diseases": 3,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Monocytopenia_with_susceptibility_to_infections|not_specified": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided": 7,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|not_provided|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|Acute_myeloid_leukemia": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_specified|Inborn_genetic_diseases|Acute_myeloid_leukemia|GATA2-related_disorder|not_provided": 1,
    "Monocytopenia_with_susceptibility_to_infections|not_provided|Deafness-lymphedema-leukemia_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|Monocytopenia_with_susceptibility_to_infections|not_provided": 1,
    "not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 5,
    "Deafness-lymphedema-leukemia_syndrome|GATA2-related_disorder|Monocytopenia_with_susceptibility_to_infections": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|GATA2-related_disorder|GATA2_deficiency_with_susceptibility_to_MDS/AML|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|GATA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Anemia|Splenomegaly": 1,
    "Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome": 2,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided": 2,
    "GATA2-related_disorder|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases": 2,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2-related_disorder": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 2,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Leukemia|_acute_myeloid|_susceptibility_to|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia": 4,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|Acute_myeloid_leukemia|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Acute_myeloid_leukemia|not_specified|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome": 1,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Myelodysplastic_syndrome|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified": 1,
    "GATA2-related_disorder|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_specified|Acute_myeloid_leukemia": 1,
    "not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|Acute_myeloid_leukemia": 2,
    "GATA2-related_disorder|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|not_provided|not_specified|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases": 176,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2-related_disorder|Acute_myeloid_leukemia|Myelodysplastic_syndrome|not_specified": 1,
    "not_provided|Acute_myeloid_leukemia|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "not_specified|not_provided|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Acute_myeloid_leukemia|Inborn_genetic_diseases": 1,
    "GATA2-related_disorder|Inborn_genetic_diseases|not_provided|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|not_specified": 1,
    "not_provided|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases": 2,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|not_provided|Monocytopenia_with_susceptibility_to_infections": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|GATA2-related_disorder|Inborn_genetic_diseases|Myelodysplastic_syndrome|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome": 3,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia": 1,
    "not_provided|not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases": 1,
    "Acute_myeloid_leukemia|GATA2_deficiency_with_susceptibility_to_MDS/AML|Inborn_genetic_diseases": 1,
    "GATA2-related_disorder|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 3,
    "multilineage_dysplasia": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|Acute_myeloid_leukemia": 1,
    "not_provided|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "GATA2-related_disorder|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia|Myelodysplastic_syndrome": 1,
    "GATA2-related_disorder|not_provided|GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|Acute_myeloid_leukemia|not_specified": 1,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Myelodysplastic_syndrome|Acute_myeloid_leukemia|not_provided": 1,
    "not_provided|GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome": 2,
    "GATA2-related_disorder|Acute_myeloid_leukemia|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Predisposition_to_myelodysplastic_syndrome": 1,
    "Myelodysplastic_syndrome|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Acute_myeloid_leukemia": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Myelodysplastic_syndrome|Acute_myeloid_leukemia": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_specified|Inborn_genetic_diseases": 2,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2-related_disorder": 2,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Deafness-lymphedema-leukemia_syndrome|not_specified|Monocytopenia_with_susceptibility_to_infections": 1,
    "GATA2-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "GATA2_deficiency_with_susceptibility_to_MDS/AML|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|GATA2-related_disorder|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Acute_myeloid_leukemia": 1,
    "GATA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Acute_myeloid_leukemia|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Myelodysplastic_syndrome|not_provided|GATA2_deficiency_with_susceptibility_to_MDS/AML": 1,
    "not_provided|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Acute_myeloid_leukemia|GATA2-related_disorder|not_provided": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|not_provided|Myelodysplastic_syndrome": 1,
    "Monocytopenia_with_susceptibility_to_infections|Acute_myeloid_leukemia|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|not_provided": 1,
    "not_provided|Myelodysplastic_syndrome": 2,
    "Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2_deficiency_with_susceptibility_to_MDS/AML|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|Inborn_genetic_diseases|Acute_myeloid_leukemia|Myelodysplastic_syndrome": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Monocytopenia_with_susceptibility_to_infections|GATA2-related_disorder|Deafness-lymphedema-leukemia_syndrome|not_specified": 1,
    "Deafness-lymphedema-leukemia_syndrome|Inborn_genetic_diseases": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Deafness-lymphedema-leukemia_syndrome|not_provided|Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections": 1,
    "Inborn_genetic_diseases|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|not_provided|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|GATA2_deficiency_with_susceptibility_to_MDS/AML|not_provided": 1,
    "Inborn_genetic_diseases|GATA2_deficiency_with_susceptibility_to_MDS/AML|Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections": 1,
    "Inborn_genetic_diseases|not_provided|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Increased_risk_to_develop_myelodysplastic_syndrome|_acute_myeloid_leukemia|_or_chronic_myelomonocytic_leukemia": 1,
    "GATA2-related_disorder|not_specified|Acute_myeloid_leukemia|Monocytopenia_with_susceptibility_to_infections|Deafness-lymphedema-leukemia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Deafness-lymphedema-leukemia_syndrome|Monocytopenia_with_susceptibility_to_infections|GATA2-related_disorder|Acute_myeloid_leukemia": 1,
    "Monocytopenia_with_susceptibility_to_infections|not_specified|Inborn_genetic_diseases|Deafness-lymphedema-leukemia_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|GATA2-related_disorder|not_provided": 1,
    "Deafness-lymphedema-leukemia_syndrome|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2B": 124,
    "Charcot-Marie-Tooth_disease_type_2B|not_provided": 9,
    "Charcot-Marie-Tooth_disease_type_2B|not_specified": 2,
    "Charcot-Marie-Tooth_disease_type_2B|RAB7A-related_disorder|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|RAB7A-related_disorder|Charcot-Marie-Tooth_disease_type_2B|Inborn_genetic_diseases": 1,
    "Hereditary_sodium_channelopathy-related_small_fibers_neuropathy": 3,
    "Charcot-Marie-Tooth_disease_type_2B|RAB7A-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2B": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2B": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B": 4,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2B": 1,
    "Charcot-Marie-Tooth_disease_type_2B|not_specified|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2B|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2B|Charcot-Marie-Tooth_disease|not_provided": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2B": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2B": 4,
    "RAB7A-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2B": 1,
    "Charcot-Marie-Tooth_disease_type_2B|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2B|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2B|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2B|Inborn_genetic_diseases": 4,
    "Charcot-Marie-Tooth_disease_type_2B|RAB7A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Acyl-CoA_dehydrogenase_9_deficiency": 58,
    "Acyl-CoA_dehydrogenase_9_deficiency": 132,
    "Acyl-CoA_dehydrogenase_9_deficiency|not_provided": 43,
    "not_provided|not_specified|Acyl-CoA_dehydrogenase_9_deficiency": 3,
    "ACAD9-related_disorder": 3,
    "not_provided|ACAD9-related_disorder|Acyl-CoA_dehydrogenase_9_deficiency": 2,
    "not_provided|Inborn_genetic_diseases|Acyl-CoA_dehydrogenase_9_deficiency": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|Acyl-CoA_dehydrogenase_9_deficiency": 4,
    "Acyl-CoA_dehydrogenase_9_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Acyl-CoA_dehydrogenase_9_deficiency|not_provided": 2,
    "Mitochondrial_complex_I_deficiency|Acyl-CoA_dehydrogenase_9_deficiency": 2,
    "not_provided|Acyl-CoA_dehydrogenase_9_deficiency|not_specified": 4,
    "Acyl-CoA_dehydrogenase_9_deficiency|Mitochondrial_complex_I_deficiency|not_provided": 1,
    "Acyl-CoA_dehydrogenase_9_deficiency|ACAD9-related_disorder|not_provided|not_specified": 1,
    "ACAD9-related_disorder|Acyl-CoA_dehydrogenase_9_deficiency|not_provided": 2,
    "not_provided|Acyl-CoA_dehydrogenase_9_deficiency|ACAD9-related_disorder|Inborn_genetic_diseases": 1,
    "Acyl-CoA_dehydrogenase_9_deficiency|not_provided|not_specified": 3,
    "not_provided|ACAD9-related_disorder": 5,
    "Acyl-CoA_dehydrogenase_9_deficiency|not_specified|not_provided": 1,
    "Acyl-CoA_dehydrogenase_9_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "ACAD9-related_disorder|not_provided": 7,
    "Acyl-CoA_dehydrogenase_9_deficiency|ACAD9-related_disorder": 1,
    "not_specified|Acyl-CoA_dehydrogenase_9_deficiency|not_provided": 1,
    "not_specified|Acyl-CoA_dehydrogenase_9_deficiency": 2,
    "ACAD9-related_disorder|not_provided|Mitochondrial_complex_I_deficiency|Acyl-CoA_dehydrogenase_9_deficiency": 2,
    "Inborn_genetic_diseases|not_provided|Acyl-CoA_dehydrogenase_9_deficiency": 4,
    "ACAD9-related_disorder|not_specified|not_provided|Acyl-CoA_dehydrogenase_9_deficiency": 2,
    "ACAD9-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Acyl-CoA_dehydrogenase_9_deficiency": 3,
    "not_provided|Acyl-CoA_dehydrogenase_9_deficiency|ACAD9-related_disorder": 4,
    "Acyl-CoA_dehydrogenase_9_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Acyl-CoA_dehydrogenase_9_deficiency": 1,
    "Acyl-CoA_dehydrogenase_9_deficiency|not_provided|ACAD9-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|Acyl-CoA_dehydrogenase_9_deficiency|not_provided": 2,
    "Acyl-CoA_dehydrogenase_9_deficiency|not_specified|ACAD9-related_disorder|not_provided": 1,
    "not_specified|Acyl-CoA_dehydrogenase_9_deficiency|ACAD9-related_disorder|not_provided": 1,
    "not_specified|not_provided|ACAD9-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Acyl-CoA_dehydrogenase_9_deficiency|See_cases": 1,
    "Mitochondrial_complex_I_deficiency|not_provided|Acyl-CoA_dehydrogenase_9_deficiency": 1,
    "not_provided|Acyl-CoA_dehydrogenase_9_deficiency|Inborn_genetic_diseases": 2,
    "Bernard_Soulier_syndrome": 88,
    "Bernard_Soulier_syndrome|not_provided": 16,
    "not_provided|Bernard_Soulier_syndrome": 5,
    "Bernard-Soulier_syndrome_type_C|not_provided": 1,
    "not_provided|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome_type_C": 1,
    "Bernard-Soulier_syndrome_type_C": 2,
    "Bernard_Soulier_syndrome|not_specified|not_provided": 1,
    "GP9-related_disorder|Macrothrombocytopenia|not_provided|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome_type_C|Thrombocytopenia": 1,
    "Bernard_Soulier_syndrome|Inborn_genetic_diseases": 1,
    "Macrothrombocytopenia|not_provided|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome_type_C": 1,
    "not_provided|GP9-related_disorder|Bernard_Soulier_syndrome|not_specified": 1,
    "Bernard_Soulier_syndrome|not_specified": 3,
    "Thrombocytopenia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|GP9-related_disorder|Bernard_Soulier_syndrome|Inborn_genetic_diseases": 1,
    "Macrothrombocytopenia|Bernard_Soulier_syndrome": 2,
    "not_specified|not_provided|Bernard_Soulier_syndrome": 4,
    "GP9-related_disorder|Bernard_Soulier_syndrome|not_provided": 1,
    "GP9-related_disorder": 2,
    "GP9-related_disorder|not_provided|Bernard_Soulier_syndrome": 1,
    "not_provided|GP9-related_disorder": 2,
    "Bernard_Soulier_syndrome|not_provided|not_specified": 1,
    "not_specified|Bernard_Soulier_syndrome|not_provided": 2,
    "RAB43-related_disorder": 7,
    "CNBP-related_disorder": 6,
    "Myotonic_dystrophy_type_2|CNBP-related_disorder|not_provided": 1,
    "Myotonic_dystrophy_type_2": 1,
    "Immunodeficiency_128": 1,
    "Melanoma|_uveal|_susceptibility_to|_1|not_provided": 1,
    "Melanoma|_uveal|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided|Tumor_predisposition_syndrome_2": 1,
    "MBD4-related_disorder": 2,
    "Melanoma|_uveal|_susceptibility_to|_1|Tumor_predisposition_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|MBD4-related_disorder": 2,
    "Melanoma|_uveal|_susceptibility_to|_1|not_provided|MBD4-related_disorder|Tumor_predisposition_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "MBD4-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Melanoma|_uveal|_susceptibility_to|_1": 1,
    "MBD4-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|MBD4-related_disorder": 2,
    "Melanoma|_uveal|_susceptibility_to|_1|Tumor_predisposition_syndrome_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "MBD4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "MBD4-related_disorder|not_provided": 1,
    "Tumor_predisposition_syndrome_2|not_specified|not_provided|Melanoma|_uveal|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|O'Donnell-Luria-Rodan_syndrome": 2,
    "not_provided|MBD4-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Tumor_predisposition_syndrome_2": 2,
    "Tumor_predisposition_syndrome_2|Melanoma|_uveal|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases": 1,
    "MBD4-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Melanoma|_uveal|_susceptibility_to|_1|Tumor_predisposition_syndrome_2": 2,
    "not_specified|MBD4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Cranioectodermal_dysplasia_1": 21,
    "Cranioectodermal_dysplasia_1": 600,
    "Cranioectodermal_dysplasia_1|not_provided": 16,
    "Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_1": 38,
    "Cranioectodermal_dysplasia_1|Inborn_genetic_diseases": 25,
    "Inborn_genetic_diseases|not_provided|Cranioectodermal_dysplasia_1": 4,
    "Cranioectodermal_dysplasia_1|IFT122-related_disorder": 3,
    "IFT122-related_disorder|Cranioectodermal_dysplasia_1": 4,
    "not_specified|Connective_tissue_disorder|Cranioectodermal_dysplasia|not_provided|Cranioectodermal_dysplasia_1": 1,
    "Cranioectodermal_dysplasia_1|Connective_tissue_disorder": 4,
    "not_specified|Cranioectodermal_dysplasia_1": 1,
    "IFT122-related_disorder": 3,
    "Inborn_genetic_diseases|Connective_tissue_disorder": 2,
    "Cranioectodermal_dysplasia_1|not_provided|not_specified|IFT122-related_disorder|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|Cranioectodermal_dysplasia_1": 2,
    "not_provided|Cranioectodermal_dysplasia_1|Cranioectodermal_dysplasia|not_specified": 3,
    "not_provided|not_specified|Cranioectodermal_dysplasia_1": 2,
    "Connective_tissue_disorder|not_specified|not_provided|Cranioectodermal_dysplasia_1|Rod-cone_dystrophy": 1,
    "Cranioectodermal_dysplasia_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_1|not_provided": 2,
    "Connective_tissue_disorder|not_specified|not_provided|Cranioectodermal_dysplasia_1": 2,
    "Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_1": 1,
    "not_provided|Cranioectodermal_dysplasia_1|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_1|not_specified": 2,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_1|not_specified": 1,
    "not_specified|not_provided|Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_1": 1,
    "not_provided|Connective_tissue_disorder|Cranioectodermal_dysplasia_1|Cranioectodermal_dysplasia": 1,
    "Cranioectodermal_dysplasia_1|not_provided|Connective_tissue_disorder|not_specified": 1,
    "Cranioectodermal_dysplasia_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Cranioectodermal_dysplasia_1|IFT122-related_disorder": 1,
    "not_specified|not_provided|Cranioectodermal_dysplasia_1": 2,
    "not_provided|not_specified|Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_1": 1,
    "not_provided|Connective_tissue_disorder|Cranioectodermal_dysplasia_1": 3,
    "Cranioectodermal_dysplasia_1|IFT122-related_disorder|not_specified": 1,
    "not_provided|Cranioectodermal_dysplasia_1|Connective_tissue_disorder": 1,
    "Cranioectodermal_dysplasia|not_provided|Cranioectodermal_dysplasia_1": 1,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_1": 1,
    "Connective_tissue_disorder|not_provided|Cranioectodermal_dysplasia_1": 1,
    "not_specified|Cranioectodermal_dysplasia_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cranioectodermal_dysplasia_1": 2,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_1|Connective_tissue_disorder": 1,
    "Cranioectodermal_dysplasia_1|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Cranioectodermal_dysplasia_1|IFT122-related_disorder|not_specified": 1,
    "IFT122-related_disorder|Cranioectodermal_dysplasia_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Connective_tissue_disorder|not_provided|Cranioectodermal_dysplasia_1": 1,
    "not_provided|IFT122-related_disorder|Cranioectodermal_dysplasia_1|Microcephaly": 1,
    "not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_1": 9,
    "not_provided|Retinitis_pigmentosa|not_specified|Retinitis_pigmentosa_4|Pigmentary_retinal_dystrophy|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_1": 42,
    "Retinitis_pigmentosa_4|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 2,
    "not_provided|Retinitis_pigmentosa_4": 19,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_4": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_4": 2,
    "Retinitis_pigmentosa_4": 26,
    "Retinitis_pigmentosa|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1": 6,
    "Retinitis_pigmentosa_4|not_provided|RHO-related_disorder|Pigmentary_retinal_dystrophy|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_4|not_provided": 9,
    "RHO-related_disorder|Retinitis_pigmentosa_4|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_4|not_provided": 5,
    "Retinitis_pigmentosa_4|not_provided|RHO-related_disorder|Retinal_dystrophy": 1,
    "Microcephaly_17|_primary|_autosomal_recessive|not_provided|Occult_macular_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_4|Retinal_dystrophy": 3,
    "Congenital_stationary_night_blindness_autosomal_dominant_1": 4,
    "not_provided|Congenital_stationary_night_blindness|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_4": 2,
    "RHO-related_disorder|not_provided": 2,
    "Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_4": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_4": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_1|Pigmentary_retinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|See_cases|not_provided|Retinitis_pigmentosa_4": 1,
    "Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1|Pigmentary_retinal_dystrophy|not_provided|Retinal_dystrophy|RHO-related_disorder": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_4|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_4|not_provided|Retinal_dystrophy": 6,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_4": 3,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa_4": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Retinitis_Pigmentosa|_Dominant/Recessive|Congenital_Stationary_Night_Blindness|_Dominant|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa_4": 1,
    "Retinitis_pigmentosa|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1|not_specified": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_4": 4,
    "not_provided|Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa": 1,
    "not_provided|RHO-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_4|Retinitis_punctata_albescens": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_4|_autosomal_recessive|Retinitis_pigmentosa_4|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Retinitis_pigmentosa_4|_autosomal_recessive|Retinitis_pigmentosa_4|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1|not_provided|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_4|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_4": 2,
    "Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_1|not_provided": 1,
    "RHO-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_4": 1,
    "Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinal_dystrophy|not_provided|Pigmentary_retinal_dystrophy": 1,
    "not_specified|not_provided|RHO-related_disorder|Retinitis_pigmentosa_4": 1,
    "Retinitis_pigmentosa_4|Retinal_dystrophy|not_provided": 4,
    "Retinitis_pigmentosa|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Retinitis_pigmentosa_4|Retinal_dystrophy": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa_4|Pigmentary_retinal_dystrophy|not_provided": 1,
    "Optic_atrophy|RHO-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_provided|RHO-related_disorder": 2,
    "not_provided|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1|not_specified": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_4|_autosomal_recessive|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "not_provided|Cone_dystrophy_3|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_4|Pigmentary_retinal_dystrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_4": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_4": 1,
    "Retinitis_pigmentosa_4|Retinitis_pigmentosa": 1,
    "Exudative_retinopathy|Cataract|Retinal_detachment|Blindness|Optic_disc_drusen|Abnormality_of_retinal_pigmentation|Monocular_strabismus|Rod-cone_dystrophy|Progressive_visual_loss|Retinal_exudate|Nystagmus|not_provided|Pigmentary_retinal_dystrophy": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_1|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Pigmentary_retinal_dystrophy": 14,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_4": 2,
    "Retinitis_pigmentosa|not_provided|RHO-related_disorder|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinal_dystrophy": 1,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_4|not_specified|not_provided": 1,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Retinal_disorders|RHO-related_disorder|Microcephaly_17|_primary|_autosomal_recessive|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_4|Night_blindness|Peripheral_visual_field_loss|Blurred_vision": 1,
    "not_specified|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_4|Congenital_stationary_night_blindness_autosomal_dominant_1": 1,
    "Congenital_Stationary_Night_Blindness|_Dominant|Retinitis_Pigmentosa|_Dominant/Recessive": 1,
    "Congenital_Stationary_Night_Blindness|_Dominant|Retinitis_Pigmentosa|_Dominant/Recessive|not_provided": 1,
    "Retinitis_Pigmentosa|_Dominant/Recessive|Congenital_Stationary_Night_Blindness|_Dominant": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_1|Retinitis_pigmentosa": 1,
    "PLXND1-related_disorder": 24,
    "Congenital_heart_defects|_multiple_types|_9|Kleine-Levin_syndrome": 1,
    "PLXND1-related_disorder|not_provided": 14,
    "Congenital_heart_defects|_multiple_types|_9": 6,
    "not_specified|not_provided|Congenital_heart_defects|_multiple_types|_9": 1,
    "not_provided|PLXND1-related_disorder": 17,
    "not_specified|PLXND1-related_disorder": 2,
    "not_specified|not_provided|PLXND1-related_disorder": 1,
    "Oromandibular-limb_hypogenesis_spectrum|not_specified": 1,
    "Congenital_heart_defects|_multiple_types|_9|PLXND1-related_disorder|not_provided": 1,
    "not_specified|Congenital_heart_defects|_multiple_types|_9": 1,
    "Kleine-Levin_syndrome|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_9|not_provided": 1,
    "not_provided|not_specified|PLXND1-related_disorder": 1,
    "TRH-related_disorder": 4,
    "not_provided|not_specified|Hypothalamic_hypothyroidism": 1,
    "not_specified|Hypothalamic_hypothyroidism|not_provided": 1,
    "Hypothalamic_hypothyroidism": 1,
    "not_specified|not_provided|Hypothalamic_hypothyroidism": 1,
    "COL6A5-related_disorder": 7,
    "not_specified|COL6A5-related_disorder|not_provided": 1,
    "COL6A5-related_disorder|not_provided": 1,
    "COL6A5-related_disorder|not_provided|COL6A5_POLYMORPHISM": 1,
    "COL6A6-related_disorder": 3,
    "ATP2C1-related_disorder": 5,
    "Familial_benign_pemphigus": 69,
    "Familial_benign_pemphigus|not_provided": 11,
    "Familial_benign_pemphigus|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Familial_benign_pemphigus": 1,
    "not_provided|Familial_benign_pemphigus": 5,
    "not_provided|ATP2C1-related_disorder": 2,
    "Familial_benign_pemphigus|Inborn_genetic_diseases": 1,
    "ATP2C1-related_disorder|Familial_benign_pemphigus|not_provided": 1,
    "ATP2C1-related_disorder|not_specified": 1,
    "ATP2C1-related_disorder|Familial_benign_pemphigus|not_provided|not_specified": 1,
    "ASTE1-related_disorder": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_9": 2,
    "MRPL3-related_disorder|not_provided": 1,
    "not_provided|MRPL3-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_9": 5,
    "MRPL3-related_disorder": 2,
    "DNAJC13-related_disorder": 19,
    "not_specified|DNAJC13-related_disorder": 1,
    "DNAJC13-related_disorder|not_specified|not_provided": 2,
    "DNAJC13-related_disorder|not_provided": 5,
    "Essential_tremor|Parkinson_disease_21|Parkinson_disease|_late-onset": 1,
    "not_provided|DNAJC13-related_disorder": 8,
    "Parkinson_disease_21|not_provided": 1,
    "not_provided|DNAJC13-related_disorder|not_specified": 1,
    "DNAJC13-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_44|not_specified": 1,
    "UBA5-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_44": 16,
    "UBA5-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_44": 5,
    "Developmental_and_epileptic_encephalopathy|_44|not_provided": 3,
    "Spinocerebellar_ataxia|_autosomal_recessive_24|Developmental_and_epileptic_encephalopathy|_44|not_provided|UBA5-related_disorder": 1,
    "not_provided|UBA5-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_44|Spinocerebellar_ataxia|_autosomal_recessive_24": 2,
    "Developmental_and_epileptic_encephalopathy|_44|not_provided|Spinocerebellar_ataxia|_autosomal_recessive_24": 1,
    "UBA5-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive_24": 1,
    "Developmental_and_epileptic_encephalopathy|_44|Spinocerebellar_ataxia|_autosomal_recessive_24|not_provided": 1,
    "UBA5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "UBA5-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "UBA5-related_disorder|Developmental_and_epileptic_encephalopathy|_44": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_24": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_44|Spinocerebellar_ataxia|_autosomal_recessive_24": 1,
    "Developmental_and_epileptic_encephalopathy|_44|Spinocerebellar_ataxia|_autosomal_recessive_24|UBA5-related_disorder|Intellectual_disability|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 23,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|not_provided|Nephronophthisis_3": 3,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|not_provided": 2,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|Meckel-Gruber_syndrome": 4,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|not_provided|Meckel-Gruber_syndrome": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|not_provided|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 84,
    "Nephronophthisis|not_provided|Kidney_disorder|not_specified": 1,
    "not_specified|Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "Kidney_disorder|not_specified|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis|not_provided": 1,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder|Nephronophthisis": 1,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|not_provided|Nephronophthisis": 1,
    "Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 11,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|not_provided|NPHP3-related_disorder|Nephronophthisis": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Nephronophthisis_3|not_provided": 1,
    "Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 5,
    "Nephronophthisis|NPHP3-related_disorder|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided": 1,
    "NPHP3-related_disorder|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 9,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_disorder": 1,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis": 2,
    "Nephronophthisis_3": 12,
    "Inborn_genetic_diseases|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|not_provided|not_specified|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "NPHP3-related_disorder|Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "not_provided|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 2,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 12,
    "not_specified|Nephronophthisis|not_provided|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Nephronophthisis|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 9,
    "NPHP3-related_disorder|not_provided|Nephronophthisis": 4,
    "Nephronophthisis|not_provided|NPHP3-related_disorder": 5,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 10,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis": 3,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|Kidney_disorder|not_provided|not_specified": 1,
    "not_provided|Optic_atrophy|Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|not_specified": 1,
    "Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 2,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis": 7,
    "Nephronophthisis|NPHP3-related_disorder|not_provided": 2,
    "Nephronophthisis|NPHP3-related_disorder": 6,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis": 9,
    "not_specified|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis|Kidney_disorder": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "Optic_atrophy|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Nephronophthisis_3|NPHP3-related_disorder|not_provided": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Nephronophthisis_3|not_provided": 1,
    "not_specified|Nephronophthisis|not_provided|Bardet-Biedl_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided|Nephronophthisis": 2,
    "not_provided|Kidney_disorder|Nephronophthisis|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Renal_dysplasia_and_retinal_aplasia|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|NPHP3-related_disorder": 1,
    "not_provided|Nephronophthisis|not_specified|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "Renal-hepatic-pancreatic_dysplasia_1": 4,
    "NPHP3-related_disorder|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Inborn_genetic_diseases": 1,
    "Fibrotic_kidney_disease|Nephronophthisis|not_provided": 1,
    "Enlarged_kidney|Multiple_renal_cysts|Anhydramnios": 3,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder": 1,
    "Nephronophthisis|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder": 2,
    "NPHP3-related_disorder": 29,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|not_provided": 3,
    "NPHP3-related_Meckel-like_syndrome": 3,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 3,
    "not_provided|Kidney_disorder|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis|Inborn_genetic_diseases": 1,
    "not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 2,
    "Nephronophthisis|not_specified|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 2,
    "not_specified|not_provided|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 2,
    "Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_disorder": 1,
    "NPHP3-related_disorder|Nephronophthisis|not_specified|not_provided": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Inborn_genetic_diseases|Nephronophthisis": 1,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|not_provided": 3,
    "not_specified|not_provided|Kidney_disorder|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis|Inborn_genetic_diseases|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 1,
    "NPHP3-related_disorder|Nephronophthisis|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 1,
    "NPHP3-related_disorder|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_disorder": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|not_specified|not_provided|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis|Joubert_syndrome_and_related_disorders": 1,
    "not_specified|Kidney_disorder|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_provided": 1,
    "not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis|NPHP3-related_disorder": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_provided": 1,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 4,
    "NPHP3-related_disorder|Nephronophthisis": 7,
    "Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_provided|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|NPHP3-related_disorder": 1,
    "Joubert_syndrome_and_related_disorders|NPHP3-related_disorder": 1,
    "Nephronophthisis|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|not_specified": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_specified": 1,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|not_provided": 1,
    "NPHP3-related_disorder|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 2,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided": 1,
    "NPHP3-related_disorder|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|NPHP3-related_Meckel-like_syndrome": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Inborn_genetic_diseases": 1,
    "Nephronophthisis|not_specified|not_provided|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 2,
    "Inborn_genetic_diseases|not_provided|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis": 1,
    "Renal-hepatic-pancreatic_dysplasia": 2,
    "not_provided|NPHP3-related_disorder|Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Polycystic_kidney_disease": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|not_specified|Nephronophthisis": 2,
    "Renal-hepatic-pancreatic_dysplasia_1|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_specified|not_provided|Nephronophthisis": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis|Focal_segmental_glomerulosclerosis|not_provided|not_specified": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Nephronophthisis_3": 3,
    "not_provided|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 2,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 2,
    "Inborn_genetic_diseases|NPHP3-related_disorder|Nephronophthisis": 1,
    "NPHP3-related_disorder|Nephronophthisis|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Joubert_syndrome_and_related_disorders|not_provided": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_provided|Nephronophthisis": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|not_specified": 1,
    "NPHP3-related_disorder|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_provided": 3,
    "not_specified|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Inborn_genetic_diseases|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 3,
    "NPHP3-related_disorder|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Inborn_genetic_diseases|Nephronophthisis": 3,
    "Inborn_genetic_diseases|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|not_provided": 1,
    "NPHP3-related_disorder|not_provided|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis": 1,
    "Retinal_dystrophy|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Nephronophthisis_3|NPHP3-related_disorder": 1,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|not_provided|NPHP3-related_disorder|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Nephronophthisis_3|Nephronophthisis|not_provided|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome|NPHP3-related_disorder|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis|not_provided|Inborn_genetic_diseases|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 1,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 1,
    "NPHP3-related_disorder|Joubert_syndrome_and_related_disorders|Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_provided|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Retinal_dystrophy": 1,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|not_specified|Nephronophthisis": 1,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "Nephronophthisis_3|Nephronophthisis": 1,
    "not_provided|Joubert_syndrome_and_related_disorders": 3,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_provided|NPHP3-related_disorder|Nephronophthisis": 2,
    "Nephronophthisis|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_provided": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Nephronophthisis|not_provided|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder": 1,
    "NPHP3-related_disorder|NPHP3-related_Meckel-like_syndrome|not_provided|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis": 3,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder|Inborn_genetic_diseases": 1,
    "Fibrotic_kidney_disease": 1,
    "Inborn_genetic_diseases|NPHP3-related_disorder": 3,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Joubert_syndrome_and_related_disorders|Nephronophthisis": 1,
    "not_specified|Renal-hepatic-pancreatic_dysplasia_1|Meckel-Gruber_syndrome|not_provided|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|NPHP3-related_disorder": 3,
    "Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 2,
    "Nephronophthisis_3|not_provided|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Joubert_syndrome_and_related_disorders|Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder": 1,
    "Nephronophthisis|not_specified|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome": 1,
    "not_provided|Nephronophthisis|NPHP3-related_disorder|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Inborn_genetic_diseases|Nephronophthisis_3|not_provided|not_specified|Nephronophthisis": 1,
    "NPHP3-related_disorder|Nephronophthisis|not_specified|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|See_cases": 1,
    "Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis|not_provided": 1,
    "not_provided|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 2,
    "Nephronophthisis|Nephronophthisis_3": 2,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Inborn_genetic_diseases": 1,
    "NPHP3-related_disorder|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_provided|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "NPHP3-related_disorder|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|not_provided": 1,
    "not_specified|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "not_provided|Kidney_disorder|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|not_specified": 1,
    "Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Kidney_disorder": 1,
    "NPHP3-related_disorder|Inborn_genetic_diseases|Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_provided": 1,
    "Nephronophthisis|not_provided|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 2,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|NPHP3-related_disorder": 1,
    "Nephronophthisis|not_specified|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "not_provided|not_specified|Nephronophthisis|NPHP3-related_disorder": 1,
    "Nephronophthisis|Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis|not_provided|NPHP3-related_disorder": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_provided": 1,
    "Nephronophthisis|NPHP3-related_disorder|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Kidney_disorder|not_provided|not_specified|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Nephronophthisis": 1,
    "Kidney_disorder|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_specified|not_provided|Nephronophthisis": 1,
    "not_provided|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis": 1,
    "NPHP3-related_disorder|Nephronophthisis|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|not_specified|not_provided|Nephronophthisis": 1,
    "not_provided|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|not_provided|Inborn_genetic_diseases|Nephronophthisis": 1,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_provided|NPHP3-related_disorder|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Inborn_genetic_diseases": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|not_provided|Nephronophthisis_3": 1,
    "not_provided|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis|not_specified": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|Nephronophthisis|not_provided": 1,
    "Retinal_dystrophy|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_provided|Nephronophthisis": 1,
    "Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|not_provided|Nephronophthisis": 1,
    "Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|NPHP3-related_disorder|Nephronophthisis": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3": 1,
    "NPHP3-related_disorder|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|NPHP3-related_disorder|Renal-hepatic-pancreatic_dysplasia_1|NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|not_provided|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome": 1,
    "Nephronophthisis|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|not_provided|Inborn_genetic_diseases|NPHP3-related_disorder": 1,
    "not_provided|NPHP3-related_Meckel-like_syndrome|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|Nephronophthisis|NPHP3-related_disorder|Inborn_genetic_diseases": 1,
    "Kidney_disorder|Nephronophthisis|not_provided|Renal-hepatic-pancreatic_dysplasia_1|Nephronophthisis_3|NPHP3-related_Meckel-like_syndrome|not_specified": 1,
    "NPHP3-related_Meckel-like_syndrome|Nephronophthisis_3|Renal-hepatic-pancreatic_dysplasia_1": 1,
    "NPHP3-related_disorder|Nephronophthisis|not_provided|Renal-hepatic-pancreatic_dysplasia_1|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Renal-hepatic-pancreatic_dysplasia_1|Meckel-Gruber_syndrome": 1,
    "Cataract_12_multiple_types": 40,
    "Cataract_12_multiple_types|BFSP2-related_disorder": 3,
    "not_provided|Cataract_12_multiple_types": 3,
    "Cataract_12_multiple_types|not_specified": 6,
    "Cataract_12_multiple_types|not_provided": 8,
    "not_specified|Cataract_12_multiple_types": 3,
    "Global_developmental_delay|Seizure|Cataract|Nystagmus|Strabismus|Abnormal_thorax_morphology|Intellectual_disability": 1,
    "BFSP2-related_disorder|not_provided|Cataract_12_multiple_types": 1,
    "BFSP2-related_disorder|not_specified": 1,
    "BFSP2-related_disorder|Cataract_12_multiple_types": 1,
    "BFSP2-related_disorder": 1,
    "not_provided|not_specified|Cataract_12_multiple_types": 1,
    "Cataract_12_multiple_types|not_provided|not_specified": 1,
    "TOPBP1-related_disorder": 18,
    "TOPBP1-related_disorder|not_provided": 1,
    "not_provided|TOPBP1-related_disorder": 1,
    "not_specified|TOPBP1-related_disorder": 1,
    "Pulmonary_arterial_hypertension|not_specified": 1,
    "Atransferrinemia": 33,
    "not_provided|Atransferrinemia": 17,
    "not_provided|Atransferrinemia|not_specified": 1,
    "Atransferrinemia|not_provided": 9,
    "not_provided|TF-related_disorder|Atransferrinemia": 2,
    "Atransferrinemia|not_specified": 3,
    "TF-related_disorder|not_provided|Atransferrinemia": 3,
    "not_provided|not_specified|Atransferrinemia": 1,
    "TF-related_disorder|Atransferrinemia|not_provided": 1,
    "Atransferrinemia|TF-related_disorder|not_provided|Iron_deficiency_anemia": 1,
    "Transferrin_variant_D1": 1,
    "Atransferrinemia|Transferrin_variant_D(Chi)|not_provided": 1,
    "TF-related_disorder": 1,
    "not_specified|not_provided|Atransferrinemia": 1,
    "Atransferrinemia|TF-related_disorder|not_provided": 1,
    "not_specified|Atransferrinemia": 2,
    "TF*C2|Atransferrinemia|not_provided": 1,
    "not_provided|TF-related_disorder": 1,
    "Transferrin_variant_Bv": 1,
    "TF-related_disorder|not_specified|not_provided|Transferrin_variant_B2|Atransferrinemia": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2": 35,
    "not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2|Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant": 2,
    "not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2": 8,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2|not_provided": 5,
    "not_provided|SLCO2A1-related_disorder": 5,
    "SLCO2A1-related_disorder|not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2": 1,
    "SLCO2A1-related_disorder": 3,
    "Inborn_genetic_diseases|SLCO2A1-related_disorder|not_provided": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2|Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant": 2,
    "SLCO2A1-related_disorder|not_provided": 3,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2|Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant|not_provided": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2|not_specified|Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant|not_provided": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant|not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_dominant|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_2|not_provided": 1,
    "Pachydermoperiostosis_syndrome": 1,
    "not_specified|RYK-related_disorder": 2,
    "RYK-related_disorder": 5,
    "not_provided|RYK-related_disorder": 1,
    "CEP63-related_disorder|not_provided": 2,
    "not_specified|not_provided|Seckel_syndrome_6": 1,
    "Developmental_dyslexia": 2,
    "not_provided|Seckel_syndrome_6": 2,
    "not_specified|Seckel_syndrome_6|not_provided": 1,
    "CEP63-related_disorder": 1,
    "not_specified|not_provided|CEP63-related_disorder": 1,
    "not_provided|Seckel_syndrome_6|Inborn_genetic_diseases": 1,
    "not_provided|CEP63-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Seckel_syndrome_6": 1,
    "Seckel_syndrome_6|not_provided": 1,
    "Inborn_genetic_diseases|Myofibrillar_myopathy_7": 4,
    "KY-related_disorder": 7,
    "Myofibrillar_myopathy_7": 12,
    "Myofibrillar_myopathy_7|not_provided": 5,
    "not_provided|KY-related_disorder": 3,
    "KY-related_disorder|not_provided": 3,
    "Myofibrillar_myopathy_7|Inborn_genetic_diseases": 2,
    "KY-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_7": 3,
    "Inborn_genetic_diseases|not_provided|KY-related_disorder": 1,
    "PPP2R3A-related_disorder": 39,
    "not_provided|PPP2R3A-related_disorder": 1,
    "Karayol-Borroto-Haghshenas_neurodevelopmental_syndrome": 5,
    "Karayol-Borroto-Haghshenas_neurodevelopmental_syndrome|Syndromic_neurodevelopmental_disorder|not_provided": 1,
    "Karayol-Borroto-Haghshenas_neurodevelopmental_syndrome|not_provided|Syndromic_neurodevelopmental_disorder": 1,
    "Autism|Karayol-Borroto-Haghshenas_neurodevelopmental_syndrome": 1,
    "Syndromic_neurodevelopmental_disorder": 5,
    "Propionic_acidemia": 2190,
    "Propionic_acidemia|not_provided|not_specified": 7,
    "not_provided|Propionic_acidemia": 54,
    "Inborn_genetic_diseases|Propionic_acidemia": 44,
    "not_specified|Propionic_acidemia": 29,
    "Propionic_acidemia|not_specified": 24,
    "Propionic_acidemia|Inborn_genetic_diseases": 30,
    "not_provided|PCCB-related_disorder|Propionic_acidemia|not_specified": 1,
    "Propionic_acidemia|not_provided": 49,
    "Propionic_acidemia|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|Propionic_acidemia": 6,
    "not_specified|Inborn_genetic_diseases|Propionic_acidemia": 2,
    "PCCB-related_disorder|not_provided|Propionic_acidemia": 6,
    "PCCB-related_disorder|not_provided|Propionic_acidemia|not_specified": 1,
    "PCCB-related_disorder": 2,
    "not_provided|Propionic_acidemia|Abnormality_of_metabolism/homeostasis": 1,
    "PCCB-related_disorder|Propionic_acidemia|not_provided": 4,
    "not_specified|not_provided|Propionic_acidemia": 7,
    "Propionic_acidemia|PCCB-related_disorder": 7,
    "Inborn_genetic_diseases|not_provided|Propionic_acidemia": 7,
    "Inborn_genetic_diseases|not_specified|not_provided|Propionic_acidemia": 1,
    "PCCB-related_disorder|Propionic_acidemia|Hyperammonemia|Global_developmental_delay": 1,
    "PCCB-related_disorder|Propionic_acidemia": 4,
    "not_provided|Propionic_acidemia|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Propionic_acidemia|not_provided": 2,
    "not_provided|Propionic_acidemia|not_specified": 2,
    "PCCB-related_disorder|Inborn_genetic_diseases|not_provided|Propionic_acidemia": 1,
    "not_specified|Propionic_acidemia|Inborn_genetic_diseases": 2,
    "Hypertrophic_cardiomyopathy|Propionic_acidemia|not_provided": 1,
    "Global_developmental_delay|Hyperammonemia|PCCB-related_disorder|not_provided|Propionic_acidemia": 1,
    "Propionic_acidemia|not_specified|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_47": 43,
    "STAG1-related_disorder": 11,
    "STAG1-related_disorder|Intellectual_disability|_autosomal_dominant_47|not_specified|not_provided": 1,
    "STAG1-related_disorder|Intellectual_disability|_autosomal_dominant_47|Inborn_genetic_diseases": 1,
    "not_provided|STAG1-related_disorder": 3,
    "STAG1-related_disorder|not_provided": 6,
    "Intellectual_disability|_autosomal_dominant_47|not_provided": 9,
    "not_provided|Intellectual_disability|_autosomal_dominant_47": 2,
    "STAG1-related_disorder|Congenital_ocular_coloboma|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_47|Intellectual_disability|STAG1-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_47": 1,
    "Intellectual_disability|_autosomal_dominant_47|STAG1-related_disorder": 3,
    "not_provided|STAG1-related_disorder|Intellectual_disability|_autosomal_dominant_47|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|STAG1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_dominant_47|not_provided": 1,
    "not_provided|DZIP1L-related_disorder": 10,
    "DZIP1L-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "DZIP1L-related_disorder|not_provided": 9,
    "DZIP1L-related_disorder": 11,
    "Polycystic_kidney_disease_5": 9,
    "Polycystic_kidney_disease_5|not_provided": 4,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_5": 1,
    "DZIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Polycystic_kidney_disease_5": 2,
    "DZIP1L-related_disorder|Polycystic_kidney_disease_5": 1,
    "not_provided|DBR1-related_disorder": 2,
    "DBR1-related_disorder": 1,
    "Encephalitis|_acute|_infection_(viral)-induced|_susceptibility_to|_11": 4,
    "not_provided|Encephalitis|_acute|_infection_(viral)-induced|_susceptibility_to|_11": 3,
    "Xerosis_and_growth_failure_with_immune_and_pulmonary_dysfunction_syndrome|Encephalitis|_acute|_infection_(viral)-induced|_susceptibility_to|_11": 1,
    "not_specified|MRAS-related_disorder": 1,
    "Noonan_syndrome_11|not_provided": 2,
    "Noonan_syndrome_11|not_provided|RASopathy": 2,
    "Noonan_syndrome_11": 1,
    "RASopathy|not_provided|MRAS-related_disorder": 1,
    "not_provided|MRAS-related_disorder|Inborn_genetic_diseases": 2,
    "Noonan_syndrome_11|RASopathy": 1,
    "Inborn_genetic_diseases|Noonan_syndrome_11|not_provided": 1,
    "MRAS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RASopathy|not_provided|Inborn_genetic_diseases|MRAS-related_disorder": 1,
    "RASopathy|MRAS-related_disorder|not_provided": 1,
    "not_specified|MRAS-related_disorder|not_provided": 1,
    "Median_cleft_lip_and_palate": 3,
    "not_specified|FOXL2-related_disorder|not_provided": 2,
    "FOXL2-related_disorder": 8,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome": 102,
    "not_provided|FOXL2-related_disorder": 2,
    "not_specified|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3|Genetic_non-acquired_premature_ovarian_failure": 1,
    "Premature_ovarian_failure_3": 4,
    "BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I": 4,
    "Blepharophimosis": 1,
    "BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I|not_provided|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome": 1,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_II": 2,
    "FOXL2-related_disorder|not_provided|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3": 1,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_II|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I": 1,
    "Inborn_genetic_diseases|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_II|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I|not_provided": 1,
    "not_provided|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome": 5,
    "Premature_ovarian_failure_3|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|not_provided": 2,
    "FOXL2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_II|not_provided|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Blepharophimosis|_ptosis|_and_epicanthus_inversus|_type_II_with_Duane_retraction_syndrome": 1,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_II": 1,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3": 4,
    "not_provided|Premature_ovarian_failure_3": 1,
    "BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I|Premature_ovarian_failure_3|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|not_provided": 1,
    "not_provided|FOXL2-related_disorder|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome": 1,
    "Premature_ovarian_failure_3|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome": 1,
    "not_provided|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Premature_ovarian_failure_3|See_cases": 1,
    "not_specified|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|not_provided": 1,
    "not_provided|not_specified|Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome": 1,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|not_provided": 4,
    "not_provided|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I": 2,
    "FOXL2-related_disorder|BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_I": 1,
    "Blepharophimosis|_ptosis|_and_epicanthus_inversus_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Premature_ovarian_failure_3": 1,
    "BLEPHAROPHIMOSIS|_PTOSIS|_AND_EPICANTHUS_INVERSUS|_TYPE_II": 1,
    "not_specified|Hypotonia_with_lactic_acidemia_and_hyperammonemia|not_provided": 1,
    "Ovarian_dysgenesis_7": 1,
    "MRPS22-related_disorder|not_provided": 3,
    "Hypotonia_with_lactic_acidemia_and_hyperammonemia": 15,
    "not_specified|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "Hypotonia_with_lactic_acidemia_and_hyperammonemia|Inborn_genetic_diseases|not_provided": 1,
    "Hypotonia_with_lactic_acidemia_and_hyperammonemia|Inborn_genetic_diseases": 1,
    "Hypotonia_with_lactic_acidemia_and_hyperammonemia|not_provided": 3,
    "MRPS22-related_disorder": 5,
    "MRPS22-related_disorder|not_specified|not_provided|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "not_specified|not_provided|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "Ovarian_dysgenesis_7|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "MRPS22-related_disorder|not_provided|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 4,
    "not_provided|not_specified|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "not_provided|MRPS22-related_disorder": 1,
    "Premature_ovarian_failure|Ovarian_dysgenesis_7": 1,
    "Hypotonia_with_lactic_acidemia_and_hyperammonemia|not_provided|Ovarian_dysgenesis_7": 1,
    "Ovarian_dysgenesis_7|46_XX_gonadal_dysgenesis|not_provided|Muscular_dystrophy|_adult-onset|_with_leukoencephalopathy": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency": 2,
    "not_provided|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 3,
    "Mitochondrial_disease|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Mitochondrial_disease|not_provided|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "Combined_oxidative_phosphorylation_deficiency|not_provided": 6,
    "not_provided|46_XX_gonadal_dysgenesis|Hypotonia_with_lactic_acidemia_and_hyperammonemia": 1,
    "not_specified|not_provided|MRPS22-related_disorder": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency|not_specified": 1,
    "not_provided|Microcephaly_19|_primary|_autosomal_recessive": 3,
    "COPB2-related_disorder|Osteoporosis|_childhood-_or_juvenile-onset|_with_developmental_delay": 2,
    "Osteoporosis|_childhood-_or_juvenile-onset|_with_developmental_delay": 5,
    "COPB2-related_disorder": 4,
    "Microcephaly_19|_primary|_autosomal_recessive": 1,
    "Osteoporosis|_childhood-_or_juvenile-onset|_with_developmental_delay|Microcephaly_19|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Osteoporosis|_childhood-_or_juvenile-onset|_with_developmental_delay|not_provided": 1,
    "Microcephaly_19|_primary|_autosomal_recessive|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_8": 2,
    "RASA2-related_disorder|not_specified": 2,
    "RASA2-related_disorder|not_specified|not_provided": 8,
    "not_provided|not_specified|RASA2-related_disorder": 1,
    "RASA2-related_disorder": 9,
    "RASA2-related_disorder|not_provided": 2,
    "RASA2-related_disorder|not_provided|not_specified": 3,
    "not_provided|RASA2-related_disorder|not_specified": 2,
    "not_specified|RASA2-related_disorder|not_provided": 2,
    "not_specified|not_provided|RASA2-related_disorder": 1,
    "not_specified|RASA2-related_disorder": 2,
    "Seckel_syndrome_1": 21,
    "Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided": 17,
    "Seckel_syndrome_1|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|not_provided": 2,
    "not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1": 16,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|not_provided|Seckel_syndrome_1": 6,
    "Seckel_syndrome_1|Inborn_genetic_diseases|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 11,
    "Inborn_genetic_diseases|Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 10,
    "not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|Inborn_genetic_diseases": 13,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|Inborn_genetic_diseases|not_provided": 9,
    "Inborn_genetic_diseases|not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 9,
    "not_provided|Seckel_syndrome_1|Inborn_genetic_diseases": 6,
    "not_provided|Seckel_syndrome_1": 16,
    "Inborn_genetic_diseases|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 24,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided|Inborn_genetic_diseases": 11,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1|Inborn_genetic_diseases": 14,
    "Seckel_syndrome_1|not_provided|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|ATR-related_disorder": 2,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 13,
    "not_provided|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|ATR-related_disorder|Seckel_syndrome_1": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 15,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|Seckel_syndrome_1|not_provided": 10,
    "ATR-related_disorder|Inborn_genetic_diseases|Seckel_syndrome_1|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 2,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases": 1,
    "Seckel_syndrome|Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|not_provided": 7,
    "Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified": 2,
    "not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|Seckel_syndrome_1": 10,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1": 2,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|not_provided|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|ATR-related_disorder|not_specified": 1,
    "Seckel_syndrome_1|not_provided": 7,
    "ATR-related_disorder|Seckel_syndrome_1|not_provided|not_specified": 1,
    "ATR-related_disorder": 5,
    "Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 5,
    "not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases": 12,
    "not_provided|Inborn_genetic_diseases|Seckel_syndrome_1": 4,
    "ATR-related_disorder|not_provided|Seckel_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 7,
    "Inborn_genetic_diseases|not_specified|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_specified|Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 2,
    "Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "Seckel_syndrome_1|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|ATR-related_disorder|not_provided": 1,
    "not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "ATR-related_disorder|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided": 3,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|ATR-related_disorder|Seckel_syndrome_1|not_provided": 1,
    "not_provided|ATR-related_disorder|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Seckel_syndrome_1": 2,
    "not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 8,
    "Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases": 10,
    "not_provided|Inborn_genetic_diseases|ATR-related_disorder|Seckel_syndrome_1": 2,
    "Seckel_syndrome_1|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 11,
    "not_provided|ATR-related_disorder|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 8,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|not_provided": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided": 4,
    "ATR-related_disorder|not_provided": 4,
    "ATR-related_disorder|not_specified|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1": 1,
    "not_provided|Seckel_syndrome|ATR-related_disorder": 1,
    "not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 4,
    "Seckel_syndrome_1|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 2,
    "not_provided|Seckel_syndrome_1|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 6,
    "not_provided|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 13,
    "Seckel_syndrome_1|Inborn_genetic_diseases|not_provided": 3,
    "Hereditary_cancer|not_specified|not_provided": 1,
    "not_provided|ATR-related_disorder|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_specified": 1,
    "not_provided|Seckel_syndrome": 2,
    "not_specified|not_provided|ATR-related_disorder|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_1": 3,
    "not_specified|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided": 1,
    "Seckel_syndrome_1|ATR-related_disorder|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Inborn_genetic_diseases|Seckel_syndrome_1": 3,
    "not_provided|ATR-related_disorder|Inborn_genetic_diseases": 1,
    "Seckel_syndrome_1|Cornelia_de_Lange_syndrome_1": 1,
    "ATR-related_disorder|Inborn_genetic_diseases|Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 11,
    "Seckel_syndrome_1|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 2,
    "not_provided|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 2,
    "Inborn_genetic_diseases|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1": 1,
    "ATR-related_disorder|not_specified|Seckel_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "ATR-related_disorder|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided": 2,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|ATR-related_disorder": 1,
    "not_provided|ATR-related_disorder|Seckel_syndrome_1|not_specified": 1,
    "not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 6,
    "not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified": 2,
    "not_provided|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "not_provided|Seckel_syndrome|Inborn_genetic_diseases": 1,
    "ATR-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "Seckel_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Seckel_syndrome_1|ATR-related_disorder": 1,
    "ATR-related_disorder|Inborn_genetic_diseases": 3,
    "Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|See_cases|not_provided": 1,
    "Seckel_syndrome|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|Seckel_syndrome_1": 1,
    "ATR-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 1,
    "not_provided|ATR-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|Seckel_syndrome_1|not_provided": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|Seckel_syndrome_1|not_provided": 1,
    "Seckel_syndrome_1|Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Seckel_syndrome_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1": 1,
    "Seckel_syndrome_1|Inborn_genetic_diseases": 2,
    "not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|ATR-X-related_syndrome|Seckel_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ATR-related_disorder": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|Seckel_syndrome_1": 1,
    "ATR-related_disorder|not_specified|not_provided|Seckel_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|ATR-related_disorder": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 2,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_specified|not_provided|ATR-related_disorder|Seckel_syndrome_1": 1,
    "Seckel_syndrome_1|Inborn_genetic_diseases|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_1|not_specified|not_provided": 2,
    "Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_specified|ATR-related_disorder": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Seckel_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Seckel_syndrome_1|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases": 1,
    "ATR-related_disorder|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1": 1,
    "Inborn_genetic_diseases|ATR-related_disorder|not_provided|Seckel_syndrome_1": 1,
    "not_specified|Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Seckel_syndrome_1|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|ATR-related_disorder|Inborn_genetic_diseases": 1,
    "ATR-related_disorder|not_provided|Malignant_tumor_of_breast|Seckel_syndrome_1": 1,
    "Seckel_syndrome_1|not_provided|Inborn_genetic_diseases": 2,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|not_provided|ATR-related_disorder": 1,
    "ATR-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|Familial_cancer_of_breast": 1,
    "Inborn_genetic_diseases|not_specified|ATR-related_disorder|not_provided|Seckel_syndrome_1|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Inborn_genetic_diseases|Seckel_syndrome": 1,
    "not_provided|Seckel_syndrome_1|ATR-related_disorder|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "Seckel_syndrome_1|Hereditary_cancer-predisposing_syndrome|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|not_provided": 1,
    "Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Seckel_syndrome_1|ATR-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Seckel_syndrome_1|Inborn_genetic_diseases|not_provided|not_specified|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome": 1,
    "not_provided|Familial_cutaneous_telangiectasia_and_oropharyngeal_predisposition_cancer_syndrome|Inborn_genetic_diseases|not_specified|Seckel_syndrome_1": 1,
    "not_specified|Seckel_syndrome": 1,
    "Seckel_syndrome": 2,
    "PLS1-related_disorder": 7,
    "not_provided|Hearing_loss|_autosomal_dominant_76|Autosomal_dominant_nonsyndromic_hearing_loss|Bilateral_sensorineural_hearing_impairment": 1,
    "Hearing_loss|_autosomal_dominant_76": 8,
    "PLS1-related_disorder|not_provided": 4,
    "Hearing_impairment|Hearing_loss|_autosomal_dominant_76": 1,
    "Hearing_loss|_autosomal_dominant_76|Hereditary_hearing_loss_and_deafness|Autosomal_dominant_nonsyndromic_hearing_loss": 1,
    "PLS1-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|PLS1-related_disorder": 1,
    "Inborn_genetic_diseases|PLS1-related_disorder": 2,
    "Inborn_genetic_diseases|PLS1-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_impairment|Hearing_impairment|Hearing_loss|_autosomal_dominant_76": 1,
    "Hearing_loss|_autosomal_dominant_76|not_provided": 2,
    "Autism|_susceptibility_to|_16": 6,
    "not_provided|SLC9A9-related_disorder": 4,
    "SLC9A9-related_disorder": 7,
    "not_specified|Autism|_susceptibility_to|_16|not_provided": 1,
    "not_specified|SLC9A9-related_disorder": 1,
    "SLC9A9-related_disorder|not_provided": 1,
    "Bruck_syndrome_2": 55,
    "Bruck_syndrome_2|not_provided": 18,
    "not_provided|Bruck_syndrome_2|Osteogenesis_imperfecta": 1,
    "not_provided|not_specified|PLOD2-related_disorder": 2,
    "not_specified|PLOD2-related_disorder": 1,
    "not_specified|Bruck_syndrome_2|Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Osteogenesis_imperfecta|Bruck_syndrome_2": 3,
    "Bruck_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Bruck_syndrome_2": 7,
    "Bruck_syndrome_2|Clubfoot|Femoral_bowing|Radial_bowing|Ulnar_bowing|Short_femur|Aplasia/hypoplasia_of_the_femur|Bowing_of_the_long_bones|Cleft_soft_palate|Camptodactyly|not_provided": 1,
    "PLOD2-related_disorder": 4,
    "Bruck_syndrome_2|Osteogenesis_imperfecta|not_provided": 1,
    "not_provided|Bruck_syndrome_2|not_specified": 1,
    "Bruck_syndrome_2|not_provided|Osteogenesis_imperfecta": 2,
    "PLOD2-related_disorder|not_provided": 2,
    "Osteogenesis_imperfecta|Bruck_syndrome_2|not_provided": 1,
    "not_provided|not_specified|Bruck_syndrome_2": 1,
    "Inborn_genetic_diseases|Bruck_syndrome_2|not_provided": 1,
    "not_specified|not_provided|Bruck_syndrome_2": 1,
    "not_specified|Osteogenesis_imperfecta|not_provided": 3,
    "not_provided|Bruck_syndrome_2|Clubfoot|Femoral_bowing|Radial_bowing|Ulnar_bowing|Short_femur|Aplasia/hypoplasia_of_the_femur|Bowing_of_the_long_bones|Cleft_soft_palate|Camptodactyly|not_specified": 1,
    "Osteogenesis_imperfecta|not_provided|Bruck_syndrome_2": 1,
    "not_provided|Osteogenesis_imperfecta|Bruck_syndrome_2|PLOD2-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Osteogenesis_imperfecta": 1,
    "PLOD2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "PLOD2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta": 3,
    "not_provided|Bruck_syndrome_2|Osteogenesis_imperfecta|PLOD2-related_disorder": 1,
    "PLOD2-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta|Bruck_syndrome_2": 1,
    "not_provided|PLOD2-related_disorder|not_specified|Osteogenesis_imperfecta|Bruck_syndrome_2": 1,
    "Bruck_syndrome_2|PLOD2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta": 4,
    "Bruck_syndrome_2|not_specified|not_provided": 1,
    "Bruck_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Bruck_syndrome_2|Osteogenesis_imperfecta|not_provided": 1,
    "ZIC1-related_disorder": 2,
    "not_provided|ZIC1-related_disorder": 4,
    "Structural_brain_anomalies_with_impaired_intellectual_development_and_craniosynostosis": 7,
    "ZIC1-related_disorder|not_provided": 2,
    "not_provided|not_specified|Craniosynostosis_6": 1,
    "Craniosynostosis_6": 2,
    "Structural_brain_anomalies_with_impaired_intellectual_development_and_craniosynostosis|not_provided": 1,
    "Inborn_genetic_diseases|ZIC1-related_disorder": 1,
    "AGTR1-related_disorder": 5,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic": 26,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|AGTR1-related_disorder": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|Renal_tubular_dysgenesis": 3,
    "Renal_tubular_dysgenesis|not_provided|AGTR1-related_disorder": 1,
    "Essential_hypertension|_genetic": 1,
    "AGTR1-related_disorder|not_provided|Renal_tubular_dysgenesis": 1,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|not_provided|Renal_tubular_dysgenesis": 2,
    "Renal_dysplasia|_cystic|_susceptibility_to|Anhydramnios": 2,
    "Inborn_genetic_diseases|Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|Renal_tubular_dysgenesis|not_provided": 2,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases": 1,
    "not_specified|Renal_tubular_dysgenesis|not_provided": 1,
    "Essential_hypertension|Renal_tubular_dysgenesis|not_provided": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis|not_provided": 2,
    "Inborn_genetic_diseases|Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|Inborn_genetic_diseases": 2,
    "Essential_hypertension|_genetic|Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases|not_provided": 2,
    "Renal_tubular_dysgenesis|not_specified|not_provided": 1,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|Retinitis_pigmentosa_40": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Essential_hypertension|_genetic|Renal_tubular_dysgenesis|not_provided|Hypertension|_essential|_susceptibility_to": 1,
    "CPB1-related_disorder": 7,
    "not_provided|CPB1-related_disorder": 2,
    "CPB1-related_disorder|not_provided": 3,
    "Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV": 73,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2": 105,
    "Inborn_genetic_diseases|Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|not_provided": 1,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|Inborn_genetic_diseases": 10,
    "GYG1-related_disorder|Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|not_provided": 1,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|not_provided": 5,
    "Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|GYG1-related_disorder|not_provided": 1,
    "not_specified|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|not_provided": 2,
    "not_specified|not_provided|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV": 1,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|not_specified": 2,
    "not_provided|not_specified|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV": 1,
    "Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|Inborn_genetic_diseases": 6,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|Inborn_genetic_diseases|not_provided": 1,
    "GYG1-related_disorder|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV": 2,
    "not_provided|Glycogen_storage_disease_XV": 1,
    "Inborn_genetic_diseases|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV": 2,
    "not_specified|Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2": 2,
    "GYG1-related_disorder|Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|not_specified|not_provided|Glycogen_storage_disease": 1,
    "not_provided|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|not_specified": 2,
    "Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|not_provided": 4,
    "not_provided|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV": 3,
    "GYG1-related_disorder|Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|Inborn_genetic_diseases|not_provided": 1,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|GYG1-related_disorder": 1,
    "GYG1-related_disorder": 1,
    "Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|not_specified": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2": 6,
    "Polyglucosan_body_myopathy_type_2": 2,
    "Glycogen_storage_disease_XV|Polyglucosan_body_myopathy_type_2|not_specified|Inborn_genetic_diseases": 1,
    "Polyglucosan_body_myopathy_type_2|Glycogen_storage_disease_XV|not_provided|GYG1-related_disorder|Inborn_genetic_diseases": 1,
    "HLTF-related_disorder": 20,
    "HLTF-related_disorder|not_specified": 3,
    "not_specified|HLTF-related_disorder": 1,
    "Familial_myelodysplastic_syndrome": 1,
    "Hermansky-Pudlak_syndrome_3": 116,
    "Hermansky-Pudlak_syndrome": 170,
    "not_provided|Hermansky-Pudlak_syndrome_3": 37,
    "Hermansky-Pudlak_syndrome|not_provided|Hermansky-Pudlak_syndrome_3": 1,
    "Hermansky-Pudlak_syndrome_3|not_provided": 41,
    "Hermansky-Pudlak_syndrome_3|not_provided|Hermansky-Pudlak_syndrome|not_specified": 1,
    "HPS3-related_disorder": 3,
    "not_provided|Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome": 6,
    "Hermansky-Pudlak_syndrome_3|not_provided|Inborn_genetic_diseases|HPS3-related_disorder": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_3": 1,
    "Hermansky-Pudlak_syndrome|not_provided": 44,
    "not_provided|Hermansky-Pudlak_syndrome": 41,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_3": 2,
    "Hermansky-Pudlak_syndrome_3|not_specified|not_provided": 1,
    "HPS3-related_disorder|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome_3|not_provided|HPS3-related_disorder": 1,
    "Inborn_genetic_diseases|HPS3-related_disorder|not_provided": 1,
    "Hermansky-Pudlak_syndrome_3|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3|not_provided": 4,
    "Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome|not_provided": 5,
    "not_provided|Hermansky-Pudlak_syndrome|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome_3|not_provided|Hermansky-Pudlak_syndrome": 2,
    "Hermansky-Pudlak_syndrome|not_provided|not_specified|Hermansky-Pudlak_syndrome_3": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3": 2,
    "Hermansky-Pudlak_syndrome_3|not_provided|HPS3-related_disorder|Hermansky-Pudlak_syndrome": 1,
    "not_provided|HPS3-related_disorder|Hermansky-Pudlak_syndrome": 2,
    "Hermansky-Pudlak_syndrome|not_specified|not_provided": 5,
    "HPS3-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome|not_provided|Hermansky-Pudlak_syndrome_3|not_specified": 1,
    "Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome|not_provided|not_specified": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3": 4,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_3|not_provided|Hermansky-Pudlak_syndrome": 1,
    "not_provided|Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome|HPS3-related_disorder|not_specified": 1,
    "HPS3-related_disorder|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3": 1,
    "not_provided|Hermansky-Pudlak_syndrome_3|not_specified": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_3": 2,
    "Hermansky-Pudlak_syndrome|HPS3-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3|HPS3-related_disorder": 2,
    "Hermansky-Pudlak_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Hermansky-Pudlak_syndrome_3|HPS3-related_disorder|Hermansky-Pudlak_syndrome": 1,
    "not_specified|Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome|not_provided": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3": 1,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_3|HPS3-related_disorder|not_provided|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_3|not_provided": 2,
    "Hermansky-Pudlak_syndrome_3|not_provided|Hermansky-Pudlak_syndrome|HPS3-related_disorder": 1,
    "Hermansky-Pudlak_syndrome_2|not_provided|Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome": 1,
    "not_specified|Hermansky-Pudlak_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3|not_provided": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_3|HPS3-related_disorder": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3|not_provided|not_specified": 1,
    "not_provided|HPS3-related_disorder|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_3": 2,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome": 1,
    "HPS3-related_disorder|not_provided": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome_3": 1,
    "Hermansky-Pudlak_syndrome|not_specified|not_provided|Deficiency_of_ferroxidase": 1,
    "Hermansky-Pudlak_syndrome_3|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_3|not_provided|Deficiency_of_ferroxidase": 1,
    "Deficiency_of_ferroxidase|not_provided|Hermansky-Pudlak_syndrome_3": 5,
    "Deficiency_of_ferroxidase|Hermansky-Pudlak_syndrome_3": 5,
    "Hermansky-Pudlak_syndrome_3|Deficiency_of_ferroxidase": 5,
    "Deficiency_of_ferroxidase|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_3|Deficiency_of_ferroxidase|Hermansky-Pudlak_syndrome": 1,
    "not_provided|Deficiency_of_ferroxidase|Hermansky-Pudlak_syndrome_3": 1,
    "Deficiency_of_ferroxidase|not_provided|Hermansky-Pudlak_syndrome": 1,
    "Deficiency_of_ferroxidase": 348,
    "not_specified|Deficiency_of_ferroxidase|not_provided|Hermansky-Pudlak_syndrome": 1,
    "not_provided|Deficiency_of_ferroxidase": 22,
    "CP-related_disorder": 6,
    "Deficiency_of_ferroxidase|not_provided": 18,
    "CP-related_disorder|Deficiency_of_ferroxidase": 6,
    "not_provided|Deficiency_of_ferroxidase|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|Deficiency_of_ferroxidase|Hermansky-Pudlak_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_ferroxidase": 3,
    "Deficiency_of_ferroxidase|CP-related_disorder": 3,
    "Neurodegeneration_with_brain_iron_accumulation|Deficiency_of_ferroxidase": 2,
    "Deficiency_of_ferroxidase|Inborn_genetic_diseases": 18,
    "not_provided|CP-related_disorder|Deficiency_of_ferroxidase|Hypoceruloplasminemia|not_specified": 1,
    "Inborn_genetic_diseases|Deficiency_of_ferroxidase": 19,
    "not_provided|Deficiency_of_ferroxidase|not_specified": 2,
    "CP-related_disorder|not_provided|Deficiency_of_ferroxidase|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Deficiency_of_ferroxidase": 9,
    "CP-related_disorder|not_specified|not_provided|Deficiency_of_ferroxidase": 2,
    "Deficiency_of_ferroxidase|not_specified": 3,
    "Deficiency_of_ferroxidase|.": 1,
    "not_provided|CP-related_disorder|Deficiency_of_ferroxidase|not_specified": 1,
    "CP-related_disorder|not_provided": 1,
    "Deficiency_of_ferroxidase|not_provided|Inborn_genetic_diseases": 1,
    "Deficiency_of_ferroxidase|not_provided|CP-related_disorder": 1,
    "not_specified|Deficiency_of_ferroxidase|not_provided": 2,
    "Deficiency_of_ferroxidase|not_provided|not_specified": 1,
    "Deficiency_of_ferroxidase|not_specified|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation|not_provided|Deficiency_of_ferroxidase|CP-related_disorder": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Deficiency_of_ferroxidase|not_provided": 1,
    "not_specified|Deficiency_of_ferroxidase": 5,
    "not_provided|not_specified|Deficiency_of_ferroxidase": 1,
    "not_provided|Deficiency_of_ferroxidase|CP-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Deficiency_of_ferroxidase|CP-related_disorder": 3,
    "not_provided|CP-related_disorder|Inborn_genetic_diseases|Deficiency_of_ferroxidase": 1,
    "CP-related_disorder|Inborn_genetic_diseases": 1,
    "CP-related_disorder|not_provided|Deficiency_of_ferroxidase": 1,
    "Deficiency_of_ferroxidase|Inborn_genetic_diseases|not_provided": 1,
    "Deficiency_of_ferroxidase|Neurodegeneration_with_brain_iron_accumulation|not_provided": 1,
    "Inborn_genetic_diseases|Deficiency_of_ferroxidase|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Deficiency_of_ferroxidase|Neurodegeneration_with_brain_iron_accumulation": 1,
    "Inborn_genetic_diseases|not_provided|CP-related_disorder|Deficiency_of_ferroxidase": 1,
    "Developmental_and_epileptic_encephalopathy|_73": 13,
    "RNF13-related_disorder": 3,
    "RNF13-related_disorder|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_73": 2,
    "Developmental_and_epileptic_encephalopathy|_73|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_73|not_specified|not_provided": 1,
    "EIF2A-related_disorder": 1,
    "Marinesco-Sj\u00f6gren_syndrome": 191,
    "Usher_syndrome_type_3": 40,
    "not_provided|Usher_syndrome_type_3": 19,
    "Usher_syndrome_type_3A|Usher_syndrome_type_3|not_provided": 1,
    "Usher_syndrome_type_3|not_provided": 8,
    "Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa-deafness_syndrome|not_provided": 5,
    "Retinitis_pigmentosa-deafness_syndrome|Retinitis_Pigmentosa|_Dominant": 1,
    "Usher_syndrome_type_3A": 26,
    "Retinal_dystrophy|Usher_syndrome_type_3|Inborn_genetic_diseases|not_provided": 1,
    "Usher_syndrome_type_3A|Usher_syndrome_type_3|not_provided|not_specified": 1,
    "Usher_syndrome_type_3A|not_provided|Retinitis_pigmentosa_61": 1,
    "Retinal_dystrophy|Usher_syndrome_type_3A|Retinitis_pigmentosa_61|not_provided|Usher_syndrome": 1,
    "Retinitis_pigmentosa_61": 9,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Retinitis_pigmentosa_61": 1,
    "not_provided|Retinitis_pigmentosa_61|Usher_syndrome_type_3A": 1,
    "Usher_syndrome_type_3A|Retinitis_pigmentosa_61": 3,
    "Retinitis_pigmentosa_61|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Usher_syndrome_type_3A|Usher_syndrome_type_3|Retinitis_pigmentosa_61": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_3A|not_provided": 2,
    "Retinitis_pigmentosa_61|Usher_syndrome_type_3A|Retinitis_pigmentosa|Usher_syndrome_type_3|Hearing_impairment|not_provided": 1,
    "Retinitis_pigmentosa_61|Usher_syndrome_type_3A|not_provided": 1,
    "Retinitis_pigmentosa_61|not_provided": 4,
    "Usher_syndrome_type_3A|not_provided|CLRN1-related_disorder|Usher_syndrome_type_3|Retinitis_pigmentosa_61|Retinal_dystrophy|Usher_syndrome": 1,
    "Retinitis_pigmentosa_61|Usher_syndrome_type_3": 3,
    "not_specified|CLRN1-related_disorder": 2,
    "Usher_syndrome_type_3A|not_specified|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|Usher_syndrome_type_3A|Hearing_impairment|Retinal_dystrophy|Optic_atrophy": 1,
    "Usher_syndrome_type_3A|not_provided": 7,
    "Retinitis_pigmentosa_61|not_provided|Usher_syndrome_type_3": 1,
    "Usher_syndrome_type_3|not_provided|Retinal_dystrophy|Usher_syndrome_type_3A|Retinitis_pigmentosa_61": 1,
    "Usher_syndrome_type_3A|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_61": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_3": 1,
    "Melnick-Fraser_syndrome|not_provided": 10,
    "not_provided|Usher_syndrome_type_3A|Retinitis_pigmentosa_61|Rare_genetic_deafness|Usher_syndrome_type_3|Usher_syndrome": 1,
    "not_provided|Usher_syndrome_type_3|not_specified": 1,
    "not_provided|Usher_syndrome_type_3A": 2,
    "Usher_syndrome_type_3|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_61|Retinitis_pigmentosa|Usher_syndrome_type_3A|not_provided": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_3|Retinitis_pigmentosa_61|Usher_syndrome_type_3A|Usher_syndrome": 1,
    "not_provided|Usher_syndrome_type_3A|Retinal_dystrophy": 1,
    "Usher_syndrome_type_3|Retinitis_pigmentosa_61": 1,
    "not_provided|CLRN1-related_disorder": 4,
    "CLRN1-related_disorder": 2,
    "Usher_syndrome_type_3A|Retinitis_pigmentosa_61|not_provided": 2,
    "not_provided|not_specified|Usher_syndrome_type_3": 1,
    "Retinitis_pigmentosa_61|Usher_syndrome_type_3A": 1,
    "not_provided|Usher_syndrome_type_3A|Retinitis_pigmentosa_61|Retinitis_pigmentosa|not_specified|Retinal_dystrophy": 1,
    "Neuronal_ceroid_lipofuscinosis|Retinitis_pigmentosa_61": 1,
    "not_provided|Retinitis_pigmentosa_61": 3,
    "Retinitis_pigmentosa_61|Usher_syndrome|Usher_syndrome_type_3A|not_provided": 1,
    "Retinitis_pigmentosa_61|Usher_syndrome_type_3A|Rare_genetic_deafness|Usher_syndrome_type_3|CLRN1-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "Usher_syndrome_type_3A|Usher_syndrome": 1,
    "CLRN1-related_disorder|Usher_syndrome_type_3A|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_3|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_3": 1,
    "Retinal_dystrophy|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_3|Retinitis_pigmentosa_61|Usher_syndrome_type_3A|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome|not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_61|Usher_syndrome_type_3A": 1,
    "Usher_syndrome_type_3A|Retinitis_pigmentosa|Retinitis_pigmentosa_61|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_3": 1,
    "Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_3": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_3A|Retinitis_pigmentosa_61": 1,
    "Usher_syndrome_type_3A|Retinitis_pigmentosa_61|CLRN1-related_disorder|Usher_syndrome|Retinal_dystrophy|not_provided|Usher_syndrome_type_3": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_61|not_provided": 1,
    "Usher_syndrome_type_3A|Usher_syndrome_type_3|Retinal_dystrophy|not_provided|not_specified": 1,
    "Usher_syndrome_type_3|Usher_syndrome_type_3A|Retinal_dystrophy|not_provided": 1,
    "Usher_syndrome_type_3A|not_provided|Retinal_dystrophy|not_specified": 1,
    "not_specified|not_provided|Usher_syndrome_type_3A|Usher_syndrome_type_3": 1,
    "Usher_syndrome_type_3A|Hearing_impairment": 1,
    "MED12L-related_disorder": 28,
    "Nizon-Isidor_syndrome|Inborn_genetic_diseases": 4,
    "Nizon-Isidor_syndrome": 57,
    "MED12L-related_disorder|Nizon-Isidor_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Nizon-Isidor_syndrome": 7,
    "not_specified|Inborn_genetic_diseases|MED12L-related_disorder": 1,
    "Inborn_genetic_diseases|Nizon-Isidor_syndrome": 2,
    "P2RY12-related_disorder|not_provided": 2,
    "Impaired_ADP-induced_platelet_aggregation|Platelet-type_bleeding_disorder_8": 1,
    "not_provided|Platelet-type_bleeding_disorder_8|not_specified": 2,
    "not_provided|Thrombocytopenia|Abnormal_bleeding|Platelet-type_bleeding_disorder_8": 1,
    "Platelet-type_bleeding_disorder_8": 4,
    "Impaired_ADP-induced_platelet_aggregation": 2,
    "P2RY12-related_disorder": 3,
    "Abnormal_platelet_function": 2,
    "not_provided|P2RY12-related_disorder": 1,
    "Platelet-type_bleeding_disorder_8|not_provided": 1,
    "Abnormal_bleeding|Thrombocytopenia|not_specified": 1,
    "not_provided|Platelet-type_bleeding_disorder_8": 1,
    "not_specified|Platelet-type_bleeding_disorder_8|not_provided": 1,
    "MED12L-related_neurodevelopmental_disorder": 2,
    "Nizon-Isidor_syndrome|not_provided": 2,
    "MED12L-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|MED12L-related_disorder": 2,
    "MED12L-associated_neurodevelopmental_disorder": 1,
    "Intellectual_disability|Nizon-Isidor_syndrome": 1,
    "MED12L-related_disorder|Inborn_genetic_diseases": 2,
    "Nizon-Isidor_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "MED12L-related_disorder|not_specified": 1,
    "not_provided|IGSF10-related_disorder|not_specified": 1,
    "IGSF10-related_disorder|not_provided": 26,
    "not_provided|IGSF10-related_disorder": 39,
    "not_specified|IGSF10-related_disorder|not_provided": 1,
    "IGSF10-related_disorder": 9,
    "Premature_ovarian_failure|not_provided": 3,
    "not_specified|not_provided|IGSF10-related_disorder": 1,
    "IGSF10-related_disorder|Premature_ovarian_failure|not_provided": 1,
    "IGSF10-related_disorder|not_specified|not_provided": 1,
    "Martsolf_syndrome_1|not_specified": 2,
    "MBNL1-related_disorder": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B14": 1,
    "DHX36-associated_disorder": 1,
    "not_provided|MME-related_disorder": 2,
    "MME-related_disorder|not_provided": 4,
    "not_provided|Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_axonal_type_2T|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|not_provided": 14,
    "Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_axonal_type_2T|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|Spinocerebellar_ataxia_43": 1,
    "MME-related_autosomal_dominant_Charcot_Marie_Tooth_disease_type_2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2T": 7,
    "MME-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2T|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_axonal_type_2T": 2,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2T|Inborn_genetic_diseases": 2,
    "Spinocerebellar_ataxia_43": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_type_2T|not_provided|See_cases": 1,
    "Distal_myopathy|Peripheral_neuropathy": 1,
    "not_provided|Autosomal_recessive_axonal_hereditary_motor_and_sensory_neuropathy": 1,
    "MME-related_disorder": 2,
    "Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_axonal_type_2T|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Spinocerebellar_ataxia_43": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2T": 1,
    "not_provided|Peripheral_neuropathy": 10,
    "Early-onset_dementia_of_unclear_type|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2T|Spinocerebellar_ataxia_43": 1,
    "Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_axonal_type_2T": 2,
    "Spinocerebellar_ataxia_43|MME-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2T|not_provided|Congenital_membranous_nephropathy_due_to_maternal_anti-neutral_endopeptidase_alloimmunization": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2T": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|Spinocerebellar_ataxia_43|Inborn_genetic_diseases|not_provided": 1,
    "MME-related_autosomal_dominant_Charcot_Marie_Tooth_disease_type_2|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|not_provided|MME-related_disorder": 1,
    "not_provided|Spinocerebellar_ataxia_43": 2,
    "Spinocerebellar_ataxia_43|not_provided": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2T|Charcot-Marie-Tooth_disease_type_2|MME-related_autosomal_dominant_Charcot_Marie_Tooth_disease_type_2|Spinocerebellar_ataxia_43|not_provided": 1,
    "Peripheral_neuropathy|Charcot-Marie-Tooth_disease_axonal_type_2T": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2T": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2T": 1,
    "MME-related_distal_hereditary_motor_neuropathies": 1,
    "MME-related_disorder|not_provided|Spinocerebellar_ataxia_43|Charcot-Marie-Tooth_disease_axonal_type_2T": 1,
    "Holoprosencephaly_14": 2,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia": 6,
    "Hereditary_spastic_paraplegia_42|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_42|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided": 4,
    "Inborn_genetic_diseases|Spastic_paraplegia|Huppke-Brendel_syndrome|Hereditary_spastic_paraplegia_42|not_provided": 1,
    "Huppke-Brendel_syndrome": 5,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 10,
    "Hereditary_spastic_paraplegia_42|Huppke-Brendel_syndrome|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_42|Inborn_genetic_diseases": 1,
    "SLC33A1-related_disorder": 6,
    "Huppke-Brendel_syndrome|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided": 48,
    "Failure_to_thrive|Global_developmental_delay|Hypothyroidism": 1,
    "Huppke-Brendel_syndrome|Hereditary_spastic_paraplegia_42": 1,
    "not_provided|Spastic_paraplegia|not_specified": 9,
    "SLC33A1-related_hereditary_spastic_paraplegia": 1,
    "SLC33A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Spastic_paraplegia|not_provided|Huppke-Brendel_syndrome|Hereditary_spastic_paraplegia_42": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_provided": 21,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_42": 3,
    "not_provided|Huppke-Brendel_syndrome": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|not_provided": 1,
    "not_provided|Spastic_paraplegia|SLC33A1-related_disorder": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|SLC33A1-related_disorder|Spastic_paraplegia": 1,
    "PTX3-related_disorder": 3,
    "not_specified|PTX3-related_disorder": 2,
    "not_provided|PTX3-related_disorder": 1,
    "not_specified|Congenital_long_QT_syndrome": 2,
    "SHOX2-related_disorder": 4,
    "SHOX2-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_70": 9,
    "RSRC1-related_disorder|not_provided": 1,
    "not_provided|Autism": 6,
    "Intellectual_developmental_disorder|_autosomal_recessive_70|Inborn_genetic_diseases": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_70|not_provided": 1,
    "RSRC1-related_disorder": 1,
    "MLF1-related_disorder": 4,
    "MLF1-related_disorder|not_provided": 1,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_provided": 56,
    "GFM1-related_disorder|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_specified": 1,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_provided|not_specified": 3,
    "not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 52,
    "not_specified|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_provided": 6,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|GFM1-related_disorder|not_provided": 2,
    "not_provided|not_specified|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 5,
    "GFM1-related_disorder|not_provided": 6,
    "not_specified|not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 4,
    "GFM1-related_disorder|not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 3,
    "Inborn_genetic_diseases|not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Inborn_genetic_diseases": 2,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Leigh_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "GFM1-related_disorder|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_provided": 1,
    "not_provided|GFM1-related_disorder|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 2,
    "GFM1-related_disorder": 6,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_provided|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|See_cases": 1,
    "not_provided|Severe_muscular_hypotonia|Relative_macrocephaly|Developmental_regression|not_specified": 1,
    "not_specified|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "not_provided|not_specified|GFM1-related_disorder|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "Inborn_genetic_diseases|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_provided": 1,
    "not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|GFM1-related_disorder": 1,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Inborn_genetic_diseases": 3,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_specified": 1,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Inborn_genetic_diseases|not_provided": 2,
    "Combined_oxidative_phosphorylation_deficiency|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|See_cases": 1,
    "See_cases|not_provided|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "not_provided|GFM1-related_disorder|not_specified|Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1": 1,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|not_specified|not_provided": 1,
    "GFM1-related_disorder|not_specified|not_provided": 1,
    "not_provided|GFM1-related_disorder": 1,
    "Combined_oxidative_phosphorylation_deficiency": 30,
    "Familial_meningioma": 419,
    "Asphyxiating_thoracic_dystrophy_2": 83,
    "not_provided|Asphyxiating_thoracic_dystrophy_2": 2,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2": 21,
    "Asphyxiating_thoracic_dystrophy_2|Jeune_thoracic_dystrophy": 25,
    "IFT80-related_disorder|Jeune_thoracic_dystrophy": 2,
    "not_specified|Jeune_thoracic_dystrophy": 8,
    "not_specified|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2": 1,
    "Asphyxiating_thoracic_dystrophy_2|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 11,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_2": 1,
    "Asphyxiating_thoracic_dystrophy_2|not_provided|Jeune_thoracic_dystrophy|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 5,
    "IFT80-related_disorder|Asphyxiating_thoracic_dystrophy_2|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_2": 2,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases": 48,
    "Jeune_thoracic_dystrophy|IFT80-related_disorder": 1,
    "IFT80-related_disorder": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_2|Jeune_thoracic_dystrophy": 2,
    "not_provided|not_specified|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2": 2,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2|not_provided": 4,
    "Asphyxiating_thoracic_dystrophy_2|Jeune_thoracic_dystrophy|not_provided": 2,
    "Asphyxiating_thoracic_dystrophy_2|not_provided|not_specified|Jeune_thoracic_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_2|IFT80-related_disorder|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_2": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_2|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_2|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2|Inborn_genetic_diseases": 5,
    "Asphyxiating_thoracic_dystrophy_2|not_provided": 2,
    "Asphyxiating_thoracic_dystrophy_2|Inborn_genetic_diseases": 6,
    "Asphyxiating_thoracic_dystrophy_2|Inborn_genetic_diseases|Connective_tissue_disorder|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 52,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2|not_provided|IFT80-related_disorder|Type_IV_short_rib_polydactyly_syndrome": 1,
    "not_specified|Jeune_thoracic_dystrophy|Connective_tissue_disorder": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_2|Connective_tissue_disorder|not_specified|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|not_specified|Connective_tissue_disorder": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2|not_specified": 1,
    "Asphyxiating_thoracic_dystrophy_2|not_specified|Jeune_thoracic_dystrophy|not_provided": 1,
    "Jeune_thoracic_dystrophy|not_provided|IFT80-related_disorder|Asphyxiating_thoracic_dystrophy_2": 1,
    "Asphyxiating_thoracic_dystrophy_2|Jeune_thoracic_dystrophy|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|IFT80-related_disorder|Asphyxiating_thoracic_dystrophy_2|Jeune_thoracic_dystrophy": 2,
    "IFT80-related_disorder|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_2": 2,
    "not_provided|Asphyxiating_thoracic_dystrophy_2|Connective_tissue_disorder|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|Jeune_thoracic_dystrophy": 1,
    "Type_IV_short_rib_polydactyly_syndrome": 2,
    "not_provided|Connective_tissue_disorder|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_2": 1,
    "Asphyxiating_thoracic_dystrophy_2|not_provided|Jeune_thoracic_dystrophy": 1,
    "not_specified|Jeune_thoracic_dystrophy|Connective_tissue_disorder|not_provided|Asphyxiating_thoracic_dystrophy_2": 1,
    "Jeune_thoracic_dystrophy|Short-rib_thoracic_dysplasia_10_with_or_without_polydactyly": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Connective_tissue_disorder": 1,
    "not_specified|Bone_marrow_failure_syndrome": 1,
    "Bone_marrow_failure_syndrome": 1,
    "KPNA4-related_condition": 1,
    "p_phenotype": 9,
    "B3GALNT1-related_disorder": 7,
    "Sucrase-isomaltase_deficiency": 197,
    "not_provided|Sucrase-isomaltase_deficiency": 107,
    "SI-related_disorder|not_provided": 4,
    "Sucrase-isomaltase_deficiency|not_specified|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|Sucrase-isomaltase_deficiency": 11,
    "Inborn_genetic_diseases|Sucrase-isomaltase_deficiency": 4,
    "Sucrase-isomaltase_deficiency|not_provided": 127,
    "not_provided|Sucrase-isomaltase_deficiency|SI-related_disorder": 5,
    "not_provided|Sucrase-isomaltase_deficiency|Inborn_genetic_diseases": 5,
    "Sucrase-isomaltase_deficiency|Inborn_genetic_diseases|not_provided": 5,
    "SI-related_disorder|not_provided|Sucrase-isomaltase_deficiency": 4,
    "SI-related_disorder": 9,
    "not_provided|Sucrase-isomaltase_deficiency|not_specified": 3,
    "not_provided|SI-related_disorder|Inborn_genetic_diseases": 1,
    "Sucrase-isomaltase_deficiency|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|not_provided|SI-related_disorder": 3,
    "Inborn_genetic_diseases|Sucrase-isomaltase_deficiency|not_provided": 14,
    "not_provided|SI-related_disorder": 2,
    "not_provided|not_specified|Sucrase-isomaltase_deficiency": 1,
    "Sucrase-isomaltase_deficiency|not_provided|SI-related_disorder": 7,
    "SI-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Sucrase-isomaltase_deficiency": 2,
    "SI-related_disorder|Sucrase-isomaltase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Sucrase-isomaltase_deficiency|SI-related_disorder|not_provided": 3,
    "Congenital_sucrose-isomaltase_deficiency|Sucrase-isomaltase_deficiency|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Sucrase-isomaltase_deficiency": 1,
    "Sucrase-isomaltase_deficiency|SI-related_disorder": 1,
    "SI-related_disorder|Sucrase-isomaltase_deficiency|not_provided": 1,
    "not_provided|SI-related_disorder|Sucrase-isomaltase_deficiency": 1,
    "Sucrase-isomaltase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Sucrase-isomaltase_deficiency|SI-related_disorder": 1,
    "Deficiency_of_butyrylcholinesterase": 86,
    "not_provided|Deficiency_of_butyrylcholinesterase": 11,
    "Inborn_genetic_diseases|Deficiency_of_butyrylcholinesterase": 2,
    "not_specified|not_provided|Deficiency_of_butyrylcholinesterase|Butyrylcholinesterase_activity": 1,
    "Deficiency_of_butyrylcholinesterase|not_specified": 4,
    "BCHE|_J_variant|not_specified": 1,
    "Deficiency_of_butyrylcholinesterase|BCHE-related_disorder": 3,
    "Pseudocholinesterase_deficiency|Inborn_genetic_diseases": 1,
    "Deficiency_of_butyrylcholinesterase|BCHE|_fluoride_2|BCHE-related_disorder": 1,
    "Deficiency_of_butyrylcholinesterase|Butyrylcholinesterase_deficiency|_fluoride-resistant|_Japanese_type": 1,
    "not_specified|Deficiency_of_butyrylcholinesterase": 2,
    "not_provided|Deficiency_of_butyrylcholinesterase|BCHE|_flouride_1": 1,
    "BCHE-related_disorder": 2,
    "not_specified|not_provided|Deficiency_of_butyrylcholinesterase|See_cases": 1,
    "BCHE-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|BCHE|_H_variant": 1,
    "Deficiency_of_butyrylcholinesterase|not_provided": 3,
    "BCHE-related_disorder|not_specified|not_provided|Deficiency_of_butyrylcholinesterase": 1,
    "Inborn_genetic_diseases|BCHE-related_disorder": 1,
    "BCHE-related_disorder|not_provided|Postanesthetic_apnea|Deficiency_of_butyrylcholinesterase": 1,
    "Suxamethonium_response_-_slow_metabolism": 1,
    "not_provided|Cerebral_cavernous_malformation_3": 4,
    "Cerebral_cavernous_malformation_3": 96,
    "Cerebral_cavernous_malformation_3|not_provided": 5,
    "Inborn_genetic_diseases|Cerebral_cavernous_malformation_3": 4,
    "Cerebral_cavernous_malformation_3|Cerebral_cavernous_malformation": 1,
    "Cerebral_cavernous_malformation|Cerebral_cavernous_malformation_3|PDCD10-related_disorder": 1,
    "Cerebral_arteriovenous_malformation|Seizure|Hemiparesis|Cavernous_hemangioma|Hereditary_cavernous_hemangioma_of_brain|PDCD10-related_disorder|Cerebral_cavernous_malformation_3|not_provided": 1,
    "PDCD10-related_disorder": 2,
    "Cerebral_cavernous_malformation|Cerebral_cavernous_malformation_3": 1,
    "Cerebral_cavernous_malformation_3|Inborn_genetic_diseases": 2,
    "not_provided|Cerebral_cavernous_malformation_3|PDCD10-related_disorder": 1,
    "Cerebral_cavernous_malformation_3|PDCD10-related_disorder|not_provided": 1,
    "Cerebral_cavernous_malformation_3|PDCD10-related_disorder": 1,
    "Cerebral_cavernous_malformation_1": 5,
    "Cerebral_cavernous_malformation_3|not_specified|not_provided": 1,
    "not_provided|Cerebral_cavernous_malformation|Cerebral_cavernous_malformation_3": 1,
    "not_specified|Cerebral_cavernous_malformation_3": 1,
    "Cerebral_cavernous_malformation|Familial_encephalopathy_with_neuroserpin_inclusion_bodies|SERPINI1-related_disorder": 1,
    "not_provided|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 8,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 287,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|Cerebral_cavernous_malformation_3|not_provided": 1,
    "not_provided|Cerebral_cavernous_malformation|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 1,
    "not_provided|not_specified|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 3,
    "not_provided|SERPINI1-related_disorder|not_specified|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 11,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|SERPINI1-related_disorder|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|SERPINI1-related_disorder|not_provided": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|Inborn_genetic_diseases|not_specified": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|SERPINI1-related_disorder": 2,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|not_provided": 5,
    "SERPINI1-related_disorder|Familial_encephalopathy_with_neuroserpin_inclusion_bodies|not_provided": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|SERPINI1-related_disorder|Inborn_genetic_diseases": 1,
    "SERPINI1-related_disorder|not_provided|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 1,
    "Inborn_genetic_diseases|SERPINI1-related_disorder": 1,
    "not_specified|Familial_encephalopathy_with_neuroserpin_inclusion_bodies": 2,
    "not_specified|not_provided|Familial_encephalopathy_with_neuroserpin_inclusion_bodies|SERPINI1-related_disorder": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|not_specified": 1,
    "Familial_encephalopathy_with_neuroserpin_inclusion_bodies|Abnormality_of_the_nervous_system": 1,
    "MECOM-related_disorder": 11,
    "not_provided|MECOM-related_disorder": 5,
    "MECOM-related_disorder|Inborn_genetic_diseases|not_provided": 5,
    "Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2": 23,
    "not_specified|Inborn_genetic_diseases|MECOM-related_disorder|not_provided": 1,
    "not_provided|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2": 2,
    "Radioulnar_synostosis": 44,
    "Radioulnar_synostosis|not_provided": 4,
    "MECOM-related_disorder|Inborn_genetic_diseases": 6,
    "MECOM-associated_syndrome|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2|MECOM-related_disorder|not_provided": 1,
    "not_specified|MECOM-related_disorder|not_provided": 1,
    "Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|MECOM-related_disorder": 1,
    "MECOM-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2": 1,
    "not_provided|Inborn_genetic_diseases|MECOM-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|MECOM-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2": 3,
    "MECOM-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MECOM-related_disorder": 4,
    "MECOM-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "MECOM-related_disorder|not_specified|not_provided": 1,
    "Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_1": 7,
    "not_provided|MECOM-related_disorder|Inborn_genetic_diseases": 1,
    "MECOM-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Thrombocytopenia|Abnormal_bleeding|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2": 2,
    "not_specified|MECOM-related_disorder": 1,
    "Malignant_peritoneal_mesothelioma": 3,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_1|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Aplastic_anemia": 1,
    "TERC-related_disorder": 3,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2": 3,
    "Aplastic_anemia": 86,
    "Dyskeratosis_congenita|_autosomal_dominant_1|not_provided|TERC-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|not_provided": 5,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_1": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2": 5,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|Dyskeratosis_congenita|_autosomal_dominant_1": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_1": 8,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "TERC-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|TERC-related_disorder|Pulmonary_fibrosis": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1|TERC-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|not_provided|Pulmonary_fibrosis": 1,
    "Aplastic_anemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|TERC-related_disorder": 1,
    "TERC-related_disorder|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|Interstitial_lung_disease_2": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|Dyskeratosis_congenita|_autosomal_dominant_1|Telomere_syndrome": 1,
    "Aplastic_anemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Aplastic_anemia|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|not_specified|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2|Pulmonary_fibrosis": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_2": 1,
    "TERC-related_disorder|not_specified": 1,
    "TERC-related_disorder|not_specified|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Paroxysmal_nocturnal_hemoglobinuria_1": 9,
    "not_specified|not_provided|TERC-related_disorder": 1,
    "Macular_dystrophy_with_or_without_cone_dysfunction": 2,
    "MACULAR_DYSTROPHY_WITH_CONE_DYSFUNCTION": 3,
    "GPR160-related_disorder": 2,
    "PRKCI-related_disorder": 3,
    "Leukodystrophy|_hypomyelinating|_22": 4,
    "not_provided|SLC7A14-related_disorder": 5,
    "not_provided|Retinitis_pigmentosa_68": 3,
    "Retinitis_pigmentosa_68": 3,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_68": 1,
    "Retinitis_pigmentosa_68|Retinal_dystrophy|not_provided|SLC7A14-related_disorder": 1,
    "Retinitis_pigmentosa_68|Retinal_dystrophy|not_provided": 2,
    "Optic_atrophy|Retinal_dystrophy|not_specified|Retinitis_pigmentosa_68|not_provided": 1,
    "not_provided|SLC7A14-related_disorder|not_specified": 1,
    "SLC7A14-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_68|not_provided|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_68|SLC7A14-related_disorder|Retinal_dystrophy": 1,
    "Fanconi-Bickel_syndrome": 177,
    "Fanconi-Bickel_syndrome|not_provided": 3,
    "not_provided|Fanconi-Bickel_syndrome": 6,
    "Fanconi-Bickel_syndrome|not_specified": 4,
    "Inborn_genetic_diseases|Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus": 4,
    "Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus": 36,
    "Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus|Inborn_genetic_diseases": 1,
    "Fanconi-Bickel_syndrome|Monogenic_diabetes": 1,
    "SLC2A2-related_disorder|Fanconi-Bickel_syndrome": 2,
    "Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome": 7,
    "not_provided|not_specified|Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus": 1,
    "SLC2A2-related_disorder|Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|not_provided": 1,
    "Fanconi-Bickel_syndrome|SLC2A2-related_disorder": 3,
    "Fanconi-Bickel_syndrome|SLC2A2-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Fanconi-Bickel_syndrome|SLC2A2-related_disorder": 1,
    "not_specified|SLC2A2-related_disorder|Fanconi-Bickel_syndrome": 1,
    "Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|Congenital_long_QT_syndrome|not_provided": 1,
    "Fanconi-Bickel_syndrome|not_provided|SLC2A2-related_disorder": 1,
    "not_specified|Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus": 1,
    "Fanconi-Bickel_syndrome|not_provided|not_specified": 1,
    "Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|Inborn_genetic_diseases": 1,
    "SLC2A2-related_disorder": 6,
    "Inborn_genetic_diseases|Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome": 1,
    "Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|not_provided": 3,
    "Fanconi-Bickel_syndrome|Inborn_genetic_diseases": 3,
    "Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus|not_specified": 2,
    "not_specified|Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus|not_provided": 1,
    "Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi-Bickel_syndrome": 3,
    "not_provided|Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome": 1,
    "not_specified|Fanconi-Bickel_syndrome|not_provided|SLC2A2-related_disorder": 1,
    "not_specified|not_provided|Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus": 1,
    "Monogenic_diabetes|Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|Diabetes_mellitus_type_2|_susceptibility_to": 1,
    "not_specified|Fanconi-Bickel_syndrome|not_provided": 3,
    "Fanconi-Bickel_syndrome|Type_2_diabetes_mellitus|SLC2A2-related_disorder": 1,
    "Fanconi-Bickel_syndrome|SLC2A2-related_disorder|not_provided": 1,
    "not_specified|Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome": 1,
    "not_specified|Fanconi-Bickel_syndrome|SLC2A2-related_disorder": 1,
    "Fanconi-Bickel_syndrome|not_provided|Monogenic_diabetes|not_specified": 1,
    "Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|not_specified": 2,
    "not_provided|not_specified|Fanconi-Bickel_syndrome|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome|SLC2A2-related_disorder": 1,
    "SLC2A2-related_disorder|Type_2_diabetes_mellitus|Fanconi-Bickel_syndrome": 1,
    "TNIK-related_disorder": 9,
    "TNIK-related_disorder|not_provided": 3,
    "TNIK-related_disorder|Intellectual_disability|_autosomal_recessive_54|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_54": 6,
    "Intellectual_disability|_autosomal_recessive_54": 3,
    "not_specified|Intellectual_disability|_autosomal_recessive_54": 1,
    "Intellectual_disability|_autosomal_recessive_54|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_54|not_provided": 2,
    "not_provided|TNIK-related_disorder": 1,
    "not_provided|Cardiac_valvular_defect|_developmental": 6,
    "not_provided|PLD1-related_disorder": 8,
    "Cardiac_valvular_defect|_developmental": 20,
    "Inborn_genetic_diseases|PLD1-related_disorder|not_provided": 1,
    "Cardiac_valvular_defect|_developmental|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Cardiac_valvular_defect|_developmental": 1,
    "PLD1-related_disorder|not_provided": 7,
    "PLD1-related_disorder": 5,
    "Cardiac_valvular_defect|_developmental|Inborn_genetic_diseases": 2,
    "FNDC3B-related_disorder": 8,
    "FNDC3B-related_disorder|not_provided": 2,
    "not_provided|FNDC3B-related_disorder": 2,
    "Short_stature_due_to_partial_GHR_deficiency": 6,
    "Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency": 50,
    "Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|not_provided": 3,
    "not_provided|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency": 12,
    "not_specified|not_provided|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|GHSR-related_disorder": 1,
    "Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|not_specified|not_provided": 1,
    "Pseudohypoparathyroidism_type_1B": 145,
    "not_provided|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency": 1,
    "Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|Inborn_genetic_diseases|not_provided|Short_stature": 1,
    "GHSR-related_disorder": 3,
    "not_specified|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency": 1,
    "not_specified|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|not_provided": 1,
    "not_specified|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency": 1,
    "Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|not_provided|not_specified": 1,
    "GHSR-related_disorder|not_provided": 1,
    "Globozoospermia": 31,
    "SPATA16-related_disorder|not_provided": 2,
    "Globozoospermia|not_provided": 8,
    "Globozoospermia|SPATA16-related_disorder|not_provided": 1,
    "Spermatogenic_Failure": 7,
    "not_provided|Globozoospermia": 5,
    "Globozoospermia|SPATA16-related_disorder": 1,
    "Globozoospermia|not_specified": 2,
    "not_specified|Globozoospermia": 1,
    "NLGN1-related_disorder": 12,
    "Autism|_susceptibility_to|_20": 6,
    "Inborn_genetic_diseases|Autism|_susceptibility_to|_20": 1,
    "Intellectual_disability|_X-linked_102": 142,
    "Inborn_genetic_diseases|NLGN1-related_disorder": 2,
    "NLGN1-related_disorder|not_provided": 2,
    "not_specified|NAALADL2-related_disorder": 1,
    "NAALADL2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Pierpont_syndrome": 2,
    "Pierpont_syndrome": 315,
    "Pierpont_syndrome|not_specified|not_provided": 1,
    "Pierpont_syndrome|Inborn_genetic_diseases": 9,
    "TBL1XR1-related_disorder|Intellectual_disability|_autosomal_dominant_41": 1,
    "Intellectual_disability|_autosomal_dominant_41": 28,
    "not_provided|Inborn_genetic_diseases|Pierpont_syndrome": 2,
    "Pierpont_syndrome|not_provided": 20,
    "not_provided|Pierpont_syndrome": 21,
    "Intellectual_disability|_autosomal_dominant_41|Pierpont_syndrome|not_provided": 1,
    "TBL1XR1-related_disorder|Malignant_lymphoma|_large_B-cell|_diffuse|Pierpont_syndrome|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_41|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_41|Pierpont_syndrome": 9,
    "Pierpont_syndrome|Intellectual_disability|_autosomal_dominant_41|not_provided|Intellectual_disability": 1,
    "not_specified|Pierpont_syndrome": 3,
    "Pierpont_syndrome|Intellectual_disability|_autosomal_dominant_41": 6,
    "Conotruncal_heart_malformations": 75,
    "Malignant_lymphoma|_large_B-cell|_diffuse": 10,
    "Intellectual_disability|_autosomal_dominant_41|TBL1XR1-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_41|Pierpont_syndrome|not_provided|Intellectual_disability": 1,
    "TBL1XR1-related_disorder|Pierpont_syndrome": 3,
    "TBL1XR1-related_neurodevelopmental_disorder": 2,
    "See_cases|Intellectual_disability|_autosomal_dominant_41": 1,
    "Pierpont_syndrome|Intellectual_disability|_autosomal_dominant_41|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_41|Pierpont_syndrome": 2,
    "Cleft_lip/palate|Pierpont_syndrome|not_specified": 1,
    "TBL1XR1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Pierpont_syndrome": 3,
    "not_provided|TBL1XR1-related_disorder": 2,
    "not_provided|Pierpont_syndrome|Inborn_genetic_diseases": 5,
    "TBL1XR1-related_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_41": 1,
    "TBL1XR1-related_disorder": 3,
    "not_provided|Pierpont_syndrome|Intellectual_disability|_autosomal_dominant_41": 1,
    "Pierpont_syndrome|Intellectual_disability|_autosomal_dominant_41|Inborn_genetic_diseases|not_provided": 2,
    "Pierpont_syndrome|not_provided|TBL1XR1-related_disorder|not_specified|Intellectual_disability|_autosomal_dominant_41|Inborn_genetic_diseases": 1,
    "Pierpont_syndrome|TBL1XR1-related_disorder|not_provided": 1,
    "TBL1XR1-related_disorder|not_specified": 1,
    "Pierpont_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_41|Pierpont_syndrome|Inborn_genetic_diseases|not_specified|not_provided|TBL1XR1-related_disorder": 1,
    "Pierpont_syndrome|not_specified": 1,
    "Pierpont_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_41": 1,
    "Pierpont_syndrome|TBL1XR1-related_disorder": 3,
    "Pierpont_syndrome|TBL1XR1-related_disorder|Inborn_genetic_diseases": 1,
    "Pierpont_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "TBL1XR1-related_neurodevelopmental_disorders|_including_Pierpont_syndrome|not_specified": 1,
    "Cowden_syndrome_1": 290,
    "Cowden_syndrome|Epidermal_nevus|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|not_provided": 1,
    "Cowden_syndrome_5": 7,
    "Inborn_genetic_diseases|Cowden_syndrome": 95,
    "Cowden_syndrome": 328,
    "Cowden_syndrome|Inborn_genetic_diseases": 74,
    "Cowden_syndrome|not_provided": 8,
    "PIK3CA_related_overgrowth_syndrome": 14,
    "Cowden_syndrome|Cowden_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Cowden_syndrome|not_specified": 1,
    "PIK3CA-related_disorder|Cowden_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|CLOVES_syndrome|Abnormal_cardiovascular_system_morphology": 1,
    "CLAPO_syndrome": 1,
    "Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|Cowden_syndrome_5|Ovarian_neoplasm|CLOVES_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Abnormal_cerebral_morphology": 1,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|PIK3CA_related_overgrowth_syndrome|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|PIK3CA-related_disorder|not_provided": 1,
    "Global_developmental_delay|Hypospadias|Macrocephaly|not_provided|Cowden_syndrome_5": 1,
    "Cerebral_cavernous_malformation_4": 1,
    "PIK3CA-related_disorder|PIK3CA_related_overgrowth_syndrome|not_provided|Cowden_syndrome": 1,
    "Familial_cancer_of_breast|Cowden_syndrome_5|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Seborrheic_keratosis|Hemifacial_myohyperplasia|Epidermal_nevus|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Ovarian_cancer|Cerebral_cavernous_malformation_4|Lung_cancer|CLAPO_syndrome|CLOVES_syndrome|Inborn_genetic_diseases": 1,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 9,
    "Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|CLOVES_syndrome": 1,
    "Cowden_syndrome|not_specified|Inborn_genetic_diseases|not_provided|Cowden_syndrome_5": 1,
    "PIK3CA_related_overgrowth_syndrome|Cowden_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_1": 65,
    "Cowden_syndrome|not_specified|not_provided|See_cases|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "PIK3CA-related_disorder|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Inborn_genetic_diseases|Angioosteohypertrophic_syndrome|CLOVES_syndrome|Rare_venous_malformation|PIK3CA_related_overgrowth_syndrome|not_provided": 1,
    "Cowden_syndrome_5|PIK3CA_related_overgrowth_syndrome": 1,
    "PIK3CA-related_disorder": 10,
    "Cowden_syndrome|Gastric_cancer|CLAPO_syndrome|CLOVES_syndrome|Cerebral_cavernous_malformation_4|Cowden_syndrome_5|Familial_cancer_of_breast|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Seborrheic_keratosis|Hepatocellular_carcinoma|Colorectal_cancer|Hemifacial_myohyperplasia|Congenital_macrodactylia|Epidermal_nevus|Ovarian_cancer|Lung_cancer|not_provided": 1,
    "PIK3CA-related_disorder|MACRODACTYLY|_SOMATIC|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|CLAPO_syndrome|PIK3CA_related_overgrowth_syndrome": 1,
    "Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided": 1,
    "not_provided|Cowden_syndrome": 6,
    "PIK3CA_related_overgrowth_syndrome|Cowden_syndrome|Angioosteohypertrophic_syndrome|not_provided|Cowden_syndrome_5|Keratoacanthoma": 1,
    "PIK3CA-related_disorder|not_provided|Cowden_syndrome|not_specified|Cowden_syndrome_5|Inborn_genetic_diseases": 1,
    "Familial_cancer_of_breast|PIK3CA_related_overgrowth_syndrome": 1,
    "Cowden_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Carcinoma_of_colon|Familial_cancer_of_breast|CLOVES_syndrome|Cowden_syndrome_5|Hepatocellular_carcinoma|Lung_carcinoma|Seborrheic_keratosis|Epidermal_nevus|Neoplasm_of_stomach|Ovarian_neoplasm|CLAPO_syndrome": 1,
    "CLAPO_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "PIK3CA-related_disorder|Cowden_syndrome": 2,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 10,
    "Inborn_genetic_diseases|Cowden_syndrome|Cowden_syndrome_5": 1,
    "Cowden_syndrome|Corpus_callosum|_agenesis_of|Ectopic_tissue|Focal-onset_seizure|Seizure": 1,
    "Cowden_syndrome|PIK3CA-related_disorder": 1,
    "CLOVES_syndrome": 2,
    "Cowden_syndrome|Cowden_syndrome_5|Inborn_genetic_diseases|not_provided": 1,
    "Cowden_syndrome|PIK3CA-related_disorder|Inborn_genetic_diseases": 1,
    "Megalencephaly|_autosomal_dominant|Abnormality_of_the_hairline|Hypertelorism|Intestinal_duplication|Diaphragmatic_eventration|Inborn_genetic_diseases|Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided|Cowden_syndrome_5": 1,
    "Noonan_syndrome_8|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "Gastric_cancer|Epidermal_nevus|Ovarian_neoplasm|Cowden_syndrome_5|Lung_cancer|Familial_cancer_of_breast|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Hepatocellular_carcinoma|Congenital_macrodactylia|Seborrheic_keratosis|CLAPO_syndrome|Colorectal_cancer|CLOVES_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided|Abnormal_cardiovascular_system_morphology": 1,
    "not_provided|PIK3CA_related_overgrowth_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "not_provided|PIK3CA_related_overgrowth_syndrome|Inborn_genetic_diseases": 1,
    "PIK3CA-related_disorder|Cowden_syndrome_5|Cowden_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Cowden_syndrome|Overgrowth|Facial_asymmetry|Hemimegalencephaly": 1,
    "Cowden_syndrome|not_provided|not_specified|Cowden_syndrome_5": 1,
    "Cowden_syndrome_1|PIK3CA-related_disorder|Cowden_syndrome": 1,
    "Inborn_genetic_diseases|Seborrheic_keratosis|Ovarian_cancer|Familial_cancer_of_breast|Hemifacial_myohyperplasia|Cerebral_cavernous_malformation_4|Cowden_syndrome_5|Hepatocellular_carcinoma|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Epidermal_nevus|CLAPO_syndrome|Colorectal_cancer|Gastric_cancer|CLOVES_syndrome|Lung_cancer|Cowden_syndrome": 1,
    "PIK3CA_related_overgrowth_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|not_provided": 1,
    "Cowden_syndrome|PIK3CA-related_disorder|PIK3CA_related_overgrowth_syndrome|Angioosteohypertrophic_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Ovarian_neoplasm": 1,
    "Inborn_genetic_diseases|PIK3CA-related_disorder|Cowden_syndrome": 1,
    "Cowden_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "CLAPO_syndrome|CLOVES_syndrome|Cowden_syndrome_5|Familial_cancer_of_breast|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Lung_carcinoma|Seborrheic_keratosis|Carcinoma_of_colon|Hepatocellular_carcinoma|Congenital_macrodactylia|Epidermal_nevus|Ovarian_neoplasm|Neoplasm_of_stomach|PIK3CA-related_disorder|Cowden_syndrome": 1,
    "Klippel-Tr\u00c3\u00a9naunay_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|CLOVES_syndrome|Inborn_genetic_diseases|Capillary_malformation": 1,
    "PIK3CA_related_overgrowth_syndrome|Cowden_syndrome|PIK3CA-related_disorder|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Epidermal_nevus": 1,
    "Inborn_genetic_diseases|Cowden_syndrome|not_specified|not_provided|Cowden_syndrome_5": 1,
    "not_provided|Cowden_syndrome_5": 1,
    "not_provided|Cowden_syndrome_1": 9,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Cowden_syndrome|not_specified|not_provided|Cowden_syndrome_5": 1,
    "Familial_cancer_of_breast|Cowden_syndrome_5|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Seborrheic_keratosis|Hemifacial_myohyperplasia|Epidermal_nevus|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Ovarian_cancer|Cerebral_cavernous_malformation_4|Lung_cancer|CLAPO_syndrome|CLOVES_syndrome": 1,
    "PIK3CA-related_disorder|PIK3CA_related_overgrowth_syndrome|not_specified|CLOVES_syndrome": 1,
    "CLAPO_syndrome|Rare_combined_vascular_malformation|Cowden_syndrome|Colorectal_cancer|PIK3CA_related_overgrowth_syndrome|not_provided|CLOVES_syndrome|Capillary_malformation|Ovarian_neoplasm|Segmental_undergrowth_associated_with_lymphatic_malformation|Abnormal_cardiovascular_system_morphology": 1,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|PIK3CA_related_overgrowth_syndrome": 1,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|not_provided": 1,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|PIK3CA_related_overgrowth_syndrome": 2,
    "Cowden_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|not_provided": 1,
    "PIK3CA_related_overgrowth_syndrome|PIK3CA-related_disorder|Cowden_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|CLOVES_syndrome|Ovarian_neoplasm|Abnormal_cardiovascular_system_morphology": 1,
    "Non-small_cell_lung_carcinoma": 29,
    "Hemifacial_myohyperplasia|CLAPO_syndrome|CLOVES_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Seborrheic_keratosis|Ovarian_cancer|Cerebral_cavernous_malformation_4|Familial_cancer_of_breast|Epidermal_nevus|Cowden_syndrome_5|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Lung_cancer": 3,
    "Inborn_genetic_diseases|Cowden_syndrome|not_provided": 4,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|CLAPO_syndrome|CLOVES_syndrome|Gastric_cancer|Cerebral_cavernous_malformation_4|Familial_cancer_of_breast|Hemifacial_myohyperplasia|Seborrheic_keratosis|Epidermal_nevus|Cowden_syndrome_5|Hepatocellular_carcinoma|Colorectal_cancer|Ovarian_cancer|Lung_cancer|PIK3CA-related_disorder|Cowden_syndrome": 1,
    "Cowden_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|CLAPO_syndrome|CLOVES_syndrome|Gastric_cancer|Cerebral_cavernous_malformation_4|Familial_cancer_of_breast|Hemifacial_myohyperplasia|Seborrheic_keratosis|Epidermal_nevus|Cowden_syndrome_5|Hepatocellular_carcinoma|Colorectal_cancer|Ovarian_cancer|Lung_cancer|Cowden_syndrome": 1,
    "not_specified|Cowden_syndrome|Inborn_genetic_diseases": 1,
    "PIK3CA-related_disorder|Cowden_syndrome|not_provided": 1,
    "Cowden_syndrome_5|not_provided": 1,
    "Lip_and_oral_cavity_carcinoma|CLAPO_syndrome|PIK3CA-related_overgrowth|HEMIFACIAL_MYOHYPERPLASIA|_SOMATIC|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|CEREBRAL_CAVERNOUS_MALFORMATIONS_4|_SOMATIC|Cerebrofacial_Vascular_Metameric_Syndrome_(CVMS)|Rare_venous_malformation|PIK3CA-related_disorder|Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|CLOVES_syndrome|Ovarian_neoplasm|Non-small_cell_lung_carcinoma|Abnormal_cardiovascular_system_morphology": 1,
    "HEMIFACIAL_MYOHYPERPLASIA|_SOMATIC|Rare_combined_vascular_malformation|Rare_venous_malformation|Gallbladder_cancer|PIK3CA_overgrowth_syndrome|Eccrine_angiomatous_hamartoma|Cerebrofacial_Vascular_Metameric_Syndrome_(CVMS)|PIK3CA_related_overgrowth_syndrome|Gastric_cancer|Sarcoma|Angioosteohypertrophic_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|CLOVES_syndrome|Seborrheic_keratosis|Ovarian_neoplasm|OVARIAN_CANCER|_EPITHELIAL|_SOMATIC|Non-small_cell_lung_carcinoma|Carcinoma_of_colon|Breast_adenocarcinoma|Segmental_undergrowth_associated_with_lymphatic_malformation|Abnormal_cardiovascular_system_morphology": 1,
    "Histone_Methylation_Therapy_response": 1,
    "PIK3CA_related_overgrowth_syndrome|Ovarian_neoplasm|Hepatocellular_carcinoma|Abnormal_cardiovascular_system_morphology": 1,
    "Carcinoma_of_colon|Epidermal_nevus|PIK3CA_related_overgrowth_syndrome": 1,
    "PIK3CA_related_overgrowth_syndrome|Capillary_malformation|Cowden_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "PIK3CA_related_overgrowth_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Ovarian_neoplasm|OVARIAN_CANCER|_EPITHELIAL|_SOMATIC|Prostate_cancer|Carcinoma_of_colon|Segmental_undergrowth_associated_with_mainly_venous_malformation_with_capillary_component": 1,
    "Breast_adenocarcinoma|PIK3CA_related_overgrowth_syndrome": 1,
    "PIK3CA_related_overgrowth_syndrome|Ovarian_neoplasm": 1,
    "PIK3CA_related_overgrowth_syndrome|not_provided|Ovarian_neoplasm|Abnormal_cardiovascular_system_morphology": 1,
    "Cowden_syndrome|Familial_cancer_of_breast": 1,
    "Cowden_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome|Inborn_genetic_diseases|not_provided|Cowden_syndrome_5": 1,
    "Inborn_genetic_diseases|Cowden_syndrome_1": 1,
    "not_provided|Cowden_syndrome|not_specified|Cowden_syndrome_5": 1,
    "Cowden_syndrome_1|Cowden_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Cowden_syndrome_1|Cowden_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Cowden_syndrome|not_provided|Cowden_syndrome_5": 1,
    "Cowden_syndrome|Cowden_syndrome_1": 2,
    "Familial_cancer_of_breast|Hemifacial_myohyperplasia|Seborrheic_keratosis|Epidermal_nevus|CLAPO_syndrome|CLOVES_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Cerebral_cavernous_malformation_4|Cowden_syndrome_5|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Lung_cancer|Ovarian_cancer|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_5|Cerebral_cavernous_malformation_4|Ovarian_cancer|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Gastric_cancer|Epidermal_nevus|Familial_cancer_of_breast|CLOVES_syndrome|Congenital_macrodactylia|Colorectal_cancer|CLAPO_syndrome|Seborrheic_keratosis|Hemifacial_myohyperplasia|Hepatocellular_carcinoma|Lung_cancer": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Cowden_syndrome|not_provided": 1,
    "not_specified|Cowden_syndrome|not_provided|Cowden_syndrome_1": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Cowden_syndrome|Inborn_genetic_diseases": 1,
    "Ovarian_cancer|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Seborrheic_keratosis|Epidermal_nevus|Cerebral_cavernous_malformation_4|Lung_cancer|Cowden_syndrome_5|Hepatocellular_carcinoma|Familial_cancer_of_breast|CLAPO_syndrome|CLOVES_syndrome|Hemifacial_myohyperplasia|Colorectal_cancer|Gastric_cancer|Cowden_syndrome": 1,
    "Glycogen_storage_disease|_type_II": 1776,
    "Megalencephaly-capillary_malformation-polymicrogyria_syndrome|PIK3CA-related_disorder": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Inborn_genetic_diseases|Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "Cowden_syndrome|not_provided|Inborn_genetic_diseases|Cowden_syndrome_5": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Cowden_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome": 2,
    "not_specified|Cowden_syndrome_5|Cowden_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_1|Cowden_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "PIK3CA-related_disorder|Cowden_syndrome|Inborn_genetic_diseases": 1,
    "PIK3CA-related_disorder|Inborn_genetic_diseases|Cowden_syndrome": 1,
    "PIK3CA-related_disorder|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_5|Cowden_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|PIK3CA-related_disorder|Cowden_syndrome": 1,
    "Cowden_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Congenital_macrodactylia|Lung_cancer|Familial_cancer_of_breast|CLOVES_syndrome|Cowden_syndrome_5|Hepatocellular_carcinoma|Colorectal_cancer|Seborrheic_keratosis|Epidermal_nevus|Gastric_cancer|Ovarian_neoplasm|CLAPO_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PIK3CA_related_overgrowth_syndrome|PIK3C1-related_disorder|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Cowden_syndrome|PIK3CA-related_disorder|Angioosteohypertrophic_syndrome|not_provided|CLOVES_syndrome|Cowden_syndrome_5|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Abnormal_cardiovascular_system_morphology|Abnormal_cerebral_morphology": 1,
    "Segmental_undergrowth_associated_with_mainly_venous_malformation_with_capillary_component|See_cases|Angioosteohypertrophic_syndrome|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|not_provided": 1,
    "not_provided|PIK3CA-related_disorder": 1,
    "not_provided|CLAPO_syndrome|CLOVES_syndrome|Lung_cancer|Cowden_syndrome_5|Familial_cancer_of_breast|Seborrheic_keratosis|Congenital_macrodactylia|Cerebral_cavernous_malformation_4|Hemifacial_myohyperplasia|Epidermal_nevus|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Ovarian_cancer|Hepatocellular_carcinoma|Colorectal_cancer|Gastric_cancer": 1,
    "not_provided|Cowden_syndrome|Cowden_syndrome_5": 1,
    "PIK3CA_related_overgrowth_syndrome|not_provided": 1,
    "Cowden_syndrome|PIK3CA_related_overgrowth_syndrome": 1,
    "Cowden_syndrome|Abnormal_cardiovascular_system_morphology": 1,
    "Non-small_cell_lung_carcinoma|PIK3CA_related_overgrowth_syndrome|not_provided|CLOVES_syndrome": 1,
    "Cowden_syndrome|not_specified|not_provided|Cowden_syndrome_5": 1,
    "PIK3CA_related_overgrowth_syndrome|Cowden_syndrome|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Non-small_cell_lung_carcinoma": 1,
    "not_provided|PIK3CA_related_overgrowth_syndrome|Cowden_syndrome": 1,
    "Angioosteohypertrophic_syndrome|Cowden_syndrome": 1,
    "PIK3CA_overgrowth_syndrome|HEMIFACIAL_MYOHYPERPLASIA|_SOMATIC|Congenital_macrodactylia|CLAPO_syndrome|CLOVES_syndrome|Familial_cancer_of_breast|Seborrheic_keratosis|Epidermal_nevus|Carcinoma_of_colon|Cowden_syndrome_5|Ovarian_neoplasm|Hepatocellular_carcinoma|Lung_carcinoma|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Neoplasm_of_stomach|Inborn_genetic_diseases|Cowden_syndrome|PIK3CA_related_overgrowth_syndrome|not_provided|Non-small_cell_lung_carcinoma|Segmental_undergrowth_associated_with_mainly_venous_malformation_with_capillary_component": 1,
    "PIK3CA-related_disorder|MACRODACTYLY|_SOMATIC|Congenital_macrodactylia|CLAPO_syndrome|Rare_combined_vascular_malformation|Rare_venous_malformation|Rosette-forming_glioneuronal_tumor|PIK3CA-Related_Overgrowth_Spectrum_Disorders|Klippel-Trenaunay-like-Syndrome|Cerebrofacial_Vascular_Metameric_Syndrome_(CVMS)|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|CEREBRAL_CAVERNOUS_MALFORMATIONS_4|_SOMATIC|PIK3CA_related_overgrowth_syndrome|Lip_and_oral_cavity_carcinoma|Gastric_cancer|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Seborrheic_keratosis|Hepatocellular_carcinoma|CLOVES_syndrome|Ovarian_neoplasm|Non-small_cell_lung_carcinoma|OVARIAN_CANCER|_EPITHELIAL|_SOMATIC|Carcinoma_of_colon|Breast_adenocarcinoma|Abnormal_cardiovascular_system_morphology|Segmental_undergrowth_associated_with_mainly_venous_malformation_with_capillary_component|Segmental_undergrowth_associated_with_lymphatic_malformation|Breast_carcinoma": 1,
    "CEREBRAL_CAVERNOUS_MALFORMATIONS_4|_SOMATIC|Colorectal_cancer|Cowden_syndrome_1|Stroke_disorder|Macrodactyly_of_toe|Inborn_genetic_diseases|Cavernous_lymphangioma|Breast_adenocarcinoma|CLOVES_syndrome|not_provided|CLAPO_syndrome|Ovarian_neoplasm|Hemihypertrophy|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|PIK3CA_related_overgrowth_syndrome": 1,
    "not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome": 1,
    "Arteriovenous_malformation": 8,
    "Gastric_cancer|PIK3CA_related_overgrowth_syndrome|Hepatocellular_carcinoma": 1,
    "Lymphatic_malformation": 5,
    "PIK3CA-related_disorder|not_provided|Cowden_syndrome": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_F": 190,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_F|not_provided": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_F": 22,
    "GNB4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_F|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_F": 7,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_F|not_provided|Inborn_genetic_diseases": 1,
    "GNB4-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_F": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_F|Inborn_genetic_diseases": 7,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_F|not_specified": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_F|not_provided": 2,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_F|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_F": 3,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_F": 1,
    "GNB4-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_F|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Inborn_genetic_diseases": 1,
    "ACTL6A-related_BAFopathy": 1,
    "ACTL6A-related_disorder|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Delayed_speech_and_language_development": 1,
    "Broad_thumb|Delayed_speech_and_language_development|Inguinal_hernia|Syncope|Coarse_facial_features|Umbilical_hernia|Gastroesophageal_reflux|Recurrent_otitis_media|Broad_nasal_tip|Cleft_anterior_mitral_valve_leaflet|Aplasia/Hypoplasia_of_the_nails|Torticollis|Atrial_septal_defect|not_provided|ACTL6A-related_intellectual_disability|_autosomal_dominant|BAFopathy|ACTL6A-related_BAFopathy": 1,
    "ACTL6A-related_BAFopathy|not_provided": 1,
    "Delayed_speech_and_language_development|Global_developmental_delay": 3,
    "TTC14-related_disorder": 8,
    "TTC14-related_disorder|not_specified": 1,
    "Primary_ciliary_dyskinesia_14": 63,
    "not_provided|Primary_ciliary_dyskinesia_14": 2,
    "Primary_ciliary_dyskinesia_14|not_provided": 1,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_14": 2,
    "Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia": 34,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14": 23,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14|not_provided|not_specified": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia": 71,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14|not_provided": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14": 3,
    "Fibrous_Sheath_Dysplasia": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14": 13,
    "Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia|not_provided": 2,
    "Primary_ciliary_dyskinesia|CCDC39-related_disorder|Primary_ciliary_dyskinesia_14": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14|not_specified": 1,
    "Primary_ciliary_dyskinesia|not_specified": 183,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Primary_ciliary_dyskinesia_14": 1,
    "CCDC39-related_disorder|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_14": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_14": 3,
    "Primary_ciliary_dyskinesia_14|not_provided|Primary_ciliary_dyskinesia": 3,
    "Primary_ciliary_dyskinesia_14|CCDC39-related_disorder|not_specified|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14": 3,
    "not_specified|Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|CCDC39-related_disorder|not_specified|Primary_ciliary_dyskinesia_14": 1,
    "Heterotaxy|CCDC39-related_disorder|Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_14|CCDC39-related_disorder|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|CCDC39-related_disorder": 4,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14|Ellis-van_Creveld_syndrome": 1,
    "Primary_ciliary_dyskinesia_14|not_specified|not_provided|Primary_ciliary_dyskinesia|CCDC39-related_disorder": 2,
    "Primary_ciliary_dyskinesia|Respiratory_ciliopathies_including_non-CF_bronchiectasis": 3,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia|not_specified": 29,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14": 1,
    "Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia|not_specified": 1,
    "CCDC39-related_disorder|Primary_ciliary_dyskinesia": 3,
    "CCDC39-related_disorder|Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis": 10,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14|CCDC39-related_disorder": 1,
    "Primary_ciliary_dyskinesia_14|CCDC39-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_14": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_14|not_specified": 1,
    "Infertility_disorder|not_provided|Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia|CCDC39-related_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia|CCDC39-related_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia_14|Primary_ciliary_dyskinesia": 1,
    "Myopathy|_congenital|_with_respiratory_insufficiency_and_bone_fractures": 2,
    "Myopathy|_congenital|_with_respiratory_insufficiency_and_bone_fractures|Myopathy|_congenital_proximal|_with_minicore_lesions|not_provided": 1,
    "Delayed_gross_motor_development|Neonatal_respiratory_distress|Scoliosis": 1,
    "Myopathy|_congenital_proximal|_with_minicore_lesions": 2,
    "Myopathy|_congenital_proximal|_with_minicore_lesions|Multiminicore_myopathy": 1,
    "3-methylglutaconic_aciduria_type_5": 95,
    "Inborn_genetic_diseases|not_specified|not_provided|3-methylglutaconic_aciduria_type_5": 1,
    "not_provided|3-methylglutaconic_aciduria_type_5": 4,
    "3-methylglutaconic_aciduria_type_5|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|3-methylglutaconic_aciduria_type_5": 2,
    "DNAJC19-related_disorder": 2,
    "not_provided|3-methylglutaconic_aciduria_type_5|not_specified": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_5|not_specified": 1,
    "3-methylglutaconic_aciduria_type_5|not_specified": 2,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_5": 2,
    "3-methylglutaconic_aciduria_type_5|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|3-methylglutaconic_aciduria_type_5|Inborn_genetic_diseases": 1,
    "3-methylglutaconic_aciduria_type_5|DNAJC19-related_disorder": 1,
    "not_specified|3-methylglutaconic_aciduria_type_5": 3,
    "3-methylglutaconic_aciduria_type_5|3-Methylglutaconic_aciduria_type_3": 1,
    "3-Methylglutaconic_aciduria": 2,
    "3-methylglutaconic_aciduria_type_5|not_provided": 1,
    "not_specified|DNAJC19-related_disorder": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 117,
    "Congenital_aniridia|not_provided": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|SOX2-related_disorder": 3,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|not_provided": 8,
    "not_provided|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 9,
    "SOX2-related_disorder|not_provided|Anophthalmia/microphthalmia-esophageal_atresia_syndrome|Septo-optic_dysplasia_sequence": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Amenorrhea|not_provided|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 4,
    "not_specified|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 1,
    "Chorioretinal_coloboma": 1,
    "SOX2-related_disorder": 3,
    "not_specified|not_provided|Anophthalmia/microphthalmia-esophageal_atresia_syndrome|SOX2-related_disorder": 1,
    "Anophthalmia": 6,
    "Cataract_-_microcornea_syndrome": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|Optic_nerve_hypoplasia_and_abnormalities_of_the_central_nervous_system": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|not_provided|not_specified": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|not_specified": 2,
    "Anophthalmia|not_provided": 1,
    "Anophthalmia/microphthalmia-esophageal_atresia_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Anophthalmia/microphthalmia-esophageal_atresia_syndrome|Optic_nerve_hypoplasia_and_abnormalities_of_the_central_nervous_system": 1,
    "Inborn_genetic_diseases|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 1,
    "not_specified|not_provided|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency": 636,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided": 13,
    "MCCC1-related_disorder|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 10,
    "not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_specified": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_specified": 10,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 14,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 10,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|MCCC1-related_disorder": 1,
    "Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 9,
    "not_provided|MCCC1-related_disorder|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases": 7,
    "MCCC1-related_disorder|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 24,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|MCCC1-related_disorder": 1,
    "not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 6,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|MCCC1-related_disorder": 8,
    "Inborn_genetic_diseases|not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|Inborn_genetic_diseases": 2,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_1_deficiency|MCCC1-related_disorder": 2,
    "MCCC1-related_disorder": 4,
    "Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 3,
    "Inborn_genetic_diseases|MCCC1-related_disorder|not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "not_specified|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 2,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided|not_specified": 2,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|MCCC1-related_disorder": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency": 15,
    "Methylcrotonyl-CoA_carboxylase_deficiency|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 3,
    "Methylcrotonyl-CoA_carboxylase_deficiency|Inborn_genetic_diseases|MCCC1-related_disorder|not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "MCCC1-related_disorder|not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 2,
    "Methylcrotonyl-CoA_carboxylase_deficiency|not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 2,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_specified|MCCC1-related_disorder": 1,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 5,
    "Methylcrotonyl-CoA_carboxylase_deficiency|Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|MCCC1-related_disorder|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided|MCCC1-related_disorder|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|not_provided": 1,
    "not_provided|MCCC1-related_disorder|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided": 2,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_1_deficiency|Inborn_genetic_diseases": 1,
    "3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_specified|not_provided": 1,
    "not_provided|not_specified|3-methylcrotonyl-CoA_carboxylase_1_deficiency": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_1_deficiency|not_provided": 1,
    "LAMP3-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_6|_generalized|_with_scarring_and_hair_loss|not_provided|KLHL24-related_disorder|Epidermolysis_bullosa_simplex|_Koebner_type": 1,
    "Epidermolysis_bullosa_simplex_6|_generalized|_with_scarring_and_hair_loss|Epidermolysis_bullosa_simplex|_Koebner_type": 3,
    "Epidermolysis_bullosa_simplex_6|_generalized|_with_scarring_and_hair_loss": 7,
    "KLHL24-related_disorder": 2,
    "Cardiomyopathy|_familial_hypertrophic|_29|_with_polyglucosan_bodies": 4,
    "Inborn_genetic_diseases|Cardiomyopathy|_familial_hypertrophic|_29|_with_polyglucosan_bodies": 2,
    "not_provided|KLHL24-related_disorder": 3,
    "KLHL24-related_disorder|not_provided": 1,
    "Cardiomyopathy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KLHL24-related_disorder|not_provided": 1,
    "not_specified|Epilepsy|_familial_adult_myoclonic|_4": 3,
    "not_provided|Epilepsy|_familial_adult_myoclonic|_4": 3,
    "Epilepsy|_familial_adult_myoclonic|_4": 11,
    "Benign_adult_familial_myoclonic_epilepsy": 1,
    "not_specified|YEATS2-related_disorder": 2,
    "Epilepsy|_familial_adult_myoclonic|_4|not_provided": 1,
    "YEATS2-related_disorder": 3,
    "MAP6D1-related_disorder": 4,
    "Leukoencephalopathy_with_vanishing_white_matter_5": 15,
    "EIF2B5-related_disorder": 1,
    "EIF2B5-related_disorder|not_provided": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_5|not_provided|not_specified": 1,
    "not_provided|EIF2B5-related_disorder|Leukoencephalopathy_with_vanishing_white_matter_5": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_5|not_provided": 1,
    "Vanishing_white_matter_disease|not_provided|EIF2B5-related_disorder|Leukoencephalopathy_with_vanishing_white_matter_1|Leukoencephalopathy_with_vanishing_white_matter_5|Inborn_genetic_diseases": 1,
    "Vanishing_white_matter_disease|See_cases|EIF2B5-related_disorder|Inborn_genetic_diseases|Leukoencephalopathy_with_vanishing_white_matter_5|not_provided": 1,
    "Inborn_genetic_diseases|Vanishing_white_matter_disease|not_provided": 1,
    "not_provided|Vanishing_white_matter_disease|EIF2B5-related_disorder": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_5|not_provided": 2,
    "EIF2B5-related_disorder|not_provided|Vanishing_white_matter_disease": 1,
    "Inborn_genetic_diseases|not_provided|Leukoencephalopathy_with_vanishing_white_matter_5": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_5|not_provided|Vanishing_white_matter_disease": 3,
    "Leukoencephalopathy_with_vanishing_white_matter_1|Leukoencephalopathy_with_vanishing_white_matter_5|not_provided|Vanishing_white_matter_disease": 1,
    "not_provided|Leukoencephalopathy_with_vanishing_white_matter_5": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1|Leukoencephalopathy_with_vanishing_white_matter_5": 1,
    "Vanishing_white_matter_disease|not_provided|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "not_provided|Leukoencephalopathy_with_vanishing_white_matter_5|Vanishing_white_matter_disease": 2,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_5": 1,
    "Leukodystrophy|not_provided|Vanishing_white_matter_disease": 1,
    "not_provided|Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_5": 2,
    "Vanishing_white_matter_disease|not_specified": 2,
    "Leukoencephalopathy_with_vanishing_white_matter_5|Vanishing_white_matter_disease|not_provided": 2,
    "Vanishing_white_matter_disease|not_provided|Leukoencephalopathy_with_vanishing_white_matter_5": 1,
    "not_provided|EIF2B5-related_disorder": 2,
    "Ovarioleukodystrophy|Vanishing_white_matter_disease": 1,
    "not_provided|Inborn_genetic_diseases|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "not_specified|not_provided|EIF2B5-related_disorder|Vanishing_white_matter_disease": 1,
    "not_provided|EIF2B5-related_disorder|Vanishing_white_matter_disease": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_1|not_provided": 2,
    "Leukoencephalopathy": 1,
    "not_provided|DVL3-related_disorder": 8,
    "Autosomal_dominant_Robinow_syndrome_3": 18,
    "DVL3-related_disorder": 9,
    "not_provided|not_specified|DVL3-related_disorder": 1,
    "DVL3-related_disorder|not_provided": 5,
    "Midface_retrusion|Lumbar_hyperlordosis|Short_toe|Genu_valgum|Dental_crowding|Anteverted_nares|Clinodactyly_of_the_5th_finger|Short_stature|Neurodevelopmental_delay|Short_finger|Tented_upper_lip_vermilion": 1,
    "Autosomal_dominant_Robinow_syndrome_3|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|DVL3-related_disorder": 1,
    "not_provided|Autosomal_dominant_Robinow_syndrome_3|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Robinow_syndrome_3|not_provided": 1,
    "not_provided|Autosomal_dominant_Robinow_syndrome_3": 2,
    "DVL3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_Robinow_syndrome_1|Autosomal_dominant_Robinow_syndrome_2|Autosomal_dominant_Robinow_syndrome_3": 5,
    "AP2M1-related_disorder|not_provided": 1,
    "AP2M1-related_disorder": 1,
    "not_provided|Intellectual_developmental_disorder_60_with_seizures|AP2M1-related_disorder|not_specified": 1,
    "not_provided|AP2M1-related_disorder": 2,
    "not_provided|Intellectual_developmental_disorder_60_with_seizures|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_60_with_seizures|not_provided": 1,
    "Intellectual_developmental_disorder_60_with_seizures|not_specified|not_provided|AP2M1-related_disorder": 1,
    "Intellectual_developmental_disorder_60_with_seizures|not_specified|not_provided": 1,
    "Intellectual_developmental_disorder_60_with_seizures|not_provided|AP2M1-related_disorder": 1,
    "AP2M1-related_disorder|Intellectual_developmental_disorder_60_with_seizures|not_provided": 1,
    "ALG3-congenital_disorder_of_glycosylation": 110,
    "not_provided|ALG3-congenital_disorder_of_glycosylation|not_specified": 3,
    "ALG3-related_disorder": 6,
    "Inborn_genetic_diseases|ALG3-congenital_disorder_of_glycosylation|not_provided": 2,
    "not_specified|ALG3-congenital_disorder_of_glycosylation": 6,
    "not_specified|not_provided|ALG3-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|ALG3-congenital_disorder_of_glycosylation": 12,
    "ALG3-congenital_disorder_of_glycosylation|ALG3-related_disorder": 3,
    "ALG3-congenital_disorder_of_glycosylation|not_specified": 2,
    "ALG3-congenital_disorder_of_glycosylation|not_provided": 8,
    "ALG3-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 2,
    "not_provided|ALG3-congenital_disorder_of_glycosylation": 10,
    "Intellectual_disability|ALG3-congenital_disorder_of_glycosylation|not_specified": 1,
    "ALG3-related_disorder|ALG3-congenital_disorder_of_glycosylation": 1,
    "ALG3-congenital_disorder_of_glycosylation|ALG3-related_disorder|not_specified": 1,
    "not_provided|ALG3-congenital_disorder_of_glycosylation|ALG3-related_disorder": 1,
    "ALG3-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "not_provided|ALG3-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "not_specified|ALG3-congenital_disorder_of_glycosylation|not_provided": 1,
    "ALG3-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|ALG3-congenital_disorder_of_glycosylation": 1,
    "not_provided|ALG3-related_disorder": 1,
    "EIF4G1-related_disorder": 14,
    "EIF4G1-related_disorder|not_specified": 3,
    "Parkinson_disease_18|_autosomal_dominant|_susceptibility_to": 9,
    "Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_specified": 2,
    "not_provided|Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_specified": 1,
    "not_provided|EIF4G1-related_disorder": 2,
    "EIF4G1-related_disorder|Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "not_specified|Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "not_provided|Parkinson_disease_18|_autosomal_dominant|_susceptibility_to": 1,
    "not_specified|EIF4G1-related_disorder": 1,
    "EIF4G1-related_disorder|not_provided": 1,
    "EIF4G1-related_disorder|not_specified|not_provided": 3,
    "Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_specified|not_provided": 1,
    "Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_provided|not_specified": 1,
    "Parkinson_disease_18|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "FAM131A-related_disorder": 3,
    "CLCN2-related_disorder": 8,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 12,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 2,
    "not_provided|Inborn_genetic_diseases|Epilepsy": 3,
    "Familial_hyperaldosteronism_type_II": 8,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II": 62,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|not_provided": 9,
    "not_provided|Hereditary_ataxia|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "not_provided|not_specified|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II": 1,
    "Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided": 4,
    "not_provided|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II": 1,
    "not_provided|CLCN2-related_disorder": 4,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II": 2,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II": 1,
    "not_provided|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|not_provided": 4,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 17,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|not_specified": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Intellectual_disability": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Inborn_genetic_diseases": 1,
    "CLCN2-related_disorder|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Intellectual_disability": 1,
    "not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II": 1,
    "not_specified|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_specified|not_provided": 3,
    "Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Inborn_genetic_diseases|not_provided": 2,
    "EPILEPSY|_JUVENILE_ABSENCE|_SUSCEPTIBILITY_TO|_2|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 1,
    "Hereditary_ataxia|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "CLCN2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided": 1,
    "not_provided|Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|not_provided|Seizure": 1,
    "Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|not_provided": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II": 3,
    "CLCN2-related_disorder|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|not_provided": 1,
    "Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 2,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II": 1,
    "Inborn_genetic_diseases|CLCN2-related_disorder|not_provided": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 1,
    "CLCN2-related_disorder|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|not_specified|not_provided|Cerebral_palsy": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided": 6,
    "CLCN2-related_disorder|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|not_provided": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 2,
    "Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|See_cases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases|not_provided": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 4,
    "Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Inborn_genetic_diseases": 4,
    "CLCN2-related_disorder|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|CLCN2-related_disorder|not_provided": 1,
    "CLCN2-related_disorder|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Familial_hyperaldosteronism_type_II": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hyperaldosteronism_type_II": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|not_provided|CLCN2-related_disorder": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|CLCN2-related_disorder": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|not_provided|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|CLCN2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|CLCN2-related_disorder": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II": 2,
    "not_provided|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 1,
    "Inborn_genetic_diseases|Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema": 1,
    "CLCN2-related_disorder|Inborn_genetic_diseases": 1,
    "Cerebellar_ataxia|CNS_demyelination|Spastic_gait|Bipolar_affective_disorder": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Inborn_genetic_diseases": 2,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Inborn_genetic_diseases|See_cases": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|not_specified|not_provided|EPILEPSY|_JUVENILE_MYOCLONIC|_SUSCEPTIBILITY_TO|_8": 1,
    "not_provided|CLCN2-related_disorder|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "not_provided|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Familial_hyperaldosteronism_type_II|CLCN2-related_disorder": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|EPILEPSY|_JUVENILE_MYOCLONIC|_SUSCEPTIBILITY_TO|_8": 1,
    "Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|not_provided": 1,
    "Familial_hyperaldosteronism_type_II|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Seizure": 1,
    "Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "CLCN2-related_disorder|not_specified|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|not_provided": 1,
    "not_provided|Familial_hyperaldosteronism_type_II|Leukoencephalopathy_with_mild_cerebellar_ataxia_and_white_matter_edema|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_11": 1,
    "Familial_hyperaldosteronism_type_II|not_provided": 1,
    "Thrombocythemia_1": 18,
    "not_provided|Thrombocythemia_1": 8,
    "Thrombocythemia_1|not_provided": 6,
    "Thrombocythemia_1|not_specified|not_provided": 1,
    "THPO-related_disorder|not_provided": 2,
    "Thrombocythemia_1|not_provided|Inborn_genetic_diseases|THPO-related_disorder": 1,
    "THPO-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Thrombocythemia_1|Thrombocytopenia_9|Amegakaryocytic_thrombocytopenia|_congenital|_2": 1,
    "Thrombocythemia_1|Amegakaryocytic_thrombocytopenia|_congenital|_2|Thrombocytopenia_9": 1,
    "Thrombocythemia_1|Inborn_genetic_diseases|not_provided": 1,
    "Thrombocytopenia_9|Macrothrombocytopenia": 1,
    "not_provided|Thrombocythemia_1|Amegakaryocytic_thrombocytopenia|_congenital|_2|Thrombocytopenia_9": 1,
    "Inborn_genetic_diseases|THPO-related_disorder|not_provided": 1,
    "Macrothrombocytopenia|Abnormal_bleeding|Thrombocytopenia|Thrombocytopenia_9": 1,
    "Thrombocythemia_1|Amegakaryocytic_thrombocytopenia|_congenital|_2|Thrombocytopenia_9|Inborn_genetic_diseases": 1,
    "THPO-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Thrombocythemia_1": 1,
    "not_provided|Amegakaryocytic_thrombocytopenia|_congenital|_2|Thrombocytopenia": 1,
    "Thrombocytopenia_9|Amegakaryocytic_thrombocytopenia|_congenital|_2|Thrombocythemia_1": 1,
    "not_provided|Thrombocythemia_1|Inborn_genetic_diseases": 1,
    "Amegakaryocytic_thrombocytopenia|_congenital|_2|not_provided": 1,
    "Thrombocytopenia_9|Amegakaryocytic_thrombocytopenia|_congenital|_2|not_provided": 1,
    "Thrombocythemia_1|not_provided|not_specified": 1,
    "Amegakaryocytic_thrombocytopenia|_congenital|_2|Inborn_genetic_diseases": 1,
    "Thrombocytopenia_9|Thrombocytopenia": 1,
    "THPO-related_disorder": 3,
    "not_provided|Thrombocythemia_1|Thrombocytopenia_9|Amegakaryocytic_thrombocytopenia|_congenital|_2": 1,
    "Thrombocytopenia_9": 1,
    "not_provided|THPO-related_disorder": 1,
    "not_specified|not_provided|THPO-related_disorder": 1,
    "not_provided|Amegakaryocytic_thrombocytopenia|_congenital|_2|Thrombocythemia_1": 1,
    "Amegakaryocytic_thrombocytopenia|_congenital|_2": 1,
    "VPS8-related_disorder|not_provided": 1,
    "VPS8-related_disorder": 2,
    "EHHADH-related_disorder": 33,
    "not_specified|EHHADH-related_disorder": 5,
    "EHHADH-related_disorder|not_specified": 5,
    "EHHADH-related_disorder|not_specified|not_provided": 5,
    "Fanconi_renotubular_syndrome_3": 12,
    "EHHADH-related_disorder|not_provided": 22,
    "EHHADH-related_disorder|not_provided|not_specified": 4,
    "Fanconi_renotubular_syndrome_1": 8,
    "not_provided|EHHADH-related_disorder": 4,
    "not_specified|not_provided|EHHADH-related_disorder": 1,
    "EHHADH-related_disorder|Fanconi_renotubular_syndrome_3": 1,
    "Fanconi_renotubular_syndrome_3|EHHADH-related_disorder|not_provided": 1,
    "not_provided|not_specified|EHHADH-related_disorder": 1,
    "Cholestasis|not_provided": 1,
    "not_provided|EHHADH-related_disorder|Fanconi_renotubular_syndrome_3": 1,
    "EHHADH-related_disorder|Chronic_kidney_disease": 1,
    "not_provided|EHHADH-related_disorder|not_specified": 1,
    "EHHADH-related_disorder|Fanconi_renotubular_syndrome_3|not_specified": 1,
    "Fanconi_renotubular_syndrome_3|EHHADH-related_disorder|not_specified": 1,
    "not_provided|Fanconi_renotubular_syndrome_3": 1,
    "not_specified|EHHADH-related_disorder|not_provided": 1,
    "Hypotrichosis_7": 7,
    "Woolly_hair|_autosomal_recessive_2|_with_or_without_hypotrichosis|Hypotrichosis_7": 1,
    "LIPH-related_disorder|not_provided": 3,
    "not_provided|Hypotrichosis_7|Woolly_hair|_autosomal_recessive_2|_with_or_without_hypotrichosis": 2,
    "Hypotrichosis_simplex|Hypotrichosis_7|Woolly_hair|_autosomal_recessive_2|_with_or_without_hypotrichosis": 1,
    "Woolly_hair|_autosomal_recessive_2|_with_or_without_hypotrichosis|not_provided|Hypotrichosis_7|LIPH-related_disorder": 1,
    "not_provided|Hypotrichosis_7": 1,
    "Woolly_hair|_autosomal_recessive_2|_with_or_without_hypotrichosis": 1,
    "LIPH-related_disorder": 1,
    "not_provided|LIPH-related_disorder": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1": 177,
    "Diabetes_mellitus_type_2|_susceptibility_to": 10,
    "TRA2B-associated_epileptic_encephalopathy": 1,
    "TRA2B-related_condition": 1,
    "ETV5-related_disorder": 2,
    "ETV5-related_disorder|not_specified": 1,
    "Cataract_20_multiple_types": 22,
    "CRYGS-related_disorder": 4,
    "Cataract_20_multiple_types|not_provided": 2,
    "Inborn_genetic_diseases|Cataract_20_multiple_types": 2,
    "Cataract_20_multiple_types|not_specified": 1,
    "Retinitis_pigmentosa|Cataract_20_multiple_types": 1,
    "Cataract_20_multiple_types|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cataract_20_multiple_types": 1,
    "DNAJB11-related_disorder": 9,
    "Polycystic_kidney_disease|Renal_cyst": 1,
    "Polycystic_kidney_disease_6_with_or_without_polycystic_liver_disease": 21,
    "Autosomal_dominant_polycystic_kidney_disease": 513,
    "not_provided|Polycystic_kidney_disease_6_with_or_without_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_6_with_or_without_polycystic_liver_disease|Inborn_genetic_diseases": 1,
    "DNAJB11-related_disorder|not_provided": 5,
    "Polycystic_kidney_disease_6_with_or_without_polycystic_liver_disease|not_provided": 1,
    "DNAJB11-related_disorder|Inborn_genetic_diseases": 1,
    "DNAJB11-related_disorder|Polycystic_kidney_disease_6_with_or_without_polycystic_liver_disease": 1,
    "Alopecia-intellectual_disability_syndrome_1|not_provided": 1,
    "AHSG-related_disorder": 3,
    "RECLASSIFIED_-_AHSG_POLYMORPHISM": 1,
    "Alopecia-intellectual_disability_syndrome_1|not_provided|RECLASSIFIED_-_AHSG_POLYMORPHISM": 2,
    "AHSG-related_disorder|not_provided": 1,
    "not_provided|Alopecia-intellectual_disability_syndrome_1": 1,
    "Alopecia-intellectual_disability_syndrome_1": 1,
    "not_specified|Alopecia-intellectual_disability_syndrome_1": 1,
    "Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency|not_specified": 1,
    "Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency": 9,
    "HRG-related_disorder": 7,
    "not_provided|Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency|HRG-related_disorder|Thrombus": 1,
    "not_provided|Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency": 1,
    "Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency|Familial_early-onset_deep_venous_thrombosis": 1,
    "not_provided|HRG-related_disorder": 2,
    "HRG-related_disorder|Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency|not_provided": 1,
    "HRG-related_disorder|not_specified": 2,
    "not_provided|not_specified|HRG-related_disorder": 1,
    "HRG-related_disorder|not_provided": 1,
    "Hereditary_thrombophilia_due_to_congenital_histidine-rich_(poly-L)_glycoprotein_deficiency|not_provided": 2,
    "KNG1-related_disorder": 8,
    "Thrombus|not_specified": 1,
    "Angioedema|_hereditary|_6|KNG1-related_disorder": 1,
    "High_molecular_weight_kininogen_deficiency": 7,
    "not_specified|Hereditary_angioedema_with_normal_C1Inh": 1,
    "High_molecular_weight_kininogen_deficiency|KININOGEN_DEFICIENCY|_TOTAL": 1,
    "KNG1-related_disorder|not_specified": 1,
    "Angioedema|_hereditary|_6": 2,
    "Angioedema|_hereditary|_6|High_molecular_weight_kininogen_deficiency": 1,
    "EIF4A2-related_disorder": 12,
    "Neurodevelopmental_disorder_with_hypotonia_and_speech_delay|_with_or_without_seizures": 6,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia_and_speech_delay|_with_or_without_seizures|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_speech_delay|_with_or_without_seizures|Intellectual_disability_with_muscular_spams": 1,
    "EIF4A2-related_Neurodevelopmental_Syndrome": 1,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia_and_speech_delay|_with_or_without_seizures": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia_and_speech_delay|_with_or_without_seizures": 1,
    "Neurodevelopmental_delay|Neurodevelopmental_disorder_with_hypotonia_and_speech_delay|_with_or_without_seizures": 1,
    "Morimoto-Ryu-Malicdan_neuromuscular_syndrome": 10,
    "Morimoto-Ryu-Malicdan_neuromuscular_syndrome|not_specified": 1,
    "Adiponectin_deficiency": 3,
    "ADIPOQ-related_disorder": 5,
    "not_provided|ADIPOQ-related_disorder": 1,
    "3MC_syndrome_1": 53,
    "MASP1-related_disorder": 12,
    "not_provided|MASP1-related_disorder": 1,
    "Inborn_genetic_diseases|MASP1-related_disorder": 2,
    "not_provided|3MC_syndrome_1|MASP1-related_disorder": 1,
    "3MC_syndrome_1|MASP1-related_disorder|not_provided": 4,
    "not_provided|3MC_syndrome_1": 17,
    "Inborn_genetic_diseases|3MC_syndrome_1": 4,
    "3MC_syndrome_1|not_provided": 14,
    "Hypertrophic_cardiomyopathy|not_provided|Inborn_genetic_diseases": 2,
    "3MC_syndrome_1|not_specified": 1,
    "3MC_syndrome_1|MASP1-related_disorder": 1,
    "3MC_syndrome_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|3MC_syndrome_1": 5,
    "MASP1-related_disorder|not_provided": 2,
    "MASP1-related_disorder|3MC_syndrome_1": 3,
    "MASP1-related_disorder|not_provided|3MC_syndrome_1": 1,
    "not_provided|3MC_syndrome_1|Inborn_genetic_diseases": 1,
    "3MC_syndrome_1|Inborn_genetic_diseases": 5,
    "MASP1-related_disorder|3MC_syndrome_1|not_provided": 1,
    "3MC_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|3MC_syndrome_1|Monogenic_hearing_loss": 1,
    "not_provided|MASP1-related_disorder|not_specified|3MC_syndrome_1|Inborn_genetic_diseases": 1,
    "MASP1-related_disorder|not_specified|Inborn_genetic_diseases|3MC_syndrome_1": 1,
    "not_provided|MASP1-related_disorder|3MC_syndrome_1": 2,
    "LPP-related_disorder": 7,
    "Acute_myeloid_leukemia|not_specified": 2,
    "Acute_myeloid_leukemia|LPP-related_disorder": 1,
    "not_specified|LPP-related_disorder": 1,
    "LPP-related_disorder|not_provided": 5,
    "Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Premature_ovarian_failure_21": 1,
    "TP63-Related_Spectrum_Disorders|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 14,
    "not_provided|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 3,
    "not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 2,
    "TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8": 3,
    "Orofacial_cleft_8|TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 3,
    "Furrowed_tongue": 1,
    "TP63-Related_Spectrum_Disorders|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Premature_ovarian_failure_21|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|Limb-mammary_syndrome|not_provided": 1,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|TP63-related_disorder|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders": 363,
    "TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|ADULT_syndrome": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders|Orofacial_cleft_8": 14,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "TP63-Related_Spectrum_Disorders|not_specified": 2,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|ADULT_syndrome|Premature_ovarian_failure_21|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "TP63-related_disorder|TP63-Related_Spectrum_Disorders": 5,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Orofacial_cleft_8|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders": 1,
    "TP63-related_disorder": 10,
    "TP63-Related_Spectrum_Disorders|Premature_ovarian_failure_21|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Split_hand-foot_malformation_4|ADULT_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|not_provided|TP63-related_disorder": 1,
    "Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Premature_ovarian_failure_21|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Limb-mammary_syndrome": 22,
    "TP63-related_disorder|TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8": 1,
    "Rapp-Hodgkin_syndrome|ADULT_syndrome|Limb-mammary_syndrome|Orofacial_cleft_8|Split_hand-foot_malformation_4|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|not_specified|not_provided|TP63-Related_Spectrum_Disorders": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders|Rapp-Hodgkin_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|ADULT_syndrome|Split_hand-foot_malformation_4|Premature_ovarian_failure_21": 1,
    "TP63-Related_Spectrum_Disorders|not_provided": 7,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Split_hand-foot_malformation_4|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|ADULT_syndrome|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Premature_ovarian_failure_21|TP63-Related_Spectrum_Disorders": 1,
    "Limb-mammary_syndrome|Orofacial_cleft_8|ADULT_syndrome|Split_hand-foot_malformation_4|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Premature_ovarian_failure_21|Rapp-Hodgkin_syndrome|TP63-related_disorder|not_provided|TP63-Related_Spectrum_Disorders": 1,
    "Premature_ovarian_failure_21|Premature_ovarian_insufficiency": 4,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 14,
    "not_specified|TP63-Related_Spectrum_Disorders": 1,
    "not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 2,
    "ADULT_syndrome": 1,
    "ADULT_syndrome|Rapp-Hodgkin_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Orofacial_cleft_8|Premature_ovarian_failure_21|Limb-mammary_syndrome|Split_hand-foot_malformation_4|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders": 1,
    "Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Split_hand-foot_malformation_4|Limb-mammary_syndrome|ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "TP63-related_disorder|not_provided|Inborn_genetic_diseases|TP63-Related_Spectrum_Disorders": 1,
    "Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders|not_specified": 1,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders": 2,
    "TP63-Related_Spectrum_Disorders|Inborn_genetic_diseases": 4,
    "not_provided|TP63-Related_Spectrum_Disorders": 8,
    "TP63-Related_Spectrum_Disorders|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Premature_ovarian_failure_21|ADULT_syndrome|Split_hand-foot_malformation_4|Inborn_genetic_diseases": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome": 1,
    "Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "Split_hand-foot_malformation_4": 5,
    "Ankyloblepharon_filiforme_adnatum-cleft_palate_syndrome": 1,
    "Inborn_genetic_diseases|TP63-related_disorder": 2,
    "not_specified|Inborn_genetic_diseases|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome": 1,
    "TP63-Related_Spectrum_Disorders|TP63-related_disorder": 4,
    "Prostate_cancer|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|not_provided|TP63-related_disorder|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders": 2,
    "Orofacial_cleft_8|TP63-Related_Spectrum_Disorders|not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "TP63-Related_Spectrum_Disorders|not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|TP63-related_disorder": 1,
    "Orofacial_cleft_8|Rapp-Hodgkin_syndrome|Limb-mammary_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Premature_ovarian_failure_21|Split_hand-foot_malformation_4|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|not_provided": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|not_provided|TP63-Related_Spectrum_Disorders": 1,
    "not_provided|ADULT_syndrome|TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|not_provided": 2,
    "ADULT_syndrome|TP63-Related_Spectrum_Disorders": 2,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome": 1,
    "Orofacial_cleft_8": 1,
    "Rapp-Hodgkin_syndrome": 7,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|not_specified|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders": 17,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 8,
    "TP63-related_disorder|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "TP63-Related_Spectrum_Disorders|not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome": 1,
    "TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Split_hand-foot_malformation_4|not_provided": 1,
    "not_provided|TP63-related_disorder|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Split_hand-foot_malformation_4|ADULT_syndrome|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|TP63-Related_Spectrum_Disorders|not_provided": 1,
    "ADULT_syndrome|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 1,
    "not_provided|ADULT_syndrome": 1,
    "not_provided|TP63-related_disorder": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|not_provided": 1,
    "not_provided|TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Split_hand-foot_malformation_4|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|ADULT_syndrome|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Premature_ovarian_failure_21|TP63-Related_Spectrum_Disorders|Inborn_genetic_diseases": 1,
    "Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders": 1,
    "ADULT_syndrome|Split_hand-foot_malformation_4|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 1,
    "Inborn_genetic_diseases|TP63-Related_Spectrum_Disorders": 5,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Orofacial_cleft_8": 1,
    "not_provided|TP63-Related_Spectrum_Disorders|TP63-related_disorder": 3,
    "ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Orofacial_cleft_8|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Premature_ovarian_failure_21|TP63-Related_Spectrum_Disorders": 1,
    "Limb-mammary_syndrome": 2,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Premature_ovarian_failure_21|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Limb-mammary_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders": 1,
    "ADULT_syndrome|Split_hand-foot_malformation_4|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Orofacial_cleft_8|Rapp-Hodgkin_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "not_provided|TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Premature_ovarian_failure_21": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|ADULT_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-related_disorder": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Premature_ovarian_failure_21": 1,
    "TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Premature_ovarian_failure_21|Split_hand-foot_malformation_4|ADULT_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome": 1,
    "TP63-related_ectodermal_dysplasia": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Limb-mammary_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Premature_ovarian_failure_21": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Premature_ovarian_failure_21|Orofacial_cleft_8": 1,
    "TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Premature_ovarian_failure_21|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome": 1,
    "TP63-Related_Spectrum_Disorders|not_provided|Inborn_genetic_diseases|Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 1,
    "Split_hand-foot_malformation_4|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Orofacial_cleft_8|Rapp-Hodgkin_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|TP63-Related_Spectrum_Disorders|not_specified|not_provided": 1,
    "ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Premature_ovarian_failure_21|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_provided|TP63-related_disorder": 1,
    "ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|not_provided|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Premature_ovarian_failure_21|Split_hand-foot_malformation_4|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8": 1,
    "not_specified|TP63-Related_Spectrum_Disorders|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|not_provided": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Split_hand-foot_malformation_4|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Premature_ovarian_failure_21": 1,
    "not_provided|TP63-Related_Spectrum_Disorders|TP63-related_disorder|ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Orofacial_cleft_8": 1,
    "TP63-Related_Spectrum_Disorders|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|ADULT_syndrome": 1,
    "TP63-related_disorder|ADULT_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome": 2,
    "not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|not_specified|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 1,
    "Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome": 3,
    "ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Premature_ovarian_failure_21|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Limb-mammary_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome": 1,
    "Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Orofacial_cleft_8|Premature_ovarian_failure_21": 1,
    "Premature_ovarian_failure_21": 1,
    "TP63-Related_Spectrum_Disorders|TP63-related_disorder|not_provided": 1,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders|TP63-related_disorder": 1,
    "TP63-related_disorder|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|ADULT_syndrome|Premature_ovarian_failure_21|Split_hand-foot_malformation_4|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "TP63-Related_Spectrum_Disorders|ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|not_provided": 1,
    "Split_hand-foot_malformation_4|ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Limb-mammary_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3": 1,
    "TP63-related_disorder|not_provided|TP63-Related_Spectrum_Disorders": 1,
    "ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Rapp-Hodgkin_syndrome|Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Limb-mammary_syndrome|Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders": 1,
    "Limb-mammary_syndrome|TP63-Related_Spectrum_Disorders": 1,
    "ADULT_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Rapp-Hodgkin_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Premature_ovarian_failure_21|TP63-Related_Spectrum_Disorders": 1,
    "TP63-related_ectodermal_dysplasia_spectrum_with_limb_and_orofacial_malformations": 1,
    "Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Inborn_genetic_diseases|TP63-Related_Spectrum_Disorders": 1,
    "ADULT_syndrome|Rapp-Hodgkin_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Premature_ovarian_failure_21|Limb-mammary_syndrome|Split_hand-foot_malformation_4|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders|Inborn_genetic_diseases": 1,
    "not_provided|Limb-mammary_syndrome": 2,
    "ADULT_syndrome|Rapp-Hodgkin_syndrome|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|Split_hand-foot_malformation_4|TP63-Related_Spectrum_Disorders": 1,
    "Inborn_genetic_diseases|TP63-related_disorder|TP63-Related_Spectrum_Disorders": 1,
    "not_specified|not_provided|ADULT_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Split_hand-foot_malformation_4|Orofacial_cleft_8|Rapp-Hodgkin_syndrome": 1,
    "Orofacial_cleft_8|Ankyloblepharon-ectodermal_defects-cleft_lip/palate_syndrome|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Limb-mammary_syndrome|ADULT_syndrome|Rapp-Hodgkin_syndrome|Split_hand-foot_malformation_4|Premature_ovarian_failure_21|TP63-Related_Spectrum_Disorders": 1,
    "Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|Orofacial_cleft_8|not_provided|TP63-Related_Spectrum_Disorders|not_specified": 1,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|TP63-Related_Spectrum_Disorders|Ectrodactyly": 5,
    "not_provided|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders": 2,
    "TP63-Related_Spectrum_Disorders|Orofacial_cleft_8|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|not_provided": 3,
    "not_provided|Ectrodactyly|_ectodermal_dysplasia|_and_cleft_lip-palate_syndrome_3|TP63-Related_Spectrum_Disorders|Orofacial_cleft_8": 1,
    "TP63-Related_Spectrum_Disorders|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Ectrodactyly": 1,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|TP63-Related_Spectrum_Disorders|Ectrodactyly|not_provided": 1,
    "TP63-Related_Spectrum_Disorders|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|not_provided|Ectrodactyly": 1,
    "not_provided|Ectrodactyly|TP63-Related_Spectrum_Disorders|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "Ectrodactyly|not_provided|TP63-Related_Spectrum_Disorders|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "not_provided|P3H2-related_disorder": 9,
    "Myopia|_high|_with_cataract_and_vitreoretinal_degeneration": 6,
    "P3H2-related_disorder|not_provided": 5,
    "Myopia": 1,
    "not_provided|P3H2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Myopia|_high|_with_cataract_and_vitreoretinal_degeneration": 8,
    "Myopia|_high|_with_cataract_and_vitreoretinal_degeneration|Retinitis_pigmentosa|not_provided": 1,
    "Myopia|_high|_with_cataract_and_vitreoretinal_degeneration|not_provided": 3,
    "Rare_isolated_myopia|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Myopia|_high|_with_cataract_and_vitreoretinal_degeneration": 1,
    "Inborn_genetic_diseases|not_provided|P3H2-related_disorder": 1,
    "P3H2-related_disorder": 2,
    "CLDN1-related_disorder": 13,
    "not_provided|CLDN1-related_disorder|Inborn_genetic_diseases": 1,
    "Neonatal_ichthyosis-sclerosing_cholangitis_syndrome": 7,
    "Neonatal_ichthyosis-sclerosing_cholangitis_syndrome|not_provided|not_specified": 1,
    "not_provided|CLDN1-related_disorder": 2,
    "Neonatal_ichthyosis-sclerosing_cholangitis_syndrome|not_provided": 1,
    "CLDN1-related_disorder|not_provided": 1,
    "CLDN1-related_disorder|Neonatal_ichthyosis-sclerosing_cholangitis_syndrome|not_provided": 1,
    "Primary_hypomagnesemia": 105,
    "not_provided|Primary_hypomagnesemia": 21,
    "CLDN16-related_disorder|Primary_hypomagnesemia|not_provided": 1,
    "not_provided|Primary_hypomagnesemia|Inborn_genetic_diseases": 2,
    "not_specified|Primary_hypomagnesemia|not_provided": 1,
    "not_provided|not_specified|Primary_hypomagnesemia": 1,
    "Inborn_genetic_diseases|Primary_hypomagnesemia|not_provided": 3,
    "CLDN16-related_disorder|Primary_hypomagnesemia": 1,
    "Primary_hypomagnesemia|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_hypomagnesemia": 2,
    "CLDN16-related_disorder": 2,
    "Primary_hypomagnesemia|not_provided": 16,
    "not_provided|Primary_hypomagnesemia|not_specified": 1,
    "Primary_hypomagnesemia|Thrombocytopenia_5": 1,
    "Primary_hypomagnesemia|Inborn_genetic_diseases|not_provided": 1,
    "Nephrocalcinosis|Nephrolithiasis|Primary_hypomagnesemia": 1,
    "not_provided|Primary_hypomagnesemia|CLDN16-related_disorder": 1,
    "HYPERCALCIURIA|_CHILDHOOD|_SELF-LIMITING": 1,
    "High_myopia|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_44|not_provided|not_specified": 2,
    "CCDC50-related_disorder": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_44": 6,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_44|Hearing_impairment": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|not_specified": 1,
    "CCDC50-related_disorder|not_specified|not_provided": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_44|not_provided": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_44|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_44|not_specified": 5,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_44": 1,
    "CCDC50-related_disorder|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_44|not_specified|not_provided": 1,
    "not_provided|CCDC50-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_47": 8,
    "not_provided|FGF12-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_47": 3,
    "Developmental_and_epileptic_encephalopathy|_47|not_provided": 4,
    "FGF12-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_47|Seizure|Early_onset_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_47|not_provided|FGF12-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|FGF12-related_disorder": 1,
    "FGF12-related_disorder|not_provided": 1,
    "FGF12-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|ATP13A4-related_disorder": 5,
    "not_provided|ATP13A4-related_disorder|not_specified": 2,
    "ATP13A4-related_disorder": 12,
    "not_provided|Central_core_myopathy|ATP13A4-related_disorder": 1,
    "ATP13A4-related_disorder|not_provided": 1,
    "Autosomal_dominant_optic_atrophy_classic_form": 87,
    "not_specified|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|OPA1-related_disorder": 1,
    "OPA1-related_disorder|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy": 1,
    "not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 5,
    "Autosomal_dominant_optic_atrophy_classic_form|not_provided": 19,
    "Autosomal_dominant_optic_atrophy_classic_form|not_provided|not_specified": 5,
    "not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|OPA1-related_disorder": 1,
    "Abortive_cerebellar_ataxia|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_specified|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|OPA1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "OPA1-related_disorder|not_provided|not_specified|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|Abortive_cerebellar_ataxia|not_specified|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Optic_atrophy|Progressive_proximal_muscle_weakness|Ptosis|EMG_abnormality|EMG:_myopathic_abnormalities|Muscle_weakness|Elevated_circulating_creatine_kinase_concentration|EMG:_myotonic_runs|Hypomimic_face|Hepatic_steatosis": 1,
    "not_provided|Optic_atrophy|Autosomal_dominant_optic_atrophy_classic_form|OPA1-related_disorder|Retinal_dystrophy": 1,
    "OPA1-related_disorder|not_provided": 11,
    "not_provided|Autosomal_dominant_optic_atrophy_classic_form": 25,
    "OPA1-related_disorder": 16,
    "Autosomal_dominant_optic_atrophy_classic_form|not_specified|OPA1-related_disorder|not_provided": 1,
    "not_provided|Abortive_cerebellar_ataxia": 2,
    "not_specified|OPA1-related_disorder|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Abortive_cerebellar_ataxia": 10,
    "Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 18,
    "Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|not_specified|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_provided|Abortive_cerebellar_ataxia": 1,
    "not_specified|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "OPA1-related_optic_atrophy_with_or_without_extraocular_features|not_provided": 2,
    "not_specified|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 6,
    "not_provided|not_specified|Autosomal_dominant_optic_atrophy_classic_form": 2,
    "Autosomal_dominant_optic_atrophy_classic_form|OPA1-related_disorder|not_provided": 2,
    "not_provided|OPA1-related_disorder": 9,
    "not_provided|OPA1-related_disorder|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "not_provided|OPA1-related_disorder|not_specified": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_optic_atrophy_classic_form|Glaucoma|_normal_tension|_susceptibility_to|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Abortive_cerebellar_ataxia|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "not_specified|not_provided|OPA1-related_disorder": 1,
    "Osteoporosis|Mildly_elevated_creatine_kinase|Limb_pain|Myotonia": 1,
    "not_provided|Optic_atrophy|Retinal_dystrophy": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_optic_atrophy_classic_form|Stargardt_disease|Optic_atrophy": 1,
    "Optic_atrophy|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 3,
    "not_provided|Autosomal_dominant_optic_atrophy_classic_form|Inborn_genetic_diseases": 1,
    "Abortive_cerebellar_ataxia|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_provided|Inborn_genetic_diseases": 1,
    "Abnormal_brain_morphology|not_provided": 2,
    "Retinal_dystrophy|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Ocular_impairment|not_provided": 1,
    "Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_specified|not_provided|Abortive_cerebellar_ataxia": 1,
    "Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Glaucoma|_normal_tension|_susceptibility_to|Autosomal_dominant_optic_atrophy_classic_form|Abortive_cerebellar_ataxia|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)": 1,
    "Neurodevelopmental_disorder|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy|not_provided": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy": 3,
    "Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|not_provided": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "OPA1-related_disorder|not_specified|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_optic_atrophy_with_or_without_extraocular_features|Optic_atrophy|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|not_provided|not_specified": 1,
    "Optic_atrophy|Autosomal_dominant_optic_atrophy_classic_form": 3,
    "Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Abortive_cerebellar_ataxia|Inborn_genetic_diseases|Optic_nerve_hypoplasia|not_specified|Optic_atrophy|not_provided": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|not_specified|not_provided": 3,
    "not_provided|Abortive_cerebellar_ataxia|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "Mitochondrial_disease|not_provided": 13,
    "Abortive_cerebellar_ataxia|not_provided": 4,
    "Autosomal_dominant_optic_atrophy_classic_form|Abortive_cerebellar_ataxia|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|not_provided": 1,
    "Mitochondrial_disease|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Optic_atrophy|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|Optic_atrophy|not_provided|Centronuclear_myopathy|Mitochondrial_disease|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "OPA1-related_disorder|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "not_specified|not_provided|Optic_atrophy": 2,
    "OPA1-related_disorder|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|Inborn_genetic_diseases": 1,
    "Abortive_cerebellar_ataxia|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)": 2,
    "Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_provided|not_specified|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "not_provided|Mitochondrial_disease|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy": 1,
    "OPA1-related_disorder|Optic_atrophy|not_provided": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy|not_provided": 1,
    "not_specified|OPA1-related_disorder|not_provided": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|not_specified|Abortive_cerebellar_ataxia": 1,
    "OPA1-related_disorder|not_provided|Abortive_cerebellar_ataxia|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy": 1,
    "OPA1-related_disorder|not_provided|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy": 1,
    "OPA1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Abortive_cerebellar_ataxia|Glaucoma|_normal_tension|_susceptibility_to|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "not_provided|Optic_Atrophy|_Dominant|not_specified|Optic_atrophy|Inborn_genetic_diseases": 1,
    "Optic_atrophy|not_specified|not_provided|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "not_provided|Autosomal_dominant_optic_atrophy_classic_form|Inborn_genetic_diseases|OPA1-related_disorder": 1,
    "not_provided|Abortive_cerebellar_ataxia|Glaucoma|_normal_tension|_susceptibility_to|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)": 1,
    "not_provided|Abortive_cerebellar_ataxia|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Optic_atrophy": 2,
    "Glaucoma|_normal_tension|_susceptibility_to|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Autosomal_dominant_optic_atrophy_classic_form|Abortive_cerebellar_ataxia|not_provided": 1,
    "not_provided|OPA1-related_disorder|Optic_atrophy|Autosomal_dominant_optic_atrophy_classic_form": 1,
    "Dominant_hereditary_optic_atrophy": 1,
    "OPA1-related_disorder|Glaucoma|_normal_tension|_susceptibility_to|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)|Autosomal_dominant_optic_atrophy_classic_form|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|Abortive_cerebellar_ataxia|Optic_atrophy|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Mitochondrial_disease|3-Methylglutaconic_aciduria_type_3|Tip-toe_gait|See_cases": 1,
    "Autosomal_dominant_optic_atrophy_classic_form|not_provided|Optic_atrophy_with_or_without_deafness|_ophthalmoplegia|_myopathy|_ataxia|_and_neuropathy|not_specified": 1,
    "See_cases|Optic_atrophy": 1,
    "not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_14_(cardioencephalomyopathic_type)": 1,
    "Optic_Atrophy|_Dominant": 1,
    "not_provided|ATP13A3-related_disorder": 6,
    "not_provided|Pulmonary_hypertension|_primary|_autosomal_recessive|Pulmonary_arterial_hypertension": 1,
    "ATP13A3-related_disorder": 7,
    "ATP13A3-related_disorder|not_provided|not_specified": 1,
    "ATP13A3-related_disorder|not_provided": 5,
    "Pulmonary_hypertension|_primary|_autosomal_recessive|Pulmonary_arterial_hypertension": 4,
    "Pulmonary_hypertension|_primary|_autosomal_recessive|not_provided|not_specified": 1,
    "Pulmonary_hypertension|_primary|_autosomal_recessive": 2,
    "Pulmonary_hypertension|_primary|_autosomal_recessive|not_specified": 1,
    "not_provided|ATP13A3-related_disorder|not_specified": 1,
    "ATP13A3-related_disorder|not_specified|not_provided": 1,
    "APOD-related_disorder": 2,
    "not_provided|APOD-related_disorder": 1,
    "MUC4-related_disorder": 3,
    "MUC4-related_condition": 1,
    "TNK2-related_disorder": 11,
    "not_specified|not_provided|Parkinson_disease": 1,
    "TNK2-related_disorder|not_provided": 7,
    "Parkinson_disease|Autosomal_recessive_infantile_epilepsy|TNK2-related_disorder|not_provided|Infantile_epilepsy": 1,
    "not_provided|Abnormality_of_neuronal_migration": 6,
    "TNK2-associated_Epilepsy_syndrome|not_specified|not_provided": 1,
    "not_provided|TNK2-related_disorder": 1,
    "not_provided|TFRC-related_combined_immunodeficiency": 6,
    "TFRC-related_disorder|not_provided": 3,
    "TFRC-related_combined_immunodeficiency|not_provided|not_specified": 5,
    "TFRC-related_combined_immunodeficiency|not_specified|not_provided": 3,
    "not_provided|TFRC-related_disorder": 4,
    "TFRC-related_combined_immunodeficiency": 2,
    "TFRC-related_disorder": 2,
    "TFRC-related_combined_immunodeficiency|not_provided": 1,
    "TFRC-related_disorder|TFRC-related_combined_immunodeficiency|Combined_immunodeficiency|not_provided": 1,
    "SLC51A-related_disorder": 38,
    "not_specified|SLC51A-related_disorder": 2,
    "not_specified|Cholestasis|_progressive_familial_intrahepatic|_6": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_6": 2,
    "SLC51A-related_disorder|not_specified": 2,
    "Spondylometaphyseal_dysplasia-cone-rod_dystrophy_syndrome|not_provided": 3,
    "not_provided|PCYT1A-related_disorder": 3,
    "not_provided|Lipodystrophy|_congenital_generalized|_type_5": 2,
    "not_provided|Spondylometaphyseal_dysplasia-cone-rod_dystrophy_syndrome": 6,
    "Spondylometaphyseal_dysplasia-cone-rod_dystrophy_syndrome": 6,
    "Inborn_genetic_diseases|not_provided|PCYT1A-related_disorder": 1,
    "Lipodystrophy|_congenital_generalized|_type_5": 2,
    "not_provided|Spondylometaphyseal_dysplasia-cone-rod_dystrophy_syndrome|Inborn_genetic_diseases": 1,
    "PCYT1A-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Spondylometaphyseal_dysplasia-cone-rod_dystrophy_syndrome": 1,
    "Lipodystrophy|_congenital_generalized|_type_5|Spondylometaphyseal_dysplasia-cone-rod_dystrophy_syndrome": 1,
    "DYNLT2B-related_disorder|not_provided": 2,
    "not_provided|DYNLT2B-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_17_with_or_without_polydactyly|Asphyxiating_thoracic_dystrophy_3": 1,
    "Short-rib_thoracic_dysplasia_17_with_or_without_polydactyly|not_provided": 2,
    "Short-rib_thoracic_dysplasia_17_with_or_without_polydactyly": 4,
    "DYNLT2B-related_disorder": 1,
    "not_provided|RNF168-related_disorder": 2,
    "RNF168-related_disorder": 1,
    "RIDDLE_syndrome": 8,
    "not_provided|RIDDLE_syndrome": 6,
    "RIDDLE_syndrome|RNF168-related_disorder|not_provided": 1,
    "RIDDLE_syndrome|not_provided|RNF168-related_disorder|not_specified": 1,
    "RIDDLE_syndrome|not_specified|not_provided": 1,
    "RNF168-related_disorder|not_provided": 6,
    "RIDDLE_syndrome|not_provided": 7,
    "Inborn_genetic_diseases|RIDDLE_syndrome|not_provided": 1,
    "RNF168-related_disorder|not_specified|not_provided|RIDDLE_syndrome": 1,
    "RNF168-related_disorder|RIDDLE_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|RIDDLE_syndrome": 1,
    "Seizures|_early-onset|_with_neurodegeneration_and_brain_calcifications": 14,
    "Seizures|_early-onset|_with_neurodegeneration_and_brain_calcifications|not_provided|Inborn_genetic_diseases": 1,
    "Seizures|_early-onset|_with_neurodegeneration_and_brain_calcifications|Inborn_genetic_diseases|not_provided": 1,
    "Seizures|_early-onset|_with_neurodegeneration_and_brain_calcifications|Inborn_genetic_diseases": 2,
    "not_provided|Seizures|_early-onset|_with_neurodegeneration_and_brain_calcifications": 2,
    "NRROS-related_disorder": 2,
    "not_provided|Obesity_due_to_CEP19_deficiency": 2,
    "not_provided|CEP19-related_disorder": 1,
    "Obesity_due_to_CEP19_deficiency|not_provided": 1,
    "PAK2-related_disorder": 3,
    "Knobloch_syndrome_2": 4,
    "Knobloch_syndrome": 70,
    "DLG1-related_disorder": 21,
    "DLG1-related_disorder|not_provided": 1,
    "not_specified|DLG1-related_disorder": 1,
    "BDH1-related_disorder": 7,
    "BDH1-related_disorder|not_provided": 2,
    "RUBCN-related_disorder": 8,
    "Autosomal_recessive_spinocerebellar_ataxia_15": 9,
    "RUBCN-related_disorder|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_15": 1,
    "not_provided|not_specified|Autosomal_recessive_spinocerebellar_ataxia_15": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_15|not_provided": 2,
    "Elbow_flexion_contracture|Global_developmental_delay|Intellectual_disability|Knee_flexion_contracture|Cerebral_hypomyelination|Nystagmus|Hypotonia|not_provided|Autosomal_recessive_spinocerebellar_ataxia_15": 1,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_15": 1,
    "not_provided|RUBCN-related_disorder": 2,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_15|not_provided": 1,
    "not_provided|Elbow_flexion_contracture|Global_developmental_delay|Intellectual_disability|Knee_flexion_contracture|Cerebral_hypomyelination|Nystagmus|Hypotonia|Autosomal_recessive_spinocerebellar_ataxia_15": 1,
    "LRCH3-related_disorder": 21,
    "Diamond-Blackfan_anemia_5": 95,
    "Diamond-Blackfan_anemia_5|RPL35A-related_disorder|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_5|RPL35A-related_disorder|Diamond-Blackfan_anemia|not_specified|not_provided": 1,
    "RPL35A-related_disorder|Diamond-Blackfan_anemia_5": 2,
    "not_provided|Diamond-Blackfan_anemia_5": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_5": 3,
    "Diamond-Blackfan_anemia_5|Diamond-Blackfan_anemia|not_provided": 2,
    "Diamond-Blackfan_anemia_5|RPL35A-related_disorder": 1,
    "Diamond-Blackfan_anemia_5|not_provided": 1,
    "not_specified|Diamond-Blackfan_anemia_5|RPL35A-related_disorder": 1,
    "ZNF141-related_disorder": 13,
    "not_specified|ZNF141-related_disorder": 2,
    "not_specified|ZNF141-related_disorder|not_provided": 1,
    "ZNF141-related_disorder|not_specified": 1,
    "not_provided|ZNF141-related_disorder": 2,
    "Polydactyly|_postaxial|_type_A6": 1,
    "Intellectual_disability|_autosomal_recessive_53|Seizure": 1,
    "Intellectual_disability|_autosomal_recessive_53": 710,
    "Intellectual_disability|_autosomal_recessive_53|not_provided": 50,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_53": 16,
    "Intellectual_disability|_autosomal_recessive_53|Inborn_genetic_diseases": 49,
    "Intellectual_disability|_autosomal_recessive_53|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_53|not_provided": 5,
    "not_provided|Intellectual_disability|_autosomal_recessive_53": 41,
    "Emm-null_phenotype": 3,
    "PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53": 9,
    "not_provided|Intellectual_disability|_autosomal_recessive_53|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_recessive_53|PIGG-related_disorder|Inborn_genetic_diseases": 1,
    "Emm-null_phenotype|Intellectual_disability|_autosomal_recessive_53": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_53": 1,
    "PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53|Inborn_genetic_diseases|not_provided": 1,
    "PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53|not_provided": 3,
    "Intellectual_disability|_autosomal_recessive_53|Inborn_genetic_diseases|not_provided": 5,
    "Intellectual_disability|_autosomal_recessive_53|not_provided|not_specified|See_cases": 1,
    "Intellectual_disability|_autosomal_recessive_53|not_provided|PIGG-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_53|not_specified": 1,
    "not_provided|PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_53|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_53|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Intellectual_disability|_autosomal_recessive_53|PIGG-related_disorder": 3,
    "BLOOD_GROUP|_EMM_SYSTEM|Intellectual_disability|_autosomal_recessive_53|not_provided|Inborn_genetic_diseases": 1,
    "PIGG-related_disorder": 1,
    "PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_53|PIGG-related_disorder|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_53|Hyperphosphatasia_with_intellectual_disability_syndrome_1": 1,
    "PIGG-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_53|not_provided": 1,
    "PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_53|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|BLOOD_GROUP|_EMM_SYSTEM|Intellectual_disability|_autosomal_recessive_53|PIGG-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_53|not_provided|Emm-null_phenotype": 1,
    "PIGG-related_disorder|Intellectual_disability|_autosomal_recessive_53|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_53|not_provided|PIGG-related_disorder": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa_40": 1,
    "PDE6B-related_disorder|not_provided": 8,
    "Retinitis_pigmentosa|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2": 14,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa": 15,
    "not_specified|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa": 2,
    "not_provided|not_specified|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Retinitis_pigmentosa_40|not_provided": 7,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa": 10,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_40": 3,
    "Retinitis_pigmentosa_40": 29,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|PDE6B-related_disorder": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2": 2,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa_40|not_provided": 1,
    "Congenital_stationary_night_blindness|not_provided": 10,
    "not_provided|Retinitis_pigmentosa_40|Retinitis_pigmentosa|PDE6B-related_disorder|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|not_specified": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_40|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_40": 2,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa|High_myopia": 1,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Retinitis_pigmentosa_40|Macular_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 2,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa|not_specified|not_provided": 1,
    "PDE6B-related_disorder|Retinal_dystrophy|not_provided": 4,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 4,
    "not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 15,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|See_cases": 1,
    "not_provided|Retinitis_pigmentosa_40|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 17,
    "Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2": 2,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|Retinitis_pigmentosa|not_specified": 2,
    "Retinitis_pigmentosa_40|Leber_congenital_amaurosis|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_40": 2,
    "not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2|not_specified": 1,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 3,
    "Retinitis_pigmentosa_40|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_40|not_specified": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_40|not_provided": 1,
    "PDE6B-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_40": 1,
    "PDE6B-related_disorder": 2,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_40": 3,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Congenital_Stationary_Night_Blindness|_Dominant|Retinitis_Pigmentosa|_Recessive|not_specified": 1,
    "Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|Inborn_genetic_diseases|PDE6B-related_disorder": 1,
    "Retinitis_pigmentosa_40|Retinal_dystrophy": 2,
    "not_specified|PDE6B-related_disorder|not_provided": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided|Retinitis_pigmentosa": 4,
    "Retinitis_pigmentosa_40|Autosomal_recessive_retinitis_pigmentosa|Congenital_Stationary_Night_Blindness|_Dominant|not_provided|PDE6B-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_40|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa_40|Retinal_dystrophy": 1,
    "Progressive_cone_dystrophy_(without_rod_involvement)|Rod-cone_dystrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_40|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "PDE6B-related_disorder|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_40|Retinitis_pigmentosa": 1,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa|not_provided": 3,
    "not_provided|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2": 2,
    "Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa_40|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_40|not_provided|Retinal_dystrophy": 2,
    "not_provided|Retinitis_pigmentosa_40|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_40|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|PDE6B-related_disorder|Retinitis_pigmentosa_40|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_40": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_40|Retinal_dystrophy": 1,
    "not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa_40": 2,
    "not_provided|PDE6B-related_disorder": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_autosomal_dominant_2": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "Retinitis_pigmentosa_40|PDE6B-related_disorder|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|Congenital_stationary_night_blindness_autosomal_dominant_2": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_40": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_40|Congenital_stationary_night_blindness_autosomal_dominant_2|not_provided": 1,
    "not_provided|PDE6B-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Retinitis_pigmentosa|Retinitis_pigmentosa_40|not_provided|Retinal_dystrophy": 1,
    "Congenital_Stationary_Night_Blindness|_Dominant|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinitis_pigmentosa_40|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_autosomal_dominant_2|PDE6B-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinitis_pigmentosa_40|Retinitis_pigmentosa": 1,
    "Congenital_Stationary_Night_Blindness|_Dominant|not_provided|Retinitis_Pigmentosa|_Recessive": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_63": 1,
    "CPLX1-related_disorder": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_63|4p_partial_monosomy_syndrome": 1,
    "not_provided|CPLX1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_63|Abnormal_brain_morphology": 1,
    "Developmental_and_epileptic_encephalopathy|_63": 3,
    "Developmental_and_epileptic_encephalopathy|_63|not_provided": 2,
    "CPLX1-related_disorder|not_provided": 3,
    "Primary_ciliary_dyskinesia_18|not_provided": 9,
    "TMEM175-related_disorder": 2,
    "not_provided|TMEM175-related_disorder": 1,
    "DGKQ-related_disorder": 13,
    "DGKQ-related_disorder|not_provided": 1,
    "not_specified|DGKQ-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1": 4,
    "Mucopolysaccharidosis_type_1": 1069,
    "Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome": 17,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome": 22,
    "not_provided|Mucopolysaccharidosis_type_1": 60,
    "Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis_type_1": 3,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_1|not_provided": 7,
    "Mucopolysaccharidosis|_MPS-I-H/S": 20,
    "Mucopolysaccharidosis_type_1|not_specified|not_provided": 8,
    "Mucopolysaccharidosis_type_1|Inborn_genetic_diseases|not_provided": 5,
    "Hurler_syndrome": 69,
    "Mucopolysaccharidosis|_MPS-I-S": 3,
    "IDUA-related_disorder|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome": 14,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_1": 22,
    "Mucopolysaccharidosis_type_1|Inborn_genetic_diseases": 31,
    "not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis_type_1": 9,
    "Mucopolysaccharidosis_type_1|not_provided|not_specified|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S|Inborn_genetic_diseases|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis_type_1|not_provided": 65,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S|not_provided": 5,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 3,
    "See_cases|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 1,
    "Mucopolysaccharidosis_type_1|not_specified": 3,
    "not_provided|IDUA-related_disorder|Mucopolysaccharidosis_type_1|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 1,
    "not_provided|Mucopolysaccharidosis_type_1|Hurler_syndrome": 3,
    "not_provided|Mucopolysaccharidosis_type_1|Inborn_genetic_diseases": 3,
    "Hurler_syndrome|Mucopolysaccharidosis_type_1|not_provided": 5,
    "IDUA-related_disorder|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|not_provided|Interstitial_pneumonitis": 1,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|not_specified|not_provided|Nephrolithiasis|_calcium_oxalate": 1,
    "IDUA-related_disorder": 4,
    "Mucopolysaccharidosis_type_1|not_specified|not_provided|Hurler_syndrome": 2,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_1|not_specified|not_provided|Hurler_syndrome": 1,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 4,
    "Mucopolysaccharidosis_type_1|IDUA-related_disorder|not_provided": 1,
    "not_provided|Hurler_syndrome|Mucopolysaccharidosis_type_1": 4,
    "Mucopolysaccharidosis_type_1|not_specified|not_provided|Nephrolithiasis|_calcium_oxalate|Hurler_syndrome": 1,
    "Hereditary_disease|Mucopolysaccharidosis_type_1|not_specified|not_provided": 1,
    "Mucopolysaccharidosis_type_1|IDUA-related_disorder": 2,
    "Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 74,
    "Inborn_genetic_diseases|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 10,
    "Inborn_genetic_diseases|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia": 4,
    "not_specified|not_provided|Nephrolithiasis|_calcium_oxalate|SLC26A1-related_disorder": 1,
    "Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|not_provided": 16,
    "not_provided|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 13,
    "SLC26A1-related_disorder|Nephrolithiasis|_calcium_oxalate|not_provided": 1,
    "not_provided|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia": 10,
    "not_provided|Hurler_syndrome": 2,
    "Nephrolithiasis|_calcium_oxalate|not_provided|SLC26A1-related_disorder": 1,
    "Nephrolithiasis|_calcium_oxalate|not_provided": 21,
    "Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Inborn_genetic_diseases": 11,
    "not_provided|Nephrolithiasis|_calcium_oxalate": 7,
    "Hurler_syndrome|not_provided": 3,
    "Hurler_syndrome|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|not_provided": 1,
    "Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|not_provided": 3,
    "SLC26A1-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia": 1,
    "Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|not_provided|Inborn_genetic_diseases": 2,
    "Nephrolithiasis|_calcium_oxalate|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 1,
    "SLC26A1-related_disorder|not_provided": 5,
    "Nephrolithiasis|_calcium_oxalate|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Nephrolithiasis|_calcium_oxalate": 2,
    "not_provided|Inborn_genetic_diseases|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 7,
    "Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|not_provided|Hurler_syndrome": 1,
    "Inborn_genetic_diseases|SLC26A1-related_disorder": 1,
    "not_provided|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Inborn_genetic_diseases": 2,
    "not_provided|Hurler_syndrome|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia": 2,
    "not_provided|SLC26A1-related_disorder": 4,
    "Inborn_genetic_diseases|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|not_provided": 2,
    "Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Nephrolithiasis|_calcium_oxalate|not_provided": 1,
    "Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Inborn_genetic_diseases|not_provided": 7,
    "not_provided|Hyperoxaluria": 1,
    "Nephrolithiasis_susceptibility_caused_by_SLC26A1|not_provided": 2,
    "not_provided|Nephrolithiasis|_calcium_oxalate|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|SLC26A1-related_disorder": 1,
    "not_provided|Nephrolithiasis|_calcium_oxalate|SLC26A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Nephrolithiasis|_calcium_oxalate|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia": 1,
    "not_provided|SLC26A1-related_disorder|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 1,
    "Mucopolysaccharidosis|_MPS-I-H/S|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|Inborn_genetic_diseases|not_provided": 1,
    "Nephrolithiasis|_calcium_oxalate|Hypersulfaturia": 1,
    "Inborn_genetic_diseases|not_provided|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1": 1,
    "Nephrolithiasis|_calcium_oxalate|not_provided|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hypersulfaturia|SLC26A1-related_disorder": 1,
    "not_provided|Nephrolithiasis|_calcium_oxalate|Inborn_genetic_diseases": 1,
    "Hyperoxaluria|Nephrolithiasis|_calcium_oxalate|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Nephrolithiasis|_calcium_oxalate|SLC26A1-related_disorder": 1,
    "Nephrolithiasis_susceptibility_caused_by_SLC26A1|Inborn_genetic_diseases|not_provided": 1,
    "Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|Hurler_syndrome": 1,
    "not_provided|SLC26A1-related_disorder|Nephrolithiasis|_calcium_oxalate": 1,
    "not_provided|Hypersulfaturia|Nephrolithiasis_susceptibility_caused_by_SLC26A1|SLC26A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Disorder_of_lung": 1,
    "not_provided|SLC26A1-related_disorder|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|not_provided": 1,
    "not_specified|Mucopolysaccharidosis_type_1|not_provided": 3,
    "Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1|Hurler_syndrome": 1,
    "Mucopolysaccharidosis_type_1|not_provided|not_specified|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S": 3,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|not_provided|Mucopolysaccharidosis|_MPS-I-H/S|not_specified": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|not_provided": 3,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 7,
    "Hurler_syndrome|Mucopolysaccharidosis_type_1": 13,
    "Inborn_genetic_diseases|not_specified|not_provided|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis|_MPS-I-H/S|IDUA-related_disorder|Mucopolysaccharidosis_type_1": 1,
    "IDUA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Mucopolysaccharidosis_type_1|IDUA-related_disorder": 1,
    "Mucopolysaccharidosis_type_1|not_specified|Inborn_genetic_diseases|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Mucopolysaccharidosis_type_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|IDUA-related_disorder|Mucopolysaccharidosis_type_1": 1,
    "Hurler_syndrome|not_provided|Mucopolysaccharidosis_type_1": 1,
    "Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|not_provided|Mucopolysaccharidosis_type_1": 1,
    "not_provided|not_specified|Mucopolysaccharidosis_type_1": 5,
    "Mucopolysaccharidosis_type_1|not_specified|not_provided|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis_type_1|not_provided|not_specified|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Hurler_syndrome|Mucopolysaccharidosis_type_1|not_specified|Mucopolysaccharidosis|_MPS-I-H/S|not_provided|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis_type_1|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis_type_1": 2,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S": 3,
    "Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis_type_1": 2,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1|not_provided": 4,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|IDUA-related_disorder|not_provided": 1,
    "IDUA-related_disorder|not_specified|Mucopolysaccharidosis_type_1|not_provided": 1,
    "IDUA-related_disorder|Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "not_specified|Hurler_syndrome|Mucopolysaccharidosis_type_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome|not_specified": 2,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|not_specified|not_provided": 1,
    "IDUA-related_core_myopathy|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S": 1,
    "not_provided|IDUA_PSEUDODEFICIENCY|Mucopolysaccharidosis_type_1|Hurler_syndrome": 1,
    "Hurler_syndrome|Mucopolysaccharidosis_type_1|not_provided|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|not_provided": 1,
    "not_specified|not_provided|Hurler_syndrome|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|not_specified|Mucopolysaccharidosis_type_1": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-I-S|not_specified|Hurler_syndrome|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Hurler_syndrome|not_specified": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Inborn_genetic_diseases": 2,
    "Mucopolysaccharidosis_type_1|IDUA-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 1,
    "not_provided|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S": 2,
    "Mucopolysaccharidosis|_MPS-II": 1148,
    "not_provided|Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S": 1,
    "not_specified|Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|not_specified|not_provided": 1,
    "not_provided|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 3,
    "Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "IDUA-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis_type_1": 1,
    "not_provided|Hurler_syndrome|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hurler_syndrome": 1,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|not_provided": 1,
    "not_specified|not_provided|Mucopolysaccharidosis_type_1": 3,
    "not_provided|Mucopolysaccharidosis_type_1|not_specified": 2,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S": 5,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|IDUA-related_disorder|Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S|See_cases": 1,
    "Hurler_syndrome|Inborn_genetic_diseases|Mucopolysaccharidosis_type_1": 1,
    "Hurler_syndrome|IDUA-related_disorder|Mucopolysaccharidosis_type_1": 1,
    "Inborn_genetic_diseases|IDUA-related_disorder|Mucopolysaccharidosis_type_1|not_provided": 1,
    "Mucopolysaccharidosis_type_1|not_specified|IDUA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|IDUA-related_disorder|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis_type_1|not_specified|not_provided|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S": 2,
    "Mucopolysaccharidosis_type_1|not_provided|See_cases": 1,
    "Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 2,
    "not_provided|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis_type_1|not_specified|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "not_provided|Mucopolysaccharidosis_type_1|not_specified|Hurler_syndrome": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Mucopolysaccharidosis|_MPS-I-H/S|Hurler_syndrome": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 1,
    "not_specified|Mucopolysaccharidosis_type_1": 2,
    "not_specified|not_provided|Mucopolysaccharidosis_type_1|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Interstitial_pneumonitis": 1,
    "Mucopolysaccharidosis_type_1|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S|not_provided": 1,
    "Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "not_provided|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|IDUA-related_disorder": 1,
    "IDUA-related_disorder|Hurler_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-I-H/S|Mucopolysaccharidosis|_MPS-I-S|Hurler_syndrome|Mucopolysaccharidosis_type_1": 1,
    "Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-S": 1,
    "Mucopolysaccharidosis_type_1|Hurler_syndrome|Mucopolysaccharidosis|_MPS-I-H/S": 1,
    "Familial_hypokalemia-hypomagnesemia|Hurler_syndrome|Mucopolysaccharidosis_type_1": 1,
    "IDUA-related_disorder|Mucopolysaccharidosis_type_1": 1,
    "Mucopolysaccharidosis_type_1|not_provided|Hurler_syndrome|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "not_provided|FGFRL1-related_disorder": 8,
    "FGFRL1-related_disorder|not_provided": 11,
    "not_provided|Flexion_contracture": 2,
    "4p_partial_monosomy_syndrome|not_provided|FGFRL1-related_disorder": 1,
    "not_specified|FGFRL1-related_disorder|not_provided": 1,
    "not_provided|Congenital_diaphragmatic_hernia": 2,
    "FGFRL1-related_disorder": 3,
    "RNF212-related_disorder": 9,
    "Spermatogenic_failure_62": 2,
    "RECOMBINATION_RATE_QUANTITATIVE_TRAIT_LOCUS_1": 2,
    "Spermatogenic_failure_62|not_provided": 1,
    "Down_syndrome": 1,
    "not_provided|Hypotonia|_ataxia|_developmental_delay|_and_tooth_enamel_defect_syndrome": 2,
    "Hypotonia|_ataxia|_developmental_delay|_and_tooth_enamel_defect_syndrome": 12,
    "not_provided|CTBP1-related_disorder": 4,
    "Inborn_genetic_diseases|Hypotonia|_ataxia|_developmental_delay|_and_tooth_enamel_defect_syndrome": 1,
    "CTBP1-related_disorder": 3,
    "Hypotonia|_ataxia|_developmental_delay|_and_tooth_enamel_defect_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "CTBP1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Hypotonia|_ataxia|_developmental_delay|_and_tooth_enamel_defect_syndrome|not_provided": 1,
    "4p_partial_monosomy_syndrome|Hypotonia|_ataxia|_developmental_delay|_and_tooth_enamel_defect_syndrome|CTBP1-related_disorder|not_provided": 1,
    "UV-sensitive_syndrome_3": 4,
    "UVSSA-related_disorder": 13,
    "UVSSA-related_disorder|not_provided": 2,
    "UV-sensitive_syndrome_3|not_provided": 1,
    "FGFR3-related_disorder|not_provided": 34,
    "Achondroplasia": 8,
    "Hepatoblastoma|not_provided|not_specified": 1,
    "Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Muenke_syndrome|Colorectal_cancer|Achondroplasia|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Thanatophoric_dysplasia_type_1|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Malignant_tumor_of_urinary_bladder|Germ_cell_tumor_of_testis|Epidermal_nevus|Thanatophoric_dysplasia|_type_2|Lacrimoauriculodentodigital_syndrome_2|Hypochondroplasia": 1,
    "FGFR3-related_disorder|Achondroplasia|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus|Germ_cell_tumor_of_testis": 1,
    "not_provided|Muenke_syndrome": 1,
    "not_provided|FGFR3-related_disorder": 19,
    "Achondroplasia|Levy-Hollister_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Muenke_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Hypochondroplasia|Cervical_cancer|Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Malignant_tumor_of_testis|Crouzon_syndrome-acanthosis_nigricans_syndrome|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Carcinoma_of_colon|FGFR3-related_disorder|not_provided": 1,
    "Thanatophoric_dysplasia|_type_2": 1,
    "not_provided|Hypochondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Achondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Muenke_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2": 1,
    "Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|not_provided": 1,
    "Epidermal_nevus": 1,
    "Achondroplasia|Muenke_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Crouzon_syndrome-acanthosis_nigricans_syndrome|Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Colorectal_cancer|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Levy-Hollister_syndrome|Hypochondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Germ_cell_tumor_of_testis|not_specified|not_provided|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|not_specified|not_provided": 3,
    "Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|not_provided": 1,
    "FGFR3-related_disorder": 24,
    "FGFR3-related_disorder|not_provided|Achondroplasia": 1,
    "LADD_syndrome_1": 2,
    "not_provided|Hypochondroplasia|Inborn_genetic_diseases": 1,
    "Muenke_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|FGFR3-related_disorder": 1,
    "Craniosynostosis_syndrome|Genu_varum|Short_stature|Skeletal_dysplasia|Hypochondroplasia|Germ_cell_tumor_of_testis|Lacrimoauriculodentodigital_syndrome_2|Achondroplasia|Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Colorectal_cancer|Muenke_syndrome|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|not_provided": 1,
    "not_provided|not_specified|Achondroplasia": 1,
    "Inborn_genetic_diseases|not_provided|Muenke_syndrome": 1,
    "not_provided|Intellectual_disability|FGFR3-related_disorder": 1,
    "not_specified|FGFR3-related_disorder|not_provided": 1,
    "Crouzon_syndrome-acanthosis_nigricans_syndrome|not_provided": 1,
    "FGFR3-related_chondrodysplasia|Carcinoma_of_colon|Malignant_tumor_of_testis|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Achondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Epidermal_nevus|Thanatophoric_dysplasia_type_1|Cervical_cancer|Hypochondroplasia|Thanatophoric_dysplasia|_type_2|Levy-Hollister_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Lacrimoauriculodentodigital_syndrome_2|Germ_cell_tumor_of_testis|Colorectal_cancer|Connective_tissue_disorder|FGFR3-related_disorder|not_provided|Seborrheic_keratosis|Multiple_myeloma|Skeletal_dysplasia_with_acanthosis_nigricans|See_cases|Bowed_humerus|Small_for_gestational_age|Short_ribs|Narrow_chest|Disproportionate_short-limb_short_stature|Growth_delay|Skeletal_dysplasia|Lethal_short-limbed_short_stature|Short_stature|Bell-shaped_thorax|Lower_limb_undergrowth|Upper_limb_undergrowth|Femoral_bowing|Hamartoma": 1,
    "Carcinoma_of_colon|Malignant_tumor_of_testis|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Achondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Epidermal_nevus|Thanatophoric_dysplasia_type_1|Cervical_cancer|Hypochondroplasia|Thanatophoric_dysplasia|_type_2|Levy-Hollister_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Connective_tissue_disorder|FGFR3-related_disorder|not_provided|Seborrheic_keratosis|Squamous_cell_lung_carcinoma|See_cases": 1,
    "FGFR3-related_chondrodysplasia|FGFR3-related_disorder|Crouzon_syndrome|Coronal_craniosynostosis|Generalized_non-motor_(absence)_seizure|Unilateral_renal_agenesis|Facial_asymmetry|Infantile_axial_hypotonia|Seizure|not_specified|Lacrimoauriculodentodigital_syndrome_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Achondroplasia|Epidermal_nevus|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Germ_cell_tumor_of_testis|Colorectal_cancer|Hypochondroplasia|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Cervical_cancer|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Saethre-Chotzen_syndrome|Abnormality_of_the_nervous_system|not_provided|Craniosynostosis_syndrome|Inborn_genetic_diseases": 1,
    "Short_stature|Hypochondroplasia|not_provided": 1,
    "Achondroplasia|Hypochondroplasia|not_provided": 1,
    "Lacrimoauriculodentodigital_syndrome_2": 1,
    "not_provided|not_specified|FGFR3-related_disorder": 3,
    "not_provided|FGFR3-related_disorder|Inborn_genetic_diseases": 1,
    "Hypochondroplasia": 4,
    "Achondroplasia|not_provided": 2,
    "not_provided|FGFR3-related_CATSHL_syndrome": 1,
    "not_provided|Achondroplasia": 3,
    "Hypochondroplasia|not_provided": 2,
    "FGFR3-related_disorder|Connective_tissue_disorder|not_specified|not_provided": 1,
    "Achondroplasia|Hypochondroplasia|Skeletal_dysplasia|not_provided": 1,
    "Cervical_cancer|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Achondroplasia|Lacrimoauriculodentodigital_syndrome_2|Colorectal_cancer|Hypochondroplasia|Germ_cell_tumor_of_testis|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia|not_provided": 1,
    "Thanatophoric_dysplasia_type_1|not_specified|not_provided": 1,
    "FGFR3-related_disorder|not_provided|Thanatophoric_dysplasia_type_1|Achondroplasia|See_cases": 1,
    "FGFR3-related_disorder|Connective_tissue_disorder|Epidermal_nevus|Carcinoma_of_colon|Malignant_tumor_of_testis|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia|_type_2|Levy-Hollister_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Thanatophoric_dysplasia_type_1|Muenke_syndrome|Hypochondroplasia|Malignant_tumor_of_urinary_bladder|Crouzon_syndrome-acanthosis_nigricans_syndrome|Cervical_cancer|Achondroplasia|Lacrimoauriculodentodigital_syndrome_2|Germ_cell_tumor_of_testis|Colorectal_cancer|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Achondroplasia|LADD_syndrome_1|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Epidermal_nevus|Germ_cell_tumor_of_testis|Thanatophoric_dysplasia_type_1|Cervical_cancer|Colorectal_cancer|Hypochondroplasia|Thanatophoric_dysplasia|_type_2|Crouzon_syndrome-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|FGFR3-related_disorder|not_provided": 1,
    "Muenke_syndrome|Cervical_cancer|Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Hypochondroplasia|Germ_cell_tumor_of_testis|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Colorectal_cancer|Levy-Hollister_syndrome|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Connective_tissue_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Craniosynostosis_syndrome|not_provided|Crouzon_syndrome-acanthosis_nigricans_syndrome": 1,
    "Classic_Hodgkin_lymphoma|not_provided": 1,
    "FGFR3-related_disorder|Connective_tissue_disorder": 1,
    "not_provided|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome": 1,
    "Achondroplasia|Germ_cell_tumor_of_testis|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Achondroplasia|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus|Germ_cell_tumor_of_testis": 1,
    "Craniosynostosis|_nonspecific": 2,
    "not_specified|Inborn_genetic_diseases|Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Hypochondroplasia|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Levy-Hollister_syndrome|not_provided": 1,
    "not_specified|FGFR3-related_disorder": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Hypochondroplasia": 1,
    "Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome": 3,
    "Craniosynostosis|_nonspecific|not_provided": 1,
    "Thanatophoric_dysplasia_type_1": 2,
    "Lacrimoauriculodentodigital_syndrome_2|not_specified|not_provided|Levy-Hollister_syndrome": 1,
    "not_provided|Levy-Hollister_syndrome": 2,
    "not_provided|Achondroplasia|Germ_cell_tumor_of_testis|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus": 1,
    "not_provided|Hypochondroplasia|Muenke_syndrome": 1,
    "Craniosynostosis|_nonspecific|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|not_provided": 1,
    "not_provided|Hypochondroplasia": 3,
    "not_provided|Inborn_genetic_diseases|Achondroplasia|Hypochondroplasia|Neurodevelopmental_delay": 1,
    "FGFR3-related_chondrodysplasia|FGFR3-related_disorder|not_provided|Hypochondroplasia|Achondroplasia|Neurodevelopmental_delay": 1,
    "Carcinoma_of_colon|Malignant_tumor_of_testis|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Achondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Epidermal_nevus|Thanatophoric_dysplasia_type_1|Cervical_cancer|Hypochondroplasia|Thanatophoric_dysplasia|_type_2|Levy-Hollister_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Lacrimoauriculodentodigital_syndrome_2|Germ_cell_tumor_of_testis|Colorectal_cancer|Connective_tissue_disorder|FGFR3-related_disorder|Inborn_genetic_diseases|not_provided|Larsen_syndrome|Short_stature": 1,
    "FGFR3-related_disorder|not_specified|not_provided": 1,
    "Achondroplasia|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus|Germ_cell_tumor_of_testis|not_provided": 1,
    "Connective_tissue_disorder|Achondroplasia|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus|Germ_cell_tumor_of_testis|not_provided": 1,
    "not_provided|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome": 3,
    "not_specified|not_provided|Achondroplasia|Inborn_genetic_diseases|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|Lacrimoauriculodentodigital_syndrome_2": 1,
    "not_provided|Sarcoma": 1,
    "Sarcoma": 4,
    "Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Epidermal_nevus|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Colorectal_cancer|Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Malignant_tumor_of_urinary_bladder|Germ_cell_tumor_of_testis|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Muenke_syndrome|Hypochondroplasia|Sarcoma|not_provided": 1,
    "not_provided|Achondroplasia|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Colorectal_cancer|Hypochondroplasia|Epidermal_nevus|Germ_cell_tumor_of_testis": 2,
    "not_provided|Malignant_tumor_of_urinary_bladder|Hypochondroplasia": 1,
    "Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Achondroplasia|Lacrimoauriculodentodigital_syndrome_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Epidermal_nevus|Germ_cell_tumor_of_testis|Thanatophoric_dysplasia_type_1|Cervical_cancer|Colorectal_cancer|Hypochondroplasia|Thanatophoric_dysplasia|_type_2|Crouzon_syndrome-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Thanatophoric_dysplasia|FGFR3-related_disorder|not_provided|Multiple_myeloma|Spermatocytic_seminoma|See_cases": 1,
    "FGFR3-related_chondrodysplasia|Malignant_tumor_of_urinary_bladder|Malignant_tumor_of_testis|Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Epidermal_nevus|Levy-Hollister_syndrome|Hypochondroplasia|Carcinoma_of_colon|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Muenke_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|FGFR3-related_disorder|not_provided": 1,
    "Levy-Hollister_syndrome|Cervical_cancer|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Achondroplasia|Colorectal_cancer|Hypochondroplasia|Germ_cell_tumor_of_testis|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Crouzon_syndrome-acanthosis_nigricans_syndrome|not_provided": 2,
    "Epidermal_nevus|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia|_type_2|Levy-Hollister_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Thanatophoric_dysplasia_type_1|Muenke_syndrome|Germ_cell_tumor_of_testis|Colorectal_cancer|Hypochondroplasia|Malignant_tumor_of_urinary_bladder|Crouzon_syndrome-acanthosis_nigricans_syndrome|Cervical_cancer|Achondroplasia|not_provided": 1,
    "not_provided|Squamous_cell_lung_carcinoma|not_specified": 3,
    "Cervical_cancer": 1,
    "not_provided|Crouzon_syndrome-acanthosis_nigricans_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Levy-Hollister_syndrome|Epidermal_nevus|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Germ_cell_tumor_of_testis|Hypochondroplasia|Achondroplasia|Colorectal_cancer": 1,
    "not_provided|Crouzon_syndrome-acanthosis_nigricans_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Malignant_tumor_of_testis|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Carcinoma_of_colon|Levy-Hollister_syndrome|Epidermal_nevus|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Hypochondroplasia|Achondroplasia": 1,
    "not_provided|Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Malignant_tumor_of_urinary_bladder|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Hypochondroplasia|Germ_cell_tumor_of_testis|Cervical_cancer|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Muenke_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Epidermal_nevus|LADD_syndrome_1|Colorectal_cancer": 1,
    "Cervical_cancer|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Colorectal_cancer|Thanatophoric_dysplasia_type_1|Achondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Malignant_tumor_of_urinary_bladder|Muenke_syndrome|Thanatophoric_dysplasia|_type_2|Lacrimoauriculodentodigital_syndrome_2|Hypochondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Germ_cell_tumor_of_testis|Epidermal_nevus|not_provided": 1,
    "FGFR3-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Crouzon_syndrome-acanthosis_nigricans_syndrome|Muenke_syndrome|Malignant_tumor_of_urinary_bladder|Hypochondroplasia|Malignant_tumor_of_testis|Levy-Hollister_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Epidermal_nevus|Carcinoma_of_colon|Achondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|not_provided|FGFR3-related_disorder": 1,
    "Muenke_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Achondroplasia|Germ_cell_tumor_of_testis|Colorectal_cancer|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Muenke_syndrome|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Hypochondroplasia|Lacrimoauriculodentodigital_syndrome_2|Cervical_cancer|Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Crouzon_syndrome-acanthosis_nigricans_syndrome|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|FGFR3-related_disorder": 1,
    "Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Levy-Hollister_syndrome|Malignant_tumor_of_urinary_bladder|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Cervical_cancer|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Epidermal_nevus|Muenke_syndrome|Hypochondroplasia|Germ_cell_tumor_of_testis|Colorectal_cancer|not_provided|not_specified": 1,
    "Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia": 1,
    "not_provided|Thanatophoric_dysplasia_type_1|See_cases": 1,
    "not_provided|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|FGFR3-related_disorder|Connective_tissue_disorder": 1,
    "Cervical_cancer|Achondroplasia|Crouzon_syndrome-acanthosis_nigricans_syndrome|Germ_cell_tumor_of_testis|Malignant_tumor_of_urinary_bladder|Camptodactyly-tall_stature-scoliosis-hearing_loss_syndrome|Levy-Hollister_syndrome|Epidermal_nevus|Thanatophoric_dysplasia_type_1|Thanatophoric_dysplasia|_type_2|Hypochondroplasia|Severe_achondroplasia-developmental_delay-acanthosis_nigricans_syndrome|Muenke_syndrome|Colorectal_cancer|not_provided": 1,
    "not_provided|Thanatophoric_dysplasia_type_1": 1,
    "Thanatophoric_dysplasia_type_1|Achondroplasia|not_provided": 1,
    "Thanatophoric_dysplasia_type_1|FGFR3-related_disorder|See_cases": 1,
    "Global_developmental_delay|LETM1-associated_clinical_spectrum_with_predominant_nervous_system_involvement|Neurodegeneration|_childhood-onset|_with_multisystem_involvement_due_to_mitochondrial_dysfunction": 1,
    "Neurodegeneration|_childhood-onset|_with_multisystem_involvement_due_to_mitochondrial_dysfunction|LETM1-associated_clinical_spectrum_with_predominant_nervous_system_involvement": 3,
    "Neurodegeneration|_childhood-onset|_with_multisystem_involvement_due_to_mitochondrial_dysfunction": 2,
    "not_provided|LETM1-related_disorder": 1,
    "Neurodegeneration|_childhood-onset|_with_multisystem_involvement_due_to_mitochondrial_dysfunction|not_provided": 1,
    "not_provided|LETM1-associated_clinical_spectrum_with_predominant_nervous_system_involvement": 2,
    "LETM1-associated_clinical_spectrum_with_predominant_nervous_system_involvement": 3,
    "SRD5A3-congenital_disorder_of_glycosylation": 106,
    "LETM1-associated_clinical_spectrum_with_predominant_nervous_system_involvement|Neurodegeneration|_childhood-onset|_with_multisystem_involvement_due_to_mitochondrial_dysfunction": 1,
    "not_provided|4p_partial_monosomy_syndrome": 2,
    "4p_partial_monosomy_syndrome|not_provided": 2,
    "Wolf-Hirschhorn_like_syndrome": 2,
    "Rauch-Steindl_syndrome": 44,
    "NSD2-related_disorder": 16,
    "Rauch-Steindl_syndrome|not_provided": 5,
    "not_provided|NSD2-related_disorder": 13,
    "NSD2-related_disorder|not_provided": 6,
    "Inborn_genetic_diseases|Rauch-Steindl_syndrome": 2,
    "Wolf-Hirschhorn_like_syndrome|Inborn_genetic_diseases": 1,
    "NSD2-associated_disorder|atypical_Wolf-Hirschhorn_syndrome": 1,
    "4p_partial_monosomy_syndrome|Wolf-Hirschhorn_like_syndrome": 3,
    "not_provided|Rauch-Steindl_syndrome": 2,
    "Rauch-Steindl_syndrome|NSD2-related_disorder|not_provided|Global_developmental_delay|Neurodevelopmental_delay|4p_partial_monosomy_syndrome": 1,
    "NSD2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "WHSC1-related_disorder": 1,
    "NSD2-related_neurodevelopmental_disorder": 1,
    "Clubfoot|Macroglossia|Ventricular_septal_defect|Hypoglycemia|Enlarged_kidney|Furrowed_tongue|Hepatomegaly|Thrombocytopenia|Persistent_patent_ductus_venosus|Retrognathia|Intracranial_hemorrhage|Anemia|Hypertrophic_cardiomyopathy|Neurodevelopmental_delay|Rauch-Steindl_syndrome|Lymphoma": 1,
    "NSD2-related_disorder|Rauch-Steindl_syndrome": 1,
    "4p_partial_monosomy_syndrome|Rauch-Steindl_syndrome|not_provided|NSD2-related_disorder": 1,
    "Inborn_genetic_diseases|4p_partial_monosomy_syndrome|not_provided": 1,
    "not_provided|NELFA-related_disorder": 3,
    "NELFA-related_disorder|not_provided": 1,
    "NAT8L-related_disorder": 2,
    "N-acetylaspartate_deficiency": 1,
    "SH3BP2-related_disorder": 5,
    "Inborn_genetic_diseases|SH3BP2-related_disorder": 1,
    "Fibrous_dysplasia_of_jaw": 613,
    "not_provided|Fibrous_dysplasia_of_jaw": 29,
    "Fibrous_dysplasia_of_jaw|Inborn_genetic_diseases": 29,
    "Inborn_genetic_diseases|Fibrous_dysplasia_of_jaw": 33,
    "not_specified|Fibrous_dysplasia_of_jaw": 4,
    "not_provided|not_specified|Fibrous_dysplasia_of_jaw": 2,
    "SH3BP2-related_disorder|not_provided|Fibrous_dysplasia_of_jaw": 2,
    "Fibrous_dysplasia_of_jaw|Intellectual_disability|SH3BP2-related_disorder": 1,
    "SH3BP2-related_disorder|Fibrous_dysplasia_of_jaw|not_provided": 2,
    "not_specified|not_provided|Fibrous_dysplasia_of_jaw": 3,
    "Fibrous_dysplasia_of_jaw|not_provided|not_specified": 3,
    "not_provided|SH3BP2-related_disorder|Fibrous_dysplasia_of_jaw": 1,
    "not_provided|Inborn_genetic_diseases|Fibrous_dysplasia_of_jaw": 3,
    "SH3BP2-related_disorder|Fibrous_dysplasia_of_jaw": 6,
    "SH3BP2-related_disorder|Inborn_genetic_diseases|Fibrous_dysplasia_of_jaw": 1,
    "not_provided|Fibrous_dysplasia_of_jaw|not_specified": 1,
    "Fibrous_dysplasia_of_jaw|not_provided": 17,
    "Inborn_genetic_diseases|Fibrous_dysplasia_of_jaw|not_specified": 1,
    "not_provided|Fibrous_dysplasia_of_jaw|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fibrous_dysplasia_of_jaw|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|not_provided|Fibrous_dysplasia_of_jaw": 1,
    "Inborn_genetic_diseases|not_provided|Fibrous_dysplasia_of_jaw": 2,
    "Fibrous_dysplasia_of_jaw|not_specified": 1,
    "Fibrous_dysplasia_of_jaw|Congenital_heart_disease|SH3BP2-related_disorder": 1,
    "Fibrous_dysplasia_of_jaw|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Fibrous_dysplasia_of_jaw|Inborn_genetic_diseases": 1,
    "Fibrous_dysplasia_of_jaw|not_specified|SH3BP2-related_disorder": 1,
    "Fibrous_dysplasia_of_jaw|SH3BP2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Fibrous_dysplasia_of_jaw|SH3BP2-related_disorder": 1,
    "ADD1-related_disorder": 1,
    "hydrochlorothiazide_response_-_Efficacy|Hypertension|_salt-sensitive_essential|_susceptibility_to": 1,
    "not_specified|Huntington_disease": 1,
    "Huntington_disease|not_specified": 1,
    "Huntington_disease": 7,
    "Huntington_disease|Lopes-Maciel-Rodan_syndrome": 1,
    "HTT-related_disorder": 30,
    "Lopes-Maciel-Rodan_syndrome": 9,
    "not_provided|Lopes-Maciel-Rodan_syndrome|Huntington_disease": 2,
    "not_provided|HTT-related_disorder": 3,
    "Lopes-Maciel-Rodan_syndrome|not_provided": 1,
    "not_specified|Lopes-Maciel-Rodan_syndrome|not_provided": 1,
    "Lopes-Maciel-Rodan_syndrome|not_specified": 1,
    "Huntington_disease|Lopes-Maciel-Rodan_syndrome|not_provided": 2,
    "not_provided|Huntington_disease": 1,
    "Huntington_disease|not_provided": 1,
    "Lopes-Maciel-Rodan_syndrome|Huntington_disease": 1,
    "not_specified|DOK7-related_disorder|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 572,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 17,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 12,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 129,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 19,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Ritscher-Schinzel_syndrome_2|Fetal_akinesia_deformation_sequence_3|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided": 19,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|DOK7-related_disorder": 3,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 10,
    "not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|DOK7-related_disorder": 2,
    "not_specified|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 2,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|DOK7-related_disorder": 3,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided|not_specified": 3,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_specified": 9,
    "Congenital_myasthenic_syndrome_10": 12,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided": 16,
    "not_provided|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_specified|not_provided": 4,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_specified|not_provided": 11,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Inborn_genetic_diseases|not_provided": 7,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided|Inborn_genetic_diseases": 5,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Inborn_genetic_diseases": 7,
    "not_specified|DOK7-related_disorder|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "not_specified|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided": 5,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "DOK7-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 4,
    "not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_specified": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_specified|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided|Inborn_genetic_diseases": 4,
    "DOK7-related_disorder": 11,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 3,
    "Congenital_myasthenic_syndrome_10|not_provided": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|not_provided|Congenital_myasthenic_syndrome|DOK7-related_disorder|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided|not_specified": 3,
    "not_specified|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided|Fetal_akinesia_deformation_sequence_3": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_3": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|not_provided": 1,
    "Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3": 1,
    "Congenital_myasthenic_syndrome|not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3": 1,
    "not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 17,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_3": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|DOK7-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided|DOK7-related_disorder": 1,
    "not_provided|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1": 1,
    "Fetal_akinesia_deformation_sequence_3|not_specified|not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_3": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3": 1,
    "not_provided|Congenital_myasthenic_syndrome_10": 3,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided|Fetal_akinesia_deformation_sequence_3|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 3,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|See_cases": 1,
    "Fetal_akinesia_deformation_sequence_3|not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 2,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_3|not_provided": 3,
    "Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_10": 1,
    "not_specified|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 2,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided": 8,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|DOK7-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 2,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|DOK7-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided": 4,
    "not_specified|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided": 4,
    "DOK7-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Inborn_genetic_diseases": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_specified|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1": 3,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided|DOK7-related_disorder": 2,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided|not_specified": 1,
    "Fetal_akinesia_deformation_sequence_1": 7,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|DOK7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10": 1,
    "DOK7-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Inborn_genetic_diseases|not_provided": 1,
    "DOK7-related_disorder|not_specified|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 2,
    "not_provided|DOK7-related_disorder|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1": 1,
    "DOK7-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3": 3,
    "not_provided|not_specified|DOK7-related_disorder|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "DOK7-related_disorder|Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Ritscher-Schinzel_syndrome_2|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 1,
    "Ritscher-Schinzel_syndrome_2|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|DOK7-related_disorder": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|not_provided": 2,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10": 7,
    "DOK7-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome|not_provided|Rett_syndrome": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided|Fetal_akinesia_deformation_sequence_3": 1,
    "Fetal_akinesia_deformation_sequence_3|Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "DOK7-related_disorder|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided|Fetal_akinesia_deformation_sequence_3": 1,
    "Fetal_akinesia_deformation_sequence_3|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|Congenital_myasthenic_syndrome|not_provided|See_cases": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|not_provided": 2,
    "not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 1,
    "Fetal_akinesia_deformation_sequence_3|Congenital_myasthenic_syndrome_10|Inborn_genetic_diseases|not_provided|Fetal_akinesia_deformation_sequence_1": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_10|not_provided|not_specified|Fetal_akinesia_deformation_sequence_3": 1,
    "not_provided|Inborn_genetic_diseases|DOK7-related_disorder|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_3|not_provided": 1,
    "Abnormality_of_the_musculature|not_provided|Congenital_myasthenic_syndrome_10|Fetal_akinesia_deformation_sequence_1": 1,
    "not_provided|DOK7-related_disorder": 5,
    "DOK7-related_disorder|not_provided": 2,
    "LRPAP1-related_disorder": 4,
    "not_provided|LRPAP1-related_disorder": 6,
    "Myopia_23|_autosomal_recessive": 4,
    "LRPAP1-related_disorder|not_provided": 4,
    "not_specified|LRPAP1-related_disorder": 1,
    "Rare_isolated_myopia": 1,
    "ADRA2C-related_disorder": 6,
    "MSX1-related_disorder": 7,
    "Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|MSX1-related_disorder": 2,
    "Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 49,
    "Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|not_provided": 5,
    "not_provided|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 2,
    "MSX1-related_disorder|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 3,
    "Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|Tooth_agenesis|_selective|_1|Orofacial_cleft_5": 1,
    "Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|Orofacial_cleft_5": 1,
    "MSX1-related_selective_tooth_agenesis_with_or_without_orofacial_cleft": 1,
    "Inborn_genetic_diseases|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 1,
    "Orofacial_cleft_5": 2,
    "Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|Orofacial_cleft_5|not_provided": 1,
    "Tooth_agenesis|_selective|_1|Orofacial_cleft_5|MSX1-related_disorder|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 1,
    "MSX1-related_disorder|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|not_provided": 1,
    "Oligodontia": 11,
    "not_provided|Tooth_agenesis|_selective|_1|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 1,
    "Tooth_agenesis|_selective|_1|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 1,
    "Inborn_genetic_diseases|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome|not_provided": 1,
    "Craniosynostosis_syndrome|not_specified|Hypoplastic_enamel-onycholysis-hypohidrosis_syndrome": 1,
    "not_provided|Ellis-van_Creveld_syndrome": 32,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome": 1184,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 1389,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|Inborn_genetic_diseases": 22,
    "EVC2-related_disorder": 6,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 31,
    "Ellis-van_Creveld_syndrome|not_specified|Curry-Hall_syndrome": 3,
    "Curry-Hall_syndrome": 6,
    "Inborn_genetic_diseases|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 33,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_specified": 16,
    "Ellis-van_Creveld_syndrome|Inborn_genetic_diseases": 2,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided": 51,
    "not_provided|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome": 27,
    "not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ellis-van_Creveld_syndrome": 5,
    "not_specified|not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 10,
    "not_specified|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided": 5,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided|EVC2-related_disorder": 2,
    "Inborn_genetic_diseases|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided": 2,
    "EVC2-related_disorder|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome": 6,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided|not_specified": 8,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|EVC2-related_disorder": 5,
    "EVC2-related_disorder|Inborn_genetic_diseases|not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 1,
    "EVC2-related_disorder|not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 1,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|not_provided|not_specified": 5,
    "not_provided|EVC2-related_disorder": 1,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|Inborn_genetic_diseases": 30,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|not_provided": 31,
    "Inborn_genetic_diseases|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome": 37,
    "Ellis-van_Creveld_syndrome|EVC2-related_disorder|Curry-Hall_syndrome": 1,
    "EVC2-related_disorder|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 5,
    "not_provided|EVC2-related_disorder|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|Jeune_thoracic_dystrophy": 1,
    "not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_specified": 8,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|EVC2-related_disorder": 6,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|Jeune_thoracic_dystrophy": 1,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|not_specified": 7,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_specified|not_provided": 16,
    "Ellis-van_Creveld_syndrome|Inborn_genetic_diseases|not_provided|Curry-Hall_syndrome": 1,
    "Ellis-van_Creveld_syndrome|EVC2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome": 1,
    "Ellis-van_Creveld_syndrome|Inborn_genetic_diseases|Curry-Hall_syndrome": 8,
    "Ellis-van_Creveld_syndrome|not_provided": 16,
    "Ellis-van_Creveld_syndrome|not_specified|not_provided|Curry-Hall_syndrome": 2,
    "Type_IV_short_rib_polydactyly_syndrome|Ellis-van_Creveld_syndrome|EVC2-related_disorder|Curry-Hall_syndrome": 1,
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    "not_provided|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|not_specified": 3,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|Type_IV_short_rib_polydactyly_syndrome": 1,
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    "EVC-related_disorder|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome": 3,
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    "not_provided|Ellis-van_Creveld_syndrome|not_specified|Curry-Hall_syndrome|Inborn_genetic_diseases": 1,
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    "not_specified|EVC-related_disorder|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided": 1,
    "not_specified|Ellis-van_Creveld_syndrome": 2,
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    "Ellis-van_Creveld_syndrome|not_specified|Curry-Hall_syndrome|not_provided|EVC-related_disorder": 1,
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    "not_provided|EVC-related_disorder|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|not_specified": 1,
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    "not_specified|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|Inborn_genetic_diseases": 2,
    "Ellis-van_Creveld_syndrome|not_specified|Curry-Hall_syndrome|EVC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Ellis-van_Creveld_syndrome|EVC-related_disorder|Curry-Hall_syndrome": 1,
    "Ellis-van_Creveld_syndrome|not_specified": 1,
    "Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|EVC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Ellis-van_Creveld_syndrome|not_specified|Curry-Hall_syndrome|not_provided": 1,
    "not_provided|Curry-Hall_syndrome|Ellis-van_Creveld_syndrome|Inborn_genetic_diseases": 1,
    "Ellis-van_Creveld_syndrome|EVC-related_disorder|Curry-Hall_syndrome|not_provided": 1,
    "EVC-associated_disorder|Ellis-van_Creveld_syndrome|Curry-Hall_syndrome|not_provided": 1,
    "EVC-related_disorder|Ellis-van_Creveld_syndrome": 1,
    "CRMP1-related_neurodevelopmental_disorder": 1,
    "not_provided|Wolfram_syndrome_1": 51,
    "WFS1-related_disorder": 16,
    "Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6": 4,
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    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 6,
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    "Wolfram_syndrome_1": 65,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 17,
    "WFS1-Related_Spectrum_Disorders|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 3,
    "not_specified|Wolfram_syndrome_1": 17,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified": 1,
    "Wolfram_syndrome_1|not_specified": 5,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome": 3,
    "not_specified|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1": 68,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided": 43,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Monogenic_diabetes|not_provided": 1,
    "not_specified|not_provided|Wolfram_syndrome_1|Type_2_diabetes_mellitus|WFS1-Related_Spectrum_Disorders|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome": 1,
    "not_provided|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 15,
    "not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided": 9,
    "Wolfram_syndrome_1|not_provided": 60,
    "WFS1-Related_Spectrum_Disorders|Cataract_41|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1": 1,
    "not_specified|Wolfram_syndrome_1|not_provided": 10,
    "Wolfram_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|WFS1-Related_Spectrum_Disorders|not_specified|not_provided": 2,
    "Wolfram_syndrome_1|not_provided|WFS1-related_disorder|not_specified": 1,
    "WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 7,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Cataract_41": 10,
    "Inborn_genetic_diseases|Meniere_disease|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|WFS1-related_disorder|not_provided": 1,
    "not_provided|Wolfram_syndrome_1|not_specified": 6,
    "not_specified|not_provided|WFS1-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Wolfram_syndrome_1": 1,
    "Wolfram_syndrome_1|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 3,
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    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Monogenic_diabetes": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|WFS1-Related_Spectrum_Disorders|Type_2_diabetes_mellitus": 1,
    "not_provided|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1|WFS1-related_disorder": 2,
    "Monogenic_diabetes|not_specified|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Inborn_genetic_diseases|not_provided|Wolfram_syndrome_1": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|WFS1-Related_Spectrum_Disorders|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Optic_atrophy": 1,
    "Wolfram_syndrome_1|not_provided|not_specified": 6,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided|Inborn_genetic_diseases": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Cataract_41": 2,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_specified|not_provided": 3,
    "Monogenic_diabetes|Inborn_genetic_diseases|not_specified|not_provided|Wolfram_syndrome_1": 1,
    "Wolfram_syndrome_1|Type_2_diabetes_mellitus": 1,
    "WFS1-related_disorder|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_specified|not_provided": 2,
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    "Diabetes_mellitus|WFS1-related_disorder|not_specified|not_provided|Monogenic_diabetes": 1,
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    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified|not_provided": 1,
    "Wolfram_syndrome_1|Optic_atrophy|not_provided": 3,
    "Wolfram_syndrome_1|Cataract_41|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided": 1,
    "Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 6,
    "Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|Hereditary_ataxia|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome|Spastic_ataxia": 1,
    "WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified|Wolfram_syndrome_1": 1,
    "WFS1-Related_Spectrum_Disorders|Retinal_dystrophy|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41|Wolfram_syndrome|not_provided": 1,
    "WFS1-related_disorder|not_provided|Wolfram_syndrome_1": 1,
    "Wolfram-like_syndrome|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41|Inborn_genetic_diseases|not_provided": 1,
    "WFS1-related_disorder|not_provided": 12,
    "Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|WFS1-related_disorder|not_provided": 1,
    "Wolfram_syndrome_1|Optic_atrophy": 1,
    "not_provided|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1": 23,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided|WFS1-related_disorder": 3,
    "not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|not_specified": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome|not_specified|not_provided|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_provided|Wolfram_syndrome_1|Cataract_41|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_specified": 1,
    "not_specified|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41": 2,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Cataract_41|not_specified|not_provided": 1,
    "Wolfram_syndrome_1|not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided": 4,
    "not_specified|not_provided|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided|WFS1-related_disorder": 2,
    "not_specified|not_provided|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1": 1,
    "Wolfram_syndrome_1|WFS1-related_disorder|not_provided": 2,
    "WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|not_specified": 1,
    "Wolfram_syndrome_1|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|not_provided|See_cases": 1,
    "Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1": 2,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|not_specified|not_provided": 2,
    "Monogenic_diabetes|not_provided|Wolfram_syndrome_1": 1,
    "not_provided|not_specified|Wolfram_syndrome_1": 6,
    "Inborn_genetic_diseases|Wolfram_syndrome_1|not_provided": 2,
    "not_provided|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|WFS1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 2,
    "WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Wolfram_syndrome_1|Type_2_diabetes_mellitus|Optic_atrophy|not_provided|WFS1-related_disorder": 1,
    "not_provided|Wolfram_syndrome_1|WFS1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 3,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|not_specified|not_provided": 11,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1": 7,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Monogenic_diabetes|not_provided|not_specified": 1,
    "WFS1-related_disorder|not_specified|not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 1,
    "not_provided|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41": 7,
    "Monogenic_diabetes|Wolfram_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Optic_atrophy": 4,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Retinal_dystrophy|not_specified|not_provided": 2,
    "not_provided|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 21,
    "not_specified|WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 2,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_specified|not_provided": 4,
    "not_specified|not_provided|Wolfram_syndrome_1": 8,
    "Wolfram_syndrome|not_provided|not_specified|Type_2_diabetes_mellitus|Diabetes_mellitus|_noninsulin-dependent|_association_with|Wolfram_syndrome_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Wolfram-like_syndrome|Inborn_genetic_diseases|Cataract_41|Type_2_diabetes_mellitus|not_specified|not_provided": 1,
    "Wolfram-like_syndrome|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram_syndrome_1|not_provided|WFS1-related_disorder|Inborn_genetic_diseases": 1,
    "Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|Hereditary_ataxia|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome": 5,
    "not_specified|not_provided|Wolfram_syndrome_1|WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|not_specified|not_provided|Lymphedema": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|WFS1-related_disorder": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders": 1,
    "WFS1-related_disorder|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided": 1,
    "Diabetes_mellitus|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|WFS1-related_disorder|not_provided": 1,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Inborn_genetic_diseases|not_provided": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|WFS1-related_disorder|not_specified|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome|WFS1-related_disorder|not_provided": 1,
    "WFS1-related_disorder|Inborn_genetic_diseases": 1,
    "Wolfram_syndrome|not_provided": 1,
    "not_provided|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1": 4,
    "Inborn_genetic_diseases|not_specified|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|not_provided|not_specified|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided": 3,
    "Optic_atrophy|Congenital_bilateral_perisylvian_syndrome|not_provided": 1,
    "Wolfram_syndrome_1|not_specified|not_provided": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Cataract_41|WFS1-related_disorder": 1,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|WFS1-Related_Spectrum_Disorders|not_specified|not_provided": 2,
    "Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided": 6,
    "Inborn_genetic_diseases|Wolfram_syndrome_1|not_provided|Type_2_diabetes_mellitus|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome": 1,
    "not_provided|Diabetes_mellitus": 2,
    "not_specified|WFS1-related_disorder|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_provided": 1,
    "Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided|Optic_atrophy": 1,
    "Monogenic_diabetes|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1": 1,
    "WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|not_specified|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|WFS1-related_disorder": 1,
    "WFS1-Related_Spectrum_Disorders|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|not_specified|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|not_specified": 2,
    "Monogenic_diabetes|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|not_specified": 1,
    "Monogenic_diabetes|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Rare_genetic_deafness": 1,
    "not_specified|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "Optic_atrophy|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_provided": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_provided": 6,
    "WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided": 4,
    "Meniere_disease|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Monogenic_diabetes|not_provided|Retinal_dystrophy|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1": 1,
    "not_specified|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|Wolfram_syndrome_1": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_specified": 1,
    "not_provided|Wolfram-like_syndrome": 3,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|Wolfram_syndrome_1|Type_2_diabetes_mellitus|Cataract_41|Wolfram-like_syndrome": 1,
    "Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|WFS1-related_disorder|Monogenic_diabetes|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Wolfram-like_syndrome": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|Wolfram_syndrome_1|Type_2_diabetes_mellitus|Cataract_41|Wolfram-like_syndrome|WFS1-Related_Spectrum_Disorders": 1,
    "not_provided|Spastic_ataxia|WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41": 1,
    "Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1": 3,
    "Optic_atrophy|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_provided|See_cases": 1,
    "not_provided|Wolfram_syndrome_1|Cataract_41|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 2,
    "not_provided|WFS1-Related_Spectrum_Disorders|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_provided|Wolfram_syndrome": 1,
    "Wolfram_syndrome_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|WFS1-Related_Spectrum_Disorders": 1,
    "not_provided|Wolfram_syndrome_1|not_specified|WFS1-related_disorder|Inborn_genetic_diseases": 1,
    "WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Rare_genetic_deafness": 1,
    "Cataract_41": 2,
    "not_provided|Inborn_genetic_diseases|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1": 1,
    "WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Monogenic_diabetes|not_specified|not_provided": 1,
    "not_provided|Wolfram_syndrome_1|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|not_specified": 1,
    "not_specified|not_provided|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|Meniere_disease|not_specified|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_specified|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided": 1,
    "Inborn_genetic_diseases|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|not_specified|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified|not_provided|WFS1-Related_Spectrum_Disorders": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1": 3,
    "WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Hearing_impairment": 1,
    "Inborn_genetic_diseases|not_provided|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_provided|not_specified": 1,
    "WFS1-related_disorder|not_specified|Wolfram_syndrome_1|not_provided": 1,
    "not_provided|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Optic_atrophy": 1,
    "Wolfram_syndrome_1|Diabetes_mellitus|not_provided": 1,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|WFS1-related_disorder|not_provided": 1,
    "WFS1-related_disorder|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Spastic_ataxia|Hearing_impairment|Inborn_genetic_diseases|not_specified": 1,
    "Cataract_41|not_provided": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders": 1,
    "not_provided|WFS1-related_disorder": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6": 8,
    "Wolfram_syndrome_1|WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Inborn_genetic_diseases": 1,
    "Wolfram_syndrome_1|WFS1-related_disorder": 1,
    "Rare_genetic_deafness|Wolfram_syndrome_1": 1,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided|Optic_atrophy": 1,
    "Inborn_genetic_diseases|not_provided|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_specified": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram-like_syndrome|not_provided": 3,
    "not_specified|WFS1-related_disorder|not_provided|Wolfram_syndrome_1": 2,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|not_specified|not_provided|Optic_atrophy": 1,
    "WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 1,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided": 3,
    "Auditory_neuropathy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1": 1,
    "Wolfram-like_syndrome|Wolfram_syndrome_1|WFS1-related_disorder|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|not_provided": 1,
    "Diabetes_mellitus": 5,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41|Wolfram-like_syndrome|Type_2_diabetes_mellitus": 1,
    "not_provided|Wolfram-like_syndrome|Wolfram_syndrome_1": 2,
    "Wolfram_syndrome_1|not_provided|Optic_atrophy": 1,
    "Optic_neuropathy|not_provided": 2,
    "WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|WFS1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|WFS1-related_disorder|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Wolfram-like_syndrome|Optic_atrophy|Cataract_41|Type_2_diabetes_mellitus|not_specified|not_provided": 1,
    "Monogenic_diabetes|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Wolfram_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "WFS1-related_disorder|not_specified|not_provided|Wolfram_syndrome_1": 2,
    "Hereditary_ataxia|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|not_provided|WFS1-Related_Spectrum_Disorders": 1,
    "not_provided|Wolfram_syndrome_1|Inborn_genetic_diseases": 1,
    "Monogenic_hearing_loss|Optic_atrophy|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Diabetes_mellitus|not_specified|Wolfram_syndrome|Retinal_dystrophy|not_provided": 1,
    "Optic_atrophy|WFS1-related_disorder|Inborn_genetic_diseases|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome|not_provided": 1,
    "not_specified|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_provided": 1,
    "Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 2,
    "not_specified|Wolfram_syndrome_1|not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Inborn_genetic_diseases|Wolfram_syndrome": 1,
    "Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Wolfram_syndrome_1|WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41": 1,
    "not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41": 1,
    "not_specified|WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1": 1,
    "not_provided|Wolfram_syndrome_1|Type_2_diabetes_mellitus|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Inborn_genetic_diseases|WFS1-Related_Spectrum_Disorders": 1,
    "WFS1-Related_Spectrum_Disorders|not_provided|not_specified|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Type_2_diabetes_mellitus|Inborn_genetic_diseases|not_provided|Wolfram-like_syndrome|WFS1-related_disorder": 1,
    "WFS1-related_disorder|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|not_specified|Type_2_diabetes_mellitus|Wolfram_syndrome_1|not_provided|Inborn_genetic_diseases|Optic_atrophy|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Inborn_genetic_diseases|WFS1-related_disorder|not_provided|not_specified|Wolfram_syndrome_1": 1,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome|WFS1-related_disorder": 1,
    "Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Monogenic_diabetes|not_specified|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Optic_atrophy": 1,
    "WFS1-related_disorder|not_provided|Wolfram_syndrome_1|not_specified": 1,
    "not_provided|Diabetes_mellitus|WFS1-Related_Spectrum_Disorders|Cataract_41|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided": 3,
    "Monogenic_diabetes|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|WFS1-related_disorder|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 1,
    "WFS1-related_disorder|Wolfram_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Rare_genetic_deafness|Monogenic_diabetes|not_provided": 1,
    "Wolfram_syndrome_1|Monogenic_diabetes|not_provided": 1,
    "Wolfram-like_syndrome|Wolfram_syndrome_1|not_specified|not_provided": 1,
    "WFS1-related_disorder|Wolfram_syndrome_1|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|not_provided": 2,
    "not_provided|Diabetes": 1,
    "Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_specified|not_provided": 1,
    "Cataract_41|not_provided|Wolfram_syndrome_1": 1,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Spastic_ataxia|not_specified|not_provided": 1,
    "Wolfram_syndrome_1|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|WFS1-Related_Spectrum_Disorders|not_provided": 1,
    "Wolfram-like_syndrome|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|See_cases|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders": 1,
    "not_provided|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|not_specified|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|not_provided": 1,
    "Wolfram_syndrome_1|Wolfram-like_syndrome|WFS1-Related_Spectrum_Disorders|Diabetes_mellitus|not_specified|WFS1-related_disorder|Inborn_genetic_diseases|Optic_atrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Retinal_dystrophy|Hearing_impairment": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_specified|not_provided|WFS1-Related_Spectrum_Disorders|Cataract_41|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome": 1,
    "WFS1-related_disorder|not_specified|not_provided": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|WFS1-related_disorder|Childhood_onset_hearing_loss|Retinal_dystrophy|not_specified|not_provided": 1,
    "Monogenic_hearing_loss|not_provided": 3,
    "not_specified|Wolfram_syndrome_1|not_provided|WFS1-related_disorder|Wolfram-like_syndrome|Monogenic_diabetes": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|not_specified|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1": 1,
    "WFS1-spectrum_disorder|WFS1-related_disorder|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|not_provided|Rare_genetic_deafness|Optic_atrophy|Autosomal_dominant_nonsyndromic_hearing_loss|Inborn_genetic_diseases": 1,
    "Meniere_disease|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_provided|WFS1-related_disorder|Monogenic_diabetes|Optic_atrophy": 1,
    "Wolfram-like_syndrome|Wolfram_syndrome_1|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided|Hearing_impairment": 1,
    "Diabetes_mellitus|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-related_disorder|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1": 1,
    "Wolfram-like_syndrome|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41|not_provided": 1,
    "not_provided|Wolfram_syndrome_1|WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided": 1,
    "not_provided|Type_2_diabetes_mellitus|Wolfram_syndrome_1|WFS1-related_disorder": 1,
    "Monogenic_diabetes|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|not_provided|Retinal_dystrophy|WFS1-related_disorder|Inborn_genetic_diseases": 1,
    "WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Type_2_diabetes_mellitus": 2,
    "Wolfram_syndrome_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders": 1,
    "Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Cataract_41|Wolfram_syndrome_1|Type_2_diabetes_mellitus|Wolfram-like_syndrome": 2,
    "Monogenic_hearing_loss|Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "WFS1-Related_Spectrum_Disorders|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 3,
    "WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|Diabetes_mellitus|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|not_specified|not_provided": 1,
    "WFS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Wolfram_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram-like_syndrome|not_provided": 1,
    "Monogenic_diabetes|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided": 1,
    "WFS1-related_disorder|Type_2_diabetes_mellitus|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided": 1,
    "Wolfram_syndrome_1|WFS1-related_disorder|not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "WFS1-related_disorder|not_provided|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Cataract_41|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1": 1,
    "not_specified|Monogenic_diabetes|WFS1-related_disorder|not_provided|Inborn_genetic_diseases|Wolfram_syndrome_1": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_specified|not_provided": 2,
    "not_provided|not_specified|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 1,
    "WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1": 1,
    "Inborn_genetic_diseases|Cataract_41|Wolfram-like_syndrome|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided": 1,
    "Optic_atrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome|Cataract_41": 1,
    "not_provided|not_specified|Wolfram_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Wolfram-like_syndrome|Wolfram_syndrome|Wolfram_syndrome_1": 1,
    "Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_specified|not_provided": 1,
    "Wolfram_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "not_specified|Wolfram_syndrome_1|not_provided|WFS1-related_disorder": 1,
    "Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Optic_atrophy": 1,
    "WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Monogenic_diabetes|Inborn_genetic_diseases|WFS1-Related_Spectrum_Disorders|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus": 1,
    "Wolfram_syndrome": 1,
    "Wolfram_syndrome_1|Type_2_diabetes_mellitus|Monogenic_diabetes|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|not_specified|not_provided": 1,
    "not_provided|WFS1-related_disorder|not_specified": 1,
    "Optic_atrophy|Wolfram_syndrome_1|WFS1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss|Rare_genetic_deafness|not_provided": 1,
    "not_provided|not_specified|Wolfram_syndrome_1|WFS1-related_disorder": 1,
    "Wolfram_syndrome_1|Wolfram-like_syndrome": 1,
    "WFS1-Related_Spectrum_Disorders|WFS1-related_disorder|not_specified|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Inborn_genetic_diseases|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Diabetes_mellitus|Sensorineural_hearing_loss_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_provided|Hearing_impairment": 1,
    "Wolfram_syndrome_1|Inborn_genetic_diseases": 1,
    "WFS1-Related_Spectrum_Disorders|Monogenic_diabetes|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 1,
    "not_provided|WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1": 2,
    "not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Inborn_genetic_diseases|Cataract_41|Wolfram_syndrome_1|Type_2_diabetes_mellitus|Wolfram-like_syndrome": 2,
    "Wolfram_syndrome_1|not_provided|WFS1-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6": 1,
    "Type_2_diabetes_mellitus|Wolfram_syndrome_1": 1,
    "Inborn_genetic_diseases|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41|not_provided": 1,
    "Rare_genetic_deafness|Wolfram-like_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|WFS1-related_disorder|WFS1-Related_Spectrum_Disorders|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|Wolfram-like_syndrome|Wolfram_syndrome": 1,
    "Inborn_genetic_diseases|Spastic_ataxia|not_provided|not_specified": 1,
    "not_provided|Wolfram_syndrome_1|Autistic_behavior": 1,
    "Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Wolfram_syndrome_1|not_provided": 1,
    "Wolfram_syndrome_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Wolfram_syndrome_1|WFS1-related_disorder|Monogenic_diabetes|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_specified|not_provided": 2,
    "WFS1-related_disorder|Optic_atrophy|Wolfram-like_syndrome|Type_2_diabetes_mellitus|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|Cataract_41|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss|Retinal_dystrophy|Nonsyndromic_genetic_hearing_loss|not_provided|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|See_cases": 1,
    "WFS1-related_disorder|Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_specified|Wolfram-like_syndrome|Wolfram_syndrome_1|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|not_provided|Autistic_behavior": 1,
    "Wolfram-like_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Optic_atrophy": 1,
    "Monogenic_diabetes|WFS1-Related_Spectrum_Disorders|Cataract_41|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|Type_2_diabetes_mellitus|Wolfram-like_syndrome|Cataract_41|Wolfram_syndrome_1": 1,
    "WFS1-related_disorder|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram-like_syndrome|Cataract_41|Type_2_diabetes_mellitus|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram_syndrome_1|Wolfram-like_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|Type_2_diabetes_mellitus|Cataract_41|Wolfram-like_syndrome|not_provided|Wolfram_syndrome": 1,
    "Inborn_genetic_diseases|Wolfram_syndrome_1": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_provided|Wolfram_syndrome_1": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders": 4,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders|not_provided": 1,
    "WFS1-Related_Spectrum_Disorders|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided|Wolfram_syndrome_1": 2,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Nonsyndromic_Hearing_Loss|_Dominant": 3,
    "WFS1-Related_Spectrum_Disorders|Nonsyndromic_Hearing_Loss|_Dominant|Wolfram_syndrome_1": 1,
    "Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|WFS1-Related_Spectrum_Disorders": 1,
    "WFS1-Related_Spectrum_Disorders|Wolfram_syndrome_1|Autosomal_dominant_nonsyndromic_hearing_loss_6|not_provided": 2,
    "WFS1-Related_Spectrum_Disorders|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "Wolfram_syndrome_1|WFS1-Related_Spectrum_Disorders|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "MAN2B2-related_disorder": 2,
    "Congenital_disorder_of_glycosylation_type_1EE_with_or_without_immunodeficiency": 2,
    "not_provided|MAN2B2-related_disorder": 2,
    "not_specified|MAN2B2-related_disorder": 1,
    "not_specified|Congenital_disorder_of_glycosylation_type_1EE_with_or_without_immunodeficiency": 1,
    "BLOC1S4-related_condition": 1,
    "KIAA0232-related_disorder": 7,
    "KIAA0232-related_disorder|not_provided": 1,
    "Orofaciodigital_syndrome": 3,
    "CPZ-related_disorder": 36,
    "not_provided|CPZ-related_disorder": 6,
    "not_specified|CPZ-related_disorder": 1,
    "CPZ-related_disorder|not_provided": 1,
    "HMX1-related_disorder": 2,
    "not_provided|HMX1-related_disorder": 4,
    "not_provided|Oculoauricular_syndrome": 1,
    "HMX1-related_disorder|not_provided": 2,
    "Oculoauricular_syndrome": 3,
    "DRD5-related_disorder": 6,
    "not_provided|DRD5-related_disorder|not_specified": 1,
    "Oculocutaneous_albinism_type_1A": 31,
    "Schizophrenia|Hereditary_attention_deficit-hyperactivity_disorder": 1,
    "Attention_deficit-hyperactivity_disorder|_susceptibility_to|_7": 3,
    "not_provided|Hereditary_attention_deficit-hyperactivity_disorder": 3,
    "Hypouricemia|_renal|_2": 41,
    "not_provided|Hypouricemia|_renal|_2": 33,
    "Hypouricemia|_renal|_2|not_provided": 14,
    "Hypouricemia|_renal|_2|Inborn_genetic_diseases|not_provided": 1,
    "SLC2A9-related_disorder|not_provided": 2,
    "SLC2A9-related_disorder|not_provided|Hypouricemia|_renal|_2": 3,
    "Hypouricemia|_renal|_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|SLC2A9-related_disorder": 1,
    "SLC2A9-related_disorder": 5,
    "not_provided|SLC2A9-related_disorder|Hypouricemia|_renal|_2": 2,
    "Inborn_genetic_diseases|not_provided|Hypouricemia|_renal|_2": 1,
    "Uric_acid_concentration|_serum|_quantitative_trait_locus_2": 3,
    "Hypouricemia|_renal|_2|SLC2A9-related_disorder|not_provided|not_specified": 1,
    "not_provided|Dalmatian_hypouricemia": 26,
    "SLC2A9-related_disorder|Hypouricemia|_renal|_2": 1,
    "Hypouricemia|_renal|_2|not_provided|SLC2A9-related_disorder": 1,
    "not_provided|SLC2A9-related_disorder": 1,
    "Intellectual_developmental_disorder_61": 81,
    "Lazy_leukocyte_syndrome": 9,
    "WDR1-related_disorder|not_provided": 10,
    "WDR1-related_disorder": 3,
    "not_provided|WDR1-related_disorder": 11,
    "not_provided|WDR1_deficiency|WDR1-related_disorder": 1,
    "Inborn_genetic_diseases|Lazy_leukocyte_syndrome|not_provided": 1,
    "Lazy_leukocyte_syndrome|not_provided|WDR1-related_disorder": 1,
    "Lazy_leukocyte_syndrome|not_provided": 1,
    "not_provided|Lazy_leukocyte_syndrome": 1,
    "CLNK-related_disorder": 2,
    "Arteriosclerosis_disorder|Coronary_artery_disorder": 1,
    "not_provided|Cone-rod_dystrophy_18": 2,
    "RAB28-related_disorder": 2,
    "Retinal_dystrophy|Cone-rod_dystrophy_18": 1,
    "Cone-rod_dystrophy_18|Cone-rod_dystrophy": 1,
    "Cone-rod_dystrophy_18": 3,
    "Cone-rod_dystrophy_18|not_provided": 3,
    "Optic_atrophy|not_specified|not_provided": 3,
    "NKX3-2-related_disorder": 1,
    "not_provided|NKX3-2-related_disorder": 3,
    "NKX3-2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Spondylo-megaepiphyseal-metaphyseal_dysplasia": 4,
    "not_provided|Connective_tissue_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Spondylo-megaepiphyseal-metaphyseal_dysplasia|not_specified|not_provided": 1,
    "Connective_tissue_disorder|not_provided|NKX3-2-related_disorder": 1,
    "Connective_tissue_disorder|NKX3-2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Connective_tissue_disorder|NKX3-2-related_disorder": 1,
    "not_provided|Spondylo-megaepiphyseal-metaphyseal_dysplasia": 1,
    "not_provided|NKX3-2-related_disorder|Inborn_genetic_diseases": 1,
    "CC2D2A-related_disorder|Meckel_syndrome|_type_6|Joubert_syndrome_9": 3,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9": 10,
    "not_specified|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Joubert_syndrome_9": 1,
    "not_provided|CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9": 4,
    "Joubert_syndrome|Meckel-Gruber_syndrome": 3058,
    "Meckel-Gruber_syndrome|Joubert_syndrome": 1109,
    "COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93": 16,
    "not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Inborn_genetic_diseases": 2,
    "Joubert_syndrome_and_related_disorders|Retinitis_pigmentosa_93|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 50,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 31,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93": 7,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Optic_atrophy": 1,
    "CC2D2A-related_disorder": 29,
    "not_specified|Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93": 2,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 42,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_1": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9": 1,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 56,
    "not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 6,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 8,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Ciliopathy|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Retinitis_pigmentosa_93|Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "CC2D2A-related_disorder|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 4,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_specified|not_provided": 2,
    "not_provided|CC2D2A-related_disorder": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 4,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9": 75,
    "not_provided|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome": 4,
    "Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|not_provided": 2,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 34,
    "not_specified|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 20,
    "not_specified|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Meckel_syndrome|_type_6|CC2D2A-related_disorder|not_provided|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 52,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|Joubert_syndrome_9|not_provided|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder": 15,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 2,
    "Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome": 4,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6": 1,
    "COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Joubert_syndrome_9": 2,
    "Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "not_provided|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders|Retinal_dystrophy": 1,
    "not_specified|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 5,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 2,
    "Retinal_dystrophy|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 32,
    "CC2D2A-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|not_provided": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9": 3,
    "Joubert_syndrome|not_specified|Meckel-Gruber_syndrome|COACH_syndrome_1|Meckel_syndrome|_type_6|not_provided|Joubert_syndrome_1": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_1": 1,
    "not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|CC2D2A-related_disorder|Meckel_syndrome|_type_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 19,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_6": 15,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|not_provided|CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_specified|Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|CC2D2A-related_disorder": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Retinitis_pigmentosa_93|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|CC2D2A-related_disorder": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 29,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|CC2D2A-related_disorder|not_specified": 1,
    "Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9|not_provided|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "CC2D2A-related_disorder|Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_9|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 2,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Retinitis_pigmentosa_93|COACH_syndrome_2": 1,
    "CC2D2A-related_disorder|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "not_provided|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|Inborn_genetic_diseases": 1,
    "CC2D2A-related_disorder|Retinal_dystrophy|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome": 6,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 4,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Microcephaly|Polycystic_kidney_disease|Narrow_chest|Encephalocele|Polydactyly|_postaxial|_type_A1|Clubfoot|Oligohydramnios|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Congenital_heart_disease|CC2D2A-related_disorder|not_specified": 1,
    "Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Meckel-Gruber_syndrome|Joubert_syndrome": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|not_provided": 2,
    "Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Ciliopathy|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_9": 1,
    "COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome": 4,
    "Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Abnormality_of_prenatal_development_or_birth": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6": 3,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 8,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|not_provided|not_specified|Retinitis_pigmentosa_93|COACH_syndrome_2|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Anencephaly|Polydactyly|Renal_cyst": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9": 6,
    "Inborn_genetic_diseases|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome|CC2D2A-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_6|COACH_syndrome_1|Joubert_syndrome_9|COACH_syndrome_2|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_6": 1,
    "not_specified|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder|not_provided": 3,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|Inborn_genetic_diseases|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Retinitis_pigmentosa_93|COACH_syndrome_2": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|CC2D2A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9|Polycystic_kidney_disease|Encephalocele": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9": 2,
    "Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome_9|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder": 4,
    "Meckel_syndrome|_type_6|not_provided|not_specified|Joubert_syndrome_9": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|CC2D2A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|Inborn_genetic_diseases|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|COACH_syndrome_1": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9": 2,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|not_provided|Meckel_syndrome|_type_6": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|not_provided": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 9,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9": 1,
    "CC2D2A-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|COACH_syndrome_1|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "CC2D2A-related_disorder|Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|CC2D2A-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|not_provided": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 6,
    "not_specified|not_provided|Joubert_syndrome_1|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93": 2,
    "not_provided|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome": 4,
    "not_provided|Meckel_syndrome|_type_6|not_specified|Joubert_syndrome_9": 2,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided": 1,
    "CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_6": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_1|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|COACH_syndrome_1|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|Retinal_dystrophy|Optic_atrophy": 1,
    "Joubert_syndrome|CC2D2A-related_disorder|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6": 7,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Retinal_dystrophy|Joubert_syndrome_9|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2": 1,
    "Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9": 3,
    "CC2D2A-related_disorder|not_provided|not_specified|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CC2D2A-related_disorder|Inborn_genetic_diseases|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_6|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "CC2D2A-related_disorder|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "COACH_syndrome_1|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder|Joubert_syndrome_9": 1,
    "Joubert_syndrome_9|COACH_syndrome_1|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|CC2D2A-related_disorder": 1,
    "Retinal_dystrophy|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|CC2D2A-related_disorder|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder|not_provided|Meckel_syndrome|_type_6": 1,
    "Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|CC2D2A-related_disorder|Joubert_syndrome|COACH_syndrome_1": 1,
    "not_provided|CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified": 1,
    "Meckel_syndrome|_type_6|not_specified|Joubert_syndrome_9|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "CC2D2A-related_disorder|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "not_specified|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9|COACH_syndrome_1|Meckel_syndrome|_type_6|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1": 1,
    "CC2D2A-related_disorder|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|CC2D2A-related_disorder|COACH_syndrome_1|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9|not_specified": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|CC2D2A-related_disorder|Retinal_dystrophy|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Retinal_dystrophy|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_1": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_1": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 3,
    "Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided|Joubert_syndrome_9/15|_digenic|See_cases": 1,
    "Joubert_syndrome_9|COACH_syndrome_1": 1,
    "Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_9|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|not_provided": 1,
    "Meckel_syndrome|_type_6|COACH_syndrome_1|Joubert_syndrome_9": 1,
    "CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_9|Ciliopathy|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder|Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2": 1,
    "COACH_syndrome_2|Joubert_syndrome_9|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|See_cases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Polycystic_kidney_disease|Encephalocele": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|Inborn_genetic_diseases|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Neurodevelopmental_disorder|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Polydactyly|Meckel_syndrome|_type_6|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "COACH_syndrome_1|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "not_specified|Joubert_syndrome_9": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Inborn_genetic_diseases|Neonatal_encephalopathy": 1,
    "Ciliopathy|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome|CC2D2A-related_disorder": 1,
    "CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9|COACH_syndrome_1|Meckel_syndrome|_type_6|not_provided|Intellectual_disability": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|not_provided": 2,
    "Joubert_syndrome_9|not_provided": 1,
    "Meckel-Gruber_syndrome": 10,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|not_provided": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_1": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Inborn_genetic_diseases|not_provided|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|CC2D2A-related_disorder|Ciliopathy|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1": 1,
    "Joubert_syndrome_9|Retinal_dystrophy": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "COACH_syndrome_1|Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|CC2D2A-related_disorder|not_specified": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_9": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "not_provided|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_specified": 1,
    "not_provided|Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_1|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9|Retinitis_pigmentosa_93|COACH_syndrome_2|Meckel_syndrome|_type_6|Microcephaly|Clubfoot|Narrow_chest|Encephalocele|Oligohydramnios|Polycystic_kidney_disease|Polydactyly|_postaxial|_type_A1|Inborn_genetic_diseases|not_provided|Polydactyly|Renal_cyst|Anencephaly": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|COACH_syndrome_2|Meckel_syndrome|_type_6|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Microcephaly|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome_9|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_9|Meckel_syndrome|_type_6|CC2D2A-related_disorder|not_specified|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1": 2,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "Joubert_syndrome_9|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|CC2D2A-related_disorder|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|CC2D2A-related_disorder|Joubert_syndrome_9/15|_digenic|not_provided": 1,
    "Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Inborn_genetic_diseases": 1,
    "COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_provided|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_9": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Meckel_syndrome|_type_6|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_6|Joubert_syndrome_9|not_specified": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "COACH_syndrome_1": 8,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|CC2D2A-related_disorder": 1,
    "not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6|CC2D2A-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|CC2D2A-related_disorder|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Neurodevelopmental_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified": 7,
    "Joubert_syndrome_9|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_10|Meckel_syndrome|_type_6": 1,
    "Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|not_provided": 1,
    "Meckel_syndrome|_type_6|CC2D2A-related_disorder|COACH_syndrome_2|Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|COACH_syndrome_2|Retinitis_pigmentosa_93|not_specified|CC2D2A-related_disorder|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_2|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|Joubert_syndrome_9": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Joubert_syndrome_9|CC2D2A-related_disorder|Joubert_syndrome_and_related_disorders|Neurodevelopmental_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Ciliopathy|not_provided|Joubert_syndrome|COACH_syndrome_1|Meckel-Gruber_syndrome": 1,
    "not_provided|CC2D2A-related_disorder|not_specified|Meckel_syndrome|_type_6|COACH_syndrome_2|Retinitis_pigmentosa_93|Joubert_syndrome_9|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_9|Meckel_syndrome|_type_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|CC2D2A-related_disorder": 1,
    "CC2D2A-related_disorder|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "CC2D2A-related_disorder|Joubert_syndrome_9|Retinitis_pigmentosa_93|Meckel_syndrome|_type_6|COACH_syndrome_2|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_93": 1,
    "Meckel_syndrome|_type_6|Joubert_syndrome_9|CC2D2A-related_disorder|Optic_atrophy|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "CC2D2A-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders|not_provided|Joubert_syndrome_9": 1,
    "not_provided|Meckel_syndrome|_type_6|Retinitis_pigmentosa_93|COACH_syndrome_2|Joubert_syndrome_9|COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "CC2D2A-related_disorder|not_specified|not_provided|Joubert_syndrome_9|Meckel_syndrome|_type_6": 1,
    "not_specified|Joubert_syndrome_9|Meckel_syndrome|_type_6|not_provided": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 85,
    "Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 2,
    "Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinitis_pigmentosa": 6,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 10,
    "Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa|Stargardt_disease_4|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2": 4,
    "Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa|Stargardt_disease_4": 3,
    "Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa|not_provided": 2,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2": 1,
    "Stargardt_Disease|_Dominant|Macular_dystrophy|_retinal|Cone-Rod_Dystrophy|_Dominant|Retinitis_Pigmentosa|_Recessive": 3,
    "not_provided|Retinitis_pigmentosa_41|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 2,
    "not_provided|Inborn_genetic_diseases|Cone-rod_dystrophy_12|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_12|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Cone-rod_dystrophy_12": 11,
    "not_provided|Retinal_macular_dystrophy_type_2|Retinal_dystrophy": 1,
    "not_provided|PROM1-related_disorder": 7,
    "not_provided|Retinal_dystrophy|Stargardt_disease_4|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_12|Retinal_dystrophy": 1,
    "PROM1-related_disorder|not_provided": 8,
    "not_provided|Retinitis_pigmentosa_41|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinitis_pigmentosa_41|Retinal_macular_dystrophy_type_2": 1,
    "Cone-rod_dystrophy_12|Stargardt_disease_4|Retinitis_pigmentosa_41|Retinal_macular_dystrophy_type_2": 1,
    "Stargardt_disease_4|Retinal_dystrophy": 1,
    "not_provided|Stargardt_Disease|_Dominant|Macular_dystrophy|_retinal|Cone-Rod_Dystrophy|_Dominant|Retinitis_Pigmentosa|_Recessive|not_specified": 1,
    "Macular_dystrophy|_retinal|Stargardt_Disease|_Dominant|Cone-Rod_Dystrophy|_Dominant|Retinitis_Pigmentosa|_Recessive|not_provided|Retinal_dystrophy": 1,
    "Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinitis_pigmentosa_41|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Stargardt_disease_4|Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2": 1,
    "Retinal_macular_dystrophy_type_2": 2,
    "not_provided|Cone-rod_dystrophy_12|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 7,
    "Retinal_dystrophy|not_provided|Stargardt_disease_4|Retinitis_pigmentosa_41|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_12": 1,
    "not_provided|Cone-rod_dystrophy_12|PROM1-related_disorder|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|not_provided": 1,
    "Retinitis_pigmentosa_41|Retinal_macular_dystrophy_type_2|not_provided": 2,
    "not_provided|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_12|Retinitis_pigmentosa_41|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Cone-rod_dystrophy|Cone-rod_dystrophy_12": 1,
    "not_provided|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "not_provided|Retinal_macular_dystrophy_type_2": 1,
    "Retinitis_pigmentosa_41": 5,
    "Retinitis_pigmentosa|Stargardt_disease|not_provided|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Stargardt_disease_4|PROM1-related_disorder|Retinitis_pigmentosa|Optic_atrophy|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_2|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12": 1,
    "not_provided|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa": 3,
    "Stargardt_disease|Cone-rod_dystrophy_12|Retinitis_pigmentosa_41|not_provided": 1,
    "PROM1-related_disorder|Retinitis_pigmentosa_41|Leber_congenital_amaurosis|not_provided|Stargardt_disease|Cone-rod_dystrophy": 1,
    "Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Cone-rod_dystrophy_12": 1,
    "not_provided|Cone-rod_dystrophy_12|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|not_specified": 1,
    "not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Retinal_disorders|not_specified|not_provided|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "not_provided|Retinitis_pigmentosa_41": 3,
    "Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Cone-rod_dystrophy_12": 6,
    "Cone-rod_dystrophy|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12|Retinal_dystrophy|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|not_provided": 1,
    "PROM1-related_disorder|not_provided|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Retinitis_pigmentosa_41|Leber_congenital_amaurosis_1": 1,
    "not_provided|Retinitis_pigmentosa_41|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "PROM1-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|PROM1-related_disorder|Cone-rod_dystrophy_12": 1,
    "Cone-rod_dystrophy_12|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|not_provided|Retinal_dystrophy": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_41|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_12|Retinitis_pigmentosa|not_provided|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Retinal_dystrophy|not_provided|Retinal_macular_dystrophy_type_2": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa_41|Stargardt_disease_4|not_provided": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_12|not_provided|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Cone-rod_dystrophy|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|not_provided|Retinal_dystrophy": 1,
    "PROM1-related_disorder|Retinal_dystrophy|not_provided|Cone-rod_dystrophy_12": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|not_provided|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "not_provided|Stargardt_disease_4|Cone-rod_dystrophy_12|Retinitis_pigmentosa_41|Retinal_macular_dystrophy_type_2": 1,
    "not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinal_dystrophy": 3,
    "not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 2,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Stargardt_disease|Cone-rod_dystrophy_2|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12|Retinal_dystrophy|Retinitis_pigmentosa|PROM1-related_disorder": 1,
    "Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa_41|PROM1-related_disorder|not_provided|Retinitis_pigmentosa|Stargardt_disease_4": 1,
    "PROM1-related_disorder|not_provided|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12": 1,
    "Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|not_provided": 1,
    "Cone-rod_dystrophy_12|not_provided|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "PROM1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "Retinitis_pigmentosa_41|not_provided|Retinal_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy|Stargardt_disease_4|Cone-rod_dystrophy_12": 1,
    "Inborn_genetic_diseases|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Retinitis_pigmentosa|not_provided": 1,
    "Cone-rod_dystrophy_2": 10,
    "not_provided|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Retinal_dystrophy|Stargardt_disease_4|Retinitis_pigmentosa_41": 1,
    "Macular_dystrophy|Retinal_dystrophy|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Cone-rod_dystrophy_12|Retinitis_pigmentosa_41|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2": 1,
    "Retinitis_pigmentosa_41|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|not_provided": 1,
    "Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinitis_pigmentosa_41": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_12|PROM1-related_disorder|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Retinitis_pigmentosa_41|not_provided|Cone-rod_dystrophy": 1,
    "Retinal_dystrophy|not_specified|not_provided|PROM1-related_disorder|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Stargardt_disease_4": 1,
    "Stargardt_disease|Retinal_dystrophy|Retinitis_pigmentosa_41|Leber_congenital_amaurosis|not_provided": 1,
    "Stargardt_disease_4": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Stargardt_disease_4|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|not_provided": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_12": 1,
    "Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy_12|Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2": 1,
    "not_provided|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa|Stargardt_disease_4": 1,
    "Retinitis_pigmentosa|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|PROM1-related_disorder|not_specified|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 2,
    "not_provided|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12": 1,
    "not_provided|PROM1-related_disorder|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy|Cone-rod_dystrophy_12": 1,
    "Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinitis_pigmentosa_41|Retinitis_pigmentosa|not_provided": 2,
    "not_provided|Retinitis_pigmentosa_41|Retinal_dystrophy|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Retinitis_pigmentosa_41|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4": 1,
    "not_provided|Retinitis_pigmentosa_41|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Stargardt_disease_4": 1,
    "Retinitis_pigmentosa_41|Retinal_dystrophy|not_provided": 1,
    "Stargardt_disease_4|not_specified": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Cone-rod_dystrophy_12|Retinitis_pigmentosa_41|Stargardt_disease_4|Retinal_macular_dystrophy_type_2": 1,
    "Cone-rod_dystrophy_12|Stargardt_disease_4|Retinal_macular_dystrophy_type_2|Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinitis_pigmentosa_41": 1,
    "not_provided|Retinitis_pigmentosa_41|Cone-rod_dystrophy_12|Leber_congenital_amaurosis_1": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Stargardt_disease_4": 1,
    "not_specified|not_provided|Retinal_macular_dystrophy_type_2|Cone-rod_dystrophy_12|Retinitis_pigmentosa|Stargardt_disease_4": 1,
    "Retinal_macular_dystrophy_type_2|Stargardt_disease_4|not_specified|Cone-rod_dystrophy_12|Retinitis_pigmentosa|not_provided": 1,
    "Cone-rod_dystrophy_12|Retinal_macular_dystrophy_type_2|Stargardt_disease_4|Retinitis_pigmentosa_41|Retinitis_pigmentosa": 1,
    "Complex_lethal_osteochondrodysplasia": 5,
    "TAPT1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Complex_lethal_osteochondrodysplasia|not_provided": 1,
    "not_provided|TAPT1-related_disorder": 3,
    "TAPT1-related_disorder": 2,
    "not_provided|Complex_lethal_osteochondrodysplasia": 3,
    "Short_stature|Scoliosis|Recurrent_fractures|Reduced_bone_mineral_density|Abnormal_long_bone_morphology": 1,
    "not_provided|Complex_lethal_osteochondrodysplasia|Inborn_genetic_diseases": 1,
    "Dihydropteridine_reductase_deficiency": 295,
    "not_provided|Dihydropteridine_reductase_deficiency": 16,
    "BH4-Deficient_Hyperphenylalaninemia|not_provided": 4,
    "BH4-Deficient_Hyperphenylalaninemia": 8,
    "QDPR-related_disorder": 1,
    "Dihydropteridine_reductase_deficiency|Inborn_genetic_diseases": 8,
    "not_specified|Dihydropteridine_reductase_deficiency": 1,
    "Dihydropteridine_reductase_deficiency|not_specified": 1,
    "Dihydropteridine_reductase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Dihydropteridine_reductase_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|BH4-Deficient_Hyperphenylalaninemia|Dihydropteridine_reductase_deficiency": 1,
    "Dihydropteridine_reductase_deficiency|QDPR-related_disorder": 3,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Dihydropteridine_reductase_deficiency": 1,
    "not_specified|Dihydropteridine_reductase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Dihydropteridine_reductase_deficiency": 3,
    "Inborn_genetic_diseases|not_provided|Dihydropteridine_reductase_deficiency": 1,
    "not_provided|not_specified|Dihydropteridine_reductase_deficiency": 1,
    "not_provided|Dihydropteridine_reductase_deficiency|not_specified": 1,
    "Dihydropteridine_reductase_deficiency|Hyperphenylalaninemia_due_to_tetrahydrobiopterin_deficiency": 1,
    "QDPR-related_disorder|Dihydropteridine_reductase_deficiency": 1,
    "not_provided|BH4-Deficient_Hyperphenylalaninemia|Dihydropteridine_reductase_deficiency": 2,
    "not_specified|CLRN2-related_disorder": 2,
    "Hearing_loss|_autosomal_recessive_117": 2,
    "CLRN2-related_disorder": 1,
    "SLIT2-related_disorder|not_provided": 16,
    "SLIT2-related_disorder": 22,
    "not_provided|SLIT2-related_disorder": 9,
    "SLIT2-related_disorder|not_provided|not_specified": 1,
    "SLIT2-related_disorder|not_specified": 1,
    "KCNIP4-related_disorder": 3,
    "not_provided|ADGRA3-related_disorder": 10,
    "ADGRA3-related_disorder": 3,
    "Retinal_dystrophy|ADGRA3-related_disorder|not_provided": 1,
    "ADGRA3-related_disorder|not_provided": 7,
    "Optic_atrophy|not_specified|ADGRA3-related_disorder|not_provided|Retinal_dystrophy": 1,
    "not_specified|not_provided|ADGRA3-related_disorder": 1,
    "Retinal_dystrophy|not_provided|ADGRA3-related_disorder": 1,
    "PPARGC1A-related_disorder": 14,
    "PPARGC1A-related_disorder|not_provided": 1,
    "not_provided|PPARGC1A-related_disorder": 4,
    "Gray_matter_heterotopia|Intellectual_disability|_moderate|Abnormal_facial_shape|Patent_ductus_arteriosus|Delayed_speech_and_language_development|Periventricular_heterotopia|Seizure|Cerebral_white_matter_hypoplasia": 1,
    "SOD3-related_disorder": 4,
    "SOD3-related_disorder|not_provided": 2,
    "not_provided|SOD3-related_disorder": 1,
    "SOD3-related_disorder|Superoxide_dismutase|_elevated_extracellular": 1,
    "Pontocerebellar_hypoplasia_type_2D": 112,
    "not_provided|Pontocerebellar_hypoplasia_type_2D": 24,
    "Pontocerebellar_hypoplasia_type_2D|not_provided": 18,
    "SEPSECS-related_disorder": 2,
    "not_provided|Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_2D": 2,
    "not_provided|not_specified|Pontocerebellar_hypoplasia_type_2D": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Spastic_ataxia|Pontocerebellar_hypoplasia_type_2D": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_2D": 3,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia_type_2D": 4,
    "not_specified|Pontocerebellar_hypoplasia_type_2D|not_provided": 2,
    "Pontocerebellar_hypoplasia_type_2D|SEPSECS-related_disorder|not_provided": 1,
    "Elliptical_nystagmus|Progressive_limb_weakness|Cerebellar_ataxia|Neurodegeneration|Spastic_diplegia|Dysarthria": 1,
    "Pontocerebellar_hypoplasia_type_2D|not_provided|SEPSECS-related_disorder": 2,
    "not_provided|Pontocerebellar_hypoplasia_type_2D|not_specified": 1,
    "SEPSECS-related_disorder|Pontocerebellar_hypoplasia_type_2D|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_2D": 2,
    "Pontocerebellar_hypoplasia_type_2D|Inborn_genetic_diseases|not_provided": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Pontocerebellar_hypoplasia_type_2D": 1,
    "Pontocerebellar_hypoplasia_type_2D|not_specified": 3,
    "Pontocerebellar_hypoplasia_type_2D|Congenital_cerebellar_hypoplasia|Arthrogryposis_multiplex_congenita|Kyphosis|Spinal_rigidity|Cerebral_hypoplasia|Seizure|Severe_global_developmental_delay": 1,
    "not_provided|SEPSECS-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_2D|not_specified|not_provided": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_2D|not_provided|Neurodevelopmental_abnormality": 1,
    "PULMONARY_ALVEOLAR_MICROLITHIASIS": 14,
    "SLC34A2-related_disorder|not_provided": 3,
    "SLC34A2-related_disorder": 4,
    "not_provided|PULMONARY_ALVEOLAR_MICROLITHIASIS": 2,
    "PULMONARY_ALVEOLAR_MICROLITHIASIS|not_provided": 2,
    "not_provided|SLC34A2-related_disorder|PULMONARY_ALVEOLAR_MICROLITHIASIS": 1,
    "not_provided|SLC34A2-related_disorder": 1,
    "PULMONARY_ALVEOLAR_MICROLITHIASIS|not_provided|SLC34A2-related_disorder": 1,
    "PULMONARY_ALVEOLAR_MICROLITHIASIS|Inborn_genetic_diseases": 1,
    "PULMONARY_ALVEOLAR_MICROLITHIASIS|not_provided|not_specified": 1,
    "RBPJ-related_disorder": 6,
    "Adams-Oliver_syndrome_3": 7,
    "Combined_immunodeficiency_with_skin_granulomas": 19,
    "Adams-Oliver_syndrome_3|not_provided": 1,
    "Adams-Oliver_syndrome_3|RBPJ-related_disorder": 1,
    "Type_2_diabetes_mellitus|Adams-Oliver_syndrome_3": 1,
    "not_provided|RBPJ-related_disorder": 1,
    "RBPJ-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Adams-Oliver_syndrome_3": 1,
    "CHOLECYSTOKININ_A_RECEPTOR_POLYMORPHISM|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis|Muscular_dystrophy": 1,
    "not_provided|DTHD1-related_disorder": 8,
    "DTHD1-related_disorder": 2,
    "LCAT_deficiency": 15,
    "TBC1D1-related_disorder|not_provided": 3,
    "TBC1D1-related_disorder": 36,
    "Inborn_genetic_diseases|TBC1D1-related_disorder": 3,
    "Inborn_genetic_diseases|TBC1D1-related_disorder|not_provided": 1,
    "Non-syndromic_renal_or_urinary_tract_malformation|Inborn_genetic_diseases": 1,
    "not_provided|TBC1D1-related_disorder": 2,
    "not_specified|TBC1D1-related_disorder": 1,
    "TLR1-related_disorder|not_provided": 2,
    "Leprosy|_susceptibility_to|_1|Leprosy|_protection_against|TLR1-related_disorder": 1,
    "TLR1-related_disorder": 14,
    "not_provided|TLR1-related_disorder": 2,
    "Leprosy|_susceptibility_to|_5|TLR1-related_disorder": 1,
    "Jeune_thoracic_dystrophy|Cranioectodermal_dysplasia": 2,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|not_specified|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|not_provided|Senior-Loken_syndrome_8|not_specified": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 345,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 337,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 19,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4": 4,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 10,
    "Retinal_dystrophy|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_5": 2,
    "Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13": 74,
    "Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|WDR19-related_disorder": 1,
    "Cranioectodermal_dysplasia_4|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "Cranioectodermal_dysplasia_4": 6,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Nephronophthisis_13": 2,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4": 2,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided": 7,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5": 11,
    "Senior-Loken_syndrome_8": 7,
    "Inborn_genetic_diseases|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13": 2,
    "not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 4,
    "not_provided|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 7,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 2,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|WDR19-related_disorder": 2,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Retinal_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 5,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 4,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|WDR19-related_disorder|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Nephronophthisis_13": 1,
    "not_provided|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|WDR19-related_disorder|not_specified": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 10,
    "Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 8,
    "WDR19-related_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 2,
    "Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Cranioectodermal_dysplasia_4|not_specified|Spermatogenic_failure_72|Nephronophthisis_13": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|WDR19-related_disorder|not_provided|Cranioectodermal_dysplasia_4": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Inborn_genetic_diseases|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|not_provided|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|WDR19-related_disorder": 3,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Nephronophthisis_13|not_provided|Retinal_dystrophy": 1,
    "Senior-Loken_syndrome_8|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 2,
    "Nephronophthisis_13": 11,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72|WDR19-related_disorder|Connective_tissue_disorder": 2,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Inborn_genetic_diseases": 14,
    "Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4": 5,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|WDR19-related_disorder|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Senior-Loken_syndrome_8|Inborn_genetic_diseases": 2,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Jeune_thoracic_dystrophy|Spermatogenic_failure_72|WDR19-related_disorder|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Jeune_thoracic_dystrophy": 2,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 8,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_4|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|not_specified|Senior-Loken_syndrome_8|not_provided": 2,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Connective_tissue_disorder|not_provided|Cranioectodermal_dysplasia_4|Nephronophthisis_13|not_specified": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_specified|not_provided": 2,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 2,
    "Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 3,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Inborn_genetic_diseases|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|WDR19-related_disorder": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Retinal_dystrophy|not_provided|Intellectual_disability": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_provided": 5,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Retinal_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Inborn_genetic_diseases|not_provided": 1,
    "WDR19-related_disorder|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|not_provided": 1,
    "Jeune_thoracic_dystrophy|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia": 1,
    "Cranioectodermal_dysplasia_4|WDR19-related_disorder|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_provided|not_specified|Cranioectodermal_dysplasia_4": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Cranioectodermal_dysplasia": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Jeune_thoracic_dystrophy|Connective_tissue_disorder|Cranioectodermal_dysplasia": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 3,
    "Cranioectodermal_dysplasia_4|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Connective_tissue_disorder|Senior-Loken_syndrome_8|not_provided|not_specified": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|WDR19-related_disorder|Cranioectodermal_dysplasia_4": 1,
    "Spermatogenic_failure_72|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|WDR19-related_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Nephronophthisis_13|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Inborn_genetic_diseases|not_provided": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Inborn_genetic_diseases": 2,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Senior-Loken_syndrome_8": 5,
    "WDR19-related_disorder|Spermatogenic_failure_72|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Inborn_genetic_diseases|not_provided": 1,
    "Senior-Loken_syndrome_8|Cranioectodermal_dysplasia": 1,
    "Saldino-Mainzer_syndrome|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5": 1,
    "Stargardt-like_macular_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Cone_dystrophy|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 2,
    "Nephronophthisis_13|not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Senior-Loken_syndrome_8|WDR19-related_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Jeune_thoracic_dystrophy": 2,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Inborn_genetic_diseases": 2,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Nephronophthisis_13": 2,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_specified|Cranioectodermal_dysplasia_4": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Inborn_genetic_diseases|not_provided": 1,
    "Connective_tissue_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_specified|not_provided|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Cranioectodermal_dysplasia_4|Nephronophthisis_13|WDR19-related_disorder|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|not_provided|Connective_tissue_disorder|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|not_specified": 1,
    "Cranioectodermal_dysplasia|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4": 1,
    "not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_specified": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72": 4,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 4,
    "Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Senior-Loken_syndrome_8": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|WDR19-related_disorder|not_provided": 1,
    "Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|not_provided": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Inborn_genetic_diseases|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_provided|Cranioectodermal_dysplasia_4|Nephronophthisis_13|not_specified": 1,
    "WDR19-related_disorder": 2,
    "Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72|not_provided": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "not_provided|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|not_provided": 1,
    "Renal_dysplasia_and_retinal_aplasia|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Connective_tissue_disorder|not_provided|WDR19-related_disorder": 1,
    "Senior-Loken_syndrome_8|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|not_specified|not_provided": 1,
    "not_specified|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Senior-Loken_syndrome_8|Connective_tissue_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72|Senior-Loken_syndrome_8": 1,
    "Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Inborn_genetic_diseases|Nephronophthisis|not_provided": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4": 1,
    "Inborn_genetic_diseases|Spermatogenic_failure_72|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 2,
    "not_specified|not_provided|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Jeune_thoracic_dystrophy|not_provided|Cranioectodermal_dysplasia|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 1,
    "not_provided|WDR19-related_disorder|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "WDR19-related_disorder|not_provided|Inborn_genetic_diseases|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "WDR19-related_disorder|not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4": 1,
    "Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Inborn_genetic_diseases": 1,
    "WDR19-related_disorder|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Cranioectodermal_dysplasia_4": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|WDR19-related_disorder|not_specified|not_provided|Cranioectodermal_dysplasia_4": 1,
    "Inborn_genetic_diseases|not_provided|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Inborn_genetic_diseases": 6,
    "Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4": 1,
    "WDR19-related_disorder|not_provided|not_specified|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|WDR19-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "Spermatogenic_failure_72|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Craniosynostosis_syndrome|not_provided": 1,
    "Saldino-Mainzer_syndrome|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|WDR19-related_disorder": 1,
    "Retinal_dystrophy|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 2,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Inborn_genetic_diseases": 1,
    "WDR19-related_disorder|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Inborn_genetic_diseases|Connective_tissue_disorder|not_specified|not_provided|Cranioectodermal_dysplasia_4": 1,
    "Nephronophthisis_13|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 1,
    "not_provided|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|WDR19-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis_13|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 1,
    "WDR19-related_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72": 1,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Senior-Loken_syndrome_8": 1,
    "Spermatogenic_failure_72|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13": 1,
    "WDR19-related_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_specified|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Connective_tissue_disorder|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13|not_provided": 1,
    "Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "Retinitis_pigmentosa|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Inborn_genetic_diseases|not_provided": 2,
    "Spermatogenic_failure_72|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "Senior-Loken_syndrome_8|Connective_tissue_disorder|Asphyxiating_thoracic_dystrophy_5|not_provided|Cranioectodermal_dysplasia_4|Nephronophthisis_13": 1,
    "Cranioectodermal_dysplasia_4|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|not_specified|not_provided|Senior-Loken_syndrome_8": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Renal_dysplasia_and_retinal_aplasia|not_provided|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Connective_tissue_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_specified|not_provided|Cranioectodermal_dysplasia_4": 1,
    "Cranioectodermal_dysplasia_4|Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|not_specified|Connective_tissue_disorder|Senior-Loken_syndrome_8|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_specified|Cranioectodermal_dysplasia_4|Nephronophthisis_13": 1,
    "WDR19-related_disorder|not_provided|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_8|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Retinal_dystrophy|Cranioectodermal_dysplasia_4": 1,
    "Inborn_genetic_diseases|not_provided|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Nephronophthisis_13": 1,
    "Jeune_thoracic_dystrophy|Connective_tissue_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia": 1,
    "Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72|Connective_tissue_disorder": 1,
    "Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|not_specified|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Inborn_genetic_diseases|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|not_specified": 1,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13": 1,
    "Retinitis_pigmentosa|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72": 1,
    "Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 1,
    "Type_IV_short_rib_polydactyly_syndrome|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Spermatogenic_failure_72": 1,
    "Nephronophthisis_13|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Senior-Loken_syndrome_8|WDR19-related_disorder|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Senior-Loken_syndrome_8|Cranioectodermal_dysplasia_4|Inborn_genetic_diseases": 1,
    "Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Senior-Loken_syndrome_8|not_provided|Leber_congenital_amaurosis|WDR19-related_disorder|Cranioectodermal_dysplasia": 1,
    "Connective_tissue_disorder|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Jeune_thoracic_dystrophy|not_provided|Nephronophthisis_13": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Spermatogenic_failure_72|Cranioectodermal_dysplasia_4": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|Nephronophthisis_13|Spermatogenic_failure_72|Senior-Loken_syndrome_8": 1,
    "Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "WDR19-related_disorder|not_provided|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8": 1,
    "WDR19-related_disorder|Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4|not_provided": 1,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Spermatogenic_failure_72|Senior-Loken_syndrome_8|Jeune_thoracic_dystrophy": 1,
    "WDR19-related_disorder|Bardet-Biedl_syndrome|not_provided|Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "Spermatogenic_failure_72": 1,
    "WDR19-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|not_provided|Spermatogenic_failure_72|Nephronophthisis_13|Cranioectodermal_dysplasia_4": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 1,
    "Retinal_dystrophy|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5": 1,
    "Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Cranioectodermal_dysplasia_4|not_specified": 1,
    "Inborn_genetic_diseases|Spermatogenic_failure_72|Asphyxiating_thoracic_dystrophy_5|Nephronophthisis_13|Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8": 1,
    "Asphyxiating_thoracic_dystrophy_5|Senior-Loken_syndrome_8|Retinal_dystrophy": 1,
    "Cranioectodermal_dysplasia_4|Senior-Loken_syndrome_8|Asphyxiating_thoracic_dystrophy_5|Spermatogenic_failure_72|Nephronophthisis_13": 1,
    "Cranioectodermal_dysplasia_4|Asphyxiating_thoracic_dystrophy_5|not_provided": 1,
    "not_provided|RFC1-related_disorder": 3,
    "Cerebellar_ataxia_with_neuropathy_and_bilateral_vestibular_areflexia_syndrome": 11,
    "not_provided|Cerebellar_ataxia_with_neuropathy_and_bilateral_vestibular_areflexia_syndrome": 4,
    "Cerebellar_ataxia_with_neuropathy_and_bilateral_vestibular_areflexia_syndrome|not_provided|RFC1-related_disorder": 1,
    "RFC1-related_disorder": 5,
    "RFC1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|RFC1-related_disorder": 1,
    "RFC1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|KLB-related_disorder": 9,
    "KLB-related_disorder": 3,
    "Ocular_motility_disease": 2,
    "KLB-related_disorder|not_provided": 2,
    "RPL9-related_disorder|not_provided": 1,
    "not_provided|LIAS-related_disorder": 1,
    "Lipoic_acid_synthetase_deficiency": 283,
    "LIAS-related_disorder|Lipoic_acid_synthetase_deficiency|not_specified": 1,
    "not_provided|Lipoic_acid_synthetase_deficiency|Inborn_genetic_diseases": 1,
    "Lipoic_acid_synthetase_deficiency|Inborn_genetic_diseases": 8,
    "not_provided|Lipoic_acid_synthetase_deficiency": 23,
    "Inborn_genetic_diseases|Lipoic_acid_synthetase_deficiency": 7,
    "not_provided|Lipoic_acid_synthetase_deficiency|not_specified": 1,
    "not_provided|LIAS-related_disorder|Lipoic_acid_synthetase_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Lipoic_acid_synthetase_deficiency": 3,
    "Lipoic_acid_synthetase_deficiency|not_provided": 8,
    "not_specified|not_provided|Lipoic_acid_synthetase_deficiency": 2,
    "Lipoic_acid_synthetase_deficiency|not_specified|not_provided": 3,
    "not_specified|Lipoic_acid_synthetase_deficiency": 2,
    "Lipoic_acid_synthetase_deficiency|not_specified": 1,
    "LIAS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Lipoic_acid_synthetase_deficiency": 1,
    "not_provided|LIAS-related_disorder|Lipoic_acid_synthetase_deficiency": 2,
    "LIAS-related_disorder|not_provided|Lipoic_acid_synthetase_deficiency": 1,
    "LIAS-related_disorder|Lipoic_acid_synthetase_deficiency": 1,
    "Developmental_and_epileptic_encephalopathy|_84": 12,
    "UGDH-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_84|Epileptic_encephalopathy": 5,
    "Developmental_and_epileptic_encephalopathy|_84|not_provided": 1,
    "not_specified|not_provided|UGDH-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_84|Epileptic_encephalopathy|UGDH-related_disorder": 1,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_84|West_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_84|UGDH-related_disorder|Epileptic_encephalopathy": 1,
    "PDS5A-related_disorder": 2,
    "RHOH-related_disorder": 1,
    "T-cell_immunodeficiency_with_epidermodysplasia_verruciformis": 69,
    "T-cell_immunodeficiency_with_epidermodysplasia_verruciformis|RHOH-related_disorder": 2,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_4": 2,
    "not_provided|T-cell_immunodeficiency_with_epidermodysplasia_verruciformis|Epidermodysplasia_verruciformis|_susceptibility_to|_4": 1,
    "T-cell_immunodeficiency_with_epidermodysplasia_verruciformis|not_provided": 1,
    "T-cell_immunodeficiency_with_epidermodysplasia_verruciformis|not_specified": 2,
    "not_provided|T-cell_immunodeficiency_with_epidermodysplasia_verruciformis": 1,
    "Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "Parkinson_disease_5|_autosomal_dominant|_susceptibility_to": 17,
    "not_provided|Parkinson_disease_5|_autosomal_dominant|_susceptibility_to": 9,
    "not_provided|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome": 1,
    "UCHL1-related_disorder": 4,
    "Spastic_paraplegia_79A|_autosomal_dominant|_with_ataxia": 10,
    "Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|not_provided|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome": 1,
    "not_provided|Spastic_paraplegia_79A|_autosomal_dominant|_with_ataxia": 2,
    "Spastic_paraplegia_79A|_autosomal_dominant|_with_ataxia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Parkinson_disease_5|_autosomal_dominant|_susceptibility_to": 1,
    "Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome|Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "not_provided|UCHL1-related_disorder": 2,
    "Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome": 3,
    "not_provided|not_specified|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome": 1,
    "Parkinson_Disease|_Dominant|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome|Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|not_provided": 1,
    "Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|UCHL1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|UCHL1-related_disorder": 1,
    "Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome|Parkinson_disease_5|_autosomal_dominant|_susceptibility_to": 1,
    "Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome|not_provided": 1,
    "Parkinson_disease_5|_autosomal_dominant|_susceptibility_to|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome": 1,
    "Congenital_central_hypoventilation|Neuroblastoma|_susceptibility_to|_2": 10,
    "not_provided|Congenital_central_hypoventilation|Neuroblastoma|_susceptibility_to|_2": 1,
    "Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation": 25,
    "not_provided|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation": 5,
    "Neuroblastoma|Congenital_central_hypoventilation": 3,
    "not_provided|Neuroblastoma|Congenital_central_hypoventilation": 1,
    "Haddad_syndrome": 229,
    "Neuroblastoma|_susceptibility_to|_2": 9,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 177,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Haddad_syndrome": 19,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 167,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|PHOX2B-related_disorder|not_provided|Haddad_syndrome": 1,
    "Haddad_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2": 5,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome": 4,
    "Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome": 2,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|not_specified|not_provided|Haddad_syndrome|Congenital_central_hypoventilation": 1,
    "Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|not_provided": 1,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Neuroblastoma|_susceptibility_to|_2|not_provided|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Neuroblastoma|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation|Haddad_syndrome": 1,
    "not_provided|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 1,
    "Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Congenital_central_hypoventilation|Haddad_syndrome|PHOX2B-related_disorder|Neuroblastoma|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Congenital_central_hypoventilation": 1,
    "Haddad_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Haddad_syndrome|not_provided": 3,
    "not_provided|Haddad_syndrome": 4,
    "PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 1,
    "PHOX2B-related_disorder": 9,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|not_provided|Haddad_syndrome": 2,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2": 1,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease": 4,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Congenital_central_hypoventilation|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Congenital_central_hypoventilation|PHOX2B-related_disorder": 1,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Neuroblastoma|_susceptibility_to|_2|PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Haddad_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|not_provided": 3,
    "Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease": 3,
    "Hereditary_cancer-predisposing_syndrome|PHOX2B-related_disorder": 2,
    "not_provided|PHOX2B-related_disorder|Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease": 1,
    "Hereditary_cancer-predisposing_syndrome|PHOX2B-related_disorder|Congenital_central_hypoventilation": 1,
    "PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Haddad_syndrome": 1,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Congenital_central_hypoventilation": 7,
    "not_provided|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation|not_specified|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 7,
    "Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation|PHOX2B-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|PHOX2B-related_disorder|Haddad_syndrome|not_provided": 1,
    "PHOX2B-related_disorder|Haddad_syndrome|not_provided": 2,
    "Haddad_syndrome|PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|not_provided|Haddad_syndrome|Congenital_central_hypoventilation": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Haddad_syndrome|PHOX2B-related_disorder|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation": 1,
    "PHOX2B-related_disorder|not_provided|Congenital_central_hypoventilation": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Congenital_central_hypoventilation": 1,
    "Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Haddad_syndrome": 1,
    "Congenital_central_hypoventilation|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PHOX2B-related_disorder|Haddad_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Haddad_syndrome": 1,
    "PHOX2B-related_disorder|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Congenital_central_hypoventilation|not_specified|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2": 1,
    "not_provided|PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|PHOX2B-related_disorder": 1,
    "Haddad_syndrome|PHOX2B-related_disorder": 1,
    "Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|not_provided|Haddad_syndrome|Congenital_central_hypoventilation": 1,
    "Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation|PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation": 1,
    "Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|PHOX2B-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2": 4,
    "Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Hereditary_cancer-predisposing_syndrome|not_provided|Haddad_syndrome": 2,
    "Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Congenital_central_hypoventilation|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease-ganglioneuroblastoma_syndrome": 1,
    "Haddad_syndrome|PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Haddad_syndrome|PHOX2B-related_disorder|Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease": 1,
    "Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation|not_specified|not_provided|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2": 1,
    "not_provided|Congenital_central_hypoventilation": 2,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2": 2,
    "Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Congenital_central_hypoventilation|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Haddad_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_2": 1,
    "Predisposition_to_neuroblastoma|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Haddad_syndrome|Congenital_central_hypoventilation|Neuroblastoma|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation|Neuroblastoma|_susceptibility_to|_2|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|not_provided|Haddad_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation": 3,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation": 2,
    "Hirschsprung_disease-ganglioneuroblastoma_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Congenital_central_hypoventilation_syndrome|_with_or_without_Hirschsprung_disease": 1,
    "PHOX2B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Haddad_syndrome": 1,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|Haddad_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Haddad_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Neuroblastoma|_susceptibility_to|_2": 1,
    "Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease": 1,
    "PHOX2B-related_disorder|Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|Congenital_central_hypoventilation": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation|Neuroblastoma|_susceptibility_to|_2|Haddad_syndrome|PHOX2B-related_disorder": 1,
    "Congenital_central_hypoventilation|Haddad_syndrome": 1,
    "Neuroblastoma|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Haddad_syndrome|Neuroblastoma|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Psychomotor_regression-oculomotor_apraxia-movement_disorder-nephropathy_syndrome": 6,
    "Inborn_genetic_diseases|Psychomotor_regression-oculomotor_apraxia-movement_disorder-nephropathy_syndrome|not_provided": 1,
    "not_provided|SLC30A9-related_disorder": 1,
    "SLC30A9-related_disorder": 2,
    "Psychomotor_regression-oculomotor_apraxia-movement_disorder-nephropathy_syndrome|Inborn_genetic_diseases": 1,
    "Psychomotor_regression-oculomotor_apraxia-movement_disorder-nephropathy_syndrome": 11,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_25": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_25": 5,
    "GRXCR1-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25": 15,
    "not_provided|GRXCR1-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25|Hearing_loss|_autosomal_recessive": 1,
    "GRXCR1-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_25": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_25": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_25": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_25|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25|not_provided|GRXCR1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_25": 1,
    "GRXCR1-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_25|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_25|not_specified|GRXCR1-related_disorder": 1,
    "GUF1-related_disorder|not_provided": 7,
    "Developmental_and_epileptic_encephalopathy|_40|not_provided": 6,
    "not_provided|GUF1-related_disorder": 9,
    "not_provided|Developmental_and_epileptic_encephalopathy|_40": 2,
    "Developmental_and_epileptic_encephalopathy|_40": 3,
    "GUF1-related_disorder": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_40": 1,
    "Developmental_and_epileptic_encephalopathy|_40|not_provided|GUF1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_40|not_provided|not_specified": 1,
    "GABRA2-related_disorder": 3,
    "not_provided|GABRA2-related_disorder": 6,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_78|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_78": 18,
    "GABRA2-related_disorder|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_78|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_78|Alcohol_dependence": 1,
    "Developmental_and_epileptic_encephalopathy|_78|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_78": 3,
    "Alcoholism|_susceptibility_to": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_78|Alcohol_dependence": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_78": 1,
    "GABRA4-related_Epileptic_and_Neurodevelopmental_Disorder": 1,
    "GABRA4-related_disorder": 1,
    "not_provided|GABRA4-associated_disorder": 1,
    "GABRA4-related_developmental_and_epileptic_encephalopathy": 1,
    "GABRB1-related_disorder": 2,
    "GABRB1-related_disorder|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_45": 11,
    "GABRB1-related_disorder|not_provided": 4,
    "not_specified|Developmental_and_epileptic_encephalopathy|_45": 1,
    "not_provided|GABRB1-related_disorder": 5,
    "Developmental_and_epileptic_encephalopathy|_45|not_provided": 5,
    "not_provided|Developmental_and_epileptic_encephalopathy|_45": 2,
    "Developmental_and_epileptic_encephalopathy|_45|GABRB1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_45|not_specified|not_provided": 1,
    "CORIN-related_disorder": 6,
    "CORIN-related_disorder|not_provided": 2,
    "not_specified|Preeclampsia/eclampsia_5|not_provided": 1,
    "Cardiomyopathy|_familial_hypertrophic|_30|_atrial": 1,
    "Preeclampsia/eclampsia_5": 3,
    "Atrial_fibrillation|Cardiomyopathy|Myocardial_fibrosis|Hypertensive_disorder|Cardiomyopathy|_familial_hypertrophic|_30|_atrial": 1,
    "Preeclampsia/eclampsia_5|not_provided": 1,
    "NFXL1-related_disorder": 15,
    "Structural_heart_defects_and_renal_anomalies_syndrome": 31,
    "Retinitis_pigmentosa_49": 16,
    "Retinitis_pigmentosa_49|not_provided": 8,
    "Retinitis_pigmentosa_49|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_49": 1,
    "not_provided|Retinitis_pigmentosa_49": 5,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_49|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_49|Retinitis_pigmentosa": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_49|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_49": 3,
    "Inborn_genetic_diseases|not_provided|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinal_dystrophy|CNGA1-related_disorder|not_provided": 1,
    "not_provided|CNGA1-related_disorder": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_49": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_49": 1,
    "Retinitis_pigmentosa_49|CNGA1-related_retinopathy|not_provided": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_49|Retinitis_pigmentosa": 1,
    "not_provided|Prostate_cancer": 9,
    "Retinal_dystrophy|Retinitis_pigmentosa_49|not_provided|CNGA1-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa_49|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Retinitis_pigmentosa_49|not_provided": 1,
    "CNGA1-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_49|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_49": 1,
    "CNGA1-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|CNGA1-related_retinopathy": 1,
    "CNGA1-related_disorder|Macular_dystrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_49|Retinitis_pigmentosa|Cone-rod_dystrophy|See_cases": 1,
    "See_cases|Retinitis_pigmentosa_49": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_49": 1,
    "CNGA1-related_disorder|Retinitis_pigmentosa_49|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|CNGA1-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_49": 1,
    "not_provided|Retinitis_pigmentosa_49|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "CNGA1-related_disorder": 3,
    "not_provided|Retinal_dystrophy|Optic_atrophy|CNGA1-related_disorder": 1,
    "FRYL-related_developmental_disorder": 4,
    "Pan-Chung-Bellen_syndrome|FRYL-related_developmental_disorder": 4,
    "Pan-Chung-Bellen_syndrome|not_provided|FRYL-related_developmental_disorder": 1,
    "Pan-Chung-Bellen_syndrome": 4,
    "not_specified|Pan-Chung-Bellen_syndrome": 1,
    "not_specified|FRYL-related_developmental_disorder": 1,
    "not_provided|Pan-Chung-Bellen_syndrome|FRYL-related_developmental_disorder": 1,
    "FRYL-associated_neurodevelopmental_disorder|FRYL-related_developmental_disorder": 1,
    "not_provided|FRYL-related_developmental_disorder": 1,
    "FRYL-related_disorder": 1,
    "FRYL-related_developmental_disorder|Pan-Chung-Bellen_syndrome|not_specified": 1,
    "Qualitative_or_quantitative_defects_of_beta-sarcoglycan|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan": 30,
    "Qualitative_or_quantitative_defects_of_beta-sarcoglycan": 30,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided|Qualitative_or_quantitative_defects_of_beta-sarcoglycan": 5,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 405,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 32,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_specified|Qualitative_or_quantitative_defects_of_beta-sarcoglycan": 1,
    "not_provided|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 3,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|not_provided|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Hypertrophic_cardiomyopathy": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Primary_dilated_cardiomyopathy|not_provided": 1,
    "not_provided|SGCB-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_provided": 22,
    "Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Autosomal_recessive_limb-girdle_muscular_dystrophy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Inborn_genetic_diseases": 3,
    "not_provided|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Qualitative_or_quantitative_defects_of_beta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Sialidosis|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Qualitative_or_quantitative_defects_of_beta-sarcoglycan": 1,
    "Inborn_genetic_diseases|not_specified|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|SGCB-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 3,
    "SGCB-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_provided|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Primary_dilated_cardiomyopathy": 1,
    "Inborn_genetic_diseases|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided|Limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Abnormality_of_the_musculature": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_specified": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2E|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Qualitative_or_quantitative_defects_of_beta-sarcoglycan": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_beta-sarcoglycan|not_specified": 1,
    "Qualitative_or_quantitative_defects_of_beta-sarcoglycan|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "CHIC2-related_disorder": 1,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_2": 2,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_2|not_provided": 2,
    "not_provided|Diencephalic-mesencephalic_junction_dysplasia_syndrome_2": 1,
    "GSX2-related_disorder": 2,
    "Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 41,
    "Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 30,
    "Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|not_provided": 7,
    "PDGFRA-related_disorder": 10,
    "not_provided|Gastrointestinal_stromal_tumor": 24,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor": 10,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 720,
    "Ovarian_cancer|not_provided|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 64,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 4,
    "Ovarian_cancer|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 6,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor": 9,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_specified|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome": 18,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|PDGFRA-related_disorder": 2,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 10,
    "Myeloproliferative_neoplasm|_unclassifiable|Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor": 6,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|PDGFRA-related_disorder|not_specified": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 26,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 4,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|PDGFRA-related_disorder|Ovarian_cancer|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder|Gastrointestinal_stromal_tumor": 9,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided|PDGFRA-related_disorder|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 3,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 3,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 10,
    "Gastrointestinal_stromal_tumor|not_provided|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Idiopathic_hypereosinophilic_syndrome|not_specified|Gastrointestinal_stromal_tumor": 1,
    "PDGFRA-related_disorder|Gastrointestinal_stromal_tumor": 2,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 4,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided": 39,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|PDGFRA-related_disorder": 5,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder": 5,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 15,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder|not_provided|Gastrointestinal_stromal_tumor": 2,
    "not_provided|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Lung_sarcomatoid_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome": 2,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 2,
    "not_provided|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome": 1,
    "Idiopathic_hypereosinophilic_syndrome|PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Idiopathic_hypereosinophilic_syndrome|not_provided|Gastrointestinal_stromal_tumor": 2,
    "Myeloproliferative_neoplasm|_unclassifiable|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|not_provided": 1,
    "not_provided|PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided|PDGFRA-related_disorder": 4,
    "Gastrointestinal_stromal_tumor|PDGFRA-related_disorder": 2,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor": 10,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 22,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|PDGFRA-related_disorder|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 29,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|PDGFRA-related_disorder|not_provided|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|PDGFRA-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 2,
    "PDGFRA-related_disorder|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 4,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Gastrointestinal_stromal_tumor|not_provided": 14,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Idiopathic_hypereosinophilic_syndrome|not_provided|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "PDGFRA-related_disorder|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 3,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 4,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder|not_provided": 1,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Gastrointestinal_stromal_tumor|Isolated_cleft_palate": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder|not_provided|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder|not_provided|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Idiopathic_hypereosinophilic_syndrome|PDGFRA-related_disorder|Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_specified": 1,
    "PDGFRA-related_disorder|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Idiopathic_hypereosinophilic_syndrome": 3,
    "PDGFRA-related_disorder|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|PDGFRA-related_disorder|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|Gastrointestinal_stromal_tumor": 3,
    "Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome": 6,
    "Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome|Isolated_cleft_palate": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor|PDGFRA-related_disorder": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|Gastrointestinal_stromal_tumor": 2,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Squamous_cell_lung_carcinoma|Carcinoma_of_colon|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Gastrointestinal_stromal_tumor": 4,
    "Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|not_specified|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastrointestinal_stromal_tumor|PDGFRA-related_disorder|not_specified": 1,
    "Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Hypereosinophilic_syndrome|_idiopathic|_resistant_to_imatinib": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor": 1,
    "Idiopathic_hypereosinophilic_syndrome": 2,
    "PDGFRA-related_disorder|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Ovarian_cancer": 1,
    "Hereditary_cancer|not_specified|Myeloproliferative_neoplasm|_unclassifiable|PDGFRA-related_disorder": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|PDGFRA-related_disorder": 1,
    "not_provided|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1,
    "not_provided|Gastrointestinal_stromal_tumor|PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "PDGFRA-related_disorder|not_specified|Gastrointestinal_stromal_tumor": 1,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_specified|not_provided": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 1,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor": 1,
    "PDGFRA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor": 1,
    "PDGFRA-related_disorder|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Ovarian_cancer|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|not_provided": 1,
    "PDGFRA-related_disorder|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Idiopathic_hypereosinophilic_syndrome": 1,
    "Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|PDGFRA-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Gastrointestinal_stromal_tumor": 3,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_cleft_palate|Gastrointestinal_stromal_tumor": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Hereditary_cancer-predisposing_syndrome|not_provided|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Idiopathic_hypereosinophilic_syndrome|Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal": 1,
    "Polyps|_multiple_and_recurrent_inflammatory_fibroid|_gastrointestinal|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|PDGFRA-related_disorder|Idiopathic_hypereosinophilic_syndrome": 1,
    "Idiopathic_hypereosinophilic_syndrome|not_provided|Gastrointestinal_stromal_tumor": 4,
    "not_provided|Idiopathic_hypereosinophilic_syndrome|Gastrointestinal_stromal_tumor": 2,
    "Gastrointestinal_stromal_tumor|not_provided|Idiopathic_hypereosinophilic_syndrome": 1,
    "Piebaldism|Gastrointestinal_stromal_tumor|Mastocytosis": 8,
    "Gastrointestinal_stromal_tumor|Piebaldism|Mastocytosis": 4,
    "Mastocytosis|Piebaldism|not_provided|Gastrointestinal_stromal_tumor|not_specified": 1,
    "KIT-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|KIT-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|KIT-related_disorder": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|KIT-related_disorder": 1,
    "Gastrointestinal_stromal_tumor|not_provided|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Piebaldism|Acute_myeloid_leukemia|Gastrointestinal_stromal_tumor|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis": 1,
    "Piebaldism|KIT-related_disorder|Mastocytosis|Gastrointestinal_stromal_tumor": 1,
    "not_provided|Gastrointestinal_stromal_tumor|not_specified|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Gastrointestinal_stromal_tumor|Malignant_tumor_of_testis": 1,
    "not_provided|Gastrointestinal_stromal_tumor|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 4,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 4,
    "not_specified|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Piebaldism|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Gastrointestinal_stromal_tumor": 2,
    "Hereditary_cancer-predisposing_syndrome|KIT-related_disorder|Gastrointestinal_stromal_tumor": 6,
    "KIT-related_disorder|Hereditary_skin_disorder|Piebaldism|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Malignant_tumor_of_testis|Mastocytosis|not_specified|not_provided": 1,
    "Gastrointestinal_stromal_tumor|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Piebaldism": 39,
    "not_specified|Gastrointestinal_stromal_tumor|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Piebaldism|Mastocytosis|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 3,
    "Hereditary_cancer-predisposing_syndrome|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Hereditary_cancer-predisposing_syndrome|Piebaldism|Gastrointestinal_stromal_tumor|Mastocytosis|Acute_myeloid_leukemia|Malignant_tumor_of_testis|not_provided": 2,
    "KIT-related_disorder|Gastrointestinal_stromal_tumor": 5,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|See_cases": 1,
    "Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 4,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 6,
    "Hereditary_cancer-predisposing_syndrome|Mastocytosis|Piebaldism|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Gastrointestinal_stromal_tumor|_familial|not_provided": 1,
    "Gastrointestinal_stromal_tumor|KIT-related_disorder": 6,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor": 3,
    "Gastrointestinal_stromal_tumor|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|Piebaldism|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis": 1,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Piebaldism|Cutaneous_mastocytosis|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Cutaneous_mastocytosis|Piebaldism": 1,
    "Acute_myeloid_leukemia|Gastrointestinal_stromal_tumor|Piebaldism|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided|KIT-related_disorder": 1,
    "Piebaldism|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome": 2,
    "Gastrointestinal_stromal_tumor|Germ_cell_tumor_of_testis|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Piebaldism|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastrointestinal_stromal_tumor|Germ_cell_tumor_of_testis|Acute_myeloid_leukemia|Piebaldism|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mastocytosis|Gastrointestinal_stromal_tumor|Gastrointestinal_stromal_tumor|_familial|Piebaldism": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|KIT-related_disorder|not_provided": 2,
    "Acute_myeloid_leukemia|Piebaldism|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Piebaldism|Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Piebaldism|not_provided|Mastocytosis|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Mastocytosis|not_provided|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 4,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Piebaldism|Acute_myeloid_leukemia": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided|Mastocytosis|KIT-related_disorder|Piebaldism": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Piebaldism|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis": 1,
    "Mastocytosis|Piebaldism|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Gastrointestinal_stromal_tumor": 1,
    "Mastocytosis|Piebaldism|Hereditary_cancer-predisposing_syndrome|KIT-related_disorder|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Mastocytosis|Piebaldism|Gastrointestinal_stromal_tumor": 1,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gastrointestinal_stromal_tumor|Mastocytosis|Piebaldism": 2,
    "Gastrointestinal_stromal_tumor|not_specified": 1,
    "Germ_cell_tumor_of_testis|Piebaldism|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|Mastocytosis|Piebaldism|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Gastrointestinal_stromal_tumor|Piebaldism|Mastocytosis|Hereditary_cancer-predisposing_syndrome": 1,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|KIT-related_disorder|not_provided": 1,
    "Gastrointestinal_stromal_tumor|not_provided|Hereditary_cancer-predisposing_syndrome|Mastocytosis|Piebaldism|Acute_myeloid_leukemia|Malignant_tumor_of_testis": 1,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Cutaneous_mastocytosis": 2,
    "Mastocytosis|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mastocytosis|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Piebaldism|not_provided": 1,
    "Lip_and_oral_cavity_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Hereditary_cancer-predisposing_syndrome|Piebaldism|Mastocytosis|Gastrointestinal_stromal_tumor|not_specified|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Mastocytosis": 1,
    "B_Lymphoblastic_Leukemia/Lymphoma_with_t(v%3B11q23.3)%3B_KMT2A_Rearranged|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|_familial": 1,
    "Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Gastrointestinal_stromal_tumor|_familial": 1,
    "Gastrointestinal_stromal_tumor|Piebaldism": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|KIT-related_disorder|Gastrointestinal_stromal_tumor": 2,
    "not_provided|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Piebaldism|_progressive": 1,
    "Mastocytosis|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Piebaldism|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Piebaldism|Hereditary_cancer-predisposing_syndrome": 2,
    "Gastrointestinal_stromal_tumor|Gastrointestinal_stromal_tumor|_familial": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|KIT-related_disorder|Ovarian_cancer|not_provided": 1,
    "Piebaldism|Cutaneous_mastocytosis|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome": 1,
    "Piebaldism|Gastrointestinal_stromal_tumor": 1,
    "Piebaldism|Gastrointestinal_stromal_tumor|Mastocytosis|Acute_myeloid_leukemia|Malignant_tumor_of_testis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Acute_myeloid_leukemia|Mastocytosis|Malignant_tumor_of_testis|Gastrointestinal_stromal_tumor|Piebaldism|Hereditary_cancer-predisposing_syndrome|KIT-related_disorder|not_provided": 1,
    "Acute_myeloid_leukemia|Gastrointestinal_stromal_tumor|Piebaldism|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mastocytosis|Gastrointestinal_stromal_tumor|not_provided|Piebaldism": 1,
    "Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Piebaldism|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Piebaldism|Cutaneous_mastocytosis|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis": 1,
    "not_specified|not_provided|Gastrointestinal_stromal_tumor": 1,
    "not_provided|Piebaldism|Gastrointestinal_stromal_tumor|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome": 1,
    "Piebaldism|Hereditary_cancer-predisposing_syndrome|Mastocytosis|KIT-related_disorder|Gastrointestinal_stromal_tumor": 1,
    "Piebaldism|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Gastrointestinal_stromal_tumor|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Piebaldism|Mastocytosis|not_provided": 1,
    "Gastrointestinal_stromal_tumor|Mastocytosis|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|KIT-related_disorder|Mastocytosis|Piebaldism|Gastrointestinal_stromal_tumor": 1,
    "Acute_myeloid_leukemia|Mastocytosis|Malignant_tumor_of_testis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Piebaldism_with_sensorineural_deafness": 1,
    "Mastocytosis|Piebaldism|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|not_specified": 1,
    "Dysgerminoma|Germ_cell_tumor_of_testis|not_provided": 1,
    "MASTOCYTOSIS|_CUTANEOUS_AND_SYSTEMIC|_SOMATIC|Acute_myeloid_leukemia|Gastrointestinal_stromal_tumor": 1,
    "Dysgerminoma|MAST_CELL_LEUKEMIA|_SOMATIC|MASTOCYTOSIS_WITH_ASSOCIATED_HEMATOLOGIC_DISORDER|_SOMATIC|MASTOCYTOSIS|_SYSTEMIC|_SOMATIC|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Gastrointestinal_stromal_tumor|Piebaldism|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis": 1,
    "KIT-related_disorder|Gastrointestinal_stromal_tumor|not_provided": 1,
    "MASTOCYTOSIS|_SYSTEMIC|_SOMATIC|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Piebaldism|Acute_myeloid_leukemia|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|KIT-related_disorder": 1,
    "Mastocytosis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Gastrointestinal_stromal_tumor|Piebaldism|Hereditary_cancer-predisposing_syndrome|Mastocytosis|not_specified|not_provided": 1,
    "Squamous_cell_lung_carcinoma|not_provided|Hereditary_cancer": 1,
    "Piebaldism|Acute_myeloid_leukemia|Gastrointestinal_stromal_tumor|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Acute_myeloid_leukemia|Cutaneous_mastocytosis|Germ_cell_tumor_of_testis|Gastrointestinal_stromal_tumor|Piebaldism|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Gastrointestinal_stromal_tumor|Cutaneous_mastocytosis|Acute_myeloid_leukemia|Piebaldism|Germ_cell_tumor_of_testis": 1,
    "Piebaldism|Mastocytosis|KIT-related_disorder|Gastrointestinal_stromal_tumor": 1,
    "KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism": 1,
    "Mastocytosis|Acute_myeloid_leukemia|Gastrointestinal_stromal_tumor|Piebaldism|Malignant_tumor_of_testis|Germ_cell_tumor_of_testis|Cutaneous_mastocytosis|KIT-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Mastocytosis|Piebaldism": 1,
    "Hereditary_cancer-predisposing_syndrome|KIT-related_disorder|not_provided|Gastrointestinal_stromal_tumor|Piebaldism|Mastocytosis": 1,
    "Piebaldism|Gastrointestinal_stromal_tumor|Germ_cell_tumor_of_testis|Acute_myeloid_leukemia|Cutaneous_mastocytosis|Hereditary_cancer-predisposing_syndrome|not_provided|Mastocytosis": 1,
    "Dysgerminoma": 2,
    "Acute_myeloid_leukemia|Mastocytosis|Malignant_tumor_of_testis|Gastrointestinal_stromal_tumor|Piebaldism|Hereditary_cancer-predisposing_syndrome": 1,
    "Cutaneous_mastocytosis|Acute_myeloid_leukemia|Piebaldism|Germ_cell_tumor_of_testis|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Systemic_mast_cell_disease": 1,
    "Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Mastocytosis|Piebaldism|Acute_myeloid_leukemia|Malignant_tumor_of_testis|Regorafenib_response": 1,
    "Acute_myeloid_leukemia|Mastocytosis|Malignant_tumor_of_testis|Gastrointestinal_stromal_tumor|Piebaldism|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mastocytosis|Piebaldism|Gastrointestinal_stromal_tumor": 15,
    "not_provided|Gastrointestinal_stromal_tumor|Piebaldism|Mastocytosis": 1,
    "not_provided|Mastocytosis|Piebaldism|Gastrointestinal_stromal_tumor": 4,
    "not_provided|Gastrointestinal_stromal_tumor|Mastocytosis|Piebaldism": 1,
    "Mastocytosis|Gastrointestinal_stromal_tumor|Piebaldism|not_provided": 1,
    "Piebaldism|Mastocytosis|Gastrointestinal_stromal_tumor": 6,
    "Gastrointestinal_stromal_tumor|not_provided|Mastocytosis|Piebaldism": 1,
    "Mastocytosis|not_provided|Piebaldism|Gastrointestinal_stromal_tumor": 1,
    "KDR-related_disorder": 9,
    "not_provided|KDR-related_disorder": 4,
    "Capillary_infantile_hemangioma|not_provided|not_specified": 1,
    "Capillary_infantile_hemangioma|not_specified": 3,
    "not_specified|Capillary_infantile_hemangioma": 1,
    "Tetralogy_of_Fallot": 30,
    "Tufted_angioma_of_skin|High_myopia|not_provided|Capillary_infantile_hemangioma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|not_provided|not_specified": 1,
    "Capillary_infantile_hemangioma|not_specified|not_provided": 1,
    "KDR-related_disorder|not_specified": 2,
    "Tufted_angioma_of_skin|Capillary_infantile_hemangioma": 1,
    "not_provided|not_specified|Capillary_infantile_hemangioma": 1,
    "Premature_ovarian_failure|not_specified": 2,
    "not_specified|KDR-related_disorder": 1,
    "not_specified|SRD5A3-congenital_disorder_of_glycosylation": 4,
    "SRD5A3-congenital_disorder_of_glycosylation|Kahrizi_syndrome": 3,
    "not_provided|SRD5A3-congenital_disorder_of_glycosylation": 7,
    "not_provided|SRD5A3-congenital_disorder_of_glycosylation|not_specified": 1,
    "SRD5A3-congenital_disorder_of_glycosylation|not_provided": 15,
    "not_provided|SRD5A3-related_disorder|SRD5A3-congenital_disorder_of_glycosylation|not_specified": 1,
    "SRD5A3-related_disorder|Autism|Cone_dystrophy|Global_developmental_delay|not_provided|Kahrizi_syndrome|SRD5A3-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|Abnormality_of_the_nervous_system": 1,
    "SRD5A3-related_disorder|not_provided|SRD5A3-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|SRD5A3-congenital_disorder_of_glycosylation": 6,
    "Kahrizi_syndrome": 1,
    "Congenital_cerebellar_hypoplasia|Inborn_genetic_diseases|SRD5A3-congenital_disorder_of_glycosylation": 1,
    "SRD5A3-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 4,
    "Abnormality_of_the_nervous_system|SRD5A3-congenital_disorder_of_glycosylation": 1,
    "SRD5A3-related_disorder": 1,
    "Kahrizi_syndrome|SRD5A3-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|SRD5A3-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "not_specified|not_provided|SRD5A3-congenital_disorder_of_glycosylation": 1,
    "not_provided|Congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_provided|Abnormal_optic_nerve_morphology": 1,
    "SRD5A3-congenital_disorder_of_glycosylation|SRD5A3-related_disorder": 1,
    "SRD5A3-related_disorder|SRD5A3-congenital_disorder_of_glycosylation": 1,
    "Kahrizi_syndrome|SRD5A3-congenital_disorder_of_glycosylation": 1,
    "SRD5A3-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "not_provided|Kahrizi_syndrome|SRD5A3-congenital_disorder_of_glycosylation|Hemangioma|Low-set_ears|Generalized_hypotonia|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_disorder_of_glycosylation": 30,
    "TMEM165-congenital_disorder_of_glycosylation|not_provided": 4,
    "TMEM165-congenital_disorder_of_glycosylation": 107,
    "not_specified|TMEM165-congenital_disorder_of_glycosylation|TMEM165-related_disorder": 1,
    "TMEM165-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "not_specified|TMEM165-congenital_disorder_of_glycosylation": 7,
    "not_specified|TMEM165-congenital_disorder_of_glycosylation|not_provided": 1,
    "TMEM165-related_disorder|not_provided|TMEM165-congenital_disorder_of_glycosylation": 1,
    "not_provided|TMEM165-congenital_disorder_of_glycosylation": 3,
    "TMEM165-related_disorder": 2,
    "TMEM165-congenital_disorder_of_glycosylation|not_specified": 2,
    "TMEM165-congenital_disorder_of_glycosylation|not_specified|not_provided|Congenital_disorder_of_glycosylation": 1,
    "TMEM165-congenital_disorder_of_glycosylation|TMEM165-related_disorder": 1,
    "TMEM165-related_disorder|not_provided|Congenital_disorder_of_glycosylation|TMEM165-congenital_disorder_of_glycosylation": 1,
    "not_provided|CEP135-related_disorder|not_specified": 4,
    "not_provided|CEP135-related_disorder": 3,
    "Microcephaly_8|_primary|_autosomal_recessive": 18,
    "CEP135-related_disorder|not_specified|not_provided": 3,
    "CEP135-related_disorder|not_provided": 2,
    "CEP135-related_disorder": 5,
    "CEP135-related_disorder|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly_8|_primary|_autosomal_recessive": 1,
    "not_provided|Microcephaly_8|_primary|_autosomal_recessive|not_specified": 1,
    "not_provided|Microcephaly_8|_primary|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|Microcephaly_8|_primary|_autosomal_recessive|not_provided": 1,
    "Microcephaly_8|_primary|_autosomal_recessive|not_provided": 2,
    "not_specified|not_provided|CEP135-related_disorder": 3,
    "Inborn_genetic_diseases|CEP135-related_disorder": 1,
    "Inborn_genetic_diseases|Microcephaly_8|_primary|_autosomal_recessive": 1,
    "not_specified|not_provided|Microcephaly_8|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CEP135-related_disorder|not_specified|not_provided": 1,
    "Microcephaly_8|_primary|_autosomal_recessive|CEP135-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|CEP135-related_disorder|not_provided": 1,
    "not_provided|See_cases|not_specified": 3,
    "Phosphoribosylaminoimidazole_carboxylase_deficiency": 3,
    "Autosomal_dominant_aplasia_and_myelodysplasia|SRP72-related_disorder": 1,
    "Autosomal_dominant_aplasia_and_myelodysplasia|not_specified": 2,
    "Autosomal_dominant_aplasia_and_myelodysplasia": 41,
    "not_specified|SRP72-related_disorder": 4,
    "SRP72-related_disorder|Autosomal_dominant_aplasia_and_myelodysplasia|not_provided": 1,
    "Autosomal_dominant_aplasia_and_myelodysplasia|not_specified|not_provided|SRP72-related_disorder": 1,
    "not_provided|Autosomal_dominant_aplasia_and_myelodysplasia": 16,
    "not_specified|not_provided|Autosomal_dominant_aplasia_and_myelodysplasia": 5,
    "not_provided|not_specified|Autosomal_dominant_aplasia_and_myelodysplasia": 8,
    "SRP72-related_disorder|not_specified|not_provided": 1,
    "Autosomal_dominant_aplasia_and_myelodysplasia|not_provided": 8,
    "Autosomal_dominant_aplasia_and_myelodysplasia|not_specified|not_provided": 2,
    "not_provided|SRP72-related_disorder|not_specified": 2,
    "not_specified|Autosomal_dominant_aplasia_and_myelodysplasia|not_provided": 2,
    "not_provided|SRP72-related_disorder": 4,
    "not_provided|Autosomal_dominant_aplasia_and_myelodysplasia|not_specified": 2,
    "not_specified|not_provided|SRP72-related_disorder|Autosomal_dominant_aplasia_and_myelodysplasia": 1,
    "Autosomal_dominant_aplasia_and_myelodysplasia|not_provided|not_specified": 2,
    "not_provided|not_specified|Autosomal_dominant_aplasia_and_myelodysplasia|SRP72-related_disorder": 1,
    "not_specified|SRP72-related_disorder|not_provided": 2,
    "SRP72-related_disorder": 8,
    "SRP72-related_disorder|not_provided": 5,
    "not_provided|not_specified|SRP72-related_disorder|Autosomal_dominant_aplasia_and_myelodysplasia": 1,
    "Autosomal_dominant_aplasia_and_myelodysplasia|not_provided|SRP72-related_disorder": 1,
    "SRP72-related_disorder|not_provided|not_specified|Autosomal_dominant_aplasia_and_myelodysplasia": 1,
    "not_specified|not_provided|SRP72-related_disorder": 1,
    "SRP72-related_disorder|not_provided|not_specified": 6,
    "not_specified|not_provided|Autosomal_dominant_aplasia_and_myelodysplasia|SRP72-related_disorder": 2,
    "SRP72-related_disorder|Autosomal_dominant_aplasia_and_myelodysplasia|not_specified|not_provided": 1,
    "SRP72-related_disorder|not_specified": 1,
    "SPINK2-related_disorder": 6,
    "Spermatogenic_failure_29": 2,
    "REST-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "REST-related_disorder": 19,
    "REST-related_disorder|not_provided": 16,
    "Fibromatosis|_gingival|_5": 4,
    "not_provided|REST-related_disorder": 16,
    "Wilms_tumor_6|Autosomal_dominant_nonsyndromic_hearing_loss_27|Fibromatosis|_gingival|_5|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|REST-related_disorder": 1,
    "not_provided|Wilms_tumor_6": 4,
    "not_provided|Wilms_tumor_6|Fibromatosis|_gingival|_5|Autosomal_dominant_nonsyndromic_hearing_loss_27|Inborn_genetic_diseases": 1,
    "Wilms_tumor_6": 9,
    "Autosomal_dominant_nonsyndromic_hearing_loss_27|Fibromatosis|_gingival|_5|Wilms_tumor_6": 18,
    "Fibromatosis|_gingival|_5|Wilms_tumor_6|Autosomal_dominant_nonsyndromic_hearing_loss_27|not_provided|Inborn_genetic_diseases": 1,
    "Fibromatosis|_gingival|_5|Autosomal_dominant_nonsyndromic_hearing_loss_27|Wilms_tumor_6|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Fibromatosis|_gingival|_5|Autosomal_dominant_nonsyndromic_hearing_loss_27|Wilms_tumor_6": 4,
    "not_provided|Fibromatosis|_gingival|_5|Wilms_tumor_6|Autosomal_dominant_nonsyndromic_hearing_loss_27": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_27": 1,
    "Childhood_kidney_Wilms_tumor": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_27|Autosomal_dominant_nonsyndromic_hearing_loss": 1,
    "Fibromatosis|_gingival|_1|Fibromatosis|_gingival|_5": 2,
    "Inborn_genetic_diseases|Wilms_tumor_6|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|REST-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|REST-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_27|Fibromatosis|_gingival|_5|Wilms_tumor_6|not_provided": 2,
    "REST-related_disorder|Wilms_tumor_6|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_27|Wilms_tumor_6|Fibromatosis|_gingival|_5|not_provided": 1,
    "Fibromatosis|_gingival|_5|Autosomal_dominant_nonsyndromic_hearing_loss_27|Wilms_tumor_6|not_provided": 3,
    "not_provided|REST-related_disorder|not_specified": 1,
    "Wilms_tumor_6|Autosomal_dominant_nonsyndromic_hearing_loss_27|Fibromatosis|_gingival|_5|REST-related_disorder|not_provided": 1,
    "REST-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_27|Wilms_tumor_6|Fibromatosis|_gingival|_5": 2,
    "Fibromatosis|_gingival|_5|Inborn_genetic_diseases": 1,
    "Fibromatosis|_gingival|_5|Wilms_tumor_6|Autosomal_dominant_nonsyndromic_hearing_loss_27|not_provided": 2,
    "Wilms_tumor_6|Fibromatosis|_gingival|_5|Autosomal_dominant_nonsyndromic_hearing_loss_27|not_provided": 1,
    "not_provided|Fibromatosis|_gingival|_1|Fibromatosis|_gingival|_5": 1,
    "not_provided|REST-related_disorder|Fibromatosis|_gingival|_5|Wilms_tumor_6|Autosomal_dominant_nonsyndromic_hearing_loss_27|Inborn_genetic_diseases": 1,
    "Wilms_tumor_6|Inborn_genetic_diseases|not_provided": 1,
    "Fibromatosis|_gingival|_5|Autosomal_dominant_nonsyndromic_hearing_loss_27|Wilms_tumor_6|not_provided|REST-related_disorder": 1,
    "Retinal_arterial_macroaneurysm_with_supravascular_pulmonic_stenosis|Familial_retinal_arterial_macroaneurysm|not_provided": 1,
    "Familial_retinal_arterial_macroaneurysm": 1,
    "not_provided|Familial_retinal_arterial_macroaneurysm": 1,
    "IGFBP7-related_disorder|Inborn_genetic_diseases": 1,
    "IGFBP7-related_disorder": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_3|Cardiovascular_phenotype": 4,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_3": 7,
    "Cardiovascular_phenotype|TECRL-related_disorder": 3,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_3|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_3": 1,
    "TECRL-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_3": 1,
    "Cardiovascular_phenotype|TECRL-related_disorder|not_specified|not_provided": 1,
    "TECRL-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "TECRL-related_disorder": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_3|TECRL-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|TECRL-related_disorder|not_provided": 1,
    "Astrocytoma": 4,
    "STAP1-related_disorder": 2,
    "STAP1-related_disorder|not_provided": 1,
    "not_provided|not_specified|STAP1-related_disorder": 1,
    "STAP1-related_disorder|not_specified": 1,
    "Isolated_GnRH_Deficiency": 16,
    "GNRHR-related_disorder|not_provided": 1,
    "Hypogonadotropic_hypogonadism|not_provided|See_cases|Amenorrhea|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "GNRHR-related_disorder": 2,
    "not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_specified": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "GNRHR-related_disorder|not_specified|not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "GNRHR-related_disorder|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Isolated_GnRH_Deficiency|not_provided": 2,
    "Amenorrhea|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "not_provided|not_specified|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "not_provided|GNRHR-related_disorder|not_specified|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism|not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "not_provided|Isolated_congenital_hypogonadotropic_hypogonadism": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Delayed_puberty": 1,
    "Infertility_disorder|not_provided|GNRHR-related_disorder|Hypogonadotropic_hypogonadism|Inborn_genetic_diseases|Isolated_congenital_hypogonadotropic_hypogonadism|Gonadotropin_deficiency|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Isolated_GnRH_Deficiency|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Isolated_GnRH_Deficiency": 1,
    "YTHDC1-related_disorder": 1,
    "TMPRSS11E-related_disorder": 1,
    "UGT2B17-related_disorder": 8,
    "not_provided|UGT2B17-related_disorder": 4,
    "Tramadol_response": 1572,
    "Tramadol_response|not_provided": 9,
    "not_provided|Tramadol_response": 4,
    "Asthma|_protection_against|not_provided": 1,
    "AMTN-related_disorder": 5,
    "Amelogenesis_imperfecta_type_3B": 1,
    "Amelogenesis_imperfecta|_type_3A": 9,
    "not_provided|AMTN-related_disorder": 1,
    "Amelogenesis_imperfecta_type_1F": 9,
    "not_provided|Amelogenesis_imperfecta_type_1F": 1,
    "AMBN-related_disorder": 8,
    "Amelogenesis_imperfecta_type_1F|not_specified": 1,
    "not_provided|AMBN-related_disorder": 3,
    "Amelogenesis_imperfecta_type_1F|not_provided": 1,
    "Amelogenesis_imperfecta_type_1F|AMBN-related_disorder|not_provided": 1,
    "AMBN-related_disorder|not_provided": 1,
    "Amelogenesis_imperfecta|not_provided": 14,
    "Amelogenesis_imperfecta_-_hypoplastic_autosomal_dominant_-_local": 9,
    "ENAM-related_disorder": 5,
    "not_provided|Amelogenesis_imperfecta": 9,
    "Amelogenesis_imperfecta_type_1C|Amelogenesis_imperfecta_-_hypoplastic_autosomal_dominant_-_local": 2,
    "not_provided|Amelogenesis_imperfecta_-_hypoplastic_autosomal_dominant_-_local": 2,
    "not_provided|Amelogenesis_imperfecta_-_hypoplastic_autosomal_dominant_-_local|ENAM-related_disorder": 1,
    "not_provided|Amelogenesis_imperfecta|ENAM-related_disorder": 1,
    "ENAM-related_disorder|Amelogenesis_imperfecta_-_hypoplastic_autosomal_dominant_-_local|Amelogenesis_imperfecta_type_1C|Inborn_genetic_diseases|not_provided": 1,
    "Amelogenesis_imperfecta_type_1C": 1,
    "Amelogenesis_imperfecta|not_provided|ENAM-related_disorder": 1,
    "not_specified|Amelogenesis_imperfecta|not_provided": 2,
    "Amelogenesis_imperfecta|Inborn_genetic_diseases": 2,
    "Amelogenesis_imperfecta_type_1C|Amelogenesis_imperfecta_-_hypoplastic_autosomal_dominant_-_local|not_provided": 1,
    "Amelogenesis_Imperfecta|_Dominant": 6,
    "SLC4A4-related_disorder": 4,
    "Autosomal_recessive_proximal_renal_tubular_acidosis": 176,
    "not_specified|not_provided|Autosomal_recessive_proximal_renal_tubular_acidosis": 1,
    "Autosomal_recessive_proximal_renal_tubular_acidosis|Inborn_genetic_diseases": 11,
    "not_provided|Autosomal_recessive_proximal_renal_tubular_acidosis": 23,
    "Inborn_genetic_diseases|Autosomal_recessive_proximal_renal_tubular_acidosis|not_provided": 4,
    "not_provided|Autosomal_recessive_proximal_renal_tubular_acidosis|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_proximal_renal_tubular_acidosis|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_recessive_proximal_renal_tubular_acidosis|not_provided": 24,
    "SLC4A4-related_disorder|Autosomal_recessive_proximal_renal_tubular_acidosis|not_provided": 2,
    "not_provided|SLC4A4-related_disorder": 3,
    "Combined_oxidative_phosphorylation_defect_type_24": 22,
    "Inborn_genetic_diseases|Autosomal_recessive_proximal_renal_tubular_acidosis": 4,
    "SLC4A4-related_disorder|not_provided|Autosomal_recessive_proximal_renal_tubular_acidosis": 4,
    "Autosomal_recessive_proximal_renal_tubular_acidosis|SLC4A4-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_proximal_renal_tubular_acidosis": 1,
    "SLC4A4-related_disorder|Autosomal_recessive_proximal_renal_tubular_acidosis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_proximal_renal_tubular_acidosis|not_specified": 1,
    "Chronic_obstructive_pulmonary_disease": 25,
    "Chronic_obstructive_pulmonary_disease|not_provided": 2,
    "Levothyroxine_response|not_provided|GC1/GC2_POLYMORPHISM": 1,
    "Periodontitis|not_provided|GC1/GC2_POLYMORPHISM": 1,
    "ADAMTS3-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|ADAMTS3-related_disorder|not_provided": 1,
    "not_provided|ADAMTS3-related_disorder": 3,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_3": 8,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_3|Inborn_genetic_diseases": 2,
    "not_specified|ADAMTS3-related_disorder|not_provided": 1,
    "ADAMTS3-related_disorder": 14,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_3|not_provided": 1,
    "not_provided|ADAMTS3-related_disorder|Hennekam_lymphangiectasia-lymphedema_syndrome_3": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_3|not_provided|ADAMTS3-related_disorder": 1,
    "Chopra-Amiel-Gordon_syndrome": 63,
    "ANKRD17-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Chopra-Amiel-Gordon_syndrome": 3,
    "ANKRD17-related_disorder": 26,
    "Chopra-Amiel-Gordon_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "ANKRD17-related_disorder|See_cases": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Chopra-Amiel-Gordon_syndrome": 1,
    "Intellectual_disability|Chopra-Amiel-Gordon_syndrome": 1,
    "Chopra-Amiel-Gordon_syndrome|not_provided": 3,
    "not_provided|ANKRD17-related_disorder": 2,
    "not_provided|Chopra-Amiel-Gordon_syndrome": 2,
    "ANKRD17-related_disorder|Chopra-Amiel-Gordon_syndrome": 1,
    "Inborn_genetic_diseases|ANKRD17-related_disorder": 2,
    "Hyperthyroxinemia|_dysalbuminemic": 1,
    "Hyperthyroxinemia|_familial_dysalbuminemic": 27,
    "Hyperthyroxinemia|_familial_dysalbuminemic|PROALBUMIN_MALMO": 1,
    "PROALBUMIN_LILLE": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type": 6,
    "Alloalbuminemia": 11,
    "PROALBUMIN_JAFFNA": 1,
    "ALBUMIN_LARINO": 1,
    "Analbuminemia_Baghdad": 1,
    "ALBUMIN_NAGASAKI_3": 1,
    "Hyperthyroxinemia|_familial_dysalbuminemic|not_provided": 16,
    "Analbuminemia": 10,
    "Analbuminemia|not_provided": 2,
    "Hyperthyroxinemia|_familial_dysalbuminemic|Inborn_genetic_diseases": 1,
    "ALBUMIN_TORINO": 1,
    "ALBUMIN_MALMO-95": 1,
    "not_provided|Hyperthyroxinemia|_familial_dysalbuminemic": 5,
    "ALBUMIN_VIBO_VALENTIA": 1,
    "ALBUMIN_YANOMAMA_2": 1,
    "ALBUMIN_NAGOYA": 1,
    "ALBUMIN_KOMAGOME_2": 1,
    "ALBUMIN_ASOLA": 1,
    "ALBUMIN_HAWKES_BAY": 1,
    "ALB-related_disorder": 2,
    "not_provided|Analbuminemia": 2,
    "not_specified|Hyperthyroxinemia|_familial_dysalbuminemic|ALB-related_disorder|not_provided": 1,
    "Hyperthyroxinemia|_familial_dysalbuminemic|ALBUMIN_TRADATE_2": 1,
    "ALBUMIN_HERBORN": 1,
    "ALBUMIN_MALMO-10": 1,
    "ALBUMIN_CASERTA": 1,
    "Hyperthyroxinemia|_familial_dysalbuminemic|ALBUMIN_TAGLIACOZZO": 1,
    "ALBUMIN_MALMO-47": 1,
    "ALBUMIN_ROMA": 1,
    "ALB-related_disorder|not_provided": 1,
    "ALBUMIN_SONDRIA": 1,
    "ALBUMIN_HIROSHIMA_1": 1,
    "ALBUMIN_COARI_I": 1,
    "ALBUMIN_PARKLANDS": 1,
    "Hyperthyroxinemia|_familial_dysalbuminemic|ALBUMIN_IOWA_CITY_1": 1,
    "ALBUMIN_NASKAPI": 1,
    "not_provided|ALBUMIN_NAGASAKI_2": 1,
    "ALBUMIN_TOCHIGI": 1,
    "ALBUMIN_MALMO-5": 1,
    "ALBUMIN_HIROSHIMA_2": 1,
    "Inborn_genetic_diseases|Hyperthyroxinemia|_familial_dysalbuminemic": 1,
    "ALBUMIN_DUBLIN": 1,
    "Hyperthyroxinemia|_familial_dysalbuminemic|ALBUMIN_CASEBROOK": 1,
    "not_provided|ALBUMIN_VANCOUVER": 1,
    "ALBUMIN_ORTONOVO": 1,
    "not_provided|Analbuminemia|Alloalbuminemia": 1,
    "ALBUMIN_CASTEL_DI_SANGRO": 1,
    "ALBUMIN_MEXICO_2|not_provided": 1,
    "ALBUMIN_FUKUOKA_1": 1,
    "ALBUMIN_OSAKA_1": 1,
    "ALBUMIN_BAZZANO": 1,
    "ALBUMIN_B": 1,
    "ALBUMIN_RUGBY_PARK": 1,
    "ALBUMIN_VANVES": 1,
    "ALBUMIN_VENEZIA": 1,
    "Alpha-fetoprotein|_hereditary_persistence_of": 7,
    "AFP-related_disorder": 5,
    "Alpha-fetoprotein_deficiency": 3,
    "CXCL8-related_disorder": 1,
    "ODAPH-related_disorder|Amelogenesis_imperfecta_hypomaturation_type_2A4": 2,
    "ODAPH-related_disorder": 5,
    "Amelogenesis_imperfecta_hypomaturation_type_2A4": 2,
    "not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A4": 1,
    "CDKL2-related_condition": 1,
    "USO1-related_disorder": 1,
    "Dystonia_37|_early-onset|_with_striatal_lesions": 5,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 34,
    "Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy": 9,
    "not_provided|Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy": 4,
    "Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 26,
    "Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_provided": 9,
    "not_provided|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Action_myoclonus-renal_failure_syndrome": 3,
    "Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|not_provided": 1,
    "Action_myoclonus-renal_failure_syndrome|not_provided|Progressive_myoclonic_epilepsy": 2,
    "not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome": 2,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome": 2,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome|not_provided": 1,
    "Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome": 14,
    "not_specified|Progressive_myoclonic_epilepsy": 10,
    "Progressive_myoclonic_epilepsy|not_specified|not_provided|Action_myoclonus-renal_failure_syndrome": 1,
    "not_provided|SCARB2-related_disorder|Action_myoclonus-renal_failure_syndrome|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 1,
    "not_provided|Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|not_specified": 1,
    "not_specified|Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "Action_myoclonus-renal_failure_syndrome|not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|Action_myoclonus-renal_failure_syndrome": 1,
    "not_provided|not_specified|Progressive_myoclonic_epilepsy": 3,
    "Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|not_specified": 2,
    "Action_myoclonus-renal_failure_syndrome|SCARB2-related_disorder|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Self-limited_epilepsy_with_centrotemporal_spikes|Action_myoclonus-renal_failure_syndrome": 1,
    "Action_myoclonus-renal_failure_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_myoclonic_epilepsy|not_provided|Inborn_genetic_diseases|Action_myoclonus-renal_failure_syndrome": 1,
    "Progressive_myoclonic_epilepsy|not_provided|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy": 1,
    "Action_myoclonus-renal_failure_syndrome|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 3,
    "Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 1,
    "Progressive_myoclonic_epilepsy|not_provided|Action_myoclonus-renal_failure_syndrome": 2,
    "Progressive_myoclonic_epilepsy|SCARB2-related_disorder|Inborn_genetic_diseases|not_provided|Action_myoclonus-renal_failure_syndrome": 1,
    "Action_myoclonus-renal_failure_syndrome|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Action_myoclonus-renal_failure_syndrome|not_specified|Progressive_myoclonic_epilepsy": 1,
    "SCARB2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome": 4,
    "Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome|not_provided": 2,
    "Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|SCARB2-related_disorder|not_provided|not_specified|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_specified|not_provided|Action_myoclonus-renal_failure_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "not_specified|Progressive_myoclonic_epilepsy|SCARB2-related_disorder": 1,
    "SCARB2-related_disorder|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_specified|not_provided|Action_myoclonus-renal_failure_syndrome": 1,
    "not_provided|Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 1,
    "SCARB2-related_disorder|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Progressive_myoclonic_epilepsy|SCARB2-related_disorder|Inborn_genetic_diseases|Action_myoclonus-renal_failure_syndrome": 1,
    "Action_myoclonus-renal_failure_syndrome|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Action_myoclonus-renal_failure_syndrome|SCARB2-related_disorder|Focal_segmental_glomerulosclerosis|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|not_specified": 1,
    "Progressive_myoclonic_epilepsy|SCARB2-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Action_myoclonus-renal_failure_syndrome|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|not_specified|Action_myoclonus-renal_failure_syndrome": 1,
    "Action_myoclonus-renal_failure_syndrome|SCARB2-related_disorder|Progressive_myoclonic_epilepsy|not_provided": 1,
    "SCARB2-related_disorder|Progressive_myoclonic_epilepsy": 1,
    "Action_myoclonus-renal_failure_syndrome|not_specified|SCARB2-related_disorder|not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 1,
    "Action_myoclonus-renal_failure_syndrome|not_provided": 1,
    "Action_myoclonus-renal_failure_syndrome|SCARB2-related_disorder|Progressive_myoclonic_epilepsy": 1,
    "Progressive_myoclonic_epilepsy|not_specified|SCARB2-related_disorder": 1,
    "not_specified|Progressive_myoclonic_epilepsy|Action_myoclonus-renal_failure_syndrome": 1,
    "not_provided|Action_myoclonus-renal_failure_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_specified|Action_myoclonus-renal_failure_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Self-limited_epilepsy_with_centrotemporal_spikes|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_specified|not_provided": 2,
    "not_specified|Progressive_myoclonic_epilepsy|not_provided|Action_myoclonus-renal_failure_syndrome": 1,
    "not_specified|Progressive_myoclonic_epilepsy|not_provided": 1,
    "SHROOM3-related_disorder": 24,
    "not_specified|SHROOM3-related_disorder|not_provided": 1,
    "SHROOM3-related_disorder|not_provided": 11,
    "not_provided|SHROOM3-related_disorder": 6,
    "SHROOM3-related_disorder|not_provided|not_specified": 4,
    "not_specified|SHROOM3-related_disorder": 1,
    "SHROOM3-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|SHROOM3-related_disorder": 1,
    "not_specified|not_provided|SHROOM3-related_disorder": 1,
    "Fraser_syndrome_1": 607,
    "not_provided|Fraser_syndrome_1": 168,
    "not_provided|FRAS1-related_disorder": 38,
    "Fraser_syndrome_1|not_provided": 123,
    "not_provided|not_specified|Fraser_syndrome_1": 18,
    "FRAS1-related_disorder|not_provided": 29,
    "not_specified|Fraser_syndrome_1|not_provided": 7,
    "FRAS1-related_disorder|not_provided|Fraser_syndrome_1": 20,
    "not_specified|not_provided|Fraser_syndrome_1": 20,
    "not_provided|FRAS1-related_disorder|Fraser_syndrome_1": 10,
    "Fraser_syndrome_1|Inborn_genetic_diseases|not_provided": 9,
    "Cryptophthalmos_syndrome|Fraser_syndrome_1": 2,
    "Fraser_syndrome_1|Inborn_genetic_diseases": 44,
    "Inborn_genetic_diseases|not_provided|Fraser_syndrome_1": 19,
    "FRAS1-related_disorder|Fraser_syndrome_1|not_provided": 8,
    "Inborn_genetic_diseases|Fraser_syndrome_1": 43,
    "FRAS1-related_disorder|Fraser_syndrome_1|Inborn_genetic_diseases": 2,
    "not_provided|Fraser_syndrome_1|not_specified": 7,
    "Fraser_syndrome_1|FRAS1-related_disorder|not_provided": 8,
    "Fraser_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2C|not_provided|Fraser_syndrome_1|not_specified": 1,
    "FRAS1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Fraser_syndrome_1|Inborn_genetic_diseases": 11,
    "Fraser_syndrome_1|not_specified": 3,
    "Fraser_syndrome_1|not_provided|Inborn_genetic_diseases": 13,
    "FRAS1-related_disorder": 26,
    "not_provided|Fraser_syndrome_1|FRAS1-related_disorder": 8,
    "Fraser_syndrome_1|not_specified|not_provided|FRAS1-related_disorder": 1,
    "not_specified|Fraser_syndrome_1": 5,
    "not_provided|Congenital_anomaly_of_kidney_and_urinary_tract|Inborn_genetic_diseases": 1,
    "not_specified|Fraser_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fraser_syndrome_1|not_provided": 9,
    "not_provided|not_specified|FRAS1-related_disorder|Fraser_syndrome_1": 4,
    "Fraser_syndrome_1|not_provided|not_specified": 6,
    "not_provided|Inborn_genetic_diseases|FRAS1-related_disorder|not_specified": 1,
    "FRAS1-related_disorder|Fraser_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Fraser_syndrome_1|not_specified": 1,
    "Fraser_syndrome_1|FRAS1-related_disorder|Inborn_genetic_diseases": 1,
    "Fraser_syndrome_1|Congenital_diaphragmatic_hernia|FRAS1-related_disorder": 1,
    "not_provided|Fraser_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Fraser_syndrome_1|not_provided|FRAS1-related_disorder": 5,
    "Inborn_genetic_diseases|FRAS1-related_disorder|Fraser_syndrome_1|not_provided": 1,
    "Fraser_syndrome_1|not_specified|not_provided": 6,
    "FRAS1-related_disorder|not_specified": 1,
    "not_provided|Fraser_syndrome_1|FRAS1-related_disorder|Inborn_genetic_diseases": 1,
    "Rieger_anomaly|not_provided": 1,
    "FRAS1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|FRAS1-related_disorder": 1,
    "FRAS1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Fraser_syndrome_1": 1,
    "not_specified|Inborn_genetic_diseases|Fraser_syndrome_1|not_provided": 1,
    "Fraser_syndrome_1|Cryptophthalmos_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "FRAS1-related_disorder|not_specified|not_provided|Fraser_syndrome_1": 2,
    "Inborn_genetic_diseases|Fraser_syndrome_1|not_specified": 2,
    "not_provided|FRAS1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Fraser_syndrome_1": 6,
    "Inborn_genetic_diseases|not_specified|Fraser_syndrome_1": 1,
    "Inborn_genetic_diseases|FRAS1-related_disorder": 2,
    "Congenital_diaphragmatic_hernia|not_provided|Fraser_syndrome_1": 1,
    "Cryptophthalmos_syndrome": 1,
    "FRAS1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Fraser_syndrome_1|FRAS1-related_disorder": 1,
    "not_specified|not_provided|FRAS1-related_disorder|Fraser_syndrome_1": 1,
    "FRAS1-related_disorder|not_provided|not_specified|Fraser_syndrome_1": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|FRAS1-related_disorder|Fraser_syndrome_1": 1,
    "Fraser_syndrome_1|not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|not_specified": 1,
    "not_provided|Fraser_syndrome_1|not_specified|FRAS1-related_disorder": 1,
    "FRAS1-related_disorder|not_provided|Fraser_syndrome_1|Inborn_genetic_diseases|Microcephaly": 1,
    "Fraser_syndrome_1|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Inborn_genetic_diseases|FRAS1-related_disorder|not_provided|Fraser_syndrome_1": 2,
    "not_specified|not_provided|FRAS1-related_disorder|Fraser_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|FRAS1-related_disorder|not_specified": 1,
    "FRAS1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Anophthalmia-microphthalmia_syndrome|Fraser_syndrome_1": 1,
    "not_specified|Fraser_syndrome_1|FRAS1-related_disorder|not_provided": 1,
    "not_specified|FRAS1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Fraser_syndrome_1|Congenital_diaphragmatic_hernia": 1,
    "Fraser_syndrome_1|not_specified|FRAS1-related_disorder": 1,
    "Fraser_syndrome_1|Cryptophthalmos_syndrome": 1,
    "FRAS1-related_disorder|Inborn_genetic_diseases|not_provided|Fraser_syndrome_1": 1,
    "not_specified|not_provided|FRAS1-related_disorder": 1,
    "FRAS1-related_disorder|Fraser_syndrome_1|not_specified|not_provided": 1,
    "not_provided|FRAS1-related_disorder|Fraser_syndrome_1|not_specified": 1,
    "Hyaline_fibromatosis_syndrome": 145,
    "not_provided|Hyaline_fibromatosis_syndrome": 12,
    "Hyaline_fibromatosis_syndrome|not_provided": 17,
    "Inborn_genetic_diseases|Hyaline_fibromatosis_syndrome": 2,
    "ANTXR2-related_disorder|Hyaline_fibromatosis_syndrome|not_provided": 4,
    "ANTXR2-related_disorder|not_provided": 2,
    "not_specified|Hyaline_fibromatosis_syndrome": 1,
    "not_provided|not_specified|Hyaline_fibromatosis_syndrome": 1,
    "ANTXR2-related_disorder": 4,
    "not_provided|ANTXR2-related_disorder": 1,
    "Hyaline_fibromatosis_syndrome|not_provided|ANTXR2-related_disorder": 1,
    "Hyaline_fibromatosis_syndrome|not_specified|not_provided": 1,
    "Hyaline_fibromatosis_syndrome|Juvenile_hyaline_fibromatosis": 1,
    "Hyaline_fibromatosis_syndrome|Inborn_genetic_diseases": 1,
    "Hyaline_fibromatosis_syndrome|not_provided|Central_core_myopathy": 1,
    "Early-onset_Lafora_body_disease": 367,
    "Early-onset_Lafora_body_disease|not_specified": 22,
    "not_specified|Early-onset_Lafora_body_disease": 19,
    "not_provided|Early-onset_Lafora_body_disease": 5,
    "not_provided|not_specified|Early-onset_Lafora_body_disease": 2,
    "Early-onset_Lafora_body_disease|PRDM8-related_disorder": 1,
    "PRDM8-related_disorder|Early-onset_Lafora_body_disease": 4,
    "Early-onset_Lafora_body_disease|not_provided": 6,
    "not_provided|PRDM8-related_disorder|Early-onset_Lafora_body_disease": 1,
    "Early-onset_Lafora_body_disease|PRDM8-related_disorder|not_provided": 1,
    "PRDM8-related_disorder|Early-onset_Lafora_body_disease|not_provided": 1,
    "Early-onset_Lafora_body_disease|not_specified|not_provided": 1,
    "FGF5-related_disorder": 3,
    "Trichomegaly": 3,
    "not_provided|FGF5-related_disorder": 1,
    "Spondylometaphyseal_dysplasia|_pagnamenta_type": 1,
    "not_provided|PRKG2-related_disorder": 1,
    "PRKG2-related_disorder": 10,
    "Acromesomelic_dysplasia_4": 7,
    "RASGEF1B-related_disorder": 4,
    "not_provided|RASGEF1B-related_disorder": 1,
    "HNRNPD-related_disorder": 2,
    "HNRNPD-related_disorder|not_specified": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G": 347,
    "not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G": 11,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G|not_provided": 8,
    "HNRNPDL-related_myopathy_with_protein_aggregates_and_rimmed_vacuoles|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G": 1,
    "not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G": 20,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G|not_specified": 20,
    "HNRNPDL-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G": 4,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G|HNRNPDL-related_disorder": 2,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G|not_provided|not_specified": 1,
    "HNRNPDL-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1G|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_79": 2,
    "not_specified|Hearing_loss|_autosomal_dominant_79": 1,
    "Neurodevelopmental_disorder_with_spastic_quadriplegia|_optic_atrophy|_seizures|_and_structural_brain_anomalies": 2,
    "SEC31A-related_disorder": 2,
    "Neurodevelopmental_disorder_with_spastic_quadriplegia|_optic_atrophy|_seizures|_and_structural_brain_anomalies|not_provided": 6,
    "Neurodevelopmental_disorder_with_spastic_quadriplegia|_optic_atrophy|_seizures|_and_structural_brain_anomalies|Kaya-Barakat-Masson_syndrome": 1,
    "SEC31A-related_disorder|not_provided": 1,
    "Coenzyme_Q10_deficiency": 10,
    "COQ2-related_disorder": 8,
    "COQ2-related_disorder|not_provided": 8,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_provided": 7,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to": 31,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_1|Coenzyme_Q10_deficiency|Multiple_system_atrophy_1|_susceptibility_to": 1,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|COQ2-related_disorder|not_provided": 1,
    "Multiple_system_atrophy|not_provided": 1,
    "Coenzyme_Q10_deficiency|Multiple_system_atrophy": 1,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to": 8,
    "not_provided|COQ2-related_disorder": 2,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_provided|not_specified": 1,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|Inborn_genetic_diseases|not_provided": 3,
    "Coenzyme_Q10_deficiency|_primary|_1|not_provided|Multiple_system_atrophy_1|_susceptibility_to": 1,
    "Multiple_system_atrophy": 2,
    "Inborn_genetic_diseases|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to": 2,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|not_provided": 9,
    "not_provided|not_specified|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Inborn_genetic_diseases": 2,
    "not_provided|COQ2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1": 3,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "not_specified|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_provided": 1,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_specified|not_provided": 1,
    "not_specified|Coenzyme_Q10_deficiency|_primary|_1|not_provided": 1,
    "Coenzyme_Q10_deficiency|_primary|_1|not_provided": 3,
    "Coenzyme_Q10_deficiency|not_provided|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "Inborn_genetic_diseases|not_provided|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to": 1,
    "Nephrotic_syndrome|Coenzyme_Q10_deficiency|Inborn_genetic_diseases|not_provided|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "Multiple_system_atrophy_1|_susceptibility_to": 2,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|not_provided": 1,
    "Coenzyme_Q10_deficiency|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|not_provided|Inborn_genetic_diseases": 2,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency": 1,
    "not_provided|Neonatal_encephalopathy": 1,
    "Inborn_genetic_diseases|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|Multiple_system_atrophy|not_provided": 1,
    "not_provided|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "Focal_segmental_glomerulosclerosis|not_specified|not_provided": 1,
    "COQ2-related_disorder|not_provided|not_specified|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "not_specified|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Multiple_system_atrophy|not_provided": 1,
    "not_specified|COQ2-related_disorder|not_provided": 1,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_specified|COQ2-related_disorder|Mitochondrial_disease|not_provided": 1,
    "Inborn_genetic_diseases|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|COQ2-related_disorder": 1,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_1|not_specified": 1,
    "not_provided|Nephrotic_syndrome": 5,
    "Inborn_genetic_diseases|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_provided": 1,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Inborn_genetic_diseases": 2,
    "Coenzyme_Q10_deficiency|_primary|_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|COQ2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Coenzyme_Q10_deficiency|_primary|_1": 1,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_disease|Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|Inborn_genetic_diseases|not_provided": 1,
    "Multiple_system_atrophy_1|_susceptibility_to|Coenzyme_Q10_deficiency|_primary|_1|not_specified|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|not_provided|Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|Focal_segmental_glomerulosclerosis": 1,
    "Coenzyme_Q10_deficiency|_primary|_1|Multiple_system_atrophy_1|_susceptibility_to|not_provided|not_specified": 1,
    "HPSE-related_disorder": 7,
    "HELQ-related_disorder": 28,
    "HELQ-related_disorder|not_provided": 2,
    "not_specified|HELQ-related_disorder": 1,
    "not_provided|HELQ-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|ABRAXAS1-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "ABRAXAS1-related_disorder|not_specified|not_provided": 6,
    "Hereditary_breast_cancer|_ABRAXAS1-related|not_provided|not_specified": 1,
    "ABRAXAS1-related_disorder|not_provided|not_specified": 1,
    "not_provided|ABRAXAS1-related_disorder": 1,
    "CDS1-related_disorder": 9,
    "CDS1-related_disorder|not_specified": 2,
    "Microcephaly_18|_primary|_autosomal_dominant|Inborn_genetic_diseases": 2,
    "not_provided|WDFY3-related_disorder": 9,
    "WDFY3-related_disorder": 39,
    "Inborn_genetic_diseases|Microcephaly_18|_primary|_autosomal_dominant": 5,
    "Microcephaly_18|_primary|_autosomal_dominant": 59,
    "Microcephaly_18|_primary|_autosomal_dominant|not_provided": 4,
    "Inborn_genetic_diseases|Microcephaly_18|_primary|_autosomal_dominant|not_provided": 1,
    "Macrocephaly-autism_syndrome": 20,
    "WDFY3-related_disorder|Microcephaly_18|_primary|_autosomal_dominant|not_provided": 1,
    "Neurodevelopmental_delay|not_specified": 1,
    "not_provided|not_specified|Neurodevelopmental_delay": 1,
    "WDFY3-related_disorder|not_provided": 6,
    "not_provided|Microcephaly_18|_primary|_autosomal_dominant": 3,
    "Microcephaly_18|_primary|_autosomal_dominant|WDFY3-related_disorder": 2,
    "WDFY3-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|WDFY3-related_disorder": 3,
    "Neurodevelopmental_delay|Microcephaly_18|_primary|_autosomal_dominant": 1,
    "Macrocephaly|Microcephaly_18|_primary|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Esophageal_atresia/tracheoesophageal_fistula|not_specified": 1,
    "Microcephaly_18|_primary|_autosomal_dominant|WDFY3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ARHGAP24-related_disorder": 9,
    "not_provided|ARHGAP24-related_disorder": 6,
    "ARHGAP24-related_disorder|not_provided": 8,
    "not_specified|Focal_segmental_glomerulosclerosis_1": 1,
    "not_specified|ARHGAP24-related_disorder": 1,
    "not_provided|ARHGAP24-related_disorder|not_specified": 1,
    "MAPK10-related_disorder": 5,
    "Epileptic_encephalopathy_with_cognitive_deficit": 1,
    "MAPK10-related_disorder|Epileptic_encephalopathy": 1,
    "not_provided|PTPN13-related_disorder": 1,
    "PTPN13-related_disorder": 11,
    "PTPN13-related_disorder|not_provided": 2,
    "PTPN13-related_disorder|not_specified": 1,
    "not_specified|PTPN13-related_disorder": 2,
    "not_provided|HSD17B13_POLYMORPHISM|FATTY_LIVER_DISEASE|_PROTECTION_AGAINST": 1,
    "SPARCL1-related_disorder": 2,
    "SPARCL1-related_disorder|not_specified": 1,
    "Stromal_corneal_dystrophy": 1,
    "Denticles": 7,
    "not_provided|Dentinogenesis_imperfecta_type_2": 1,
    "Deafness|_autosomal_dominant_nonsyndromic_sensorineural_39|_with_dentinogenesis_imperfecta_1": 1,
    "DSPP-related_disorder": 7,
    "Dentinogenesis_imperfecta": 4,
    "Dentinogenesis_imperfecta_type_2|Deafness|_autosomal_dominant_nonsyndromic_sensorineural_39|_with_dentinogenesis_imperfecta_1|Dentinogenesis_imperfecta_type_3": 1,
    "Dentinogenesis_imperfecta_type_2": 17,
    "DSPP-related_disorder|not_provided": 2,
    "DSPP-related_disorder|not_provided|Dentinogenesis_imperfecta_type_2": 1,
    "not_specified|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|Denticles|Dentinogenesis_imperfecta_type_2|Dentinogenesis_imperfecta_type_3|not_provided": 2,
    "Dentinogenesis_imperfecta_type_2|Inborn_genetic_diseases": 1,
    "DSPP-related_disorder|not_provided|not_specified|Dentinogenesis_imperfecta_type_2|Dentinogenesis_imperfecta": 1,
    "not_provided|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1": 1,
    "not_provided|Dentinogenesis_imperfecta": 1,
    "not_provided|DSPP-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|DSPP-related_disorder": 1,
    "Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|Dentinogenesis_imperfecta_type_2|Denticles|Dentinogenesis_imperfecta_type_3|not_provided": 1,
    "DSPP-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|Inborn_genetic_diseases": 1,
    "Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1": 3,
    "Inborn_genetic_diseases|DSPP-related_disorder": 1,
    "Dentinogenesis_imperfecta_type_3": 2,
    "not_provided|Inborn_genetic_diseases|Dentinogenesis_imperfecta_type_2|Denticles|Dentinogenesis_imperfecta_type_3|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|DSPP-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss|Hereditary_optic_neuropathy": 1,
    "Hearing_impairment|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|not_specified": 1,
    "Denticles|Dentinogenesis_imperfecta_type_2|Dentinogenesis_imperfecta_type_3|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1": 1,
    "Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|Dentinogenesis_imperfecta_type_2|Denticles|Dentinogenesis_imperfecta_type_3": 1,
    "not_provided|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|not_specified": 1,
    "not_specified|Deafness|_autosomal_dominant_39|_with_dentinogenesis_imperfecta_1|Dentinogenesis_imperfecta_type_3|Denticles|not_provided|Dentinogenesis_imperfecta_type_2": 1,
    "Hypophosphatemic_Rickets|_Recessive": 4,
    "not_specified|not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_1": 4,
    "Hypophosphatemic_rickets": 14,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1": 60,
    "not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_1": 14,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|not_provided": 23,
    "not_provided|DMP1-related_disorder": 2,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|not_provided|not_specified": 1,
    "DMP1-related_disorder|not_provided": 2,
    "not_provided|not_specified|Hypophosphatemic_rickets|_autosomal_recessive|_1": 1,
    "not_specified|Hypophosphatemic_rickets|_autosomal_recessive|_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hypophosphatemic_rickets|_autosomal_recessive|_1": 4,
    "DMP1-related_disorder": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|not_specified": 1,
    "DMP1-related_disorder|not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_1": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_1": 1,
    "not_specified|Hypophosphatemic_rickets|_autosomal_recessive|_1|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Hypophosphatemic_rickets|_autosomal_recessive|_1": 1,
    "not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_1|not_specified": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|not_provided|Inborn_genetic_diseases": 2,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|Inborn_genetic_diseases": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_1|DMP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_1": 1,
    "MEPE-related_disorder": 17,
    "not_specified|MEPE-related_disorder": 3,
    "MEPE-related_disorder|not_specified": 2,
    "MEPE-related_disorder|not_provided": 4,
    "not_provided|MEPE-related_disorder": 2,
    "Polycystic_kidney_disease_2": 370,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 2,
    "PKD2-related_disorder": 25,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease": 17,
    "Polycystic_kidney_disease_2|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 14,
    "Polycystic_kidney_disease_2|PKD2-related_disorder": 2,
    "PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 5,
    "Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases": 16,
    "Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases|PKD2-related_disorder|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 34,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 43,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_2|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Polycystic_kidney_disease": 6,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease": 2,
    "Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_2": 4,
    "PKD2-related_disorder|Polycystic_kidney_disease_2|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease": 2,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases|PKD2-related_disorder": 1,
    "not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease_2": 1,
    "Polycystic_kidney_disease_2|Inborn_genetic_diseases": 9,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2|PKD2-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 4,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided": 29,
    "not_provided|Polycystic_kidney_disease_2": 23,
    "PKD2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 1,
    "PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease_2": 1,
    "Polycystic_kidney_disease_2|not_provided": 22,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 5,
    "Polycystic_kidney_disease_2|Polycystic_kidney_disease|Hypertensive_disorder|Chronic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|PKD2-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_2": 1,
    "PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|Polycystic_kidney_disease|not_specified|not_provided": 1,
    "Polycystic_kidney_disease_2|not_provided|Polycystic_kidney_disease": 2,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|Polycystic_kidney_disease_2": 2,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|Polycystic_kidney_disease_2|not_specified|not_provided": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_provided": 6,
    "not_specified|Polycystic_kidney_disease_2": 4,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 2,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|not_provided": 6,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease_2": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease_2|not_provided": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 4,
    "not_provided|not_specified|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease_2|not_provided|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|not_provided|PKD2-related_disorder": 3,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease": 3,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_provided|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2": 15,
    "Renal_cyst": 24,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 5,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Polycystic_kidney_disease|not_provided": 2,
    "PKD2-related_disorder|Polycystic_kidney_disease_2": 2,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|not_specified|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Polycystic_kidney_disease|Elevated_systolic_blood_pressure|Elevated_diastolic_blood_pressure": 1,
    "PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 1,
    "not_provided|PKD2-related_disorder|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type": 2501,
    "Multiple_renal_cysts|Anhydramnios|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease|PKD2-related_disorder": 1,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2|PKD2-related_disorder|Polycystic_kidney_disease": 1,
    "PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 2,
    "PKD2-related_disorder|Polycystic_kidney_disease_2|not_provided": 1,
    "Polycystic_kidney_disease_2|not_provided|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|PKD2-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease_2": 1,
    "Polycystic_kidney_disease_2|PKD2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|PKD2-related_disorder|not_provided|Polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "PKD2-related_disorder|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease|Renal_cyst": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease_2": 2,
    "Polycystic_kidney_disease_2|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 2,
    "Autosomal_dominant_polycystic_liver_disease|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Biliary_tract_abnormality|not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|not_provided|Autosomal_dominant_polycystic_kidney_disease": 4,
    "Polycystic_kidney_disease_2|not_provided|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 1,
    "PKD2-related_disorder|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2": 1,
    "not_provided|Polycystic_kidney_disease_2|Renal_cyst": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_provided": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_specified": 1,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease_2|not_specified|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|PKD2-related_disorder": 2,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|not_specified": 1,
    "not_provided|PKD2-related_disorder": 1,
    "Polycystic_kidney_disease|not_provided": 7,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|Kidney_failure": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_2|not_provided": 2,
    "not_specified|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|PKD2-related_disorder": 1,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|not_specified": 1,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder": 2,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_provided|PKD2-related_disorder": 1,
    "Anhydramnios|Enlarged_kidney|Hyperechogenic_kidneys|Multiple_renal_cysts|not_provided": 1,
    "Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_provided|Polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2": 1,
    "Polycystic_kidney_disease_2|not_specified": 1,
    "Polycystic_kidney_disease_2|not_provided|PKD2-related_disorder|not_specified": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|PKD2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder": 5,
    "Multiple_renal_cysts|Hydrocele_testis|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Multicystic_kidney_dysplasia|Polycystic_liver_disease_1|Polycystic_kidney_disease_2": 1,
    "not_specified|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases": 2,
    "PKD2-related_disorder|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|Polycystic_kidney_disease|PKD2-related_disorder": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease_2|Joubert_syndrome_7|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|Polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease_2|PKD2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Polycystic_kidney_disease_2|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|Polycystic_kidney_disease_2|not_specified": 1,
    "PKD2-related_disorder|not_provided|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_2|not_provided|Polycystic_kidney_disease|PKD2-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease_2|PKD2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|Polycystic_kidney_disease_2": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_2|not_specified": 1,
    "Autosomal_dominant_polycystic_kidney_disease|PKD2-related_disorder|Polycystic_kidney_disease_2|Polycystic_kidney_disease": 1,
    "PKD2-related_disorder|not_provided|Autosomal_dominant_polycystic_kidney_disease": 1,
    "ABCG2-related_disorder": 4,
    "BLOOD_GROUP|_JUNIOR_SYSTEM": 3,
    "BLOOD_GROUP|_JUNIOR_SYSTEM|URIC_ACID_CONCENTRATION|_SERUM|_QUANTITATIVE_TRAIT_LOCUS_1|not_specified|not_provided": 1,
    "ABCG2-related_disorder|BLOOD_GROUP|_JUNIOR_SYSTEM|URIC_ACID_CONCENTRATION|_SERUM|_QUANTITATIVE_TRAIT_LOCUS_1|Gemcitabine_response|rosuvastatin_response_-_Efficacy|rosuvastatin_response_-_Metabolism/PK": 1,
    "BLOOD_GROUP|_JUNIOR_SYSTEM|URIC_ACID_CONCENTRATION|_SERUM|_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "ABCG2-related_disorder|BLOOD_GROUP|_JUNIOR_SYSTEM|URIC_ACID_CONCENTRATION|_SERUM|_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "Maple_syrup_urine_disease|_mild_variant": 74,
    "Maple_syrup_urine_disease|_mild_variant|not_specified": 8,
    "not_specified|Maple_syrup_urine_disease|_mild_variant": 8,
    "not_provided|Maple_syrup_urine_disease|_mild_variant|PPM1K-related_disorder": 1,
    "PPM1K-related_disorder": 3,
    "Maple_syrup_urine_disease|_mild_variant|not_provided": 3,
    "not_specified|Maple_syrup_urine_disease|_mild_variant|not_provided": 1,
    "Maple_syrup_urine_disease|_mild_variant|PPM1K-related_disorder": 1,
    "PPM1K-related_disorder|not_provided": 1,
    "Maple_syrup_urine_disease|_mild_variant|PPM1K-related_disorder|not_provided": 1,
    "PPM1K-related_disorder|Maple_syrup_urine_disease|_mild_variant": 1,
    "not_specified|not_provided|Maple_syrup_urine_disease|_mild_variant": 1,
    "not_provided|Maple_syrup_urine_disease|_mild_variant": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_6|not_provided": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_6": 4,
    "not_specified|Squamous_cell_carcinoma": 1,
    "Interstitial_lung_disease_2|Combined_pulmonary_fibrosis-emphysema_syndrome|Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Chronic_obstructive_pulmonary_disease": 1,
    "FAM13A-related_pulmonary_fibrosis": 1,
    "Parkinson_Disease|_Dominant": 83,
    "Parkinson_Disease|_Dominant|not_provided": 11,
    "not_provided|Parkinson_Disease|_Dominant": 4,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Parkinson_Disease|_Dominant|not_provided": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1": 29,
    "Parkinson_Disease|_Dominant|Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Autosomal_dominant_Parkinson_disease_4|not_provided": 1,
    "Parkinson_Disease|_Dominant|Autosomal_dominant_Parkinson_disease_4|Autosomal_dominant_Parkinson_disease_1|Lewy_body_dementia|not_provided": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_4|Autosomal_dominant_Parkinson_disease_1|Parkinson_Disease|_Dominant|not_provided": 1,
    "Autosomal_dominant_Parkinson_disease_1|Lewy_body_dementia": 10,
    "Autosomal_dominant_Parkinson_disease_1": 4,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Autosomal_dominant_Parkinson_disease_4": 3,
    "Autosomal_dominant_Parkinson_disease_1|Lewy_body_dementia|Parkinson_Disease|_Dominant": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Parkinson_Disease|_Dominant": 1,
    "not_provided|Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Parkinson_Disease|_Dominant|SNCA-related_disorder": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Parkinson_Disease|_Dominant|Autosomal_dominant_Parkinson_disease_4": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|not_provided": 1,
    "not_provided|Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Parkinson_Disease|_Dominant": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Autosomal_dominant_Parkinson_disease_4|not_provided": 2,
    "Autosomal_dominant_Parkinson_disease_1|Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_4|not_provided": 1,
    "Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1|Autosomal_dominant_Parkinson_disease_4|Parkinson_Disease|_Dominant": 1,
    "SNCA-related_disorder|Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1": 1,
    "Autosomal_dominant_Parkinson_disease_4|Autosomal_dominant_Parkinson_disease_1|Lewy_body_dementia": 1,
    "Autosomal_dominant_Parkinson_disease_1|not_provided": 1,
    "not_provided|Lewy_body_dementia|Autosomal_dominant_Parkinson_disease_1": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_18": 12,
    "GRID2-related_disorder": 2,
    "not_provided|GRID2-related_disorder": 1,
    "GRID2-related_disorder|not_provided": 6,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_18": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_18": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_18|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_18|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|GRID2-related_disorder": 1,
    "GRID2-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_18|not_provided": 1,
    "ATOH1-related_disorder": 7,
    "Hearing_loss|_autosomal_dominant_89": 1,
    "not_specified|ATOH1-related_disorder": 1,
    "ATOH1-related_disorder|not_provided": 2,
    "Global_developmental_delay|Hearing_loss|Pontoneocerebellar_hypoplasia|See_cases": 1,
    "not_provided|ATOH1-related_disorder": 2,
    "Hearing_loss|_autosomal_dominant_89|Dominant_progressive_sensorineural_hearing_loss": 1,
    "Oculocutaneous_albinism_type_8": 9,
    "SMARCAD1-related_disorder": 4,
    "Keratoderma_with_scleroatrophy_of_the_extremities|Adermatoglyphia|not_provided|Basan_syndrome": 1,
    "Basan_syndrome|not_provided|Keratoderma_with_scleroatrophy_of_the_extremities|Adermatoglyphia": 2,
    "not_provided|SMARCAD1-related_disorder": 2,
    "Keratoderma_with_scleroatrophy_of_the_extremities": 1,
    "not_provided|Adermatoglyphia": 1,
    "not_provided|Keratoderma_with_scleroatrophy_of_the_extremities": 1,
    "Adermatoglyphia|Basan_syndrome": 1,
    "Adermatoglyphia|Keratoderma_with_scleroatrophy_of_the_extremities": 1,
    "Basan_syndrome": 2,
    "Adermatoglyphia": 1,
    "not_provided|Basan_syndrome|Keratoderma_with_scleroatrophy_of_the_extremities|Adermatoglyphia": 1,
    "SMARCAD1-related_disorder|Inborn_genetic_diseases": 1,
    "Brachydactyly|BMPR1B-related_disorder": 1,
    "Acromesomelic_dysplasia_3": 9,
    "BMPR1B-related_disorder": 3,
    "not_provided|Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Idiopathic_pulmonary_arterial_hypertension|BMPR1B-related_disorder": 1,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3": 52,
    "Inborn_genetic_diseases|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 8,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|Inborn_genetic_diseases": 2,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 88,
    "not_provided|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 3,
    "Type_A2_brachydactyly|Brachydactyly_type_A1D": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Pulmonary_hypertension|_primary|_3|Inborn_genetic_diseases": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Brachydactyly": 4,
    "not_provided|Type_A2_brachydactyly": 3,
    "Inborn_genetic_diseases|Type_A2_brachydactyly|Acromesomelic_dysplasia_3": 5,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|not_specified|not_provided": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|BMPR1B-related_disorder": 2,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|Brachydactyly_type_A1D|BMPR1B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 3,
    "BMPR1B-related_disorder|Brachydactyly|Type_A2_brachydactyly|Acromesomelic_dysplasia_3|not_specified|not_provided": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Inborn_genetic_diseases": 5,
    "not_provided|BMPR1B-related_disorder|Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 2,
    "Brachydactyly_type_A1D": 2,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|not_provided": 3,
    "not_provided|Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 1,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|BMPR1B-related_disorder": 1,
    "Acromesomelic_dysplasia_2B|Type_A2_brachydactyly|Acromesomelic_dysplasia_3|Brachydactyly_type_A1D": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Brachydactyly|not_provided": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Inborn_genetic_diseases|Brachydactyly": 1,
    "Inborn_genetic_diseases|Acromesomelic_dysplasia_3|Type_A2_brachydactyly|not_provided|Pulmonary_arterial_hypertension": 1,
    "not_provided|Type_A2_brachydactyly|Acromesomelic_dysplasia_3": 2,
    "Inborn_genetic_diseases|Pulmonary_arterial_hypertension|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 1,
    "BMPR1B-related_disorder|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 1,
    "Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly|not_provided": 2,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|not_provided": 2,
    "BMPR1B-related_disorder|Inborn_genetic_diseases|Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly": 1,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|BMPR1B-related_disorder|not_provided": 1,
    "BMPR1B-related_disorder|not_provided|Type_A2_brachydactyly|Acromesomelic_dysplasia_3": 1,
    "Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 2,
    "Brachydactyly|Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Inborn_genetic_diseases": 1,
    "Type_A2_brachydactyly|Acromesomelic_dysplasia_3|Brachydactyly_type_A1D": 1,
    "BMPR1B-related_disorder|Type_A2_brachydactyly|Acromesomelic_dysplasia_3": 1,
    "Acromesomelic_dysplasia_3|Type_A2_brachydactyly|Brachydactyly_type_A1D|Brachydactyly": 1,
    "BMPR1B-related_disorder|Type_A2_brachydactyly": 1,
    "Brachydactyly|Type_A2_brachydactyly|Acromesomelic_dysplasia_3": 1,
    "Brachydactyly|not_provided|not_specified": 1,
    "Brachydactyly|not_provided": 17,
    "UNC5C-related_disorder": 19,
    "not_provided|UNC5C-related_disorder": 4,
    "UNC5C-related_disorder|not_provided": 1,
    "Azoospermia|Spermatogenic_failure_70|Oligosynaptic_infertility": 1,
    "Alfadhel_syndrome": 3,
    "RAP1GDS1-related_disorder": 1,
    "EIF4E-related_disorder": 3,
    "Autism|_susceptibility_to|_19": 1,
    "AMED_syndrome|_digenic": 5,
    "Alcohol_dependence": 4,
    "Alcohol_dependence|Aerodigestive_tract_cancer|_squamous_cell|_alcohol-related|_protection_against": 1,
    "Parkinson_disease|_mitochondrial": 1,
    "ADH7-related_disorder|not_specified": 1,
    "ADH7-related_disorder": 11,
    "not_provided|TRMT10A-related_disorder|not_specified": 1,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1": 8,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1|not_specified|TRMT10A-related_disorder|not_provided": 1,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1|not_provided|Inborn_genetic_diseases": 1,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1|not_provided|not_specified": 1,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1|not_provided": 1,
    "Abnormality_of_the_nervous_system|not_provided": 2,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1|not_provided|See_cases": 1,
    "TRMT10A-related_disorder|not_specified|not_provided": 1,
    "TRMT10A-related_disorder|not_provided": 1,
    "not_provided|TRMT10A-related_disorder": 1,
    "Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1|not_specified|not_provided": 1,
    "not_provided|Microcephaly|_short_stature|_and_impaired_glucose_metabolism_1": 1,
    "not_specified|not_provided|Abetalipoproteinaemia": 5,
    "not_provided|Abetalipoproteinaemia": 58,
    "MTTP-related_disorder|not_specified|not_provided|Abetalipoproteinaemia": 2,
    "Abetalipoproteinaemia": 158,
    "MTTP-related_disorder": 4,
    "Abetalipoproteinaemia|Inborn_genetic_diseases": 2,
    "Abetalipoproteinaemia|not_provided": 50,
    "Abetalipoproteinaemia|MTTP-related_disorder|not_provided": 3,
    "Abetalipoproteinaemia|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|MTTP-related_disorder|Abetalipoproteinaemia": 1,
    "not_provided|Abetalipoproteinaemia|Inborn_genetic_diseases": 3,
    "not_provided|Abetalipoproteinaemia|not_specified": 5,
    "Abetalipoproteinaemia|Metabolic_syndrome_X|not_provided": 2,
    "MTTP-related_disorder|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Abetalipoproteinaemia": 2,
    "not_specified|Abetalipoproteinaemia|not_provided": 6,
    "Abetalipoproteinaemia|Metabolic_syndrome_X|not_provided|not_specified|METABOLIC_SYNDROME|_PROTECTION_AGAINST": 1,
    "Abetalipoproteinaemia|not_provided|MTTP-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Abetalipoproteinaemia": 3,
    "not_provided|MTTP-related_disorder": 1,
    "Abetalipoproteinaemia|MTTP-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Abetalipoproteinaemia|not_provided": 7,
    "not_provided|Abetalipoproteinaemia|Metabolic_syndrome_X": 2,
    "Abetalipoproteinaemia|not_provided|Metabolic_syndrome_X": 1,
    "not_provided|Metabolic_syndrome_X|Abetalipoproteinaemia": 1,
    "Abetalipoproteinaemia|not_specified|not_provided": 3,
    "Abetalipoproteinaemia|not_specified": 1,
    "not_provided|Abetalipoproteinaemia|MTTP-related_disorder": 1,
    "Retinal_disorders|not_specified|Abetalipoproteinaemia|not_provided": 1,
    "MTTP-related_disorder|Abetalipoproteinaemia|not_provided": 1,
    "MTTP-related_disorder|Inborn_genetic_diseases|Abetalipoproteinaemia|not_provided": 1,
    "not_provided|not_specified|Abetalipoproteinaemia": 1,
    "DAPP1-related_condition": 1,
    "PPP3CA-related_disorder": 5,
    "Developmental_and_epileptic_encephalopathy_91|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development": 13,
    "Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_91": 20,
    "not_provided|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91": 7,
    "Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development": 3,
    "Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91|not_provided": 6,
    "Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_91|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|not_provided": 8,
    "Developmental_and_epileptic_encephalopathy_91|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|PPP3CA-related_disorder|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy_91|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development": 13,
    "Developmental_and_epileptic_encephalopathy_91|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy_91": 3,
    "Inborn_genetic_diseases|not_provided|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91": 1,
    "Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91": 1,
    "not_provided|PPP3CA-related_disorder": 3,
    "Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91|Epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy_91|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy_91|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development": 1,
    "PPP3CA-related_disorder|not_provided|Arthrogryposis|_cleft_palate|_craniosynostosis|_and_impaired_intellectual_development|Developmental_and_epileptic_encephalopathy_91": 1,
    "PPP3CA-related_disorder|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy_91|Inborn_genetic_diseases|Seizure|Intellectual_disability": 1,
    "not_provided|PPP3CA-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Systemic_lupus_erythematosus": 1,
    "SLC39A8-related_disorder": 3,
    "SLC39A8-CDG": 15,
    "not_provided|Inflammatory_bowel_disease_1": 2,
    "SLC39A8-related_disorder|Inborn_genetic_diseases|not_provided|SLC39A8-CDG": 1,
    "SLC39A8-CDG|not_provided": 5,
    "SLC39A8-CDG|not_provided|Inborn_genetic_diseases": 1,
    "SLC39A8-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|SLC39A8-related_disorder": 1,
    "not_specified|SLC39A8-CDG|not_provided": 1,
    "not_provided|SLC39A8-related_disorder": 1,
    "not_provided|Immunodeficiency|_common_variable|_12": 11,
    "NFKB1-related_disorder": 9,
    "Immunodeficiency|_common_variable|_12": 34,
    "Immunodeficiency|_common_variable|_12|not_provided": 21,
    "Common_variable_immunodeficiency|Immunodeficiency|_common_variable|_12": 1,
    "Common_variable_immunodeficiency": 221,
    "Inherited_Immunodeficiency_Diseases|not_provided": 5,
    "NFKB1-related_disorder|not_provided": 7,
    "not_provided|NFKB1-related_disorder": 9,
    "Common_variable_immunodeficiency|not_provided": 5,
    "Common_variable_immunodeficiency|Inherited_Immunodeficiency_Diseases|Immunodeficiency|_common_variable|_12|not_provided": 1,
    "Inherited_Immunodeficiency_Diseases|Immunodeficiency|_common_variable|_12|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_12": 1,
    "not_specified|Immunodeficiency|_common_variable|_12|not_provided": 1,
    "Immunodeficiency|_common_variable|_12|not_provided|Inborn_genetic_diseases": 1,
    "Common_variable_immunodeficiency|Inherited_Immunodeficiency_Diseases": 1,
    "not_provided|Immunodeficiency|_common_variable|_12|Inborn_genetic_diseases": 1,
    "Inherited_Immunodeficiency_Diseases|Immunodeficiency|_common_variable|_12": 1,
    "NFKB1-related_disorder|not_provided|Immunodeficiency|_common_variable|_12": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_12": 1,
    "Immunodeficiency|_common_variable|_12|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency|_common_variable|_12": 1,
    "Beta-D-mannosidosis": 565,
    "not_provided|Beta-D-mannosidosis": 34,
    "not_provided|Beta-D-mannosidosis|MANBA-related_disorder": 5,
    "Beta-D-mannosidosis|Inborn_genetic_diseases": 16,
    "not_specified|not_provided|Beta-D-mannosidosis": 3,
    "Beta-D-mannosidosis|not_provided": 2,
    "Inborn_genetic_diseases|Beta-D-mannosidosis": 20,
    "Beta-D-mannosidosis|not_specified|not_provided": 2,
    "Intellectual_disability|Beta-D-mannosidosis": 1,
    "not_specified|Beta-D-mannosidosis|not_provided": 1,
    "Inborn_genetic_diseases|Beta-D-mannosidosis|not_provided": 2,
    "Beta-D-mannosidosis|MANBA-related_disorder": 8,
    "MANBA-related_disorder|Beta-D-mannosidosis": 4,
    "not_provided|Beta-D-mannosidosis|Hearing_impairment": 1,
    "not_provided|not_specified|Beta-D-mannosidosis": 2,
    "Meniere_disease|Intellectual_disability|not_provided|Beta-D-mannosidosis": 1,
    "Meniere_disease|Beta-D-mannosidosis|MANBA-related_disorder|not_provided": 1,
    "Beta-D-mannosidosis|Meniere_disease": 1,
    "Beta-D-mannosidosis|Intellectual_disability": 1,
    "Hearing_impairment|not_provided|Beta-D-mannosidosis": 1,
    "Beta-D-mannosidosis|not_specified": 2,
    "Beta-D-mannosidosis|Meniere_disease|not_specified": 1,
    "Inborn_genetic_diseases|MANBA-related_disorder|Beta-D-mannosidosis": 1,
    "MANBA-related_disorder": 2,
    "MANBA-related_disorder|Inborn_genetic_diseases|not_provided|Beta-D-mannosidosis": 1,
    "Beta-D-mannosidosis|Inborn_genetic_diseases|not_provided": 1,
    "Wolfram_syndrome_2": 12,
    "Wolfram_syndrome_2|Inborn_genetic_diseases": 2,
    "CISD2-related_disorder|not_provided": 2,
    "Wolfram_syndrome_2|not_provided": 3,
    "Inborn_genetic_diseases|Wolfram_syndrome_2|not_provided": 1,
    "Wolfram_syndrome_2|CISD2-related_disorder|not_provided": 1,
    "not_provided|CISD2-related_disorder": 1,
    "not_provided|Wolfram_syndrome_2": 3,
    "Wolfram_syndrome_2|not_specified|not_provided": 1,
    "not_provided|CENPE-related_disorder": 8,
    "CENPE-related_disorder": 9,
    "CENPE-related_disorder|not_specified": 1,
    "not_specified|Microcephaly_13|_primary|_autosomal_recessive": 3,
    "CENPE-related_disorder|not_provided": 2,
    "CENPE-related_disorder|not_specified|not_provided": 3,
    "Microcephaly_13|_primary|_autosomal_recessive": 10,
    "not_specified|CENPE-related_disorder": 2,
    "Microcephaly_13|_primary|_autosomal_recessive|not_provided": 2,
    "not_provided|CENPE-related_disorder|not_specified": 1,
    "not_provided|Microcephaly_13|_primary|_autosomal_recessive": 4,
    "Microcephaly_13|_primary|_autosomal_recessive|not_specified": 1,
    "not_provided|not_specified|Microcephaly_13|_primary|_autosomal_recessive": 1,
    "CENPE-related_disorder|not_provided|not_specified": 1,
    "Microcephaly_13|_primary|_autosomal_recessive|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 22,
    "not_provided|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 9,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|not_provided|TACR3-related_disorder": 1,
    "not_provided|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|not_specified": 2,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|not_provided": 2,
    "not_specified|TACR3-related_disorder|not_provided|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 1,
    "TACR3-related_disorder|not_provided": 1,
    "not_provided|TACR3-related_disorder": 2,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|not_specified|not_provided": 2,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|TACR3-related_disorder|not_provided": 1,
    "TACR3-related_disorder": 3,
    "Hypogonadotropic_hypogonadism|TACR3-related_disorder|not_provided|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|Autism_spectrum_disorder": 1,
    "not_provided|TACR3-related_disorder|Hypogonadotropic_hypogonadism_11_with_or_without_anosmia": 1,
    "not_specified|TACR3-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_11_with_or_without_anosmia|not_specified": 1,
    "TET2-related_disorder": 12,
    "TET2-related_disorder|not_specified": 2,
    "TET2-related_disorder|not_specified|not_provided": 7,
    "not_provided|Immunodeficiency_75": 3,
    "TET2-related_disorder|not_provided": 6,
    "Immunodeficiency_75|Myelodysplastic_syndrome": 1,
    "not_specified|TET2-related_disorder": 2,
    "Immunodeficiency_75|not_specified|not_provided": 1,
    "not_specified|not_provided|TET2-related_disorder": 1,
    "not_provided|Immunodeficiency_75|not_specified": 2,
    "not_specified|TET2-related_disorder|not_provided": 2,
    "not_specified|Multiple_myeloma": 1,
    "Immunodeficiency_75": 7,
    "Immunodeficiency_75|not_specified": 1,
    "not_provided|TET2-related_disorder": 3,
    "not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 9,
    "not_provided|not_specified|TET2-related_disorder": 3,
    "Myelodysplastic_syndrome|Immunodeficiency_75|EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_provided": 1,
    "TET2-related_disorder|not_provided|Immunodeficiency_75": 1,
    "Myelodysplastic_syndrome|Immunodeficiency_75|not_provided|not_specified": 1,
    "Clonal_hematopoiesis": 1,
    "not_provided|Angioimmunoblastic_T-cell_lymphoma": 2,
    "not_provided|Atypical_chronic_myeloid_leukemia|_BCR-ABL1_negative": 1,
    "Myelodysplastic_syndrome|Immunodeficiency_75|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "not_provided|Immunodeficiency_75|Myelodysplastic_syndrome": 1,
    "Immunodeficiency_75|not_provided|Angioimmunoblastic_T-cell_lymphoma": 1,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|Atypical_chronic_myeloid_leukemia|_BCR-ABL1_negative|not_provided": 1,
    "Immunodeficiency_75|not_provided": 1,
    "Sudden_cardiac_failure|_infantile|Sudden_cardiac_failure|_alcohol-induced|not_provided": 2,
    "Sudden_cardiac_failure|_infantile": 8,
    "mitochondrial_cardiomyopathy_and_sudden_cardiac_failure|not_provided": 1,
    "not_specified|not_provided|Sudden_cardiac_failure|_infantile": 1,
    "Sudden_cardiac_failure|_alcohol-induced|Sudden_cardiac_failure|_infantile": 3,
    "Sudden_cardiac_failure|_infantile|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Sudden_cardiac_failure|_infantile": 2,
    "not_provided|Sudden_cardiac_failure|_alcohol-induced|Inborn_genetic_diseases|Sudden_cardiac_failure|_infantile": 1,
    "not_provided|PPA2-related_disorder": 3,
    "Sudden_cardiac_failure|_infantile|Sudden_cardiac_failure|_alcohol-induced": 2,
    "not_provided|Sudden_cardiac_failure|_alcohol-induced": 1,
    "not_provided|Sudden_cardiac_failure|_alcohol-induced|Inborn_genetic_diseases|Sudden_cardiac_failure|_infantile|Cardiovascular_phenotype": 1,
    "Sudden_cardiac_failure|_alcohol-induced|Sudden_cardiac_failure|_infantile|PPA2-related_disorder": 1,
    "not_provided|Sudden_cardiac_failure|_infantile|Sudden_cardiac_failure|_alcohol-induced": 3,
    "sudden_cardiac_failure|Cardiomyopathy|_mitochondrial": 1,
    "Sudden_cardiac_failure|_infantile|Sudden_cardiac_failure|_alcohol-induced|Inborn_genetic_diseases|not_provided": 1,
    "Sudden_cardiac_failure|_alcohol-induced|Sudden_cardiac_failure|_infantile|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PPA2-related_disorder": 2,
    "Sudden_cardiac_failure|_infantile|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Bilateral_renal_agenesis": 1,
    "TBCK-related_disorder|not_provided": 10,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|not_provided": 28,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 17,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|Inborn_genetic_diseases|not_provided": 4,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 41,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|TBCK-related_disorder|not_provided": 1,
    "not_provided|TBCK-related_disorder|Inborn_genetic_diseases": 2,
    "TBCK-related_disorder": 6,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|not_provided|Abnormality_of_the_nervous_system|Global_developmental_delay|Seizure|Hypotonia|Ventral_septal_defect|Delayed_reflexes|Dysmorphism": 1,
    "not_provided|TBCK-related_disorder": 8,
    "not_provided|Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 2,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|Syndromic_Infantile_Encephalopathy": 1,
    "TBCK-related_disorder|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|Syndromic_Infantile_Encephalopathy": 1,
    "TBCK-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Global_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|TBCK-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|TBCK-related_disorder|not_provided": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|not_provided": 1,
    "TBCK-related_disorder|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 1,
    "Neurodevelopmental_disorder|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 1,
    "Inborn_genetic_diseases|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3|Syndromic_Infantile_Encephalopathy": 1,
    "Abnormality_of_the_nervous_system|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_3": 1,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 2,
    "TBCK-related_disorder|not_specified|not_provided": 1,
    "AIMP1-related_disorder": 2,
    "not_provided|Hypomyelinating_leukodystrophy_3": 4,
    "Hypomyelinating_leukodystrophy_3|not_provided|AIMP1-related_disorder": 1,
    "not_provided|AIMP1-related_disorder|Hypomyelinating_leukodystrophy_3": 1,
    "Hypomyelinating_leukodystrophy_3": 9,
    "not_provided|AIMP1-related_disorder": 1,
    "Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_3": 1,
    "AIMP1-related_disorder|not_provided": 2,
    "AIMP1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PAPSS1-related_disorder": 2,
    "Calvarial_doughnut_lesions_with_bone_fragility_with_or_without_spondylometaphyseal_dysplasia|Calvarial_doughnut_lesions-bone_fragility_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|SGMS2-related_disorder|Calvarial_doughnut_lesions-bone_fragility_syndrome": 1,
    "Calvarial_doughnut_lesions_with_bone_fragility_and_spondylometaphyseal_dysplasia": 2,
    "SGMS2-related_disorder": 1,
    "SGMS2-related_disorder|not_provided": 2,
    "Calvarial_doughnut_lesions-bone_fragility_syndrome": 3,
    "Calvarial_doughnut_lesions-bone_fragility_syndrome|not_provided": 2,
    "SGMS2-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_56": 26,
    "Spastic_paraplegia|CYP2U1-related_disorder|not_specified|not_provided": 1,
    "CYP2U1-related_disorder": 2,
    "Hereditary_spastic_paraplegia_56|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_56|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_56|Spastic_paraplegia": 6,
    "Hereditary_spastic_paraplegia_5A": 25,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_56": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|not_provided": 5,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_56": 1,
    "Intellectual_disability|Lower_limb_spasticity|Seizure": 1,
    "Hereditary_spastic_paraplegia_56|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "CYP2U1-related_disorder|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_56|not_provided": 3,
    "Spastic_paraplegia|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "CYP2U1-related_disorder|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_56|Neurodegeneration|Global_developmental_delay": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|CYP2U1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_56|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|CYP2U1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 16,
    "Spastic_paraplegia|See_cases|Hereditary_spastic_paraplegia_56": 1,
    "CYP2U1-related_disorder|Hereditary_spastic_paraplegia_56|not_provided|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_56|Spastic_paraplegia|CYP2U1-related_disorder": 1,
    "not_specified|Spastic_paraplegia|not_provided": 15,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_56|Hereditary_spastic_paraplegia": 1,
    "CYP2U1-related_disorder|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_4": 8,
    "Hyperinsulinemic_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 3,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 5,
    "Hyperinsulinemic_hypoglycemia": 2,
    "not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4": 3,
    "Hyperinsulinism|_Dominant/Recessive|Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 3,
    "not_provided|Hyperinsulinemic_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 1,
    "Hyperinsulinism|_Dominant/Recessive|not_specified|not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|not_provided|Hyperinsulinemic_hypoglycemia": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|Hyperinsulinemic_hypoglycemia": 12,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 7,
    "HADH-related_disorder": 10,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 181,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|Monogenic_diabetes": 2,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Inborn_genetic_diseases": 3,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|HADH-related_disorder|Hyperinsulinemic_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_4": 1,
    "Inborn_genetic_diseases|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 4,
    "not_specified|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|Hyperinsulinemic_hypoglycemia": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 4,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|not_provided": 4,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4": 5,
    "Hyperinsulinemic_hypoglycemia|not_specified|HADH-related_disorder|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|not_provided": 1,
    "HADH-related_disorder|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|not_provided": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|HADH-related_disorder|Hyperinsulinemic_hypoglycemia": 1,
    "not_specified|not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 1,
    "Hyperinsulinemic_hypoglycemia|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 9,
    "Monogenic_diabetes|Inborn_genetic_diseases|not_specified|not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinism|_Dominant/Recessive|Hyperinsulinemic_hypoglycemia": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|HADH-related_disorder|Hyperinsulinemic_hypoglycemia": 1,
    "not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|Hyperinsulinemic_hypoglycemia": 1,
    "not_specified|Abnormal_brain_morphology": 1,
    "Hyperinsulinemic_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_4|not_provided": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia|_familial|_4": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia": 1,
    "not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 2,
    "HADH-related_disorder|Monogenic_diabetes|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|not_specified|not_provided": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|not_provided|Hyperinsulinemic_hypoglycemia": 1,
    "HADH-related_disorder|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 2,
    "Hyperinsulinemic_hypoglycemia|not_specified|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 1,
    "HADH-related_disorder|Monogenic_diabetes|Hyperinsulinemic_hypoglycemia|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|not_specified": 1,
    "Hyperinsulinemic_hypoglycemia|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified|Hyperinsulinemic_hypoglycemia|_familial|_4|not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 1,
    "HADH-related_disorder|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|not_specified|Hyperinsulinemic_hypoglycemia|Monogenic_diabetes|not_provided": 1,
    "Monogenic_diabetes|not_specified|not_provided|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Familial_hyperinsulinism|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 1,
    "Hyperinsulinemic_hypoglycemia|Monogenic_diabetes": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Hyperinsulinemic_hypoglycemia": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|Hyperinsulinemic_hypoglycemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 1,
    "HADH-related_disorder|Hyperinsulinemic_hypoglycemia|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase": 1,
    "Hyperinsulinemic_hypoglycemia|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia|_familial|_4|not_specified|not_provided|Monogenic_diabetes": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_4|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Inborn_genetic_diseases|Hyperinsulinemic_hypoglycemia": 1,
    "not_provided|not_specified|Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinemic_hypoglycemia": 1,
    "Deficiency_of_3-hydroxyacyl-CoA_dehydrogenase|Hyperinsulinism|_Dominant/Recessive": 1,
    "ECTODERMAL_DYSPLASIA_17_WITH_OR_WITHOUT_LIMB_MALFORMATIONS|Ectrodactyly": 2,
    "Abnormal_radial_ray_morphology|ECTODERMAL_DYSPLASIA_17_WITH_OR_WITHOUT_LIMB_MALFORMATIONS": 1,
    "ECTODERMAL_DYSPLASIA_17_WITH_OR_WITHOUT_LIMB_MALFORMATIONS": 1,
    "LEF1-related_disorder": 1,
    "Syndromic_disease": 5,
    "Ectrodactyly_and_ectodermal_dysplasia_without_cleft_lip/palate": 1,
    "OSTC-related_Disorders": 1,
    "COL25A1-related_disorder": 11,
    "Fibrosis_of_extraocular_muscles|_congenital|_5": 8,
    "COL25A1-related_disorder|not_provided": 2,
    "not_provided|COL25A1-related_disorder": 2,
    "Arthrogryposis|Fibrosis_of_extraocular_muscles|_congenital|_5": 1,
    "Inborn_genetic_diseases|Fibrosis_of_extraocular_muscles|_congenital|_5": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 9,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder": 5,
    "Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder": 2,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|not_provided": 5,
    "CFI-related_disorder": 107,
    "CFI-related_disorder|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|CFI-related_disorder": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency": 7,
    "not_specified|Atypical_hemolytic-uremic_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13": 35,
    "CFI-related_disorder|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 3,
    "Age_related_macular_degeneration_13": 2,
    "not_provided|CFI-related_disorder": 14,
    "not_specified|CFI-related_disorder|not_provided": 2,
    "not_provided|Factor_I_deficiency": 4,
    "Kidney_disorder|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|not_provided": 2,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency": 1,
    "CFI-related_disorder|not_provided": 21,
    "CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 3,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|CFI-related_disorder|not_specified|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 4,
    "Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Afibrinogenemia|Inborn_genetic_diseases|not_provided": 1,
    "Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided": 5,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|CFI-related_disorder": 2,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|not_provided": 3,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|CFI-related_disorder": 4,
    "Factor_I_deficiency|not_provided|CFI-related_disorder": 1,
    "not_provided|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13": 2,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|not_specified|not_provided": 1,
    "Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_specified|not_provided|CFI-related_disorder": 1,
    "CFI-related_disorder|Age_related_macular_degeneration_13|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided": 1,
    "Inborn_genetic_diseases|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided": 1,
    "Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "Factor_I_deficiency|not_provided": 4,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome|not_provided": 2,
    "not_specified|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|Thrombotic_microangiopathy|Inborn_genetic_diseases|not_provided|CFI-related_disorder": 1,
    "CFI-related_disorder|not_provided|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|CFI-related_disorder": 1,
    "CFI-related_disorder|Factor_I_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|CFI-related_disorder|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|Macular_degeneration|_age-related|_13|_susceptibility_to|not_provided": 1,
    "Factor_I_deficiency|CFI-related_disorder|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|not_provided": 2,
    "Focal_segmental_glomerulosclerosis|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder": 1,
    "CFI-related_disorder|not_provided|Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 2,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome": 2,
    "Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided|CFI-related_disorder": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome": 2,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|C3_glomerulonephritis|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|CFI-related_disorder|not_specified": 1,
    "CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome|Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided|CFI-related_disorder": 1,
    "Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|Age_related_macular_degeneration_13|not_provided": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|not_specified|not_provided": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|CFI-related_disorder": 1,
    "not_provided|not_specified|C3_glomerulonephritis": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|CFI-related_disorder|not_provided": 4,
    "Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|not_provided": 1,
    "CFI-related_disorder|not_provided|Factor_I_deficiency": 2,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided|CFI-related_disorder": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13": 4,
    "not_specified|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|Inborn_genetic_diseases|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided|CFI-related_disorder": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|CFI-related_disorder|not_provided": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|not_provided": 2,
    "not_specified|Factor_I_deficiency|CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "Factor_I_deficiency|CFI-related_disorder|not_provided": 2,
    "Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|CFI-related_disorder|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Chronic_kidney_disease": 1,
    "not_provided|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency": 2,
    "Factor_I_deficiency|CFI-related_disorder|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided": 1,
    "Factor_I_deficiency": 4,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency": 1,
    "not_provided|not_specified|Atypical_hemolytic-uremic_syndrome": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Atypical_hemolytic-uremic_syndrome|not_provided|not_specified": 1,
    "Factor_I_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|not_provided|CFI-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|not_provided": 1,
    "CFI-related_disorder|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|not_provided|C3_glomerulonephritis": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|CFI-related_disorder|Atypical_hemolytic-uremic_syndrome|not_specified": 1,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "not_specified|not_provided|CFI-related_disorder|Atypical_hemolytic-uremic_syndrome": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|not_provided": 1,
    "CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency": 1,
    "not_provided|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Factor_I_deficiency|Kidney_failure|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|Macular_degeneration|_age-related|_13|_susceptibility_to|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|not_provided|Inborn_genetic_diseases": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|CFI-related_disorder|not_provided": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|not_provided": 2,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Age_related_macular_degeneration_13|Inborn_genetic_diseases|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Age_related_macular_degeneration_13|not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|Peroxisome_biogenesis_disorder_4A_(Zellweger)|CFI-related_disorder": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Factor_I_deficiency|Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_13|Factor_I_deficiency|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|CFI-related_disorder": 1,
    "Age_related_macular_degeneration_13|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Factor_I_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_I_factor_anomaly|Age_related_macular_degeneration_13|Factor_I_deficiency|Complement-mediated_glomerular_disease|CFI-related_disorder": 1,
    "Factor_I_deficiency|C3_glomerulonephritis": 1,
    "GAR1-related_disorder": 1,
    "Congenital_Stationary_Night_Blindness|_Recessive|not_provided": 15,
    "Congenital_stationary_night_blindness_1F|not_provided|LRIT3-related_disorder": 1,
    "not_provided|Congenital_stationary_night_blindness_1F": 8,
    "LRIT3-related_disorder|not_provided": 1,
    "not_specified|Congenital_stationary_night_blindness_1F|not_provided": 1,
    "not_provided|LRIT3-related_disorder": 3,
    "not_provided|Congenital_stationary_night_blindness_1F|LRIT3-related_disorder": 1,
    "Congenital_Stationary_Night_Blindness|_Recessive|not_provided|not_specified": 1,
    "Congenital_stationary_night_blindness_1F|not_provided": 7,
    "Congenital_stationary_night_blindness_1F|not_provided|LRIT3-related_disorder|Optic_atrophy": 1,
    "not_provided|Congenital_stationary_night_blindness_1F|not_specified|Congenital_Stationary_Night_Blindness|_Recessive": 1,
    "LRIT3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_Stationary_Night_Blindness|_Recessive|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_1F|not_provided": 2,
    "Congenital_stationary_night_blindness_1F": 31,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1F|Congenital_Stationary_Night_Blindness|_Recessive": 1,
    "not_provided|Congenital_stationary_night_blindness_1F|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Congenital_stationary_night_blindness_1F": 1,
    "not_provided|Congenital_stationary_night_blindness_1F|not_specified|LRIT3-related_disorder": 1,
    "not_specified|not_provided|Congenital_Stationary_Night_Blindness|_Recessive": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_stationary_night_blindness_1F": 1,
    "Congenital_stationary_night_blindness_1F|not_specified|not_provided": 1,
    "Congenital_stationary_night_blindness_1F|Inborn_genetic_diseases|not_provided|LRIT3-related_disorder": 1,
    "not_provided|Congenital_Stationary_Night_Blindness|_Recessive": 4,
    "Congenital_stationary_night_blindness_1F|Congenital_Stationary_Night_Blindness|_Recessive|not_provided": 1,
    "Congenital_stationary_night_blindness_1F|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_Stationary_Night_Blindness|_Recessive": 27,
    "Renal_hypomagnesemia_4": 59,
    "Renal_hypomagnesemia_4|not_provided": 39,
    "not_provided|Cholangiocarcinoma|Renal_hypomagnesemia_4": 1,
    "not_provided|Renal_hypomagnesemia_4": 20,
    "Hereditary_renal_cell_carcinoma|Renal_hypomagnesemia_4|not_provided": 1,
    "EGF-related_disorder|Renal_hypomagnesemia_4|not_provided": 4,
    "not_specified|not_provided|Renal_hypomagnesemia_4": 4,
    "Renal_hypomagnesemia_4|EGF-related_disorder|not_provided|not_specified": 1,
    "not_specified|Renal_hypomagnesemia_4|not_provided": 3,
    "EGF-related_disorder": 2,
    "Renal_hypomagnesemia_4|not_specified": 1,
    "not_specified|not_provided|EGF-related_disorder": 1,
    "Renal_hypomagnesemia_4|not_provided|EGF-related_disorder": 1,
    "EGF-related_disorder|not_provided": 2,
    "EGF-related_disorder|not_provided|Renal_hypomagnesemia_4": 1,
    "not_provided|Renal_hypomagnesemia_4|EGF-related_disorder": 6,
    "not_provided|EGF-related_disorder": 1,
    "not_provided|EGF-related_disorder|Renal_hypomagnesemia_4": 1,
    "Renal_hypomagnesemia_4|not_specified|not_provided": 1,
    "Renal_Hypomagnesemia|_Recessive|EGF-related_disorder|not_provided": 1,
    "Cataract|Irido-corneo-trabecular_dysgenesis|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Axenfeld-Rieger_syndrome_type_1": 2,
    "Cataract|Anterior_segment_dysgenesis_4|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1": 2,
    "Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1": 4,
    "PITX2-related_disorder": 11,
    "not_provided|Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1": 1,
    "PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|not_provided|Cataract|Ring_dermoid_of_cornea|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_1|Hypoplasia_of_the_iris": 1,
    "Irido-corneo-trabecular_dysgenesis|Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Axenfeld-Rieger_syndrome_type_1": 5,
    "Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Anterior_segment_dysgenesis_1|PITX2-Related_Eye_Abnormalities|Axenfeld-Rieger_syndrome|Irido-corneo-trabecular_dysgenesis": 1,
    "Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_1|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1": 2,
    "Irido-corneo-trabecular_dysgenesis|Cataract|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities": 1,
    "Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Inborn_genetic_diseases": 2,
    "Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1": 12,
    "Axenfeld-Rieger_syndrome_type_1": 37,
    "PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris|Cataract|not_provided": 1,
    "Anterior_segment_dysgenesis_4|Axenfeld-Rieger_anomaly_with_partially_absent_eye_muscles|_distinctive_face|_hydrocephaly|_and_skeletal_abnormalities": 1,
    "PITX2-Related_Eye_Abnormalities|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Irido-corneo-trabecular_dysgenesis|not_specified|not_provided|Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_1|Hypoplasia_of_the_iris": 1,
    "Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4": 24,
    "PITX2-Related_Eye_Abnormalities|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris|not_provided|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_1|PITX2-related_disorder|Anterior_segment_dysgenesis_4|Irido-corneo-trabecular_dysgenesis|Cataract": 1,
    "Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Atrial_fibrillation|_familial|_1|Hypoplasia_of_the_iris|PITX2-related_disorder|PITX2-Related_Eye_Abnormalities|Cataract|Ring_dermoid_of_cornea": 1,
    "PITX2-Related_Eye_Abnormalities|not_specified|not_provided|Hypoplasia_of_the_iris|Axenfeld-Rieger_syndrome_type_1|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_1|Anterior_segment_dysgenesis_4|Irido-corneo-trabecular_dysgenesis|Cataract": 1,
    "PITX2-Related_Eye_Abnormalities|PITX2-related_disorder|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Irido-corneo-trabecular_dysgenesis|not_specified|not_provided|Cataract|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris": 1,
    "Inborn_genetic_diseases|Axenfeld-Rieger_syndrome_type_1": 1,
    "Axenfeld-Rieger_syndrome_type_1|not_provided|Anterior_segment_dysgenesis_4": 1,
    "Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|not_provided": 2,
    "ANTERIOR_SEGMENT_DYSGENESIS_4|_PETERS_ANOMALY_SUBTYPE": 1,
    "Cataract|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Anterior_segment_dysgenesis_1|Axenfeld-Rieger_syndrome|PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis": 1,
    "Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|not_provided": 1,
    "Anterior_segment_dysgenesis|Anterior_segment_dysgenesis_4": 1,
    "not_provided|Anterior_segment_dysgenesis_4": 1,
    "Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Inborn_genetic_diseases|Anterior_segment_dysgenesis|Ring_dermoid_of_cornea": 1,
    "Anterior_segment_dysgenesis_4": 1,
    "Rieger_anomaly": 3,
    "not_provided|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1": 1,
    "Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Irido-corneo-trabecular_dysgenesis|Intellectual_disability|Cataract|Anterior_segment_dysgenesis_1|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Ring_dermoid_of_cornea": 1,
    "not_provided|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|not_specified": 1,
    "PITX2-related_disorder|not_specified": 1,
    "not_specified|PITX2-related_disorder": 1,
    "Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|not_specified": 1,
    "PITX2-Related_Eye_Abnormalities|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Irido-corneo-trabecular_dysgenesis|not_specified|not_provided|Cataract|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris": 1,
    "Irido-corneo-trabecular_dysgenesis|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Cataract|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Ring_dermoid_of_cornea": 6,
    "Irido-corneo-trabecular_dysgenesis|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Cataract|PITX2-Related_Eye_Abnormalities|Hypoplasia_of_the_iris": 6,
    "Irido-corneo-trabecular_dysgenesis|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Cataract": 10,
    "Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Cataract|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Ring_dermoid_of_cornea": 1,
    "Irido-corneo-trabecular_dysgenesis|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Cataract|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities": 2,
    "Irido-corneo-trabecular_dysgenesis|not_provided|Ring_dermoid_of_cornea|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Cataract": 2,
    "Irido-corneo-trabecular_dysgenesis|not_provided|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Cataract|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Ring_dermoid_of_cornea": 2,
    "Irido-corneo-trabecular_dysgenesis|Axenfeld-Rieger_syndrome_type_1|Anterior_segment_dysgenesis_4|Cataract|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|not_provided|Ring_dermoid_of_cornea": 1,
    "Irido-corneo-trabecular_dysgenesis|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Cataract|PITX2-Related_Eye_Abnormalities|Ring_dermoid_of_cornea|Hypoplasia_of_the_iris": 1,
    "Irido-corneo-trabecular_dysgenesis|Anterior_segment_dysgenesis_4|Axenfeld-Rieger_syndrome_type_1|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Cataract|Ring_dermoid_of_cornea": 3,
    "Irido-corneo-trabecular_dysgenesis|Anterior_segment_dysgenesis_4|Ring_dermoid_of_cornea|Axenfeld-Rieger_syndrome_type_1|Hypoplasia_of_the_iris|PITX2-Related_Eye_Abnormalities|Cataract": 1,
    "ALPK1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "ALPK1-related_disorder|not_provided": 7,
    "ALPK1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Retinal_dystrophy|_optic_nerve_edema|_splenomegaly|_anhidrosis|_and_migraine_headache_syndrome": 1,
    "Retinal_dystrophy|_optic_nerve_edema|_splenomegaly|_anhidrosis|_and_migraine_headache_syndrome": 10,
    "ALPK1-related_disorder": 4,
    "ALPK1-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|_optic_nerve_edema|_splenomegaly|_anhidrosis|_and_migraine_headache_syndrome|not_provided": 1,
    "not_provided|ALPK1-related_disorder": 1,
    "Retinal_dystrophy|_optic_nerve_edema|_splenomegaly|_anhidrosis|_and_migraine_headache_syndrome|not_provided": 2,
    "ALPK1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Autism_spectrum_disorder|Childhood_apraxia_of_speech": 1,
    "See_cases|Progressive_muscle_weakness|Dysarthria|Dysphagia|Bowel_incontinence|Spastic_paraplegia|Difficulty_walking": 1,
    "Autism_spectrum_disorder|Childhood_apraxia_of_speech|not_specified": 1,
    "Microcephalic_primordial_dwarfism|_Alazami_type": 33,
    "LARP7-related_disorder|not_provided": 4,
    "not_provided|LARP7-related_disorder|Microcephalic_primordial_dwarfism|_Alazami_type": 1,
    "not_provided|Microcephalic_primordial_dwarfism|_Alazami_type": 5,
    "not_provided|LARP7-related_disorder": 1,
    "LARP7-related_disorder": 3,
    "not_specified|not_provided|Microcephalic_primordial_dwarfism|_Alazami_type": 2,
    "not_provided|Microcephalic_primordial_dwarfism|_Alazami_type|Inborn_genetic_diseases": 1,
    "Microcephalic_primordial_dwarfism|_Alazami_type|Intellectual_disability|not_provided": 1,
    "Microcephalic_primordial_dwarfism|_Alazami_type|not_provided": 4,
    "not_provided|LARP7-related_disorder|not_specified": 1,
    "Abnormal_brain_morphology|Microcephalic_primordial_dwarfism|_Alazami_type": 1,
    "Alazami-Yuan_syndrome|not_provided|Intellectual_disability|Epileptic_encephalopathy": 1,
    "not_specified|ANK2-related_disorder": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related": 64,
    "not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Autism_spectrum_disorder": 1,
    "Cardiovascular_phenotype|Meniere_disease": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome": 4,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Long_QT_syndrome": 5,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_provided": 3,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 17,
    "ANK2-related_disorder": 20,
    "not_provided|ANK2-related_disorder": 3,
    "ANK2-related_Autism": 2,
    "Cardiovascular_phenotype|not_provided|ANK2-related_disorder|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 7,
    "ANK2-related_disorder|not_provided": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|ANK2-related_disorder": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 18,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 57,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "ANK2-related_disorder|not_provided|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 14,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_provided": 1,
    "not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 2,
    "ANK2-associated_Neurodevelopmental_Disorder|Long_QT_syndrome": 1,
    "not_provided|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Intellectual_disability|not_specified": 18,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 8,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 29,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 3,
    "Brugada_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 3,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 4,
    "Wolff-Parkinson-White_pattern|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 7,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Long_QT_syndrome": 2,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 6,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Cardiovascular_phenotype": 6,
    "not_provided|Brugada_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 4,
    "Cardiovascular_phenotype|not_specified|ANK2-related_disorder|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 6,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 4,
    "not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 5,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified": 2,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder": 1,
    "Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_specified|ANK2-related_disorder": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified": 1,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified": 2,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|ANK2-related_disorder": 2,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 3,
    "Torsades_de_pointes|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Wolff-Parkinson-White_pattern|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 6,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_specified": 1,
    "Long_QT_syndrome|not_specified|not_provided": 10,
    "ANK2-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_provided": 5,
    "Long_QT_syndrome|ANK2-related_disorder|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder": 1,
    "not_specified|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome": 1,
    "ANK2-related_disorder|Long_QT_syndrome": 2,
    "Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 3,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 11,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 9,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 3,
    "Torsades_de_pointes": 1,
    "ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 27,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified|not_provided": 1,
    "Channelopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|ANK2-related_disorder|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "Cardiovascular_phenotype|Ventricular_tachycardia|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|ANK2-related_disorder|not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_provided|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 4,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_specified|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|ANK2-related_disorder|Cardiovascular_phenotype|Complex_neurodevelopmental_disorder": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|not_specified|ANK2-related_disorder|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 3,
    "not_provided|Long_QT_syndrome|not_specified": 3,
    "Cardiovascular_phenotype|not_provided|ANK2-related_disorder|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Conduction_disorder_of_the_heart|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Long_QT_syndrome": 3,
    "Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome": 6,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 4,
    "Long_QT_syndrome|ANK2-related_disorder|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 13,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided": 1,
    "ANK2-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "ANK2-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome": 3,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Inborn_genetic_diseases": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "not_specified|ANK2-related_disorder|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|ANK2-associated_Neurodevelopmental_Disorder": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 12,
    "not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|Cardiac_arrhythmia|not_provided": 10,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|not_specified": 1,
    "Long_QT_syndrome|not_provided|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 3,
    "Long_QT_syndrome|ANK2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 4,
    "Cardiovascular_phenotype|ANK2-related_disorder|Long_QT_syndrome": 1,
    "Meniere_disease|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_4|Cardiac_arrhythmia|_ankyrin-B-related|Autism_spectrum_disorder|not_specified|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congestive_heart_failure|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Cardiovascular_phenotype": 7,
    "Long_QT_syndrome|See_cases|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome|not_specified": 1,
    "ANK2-associated_disorder": 2,
    "not_specified|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder": 1,
    "Conduction_disorder_of_the_heart|not_specified|Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified": 3,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified": 1,
    "ANK2-related_disorder|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|ANK2-related_disorder": 2,
    "Long_QT_syndrome|Long_QT_syndrome_4": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|not_specified": 5,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 5,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 3,
    "Long_QT_syndrome|ANK2-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Intellectual_disability|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided|ANK2-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrest|not_provided|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|ANK2-related_disorder|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome_2": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified|not_provided": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Long_QT_syndrome|ANK2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "Hypertrophic_cardiomyopathy|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|Brugada_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiac_arrest": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|ANK2-related_disorder": 1,
    "Cardiovascular_phenotype|ANK2-related_disorder|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 3,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiomyopathy": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_provided": 3,
    "ANK2-associated_Complex_Neurodevelopmental_Disorder|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 3,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Intellectual_disability": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Long_QT_syndrome|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome|Conduction_disorder_of_the_heart|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome": 1,
    "Meniere_disease|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Cardiac_arrest|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|ANK2-related_disorder|not_specified|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Cardiac_arrest|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 2,
    "not_specified|Long_QT_syndrome|ANK2-related_disorder|Cardiovascular_phenotype": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "Cardiomyopathy|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome": 1,
    "not_provided|Acromesomelic_dysplasia_2B|Oligosynaptic_infertility|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "ANK2-associated_Complex_Neurodevelopmental_Disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|ANK2-associated_Complex_Neurodevelopmental_Disorder|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|ANK2-related_disorder|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|See_cases|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Meniere_disease|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|See_cases|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|ANK2-related_Autism": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|ANK2-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|ANK2-related_disorder|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_provided|Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Intellectual_disability|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Cardiomyopathy|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|not_provided": 2,
    "not_provided|See_cases|Cardiovascular_phenotype|Long_QT_syndrome|Sudden_cardiac_arrest": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Sudden_cardiac_death|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Conduction_disorder_of_the_heart": 1,
    "not_provided|ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|ANK2-related_disorder|not_provided": 1,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|ANK2-related_Autism|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Cardiovascular_phenotype": 2,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|Intellectual_disability|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Atrial_fibrillation|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_specified": 1,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 1,
    "ANK2-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Long_QT_syndrome_1": 8,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided|ANK2-related_disorder|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Long_QT_syndrome|Cardiovascular_phenotype|ANK2-related_disorder": 1,
    "not_provided|not_specified|Long_QT_syndrome": 6,
    "not_provided|Congestive_heart_failure": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Congenital_long_QT_syndrome|not_provided": 1,
    "ANK2-associated_Neurodevelopmental_Disorder": 3,
    "Meniere_disease|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Congenital_long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Intellectual_disability": 1,
    "not_provided|Long_QT_syndrome|not_specified|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome": 52,
    "Familial_dilated_cardiomyopathy_and_peripheral_neuropathy|ANK2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|ANK2-related_disorder": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|ANK2-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Congenital_long_QT_syndrome|ANK2-related_disorder": 1,
    "Long_QT_syndrome|Intellectual_disability|Cardiovascular_phenotype": 1,
    "ANK2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related|Supraventricular_tachycardia": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|Cardiomyopathy": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Ventricular_tachycardia|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|Long_QT_syndrome|not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder|not_provided|Cardiovascular_phenotype|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "not_provided|not_specified|ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|_ankyrin-B-related|ANK2-related_disorder": 1,
    "Long_QT_syndrome|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|not_provided|ANK2-related_disorder|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|ANK2-related_disorder|not_specified|Long_QT_syndrome|not_provided|Cardiomyopathy|Long_QT_syndrome_4|Cardiac_arrhythmia|_ankyrin-B-related|Death_in_infancy": 1,
    "not_provided|ANK2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|_ankyrin-B-related|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|ANK2-related_disorder|not_provided|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|ANK2-related_disorder|Ventricular_fibrillation|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|Long_QT_syndrome|Brugada_syndrome": 1,
    "not_provided|ANK2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|_ankyrin-B-related": 1,
    "not_provided|Cardiac_arrhythmia|_ankyrin-B-related|not_specified": 1,
    "Neurodevelopmental_disorder|CAMK2D-related_condition": 1,
    "CAMK2D-associated_neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_1": 74,
    "not_provided|Intellectual_disability|_autosomal_recessive_1": 8,
    "Intellectual_disability|_autosomal_recessive_1|not_provided": 5,
    "Intellectual_Disability|_Recessive": 26,
    "Intellectual_Disability|_Recessive|not_specified|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_recessive_1": 1,
    "Intellectual_disability|_autosomal_recessive_1|not_specified": 7,
    "not_specified|Intellectual_disability|_autosomal_recessive_1": 7,
    "not_specified|not_provided|Intellectual_Disability|_Recessive": 2,
    "PRSS12-related_disorder|not_provided|Intellectual_disability|_autosomal_recessive_1": 1,
    "PRSS12-related_disorder": 4,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_1": 4,
    "PRSS12-related_disorder|Intellectual_disability|_autosomal_recessive_1|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_1|PRSS12-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_1|not_provided|PRSS12-related_disorder": 1,
    "PRSS12-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_1": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_1|not_provided": 2,
    "SEC24D-related_disorder": 4,
    "Cole-Carpenter_syndrome_2|not_provided": 7,
    "not_provided|SEC24D-related_disorder": 4,
    "not_provided|Cole-Carpenter_syndrome_2": 9,
    "Cole-Carpenter_syndrome_2": 16,
    "SEC24D-related_disorder|Inborn_genetic_diseases|not_provided|Cole-Carpenter_syndrome_2": 1,
    "SEC24D-related_disorder|not_provided": 3,
    "SEC24D-related_disorder|Cole-Carpenter_syndrome_2|not_provided": 2,
    "Cole-Carpenter_syndrome_2|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|SEC24D-related_disorder": 1,
    "Cole-Carpenter_syndrome_2|Intellectual_disability|Seizure": 1,
    "not_provided|Cole-Carpenter_syndrome_2|not_specified": 1,
    "SEC24D-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Cole-Carpenter_syndrome_2|not_provided|SEC24D-related_disorder": 1,
    "Inborn_genetic_diseases|SEC24D-related_disorder": 1,
    "not_provided|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_16|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_16": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_16|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 11,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_16": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_16": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_16": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_16|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 14,
    "not_provided|MYOZ2-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_16|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_16|not_specified|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_16": 4,
    "not_provided|Hypertrophic_cardiomyopathy_16|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYOZ2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_16|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|MYOZ2-related_disorder": 1,
    "MYOZ2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 1,
    "MYOZ2-related_disorder|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_16|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 11,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_16": 2,
    "MYOZ2-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 8,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_16": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_16|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_16|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Restrictive_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_16|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 22,
    "not_provided|Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_16|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|MYOZ2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_16": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy": 10,
    "Hypertrophic_cardiomyopathy_16|Hypertrophic_cardiomyopathy": 2,
    "Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss": 24,
    "Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss|USP53-related_disorder": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss|Cholestasis": 5,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss": 2,
    "Cholestasis": 4,
    "Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss|Inborn_genetic_diseases": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_(PFIC4-like)|Cholestasis|not_provided|Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss": 1,
    "USP53-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss": 1,
    "See_cases|not_provided|Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss": 1,
    "Inborn_genetic_diseases|USP53-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_7|_with_or_without_hearing_loss": 1,
    "not_provided|FABP2_POLYMORPHISM": 1,
    "Brittle_cornea_syndrome_1": 97,
    "not_provided|Brittle_cornea_syndrome_1": 16,
    "PRDM5-related_disorder": 2,
    "Brittle_cornea_syndrome_2": 20,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome": 26,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 28,
    "Brittle_cornea_syndrome_2|not_provided": 8,
    "not_provided|not_specified|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 1,
    "not_provided|PRDM5-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 10,
    "not_specified|PRDM5-related_disorder|Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided": 18,
    "not_provided|Brittle_cornea_syndrome_2": 7,
    "not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_2": 3,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_provided": 24,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Brittle_cornea_syndrome_2": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_2": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 4,
    "Brittle_cornea_syndrome_2|Cardiovascular_phenotype": 1,
    "not_provided|PRDM5-related_disorder": 2,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|PRDM5-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 3,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 17,
    "not_provided|PRDM5-related_disorder|Ehlers-Danlos_syndrome": 1,
    "Brittle_cornea_syndrome_2|not_provided|not_specified": 1,
    "PRDM5-related_disorder|Cardiovascular_phenotype": 1,
    "Brittle_cornea_syndrome_2|Ehlers-Danlos_syndrome|not_provided": 1,
    "PRDM5-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_2|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_2": 3,
    "PRDM5-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Brittle_cornea_syndrome_2": 1,
    "PRDM5-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_2|PRDM5-related_disorder|not_provided": 1,
    "PRDM5-related_disorder|not_provided|Brittle_cornea_syndrome_2": 1,
    "Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 10,
    "not_provided|PRDM5-related_disorder|Brittle_cornea_syndrome_1|Connective_tissue_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|not_specified": 1,
    "not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 10,
    "not_provided|not_specified|Brittle_cornea_syndrome_2": 1,
    "Brittle_cornea_syndrome_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_2|not_provided": 1,
    "not_specified|not_provided|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_2": 1,
    "Hypogonadotropic_hypogonadism_25_with_anosmia|not_provided": 1,
    "Hypogonadotropic_hypogonadism_25_with_anosmia": 6,
    "not_provided|Hypogonadotropic_hypogonadism_25_with_anosmia": 5,
    "not_specified|Hypogonadotropic_hypogonadism_25_with_anosmia": 1,
    "Hypogonadotropic_hypogonadism_25_with_anosmia|not_specified": 1,
    "NDNF-related_condition": 1,
    "ANXA5-related_disorder": 2,
    "Pregnancy_loss|_recurrent|_susceptibility_to|_3": 3,
    "Pontocerebellar_hypoplasia|_type_1D|not_provided|Pontoneocerebellar_hypoplasia|Cerebral_atrophy": 1,
    "Pontocerebellar_hypoplasia|_type_1D": 6,
    "EXOSC9-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia|_type_1D": 2,
    "not_provided|Pontocerebellar_hypoplasia|_type_1D": 2,
    "not_provided|Inborn_genetic_diseases|Pontocerebellar_atrophy": 1,
    "not_provided|EXOSC9-related_disorder": 3,
    "not_provided|EXOSC9-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_7": 101,
    "not_provided|Bardet-Biedl_syndrome_7": 6,
    "BBS7-related_disorder|Bardet-Biedl_syndrome": 18,
    "BBS7-related_disorder|Bardet-Biedl_syndrome_7": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 21,
    "BBS7-related_disorder|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 8,
    "Bardet-Biedl_syndrome_7|BBS7-related_disorder": 5,
    "BBS7-related_disorder": 37,
    "Bardet-Biedl_syndrome_7|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|BBS7-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|BBS7-related_disorder": 3,
    "Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 36,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS7-related_disorder|Bardet-Biedl_syndrome_7": 1,
    "Bardet-Biedl_syndrome|BBS7-related_disorder|Bardet-Biedl_syndrome_7": 4,
    "BBS7-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|Optic_atrophy": 1,
    "Bardet-Biedl_syndrome_1|not_specified|Bardet-Biedl_syndrome_7|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|not_provided|Bardet-Biedl_syndrome|not_specified": 1,
    "Bardet-Biedl_syndrome|BBS7-related_disorder": 9,
    "not_provided|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_7|BBS7-related_disorder|Bardet-Biedl_syndrome": 5,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "BBS7-related_disorder|not_specified|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_7|Retinal_dystrophy": 3,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_7": 3,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_7": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|Inborn_genetic_diseases": 3,
    "not_specified|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_1|not_provided|not_specified|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "BBS7-related_disorder|Bardet-Biedl_syndrome_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome|BBS7-related_ciliopathy|BBS7-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|BBS7-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_7|Inborn_genetic_diseases": 2,
    "BBS7-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 4,
    "BBS7-related_disorder|Bardet-Biedl_syndrome|not_specified": 1,
    "BBS7-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 2,
    "not_provided|Bardet-Biedl_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_7|BBS7-related_ciliopathy": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "BBS7-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS7-related_ciliopathy": 1,
    "not_provided|BBS7-related_disorder|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome|not_specified": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|Retinal_dystrophy": 1,
    "BBS7-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 1,
    "Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome|BBS7-related_disorder|Inborn_genetic_diseases": 1,
    "BBS7-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_specified|not_provided|BBS7-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|BBS7-related_disorder": 1,
    "BBS7-related_disorder|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Bardet-Biedl_syndrome_7|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 2,
    "not_specified|not_provided|Bardet-Biedl_syndrome_7": 1,
    "BBS7-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_7": 1,
    "BBS7-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|not_specified": 1,
    "BBS7-related_ciliopathy": 1,
    "BBS7-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_7|not_provided": 1,
    "Bardet-Biedl_syndrome_7|BBS7-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1/7|_digenic": 1,
    "Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome|BBS7-related_disorder": 4,
    "Retinal_dystrophy|Bardet-Biedl_syndrome": 8,
    "Inborn_genetic_diseases|BBS7-related_disorder": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS7-related_disorder": 1,
    "See_cases|Bardet-Biedl_syndrome_7|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_7": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7|BBS7-related_disorder": 1,
    "Bardet-Biedl_syndrome|not_provided|not_specified|Bardet-Biedl_syndrome_7": 1,
    "not_specified|not_provided|BBS7-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 1,
    "BBS7-related_disorder|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_7|not_provided|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS7-related_disorder|Bardet-Biedl_syndrome_7": 1,
    "not_provided|BBS7-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|not_specified|Bardet-Biedl_syndrome|not_provided": 1,
    "BBS7-related_ciliopathy|BBS7-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_7": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 63,
    "Bardet-Biedl_syndrome_7|Optic_atrophy|Bardet-Biedl_syndrome|BBS7-related_disorder": 1,
    "Spinocerebellar_ataxia_type_41": 6,
    "not_provided|TRPC3-related_disorder": 7,
    "not_provided|Spinocerebellar_ataxia_type_41": 2,
    "TRPC3-related_disorder|not_provided": 2,
    "Spinocerebellar_ataxia_type_41|not_provided": 1,
    "TRPC3-related_disorder": 3,
    "not_specified|TRPC3-related_disorder": 1,
    "BLTP1-related_disorder": 45,
    "not_provided|Alkuraya-Kucinskas_syndrome": 5,
    "BLTP1-related_disorder|not_provided": 3,
    "Alkuraya-Kucinskas_syndrome": 61,
    "BLTP1-related_disorder|Alkuraya-Kucinskas_syndrome|not_provided": 1,
    "Clubfoot|Arthrogryposis_multiplex_congenita|Severe_hydrocephalus": 2,
    "Alkuraya-Kucinskas_syndrome|Dandy-Walker_syndrome|Clubfoot|Hydrocephalus|Flexed_deformity|Pleural_effusion|Micrognathia": 1,
    "not_provided|BLTP1-related_disorder": 21,
    "not_specified|Alkuraya-Kucinskas_syndrome": 8,
    "not_specified|Alkuraya-Kucinskas_syndrome|not_provided": 2,
    "Alkuraya-Kucinskas_syndrome|not_specified": 4,
    "Alkuraya-Kucinskas_syndrome|not_provided": 3,
    "not_specified|not_provided|Alkuraya-Kucinskas_syndrome": 1,
    "not_specified|BLTP1-related_disorder|Alkuraya-Kucinskas_syndrome|not_provided": 1,
    "not_specified|BLTP1-related_disorder": 3,
    "Right_aortic_arch|Hemivertebrae|Renal_agenesis": 2,
    "BLTP1-related_disorder|not_specified": 3,
    "BLTP1-related_disorder|not_specified|Alkuraya-Kucinskas_syndrome": 1,
    "not_provided|BLTP1-related_disorder|not_specified": 1,
    "BLTP1-related_disorder|not_specified|not_provided": 1,
    "IL2-related_disorder": 1,
    "IL21-related_disorder": 1,
    "IL21-related_infantile_inflammatory_bowel_disease|not_provided|not_specified": 1,
    "IL21-related_infantile_inflammatory_bowel_disease": 1,
    "IL21-related_infantile_inflammatory_bowel_disease|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_12": 131,
    "Bardet-Biedl_syndrome_12|not_provided": 6,
    "BBS12-related_disorder": 36,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS12-related_disorder|Bardet-Biedl_syndrome_12|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 53,
    "Bardet-Biedl_syndrome|BBS12-related_disorder": 12,
    "Bardet-Biedl_syndrome_12|BBS12-related_disorder|Bardet-Biedl_syndrome": 6,
    "BBS12-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 3,
    "not_provided|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_12": 1,
    "BBS12-related_disorder|Bardet-Biedl_syndrome": 20,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 3,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS12-related_disorder|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|BBS12-related_disorder": 5,
    "Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 33,
    "BBS12-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 6,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|not_provided": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 2,
    "not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_12": 1,
    "BBS12-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|BBS12-related_disorder": 6,
    "BBS12-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "BBS12-related_disorder|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 5,
    "not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Abnormality_of_the_nervous_system|BBS12-related_disorder": 1,
    "Bardet-Biedl_syndrome|BBS12-related_disorder|Bardet-Biedl_syndrome_12|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_12|BBS12-related_disorder": 6,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome|not_specified|not_provided|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome|Retinal_dystrophy|BBS12-related_disorder|Bardet-Biedl_syndrome_12": 1,
    "BBS12-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Retinal_dystrophy": 2,
    "BBS12-related_ciliopathy": 1,
    "not_provided|Bardet-Biedl_syndrome|BBS12-related_disorder|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|Retinal_dystrophy|not_provided|BBS12-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|BBS12-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|BBS12-related_disorder": 1,
    "not_provided|BBS12-related_disorder|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|BBS12-related_disorder": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|BBS12-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome_12|not_specified": 1,
    "Retinal_dystrophy|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_1|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|not_provided": 1,
    "Inability_to_walk|Visual_impairment|Abnormal_cardiovascular_system_morphology|Polydactyly|_postaxial|_type_A1|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_12": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|not_specified|not_provided|Bardet-Biedl_syndrome": 1,
    "BBS12-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "BBS12-related_ciliopathy|BBS12-related_disorder|Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_12|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_12|BBS12-related_disorder|not_specified|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_12": 2,
    "not_provided|Bardet-Biedl_syndrome_12|BBS12-related_disorder|Bardet-Biedl_syndrome": 2,
    "not_provided|Bardet-Biedl_syndrome|BBS12-related_disorder|not_specified|Bardet-Biedl_syndrome_12": 1,
    "not_specified|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|not_provided|BBS12-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|not_specified|not_provided|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome|BBS12-related_disorder|Bardet-Biedl_syndrome_12|Retinal_dystrophy|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_12": 1,
    "Inborn_genetic_diseases|BBS12-related_disorder|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_12|BBS12-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Retinitis_pigmentosa": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|not_specified|BBS12-related_disorder": 1,
    "Bardet-Biedl_syndrome|BBS12-related_disorder|Bardet-Biedl_syndrome_12": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_12": 1,
    "BBS12-related_disorder|Bardet-Biedl_syndrome_12": 3,
    "BBS12-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_12|not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_12|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|not_specified|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_12|not_provided": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_12|BBS12-related_disorder": 2,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS12-related_disorder|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS12-related_disorder": 2,
    "BBS12-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|BBS12-related_ciliopathy|not_provided|BBS12-related_disorder|Bardet-Biedl_syndrome_12": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12|BBS12-related_disorder|Retinal_dystrophy": 1,
    "not_provided|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|Inborn_genetic_diseases|not_provided|BBS12-related_disorder": 1,
    "Bardet-Biedl_syndrome_12|BBS12-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_12|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome|BBS12-related_disorder": 1,
    "BBS12-related_disorder|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|BBS12-related_disorder|Bardet-Biedl_syndrome": 1,
    "BBS12-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_1": 1,
    "BBS12-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "BBS12-related_disorder|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_12|BBS12-related_ciliopathy|Bardet-Biedl_syndrome_1|not_specified": 1,
    "Retinal_dystrophy|BBS12-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|BBS12-related_disorder": 1,
    "BBS12-related_disorder|not_provided|Bardet-Biedl_syndrome_12": 1,
    "not_provided|BBS12-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_12": 1,
    "Bardet-Biedl_syndrome_12|Bardet-Biedl_syndrome|not_provided": 2,
    "Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|Retinal_dystrophy|BBS12-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome_12|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "NUDT6-related_disorder": 5,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_specified|not_provided": 2,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 602,
    "not_provided|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_provided": 7,
    "Inborn_genetic_diseases|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 19,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|Inborn_genetic_diseases": 9,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_provided": 31,
    "not_provided|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 32,
    "not_provided|Neurodevelopmental_disorder|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 1,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "AFG2A-related_disorder": 2,
    "AFG2A-related_disorder|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|AFG2A-related_disorder|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 1,
    "AFG2A-related_disorder|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_provided": 2,
    "not_specified|not_provided|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 2,
    "not_specified|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 2,
    "not_provided|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|AFG2A-related_disorder": 1,
    "not_specified|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 2,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|AFG2A-related_disorder": 1,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|Syndromic_complex_neurodevelopmental_disorder": 1,
    "AFG2A-related_disorder|not_provided|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 2,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_specified": 1,
    "not_specified|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|SPATA5-related_disorder|SPATA5-related_neurodevelopmental_disorder|not_provided": 1,
    "not_provided|not_specified|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|Syndromic_complex_neurodevelopmental_disorder": 1,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|AFG2A-related_disorder|not_provided": 1,
    "Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 1,
    "not_provided|AFG2A-related_disorder|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 1,
    "Syndromic_complex_neurodevelopmental_disorder|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 1,
    "not_provided|not_specified|Microcephaly-intellectual_disability-sensorineural_hearing_loss-epilepsy-abnormal_muscle_tone_syndrome": 1,
    "SPRY1-related_disorder": 5,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 250,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided": 41,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 6,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 30,
    "FAT4-related_disorder|not_provided": 39,
    "not_provided|FAT4-related_disorder": 32,
    "not_provided|Anophthalmia-microphthalmia_syndrome|Irido-corneo-trabecular_dysgenesis": 1,
    "not_provided|Intellectual_disability|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided": 6,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided|FAT4-related_disorder": 1,
    "Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 8,
    "not_provided|FAT4-related_disorder|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 2,
    "FAT4-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 56,
    "not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Inborn_genetic_diseases": 7,
    "not_specified|not_provided|Lymphedema": 1,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|Inborn_genetic_diseases": 7,
    "not_provided|Inborn_genetic_diseases|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 7,
    "not_provided|FAT4-related_disorder|not_specified": 5,
    "Inborn_genetic_diseases|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 8,
    "FAT4-related_disorder|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|Inborn_genetic_diseases": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1": 154,
    "FAT4-related_disorder": 21,
    "Microcephaly|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "FAT4-related_disorder|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_specified|not_provided": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2": 21,
    "not_provided|Van_Maldergem_syndrome_2|Inborn_genetic_diseases": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 44,
    "not_specified|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 2,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 4,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided|Inborn_genetic_diseases": 4,
    "FAT4-related_disorder|not_specified|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|FAT4-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|FAT4-related_disorder": 5,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability": 15,
    "Inborn_genetic_diseases|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 3,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Inborn_genetic_diseases|not_provided": 5,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided": 1,
    "FAT4-related_disorder|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided": 2,
    "Van_Maldergem_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|FAT4-related_disorder|not_provided": 2,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_specified": 4,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|Inborn_genetic_diseases": 10,
    "not_provided|Van_Maldergem_syndrome_2": 4,
    "not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|FAT4-related_disorder": 2,
    "not_specified|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 2,
    "Inborn_genetic_diseases|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 10,
    "not_specified|not_provided|FAT4-related_disorder": 7,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 6,
    "not_provided|not_specified|FAT4-related_disorder": 3,
    "FAT4-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_specified": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|FAT4-related_disorder|not_provided": 3,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|FAT4-related_disorder": 1,
    "not_specified|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 1,
    "Van_Maldergem_syndrome_2|not_provided": 3,
    "FAT4-related_disorder|not_specified|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 1,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 3,
    "Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 4,
    "FAT4-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_specified|not_provided": 4,
    "not_provided|Van_Maldergem_syndrome": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_specified|Van_Maldergem_syndrome_2|not_provided": 1,
    "not_specified|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "Inborn_genetic_diseases|not_provided|FAT4-related_disorder|not_specified": 2,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|FAT4-related_disorder|not_provided": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_specified|not_provided|Van_Maldergem_syndrome_2": 1,
    "FAT4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 2,
    "not_specified|FAT4-related_disorder|not_provided|Intellectual_disability": 1,
    "FAT4-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "FAT4-related_disorder|Inborn_genetic_diseases": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "FAT4-related_disorder|Van_Maldergem_syndrome_2|not_provided": 1,
    "FAT4-related_disorder|not_specified|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "FAT4-related_disorder|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_provided": 1,
    "FAT4-related_disorder|Inborn_genetic_diseases|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Van_Maldergem_syndrome_1|Hennekam_lymphangiectasia-lymphedema_syndrome_1|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "FAT4-related_disorder|Capillary_infantile_hemangioma|not_provided": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|See_cases": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "Congenital_chromosomal_disease|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_specified|not_provided": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_specified": 1,
    "Van_Maldergem_syndrome_1|Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 3,
    "Inborn_genetic_diseases|not_provided|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_specified": 1,
    "not_provided|Intellectual_disability|FAT4-related_disorder|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2": 1,
    "Lymphedema": 2,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|not_specified|Van_Maldergem_syndrome_2": 1,
    "FAT4-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_2|Inborn_genetic_diseases": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided|not_specified": 1,
    "not_provided|FAT4-related_disorder|Inborn_genetic_diseases": 1,
    "Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_2|Van_Maldergem_syndrome_2|not_provided|Congenital_chromosomal_disease": 1,
    "not_provided|not_specified|Van_Maldergem_syndrome_2|Hennekam_lymphangiectasia-lymphedema_syndrome_2": 1,
    "not_specified|FAT4-related_disorder|not_provided": 1,
    "INTU-related_disorder|not_provided": 11,
    "Orofaciodigital_syndrome_17|Mohr_syndrome": 1,
    "not_provided|INTU-related_disorder|Orofaciodigital_syndrome_17|Short-rib_thoracic_dysplasia_20_with_polydactyly": 1,
    "Orofaciodigital_syndrome_17": 2,
    "Short-rib_thoracic_dysplasia_20_with_polydactyly|Orofaciodigital_syndrome_17|not_provided": 2,
    "not_provided|Short-rib_thoracic_dysplasia_20_with_polydactyly|Orofaciodigital_syndrome_17|INTU-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_7/20_with_polydactyly|_digenic|Short-rib_thoracic_dysplasia_20_with_polydactyly|not_provided": 1,
    "Short_rib-polydactyly_syndrome|Short-rib_thoracic_dysplasia_20_with_polydactyly": 1,
    "INTU-related_disorder": 4,
    "Short-rib_thoracic_dysplasia_20_with_polydactyly|Orofaciodigital_syndrome_17": 2,
    "not_specified|INTU-related_disorder|Growth_delay|Nephronophthisis|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_20_with_polydactyly|Orofaciodigital_syndrome_17": 1,
    "Short-rib_thoracic_dysplasia_20_with_polydactyly|Short_rib-polydactyly_syndrome": 1,
    "INTU-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|INTU-related_disorder|not_provided": 1,
    "not_specified|INTU-related_disorder|not_provided": 1,
    "not_provided|PLK4-related_disorder": 4,
    "PLK4-related_microcephaly_and_growth_failure_with_or_without_ocular_features": 2,
    "not_provided|Microcephaly_and_chorioretinopathy_2": 4,
    "Microcephaly_and_chorioretinopathy_2": 4,
    "Microcephaly_and_chorioretinopathy_2|not_provided": 6,
    "not_provided|PLK4-related_disorder|not_specified": 1,
    "Microcephaly_and_chorioretinopathy_2|not_provided|PLK4-related_disorder": 1,
    "PLK4-related_disorder|not_provided": 6,
    "PLK4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PLK4-related_disorder": 2,
    "Neuronal_ceroid_lipofuscinosis_7": 599,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided": 20,
    "Late-infantile_neuronal_ceroid_lipofuscinosis": 26,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 3,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_7": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_7": 10,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases|not_provided": 2,
    "Cone-rod_dystrophy|Retinal_dystrophy": 2,
    "Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis": 16,
    "Inborn_genetic_diseases|Macular_dystrophy_with_central_cone_involvement|Neuronal_ceroid_lipofuscinosis_7|not_provided": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_7": 28,
    "Macular_dystrophy_with_central_cone_involvement|Neuronal_ceroid_lipofuscinosis_7": 12,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7|not_provided": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 3,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_7": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 26,
    "Macular_dystrophy_with_central_cone_involvement|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases|Retinitis_pigmentosa|Neuronal_ceroid_lipofuscinosis|Retinal_dystrophy|not_provided|Cone-rod_dystrophy|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Abnormality_of_the_nervous_system": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided": 5,
    "Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|not_provided|not_specified|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_7|Retinal_dystrophy|MFSD8-related_disorder|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 3,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|MF5D8-related_disorder|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases|MFSD8-related_disorder|not_specified": 1,
    "Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|not_specified|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases|not_provided|Macular_dystrophy_with_central_cone_involvement|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7": 8,
    "Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases|not_provided|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_7": 2,
    "Inborn_genetic_diseases|Macular_dystrophy_with_central_cone_involvement|Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|Late-infantile_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement": 5,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided|Macular_dystrophy_with_central_cone_involvement|Late-infantile_neuronal_ceroid_lipofuscinosis": 3,
    "Neuronal_ceroid_lipofuscinosis_7|not_specified": 4,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided|Late-infantile_neuronal_ceroid_lipofuscinosis": 2,
    "Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis": 2,
    "Neuronal_ceroid_lipofuscinosis_7|Retinal_dystrophy": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|not_specified": 1,
    "MFSD8-related_disorder|Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|Macular_dystrophy_with_central_cone_involvement|Retinal_dystrophy|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_7|Optic_atrophy": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "MFSD8-related_disorder|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Inborn_genetic_diseases|not_provided|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_7": 2,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 4,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided|Macular_dystrophy_with_central_cone_involvement": 3,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_7|MFSD8-related_disorder": 1,
    "Macular_dystrophy_with_central_cone_involvement": 3,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|Inborn_genetic_diseases": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_7|Retinal_dystrophy": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7": 1,
    "MFSD8-related_disorder|not_specified|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Inborn_genetic_diseases|Hereditary_ataxia|Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis_7": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement": 1,
    "not_provided|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 2,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_7|Retinal_dystrophy": 1,
    "Microcephaly_5|_primary|_autosomal_recessive|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_7|MFSD8-related_disorder|not_specified|Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Inborn_genetic_diseases|MFSD8-related_disorder|not_specified|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement": 1,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement": 1,
    "Inborn_genetic_diseases|MFSD8-related_disorder|not_provided|Neuronal_ceroid_lipofuscinosis_7": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided|Inborn_genetic_diseases|Macular_dystrophy_with_central_cone_involvement|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis|not_specified|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|not_specified|not_provided": 1,
    "not_provided|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|Inborn_genetic_diseases": 1,
    "Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_7|not_provided|Late-infantile_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Macular_dystrophy_with_central_cone_involvement|Inborn_genetic_diseases|Late-infantile_neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_7|Late-infantile_neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Retinal_dystrophy|Late-infantile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_7": 1,
    "Hypermetropia|Astigmatism|Hamartoma_of_hypothalamus|Global_developmental_delay|Nystagmus|Opsoclonus": 2,
    "SCLT1-related_disorder|not_provided": 17,
    "SCLT1-related_disorder": 18,
    "SCLT1-related_disorder|not_provided|not_specified": 4,
    "not_provided|not_specified|SCLT1-related_disorder": 3,
    "SCLT1-related_disorder|not_specified|not_provided": 5,
    "not_provided|SCLT1-related_disorder": 9,
    "Esophageal_atresia/tracheoesophageal_fistula|not_provided|SCLT1-related_disorder": 1,
    "not_provided|SCLT1-related_disorder|not_specified": 1,
    "Orofaciodigital_syndrome_IX": 4,
    "SCLT1-related_disorder|not_specified": 1,
    "not_specified|not_provided|SCLT1-related_disorder": 2,
    "not_specified|SCLT1-related_disorder|not_provided": 2,
    "not_provided|Esophageal_atresia/tracheoesophageal_fistula|SCLT1-related_disorder": 1,
    "Retinal_dystrophy|Optic_atrophy|not_specified|SCLT1-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_50": 80,
    "Intellectual_disability|_autosomal_dominant_50|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NAA15-related_disorder": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_50|Inborn_genetic_diseases": 1,
    "NAA15-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_50|Global_developmental_delay|Intellectual_disability|See_cases": 1,
    "Intellectual_disability|_autosomal_dominant_50|not_provided": 8,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_50": 2,
    "NAA15-related_disorder|Incidental_Discovery": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_50": 2,
    "NAA15-related_disorder": 14,
    "Intellectual_disability|_autosomal_dominant_50|Neurodevelopmental_disorder|not_provided": 1,
    "NAA15-related_disorder|not_provided": 7,
    "not_provided|NAA15-related_disorder": 5,
    "NAA15-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_dominant_50": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_50": 8,
    "Intellectual_disability|_autosomal_dominant_50|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_50|Inborn_genetic_diseases": 1,
    "not_provided|intellectual_developmental_disorder-50_with_behavioral_abnormalities_(MRD50)": 1,
    "not_provided|NAA15-related_syndrome": 1,
    "NAA15-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_50|not_provided": 1,
    "Smith-McCort_dysplasia": 9,
    "Smith-McCort_dysplasia|not_provided": 2,
    "not_provided|Smith-McCort_dysplasia": 1,
    "not_provided|Smith-McCort_dysplasia_2": 8,
    "Smith-McCort_dysplasia_2": 55,
    "not_provided|Smith-McCort_dysplasia_2|Inborn_genetic_diseases": 1,
    "Smith-McCort_dysplasia_2|not_provided": 12,
    "Smith-McCort_dysplasia_2|See_cases": 1,
    "not_provided|RAB33B-related_disorder|Smith-McCort_dysplasia_2": 1,
    "Smith-McCort_dysplasia_2|Inborn_genetic_diseases": 1,
    "ELMOD2-related_disorder": 3,
    "UCP1_POLYMORPHISM": 1,
    "GAB1-related_disorder": 7,
    "not_specified|15q14_microdeletion_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_26": 2,
    "SMARCA5-related_disorder": 7,
    "SMARCA5-associated_neurodevelopmental_disorder": 3,
    "not_provided|Short_stature|Failure_to_thrive|Microcephaly|Pubertal_developmental_failure_in_females": 1,
    "not_provided|Pes_planus|Global_developmental_delay|Delayed_CNS_myelination|Hypotonia": 1,
    "BLOOD_GROUP|_Ss": 1,
    "BLOOD_GROUP_ERIK": 1,
    "Chronic_obstructive_pulmonary_disease|_biomass_related|Chronic_obstructive_pulmonary_disease": 3,
    "HHIP-related_condition": 1,
    "Mayer_Rokitansky_Kuster_Hauser_syndrome_type_1": 7,
    "not_provided|Amenorrhea": 4,
    "OTUD4-related_disorder": 4,
    "Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies": 17,
    "not_provided|OTUD4-related_disorder": 1,
    "Variant_of_unknown_significance|Pulmonary_hypertension|_primary|_1": 1,
    "SMAD1-related_disorder": 1,
    "not_specified|Methylmalonic_aciduria|_cblA_type": 3,
    "Methylmalonic_aciduria|_cblA_type": 476,
    "not_provided|not_specified|Methylmalonic_aciduria|_cblA_type": 1,
    "not_provided|Methylmalonic_aciduria|_cblA_type": 13,
    "MMAA-related_disorder|Methylmalonic_aciduria|_cblA_type": 3,
    "Inborn_genetic_diseases|Methylmalonic_aciduria|_cblA_type": 15,
    "Methylmalonic_aciduria|_cblA_type|MMAA-related_disorder": 4,
    "not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type": 2,
    "Methylmalonic_aciduria|_cblA_type|Methylmalonic_aciduria_of_the_cblA_complementation_type": 1,
    "Methylmalonic_aciduria|_cblA_type|not_provided|not_specified": 1,
    "Methylmalonic_aciduria|_cblA_type|Inborn_genetic_diseases": 10,
    "Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type": 4,
    "Methylmalonic_aciduria|_cblA_type|Microcephaly|Cataract|Severe_global_developmental_delay|not_provided": 1,
    "Methylmalonic_aciduria|_cblB_type": 407,
    "Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type|MMAA-related_disorder|not_provided": 1,
    "Methylmalonic_aciduria|_cblA_type|Methylmalonic_acidemia": 4,
    "MMAA-related_disorder|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type|See_cases": 1,
    "Methylmalonic_aciduria|_cblA_type|not_provided|Methylmalonic_acidemia": 1,
    "Methylmalonic_aciduria|_cblA_type|Methylmalonic_acidemia|not_provided": 1,
    "MMAA-related_disorder|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type": 1,
    "MMAA-related_disorder|not_specified|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type|not_provided": 1,
    "not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type|not_specified": 1,
    "Methylmalonic_aciduria|_cblA_type|not_provided": 15,
    "not_provided|Methylmalonic_aciduria|_cblA_type|Inborn_genetic_diseases": 1,
    "Methylmalonic_aciduria|_cblA_type|not_specified|MMAA-related_disorder": 1,
    "not_specified|Methylmalonic_aciduria|_cblA_type|not_provided": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblA_type": 1,
    "MMAA-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Methylmalonic_aciduria|_cblA_type": 1,
    "Methylmalonic_aciduria|_cblA_type|not_specified": 1,
    "not_specified|not_provided|Methylmalonic_aciduria|_cblA_type": 2,
    "See_cases|Methylmalonic_aciduria|_cblA_type": 1,
    "Inborn_genetic_diseases|not_provided|Methylmalonic_aciduria|_cblA_type": 1,
    "SLC10A7-related_disorder|not_provided": 5,
    "not_provided|Short_stature|_amelogenesis_imperfecta|_and_skeletal_dysplasia_with_scoliosis|Inborn_genetic_diseases": 1,
    "Short_stature|_amelogenesis_imperfecta|_and_skeletal_dysplasia_with_scoliosis": 6,
    "not_provided|SLC10A7-related_disorder": 1,
    "not_provided|Short_stature|_amelogenesis_imperfecta|_and_skeletal_dysplasia_with_scoliosis": 1,
    "Short_stature|_amelogenesis_imperfecta|_and_skeletal_dysplasia_with_scoliosis|not_provided": 1,
    "Spermatogenic_failure_42": 7,
    "TTC29-related_condition": 1,
    "Migraine|_resistance_to": 1,
    "not_provided|Migraine_with_or_without_aura|_susceptibility_to|_1|Mandibulofacial_dysostosis_with_alopecia": 1,
    "not_provided|Mandibulofacial_dysostosis_with_alopecia|Migraine_with_or_without_aura|_susceptibility_to|_1": 1,
    "Mandibulofacial_dysostosis_with_alopecia": 3,
    "EDNRA-related_disorder|Migraine_with_or_without_aura|_susceptibility_to|_1|Mandibulofacial_dysostosis_with_alopecia|not_provided": 1,
    "Migraine_with_or_without_aura|_susceptibility_to|_1|Mandibulofacial_dysostosis_with_alopecia": 1,
    "Migraine_with_or_without_aura|_susceptibility_to|_1|Mandibulofacial_dysostosis_with_alopecia|not_provided": 2,
    "EDNRA-related_disorder|not_provided": 1,
    "Mandibulofacial_dysostosis_with_alopecia|not_provided": 2,
    "Mandibulofacial_dysostosis_with_alopecia|Migraine_with_or_without_aura|_susceptibility_to|_1|not_provided": 1,
    "Migraine_with_or_without_aura|_susceptibility_to|_1|Mandibulofacial_dysostosis_with_alopecia|EDNRA-related_disorder|not_provided": 1,
    "Neurodevelopmental_abnormality|not_specified": 1,
    "not_specified|Neurodevelopmental_abnormality": 2,
    "Meckel_syndrome|_type_9": 7,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Pseudohyperaldosteronism_type_2|Autosomal_dominant_pseudohypoaldosteronism_type_1": 59,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohyperaldosteronism_type_2": 4,
    "Pseudohyperaldosteronism_type_2|Autosomal_dominant_pseudohypoaldosteronism_type_1|Inborn_genetic_diseases": 6,
    "Pseudohyperaldosteronism_type_2": 1,
    "NR3C2-related_disorder|Autosomal_dominant_pseudohypoaldosteronism_type_1|Inborn_genetic_diseases": 1,
    "NR3C2-related_disorder|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "Renal_tubulopathies": 1,
    "NR3C2-related_disorder": 8,
    "NR3C2-related_disorder|Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohyperaldosteronism_type_2|Hypertension|_early-onset|_autosomal_dominant|_with_exacerbation_in_pregnancy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohyperaldosteronism_type_2": 6,
    "Inborn_genetic_diseases|Pseudohyperaldosteronism_type_2|Autosomal_dominant_pseudohypoaldosteronism_type_1": 2,
    "not_specified|not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "not_specified|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 1,
    "Pseudohyperaldosteronism_type_2|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 9,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohyperaldosteronism_type_2|not_provided": 2,
    "not_provided|Pseudohyperaldosteronism_type_2|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided|NR3C2-related_disorder|Inborn_genetic_diseases|Pseudohyperaldosteronism_type_2": 1,
    "not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_specified": 3,
    "Autism_spectrum_disorder|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "Pseudohypoaldosteronism": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_pseudohypoaldosteronism_type_1": 3,
    "NR3C2-related_disorder|not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1|NR3C2-related_disorder": 1,
    "not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1|Pseudohyperaldosteronism_type_2": 1,
    "NR3C2-related_disorder|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_provided": 1,
    "Pseudohyperaldosteronism_type_2|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "not_provided|NR3C2-related_disorder": 1,
    "Autosomal_dominant_pseudohypoaldosteronism_type_1|not_specified|not_provided": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|Inborn_genetic_diseases": 58,
    "not_specified|LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency": 1569,
    "LRBA-related_disorder": 5,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided": 34,
    "LRBA-related_disorder|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_LRBA_deficiency": 2,
    "not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|Inborn_genetic_diseases": 10,
    "not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency|Inborn_genetic_diseases": 1,
    "LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency": 17,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|See_cases": 2,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_LRBA_deficiency": 94,
    "not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 58,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA-related_disorder": 15,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided|not_specified": 5,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided|Inborn_genetic_diseases|LRBA-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA-related_disorder": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 6,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided": 2,
    "LRBA_deficiency": 2,
    "LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 10,
    "not_provided|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_LRBA_deficiency": 4,
    "not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency": 7,
    "LRBA-related_disorder|not_provided|not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA-related_disorder|not_specified": 1,
    "not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided": 8,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|not_specified": 6,
    "LRBA-related_disorder|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 3,
    "not_provided|not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency": 3,
    "LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "Colobomatous_microphthalmia-rhizomelic_dysplasia_syndrome": 12,
    "not_provided|MAB21L2-related_disorder": 1,
    "MAB21L2-related_disorder": 1,
    "Colobomatous_microphthalmia-rhizomelic_dysplasia_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|not_specified|not_provided": 4,
    "not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|See_cases": 1,
    "Inborn_genetic_diseases|LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency": 2,
    "not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA-related_disorder|Inborn_genetic_diseases": 1,
    "LRBA-related_disorder|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|not_specified": 1,
    "not_provided|LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency": 2,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|Inherited_Immunodeficiency_Diseases": 2,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA_deficiency": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity": 1,
    "not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "not_provided|not_specified|Combined_immunodeficiency_due_to_LRBA_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|LRBA-related_disorder|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "not_specified|LRBA-related_disorder|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 2,
    "not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|LRBA-related_disorder": 2,
    "LRBA-related_disorder|not_specified|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency": 2,
    "LRBA-related_disorder|not_specified|not_provided|Combined_immunodeficiency_due_to_LRBA_deficiency|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Meniere_disease|Combined_immunodeficiency_due_to_LRBA_deficiency": 1,
    "Combined_immunodeficiency_due_to_LRBA_deficiency|Meniere_disease": 1,
    "SH3D19-related_disorder": 9,
    "GATB-related_disorder": 9,
    "Combined_oxidative_phosphorylation_deficiency_41": 3,
    "not_provided|GATB-related_disorder": 4,
    "Combined_oxidative_phosphorylation_deficiency_41|not_specified|GATB-related_disorder|not_provided": 1,
    "GATB-related_disorder|not_specified": 1,
    "GATB-related_disorder|not_provided": 2,
    "Cardiomyopathy|_mitochondrial|Combined_oxidative_phosphorylation_deficiency_41": 2,
    "not_specified|GATB-related_disorder": 1,
    "GATB-related_disorder|Combined_oxidative_phosphorylation_deficiency_41|not_provided": 1,
    "Developmental_delay|_hypotonia|_and_impaired_language": 17,
    "Developmental_delay|_hypotonia|_and_impaired_language|not_provided": 2,
    "FBXW7-related_disorder|not_provided": 2,
    "not_provided|FBXW7-related_disorder": 3,
    "FBXW7-related_disorder|Inborn_genetic_diseases": 1,
    "FBXW7-related_disorder": 15,
    "Inborn_genetic_diseases|not_provided|FBXW7-related_disorder": 1,
    "FBXW7-related_neurodevelopmental_disorder": 1,
    "Pervasive_developmental_disorder|Developmental_delay|_hypotonia|_and_impaired_language": 1,
    "FBXW7-related_disorder|not_specified|not_provided": 2,
    "FBXW7-related_disorder|not_provided|not_specified": 1,
    "not_provided|Developmental_delay|_hypotonia|_and_impaired_language": 1,
    "Predisposition_to_Wilm's_tumor|_FBXW7-related": 1,
    "Developmental_delay|_hypotonia|_and_impaired_language|FBXW7-related_disorder": 1,
    "TRIM2-related_disorder": 2,
    "Charcot-Marie-Tooth_disease_type_2R": 389,
    "TRIM2-related_disorder|Charcot-Marie-Tooth_disease_type_2R": 3,
    "not_provided|TRIM2-related_disorder|Charcot-Marie-Tooth_disease_type_2R|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2R": 10,
    "Charcot-Marie-Tooth_disease_type_2R|not_provided": 13,
    "Charcot-Marie-Tooth_disease_type_2R|not_specified": 15,
    "not_specified|Charcot-Marie-Tooth_disease_type_2R": 10,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2R": 1,
    "Charcot-Marie-Tooth_disease_type_2R|not_provided|not_specified": 2,
    "not_specified|Charcot-Marie-Tooth_disease_type_2R|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_2R|not_specified|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_2R|TRIM2-related_disorder|not_provided": 1,
    "TLR2-related_disorder": 9,
    "TLR2-related_disorder|not_provided|Colorectal_cancer|Leprosy|_susceptibility_to|_3|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "TLR2-related_disorder|COVID-19\u2013associated_multisystem_inflammatory_syndrome_in_adults": 2,
    "not_provided|TLR2-related_disorder": 1,
    "Colorectal_cancer|Leprosy|_susceptibility_to|_3": 2,
    "Leprosy|_susceptibility_to|_3|Colorectal_cancer|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "TLR2-related_disorder|Mycobacterium_tuberculosis|_susceptibility_to|Colorectal_cancer|Leprosy|_susceptibility_to|_3|not_provided": 1,
    "TLR2-related_disorder|not_provided": 1,
    "Leprosy|_susceptibility_to|_3": 1,
    "not_specified|Anophthalmia-microphthalmia_syndrome": 2,
    "DCHS2-related_disorder": 104,
    "not_provided|DCHS2-related_disorder": 6,
    "Multiple_congenital_anomalies": 1,
    "DCHS2-related_disorder|not_provided": 3,
    "FIBRINOGEN-BETA_POLYMORPHISM": 1,
    "not_provided|FIBRINOGEN|_BETA-148_POLYMORPHISM": 1,
    "Congenital_afibrinogenemia": 95,
    "not_provided|Inborn_genetic_diseases|Congenital_afibrinogenemia": 1,
    "Congenital_afibrinogenemia|Inborn_genetic_diseases": 2,
    "FGB-related_disorder": 7,
    "not_specified|Congenital_afibrinogenemia|not_provided": 3,
    "not_provided|not_specified|Congenital_afibrinogenemia": 3,
    "FIBRINOGEN_CHRISTCHURCH_2|See_cases|Hypofibrinogenemia|not_provided": 1,
    "FIBRINOGEN_ISE": 1,
    "Afibrinogenemia|Congenital_afibrinogenemia|Hypofibrinogenemia|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_afibrinogenemia": 3,
    "not_provided|Congenital_afibrinogenemia": 14,
    "FIBRINOGEN_NIJMEGEN": 1,
    "FGB-related_disorder|Familial_dysfibrinogenemia|Congenital_afibrinogenemia": 1,
    "Familial_dysfibrinogenemia": 20,
    "FIBRINOGEN_NAPLES": 1,
    "FGB-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|FGB-related_disorder": 1,
    "not_provided|not_specified|FGB-related_disorder": 1,
    "Abnormal_bleeding": 10,
    "Familial_dysfibrinogenemia|FGB-related_disorder": 1,
    "Congenital_afibrinogenemia|not_specified": 1,
    "FGB-related_disorder|not_provided|Congenital_afibrinogenemia|Deep_venous_thrombosis": 1,
    "Congenital_afibrinogenemia|not_specified|not_provided": 2,
    "FIBRINOGEN_LONGMONT|Hypofibrinogenemia|FGB-related_disorder": 1,
    "not_provided|FGB-related_disorder": 1,
    "Congenital_afibrinogenemia|FGB-related_disorder|not_provided|Familial_dysfibrinogenemia|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Familial_dysfibrinogenemia|Congenital_afibrinogenemia": 1,
    "Familial_dysfibrinogenemia|not_provided|Congenital_afibrinogenemia": 1,
    "FGB-related_disorder|Congenital_afibrinogenemia": 1,
    "not_provided|Abnormal_bleeding|Thrombocytopenia|Hypofibrinogenemia|Congenital_afibrinogenemia|Afibrinogenemia|Thrombus|FGB-related_disorder|Familial_dysfibrinogenemia|not_specified": 1,
    "Hypofibrinogenemia": 8,
    "FIBRINOGEN_PONTOISE_2": 1,
    "Congenital_afibrinogenemia|not_provided": 4,
    "not_specified|not_provided|Congenital_afibrinogenemia": 1,
    "Familial_dysfibrinogenemia|Congenital_afibrinogenemia": 4,
    "Congenital_afibrinogenemia|not_provided|not_specified": 1,
    "Cerebral_cavernous_malformation": 277,
    "Congenital_fibrinogen_deficiency": 1,
    "FIBRINOGEN_BALTIMORE_2|Congenital_afibrinogenemia|not_provided|not_specified": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type": 38,
    "FGA-related_disorder": 19,
    "Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia": 55,
    "Inborn_genetic_diseases|FGA-related_disorder|AFib_amyloidosis": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia": 3,
    "Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 7,
    "Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Familial_dysfibrinogenemia|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Inborn_genetic_diseases|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia": 2,
    "Familial_dysfibrinogenemia|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Inborn_genetic_diseases": 1,
    "Familial_dysfibrinogenemia|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|not_provided": 1,
    "FGA-related_disorder|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Deep_venous_thrombosis|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|FIBRINOGEN_DUSART": 1,
    "Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|not_provided": 1,
    "Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|not_provided": 1,
    "Inborn_genetic_diseases|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "not_provided|Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|Congenital_afibrinogenemia": 1,
    "not_provided|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "FGA-related_disorder|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia": 2,
    "Afibrinogenemia": 2,
    "not_provided|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia": 1,
    "Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Inborn_genetic_diseases": 1,
    "FIBRINOGEN_MARBURG": 1,
    "Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "FIBRINOGEN_NIEUWEGEIN": 1,
    "Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Abnormal_bleeding|Thrombocytopenia|not_specified|FGA-related_disorder|not_provided": 1,
    "not_provided|FIBRINOGEN_CARACAS_2": 1,
    "FGA-related_disorder|Inborn_genetic_diseases": 1,
    "Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia": 1,
    "Inborn_genetic_diseases|Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Congenital_afibrinogenemia": 1,
    "not_provided|Afibrinogenemia|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "FIBRINOGEN_KEOKUK": 1,
    "not_specified|Venous_thromboembolism|_susceptibility_to|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|not_provided": 1,
    "not_provided|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|not_specified": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|Congenital_afibrinogenemia|not_provided|Hypofibrinogenemia": 1,
    "Inborn_genetic_diseases|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "FGA-related_disorder|Inborn_genetic_diseases|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|not_specified": 1,
    "not_provided|not_specified|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|Congenital_afibrinogenemia|Inborn_genetic_diseases": 2,
    "FGA-related_disorder|Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|Congenital_afibrinogenemia": 1,
    "Inborn_genetic_diseases|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|not_provided": 1,
    "FGA-related_disorder|not_specified|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|not_provided": 1,
    "Inborn_genetic_diseases|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia": 1,
    "FGA-related_disorder|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Familial_dysfibrinogenemia|Congenital_afibrinogenemia|FGA-related_disorder": 1,
    "Hypofibrinogenemia|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|not_provided|Familial_hypodysfibrinogenemia": 1,
    "not_provided|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia": 1,
    "not_specified|See_cases|Inborn_genetic_diseases": 1,
    "not_specified|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "FGA-related_disorder|Congenital_afibrinogenemia|not_provided": 1,
    "not_provided|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia": 1,
    "not_specified|FGA-related_disorder": 1,
    "Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|not_provided|not_specified|FGA-related_disorder|Familial_dysfibrinogenemia": 1,
    "not_specified|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|not_specified": 1,
    "Familial_dysfibrinogenemia|FGA-related_disorder|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Hypofibrinogenemia": 1,
    "FIBRINOGEN_CANTERBURY": 1,
    "FIBRINOGEN_DETROIT_1": 1,
    "not_provided|FIBRINOGEN_AARHUS_1|Hypofibrinogenemia|FGA-related_disorder": 1,
    "FIBRINOGEN_KYOTO_2": 1,
    "FGA-related_disorder|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Dysfibrinogenemia|Hypofibrinogenemia|Abnormal_bleeding": 1,
    "FIBRINOGEN_MUNICH_1": 1,
    "FGA-related_disorder|Familial_dysfibrinogenemia|not_provided|Dysfibrinogenemia": 1,
    "Afibrinogenemia|Familial_dysfibrinogenemia": 1,
    "Familial_dysfibrinogenemia|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "not_specified|Familial_dysfibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|FIBRINOGEN_ROUEN_1|not_provided": 1,
    "FIBRINOGEN_LILLE_1": 1,
    "Familial_dysfibrinogenemia|Congenital_afibrinogenemia|Familial_visceral_amyloidosis|_Ostertag_type|not_specified": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|not_provided": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Congenital_afibrinogenemia|Familial_dysfibrinogenemia|not_provided": 1,
    "Congenital_afibrinogenemia|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "not_specified|Congenital_afibrinogenemia": 2,
    "FGG-related_disorder|Congenital_afibrinogenemia|not_specified": 1,
    "Hypodysfibrinogenemia|not_provided": 1,
    "FGG-related_disorder": 6,
    "Hereditary_spastic_paraplegia_4|Congenital_afibrinogenemia|Familial_dysfibrinogenemia": 1,
    "FIBRINOGEN_OSAKA_5": 1,
    "See_cases|Afibrinogenemia": 1,
    "FIBRINOGEN_MATSUMOTO_1": 1,
    "Congenital_afibrinogenemia|FIBRINOGEN_PARIS_1|not_provided|FGG-related_disorder|not_specified": 1,
    "FGG-related_disorder|not_provided|not_specified": 1,
    "Familial_dysfibrinogenemia|Hypofibrinogenemia|not_specified|not_provided": 1,
    "FIBRINOGEN_MILANO_1": 1,
    "FIBRINOGEN_KYOTO_3": 1,
    "FIBRINOGEN_NAGOYA_1": 1,
    "FIBRINOGEN_VLISSINGEN_1": 1,
    "not_provided|FGG-related_disorder": 1,
    "Familial_dysfibrinogenemia|FIBRINOGEN_ASAHI|FGG-related_disorder|not_provided": 1,
    "FIBRINOGEN_KYOTO_1": 1,
    "not_provided|FIBRINOGEN_BALTIMORE_3": 1,
    "FGG-related_disorder|FIBRINOGEN_BALTIMORE_1": 1,
    "FIBRINOGEN_GIESSEN_4": 1,
    "FIBRINOGEN_HILLSBOROUGH": 1,
    "Familial_dysfibrinogenemia|Congenital_afibrinogenemia|not_provided|FIBRINOGEN_HAIFA_1|Hypofibrinogenemia": 1,
    "FGG-related_disorder|Familial_dysfibrinogenemia|not_provided|FIBRINOGEN_TOKYO_2|Afibrinogenemia|Hypofibrinogenemia": 1,
    "Congenital_afibrinogenemia|not_provided|Familial_dysfibrinogenemia": 1,
    "Familial_dysfibrinogenemia|Hypofibrinogenemia": 1,
    "Familial_dysfibrinogenemia|not_specified|Congenital_afibrinogenemia|Fibrinogen_Milano_XII|_digenic|Hypofibrinogenemia|not_provided": 1,
    "Hemorrhage|Inborn_genetic_diseases": 1,
    "Familial_dysfibrinogenemia|not_provided|Abnormal_bleeding": 1,
    "Thrombus|not_provided|Abnormal_bleeding|Thrombocytopenia|Congenital_fibrinogen_deficiency|Familial_dysfibrinogenemia|Congenital_afibrinogenemia|FGG-related_disorder|not_specified": 1,
    "Congenital_afibrinogenemia|not_specified|not_provided|FGG-related_disorder": 1,
    "Congenital_afibrinogenemia|FGG-related_disorder": 1,
    "FGG-related_disorder|not_specified|Congenital_afibrinogenemia|not_provided|Abnormal_bleeding": 1,
    "Congenital_afibrinogenemia|Hypofibrinogenemia": 1,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_14": 5,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_14": 9,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_14": 27,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_14|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_14|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_14": 1,
    "Leber_congenital_amaurosis_14|Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Leber_congenital_amaurosis_14|Retinitis_pigmentosa": 2,
    "Leber_congenital_amaurosis_14": 6,
    "Leber_congenital_amaurosis_1|not_provided": 11,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|not_provided": 2,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_14": 1,
    "Leber_congenital_amaurosis_14|LRAT-related_disorder|RETINITIS_PIGMENTOSA|_JUVENILE|_LRAT-RELATED|not_provided": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_14": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Leber_congenital_amaurosis_14": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Retinitis_pigmentosa|Leber_congenital_amaurosis_14|not_provided": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_14|not_provided|Leber_congenital_amaurosis": 2,
    "not_provided|Leber_congenital_amaurosis_1": 9,
    "Leber_congenital_amaurosis_14|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis_14": 2,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_14|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_14": 1,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_14": 2,
    "not_provided|LRAT-related_disorder": 2,
    "not_provided|RETINAL_DYSTROPHY|_EARLY-ONSET_SEVERE|_LRAT-RELATED": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_14|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_14|not_provided": 1,
    "not_specified|Leber_congenital_amaurosis_14": 1,
    "Retinitis_pigmentosa|LRAT-related_disorder|not_provided|Leber_congenital_amaurosis_14": 1,
    "RETINAL_DYSTROPHY|_EARLY-ONSET_SEVERE|_LRAT-RELATED|not_provided": 1,
    "Leber_congenital_amaurosis_14|Retinitis_pigmentosa|not_provided": 1,
    "LRAT-related_disorder|not_provided": 1,
    "Leber_congenital_amaurosis_14|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|Rod-cone_dystrophy|Leber_congenital_amaurosis_14": 1,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy": 6,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_14|Retinitis_pigmentosa": 5,
    "Retinitis_pigmentosa|Retinal_dystrophy|Leber_congenital_amaurosis_14": 3,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis|Leber_congenital_amaurosis_14": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_14|not_provided": 2,
    "Leber_congenital_amaurosis_14|Retinitis_pigmentosa|Leber_congenital_amaurosis": 5,
    "Retinal_dystrophy|Leber_congenital_amaurosis_14|Retinitis_pigmentosa": 5,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis": 2,
    "not_provided|Leber_congenital_amaurosis_14|Retinitis_pigmentosa|Leber_congenital_amaurosis": 2,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive": 1,
    "GUCY1A1-related_disorder|not_provided": 1,
    "Moyamoya_disease_1|Moyamoya_disease_with_early-onset_achalasia|not_specified|See_cases": 1,
    "not_provided|Moyamoya_disease_with_early-onset_achalasia": 1,
    "Moyamoya_disease_with_early-onset_achalasia": 9,
    "Moyamoya_disease_with_early-onset_achalasia|not_provided": 1,
    "Moyamoya_disease_with_early-onset_achalasia|Moyamoya_disease_1": 2,
    "ASIC5-related_disorder": 2,
    "Familial_hypertryptophanemia": 2,
    "TDO2-related_disorder": 4,
    "PDGFC-related_disorder": 1,
    "PDGFC-related_disorder|not_provided": 1,
    "Hyperekplexia_2": 328,
    "not_provided|Hyperekplexia_2": 20,
    "Hyperekplexia_2|Inborn_genetic_diseases": 15,
    "Inborn_genetic_diseases|Hyperekplexia_2": 12,
    "Inborn_genetic_diseases|GLRB-related_disorder|Hyperekplexia_2": 1,
    "not_provided|Hyperekplexia_2|Inborn_genetic_diseases|GLRB-related_disorder": 1,
    "Hyperekplexia_2|GLRB-related_disorder": 2,
    "Inborn_genetic_diseases|Hyperekplexia_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hyperekplexia_2": 1,
    "Hyperekplexia|Hyperekplexia_2": 1,
    "Hyperekplexia_2|not_provided": 2,
    "Hyperekplexia": 22,
    "Neurodevelopmental_disorder_with_language_impairment_and_behavioral_abnormalities": 46,
    "GRIA2-related_disorder": 5,
    "GRIA2-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_language_impairment_and_behavioral_abnormalities|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder_with_language_impairment_and_behavioral_abnormalities|not_provided": 4,
    "Inborn_genetic_diseases|GRIA2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_language_impairment_and_behavioral_abnormalities": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_language_impairment_and_behavioral_abnormalities": 1,
    "not_provided|Neurodevelopmental_disorder_with_language_impairment_and_behavioral_abnormalities": 2,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 39,
    "Glutaric_acidemia_IIc|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2C": 22,
    "Glutaric_acidemia_type_2C": 32,
    "not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 49,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 21,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_IIc": 3,
    "Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency": 25,
    "Inborn_genetic_diseases|ETFDH-related_disorder|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Glutaric_acidemia_type_2C|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Glutaric_acidemia_type_2C|Multiple_acyl-CoA_dehydrogenase_deficiency": 13,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "Glutaric_acidemia_type_2C|not_provided|not_specified|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|ETFDH-related_disorder|Abnormality_of_metabolism/homeostasis": 1,
    "Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 2,
    "ETFDH-related_disorder": 4,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided|Glutaric_acidemia_type_2C": 1,
    "Glutaric_acidemia_type_2C|not_provided": 2,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified|ETFDH-related_disorder": 1,
    "not_provided|Glutaric_acidemia_IIc|Multiple_acyl-CoA_dehydrogenase_deficiency|See_cases": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|ETFDH-related_disorder": 2,
    "not_provided|ETFDH-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency": 2,
    "Glutaric_acidemia_IIc|Glutaric_acidemia_type_2C|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|not_specified|Multiple_acyl-CoA_dehydrogenase_deficiency": 4,
    "ETFDH-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "ETFDH-related_disorder|not_specified|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency": 2,
    "ETFDH-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency": 2,
    "not_specified|Multiple_acyl-CoA_dehydrogenase_deficiency": 16,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided|Inborn_genetic_diseases": 4,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2C|not_specified": 2,
    "Glutaric_acidemia_type_2C|not_provided|Glutaric_acidemia_IIc|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 17,
    "ETFDH-related_disorder|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|Hypertrophic_cardiomyopathy": 1,
    "Glutaric_acidemia_type_2C|ETFDH-related_disorder": 1,
    "ETFDH-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "Glutaric_acidemia_iic|_late-onset|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|ETFDH-related_disorder|not_specified": 1,
    "Glutaric_acidemia_IIc|Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2C": 1,
    "not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 4,
    "ETFDH-related_disorder|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "not_specified|ETFDH-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_specified|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 6,
    "Glutaric_acidemia_iic|_late-onset": 1,
    "Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided|Glutaric_acidemia_type_2C": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 2,
    "ETFDH-related_disorder|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_specified|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 2,
    "ETFDH-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2C|ETFDH-related_disorder": 1,
    "Glutaric_acidemia_type_2C|Inborn_genetic_diseases|Glutaric_acidemia_iic|_late-onset|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Glutaric_acidemia_type_2C|Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Glutaric_acidemia_type_2C|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "not_provided|Glutaric_acidemia_type_2C|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2C|not_provided|Glutaric_acidemia_IIc": 1,
    "Glutaric_acidemia_iic|_late-onset|Glutaric_acidemia_type_2C|Acyl-CoA_dehydrogenase_deficiency|_glutaric_acidemia_type_II|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|ETFDH-related_disorder": 3,
    "not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 7,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|ETFDH-related_disorder|Glutaric_acidemia_type_2C": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided|Glutaric_acidemia_type_2C|ETFDH-related_disorder": 1,
    "Epilepsy|_familial_adult_myoclonic|_7": 9,
    "not_provided|Epilepsy|_familial_adult_myoclonic|_7": 2,
    "Small_for_gestational_age|Gestational_diabetes_mellitus_uncontrolled": 2,
    "NAF1-related_disorder": 9,
    "NAF1-related_disorder|not_provided|not_specified": 1,
    "not_provided|NAF1-related_disorder": 3,
    "Pulmonary_fibrosis|not_provided": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_7": 5,
    "NAF1-related_disorder|not_provided": 2,
    "not_specified|not_provided|NAF1-related_disorder": 2,
    "MSMO1-related_disorder|not_provided": 1,
    "Microcephaly-congenital_cataract-psoriasiform_dermatitis_syndrome": 5,
    "not_provided|MSMO1-related_disorder": 2,
    "Inborn_genetic_diseases|Microcephaly-congenital_cataract-psoriasiform_dermatitis_syndrome": 1,
    "CPE-related_disorder": 71,
    "CPE-related_disorder|not_specified": 1,
    "CPE-related_disorder|Inborn_genetic_diseases": 4,
    "BDV_syndrome": 3,
    "not_provided|CPE-related_disorder": 9,
    "Blakemore-Durmaz-Vasileiou_(BDV)_syndrome|BDV_syndrome": 1,
    "Inborn_genetic_diseases|CPE-related_disorder": 8,
    "not_provided|BDV_syndrome": 2,
    "CPE-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|CPE-related_disorder|not_provided": 2,
    "BDV_syndrome|not_provided": 1,
    "CPE-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "TLL1-related_disorder": 18,
    "Atrial_septal_defect_6": 16,
    "not_provided|Atrial_septal_defect_6": 1,
    "not_specified|TLL1-related_disorder": 1,
    "TLL1-related_disorder|not_specified": 1,
    "not_specified|Atrial_septal_defect_6": 1,
    "Atrial_septal_defect_6|not_specified": 1,
    "not_provided|TLL1-related_disorder": 2,
    "TLL1-related_disorder|Atrial_septal_defect_6|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_1": 62,
    "Pancreatic_cancer|_susceptibility_to|_1|not_provided": 1,
    "Carcinoma_of_pancreas": 21,
    "not_specified|Pancreatic_cancer|_susceptibility_to|_1": 28,
    "Pancreatic_cancer|_susceptibility_to|_1|not_specified|PALLD-related_disorder": 1,
    "not_specified|not_provided|Pancreatic_adenocarcinoma|Pancreatic_cancer|_susceptibility_to|_1": 4,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "PALLD-related_disorder": 9,
    "not_specified|PALLD-related_disorder": 14,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_1|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "Pancreatic_cancer|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|PALLD-related_disorder|not_specified|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "not_specified|Pancreatic_cancer|_susceptibility_to|_1|PALLD-related_disorder": 2,
    "PALLD-related_disorder|not_specified|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 7,
    "not_specified|PALLD-related_disorder|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 3,
    "not_provided|not_specified|Pancreatic_cancer|_susceptibility_to|_1": 2,
    "PALLD-related_disorder|not_specified": 8,
    "Pancreatic_cancer|_susceptibility_to|_1|not_specified": 4,
    "not_specified|Pancreatic_adenocarcinoma": 128,
    "not_provided|PALLD-related_disorder|Pancreatic_cancer|_susceptibility_to|_1": 3,
    "PALLD-related_disorder|not_specified|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "PALLD-related_disorder|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "PALLD-related_disorder|not_provided|not_specified": 1,
    "not_specified|PALLD-related_disorder|not_provided": 1,
    "Pancreatic_adenocarcinoma": 239,
    "Pancreatic_adenocarcinoma|not_provided": 2,
    "Pancreatic_adenocarcinoma|not_specified": 213,
    "not_specified|Pancreatic_cancer|_susceptibility_to|_1|not_provided|Pancreatic_adenocarcinoma": 1,
    "Pancreatic_adenocarcinoma|PALLD-related_disorder|not_specified": 3,
    "Pancreatic_adenocarcinoma|PALLD-related_disorder": 4,
    "Pancreatic_adenocarcinoma|not_specified|PALLD-related_disorder": 2,
    "PALLD-related_disorder|Pancreatic_cancer|_susceptibility_to|_1|not_specified|Pancreatic_adenocarcinoma": 1,
    "not_specified|PALLD-related_disorder|Pancreatic_adenocarcinoma": 4,
    "not_specified|Pancreatic_cancer|_susceptibility_to|_1|Pancreatic_adenocarcinoma": 9,
    "not_specified|Pancreatic_adenocarcinoma|not_provided": 2,
    "Pancreatic_adenocarcinoma|not_specified|not_provided": 4,
    "not_provided|Pancreatic_adenocarcinoma|PALLD-related_disorder": 1,
    "Pancreatic_adenocarcinoma|not_provided|PALLD-related_disorder|not_specified": 1,
    "Pancreatic_adenocarcinoma|not_specified|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 4,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_1|Pancreatic_adenocarcinoma|not_specified": 1,
    "PALLD-related_disorder|Pancreatic_adenocarcinoma|not_specified|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "not_specified|Pancreatic_adenocarcinoma|PALLD-related_disorder": 1,
    "PALLD-related_disorder|Pancreatic_adenocarcinoma|not_specified": 2,
    "Pancreatic_cancer|_susceptibility_to|_1|not_specified|Pancreatic_adenocarcinoma": 2,
    "PALLD-related_disorder|Pancreatic_adenocarcinoma": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Pancreatic_adenocarcinoma|Pancreatic_cancer|_susceptibility_to|_1|not_provided": 1,
    "Pancreatic_adenocarcinoma|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Pancreatic_adenocarcinoma": 1,
    "not_specified|not_provided|Pancreatic_adenocarcinoma": 3,
    "Pancreatic_cancer|_susceptibility_to|_1|Pancreatic_adenocarcinoma|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_adenocarcinoma|not_specified|Pancreatic_cancer|_susceptibility_to|_1": 2,
    "not_provided|Pancreatic_adenocarcinoma|not_specified": 1,
    "not_provided|not_specified|Pancreatic_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|PALLD-related_disorder|Pancreatic_adenocarcinoma|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pancreatic_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_1|PALLD-related_disorder|Pancreatic_adenocarcinoma|not_specified": 2,
    "Pancreatic_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Pancreatic_adenocarcinoma|Pancreatic_cancer|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_adenocarcinoma|Inborn_genetic_diseases": 1,
    "Pancreatic_adenocarcinoma|Pancreatic_cancer|_susceptibility_to|_1|not_specified": 2,
    "not_specified|Carcinoma_of_pancreas|Pancreatic_adenocarcinoma": 1,
    "PALLD-related_disorder|not_specified|Pancreatic_adenocarcinoma": 1,
    "PALLD-related_disorder|Pancreatic_adenocarcinoma|not_specified|not_provided|Pancreatic_cancer|_susceptibility_to|_1": 1,
    "Pancreatic_cancer|_susceptibility_to|_1|Pancreatic_adenocarcinoma|not_specified": 1,
    "Pancreatic_cancer|_susceptibility_to|_1|PALLD-related_disorder|not_specified|Pancreatic_adenocarcinoma": 1,
    "Carcinoma_of_pancreas|not_provided": 1,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_1": 3,
    "not_provided|Carcinoma_of_pancreas": 5,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 22,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 14,
    "NEK1-related_disorder": 38,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24": 9,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_specified": 5,
    "Short_rib-polydactyly_syndrome|NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Inborn_genetic_diseases|NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder": 19,
    "Connective_tissue_disorder|not_provided|not_specified|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "not_specified|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "NEK1-related_disorder|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 3,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|Inborn_genetic_diseases": 2,
    "NEK1-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_specified|Connective_tissue_disorder": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 13,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 3,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Mohr_syndrome|NEK1-related_disorder|not_specified": 1,
    "NEK1-related_disorder|Connective_tissue_disorder|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Asphyxiating_thoracic_dystrophy_1": 2,
    "NEK1-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|NEK1-related_disorder": 4,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|not_specified": 1,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder": 3,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Motor_neuron_disease": 2,
    "NEK1-related_disorder|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 3,
    "not_provided|not_specified|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 2,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_specified|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_specified|not_provided": 2,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Connective_tissue_disorder|not_provided": 2,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24": 3,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Inborn_genetic_diseases": 12,
    "NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Mohr_syndrome": 2,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|not_specified": 6,
    "NEK1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 14,
    "NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Motor_neuron_disease|NEK1-related_disorder": 3,
    "not_specified|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Motor_neuron_disease|not_provided": 2,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 2,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Motor_neuron_disease|NEK1-related_disorder": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Motor_neuron_disease|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "NEK1-related_disorder|not_specified|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "NEK1-related_disorder|Asphyxiating_thoracic_dystrophy_3": 1,
    "Short_rib-polydactyly_syndrome|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Connective_tissue_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|NEK1-related_disorder": 1,
    "Connective_tissue_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|not_specified": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|Connective_tissue_disorder": 1,
    "Mohr_syndrome|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|Motor_neuron_disease|not_provided|not_specified": 1,
    "Short_rib-polydactyly_syndrome|not_specified|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_specified": 2,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Mohr_syndrome": 1,
    "Connective_tissue_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|Motor_neuron_disease|not_specified|not_provided": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|NEK1-related_disorder": 4,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Connective_tissue_disorder": 1,
    "not_provided|NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Connective_tissue_disorder": 1,
    "Motor_neuron_disease|NEK1-related_disorder|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|not_specified|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Motor_neuron_disease|not_specified": 1,
    "Mohr_syndrome|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24": 1,
    "not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|not_specified": 1,
    "Mohr_syndrome": 1,
    "NEK1-related_disorder|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Connective_tissue_disorder|not_provided": 1,
    "Mohr_syndrome|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Type_IV_short_rib_polydactyly_syndrome": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Short_rib-polydactyly_syndrome|not_provided": 1,
    "Short_rib-polydactyly_syndrome|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|NEK1-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|Connective_tissue_disorder|Motor_neuron_disease|NEK1-related_disorder": 1,
    "not_provided|NEK1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_brain_abnormalities": 20,
    "CLCN3-related_disorder": 9,
    "Neurodevelopmental_disorder_with_hypotonia_and_brain_abnormalities|Neurodevelopmental_delay": 6,
    "Neurodevelopmental_disorder_with_seizures_and_brain_abnormalities|Neurodevelopmental_delay": 1,
    "Neurodevelopmental_disorder_with_seizures_and_brain_abnormalities|Neurodevelopmental_disorder_with_hypotonia_and_brain_abnormalities": 3,
    "CLCN3-related_disorder|not_provided": 1,
    "CLCN3-related_neurodevelopmental_disorders": 1,
    "Neurodevelopmental_delay|Neurodevelopmental_disorder_with_hypotonia_and_brain_abnormalities": 1,
    "not_provided|CLCN3-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_brain_abnormalities|Neurodevelopmental_disorder|Neurodevelopmental_delay": 1,
    "not_provided|HAND2-related_disorder": 2,
    "HAND2-related_disorder": 6,
    "HAND2-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|HAND2-related_disorder": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|not_provided|Isolated_congenital_digital_clubbing": 9,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing": 30,
    "Isolated_congenital_digital_clubbing|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1": 17,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing|not_provided": 2,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|HPGD-related_disorder|not_provided|Isolated_congenital_digital_clubbing": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|not_provided": 5,
    "not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1": 3,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1": 8,
    "Isolated_congenital_digital_clubbing|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|not_provided": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing|not_provided|HPGD-related_disorder": 1,
    "Isolated_congenital_digital_clubbing|not_provided": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|not_provided|Inborn_genetic_diseases|Isolated_congenital_digital_clubbing": 1,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Inborn_genetic_diseases|not_provided|Isolated_congenital_digital_clubbing": 1,
    "Inborn_genetic_diseases|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing|not_provided": 2,
    "not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing|HPGD-related_disorder": 1,
    "not_provided|Isolated_congenital_digital_clubbing|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1": 2,
    "not_provided|Cranioosteoarthropathy|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1": 1,
    "HPGD-related_disorder|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing|not_provided": 1,
    "not_provided|Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|Isolated_congenital_digital_clubbing": 3,
    "Hypertrophic_osteoarthropathy|_primary|_autosomal_recessive|_1|not_provided|not_specified|Isolated_congenital_digital_clubbing": 1,
    "VEGFC-related_disorder": 8,
    "Lymphatic_malformation_4": 6,
    "Lymphedema|Inborn_genetic_diseases": 1,
    "Lymphatic_malformation_4|not_provided": 2,
    "not_provided|Lymphatic_malformation_4": 1,
    "Low-frequency_hearing_loss|Low-frequency_sensorineural_hearing_impairment": 4,
    "Aspartylglucosaminuria": 454,
    "not_provided|Aspartylglucosaminuria": 12,
    "Aspartylglucosaminuria|not_provided": 15,
    "not_specified|Aspartylglucosaminuria": 3,
    "Aspartylglucosaminuria|Inborn_genetic_diseases": 9,
    "not_specified|not_provided|Aspartylglucosaminuria|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Aspartylglucosaminuria": 2,
    "Inborn_genetic_diseases|Aspartylglucosaminuria": 5,
    "not_specified|not_provided|Aspartylglucosaminuria": 2,
    "Aspartylglucosaminuria|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Aspartylglucosaminuria": 1,
    "Aspartylglucosaminuria|AGA-related_disorder|not_provided": 1,
    "AGA-related_disorder": 1,
    "Aspartylglucosaminuria|_finnish_type|Aspartylglucosaminuria": 1,
    "Aspartylglucosaminuria|not_provided|Intellectual_disability": 1,
    "Aspartylglucosaminuria|Neurodevelopmental_disorder|Intellectual_disability": 1,
    "not_provided|Aspartylglucosaminuria|AGA-related_disorder|not_specified": 1,
    "Aspartylglucosaminuria|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Autism|Aspartylglucosaminuria": 1,
    "not_provided|not_specified|Aspartylglucosaminuria": 1,
    "AGA-related_disorder|Aspartylglucosaminuria": 1,
    "Aspartylglucosaminuria|Inborn_genetic_diseases|AGA-related_disorder": 1,
    "Intellectual_disability|not_provided|Aspartylglucosaminuria": 1,
    "not_provided|TENM3-related_disorder": 7,
    "TENM3-related_disorder": 13,
    "Microphthalmia|_isolated|_with_coloboma_9": 14,
    "not_provided|TENM3-related_disorder|Inborn_genetic_diseases": 1,
    "Microphthalmia|_isolated|_with_coloboma_9|TENM3-related_disorder|Inborn_genetic_diseases": 1,
    "Microphthalmia|_isolated|_with_coloboma_9|not_provided": 4,
    "not_specified|Microphthalmia|_isolated|_with_coloboma_9|not_provided": 2,
    "MICROPHTHALMIA|_SYNDROMIC_15": 2,
    "Inborn_genetic_diseases|not_provided|TENM3-related_disorder": 1,
    "TENM3-related_disorder|not_provided": 8,
    "Inborn_genetic_diseases|Meniere_disease": 2,
    "MICROPHTHALMIA|_SYNDROMIC_15|Microphthalmia|_isolated|_with_coloboma_9": 2,
    "Inborn_genetic_diseases|Microphthalmia|_isolated|_with_coloboma_9": 2,
    "Meniere_disease|Inborn_genetic_diseases": 4,
    "not_provided|TRAPPC11-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 629,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 28,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 27,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided": 39,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided|not_specified": 8,
    "TRAPPC11-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_specified|not_provided": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_specified": 3,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|TRAPPC11-related_disorder": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|Inborn_genetic_diseases": 26,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided|TRAPPC11-related_disorder": 2,
    "Limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 2,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|TRAPPC11-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 1,
    "TRAPPC11-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 1,
    "TRAPPC11-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|TRAPPC11-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_specified|not_provided": 1,
    "TRAPPC11-related_disorder": 2,
    "Muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|Inborn_genetic_diseases": 2,
    "not_provided|TRAPPC11-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_R18|not_specified": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 23,
    "PRIMPOL-related_disorder": 12,
    "PRIMPOL-related_disorder|not_provided": 1,
    "not_specified|Myopia_22|_autosomal_dominant": 2,
    "Myopia_22|_autosomal_dominant": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions": 9,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2": 46,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2": 9,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive": 8,
    "not_specified|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2": 2,
    "SLC25A4-related_disorder": 3,
    "Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive": 9,
    "Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant": 4,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|not_provided|Mitochondrial_disease": 1,
    "Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive|not_provided|not_specified|SLC25A4-related_disorder": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|not_provided": 1,
    "not_provided|SLC25A4-related_disorder": 4,
    "Vertigo|Myopia|Progressive_sensorineural_hearing_impairment|Hypertrophic_cardiomyopathy|Mitochondrial_respiratory_chain_defects|Abnormality_of_mitochondrial_metabolism|Inborn_mitochondrial_myopathy|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Left_ventricular_hypertrophy": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive": 2,
    "SLC25A4-related_disorder|not_provided": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant": 1,
    "Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive|SLC25A4-related_disorder|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2": 1,
    "not_provided|not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2": 2,
    "Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|Mitochondrial_disease": 1,
    "not_provided|Family_history_of_sudden_cardiac_death": 1,
    "Restrictive_cardiomyopathy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|not_provided": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2": 1,
    "SLC25A4-related_disorder|not_provided|not_specified": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_2|Mitochondrial_DNA_depletion_syndrome_12B_(cardiomyopathic_type)|_autosomal_recessive|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant": 6,
    "SNX25-related_autism_spectrum_disorder": 1,
    "Hip_dysplasia|_Beukes_type|not_provided": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_di_rocco_type": 1,
    "Spondyloepimetaphyseal_dysplasia|_di_rocco_type|Hip_dysplasia|_Beukes_type": 1,
    "UFSP2-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy_106": 3,
    "Spondyloepimetaphyseal_dysplasia|_di_rocco_type|Hip_dysplasia|_Beukes_type|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_di_rocco_type": 1,
    "Hip_dysplasia|_Beukes_type": 1,
    "UFSP2-related_neurodevelopmental_disorder|not_provided|Abnormality_of_the_nervous_system|Developmental_and_epileptic_encephalopathy_106|Hip_dysplasia|_Beukes_type|Developmental_and_epileptic_encephalopathy|_1|Focal-onset_seizure|Epileptic_encephalopathy|Severe_global_developmental_delay|Seizure|Intellectual_disability|Microcephaly|Olivopontocerebellar_hypoplasia": 1,
    "Spondyloepimetaphyseal_dysplasia|_di_rocco_type|not_provided|Hip_dysplasia|_Beukes_type": 2,
    "Hip_dysplasia|_Beukes_type|Developmental_and_epileptic_encephalopathy_106|Spondyloepimetaphyseal_dysplasia|_di_rocco_type": 1,
    "not_provided|UFSP2-related_disorder": 1,
    "not_provided|Hip_dysplasia|_Beukes_type": 1,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified": 15,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 31,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 117,
    "not_specified|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 17,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 55,
    "not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 2,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 8,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified|not_provided": 3,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|PDLIM3-related_disorder|not_specified|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|not_specified": 5,
    "not_provided|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided": 5,
    "not_specified|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 3,
    "not_specified|Primary_familial_hypertrophic_cardiomyopathy": 82,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided": 2,
    "Familial_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "PDLIM3-related_disorder|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided": 3,
    "not_specified|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|PDLIM3-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_specified|PDLIM3-related_disorder|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|PDLIM3-related_disorder": 1,
    "Restrictive_cardiomyopathy|not_specified": 1,
    "PDLIM3-related_disorder": 2,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|PDLIM3-related_disorder": 1,
    "not_provided|not_specified|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 2,
    "not_provided|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided": 2,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_1|not_specified": 3,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1": 720,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|not_specified": 28,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|not_provided": 12,
    "Immunodeficiency_83|_susceptibility_to_viral_infections|Herpes_simplex_encephalitis|_susceptibility_to|_1": 4,
    "TLR3-related_disorder|Herpes_simplex_encephalitis|_susceptibility_to|_1": 3,
    "not_specified|not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_1": 4,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|Immunodeficiency_83|_susceptibility_to_viral_infections|Susceptibility_to_HIV_infection": 1,
    "TLR3-related_disorder": 2,
    "not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_1": 28,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_1": 30,
    "Susceptibility_to_HIV_infection|Immunodeficiency_83|_susceptibility_to_viral_infections|Herpes_simplex_encephalitis|_susceptibility_to|_1": 1,
    "not_provided|Immunodeficiency_83|_susceptibility_to_viral_infections|Herpes_simplex_encephalitis|_susceptibility_to|_1": 1,
    "TLR3-related_disorder|not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_1": 2,
    "Hepatitis_C_virus|_susceptibility_to": 5,
    "Immunodeficiency_83|_susceptibility_to_viral_infections|Susceptibility_to_HIV_infection|Multisystem_inflammatory_syndrome_in_children|Herpes_simplex_encephalitis|_susceptibility_to|_1|not_provided": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|TLR3-related_disorder": 3,
    "Immunodeficiency_83|_susceptibility_to_viral_infections": 6,
    "Immunodeficiency_83|_susceptibility_to_viral_infections|not_specified|not_provided|Susceptibility_to_HIV_infection|Herpes_simplex_encephalitis|_susceptibility_to|_1|TLR3-related_disorder": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|TLR3-related_disorder|not_provided|Immunodeficiency_83|_susceptibility_to_viral_infections|Susceptibility_to_HIV_infection|not_specified": 1,
    "not_specified|Immunodeficiency_83|_susceptibility_to_viral_infections|Susceptibility_to_HIV_infection|Herpes_simplex_encephalitis|_susceptibility_to|_1": 1,
    "not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_1|not_provided": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|Immunodeficiency_83|_susceptibility_to_viral_infections": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|not_specified|Immunodeficiency_83|_susceptibility_to_viral_infections": 1,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_1|TLR3-related_disorder": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Corneal_Dystrophy|_Recessive": 12,
    "Bietti_crystalline_corneoretinal_dystrophy|Corneal_Dystrophy|_Recessive|not_provided": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy": 29,
    "Corneal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy": 39,
    "Corneal_dystrophy|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 22,
    "Corneal_Dystrophy|_Recessive|Bietti_crystalline_corneoretinal_dystrophy": 4,
    "Retinal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy|not_provided": 1,
    "Corneal_dystrophy|Retinal_dystrophy|not_specified|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 2,
    "Corneal_dystrophy|CYP4V2-related_disorder|Bietti_crystalline_corneoretinal_dystrophy|not_provided": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Bietti_crystalline_corneoretinal_dystrophy": 13,
    "not_provided|Retinal_dystrophy|Corneal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy": 2,
    "Corneal_dystrophy|not_specified|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 6,
    "not_provided|Bietti_crystalline_corneoretinal_dystrophy|Retinal_dystrophy|Corneal_dystrophy": 2,
    "Retinal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy|not_provided|CYP4V2-related_disorder": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|not_provided|Corneal_dystrophy": 3,
    "Inborn_genetic_diseases|Corneal_dystrophy|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 2,
    "not_provided|Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy": 3,
    "not_provided|Bietti_crystalline_corneoretinal_dystrophy|Retinal_dystrophy": 1,
    "Corneal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy|not_provided": 2,
    "Bietti_crystalline_corneoretinal_dystrophy|not_provided": 2,
    "Retinal_dystrophy|not_specified|Bietti_crystalline_corneoretinal_dystrophy|not_provided|Corneal_dystrophy": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Retinal_dystrophy": 1,
    "Choroideremia|Retinal_dystrophy": 1,
    "not_provided|Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy|not_specified": 1,
    "Corneal_dystrophy|Retinal_dystrophy|not_provided|Bietti_crystalline_corneoretinal_dystrophy|not_specified": 1,
    "not_specified|Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "Optic_atrophy|Retinal_dystrophy": 4,
    "Bietti_crystalline_corneoretinal_dystrophy|not_provided|Inborn_genetic_diseases|Corneal_dystrophy": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Inborn_genetic_diseases|not_provided|Corneal_dystrophy": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|not_provided|Retinal_dystrophy": 1,
    "not_provided|CYP4V2-related_disorder": 1,
    "Corneal_dystrophy|Inborn_genetic_diseases|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy|not_specified|not_provided": 1,
    "CYP4V2-related_disorder|Corneal_dystrophy|Retinal_dystrophy|Bietti_crystalline_corneoretinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|Bietti_crystalline_corneoretinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Bietti_crystalline_corneoretinal_dystrophy|Corneal_dystrophy": 1,
    "CYP4V2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "Corneal_dystrophy|not_specified|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "not_provided|Bietti_crystalline_corneoretinal_dystrophy|Corneal_Dystrophy|_Recessive": 4,
    "Corneal_Dystrophy|_Recessive|Bietti_crystalline_corneoretinal_dystrophy|not_provided": 1,
    "Corneal_Dystrophy|_Recessive|not_provided|Bietti_crystalline_corneoretinal_dystrophy": 1,
    "Inherited_prekallikrein_deficiency": 10,
    "Prekallikrein_deficiency": 3,
    "Inherited_prekallikrein_deficiency|not_specified|Hypophosphatemic_rickets_and_hyperparathyroidism|Prekallikrein_deficiency|not_provided": 1,
    "Prekallikrein_deficiency|KLKB1-related_disorder|Inherited_prekallikrein_deficiency|not_provided": 1,
    "Inherited_prekallikrein_deficiency|not_provided": 2,
    "KLKB1-related_disorder": 6,
    "not_specified|not_provided|KLKB1-related_disorder": 1,
    "not_provided|KLKB1-related_disorder": 1,
    "not_provided|Inherited_prekallikrein_deficiency": 1,
    "KLKB1-related_disorder|Inherited_prekallikrein_deficiency": 1,
    "Prekallikrein_deficiency|Inherited_prekallikrein_deficiency": 1,
    "KLKB1-related_disorder|not_provided": 2,
    "Prekallikrein_deficiency|Inherited_prekallikrein_deficiency|not_provided": 1,
    "Plasma_factor_XI_deficiency": 51,
    "Hereditary_factor_XI_deficiency_disease": 149,
    "F11-related_disorder": 5,
    "not_provided|Hereditary_factor_XI_deficiency_disease": 57,
    "Plasma_factor_XI_deficiency|Hereditary_factor_XI_deficiency_disease": 2,
    "Plasma_factor_XI_deficiency|not_provided|Hereditary_factor_XI_deficiency_disease": 9,
    "Hereditary_factor_XI_deficiency_disease|not_provided": 16,
    "not_provided|Plasma_factor_XI_deficiency|Hereditary_factor_XI_deficiency_disease": 3,
    "Plasma_factor_XI_deficiency|not_provided": 10,
    "Plasma_factor_XI_deficiency|F11-related_disorder|not_provided": 2,
    "not_specified|not_provided|Hereditary_factor_XI_deficiency_disease": 3,
    "Factor_XI_deficiency|not_provided|Plasma_factor_XI_deficiency|Hereditary_factor_XI_deficiency_disease": 1,
    "Plasma_factor_XI_deficiency|Hereditary_factor_XI_deficiency_disease|not_provided": 5,
    "F11-related_disorder|Plasma_factor_XI_deficiency|not_provided": 2,
    "not_specified|Hereditary_factor_XI_deficiency_disease|not_provided": 3,
    "Hereditary_factor_XI_deficiency_disease|not_specified": 1,
    "Plasma_factor_XI_deficiency|not_provided|Hereditary_factor_XI_deficiency_disease|Abnormal_bleeding": 1,
    "F11-related_disorder|Plasma_factor_XI_deficiency|Inborn_genetic_diseases|not_provided|Hereditary_factor_XI_deficiency_disease|Abnormal_bleeding|Thrombocytopenia": 1,
    "not_provided|Abnormal_bleeding|Hereditary_factor_XI_deficiency_disease": 1,
    "Plasma_factor_XI_deficiency|not_provided|Hereditary_factor_XI_deficiency_disease|not_specified": 1,
    "not_provided|F11-related_disorder": 3,
    "Hereditary_factor_XI_deficiency_disease|Plasma_factor_XI_deficiency|not_provided": 5,
    "F11-related_disorder|not_provided": 1,
    "F11-related_disorder|not_provided|Hereditary_factor_XI_deficiency_disease": 4,
    "Abnormal_bleeding|Hereditary_factor_XI_deficiency_disease": 1,
    "Plasma_factor_XI_deficiency|Hereditary_factor_XI_deficiency_disease|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Plasma_factor_XI_deficiency": 1,
    "not_provided|not_specified|Hereditary_factor_XI_deficiency_disease|Plasma_factor_XI_deficiency": 1,
    "not_provided|Plasma_factor_XI_deficiency": 5,
    "Factor_XI|Plasma_factor_XI_deficiency|F11-related_disorder|not_provided|Hereditary_factor_XI_deficiency_disease": 1,
    "not_provided|Hereditary_factor_XI_deficiency_disease|F11-related_disorder": 1,
    "F11-related_disorder|Plasma_factor_XI_deficiency|not_provided|Hereditary_factor_XI_deficiency_disease": 2,
    "F11-related_disorder|Hereditary_factor_XI_deficiency_disease": 1,
    "Plasma_factor_XI_deficiency|not_specified|Hereditary_factor_XI_deficiency_disease|not_provided": 1,
    "Plasma_factor_XI_deficiency|not_provided|Hereditary_factor_XI_deficiency_disease|F11-related_disorder": 1,
    "Coagulation_factor_deficiency_syndrome|Hereditary_factor_XI_deficiency_disease|not_provided": 1,
    "not_specified|Hereditary_factor_XI_deficiency_disease": 2,
    "Inborn_genetic_diseases|Hereditary_factor_XI_deficiency_disease": 1,
    "Hereditary_factor_XI_deficiency_disease|not_specified|F11-related_disorder|Plasma_factor_XI_deficiency|not_provided": 1,
    "F11-related_disorder|Plasma_factor_XI_deficiency|not_specified|Hereditary_factor_XI_deficiency_disease|not_provided": 1,
    "Plasma_factor_XI_deficiency|not_provided|Abnormal_bleeding|Hereditary_factor_XI_deficiency_disease": 1,
    "not_specified|Inborn_genetic_diseases|Plasma_factor_XI_deficiency": 1,
    "not_provided|Hereditary_factor_XI_deficiency_disease|Plasma_factor_XI_deficiency": 2,
    "Plasma_factor_XI_deficiency|not_specified|not_provided|Hereditary_factor_XI_deficiency_disease": 1,
    "not_provided|Plasma_factor_XI_deficiency|not_specified|Hereditary_factor_XI_deficiency_disease": 1,
    "FAT1-related_disorder": 89,
    "not_provided|FAT1-related_disorder": 53,
    "FAT1-related_disorder|Inborn_genetic_diseases": 2,
    "FAT1-related_disorder|not_provided": 43,
    "Inborn_genetic_diseases|FAT1-related_disorder": 5,
    "Focal_and_Segmental_Glomerulosclerosis|_Autosomal_recessive": 1,
    "FAT1-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Glomerulotubular_Nephropathy": 1,
    "not_provided|FAT1-related_disorder|Inborn_genetic_diseases": 4,
    "Intellectual_disability|_moderate|Attention_deficit_hyperactivity_disorder|Delayed_speech_and_language_development|Spasticity|Hypertensive_disorder": 1,
    "Focal_segmental_glomerulosclerosis|FAT1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|FAT1-related_disorder": 5,
    "FAT1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|FAT1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_moderate|Attention_deficit_hyperactivity_disorder|Hypertensive_disorder|Delayed_speech_and_language_development|Spasticity": 1,
    "not_provided|Inborn_genetic_diseases|FAT1-related_disorder": 5,
    "FAT1-related_disorder|not_provided|not_specified": 1,
    "FAT1-related_disorder|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "Nephrotic_syndrome|not_provided": 5,
    "not_specified|not_provided|FAT1-related_disorder": 2,
    "not_provided|Irido-corneo-trabecular_dysgenesis|Anophthalmia-microphthalmia_syndrome": 1,
    "FAT1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Multiple_myeloma": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|Inborn_genetic_diseases": 3,
    "Familial_idiopathic_steroid-resistant_nephrotic_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Focal_and_Segmental_Glomerulosclerosis|_Autosomal_recessive": 1,
    "FRG1-related_disorder": 5,
    "Pulmonary_artery_atresia": 12,
    "Pheochromocytoma|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Pheochromocytoma|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5": 116,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 9,
    "Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 3,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 672,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 26,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 171,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 200,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 46,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 227,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 339,
    "Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 22,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Leigh_syndrome": 1,
    "Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 4,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 212,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 3,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 4,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 5,
    "Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 7,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 20,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 12,
    "Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 3,
    "Dilated_cardiomyopathy_1GG": 15,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_specified": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_specified": 4,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Rhabdomyosarcoma|Carney_triad|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Pilocytic_astrocytoma|Leigh_syndrome|Intellectual_disability": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided|SDHA-related_disorder": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Gastrointestinal_stromal_tumor|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Dilated_cardiomyopathy_1GG": 3,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 6,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 3,
    "not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_renal_cell_carcinoma|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Leigh_syndrome|SDHA-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 2,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG": 7,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 8,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome": 1,
    "Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 11,
    "Dilated_cardiomyopathy_1GG|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Dilated_cardiomyopathy_1GG|SDHA-related_disorder": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG": 4,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 10,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor": 1,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 9,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 15,
    "Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "B-lymphoblastic_leukemia/lymphoma_with_hypodiploidy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG": 1,
    "Dilated_cardiomyopathy_1GG|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Carney_triad": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 3,
    "not_specified|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 5,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 5,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 3,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 11,
    "not_provided|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Pheochromocytoma/paraganglioma_syndrome_4|Incidental_Discovery|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 2,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 5,
    "not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|not_specified": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Leigh_syndrome|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 6,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG": 4,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 2,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5": 2,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_specified": 3,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_provided": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|SDHA-related_disorder": 3,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG": 9,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG": 6,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 3,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 2,
    "Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Dilated_cardiomyopathy_1GG|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome": 2,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Gastrointestinal_stromal_tumor": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|Dilated_cardiomyopathy_1GG|not_provided": 2,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Leigh_syndrome": 1,
    "not_specified|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|SDHA-related_disorder": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Gastrointestinal_stromal_tumor": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neoplasm_of_brain|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Skeletal_myopathy": 1,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cancer_or_benign_tumor": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Dilated_cardiomyopathy_1GG|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 4,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder": 2,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 2,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5": 6,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Leigh_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Leigh_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Dilated_cardiomyopathy_1GG": 1,
    "Dilated_cardiomyopathy_1GG|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 1,
    "not_specified|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome|SDHA-related_disorder": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 1,
    "SDHA-related_disorder|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 3,
    "Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Sick_sinus_syndrome_2|_autosomal_dominant|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_specified": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 4,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_provided|SDHA-related_disorder|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 2,
    "not_provided|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Gastrointestinal_stromal_tumor": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Dilated_cardiomyopathy_1GG|Leigh_syndrome|SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Primary_dilated_cardiomyopathy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1": 12,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG": 1,
    "Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_provided|not_specified|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 2,
    "Dilated_cardiomyopathy_1GG|Childhood_neoplasm|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Paraganglioma|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pulmonary_artery_atresia": 1,
    "Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Pulmonary_artery_atresia|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Gastrointestinal_stromal_tumor|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|SDHA-related_disorder": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|not_specified|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Pheochromocytoma|Paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Leigh_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma|Gastrointestinal_stromal_tumor|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1GG": 1,
    "Opsoclonus-myoclonus_syndrome|Hereditary_pheochromocytoma-paraganglioma|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_specified|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_provided": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|not_specified|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Dilated_cardiomyopathy_1GG": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|SDHA-related_disorder|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Gastrointestinal_stromal_tumor|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|SDHA-related_disorder|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 1,
    "not_specified|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|not_specified|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided|Leigh_syndrome": 1,
    "SDHA-related_disorder|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|Gastrointestinal_stromal_tumor|not_provided|Dilated_cardiomyopathy_1GG": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Dilated_cardiomyopathy_1GG|Intellectual_disability": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Gastrointestinal_stromal_tumor|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Gastrointestinal_stromal_tumor|Dilated_cardiomyopathy_1GG": 1,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Gastrointestinal_stromal_tumor": 1,
    "Hereditary_cancer-predisposing_syndrome|See_cases|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Leigh_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|SDHA-related_disorder": 1,
    "Dilated_cardiomyopathy_1GG|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Gastrointestinal_stromal_tumor|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|SDHA-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|SDHA-related_disorder|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|not_specified|Pheochromocytoma|SDHA-related_disorder|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "SDHA-related_disorder|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Leigh_syndrome|Dilated_cardiomyopathy_1GG|not_provided": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|not_specified|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_provided|SDHA-related_disorder|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_provided|SDHA-related_disorder|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_specified|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5": 2,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Dilated_cardiomyopathy_1GG|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|not_provided|Leigh_syndrome|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Dilated_cardiomyopathy_1GG": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|not_specified|SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 2,
    "Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Dilated_cardiomyopathy_1GG|Hereditary_cancer-predisposing_syndrome|Leigh_syndrome|SDHA-related_disorder|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "SDHA-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_5|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "SDHA-related_disorder|Pheochromocytoma/paraganglioma_syndrome_5": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Leigh_syndrome|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Leigh_syndrome|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Dilated_cardiomyopathy_1GG|Pheochromocytoma/paraganglioma_syndrome_5|Neurodegeneration_with_ataxia_and_late-onset_optic_atrophy|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma|Leigh_syndrome": 1,
    "Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma|not_provided|Leigh_syndrome": 1,
    "Congenital_secretory_sodium_diarrhea_8|not_provided": 9,
    "SLC9A3-related_disorder": 5,
    "SLC9A3-related_disorder|not_provided": 12,
    "not_provided|Congenital_secretory_sodium_diarrhea_8": 7,
    "not_provided|SLC9A3-related_disorder": 7,
    "Congenital_secretory_sodium_diarrhea_8": 13,
    "not_provided|SLC9A3-related_disorder|Congenital_secretory_sodium_diarrhea_8": 1,
    "SLC9A3-related_disorder|Congenital_secretory_sodium_diarrhea_8|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_secretory_sodium_diarrhea_8|not_provided": 1,
    "Congenital_secretory_sodium_diarrhea_8|SLC9A3-related_disorder|not_provided": 1,
    "Congenital_secretory_sodium_diarrhea_8|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|SLC9A3-related_disorder|not_specified": 1,
    "not_provided|TRIP13-related_disorder": 10,
    "not_provided|Oocyte_maturation_defect_9|Mosaic_variegated_aneuploidy_syndrome_3": 1,
    "TRIP13-related_disorder|not_provided": 5,
    "Mosaic_variegated_aneuploidy_syndrome_3|Oocyte_maturation_defect_9": 2,
    "Oocyte_maturation_defect_9|not_provided|Mosaic_variegated_aneuploidy_syndrome_3": 1,
    "TRIP13-related_disorder": 6,
    "TRIP13-related_disorder|not_specified": 1,
    "Oocyte_maturation_defect_9": 3,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_3|Oocyte_maturation_defect_9": 1,
    "Mosaic_variegated_aneuploidy_syndrome_3": 5,
    "Mosaic_variegated_aneuploidy_syndrome_3|not_provided": 1,
    "Oocyte_maturation_defect_9|not_provided": 1,
    "not_specified|not_provided|TRIP13-related_disorder": 1,
    "not_specified|TRIP13-related_disorder": 1,
    "not_provided|SLC6A19-related_disorder": 6,
    "Neutral_1_amino_acid_transport_defect": 86,
    "Neutral_1_amino_acid_transport_defect|not_provided": 23,
    "Inborn_genetic_diseases|Neutral_1_amino_acid_transport_defect|not_provided": 4,
    "Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|not_provided": 17,
    "Neutral_1_amino_acid_transport_defect|Iminoglycinuria|Hyperglycinuria|not_provided": 6,
    "not_provided|Neutral_1_amino_acid_transport_defect": 24,
    "not_provided|Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|SLC6A19-related_disorder": 1,
    "not_provided|SLC6A19-related_disorder|Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria": 1,
    "not_provided|Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria": 16,
    "not_specified|Neutral_1_amino_acid_transport_defect|not_provided": 1,
    "Neutral_1_amino_acid_transport_defect|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Neutral_1_amino_acid_transport_defect": 2,
    "Neutral_1_amino_acid_transport_defect|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|Hyperglycinuria|Inborn_genetic_diseases": 1,
    "SLC6A19-related_disorder|Iminoglycinuria|Neutral_1_amino_acid_transport_defect|Hyperglycinuria|not_specified|not_provided": 1,
    "Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|SLC6A19-related_disorder|not_provided": 1,
    "SLC6A19-related_disorder|not_provided": 5,
    "not_provided|Neutral_1_amino_acid_transport_defect|Hyperglycinuria": 1,
    "Inborn_genetic_diseases|Neutral_1_amino_acid_transport_defect": 2,
    "not_provided|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|Hyperglycinuria": 3,
    "Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria": 1,
    "Iminoglycinuria|Neutral_1_amino_acid_transport_defect|Hyperglycinuria|not_provided": 1,
    "SLC6A19-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Hyperglycinuria|Iminoglycinuria|Neutral_1_amino_acid_transport_defect|not_provided": 1,
    "not_specified|not_provided|Neutral_1_amino_acid_transport_defect": 1,
    "Inborn_genetic_diseases|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|Hyperglycinuria|not_provided": 1,
    "not_specified|not_provided|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|_digenic|Hyperglycinuria": 1,
    "Hyperglycinuria|Neutral_1_amino_acid_transport_defect|Iminoglycinuria|not_specified|not_provided": 1,
    "not_provided|Neutral_1_amino_acid_transport_defect|SLC6A19-related_disorder": 1,
    "Iminoglycinuria|Neutral_1_amino_acid_transport_defect|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|High_myopia|Neutral_1_amino_acid_transport_defect|Hyperglycinuria": 1,
    "SLC6A19-related_disorder": 2,
    "SLC6A18-related_condition": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 3,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 4,
    "Interstitial_lung_disease_2": 43,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia": 1,
    "Aplastic_anemia|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided": 1,
    "Aplastic_anemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "TERT-related_disorder": 12,
    "not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Dyskeratosis_congenita": 2764,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 861,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita": 291,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 383,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 250,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 165,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided": 11,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder|not_provided|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2": 7,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Dyskeratosis_congenita": 42,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_provided|Dyskeratosis_congenita": 5,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 167,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder": 3,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Interstitial_lung_disease_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|not_provided": 9,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 2,
    "Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "not_provided|Dyskeratosis_congenita": 60,
    "TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "Dyskeratosis_congenita|not_provided": 53,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|not_provided|not_specified|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|not_specified": 4,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Interstitial_lung_disease_2|Dyskeratosis_congenita|_autosomal_dominant_1|Aplastic_anemia|Acute_myeloid_leukemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita": 1,
    "not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|TERT-related_disorder|Dyskeratosis_congenita": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified": 3,
    "Interstitial_lung_disease_2|Dyskeratosis_congenita|_autosomal_dominant_2": 6,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Dyskeratosis_congenita": 15,
    "Dyskeratosis_congenita|not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 4,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Pulmonary_fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Leukemia|_acute_myeloid|_susceptibility_to|Aplastic_anemia|Breast_carcinoma": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided": 7,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder": 3,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 8,
    "not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita": 5,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_specified|not_provided|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|TERT-related_disorder": 7,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|TERT-related_disorder": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Telomere_syndrome": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|Dyskeratosis_congenita": 7,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|DiGeorge_syndrome|Aplastic_anemia": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 9,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 3,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified": 6,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|TERT-related_disorder": 5,
    "Dyskeratosis_congenita|_autosomal_dominant_2": 18,
    "not_specified|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 4,
    "not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Acute_myeloid_leukemia|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 10,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder": 5,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Pulmonary_fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Acute_myeloid_leukemia|Aplastic_anemia": 1,
    "TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided": 12,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Idiopathic_Pulmonary_Fibrosis|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|not_provided": 4,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Microcephaly": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 6,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "not_provided|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 9,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Aplastic_anemia": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Dyskeratosis_congenita": 24,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Interstitial_lung_disease_2|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided": 8,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|not_specified": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Dyskeratosis_congenita": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Short_telomere_length|Macrocytic_anemia|Premature_graying_of_hair|Abnormal_pulmonary_interstitial_morphology|not_provided|Pulmonary_fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Dyskeratosis_congenita": 6,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|not_specified|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|not_specified|Dyskeratosis_congenita": 5,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita": 1,
    "not_specified|Dyskeratosis_congenita": 21,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita": 3,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Autosomal_recessive_dyskeratosis_congenita_4|Dyskeratosis_congenita|_autosomal_recessive_1": 1,
    "Dyskeratosis_congenita|TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|TERT-related_disorder": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_specified|not_provided|Dyskeratosis_congenita": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 3,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Pulmonary_fibrosis": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Interstitial_lung_disease_2": 1,
    "Telomere_syndrome|not_specified|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder|Dyskeratosis_congenita": 4,
    "Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Interstitial_lung_disease_2": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Acute_myeloid_leukemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_specified": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|TERT-related_disorder|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|not_specified|not_provided": 1,
    "Interstitial_lung_disease_2|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Dyskeratosis_congenita|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Aplastic_anemia": 2,
    "not_provided|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Dyskeratosis_congenita": 12,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Pulmonary_fibrosis": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Idiopathic_Pulmonary_Fibrosis": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita": 1,
    "not_provided|Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|not_specified|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Dyskeratosis_congenita|Autosomal_recessive_dyskeratosis_congenita_4|Dyskeratosis_congenita|_autosomal_recessive_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "TERT-related_disorder|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Aplastic_anemia|TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_1|Acute_myeloid_leukemia|Interstitial_lung_disease_2": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis|TERT-related_disorder|not_provided|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|TERT-related_disorder|Dyskeratosis_congenita": 1,
    "TERT-related_disorder|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Intellectual_disability": 1,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5": 82,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|not_specified|not_provided|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_provided|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis|not_specified": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Pulmonary_fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Interstitial_lung_disease_2": 1,
    "Dyskeratosis_congenita|not_specified|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|not_specified|Dyskeratosis_congenita": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|not_provided|Dyskeratosis_congenita": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|not_specified|TERT-related_disorder": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|not_specified|not_provided|Dyskeratosis_congenita|Interstitial_lung_disease_2|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided": 1,
    "not_specified|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita": 2,
    "not_specified|Dyskeratosis_congenita|TERT-related_disorder|not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2": 2,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita|Autosomal_recessive_dyskeratosis_congenita_4|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Acute_myeloid_leukemia|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "not_specified|not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis|not_specified|not_provided": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 3,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_provided": 1,
    "not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis": 1,
    "Hoyeraal-Hreidarsson_syndrome|Autosomal_recessive_dyskeratosis_congenita_4|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Telomere_syndrome|Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_2|Acute_myeloid_leukemia|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Interstitial_lung_disease_2|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Myelodysplasia|not_provided|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_specified|not_provided|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Interstitial_lung_disease_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia": 1,
    "Chronic_osteomyelitis|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Aplastic_anemia": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Dyskeratosis_congenita": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|not_specified|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Chronic_diarrhea|Chronic_obstructive_pulmonary_disease|Immunodeficiency|Decreased_circulating_immunoglobulin_concentration|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder|Dyskeratosis_congenita|not_specified": 1,
    "not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis": 1,
    "Telomere_syndrome|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Acute_myeloid_leukemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Acute_myeloid_leukemia|Aplastic_anemia": 2,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|not_specified|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder": 3,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_provided|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Acute_myeloid_leukemia|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 2,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|TERT-related_disorder": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Dyskeratosis_congenita|TERT-related_disorder": 1,
    "Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|not_provided|not_specified|Dyskeratosis_congenita": 1,
    "Combined_pulmonary_fibrosis-emphysema_syndrome|Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Chronic_osteomyelitis|Chronic_obstructive_pulmonary_disease|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Interstitial_lung_disease_2": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_specified|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Idiopathic_Pulmonary_Fibrosis": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Interstitial_lung_disease_2": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|TERT-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Interstitial_lung_disease_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Dyskeratosis_congenita": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "not_specified|Inherited_Immunodeficiency_Diseases": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Dyskeratosis_congenita": 1,
    "TERT-related_disorder|Dyskeratosis_Congenita|_Recessive|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_specified|not_provided|Dyskeratosis_congenita|Interstitial_lung_disease_2|Hepatoblastoma|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|not_specified|Interstitial_lung_disease_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_1|Acute_myeloid_leukemia|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita": 3,
    "Dyskeratosis_congenita|TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|not_specified|not_provided|Dyskeratosis_congenita|Autosomal_recessive_dyskeratosis_congenita_4|Aplastic_anemia": 1,
    "Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis": 1,
    "Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified": 2,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Interstitial_lung_disease_2|Aplastic_anemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_1|Acute_myeloid_leukemia|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_1|Acute_myeloid_leukemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_2|Interstitial_lung_disease_2|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis": 3,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Interstitial_lung_disease_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|Interstitial_lung_disease_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_1|Acute_myeloid_leukemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|not_provided|not_specified|Dyskeratosis_congenita|Hepatocellular_carcinoma": 1,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|TERT-related_disorder|Dyskeratosis_congenita|Interstitial_lung_disease_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|not_specified|not_provided|Dyskeratosis_congenita|Acute_myeloid_leukemia|Interstitial_lung_disease_2": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia|Malignant_tumor_of_breast": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Interstitial_lung_disease_2|Aplastic_anemia|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Acute_myeloid_leukemia": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|not_provided|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Interstitial_lung_disease_2": 1,
    "not_specified|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|not_provided|Dyskeratosis_congenita|Aplastic_anemia": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Hepatocellular_carcinoma": 2,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Acute_myeloid_leukemia|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Idiopathic_Pulmonary_Fibrosis|not_specified|Aplastic_anemia|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Dyskeratosis_congenita|Idiopathic_Pulmonary_Fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-associated_disorder|not_provided": 1,
    "TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_specified|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia": 1,
    "TERT-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Acute_myeloid_leukemia|Interstitial_lung_disease_2|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita": 1,
    "Intellectual_disability|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Acute_myeloid_leukemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis|not_provided|Interstitial_lung_disease_2": 1,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Dyskeratosis_congenita|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9": 1,
    "Abnormal_pulmonary_interstitial_morphology|Short_telomere_length|not_provided": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Aplastic_anemia|Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Pulmonary_fibrosis": 1,
    "Telomere_syndrome": 3,
    "TERT-related_disorder|not_provided": 1,
    "Pulmonary_fibrosis|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Abnormal_pulmonary_interstitial_morphology": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Intellectual_disability|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Idiopathic_Pulmonary_Fibrosis|not_specified|Aplastic_anemia|TERT-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Interstitial_lung_disease_2": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Pulmonary_fibrosis|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_2|Idiopathic_Pulmonary_Fibrosis|Aplastic_anemia": 1,
    "TERT-related_disorder|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|Aplastic_anemia|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Interstitial_lung_disease_2|Acute_myeloid_leukemia|not_provided|Dyskeratosis_congenita": 1,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|TERT-related_disorder|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|Dyskeratosis_congenita|_autosomal_dominant_1|Acute_myeloid_leukemia|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|_autosomal_dominant_2|Interstitial_lung_disease_2|Aplastic_anemia|Idiopathic_Pulmonary_Fibrosis": 1,
    "Pulmonary_fibrosis|Interstitial_lung_disease_2": 3,
    "Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_9|Dyskeratosis_congenita|Malignant_tumor_of_urinary_bladder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_provided|Malignant_tumor_of_urinary_bladder|not_specified": 1,
    "Lung_sarcomatoid_carcinoma": 3,
    "not_specified|Idiopathic_Pulmonary_Fibrosis|Dyskeratosis_congenita|_autosomal_dominant_2|not_provided": 1,
    "Coronary_artery_disease|_susceptibility_to|Chronic_osteomyelitis": 1,
    "CLPTM1L-related_disorder": 19,
    "Nicotine_dependence|_protection_against": 1,
    "Classic_dopamine_transporter_deficiency_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Parkinsonism-dystonia|_infantile": 1,
    "Classic_dopamine_transporter_deficiency_syndrome": 16,
    "Parkinsonism-dystonia|_infantile": 290,
    "Parkinsonism-dystonia|_infantile|not_provided": 11,
    "Parkinsonism-dystonia|_infantile|Inborn_genetic_diseases|not_provided": 3,
    "Tobacco_addiction|_susceptibility_to|Classic_dopamine_transporter_deficiency_syndrome|Parkinsonism-dystonia|_infantile": 1,
    "SLC6A3-related_disorder": 2,
    "not_provided|Parkinsonism-dystonia|_infantile": 16,
    "not_provided|Parkinsonism-dystonia|_infantile|Inborn_genetic_diseases": 1,
    "Parkinsonism-dystonia|_infantile|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Parkinsonism-dystonia|_infantile": 7,
    "not_provided|not_specified|Parkinsonism-dystonia|_infantile": 1,
    "Classic_dopamine_transporter_deficiency_syndrome|Tobacco_addiction|_susceptibility_to|SLC6A3-related_disorder|not_provided|Parkinsonism-dystonia|_infantile": 1,
    "Parkinsonism-dystonia|_infantile|Inborn_genetic_diseases|not_provided|Classic_dopamine_transporter_deficiency_syndrome|See_cases": 1,
    "SLC6A3-related_disorder|not_provided": 1,
    "Parkinsonism-dystonia|_infantile|Inborn_genetic_diseases": 5,
    "Parkinsonism-dystonia|_infantile|Classic_dopamine_transporter_deficiency_syndrome|Tobacco_addiction|_susceptibility_to": 1,
    "Parkinsonism-dystonia|_infantile|Classic_dopamine_transporter_deficiency_syndrome": 4,
    "Parkinsonism-dystonia|_infantile|not_specified": 1,
    "not_provided|Parkinsonism-dystonia|_infantile|SLC6A3-related_disorder": 2,
    "Parkinsonism-dystonia|_infantile|not_provided|Classic_dopamine_transporter_deficiency_syndrome": 1,
    "not_provided|SLC6A3-related_disorder|Parkinsonism-dystonia|_infantile|Tobacco_addiction|_susceptibility_to|Classic_dopamine_transporter_deficiency_syndrome": 1,
    "not_provided|SLC6A3-related_disorder|Parkinsonism-dystonia|_infantile": 2,
    "Parkinsonism-dystonia|_infantile|Classic_dopamine_transporter_deficiency_syndrome|not_provided": 1,
    "Classic_dopamine_transporter_deficiency_syndrome|Parkinsonism-dystonia|_infantile|not_provided|not_specified": 1,
    "not_provided|Parkinsonism-dystonia|_infantile|Inborn_genetic_diseases|Tobacco_addiction|_susceptibility_to|Classic_dopamine_transporter_deficiency_syndrome": 1,
    "Gait_imbalance|Difficulty_walking|Dysphagia|Irritability|Delayed_speech_and_language_development|Limb_dystonia": 1,
    "not_provided|Parkinsonism-dystonia|_infantile|Tobacco_addiction|_susceptibility_to|Classic_dopamine_transporter_deficiency_syndrome": 1,
    "Parkinsonism-dystonia|_infantile|SLC6A3-related_disorder": 1,
    "Classic_dopamine_transporter_deficiency_syndrome|Parkinsonism-dystonia|_infantile": 1,
    "Parkinsonism-dystonia|_infantile|Tobacco_addiction|_susceptibility_to|Classic_dopamine_transporter_deficiency_syndrome|not_provided": 1,
    "Parkinsonism-dystonia|_infantile|Tobacco_addiction|_susceptibility_to|Classic_dopamine_transporter_deficiency_syndrome": 3,
    "Classic_dopamine_transporter_deficiency_syndrome|Parkinsonism-dystonia|_infantile|not_provided": 1,
    "Parkinsonism-dystonia|_infantile|not_provided|Classic_dopamine_transporter_deficiency_syndrome|SLC6A3-related_disorder|Tobacco_addiction|_susceptibility_to": 1,
    "SLC6A3-related_disorder|Parkinsonism-dystonia|_infantile|not_provided": 1,
    "not_provided|Classic_dopamine_transporter_deficiency_syndrome|Parkinsonism-dystonia|_infantile": 1,
    "not_specified|Parkinsonism-dystonia|_infantile": 1,
    "Classic_dopamine_transporter_deficiency_syndrome|not_provided|Parkinsonism-dystonia|_infantile": 2,
    "not_provided|Parkinsonism-dystonia|_infantile|Classic_dopamine_transporter_deficiency_syndrome": 1,
    "Parkinsonism-dystonia|_infantile|not_provided|Inborn_genetic_diseases": 1,
    "Classic_dopamine_transporter_deficiency_syndrome|Tobacco_addiction|_susceptibility_to|Parkinsonism-dystonia|_infantile": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_9|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified": 1,
    "NDUFS6-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_9|not_provided": 8,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_9": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Mitochondrial_complex_I_deficiency": 2,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_9": 10,
    "not_provided|Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_9": 12,
    "Mitochondrial_complex_I_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_9|not_specified": 1,
    "not_provided|NDUFS6-related_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_9|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|IRX1-related_disorder": 3,
    "IRX1-related_disorder": 7,
    "ICE1-related_disorder": 4,
    "not_provided|ICE1-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_5": 55,
    "Intellectual_disability|_autosomal_recessive_5|not_provided": 6,
    "not_specified|Intellectual_disability|_autosomal_recessive_5": 1,
    "NSUN2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_5": 1,
    "Intellectual_disability|_autosomal_recessive_5|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_5|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_5": 2,
    "not_provided|NSUN2-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|Intellectual_disability|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|Intellectual_disability|_autosomal_recessive_5": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_5|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_5|NSUN2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_5": 3,
    "not_provided|Intellectual_disability|_autosomal_recessive_5": 4,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_5": 3,
    "not_provided|Intellectual_disability|_autosomal_recessive_5|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_5|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_5|NSUN2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_5|Inborn_genetic_diseases": 1,
    "Intellectual_Disability|_Recessive|not_provided|Intellectual_disability|_autosomal_recessive_5": 1,
    "Phenylketonuria|Intellectual_disability|_autosomal_recessive_5": 1,
    "Intellectual_disability|_autosomal_recessive_5|not_specified|not_provided": 2,
    "not_provided|not_specified|Intellectual_disability|_autosomal_recessive_5|Intellectual_disability": 1,
    "Autosomal_recessive_non-syndromic_intellectual_disability|Intellectual_disability|_autosomal_recessive_5|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_5|Intellectual_disability|Phenylketonuria": 1,
    "not_specified|not_provided|NSUN2-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_non-syndromic_intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_recessive_5": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|Intellectual_disability|_autosomal_recessive_5": 1,
    "Intellectual_disability|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|NSUN2-related_disorder|Intellectual_disability|_autosomal_recessive_5": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_5|NSUN2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_5|not_provided": 1,
    "NSUN2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_5|NSUN2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|NSUN2-related_disorder|not_specified|Intellectual_disability|_autosomal_recessive_5|not_provided": 1,
    "Intellectual_Disability|_Recessive|not_provided": 18,
    "ADCY2-related_disorder": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|not_specified|Methylcobalamin_deficiency_type_cblE": 1,
    "MTRR-related_disorder": 2,
    "not_provided|Methylcobalamin_deficiency_type_cblE": 11,
    "not_provided|Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblE|not_specified": 8,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE": 22,
    "Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism|MTRR-related_disorder": 1,
    "Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive": 21,
    "Methylcobalamin_deficiency_type_cblE|not_provided": 5,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Gastrointestinal_stromal_tumor|Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|_susceptibility_to|Down_syndrome|_susceptibility_to|Methotrexate_response": 1,
    "Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE": 11,
    "not_specified|Methylcobalamin_deficiency_type_cblE": 10,
    "Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|not_provided": 1,
    "not_specified|Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism": 2,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE": 6,
    "Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism": 7,
    "MTRR-related_disorder|not_provided|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE": 1,
    "not_provided|Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE": 3,
    "Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE|Homocystinuria_without_methylmalonic_aciduria": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylcobalamin_deficiency_type_cblE|Inborn_genetic_diseases": 1,
    "MTRR-related_disorder|Methylcobalamin_deficiency_type_cblE": 1,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism": 2,
    "Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblE|MTRR-related_disorder": 3,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|not_specified|Gastrointestinal_stromal_tumor|Methylcobalamin_deficiency_type_cblE": 1,
    "Methylcobalamin_deficiency_type_cblE|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 2,
    "Methylcobalamin_deficiency_type_cblE|Inborn_genetic_diseases": 7,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Inborn_genetic_diseases": 2,
    "not_provided|Methylcobalamin_deficiency_type_cblE|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|MTRR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided": 4,
    "Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblG": 1,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_specified|not_provided|Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism": 3,
    "not_provided|Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE": 1,
    "Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive|Inborn_genetic_diseases": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Gastrointestinal_stromal_tumor|Methylcobalamin_deficiency_type_cblE": 2,
    "Methylcobalamin_deficiency_type_cblE|not_provided|not_specified|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism|Neural_tube_defects|_folate-sensitive|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE|not_provided": 1,
    "MTRR-related_disorder|Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE|not_specified|not_provided|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE": 1,
    "Methylcobalamin_deficiency_type_cblE|not_specified|not_provided": 2,
    "Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE|not_provided|Inborn_genetic_diseases": 1,
    "Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|not_specified": 1,
    "Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive": 1,
    "MTRR-related_disorder|Methylcobalamin_deficiency_type_cblE|not_provided": 1,
    "Neural_tube_defects|_folate-sensitive|Methylcobalamin_deficiency_type_cblE|not_provided": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|not_provided|Methylcobalamin_deficiency_type_cblE": 1,
    "Methylcobalamin_deficiency_type_cblE|not_provided|MTRR-related_disorder": 1,
    "MTRR-related_disorder|Neural_tube_defects|_folate-sensitive|Inborn_genetic_diseases|not_provided|Methylcobalamin_deficiency_type_cblE": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylcobalamin_deficiency_type_cblE|not_specified|not_provided": 1,
    "not_provided|Methylcobalamin_deficiency_type_cblE|Neural_tube_defects|_folate-sensitive": 1,
    "not_specified|MTRR-related_disorder|Methylcobalamin_deficiency_type_cblE|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|not_specified|Methylcobalamin_deficiency_type_cblE": 1,
    "Neural_tube_defects|_folate-sensitive|Inborn_genetic_diseases": 1,
    "MTRR-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylcobalamin_deficiency_type_cblE": 1,
    "not_provided|Inborn_genetic_diseases|Methylcobalamin_deficiency_type_cblE": 1,
    "not_provided|SEMA5A-related_disorder": 4,
    "SEMA5A-related_disorder|not_provided": 6,
    "SEMA5A-related_disorder": 13,
    "not_specified|not_provided|SEMA5A-related_disorder": 1,
    "SEMA5A-related_disorder|not_specified": 1,
    "SEMA5A-associated_Neurodevelopmental_syndrome": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia": 216,
    "Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia|not_specified|not_provided": 6,
    "Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia|not_specified": 9,
    "Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia|CCT5-related_disorder": 6,
    "Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia|not_provided": 15,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia": 17,
    "Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia|not_provided|CCT5-related_disorder": 2,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia": 12,
    "Hereditary_spastic_paraplegia|Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia|not_provided": 1,
    "Sensory_Neuropathy_with_Spastic_Paraplegia|Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia": 1,
    "CCT5-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_with_spastic_paraplegia": 1,
    "Sensory_Neuropathy_with_Spastic_Paraplegia": 6,
    "Epilepsy|_familial_adult_myoclonic|_3": 5,
    "MARCHF6-related_disorder": 1,
    "CTNND2-related_disorder": 13,
    "CTNND2-related_disorder|not_provided": 6,
    "not_provided|CTNND2-related_disorder": 8,
    "CTNND2-associated_Neurodevelopmental_syndrome": 2,
    "CTNND2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|CTNND2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CTNND2-related_disorder": 1,
    "Primary_ciliary_dyskinesia_3|not_provided": 9,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 221,
    "Primary_ciliary_dyskinesia_3|not_provided|Primary_ciliary_dyskinesia": 10,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 114,
    "Primary_ciliary_dyskinesia_3|not_specified|not_provided": 9,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_3": 15,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 9,
    "not_provided|Primary_ciliary_dyskinesia_3|not_specified": 3,
    "Primary_ciliary_dyskinesia_3|Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_specified": 3,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_3": 3,
    "Primary_ciliary_dyskinesia|DNAH5-related_disorder|not_provided|Primary_ciliary_dyskinesia_3": 3,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_provided": 10,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 33,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 45,
    "DNAH5-related_disorder": 23,
    "not_provided|Primary_ciliary_dyskinesia_3|not_specified|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia|DNAH5-related_disorder": 29,
    "not_specified|Primary_ciliary_dyskinesia_3|not_provided|Primary_ciliary_dyskinesia": 2,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia": 12,
    "not_provided|Primary_ciliary_dyskinesia_3": 13,
    "not_provided|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 11,
    "Primary_ciliary_dyskinesia|DNAH5-related_disorder|Primary_ciliary_dyskinesia_3": 4,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_3": 12,
    "Primary_ciliary_dyskinesia_3|not_specified|Primary_ciliary_dyskinesia": 8,
    "Primary_ciliary_dyskinesia|Infertility_disorder|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_specified": 10,
    "Primary_ciliary_dyskinesia|DNAH5-related_disorder|not_provided": 4,
    "not_specified|Primary_ciliary_dyskinesia_3|not_provided": 3,
    "not_specified|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 6,
    "Heterotaxy|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_3|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_3": 2,
    "Primary_ciliary_dyskinesia_3|not_provided|not_specified": 3,
    "not_specified|Primary_ciliary_dyskinesia|DNAH5-related_disorder|not_provided|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_3|not_provided|Primary_ciliary_dyskinesia|Situs_inversus": 1,
    "DNAH5-related_disorder|not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 2,
    "DNAH5-related_disorder|not_provided|Primary_ciliary_dyskinesia": 3,
    "not_provided|Primary_ciliary_dyskinesia_3|DNAH5-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_3|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia|not_provided": 3,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|not_provided": 9,
    "Primary_ciliary_dyskinesia|Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided|Primary_ciliary_dyskinesia_3": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia": 3,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 4,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 8,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|not_specified": 1,
    "Glycine_encephalopathy_1|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_provided|See_cases": 1,
    "not_specified|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia": 1,
    "DNAH5-related_disorder|not_specified|Primary_ciliary_dyskinesia": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 1,
    "DNAH5-related_disorder|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 3,
    "Primary_ciliary_dyskinesia|Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided": 1,
    "not_provided|DNAH5-related_disorder|Primary_ciliary_dyskinesia": 1,
    "not_provided|Heterotaxy|Primary_ciliary_dyskinesia": 1,
    "DNAH5-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 1,
    "not_provided|Primary_ciliary_dyskinesia|DNAH5-related_disorder": 2,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 8,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_3|DNAH5-related_disorder": 2,
    "DNAH5-related_disorder|not_provided|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 1,
    "not_provided|DNAH5-related_disorder|Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia": 1,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia_3|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_3|DNAH5-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|Infertility_disorder|not_provided": 1,
    "Primary_ciliary_dyskinesia|not_provided|DNAH5-related_disorder": 2,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_provided": 2,
    "not_specified|Primary_ciliary_dyskinesia|not_provided": 25,
    "Primary_ciliary_dyskinesia|not_provided|not_specified|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia": 101,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|Situs_inversus": 1,
    "Primary_ciliary_dyskinesia|not_specified|DNAH5-related_disorder": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|Male_infertility": 1,
    "DNAH5-related_disorder|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_3": 1,
    "not_provided|Infertility_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3": 1,
    "not_provided|DNAH5-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_provided|not_specified": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_3|not_provided|Primary_ciliary_dyskinesia|DNAH5-related_disorder": 1,
    "Primary_ciliary_dyskinesia_3|DNAH5-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Kartagener_syndrome": 25,
    "Primary_ciliary_dyskinesia_3|not_provided|not_specified|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome|Primary_ciliary_dyskinesia_3": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia|DNAH5-related_disorder|not_specified": 1,
    "not_provided|Primary_ciliary_dyskinesia|DNAH5-related_disorder|Primary_ciliary_dyskinesia_3": 1,
    "Primary_Ciliary_Dyskinesia_(DNAH5-related)": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|DNAH5-related_disorder|not_provided": 1,
    "Primary_ciliary_dyskinesia|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia|not_provided|not_specified": 10,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_3|not_specified": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_3|not_provided": 1,
    "Primary_ciliary_dyskinesia_3|not_specified": 1,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|not_provided": 1,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|DNAH5-related_disorder": 1,
    "Primary_ciliary_dyskinesia_3|Primary_ciliary_dyskinesia|not_provided|DNAH5-related_disorder": 1,
    "not_specified|Primary_ciliary_dyskinesia_3": 1,
    "Inborn_genetic_diseases|not_provided|TRIO-related_disorder": 3,
    "TRIO-related_disorder|not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Inborn_genetic_diseases": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 19,
    "TRIO-related_disorder|not_provided": 18,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 16,
    "TRIO-related_disorder|not_provided|not_specified": 2,
    "TRIO-related_disorder": 70,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 108,
    "not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 7,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 7,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|not_provided": 12,
    "Inborn_genetic_diseases|TRIO-related_disorder": 8,
    "not_provided|Inborn_genetic_diseases|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 2,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|not_provided": 3,
    "not_provided|TRIO-related_disorder": 21,
    "not_provided|Developmental_delay|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 2,
    "not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 4,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Inborn_genetic_diseases|not_provided|Intellectual_disability|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|TRIO-related_disorder|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 11,
    "not_provided|TRIO-related_disorder|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|not_specified": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|not_provided": 5,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Inborn_genetic_diseases": 2,
    "TRIO-related_disorder|not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "TRIO-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Intellectual_disability": 1,
    "TRIO-related_disorder|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|not_provided|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|not_provided|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "not_specified|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "Hereditary_ataxia|not_provided|Inborn_genetic_diseases": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|not_provided": 1,
    "TRIO-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "Intellectual_disability|See_cases|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "TRIO-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|TRIO-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|TRIO-related_disorder|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome": 1,
    "not_specified|TRIO-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|TRIO-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|TRIO-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "not_specified|not_provided|Intellectual_disability": 6,
    "Inborn_genetic_diseases|not_provided|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "Tip-toe_gait|not_provided|TRIO-related_disorder": 1,
    "not_provided|TRIO-related_disorder|Inborn_genetic_diseases|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|not_specified|Inborn_genetic_diseases": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|Inborn_genetic_diseases|not_provided": 1,
    "TRIO-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|TRIO-related_disorder|Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly": 1,
    "TRIO-related_disorder|Intellectual_disability|_autosomal_dominant_40|Inborn_genetic_diseases|not_provided": 1,
    "TRIO-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Micrognathia-recurrent_infections-behavioral_abnormalities-mild_intellectual_disability_syndrome|Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_63|_with_macrocephaly|not_provided|Inborn_genetic_diseases": 1,
    "OTULIN-related_disorder": 2,
    "not_provided|OTULIN-related_disorder": 5,
    "not_specified|Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_recessive|not_provided": 1,
    "Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_recessive": 10,
    "not_provided|Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_recessive": 2,
    "Immunodeficiency_107|_susceptibility_to_invasive_staphylococcus_aureus_infection": 4,
    "OTULIN-related_disorder|not_provided": 1,
    "Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_recessive|not_provided": 1,
    "Immunodeficiency_107|_susceptibility_to_invasive_staphylococcus_aureus_infection|Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_recessive": 2,
    "OTULIN-related_disorder|not_specified": 1,
    "not_specified|OTULIN-related_disorder|not_provided": 1,
    "Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_dominant": 1,
    "Autoinflammation|_panniculitis|_and_dermatosis_syndrome|_autosomal_recessive|Immunodeficiency_107|_susceptibility_to_invasive_staphylococcus_aureus_infection|not_provided": 1,
    "Craniometaphyseal_dysplasia|_autosomal_dominant|Chondrocalcinosis_2": 42,
    "Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant": 96,
    "not_provided|Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant": 20,
    "Chondrocalcinosis|Craniometadiaphyseal_dysplasia_wormian_bone_type": 17,
    "not_provided|Craniometadiaphyseal_dysplasia_wormian_bone_type|Chondrocalcinosis": 1,
    "not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|Chondrocalcinosis_2": 19,
    "Craniometadiaphyseal_dysplasia_wormian_bone_type|Chondrocalcinosis|not_provided": 2,
    "Craniometaphyseal_dysplasia|_autosomal_dominant|not_provided|Chondrocalcinosis_2": 5,
    "Craniometadiaphyseal_dysplasia_wormian_bone_type|Chondrocalcinosis": 6,
    "Craniometadiaphyseal_dysplasia_wormian_bone_type|not_provided|Chondrocalcinosis": 2,
    "ANKH-related_disorder": 2,
    "CHONDROCALCINOSIS_2|_SPORADIC": 1,
    "not_provided|ANKH-related_disorder": 4,
    "ANKH-related_disorder|Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant|not_provided": 1,
    "Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant|not_provided": 1,
    "ANKH-related_disorder|not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|Chondrocalcinosis_2": 2,
    "not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|ANKH-related_disorder": 1,
    "Craniometaphyseal_dysplasia|_autosomal_dominant": 6,
    "ANKH-related_disorder|Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant|not_specified|not_provided": 1,
    "not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant": 6,
    "not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|Inborn_genetic_diseases|Chondrocalcinosis_2": 1,
    "not_provided|ANKH-related_disorder|Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant": 1,
    "not_provided|Inborn_genetic_diseases|Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant": 1,
    "ANKH-related_disorder|Craniometaphyseal_dysplasia|_autosomal_dominant|not_provided": 1,
    "Chondrocalcinosis_2": 2,
    "Inborn_genetic_diseases|Chondrocalcinosis_2|Craniometaphyseal_dysplasia|_autosomal_dominant": 1,
    "Chondrocalcinosis_2|not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant": 2,
    "ANKH-related_disorder|not_specified|Chondrocalcinosis_2|not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant": 1,
    "not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|ANKH-related_disorder|Chondrocalcinosis_2": 1,
    "not_specified|not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|Chondrocalcinosis_2": 1,
    "not_provided|Chondrocalcinosis_2": 1,
    "Chondrocalcinosis_2|not_provided": 1,
    "ANKH-related_disorder|Chondrocalcinosis_2": 1,
    "Benign_familial_infantile_epilepsy|Chondrocalcinosis_2": 1,
    "Chondrocalcinosis|not_provided|Craniometaphyseal_dysplasia|_autosomal_dominant|Craniometadiaphyseal_dysplasia_wormian_bone_type": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 31,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 8,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided": 7,
    "Hereditary_sensory_and_autonomic_neuropathy_type_2": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_2|not_provided": 2,
    "not_provided|RETREG1-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 5,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided": 3,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_specified|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_2": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|Hereditary_sensory_and_autonomic_neuropathy_type_2": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_2|Charcot-Marie-Tooth_disease": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_2": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided|not_specified": 2,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 6,
    "not_provided|Inborn_genetic_diseases|RETREG1-related_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_2|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|not_provided|not_specified": 2,
    "RETREG1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Neuropathy|_hereditary_sensory_and_autonomic|_type_2B": 1,
    "not_provided|RETREG1-related_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2B|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_2": 1,
    "CDH18-related_disorder": 2,
    "Childhood_apraxia_of_speech": 123,
    "PRDM9-related_disorder": 6,
    "CDH10-related_condition": 1,
    "not_specified|CDH10-related_condition": 1,
    "DROSHA-related_disorder": 59,
    "DROSHA-related_disorder|not_provided": 5,
    "DROSHA-related_neurodevelopmental_disorder": 1,
    "Pineoblastoma": 7,
    "not_provided|DROSHA-related_disorder": 7,
    "not_specified|DROSHA-related_disorder": 1,
    "DROSHA-related_disorder|not_specified": 2,
    "not_provided|PDZD2-related_disorder": 5,
    "PDZD2-related_disorder": 79,
    "Lissencephaly": 31,
    "not_specified|PDZD2-related_disorder": 3,
    "PDZD2-related_disorder|not_provided": 4,
    "PDZD2-related_disorder|not_specified": 1,
    "not_specified|PDZD2-related_disorder|not_provided": 1,
    "not_specified|Pure_or_complex_autosomal_recessive_spastic_paraplegia": 8,
    "Pure_or_complex_autosomal_recessive_spastic_paraplegia": 176,
    "Pure_or_complex_autosomal_recessive_spastic_paraplegia|not_specified": 9,
    "ZFR-related_disorder": 6,
    "not_provided|Pure_or_complex_autosomal_recessive_spastic_paraplegia": 7,
    "Pure_or_complex_autosomal_recessive_spastic_paraplegia|not_provided|ZFR-related_disorder": 1,
    "Pure_or_complex_autosomal_recessive_spastic_paraplegia|ZFR-related_disorder": 3,
    "NPR3-related_disorder": 4,
    "not_provided|NPR3-related_disorder": 2,
    "Boudin-Mortier_syndrome": 6,
    "NPR3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|NPR3-related_disorder|not_provided": 1,
    "Trichothiodystrophy_7|_nonphotosensitive|TARS1-related_disorder|not_provided": 1,
    "TARS1-related_disorder": 12,
    "not_provided|TARS1-related_disorder": 4,
    "TARS1-related_disorder|not_provided": 2,
    "Trichothiodystrophy": 3,
    "Trichothiodystrophy_7|_nonphotosensitive": 4,
    "not_specified|TARS1-related_disorder": 2,
    "not_provided|Trichothiodystrophy_7|_nonphotosensitive": 2,
    "not_provided|TARS1-related_disorder|Trichothiodystrophy_7|_nonphotosensitive": 1,
    "Oculocutaneous_albinism": 21,
    "not_provided|Oculocutaneous_albinism_type_4": 21,
    "Oculocutaneous_albinism_type_4": 33,
    "not_provided|Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 4,
    "SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|Oculocutaneous_albinism_type_4|not_provided": 7,
    "Oculocutaneous_albinism_type_4|not_provided|SLC45A2-related_disorder": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|not_provided": 2,
    "Oculocutaneous_albinism_type_4|not_provided": 18,
    "Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|SLC45A2-related_disorder|not_provided|not_specified": 1,
    "Abnormal_bleeding|Thrombocytopenia|not_provided|Oculocutaneous_albinism_type_4": 1,
    "not_specified|not_provided|Oculocutaneous_albinism_type_4": 1,
    "Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|SLC45A2-related_disorder": 1,
    "not_specified|Oculocutaneous_albinism_type_4": 2,
    "not_specified|Oculocutaneous_albinism_type_4|not_provided": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|Oculocutaneous_albinism_type_4|not_specified|not_provided": 1,
    "Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 7,
    "Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|not_provided": 3,
    "SLC45A2-related_disorder|not_provided|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|Oculocutaneous_albinism_type_4": 1,
    "not_provided|SLC45A2-related_disorder|not_specified": 1,
    "SLC45A2-related_disorder": 5,
    "not_provided|Malignant_melanoma_of_skin|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 1,
    "not_specified|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|Oculocutaneous_albinism_type_4|not_provided": 1,
    "Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|SLC45A2-related_disorder|not_provided": 1,
    "Oculocutaneous_albinism|not_provided|Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|Oculocutaneous_albinism_type_4": 3,
    "not_specified|not_provided|Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 1,
    "SLC45A2-related_disorder|not_provided|Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR": 2,
    "not_provided|SLC45A2-related_disorder": 1,
    "Albinism_or_congenital_nystagmus|SLC45A2-related_disorder|not_provided|Oculocutaneous_albinism_type_4|Inborn_genetic_diseases": 1,
    "not_provided|Oculocutaneous_albinism_type_4|SLC45A2-related_disorder": 1,
    "Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|SLC45A2-related_disorder": 1,
    "Inborn_genetic_diseases|SLC45A2-related_disorder|not_provided|Oculocutaneous_albinism_type_4": 1,
    "SLC45A2-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|Oculocutaneous_albinism_type_4|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_4|SKIN/HAIR/EYE_PIGMENTATION_5|_BLACK/NONBLACK_HAIR|SLC45A2-related_disorder": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency": 268,
    "Alpha-methylacyl-CoA_racemase_deficiency|Oculocutaneous_albinism": 1,
    "not_provided|Oculocutaneous_albinism|Alpha-methylacyl-CoA_racemase_deficiency": 5,
    "not_provided|Alpha-methylacyl-CoA_racemase_deficiency": 8,
    "Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|not_provided": 11,
    "not_provided|Oculocutaneous_albinism|Congenital_bile_acid_synthesis_defect_4|Alpha-methylacyl-CoA_racemase_deficiency": 2,
    "not_provided|AMACR-related_disorder|Alpha-methylacyl-CoA_racemase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Alpha-methylacyl-CoA_racemase_deficiency": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|Inborn_genetic_diseases": 11,
    "Alpha-methylacyl-CoA_racemase_deficiency|AMACR-related_disorder": 8,
    "AMACR-related_disorder": 11,
    "not_provided|Alpha-methylacyl-CoA_racemase_deficiency|AMACR-related_disorder": 3,
    "Inborn_genetic_diseases|Alpha-methylacyl-CoA_racemase_deficiency": 15,
    "not_provided|not_specified|Alpha-methylacyl-CoA_racemase_deficiency": 3,
    "AMACR-related_disorder|Alpha-methylacyl-CoA_racemase_deficiency": 2,
    "Inborn_genetic_diseases|Congenital_bile_acid_synthesis_defect_4|Alpha-methylacyl-CoA_racemase_deficiency|AMACR-related_disorder": 1,
    "AMACR-related_disorder|Congenital_bile_acid_synthesis_defect_4|Alpha-methylacyl-CoA_racemase_deficiency|not_specified|Mitochondrial_complex_I_deficiency": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|not_specified|not_provided": 3,
    "Oculocutaneous_albinism|Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4|not_specified|not_provided": 1,
    "Congenital_bile_acid_synthesis_defect_4|Alpha-methylacyl-CoA_racemase_deficiency|Inborn_genetic_diseases|AMACR-related_disorder|not_provided": 1,
    "not_specified|Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4|not_provided": 2,
    "AMACR-related_disorder|not_provided|Alpha-methylacyl-CoA_racemase_deficiency": 3,
    "Alpha-methylacyl-CoA_racemase_deficiency|not_specified": 1,
    "not_specified|Alpha-methylacyl-CoA_racemase_deficiency": 1,
    "not_provided|Alpha-methylacyl-CoA_racemase_deficiency|not_specified": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|AMACR-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Alpha-methylacyl-CoA_racemase_deficiency": 1,
    "AMACR-related_disorder|not_provided": 1,
    "not_provided|Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4|not_specified": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_4|Alpha-methylacyl-CoA_racemase_deficiency|not_specified": 1,
    "not_provided|Alpha-methylacyl-CoA_racemase_deficiency|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_bile_acid_synthesis_defect_4": 1,
    "not_provided|Inborn_genetic_diseases|Alpha-methylacyl-CoA_racemase_deficiency|AMACR-related_disorder": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Alpha-methylacyl-CoA_racemase_deficiency|not_provided|not_specified": 1,
    "not_provided|Alpha-methylacyl-CoA_racemase_deficiency|Inborn_genetic_diseases|Congenital_bile_acid_synthesis_defect_4": 1,
    "AMACR-related_disorder|Inborn_genetic_diseases|not_provided|Alpha-methylacyl-CoA_racemase_deficiency|Congenital_bile_acid_synthesis_defect_4": 1,
    "AMACR-related_disorder|not_provided|Alpha-methylacyl-CoA_racemase_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|AMACR-related_disorder|Alpha-methylacyl-CoA_racemase_deficiency": 1,
    "not_specified|not_provided|Alpha-methylacyl-CoA_racemase_deficiency": 1,
    "RAD1-related_disorder": 12,
    "not_specified|RAD1-related_disorder": 1,
    "RAD1-related_disorder|not_specified": 2,
    "DNAJC21-related_disorder": 4,
    "DNAJC21-related_disorder|not_provided": 7,
    "Bone_marrow_failure_syndrome_3|Inherited_bone_marrow_failure_syndrome": 2,
    "Inborn_genetic_diseases|Bone_marrow_failure_syndrome_3": 2,
    "not_provided|Bone_marrow_failure_syndrome_3": 6,
    "DNAJC21-related_disorder|Bone_marrow_failure_syndrome_3|not_provided": 1,
    "not_provided|DNAJC21-related_disorder|not_specified": 3,
    "Bone_marrow_failure_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "Bone_marrow_failure_syndrome_3": 11,
    "DNAJC21-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|DNAJC21-related_disorder": 1,
    "not_provided|Bone_marrow_failure_syndrome_3|DNAJC21-related_disorder": 1,
    "DNAJC21-related_disorder|not_specified|not_provided": 1,
    "Inherited_bone_marrow_failure_syndrome|Bone_marrow_failure_syndrome_3|not_provided": 1,
    "Bone_marrow_failure_syndrome_3|DNAJC21-related_disorder|not_provided": 2,
    "Shwachman_syndrome": 7,
    "DNAJC21-related_disorder|not_specified|Bone_marrow_failure_syndrome_3|not_provided": 1,
    "Bone_marrow_failure_syndrome_3|not_provided": 3,
    "DNAJC21-related_disorder|Bone_marrow_failure_syndrome_3|Shwachman-Diamond_syndrome_1|not_provided": 1,
    "not_provided|DNAJC21-related_disorder": 2,
    "Bone_marrow_failure_syndrome_3|not_provided|Inborn_genetic_diseases": 1,
    "Bone_marrow_failure_syndrome_3|Inherited_bone_marrow_failure_syndrome|not_provided|Shwachman-Diamond_syndrome_1": 1,
    "Inborn_genetic_diseases|Bone_marrow_failure_syndrome_3|Shwachman-Diamond_syndrome_1|not_provided": 1,
    "DNAJC21-related_disorder|not_provided|Bone_marrow_failure_syndrome_3|not_specified": 1,
    "Bone_marrow_failure_syndrome_3|not_provided|not_specified|Shwachman-Diamond_syndrome_1|Inborn_genetic_diseases": 1,
    "not_specified|DNAJC21-related_disorder|not_provided": 1,
    "Shwachman-Diamond_syndrome_1|Bone_marrow_failure_syndrome_3|not_provided": 1,
    "Bone_marrow_failure_syndrome_3|not_provided|Shwachman-Diamond_syndrome_1": 1,
    "Inborn_genetic_diseases|DNAJC21-related_disorder|not_provided": 1,
    "Beta-aminoisobutyric_acid|_urinary_excretion_of": 2,
    "PRLR-related_disorder": 3,
    "Familial_hyperprolactinemia": 4,
    "not_specified|Multiple_fibroadenoma_of_the_breast|Familial_hyperprolactinemia": 1,
    "PRLR-related_disorder|not_provided": 1,
    "PRLR-related_disorder|Multiple_fibroadenoma_of_the_breast": 1,
    "not_specified|Familial_hyperprolactinemia|Multiple_fibroadenoma_of_the_breast": 1,
    "Multiple_fibroadenoma_of_the_breast|Familial_hyperprolactinemia": 1,
    "Spermatogenic_failure_43": 10,
    "Spermatogenic_failure_43|not_specified|not_provided": 3,
    "SPEF2-related_disorder": 4,
    "not_provided|Spermatogenic_failure_43": 3,
    "Spermatogenic_failure_43|not_provided|not_specified": 4,
    "Inborn_genetic_diseases|SPEF2-related_disorder": 3,
    "not_provided|SPEF2-related_disorder|Spermatogenic_failure_43": 1,
    "SPEF2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|SPEF2-related_disorder|not_provided": 1,
    "not_provided|SPEF2-related_disorder": 1,
    "SPEF2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Immunodeficiency_104|Severe_combined_immunodeficiency_disease": 1,
    "IMMUNODEFICIENCY_104|_SEVERE_COMBINED|_SUSCEPTIBILITY_TO|Immunodeficiency_104": 1,
    "IL7R-related_disorder|not_specified|not_provided|Immunodeficiency_104": 2,
    "Immunodeficiency_104|Multiple_myeloma": 1,
    "not_specified|Immunodeficiency_104|not_provided": 4,
    "IL7R-related_disorder|Immunodeficiency_104|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency_disease|Immunodeficiency_104": 4,
    "Immunodeficiency_104|IL7R-related_disorder|not_provided": 1,
    "Immunodeficiency_104|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|Immunodeficiency_104|not_provided|Multiple_sclerosis|_susceptibility_to|_3": 1,
    "IL7R-related_disorder|Immunodeficiency_104": 1,
    "Immunodeficiency_104|not_specified|not_provided": 4,
    "IL7R-related_disorder|not_provided|Immunodeficiency_104|not_specified": 1,
    "Immunodeficiency_104|IL7R-related_disorder": 2,
    "T-B+_severe_combined_immunodeficiency_due_to_IL-7Ralpha_deficiency|not_provided|Immunodeficiency_104": 1,
    "Immunodeficiency_104|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "not_specified|Immunodeficiency_104|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "IL7R-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Immunodeficiency_104|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Immunodeficiency_104|not_specified": 2,
    "Developmental_delay_with_variable_neurologic_and_brain_abnormalities": 13,
    "Inborn_genetic_diseases|LMBRD2-related_disorder": 1,
    "LMBRD2-related_disorder": 5,
    "LMBRD2-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_delay_with_variable_neurologic_and_brain_abnormalities|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Developmental_delay_with_variable_neurologic_and_brain_abnormalities": 1,
    "See_cases|Inborn_genetic_diseases|Neurodevelopmental_disorder|LMBRD2-related_disorder|Developmental_delay_with_variable_neurologic_and_brain_abnormalities|not_provided": 1,
    "Developmental_delay|Dysmorphic_features|Motor_delay|brain_structure_abnormalities|Developmental_delay_with_variable_neurologic_and_brain_abnormalities": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements": 14,
    "LMBRD2-related_disorder|Developmental_delay_with_variable_neurologic_and_brain_abnormalities": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 154,
    "Inborn_genetic_diseases|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 13,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|NADK2-related_disorder|Inborn_genetic_diseases": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|Inborn_genetic_diseases": 8,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_provided|not_specified|NADK2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 1,
    "Bardet-Biedl_syndrome_10|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_specified": 4,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_provided": 2,
    "NADK2-related_disorder": 3,
    "not_provided|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 2,
    "not_specified|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 4,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|NADK2-related_disorder": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_specified|not_provided": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_provided|not_specified": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|NADK2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency": 1,
    "not_provided|Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_specified": 2,
    "Hereditary_episodic_ataxia": 7,
    "Episodic_ataxia_type_6": 53,
    "not_specified|not_provided|SLC1A3-related_disorder|Episodic_ataxia_type_6": 1,
    "not_provided|Episodic_ataxia_type_6": 6,
    "Episodic_ataxia_type_6|not_specified|not_provided": 3,
    "not_specified|not_provided|Episodic_ataxia_type_6": 3,
    "Episodic_ataxia_type_6|not_provided": 21,
    "SLC1A3-related_disorder": 1,
    "not_specified|Episodic_ataxia_type_6|not_provided": 2,
    "not_provided|Episodic_ataxia_type_6|not_specified": 2,
    "Inborn_genetic_diseases|Episodic_ataxia_type_6|not_provided": 1,
    "not_provided|Episodic_ataxia_type_6|Inborn_genetic_diseases": 2,
    "Episodic_ataxia_type_6|SLC1A3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_6": 2,
    "Episodic_ataxia_type_6|SLC1A3-related_disorder|not_provided": 1,
    "not_specified|Episodic_ataxia_type_6": 1,
    "SLC1A3-related_disorder|Episodic_ataxia_type_6": 1,
    "Episodic_ataxia_type_6|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Episodic_ataxia_type_6|Spastic_ataxia|not_provided": 1,
    "not_provided|Multiple_congenital_anomalies/dysmorphic_syndrome": 4,
    "not_provided|SLC1A3-related_disorder": 1,
    "SLC1A3-related_disorder|not_specified|not_provided|Episodic_ataxia_type_6": 1,
    "Hereditary_episodic_ataxia|not_provided": 1,
    "Cornelia_de_Lange_syndrome_1": 1194,
    "De_Lange_syndrome": 28,
    "not_provided|De_Lange_syndrome": 4,
    "not_provided|Cornelia_de_Lange_syndrome_1": 54,
    "Cornelia_de_Lange_syndrome_1|not_provided": 43,
    "not_specified|Cornelia_de_Lange_syndrome_1": 19,
    "Cornelia_de_Lange_syndrome_1|not_specified": 10,
    "NIPBL-related_disorder": 56,
    "NIPBL-related_disorder|Cornelia_de_Lange_syndrome_1": 9,
    "not_specified|not_provided|Cornelia_de_Lange_syndrome_1": 4,
    "not_provided|Cornelia_de_Lange_syndrome_1|NIPBL-related_disorder": 2,
    "Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|not_provided": 4,
    "Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases": 47,
    "Inborn_genetic_diseases|not_specified|Cornelia_de_Lange_syndrome_1|not_provided": 3,
    "NIPBL-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_1|NIPBL-related_disorder": 13,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1": 30,
    "Cornelia_de_Lange_syndrome_1|NIPBL-related_disorder|Inborn_genetic_diseases": 4,
    "NIPBL-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Cornelia_de_Lange_syndrome_1": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Cornelia_de_Lange_syndrome_1": 9,
    "NIPBL-related_disorder|not_provided|Cornelia_de_Lange_syndrome_1": 2,
    "Inborn_genetic_diseases|not_provided|Cornelia_de_Lange_syndrome_1": 9,
    "Cornelia_de_Lange_syndrome_1|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1": 4,
    "Vesicoureteral_reflux|Horseshoe_kidney|Intellectual_disability|_mild|Seizure|Plagiocephaly": 1,
    "Cornelia_de_Lange_syndrome_1|not_specified|not_provided": 4,
    "not_provided|Cornelia_de_Lange_syndrome_1|NIPBL-related_disorder|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|De_Lange_syndrome": 1,
    "not_specified|not_provided|De_Lange_syndrome|Cornelia_de_Lange_syndrome_1": 1,
    "NIPBL-related_disorder|Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|NIPBL-related_disorder|Cornelia_de_Lange_syndrome_1": 1,
    "not_provided|NIPBL-related_disorder": 1,
    "NIPBL-related_disorder|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1": 3,
    "Cornelia_de_Lange_syndrome_1|Fetal_growth_restriction|Cryptorchidism|Microretrognathia|Long_philtrum|Congenital_diaphragmatic_hernia|Single_umbilical_artery|Pulmonary_hypoplasia|Penile_hypospadias|Right_ventricular_hypertrophy": 1,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1|not_specified": 4,
    "not_specified|Inborn_genetic_diseases|NIPBL-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Cornelia_de_Lange_syndrome_1": 3,
    "not_provided|Cornelia_de_Lange_syndrome_1|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|Cornelia_de_Lange_syndrome_1": 1,
    "Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|NIPBL-related_disorder": 1,
    "NIPBL-related_disorder|Inborn_genetic_diseases|not_provided|Cornelia_de_Lange_syndrome_1": 4,
    "Cornelia_de_Lange_syndrome_1|NIPBL-related_disorder|not_specified": 1,
    "NIPBL-related_disorder|Cornelia_de_Lange_syndrome_1|not_provided": 2,
    "NIPBL-related_disorder|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1": 1,
    "NIPBL-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1|not_specified|not_provided": 2,
    "not_provided|Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Neurodevelopmental_delay|Cornelia_de_Lange_syndrome_1": 1,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_1|not_provided": 3,
    "Cornelia_de_Lange_syndrome_1|not_specified|Inborn_genetic_diseases": 2,
    "Cornelia_de_Lange_syndrome_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases": 1,
    "not_specified|Cornelia_de_Lange_syndrome_1|not_provided": 4,
    "not_provided|not_specified|Cornelia_de_Lange_syndrome_1": 1,
    "Cornelia_de_Lange_syndrome_1|not_provided|not_specified": 1,
    "not_specified|Cornelia_de_Lange_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "De_Lange_syndrome|Cornelia_de_Lange_syndrome_1": 1,
    "Cornelia_de_Lange_syndrome_1|not_provided|Inborn_genetic_diseases": 2,
    "Cornelia_de_Lange_syndrome_1|De_Lange_syndrome": 1,
    "not_specified|Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Cornelia_de_Lange_syndrome_1|not_specified|NIPBL-related_disorder": 1,
    "Inborn_genetic_diseases|NIPBL-related_disorder|not_specified|not_provided|Cornelia_de_Lange_syndrome_1": 1,
    "Global_developmental_delay|Abnormal_facial_shape|Intellectual_disability|Brachydactyly": 1,
    "Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|NIPBL-related_disorder|not_provided": 1,
    "not_specified|Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|NIPBL-related_disorder|Cornelia_de_Lange_syndrome_1": 1,
    "Cornelia_de_Lange_syndrome_1|not_provided|NIPBL-related_disorder": 2,
    "Cornelia_de_Lange_syndrome_1|Inborn_genetic_diseases|Global_developmental_delay": 1,
    "Cornelia_de_Lange_syndrome_1|Orofacial_cleft_1": 1,
    "See_cases|Cornelia_de_Lange_syndrome_1": 1,
    "Inborn_genetic_diseases|NIPBL-related_disorder": 1,
    "Cornelia_de_Lange_syndrome_1|Abnormal_brain_morphology": 1,
    "Tetralogy_of_Fallot|Cleft_palate|Microcephaly": 1,
    "Cornelia_de_Lange_syndrome_1|Intellectual_disability": 1,
    "Cornelia_de_Lange_syndrome_1|Intellectual_disability|Inborn_genetic_diseases|not_specified": 1,
    "Cornelia_de_Lange_syndrome_1|Developmental_and_epileptic_encephalopathy|_54": 1,
    "Cornelia_de_Lange_syndrome_1|not_provided|History_of_neurodevelopmental_disorder": 1,
    "not_specified|De_Lange_syndrome": 1,
    "De_Lange_syndrome|not_provided": 3,
    "Joubert_syndrome_17": 94,
    "not_provided|Joubert_syndrome_17": 40,
    "not_specified|Joubert_syndrome_17": 1,
    "CPLANE1-related_disorder": 9,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|not_provided": 86,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 229,
    "not_provided|Inborn_genetic_diseases|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 2,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided": 68,
    "not_provided|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 56,
    "not_provided|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 67,
    "CPLANE1-related_disorder|Joubert_syndrome_17|not_specified|not_provided": 1,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 6,
    "CPLANE1-related_disorder|not_provided|not_specified|Joubert_syndrome_17": 1,
    "not_specified|Joubert_syndrome_17|not_provided": 10,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_17|CPLANE1-related_disorder|Orofaciodigital_syndrome_type_6": 1,
    "not_provided|Joubert_syndrome_17|Joubert_syndrome|Joubert_syndrome_and_related_disorders|See_cases|Orofaciodigital_syndrome_type_6": 1,
    "not_specified|not_provided|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 4,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided": 3,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|CPLANE1-related_disorder|not_provided": 2,
    "not_provided|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|CPLANE1-related_disorder": 2,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|not_provided|Joubert_syndrome_1": 1,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|Inborn_genetic_diseases|not_provided": 3,
    "Joubert-orofaciodigital_syndrome": 1,
    "CPLANE1-related_disorder|not_specified|not_provided|Joubert_syndrome_17|Intellectual_disability": 1,
    "Joubert_syndrome_17|not_provided": 16,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|not_provided|Inborn_genetic_diseases": 2,
    "Joubert_syndrome|not_provided|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "CPLANE1-related_disorder|not_specified|not_provided|Joubert_syndrome_17": 2,
    "not_provided|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_specified": 1,
    "not_provided|Joubert_syndrome_17|CPLANE1-related_disorder": 2,
    "not_provided|CPLANE1-related_disorder|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "Joubert_syndrome|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Orofaciodigital_syndrome_type_6": 1,
    "not_provided|not_specified|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome_17|not_provided|Orofaciodigital_syndrome_type_6": 4,
    "CPLANE1-related_disorder|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|Inborn_genetic_diseases|not_specified|not_provided|See_cases": 1,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|CPLANE1-related_disorder|not_provided": 2,
    "Joubert_syndrome_17|not_provided|Global_developmental_delay|Jaundice|See_cases": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_and_related_disorders|not_provided": 1,
    "not_provided|Joubert_syndrome_17|not_specified|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_specified|not_provided": 3,
    "not_specified|not_provided|Inborn_genetic_diseases|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 1,
    "not_specified|not_provided|Joubert_syndrome_17": 12,
    "Median_cleft_lip_and_palate|Dysgenesis_of_the_cerebellar_vermis|Polydactyly|Encephalocele": 2,
    "Orofaciodigital_syndrome_type_6|not_provided|Joubert_syndrome_17|Global_developmental_delay|Typical_Joubert_syndrome_MRI_findings": 1,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|not_specified|not_provided": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided|Global_developmental_delay|Jaundice": 1,
    "CPLANE1-related_disorder|not_provided": 5,
    "Orofaciodigital_syndrome_type_6|not_provided|Joubert_syndrome_and_related_disorders": 1,
    "not_provided|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|Inborn_genetic_diseases": 2,
    "not_specified|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "not_provided|CPLANE1-related_disorder": 10,
    "Inborn_genetic_diseases|CPLANE1-related_disorder|not_provided": 1,
    "Joubert_syndrome_17|Joubert_syndrome_and_related_disorders|not_provided|Orofaciodigital_syndrome_type_6": 1,
    "not_provided|CPLANE1-related_disorder|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 2,
    "CPLANE1-related_disorder|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_specified|not_provided": 1,
    "Joubert_syndrome_17|CPLANE1-related_disorder": 1,
    "not_provided|Joubert_syndrome_17|not_specified": 4,
    "Inborn_genetic_diseases|Joubert_syndrome_17|not_provided|Orofaciodigital_syndrome_type_6": 1,
    "CPLANE1-related_disorder|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided": 5,
    "CPLANE1-related_disorder|not_provided|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "CPLANE1-related_disorder|not_specified|Joubert_syndrome_17|not_provided": 1,
    "Orofaciodigital_syndrome_type_6": 4,
    "not_provided|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Joubert_syndrome_17": 9,
    "Joubert_syndrome_17|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Orofaciodigital_syndrome_type_6|not_provided": 3,
    "not_provided|Joubert_syndrome_17|Inborn_genetic_diseases|CPLANE1-related_disorder|not_specified|Orofaciodigital_syndrome_type_6": 1,
    "Orofaciodigital_syndrome_type_6|not_provided|Joubert_syndrome_17": 2,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome_17|not_provided|Inborn_genetic_diseases|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome_17|not_specified|not_provided": 1,
    "CPLANE1-related_disorder|not_provided|Joubert_syndrome_17": 2,
    "Joubert_syndrome_17|not_provided|CPLANE1-related_disorder": 3,
    "Joubert_syndrome_17|not_specified": 1,
    "CPLANE1-related_disorder|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|not_provided": 2,
    "not_specified|not_provided|Joubert_syndrome_17|Intellectual_disability": 1,
    "not_specified|Joubert_syndrome_17|CPLANE1-related_disorder|not_provided": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided|Inborn_genetic_diseases": 3,
    "Joubert_syndrome|not_provided|not_specified": 2,
    "not_specified|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided": 1,
    "not_provided|Craniosynostosis_syndrome": 2,
    "Joubert_syndrome_17|Joubert_syndrome_and_related_disorders|Joubert_syndrome_1|Orofaciodigital_syndrome_type_6|not_provided": 1,
    "not_provided|Orofaciodigital_syndrome_type_6": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Joubert_syndrome_17": 1,
    "not_specified|not_provided|CPLANE1-related_disorder": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_17|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_17|CPLANE1-related_disorder|Orofaciodigital_syndrome_type_6": 1,
    "not_provided|Joubert_syndrome": 21,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_17": 1,
    "not_provided|Joubert_syndrome_and_related_disorders|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|See_cases|Joubert_syndrome_1|not_provided": 2,
    "not_specified|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|not_provided": 2,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|CPLANE1-related_disorder": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_specified": 1,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|Joubert_syndrome_and_related_disorders": 1,
    "CPLANE1-related_disorder|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided|Inborn_genetic_diseases|Joubert_syndrome_and_related_disorders": 1,
    "CPLANE1-related_disorder|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|Nephronophthisis|Inborn_genetic_diseases|not_provided|Global_developmental_delay|Jaundice": 1,
    "Joubert_syndrome_17|not_provided|Orofaciodigital_syndrome_type_6|not_specified": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided": 1,
    "Joubert_syndrome_17|not_provided|not_specified": 1,
    "not_provided|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|CPLANE1-related_disorder": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_17|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Orofaciodigital_syndrome_type_6|Joubert_syndrome_17": 1,
    "Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided|Joubert_syndrome_1": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_17|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_17": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_17": 1,
    "Orofaciodigital_syndrome_type_6|Joubert_syndrome_17|Nephronophthisis|not_provided|Joubert_syndrome_and_related_disorders|not_specified|CPLANE1-related_disorder": 1,
    "Cleft_palate|Astrocytoma|Cleft_lip|not_provided": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|Joubert_syndrome_and_related_disorders": 1,
    "CPLANE1-related_disorder|Joubert_syndrome_17|Orofaciodigital_syndrome_type_6|not_provided|Inborn_genetic_diseases": 1,
    "NUP155-related_disorder": 8,
    "NUP155-related_disorder|not_provided": 4,
    "Atrial_fibrillation|_familial|_15": 5,
    "not_provided|NUP155-related_disorder": 3,
    "Atrial_fibrillation|_familial|_15|not_specified": 1,
    "not_provided|Atrial_fibrillation|_familial|_15": 1,
    "Hirschsprung_disease|_susceptibility_to|_3": 64,
    "Hirschsprung_Disease|_Dominant|not_provided": 2,
    "Hirschsprung_disease|_susceptibility_to|_3|not_provided": 6,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_3": 8,
    "Hirschsprung_Disease|_Dominant": 4,
    "not_provided|Hirschsprung_Disease|_Dominant": 1,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_3": 1,
    "Hirschsprung_disease|_susceptibility_to|_3|not_specified": 3,
    "not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_3": 1,
    "GDNF-related_disorder": 3,
    "GDNF-related_disorder|not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_3": 2,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_3|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_3|not_provided|not_specified|GDNF-related_disorder": 1,
    "GDNF-related_disorder|not_provided": 1,
    "Stuve-Wiedemann_syndrome": 227,
    "not_provided|Stuve-Wiedemann_syndrome": 44,
    "Stuve-Wiedemann_syndrome|not_provided": 47,
    "not_provided|St\u00fcve-Wiedemann_syndrome_1": 16,
    "Stuve-Wiedemann_syndrome|not_specified|LIFR-related_disorder|St\u00fcve-Wiedemann_syndrome_1|not_provided": 1,
    "St\u00fcve-Wiedemann_syndrome_1|not_provided|Stuve-Wiedemann_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_specified|LIFR-related_disorder": 1,
    "St\u00fcve-Wiedemann_syndrome_1|not_provided": 24,
    "Inborn_genetic_diseases|Stuve-Wiedemann_syndrome": 5,
    "Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "St\u00fcve-Wiedemann_syndrome_1": 86,
    "Inborn_genetic_diseases|St\u00fcve-Wiedemann_syndrome_1|not_provided": 3,
    "Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1": 4,
    "St\u00fcve-Wiedemann_syndrome_1|Inborn_genetic_diseases": 3,
    "LIFR-related_disorder|not_provided": 4,
    "St\u00fcve-Wiedemann_syndrome_1|Stuve-Wiedemann_syndrome|not_provided": 1,
    "not_provided|LIFR-related_disorder": 5,
    "Connective_tissue_disorder|Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1|not_specified|not_provided": 2,
    "Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1|not_provided": 4,
    "LIFR-related_disorder": 1,
    "Inborn_genetic_diseases|St\u00fcve-Wiedemann_syndrome_1": 7,
    "Inborn_genetic_diseases|Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|St\u00fcve-Wiedemann_syndrome_1": 2,
    "Stuve-Wiedemann_syndrome|not_provided|Connective_tissue_disorder": 1,
    "not_provided|LIFR-related_disorder|St\u00fcve-Wiedemann_syndrome_1|Stuve-Wiedemann_syndrome": 1,
    "Stuve-Wiedemann_syndrome|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|Stuve-Wiedemann_syndrome|LIFR-related_disorder|not_provided": 1,
    "LIFR-related_disorder|not_provided|St\u00fcve-Wiedemann_syndrome_1|Stuve-Wiedemann_syndrome|Connective_tissue_disorder": 1,
    "St\u00fcve-Wiedemann_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "St\u00fcve-Wiedemann_syndrome_1|Connective_tissue_disorder|not_provided|Stuve-Wiedemann_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|St\u00fcve-Wiedemann_syndrome_1": 2,
    "Stuve-Wiedemann_syndrome|not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "St\u00fcve-Wiedemann_syndrome_1|Stuve-Wiedemann_syndrome": 2,
    "not_provided|St\u00fcve-Wiedemann_syndrome_1|Connective_tissue_disorder": 2,
    "Congenital_anomaly_of_kidney_and_urinary_tract|LIFR-related_disorder|St\u00fcve-Wiedemann_syndrome_1|Connective_tissue_disorder|not_provided|Stuve-Wiedemann_syndrome|not_specified": 1,
    "not_provided|Stuve-Wiedemann_syndrome|LIFR-related_disorder": 1,
    "not_specified|Stuve-Wiedemann_syndrome|Connective_tissue_disorder|not_provided|St\u00fcve-Wiedemann_syndrome_1": 1,
    "Hypotonia|Developmental_regression|Abnormal_cerebral_white_matter_morphology|Epileptic_encephalopathy|Global_developmental_delay|Absent_speech": 1,
    "Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1|Inborn_genetic_diseases": 1,
    "St\u00fcve-Wiedemann_syndrome_1|not_provided|Stuve-Wiedemann_syndrome": 1,
    "Stuve-Wiedemann_syndrome|not_provided|St\u00fcve-Wiedemann_syndrome_1": 4,
    "St\u00fcve-Wiedemann_syndrome_1|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Stuve-Wiedemann_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Stuve-Wiedemann_syndrome": 1,
    "LIFR-related_disorder|Stuve-Wiedemann_syndrome|not_provided": 1,
    "not_provided|Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1": 4,
    "LIFR-related_disorder|not_provided|Stuve-Wiedemann_syndrome": 1,
    "not_provided|St\u00fcve-Wiedemann_syndrome_1|Stuve-Wiedemann_syndrome": 1,
    "Connective_tissue_disorder|Stuve-Wiedemann_syndrome|not_provided": 1,
    "St\u00fcve-Wiedemann_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "St\u00fcve-Wiedemann_syndrome_1|Inborn_genetic_diseases|Stuve-Wiedemann_syndrome": 1,
    "Inborn_genetic_diseases|Stuve-Wiedemann_syndrome|St\u00fcve-Wiedemann_syndrome_1|Connective_tissue_disorder|not_provided": 1,
    "not_provided|LIFR-related_disorder|Stuve-Wiedemann_syndrome": 1,
    "not_specified|Stuve-Wiedemann_syndrome|Connective_tissue_disorder|not_provided": 1,
    "St\u00fcve-Wiedemann_syndrome_1|LIFR-related_disorder|Stuve-Wiedemann_syndrome|Connective_tissue_disorder|not_provided": 1,
    "Stuve-Wiedemann_syndrome|not_provided|not_specified": 1,
    "Stuve-Wiedemann_syndrome|not_provided|St\u00fcve-Wiedemann_syndrome_1|not_specified": 1,
    "not_provided|St\u00fcve-Wiedemann_syndrome_1|Inborn_genetic_diseases": 1,
    "OSMR-related_disorder|not_provided": 2,
    "OSMR-related_disorder": 9,
    "Inborn_genetic_diseases|OSMR-related_disorder": 1,
    "Amyloidosis|_primary_localized_cutaneous|_1": 8,
    "not_provided|OSMR-related_disorder": 2,
    "Inborn_genetic_diseases|Amyloidosis|_primary_localized_cutaneous|_1": 1,
    "not_provided|Amyloidosis|_primary_localized_cutaneous|_1": 1,
    "OSMR-related_disorder|Inborn_genetic_diseases": 1,
    "Thrombocytopenia_3": 4,
    "FYB1-related_disorder": 13,
    "FYB1-related_disorder|not_specified": 2,
    "not_provided|FYB1-related_disorder": 1,
    "FYB1-related_disorder|not_provided": 2,
    "Complement_component_9_deficiency|not_provided|Age_related_macular_degeneration_15": 1,
    "not_provided|C9-related_disorder": 9,
    "Complement_component_9_deficiency|Age_related_macular_degeneration_15|not_provided": 1,
    "Complement_component_9_deficiency": 3,
    "not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_15|Complement_component_9_deficiency": 1,
    "C9-related_disorder|not_provided": 3,
    "Complement_component_9_deficiency|Age_related_macular_degeneration_15": 1,
    "not_provided|Complement_component_9_deficiency": 4,
    "Complement_component_9_deficiency|Age_related_macular_degeneration_15|C9-related_disorder|not_provided": 1,
    "not_provided|Age_related_macular_degeneration_15|Complement_component_9_deficiency": 2,
    "not_provided|Complement_component_9_deficiency|Age_related_macular_degeneration_15": 2,
    "Complement_component_9_deficiency|not_provided": 2,
    "Age_related_macular_degeneration_15|not_provided": 1,
    "Age_related_macular_degeneration_15|Complement_component_9_deficiency|not_provided": 2,
    "C9-related_disorder": 2,
    "Age_related_macular_degeneration_15": 1,
    "C9-related_disorder|Complement_component_9_deficiency|Age_related_macular_degeneration_15|not_provided": 1,
    "not_provided|Complement_component_9_deficiency|C9-related_disorder": 1,
    "Teratocarcinoma": 1,
    "Primary_amenorrhea": 3,
    "not_provided|Complement_component_7_deficiency": 10,
    "Complement_component_7_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "C7-related_disorder|not_provided": 7,
    "not_provided|C7-related_disorder": 3,
    "Complement_component_7_deficiency|not_provided": 8,
    "Complement_component_7_deficiency": 5,
    "not_provided|C7-related_disorder|Complement_component_7_deficiency": 1,
    "Complement_component_7_deficiency|C7-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Complement_component_7_deficiency": 1,
    "not_provided|Complement_component_7_deficiency|Inborn_genetic_diseases": 1,
    "C7-related_disorder|not_provided|not_specified|Complement_component_7_deficiency|C7_and_C6_deficiency|_combined_subtotal": 1,
    "C7-related_disorder": 1,
    "Complement_component_7_deficiency|not_specified": 1,
    "Complement_component_6_deficiency": 9,
    "not_provided|C6-related_disorder": 6,
    "not_provided|Complement_component_6_deficiency": 7,
    "not_specified|C6_deficiency|_subtotal|Complement_component_6_deficiency|C6-related_disorder|not_provided": 1,
    "Complement_component_6_deficiency|not_provided": 6,
    "C6-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Complement_component_6_deficiency": 2,
    "C6-related_disorder|not_provided|Complement_component_6_deficiency": 1,
    "not_specified|C6-related_disorder|not_provided": 1,
    "Complement_component_6_deficiency|C6-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Complement_component_6_deficiency|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Complement_component_6_deficiency": 1,
    "not_specified|Complement_component_6_deficiency|not_provided": 1,
    "C6-related_disorder": 5,
    "Immunodeficiency_due_to_a_late_component_of_complement_deficiency|Complement_component_6_deficiency|not_provided|C6-related_disorder": 1,
    "not_provided|Complement_component_6_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Complement_component_6_deficiency|C6-related_disorder": 1,
    "C6-related_disorder|Complement_component_6_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|C6-related_disorder": 1,
    "Complement_component_6_deficiency|not_provided|C6-related_disorder": 2,
    "C6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "C6_A/B_POLYMORPHISM": 1,
    "not_provided|not_specified|C6-related_disorder": 1,
    "Succinyl-CoA_acetoacetate_transferase_deficiency": 157,
    "OXCT1-related_disorder": 3,
    "not_provided|Succinyl-CoA_acetoacetate_transferase_deficiency": 7,
    "Succinyl-CoA_acetoacetate_transferase_deficiency|not_provided": 5,
    "Succinyl-CoA_acetoacetate_transferase_deficiency|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Succinyl-CoA_acetoacetate_transferase_deficiency": 4,
    "not_provided|not_specified|Succinyl-CoA_acetoacetate_transferase_deficiency": 1,
    "OXCT1-related_disorder|Succinyl-CoA_acetoacetate_transferase_deficiency": 5,
    "Succinyl-CoA_acetoacetate_transferase_deficiency|OXCT1-related_disorder": 3,
    "not_provided|Succinyl-CoA_acetoacetate_transferase_deficiency|OXCT1-related_disorder": 2,
    "Succinyl-CoA_acetoacetate_transferase_deficiency|OXCT1-related_disorder|not_provided": 2,
    "not_provided|Succinyl-CoA_acetoacetate_transferase_deficiency|not_specified": 2,
    "not_specified|Succinyl-CoA_acetoacetate_transferase_deficiency": 1,
    "OXCT1-related_disorder|not_specified|not_provided|Succinyl-CoA_acetoacetate_transferase_deficiency": 1,
    "Laron-type_isolated_somatotropin_defect": 75,
    "Laron-type_isolated_somatotropin_defect|not_provided": 10,
    "GHR-related_disorder": 2,
    "Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect": 1,
    "not_provided|Laron-type_isolated_somatotropin_defect|Inborn_genetic_diseases": 1,
    "not_provided|Laron-type_isolated_somatotropin_defect|not_specified": 2,
    "Laron-type_isolated_somatotropin_defect|Growth_hormone_insensitivity_syndrome": 1,
    "not_provided|Growth_hormone_insensitivity_syndrome|Laron-type_isolated_somatotropin_defect": 1,
    "Laron-type_isolated_somatotropin_defect|Short_stature_due_to_partial_GHR_deficiency|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "not_provided|Laron-type_isolated_somatotropin_defect|Short_stature_due_to_partial_GHR_deficiency": 1,
    "Growth_hormone_insensitivity_syndrome|Short_stature_due_to_partial_GHR_deficiency|not_provided": 1,
    "Laron-type_isolated_somatotropin_defect|Growth_hormone_insensitivity_syndrome|not_provided": 1,
    "Growth_hormone_insensitivity_syndrome": 1,
    "not_specified|not_provided|Laron-type_isolated_somatotropin_defect": 3,
    "not_provided|Laron-type_isolated_somatotropin_defect": 15,
    "Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect|Hypercholesterolemia|_familial|_1": 1,
    "Laron_syndrome_with_undetectable_serum_GH-binding_protein|Growth_hormone_insensitivity_syndrome": 1,
    "Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect|not_provided": 1,
    "not_specified|not_provided|Short_stature_due_to_partial_GHR_deficiency|Hypercholesterolemia|_familial|_1|Laron-type_isolated_somatotropin_defect": 1,
    "not_specified|Short_stature_due_to_partial_GHR_deficiency": 1,
    "not_provided|not_specified|Laron-type_isolated_somatotropin_defect": 1,
    "Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect|GHR-related_disorder|Hypercholesterolemia|_familial|_1|Short_stature_due_to_growth_hormone_secretagogue_receptor_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hypercholesterolemia|_familial|_1|Laron-type_isolated_somatotropin_defect|Short_stature_due_to_partial_GHR_deficiency": 1,
    "Short_stature_due_to_partial_GHR_deficiency|not_provided|not_specified|Laron-type_isolated_somatotropin_defect": 1,
    "not_provided|Laron-type_isolated_somatotropin_defect|Hypercholesterolemia|_familial|_1|Short_stature_due_to_partial_GHR_deficiency": 2,
    "Laron-type_isolated_somatotropin_defect|Short_stature_due_to_partial_GHR_deficiency|Hypercholesterolemia|_familial|_1": 2,
    "Laron-type_isolated_somatotropin_defect|Hypercholesterolemia|_familial|_1|Short_stature_due_to_partial_GHR_deficiency": 2,
    "not_specified|not_provided|Laron-type_isolated_somatotropin_defect|Short_stature_due_to_partial_GHR_deficiency": 1,
    "Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect|not_provided|Genu_varum|Relative_macrocephaly|Mesomelic/rhizomelic_limb_shortening|Specific_learning_disability|Seizure|Short_stature|Disproportionate_short-limb_short_stature": 1,
    "Laron_syndrome_with_undetectable_serum_GH-binding_protein": 2,
    "Short_stature_due_to_partial_GHR_deficiency|not_provided": 2,
    "Hypercholesterolemia|_familial|_1|Laron-type_isolated_somatotropin_defect|not_provided": 1,
    "not_specified|Laron-type_isolated_somatotropin_defect|not_provided": 2,
    "Laron_syndrome_with_elevated_serum_GH-binding_protein": 2,
    "not_provided|not_specified|GHR-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Short_stature_due_to_partial_GHR_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect": 1,
    "Laron-type_isolated_somatotropin_defect|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Laron-type_isolated_somatotropin_defect|Hypercholesterolemia|_familial|_1|Short_stature_due_to_partial_GHR_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Short_stature_due_to_partial_GHR_deficiency": 1,
    "Laron-type_isolated_somatotropin_defect|not_provided|not_specified": 1,
    "not_provided|GHR-related_disorder|Laron-type_isolated_somatotropin_defect": 1,
    "GHR-related_disorder|not_provided": 1,
    "not_provided|GHR-related_disorder": 1,
    "Hypercholesterolemia|_familial|_1|Short_stature_due_to_partial_GHR_deficiency|Laron-type_isolated_somatotropin_defect": 1,
    "not_specified|not_provided|Short_stature_due_to_partial_GHR_deficiency|Inborn_genetic_diseases": 1,
    "Hypercholesterolemia|_familial|_1|Laron-type_isolated_somatotropin_defect|not_specified|not_provided|Short_stature_due_to_partial_GHR_deficiency": 1,
    "Rigid_spine_syndrome": 7,
    "not_provided|Glucocorticoid_deficiency_4": 3,
    "Glucocorticoid_deficiency_4|not_specified|not_provided": 1,
    "not_provided|NNT-related_disorder": 5,
    "Glucocorticoid_deficiency_4|not_provided": 2,
    "Glucocorticoid_deficiency_4": 21,
    "NNT-related_disorder|not_provided": 7,
    "GLUCOCORTICOID_DEFICIENCY_4_WITH_MINERALOCORTICOID_DEFICIENCY|Glucocorticoid_deficiency_4": 1,
    "NNT-related_disorder": 7,
    "GLUCOCORTICOID_DEFICIENCY_4_WITH_MINERALOCORTICOID_DEFICIENCY": 1,
    "Glucocorticoid_deficiency_4|Inborn_genetic_diseases|not_provided": 1,
    "NNT-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Glucocorticoid_deficiency_4|NNT-related_disorder": 1,
    "Inborn_genetic_diseases|Glucocorticoid_deficiency_4": 1,
    "NNT-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_absence_of_salivary_gland|Levy-Hollister_syndrome": 2,
    "Interstitial_lung_disease_specific_to_childhood": 1,
    "FGF10-related_disorder|Congenital_absence_of_salivary_gland|Levy-Hollister_syndrome|not_specified|not_provided": 1,
    "Lacrimoauriculodentodigital_syndrome_3|Congenital_absence_of_salivary_gland|not_provided": 1,
    "Congenital_absence_of_salivary_gland|Lacrimoauriculodentodigital_syndrome_3|not_provided": 2,
    "not_provided|Congenital_absence_of_salivary_gland": 3,
    "Levy-Hollister_syndrome": 12,
    "Levy-Hollister_syndrome|FGF10-related_disorder": 1,
    "Lacrimoauriculodentodigital_syndrome_3": 5,
    "Congenital_absence_of_salivary_gland|Lacrimoauriculodentodigital_syndrome_3": 8,
    "Congenital_absence_of_salivary_gland": 5,
    "Congenital_absence_of_salivary_gland|not_provided": 1,
    "Lacrimoauriculodentodigital_syndrome_3|Congenital_absence_of_salivary_gland": 1,
    "Congenital_absence_of_salivary_gland|Levy-Hollister_syndrome": 1,
    "Congenital_absence_of_salivary_gland|Inborn_genetic_diseases|Levy-Hollister_syndrome": 1,
    "Levy-Hollister_syndrome|not_provided": 1,
    "not_provided|Congenital_absence_of_salivary_gland|FGF10-related_disorder": 1,
    "FGF10-related_disorder": 4,
    "Congenital_absence_of_salivary_gland|not_specified|FGF10-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_absence_of_salivary_gland|Lacrimoauriculodentodigital_syndrome_3|not_provided": 1,
    "HCN1-related_disorder|Developmental_and_epileptic_encephalopathy": 4,
    "Developmental_and_epileptic_encephalopathy|_24": 17,
    "HCN1-related_disorder": 5,
    "Developmental_and_epileptic_encephalopathy|HCN1-related_disorder": 5,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_24": 1,
    "HCN1-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|HCN1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10": 16,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|_24": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|_24": 3,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_24": 3,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|not_provided|HCN1-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_10": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Generalized_epilepsy_with_febrile_seizures_plus|_type_10": 2,
    "Inborn_genetic_diseases|HCN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_10": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_10": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_24": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_24|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Epileptic_encephalopathy": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|_24|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_10": 1,
    "Developmental_and_epileptic_encephalopathy|_24|not_provided": 2,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy": 4,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|not_provided": 1,
    "Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Seizure|Color_vision_defect": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|_24|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_24|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_24": 2,
    "HCN1-related_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|HCN1-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|HCN1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|_24|Inborn_genetic_diseases|not_provided": 1,
    "HCN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "HCN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_24|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 3,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Developmental_and_epileptic_encephalopathy|_24|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_24|Generalized_epilepsy_with_febrile_seizures_plus|_type_10|Inborn_genetic_diseases|HCN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|HCN1-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 13,
    "ISL1-related_disorder": 72,
    "not_specified|ISL1-related_disorder": 7,
    "not_provided|ISL1-related_disorder": 1,
    "Platelet-type_bleeding_disorder_9|not_provided": 11,
    "Platelet-type_bleeding_disorder_9": 121,
    "not_provided|Platelet-type_bleeding_disorder_9": 25,
    "Platelet-type_bleeding_disorder_9|Inborn_genetic_diseases": 5,
    "Platelet-type_bleeding_disorder_9|ITGA2-related_disorder": 2,
    "not_provided|Platelet-type_bleeding_disorder_9|ITGA2-related_disorder": 4,
    "Inborn_genetic_diseases|Platelet-type_bleeding_disorder_9": 4,
    "ITGA2-related_disorder": 9,
    "Inborn_genetic_diseases|Platelet-type_bleeding_disorder_9|ITGA2-related_disorder": 2,
    "ITGA2-related_disorder|Platelet-type_bleeding_disorder_9": 2,
    "Platelet-type_bleeding_disorder_9|Fetal_and_neonatal_alloimmune_thrombocytopenia|not_provided": 1,
    "not_provided|ITGA2-related_disorder|Platelet-type_bleeding_disorder_9": 1,
    "not_provided|not_specified|Platelet-type_bleeding_disorder_9": 1,
    "Combined_molybdoflavoprotein_enzyme_deficiency|Platelet-type_bleeding_disorder_9": 7,
    "not_provided|Platelet-type_bleeding_disorder_9|Combined_molybdoflavoprotein_enzyme_deficiency": 3,
    "Combined_molybdoflavoprotein_enzyme_deficiency|not_provided|Platelet-type_bleeding_disorder_9": 7,
    "not_provided|Combined_molybdoflavoprotein_enzyme_deficiency|Platelet-type_bleeding_disorder_9": 3,
    "Platelet-type_bleeding_disorder_9|Combined_molybdoflavoprotein_enzyme_deficiency|not_provided": 1,
    "Platelet-type_bleeding_disorder_9|Combined_molybdoflavoprotein_enzyme_deficiency": 2,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|Platelet-type_bleeding_disorder_9": 3,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 30,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 52,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|Platelet-type_bleeding_disorder_9|not_provided": 4,
    "Platelet-type_bleeding_disorder_9|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|not_provided": 10,
    "Platelet-type_bleeding_disorder_9|Combined_molybdoflavoprotein_enzyme_deficiency|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 2,
    "Combined_molybdoflavoprotein_enzyme_deficiency|Platelet-type_bleeding_disorder_9|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "not_provided|MOCS2-related_disorder": 2,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|Abnormality_of_metabolism/homeostasis": 1,
    "MOCS2-related_disorder": 1,
    "not_provided|Combined_molybdoflavoprotein_enzyme_deficiency": 4,
    "not_specified|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "not_provided|Combined_molybdoflavoprotein_enzyme_deficiency|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|Inborn_genetic_diseases": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|MOCS2-related_disorder|not_provided": 2,
    "Combined_molybdoflavoprotein_enzyme_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 4,
    "not_provided|Inborn_genetic_diseases|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "Combined_molybdoflavoprotein_enzyme_deficiency|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|not_provided": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|not_specified|not_provided": 1,
    "Combined_molybdoflavoprotein_enzyme_deficiency|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Orofacial_cleft|not_provided": 1,
    "NDUFS4-related_disorder": 2,
    "Leigh_syndrome|not_specified|NDUFS4-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|Leigh_syndrome|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Inborn_genetic_diseases|NDUFS4-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|Leigh_syndrome|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Leigh_syndrome|NDUFS4-related_disorder|not_specified|not_provided": 1,
    "Mitochondrial_disease|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_provided": 1,
    "not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "not_provided|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 6,
    "Leigh_syndrome|not_provided|Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_specified|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "See_cases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|Inborn_genetic_diseases": 1,
    "ARL15-related_disorder": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_2C": 44,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2C": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_2C|not_specified": 3,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_type_2C": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2C|not_provided": 2,
    "not_provided|not_specified|Neuronopathy|_distal_hereditary_motor|_type_2C": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2C|not_specified|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_42|Primary_ciliary_dyskinesia": 2,
    "Ciliary_dyskinesia|_primary|_42": 6,
    "MCIDAS-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Ciliary_dyskinesia|_primary|_42|Primary_ciliary_dyskinesia|Inborn_genetic_diseases": 1,
    "MCIDAS-related_disorder|Primary_ciliary_dyskinesia|Ciliary_dyskinesia|_primary|_42|not_provided": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Ciliary_dyskinesia|_primary|_42": 1,
    "Inborn_genetic_diseases|Ciliary_dyskinesia|_primary|_42|Primary_ciliary_dyskinesia": 1,
    "not_specified|Ciliary_dyskinesia|_primary|_42|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|MCIDAS-related_disorder": 1,
    "MCIDAS-related_disorder|Inborn_genetic_diseases": 1,
    "Ciliary_dyskinesia|_primary|_42|Primary_ciliary_dyskinesia|MCIDAS-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Ciliary_dyskinesia|_primary|_42": 1,
    "Ciliary_dyskinesia|_primary|_42|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|CCNO-related_disorder": 4,
    "Primary_ciliary_dyskinesia_29|Primary_ciliary_dyskinesia": 6,
    "Primary_ciliary_dyskinesia|CCNO-related_disorder|not_provided": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_29|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia_29|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia_29|not_provided|Primary_ciliary_dyskinesia": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_29|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_29|not_provided": 1,
    "IL31RA-related_disorder": 8,
    "not_provided|Amyloidosis|_primary_localized_cutaneous|_2": 2,
    "not_provided|IL31RA-related_disorder|not_specified": 1,
    "IL31RA-related_disorder|not_provided": 1,
    "Amyloidosis|_primary_localized_cutaneous|_2": 2,
    "Amyloidosis|_primary_localized_cutaneous|_2|not_specified": 1,
    "not_provided|Amyloidosis|_primary_localized_cutaneous|_2|IL31RA-related_disorder": 1,
    "Amyloidosis|_primary_localized_cutaneous|_2|not_provided": 1,
    "not_specified|Amyloidosis|_primary_localized_cutaneous|_2": 1,
    "Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive|Stuve-Wiedemann_syndrome_2|Hyper-IgE_recurrent_infection_syndrome_4A|_autosomal_dominant|not_specified": 1,
    "IL6ST-related_disorder": 3,
    "IL6ST-related_disorder|not_provided": 4,
    "not_provided|IL6ST-related_disorder": 14,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_4A|_autosomal_dominant": 5,
    "Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive|Immunodeficiency_94_with_autoinflammation_and_dysmorphic_facies|Hyper-IgE_recurrent_infection_syndrome_4A|_autosomal_dominant|Stuve-Wiedemann_syndrome_2": 1,
    "Developmental_and_epileptic_encephalopathy|_7": 96,
    "Hyper-IgE_recurrent_infection_syndrome_4A|_autosomal_dominant|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|Hyper-IgE_recurrent_infection_syndrome_4A|_autosomal_dominant": 1,
    "not_provided|IL6ST-related_disorder|not_specified": 1,
    "not_specified|IL6ST-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_7|not_specified": 1,
    "IL6ST-related_disorder|not_specified": 1,
    "Stuve-Wiedemann_syndrome_2": 2,
    "not_provided|Stuve-Wiedemann_syndrome_2": 1,
    "Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive|GP130-deficient_hyper-IgE_syndrome|not_provided": 2,
    "Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive": 2,
    "not_specified|not_provided|IL6ST-related_disorder": 2,
    "Stuve-Wiedemann_syndrome_2|Stuve-Wiedemann_syndrome|not_provided": 1,
    "Immunodeficiency_94_with_autoinflammation_and_dysmorphic_facies": 3,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive": 1,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive|not_specified|IL6ST-related_disorder": 1,
    "Stuve-Wiedemann_syndrome_2|Immunodeficiency_94_with_autoinflammation_and_dysmorphic_facies|Hyper-IgE_recurrent_infection_syndrome_4A|_autosomal_dominant|Hyper-IgE_recurrent_infection_syndrome_4|_autosomal_recessive|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F": 20,
    "not_specified|46|XY_sex_reversal_6": 7,
    "46|XY_sex_reversal_6": 119,
    "46|XY_sex_reversal_6|Inborn_genetic_diseases": 10,
    "46|XY_sex_reversal_6|not_provided": 19,
    "not_provided|46|XY_sex_reversal_6": 8,
    "Inborn_genetic_diseases|46|XY_sex_reversal_6": 4,
    "MAP3K1-related_disorder": 7,
    "not_provided|46|XY_sex_reversal_6|not_specified": 2,
    "46|XY_sex_reversal_6|not_specified": 2,
    "46|XY_sex_reversal_6|not_specified|not_provided": 2,
    "46|XY_sex_reversal_6|Hearing_impairment": 1,
    "46|XY_sex_reversal_6|See_cases": 1,
    "MAP3K1-related_disorder|46|XY_sex_reversal_6": 5,
    "not_specified|not_provided|46|XY_sex_reversal_6": 1,
    "46|XY_sex_reversal_6|not_specified|MAP3K1-related_disorder": 1,
    "46|XY_sex_reversal_6|MAP3K1-related_disorder|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|46|XY_sex_reversal_6": 1,
    "MAP3K1-related_disorder|not_provided|46|XY_sex_reversal_6": 1,
    "46|XY_sex_reversal_6|Inborn_genetic_diseases|MAP3K1-related_disorder": 1,
    "Inborn_genetic_diseases|46|XY_sex_reversal_6|not_specified": 1,
    "MAP3K1-related_disorder|46|XY_sex_reversal_6|not_provided": 1,
    "not_provided|not_specified|46|XY_sex_reversal_6": 1,
    "46|XY_sex_reversal_6|MAP3K1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|46|XY_sex_reversal_6": 1,
    "Hearing_loss": 4,
    "Acrodysostosis_2_with_or_without_hormone_resistance": 107,
    "Acrodysostosis_2_with_or_without_hormone_resistance|not_provided": 40,
    "Acrodysostosis": 19,
    "not_provided|Acrodysostosis_2_with_or_without_hormone_resistance": 18,
    "Acrodysostosis|not_provided": 4,
    "not_provided|PDE4D-related_disorder": 5,
    "PDE4D-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Acrodysostosis_2_with_or_without_hormone_resistance|Inborn_genetic_diseases": 1,
    "PDE4D-related_disorder|not_provided": 3,
    "PDE4D-related_disorder": 15,
    "Acrodysostosis_2_with_or_without_hormone_resistance|PDE4D-related_disorder|not_provided": 1,
    "Postaxial_polydactyly-anterior_pituitary_anomalies-facial_dysmorphism_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Acrodysostosis": 1,
    "Acrodysostosis_2_with_or_without_hormone_resistance|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Acrodysostosis_2_with_or_without_hormone_resistance": 1,
    "Acrodysostosis_2_with_or_without_hormone_resistance|not_provided|PDE4D-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Acrodysostosis_2_with_or_without_hormone_resistance": 2,
    "Albright_hereditary_osteodystrophy|_pseudohypoparathyroidism|_pseudopseudohypoparathyroidism|_acrodysostosis_and_osteoma_cutis|Acrodysostosis_2_with_or_without_hormone_resistance": 1,
    "PDE4D-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PDE4D-related_disorder|Craniosynostosis_syndrome|Acrodysostosis_2_with_or_without_hormone_resistance": 1,
    "Cockayne_syndrome_type_1": 57,
    "Cockayne_syndrome_type_1|not_provided": 14,
    "not_provided|Cockayne_syndrome_type_1": 19,
    "Cockayne_syndrome": 6,
    "Cockayne_syndrome_type_1|UV-sensitive_syndrome_2|not_provided": 5,
    "Cockayne_syndrome_type_1|UV-sensitive_syndrome_2": 9,
    "UV-sensitive_syndrome_2|not_provided": 1,
    "Cockayne_syndrome_type_1|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Cockayne_syndrome_type_1": 1,
    "UV-sensitive_syndrome_2|Cockayne_syndrome_type_1|not_provided": 2,
    "not_provided|UV-sensitive_syndrome_2|Cockayne_syndrome_type_1": 5,
    "not_provided|Cockayne_syndrome|Cockayne_syndrome_type_1": 3,
    "Inborn_genetic_diseases|Cockayne_syndrome_type_1": 1,
    "ERCC8-related_disorder|not_provided": 2,
    "ERCC8-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Cockayne_syndrome_type_1": 1,
    "Cockayne_syndrome_type_1|Cockayne_syndrome|not_provided|UV-sensitive_syndrome_2": 1,
    "UV-sensitive_syndrome_2|Cockayne_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cockayne_syndrome_type_1|UV-sensitive_syndrome_2|Cockayne_syndrome": 1,
    "not_provided|Cockayne_syndrome_type_1|UV-sensitive_syndrome_2": 3,
    "Cockayne_syndrome|ERCC8-related_disorder|not_provided": 1,
    "ERCC8-related_disorder": 1,
    "UV-sensitive_syndrome_2|Cockayne_syndrome_type_1": 1,
    "Cockayne_syndrome|Cockayne_syndrome_type_1|UV-sensitive_syndrome_2|not_provided": 1,
    "Cockayne_syndrome_type_1|not_provided|Cockayne_syndrome|UV-sensitive_syndrome_2": 1,
    "UV-sensitive_syndrome_2|not_provided|Cockayne_syndrome_type_1|not_specified": 1,
    "not_specified|Cockayne_syndrome_type_1|not_provided": 1,
    "Cockayne_syndrome_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Cockayne_syndrome|Cockayne_syndrome_type_1|UV-sensitive_syndrome_2": 1,
    "not_provided|Abnormality_of_the_nervous_system|Cockayne_syndrome_type_1": 1,
    "Cockayne_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Cockayne_syndrome|UV-sensitive_syndrome_2|Cockayne_syndrome_type_1": 1,
    "Cockayne_syndrome_type_1|UV-sensitive_syndrome_2|ERCC8-related_disorder|not_provided": 1,
    "Cockayne_syndrome_type_1|Cockayne_syndrome|UV-sensitive_syndrome_2|not_provided": 1,
    "Cockayne_syndrome_type_1|Cockayne_syndrome|not_provided": 1,
    "not_provided|Cockayne_syndrome": 2,
    "Cockayne_syndrome|Mitochondrial_complex_I_deficiency|not_provided|Leigh_syndrome": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_10|not_provided": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_10": 10,
    "Cockayne_syndrome_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_10": 1,
    "Leigh_syndrome|Cockayne_syndrome_type_1|Mitochondrial_complex_I_deficiency": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_10": 2,
    "not_provided|Cockayne_syndrome|not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_10": 1,
    "Inborn_genetic_diseases|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 3,
    "not_specified|NDUFAF2-related_disorder|not_provided|Cockayne_syndrome_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_10": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases|Leigh_syndrome": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_10|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases|not_provided|not_specified|Leigh_syndrome": 1,
    "Leigh_syndrome|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_10|not_provided": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|not_specified|Leigh_syndrome": 1,
    "not_provided|not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_10": 1,
    "ZSWIM6-related_disorder|not_specified": 1,
    "not_provided|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features": 2,
    "Acromelic_frontonasal_dysostosis|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|not_provided": 4,
    "ZSWIM6-related_disorder": 14,
    "not_provided|Acromelic_frontonasal_dysostosis|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|Inborn_genetic_diseases": 1,
    "not_provided|Acromelic_frontonasal_dysostosis": 1,
    "ZSWIM6-related_disorder|not_provided": 9,
    "not_provided|ZSWIM6-related_disorder|not_specified": 1,
    "ZSWIM6-related_disorder|not_specified|not_provided": 3,
    "not_provided|not_specified|ZSWIM6-related_disorder": 1,
    "Acromelic_frontonasal_dysostosis|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Acromelic_frontonasal_dysostosis|not_provided": 2,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|Inborn_genetic_diseases": 1,
    "Acromelic_frontonasal_dysostosis": 5,
    "not_provided|ZSWIM6-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|ZSWIM6-related_disorder": 1,
    "not_provided|Acromelic_frontonasal_dysostosis|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features": 2,
    "Inborn_genetic_diseases|ZSWIM6-related_disorder|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|ZSWIM6-related_disorder|Acromelic_frontonasal_dysostosis|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|not_specified": 1,
    "Inborn_genetic_diseases|Acromelic_frontonasal_dysostosis": 1,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|Acromelic_frontonasal_dysostosis|not_provided": 1,
    "ZSWIM6-related_disorder|Acromelic_frontonasal_dysostosis|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features": 1,
    "Acromelic_frontonasal_dysostosis|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|ZSWIM6-related_disorder": 1,
    "Inborn_genetic_diseases|Acromelic_frontonasal_dysostosis|not_specified": 1,
    "Seizure|Intellectual_disability|Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Neurodevelopmental_disorder_with_movement_abnormalities|_abnormal_gait|_and_autistic_features|ZSWIM6-related_disorder|not_provided|ZSWIM6_related_intellectual_disability|Inborn_genetic_diseases": 1,
    "ZSWIM6-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|ZSWIM6-related_disorder|not_provided": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_3": 16,
    "KIF2A-related_disorder": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_3|not_provided": 3,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_3|not_specified": 1,
    "not_provided|KIF2A-related_disorder|not_specified": 1,
    "not_specified|KIF2A-related_disorder|not_provided": 1,
    "KIF2A-related_disorder|Inborn_genetic_diseases|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_3": 1,
    "KIF2A-related_disorder|not_provided": 3,
    "not_provided|KIF2A-related_disorder": 4,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_3": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_3|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_3|not_provided|Inborn_genetic_diseases": 1,
    "KIF2A-related_disorder|Complex_cortical_dysplasia_with_other_brain_malformations_3|not_provided|not_specified": 1,
    "Menstrual_cycle-dependent_periodic_fever": 1,
    "HTR1A-related_disorder": 1,
    "not_provided|Menstrual_cycle-dependent_periodic_fever": 1,
    "HTR1A-related_disorder|not_provided": 1,
    "Menstrual_cycle-dependent_periodic_fever|not_provided|not_specified": 1,
    "Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome|not_provided": 4,
    "not_provided|CWC27-related_disorder": 7,
    "Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome": 12,
    "not_provided|Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome": 5,
    "Retinitis_pigmentosa|not_provided|Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome": 1,
    "CWC27-related_disorder|not_provided": 5,
    "CWC27-related_disorder": 1,
    "not_provided|Retinal_dystrophy|Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome": 1,
    "Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Metaphyseal_chondrodysplasia-retinitis_pigmentosa_syndrome|Inborn_genetic_diseases": 1,
    "ADAMTS6-related_disorder": 4,
    "TRIM23-related_disorder": 2,
    "ERBIN-related_disorder|not_provided": 25,
    "ERBIN-related_disorder": 16,
    "not_provided|ERBIN-related_disorder": 16,
    "not_provided|not_specified|ERBIN-related_disorder": 2,
    "Amelia_cleft_lip_palate_hydrocephalus_iris_coloboma|not_provided": 1,
    "MAST-associated_epilepsy_syndrome": 1,
    "MAST4-associated_generalized_epilepsy": 1,
    "SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation": 135,
    "SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|not_provided": 7,
    "Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome": 109,
    "Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|not_specified": 1,
    "Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|PIK3R1-related_disorder": 1,
    "Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive": 15,
    "SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive": 55,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 58,
    "Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome": 14,
    "not_provided|PIK3R1-related_disorder|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive": 1,
    "Activated_PI3K-delta_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome": 2,
    "SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Activated_PI3K-delta_syndrome": 1,
    "not_provided|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive": 4,
    "Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|not_provided": 4,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|not_specified|not_provided": 5,
    "Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|not_provided": 1,
    "Agammaglobulinemia_7|_autosomal_recessive": 1,
    "not_provided|Activated_PI3K-delta_syndrome|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive": 1,
    "not_provided|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome": 1,
    "Activated_PI3K-delta_syndrome|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|not_specified": 1,
    "PIK3R1-related_disorder|not_provided|Inborn_genetic_diseases|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 1,
    "PIK3R1-related_disorder|not_provided|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|not_specified": 1,
    "not_provided|not_specified|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 1,
    "SHORT_syndrome": 17,
    "PIK3R1-related_disorder": 6,
    "Inborn_genetic_diseases|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome": 2,
    "not_specified|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome": 1,
    "SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|not_specified|not_provided": 1,
    "not_specified|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive": 3,
    "Activated_PI3K-delta_syndrome|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|not_provided": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|not_provided|not_specified": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|not_provided": 4,
    "Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|PIK3R1-related_disorder": 1,
    "Immunodeficiency_36_with_lymphoproliferation": 7,
    "Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|not_provided|Activated_PI3K-delta_syndrome": 1,
    "not_provided|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 4,
    "Inborn_genetic_diseases|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation": 1,
    "Inborn_genetic_diseases|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive": 1,
    "not_specified|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 1,
    "Inborn_genetic_diseases|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 1,
    "not_specified|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive": 1,
    "SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|not_provided": 2,
    "SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|PIK3R1-related_disorder": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Activated_PI3K-delta_syndrome": 2,
    "SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 1,
    "Multiple_congenital_anomalies/dysmorphic_syndrome|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|not_provided": 1,
    "Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "not_provided|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation": 2,
    "PIK3R1-related_disorder|SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation": 1,
    "Vascular_Malformations_and_Overgrowth": 5,
    "SHORT_syndrome|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|Activated_PI3K-delta_syndrome": 2,
    "Inherited_Immunodeficiency_Diseases|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation": 1,
    "Colorectal_cancer|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome": 1,
    "Vascular_malformation": 28,
    "Vascular_Malformations_and_Overgrowth|Overgrowth_syndrome": 1,
    "Inherited_Immunodeficiency_Diseases|Inborn_genetic_diseases|SHORT_syndrome|PIK3R1-related_disorder|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|not_provided|See_cases": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Inborn_genetic_diseases|not_specified|See_cases": 1,
    "Immunodeficiency_36_with_lymphoproliferation|not_provided": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome": 1,
    "Inborn_genetic_diseases|SHORT_syndrome": 1,
    "Vascular_Malformations_and_Overgrowth|Vascular_malformation": 1,
    "Vascular_Malformations_and_Overgrowth|CLOVES_syndrome": 2,
    "not_specified|Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|not_provided": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome|Immunodeficiency_36_with_lymphoproliferation|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Immunodeficiency_36_with_lymphoproliferation|Agammaglobulinemia_7|_autosomal_recessive|SHORT_syndrome": 1,
    "Agammaglobulinemia_7|_autosomal_recessive|Immunodeficiency_36_with_lymphoproliferation|SHORT_syndrome|not_provided": 1,
    "PIK3R1-related_disorder|not_specified|not_provided": 1,
    "Severe_hydrops_fetalis|Hydrops_fetalis|Noncompaction_cardiomyopathy|Concentric_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Recurrent_spontaneous_abortion": 4,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_49": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49": 44,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_49": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49|not_provided|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49|Rare_genetic_deafness": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_49": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_49|not_provided": 1,
    "MARVELD2-related_disorder|not_specified|not_provided": 1,
    "MARVELD2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_49|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49|not_provided": 7,
    "MARVELD2-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_49": 1,
    "not_provided|not_specified|MARVELD2-related_disorder": 1,
    "not_specified|MARVELD2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_49": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_49": 4,
    "not_provided|MARVELD2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_49": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_49|not_specified|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|not_specified": 1,
    "MARVELD2-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_49": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49|not_provided|Hearing_impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_49|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_49|not_specified": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_49|Ear_malformation": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_49": 1,
    "Pseudo-TORCH_syndrome_1": 22,
    "not_specified|not_provided|Pseudo-TORCH_syndrome_1": 1,
    "not_provided|OCLN-related_disorder|Pseudo-TORCH_syndrome_1": 1,
    "Pseudo-TORCH_syndrome_1|not_provided": 1,
    "not_provided|Pseudo-TORCH_syndrome_1": 1,
    "OCLN-related_disorder|not_specified|not_provided|Pseudo-TORCH_syndrome_1": 1,
    "not_provided|OCLN-related_disorder": 1,
    "Pseudo-TORCH_syndrome_1|Cerebral_calcification|Primary_microcephaly|Global_developmental_delay": 1,
    "Werdnig-Hoffmann_disease": 14,
    "Spinal_muscular_atrophy|not_specified|Kugelberg-Welander_disease|Spinal_muscular_atrophy|_modifier_of": 1,
    "Kugelberg-Welander_disease": 15,
    "not_provided|Kugelberg-Welander_disease|Spinal_muscular_atrophy|_type_II|Spinal_muscular_atrophy": 1,
    "Spinal_muscular_atrophy|_type_II": 9,
    "not_provided|Kugelberg-Welander_disease|Spinal_muscular_atrophy": 1,
    "Spinal_muscular_atrophy": 14,
    "Kugelberg-Welander_disease|Spinal_muscular_atrophy|_type_II|not_provided": 2,
    "not_provided|Spinal_muscular_atrophy|_type_II|Werdnig-Hoffmann_disease": 1,
    "Werdnig-Hoffmann_disease|not_provided": 2,
    "Kugelberg-Welander_disease|Werdnig-Hoffmann_disease": 1,
    "Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|_type_II|not_provided|Kugelberg-Welander_disease|Spinal_muscular_atrophy|_type_IV": 1,
    "not_provided|Spinal_muscular_atrophy|not_specified": 1,
    "Spinal_muscular_atrophy|not_specified|not_provided": 1,
    "not_provided|Werdnig-Hoffmann_disease": 3,
    "not_provided|Spinal_muscular_atrophy|Werdnig-Hoffmann_disease": 1,
    "Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|_type_IV|Spinal_muscular_atrophy|_type_II|Kugelberg-Welander_disease": 1,
    "not_provided|Kugelberg-Welander_disease": 1,
    "not_specified|Spinal_muscular_atrophy": 4,
    "Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|not_provided": 2,
    "not_provided|Spinal_muscular_atrophy|Spinal_muscular_atrophy|_type_IV": 1,
    "Werdnig-Hoffmann_disease|Spinal_muscular_atrophy": 1,
    "Spinal_muscular_atrophy|_type_II|Kugelberg-Welander_disease|Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|_type_IV|Spinal_muscular_atrophy": 1,
    "Spinal_muscular_atrophy|Kugelberg-Welander_disease": 1,
    "Spinal_muscular_atrophy|_type_II|Werdnig-Hoffmann_disease": 1,
    "not_provided|Spinal_muscular_atrophy": 1,
    "Spinal_muscular_atrophy|not_specified|Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|_type_IV|Spinal_muscular_atrophy|_type_II|Kugelberg-Welander_disease": 1,
    "Spinal_muscular_atrophy|not_provided": 2,
    "Spinal_muscular_atrophy|Inborn_genetic_diseases": 1,
    "not_specified|Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|_type_IV|Spinal_muscular_atrophy|_type_II|Kugelberg-Welander_disease": 1,
    "not_specified|Werdnig-Hoffmann_disease|Spinal_muscular_atrophy|_type_IV|Spinal_muscular_atrophy|_type_II|Kugelberg-Welander_disease|not_provided": 1,
    "Normal_pregnancy|Gestational_diabetes_mellitus_uncontrolled|Large_for_gestational_age": 1,
    "not_provided|not_specified|Hearing_loss|_autosomal_recessive_112": 3,
    "Hearing_loss|_autosomal_recessive_112": 6,
    "BDP1-related_disorder": 8,
    "not_provided|BDP1-related_disorder|not_specified": 2,
    "BDP1-related_disorder|not_provided": 3,
    "not_provided|BDP1-related_disorder": 12,
    "not_provided|Hearing_loss|_autosomal_recessive_112": 3,
    "Hearing_loss|_autosomal_recessive_112|not_provided|not_specified": 1,
    "BDP1-related_disorder|not_specified|not_provided": 1,
    "BDP1-related_disorder|not_specified": 1,
    "not_specified|not_provided|Hearing_loss|_autosomal_recessive_112": 6,
    "not_specified|Hearing_loss|_autosomal_recessive_112|not_provided": 1,
    "not_provided|not_specified|BDP1-related_disorder": 1,
    "not_specified|not_provided|Waardenburg_syndrome": 1,
    "not_specified|BDP1-related_disorder|not_provided": 2,
    "Hearing_loss|_autosomal_recessive_112|not_provided": 1,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 27,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_specified": 12,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency": 557,
    "Inborn_genetic_diseases|not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 5,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_provided": 16,
    "MCCC2-related_disorder|not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 2,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 12,
    "MCCC2-related_disorder|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 3,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 9,
    "MCCC2-related_disorder": 6,
    "not_specified|not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 4,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Inborn_genetic_diseases": 6,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 12,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|MCCC2-related_disorder": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|MCCC2-related_disorder": 6,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_provided|not_specified": 2,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|not_provided": 2,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_specified": 2,
    "not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|MCCC2-related_disorder|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "not_specified|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_specified|not_provided": 2,
    "MCCC2-related_disorder|3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|MCCC2-related_disorder": 2,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "Inborn_genetic_diseases|MCCC2-related_disorder|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "not_provided|not_specified|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Inborn_genetic_diseases|Methylcrotonyl-CoA_carboxylase_deficiency|not_specified": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Autism_spectrum_disorder": 1,
    "MCCC2-related_disorder|not_specified|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|not_specified|not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "MCCC2-related_disorder|Inborn_genetic_diseases|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency|See_cases": 1,
    "Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_provided|MCCC2-related_disorder|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|MCCC2-related_disorder|not_specified": 1,
    "not_provided|MCCC2-related_disorder": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_specified|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Inborn_genetic_diseases": 1,
    "Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency|not_provided": 3,
    "not_specified|3-methylcrotonyl-CoA_carboxylase_2_deficiency|MCCC2-related_disorder|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|MCCC2-related_disorder|Inborn_genetic_diseases|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Methylcrotonyl-CoA_carboxylase_deficiency|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Inborn_genetic_diseases|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency|MCCC2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|3-methylcrotonyl-CoA_carboxylase_2_deficiency": 1,
    "3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|not_specified": 2,
    "Spinal_muscular_atrophy|_type_IV": 1,
    "not_provided|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency|not_specified": 1,
    "MCCC2-related_disorder|3-methylcrotonyl-CoA_carboxylase_2_deficiency|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "MCCC2-related_disorder|Methylcrotonyl-CoA_carboxylase_deficiency": 1,
    "Obesity|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Periventricular_nodular_heterotopia_9": 38,
    "MAP1B-related_disorder": 56,
    "MAP1B-related_disorder|not_provided": 20,
    "not_provided|MAP1B-related_disorder": 11,
    "Periventricular_nodular_heterotopia_9|Hearing_loss|_autosomal_dominant_83": 8,
    "Periventricular_nodular_heterotopia": 4,
    "MAP1B-related_disorder|Periventricular_nodular_heterotopia_9|Hearing_loss|_autosomal_dominant_83": 1,
    "MAP1B-related_disorder|Periventricular_nodular_heterotopia_9|Periventricular_nodular_heterotopia|not_provided": 1,
    "Periventricular_nodular_heterotopia_9|Periventricular_nodular_heterotopia": 1,
    "Hearing_loss|_autosomal_dominant_83": 4,
    "Chromosome_5Q14.3_deletion_syndrome|_distal": 1,
    "White_matter_deficit|Periventricular_nodular_heterotopia|Cognitive_impairment|Hypoplasia_of_the_corpus_callosum|Periventricular_nodular_heterotopia_9": 1,
    "not_provided|Periventricular_nodular_heterotopia_9": 1,
    "Periventricular_nodular_heterotopia_9|Inborn_genetic_diseases": 4,
    "MAP1B-related_disorder|not_specified|not_provided": 1,
    "MAP1B-related_disorder|Inborn_genetic_diseases": 4,
    "not_provided|Periventricular_nodular_heterotopia_9|Hearing_loss|_autosomal_dominant_83": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_dominant_83|Periventricular_nodular_heterotopia_9": 1,
    "Autism_spectrum_disorder|White_matter_deficit|Periventricular_nodular_heterotopia|Cognitive_impairment|Hypoplasia_of_the_corpus_callosum|Periventricular_nodular_heterotopia_9": 1,
    "Periventricular_nodular_heterotopia_9|not_provided|Periventricular_nodular_heterotopia": 1,
    "not_specified|MAP1B-related_disorder": 1,
    "Inborn_genetic_diseases|MAP1B-related_disorder": 6,
    "Periventricular_nodular_heterotopia_9|Periventricular_cysts|Macrocephaly": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_dominant_83": 1,
    "MAP1B-related_disorder|Hearing_loss|_autosomal_dominant_83|Periventricular_nodular_heterotopia_9|not_provided": 1,
    "Neurodevelopmental_disorder|not_provided|Periventricular_nodular_heterotopia_9|Autism_spectrum_disorder|White_matter_deficit|Hypoplasia_of_the_corpus_callosum|Cognitive_impairment|Periventricular_nodular_heterotopia": 1,
    "Hearing_loss|_autosomal_dominant_83|Periventricular_nodular_heterotopia_9|MAP1B-related_disorder|not_provided": 1,
    "Periventricular_nodular_heterotopia_9|Attention_deficit_hyperactivity_disorder|Metopic_synostosis|Abnormal_facial_shape|Global_developmental_delay|Hypotonia|Pyloric_stenosis": 1,
    "Hearing_loss|_autosomal_dominant_83|Periventricular_nodular_heterotopia_9": 1,
    "MAP1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Periventricular_nodular_heterotopia_9": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_83": 1,
    "Hearing_loss|_autosomal_dominant_83|Periventricular_nodular_heterotopia_9|Inborn_genetic_diseases|MAP1B-related_disorder": 1,
    "TNPO1-related_disorder": 13,
    "FOXD1-related_disorder": 29,
    "not_specified|FOXD1-related_disorder": 1,
    "ARHGEF28-related_disorder": 90,
    "not_specified|ARHGEF28-related_disorder": 13,
    "ARHGEF28-related_disorder|not_provided": 6,
    "ARHGEF28-related_disorder|not_specified": 8,
    "not_provided|ARHGEF28-related_disorder": 2,
    "not_provided|not_specified|ARHGEF28-related_disorder": 1,
    "not_specified|Meniere_disease|ARHGEF28-related_disorder": 1,
    "Meniere_disease|ARHGEF28-related_disorder": 1,
    "not_provided|ARHGEF28-related_disorder|Meniere_disease": 1,
    "Meniere_disease|not_specified": 2,
    "ENC1-related_disorder": 1,
    "Sandhoff_disease|not_provided": 18,
    "not_provided|Sandhoff_disease": 21,
    "Sandhoff_disease": 657,
    "Sandhoff_disease|Inborn_genetic_diseases": 11,
    "Sandhoff_disease|_infantile_form|Sandhoff_disease": 2,
    "Inborn_genetic_diseases|Sandhoff_disease": 9,
    "not_specified|not_provided|Sandhoff_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Sandhoff_disease|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Sandhoff_disease": 2,
    "Sandhoff_disease|not_provided|not_specified": 1,
    "HEXB-related_disorder|not_specified|not_provided|Sandhoff_disease": 1,
    "Sandhoff_disease|not_provided|HEXB-related_disorder": 1,
    "not_provided|not_specified|Sandhoff_disease": 3,
    "not_provided|Sandhoff_disease|Inborn_genetic_diseases": 1,
    "Sandhoff_disease|not_specified|HEXB_POLYMORPHISM|not_provided": 1,
    "Sandhoff_disease|HEXB-related_disorder|not_provided": 1,
    "not_specified|not_provided|Sandhoff_disease": 4,
    "not_provided|Sandhoff_disease|not_specified": 3,
    "not_specified|Sandhoff_disease|HEXB_POLYMORPHISM|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Sandhoff_disease": 1,
    "not_specified|Sandhoff_disease": 7,
    "Sandhoff_disease|not_specified|not_provided": 1,
    "Sandhoff_disease|not_provided|Inborn_genetic_diseases": 1,
    "See_cases|Sandhoff_disease": 1,
    "not_provided|Sandhoff_disease|See_cases": 1,
    "Sandhoff_disease|_infantile_form|not_provided|Sandhoff_disease": 1,
    "Sandhoff_disease|Sandhoff_disease|_infantile_form": 1,
    "Sandhoff_disease|not_specified": 1,
    "Sandhoff_disease|_infantile_form": 1,
    "not_specified|HEXB-related_disorder|Sandhoff_disease": 1,
    "HEXB-related_disorder|Inborn_genetic_diseases|not_provided|Sandhoff_disease|_juvenile_form|Sandhoff_disease|_adult_form|Sandhoff_disease|See_cases": 1,
    "Sandhoff_disease|HEXB-related_disorder": 1,
    "Sandhoff_disease|Sandhoff_disease|_juvenile_form|not_provided|not_specified": 1,
    "Sandhoff_disease|Inborn_genetic_diseases|not_provided": 1,
    "Sandhoff_disease|_adult_form": 1,
    "HEXB-related_disorder|Sandhoff_disease": 1,
    "not_provided|Sandhoff_disease|Sandhoff_disease|_juvenile_form|Inborn_genetic_diseases": 1,
    "HEXB-related_disorder": 2,
    "Sandhoff_disease|not_provided|Sandhoff_disease|_chronic": 1,
    "Sandhoff_disease|Sandhoff_disease|_adult_form": 1,
    "not_provided|Hexosaminidase_B_(Paris)|Sandhoff_disease": 1,
    "not_provided|HEXOSAMINIDASE_B|_HEAT-LABILE_POLYMORPHISM|Sandhoff_disease": 1,
    "HEXB-related_disorder|not_provided|Sandhoff_disease": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_deficiency_39": 1,
    "GFM2-related_disorder|not_specified|not_provided": 2,
    "Combined_oxidative_phosphorylation_deficiency_39": 12,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Combined_oxidative_phosphorylation_deficiency_39|Inborn_genetic_diseases|not_provided": 1,
    "GFM2-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_39|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_39|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_39|not_provided": 3,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_39": 3,
    "GFM2-related_disorder": 7,
    "not_provided|Inborn_genetic_diseases|GFM2-related_disorder": 1,
    "not_provided|GFM2-related_disorder": 2,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Combined_oxidative_phosphorylation_deficiency_39|not_provided": 1,
    "not_provided|not_specified|GFM2-related_disorder": 1,
    "not_provided|GFM2-related_disorder|not_specified": 1,
    "Mitochondrial_disease|Combined_oxidative_phosphorylation_deficiency_39": 2,
    "Hepatoencephalopathy_due_to_combined_oxidative_phosphorylation_defect_type_1|Combined_oxidative_phosphorylation_deficiency_39|Mitochondrial_disease|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_39|not_specified|not_provided": 2,
    "not_specified|ANKRD31-related_disorder": 2,
    "ANKRD31-related_disorder": 2,
    "not_provided|not_specified|ANKRD31-related_disorder": 1,
    "Inherited_primary_ovarian_failure": 2,
    "HMGCR-related_disorder": 6,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_28": 4,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_28": 2,
    "Low_density_lipoprotein_cholesterol_level_quantitative_trait_locus_3": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_28|Basal_cell_nevus_syndrome_1": 1,
    "Statins|_attenuated_cholesterol_lowering_by": 6,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_28|Limb-girdle_muscular_dystrophy": 1,
    "COL4A3BP-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_34": 23,
    "CERT1-related_disorder": 9,
    "Intellectual_disability|_autosomal_dominant_34|Inborn_genetic_diseases": 3,
    "CERT1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_34": 1,
    "not_provided|CERT1-related_disorder": 2,
    "Intellectual_disability|_autosomal_dominant_34|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_34": 1,
    "CERT1-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Microcephaly|Spastic_paraparesis|Neurodevelopmental_abnormality": 1,
    "Intellectual_disability|_autosomal_dominant_34|Intellectual_disability|not_provided": 1,
    "Prostate_cancer|Seizure|Neurodevelopmental_delay": 1,
    "Scoliosis|not_provided": 3,
    "Retinal_dystrophy|POC5-related_disorder|not_specified|not_provided": 1,
    "not_provided|POC5-related_disorder": 1,
    "not_provided|Retinal_dystrophy|Optic_atrophy": 1,
    "Syndromic_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa": 1,
    "SV2C-related_disorder": 13,
    "SV2C-related_disorder|not_provided": 1,
    "F2R-related_disorder": 1,
    "Non-syndromic_syndactyly": 2,
    "Autosomal_dominant_striatal_neurodegeneration_type_1": 47,
    "Autosomal_dominant_striatal_neurodegeneration_type_1|not_provided": 29,
    "Autosomal_dominant_striatal_neurodegeneration_type_1|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_striatal_neurodegeneration_type_1": 8,
    "Autosomal_dominant_striatal_neurodegeneration_type_1|Inborn_genetic_diseases": 2,
    "PDE8B-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_striatal_neurodegeneration_type_1": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_striatal_neurodegeneration_type_1": 2,
    "PDE8B-Related_Disorders": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_3": 1,
    "Autosomal_dominant_striatal_neurodegeneration_type_1|PDE8B-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_striatal_neurodegeneration_type_1|not_provided": 1,
    "not_specified|Autosomal_dominant_striatal_neurodegeneration_type_1|PDE8B-related_disorder|not_provided": 1,
    "not_provided|PDE8B-related_disorder": 2,
    "PDE8B-related_disorder": 3,
    "PDE8B-related_disorder|not_provided|Autosomal_dominant_striatal_neurodegeneration_type_1": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_striatal_neurodegeneration_type_1|not_provided|PDE8B-related_disorder": 1,
    "Autosomal_dominant_striatal_neurodegeneration_type_1|Striatal_Degeneration|not_provided": 2,
    "Striatal_Degeneration": 9,
    "not_provided|Striatal_Degeneration": 1,
    "Hermansky-Pudlak_syndrome_2": 611,
    "not_specified|Hermansky-Pudlak_syndrome|not_provided": 2,
    "Hermansky-Pudlak_syndrome_2|not_provided": 10,
    "AP3B1-related_disorder": 3,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|Hermansky-Pudlak_syndrome_2": 1,
    "not_specified|Hermansky-Pudlak_syndrome_2|not_provided": 2,
    "Hermansky-Pudlak_syndrome_2|Autoinflammatory_syndrome": 2,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_2": 20,
    "Hermansky-Pudlak_syndrome_2|Inborn_genetic_diseases": 21,
    "Hermansky-Pudlak_syndrome_2|not_specified|Autoinflammatory_syndrome|not_provided|Hermansky-Pudlak_syndrome": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_2": 4,
    "AP3B1-related_disorder|not_specified|Hermansky-Pudlak_syndrome_2": 1,
    "not_specified|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome|AP3B1-related_disorder|Hermansky-Pudlak_syndrome_2": 1,
    "not_specified|Autoinflammatory_syndrome|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_2": 1,
    "Autoinflammatory_syndrome|Hermansky-Pudlak_syndrome_2|not_provided": 1,
    "not_specified|not_provided|AP3B1-related_disorder|Inborn_genetic_diseases|Combined_immunodeficiency|Hermansky-Pudlak_syndrome_2": 1,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_2": 2,
    "Autoinflammatory_syndrome|not_specified|Hermansky-Pudlak_syndrome_2|not_provided": 2,
    "not_specified|Hermansky-Pudlak_syndrome_2": 13,
    "not_provided|Hermansky-Pudlak_syndrome_2|Inborn_genetic_diseases": 1,
    "AP3B1-related_disorder|not_specified|Autoinflammatory_syndrome|not_provided|Hermansky-Pudlak_syndrome_2": 1,
    "Hermansky-Pudlak_syndrome_2|not_specified": 6,
    "Hermansky-Pudlak_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Hermansky-Pudlak_syndrome_2|AP3B1-related_disorder": 3,
    "Hermansky-Pudlak_syndrome_2|not_specified|AP3B1-related_disorder": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_2|Autoinflammatory_syndrome|not_specified|not_provided": 1,
    "not_provided|Hermansky-Pudlak_syndrome_2": 4,
    "Hermansky-Pudlak_syndrome_2|not_specified|not_provided": 2,
    "Autoinflammatory_syndrome|not_specified|not_provided|Hermansky-Pudlak_syndrome_2": 3,
    "not_specified|Hermansky-Pudlak_syndrome_2|AP3B1-related_disorder": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_2|AP3B1-related_disorder|Abnormal_bleeding|Thrombocytopenia": 1,
    "AP3B1-related_disorder|Hermansky-Pudlak_syndrome_2": 3,
    "AP3B1-related_disorder|not_provided|Autoinflammatory_syndrome|Hermansky-Pudlak_syndrome_2": 1,
    "Intellectual_disability|Hermansky-Pudlak_syndrome_2": 1,
    "Hermansky-Pudlak_syndrome_2|not_provided|Inborn_genetic_diseases": 3,
    "Hermansky-Pudlak_syndrome_2|Hermansky-Pudlak_syndrome|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Hermansky-Pudlak_syndrome_2": 4,
    "Hermansky-Pudlak_syndrome|not_specified|not_provided|Hermansky-Pudlak_syndrome_2": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_2|not_specified": 2,
    "not_specified|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_2": 1,
    "not_provided|AP3B1-related_disorder|not_specified|Hermansky-Pudlak_syndrome_2": 1,
    "Hermansky-Pudlak_syndrome_2|Hermansky-Pudlak_syndrome|not_provided|not_specified": 1,
    "Hermansky-Pudlak_syndrome_2|AP3B1-related_disorder|not_specified": 1,
    "Hermansky-Pudlak_syndrome_2|not_specified|AP3B1-related_disorder|not_provided": 1,
    "Hermansky-Pudlak_syndrome|not_provided|Hermansky-Pudlak_syndrome_2|not_specified|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|Prostate_cancer|Hermansky-Pudlak_syndrome_2": 1,
    "Hermansky-Pudlak_syndrome_2|not_provided|AP3B1-related_disorder": 1,
    "not_specified|AP3B1-related_disorder|Autoinflammatory_syndrome|not_provided|Hermansky-Pudlak_syndrome_2": 1,
    "Hermansky-Pudlak_syndrome_2|AP3B1-related_disorder|Autoinflammatory_syndrome": 1,
    "Hermansky-Pudlak_syndrome_2|not_provided|Hermansky-Pudlak_syndrome|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|AP3B1-related_disorder|not_specified|not_provided|Hermansky-Pudlak_syndrome_2": 1,
    "not_specified|Hermansky-Pudlak_syndrome_2|Autoinflammatory_syndrome|not_provided": 2,
    "not_specified|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_2|not_provided": 2,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_2": 3,
    "not_specified|Hermansky-Pudlak_syndrome_2|Autoinflammatory_syndrome": 1,
    "Hermansky-Pudlak_syndrome_2|Hermansky-Pudlak_syndrome": 1,
    "not_specified|Hermansky-Pudlak_syndrome_2|not_provided|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|AP3B1-related_disorder|Hermansky-Pudlak_syndrome_2": 1,
    "not_provided|Mucopolysaccharidosis_type_6": 32,
    "Mucopolysaccharidosis_type_6": 810,
    "Mucopolysaccharidosis_type_6|not_provided": 27,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_6": 9,
    "ARSB-related_disorder|Mucopolysaccharidosis_type_6": 3,
    "not_specified|Mucopolysaccharidosis_type_6": 4,
    "Mucopolysaccharidosis_type_6|not_specified": 9,
    "not_provided|ARSB-related_disorder|Mucopolysaccharidosis_type_6": 1,
    "Mucopolysaccharidosis_type_6|Inborn_genetic_diseases": 8,
    "Mucopolysaccharidosis_type_6|Mucopolysaccharidosis|_type_vi|_severe|not_provided|Metachromatic_leukodystrophy": 1,
    "Mucopolysaccharidosis_type_6|not_provided|not_specified": 4,
    "Mucopolysaccharidosis_type_6|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Mucopolysaccharidosis_type_6": 3,
    "not_provided|not_specified|Mucopolysaccharidosis_type_6": 2,
    "Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis_type_6": 1,
    "ARSB-related_disorder|not_provided|Mucopolysaccharidosis_type_6": 1,
    "Mucopolysaccharidosis_type_6|ARSB-related_disorder|not_provided": 1,
    "Mucopolysaccharidosis_type_6|Mucopolysaccharidosis|_type_vi|_severe": 3,
    "Mucopolysaccharidosis_type_6|Mucopolysaccharidosis|_type_vi|_mild": 1,
    "not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis_type_6": 1,
    "ARSB-related_disorder|not_provided|Metachromatic_leukodystrophy|Mucopolysaccharidosis_type_6": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_6|not_provided": 2,
    "Mucopolysaccharidosis_type_6|Mucopolysaccharidosis|_type_vi|_intermediate": 1,
    "not_provided|Mucopolysaccharidosis_type_6|See_cases": 1,
    "Mucopolysaccharidosis_type_6|ARSB-related_disorder": 2,
    "not_provided|Mucopolysaccharidosis_type_6|not_specified": 1,
    "ARSB-related_disorder|not_specified|not_provided|Mucopolysaccharidosis_type_6": 1,
    "not_provided|Mucopolysaccharidosis_type_6|ARSB-related_disorder": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_6|See_cases": 1,
    "not_specified|not_provided|DMGDH-related_disorder": 1,
    "DMGDH-related_disorder": 7,
    "not_provided|DMGDH-related_disorder|not_specified": 1,
    "Dimethylglycine_dehydrogenase_deficiency": 4,
    "DMGDH-related_disorder|not_specified": 1,
    "Dimethylglycine_dehydrogenase_deficiency|not_provided": 2,
    "not_specified|DMGDH-related_disorder|not_provided": 1,
    "not_provided|Dimethylglycine_dehydrogenase_deficiency": 2,
    "Dimethylglycine_dehydrogenase_deficiency|not_specified": 1,
    "BHMT-related_disorder": 1,
    "Constitutional_megaloblastic_anemia_with_severe_neurologic_disease": 5,
    "not_provided|DHFR-related_disorder": 1,
    "DHFR-related_disorder|not_provided": 1,
    "Familial_adenomatous_polyposis_4": 110,
    "not_provided|Familial_adenomatous_polyposis_4|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 54,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_specified": 1,
    "not_specified|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 29,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Endometrial_carcinoma": 1,
    "Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome": 15,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 38,
    "Endometrial_carcinoma|not_provided|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 10,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|MSH3-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_4|MSH3-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided|Endometrial_carcinoma": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|MSH3-related_disorder": 6,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|not_provided": 15,
    "MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|MSH3-related_disorder|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Constitutional_megaloblastic_anemia_with_severe_neurologic_disease|Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 1,
    "not_provided|Familial_adenomatous_polyposis_4|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 8,
    "not_specified|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 4,
    "not_specified|Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Constitutional_megaloblastic_anemia_with_severe_neurologic_disease|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 3,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 12,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided": 6,
    "Familial_adenomatous_polyposis_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Constitutional_megaloblastic_anemia_with_severe_neurologic_disease|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_4|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|not_specified|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_4|Inborn_genetic_diseases|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Familial_adenomatous_polyposis_4": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided": 9,
    "not_provided|Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_provided": 3,
    "not_provided|not_specified|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 33,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided": 15,
    "not_provided|Endometrial_carcinoma|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|Endometrial_carcinoma|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 5,
    "MSH3-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 9,
    "MSH3-related_disorder|not_provided": 4,
    "not_provided|Familial_adenomatous_polyposis_4": 22,
    "Familial_adenomatous_polyposis_4|not_provided": 20,
    "not_provided|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 19,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 7,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 1,
    "Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 1,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided": 18,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|not_provided|Endometrial_carcinoma": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_4": 12,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome": 14,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 1,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 11,
    "not_specified|MSH3-related_disorder|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided|MSH3-related_disorder": 2,
    "not_provided|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_specified|MSH3-related_disorder|not_provided": 1,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_specified": 1,
    "Endometrial_carcinoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|MSH3-related_disorder": 1,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_provided": 1,
    "MSH3-related_disorder|Familial_adenomatous_polyposis_4|not_provided": 1,
    "Familial_adenomatous_polyposis_4|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "MSH3-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_specified|not_provided": 1,
    "MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "not_specified|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|not_specified|Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 1,
    "not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 2,
    "Familial_adenomatous_polyposis_4|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Familial_adenomatous_polyposis_4": 5,
    "Familial_adenomatous_polyposis_4|MSH3-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 5,
    "MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Familial_adenomatous_polyposis_4": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_4|not_provided": 1,
    "Familial_adenomatous_polyposis_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_specified|not_provided": 1,
    "MSH3-related_disorder|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 8,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|MSH3-related_disorder|Endometrial_carcinoma|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder": 3,
    "MSH3-related_disorder|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Endometrial_carcinoma|MSH3-related_disorder|Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4": 7,
    "not_specified|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|Familial_adenomatous_polyposis_4|not_provided|Endometrial_carcinoma": 1,
    "not_specified|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|MSH3-related_disorder|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Endometrial_carcinoma|not_provided": 1,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided|MSH3-related_disorder": 1,
    "Familial_adenomatous_polyposis_4|not_specified|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_4|not_provided|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_specified|not_provided|MSH3-related_disorder": 1,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|MSH3-related_disorder": 1,
    "Familial_adenomatous_polyposis_4|not_provided|Endometrial_carcinoma": 1,
    "not_specified|not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 3,
    "Endometrial_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|MSH3-related_disorder|Familial_adenomatous_polyposis_4": 1,
    "MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_4": 1,
    "MSH3-related_disorder|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|not_specified|not_provided|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_specified|Familial_adenomatous_polyposis_4|not_provided": 1,
    "Familial_adenomatous_polyposis_4|MSH3-related_disorder|Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|Familial_adenomatous_polyposis_4|not_provided|Endometrial_carcinoma|not_specified": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|MSH3-related_disorder|Familial_adenomatous_polyposis_4": 1,
    "not_provided|MSH3-related_disorder": 3,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_4": 2,
    "not_provided|Endometrial_carcinoma|MSH3-related_disorder|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided|not_specified": 1,
    "Endometrial_carcinoma|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|not_provided": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|not_provided|Familial_adenomatous_polyposis_4": 1,
    "not_provided|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|not_provided|MSH3-related_disorder|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|MSH3-related_disorder|Familial_adenomatous_polyposis_4|not_provided": 1,
    "MSH3-related_disorder|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|not_specified|not_provided|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|MSH3-related_disorder|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Diffuse_midline_glioma|_H3_K27-altered": 1,
    "Familial_adenomatous_polyposis_4|not_provided|not_specified|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_4": 1,
    "Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_provided|MSH3-related_disorder|not_specified|Endometrial_carcinoma": 1,
    "not_provided|Endometrial_carcinoma|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "MSH3-related_disorder|Familial_adenomatous_polyposis_4|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_4|Endometrial_carcinoma": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder": 1,
    "Familial_adenomatous_polyposis_4|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|MSH3-related_disorder": 1,
    "not_specified|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided": 1,
    "not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Familial_adenomatous_polyposis_4|MSH3-related_disorder|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|Endometrial_carcinoma|not_specified|Familial_adenomatous_polyposis_4": 1,
    "MSH3-related_disorder|not_provided|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_4": 1,
    "MSH3-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "MSH3-related_disorder|not_provided|not_specified": 1,
    "Endometrial_carcinoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Diffuse_midline_glioma|_H3_K27-altered|Endometrial_carcinoma": 1,
    "Endometrial_carcinoma|MSH3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Endometrial_carcinoma|MSH3-related_disorder|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome": 1,
    "MSH3-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|MSH3-related_disorder": 1,
    "Endometrial_carcinoma|Familial_adenomatous_polyposis_4|Hereditary_cancer-predisposing_syndrome|MSH3-related_disorder|not_provided": 1,
    "MSH3-related_disorder|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MSH3-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma": 1,
    "not_provided|MSH3-related_disorder|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|MSH3-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Familial_adenomatous_polyposis_4|not_specified": 1,
    "Brachycephaly|_trichomegaly|_and_developmental_delay": 4,
    "Brachycephaly|_trichomegaly|_and_developmental_delay|not_provided": 1,
    "Short_stature|_microcephaly|_and_endocrine_dysfunction": 34,
    "Short_stature|_microcephaly|_and_endocrine_dysfunction|not_provided": 7,
    "not_provided|Short_stature|_microcephaly|_and_endocrine_dysfunction": 12,
    "Short_stature|_microcephaly|_and_endocrine_dysfunction|not_provided|Inborn_genetic_diseases": 2,
    "Short_stature|_microcephaly|_and_endocrine_dysfunction|not_provided|Ateleiotic_dwarfism|XRCC4-related_disorder": 1,
    "Inborn_genetic_diseases|Short_stature|_microcephaly|_and_endocrine_dysfunction|not_provided": 1,
    "Inborn_genetic_diseases|Short_stature|_microcephaly|_and_endocrine_dysfunction": 2,
    "Short_stature|_microcephaly|_and_endocrine_dysfunction|Inborn_genetic_diseases": 3,
    "XRCC4-related_disorder|Short_stature|_microcephaly|_and_endocrine_dysfunction|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Short_stature|_microcephaly|_and_endocrine_dysfunction": 1,
    "Vitreoretinopathy|Wagner_disease": 9,
    "Wagner_disease|Vitreoretinopathy": 64,
    "Wagner_disease|VCAN-related_disorder|not_provided|Inborn_genetic_diseases|Vitreoretinopathy": 1,
    "Wagner_disease|Vitreoretinopathy|Inborn_genetic_diseases|not_provided": 2,
    "Vitreoretinopathy|not_provided|Wagner_disease": 13,
    "not_provided|Wagner_disease|Vitreoretinopathy": 32,
    "not_specified|Wagner_disease|Vitreoretinopathy|not_provided": 3,
    "Vitreoretinopathy|not_specified|not_provided|Wagner_disease": 4,
    "VCAN-related_disorder|not_provided": 22,
    "not_specified|not_provided|Vitreoretinopathy|Wagner_disease": 6,
    "not_provided|VCAN-related_disorder": 16,
    "Wagner_disease|VCAN-related_disorder|Retinal_dystrophy|not_provided|Inborn_genetic_diseases|Vitreoretinopathy": 1,
    "Inborn_genetic_diseases|not_provided|Wagner_disease|Vitreoretinopathy": 2,
    "Wagner_disease|not_provided|Vitreoretinopathy": 4,
    "not_provided|Wagner_disease|Inborn_genetic_diseases|Vitreoretinopathy": 2,
    "VCAN-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "VCAN-related_disorder|not_provided|not_specified": 2,
    "VCAN-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Wagner_disease|VCAN-related_disorder|Vitreoretinopathy": 1,
    "VCAN-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Wagner_disease": 1,
    "not_provided|Wagner_disease": 9,
    "VCAN-related_disorder": 12,
    "not_specified|not_provided|Wagner_disease|Vitreoretinopathy": 7,
    "Vitreoretinopathy|VCAN-related_disorder|not_provided|Inborn_genetic_diseases|Wagner_disease": 2,
    "Wagner_disease|Vitreoretinopathy|not_provided": 13,
    "not_provided|not_specified|Vitreoretinopathy|Wagner_disease": 2,
    "not_provided|Inborn_genetic_diseases|Wagner_disease|Vitreoretinopathy": 2,
    "Wagner_disease": 16,
    "not_provided|Wagner_disease|Inborn_genetic_diseases|Vitreoretinopathy|VCAN-related_disorder": 1,
    "Inborn_genetic_diseases|VCAN-related_disorder|not_specified|not_provided": 1,
    "not_provided|Wagner_disease|VCAN-related_disorder|Vitreoretinopathy|Inborn_genetic_diseases": 1,
    "not_provided|VCAN-related_disorder|Inborn_genetic_diseases": 3,
    "Wagner_disease|not_provided": 7,
    "not_provided|Wagner_disease|not_specified|Vitreoretinopathy": 1,
    "Inborn_genetic_diseases|VCAN-related_disorder|not_provided": 3,
    "Vitreoretinopathy|VCAN-related_disorder|not_provided|Wagner_disease": 1,
    "not_provided|Inborn_genetic_diseases|Wagner_disease|Vitreoretinopathy|not_specified": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Wagner_disease": 1,
    "Stickler_syndrome|Wagner_disease": 1,
    "Wagner_disease|Retinitis_pigmentosa|Premature_loss_of_teeth|Congenital_heart_disease|Retinal_dystrophy|not_provided": 1,
    "Vitreoretinopathy|Wagner_disease|not_provided": 12,
    "Wagner_disease|Vitreoretinopathy|not_specified|not_provided": 3,
    "VCAN-related_disorder|Inborn_genetic_diseases|not_provided": 7,
    "not_provided|Vitreoretinopathy|not_specified|Wagner_disease": 2,
    "not_provided|Wagner_disease|Vitreoretinopathy|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Wagner_disease|Vitreoretinopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|VCAN-related_disorder": 4,
    "not_provided|Vitreoretinopathy|Wagner_disease": 2,
    "Vitreoretinopathy|not_provided|Wagner_disease|Inborn_genetic_diseases": 1,
    "VCAN-related_disorder|not_provided|Vitreoretinopathy|Inborn_genetic_diseases|Wagner_disease": 2,
    "VCAN-related_disorder|not_provided|Wagner_disease|Vitreoretinopathy": 3,
    "Inborn_genetic_diseases|Wagner_disease|not_provided": 1,
    "Vitreoretinopathy|not_specified|Wagner_disease|not_provided": 2,
    "Vitreoretinopathy|Wagner_disease|Inborn_genetic_diseases|not_provided": 4,
    "Wagner_disease|Vitreoretinopathy|Inborn_genetic_diseases": 3,
    "Vitreoretinopathy|VCAN-related_disorder|Wagner_disease|not_provided": 1,
    "Wagner_disease|Retinitis_pigmentosa|not_provided|Vitreoretinopathy": 1,
    "not_provided|Wagner_disease|Vitreoretinopathy|not_specified": 3,
    "Vitreoretinopathy|VCAN-related_disorder|Wagner_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|VCAN-related_disorder|not_specified|Wagner_disease|Vitreoretinopathy": 1,
    "not_provided|Vitreoretinopathy|Wagner_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Wagner_disease": 1,
    "Inborn_genetic_diseases|Wagner_disease|Vitreoretinopathy|not_provided": 1,
    "not_provided|Vitreoretinopathy|Wagner_disease|not_specified": 1,
    "Wagner_disease|not_provided|Vitreoretinopathy|not_specified": 1,
    "not_specified|Vitreoretinopathy|Wagner_disease|not_provided": 1,
    "Vitreoretinopathy|Inborn_genetic_diseases|not_specified|Wagner_disease|not_provided": 1,
    "Wagner_disease|Inborn_genetic_diseases|not_provided|Vitreoretinopathy": 1,
    "VCAN-related_disorder|Wagner_disease|Vitreoretinopathy|not_provided": 1,
    "not_specified|Vitreoretinopathy|not_provided|Wagner_disease": 1,
    "Wagner_disease|Inborn_genetic_diseases": 1,
    "Wagner_disease|not_provided|Inborn_genetic_diseases": 1,
    "Wagner_disease|VCAN-related_disorder|Vitreoretinopathy": 1,
    "Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome": 7,
    "RASA1-related_disorder": 10,
    "Capillary_malformation-arteriovenous_malformation_syndrome": 813,
    "Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome": 8,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|not_provided": 8,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype": 79,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome": 107,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1": 10,
    "Capillary_malformation-arteriovenous_malformation_syndrome|not_provided|Capillary_malformation-arteriovenous_malformation_1": 3,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1|RASA1-related_disorder": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_syndrome": 17,
    "Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|RASA1-related_disorder|Cardiovascular_phenotype": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided|Capillary_malformation-arteriovenous_malformation_1": 1,
    "RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|not_provided|Parkes_Weber_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1|Cardiovascular_phenotype|not_specified|not_provided|Parkes_Weber_syndrome": 1,
    "Cardiovascular_phenotype|RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1": 11,
    "Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1|Cardiovascular_phenotype|not_provided|Capillary_malformation-arteriovenous_malformation_syndrome|Parkes_Weber_syndrome": 1,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1": 1,
    "RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype": 3,
    "Capillary_malformation-arteriovenous_malformation_syndrome|RASA1-related_disorder|Cardiovascular_phenotype": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|Parkes_Weber_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Capillary_malformation-arteriovenous_malformation_syndrome": 2,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1|Gorham-Stout_disease|not_provided": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_1": 2,
    "Angioosteohypertrophic_syndrome": 3,
    "not_provided|Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "not_provided|Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_1": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 19,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_1": 1,
    "not_provided|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Wieacker-Wolff_syndrome": 23,
    "Vascular_malformation|RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided|Capillary_malformation-arteriovenous_malformation_1": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_1": 3,
    "Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|RASA1-related_disorder": 1,
    "Capillary_malformation": 2,
    "not_provided|Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_1": 2,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_1": 1,
    "Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_syndrome|RASA1-related_disorder": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|not_specified": 3,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|RASA1-related_disorder|not_provided": 2,
    "not_provided|Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1": 1,
    "RASA1-related_disorder|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_1|RASA1-related_disorder|Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "not_specified|Capillary_malformation-arteriovenous_malformation_syndrome": 3,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|RASA1-related_disorder": 1,
    "not_specified|not_provided|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "not_specified|Capillary_malformation-arteriovenous_malformation_1|RASA1-related_disorder|Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|RASA1-related_disorder": 3,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|RASA1-related_disorder": 1,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 3,
    "Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|not_specified|Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome": 1,
    "Hydrops_fetalis|Cerebral_venous_angioma": 1,
    "Vascular_malformation|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|Parkes_Weber_syndrome": 3,
    "Capillary_malformation-arteriovenous_malformation_1|RASA1-related_disorder": 1,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Cardiovascular_phenotype|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_1": 2,
    "not_specified|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Capillary_malformation-arteriovenous_malformation_syndrome": 2,
    "not_provided|Vascular_malformation|RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 2,
    "RASA1-related_disorder|not_provided|Capillary_malformation-arteriovenous_malformation_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Capillary_malformation-arteriovenous_malformation_1|not_provided": 1,
    "RASA1-related_disorder|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided|Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|not_provided": 2,
    "Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|not_provided|RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_1": 1,
    "Capillary_malformation-arteriovenous_malformation_1|RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Capillary_malformation-arteriovenous_malformation_syndrome|Cardiovascular_phenotype": 1,
    "RASA1-related_disorder|Capillary_malformation-arteriovenous_malformation_syndrome|Hereditary_hemorrhagic_telangiectasia": 1,
    "Capillary_malformation-arteriovenous_malformation_syndrome|Capillary_malformation-arteriovenous_malformation_1|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Capillary_malformation-arteriovenous_malformation_1|Parkes_Weber_syndrome|not_provided": 1,
    "Parkes_Weber_syndrome|not_provided|Capillary_malformation-arteriovenous_malformation_1": 1,
    "not_provided|Parkes_Weber_syndrome|Capillary_malformation-arteriovenous_malformation_1": 1,
    "TMEM161B-related_lissencephaly": 2,
    "Intellectual_Disability|_Stereotypic_Movements|_Epilepsy|_and/or_Cerebral_Malformations": 11,
    "Intellectual_Disability|_Stereotypic_Movements|_Epilepsy|_and/or_Cerebral_Malformations|not_provided": 5,
    "not_provided|Intellectual_Disability|_Stereotypic_Movements|_Epilepsy|_and/or_Cerebral_Malformations": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 317,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|Inborn_genetic_diseases": 4,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_provided": 11,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_specified|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 15,
    "Inborn_genetic_diseases|not_specified|not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 3,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 2,
    "Inborn_genetic_diseases|Syndromic_intellectual_disability|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "not_specified|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 9,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_specified": 3,
    "not_specified|Inborn_genetic_diseases|MEF2C-related_disorder|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "not_specified|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 6,
    "MEF2C-related_disorder|not_specified|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "MEF2C-related_disorder": 6,
    "not_specified|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "5q14.3_microdeletion_syndrome|Autism_spectrum_disorder|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|Intellectual_disability": 1,
    "MEF2C-related_disorder|not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "MEF2C-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 2,
    "Inborn_genetic_diseases|MEF2C-related_disorder|not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "MEF2C-related_complex_neurodevelopmental_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|Inborn_genetic_diseases": 1,
    "not_specified|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|MEF2C-related_disorder": 1,
    "not_provided|MEF2C-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_provided|MEF2C-related_disorder": 1,
    "intellectual_deficiency|Epilepsy": 2,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|MEF2C-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|Neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|Inborn_genetic_diseases|not_provided|Seizure": 1,
    "not_provided|Autism_spectrum_disorder|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language": 1,
    "MEF2C-related_disorder|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_provided": 1,
    "MEF2C_Haploinsufficiency_Syndrome": 1,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_stereotypic_hand_movements|_and_impaired_language|not_provided|Inborn_genetic_diseases": 1,
    "MEF2C-related_disorder|not_specified": 1,
    "Frontotemporal_dementia|not_specified|Intellectual_Disability|_Stereotypic_Movements|_Epilepsy|_and/or_Cerebral_Malformations": 1,
    "Usher_syndrome_type_2C": 118,
    "not_provided|Usher_syndrome_type_2C|not_specified": 29,
    "not_provided|Usher_syndrome_type_2C": 83,
    "Usher_syndrome_type_2C|not_specified": 3,
    "not_specified|ADGRV1-related_disorder": 1,
    "Febrile_seizures|_familial|_4|not_provided|not_specified": 1,
    "not_provided|not_specified|ADGRV1-related_disorder": 6,
    "Febrile_seizures|_familial|_4": 24,
    "Usher_syndrome_type_2C|not_provided": 41,
    "Usher_syndrome_type_2C|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Usher_syndrome_type_2C|Inborn_genetic_diseases": 2,
    "Usher_syndrome_type_2C|not_provided|not_specified": 14,
    "not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 13,
    "not_provided|Febrile_seizures|_familial|_4": 6,
    "not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified": 13,
    "ADGRV1-related_disorder|not_provided": 28,
    "Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_provided": 13,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2C": 7,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided": 12,
    "not_provided|ADGRV1-related_disorder|not_specified": 3,
    "not_provided|ADGRV1-related_disorder|Usher_syndrome_type_2C|not_specified": 2,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 16,
    "not_specified|not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 5,
    "ADGRV1-related_disorder|Inborn_genetic_diseases|Usher_syndrome_type_2C|not_provided": 1,
    "Usher_syndrome|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2C": 1,
    "ADGRV1-related_disorder": 25,
    "Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2C": 1,
    "not_provided|not_specified|Usher_syndrome_type_2C": 16,
    "Retinal_dystrophy|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_provided": 2,
    "ADGRV1-related_disorder|not_specified|not_provided": 5,
    "Febrile_seizures|_familial|_4|not_provided|Autosomal_recessive_sensorineural_hearing_loss|Usher_syndrome|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|not_provided|ADGRV1-related_disorder": 1,
    "not_specified|Febrile_seizures|_familial|_1|not_provided": 1,
    "not_provided|ADGRV1-related_disorder": 19,
    "Usher_syndrome_type_2|not_provided|Inborn_genetic_diseases": 1,
    "ADGRV1-related_disorder|Usher_syndrome_type_2C|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|ADGRV1-related_disorder": 1,
    "Ear_malformation|Hearing_impairment|Retinal_dystrophy|not_provided": 1,
    "not_provided|Usher_syndrome_type_2C|not_specified|ADGRV1-related_disorder": 1,
    "ADGRV1-related_disorder|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2C": 2,
    "Usher_syndrome_type_2C|not_specified|Febrile_seizures|_familial|_4|not_provided": 1,
    "Usher_syndrome_type_2C|not_specified|Febrile_seizures|_familial|_4|ADGRV1-related_disorder|Usher_syndrome_type_2|not_provided|Idiopathic_generalized_epilepsy": 1,
    "ADGRV1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_specified|ADGRV1-related_disorder|Usher_syndrome_type_2|Retinitis_pigmentosa|not_provided|Usher_syndrome_type_2C": 1,
    "not_specified|not_provided|Usher_syndrome_type_2C": 34,
    "ADGRV1-related_disorder|not_specified|not_provided|Usher_syndrome_type_2C": 5,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified|not_provided": 1,
    "ADGRV1-related_disorder|not_provided|not_specified": 6,
    "Usher_syndrome_type_2C|not_provided|ADGRV1-related_disorder|not_specified": 3,
    "not_provided|Usher_syndrome_type_2C|ADGRV1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided|not_specified": 3,
    "not_provided|Usher_syndrome_type_2C|Retinal_dystrophy": 1,
    "Usher_syndrome_type_2|not_specified|not_provided": 1,
    "not_specified|ADGRV1-related_disorder|not_provided": 4,
    "Rare_genetic_deafness|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided": 1,
    "ADGRV1-related_disorder|not_specified|not_provided|Febrile_seizures|_familial|_4": 1,
    "ADGRV1-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|Inborn_genetic_diseases": 1,
    "not_specified|Usher_syndrome_type_2C|not_provided|ADGRV1-related_disorder": 1,
    "not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 12,
    "not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|Hearing_impairment": 1,
    "Inborn_genetic_diseases|ADGRV1-related_disorder|not_provided": 1,
    "not_provided|Usher_syndrome_type_2|not_specified": 1,
    "not_specified|not_provided|ADGRV1-related_disorder": 4,
    "not_provided|Vascular_disorder": 1,
    "Usher_syndrome|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|Inborn_genetic_diseases|not_provided": 6,
    "ADGRV1-related_disorder|not_provided|not_specified|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|ADGRV1-related_disorder": 2,
    "ADGRV1-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|Intellectual_disability": 1,
    "not_provided|Hearing_impairment|not_specified": 3,
    "not_specified|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2C": 1,
    "Usher_syndrome|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|Retinal_dystrophy|ADGRV1-related_disorder|Usher_syndrome_type_2|Usher_syndrome|not_provided|not_specified": 1,
    "Usher_syndrome_type_2C|not_provided|Febrile_seizures|_familial|_4|ADGRV1-related_disorder|not_specified": 1,
    "Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified|not_provided": 3,
    "not_specified|Usher_syndrome_type_2|not_provided": 1,
    "ADGRV1-related_disorder|Usher_syndrome_type_2C|not_provided|Febrile_seizures|_familial|_4|not_specified|Abnormal_activity_of_mitochondrial_respiratory_chain": 1,
    "not_specified|Usher_syndrome_type_2C|not_provided": 13,
    "not_specified|not_provided|Usher_syndrome_type_2C|ADGRV1-related_disorder": 2,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Usher_syndrome_type_2C|not_specified|Febrile_seizures|_familial|_4": 3,
    "not_specified|not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|Retinal_dystrophy": 1,
    "Cerebral_arteriovenous_malformation|Arteriovenous_malformation|Hand_tremor|Tremor": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_2C": 2,
    "Usher_syndrome_type_2C|not_specified|not_provided|ADGRV1-related_disorder": 2,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_provided|ADGRV1-related_disorder|Inborn_genetic_diseases": 1,
    "ADGRV1-related_disorder|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified|not_provided": 1,
    "Usher_syndrome_type_2C|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "not_provided|ADGRV1-related_disorder|not_specified|Inborn_genetic_diseases": 2,
    "Usher_syndrome_type_2|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|not_provided|Febrile_seizures|_familial|_4|not_specified": 1,
    "not_specified|Hearing_impairment|not_provided": 2,
    "Retinal_dystrophy|Usher_syndrome_type_2C|not_provided": 4,
    "Inborn_genetic_diseases|Usher_syndrome_type_2C|not_provided": 3,
    "Febrile_seizures|_familial|_4|not_specified": 1,
    "not_provided|ADGRV1-related_disorder|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2C": 3,
    "Usher_syndrome|Usher_syndrome_type_2C|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 4,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|Inborn_genetic_diseases": 1,
    "Usher_syndrome|Inborn_genetic_diseases|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_provided|Rare_genetic_deafness": 1,
    "not_specified|ADGRV1-related_disorder|Usher_syndrome_type_2C|not_provided": 1,
    "not_specified|Usher_syndrome_type_2C|ADGRV1-related_disorder|not_provided": 2,
    "not_provided|Rare_genetic_deafness|Usher_syndrome_type_2C": 1,
    "not_provided|Rare_genetic_deafness|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Usher_syndrome_type_2C": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided": 1,
    "not_specified|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided": 3,
    "Usher_syndrome_type_2C|not_specified|not_provided|Febrile_seizures|_familial|_4": 1,
    "Febrile_seizures|_familial|_4|not_provided": 4,
    "not_specified|not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 1,
    "not_specified|Meniere_disease|not_provided|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|Inborn_genetic_diseases|not_specified|Retinal_dystrophy|not_provided": 1,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified|ADGRV1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|Hearing_impairment|not_provided|not_specified": 1,
    "not_specified|not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 2,
    "ADGRV1-related_disorder|not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 1,
    "not_provided|Inborn_genetic_diseases|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "not_provided|Usher_syndrome_type_2C|ADGRV1-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Febrile_seizures|_familial|_4": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 1,
    "ADGRV1-related_disorder|Craniosynostosis_syndrome|not_specified|not_provided|Usher_syndrome_type_2C": 2,
    "ADGRV1-related_disorder|not_specified|Usher_syndrome_type_2C|not_provided": 1,
    "Febrile_seizures|_familial|_4|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Febrile_seizures|_familial|_4|not_specified": 2,
    "not_specified|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|ADGRV1-related_disorder|Usher_syndrome_type_2|not_provided|Idiopathic_generalized_epilepsy": 1,
    "Febrile_seizures|_familial|_1|not_specified|not_provided|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|Usher_syndrome_type_2|not_provided": 1,
    "Usher_syndrome|not_provided|Febrile_seizures|_familial|_4": 1,
    "Usher_syndrome_type_2C|Rare_genetic_deafness|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "not_provided|Usher_syndrome|Inborn_genetic_diseases": 1,
    "ADGRV1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Usher_syndrome_type_2C|ADGRV1-related_disorder|not_provided|not_specified": 2,
    "Febrile_seizures|_familial|_4|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Usher_syndrome_type_2C|Usher_syndrome_type_2": 1,
    "not_specified|not_provided|ADGRV1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2C|not_provided|not_specified|ADGRV1-related_disorder": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2C": 2,
    "Usher_syndrome_type_2|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2C|not_provided|not_specified|Febrile_seizures|_familial|_4": 1,
    "not_provided|not_specified|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|Hearing_impairment": 1,
    "not_provided|Hearing_impairment|Usher_syndrome_type_2": 1,
    "not_provided|ADGRV1-related_disorder|Usher_syndrome": 1,
    "Usher_syndrome_type_2C|Inborn_genetic_diseases|Usher_syndrome_type_2|not_provided|ADGRV1-related_disorder|Febrile_seizures|_familial|_4": 1,
    "ADGRV1-related_disorder|Usher_syndrome_type_2C|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "ADGRV1-related_myoclonic_epilepsy": 1,
    "not_provided|not_specified|ADGRV1-related_disorder|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_provided|Rare_genetic_deafness": 2,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_provided|Usher_syndrome|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|Retinal_dystrophy": 1,
    "ADGRV1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Optic_atrophy|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "Retinal_dystrophy|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Usher_syndrome_type_2C|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Febrile_seizures|_familial|_1|Inborn_genetic_diseases": 1,
    "ADGRV1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2C|Usher_syndrome|not_provided|not_specified": 1,
    "Usher_syndrome_type_2C|Retinal_dystrophy|not_provided": 1,
    "not_provided|Usher_syndrome_type_2C|ADGRV1-related_disorder": 1,
    "Usher_syndrome_type_2C|ADGRV1-related_disorder": 1,
    "not_provided|Febrile_seizures|_familial|_4|not_specified|Idiopathic_generalized_epilepsy": 1,
    "Usher_syndrome_type_1": 349,
    "Inborn_genetic_diseases|not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified": 1,
    "not_provided|not_specified|Retinal_dystrophy|Rare_genetic_deafness": 1,
    "ADGRV1-related_disorder|not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|not_provided|not_specified|Usher_syndrome_type_2": 1,
    "Usher_syndrome_type_2C|Usher_syndrome_type_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hearing_impairment|not_provided": 2,
    "Usher_syndrome_type_2C|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified": 1,
    "Usher_syndrome_type_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|ADGRV1-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_provided": 1,
    "not_provided|ADGRV1-related_disorder|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2|Rare_genetic_deafness|Usher_syndrome_type_2C|not_provided|Febrile_seizures|_familial|_4|Usher_syndrome|Retinal_dystrophy": 1,
    "Optic_atrophy|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_2C|not_specified": 1,
    "ADGRV1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_2C": 1,
    "Retinal_dystrophy|not_provided|Febrile_seizures|_familial|_4": 1,
    "not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified|ADGRV1-related_disorder": 1,
    "ADGRV1-related_disorder|Retinal_dystrophy|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_2C": 1,
    "Usher_syndrome_type_2C|Meniere_disease|not_provided|not_specified": 1,
    "not_provided|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_specified": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_2C|not_specified|not_provided": 1,
    "Febrile_seizures|_familial|_4|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2|not_provided|Usher_syndrome_type_2C": 1,
    "Usher_syndrome|_type_IIC|_GPR98/PDZD7_digenic": 2,
    "Usher_syndrome_type_2C|not_provided|Febrile_seizures|_familial|_4": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|ADGRV1-related_disorder": 1,
    "not_provided|Usher_syndrome_type_2|not_specified|Inborn_genetic_diseases": 1,
    "Usher_syndrome|Febrile_seizures|_familial|_4|Usher_syndrome_type_2C|not_provided": 1,
    "ADGRV1-related_disorder|Inborn_genetic_diseases|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified|not_provided": 1,
    "Usher_syndrome_type_2C|not_specified|ADGRV1-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_2C|Febrile_seizures|_familial|_4": 1,
    "Usher_syndrome_type_2C|Febrile_seizures|_familial|_4|not_specified|not_provided|ADGRV1-related_disorder|Inborn_genetic_diseases": 1,
    "Bosch-Boonstra-Schaaf_optic_atrophy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Bosch-Boonstra-Schaaf_optic_atrophy_syndrome": 67,
    "Bosch-Boonstra-Schaaf_optic_atrophy_syndrome|not_provided": 11,
    "not_provided|Inborn_genetic_diseases|NR2F1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|NR2F1-related_disorder": 1,
    "Bosch-Boonstra-Schaaf_optic_atrophy_syndrome|Epilepsy": 1,
    "NR2F1-related_disorder": 4,
    "not_provided|Bosch-Boonstra-Schaaf_optic_atrophy_syndrome": 3,
    "Inborn_genetic_diseases|Bosch-Boonstra-Schaaf_optic_atrophy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Bosch-Boonstra-Schaaf_optic_atrophy_syndrome": 1,
    "not_provided|NR2F1-related_disorder": 3,
    "NR2F1-related_disorder|not_provided": 1,
    "KIAA0825-related_disorder": 19,
    "Polydactyly|_postaxial|_type_a10": 8,
    "not_provided|Polydactyly|_postaxial|_type_a10": 1,
    "Polydactyly|_postaxial|_type_a10|KIAA0825-related_disorder": 2,
    "KIAA0825-related_disorder|not_specified": 1,
    "Polydactyly|_postaxial|_type_A1|Autosomal_recessive_nonsyndromic_postaxial_polydactyly|not_provided|Polydactyly|_postaxial|_type_a10": 1,
    "not_provided|KIAA0825-related_disorder": 1,
    "not_specified|KIAA0825-related_disorder": 3,
    "Polydactyly|_postaxial|_type_A1|Autosomal_recessive_nonsyndromic_postaxial_polydactyly|Polydactyly|_postaxial|_type_a10": 1,
    "Trichohepatoenteric_syndrome_1": 23,
    "SKIC3-related_disorder|not_provided": 12,
    "not_provided|SKIC3-related_disorder": 11,
    "Trichohepatoenteric_syndrome_1|not_provided|not_specified": 2,
    "not_specified|not_provided|Trichohepatoenteric_syndrome_1": 1,
    "not_provided|Trichohepatoenteric_syndrome_1|Inborn_genetic_diseases": 2,
    "not_provided|Trichohepatoenteric_syndrome_1": 20,
    "Trichohepatoenteric_syndrome_1|not_provided|Trichohepatoenteric_syndrome": 2,
    "not_provided|Trichohepatoenteric_syndrome_1|SKIC3-related_disorder": 3,
    "Trichohepatoenteric_syndrome_1|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Trichohepatoenteric_syndrome_1": 1,
    "not_specified|SKIC3-related_disorder|not_provided": 1,
    "SKIC3-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "SKIC3-related_disorder|not_provided|Trichohepatoenteric_syndrome_1": 2,
    "Trichohepatoenteric_syndrome|not_provided": 6,
    "not_provided|Trichohepatoenteric_syndrome": 4,
    "Inherited_Immunodeficiency_Diseases|Trichohepatoenteric_syndrome_1|not_provided": 1,
    "SKIC3-related_disorder|not_provided|not_specified": 1,
    "SKIC3-related_disorder": 3,
    "SKIC3-related_disorder|Trichohepatoenteric_syndrome_1|not_provided": 1,
    "Trichohepatoenteric_syndrome": 15,
    "Trichohepatoenteric_syndrome_1|Inborn_genetic_diseases|SKIC3-related_disorder|not_provided": 1,
    "Trichohepatoenteric_syndrome_1|Trichohepatoenteric_syndrome": 1,
    "Inherited_Immunodeficiency_Diseases|Trichohepatoenteric_syndrome_1": 1,
    "Trichohepatoenteric_syndrome_1|not_specified|not_provided": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|SKIC3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Trichohepatoenteric_syndrome": 1,
    "Mucopolysaccharidosis|_type_10": 5,
    "ARSK-related_disorder": 3,
    "Obesity_due_to_prohormone_convertase_I_deficiency": 45,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency": 23,
    "Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_prohormone_convertase_I_deficiency": 2,
    "Obesity_due_to_prohormone_convertase_I_deficiency|Monogenic_Non-Syndromic_Obesity": 8,
    "not_provided|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency": 1,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency|not_provided": 8,
    "PCSK1-related_disorder": 148,
    "not_provided|PCSK1-related_disorder": 17,
    "not_provided|Obesity_due_to_prohormone_convertase_I_deficiency|Inborn_genetic_diseases|PCSK1-related_disorder": 1,
    "Inborn_genetic_diseases|PCSK1-related_disorder": 8,
    "PCSK1-related_disorder|Monogenic_Non-Syndromic_Obesity|Body_mass_index_quantitative_trait_locus_12|Obesity_due_to_prohormone_convertase_I_deficiency": 1,
    "not_specified|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency|not_provided": 3,
    "PCSK1-related_disorder|not_specified|not_provided|Obesity_due_to_prohormone_convertase_I_deficiency": 1,
    "PCSK1-related_disorder|not_provided": 9,
    "not_specified|PCSK1-related_disorder|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency|not_provided": 3,
    "PCSK1-related_disorder|not_specified|not_provided": 3,
    "PCSK1-related_disorder|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency": 1,
    "PCSK1-related_disorder|Obesity_due_to_prohormone_convertase_I_deficiency|Body_mass_index_quantitative_trait_locus_12": 1,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_prohormone_convertase_I_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|PCSK1-related_disorder|Obesity_due_to_prohormone_convertase_I_deficiency": 2,
    "not_provided|Body_mass_index_quantitative_trait_locus_12|Obesity_due_to_prohormone_convertase_I_deficiency": 2,
    "Body_mass_index_quantitative_trait_locus_12|Obesity_due_to_prohormone_convertase_I_deficiency|PCSK1-related_disorder": 1,
    "PCSK1-related_disorder|Obesity_due_to_prohormone_convertase_I_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Obesity_due_to_prohormone_convertase_I_deficiency": 2,
    "PCSK1-related_disorder|Inborn_genetic_diseases": 1,
    "Obesity_due_to_prohormone_convertase_I_deficiency|not_provided": 4,
    "Obesity_due_to_prohormone_convertase_I_deficiency|not_provided|PCSK1-related_disorder": 3,
    "not_provided|PCSK1-related_disorder|Inborn_genetic_diseases": 1,
    "Obesity_due_to_prohormone_convertase_I_deficiency|PCSK1-related_disorder": 2,
    "not_specified|Obesity_due_to_prohormone_convertase_I_deficiency|not_provided|PCSK1-related_disorder": 1,
    "not_provided|Body_mass_index_quantitative_trait_locus_12|not_specified": 1,
    "Obesity_due_to_prohormone_convertase_I_deficiency|Body_mass_index_quantitative_trait_locus_12": 1,
    "Inborn_genetic_diseases|PCSK1-related_disorder|Obesity_due_to_prohormone_convertase_I_deficiency": 1,
    "Obesity_due_to_prohormone_convertase_I_deficiency|not_provided|Body_mass_index_quantitative_trait_locus_12|PCSK1-related_disorder": 1,
    "PCSK1-related_disorder|not_specified": 1,
    "Body_mass_index_quantitative_trait_locus_12|Obesity_due_to_prohormone_convertase_I_deficiency|not_provided|PCSK1-related_disorder": 1,
    "Obesity_due_to_prohormone_convertase_I_deficiency|Inborn_genetic_diseases|PCSK1-related_disorder": 1,
    "Peeling_skin-leukonuchia-acral_punctate_keratoses-cheilitis-knuckle_pads_syndrome": 11,
    "not_provided|Peeling_skin-leukonuchia-acral_punctate_keratoses-cheilitis-knuckle_pads_syndrome": 4,
    "CAST-related_disorder": 8,
    "CAST-related_disorder|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|CAST-related_disorder": 2,
    "not_provided|CAST-related_disorder": 5,
    "Peeling_skin-leukonuchia-acral_punctate_keratoses-cheilitis-knuckle_pads_syndrome|not_provided": 1,
    "ERAP1-related_disorder|not_provided": 1,
    "Pilarowski-Bjornsson_syndrome|not_provided": 4,
    "Neurodevelopmental_disorder_with_microcephaly|_epilepsy|_and_brain_atrophy": 8,
    "Pilarowski-Bjornsson_syndrome": 65,
    "not_provided|CHD1-related_disorder": 6,
    "not_specified|Pilarowski-Bjornsson_syndrome": 4,
    "CHD1-related_disorder|not_provided": 2,
    "CHD1-related_disorder": 15,
    "not_provided|CHD1-related_disorder|Complex_neurodevelopmental_disorder": 1,
    "not_specified|CHD1-related_disorder": 1,
    "CHD1-related_disorder|not_specified": 2,
    "not_provided|Pilarowski-Bjornsson_syndrome": 5,
    "not_specified|not_provided|Pilarowski-Bjornsson_syndrome": 1,
    "Pilarowski-Bjornsson_syndrome|not_specified": 2,
    "Mitochondrial_DNA_depletion_syndrome_13": 251,
    "Thyroid_cancer|_nonmedullary|_4|Bamforth-Lazarus_syndrome": 2,
    "PPIP5K2-related_disorder": 7,
    "Hearing_loss|_autosomal_recessive_100": 1,
    "not_provided|PPIP5K2-related_disorder": 3,
    "not_provided|Hearing_loss|_autosomal_recessive_100": 1,
    "not_specified|PPIP5K2-related_disorder": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B": 237,
    "SLC25A46-related_disorder": 3,
    "not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6B|Pontocerebellar_hypoplasia|_type_1E|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 20,
    "Pontocerebellar_hypoplasia|_type_1E": 5,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_provided": 3,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Inborn_genetic_diseases": 10,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_provided": 12,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_specified|Pontocerebellar_hypoplasia|_type_1E|Inborn_genetic_diseases|not_provided": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_specified|not_provided": 1,
    "not_provided|SLC25A46-related_disorder|Neuropathy|_hereditary_motor_and_sensory|_type_6B|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_specified": 2,
    "SLC25A46-related_disorder|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 1,
    "not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 5,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 2,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_specified|SLC25A46-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 1,
    "Optic_atrophy|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 1,
    "SLC25A46-associated_optic_atrophy_spectrum_disorder": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Inborn_genetic_diseases|SLC25A46-related_disorder|not_provided": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|SLC25A46-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Pontocerebellar_hypoplasia|_type_1E|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 4,
    "not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6B|Optic_atrophy|not_specified": 1,
    "not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6B|not_specified|SLC25A46-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Pontocerebellar_hypoplasia|_type_1E": 2,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Inborn_genetic_diseases|not_provided|SLC25A46-related_disorder": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_motor_and_sensory|_type_6B|SLC25A46-related_disorder|not_provided": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Inborn_genetic_diseases|not_provided": 1,
    "Pontocerebellar_hypoplasia|_type_1E|not_provided": 1,
    "not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_6B|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_motor_and_sensory|_type_6B|Spastic_ataxia|SLC25A46-related_disorder": 1,
    "Neuropathy|_hereditary_motor_and_sensory|_type_6B|Charcot-Marie-Tooth_disease": 1,
    "SLC25A46-associated_optic_atrophy_spectrum_disorder|Neuropathy|_hereditary_motor_and_sensory|_type_6B": 1,
    "not_provided|Pontocerebellar_hypoplasia|_type_1E": 1,
    "not_provided|Primary_open_angle_glaucoma|not_specified": 1,
    "Glaucoma_1|_open_angle|_G": 2,
    "High_myopia|not_provided|not_specified|Glaucoma_1|_open_angle|_G": 1,
    "not_provided|Primary_open_angle_glaucoma|WDR36-related_disorder": 1,
    "not_provided|WDR36-related_disorder": 3,
    "WDR36-related_disorder": 3,
    "WDR36-related_disorder|not_provided": 2,
    "not_provided|Glaucoma_1|_open_angle|_G": 3,
    "Glaucoma_1|_open_angle|_G|not_specified": 3,
    "Glaucoma_1|_open_angle|_G|not_provided|not_specified": 1,
    "not_provided|Usher_syndrome_type_2C|Glaucoma_1|_open_angle|_G|WDR36-related_disorder": 1,
    "not_specified|Glaucoma_1|_open_angle|_G|not_provided": 2,
    "not_provided|Primary_open_angle_glaucoma": 4,
    "not_specified|WDR36-related_disorder": 1,
    "Glaucoma_1|_open_angle|_G|not_provided": 2,
    "Primary_open_angle_glaucoma": 18,
    "not_specified|not_provided|Glaucoma_1|_open_angle|_G": 1,
    "Intellectual_disability|Involuntary_movements|not_provided": 1,
    "Failure_to_thrive|Spastic_paraplegia": 1,
    "Familial_adenomatous_polyposis_1": 4969,
    "Familial_adenomatous_polyposis_1|APC-related_disorder": 14,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified": 4,
    "not_specified|Familial_adenomatous_polyposis_1": 42,
    "Familial_adenomatous_polyposis_1|Attenuated_familial_adenomatous_polyposis|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach": 1,
    "Familial_adenomatous_polyposis_1|not_specified": 30,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1": 5,
    "not_provided|Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified": 2,
    "Desmoid_disease|_hereditary|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1687,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 49,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1600,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 48,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Periampullary_adenoma|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 121,
    "Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|not_specified": 7,
    "not_provided|Familial_adenomatous_polyposis_1|not_specified": 6,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer": 2,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified": 1,
    "not_provided|Familial_adenomatous_polyposis_1": 113,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer": 1,
    "Familial_adenomatous_polyposis_1|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_1|not_provided": 111,
    "Desmoid_disease|_hereditary|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|not_provided|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 164,
    "not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 7,
    "Classic_or_attenuated_familial_adenomatous_polyposis": 104,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 16,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 69,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 49,
    "Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach": 1,
    "Colorectal_cancer|Gastric_cancer|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma": 2,
    "Hepatocellular_carcinoma|Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer": 1,
    "Desmoid_disease|_hereditary|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|not_provided": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided|not_specified": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1": 6,
    "APC-related_disorder|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_cancer|Colorectal_cancer|not_specified": 1,
    "Familial_adenomatous_polyposis_1|not_provided|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder": 49,
    "APC-related_disorder|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "not_specified|Familial_adenomatous_polyposis_1|APC-related_disorder": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 41,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 56,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1": 2,
    "not_specified|APC-related_disorder|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "APC-related_disorder|not_provided|Familial_adenomatous_polyposis_1": 1,
    "not_provided|APC-related_disorder": 1,
    "APC-related_disorder|not_specified|not_provided": 1,
    "not_provided|APC-related_disorder|not_specified": 1,
    "not_provided|Familial_colorectal_cancer": 3,
    "Familial_colorectal_cancer|not_provided": 16,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Carcinoma_of_colon": 1,
    "Desmoid_tumor|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 29,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 13,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 16,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 22,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 33,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 7,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 51,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 88,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 96,
    "not_provided|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 4,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Attenuated_familial_adenomatous_polyposis|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1": 16,
    "APC-Associated_Polyposis_Disorders": 40,
    "Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|Desmoid_disease|_hereditary|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 7,
    "not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 21,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|not_provided|Neoplasm_of_stomach": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 62,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 98,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 4,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 109,
    "not_specified|not_provided|Familial_colorectal_cancer|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "Gastric_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 77,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 99,
    "Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 87,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 3,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 14,
    "not_specified|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Carcinoma_of_colon|Familial_adenomatous_polyposis_1": 7,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 2,
    "not_specified|Familial_adenomatous_polyposis_1|not_provided": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 21,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 2,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Desmoid_disease|_hereditary|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 24,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "Desmoid_disease|_hereditary|Gastric_cancer|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Hepatocellular_carcinoma|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 3,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Turcot_syndrome_with_polyposis|Gardner_syndrome|Familial_adenomatous_polyposis_1|not_specified": 1,
    "APC-related_disorder|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_specified": 1,
    "APC-related_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 3,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 3,
    "Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_multiple_polyposis_syndrome|not_provided": 3,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to": 1,
    "not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 3,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 14,
    "Familial_colorectal_cancer|Familial_adenomatous_polyposis_1": 4,
    "Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 110,
    "Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 16,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 2,
    "Desmoid_disease|_hereditary|Colorectal_cancer|Familial_adenomatous_polyposis_1|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 6,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 8,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 17,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-Associated_Polyposis_Disorders|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Breast_carcinoma": 1,
    "Hepatocellular_carcinoma|Gastric_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer": 1,
    "Familial_adenomatous_polyposis_1|Colorectal_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided": 3,
    "APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hepatocellular_carcinoma|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified": 26,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 13,
    "Desmoid_disease|_hereditary|Gastric_cancer|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "APC-related_disorder|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_provided|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Gastric_cancer|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Hepatocellular_carcinoma": 2,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 5,
    "Familial_adenomatous_polyposis_1|not_provided|Carcinoma_of_colon": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 15,
    "Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 13,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified|Colorectal_adenoma|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|APC-Associated_Polyposis_Disorders|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|not_provided": 2,
    "not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 7,
    "Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome": 14,
    "Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 4,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 3,
    "Familial_multiple_polyposis_syndrome": 25,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 19,
    "Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|Carcinoma_of_colon": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 3,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 7,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "not_provided|Colorectal_cancer|_susceptibility_to|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 6,
    "Colorectal_cancer|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Hepatocellular_carcinoma|APC-related_disorder|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 5,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 17,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_multiple_polyposis_syndrome|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Desmoid_disease|_hereditary|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 9,
    "Gardner_syndrome|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Neoplasm_of_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 8,
    "Colorectal_cancer|Gastric_cancer|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRAIN_TUMOR-POLYPOSIS_SYNDROME_2": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 4,
    "Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_cancer|Colorectal_cancer|Carcinoma_of_colon|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Hereditary_cancer|APC-Associated_Polyposis_Disorders|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 4,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-related_disorder": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 5,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 7,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 4,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Colon_cancer|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "not_provided|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 6,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_disorder": 6,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Carcinoma_of_colon|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 25,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Rectum_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "not_provided|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon": 1,
    "not_provided|not_specified|Familial_adenomatous_polyposis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 2,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 4,
    "Gardner_syndrome|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1": 7,
    "Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Carcinoma_of_colon|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_provided|not_specified|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Gardner_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome": 6,
    "Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Neoplasm_of_stomach|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Gastrointestinal_stromal_tumor": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Ovarian_cancer": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 3,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 12,
    "Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided|Familial_adenomatous_polyposis_1|Colorectal_cancer|_susceptibility_to|Gardner_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Gardner_syndrome|APC-related_attenuated_familial_adenomatous_polyposis|not_specified|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Carcinoma_of_colon|Desmoid_disease|_hereditary|Neoplasm_of_stomach": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|APC-related_disorder": 2,
    "not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_multiple_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 3,
    "Desmoid_disease|_hereditary": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|not_provided|Familial_adenomatous_polyposis_1|APC-related_disorder": 1,
    "Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Gastric_cancer": 1,
    "not_provided|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|not_specified|APC-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1": 5,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 20,
    "Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hepatocellular_carcinoma|Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 18,
    "Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Gardner_syndrome": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Familial_multiple_polyposis_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Colorectal_cancer|Desmoid_disease|_hereditary": 1,
    "not_provided|Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 6,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 6,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Neoplasm_of_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|not_provided": 3,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Colorectal_cancer|Familial_adenomatous_polyposis_1|Gastric_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 9,
    "Carcinoma_of_colon|Colonic_neoplasm|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1": 2,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma": 1,
    "Familial_colorectal_cancer|Familial_adenomatous_polyposis_1|not_specified": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided": 5,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 2,
    "Gastric_cancer|Familial_adenomatous_polyposis_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-Associated_Polyposis_Disorders|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_colorectal_cancer": 1,
    "Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Familial_adenomatous_polyposis_1|Colon_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|APC-Associated_Polyposis_Disorders|APC-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "APC-Associated_Polyposis_Disorders|Carcinoma_of_colon|Gardner_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "not_specified|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|not_provided": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 3,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_cancer|Colorectal_cancer|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer": 4,
    "not_provided|Familial_adenomatous_polyposis_1|not_specified|Hepatocellular_carcinoma|Carcinoma_of_colon|Neoplasm_of_stomach|Desmoid_disease|_hereditary|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders": 2,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Neoplasm_of_the_liver": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Hereditary_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_cancer": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|BRAIN_TUMOR-POLYPOSIS_SYNDROME_2": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_cancer|Colorectal_cancer": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 2,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "not_specified|Desmoid_disease|_hereditary|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Familial_colorectal_cancer": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Neoplasm_of_stomach|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided|Colorectal_cancer|_susceptibility_to": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Familial_multiple_polyposis_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|not_specified|Familial_adenomatous_polyposis_1": 1,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 3,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|APC-related_disorder": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 7,
    "Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "not_provided|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colon_cancer|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 4,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "not_provided|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer": 1,
    "Carcinoma_of_colon|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 1,
    "not_provided|Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 2,
    "Familial_adenomatous_polyposis_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|Familial_colorectal_cancer|not_provided|Familial_adenomatous_polyposis_1|not_specified|Carcinoma_of_colon": 1,
    "APC-Associated_Polyposis_Disorders|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 4,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Familial_adenomatous_polyposis_1|not_provided|Rectum_adenocarcinoma|Duodenal_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 9,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 3,
    "Familial_adenomatous_polyposis_1|Gardner_syndrome": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 13,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 4,
    "Gardner_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Monoclonal_B-Cell_Lymphocytosis": 1,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Colorectal_cancer|_susceptibility_to|Neoplasm_of_the_liver|not_provided|Hereditary_cancer|not_specified": 1,
    "not_specified|Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|not_specified|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Desmoid_disease|_hereditary": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_provided": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 2,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Familial_colorectal_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|APC-related_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Neoplasm_of_the_liver|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Desmoid_disease|_hereditary|Gastric_cancer|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_provided|APC-Associated_Polyposis_Disorders|not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "Familial_adenomatous_polyposis_1|not_provided|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Turcot_syndrome_with_polyposis": 1,
    "APC-related_disorder|not_provided": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 2,
    "not_provided|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_adenomatous_polyposis_1": 1,
    "not_specified|Familial_multiple_polyposis_syndrome|APC-related_disorder|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 3,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|APC-related_disorder|APC-Associated_Polyposis_Disorders": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Duodenal_adenocarcinoma": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_cancer|Colorectal_cancer|Desmoid_disease|_hereditary|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Gardner_syndrome|APC-related_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer|not_provided|Familial_multiple_polyposis_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1": 2,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|not_specified|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_multiple_polyposis_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 4,
    "not_provided|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 3,
    "Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 4,
    "Familial_adenomatous_polyposis_1|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Neoplasm_of_the_liver": 1,
    "Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|not_provided|Familial_multiple_polyposis_syndrome|Colorectal_cancer|_susceptibility_to": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Desmoid_disease|_hereditary": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_multiple_polyposis_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_provided|not_specified|APC-related_disorder|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Colon_cancer": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_adenomatous_polyposis_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "APC-related_disorder|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rectum_adenocarcinoma": 1,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Craniopharyngioma|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_multiple_polyposis_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 2,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 2,
    "Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Colorectal_cancer|Gastric_cancer|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Endometrial_carcinoma": 1,
    "APC-Associated_Polyposis_Disorders|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|Familial_adenomatous_polyposis_1": 1,
    "Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|APC-Associated_Polyposis_Disorders|not_specified|not_provided|Neoplasm_of_the_liver|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Ovarian_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_multiple_polyposis_syndrome|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_adenomatous_polyposis_1|Familial_colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_specified|not_provided|Desmoid_disease|_hereditary|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_multiple_polyposis_syndrome|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hepatocellular_carcinoma|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1": 6,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Colorectal_cancer|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach": 1,
    "Familial_multiple_polyposis_syndrome|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "APC-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Carcinoma_of_colon": 1,
    "Hereditary_cancer|APC-related_disorder|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hepatocellular_carcinoma|Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Colon_cancer|Neoplasm_of_the_liver": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Familial_adenomatous_polyposis_1|not_provided|not_specified": 1,
    "Hepatoblastoma|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Carcinoma_of_colon|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_provided|not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Carcinoma_of_colon|not_provided|Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|Familial_multiple_polyposis_syndrome|not_provided|Familial_adenomatous_polyposis_1|Familial_colorectal_cancer|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|.|Breast_cancer|_susceptibility_to|Breast_carcinoma": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_cancer|Desmoid_disease|_hereditary|APC-related_disorder|Duodenal_polyposis|Hyperplastic_colonic_polyposis|Gastric_polyposis|Adenomatous_colonic_polyposis|Intestinal_polyp|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Colon_adenocarcinoma|Carcinoma_of_colon|Gardner_syndrome|ADENOMATOUS_POLYPOSIS_COLI_WITH_CONGENITAL_CHOLESTEATOMA": 1,
    "not_provided|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|not_specified": 1,
    "not_provided|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Gastric_cancer|Colorectal_cancer|APC-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Ovarian_cancer": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Colorectal_cancer|_susceptibility_to|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 3,
    "Desmoid_disease|_hereditary|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Colorectal_cancer|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hepatocellular_carcinoma|Gastric_cancer|Desmoid_disease|_hereditary|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Desmoid_disease|_hereditary|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Neoplasm_of_the_liver": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "not_provided|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 3,
    "Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_multiple_polyposis_syndrome|APC-Associated_Polyposis_Disorders|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Familial_multiple_polyposis_syndrome|not_specified|APC-Associated_Polyposis_Disorders|Colorectal_adenoma|not_provided|Familial_colorectal_cancer": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Neoplasm_of_stomach|Desmoid_disease|_hereditary|Carcinoma_of_colon|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|Periampullary_adenoma|Gardner_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Periampullary_adenoma": 1,
    "Familial_adenomatous_polyposis_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Intrahepatic_cholangiocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Desmoid_tumor": 1,
    "APC-Associated_Polyposis_Disorders|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_colorectal_cancer|Carcinoma_of_colon": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|not_specified|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Familial_adenomatous_polyposis_1": 1,
    "not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Familial_adenomatous_polyposis_1|Gastrointestinal_stromal_tumor_of_small_intestine|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|not_provided|APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Colorectal_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_multiple_polyposis_syndrome|Gardner_syndrome": 1,
    "Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Atypical_endometrial_hyperplasia|not_provided": 1,
    "not_provided|Familial_multiple_polyposis_syndrome": 2,
    "Klatskin_tumor|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Malignant_tumor_of_pancreas|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Colorectal_cancer|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Neoplasm_of_the_liver": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Colorectal_adenoma": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer|APC-Associated_Polyposis_Disorders|Gastric_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided": 3,
    "Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|not_provided|Carcinoma_of_colon|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Adenomatous_colonic_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gardner_syndrome|APC-related_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_specified|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_cancer": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 3,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|not_provided|Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer|Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided|Colon_cancer": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Familial_colorectal_cancer": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 2,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Neoplasm_of_stomach|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_adenomatous_polyposis_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Carcinoma_of_colon|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1|not_provided|not_specified": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders|not_specified|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1": 2,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|not_specified": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hepatocellular_carcinoma|Gastric_cancer|Desmoid_disease|_hereditary|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 3,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_specified|Desmoid_disease|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders": 1,
    "not_provided|Familial_adenomatous_polyposis_1|APC-related_attenuated_familial_adenomatous_polyposis|Gardner_syndrome|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Familial_colorectal_cancer": 1,
    "Familial_adenomatous_polyposis_1|Gastrointestinal_stromal_tumor_of_small_intestine": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|not_provided|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-Associated_Polyposis_Disorders|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|APC-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|APC-related_disorder|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_multiple_polyposis_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Ovarian_cancer|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hepatocellular_carcinoma|Gastric_cancer|APC-related_disorder|APC-Associated_Polyposis_Disorders|Neoplasm_of_stomach|Carcinoma_of_colon|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Colorectal_cancer|_susceptibility_to": 1,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|Gastric_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|APC-Associated_Polyposis_Disorders": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_specified|APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Carcinoma_of_colon|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|not_specified|Familial_adenomatous_polyposis_1": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided|APC-Associated_Polyposis_Disorders": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Familial_adenomatous_polyposis_1": 2,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_glioma|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Rectum_adenocarcinoma|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 2,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Carcinoma_of_colon|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_provided|not_specified": 1,
    "Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Malignant_tumor_of_breast": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "not_provided|not_specified|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|not_specified|not_provided|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 2,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cancer_or_benign_tumor|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-related_disorder": 2,
    "Malignant_tumor_of_ascending_colon|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 2,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Malignant_tumor_of_breast": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1": 2,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 2,
    "Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Carcinoma_of_colon|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_specified|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Colorectal_cancer|_susceptibility_to|APC-related_disorder|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Desmoid_disease|_hereditary": 1,
    "Familial_multiple_polyposis_syndrome|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Carcinoma_of_colon|Hepatocellular_carcinoma|APC-related_disorder|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Familial_multiple_polyposis_syndrome|not_specified": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_multiple_polyposis_syndrome|Carcinoma_of_colon": 1,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Familial_colorectal_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|APC-related_disorder|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|APC-Associated_Polyposis_Disorders|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_adenomatous_polyposis_1|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|APC-related_attenuated_familial_adenomatous_polyposis|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "APC-related_disorder|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Sigmoid_colon_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Neoplasm_of_stomach": 1,
    "APC-Associated_Polyposis_Disorders|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Neoplasm_of_stomach|Hepatocellular_carcinoma|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|not_provided": 2,
    "not_specified|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|Familial_adenomatous_polyposis_1": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Desmoid_disease|_hereditary|Neoplasm_of_stomach|Carcinoma_of_colon|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Carcinoma_of_colon|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Colorectal_cancer|_susceptibility_to": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|Malignant_tumor_of_breast|not_specified|Familial_adenomatous_polyposis_1": 1,
    "APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified|Familial_adenomatous_polyposis_1": 2,
    "APC-related_disorder|Hereditary_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "not_specified|APC-related_disorder|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-Associated_Polyposis_Disorders|not_specified|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neoplasm_of_stomach|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_specified|Carcinoma_of_colon|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "APC-related_disorder|Familial_adenomatous_polyposis_1|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|Hereditary_cancer|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_multiple_polyposis_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Desmoid_disease|_hereditary|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "APC-related_disorder|not_specified|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-related_disorder|Hereditary_cancer": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|Desmoid_disease|_hereditary|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_multiple_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified|not_provided": 1,
    "not_provided|not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_specified|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Familial_adenomatous_polyposis_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|not_specified": 1,
    "not_provided|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_cancer|Hepatocellular_carcinoma": 1,
    "not_provided|Colorectal_cancer|Colorectal_adenoma|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|APC-related_disorder|not_specified|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 2,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Colon_adenocarcinoma|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_1": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder": 1,
    "Hepatocellular_carcinoma|Gastric_cancer|Desmoid_disease|_hereditary|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-related_disorder": 1,
    "Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Colorectal_cancer|Gastric_cancer|Hepatocellular_carcinoma": 1,
    "not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|not_specified|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1": 2,
    "not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Gastric_cancer|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|APC-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma|Colorectal_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Gastric_cancer|Desmoid_disease|_hereditary|Familial_adenomatous_polyposis_1|Hepatocellular_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer|Familial_adenomatous_polyposis_1": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "APC-Associated_Polyposis_Disorders|Hereditary_cancer-predisposing_syndrome|Colorectal_adenoma|Ovarian_cancer|not_specified|not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis|not_specified": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Neoplasm_of_stomach|Desmoid_disease|_hereditary|Carcinoma_of_colon|Hepatocellular_carcinoma|not_provided|not_specified": 1,
    "not_specified|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Hepatocellular_carcinoma|Gastric_cancer|Colorectal_cancer|Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided|APC-related_disorder": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "APC-related_disorder|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1": 1,
    "Intrahepatic_cholangiocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hepatocellular_carcinoma|Familial_adenomatous_polyposis_1|Desmoid_disease|_hereditary|APC-related_disorder|Neoplasm_of_the_liver": 1,
    "Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|APC-related_disorder|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Colorectal_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_1|not_specified|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|Desmoid_disease|_hereditary|not_provided|Hepatocellular_carcinoma|Neoplasm_of_stomach|Carcinoma_of_colon": 1,
    "Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Desmoid_disease|_hereditary|Hepatocellular_carcinoma|Gastric_cancer|Familial_adenomatous_polyposis_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Neoplasm_of_the_liver|not_provided|Classic_or_attenuated_familial_adenomatous_polyposis": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Gastric_adenocarcinoma_and_proximal_polyposis_of_the_stomach|Attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|APC-Associated_Polyposis_Disorders|Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Classic_or_attenuated_familial_adenomatous_polyposis|Intrahepatic_cholangiocarcinoma": 1,
    "not_specified|Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|not_provided|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|Carcinoma_of_colon|Hepatocellular_carcinoma|Neoplasm_of_stomach": 1,
    "Familial_adenomatous_polyposis_1|Classic_or_attenuated_familial_adenomatous_polyposis|APC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Classic_or_attenuated_familial_adenomatous_polyposis|Familial_adenomatous_polyposis_1|APC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_1|not_provided|APC-related_disorder": 1,
    "Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|Desmoid_disease|_hereditary|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|Familial_adenomatous_polyposis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer|not_provided": 1,
    "APC-Associated_Polyposis_Disorders|not_provided": 3,
    "APC-Associated_Polyposis_Disorders|Familial_colorectal_cancer": 6,
    "Shwachman-Diamond_syndrome_1|Severe_congenital_neutropenia": 2,
    "YTHDC2-related_disorder": 38,
    "not_provided|YTHDC2-related_disorder": 5,
    "YTHDC2-related_disorder|not_specified": 3,
    "YTHDC2-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities": 20,
    "Dystonia_34|_myoclonic": 3,
    "Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities|Dystonia_34|_myoclonic": 3,
    "KCNN2-related_disorder": 2,
    "Dystonia_34|_myoclonic|Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities": 1,
    "KCNN2-related_disorder|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities|Motor_tics|Intellectual_disability|_severe|Autistic_behavior|Global_developmental_delay": 1,
    "KCNN2-related_Neurodevelopmental_movement_disorder": 1,
    "Cerebellar_ataxia|Intellectual_disability|_mild|Global_developmental_delay": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities|Motor_tics|Autistic_behavior|Global_developmental_delay|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Global_developmental_delay|KCNN2-related_disorder|Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities": 1,
    "Intellectual_disability|Global_developmental_delay|Bradykinesia|Motor_tics|not_specified": 1,
    "Cerebellar_ataxia|Intellectual_disability|Autistic_behavior|Global_developmental_delay|Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities": 1,
    "Autistic_behavior|Global_developmental_delay|Intellectual_disability|_mild|Seizure|not_provided": 1,
    "Dystonia_34|_myoclonic|not_provided": 1,
    "Intellectual_disability|_moderate|Global_developmental_delay|Autistic_behavior": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities|Autistic_behavior|Intellectual_disability|_moderate|Global_developmental_delay|Seizure": 1,
    "Cerebellar_ataxia|Dyskinesia|Intellectual_disability|_mild|Global_developmental_delay|Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_movement_or_behavioral_abnormalities|Dystonia_34|_myoclonic|KCNN2-related_disorder": 1,
    "not_provided|TRIM36-related_disorder": 1,
    "Anencephaly_1": 2,
    "Anencephaly": 1,
    "TRIM36-related_disorder": 7,
    "FEM1C-related_condition": 1,
    "CDO1-related_disorder": 1,
    "Delayed_puberty|_self-limited": 3,
    "DMXL1-related_disorder|not_provided": 10,
    "DMXL1-related_disorder": 56,
    "DMXL1-related_disorder|not_specified": 2,
    "not_provided|DMXL1-related_disorder": 6,
    "not_specified|DMXL1-related_disorder|not_provided": 1,
    "DMXL1-related_disorder|not_specified|not_provided": 1,
    "Perrault_syndrome_1|Bifunctional_peroxisomal_enzyme_deficiency": 16,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1": 41,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome_1": 11,
    "HSD17B4-related_disorder": 23,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 450,
    "Bifunctional_peroxisomal_enzyme_deficiency": 134,
    "Inborn_genetic_diseases|not_specified|not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 284,
    "not_provided|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 6,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 18,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|HSD17B4-related_disorder|Perrault_syndrome_1|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|HSD17B4-related_disorder|not_provided": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|Perrault_syndrome": 6,
    "not_provided|HSD17B4-related_disorder": 5,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Inborn_genetic_diseases": 5,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|Inborn_genetic_diseases|Perrault_syndrome": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1": 4,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided": 13,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_provided": 1,
    "not_provided|not_specified|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1": 7,
    "Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder": 1,
    "not_specified|HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 1,
    "Inborn_genetic_diseases|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_specified": 1,
    "not_provided|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_specified": 5,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided|Perrault_syndrome_1": 2,
    "not_specified|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 4,
    "Perrault_syndrome|not_provided|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome": 1,
    "not_provided|not_specified|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_specified": 1,
    "not_specified|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|HSD17B4-related_disorder": 4,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome|Perrault_syndrome_1|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|HSD17B4-related_disorder": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided": 9,
    "not_provided|Perrault_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 2,
    "not_specified|Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome|Perrault_syndrome_1": 1,
    "Perrault_syndrome_1|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 4,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_provided": 1,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1": 3,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_provided|Perrault_syndrome": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Inborn_genetic_diseases": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_provided": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided|Perrault_syndrome_1|not_specified": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided|HSD17B4-related_disorder": 1,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency": 3,
    "Perrault_syndrome_1|Bifunctional_peroxisomal_enzyme_deficiency|not_provided|HSD17B4-related_disorder|Perrault_syndrome": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1": 1,
    "not_specified|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "not_specified|Perrault_syndrome_1|Perrault_syndrome": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_specified": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|not_provided|HSD17B4-related_disorder|not_specified": 1,
    "HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases": 4,
    "not_specified|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|not_provided|not_specified": 1,
    "not_specified|HSD17B4-related_disorder|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome_1": 1,
    "not_provided|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_specified": 2,
    "HSD17B4-related_disorder|not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 2,
    "Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder|Perrault_syndrome|Perrault_syndrome_1": 1,
    "Inborn_genetic_diseases|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided": 2,
    "HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|Perrault_syndrome|not_provided": 1,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|not_specified": 2,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|HSD17B4-related_disorder|not_provided": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome_1|not_specified": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|HSD17B4-related_disorder|not_specified|Perrault_syndrome_1|not_provided": 1,
    "Perrault_syndrome_1|not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 2,
    "HSD17B4-related_disorder|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 4,
    "not_provided|Perrault_syndrome_1|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 5,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome|not_specified|Perrault_syndrome_1": 1,
    "HSD17B4-related_disorder|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder|Perrault_syndrome|not_provided|Perrault_syndrome_1": 1,
    "HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided": 1,
    "not_specified|Perrault_syndrome_1|not_provided|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases|Perrault_syndrome_1|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_specified|Perrault_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder": 1,
    "not_provided|not_specified|HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder|Perrault_syndrome": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_specified|Perrault_syndrome_1|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases|Perrault_syndrome_1|not_specified|not_provided|HSD17B4-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_specified|Perrault_syndrome_1|not_provided": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Rare_genetic_deafness|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|HSD17B4-related_disorder|not_specified|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder|Perrault_syndrome|not_specified|Perrault_syndrome_1": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|HSD17B4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|Inborn_genetic_diseases|not_specified|not_provided|Perrault_syndrome_1": 1,
    "not_provided|Bifunctional_peroxisomal_enzyme_deficiency|not_specified|Perrault_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "HSD17B4-related_disorder|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_specified|Perrault_syndrome|Perrault_syndrome_1|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|HSD17B4-related_disorder|not_provided|Perrault_syndrome|Inborn_genetic_diseases": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|not_provided": 1,
    "not_provided|HSD17B4-related_disorder|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_specified|not_provided": 1,
    "Perrault_syndrome_1|Inborn_genetic_diseases": 1,
    "Perrault_syndrome_1|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided|HSD17B4-related_disorder|not_specified": 1,
    "not_provided|HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome": 2,
    "not_specified|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome_1|not_provided|Perrault_syndrome": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "HSD17B4-related_disorder|not_provided|Perrault_syndrome_1|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Perrault_syndrome_1|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases|HSD17B4-related_disorder|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_specified|not_provided|Perrault_syndrome_1": 1,
    "Inborn_genetic_diseases|Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|not_provided": 1,
    "Perrault_syndrome_1|not_provided|Bifunctional_peroxisomal_enzyme_deficiency": 1,
    "Perrault_syndrome|Bifunctional_peroxisomal_enzyme_deficiency|HSD17B4-related_disorder": 1,
    "HSD17B4-related_disorder|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Inborn_genetic_diseases|not_provided|Perrault_syndrome_1": 1,
    "not_specified|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|not_provided|Perrault_syndrome_1": 1,
    "not_specified|Bifunctional_peroxisomal_enzyme_deficiency|Perrault_syndrome|Perrault_syndrome_1|not_provided": 1,
    "Bifunctional_peroxisomal_enzyme_deficiency|not_provided|Perrault_syndrome_1|not_specified": 1,
    "LOX-related_disorder|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_10|not_provided": 9,
    "not_provided|Aortic_aneurysm|_familial_thoracic_10": 4,
    "Connective_tissue_disorder|Cardiovascular_phenotype|not_provided": 1,
    "LOX-related_disorder|Cardiovascular_phenotype": 1,
    "Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype|not_provided": 6,
    "Aortic_aneurysm|_familial_thoracic_10": 14,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_10|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|LOX-related_disorder|not_provided": 1,
    "Generalized_arterial_tortuosity|Cutis_laxa": 1,
    "LOX-related_disorder": 5,
    "not_provided|LOX-related_disorder": 1,
    "not_provided|LOX-related_disorder|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|LOX-related_disorder|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_10": 1,
    "not_provided|Cardiovascular_phenotype|LOX-related_disorder": 4,
    "not_provided|Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_10|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta": 2,
    "not_provided|Abnormal_facial_shape|Pleural_effusion|Increased_number_of_skin_folds|Emphysema|Interphalangeal_joint_contracture_of_finger": 1,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|not_provided": 1,
    "LOX-related_disorder|not_specified|not_provided": 1,
    "LOX-related_disorder|Cardiovascular_phenotype|not_provided": 2,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype|LOX-related_disorder": 2,
    "not_provided|not_specified|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_10": 1,
    "Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "LOX_POLYMORPHISM|Cardiovascular_phenotype|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_provided|LOX-related_disorder": 1,
    "LOX-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_10|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype|not_provided|LOX-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_10|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_10": 2,
    "not_provided|not_specified|LOX-related_disorder|Cardiovascular_phenotype": 1,
    "Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_10|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_10|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cardiovascular_phenotype": 2,
    "Aortic_aneurysm|_familial_thoracic_10|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta": 1,
    "Parkinson_Disease|_Dominant/Recessive|not_provided": 12,
    "not_specified|Parkinson_Disease|_Dominant/Recessive": 1,
    "Parkinson_Disease|_Dominant/Recessive|not_specified": 3,
    "Parkinson_Disease|_Dominant/Recessive|not_provided|Parkinson_disease|_late-onset": 1,
    "not_specified|not_provided|Parkinson_Disease|_Dominant/Recessive": 1,
    "PRDM6-related_disorder": 10,
    "Familial_patent_arterial_duct": 1,
    "not_provided|PRDM6-related_disorder": 3,
    "Patent_ductus_arteriosus_3|Inborn_genetic_diseases": 1,
    "Patent_ductus_arteriosus_3": 9,
    "Inborn_genetic_diseases|PRDM6-related_disorder": 2,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 264,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_provided": 21,
    "not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 23,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|CEP120-related_disorder": 6,
    "Joubert_syndrome_31|not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 10,
    "not_provided|CEP120-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Joubert_syndrome_31|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|CEP120-related_disorder|not_provided": 1,
    "Joubert_syndrome_31": 8,
    "CEP120-related_disorder|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Inborn_genetic_diseases|not_provided": 1,
    "CEP120-related_disorder|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 7,
    "CEP120-related_disorder|Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Inborn_genetic_diseases": 9,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_specified|not_provided": 2,
    "not_provided|CEP120-related_disorder|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "Joubert_syndrome_31|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|CEP120-related_disorder|not_provided": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_provided|Inborn_genetic_diseases": 2,
    "CEP120-related_disorder|not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Joubert_syndrome_31|not_provided": 1,
    "not_provided|Joubert_syndrome_31|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "not_specified|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|CEP120-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 2,
    "CEP120-related_disorder": 4,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Joubert_syndrome_31|not_provided": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Joubert_syndrome_31": 2,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 4,
    "not_provided|CEP120-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_provided|Joubert_syndrome_31|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_31|Inborn_genetic_diseases|not_specified|CEP120-related_disorder|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|CEP120-related_disorder|not_specified": 1,
    "Joubert_syndrome_31|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "Inborn_genetic_diseases|not_provided|CEP120-related_disorder|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Chuvash_polycythemia": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_provided": 3,
    "not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_specified": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_specified": 1,
    "not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|Inborn_genetic_diseases|CEP120-related_disorder": 1,
    "not_provided|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_specified": 1,
    "CSNK1G3-related_disorder": 4,
    "Pyridoxine-dependent_epilepsy": 696,
    "not_provided|Pyridoxine-dependent_epilepsy": 53,
    "Pyridoxine-dependent_epilepsy|not_provided": 41,
    "Pyridoxine-dependent_epilepsy|not_specified|not_provided": 5,
    "not_specified|Pyridoxine-dependent_epilepsy": 20,
    "Pyridoxine-dependent_epilepsy|Abnormality_of_the_nervous_system|not_provided": 1,
    "Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy": 16,
    "Inborn_genetic_diseases|not_specified|not_provided|Pyridoxine-dependent_epilepsy": 4,
    "not_provided|Ventriculomegaly|Seizure|Pyridoxine-dependent_epilepsy_caused_by_ALDH7A1_mutant|Pyridoxine-dependent_epilepsy|ALDH7A1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Pyridoxine-dependent_epilepsy": 6,
    "Pyridoxine-dependent_epilepsy|not_specified": 28,
    "not_specified|not_provided|Pyridoxine-dependent_epilepsy": 6,
    "Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases": 24,
    "Intellectual_disability|Pyridoxine-dependent_epilepsy": 1,
    "Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy|not_provided": 5,
    "Epilepsy|Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Pyridoxine-dependent_epilepsy|Intellectual_disability": 1,
    "ALDH7A1-related_disorder|Pyridoxine-dependent_epilepsy": 1,
    "not_specified|Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy": 3,
    "not_provided|not_specified|Pyridoxine-dependent_epilepsy": 2,
    "ALDH7A1-related_disorder|not_specified|Pyridoxine-dependent_epilepsy": 1,
    "Pyridoxine-dependent_epilepsy_caused_by_ALDH7A1_mutant|not_provided|Pyridoxine-dependent_epilepsy|Seizure": 1,
    "not_provided|Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy": 4,
    "Pyridoxine-dependent_epilepsy|not_provided|not_specified": 1,
    "Pyridoxine-dependent_epilepsy|Seizure": 2,
    "Pyridoxine-dependent_epilepsy|ALDH7A1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Pyridoxine-dependent_epilepsy|not_specified|Leukoencephalopathy": 1,
    "Pyridoxine-dependent_epilepsy|Developmental_and_epileptic_encephalopathy|_1": 1,
    "not_provided|ALDH7A1-related_disorder|Pyridoxine-dependent_epilepsy": 1,
    "not_specified|ALDH7A1-related_disorder|Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy|not_provided": 1,
    "not_provided|ALDH7A1-related_disorder|Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy": 1,
    "Pyridoxine-dependent_epilepsy|not_provided|Inborn_genetic_diseases": 4,
    "Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases|not_provided": 2,
    "ALDH7A1-related_disorder|Inborn_genetic_diseases|not_provided|Seizure|Pyridoxine-dependent_epilepsy": 1,
    "Pyridoxine-dependent_epilepsy|See_cases|not_provided": 1,
    "ALDH7A1-related_disorder|not_provided|Pyridoxine-dependent_epilepsy": 2,
    "Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy|not_specified": 2,
    "Inborn_genetic_diseases|ALDH7A1-related_disorder|not_specified|not_provided|Pyridoxine-dependent_epilepsy": 1,
    "not_provided|Seizure|ALDH7A1-related_disorder|Developmental_and_epileptic_encephalopathy|_13|Pyridoxine-dependent_epilepsy": 1,
    "Pyridoxine-dependent_epilepsy|not_provided|ALDH7A1-related_disorder": 1,
    "Pyridoxine-dependent_epilepsy|Abnormal_brain_morphology": 1,
    "ALDH7A1-related_disorder|not_provided|Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases": 1,
    "See_cases|Pyridoxine-dependent_epilepsy": 1,
    "Pyridoxine-dependent_epilepsy|See_cases": 1,
    "not_provided|Pyridoxine-dependent_epilepsy|ALDH7A1-related_disorder": 1,
    "Pyridoxine-dependent_epilepsy|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Pyridoxine-dependent_epilepsy|not_specified|not_provided": 2,
    "Pyridoxine-dependent_epilepsy|not_provided|Ventriculomegaly|Seizure|See_cases|Inborn_genetic_diseases": 1,
    "Pyridoxine-dependent_epilepsy|Neonatal_seizure|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Pyridoxine-dependent_epilepsy|Intractable_seizure": 1,
    "not_specified|Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases": 1,
    "ALDH7A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Pyridoxine-dependent_epilepsy": 1,
    "Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Pyridoxine-dependent_epilepsy|not_provided": 1,
    "ALDH7A1-related_disorder|Pyridoxine-dependent_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "Leukodystrophy|_Adult-Onset": 14,
    "Leukodystrophy|_Adult-Onset|not_provided": 1,
    "Adult-onset_autosomal_dominant_demyelinating_leukodystrophy": 28,
    "LMNB1-related_disorder|not_provided": 5,
    "Adult-onset_autosomal_dominant_demyelinating_leukodystrophy|not_provided": 12,
    "LMNB1-related_primary_microcephaly|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_26|_primary|_autosomal_dominant|Syndrome_with_microcephaly_as_major_feature": 1,
    "Syndrome_with_microcephaly_as_major_feature|not_provided|Microcephaly_26|_primary|_autosomal_dominant": 1,
    "Microcephaly_26|_primary|_autosomal_dominant": 6,
    "not_provided|Adult-onset_autosomal_dominant_demyelinating_leukodystrophy|Microcephaly_26|_primary|_autosomal_dominant": 1,
    "LMNB1-related_disorder": 4,
    "not_provided|Adult-onset_autosomal_dominant_demyelinating_leukodystrophy": 8,
    "not_specified|Adult-onset_autosomal_dominant_demyelinating_leukodystrophy|not_provided": 2,
    "Microcephaly_26|_primary|_autosomal_dominant|Syndrome_with_microcephaly_as_major_feature": 2,
    "Adult-onset_autosomal_dominant_demyelinating_leukodystrophy|Inborn_genetic_diseases": 1,
    "Microcephaly_26|_primary|_autosomal_dominant|Syndrome_with_microcephaly_as_major_feature|Inborn_genetic_diseases": 1,
    "Adult-onset_autosomal_dominant_demyelinating_leukodystrophy|Microcephaly_26|_primary|_autosomal_dominant|not_provided": 1,
    "Microcephaly_26|_primary|_autosomal_dominant|LMNB1-related_disorder|Inborn_genetic_diseases": 1,
    "LMNB1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "MEGF10-related_myopathy": 662,
    "MEGF10-related_myopathy|not_provided": 37,
    "MEGF10-related_myopathy|not_specified": 17,
    "not_provided|MEGF10-related_myopathy": 37,
    "Inborn_genetic_diseases|not_specified|MEGF10-related_myopathy": 1,
    "not_specified|MEGF10-related_myopathy": 11,
    "not_specified|MEGF10-related_myopathy|not_provided": 8,
    "MEGF10-related_myopathy|not_provided|MEGF10-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|MEGF10-related_myopathy": 6,
    "MEGF10-related_myopathy|MEGF10-related_disorder": 3,
    "Congenital_myopathy_10b|_mild_variant|MEGF10-related_myopathy": 3,
    "not_specified|not_provided|MEGF10-related_myopathy": 4,
    "MEGF10-related_myopathy|Inborn_genetic_diseases|not_provided": 6,
    "MEGF10-related_myopathy|Inborn_genetic_diseases": 32,
    "Congenital_myopathy_10b|_mild_variant": 9,
    "Inborn_genetic_diseases|MEGF10-related_myopathy": 30,
    "not_provided|Inborn_genetic_diseases|MEGF10-related_myopathy": 3,
    "MEGF10-related_disorder|MEGF10-related_myopathy|not_specified": 1,
    "Inborn_genetic_diseases|MEGF10-related_myopathy|not_specified": 1,
    "MEGF10-related_disorder": 2,
    "Inborn_genetic_diseases|MEGF10-related_myopathy|not_provided": 3,
    "MEGF10-related_disorder|not_provided|not_specified|MEGF10-related_myopathy": 1,
    "MEGF10-related_disorder|MEGF10-related_myopathy": 4,
    "MEGF10-related_myopathy|Congenital_myopathy_10b|_mild_variant": 4,
    "Inborn_genetic_diseases|MEGF10-related_disorder|not_provided": 1,
    "MEGF10-related_disorder|not_specified|MEGF10-related_myopathy|not_provided": 1,
    "MEGF10-related_myopathy|MEGF10-related_disorder|not_provided": 2,
    "MEGF10-related_myopathy|MEGF10-related_disorder|not_provided|not_specified": 1,
    "MEGF10-related_disorder|MEGF10-related_myopathy|not_provided": 2,
    "not_provided|MEGF10-related_myopathy|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|MEGF10-related_myopathy|not_provided|MEGF10-related_disorder": 1,
    "not_provided|Congenital_myopathy_10b|_mild_variant|MEGF10-related_myopathy": 1,
    "MEGF10-related_disorder|not_provided|MEGF10-related_myopathy": 1,
    "MEGF10-related_myopathy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|MEGF10-related_myopathy|MEGF10-related_disorder": 1,
    "MEGF10-related_myopathy|not_specified|not_provided": 2,
    "not_specified|not_provided|MEGF10-related_disorder|MEGF10-related_myopathy": 1,
    "MEGF10-related_myopathy|MEGF10-related_disorder|Inborn_genetic_diseases": 1,
    "SLC12A2-related_disorder|not_provided": 2,
    "Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|Kilquist_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Delpire-McNeill_syndrome|Kilquist_syndrome|Hearing_loss|_autosomal_dominant_78|not_provided": 1,
    "Delpire-McNeill_syndrome": 19,
    "Inborn_genetic_diseases|Kilquist_syndrome|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|Kilquist_syndrome|SLC12A2-related_disorder": 2,
    "not_specified|Delpire-McNeill_syndrome|Hearing_loss|_autosomal_dominant_78|Kilquist_syndrome|not_provided": 1,
    "Kilquist_syndrome|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|not_provided": 14,
    "not_provided|SLC12A2-related_disorder": 2,
    "SLC12A2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Kilquist_syndrome|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Kilquist_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "SLC12A2-related_disorder": 11,
    "Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|Kilquist_syndrome|not_provided": 5,
    "Kilquist_syndrome": 6,
    "Delpire-McNeill_syndrome|not_provided": 1,
    "not_provided|Kilquist_syndrome|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome": 4,
    "Inborn_genetic_diseases|SLC12A2-related_disorder": 1,
    "not_provided|Kilquist_syndrome|Delpire-McNeill_syndrome": 2,
    "not_provided|Delpire-McNeill_syndrome": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome|Kilquist_syndrome": 2,
    "Profound_global_developmental_delay": 1,
    "Kilquist_syndrome|Hearing_loss|_autosomal_dominant_78|Delpire-McNeill_syndrome": 3,
    "Hearing_loss|_autosomal_dominant_78": 5,
    "Hearing_loss|Hearing_loss|_autosomal_dominant_78": 2,
    "Hearing_loss|not_provided|Hearing_loss|_autosomal_dominant_78": 1,
    "Hearing_loss|_autosomal_dominant_78|Kilquist_syndrome|Delpire-McNeill_syndrome|Hearing_loss": 1,
    "Infant_onset_multiple_organ_failure": 1,
    "Inborn_genetic_diseases|Kilquist_syndrome": 1,
    "Intellectual_disability|SLC12A2-related_disorder": 1,
    "Congenital_contractural_arachnodactyly": 1533,
    "Congenital_contractural_arachnodactyly|not_provided": 121,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|Connective_tissue_disorder|not_specified": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 43,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 96,
    "not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 25,
    "not_provided|Congenital_contractural_arachnodactyly": 127,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 15,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|Macular_degeneration|_early-onset": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 164,
    "Congenital_contractural_arachnodactyly|not_provided|Macular_degeneration|_early-onset|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_contractural_arachnodactyly": 28,
    "Congenital_contractural_arachnodactyly|Cardiovascular_phenotype": 4,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|FBN2-related_disorder|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided": 25,
    "not_provided|Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Congenital_contractural_arachnodactyly|Cardiovascular_phenotype|not_specified": 1,
    "FBN2-related_disorder": 33,
    "Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 34,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified|not_provided|FBN2-related_disorder|Macular_degeneration|_early-onset": 1,
    "not_provided|Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 1,
    "not_specified|Congenital_contractural_arachnodactyly": 37,
    "Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_provided": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified|not_provided|Connective_tissue_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly": 11,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|FBN2-related_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|not_specified": 28,
    "Congenital_contractural_arachnodactyly|FBN2-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Connective_tissue_disorder|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|See_cases": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly|not_provided": 6,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|Connective_tissue_disorder|not_specified|not_provided": 1,
    "not_provided|FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Connective_tissue_disorder|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Macular_degeneration|_early-onset|Ehlers-Danlos_syndrome|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 2,
    "not_specified|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_specified|Congenital_contractural_arachnodactyly|not_provided": 5,
    "Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 6,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly": 4,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 3,
    "Congenital_contractural_arachnodactyly|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN2-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|FBN2-related_disorder|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 7,
    "FBN2-related_disorder|Congenital_contractural_arachnodactyly": 7,
    "FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 4,
    "FBN2-related_disorder|not_provided|Congenital_contractural_arachnodactyly": 1,
    "not_provided|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_provided": 6,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 8,
    "not_specified|not_provided|Congenital_contractural_arachnodactyly": 5,
    "not_provided|not_specified|Congenital_contractural_arachnodactyly": 4,
    "Congenital_contractural_arachnodactyly|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified|not_provided": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_provided|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|FBN2-related_disorder|Connective_tissue_disorder": 1,
    "Short_stature|Decreased_body_weight|Facial_asymmetry|Strabismus|Global_developmental_delay|Single_transverse_palmar_crease|Ventricular_septal_defect": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided": 3,
    "FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly": 1,
    "not_provided|FBN2-related_disorder|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified": 1,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN2-related_disorder|Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|not_specified|Congenital_contractural_arachnodactyly": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome": 5,
    "FBN2-related_disorder|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Congenital_contractural_arachnodactyly|not_provided|not_specified": 3,
    "FBN2-related_disorder|Ehlers-Danlos_syndrome|not_provided|not_specified|Congenital_contractural_arachnodactyly": 1,
    "FBN2-related_disorder|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified": 10,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 1,
    "Connective_tissue_disorder|Congenital_contractural_arachnodactyly": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_specified|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|Craniosynostosis_syndrome|not_specified|Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|not_specified|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|FBN2-related_disorder": 8,
    "Congenital_contractural_arachnodactyly|not_provided|not_specified|Macular_degeneration|_early-onset": 1,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|Congenital_contractural_arachnodactyly": 3,
    "not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 5,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|not_provided": 3,
    "not_specified|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_specified|not_provided|FBN2-related_disorder": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_provided|not_specified": 1,
    "FBN2-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified": 2,
    "not_specified|Congenital_contractural_arachnodactyly|FBN2-related_disorder|not_provided": 1,
    "not_provided|Congenital_contractural_arachnodactyly|not_specified": 3,
    "Congenital_contractural_arachnodactyly|not_specified|not_provided": 4,
    "Connective_tissue_disorder|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder|not_specified": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "Inborn_genetic_diseases|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|not_specified|Congenital_contractural_arachnodactyly": 1,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|Cardiovascular_phenotype|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified|FBN2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN2-related_disorder|Congenital_contractural_arachnodactyly": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Neurodevelopmental_abnormality|Congenital_contractural_arachnodactyly": 1,
    "not_specified|Congenital_contractural_arachnodactyly|not_provided|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder": 1,
    "not_specified|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|not_specified|not_provided|Nonsyndromic_Heritable_Thoracic_Aortic_Aneurysms_And_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder": 3,
    "Congenital_contractural_arachnodactyly|not_provided|Ehlers-Danlos_syndrome": 1,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_provided|not_specified": 1,
    "FBN2-related_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|FBN2-related_disorder": 3,
    "not_specified|Connective_tissue_disorder|Congenital_contractural_arachnodactyly": 1,
    "Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly|FBN2-related_disorder": 1,
    "not_specified|Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Macular_degeneration|_early-onset|not_provided|Congenital_contractural_arachnodactyly": 1,
    "not_provided|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|not_specified|not_provided|Connective_tissue_disorder|Macular_degeneration|_early-onset": 1,
    "Congenital_contractural_arachnodactyly|not_specified|Connective_tissue_disorder": 2,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Congenital_contractural_arachnodactyly": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder": 3,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 2,
    "not_provided|FBN2-related_disorder|Inborn_genetic_diseases|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder": 1,
    "Cardiovascular_phenotype|Congenital_contractural_arachnodactyly|not_provided": 1,
    "Macular_degeneration|_early-onset": 5,
    "Congenital_contractural_arachnodactyly|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|FBN2-related_disorder|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_specified|Congenital_contractural_arachnodactyly": 1,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|Connective_tissue_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder": 2,
    "Connective_tissue_disorder|not_provided|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 4,
    "not_provided|FBN2-related_disorder": 1,
    "not_specified|FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided": 1,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly": 1,
    "not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly": 2,
    "Ehlers-Danlos_syndrome|not_specified|Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified|Connective_tissue_disorder": 1,
    "Congenital_contractural_arachnodactyly|Marfan_syndrome": 2,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_provided": 1,
    "Congenital_contractural_arachnodactyly|Connective_tissue_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder": 3,
    "Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder|Macular_degeneration|_early-onset|not_specified": 1,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|FBN2-related_disorder|not_specified|not_provided": 1,
    "Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_specified|not_provided|Congenital_contractural_arachnodactyly": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|Connective_tissue_disorder|not_specified|not_provided": 1,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 1,
    "not_provided|not_specified|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|not_provided|not_specified|FBN2-related_disorder": 1,
    "Macular_degeneration|_early-onset|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder": 3,
    "Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|Connective_tissue_disorder": 2,
    "Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Macular_degeneration|_early-onset": 2,
    "not_provided|Congenital_contractural_arachnodactyly|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|Macular_degeneration|_early-onset|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Connective_tissue_disorder|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Congenital_contractural_arachnodactyly|Cardiovascular_phenotype|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_provided": 1,
    "Arterial_dissection": 1,
    "Congenital_contractural_arachnodactyly|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Congenital_contractural_arachnodactyly|Connective_tissue_disorder|not_specified": 1,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder": 3,
    "not_specified|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Connective_tissue_disorder|not_specified|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder": 1,
    "not_provided|Congenital_contractural_arachnodactyly|FBN2-related_disorder": 2,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|not_specified|not_provided|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|FBN2-related_disorder|not_specified|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Connective_tissue_disorder|FBN2-related_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_contractural_arachnodactyly": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|Macular_degeneration|_early-onset": 1,
    "FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Congenital_contractural_arachnodactyly|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_specified|Congenital_contractural_arachnodactyly|not_provided": 1,
    "not_provided|Congenital_heart_disease|Congenital_contractural_arachnodactyly": 1,
    "Connective_tissue_disorder|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "not_specified|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|Connective_tissue_disorder|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|FBN2-related_disorder|not_specified|Ehlers-Danlos_syndrome": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Loeys-Dietz_syndrome|Aortic_aneurysm|_familial_thoracic_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Congenital_contractural_arachnodactyly": 3,
    "FBN2-related_disorder|Connective_tissue_disorder|Brain_aneurysm|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "not_specified|Congenital_contractural_arachnodactyly|Connective_tissue_disorder|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|not_provided|not_specified|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Macular_degeneration|_early-onset|Congenital_contractural_arachnodactyly": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|_type_4": 1,
    "not_provided|Congenital_contractural_arachnodactyly|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN2-related_disorder|not_specified": 1,
    "not_provided|Congenital_contractural_arachnodactyly|not_specified|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|FBN2-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Macular_degeneration|_early-onset": 1,
    "FBN2-related_disorder|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_specified|not_provided|Connective_tissue_disorder|Macular_degeneration|_early-onset": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FBN2-related_disorder|Congenital_contractural_arachnodactyly": 1,
    "not_specified|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN2-related_disorder|Congenital_contractural_arachnodactyly|not_specified": 1,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|not_provided": 1,
    "FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Neonatal_death|Fetal_akinesia_deformation_sequence_1|Cerebral_ischemia": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly": 2,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|not_provided": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Congenital_contractural_arachnodactyly": 1,
    "not_provided|Congenital_contractural_arachnodactyly|High_myopia": 1,
    "FBN2-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|FBN2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Congenital_contractural_arachnodactyly|Connective_tissue_disorder": 1,
    "Connective_tissue_disorder|FBN2-related_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN2-related_disorder": 1,
    "FBN2-related_disorder|not_specified|not_provided|Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Congenital_contractural_arachnodactyly|FBN2-related_disorder": 1,
    "not_specified|Congenital_contractural_arachnodactyly|not_provided|Connective_tissue_disorder": 1,
    "not_provided|Congenital_contractural_arachnodactyly|Macular_degeneration|_early-onset": 1,
    "Ehlers-Danlos_syndrome|Congenital_contractural_arachnodactyly|not_provided|FBN2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Congenital_contractural_arachnodactyly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Macular_degeneration|_early-onset": 1,
    "Congenital_contractural_arachnodactyly|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Inborn_genetic_diseases|ADAMTS19-related_disorder": 2,
    "ADAMTS19-related_disorder": 6,
    "Cardiac_valvular_dysplasia_2": 8,
    "ADAMTS19-associated_congenital_heartdefect": 1,
    "MINAR2-related_condition": 3,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 63,
    "Charcot-Marie-Tooth_disease|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 1,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|not_specified|Inborn_genetic_diseases|HINT1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 1,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|not_provided": 1,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|not_provided|Peripheral_neuropathy": 1,
    "Sensory_axonal_neuropathy": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 2,
    "HINT1-related_disorder|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 4,
    "not_specified|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 1,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|not_specified": 4,
    "Autosomal_recessive_axonal_neuropathy_with_neuromyotonia|Inborn_genetic_diseases|not_provided|Peripheral_neuropathy": 1,
    "not_provided|Autosomal_recessive_axonal_neuropathy_with_neuromyotonia": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_8": 11,
    "Mitochondrial_complex_III_deficiency_nuclear_type_8|not_provided": 3,
    "LYRM7-related_disorder|not_provided": 2,
    "Immunodeficiency_93_and_hypertrophic_cardiomyopathy": 5,
    "FNIP1-related_disorder": 1,
    "not_provided|FNIP1-related_disorder": 1,
    "Immunodeficiency_93_and_hypertrophic_cardiomyopathy|not_provided": 1,
    "ACSL6-related_disorder": 10,
    "ACSL6-related_disorder|not_provided": 1,
    "Myopia_25|_autosomal_dominant": 4,
    "Myopia_25|_autosomal_dominant|not_provided": 1,
    "not_provided|P4HA2-related_disorder": 3,
    "P4HA2-related_disorder|not_provided": 1,
    "P4HA2-related_disorder": 8,
    "not_specified|Myopia_25|_autosomal_dominant": 1,
    "Myopia_25|_autosomal_dominant|not_specified": 2,
    "not_provided|Myopia_25|_autosomal_dominant": 1,
    "P4HA2-related_disorder|Myopia_25|_autosomal_dominant|not_provided": 1,
    "BONE_MINERAL_DENSITY_QUANTITATIVE_TRAIT_LOCUS_15": 2,
    "SLC22A4-related_disorder": 5,
    "not_provided|SLC22A4-related_disorder": 7,
    "not_specified|SLC22A4-related_disorder": 2,
    "SLC22A4-related_disorder|not_specified|not_provided": 1,
    "SLC22A4-related_disorder|not_provided": 1,
    "SLC22A4-related_disorder|not_specified": 1,
    "not_provided|SLC22A4_POLYMORPHISM": 1,
    "Renal_carnitine_transport_defect|not_provided": 36,
    "Inflammatory_bowel_disease_5": 1,
    "SLC22A5-related_disorder|Inborn_genetic_diseases|not_provided|Renal_carnitine_transport_defect": 3,
    "not_specified|Renal_carnitine_transport_defect|not_provided": 3,
    "Renal_carnitine_transport_defect|not_specified|not_provided": 6,
    "not_specified|Renal_carnitine_transport_defect": 15,
    "Renal_carnitine_transport_defect|Inborn_genetic_diseases": 13,
    "Carnitine_deficiency": 29,
    "SLC22A5-related_disorder|Renal_carnitine_transport_defect": 6,
    "Decreased_circulating_carnitine_concentration|Renal_carnitine_transport_defect": 27,
    "Inborn_genetic_diseases|Renal_carnitine_transport_defect": 9,
    "Decreased_circulating_carnitine_concentration|not_provided|Renal_carnitine_transport_defect": 9,
    "not_provided|Renal_carnitine_transport_defect": 52,
    "Renal_carnitine_transport_defect|Decreased_circulating_carnitine_concentration": 36,
    "Renal_carnitine_transport_defect|not_specified": 9,
    "not_provided|Renal_carnitine_transport_defect|not_specified": 4,
    "SLC22A5-related_disorder|not_provided|Renal_carnitine_transport_defect": 2,
    "Renal_carnitine_transport_defect|not_provided|not_specified": 6,
    "Renal_carnitine_transport_defect|not_provided|Decreased_circulating_carnitine_concentration": 2,
    "not_provided|Renal_carnitine_transport_defect|See_cases": 2,
    "Decreased_circulating_carnitine_concentration|Renal_carnitine_transport_defect|not_provided": 2,
    "not_provided|Decreased_circulating_carnitine_concentration|Renal_carnitine_transport_defect|Inborn_genetic_diseases": 1,
    "not_provided|Renal_carnitine_transport_defect|SLC22A5-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Carnitine_deficiency|not_provided|Renal_carnitine_transport_defect": 1,
    "Renal_carnitine_transport_defect|not_provided|Decreased_circulating_carnitine_concentration|Congenital_myasthenic_syndrome_20": 1,
    "not_provided|Renal_carnitine_transport_defect|not_specified|Decreased_circulating_carnitine_concentration": 2,
    "not_provided|Renal_carnitine_transport_defect|Decreased_circulating_carnitine_concentration": 2,
    "Renal_carnitine_transport_defect|Decreased_circulating_carnitine_concentration|Inborn_genetic_diseases": 1,
    "Decreased_circulating_carnitine_concentration|Renal_carnitine_transport_defect|SLC22A5-related_disorder": 2,
    "not_specified|not_provided|Renal_carnitine_transport_defect|Abnormality_of_the_nervous_system": 1,
    "SLC22A5-related_disorder": 2,
    "Renal_carnitine_transport_defect|Carnitine_deficiency": 5,
    "not_specified|not_provided|Renal_carnitine_transport_defect": 9,
    "not_provided|SLC22A5-related_disorder|Renal_carnitine_transport_defect": 3,
    "Carnitine_deficiency|Renal_carnitine_transport_defect": 8,
    "not_provided|Decreased_circulating_carnitine_concentration|Renal_carnitine_transport_defect": 2,
    "Renal_carnitine_transport_defect|Decreased_circulating_carnitine_concentration|not_provided": 2,
    "Renal_carnitine_transport_defect|Decreased_circulating_carnitine_concentration|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Renal_carnitine_transport_defect|SLC22A5-related_disorder": 1,
    "Inborn_genetic_diseases|Renal_carnitine_transport_defect|Decreased_circulating_carnitine_concentration": 1,
    "not_specified|Renal_carnitine_transport_defect|Inborn_genetic_diseases": 1,
    "Renal_carnitine_transport_defect|SLC22A5-related_disorder": 3,
    "Decreased_circulating_carnitine_concentration|not_provided|Dilated_cardiomyopathy_1A|Renal_carnitine_transport_defect": 1,
    "Renal_carnitine_transport_defect|Inborn_genetic_diseases|not_provided": 1,
    "Decreased_circulating_carnitine_concentration|SLC22A5-related_disorder|Inborn_genetic_diseases|not_provided|Renal_carnitine_transport_defect": 1,
    "Inborn_genetic_diseases|not_provided|Renal_carnitine_transport_defect": 1,
    "Decreased_circulating_carnitine_concentration|Renal_carnitine_transport_defect|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|SLC22A5-related_disorder|Renal_carnitine_transport_defect": 1,
    "not_provided|not_specified|Renal_carnitine_transport_defect": 1,
    "SLC22A5-related_disorder|not_specified|not_provided|Renal_carnitine_transport_defect|High_myopia": 1,
    "not_provided|Renal_carnitine_transport_defect|SLC22A5-related_disorder|not_specified": 1,
    "IRF1-related_disorder": 1,
    "Immunodeficiency_117": 2,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 125,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome": 14,
    "Neuroepithelial_tumor|_PATZ1_fusion-positive|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder|Nijmegen_breakage_syndrome-like_disorder": 2,
    "Nijmegen_breakage_syndrome-like_disorder": 28,
    "Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder|Nijmegen_breakage_syndrome-like_disorder|not_provided": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 90,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Nijmegen_breakage_syndrome-like_disorder": 5,
    "Nijmegen_breakage_syndrome-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Nijmegen_breakage_syndrome-like_disorder": 7,
    "Familial_cancer_of_breast|not_provided|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Nijmegen_breakage_syndrome-like_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "RAD50-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Myoepithelial_tumor|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder|Breast_carcinoma": 1,
    "not_specified|Nijmegen_breakage_syndrome-like_disorder|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "not_provided|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "RAD50-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Nijmegen_breakage_syndrome-like_disorder": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder": 16,
    "Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Nijmegen_breakage_syndrome-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_specified": 3,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_provided": 7,
    "not_specified|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder": 12,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder": 1,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder": 1,
    "not_provided|Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder|Ovarian_cancer|not_specified|not_provided": 1,
    "RAD50-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|RAD50-related_disorder|Familial_cancer_of_breast|not_provided|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Prostate_cancer": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder|not_provided": 1,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "RAD50-related_disorder|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 130,
    "Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|Breast_and/or_ovarian_cancer|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 2,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 23,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast": 1,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_provided|Breast_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome|Lung_sarcomatoid_carcinoma|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_specified|RAD50-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder": 1,
    "not_specified|not_provided|Premature_ovarian_insufficiency|Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|RAD50-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Breast_cancer|_susceptibility_to|Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Nijmegen_breakage_syndrome-like_disorder|not_provided": 1,
    "not_specified|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|RAD50-related_disorder": 3,
    "Nijmegen_breakage_syndrome-like_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Nijmegen_breakage_syndrome-like_disorder|not_provided": 1,
    "RAD50-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 197,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Nijmegen_breakage_syndrome-like_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Familial_cancer_of_breast|not_specified|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 7,
    "See_cases|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Neoplasm_of_the_skin|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "RAD50-related_disorder|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Nijmegen_breakage_syndrome-like_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Nijmegen_breakage_syndrome-like_disorder|Familial_cancer_of_breast": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|RAD50-related_disorder": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Nijmegen_breakage_syndrome-like_disorder|not_specified": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Nijmegen_breakage_syndrome-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Nijmegen_breakage_syndrome-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Nijmegen_breakage_syndrome-like_disorder|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Nijmegen_breakage_syndrome-like_disorder|Ovarian_cancer": 1,
    "Nijmegen_breakage_syndrome-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|Nijmegen_breakage_syndrome-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Premature_ovarian_insufficiency": 1,
    "Inherited_susceptibility_to_asthma": 4,
    "IL13-related_disorder": 2,
    "Allergic_rhinitis|_susceptibility_to|IL13-related_disorder|Inherited_susceptibility_to_asthma": 1,
    "KIF3A-related_disorder": 3,
    "SHROOM1-related_disorder|not_specified": 1,
    "Premature_ovarian_failure_14": 7,
    "Genetic_non-acquired_premature_ovarian_failure|Premature_ovarian_failure_14": 1,
    "not_specified|Premature_ovarian_failure_14": 1,
    "GDF9-related_disorder|not_provided": 1,
    "GDF9-related_disorder|not_specified": 1,
    "not_provided|GDF9-related_disorder": 2,
    "GDF9-related_disorder": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_4": 39,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_4": 3,
    "UQCRQ-related_disorder|Mitochondrial_complex_III_deficiency_nuclear_type_4|not_provided": 2,
    "UQCRQ-related_disorder": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_4|not_provided": 3,
    "not_provided|not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_4": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_4|not_specified": 2,
    "AFF4-related_disorder": 97,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 280,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder": 29,
    "AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 37,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_provided|AFF4-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 3,
    "AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_provided": 2,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_specified": 3,
    "not_provided|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 9,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_provided": 11,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|Inborn_genetic_diseases": 6,
    "AFF4-related_disorder|Inborn_genetic_diseases|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 5,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder|not_provided": 2,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder|not_specified": 1,
    "not_provided|AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|Inborn_genetic_diseases": 7,
    "AFF4-related_disorder|Inborn_genetic_diseases": 4,
    "not_specified|Inborn_genetic_diseases|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "Cornelia_de_Lange_syndrome_6": 10,
    "Inborn_genetic_diseases|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder": 4,
    "not_specified|AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "Inborn_genetic_diseases|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 9,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 4,
    "Inborn_genetic_diseases|AFF4-related_disorder": 3,
    "not_provided|AFF4-related_disorder|Inborn_genetic_diseases|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "not_provided|AFF4-related_disorder": 4,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|Inborn_genetic_diseases|AFF4-related_disorder": 5,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|Inborn_genetic_diseases|AFF4-related_disorder|not_provided": 1,
    "AFF4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "AFF4-related_disorder|not_provided": 1,
    "AFF4-related_disorder|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_specified": 1,
    "not_specified|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "Inborn_genetic_diseases|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_provided": 1,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|Inborn_genetic_diseases|AFF4-related_disorder|not_specified|not_provided": 1,
    "Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|AFF4-related_disorder|not_provided|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome": 1,
    "not_provided|Cognitive_impairment_-_coarse_facies_-_heart_defects_-_obesity_-_pulmonary_involvement_-_short_stature_-_skeletal_dysplasia_syndrome|AFF4-related_disorder": 1,
    "Keratoconus_1": 11,
    "PPP2CA-related_disorder": 6,
    "Houge-Janssens_syndrome_3": 25,
    "not_provided|Houge-Janssens_syndrome_3": 3,
    "Houge-Janssens_syndrome_3|not_provided": 4,
    "Houge-Janssens_syndrome_3|not_specified": 1,
    "not_provided|PPP2CA-related_disorder": 1,
    "UBE2B-related_disorder": 1,
    "JADE2-associated_Neurodevelopmental_Disorder": 1,
    "Chylomicron_retention_disease": 8,
    "SAR1B-related_disorder|Chylomicron_retention_disease": 1,
    "not_provided|Chylomicron_retention_disease": 5,
    "SAR1B-related_disorder": 2,
    "Inborn_genetic_diseases|Chylomicron_retention_disease": 1,
    "SAR1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Chylomicron_retention_disease|not_provided": 1,
    "not_provided|SAR1B-related_disorder": 2,
    "Progressive_spinal_muscular_atrophy": 1,
    "Congenital_disorder_of_glycosylation|_type_IIz": 2,
    "TXNDC15-related_disorder": 2,
    "Meckel_syndrome_14|Meckel-Gruber_syndrome": 2,
    "Meckel_syndrome_14|not_provided": 1,
    "not_provided|TXNDC15-related_disorder": 1,
    "Meckel_syndrome_14": 2,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 23,
    "Meckel-Gruber_syndrome|Meckel_syndrome_14": 1,
    "Brachydactyly-elbow_wrist_dysplasia_syndrome": 1,
    "not_specified|not_provided|Brachydactyly-elbow_wrist_dysplasia_syndrome|Clubfoot": 1,
    "Clubfoot": 9,
    "Micrognathia|not_specified": 1,
    "Brachydactyly-elbow_wrist_dysplasia_syndrome|Clubfoot": 1,
    "PITX1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Clubfoot": 2,
    "PITX1-related_disorder|not_provided": 1,
    "not_provided|PITX1-related_disorder": 2,
    "Clubfoot|not_specified": 1,
    "not_specified|VATER_association": 1,
    "Cranial_dysinnervation_disorder|_congenital|_with_absent_corneal_reflex_and_developmental_delay": 2,
    "Cranial_dysinnervation_disorder|_congenital|_with_absent_corneal_reflex_and_developmental_delay|See_cases": 1,
    "LECT2-related_disorder": 2,
    "Corneal_Dystrophy|_Dominant": 2,
    "Inborn_genetic_diseases|TGFBI-related_disorder": 1,
    "Corneal_dystrophy|not_provided": 26,
    "Corneal_dystrophy": 51,
    "Epithelial-stromal_TGFBI_dystrophy|Groenouw_corneal_dystrophy_type_I": 1,
    "Epithelial-stromal_TGFBI_dystrophy|not_provided|Lattice_corneal_dystrophy_Type_I": 1,
    "not_provided|Lattice_corneal_dystrophy_Type_I|Avellino_corneal_dystrophy": 1,
    "not_provided|Avellino_corneal_dystrophy|Reis-Bucklers'_corneal_dystrophy": 1,
    "Reis-Bucklers'_corneal_dystrophy|Avellino_corneal_dystrophy|Epithelial_basement_membrane_dystrophy|Lattice_corneal_dystrophy_Type_I|Corneal_dystrophy|_lattice_type_3A|Thiel-Behnke_corneal_dystrophy|Groenouw_corneal_dystrophy_type_I|Corneal_dystrophy": 1,
    "not_provided|Corneal_dystrophy|not_specified": 2,
    "TGFBI-related_disorder": 2,
    "Corneal_dystrophy|Inborn_genetic_diseases": 5,
    "not_provided|TGFBI-related_disorder|Corneal_dystrophy": 1,
    "not_provided|Corneal_dystrophy|Reis-Bucklers'_corneal_dystrophy|Avellino_corneal_dystrophy|Epithelial_basement_membrane_dystrophy|Lattice_corneal_dystrophy_Type_I|Corneal_dystrophy|_lattice_type_3A|Thiel-Behnke_corneal_dystrophy|Groenouw_corneal_dystrophy_type_I": 1,
    "TGFBI-related_disorder|Corneal_dystrophy": 2,
    "Corneal_dystrophy|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Corneal_dystrophy": 7,
    "not_provided|Corneal_dystrophy": 15,
    "Granular_corneal_dystrophy": 1,
    "Corneal_dystrophy|not_provided|not_specified": 1,
    "Lattice_corneal_dystrophy_Type_I|Avellino_corneal_dystrophy|Epithelial_basement_membrane_dystrophy|Thiel-Behnke_corneal_dystrophy|Reis-Bucklers'_corneal_dystrophy|Groenouw_corneal_dystrophy_type_I|Corneal_dystrophy|_lattice_type_3A|Corneal_dystrophy|not_specified|not_provided": 1,
    "Reis-Bucklers'_corneal_dystrophy": 3,
    "Epithelial_basement_membrane_dystrophy": 1,
    "Epithelial-stromal_TGFBI_dystrophy": 2,
    "Corneal_dystrophy|_lattice_type_3A": 1,
    "Groenouw_corneal_dystrophy_type_I|Corneal_dystrophy|_lattice_type_3A|Corneal_dystrophy": 1,
    "Corneal_dystrophy|_lattice_type_3A|Thiel-Behnke_corneal_dystrophy|Groenouw_corneal_dystrophy_type_I|Lattice_corneal_dystrophy_Type_I|Epithelial_basement_membrane_dystrophy|Reis-Bucklers'_corneal_dystrophy|Avellino_corneal_dystrophy|not_provided": 1,
    "not_provided|Thiel-Behnke_corneal_dystrophy": 1,
    "Avellino_corneal_dystrophy": 1,
    "TGFBI-related_disorder|Corneal_dystrophy|not_provided": 1,
    "Thiel-Behnke_corneal_dystrophy": 1,
    "Groenouw_corneal_dystrophy_type_I": 2,
    "not_provided|Epithelial_basement_membrane_dystrophy": 1,
    "Corneal_dystrophy|Corneal_dystrophy|_lattice_type_3A|Thiel-Behnke_corneal_dystrophy|Groenouw_corneal_dystrophy_type_I|Lattice_corneal_dystrophy_Type_I|Epithelial_basement_membrane_dystrophy|Reis-Bucklers'_corneal_dystrophy|Avellino_corneal_dystrophy|not_provided|not_specified": 1,
    "SPOCK1-related_disorder": 3,
    "Pseudohypoaldosteronism_type_2D": 85,
    "Pseudohypoaldosteronism_type_2D|Autosomal_dominant_pseudohypoaldosteronism_type_1": 58,
    "not_provided|Pseudohypoaldosteronism_type_2D|Autosomal_dominant_pseudohypoaldosteronism_type_1": 13,
    "Pseudohypoaldosteronism_type_2D|not_provided": 15,
    "Pseudohypoaldosteronism_type_2A|not_provided": 2,
    "Pseudohypoaldosteronism_type_2D|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2D": 3,
    "Pseudohypoaldosteronism_type_2D|Pseudohypoaldosteronism_type_2A|not_provided": 2,
    "not_specified|not_provided|Pseudohypoaldosteronism_type_2D|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "not_provided|Pseudohypoaldosteronism_type_2D": 3,
    "Pseudohypoaldosteronism_type_2A|not_provided|Pseudohypoaldosteronism_type_2D": 1,
    "Pseudohypoaldosteronism_type_2D|Pseudohypoaldosteronism_type_2A": 4,
    "Pseudohypoaldosteronism_type_2D|Inborn_genetic_diseases": 4,
    "KLHL3-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Pseudohypoaldosteronism_type_2D": 1,
    "Pseudohypoaldosteronism_type_2A|Pseudohypoaldosteronism_type_2D": 4,
    "not_provided|Pseudohypoaldosteronism_type_2D|Autosomal_dominant_pseudohypoaldosteronism_type_1|not_specified": 1,
    "KLHL3-related_disorder|Pseudohypoaldosteronism_type_2D|not_provided": 2,
    "Renal_tubulopathies|not_specified|Pseudohypoaldosteronism_type_2A": 1,
    "not_specified|Pseudohypoaldosteronism_type_2D": 1,
    "Pseudohypoaldosteronism_type_2D|not_provided|Pseudohypoaldosteronism_type_2A": 1,
    "not_provided|Pseudohypoaldosteronism_type_2A|Pseudohypoaldosteronism_type_2D": 1,
    "not_provided|not_specified|Pseudohypoaldosteronism_type_2D|Autosomal_dominant_pseudohypoaldosteronism_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2D": 1,
    "Pseudohypoaldosteronism_type_2D|not_provided|Inborn_genetic_diseases": 1,
    "KLHL3-related_disorder|not_provided|Pseudohypoaldosteronism_type_2D": 1,
    "Pseudohypoaldosteronism_type_2D|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|KLHL3-related_disorder": 1,
    "Myofibrillar_myopathy_3": 258,
    "not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_myopathy_3": 3,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|Myofibrillar_myopathy_3": 7,
    "not_provided|Myofibrillar_myopathy_3": 24,
    "Myofibrillar_myopathy_3|not_provided": 15,
    "Myofibrillar_myopathy_3|Inborn_genetic_diseases": 11,
    "MYOT-related_disorder|not_specified|not_provided|Myofibrillar_myopathy_3": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|not_provided|not_specified|Myofibrillar_myopathy_3": 1,
    "not_provided|Myofibrillar_myopathy_3|Distal_amyotrophy|Fatty_replacement_of_skeletal_muscle|EMG:_myopathic_abnormalities|Foot_dorsiflexor_weakness|Distal_lower_limb_muscle_weakness|Muscle_fiber_inclusion_bodies|Lower_limb_pain|Urinary_bladder_sphincter_dysfunction|Progressive_distal_muscle_weakness|Progressive_proximal_muscle_weakness": 1,
    "Distal_myopathy|Myofibrillar_myopathy|not_provided|Myofibrillar_myopathy_3": 1,
    "MYOT-related_disorder|not_provided|Myofibrillar_myopathy_3": 1,
    "not_specified|not_provided|Myofibrillar_myopathy_3": 2,
    "Inborn_genetic_diseases|Myofibrillar_myopathy_3": 12,
    "not_specified|Myofibrillar_myopathy_3|not_provided": 4,
    "Myofibrillar_myopathy_3|not_provided|Inborn_genetic_diseases": 1,
    "Heart_failure|not_specified|Myofibrillar_myopathy_3|Inborn_genetic_diseases|not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Inborn_genetic_diseases|Myofibrillar_Myopathy|_Dominant|not_specified|Myofibrillar_myopathy_3": 1,
    "Inborn_genetic_diseases|Heart_failure|Myofibrillar_myopathy_3": 1,
    "MYOT-related_disorder|not_specified|not_provided|Myofibrillar_myopathy_3|Heart_failure": 1,
    "not_provided|Inborn_genetic_diseases|Myofibrillar_myopathy_3": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Myofibrillar_myopathy_3": 1,
    "not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|MYOT-related_disorder|Myofibrillar_Myopathy|_Dominant|Inborn_genetic_diseases|not_specified|Myofibrillar_myopathy_3": 1,
    "not_provided|Myofibrillar_myopathy_3|Inborn_genetic_diseases": 2,
    "Myofibrillar_myopathy_3|not_specified": 4,
    "MYOT-related_disorder|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|not_provided|not_specified|Myofibrillar_myopathy_3": 1,
    "not_specified|Myofibrillar_myopathy_3": 3,
    "MYOT-related_disorder|Myofibrillar_myopathy_3": 1,
    "Myofibrillar_myopathy_3|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|MYOT-related_disorder|Myofibrillar_myopathy_3": 1,
    "not_specified|Inborn_genetic_diseases|Myofibrillar_myopathy_3": 1,
    "not_specified|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_myopathy_3|not_provided": 1,
    "MYOT-related_disorder": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|MYOT-related_disorder|Myofibrillar_Myopathy|_Dominant|not_provided|not_specified|Myofibrillar_myopathy_3": 1,
    "Myofibrillar_Myopathy|_Dominant|Limb-Girdle_Muscular_Dystrophy|_Dominant|not_specified|not_provided|Myofibrillar_myopathy_3": 1,
    "Muscle_weakness": 7,
    "Inborn_genetic_diseases|not_provided|Myofibrillar_myopathy_3": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|not_specified|Myofibrillar_myopathy_3": 1,
    "Inborn_genetic_diseases|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|not_provided|Myofibrillar_myopathy_3": 1,
    "not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|Myofibrillar_myopathy_3": 1,
    "Myofibrillar_myopathy_3|not_specified|not_provided": 2,
    "Myofibrillar_myopathy_3|MYOT-related_disorder|Limb-Girdle_Muscular_Dystrophy|_Dominant|not_provided|Myofibrillar_Myopathy|_Dominant|not_specified": 1,
    "not_provided|Myofibrillar_myopathy_3|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Myofibrillar_myopathy_3|not_specified": 1,
    "not_specified|MYOT-related_disorder|Myofibrillar_myopathy_3|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Myofibrillar_myopathy_3|Cardiomyopathy": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_myopathy_3|not_provided|Myofibrillar_Myopathy|_Dominant|Inborn_genetic_diseases": 1,
    "Myofibrillar_myopathy_3|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant": 1,
    "Hypospadias": 4,
    "Congenital_fibrosis_of_extraocular_muscles": 9,
    "WNT8A-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_48|_without_situs_inversus": 4,
    "not_provided|Cardiomyopathy|_familial_restrictive|_6": 1,
    "not_provided|KIF20A-related_disorder": 1,
    "KDM3B-related_disorder": 31,
    "Diets-Jongmans_syndrome": 43,
    "not_provided|Diets-Jongmans_syndrome|KDM3B-related_disorder": 2,
    "not_provided|Diets-Jongmans_syndrome": 2,
    "KDM3B-related_disorder|not_provided": 5,
    "KDM3B-related_disorder|Diets-Jongmans_syndrome": 1,
    "not_provided|KDM3B-related_disorder": 7,
    "Inborn_genetic_diseases|KDM3B-related_disorder": 2,
    "Inborn_genetic_diseases|KDM3B-related_disorder|not_provided": 1,
    "KDM3B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KDM3B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "KDM3B-related_disorder|Inborn_genetic_diseases": 2,
    "Diets-Jongmans_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|KDM3B-related_disorder": 1,
    "Rare_genetic_intellectual_disability|Rare_genetic_epilepsy": 1,
    "not_provided|KDM3B-related_disorder|Neurodevelopmental_delay": 1,
    "See_cases|Diets-Jongmans_syndrome": 1,
    "Diets-Jongmans_syndrome|not_provided": 2,
    "Diets-Jongmans_syndrome|Developmental_disorder|not_provided": 1,
    "REEP2-related_disorder": 3,
    "Hereditary_spastic_paraplegia_72": 90,
    "Spastic_paraplegia_72b|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_72": 2,
    "Hereditary_spastic_paraplegia_72|REEP2-related_disorder": 2,
    "Hereditary_spastic_paraplegia_72|Spastic_paraplegia_72b|_autosomal_recessive": 1,
    "Hereditary_spastic_paraplegia_72|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_72": 1,
    "Hereditary_spastic_paraplegia_72|not_specified": 1,
    "Hereditary_spastic_paraplegia_72|not_provided": 1,
    "Hereditary_spastic_paraplegia_72|Hereditary_spastic_paraplegia_5A": 1,
    "not_provided|Hereditary_spastic_paraplegia_72": 1,
    "Even-plus_syndrome|Autosomal_dominant_sideroblastic_anemia": 1,
    "not_provided|Even-plus_syndrome": 1,
    "HSPA9-related_disorder": 4,
    "not_provided|HSPA9-related_disorder": 1,
    "HSPA9-related_disorder|not_provided": 3,
    "Autosomal_dominant_sideroblastic_anemia|not_provided": 1,
    "Inborn_genetic_diseases|Even-plus_syndrome|Autosomal_dominant_sideroblastic_anemia": 2,
    "HSPA9-related_disorder|Autosomal_dominant_sideroblastic_anemia|Even-plus_syndrome|not_provided": 1,
    "Even-plus_syndrome": 3,
    "not_provided|Even-plus_syndrome|Autosomal_dominant_sideroblastic_anemia": 1,
    "Autosomal_dominant_sideroblastic_anemia": 2,
    "Autosomal_dominant_sideroblastic_anemia|Even-plus_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma": 1660,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 568,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 78,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 539,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 61,
    "Patterned_macular_dystrophy_2|not_provided": 5,
    "not_provided|Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome": 16,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Retinal_dystrophy": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 81,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 99,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 108,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CTNNA1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Patterned_macular_dystrophy_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Patterned_macular_dystrophy_2|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 50,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 101,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 69,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|not_provided": 12,
    "Polyposis_syndrome|_hereditary_mixed|_1": 10,
    "CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 3,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Patterned_macular_dystrophy_2|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Patterned_macular_dystrophy_2|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Patterned_macular_dystrophy_2": 1,
    "Patterned_macular_dystrophy_2": 9,
    "CTNNA1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "not_provided|Patterned_macular_dystrophy_2|Polyposis_syndrome|_hereditary_mixed|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2": 14,
    "not_provided|Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder": 1,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Patterned_macular_dystrophy_2": 10,
    "not_provided|CTNNA1-related_disorder": 4,
    "Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CTNNA1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Patterned_macular_dystrophy_2|not_provided|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2": 1,
    "CTNNA1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|Patterned_macular_dystrophy_2|not_provided": 1,
    "CTNNA1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "not_provided|Patterned_macular_dystrophy_2": 4,
    "Patterned_macular_dystrophy_2|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2|not_provided": 5,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Patterned_macular_dystrophy_2|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Patterned_macular_dystrophy_2": 2,
    "Patterned_macular_dystrophy_2|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "CTNNA1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Retinal_dystrophy|not_provided": 3,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Patterned_macular_dystrophy_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|Patterned_macular_dystrophy_2": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Patterned_macular_dystrophy_2|CTNNA1-related_disorder": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|Patterned_macular_dystrophy_2|not_provided": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CTNNA1-related_disorder": 3,
    "CTNNA1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "not_provided|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|not_provided|Retinal_dystrophy": 2,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 6,
    "Hereditary_nonpolyposis_colon_cancer|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2|not_specified": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder|Hereditary_nonpolyposis_colon_cancer|Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Retinal_dystrophy|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided": 3,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Patterned_macular_dystrophy_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|not_provided|Patterned_macular_dystrophy_2": 1,
    "not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified|Patterned_macular_dystrophy_2": 1,
    "not_specified|Hereditary_nonpolyposis_colon_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|Polyposis_syndrome|_hereditary_mixed|_1": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Patterned_macular_dystrophy_2": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder": 3,
    "Patterned_macular_dystrophy_2|CTNNA1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|CTNNA1-related_disorder": 1,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified": 1,
    "Patterned_macular_dystrophy_2|Hereditary_nonpolyposis_colon_cancer|not_provided|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|CTNNA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Patterned_macular_dystrophy_2|Hereditary_diffuse_gastric_adenocarcinoma|Retinal_dystrophy|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "CTNNA1-related_disorder": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|CTNNA1-associated_FEVR|not_provided|Patterned_macular_dystrophy_2": 1,
    "Patterned_macular_dystrophy_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Patterned_macular_dystrophy_2|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CTNNA1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified|Hereditary_nonpolyposis_colon_cancer": 1,
    "CTNNA1-related_disorder|Patterned_macular_dystrophy_2|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Patterned_macular_dystrophy_2|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Patterned_macular_dystrophy_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CTNNA1-related_disorder": 1,
    "CTNNA1-related_disorder|not_provided|Patterned_macular_dystrophy_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Polyposis_syndrome|_hereditary_mixed|_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Patterned_macular_dystrophy_2|not_provided|Hereditary_cancer-predisposing_syndrome|CTNNA1-related_disorder": 1,
    "Marinesco-Sj\u00f6gren_syndrome|not_provided|SIL1-related_disorder|not_specified": 1,
    "Marinesco-Sj\u00f6gren_syndrome|SIL1-related_disorder": 2,
    "not_provided|Marinesco-Sj\u00f6gren_syndrome": 21,
    "SIL1-related_disorder": 3,
    "Marinesco-Sj\u00f6gren_syndrome|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|Marinesco-Sj\u00f6gren_syndrome": 13,
    "Marinesco-Sj\u00f6gren_syndrome|not_provided": 12,
    "not_provided|not_specified|Marinesco-Sj\u00f6gren_syndrome|SIL1-related_disorder": 1,
    "not_specified|SIL1-related_disorder|Marinesco-Sj\u00f6gren_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Marinesco-Sj\u00f6gren_syndrome": 2,
    "SIL1-related_disorder|not_provided|Marinesco-Sj\u00f6gren_syndrome": 2,
    "Marinesco-Sj\u00f6gren_syndrome|not_specified": 5,
    "Marinesco-Sj\u00f6gren_syndrome|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Marinesco-Sj\u00f6gren_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Marinesco-Sj\u00f6gren_syndrome": 5,
    "not_provided|Marinesco-Sj\u00f6gren_syndrome|See_cases": 1,
    "SIL1-related_disorder|Marinesco-Sj\u00f6gren_syndrome": 2,
    "not_provided|Marinesco-Sj\u00f6gren_syndrome|not_specified": 4,
    "Marinesco-Sj\u00f6gren_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Marinesco-Sj\u00f6gren_syndrome": 4,
    "Inborn_genetic_diseases|Marinesco-Sj\u00f6gren_syndrome|not_provided": 1,
    "not_specified|not_provided|Marinesco-Sj\u00f6gren_syndrome": 3,
    "Inborn_genetic_diseases|not_specified|Marinesco-Sj\u00f6gren_syndrome": 1,
    "not_specified|Marinesco-Sj\u00f6gren_syndrome|not_provided": 1,
    "SIL1-related_disorder|not_specified|not_provided|Marinesco-Sj\u00f6gren_syndrome": 1,
    "not_specified|X-linked_intellectual_disability-short_stature-overweight_syndrome|not_provided|Marinesco-Sj\u00f6gren_syndrome": 1,
    "not_provided|Marinesco-Sj\u00f6gren_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Marinesco-Sj\u00f6gren_syndrome|SIL1-related_disorder": 1,
    "Marinesco-Sj\u00f6gren_syndrome|not_specified|not_provided": 1,
    "Marinesco-Sj\u00f6gren_syndrome|SIL1-related_disorder|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_21": 427,
    "not_specified|Amyotrophic_lateral_sclerosis_type_21|Distal_myopathy_with_vocal_cord_weakness": 1,
    "MATR3-related_disorder": 20,
    "not_provided|MATR3-related_disorder": 1,
    "Distal_myopathy|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_21": 11,
    "not_specified|Amyotrophic_lateral_sclerosis_type_21|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_21|Inborn_genetic_diseases": 12,
    "Amyotrophic_lateral_sclerosis_type_21|not_provided": 5,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_21": 12,
    "not_provided|MATR3-related_disorder|Amyotrophic_lateral_sclerosis_type_21": 3,
    "MATR3-related_disorder|Amyotrophic_lateral_sclerosis_type_21": 7,
    "Neurodegeneration|not_provided|Amyotrophic_lateral_sclerosis_type_21": 1,
    "Amyotrophic_lateral_sclerosis_type_21|MATR3-related_disorder": 11,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_21": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_21": 1,
    "Amyotrophic_lateral_sclerosis_type_21|not_specified": 1,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_21": 1,
    "Amyotrophic_lateral_sclerosis_type_21|MATR3-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_21|MATR3-related_disorder|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_21|Distal_myopathy_with_vocal_cord_weakness": 1,
    "MATR3-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_21": 3,
    "MATR3-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_21": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_21|MATR3-related_disorder": 1,
    "STING-associated_vasculopathy_with_onset_in_infancy": 255,
    "STING-associated_vasculopathy_with_onset_in_infancy|Inborn_genetic_diseases": 11,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy": 2,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy|not_provided": 1,
    "Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy|not_provided": 1,
    "STING-associated_vasculopathy_with_onset_in_infancy|not_provided": 5,
    "STING-associated_vasculopathy_with_onset_in_infancy|Autoinflammatory_syndrome": 4,
    "STING-associated_vasculopathy_with_onset_in_infancy|Inborn_genetic_diseases|not_provided": 1,
    "Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy": 8,
    "Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy|not_specified": 1,
    "not_provided|Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy|not_specified": 2,
    "Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy": 10,
    "Autoinflammatory_syndrome|not_provided|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "STING-associated_vasculopathy_with_onset_in_infancy|not_specified": 1,
    "Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome": 2,
    "not_provided|STING1-related_disorder|Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "not_provided|STING-associated_vasculopathy_with_onset_in_infancy": 3,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "not_provided|not_specified|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "not_provided|STING-associated_vasculopathy_with_onset_in_infancy|not_specified": 1,
    "Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy|not_provided|not_specified": 1,
    "STING1-related_disorder|STING-associated_vasculopathy_with_onset_in_infancy|not_provided|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy|Inborn_genetic_diseases|STING1-related_disorder|not_provided": 1,
    "STING-associated_vasculopathy_with_onset_in_infancy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy|not_provided": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy|not_provided|STING1-related_disorder": 1,
    "Inborn_genetic_diseases|STING-associated_vasculopathy_with_onset_in_infancy|Autoinflammatory_syndrome|not_provided": 1,
    "STING-associated_vasculopathy_with_onset_in_infancy|STING1-related_disorder": 1,
    "not_specified|not_provided|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases|STING1-related_disorder|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "STING-associated_vasculopathy_with_onset_in_infancy|Autoinflammatory_syndrome|not_provided": 1,
    "STING1-related_disorder|Autoinflammatory_syndrome|STING-associated_vasculopathy_with_onset_in_infancy": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 332,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided": 21,
    "not_provided|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 16,
    "PURA-related_disorder": 7,
    "Inborn_genetic_diseases|Intellectual_disability|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome_due_to_a_point_mutation": 4,
    "Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 11,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_specified": 5,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_specified|not_provided": 1,
    "Epileptic_encephalopathy|not_provided": 146,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases": 8,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "PURA_Syndrome|not_provided": 1,
    "PURA-related_disorder|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "not_specified|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases|not_specified|not_provided|PURA-related_disorder": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|PURA-related_disorder|Inborn_genetic_diseases": 1,
    "PURA-related_disorder|Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided": 1,
    "not_provided|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|PURA-related_disorder": 1,
    "not_provided|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome_due_to_a_point_mutation|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Intellectual_disability": 1,
    "not_specified|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 2,
    "PURA_Syndrome|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "Inborn_genetic_diseases|PURA-related_disorder|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "Global_developmental_delay|Intellectual_disability|Neonatal_hypotonia|Delayed_speech_and_language_development|Seizure": 1,
    "Delayed_speech_and_language_development|Seizure|Intellectual_disability|Neonatal_hypotonia|Global_developmental_delay|not_provided|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided|Global_developmental_delay|Delayed_speech_and_language_development|Seizure|Intellectual_disability|Neonatal_hypotonia": 3,
    "Delayed_speech_and_language_development|Seizure|Intellectual_disability|Neonatal_hypotonia|Global_developmental_delay|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 2,
    "Delayed_speech_and_language_development|Intellectual_disability|Neonatal_hypotonia|Global_developmental_delay|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|PURA-related_disorder": 1,
    "not_provided|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|PURA-related_disorder|Abnormality_of_the_nervous_system|Global_developmental_delay|Intellectual_disability|Neonatal_hypotonia|Delayed_speech_and_language_development|Seizure": 1,
    "PURA_Syndrome": 1,
    "Intellectual_disability|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided|PURA-related_disorder": 1,
    "Global_developmental_delay|Intellectual_disability|Neonatal_hypotonia|Delayed_speech_and_language_development": 1,
    "Global_developmental_delay-visual_anomalies-progressive_cerebellar_atrophy-truncal_hypotonia_syndrome": 1,
    "PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome_due_to_a_point_mutation": 1,
    "PURA-related_disorder|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome_due_to_a_point_mutation|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided|PURA-related_disorder|not_specified": 1,
    "Limb_dystonia|Generalized_hypotonia|Apnea|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "Inborn_genetic_diseases|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|Intellectual_disability|not_provided": 1,
    "PURA-related_disorder|Inborn_genetic_diseases|PURA_Syndrome|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome|not_provided": 1,
    "See_cases|PURA_Syndrome|PURA-related_severe_neonatal_hypotonia-seizures-encephalopathy_syndrome": 1,
    "not_provided|Global_developmental_delay|Intellectual_disability|Neonatal_hypotonia|Delayed_speech_and_language_development|Seizure": 1,
    "not_provided|SRA1-related_disorder": 1,
    "not_specified|not_provided|SRA1-related_disorder": 1,
    "SRA1-related_disorder|not_provided": 5,
    "Hypogonadism_with_anosmia": 6,
    "SRA1-related_disorder": 4,
    "CD14-related_disorder": 1,
    "NDUFA2-related_disorder": 1,
    "not_provided|NDUFA2-related_disorder|not_specified": 2,
    "Cystic_Leukoencephalopathy|Mitochondrial_complex_I_deficiency|_nuclear_type_13|not_provided": 1,
    "not_specified|NDUFA2-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_13": 4,
    "Cystic_Leukoencephalopathy|Mitochondrial_complex_I_deficiency|_nuclear_type_13": 1,
    "NDUFA2-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Leigh_syndrome": 2,
    "NDUFA2-related_disorder|not_specified|not_provided": 1,
    "HARS1-related_multi-system_ataxia_syndrome": 1,
    "Usher_syndrome_type_3B": 395,
    "not_provided|Usher_syndrome_type_3B|not_specified": 10,
    "not_specified|Usher_syndrome_type_3B": 23,
    "not_specified|Usher_syndrome_type_3B|not_provided": 4,
    "Usher_syndrome_type_3B|not_specified": 30,
    "Pes_cavus": 1,
    "HARS1-related_disorder": 1,
    "Usher_syndrome_type_3B|Retinal_dystrophy|not_provided|HARS1-related_disorder": 1,
    "Usher_syndrome_type_3B|not_specified|not_provided": 5,
    "not_provided|Usher_syndrome_type_3B": 27,
    "Usher_syndrome_type_3B|not_provided": 14,
    "not_specified|not_provided|Usher_syndrome_type_3B": 5,
    "Cerebellar_ataxia|Microcephaly|Intellectual_disability|Dysarthria|Pes_planus|Motor_delay|Scoliosis|Joint_laxity|Hammertoe|Distal_muscle_weakness|Urinary_urgency|Peripheral_neuropathy|Usher_syndrome_type_3B|HARS1-related_disorder|Spastic_ataxia": 1,
    "Usher_syndrome_type_3B|not_provided|not_specified": 4,
    "not_specified|Usher_syndrome_type_3B|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Usher_syndrome_type_3B": 3,
    "Charcot-Marie-Tooth_disease|Usher_syndrome_type_3B|not_provided|Retinal_dystrophy": 1,
    "not_specified|Usher_syndrome_type_3B|not_provided|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W|Usher_syndrome_type_3": 1,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W": 6,
    "Usher_syndrome_type_3B|not_specified|not_provided|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W": 1,
    "Usher_syndrome_type_3B|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W": 2,
    "Usher_syndrome_type_3B|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W|not_provided": 2,
    "not_provided|Usher_syndrome_type_3B|HARS1-related_multi-system_ataxia_syndrome": 1,
    "Cerebellar_ataxia|Microcephaly|Intellectual_disability|Dysarthria|Pes_planus|Motor_delay|Scoliosis|Joint_laxity|Hammertoe|Distal_muscle_weakness|Urinary_urgency|Spastic_ataxia": 1,
    "Usher_syndrome_type_3B|HARS1-related_disorder": 2,
    "Spastic_ataxia|Intellectual_disability|Choreoathetosis|Peripheral_neuropathy|Cerebellar_atrophy|Dysmetria|Tremor|Oculomotor_apraxia|Dysarthria|Nystagmus": 2,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W|not_specified|Usher_syndrome_type_3B": 1,
    "not_provided|Usher_syndrome_type_3B|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W|not_specified": 1,
    "Retinitis_pigmentosa-deafness_syndrome": 6,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W|not_provided": 1,
    "Usher_syndrome_type_3B|not_provided|HARS1-related_disorder": 1,
    "not_provided|Usher_syndrome_type_3B|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2W": 1,
    "HARS1-related_disorder|not_specified|not_provided|Usher_syndrome_type_3B": 1,
    "not_specified|not_provided|Spastic_ataxia|Usher_syndrome_type_3B": 1,
    "Usher_syndrome_type_3B|Inborn_genetic_diseases": 1,
    "HARS1-related_disorder|Usher_syndrome_type_3B|not_provided": 1,
    "HARS1-related_disorder|not_provided|Usher_syndrome_type_3B|not_specified": 1,
    "Usher_syndrome_type_3B|HARS1-related_disorder|not_specified": 1,
    "HARS2-related_disorder": 3,
    "not_provided|Perrault_syndrome_2": 5,
    "Perrault_syndrome_2": 15,
    "Perrault_syndrome_2|not_provided": 5,
    "HARS2-related_disorder|not_specified|not_provided|Perrault_syndrome_2": 2,
    "not_provided|Sensorineural_hearing_loss_disorder|HARS2-related_disorder": 1,
    "not_specified|not_provided|Perrault_syndrome_2": 1,
    "not_provided|Perrault_syndrome_2|Perrault_syndrome": 1,
    "HARS2-related_disorder|not_provided": 4,
    "not_specified|Perrault_syndrome_2|not_provided": 1,
    "Perrault_syndrome_2|Perrault_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Perrault_syndrome_2": 1,
    "Sensorineural_hearing_loss_disorder|Perrault_syndrome|not_provided": 1,
    "PCDHA2-related_disorder": 2,
    "PCDHA3-related_disorder": 19,
    "not_specified|PCDHA3-related_disorder": 1,
    "not_provided|PCDHA3-related_disorder": 1,
    "PCDHA3-related_disorder|not_provided": 1,
    "PCDHA9-related_disorder": 36,
    "not_provided|PCDHA9-related_disorder": 4,
    "PCDHA9-related_disorder|not_specified": 1,
    "PCDHA9-related_disorder|not_provided": 2,
    "Thrombocytosis": 2,
    "PCDHA12-related_condition": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|not_provided": 1,
    "PCDHA13-related_disorder": 2,
    "Microcephaly|Intellectual_disability|Seizure|Epilepsy|not_provided": 1,
    "Neurodevelopmental_disorder_with_poor_growth_and_skeletal_anomalies": 8,
    "Neurodevelopmental_disorder_with_poor_growth_and_skeletal_anomalies|not_provided": 1,
    "PCDHGC4-related_disorder": 1,
    "Nonsyndromic_Hearing_Loss|_Mixed|not_provided": 3,
    "Nonsyndromic_Hearing_Loss|_Mixed": 24,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1": 63,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided": 20,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 725,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 473,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 6,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|Inborn_genetic_diseases": 10,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_specified": 11,
    "DIAPH1-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 10,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified": 3,
    "Macrothrombocytopenia": 32,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Inborn_genetic_diseases|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Rare_genetic_deafness|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided": 1,
    "Macrothrombocytopenia|Hearing_impairment": 1,
    "DIAPH1-related_disorder": 8,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "DIAPH1-related_disorder|not_provided|not_specified|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 2,
    "DIAPH1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 2,
    "not_specified|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 4,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 9,
    "not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 19,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 22,
    "Neonatal_seizure": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases": 21,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 3,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided": 10,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_specified|not_provided": 3,
    "not_provided|Beta-D-mannosidosis|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|DIAPH1-related_disorder": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided|Hearing_impairment": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_specified": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified|not_provided": 4,
    "not_provided|DIAPH1-related_disorder": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Deafness|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided": 2,
    "See_cases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided|not_specified": 1,
    "DIAPH1-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|Inborn_genetic_diseases|not_specified": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder|not_specified": 1,
    "not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 12,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder|Intellectual_disability|not_provided": 1,
    "not_specified|not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 2,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 4,
    "Inborn_genetic_diseases|not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 4,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided": 2,
    "not_provided|DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Global_developmental_delay|Microcephaly|Epilepsy|Failure_to_thrive": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided|DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 1,
    "DIAPH1-related_disorder|Inborn_genetic_diseases|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|Hearing_impairment": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Inborn_genetic_diseases|DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "DIAPH1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided": 1,
    "DIAPH1-related_sensorineural_hearing_loss-thrombocytopenia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided|DIAPH1-related_disorder|Inborn_genetic_diseases": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|not_provided|not_specified": 2,
    "not_provided|DIAPH1-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Nonsyndromic_Hearing_Loss|_Mixed|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified|not_provided": 2,
    "not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified": 1,
    "DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|DIAPH1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Microcephaly|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Nonsyndromic_Hearing_Loss|_Mixed": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Vascular_dementia|not_provided": 1,
    "not_specified|DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided|not_specified|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|not_provided|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_1|DIAPH1-related_disorder|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_1|Progressive_microcephaly-seizures-cortical_blindness-developmental_delay_syndrome|DIAPH1-related_disorder|not_specified": 1,
    "DIAPH1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_1|not_specified": 1,
    "HDAC3-related_disorder": 1,
    "not_provided|Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|PCDH12-related_disorder": 2,
    "not_provided|PCDH12-related_disorder": 7,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_1": 16,
    "Inborn_genetic_diseases|Diencephalic-mesencephalic_junction_dysplasia_syndrome_1": 1,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|Inborn_genetic_diseases|not_provided": 4,
    "PCDH12-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|not_provided": 9,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|Diencephalic-mesencephalic_junction_dysplasia": 2,
    "not_provided|Diencephalic-mesencephalic_junction_dysplasia_syndrome_1": 4,
    "PCDH12-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|not_provided": 1,
    "not_provided|PCDH12-related_disorder|Inborn_genetic_diseases": 1,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Exudative_retinopathy|Dystonic_disorder|Abnormal_facial_shape|Cerebellar_ataxia": 1,
    "Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|Inborn_genetic_diseases": 1,
    "PCDH12-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Diencephalic-mesencephalic_junction_dysplasia_syndrome_1|not_provided": 1,
    "not_provided|Diencephalic-mesencephalic_junction_dysplasia": 1,
    "Diencephalic-mesencephalic_junction_dysplasia|Disorder_of_development_or_morphogenesis": 1,
    "Diencephalic-mesencephalic_junction_dysplasia": 1,
    "Diencephalic-mesencephalic_junction_dysplasia|not_provided|Diencephalic-mesencephalic_junction_dysplasia_syndrome_1": 1,
    "not_provided|Hypogonadotropic_hypogonadism_17_with_or_without_anosmia": 1,
    "SPRY4-related_disorder": 8,
    "SPRY4-related_disorder|not_provided": 2,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_17_with_or_without_anosmia": 1,
    "not_provided|Amenorrhea|Hypogonadotropic_hypogonadism_17_with_or_without_anosmia|not_specified": 1,
    "not_specified|Hypogonadism_with_anosmia": 1,
    "not_specified|Hypogonadotropic_hypogonadism_17_with_or_without_anosmia|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "SPRY4-related_disorder|not_provided|Hypogonadotropic_hypogonadism_17_with_or_without_anosmia": 1,
    "not_provided|SPRY4-related_disorder|not_specified": 1,
    "Hypogonadotropic_hypogonadism_17_with_or_without_anosmia": 2,
    "not_provided|SPRY4-related_disorder": 3,
    "ARHGAP26-related_disorder": 11,
    "not_specified|Juvenile_myelomonocytic_leukemia": 1,
    "Glucocorticoid_resistance": 173,
    "not_provided|Glucocorticoid_resistance": 9,
    "Glucocorticoid_resistance|not_provided": 11,
    "GLUCOCORTICOID_RESISTANCE|_CELLULAR": 1,
    "Glucocorticoid_resistance|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Glucocorticoid_resistance": 4,
    "NR3C1-related_disorder|Glucocorticoid_resistance|not_provided": 2,
    "Deficiency_of_galactokinase": 457,
    "GLUCOCORTICOID_RESISTANCE|_ATYPICAL": 1,
    "Inborn_genetic_diseases|NR3C1-related_disorder": 1,
    "NR3C1_POLYMORPHISM|Glucocorticoid_resistance|not_provided": 1,
    "Glucocorticoid_resistance|not_provided|NR3C1-related_disorder": 2,
    "not_provided|Glucocorticoid_resistance|not_specified": 1,
    "not_provided|Glucocorticoid_resistance|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Glucocorticoid_resistance": 1,
    "Glucocorticoid_resistance|GLUCOCORTICOID_RESISTANCE|_MILD": 1,
    "NR3C1-related_disorder|not_provided|Glucocorticoid_resistance": 1,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome_2": 6,
    "GRXCR2-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_101": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_101|not_specified|not_provided": 1,
    "GRXCR2-related_disorder|not_provided": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_101": 1,
    "not_provided|GRXCR2-related_disorder": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_101|not_specified": 1,
    "not_specified|LARS1-related_disorder|not_provided": 1,
    "Infantile_liver_failure_syndrome_1": 11,
    "LARS1-related_disorder|Infantile_liver_failure_syndrome_1|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "not_specified|Infantile_liver_failure_syndrome_1": 3,
    "not_provided|LARS1-related_disorder": 2,
    "not_provided|LARS1-related_disorder|not_specified": 2,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided|Infantile_liver_failure_syndrome_1": 1,
    "LARS1-related_disorder": 5,
    "LARS1-related_disorder|not_provided|not_specified": 2,
    "not_provided|Infantile_liver_failure_syndrome_1|not_specified": 1,
    "not_specified|Sensorineural_hearing_loss_disorder|Global_developmental_delay|Generalized-onset_seizure|Normochromic_microcytic_anemia|not_provided": 1,
    "LARS1-related_disorder|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Infantile_liver_failure_syndrome_1": 1,
    "Infantile_liver_failure_syndrome_1|not_specified|not_provided": 1,
    "not_specified|Infantile_liver_failure_syndrome_1|not_provided": 1,
    "not_specified|not_provided|Infantile_liver_failure_syndrome_1": 1,
    "RBM27-related_disorder": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_15": 48,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_15": 8,
    "POU4F3-related_disorder|Inborn_genetic_diseases": 1,
    "POU4F3-related_disorder": 5,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_15": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_15|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Hearing_impairment|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "not_specified|POU4F3-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_15|Inborn_genetic_diseases": 1,
    "POU4F3-related_disorder|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_sensorineural_hearing_loss": 1,
    "POU4F3-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "POU4F3-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_15|Congenital_sensorineural_hearing_impairment": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|not_provided": 5,
    "POU4F3-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_15": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_15|POU4F3-related_disorder|not_specified|not_provided": 1,
    "Essential_tremor|not_provided": 2,
    "Spinocerebellar_ataxia_type_12": 4,
    "not_provided|Spinocerebellar_ataxia_type_12": 1,
    "PPP2R2B-related_disorder": 6,
    "not_provided|PPP2R2B-related_disorder": 1,
    "PPP2R2B-related_disorder|not_provided": 2,
    "PPP2R2B-related_disorder|not_specified": 1,
    "not_specified|PPP2R2B-related_disorder": 1,
    "not_specified|Hereditary_pancreatitis|not_provided": 4,
    "Hereditary_pancreatitis|not_provided|not_specified": 7,
    "Hereditary_pancreatitis|SPINK1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Hereditary_pancreatitis|Tropical_pancreatitis": 1,
    "not_provided|Tropical_pancreatitis|Hereditary_pancreatitis|SPINK1-related_disorder|not_specified": 1,
    "SPINK1-related_disorder|Diabetes_mellitus|Chronic_pancreatitis|not_provided|Hereditary_pancreatitis|Tropical_pancreatitis": 1,
    "not_provided|Tropical_pancreatitis|Hereditary_pancreatitis|not_specified": 1,
    "Hereditary_pancreatitis|Tropical_pancreatitis": 3,
    "SPINK1-related_disorder|Hereditary_pancreatitis": 1,
    "SPINK1-related_disorder|not_provided|not_specified|Tropical_pancreatitis|Hereditary_pancreatitis": 1,
    "not_provided|Hereditary_pancreatitis|Tropical_pancreatitis": 2,
    "Pancreatitis|not_provided|Tropical_pancreatitis|Hereditary_pancreatitis|Finnish_congenital_nephrotic_syndrome|Pancreatitis|_chronic|_susceptibility_to": 1,
    "not_provided|not_specified|Hereditary_pancreatitis": 6,
    "not_specified|Tropical_pancreatitis|Hereditary_pancreatitis": 1,
    "not_provided|Hereditary_pancreatitis|SPINK1-related_disorder|not_specified": 1,
    "Pancreatitis|_chronic|_susceptibility_to": 1,
    "Hereditary_pancreatitis|Tropical_pancreatitis|not_provided": 1,
    "Tropical_pancreatitis|Hereditary_pancreatitis|not_provided|SPINK1-related_disorder": 2,
    "Tropical_pancreatitis": 1,
    "SPINK1-related_disorder|not_provided|Hereditary_pancreatitis|Tropical_pancreatitis": 1,
    "Ichthyosis_linearis_circumflexa|not_provided": 15,
    "not_provided|Netherton_syndrome": 10,
    "Netherton_syndrome|not_provided": 10,
    "Netherton_syndrome": 116,
    "Ichthyosis_linearis_circumflexa": 482,
    "Ichthyosis_linearis_circumflexa|Inborn_genetic_diseases": 15,
    "Ichthyosis_linearis_circumflexa|Netherton_syndrome": 16,
    "Ichthyosis_linearis_circumflexa|not_provided|Netherton_syndrome": 7,
    "Netherton_syndrome|not_provided|not_specified": 3,
    "not_provided|Netherton_syndrome|Ichthyosis_linearis_circumflexa": 5,
    "SPINK5-related_disorder": 3,
    "not_specified|not_provided|Ichthyosis_linearis_circumflexa|Netherton_syndrome": 5,
    "Netherton_syndrome|not_specified|Ichthyosis_linearis_circumflexa|not_provided": 5,
    "Ichthyosis_linearis_circumflexa|Netherton_syndrome|not_provided": 2,
    "not_provided|Ichthyosis_linearis_circumflexa|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ichthyosis_linearis_circumflexa": 8,
    "Netherton_syndrome|Inborn_genetic_diseases": 14,
    "Netherton_syndrome|Ichthyosis_linearis_circumflexa|not_specified": 5,
    "Ichthyosis_linearis_circumflexa|Susceptibility_to_nonsyndromic_otitis_media": 1,
    "not_provided|Ichthyosis_linearis_circumflexa": 12,
    "Netherton_syndrome|not_provided|Susceptibility_to_nonsyndromic_otitis_media": 1,
    "SPINK5-related_disorder|Netherton_syndrome|Ichthyosis_linearis_circumflexa": 1,
    "Netherton_syndrome|Ichthyosis_linearis_circumflexa": 12,
    "SPINK5-related_disorder|Susceptibility_to_nonsyndromic_otitis_media|not_provided|Netherton_syndrome|Ichthyosis_linearis_circumflexa": 1,
    "Netherton_syndrome|not_specified": 2,
    "Netherton_syndrome|Ichthyosis_linearis_circumflexa|Inborn_genetic_diseases": 2,
    "not_specified|Ichthyosis_linearis_circumflexa|Netherton_syndrome|not_provided": 1,
    "Netherton_syndrome|not_specified|not_provided": 2,
    "Ichthyosis_linearis_circumflexa|not_provided|Netherton_syndrome|Increased_circulating_IgE_concentration|Erythroderma": 1,
    "Netherton_syndrome|Ichthyosis_linearis_circumflexa|not_specified|not_provided": 3,
    "not_provided|Ichthyosis_linearis_circumflexa|Netherton_syndrome": 3,
    "not_provided|Netherton_syndrome|Ichthyosis_linearis_circumflexa|not_specified": 4,
    "Inborn_genetic_diseases|Netherton_syndrome": 9,
    "Netherton_syndrome|not_provided|Ichthyosis_linearis_circumflexa": 3,
    "Ichthyosis_linearis_circumflexa|SPINK5-related_disorder": 2,
    "SPINK5-related_disorder|not_provided|Ichthyosis_linearis_circumflexa": 2,
    "Netherton_syndrome|SPINK5_POLYMORPHISM|Ichthyosis_linearis_circumflexa|not_provided|not_specified": 1,
    "not_specified|Ichthyosis_linearis_circumflexa": 2,
    "not_provided|Ichthyosis_linearis_circumflexa|Netherton_syndrome|not_specified": 2,
    "not_specified|not_provided|Netherton_syndrome|Ichthyosis_linearis_circumflexa": 1,
    "Susceptibility_to_nonsyndromic_otitis_media|Netherton_syndrome": 1,
    "Ichthyosis_linearis_circumflexa|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Ichthyosis_linearis_circumflexa|Netherton_syndrome": 5,
    "Erythroderma|Increased_circulating_IgE_concentration|Ichthyosis_linearis_circumflexa|Netherton_syndrome|not_provided": 1,
    "Netherton_syndrome|SPINK5-related_disorder|Ichthyosis_linearis_circumflexa": 1,
    "SPINK5-related_disorder|Netherton_syndrome|not_provided|Ichthyosis_linearis_circumflexa": 1,
    "Netherton_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Ichthyosis_linearis_circumflexa|SPINK5-related_disorder|not_specified": 1,
    "SPINK5-related_disorder|Netherton_syndrome|Ichthyosis_linearis_circumflexa|not_provided": 1,
    "Otitis_media|_susceptibility_to|not_provided|Susceptibility_to_nonsyndromic_otitis_media|Ichthyosis_linearis_circumflexa": 1,
    "SPINK5-related_disorder|Ichthyosis_linearis_circumflexa": 1,
    "SPINK5-related_disorder|Netherton_syndrome": 1,
    "Inborn_genetic_diseases|Netherton_syndrome|Ichthyosis_linearis_circumflexa": 1,
    "Ichthyosis_linearis_circumflexa|Netherton_syndrome|SPINK5-related_disorder|not_provided": 1,
    "Ichthyosis_linearis_circumflexa|not_provided|Netherton_syndrome|not_specified": 2,
    "Ichthyosis_linearis_circumflexa|Susceptibility_to_nonsyndromic_otitis_media|not_provided|Netherton_syndrome": 1,
    "not_specified|Netherton_syndrome|not_provided": 1,
    "not_provided|not_specified|Netherton_syndrome": 1,
    "Netherton_syndrome|Ichthyosis_linearis_circumflexa|not_provided": 2,
    "Ichthyosis_linearis_circumflexa|not_specified": 2,
    "Susceptibility_to_nonsyndromic_otitis_media": 6,
    "Ichthyosis_linearis_circumflexa|not_specified|Netherton_syndrome|not_provided": 1,
    "not_provided|Ichthyosis_linearis_circumflexa|not_specified": 1,
    "not_provided|Netherton_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Netherton_syndrome|SPINK5-related_disorder|Ichthyosis_linearis_circumflexa": 2,
    "Ichthyosis_linearis_circumflexa|not_provided|SPINK5-related_disorder|Netherton_syndrome": 1,
    "Ichthyosis_linearis_circumflexa|Netherton_syndrome|Inborn_genetic_diseases": 1,
    "SPINK5-related_disorder|Ichthyosis_linearis_circumflexa|Netherton_syndrome|Inborn_genetic_diseases": 1,
    "Ichthyosis_linearis_circumflexa|not_specified|Netherton_syndrome": 1,
    "Ichthyosis_linearis_circumflexa|not_specified|not_provided": 1,
    "not_provided|Netherton_syndrome|not_specified": 1,
    "Distal_hereditary_motor_neuropathy_type_2": 565,
    "Distal_hereditary_motor_neuropathy_type_2|not_specified": 22,
    "Neuronopathy|_distal_hereditary_motor|_type_2D|Distal_hereditary_motor_neuropathy_type_2|not_specified": 1,
    "Distal_hereditary_motor_neuropathy_type_2|FBXO38-related_disorder": 5,
    "not_provided|Distal_hereditary_motor_neuropathy_type_2": 11,
    "not_specified|Distal_hereditary_motor_neuropathy_type_2|FBXO38-related_disorder|not_provided": 1,
    "not_specified|Distal_hereditary_motor_neuropathy_type_2|Neuronopathy|_distal_hereditary_motor|_type_2D": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2D": 14,
    "Distal_hereditary_motor_neuropathy_type_2|not_provided": 11,
    "Neuronopathy|_distal_hereditary_motor|_type_2D|Distal_hereditary_motor_neuropathy_type_2": 4,
    "not_specified|Distal_hereditary_motor_neuropathy_type_2": 20,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2D": 1,
    "FBXO38-related_disorder|Distal_hereditary_motor_neuropathy_type_2": 6,
    "not_provided|not_specified|Distal_hereditary_motor_neuropathy_type_2": 2,
    "FBXO38-related_disorder": 4,
    "FBXO38-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_2D|Charcot-Marie-Tooth_disease|Distal_hereditary_motor_neuropathy_type_2|not_specified|not_provided": 1,
    "Distal_hereditary_motor_neuropathy_type_2|not_provided|Neuronopathy|_distal_hereditary_motor|_type_2D": 3,
    "Neuronopathy|_distal_hereditary_motor|_type_2D|not_specified|Distal_hereditary_motor_neuropathy_type_2|not_provided": 2,
    "Distal_hereditary_motor_neuropathy_type_2|Neuronopathy|_distal_hereditary_motor|_type_2D": 4,
    "Distal_hereditary_motor_neuropathy_type_2|not_provided|not_specified": 2,
    "Distal_hereditary_motor_neuropathy_type_2|FBXO38-related_disorder|Inborn_genetic_diseases": 1,
    "Distal_hereditary_motor_neuropathy_type_2|Distal_spinal_muscular_atrophy": 1,
    "Distal_hereditary_motor_neuropathy_type_2|not_specified|not_provided": 1,
    "Distal_hereditary_motor_neuropathy_type_2|not_specified|FBXO38-related_disorder|not_provided": 1,
    "not_specified|Distal_hereditary_motor_neuropathy_type_2|not_provided": 3,
    "Distal_hereditary_motor_neuropathy_type_2|FBXO38-related_disorder|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2D|not_specified": 1,
    "FBXO38-related_disorder|not_specified": 2,
    "not_specified|Distal_hereditary_motor_neuropathy_type_2|not_provided|FBXO38-related_disorder": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2D|Distal_hereditary_motor_neuropathy_type_2": 1,
    "Beta-2-adrenoreceptor_agonist|_reduced_response_to|not_provided": 2,
    "ADRB2-related_disorder": 3,
    "not_provided|RECLASSIFIED_-_ADRB2_POLYMORPHISM": 1,
    "salmeterol_response_-_Efficacy": 1,
    "ADRB2_POLYMORPHISM|not_provided": 1,
    "ADRB2-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Mononeuropathy_of_the_Median_Nerve": 41,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C": 244,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C": 35,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Mononeuropathy_of_the_Median_Nerve": 8,
    "Mononeuropathy_of_the_Median_Nerve|Charcot-Marie-Tooth_disease_type_4": 5,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 171,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided": 3,
    "Charcot-Marie-Tooth_disease_type_4C|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 8,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_provided": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided|Charcot-Marie-Tooth_disease_type_4C": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 4,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 9,
    "Charcot-Marie-Tooth_disease_type_4|not_provided": 114,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4|not_specified|Tip-toe_gait": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4": 89,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 5,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4C": 38,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_specified|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 264,
    "Tip-toe_gait|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided": 30,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 15,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4": 3,
    "SH3TC2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 3,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 63,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4": 4,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 187,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4": 3,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases": 4,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 19,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4C": 5,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 5,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 3,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C": 1,
    "Charcot-Marie-Tooth_disease|not_provided|SH3TC2-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 44,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases": 27,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|not_specified": 3,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Pes_cavus|Tip-toe_gait|limited_range_of_motion_of_the_upper_ankle|Delayed_speech_and_language_development|Inborn_genetic_diseases|SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 3,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Tip-toe_gait": 2,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 23,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 3,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 11,
    "not_provided|Charcot-Marie-Tooth_disease|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 5,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4": 20,
    "Autosomal_dominant_intermediate_Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Mononeuropathy_of_the_Median_Nerve|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified": 46,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 31,
    "not_provided|not_specified|SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder|not_specified": 1,
    "SH3TC2-related_disorder|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Tip-toe_gait": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4C": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified": 13,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 11,
    "not_provided|Inborn_genetic_diseases|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 3,
    "Charcot-Marie-Tooth_disease|SH3TC2-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease": 3,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 5,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|SH3TC2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease": 3,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C": 2,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided": 2,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided|Charcot-Marie-Tooth_disease_type_4C|Hereditary_motor_and_sensory_neuropathy|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C": 2,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 3,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Inborn_genetic_diseases": 11,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|SH3TC2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 3,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 3,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_specified|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 3,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases": 1,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|SH3TC2-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 3,
    "SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Hereditary_spastic_paraplegia|Tip-toe_gait": 1,
    "not_specified|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease": 7,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|SH3TC2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Hereditary_motor_neuron_disease|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4": 27,
    "Tip-toe_gait|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|SH3TC2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Tip-toe_gait|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "SH3TC2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4C|SH3TC2-related_disorder|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_1B|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "SH3TC2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_provided|Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "not_provided|SH3TC2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|not_specified|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C": 1,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 3,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|not_specified|Charcot-Marie-Tooth_disease_type_4C|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Tip-toe_gait|Hemihypertrophy|Short_lower_limbs|Upper_limb_undergrowth|Decreased_muscle_mass|Scoliosis|Congenital_contracture|Arthrogryposis_multiplex_congenita": 1,
    "not_specified|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases|Distal_spinal_muscular_atrophy|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild": 1,
    "Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease|not_provided|Tip-toe_gait|Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C": 1,
    "Hereditary_motor_and_sensory_neuropathy|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4C|not_specified": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|not_provided|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Inborn_genetic_diseases": 1,
    "Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4C|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4": 1,
    "SH3TC2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Susceptibility_to_mononeuropathy_of_the_median_nerve|_mild|Charcot-Marie-Tooth_disease_type_4C": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|not_specified": 2,
    "Charcot-Marie-Tooth_disease_type_4|SH3TC2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Mononeuropathy_of_the_Median_Nerve": 1,
    "MIR145-related_multisystemic_smooth_muscle_dysfunction": 1,
    "not_provided|PPARGC1B_polymorphism": 1,
    "not_provided|Retinitis_Pigmentosa|_Recessive": 7,
    "not_provided|Retinitis_pigmentosa_43": 9,
    "Retinitis_pigmentosa|PDE6A-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_43|not_provided": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_43|not_specified": 1,
    "Retinitis_pigmentosa_43|not_provided": 9,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Inborn_genetic_diseases": 3,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_43": 3,
    "Retinitis_pigmentosa_43": 20,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_43": 7,
    "Retinitis_pigmentosa_43|PDE6A-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_43|Retinal_dystrophy": 1,
    "PDE6A-related_disorder|not_provided": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_43|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_43|Retinal_dystrophy": 1,
    "not_provided|PDE6A-related_disorder": 3,
    "Retinitis_pigmentosa_43|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_43": 2,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_43": 2,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_43": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Retinal_dystrophy": 3,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_43": 3,
    "PDE6A-related_disorder|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_43": 1,
    "Retinitis_pigmentosa_43|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_43|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa": 7,
    "not_provided|Retinitis_pigmentosa|PDE6A-related_retinopathy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_43|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa|PDE6A-related_disorder": 1,
    "PDE6A-related_disorder": 1,
    "Retinal_dystrophy|not_provided|PDE6A-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_43|not_provided|Retinitis_pigmentosa": 1,
    "PDE6A-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_43|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_43": 2,
    "not_provided|Retinitis_pigmentosa_43|Retinitis_pigmentosa|Retinal_dystrophy|not_specified": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|PDE6A-related_disorder": 1,
    "PDE6A-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_43": 1,
    "not_provided|Retinitis_pigmentosa_43|Usher_syndrome|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa|PDE6A-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_43|Inborn_genetic_diseases|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|PDE6A-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_43": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB": 1,
    "Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 5,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia": 11,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II": 3,
    "Achondrogenesis|_type_IB": 56,
    "SLC26A2-related_disorder|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|not_provided|Sulfate_transporter-related_osteochondrodysplasia|3MC_syndrome_2": 1,
    "Multiple_epiphyseal_dysplasia_type_4": 23,
    "Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Atelosteogenesis_type_II": 2,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 188,
    "Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|not_provided": 2,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|not_provided": 1,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II": 11,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia": 71,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB": 12,
    "Diastrophic_dysplasia|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4": 14,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II": 23,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|SLC26A2-related_skeletal_dysplasia": 2,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 35,
    "not_provided|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB": 1,
    "Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II": 1,
    "Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB": 12,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II": 24,
    "Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB": 24,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia": 18,
    "Achondrogenesis|_type_IB|Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|not_provided": 1,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|not_provided": 2,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|not_specified|not_provided|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Diastrophic_dysplasia": 16,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 4,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 39,
    "Sulfate_transporter-related_osteochondrodysplasia|Inborn_genetic_diseases|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Achondrogenesis|_type_IB|Inborn_genetic_diseases": 1,
    "Atelosteogenesis_type_II": 2,
    "Diastrophic_dysplasia|not_provided|Connective_tissue_disorder": 1,
    "not_specified|Diastrophic_dysplasia": 1,
    "Diastrophic_dysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|not_specified": 1,
    "Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 3,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|not_provided": 2,
    "not_provided|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 2,
    "not_specified|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 1,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|not_provided|Sulfate_transporter-related_osteochondrodysplasia": 2,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|not_specified|Diastrophic_dysplasia|Atelosteogenesis_type_II": 1,
    "SLC26A2-related_disorder|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|not_provided|3MC_syndrome_2|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|not_provided": 2,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|Achondrogenesis|_type_IB": 3,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 2,
    "Connective_tissue_disorder|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|not_provided|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|not_specified": 1,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Atelosteogenesis_type_II|Diastrophic_dysplasia": 5,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Osteochondrodysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB|not_provided": 1,
    "Achondrogenesis|_type_IB|not_provided|Inborn_genetic_diseases|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 1,
    "not_provided|Achondrogenesis|_type_IB": 1,
    "Osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB": 1,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|not_specified": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Osteochondrodysplasia|Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB|not_provided": 1,
    "Achondrogenesis|_type_IB|not_specified|not_provided|Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 1,
    "not_specified|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|not_specified": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB": 9,
    "Connective_tissue_disorder|SLC26A2-related_disorder|Inborn_genetic_diseases|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|not_provided|3MC_syndrome_2|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 9,
    "Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia": 8,
    "Inborn_genetic_diseases|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 2,
    "Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|not_provided": 1,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Connective_tissue_disorder|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|not_specified|not_provided|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Osteochondrodysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|not_provided|Atelosteogenesis_type_II|Diastrophic_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Inborn_genetic_diseases": 1,
    "not_provided|Connective_tissue_disorder|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Connective_tissue_disorder|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II": 2,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Inborn_genetic_diseases": 2,
    "not_provided|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia": 2,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|not_specified|Sulfate_transporter-related_osteochondrodysplasia|not_provided": 1,
    "Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB": 2,
    "Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia": 2,
    "Inborn_genetic_diseases|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|not_provided|Inborn_genetic_diseases": 1,
    "Diastrophic_dysplasia|Diastrophic_dysplasia|_broad_bone-platyspondylic_variant": 1,
    "Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|not_specified|Sulfate_transporter-related_osteochondrodysplasia|not_provided": 1,
    "Osteochondrodysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia": 1,
    "Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Connective_tissue_disorder|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|not_specified|not_provided|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|Connective_tissue_disorder": 1,
    "Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|not_provided|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|De_la_Chapelle_dysplasia|Osteochondrodysplasia": 1,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB": 1,
    "SLC26A2-related_disorder": 2,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia": 2,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 2,
    "Diastrophic_dysplasia|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|not_provided|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Connective_tissue_disorder|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|not_provided": 1,
    "not_provided|Multiple_epiphyseal_dysplasia_type_4|SLC26A2-related_disorder|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 2,
    "Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|not_provided": 1,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|not_provided|Connective_tissue_disorder|not_specified|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|not_specified": 2,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia": 1,
    "SLC26A2-related_disorder|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II": 1,
    "Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|SLC26A2-related_disorder": 1,
    "Diastrophic_dysplasia|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia": 2,
    "Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|SLC26A2-related_disorder|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|not_provided|3MC_syndrome_2|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Osteochondrodysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Osteochondrodysplasia|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia|not_provided|not_specified|Connective_tissue_disorder": 1,
    "Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|not_provided|not_specified": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Atelosteogenesis_type_II|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|not_provided|not_specified|Sulfate_transporter-related_osteochondrodysplasia|Connective_tissue_disorder": 1,
    "Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 5,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II": 2,
    "Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 4,
    "Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4": 2,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia": 2,
    "Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|not_provided|Diastrophic_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Sulfate_transporter-related_osteochondrodysplasia": 4,
    "Atelosteogenesis_type_II|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|not_provided|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 1,
    "Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|not_provided|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Diastrophic_dysplasia|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 3,
    "Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4": 2,
    "Achondrogenesis|_type_IB|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 2,
    "Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Atelosteogenesis_type_II": 5,
    "Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|Atelosteogenesis": 2,
    "Diastrophic_dysplasia|Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 6,
    "Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|not_provided|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|Atelosteogenesis": 1,
    "Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|not_provided|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 2,
    "Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Achondrogenesis|_type_IB|Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 11,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|not_provided|Diastrophic_dysplasia|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Diastrophic_dysplasia|Sulfate_transporter-related_osteochondrodysplasia": 1,
    "Diastrophic_dysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia|Atelosteogenesis_type_II": 5,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|not_provided|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II": 2,
    "Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|not_provided|Atelosteogenesis_type_II|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4": 1,
    "Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia|Achondrogenesis|Atelosteogenesis": 3,
    "Sulfate_transporter-related_osteochondrodysplasia|Diastrophic_dysplasia|Multiple_epiphyseal_dysplasia_type_4|Achondrogenesis|Atelosteogenesis": 1,
    "not_provided|Multiple_epiphyseal_dysplasia_type_4|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Diastrophic_dysplasia|Atelosteogenesis_type_II": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|Atelosteogenesis": 1,
    "Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia|Achondrogenesis|_type_IB": 1,
    "not_provided|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Atelosteogenesis_type_II|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia": 2,
    "not_provided|Sulfate_transporter-related_osteochondrodysplasia|Multiple_epiphyseal_dysplasia_type_4|Diastrophic_dysplasia|Achondrogenesis|Atelosteogenesis": 1,
    "not_provided|Sulfate_transporter-related_osteochondrodysplasia|Achondrogenesis|_type_IB|Multiple_epiphyseal_dysplasia_type_4|Atelosteogenesis_type_II|Diastrophic_dysplasia": 2,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids": 92,
    "not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 22,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 2,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|not_provided": 1,
    "not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids|CSF1R-related_disorder": 4,
    "not_provided|CSF1R-related_disorder|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "not_provided|CSF1R-related_leukoencephalopathy": 1,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 11,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided": 29,
    "not_specified|not_provided|CSF1R-related_disorder|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 3,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|not_provided": 1,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 11,
    "CSF1R-related_disorder|not_specified": 1,
    "not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids|CSF1R-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided": 3,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 1,
    "not_provided|Frontotemporal_dementia": 34,
    "Alzheimer_disease": 256,
    "CSF1R-related_disorder|not_provided": 13,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 2,
    "CSF1R-related_leukoencephalopathy": 1,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 2,
    "not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 1,
    "CSF1R-Related_Adult-Onset_Leukoencephalopathy|not_provided": 1,
    "not_provided|CSF1R-related_disorder": 10,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|CSF1R-related_disorder|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 2,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "CSF1R-related_disorder|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "Cerebral_arterial_disease": 2,
    "Inborn_genetic_diseases|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 1,
    "not_provided|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 3,
    "not_provided|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "not_specified|Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided": 1,
    "CSF1R-related_disorder|Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|CSF1R-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 1,
    "CSF1R-related_disorder": 11,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|not_provided": 5,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|not_provided": 1,
    "not_provided|CSF1R-related_disorder|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "not_provided|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 2,
    "Inborn_genetic_diseases|CSF1R-related_disorder|not_provided": 1,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|not_provided": 1,
    "not_specified|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 1,
    "Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided|CSF1R-related_disorder|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 1,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided|CSF1R-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|CSF1R-related_disorder": 1,
    "not_provided|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 2,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 2,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1": 2,
    "CSF1R-related_disorder|Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided": 1,
    "not_specified|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids|CSF1R-related_disorder": 1,
    "not_specified|Hereditary_diffuse_leukoencephalopathy_with_spheroids|CSF1R-related_disorder|not_provided": 1,
    "CSF1R-related_disorder|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "not_provided|CSF1R-related_disorder|Inborn_genetic_diseases|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Hereditary_diffuse_leukoencephalopathy_with_spheroids|not_provided": 1,
    "Parkinsonian_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis": 1,
    "CSF1R-related_disorder|Brain_abnormalities|_neurodegeneration|_and_dysosteosclerosis|Leukoencephalopathy|_diffuse_hereditary|_with_spheroids_1|not_provided|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "Hereditary_diffuse_leukoencephalopathy_with_spheroids|CSF1R-related_disorder|not_provided|not_specified": 1,
    "Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_provided": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 37,
    "Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 8,
    "PDGFRB-related_disorder|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Myofibromatosis|_infantile|_1|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 10,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 34,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Inborn_genetic_diseases": 4,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 33,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 5,
    "PDGFRB-related_disorder": 23,
    "Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 6,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Myofibromatosis|_infantile|_1|not_specified|not_provided|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 2,
    "Basal_ganglia_calcification|_idiopathic|_4|Parkinsonian_disorder": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis": 5,
    "not_provided|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases": 3,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 18,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 8,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_provided|Myofibromatosis|_infantile|_1|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|not_specified|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Basal_ganglia_calcification|_idiopathic|_4": 4,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|PDGFRB-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|PDGFRB-related_disorder": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 6,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|not_provided": 3,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 50,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|not_provided|Myofibromatosis|_infantile|_1": 1,
    "not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 4,
    "not_provided|PDGFRB-related_disorder": 1,
    "PDGFRB-related_disorder|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_provided": 1,
    "not_provided|PDGFRB-related_disorder|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|PDGFRB-related_disorder": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|not_provided": 2,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4": 4,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 3,
    "not_provided|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|PDGFRB-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Inborn_genetic_diseases": 2,
    "PDGFRB-related_disorder|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|PDGFRB-related_disorder|Myofibromatosis|_infantile|_1|not_provided|not_specified|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Inborn_genetic_diseases|not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis": 1,
    "Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder": 1,
    "Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 4,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 6,
    "Infantile_myofibromatosis": 9,
    "Myofibromatosis|_infantile|_1|not_provided": 1,
    "Myofibromatosis|_infantile|_1": 4,
    "PDGFRB-related_disorder|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|not_specified|not_provided|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|not_provided": 1,
    "not_provided|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 2,
    "not_specified|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 1,
    "Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 4,
    "not_provided|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 3,
    "PDGFRB-related_disorder|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 1,
    "not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis": 3,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|PDGFRB-related_disorder": 2,
    "Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 4,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 1,
    "Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 8,
    "Myofibromatosis|_infantile|_1|Myeloproliferative_disorder|_chronic|_with_eosinophilia|Basal_ganglia_calcification|_idiopathic|_4|Idiopathic_basal_ganglia_calcification_1|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 5,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Intellectual_disability": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Inborn_genetic_diseases": 1,
    "Myofibromatosis|_infantile|_1|Myeloproliferative_disorder|_chronic|_with_eosinophilia|Idiopathic_basal_ganglia_calcification_1|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|not_provided|Infantile_myofibromatosis": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|not_provided|Cerebral_palsy": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 4,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "PDGFRB-related_disorder|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 3,
    "Infantile_myofibromatosis|Myofibromatosis|_infantile|_1|not_provided": 1,
    "Myeloproliferative_disorder|_chronic|_with_eosinophilia|not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|See_cases": 1,
    "Myofibromatosis|_infantile|_1|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|not_provided": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|not_specified|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 3,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder": 1,
    "not_provided|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 2,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|not_specified": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "not_provided|Myofibromatosis|_infantile|_1|Hydrocephalus|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Inborn_genetic_diseases|Dandy-Walker_syndrome": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder": 1,
    "Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Myofibromatosis|_infantile|_1|not_provided": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Inborn_genetic_diseases": 1,
    "PDGFRB-related_disorder|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|PDGFRB-related_disorder": 2,
    "Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases": 1,
    "PDGFRB-related_disorder|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|not_provided": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|not_provided": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis": 6,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|not_provided": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|not_provided": 2,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases|PDGFRB-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|not_specified|not_provided|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myeloproliferative_disorder|_chronic|_with_eosinophilia|Basal_ganglia_calcification|_idiopathic|_4|Myofibromatosis|_infantile|_1|Infantile_myofibromatosis": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_provided|Myofibromatosis|_infantile|_1|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Myofibromatosis|_infantile|_1|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Myeloproliferative_disorder|_chronic|_with_eosinophilia|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Microcephaly|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "Inborn_genetic_diseases|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|not_provided": 1,
    "PDGFRB-related_disorder|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "PDGFRB-related_disorder|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome": 2,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|PDGFRB-related_disorder|not_specified": 1,
    "Myofibromatosis|_infantile|_1|not_specified|not_provided|PDGFRB-related_disorder|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_provided": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_specified|Myofibromatosis|_infantile|_1|not_provided|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "PDGFRB-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|PDGFRB-related_disorder": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|not_specified|not_provided|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Inborn_genetic_diseases|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "not_specified|Inborn_genetic_diseases|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "not_specified|not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4": 2,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Inborn_genetic_diseases": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|not_provided|PDGFRB-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder|not_provided": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder|Inborn_genetic_diseases": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Myofibromatosis|_infantile|_1": 1,
    "PDGFRB-related_disorder|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Myeloproliferative_disorder|_chronic|_with_eosinophilia|Idiopathic_basal_ganglia_calcification_1|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|not_provided|Infantile_myofibromatosis": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|not_specified": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Myofibromatosis|_infantile|_1|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|not_provided": 1,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis": 2,
    "Inborn_genetic_diseases|not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|PDGFRB-related_disorder": 1,
    "Inborn_genetic_diseases|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|not_provided": 1,
    "Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|not_provided|PDGFRB-related_disorder|Myofibromatosis|_infantile|_1|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "not_provided|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 2,
    "Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Infantile_myofibromatosis|PDGFRB-related_disorder|Myofibromatosis|_infantile|_1|not_provided|Myeloproliferative_disorder|_chronic|_with_eosinophilia": 1,
    "PDGFRB-related_disorder|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Basal_ganglia_calcification|_idiopathic|_4|Infantile_myofibromatosis|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4": 1,
    "Inborn_genetic_diseases|Infantile_myofibromatosis|Basal_ganglia_calcification|_idiopathic|_4|Acroosteolysis-keloid-like_lesions-premature_aging_syndrome|Skeletal_overgrowth-craniofacial_dysmorphism-hyperelastic_skin-white_matter_lesions_syndrome": 1,
    "CDX1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_53|Intellectual_disability|_autosomal_recessive_63": 2,
    "Intellectual_disability|_autosomal_recessive_63|Intellectual_disability|_autosomal_dominant_53": 2,
    "Intellectual_disability|_autosomal_recessive_63": 2,
    "Intellectual_disability|_autosomal_dominant_53": 16,
    "not_provided|Intellectual_disability|_autosomal_dominant_53|Intellectual_disability|_autosomal_recessive_63": 2,
    "CAMK2A-related_disorder|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_53|not_provided": 2,
    "not_provided|CAMK2A-related_disorder": 1,
    "CAMK2A-related_disorder": 4,
    "Intellectual_disability|_autosomal_dominant_53|Intellectual_disability": 4,
    "Intellectual_disability|_autosomal_recessive_63|not_provided|Autism_spectrum_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_53": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_53|not_specified": 1,
    "Intellectual_disability|not_provided|Intellectual_disability|_autosomal_dominant_53": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_53": 1,
    "Intellectual_disability|_autosomal_dominant_53|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_53": 1,
    "Intellectual_disability|_autosomal_dominant_53|Global_developmental_delay": 1,
    "ARSI-related_disorder|not_provided": 1,
    "Spastic_paraplegia|ARSI-related_disorder|not_provided": 1,
    "ARSI-related_disorder|Spastic_paraplegia": 4,
    "ARSI-related_disorder|Spastic_paraplegia|not_specified": 1,
    "Spastic_paraplegia|ARSI-related_disorder": 1,
    "ARSI-related_disorder": 1,
    "Treacher_Collins_syndrome_1": 429,
    "Treacher_Collins_Syndrome|_Dominant|not_provided": 1,
    "not_provided|Treacher_Collins_syndrome_1": 51,
    "Treacher_Collins_syndrome_1|not_provided": 38,
    "TCOF1-related_disorder": 29,
    "not_specified|not_provided|Treacher_Collins_syndrome_1": 9,
    "Treacher_Collins_syndrome_1|Inborn_genetic_diseases": 20,
    "Treacher_Collins_syndrome_1|not_provided|not_specified": 5,
    "Treacher_Collins_syndrome_1|TCOF1-related_disorder": 13,
    "Treacher_Collins_syndrome_1|not_provided|Inborn_genetic_diseases|TCOF1-related_disorder": 1,
    "TCOF1-related_disorder|Treacher_Collins_syndrome_1": 9,
    "Inborn_genetic_diseases|Treacher_Collins_syndrome_1": 15,
    "not_provided|Treacher_Collins_syndrome_1|TCOF1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Treacher_Collins_syndrome_1|TCOF1-related_disorder": 1,
    "Treacher_Collins_syndrome_1|not_specified": 4,
    "Treacher_Collins_syndrome_1|not_specified|not_provided": 1,
    "not_provided|TCOF1-related_disorder|Treacher_Collins_syndrome_1": 1,
    "not_provided|Treacher_Collins_syndrome_1|TCOF1-related_disorder": 4,
    "Treacher_Collins_syndrome_1|Treacher_Collins_syndrome": 1,
    "not_provided|Treacher_Collins_syndrome_1|Inborn_genetic_diseases": 7,
    "not_provided|TCOF1-related_disorder": 4,
    "Inborn_genetic_diseases|TCOF1-related_disorder|not_specified": 2,
    "Treacher_Collins_syndrome_1|Inborn_genetic_diseases|not_provided": 6,
    "TCOF1-related_disorder|not_specified|Treacher_Collins_syndrome_1|not_provided": 1,
    "Treacher_Collins_syndrome_1|TCOF1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TCOF1-related_disorder|not_provided": 4,
    "Treacher_Collins_syndrome|not_provided|Treacher_Collins_syndrome_1": 1,
    "TCOF1-related_disorder|Treacher_Collins_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Treacher_Collins_syndrome": 4,
    "Treacher_Collins_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|TCOF1-related_disorder|Inborn_genetic_diseases|Treacher_Collins_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|TCOF1-related_disorder|Treacher_Collins_syndrome_1": 1,
    "TCOF1-related_disorder|not_specified|not_provided|Treacher_Collins_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Treacher_Collins_syndrome_1": 1,
    "Treacher_Collins_syndrome_1|TCOF1-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Treacher_Collins_syndrome_1|TCOF1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Treacher_Collins_syndrome_1": 6,
    "Treacher_Collins_syndrome_1|not_provided|TCOF1-related_disorder": 3,
    "not_specified|TCOF1-related_disorder": 1,
    "not_provided|not_specified|Treacher_Collins_syndrome_1": 3,
    "TCOF1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Treacher_Collins_syndrome_1|not_specified": 4,
    "not_specified|TCOF1-related_disorder|Treacher_Collins_syndrome_1": 1,
    "not_specified|Treacher_Collins_syndrome_1": 1,
    "TCOF1-related_disorder|Treacher_Collins_syndrome_1|not_provided": 1,
    "not_specified|not_provided|Treacher_Collins_syndrome_1|TCOF1-related_disorder|Treacher_Collins_syndrome": 1,
    "Treacher_Collins_syndrome_1|TCOF1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "TCOF1-related_disorder|Treacher_Collins_syndrome_1|Inborn_genetic_diseases": 1,
    "not_specified|Treacher_Collins_syndrome_1|not_provided": 3,
    "Treacher_Collins_Syndrome|_Dominant|Treacher_Collins_syndrome_1": 1,
    "Inborn_genetic_diseases|TCOF1-related_disorder|Treacher_Collins_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Treacher_Collins_syndrome_1|not_provided": 3,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 29,
    "not_provided|not_specified|Inborn_genetic_diseases|Treacher_Collins_syndrome_1": 1,
    "Inborn_genetic_diseases|Cleft_lip/palate|not_provided|Treacher_Collins_syndrome_1": 1,
    "TCOF1-related_disorder|not_provided|Treacher_Collins_syndrome_1": 1,
    "not_provided|TCOF1-related_disorder|not_specified|Treacher_Collins_syndrome_1": 1,
    "Treacher_Collins_Syndrome|_Dominant": 2,
    "TCOF1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TCOF1-related_disorder|Inborn_genetic_diseases|Treacher_Collins_syndrome_1|Treacher_Collins_syndrome": 1,
    "not_provided|Hearing_impairment|Treacher_Collins_syndrome_1": 1,
    "not_provided|not_specified|Treacher_Collins_syndrome_1|TCOF1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Treacher_Collins_syndrome_1|Treacher_Collins_syndrome": 1,
    "Microcephaly|not_provided|Treacher_Collins_syndrome_1|Inborn_genetic_diseases": 1,
    "RPS14-related_condition": 2,
    "NDST1-related_disorder": 5,
    "Intellectual_disability|_autosomal_recessive_46|not_provided": 4,
    "NDST1-related_disorder|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_46": 13,
    "Intellectual_disability|_autosomal_recessive_46|Intellectual_disability|not_provided|Inborn_genetic_diseases|NDST1-related_disorder|not_specified": 1,
    "NDST1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_46|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_46|Inborn_genetic_diseases": 2,
    "Cleft_lip/palate": 8,
    "not_provided|NDST1-related_disorder": 4,
    "not_provided|Intellectual_disability|_autosomal_recessive_46": 2,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_recessive_46": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_46|Inborn_genetic_diseases": 1,
    "NDST1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_46|not_provided|not_specified": 1,
    "Intellectual_disability|not_provided|not_specified|NDST1-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_46|not_provided|Global_developmental_delay|See_cases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_46": 1,
    "SYNPO-related_disorder": 1,
    "Nephrotic_syndrome|Focal_segmental_glomerulosclerosis_8": 1,
    "not_provided|SYNPO-related_disorder": 1,
    "RBM22-related_disorder|not_provided": 1,
    "RBM22-related_disorder": 1,
    "IRGM-related_disorder|not_provided": 1,
    "not_specified|Inflammatory_bowel_disease_19": 1,
    "IRGM-related_disorder": 1,
    "Tay-Sachs_disease|_variant_AB": 167,
    "not_provided|Tay-Sachs_disease|_variant_AB": 5,
    "Inborn_genetic_diseases|Tay-Sachs_disease|_variant_AB": 6,
    "Tay-Sachs_disease|_variant_AB|GM2A-related_condition": 1,
    "Tay-Sachs_disease|_variant_AB|not_specified|not_provided": 2,
    "Tay-Sachs_disease|_variant_AB|not_provided": 8,
    "Neurodegenerative_illness_progressing_to_crippling_dystonia_and_death_with_relentless_cerebral_atrophy|Tay-Sachs_disease|_variant_AB": 1,
    "not_specified|not_provided|Tay-Sachs_disease|_variant_AB": 3,
    "Tay-Sachs_disease|Tay-Sachs_disease|_variant_AB": 3,
    "Tay-Sachs_disease|_variant_AB|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Tay-Sachs_disease|_variant_AB|not_provided": 1,
    "SLC36A2-related_disorder|not_provided": 5,
    "Hyperglycinuria|Iminoglycinuria|not_provided": 8,
    "SLC36A2-related_disorder": 2,
    "not_provided|SLC36A2-related_disorder": 3,
    "not_specified|Iminoglycinuria|Hyperglycinuria": 1,
    "Hyperglycinuria|Iminoglycinuria|SLC36A2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Iminoglycinuria|Hyperglycinuria": 1,
    "SLC36A2-related_disorder|not_provided|Iminoglycinuria|Hyperglycinuria": 1,
    "FAT2-related_disorder|not_provided": 27,
    "Spinocerebellar_ataxia_45": 19,
    "FAT2-related_disorder|not_specified|not_provided": 3,
    "FAT2-related_disorder|not_provided|Spinocerebellar_ataxia_45": 6,
    "FAT2-related_disorder": 9,
    "not_specified|not_provided|FAT2-related_disorder|Spinocerebellar_ataxia_45": 1,
    "not_provided|FAT2-related_disorder|not_specified": 4,
    "not_provided|Spinocerebellar_ataxia_45|FAT2-related_disorder": 12,
    "not_provided|FAT2-related_disorder": 16,
    "not_provided|not_specified|Spinocerebellar_ataxia_45": 1,
    "Spinocerebellar_ataxia_45|FAT2-related_disorder|not_provided": 4,
    "FAT2-related_disorder|not_provided|not_specified": 3,
    "Spinocerebellar_ataxia_45|not_specified": 3,
    "not_specified|Spinocerebellar_ataxia_45": 2,
    "not_specified|not_provided|Spinocerebellar_ataxia_45": 1,
    "FAT2-related_disorder|not_specified": 2,
    "FAT2-related_disorder|Spinocerebellar_ataxia_45|not_provided": 3,
    "not_specified|not_provided|FAT2-related_disorder": 2,
    "Cerebellar_ataxia|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_45|not_specified|not_provided": 1,
    "not_provided|not_specified|FAT2-related_disorder": 2,
    "not_provided|Spinocerebellar_ataxia_45": 1,
    "Spinocerebellar_ataxia_45|FAT2-related_disorder|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_45|not_provided": 3,
    "not_provided|Spastic_ataxia|not_specified": 1,
    "Spinocerebellar_ataxia_45|not_provided|FAT2-related_disorder": 1,
    "not_provided|Osteogenesis_imperfecta_type_17": 3,
    "Osteogenesis_imperfecta_type_17": 4,
    "SPARC-related_disorder": 5,
    "not_provided|Osteogenesis_imperfecta|SPARC-related_disorder": 1,
    "SPARC-related_disorder|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Osteogenesis_imperfecta": 2,
    "Inborn_genetic_diseases|SPARC-related_disorder|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|SPARC-related_disorder": 2,
    "not_provided|SPARC-related_disorder|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta_type_17|not_provided": 2,
    "SPARC-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_17|not_provided": 1,
    "Osteogenesis_imperfecta_type_17|Osteogenesis_imperfecta|not_provided": 2,
    "Hyperekplexia_1|Hereditary_hyperekplexia": 12,
    "Hereditary_hyperekplexia": 323,
    "Seizure|Inborn_genetic_diseases|Hereditary_hyperekplexia": 1,
    "Hereditary_hyperekplexia|Inborn_genetic_diseases": 11,
    "Hyperekplexia_1": 35,
    "not_provided|Hereditary_hyperekplexia|Inborn_genetic_diseases": 2,
    "Hereditary_hyperekplexia|not_provided|Hyperekplexia_1": 3,
    "Hyperekplexia_1|Hereditary_hyperekplexia|Inborn_genetic_diseases": 6,
    "not_specified|Hereditary_hyperekplexia|Inborn_genetic_diseases|Hyperekplexia_1": 1,
    "Hereditary_hyperekplexia|not_provided": 9,
    "Inborn_genetic_diseases|Hereditary_hyperekplexia": 4,
    "not_provided|Hyperekplexia_1|Hereditary_hyperekplexia": 8,
    "not_specified|Hyperekplexia_1": 1,
    "not_provided|Hereditary_hyperekplexia|Inborn_genetic_diseases|Hyperekplexia_1": 1,
    "not_provided|Hyperekplexia_1|GLRA1-related_disorder|Hereditary_hyperekplexia": 2,
    "Hereditary_hyperekplexia|GLRA1-related_disorder": 3,
    "not_provided|Hereditary_hyperekplexia": 10,
    "Hereditary_hyperekplexia|not_specified": 5,
    "GLRA1-related_disorder|Hereditary_hyperekplexia|not_provided|Hyperekplexia_1": 1,
    "not_specified|Hereditary_hyperekplexia": 4,
    "Hyperekplexia_1|Hereditary_hyperekplexia|GLRA1-related_disorder|not_specified|not_provided": 1,
    "GLRA1-related_disorder|Hereditary_hyperekplexia": 2,
    "not_provided|Hyperekplexia_1|Hereditary_hyperekplexia|Inborn_genetic_diseases": 1,
    "Hereditary_hyperekplexia|Hyperekplexia_1": 8,
    "not_provided|Hereditary_hyperekplexia|Hyperekplexia_1": 1,
    "Hereditary_hyperekplexia|Hyperekplexia_1|not_provided": 1,
    "Hyperekplexia_1|not_provided": 3,
    "Hyperekplexia_1|not_provided|Hereditary_hyperekplexia": 3,
    "Hereditary_hyperekplexia|Inborn_genetic_diseases|not_provided|Hyperekplexia_1": 1,
    "Hyperekplexia_1|GLRA1-related_disorder": 1,
    "GLRA1-related_disorder": 1,
    "not_provided|Hyperekplexia_1": 2,
    "Hyperekplexia_1|GLRA1-related_disorder|Hereditary_hyperekplexia": 2,
    "Hyperekplexia_1|Hereditary_hyperekplexia|GLRA1-related_disorder": 1,
    "GLRA1-related_disorder|Hereditary_hyperekplexia|not_provided": 1,
    "not_specified|not_provided|Hereditary_hyperekplexia": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_hyperekplexia": 1,
    "GRIA1-related_disorder|not_specified": 1,
    "GRIA1-related_disorder|not_provided": 4,
    "Intellectual_developmental_disorder|_autosomal_dominant_67": 15,
    "GRIA1-related_disorder": 15,
    "not_provided|GRIA1-related_disorder": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_76": 2,
    "Inborn_genetic_diseases|not_provided|GRIA1-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_67|not_provided|Intellectual_disability": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_67|Non-syndromic_intellectual_disability|Autism_spectrum_disorder": 1,
    "GALNT10-related_disorder": 2,
    "Hypoplastic_left_heart_syndrome": 124,
    "Hypoplastic_left_heart_syndrome|HAND1-related_disorder": 3,
    "not_specified|Hypoplastic_left_heart_syndrome": 9,
    "Hypoplastic_left_heart_syndrome|HAND1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Hypoplastic_left_heart_syndrome|not_provided": 1,
    "Hypoplastic_left_heart_syndrome|not_specified": 2,
    "not_provided|HAND1-related_disorder|Hypoplastic_left_heart_syndrome|not_specified": 1,
    "HAND1-related_disorder|Hypoplastic_left_heart_syndrome": 1,
    "not_provided|Hypoplastic_left_heart_syndrome": 1,
    "HAND1-related_disorder|Hypoplastic_left_heart_syndrome|not_provided": 1,
    "not_provided|Hypoplastic_left_heart_syndrome|not_specified": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_motor_dysfunction": 30,
    "GEMIN5-related_disorder": 5,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_motor_dysfunction|not_provided": 3,
    "Inborn_genetic_diseases|GEMIN5-related_disorder": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_motor_dysfunction": 1,
    "not_provided|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_motor_dysfunction": 1,
    "GEMIN5-related_disorder|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_motor_dysfunction|GEMIN5-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "GEMIN5-related_disorder|not_provided": 1,
    "not_specified|GEMIN5-related_disorder": 1,
    "KIF4B-related_disorder": 16,
    "KIF4B-related_disorder|not_provided": 2,
    "not_provided|KIF4B-related_disorder": 3,
    "Small_for_gestational_age|Large_for_gestational_age": 1,
    "not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 2,
    "not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 2,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_specified|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|not_specified": 1,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 48,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 21,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Limb-girdle_muscular_dystrophy|_recessive|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified": 2,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 7,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy": 3,
    "not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_provided": 4,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 275,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided": 5,
    "SGCD-related_disorder": 7,
    "not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified|not_provided": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 8,
    "Dilated_cardiomyopathy_1L": 8,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Cardiomyopathy|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases": 8,
    "Primary_familial_dilated_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Cardiomyopathy|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|Cardiomyopathy|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Inborn_genetic_diseases": 5,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|not_provided|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "not_specified|SGCD-related_disorder|Cardiomyopathy|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 5,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 30,
    "not_specified|not_provided|Cardiomyopathy|Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Cardiovascular_phenotype|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_specified|not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Neuromuscular_disease|Dilated_cardiomyopathy_1L": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Inborn_genetic_diseases": 2,
    "not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|not_provided": 2,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|not_provided": 1,
    "Dilated_cardiomyopathy_1L|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_specified": 1,
    "Neuromuscular_disease|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "Inborn_genetic_diseases|SGCD-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Cardiomyopathy|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "MUSCULAR_DYSTROPHY|_LIMB-GIRDLE|_AUTOSOMAL_RECESSIVE_6|_DIGENIC|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|Dilated_cardiomyopathy_1L|not_provided": 1,
    "Dilated_cardiomyopathy_1L|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L": 1,
    "not_specified|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_specified|Cardiomyopathy|SGCD-related_disorder|Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|SGCD-related_disorder|Inborn_genetic_diseases|not_specified|Cardiomyopathy|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Inborn_genetic_diseases|Dilated_cardiomyopathy_1L": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Inborn_genetic_diseases|SGCD-related_disorder|not_provided|not_specified": 1,
    "SGCD-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|SGCD-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "not_provided|SGCD-related_disorder|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_provided|not_specified": 1,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "SGCD-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_specified|Dilated_cardiomyopathy_1A": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Limb-girdle_muscular_dystrophy|_recessive": 5,
    "not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_specified|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Dilated_cardiomyopathy_1L|Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Cardiomyopathy": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Inborn_genetic_diseases|not_provided": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Inborn_genetic_diseases": 1,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|SGCD-related_disorder|not_specified|not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Hypertrophic_cardiomyopathy_1|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Dilated_cardiomyopathy_1L|not_specified|Cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 1,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 10,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Limb-girdle_muscular_dystrophy|_recessive": 30,
    "not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Limb-girdle_muscular_dystrophy|_recessive": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 12,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Limb-girdle_muscular_dystrophy|_recessive": 5,
    "Limb-girdle_muscular_dystrophy|_recessive|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F": 6,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive": 4,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Limb-girdle_muscular_dystrophy|_recessive": 2,
    "not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Limb-girdle_muscular_dystrophy|_recessive": 2,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_provided|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Limb-girdle_muscular_dystrophy|_recessive": 2,
    "not_provided|Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 3,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 5,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 3,
    "Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 4,
    "Dilated_cardiomyopathy_1L|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_Cardiomyopathy|_Dominant|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|Dilated_cardiomyopathy_1L|Limb-girdle_muscular_dystrophy|_recessive": 6,
    "Qualitative_or_quantitative_defects_of_delta-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Dilated_cardiomyopathy_1L|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2F|not_provided|Dilated_cardiomyopathy_1L|Limb-girdle_muscular_dystrophy|_recessive|Qualitative_or_quantitative_defects_of_delta-sarcoglycan": 1,
    "HAVCR1-related_disorder": 12,
    "not_provided|HAVCR1-related_disorder": 2,
    "not_provided|HAVCR2-related_disorder": 2,
    "HAVCR2-related_disorder": 4,
    "Subcutaneous_panniculitis-like_T-cell_lymphoma": 3,
    "Subcutaneous_panniculitis-like_T-cell_lymphoma|not_specified": 1,
    "HAVCR2-related_disorder|not_specified": 1,
    "Subcutaneous_panniculitis-like_T-cell_lymphoma|HAVCR2-related_disorder|not_provided": 2,
    "Subcutaneous_panniculitis-like_T-cell_lymphoma|not_provided": 1,
    "Lymphoproliferative_syndrome_1": 425,
    "Autoinflammatory_syndrome|Lymphoproliferative_syndrome_1": 2,
    "Lymphoproliferative_syndrome_1|Autoinflammatory_syndrome": 6,
    "Lymphoproliferative_syndrome_1|Inborn_genetic_diseases": 13,
    "not_provided|ITK-related_disorder|Lymphoproliferative_syndrome_1": 1,
    "not_specified|Lymphoproliferative_syndrome_1|ITK-related_disorder": 1,
    "not_provided|Lymphoproliferative_syndrome_1": 12,
    "not_specified|Lymphoproliferative_syndrome_1": 2,
    "Inborn_genetic_diseases|Lymphoproliferative_syndrome_1": 8,
    "Lymphoproliferative_syndrome_1|Autoinflammatory_syndrome|not_specified": 1,
    "Lymphoproliferative_disorder|Lymphoproliferative_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Lymphoproliferative_syndrome_1": 1,
    "ITK-related_disorder|Lymphoproliferative_syndrome_1": 2,
    "ITK-related_disorder": 4,
    "not_specified|Lymphoproliferative_syndrome_1|Autoinflammatory_syndrome": 2,
    "ITK-related_disorder|Autoinflammatory_syndrome|Lymphoproliferative_syndrome_1": 1,
    "Lymphoproliferative_syndrome_1|not_provided": 5,
    "Lymphoproliferative_syndrome_1|ITK-related_disorder": 2,
    "Lymphoproliferative_syndrome_1|not_specified": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Lymphoproliferative_syndrome_1": 1,
    "not_provided|Lymphoproliferative_syndrome_1|Autoinflammatory_syndrome|ITK-related_disorder": 1,
    "ITK-related_disorder|Lymphoproliferative_syndrome_1|not_provided": 1,
    "Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Lymphoproliferative_syndrome_1": 1,
    "Autoinflammatory_syndrome|Lymphoproliferative_syndrome_1|ITK-related_disorder|not_provided": 1,
    "not_specified|Autoinflammatory_syndrome|Lymphoproliferative_syndrome_1|not_provided": 1,
    "Lymphoproliferative_disorder": 17,
    "not_provided|Developmental_and_epileptic_encephalopathy|_65": 12,
    "CYFIP2-related_disorder|Developmental_and_epileptic_encephalopathy|_65": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_65|not_provided|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_65": 30,
    "Global_developmental_delay|Developmental_and_epileptic_encephalopathy|_65": 1,
    "CYFIP2-related_disorder|not_provided": 6,
    "not_provided|CYFIP2-related_disorder": 7,
    "CYFIP2-related_disorder": 6,
    "Developmental_and_epileptic_encephalopathy|_65|not_provided": 8,
    "CYFIP2-related_neurodevelopmental_disorders|not_provided": 1,
    "Intellectual_disability|not_provided|Developmental_and_epileptic_encephalopathy|_65": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_65": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_65|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_65": 1,
    "Developmental_and_epileptic_encephalopathy|_65|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_congenital_ichthyosis_6": 71,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_6": 2,
    "Autosomal_recessive_congenital_ichthyosis_6|not_provided": 8,
    "not_provided|NIPAL4-related_disorder|Autosomal_recessive_congenital_ichthyosis_6": 1,
    "Autosomal_recessive_congenital_ichthyosis_6|not_specified": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_6|Lamellar_ichthyosis": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_6": 3,
    "NIPAL4-related_disorder|not_provided|Autosomal_recessive_congenital_ichthyosis_6": 1,
    "Autosomal_recessive_congenital_ichthyosis_6|Lamellar_ichthyosis|not_provided": 2,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_6": 6,
    "Autosomal_recessive_congenital_ichthyosis|Autosomal_recessive_congenital_ichthyosis_6|Lamellar_ichthyosis|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_6": 2,
    "Autosomal_recessive_congenital_ichthyosis|Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_6": 1,
    "Autosomal_recessive_congenital_ichthyosis": 5,
    "Autosomal_recessive_congenital_ichthyosis_6|NIPAL4-related_disorder": 1,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_6": 1,
    "not_provided|NIPAL4-related_disorder": 1,
    "THG1L-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia|_autosomal_recessive_28": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_28|THG1L-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive_28": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_28": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_28": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_28|not_provided": 1,
    "not_specified|LSM11-related_disorder": 1,
    "Aicardi-Goutieres_syndrome_8": 1,
    "LSM11-related_disorder": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency": 184,
    "Familial_Atypical_Mycobacteriosis|_Autosomal_Recessive": 6,
    "Inborn_genetic_diseases|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency": 11,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency|Inborn_genetic_diseases": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency|IL12B-related_disorder": 3,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency": 2,
    "IL12B-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency": 3,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency|not_provided": 3,
    "Autosomal_recessive_mendelian_susceptibility_to_mycobacterial_diseases_due_to_a_complete_deficiency|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12B_deficiency": 1,
    "ATP10B-associated_developmental_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_92|Intellectual_disability": 6,
    "GABRB2-related_epileptic_encephalopathy|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy_92": 33,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy_92": 5,
    "GABRB2-related_disorder|not_specified|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|GABRB2-related_disorder": 1,
    "See_cases|Intellectual_disability": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_92": 3,
    "GABRB2-related_disorder|not_provided|Intellectual_disability": 2,
    "Developmental_and_epileptic_encephalopathy_92|Intellectual_disability|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_92|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_92|Seizure|Intellectual_disability|not_provided": 1,
    "not_provided|GABRB2-related_disorder|Intellectual_disability": 1,
    "Cerebral_visual_impairment_and_intellectual_disability|Developmental_and_epileptic_encephalopathy_92": 1,
    "GABRB2-related_disorder|Intellectual_disability|not_specified": 1,
    "Intellectual_disability|not_specified|not_provided": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy_92|not_provided": 1,
    "Prostate_cancer|Intellectual_disability|See_cases": 1,
    "Intellectual_disability|not_provided|not_specified|GABRB2-related_disorder": 1,
    "Intellectual_disability|not_provided|Developmental_and_epileptic_encephalopathy_92": 1,
    "GABRB2-related_neurodevelopmental_disorders": 1,
    "GABRB2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_92|not_specified|not_provided": 1,
    "Childhood_absence_epilepsy|GABRA6-related_disorder": 4,
    "Childhood_absence_epilepsy": 15,
    "GABRA6-related_disorder": 3,
    "not_provided|GABRA6-related_disorder|Childhood_absence_epilepsy": 1,
    "GABRA6-related_disorder|Childhood_absence_epilepsy": 1,
    "not_provided|GABRA6-related_disorder": 1,
    "GABRA6-related_disorder|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 73,
    "Juvenile_myoclonic_epilepsy|not_provided": 13,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 5,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_provided": 8,
    "Developmental_and_epileptic_encephalopathy|_19": 26,
    "not_specified|Developmental_and_epileptic_encephalopathy|_19": 1,
    "not_provided|Juvenile_myoclonic_epilepsy": 13,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_specified": 1,
    "GABRA1-related_disorder|not_specified|not_provided|Juvenile_myoclonic_epilepsy": 1,
    "Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy": 26,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 61,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|not_specified": 5,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 104,
    "Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 19,
    "not_specified|not_provided|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|GABRA1-related_disorder": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Developmental_and_epileptic_encephalopathy|_19|Juvenile_myoclonic_epilepsy": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy": 49,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|not_provided": 5,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 9,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|not_provided|Inborn_genetic_diseases": 3,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 39,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_specified|not_provided": 1,
    "not_specified|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 4,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Developmental_and_epileptic_encephalopathy|_19": 3,
    "Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Developmental_and_epileptic_encephalopathy|_19|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Developmental_and_epileptic_encephalopathy|_19|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_19|not_specified|not_provided": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy": 4,
    "not_provided|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 6,
    "not_provided|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 5,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Developmental_and_epileptic_encephalopathy|_19": 2,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_specified": 2,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_provided": 3,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Inborn_genetic_diseases|not_provided": 2,
    "Sensorineural_hearing_loss_disorder|Intellectual_disability|Seizure|not_provided|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_specified|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 1,
    "Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_specified": 2,
    "Juvenile_myoclonic_epilepsy": 36,
    "Inborn_genetic_diseases|not_provided|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Developmental_and_epileptic_encephalopathy|_19|not_provided|Epilepsy": 1,
    "not_provided|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy": 2,
    "Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|not_provided": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|not_provided": 4,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|not_provided": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Developmental_and_epileptic_encephalopathy|_19": 1,
    "GABRA1-related_disorder|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|not_specified|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|not_specified": 3,
    "Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_provided": 3,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 2,
    "Developmental_and_epileptic_encephalopathy|_19|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 1,
    "GABRA1-related_disorder|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_specified|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy": 1,
    "GABRA1-related_disorder": 3,
    "not_provided|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Developmental_and_epileptic_encephalopathy|_19": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|not_specified|not_provided": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Developmental_and_epileptic_encephalopathy|_19|not_provided|Intractable_seizure": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Developmental_and_epileptic_encephalopathy|_19|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_19|not_provided": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Developmental_and_epileptic_encephalopathy|_19": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Developmental_and_epileptic_encephalopathy|_19": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_19": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|not_specified": 1,
    "not_specified|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|not_provided": 1,
    "not_provided|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|not_specified": 1,
    "not_provided|not_specified|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|GABRA1-related_disorder": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_19": 2,
    "not_provided|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 1,
    "Developmental_and_epileptic_encephalopathy|_19|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy": 2,
    "Developmental_and_epileptic_encephalopathy|_19|Intellectual_disability": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Developmental_and_epileptic_encephalopathy|_19|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 1,
    "Epilepsy|_childhood_absence_4": 1,
    "not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Developmental_and_epileptic_encephalopathy|_19|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 1,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4": 1,
    "Inborn_genetic_diseases|not_specified|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4": 1,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Developmental_and_epileptic_encephalopathy|_19": 1,
    "Developmental_and_epileptic_encephalopathy|_19|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|not_provided|Inborn_genetic_diseases": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_19": 1,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence_4|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13": 1,
    "Marfanoid_habitus_and_intellectual_disability|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Developmental_and_epileptic_encephalopathy|_19|not_provided": 1,
    "Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Inborn_genetic_diseases": 1,
    "not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy": 1,
    "GABRA1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_idiopathic_generalized|_susceptibility_to|_13|Epilepsy|_childhood_absence_4|not_specified|not_provided": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 47,
    "not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 6,
    "Severe_myoclonic_epilepsy_in_infancy|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus": 1,
    "Severe_myoclonic_epilepsy_in_infancy|Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 255,
    "Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 74,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_specified": 9,
    "Inborn_genetic_diseases|not_provided|GABRG2-related_disorder|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 2,
    "Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 6,
    "not_provided|Inborn_genetic_diseases|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 1,
    "not_specified|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 10,
    "not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Inborn_genetic_diseases": 2,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Inborn_genetic_diseases": 6,
    "not_provided|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 8,
    "Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_specified|not_provided": 1,
    "not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 23,
    "Developmental_and_epileptic_encephalopathy|_74": 8,
    "Febrile_seizures|_familial|_8": 12,
    "Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided": 9,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided": 22,
    "Febrile_seizures|_familial|_8|Inborn_genetic_diseases": 1,
    "GABRG2-related_disorder|Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus_3|Febrile_seizures|_familial|_8|Developmental_and_epileptic_encephalopathy|_74|Inborn_genetic_diseases": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Developmental_and_epileptic_encephalopathy|_74|Generalized_epilepsy_with_febrile_seizures_plus_3|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_74|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided|Seizure": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Developmental_and_epileptic_encephalopathy|_74|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided": 2,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_specified|Inborn_genetic_diseases|not_provided|Febrile_seizures|_familial|_8": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 1,
    "not_specified|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 2,
    "Developmental_and_epileptic_encephalopathy|_74|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 3,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|GABRG2-related_disorder": 1,
    "Lennox-Gastaut_syndrome|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Developmental_and_epileptic_encephalopathy|_74|Seizure": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided|Developmental_and_epileptic_encephalopathy|_74": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided": 1,
    "GABRG2-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_74|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 1,
    "not_provided|Intellectual_disability|not_specified|GABRG2-related_disorder": 1,
    "not_specified|GABRG2-related_disorder": 1,
    "GABRG2-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_74|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 2,
    "not_provided|Febrile_seizures|_familial|_8|Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 1,
    "Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided|not_specified": 1,
    "GABRG2-related_disorder|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_specified|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_74": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "Developmental_and_epileptic_encephalopathy|_74|Inborn_genetic_diseases": 1,
    "Seizure|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_74": 1,
    "not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|GABRG2-related_disorder": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided|Febrile_seizures|_familial|_8": 1,
    "not_specified|not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 2,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "not_provided|Intellectual_disability|Febrile_seizures|_familial|_8|Developmental_and_epileptic_encephalopathy|_74|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2": 1,
    "Developmental_and_epileptic_encephalopathy|_74|Inborn_genetic_diseases|Self-limited_epilepsy_with_centrotemporal_spikes|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided|Generalized_epilepsy_with_febrile_seizures_plus_3": 1,
    "not_provided|GABRG2-related_disorder|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Seizure": 1,
    "not_provided|GABRG2-related_disorder": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Developmental_and_epileptic_encephalopathy|_74": 1,
    "Inborn_genetic_diseases|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided": 4,
    "GABRG2-related_disorder": 2,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 3,
    "Inborn_genetic_diseases|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Epilepsy|Inborn_genetic_diseases": 1,
    "GABRG2-related_disorder|Inborn_genetic_diseases|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_specified|not_provided": 1,
    "not_specified|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided": 1,
    "not_specified|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8": 1,
    "EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|GABRG2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "GABRG2-related_disorder|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Febrile_seizures|_familial|_8|not_provided": 1,
    "Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|not_provided|Developmental_and_epileptic_encephalopathy|_74": 1,
    "not_provided|Febrile_seizures|_familial|_8|EPILEPSY|_CHILDHOOD_ABSENCE|_SUSCEPTIBILITY_TO|_2|Developmental_and_epileptic_encephalopathy|_74": 1,
    "Breast_cancer|_susceptibility_to": 8,
    "Memory_quantitative_trait_locus": 1,
    "Hypomyelinating_leukodystrophy_9|not_provided": 6,
    "not_provided|Hypomyelinating_leukodystrophy_9|Inborn_genetic_diseases": 2,
    "not_provided|Hypomyelinating_leukodystrophy_9": 6,
    "Hypomyelinating_leukodystrophy_9|not_provided|not_specified": 1,
    "Hypomyelinating_leukodystrophy_9": 14,
    "not_provided|RARS1-related_disorder": 1,
    "not_provided|Hypomyelinating_leukodystrophy_9|Inborn_genetic_diseases|RARS1-related_disorder": 1,
    "Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_9": 1,
    "RARS1-related_disorder|not_provided": 2,
    "RARS1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hypomyelinating_leukodystrophy_9|not_specified|RARS1-related_disorder": 1,
    "RARS1-related_disorder": 2,
    "not_provided|not_specified|RARS1-related_disorder": 1,
    "Hypomyelinating_leukodystrophy_9|Leukodystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_9|not_specified": 1,
    "Hypomyelinating_leukodystrophy_9|not_specified|not_provided": 1,
    "RARS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypomyelinating_leukodystrophy_9|not_specified": 1,
    "Hypomyelinating_leukodystrophy_9|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_9": 1,
    "SLIT3-related_disorder": 11,
    "not_provided|SLIT3-related_disorder": 5,
    "not_specified|SLIT3-related_disorder": 1,
    "SLIT3-related_disorder|not_provided": 2,
    "SLIT3-related_anomalies_of_the_kidney_and_urinary_tract": 3,
    "SLIT3-related_anomalies_of_the_kidney_and_urinary_tract|not_specified": 1,
    "not_specified|SLIT3-related_anomalies_of_the_kidney_and_urinary_tract": 1,
    "Familial_congenital_diaphragmatic_hernia": 1,
    "Severe_primary_microcephaly|Neonatal_death": 1,
    "DOCK2_deficiency": 905,
    "Inborn_genetic_diseases|DOCK2_deficiency": 55,
    "DOCK2_deficiency|Inborn_genetic_diseases": 24,
    "Inborn_genetic_diseases|DOCK2_deficiency|DOCK2-related_disorder|not_provided": 1,
    "DOCK2_deficiency|not_specified": 3,
    "DOCK2-related_disorder": 2,
    "not_provided|DOCK2_deficiency": 15,
    "not_provided|Inborn_genetic_diseases|DOCK2_deficiency": 1,
    "DOCK2-related_disorder|DOCK2_deficiency": 8,
    "DOCK2_deficiency|not_provided": 14,
    "DOCK2_deficiency|DOCK2-related_disorder": 4,
    "DOCK2_deficiency|not_specified|not_provided|DOCK2-related_disorder": 1,
    "not_provided|DOCK2_deficiency|not_specified": 5,
    "not_provided|DOCK2_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|DOCK2_deficiency": 1,
    "DOCK2_deficiency|DOCK2-related_disorder|Inborn_genetic_diseases": 2,
    "See_cases|DOCK2_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|DOCK2_deficiency|DOCK2-related_disorder": 1,
    "See_cases|not_provided|Inborn_genetic_diseases|DOCK2_deficiency": 1,
    "DOCK2_deficiency|DOCK2-related_disorder|not_provided": 1,
    "DOCK2-related_disorder|Inborn_genetic_diseases|not_provided|DOCK2_deficiency": 1,
    "DOCK2_deficiency|See_cases": 1,
    "DOCK2_deficiency|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|DOCK2_deficiency": 1,
    "DOCK2-related_disorder|Inborn_genetic_diseases|DOCK2_deficiency|not_provided": 1,
    "DOCK2_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|DOCK2-related_disorder|DOCK2_deficiency": 1,
    "DOCK2_deficiency|not_provided|DOCK2-related_disorder": 1,
    "Associated_with_severe_COVID-19_disease": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 71,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4": 236,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|FOXI1-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 33,
    "not_provided|FOXI1-related_disorder": 2,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 29,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 25,
    "FOXI1-related_disorder|not_provided": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|not_specified": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "FOXI1-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 2,
    "not_provided|FOXI1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 4,
    "not_specified|not_provided|FOXI1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "FOXI1-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided": 15,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|FOXI1-related_disorder": 1,
    "FOXI1-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 2,
    "Nonsyndromic_Hearing_Loss|_Mixed|Pendred_syndrome": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|FOXI1-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|FOXI1-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|not_provided": 1,
    "FOXI1-related_disorder": 1,
    "Immunodeficiency_81": 4,
    "KCNMB1-related_disorder": 2,
    "HYPERTENSION|_DIASTOLIC|_RESISTANCE_TO": 1,
    "KCNMB1-related_disorder|HYPERTENSION|_DIASTOLIC|_RESISTANCE_TO": 1,
    "RANBP17-related_disorder": 14,
    "TLX3-related_condition": 1,
    "NPM1-related_disorder": 7,
    "not_provided|NPM1-related_disorder": 1,
    "not_specified|Acute_myeloid_leukemia|not_provided": 1,
    "NPM1-related_disorder|Myelodysplastic_syndrome_progressed_to_acute_myeloid_leukemia|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia_with_multilineage_dysplasia": 1,
    "not_specified|Neurodevelopmental|_jaw|_eye|_and_digital_syndrome|not_provided": 1,
    "Neurodevelopmental|_jaw|_eye|_and_digital_syndrome": 16,
    "Neurodevelopmental|_jaw|_eye|_and_digital_syndrome|not_provided": 3,
    "FBXW11-related_disorder|not_provided": 1,
    "not_provided|Neurodevelopmental|_jaw|_eye|_and_digital_syndrome": 2,
    "FBXW11-related_disorder": 6,
    "not_specified|Neurodevelopmental|_jaw|_eye|_and_digital_syndrome": 1,
    "not_provided|FBXW11-related_neurodevelopmental|_brain|_eye|_and_digit_anomalies|Neurodevelopmental|_jaw|_eye|_and_digital_syndrome": 1,
    "SH3PXD2B-related_disorder": 4,
    "Frank-Ter_Haar_syndrome": 147,
    "not_provided|Frank-Ter_Haar_syndrome": 26,
    "Frank-Ter_Haar_syndrome|not_provided": 18,
    "not_provided|Frank-Ter_Haar_syndrome|SH3PXD2B-related_disorder": 2,
    "SH3PXD2B-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Frank-Ter_Haar_syndrome": 2,
    "Frank-Ter_Haar_syndrome|SH3PXD2B-related_disorder|not_provided|not_specified": 1,
    "not_provided|Frank-Ter_Haar_syndrome|SH3PXD2B-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|SH3PXD2B-related_disorder|Frank-Ter_Haar_syndrome": 2,
    "Inborn_genetic_diseases|Frank-Ter_Haar_syndrome": 3,
    "not_provided|SH3PXD2B-related_disorder|Frank-Ter_Haar_syndrome|not_specified": 1,
    "SH3PXD2B-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|SH3PXD2B-related_disorder|Frank-Ter_Haar_syndrome": 1,
    "Frank-Ter_Haar_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "SH3PXD2B-related_disorder|not_provided|Frank-Ter_Haar_syndrome": 1,
    "not_provided|SH3PXD2B-related_disorder": 5,
    "Frank-Ter_Haar_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Frank-Ter_Haar_syndrome": 2,
    "not_provided|Frank-Ter_Haar_syndrome|not_specified": 2,
    "Frank-Ter_Haar_syndrome|not_specified|not_provided": 2,
    "not_provided|not_specified|Frank-Ter_Haar_syndrome": 3,
    "SH3PXD2B-related_disorder|Frank-Ter_Haar_syndrome|not_provided": 2,
    "not_provided|SH3PXD2B-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Frank-Ter_Haar_syndrome": 1,
    "Arthrogryposis_multiplex_congenita_2|_neurogenic_type": 3,
    "ERGIC1-related_disorder": 3,
    "not_provided|ERGIC1-related_disorder": 1,
    "SPONDYLOEPIPHYSEAL_DYSPLASIA|_HOLLING_TYPE|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Atrial_septal_defect_7": 272,
    "not_provided|Atrial_septal_defect_7|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Atrial_septal_defect_7": 52,
    "Cardiovascular_phenotype|not_provided|Atrial_septal_defect_7": 7,
    "Atrial_septal_defect_7|not_provided": 9,
    "Atrial_septal_defect_7|not_specified|not_provided": 1,
    "Atrial_septal_defect_7|Cardiovascular_phenotype": 47,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|not_provided": 4,
    "Atrioventricular_septal_defect|_somatic|Atrial_septal_defect_7": 1,
    "not_specified|Atrial_septal_defect_7|not_provided|Cardiovascular_phenotype|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Tetralogy_of_Fallot|Hypothyroidism|_congenital|_nongoitrous|_5": 1,
    "Atrial_septal_defect_7|Cardiovascular_phenotype|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|not_specified": 1,
    "Atrial_septal_defect_7|not_provided|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Tetralogy_of_Fallot": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrial_septal_defect_7|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Atrial_septal_defect_7|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Double_outlet_right_ventricle": 1,
    "not_provided|Atrial_septal_defect_7": 14,
    "Atrial_septal_defect_7|not_provided|Cardiovascular_phenotype": 4,
    "not_provided|Atrial_septal_defect_7|Cardiovascular_phenotype|not_specified": 1,
    "Atrial_septal_defect_7|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|Conotruncal_heart_malformations|Tetralogy_of_Fallot|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|Tetralogy_of_Fallot|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|not_provided": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|Hypothyroidism|_congenital|_nongoitrous|_5|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Tetralogy_of_Fallot": 1,
    "not_provided|Atrial_septal_defect_7|Cardiovascular_phenotype|NKX2-5-related_disorder": 1,
    "Conotruncal_heart_malformations|Atrial_septal_defect_7|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|not_provided|Cardiovascular_phenotype": 1,
    "Ventricular_septal_defect_3|Atrial_septal_defect_7": 1,
    "Atrial_septal_defect_7|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrial_septal_defect_7|not_specified|not_provided|Long_QT_syndrome|small_Atrial_septal_defect|Single_ventricle": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Atrial_septal_defect_7|Conotruncal_heart_malformations|Tetralogy_of_Fallot|not_provided|Malformation_of_the_heart_and_great_vessels|NKX2-5-related_disorder": 1,
    "Tetralogy_of_Fallot|Cardiovascular_phenotype|Atrial_septal_defect_7": 1,
    "Atrial_septal_defect_7|not_specified|Cardiovascular_phenotype": 2,
    "Atrial_septal_defect_7|Ventricular_septal_defect_3": 1,
    "Atrial_septal_defect_7|Cardiovascular_phenotype|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|not_provided": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Tetralogy_of_Fallot": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Atrial_septal_defect_7": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Atrial_septal_defect_7|NKX2-5-related_disorder|Cardiovascular_phenotype|Ventricular_septal_defect_3": 1,
    "not_provided|Atrial_septal_defect_7|Primary_dilated_cardiomyopathy|Atrial_septal_defect|Ventricular_fibrillation|Noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_isolated_congenital_asplenia|not_provided": 1,
    "Atrial_septal_defect_7|Cardiovascular_phenotype|not_provided": 2,
    "Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Atrial_septal_defect_7|Cardiovascular_phenotype": 1,
    "Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrial_septal_defect_7|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Cardiovascular_phenotype": 1,
    "Tetralogy_of_Fallot|not_provided|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Atrial_septal_defect_7": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_septal_defect_7|Tetralogy_of_Fallot": 1,
    "Atrial_septal_defect_7|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Atrial_septal_defect_7|not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "NKX2-5-related_disorder|Cardiovascular_phenotype|Atrial_septal_defect_7": 1,
    "not_provided|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrial_septal_defect_7|Cardiovascular_phenotype": 1,
    "NKX2-5-related_disorder|not_provided|Atrial_septal_defect_7|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|not_provided|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5": 1,
    "Cardiovascular_phenotype|NKX2-5-related_disorder|Atrial_septal_defect_7": 1,
    "Inborn_genetic_diseases|not_provided|Atrial_septal_defect_7": 1,
    "not_specified|Cardiovascular_phenotype|Atrial_septal_defect_7": 1,
    "not_provided|Atrial_septal_defect_7|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_septal_defect_7|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Abnormal_cardiovascular_system_morphology": 3,
    "Atrioventricular_septal_defect|_somatic": 1,
    "Ventricular_septal_defect_3": 3,
    "Cardiovascular_phenotype|not_provided|Atrial_septal_defect|not_specified|Atrial_septal_defect_7|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Atrial_septal_defect_7|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot": 1,
    "not_provided|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Atrial_septal_defect_7|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|NKX2-5-related_disorder|Atrial_septal_defect_7|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|not_specified": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_5|Atrial_septal_defect_7|not_provided": 1,
    "Malformation_of_the_heart_and_great_vessels": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_7|not_provided|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Tetralogy_of_Fallot|Congenital_heart_disease": 2,
    "Hypoplastic_left_heart_syndrome_2": 1,
    "Cardiovascular_phenotype|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Atrial_septal_defect_7": 1,
    "NKX2-5-related_disorder|not_provided|Atrial_septal_defect_7": 1,
    "Cardiovascular_phenotype|Tetralogy_of_Fallot|Atrial_septal_defect_7|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Atrial_septal_defect_7|Conotruncal_heart_malformations|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "NKX2-5-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Hypothyroidism|_congenital|_nongoitrous|_5|Atrial_septal_defect_7": 1,
    "not_specified|Atrial_septal_defect_7|Cardiovascular_phenotype": 2,
    "NKX2-5-related_disorder": 7,
    "NKX2-5-related_disorder|Atrial_septal_defect_7|Tetralogy_of_Fallot|Hypothyroidism|_congenital|_nongoitrous|_5|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|not_specified|not_provided": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_5": 1,
    "not_specified|Atrial_septal_defect_7": 2,
    "not_provided|Reclassified_-_variant_of_unknown_significance": 1,
    "NKX2-5-related_disorder|Atrial_septal_defect_7": 1,
    "Atrial_septal_defect_7|not_specified": 1,
    "Atrial_septal_defect_7|Cardiovascular_phenotype|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Atrial_septal_defect_7|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_septal_defect_7|NKX2-5-related_disorder|Hypothyroidism|_congenital|_nongoitrous|_5|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Atrial_septal_defect_7|Cardiovascular_phenotype|not_provided|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Atrial_septal_defect_7|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Atrial_septal_defect_7": 1,
    "Cardiovascular_phenotype|not_specified|Atrial_septal_defect_7": 1,
    "not_specified|Atrial_septal_defect_7|Conotruncal_heart_malformations|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Cardiovascular_phenotype": 1,
    "Conotruncal_heart_malformations|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Atrial_septal_defect_7|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Congenital_heart_disease|Aortic_arch_interruption|Hypoplastic_left_heart_syndrome_2|Atrial_septal_defect_7|Hypothyroidism|_congenital|_nongoitrous|_5|Tetralogy_of_Fallot|Persistent_truncus_arteriosus": 1,
    "Cardiovascular_phenotype|Abnormal_cardiovascular_system_morphology|not_provided|Atrial_septal_defect_7|not_specified": 1,
    "Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrial_septal_defect_7|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Congenital_heart_disease|Atrial_septal_defect_7|Tetralogy_of_Fallot": 1,
    "Tetralogy_of_Fallot|Hypothyroidism|_congenital|_nongoitrous|_5|Ventricular_septal_defect_3|Hypoplastic_left_heart_syndrome_2|Atrial_septal_defect_7|Conotruncal_heart_malformations|Cardiovascular_phenotype|not_specified": 1,
    "BOD1-related_disorder": 8,
    "BOD1-related_Intellectual_Disability": 1,
    "Parietal_foramina_1|Craniosynostosis_2": 41,
    "Craniosynostosis_2|Parietal_foramina_1": 9,
    "not_provided|Parietal_foramina_1|Craniosynostosis_2": 1,
    "Cranium_bifidum_occultum": 92,
    "Cranium_bifidum_occultum|MSX2-related_disorder": 2,
    "Craniosynostosis_2": 5,
    "MSX2-related_disorder|Cranium_bifidum_occultum": 2,
    "Inborn_genetic_diseases|Cranium_bifidum_occultum": 8,
    "Cranium_bifidum_occultum|not_specified": 1,
    "Cranium_bifidum_occultum|Inborn_genetic_diseases": 4,
    "not_provided|MSX2-related_disorder|Inborn_genetic_diseases": 1,
    "Cranium_bifidum_occultum|not_provided": 3,
    "Parietal_foramina_1": 5,
    "Craniosynostosis_2|Parietal_foramina_1|not_specified|Cranium_bifidum_occultum": 1,
    "not_provided|Parietal_foramina_1": 1,
    "Craniosynostosis_2|Parietal_foramina_with_cleidocranial_dysplasia|Parietal_foramina_1": 1,
    "Cranium_bifidum_occultum|not_provided|not_specified|Craniosynostosis_2|Parietal_foramina_1": 1,
    "Craniosynostosis_2|Cranium_bifidum_occultum": 1,
    "Cranium_bifidum_occultum|Craniosynostosis_2": 2,
    "Parietal_foramina_with_cleidocranial_dysplasia": 1,
    "MSX2-related_disorder": 3,
    "Inborn_genetic_diseases|Craniosynostosis_2|Parietal_foramina_1": 1,
    "not_provided|Cranium_bifidum_occultum": 1,
    "Parietal_foramina_1|MSX2-related_disorder|Cranium_bifidum_occultum|Craniosynostosis_2": 1,
    "Craniosynostosis_2|Parietal_foramina_1|Inborn_genetic_diseases|Cranium_bifidum_occultum": 1,
    "not_provided|Craniosynostosis_2|Parietal_foramina_1": 1,
    "Parietal_foramina_1|not_provided|Craniosynostosis_2": 1,
    "Cranium_bifidum_occultum|Craniosynostosis_syndrome": 2,
    "DRD1-related_Dystonia": 1,
    "SNCB-related_disorder": 1,
    "Lewy_body_dementia|SNCB-related_disorder|not_provided": 1,
    "Lewy_body_dementia|not_specified|not_provided": 1,
    "UNC5A-related_disorder": 2,
    "FGFR4-related_disorder|not_provided": 1,
    "FGFR4-related_disorder": 12,
    "Classic_Hodgkin_lymphoma|FGFR4-related_disorder": 1,
    "Cancer_progression_and_tumor_cell_motility|See_cases|FGFR4-related_disorder|not_specified": 1,
    "Sotos_syndrome": 443,
    "not_specified|Sotos_syndrome|NSD1-related_disorder": 1,
    "not_provided|Sotos_syndrome": 101,
    "Inborn_genetic_diseases|not_provided|Sotos_syndrome": 9,
    "Sotos_syndrome|not_specified|not_provided": 6,
    "NSD1-related_disorder": 29,
    "Sotos_syndrome|not_provided": 111,
    "not_provided|Inborn_genetic_diseases|Sotos_syndrome": 8,
    "not_specified|Sotos_syndrome|Inborn_genetic_diseases|not_provided|NSD1-related_disorder": 1,
    "not_provided|NSD1-related_disorder|Sotos_syndrome": 2,
    "not_provided|Beckwith-Wiedemann_syndrome": 31,
    "Inborn_genetic_diseases|Sotos_syndrome|not_provided": 10,
    "Inborn_genetic_diseases|not_provided|not_specified|Sotos_syndrome": 2,
    "NSD1-related_disorder|not_provided": 12,
    "NSD1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|NSD1-related_disorder|not_provided": 2,
    "not_specified|NSD1-related_disorder|Sotos_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NSD1-related_disorder": 3,
    "not_provided|Sotos_syndrome|NSD1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Sotos_syndrome": 10,
    "Sotos_syndrome|not_provided|Inborn_genetic_diseases": 8,
    "Sotos_syndrome|Inborn_genetic_diseases|NSD1-related_disorder|not_specified|not_provided": 2,
    "not_provided|NSD1-related_disorder|Sotos_syndrome|Intellectual_disability": 1,
    "Beckwith-Wiedemann_syndrome|Sotos_syndrome": 11,
    "not_provided|NSD1-related_disorder": 13,
    "not_provided|Weaver_syndrome|Sotos_syndrome": 3,
    "not_provided|Sotos_syndrome|Inborn_genetic_diseases": 10,
    "Sotos_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 14,
    "not_provided|Sotos_syndrome|NSD1-related_disorder": 1,
    "Sotos_syndrome|not_provided|not_specified": 4,
    "Inborn_genetic_diseases|Sotos_syndrome|NSD1-related_disorder|not_specified|not_provided": 2,
    "Sotos_syndrome|NSD1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Sotos_syndrome|not_provided|Acute_myeloid_leukemia|Inborn_genetic_diseases": 1,
    "Sotos_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 7,
    "Sotos_syndrome|Inborn_genetic_diseases|not_provided": 8,
    "not_provided|Sotos_syndrome|Inborn_genetic_diseases|not_specified": 2,
    "NSD1-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Sotos_syndrome|Inborn_genetic_diseases": 5,
    "not_specified|not_provided|Inborn_genetic_diseases|Sotos_syndrome": 2,
    "not_provided|not_specified|Sotos_syndrome|Inborn_genetic_diseases": 1,
    "Beckwith-Wiedemann_syndrome": 972,
    "Sotos_syndrome|Acute_myeloid_leukemia": 3,
    "not_specified|Sotos_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Sotos_syndrome|not_specified|not_provided": 3,
    "Acute_myeloid_leukemia|Sotos_syndrome|not_provided": 1,
    "Sotos_syndrome|Inborn_genetic_diseases|not_provided|NSD1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Sotos_syndrome|not_provided": 2,
    "Sotos_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome|NSD1-related_disorder|Sotos_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|NSD1-related_disorder|Sotos_syndrome": 1,
    "Sotos_syndrome|Beckwith-Wiedemann_syndrome": 5,
    "not_provided|NSD1-related_disorder|Inborn_genetic_diseases|Sotos_syndrome|not_specified": 1,
    "Sotos_syndrome|not_provided|Acute_myeloid_leukemia": 1,
    "not_specified|Sotos_syndrome": 1,
    "not_provided|NSD1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Sotos_syndrome|not_provided|not_specified": 2,
    "not_provided|Neurodevelopmental_delay": 4,
    "Inborn_genetic_diseases|not_specified|not_provided|Sotos_syndrome": 3,
    "not_provided|Sotos_syndrome|Beckwith-Wiedemann_syndrome": 3,
    "Congenital_diaphragamitc_hernia": 1,
    "Sotos_syndrome|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "not_specified|Sotos_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|NSD1-related_disorder|Sotos_syndrome|Inborn_genetic_diseases": 3,
    "Sotos_syndrome|not_provided|NSD1-related_disorder": 1,
    "Sotos_syndrome|NSD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Sotos_syndrome|NSD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Sotos_syndrome": 1,
    "not_specified|not_provided|Sotos_syndrome": 6,
    "not_provided|Sotos_syndrome|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|Sotos_syndrome|NSD1-related_disorder|not_provided": 1,
    "Weaver_syndrome|not_provided|NSD1-related_disorder|Sotos_syndrome": 1,
    "Beckwith-Wiedemann_syndrome|not_provided|Sotos_syndrome": 1,
    "Sotos_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Weaver_syndrome": 1,
    "NSD1-related_disorder|Sotos_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "NSD1-related_disorder|not_provided|not_specified": 1,
    "NSD1-related_disorder|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|NSD1-related_disorder|Sotos_syndrome": 1,
    "not_provided|Sotos_syndrome|not_specified": 1,
    "NSD1-related_disorder|Sotos_syndrome|not_provided": 3,
    "NSD1-related_disorder|Sotos_syndrome|not_provided|not_specified": 1,
    "NSD1-related_disorder|not_provided|Sotos_syndrome|Inborn_genetic_diseases": 1,
    "Sotos_syndrome|NSD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Weaver_syndrome": 1,
    "not_provided|NSD1-related_disorder|Sotos_syndrome|not_specified": 1,
    "Sotos_syndrome|Inborn_genetic_diseases|NSD1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|NSD1-related_disorder|not_provided": 1,
    "See_cases|Sotos_syndrome": 1,
    "Acute_myeloid_leukemia|Sotos_syndrome|not_provided|Neurodevelopmental_delay": 1,
    "Sotos_syndrome|NSD1-related_disorder|not_provided": 2,
    "Sotos_syndrome|Inborn_genetic_diseases|See_cases": 1,
    "not_provided|Marfanoid_habitus_and_intellectual_disability|Sotos_syndrome": 1,
    "not_provided|Increased_body_weight|Preeclampsia|Macrocephaly|High_forehead|Osteopenia|Overgrowth|Pointed_chin|Delayed_speech_and_language_development|Tall_stature|High_anterior_hairline|Global_developmental_delay|Delayed_gross_motor_development|Hypoplasia_of_the_corpus_callosum|Scoliosis|Hypertelorism|Sotos_syndrome": 1,
    "Sotos_syndrome|not_specified|not_provided|See_cases": 1,
    "Sotos_syndrome|NSD1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder|Sotos_syndrome": 1,
    "Inborn_genetic_diseases|NSD1-related_disorder|Sotos_syndrome|not_provided": 1,
    "Hereditary_cancer|Inborn_genetic_diseases|Sotos_syndrome|NSD1-related_disorder|not_provided": 1,
    "Choroid_plexus_carcinoma": 3,
    "Inborn_genetic_diseases|NSD1-related_disorder|Sotos_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Sotos_syndrome|Beckwith-Wiedemann_syndrome|not_specified|not_provided": 1,
    "Sotos_syndrome|not_specified": 1,
    "Hereditary_spastic_paraplegia_8": 47,
    "Weaver_syndrome|Sotos_syndrome": 9,
    "Sotos_syndrome|Weaver_syndrome": 2,
    "Weaver_syndrome|Sotos_syndrome|not_provided": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1": 32,
    "Prostate_cancer|Inborn_genetic_diseases": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2": 56,
    "Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Hypercalcemia|_infantile|_2|Inborn_genetic_diseases|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1": 1,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2": 10,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|not_provided": 9,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1": 3,
    "not_provided|Inborn_genetic_diseases|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2": 1,
    "Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2": 3,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 5,
    "Inborn_genetic_diseases|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2": 1,
    "SLC34A1-related_disorder|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 1,
    "Hypercalcemia|_infantile|_2|not_provided|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 3,
    "Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Inborn_genetic_diseases": 2,
    "Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 3,
    "Inborn_genetic_diseases|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|SLC34A1-related_disorder": 1,
    "SLC34A1-related_disorder|not_specified|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Decreased_total_lymphocyte_count|Decreased_total_neutrophil_count": 1,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2": 4,
    "Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Inborn_genetic_diseases": 1,
    "SLC34A1-related_disorder": 6,
    "not_provided|not_specified|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|not_provided": 9,
    "not_provided|SLC34A1-related_disorder|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Nephrocalcinosis": 1,
    "Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|not_provided": 2,
    "Hypercalcemia|_infantile|_2|not_provided": 6,
    "Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 1,
    "Hypercalcemia|_infantile|_2|SLC34A1-related_disorder|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|not_provided": 2,
    "not_provided|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2": 4,
    "not_provided|Hypercalcemia|_infantile|_2": 3,
    "Hypercalcemia|_infantile|_2": 12,
    "Nephrocalcinosis|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 1,
    "Inborn_genetic_diseases|SLC34A1-related_disorder|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|not_provided": 1,
    "not_provided|SLC34A1-related_disorder": 4,
    "not_provided|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2": 1,
    "Nephrocalcinosis|Nephrolithiasis|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|SLC34A1-related_disorder|not_provided": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|SLC34A1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Fanconi_renotubular_syndrome_2": 2,
    "Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Autosomal_recessive_infantile_hypercalcemia|not_provided": 1,
    "Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|not_specified|not_provided": 1,
    "Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|SLC34A1-related_disorder": 1,
    "SLC34A1-related_disorder|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|not_specified|not_provided": 1,
    "Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2": 1,
    "Inborn_genetic_diseases|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 1,
    "Inborn_genetic_diseases|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2": 1,
    "not_provided|Inborn_genetic_diseases|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2": 1,
    "Fanconi_renotubular_syndrome_2": 2,
    "not_provided|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1": 1,
    "not_provided|SLC34A1-related_disorder|Hypercalcemia|_infantile|_2": 1,
    "Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|not_provided": 4,
    "not_provided|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1": 4,
    "Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|SLC34A1-related_disorder|Nephrocalcinosis|Nephrolithiasis|not_provided": 1,
    "SLC34A1-related_disorder|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided": 1,
    "Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided|Inborn_genetic_diseases": 2,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|SLC34A1-related_disorder": 1,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2": 1,
    "SLC34A1-related_disorder|not_provided": 2,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|not_specified|not_provided": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|not_provided|Fanconi_renotubular_syndrome_2": 1,
    "Factor_XII_deficiency_disease|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Nephrolithiasis/osteoporosis|_hypophosphatemic|Hereditary_angioneurotic_edema|not_provided": 2,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Fanconi_renotubular_syndrome_2": 1,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Hypercalcemia|_infantile|_2|Inborn_genetic_diseases": 1,
    "not_specified|Hypophosphatemic_nephrolithiasis/osteoporosis_1|not_provided|Factor_XII_deficiency_disease|Hereditary_angioneurotic_edema|Nephrolithiasis/osteoporosis|_hypophosphatemic": 1,
    "SLC34A1-related_disorder|Nephrocalcinosis|not_provided": 1,
    "Factor_XII_deficiency_disease|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Nephrolithiasis/osteoporosis|_hypophosphatemic|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hereditary_angioneurotic_edema": 1,
    "Nephrolithiasis|Nephrocalcinosis|Hypercalcemia|_infantile|_2|Fanconi_renotubular_syndrome_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|SLC34A1-related_disorder|not_provided": 1,
    "Fanconi_renotubular_syndrome_2|Hypercalcemia|_infantile|_2|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Inborn_genetic_diseases|not_provided": 1,
    "Factor_XII_deficiency_disease|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Nephrolithiasis/osteoporosis|_hypophosphatemic|Hereditary_angioneurotic_edema": 3,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_1|Nephrolithiasis/osteoporosis|_hypophosphatemic": 1,
    "Factor_XII_deficiency_disease|Hypophosphatemic_nephrolithiasis/osteoporosis_1|Nephrolithiasis/osteoporosis|_hypophosphatemic|Hereditary_angioneurotic_edema": 1,
    "Factor_XII_deficiency_disease|Hereditary_angioedema_type_3": 6,
    "Hereditary_angioedema_type_3": 6,
    "FACTOR_XII_(WASHINGTON_D.C.)": 1,
    "Factor_XII_deficiency_disease": 10,
    "F12-related_disorder|not_provided|Hereditary_angioedema_type_3|Factor_XII_deficiency_disease": 1,
    "Factor_XII_deficiency_disease|Hereditary_angioedema_type_3|not_provided": 4,
    "Hereditary_angioedema_type_3|F12-related_disorder|Nephrolithiasis/osteoporosis|_hypophosphatemic|Factor_XII_deficiency_disease|Hereditary_angioneurotic_edema|not_provided": 1,
    "Nephrolithiasis/osteoporosis|_hypophosphatemic|F12-related_disorder|Hereditary_angioneurotic_edema|not_provided|Factor_XII_deficiency_disease|Hereditary_angioedema_type_3": 1,
    "Hereditary_angioedema_type_3|Nephrolithiasis/osteoporosis|_hypophosphatemic|F12-related_disorder|Factor_XII_deficiency_disease|Hereditary_angioneurotic_edema|not_provided": 1,
    "not_provided|F12-related_disorder": 2,
    "F12-related_disorder": 7,
    "Hereditary_angioedema_type_3|Nephrolithiasis/osteoporosis|_hypophosphatemic|Factor_XII_deficiency_disease|Hereditary_angioneurotic_edema": 1,
    "not_specified|Hereditary_angioneurotic_edema|not_provided|Nephrolithiasis/osteoporosis|_hypophosphatemic|Factor_XII_deficiency_disease|Hereditary_angioedema_type_3": 1,
    "Hereditary_angioedema_type_3|Factor_XII_deficiency_disease|F12-related_disorder": 1,
    "Hereditary_angioedema_type_3|Factor_XII_deficiency_disease": 9,
    "F12-related_disorder|not_provided": 2,
    "FACTOR_XII_(LOCARNO)": 1,
    "not_provided|Hereditary_angioedema_type_3|Factor_XII_deficiency_disease": 3,
    "Factor_XII_deficiency_disease|Inborn_genetic_diseases": 1,
    "F12-related_disorder|not_specified|not_provided|Factor_XII_deficiency_disease": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_angioedema_type_3|Factor_XII_deficiency_disease": 1,
    "Hereditary_angioedema_type_3|not_provided": 3,
    "Hereditary_angioedema_type_3|F12-related_disorder": 1,
    "Hereditary_angioedema_type_3|Factor_XII_deficiency_disease|not_provided": 6,
    "Hereditary_angioedema_type_3|Factor_XII_deficiency_disease|Angioedema|Hyperbilirubinemia|Urticaria|Hypertensive_disorder": 1,
    "Hereditary_angioneurotic_edema|Hereditary_angioedema_type_3|Factor_XII_deficiency_disease|not_provided": 1,
    "not_specified|Factor_XII_deficiency_disease|Hereditary_angioedema_type_3|not_provided": 1,
    "not_provided|F12-related_disorder|Factor_XII_deficiency_disease|Hereditary_angioedema_type_3": 1,
    "Inborn_genetic_diseases|Factor_XII_deficiency_disease|not_provided": 1,
    "Factor_XII_deficiency_disease|Hereditary_angioedema_type_3|Inborn_genetic_diseases": 1,
    "F12-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|F12-related_disorder": 1,
    "not_provided|Hereditary_angioedema_type_3|F12-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|F12_POLYMORPHISM|Hereditary_angioedema_type_3|Factor_XII_deficiency_disease|not_provided": 1,
    "F12-related_disorder|not_provided|Hereditary_angioedema_type_3|Factor_XII_deficiency_disease|Hereditary_angioneurotic_edema": 1,
    "Hereditary_angioneurotic_edema|Factor_XII_deficiency_disease|Hereditary_angioedema_type_3|not_provided": 1,
    "DDX41-related_disorder|not_specified|not_provided": 1,
    "DDX41-related_disorder": 13,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases": 19,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|not_provided|DDX41-related_disorder": 1,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome": 60,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 19,
    "Inborn_genetic_diseases|DDX41-related_disorder": 6,
    "not_provided|Inborn_genetic_diseases|DDX41-related_disorder": 2,
    "not_provided|not_specified|DDX41-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|DDX41-related_hematologic_malignancy_predisposition_syndrome": 12,
    "not_provided|DDX41-related_hematologic_malignancy_predisposition_syndrome": 8,
    "Myelodysplastic_syndrome|Inborn_genetic_diseases|DDX41-related_hematologic_malignancy_predisposition_syndrome": 1,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases|DDX41-related_disorder|not_provided": 1,
    "Acute_myeloid_leukemia|DDX41-related_hematologic_malignancy_predisposition_syndrome|not_provided|DDX41-related_disorder|Inborn_genetic_diseases": 1,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|not_provided": 7,
    "DDX41-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|DDX41-related_hematologic_malignancy_predisposition_syndrome": 1,
    "DDX41-related_disorder|DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|DDX41-related_hematologic_malignancy_predisposition_syndrome|DDX41-related_disorder": 1,
    "DDX41-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|DDX41-related_disorder|Inborn_genetic_diseases|not_specified": 2,
    "not_provided|DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases": 31,
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    "Bone_marrow_hypocellularity|not_provided|DDX41-related_hematologic_malignancy_predisposition_syndrome|Inborn_genetic_diseases": 1,
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    "DDX41-related_disorder|Inborn_genetic_diseases|Myelodysplasia|DDX41-related_hematologic_malignancy_predisposition_syndrome|not_provided|Bone_marrow_hypocellularity": 1,
    "Ehlers-Danlos_syndrome_progeroid_type|not_provided": 1,
    ".|Inborn_genetic_diseases": 57,
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    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_progeroid_type|not_specified": 1,
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    "not_provided|Ehlers-Danlos_syndrome_progeroid_type": 9,
    ".|Ehlers-Danlos_syndrome_progeroid_type|not_specified": 1,
    "not_provided|.": 104,
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    "Ehlers-Danlos_syndrome_progeroid_type|Inborn_genetic_diseases|not_provided": 2,
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    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_progeroid_type": 1,
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    "Inborn_genetic_diseases|.": 53,
    "not_specified|.|Inborn_genetic_diseases|not_provided": 2,
    "Ehlers-Danlos_syndrome|.": 2,
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    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|.": 1,
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    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|.|not_specified|not_provided|Ehlers-Danlos_syndrome_progeroid_type": 1,
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    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|not_provided|.|Spondylodysplastic_Ehlers-Danlos_syndrome|Inborn_genetic_diseases": 1,
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    "Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|.|Inborn_genetic_diseases|not_provided": 1,
    ".|Lethal_skeletal_dysplasia|Ehlers-Danlos_syndrome|_spondylodysplastic_type|_1|not_provided|Larsen-like_syndrome|_B3GAT3_type|Ehlers-Danlos_syndrome_progeroid_type": 1,
    ".|not_provided|Ehlers-Danlos_syndrome|B4GALT7-related_disorder": 1,
    "not_provided|Ehlers-Danlos_syndrome_progeroid_type|Inborn_genetic_diseases|not_specified": 1,
    ".|not_provided|not_specified": 4,
    ".|B4GALT7-related_disorder": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_progeroid_type": 1,
    ".|not_specified|not_provided": 6,
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    "not_provided|Pituitary_hormone_deficiency|_combined|_2": 15,
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    "Pituitary_hormone_deficiency|_combined|_2|not_provided": 25,
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    "Pituitary_hormone_deficiency|_combined|_2|PROP1-related_disorder|not_provided": 2,
    "Pituitary_hormone_deficiency|_combined|_2|not_specified|not_provided|Amenorrhea": 1,
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    "Pituitary_hormone_deficiency|_combined|_2|Inborn_genetic_diseases|PROP1-related_disorder|not_provided": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|Pituitary_hormone_deficiency|_combined|_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_2": 1,
    "46|XY_partial_gonadal_dysgenesis|PROP1-related_disorder|not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form|Pituitary_hormone_deficiency|_combined|_2": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided|Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_2": 1,
    "not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form|Pituitary_hormone_deficiency|_combined|_2": 1,
    "not_provided|Pituitary_hormone_deficiency|_combined|_2|not_specified": 3,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided|Pituitary_hormone_deficiency|_combined|_2|See_cases": 1,
    "not_specified|not_provided|Pituitary_hormone_deficiency|_combined|_2": 1,
    "Pituitary_hormone_deficiency|_combined|_2|not_specified|not_provided": 1,
    "not_specified|Pituitary_hormone_deficiency|_combined|_2|not_provided": 1,
    "PROP1-related_disorder|Combined_pituitary_hormone_deficiencies|_genetic_form|Pituitary_hormone_deficiency|_combined|_2|not_provided": 1,
    "not_provided|Pituitary_hormone_deficiency|_combined|_2|Inborn_genetic_diseases": 1,
    "NHP2-related_disorder": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_2|Dyskeratosis_congenita|_autosomal_recessive_1": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_2": 5,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_2": 3,
    "Dyskeratosis_congenita|_autosomal_recessive_1|Dyskeratosis_congenita|_autosomal_recessive_2": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_2|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|not_specified|NHP2-related_disorder": 1,
    "not_specified|Dyskeratosis_congenita|not_provided|NHP2-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_2|Dyskeratosis_congenita|_autosomal_recessive_1|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_1|Dyskeratosis_congenita|_autosomal_recessive_2": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_2|Dyskeratosis_congenita": 2,
    "NHP2-related_disorder|not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_2|Dyskeratosis_congenita": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_2": 1,
    "Dyskeratosis_congenita|Dyskeratosis_Congenita|_Recessive": 1,
    "NHP2-related_disorder|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|NHP2-related_disorder": 1,
    "not_provided|Dyskeratosis_congenita|not_specified|Dyskeratosis_congenita|_autosomal_recessive_2": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_2|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|not_specified": 16,
    "NHP2-related_disorder|not_provided|Dyskeratosis_congenita|not_specified|Dyskeratosis_congenita|_autosomal_recessive_2": 1,
    "Dyskeratosis_congenita|not_specified|not_provided": 6,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_2": 1,
    "Phosphohydroxylysinuria": 2,
    "PHYKPL-related_disorder": 7,
    "not_provided|GRM6-related_disorder": 14,
    "Congenital_stationary_night_blindness_1B": 9,
    "Congenital_stationary_night_blindness_1B|not_provided": 7,
    "GRM6-related_disorder|not_provided": 11,
    "GRM6-related_disorder": 3,
    "not_provided|Congenital_stationary_night_blindness_1B": 5,
    "not_provided|Congenital_stationary_night_blindness|Congenital_stationary_night_blindness_1B": 1,
    "Congenital_stationary_night_blindness_1B|not_provided|Retinal_dystrophy": 1,
    "Congenital_stationary_night_blindness_1B|not_provided|not_specified": 1,
    "GRM6-related_disorder|not_specified|not_provided": 2,
    "not_provided|not_specified|Congenital_stationary_night_blindness_1B|GRM6-related_disorder": 1,
    "Congenital_stationary_night_blindness_1B|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Congenital_stationary_night_blindness_1B|Retinal_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_stationary_night_blindness_1B": 1,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1B": 4,
    "not_provided|Congenital_stationary_night_blindness_1B|not_specified": 1,
    "Congenital_stationary_night_blindness_1B|not_specified|not_provided": 2,
    "GRM6-related_disorder|not_provided|Congenital_stationary_night_blindness_1B": 1,
    "GRM6-related_disorder|not_specified|not_provided|Congenital_stationary_night_blindness_1B": 1,
    "Congenital_stationary_night_blindness|Congenital_stationary_night_blindness_1B": 1,
    "GRM6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_stationary_night_blindness_1B|not_provided|Congenital_stationary_night_blindness": 1,
    "Inborn_genetic_diseases|Optic_atrophy|not_provided": 3,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1318,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 68,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 51,
    "ADAMTS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 8,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 32,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 7,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified": 28,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified": 9,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|not_specified": 1,
    "ADAMTS2-related_disorder|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 4,
    "not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 7,
    "not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 29,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases|not_specified": 3,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|not_provided": 6,
    "not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases": 20,
    "not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases": 2,
    "ADAMTS2-related_disorder|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 2,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 3,
    "not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 2,
    "ADAMTS2-related_disorder|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 4,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided|not_specified": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder": 1,
    "ADAMTS2-related_disorder|not_provided|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|See_cases|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 2,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Ehlers-Danlos_syndrome|not_provided": 2,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 5,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder": 3,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 5,
    "See_cases|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder|not_provided": 5,
    "not_provided|Ehlers-Danlos_syndrome|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 2,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Ehlers-Danlos_syndrome": 7,
    "not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 6,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 2,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|ADAMTS2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 3,
    "ADAMTS2-related_disorder": 4,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified": 4,
    "Inborn_genetic_diseases|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|ADAMTS2-related_disorder|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "not_provided|ADAMTS2-related_disorder|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder": 4,
    "not_specified|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "not_provided|ADAMTS2-related_disorder": 1,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases|not_specified": 1,
    "Ehlers-Danlos_syndrome|Inborn_genetic_diseases|not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided|ADAMTS2-related_disorder|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Ehlers-Danlos_syndrome": 1,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|ADAMTS2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|ADAMTS2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_dermatosparaxis_type|ADAMTS2-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|not_specified|Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Ehlers-Danlos_syndrome|not_provided": 1,
    "not_provided|ADAMTS2-related_disorder|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_dermatosparaxis_type|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "ADAMTS2-related_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type|Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome|Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|_dermatosparaxis_type": 1,
    "Neurodevelopmental_disorder_with_craniofacial_dysmorphism_and_skeletal_defects": 6,
    "Neurodevelopmental_disorder_with_craniofacial_dysmorphism_and_skeletal_defects|not_provided": 1,
    "HNRNPH1-related_disorder": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_craniofacial_dysmorphism_and_skeletal_defects|not_provided": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Bain_type": 8,
    "Hypotonia-failure_to_thrive-microcephaly_syndrome": 1,
    "Asthma|_nasal_polyps|_and_aspirin_intolerance": 1,
    "Bone_Paget_disease|not_provided": 3,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3": 5,
    "Paget_disease_of_bone_3": 37,
    "SQSTM1-related_disorder": 11,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 10,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 206,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 261,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 8,
    "SQSTM1-related_disorder|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_3|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 16,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3": 4,
    "SQSTM1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 12,
    "Inborn_genetic_diseases|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 4,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided": 17,
    "Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset|Myopathy|_distal|_with_rimmed_vacuoles": 1,
    "not_provided|not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Inborn_genetic_diseases": 1,
    "SQSTM1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 7,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder|not_provided": 5,
    "SQSTM1-related_disorder|not_provided|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 2,
    "not_provided|Paget_disease_of_bone_3": 6,
    "SQSTM1-related_disorder|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 9,
    "not_provided|Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Inborn_genetic_diseases": 7,
    "Myopathy|_distal|_with_rimmed_vacuoles|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_specified": 1,
    "Myopathy|_distal|_with_rimmed_vacuoles|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder": 11,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|SQSTM1-related_disorder": 7,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 2,
    "Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset|Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Myopathy|_distal|_with_rimmed_vacuoles": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Inborn_genetic_diseases|not_provided": 1,
    "Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 4,
    "Neurodegeneration_with_ataxia|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided|Paget_disease_of_bone_3": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_provided": 8,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3|not_specified|not_provided": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|SQSTM1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder": 1,
    "SQSTM1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided": 3,
    "Myopathy|_distal|_with_rimmed_vacuoles|not_provided|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Paget_disease_of_bone_3|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Myopathy|_distal|_with_rimmed_vacuoles|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_specified|SQSTM1-related_disorder|not_provided": 1,
    "Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder": 1,
    "Paget_disease_of_bone_3|SQSTM1-related_disorder|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder": 2,
    "Amyotrophic_lateral_sclerosis|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|not_provided|SQSTM1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3|SQSTM1-related_disorder": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Inborn_genetic_diseases": 4,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_3|not_specified|not_provided": 1,
    "Myopathy|_distal|_with_rimmed_vacuoles|not_provided|Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis": 1,
    "not_provided|SQSTM1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "not_provided|Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Inborn_genetic_diseases|SQSTM1-related_disorder": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided|SQSTM1-related_disorder|Paget_disease_of_bone_3": 1,
    "not_provided|See_cases|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Myopathy|_distal|_with_rimmed_vacuoles|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided": 2,
    "not_specified|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_provided|Paget_disease_of_bone_3": 1,
    "not_specified|Myopathy|_distal|_with_rimmed_vacuoles|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "not_provided|Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_specified|not_provided|Paget_disease_of_bone_3": 1,
    "not_specified|not_provided|SQSTM1-related_disorder|Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "See_cases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided|SQSTM1-related_disorder|Paget_disease_of_bone_3": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Myopathy|_distal|_with_rimmed_vacuoles|not_provided": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_specified|Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset|Myopathy|_distal|_with_rimmed_vacuoles|not_provided": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|SQSTM1-related_disorder|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_specified|Paget_disease_of_bone_3": 1,
    "See_cases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "not_provided|not_specified|Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "SQSTM1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_specified|Paget_disease_of_bone_3|not_provided": 1,
    "SQSTM1-related_disorder|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "SQSTM1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Myopathy|_distal|_with_rimmed_vacuoles|Paget_disease_of_bone_3": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Inborn_genetic_diseases|SQSTM1-related_disorder": 1,
    "Spastic_paraplegia-Paget_disease_of_bone_syndrome|Bone_Paget_disease|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_3|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "not_specified|not_provided|Paget_disease_of_bone_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Myopathy|_distal|_with_rimmed_vacuoles|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|not_provided": 1,
    "not_specified|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_3|Myopathy|_distal|_with_rimmed_vacuoles|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|SQSTM1-related_disorder|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Paget_disease_of_bone_3|not_provided": 1,
    "not_provided|SQSTM1-related_disorder|Paget_disease_of_bone_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset|Neurodegeneration_with_ataxia|_dystonia|_and_gaze_palsy|_childhood-onset": 1,
    "SQSTM1-related_disorder|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|Paget_disease_of_bone_2|_early-onset": 1,
    "SQSTM1-related_disorder|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_provided": 1,
    "not_provided|Paget_disease_of_bone_3|not_specified|Paget_disease_of_bone_2|_early-onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 1,
    "Paget_disease_of_bone_3|not_provided": 1,
    "Paget_disease_of_bone_3|not_specified": 1,
    "Bone_Paget_disease": 1,
    "GFPT2-related_disorder": 1,
    "FLT4-related_disorder|not_provided": 2,
    "FLT4-related_disorder": 50,
    "Hereditary_lymphedema_type_I": 31,
    "Hereditary_lymphedema_type_I|Inborn_genetic_diseases": 2,
    "Congenital_heart_defects|_multiple_types|_7": 18,
    "not_provided|FLT4-related_disorder": 4,
    "Capillary_infantile_hemangioma|Congenital_heart_defects|_multiple_types|_7|Hereditary_lymphedema_type_I|Inborn_genetic_diseases": 1,
    "Capillary_infantile_hemangioma|Congenital_heart_defects|_multiple_types|_7|Hereditary_lymphedema_type_I": 2,
    "Blepharospasm-oromandibular_dystonia_syndrome": 1,
    "Capillary_infantile_hemangioma|Hereditary_lymphedema_type_I|Congenital_heart_defects|_multiple_types|_7|FLT4-related_disorder|not_provided": 1,
    "Hereditary_lymphedema_type_I|not_provided": 5,
    "Hereditary_lymphedema_type_I|FLT4-related_disorder": 2,
    "Hereditary_lymphedema_type_I|not_provided|not_specified|Congenital_heart_defects|_multiple_types|_7": 2,
    "not_specified|Congenital_heart_defects|_multiple_types|_7|Hereditary_lymphedema_type_I|not_provided": 1,
    "not_provided|Capillary_infantile_hemangioma|Congenital_heart_defects|_multiple_types|_7|Hereditary_lymphedema_type_I": 1,
    "not_provided|Hereditary_lymphedema_type_I|FLT4-related_disorder": 1,
    "not_provided|Hereditary_lymphedema_type_I": 3,
    "not_provided|Hereditary_lymphedema_type_I|Non-immune_hydrops_fetalis|FLT4-related_disorder": 1,
    "FLT4-related_disorder|not_provided|Hereditary_lymphedema_type_I": 1,
    "Inborn_genetic_diseases|FLT4-related_disorder|not_provided": 1,
    "Capillary_infantile_hemangioma|Colorectal_cancer|not_provided|not_specified": 1,
    "not_provided|Hereditary_lymphedema_type_I|Congenital_heart_defects|_multiple_types|_7|not_specified": 1,
    "Hereditary_lymphedema_type_I|not_specified|Congenital_heart_defects|_multiple_types|_7|not_provided": 2,
    "not_specified|Hereditary_lymphedema_type_I|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_7|Hereditary_lymphedema_type_I|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_lymphedema_type_I|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|not_specified|not_provided": 1,
    "Hereditary_lymphedema_type_I|Congenital_heart_defects|_multiple_types|_7|not_specified": 1,
    "not_specified|Congenital_heart_defects|_multiple_types|_7|not_provided|Hereditary_lymphedema_type_I": 1,
    "Inborn_genetic_diseases|Hereditary_lymphedema_type_I": 1,
    "FLT4-related_disorder|Hereditary_lymphedema_type_I": 1,
    "Lymphedema|not_provided": 2,
    "FLT4-related_disorder|not_specified|not_provided": 1,
    "Regorafenib_response": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_7": 1,
    "Congenital_heart_defects|_multiple_types|_7|Hereditary_lymphedema_type_I|Capillary_infantile_hemangioma": 1,
    "Congenital_heart_defects|_multiple_types|_7|not_provided": 1,
    "DUSP22-related_disorder": 20,
    "DUSP22-related_disorder|not_specified": 1,
    "Immunodeficiency_131": 2,
    "IRF4-related_disorder|not_specified": 1,
    "not_provided|Immunodeficiency_131": 1,
    "not_provided|IRF4-related_disorder": 5,
    "Skin/hair/eye_pigmentation|_variation_in|_8": 2,
    "IRF4-related_disorder|not_provided": 2,
    "Immunodeficiency_131|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 26,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_cerebellar_hypoplasia": 9,
    "not_specified|EXOC2-related_disorder": 1,
    "FOXF2-related_disorder": 16,
    "not_specified|FOXF2-related_disorder": 1,
    "FOXC1-related_disorder": 17,
    "Axenfeld-Rieger_syndrome_type_3": 334,
    "Anterior_segment_dysgenesis_3|not_provided": 1,
    "FOXC1-related_disorder|Axenfeld-Rieger_syndrome_type_3": 3,
    "Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3": 79,
    "Axenfeld-Rieger_syndrome_type_3|not_provided": 20,
    "FOXC1-related_disorder|not_provided|Axenfeld-Rieger_syndrome_type_3": 2,
    "not_specified|Axenfeld-Rieger_syndrome_type_3|FOXC1-related_disorder|not_provided": 1,
    "Anterior_segment_dysgenesis_3": 13,
    "Axenfeld-Rieger_syndrome_type_3|FOXC1-related_disorder": 6,
    "Axenfeld-Rieger_syndrome_type_3|FOXC1-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3": 5,
    "Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3|not_provided": 3,
    "not_provided|Axenfeld-Rieger_syndrome_type_3": 22,
    "Axenfeld-Rieger_anomaly_with_partially_absent_eye_muscles|_distinctive_face|_hydrocephaly|_and_skeletal_abnormalities": 1,
    "Axenfeld-Rieger_syndrome_type_3|Inborn_genetic_diseases|Anterior_segment_dysgenesis_3": 2,
    "Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3": 7,
    "Inborn_genetic_diseases|Axenfeld-Rieger_syndrome_type_3": 10,
    "Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3|not_provided": 4,
    "FOXC1-related_disorder|Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3": 2,
    "Axenfeld-Rieger_syndrome_type_3|not_specified|not_provided": 2,
    "not_provided|Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3": 3,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3": 3,
    "Axenfeld-Rieger_syndrome_type_3|not_provided|FOXC1-related_disorder": 2,
    "FOXC1-related_disorder|not_specified|not_provided|Axenfeld-Rieger_syndrome_type_3": 1,
    "Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis": 2,
    "Inborn_genetic_diseases|Axenfeld-Rieger_syndrome_type_3|not_provided": 1,
    "Axenfeld-Rieger_syndrome_type_3|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3": 2,
    "Hypertelorism_and_tetralogy_of_fallot|Axenfeld-Rieger_syndrome_type_3": 1,
    "not_specified|not_provided|Axenfeld-Rieger_syndrome_type_3": 2,
    "Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3|Inborn_genetic_diseases": 3,
    "Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3|Inborn_genetic_diseases": 1,
    "Anterior_segment_dysgenesis_3|not_specified|not_provided|Axenfeld-Rieger_syndrome_type_3": 1,
    "Axenfeld-Rieger_syndrome_type_3|not_provided|Anterior_segment_dysgenesis_3": 1,
    "Axenfeld-Rieger_anomaly_with_partially_absent_eye_muscles|_distinctive_face|_hydrocephaly|_and_skeletal_abnormalities|Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3": 1,
    "Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3|not_provided|Inborn_genetic_diseases": 1,
    "Axenfeld-Rieger_syndrome_type_3|not_specified": 2,
    "Axenfeld-Rieger_syndrome_type_3|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Axenfeld-Rieger_syndrome_type_3|not_provided|not_specified": 1,
    "FOXC1-related_disorder|Axenfeld-Rieger_syndrome_type_3|Inborn_genetic_diseases": 1,
    "not_specified|Axenfeld-Rieger_syndrome_type_3|Anterior_segment_dysgenesis_3": 1,
    "not_specified|Axenfeld-Rieger_syndrome_type_3|FOXC1-related_disorder": 1,
    "not_provided|Axenfeld-Rieger_syndrome_type_3|not_specified": 1,
    "FOXC1-related_disorder|not_provided|not_specified|Axenfeld-Rieger_syndrome_type_3": 2,
    "Axenfeld-Rieger_syndrome_type_3|FOXC1-related_disorder|Inborn_genetic_diseases": 1,
    "Axenfeld-Rieger_syndrome_type_3|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Axenfeld-Rieger_syndrome_type_3": 1,
    "Alopecia|_androgenetic|_1": 2,
    "Axenfeld-Rieger_syndrome_type_3|FOXC1-related_disorder|not_provided": 1,
    "Anterior_segment_dysgenesis_3|Axenfeld-Rieger_syndrome_type_3|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|FOXC1-related_disorder|not_provided": 1,
    "WRNIP1-related_disorder": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_91": 2,
    "not_specified|SERPINB6-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_91": 4,
    "not_provided|SERPINB6-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_91": 4,
    "not_provided|not_specified|SERPINB6-related_disorder": 1,
    "SERPINB6-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_91|not_specified|not_provided": 1,
    "Usher_syndrome|not_provided|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_91": 1,
    "SERPINB6-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_91|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_91|not_specified": 1,
    "not_provided|SERPINB6-related_disorder": 1,
    "SERPINB6-related_disorder": 1,
    "Autoinflammation_with_episodic_fever_and_lymphadenopathy|Immunodeficiency_57|not_provided": 2,
    "RIPK1-related_disorder": 2,
    "not_provided|Immunodeficiency_57|Autoinflammation_with_episodic_fever_and_lymphadenopathy|not_specified": 1,
    "Autoinflammation_with_episodic_fever_and_lymphadenopathy": 4,
    "RIPK1-related_disorder|not_provided": 7,
    "Immunodeficiency_57": 4,
    "Immunodeficiency_57|not_provided": 5,
    "not_provided|RIPK1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency_57|Autoinflammation_with_episodic_fever_and_lymphadenopathy": 1,
    "Immunodeficiency_57|Autoinflammation_with_episodic_fever_and_lymphadenopathy": 1,
    "not_provided|Immunodeficiency_57|Inborn_genetic_diseases": 1,
    "IL10-related_early-onset_inflammatory_bowel_disease|Inborn_error_of_immunity|Immunodeficiency_57": 1,
    "Autoinflammation_with_episodic_fever_and_lymphadenopathy|not_provided": 2,
    "IL10-related_early-onset_inflammatory_bowel_disease|Inborn_error_of_immunity": 3,
    "not_provided|Immunodeficiency_57|Autoinflammation_with_episodic_fever_and_lymphadenopathy": 1,
    "not_provided|Inborn_genetic_diseases|Immunodeficiency_57": 1,
    "not_provided|See_cases|Autoinflammation_with_episodic_fever_and_lymphadenopathy|IL10-related_early-onset_inflammatory_bowel_disease|Inborn_error_of_immunity|Immunodeficiency_57": 1,
    "Autoinflammation_with_episodic_fever_and_lymphadenopathy|Immunodeficiency_57|not_specified|RIPK1-related_disorder|not_provided": 1,
    "not_provided|Immunodeficiency_57": 1,
    "Inborn_genetic_diseases|not_provided|RIPK1-related_disorder": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5": 11,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|See_cases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Complex_cortical_dysplasia_with_other_brain_malformations_5": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|not_provided|not_specified": 1,
    "Abnormal_cerebral_morphology|not_provided": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|TUBB2A-related_tubulinopathy": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|not_provided": 7,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|not_provided|TUBB2A-related_disorder|Seizure": 1,
    "Inborn_genetic_diseases|not_specified|Complex_cortical_dysplasia_with_other_brain_malformations_5|not_provided": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|Congenital_cerebellar_hypoplasia": 1,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_5": 4,
    "not_specified|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_5": 2,
    "TUBB2A-related_disorder": 5,
    "TUBB2A-related_tubulinopathy|Complex_cortical_dysplasia_with_other_brain_malformations_5|not_provided": 1,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_5|not_specified": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_5|TUBB2A-related_disorder": 1,
    "Tubulinopathy|Complex_cortical_dysplasia_with_other_brain_malformations_5|not_provided": 1,
    "not_provided|TUBB2A-related_disorder": 3,
    "TUBB2A-related_disorder|Complex_cortical_dysplasia_with_other_brain_malformations_5|not_specified|not_provided": 1,
    "TUBB2B-related_disorder": 7,
    "Complex_cortical_dysplasia_with_other_brain_malformations_7|not_specified": 1,
    "Lissencephaly|Complex_cortical_dysplasia_with_other_brain_malformations_7": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_7": 43,
    "not_provided|Tubulinopathy": 7,
    "Complex_cortical_dysplasia_with_other_brain_malformations_7|not_provided": 8,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_7": 10,
    "Complex_cortical_dysplasia_with_other_brain_malformations_1": 21,
    "Complex_cortical_dysplasia_with_other_brain_malformations_7|Lissencephaly": 1,
    "Congenital_bilateral_perisylvian_syndrome|Complex_cortical_dysplasia_with_other_brain_malformations_7": 1,
    "not_provided|not_specified|Complex_cortical_dysplasia_with_other_brain_malformations_7": 1,
    "Inborn_genetic_diseases|not_specified|TUBB2B-related_disorder|not_provided": 1,
    "not_provided|TUBB2B-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Complex_cortical_dysplasia_with_other_brain_malformations_7": 1,
    "Tubulinopathy": 33,
    "TUBB2B-related_tubulinopathy": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_7|Complex_cortical_dysplasia_with_other_brain_malformations_1": 1,
    "LYRM4-related_disorder": 4,
    "Combined_oxidative_phosphorylation_deficiency_19": 3,
    "LYRM4-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_deficiency_19": 1,
    "not_provided|Hereditary_spastic_paraplegia_77|Combined_oxidative_phosphorylation_defect_type_14": 1,
    "Combined_oxidative_phosphorylation_defect_type_14": 332,
    "Combined_oxidative_phosphorylation_defect_type_14|not_provided": 13,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_14": 11,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_14": 17,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_14": 4,
    "Combined_oxidative_phosphorylation_defect_type_14|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_14": 2,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_14": 2,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_14": 4,
    "Combined_oxidative_phosphorylation_defect_type_14|Inborn_genetic_diseases": 10,
    "FARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_14": 7,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_14": 3,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_14|Hereditary_spastic_paraplegia_77|FARS2-related_disorder": 1,
    "Hereditary_spastic_paraplegia_77": 4,
    "Global_developmental_delay|Mitochondrial_encephalomyopathy|not_provided|Combined_oxidative_phosphorylation_defect_type_14": 1,
    "Hereditary_spastic_paraplegia_77|not_provided|Combined_oxidative_phosphorylation_defect_type_14": 2,
    "FARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_14|not_specified|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_77|Combined_oxidative_phosphorylation_defect_type_14": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_14|Hereditary_spastic_paraplegia_77": 2,
    "FARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_14|not_provided": 1,
    "FARS2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|Hereditary_spastic_paraplegia_77": 2,
    "Combined_oxidative_phosphorylation_defect_type_14|not_specified": 3,
    "Inborn_genetic_diseases|See_cases|Combined_oxidative_phosphorylation_defect_type_14|not_provided|Hereditary_spastic_paraplegia_77": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_14|FARS2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|Hereditary_spastic_paraplegia_77|Inborn_genetic_diseases": 1,
    "Leigh_syndrome|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_14|Hereditary_spastic_paraplegia_77|not_provided|FARS2-related_disorder": 1,
    "not_specified|Hereditary_spastic_paraplegia_77|not_provided|Combined_oxidative_phosphorylation_defect_type_14": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_14|FARS2-related_disorder": 1,
    "not_provided|Autosomal_dominant_Alport_syndrome|FARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_14": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|Hereditary_spastic_paraplegia_77|not_provided": 1,
    "FARS2-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_77|Combined_oxidative_phosphorylation_defect_type_14|not_provided": 1,
    "FARS2-related_disorder|Hereditary_spastic_paraplegia_77|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_14|not_provided|See_cases": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|FARS2-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_14|not_provided|See_cases|Hereditary_spastic_paraplegia_77": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_14|Inborn_genetic_diseases|not_provided": 1,
    "Factor_XIII|_A_subunit|_deficiency_of": 84,
    "Factor_XIII|_A_subunit|_deficiency_of|not_provided": 7,
    "not_provided|Factor_XIII|_A_subunit|_deficiency_of": 11,
    "F13A1-related_disorder": 17,
    "Factor_XIII|_A_subunit|_deficiency_of|Thrombophilia_due_to_thrombin_defect": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|Inborn_genetic_diseases": 1,
    "F13A1-related_disorder|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "not_specified|not_provided|Factor_XIII|_A_subunit|_deficiency_of": 2,
    "not_provided|not_specified|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|Thrombophilia_due_to_thrombin_defect|Myocardial_infarction|_susceptibility_to|F13A1-related_disorder": 1,
    "Thrombophilia_due_to_thrombin_defect|not_specified": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|not_provided|F13A1-related_disorder": 2,
    "not_specified|Factor_XIII|_A_subunit|_deficiency_of": 3,
    "F13A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Factor_XIII|_A_subunit|_deficiency_of|not_provided": 2,
    "not_specified|F13A1-related_disorder": 1,
    "not_specified|Hereditary_factor_XIII_deficiency_disease|Factor_XIII|_A_subunit|_deficiency_of|not_provided": 1,
    "F13A1-related_disorder|not_provided|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "not_provided|F13A1-related_disorder": 1,
    "not_provided|not_specified|F13A1-related_disorder": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "not_provided|Intracranial_hemorrhage": 1,
    "not_specified|Factor_XIII|_A_subunit|_deficiency_of|Thrombophilia_due_to_thrombin_defect": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "Myocardial_infarction|_susceptibility_to|Factor_XIII|_A_subunit|_deficiency_of|Thrombophilia_due_to_thrombin_defect": 1,
    "Hereditary_factor_XIII_deficiency_disease": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|Thrombophilia_due_to_thrombin_defect|Myocardial_infarction|_susceptibility_to": 2,
    "Thrombophilia_due_to_thrombin_defect|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "Factor_XIII|_A_subunit|_deficiency_of|F13A1-related_disorder": 1,
    "F13A1-related_disorder|Inborn_genetic_diseases|not_provided|Factor_XIII|_A_subunit|_deficiency_of": 1,
    "Thrombophilia_due_to_thrombin_defect|Factor_XIII|_A_subunit|_deficiency_of|F13A1-related_disorder|not_provided": 1,
    "Venous_thrombosis|_protection_against|Factor_XIII|_A_subunit|_deficiency_of|Myocardial_infarction|_protection_against|not_specified|not_provided": 1,
    "RREB1-related_disorder|not_provided": 14,
    "RREB1-related_disorder": 17,
    "not_provided|RREB1-related_disorder": 21,
    "RREB1-associated_Noonan-like_syndrome": 1,
    "not_specified|RREB1-related_disorder": 1,
    "Neonatal_hemochromatosis": 3,
    "Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 3,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8": 14,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Woolly_hair-skin_fragility_syndrome": 4,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 596,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 27,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1020,
    "not_provided|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 33,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 16,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 22,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 406,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 59,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2": 1,
    "DSP-related_disorder": 11,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 109,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 13,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 85,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 109,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 18,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 22,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 5,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 52,
    "Arrhythmogenic_right_ventricular_dysplasia_8": 32,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|DSP-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 30,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Right_ventricular_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 7,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified": 9,
    "not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 27,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 5,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1S|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy": 3,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 36,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiovascular_phenotype|not_provided|DSP-related_disorder|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 11,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy": 6,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 118,
    "Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 8,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 11,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 12,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 5,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 13,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 37,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 17,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 5,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 64,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 43,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "DSP-related_disorder|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|not_specified|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 5,
    "Primary_dilated_cardiomyopathy|Long_QT_syndrome|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 22,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 8,
    "Lethal_acantholytic_epidermolysis_bullosa": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 25,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy|not_provided": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 12,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype": 14,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 11,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 16,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|not_specified": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|Collapse_(finding)": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Ventricular_tachycardia|not_specified|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|not_provided|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype": 7,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 4,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|not_provided": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiovascular_phenotype": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 3,
    "Keratosis_palmoplantaris_striata_2": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 5,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 6,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "not_provided|DSP-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 2,
    "Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Combined_pulmonary_fibrosis-emphysema_syndrome|not_provided|Chronic_obstructive_pulmonary_disease|Interstitial_lung_disease_2": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "DSP-related_disorder|Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 9,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified": 3,
    "not_provided|Cardiomyopathy|DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 4,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 6,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|not_provided|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 7,
    "not_specified|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Sudden_unexplained_death": 5,
    "Cardiovascular_phenotype|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy": 3,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 4,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 2,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 26,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 9,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|DSP-related_disorder": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_arrhythmogenic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided": 1,
    "Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|DSP-related_disorder|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "Arrhythmogenic_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 3,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "DSP-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 10,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 2,
    "not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Ventricular_tachycardia|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy": 6,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided": 8,
    "Woolly_hair-skin_fragility_syndrome|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Palmoplantar_blistering|Skin_fragility_with_non-scarring_blistering": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 2,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 13,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|DSP-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified": 3,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Global_developmental_delay|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|DSP-related_disorder": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified": 4,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 3,
    "Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Ventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|not_provided": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 5,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiac_arrest|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 3,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_specified|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "Left_ventricular_noncompaction_cardiomyopathy|Ventricular_tachycardia|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_dilated_cardiomyopathy": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder|Cardiomyopathy": 1,
    "Myocarditis": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 2,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrest": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Cardiomyopathy|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_2|not_provided": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy": 1,
    "Bicuspid_aortic_valve|Aortic_dilatation|Cardiac_arrhythmia|Sudden_cardiac_death|Ventricular_fibrillation|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 3,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Subvalvular_aortic_stenosis": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|not_specified|not_provided": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|DSP-related_disorder": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_specified|not_provided": 1,
    "Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|DSP-related_disorder": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_specified|Cardiovascular_phenotype|Left_ventricular_hypertrophy|Sudden_death|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy": 1,
    "Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|DSP-related_disorder|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Familial_restrictive_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiac_arrest|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_dilated_cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 2,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Left_ventricular_noncompaction": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 11,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy": 1,
    "not_provided|DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_specified|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|not_specified": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|DSP-related_disorder|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Ventricular_fibrillation|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 3,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|DSP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|DSP-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_1": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 3,
    "Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 4,
    "Cardiomyopathy|DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified": 1,
    "not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 4,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1S|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_provided|not_specified|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided": 1,
    "Cardiomyopathy|DSP-related_disorder|not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Wolff-Parkinson-White_pattern|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_familial_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Right_ventricular_cardiomyopathy|Ventricular_arrhythmia": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Long_QT_syndrome|Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Long_QT_syndrome|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Non-compaction_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|not_specified|Cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|not_provided": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 2,
    "not_specified|DSP-related_disorder|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "DSP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 3,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|DSP-related_disorder|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "Cardiovascular_phenotype|Sudden_unexplained_death|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "not_specified|not_provided|DSP-related_disorder|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Myocarditis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 3,
    "not_specified|Cardiomyopathy|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Restrictive_cardiomyopathy|Long_QT_syndrome|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|DSP-related_disorder|Cardiovascular_phenotype|Restrictive_cardiomyopathy|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Ventricular_tachycardia|DSP-related_disorder|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified": 1,
    "Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "DSP-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided": 2,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "not_provided|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 4,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|not_provided": 1,
    "DSP-related_disorder|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|DSP-related_disorder|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Progressive_familial_heart_block": 2,
    "Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_dysplasia_1|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|DSP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_specified|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|DSP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Migraine|Primary_dilated_cardiomyopathy|Hemiplegia": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Long_QT_syndrome|Hypertrophic_cardiomyopathy|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Hypertrophic_cardiomyopathy_2|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|Primary_dilated_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_provided|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|DSP-related_disorder|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|not_specified": 1,
    "Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_specified|DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified": 1,
    "DSP-related_disorder|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Keratosis_palmoplantaris_striata_2|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Primary_dilated_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|DSP-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Palmoplantar_blistering|Skin_fragility_with_non-scarring_blistering": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified": 2,
    "not_provided|not_specified|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder": 1,
    "DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Woolly_hair-skin_fragility_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|DSP-related_disorder|not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|DSP-related_disorder|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiomyopathy|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_dilated_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype": 7,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "DSP-related_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified|Cardiomyopathy|Amyloidosis|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2": 1,
    "not_specified|DSP-related_disorder": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_provided|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided": 2,
    "DSP-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "DSP-related_disorder|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|DSP-related_disorder|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|not_provided|not_specified": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_specified": 1,
    "not_provided|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiomyopathy|DSP-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Skin_fragility-woolly_hair-palmoplantar_keratoderma_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Woolly_hair-skin_fragility_syndrome|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Paroxysmal_familial_ventricular_fibrillation|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Cardiac_arrest|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "not_provided|Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "not_specified|DSP-related_disorder|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Cardiomyopathy|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|not_provided|DSP-related_disorder": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|not_specified": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Hypertrophic_cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|not_provided|Cardiomyopathy|Long_QT_syndrome": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "not_specified|Cardiomyopathy|DSP-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|not_provided|Cardiomyopathy": 1,
    "DSP-related_disorder|Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|not_provided": 1,
    "not_provided|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "DSP-related_disorder|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_specified|Lethal_acantholytic_epidermolysis_bullosa|not_provided|Cardiovascular_phenotype": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|DSP-related_disorder|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_provided|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_dilated_cardiomyopathy|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Palmoplantar_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Systolic_heart_failure|Hypertrophic_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|DSP-related_disorder|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|not_provided": 1,
    "not_provided|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|not_specified|DSP-related_disorder|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Primary_dilated_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|DSP-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Woolly_hair-skin_fragility_syndrome": 1,
    "Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Woolly_hair-skin_fragility_syndrome|Keratosis_palmoplantaris_striata_2|Arrhythmogenic_right_ventricular_dysplasia_8|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Brugada_syndrome_1|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Lethal_acantholytic_epidermolysis_bullosa": 1,
    "not_specified|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|not_provided": 1,
    "Woolly_hair-skin_fragility_syndrome|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Keratosis_palmoplantaris_striata_2|Lethal_acantholytic_epidermolysis_bullosa|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Keratosis_palmoplantaris_striata_2|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis": 1,
    "Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_8": 1,
    "Long_QT_syndrome|Ventricular_tachycardia|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Cardiomyopathy|_dilated|_with_wooly_hair|_keratoderma|_and_tooth_agenesis|Keratosis_palmoplantaris_striata_2": 1,
    "not_specified|not_provided|Arrhythmogenic_cardiomyopathy_with_wooly_hair_and_keratoderma|Arrhythmogenic_right_ventricular_dysplasia_8|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "not_provided|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "Woolly_hair-skin_fragility_syndrome|Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_dysplasia_8": 2,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Lethal_acantholytic_epidermolysis_bullosa|Woolly_hair-skin_fragility_syndrome": 1,
    "Lethal_acantholytic_epidermolysis_bullosa|Arrhythmogenic_right_ventricular_cardiomyopathy|Epidermolysis_bullosa_simplex_due_to_plakophilin_deficiency|Woolly_hair-skin_fragility_syndrome": 3,
    "not_provided|Neonatal_hemochromatosis": 1,
    "BMP6-related_disorder": 20,
    "Iron_overload|_susceptibility_to": 4,
    "Iron_overload|_susceptibility_to|not_provided": 2,
    "BMP6-related_disorder|Iron_overload|_susceptibility_to|not_provided": 2,
    "not_provided|BMP6-related_disorder": 1,
    "TXNDC5-related_condition": 1,
    "Hermansky-Pudlak_syndrome_11|Hermansky-Pudlak_syndrome": 1,
    "BLOC1S5-related_disorder": 2,
    "Hermansky-Pudlak_syndrome_11": 3,
    "Branchiooculofacial_syndrome": 42,
    "TFAP2A-related_disorder": 9,
    "Branchiooculofacial_syndrome|not_provided": 13,
    "Inborn_genetic_diseases|Branchiooculofacial_syndrome|not_provided": 2,
    "Microphthalmia|Epicanthus|Hypertelorism|Esotropia|Lens_subluxation|Amblyopia|Abnormality_of_visual_evoked_potentials|Short_neck|High_palate|Low-set_ears|EEG_abnormality|Iris_coloboma|Nystagmus|Branchiooculofacial_syndrome": 1,
    "not_provided|Branchiooculofacial_syndrome": 14,
    "not_provided|Chromatinopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Branchiooculofacial_syndrome": 1,
    "Branchiooculofacial_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|TFAP2A-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Branchiooculofacial_syndrome": 1,
    "TFAP2A-related_disorder|Branchiooculofacial_syndrome": 1,
    "TFAP2A-related_disorder|not_provided": 2,
    "TFAP2A-related_disorder|Inborn_genetic_diseases": 1,
    "Branchiooculofacial_syndrome|TFAP2A-related_disorder|not_provided": 2,
    "Branchiooculofacial_syndrome|TFAP2A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Branchiooculofacial_syndrome": 1,
    "Melnick-Fraser_syndrome": 168,
    "Cataract_13_with_adult_I_phenotype|GCNT2-related_disorder": 1,
    "GCNT2-related_disorder": 10,
    "GCNT2-related_disorder|not_provided": 1,
    "ADULT_i_BLOOD_GROUP_PHENOTYPE": 2,
    "Cataract_13_with_adult_I_phenotype|Inborn_genetic_diseases": 2,
    "not_provided|GCNT2-related_disorder": 1,
    "Blood_group|_I_system|not_provided": 1,
    "Adult_i_blood_group_with_or_without_congenital_cataract": 7,
    "Blood_group|_I_system": 73,
    "Blood_group|_I_system|not_provided|Cataract_13_with_adult_I_phenotype": 1,
    "not_provided|Cataract_13_with_adult_I_phenotype|not_specified|Blood_group|_I_system": 1,
    "GCNT2-related_disorder|Blood_group|_I_system|Cataract_13_with_adult_I_phenotype": 2,
    "Cataract_13_with_adult_I_phenotype|Blood_group|_I_system": 1,
    "not_provided|Blood_group|_I_system|Cataract_13_with_adult_I_phenotype": 2,
    "Blood_group|_I_system|Cataract_13_with_adult_I_phenotype": 1,
    "Cataract_13_with_adult_I_phenotype|not_specified": 1,
    "not_provided|Blood_group|_I_system": 4,
    "not_provided|Cataract_13_with_adult_I_phenotype": 2,
    "not_provided|not_specified|Cataract_13_with_adult_I_phenotype": 1,
    "not_specified|Blood_group|_I_system": 1,
    "Cataract_13_with_adult_I_phenotype|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_62": 8,
    "not_specified|not_provided|Retinitis_pigmentosa_62|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinitis_pigmentosa_62": 6,
    "MAK-related_disorder|not_provided": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_62": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Retinitis_pigmentosa_62": 1,
    "Isolated_macular_dystrophy|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|MAK-related_disorder|Retinitis_pigmentosa_62": 1,
    "Retinitis_pigmentosa_62|not_provided": 4,
    "not_provided|MAK-related_retinopathy": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Retinitis_pigmentosa_62|Retinal_dystrophy|not_provided": 2,
    "Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive": 1,
    "not_specified|not_provided|Retinitis_Pigmentosa|_Recessive": 1,
    "MAK-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_62|Retinitis_pigmentosa": 2,
    "Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_62|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa_62": 1,
    "not_provided|Retinitis_pigmentosa_62|Inborn_genetic_diseases": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_62": 1,
    "not_provided|MAK-related_disorder": 1,
    "Retinitis_pigmentosa_62|Retinal_dystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_62": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_62|Retinal_dystrophy|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|MAK-related_disorder|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_62": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_62": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_62|not_provided": 1,
    "MAK-related_disorder|not_provided|Retinitis_pigmentosa_62": 1,
    "Familial_hypoparathyroidism|not_provided": 8,
    "GCM2-related_disorder": 3,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4": 40,
    "Familial_hypoparathyroidism|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2": 1,
    "Inborn_genetic_diseases|Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4": 2,
    "Hypoparathyroidism|_familial_isolated|_2": 9,
    "Hyperparathyroidism_4": 4,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hypoparathyroidism": 8,
    "Familial_hypoparathyroidism|Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|Inborn_genetic_diseases": 1,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|not_provided": 3,
    "Familial_hypoparathyroidism|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|not_provided": 1,
    "Inborn_genetic_diseases|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2": 3,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|not_specified": 1,
    "not_provided|GCM2-related_disorder": 4,
    "GCM2-related_disorder|not_specified|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|not_provided": 1,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|not_specified|Familial_hypoparathyroidism|not_provided": 1,
    "GCM2-related_disorder|Inborn_genetic_diseases": 1,
    "GCM2-related_disorder|not_provided": 4,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2": 2,
    "Familial_hypoparathyroidism|not_provided|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2": 2,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|not_provided": 2,
    "Familial_hypoparathyroidism|not_provided|Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4": 1,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|not_provided|Familial_hypoparathyroidism": 1,
    "not_specified|Familial_hypoparathyroidism|not_provided": 1,
    "GCM2-related_disorder|not_provided|Familial_hypoparathyroidism": 1,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4": 1,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|GCM2-related_disorder|Inborn_genetic_diseases": 1,
    "GCM2-related_disorder|Familial_hypoparathyroidism": 1,
    "GCM2-related_disorder|Familial_hypoparathyroidism|not_provided": 2,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|Familial_hypoparathyroidism|not_provided": 1,
    "Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4|not_provided|GCM2-related_disorder": 1,
    "not_provided|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2": 2,
    "not_provided|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|GCM2-related_disorder": 1,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|Inborn_genetic_diseases|Familial_hypoparathyroidism": 1,
    "GCM2-related_disorder|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|not_provided": 1,
    "not_provided|not_specified|Familial_hypoparathyroidism|Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|GCM2-related_disorder": 1,
    "not_provided|not_specified|Familial_hypoparathyroidism|GCM2-related_disorder": 1,
    "not_provided|Hypoparathyroidism|_familial_isolated|_2": 1,
    "not_provided|Hypoparathyroidism|_familial_isolated|_2|Hyperparathyroidism_4": 1,
    "Hyperparathyroidism_4|Hypoparathyroidism|_familial_isolated|_2|Familial_hypoparathyroidism": 1,
    "Premature_ovarian_failure_24": 2,
    "NEDD9-related_disorder|not_provided": 1,
    "HIVEP1-related_disorder|not_specified": 3,
    "HIVEP1-related_disorder": 8,
    "not_provided|HIVEP1-related_disorder": 1,
    "Attention_deficit_hyperactivity_disorder|Hearing_impairment|Seizure|Compulsive_behaviors|not_specified": 2,
    "HIVEP1-related_disorder|not_provided|not_specified": 1,
    "not_specified|HIVEP1-related_disorder": 2,
    "Question_mark_ears|_isolated|Auriculocondylar_syndrome_3|Inborn_genetic_diseases": 1,
    "EDN1-related_disorder": 4,
    "EDN1-related_disorder|not_provided": 1,
    "not_provided|Question_mark_ears|_isolated": 1,
    "Question_mark_ears|_isolated": 2,
    "Auriculocondylar_syndrome_3": 2,
    "not_provided|Auriculocondylar_syndrome_3": 1,
    "Question_mark_ears|_isolated|Auriculocondylar_syndrome_3": 1,
    "not_provided|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_7|Auriculocondylar_syndrome_3": 1,
    "Developmental_and_epileptic_encephalopathy|_70": 28,
    "not_provided|PHACTR1-related_disorder": 3,
    "PHACTR1-related_disorder": 18,
    "PHACTR1-related_disorder|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_70|not_specified": 3,
    "not_specified|Developmental_and_epileptic_encephalopathy|_70": 2,
    "TBC1D7-related_disorder|not_provided": 4,
    "Macrocephaly|not_provided": 1,
    "Macrocephaly/megalencephaly_syndrome|_autosomal_recessive|not_provided": 1,
    "Macrocephaly/megalencephaly_syndrome|_autosomal_recessive": 3,
    "TBC1D7-related_disorder|not_specified": 1,
    "not_specified|TBC1D7-related_disorder|not_provided": 1,
    "TBC1D7-related_disorder": 6,
    "not_provided|Macrocephaly/megalencephaly_syndrome|_autosomal_recessive": 2,
    "not_provided|TBC1D7-related_disorder": 1,
    "SIRT5-related_disorder": 1,
    "Wolff-Parkinson-White_pattern|Highly_elevated_creatine_kinase|Pes_cavus|Skeletal_myopathy|Muscular_atrophy": 1,
    "JARID2-related_disorder": 23,
    "Speech_apraxia|Stereotypic_movement_disorder|Autism|Intellectual_disability": 1,
    "JARID2-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_delay_with_variable_intellectual_disability_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_delay_with_variable_intellectual_disability_and_dysmorphic_facies": 1,
    "Developmental_delay_with_variable_intellectual_disability_and_dysmorphic_facies": 14,
    "JARID2-related_disorder|not_provided": 5,
    "JARID2-related_Neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|JARID2-related_disorder": 1,
    "Intellectual_disability|_mild": 3,
    "Inborn_genetic_diseases|Developmental_delay_with_variable_intellectual_disability_and_dysmorphic_facies": 1,
    "JARID2-associated_Neurodevelopmental_disorder": 2,
    "Developmental_delay_with_variable_intellectual_disability_and_dysmorphic_facies|Neurodevelopmental_disorder": 1,
    "Developmental_delay_with_variable_intellectual_disability_and_dysmorphic_facies|not_provided": 2,
    "JARID2-related_Neurodevelopmental_Disorder": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome": 2,
    "DTNBP1-related_disorder": 3,
    "DTNBP1-related_disorder|not_provided": 3,
    "Hermansky-Pudlak_syndrome_7": 5,
    "DTNBP1-related_disorder|not_specified|not_provided|Hermansky-Pudlak_syndrome_7": 1,
    "not_provided|Hermansky-Pudlak_syndrome_7": 4,
    "not_provided|DTNBP1-related_disorder": 3,
    "DTNBP1-related_disorder|not_provided|not_specified": 1,
    "not_provided|DTNBP1-related_disorder|not_specified": 1,
    "DTNBP1-related_disorder|Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_7": 1,
    "Hermansky-Pudlak_syndrome|not_provided|not_specified": 2,
    "Hermansky-Pudlak_syndrome_7|not_provided": 2,
    "MYLIP-related_disorder": 1,
    "not_provided|GMPR_POLYMORPHISM": 1,
    "ATXN1-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Spinocerebellar_ataxia_type_1|not_specified": 2,
    "ATXN1-related_disorder": 18,
    "Spinocerebellar_ataxia_type_1|Tip-toe_gait|not_provided": 1,
    "ATXN1-related_disorder|Spinocerebellar_ataxia_type_1|not_specified": 1,
    "ATXN1-related_disorder|not_provided": 2,
    "Spinocerebellar_ataxia_type_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "ATXN1-related_disorder|not_specified|Spinocerebellar_ataxia_type_1": 1,
    "not_specified|ATXN1-related_disorder": 1,
    "not_provided|not_specified|ATXN1-related_disorder": 1,
    "ATXN1-related_disorder|not_provided|not_specified": 1,
    "not_specified|Spinocerebellar_ataxia_type_1": 1,
    "Inborn_genetic_diseases|ATXN1-related_disorder|Spinocerebellar_ataxia_type_1": 1,
    "Cardiomyopathy|_dilated|_2I": 5,
    "not_specified|Cardiomyopathy|_dilated|_2I": 1,
    "CAP2-associated_dilated_cardiomyopathy": 1,
    "not_specified|Pulmonary_artery_atresia": 2,
    "Chiari_malformation|Intellectual_disability|_moderate|Apraxia|Speech_apraxia|Seizure": 1,
    "Lafora_disease": 239,
    "not_provided|Lafora_disease": 24,
    "Lafora_disease|not_provided": 11,
    "Lafora_disease|not_specified": 3,
    "Lafora_disease|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Lafora_disease": 15,
    "NHLRC1-related_disorder|not_specified|Lafora_disease": 1,
    "Inborn_genetic_diseases|Lafora_disease|not_provided": 6,
    "not_provided|Lafora_disease|Inborn_genetic_diseases": 3,
    "Lafora_disease|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Lafora_disease": 1,
    "Myoclonic_epilepsy_of_Lafora_2": 6,
    "Inborn_genetic_diseases|NHLRC1-related_disorder|Lafora_disease|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Lafora_disease": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Lafora_disease": 3,
    "Lafora_disease|Inborn_genetic_diseases|Myoclonic_epilepsy_of_Lafora_2": 1,
    "Lafora_disease|Myoclonic_epilepsy_of_Lafora_1": 2,
    "Lafora_disease|Inborn_genetic_diseases|NHLRC1-related_disorder|not_provided": 1,
    "Myoclonic_epilepsy_of_Lafora_1": 10,
    "not_provided|Lafora_disease|Myoclonic_epilepsy_of_Lafora_2": 2,
    "Inborn_genetic_diseases|not_specified|Lafora_disease": 1,
    "Lafora_disease|Inborn_genetic_diseases|not_provided|Myoclonic_epilepsy_of_Lafora_1|NHLRC1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Lafora_disease|Myoclonic_epilepsy_of_Lafora_2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Lafora_disease|Myoclonic_epilepsy_of_Lafora_2": 1,
    "NHLRC1-related_disorder|not_provided|Lafora_disease|Inborn_genetic_diseases": 1,
    "Lafora_disease|Myoclonic_epilepsy_of_Lafora_2|not_provided": 1,
    "Lafora_disease|Myoclonic_epilepsy_of_Lafora_2": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Lafora_disease": 1,
    "not_specified|Lafora_disease": 2,
    "Myoclonic_epilepsy_of_Lafora_1|NHLRC1-related_disorder|not_provided|Lafora_disease|Myoclonic_epilepsy_of_Lafora_2": 1,
    "Myoclonic_epilepsy_of_Lafora_1|NHLRC1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Lafora_disease|Myoclonic_epilepsy_of_Lafora_2": 1,
    "Myoclonic_epilepsy_of_Lafora_1|NHLRC1-related_disorder|Inborn_genetic_diseases|not_provided|Lafora_disease": 1,
    "Thiopurine_S-methyltransferase_deficiency": 10,
    "not_provided|Thiopurine_S-methyltransferase_deficiency": 1,
    "Thiopurine_response": 4,
    "TPMT-related_disorder|not_provided|Thiopurine_S-methyltransferase_deficiency": 1,
    "TPMT-related_disorder|Azathioprine_response": 1,
    "TPMT-related_disorder": 1,
    "Normal_pregnancy|Preeclampsia": 2,
    "E2F3-related_disorder": 1,
    "Coffin-Siris_syndrome_10": 30,
    "SOX4-related_disorder": 9,
    "SOX4-related_disorder|not_provided": 7,
    "Coffin-Siris_syndrome_10|Intellectual_disability|Developmental_delay|Mild_facial_and_digital_morphological_abnormalities": 3,
    "Intellectual_disability|_mild|Mild_facial_and_digital_morphological_abnormalities|Developmental_delay|Intellectual_disability|Coffin-Siris_syndrome_10": 1,
    "Inborn_genetic_diseases|SOX4-related_disorder": 1,
    "SOX4-related_neurodevelopmental_disorder": 1,
    "not_provided|SOX4-related_disorder": 3,
    "not_provided|Coffin-Siris_syndrome_10": 2,
    "not_provided|Coffin-Siris_syndrome_10|SOX4-related_disorder": 1,
    "Coffin-Siris_syndrome_10|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_10|not_provided": 3,
    "DCDC2-related_disorder": 15,
    "not_provided|Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 2,
    "Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 38,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|DCDC2-related_disorder|not_provided": 4,
    "not_provided|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_specified|not_provided": 2,
    "Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|Inborn_genetic_diseases|not_provided": 1,
    "DCDC2-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 45,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|DCDC2-related_disorder": 6,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19": 3,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66": 24,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Nonsyndromic_Deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Inborn_genetic_diseases": 2,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "DCDC2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "DCDC2-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|DCDC2-related_disorder": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|Inborn_genetic_diseases": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 5,
    "Inborn_genetic_diseases|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided|Nephronophthisis_19|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19": 5,
    "Isolated_neonatal_sclerosing_cholangitis": 6,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_specified|Nephronophthisis_19|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|not_provided": 2,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided": 4,
    "not_provided|Nephronophthisis_19|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_specified|Nephronophthisis_19": 2,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|DCDC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|DCDC2-related_disorder|Inborn_genetic_diseases": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|DCDC2-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|Inborn_genetic_diseases|not_provided": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|not_provided": 1,
    "DCDC2-related_disorder|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|not_provided": 1,
    "DCDC2-related_disorder|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66": 1,
    "Nephronophthisis_19": 5,
    "DCDC2-related_disorder|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|not_provided|not_specified": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided|not_specified": 1,
    "DCDC2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_provided": 2,
    "not_provided|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|Inborn_genetic_diseases": 1,
    "Nephronophthisis_19|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided": 1,
    "not_provided|DCDC2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|Isolated_neonatal_sclerosing_cholangitis|DCDC2-related_disorder": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|DCDC2-related_disorder": 1,
    "not_provided|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|DCDC2-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19": 1,
    "DCDC2-related_disorder|Nephronophthisis_19": 1,
    "DCDC2-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided|Inborn_genetic_diseases": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|DCDC2-related_disorder|not_specified|not_provided": 1,
    "DCDC2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_specified": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Inborn_genetic_diseases|Nephronophthisis_19|not_provided": 1,
    "Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_provided": 3,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided|DCDC2-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_specified|Nephronophthisis_19": 1,
    "DCDC2-related_disorder|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided": 1,
    "Inborn_genetic_diseases|Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66": 1,
    "Isolated_neonatal_sclerosing_cholangitis|Autosomal_recessive_nonsyndromic_hearing_loss_66|Nephronophthisis_19|DCDC2-related_disorder|Inborn_genetic_diseases": 1,
    "DCDC2-related_disorder|not_provided": 1,
    "not_provided|not_specified|DCDC2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Inborn_genetic_diseases|Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|not_specified": 2,
    "Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|Autosomal_recessive_nonsyndromic_hearing_loss_66|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|Nephronophthisis_19|not_provided|Dyslexia|_susceptibility_to|_2": 1,
    "Neonatal_ichthyosis-sclerosing_cholangitis_syndrome|Isolated_neonatal_sclerosing_cholangitis": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_66|Isolated_neonatal_sclerosing_cholangitis|DCDC2-related_disorder": 1,
    "ALDH5A1-related_disorder": 3,
    "Succinate-semialdehyde_dehydrogenase_deficiency": 614,
    "ALDH5A1-related_disorder|not_specified|Succinate-semialdehyde_dehydrogenase_deficiency|not_provided": 2,
    "Seizure|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency|not_specified": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|not_provided": 39,
    "not_provided|Succinate-semialdehyde_dehydrogenase_deficiency": 48,
    "Inborn_genetic_diseases|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency": 5,
    "Succinate-semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases": 5,
    "Succinate-semialdehyde_dehydrogenase_deficiency|not_provided|ALDH5A1-related_disorder": 2,
    "Inborn_genetic_diseases|Succinate-semialdehyde_dehydrogenase_deficiency": 12,
    "not_provided|ALDH5A1-related_disorder|Succinate-semialdehyde_dehydrogenase_deficiency": 1,
    "ALDH5A1-related_disorder|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency": 2,
    "Succinate-semialdehyde_dehydrogenase_deficiency|not_provided|not_specified": 4,
    "not_specified|Succinate-semialdehyde_dehydrogenase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Succinate-semialdehyde_dehydrogenase_deficiency": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|Succinate-semialdehyde_dehydrogenase_deficiency": 2,
    "ALDH5A1-related_disorder|not_provided|not_specified|Succinate-semialdehyde_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|Succinate-semialdehyde_dehydrogenase_deficiency|not_provided|not_specified": 1,
    "not_provided|Succinate-semialdehyde_dehydrogenase_deficiency|not_specified": 2,
    "not_specified|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency": 2,
    "ALDH5A1-related_disorder|Inborn_genetic_diseases|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency": 1,
    "Intellectual_disability|Succinate-semialdehyde_dehydrogenase_deficiency|not_provided": 1,
    "ALDH5A1-related_disorder|not_specified|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|Intellectual_disability|not_provided": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|See_cases|Inborn_genetic_diseases": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|not_specified|ALDH5A1-related_disorder|not_provided": 1,
    "not_provided|Succinate-semialdehyde_dehydrogenase_deficiency|ALDH5A1-related_disorder": 1,
    "not_specified|not_provided|Succinate-semialdehyde_dehydrogenase_deficiency|Intellectual_disability": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|not_specified|ALDH5A1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Succinate-semialdehyde_dehydrogenase_deficiency|not_provided": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|not_provided|See_cases": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|EEG_abnormality|not_provided": 1,
    "Succinate-semialdehyde_dehydrogenase_deficiency|ALDH5A1-related_disorder": 1,
    "not_specified|Succinate-semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Succinate-semialdehyde_dehydrogenase_deficiency|not_provided": 1,
    "KIAA0319-related_disorder": 14,
    "not_provided|KIAA0319-related_disorder": 2,
    "not_specified|KIAA0319-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_23": 6,
    "TDP2-related_disorder": 2,
    "not_provided|TDP2-related_disorder": 3,
    "TDP2-related_disorder|not_provided": 2,
    "GMNN-related_disorder": 1,
    "Meier-Gorlin_syndrome_6|Meier-Gorlin_syndrome": 3,
    "GMNN-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Meier-Gorlin_syndrome_6": 1,
    "not_provided|GMNN-related_disorder": 1,
    "Meier-Gorlin_syndrome_6": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_104|not_specified": 3,
    "RIPOR2-related_disorder|not_specified|not_provided": 2,
    "not_provided|RIPOR2-related_disorder": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_104|not_specified|not_provided": 1,
    "RIPOR2-related_disorder|not_provided": 4,
    "not_provided|not_specified|RIPOR2-related_disorder": 2,
    "not_specified|RIPOR2-related_disorder|not_provided": 1,
    "RIPOR2-related_disorder": 8,
    "not_specified|not_provided|RIPOR2-related_disorder": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_21|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_104": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_21|Autosomal_recessive_nonsyndromic_hearing_loss_104|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_104|Autosomal_dominant_nonsyndromic_hearing_loss_21|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_21|Autosomal_recessive_nonsyndromic_hearing_loss_104|RIPOR2-related_disorder": 1,
    "not_specified|RIPOR2-related_disorder": 1,
    "SCGN-related_disorder|not_provided": 1,
    "SCGN-related_disorder": 1,
    "SLC17A3-related_disorder": 5,
    "Uric_acid_concentration|_serum|_quantitative_trait_locus_4": 2,
    "Doxorubicin_response": 1,
    "not_provided|Hereditary_hemochromatosis": 11,
    "Hemochromatosis_type_1": 29,
    "Hemochromatosis_type_1|Hereditary_hemochromatosis": 5,
    "HFE-related_disorder": 1,
    "HFE-related_disorder|Microvascular_complications_of_diabetes|_susceptibility_to|_7|Variegate_porphyria|Alzheimer_disease_type_1|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|not_provided|Hereditary_hemochromatosis|not_specified": 1,
    "Hereditary_hemochromatosis|HFE-related_disorder|Hemochromatosis_type_1|not_provided": 1,
    "not_provided|Hereditary_hemochromatosis|Hemochromatosis_type_1": 1,
    "HFE-related_disorder|Hereditary_hemochromatosis|Hemochromatosis_type_1|not_provided": 2,
    "Hereditary_hemochromatosis|not_provided|Hemochromatosis_type_1": 4,
    "Alzheimer_disease_type_1|Hereditary_hemochromatosis": 1,
    "not_provided|HFE_POLYMORPHISM|Hemochromatosis_type_1": 1,
    "Hemochromatosis_type_1|not_specified|HFE_POLYMORPHISM": 1,
    "Hemochromatosis_type_1|Bronze_diabetes|Neuroendocrine_neoplasm|Microvascular_complications_of_diabetes|_susceptibility_to|_7|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|Variegate_porphyria|Alzheimer_disease|Hereditary_hemochromatosis|not_specified|not_provided|Cardiomyopathy|Cystic_fibrosis|See_cases": 1,
    "Hemochromatosis_type_1|Inborn_genetic_diseases|not_provided|Hereditary_hemochromatosis": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_7|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|Hemochromatosis_type_1|Alzheimer_disease_type_1|Variegate_porphyria|HFE-related_disorder|Alzheimer_disease|Hereditary_hemochromatosis|not_specified|not_provided": 1,
    "not_specified|not_provided|Hemochromatosis_type_1": 1,
    "not_specified|Hereditary_hemochromatosis": 1,
    "Hemochromatosis_type_1|not_provided": 4,
    "not_specified|Hemochromatosis_type_1": 2,
    "Hereditary_hemochromatosis|Hemochromatosis_type_1": 3,
    "Hemochromatosis_type_1|Hereditary_hemochromatosis|not_provided|not_specified": 1,
    "Hereditary_hemochromatosis|Inborn_genetic_diseases": 6,
    "not_provided|Hemochromatosis_type_1|Hereditary_hemochromatosis": 1,
    "not_provided|Hereditary_hemochromatosis|not_specified": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_7|Variegate_porphyria|Alzheimer_disease_type_1|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|not_specified|Hereditary_hemochromatosis|not_provided": 1,
    "HFE-related_disorder|Hereditary_hemochromatosis": 1,
    "Variegate_porphyria|Alzheimer_disease_type_1|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|Microvascular_complications_of_diabetes|_susceptibility_to|_7|Hereditary_hemochromatosis": 1,
    "Hemochromatosis_type_1|Juvenile_hemochromatosis": 1,
    "Variegate_porphyria|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|Microvascular_complications_of_diabetes|_susceptibility_to|_7|Alzheimer_disease_type_1|Hereditary_hemochromatosis": 1,
    "Inborn_genetic_diseases|Hereditary_hemochromatosis": 8,
    "Hereditary_hemochromatosis|Familial_porphyria_cutanea_tarda|Variegate_porphyria|Alzheimer_disease_type_1|Hemochromatosis_type_1|Microvascular_complications_of_diabetes|_susceptibility_to|_7|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2": 1,
    "Hemochromatosis_type_1|HFE-related_disorder|Bronze_diabetes|Abnormality_of_the_nervous_system|Abnormality_of_the_male_genitalia|Peripheral_neuropathy|Abnormal_peripheral_nervous_system_morphology|Abdominal_pain|Atypical_behavior|Pain|Microvascular_complications_of_diabetes|_susceptibility_to|_7|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|Alzheimer_disease_type_1|Variegate_porphyria|Hereditary_hemochromatosis|Neuroendocrine_neoplasm|Juvenile_hemochromatosis|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Cardiomyopathy|Cutaneous_photosensitivity|Porphyrinuria": 1,
    "Hemochromatosis_type_1|Hereditary_hemochromatosis|not_provided|Incidental_Discovery": 1,
    "not_provided|HFE_INTRONIC_POLYMORPHISM": 1,
    "not_provided|HFE-related_disorder": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_7|Alzheimer_disease_type_1|Variegate_porphyria|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|not_provided|Hereditary_hemochromatosis": 1,
    "Hemochromatosis_type_1|not_provided|Hereditary_hemochromatosis": 1,
    "Alzheimer_disease_type_1|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Familial_porphyria_cutanea_tarda|Variegate_porphyria|Microvascular_complications_of_diabetes|_susceptibility_to|_7": 1,
    "not_provided|Hemochromatosis_type_1": 6,
    "Alzheimer_disease_type_1|Familial_porphyria_cutanea_tarda|Hemochromatosis_type_1|TRANSFERRIN_SERUM_LEVEL_QUANTITATIVE_TRAIT_LOCUS_2|Variegate_porphyria|Microvascular_complications_of_diabetes|_susceptibility_to|_7|not_provided": 1,
    "H4C3-related_disorder": 7,
    "not_provided|Tessadori-van_Haaften_neurodevelopmental_syndrome_1": 1,
    "not_provided|H4C3-related_disorder": 1,
    "Tessadori-van_Haaften_neurodevelopmental_syndrome_1": 4,
    "Tessadori-van_Haaften_neurodevelopmental_syndrome_1|not_specified": 1,
    "Tessadori-van_Haaften_neurodevelopmental_syndrome_1|HIST1H4C-associated_disorder": 1,
    "H1-4-related_disorder": 6,
    "not_provided|H1-4-related_disorder": 3,
    "H1-4-related_disorder|not_provided": 3,
    "not_specified|H1-4-related_disorder|not_provided": 1,
    "Rahman_syndrome": 20,
    "HIST1H1E-related_neurodevelopmental_disorder_with_multiple_anomalies|Rahman_syndrome|not_provided": 1,
    "not_specified|H1-4-related_disorder": 3,
    "Rahman_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Rahman_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Rahman_syndrome": 3,
    "not_provided|Rahman_syndrome|not_specified": 1,
    "Rahman_syndrome|not_provided": 2,
    "Pitt-Hopkins_syndrome|not_provided|Auditory_neuropathy_spectrum_disorder|Rahman_syndrome": 1,
    "Neurodevelopmental_disorder|Rahman_syndrome|not_provided": 1,
    "Rahman_syndrome|not_specified": 2,
    "not_specified|Syndromic_intellectual_disability": 1,
    "H4C5-related_disorder": 2,
    "Tessadori-Van_Haaften_neurodevelopmental_syndrome_3": 8,
    "not_provided|Tessadori-Van_Haaften_neurodevelopmental_syndrome_3|not_specified|See_cases": 1,
    "Tessadori-Van_Haaften_neurodevelopmental_syndrome_3|not_specified": 1,
    "BTN2A2-related_disorder": 15,
    "not_specified|BTN2A2-related_disorder": 3,
    "BTN2A2-related_disorder|not_provided": 1,
    "not_provided|BTN2A2-related_disorder": 1,
    "Craniosynostosis_7": 5,
    "Tessadori-Van_Haaften_neurodevelopmental_syndrome_4": 3,
    "Tessadori-van_Haaften_neurodevelopmental_syndrome_2": 6,
    "C3HEX|_ability_to_smell": 2,
    "Neurodevelopmental_disorder_with_language_delay_and_variable_cognitive_abnormalities": 6,
    "Neurodevelopmental_disorder_with_language_delay_and_variable_cognitive_abnormalities|Delayed_speech_and_language_development|Intellectual_disability|Global_developmental_delay": 3,
    "GABBR1-associated_neurodevelopmental_disorder": 1,
    "not_provided|GABBR1-related_neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_language_delay_and_variable_cognitive_abnormalities|Delayed_speech_and_language_development|Intellectual_disability|Motor_delay|Atypical_behavior|Global_developmental_delay": 1,
    "not_specified|Neurodevelopmental_disorder_with_language_delay_and_variable_cognitive_abnormalities": 1,
    "Narcolepsy_7": 2,
    "MOG-related_disorder|not_provided": 1,
    "MOG-related_disorder": 4,
    "Transient_Neonatal_Diabetes|_Recessive|not_provided": 1,
    "ZFP57-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Diabetes_mellitus|_transient_neonatal|_1|not_provided|ZFP57-related_disorder|Monogenic_diabetes": 1,
    "Diabetes_mellitus|_transient_neonatal|_1": 17,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_1": 5,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_1|not_provided": 1,
    "not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_1": 3,
    "not_provided|Monogenic_diabetes|Diabetes_mellitus|_transient_neonatal|_1|ZFP57-related_disorder": 1,
    "Diabetes_mellitus|_transient_neonatal|_1|Inborn_genetic_diseases": 2,
    "not_provided|Monogenic_diabetes|Diabetes_mellitus|_transient_neonatal|_1": 2,
    "Diabetes_mellitus|_transient_neonatal|_1|not_provided": 3,
    "Inborn_genetic_diseases|Diabetes_mellitus|_transient_neonatal|_1": 1,
    "ZFP57-related_disorder": 1,
    "ZFP57-related_disorder|not_provided|Monogenic_diabetes|not_specified|Diabetes_mellitus|_transient_neonatal|_1": 1,
    "ZFP57-related_disorder|not_provided|not_specified|Diabetes_mellitus|_transient_neonatal|_1": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_1|ZFP57-related_disorder|Monogenic_diabetes|Inborn_genetic_diseases": 1,
    "not_provided|Monogenic_diabetes|Diabetes_mellitus|_transient_neonatal|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Monogenic_diabetes|Diabetes_mellitus|_transient_neonatal|_1|ZFP57-related_disorder|Inborn_genetic_diseases": 1,
    "ZFP57-related_disorder|Diabetes_mellitus|_transient_neonatal|_1": 1,
    "Monogenic_diabetes|Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_1|not_specified|not_provided": 1,
    "not_provided|ZFP57-related_disorder": 1,
    "Diabetes_mellitus|_transient_neonatal|_1|ZFP57-related_disorder": 1,
    "Post-COVID-19_disorder": 1,
    "Susceptibility_to_severe_cutaneous_adverse_reaction": 2,
    "HLA-A-related_condition": 1,
    "Carbamazepine_hypersensitivity": 1,
    "not_provided|DHX16-related_disorder": 2,
    "Inborn_genetic_diseases|Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures": 2,
    "Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures": 23,
    "Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures|Inborn_genetic_diseases": 3,
    "DHX16-related_disorder": 14,
    "Multiple_renal_cysts|Reduced_renal_corticomedullary_differentiation|Enlarged_kidney|Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures|Neurodevelopmental_disorders": 1,
    "not_provided|Neurodevelopmental_disorders|Intellectual_disability|Neurodevelopmental_delay|Seizure|Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "Seizure|Neurodevelopmental_delay|Periventricular_heterotopia|Chorioretinal_lacunae|Corpus_callosum|_agenesis_of|Intellectual_disability|Neurodevelopmental_disorders|Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures": 1,
    "Neurodevelopmental_delay|Intellectual_disability|Neurodevelopmental_disorders|Neuromuscular_disease_and_ocular_or_auditory_anomalies_with_or_without_seizures": 1,
    "DHX16-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|DHX16-related_disorder|not_provided": 1,
    "DHX16-related_disorder|not_specified|not_provided": 1,
    "Multiple_benign_circumferential_skin_creases_on_limbs_1": 3,
    "TUBB-related_disorder": 2,
    "Complex_cortical_dysplasia_with_other_brain_malformations_6": 14,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_6": 6,
    "Complex_cortical_dysplasia_with_other_brain_malformations_6|Multiple_benign_circumferential_skin_creases_on_limbs_1": 2,
    "Complex_cortical_dysplasia_with_other_brain_malformations_6|Inborn_genetic_diseases|Multiple_benign_circumferential_skin_creases_on_limbs_1": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_6|not_provided": 1,
    "Multiple_benign_circumferential_skin_creases_on_limbs_1|Complex_cortical_dysplasia_with_other_brain_malformations_6": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_6|not_provided|Inborn_genetic_diseases": 1,
    "Multiple_benign_circumferential_skin_creases_on_limbs_1|not_provided": 1,
    "TUBB-related_tubulinopathy": 1,
    "TUBB-related_disorder|not_provided": 1,
    "Multiple_benign_circumferential_skin_creases_on_limbs_1|Seizure|Complex_cortical_dysplasia_with_other_brain_malformations_6|not_provided|Lissencephaly": 1,
    "Inborn_genetic_diseases|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_6": 1,
    "Abnormal_brain_morphology|Inborn_genetic_diseases|Complex_cortical_dysplasia_with_other_brain_malformations_6": 1,
    "TUBB-related_disorder|Multiple_benign_circumferential_skin_creases_on_limbs_1|Complex_cortical_dysplasia_with_other_brain_malformations_6": 1,
    "Ventriculomegaly|Hypoplasia_of_the_corpus_callosum": 1,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_6|Inborn_genetic_diseases|Multiple_benign_circumferential_skin_creases_on_limbs_1": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_20|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_20": 29,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_20": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_20": 7,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_20|not_provided": 4,
    "not_provided|VARS2-related_disorder": 5,
    "VARS2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_20|not_provided": 6,
    "Inborn_genetic_diseases|not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_20": 1,
    "Combined_oxidative_phosphorylation_defect_type_20|not_specified|not_provided": 4,
    "VARS2-related_disorder|not_provided": 3,
    "not_provided|VARS2-related_disorder|not_specified": 1,
    "VARS2-related_disorder": 4,
    "not_specified|not_provided|VARS2-related_disorder": 1,
    "VARS2-related_disorder|not_provided|See_cases|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_20": 1,
    "not_provided|not_specified|VARS2-related_disorder": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_20": 2,
    "Combined_oxidative_phosphorylation_defect_type_20|Inborn_genetic_diseases|not_provided|See_cases": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_20|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_20": 1,
    "not_provided|VARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_20": 1,
    "Inborn_genetic_diseases|not_provided|VARS2-related_disorder": 1,
    "VARS2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_20|Inborn_genetic_diseases": 1,
    "MUC21-related_disorder|not_provided": 1,
    "Serum_phosphorus_normal_or_mildly_elevated": 1,
    "Peeling_skin_syndrome_1|not_provided": 2,
    "CDSN-related_disorder|not_provided": 7,
    "Peeling_skin_syndrome_1|Hypotrichosis_2|not_provided": 1,
    "Peeling_skin_syndrome_1": 8,
    "not_provided|CDSN-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|CDSN-related_disorder": 2,
    "Peeling_skin_syndrome_1|CDSN-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Hypotrichosis_2|not_provided": 1,
    "not_provided|CDSN-related_disorder": 3,
    "CDSN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Hypotrichosis_2": 2,
    "CDSN-related_disorder": 1,
    "Hypotrichosis_2|not_provided|CDSN-related_disorder": 1,
    "not_provided|Peeling_skin_syndrome_1": 1,
    "PSORS1C1-related_disorder": 6,
    "not_provided|PSORS1C1-related_disorder": 1,
    "HIV-1_VIREMIA|_SUSCEPTIBILITY_TO": 1,
    "Spondyloarthropathy|_susceptibility_to|_1": 1,
    "HLA-B-related_disorder": 13,
    "Abacavir_hypersensitivity|Autism_spectrum_disorder": 1,
    "NFKBIL1-related_disorder": 4,
    "Leprosy|_early-onset|_susceptibility_to": 1,
    "Psoriatic_arthritis|_susceptibility_to|Myocardial_infarction|_susceptibility_to": 1,
    "LTA-related_disorder": 2,
    "LTA-related_disorder|Myocardial_infarction|_susceptibility_to": 1,
    "Alzheimer_disease|_protection_against": 1,
    ".|.": 1,
    "Malaria|_cerebral|_susceptibility_to": 1,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)|HUMAN_IMMUNODEFICIENCY_VIRUS_DEMENTIA|_SUSCEPTIBILITY_TO|.|Psoriatic_arthritis|_susceptibility_to|Malaria|_cerebral|_susceptibility_to|.|etanercept_response_-_Efficacy|Endometriosis|Systemic_lupus_erythematosus|_susceptibility_to|Inherited_susceptibility_to_asthma|Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_plasma_levels_of_TNF|_TNFR|_and/or_TNFR4": 1,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_plasma_levels_of_TNF|_TNFR|_and/or_TNFR5|Susceptibility_to_severe_coronavirus_disease_(COVID-19)": 1,
    "Migraine_with_or_without_aura|_susceptibility_to|_1": 1,
    "Increased_circulating_interleukin_6_concentration": 1,
    "Migraine_with_or_without_aura|_susceptibility_to|_1|Inherited_susceptibility_to_asthma": 1,
    "TNF_receptor_binding|_altered": 1,
    "NCR3-related_disorder": 2,
    "not_provided|NCR3-related_disorder": 2,
    "Malaria|_severe|_susceptibility_to": 1,
    "Malaria|_severe|_susceptibility_to|Malaria|_mild|_susceptibility_to": 1,
    "PRRC2A-related_disorder": 62,
    "not_provided|PRRC2A-related_disorder": 6,
    "not_specified|PRRC2A-related_disorder": 1,
    "Cerebellar_vermis_hypoplasia|Periventricular_nodular_heterotopia|Isolated_unilateral_hemispheric_cerebellar_hypoplasia": 1,
    "CSNK2B-related_disorder": 9,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|not_provided": 5,
    "not_provided|Poirier-Bienvenu_neurodevelopmental_syndrome": 12,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_non-syndromic_intellectual_disability|Poirier-Bienvenu_neurodevelopmental_syndrome": 1,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "Deeply_set_eye|Pointed_chin|Mandibular_prognathia|Abnormal_facial_shape|Seizure|Asymmetry_of_the_ears|Underdeveloped_nasal_alae|Intellectual_disability|Thin_upper_lip_vermilion|Tapered_finger|Syndactyly|Toe_clinodactyly|Poirier-Bienvenu_neurodevelopmental_syndrome|CSNK2B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability-craniodigital_syndrome": 1,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|Intellectual_disability_and_seizures": 1,
    "not_provided|Inborn_genetic_diseases|Poirier-Bienvenu_neurodevelopmental_syndrome": 1,
    "CSNK2B-related_disorder|Poirier-Bienvenu_neurodevelopmental_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|CSNK2B-related_disorder": 1,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "CSNK2B-related_intellectual_disability_with_or_without_epilepsy": 1,
    "Intellectual_disability|Seizure|Developmental_delay|Poirier-Bienvenu_neurodevelopmental_syndrome|not_provided": 1,
    "Neurodevelopmental_disorder|Poirier-Bienvenu_neurodevelopmental_syndrome": 1,
    "Inborn_genetic_diseases|Poirier-Bienvenu_neurodevelopmental_syndrome": 1,
    "Neurodevelopmental_disorder|Poirier-Bienvenu_neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "Poirier-Bienvenu_neurodevelopmental_syndrome|not_provided|See_cases": 1,
    "ABHD16A-related_disorder": 3,
    "Autosomal_recessive_complex_spastic_paraplegia": 1,
    "Spastic_paraplegia_86|_autosomal_recessive|Complex_hereditary_spastic_paraplegia": 2,
    "Spastic_paraplegia_86|_autosomal_recessive": 3,
    "Spastic_paraplegia|Spastic_paraplegia_86|_autosomal_recessive": 3,
    "Thrombocythemia_2|not_provided": 1,
    "Thrombocytopenia|_anemia|_and_myelofibrosis": 9,
    "not_provided|Thrombocytopenia|_anemia|_and_myelofibrosis": 3,
    "MPIG6B-related_disorder": 2,
    "not_provided|MPIG6B-related_disorder": 4,
    "Thrombocytopenia|_anemia|_and_myelofibrosis|not_provided": 1,
    "Non-obstructive_azoospermia|Spermatogenic_failure_74": 3,
    "MSH5-related_disorder|not_specified": 1,
    "MSH5-related_disorder": 5,
    "not_provided|MSH5-related_disorder": 2,
    "Premature_ovarian_failure_13": 3,
    "Spermatogenic_failure_74|Premature_ovarian_failure_13|MSH5-related_disorder|not_provided|Genetic_non-acquired_premature_ovarian_failure": 1,
    "MSH5-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy": 55,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy|not_provided": 3,
    "VARS1-related_disorder": 9,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy|Inborn_genetic_diseases": 8,
    "VARS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|VARS1-related_disorder": 4,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy|not_provided|Microcephaly|Elevated_circulating_hepatic_transaminase_concentration|Intellectual_disability|Generalized_hypotonia|Delayed_speech_and_language_development|Premature_birth": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy|Abnormal_brain_morphology": 1,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy": 1,
    "Abnormal_brain_morphology|Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy": 1,
    "Inborn_genetic_diseases|VARS1-related_disorder": 1,
    "VARS1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy": 2,
    "Intellectual_disability|Secondary_microcephaly|Generalized_hypotonia|Elevated_circulating_hepatic_transaminase_concentration|Delayed_speech_and_language_development|Premature_birth": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_cortical_atrophy|not_provided|Inborn_genetic_diseases": 1,
    "HSPA1L-related_disorder": 11,
    "HSPA1L-related_disorder|not_provided": 2,
    "Inflammatory_bowel_disease_1|not_provided|HSPA1L-related_disorder": 1,
    "not_provided|HSPA1L-related_disorder": 4,
    "Inflammatory_bowel_disease_1|HSPA1L-related_disorder|not_provided": 1,
    "Inflammatory_bowel_disease_1": 4,
    "Sialidosis_type_2": 28,
    "Sialidosis_type_2|not_provided": 10,
    "not_provided|Sialidosis_type_2": 13,
    "NEU1-related_disorder|not_provided": 3,
    "NEU1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "NEU1-related_disorder": 3,
    "Non-immune_hydrops_fetalis|Sialidosis_type_2": 2,
    "Sialidosis_type_1": 2,
    "not_provided|Sialidosis|Sialidosis_type_2": 1,
    "Sialidosis": 1,
    "Sialidosis|not_provided": 6,
    "not_provided|Sialidosis": 3,
    "not_provided|NEU1-related_disorder": 3,
    "not_specified|not_provided|Sialidosis_type_2": 1,
    "Sialidosis_type_2|not_provided|Sialidosis": 1,
    "not_provided|Sialidosis_type_1": 1,
    "Sialidosis|not_provided|Sialidosis_type_2": 1,
    "Sialidosis_type_1|not_provided|NEU1-related_disorder|Sialidosis": 1,
    "not_provided|NEU1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Sialidosis_type_2": 1,
    "not_provided|Sialidosis_type_2|not_specified": 1,
    "not_specified|Sialidosis_type_2": 1,
    "not_provided|Sialidosis_type_2|NEU1-related_disorder": 1,
    "SLC44A4-related_disorder|not_provided": 4,
    "not_provided|Hearing_loss|_autosomal_dominant_72": 7,
    "Hearing_loss|_autosomal_dominant_72": 2,
    "Hearing_loss|_autosomal_dominant_72|not_provided|not_specified": 1,
    "SLC44A4-related_disorder": 5,
    "not_provided|SLC44A4-related_disorder": 4,
    "SLC44A4-related_disorder|not_specified|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_72|not_provided": 2,
    "Kleefstra-like_syndrome": 6,
    "C2-related_disorder|ZBTB12-related_disorder": 1,
    "Age_related_macular_degeneration_14|Complement_component_2_deficiency": 13,
    "Complement_component_2_deficiency": 7,
    "Age_related_macular_degeneration_14|Complement_component_2_deficiency|not_provided": 3,
    "Complement_component_2_deficiency|not_provided|Macular_degeneration": 1,
    "Age_related_macular_degeneration_14|not_provided|Complement_component_2_deficiency": 5,
    "not_specified|Complement_component_2_deficiency|Age_related_macular_degeneration_14|not_provided": 1,
    "Complement_component_2_deficiency|not_provided": 1,
    "not_specified|Age_related_macular_degeneration_14|Complement_component_2_deficiency|not_provided": 1,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14": 5,
    "not_provided|Complement_component_2_deficiency|Age_related_macular_degeneration_14": 2,
    "not_provided|Age_related_macular_degeneration_14|Complement_component_2_deficiency": 4,
    "C2-related_disorder": 1,
    "C2_deficiency|_type_II": 1,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14|not_provided": 2,
    "not_provided|Complement_component_2_deficiency": 2,
    "C2-related_disorder|Age_related_macular_degeneration_14|Complement_component_2_deficiency|not_provided|C2_deficiency|_type_I": 1,
    "C2-related_disorder|not_provided": 2,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14|not_provided|not_specified": 1,
    "not_specified|Complement_component_2_deficiency|not_provided|Age_related_macular_degeneration_14": 1,
    "Age_related_macular_degeneration_14|not_provided|not_specified|Complement_component_2_deficiency": 1,
    "not_specified|not_provided|Age_related_macular_degeneration_14|Complement_component_2_deficiency": 1,
    "C2-related_disorder|not_specified|not_provided|Age_related_macular_degeneration_14|Complement_component_2_deficiency": 1,
    "Age_related_macular_degeneration_14": 1,
    "C2_deficiency|_type_II|not_provided": 1,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome|not_provided|Macular_degeneration": 1,
    "not_provided|Complement_component_2_deficiency|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome|Macular_degeneration": 5,
    "Age_related_macular_degeneration_14|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_specified|not_provided|Macular_degeneration": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Complement_component_2_deficiency|Age_related_macular_degeneration_14|C2-related_disorder": 1,
    "Age_related_macular_degeneration_14|not_provided|Macular_degeneration|Complement_component_2_deficiency": 1,
    "not_provided|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome|Macular_degeneration|not_specified|Age_related_macular_degeneration_14": 1,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14|not_provided|Atypical_hemolytic-uremic_syndrome|Macular_degeneration|C2-related_disorder": 1,
    "Complement_component_2_deficiency|not_specified|Age_related_macular_degeneration_14|not_provided": 1,
    "Complement_component_2_deficiency|not_provided|Age_related_macular_degeneration_14": 1,
    "Age_related_macular_degeneration_14|not_specified|Complement_component_2_deficiency|not_provided": 1,
    "Age_related_macular_degeneration_14|Macular_degeneration|Complement_component_2_deficiency": 1,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14|Macular_degeneration": 1,
    "Complement_component_2_deficiency|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome|Macular_degeneration": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration": 5,
    "Macular_degeneration|Atypical_hemolytic-uremic_syndrome": 1,
    "Complement_factor_b_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Age_related_macular_degeneration_14|Macular_degeneration": 1,
    "CFB-related_disorder|Complement_factor_b_deficiency|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_specified|not_provided|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome|Macular_degeneration": 1,
    "CFB-related_disorder|not_provided": 2,
    "CFB-related_disorder|Complement_factor_b_deficiency|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome|Factor_B_fast/slow_polymorphism|Focal_segmental_glomerulosclerosis|Macular_degeneration": 1,
    "Age_related_macular_degeneration_14|Complement_component_2_deficiency|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Factor_B_fast/slow_polymorphism|BF*FA/S|Focal_segmental_glomerulosclerosis|Macular_degeneration": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 3,
    "Complement_factor_b_deficiency": 3,
    "CFB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Complement_component_2_deficiency|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Inborn_genetic_diseases|not_provided|Macular_degeneration": 1,
    "CFB-related_disorder|not_provided|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 1,
    "not_provided|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 6,
    "Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 4,
    "Complement_component_2_deficiency|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|CFB-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|CFB-related_disorder": 4,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided": 1,
    "Complement_component_2_deficiency|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Complement_factor_b_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 2,
    "CFB-related_disorder|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome|not_provided|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided": 1,
    "Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Complement_factor_b_deficiency|not_provided|not_specified": 1,
    "not_specified|Kidney_disorder|Complement_component_2_deficiency|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Macular_degeneration": 1,
    "not_specified|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_2_deficiency|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|CFB-related_disorder|not_provided": 1,
    "Complement_factor_b_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|CFB-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 2,
    "Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome|not_provided|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_specified": 1,
    "CFB-related_disorder": 1,
    "not_specified|not_provided|Kidney_disorder": 3,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration|CFB-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome": 2,
    "Complement_factor_b_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome|not_provided|Complement_component_2_deficiency|Macular_degeneration|not_specified|Kidney_disorder|CFB-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_2_deficiency|CFB-related_disorder|Macular_degeneration|Inborn_genetic_diseases|not_provided|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly": 1,
    "not_specified|Complement_component_2_deficiency|Focal_segmental_glomerulosclerosis|Macular_degeneration|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|CFB-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Complement_factor_b_deficiency|Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome|not_specified|not_provided": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration": 2,
    "not_provided|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration|not_provided|CFB-related_disorder": 1,
    "Age_related_macular_degeneration_14|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Complement_factor_b_deficiency|Atypical_hemolytic-uremic_syndrome|Macular_degeneration|Complement_component_2_deficiency|not_specified|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Complement_factor_b_deficiency|not_provided": 1,
    "CFB-related_disorder|Macular_degeneration|Complement_factor_b_deficiency|not_provided|Complement_component_2_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Kidney_disorder|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration|not_provided": 1,
    "Age_related_macular_degeneration_14|Complement_factor_b_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|CFB-related_disorder|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration": 1,
    "Macular_degeneration|Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Inborn_genetic_diseases": 1,
    "Complement_factor_b_deficiency|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Macular_degeneration": 1,
    "Complement_factor_b_deficiency|Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Age_related_macular_degeneration_14|not_provided|Macular_degeneration|CFB-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome|Complement_factor_b_deficiency": 1,
    "Atypical_hemolytic-uremic_syndrome_with_B_factor_anomaly|Macular_degeneration|Atypical_hemolytic-uremic_syndrome": 1,
    "Trichohepatoenteric_syndrome_2": 28,
    "Trichohepatoenteric_syndrome_2|not_provided": 20,
    "not_provided|Trichohepatoenteric_syndrome_2": 39,
    "Trichohepatoenteric_syndrome_2|not_provided|Trichohepatoenteric_syndrome": 1,
    "not_provided|SKIC2-related_disorder": 5,
    "not_provided|not_specified|Trichohepatoenteric_syndrome_2": 4,
    "SKIC2-related_disorder|not_provided|Trichohepatoenteric_syndrome_2": 3,
    "not_provided|SKIC2-related_disorder|Trichohepatoenteric_syndrome_2": 2,
    "SKIC2-related_disorder": 6,
    "not_provided|Trichohepatoenteric_syndrome_2|not_specified": 1,
    "SKIC2-related_disorder|not_provided": 3,
    "Trichohepatoenteric_syndrome_2|not_specified": 1,
    "not_provided|Trichohepatoenteric_syndrome_2|Inborn_genetic_diseases": 3,
    "SKIC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Trichohepatoenteric_syndrome_2": 2,
    "not_provided|Trichohepatoenteric_syndrome_2|SKIC2-related_disorder": 2,
    "SKIC2-related_disorder|Trichohepatoenteric_syndrome_2|See_cases|not_provided": 1,
    "Trichohepatoenteric_syndrome_2|not_provided|SKIC2-related_disorder": 1,
    "Trichohepatoenteric_syndrome_2|Inborn_genetic_diseases": 2,
    "Trichohepatoenteric_syndrome|not_provided|SKIC2-related_disorder|Trichohepatoenteric_syndrome_2": 1,
    "Trichohepatoenteric_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Complement_component_4a_deficiency": 3,
    "Complement_component_4a_deficiency|not_provided": 1,
    "not_specified|Complement_component_4b_deficiency": 1,
    "Complement_component_4b_deficiency": 3,
    "CYP21A2-related_disorder|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 3,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 136,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_provided|Congenital_adrenal_hyperplasia": 2,
    "CYP21A2-related_disorder": 14,
    "21-HYDROXYLASE_POLYMORPHISM|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_provided|not_specified": 1,
    "not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 17,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_specified|not_provided": 2,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_specified": 2,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_provided": 12,
    "not_specified|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|Congenital_adrenal_hyperplasia": 1,
    "Congenital_adrenal_hyperplasia|CYP21A2-related_disorder": 1,
    "not_provided|CYP21A2-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Congenital_adrenal_hyperplasia|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|See_cases": 1,
    "CYP21A2-related_disorder|not_provided|Congenital_adrenal_hyperplasia|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 2,
    "not_specified|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 4,
    "not_specified|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_provided": 1,
    "not_specified|Congenital_adrenal_hyperplasia|not_provided": 1,
    "not_specified|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 5,
    "not_provided|not_specified|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 2,
    "Inborn_genetic_diseases|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_adrenal_hyperplasia|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|Congenital_adrenal_hyperplasia|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Congenital_adrenal_hyperplasia|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_specified": 3,
    "not_specified|not_provided|Congenital_adrenal_hyperplasia|21-HYDROXYLASE_POLYMORPHISM|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "CYP21A2-related_disorder|Inborn_genetic_diseases|not_provided|Congenital_adrenal_hyperplasia|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|Adenoma|_cortisol-producing|Carcinoma|_adrenocortical|_androgen-secreting": 1,
    "CYP21A2-related_disorder|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 3,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|Hyperandrogenism|_nonclassic_type|_due_to_21-hydroxylase_deficiency": 1,
    "CYP21A2-related_disorder|not_provided": 2,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|CYP21A2-related_disorder": 1,
    "not_provided|CYP21A2-related_disorder|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Hyperandrogenism|_nonclassic_type|_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|CYP21A2-related_disorder": 1,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|CYP21A2-related_disorder|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|See_cases": 1,
    "not_provided|Congenital_adrenal_hyperplasia|CYP21A2-related_disorder|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|not_specified|CYP21A2-related_disorder|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 46,
    "Vesicoureteral_reflux_8": 18,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided": 3,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 51,
    "not_specified|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "TNXB-related_disorder|not_provided|Vesicoureteral_reflux_8": 1,
    "Vesicoureteral_reflux_8|not_provided": 2,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|TNXB-related_disorder": 2,
    "TNXB-related_disorder": 21,
    "not_provided|not_specified|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "TNXB-related_disorder|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|TNXB-related_disorder|not_provided": 1,
    "Vesicoureteral_reflux_8|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_specified|Cardiovascular_phenotype": 2,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|TNXB-related_disorder": 1,
    "Cardiovascular_phenotype|TNXB-related_disorder": 17,
    "not_specified|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|not_provided": 1,
    "Vesicoureteral_reflux_8|not_provided|not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 7,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_specified|Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Ehlers-Danlos_syndrome": 1,
    "TNXB-related_disorder|not_provided": 2,
    "not_specified|not_provided|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "not_specified|TNXB-related_disorder|not_provided|Cardiovascular_phenotype": 2,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype": 9,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_specified": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided": 13,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|not_provided": 2,
    "TNXB-related_disorder|Cardiovascular_phenotype|not_provided": 8,
    "not_specified|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 2,
    "TNXB-related_disorder|Cardiovascular_phenotype": 11,
    "See_cases|Cardiovascular_phenotype": 2,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype": 7,
    "Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype": 17,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 2,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 2,
    "Ehlers-Danlos_syndrome|not_provided|TNXB-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Vesicoureteral_reflux_8": 1,
    "not_provided|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 3,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 9,
    "TNXB-related_disorder|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|not_specified": 2,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided": 4,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 3,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|See_cases": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Vesicoureteral_reflux_8|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Vesicoureteral_reflux_8|not_provided": 1,
    "not_specified|not_provided|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|TNXB-related_disorder": 1,
    "not_specified|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 2,
    "not_specified|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided": 3,
    "not_specified|not_provided|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 4,
    "TNXB-related_disorder|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|TNXB-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "TNXB-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|TNXB-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Ehlers-Danlos_syndrome|not_specified|TNXB-related_disorder|Cardiovascular_phenotype": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|TNXB-related_disorder": 4,
    "not_provided|Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype": 5,
    "not_provided|TNXB-related_disorder": 2,
    "not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|TNXB-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 7,
    "Cardiovascular_phenotype|not_provided|TNXB-related_disorder|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|Vesicoureteral_reflux_8|Cardiovascular_phenotype|TNXB-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Vesicoureteral_reflux_8": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|TNXB-related_disorder|Ehlers-Danlos_syndrome|not_provided": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 3,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided|TNXB-related_disorder|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|TNXB-related_disorder|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 2,
    "not_specified|Cardiovascular_phenotype|TNXB-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 3,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided": 3,
    "TNXB-related_disorder|not_provided|Cardiovascular_phenotype": 3,
    "not_provided|Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype|Vesicoureteral_reflux_8": 1,
    "Ehlers-Danlos_syndrome|TNXB-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|TNXB-related_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided|Cardiovascular_phenotype": 1,
    "TNXB-related_hypermobile_Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|TNXB-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Vesicoureteral_reflux_8": 1,
    "not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided|Cardiovascular_phenotype": 4,
    "not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|not_provided": 5,
    "Cardiovascular_phenotype|not_provided|not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided": 2,
    "Vesicoureteral_reflux_8|not_specified|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 3,
    "not_specified|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype": 1,
    "not_specified|TNXB-related_disorder|Cardiovascular_phenotype": 1,
    "TNXB-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Vesicoureteral_reflux_8": 4,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|TNXB-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Vesicoureteral_reflux_8|not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 3,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified": 2,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 4,
    "TNXB-related_disorder|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 1,
    "not_specified|Vesicoureteral_reflux_8|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 1,
    "TNXB-related_disorder|Cardiovascular_phenotype|not_specified": 4,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|TNXB-related_disorder|not_specified|Cardiovascular_phenotype|Vesicoureteral_reflux_8|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "Cardiovascular_phenotype|TNXB-related_disorder|not_provided": 4,
    "Dyskeratosis_congenita|_autosomal_dominant_3": 8,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_specified|not_provided": 1,
    "TNXB-related_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "Breathing_dysregulation|Myoclonus|Dyspnea|Neonatal_breathing_dysregulation|Abnormal_pattern_of_respiration|Cyanosis|Hypotonia|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "TNXB-related_disorder|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided": 1,
    "Vesicoureteral_reflux_8|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|TNXB-related_disorder|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|TNXB-related_disorder|Cardiovascular_phenotype|Vesicoureteral_reflux_8": 1,
    "not_provided|TNXB-related_disorder|Cardiovascular_phenotype": 4,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_type_3": 1,
    "Cardiovascular_phenotype|TNXB-related_disorder|Ehlers-Danlos_syndrome": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 1,
    "not_specified|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided|TNXB-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 2,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Vesicoureteral_reflux_8|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "Breathing_dysregulation|Myoclonus|Dyspnea|Neonatal_breathing_dysregulation|Abnormal_pattern_of_respiration|Cyanosis|Hypotonia|Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 1,
    "not_provided|not_specified|TNXB-related_disorder|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided|Ehlers-Danlos_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_specified": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "TNXB-related_disorder|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Vesicoureteral_reflux_8|Cardiovascular_phenotype": 1,
    "Vesicoureteral_reflux_8|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|TNXB-related_disorder": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome": 2,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|Vesicoureteral_reflux_8": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "TNXB-related_disorder|not_specified|See_cases|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome": 1,
    "TNXB-related_disorder|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|Vesicoureteral_reflux_8|Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_specified|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|not_provided|TNXB-related_disorder": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|not_specified|not_provided|Ehlers-Danlos_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|TNXB-related_disorder|See_cases": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_type_3": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|TNXB-related_disorder": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "TNXB-related_disorder|Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8": 1,
    "Vesicoureteral_reflux_8|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided": 1,
    "not_provided|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Inborn_genetic_diseases": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|not_provided|not_specified|Vesicoureteral_reflux_8": 1,
    "Vesicoureteral_reflux_8|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|TNXB-related_disorder|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_specified|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency": 1,
    "Cardiovascular_phenotype|not_provided|Vesicoureteral_reflux_8": 1,
    "not_provided|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Cardiovascular_phenotype|TNXB-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|not_provided": 1,
    "Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Vesicoureteral_reflux_8|Ehlers-Danlos_syndrome_due_to_tenascin-X_deficiency|Cardiovascular_phenotype|TNXB-related_disorder|Ehlers-Danlos_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|TNXB-related_disorder|not_provided|not_specified": 1,
    "FKBPL-related_disorder": 6,
    "COPD|_severe_early_onset": 4,
    "Anophthalmia-microphthalmia_syndrome|not_provided": 9,
    "Sarcoidosis|_susceptibility_to|_2": 1,
    "BTNL2-related_condition": 1,
    "Multiple_sclerosis|_susceptibility_to": 6,
    "HLA-DRB1-related_disorder": 5,
    "TAP2-related_disorder": 2,
    "not_specified|TAP2-related_disorder": 1,
    "MHC_class_I_deficiency": 932,
    "MHC_class_I_deficiency|not_specified": 19,
    "TAP2_POLYMORPHISM|MHC_class_I_deficiency": 2,
    "Inborn_genetic_diseases|MHC_class_I_deficiency": 47,
    "MHC_class_I_deficiency|TAP2-related_disorder": 8,
    "MHC_class_I_deficiency|Inborn_genetic_diseases": 28,
    "MHC_class_I_deficiency|not_provided": 12,
    "not_specified|MHC_class_I_deficiency": 17,
    "TAP2-related_disorder|MHC_class_I_deficiency|not_specified": 1,
    "MHC_class_I_deficiency|not_specified|not_provided": 6,
    "not_provided|MHC_class_I_deficiency": 15,
    "Inborn_genetic_diseases|MHC_class_I_deficiency|MHC_class_I_deficiency_1": 1,
    "MHC_class_I_deficiency|not_provided|TAP2-related_disorder": 1,
    "not_provided|MHC_class_I_deficiency|not_specified": 1,
    "TAP2-related_disorder|MHC_class_I_deficiency": 7,
    "TAP2_POLYMORPHISM|not_specified|not_provided|MHC_class_I_deficiency": 1,
    "MHC_class_I_deficiency|TAP2-related_disorder|not_provided": 1,
    "MHC_class_I_deficiency_2": 2,
    "not_provided|MHC_class_I_deficiency|MHC_class_I_deficiency_1": 1,
    "MHC_class_I_deficiency|MHC_class_I_deficiency_2": 1,
    "TAP2-related_disorder|not_provided": 1,
    "TAP2-related_disorder|MHC_class_I_deficiency|not_provided": 1,
    "not_provided|Proteasome-associated_autoinflammatory_syndrome_1|Autoinflammatory_syndrome": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Autoinflammatory_syndrome|not_specified": 1,
    "Proteosome-associated_autoinflammatory_syndrome": 129,
    "Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome|Autoinflammatory_syndrome|not_provided": 1,
    "not_specified|Proteosome-associated_autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Proteosome-associated_autoinflammatory_syndrome": 3,
    "Inborn_genetic_diseases|Proteosome-associated_autoinflammatory_syndrome": 4,
    "Autoinflammatory_syndrome|Proteasome-associated_autoinflammatory_syndrome_1|Inborn_genetic_diseases": 1,
    "Proteosome-associated_autoinflammatory_syndrome|PSMB8-related_disorder|not_provided|Proteasome-associated_autoinflammatory_syndrome_1|Autoinflammatory_syndrome": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Inborn_genetic_diseases": 3,
    "Autoinflammatory_syndrome|Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome": 2,
    "Proteosome-associated_autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Proteosome-associated_autoinflammatory_syndrome|not_provided": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome": 2,
    "Proteasome-associated_autoinflammatory_syndrome_1|not_provided": 2,
    "Proteosome-associated_autoinflammatory_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Proteasome-associated_autoinflammatory_syndrome_1": 2,
    "not_provided|Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome": 2,
    "PSMB8-related_disorder": 3,
    "not_specified|Autoinflammatory_syndrome|Proteosome-associated_autoinflammatory_syndrome|not_provided|Proteasome-associated_autoinflammatory_syndrome_1": 1,
    "Autoinflammatory_syndrome|Proteosome-associated_autoinflammatory_syndrome|not_provided|Proteasome-associated_autoinflammatory_syndrome_1": 2,
    "Proteosome-associated_autoinflammatory_syndrome|Autoinflammatory_syndrome": 3,
    "Proteasome-associated_autoinflammatory_syndrome_1|not_provided|Proteosome-associated_autoinflammatory_syndrome|not_specified": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Autoinflammatory_syndrome": 1,
    "Proteosome-associated_autoinflammatory_syndrome|PSMB8-related_disorder": 2,
    "not_provided|Proteasome-associated_autoinflammatory_syndrome_1": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome|PSMB8-related_disorder|PROTEASOME-ASSOCIATED_AUTOINFLAMMATORY_SYNDROME_1|_DIGENIC|not_provided": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome|Autoinflammatory_syndrome": 2,
    "Autoinflammatory_syndrome|not_provided|Proteosome-associated_autoinflammatory_syndrome|not_specified|Proteasome-associated_autoinflammatory_syndrome_1": 1,
    "Proteasome-associated_autoinflammatory_syndrome_1|Autoinflammatory_syndrome|Proteosome-associated_autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|Proteasome-associated_autoinflammatory_syndrome_1|Proteosome-associated_autoinflammatory_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Proteasome-associated_autoinflammatory_syndrome_1": 1,
    "Proteosome-associated_autoinflammatory_syndrome|Proteasome-associated_autoinflammatory_syndrome_1|See_cases": 1,
    "MHC_class_I_deficiency_1": 2,
    "TAP1-related_disorder|MHC_class_I_deficiency": 1,
    "TAP1_deficiency|_somatic|MHC_class_I_deficiency|not_provided": 1,
    "not_specified|PEPTIDE_TRANSPORTER_PSF1_POLYMORPHISM|MHC_class_I_deficiency": 1,
    "MHC_class_I_deficiency_1|MHC_class_I_deficiency": 1,
    "MHC_class_I_deficiency|TAP1-related_disorder": 4,
    "not_provided|MHC_class_I_deficiency|TAP1-related_disorder": 1,
    "MHC_class_I_deficiency|MHC_class_I_deficiency_1": 3,
    "MHC_class_I_deficiency|not_provided|TAP1-related_disorder": 1,
    "PEPTIDE_TRANSPORTER_PSF1_POLYMORPHISM|MHC_class_I_deficiency|not_specified": 1,
    "TAP1-related_disorder|MHC_class_I_deficiency|not_provided": 1,
    "MHC_class_I_deficiency|not_provided|not_specified": 2,
    "TAP1-related_disorder|not_provided|MHC_class_I_deficiency": 1,
    "Proteasome-associated_autoinflammatory_syndrome_6": 1,
    "PSMB9-related_disorder": 7,
    "PSMB9-related_disorder|Proteasome-associated_autoinflammatory_syndrome_3|not_specified": 1,
    "Proteasome-associated_autoinflammatory_syndrome_6|proteasome-associated_autoinflammatory_syndrome_with_immunodeficiency_(PRAAS-ID)": 1,
    "not_specified|PSMB9-related_disorder": 1,
    "Proteasome-associated_autoinflammatory_syndrome_3|not_specified": 1,
    "PSMB9-related_disorder|not_provided": 1,
    "not_provided|BRD2-related_disorder": 5,
    "BRD2-related_disorder": 8,
    "BRD2-related_disorder|not_provided": 5,
    "BRD2-related_disorder|not_specified": 1,
    "Beryllium_disease|_chronic|_susceptibility_to": 2,
    "Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2": 2,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 9,
    "Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 4,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 2,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 4,
    "Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 8,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided|Fibrochondrogenesis_2|Connective_tissue_disorder|not_specified|Stickler_Syndrome|_Dominant": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53": 1,
    "Connective_tissue_disorder|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant": 1,
    "COL11A2-related_disorder|not_specified|not_provided": 6,
    "COL11A2-related_disorder": 16,
    "not_provided|COL11A2-related_disorder": 25,
    "not_specified|not_provided|COL11A2-related_disorder": 6,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 3,
    "not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|Fibrochondrogenesis_2": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|not_provided|Fibrochondrogenesis_2": 1,
    "Stickler_Syndrome|_Dominant|Connective_tissue_disorder|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|COL11A2-related_disorder|Fibrochondrogenesis_2": 1,
    "Connective_tissue_disorder|Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13": 7,
    "not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|Fibrochondrogenesis_2": 1,
    "Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 4,
    "COL11A2-related_disorder|not_specified|not_provided|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|COL11A2-related_disorder|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|COL11A2-related_disorder|Connective_tissue_disorder|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|Stickler_Syndrome|_Dominant|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_1|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified": 1,
    "not_provided|not_specified|COL11A2-related_disorder": 5,
    "COL11A2-related_disorder|not_provided": 29,
    "not_specified|COL11A2-related_disorder|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Nonsyndromic_Hearing_Loss|_Dominant|Inborn_genetic_diseases|Fibrochondrogenesis_2|not_specified|Stickler_Syndrome|_Dominant|not_provided|Fibrochondrogenesis_1": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Connective_tissue_disorder|Stickler_Syndrome|_Dominant|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 3,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_specified|not_provided|Connective_tissue_disorder|Stickler_Syndrome|_Dominant|COL11A2-related_disorder": 1,
    "Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "not_provided|COL11A2-related_disorder|Connective_tissue_disorder": 1,
    "Stickler_Syndrome|_Dominant|COL11A2-related_disorder|not_provided|not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "COL11A2-related_disorder|Stickler_Syndrome|_Dominant|not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided": 2,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53": 1,
    "Stickler_Syndrome|_Dominant|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 7,
    "not_specified|Disproportionate_short-limb_short_stature|Abnormal_eyebrow_morphology|Conductive_hearing_impairment|Single_transverse_palmar_crease|Short_chin|Macrocephaly|Long_philtrum|Short_lingual_frenulum|Reduced_bone_mineral_density|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53": 11,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided": 2,
    "Connective_tissue_disorder|Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 2,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 8,
    "Connective_tissue_disorder|Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 2,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Stickler_Syndrome|_Dominant|not_provided": 1,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 4,
    "COL11A2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "COL11A2-related_disorder|Stickler_Syndrome|_Dominant|not_provided|not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided": 1,
    "Stickler_Syndrome|_Dominant|not_specified|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|COL11A2-related_disorder": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13": 7,
    "Stickler_Syndrome|_Dominant|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "not_specified|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant": 1,
    "not_provided|Inborn_genetic_diseases|COL11A2-related_disorder|Connective_tissue_disorder": 1,
    "not_provided|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_specified": 1,
    "not_provided|COL11A2-related_disorder|not_specified": 3,
    "COL11A2-related_disorder|not_provided|not_specified": 2,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_53": 1,
    "Connective_tissue_disorder|Nonsyndromic_genetic_hearing_loss|not_provided": 2,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 8,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 3,
    "not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|COL11A2-related_disorder|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided": 1,
    "not_provided|Oculodentodigital_dysplasia|_autosomal_recessive": 8,
    "not_specified|Connective_tissue_disorder|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_13": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|not_provided": 3,
    "Stickler_Syndrome|_Dominant|not_specified|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|COL11A2-related_disorder|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided": 1,
    "not_provided|not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Stickler_Syndrome|_Dominant|Inborn_genetic_diseases": 1,
    "not_provided|Down_syndrome|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "not_provided|Connective_tissue_disorder|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Fibrochondrogenesis_2": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_specified|not_provided": 1,
    "Intellectual_disability|Autosomal_dominant_nonsyndromic_hearing_loss_13|not_provided": 1,
    "COL11A2-related_disorder|Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|Stickler_Syndrome|_Dominant": 1,
    "Connective_tissue_disorder|Stickler_Syndrome|_Dominant|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided": 5,
    "Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13": 1,
    "not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|Stickler_Syndrome|_Dominant": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Fibrochondrogenesis_2|Stickler_Syndrome|_Dominant|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2": 1,
    "Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|Stickler_Syndrome|_Dominant": 1,
    "not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13": 1,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Fibrochondrogenesis_2": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Stickler_Syndrome|_Dominant": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided": 4,
    "not_provided|Connective_tissue_disorder|Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Fibrochondrogenesis_2": 1,
    "COL11A2-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_13|Rare_genetic_deafness|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|not_provided": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|not_specified|Connective_tissue_disorder": 1,
    "Fibrochondrogenesis_2": 4,
    "Stickler_Syndrome|_Dominant|Connective_tissue_disorder|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided": 2,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided|COL11A2-related_disorder|Fibrochondrogenesis_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|not_provided|Fibrochondrogenesis_2": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_specified": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|COL11A2-related_disorder|not_provided": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided|not_specified|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant": 2,
    "Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_1|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_provided|Connective_tissue_disorder|not_specified|Hearing_impairment": 1,
    "not_specified|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53": 2,
    "Connective_tissue_disorder|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2": 1,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_1|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Inborn_genetic_diseases|not_provided|COL11A2-related_disorder": 1,
    "Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Stickler_Syndrome|_Dominant|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided|Fibrochondrogenesis_2": 1,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|COL11A2-related_disorder": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|COL11A2-related_disorder|Connective_tissue_disorder|not_specified|not_provided": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided|Connective_tissue_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|COL11A2-related_disorder": 1,
    "Stickler_Syndrome|_Dominant|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided|not_specified": 1,
    "COL11A2-related_disorder|not_provided|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Hearing_impairment": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_13": 1,
    "Connective_tissue_disorder|COL11A2-related_disorder|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13|Fibrochondrogenesis_2|not_provided": 1,
    "COL11A2-related_disorder|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13|Hearing_impairment": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|not_specified": 1,
    "not_specified|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Stickler_Syndrome|_Dominant": 1,
    "Heart|_malformation_of|Cystic_hygroma|Thickened_nuchal_skin_fold|Short_long_bone": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|COL11A2-related_disorder|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_specified|Fibrochondrogenesis_1|Nonsyndromic_Hearing_Loss|_Dominant|Stickler_Syndrome|_Dominant|not_provided": 1,
    "COL11A2-related_disorder|Inborn_genetic_diseases|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Hearing_impairment": 1,
    "Connective_tissue_disorder|not_specified|Fibrochondrogenesis_2|not_provided|Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|not_provided|Connective_tissue_disorder|Stickler_Syndrome|_Dominant": 1,
    "not_specified|not_provided|Larsen-like_syndrome|_B3GAT3_type": 1,
    "COL11A2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_33|not_provided": 1,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_dominant_nonsyndromic_hearing_loss_13": 1,
    "Hearing_impairment|not_provided|Connective_tissue_disorder|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_13|Connective_tissue_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided": 1,
    "not_specified|Stickler_Syndrome|_Dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_53|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided|COL11A2-related_disorder": 1,
    "not_provided|Stickler_Syndrome|_Dominant|not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_specified|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_provided|Stickler_Syndrome|_Dominant": 1,
    "Stickler_Syndrome|_Dominant|not_specified|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "not_specified|COL11A2-related_disorder": 1,
    "not_provided|not_specified|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided": 1,
    "not_specified|Deafness|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided|Heart|_malformation_of|Short_long_bone|Thickened_nuchal_skin_fold|Cystic_hygroma|Ear_malformation": 1,
    "not_provided|Connective_tissue_disorder|not_specified|COL11A2-related_disorder": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_53|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|not_provided": 1,
    "Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Connective_tissue_disorder|COL11A2-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Fibrochondrogenesis_2|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "Connective_tissue_disorder|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Stickler_Syndrome|_Dominant|not_specified": 1,
    "COL11A2-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Stickler_Syndrome|_Dominant|not_specified": 1,
    "COL11A2-related_disorder|Stickler_Syndrome|_Dominant|Connective_tissue_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|COL11A2-related_disorder|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|COL11A2-related_disorder|Fibrochondrogenesis_2|not_provided": 1,
    "COL11A2-related_disorder|Inborn_genetic_diseases|Connective_tissue_disorder|not_specified|not_provided": 1,
    "not_provided|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|Autosomal_recessive_nonsyndromic_hearing_loss_53|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided": 1,
    "not_specified|COL11A2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|Autosomal_dominant_nonsyndromic_hearing_loss_13": 1,
    "Inborn_genetic_diseases|Stickler_Syndrome|_Dominant|Connective_tissue_disorder|not_specified|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Autosomal_recessive_nonsyndromic_hearing_loss_53|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Fibrochondrogenesis_2|not_provided": 1,
    "not_provided|Nonsyndromic_Deafness|Autosomal_recessive_nonsyndromic_hearing_loss_53": 1,
    "See_cases|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_53|not_provided": 1,
    "not_provided|Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|Autosomal_dominant_nonsyndromic_hearing_loss_13|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|not_provided": 1,
    "Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|not_specified|Fibrochondrogenesis_2": 1,
    "Stickler_Syndrome|_Dominant|not_provided|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant": 1,
    "Stickler_Syndrome|_Dominant|Fibrochondrogenesis_2|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive": 1,
    "Fibrochondrogenesis_1|not_provided|Otospondylomegaepiphyseal_dysplasia|_autosomal_dominant|Otospondylomegaepiphyseal_dysplasia|_autosomal_recessive|Nonsyndromic_Hearing_Loss|_Dominant|Stickler_Syndrome|_Dominant": 1,
    "not_provided|RXRB-related_disorder": 2,
    "RXRB-related_disorder": 7,
    "Agammaglobulinemia_9|_autosomal_recessive|not_provided": 3,
    "Agammaglobulinemia_9|_autosomal_recessive": 5,
    "SLC39A7-related_disorder|not_provided": 1,
    "not_provided|Agammaglobulinemia_9|_autosomal_recessive": 1,
    "MHC_class_I_deficiency_3": 1,
    "MHC_class_I_deficiency|TAPBP-related_disorder": 3,
    "TAPBP-related_disorder|MHC_class_I_deficiency": 3,
    "MHC_class_I_deficiency_1|not_specified|MHC_class_I_deficiency": 1,
    "not_provided|not_specified|MHC_class_I_deficiency": 1,
    "TAPBP-related_disorder": 2,
    "not_provided|TAPBP-related_disorder|MHC_class_I_deficiency": 1,
    "MHC_class_I_deficiency|TAPBP-related_disorder|not_provided": 1,
    "not_provided|MHC_class_I_deficiency|TAPBP-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5": 31,
    "Intellectual_disability|_autosomal_dominant_5": 1043,
    "Intellectual_disability|_autosomal_dominant_5|not_provided": 66,
    "Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Intellectual_disability|_autosomal_dominant_5": 67,
    "SYNGAP1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_5": 3,
    "Intellectual_disability|_autosomal_dominant_5|not_provided|Inborn_genetic_diseases": 6,
    "not_provided|Intellectual_disability|Intellectual_disability|_autosomal_dominant_5": 2,
    "not_specified|Intellectual_disability|_autosomal_dominant_5": 9,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_5": 11,
    "Intellectual_disability|_autosomal_dominant_5|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "SYNGAP1-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_5": 3,
    "SYNGAP1-related_disorder|Intellectual_disability|_autosomal_dominant_5|not_provided": 3,
    "Infantile_epilepsy_syndrome|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5|not_provided": 4,
    "Inborn_genetic_diseases|SYNGAP1-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_5|not_provided|Intellectual_disability|_autosomal_dominant_5|Intellectual_disability": 1,
    "SYNGAP1-related_disorder": 11,
    "Complex_neurodevelopmental_disorder|not_provided|Intellectual_disability|_autosomal_dominant_5": 3,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5|not_provided": 1,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_5": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_5": 3,
    "SYNGAP1-related_disorder|not_provided": 1,
    "SYNGAP1-related_disorder|Intellectual_disability|_autosomal_dominant_5": 11,
    "Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 32,
    "Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_5": 1,
    "Intellectual_disability|_autosomal_dominant_5|SYNGAP1-related_disorder|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Seizure": 1,
    "Intellectual_disability|_autosomal_dominant_5|not_provided|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Global_developmental_delay|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|SYNGAP1-related_disorder": 1,
    "SYNGAP1-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_5": 2,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_5": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_5": 2,
    "SYNGAP1-related_encephalopathy|Intellectual_disability|_autosomal_dominant_5": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_dominant_5": 2,
    "not_provided|Complex_neurodevelopmental_disorder|Autosomal_dominant_epilepsy|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Atypical_behavior|Motor_delay|Delayed_speech_and_language_development": 1,
    "Intellectual_disability|_autosomal_dominant_5|Intellectual_disability|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_5|SYNGAP1-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5": 2,
    "SYNGAP1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Intellectual_disability|_autosomal_dominant_5": 1,
    "SYNGAP1-related_disorder|not_specified|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases|not_provided": 1,
    "SYNGAP1-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 2,
    "Complex_neurodevelopmental_disorder|Seizure|Intellectual_disability|_autosomal_dominant_5|Neurodevelopmental_delay|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5|not_specified|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Hereditary_ataxia": 1,
    "not_provided|SYNGAP1-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5": 1,
    "Intellectual_disability|_autosomal_dominant_5|Ptosis|Bulbous_tips_of_toes|Pointed_chin|Atypical_behavior|Aggressive_behavior|High_forehead|Abnormal_sternum_morphology|Delayed_speech_and_language_development|Downslanted_palpebral_fissures|Triangular_face|Wide_nasal_bridge|Motor_delay|Floppy_infant|See_cases|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5|See_cases": 1,
    "Intellectual_disability|_autosomal_dominant_5|Global_developmental_delay|Generalized_hypotonia|Preauricular_skin_tag|Stereotypic_movement_disorder|Delayed_speech_and_language_development": 1,
    "Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_5|not_specified": 6,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_5": 1,
    "SYNGAP1-related_disorder|Intellectual_disability|_autosomal_dominant_5|Complex_neurodevelopmental_disorder|not_provided": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_5|not_provided": 2,
    "Inborn_genetic_diseases|SYNGAP1-related_disorder|Intellectual_disability|_autosomal_dominant_5|not_specified": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_5|Intellectual_disability": 1,
    "Developmental_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|SYNGAP1-related_disorder|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 1,
    "SYNGAP1-related_disorder|Intellectual_disability|_autosomal_dominant_5|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_5|Inborn_genetic_diseases": 1,
    "Cerebellar_ataxia|Global_developmental_delay|Absent_speech|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_5|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|Microcephaly|Epileptic_encephalopathy": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Complex_neurodevelopmental_disorder|Infantile_epileptic_dyskinetic_encephalopathy": 1,
    "SYNGAP1-related_disorder|not_provided|Intellectual_disability|Intellectual_disability|_autosomal_dominant_5": 1,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_5": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|not_specified": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_5|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_5|Complex_neurodevelopmental_disorder": 1,
    "ITPR3-related_disorder": 35,
    "not_provided|ITPR3-related_disorder": 29,
    "not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_type_1J": 1,
    "IMMUNODEFICIENCY_133_WITH_ECTODERMAL_DYSPLASIA_WITH_OR_WITHOUT_PERIPHERAL_NEUROPATHY": 2,
    "ITPR3-related_disorder|not_provided": 20,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1J": 10,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1J|not_specified": 2,
    "not_specified|Charcot-Marie-Tooth_disease|_demyelinating|_type_1J": 2,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1J|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1J|not_provided": 1,
    "not_provided|IMMUNODEFICIENCY_133_WITH_ECTODERMAL_DYSPLASIA_WITH_OR_WITHOUT_PERIPHERAL_NEUROPATHY|ITPR3-related_disorder": 1,
    "not_provided|Diabetes_mellitus_type_1|Charcot-Marie-Tooth_disease|_demyelinating|_type_1J": 1,
    "not_provided|IMMUNODEFICIENCY_133_WITH_ECTODERMAL_DYSPLASIA_WITH_OR_WITHOUT_PERIPHERAL_NEUROPATHY|ITPR3-related_disorder|Charcot-Marie-Tooth_disease|_demyelinating|_type_1J": 1,
    "not_provided|IMMUNODEFICIENCY_133_WITH_ECTODERMAL_DYSPLASIA_WITH_OR_WITHOUT_PERIPHERAL_NEUROPATHY": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_7": 10,
    "Mitochondrial_complex_III_deficiency_nuclear_type_7|not_provided": 5,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_7": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_7|not_specified": 1,
    "UQCC2-related_disorder": 1,
    "Marbach-Rustad_progeroid_syndrome|not_provided|Lipoatrophy|Intention_tremor|Teeth|_supernumerary|Thin_skin|Prominent_superficial_veins|Narrow_mouth|Microcephaly|Proptosis|Dental_crowding|Reduced_bone_mineral_density|Deviated_nasal_septum|Short_stature|Micrognathia|Progeroid_facial_appearance|Multiple_unerupted_teeth|Short_clavicles|Triangular_face|Growth_delay|Abnormal_nasal_dorsum_morphology": 1,
    "not_specified|Cataract_46_juvenile-onset": 1,
    "LEMD2-related_disorder": 3,
    "LEMD2-related_disorder|not_provided": 3,
    "not_provided|LEMD2-related_disorder": 3,
    "Cataract_46_juvenile-onset": 1,
    "Diabetes_mellitus_type_2|_susceptibility_to|not_provided": 1,
    "Diamond-Blackfan_anemia_9": 25,
    "not_provided|Diamond-Blackfan_anemia_9|Diamond-Blackfan_anemia": 2,
    "Diamond-Blackfan_anemia_9|Diamond-Blackfan_anemia": 4,
    "not_specified|Diamond-Blackfan_anemia_9|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_9": 3,
    "RPS10-NUDT3-related_disorder|RPS10-related_disorder|not_provided|Diamond-Blackfan_anemia|not_specified|Diamond-Blackfan_anemia_9": 1,
    "Diamond-Blackfan_anemia|RPS10-related_disorder": 1,
    "not_specified|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_9": 3,
    "RPS10-related_disorder": 2,
    "RPS10-related_disorder|Diamond-Blackfan_anemia": 2,
    "Diamond-Blackfan_anemia_9|Diamond-Blackfan_anemia|RPS10-related_disorder": 1,
    "Diamond-Blackfan_anemia_9|not_specified": 1,
    "not_specified|RPS10-related_disorder|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_9": 1,
    "not_specified|Diamond-Blackfan_anemia_9": 2,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_9|not_specified": 2,
    "RPS10-related_disorder|Diamond-Blackfan_anemia|not_specified|Diamond-Blackfan_anemia_9": 1,
    "Diamond-Blackfan_anemia|RPS10-related_disorder|Diamond-Blackfan_anemia_9|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_9": 1,
    "not_provided|Diamond-Blackfan_anemia_9": 1,
    "not_provided|not_specified|Diamond-Blackfan_anemia_9": 1,
    "Abnormality_of_the_dentition|Abnormal_facial_shape|Short_stature|Abnormality_of_the_skeletal_system|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_2": 4,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_2": 9,
    "Abnormality_of_the_dentition|Abnormal_facial_shape|Short_stature|Abnormality_of_the_skeletal_system": 3,
    "Inborn_genetic_diseases|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_2": 1,
    "Abnormality_of_the_dentition|Abnormal_facial_shape|Short_stature|Abnormality_of_the_skeletal_system|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_2|not_provided": 1,
    "Immunodeficiency_87_and_autoimmunity": 3,
    "not_specified|Immunodeficiency_87_and_autoimmunity": 1,
    "DEF6-related_disorder": 1,
    "not_provided|not_specified|DEF6-related_disorder": 1,
    "DEF6-related_disorder|not_provided": 1,
    "not_provided|Immunodeficiency_87_and_autoimmunity": 2,
    "Fanconi_anemia_complementation_group_E": 603,
    "Fanconi_anemia_complementation_group_E|not_provided": 16,
    "FANCE-related_disorder": 2,
    "Fanconi_anemia_complementation_group_E|Fanconi_anemia": 3,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_E": 6,
    "Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases": 8,
    "FANCE-related_disorder|Fanconi_anemia_complementation_group_E": 4,
    "not_provided|Fanconi_anemia_complementation_group_E": 7,
    "Fanconi_anemia_complementation_group_E|not_specified|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_E|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_E": 15,
    "Fanconi_anemia_complementation_group_E|not_provided|Ovarian_cancer": 1,
    "not_provided|Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_E|FANCE-related_disorder": 1,
    "Fanconi_anemia_complementation_group_E|FANCE-related_disorder": 4,
    "Fanconi_anemia_complementation_group_E|not_provided|Fanconi_anemia|not_specified": 1,
    "not_provided|Fanconi_anemia_complementation_group_E|not_specified": 3,
    "not_provided|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_E": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_E": 3,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_E": 2,
    "FANCE-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_E|not_provided": 1,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_E": 1,
    "not_provided|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_E|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_E": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_E": 1,
    "Fanconi_anemia_complementation_group_E|Ovarian_cancer": 1,
    "not_specified|Fanconi_anemia_complementation_group_E": 4,
    "Fanconi_anemia_complementation_group_E|not_specified": 7,
    "Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCE-related_disorder|Fanconi_anemia_complementation_group_E": 1,
    "not_specified|Fanconi_anemia_complementation_group_E|Carcinoma_of_colon": 1,
    "Fanconi_anemia_complementation_group_E|not_specified|not_provided": 3,
    "FANCE-related_disorder|Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_E|Fanconi_anemia|not_provided": 2,
    "FANCE-related_disorder|not_specified|Fanconi_anemia_complementation_group_E|Fanconi_anemia": 1,
    "FANCE-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_E": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases|not_provided": 2,
    "Fanconi_anemia_complementation_group_E|not_provided|not_specified": 1,
    "not_provided|Carcinoma_of_pancreas|Fanconi_anemia_complementation_group_E": 1,
    "Exstrophy-epispadias_complex|Ovarian_cancer|not_specified|Fanconi_anemia_complementation_group_E": 1,
    "not_provided|Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_E|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_E|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_E|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|not_provided|FANCE-related_disorder|Fanconi_anemia_complementation_group_E": 1,
    "FANCE-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_E": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_E|FANCE-related_disorder": 1,
    "not_specified|Fanconi_anemia_complementation_group_E|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_E|not_specified|FANCE-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_E|Ovarian_cancer|not_specified": 1,
    "Fanconi_anemia_complementation_group_E|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_E": 1,
    "Fanconi_anemia_complementation_group_E|FANCE-related_disorder|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_E|not_specified": 1,
    "Leber_congenital_amaurosis_15|Retinitis_pigmentosa": 8,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_15": 2,
    "Leber_congenital_amaurosis_15|not_provided": 3,
    "Retinitis_pigmentosa_14": 13,
    "Leber_congenital_amaurosis_15|Retinitis_pigmentosa_14": 7,
    "Leber_congenital_amaurosis_15": 13,
    "not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa": 4,
    "Leber_congenital_amaurosis_15|not_provided|Retinitis_pigmentosa": 6,
    "not_provided|Leber_congenital_amaurosis_15": 2,
    "Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided": 2,
    "not_provided|not_specified|Leber_congenital_amaurosis_15": 1,
    "not_provided|Retinitis_pigmentosa_14": 4,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "not_provided|Leber_congenital_amaurosis|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis_15|Retinitis_pigmentosa|not_provided": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "TULP1-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_15": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa_14": 1,
    "Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa_14": 4,
    "Leber_congenital_amaurosis|not_provided|Retinitis_pigmentosa_14": 1,
    "not_provided|TULP1-related_disorder|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis_1|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|TULP1-related_disorder|not_provided|not_specified": 1,
    "Retinitis_pigmentosa_14|Leber_congenital_amaurosis|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|TULP1-related_disorder|not_provided": 1,
    "TULP1-related_disorder": 2,
    "Leber_congenital_amaurosis_15|Retinitis_pigmentosa_14|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided|Leber_congenital_amaurosis|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15": 2,
    "not_provided|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|Leber_congenital_amaurosis|not_provided": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Leber_congenital_amaurosis_15|not_provided|Retinal_degeneration|Polydactyly|_postaxial|_type_A1|Syndactyly|Brachydactyly": 1,
    "Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Leber_congenital_amaurosis|Retinitis_pigmentosa_14|not_provided": 1,
    "Retinitis_pigmentosa_14|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_15|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_14": 1,
    "Retinitis_pigmentosa_14|not_provided|Leber_congenital_amaurosis": 1,
    "not_specified|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_1": 1,
    "Retinitis_pigmentosa_14|not_provided": 1,
    "not_provided|TULP1-related_disorder|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided": 1,
    "Leber_congenital_amaurosis_15|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|TULP1-related_disorder": 2,
    "Leber_congenital_amaurosis_1|Retinitis_pigmentosa_14|Leber_congenital_amaurosis|Leber_congenital_amaurosis_15|not_provided": 1,
    "Leber_congenital_amaurosis_15|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_15|Autosomal_recessive_retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa_14|Abnormality_of_the_eye": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_15|not_provided": 2,
    "Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_15": 1,
    "Leber_congenital_amaurosis_15|not_provided|Retinitis_pigmentosa|TULP1-related_disorder": 1,
    "Retinitis_pigmentosa|not_specified|not_provided|Leber_congenital_amaurosis_15": 1,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_15": 1,
    "Leber_congenital_amaurosis_15|not_provided|Retinitis_pigmentosa_14": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_15|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa|Leber_congenital_amaurosis_1|Retinitis_pigmentosa_14": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_1": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_14": 1,
    "Inborn_genetic_diseases|not_provided|TULP1-related_disorder": 1,
    "Leber_congenital_amaurosis_15|Retinitis_pigmentosa_14|not_provided": 1,
    "TULP1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Leber_congenital_amaurosis_15": 1,
    "TULP1-related_disorder|Retinitis_pigmentosa|Leber_congenital_amaurosis_15|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_15|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_15|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TULP1-related_disorder": 1,
    "TULP1-related_disorder|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Leber_congenital_amaurosis_15|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_15|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_14|Leber_congenital_amaurosis_15|Retinitis_pigmentosa|not_specified|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_15|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "See_cases|Retinitis_pigmentosa_14": 1,
    "Susceptibility_to_severe_depressive_disorder": 6,
    "Asthma": 1,
    ".|Antidepressant_drug_treatment|_accelerated_response_to": 1,
    "Post-traumatic_stress_disorder": 2,
    "Spermatogenic_failure_90": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_67": 70,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_67": 5,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_67": 1,
    "LHFPL5-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_67|Hearing_loss|_autosomal_recessive": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_67|LHFPL5-related_disorder": 1,
    "LHFPL5-related_disorder|not_provided": 2,
    "LHFPL5-related_disorder|not_provided|not_specified": 2,
    "not_specified|Deafness|not_provided": 1,
    "LHFPL5-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_67|not_provided|LHFPL5-related_disorder": 1,
    "Autosomal_recessive_non-syndromic_intellectual_disability|Autosomal_recessive_nonsyndromic_hearing_loss_67": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_67|Ear_malformation": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_67|not_provided": 4,
    "not_provided|SLC26A8-related_disorder": 2,
    "Spermatogenic_failure_3": 9,
    "SLC26A8-related_disorder": 6,
    "not_provided|Spermatogenic_failure_3|not_specified": 1,
    "SLC26A8-related_disorder|not_provided": 1,
    "Autism|Delayed_speech_and_language_development|Colitis|Cranial_asymmetry": 1,
    "Autosomal_recessive_congenital_ichthyosis_10": 55,
    "Autosomal_recessive_congenital_ichthyosis_10|PNPLA1-related_disorder|not_provided": 2,
    "Congenital_ichthyosiform_erythroderma|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "Congenital_ichthyosiform_erythroderma|not_provided|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_10": 2,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_10": 11,
    "Autosomal_recessive_congenital_ichthyosis_10|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_10": 4,
    "Autosomal_recessive_congenital_ichthyosis_10|Lamellar_ichthyosis": 2,
    "PNPLA1-related_disorder": 2,
    "Autosomal_recessive_congenital_ichthyosis_10|Congenital_ichthyosiform_erythroderma": 2,
    "Autosomal_recessive_congenital_ichthyosis_10|not_specified": 2,
    "PNPLA1-related_disorder|Autosomal_recessive_congenital_ichthyosis_10|not_provided": 1,
    "not_provided|Ichthyosis|Autosomal_recessive_congenital_ichthyosis_10|Autosomal_recessive_congenital_ichthyosis": 1,
    "Congenital_ichthyosiform_erythroderma|Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_10|not_specified": 2,
    "Lamellar_ichthyosis|Congenital_ichthyosiform_erythroderma|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "PNPLA1-related_disorder|not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "Congenital_ichthyosiform_erythroderma|not_provided|Lamellar_ichthyosis": 1,
    "Autosomal_recessive_congenital_ichthyosis_10|not_provided": 3,
    "Autosomal_recessive_congenital_ichthyosis_10|not_provided|Lamellar_ichthyosis|Congenital_ichthyosiform_erythroderma": 1,
    "not_provided|Congenital_ichthyosiform_erythroderma": 2,
    "Autosomal_recessive_congenital_ichthyosis_10|not_provided|PNPLA1-related_disorder": 1,
    "Autosomal_recessive_congenital_ichthyosis_10|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_recessive_congenital_ichthyosis_10|not_provided|not_specified": 1,
    "PNPLA1-related_disorder|not_provided|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "Autosomal_recessive_congenital_ichthyosis_10|Congenital_ichthyosiform_erythroderma|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_10|not_specified|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_10": 2,
    "CIP1/WAF1_TUMOR-ASSOCIATED_POLYMORPHISM_1": 1,
    "Congenital_pontocerebellar_hypoplasia": 5,
    "Congenital_pontocerebellar_hypoplasia|Pontocerebellar_hypoplasia|_type_14|not_provided|not_specified": 1,
    "Pontocerebellar_hypoplasia|_type_14": 7,
    "Congenital_pontocerebellar_hypoplasia|Pontocerebellar_hypoplasia|_type_14": 2,
    "Pontocerebellar_hypoplasia|_type_14|not_provided|Congenital_pontocerebellar_hypoplasia": 1,
    "Neurodevelopmental_disorder|Congenital_pontocerebellar_hypoplasia|Pontocerebellar_hypoplasia|_type_14": 1,
    "Autism|_susceptibility_to|_1": 1,
    "DNAH8-related_disorder": 10,
    "Spermatogenic_failure_46|Primary_ciliary_dyskinesia": 8,
    "Primary_ciliary_dyskinesia|DNAH8-related_disorder|not_specified": 1,
    "Spermatogenic_failure_46": 10,
    "Primary_ciliary_dyskinesia|Spermatogenic_failure_46|not_specified": 3,
    "Primary_ciliary_dyskinesia|Spermatogenic_failure_46|not_provided": 2,
    "not_specified|Primary_ciliary_dyskinesia|DNAH8-related_disorder": 2,
    "DNAH8-related_disorder|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|DNAH8-related_disorder": 17,
    "not_specified|Spermatogenic_failure_46": 2,
    "DNAH8-related_disorder|Primary_ciliary_dyskinesia": 14,
    "Primary_ciliary_dyskinesia|DNAH8-related_disorder|not_provided": 4,
    "DNAH8-related_disorder|Primary_ciliary_dyskinesia|not_specified|not_provided": 2,
    "Spermatogenic_failure_46|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_provided|DNAH8-related_disorder|Spermatogenic_failure_46|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Spermatogenic_failure_46": 9,
    "not_provided|Primary_ciliary_dyskinesia|Spermatogenic_failure_46": 2,
    "DNAH8-related_disorder|Primary_ciliary_dyskinesia|not_provided|not_specified": 1,
    "not_provided|DNAH8-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_specified|Spermatogenic_failure_46": 2,
    "Spermatogenic_failure_46|not_specified|Primary_ciliary_dyskinesia|not_provided": 1,
    "Spermatogenic_failure_46|not_provided|Primary_ciliary_dyskinesia": 4,
    "DNAH8-related_disorder|Spermatogenic_failure_46|Primary_ciliary_dyskinesia": 1,
    "not_specified|DNAH8-related_disorder|Primary_ciliary_dyskinesia": 1,
    "DNAH8-related_disorder|not_provided|Primary_ciliary_dyskinesia": 3,
    "Inherited_obesity|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|DNAH8-related_disorder|not_specified": 1,
    "not_provided|DNAH8-related_disorder|not_specified|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia|DNAH8-related_disorder|not_specified|not_provided": 1,
    "DNAH8-related_disorder|Primary_ciliary_dyskinesia|not_specified": 1,
    "Spermatogenic_failure_46|not_specified|Primary_ciliary_dyskinesia": 4,
    "not_provided|Primary_ciliary_dyskinesia|DNAH8-related_disorder": 2,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Spermatogenic_failure_46": 1,
    "Recurrent_infections_of_the_middle_ear|Recurrent_respiratory_infections|Recurrent_infections": 1,
    "Primary_ciliary_dyskinesia|not_specified|DNAH8-related_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia|Spermatogenic_failure_46|not_specified": 1,
    "Spermatogenic_failure_46|not_specified": 1,
    "KCNK5-related_disorder": 2,
    "KIF6-related_disorder": 2,
    "pravastatin_response_-_Efficacy": 1,
    "DAAM2-related_disorder": 44,
    "Inborn_genetic_diseases|DAAM2-related_disorder": 2,
    "not_provided|DAAM2-related_disorder": 2,
    "DAAM2-related_disorder|not_provided": 3,
    "Nephrotic_syndrome|_type_24": 7,
    "DAAM2-related_disorder|Nephrotic_syndrome|_type_24|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_24": 2,
    "Nephrotic_syndrome|_type_24|Idiopathic_multidrug-resistant_nephrotic_syndrome|DAAM2-related_disorder": 1,
    "DAAM2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|DAAM2-related_disorder|not_provided": 1,
    "DAAM2-related_disorder|not_provided|Nephrotic_syndrome|_type_24": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 607,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 20,
    "Combined_molybdoflavoprotein_enzyme_deficiency": 15,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|not_provided": 17,
    "MOCS1-related_disorder": 5,
    "MOCS1-related_disorder|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 2,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_B": 1,
    "not_provided|Combined_molybdoflavoprotein_enzyme_deficiency|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "MOCS1-related_disorder|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 6,
    "Combined_molybdoflavoprotein_enzyme_deficiency|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Inborn_genetic_diseases": 20,
    "Inborn_genetic_diseases|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 18,
    "MOCS1-related_disorder|not_specified|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|MOCS1-related_disorder|Intellectual_disability|Inborn_genetic_diseases|not_specified": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|MOCS1-related_disorder": 4,
    "Intellectual_disability|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|MOCS1-related_disorder|Inborn_genetic_diseases|Intellectual_disability|not_specified|not_provided": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|MOCS1-related_disorder|not_provided|not_specified": 1,
    "not_specified|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|not_provided|MOCS1-related_disorder": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|not_provided|Inborn_genetic_diseases": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Intellectual_disability|MOCS1-related_disorder|Inborn_genetic_diseases|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Inborn_genetic_diseases|not_specified": 1,
    "Intellectual_disability|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Inborn_genetic_diseases": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|MOCS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "MOCS1-related_disorder|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|not_provided": 2,
    "MOCS1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "not_provided|not_specified|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_provided|MOCS1-related_disorder|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A": 1,
    "TREM2-related_disorder": 2,
    "not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2": 4,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|not_provided": 9,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 15,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|not_provided|not_specified": 1,
    "TREM2-related_disorder|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|not_provided": 2,
    "TREM2-related_disorder|not_provided": 5,
    "not_provided|TREM2-related_disorder": 4,
    "TREM2-related_disorder|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2": 2,
    "not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1|not_specified": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2": 9,
    "not_provided|Inborn_genetic_diseases|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1|TREM2-related_disorder": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 3,
    "not_specified|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2": 1,
    "not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|Inborn_genetic_diseases": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|TREM2-related_disorder|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|TREM2-related_disorder|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 8,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|TREM2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 3,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|not_specified|not_provided": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "TREM2-related_disorder|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|not_specified|not_provided": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|Frontotemporal_dementia|not_provided": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_2|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephaly|Inborn_genetic_diseases|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "FOXP4-related_disorder": 1,
    "Ventricular_septal_defect|Laryngeal_hypoplasia|Global_developmental_delay|Feeding_difficulties|not_provided": 1,
    "FOXP4-related_neurodevelopmental_disorder": 1,
    "not_specified|FOXP4-related_disorder": 1,
    "Developmental_Disorder_With_Language_Delay_And_Congenital_Abnormalities": 1,
    "not_provided|Sensorineural_hearing_loss_disorder|Ventricular_septal_defect|Short_stature|Hearing_impairment|Epiphyseal_dysplasia|Flattened_epiphysis|Disproportionate_short_stature|Craniofacial_asymmetry": 1,
    "not_specified|Neurodevelopmental_disorder_with_severe_motor_impairment|_absent_language|_cerebral_hypomyelination|_and_brain_atrophy": 2,
    "Neurodevelopmental_disorder_with_severe_motor_impairment|_absent_language|_cerebral_hypomyelination|_and_brain_atrophy": 6,
    "TAF8-related_disorder|Neurodevelopmental_disorder_with_severe_motor_impairment|_absent_language|_cerebral_hypomyelination|_and_brain_atrophy|Partial_agenesis_of_the_corpus_callosum|Severe_global_developmental_delay|Microcephaly": 1,
    "Cone_dystrophy_3": 42,
    "not_provided|Cone_dystrophy_3": 9,
    "not_provided|Cone_dystrophy_3|not_specified": 1,
    "not_provided|GUCA1A-related_disorder": 2,
    "Cone_dystrophy_3|not_provided": 6,
    "not_provided|Usher_syndrome|Cone_dystrophy_3|Macular_dystrophy": 1,
    "Rod-cone_dystrophy|not_provided": 2,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_14|Cone_dystrophy_3": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Macular_dystrophy|Cone_dystrophy_3": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy|Cone_dystrophy_3": 1,
    "Cone_dystrophy_3|not_provided|Retinal_dystrophy": 1,
    "not_provided|Isolated_macular_dystrophy|Cone_dystrophy_3": 1,
    "Inborn_genetic_diseases|not_provided|Cone_dystrophy_3": 1,
    "Retinal_dystrophy|See_cases": 1,
    "Retinitis_pigmentosa|Cone_dystrophy_3": 1,
    "Cone-rod_dystrophy_14|Retinal_dystrophy|not_provided": 1,
    "Cone_dystrophy_3|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Cone_dystrophy_3": 1,
    "Cone_dystrophy_3|not_provided|Cone_dystrophy|not_specified|Retinitis_Pigmentosa|_Dominant": 1,
    "not_provided|Inborn_genetic_diseases|Cone_dystrophy_3": 2,
    "not_specified|GUCA1A-related_disorder|not_provided": 1,
    "Cone_dystrophy_3|Retinitis_Pigmentosa|_Dominant": 2,
    "Cone_dystrophy|Retinitis_Pigmentosa|_Dominant|not_provided|Cone_dystrophy_3": 1,
    "Cone_dystrophy|Retinitis_Pigmentosa|_Dominant|Cone_dystrophy_3": 3,
    "Cone_dystrophy|Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa": 11,
    "Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa|Cone_dystrophy": 1,
    "Cone_dystrophy|Retinitis_Pigmentosa|_Dominant|not_provided|Retinitis_pigmentosa": 3,
    "not_provided|Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa|Cone_dystrophy": 1,
    "not_provided|Cone_dystrophy|Retinitis_Pigmentosa|_Dominant|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_48": 1,
    "Retinitis_pigmentosa_48|not_provided": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_48": 1,
    "Retinitis_pigmentosa_48|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_48": 1,
    "Retinitis_pigmentosa_48": 1,
    "Retinitis_pigmentosa_48|not_specified": 1,
    "Pigmentary_retinal_dystrophy|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy|Pigmentary_retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 4,
    "Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 12,
    "not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy|Pigmentary_retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 3,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 6,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy|Pigmentary_retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Choroidal_dystrophy|_central_areolar_2|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 2,
    "not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Adult-onset_foveomacular_vitelliform_dystrophy|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 3,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Adult-onset_foveomacular_vitelliform_dystrophy|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 2,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Adult-onset_foveomacular_vitelliform_dystrophy|not_provided|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 4,
    "Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy|Patterned_macular_dystrophy_1": 1,
    "not_provided|Retinitis_Pigmentosa|_Dominant|Patterned_macular_dystrophy_1|Vitelliform_macular_dystrophy|Choroidal_Dystrophy|Cone-Rod_Dystrophy|_Dominant|Pigmentary_retinal_dystrophy": 2,
    "Retinitis_Pigmentosa|_Dominant|Patterned_macular_dystrophy_1|Vitelliform_macular_dystrophy|Choroidal_Dystrophy|Cone-Rod_Dystrophy|_Dominant|Pigmentary_retinal_dystrophy": 1,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Adult-onset_foveomacular_vitelliform_dystrophy|not_provided|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 2,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Adult-onset_foveomacular_vitelliform_dystrophy|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 4,
    "not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Adult-onset_foveomacular_vitelliform_dystrophy|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 1,
    "Vitelliform_macular_dystrophy_3|not_specified|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder": 283,
    "PRPH2-related_disorder|not_provided|Retinal_dystrophy": 4,
    "not_provided|PRPH2-related_disorder|Retinal_dystrophy": 5,
    "not_provided|PRPH2-related_disorder": 41,
    "Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Patterned_macular_dystrophy_1|Retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy|PRPH2-related_disorder|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy|PRPH2-related_disorder|Macular_dystrophy": 1,
    "Retinal_dystrophy|PRPH2-related_disorder": 7,
    "PRPH2-related_disorder|Retinal_dystrophy": 11,
    "Retinitis_pigmentosa|PRPH2-related_disorder|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|not_provided": 19,
    "not_provided|Vitelliform_macular_dystrophy_3": 2,
    "Multifocal_pattern_dystrophy_simulating_fundus_flavimaculatus|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|PRPH2-related_disorder|Retinitis_pigmentosa": 1,
    "PRPH2-related_disorder|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|Stargardt_disease|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "not_provided|PRPH2-related_disorder|Vitelliform_macular_dystrophy_3|Retinal_dystrophy": 1,
    "Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_7|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|Vitelliform_macular_dystrophy_3|not_provided": 1,
    "Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Patterned_macular_dystrophy_1|Vitelliform_macular_dystrophy_3|Pigmentary_retinal_dystrophy": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_7": 2,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium": 1,
    "not_provided|Pigmentary_retinal_dystrophy|Vitelliform_macular_dystrophy_3|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Patterned_macular_dystrophy_1|PRPH2-related_disorder": 1,
    "not_provided|Choroidal_dystrophy|_central_areolar_2|PRPH2-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa_7": 3,
    "Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Retinal_dystrophy|not_specified|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|Retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy|PRPH2-related_disorder|Cone-rod_dystrophy": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|PRPH2-related_disorder|not_provided|Retinal_dystrophy|Vitelliform_macular_dystrophy_2": 1,
    "not_provided|Retinal_dystrophy|Vitelliform_macular_dystrophy_2|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|not_provided|Patterned_macular_dystrophy_1|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|PRPH2-related_disorder|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Retinitis_pigmentosa|PRPH2-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_7|Pigmentary_retinal_dystrophy|Vitelliform_macular_dystrophy_3|Choroidal_dystrophy|_central_areolar_2|Patterned_macular_dystrophy_1|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Patterned_macular_dystrophy_1": 7,
    "Choroidal_dystrophy|_central_areolar_2": 2,
    "Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|PRPH2-related_disorder|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Patterned_macular_dystrophy_1|not_provided": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroideremia|Stargardt_disease|Doyne_honeycomb_retinal_dystrophy|Cone-rod_dystrophy|Vitelliform_macular_dystrophy_2": 1,
    "Vitelliform_macular_dystrophy_3|not_provided": 1,
    "PRPH2-related_disorder|Stargardt_disease|not_provided": 5,
    "PRPH2-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|Vitelliform_macular_dystrophy_2": 1,
    "not_provided|Macular_dystrophy|PRPH2-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_7": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided": 11,
    "not_specified|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|Adult-onset_foveomacular_vitelliform_dystrophy|Pigmentary_retinal_dystrophy": 1,
    "Pigmentary_retinal_dystrophy": 31,
    "Patterned_macular_dystrophy_1|not_provided": 2,
    "Patterned_macular_dystrophy_1|Vitelliform_macular_dystrophy_3": 1,
    "PRPH2-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|PRPH2-related_disorder|Retinitis_pigmentosa|Patterned_dystrophy_of_the_retinal_pigment_epithelium": 1,
    "Patterned_macular_dystrophy_1|not_provided|Retinal_dystrophy": 1,
    "Stargardt_disease|not_provided|PRPH2-related_disorder": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_7": 1,
    "PRPH2-related_disorder|not_provided|Retinitis_pigmentosa_7": 1,
    "PRPH2-related_disorder|Cone-rod_dystrophy|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|Vitelliform_macular_dystrophy_3|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_7|Retinal_dystrophy": 1,
    "PRPH2-related_disorder|Stargardt_disease|not_provided|Usher_syndrome": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|Macular_dystrophy|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Choroidal_dystrophy|_central_areolar_2|Stargardt_disease": 1,
    "PRPH2-related_disorder|not_specified|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|Stargardt_disease|PRPH2-related_disorder|not_provided|Retinal_dystrophy": 1,
    "PRPH2-related_disorder|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_7|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy": 1,
    "Stargardt_disease|Patterned_dystrophy_of_the_retinal_pigment_epithelium|not_provided|PRPH2-related_disorder": 1,
    "Adult-onset_foveomacular_vitelliform_dystrophy": 2,
    "not_provided|Retinal_dystrophy|Stargardt_disease|PRPH2-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|Retinitis_pigmentosa|Patterned_dystrophy_of_the_retinal_pigment_epithelium|not_provided|Retinal_dystrophy": 1,
    "PRPH2-related_disorder|Macular_dystrophy|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_7|not_provided": 2,
    "PRPH2-related_disorder|not_provided|Vitelliform_macular_dystrophy_3|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Macular_dystrophy|Retinal_dystrophy": 1,
    "Retinal_dystrophy|PRPH2-related_disorder|not_provided": 2,
    "Isolated_macular_dystrophy|not_provided|PRPH2-related_disorder|Stargardt_disease": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|PRPH2-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|PRPH2-related_disorder": 1,
    "not_provided|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Retinitis_Pigmentosa|_Dominant|Patterned_macular_dystrophy_1|PRPH2-related_disorder|Vitelliform_macular_dystrophy|Choroidal_Dystrophy|Cone-Rod_Dystrophy|_Dominant|Pigmentary_retinal_dystrophy": 1,
    "PRPH2-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Retinitis_pigmentosa_7": 1,
    "Retinal_dystrophy|not_provided|PRPH2-related_disorder": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|PRPH2-related_disorder": 1,
    "Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Vitelliform_macular_dystrophy_3|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy": 1,
    "not_provided|Stargardt_disease|PRPH2-related_disorder": 2,
    "PRPH2-related_disorder|Patterned_dystrophy_of_the_retinal_pigment_epithelium|not_provided": 1,
    "Stargardt_disease|PRPH2-related_disorder|not_provided|Retinal_dystrophy|Patterned_macular_dystrophy_1": 1,
    "PRPH2-related_disorder|Leber_congenital_amaurosis_18|not_provided|Patterned_macular_dystrophy_1": 1,
    "Adult-onset_foveomacular_vitelliform_dystrophy|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Vitelliform_macular_dystrophy_2|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "not_provided|PRPH2-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "PRPH2-related_disorder|Retinitis_pigmentosa|not_provided": 3,
    "not_provided|Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Stargardt_disease|Retinal_dystrophy|Vitelliform_macular_dystrophy_2": 1,
    "PRPH2-related_disorder|not_provided|Vitelliform_macular_dystrophy_2": 1,
    "Patterned_macular_dystrophy_1|PRPH2-related_disorder": 1,
    "Pigmentary_retinal_dystrophy|PRPH2-related_disorder|not_provided": 1,
    "not_provided|Macular_dystrophy": 3,
    "Retinitis_pigmentosa_7|not_provided|PRPH2-related_disorder": 1,
    "not_provided|Stargardt_disease|Macular_dystrophy|PRPH2-related_disorder|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|Retinal_dystrophy|Patterned_macular_dystrophy_1": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Vitelliform_macular_dystrophy_2": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|Stargardt_disease|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Vitelliform_macular_dystrophy_2": 1,
    "not_provided|PRPH2-related_disorder|Retinal_dystrophy|Patterned_dystrophy_of_the_retinal_pigment_epithelium": 2,
    "PRPH2-related_disorder|Patterned_macular_dystrophy_1": 2,
    "not_provided|Patterned_dystrophy_of_the_retinal_pigment_epithelium|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Choroidal_dystrophy|_central_areolar_2": 1,
    "PRPH2-related_disorder|not_provided|Patterned_macular_dystrophy_1|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "PRPH2-related_disorder|not_provided|Patterned_macular_dystrophy_1|Retinal_dystrophy|Patterned_dystrophy_of_the_retinal_pigment_epithelium": 1,
    "Vitelliform_macular_dystrophy_2|not_provided": 9,
    "Retinal_dystrophy|PRPH2-related_disorder|not_provided|Choroideremia|Stargardt_disease": 1,
    "Inborn_genetic_diseases|PRPH2-related_disorder": 2,
    "PRPH2-related_disorder|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Leber_congenital_amaurosis_18|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|_digenic": 1,
    "Choroidal_dystrophy|_central_areolar_2|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_7|Pigmentary_retinal_dystrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_7|PRPH2-related_disorder|Retinitis_pigmentosa|not_provided": 1,
    "Choroidal_dystrophy|_central_areolar_2|Retinitis_pigmentosa_7|not_provided|PRPH2-related_disorder": 1,
    "Retinitis_pigmentosa_7|PRPH2-related_disorder|not_provided": 1,
    "PRPH2-related_disorder|Retinitis_pigmentosa|Retinitis_pigmentosa_7|not_provided": 1,
    "Vitelliform_macular_dystrophy_3|Patterned_dystrophy_of_the_retinal_pigment_epithelium|Macular_dystrophy|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Stargardt_disease": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Stargardt_disease|Cone-rod_dystrophy|Vitelliform_macular_dystrophy_2|maculopathy": 1,
    "PRPH2-related_disorder|Vitelliform_macular_dystrophy_3|not_provided": 1,
    "not_provided|Retinal_dystrophy|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|not_provided|Patterned_macular_dystrophy_1": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease": 1,
    "PRPH2-related_disorder|Pigmentary_retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa_7|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Cone-rod_dystrophy|not_provided|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Vitelliform_macular_dystrophy_3": 1,
    "Pigmentary_retinal_dystrophy|PRPH2-related_disorder|not_provided|Retinal_dystrophy|Pigmentary_retinopathy|Macular_degeneration|Abnormality_of_retinal_pigmentation|Blurred_vision|Retinitis_pigmentosa|Stargardt_disease": 1,
    "Multifocal_pattern_dystrophy_simulating_fundus_flavimaculatus": 1,
    "Retinitis_pigmentosa|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Stargardt_disease|Cone-rod_dystrophy": 1,
    "Retinal_dystrophy|PRPH2-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|not_provided|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|PRPH2-related_disorder|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Stargardt_disease|maculopathy": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|Progressive_cone_dystrophy_(without_rod_involvement)|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Stargardt_disease|maculopathy|Cone_dystrophy": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|Vitelliform_macular_dystrophy_3|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|PRPH2-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Stargardt_disease|Cone-rod_dystrophy|Autosomal_recessive_bestrophinopathy": 1,
    "Retinitis_pigmentosa_7|Retinal_dystrophy|PRPH2-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "not_specified|PRPH2-related_disorder": 1,
    "PRPH2-related_disorder|Retinitis_pigmentosa|Stargardt_disease|Retinal_dystrophy|not_provided": 1,
    "PRPH2-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "PRPH2-related_disorder|not_provided|Stargardt_disease|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa|PRPH2-related_disorder|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy|not_provided|Patterned_macular_dystrophy_1": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_7": 2,
    "PRPH2-associated_retinal_disease": 1,
    "Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "not_provided|Isolated_macular_dystrophy|Vitelliform_macular_dystrophy_3|Choroidal_dystrophy|_central_areolar_2|Retinitis_pigmentosa_7|Patterned_macular_dystrophy_1|Retinal_dystrophy": 1,
    "PRPH2-related_disorder|Patterned_dystrophy_of_the_retinal_pigment_epithelium|not_provided|Retinal_dystrophy|Stargardt_disease": 1,
    "not_specified|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy|PRPH2-related_disorder|Retinitis_pigmentosa|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Vitelliform_macular_dystrophy_3|Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "not_provided|Stargardt_disease|PRPH2-related_disorder|Patterned_dystrophy_of_the_retinal_pigment_epithelium": 1,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy|PRPH2-related_disorder|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_specified": 1,
    "Central_areolar_choroidal_dystrophy": 1,
    "Patterned_dystrophy_of_the_retinal_pigment_epithelium|Stargardt_disease|PRPH2-related_disorder|not_provided": 1,
    "Retinal_dystrophy|PRPH2-related_disorder|not_provided|Stargardt_disease": 1,
    "PRPH2-related_disorder|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|not_provided|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_specified|not_provided|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Retinal_dystrophy|Stargardt_disease|PRPH2-related_disorder|not_provided": 1,
    "not_provided|PRPH2-related_disorder|Inborn_genetic_diseases": 1,
    "Pigmentary_retinal_dystrophy|Vitelliform_macular_dystrophy_3|Retinitis_pigmentosa_7|Patterned_macular_dystrophy_1|Choroidal_dystrophy|_central_areolar_2": 1,
    "Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Inborn_genetic_diseases|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Patterned_macular_dystrophy_1|Patterned_dystrophy_of_the_retinal_pigment_epithelium|not_provided|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Retinal_dystrophy|Stargardt_disease": 1,
    "PRPH2-related_disorder|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|not_provided|Retinal_dystrophy|Stargardt_disease": 1,
    "Vitelliform_macular_dystrophy_3|Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|PRPH2-related_disorder|Optic_atrophy|Retinal_dystrophy|not_specified|not_provided|Stargardt_disease": 1,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Adult-onset_foveomacular_vitelliform_dystrophy|PRPH2-related_disorder|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy": 1,
    "not_provided|Retinitis_punctata_albescens|_autosomal_dominant": 1,
    "not_provided|Choroidal_dystrophy|_central_areolar_2|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|PRPH2-related_disorder|Retinal_dystrophy|Cone-rod_dystrophy|Patterned_macular_dystrophy_1|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "PRPH2-related_disorder|Retinal_dystrophy|not_provided|Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa_7|Choroidal_dystrophy|_central_areolar_2|Pigmentary_retinal_dystrophy|Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Inborn_genetic_diseases": 1,
    "Vitelliform_macular_dystrophy_3|PRPH2-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_specified|Patterned_macular_dystrophy_1|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy|Adult-onset_foveomacular_vitelliform_dystrophy": 1,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Adult-onset_foveomacular_vitelliform_dystrophy|not_provided|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy": 1,
    "Patterned_macular_dystrophy_1|Retinitis_pigmentosa|Adult-onset_foveomacular_vitelliform_dystrophy|Pigmentary_retinal_dystrophy|Choroidal_dystrophy|_central_areolar_2|Cone-rod_dystrophy": 1,
    "Choroidal_Dystrophy|Vitelliform_macular_dystrophy|Pigmentary_retinal_dystrophy|Cone-Rod_Dystrophy|_Dominant|Retinitis_Pigmentosa|_Dominant|Patterned_macular_dystrophy_1": 1,
    "PTCRA_POLYMORPHISM": 1,
    "Immunodeficiency_126|_susceptibility_to": 3,
    "CNPY3-related_disorder": 6,
    "Developmental_and_epileptic_encephalopathy|_60": 16,
    "Developmental_and_epileptic_encephalopathy|_60|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_60|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_60": 1,
    "GNMT-related_disorder|not_provided": 1,
    "Glycine_N-methyltransferase_deficiency": 4,
    "not_provided|GNMT-related_disorder": 2,
    "Glycine_N-methyltransferase_deficiency|not_provided": 1,
    "PEX6_POLYMORPHISM|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|not_provided": 1,
    "not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_provided": 3,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 27,
    "not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|not_specified|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|PEX6-related_disorder": 2,
    "PEX6-related_disorder": 17,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder": 7,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 27,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|not_specified|Zellweger_spectrum_disorders|PEX6-related_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder": 46,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 27,
    "PEX6-related_disorder|not_provided|Peroxisome_biogenesis_disorder": 2,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder": 1,
    "Inborn_genetic_diseases|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B": 1,
    "PEX6-related_disorder|Peroxisome_biogenesis_disorder": 18,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 2,
    "Zellweger_spectrum_disorders|not_specified|Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 1,
    "Zellweger_spectrum_disorders|not_specified|Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_2": 38,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 15,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2": 2,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4B": 1,
    "Peroxisome_biogenesis_disorder|Inborn_genetic_diseases": 23,
    "not_provided|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 1,
    "not_specified|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|not_provided": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 11,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|See_cases": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 4,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_specified|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 1,
    "not_specified|Heimler_syndrome_2": 1,
    "Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|Heimler_syndrome_2": 1,
    "not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_provided": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2": 12,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_specified": 1,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_specified|Zellweger_spectrum_disorders": 1,
    "PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|PEX6-related_disorder|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|not_provided": 31,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 13,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B": 1,
    "PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder": 2,
    "Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_specified": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 4,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder|not_specified": 4,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 2,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2": 1,
    "Heimler_syndrome_2|Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder|not_provided": 1,
    "not_provided|Heimler_syndrome_2": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 11,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2|not_specified|not_provided|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 2,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 6,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|Cerebellar_ataxia|Paroxysmal_dystonia|Peripheral_neuropathy|Premature_ovarian_insufficiency|Cognitive_impairment|Sensorineural_hearing_loss_disorder|not_provided": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder": 2,
    "not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_4B": 9,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder": 16,
    "Zellweger_spectrum_disorders|PEX6-related_disorder|Peroxisome_biogenesis_disorder": 2,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|See_cases": 1,
    "Zellweger_spectrum_disorders|PEX6-related_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 2,
    "not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B": 1,
    "not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders": 2,
    "not_provided|Heimler_syndrome_2|Peroxisome_biogenesis_disorder|PEX6-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 1,
    "PEX6-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder": 2,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder": 2,
    "Heimler_syndrome_2|not_specified|not_provided|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "not_specified|Peroxisome_biogenesis_disorder": 4,
    "Inborn_genetic_diseases|PEX6-related_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|not_provided": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 4,
    "Inborn_genetic_diseases|not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|PEX6-related_disorder|not_specified|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder": 1,
    "PEX6-related_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Retinal_dystrophy|not_specified|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_provided|PEX6-related_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder|Inborn_genetic_diseases": 1,
    "PEX6-related_disorder|Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|Heimler_syndrome_2": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|PEX6-related_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|Heimler_syndrome_2": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 7,
    "PEX6-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 2,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Hypotonia|Megalencephaly|Global_developmental_delay|CNS_demyelination|Leukodystrophy": 1,
    "PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_4A_(Zellweger)|PEX6-related_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|not_specified": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Zellweger_spectrum_disorders|Inborn_genetic_diseases|Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 1,
    "not_provided|PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Zellweger_spectrum_disorders|not_provided": 1,
    "PEX6-related_disorder|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Heimler_syndrome_2|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_specified|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_4B|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "PEX6-related_disorder|Heimler_syndrome_2": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|Heimler_syndrome_2": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Zellweger_spectrum_disorders": 2,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|PEX6-related_disorder|not_provided": 1,
    "PEX6-related_disorder|Inborn_genetic_diseases": 1,
    "PEX6-related_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_2|PEX6-related_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Zellweger_spectrum_disorders|not_provided": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|PEX6-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder": 1,
    "PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2": 2,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 1,
    "PEX6-related_disorder|not_provided|Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_2B": 676,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_2|not_provided": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|not_specified|not_provided": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Heimler_syndrome_2": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 2,
    "not_provided|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|Heimler_syndrome_2": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|not_provided|PEX6-related_disorder": 1,
    "not_provided|PEX6-related_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|not_specified|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder|not_specified": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_specified|Peroxisome_biogenesis_disorder|not_provided": 1,
    "not_specified|PEX6-related_disorder|Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|PEX6-related_disorder|Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|not_specified|Zellweger_spectrum_disorders|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|PEX6-related_disorder": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|PEX6-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders|not_provided": 1,
    "Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|not_specified|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|not_provided|not_specified": 1,
    "Heimler_syndrome_2|not_provided": 1,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_provided|not_specified|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders": 3,
    "Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_specified": 1,
    "Peroxisome_biogenesis_disorder|not_provided|PEX6-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_provided|PEX6-related_disorder|Peroxisome_biogenesis_disorder": 1,
    "PEX6-related_disorder|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Zellweger_spectrum_disorders|Heimler_syndrome_2|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder": 2,
    "PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|not_provided": 1,
    "Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Sensorineural_hearing_loss_disorder|Premature_ovarian_insufficiency|Paroxysmal_dystonia|Cognitive_impairment|Cerebellar_ataxia|Peripheral_neuropathy|not_specified": 1,
    "not_provided|Zellweger_spectrum_disorders": 16,
    "Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder|PEX6-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B|not_provided": 1,
    "Heimler_syndrome_2|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4B": 1,
    "Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|PEX6-related_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|PEX6-related_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|not_specified|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|not_specified|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|not_provided": 1,
    "PEX6-related_disorder|Heimler_syndrome_2|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B": 1,
    "Inborn_genetic_diseases|PEX6-related_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder|not_provided|Inborn_genetic_diseases": 1,
    "PEX6-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided": 7,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder_4A_(Zellweger)|Peroxisome_biogenesis_disorder_4B|Heimler_syndrome_2": 1,
    "not_provided|Hogue-Janssens_syndrome_1": 6,
    "not_provided|PPP2R5D-related_disorder": 5,
    "Hogue-Janssens_syndrome_1": 25,
    "Hogue-Janssens_syndrome_1|not_provided": 10,
    "PPP2R5D-related_disorder": 3,
    "Hogue-Janssens_syndrome_1|Inborn_genetic_diseases": 1,
    "PPP2R5D-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Encephalopathy": 1,
    "Hogue-Janssens_syndrome_1|not_provided|PPP2R5D-related_disorder": 1,
    "Inborn_genetic_diseases|Hogue-Janssens_syndrome_1|not_provided|Global_developmental_delay|See_cases|Neurodevelopmental_delay|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Hogue-Janssens_syndrome_1|not_provided|PPP2R5D-related_disorder": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Hogue-Janssens_syndrome_1|not_provided": 1,
    "Hogue-Janssens_syndrome_1|Genetic_developmental_and_epileptic_encephalopathy|not_provided": 1,
    "PPP2R5D-related_disorder|not_provided": 4,
    "Hogue-Janssens_syndrome_1|Intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "Hogue-Janssens_syndrome_1|Neurodevelopmental_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hogue-Janssens_syndrome_1|not_provided|Seizure": 1,
    "Neurodevelopmental_abnormality|Hogue-Janssens_syndrome_1|not_provided": 1,
    "not_provided|Hogue-Janssens_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hogue-Janssens_syndrome_1|not_provided": 2,
    "not_provided|PPP2R5D-related_disorder|not_specified": 1,
    "Hogue-Janssens_syndrome_1|PPP2R5D-related_disorder|not_provided": 1,
    "Neurodevelopmental_delay|Hogue-Janssens_syndrome_1": 1,
    "Inborn_genetic_diseases|PPP2R5D-related_disorder|not_provided": 1,
    "not_provided|3M_syndrome_1": 34,
    "3M_syndrome_1|not_provided": 24,
    "3M_syndrome_1|not_provided|not_specified": 4,
    "3M_syndrome_1|Inborn_genetic_diseases": 4,
    "not_provided|CUL7-related_disorder": 8,
    "not_provided|3M_syndrome_1|not_specified": 6,
    "CUL7-related_disorder": 8,
    "not_provided|3M_syndrome_1|3-M_syndrome": 2,
    "not_specified|not_provided|3M_syndrome_1": 3,
    "3M_syndrome_1|Inborn_genetic_diseases|not_provided": 7,
    "3M_syndrome_1|not_provided|CUL7-related_disorder": 2,
    "Inborn_genetic_diseases|3-M_syndrome|not_provided|not_specified": 1,
    "CUL7-related_disorder|not_provided": 7,
    "Yakut_short_stature_syndrome": 1,
    "CUL7-related_disorder|not_provided|3M_syndrome_1": 1,
    "CUL7-related_disorder|3M_syndrome_1": 1,
    "not_provided|not_specified|3M_syndrome_1": 4,
    "3-M_syndrome|3M_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|3M_syndrome_1|not_specified": 1,
    "3M_syndrome_1|CUL7-related_disorder": 1,
    "not_specified|3M_syndrome_1|not_provided": 4,
    "Inborn_genetic_diseases|3M_syndrome_1": 2,
    "3M_syndrome_1|not_specified|not_provided|CUL7-related_disorder": 1,
    "Inborn_genetic_diseases|CUL7-related_disorder": 1,
    "not_provided|3M_syndrome_1|CUL7-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|3M_syndrome_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|3M_syndrome_1|3-M_syndrome": 1,
    "CUL7-related_disorder|not_specified|not_provided|3M_syndrome_1": 1,
    "not_provided|not_specified|CUL7-related_disorder|3M_syndrome_1": 1,
    "not_provided|3M_syndrome_1|Growth_delay|Short_stature|not_specified": 1,
    "3M_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|3M_syndrome_1|not_provided": 1,
    "not_provided|3-M_syndrome|3M_syndrome_1": 1,
    "not_specified|not_provided|CUL7-related_disorder|3M_syndrome_1": 1,
    "3M_syndrome_1|CUL7-related_disorder|not_provided": 1,
    "not_provided|CUL7-related_disorder|Inborn_genetic_diseases": 2,
    "CUL7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|3M_syndrome_1": 2,
    "not_provided|CUL7-related_disorder|3M_syndrome_1": 1,
    "Early-childhood-onset_neurodegeneration_with_retinitis_pigmentosa|_sensorineural_hearing_loss|_and_demyelinating_peripheral_neuropathy": 1,
    "PTK7-related_disorder": 10,
    "not_provided|PTK7-related_disorder": 1,
    "PTK7-related_disorder|not_provided": 1,
    "CUL9-related_disorder": 48,
    "not_provided|CUL9-related_disorder": 4,
    "CUL9-related_disorder|not_provided": 4,
    "Arthritis|Ventricular_septal_defect|2-3_toe_syndactyly|Delayed_skeletal_maturation|Peripheral_pulmonary_artery_stenosis|Intellectual_disability|_moderate|Imperforate_anus|Coronary_artery_atherosclerosis|Abnormal_facial_shape|Psoriasiform_dermatitis|Vertebral_fusion|Absent/hypoplastic_coccyx|Single_umbilical_artery|Atrial_septal_defect|Delayed_speech_and_language_development": 2,
    "not_specified|CUL9-related_disorder": 2,
    "Autism|Mild_global_developmental_delay|Anxiety|Joint_laxity|Delayed_speech_and_language_development|Autistic_behavior": 1,
    "Treacher_Collins_Syndrome|_Recessive": 2,
    "Treacher_Collins_syndrome_3": 9,
    "not_provided|Treacher_Collins_syndrome_3": 8,
    "POLR1C-related_disorder|Treacher_Collins_syndrome_3": 1,
    "POLR1C-related_disorder|not_specified|not_provided|Treacher_Collins_syndrome_3": 1,
    "POLR1C-related_disorder|not_provided": 4,
    "Hypomyelinating_leukodystrophy_11": 20,
    "Inborn_genetic_diseases|Treacher_Collins_syndrome_3": 2,
    "Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11": 15,
    "Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Treacher_Collins_Syndrome|_Recessive": 1,
    "not_provided|POLR1C-related_disorder": 1,
    "not_provided|Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3": 4,
    "not_specified|Hypomyelinating_leukodystrophy_11": 1,
    "Hypomyelinating_leukodystrophy_11|not_provided": 7,
    "not_provided|Hypomyelinating_leukodystrophy_11": 2,
    "Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11|not_specified|not_provided": 1,
    "Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11|POLR1C-related_disorder|not_specified|Hearing_impairment|not_provided|Inborn_genetic_diseases": 1,
    "Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11|not_provided": 1,
    "Hypomyelinating_leukodystrophy_11|not_provided|Treacher_Collins_syndrome_3": 1,
    "Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3|POLR1C-related_disorder": 1,
    "Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3": 2,
    "Inborn_genetic_diseases|not_provided|Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11": 1,
    "Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11|not_provided|POLR1C-related_disorder": 1,
    "POLR1C-related_disorder": 7,
    "Treacher_Collins_syndrome_3|not_provided|Inborn_genetic_diseases": 1,
    "POLR1C-related_disorder|not_provided|Treacher_Collins_syndrome_3": 2,
    "not_provided|Treacher_Collins_syndrome_3|POLR1C-related_disorder": 1,
    "not_specified|Treacher_Collins_syndrome_3|not_provided": 1,
    "Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3|not_provided": 2,
    "Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3|not_provided|POLR1C-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Treacher_Collins_syndrome_3": 1,
    "Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3|not_provided|not_specified": 1,
    "not_provided|Treacher_Collins_syndrome_3|Hypomyelinating_leukodystrophy_11": 1,
    "Treacher_Collins_syndrome_3|not_provided": 1,
    "XPO5-related_disorder": 13,
    "not_provided|XPO5-related_disorder": 11,
    "XPO5-related_disorder|not_provided": 9,
    "XPO5-related_disorder|not_provided|not_specified": 1,
    "not_specified|XPO5-related_disorder|not_provided": 1,
    "not_provided|not_specified|XPO5-related_disorder": 1,
    "Xeroderma_pigmentosum_variant_type": 188,
    "Xeroderma_pigmentosum_variant_type|Xeroderma_pigmentosum|not_provided": 2,
    "POLH-related_disorder|not_provided": 1,
    "Xeroderma_pigmentosum_variant_type|not_provided": 12,
    "Xeroderma_pigmentosum|Inborn_genetic_diseases": 3,
    "not_provided|Xeroderma_pigmentosum_variant_type": 17,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum_variant_type|not_provided": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum_variant_type|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum_variant_type|See_cases": 1,
    "Xeroderma_pigmentosum_variant_type|Inborn_genetic_diseases": 1,
    "not_provided|Xeroderma_pigmentosum_variant_type|Xeroderma_pigmentosum": 3,
    "POLH-related_disorder|not_provided|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum_variant_type": 1,
    "Xeroderma_pigmentosum_variant_type|not_provided|POLH-related_disorder": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_variant_type|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_variant_type": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|Xeroderma_pigmentosum_variant_type": 1,
    "not_provided|Xeroderma_pigmentosum_variant_type|not_specified": 1,
    "Xeroderma_pigmentosum_variant_type|not_provided|not_specified": 2,
    "POLH-related_disorder|not_provided|Xeroderma_pigmentosum_variant_type|Xeroderma_pigmentosum": 1,
    "not_specified|POLH-related_disorder|not_provided|Xeroderma_pigmentosum_variant_type|Xeroderma_pigmentosum": 1,
    "POLH-related_disorder|Xeroderma_pigmentosum_variant_type|Xeroderma_pigmentosum|not_provided": 1,
    "not_specified|not_provided|Xeroderma_pigmentosum_variant_type": 1,
    "not_provided|POLH-related_disorder": 1,
    "Xeroderma_pigmentosum_variant_type|POLH-related_disorder|Xeroderma_pigmentosum|not_provided": 1,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum_variant_type": 1,
    "not_specified|Xeroderma_pigmentosum_variant_type|not_provided": 1,
    "Jaberi-Elahi_syndrome": 14,
    "GTPBP2-related_disorder|not_provided": 3,
    "Jaberi-Elahi_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Jaberi-Elahi_syndrome": 1,
    "GTPBP2-related_disorder": 2,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_12": 2,
    "Primary_ciliary_dyskinesia|RSPH9-related_disorder": 2,
    "Primary_ciliary_dyskinesia_12": 15,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_12": 7,
    "RSPH9-related_disorder": 2,
    "not_specified|Primary_ciliary_dyskinesia_12|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia_12|Primary_ciliary_dyskinesia": 3,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_12|not_provided": 1,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_12": 1,
    "RSPH9-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_12": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_12": 1,
    "Primary_ciliary_dyskinesia_12|not_provided|Primary_ciliary_dyskinesia": 1,
    "Atherosclerosis|_susceptibility_to": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_1|not_provided": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_1": 3,
    "VEGFA-related_disorder": 5,
    "not_provided|VEGFA-related_disorder": 2,
    "DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_118|Rare_epilepsy|TMEM63B-associated_disorder|not_provided": 1,
    "TMEM63B-related_condition": 1,
    "DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_118": 1,
    "Inborn_genetic_diseases|DEVELOPMENTAL_AND_EPILEPTIC_ENCEPHALOPATHY_118": 2,
    "TMEM63B-related_Neurodevelopmental_disorder": 1,
    "Carey-Fineman-Ziter_syndrome_2": 3,
    "SLC29A1-related_disorder": 2,
    "Hemolytic_disease_of_fetus_OR_newborn_due_to_isoimmunization": 1,
    "Leukodystrophy|_hypomyelinating|_26|_with_chondrodysplasia": 2,
    "Leukodystrophy|_hypomyelinating|_26|_with_chondrodysplasia|Primary_bone_dysplasia_with_multiple_joint_dislocations": 1,
    "not_specified|Hypomyelinating_leukodystrophy_11|Treacher_Collins_syndrome_3": 1,
    "TCTE1-related_disorder": 2,
    "Combined_oxidative_phosphorylation_defect_type_8": 74,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8": 17,
    "not_provided|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "AARS2-related_disorder|not_provided": 2,
    "not_provided|Leukoencephalopathy|_progressive|_with_ovarian_failure|Combined_oxidative_phosphorylation_defect_type_8|Inborn_genetic_diseases": 1,
    "not_specified|Leukoencephalopathy|_progressive|_with_ovarian_failure|not_provided|Combined_oxidative_phosphorylation_defect_type_8": 2,
    "not_provided|Mitochondrial_disease": 16,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_8": 5,
    "Combined_oxidative_phosphorylation_defect_type_8|not_provided|AARS2-related_disorder": 1,
    "not_provided|Leukoencephalopathy|_progressive|_with_ovarian_failure|Combined_oxidative_phosphorylation_defect_type_8": 2,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_8": 4,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|not_specified|AARS2-related_disorder": 1,
    "Leukoencephalopathy|_progressive|_with_ovarian_failure|not_provided": 3,
    "Leukoencephalopathy|_progressive|_with_ovarian_failure|Combined_oxidative_phosphorylation_defect_type_8|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_8|not_provided|not_specified": 2,
    "not_provided|AARS2-related_disorder": 3,
    "Combined_oxidative_phosphorylation_defect_type_8|Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|not_specified|not_provided|AARS2-related_disorder": 1,
    "Leukoencephalopathy|_progressive|_with_ovarian_failure": 12,
    "Combined_oxidative_phosphorylation_defect_type_8|not_specified|not_provided": 5,
    "AARS2-related_disorder": 7,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|Cardiovascular_phenotype": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|Leukoencephalopathy|_progressive|_with_ovarian_failure|not_provided": 1,
    "AARS2-related_disorder|not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_8": 2,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_8": 2,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_8|not_provided": 3,
    "Combined_oxidative_phosphorylation_defect_type_8|not_provided": 3,
    "Combined_oxidative_phosphorylation_defect_type_8|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|AARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|AARS2-related_disorder": 1,
    "AARS2-related_disorder|Leukoencephalopathy|_progressive|_with_ovarian_failure|Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_8|Mitochondrial_disease|Pulmonary_hypoplasia": 1,
    "AARS2-related_disorder|not_specified": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|not_specified|AARS2-related_disorder|Leukoencephalopathy|_progressive|_with_ovarian_failure|not_provided": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_8|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Inborn_genetic_diseases": 2,
    "Leukoencephalopathy|_progressive|_with_ovarian_failure|not_provided|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "Combined_oxidative_phosphorylation_deficiency|Combined_oxidative_phosphorylation_defect_type_8|not_provided": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_8": 2,
    "Combined_oxidative_phosphorylation_defect_type_8|not_provided|Leukoencephalopathy|_progressive|_with_ovarian_failure|not_specified": 1,
    "Inborn_genetic_diseases|Cardiovascular_phenotype": 10,
    "not_specified|not_provided|AARS2-related_disorder": 1,
    "not_specified|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_8|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|AARS2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|Inborn_genetic_diseases|not_provided|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "Leukoencephalopathy|_progressive|_with_ovarian_failure|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "Leukoencephalopathy|_progressive|_with_ovarian_failure|not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "Mitochondrial_disease|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|not_provided|not_specified|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "AARS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|AARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "AARS2-related_disorder|not_provided|not_specified": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|Pulmonary_hypoplasia": 1,
    "Cardiovascular_phenotype|Leukoencephalopathy|_progressive|_with_ovarian_failure|Combined_oxidative_phosphorylation_defect_type_8|Inborn_genetic_diseases|Generalized_muscle_weakness|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_8|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Iron_accumulation_in_brain": 1,
    "not_specified|not_provided|Leukoencephalopathy|_progressive|_with_ovarian_failure|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "not_specified|AARS2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_disease|Combined_oxidative_phosphorylation_defect_type_8": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|not_specified|Leukoencephalopathy|_progressive|_with_ovarian_failure": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_8|Inborn_genetic_diseases": 1,
    "CDC5L-related_disorder": 16,
    "CDC5L-related_disorder|not_provided": 1,
    "CDC5L-related_disorder|not_specified": 1,
    "Cleidocranial_dysostosis": 127,
    "Cleidocranial_dysostosis|not_provided": 8,
    "not_provided|Cleidocranial_dysostosis": 11,
    "Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome|Cleidocranial_dysostosis": 2,
    "Cleidocranial_dysostosis|Inborn_genetic_diseases|not_provided": 1,
    "RUNX2-related_disorder|not_provided": 5,
    "RUNX2-related_disorder": 9,
    "Inborn_genetic_diseases|not_provided|Cleidocranial_dysostosis": 2,
    "RUNX2-related_disorder|not_specified|not_provided": 1,
    "Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome|Cleidocranial_dysostosis|not_provided": 2,
    "not_specified|not_provided|Cleidocranial_dysostosis": 1,
    "Cleidocranial_dysplasia_1|_forme_fruste|_with_brachydactyly": 1,
    "Cleidocranial_dysostosis|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome": 2,
    "Cleidocranial_dysostosis|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Cleidocranial_dysostosis": 1,
    "not_provided|Cleidocranial_dysostosis|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome|not_specified": 1,
    "not_provided|RUNX2-related_disorder|Cleidocranial_dysostosis|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome": 1,
    "Cleidocranial_dysostosis|not_provided|RUNX2-related_disorder": 2,
    "Cleidocranial_dysostosis|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome|not_provided": 1,
    "RUNX2-related_disorder|not_provided|Cleidocranial_dysostosis": 1,
    "Cleidocranial_dysostosis|not_provided|Cleidocranial_dysplasia_1|_forme_fruste|_dental_anomalies_only": 1,
    "Cleidocranial_dysostosis|RUNX2-related_disorder|not_provided|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome": 1,
    "not_provided|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome": 2,
    "Cleidocranial_dysostosis|Inborn_genetic_diseases": 1,
    "Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome|not_provided|Cleidocranial_dysostosis": 1,
    "not_provided|Cleidocranial_dysostosis|Metaphyseal_dysplasia-maxillary_hypoplasia-brachydacty_syndrome": 1,
    "CLIC5-related_disorder": 1,
    "not_provided|not_specified|CLIC5-related_disorder": 5,
    "not_provided|CLIC5-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_103": 3,
    "CLIC5-related_disorder|not_specified|not_provided": 1,
    "not_provided|CLIC5-related_disorder": 6,
    "CLIC5-related_disorder|not_provided": 3,
    "not_specified|not_provided|CLIC5-related_disorder": 2,
    "not_provided|CLIC5-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_103": 1,
    "not_specified|CLIC5-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_103|not_specified|not_provided": 1,
    "TDRD6-related_disorder": 6,
    "not_provided|TDRD6-related_disorder": 1,
    "PLA2G7-related_disorder|not_provided|RECLASSIFIED_-_MYOC_POLYMORPHISM": 1,
    "Platelet-activating_factor_acetylhydrolase_deficiency": 7,
    "not_specified|PLA2G7-related_disorder": 1,
    "PLA2G7-related_disorder|not_provided|Platelet-activating_factor_acetylhydrolase_deficiency": 1,
    "Platelet-activating_factor_acetylhydrolase_deficiency|not_specified|PLA2G7-related_disorder": 1,
    "PLA2G7-related_disorder|RECLASSIFIED_-_MYOC_POLYMORPHISM": 1,
    "PLA2G7-related_disorder|not_provided": 1,
    "not_specified|Platelet-activating_factor_acetylhydrolase_deficiency": 1,
    "PLA2G7-related_disorder": 2,
    "TNFRSF21-related_condition": 1,
    "not_specified|TNFRSF21-related_condition": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 19,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 120,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided": 26,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 4,
    "CD2AP-related_disorder": 6,
    "Corticosteroids_response|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "Inborn_genetic_diseases|CD2AP-related_disorder": 2,
    "CD2AP-related_disorder|not_provided": 4,
    "CD2AP-related_disorder|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 3,
    "not_provided|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|CD2AP-related_disorder": 3,
    "CD2AP-related_disorder|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|Focal_segmental_glomerulosclerosis_3": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_specified": 1,
    "Inherited_focal_segmental_glomerulosclerosis": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_specified|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided|not_specified": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided": 1,
    "Inherited_focal_segmental_glomerulosclerosis|not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Inherited_focal_segmental_glomerulosclerosis": 1,
    "Inherited_focal_segmental_glomerulosclerosis|not_provided|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "not_provided|not_specified|Kidney_disorder|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided|CD2AP-related_disorder": 1,
    "not_provided|CD2AP-related_disorder|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "Focal_segmental_glomerulosclerosis_3|_susceptibility_to|not_provided|Focal_segmental_glomerulosclerosis_3": 1,
    "not_specified|Focal_segmental_glomerulosclerosis|not_provided|Focal_segmental_glomerulosclerosis_3|_susceptibility_to": 1,
    "not_provided|Focal_segmental_glomerulosclerosis": 10,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 155,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 56,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 40,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|not_specified": 4,
    "not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 6,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 9,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Abnormality_of_metabolism/homeostasis": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(-)_TYPE": 1,
    "METHYLMALONIC_ACIDURIA|_mut(0)_TYPE|not_provided": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_specified": 3,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified|not_provided": 2,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 5,
    "Methylmalonic_aciduria|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 49,
    "MMUT-related_disorder|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified": 5,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 5,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_specified|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 3,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|not_specified": 2,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder_8B|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified|not_provided": 1,
    "not_provided|MMUT-related_disorder": 1,
    "METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "not_provided|Methylmalonic_acidemia": 8,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 4,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE|MMUT-related_disorder|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_specified|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 2,
    "MMUT-related_disorder|not_provided|not_specified": 2,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided": 11,
    "not_provided|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "MMUT-related_disorder|not_provided": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "MMUT-related_disorder|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 2,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia": 3,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|not_specified": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified|not_provided": 3,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder|not_provided": 1,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia": 2,
    "not_specified|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|not_provided": 1,
    "Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_specified": 1,
    "Methylmalonic_aciduria|MMUT-related_disorder|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "not_provided|not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder|not_provided": 2,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 2,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 5,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 6,
    "Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided": 4,
    "not_provided|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder|not_provided": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified": 2,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 2,
    "Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "not_specified|not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|MMUT-related_disorder|not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder": 1,
    "MMUT-related_disorder": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 2,
    "Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "METHYLMALONIC_ACIDURIA|_mut(-)_TYPE": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|not_provided": 1,
    "Methylmalonic_acidemia|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "MMUT-related_disorder|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_provided": 1,
    "not_provided|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 1,
    "not_provided|not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia|Abnormality_of_metabolism/homeostasis": 1,
    "not_provided|not_specified|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder": 1,
    "Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(-)_TYPE|not_provided": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE|not_provided": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "MMUT-related_disorder|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_specified|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder|not_specified": 1,
    "MMUT-related_disorder|Methylmalonic_acidemia|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|MMUT-related_disorder|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided": 2,
    "not_specified|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|not_specified": 1,
    "not_provided|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|See_cases|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_acidemia|not_provided|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "Methylmalonic_acidemia|not_provided|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency": 1,
    "Methylmalonic_aciduria_due_to_complete_methylmalonyl-CoA_mutase_deficiency|Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|METHYLMALONIC_ACIDURIA|_mut(0)_TYPE": 1,
    "Rh-null|_regulator_type": 5,
    "RHAG-related_disorder": 3,
    "Rh-null|_regulator_type|not_specified": 1,
    "Rh_deficiency_syndrome|Rh-null|_regulator_type": 1,
    "RHAG-related_disorder|not_provided": 2,
    "not_specified|RHAG-related_disorder|not_provided": 1,
    "Overhydrated_hereditary_stomatocytosis": 3,
    "not_provided|not_specified|Overhydrated_hereditary_stomatocytosis": 1,
    "Rh_mod_blood_group_phenotype": 3,
    "Overhydrated_hereditary_stomatocytosis|Rh-null|_regulator_type": 3,
    "not_provided|Rh-null|_regulator_type|Overhydrated_hereditary_stomatocytosis": 1,
    "RHAG-related_disorder|not_provided|not_specified": 1,
    "not_provided|Overhydrated_hereditary_stomatocytosis": 1,
    "Rh-null|_regulator_type|Overhydrated_hereditary_stomatocytosis|RHAG-related_disorder|not_provided": 1,
    "not_provided|not_specified|altered_red_cell_phenotype": 1,
    "not_provided|RHAG-related_disorder": 1,
    "Char_syndrome|not_provided": 7,
    "not_provided|Patent_ductus_arteriosus_2": 1,
    "Char_syndrome|Patent_ductus_arteriosus_2": 3,
    "Inborn_genetic_diseases|not_provided|Char_syndrome": 1,
    "TFAP2B-related_disorder": 3,
    "Char_syndrome": 27,
    "Patent_ductus_arteriosus_2": 2,
    "not_provided|Char_syndrome": 2,
    "not_provided|Char_syndrome|not_specified": 1,
    "Char_syndrome|Hypertelorism|Bifid_nasal_tip|Opacification_of_the_corneal_stroma|Clinodactyly_of_the_5th_finger|Upslanted_palpebral_fissure": 1,
    "Patent_ductus_arteriosus_2|Char_syndrome": 1,
    "TFAP2B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease": 71,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided": 70,
    "Polycystic_kidney_disease_4|not_provided": 36,
    "Polycystic_kidney_disease_4": 820,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 48,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided": 17,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_provided": 18,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases": 8,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 198,
    "Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder": 2,
    "PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease": 15,
    "Polycystic_kidney_disease_4|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 17,
    "not_specified|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_provided": 1,
    "not_provided|not_specified|Kidney_failure|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease": 1,
    "PKHD1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 165,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease": 6,
    "not_provided|Polycystic_kidney_disease_4": 46,
    "Polycystic_kidney_disease_4|not_specified|Autosomal_recessive_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 12,
    "PKHD1-related_disorder": 74,
    "Polycystic_kidney_disease|Inborn_genetic_diseases": 4,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 5,
    "Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 23,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 16,
    "Polycystic_kidney_disease_4|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 16,
    "Polycystic_kidney_disease_4|not_specified": 3,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|PKHD1-related_disorder": 6,
    "not_provided|PKHD1-related_disorder": 3,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided": 19,
    "not_provided|Polycystic_kidney_disease_4|not_specified|Autosomal_recessive_polycystic_kidney_disease": 2,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 3,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4": 7,
    "not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 14,
    "Inborn_genetic_diseases|PKHD1-related_disorder": 4,
    "not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 17,
    "Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 28,
    "not_specified|not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 5,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|not_provided": 5,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 5,
    "Enlarged_kidney|Hyperechogenic_kidneys|Anhydramnios": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 20,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4": 18,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified": 9,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided": 9,
    "not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 9,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_specified": 3,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4": 12,
    "not_provided|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|Autosomal_recessive_polycystic_kidney_disease": 2,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease": 14,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder": 10,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 7,
    "Abnormality_of_the_genitourinary_system|Polycystic_kidney_disease_4": 2,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided": 2,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease|not_provided": 6,
    "PKHD1-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases|not_provided": 5,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Biliary_tract_abnormality": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_4|not_provided": 2,
    "Inborn_genetic_diseases|PKHD1-related_disorder|Polycystic_kidney_disease_4|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 40,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4": 3,
    "PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|See_cases": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 3,
    "PKHD1-related_disorder|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease": 1,
    "not_provided|Polycystic_kidney_disease_4|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|See_cases": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Autosomal_dominant_polycystic_liver_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|not_provided|not_specified|Autosomal_recessive_polycystic_kidney_disease": 3,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|not_provided": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4|Inborn_genetic_diseases": 4,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|not_provided": 4,
    "PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 7,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4": 1,
    "Enlarged_kidney|Hyperechogenic_kidneys|Multiple_renal_cysts|Anhydramnios": 3,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|not_specified": 4,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease": 1,
    "Inborn_genetic_diseases|not_specified|PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 10,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Biliary_tract_abnormality|PKHD1-related_disorder": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 6,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Colon_cancer": 1,
    "not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 3,
    "not_provided|PKHD1-related_disorder|Polycystic_kidney_disease_4|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Renal_cyst|PKHD1-related_disorder|Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|not_provided": 2,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|Autosomal_recessive_polycystic_kidney_disease|not_provided": 1,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_liver_disease|PKHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 2,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 12,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4|PKHD1-related_disorder": 2,
    "not_provided|not_specified|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 2,
    "Polycystic_kidney_disease_4|not_provided|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 2,
    "PKHD1-related_disorder|not_specified|Autosomal_recessive_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Polycystic_kidney_disease_4": 7,
    "Autosomal_recessive_polycystic_kidney_disease|See_cases": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Biliary_tract_abnormality": 1,
    "not_specified|Polycystic_kidney_disease_4|not_provided": 1,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder": 1,
    "not_specified|Polycystic_kidney_disease_4|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|not_specified|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 5,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 4,
    "Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided": 2,
    "not_specified|Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Autosomal_dominant_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_4|not_specified|Autosomal_recessive_polycystic_kidney_disease": 5,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_polycystic_kidney_disease": 3,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|not_specified": 5,
    "Familial_cystic_renal_disease": 5,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided": 2,
    "PKHD1-related_disorder|Polycystic_kidney_disease|Biliary_tract_abnormality|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Multiple_renal_cysts|Anhydramnios": 3,
    "Autosomal_recessive_polycystic_kidney_disease|Familial_cystic_renal_disease|not_provided": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_specified|not_provided": 4,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided": 2,
    "not_provided|not_specified|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_specified|Caroli_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_provided|not_specified": 3,
    "Autosomal_recessive_polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided|Autosomal_dominant_polycystic_liver_disease": 2,
    "Polycystic_kidney_disease|Hypoplastic_aortic_arch|not_provided|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|not_provided|not_specified": 1,
    "PKHD1-related_disorder|not_provided|Polycystic_kidney_disease_4": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease_4": 3,
    "Kidney_failure|Polycystic_kidney_disease_4|PKHD1-related_disorder|Autosomal_dominant_polycystic_liver_disease|not_specified|Caroli_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder|Polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 7,
    "Autosomal_dominant_polycystic_liver_disease|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease|Hypoplastic_aortic_arch": 2,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_specified": 2,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease_4": 3,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases": 1,
    "PKHD1-related_disorder|not_specified|Autosomal_recessive_polycystic_kidney_disease": 3,
    "Abnormality_of_the_genitourinary_system|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_specified": 2,
    "PKHD1-related_disorder|not_specified|not_provided|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4": 2,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|not_specified": 2,
    "PKHD1-related_disorder|not_specified|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 3,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_4": 2,
    "Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4": 3,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided|PKHD1-related_disorder": 3,
    "PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease": 1,
    "not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_specified": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4|not_provided": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|PKHD1-related_disorder|Polycystic_kidney_disease_4": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 3,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder": 4,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|PKHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Renal_cyst": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided|PKHD1-related_disorder": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder": 5,
    "not_specified|PKHD1-related_disorder": 1,
    "not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease_4|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease_4|Inborn_genetic_diseases": 1,
    "Caroli_disease": 1,
    "not_provided|PKHD1-related_disorder|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 2,
    "Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|not_provided": 2,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided|Autosomal_dominant_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 2,
    "PKHD1-related_disorder|not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder|not_specified": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease|See_cases": 1,
    "not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Renal_cyst|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_specified": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease|Ventricular_hypertrophy|Renal_cyst": 1,
    "Polycystic_kidney_disease_4|Polycystic_kidney_disease": 2,
    "Classic_homocystinuria": 120,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|PKHD1-related_disorder|Caroli_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease|Renal_cyst|Polycystic_kidney_disease|Abnormal_intrahepatic_bile_duct_morphology": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided|not_specified": 1,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases|not_provided|Autosomal_recessive_polycystic_kidney_disease": 4,
    "PKHD1-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "Inborn_genetic_diseases|PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 2,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|not_provided": 1,
    "Polycystic_kidney_disease_4|Inborn_genetic_diseases|not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|PKHD1-related_disorder|not_provided": 1,
    "not_provided|PKHD1-related_disorder|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease_4|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 2,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_provided|Inborn_genetic_diseases": 1,
    "PKHD1-related_disorder|not_specified|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "not_specified|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease|Biliary_tract_abnormality": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_liver_disease|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "not_specified|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4|not_specified": 2,
    "PKHD1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Biliary_tract_abnormality|Polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_polycystic_kidney_disease": 2,
    "Polycystic_kidney_disease_4|Caroli_disease|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|_with_or_without_hepatic_disease": 1,
    "PKHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_polycystic_kidney_disease": 3,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_4": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|Inborn_genetic_diseases": 2,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Polycystic_kidney_disease_4|PKHD1-related_disorder": 2,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_specified": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease": 1,
    "Autosomal_recessive_polycystic_kidney_disease|not_provided|Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|Ventricular_hypertrophy|Renal_cyst": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Oligohydramnios|Periportal_fibrosis": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|not_provided|Caroli_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|Biliary_tract_abnormality": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_provided|not_specified": 1,
    "Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_specified|Autosomal_recessive_polycystic_kidney_disease|not_provided|PKHD1-related_disorder": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Polycystic_kidney_disease": 2,
    "Autosomal_dominant_polycystic_liver_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Hereditary_disease|Polycystic_kidney_disease_4|not_provided": 1,
    "Inborn_genetic_diseases|PKHD1-related_disorder|not_provided|not_specified|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease_4|not_provided|PKHD1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Autosomal_dominant_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Autosomal_dominant_polycystic_liver_disease": 1,
    "Anhydramnios|Hyperechogenic_kidneys|Multiple_renal_cysts|Enlarged_kidney": 1,
    "Polycystic_kidney_disease_4|not_specified|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|not_specified": 1,
    "not_provided|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder|Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "PKHD1-related_disorder|not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease_4": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|not_provided|PKHD1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_polycystic_kidney_disease|not_provided|PKHD1-related_disorder": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease_4|PKHD1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided|PKHD1-related_disorder": 2,
    "not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "PKHD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "PKHD1-related_disorder|not_provided": 1,
    "Autosomal_dominant_polycystic_liver_disease|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_provided|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease|See_cases|Biliary_tract_abnormality": 1,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|PKHD1-related_disorder|not_provided|Autosomal_recessive_polycystic_kidney_disease": 2,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|PKHD1-related_disorder": 1,
    "Inborn_genetic_diseases|Prostate_cancer|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_specified|Polycystic_kidney_disease_4|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease|not_provided": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided": 1,
    "Polycystic_kidney_disease_4|Abnormal_intrahepatic_bile_duct_morphology|See_cases|Autosomal_recessive_polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|not_provided|Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease|not_specified|PKHD1-related_disorder|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Biliary_tract_abnormality": 3,
    "Autosomal_recessive_polycystic_kidney_disease|not_specified|not_provided|PKHD1-related_disorder": 1,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_4|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Autosomal_recessive_polycystic_kidney_disease|PKHD1-related_disorder": 1,
    "PKHD1-related_disorder|Polycystic_kidney_disease_4|not_provided|not_specified|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease_4|Autosomal_recessive_polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_4|Autosomal_dominant_polycystic_liver_disease|PKHD1-related_disorder|Inborn_genetic_diseases|not_provided|Colorectal_cancer|_protection_against|Autosomal_recessive_polycystic_kidney_disease|Periportal_fibrosis|Oligohydramnios|Polycystic_kidney_disease|Renal_cyst|See_cases": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Polycystic_kidney_disease|Polycystic_kidney_disease_4": 1,
    "not_provided|Candidiasis|_familial|_6": 4,
    "Candidiasis|_familial|_6": 124,
    "not_specified|Candidiasis|_familial|_6": 8,
    "IL17F-related_disorder|not_provided|Candidiasis|_familial|_6": 1,
    "Candidiasis|_familial|_6|not_specified": 8,
    "Candidiasis|_familial|_6|not_provided": 1,
    "not_specified|not_provided|Candidiasis|_familial|_6": 1,
    "Candidiasis|_familial|_6|not_specified|not_provided": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 129,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_specified": 5,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 6,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_provided|not_specified": 3,
    "EFHC1-related_disorder|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_specified|not_provided|Juvenile_myoclonic_epilepsy": 2,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 38,
    "not_specified|Juvenile_myoclonic_epilepsy": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Juvenile_myoclonic_epilepsy|not_specified": 2,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_provided": 6,
    "not_provided|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 7,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Typical_absence_seizure": 11,
    "not_provided|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 5,
    "Juvenile_myoclonic_epilepsy|not_specified|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_provided": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_provided": 5,
    "Typical_absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 10,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Juvenile_myoclonic_epilepsy": 3,
    "not_specified|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 15,
    "Juvenile_myoclonic_epilepsy|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_provided": 1,
    "not_provided|Juvenile_myoclonic_epilepsy|Absence_seizure": 1,
    "not_provided|EFHC1-related_disorder|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_specified": 1,
    "not_specified|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 4,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_specified": 10,
    "EFHC1-related_disorder|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_specified|not_provided": 2,
    "Juvenile_myoclonic_epilepsy|not_specified|not_provided|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 1,
    "Absence_seizure": 2,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_specified|not_provided|Juvenile_myoclonic_epilepsy": 2,
    "Typical_absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_specified|Juvenile_myoclonic_epilepsy": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_specified|Juvenile_myoclonic_epilepsy|not_provided": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_specified|not_provided": 2,
    "Absence_seizure|Juvenile_myoclonic_epilepsy": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|EFHC1-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|EFHC1-related_disorder|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_7|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 1,
    "Epilepsy|_juvenile_absence|_susceptibility_to|_1|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 1,
    "Juvenile_myoclonic_epilepsy|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|EFHC1-related_disorder|not_specified|not_provided": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|EFHC1-related_disorder|Juvenile_myoclonic_epilepsy": 1,
    "not_specified|Typical_absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 1,
    "Juvenile_myoclonic_epilepsy|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_provided": 1,
    "not_provided|not_specified|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Juvenile_myoclonic_epilepsy": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|Juvenile_myoclonic_epilepsy|not_specified|not_provided": 1,
    "EFHC1-related_disorder": 1,
    "Absence_seizure|not_provided": 1,
    "not_provided|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|Seizure": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|EFHC1-related_disorder|not_provided": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_specified|not_provided": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Epilepsy|_juvenile_absence|_susceptibility_to|_1|Juvenile_myoclonic_epilepsy|not_provided|not_specified": 1,
    "not_provided|not_specified|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 1,
    "Juvenile_myoclonic_epilepsy|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_specified": 2,
    "Typical_absence_seizure|Juvenile_myoclonic_epilepsy": 1,
    "not_provided|Typical_absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_provided|not_specified|Juvenile_myoclonic_epilepsy": 1,
    "Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|not_provided|Juvenile_myoclonic_epilepsy": 1,
    "not_provided|not_specified|Absence_seizure|Juvenile_myoclonic_epilepsy|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Epilepsy|_juvenile_absence|_susceptibility_to|_1": 1,
    "Juvenile_myoclonic_epilepsy|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure": 1,
    "not_specified|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|EFHC1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Absence_seizure|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Juvenile_myoclonic_epilepsy": 1,
    "not_provided|not_specified|Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|Juvenile_myoclonic_epilepsy": 1,
    "Myoclonic_epilepsy|_juvenile|_susceptibility_to|_1|Absence_seizure|not_provided|EFHC1-related_disorder": 1,
    "Juvenile_myoclonic_epilepsy|Absence_seizure|not_provided": 1,
    "not_provided|Epilepsy|_juvenile_myoclonic|_susceptibility_to|_10": 1,
    "Epilepsy|_juvenile_myoclonic|_susceptibility_to|_10|not_provided": 3,
    "CILK1-related_disorder": 3,
    "CILK1-related_disorder|not_specified|not_provided": 2,
    "Epilepsy|_juvenile_myoclonic|_susceptibility_to|_10": 4,
    "Cranioectodermal_dysplasia|CRANIOECTODERMAL_DYSPLASIA_6": 1,
    "not_provided|CILK1-related_disorder|not_specified": 2,
    "not_provided|CILK1-related_disorder": 2,
    "not_specified|not_provided|Epilepsy|_juvenile_myoclonic|_susceptibility_to|_10": 1,
    "Endocrine-cerebro-osteodysplasia_syndrome|not_provided": 1,
    "Congenital_ocular_coloboma|Microphthalmia|Dysplastic_corpus_callosum|not_provided": 2,
    "not_specified|not_provided|CILK1-related_disorder": 1,
    "Epilepsy|_juvenile_myoclonic|_susceptibility_to|_10|Endocrine-cerebro-osteodysplasia_syndrome|CILK1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Endocrine-cerebro-osteodysplasia_syndrome": 2,
    "CILK1-related_disorder|not_provided|not_specified": 1,
    "Endocrine-cerebro-osteodysplasia_syndrome": 4,
    "not_provided|not_specified|CILK1-related_disorder": 1,
    "Endocrine-cerebro-osteodysplasia_syndrome|not_specified": 1,
    "CILK1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_38": 1,
    "Spinocerebellar_ataxia_type_38": 9,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_38": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_38": 1,
    "not_provided|Spinocerebellar_ataxia_type_38": 1,
    "Spinocerebellar_ataxia_type_38|not_specified|ELOVL5-related_disorder|not_provided": 1,
    "ELOVL5-related_disorder": 1,
    "not_provided|ELOVL5-related_disorder": 1,
    "Gamma-glutamylcysteine_synthetase_deficiency": 19,
    "Gamma-glutamylcysteine_synthetase_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|GCLC-related_disorder": 3,
    "not_provided|Gamma-glutamylcysteine_synthetase_deficiency": 2,
    "Gamma-glutamylcysteine_synthetase_deficiency|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|Gamma-glutamylcysteine_synthetase_deficiency": 1,
    "Inborn_genetic_diseases|Gamma-glutamylcysteine_synthetase_deficiency": 2,
    "GCLC-related_disorder|not_provided": 5,
    "Gamma-glutamylcysteine_synthetase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "GCLC-related_disorder": 1,
    "Myocardial_infarction|_susceptibility_to|not_provided": 1,
    "Myopathy_with_myalgia|_increased_serum_creatine_kinase|_and_with_or_without_episodic_rhabdomyolysis": 9,
    "MLIP-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|Myopathy_with_myalgia|_increased_serum_creatine_kinase|_and_with_or_without_episodic_rhabdomyolysis": 1,
    "HCRTR2-related_disorder": 6,
    "not_provided|HCRTR2-related_disorder": 1,
    "not_specified|HCRTR2-related_disorder|not_provided": 1,
    "BMP5-related_disorder": 10,
    "BMP5-related_disorder|not_provided": 2,
    "Microtia|Patellar_aplasia|Hypoplastic_ischiopubic_ramus|Atrioventricular_canal_defect": 2,
    "not_provided|BMP5-related_disorder": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1491,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 1199,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 16,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 7,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6": 45,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Inborn_genetic_diseases": 50,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|Inborn_genetic_diseases": 48,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 59,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_specified": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided": 69,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 63,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 67,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided": 39,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|DST-related_disorder|not_provided": 2,
    "DST-related_disorder|not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "DST-related_disorder": 24,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 24,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|DST-related_disorder": 10,
    "DST-related_disorder|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 3,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided": 5,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 7,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder": 9,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided|DST-related_disorder": 3,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|DST-related_disorder": 5,
    "DST-related_disorder|not_provided": 3,
    "DST-related_disorder|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 6,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Inborn_genetic_diseases|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 7,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|DST-related_disorder|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 3,
    "not_provided|DST-related_disorder|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 1,
    "DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided": 2,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided": 6,
    "Moyamoya_angiopathy|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 1,
    "not_provided|DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 3,
    "not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 5,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|DST-related_disorder|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 1,
    "not_specified|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 7,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Multiple_sclerosis": 1,
    "Multiple_sclerosis|Inborn_genetic_diseases|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|DST-related_disorder": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Inborn_genetic_diseases|DST-related_disorder": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Inborn_genetic_diseases": 6,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Multiple_sclerosis|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|Inborn_genetic_diseases|not_provided": 2,
    "Cardiomyopathy|Global_developmental_delay|Congenital_contracture|Hypotonia": 1,
    "not_provided|not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6": 3,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_specified|DST-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_specified": 3,
    "not_specified|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided|DST-related_disorder": 2,
    "not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|Charcot-Marie-Tooth_disease": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_specified|not_provided": 3,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_specified": 3,
    "DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_specified": 1,
    "DST-related_disorder|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_specified|not_provided": 2,
    "DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided|not_specified": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Multiple_sclerosis|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_specified|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Multiple_sclerosis|Inborn_genetic_diseases|not_provided|DST-related_disorder|not_specified": 1,
    "not_specified|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6": 2,
    "Multiple_sclerosis": 5,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided": 1,
    "Distal_spinal_muscular_atrophy|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Hereditary_sensory_and_autonomic_neuropathy_type_6|DST-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|not_provided|DST-related_disorder": 1,
    "not_provided|DST-related_disorder|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_6|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency|Multiple_sclerosis|not_provided": 1,
    "not_provided|DST-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_3|_localized_or_generalized_intermediate|_with_BP230_deficiency": 1,
    "DST-related_disorder|not_specified": 1,
    "DST-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_6|not_provided": 1,
    "KIAA1586-related_disorder": 4,
    "RAB23-related_Carpenter_syndrome": 61,
    "RAB23-related_Carpenter_syndrome|not_provided": 2,
    "Carpenter_syndrome": 135,
    "Carpenter_syndrome|not_provided": 5,
    "RAB23-related_Carpenter_syndrome|Carpenter_syndrome": 4,
    "See_cases|RAB23-related_Carpenter_syndrome|Carpenter_syndrome": 1,
    "RAB23-related_Carpenter_syndrome|Inborn_genetic_diseases": 2,
    "RAB23-related_Carpenter_syndrome|RAB23-related_disorder|Carpenter_syndrome": 6,
    "RAB23-related_disorder": 21,
    "not_specified|RAB23-related_Carpenter_syndrome|Carpenter_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|RAB23-related_disorder": 1,
    "Carpenter_syndrome|Inborn_genetic_diseases": 1,
    "RAB23-related_disorder|Carpenter_syndrome": 7,
    "RAB23-related_disorder|Carpenter_syndrome|RAB23-related_Carpenter_syndrome": 2,
    "not_provided|Carpenter_syndrome|Inborn_genetic_diseases|RAB23-related_Carpenter_syndrome|RAB23-related_disorder": 1,
    "RAB23-related_Carpenter_syndrome|RAB23-related_disorder": 2,
    "RAB23-related_Carpenter_syndrome|RAB23-related_disorder|not_provided|Carpenter_syndrome|Inborn_genetic_diseases": 1,
    "RAB23-related_Carpenter_syndrome|Carpenter_syndrome|RAB23-related_disorder": 4,
    "RAB23-related_disorder|not_specified": 1,
    "not_provided|Carpenter_syndrome": 2,
    "Carpenter_syndrome|Inborn_genetic_diseases|RAB23-related_disorder": 1,
    "Carpenter_syndrome|RAB23-related_disorder|not_provided|Inborn_genetic_diseases|RAB23-related_Carpenter_syndrome": 1,
    "RAB23-related_disorder|RAB23-related_Carpenter_syndrome|Carpenter_syndrome|not_provided": 1,
    "Carpenter_syndrome|RAB23-related_disorder": 4,
    "not_provided|Carpenter_syndrome|Inborn_genetic_diseases|RAB23-related_disorder|RAB23-related_Carpenter_syndrome": 1,
    "RAB23-related_disorder|Carpenter_syndrome|not_provided|RAB23-related_Carpenter_syndrome": 1,
    "RAB23-related_disorder|Inborn_genetic_diseases": 3,
    "RAB23-related_disorder|RAB23-related_Carpenter_syndrome|Carpenter_syndrome": 1,
    "not_specified|not_provided|RAB23-related_Carpenter_syndrome|Carpenter_syndrome": 1,
    "RAB23-related_Carpenter_syndrome|not_provided|RAB23-related_disorder|Carpenter_syndrome": 1,
    "Carpenter_syndrome|RAB23-related_Carpenter_syndrome": 1,
    "PHF3-related_disorder": 36,
    "PHF3-related_disorder|not_provided": 4,
    "not_provided|PHF3-related_disorder": 2,
    "not_specified|PHF3-related_disorder": 2,
    "Neurodevelopmental_delay|Intellectual_disability": 1,
    "PHF3-related_disorder|not_specified": 3,
    "not_specified|not_provided|Retinitis_pigmentosa_25": 2,
    "Retinitis_pigmentosa_25|not_provided": 220,
    "Retinitis_pigmentosa_25": 402,
    "Retinitis_pigmentosa_25|Retinal_dystrophy|not_provided": 11,
    "EYS-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 4,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_25|not_provided": 13,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 11,
    "not_provided|Retinitis_pigmentosa_25": 193,
    "Retinitis_pigmentosa_25|not_provided|Retinitis_pigmentosa": 13,
    "not_provided|Retinitis_pigmentosa_25|Inborn_genetic_diseases": 6,
    "Retinitis_Pigmentosa|_Recessive|not_provided|not_specified|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided": 14,
    "Retinal_dystrophy|Retinitis_pigmentosa_25|not_provided|Retinitis_pigmentosa": 4,
    "not_provided|Retinitis_pigmentosa_25|Retinal_dystrophy": 10,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|Retinal_dystrophy|EYS-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_25|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 2,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_25|not_provided": 13,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_25": 14,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa": 3,
    "Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_25|Retinal_dystrophy": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 5,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 3,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_25": 5,
    "not_specified|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25": 2,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 2,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 3,
    "EYS-related_disorder": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa|not_provided": 6,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_25|not_specified|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_25": 3,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 3,
    "not_provided|Retinitis_pigmentosa_25|Retinal_dystrophy|Retinitis_pigmentosa": 4,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 2,
    "Retinitis_pigmentosa_25|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_25": 9,
    "Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|EYS-related_disorder|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_specified": 2,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa": 5,
    "Visual_impairment|Retinal_dystrophy|Horizontal_nystagmus|Color_vision_defect|Dyschromatopsia|Abnormality_of_retinal_pigmentation|Electronegative_electroretinogram|Pigmentary_retinopathy|Cystoid_macular_edema|Astigmatism|Abnormal_electroretinogram|Retinitis_pigmentosa_25": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_25|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_specified|Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided": 3,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_25": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_25": 10,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 6,
    "Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 12,
    "Retinitis_pigmentosa_25|not_provided|Retinal_dystrophy": 8,
    "Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|not_provided|Inborn_genetic_diseases": 12,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 9,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25|EYS-related_disorder|Retinal_dystrophy": 1,
    "not_specified|Retinitis_pigmentosa_25|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_25|Retinal_dystrophy|not_provided": 3,
    "Retinitis_pigmentosa_25|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 3,
    "EYS-related_disorder|not_provided": 4,
    "Retinal_dystrophy|not_specified|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa": 2,
    "not_specified|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 1,
    "EYS-related_disorder|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|not_specified|not_provided": 2,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 15,
    "not_provided|EYS-related_disorder|Retinitis_pigmentosa_25|Retinal_dystrophy": 1,
    "not_provided|EYS-related_disorder": 5,
    "Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_25|EYS-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|EYS-related_disorder": 1,
    "Central_areolar_choroidal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa_25": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases|Retinitis_pigmentosa_25": 3,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25": 6,
    "Retinitis_pigmentosa_25|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 4,
    "not_provided|Retinitis_pigmentosa_25|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases": 2,
    "Retinitis_pigmentosa_25|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinal_dystrophy": 3,
    "EYS-related_disorder|Autosomal_recessive_retinitis_pigmentosa|not_provided": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25": 4,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|EYS-related_disorder|Retinitis_pigmentosa_25": 1,
    "See_cases|Retinitis_pigmentosa_25|not_provided": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided|Retinal_dystrophy": 2,
    "not_provided|Retinitis_pigmentosa_25|Inborn_genetic_diseases|Retinitis_pigmentosa|EYS-related_disorder": 1,
    "EYS-related_disorder|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_retinitis_pigmentosa": 4,
    "not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa|EYS-related_disorder": 2,
    "Retinitis_pigmentosa|not_specified|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "EYS-related_disorder|not_provided|Retinitis_pigmentosa_25": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25|EYS-related_disorder|Macular_dystrophy|Retinal_dystrophy": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_25|not_provided|EYS-related_disorder": 3,
    "not_specified|Retinitis_pigmentosa|not_provided|EYS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "not_provided|Retinitis_pigmentosa_25|not_specified": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25|EYS-related_disorder": 1,
    "Retinitis_pigmentosa_25|not_specified|Retinitis_pigmentosa|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25": 5,
    "Retinitis_pigmentosa_25|EYS-related_disorder|not_provided": 2,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 2,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|EYS-related_disorder": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|EYS-related_disorder|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|Autosomal_recessive_retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa_25|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|EYS-related_disorder|Retinitis_pigmentosa_25": 1,
    "not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 3,
    "EYS-related_disorder|Retinal_dystrophy|not_provided": 2,
    "EYS-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_25|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25|Retinal_dystrophy": 2,
    "Retinitis_punctata_albescens|Retinitis_pigmentosa_25|not_provided": 1,
    "Retinitis_pigmentosa_25|not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Visual_impairment|Retinal_detachment|Central_scotoma|Blurred_vision|Rod-cone_dystrophy": 1,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_25|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa_25|not_provided": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_25|not_specified": 1,
    "not_specified|Retinitis_pigmentosa_25|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_specified|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|EYS-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|not_specified|not_provided|Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|Optic_atrophy|not_provided|Retinitis_pigmentosa": 1,
    "EYS-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_25|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_25|Cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa_25|Retinal_dystrophy": 3,
    "Retinitis_pigmentosa_25|Optic_atrophy|Retinal_dystrophy|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|not_provided|Retinal_dystrophy|not_specified": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25|Inborn_genetic_diseases": 1,
    "EYS-related_disorder|Retinitis_pigmentosa_25|Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_25|not_specified|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_25|EYS-related_disorder": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases": 2,
    "EYS-related_disorder|Retinitis_pigmentosa_25|not_provided": 1,
    "EYS-related_disorder|Retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided|Retinal_dystrophy": 1,
    "EYS-related_disorder|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25": 1,
    "EYS-related_disorder|not_provided|Retinitis_pigmentosa": 2,
    "not_provided|EYS-related_retinopathy|Retinal_dystrophy|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_specified|not_provided|Cone-rod_dystrophy|Retinitis_pigmentosa_25": 1,
    "EYS-related_retinopathy|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_25|EYS-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_25|not_provided|Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25|EYS-related_disorder": 1,
    "not_provided|Retinitis_Pigmentosa|_Recessive|not_specified": 2,
    "not_provided|Abnormality_of_the_eye|Retinitis_pigmentosa_25": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_specified": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_25|EYS-related_disorder": 1,
    "Macular_dystrophy|Retinitis_pigmentosa_25|not_provided": 1,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|not_provided|Retinal_dystrophy|not_specified": 1,
    "EYS-related_disorder|Retinitis_pigmentosa_25": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 1,
    "Retinitis_pigmentosa|Stargardt_disease|Retinitis_pigmentosa_25|not_specified|not_provided": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_25": 1,
    "not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_25|Retinal_dystrophy|EYS-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_25|not_specified": 1,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "Macular_dystrophy|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_25": 1,
    "not_provided|Retinitis_pigmentosa_25|Inborn_genetic_diseases|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_25|Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_25": 1,
    "not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa|Retinal_dystrophy|not_specified": 1,
    "EYS-related_disorder|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25|EYS-related_disorder|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|EYS-related_disorder|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa|EYS-related_retinopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_25": 1,
    "Retinitis_pigmentosa_25|not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa_25|not_provided": 1,
    "EYS-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_25|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 2,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_25|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_25|Retinitis_pigmentosa": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_25|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_25|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_25|EYS-related_disorder|Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 1,
    "EYS-related_disorder|Retinitis_pigmentosa|not_provided": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF": 365,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 12,
    "not_specified|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 8,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_specified|not_provided": 2,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_provided": 3,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_specified": 6,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|Inborn_genetic_diseases|Cobalamin_C_disease": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 2,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 3,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblF|Inborn_genetic_diseases": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 1,
    "Inborn_genetic_diseases|LMBRD1-related_disorder|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Cobalamin_C_disease|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Donnai-Barrow_syndrome": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|Cobalamin_C_disease": 1,
    "LMBRD1-related_disorder|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|LMBRD1-related_disorder": 4,
    "Cobalamin_C_disease|not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblF": 1,
    "Inborn_genetic_diseases|Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_provided": 2,
    "not_provided|Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_specified": 1,
    "LMBRD1-related_disorder|Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_specified": 1,
    "Methylmalonic_aciduria_and_homocystinuria_type_cblF|not_provided|Inborn_genetic_diseases": 1,
    "Stickler_Syndrome|_Recessive|Multiple_Epiphyseal_Dysplasia|_Dominant": 2,
    "Stickler_Syndrome|_Recessive|Multiple_Epiphyseal_Dysplasia|_Dominant|not_provided": 1,
    "not_provided|COL9A1-related_disorder": 15,
    "Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4": 1,
    "not_provided|Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6": 2,
    "Retinal_dystrophy|Stickler_syndrome|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|COL9A1-related_disorder|Stickler_syndrome|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4|not_provided": 2,
    "COL9A1-related_disorder": 13,
    "not_provided|Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6|not_specified|Connective_tissue_disorder": 1,
    "Stickler_syndrome|_type_4|not_provided": 3,
    "COL9A1-related_disorder|not_provided": 14,
    "Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6|not_provided|Connective_tissue_disorder": 1,
    "Stickler_syndrome|_type_4": 6,
    "Inborn_genetic_diseases|not_provided|Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6": 1,
    "not_specified|Epiphyseal_dysplasia|_multiple|_6|not_provided": 5,
    "Inborn_genetic_diseases|Stickler_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|COL9A1-related_disorder|not_specified|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Optic_atrophy|Retinal_dystrophy|not_provided": 3,
    "not_provided|Stickler_syndrome|_type_4": 3,
    "Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6|not_provided": 2,
    "Epiphyseal_dysplasia|_multiple|_6|not_specified|not_provided": 4,
    "not_provided|Marfan_syndrome": 42,
    "Inborn_genetic_diseases|Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4|not_provided": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_6|not_specified": 1,
    "not_provided|Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6|Retinal_dystrophy": 1,
    "Stickler_syndrome|_type_4|not_provided|Connective_tissue_disorder": 1,
    "Hereditary_disease": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Epiphyseal_dysplasia|_multiple|_6": 1,
    "Multiple_Epiphyseal_Dysplasia|_Dominant|not_provided|Stickler_Syndrome|_Recessive": 1,
    "not_provided|not_specified|Epiphyseal_dysplasia|_multiple|_6": 1,
    "Stickler_syndrome|_type_4|Inborn_genetic_diseases|not_provided": 1,
    "COL9A1-related_disorder|not_specified|not_provided": 4,
    "Epiphyseal_dysplasia|_multiple|_6": 3,
    "not_provided|Stickler_syndrome|_type_4|COL9A1-related_disorder|Connective_tissue_disorder|Hearing_impairment|not_specified": 1,
    "Stickler_syndrome|_type_4|See_cases": 1,
    "Epiphyseal_dysplasia|_multiple|_6|not_provided": 1,
    "COL9A1-related_disorder|not_provided|Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6": 1,
    "Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6|not_provided|COL9A1-related_disorder": 1,
    "not_specified|not_provided|COL9A1-related_disorder": 1,
    "not_provided|not_specified|COL9A1-related_disorder": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4": 2,
    "COL9A1-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4": 1,
    "Stickler_syndrome|_type_4|Epiphyseal_dysplasia|_multiple|_6|not_specified|not_provided|COL9A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|COL9A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_6|Stickler_syndrome|_type_4|not_specified": 1,
    "Histiocytoid_cardiomyopathy": 1,
    "Cone-rod_dystrophy_7": 63,
    "not_provided|Cone-rod_dystrophy_7": 28,
    "Cone-Rod_Dystrophy|_Dominant": 30,
    "Cone-rod_dystrophy_7|not_provided": 15,
    "RIMS1-related_disorder|not_provided|not_specified|Cone-rod_dystrophy_7": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_7": 3,
    "RIMS1-related_disorder": 5,
    "not_provided|not_specified|Cone-rod_dystrophy_7": 3,
    "not_specified|Cone-rod_dystrophy_7|not_provided": 2,
    "not_specified|not_provided|Cone-rod_dystrophy_7": 10,
    "not_provided|RIMS1-related_disorder|Cone-rod_dystrophy_7": 1,
    "not_provided|Cone-rod_dystrophy_7|not_specified": 2,
    "RIMS1-related_disorder|not_provided": 4,
    "Cone-rod_dystrophy_7|not_specified|not_provided": 4,
    "Retinal_dystrophy|not_specified|not_provided|Cone-rod_dystrophy_7": 1,
    "Cone-rod_dystrophy_7|not_provided|not_specified": 1,
    "not_specified|not_provided|Cone-Rod_Dystrophy|_Dominant": 1,
    "not_provided|RIMS1-related_disorder": 7,
    "RIMS1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_7|Retinal_dystrophy": 1,
    "RIMS1-related_disorder|not_provided|Cone-rod_dystrophy_7": 3,
    "Cone-rod_dystrophy_7|not_provided|Retinal_dystrophy": 2,
    "not_provided|Leber_congenital_amaurosis|Cone-rod_dystrophy_7": 1,
    "Ornithine_aminotransferase_deficiency|not_provided": 8,
    "not_provided|Cone-rod_dystrophy_7|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_7": 1,
    "not_provided|RIMS1-related_disorder|not_specified": 1,
    "Cone-Rod_Dystrophy|_Dominant|not_provided": 6,
    "not_specified|not_provided|Cone-rod_dystrophy_7|RIMS1-related_disorder": 1,
    "Cone-Rod_Dystrophy|_Dominant|not_specified|not_provided": 1,
    "not_provided|Cone-Rod_Dystrophy|_Dominant": 7,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_46|not_provided|Cleft_palate|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_46": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|KCNQ5-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_46": 49,
    "KCNQ5-related_disorder|not_provided": 12,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_46": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_46": 5,
    "KCNQ5-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_46": 1,
    "KCNQ5-related_disorder": 7,
    "not_provided|KCNQ5-related_disorder": 8,
    "Inborn_genetic_diseases|KCNQ5-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_46|not_provided": 9,
    "Global_developmental_delay|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_46|Inborn_genetic_diseases|not_provided": 1,
    "KCNQ5-related_disorder|Intellectual_disability|_autosomal_dominant_46|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_ataxia|not_provided|KCNQ5-related_disorder": 1,
    "Hydatidiform_mole|_recurrent|_2": 4,
    "Hydatidiform_mole|_recurrent|_2|KHDC3L-related_condition": 1,
    "Hydatidiform_mole": 5,
    "Inherited_oocyte_maturation_defect": 7,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 518,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 6,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|Inborn_genetic_diseases": 20,
    "Inborn_genetic_diseases|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 31,
    "Inborn_genetic_diseases|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_provided": 2,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_specified": 5,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_provided": 14,
    "MTO1-related_disorder": 5,
    "not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 19,
    "not_specified|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|MTO1-related_disorder": 1,
    "not_specified|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 4,
    "MTO1-related_disorder|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 5,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|MTO1-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 4,
    "not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|MTO1-related_disorder": 1,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|MTO1-related_disorder": 3,
    "not_specified|not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 4,
    "not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|Inborn_genetic_diseases": 3,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 1,
    "not_provided|MTO1-related_disorder": 3,
    "Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_specified": 2,
    "Hereditary_motor_neuron_disease": 2,
    "Mitochondrial_oxidative_phosphorylation_disorder|not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|Global_developmental_delay": 1,
    "not_provided|not_specified|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 1,
    "MTO1-related_disorder|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|not_provided|not_specified": 1,
    "not_provided|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency|Abnormal_brain_morphology": 1,
    "not_provided|MTO1-related_disorder|Mitochondrial_hypertrophic_cardiomyopathy_with_lactic_acidosis_due_to_MTO1_deficiency": 1,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type": 42,
    "Salla_disease": 414,
    "Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 71,
    "Sialic_acid_storage_disease|_severe_infantile_type|not_provided|Salla_disease": 3,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|not_provided": 6,
    "not_provided|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type": 4,
    "Salla_disease|Inborn_genetic_diseases": 8,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|SLC17A5-related_disorder": 2,
    "Inborn_genetic_diseases|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "Inborn_genetic_diseases|Salla_disease": 11,
    "Salla_disease|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|not_specified|Salla_disease": 1,
    "SLC17A5-related_disorder|not_specified|not_provided|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease|Inborn_genetic_diseases": 2,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|Inborn_genetic_diseases|not_provided": 1,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|Inborn_genetic_diseases": 3,
    "Sialic_acid_storage_disease|_severe_infantile_type": 4,
    "Free_sialic_acid_storage_disease": 1,
    "not_provided|Salla_disease": 4,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|not_provided|Focal_segmental_glomerulosclerosis|Inborn_genetic_diseases": 1,
    "Salla_disease|not_specified|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "Inborn_genetic_diseases|Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 2,
    "SLC17A5-related_disorder|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|not_provided": 1,
    "not_provided|not_specified|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "Salla_disease|SLC17A5-related_disorder": 2,
    "Salla_disease|Inborn_genetic_diseases|Sialic_acid_storage_disease|_severe_infantile_type": 2,
    "Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease|not_provided": 7,
    "not_provided|Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 7,
    "not_provided|SLC17A5-related_disorder|Inborn_genetic_diseases|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease|not_provided|not_specified": 1,
    "Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease|not_provided|Inborn_genetic_diseases|Familial_hypokalemia-hypomagnesemia|Enhanced_S-cone_syndrome": 1,
    "not_provided|not_specified|Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 1,
    "Intermediate_severe_Salla_disease|not_provided|Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 1,
    "Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease|SLC17A5-related_disorder": 1,
    "not_specified|not_provided|Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 1,
    "Inborn_genetic_diseases|not_provided|Sialic_acid_storage_disease|_severe_infantile_type|Salla_disease": 1,
    "Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|Inborn_genetic_diseases|not_specified": 1,
    "Salla_disease|not_provided|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "not_specified|Salla_disease|Sialic_acid_storage_disease|_severe_infantile_type|not_provided": 1,
    "not_provided|Salla_disease|SLC17A5-related_disorder|Sialic_acid_storage_disease|_severe_infantile_type": 1,
    "Inborn_genetic_diseases|SLC17A5-related_disorder|Salla_disease": 1,
    "Inborn_genetic_diseases|Salla_disease|SLC17A5-related_disorder|not_provided": 1,
    "Multiple_sclerosis|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 12,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_provided": 25,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1878,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 354,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified|not_provided": 14,
    "not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases": 6,
    "not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 160,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided": 156,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|Inborn_genetic_diseases": 15,
    "Abnormality_of_connective_tissue": 3,
    "Bethlem_myopathy_2": 37,
    "not_specified|not_provided|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 37,
    "COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 7,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 3,
    "See_cases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided": 1,
    "COL12A1-related_disorder|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 5,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|COL12A1-related_disorder|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases": 40,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|COL12A1-related_disorder|not_specified|not_provided": 2,
    "not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 21,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided": 35,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified": 14,
    "not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided": 18,
    "COL12A1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|not_specified": 8,
    "COL12A1-related_disorder": 13,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|COL12A1-related_disorder|not_provided": 6,
    "not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_specified": 2,
    "Inborn_genetic_diseases|Global_developmental_delay": 1,
    "not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases|not_provided": 1,
    "COL12A1-related_disorder|not_provided|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 41,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|Inborn_genetic_diseases": 11,
    "Ullrich_congenital_muscular_dystrophy_2": 9,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 1,
    "not_provided|Bethlem_myopathy_2": 2,
    "not_provided|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 15,
    "not_provided|COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 5,
    "not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|See_cases|not_provided": 1,
    "COL12A1-related_disorder|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_provided": 2,
    "not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified": 8,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified|not_provided": 1,
    "not_specified|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|COL12A1-related_disorder": 1,
    "Bethlem_myopathy|Ullrich_congenital_muscular_dystrophy|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Bethlem_myopathy_2|not_provided": 2,
    "Inborn_genetic_diseases|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 6,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|COL12A1-related_disorder|not_provided": 1,
    "not_provided|COL12A1-related_disorder|not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|COL12A1-related_disorder": 1,
    "COL12A1-related_disorder|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified": 1,
    "Ehlers-Danlos_syndrome|not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_provided|COL12A1-related_disorder": 2,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases|not_provided": 14,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_specified|not_provided": 2,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|COL12A1-related_disorder|not_specified|not_provided": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_provided|not_specified": 2,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|COL12A1-related_disorder": 7,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 8,
    "not_provided|COL12A1-related_disorder": 2,
    "not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases|Myopathic_Ehlers-Danlos_syndrome": 1,
    "COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided": 10,
    "not_specified|not_provided|COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 2,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|Cataract_16_multiple_types": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|COL12A1-related_disorder": 2,
    "not_provided|COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases|not_provided|not_specified|COL12A1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "not_specified|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_provided": 3,
    "Ullrich_congenital_muscular_dystrophy|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|COL12A1-related_disorder": 1,
    "not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|COL12A1-related_disorder": 2,
    "not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|COL12A1-related_disorder": 1,
    "not_provided|COL12A1-related_disorder|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 2,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_specified|COL12A1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Bethlem_myopathy_2|not_provided|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Ullrich_congenital_muscular_dystrophy|Bethlem_myopathy_2|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Bethlem_myopathy|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|COL12A1-related_disorder": 1,
    "COL12A1-related_disorder|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 2,
    "Bethlem_myopathy_2|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|not_provided": 1,
    "COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified|not_provided": 2,
    "COL12A1-related_disorder|not_provided": 1,
    "COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy|not_provided|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "COL12A1-related_disorder|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Inborn_genetic_diseases|COL12A1-related_disorder|not_specified|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Ullrich_congenital_muscular_dystrophy|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "not_provided|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|Inborn_genetic_diseases": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "EMG_abnormality|EMG:_myotonic_runs": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|COL12A1-related_disorder|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Myopathic_Ehlers-Danlos_syndrome": 1,
    "not_provided|not_specified|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 1,
    "not_provided|Inborn_genetic_diseases|Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Bethlem_myopathy_2|Ullrich_congenital_muscular_dystrophy_2|Ullrich_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|not_specified|Bartter_disease_type_4B|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2": 1,
    "Bethlem_myopathy_2|Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2": 1,
    "Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_specified|not_provided|COL12A1-related_disorder": 1,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_2|Bethlem_myopathy_2|not_provided|not_specified": 1,
    "Neuromuscular_disorder|_congenital|_with_dysmorphic_facies": 5,
    "Abnormality_of_neuronal_migration|not_specified": 1,
    "Epicanthus|Delayed_speech_and_language_development|Synophrys|High|_narrow_palate": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|Hearing_loss|_autosomal_recessive": 5,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 11,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 15,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 84,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 25,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37": 13,
    "MYO6-related_disorder": 17,
    "not_specified|not_provided|MYO6-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|not_provided": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_specified|MYO6-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22": 18,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_specified|not_provided|Rare_genetic_deafness": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Meniere_disease|not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 3,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|Inborn_genetic_diseases": 1,
    "not_provided|MYO6-related_disorder|Inborn_genetic_diseases": 1,
    "MYO6-related_disorder|not_provided": 4,
    "Rare_genetic_deafness|Progressive_sensorineural_hearing_loss-hypertrophic_cardiomyopathy_syndrome|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|Rare_genetic_deafness": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided|Hearing_impairment": 2,
    "MYO6-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "not_provided|Meniere_disease|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_22": 2,
    "not_provided|MYO6-related_disorder|not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_specified|not_provided": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_specified": 6,
    "not_specified|not_provided|Nonsyndromic_Hearing_Loss|_Dominant|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|MYO6-related_disorder": 1,
    "not_specified|Nonsyndromic_Hearing_Loss|_Dominant|Hearing_loss|_autosomal_recessive|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|MYO6-related_disorder": 1,
    "MYO6-related_disorder|not_provided|Obesity|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Rare_genetic_deafness|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Nonsyndromic_genetic_hearing_loss|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Essential_tremor|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|MYO6-related_disorder|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|not_specified|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Inborn_genetic_diseases": 1,
    "MYO6-related_disorder|Nonsyndromic_genetic_hearing_loss|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_37|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22": 3,
    "not_provided|Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22|not_specified|Infertility_disorder|Male_infertility": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_37|Autosomal_dominant_nonsyndromic_hearing_loss_22": 2,
    "MYO6-related_disorder|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "MYO6-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_37": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_22": 1,
    "not_provided|MYO6-related_disorder": 1,
    "Hearing_loss|_autosomal_recessive|Nonsyndromic_Hearing_Loss|_Dominant": 8,
    "not_provided|Hearing_loss|_autosomal_recessive|Nonsyndromic_Hearing_Loss|_Dominant": 2,
    "Hearing_loss|_autosomal_recessive|not_provided|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "Vitelliform_macular_dystrophy_4": 6,
    "not_specified|not_provided|IMPG1-related_disorder": 1,
    "Vitelliform_macular_dystrophy_4|Retinal_dystrophy|not_provided": 2,
    "IMPG1-related_disorder|not_provided": 7,
    "Retinal_dystrophy|Vitelliform_macular_dystrophy_4|not_provided": 1,
    "IMPG1-related_disorder": 3,
    "not_provided|Vitelliform_macular_dystrophy_4": 1,
    "not_provided|Benign_concentric_annular_macular_dystrophy|Retinitis_pigmentosa": 1,
    "Benign_concentric_annular_macular_dystrophy|not_provided": 2,
    "Benign_concentric_annular_macular_dystrophy|Vitelliform_macular_dystrophy_4|not_provided": 1,
    "Vitelliform_macular_dystrophy_4|Retinitis_pigmentosa|not_provided|Benign_concentric_annular_macular_dystrophy": 1,
    "Vitelliform_macular_dystrophy_4|Vitelliform_macular_dystrophy_1|not_provided": 1,
    "Retinal_dystrophy|Benign_concentric_annular_macular_dystrophy|Vitelliform_macular_dystrophy_4|not_provided": 1,
    "not_provided|IMPG1-related_disorder": 6,
    "IMPG1-related_disorder|Vitelliform_macular_dystrophy_4|not_provided": 1,
    "not_provided|Vitelliform_macular_dystrophy_4|Benign_concentric_annular_macular_dystrophy": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy": 2,
    "Benign_concentric_annular_macular_dystrophy|Vitelliform_macular_dystrophy_4|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Vitelliform_macular_dystrophy_5|not_provided": 1,
    "Benign_concentric_annular_macular_dystrophy": 1,
    "Retinal_dystrophy|Vitelliform_macular_dystrophy_4": 1,
    "not_provided|Benign_concentric_annular_macular_dystrophy|Vitelliform_macular_dystrophy_4|Retinal_dystrophy": 1,
    "not_provided|IMPG1-related_disorder|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Incidental_Discovery": 1,
    "not_provided|Isolated_macular_dystrophy|Retinal_dystrophy": 1,
    "Vitelliform_macular_dystrophy_4|not_specified|not_provided": 1,
    "PHIP-related_disorder": 166,
    "not_provided|PHIP-related_disorder": 48,
    "PHIP-related_disorder|not_provided": 65,
    "PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 109,
    "PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "PHIP-related_disorder|Inborn_genetic_diseases": 3,
    "PHIP-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|PHIP-related_disorder": 6,
    "Inborn_genetic_diseases|PHIP-related_disorder": 7,
    "PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided": 13,
    "PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 3,
    "PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 19,
    "not_provided|not_specified|Inborn_genetic_diseases|PHIP-related_disorder": 1,
    "PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|PHIP-related_disorder": 1,
    "not_specified|PHIP-related_disorder|not_provided": 1,
    "not_provided|PHIP-related_disorder|Inborn_genetic_diseases": 1,
    "See_cases|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided": 1,
    "PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided": 6,
    "PHIP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Rare_genetic_intellectual_disability|not_provided|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|PHIP-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PHIP-related_disorder": 1,
    "Inborn_genetic_diseases|PHIP-related_disorder|not_provided": 1,
    "PHIP-related_disorder|not_specified|not_provided": 3,
    "PHIP-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|PHIP-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 1,
    "not_provided|PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 1,
    "not_provided|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 1,
    "Inborn_genetic_diseases|PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 1,
    "not_specified|PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided": 1,
    "not_provided|See_cases|PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome": 1,
    "Exercise_intolerance|_riboflavin-responsive": 1,
    "Inborn_genetic_diseases|PHIP-related_disorder|Intellectual_disability|_X-linked_102|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided": 1,
    "PHIP-related_disorder|PHIP-related_behavioral_problems-intellectual_disability-obesity-dysmorphic_features_syndrome|not_provided|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_specified|not_provided|PHIP-related_disorder": 1,
    "not_provided|Leber_congenital_amaurosis_5": 58,
    "Leber_congenital_amaurosis_5|not_provided": 37,
    "Leber_congenital_amaurosis_5|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_5": 3,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_5|not_provided": 3,
    "not_provided|not_specified|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_5": 1,
    "Leber_congenital_amaurosis|Early-onset_retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 2,
    "not_provided|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "LCA5-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis_5": 10,
    "Leber_congenital_amaurosis_5|Retinal_dystrophy": 1,
    "not_provided|Leber_congenital_amaurosis_5|Inborn_genetic_diseases": 3,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis_5": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_5|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Leber_congenital_amaurosis_5|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_1|not_provided|Leber_congenital_amaurosis_5": 1,
    "LCA5-related_disorder|Leber_congenital_amaurosis_5|Leber_congenital_amaurosis|not_provided": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|not_provided|Leber_congenital_amaurosis_5|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_5": 1,
    "LCA5-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_5|Polycystic_liver_disease_2|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_5|Leber_congenital_amaurosis": 3,
    "not_provided|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_5|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_5|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Leber_congenital_amaurosis_5": 3,
    "not_provided|Leber_congenital_amaurosis|Inborn_genetic_diseases|LCA5-related_disorder": 1,
    "not_provided|LCA5-related_disorder": 1,
    "not_specified|Leber_congenital_amaurosis_5|Retinitis_pigmentosa|not_provided": 1,
    "Leber_congenital_amaurosis_5|not_provided|Leber_congenital_amaurosis|LCA5-related_disorder": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Inborn_genetic_diseases|LCA5-related_disorder": 1,
    "Leber_congenital_amaurosis_5|LCA5-related_retinopathy|not_provided": 1,
    "Leber_congenital_amaurosis_5|not_provided|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis|LCA5-related_disorder|not_provided": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis_5": 1,
    "not_provided|not_specified|Leber_congenital_amaurosis_5": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_5": 1,
    "Stargardt_Disease|_Dominant": 8,
    "Spinocerebellar_ataxia_type_34|not_specified|not_provided|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|Stargardt_disease_3": 1,
    "Spinocerebellar_ataxia_type_34|Stargardt_disease_3|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Stargardt_disease_3": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_34": 1,
    "Spinocerebellar_ataxia_type_34|not_provided": 1,
    "Stargardt_disease_3|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_type_34|not_provided|ELOVL4-related_disorder": 1,
    "Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome": 2,
    "not_provided|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome": 1,
    "ELOVL4-related_disorder|not_provided": 1,
    "Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|not_provided": 1,
    "ELOVL4-related_ataxia": 1,
    "Spinocerebellar_ataxia_type_34|Stargardt_disease_3|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|not_provided": 1,
    "ELOVL4-related_disorder|Spinocerebellar_ataxia_type_34|Stargardt_disease_3|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome": 1,
    "not_provided|ELOVL4-related_disorder": 1,
    "ELOVL4-related_disorder|Spinocerebellar_ataxia_type_34|Stargardt_disease_3|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Stargardt_disease_3": 1,
    "Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|ELOVL4-related_disorder": 1,
    "not_provided|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|Spinocerebellar_ataxia_type_34|Stargardt_disease_3": 2,
    "Stargardt_disease_3|not_provided|ELOVL4-related_disorder": 1,
    "not_provided|Spinocerebellar_ataxia_type_34": 1,
    "Spinocerebellar_ataxia_type_34|Stargardt_disease|Congenital_ichthyosis-intellectual_disability-spastic_quadriplegia_syndrome|not_provided": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A": 5,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_1B": 2,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1B": 20,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease": 2,
    "Maple_syrup_urine_disease_type_1B": 37,
    "not_provided|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease|BCKDHB-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease": 18,
    "Maple_syrup_urine_disease_type_1B|not_provided|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|not_provided": 2,
    "not_provided|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1B": 2,
    "not_provided|Maple_syrup_urine_disease_type_1B|not_specified|Maple_syrup_urine_disease": 1,
    "not_specified|Maple_syrup_urine_disease|not_provided|Maple_syrup_urine_disease_type_1B": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease": 1,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1B|not_specified": 1,
    "not_provided|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 8,
    "Maple_syrup_urine_disease|not_specified|Maple_syrup_urine_disease_type_1B": 1,
    "Maple_syrup_urine_disease_type_1B|not_provided": 2,
    "Maple_syrup_urine_disease_type_1B|Inborn_genetic_diseases": 1,
    "not_specified|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A": 1,
    "not_provided|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease": 4,
    "Inborn_genetic_diseases|BCKDHB-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1B": 4,
    "Maple_syrup_urine_disease|not_specified|not_provided": 3,
    "BCKDHB-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 6,
    "Maple_syrup_urine_disease|BCKDHB-related_disorder|not_provided|Abnormality_of_metabolism/homeostasis|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_1B": 1,
    "Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease|Inborn_genetic_diseases": 1,
    "not_specified|Maple_syrup_urine_disease_type_1B|not_provided": 1,
    "Maple_syrup_urine_disease_type_1B|not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 2,
    "not_provided|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A": 1,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A|not_provided|Maple_syrup_urine_disease": 1,
    "Inborn_genetic_diseases|BCKDHB-related_disorder|not_provided|Maple_syrup_urine_disease": 1,
    "Inborn_genetic_diseases|not_provided|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "not_provided|Maple_syrup_urine_disease_type_1B": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1B|not_provided": 1,
    "Maple_syrup_urine_disease_type_1B|not_specified": 2,
    "Maple_syrup_urine_disease|BCKDHB-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|BCKDHB-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1A|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease|not_provided|BCKDHB-related_disorder|Inborn_genetic_diseases": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease|not_provided": 1,
    "BCKDHB-related_disorder|not_provided|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "not_provided|Maple_syrup_urine_disease_type_1A": 2,
    "not_specified|Maple_syrup_urine_disease_type_1B|not_provided|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_1A|BCKDHB-related_disorder|not_provided|Maple_syrup_urine_disease": 1,
    "not_specified|Maple_syrup_urine_disease_type_1B|Maple_syrup_urine_disease_type_1A|not_provided|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|BCKDHB-related_disorder|Maple_syrup_urine_disease_type_1B": 1,
    "Maple_syrup_urine_disease_type_1B|not_provided|Maple_syrup_urine_disease_type_1A": 1,
    "TENT5A-related_disorder|not_provided": 2,
    "Osteogenesis_imperfecta|_type_18": 6,
    "Osteogenesis_imperfecta|_type_18|not_specified": 1,
    "not_provided|Osteogenesis_imperfecta|_type_18|not_specified": 1,
    "not_provided|TENT5A-related_disorder": 2,
    "Osteogenesis_imperfecta|_type_18|not_specified|not_provided": 1,
    "TENT5A-related_disorder|not_specified": 1,
    "TENT5A-related_disorder": 1,
    "PGM3-related_disorder": 1,
    "Immunodeficiency_23": 464,
    "not_specified|Immunodeficiency_23": 2,
    "Inborn_genetic_diseases|Immunodeficiency_23": 12,
    "not_provided|Immunodeficiency_23": 5,
    "Inborn_genetic_diseases|Immunodeficiency_23|not_provided": 1,
    "Hyper-IgE_syndrome|Immunodeficiency_23": 2,
    "not_provided|Immunodeficiency_23|Severe_combined_immunodeficiency_disease": 2,
    "Immunodeficiency_23|Inborn_genetic_diseases": 8,
    "PGM3-related_disorder|Immunodeficiency_23|not_provided": 1,
    "Immunodeficiency_23|not_provided": 7,
    "not_provided|Immunodeficiency_23|Inborn_genetic_diseases": 1,
    "PGM3-related_disorder|Immunodeficiency_23": 5,
    "PGM3-related_disorder|Severe_combined_immunodeficiency_disease|Immunodeficiency_23": 1,
    "Inborn_genetic_diseases|Immunodeficiency_23|not_specified|PGM3-related_disorder": 1,
    "not_specified|not_provided|Immunodeficiency_23": 2,
    "Hyper-IgE_syndrome|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|Immunodeficiency_23|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency_23|Severe_combined_immunodeficiency_disease": 1,
    "not_specified|PGM3-related_disorder|Immunodeficiency_23": 1,
    "Immunodeficiency_23|PGM3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency_23|not_specified": 1,
    "Immunodeficiency_23|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency_disease|not_provided|Immunodeficiency_23": 1,
    "not_provided|PGM3-related_disorder|Immunodeficiency_23": 1,
    "Spondylocostal_dysostosis_6|_autosomal_recessive|not_provided": 1,
    "RIPPLY2-related_disorder|Spondylocostal_dysostosis_6|_autosomal_recessive|not_provided": 1,
    "RIPPLY2-related_disorder|not_provided": 1,
    "Spondylocostal_dysostosis_6|_autosomal_recessive|not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "RIPPLY2-related_disorder|Spondylocostal_dysostosis_6|_autosomal_recessive|not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "Klippel-Feil_syndrome_2|_autosomal_recessive|not_provided": 2,
    "MRAP2-related_disorder": 56,
    "MRAP2-related_disorder|not_provided": 7,
    "not_specified|MRAP2-related_disorder": 2,
    "Body_mass_index_quantitative_trait_locus_18": 1,
    "not_provided|MRAP2-related_disorder": 3,
    "Hypoplasia_of_anterior_or_entire_pituitary_gland_(frequent)": 1,
    "MRAP2-related_disorder|not_provided|not_specified": 1,
    "not_provided|Body_mass_index_quantitative_trait_locus_18": 1,
    "MRAP2-related_disorder|not_specified": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_2": 11,
    "TBX18-related_disorder": 9,
    "Incidental_Discovery|Congenital_anomalies_of_kidney_and_urinary_tract_2": 1,
    "Proteinuria|Inborn_genetic_diseases": 1,
    "TBX18-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_2": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|TBX18-related_disorder": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_2|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_2": 2,
    "not_provided|TBX18-related_disorder": 3,
    "Chronic_kidney_disease|TBX18-related_disorder|not_provided": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_anomalies_of_kidney_and_urinary_tract_2": 1,
    "not_provided|Inborn_genetic_diseases|TBX18-related_disorder": 1,
    "TBX18-related_disorder|Inborn_genetic_diseases": 1,
    "NT5E-related_disorder": 10,
    "NT5E-related_disorder|not_provided": 2,
    "Hereditary_arterial_and_articular_multiple_calcification_syndrome": 3,
    "NT5E-related_disorder|not_provided|Hereditary_arterial_and_articular_multiple_calcification_syndrome": 1,
    "Hereditary_arterial_and_articular_multiple_calcification_syndrome|not_specified": 2,
    "not_provided|NT5E-related_disorder": 1,
    "NT5E-related_disorder|Hereditary_arterial_and_articular_multiple_calcification_syndrome": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_20|not_provided": 4,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_20": 5,
    "Autosomal_recessive_spinocerebellar_ataxia_20": 31,
    "Autosomal_recessive_spinocerebellar_ataxia_20|SNX14-related_disorder": 1,
    "SNX14-related_disorder|not_provided": 7,
    "SNX14-related_disorder": 4,
    "not_provided|SNX14-related_disorder": 2,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_20|Spinocerebellar_atrophy": 1,
    "not_specified|not_provided|SNX14-related_disorder": 1,
    "Cerebellar_ataxia|Global_developmental_delay": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_20": 3,
    "Autosomal_recessive_spinocerebellar_ataxia_20|not_provided|SNX14-related_disorder": 1,
    "SYNCRIP-related_disorder": 8,
    "SYNCRIP-related_Intellectual_Disability": 1,
    "not_provided|SYNCRIP-related_disorder": 1,
    "SYNCRIP-related_neurodevelopmental_disorder": 2,
    "SYNCRIP-associated_neurodevelopmental_disorder": 1,
    "Head_and_neck_cancer": 4,
    "Intellectual_developmental_disorder|_autosomal_dominant_64": 81,
    "ZNF292-related_disorder": 44,
    "Neurodevelopmental_disorder|Intellectual_disability|Intellectual_developmental_disorder|_autosomal_dominant_64": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_dominant_64": 6,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|not_provided": 3,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder|_autosomal_dominant_64": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|Neurodevelopmental_disorder|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_64": 4,
    "ZNF292-related_disorder|not_provided|Neurodevelopmental_disorder": 1,
    "not_provided|ZNF292-related_disorder": 6,
    "not_provided|Complex_neurodevelopmental_disorder|ZNF292-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|Neurodevelopmental_disorder": 2,
    "not_provided|Inborn_genetic_diseases|ZNF292-related_disorder": 3,
    "Intellectual_disability|Neurodevelopmental_disorder": 1,
    "Intellectual_disability|Intellectual_developmental_disorder|_autosomal_dominant_64|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|ZNF292-related_disorder": 5,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|Motor_delay": 1,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder|_autosomal_dominant_64|Microcephaly|Intellectual_disability|_mild|Short_stature|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_dominant_64|Neurodevelopmental_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|Inborn_genetic_diseases": 3,
    "Intellectual_developmental_disorder|_autosomal_dominant_64|ZNF292-related_disorder": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|Intellectual_developmental_disorder|_autosomal_dominant_64|Inborn_genetic_diseases": 1,
    "ZNF292-related_disorder|not_provided": 4,
    "ZNF292-related_disorder|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|ZNF292-related_disorder|not_provided": 1,
    "not_provided|ZNF292-related_disorder|Intellectual_disability|Intellectual_developmental_disorder|_autosomal_dominant_64": 1,
    "Neurodevelopmental_disorder|Intellectual_disability|Intellectual_developmental_disorder|_autosomal_dominant_64|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder|_autosomal_dominant_64|not_provided": 1,
    "ZNF292-related_neurodevelopmental_condition|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|ZNF292-related_disorder": 1,
    "Neurodevelopmental_disorder|Intellectual_disability": 1,
    "Autism|Intellectual_developmental_disorder|_autosomal_dominant_64": 1,
    "Abnormal_sperm_tail_morphology": 1,
    "SLC35A1-congenital_disorder_of_glycosylation|not_specified": 2,
    "SLC35A1-congenital_disorder_of_glycosylation": 40,
    "not_specified|not_provided|SLC35A1-congenital_disorder_of_glycosylation": 1,
    "SLC35A1-related_disorder|not_specified|not_provided|SLC35A1-congenital_disorder_of_glycosylation": 2,
    "SLC35A1-related_disorder": 2,
    "Inborn_genetic_diseases|SLC35A1-congenital_disorder_of_glycosylation": 3,
    "SLC35A1-congenital_disorder_of_glycosylation|not_provided": 2,
    "not_provided|SLC35A1-related_disorder": 1,
    "SLC35A1-congenital_disorder_of_glycosylation|SLC35A1-related_disorder|not_provided": 1,
    "SLC35A1-related_disorder|SLC35A1-congenital_disorder_of_glycosylation|not_specified": 1,
    "not_provided|CONGENITAL_DISORDER_OF_GLYCOSYLATION|_TYPE_IIf|_MODIFIER_OF": 1,
    "SLC35A1-congenital_disorder_of_glycosylation|not_specified|not_provided|Pontoneocerebellar_hypoplasia|Congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|not_provided|SLC35A1-congenital_disorder_of_glycosylation": 1,
    "SLC35A1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Congenital_disorder_of_glycosylation|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "Pontoneocerebellar_hypoplasia|Congenital_disorder_of_glycosylation": 3,
    "Pontoneocerebellar_hypoplasia|Congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|RARS2-related_disorder": 1,
    "RARS2-related_disorder": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_6": 4,
    "Pontocerebellar_hypoplasia_type_6|Inborn_genetic_diseases|not_provided": 2,
    "Pontocerebellar_hypoplasia_type_6|Pontoneocerebellar_hypoplasia|Congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_6": 71,
    "Pontocerebellar_hypoplasia_type_6|not_provided": 51,
    "Pontocerebellar_hypoplasia_type_6": 110,
    "Pontocerebellar_hypoplasia_type_6|not_specified|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_6|Inborn_genetic_diseases": 4,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_6": 1,
    "Pontocerebellar_hypoplasia_type_6|RARS2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Pontocerebellar_hypoplasia_type_6": 3,
    "Pontoneocerebellar_hypoplasia|Inborn_genetic_diseases|not_provided": 1,
    "RARS2-related_disorder|not_specified|not_provided|Pontocerebellar_hypoplasia_type_6": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_6|Pontoneocerebellar_hypoplasia": 4,
    "Pontocerebellar_hypoplasia_type_6|not_provided|not_specified": 3,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_6|Inborn_genetic_diseases": 1,
    "Abnormal_brain_morphology|not_provided|RARS2-related_disorder|Inborn_genetic_diseases|Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_6": 1,
    "not_provided|RARS2-related_disorder|Pontocerebellar_hypoplasia_type_6": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_6": 6,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_6": 3,
    "RARS2-related_disorder|not_provided": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Pontocerebellar_hypoplasia_type_6": 2,
    "Pontocerebellar_hypoplasia_type_6|not_specified": 3,
    "Pontocerebellar_hypoplasia_type_6|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_6|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_6|RARS2-related_disorder": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Pontocerebellar_hypoplasia_type_6|Congenital_cerebellar_hypoplasia": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_6|not_provided": 2,
    "not_provided|Pontocerebellar_hypoplasia_type_6|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|not_specified|RARS2-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_6|Inborn_genetic_diseases": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_6|not_provided|RARS2-related_disorder": 1,
    "not_provided|Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_6": 1,
    "Pontocerebellar_hypoplasia_type_6|Pontoneocerebellar_hypoplasia": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_6": 1,
    "Pontocerebellar_hypoplasia_type_6|not_provided|Severe_intellectual_deficiency": 1,
    "not_specified|RARS2-related_disorder": 1,
    "not_provided|not_specified|Pontocerebellar_hypoplasia_type_6|RARS2-related_disorder": 1,
    "not_provided|Mitochondrial_disease|Pontocerebellar_hypoplasia_type_6": 1,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia_type_6": 2,
    "RARS2-related_disorder|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_6|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_6|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_6": 1,
    "Pontocerebellar_hypoplasia_type_6|RARS2-related_disorder|not_specified": 1,
    "ORC3-related_disorder": 2,
    "Spermatogenic_failure_85": 1,
    "CNR1-related_disorder": 3,
    "Hypomagnesemia_7|_renal|_with_or_without_dilated_cardiomyopathy": 4,
    "HYPOMAGNESEMIA_7|_RENAL|_WITH_DILATED_CARDIOMYOPATHY": 1,
    "not_provided|HYPOMAGNESEMIA_7|_RENAL|_WITH_DILATED_CARDIOMYOPATHY": 1,
    "HYPOMAGNESEMIA_7|_RENAL|_WITHOUT_DILATED_CARDIOMYOPATHY": 2,
    "RRAGD-related_disorder|Hypomagnesemia_7|_renal|_with_or_without_dilated_cardiomyopathy": 1,
    "ANKRD6-related_disorder": 11,
    "ANKRD6-related_disorder|not_provided": 1,
    "not_provided|MDN1-related_disorder": 5,
    "MDN1-related_disorder": 100,
    "MDN1-related_disorder|not_specified": 6,
    "not_specified|MDN1-related_disorder": 3,
    "MDN1-related_disorder|not_provided": 2,
    "BACH2-related_disorder": 5,
    "not_provided|Immunodeficiency_60": 3,
    "Immunodeficiency_60": 7,
    "Immunodeficiency_60|not_provided": 2,
    "BACH2-related_disorder|not_provided": 12,
    "not_specified|BACH2-related_disorder|not_provided": 2,
    "BACH2-related_disorder|not_specified|not_provided": 1,
    "not_provided|BACH2-related_disorder": 6,
    "Immunodeficiency_60|not_provided|not_specified": 1,
    "Immunodeficiency_60|not_specified|not_provided": 2,
    "not_provided|Immunodeficiency_60|not_specified": 2,
    "Autosomal_recessive_congenital_ichthyosis|not_provided|Immunodeficiency_60": 1,
    "BACH2-related_disorder|Immunodeficiency_60|not_provided": 1,
    "Frontometaphyseal_dysplasia_2|not_provided": 1,
    "not_provided|MAP3K7-related_disorder": 3,
    "MAP3K7-related_disorder": 4,
    "Frontometaphyseal_dysplasia_2": 5,
    "Inborn_genetic_diseases|Frontometaphyseal_dysplasia_2": 1,
    "MAP3K7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "MAP3K7-related_disorder|not_provided": 1,
    "Frontometaphyseal_dysplasia_2|Cardiospondylocarpofacial_syndrome": 3,
    "Cardiospondylocarpofacial_syndrome": 11,
    "Cardiospondylocarpofacial_syndrome|Frontometaphyseal_dysplasia_2": 1,
    "not_provided|Delayed_skeletal_maturation": 1,
    "not_provided|Cardiospondylocarpofacial_syndrome": 3,
    "Cardiospondylocarpofacial_syndrome|not_provided": 1,
    "Letrozole_response": 2,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_15": 3,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 2,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_15|Mitochondrial_complex_I_deficiency": 1,
    "NDUFAF4-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_15": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_15|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_15": 1,
    "POU3F2-related_disorder": 6,
    "POU3F2-associated_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_13|not_provided": 71,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_13|FBXL4-related_disorder": 2,
    "Mitochondrial_DNA_depletion_syndrome_13|not_specified": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_13": 57,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_13|not_specified": 4,
    "Mitochondrial_DNA_depletion_syndrome_13|not_provided|Inborn_genetic_diseases": 4,
    "Mitochondrial_DNA_depletion_syndrome_13|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Mitochondrial_DNA_depletion_syndrome_13": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_13": 2,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_13": 4,
    "Mitochondrial_DNA_depletion_syndrome_13|FBXL4-related_disorder|not_provided": 1,
    "not_provided|FBXL4-related_disorder|Mitochondrial_DNA_depletion_syndrome_13": 2,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_13|not_provided|Leigh_syndrome|Mitochondrial_encephalomyopathy|Global_developmental_delay": 1,
    "FBXL4-related_disorder": 2,
    "Leigh_syndrome|Mitochondrial_DNA_depletion_syndrome_13|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_13|not_provided|Leigh_syndrome": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_DNA_depletion_syndrome_13": 1,
    "not_provided|FBXL4-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_13|not_provided|Moyamoya_angiopathy": 1,
    "FBXL4-related_disorder|Mitochondrial_DNA_depletion_syndrome_13|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_13": 1,
    "Mitochondrial_DNA_depletion_syndrome_13|not_provided|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_13|not_provided|FBXL4-related_disorder": 1,
    "not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_13": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_DNA_depletion_syndrome_13": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_13|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome_13|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_13|not_provided": 2,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_13|not_provided|Neurodevelopmental_delay": 1,
    "Leber_congenital_amaurosis_19": 8,
    "not_specified|Laterality_defects|_autosomal_dominant": 1,
    "USP45-related_disorder": 2,
    "not_specified|Leber_congenital_amaurosis_19": 1,
    "not_provided|Leber_congenital_amaurosis_19": 1,
    "not_specified|Optic_atrophy": 2,
    "Retinal_dystrophy|not_provided|not_specified|Retinal_disorders": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_19": 1,
    "not_provided|North_Carolina_macular_dystrophy": 2,
    "North_Carolina_macular_dystrophy|maculopathy": 1,
    "Retinal_dystrophy|not_provided|North_Carolina_macular_dystrophy": 1,
    "North_Carolina_macular_dystrophy|Progressive_bifocal_chorioretinal_atrophy": 1,
    "Progressive_bifocal_chorioretinal_atrophy": 1,
    "PRDM13-related_disorder": 3,
    "PRDM13-related_disorder|not_provided": 6,
    "Cerebellar_dysfunction|_impaired_intellectual_development|_and_hypogonadotropic_hypogonadism": 3,
    "not_provided|PRDM13-related_disorder": 1,
    "not_specified|PRDM13-related_disorder|not_provided": 1,
    "Pontocerebellar_hypoplasia|_IIA_17": 3,
    "PRDM13-related_disorder|not_provided|not_specified": 1,
    "North_Carolina_macular_dystrophy|not_provided": 1,
    "PRDM13-related_disorder|not_provided|Retinal_dystrophy": 1,
    "North_Carolina_macular_dystrophy": 1,
    "Schaaf-Yang_syndrome": 72,
    "Obesity_due_to_SIM1_deficiency": 43,
    "SIM1-related_disorder": 135,
    "not_provided|SIM1-related_disorder|Obesity_due_to_SIM1_deficiency": 2,
    "SIM1-related_disorder|not_provided": 15,
    "not_provided|SIM1-related_disorder": 8,
    "Obesity_due_to_SIM1_deficiency|Microcephaly": 1,
    "Inborn_genetic_diseases|not_specified|SIM1-related_disorder": 1,
    "SIM1-related_disorder|Inborn_genetic_diseases": 6,
    "SIM1-related_disorder|Oromandibular-limb_hypogenesis_spectrum|Inborn_genetic_diseases|not_provided|not_specified|Monogenic_diabetes|Obesity_due_to_SIM1_deficiency": 1,
    "Obesity_due_to_SIM1_deficiency|Inborn_genetic_diseases": 1,
    "Obesity_due_to_SIM1_deficiency|SIM1-related_disorder": 5,
    "SIM1-related_disorder|Monogenic_diabetes": 2,
    "not_provided|not_specified|SIM1-related_disorder|Obesity_due_to_SIM1_deficiency": 1,
    "SIM1-related_disorder|Oromandibular-limb_hypogenesis_spectrum|not_provided|Obesity_due_to_SIM1_deficiency": 1,
    "Inborn_genetic_diseases|SIM1-related_disorder": 11,
    "Obesity_due_to_SIM1_deficiency|not_provided": 2,
    "Obesity_due_to_SIM1_deficiency|not_provided|SIM1-related_disorder": 1,
    "not_provided|SIM1-related_disorder|Monogenic_diabetes": 1,
    "Inborn_genetic_diseases|SIM1-related_disorder|not_provided": 2,
    "Obesity_with_Prader-Willi_like_phenotype|SIM1-related_disorder": 1,
    "SIM1-related_disorder|Inborn_genetic_diseases|Monogenic_diabetes": 1,
    "SIM1-related_disorder|Monogenic_diabetes|not_provided": 1,
    "SIM1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|SIM1-related_disorder": 1,
    "Obesity_due_to_SIM1_deficiency|not_provided|not_specified": 1,
    "SIM1-related_obesity": 1,
    "Obesity_due_to_SIM1_deficiency|SIM1-related_disorder|not_provided": 1,
    "not_provided|Obesity_due_to_SIM1_deficiency": 2,
    "Obesity_due_to_SIM1_deficiency|SIM1-related_disorder|SIM1-associated_metabolic_syndrome": 1,
    "SIM1-related_disorder|not_provided|Obesity_due_to_SIM1_deficiency": 1,
    "Obesity_due_to_SIM1_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Obesity_due_to_SIM1_deficiency": 1,
    "not_provided|Obesity_due_to_SIM1_deficiency|SIM1-related_disorder": 1,
    "SIM1-associated_metabolic_syndrome": 2,
    "Schaaf-Yang_syndrome|SIM1-related_disorder": 1,
    "not_specified|SIM1-related_disorder|Obesity_due_to_SIM1_deficiency": 1,
    "not_provided|Obesity_due_to_SIM1_deficiency|SIM1-related_disorder|Monogenic_diabetes|not_specified": 1,
    "not_provided|SIM1-related_disorder|not_specified": 1,
    "SIM1-related_disorder|Obesity_due_to_SIM1_deficiency|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_81|ASCC3-associated_disorder": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_81": 10,
    "See_cases|Intellectual_developmental_disorder|_autosomal_recessive_81": 1,
    "ASCC3-related_disorder": 2,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_81": 2,
    "not_provided|Congenital_myopathy": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_81|See_cases": 1,
    "not_provided|Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures": 2,
    "GRIK2-related_disorder": 12,
    "not_provided|GRIK2-related_disorder": 1,
    "Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures": 12,
    "Intellectual_disability|_autosomal_recessive_6|Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures": 2,
    "Intellectual_disability|_autosomal_recessive_6": 6,
    "Intellectual_disability|_autosomal_recessive_6|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_6|not_provided": 2,
    "not_specified|Intellectual_disability|GRIK2-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|GRIK2-related_disorder": 2,
    "Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures|Intellectual_disability|_autosomal_recessive_6": 1,
    "GRIK2-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_6": 1,
    "Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures|Intellectual_disability|Gait_ataxia|Severe_global_developmental_delay|not_provided|Inborn_genetic_diseases": 1,
    "GRIK2-related_neurodevelopmental_disorder|Intellectual_disability|Abnormal_cerebral_white_matter_morphology|Profound_global_developmental_delay|Seizure|Cerebral_visual_impairment|Hyperintensity_of_cerebral_white_matter_on_MRI|Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures": 1,
    "Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures|Intellectual_disability|Severe_global_developmental_delay|Hyperintensity_of_cerebral_white_matter_on_MRI": 1,
    "Intellectual_disability|_autosomal_recessive_6|Neurodevelopmental_disorder_with_impaired_language_and_ataxia_and_with_or_without_seizures|not_provided": 1,
    "HACE1-related_disorder": 4,
    "Spastic_paraplegia-severe_developmental_delay-epilepsy_syndrome|not_provided": 7,
    "Spastic_paraplegia-severe_developmental_delay-epilepsy_syndrome": 28,
    "not_provided|Spastic_paraplegia-severe_developmental_delay-epilepsy_syndrome": 4,
    "HACE1-related_disorder|not_provided": 3,
    "not_provided|HACE1-related_disorder": 3,
    "Spastic_paraplegia-severe_developmental_delay-epilepsy_syndrome|not_provided|Global_developmental_delay|Generalized_hypotonia|Seizure|Intellectual_disability": 1,
    "Psychomotor_retardation": 1,
    "Spastic_paraplegia-severe_developmental_delay-epilepsy_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|HACE1-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X": 26,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X": 2,
    "BVES-related_disorder": 3,
    "BVES-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X|not_provided": 1,
    "BVES-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X": 1,
    "Limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2X|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_26": 7,
    "POPDC3-related_disorder": 1,
    "PRDM1-related_disorder": 3,
    "ATG5-related_disorder": 1,
    "ATG5-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_25": 1,
    "not_provided|Optic_atrophy_10_with_or_without_ataxia|_intellectual_disability|_and_seizures": 3,
    "not_provided|RTN4IP1-related_disorder": 1,
    "Optic_atrophy_10_with_or_without_ataxia|_intellectual_disability|_and_seizures": 12,
    "RTN4IP1-related_disorder|not_provided": 2,
    "Optic_atrophy_10_with_or_without_ataxia|_intellectual_disability|_and_seizures|not_provided": 3,
    "Optic_atrophy|Inborn_genetic_diseases|Optic_atrophy_10_with_or_without_ataxia|_intellectual_disability|_and_seizures|not_provided": 1,
    "Macrocephaly|Global_developmental_delay|Short_stature|Chorea|not_provided": 1,
    "Optic_atrophy_10_with_or_without_ataxia|_intellectual_disability|_and_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Optic_atrophy_10_with_or_without_ataxia|_intellectual_disability|_and_seizures|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_deficiency_40": 1,
    "Combined_oxidative_phosphorylation_deficiency_40": 6,
    "not_provided|QRSL1-related_disorder": 5,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_40": 2,
    "Cardiomyopathy|_mitochondrial|Combined_oxidative_phosphorylation_deficiency_40": 2,
    "Cardiomyopathy|_mitochondrial": 1,
    "QRSL1-related_disorder|not_provided": 7,
    "Combined_oxidative_phosphorylation_deficiency_40|not_provided": 1,
    "QRSL1-related_disorder": 1,
    "not_provided|Cardiomyopathy|_mitochondrial|Combined_oxidative_phosphorylation_deficiency_40": 1,
    "Combined_oxidative_phosphorylation_deficiency_40|QRSL1-related_disorder|not_provided": 1,
    "Coenzyme_Q10_deficiency|_primary|_3": 25,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_3": 9,
    "Inborn_genetic_diseases|not_provided|Coenzyme_Q10_deficiency|_primary|_3": 2,
    "Focal_segmental_glomerulosclerosis|not_provided": 7,
    "Nephrotic_syndrome|not_specified|not_provided|Coenzyme_Q10_deficiency|_primary|_3": 1,
    "Coenzyme_Q10_deficiency|_primary|_3|not_provided|not_specified": 1,
    "PDSS2-related_disorder|Inborn_genetic_diseases|Coenzyme_Q10_deficiency|_primary|_3|not_provided": 1,
    "Coenzyme_Q10_deficiency|_primary|_3|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Coenzyme_Q10_deficiency|_primary|_3|not_provided": 7,
    "PDSS2-related_disorder|not_provided": 4,
    "not_specified|not_provided|Coenzyme_Q10_deficiency|_primary|_3": 3,
    "not_provided|Coenzyme_Q10_deficiency|_primary|_3|Inborn_genetic_diseases": 3,
    "Coenzyme_Q10_deficiency|_primary|_3|PDSS2-related_disorder": 1,
    "not_provided|PDSS2-related_disorder|Kidney_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Coenzyme_Q10_deficiency|_primary|_3|not_provided": 2,
    "not_provided|PDSS2-related_disorder": 4,
    "PDSS2-related_disorder|Kidney_disorder|not_specified|not_provided|Coenzyme_Q10_deficiency|_primary|_3": 1,
    "Coenzyme_Q10_deficiency|_primary|_3|not_specified|not_provided": 1,
    "Coenzyme_Q10_deficiency|_primary|_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Coenzyme_Q10_deficiency|_primary|_3": 1,
    "Coenzyme_Q10_deficiency|_primary|_3|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Kidney_disorder": 1,
    "not_specified|Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus": 2,
    "Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus": 4,
    "Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus|not_specified": 1,
    "Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus|SOBP-related_disorder|not_specified": 1,
    "not_specified|Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus": 1,
    "not_provided|Intellectual_disability|_anterior_maxillary_protrusion|_and_strabismus": 1,
    "SOBP-related_disorder": 3,
    "SOBP-related_disorder|not_provided|not_specified": 1,
    "not_specified|SOBP-related_disorder": 2,
    "SOBP-related_disorder|not_specified|not_provided": 1,
    "Polycystic_liver_disease_1": 130,
    "Polycystic_liver_disease_2": 176,
    "Polycystic_liver_disease_1|not_provided": 34,
    "Polycystic_liver_disease_2|not_provided": 25,
    "SEC63-related_disorder": 6,
    "Inborn_genetic_diseases|Polycystic_liver_disease_2": 2,
    "SEC63-related_disorder|Polycystic_liver_disease_2|not_provided": 2,
    "not_specified|not_provided|Polycystic_liver_disease_2": 1,
    "Polycystic_liver_disease_2|Autosomal_dominant_polycystic_liver_disease": 1,
    "Inborn_genetic_diseases|Polycystic_liver_disease_2|not_provided|SEC63-related_disorder": 1,
    "not_provided|SEC63-related_disorder|Polycystic_liver_disease_2|Autosomal_dominant_polycystic_liver_disease": 1,
    "Polycystic_liver_disease_2|SEC63-related_disorder": 1,
    "SEC63-related_disorder|not_provided|Polycystic_liver_disease_2|Autosomal_dominant_medullary_cystic_kidney_disease_with_or_without_hyperuricemia": 1,
    "Polycystic_liver_disease_2|Polycystic_liver_disease_1|not_provided": 2,
    "not_provided|not_specified|Polycystic_liver_disease_2": 1,
    "Polycystic_liver_disease_2|Glanzmann_thrombasthenia_2": 1,
    "not_provided|Polycystic_liver_disease_2|Autosomal_dominant_polycystic_liver_disease": 1,
    "SEC63-related_disorder|Polycystic_liver_disease_2|Autosomal_dominant_polycystic_liver_disease": 1,
    "Polycystic_liver_disease_2|Biliary_tract_abnormality": 1,
    "Inborn_genetic_diseases|SEC63-related_disorder": 1,
    "not_provided|Polycystic_liver_disease_2": 11,
    "SEC63-related_disorder|Polycystic_liver_disease_1|Polycystic_liver_disease_2|not_provided": 1,
    "Polycystic_liver_disease_1|Polycystic_liver_disease_2|not_provided": 3,
    "not_provided|Polycystic_liver_disease_2|Inborn_genetic_diseases": 1,
    "Biliary_tract_abnormality|not_provided|Polycystic_liver_disease_2": 1,
    "SEC63-related_disorder|not_provided": 2,
    "Polycystic_liver_disease_2|Inborn_genetic_diseases": 1,
    "Polycystic_liver_disease_2|not_provided|Autosomal_dominant_polycystic_liver_disease": 1,
    "Autosomal_dominant_polycystic_liver_disease|Inborn_genetic_diseases": 1,
    "not_provided|Polycystic_liver_disease_2|not_specified": 1,
    "SEC63-related_disorder|Polycystic_liver_disease_1": 1,
    "Polycystic_liver_disease_2|not_specified|not_provided": 3,
    "not_provided|Polycystic_liver_disease_1|Polycystic_liver_disease_2": 1,
    "not_specified|Polycystic_liver_disease_2": 1,
    "SEC63-related_disorder|Polycystic_liver_disease_1|not_provided": 1,
    "not_provided|Polycystic_liver_disease_1|not_specified|Polycystic_liver_disease_2": 1,
    "not_provided|Polycystic_liver_disease_1|not_specified": 4,
    "Biliary_tract_abnormality|Autosomal_dominant_polycystic_liver_disease|Polycystic_liver_disease_2": 1,
    "Autosomal_recessive_osteopetrosis_5": 76,
    "Osteopetrosis": 71,
    "Osteopetrosis|not_provided": 41,
    "not_provided|Autosomal_recessive_osteopetrosis_5": 14,
    "Autosomal_recessive_osteopetrosis_5|not_provided": 3,
    "not_provided|OSTM1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_5": 1,
    "Autosomal_recessive_osteopetrosis_5|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_5|not_specified": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_5|OSTM1-related_disorder": 2,
    "not_provided|OSTM1-related_disorder|Autosomal_recessive_osteopetrosis_5": 1,
    "OSTM1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_osteopetrosis_5": 2,
    "NR2E1-related_disorder": 6,
    "SNX3-related_disorder": 2,
    "ARMC2-related_disorder|not_provided": 2,
    "ARMC2-related_disorder": 9,
    "Male_infertility_with_teratozoospermia_due_to_single_gene_mutation|Spermatogenic_failure_38": 4,
    "Spermatogenic_failure_38": 1,
    "Male_infertility_with_teratozoospermia_due_to_single_gene_mutation|Spermatogenic_failure_38|Abnormal_sperm_tail_morphology": 1,
    "CD164-related_disorder": 4,
    "not_specified|CD164-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_66": 1,
    "CD164-related_disorder|not_provided": 3,
    "CD164-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|CD164-related_disorder": 1,
    "not_provided|CD164-related_disorder": 1,
    "MICAL1-related_Lateral_temporal_epilepsy|not_provided": 2,
    "Epilepsy|_familial_temporal_lobe|_1": 42,
    "Epilepsy|_familial_temporal_lobe|_1|not_provided": 4,
    "not_provided|Epilepsy|_familial_temporal_lobe|_1": 5,
    "not_provided|MICAL1-related_Lateral_temporal_epilepsy": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2": 403,
    "Inborn_genetic_diseases|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2": 16,
    "not_provided|ZBTB24-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2": 1,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|Inborn_genetic_diseases": 1,
    "ZBTB24-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2": 3,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|Inborn_genetic_diseases": 13,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2": 7,
    "Inborn_genetic_diseases|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|not_provided": 1,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|ZBTB24-related_disorder": 2,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|ZBTB24-related_disorder": 3,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|Inborn_genetic_diseases|not_specified": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|not_specified": 1,
    "not_specified|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_2|Kabuki_syndrome_1": 1,
    "Spermatogenic_failure_89": 3,
    "not_specified|Spermatogenic_failure_89": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11": 2,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11": 5,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J": 4,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|not_provided": 4,
    "Charcot-Marie-Tooth_disease_type_4J|not_provided|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J": 2,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome": 2,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_type_11|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified": 1,
    "FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Inborn_genetic_diseases|FIG4-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease_type_4|FIG4-related_disorder": 9,
    "Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4J|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_11": 1,
    "FIG4-related_disorder": 11,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_specified": 2,
    "FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J": 2,
    "Amyotrophic_lateral_sclerosis_type_11": 6,
    "Charcot-Marie-Tooth_disease_type_4J|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Yunis-Varon_syndrome": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4J": 1,
    "not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Amyotrophic_lateral_sclerosis|Yunis-Varon_syndrome": 2,
    "Charcot-Marie-Tooth_disease_type_4J|not_provided|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4": 8,
    "Leukemia|_chronic_lymphocytic|_susceptibility_to|_3|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Inborn_genetic_diseases|Bilateral_parasagittal_parieto-occipital_polymicrogyria": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4|See_cases": 1,
    "Charcot-Marie-Tooth_disease_type_4J": 6,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|FIG4-related_disorder": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis|FIG4-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease|not_provided|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Yunis-Varon_syndrome": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_11|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4|not_provided|not_specified|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease": 1,
    "Bilateral_parasagittal_parieto-occipital_polymicrogyria|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis|not_provided|FIG4-related_disorder|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|FIG4-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 4,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Bilateral_parasagittal_parieto-occipital_polymicrogyria": 2,
    "not_specified|FIG4-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|FIG4-related_disorder|Amyotrophic_lateral_sclerosis_type_11|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4J": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4J": 2,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease": 3,
    "Charcot-Marie-Tooth_disease_type_4J|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4|Yunis-Varon_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_4J": 1,
    "FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Yunis-Varon_syndrome|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4J|FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J|Bilateral_parasagittal_parieto-occipital_polymicrogyria": 1,
    "Yunis-Varon_syndrome": 6,
    "Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4": 4,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "FIG4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Yunis-Varon_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "Inborn_genetic_diseases|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis|not_provided|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Amyotrophic_lateral_sclerosis_type_11|Bilateral_parasagittal_parieto-occipital_polymicrogyria": 1,
    "FIG4-related_disorder|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4J": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Yunis-Varon_syndrome": 1,
    "Cerebral_hypomyelination": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 12,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4J|not_provided|Charcot-Marie-Tooth_disease_type_4|FIG4-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4": 1,
    "Bilateral_parasagittal_parieto-occipital_polymicrogyria|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease|not_specified": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 4,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Yunis-Varon_syndrome|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Yunis-Varon_syndrome|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|See_cases": 1,
    "not_provided|Bilateral_parasagittal_parieto-occipital_polymicrogyria|not_specified|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Yunis-Varon_syndrome": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|not_specified|FIG4-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4|FIG4-related_disorder": 1,
    "Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|FIG4-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 2,
    "Inborn_genetic_diseases|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11": 1,
    "not_provided|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Yunis-Varon_syndrome|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4J|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_11|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Yunis-Varon_syndrome": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4J|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|FIG4-related_disorder|Inborn_genetic_diseases": 1,
    "Severe_global_developmental_delay|Penile_hypospadias|Micropenis|Abnormality_of_the_skeletal_system|Failure_to_thrive": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Cerebral_hypomyelination": 1,
    "not_provided|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4J|Yunis-Varon_syndrome|Bilateral_parasagittal_parieto-occipital_polymicrogyria|Amyotrophic_lateral_sclerosis_type_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4J": 1,
    "not_provided|Charcot-Marie-Tooth_disease|FIG4-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11": 2,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|FIG4-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Yunis-Varon_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Bilateral_parasagittal_parieto-occipital_polymicrogyria|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4|not_provided|FIG4-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease_type_4|Amyotrophic_lateral_sclerosis_type_11|FIG4-related_disorder": 1,
    "FIG4-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4J|Amyotrophic_lateral_sclerosis_type_11": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4J": 1,
    "Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4J|not_provided": 1,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_11|Charcot-Marie-Tooth_disease_type_4J|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Neurodevelopmental_disorder_with_absent_language_and_variable_seizures": 16,
    "Epileptic_encephalopathy|Intellectual_disability|Neurodevelopmental_disorder_with_absent_language_and_variable_seizures": 1,
    "Intellectual_disability|Neurodevelopmental_disorder_with_absent_language_and_variable_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|Neurodevelopmental_disorder_with_absent_language_and_variable_seizures": 1,
    "WASF1-related_disorder": 11,
    "WASF1-related_disorder|not_provided|Neurodevelopmental_disorder_with_absent_language_and_variable_seizures": 1,
    "WASF1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|WASF1-related_disorder": 1,
    "WASF1-related_neurodevelopmental_disorder|not_provided": 1,
    "Pontocerebellar_hypoplasia|_type_15": 1,
    "Congenital_pontocerebellar_hypoplasia|Pontocerebellar_hypoplasia|_type_15": 1,
    "Developmental_and_epileptic_encephalopathy|_87": 15,
    "CDK19-related_disorder": 5,
    "Inborn_genetic_diseases|CDK19-related_disorder|Developmental_and_epileptic_encephalopathy|_87": 1,
    "Developmental_and_epileptic_encephalopathy|_87|not_provided": 1,
    "not_provided|REV3L-related_disorder": 10,
    "REV3L-related_disorder": 26,
    "REV3L-related_disorder|not_provided": 12,
    "Candidiasis|_familial|_8": 215,
    "Psoriasis_13|_susceptibility_to": 2,
    "not_specified|Candidiasis|_familial|_8": 12,
    "not_provided|Candidiasis|_familial|_8": 3,
    "Discoid_lupus_erythematosus": 1,
    "Candidiasis|_familial|_8|TRAF3IP2-related_disorder": 4,
    "TRAF3IP2-related_disorder|Candidiasis|_familial|_8|not_provided": 1,
    "Candidiasis|_familial|_8|not_specified": 11,
    "Candidiasis|_familial|_8|not_provided": 1,
    "not_specified|Candidiasis|_familial|_8|not_provided": 1,
    "Psoriasis_13|_susceptibility_to|Candidiasis|_familial|_8|not_specified": 2,
    "Psoriasis_13|_susceptibility_to|Candidiasis|_familial|_8": 1,
    "TRAF3IP2-related_disorder|Candidiasis|_familial|_8": 1,
    "not_provided|Psoriasis_13|_susceptibility_to|Candidiasis|_familial|_8": 1,
    "Candidiasis|_familial|_8|not_provided|not_specified": 1,
    "Psoriasis_13|_susceptibility_to|Candidiasis|_familial|_8|not_specified|not_provided": 1,
    "Progressive_pseudorheumatoid_dysplasia|not_provided": 19,
    "not_provided|Progressive_pseudorheumatoid_dysplasia": 9,
    "Progressive_pseudorheumatoid_dysplasia": 23,
    "not_provided|CCN6-related_disorder|Inborn_genetic_diseases|Progressive_pseudorheumatoid_dysplasia|not_specified": 1,
    "not_specified|CCN6-related_disorder|not_provided|Progressive_pseudorheumatoid_dysplasia|Inborn_genetic_diseases": 1,
    "not_provided|Progressive_pseudorheumatoid_dysplasia|CCN6-related_disorder": 2,
    "See_cases|not_provided|Progressive_pseudorheumatoid_dysplasia": 1,
    "not_specified|Progressive_pseudorheumatoid_dysplasia": 1,
    "not_specified|not_provided|Progressive_pseudorheumatoid_dysplasia|CCN6-related_disorder": 1,
    "not_provided|CCN6-related_disorder": 1,
    "CCN6-related_disorder|not_provided": 1,
    "CCN6-related_disorder": 1,
    "Inborn_genetic_diseases|Progressive_pseudorheumatoid_dysplasia|not_provided": 1,
    "not_provided|CCN6-related_disorder|Progressive_pseudorheumatoid_dysplasia": 1,
    "Progressive_pseudorheumatoid_dysplasia|not_provided|CCN6-related_disorder": 1,
    "not_provided|Progressive_pseudorheumatoid_dysplasia|Inborn_genetic_diseases": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1JJ": 557,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 179,
    "Cardiovascular_phenotype|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|not_provided|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|Cardiovascular_phenotype": 9,
    "Dilated_cardiomyopathy_1JJ|not_specified|not_provided|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|LAMA4-related_disorder|not_specified|Dilated_cardiomyopathy_1JJ": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 125,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified": 9,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified|not_provided": 6,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 8,
    "not_provided|Dilated_cardiomyopathy_1JJ": 17,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|not_provided": 21,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified": 23,
    "not_specified|Dilated_cardiomyopathy_1JJ": 21,
    "not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided": 29,
    "Dilated_cardiomyopathy_1JJ|not_provided": 17,
    "LAMA4-related_disorder": 4,
    "Cardiovascular_phenotype|LAMA4-related_disorder": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 1,
    "not_provided|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 20,
    "not_specified|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 4,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|not_specified": 11,
    "LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|Cardiomyopathy": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 23,
    "LAMA4-related_disorder|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1JJ|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1JJ": 5,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1JJ|not_specified": 3,
    "Dilated_cardiomyopathy_1JJ|not_provided|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1JJ": 15,
    "Cardiomyopathy|Dilated_cardiomyopathy_1JJ|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|LAMA4-related_disorder|not_specified|Dilated_cardiomyopathy_1JJ|not_provided": 1,
    "not_provided|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1JJ": 1,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 2,
    "Dilated_cardiomyopathy_1JJ|not_specified|not_provided": 5,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1JJ|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|not_provided|Cardiovascular_phenotype": 17,
    "Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 3,
    "not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified|not_provided|Cardiomyopathy": 4,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Cardiomyopathy|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1JJ|not_specified|Cardiovascular_phenotype": 1,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided": 1,
    "Spinocerebellar_ataxia_type_19/22|Brugada_syndrome_9|Familial_atrial_fibrillation|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|not_provided": 1,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1JJ|not_provided|Cardiomyopathy": 1,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|not_specified|Premature_ventricular_contraction|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|LAMA4-related_disorder": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1JJ": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|Cardiomyopathy|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1JJ|not_specified": 2,
    "not_specified|Dilated_cardiomyopathy_1JJ|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1JJ": 5,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1JJ|not_provided|LAMA4-related_disorder|Cardiovascular_phenotype": 1,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "not_provided|LAMA4-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1JJ|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1JJ": 2,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "not_provided|Dilated_cardiomyopathy_1JJ|not_specified|LAMA4-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|Wolff-Parkinson-White_pattern": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ": 2,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 2,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|LAMA4-related_disorder|not_specified": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 5,
    "not_provided|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1JJ|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|not_specified|Cardiomyopathy": 2,
    "not_provided|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ": 1,
    "LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1JJ": 1,
    "Cardiovascular_phenotype|Ventricular_tachycardia|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1JJ|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1JJ|not_provided": 3,
    "LAMA4-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1JJ|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|Cardiomyopathy": 1,
    "Brugada_syndrome|Dilated_cardiomyopathy_1JJ|not_provided": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder": 2,
    "Dilated_cardiomyopathy_1JJ|not_provided|LAMA4-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_3B": 66,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided": 1,
    "LAMA4-related_disorder|not_specified|Dilated_cardiomyopathy_1JJ|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|Cardiomyopathy|LAMA4-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|LAMA4-related_disorder": 1,
    "Dilated_cardiomyopathy_1JJ|not_provided|Primary_dilated_cardiomyopathy|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 1,
    "LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|not_specified|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype|not_provided": 1,
    "LAMA4-related_disorder|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1JJ|not_specified|LAMA4-related_disorder": 1,
    "not_specified|Dilated_cardiomyopathy_1JJ|Cardiomyopathy": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1JJ|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1JJ|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1JJ|not_specified|not_provided|LAMA4-related_disorder": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1JJ": 1,
    "Dilated_cardiomyopathy_1JJ|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1JJ|LAMA4-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|LAMA4-related_disorder|Dilated_cardiomyopathy_1JJ|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1JJ|Hypertrophic_cardiomyopathy_1": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1JJ": 1,
    "HDAC2-related_disorder": 6,
    "Metaphyseal_chondrodysplasia": 6,
    "not_provided|Metaphyseal_chondrodysplasia|_Schmid_type": 20,
    "not_provided|Metaphyseal_chondrodysplasia|Metaphyseal_chondrodysplasia|_Schmid_type|not_specified": 1,
    "not_specified|not_provided|Metaphyseal_chondrodysplasia|_Schmid_type": 1,
    "COL10A1-related_disorder|not_provided": 2,
    "Metaphyseal_chondrodysplasia|_Schmid_type|not_provided": 15,
    "Inborn_genetic_diseases|Metaphyseal_chondrodysplasia|_Schmid_type": 4,
    "COL10A1-related_disorder": 5,
    "not_provided|not_specified|Metaphyseal_chondrodysplasia|_Schmid_type": 3,
    "not_specified|Metaphyseal_chondrodysplasia|_Schmid_type|not_provided": 2,
    "COL10A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Metaphyseal_chondrodysplasia|_Schmid_type": 4,
    "not_provided|COL10A1-related_disorder|Metaphyseal_chondrodysplasia|_Schmid_type": 1,
    "COL10A1-related_disorder|not_provided|Inborn_genetic_diseases|Nager_syndrome": 1,
    "Inborn_genetic_diseases|COL10A1-related_disorder|not_provided": 2,
    "not_provided|COL10A1-related_disorder": 2,
    "not_provided|Metaphyseal_chondrodysplasia|_Schmid_type|Inborn_genetic_diseases": 1,
    "COL10A1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Metaphyseal_chondrodysplasia|_Schmid_type|Inborn_genetic_diseases|not_provided": 2,
    "Metaphyseal_chondrodysplasia|_Schmid_type|not_provided|Inborn_genetic_diseases": 2,
    "COL10A1-related_disorder|Metaphyseal_chondrodysplasia|_Schmid_type|not_provided": 2,
    "Metaphyseal_chondrodysplasia|_Schmid_type|not_provided|See_cases": 1,
    "not_provided|Metaphyseal_chondrodysplasia|not_specified": 1,
    "not_specified|Metaphyseal_chondrodysplasia|_Schmid_type|not_provided|COL10A1-related_disorder": 1,
    "not_provided|Metaphyseal_chondrodysplasia|_Schmid_type|not_specified": 1,
    "not_specified|not_provided|Sudden_infant_death-dysgenesis_of_the_testes_syndrome|TSPYL1-related_disorder": 1,
    "TSPYL1-related_disorder": 2,
    "Sudden_infant_death-dysgenesis_of_the_testes_syndrome": 8,
    "not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 16,
    "TSPYL1-related_disorder|not_provided": 1,
    "not_provided|DSE-related_disorder": 3,
    "DSE-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 8,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2": 167,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_specified|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_specified": 8,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided": 15,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 1,
    "not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 9,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome": 2,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided": 2,
    "not_specified|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 1,
    "not_provided|DSE-related_disorder|not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 1,
    "DSE-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided|not_specified": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome|not_provided": 2,
    "not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_specified": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "DSE-related_disorder|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_specified": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|DSE-related_disorder|not_provided|not_specified": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_specified|DSE-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2|DSE-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|Inborn_genetic_diseases|not_specified": 2,
    "Ehlers-Danlos_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided|DSE-related_disorder|Inborn_genetic_diseases": 1,
    "DSE-related_disorder|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_provided|not_specified": 1,
    "not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type_2|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|DSE-related_disorder|not_specified|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_2|DSE-related_disorder|Ehlers-Danlos_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 1,
    "not_provided|DSE-related_disorder|Ehlers-Danlos_syndrome|_musculocontractural_type_2|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type|Ehlers-Danlos_syndrome|_musculocontractural_type_2": 1,
    "Primary_ciliary_dyskinesia_11": 26,
    "not_provided|Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia": 1,
    "RSPH4A-related_disorder|Primary_ciliary_dyskinesia_11|not_provided|Primary_ciliary_dyskinesia|not_specified": 1,
    "RSPH4A-related_disorder": 2,
    "Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia": 14,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 13,
    "Primary_ciliary_dyskinesia|RSPH4A-related_disorder": 3,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 5,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 1,
    "RSPH4A-related_disorder|Primary_ciliary_dyskinesia_11|Kartagener_syndrome|not_provided|Primary_ciliary_dyskinesia": 1,
    "Neurodevelopmental_delay|Primary_ciliary_dyskinesia": 1,
    "RSPH4A-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_11": 2,
    "Primary_ciliary_dyskinesia_11|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11|not_provided": 2,
    "Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 3,
    "Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia|not_specified": 1,
    "not_specified|Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 1,
    "not_specified|Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11|not_specified": 1,
    "RSPH4A-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_11": 1,
    "not_provided|RSPH4A-related_disorder|Primary_ciliary_dyskinesia_11|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_11|not_specified|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia_11|not_specified": 1,
    "not_specified|Monogenic_diabetes|not_provided|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome": 1,
    "RFX6-related_disorder": 12,
    "not_provided|Monogenic_diabetes": 77,
    "RFX6-related_disorder|not_provided|not_specified": 2,
    "Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome": 13,
    "not_provided|RFX6-related_disorder": 4,
    "RFX6-related_disorder|not_provided": 5,
    "Diabetes_mellitus|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome": 1,
    "Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|Inborn_genetic_diseases|RFX6-related_disorder": 1,
    "not_provided|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|Inborn_genetic_diseases|RFX6-related_disorder": 1,
    "RFX6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RFX6-related_disorder|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome": 1,
    "Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_provided": 4,
    "not_provided|RFX6-related_disorder|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_specified": 1,
    "RFX6-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|RFX6-related_disorder": 1,
    "not_specified|Monogenic_diabetes|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_provided": 1,
    "Monogenic_diabetes|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_specified|not_provided|RFX6-related_disorder": 1,
    "Monogenic_diabetes|not_provided|not_specified|RFX6-related_disorder": 1,
    "not_provided|not_specified|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome": 1,
    "not_specified|Monogenic_diabetes|not_provided|RFX6-related_disorder": 1,
    "not_provided|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome": 1,
    "Monogenic_diabetes|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_provided": 2,
    "Hypoplastic_pancreas-intestinal_atresia-hypoplastic_gallbalder_syndrome|not_provided|Monogenic_diabetes|RFX6-related_disorder": 1,
    "not_specified|ROS1-related_disorder": 1,
    "ROS1-related_disorder": 4,
    "ROS1-related_disorder|not_specified|not_provided|Abnormal_brain_morphology": 1,
    "Congenital_disorder_of_glycosylation|_type_IAA": 294,
    "Intellectual_disability|_autosomal_dominant_55|_with_seizures|Congenital_disorder_of_glycosylation|_type_IAA": 4,
    "Congenital_disorder_of_glycosylation|_type_IAA|NUS1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|_type_IAA|Intellectual_disability|_autosomal_dominant_55|_with_seizures": 1,
    "NUS1-related_disorder": 7,
    "Congenital_disorder_of_glycosylation|_type_IAA|Inborn_genetic_diseases": 12,
    "Intellectual_disability|_autosomal_dominant_55|_with_seizures": 26,
    "Congenital_disorder_of_glycosylation|_type_IAA|not_provided": 4,
    "NUS1-related_disorder|Congenital_disorder_of_glycosylation|_type_IAA|not_provided": 2,
    "Congenital_disorder_of_glycosylation|_type_IAA|not_provided|not_specified": 1,
    "not_provided|Congenital_disorder_of_glycosylation|_type_IAA": 14,
    "Congenital_disorder_of_glycosylation|_type_IAA|not_specified": 2,
    "Intellectual_disability|_autosomal_dominant_55|_with_seizures|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|_type_IAA": 8,
    "Congenital_disorder_of_glycosylation|_type_IAA|Inborn_genetic_diseases|not_provided": 2,
    "NUS1-related_disorder|Congenital_disorder_of_glycosylation|_type_IAA": 2,
    "Congenital_disorder_of_glycosylation|_type_IAA|not_provided|NUS1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Congenital_disorder_of_glycosylation|_type_IAA": 1,
    "Congenital_disorder_of_glycosylation|_type_IAA|not_provided|Intellectual_disability|_autosomal_dominant_55|_with_seizures": 1,
    "Intellectual_disability|_autosomal_dominant_55|_with_seizures|Congenital_disorder_of_glycosylation|_type_IAA|NUS1-related_disorder|not_provided": 1,
    "Congenital_bilateral_perisylvian_syndrome": 3,
    "Congenital_disorder_of_glycosylation|_type_IAA|not_specified|not_provided": 1,
    "Congenital_disorder_of_glycosylation|_type_IAA|Intellectual_disability|_autosomal_dominant_55|_with_seizures|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_55|_with_seizures": 2,
    "not_provided|Congenital_disorder_of_glycosylation|_type_IAA|Inborn_genetic_diseases": 1,
    "NUS1-related_epilepsy-myoclonus-ataxia_syndrome|Congenital_disorder_of_glycosylation|_type_IAA": 1,
    "Intellectual_disability|_autosomal_dominant_55|_with_seizures|Congenital_disorder_of_glycosylation|_type_IAA|NUS1-related_disorder|Congenital_disorder_of_glycosylation": 1,
    "Lissencephaly_10": 18,
    "Lissencephaly_10|Inborn_genetic_diseases": 1,
    "CEP85L-related_disorder": 7,
    "not_provided|Lissencephaly_10": 2,
    "Dilated_cardiomyopathy_1P": 48,
    "Hypertrophic_cardiomyopathy_18|Dilated_cardiomyopathy_1P": 1,
    "Dilated_cardiomyopathy_1P|Hypertrophic_cardiomyopathy_18": 8,
    "PLN-related_disorder|Dilated_cardiomyopathy_1P|not_provided": 1,
    "Hypertrophic_cardiomyopathy_18|Dilated_cardiomyopathy_1P|PLN-related_disorder": 1,
    "Lissencephaly_10|not_specified|not_provided|Dilated_cardiomyopathy_1P": 1,
    "Dilated_cardiomyopathy_1P|not_provided": 3,
    "Dilated_cardiomyopathy_1P|Hypertrophic_cardiomyopathy_18|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1P": 1,
    "not_specified|Dilated_cardiomyopathy_1P": 3,
    "not_provided|Dilated_cardiomyopathy_1P|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1P": 1,
    "Dilated_cardiomyopathy_1P|not_specified": 1,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1P": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1P": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1P": 1,
    "PLN-related_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_18|Dilated_cardiomyopathy_1P|Primary_dilated_cardiomyopathy|SUDDEN_INFANT_DEATH_SYNDROME|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Dilated_cardiomyopathy_1P|Cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1P|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1P": 4,
    "Hypertrophic_cardiomyopathy_18|Dilated_cardiomyopathy_1P|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1P|Cardiovascular_phenotype": 5,
    "Dilated_cardiomyopathy_1P|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_18|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1P|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_18": 2,
    "not_provided|Dilated_cardiomyopathy_1P": 3,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1P|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1P|not_provided": 1,
    "PLN-related_disorder|Cardiovascular_phenotype|Intrinsic_cardiomyopathy|Sudden_cardiac_death|Cardiac_arrest|Hypertrophic_cardiomyopathy_18|Dilated_cardiomyopathy_1P|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1P|Hypertrophic_cardiomyopathy_18|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1P|PLN-related_disorder|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1P|Hypertrophic_cardiomyopathy_18|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant": 425,
    "not_provided|Dilated_cardiomyopathy_1P|Hypertrophic_cardiomyopathy_18": 1,
    "Dilated_cardiomyopathy_1P|not_provided|Hypertrophic_cardiomyopathy_18": 1,
    "not_provided|CEP85L-related_disorder": 1,
    "Inborn_genetic_diseases|Lissencephaly_10": 1,
    "Posterior_Predominant_Lissencephaly|Lissencephaly_10": 4,
    "Lissencephaly|Thick_corpus_callosum": 1,
    "Posterior_Predominant_Lissencephaly|Neurodevelopmental_disorder": 1,
    "Posterior_Predominant_Lissencephaly": 3,
    "Lissencephaly_10|Lissencephaly": 1,
    "Inborn_genetic_diseases|CEP85L-related_disorder": 1,
    "Lissencephaly_10|Posterior_Predominant_Lissencephaly": 1,
    "MCM9-related_disorder|not_provided": 4,
    "MCM9-related_disorder": 5,
    "46|XX_ovarian_dysgenesis-short_stature_syndrome|Premature_ovarian_failure_1": 1,
    "46|XX_ovarian_dysgenesis-short_stature_syndrome": 9,
    "Premature_ovarian_failure_1": 1,
    "46|XX_ovarian_dysgenesis-short_stature_syndrome|not_provided": 1,
    "Premature_ovarian_insufficiency|not_specified|MCM9-related_disorder|Premature_ovarian_failure|not_provided": 1,
    "46|XX_ovarian_dysgenesis-short_stature_syndrome|Inborn_genetic_diseases": 1,
    "46|XX_ovarian_dysgenesis-short_stature_syndrome|Non-obstructive_azoospermia|Premature_ovarian_failure_1": 1,
    "Joubert_syndrome_36": 11,
    "TBC1D32-related_disorder": 4,
    "not_provided|TBC1D32-related_disorder": 2,
    "ALSAHAN-HARRIS_SYNDROME": 1,
    "Isolated_optic_nerve_hypoplasia": 2,
    "not_provided|ALSAHAN-HARRIS_SYNDROME|Inborn_genetic_diseases": 1,
    "Hypopituitarism|Orofaciodigital_syndrome_IX|Ciliopathy": 1,
    "ALSAHAN-HARRIS_SYNDROME|Orofaciodigital_syndrome_IX|not_provided": 1,
    "RETINITIS_PIGMENTOSA_100": 4,
    "not_provided|Orofaciodigital_syndrome_IX": 1,
    "TBC1D32-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Oculodentodigital_dysplasia|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3": 6,
    "Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia": 2,
    "Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|Oculodentodigital_dysplasia": 24,
    "Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia|Syndactyly_type_3": 5,
    "not_provided|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|Oculodentodigital_dysplasia": 3,
    "not_provided|Oculodentodigital_dysplasia|Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1": 1,
    "Oculodentodigital_dysplasia|_autosomal_recessive": 142,
    "Oculodentodigital_dysplasia|_autosomal_recessive|not_specified": 4,
    "Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia": 1,
    "Oculodentodigital_dysplasia": 18,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia": 3,
    "Oculodentodigital_dysplasia|_autosomal_recessive|not_provided": 13,
    "Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive": 4,
    "not_provided|Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Erythrokeratodermia_variabilis_et_progressiva_3|Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive|Atrioventricular_septal_defect_and_common_atrioventricular_junction|Craniometaphyseal_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3": 1,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Erythrokeratodermia_variabilis_et_progressiva_3": 1,
    "Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Craniometaphyseal_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive|Syndactyly_type_3|Erythrokeratodermia_variabilis_et_progressiva_3": 1,
    "GJA1-related_disorder": 5,
    "not_provided|Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive": 4,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|Oculodentodigital_dysplasia": 1,
    "GJA1-related_disorder|not_provided": 2,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Syndactyly_type_3|Oculodentodigital_dysplasia|Erythrokeratodermia_variabilis_et_progressiva_3|Craniometaphyseal_dysplasia|_autosomal_recessive": 1,
    "Atrioventricular_septal_defect_and_common_atrioventricular_junction": 2,
    "Syndactyly_type_3": 1,
    "Cutaneous_finger_syndactyly|Intellectual_disability|Anteverted_nares|Bilateral_microphthalmos": 1,
    "not_provided|Oculodentodigital_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|Oculodentodigital_dysplasia": 3,
    "not_provided|not_specified|Oculodentodigital_dysplasia|_autosomal_recessive": 1,
    "Finger_syndactyly|Underdeveloped_nasal_alae|Narrow_nasal_bridge|Cleft_upper_lip|Edema_of_the_dorsum_of_feet|Sparse_hair|4-5_finger_cutaneous_syndactyly|Atrioventricular_septal_defect_and_common_atrioventricular_junction": 1,
    "not_provided|Oculodentodigital_dysplasia|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "Oculodentodigital_dysplasia|_autosomal_recessive|GJA1-related_disorder": 1,
    "GJA1-related_disorder|Inborn_genetic_diseases": 1,
    "Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia|Syndactyly_type_3": 2,
    "Erythrokeratodermia_variabilis_et_progressiva_3|Oculodentodigital_dysplasia|_autosomal_recessive": 1,
    "Oculodentodigital_dysplasia|GJA1-related_disorder": 1,
    "not_provided|Oculodentodigital_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia|Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1": 1,
    "Craniometaphyseal_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia|_autosomal_recessive|not_provided": 1,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia|Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1|not_specified|not_provided": 1,
    "Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|not_provided": 1,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Cleft_palate|not_provided": 1,
    "GJA1-related_disorder|Oculodentodigital_dysplasia|_autosomal_recessive": 1,
    "not_specified|not_provided|Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive": 1,
    "Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive|Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1": 1,
    "not_provided|Oculodentodigital_dysplasia": 1,
    "not_provided|Inborn_genetic_diseases|Oculodentodigital_dysplasia|_autosomal_recessive": 2,
    "not_provided|Oculodentodigital_dysplasia|Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia|_autosomal_recessive|GJA1-related_disorder": 1,
    "Oculodentodigital_dysplasia|_autosomal_recessive|not_provided|Syndactyly_type_3|Craniometaphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Oculodentodigital_dysplasia|Erythrokeratodermia_variabilis_et_progressiva_3": 1,
    "Oculodentodigital_dysplasia|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Oculodentodigital_dysplasia|_autosomal_recessive": 2,
    "Oculodentodigital_dysplasia|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|GJA1-related_disorder|Oculodentodigital_dysplasia|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Syndactyly_type_5": 1,
    "not_provided|Oculodentodigital_dysplasia|_autosomal_recessive|Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Oculodentodigital_dysplasia|Hypoplastic_left_heart_syndrome_1|Syndactyly_type_3|Craniometaphyseal_dysplasia|_autosomal_recessive|Atrioventricular_septal_defect_and_common_atrioventricular_junction|Erythrokeratodermia_variabilis_et_progressiva_3": 1,
    "Atrioventricular_septal_defect_and_common_atrioventricular_junction|Oculodentodigital_dysplasia|_autosomal_recessive|GJA1-related_disorder": 1,
    "Inborn_genetic_diseases|Oculodentodigital_dysplasia|Syndactyly_type_3|Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_provided|Oculodentodigital_dysplasia|_autosomal_recessive|Oculodentodigital_dysplasia|Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Erythrokeratodermia_variabilis_et_progressiva_3|Syndactyly_type_3|Atrioventricular_septal_defect_and_common_atrioventricular_junction|Craniometaphyseal_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1": 1,
    "not_provided|Atrioventricular_septal_defect_and_common_atrioventricular_junction|Oculodentodigital_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_3|Syndactyly_type_3|Craniometaphyseal_dysplasia|_autosomal_recessive|Autosomal_dominant_palmoplantar_keratoderma_and_congenital_alopecia|Oculodentodigital_dysplasia|Oculodentodigital_dysplasia|_autosomal_recessive|Hypoplastic_left_heart_syndrome_1|Atrioventricular_septal_defect_and_common_atrioventricular_junction|not_provided": 1,
    "not_specified|Syndactyly|Oculodentodigital_dysplasia|Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia|_autosomal_recessive|not_provided": 1,
    "Syndactyly|Hypoplastic_left_heart_syndrome_1|Oculodentodigital_dysplasia": 3,
    "Syndactyly|Oculodentodigital_dysplasia|Hypoplastic_left_heart_syndrome_1": 3,
    "Oculodentodigital_dysplasia|Hypoplastic_left_heart_syndrome_1|Syndactyly": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 5,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5": 15,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 6,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|TRDN-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 8,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype": 8,
    "TRDN-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "TRDN-related_disorder": 6,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "not_provided|TRDN-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|TRDN-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 12,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 2,
    "not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|TRDN-related_disorder|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|TRDN-related_disorder|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided": 1,
    "not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype|not_specified": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|TRDN-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 3,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|TRDN-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 2,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "not_specified|TRDN-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|TRDN-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 4,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|not_provided|TRDN-related_disorder": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|TRDN-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|TRDN-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|TRDN-related_disorder|not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_specified|Cardiovascular_phenotype": 1,
    "TRDN-related_disorder|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|TRDN-related_disorder": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Catecholaminergic_polymorphic_ventricular_tachycardia_5|not_provided|Cardiovascular_phenotype": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_5": 1,
    "TRDN-related_disorder|not_provided": 1,
    "Deficiency_of_butyryl-CoA_dehydrogenase": 316,
    "sellar_metastasis_from_primary_bronchial_carcinoid_tumor": 7,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 30,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided": 3,
    "Congenital_Muscular_Dystrophy|_LAMA2-related": 5,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy": 2,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 55,
    "LAMA2-related_muscular_dystrophy": 2991,
    "LAMA2-related_muscular_dystrophy|not_provided": 137,
    "Merosin_deficient_congenital_muscular_dystrophy": 173,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided": 22,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 38,
    "not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 8,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 5,
    "LAMA2-related_muscular_dystrophy|not_provided|Inborn_genetic_diseases": 12,
    "not_provided|LAMA2-related_muscular_dystrophy": 132,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided|Inborn_genetic_diseases|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_muscular_dystrophy|not_specified": 33,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 35,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy": 38,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided": 8,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 2,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 155,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 17,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 5,
    "Inborn_genetic_diseases|not_provided|LAMA2-related_muscular_dystrophy": 10,
    "LAMA2-related_disorder|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 4,
    "LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases": 30,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 18,
    "not_provided|LAMA2-related_muscular_dystrophy|not_specified": 9,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_provided": 7,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 5,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 18,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_specified": 2,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_provided": 2,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided|not_specified": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 14,
    "LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 7,
    "Primary_dilated_cardiomyopathy|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|LAMA2-related_muscular_dystrophy|not_provided": 2,
    "not_provided|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy": 5,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 12,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 8,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided|LAMA2-related_muscular_dystrophy|not_specified|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Congenital_Muscular_Dystrophy|_LAMA2-related": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 5,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_specified|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 2,
    "Merosin_deficient_congenital_muscular_dystrophy|not_specified": 4,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 7,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 1,
    "not_provided|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 6,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 5,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Inborn_genetic_diseases": 1,
    "Congenital_Muscular_Dystrophy|_LAMA2-related|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_disorder": 11,
    "not_specified|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 3,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy": 14,
    "not_provided|LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases": 6,
    "LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 4,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy": 7,
    "Merosin_deficient_congenital_muscular_dystrophy|Hypotonia": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 2,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Limb-girdle_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|LAMA2-related_muscular_dystrophy": 5,
    "LAMA2-related_disorder|Inborn_genetic_diseases|not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 11,
    "LAMA2-related_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy": 2,
    "LAMA2-related_disorder|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Intellectual_disability": 1,
    "LAMA2-related_disorder|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_provided|not_specified": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases": 3,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided": 1,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_specified|not_provided": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Inborn_genetic_diseases|Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|not_specified": 2,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 3,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 6,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_specified|not_provided|LAMA2-related_muscular_dystrophy|LAMA2-related_disorder": 1,
    "Inborn_genetic_diseases|Merosin_deficient_congenital_muscular_dystrophy|not_specified": 1,
    "LAMA2-related_disorder|not_specified|not_provided|LAMA2-related_muscular_dystrophy": 2,
    "not_specified|LAMA2-related_muscular_dystrophy": 30,
    "not_specified|not_provided|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|not_provided": 4,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Inborn_genetic_diseases|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided": 2,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_provided": 3,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|LAMA2-related_muscular_dystrophy": 4,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 7,
    "LAMA2-related_muscular_dystrophy|not_specified|not_provided": 9,
    "not_specified|Myalgia|Exercise-induced_myalgia|Elevated_circulating_creatine_kinase_concentration|LAMA2-related_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Intellectual_disability": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 2,
    "Intellectual_disability|not_provided|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 5,
    "LAMA2-related_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|LAMA2-related_muscular_dystrophy|not_provided": 3,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 2,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy": 2,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided": 10,
    "LAMA2-related_muscular_dystrophy|LAMA2-related_disorder|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_disorder|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 2,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided|not_specified|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|LAMA2-related_disorder|not_provided": 2,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 4,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|not_provided": 1,
    "not_provided|LAMA2-related_disorder": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_provided": 8,
    "LAMA2-related_muscular_dystrophy|not_provided|Inborn_genetic_diseases|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|Intellectual_disability|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided|Intellectual_disability": 1,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 2,
    "LAMA2-related_muscular_dystrophy|not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy": 2,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Intellectual_disability|not_specified|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "not_provided|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 2,
    "LAMA2-related_disorder|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 2,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Qualitative_or_quantitative_defects_of_merosin|not_provided": 1,
    "Congenital_Muscular_Dystrophy|_LAMA2-related|LAMA2-related_muscular_dystrophy": 3,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_congenital|_merosin_deficient_or_partially_deficient": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|LAMA2-related_disorder|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|LAMA2-related_disorder": 5,
    "LAMA2-related_muscular_dystrophy|not_specified|LAMA2-related_disorder|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Abnormality_of_the_musculature": 2,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided": 4,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided|not_specified": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_specified|not_provided": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_disorder|not_specified|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_provided|not_specified": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|Intellectual_disability": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 2,
    "Merosin_deficient_congenital_muscular_dystrophy|Congenital_Muscular_Dystrophy|_LAMA2-related|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 2,
    "not_provided|LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Hypertrophic_cardiomyopathy": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided": 1,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 2,
    "Intellectual_disability|LAMA2-related_muscular_dystrophy": 3,
    "LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy": 3,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|not_specified": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|LAMA2-related_disorder": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_specified|not_provided": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|LAMA2-related_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "not_provided|Congenital_Muscular_Dystrophy|_LAMA2-related|not_specified|LAMA2-related_muscular_dystrophy": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "Inborn_genetic_diseases|Distal_myopathy": 2,
    "Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 2,
    "LAMA2-related_disorder|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Polymicrogyria|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases|not_provided|Abnormality_of_the_musculature": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy|LAMA2-related_disorder": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 2,
    "LAMA2-related_muscular_dystrophy|Rare_genetic_intellectual_disability|Inborn_genetic_diseases": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_specified|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Polymicrogyria": 1,
    "LAMA2-related_disorder|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_disorder|not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|See_cases": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 1,
    "See_cases|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_muscular_dystrophy|LAMA2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|Limb-girdle_muscular_dystrophy|LAMA2-related_disorder|not_provided": 1,
    "not_provided|Abnormality_of_the_musculature": 3,
    "Inborn_genetic_diseases|not_provided|LAMA2-related_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Intellectual_disability": 1,
    "not_specified|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|not_specified|LAMA2-related_muscular_dystrophy|Limb-girdle_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|Intellectual_disability": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|not_specified": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Intellectual_disability": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_specified|not_provided": 2,
    "LAMA2-related_disorder|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "Qualitative_or_quantitative_defects_of_merosin|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_disorder|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 2,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases|not_specified": 1,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|not_specified": 2,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|not_provided": 2,
    "not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_specified|Inborn_genetic_diseases": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 1,
    "Myalgia|Exercise-induced_myalgia|Elevated_circulating_creatine_kinase_concentration|LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Primary_dilated_cardiomyopathy|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Primary_dilated_cardiomyopathy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|LAMA2-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|not_provided": 1,
    "not_provided|LAMA2-related_disorder|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 2,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_disorder|LAMA2-related_muscular_dystrophy|not_provided|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "not_specified|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_specified|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_disorder|not_specified|LAMA2-related_muscular_dystrophy": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|LAMA2-related_disorder|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy|LAMA2-related_disorder|Congenital_Muscular_Dystrophy|_LAMA2-related|Inborn_genetic_diseases": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|not_specified|LAMA2-related_muscular_dystrophy": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy|not_provided|LAMA2-related_disorder": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|LAMA2-related_muscular_dystrophy": 2,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|Inborn_genetic_diseases": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|LAMA2-related_disorder|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "not_specified|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_specified|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy": 1,
    "not_specified|not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided|LAMA2-related_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Distal_myopathy|LAMA2-related_muscular_dystrophy": 1,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|not_provided|LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_disorder|not_specified|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "not_specified|not_provided|LAMA2-related_disorder|LAMA2-related_muscular_dystrophy": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|LAMA2-related_muscular_dystrophy|not_specified|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_muscular_dystrophy|Primary_dilated_cardiomyopathy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Primary_dilated_cardiomyopathy|Inborn_genetic_diseases|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy|LAMA2-related_muscular_dystrophy|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Merosin_deficient_congenital_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy|not_specified": 1,
    "not_specified|LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|Intellectual_disability|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|not_provided": 1,
    "LAMA2-related_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy|Inborn_genetic_diseases|LAMA2-related_muscular_dystrophy|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency": 1,
    "LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|not_provided|not_specified": 1,
    "LAMA2-related_muscular_dystrophy|Inborn_genetic_diseases|not_provided|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "LAMA2-related_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|LAMA2-related_muscular_dystrophy|Congenital_muscular_dystrophy_due_to_partial_LAMA2_deficiency|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_23|Merosin_deficient_congenital_muscular_dystrophy": 1,
    "Congenital_Muscular_Dystrophy|_LAMA2-related|not_provided": 1,
    "ARHGAP18-related_disorder": 1,
    "Arginase_deficiency": 461,
    "Arginase_deficiency|not_provided": 8,
    "not_provided|Arginase_deficiency": 20,
    "Arginase_deficiency|not_specified": 6,
    "Inborn_genetic_diseases|not_provided|Arginase_deficiency": 2,
    "Arginase_deficiency|ARG1-related_disorder": 1,
    "Arginase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_18|Arginase_deficiency": 1,
    "not_provided|Arginase_deficiency|ARG1-related_disorder": 3,
    "Inborn_genetic_diseases|Arginase_deficiency": 5,
    "Arginase_deficiency|Inborn_genetic_diseases": 2,
    "Arginase_deficiency|not_specified|not_provided": 1,
    "ARG1-related_disorder|Arginase_deficiency": 1,
    "not_specified|Arginase_deficiency": 4,
    "not_provided|not_specified|Arginase_deficiency": 1,
    "not_specified|Arginase_deficiency|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Arginase_deficiency": 1,
    "ARG1-related_disorder|not_provided|Arginase_deficiency": 1,
    "MED23-related_disorder|not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_18": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_18": 2,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_18": 1,
    "Intellectual_disability|_autosomal_recessive_18": 18,
    "Intellectual_disability|_autosomal_recessive_18|Inborn_genetic_diseases": 3,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_18": 1,
    "Intellectual_disability|_autosomal_recessive_18|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|MED23-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_18|MED23-related_disorder": 1,
    "MED23-related_disorder": 5,
    "MED23-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MED23-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_18|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_18": 1,
    "not_provided|MED23-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_18": 1,
    "MED23-related_disorder|Inborn_genetic_diseases": 1,
    "ENPP1-related_disorder|not_provided|Hypophosphatemic_Rickets|_Recessive|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "not_provided|ENPP1-related_disorder|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1": 3,
    "not_specified|not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1": 48,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1": 72,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 53,
    "not_provided|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 6,
    "not_provided|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1": 6,
    "ENPP1-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|Inherited_obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2": 4,
    "Inborn_genetic_diseases|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|Type_2_diabetes_mellitus": 1,
    "not_provided|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus": 2,
    "not_provided|Inborn_genetic_diseases|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus": 4,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|not_provided": 5,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|not_provided": 2,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2": 7,
    "not_provided|ENPP1-related_disorder": 5,
    "Arterial_calcification|_generalized|_of_infancy|_1": 24,
    "Inherited_obesity|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|not_provided": 2,
    "ENPP1-related_disorder": 4,
    "Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Obesity|not_provided|ENPP1-related_disorder": 2,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_Rickets|_Recessive|not_provided": 5,
    "not_specified|Hypophosphatemic_Rickets|_Recessive|not_provided|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "Hypophosphatemic_Rickets|_Recessive|not_provided|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "not_specified|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_Rickets|_Recessive|not_provided": 2,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Type_2_diabetes_mellitus|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Obesity|not_provided": 2,
    "Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Obesity": 1,
    "not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1": 13,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided": 6,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Inborn_genetic_diseases|not_provided": 1,
    "Inherited_obesity|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Intellectual_disability": 1,
    "not_provided|Inherited_obesity|Type_2_diabetes_mellitus|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1": 5,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|Inherited_obesity": 1,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome": 4,
    "ENPP1-related_disorder|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "Hypophosphatemic_rickets|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|ENPP1-related_disorder|not_specified|Diabetes_mellitus_type_2|_susceptibility_to|not_provided|Obesity|Insulin_resistance|_susceptibility_to": 1,
    "not_provided|ENPP1-related_disorder|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "not_provided|Inborn_genetic_diseases|ENPP1-related_disorder": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided|Arterial_calcification|_generalized|_of_infancy|_1": 2,
    "not_provided|Obesity|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus": 3,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Inborn_genetic_diseases": 2,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inherited_obesity|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome": 1,
    "Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Obesity|not_provided": 2,
    "not_specified|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided": 1,
    "ENPP1-related_disorder|not_provided|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_1": 2,
    "ENPP1-related_disorder|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|not_provided": 1,
    "Coronary_sclerosis|_medial|_of_infancy|not_provided|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "not_provided|Inborn_genetic_diseases|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|Type_2_diabetes_mellitus": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 4,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "Coronary_sclerosis|_medial|_of_infancy": 1,
    "not_provided|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided": 1,
    "Inborn_genetic_diseases|Inherited_obesity|Type_2_diabetes_mellitus|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|not_provided": 1,
    "Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome": 1,
    "Inborn_genetic_diseases|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1": 5,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus|not_provided": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|not_provided": 1,
    "not_specified|not_provided|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Obesity": 1,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|not_provided": 1,
    "not_provided|Dystonia_28|_childhood-onset|Arterial_calcification|_generalized|_of_infancy|_1": 1,
    "not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Inherited_obesity": 1,
    "Hypophosphatemic_rickets|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|not_provided": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|not_provided": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Inborn_genetic_diseases": 1,
    "Hypophosphatemic_rickets|not_provided|not_specified|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "not_provided|not_specified|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "Inborn_genetic_diseases|ENPP1-related_disorder": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome": 1,
    "not_provided|not_specified|Diabetes_mellitus_type_2|_susceptibility_to|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_Rickets|_Recessive|Obesity": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_Rickets|_Recessive": 1,
    "Inborn_genetic_diseases|Inherited_obesity|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|not_specified|not_provided": 1,
    "not_provided|ENPP1-related_disorder|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Obesity|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome": 1,
    "not_provided|Inherited_obesity|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus": 1,
    "not_specified|not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Type_2_diabetes_mellitus": 1,
    "not_provided|ENPP1-related_disorder|Inborn_genetic_diseases": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "ENPP1-related_disorder|not_specified|not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|ENPP1-related_disorder|not_specified|not_provided": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|not_provided|not_specified|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "Inborn_genetic_diseases|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|Obesity": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided|not_specified": 1,
    "ENPP1-related_disorder|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided": 1,
    "ENPP1-related_disorder|not_provided|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2": 1,
    "Inborn_genetic_diseases|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Inherited_obesity|Type_2_diabetes_mellitus": 1,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus|Inherited_obesity|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided": 1,
    "Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Inherited_obesity|Type_2_diabetes_mellitus|Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|not_provided": 1,
    "Inborn_genetic_diseases|Type_2_diabetes_mellitus|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Arterial_calcification|_generalized|_of_infancy|_1|Inherited_obesity|ENPP1-related_disorder|not_provided": 1,
    "ENPP1-related_disorder|not_specified|not_provided|Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Type_2_diabetes_mellitus": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_rickets|_autosomal_recessive|_2|Hypopigmentation-punctate_palmoplantar_keratoderma_syndrome|Type_2_diabetes_mellitus|Obesity": 1,
    "Arterial_calcification|_generalized|_of_infancy|_1|Hypophosphatemic_Rickets|_Recessive": 5,
    "Hypophosphatemic_rickets|_autosomal_recessive|_2|Arterial_calcification|_generalized|_of_infancy|_1|Obesity": 1,
    "Hypophosphatemic_Rickets|_Recessive|Arterial_calcification|_generalized|_of_infancy|_1": 3,
    "Kyphomelic_dysplasia": 2,
    "Spondyloepimetaphyseal_dysplasia|_Li-Shao-Li_type": 1,
    "RECLASSIFIED_-_VNN1_POLYMORPHISM": 1,
    "Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10": 52,
    "Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|not_provided": 11,
    "Nonsyndromic_Hearing_Loss|_Dominant|Dilated_Cardiomyopathy|_Dominant": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1J": 5,
    "Dilated_cardiomyopathy_1J": 433,
    "not_provided|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype": 9,
    "Dilated_cardiomyopathy_1J|Cardiovascular_phenotype": 83,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1J": 3,
    "not_provided|Dilated_cardiomyopathy_1J": 19,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1J": 64,
    "Dilated_cardiomyopathy_1J|not_provided": 21,
    "Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1J|not_specified": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|not_provided|Dilated_cardiomyopathy_1J|not_specified": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Dilated_cardiomyopathy_1J|not_provided|Cardiovascular_phenotype": 8,
    "Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1J": 5,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1J|not_provided": 5,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10": 1,
    "not_provided|EYA4-related_disorder|Dilated_cardiomyopathy_1J": 1,
    "not_provided|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10": 3,
    "Dilated_cardiomyopathy_1J|not_specified": 5,
    "not_provided|not_specified|EYA4-related_disorder|Cardiovascular_phenotype|Hearing_impairment|Dilated_cardiomyopathy_1J": 1,
    "Cardiovascular_phenotype|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided|not_specified": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1J|EYA4-related_disorder": 1,
    "not_specified|Dilated_cardiomyopathy_1J": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10": 26,
    "Dilated_cardiomyopathy_1J|not_specified|Cardiovascular_phenotype": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|Ventricular_tachycardia|Congestive_heart_failure": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|not_provided": 4,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1J|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 1,
    "Myoepithelial_tumor|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1J|Nonsyndromic_Hearing_Loss|_Dominant|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|Autosomal_dominant_nonsyndromic_hearing_loss_10": 2,
    "Cardiovascular_phenotype|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 14,
    "not_specified|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype": 1,
    "EYA4-related_disorder|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1J": 1,
    "Cardiovascular_phenotype|not_specified|EYA4-related_disorder|Dilated_cardiomyopathy_1J": 1,
    "Cardiovascular_phenotype|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided|EYA4-related_disorder|not_specified": 1,
    "Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|not_specified": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_10|Cardiovascular_phenotype|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Dilated_cardiomyopathy_1J|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1J|not_specified|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|Cardiovascular_phenotype|not_provided": 1,
    "EYA4-related_disorder": 4,
    "EYA4-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 1,
    "Cardiovascular_phenotype|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1J|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 3,
    "Dilated_cardiomyopathy_1J|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|EYA4-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_1J": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J": 1,
    "Cardiovascular_phenotype|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10": 1,
    "not_specified|not_provided|EYA4-related_disorder|Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|not_specified": 1,
    "Dilated_cardiomyopathy_1J|Autosomal_dominant_nonsyndromic_hearing_loss_10|not_specified|EYA4-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1J": 2,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1J|EYA4-related_disorder": 1,
    "Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|EYA4-related_disorder": 1,
    "EYA4-related_disorder|Dilated_cardiomyopathy_1J": 1,
    "Dilated_cardiomyopathy_1J|Hearing_impairment": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Cardiovascular_phenotype|EYA4-related_disorder|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|Autosomal_dominant_nonsyndromic_hearing_loss_10|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|Cardiovascular_phenotype|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided|not_specified": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_10": 1,
    "EYA4-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1J|Rare_genetic_deafness|EYA4-related_disorder|Cardiovascular_phenotype": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|Dilated_cardiomyopathy_1J|not_provided": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_10|not_provided|Dilated_cardiomyopathy_1J": 1,
    "TCF21-related_disorder": 2,
    "MYB-related_disorder": 6,
    "not_provided|MYB-related_disorder": 2,
    "Joubert_syndrome_3": 155,
    "Joubert_syndrome_3|not_provided": 3,
    "Joubert_syndrome_3|not_provided|not_specified": 1,
    "AHI1-related_disorder": 5,
    "Joubert_syndrome|Joubert_syndrome_3": 52,
    "Joubert_syndrome|Inborn_genetic_diseases|Joubert_syndrome_3|not_provided": 2,
    "Joubert_syndrome_3|not_specified|Joubert_syndrome|not_provided": 1,
    "AHI1-related_disorder|not_specified|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|not_provided|Inborn_genetic_diseases|Joubert_syndrome_3": 1,
    "Joubert_syndrome|Joubert_syndrome_3|not_provided|AHI1-related_disorder": 1,
    "AHI1-related_disorder|not_specified|Joubert_syndrome_3|Intellectual_disability|Retinal_dystrophy|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome_3|Joubert_syndrome": 85,
    "Joubert_syndrome|not_specified": 11,
    "Joubert_syndrome|Inborn_genetic_diseases|Joubert_syndrome_3": 4,
    "Inborn_genetic_diseases|Joubert_syndrome": 25,
    "not_provided|Joubert_syndrome|Joubert_syndrome_3|not_specified": 2,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome": 2,
    "not_provided|Joubert_syndrome|Intellectual_disability|not_specified|Joubert_syndrome_3": 1,
    "Joubert_syndrome|not_specified|not_provided|Joubert_syndrome_3": 2,
    "Retinal_dystrophy|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Joubert_syndrome_3|not_provided": 1,
    "Joubert_syndrome_3|Joubert_syndrome|not_provided": 4,
    "not_specified|Joubert_syndrome": 11,
    "Inborn_genetic_diseases|Joubert_syndrome_3|Joubert_syndrome": 5,
    "not_specified|not_provided|Joubert_syndrome|Joubert_syndrome_3|Optic_atrophy": 1,
    "not_provided|Rod-cone_dystrophy|Joubert_syndrome_3|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_3|Joubert_syndrome": 3,
    "not_provided|Joubert_syndrome|Joubert_syndrome_3": 4,
    "Joubert_syndrome_3|Joubert_syndrome|Inborn_genetic_diseases": 8,
    "Joubert_syndrome|AHI1-related_disorder": 3,
    "not_specified|Joubert_syndrome_1|Joubert_syndrome_3|Joubert_syndrome|Retinal_dystrophy|not_provided|Rod-cone_dystrophy": 1,
    "Joubert_syndrome|Joubert_syndrome_3|not_provided": 2,
    "not_provided|Joubert_syndrome_3": 6,
    "Joubert_syndrome_3|Joubert_syndrome|not_specified|Intellectual_disability|not_provided": 1,
    "Joubert_syndrome|not_provided|Joubert_syndrome_3": 6,
    "not_specified|Joubert_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Joubert_syndrome_3": 7,
    "Joubert_syndrome_3|Joubert_syndrome|not_specified|not_provided": 1,
    "Joubert_syndrome|not_specified|Joubert_syndrome_3": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|Joubert_syndrome|Joubert_syndrome_and_related_disorders|not_provided|Joubert_syndrome_3": 1,
    "not_specified|Joubert_syndrome_3|Joubert_syndrome|not_provided": 2,
    "not_provided|Joubert_syndrome|Intellectual_disability|Retinitis_pigmentosa": 1,
    "Joubert_syndrome_3|Retinal_dystrophy|Retinitis_pigmentosa|Joubert_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_3|Joubert_syndrome|AHI1-related_disorder": 1,
    "Retinal_disorders|not_specified|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_3|AHI1-related_disorder": 1,
    "AHI1-related_disorder|Joubert_syndrome": 5,
    "not_provided|not_specified|Joubert_syndrome": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_3|not_provided|Joubert_syndrome": 3,
    "Joubert_syndrome|Optic_atrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Joubert_syndrome": 6,
    "not_specified|not_provided|Joubert_syndrome_3|Joubert_syndrome": 4,
    "not_provided|Joubert_syndrome_3|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "AHI1-related_disorder|Joubert_syndrome|Joubert_syndrome_3": 2,
    "Joubert_syndrome_1|Joubert_syndrome": 4,
    "Retinal_dystrophy|not_provided|Joubert_syndrome|AHI1-related_disorder|not_specified|Intellectual_disability": 1,
    "Joubert_syndrome_3|not_specified|not_provided": 1,
    "AHI1-related_disorder|not_provided|Joubert_syndrome|Joubert_syndrome_3": 2,
    "Retinal_dystrophy|Joubert_syndrome|Joubert_syndrome_3": 1,
    "not_provided|Joubert_syndrome_3|Joubert_syndrome": 12,
    "not_provided|not_specified|Joubert_syndrome_3|Joubert_syndrome": 1,
    "Joubert_syndrome_3|Joubert_syndrome|Retinal_dystrophy|Joubert_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_3|See_cases|Joubert_syndrome": 1,
    "Joubert_syndrome|Optic_atrophy|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_3": 2,
    "Joubert_syndrome_3|not_specified|Joubert_syndrome": 3,
    "Joubert_syndrome_3|not_provided|Joubert_syndrome": 3,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_3|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome|not_specified|not_provided|Joubert_syndrome_1|Joubert_syndrome_3": 1,
    "Retinal_dystrophy|Joubert_syndrome|Inborn_genetic_diseases|Joubert_syndrome_3": 1,
    "Joubert_syndrome_3|Inborn_genetic_diseases": 3,
    "not_provided|Joubert_syndrome_3|Joubert_syndrome|not_specified": 1,
    "not_provided|Joubert_syndrome_3|Joubert_syndrome|Retinal_dystrophy|not_specified": 1,
    "Joubert_syndrome|Retinal_dystrophy": 4,
    "Joubert_syndrome|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_3": 4,
    "Joubert_syndrome|not_provided|Joubert_syndrome_3|Retinitis_pigmentosa": 1,
    "not_provided|Joubert_syndrome|Joubert_syndrome_3|Leber_congenital_amaurosis|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Joubert_syndrome|Joubert_syndrome_3|Retinal_dystrophy": 1,
    "Joubert_syndrome_3|AHI1-related_disorder|not_provided|Joubert_syndrome_with_ocular_defect|Joubert_syndrome": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_3|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome_3|Retinitis_pigmentosa": 1,
    "Joubert_syndrome_3|Inborn_genetic_diseases|Joubert_syndrome": 4,
    "Joubert_syndrome|not_provided|Joubert_syndrome_3|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_1|Joubert_syndrome_3|Joubert_syndrome|not_specified": 1,
    "AHI1-related_disorder|Retinal_dystrophy|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome|not_provided|Joubert_syndrome_3|not_specified": 1,
    "not_provided|Joubert_syndrome_3|Rod-cone_dystrophy|Joubert_syndrome": 1,
    "Joubert_syndrome_with_ocular_defect": 3,
    "Joubert_syndrome_3|not_specified|not_provided|Joubert_syndrome": 2,
    "Joubert_syndrome|Nephronophthisis|Inborn_genetic_diseases|not_provided|Joubert_syndrome_3": 1,
    "Joubert_syndrome|not_provided|AHI1-related_disorder": 2,
    "Joubert_syndrome|Inborn_genetic_diseases|AHI1-related_disorder|Joubert_syndrome_3": 1,
    "not_provided|Joubert_syndrome|not_specified": 2,
    "Joubert_syndrome|Joubert_syndrome_3|not_specified": 2,
    "Joubert_syndrome|Joubert_syndrome_and_related_disorders|Joubert_syndrome_3": 1,
    "Joubert_syndrome|Retinal_dystrophy|Joubert_syndrome_3": 1,
    "Joubert_syndrome_3|Joubert_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome_3|Joubert_syndrome|not_provided|AHI1-related_disorder|not_specified": 1,
    "Typical_Joubert_syndrome_MRI_findings|Global_developmental_delay|Joubert_syndrome_3": 1,
    "Type_2_diabetes_mellitus|Joubert_syndrome_3|Joubert_syndrome|not_provided": 1,
    "not_specified|Joubert_syndrome|Retinal_dystrophy|not_provided|Joubert_syndrome_3": 1,
    "Joubert_syndrome_and_related_disorders|Nephronophthisis|Retinal_dystrophy|not_provided|Joubert_syndrome|Joubert_syndrome_3|Rod-cone_dystrophy": 1,
    "not_provided|Joubert_syndrome_and_related_disorders|Joubert_syndrome|Joubert_syndrome_3": 1,
    "not_specified|Joubert_syndrome_3": 1,
    "Joubert_syndrome|not_provided|Joubert_syndrome_1": 3,
    "Inborn_genetic_diseases|Joubert_syndrome_3|Joubert_syndrome|not_provided": 1,
    "not_provided|Joubert_syndrome_3|not_specified|Joubert_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Retinal_dystrophy|Joubert_syndrome_3|not_specified|Joubert_syndrome": 1,
    "not_specified|not_provided|Joubert_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|Intellectual_disability": 1,
    "AHI1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Joubert_syndrome|Joubert_syndrome_3": 1,
    "Joubert_syndrome|Joubert_syndrome_with_ocular_defect|Joubert_syndrome_3|Retinal_dystrophy|not_provided": 1,
    "Joubert_syndrome|not_specified|Inborn_genetic_diseases|not_provided|Joubert_syndrome_3": 1,
    "Joubert_syndrome_3|Joubert_syndrome|AHI1-related_disorder": 2,
    "not_provided|Joubert_syndrome_and_related_disorders|Joubert_syndrome_3|Retinal_dystrophy|Joubert_syndrome": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_3|See_cases": 1,
    "not_specified|AHI1-related_disorder|Joubert_syndrome_3|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|Retinal_dystrophy|Joubert_syndrome_3|not_provided": 1,
    "Joubert_syndrome|Joubert_syndrome_3|Joubert_syndrome_and_related_disorders": 1,
    "not_specified|Joubert_syndrome|Joubert_syndrome_3|AHI1-related_disorder|not_provided": 1,
    "Joubert_syndrome|not_provided|not_specified|Joubert_syndrome_3": 1,
    "Retinal_dystrophy|Joubert_syndrome_3|Joubert_syndrome_and_related_disorders|Joubert_syndrome": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|not_provided|Joubert_syndrome_3": 2,
    "Joubert_syndrome|not_provided|Joubert_syndrome_3|AHI1-related_disorder|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_3|Joubert_syndrome": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome_and_related_disorders|not_provided|Joubert_syndrome|Joubert_syndrome_3": 1,
    "Joubert_syndrome|not_provided|Retinal_dystrophy|Joubert_syndrome_3": 1,
    "Joubert_syndrome_3|Type_2_diabetes_mellitus|AHI1-related_disorder|Joubert_syndrome": 1,
    "AHI1-related_disorder|not_specified|not_provided": 1,
    "BCLAF1-related_disorder|not_specified": 2,
    "BCLAF1-related_disorder": 4,
    "not_specified|BCLAF1-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy": 19,
    "Peroxisome_biogenesis_disorder_9B|not_provided|Rhizomelic_chondrodysplasia_punctata_type_1": 3,
    "Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata": 2,
    "Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 7,
    "Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B|not_provided": 2,
    "Rhizomelic_chondrodysplasia_punctata|not_provided|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 2,
    "Rhizomelic_chondrodysplasia_punctata_type_1": 39,
    "Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 38,
    "not_specified|Rhizomelic_chondrodysplasia_punctata_type_1|Rhizomelic_chondrodysplasia_punctata|not_provided|Peroxisome_biogenesis_disorder_9B": 1,
    "PEX7-related_disorder": 3,
    "Rhizomelic_chondrodysplasia_punctata|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "Peroxisome_biogenesis_disorder_9B": 397,
    "Peroxisome_biogenesis_disorder_9B|not_provided": 5,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|Inborn_genetic_diseases": 1,
    "not_specified|Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder|Inborn_genetic_diseases|not_provided|Rhizomelic_chondrodysplasia_punctata": 1,
    "Peroxisome_biogenesis_disorder_9B|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B": 5,
    "PEX7-related_disorder|Peroxisome_biogenesis_disorder_9B": 7,
    "Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder|not_provided": 2,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B": 11,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata_type_1|Rhizomelic_chondrodysplasia_punctata|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata|not_provided|Peroxisome_biogenesis_disorder_9B|Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|not_specified": 1,
    "PEX7-related_disorder|Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B": 1,
    "not_specified|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 2,
    "PEX7-related_disorder|Rhizomelic_chondrodysplasia_punctata|Phytanic_acid_storage_disease|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_1|Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_1|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_9B|Connective_tissue_disorder|PEX7-related_disorder": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata_type_1|PEX7-related_disorder": 1,
    "not_provided|PEX7-related_disorder|Peroxisome_biogenesis_disorder_9B": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|not_provided": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata|not_provided": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 4,
    "Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata_type_1|not_provided": 1,
    "PEX7-related_disorder|not_specified|not_provided|Peroxisome_biogenesis_disorder_9B|Intellectual_disability|Peroxisome_biogenesis_disorder|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B": 7,
    "Rhizomelic_chondrodysplasia_punctata_type_1|not_specified": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata": 8,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata|Rhizomelic_chondrodysplasia_punctata_type_1|Connective_tissue_disorder|Phytanic_acid_storage_disease": 1,
    "Rhizomelic_chondrodysplasia_punctata|PEX7-related_disorder|Peroxisome_biogenesis_disorder_9B": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B|not_provided|Rhizomelic_chondrodysplasia_punctata_type_1|Phytanic_acid_storage_disease": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 6,
    "not_provided|Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_1|PEX7-related_disorder|Peroxisome_biogenesis_disorder_9B": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata": 1,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "not_provided|not_specified|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "Inborn_genetic_diseases|not_provided|Retinal_dystrophy|Peroxisome_biogenesis_disorder_9B|Peroxisome_biogenesis_disorder|Rhizomelic_chondrodysplasia_punctata_type_1|Phytanic_acid_storage_disease": 1,
    "Rhizomelic_chondrodysplasia_punctata|Connective_tissue_disorder|Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata_type_1|not_specified|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease": 1,
    "not_specified|Peroxisome_biogenesis_disorder_9B": 2,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|PEX7-related_disorder|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder": 3,
    "not_specified|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_9B": 1,
    "Intermediate_form_of_PEX7_related_rhizomelic_chondrodysplasia_punctata": 1,
    "Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|Phytanic_acid_storage_disease": 1,
    "PEX7-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "not_specified|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata|PEX7-related_disorder|Phytanic_acid_storage_disease|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|not_provided": 1,
    "Peroxisome_biogenesis_disorder_9B|Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata_type_1|PEX7-related_disorder|not_provided": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata": 1,
    "Connective_tissue_disorder|not_specified|Peroxisome_biogenesis_disorder_9B": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|not_specified": 1,
    "not_provided|Rhizomelic_chondrodysplasia_punctata_type_1|Phytanic_acid_storage_disease|Peroxisome_biogenesis_disorder_9B|Retinal_dystrophy": 1,
    "Rhizomelic_chondrodysplasia_punctata|Peroxisome_biogenesis_disorder_9B|not_provided": 1,
    "Peroxisome_biogenesis_disorder_9B|Inborn_genetic_diseases|not_provided|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B|PEX7-related_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|Inborn_genetic_diseases": 1,
    "PEX7-related_disorder|not_specified|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "PEX7-related_disorder|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata_type_1|Phytanic_acid_storage_disease|not_provided": 1,
    "PEX7-related_disorder|Rhizomelic_chondrodysplasia_punctata|not_provided|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "Peroxisome_biogenesis_disorder_9B|not_specified|not_provided": 1,
    "PEX7-related_disorder|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "Phytanic_acid_storage_disease|Rhizomelic_chondrodysplasia_punctata_type_1|Peroxisome_biogenesis_disorder_9B": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "Peroxisome_biogenesis_disorder_9B|Connective_tissue_disorder|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "Rhizomelic_chondrodysplasia_punctata|Phytanic_acid_storage_disease|not_provided": 1,
    "Rhizomelic_chondrodysplasia_punctata|Phytanic_acid_storage_disease": 1,
    "not_provided|Peroxisome_biogenesis_disorder_9B|Rhizomelic_chondrodysplasia_punctata|Rhizomelic_chondrodysplasia_punctata_type_1": 1,
    "Immunodeficiency_27A": 41,
    "not_provided|Immunodeficiency_27A": 1,
    "Immunodeficiency_27A|not_provided": 1,
    "Disseminated_atypical_mycobacterial_infection": 240,
    "Disseminated_atypical_mycobacterial_infection|Immunodeficiency_27A": 11,
    "Disseminated_atypical_mycobacterial_infection|not_specified": 4,
    "not_specified|Immunodeficiency_27A|Disseminated_atypical_mycobacterial_infection|not_provided": 2,
    "Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency": 4,
    "not_provided|Disseminated_atypical_mycobacterial_infection": 11,
    "Immunodeficiency_27A|Helicobacter_pylori_infection|_susceptibility_to|Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|Disseminated_atypical_mycobacterial_infection|IFNGR1-related_disorder|not_provided|not_specified": 1,
    "Immunodeficiency_27A|Disseminated_atypical_mycobacterial_infection": 4,
    "Disseminated_atypical_mycobacterial_infection|Inborn_genetic_diseases": 4,
    "Disseminated_atypical_mycobacterial_infection|not_provided": 5,
    "Disseminated_atypical_mycobacterial_infection|IFNGR1-related_disorder|not_specified|Immunodeficiency_27A": 1,
    "Inborn_genetic_diseases|Disseminated_atypical_mycobacterial_infection": 4,
    "IFNGR1-related_disorder|Disseminated_atypical_mycobacterial_infection|not_provided": 1,
    "Disseminated_atypical_mycobacterial_infection|not_specified|not_provided|Immunodeficiency_27A": 1,
    "Immunodeficiency_27A|not_provided|Disseminated_atypical_mycobacterial_infection": 2,
    "not_provided|Disseminated_atypical_mycobacterial_infection|Immunodeficiency_27A|Hepatitis_B_virus|_susceptibility_to|Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|Mycobacterium_tuberculosis|_susceptibility_to|Helicobacter_pylori_infection|_susceptibility_to|Interferon_gamma_receptor_deficiency": 1,
    "Disseminated_atypical_mycobacterial_infection|Helicobacter_pylori_infection|_susceptibility_to|Hepatitis_B_virus|_susceptibility_to|Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|Mycobacterium_tuberculosis|_susceptibility_to|Immunodeficiency_27A": 1,
    "Disseminated_atypical_mycobacterial_infection|not_specified|Immunodeficiency_27A": 2,
    "Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|not_provided|Disseminated_atypical_mycobacterial_infection|IFN-gamma_receptor_1_deficiency|Helicobacter_pylori_infection|_susceptibility_to|Immunodeficiency_27A|Hepatitis_B_virus|_susceptibility_to|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "Disseminated_atypical_mycobacterial_infection|IFNGR1-related_disorder": 1,
    "Immunodeficiency_27A|Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|Disseminated_atypical_mycobacterial_infection|Hepatitis_B_virus|_susceptibility_to|Helicobacter_pylori_infection|_susceptibility_to|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "Immunodeficiency_27A|not_specified|Disseminated_atypical_mycobacterial_infection": 1,
    "Hepatitis_B_virus|_susceptibility_to|Helicobacter_pylori_infection|_susceptibility_to|Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|Immunodeficiency_27A|Mycobacterium_tuberculosis|_susceptibility_to|Disseminated_atypical_mycobacterial_infection": 1,
    "IFNGR1-related_disorder|Immunodeficiency_27A|not_specified|Disseminated_atypical_mycobacterial_infection|not_provided": 1,
    "Disseminated_atypical_mycobacterial_infection|Immunodeficiency_27A|Inherited_Immunodeficiency_Diseases|not_provided": 1,
    "Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|Helicobacter_pylori_infection|_susceptibility_to|Immunodeficiency_27A|Inborn_genetic_diseases|IFNGR1-related_disorder|Disseminated_atypical_mycobacterial_infection": 1,
    "Disseminated_atypical_mycobacterial_infection|Immunodeficiency_27A|not_provided|Interferon_gamma_receptor_deficiency": 1,
    "Immunodeficiency_27A|Mycobacterium_tuberculosis|_susceptibility_to|Disseminated_atypical_mycobacterial_infection|not_provided": 1,
    "Disseminated_atypical_mycobacterial_infection|not_specified|IFNGR1-related_disorder": 1,
    "Disseminated_atypical_mycobacterial_infection|Interferon_gamma_receptor_deficiency": 1,
    "Disseminated_atypical_mycobacterial_infection|Immunodeficiency_27A|IFNGR1-related_disorder": 1,
    "IFNGR1-related_disorder": 1,
    "Disseminated_atypical_mycobacterial_infection|not_specified|Autosomal_dominant_mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IFNgammaR1_deficiency|not_provided|Immunodeficiency_27A": 1,
    "IFNGR1-related_disorder|Disseminated_atypical_mycobacterial_infection": 1,
    "Disseminated_atypical_mycobacterial_infection|IFNGR1-related_disorder|not_provided|Interferon_gamma_receptor_deficiency|Immunodeficiency_27A": 1,
    "Mycobacterium_tuberculosis|_protection_against|Disseminated_atypical_mycobacterial_infection|Immunodeficiency_27A|Hepatitis_B_virus|_susceptibility_to|Helicobacter_pylori_infection|_susceptibility_to|not_specified": 1,
    "Autoinflammatory_syndrome|_familial|_Behcet-like": 5,
    "Autoinflammatory_syndrome|_familial|_Behcet-like_1": 25,
    "Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_provided": 12,
    "Autoinflammatory_syndrome|_familial|_Behcet-like|not_provided": 4,
    "not_provided|Autoinflammatory_syndrome|_familial|_Behcet-like_1": 11,
    "TNFAIP3-related_disorder|Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_provided": 1,
    "not_provided|not_specified|Autoinflammatory_syndrome|_familial|_Behcet-like_1": 1,
    "not_specified|not_provided|Autoinflammatory_syndrome|_familial|_Behcet-like_1|Autoinflammatory_syndrome|_familial|_Behcet-like": 1,
    "Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_provided|not_specified": 2,
    "A20_haploinsufficiency|Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_specified|not_provided": 1,
    "not_specified|not_provided|Autoinflammatory_syndrome|_familial|_Behcet-like_1": 1,
    "TNFAIP3-related_disorder|not_provided": 5,
    "Autoinflammatory_syndrome|_familial|_Behcet-like_1|A20_haploinsufficiency|not_specified|not_provided": 1,
    "TNFAIP3-related_disorder|not_specified": 1,
    "not_provided|not_specified|Autoinflammatory_syndrome|_familial|_Behcet-like": 2,
    "not_provided|Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_specified": 1,
    "TNFAIP3-related_disorder": 5,
    "Autoinflammatory_syndrome|_familial|_Behcet-like|Inborn_genetic_diseases": 2,
    "Autoinflammatory_syndrome|_familial|_Behcet-like_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autoinflammatory_syndrome|_familial|_Behcet-like_1": 2,
    "Inborn_genetic_diseases|not_provided|Autoinflammatory_syndrome|_familial|_Behcet-like": 1,
    "not_provided|Autoinflammatory_syndrome|_familial|_Behcet-like": 2,
    "TNFAIP3-related_disorder|Autoinflammatory_syndrome|_familial|_Behcet-like|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|TNFAIP3-related_disorder|not_provided": 1,
    "not_provided|TNFAIP3-related_disorder": 3,
    "not_provided|not_specified|TNFAIP3-related_disorder": 1,
    "Autoinflammatory_syndrome|_familial|_Behcet-like|Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_specified|not_provided": 1,
    "TNFAIP3-related_disorder|Autoinflammatory_syndrome|_familial|_Behcet-like|not_provided": 1,
    "Autoinflammatory_syndrome|_familial|_Behcet-like_1|TNFAIP3-related_disorder|not_specified|not_provided": 1,
    "not_provided|TNFAIP3-related_disorder|Inborn_genetic_diseases": 1,
    "TNFAIP3-related_disorder|Autoinflammatory_syndrome|_familial|_Behcet-like_1|not_specified|not_provided": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_7": 1,
    "Olmsted_syndrome_2": 4,
    "not_provided|PERP-related_disorder": 1,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_7": 1,
    "ARFGEF3-related_disorder": 37,
    "not_specified|ARFGEF3-related_disorder": 1,
    "ARFGEF3-related_disorder|not_provided": 7,
    "not_specified|not_provided|ARFGEF3-related_disorder": 1,
    "not_provided|ARFGEF3-related_disorder": 2,
    "ARFGEF3-related_disorder|not_specified": 2,
    "REPS1-related_disorder|Neurodegeneration_with_brain_iron_accumulation_7|not_provided": 1,
    "not_provided|REPS1-related_disorder": 5,
    "Neurodegeneration_with_brain_iron_accumulation_7|not_specified|not_provided": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_7": 1,
    "REPS1-related_disorder": 1,
    "REPS1-related_disorder|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation_7|not_provided|Neurodegeneration_with_brain_iron_accumulation": 1,
    "Neurodegeneration_with_brain_iron_accumulation_7": 1,
    "Atrial_septal_defect_8": 3,
    "Ventricular_septal_defect_2": 2,
    "not_provided|Ventricular_septal_defect_2|Atrial_septal_defect_8": 1,
    "CITED2-related_disorder|not_provided": 1,
    "not_provided|CITED2-related_disorder": 2,
    "CITED2-related_disorder|not_specified": 1,
    "CITED2-related_disorder": 5,
    "Ventricular_septal_defect_2|CITED2-related_disorder": 1,
    "not_provided|Ventricular_septal_defect_2": 1,
    "not_specified|CITED2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|CITED2-related_disorder": 2,
    "CITED2-related_disorder|not_specified|not_provided|Atrial_septal_defect_8": 1,
    "Lethal_congenital_contracture_syndrome_9|Arthrogryposis_multiplex_congenita": 3,
    "not_provided|Inborn_genetic_diseases|ADGRG6-related_disorder": 1,
    "not_provided|Lethal_congenital_contracture_syndrome_9": 1,
    "Lethal_congenital_contracture_syndrome_9": 9,
    "not_provided|ADGRG6-related_disorder": 3,
    "ADGRG6-related_disorder": 6,
    "ADGRG6-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_43|not_provided": 14,
    "not_provided|Intellectual_disability|_autosomal_dominant_43": 18,
    "HIVEP2-related_disorder": 24,
    "not_provided|HIVEP2-related_disorder": 26,
    "Intellectual_disability|_autosomal_dominant_43": 101,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_43|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_43": 4,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_43": 5,
    "Intellectual_disability|not_provided|Epilepsy|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_43|not_provided|not_specified": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_43|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_43": 1,
    "HIVEP2-related_disorder|not_provided": 18,
    "not_provided|Congenital_ocular_coloboma|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_43|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_43": 3,
    "HIVEP2-related_disorder|not_provided|not_specified": 2,
    "not_provided|Angelman_syndrome-like|Intellectual_disability|_autosomal_dominant_43": 1,
    "not_provided|HIVEP2-related_disorder|not_specified": 2,
    "HIVEP2-related_syndromic_intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_43|not_provided|HIVEP2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|HIVEP2-related_disorder": 2,
    "Intellectual_disability|_autosomal_dominant_43|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|HIVEP2-related_disorder|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_43|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|HIVEP2-related_disorder": 3,
    "not_provided|Intellectual_disability|_autosomal_dominant_43|Inborn_genetic_diseases": 2,
    "HIVEP2-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|HIVEP2-related_disorder": 1,
    "HIVEP2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Angelman_syndrome-like": 1,
    "Intellectual_disability|_autosomal_dominant_43|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_43|not_provided|Inborn_genetic_diseases": 3,
    "Intellectual_disability|_autosomal_dominant_13": 68,
    "Vascular_disorder": 3,
    "not_provided|HIVEP2-related_disorder|Intellectual_disability|_autosomal_dominant_43": 1,
    "not_specified|HIVEP2-related_disorder|not_provided": 1,
    "See_cases|HIVEP2-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_10A_(Zellweger)": 36,
    "not_provided|Peroxisome_biogenesis_disorder_10A_(Zellweger)": 12,
    "Peroxisome_biogenesis_disorder_10A_(Zellweger)|Peroxisome_biogenesis_disorder_10B": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_10A_(Zellweger)": 3,
    "Peroxisome_biogenesis_disorder_10B": 2,
    "PEX3-related_disorder": 2,
    "not_provided|PEX3-related_disorder": 5,
    "not_provided|PEX3-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_10B|not_specified|not_provided|Peroxisome_biogenesis_disorder_10A_(Zellweger)": 1,
    "PEX3-related_disorder|not_provided": 3,
    "not_provided|Peroxisome_biogenesis_disorder_10A_(Zellweger)|PEX3-related_disorder": 2,
    "Peroxisome_biogenesis_disorder_10A_(Zellweger)|not_provided": 1,
    "not_specified|PEX3-related_disorder|not_provided": 1,
    "not_specified|Peroxisome_biogenesis_disorder_10B|Peroxisome_biogenesis_disorder_10A_(Zellweger)|not_provided": 1,
    "not_provided|PEX3-related_disorder|Peroxisome_biogenesis_disorder_10A_(Zellweger)|Peroxisome_biogenesis_disorder_10B": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_10A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_10A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_10B|not_provided": 1,
    "High_myopia|not_specified": 3,
    "Inflammatory_poikiloderma_with_hair_abnormalities_and_acral_keratoses": 1,
    "PLAGL1-related_disorder": 3,
    "PLAGL1-related_disorder|not_provided": 2,
    "not_provided|PLAGL1-related_disorder": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_4": 334,
    "Familial_hemophagocytic_lymphohistiocytosis": 30,
    "Familial_hemophagocytic_lymphohistiocytosis_4|Inborn_genetic_diseases|not_provided": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_4": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_4|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_4|Inborn_genetic_diseases": 4,
    "Familial_hemophagocytic_lymphohistiocytosis_4|not_specified|STX11-related_disorder": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_4": 9,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_4": 4,
    "Familial_hemophagocytic_lymphohistiocytosis_4|not_provided": 4,
    "Autoinflammatory_syndrome|not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_4": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|not_provided|Familial_hemophagocytic_lymphohistiocytosis_4": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_4|Autoinflammatory_syndrome|STX11-related_disorder": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_4|STX11-related_disorder": 2,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_4|not_specified": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_4|not_provided": 1,
    "STX11-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_4": 2,
    "not_provided|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_4|not_specified": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_4|not_provided|Autoinflammatory_syndrome|STX11-related_disorder": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|not_specified|Familial_hemophagocytic_lymphohistiocytosis_4|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_4": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_4|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_4|not_specified": 1,
    "Duchenne_muscular_dystrophy": 4428,
    "EPM2A-related_disorder": 1,
    "Cataract|Severe_global_developmental_delay|Microcephaly": 1,
    "Progressive_myoclonic_epilepsy|Lafora_disease": 11,
    "Myoclonic_epilepsy_of_Lafora_1|Lafora_disease": 3,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided": 8,
    "not_specified|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 2,
    "not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_specified": 1,
    "Lafora_disease|Progressive_myoclonic_epilepsy": 3,
    "Myoclonic_epilepsy_of_Lafora_1|Progressive_myoclonic_epilepsy|not_provided|Lafora_disease": 3,
    "Progressive_myoclonic_epilepsy|not_specified|not_provided": 2,
    "Progressive_myoclonic_epilepsy|not_provided|not_specified": 1,
    "Lafora_disease|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Lafora_disease|Progressive_myoclonic_epilepsy": 1,
    "not_specified|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|EPM2A-related_disorder": 1,
    "Lafora_disease|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 1,
    "Progressive_myoclonic_epilepsy|Lafora_disease|not_provided": 1,
    "Progressive_myoclonic_epilepsy|not_specified|EPM2A-related_disorder": 1,
    "Progressive_myoclonic_epilepsy|not_specified|Seizure|Myoclonic_epilepsy_of_Lafora_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Lafora_disease|Myoclonic_epilepsy_of_Lafora_1|EPM2A-related_disorder|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Myoclonic_epilepsy_of_Lafora_1|EPM2A-related_disorder|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_provided|Lafora_disease": 1,
    "Inborn_genetic_diseases|not_specified|Progressive_myoclonic_epilepsy|not_provided": 2,
    "Progressive_myoclonic_epilepsy|EPM2A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 5,
    "EPM2A-related_disorder|not_specified|Intellectual_disability|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Myoclonic_epilepsy_of_Lafora_1|Progressive_myoclonic_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Lafora_disease": 1,
    "EPM2A-related_disorder|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|Intellectual_disability": 1,
    "Lafora_disease|Progressive_myoclonic_epilepsy|Myoclonic_epilepsy|_progressive|_X-linked": 1,
    "Progressive_myoclonic_epilepsy|not_provided|Lafora_disease": 1,
    "not_provided|Progressive_myoclonic_epilepsy|Lafora_disease|Inborn_genetic_diseases": 1,
    "Lafora_disease|Progressive_myoclonic_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Lafora_disease|not_specified|not_provided": 1,
    "EPM2A-related_disorder|Inborn_genetic_diseases|not_specified|Progressive_myoclonic_epilepsy|not_provided|Cataract|Microcephaly|Severe_global_developmental_delay": 1,
    "Myoclonic_epilepsy_of_Lafora_1|Progressive_myoclonic_epilepsy|Lafora_disease": 2,
    "not_provided|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 8,
    "not_specified|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 1,
    "Lafora_disease|not_provided|Progressive_myoclonic_epilepsy": 1,
    "not_provided|Myoclonic_epilepsy_of_Lafora_1|Lafora_disease": 1,
    "Inborn_genetic_diseases|not_provided|EPM2A-related_disorder|Lafora_disease|Progressive_myoclonic_epilepsy": 1,
    "Myoclonic_epilepsy_of_Lafora_1|Progressive_myoclonic_epilepsy": 1,
    "not_provided|Myoclonic_epilepsy_of_Lafora_1": 1,
    "not_provided|Lafora_disease|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_specified|Progressive_myoclonic_epilepsy": 2,
    "Lafora_disease|Myoclonic_epilepsy_of_Lafora_1|not_provided": 1,
    "Progressive_myoclonic_epilepsy|Myoclonic_epilepsy_of_Lafora_1|Lafora_disease|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_specified|not_provided|Lafora_disease": 2,
    "Lafora_disease|Progressive_myoclonic_epilepsy|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy": 2,
    "Inborn_genetic_diseases|Lafora_disease|Myoclonic_epilepsy_of_Lafora_1|Progressive_myoclonic_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Lafora_disease|Myoclonic_epilepsy_of_Lafora_1|EPM2A-related_disorder|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|EPM2A-related_disorder": 1,
    "Inborn_genetic_diseases|EPM2A-related_disorder|Progressive_myoclonic_epilepsy": 1,
    "not_provided|Progressive_myoclonic_epilepsy|Lafora_disease": 1,
    "Lafora_disease|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|not_specified|Lafora_disease": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_13|not_provided": 2,
    "Spinocerebellar_ataxia_44": 7,
    "not_provided|Spinocerebellar_ataxia_44|Autosomal_recessive_spinocerebellar_ataxia_13": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44|not_provided": 1,
    "GRM1-related_disorder|not_provided": 4,
    "Autosomal_recessive_spinocerebellar_ataxia_13|Global_developmental_delay": 1,
    "GRM1-related_disorder|not_specified|not_provided": 3,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_13": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44": 2,
    "Spinocerebellar_ataxia_44|Autosomal_recessive_spinocerebellar_ataxia_13|Cerebellar_ataxia|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_13": 4,
    "not_provided|Spinocerebellar_ataxia_44": 1,
    "not_provided|GRM1-related_disorder": 2,
    "Spinocerebellar_ataxia_44|Autosomal_recessive_spinocerebellar_ataxia_13|not_specified|not_provided": 3,
    "Spinocerebellar_ataxia_44|not_provided": 1,
    "Spinocerebellar_ataxia_44|Autosomal_recessive_spinocerebellar_ataxia_13|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_13|not_specified|not_provided|Spinocerebellar_ataxia_44": 1,
    "GRM1-related_disorder": 1,
    "not_specified|GRM1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44|not_specified": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_44|Autosomal_recessive_spinocerebellar_ataxia_13": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44|not_provided|not_specified": 1,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_13|Spinocerebellar_ataxia_44|not_provided": 1,
    "STXBP5-related_disorder": 22,
    "STXBP5-related_disorder|not_provided": 6,
    "not_provided|STXBP5-related_disorder": 1,
    "not_provided|Cancer|_alopecia|_pigment_dyscrasia|_onychodystrophy|_and_keratoderma|Dyschromatosis_universalis_hereditaria_1": 2,
    "SASH1-related_disorder": 22,
    "not_provided|SASH1-related_disorder": 8,
    "Dyschromatosis_universalis_hereditaria_1|not_provided|Cancer|_alopecia|_pigment_dyscrasia|_onychodystrophy|_and_keratoderma": 2,
    "Wilson_disease": 2457,
    "Dyschromatosis_universalis_hereditaria_1": 14,
    "not_provided|Dyschromatosis_universalis_hereditaria_1": 1,
    "Wilson_disease|Developmental_and_epileptic_encephalopathy|_13": 1,
    "SASH1-related_disorder|not_provided": 1,
    "dyschromatosis|Ungual_dystrophy|spino-cellular_carcinoma|Alopecia|Palmoplantar_keratoderma|Cancer|_alopecia|_pigment_dyscrasia|_onychodystrophy|_and_keratoderma": 1,
    "SASH1-related_disorder|Inborn_genetic_diseases": 1,
    "Dyschromatosis_universalis_hereditaria_1|Cancer|_alopecia|_pigment_dyscrasia|_onychodystrophy|_and_keratoderma": 2,
    "Dyschromatosis_universalis_hereditaria_1|Cancer|_alopecia|_pigment_dyscrasia|_onychodystrophy|_and_keratoderma|not_provided|not_specified": 1,
    "not_specified|not_provided|SASH1-related_disorder": 1,
    "Cancer|_alopecia|_pigment_dyscrasia|_onychodystrophy|_and_keratoderma|Dyschromatosis_universalis_hereditaria_1": 1,
    "Congenital_heart_defects|_multiple_types|_2": 36,
    "not_provided|Congenital_heart_defects|_multiple_types|_2": 6,
    "TAB2-related_disorder": 8,
    "not_provided|TAB2-related_disorder": 1,
    "TAB2-related_disorder|Inborn_genetic_diseases": 1,
    "TAB2-related_disorder|not_provided": 3,
    "TAB2-related_disorder|Inborn_genetic_diseases|Encephalopathy|Congenital_heart_defects|_multiple_types|_2|not_provided": 1,
    "TAB2-related_syndrome": 1,
    "not_specified|not_provided|Congenital_heart_defects|_multiple_types|_2|Inborn_genetic_diseases": 1,
    "Congenital_heart_defects|_multiple_types|_2|Atrial_septal_defect|_ostium_secundum_type|Stress_urinary_incontinence|Migraine|Bicuspid_aortic_valve|Rectal_prolapse|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_2|not_provided": 2,
    "TAB2-related_disorder|not_provided|Congenital_heart_defects|_multiple_types|_2": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Congenital_heart_defects|_multiple_types|_2": 1,
    "Inborn_genetic_diseases|TAB2-related_disorder": 1,
    "Congenital_heart_defects|_multiple_types|_2|TAB2-related_disorder": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_2|Polyvalvular_heart_disease_syndrome": 1,
    "not_specified|not_provided|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_5": 1,
    "IYD-related_disorder|not_provided": 1,
    "IYD-related_disorder": 3,
    "not_provided|IYD-related_disorder": 5,
    "Iodotyrosine_deiodination_defect": 7,
    "Iodotyrosine_deiodination_defect|IYD-related_disorder": 1,
    "IYD-related_disorder|Iodotyrosine_deiodination_defect|not_specified": 1,
    "Iodotyrosine_deiodination_defect|not_provided": 1,
    "not_specified|IYD-related_disorder|not_provided": 1,
    "Iodotyrosine_deiodination_defect|not_specified": 1,
    "not_specified|not_provided|Iodotyrosine_deiodination_defect": 1,
    "Congenital_hypothyroidism|not_provided": 5,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_11|Mitochondrial_disease": 1,
    "Combined_oxidative_phosphorylation_defect_type_11": 53,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_11": 15,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_11": 2,
    "Combined_oxidative_phosphorylation_defect_type_11|not_provided": 9,
    "Combined_oxidative_phosphorylation_defect_type_11|Inborn_genetic_diseases|not_provided": 4,
    "Combined_oxidative_phosphorylation_defect_type_11|Mitochondrial_disease|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|Inborn_genetic_diseases": 6,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_11|Inborn_genetic_diseases": 2,
    "not_provided|RMND1-related_disorder|Combined_oxidative_phosphorylation_defect_type_11": 2,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_11": 2,
    "Autosomal_recessive_Combined_oxidative_phosphorylation_deficiency_11": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|RMND1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_11|not_provided": 1,
    "not_provided|RMND1-related_disorder": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_11": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|not_provided|RMND1-related_disorder|Inborn_genetic_diseases": 1,
    "RMND1-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|not_provided|RMND1-related_disorder|not_specified": 1,
    "RMND1-related_disorder": 1,
    "Mitochondrial_oxidative_phosphorylation_disorder|Nephronophthisis|Inborn_genetic_diseases|Mitochondrial_disease|not_provided|Combined_oxidative_phosphorylation_defect_type_11": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_11|not_specified": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|not_specified|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|Mitochondrial_disease": 1,
    "Combined_oxidative_phosphorylation_defect_type_11|Abnormality_of_the_nervous_system": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_11": 3,
    "Combined_oxidative_phosphorylation_defect_type_11|not_provided|not_specified": 1,
    "Estrogen_resistance_syndrome|not_specified|CCDC170-related_condition": 1,
    "not_specified|Estrogen_resistance_syndrome": 1,
    "not_provided|ESR1-related_disorder": 1,
    "ESR1-related_disorder": 3,
    "not_provided|Myocardial_infarction|_susceptibility_to|Estrogen_resistance_syndrome|Migraine_with_or_without_aura|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "ESR1-related_disorder|not_provided": 5,
    "Familial_cancer_of_breast|Migraine_with_or_without_aura|_susceptibility_to|_1|Estrogen_resistance_syndrome": 2,
    "Estrogen_receptor_mutant|_temperature-sensitive": 1,
    "Migraine_with_or_without_aura|_susceptibility_to|not_provided|ESR1-related_disorder|Estrogen_resistance_syndrome|Migraine_with_or_without_aura|_susceptibility_to|_1|Familial_cancer_of_breast|Myocardial_infarction|_susceptibility_to": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1538,
    "Cerebellar_ataxia|Emery-Dreifuss_muscular_dystrophy": 3,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1171,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 327,
    "Autosomal_recessive_ataxia|_Beauce_type|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 10,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 206,
    "Rare_genetic_intellectual_disability|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided": 36,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 284,
    "Cleft_lip/palate|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 53,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 44,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 20,
    "not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Abnormality_of_the_musculature": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 5,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 28,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 7,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder|not_provided|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_provided|SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 2,
    "not_provided|SYNE1-related_disorder": 5,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type": 6,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 6,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 22,
    "SYNE1-related_disorder|Inborn_genetic_diseases|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type": 12,
    "SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 4,
    "SYNE1-related_disorder|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Autosomal_recessive_ataxia|_Beauce_type": 5,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|not_specified": 12,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 191,
    "not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 25,
    "not_provided|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 3,
    "SYNE1-related_disorder|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 2,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Intellectual_disability": 1,
    "Spastic_ataxia|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 7,
    "Autosomal_recessive_ataxia|_Beauce_type": 87,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified": 36,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|SYNE1-related_disorder|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified": 2,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 20,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Intellectual_disability": 1,
    "Emery-Dreifuss_muscular_dystrophy|Cerebellar_ataxia": 3,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided": 1,
    "SYNE1-related_disorder": 42,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 13,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 2,
    "Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 5,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified": 9,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type": 8,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 3,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder": 5,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder": 4,
    "SYNE1-related_disorder|Intellectual_disability|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified": 13,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder": 5,
    "not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|SYNE1-related_disorder": 1,
    "Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 7,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided": 1,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 11,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_provided|Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|SYNE1-related_disorder": 7,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder|not_provided": 2,
    "SYNE1-related_disorder|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 5,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 16,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 3,
    "Autosomal_recessive_ataxia|_Beauce_type|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 2,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 2,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 4,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified|Intellectual_disability": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 10,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Hereditary_ataxia": 1,
    "not_provided|Juvenile_amyotrophic_lateral_sclerosis": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|SYNE1-related_disorder": 1,
    "Inborn_genetic_diseases|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_specified|not_provided": 8,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|not_provided": 5,
    "SYNE1-related_disorder|not_provided": 5,
    "Autosomal_recessive_ataxia|_Beauce_type|not_provided": 4,
    "SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 8,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder": 4,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_provided": 4,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Autosomal_recessive_ataxia|_Beauce_type": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 4,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 7,
    "Neurodevelopmental_abnormality|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy|Cerebellar_ataxia": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_provided|Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 6,
    "Cerebellar_ataxia|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Emery-Dreifuss_muscular_dystrophy": 3,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Emery-Dreifuss_muscular_dystrophy|Cerebellar_ataxia": 1,
    "not_specified|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "not_provided|SYNE1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases": 3,
    "Abnormal_central_motor_function|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Autosomal_recessive_myogenic_arthrogryposis_multiplex_congenita|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder|not_specified|not_provided": 1,
    "Shoulder_girdle_muscle_weakness|EMG:_myopathic_abnormalities": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Abnormal_brain_morphology": 1,
    "SYNE1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified|not_provided|SYNE1-related_disorder": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "not_specified|See_cases|not_provided|Intellectual_disability": 1,
    "not_specified|SYNE1-related_disorder|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|SYNE1-related_disorder": 4,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|Limb-girdle_muscular_dystrophy|not_provided|Intellectual_disability": 1,
    "SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Intellectual_disability": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Autosomal_recessive_ataxia|_Beauce_type": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified": 2,
    "not_specified|not_provided|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_specified|Cerebellar_ataxia|Emery-Dreifuss_muscular_dystrophy|SYNE1-related_disorder|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided": 5,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type": 2,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided": 2,
    "SYNE1-related_disorder|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Intellectual_disability": 1,
    "not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|not_provided|SYNE1-related_disorder": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_myogenic_arthrogryposis_multiplex_congenita": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 6,
    "not_provided|SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Inborn_genetic_diseases": 2,
    "SYNE1-related_disorder|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified|SYNE1-related_disorder": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided|SYNE1-related_disorder": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Skeletal_dysplasia": 1,
    "SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided": 3,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_provided|not_specified": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Rare_genetic_intellectual_disability": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder": 1,
    "not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Intellectual_disability|not_provided": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases|not_provided|SYNE1-related_disorder": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 2,
    "not_specified|not_provided|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 3,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Limb-girdle_muscular_dystrophy": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_specified": 2,
    "not_provided|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 4,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Charcot-Marie-Tooth_disease_type_1E|Hereditary_liability_to_pressure_palsies|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "not_specified|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided|SYNE1-related_disorder": 2,
    "not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified|not_provided": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Cardiomyopathy": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided|not_specified": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 3,
    "Distal_myopathy|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 2,
    "not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy|not_provided|not_specified|Cerebellar_ataxia": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|SYNE1-related_disorder": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 4,
    "SYNE1-related_disorder|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 4,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Abnormal_brain_morphology": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "not_provided|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|SYNE1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "not_specified|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder": 1,
    "SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified": 2,
    "not_provided|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 2,
    "Cerebellar_ataxia|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Hereditary_spherocytosis_type_3": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|SYNE1-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 2,
    "not_provided|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 6,
    "not_specified|SYNE1-related_disorder|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "Arthrogryposis_syndrome|Inborn_genetic_diseases|not_specified|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|SYNE1-related_disorder": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|SYNE1-related_disorder": 1,
    "Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided|Cerebellar_ataxia": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Inborn_genetic_diseases|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "Inborn_genetic_diseases|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided|not_specified": 2,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|SYNE1-related_disorder|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|not_specified": 1,
    "not_specified|Autosomal_recessive_ataxia|_Beauce_type|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder|not_specified|not_provided": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Intellectual_disability": 1,
    "SYNE1-related_disorder|Distal_myopathy|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "See_cases|not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|SYNE1-related_disorder": 1,
    "SYNE1-related_disorder|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided|Cerebellar_ataxia|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "SYNE1-related_disorder|Hereditary_ataxia|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified|not_provided": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|not_specified": 1,
    "not_specified|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|not_provided": 1,
    "SYNE1-related_disorder|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_specified": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|not_provided": 2,
    "Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Autosomal_recessive_ataxia|_Beauce_type|Spastic_ataxia|SYNE1-related_disorder": 1,
    "not_provided|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Autosomal_recessive_ataxia|_Beauce_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant": 1,
    "Autosomal_recessive_ataxia|_Beauce_type|Arthrogryposis_multiplex_congenita_3|_myogenic_type|Emery-Dreifuss_muscular_dystrophy_4|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Opioid_dependence|_susceptibility_to|_1|Tramadol_response": 1,
    "Tramadol_response|not_specified": 5,
    "not_specified|Tramadol_response": 3,
    "Coffin-Siris_syndrome_1|ARID1B-related_BAFopathy": 8,
    "ARID1B-related_disorder": 65,
    "not_provided|ARID1B-related_disorder": 23,
    "Coffin-Siris_syndrome_1|not_provided|Inborn_genetic_diseases": 6,
    "ARID1B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Coffin-Siris_syndrome_1": 6,
    "ARID1B-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|ARID1B-related_disorder|Inborn_genetic_diseases": 2,
    "Hereditary_ataxia|not_provided": 5,
    "not_specified|not_provided|ARID1B-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|ARID1B-related_disorder": 6,
    "not_provided|Coffin-Siris_syndrome_1|Inborn_genetic_diseases": 5,
    "Coffin-Siris_syndrome_1|not_provided": 38,
    "ARID1B-related_disorder|Inborn_genetic_diseases|not_provided": 8,
    "Coffin-Siris_syndrome_1|not_provided|ARID1B-related_disorder|Inborn_genetic_diseases": 2,
    "Intellectual_disability|Hirsutism": 2,
    "ARID1B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|not_specified|Coffin-Siris_syndrome_1": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|ARID1B-related_disorder": 1,
    "ARID1B-related_disorder|not_provided": 22,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|ARID1B-related_disorder": 1,
    "ARID1B-related_disorder|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ARID1B-related_disorder|not_provided": 4,
    "ARID1B-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "ARID1B-related_disorder|Coffin-Siris_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ARID1B-related_disorder|Inborn_genetic_diseases|Intellectual_disability|not_provided": 2,
    "not_specified|Coffin-Siris_syndrome_1|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|ARID1B-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|ARID1B-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|ARID1B-related_disorder": 8,
    "not_provided|Coffin-Siris_syndrome_1|Coffin-Siris_syndrome|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Coffin-Siris_syndrome_1|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Coffin-Siris_syndrome_1": 5,
    "not_provided|Coffin-Siris_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Coffin-Siris_syndrome_1|ARID1B-related_disorder|not_provided": 1,
    "ARID1B-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Coffin-Siris_syndrome_1": 7,
    "ARID1B-related_disorder|not_provided|Inborn_genetic_diseases": 5,
    "not_provided|ARID1B-related_disorder|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|ARID1B-related_disorder|not_specified|not_provided|Coffin-Siris_syndrome_1": 4,
    "Inborn_genetic_diseases|ARID1B-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|ARID1B-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|ARID1B-related_disorder|not_provided|not_specified": 1,
    "Coffin-Siris_syndrome_1|not_provided|ARID1B-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "ARID1B-related_disorder|not_provided|Inborn_genetic_diseases|Coffin-Siris_syndrome_1": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|ARID1B-related_disorder": 1,
    "Coffin-Siris_syndrome_1|not_provided|not_specified": 2,
    "not_provided|Coffin-Siris_syndrome_1|ARID1B-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|ARID1B-related_disorder|Coffin-Siris_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Coffin-Siris_syndrome_1": 4,
    "Intellectual_disability|ARID1B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ARID1B-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Coffin-Siris_syndrome_1|ARID1B-related_disorder|not_provided": 3,
    "Coffin-Siris_syndrome_1|Inborn_genetic_diseases|not_provided": 3,
    "Intellectual_disability|not_provided|Coffin-Siris_syndrome_1": 1,
    "Wiedemann-Steiner_syndrome": 253,
    "Inborn_genetic_diseases|ARID1B-related_disorder": 2,
    "Inborn_genetic_diseases|Coffin-Siris_syndrome_1": 2,
    "not_provided|ARID1B-related_disorder|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|ARID1B-related_BAFopathy|not_provided": 1,
    "Coffin_Siris/Intellectual_Disability": 2,
    "Coffin-Siris_syndrome_1|ARID1B-related_BAFopathy|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|Corpus_callosum|_agenesis_of": 1,
    "Inborn_genetic_diseases|Coffin-Siris_syndrome_1|not_provided": 11,
    "ARID1B-related_BAFopathy|not_provided": 1,
    "Coffin-Siris_syndrome_1|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|Inborn_genetic_diseases": 4,
    "not_provided|Coffin-Siris_syndrome_1|Corpus_callosum|_agenesis_of|Nail_dysplasia|Hypertrichosis|Neonatal_hypotonia|Global_developmental_delay|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|Inborn_genetic_diseases|ARID1B-related_BAFopathy": 1,
    "not_specified|Coffin-Siris_syndrome_1|ARID1B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|Nicolaides-Baraitser_syndrome": 1,
    "not_specified|Coffin-Siris_syndrome_1": 1,
    "ARID1B-related_BAFopathy": 17,
    "not_specified|Inborn_genetic_diseases|Coffin-Siris_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Coffin-Siris_syndrome_1|not_specified": 1,
    "not_specified|not_provided|Coffin-Siris_syndrome_1": 2,
    "ARID1B-related_disorder|not_provided|Coffin-Siris_syndrome_1|not_specified": 1,
    "Thick_lower_lip_vermilion|Thin_upper_lip_vermilion|Long_eyelashes|Intellectual_disability|_moderate|Absent_speech|Blepharophimosis": 2,
    "Inborn_genetic_diseases|not_specified|Coffin-Siris_syndrome_1|not_provided": 1,
    "ARID1B-related_BAFopathy|not_provided|Coffin-Siris_syndrome_1": 2,
    "Inborn_genetic_diseases|See_cases|ARID1B-related_disorder|not_provided|Coffin-Siris_syndrome_1": 1,
    "not_provided|ARID1B-related_BAFopathy": 2,
    "Coffin-Siris_syndrome_1|Autism_spectrum_disorder": 1,
    "Epilepsy|not_provided": 15,
    "ARID1B-related_BAFopathy|not_provided|Coffin-Siris_syndrome_1|Autism_spectrum_disorder": 1,
    "Inborn_genetic_diseases|Coffin_Siris/Intellectual_Disability|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|ARID1B-related_disorder": 1,
    "Blepharophimosis|Intellectual_disability|_moderate|Absent_speech|Thin_upper_lip_vermilion|Long_eyelashes|Thick_lower_lip_vermilion": 1,
    "ARID1B-related_BAFopathy|Coffin-Siris_syndrome_1": 5,
    "ARID1B-related_disorder|not_provided|not_specified|Coffin-Siris_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Coffin-Siris_syndrome_1|ARID1B-related_disorder|ARID1B-related_BAFopathy": 1,
    "not_provided|ARID1B-related_BAFopathy|Coffin-Siris_syndrome_1": 1,
    "ARID1B-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Coffin-Siris_syndrome_1": 1,
    "Coffin-Siris_syndrome_1|Medulloblastoma": 1,
    "Coffin-Siris_syndrome_1|Intellectual_disability": 1,
    "Global_developmental_delay|Delayed_speech_and_language_development|Bilateral_cryptorchidism|Hypertrichosis|Intellectual_disability|Abnormal_speech_pattern": 1,
    "ARID1B-related_disorder|not_specified|not_provided|Coffin-Siris_syndrome_1|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome|Coffin-Siris_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Coffin-Siris_syndrome_1|ARID1B-related_BAFopathy": 1,
    "ARID1B-related_BAFopathy|Inborn_genetic_diseases|Coffin-Siris_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Coffin-Siris_syndrome_1|ARID1B-related_disorder": 1,
    "not_specified|not_provided|ARID1B-related_disorder|Coffin-Siris_syndrome_1|Inborn_genetic_diseases": 1,
    "ARID1B-related_disorder|Coffin-Siris_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "Coffin_Siris/Intellectual_Disability|not_provided": 1,
    "Inborn_genetic_diseases|Decreased_body_weight|Constipation|Seizure|Short_stature|Failure_to_thrive|Microcephaly|Recurrent_respiratory_infections|See_cases|not_provided|Coffin-Siris_syndrome_1|ARID1B-related_disorder|ARID1B-related_BAFopathy": 1,
    "Coffin-Siris_syndrome_1|Coffin-Siris_syndrome": 1,
    "Thick_lower_lip_vermilion|Thin_upper_lip_vermilion|Long_eyelashes|Intellectual_disability|_moderate|Absent_speech|Blepharophimosis|Coffin-Siris_syndrome_1|not_provided": 1,
    "ARID1B-related_disorder|Inborn_genetic_diseases|Coffin-Siris_syndrome_1|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Coffin-Siris_syndrome_1": 2,
    "not_specified|Coffin-Siris_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Coffin-Siris_syndrome": 1,
    "Coffin-Siris_syndrome_1|not_provided|ARID1B-related_BAFopathy|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|not_specified": 1,
    "Coffin-Siris_syndrome_1|Marfanoid_habitus_and_intellectual_disability|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 1,
    "Coffin-Siris_syndrome|Coffin-Siris_syndrome_1": 1,
    "Coffin-Siris_syndrome_1|not_specified|not_provided": 2,
    "Metabolic_disease|Inborn_genetic_diseases": 1,
    "not_provided|ARID1B-related_disorder|Coffin-Siris_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly|Coffin-Siris_syndrome_1": 1,
    "Neurodevelopmental_delay|Coffin-Siris_syndrome": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 696,
    "not_provided|not_specified|Coffin-Siris_syndrome_1": 1,
    "Coffin-Siris_syndrome_1|Marfanoid_habitus_and_intellectual_disability": 1,
    "ARID1B-related_disorder|Coffin-Siris_syndrome_1|not_provided": 1,
    "Coffin-Siris_syndrome_1|ARID1B-related_BAFopathy|Inborn_genetic_diseases": 1,
    "dysmorphy|intellectual_deficiency": 1,
    "Rare_genetic_intellectual_disability|not_provided": 1,
    "not_provided|Coffin-Siris_syndrome|ARID1B-related_disorder|Inborn_genetic_diseases": 1,
    "Coffin-Siris_syndrome_1|ARID1B-related_disorder": 1,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 206,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_provided|SERAC1-related_disorder": 1,
    "not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 20,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 9,
    "not_specified|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 7,
    "SERAC1-related_disorder|not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 1,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|Inborn_genetic_diseases|SERAC1-related_disorder|not_provided": 1,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_provided": 15,
    "SERAC1-related_disorder|not_provided": 1,
    "not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|Inborn_genetic_diseases": 1,
    "SERAC1-related_neurological_disorder": 1,
    "SERAC1-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 2,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_specified": 5,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|SERAC1-related_disorder": 3,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|SERAC1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 6,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_provided": 1,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|SERAC1-related_disorder|not_provided|not_specified": 1,
    "not_specified|SERAC1-related_disorder|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 1,
    "not_specified|not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 4,
    "not_provided|not_specified|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 2,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_specified|not_provided": 2,
    "not_specified|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_provided": 1,
    "3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|Inborn_genetic_diseases": 6,
    "not_specified|Inborn_genetic_diseases|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 1,
    "not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|3-methylglutaconic_aciduria_with_deafness|_encephalopathy|_and_Leigh-like_syndrome": 1,
    "Mitochondrial_oxidative_phosphorylation_disorder": 1,
    "Leigh_syndrome|not_specified": 62,
    "Trichothiodystrophy_3|_photosensitive": 5,
    "Trichothiodystrophy_3|_photosensitive|not_provided": 1,
    "not_provided|Trichothiodystrophy_3|_photosensitive": 1,
    "Inborn_genetic_diseases|not_provided|Trichothiodystrophy_3|_photosensitive": 1,
    "GTF2H5-related_disorder": 1,
    "EZR-related_disorder|not_provided": 1,
    "EZR-related_disorder": 11,
    "not_provided|not_specified|EZR-related_disorder": 1,
    "Primary_ciliary_dyskinesia_32": 191,
    "RSPH3-related_disorder": 3,
    "Primary_ciliary_dyskinesia_32|not_provided": 7,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_32": 24,
    "not_provided|Primary_ciliary_dyskinesia_32": 13,
    "Primary_ciliary_dyskinesia_32|Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 1,
    "RSPH3-related_disorder|not_provided|Primary_ciliary_dyskinesia_32": 1,
    "RSPH3-related_disorder|Primary_ciliary_dyskinesia_32": 4,
    "Primary_ciliary_dyskinesia_32|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_32|not_provided": 1,
    "Primary_ciliary_dyskinesia_32|Inborn_genetic_diseases|RSPH3-related_disorder": 1,
    "Primary_ciliary_dyskinesia_32|RSPH3-related_disorder": 1,
    "Primary_ciliary_dyskinesia_32|Inborn_genetic_diseases|not_provided": 1,
    "Primary_ciliary_dyskinesia|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_32": 1,
    "Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia_32": 1,
    "not_specified|Microvascular_complications_of_diabetes|_susceptibility_to|_6": 1,
    "SOD2_POLYMORPHISM|Microvascular_complications_of_diabetes|_susceptibility_to|_6": 1,
    "Acetyl-CoA_acetyltransferase-2_deficiency": 1,
    "ZTTK_syndrome": 121,
    "Intellectual_developmental_disorder_with_polymicrogyria_and_seizures": 4,
    "Spermatogenic_failure_57": 4,
    "Spermatogenic_failure_57|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 2,
    "Oligospermia|Non-obstructive_azoospermia": 1,
    "not_specified|Non-obstructive_azoospermia": 1,
    "Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Spermatogenic_failure_57": 1,
    "LIPOPROTEIN(a)_POLYMORPHISM": 2,
    "Myofibrillar_myopathy_6|not_provided|LPA-related_disorder": 1,
    "not_provided|LIPOPROTEIN(a)_POLYMORPHISM": 1,
    "LPA-related_disorder": 2,
    "LIPOPROTEIN(a)_QUANTITATIVE_TRAIT_LOCUS": 1,
    "Lipoprotein(a)_deficiency|_congenital|not_specified|LPA-related_disorder": 1,
    "Lipoprotein(a)_deficiency|_congenital": 1,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|Inborn_genetic_diseases|not_provided": 4,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I": 54,
    "not_provided|Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I": 7,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|not_provided|Otitis_media|_susceptibility_to|Deep_venous_thrombosis": 1,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|not_provided": 18,
    "not_provided|not_specified|Inborn_genetic_diseases|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4": 1,
    "Plasminogen_deficiency|_type_I|not_provided|Angioedema|_hereditary|_4": 5,
    "Inborn_genetic_diseases|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4": 1,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|not_provided": 5,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|Hereditary_angioedema_type_1": 1,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|PLG-related_disorder|not_provided": 1,
    "not_provided|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4": 12,
    "not_specified|Inborn_genetic_diseases|PLG-related_disorder|not_provided": 1,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|Inborn_genetic_diseases": 2,
    "Plasminogen_deficiency|_type_I": 11,
    "not_provided|Plasminogen_deficiency|_type_I": 1,
    "Inborn_genetic_diseases|Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|not_provided": 2,
    "not_provided|Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4": 3,
    "Angioedema|_hereditary|_4|not_provided": 1,
    "not_specified|Angioedema|_hereditary|_4|not_provided|Plasminogen_deficiency|_type_I": 1,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|not_specified|not_provided": 2,
    "not_provided|Otitis_media|_susceptibility_to|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|PLG-related_disorder": 1,
    "not_specified|Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I": 1,
    "not_provided|PLG-related_disorder": 4,
    "Angioedema|_hereditary|_4|not_specified|Plasminogen_deficiency|_type_I|not_provided": 2,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|PLG-related_disorder|not_provided|Hereditary_angioneurotic_edema": 1,
    "not_provided|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|Inborn_genetic_diseases": 1,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|Inborn_genetic_diseases": 3,
    "Dysplasminogenemia": 2,
    "PLG-related_disorder": 4,
    "PLG-related_disorder|not_provided|Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|not_specified": 1,
    "not_specified|Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|not_provided": 1,
    "not_provided|Otitis_media|_susceptibility_to": 1,
    "PLG-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Deep_venous_thrombosis|Abnormal_bleeding|Thrombocytopenia|Plasminogen_deficiency|_type_I|Thrombus|not_provided|PLG-related_disorder": 1,
    "Otitis_media|_susceptibility_to|not_provided": 4,
    "PLG-related_disorder|not_provided": 5,
    "Plasminogen_deficiency|_type_I|Angioedema|_hereditary|_4|Atypical_hemolytic-uremic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Plasminogen_deficiency|_type_I|not_provided|not_specified|Dysplasminogenemia": 1,
    "not_provided|PLG-related_disorder|not_specified|Deep_venous_thrombosis": 1,
    "not_specified|Plasminogen_deficiency|_type_I|not_provided|Otitis_media|_susceptibility_to|Deep_venous_thrombosis": 1,
    "Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I|not_specified|not_provided": 1,
    "Angioedema|_hereditary|_4|Hereditary_angioedema_with_normal_C1Inh": 1,
    "not_provided|Inborn_genetic_diseases|Angioedema|_hereditary|_4|Plasminogen_deficiency|_type_I": 1,
    "not_provided|PLG-related_disorder|Dysplasminogenemia": 1,
    "Juvenile-onset_Parkinson_disease": 4,
    "not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2": 28,
    "Autosomal_recessive_juvenile_Parkinson_disease_2": 71,
    "Juvenile-onset_Parkinson_disease|not_provided": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Lung_cancer|Ovarian_neoplasm": 2,
    "Juvenile-onset_Parkinson_disease|PRKN-related_disorder|not_provided": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Lung_cancer|Ovarian_cancer|not_provided": 2,
    "Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_cancer|Parkinson_disease_12|not_specified|not_provided": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided": 11,
    "Young-onset_Parkinson_disease|Ovarian_cancer|Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided|PRKN-related_disorder": 1,
    "Young-onset_Parkinson_disease|not_provided": 1,
    "Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_cancer": 3,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided|Ovarian_cancer|Lung_cancer": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|PRKN-related_disorder|not_provided": 2,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Lung_cancer|Ovarian_neoplasm|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_neoplasm|Lung_cancer|not_specified": 1,
    "not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_neoplasm|Lung_cancer": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided|not_specified": 2,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_cancer|Lung_cancer|not_provided": 2,
    "PRKN-related_disorder|Autosomal_recessive_juvenile_Parkinson_disease_2|not_specified|not_provided": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Lung_cancer|Ovarian_neoplasm|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "not_provided|Autism_spectrum_disorder|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "Lung_cancer|Ovarian_neoplasm|Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided": 1,
    "Parkinson_disease_12|Lung_cancer|Ovarian_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2|PRKN-related_disorder|Young-onset_Parkinson_disease|Ovarian_neoplasm|Lung_carcinoma|Leprosy|_susceptibility_to|_2|not_provided|See_cases": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_neoplasm|Lung_cancer|not_provided": 2,
    "Ovarian_cancer|not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2|Lung_cancer": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_cancer|Lung_cancer|not_specified|not_provided": 1,
    "Young-onset_Parkinson_disease|not_provided|Ovarian_neoplasm|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "not_provided|Lung_cancer|Ovarian_neoplasm|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "Ovarian_cancer|not_provided|Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "PRKN-related_disorder": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Lung_adenocarcinoma": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided|Ovarian_neoplasm|Lung_cancer|not_specified": 1,
    "Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_neoplasm|not_provided": 5,
    "not_specified|not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "Ovarian_neoplasm|Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided": 1,
    "not_provided|Ovarian_cancer|Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2|Lung_cancer|Ovarian_neoplasm": 1,
    "not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2|not_specified": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided|Young-onset_Parkinson_disease": 1,
    "Ovarian_cancer|Lung_cancer|Autosomal_recessive_juvenile_Parkinson_disease_2": 1,
    "not_specified|Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided": 1,
    "PRKN-related_disorder|not_provided|Autosomal_recessive_juvenile_Parkinson_disease_2|Ovarian_cancer|Lung_cancer": 1,
    "PRKN-related_disorder|not_provided": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_specified|not_provided": 1,
    "Autosomal_recessive_juvenile_Parkinson_disease_2|not_provided|Autosomal_dominant_Parkinson_disease_1": 1,
    "not_provided|Young-onset_Parkinson_disease": 1,
    "Infantile-onset_generalized_dyskinesia_with_orofacial_involvement": 10,
    "PDE10A-related_disorder|not_provided": 10,
    "PDE10A-related_disorder": 4,
    "not_provided|PDE10A-related_disorder": 2,
    "Infantile-onset_generalized_dyskinesia_with_orofacial_involvement|Striatal_degeneration|_autosomal_dominant_2|not_provided": 2,
    "Infantile-onset_generalized_dyskinesia_with_orofacial_involvement|Striatal_degeneration|_autosomal_dominant_2": 2,
    "not_provided|Striatal_degeneration|_autosomal_dominant_2": 2,
    "not_provided|Infantile-onset_generalized_dyskinesia_with_orofacial_involvement|Striatal_degeneration|_autosomal_dominant_2": 2,
    "Global_developmental_delay|Generalized_hypotonia|Infantile-onset_generalized_dyskinesia_with_orofacial_involvement": 1,
    "Striatal_degeneration|_autosomal_dominant_2": 1,
    "not_specified|Sacral_agenesis-abnormal_ossification_of_the_vertebral_bodies-persistent_notochordal_canal_syndrome|Neural_tube_defects|_susceptibility_to": 2,
    "TBXT-related_disorder": 6,
    "TBXT-related_disorder|not_provided": 1,
    "not_provided|Sacral_agenesis-abnormal_ossification_of_the_vertebral_bodies-persistent_notochordal_canal_syndrome|Neural_tube_defects|_susceptibility_to": 1,
    "not_provided|Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome": 4,
    "Sacral_agenesis-abnormal_ossification_of_the_vertebral_bodies-persistent_notochordal_canal_syndrome": 3,
    "not_provided|TBXT-related_disorder": 1,
    "MPC1-related_disorder|not_provided": 1,
    "not_specified|Fraser_syndrome_3": 1,
    "Mitochondrial_pyruvate_carrier_deficiency": 8,
    "MPC1-related_disorder": 1,
    "not_provided|RNASET2-related_disorder": 3,
    "Cystic_leukoencephalopathy_without_megalencephaly": 39,
    "not_provided|Cystic_leukoencephalopathy_without_megalencephaly": 11,
    "Cystic_leukoencephalopathy_without_megalencephaly|not_specified": 2,
    "RNASET2-related_disorder|Cystic_leukoencephalopathy_without_megalencephaly|not_provided": 1,
    "Cystic_leukoencephalopathy_without_megalencephaly|not_provided": 4,
    "RNASET2-related_disorder|not_provided|Cystic_leukoencephalopathy_without_megalencephaly": 1,
    "Cystic_leukoencephalopathy_without_megalencephaly|Inborn_genetic_diseases": 1,
    "not_provided|Cystic_leukoencephalopathy_without_megalencephaly|RNASET2-related_disorder": 2,
    "Inborn_genetic_diseases|Cystic_leukoencephalopathy_without_megalencephaly|not_provided": 1,
    "SMOC2-related_disorder|not_provided": 2,
    "DENTIN_DYSPLASIA|_TYPE_I|_WITH_EXTREME_MICRODONTIA_AND_MISSHAPEN_TEETH|not_provided": 1,
    "not_specified|Dentin_dysplasia_type_I": 1,
    "SMOC2-related_disorder": 2,
    "not_provided|SMOC2-related_disorder": 1,
    "DENTIN_DYSPLASIA|_TYPE_I|_WITH_EXTREME_MICRODONTIA_AND_MISSHAPEN_TEETH": 1,
    "Dentin_dysplasia_type_I": 1,
    "Dentin_dysplasia_type_I|not_specified": 1,
    "THBS2-related_disorder": 23,
    "not_provided|THBS2-related_disorder": 2,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic-like|_3": 1,
    "Lumbar_disk_herniation|_susceptibility_to|THBS2-related_disorder": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic-like|_3": 1,
    "THBS2-related_disorder|not_provided": 1,
    "ERMARD-related_disorder|not_provided": 5,
    "ERMARD-related_disorder|not_provided|not_specified": 4,
    "not_provided|not_specified|ERMARD-related_disorder": 2,
    "Periventricular_nodular_heterotopia_6": 18,
    "not_provided|ERMARD-related_disorder": 5,
    "not_provided|Periventricular_nodular_heterotopia_6": 1,
    "Periventricular_nodular_heterotopia_6|not_provided|not_specified": 3,
    "ERMARD-related_disorder": 6,
    "Periventricular_nodular_heterotopia_6|not_provided": 1,
    "ERMARD-related_disorder|not_specified|not_provided": 2,
    "not_specified|ERMARD-related_disorder|not_provided": 1,
    "ERMARD-related_disorder|not_specified": 2,
    "not_provided|Periventricular_nodular_heterotopia_6|not_specified": 1,
    "not_specified|not_provided|ERMARD-related_disorder": 3,
    "Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures": 53,
    "DLL1-related_disorder": 13,
    "DLL1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Alobar_holoprosencephaly": 1,
    "not_provided|DLL1-related_disorder": 12,
    "Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|not_provided": 10,
    "not_provided|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|Inborn_genetic_diseases": 3,
    "not_provided|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures": 6,
    "Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|DLL1-related_disorder|Inborn_genetic_diseases": 3,
    "DLL1-related_disorder|not_provided": 5,
    "DLL1-related_disorder|not_provided|Holoprosencephaly_sequence": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures": 1,
    "not_provided|Inborn_genetic_diseases|DLL1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|not_provided": 1,
    "DLL1-related_disorder|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|not_provided": 1,
    "not_provided|See_cases|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures": 1,
    "not_provided|Neurodevelopmental_disorder_with_nonspecific_brain_abnormalities_and_with_or_without_seizures|not_specified": 1,
    "DLL1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_hypotonia|_and_absent_language": 2,
    "Spinocerebellar_ataxia_type_17": 4,
    "not_provided|Spinocerebellar_ataxia_type_17|Parkinson_disease|_late-onset": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_17": 1,
    "Parkinson_disease|_late-onset|Spinocerebellar_ataxia_type_17|not_specified|not_provided": 2,
    "Spinocerebellar_ataxia_type_17|Parkinson_disease|_late-onset|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_17": 1,
    "TBP-related_disorder": 1,
    "not_provided|FAM20C-related_disorder": 5,
    "FAM20C-related_disorder": 6,
    "not_provided|Inborn_genetic_diseases|FAM20C-related_disorder|not_specified": 1,
    "Lethal_osteosclerotic_bone_dysplasia": 19,
    "FAM20C-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|FAM20C-related_disorder|not_provided": 1,
    "not_provided|Lethal_osteosclerotic_bone_dysplasia|Inborn_genetic_diseases": 1,
    "FAM20C-related_disorder|not_provided|not_specified": 1,
    "not_provided|Lethal_osteosclerotic_bone_dysplasia": 9,
    "Inborn_genetic_diseases|Lethal_osteosclerotic_bone_dysplasia|not_provided": 2,
    "FAM20C-related_disorder|not_specified|not_provided": 1,
    "FAM20C-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|FAM20C-related_disorder": 1,
    "Lethal_osteosclerotic_bone_dysplasia|not_provided": 9,
    "not_provided|Lethal_osteosclerotic_bone_dysplasia|not_specified": 1,
    "ketotic_hypoglycaemia": 1,
    "FAM20C-related_disorder|not_specified|Lethal_osteosclerotic_bone_dysplasia|not_provided": 1,
    "Abnormal_facial_shape|Neonatal_death|Cortical_dysplasia|Severe_brain_malformation": 1,
    "not_specified|Lethal_osteosclerotic_bone_dysplasia|not_provided": 1,
    "Lethal_osteosclerotic_bone_dysplasia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Lethal_osteosclerotic_bone_dysplasia": 1,
    "Lethal_osteosclerotic_bone_dysplasia|not_specified|not_provided": 2,
    "not_provided|not_specified|Lethal_osteosclerotic_bone_dysplasia": 1,
    "Lethal_osteosclerotic_bone_dysplasia|not_provided|FAM20C-related_disorder": 1,
    "Splenomegaly|Delayed_gross_motor_development|Hepatic_fibrosis": 1,
    "Marbach-Schaaf_neurodevelopmental_syndrome": 11,
    "not_specified|PRKAR1B-related_disorder": 4,
    "not_provided|PRKAR1B-related_disorder": 7,
    "Marbach-Schaaf_neurodevelopmental_syndrome|PRKAR1B-related_neurodevelopmental_disorder|not_provided": 1,
    "PRKAR1B-related_disorder": 5,
    "PRKAR1B-related_disorder|not_provided": 5,
    "not_provided|Marbach-Schaaf_neurodevelopmental_syndrome": 1,
    "Marbach-Schaaf_neurodevelopmental_syndrome|not_specified": 1,
    "PRKAR1B-related_disorder|not_specified": 1,
    "DNAAF5-related_disorder|Primary_ciliary_dyskinesia": 10,
    "Primary_ciliary_dyskinesia_18": 6,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_18": 14,
    "not_provided|DNAAF5-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Congenital_heart_disease|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_18": 1,
    "not_provided|DNAAF5-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_18": 1,
    "DNAAF5-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_18|Primary_ciliary_dyskinesia": 10,
    "DNAAF5-related_disorder|Primary_ciliary_dyskinesia_18|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|DNAAF5-related_disorder|Primary_ciliary_dyskinesia_18": 1,
    "not_provided|Primary_ciliary_dyskinesia_18|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia|DNAAF5-related_disorder": 8,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_18": 3,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_18": 1,
    "DNAAF5-related_disorder": 2,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_18": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_18": 1,
    "Primary_ciliary_dyskinesia_18|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_18": 1,
    "Primary_ciliary_dyskinesia_18|DNAAF5-related_disorder|Primary_ciliary_dyskinesia": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_18": 1,
    "not_specified|Primary_ciliary_dyskinesia_18|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_18": 1,
    "not_provided|Primary_ciliary_dyskinesia_18": 1,
    "not_provided|DNAAF5-related_disorder": 1,
    "DNAAF5-related_disorder|Primary_ciliary_dyskinesia_18": 1,
    "Emery-Dreifuss_muscular_dystrophy": 770,
    "Emery-Dreifuss_muscular_dystrophy|not_specified": 66,
    "Emery-Dreifuss_muscular_dystrophy|not_provided": 28,
    "SUN1-related_disorder|Emery-Dreifuss_muscular_dystrophy": 19,
    "SUN1-related_disorder|not_provided|Emery-Dreifuss_muscular_dystrophy": 4,
    "not_specified|Emery-Dreifuss_muscular_dystrophy": 82,
    "not_provided|Emery-Dreifuss_muscular_dystrophy": 12,
    "SUN1-related_disorder|Emery-Dreifuss_muscular_dystrophy|not_provided": 3,
    "Emery-Dreifuss_muscular_dystrophy|SUN1-related_disorder": 3,
    "not_provided|Emery-Dreifuss_muscular_dystrophy|SUN1-related_disorder": 3,
    "not_provided|SUN1-related_disorder": 1,
    "Emery-Dreifuss_muscular_dystrophy|not_provided|SUN1-related_disorder": 1,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy": 2,
    "not_specified|Emery-Dreifuss_muscular_dystrophy|not_provided": 3,
    "not_specified|SUN1-related_disorder|Emery-Dreifuss_muscular_dystrophy": 1,
    "SUN1-related_disorder|not_specified|Emery-Dreifuss_muscular_dystrophy": 1,
    "Congenital_disorder_of_glycosylation|_type_IIy|GET4_deficiency|not_provided": 1,
    "Congenital_disorder_of_glycosylation|_type_IIy|GET4-related_disorder|GET4_deficiency": 1,
    "INTS1-related_disorder": 23,
    "Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies": 44,
    "not_provided|INTS1-related_disorder|Inborn_genetic_diseases": 1,
    "INTS1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|INTS1-related_disorder|Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies": 1,
    "Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies|not_specified": 1,
    "not_provided|INTS1-related_disorder": 10,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies": 2,
    "INTS1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies": 6,
    "Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies|Inborn_genetic_diseases": 5,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies": 2,
    "Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies|Neurodevelopmental_delay": 1,
    "Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies|not_provided": 2,
    "Neurodevelopmental_disorder_with_cataracts|_poor_growth|_and_dysmorphic_facies|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|INTS1-related_disorder": 1,
    "Developmental_and_Epileptic_Encephalopathy_with_Joint_Laxity|DURSUN-OZGUL_NEURODEVELOPMENTAL_SYNDROME": 1,
    "not_provided|not_specified|ELFN1-related_disorder": 1,
    "DURSUN-OZGUL_NEURODEVELOPMENTAL_SYNDROME": 4,
    "Mosaic_variegated_aneuploidy_syndrome_7_with_inflammation_and_tumor_predisposition": 3,
    "LYMPHOMA|_DIFFUSE_LARGE_B-CELL|_SOMATIC": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1": 433,
    "Prostate_cancer|_somatic|Prostate_cancer|not_provided": 1,
    "MRM2-related_disorder": 2,
    "Mitochondrial_DNA_depletion_syndrome_17": 2,
    "MRM2-related_disorder|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_17|not_provided": 1,
    "not_provided|MRM2-related_disorder": 2,
    "not_provided|LFNG-related_disorder": 1,
    "Spondylocostal_dysostosis_3|_autosomal_recessive": 180,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|Inborn_genetic_diseases": 5,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|LFNG-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Spondylocostal_dysostosis_3|_autosomal_recessive": 9,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|not_provided": 5,
    "not_provided|Spondylocostal_dysostosis_3|_autosomal_recessive": 3,
    "LFNG-related_disorder|Spondylocostal_dysostosis_3|_autosomal_recessive": 3,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|LFNG-related_disorder": 4,
    "not_provided|Spondylocostal_dysostosis_3|_autosomal_recessive|not_specified": 2,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 2,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|Spondylocostal_dysostosis_3|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|not_specified": 1,
    "LFNG-related_disorder|not_provided": 1,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|not_specified|not_provided": 1,
    "Spondylocostal_dysostosis_3|_autosomal_recessive|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Spondylocostal_dysostosis_3|_autosomal_recessive|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 3,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 804,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 63,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 57,
    "BRAT1-related_disorder|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 5,
    "Inborn_genetic_diseases|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 30,
    "not_specified|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 3,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|Inborn_genetic_diseases": 5,
    "not_specified|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 2,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|Inborn_genetic_diseases": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases": 28,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Intellectual_disability": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|Intellectual_disability|BRAT1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 5,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 6,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases|not_provided|BRAT1-related_disorder": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder": 6,
    "not_specified|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 4,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|BRAT1-related_disorder": 2,
    "BRAT1-related_disorder|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 3,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures": 18,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|BRAT1-related_disorder|Inborn_genetic_diseases": 4,
    "BRAT1-related_disorder|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Inborn_genetic_diseases|BRAT1-associated_neurodegenerative_disorder|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases|not_specified|Intellectual_disability|not_provided": 1,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures": 6,
    "Inborn_genetic_diseases|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 5,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases|not_provided": 11,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_specified": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|not_specified": 2,
    "BRAT1-related_neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "not_provided|not_specified|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 2,
    "not_provided|BRAT1-related_disorder|not_specified|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases": 9,
    "BRAT1-related_disorder|not_specified|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "BRAT1-related_disorder|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 3,
    "BRAT1-related_disorder": 7,
    "not_specified|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|not_provided": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases|not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Inborn_genetic_diseases|not_provided": 2,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|not_specified|BRAT1-related_disorder": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures": 6,
    "BRAT1-related_disorder|Inborn_genetic_diseases|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 1,
    "BRAT1-related_disorder|Intellectual_disability|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 7,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder|not_provided": 2,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder|not_specified": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|not_specified": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability|Inborn_genetic_diseases|BRAT1-related_disorder|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures": 2,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_specified|not_provided": 1,
    "BRAT1-related_disorder|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|BRAT1-related_disorder": 1,
    "BRAT1-related_disorder|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|BRAT1-related_disorder|not_provided": 1,
    "Neonatal-onset_encephalopathy_with_rigidity_and_seizures|not_provided|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|BRAT1-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures|Inborn_genetic_diseases|BRAT1-related_disorder|not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "not_provided|Neonatal-onset_encephalopathy_with_rigidity_and_seizures|Neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|Neonatal-onset_encephalopathy_with_rigidity_and_seizures": 1,
    "IQCE-related_disorder": 14,
    "Polydactyly|_postaxial|_type_a7": 12,
    "not_provided|Polydactyly|_postaxial|_type_a7": 1,
    "Polydactyly|_postaxial|_type_a7|IQCE-related_disorder": 10,
    "not_specified|IQCE-related_disorder": 1,
    "Polydactyly|_postaxial|_type_a7|not_provided": 1,
    "IQCE-related_disorder|not_provided": 4,
    "IQCE-related_disorder|Polydactyly|_postaxial|_type_a7": 3,
    "IQCE-related_disorder|Retinal_degeneration|Polydactyly|_postaxial|_type_A1|Syndactyly|Brachydactyly|not_provided|Polydactyly|_postaxial|_type_a7": 1,
    "not_provided|IQCE-related_disorder": 4,
    "IQCE-related_disorder|Polydactyly|_postaxial|_type_a7|Polydactyly|_postaxial|_type_A1": 1,
    "not_specified|not_provided|IQCE-related_disorder": 1,
    "BENTA_disease": 9,
    "BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_specified|not_provided": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 424,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Inborn_genetic_diseases": 13,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 429,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|CARD11-related_disorder|not_provided": 1,
    "not_provided|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 16,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis": 8,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_provided": 27,
    "not_provided|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 6,
    "BENTA_disease|not_provided|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "Inborn_genetic_diseases|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 6,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|Immunodeficiency_11b_with_atopic_dermatitis|BENTA_disease|not_specified|not_provided": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis": 9,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_provided": 9,
    "not_specified|BENTA_disease|not_provided|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_provided|not_specified": 2,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified|CARD11-related_disorder": 2,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified|not_provided": 3,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|Inborn_genetic_diseases": 7,
    "not_provided|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 6,
    "CARD11-related_disorder|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 8,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|CARD11-related_disorder|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_provided": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 3,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|CARD11-related_disorder": 5,
    "not_provided|CARD11-related_disorder|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 2,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|CARD11-related_disorder|not_specified|not_provided": 2,
    "not_specified|CARD11-related_disorder|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_provided": 1,
    "CARD11-related_disorder|not_provided|not_specified|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_provided": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_specified|not_provided": 5,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|CARD11-related_disorder|Immunodeficiency_11b_with_atopic_dermatitis|not_provided": 1,
    "not_specified|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_provided": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|Immunodeficiency_11b_with_atopic_dermatitis|not_provided": 2,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 5,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis|not_specified": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|Immunodeficiency_11b_with_atopic_dermatitis": 6,
    "CARD11-related_disorder|Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified": 4,
    "not_specified|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 9,
    "Immunodeficiency_11b_with_atopic_dermatitis|not_specified|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Hemophagocytosis": 1,
    "not_specified|not_provided|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 2,
    "not_provided|Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_specified": 7,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|CARD11-related_disorder": 3,
    "not_provided|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_specified": 1,
    "not_provided|BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "CARD11-related_disorder": 3,
    "not_specified|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|Immunodeficiency_11b_with_atopic_dermatitis|BENTA_disease|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Inborn_genetic_diseases|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "Inborn_genetic_diseases|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_provided": 1,
    "CARD11-related_disorder|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 4,
    "Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|CARD11-related_disorder|not_specified": 1,
    "BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|CARD11-related_disorder": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified|not_provided": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|not_specified|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 1,
    "CARD11-related_disorder|not_specified|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_specified|Immunodeficiency_11b_with_atopic_dermatitis": 1,
    "not_provided|CARD11-related_disorder|not_specified|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|CARD11-related_disorder|not_specified": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|not_specified": 1,
    "not_provided|not_specified|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|Asthma|Splenomegaly|Osteopenia|not_provided": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|Inborn_genetic_diseases": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease|not_provided": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency|BENTA_disease": 2,
    "not_specified|not_provided|BENTA_disease|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "BENTA_disease|Immunodeficiency_11b_with_atopic_dermatitis|Severe_combined_immunodeficiency_due_to_CARD11_deficiency": 1,
    "Immunodeficiency_11b_with_atopic_dermatitis|not_provided": 1,
    "Hereditary_spastic_paraplegia_48": 569,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|not_provided": 4,
    "not_provided|Hereditary_spastic_paraplegia_48|not_specified": 2,
    "AP5Z1-related_disorder": 5,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_48": 27,
    "Hereditary_spastic_paraplegia_48|Macular_dystrophy_with_or_without_extraocular_features|not_provided": 2,
    "Hereditary_spastic_paraplegia_48|Retinal_dystrophy": 5,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia": 15,
    "Hereditary_spastic_paraplegia_48|not_provided": 43,
    "not_provided|Hereditary_spastic_paraplegia_48": 32,
    "Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases": 36,
    "Macular_dystrophy_with_or_without_extraocular_features": 15,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_48|not_provided": 2,
    "Hereditary_spastic_paraplegia_48|not_specified": 4,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48": 7,
    "not_provided|Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_48|not_provided|Hereditary_spastic_paraplegia": 4,
    "Hereditary_spastic_paraplegia_48|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_48|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia": 5,
    "Retinal_dystrophy|not_provided|Hereditary_spastic_paraplegia_48": 1,
    "AP5Z1-related_disorder|Hereditary_spastic_paraplegia_48|not_provided": 1,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_48": 4,
    "Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder": 5,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48": 3,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48": 3,
    "Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder|not_provided|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_48|not_provided|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_48": 5,
    "Hereditary_spastic_paraplegia_48|not_provided|Hereditary_spastic_paraplegia|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|Retinal_dystrophy": 1,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|not_provided": 4,
    "Hereditary_spastic_paraplegia_48|High_myopia|not_provided|Inborn_genetic_diseases": 1,
    "AP5Z1-related_disorder|Hereditary_spastic_paraplegia_48": 1,
    "Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_48|not_provided|not_specified|Hereditary_spastic_paraplegia": 2,
    "Retinal_dystrophy|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_48": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|AP5Z1-related_disorder|Hereditary_spastic_paraplegia_48": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_48": 1,
    "not_provided|Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia_48|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_48|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_48|Macular_dystrophy_with_or_without_extraocular_features": 1,
    "Hereditary_spastic_paraplegia_48|not_provided|Macular_dystrophy_with_or_without_extraocular_features|Retinal_dystrophy": 1,
    "Hereditary_spastic_paraplegia_48|Macular_dystrophy_with_or_without_extraocular_features": 2,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Optic_atrophy": 1,
    "AP5Z1-related_disorder|Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_48": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_48|Macular_dystrophy_with_or_without_extraocular_features": 1,
    "not_provided|Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia": 2,
    "not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_48": 1,
    "not_specified|Hereditary_spastic_paraplegia_48|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_48": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_48": 2,
    "Hereditary_spastic_paraplegia_48|Retinal_dystrophy|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spastic_paraplegia_48|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_48|not_provided|Hereditary_spastic_paraplegia": 1,
    "AP5Z1-related_disorder|not_provided|Hereditary_spastic_paraplegia_48|not_specified": 1,
    "Retinal_dystrophy|Hereditary_spastic_paraplegia_48": 1,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_48": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_48|not_provided|Retinal_dystrophy|Hereditary_spastic_paraplegia|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_48|not_specified": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_48": 2,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_48|Retinal_dystrophy|not_provided": 1,
    "AP5Z1-related_disorder|Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_specified": 1,
    "AP5Z1-related_disorder|Hereditary_spastic_paraplegia_48|not_specified": 1,
    "Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|not_specified|Inborn_genetic_diseases|not_provided|Retinal_dystrophy": 1,
    "Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Retinal_dystrophy|Hereditary_spastic_paraplegia_48": 1,
    "Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Hereditary_spastic_paraplegia_48|Optic_atrophy": 1,
    "not_specified|Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|not_provided|AP5Z1-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_48|AP5Z1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_48|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_48|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Spastic_Paraplegia|_Recessive": 10,
    "MMD2-related_condition": 1,
    "Intellectual_developmental_disorder_with_short_stature_and_variable_skeletal_anomalies": 5,
    "WIPI2-related_disorder": 8,
    "not_provided|WIPI2-related_disorder": 5,
    "WIPI2-related_disorder|not_provided": 2,
    "SLC29A4-related_disorder": 17,
    "SLC29A4-related_disorder|not_provided": 1,
    "not_specified|SLC29A4-related_disorder": 1,
    "not_provided|SLC29A4-related_disorder": 2,
    "TNRC18-related_disorder": 1,
    "Baraitser-Winter_syndrome_1": 296,
    "ACTB-related_disorder": 9,
    "Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|not_provided": 8,
    "ACTB-associated_syndromic_thrombocytopenia": 4,
    "Baraitser-Winter_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "ACTB-associated_syndromic_thrombocytopenia|Baraitser-Winter_syndrome_1|Thrombocytopenia": 1,
    "ACTB-related_disorder|Baraitser-Winter_syndrome_1|not_provided": 1,
    "not_provided|Baraitser-Winter_syndrome_1|Baraitser-Winter_syndrome": 1,
    "Developmental_malformations-deafness-dystonia_syndrome": 2,
    "ACTB-related_BAFopathy|Baraitser-Winter_syndrome_1|not_provided": 1,
    "Developmental_malformations-deafness-dystonia_syndrome|not_provided|Baraitser-Winter_syndrome_1": 2,
    "not_provided|Baraitser-Winter_syndrome_1|Intellectual_disability": 1,
    "not_specified|Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1": 2,
    "Baraitser-Winter_syndrome_1|Inborn_genetic_diseases": 3,
    "Baraitser-Winter_syndrome_1|ACTB-related_disorder|Developmental_malformations-deafness-dystonia_syndrome|not_provided": 1,
    "Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 9,
    "Baraitser-Winter_syndrome_1|not_provided": 17,
    "Developmental_malformations-deafness-dystonia_syndrome|not_specified|not_provided|Baraitser-Winter_syndrome_1": 1,
    "not_specified|ACTB-related_disorder|Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1": 1,
    "Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1|not_specified": 2,
    "not_provided|Baraitser-Winter_syndrome_1": 22,
    "Baraitser-Winter_syndrome_1|ACTB-related_disorder": 4,
    "ACTB_Haploinsufficiency_syndrome|not_provided": 1,
    "Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|not_specified": 1,
    "ACTB-related_disorder|not_provided|Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1": 1,
    "Baraitser-Winter_syndrome_1|Becker_nevus_syndrome|ACTB-associated_syndromic_thrombocytopenia|Congenital_smooth_muscle_hamartoma|_with_or_without_hemihypertrophy|Developmental_malformations-deafness-dystonia_syndrome": 1,
    "Baraitser-Winter_syndrome_1|Cleft_palate|not_provided": 1,
    "not_provided|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|not_specified|ACTB-related_disorder": 1,
    "ACTB-related_disorder|not_provided|Baraitser-Winter_syndrome_1": 2,
    "ACTB-related_disorder|Baraitser-Winter_syndrome_1": 7,
    "not_provided|Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1": 1,
    "ACTB-related_disorder|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|not_provided": 1,
    "ACTB-related_BAFopathy|not_provided|Baraitser-Winter_syndrome_1": 2,
    "ACTB-related_BAFopathy|Inborn_genetic_diseases|not_provided|Baraitser-Winter_syndrome_1": 1,
    "not_provided|Baraitser-Winter_syndrome_1|Inborn_genetic_diseases|See_cases": 1,
    "ACTB-related_disorder|not_provided|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 1,
    "Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1": 2,
    "not_provided|Baraitser-Winter_syndrome_1|Inborn_genetic_diseases": 1,
    "Aminoacylase_1_deficiency|Baraitser-Winter_syndrome_1|ACTB-related_BAFopathy": 1,
    "Inborn_genetic_diseases|not_provided|Baraitser-Winter_syndrome_1": 1,
    "ACTB-related_BAFopathy|Inborn_genetic_diseases|not_provided|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 1,
    "Inborn_genetic_diseases|Baraitser-Winter_syndrome_1": 1,
    "ACTB-associated_syndromic_thrombocytopenia|Baraitser-Winter_syndrome_1|not_provided": 1,
    "Baraitser-Winter_syndrome_1|not_provided|Developmental_malformations-deafness-dystonia_syndrome": 1,
    "Becker_nevus_syndrome": 1,
    "Becker_nevus_syndrome|Baraitser-Winter_syndrome_1|BECKER_NEVUS_SYNDROME|_SOMATIC|_MOSAIC|BECKER_NEVUS|_SOMATIC|_MOSAIC|CONGENITAL_SMOOTH_MUSCLE_HAMARTOMA|_SOMATIC|_MOSAIC": 1,
    "Congenital_smooth_muscle_hamartoma|BECKER_NEVUS|_ISOLATED|_SOMATIC|_MOSAIC|CONGENITAL_SMOOTH_MUSCLE_HAMARTOMA_WITH_HEMIHYPERTROPHY|_SOMATIC|_MOSAIC|Becker_nevus_syndrome": 1,
    "CONGENITAL_SMOOTH_MUSCLE_HAMARTOMA|_SOMATIC|_MOSAIC": 2,
    "CONGENITAL_SMOOTH_MUSCLE_HAMARTOMA|_SOMATIC|_MOSAIC|Congenital_smooth_muscle_hamartoma": 2,
    "ACTB-related_disorder|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 1,
    "Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|not_specified|not_provided|ACTB-related_disorder": 1,
    "not_specified|Developmental_malformations-deafness-dystonia_syndrome|not_provided|Baraitser-Winter_syndrome_1|ACTB-related_disorder": 1,
    "Congenital_smooth_muscle_hamartoma": 2,
    "Developmental_malformations-deafness-dystonia_syndrome|Baraitser-Winter_syndrome_1|not_provided": 1,
    "not_provided|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 3,
    "Baraitser-Winter_syndrome|Baraitser-Winter_syndrome_1": 2,
    "ACTB-related_disorder|not_provided": 1,
    "Baraitser-Winter_syndrome_1|not_provided|ACTB-related_disorder": 1,
    "Neurodevelopmental_delay|Baraitser-Winter_syndrome_1": 1,
    "ACTB-related_disorder|Baraitser-Winter_syndrome_1|not_specified|not_provided": 1,
    "Intellectual_disability|Baraitser-Winter_syndrome_1|not_provided": 1,
    "Abnormal_brain_morphology|Short_stature|Microcephaly": 1,
    "Intellectual_disability|Baraitser-Winter_syndrome_1": 1,
    "Baraitser-Winter_syndrome_1|See_cases": 1,
    "not_provided|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|ACTB-related_disorder|not_specified": 1,
    "not_specified|Baraitser-Winter_syndrome_1": 2,
    "Developmental_malformations-deafness-dystonia_syndrome|not_provided|ACTB-related_disorder|Baraitser-Winter_syndrome_1": 1,
    "ACTB-related_BAFopathy|Baraitser-Winter_syndrome_1": 2,
    "not_specified|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 2,
    "Baraitser-Winter_syndrome|Baraitser-Winter_syndrome_1|not_provided": 1,
    "not_provided|ACTB-related_disorder|Baraitser-Winter_syndrome_1": 1,
    "ACTB-related_disorder|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome|not_specified|not_provided": 1,
    "ACTB-related_BAFopathy": 1,
    "Baraitser-Winter_syndrome_1|Intellectual_disability": 1,
    "not_provided|not_specified|Baraitser-Winter_syndrome_1|Developmental_malformations-deafness-dystonia_syndrome": 1,
    "Cerebellar_ataxia-hypogonadism_syndrome": 24,
    "not_provided|RNF216-related_disorder": 1,
    "RNF216-related_disorder|not_provided": 7,
    "RNF216-related_disorder": 4,
    "Rosette-forming_glioneuronal_tumor": 2,
    "not_provided|Cerebellar_ataxia-hypogonadism_syndrome": 2,
    "Leukodystrophy|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Cerebellar_ataxia-hypogonadism_syndrome|not_provided|RNF216-related_disorder": 1,
    "Cerebellar_ataxia-hypogonadism_syndrome|not_provided": 1,
    "RNF216-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Lynch_syndrome_4": 3,
    "Lynch_syndrome_4|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_4|not_specified": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 3,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|PMS2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 71,
    "Mismatch_repair_cancer_syndrome_4": 9,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 60,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 47,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Endometrial_carcinoma|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_4": 3,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 5,
    "not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 74,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 3,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 77,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 55,
    "Lynch_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 3,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 95,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Lynch_syndrome_4|not_provided": 1,
    "PMS2-related_disorder|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 5,
    "not_provided|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 46,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 7,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 69,
    "not_specified|Lynch_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 79,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_4": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4": 6,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "not_specified|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified": 5,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 2,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Ovarian_cancer|not_specified|Hereditary_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 8,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_4|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Mismatch_repair_cancer_syndrome_1|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Inherited_MMR_deficiency_(Lynch_syndrome)|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 7,
    "not_specified|PMS2-related_disorder|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 10,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4": 9,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Breast_and/or_ovarian_cancer|not_provided|Mismatch_repair_cancer_syndrome_4": 1,
    "not_provided|Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 7,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4": 2,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|not_specified|Lynch_syndrome_4": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_4|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4": 5,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 17,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|not_provided": 4,
    "not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_4|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 7,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Lynch_syndrome_4|Endometrial_carcinoma|Hereditary_cancer|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_provided|not_specified|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder": 1,
    "Lynch_syndrome|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Cancer_or_benign_tumor|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 5,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_specified|not_provided|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|not_specified|Breast_and/or_ovarian_cancer|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|not_specified|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 1,
    "Lynch_syndrome_1|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Lynch_syndrome_4|PMS2-related_disorder|not_provided|not_specified": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Breast_neoplasm|not_specified|Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome_4|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_1|Lynch_syndrome_4|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_4": 2,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 2,
    "Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 2,
    "Lynch_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome|not_provided": 1,
    "not_specified|Lynch_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Ovarian_neoplasm|Lynch_syndrome_4|Endometrial_carcinoma": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_4|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Lynch_syndrome_1|Lynch_syndrome_4|Lynch_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|not_provided|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch-like_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome_4|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_4|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|PMS2-related_disorder": 1,
    "PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|not_provided|PMS2-related_disorder|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|not_specified|Lynch_syndrome": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 10,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Carcinoma_of_colon": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_specified|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4": 4,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|Lynch_syndrome|not_provided|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 4,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome_4|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|PMS2-related_disorder|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_4": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Lynch_syndrome_4": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 7,
    "Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Ovarian_neoplasm|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 2,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|not_provided|Lynch_syndrome_5": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 3,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 2,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 6,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_4|not_specified|not_provided": 1,
    "Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Malignant_tumor_of_breast": 2,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome_4|not_provided|Malignant_tumor_of_breast|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|not_specified|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Lynch_syndrome_4|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "PMS2-related_disorder": 2,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Lynch_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Endometrial_carcinoma|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4": 5,
    "not_provided|Lynch_syndrome|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|PMS2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Lynch_syndrome_4|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 2,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome": 3,
    "Lynch_syndrome|not_specified|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|PMS2-related_disorder|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Lynch_syndrome_4|not_provided|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Lynch_syndrome_4|Malignant_tumor_of_breast|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 2,
    "Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|PMS2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 2,
    "PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Malignant_tumor_of_breast|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Lynch_syndrome_4": 9,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 4,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome": 1,
    "Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome_4|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4": 2,
    "Lynch_syndrome_4|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 3,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_4": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|not_provided|Lynch_syndrome_4": 1,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|PMS2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Lynch_syndrome_4": 1,
    "Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Lynch_syndrome_4|not_specified|not_provided|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Ovarian_cancer|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_1|not_provided|Mismatch_repair_cancer_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_4|not_provided|PMS2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Colorectal_cancer|_non-polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Malignant_tumor_of_breast": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Inherited_MMR_deficiency_(Lynch_syndrome)|Lynch_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_4|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_1|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified|Lynch_syndrome": 1,
    "PMS2-related_disorder|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome_1": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Lynch_syndrome_4|Lynch_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_specified": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "PMS2-related_disorder|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|not_provided|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 2,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 2,
    "not_provided|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_carcinoma": 1,
    "Ovarian_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Lynch-like_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|not_provided|Lynch_syndrome_4": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "not_provided|Breast_neoplasm|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 2,
    "not_specified|not_provided|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4|PMS2-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4|not_specified|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Lynch_syndrome|Lynch_syndrome_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Burkitt_lymphoma|Lymphoma|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "not_specified|not_provided|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_4|not_specified|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 1,
    "not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Lynch_syndrome|Lynch_syndrome_4|not_specified|Mismatch_repair_cancer_syndrome_1|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Malignant_tumor_of_breast|not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Breast_carcinoma": 23,
    "Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|PMS2-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Inherited_MMR_deficiency_(Lynch_syndrome)": 1,
    "Lynch_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Lynch_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|not_provided|Lynch_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Malignant_tumor_of_breast": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Breast_and/or_ovarian_cancer": 1,
    "Polyp_of_colon|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Endometrial_carcinoma|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_4|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Lynch_syndrome_4|not_provided|Lynch_syndrome|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4": 1,
    "PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided|Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4": 1,
    "PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Mismatch_repair_cancer_syndrome_4|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Lynch_syndrome_4|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|Lynch_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Carcinoma_of_colon": 1,
    "not_provided|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 2,
    "Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|PMS2-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Malignant_tumor_of_breast|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_1|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lynch_syndrome_4|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Breast_and/or_ovarian_cancer|not_specified|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "not_specified|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 2,
    "not_provided|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Mismatch_repair_cancer_syndrome_1|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Lynch_syndrome": 1,
    "not_provided|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|not_provided|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|not_specified|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|not_provided": 1,
    "Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|not_provided|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_breast_ovarian_cancer_syndrome|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided|PMS2-related_disorder": 1,
    "Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome": 1,
    "Lynch_syndrome_4|PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Inherited_MMR_deficiency_(Lynch_syndrome)|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4|Polyp_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Lynch_syndrome_4|Lynch_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "not_specified|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_1|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_provided|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|not_specified": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 2,
    "Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified": 1,
    "PMS2-related_disorder|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Lynch_syndrome_4|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch-like_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Lynch_syndrome_4|not_specified|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_nonpolyposis_colon_cancer|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_1": 1,
    "Carcinoma_of_colon|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Lynch_syndrome": 2,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4": 1,
    "Lynch_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided": 1,
    "not_specified|Lynch_syndrome|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|not_specified|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|not_provided|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|Inherited_MMR_deficiency_(Lynch_syndrome)|PMS2-related_disorder|PMS2-related_cancer_disorders|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Dilated_cardiomyopathy_1G|Hypertrophic_cardiomyopathy_9|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1|Pituitary_carcinoma": 1,
    "Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|PMS2-related_disorder|not_specified|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_provided|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided": 1,
    "PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Carcinoma_of_colon|not_provided": 1,
    "Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_specified|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PMS2-related_disorder|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_specified|not_provided|Lynch_syndrome|Endometrial_carcinoma|Lynch_syndrome_1|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|PMS2-related_disorder|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "not_provided|PMS2-related_disorder|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Breast_and/or_ovarian_cancer|not_specified|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Endometrial_carcinoma|Lynch_syndrome_1|Mismatch_repair_cancer_syndrome_1": 1,
    "not_specified|Lynch_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|PMS2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|not_specified|Lynch_syndrome_4": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Lynch_syndrome|not_provided": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Lynch_syndrome|PMS2-related_disorder": 1,
    "Endometrial_carcinoma|Lynch_syndrome_4": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|not_provided|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PMS2-related_disorder|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome|Mismatch_repair_cancer_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Breast_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "not_specified|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Lynch_syndrome|Lynch_syndrome_4|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lynch_syndrome|Lynch_syndrome_4|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Mismatch_repair_cancer_syndrome_4|Lynch_syndrome_4|not_provided|Lynch_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Endometrial_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|Breast_and/or_ovarian_cancer|Lynch_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|Gastric_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4": 1,
    "PMS2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_4|not_provided|Lynch_syndrome": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4|Endometrial_carcinoma": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_nonpolyposis_colon_cancer|PMS2-related_disorder|Mismatch_repair_cancer_syndrome_4|Hereditary_cancer-predisposing_syndrome|not_provided|Lynch_syndrome|Lynch_syndrome_4|Mismatch_repair_cancer_syndrome_1|Lynch_syndrome_1": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_nonpolyposis_colorectal_neoplasms|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4": 1,
    "Lynch_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lynch_syndrome_4|not_provided|Lynch_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colorectal_neoplasms|Lynch_syndrome_4|PMS2-related_disorder|not_specified|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Lynch_syndrome|Mismatch_repair_cancer_syndrome_4|not_provided": 1,
    "Leukodystrophy|_hypomyelinating|_17|not_provided": 1,
    "not_provided|AIMP2-related_disorder": 3,
    "AIMP2-related_disorder|not_provided": 3,
    "Leukodystrophy|_hypomyelinating|_17|Inborn_genetic_diseases": 2,
    "Leukodystrophy|_hypomyelinating|_17": 4,
    "Leukodystrophy|_hypomyelinating|_17|Neurodevelopmental_abnormality": 1,
    "AIMP2-related_disorder": 3,
    "not_provided|Leukodystrophy|_hypomyelinating|_17": 1,
    "Leukoencephalopathy|_motor_delay|_spasticity|_and_dysarthria_syndrome|EIF2AK1-related_disorder": 1,
    "EIF2AK1-related_disorder": 1,
    "not_provided|Leukoencephalopathy|_motor_delay|_spasticity|_and_dysarthria_syndrome": 1,
    "EIF2AK1-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_48|not_provided": 5,
    "RAC1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_delay|Intellectual_disability|_autosomal_dominant_48|Global_developmental_delay|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_48": 3,
    "Intellectual_disability|_autosomal_dominant_48|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_48|See_cases": 1,
    "RAC1-related_disorder": 3,
    "not_provided|RAC1-related_disorder": 1,
    "KDELR2-related_disorder": 2,
    "Osteogenesis_imperfecta|_type_21": 6,
    "not_provided|Osteogenesis_imperfecta|_type_21": 1,
    "Glucocorticoid_therapy|_response_to": 1,
    "ICA1-related_disorder": 1,
    "NDUFA4-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_21": 3,
    "not_provided|NDUFA4-related_disorder": 1,
    "not_specified|NDUFA4-related_disorder": 1,
    "THSD7A-related_disorder": 7,
    "not_specified|THSD7A-related_disorder": 1,
    "Leukodystrophy|_hypomyelinating|_16": 9,
    "TMEM106B-related_disorder": 1,
    "not_provided|TMEM106B-related_disorder": 1,
    "Inborn_genetic_diseases|Leukodystrophy|_hypomyelinating|_16": 1,
    "Leukodystrophy|_hypomyelinating|_16|not_provided": 2,
    "not_provided|Leukodystrophy|_hypomyelinating|_16": 1,
    "Optic_atrophy_12": 6,
    "AGMO-related_disorder|not_specified": 1,
    "AGMO-related_disorder": 11,
    "AGMO-related_Neurodevelopmental_disorder": 2,
    "AGMO-related_disorder|not_provided": 1,
    "not_provided|AGMO-related_disorder": 2,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 163,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided": 9,
    "not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 8,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|not_provided": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 14,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 107,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 132,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_specified": 5,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided": 16,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified": 9,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 11,
    "not_specified|not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 21,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified|not_provided": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 13,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 2,
    "CRPPA-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_8|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 2,
    "not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided|not_specified": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_specified|not_provided": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 5,
    "not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided|CRPPA-related_disorder": 2,
    "CRPPA-related_disorder": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified": 1,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 661,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_specified": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified|not_provided": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified|not_provided": 1,
    "CRPPA-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided": 1,
    "ISPD-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 3,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified": 1,
    "CRPPA-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|CRPPA-related_disorder": 1,
    "not_specified|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7": 1,
    "ISPD-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_specified": 1,
    "CRPPA-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_specified": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|CRPPA-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified|not_provided": 1,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 2,
    "not_specified|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2U|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_7|not_specified|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|CRPPA-related_disorder|not_provided": 1,
    "Respiratory_infections|_recurrent|_and_failure_to_thrive_with_or_without_diarrhea": 7,
    "AGR2-related_disorder": 1,
    "Respiratory_infections|_recurrent|_and_failure_to_thrive_with_or_without_diarrhea|AGR2-related_disorder": 1,
    "Retinitis_pigmentosa_85": 3,
    "not_provided|AHR-related_disorder": 2,
    "AHR-related_disorder|not_provided": 10,
    "Foveal_hypoplasia_3": 2,
    "GH-secreting_pituitary_adenoma": 1,
    "not_provided|Retinitis_pigmentosa_85": 1,
    "Foveal_hypoplasia_3|Infantile_nystagmus_with_foveal_hypoplasia": 1,
    "SLC25A18-related_disorder": 1,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome": 49,
    "Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis": 37,
    "TWIST1-related_craniosynostosis": 67,
    "Saethre-Chotzen_syndrome": 19,
    "Robinow-Sorauf_syndrome": 2,
    "Sweeney-Cox_syndrome|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis|not_provided": 1,
    "Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis|not_provided": 7,
    "TWIST1-related_disorder|TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome": 2,
    "not_provided|TWIST1-related_craniosynostosis": 9,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|TWIST1-related_disorder": 1,
    "not_provided|TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome": 5,
    "not_provided|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis": 8,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|not_provided": 3,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|TWIST1-related_disorder|not_provided|Sweeney-Cox_syndrome": 1,
    "Saethre-Chotzen_syndrome|Coronal_craniosynostosis": 2,
    "Saethre-Chotzen_syndrome|Inborn_genetic_diseases": 1,
    "Sweeney-Cox_syndrome": 2,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|Sweeney-Cox_syndrome": 2,
    "TWIST1-related_craniosynostosis|Robinow-Sorauf_syndrome|Saethre-Chotzen_syndrome": 1,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|Sweeney-Cox_syndrome|Robinow-Sorauf_syndrome": 1,
    "Neurodevelopmental_delay|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis|not_provided": 1,
    "Inborn_genetic_diseases|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis": 1,
    "not_provided|Inborn_genetic_diseases|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis": 1,
    "TWIST1-related_disorder": 5,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|not_specified": 1,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|not_provided|not_specified": 1,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|TWIST1-related_disorder|Sweeney-Cox_syndrome": 1,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|Robinow-Sorauf_syndrome|Sweeney-Cox_syndrome|not_specified": 1,
    "not_provided|TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|TWIST1-related_disorder|not_specified": 1,
    "Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis|Robinow-Sorauf_syndrome": 1,
    "TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Sweeney-Cox_syndrome": 1,
    "not_specified|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis": 1,
    "not_specified|TWIST1-related_disorder|Robinow-Sorauf_syndrome|Sweeney-Cox_syndrome|Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis|not_provided": 1,
    "Saethre-Chotzen_syndrome|TWIST1-related_craniosynostosis|Saethre-Chotzen_syndrome_with_eyelid_anomalies": 1,
    "Preeclampsia|Gestational_diabetes_mellitus_uncontrolled": 2,
    "not_provided|SP8-related_disorder": 5,
    "SP8-related_disorder": 22,
    "not_specified|SP8-related_disorder": 2,
    "Cognitive_regression|Dyslexia|Attention_deficit_hyperactivity_disorder|Hip_dislocation|Delayed_speech_and_language_development|Seizure": 1,
    "SP4-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 95,
    "DNAH11-related_disorder": 26,
    "Primary_ciliary_dyskinesia|DNAH11-related_disorder": 51,
    "Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia|not_specified|not_provided": 2,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 11,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 33,
    "Primary_ciliary_dyskinesia_7": 135,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|not_provided": 4,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia": 23,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 29,
    "not_provided|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia|not_specified": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_7": 5,
    "Primary_ciliary_dyskinesia|See_cases": 1,
    "Primary_ciliary_dyskinesia|not_provided|Infertility_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia": 10,
    "Ciliary_dyskinesia|_primary|_37|Primary_ciliary_dyskinesia": 1,
    "DNAH11-related_disorder|not_provided|Primary_ciliary_dyskinesia": 7,
    "Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia|not_provided": 11,
    "Primary_ciliary_dyskinesia_7|not_provided": 4,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_7|not_specified": 1,
    "Primary_ciliary_dyskinesia|Laterality_defects|_autosomal_dominant": 1,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 2,
    "Primary_ciliary_dyskinesia_7|not_specified|not_provided|Primary_ciliary_dyskinesia": 4,
    "not_provided|DNAH11-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 2,
    "Primary_ciliary_dyskinesia_7|not_provided|Primary_ciliary_dyskinesia": 6,
    "Kartagener_syndrome|Primary_ciliary_dyskinesia_7": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|not_provided": 9,
    "not_specified|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia": 5,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|not_specified|not_provided": 3,
    "not_provided|DNAH11-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Situs_inversus|Primary_ciliary_dyskinesia": 1,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia|not_provided": 1,
    "DNAH11-related_disorder|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 7,
    "Primary_ciliary_dyskinesia|not_provided|DNAH11-related_disorder": 1,
    "Primary_ciliary_dyskinesia_7|DNAH11-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia_7": 7,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_7": 2,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_7": 6,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 1,
    "not_provided|DNAH11-related_disorder|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia": 1,
    "DNAH11-related_disorder|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 2,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia|not_provided": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|not_specified": 1,
    "Primary_ciliary_dyskinesia_7|not_specified": 1,
    "DNAH11-related_disorder|not_specified|Primary_ciliary_dyskinesia|not_provided": 1,
    "DNAH11-related_disorder|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia|not_specified": 1,
    "Primary_ciliary_dyskinesia_7|not_provided|Primary_ciliary_dyskinesia|not_specified": 1,
    "not_specified|Primary_ciliary_dyskinesia_7": 1,
    "Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia|DNAH11-related_disorder": 2,
    "Primary_ciliary_dyskinesia|DNAH11-related_disorder|not_provided|Primary_ciliary_dyskinesia_7": 1,
    "Primary_ciliary_dyskinesia|DNAH11-related_disorder|not_specified": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|not_specified": 5,
    "not_provided|Primary_ciliary_dyskinesia_7|not_specified|Primary_ciliary_dyskinesia": 2,
    "DNAH11-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7|DNAH11-related_disorder": 2,
    "Primary_ciliary_dyskinesia_7|not_specified|Primary_ciliary_dyskinesia": 2,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia_7|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|DNAH11-related_disorder": 2,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_7": 1,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_7": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_7|CILIARY_DYSKINESIA|_PRIMARY|_7|_WITH_SITUS_INVERSUS": 1,
    "not_specified|Primary_ciliary_dyskinesia_7|not_provided|Primary_ciliary_dyskinesia": 1,
    "Developmental_defect_during_embryogenesis|DNAH11-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_7": 1,
    "DNAH11-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia_3": 1,
    "Primary_ciliary_dyskinesia_7|DNAH11-related_disorder|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia|Male_infertility|Primary_ciliary_dyskinesia_7": 1,
    "DNAH11-related_disorder|Primary_ciliary_dyskinesia_7|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_7|Situs_inversus|Primary_ciliary_dyskinesia": 1,
    "IL6_POLYMORPHISM": 1,
    "Diabetes_mellitus|_type_1|_susceptibility_to|Diabetes_mellitus_type_2|_susceptibility_to|Kaposi_sarcoma|.|Crohn_disease-associated_growth_failure|_susceptibility_to|.|Cholangiocarcinoma": 1,
    "IL6-related_disorder|not_provided": 1,
    "IL6-related_disorder": 1,
    "TOMM7-related_early_onset_Leigh_disease": 1,
    "not_specified|Garg-Mishra_progeroid_syndrome": 1,
    "Garg-Mishra_progeroid_syndrome|See_cases": 1,
    "Hypomyelination_and_Congenital_Cataract|not_provided": 6,
    "Hypomyelination_and_Congenital_Cataract|HYCC1-related_disorder": 3,
    "HYCC1-related_disorder": 9,
    "Inborn_genetic_diseases|Hypomyelination_and_Congenital_Cataract": 12,
    "not_provided|Hypomyelination_and_Congenital_Cataract": 8,
    "Inborn_genetic_diseases|not_provided|Hypomyelination_and_Congenital_Cataract": 2,
    "Hypomyelination_and_Congenital_Cataract|Inborn_genetic_diseases": 4,
    "Hypomyelination_and_Congenital_Cataract|Inborn_genetic_diseases|HYCC1-related_disorder": 1,
    "not_provided|Hypomyelination_and_Congenital_Cataract|HYCC1-related_disorder": 1,
    "HYCC1-related_disorder|Hypomyelination_and_Congenital_Cataract|not_provided": 1,
    "Hypomyelination_and_Congenital_Cataract|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hypomyelination_and_Congenital_Cataract": 1,
    "Hypomyelination_and_Congenital_Cataract|not_specified|not_provided": 1,
    "HYCC1-related_disorder|not_provided": 1,
    "Hypomyelination_and_Congenital_Cataract|not_provided|HYCC1-related_disorder|not_specified": 1,
    "Tooth_agenesis|_selective|_X-linked|_1": 6,
    "not_specified|Hypomyelination_and_Congenital_Cataract": 1,
    "not_provided|HYCC1-related_disorder|Hypomyelination_and_Congenital_Cataract": 1,
    "PERCHING_syndrome": 13,
    "Bohring-Opitz_syndrome|PERCHING_syndrome": 1,
    "PERCHING_syndrome|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_42|not_provided": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_42": 1,
    "Retinitis_pigmentosa_42": 3,
    "Retinitis_pigmentosa_42|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_42": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_42": 1,
    "not_provided|KLHL7-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|PERCHING_syndrome": 1,
    "KLHL7-related_disorder|Retinitis_pigmentosa_42|PERCHING_syndrome": 2,
    "KLHL7-related_disorder": 2,
    "Distal_arthrogryposis|PERCHING_syndrome|Retinitis_pigmentosa_42|Ulnar_deviation_of_the_wrist": 1,
    "Retinitis_pigmentosa_42|not_provided|not_specified|PERCHING_syndrome": 1,
    "KLHL7-related_disorder|not_provided": 3,
    "PERCHING_syndrome|Bohring-Opitz-like_syndrome|Retinal_dystrophy|not_provided": 1,
    "PERCHING_syndrome|Cold-induced_sweating_syndrome_1": 3,
    "PERCHING_syndrome|Neurodevelopmental_delay|not_provided|KLHL7-related_disorder": 1,
    "Ulnar_deviation_of_the_wrist": 2,
    "PERCHING_syndrome|not_provided|Cold-induced_sweating_syndrome_1": 1,
    "GPNMB-related_disorder|not_provided": 3,
    "GPNMB-related_disorder": 7,
    "Amyloidosis|_primary_localized_cutaneous|_3": 14,
    "not_provided|GPNMB-related_disorder|Amyloidosis|_primary_localized_cutaneous|_3": 1,
    "not_provided|GPNMB-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|GPNMB-related_disorder": 1,
    "Primary_microcephaly": 7,
    "NPY_POLYMORPHISM|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5": 36,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5": 14,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_5": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|not_specified|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|GSDME-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5|not_specified": 6,
    "not_provided|GSDME-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|not_provided": 9,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|not_provided|not_specified": 3,
    "GSDME-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "GSDME-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5|GSDME-related_disorder|not_specified": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_5|not_provided": 2,
    "not_provided|GSDME-related_disorder": 1,
    "GSDME-related_disorder": 1,
    "Nonsyndromic_Hearing_Loss|_Mixed|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5|GSDME-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hearing_impairment|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_5|Inborn_genetic_diseases": 1,
    "Sensorineural_hearing_loss_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_5|Inborn_genetic_diseases": 1,
    "not_provided|GSDME-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_5": 1,
    "not_provided|Nonsyndromic_Hearing_Loss|_Mixed": 2,
    "GSDME-related_disorder|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "not_provided|Thrombocytopenia|Thrombocytopenia_4": 1,
    "Thrombocytopenia_4": 8,
    "CYCS-related_disorder": 2,
    "Thrombocytopenia_4|not_provided": 3,
    "not_provided|Thrombocytopenia": 13,
    "Thrombocytopenia|Thrombocytopenia_4": 1,
    "Thrombocytopenia_4|not_provided|not_specified": 1,
    "Keratoconus|not_provided": 1,
    "HNRNPA2B1-related_disorder": 9,
    "HNRNPA2B1-related_disorder|not_provided": 1,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 257,
    "Myopathy|_autophagic_vacuolar|_infantile-onset|Oculopharyngeal_muscular_dystrophy_2|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 1,
    "Oculopharyngeal_muscular_dystrophy_2": 3,
    "not_provided|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 7,
    "not_provided|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|HNRNPA2B1-related_disorder": 1,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|HNRNPA2B1-related_disorder": 11,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|not_provided": 5,
    "not_provided|HNRNPA2B1-related_disorder|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 1,
    "not_specified|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 2,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|Oculopharyngeal_muscular_dystrophy_2": 1,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|Inborn_genetic_diseases": 1,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|HNRNPA2B1-related_disorder|not_provided": 2,
    "HNRNPA2B1-related_disorder|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 3,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|not_specified|not_provided": 1,
    "HNRNPA2B1-related_disorder|not_provided|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 1,
    "not_specified|not_provided|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2": 1,
    "HNRNPA2B1-related_disorder|Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|not_provided": 1,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_2|not_provided|not_specified": 1,
    "Autosomal_recessive_osteopetrosis_8|not_provided": 3,
    "SNX10-related_disorder": 1,
    "not_provided|SNX10-related_disorder": 1,
    "Autosomal_recessive_osteopetrosis_8": 5,
    "not_provided|Autosomal_recessive_osteopetrosis_8": 1,
    "SNX10-related_disorder|not_provided": 4,
    "not_provided|Autosomal_recessive_osteopetrosis_8|SNX10-related_disorder": 1,
    "Autosomal_recessive_osteopetrosis_8|not_provided|Infantile_osteopetrosis": 1,
    "Human_HOXA1_syndromes": 21,
    "Bosley-Salih-Alorainy_syndrome": 20,
    "Bosley-Salih-Alorainy_syndrome|Human_HOXA1_syndromes": 1,
    "not_provided|Bosley-Salih-Alorainy_syndrome": 1,
    "HOXA1-related_disorder|Inborn_genetic_diseases": 1,
    "HOXA1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Bosley-Salih-Alorainy_syndrome": 1,
    "Inborn_genetic_diseases|Bosley-Salih-Alorainy_syndrome|not_provided|Intellectual_disability": 1,
    "Bosley-Salih-Alorainy_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|HOXA1-related_disorder": 2,
    "HOXA1-related_disorder|not_provided": 1,
    "Bilateral_microtia-deafness-cleft_palate_syndrome|not_provided|Inborn_genetic_diseases|Human_HOXA1_syndromes|Bosley-Salih-Alorainy_syndrome": 1,
    "Bosley-Salih-Alorainy_syndrome|HOXA1-related_disorder": 1,
    "Bilateral_microtia-deafness-cleft_palate_syndrome": 32,
    "Bosley-Salih-Alorainy_syndrome|Inborn_genetic_diseases|Human_HOXA1_syndromes": 1,
    "Bilateral_microtia-deafness-cleft_palate_syndrome|not_provided|HOXA1-related_disorder|Inborn_genetic_diseases|Human_HOXA1_syndromes|Bosley-Salih-Alorainy_syndrome": 1,
    "Human_HOXA1_syndromes|not_provided": 1,
    "Bosley-Salih-Alorainy_syndrome|Inborn_genetic_diseases|HOXA1-related_disorder": 1,
    "Bosley-Salih-Alorainy_syndrome|Human_HOXA1_syndromes|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Human_HOXA1_syndromes": 1,
    "not_provided|Human_HOXA1_syndromes": 1,
    "Bilateral_microtia-deafness-cleft_palate_syndrome|not_provided|Human_HOXA1_syndromes|Bosley-Salih-Alorainy_syndrome": 1,
    "HOXA2-related_disorder": 13,
    "Inborn_genetic_diseases|Bilateral_microtia-deafness-cleft_palate_syndrome": 3,
    "Bilateral_microtia-deafness-cleft_palate_syndrome|not_provided": 1,
    "Bilateral_microtia-deafness-cleft_palate_syndrome|not_provided|HOXA2-related_disorder": 1,
    "MICROTIA_WITH_OR_WITHOUT_HEARING_IMPAIRMENT": 1,
    "MICROTIA_WITHOUT_HEARING_IMPAIRMENT": 1,
    "Bilateral_microtia-deafness-cleft_palate_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Bilateral_microtia-deafness-cleft_palate_syndrome": 1,
    "HOXA2-related_disorder|Bilateral_microtia-deafness-cleft_palate_syndrome": 1,
    "not_specified|HOXA4-related_disorder": 1,
    "HOXA4-related_disorder": 5,
    "HOXA4-related_disorder|not_provided": 1,
    "Hand-foot-genital_syndrome": 11,
    "HOXA10-related_disorder": 9,
    "HOXA10-related_disorder|not_provided": 1,
    "not_provided|HOXA10-related_disorder": 1,
    "Mesomelic_dysplasia_with_urogenital_abnormalities": 1,
    "Inherited_genitourinary_tract_anomalies": 2,
    "HOXA11-related_disorder": 12,
    "HOXA11-related_disorder|not_specified": 3,
    "Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_1|not_provided": 2,
    "Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_1|not_specified": 2,
    "HOXA11-related_disorder|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_1": 1,
    "not_specified|HOXA11-related_disorder": 1,
    "Guttmacher_syndrome|Hand-foot-genital_syndrome": 28,
    "HOXA13-related_disorder": 16,
    "Inborn_genetic_diseases|Guttmacher_syndrome|Hand-foot-genital_syndrome": 5,
    "Inborn_genetic_diseases|HOXA13-related_disorder": 1,
    "Hand-foot-genital_syndrome|Guttmacher_syndrome|not_provided": 3,
    "not_provided|Guttmacher_syndrome|Hand-foot-genital_syndrome": 3,
    "not_provided|Hand-foot-genital_syndrome|Guttmacher_syndrome": 3,
    "Hand-foot-genital_syndrome|Guttmacher_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Guttmacher_syndrome|Hand-foot-genital_syndrome|not_provided": 1,
    "Guttmacher_syndrome|Hand-foot-genital_syndrome|not_provided": 4,
    "not_specified|HOXA13-related_disorder": 1,
    "HOXA13-related_disorder|not_provided": 1,
    "not_provided|HOXA13-related_disorder|Hand-foot-genital_syndrome|Guttmacher_syndrome": 2,
    "not_provided|HOXA13-related_disorder": 3,
    "Hand-foot-genital_syndrome|Guttmacher_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hand-foot-genital_syndrome|Guttmacher_syndrome|not_provided": 1,
    "HOXA13-related_disorder|Guttmacher_syndrome|Hand-foot-genital_syndrome|not_provided": 1,
    "HOXA13-related_disorder|Hand-foot-genital_syndrome|Guttmacher_syndrome": 1,
    "HIBADH-related_disorder": 1,
    "CHN2-related_disorder": 15,
    "CHN2-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 102,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 26,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype": 19,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "Cardiovascular_phenotype|FKBP14-related_disorder|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype|not_specified": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype|not_provided": 3,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_provided": 2,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "FKBP14-related_disorder|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Pes_valgus|Thoracolumbar_scoliosis|Congenital_muscular_dystrophy|Joint_hypermobility|Hypotonia": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Hypotonia": 1,
    "FKBP14-related_disorder|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "FKBP14-related_disorder|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_specified": 1,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "not_specified|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_provided|Cardiovascular_phenotype": 2,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 3,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "not_provided|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2": 1,
    "not_specified|Ehlers-Danlos_syndrome|_kyphoscoliotic_type|_2|Cardiovascular_phenotype": 1,
    "Distal_spinal_muscular_atrophy|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D": 2,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A": 3,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D": 5,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|Distal_spinal_muscular_atrophy|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Distal_spinal_muscular_atrophy|not_provided|Charcot-Marie-Tooth_disease_type_2D": 1,
    "Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D": 3,
    "Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided|Charcot-Marie-Tooth_disease_type_2D": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|Distal_spinal_muscular_atrophy": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy": 5,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D": 1,
    "not_provided|not_specified|GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Spinal_muscular_atrophy|_infantile|_James_type|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2D": 9,
    "not_provided|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D|not_specified": 1,
    "GARS-associated_growth_retardation_and_developmental_delay": 1,
    "Charcot-Marie-Tooth_disease_type_2D|not_provided|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2D|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy": 1,
    "Inborn_genetic_diseases|Spinal_muscular_atrophy|_infantile|_James_type": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease|GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "GARS1-related_disorder": 4,
    "Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|Distal_spinal_muscular_atrophy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_5A": 3,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Spinal_muscular_atrophy|_infantile|_James_type|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_specified|Spinal_muscular_atrophy|_infantile|_James_type|Charcot-Marie-Tooth_disease_type_2D|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "GARS1-related_neuropathies|Charcot-Marie-Tooth_disease_type_2|GARS-Associated_Axonal_Neuropathy": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|not_specified": 2,
    "Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|not_provided|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|not_specified|Charcot-Marie-Tooth_disease_type_2D|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5": 1,
    "Distal_spinal_muscular_atrophy|GARS1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2D": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_specified|GARS-associated_growth_retardation_and_developmental_delay": 1,
    "GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5|Hereditary_motor_neuron_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Spinal_muscular_atrophy|_infantile|_James_type": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|See_cases|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|not_provided|GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 2,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Spinal_muscular_atrophy|_infantile|_James_type|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_2D|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|GARS-Associated_Axonal_Neuropathy": 1,
    "not_provided|GARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D": 1,
    "Charcot-Marie-Tooth_disease_type_2|Parkinsonian_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2D|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|GARS1-related_disorder": 1,
    "not_specified|Charcot-Marie-Tooth_disease|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D": 1,
    "GARS1-related_disorder|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Pes_cavus|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|See_cases": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|GARS-Associated_Axonal_Neuropathy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_5": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Spinal_muscular_atrophy|_infantile|_James_type": 2,
    "Spinal_muscular_atrophy|_infantile|_James_type|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "GARS1-related_disorder|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2D|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Spinal_muscular_atrophy|_infantile|_James_type|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D|Charcot-Marie-Tooth_disease|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|not_specified|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2D": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2D|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|GARS1-related_disorder": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Peripheral_axonal_neuropathy|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2": 2,
    "Peripheral_axonal_neuropathy|not_provided|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2": 2,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2D|Distal_spinal_muscular_atrophy": 1,
    "not_specified|Prostate_cancer": 7,
    "Colton-null_phenotype": 1,
    "COLTON_BLOOD_GROUP_POLYMORPHISM|not_provided": 1,
    "not_provided|AQP1-related_disorder": 3,
    "AQP1-related_disorder|not_provided": 1,
    "AQP1-related_pulmonary_hypertension": 1,
    "AQP1-related_disorder": 3,
    "Isolated_growth_hormone_deficiency_type_IB": 20,
    "Isolated_growth_hormone_deficiency|_type_4": 13,
    "not_provided|Isolated_growth_hormone_deficiency_type_IB": 9,
    "Isolated_growth_hormone_deficiency_type_IB|not_provided": 9,
    "not_provided|not_specified|Isolated_growth_hormone_deficiency_type_IB": 1,
    "Isolated_growth_hormone_deficiency|_type_4|not_provided": 4,
    "GHRHR-related_disorder|not_specified|Isolated_growth_hormone_deficiency_type_IB|not_provided|Idiopathic_growth_hormone_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Isolated_growth_hormone_deficiency_type_IB": 1,
    "Isolated_growth_hormone_deficiency_type_IB|Inborn_genetic_diseases": 1,
    "not_provided|GHRHR-related_disorder|Isolated_growth_hormone_deficiency_type_IB": 2,
    "Isolated_growth_hormone_deficiency|_type_4|not_provided|Isolated_growth_hormone_deficiency_type_IB": 1,
    "not_provided|Isolated_growth_hormone_deficiency_type_IB|Inborn_genetic_diseases": 1,
    "GHRHR-related_disorder|Isolated_growth_hormone_deficiency_type_IB|Idiopathic_growth_hormone_deficiency|not_provided": 1,
    "not_provided|Idiopathic_growth_hormone_deficiency|Isolated_growth_hormone_deficiency_type_IB": 1,
    "not_provided|Isolated_growth_hormone_deficiency|_type_4": 5,
    "Isolated_congenital_growth_hormone_deficiency": 2,
    "not_provided|Inborn_genetic_diseases|Isolated_growth_hormone_deficiency_type_IB": 1,
    "Inborn_genetic_diseases|GHRHR-related_disorder|not_provided": 1,
    "not_provided|Isolated_growth_hormone_deficiency_type_IB|Idiopathic_growth_hormone_deficiency": 1,
    "Inborn_genetic_diseases|Isolated_growth_hormone_deficiency_type_IB": 1,
    "Isolated_growth_hormone_deficiency_type_IB|not_specified|not_provided": 1,
    "Isolated_growth_hormone_deficiency_type_IB|not_provided|not_specified": 1,
    "Isolated_growth_hormone_deficiency_type_IB|not_provided|GHRHR-related_disorder|not_specified": 1,
    "GHRHR-related_disorder|not_provided": 1,
    "not_specified|not_provided|GHRHR-related_disorder": 1,
    "not_provided|Isolated_growth_hormone_deficiency_type_IB|GHRHR-related_disorder": 1,
    "Inborn_genetic_diseases|Isolated_growth_hormone_deficiency|_type_4": 1,
    "not_provided|Isolated_growth_hormone_deficiency_type_IB|not_specified": 1,
    "GHRHR-related_disorder": 1,
    "Hypercholesterolemia|_familial|_1|not_specified": 8,
    "Hypercholesterolemia": 3,
    "PDE1C-related_disorder": 22,
    "Hearing_loss|_autosomal_dominant_74": 7,
    "not_provided|PDE1C-related_disorder": 4,
    "not_provided|Hearing_loss|_autosomal_dominant_74": 4,
    "PDE1C-related_disorder|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss|Hearing_loss|_autosomal_dominant_74": 1,
    "Hearing_loss|_autosomal_dominant_74|not_provided": 2,
    "not_specified|Hearing_loss|_autosomal_dominant_74|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency": 32,
    "Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency|not_specified|not_provided": 1,
    "not_provided|Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency": 9,
    "Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency|not_provided": 4,
    "not_specified|Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency": 1,
    "Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency|not_specified": 5,
    "not_specified|Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency|not_provided": 1,
    "NT5C3A-related_disorder|Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency": 1,
    "NT5C3A-related_disorder": 1,
    "Hemolytic_anemia_due_to_pyrimidine_5'_nucleotidase_deficiency|NT5C3A-related_disorder": 1,
    "Retinitis_Pigmentosa|_Dominant|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa_9": 1,
    "Retinitis_pigmentosa_9": 5,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_9": 1,
    "RP9-related_disorder": 2,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_9": 1,
    "not_provided|Retinitis_pigmentosa_9": 1,
    "not_provided|Retinitis_pigmentosa_9|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_9": 1,
    "Bardet-Biedl_syndrome_9": 141,
    "not_provided|Bardet-Biedl_syndrome_9": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|BBS9-related_disorder": 8,
    "Bardet-Biedl_syndrome|BBS9-related_disorder|Bardet-Biedl_syndrome_9": 8,
    "BBS9-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 9,
    "BBS9-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_9": 4,
    "BBS9-related_disorder": 71,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|not_specified": 3,
    "BBS9-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 40,
    "Bardet-Biedl_syndrome|BBS9-related_disorder": 32,
    "BBS9-related_disorder|Bardet-Biedl_syndrome": 32,
    "BBS9-related_ciliopathy": 2,
    "Bardet-Biedl_syndrome_9|BBS9-related_disorder|Bardet-Biedl_syndrome": 8,
    "Bardet-Biedl_syndrome|BBS9-related_disorder|Bardet-Biedl_syndrome_9|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|BBS9-related_disorder": 5,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 42,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome_9|BBS9-related_disorder|Bardet-Biedl_syndrome|Retinal_vascular_dystrophy": 1,
    "not_specified|Bardet-Biedl_syndrome_9|not_provided": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_9": 2,
    "Bardet-Biedl_syndrome|BBS9-related_disorder|not_provided": 2,
    "BBS9-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 2,
    "BBS9-related_disorder|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|not_provided": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_9|BBS9-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|BBS9-related_disorder": 1,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 4,
    "Bardet-Biedl_syndrome_9|not_provided|not_specified|Bardet-Biedl_syndrome": 1,
    "BBS9-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 3,
    "Bardet-Biedl_syndrome|not_provided|not_specified|Bardet-Biedl_syndrome_9": 2,
    "BBS9-related_ciliopathy|Bardet-Biedl_syndrome|BBS9-related_disorder|Bardet-Biedl_syndrome_9|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|BBS9-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|BBS9-related_disorder|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_9|not_provided|Bardet-Biedl_syndrome": 2,
    "BBS9-related_disorder|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Abnormality_of_the_eye|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|BBS9-related_disorder|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome_9|BBS9-related_disorder": 3,
    "BBS9-related_disorder|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 5,
    "BBS9-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome|BBS9-related_disorder|Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|BBS9-related_disorder|not_specified": 2,
    "not_provided|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome|not_specified|not_provided|Bardet-Biedl_syndrome_9": 2,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "BBS9-related_disorder|Bardet-Biedl_syndrome_9|not_provided|Bardet-Biedl_syndrome": 1,
    "BBS9-related_ciliopathy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|BBS9-related_ciliopathy|BBS9-related_disorder|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome_9": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|BBS9-related_disorder": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_9|not_provided": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome_9|not_provided": 5,
    "BBS9-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|not_specified": 1,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_9|not_provided": 1,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases": 1,
    "BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome_9|BBS9-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS9-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_9|not_provided": 1,
    "BBS9-related_disorder|Bardet-Biedl_syndrome_9|not_specified|Bardet-Biedl_syndrome|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|BBS9-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome_9|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS9-related_disorder": 1,
    "BBS9-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 3,
    "BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome_1|not_specified|Bardet-Biedl_syndrome": 1,
    "BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome_9|not_specified|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_9": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|BBS9-related_ciliopathy|BBS9-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|BBS9-related_disorder": 1,
    "Bardet-Biedl_syndrome|Abnormality_of_the_eye|Bardet-Biedl_syndrome_9": 1,
    "BBS9-related_disorder|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome|Nephronophthisis_4|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|BBS9-related_disorder|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS9-related_disorder|Bardet-Biedl_syndrome_9|not_provided|Retinal_dystrophy": 1,
    "BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|Inborn_genetic_diseases|BBS9-related_disorder": 1,
    "not_specified|Bardet-Biedl_syndrome|Inborn_genetic_diseases|not_provided|BBS9-related_disorder": 1,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|BBS9-related_ciliopathy": 1,
    "Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|BBS9-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Bardet-Biedl_syndrome|BBS9-related_disorder": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|not_specified": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|BBS9-related_disorder": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_9|not_specified": 1,
    "Retinal_dystrophy|not_provided|BBS9-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "not_provided|BBS9-related_disorder|Bardet-Biedl_syndrome_9|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|BBS9-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|not_specified|BBS9-related_disorder": 1,
    "Inborn_genetic_diseases|BBS9-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS9-related_disorder": 1,
    "BBS9-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9": 1,
    "not_provided|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_9|Inborn_genetic_diseases|BBS9-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome|BBS9-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_9|Optic_atrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS9-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome_9|not_provided|BBS9-related_disorder|Bardet-Biedl_syndrome": 1,
    "BBS9-related_disorder|not_provided|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|not_provided|not_specified|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome|BBS9-related_disorder": 1,
    "not_provided|BBS9-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_9|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_9": 1,
    "Diaphanospondylodysostosis": 85,
    "BMPER-related_disorder": 4,
    "BMPER-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|Diaphanospondylodysostosis": 3,
    "not_provided|Diaphanospondylodysostosis": 25,
    "not_specified|not_provided|Diaphanospondylodysostosis": 1,
    "Diaphanospondylodysostosis|not_provided|Inborn_genetic_diseases": 1,
    "Diaphanospondylodysostosis|not_provided": 10,
    "Diaphanospondylodysostosis|Inborn_genetic_diseases|not_provided": 2,
    "Diaphanospondylodysostosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Diaphanospondylodysostosis": 1,
    "not_provided|Diaphanospondylodysostosis|BMPER-related_disorder": 1,
    "Inborn_genetic_diseases|Diaphanospondylodysostosis|not_provided": 1,
    "Asthma-related_traits|_susceptibility_to|_2": 1,
    "Atrial_septal_defect_4": 17,
    "Cardiovascular_phenotype|TBX20-related_disorder": 1,
    "not_provided|Atrial_septal_defect_4|Cardiovascular_phenotype": 3,
    "Atrial_septal_defect_4|not_provided|Cardiovascular_phenotype": 4,
    "TBX20-related_disorder|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|Atrial_septal_defect_4": 3,
    "not_specified|Atrial_septal_defect_4|Cardiovascular_phenotype|not_provided": 1,
    "Atrial_septal_defect_4|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Cardiovascular_phenotype|not_specified|Atrial_septal_defect_4": 1,
    "Wolff-Parkinson-White_pattern|Hypoplastic_right_heart_syndrome|Hypoplastic_left_heart_syndrome": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Atrial_septal_defect_4": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_4|not_provided": 2,
    "Atrial_septal_defect_4|not_provided": 3,
    "not_provided|TBX20-related_disorder|Cardiovascular_phenotype": 2,
    "TBX20-related_disorder": 2,
    "TBX20-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Atrial_septal_defect_4": 1,
    "Left_ventricular_noncompaction|not_provided": 1,
    "Atrial_septal_defect_4|Cardiovascular_phenotype|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1": 38,
    "not_specified|not_provided|TBX20-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_septal_defect_4": 1,
    "TBX20-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Atrial_septal_defect_4|not_provided|Aortic_valve_disease_1": 1,
    "not_provided|Cardiovascular_phenotype|TBX20-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|TBX20-related_disorder": 1,
    "not_provided|TBX20-related_disorder": 1,
    "Aortic_valve_disease_1|Atrial_septal_defect_4|not_provided": 1,
    "Atrial_septal_defect_4|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_8": 16,
    "ANLN-related_disorder": 8,
    "Focal_segmental_glomerulosclerosis_8|not_specified": 2,
    "Focal_segmental_glomerulosclerosis_8|not_provided": 18,
    "ANLN-related_disorder|not_provided": 11,
    "not_provided|Focal_segmental_glomerulosclerosis_8": 11,
    "not_specified|not_provided|ANLN-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_8|not_specified|not_provided": 1,
    "ANLN-related_disorder|not_specified|not_provided": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_8|not_specified": 2,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_8": 3,
    "not_provided|ANLN-related_disorder": 6,
    "not_specified|ANLN-related_disorder|Focal_segmental_glomerulosclerosis_8|not_provided": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_8": 1,
    "Focal_segmental_glomerulosclerosis_8|not_provided|not_specified": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_8|not_provided": 1,
    "Nephrotic_syndrome|not_specified|not_provided": 2,
    "not_provided|not_specified|ANLN-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_8|ANLN-related_disorder|not_provided": 1,
    "Primary_ciliary_dyskinesia_6": 207,
    "NME8-related_disorder|Primary_ciliary_dyskinesia_6|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_6|not_specified": 6,
    "Primary_ciliary_dyskinesia_6|Primary_ciliary_dyskinesia": 35,
    "not_specified|Primary_ciliary_dyskinesia_6": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 20,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_6": 3,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 4,
    "Primary_ciliary_dyskinesia|NME8-related_disorder|Primary_ciliary_dyskinesia_6": 2,
    "Primary_ciliary_dyskinesia_6|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_6|Primary_ciliary_dyskinesia|NME8-related_disorder": 2,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 4,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_6": 1,
    "NME8-related_disorder|Primary_ciliary_dyskinesia_6": 1,
    "NME8-related_disorder|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 2,
    "NME8-related_disorder": 3,
    "not_provided|Primary_ciliary_dyskinesia_6": 1,
    "not_provided|Primary_ciliary_dyskinesia_6|not_specified|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_6|NME8-related_disorder": 1,
    "not_specified|Primary_ciliary_dyskinesia_6|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia_6|not_specified": 1,
    "NME8-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6|not_specified": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia_6": 1,
    "Primary_ciliary_dyskinesia|NME8-related_disorder|Primary_ciliary_dyskinesia_6|not_provided": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_6": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_6": 1,
    "Primary_ciliary_dyskinesia_6|Primary_ciliary_dyskinesia|not_provided": 1,
    "Pyle_metaphyseal_dysplasia|not_provided|SFRP4-related_disorder": 1,
    "SFRP4-related_disorder|Pyle_metaphyseal_dysplasia|not_provided": 1,
    "not_provided|SFRP4-related_disorder": 2,
    "not_provided|Pyle_metaphyseal_dysplasia|SFRP4-related_disorder": 2,
    "Pyle_metaphyseal_dysplasia": 7,
    "Pyle_metaphyseal_dysplasia|not_provided": 1,
    "not_provided|Pyle_metaphyseal_dysplasia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_29|Inborn_genetic_diseases": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive_29": 12,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_29": 1,
    "VPS41-related_condition": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_29|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Wilms_tumor_5": 7,
    "not_specified|Hypogonadotropic_hypogonadism": 2,
    "POU6F2-related_disorder": 13,
    "not_provided|POU6F2-related_disorder": 3,
    "not_specified|POU6F2-related_disorder": 2,
    "POU6F2-related_disorder|not_provided": 1,
    "POU6F2-related_disorder|not_provided|Hypogonadotropic_hypogonadism": 1,
    "Hiatt-Neu-Cooper_neurodevelopmental_syndrome": 10,
    "Hiatt-Neu-Cooper_neurodevelopmental_syndrome|Intellectual_disability|Inborn_genetic_diseases|not_provided": 1,
    "RALA-related_disorder|not_provided": 2,
    "RALA-related_disorder": 1,
    "CDK13-related_disorder": 19,
    "Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 69,
    "Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|not_provided": 17,
    "not_provided|CDK13-related_disorder": 14,
    "not_provided|Inborn_genetic_diseases|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 2,
    "Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 12,
    "CDK13-related_disorder|Inborn_genetic_diseases|not_provided|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 1,
    "Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|not_provided|Inborn_genetic_diseases": 3,
    "Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|Inborn_genetic_diseases|not_provided": 2,
    "CDK13-related_disorder|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|CDK13-related_disorder": 1,
    "CDK13-related_disorder|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|CDK13-related_disorder": 1,
    "CDK13-related_disorder|not_provided|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 1,
    "Inborn_genetic_diseases|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|not_provided": 3,
    "not_specified|Intellectual_disability|not_provided|Inborn_genetic_diseases": 2,
    "CDK13-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "CDK13-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Heart|_malformation_of": 2,
    "Global_developmental_delay|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|Inborn_genetic_diseases|not_provided|Autism_spectrum_disorder": 1,
    "not_provided|not_specified|CDK13-related_disorder|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 1,
    "CDK13-related_disorder|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 1,
    "Marfanoid_habitus_and_intellectual_disability|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder|Inborn_genetic_diseases|not_provided|Global_developmental_delay": 1,
    "Neurodevelopmental_abnormality|Congenital_heart_defects|_dysmorphic_facial_features|_and_intellectual_developmental_disorder": 1,
    "not_provided|Syndromic_intellectual_disability|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability": 4,
    "not_provided|CDK13-related_disorder|Inborn_genetic_diseases": 1,
    "Wolfram-like_disorder|not_provided": 1,
    "CDK13-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Trichothiodystrophy_1|_photosensitive": 13,
    "Trichothiodystrophy_4|_nonphotosensitive|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Trichothiodystrophy_4|_nonphotosensitive": 3,
    "Trichothiodystrophy_4|_nonphotosensitive": 8,
    "Trichothiodystrophy_4|_nonphotosensitive|not_provided": 1,
    "MPLKIP-related_disorder|not_provided": 1,
    "not_provided|MPLKIP-related_disorder": 1,
    "MPLKIP-related_disorder": 1,
    "Glutaryl-CoA_oxidase_deficiency": 6,
    "SUGCT-related_disorder": 1,
    "not_specified|SUGCT-related_disorder|not_provided": 1,
    "SUGCT-related_disorder|not_provided": 2,
    "not_provided|Glutaryl-CoA_oxidase_deficiency|SUGCT-related_disorder": 1,
    "Glutaryl-CoA_oxidase_deficiency|not_specified": 2,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 370,
    "Polydactyly|not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|Pallister-Hall_syndrome": 14,
    "not_provided|Greig_cephalopolysyndactyly_syndrome|Polydactyly|Pallister-Hall_syndrome": 5,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly": 6,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome": 19,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|not_provided": 2,
    "not_provided|Greig_cephalopolysyndactyly_syndrome|Polydactyly": 1,
    "not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly": 2,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly": 27,
    "Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 18,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly": 10,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 10,
    "Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided": 2,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|not_provided|Pallister-Hall_syndrome": 3,
    "Polydactyly|not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 2,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|not_provided": 1,
    "Pallister-Hall_syndrome|not_specified|not_provided|Greig_cephalopolysyndactyly_syndrome|Polydactyly": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|Polydactyly": 1,
    "not_provided|GLI3-related_disorder": 2,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|GLI3-related_disorder": 4,
    "Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 102,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|GLI3-related_disorder": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 252,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 104,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_specified": 1,
    "GLI3-related_disorder": 52,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|GLI3-related_disorder|Inborn_genetic_diseases": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Pallister-Hall_syndrome": 14,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases": 13,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|not_provided": 2,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|not_specified|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|GLI3-related_disorder": 6,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4": 8,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 3,
    "Polydactyly|_postaxial|_type_A1": 15,
    "not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 5,
    "Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|GLI3-related_disorder": 1,
    "Greig_cephalopolysyndactyly_syndrome": 26,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 2,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|not_provided": 2,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 5,
    "Cronkhite-Canada_syndrome": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided": 1,
    "GLI3-related_disorder|Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|not_provided": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Intellectual_disability": 1,
    "not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 9,
    "Inborn_genetic_diseases|Polydactyly|Pallister-Hall_syndrome|Dystonia|_early-onset|_and/or_spastic_paraplegia|Greig_cephalopolysyndactyly_syndrome": 1,
    "Postaxial_polydactyly_type_B|Postaxial_polydactyly_type_A": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 1,
    "Pallister-Hall_syndrome|Polydactyly|Greig_cephalopolysyndactyly_syndrome": 3,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_provided": 2,
    "Greig_cephalopolysyndactyly_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 9,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Inborn_genetic_diseases": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome": 11,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided": 11,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided": 5,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|not_provided|Polydactyly": 1,
    "Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|not_provided": 4,
    "Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 2,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|not_specified|not_provided": 3,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|not_provided|not_specified|Polydactyly": 1,
    "GLI3-related_disorder|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|not_provided": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|not_provided": 1,
    "Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 4,
    "Pallister-Hall_syndrome|GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Polydactyly": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Pallister-Hall_syndrome|not_provided|Greig_cephalopolysyndactyly_syndrome|not_specified|Polydactyly": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified": 4,
    "Pallister-Hall_syndrome|GLI3-related_disorder|Polydactyly|Greig_cephalopolysyndactyly_syndrome|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 13,
    "Postaxial_polydactyly|_type_A1/B": 2,
    "not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|not_provided|not_specified": 1,
    "Polysyndactyly_4": 3,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Polydactyly": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases|Polydactyly": 1,
    "Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome": 1,
    "not_provided|Polydactyly|_postaxial|_type_A1|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Pallister-Hall_syndrome|Polydactyly": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Inborn_genetic_diseases|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|GLI3-related_disorder": 1,
    "GLI3-related_disorder|not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "polysyndactyly": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_provided": 1,
    "GLI3-related_disorder|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided": 1,
    "not_specified|Greig_cephalopolysyndactyly_syndrome|Hamartoma_of_hypothalamus|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Polydactyly": 3,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases": 4,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|not_provided": 2,
    "Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "GLI3-related_disorder|not_provided|not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly": 1,
    "not_provided|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Inborn_genetic_diseases": 2,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|not_specified": 1,
    "Pallister-Hall_syndrome|not_specified|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases|not_provided|Polydactyly": 1,
    "Pallister-Hall_syndrome|not_provided|Greig_cephalopolysyndactyly_syndrome|Polydactyly|Polydactyly|_postaxial|_type_A1|Hamartoma_of_hypothalamus|Polysyndactyly_4": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Polydactyly": 1,
    "not_specified|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases|GLI3-related_disorder": 1,
    "Polydactyly|not_specified|not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 1,
    "Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|not_specified|not_provided": 1,
    "Polydactyly|not_specified|not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|GLI3-related_disorder|Pallister-Hall_syndrome": 1,
    "Inborn_genetic_diseases|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 2,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified|GLI3-related_disorder": 1,
    "Pallister-Hall_syndrome|GLI3-related_disorder|not_provided|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases|Polydactyly|not_specified": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided|not_specified|Polydactyly|Polysyndactyly_4": 1,
    "GLI3-related_disorder|not_provided": 3,
    "GLI3-related_disorder|Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 1,
    "Polydactyly|Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome": 1,
    "GLI3-related_disorder|Inborn_genetic_diseases": 2,
    "Pallister-Hall_syndrome|Polydactyly|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|not_provided|not_specified": 1,
    "Greig_cephalopolysyndactyly_syndrome|_severe": 1,
    "not_provided|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 2,
    "Congenital_diaphragmatic_hernia": 4,
    "Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1": 2,
    "Inborn_genetic_diseases|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 2,
    "Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|not_provided": 2,
    "Pallister-Hall_syndrome|not_specified|Greig_cephalopolysyndactyly_syndrome|Polydactyly|not_provided": 1,
    "not_provided|Polydactyly|_postaxial|_type_A1": 1,
    "not_provided|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome": 1,
    "Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Inborn_genetic_diseases": 1,
    "Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases": 1,
    "Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_provided|not_specified": 1,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|GLI3-related_disorder|Polysyndactyly_4|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1": 1,
    "GLI3-related_disorder|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|not_provided": 1,
    "not_provided|not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 1,
    "Postaxial_polydactyly_type_B": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_specified": 1,
    "not_provided|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome": 1,
    "GLI3-related_disorder|Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 4,
    "Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 1,
    "Postaxial_polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|not_specified|not_provided|Postaxial_polydactyly|_type_A1/B": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Pallister-Hall_syndrome|not_provided|Greig_cephalopolysyndactyly_syndrome|Polydactyly|not_specified": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified": 1,
    "not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 3,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|GLI3-related_disorder": 1,
    "not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified": 3,
    "Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|GLI3-related_disorder": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Inborn_genetic_diseases|Generalized_dystonia|Macrocephaly|Global_developmental_delay|Functional_motor_deficit|not_provided": 1,
    "not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases": 1,
    "Pallister-Hall_syndrome|Polydactyly|not_provided|Greig_cephalopolysyndactyly_syndrome": 1,
    "Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4": 2,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Inborn_genetic_diseases": 1,
    "Abnormality_of_prenatal_development_or_birth|GLI3-related_disorder|Postaxial_polydactyly|_type_A1/B": 1,
    "not_provided|Polydactyly|_postaxial|_type_A1|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4": 1,
    "Polydactyly|not_provided|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified|not_provided": 1,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_specified": 1,
    "Basilar_invagination|Short_palpebral_fissure|Babinski_sign|Hyperreflexia|Ptosis|Polysyndactyly_of_hallux|Umbilical_hernia|Postaxial_hand_polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hand_polydactyly": 1,
    "Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Polydactyly|not_provided": 1,
    "GLI3-related_postaxial_polydactyly|Disorder_of_sexual_differentiation": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided|Polydactyly|not_specified": 1,
    "Polydactyly|Pallister-Hall_syndrome|GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome": 1,
    "Polydactyly|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided": 1,
    "GLI3-related_disorder|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 2,
    "not_specified|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|GLI3-related_disorder": 3,
    "not_specified|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_provided": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|Polydactyly|not_provided|Polysyndactyly_4": 1,
    "Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|GLI3-related_disorder": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome": 1,
    "not_provided|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4": 1,
    "not_specified|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 2,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified": 3,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|GLI3-related_disorder|not_provided": 1,
    "not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|Inborn_genetic_diseases": 1,
    "not_specified|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1": 1,
    "Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|not_provided": 1,
    "not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 2,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Polydactyly|not_specified": 1,
    "Pallister-Hall_syndrome|not_specified|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Polydactyly|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polydactyly": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified|GLI3-related_disorder": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Inborn_genetic_diseases|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome": 1,
    "not_provided|Pallister-Hall_syndrome|Polydactyly|Greig_cephalopolysyndactyly_syndrome": 1,
    "Polydactyly|not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "not_provided|GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome": 2,
    "Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|not_provided|Polydactyly|not_specified": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4": 1,
    "not_provided|GLI3-related_disorder|Polydactyly|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_provided|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Inborn_genetic_diseases|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome": 1,
    "Polydactyly|Inborn_genetic_diseases|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided": 1,
    "GLI3-related_disorder|not_specified|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1": 1,
    "Polydactyly|not_specified|GLI3-related_disorder|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_specified|Polydactyly|not_provided": 1,
    "not_specified|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|not_provided|Polydactyly": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|not_provided": 3,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|not_specified": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polydactyly|not_specified|GLI3-related_disorder": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Inborn_genetic_diseases": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|not_specified": 1,
    "Intellectual_disability|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|not_specified|not_provided": 1,
    "GLI3-related_disorder|Polydactyly|_postaxial|_type_A1|Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Pallister-Hall_syndrome|not_specified|not_provided|Polydactyly": 1,
    "Polydactyly|not_provided|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polydactyly|not_specified": 1,
    "not_provided|Hepatoblastoma|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1": 1,
    "Pallister-Hall_syndrome|Greig_cephalopolysyndactyly_syndrome|Polydactyly|not_provided|Inborn_genetic_diseases|Polydactyly|_postaxial|_type_A1|Hamartoma_of_hypothalamus|Polysyndactyly_4": 1,
    "Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|GLI3-related_disorder|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4": 1,
    "Hepatoblastoma|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1": 1,
    "Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polysyndactyly_4|Greig_cephalopolysyndactyly_syndrome|not_specified|not_provided": 1,
    "GLI3-related_disorder|Greig_cephalopolysyndactyly_syndrome|Pallister-Hall_syndrome|Polydactyly|_postaxial|_type_A1|Polysyndactyly_4|not_provided": 1,
    "Greig_cephalopolysyndactyly_syndrome|Polysyndactyly_4|Polydactyly|_postaxial|_type_A1|Pallister-Hall_syndrome|Polydactyly|not_specified|not_provided": 1,
    "Hyperbiliverdinemia": 4,
    "BLVRA-related_disorder": 1,
    "Hyperbiliverdinemia|not_provided": 1,
    "BLVRA-related_disorder|not_provided": 4,
    "Hyperbiliverdinemia|not_specified": 1,
    "Glycogen_storage_disease_type_X": 100,
    "Glycogen_storage_disease_type_X|PGAM2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_type_X": 10,
    "Glycogen_storage_disease_type_X|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Glycogen_storage_disease_type_X|PGAM2-related_disorder": 1,
    "Rhabdomyolysis": 2,
    "not_provided|Glycogen_storage_disease_type_X": 10,
    "Glycogen_storage_disease_type_X|Inborn_genetic_diseases": 8,
    "Glycogen_storage_disease_type_X|not_specified": 2,
    "not_provided|Glycogen_storage_disease_type_X|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_type_X": 1,
    "not_provided|PGAM2-related_disorder|Glycogen_storage_disease_type_X": 1,
    "PGAM2-related_disorder|Inborn_genetic_diseases|Glycogen_storage_disease_type_X": 1,
    "Glycogen_storage_disease_type_X|not_provided": 3,
    "Glycogen_storage_disease_type_X|PGAM2-related_disorder": 2,
    "not_provided|PGAM2-related_disorder|not_specified|Glycogen_storage_disease_type_X": 1,
    "PGAM2-related_disorder": 2,
    "not_provided|not_specified|Glycogen_storage_disease_type_X": 1,
    "not_specified|Glycogen_storage_disease_type_X": 1,
    "PGAM2-related_disorder|Glycogen_storage_disease_type_X|not_provided": 2,
    "not_provided|Glycogen_storage_disease_type_X|not_specified": 1,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_type_X": 1,
    "AEBP1-related_disorder": 5,
    "AEBP1-related_disorder|not_provided": 12,
    "Ehlers-Danlos_syndrome|_classic-like|_2": 10,
    "not_specified|Ehlers-Danlos_syndrome|_classic-like|_2": 1,
    "AEBP1-related_disorder|not_provided|not_specified": 1,
    "not_provided|AEBP1-related_disorder": 13,
    "not_provided|Ehlers-Danlos_syndrome|_classic-like|_2": 6,
    "Ehlers-Danlos_syndrome|_classic-like|_2|not_provided": 8,
    "AEBP1-related_disorder|not_specified|not_provided": 1,
    "not_provided|AEBP1-related_disorder|not_specified": 2,
    "Ehlers-Danlos_syndrome|_classic-like|_2|not_specified|not_provided": 1,
    "not_specified|AEBP1-related_disorder|not_provided": 1,
    "Autism_spectrum_disorder|Ehlers-Danlos_syndrome|_classic-like|_2": 1,
    "not_specified|not_provided|AEBP1-related_disorder": 1,
    "not_provided|not_specified|AEBP1-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Transient_Neonatal_Diabetes|_Recessive": 4,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Transient_Neonatal_Diabetes|_Recessive": 2,
    "Hyperinsulinism|_Dominant|Maturity_onset_diabetes_mellitus_in_young|not_provided|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Transient_Neonatal_Diabetes|_Recessive": 2,
    "Hyperinsulinism_due_to_glucokinase_deficiency|not_provided|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 22,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Recessive|not_specified|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Hyperinsulinism_due_to_glucokinase_deficiency|Transient_Neonatal_Diabetes|_Recessive|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2": 58,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2": 6,
    "Monogenic_diabetes|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 2,
    "Hyperinsulinism_due_to_glucokinase_deficiency|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity-onset_diabetes_of_the_young_type_1|not_provided": 1,
    "not_provided|Hyperinsulinism_due_to_glucokinase_deficiency": 2,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2": 9,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Monogenic_diabetes": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 15,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|not_provided": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_2": 18,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2": 4,
    "Familial_hyperinsulinism": 4,
    "Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes": 7,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency": 2,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|not_provided": 12,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2": 3,
    "not_specified|Monogenic_diabetes|not_provided": 6,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided": 13,
    "Inborn_genetic_diseases|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|not_provided|Monogenic_diabetes": 3,
    "GCK-related_disorder|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|not_provided": 17,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_specified": 5,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young": 11,
    "Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Monogenic_diabetes": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young": 15,
    "Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_provided": 4,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 27,
    "Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 5,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes": 17,
    "GCK-related_disorder|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "not_provided|GCK-related_disorder": 2,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 8,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2": 27,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive": 3,
    "GCK-related_disorder|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Recessive|Hyperinsulinism_due_to_glucokinase_deficiency": 6,
    "Hyperinsulinism_due_to_glucokinase_deficiency|not_specified|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Transient_Neonatal_Diabetes|_Recessive": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2": 8,
    "GCK-related_disorder": 17,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|GCK-related_disorder|not_provided": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified|GCK-related_disorder": 1,
    "GCK-related_disorder|Monogenic_diabetes|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2|not_specified": 1,
    "Monogenic_diabetes|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_2": 4,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2": 4,
    "GCK-related_disorder|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 1,
    "not_provided|GCK-related_disorder|Monogenic_diabetes": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes": 6,
    "Hyperinsulinism_due_to_glucokinase_deficiency": 4,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes|not_provided|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 8,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Monogenic_diabetes": 1,
    "GCK-related_disorder|Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young": 10,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes|not_specified": 2,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_provided|not_specified": 2,
    "not_provided|not_specified|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|not_provided|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus|Monogenic_diabetes": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 3,
    "not_provided|Monogenic_diabetes|not_specified": 2,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2|not_specified": 1,
    "not_provided|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 12,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|not_specified": 1,
    "Monogenic_diabetes|not_provided|Gestational_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 21,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young": 3,
    "Transient_Neonatal_Diabetes|_Recessive|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes": 1,
    "not_specified|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|not_provided|not_specified": 1,
    "Monogenic_diabetes|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|not_provided|Maturity_onset_diabetes_mellitus_in_young": 2,
    "GCK-related_disorder|not_provided": 2,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|not_provided|Pancytopenia-developmental_delay_syndrome|GCK-related_disorder|Monogenic_diabetes": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes": 1,
    "not_provided|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified": 2,
    "Diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Hyperinsulinism_due_to_glucokinase_deficiency|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|not_provided": 1,
    "Monogenic_diabetes|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|not_specified|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|GCK-related_disorder|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified": 19,
    "Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|Monogenic_diabetes": 4,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Transient_Neonatal_Diabetes|_Recessive|Permanent_neonatal_diabetes_mellitus": 3,
    "Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes|Permanent_neonatal_diabetes_mellitus": 1,
    "GCK-related_disorder|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Gestational_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified": 9,
    "Diabetes_mellitus|not_provided": 1,
    "Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 4,
    "not_specified|not_provided|Monogenic_diabetes": 3,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|GCK-related_disorder|Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified": 8,
    "Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1": 1,
    "Gestational_diabetes": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1": 1,
    "not_specified|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Permanent_neonatal_diabetes_mellitus_1|GCK-related_disorder|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Recessive|not_specified|Hyperinsulinism_due_to_glucokinase_deficiency|not_provided": 2,
    "not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young": 5,
    "GCK-related_disorder|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|GCK-related_disorder|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified": 13,
    "Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1": 1,
    "Transient_Neonatal_Diabetes|_Recessive|not_provided|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_specified|not_provided": 1,
    "not_specified|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Transient_Neonatal_Diabetes|_Recessive|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "Permanent_neonatal_diabetes_mellitus|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "Gestational_diabetes|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|GCK-related_disorder|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1": 1,
    "not_provided|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 1,
    "GCK-related_disorder|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|not_provided|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3": 17,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|GCK-related_disorder|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|GCK-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|not_provided|not_specified": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|not_provided|Gestational_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 15,
    "Monogenic_diabetes|GCK-related_disorder": 1,
    "not_specified|not_provided|GCK-related_disorder|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "not_provided|not_specified|GCK-related_disorder": 1,
    "Transient_Neonatal_Diabetes|_Recessive|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_2|Developmental_and_epileptic_encephalopathy|_2|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_specified|GCK-related_disorder|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "not_specified|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Permanent_neonatal_diabetes_mellitus_1|GCK-related_disorder|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|GCK-related_disorder|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 3,
    "Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Transient_Neonatal_Diabetes|_Recessive|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|not_specified|Permanent_neonatal_diabetes_mellitus|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Transient_Neonatal_Diabetes|_Recessive": 1,
    "not_specified|Transient_Neonatal_Diabetes|_Recessive|Maturity_onset_diabetes_mellitus_in_young|not_provided|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "Permanent_neonatal_diabetes_mellitus_1|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Transient_Neonatal_Diabetes|_Recessive|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Transient_Neonatal_Diabetes|_Recessive|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Permanent_neonatal_diabetes_mellitus|not_specified": 1,
    "Monogenic_diabetes|not_specified": 5,
    "GCK-related_disorder|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive|Hyperinsulinism_due_to_glucokinase_deficiency|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus|not_provided|Transient_Neonatal_Diabetes|_Recessive|not_specified": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1": 1,
    "not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 3,
    "Transient_Neonatal_Diabetes|_Recessive|not_specified|not_provided|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_2|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2": 3,
    "Hyperinsulinism|_Dominant|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes|not_provided": 1,
    "not_provided|not_specified|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "not_specified|Hyperinsulinism_due_to_glucokinase_deficiency|Monogenic_diabetes|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "GCK-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Type_2_diabetes_mellitus|not_provided|not_specified|GCK-related_disorder": 1,
    "Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|not_provided|GCK-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|not_provided|GCK-related_disorder|Monogenic_diabetes": 1,
    "GCK-related_disorder|not_provided|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Monogenic_diabetes": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_2|GCK-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|GCK-related_disorder|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "not_provided|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified|Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Transient_Neonatal_Diabetes|_Recessive": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus": 2,
    "Monogenic_diabetes|not_provided|not_specified": 3,
    "Monogenic_diabetes|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_2|not_provided": 1,
    "Transient_Neonatal_Diabetes|_Recessive|not_provided|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus_1|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinism_due_to_glucokinase_deficiency|Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus_1|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Recessive|Hyperinsulinism_due_to_glucokinase_deficiency|not_provided": 3,
    "Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Recessive|not_specified|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Hyperinsulinism_due_to_glucokinase_deficiency|Transient_Neonatal_Diabetes|_Recessive|not_specified|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism_due_to_glucokinase_deficiency|Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Recessive|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|GCK-related_disorder|Transient_Neonatal_Diabetes|_Recessive|not_specified|Hyperinsulinism_due_to_glucokinase_deficiency": 1,
    "Intellectual_disability|_autosomal_dominant_54": 26,
    "Intellectual_disability|_autosomal_dominant_40|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_54": 8,
    "Inborn_genetic_diseases|CAMK2B-related_disorder|not_provided": 1,
    "CAMK2B-related_disorder|not_provided": 6,
    "not_provided|CAMK2B-related_disorder": 10,
    "CAMK2B-related_disorder": 4,
    "not_provided|Intellectual_disability|_autosomal_dominant_54|CAMK2B-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_54|not_provided": 7,
    "CAMK2B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CAMK2B-related_disorder|Dystonia|_early-onset|_and/or_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_54": 1,
    "Intellectual_disability|_autosomal_dominant_54|CAMK2B-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_54|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_54|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_54|Inborn_genetic_diseases|Intellectual_disability|Agitation|Microcephaly|Apnea|Hyperventilation|Dystonic_disorder|Global_developmental_delay|not_provided|Abnormality_of_the_nervous_system": 1,
    "Intellectual_disability|not_provided|Intellectual_disability|_autosomal_dominant_54": 1,
    "not_provided|Intellectual_disability|Intellectual_disability|_autosomal_dominant_54": 1,
    "NPC1L1-related_disorder": 12,
    "not_specified|Ezetimibe_response|not_provided": 1,
    "LOW_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_7": 2,
    "Statins|_attenuated_cholesterol_lowering_by|not_specified": 1,
    "Ezetimibe_response": 1,
    "not_provided|Oxoglutaricaciduria": 3,
    "Oxoglutaricaciduria": 116,
    "not_provided|OGDH-related_disorder|Oxoglutaricaciduria": 1,
    "not_specified|Oxoglutaricaciduria": 5,
    "not_specified|Oxoglutaricaciduria|OGDH-related_disorder|not_provided": 1,
    "OGDH-related_disorder": 5,
    "not_provided|Oxoglutaricaciduria|OGDH-related_disorder": 3,
    "OGDH-related_disorder|Oxoglutaricaciduria": 4,
    "Oxoglutaricaciduria|OGDH-related_disorder": 3,
    "Oxoglutaricaciduria|OGDH-related_disorder|not_provided": 3,
    "Oxoglutaricaciduria|not_provided": 3,
    "Oxoglutaricaciduria|not_specified": 1,
    "not_provided|Oxoglutaricaciduria|not_specified": 1,
    "not_specified|OGDH-related_disorder|Oxoglutaricaciduria": 1,
    "Oxoglutaricaciduria|not_provided|OGDH-related_disorder": 2,
    "Oxoglutaricaciduria|not_specified|not_provided": 1,
    "Death_in_infancy": 1,
    "Cerebral_cavernous_malformation_2": 145,
    "Cerebral_cavernous_malformation_2|not_provided": 8,
    "not_provided|Cerebral_cavernous_malformation_2": 17,
    "CCM2-related_disorder|not_provided|Cerebral_cavernous_malformation_2": 1,
    "CCM2-related_disorder": 9,
    "not_provided|Cerebral_cavernous_malformation_2|CCM2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Cerebral_cavernous_malformation_2": 1,
    "Cerebral_cavernous_malformation_2|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Cerebral_cavernous_malformation_2": 6,
    "Cerebral_cavernous_angioma|Subcutaneous_venous_lacunae": 1,
    "Inborn_genetic_diseases|CCM2-related_disorder|Cerebral_cavernous_malformation_2": 1,
    "not_provided|Cerebral_cavernous_malformation_2|Inborn_genetic_diseases|not_specified": 1,
    "CCM2-related_disorder|Inborn_genetic_diseases": 1,
    "Vascular_dementia|Cerebral_cavernous_malformation_2": 1,
    "Cerebral_cavernous_malformation_2|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Cerebral_cavernous_malformation_2": 2,
    "Cavernous_hemangioma": 2,
    "Cerebral_cavernous_malformation_2|not_specified|not_provided|CCM2-related_disorder": 2,
    "Cerebral_cavernous_malformation_2|not_specified": 4,
    "Cerebral_cavernous_malformation_2|Inborn_genetic_diseases": 8,
    "Cerebral_cavernous_malformation_2|CCM2-related_disorder|Inborn_genetic_diseases": 2,
    "Cerebral_cavernous_malformation_2|Cerebral_cavernous_malformation": 1,
    "Cerebral_cavernous_malformation_2|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Cerebral_cavernous_malformation_2|Inborn_genetic_diseases": 2,
    "CCM2-related_disorder|Cerebral_cavernous_malformation_2": 3,
    "CCM2-related_disorder|not_specified|not_provided|Cerebral_cavernous_malformation_2": 1,
    "Inborn_genetic_diseases|CCM2-related_disorder": 1,
    "Cerebral_cavernous_malformation_2|CCM2-related_disorder": 1,
    "Cerebral_cavernous_malformation_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Cerebral_cavernous_malformation_2|not_provided": 1,
    "Cerebral_cavernous_malformation_2|Vasculitis": 1,
    "CCM2-related_disorder|not_provided": 1,
    "ADCY1-related_disorder|not_provided": 2,
    "ADCY1-related_disorder": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_44": 4,
    "not_provided|ADCY1-related_disorder": 7,
    "not_provided|ADCY1-related_disorder|not_specified": 1,
    "ADCY1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_44|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_44": 1,
    "ADCY1-related_disorder|not_provided|not_specified": 1,
    "ADCY1-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|ADCY1-related_disorder": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_44|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_44": 1,
    "PKD1L1-related_disorder": 141,
    "PKD1L1-related_disorder|not_provided": 44,
    "Heterotaxy|_visceral|_8|_autosomal": 35,
    "PKD1L1-related_disorder|Inborn_genetic_diseases": 9,
    "PKD1L1-related_disorder|Heterotaxy|_visceral|_8|_autosomal": 1,
    "not_provided|PKD1L1-related_disorder": 40,
    "Inborn_genetic_diseases|PKD1L1-related_disorder": 18,
    "Inborn_genetic_diseases|Heterotaxy|_visceral|_8|_autosomal": 1,
    "not_provided|Heterotaxy|_visceral|_8|_autosomal": 19,
    "Heterotaxy|_visceral|_8|_autosomal|Inborn_genetic_diseases": 4,
    "PKD1L1-related_disorder|Inborn_genetic_diseases|not_provided": 9,
    "Situs_inversus": 29,
    "PKD1L1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Heterotaxy|_visceral|_8|_autosomal|PKD1L1-related_disorder|not_specified": 1,
    "Heterotaxy|_visceral|_8|_autosomal|not_provided": 13,
    "not_provided|Inborn_genetic_diseases|Heterotaxy|_visceral|_8|_autosomal": 1,
    "Congenital_chylothorax": 2,
    "Heterotaxy|_visceral|_8|_autosomal|PKD1L1-related_disorder|Inborn_genetic_diseases|Situs_inversus": 1,
    "PKD1L1-related_disorder|Heterotaxy|_visceral|_8|_autosomal|not_provided": 2,
    "not_provided|PKD1L1-related_disorder|Inborn_genetic_diseases": 2,
    "Heterotaxy|_visceral|_8|_autosomal|Inborn_genetic_diseases|Situs_inversus": 1,
    "PKD1L1-related_disorder|not_provided|not_specified": 1,
    "Heterotaxy|_visceral|_8|_autosomal|PKD1L1-related_disorder": 2,
    "PKD1L1-related_disorder|Congenital_chylothorax|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Heterotaxy|_visceral|_8|_autosomal|PKD1L1-related_disorder": 3,
    "PKD1L1-related_disorder|not_provided|Heterotaxy|_visceral|_8|_autosomal": 3,
    "Heterotaxy|_visceral|_8|_autosomal|not_provided|PKD1L1-related_disorder": 2,
    "Inborn_genetic_diseases|PKD1L1-related_disorder|not_provided": 2,
    "PKD1L1-related_disorder|not_specified|not_provided": 1,
    "PKD1L1-related_disorder|not_specified|Heterotaxy|_visceral|_8|_autosomal|not_provided": 1,
    "Heterotaxy|_visceral|_8|_autosomal|Inborn_genetic_diseases|PKD1L1-related_disorder|not_provided": 1,
    "Heterotaxy|_visceral|_8|_autosomal|Inborn_genetic_diseases|not_provided": 1,
    "Visceral_heterotaxy|Heterotaxy|_visceral|_8|_autosomal": 1,
    "ABCA13-related_disorder": 9,
    "ABCA13-related_disorder|not_specified": 2,
    "not_provided|ABCA13-related_disorder": 5,
    "Intellectual_disability_without_epilepsy": 2,
    "not_provided|ABCA13-related_neurodevelopmental_condition|ABCA13-related_disorder": 1,
    "not_specified|ABCA13-related_disorder": 2,
    "not_specified|ABCA13-related_neurodevelopmental_condition": 1,
    "ABCA13-related_disorder|not_provided": 1,
    "not_specified|ABCA13-related_disorder|not_provided": 1,
    "ZPBP-related_disorder": 12,
    "Spermatogenic_failure_66": 4,
    "not_provided|not_specified|ZPBP-related_disorder": 1,
    "Pancytopenia_due_to_IKZF1_mutations": 15,
    "Acute_lymphoid_leukemia|not_provided": 3,
    "not_provided|Pancytopenia_due_to_IKZF1_mutations": 7,
    "not_provided|IKZF1-related_disorder": 5,
    "IKZF1-related_disorder": 10,
    "not_provided|not_specified|Pancytopenia_due_to_IKZF1_mutations": 1,
    "Acute_lymphoid_leukemia": 39,
    "IKZF1-related_disorder|not_provided|Pancytopenia_due_to_IKZF1_mutations": 1,
    "not_provided|IKZF1-related_disorder|Pancytopenia_due_to_IKZF1_mutations": 1,
    "not_provided|not_specified|IKZF1-related_disorder": 1,
    "IKZF1-related_disorder|not_provided|Acute_lymphoid_leukemia": 1,
    "Pancytopenia_due_to_IKZF1_mutations|not_provided|not_specified": 1,
    "IKZF1-related_disorder|Inherited_Immunodeficiency_Diseases|Pancytopenia_due_to_IKZF1_mutations|Immunodeficiency|not_provided": 1,
    "Pancytopenia_due_to_IKZF1_mutations|not_provided": 4,
    "Inherited_Immunodeficiency_Diseases|Pancytopenia_due_to_IKZF1_mutations|not_provided": 1,
    "Acute_lymphoid_leukemia|Pancytopenia_due_to_IKZF1_mutations": 1,
    "IKZF1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Pancytopenia_due_to_IKZF1_mutations": 1,
    "not_provided|Pancytopenia_due_to_IKZF1_mutations|IKZF1-related_disorder": 1,
    "Leukemia|_acute_lymphocytic|_susceptibility_to|_2": 2,
    "not_specified|Pancytopenia_due_to_IKZF1_mutations|not_provided": 1,
    "Pancytopenia_due_to_IKZF1_mutations|Acute_lymphoid_leukemia|not_provided": 1,
    "IKZF1-related_disorder|not_provided": 2,
    "not_provided|Diamond-Blackfan_anemia-like": 1,
    "not_provided|IKZF1-related_disorder|not_specified": 1,
    "Chronic_myelogenous_leukemia|_BCR-ABL1_positive": 6,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|not_provided": 9,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase": 453,
    "Global_developmental_delay|Inborn_genetic_diseases|Deficiency_of_aromatic-L-amino-acid_decarboxylase|DDC-related_disorder": 1,
    "DDC-related_disorder|not_specified|not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 2,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 3,
    "RASopathy|Deficiency_of_aromatic-L-amino-acid_decarboxylase|not_provided": 1,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|not_specified": 4,
    "Inborn_genetic_diseases|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 6,
    "not_specified|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 1,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|DDC-related_disorder": 2,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|See_cases": 1,
    "DDC-related_disorder|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 8,
    "not_specified|not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 5,
    "not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase|See_cases": 1,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|not_specified|not_provided": 3,
    "not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 8,
    "not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase|DDC-related_disorder": 1,
    "DDC-related_disorder|not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 1,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Deficiency_of_aromatic-L-amino-acid_decarboxylase|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase": 1,
    "Deficiency_of_aromatic-L-amino-acid_decarboxylase|DDC-related_disorder|not_provided": 1,
    "not_provided|Deficiency_of_aromatic-L-amino-acid_decarboxylase|not_specified": 1,
    "GRB10-related_disorder": 13,
    "GRB10-related_disorder|not_provided": 2,
    "not_provided|GRB10-related_disorder": 2,
    "not_provided|Lung_cancer": 2,
    "Lung_carcinoma": 8,
    "EGFR-related_lung_cancer": 1761,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 383,
    "Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 4,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 435,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|EGFR-related_lung_cancer": 15,
    "not_provided|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 6,
    "EGFR-related_lung_cancer|not_provided": 10,
    "EGFR-related_lung_cancer|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Lung_carcinoma": 4,
    "EGFR-related_lung_cancer|not_provided|EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 7,
    "Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_lung_cancer": 3,
    "EGFR-related_lung_cancer|Lung_carcinoma": 2,
    "EGFR-related_lung_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|not_specified": 1,
    "not_provided|See_cases|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "not_provided|EGFR-related_lung_cancer": 8,
    "Hereditary_breast_ovarian_cancer_syndrome|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder": 1,
    "EGFR-related_lung_cancer|EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome": 7,
    "EGFR-related_lung_cancer|EGFR-related_disorder": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer": 6,
    "EGFR-related_disorder|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|EGFR-related_disorder": 9,
    "EGFR-related_lung_cancer|not_provided|not_specified|Lung_cancer|Hereditary_cancer-predisposing_syndrome|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 1,
    "EGFR-related_disorder|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|not_specified": 1,
    "Lung_carcinoma|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|not_provided": 5,
    "Lung_cancer|not_provided|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "EGFR-related_lung_cancer|not_specified|not_provided|Lung_cancer": 1,
    "EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 2,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder": 1,
    "EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer": 3,
    "EGFR-related_lung_cancer|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder|EGFR-related_lung_cancer": 2,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "EGFR-related_disorder|not_provided|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|EGFR-related_disorder|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 3,
    "not_provided|EGFR-related_disorder|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 2,
    "EGFR-related_lung_cancer|Cerebral_palsy": 1,
    "Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2": 2,
    "EGFR-related_lung_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Lung_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 3,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "EGFR-related_disorder": 9,
    "EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 1,
    "EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|EGFR-related_lung_cancer|Lung_cancer": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 2,
    "Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "not_specified|EGFR-related_lung_cancer": 5,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|EGFR-related_lung_cancer": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|EGFR-related_lung_cancer|not_provided": 1,
    "not_provided|Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|EGFR-related_disorder": 1,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "EGFR-related_lung_cancer|EGFR-related_disorder|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lung_cancer|EGFR-related_lung_cancer|not_provided|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Cholangiocarcinoma": 1,
    "not_provided|Ovarian_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "EGFR-related_lung_cancer|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|Lung_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 1,
    "Ovarian_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Lung_carcinoma|EGFR-related_lung_cancer": 1,
    "Lung_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|not_provided|EGFR-related_lung_cancer|Lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cerebral_arteriovenous_malformation": 1,
    "EGFR-related_disorder|not_provided": 1,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2": 1,
    "Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|not_specified": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 3,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Lung_carcinoma": 1,
    "EGFR-related_lung_cancer|not_provided|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_lung_cancer": 1,
    "EGFR-related_disorder|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|EGFR-related_lung_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|EGFR-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|not_specified": 1,
    "not_specified|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "EGFR-related_lung_cancer|Lung_cancer": 31,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|EGFR-related_lung_cancer": 11,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 5,
    "Lung_cancer|EGFR-related_lung_cancer": 11,
    "Tyrosine_kinase_inhibitor_response": 39,
    "not_specified|Lung_adenocarcinoma|Lung_carcinoma": 2,
    "Lung_carcinoma|Tyrosine_kinase_inhibitor_response": 1,
    "EGFR-related_lung_cancer|Lung_cancer|Hereditary_cancer-predisposing_syndrome": 8,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Lung_cancer": 9,
    "Nonsmall_cell_lung_cancer|_response_to_tyrosine_kinase_inhibitor_in|_somatic|EGFR-related_lung_cancer|Tyrosine_kinase_inhibitor_response|Lung_adenocarcinoma": 1,
    "Non-small_cell_lung_carcinoma|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Non-small_cell_lung_carcinoma|Nonsmall_cell_lung_cancer|_response_to_tyrosine_kinase_inhibitor_in|_somatic": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Lung_cancer|EGFR-related_lung_cancer": 2,
    "not_provided|EGFR-related_lung_cancer|Lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|not_provided|EGFR-related_lung_cancer|not_specified": 1,
    "Lung_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Lung_cancer|EGFR-related_disorder": 1,
    "Lung_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 9,
    "Squamous_cell_carcinoma_of_the_head_and_neck": 18,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|EGFR-related_lung_cancer": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|EGFR-related_lung_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Lung_cancer": 7,
    "EGFR-related_lung_cancer|not_specified|Lung_cancer": 1,
    "Tyrosine_kinase_inhibitor_response|Lung_adenocarcinoma|EGFR-related_lung_cancer": 1,
    "not_provided|Lung_adenocarcinoma|Tyrosine_kinase_inhibitor_response": 1,
    "Lung_adenocarcinoma|Tyrosine_kinase_inhibitor_response": 4,
    "Tyrosine_kinase_inhibitor_response|Lung_adenocarcinoma": 1,
    "Nonsmall_cell_lung_cancer|_response_to_tyrosine_kinase_inhibitor_in|_somatic|Tyrosine_kinase_inhibitor_response": 1,
    "Nonsmall_cell_lung_cancer|_response_to_tyrosine_kinase_inhibitor_in|_somatic|Lung_adenocarcinoma|Tyrosine_kinase_inhibitor_response": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder|EGFR-related_lung_cancer|not_provided": 1,
    "Lung_cancer|not_provided": 1,
    "EGFR-related_lung_cancer|Lung_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 3,
    "EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome|Lung_cancer|not_specified|EGFR-related_lung_cancer|not_provided": 1,
    "Non-small_cell_lung_carcinoma|Tyrosine_kinase_inhibitor_response|Lung_adenocarcinoma": 1,
    "not_provided|Lung_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_carcinoma|EGFR-related_lung_cancer|Lung_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Lung_adenocarcinoma": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|Lung_cancer|not_specified": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|EGFR-related_lung_cancer": 2,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|not_provided|not_specified|Lung_carcinoma|Lung_cancer|Squamous_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "EGFR-related_disorder|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Hereditary_cancer-predisposing_syndrome|not_provided|EGFR-related_lung_cancer|Non-small_cell_lung_carcinoma|Lung_adenocarcinoma|Tyrosine_kinase_inhibitor_response|gefitinib_response_-_Efficacy|erlotinib_response_-_Efficacy": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|EGFR-related_lung_cancer": 1,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|EGFR-related_lung_cancer|EGFR-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|not_specified|EGFR-related_lung_cancer|not_provided": 1,
    "not_provided|not_specified|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Lung_carcinoma|EGFR-related_lung_cancer|Lung_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lung_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|not_specified|not_provided|EGFR-related_lung_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|not_provided|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|Squamous_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome|Lung_adenocarcinoma|not_specified": 1,
    "not_specified|Lung_adenocarcinoma": 1,
    "Non-small_cell_lung_carcinoma|Lung_adenocarcinoma": 5,
    "EGFR-related_lung_cancer|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Lung_cancer": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lung_cancer|EGFR-related_lung_cancer": 1,
    "not_provided|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "EGFR-related_lung_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Lung_cancer|Lung_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|EGFR-related_lung_cancer|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer": 1,
    "gefitinib_response_-_Efficacy|Hereditary_cancer-predisposing_syndrome|Lung_adenocarcinoma|Tyrosine_kinase_inhibitor_response|Nonsmall_cell_lung_cancer|_response_to_tyrosine_kinase_inhibitor_in|_somatic|Adenocarcinoma_of_lung|_response_to_tyrosine_kinase_inhibitor_in|_somatic|Lung_carcinoma": 1,
    "Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|not_provided|EGFR-related_lung_cancer": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_lung_cancer|not_provided": 1,
    "not_provided|EGFR-related_lung_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "EGFR-related_disorder|EGFR-related_lung_cancer": 4,
    "Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|EGFR-related_lung_cancer|not_provided": 1,
    "Hereditary_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Lung_carcinoma|Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|not_specified": 1,
    "EGFR-related_lung_cancer|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|EGFR-related_disorder|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|not_provided|Lung_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_lung_cancer|EGFR-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Diffuse_midline_glioma|_H3_K27-altered|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|Lung_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "EGFR-related_disorder|not_specified": 1,
    "EGFR-related_disorder|Lung_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Lung_cancer|not_provided|EGFR-related_lung_cancer": 1,
    "EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|EGFR-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|EGFR-related_lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|EGFR-related_lung_cancer": 1,
    "not_provided|EGFR-related_lung_cancer|Lung_cancer|Inflammatory_skin_and_bowel_disease|_neonatal|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Inflammatory_skin_and_bowel_disease|_neonatal|_2|Lung_cancer|Hereditary_cancer|EGFR-related_lung_cancer|Hereditary_cancer-predisposing_syndrome|Diffuse_midline_glioma|_H3_K27-altered|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 3,
    "Deficiency_of_phosphoserine_phosphatase": 122,
    "Deficiency_of_phosphoserine_phosphatase|not_provided": 16,
    "Deficiency_of_phosphoserine_phosphatase|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Deficiency_of_phosphoserine_phosphatase": 6,
    "Deficiency_of_phosphoserine_phosphatase|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Deficiency_of_phosphoserine_phosphatase": 3,
    "not_provided|PSPH-related_disorder|Deficiency_of_phosphoserine_phosphatase": 1,
    "Amelogenesis_imperfecta|Deficiency_of_phosphoserine_phosphatase": 1,
    "PSPH-related_disorder": 2,
    "not_provided|Neurometabolic_disorder_due_to_serine_deficiency|not_specified": 1,
    "not_provided|Deficiency_of_phosphoserine_phosphatase|not_specified": 1,
    "not_specified|Deficiency_of_phosphoserine_phosphatase|not_provided": 1,
    "Deficiency_of_phosphoserine_phosphatase|not_provided|not_specified": 1,
    "Deficiency_of_phosphoserine_phosphatase|PSPH-related_disorder|not_provided": 1,
    "Deficiency_of_phosphoserine_phosphatase|not_specified|not_provided": 1,
    "SUMF2-related_disorder": 6,
    "not_specified|SUMF2-related_disorder": 1,
    "SUMF2-related_disorder|not_provided": 1,
    "not_provided|CHCHD2-related_disorder": 2,
    "not_provided|Parkinson_disease_22|_autosomal_dominant": 2,
    "CHCHD2-related_disorder": 1,
    "Parkinson_disease_22|_autosomal_dominant": 2,
    "Parkinson_disease_22|_autosomal_dominant|not_provided": 1,
    "CHCHD2-related_disorder|not_provided": 1,
    "Mucopolysaccharidosis_type_7": 540,
    "Mucopolysaccharidosis_type_7|not_provided": 14,
    "not_specified|not_provided|Mucopolysaccharidosis_type_7": 1,
    "Mucopolysaccharidosis_type_7|GUSB-related_disorder": 8,
    "GUSB-related_disorder|Mucopolysaccharidosis_type_7": 5,
    "GUSB-related_disorder|not_provided": 1,
    "GUSB-related_disorder|Mucopolysaccharidosis_type_7|not_provided": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis_type_7": 13,
    "not_specified|Mucopolysaccharidosis_type_7": 6,
    "not_provided|not_specified|Mucopolysaccharidosis_type_7": 2,
    "not_provided|Mucopolysaccharidosis_type_7|not_specified": 2,
    "not_specified|Mucopolysaccharidosis_type_7|not_provided": 3,
    "not_provided|Mucopolysaccharidosis_type_7": 14,
    "not_specified|Non-immune_hydrops_fetalis": 1,
    "not_provided|Mucopolysaccharidosis_type_7|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis_type_7|not_specified": 2,
    "Mucopolysaccharidosis_type_6|Mucopolysaccharidosis_type_7": 1,
    "Mucopolysaccharidosis_type_7|Inborn_genetic_diseases": 6,
    "Non-immune_hydrops_fetalis|Mucopolysaccharidosis_type_7": 2,
    "not_provided|GUSB-related_disorder": 1,
    "not_provided|Non-immune_hydrops_fetalis|Mucopolysaccharidosis_type_7": 1,
    "GUSB-related_disorder": 1,
    "Mucopolysaccharidosis_type_7|not_provided|Inborn_genetic_diseases": 1,
    "GUSB-related_disorder|not_provided|Mucopolysaccharidosis_type_6|Mucopolysaccharidosis_type_7": 1,
    "not_provided|Mucopolysaccharidosis_type_7|Intellectual_disability": 1,
    "GUSB-related_disorder|not_provided|Mucopolysaccharidosis_type_7": 1,
    "Mucopolysaccharidosis_type_7|not_specified|not_provided": 1,
    "Argininosuccinate_lyase_deficiency|not_specified": 13,
    "Argininosuccinate_lyase_deficiency": 713,
    "not_specified|Argininosuccinate_lyase_deficiency": 21,
    "Argininosuccinate_lyase_deficiency|Inborn_genetic_diseases": 9,
    "not_provided|Argininosuccinate_lyase_deficiency": 34,
    "Inborn_genetic_diseases|ASL-related_disorder|not_provided|Argininosuccinate_lyase_deficiency": 1,
    "Inborn_genetic_diseases|Argininosuccinate_lyase_deficiency": 6,
    "Argininosuccinate_lyase_deficiency|not_provided": 15,
    "Argininosuccinate_lyase_deficiency|ASL-related_disorder": 2,
    "not_specified|not_provided|Argininosuccinate_lyase_deficiency": 10,
    "Inborn_genetic_diseases|not_specified|Argininosuccinate_lyase_deficiency": 1,
    "ASL-related_disorder": 3,
    "ASL-related_disorder|Argininosuccinate_lyase_deficiency": 2,
    "not_provided|Autism|Argininosuccinate_lyase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Argininosuccinate_lyase_deficiency": 3,
    "not_specified|Argininosuccinate_lyase_deficiency|ASL-related_disorder": 1,
    "not_provided|Argininosuccinate_lyase_deficiency|Inborn_genetic_diseases": 1,
    "Argininosuccinate_lyase_deficiency|not_provided|ASL-related_disorder": 1,
    "Neurodevelopmental_disorder|not_provided|Argininosuccinate_lyase_deficiency": 1,
    "ASL-related_disorder|not_provided|Argininosuccinate_lyase_deficiency": 2,
    "not_specified|Argininosuccinate_lyase_deficiency|not_provided": 1,
    "not_provided|not_specified|Argininosuccinate_lyase_deficiency": 1,
    "Congenital_myasthenic_syndrome_4C": 31,
    "Progressive_myoclonic_epilepsy_type_3": 290,
    "not_provided|Progressive_myoclonic_epilepsy_type_3": 18,
    "Progressive_myoclonic_epilepsy_type_3|not_specified": 4,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy_type_3": 4,
    "Progressive_myoclonic_epilepsy_type_3|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_3": 8,
    "Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy_type_3": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Progressive_myoclonic_epilepsy_type_3": 3,
    "Progressive_myoclonic_epilepsy_type_3|Neuronal_ceroid_lipofuscinosis_1": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_3": 7,
    "not_specified|Progressive_myoclonic_epilepsy_type_3|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_3|not_provided": 23,
    "Progressive_myoclonic_epilepsy_type_3|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_3|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_3|Epilepsy|_progressive_myoclonic|_3|_with_intracellular_inclusions": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Progressive_myoclonic_epilepsy_type_3": 1,
    "Inborn_genetic_diseases|not_specified|Progressive_myoclonic_epilepsy_type_3|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_3|Inborn_genetic_diseases|not_provided": 2,
    "KCTD7-related_disorder|Progressive_myoclonic_epilepsy_type_3": 1,
    "Progressive_myoclonic_epilepsy_type_3|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Progressive_myoclonic_epilepsy_type_3": 1,
    "KCTD7-related_disorder|not_specified|Progressive_myoclonic_epilepsy_type_3": 1,
    "Inborn_genetic_diseases|not_specified|Progressive_myoclonic_epilepsy_type_3|Epileptic_encephalopathy|Intellectual_disability": 1,
    "not_provided|not_specified|KCTD7-related_disorder|Progressive_myoclonic_epilepsy_type_3": 1,
    "not_provided|not_specified|Progressive_myoclonic_epilepsy_type_3": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_3|not_specified": 1,
    "Progressive_myoclonic_epilepsy_type_3|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Epilepsy|_progressive_myoclonic|_3|_with_intracellular_inclusions|Progressive_myoclonic_epilepsy_type_3": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_3|Intellectual_disability|not_provided": 1,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy_type_3|Inborn_genetic_diseases": 1,
    "KCTD7-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Progressive_myoclonic_epilepsy_type_3": 1,
    "KCTD7-related_disorder|not_provided|Progressive_myoclonic_epilepsy_type_3": 1,
    "KCTD7-related_disorder": 2,
    "Progressive_myoclonic_epilepsy_type_3|Intellectual_disability": 1,
    "not_provided|Shwachman-Diamond_syndrome_1": 2,
    "not_provided|Aplastic_anemia|Shwachman-Diamond_syndrome_1|Inborn_genetic_diseases": 1,
    "Shwachman-Diamond_syndrome_1": 23,
    "not_provided|Shwachman-Diamond_syndrome_1|Aplastic_anemia": 1,
    "Shwachman-Diamond_syndrome_1|not_specified|Aplastic_anemia": 1,
    "Aplastic_anemia|Shwachman-Diamond_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Aplastic_anemia|not_specified|Shwachman-Diamond_syndrome_1": 1,
    "not_specified|Inborn_genetic_diseases|Aplastic_anemia|not_provided|Shwachman-Diamond_syndrome_1": 1,
    "Shwachman-Diamond_syndrome_1|Aplastic_anemia": 4,
    "SBDS-related_disorder": 1,
    "Inborn_genetic_diseases|Shwachman-Diamond_syndrome_1": 1,
    "Shwachman-Diamond_syndrome_1|Aplastic_anemia|not_provided": 3,
    "Shwachman-Diamond_syndrome_1|Inborn_genetic_diseases": 1,
    "Aplastic_anemia|Shwachman-Diamond_syndrome_1": 5,
    "Inborn_genetic_diseases|not_provided|Shwachman-Diamond_syndrome_1": 1,
    "Shwachman-Diamond_syndrome_1|not_specified": 1,
    "Aplastic_anemia|Shwachman-Diamond_syndrome_1|SBDS-related_disorder|not_provided": 1,
    "Shwachman-Diamond_syndrome_1|not_provided|Aplastic_anemia|not_specified": 1,
    "SBDS-related_disorder|Shwachman_syndrome|Aplastic_anemia|Shwachman-Diamond_syndrome_1|Inborn_genetic_diseases|not_specified|not_provided|Aplastic_anemia|_susceptibility_to|Microcephaly|Agenesis_of_permanent_teeth|Deeply_set_eye|Short_stature|Splenomegaly|Intellectual_disability": 1,
    "Aplastic_anemia|Shwachman-Diamond_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Aplastic_anemia|Inborn_genetic_diseases|not_specified|Shwachman-Diamond_syndrome_1": 1,
    "Inborn_genetic_diseases|Shwachman-Diamond_syndrome_1|Aplastic_anemia|Short_stature|Splenomegaly|Deeply_set_eye|Agenesis_of_permanent_teeth|Microcephaly|not_provided|Intellectual_disability": 1,
    "SBDS-related_disorder|Aplastic_anemia|Shwachman-Diamond_syndrome_1|Shwachman_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Shwachman-Diamond_syndrome_1|Aplastic_anemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Shwachman-Diamond_syndrome_1": 1,
    "Shwachman-Diamond_syndrome_1|not_provided": 2,
    "Shwachman-Diamond_syndrome_1|Aplastic_anemia|not_specified|not_provided": 1,
    "not_specified|SBDS-related_disorder": 1,
    "Aplastic_anemia|not_provided": 3,
    "SBDS-related_disorder|Inborn_genetic_diseases": 1,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency": 85,
    "AUTS2-related_disorder|Intellectual_disability|not_provided": 2,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided": 15,
    "Inborn_genetic_diseases|AUTS2-related_disorder": 2,
    "AUTS2-related_disorder|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 2,
    "not_provided|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 15,
    "not_provided|AUTS2-related_disorder": 15,
    "Inborn_genetic_diseases|AUTS2-related_disorder|not_provided": 3,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|Intellectual_disability|_autosomal_dominant_57|not_provided": 1,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|AUTS2-related_disorder|not_provided": 1,
    "AUTS2-related_disorder": 26,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|AUTS2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "AUTS2-related_disorder|not_specified|not_provided": 1,
    "AUTS2-related_disorder|not_provided": 15,
    "not_provided|Syndromic_intellectual_disability": 3,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided|AUTS2-related_disorder|concomitant_exotropia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|AUTS2-related_disorder": 1,
    "not_specified|not_provided|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 1,
    "AUTS2-related_disorder|Inborn_genetic_diseases|Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided": 1,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|Intellectual_disability|not_provided": 1,
    "not_provided|Neurodevelopmental_abnormality|Inborn_genetic_diseases|See_cases|AUTS2-related_disorder|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 1,
    "Congenital_cerebellar_hypoplasia|Multiple_congenital_anomalies|Corpus_callosum|_agenesis_of|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 1,
    "Pierre_Robin-like_syndrome": 1,
    "See_cases|Inborn_genetic_diseases|not_provided|AUTS2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 3,
    "Intellectual_disability|AUTS2-related_disorder|not_provided": 1,
    "not_provided|Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|AUTS2-related_disorder": 1,
    "not_provided|Intellectual_disability|AUTS2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|AUTS2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 3,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "AUTS2-related_disorder|Inborn_genetic_diseases": 1,
    "15q11q13_microduplication_syndrome|not_provided": 1,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided|Autism|Global_developmental_delay": 1,
    "Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided|AUTS2-related_disorder": 1,
    "Inborn_genetic_diseases|Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided": 1,
    "AUTS2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Autism_spectrum_disorder_due_to_AUTS2_deficiency": 2,
    "not_provided|AUTS2-related_disorder|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Male_infertility|Spermatogenic_failure_77": 5,
    "FKBP6-related_disorder": 3,
    "BAZ1B-related_disorder": 7,
    "BAZ1B-related_disorder|not_provided": 1,
    "Williams_syndrome": 4,
    "not_provided|BAZ1B-related_disorder": 1,
    "Microcephaly|not_specified": 2,
    "Williams_syndrome|not_provided": 1,
    "not_provided|Williams_syndrome": 1,
    "MLXIPL-related_disorder": 1,
    "Leber-like_hereditary_optic_neuropathy|_autosomal_recessive_1": 7,
    "Leber_hereditary_optic_neuropathy|_autosomal_recessive": 1,
    "Leber_optic_atrophy|_susceptibility_to|Retinal_dystrophy|not_provided|Leber-like_hereditary_optic_neuropathy|_autosomal_recessive_1|Leber_hereditary_optic_neuropathy|_autosomal_recessive|DNAJC30-associated_disorder|Optic_atrophy": 1,
    "DNAJC30-related_disorder": 2,
    "STX1A-related_disorder": 4,
    "Autism|Intellectual_disability": 4,
    "Neurodevelopmental_abnormality|Intellectual_disability|Seizure": 1,
    "Cutis_laxa|_autosomal_dominant|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome": 1,
    "Cutis_laxa|_autosomal_dominant|not_provided|Supravalvar_aortic_stenosis": 3,
    "Supravalvar_aortic_stenosis": 588,
    "not_provided|Supravalvar_aortic_stenosis": 53,
    "Supravalvar_aortic_stenosis|not_specified": 13,
    "Supravalvar_aortic_stenosis|not_provided": 46,
    "Supravalvar_aortic_stenosis|ELN-related_disorder": 9,
    "ELN-related_disorder|Supravalvar_aortic_stenosis": 9,
    "Supravalvar_aortic_stenosis|not_provided|Inborn_genetic_diseases": 4,
    "Supravalvar_aortic_stenosis|not_provided|not_specified": 1,
    "Cutis_laxa|_autosomal_dominant_1|Williams_syndrome|Supravalvar_aortic_stenosis|not_provided": 1,
    "ELN-related_disorder": 24,
    "Inborn_genetic_diseases|Supravalvar_aortic_stenosis": 11,
    "Cutis_laxa|_autosomal_dominant_1|Williams_syndrome|Supravalvar_aortic_stenosis": 1,
    "Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|not_specified": 1,
    "not_specified|not_provided|Supravalvar_aortic_stenosis": 5,
    "Supravalvar_aortic_stenosis|not_specified|not_provided": 5,
    "Williams_syndrome|Supravalvar_aortic_stenosis": 1,
    "not_specified|Supravalvar_aortic_stenosis": 12,
    "Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 24,
    "not_provided|Supravalvar_aortic_stenosis|not_specified": 3,
    "Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis": 21,
    "not_provided|Supravalvar_aortic_stenosis|ELN-related_disorder": 2,
    "Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome": 1,
    "Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "ELN-related_disorder|not_specified|not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 1,
    "not_specified|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|not_provided": 1,
    "ELN-related_disorder|not_provided|Supravalvar_aortic_stenosis": 5,
    "Cutis_laxa|_autosomal_dominant_1|ELN-related_disorder|Supravalvar_aortic_stenosis|Williams_syndrome|not_specified": 1,
    "not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 9,
    "Supravalvar_aortic_stenosis|Inborn_genetic_diseases": 8,
    "Supravalvar_aortic_stenosis|Inborn_genetic_diseases|Cutis_laxa|_autosomal_dominant_1": 1,
    "ELN-related_disorder|not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 2,
    "not_provided|ELN-related_disorder|Supravalvar_aortic_stenosis|Familial_atrioventricular_septal_defect|Cutis_laxa|_autosomal_dominant_1": 1,
    "not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|ELN-related_disorder": 2,
    "not_provided|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis": 6,
    "ELN-related_disorder|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome": 1,
    "Supravalvar_aortic_stenosis|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome": 1,
    "ELN-related_disorder|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 1,
    "not_provided|Supravalvar_aortic_stenosis|not_specified|Cutis_laxa|_autosomal_dominant": 1,
    "not_specified|ELN-related_disorder|Supravalvar_aortic_stenosis": 1,
    "not_provided|ELN-related_disorder|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 2,
    "Supravalvar_aortic_stenosis|not_provided|Cutis_laxa|_autosomal_dominant_1": 5,
    "Cutis_laxa|_autosomal_dominant_1|not_provided|Supravalvar_aortic_stenosis": 1,
    "Inborn_genetic_diseases|not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 2,
    "Inborn_genetic_diseases|ELN-related_disorder": 1,
    "Supravalvar_aortic_stenosis|not_provided|ELN-related_disorder": 4,
    "not_provided|not_specified|Supravalvar_aortic_stenosis": 2,
    "Cutis_laxa|_autosomal_dominant_1|not_specified|Supravalvar_aortic_stenosis": 1,
    "Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|Williams_syndrome|not_provided": 2,
    "Supravalvar_aortic_stenosis|not_provided|Vascular_dilatation|Ascending_tubular_aorta_aneurysm": 1,
    "Inborn_genetic_diseases|not_provided|Supravalvar_aortic_stenosis": 3,
    "ELN-related_disorder|Cutis_laxa|_autosomal_dominant_1|not_provided|Supravalvar_aortic_stenosis": 3,
    "Inborn_genetic_diseases|Supravalvar_aortic_stenosis|Varicose_disease|Colorectal_polyposis|Bruising_susceptibility|Inguinal_hernia|Prominent_superficial_blood_vessels|Dilatation_of_the_sinus_of_Valsalva|Aortic_root_aneurysm|Gastrointestinal_carcinoma|not_provided": 1,
    "ELN-related_disorder|Cutis_laxa|_autosomal_dominant|not_provided|not_specified|Supravalvar_aortic_stenosis": 1,
    "Supravalvar_aortic_stenosis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant|Supravalvar_aortic_stenosis|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant|Supravalvar_aortic_stenosis": 1,
    "Cutis_laxa|_autosomal_dominant|Supravalvar_aortic_stenosis|not_specified": 1,
    "Supravalvar_aortic_stenosis|Williams_syndrome|Cutis_laxa|_autosomal_dominant_1": 1,
    "Hypertelorism|Venous_malformation|Dural_ectasia|Abnormal_digit_morphology|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|not_specified|not_provided": 1,
    "not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant|Williams_syndrome": 1,
    "Inborn_genetic_diseases|Supravalvar_aortic_stenosis|not_provided": 2,
    "Supravalvar_aortic_stenosis|not_specified|Cutis_laxa|_autosomal_dominant|not_provided": 1,
    "not_provided|ELN-related_disorder|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|not_specified": 1,
    "not_specified|not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1": 1,
    "not_provided|Supravalvar_aortic_stenosis|Inborn_genetic_diseases": 2,
    "not_provided|Supravalvar_aortic_stenosis|See_cases|Inborn_genetic_diseases": 1,
    "not_provided|Supravalvar_aortic_stenosis|not_specified|Cutis_laxa|_autosomal_dominant_1": 1,
    "Cutis_laxa|_autosomal_dominant_1": 6,
    "ELN-related_disorder|not_specified|not_provided|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis": 1,
    "ELN-related_disorder|not_provided|See_cases|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome": 1,
    "Supravalvar_aortic_stenosis|See_cases": 1,
    "Williams_syndrome|Supravalvar_aortic_stenosis|not_provided": 1,
    "Inborn_genetic_diseases|Williams_syndrome|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|not_provided|ELN-related_disorder": 1,
    "Supravalvar_aortic_stenosis|not_specified|Cutis_laxa|_autosomal_dominant_1|not_provided": 1,
    "Thoracic_aortic_aneurysm_or_dissection": 8,
    "Cutis_laxa|_autosomal_dominant_1|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|not_provided": 1,
    "not_provided|Cutis_laxa|_autosomal_dominant_1|not_specified|Supravalvar_aortic_stenosis": 1,
    "Cutis_laxa|_autosomal_dominant_1|Inborn_genetic_diseases|Supravalvar_aortic_stenosis|not_provided": 1,
    "Inborn_genetic_diseases|Supravalvar_aortic_stenosis|Williams_syndrome|Cutis_laxa|_autosomal_dominant_1|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant|ELN-related_disorder|not_specified|not_provided|Supravalvar_aortic_stenosis": 1,
    "Supravalvar_aortic_stenosis|not_specified|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome": 1,
    "not_provided|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|not_specified": 1,
    "Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant_1|not_provided|ELN-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Supravalvar_aortic_stenosis": 1,
    "not_specified|not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant": 1,
    "Supravalvar_aortic_stenosis|ELN-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Supravalvar_aortic_stenosis|ELN-related_disorder|Cutis_laxa|_autosomal_dominant_1|Williams_syndrome|not_provided|not_specified": 1,
    "not_specified|Cutis_laxa|_autosomal_dominant_1|not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis": 1,
    "Supravalvar_aortic_stenosis|not_specified|not_provided|Cutis_laxa|_autosomal_dominant_1": 1,
    "Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|Williams_syndrome|not_provided|ELN-related_disorder": 1,
    "Cutis_laxa|_autosomal_dominant_1|Supravalvar_aortic_stenosis|Williams_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Supravalvar_aortic_stenosis|not_provided": 1,
    "not_provided|Supravalvar_aortic_stenosis|ELN-related_disorder|not_specified": 1,
    "ELN-related_disorder|not_provided": 1,
    "Supravalvar_aortic_stenosis|Inborn_genetic_diseases|not_provided|Cutis_laxa|_autosomal_dominant_1": 1,
    "Cutis_laxa|_autosomal_dominant_1|Williams_syndrome|Supravalvar_aortic_stenosis|not_provided|not_specified|Cutis_laxa|_autosomal_dominant": 1,
    "Cutis_laxa|_autosomal_dominant|not_provided|Supravalvar_aortic_stenosis|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Supravalvar_aortic_stenosis|not_specified": 1,
    "Cutis_laxa|_autosomal_dominant|not_specified|not_provided|Supravalvar_aortic_stenosis": 1,
    "Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant": 4,
    "Supravalvar_aortic_stenosis|not_provided|Cutis_laxa|_autosomal_dominant": 1,
    "not_provided|Supravalvar_aortic_stenosis|Cutis_laxa|_autosomal_dominant": 1,
    "not_provided|LIMK1-related_disorder": 6,
    "LIMK1-related_disorder|not_provided": 1,
    "LIMK1-related_disorder": 6,
    "Undetermined_early-onset_epileptic_encephalopathy": 3,
    "not_specified|LIMK1-related_disorder|not_provided": 1,
    "not_provided|GTF2IRD1-related_disorder": 10,
    "GTF2IRD1-related_disorder": 11,
    "GTF2IRD1-related_disorder|not_provided": 6,
    "GTF2IRD1-related_disorder|not_specified|not_provided": 1,
    "GTF2I_related_condition": 1,
    "not_provided|Granulomatous_disease|_chronic|_X-linked|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_1": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_1": 9,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_1": 4,
    "Granulomatous_disease|_chronic|_X-linked|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_1|not_provided": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_1|Chronic_granulomatous_disease|not_provided": 1,
    "HIP1-related_disorder": 11,
    "not_provided|HIP1-related_disorder": 5,
    "not_specified|not_provided|HIP1-related_disorder": 1,
    "HIP1-related_disorder|not_provided": 5,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 577,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 32,
    "not_provided|POR-related_disorder|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "POR-related_disorder": 3,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|not_provided": 3,
    "Inborn_genetic_diseases|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 12,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 5,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Inborn_genetic_diseases": 7,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 14,
    "not_specified|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 13,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided": 22,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Inborn_genetic_diseases": 2,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|not_provided": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|POR-related_disorder": 8,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|POR-related_disorder": 1,
    "Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "not_specified|not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 3,
    "not_provided|not_specified|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|POR-related_disorder|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 2,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 9,
    "Inborn_genetic_diseases|POR-related_disorder": 1,
    "POR-related_disorder|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 10,
    "not_specified|not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "POR-related_disorder|not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|not_specified": 1,
    "not_provided|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified": 1,
    "not_specified|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "POR-related_disorder|not_provided|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Congenital_adrenal_hyperplasia|not_provided|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided|POR-related_disorder|Inborn_genetic_diseases": 1,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Disorder_of_sexual_differentiation|not_provided": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided|not_specified": 2,
    "POR-related_disorder|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided": 1,
    "not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_specified|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "not_specified|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided": 2,
    "Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|not_provided": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified|not_provided": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|not_specified|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_provided|not_specified|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "not_specified|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified": 3,
    "not_provided|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|not_provided": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified|POR-related_disorder": 1,
    "POR-related_disorder|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided|not_specified": 1,
    "not_specified|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "not_specified|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "not_specified|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "POR-related_disorder|Congenital_adrenal_hyperplasia|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "Congenital_adrenal_hyperplasia|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "Congenital_adrenal_hyperplasia|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Congenital_adrenal_hyperplasia": 1,
    "Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_specified|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided|POR-related_disorder": 1,
    "not_provided|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Congenital_adrenal_hyperplasia|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis": 1,
    "Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|not_provided": 1,
    "Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency|Congenital_adrenal_hyperplasia|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis": 1,
    "POR-related_disorder|not_provided|Antley-Bixler_syndrome_with_genital_anomalies_and_disordered_steroidogenesis|Congenital_adrenal_hyperplasia_due_to_cytochrome_P450_oxidoreductase_deficiency": 1,
    "Ambiguous_genitalia": 1,
    "STYXL1-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_51": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy|_51": 4,
    "Developmental_and_epileptic_encephalopathy|_51|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_51|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_51|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_51|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Developmental_and_epileptic_encephalopathy|_51|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_51|Inborn_genetic_diseases": 2,
    "not_provided|Infantile_encephalopathy|Developmental_and_epileptic_encephalopathy|_51": 1,
    "not_provided|MDH2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "MDH2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_51": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_51": 1,
    "MDH2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_51|Infantile_encephalopathy": 1,
    "Infantile_encephalopathy|Developmental_and_epileptic_encephalopathy|_51": 1,
    "MDH2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_51|not_provided|MDH2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_51": 2,
    "Inborn_genetic_diseases|not_provided|MDH2-related_disorder": 2,
    "MDH2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_51|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_51": 1,
    "MDH2-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 8,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided|Neuronopathy|_distal_hereditary_motor|_type_2B": 2,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 3,
    "not_provided|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F": 186,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2F": 7,
    "HSPB1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F": 16,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|not_specified|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F": 8,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|HSPB1-related_disorder|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|not_specified": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases": 8,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|HSPB1-related_disorder|Charcot-Marie-Tooth_disease|HSPB1-related_axonal_neuropathies": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease": 2,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F": 2,
    "Neuronopathy|_distal_hereditary_motor|_type_2B|not_provided": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_C|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B|HSPB1-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "not_provided|HSPB1-related_disorder": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases|not_provided": 1,
    "HSPB1-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "Inborn_genetic_diseases|Distal_hereditary_motor_neuropathy_type_2|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "HSPB1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 1,
    "Inborn_genetic_diseases|HSPB1-related_disorder": 1,
    "not_provided|HSPB1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|not_specified|Hereditary_peripheral_neuropathy": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided|Inborn_genetic_diseases": 2,
    "HSPB1-related_axonal_neuropathies|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F": 2,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2F|Neuronopathy|_distal_hereditary_motor|_type_2B": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2F|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2B|Charcot-Marie-Tooth_disease_axonal_type_2F": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_type_2": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_56": 3,
    "Developmental_and_epileptic_encephalopathy|_56": 13,
    "YWHAG-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_56|not_provided": 3,
    "YWHAG-related_disorder": 2,
    "YWHAG-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_56|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_56|Inborn_genetic_diseases|not_provided": 1,
    "Constipation|Spasticity|Seizure|Failure_to_thrive|Severe_global_developmental_delay|Microcephaly|Intellectual_disability|Hypotonia|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_56|YWHAG-related_disorder|not_provided": 1,
    "Bilateral_tonic-clonic_seizure|Specific_learning_disability": 1,
    "not_specified|ZP3-related_disorder": 1,
    "ZP3-related_disorder": 3,
    "Oocyte_maturation_defect_3": 5,
    "Oocyte_maturation_defect_3|Empty_follicle_syndrome": 1,
    "Empty_ovarian_follicle": 1,
    "not_specified|Oocyte_maturation_defect_3": 1,
    "Oocyte_maturation_defect_3|not_provided": 1,
    "Male_infertility_with_spermatogenesis_disorder_due_to_single_gene_mutation": 1,
    "Male_infertility_due_to_sperm_motility_disorder|Spermatogenic_failure_94": 1,
    "Male_infertility_with_spermatogenesis_disorder_due_to_single_gene_mutation|Male_infertility_due_to_sperm_motility_disorder|Spermatogenic_failure_94": 1,
    "PTPN12-related_disorder": 8,
    "not_provided|PTPN12-related_disorder": 2,
    "PTPN12-related_disorder|not_specified": 1,
    "Nephrotic_syndrome_15|not_specified": 12,
    "not_provided|not_specified|Nephrotic_syndrome_15|MAGI2-related_disorder": 1,
    "Nephrotic_syndrome_15": 134,
    "Nephrotic_syndrome_15|not_provided|not_specified": 3,
    "not_specified|Nephrotic_syndrome_15": 18,
    "Nephrotic_syndrome_15|not_specified|not_provided": 3,
    "not_provided|not_specified|Nephrotic_syndrome_15": 4,
    "not_provided|Nephrotic_syndrome_15": 15,
    "MAGI2-related_disorder|not_provided": 8,
    "MAGI2-related_disorder|not_specified|not_provided": 3,
    "not_provided|MAGI2-related_disorder": 4,
    "MAGI2-related_disorder": 11,
    "Nephrotic_syndrome_15|not_provided": 2,
    "not_specified|Nephrotic_syndrome_15|not_provided": 2,
    "Nephrotic_syndrome_15|not_provided|MAGI2-related_disorder": 1,
    "MAGI2-related_disorder|Nephrotic_syndrome_15": 1,
    "not_provided|Nephrotic_syndrome_15|not_specified": 2,
    "MAGI2-related_disorder|not_specified": 1,
    "not_specified|not_provided|MAGI2-related_disorder": 1,
    "not_provided|not_specified|MAGI2-related_disorder": 1,
    "not_specified|not_provided|Nephrotic_syndrome_15": 2,
    "MAGI2-related_disorder|Nephrotic_syndrome_15|not_specified|not_provided": 2,
    "MAGI2-related_disorder|Nephrotic_syndrome_15|not_provided|not_specified": 1,
    "MAGI2-related_disorder|Nephrotic_syndrome_15|not_provided": 1,
    "GNAI1-related_disorder": 9,
    "Neurodevelopmental_disorder_with_hypotonia|_impaired_speech|_and_behavioral_abnormalities": 19,
    "Neurodevelopmental_disorder_with_hypotonia|_impaired_speech|_and_behavioral_abnormalities|Neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_impaired_speech|_and_behavioral_abnormalities|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_impaired_speech|_and_behavioral_abnormalities": 2,
    "GNAI1_associated_Neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_impaired_speech|_and_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Neurodevelopmental_disorder_with_hypotonia|_impaired_speech|_and_behavioral_abnormalities": 1,
    "not_provided|GNAI1-related_disorder": 1,
    "Platelet-type_bleeding_disorder_10|not_provided": 12,
    "Platelet-type_bleeding_disorder_10": 77,
    "not_provided|Platelet-type_bleeding_disorder_10": 13,
    "CD36-related_disorder": 18,
    "Platelet-type_bleeding_disorder_10|Malaria|_cerebral|_resistance_to": 1,
    "not_provided|CD36-related_disorder": 2,
    "Malaria|_susceptibility_to|Platelet-type_bleeding_disorder_10|Coronary_heart_disease|_susceptibility_to|_7": 2,
    "Platelet-type_bleeding_disorder_10|not_specified": 2,
    "Inherited_bleeding_disorder|_platelet-type|not_specified|Platelet-type_bleeding_disorder_10": 1,
    "Coronary_heart_disease|_susceptibility_to|_7|Malaria|_susceptibility_to|Platelet-type_bleeding_disorder_10": 1,
    "CD36-related_disorder|not_provided": 2,
    "CD36-related_disorder|Platelet-type_bleeding_disorder_10": 6,
    "Inherited_bleeding_disorder|_platelet-type": 1,
    "CD36-related_disorder|not_provided|Platelet-type_bleeding_disorder_10|Coronary_heart_disease|_susceptibility_to|_7|Malaria|_susceptibility_to|not_specified": 1,
    "Platelet-type_bleeding_disorder_10|Malaria|_susceptibility_to|Coronary_heart_disease|_susceptibility_to|_7": 3,
    "See_cases|CD36-related_disorder": 1,
    "CD36-related_disorder|not_provided|Platelet-type_bleeding_disorder_10": 1,
    "CD36-related_disorder|Platelet-type_bleeding_disorder_10|not_provided": 1,
    "CD36-related_disorder|not_specified|not_provided|Platelet-type_bleeding_disorder_10": 1,
    "not_specified|Platelet-type_bleeding_disorder_10|not_provided": 1,
    "Platelet-type_bleeding_disorder_10|CD36-related_disorder": 1,
    "not_specified|Platelet-type_bleeding_disorder_10": 4,
    "CD36-related_disorder|Malaria|_susceptibility_to|Coronary_heart_disease|_susceptibility_to|_7|Platelet-type_bleeding_disorder_10": 1,
    "Malaria|_susceptibility_to|Platelet-type_bleeding_disorder_10": 1,
    "Platelet-type_bleeding_disorder_10|CD36-related_disorder|not_provided": 2,
    "CD36-related_disorder|Platelet-type_bleeding_disorder_10|not_specified": 1,
    "Malaria|_cerebral|_susceptibility_to|not_specified|Platelet-type_bleeding_disorder_10": 1,
    "not_specified|not_provided|Platelet-type_bleeding_disorder_10": 1,
    "not_provided|Osteopetrosis|Platelet-type_bleeding_disorder_10": 1,
    "not_provided|CD36-related_disorder|Platelet-type_bleeding_disorder_10": 1,
    "Coronary_heart_disease|_susceptibility_to|_7|Platelet-type_bleeding_disorder_10|Malaria|_susceptibility_to|not_provided|CD36-related_disorder": 1,
    "not_provided|not_specified|Platelet-type_bleeding_disorder_10": 1,
    "not_provided|Platelet-type_bleeding_disorder_10|CD36-related_disorder": 1,
    "SEMA3C-related_disorder": 142,
    "not_specified|SEMA3C-related_disorder": 18,
    "not_provided|SEMA3C-related_disorder": 9,
    "not_provided|SEMA3C-related_disorder|not_specified": 1,
    "SEMA3C-related_disorder|not_specified": 7,
    "not_specified|not_provided|SEMA3C-related_disorder": 1,
    "SEMA3C-related_disorder|not_provided": 6,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_39": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_39": 4,
    "HGF-related_disorder|not_provided": 1,
    "not_provided|Nonsyndromic_Hearing_Loss|_Mixed|Autosomal_recessive_nonsyndromic_hearing_loss_39|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_39|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_39|not_specified": 1,
    "not_provided|not_specified|Nonsyndromic_Hearing_Loss|_Mixed": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_39|not_provided": 1,
    "Sensorineural_hearing_loss_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_39": 1,
    "not_provided|Nonsyndromic_Hearing_Loss|_Mixed|not_specified": 1,
    "not_specified|Nonsyndromic_Hearing_Loss|_Mixed|not_provided": 1,
    "not_specified|not_provided|HGF-related_disorder|Nonsyndromic_Hearing_Loss|_Mixed": 1,
    "HGF-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_39|not_provided|HGF-related_disorder": 1,
    "not_specified|Nonsyndromic_Hearing_Loss|_Mixed": 1,
    "Cardiovascular_phenotype|Developmental_and_epileptic_encephalopathy_110": 1,
    "not_specified|Brugada_syndrome|CACNA2D1-related_disorder": 1,
    "Brugada_syndrome|Short_QT_syndrome": 1,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype|not_provided|CACNA2D1-related_disorder": 1,
    "Brugada_syndrome|not_provided|Cardiovascular_phenotype|CACNA2D1-related_disorder": 1,
    "not_provided|Brugada_syndrome|CACNA2D1-related_disorder": 2,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Cardiac_arrest": 1,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome|CACNA2D1-related_disorder|not_provided": 1,
    "CACNA2D1-related_disorder": 5,
    "not_provided|CACNA2D1-related_disorder|Cardiovascular_phenotype|Brugada_syndrome": 2,
    "not_provided|not_specified|CACNA2D1-related_disorder|Brugada_syndrome": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|not_provided|not_specified|CACNA2D1-related_disorder": 1,
    "Brugada_syndrome_1|not_provided|Brugada_syndrome|Ventricular_fibrillation|Breast_carcinoma|Paroxysmal_atrial_fibrillation|Cardiac_arrest|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|CACNA2D1-related_disorder|not_provided|Brugada_syndrome": 1,
    "Brugada_syndrome|Short_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Developmental_and_epileptic_encephalopathy_110": 4,
    "not_specified|not_provided|Cardiovascular_phenotype|CACNA2D1-related_disorder": 1,
    "Cardiovascular_phenotype|CACNA2D1-related_disorder|Brugada_syndrome|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_110|Cardiovascular_phenotype": 1,
    "CACNA2D1-related_disorder|Cardiovascular_phenotype|not_provided|Brugada_syndrome": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|CACNA2D1-related_disorder|not_provided": 1,
    "PCLO-related_disorder|not_provided": 29,
    "Pontocerebellar_hypoplasia_type_3": 21,
    "PCLO-related_disorder": 13,
    "PCLO-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_3": 19,
    "not_provided|not_specified|Pontocerebellar_hypoplasia_type_3": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_3|not_specified": 2,
    "not_provided|PCLO-related_disorder": 23,
    "not_provided|Inborn_genetic_diseases|PCLO-related_disorder": 4,
    "not_provided|Pontocerebellar_hypoplasia_type_3|Inborn_genetic_diseases": 2,
    "Pontocerebellar_hypoplasia_type_3|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|PCLO-related_disorder|Inborn_genetic_diseases": 3,
    "Pontocerebellar_hypoplasia_type_3|not_provided": 7,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_3": 2,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia_type_3": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_3|Inborn_genetic_diseases|PCLO-related_disorder": 1,
    "PCLO-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_3": 2,
    "not_provided|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_3": 1,
    "not_provided|not_specified|PCLO-related_disorder": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_3|PCLO-related_disorder": 2,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_3|not_provided": 2,
    "Inborn_genetic_diseases|PCLO-related_disorder|not_provided": 1,
    "PCLO-related_disorder|Pontocerebellar_hypoplasia_type_3|Inborn_genetic_diseases|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_3|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_3|PCLO-related_disorder|not_specified": 1,
    "PCLO-related_disorder|not_provided|Pontocerebellar_hypoplasia_type_3": 1,
    "PCLO-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Pontocerebellar_hypoplasia_type_3|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|PCLO-related_disorder": 1,
    "PCLO-related_disorder|not_specified|not_provided": 1,
    "PCLO-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_3": 1,
    "PCLO-related_disorder|not_provided|not_specified": 1,
    "Pontocerebellar_hypoplasia_type_3|not_provided|PCLO-related_disorder": 1,
    "PCLO-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_3|not_specified|not_provided": 1,
    "SEMA3E-related_disorder|CHARGE_syndrome": 48,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|CHARGE_syndrome": 3,
    "CHARGE_syndrome|not_provided": 78,
    "SEMA3E-related_disorder": 74,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 14,
    "SEMA3E-related_disorder|not_provided|CHARGE_syndrome": 2,
    "not_provided|CHARGE_syndrome": 168,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_specified": 4,
    "not_specified|CHARGE_syndrome": 24,
    "SEMA3E-related_disorder|not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|CHARGE_syndrome": 1,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|SEMA3E-related_disorder|not_provided": 1,
    "CHARGE_syndrome|SEMA3E-related_disorder": 34,
    "not_specified|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 3,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|CHARGE_syndrome|not_provided|not_specified": 1,
    "CHARGE_syndrome|not_specified": 12,
    "SEMA3E-related_disorder|CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 3,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|SEMA3E-related_disorder|not_specified": 1,
    "SEMA3E-related_disorder|not_provided|not_specified|CHARGE_syndrome": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided": 2,
    "not_provided|SEMA3E-related_disorder|not_specified": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|SEMA3E-related_disorder": 6,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided|SEMA3E-related_disorder": 2,
    "CHARGE_syndrome|SEMA3E-related_disorder|not_provided": 2,
    "Dilated_cardiomyopathy_1A|SEMA3E-related_disorder": 1,
    "not_provided|SEMA3E-related_disorder|CHARGE_syndrome": 2,
    "not_provided|SEMA3E-related_disorder|not_specified|CHARGE_syndrome": 1,
    "not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|CHARGE_syndrome": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|CHARGE_syndrome|not_provided": 1,
    "CHARGE_syndrome|SEMA3E-related_disorder|not_specified": 3,
    "Isolated_anophthalmia-microphthalmia_syndrome|CHARGE_syndrome": 1,
    "not_provided|CHARGE_syndrome|SEMA3E-related_disorder|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "not_specified|SEMA3E-related_disorder|CHARGE_syndrome": 2,
    "CHARGE_syndrome|not_provided|SEMA3E-related_disorder": 2,
    "not_specified|not_provided|CHARGE_syndrome": 10,
    "not_specified|CHARGE_syndrome|SEMA3E-related_disorder": 2,
    "CHARGE_syndrome|not_specified|not_provided": 2,
    "CHARGE_syndrome|SEMA3E-related_disorder|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 4,
    "not_specified|not_provided|CHARGE_syndrome|SEMA3E-related_disorder|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_specified|not_provided|SEMA3E-related_disorder": 1,
    "CHARGE_syndrome|SEMA3E-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|CHARGE_syndrome": 3,
    "SEMA3E-related_disorder|CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_specified": 1,
    "not_provided|SEMA3E-related_disorder": 2,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_specified|SEMA3E-related_disorder": 2,
    "not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 3,
    "CHARGE_syndrome|Amenorrhea|SEMA3E-related_disorder": 1,
    "SEMA3E-related_disorder|CHARGE_syndrome|not_specified|not_provided": 1,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|SEMA3E-related_disorder|not_specified": 1,
    "SEMA3E-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "SEMA3E-related_disorder|not_specified|CHARGE_syndrome": 1,
    "SEMA3E-related_disorder|not_provided": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided|SEMA3E-related_disorder|not_specified": 1,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|SEMA3E-related_disorder": 1,
    "not_specified|CHARGE_syndrome|not_provided|SEMA3E-related_disorder": 1,
    "SEMA3A-related_disorder": 114,
    "not_provided|SEMA3A-related_disorder": 13,
    "Inborn_genetic_diseases|SEMA3A-related_disorder": 18,
    "Hypogonadotropic_hypogonadism_16_with_or_without_anosmia|SEMA3A-related_disorder|not_provided": 2,
    "not_provided|Martsolf_syndrome_1": 1,
    "SEMA3A-related_disorder|not_provided": 17,
    "SEMA3A-related_disorder|Delayed_puberty|not_provided": 1,
    "SEMA3A-related_disorder|not_provided|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia": 2,
    "SEMA3A-related_disorder|Inborn_genetic_diseases": 6,
    "SEMA3A-related_disorder|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_16_with_or_without_anosmia": 7,
    "Inborn_genetic_diseases|SEMA3A-related_disorder|not_provided": 1,
    "SEMA3A-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|SEMA3A-related_disorder": 1,
    "SEMA3A-related_disorder|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|not_provided": 1,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia": 1,
    "not_provided|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia": 1,
    "not_provided|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia|SEMA3A-related_disorder": 1,
    "not_provided|not_specified|SEMA3A-related_disorder": 1,
    "SEMA3A-related_disorder|not_provided|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia|Amenorrhea": 1,
    "SEMA3A-related_disorder|Hypogonadotropic_hypogonadism_16_with_or_without_anosmia": 1,
    "SEMA3A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|SEMA3D-related_disorder": 15,
    "SEMA3D-related_disorder": 141,
    "SEMA3D-related_disorder|not_provided": 10,
    "not_specified|SEMA3D-related_disorder": 15,
    "SEMA3D-related_disorder|not_specified": 14,
    "SEMA3D-related_disorder|Progressive_sensorineural_hearing_impairment": 1,
    "not_provided|Aganglionic_megacolon|SEMA3D-related_disorder": 1,
    "SEMA3D-related_disorder|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "ABCB4-related_disorder": 44,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3": 4,
    "Progressive_familial_intrahepatic_cholestasis_type_3": 33,
    "ABCB4-related_disorder|not_provided": 25,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 16,
    "not_provided|ABCB4-related_disorder": 25,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3": 14,
    "Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3": 4,
    "ABCB4-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|ABCB4-related_disorder": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided": 4,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|not_specified": 6,
    "Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|Progressive_familial_intrahepatic_cholestasis|not_provided|ABCB4-related_disorder": 1,
    "not_specified|not_provided|Low_phospholipid_associated_cholelithiasis": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3": 3,
    "ABCB4-related_disorder|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3": 11,
    "not_specified|ABCB4-related_disorder|not_provided": 1,
    "ABCB4-related_disorder|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|Low_phospholipid_associated_cholelithiasis": 1,
    "ABCB4-related_disorder|Inborn_genetic_diseases|Low_phospholipid_associated_cholelithiasis": 1,
    "not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder": 1,
    "not_specified|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Low_phospholipid_associated_cholelithiasis": 7,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided": 1,
    "Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided|ABCB4-related_disorder": 1,
    "ABCB4-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_3|not_provided": 3,
    "not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|ABCB4-Related_Intrahepatic_Cholestasis|Progressive_familial_intrahepatic_cholestasis": 1,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Progressive_familial_intrahepatic_cholestasis|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Inborn_genetic_diseases|not_provided": 1,
    "ABCB4-related_disorder|not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1|Severe_early-childhood-onset_retinal_dystrophy|Progressive_familial_intrahepatic_cholestasis_type_3|See_cases|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "ABCB4-Related_Intrahepatic_Cholestasis|Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|ABCB4-related_disorder": 2,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3": 2,
    "Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided": 1,
    "Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3": 4,
    "not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided": 2,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|not_specified|not_provided": 1,
    "not_specified|ABCB4-related_disorder": 2,
    "Inborn_genetic_diseases|Cholestasis|_intrahepatic|_of_pregnancy|_3": 2,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 5,
    "not_provided|ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3": 2,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis": 2,
    "ABCB4-related_disorder|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "ABCB4-related_disorder|not_specified|not_provided": 4,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided|ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ABCB4-related_disorder|not_provided": 2,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|ABCB4-related_disorder|not_specified": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|not_specified": 1,
    "ABCB4-related_disorder|Familial_intrahepatic_cholestasis_type_3|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder": 1,
    "ABCB4-related_disorder|not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|not_specified|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|ABCB4-related_disorder|not_provided|Low_phospholipid_associated_cholelithiasis": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_3|not_provided": 1,
    "not_provided|Low_phospholipid_associated_cholelithiasis": 3,
    "not_provided|ABCB4-related_disorder|not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|not_specified": 1,
    "not_specified|Low_phospholipid_associated_cholelithiasis|not_provided": 1,
    "not_specified|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 12,
    "ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Intrahepatic_cholestasis": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis": 1,
    "ABCB4-related_disorder|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1": 95,
    "ABCB4-related_disorder|not_provided|not_specified": 2,
    "ABCB4-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_specified": 1,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|ABCB4-related_disorder|not_provided": 1,
    "Low_phospholipid_associated_cholelithiasis|not_provided": 1,
    "ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "ABCB4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|not_provided": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis": 1,
    "ABCB4-related_disorder|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_provided|Progressive_familial_intrahepatic_cholestasis": 1,
    "Inborn_genetic_diseases|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis|Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "not_provided|ABCB4-related_disorder|not_specified": 1,
    "not_specified|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|not_specified": 1,
    "ABCB4-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "ABCB4-related_disorder|not_provided|See_cases": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Cholestasis|_intrahepatic|_of_pregnancy|_3|ABCB4-related_disorder|not_specified": 1,
    "not_provided|not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "Progressive_familial_intrahepatic_cholestasis|ABCB4-related_disorder|Inborn_genetic_diseases|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_3": 1,
    "ABCB4-related_disorder|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_3|Progressive_familial_intrahepatic_cholestasis_type_3|Low_phospholipid_associated_cholelithiasis|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Inborn_genetic_diseases|not_provided|ABCB4-related_disorder": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_3|Cholestasis|_intrahepatic|_of_pregnancy|_3|Low_phospholipid_associated_cholelithiasis": 1,
    "ABCB1-related_disorder": 12,
    "ABCB1-related_disorder|not_provided": 3,
    "Inflammatory_bowel_disease_13|Tramadol_response": 1,
    "Tramadol_response|ABCB1-related_disorder|not_provided|MDR1_POLYMORPHISM": 1,
    "Encephalopathy|_acute_transient": 2,
    "ABCB1-related_disorder|not_specified|not_provided|Inflammatory_bowel_disease_13|Tramadol_response": 1,
    "ABCB1-related_disorder|not_specified|not_provided": 1,
    "not_provided|ABCB1-related_disorder": 2,
    "ABCB1-related_disorder|not_specified|not_provided|Tramadol_response": 1,
    "not_specified|not_provided|ABCB1-related_disorder": 1,
    "COLCHICINE_RESISTANCE": 1,
    "Tramadol_response|ABCB1-related_disorder": 2,
    "Inflammatory_bowel_disease_13": 3,
    "SLC25A40-related_disorder": 3,
    "not_provided|SLC25A40-related_disorder": 1,
    "not_provided|ADAM22-related_disorder": 6,
    "ADAM22-related_disorder|not_provided": 8,
    "not_provided|Developmental_and_epileptic_encephalopathy|_61": 2,
    "ADAM22-related_disorder": 12,
    "Developmental_and_epileptic_encephalopathy|_61|not_provided": 3,
    "not_provided|ADAM22-related_disorder|See_cases": 1,
    "Developmental_and_epileptic_encephalopathy|_61": 11,
    "not_provided|Inborn_genetic_diseases|ADAM22-related_disorder": 1,
    "STEAP1-related_disorder|not_provided": 1,
    "STEAP2-related_disorder": 5,
    "CFAP69-related_disorder": 6,
    "CFAP69-related_disorder|not_provided": 5,
    "not_provided|CFAP69-related_disorder": 1,
    "CFAP69-related_disorder|not_specified": 1,
    "Spermatogenic_failure_24": 4,
    "Spermatogenic_failure_24|not_provided": 2,
    "CFAP69-related_disorder|Spermatogenic_failure_24|not_provided": 1,
    "Spermatogenic_failure_24|not_provided|CFAP69-related_disorder": 1,
    "Spermatogenic_failure_24|CFAP69-related_disorder|not_provided": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided": 9,
    "Long_QT_syndrome_11|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome_11|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_11|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome_11|Long_QT_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 2,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|Cardiovascular_phenotype|not_specified": 1,
    "Long_QT_syndrome_11|Cardiovascular_phenotype|Long_QT_syndrome": 10,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_11": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Atrial_fibrillation|Heart_failure|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Long_QT_syndrome_11|Long_QT_syndrome|Cardiovascular_phenotype": 9,
    "Long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype": 21,
    "Long_QT_syndrome_11|AKAP9-related_disorder|Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_11": 4,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Long_QT_syndrome_11": 3,
    "Cardiovascular_phenotype|Brugada_syndrome|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Brugada_syndrome_1|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_11|Long_QT_syndrome": 20,
    "Long_QT_syndrome_11|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|AKAP9-related_disorder|Cardiovascular_phenotype": 5,
    "Long_QT_syndrome_11|Cardiovascular_phenotype|Long_QT_syndrome|not_specified": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_11|Long_QT_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11": 11,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Long_QT_syndrome_11": 2,
    "Congenital_long_QT_syndrome|Long_QT_syndrome": 48,
    "Long_QT_syndrome_11|not_provided|not_specified|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype|AKAP9-related_disorder": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_11": 14,
    "Long_QT_syndrome_11|Long_QT_syndrome": 13,
    "not_specified|Long_QT_syndrome|Long_QT_syndrome_11|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrest|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome_11": 16,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome": 8,
    "not_provided|AKAP9-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_11|not_specified|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|Cardiovascular_phenotype|Colorectal_cancer|not_specified": 1,
    "AKAP9-related_disorder|Long_QT_syndrome|Long_QT_syndrome_11|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_11": 25,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_11|Long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "AKAP9-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 5,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 7,
    "not_provided|Long_QT_syndrome_11|not_specified|AKAP9-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome": 3,
    "Cardiovascular_phenotype|not_provided|AKAP9-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome": 2,
    "not_specified|Long_QT_syndrome_11|not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|AKAP9-related_disorder|Long_QT_syndrome|not_specified": 1,
    "AKAP9-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome_11": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_11|not_provided|Long_QT_syndrome": 2,
    "not_specified|not_provided|Long_QT_syndrome_11|Long_QT_syndrome|Congenital_long_QT_syndrome": 3,
    "Long_QT_syndrome_1|Long_QT_syndrome": 9,
    "not_specified|Cardiovascular_phenotype|AKAP9-related_disorder|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_11": 4,
    "not_specified|Cardiovascular_phenotype|AKAP9-related_disorder|Long_QT_syndrome|Ventricular_tachycardia|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Primary_dilated_cardiomyopathy|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "AKAP9-related_disorder|Cardiovascular_phenotype|Ventricular_fibrillation|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome_11|Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome": 10,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype|Long_QT_syndrome_11": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome": 7,
    "Long_QT_syndrome_11|not_provided": 7,
    "Long_QT_syndrome|Long_QT_syndrome_11|not_specified": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|Long_QT_syndrome_11|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|AKAP9-related_disorder|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_11|AKAP9-related_disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_provided|not_specified|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_11|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "AKAP9-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|AKAP9-related_disorder": 3,
    "AKAP9-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|not_specified": 4,
    "not_provided|Long_QT_syndrome_11|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|AKAP9-related_disorder|Long_QT_syndrome_11|not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "AKAP9-related_disorder": 5,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_11|AKAP9-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Ventricular_fibrillation|Long_QT_syndrome|not_specified": 1,
    "not_provided|Long_QT_syndrome|not_specified|Cardiac_arrhythmia": 2,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|not_specified|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 2,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|AKAP9-related_disorder": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiomyopathy": 1,
    "not_provided|AKAP9-related_disorder|not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome_11|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome_11|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome_11|Long_QT_syndrome": 2,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_11|not_specified": 1,
    "unspecified_heart_condition|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Cardiovascular_phenotype|AKAP9-related_disorder|not_specified|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|AKAP9-related_disorder": 2,
    "AKAP9-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Sudden_cardiac_death|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "not_provided|Long_QT_syndrome_11|AKAP9-related_disorder|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_11|Long_QT_syndrome|not_specified": 1,
    "Long_QT_syndrome_11|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|AKAP9-related_disorder|Cardiovascular_phenotype": 2,
    "AKAP9-related_disorder|Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 2,
    "AKAP9-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Long_QT_syndrome|not_provided": 1,
    "AKAP9-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome_11|not_specified|not_provided|Long_QT_syndrome": 1,
    "Cardiomyopathy|Long_QT_syndrome_11": 1,
    "not_provided|not_specified|Long_QT_syndrome_11|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|not_specified|Long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|not_provided|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|AKAP9-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Long_QT_syndrome|not_provided|not_specified|Long_QT_syndrome_11": 1,
    "AKAP9-related_disorder|Long_QT_syndrome_11|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Long_QT_syndrome_11|not_specified": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|Congenital_long_QT_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Long_QT_syndrome": 3,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia": 2,
    "Long_QT_syndrome|Heart_failure|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|AKAP9-related_disorder|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome_11|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 11,
    "not_provided|AKAP9-related_disorder|Long_QT_syndrome|Long_QT_syndrome_11|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|AKAP9-related_disorder|not_specified": 1,
    "not_provided|Long_QT_syndrome_11": 2,
    "Long_QT_syndrome_11|not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "AKAP9-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome_11|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Restrictive_cardiomyopathy|not_provided|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome|not_provided|not_specified|Long_QT_syndrome_11|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_11|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|not_specified|Long_QT_syndrome_11|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "AKAP9-related_disorder|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Ventricular_fibrillation|Cardiomyopathy|Long_QT_syndrome_11|not_provided|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype|AKAP9-related_disorder": 1,
    "not_provided|Long_QT_syndrome_11|Long_QT_syndrome": 2,
    "Long_QT_syndrome|not_specified|Long_QT_syndrome_11|Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|not_specified": 1,
    "AKAP9-related_disorder|Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_11|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome_11|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_11|not_specified|Cardiomyopathy|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_11|Long_QT_syndrome_1": 1,
    "not_specified|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_11|AKAP9-related_disorder": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern": 1,
    "Long_QT_syndrome_11|not_provided|Long_QT_syndrome|not_specified|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "AKAP9-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|Long_QT_syndrome_11": 1,
    "not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_11|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_11|not_specified": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|AKAP9-related_disorder": 2,
    "not_provided|Long_QT_syndrome_11|Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome_11|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_11|Congenital_long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Long_QT_syndrome_11|not_provided|not_specified|Primary_dilated_cardiomyopathy|Amyloidosis|Cardiovascular_phenotype": 1,
    "Wolff-Parkinson-White_pattern|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "AKAP9-related_disorder|Long_QT_syndrome_11|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|AKAP9-related_disorder|not_provided|Long_QT_syndrome|Long_QT_syndrome_11": 1,
    "Long_QT_syndrome_11|not_provided|Long_QT_syndrome": 1,
    "Cardiac_arrest|Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|not_specified|AKAP9-related_disorder": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Long_QT_syndrome": 1,
    "CYP51A1-related_disorder": 4,
    "not_provided|CYP51A1-related_disorder": 1,
    "CYP51A1-related_disorder|not_provided": 2,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation": 39,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|not_provided": 4,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|not_provided|Cerebral_cavernous_malformation": 1,
    "Cerebral_cavernous_malformation|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas": 18,
    "not_provided|Cerebral_cavernous_malformation|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas": 4,
    "not_provided|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation": 3,
    "Cerebral_cavernous_malformation|not_provided|KRIT1-related_disorder|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas": 2,
    "not_provided|KRIT1-related_disorder|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation": 1,
    "KRIT1-related_disorder": 16,
    "Inborn_genetic_diseases|Cerebral_cavernous_malformation": 14,
    "KRIT1-related_disorder|not_provided": 1,
    "Cerebral_cavernous_malformation|not_provided|Inborn_genetic_diseases": 1,
    "Cerebral_cavernous_malformation|not_provided": 32,
    "Cerebral_cavernous_malformation|Inborn_genetic_diseases|not_provided": 3,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|KRIT1-related_disorder|not_provided": 1,
    "Cerebral_cavernous_malformation|Inborn_genetic_diseases": 15,
    "not_provided|Cerebral_cavernous_malformation|Inborn_genetic_diseases|KRIT1-related_disorder": 1,
    "not_provided|Cerebral_cavernous_malformation": 39,
    "Cerebral_cavernous_malformation|not_specified|not_provided": 3,
    "not_specified|Cerebral_cavernous_malformation|not_provided|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas": 1,
    "KRIT1-related_disorder|Cerebral_cavernous_malformation|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|not_provided": 1,
    "not_specified|Cerebral_cavernous_malformation": 1,
    "not_provided|Cerebral_cavernous_malformation|not_specified": 1,
    "Cerebral_cavernous_malformation|Cerebral_cavernous_malformation_1": 3,
    "Inborn_genetic_diseases|Cerebral_cavernous_malformation|not_provided": 1,
    "Cerebral_cavernous_malformation|not_specified": 4,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|not_specified|Inborn_genetic_diseases": 1,
    "Cerebral_cavernous_malformation|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Vascular_dementia|not_provided": 2,
    "Cerebral_cavernous_malformation_1|Cerebral_cavernous_malformation": 2,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|not_specified": 1,
    "Cerebral_cavernous_malformation|KRIT1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Cerebral_cavernous_malformation_1|Cerebral_cavernous_malformation|not_provided": 2,
    "KRIT1-related_disorder|not_provided|Cerebral_cavernous_malformation|Cerebral_cavernous_malformation_1": 1,
    "Abnormal_cerebral_vascular_morphology": 1,
    "not_specified|Cerebral_cavernous_malformation|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Inborn_genetic_diseases": 1,
    "not_provided|KRIT1-related_disorder|Cerebral_cavernous_malformation": 1,
    "KRIT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Cerebral_cavernous_malformation|KRIT1-related_disorder": 6,
    "not_provided|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_cavernous_hemangioma_of_brain|Cerebral_cavernous_malformation|not_provided": 1,
    "KRIT1-related_disorder|Cerebral_cavernous_malformation": 1,
    "Cerebral_cavernous_malformation|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Cerebral_cavernous_malformation|not_provided|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation": 1,
    "Cerebral_cavernous_malformation|not_provided|Cavernous_hemangioma": 1,
    "not_provided|Cerebral_cavernous_malformation|KRIT1-related_disorder|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas": 2,
    "KRIT1-related_disorder|not_provided|Cerebral_cavernous_malformation": 1,
    "Hyperkeratotic_cutaneous_capillary-venous_malformations_associated_with_cerebral_capillary_malformations|not_provided": 1,
    "KRIT1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Cerebral_cavernous_malformation|Inborn_genetic_diseases": 1,
    "Cerebral_cavernous_malformation|Inborn_genetic_diseases|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|KRIT1-related_disorder": 1,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|not_specified|Cerebral_cavernous_malformation": 1,
    "not_provided|Cerebral_cavernous_malformation|KRIT1-related_disorder": 1,
    "Cerebral_cavernous_malformation|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "KRIT1-related_disorder|Hereditary_cavernous_hemangioma_of_brain|Inborn_genetic_diseases|not_provided|Cerebral_cavernous_malformation": 1,
    "Cerebral_cavernous_malformation|Cerebral_cavernous_malformation_1|Inborn_genetic_diseases|not_provided": 1,
    "Cerebral_cavernous_malformation|not_provided|Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas": 1,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|Inborn_genetic_diseases": 1,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|Cerebral_cavernous_malformation|KRIT1-related_disorder": 1,
    "Angiokeratoma_corporis_diffusum_with_arteriovenous_fistulas|not_specified|not_provided|Cerebral_cavernous_malformation": 1,
    "Dilated_cardiomyopathy_2B|Cardiovascular_phenotype": 30,
    "Dilated_cardiomyopathy_2B": 75,
    "Dilated_cardiomyopathy_2B|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_2B": 1,
    "GATAD1-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_2B|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_2B": 26,
    "Cardiovascular_phenotype|GATAD1-related_disorder": 1,
    "Dilated_cardiomyopathy_2B|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_2B|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|not_specified|GATAD1-related_disorder|Dilated_cardiomyopathy_2B": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_2B|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_2B": 3,
    "Dilated_cardiomyopathy_2B|not_specified": 2,
    "not_provided|not_specified|Dilated_cardiomyopathy_2B": 1,
    "not_provided|Dilated_cardiomyopathy_2B|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_2B": 2,
    "not_specified|not_provided|Dilated_cardiomyopathy_2B|Cardiovascular_phenotype|GATAD1-related_disorder": 1,
    "not_specified|Dilated_cardiomyopathy_2B|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_2B|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_2B|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_2B|GATAD1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_2B|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_2B|not_provided|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_2B": 1,
    "not_provided|GATAD1-related_disorder": 1,
    "Zellweger_spectrum_disorders|not_provided": 37,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder|Zellweger_spectrum_disorders|not_specified": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 9,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases": 24,
    "PEX1-related_disorder|Zellweger_spectrum_disorders": 19,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|not_specified": 1,
    "Heimler_syndrome_1": 51,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|Zellweger_spectrum_disorders": 2,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|not_provided": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders": 6,
    "PEX1-related_disorder": 20,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1": 7,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1": 16,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 14,
    "Zellweger_spectrum_disorders|PEX1-related_disorder": 20,
    "not_provided|Zellweger_spectrum_disorders|PEX1-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 3,
    "Optic_atrophy|Inborn_genetic_diseases|Zellweger_spectrum_disorders|PEX1-related_disorder": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 20,
    "Peroxisome_biogenesis_disorder_1B|PEX1-related_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Heimler_syndrome_1|not_provided": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 20,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 5,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|not_provided": 1,
    "Heimler_syndrome_1|Zellweger_spectrum_disorders": 7,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1|Zellweger_spectrum_disorders|not_provided": 2,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 4,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 2,
    "not_provided|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder|Heimler_syndrome_1": 1,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 46,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|not_specified|Zellweger_spectrum_disorders": 2,
    "Zellweger_spectrum_disorders|not_provided|not_specified": 2,
    "Zellweger_spectrum_disorders|not_specified|not_provided|PEX1-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Zellweger_spectrum_disorders": 3,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1": 2,
    "not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|not_provided": 3,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|not_provided": 3,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|not_provided|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder_due_to_PEX1_defect|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|not_provided": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 1,
    "Heimler_syndrome_1|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 4,
    "not_provided|Zellweger_spectrum_disorders|PEX1-related_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|PEX1-related_disorder|not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 3,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder|not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1": 1,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1": 2,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 1,
    "not_provided|Inborn_genetic_diseases|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 3,
    "Zellweger_spectrum_disorders|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder_1B": 2,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Retinal_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "Peroxisome_biogenesis_disorder_due_to_PEX1_defect": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Heimler_syndrome_1|not_provided|Peroxisome_biogenesis_disorder_1B": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Inborn_genetic_diseases|not_provided": 1,
    "Zellweger_spectrum_disorders|PEX1-related_disorder|not_specified|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Inborn_genetic_diseases|Heimler_syndrome_1": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|not_specified|PEX1-related_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder|not_specified|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_type_1A|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B": 1,
    "Heimler_syndrome_1|Zellweger_spectrum_disorders|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_due_to_PEX1_defect|Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_specified|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 2,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|not_provided": 1,
    "Zellweger_spectrum_disorders|not_provided|not_specified|PEX1-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders": 6,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "not_specified|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "not_provided|PEX1-related_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "Heimler_syndrome_1|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Microcephaly": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders": 1,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Global_developmental_delay|Very_long_chain_fatty_acid_accumulation|Penile_hypospadias|Polymicrogyria|Seizure": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Retinal_dystrophy|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Heimler_syndrome_1": 3,
    "PEX1-related_disorder|not_provided|Zellweger_spectrum_disorders": 2,
    "not_specified|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|not_provided": 2,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|not_provided|Zellweger_spectrum_disorders": 1,
    "not_provided|not_specified|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|PEX1-related_disorder|not_provided": 1,
    "not_provided|PEX1-related_disorder|Zellweger_spectrum_disorders": 3,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided": 1,
    "Heimler_syndrome_1|not_provided": 1,
    "Heimler_syndrome_1|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder|Abnormality_of_metabolism/homeostasis|Zellweger_spectrum_disorders|See_cases": 1,
    "Zellweger_spectrum_disorders|not_specified|not_provided": 1,
    "Peroxisome_biogenesis_disorder_1B|not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|Heimler_syndrome_1": 1,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "not_specified|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_due_to_PEX1_defect|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1|PEX1-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided|Peroxisome_biogenesis_disorder|Leber_congenital_amaurosis|Peroxisomal_disorder": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1": 2,
    "PEX1-related_disorder|Heimler_syndrome_1|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Zellweger_spectrum_disorders|not_provided": 1,
    "Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 4,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_due_to_PEX1_defect": 1,
    "Zellweger_spectrum_disorders|Optic_atrophy": 2,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 2,
    "not_provided|Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 1,
    "Heimler_syndrome_1|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|not_provided|Heimler_syndrome_1|not_specified": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided": 1,
    "PEX1-related_Peroxisomal_Biogenesis_Disorder|Zellweger_spectrum_disorders|not_provided": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Inborn_genetic_diseases|not_provided|PEX1-related_disorder": 1,
    "Inborn_genetic_diseases|Zellweger_spectrum_disorders|not_provided": 2,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "PEX1-related_disorder|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|Zellweger_spectrum_disorders|Retinal_dystrophy": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Inborn_genetic_diseases|Optic_atrophy|Retinal_dystrophy|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1": 2,
    "Peroxisome_biogenesis_disorder|Heimler_syndrome_1|Zellweger_spectrum_disorders|not_provided": 1,
    "Inborn_genetic_diseases|Heimler_syndrome_1|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided": 2,
    "Zellweger_spectrum_disorders|not_provided|Heimler_syndrome_1": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Inborn_genetic_diseases|PEX1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|PEX1-related_disorder|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|not_provided": 2,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B": 2,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder|PEX1-related_disorder|Zellweger_spectrum_disorders": 1,
    "not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 2,
    "not_specified|Zellweger_spectrum_disorders": 2,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Zellweger_spectrum_disorders|Retinal_dystrophy": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|Heimler_syndrome_1": 1,
    "Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Retinal_dystrophy": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|Heimler_syndrome_1": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|PEX1-related_disorder|Heimler_syndrome_1": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|not_provided|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|not_provided|PEX1-related_disorder": 1,
    "Zellweger_spectrum_disorders|not_provided|PEX1-related_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "not_specified|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|PEX1-related_disorder|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Retinal_dystrophy|Zellweger_spectrum_disorders": 1,
    "not_provided|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 2,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|not_provided": 1,
    "Heimler_syndrome_1|not_specified": 1,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder|PEX1-related_disorder|not_provided|Heimler_syndrome_1|Zellweger_spectrum_disorders": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B": 1,
    "Heimler_syndrome_1|not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_due_to_PEX1_defect|Heimler_syndrome_1": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|not_specified": 1,
    "Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1": 1,
    "Zellweger_spectrum_disorders|not_specified|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 2,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|not_specified": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Zellweger_spectrum_disorders": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Inborn_genetic_diseases|PEX1-related_disorder|not_provided|Peroxisome_biogenesis_disorder": 1,
    "not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|not_provided": 1,
    "not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1": 1,
    "Peroxisome_biogenesis_disorder|PEX1-related_disorder|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|PEX1-related_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Heimler_syndrome_1|Inborn_genetic_diseases|Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_1B|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder|Heimler_syndrome_1": 1,
    "Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder_1B": 1,
    "Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders": 1,
    "not_specified|Peroxisome_biogenesis_disorder_1B|not_provided|Zellweger_spectrum_disorders|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_provided|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_1B|not_provided|Heimler_syndrome_1": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided": 1,
    "PEX1-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder": 1,
    "Heimler_syndrome_1|not_provided|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1": 1,
    "Peroxisome_biogenesis_disorder_1B|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Heimler_syndrome_1|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_type_1A": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder_1B|Heimler_syndrome_1|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|Heimler_syndrome_1|Peroxisome_biogenesis_disorder_1B": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|not_provided|Zellweger_spectrum_disorders": 2,
    "CDK6-related_disorder|not_specified|not_provided": 2,
    "Microcephaly_12|_primary|_autosomal_recessive": 1,
    "not_provided|CDK6-related_disorder": 1,
    "SAMD9-related_disorder": 13,
    "not_provided|Inborn_genetic_diseases|SAMD9-related_disorder": 8,
    "SAMD9-related_disorder|MIRAGE_syndrome|Normophosphatemic_familial_tumoral_calcinosis|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|not_specified|not_provided": 2,
    "SAMD9-related_disorder|not_provided": 11,
    "SAMD9-related_disorder|not_specified|not_provided|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "MIRAGE_syndrome": 13,
    "Inborn_genetic_diseases|SAMD9-related_disorder|not_provided": 5,
    "not_provided|not_specified|SAMD9-related_disorder|Inborn_genetic_diseases": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|not_provided": 2,
    "not_provided|MIRAGE_syndrome": 4,
    "not_provided|Normophosphatemic_familial_tumoral_calcinosis|not_specified": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "SAMD9-related_disorder|Inborn_genetic_diseases|not_provided": 7,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 10,
    "Inborn_genetic_diseases|SAMD9-related_disorder": 6,
    "Normophosphatemic_familial_tumoral_calcinosis|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Myelodysplastic_syndrome": 1,
    "Inborn_genetic_diseases|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|MIRAGE_syndrome|Normophosphatemic_familial_tumoral_calcinosis|not_provided": 1,
    "not_provided|SAMD9-related_disorder": 9,
    "SAMD9-related_disorder|Inborn_genetic_diseases": 3,
    "SAMD9-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "not_provided|Normophosphatemic_familial_tumoral_calcinosis": 4,
    "not_specified|not_provided|SAMD9-related_disorder|MIRAGE_syndrome": 1,
    "Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|not_specified|not_provided|SAMD9-related_disorder": 1,
    "Inborn_genetic_diseases|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "not_specified|SAMD9-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|SAMD9-related_disorder": 1,
    "not_provided|SAMD9-related_disorder|Inborn_genetic_diseases": 5,
    "MIRAGE_syndrome|not_provided": 7,
    "MIRAGE_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "SAMD9-related_disorder|not_provided|Inborn_genetic_diseases": 6,
    "Normophosphatemic_familial_tumoral_calcinosis|SAMD9-related_disorder|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|not_specified|not_provided": 1,
    "MIRAGE_syndrome|Normophosphatemic_familial_tumoral_calcinosis|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "MIRAGE_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|SAMD9-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|SAMD9-related_disorder": 3,
    "Normophosphatemic_familial_tumoral_calcinosis": 4,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_specified|not_provided|SAMD9-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Normophosphatemic_familial_tumoral_calcinosis": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|MIRAGE_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|not_specified|not_provided": 1,
    "not_specified|SAMD9-related_disorder|not_provided": 2,
    "SAMD9-related_disorder|not_provided|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome": 1,
    "Inborn_genetic_diseases|MIRAGE_syndrome|not_provided|SAMD9-related_disorder|Normophosphatemic_familial_tumoral_calcinosis|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "MIRAGE_syndrome|Inborn_genetic_diseases": 2,
    "Normophosphatemic_familial_tumoral_calcinosis|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|MIRAGE_syndrome": 1,
    "not_specified|SAMD9-related_disorder|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "Ataxia-pancytopenia_syndrome": 18,
    "not_provided|Inborn_genetic_diseases|SAMD9-related_disorder|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|MIRAGE_syndrome": 1,
    "Normophosphatemic_familial_tumoral_calcinosis|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|MIRAGE_syndrome|not_provided": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_provided": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_specified|not_provided": 1,
    "SAMD9-related_disorder|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|SAMD9-related_disorder": 1,
    "MIRAGE_syndrome|not_provided|SAMD9-related_disorder": 2,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|SAMD9-related_disorder": 1,
    "MIRAGE_syndrome|Inborn_genetic_diseases|Normophosphatemic_familial_tumoral_calcinosis": 1,
    "not_provided|Inborn_genetic_diseases|MIRAGE_syndrome": 2,
    "not_provided|MIRAGE_syndrome|Inborn_genetic_diseases": 1,
    "SAMD9-related_disorder|MIRAGE_syndrome|not_provided": 1,
    "SAMD9-related_disorder|not_provided|MIRAGE_syndrome|not_specified": 1,
    "not_provided|not_specified|Normophosphatemic_familial_tumoral_calcinosis|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|MIRAGE_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hereditary_cancer": 1,
    "Inborn_genetic_diseases|not_provided|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "not_provided|SAMD9-related_disorder|not_specified|Normophosphatemic_familial_tumoral_calcinosis": 1,
    "MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|Inborn_genetic_diseases|not_provided": 1,
    "Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome": 1,
    "SAMD9-related_disorder|not_specified|not_provided": 1,
    "not_provided|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "SAMD9-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Inborn_genetic_diseases|SAMD9-related_disorder": 1,
    "SAMD9-related_disorder|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|not_specified|not_provided": 1,
    "not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Inborn_genetic_diseases": 1,
    "not_specified|MIRAGE_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|SAMD9-related_disorder": 1,
    "Inborn_genetic_diseases|MIRAGE_syndrome": 1,
    "SAMD9-related_disorder|not_provided|Normophosphatemic_familial_tumoral_calcinosis|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2": 1,
    "not_provided|MIRAGE_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Normophosphatemic_familial_tumoral_calcinosis": 1,
    "SAMD9-related_disorder|Monosomy_7_myelodysplasia_and_leukemia_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome": 3,
    "Inborn_genetic_diseases|SAMD9L-related_disorder|not_provided": 3,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1": 3,
    "Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|SAMD9L-related_disorder|Inborn_genetic_diseases": 10,
    "SAMD9L-related_disorder|not_provided|not_specified": 2,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49|not_provided": 2,
    "not_provided|SAMD9L-related_disorder": 4,
    "not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1": 1,
    "Inborn_genetic_diseases|Ataxia-pancytopenia_syndrome|not_provided": 1,
    "SAMD9L-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "not_specified|Inborn_genetic_diseases|SAMD9L-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|SAMD9L-related_disorder": 7,
    "SAMD9L-related_disorder|Ataxia-pancytopenia_syndrome|not_provided|Inborn_genetic_diseases|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1": 1,
    "Spinocerebellar_ataxia_49": 4,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|not_provided": 2,
    "not_provided|Ataxia-pancytopenia_syndrome": 3,
    "not_specified|SAMD9L-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases": 4,
    "not_provided|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases": 2,
    "Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49|not_provided": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Spinocerebellar_ataxia_49|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "not_provided|not_specified|Ataxia-pancytopenia_syndrome": 1,
    "SAMD9L-related_disorder": 9,
    "not_provided|Inborn_genetic_diseases|SAMD9L-related_disorder": 4,
    "SAMD9L-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Spinocerebellar_ataxia_49|Ataxia-pancytopenia_syndrome|not_provided": 2,
    "not_provided|SAMD9L-related_disorder|not_specified|Inborn_genetic_diseases": 2,
    "Ataxia-pancytopenia_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Ataxia-pancytopenia_syndrome": 1,
    "SAMD9L-related_disorder|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Spinocerebellar_ataxia_49|Ataxia-pancytopenia_syndrome": 2,
    "not_provided|Spinocerebellar_ataxia_49|Ataxia-pancytopenia_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|SAMD9L-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SAMD9L-related_disorder": 6,
    "Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|SAMD9L-related_disorder|not_provided": 1,
    "not_provided|SAMD9L-related_disorder|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|SAMD9L-related_disorder|not_provided": 1,
    "not_provided|Ataxia-pancytopenia_syndrome|SAMD9L-related_disorder": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|not_provided|Ataxia-pancytopenia_syndrome": 1,
    "Ataxia-pancytopenia_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome": 2,
    "interferonopathy": 1,
    "SAMD9L-related_disorder|not_provided|Ataxia-pancytopenia_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1": 1,
    "Ataxia-pancytopenia_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Spinocerebellar_ataxia_49|not_specified|SAMD9L-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-pancytopenia_syndrome": 1,
    "Spinocerebellar_ataxia_49|not_provided": 1,
    "Ataxia-pancytopenia_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|SAMD9L-related_disorder|Inborn_genetic_diseases": 1,
    "Microcephaly|not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49|not_specified|not_provided|SAMD9L-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly": 2,
    "Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|not_provided": 4,
    "SAMD9L-related_disorder|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_49": 1,
    "Inborn_genetic_diseases|Ataxia-pancytopenia_syndrome|SAMD9L-related_disorder|not_provided": 1,
    "not_specified|not_provided|SAMD9L-related_disorder": 1,
    "Ataxia-pancytopenia_syndrome|not_specified|Inborn_genetic_diseases|not_provided|SAMD9L-related_disorder": 1,
    "Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49|not_provided|not_specified|Primary_ciliary_dyskinesia_12": 1,
    "SAMD9L-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|SAMD9L-related_disorder|Inborn_genetic_diseases": 1,
    "SAMD9L-related_disorder|not_provided": 4,
    "not_specified|SAMD9L-related_disorder|Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|not_provided": 1,
    "SAMD9L-related_disorder|not_provided|Ataxia-pancytopenia_syndrome": 1,
    "Spinocerebellar_ataxia_49|Ataxia-pancytopenia_syndrome|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|SAMD9L-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome": 1,
    "Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases": 1,
    "Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|not_provided": 1,
    "not_provided|Ataxia-pancytopenia_syndrome|Spinocerebellar_ataxia_49": 1,
    "Ataxia-pancytopenia_syndrome|SAMD9L-related_disorder|not_specified|not_provided": 1,
    "Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases|SAMD9L-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|SAMD9L-related_disorder": 1,
    "not_provided|Spinocerebellar_ataxia_49": 1,
    "not_provided|SAMD9L-related_disorder|Ataxia-pancytopenia_syndrome|Inborn_genetic_diseases": 1,
    "SAMD9L-related_disorder|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|not_provided": 1,
    "not_provided|Ataxia-pancytopenia_syndrome|SAMD9L-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Ataxia-pancytopenia_syndrome": 1,
    "SAMD9L-related_disorder|Inborn_genetic_diseases|Ataxia-pancytopenia_syndrome|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_seizures|_and_neonatal_cholestasis": 5,
    "CALCR-related_disorder": 7,
    "BONE_MINERAL_DENSITY_QUANTITATIVE_TRAIT_LOCUS_15|CALCR-related_disorder|not_provided": 1,
    "Osteoporosis": 6,
    "CALCR-related_disorder|not_provided": 2,
    "Muscular_dystrophy|_congenital|_with_rapid_progression|Progressive_muscle_weakness|Seizure": 1,
    "Muscular_dystrophy|_congenital|_with_rapid_progression|not_provided": 1,
    "Progressive_muscle_weakness|Seizure|Muscular_dystrophy|_congenital|_with_rapid_progression": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 22,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 14,
    "not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 421,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 509,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided": 7,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 22,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 53,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type": 8,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 27,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 18,
    "COL1A2-related_disorder|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 62,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_Imperfecta|_Dominant": 1,
    "Connective_tissue_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 1,
    "COL1A2-related_disorder": 18,
    "COL1A2-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified|not_provided": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified": 10,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|not_specified": 2,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 7,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 3,
    "not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta|COL1A2-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 42,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2": 7,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 13,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 39,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 22,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 3,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 14,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 8,
    "COL1A2-related_disorder|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|not_provided": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal": 84,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|not_provided|Osteogenesis_imperfecta": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 3,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 1,
    "Decreased_body_weight|Short_stature|Global_developmental_delay|Facial_asymmetry|Strabismus|Single_transverse_palmar_crease|Ventricular_septal_defect|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 5,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|not_provided": 6,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|COL1A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta|Connective_tissue_disorder|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 18,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype": 4,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_cardiac_valvular_type": 2,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_provided": 1,
    "COL1A2-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|COL1A2-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 13,
    "Osteogenesis_imperfecta_type_I": 1506,
    "Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 2,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 7,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Connective_tissue_disorder|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|Osteogenesis_imperfecta": 3,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Osteogenesis_imperfecta|_mild": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I": 8,
    "Cardiovascular_phenotype|COL1A2-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided|Postmenopausal_osteoporosis": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 4,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Abnormality_of_the_skeletal_system|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 4,
    "COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided": 3,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 4,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided": 5,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 4,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III": 3,
    "not_provided|Osteogenesis_imperfecta_type_I": 118,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder": 4,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 4,
    "Osteogenesis_imperfecta_type_III|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Connective_tissue_disorder|Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|COL1A2-related_disorder|not_provided|Osteogenesis_imperfecta|Increased_susceptibility_to_fractures": 1,
    "Osteogenesis_imperfecta_type_III|See_cases|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta": 2,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 2,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided": 1,
    "COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 3,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta|Abnormality_of_the_skeletal_system": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|not_provided|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|Ehlers-Danlos_syndrome|not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|COL1A2-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Cardiovascular_phenotype": 1,
    "See_cases|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_classic_type|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|COL1A2-related_disorder|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|not_specified": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_provided": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Osteogenesis_imperfecta|Intellectual_disability|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Ehlers-Danlos_syndrome|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal": 4,
    "Cardiovascular_phenotype|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|Dentinogenesis_imperfecta|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 3,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_specified": 1,
    "Osteogenesis_imperfecta_type_III|not_provided": 4,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal": 3,
    "Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta_type_III": 1,
    "Ehlers-Danlos_syndrome|not_specified|Osteogenesis_imperfecta|not_provided": 1,
    "Osteogenesis_Imperfecta|_Dominant|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Osteogenesis_imperfecta_type_I": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|COL1A2-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|COL1A2-related_disorder": 2,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|not_provided|Osteogenesis_imperfecta": 2,
    "Osteogenesis_imperfecta|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Inborn_genetic_diseases|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|not_specified": 2,
    "Osteogenesis_imperfecta|_perinatal_lethal|not_provided": 6,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_perinatal_lethal|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|COL1A2-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 3,
    "not_provided|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|not_provided|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Osteogenesis_imperfecta|not_specified|not_provided": 3,
    "not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_cardiac_valvular_type": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteoporosis": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta|_perinatal_lethal|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 2,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_specified": 1,
    "Osteoporosis|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_III": 3,
    "COL1A2-related_disorder|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|See_cases|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_III": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Connective_tissue_disorder": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III": 1,
    "Collagen_type_1_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta": 1,
    "Postmenopausal_osteoporosis": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta|COL1A2-related_disorder|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Dentinogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome": 1,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|not_specified|Osteogenesis_imperfecta|Postmenopausal_osteoporosis|Marfan_syndrome|_atypical": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 2,
    "COL1A2-related_disorder|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Osteogenesis_imperfecta_type_I|COL1A2-related_disorder|not_provided": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified": 2,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "not_provided|COL1A2-related_disorder": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 4,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Osteogenesis_imperfecta|Predisposition_to_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|not_specified": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|COL1A2-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided": 1,
    "Multiple_prenatal_fractures|Skeletal_dysplasia": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta|Intellectual_disability|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|COL1A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta": 1,
    "not_provided|Bruck_syndrome_1": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 2,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteoporosis|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_specified|See_cases": 1,
    "Osteogenesis_imperfecta_type_III|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|See_cases": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|COL1A2-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|COL1A2-related_disorder|not_provided": 1,
    "COL1A2-related_disorder|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided|Osteogenesis_imperfecta": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Inborn_genetic_diseases": 1,
    "not_specified|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteoporosis": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided|Osteogenesis_imperfecta": 1,
    "not_specified|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided": 1,
    "Osteogenesis_imperfecta|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Short_fetal_femur_length|See_cases": 1,
    "COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|COL1A2-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Cardiovascular_phenotype|COL1A2-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Dentinogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL1A2-related_disorder|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Osteogenesis_imperfecta_type_III|COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 2,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Rare_disease_with_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|COL1A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|COL1A2-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|COL1A2-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|not_provided": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_specified|COL1A2-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_Imperfecta|_Recessive": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2|Osteoporosis|Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|COL1A2-related_disorder|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|COL1A2-related_disorder": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_2": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_classic_type|_1|COL1A2-related_disorder": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype": 1,
    "See_cases|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2": 2,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_Imperfecta|_Dominant": 1,
    "Myoclonic_dystonia_11": 480,
    "not_provided|Myoclonic_dystonia_11": 35,
    "not_specified|Myoclonic_dystonia_11|Inborn_genetic_diseases": 1,
    "SGCE-related_disorder|not_specified|Myoclonic_dystonia_11|not_provided": 1,
    "Myoclonic_dystonia_11|SGCE-related_disorder|not_provided": 1,
    "not_specified|Myoclonic_dystonia_11|not_provided": 3,
    "not_specified|not_provided|Myoclonic_dystonia_11": 1,
    "SGCE-related_disorder|Myoclonic_dystonia_11": 2,
    "SGCE-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Myoclonic_dystonia_11": 3,
    "not_specified|Myoclonic_dystonia_11": 4,
    "Myoclonic_dystonia_11|Inborn_genetic_diseases": 10,
    "not_provided|Myoclonic_dystonia_11|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Myoclonic_dystonia_11": 7,
    "not_specified|not_provided|Myoclonic_dystonia_11|Inborn_genetic_diseases": 1,
    "Myoclonic_dystonia_11|not_provided": 17,
    "Myoclonic_dystonia_11|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Myoclonic_dystonia_11": 2,
    "not_provided|Myoclonic_dystonia_11|Inborn_genetic_diseases|Movement_disorder": 1,
    "Myoclonic_dystonia_11|not_provided|not_specified": 2,
    "Myoclonus-dystonia_syndrome": 1,
    "not_provided|Myoclonic_dystonia_11|not_specified": 2,
    "Myoclonus-dystonia_syndrome|not_provided|Myoclonic_dystonia_11": 1,
    "Myoclonic_dystonia_11|not_specified": 1,
    "not_provided|not_specified|Myoclonic_dystonia_11": 1,
    "Myoclonic_dystonia_11|not_provided|SGCE-related_disorder": 1,
    "Inborn_genetic_diseases|Myoclonic_dystonia_11|not_provided": 1,
    "Myoclonic_dystonia_11|SGCE-related_disorder": 1,
    "not_specified|Myoclonic_dystonia_11|Inborn_genetic_diseases|not_provided": 1,
    "SGCE-related_disorder|not_provided|Myoclonic_dystonia_11": 1,
    "SGCE-related_disorder|Inborn_genetic_diseases|not_provided|Myoclonic_dystonia_11": 1,
    "SGCE-related_disorder|not_provided": 1,
    "PPP1R9A-related_disorder": 17,
    "PPP1R9A-related_disorder|not_provided": 2,
    "not_provided|PPP1R9A-related_disorder": 3,
    "PPP1R9A-related_disorder|not_specified|not_provided": 1,
    "PON1-related_disorder": 2,
    "PON1-related_disorder|not_provided|Enzyme_activity_finding": 2,
    "not_provided|Enzyme_activity_finding": 1,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis": 1,
    "PARAOXONASE_2_POLYMORPHISM|not_provided": 1,
    "PON2-related_disorder": 3,
    "not_provided|PARAOXONASE_2_POLYMORPHISM": 1,
    "PON2-related_disorder|not_provided": 1,
    "DYNC1I1-related_disorder|not_provided": 6,
    "not_specified|DYNC1I1-related_disorder|not_provided": 2,
    "DYNC1I1-related_disorder": 5,
    "not_provided|DYNC1I1-related_disorder": 1,
    "Citrullinemia_type_II|Citrullinemia_type_I": 10,
    "Citrullinemia_type_II": 11,
    "Citrullinemia_type_I|Citrullinemia_type_II": 6,
    "not_provided|Citrullinemia_type_I|Citrullinemia_type_II": 1,
    "Citrin_deficiency": 484,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 12,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Late-onset_citrullinemia|Citrullinemia_type_I|SLC25A13-related_disorder|not_provided|Inborn_genetic_diseases|Citrin_deficiency|Citrullinemia_type_II": 1,
    "SLC25A13-related_disorder|not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia_type_II|Citrin_deficiency|Citrullinemia_type_I|Late-onset_citrullinemia": 1,
    "SLC25A13-related_disorder|Citrin_deficiency": 5,
    "not_provided|Citrullinemia_type_I|Citrullinemia_type_II|Late-onset_citrullinemia|Citrin_deficiency": 1,
    "Citrullinemia": 453,
    "Citrin_deficiency|not_specified": 3,
    "Citrin_deficiency|not_provided": 10,
    "Citrullinemia|_type_II|_adult-onset": 33,
    "not_specified|Citrin_deficiency|not_provided|Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency|not_provided|Citrullinemia_type_II": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 11,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrin_deficiency": 3,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|not_specified": 1,
    "not_provided|Citrin_deficiency": 3,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|SLC25A13-related_disorder|Citrullinemia|_type_II|_adult-onset|CITRIN_DEFICIENCY|_NEONATAL_ONSET|Citrullinemia|Citrullinemia_type_II": 1,
    "Citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 7,
    "Citrullinemia_type_I|Citrullinemia_type_II|Citrin_deficiency": 2,
    "Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 1,
    "SLC25A13-related_disorder": 13,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency": 13,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia_type_II|not_provided|Citrullinemia|Inborn_genetic_diseases": 1,
    "Citrullinemia|not_provided|Citrin_deficiency": 2,
    "Citrullinemia|SLC25A13-related_disorder|Citrin_deficiency": 1,
    "Citrin_deficiency|SLC25A13-related_disorder": 5,
    "Citrin_deficiency|Inborn_genetic_diseases": 4,
    "SLC25A13-related_disorder|Inborn_genetic_diseases|Citrin_deficiency": 3,
    "not_provided|SLC25A13-related_disorder|Citrin_deficiency": 2,
    "Citrin_deficiency|Late-onset_citrullinemia|not_provided|not_specified|Citrullinemia_type_II": 1,
    "Citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia": 1,
    "not_specified|not_provided|Citrullinemia_type_I|Citrullinemia_type_II|Citrullinemia|Citrin_deficiency": 2,
    "Citrullinemia|_type_II|_adult-onset|SLC25A13-related_disorder|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency|not_provided|Citrullinemia_type_II": 1,
    "Citrullinemia|Citrin_deficiency": 9,
    "not_provided|Citrin_deficiency|Citrullinemia_type_II": 1,
    "SLC25A13-related_disorder|Citrullinemia|Citrin_deficiency": 2,
    "Citrullinemia_type_II|Citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|SLC25A13-related_disorder|not_provided|Citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Citrin_deficiency": 2,
    "Citrin_deficiency|not_provided|SLC25A13-related_disorder|Citrullinemia": 1,
    "Citrullinemia|_type_II|_adult-onset|not_provided": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia|Citrin_deficiency": 1,
    "Citrullinemia|Inborn_genetic_diseases|Citrin_deficiency": 1,
    "not_specified|Citrullinemia": 9,
    "Citrin_deficiency|Late-onset_citrullinemia|not_provided": 1,
    "Citrin_deficiency|not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia_type_II|SLC25A13-related_disorder": 1,
    "SLC25A13-related_disorder|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency": 2,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|SLC25A13-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|SLC25A13-related_disorder": 1,
    "not_provided|not_specified|Citrin_deficiency|Citrullinemia_type_II": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrullinemia|not_provided|not_specified|Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 1,
    "Citrin_deficiency|Citrullinemia_type_II": 5,
    "Inborn_genetic_diseases|Citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrullinemia|Citrin_deficiency|not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 1,
    "Citrullinemia_type_I|Citrullinemia_type_II|Inborn_genetic_diseases": 1,
    "Late-onset_citrullinemia|Citrullinemia_type_II|not_provided|Citrin_deficiency": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|not_specified": 1,
    "Citrullinemia_type_II|Citrullinemia|_type_II|_adult-onset|Late-onset_citrullinemia|Citrin_deficiency|SLC25A13-related_disorder|not_provided": 1,
    "Late-onset_citrullinemia|SLC25A13-related_disorder|Citrin_deficiency": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|SLC25A13-related_disorder|Citrin_deficiency|not_provided": 1,
    "Citrullinemia_type_I|Citrin_deficiency": 2,
    "not_provided|Citrullinemia_type_I|Citrullinemia_type_II|SLC25A13-related_disorder|Citrin_deficiency": 1,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 5,
    "Citrullinemia|_type_II|_adult-onset|Late-onset_citrullinemia|Citrin_deficiency|not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia_type_II": 1,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|not_provided": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia_type_II": 1,
    "SLC25A13-related_disorder|Citrullinemia_type_I|Late-onset_citrullinemia|Citrin_deficiency|not_provided|Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 1,
    "not_provided|Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency|Inborn_genetic_diseases": 1,
    "Citrin_deficiency|SLC25A13-related_disorder|not_specified|not_provided": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 2,
    "Citrullinemia|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 1,
    "not_provided|Citrullinemia_type_I|Citrullinemia|Citrullinemia_type_II|Citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia_type_II": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia_type_II|not_specified|Citrullinemia_type_I|Late-onset_citrullinemia|not_provided|Citrullinemia|_type_II|_adult-onset|Citrin_deficiency": 1,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|SLC25A13-related_disorder|Citrullinemia|_type_II|_adult-onset|CITRIN_DEFICIENCY|_NEONATAL_ONSET|Late-onset_citrullinemia|Citrullinemia_type_II": 1,
    "not_provided|Citrullinemia|_type_II|_adult-onset": 1,
    "Late-onset_citrullinemia|Citrin_deficiency|not_provided": 1,
    "Late-onset_citrullinemia": 2,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia|not_provided": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|not_provided|Citrullinemia_type_II": 1,
    "Late-onset_citrullinemia|Citrullinemia_type_I|Citrullinemia_type_II|Inborn_genetic_diseases|Citrin_deficiency": 1,
    "Citrin_deficiency|Citrullinemia_type_II|Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Late-onset_citrullinemia": 1,
    "Citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia_type_II": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia|Citrullinemia_type_II|Citrin_deficiency": 1,
    "Inborn_genetic_diseases|Citrullinemia": 2,
    "not_provided|Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 1,
    "Citrin_deficiency|Citrullinemia|SLC25A13-related_disorder|not_provided": 1,
    "not_provided|Citrullinemia|Citrin_deficiency": 2,
    "Citrin_deficiency|Citrullinemia": 3,
    "Inborn_genetic_diseases|Citrin_deficiency|not_provided": 1,
    "not_provided|Citrin_deficiency|SLC25A13-related_disorder": 1,
    "SLC25A13-related_disorder|not_provided|Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|CITRIN_DEFICIENCY|_NEONATAL_ONSET|Citrullinemia|_type_II|_adult-onset|Late-onset_citrullinemia|Citrin_deficiency": 1,
    "SLC25A13-related_disorder|Citrin_deficiency|not_specified": 1,
    "SLC25A13-related_disorder|Citrin_deficiency|not_specified|not_provided": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency|not_specified": 1,
    "Citrullinemia_type_I|Citrin_deficiency|SLC25A13-related_disorder|Citrullinemia|_type_II|_adult-onset": 1,
    "SLC25A13-related_disorder|Citrullinemia": 1,
    "Citrullinemia_type_II|not_provided|Citrin_deficiency|SLC25A13-related_disorder|not_specified": 1,
    "Citrullinemia_type_II|Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency": 1,
    "Citrullinemia_type_II|Citrullinemia_type_I|Citrin_deficiency": 2,
    "Inborn_genetic_diseases|Citrullinemia_type_II": 1,
    "not_specified|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 1,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia|Citrullinemia_type_II": 1,
    "Citrin_deficiency|Citrullinemia_type_II|SLC25A13-related_disorder|Late-onset_citrullinemia": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrullinemia": 1,
    "Citrullinemia_type_II|not_provided": 1,
    "Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Late-onset_citrullinemia|SLC25A13-related_disorder|Citrin_deficiency|not_provided|Citrullinemia_type_II": 1,
    "not_provided|Citrullinemia_type_II": 1,
    "Citrin_deficiency|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrullinemia|not_provided": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 1,
    "Citrin_deficiency|Citrullinemia|not_provided": 1,
    "Citrin_deficiency|SLC25A13-related_disorder|Citrullinemia_type_II": 1,
    "Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrin_deficiency|not_provided|Citrullinemia_type_I|Citrullinemia|not_specified|Citrullinemia|_type_II|_adult-onset": 1,
    "not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset|Citrin_deficiency": 1,
    "Late-onset_citrullinemia|Citrin_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|not_specified|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia": 1,
    "SLC25A13-related_disorder|Citrin_deficiency|not_provided|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 1,
    "Citrullinemia_type_II|Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency": 1,
    "Citrin_deficiency|not_specified|not_provided": 1,
    "Citrullinemia|Citrullinemia|_type_II|_adult-onset": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|Citrin_deficiency|not_provided": 1,
    "SLC25A13-related_disorder|not_specified|Citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Citrin_deficiency|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly": 1,
    "Citrullinemia_type_I|Citrullinemia_type_II|SLC25A13-related_disorder|Citrin_deficiency": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Late-onset_citrullinemia|SLC25A13-related_disorder|Citrin_deficiency|not_specified|not_provided|Citrullinemia_type_II|Citrullinemia_type_I": 1,
    "Citrullinemia|_type_II|_adult-onset|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|not_provided": 1,
    "not_provided|Citrullinemia_type_I|Citrin_deficiency": 1,
    "Citrullinemia_type_I|Citrullinemia_type_II|Neonatal_intrahepatic_cholestasis_due_to_citrin_deficiency|Citrullinemia|_type_II|_adult-onset": 1,
    "SEM1-related_disorder": 1,
    "DLX6-related_disorder|not_provided": 4,
    "not_provided|DLX6-related_disorder": 7,
    "DLX6-related_disorder": 6,
    "Split_hand-foot_malformation_1": 4,
    "DLX5-related_disorder": 4,
    "not_provided|Split_hand-foot_malformation_1_with_sensorineural_hearing_loss": 1,
    "not_provided|DLX5-related_disorder": 1,
    "Split_hand-foot_malformation_1_with_sensorineural_hearing_loss|Split_hand-foot_malformation_1": 1,
    "not_provided|Split_hand-foot_malformation_1": 1,
    "DLX5-related_disorder|not_provided": 1,
    "Split_hand-foot_malformation_1_with_sensorineural_hearing_loss": 2,
    "Split_hand-foot_malformation_1|Split_hand-foot_malformation_1_with_sensorineural_hearing_loss": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_provided": 32,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 66,
    "Inborn_genetic_diseases|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_provided": 2,
    "not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 24,
    "not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|Inborn_genetic_diseases": 4,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_provided|ASNS-related_disorder|not_specified": 1,
    "not_specified|not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_specified|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "not_provided|Neurodevelopmental_abnormality|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_specified|ASNS-related_disorder|not_provided": 1,
    "not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|Spinocerebellar_ataxia|_autosomal_recessive_29": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_specified": 2,
    "not_specified|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "Inborn_genetic_diseases|ASNS-related_disorder": 1,
    "not_provided|ASNS-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_specified": 1,
    "ASNS-related_disorder|not_provided|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|ASNS-related_disorder|not_provided": 1,
    "ASNS-related_disorder|not_provided": 2,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|Neurodevelopmental_abnormality|not_provided": 1,
    "not_provided|ASNS-related_disorder|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome": 1,
    "Neurodevelopmental_delay|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_provided": 1,
    "ASNS-related_disorder|not_specified|not_provided": 1,
    "ASNS-related_disorder|Congenital_microcephaly_-_severe_encephalopathy_-_progressive_cerebral_atrophy_syndrome|not_provided": 1,
    "TRRAP-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "TRRAP-related_disorder": 38,
    "Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 87,
    "Hearing_loss|_autosomal_dominant_75|Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 3,
    "not_specified|not_provided|Hearing_loss|_autosomal_dominant_75": 1,
    "not_provided|Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 12,
    "TRRAP-related_disorder|not_provided": 39,
    "Developmental_delay_with_or_without_dysmorphic_facies_and_autism|not_provided": 7,
    "Inborn_genetic_diseases|not_specified|TRRAP-related_disorder": 1,
    "not_provided|TRRAP-related_disorder|See_cases": 1,
    "not_provided|TRRAP-related_disorder": 31,
    "Hearing_loss|_autosomal_dominant_75": 7,
    "not_provided|Developmental_delay_with_or_without_dysmorphic_facies_and_autism|Hearing_loss|_autosomal_dominant_75": 3,
    "Developmental_delay_with_or_without_dysmorphic_facies_and_autism|Inborn_genetic_diseases": 3,
    "not_provided|TRRAP-related_neurodevelopmental_disorder": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_75|Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 1,
    "Developmental_delay_with_or_without_dysmorphic_facies_and_autism|Hearing_loss|_autosomal_dominant_75": 5,
    "TRRAP-related_neurodevelopmental_disorder": 2,
    "Inborn_genetic_diseases|TRRAP-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|TRRAP-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 1,
    "not_provided|TRRAP-related_disorder|Complex_neurodevelopmental_disorder_with_or_without_congenital_anomalies": 1,
    "not_provided|Developmental_delay_with_or_without_dysmorphic_facies_and_autism|TRAPP-associated_developmental_delay": 1,
    "Developmental_delay_with_or_without_dysmorphic_facies_and_autism|TRRAP-related_disorder": 1,
    "not_provided|Complex_neurodevelopmental_disorder_with_or_without_congenital_anomalies": 1,
    "TRRAP-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 1,
    "Teratoma|Developmental_delay_with_or_without_dysmorphic_facies_and_autism": 1,
    "not_provided|Developmental_delay_with_or_without_dysmorphic_facies_and_autism|Inborn_genetic_diseases": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_75|Developmental_delay_with_or_without_dysmorphic_facies_and_autism|Inborn_genetic_diseases": 1,
    "Developmental_delay_with_or_without_dysmorphic_facies_and_autism|Hearing_loss|_autosomal_dominant_75|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_dominant_75|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|TRRAP-related_disorder": 1,
    "TRRAP-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Oocyte/zygote/embryo_maturation_arrest_17": 3,
    "KPNA7-related_disorder|not_provided": 4,
    "Oocyte/zygote/embryo_maturation_arrest_17": 2,
    "not_provided|KPNA7-related_disorder": 10,
    "not_provided|KPNA7-related_disorder|not_specified": 1,
    "Oocyte/zygote/embryo_maturation_arrest_17|not_provided": 2,
    "not_provided|Intellectual_disability|_mild": 1,
    "not_specified|not_provided|KPNA7-related_disorder": 1,
    "Combined_immunodeficiency|Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease": 1,
    "ARPC1B-related_disorder|not_provided": 11,
    "Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease": 11,
    "Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease|not_provided": 3,
    "Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|ARPC1B-related_disorder": 6,
    "Abnormal_bleeding|Thrombocytopenia|not_provided|Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease": 1,
    "not_provided|Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease": 4,
    "not_provided|Inborn_genetic_diseases|Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease": 1,
    "Combined_immunodeficiency|not_provided|Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease": 1,
    "ARPC1B-related_disorder|Platelet_abnormalities_with_eosinophilia_and_immune-mediated_inflammatory_disease|not_provided": 1,
    "not_provided|Kabuki_syndrome_1": 30,
    "CYP3A5-related_disorder": 11,
    "Essential_hypertension": 5,
    "appendicular_lean_mass_relative_to_body_height": 1,
    "Hypertension|_salt-sensitive_essential|_susceptibility_to|refractory_myasthenia_gravis|Tacrolimus_response": 1,
    "CYP3A5-related_disorder|not_provided": 1,
    "Vitamin_D-dependent_rickets|_type_3": 5,
    "fentanyl_response_-_Dosage|tacrolimus_response_-_Metabolism/PK": 1,
    "tacrolimus_response_-_Metabolism/PK": 1,
    "CYP3A4-related_disorder": 1,
    "CYP3A4_PROMOTER_POLYMORPHISM|.|not_provided": 1,
    "GJC3-related_disorder": 6,
    "MCM7-related_disorder|not_provided": 1,
    "Microcephaly|Astigmatism|Anisometropia|Trichiasis|Microphthalmia|Deeply_set_eye|Psychomotor_retardation|Progeroid_facial_appearance|Hypermetropia|Meier-Gorlin_syndrome": 1,
    "MCM7-related_disorder": 1,
    "Hypermetropia|Astigmatism|Trichiasis|Psychomotor_retardation|Anisometropia|Microphthalmia|Deeply_set_eye|Microcephaly|Progeroid_facial_appearance": 1,
    "Hereditary_spastic_paraplegia_50": 229,
    "not_provided|Intellectual_disability|Hereditary_spastic_paraplegia_50": 1,
    "Hereditary_spastic_paraplegia_50|Inborn_genetic_diseases": 12,
    "not_provided|Hereditary_spastic_paraplegia_50": 14,
    "not_provided|Hereditary_spastic_paraplegia_50|Intellectual_disability": 1,
    "AP4M1-related_disorder": 4,
    "Hereditary_spastic_paraplegia_50|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_50": 11,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_50": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_50": 1,
    "Hereditary_spastic_paraplegia_50|not_provided": 9,
    "not_specified|Hereditary_spastic_paraplegia_50": 5,
    "not_provided|Hereditary_spastic_paraplegia_50|Spastic_paraplegia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_50": 1,
    "not_provided|Hereditary_spastic_paraplegia_50|AP4M1-related_disorder": 3,
    "AP4M1-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia_50": 1,
    "AP4M1-related_disorder|Hereditary_spastic_paraplegia_50": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_50|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_50|not_specified": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_50|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_50|not_provided": 3,
    "Hereditary_spastic_paraplegia_50|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "AP-4_deficiency_syndrome|Hereditary_spastic_paraplegia_50|Spastic_paraplegia": 1,
    "AP-4_deficiency_syndrome": 3,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_50": 2,
    "Hereditary_spastic_paraplegia_50|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_50|AP4M1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_50|AP-4_deficiency_syndrome": 1,
    "Hereditary_spastic_paraplegia_50|Spastic_paraplegia": 2,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_50": 1,
    "Hereditary_spastic_paraplegia|not_specified": 3,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Intellectual_disability|not_provided|Hereditary_spastic_paraplegia_50": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_50": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_50": 1,
    "AP4M1-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_50": 1,
    "not_provided|AP4M1-related_disorder|Hereditary_spastic_paraplegia_50|Brain_atrophy|CNS_hypomyelination|Hypoplasia_of_the_corpus_callosum|Microcephaly|Global_developmental_delay|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_50": 1,
    "Hereditary_spastic_paraplegia_50|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_50": 2,
    "Hereditary_spastic_paraplegia_50|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_50|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "Intellectual_disability|Spastic_paraplegia|Hereditary_spastic_paraplegia_50|not_provided": 1,
    "Hereditary_spastic_paraplegia_50|Spastic_paraplegia|AP4M1-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_50|not_specified|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_50": 1,
    "Hereditary_spastic_paraplegia_50|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_50|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_50|Hereditary_spastic_paraplegia|AP4M1-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_50|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_50|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_50|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_50|not_specified|Hereditary_spastic_paraplegia|AP4M1-related_disorder": 1,
    "not_specified|Hereditary_spastic_paraplegia_50|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_50|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_provided|Alazami-Yuan_syndrome": 5,
    "Alazami-Yuan_syndrome": 5,
    "not_provided|TAF6-related_disorder": 5,
    "Alazami-Yuan_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "TAF6-related_disorder|not_provided": 2,
    "TAF6-related_disorder": 3,
    "not_provided|TAF6-related_disorder|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Alazami-Yuan_syndrome": 1,
    "Alazami-Yuan_syndrome|not_provided": 2,
    "Alazami-Yuan_syndrome|Inborn_genetic_diseases|Syndromic_intellectual_disability|not_provided|Intellectual_disability|Global_developmental_delay|Abnormal_facial_shape": 1,
    "Cornelia_de_Lange_syndrome_1|Alazami-Yuan_syndrome": 1,
    "Microcephaly_25|_primary|_autosomal_recessive": 2,
    "Microcephaly_25|_primary|_autosomal_recessive|not_provided": 1,
    "TRAPPC14-related_disorder": 4,
    "not_provided|TRAPPC14-related_disorder": 1,
    "Spermatogenic_failure_61|not_provided|Premature_ovarian_failure_8": 2,
    "Premature_ovarian_failure_8|Spermatogenic_failure_61|not_provided": 1,
    "Premature_ovarian_failure_8": 10,
    "STAG3-related_disorder": 9,
    "Premature_ovarian_failure_8|Spermatogenic_failure_61|PRIMARY_OVARIAN_FAILURE_8": 1,
    "Spermatogenesis_maturation_arrest|Non-obstructive_azoospermia|Spermatogenic_failure_61": 1,
    "Spermatogenic_failure_61|Premature_ovarian_failure_8|not_provided": 1,
    "Spermatogenic_failure_61|Spermatogenesis_maturation_arrest|Non-obstructive_azoospermia": 1,
    "not_provided|STAG3-related_disorder": 2,
    "Premature_ovarian_failure_8|not_provided|Spermatogenic_failure_61": 1,
    "Spermatogenic_failure_61": 2,
    "Premature_ovarian_insufficiency|Non-obstructive_azoospermia": 2,
    "CASTOR3-related_condition": 1,
    "not_provided|CASTOR3-related_condition": 1,
    "not_provided|Spermatogenic_failure_61|Premature_ovarian_failure_8": 1,
    "Premature_ovarian_insufficiency|Female_infertility|Abnormality_of_the_ovary|Premature_ovarian_failure_8|not_provided": 1,
    "PRIMARY_OVARIAN_FAILURE_8": 1,
    "Progressive_microcephaly": 1,
    "PCOLCE-related_disorder": 4,
    "Hemochromatosis_type_3": 135,
    "not_provided|Hemochromatosis_type_3": 2,
    "Hemochromatosis_type_3|Hereditary_hemochromatosis": 59,
    "Hereditary_hemochromatosis|TFR2-related_disorder": 3,
    "Hereditary_hemochromatosis|not_provided|Hemochromatosis_type_3": 6,
    "Hereditary_hemochromatosis|Hemochromatosis_type_3": 57,
    "Inborn_genetic_diseases|Hemochromatosis_type_3": 2,
    "Hereditary_hemochromatosis|not_provided|Inborn_genetic_diseases": 1,
    "Hemochromatosis_type_3|Hereditary_hemochromatosis|TFR2-related_disorder": 3,
    "Hemochromatosis_type_3|not_specified|Hereditary_hemochromatosis|not_provided": 1,
    "Hereditary_hemochromatosis|Inborn_genetic_diseases|Hemochromatosis_type_3": 4,
    "Hereditary_hemochromatosis|Hemochromatosis_type_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_hemochromatosis|Hemochromatosis_type_3": 1,
    "Hemochromatosis_type_1|Hereditary_hemochromatosis|Hemochromatosis_type_3": 1,
    "not_provided|Hemochromatosis_type_3|Hereditary_hemochromatosis": 3,
    "Inborn_genetic_diseases|Hemochromatosis_type_3|Hereditary_hemochromatosis": 3,
    "Hereditary_hemochromatosis|TFR2-related_disorder|Hemochromatosis_type_3": 2,
    "not_specified|Hereditary_hemochromatosis_type_4|not_provided|Hemochromatosis_type_3|Hereditary_hemochromatosis": 1,
    "Hereditary_hemochromatosis_type_5|Hereditary_hemochromatosis": 1,
    "Hemochromatosis_type_3|not_provided|Hereditary_hemochromatosis": 1,
    "not_provided|Hereditary_hemochromatosis|Hemochromatosis_type_3|TFR2-related_disorder": 1,
    "Hereditary_hemochromatosis|Hemochromatosis_type_3|not_provided|Inborn_genetic_diseases": 1,
    "Hemochromatosis_type_3|Inborn_genetic_diseases|Hereditary_hemochromatosis": 2,
    "not_provided|TFR2-related_disorder|Hereditary_hemochromatosis|Hemochromatosis_type_3": 1,
    "Hereditary_hemochromatosis|Hemochromatosis_type_3|not_specified": 1,
    "TFR2-related_disorder|Hereditary_hemochromatosis|not_provided|Hemochromatosis_type_3|Hemochromatosis|_type_1|_modifier_of": 1,
    "Inborn_genetic_diseases|Hereditary_hemochromatosis|Hemochromatosis_type_3": 1,
    "not_specified|Hemochromatosis_type_3": 1,
    "not_provided|Hemochromatosis_type_1|Hereditary_hemochromatosis|Hemochromatosis_type_3": 1,
    "Hereditary_hemochromatosis|not_specified|Hemochromatosis_type_3": 1,
    "TFR2-related_disorder": 4,
    "Hemochromatosis_type_3|Hereditary_hemochromatosis|not_provided": 1,
    "TFR2-related_disorder|Hereditary_hemochromatosis": 2,
    "Inborn_genetic_diseases|Hereditary_hemochromatosis|TFR2-related_disorder|Hemochromatosis_type_3": 1,
    "Hemochromatosis_type_3|Hereditary_hemochromatosis|TFR2-related_disorder|not_provided": 1,
    "Hereditary_hemochromatosis|not_specified|not_provided|Hemochromatosis_type_3": 1,
    "not_provided|Hereditary_hemochromatosis|Hemochromatosis_type_3": 2,
    "Hemochromatosis_type_3|Inborn_genetic_diseases": 2,
    "TFR2-related_disorder|Hereditary_hemochromatosis|Hemochromatosis_type_3": 1,
    "Hemochromatosis_type_3|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_76|Intellectual_developmental_disorder_with_severe_speech_and_ambulation_defects": 1,
    "Developmental_and_epileptic_encephalopathy|_76|ACTL6B-related_recessive_epilepsy": 2,
    "ACTL6B-related_neurodevelopmental_disorder": 1,
    "ACTL6B-related_recessive_epilepsy|ACTL6B-related_BAFopathy|Developmental_and_epileptic_encephalopathy|_76": 1,
    "Developmental_and_epileptic_encephalopathy|_76": 25,
    "Intellectual_developmental_disorder_with_severe_speech_and_ambulation_defects|not_provided": 1,
    "ACTL6B-related_BAFopathy": 1,
    "ACTL6B-related_disorder": 10,
    "ACTL6B-related_recessive_epilepsy": 2,
    "Intellectual_developmental_disorder_with_severe_speech_and_ambulation_defects": 8,
    "Congenital_generalized_lipodystrophy_type_2": 12,
    "ACTL6B-related_recessive_epilepsy|Developmental_and_epileptic_encephalopathy|_76": 5,
    "ACTL6B-related_BAFopathy|Inborn_genetic_diseases|Intellectual_disability|ACTL6B-related_dominant_intellectual_disability|Autism|not_provided|Intellectual_developmental_disorder_with_severe_speech_and_ambulation_defects": 1,
    "Developmental_and_epileptic_encephalopathy|_76|Intellectual_disability|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_76": 1,
    "Developmental_and_epileptic_encephalopathy|_76|not_provided": 2,
    "ACTL6B-related_recessive_epilepsy|ACTL6B-related_disorder|Developmental_and_epileptic_encephalopathy|_76|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_76": 1,
    "ACTL6B-related_BAFopathy|not_provided|Developmental_and_epileptic_encephalopathy|_76|ACTL6B-related_recessive_epilepsy": 1,
    "not_provided|ACTL6B-related_disorder": 1,
    "not_provided|ACTL6B-related_recessive_epilepsy|Developmental_and_epileptic_encephalopathy|_76": 1,
    "ACTL6B-related_recessive_epilepsy|Developmental_and_epileptic_encephalopathy|_76|Intellectual_developmental_disorder_with_severe_speech_and_ambulation_defects": 1,
    "Autism|ACTL6B-related_dominant_intellectual_disability|Intellectual_developmental_disorder_with_severe_speech_and_ambulation_defects": 1,
    "Sick_sinus_syndrome_4": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_dysmorphic_facies": 6,
    "Neurodevelopmental_disorder_with_hypotonia_and_dysmorphic_facies|GNB2-related_disorder|not_provided": 1,
    "Global_developmental_delay|Neurodevelopmental_disorder_with_hypotonia_and_dysmorphic_facies": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "GNB2-related_disorder": 2,
    "GIGYF1-related_disorder": 34,
    "not_specified|GIGYF1-related_disorder": 1,
    "GIGYF1-related_disorder|not_provided": 4,
    "not_provided|GIGYF1-related_disorder": 4,
    "GIGYF1-associated_neurodevelopmental_disorder": 1,
    "Coffin-Siris_syndrome_6": 89,
    "GIGYF1-related_disorder|not_specified": 1,
    "GIGYF1-associated_disorder": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_2": 1,
    "EPO-related_disorder|not_provided": 2,
    "EPO-related_disorder": 7,
    "Erythrocytosis|_familial|_5": 2,
    "not_provided|EPO-related_disorder": 4,
    "not_specified|EPO-related_disorder": 1,
    "Diamond-Blackfan_anemia-like": 1,
    "EPHB4-related_disorder": 18,
    "EPHB4-related_disorder|Cardiovascular_phenotype": 4,
    "EPHB4-associated_vascular_malformation_spectrum": 3,
    "Lymphatic_malformation_7": 7,
    "Capillary_malformation-arteriovenous_malformation_2|not_provided": 13,
    "Capillary_malformation-arteriovenous_malformation_2": 40,
    "not_specified|Capillary_malformation-arteriovenous_malformation_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Lymphatic_malformation_7": 1,
    "Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2": 4,
    "not_specified|Capillary_malformation-arteriovenous_malformation_2": 1,
    "Lymphatic_malformation_7|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_2": 3,
    "EPHB4-related_disorder|not_provided": 4,
    "EPHB4-related_disorder|Capillary_malformation-arteriovenous_malformation_2|Cardiovascular_phenotype|not_provided": 1,
    "EPHB4-related_disorder|Capillary_malformation-arteriovenous_malformation_2|not_provided": 2,
    "Lymphatic_malformation_7|EPHB4-related_disorder": 1,
    "not_provided|EPHB4-related_disorder": 4,
    "Capillary_malformation-arteriovenous_malformation_2|not_provided|Cardiovascular_phenotype": 2,
    "EPHB4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|EPHB4-related_disorder|not_provided": 1,
    "Capillary_malformation-arteriovenous_malformation_2|Lymphatic_malformation_7": 2,
    "Cardiovascular_phenotype|EPHB4-related_disorder": 4,
    "Lymphatic_malformation_7|not_provided": 3,
    "Capillary_malformation-arteriovenous_malformation_2|Cardiovascular_phenotype": 2,
    "Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2|not_provided|Cardiovascular_phenotype": 3,
    "not_provided|Cardiovascular_phenotype|Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2": 1,
    "Capillary_malformation-arteriovenous_malformation_2|Lymphatic_malformation_7|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|EPHB4-related_disorder": 3,
    "Capillary_malformation-arteriovenous_malformation_2|Cardiovascular_phenotype|not_provided": 1,
    "Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2|Vein_of_Galen_aneurysmal_malformation": 1,
    "Cardiovascular_phenotype|not_provided|Venous_malformation": 1,
    "not_provided|Capillary_malformation-arteriovenous_malformation_2|Lymphatic_malformation_7|Cardiovascular_phenotype": 1,
    "Vein_of_Galen_aneurysmal_malformation": 8,
    "Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_2|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|EPHB4-related_disorder|Capillary_malformation-arteriovenous_malformation_2|Lymphatic_malformation_7": 1,
    "Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_2|Lymphatic_malformation_7|EPHB4-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Capillary_malformation-arteriovenous_malformation_2|EPHB4-related_disorder": 1,
    "not_provided|EPHB4-related_disorder|Cardiovascular_phenotype": 1,
    "Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2|Cardiovascular_phenotype": 1,
    "Lymphedema|Capillary_malformation-arteriovenous_malformation_2": 1,
    "EPHB4-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2|EPHB4-related_disorder": 1,
    "Capillary_malformation-arteriovenous_malformation_2|EPHB4-related_disorder": 1,
    "Cardiovascular_phenotype|Lymphatic_malformation_7|Capillary_malformation-arteriovenous_malformation_2": 1,
    "SRRT-related_condition": 1,
    "ACHE-related_disorder": 1,
    "not_provided|YT_BLOOD_GROUP_POLYMORPHISM": 1,
    "not_provided|ACHE-related_disorder": 1,
    "ACHE-related_disorder|not_provided": 1,
    "Congenital_plasminogen_activator_inhibitor_type_1_deficiency": 60,
    "SERPINE1-related_disorder|Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_an_impaired_coagulation_process|not_specified|not_provided|Congenital_plasminogen_activator_inhibitor_type_1_deficiency": 1,
    "Congenital_plasminogen_activator_inhibitor_type_1_deficiency|not_provided": 6,
    "SERPINE1-related_disorder": 2,
    "not_provided|Congenital_plasminogen_activator_inhibitor_type_1_deficiency": 10,
    "Congenital_plasminogen_activator_inhibitor_type_1_deficiency|SERPINE1-related_disorder": 2,
    "not_specified|Congenital_plasminogen_activator_inhibitor_type_1_deficiency": 2,
    "Gastrointestinal_hemorrhage|Hemorrhage": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|AP1S1-related_disorder": 1,
    "MEDNIK_syndrome|not_provided": 4,
    "not_provided|MEDNIK_syndrome": 3,
    "AP1S1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "MEDNIK_syndrome|not_provided|AP1S1-related_disorder": 1,
    "not_provided|AP1S1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|MEDNIK_syndrome": 1,
    "MEDNIK_syndrome": 1,
    "AP1S1-related_disorder|not_provided": 1,
    "Bone_fragility_with_contractures|_arterial_rupture|_and_deafness": 10,
    "PLOD3-related_disorder|not_provided": 11,
    "not_provided|PLOD3-related_disorder": 9,
    "not_provided|Bone_fragility_with_contractures|_arterial_rupture|_and_deafness": 8,
    "PLOD3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Bone_fragility_with_contractures|_arterial_rupture|_and_deafness|not_provided": 5,
    "Bone_fragility_with_contractures|_arterial_rupture|_and_deafness|not_provided|PLOD3-related_disorder": 1,
    "PLOD3-related_disorder": 4,
    "Bone_fragility_with_contractures|_arterial_rupture|_and_deafness|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|PLOD3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Bone_fragility_with_contractures|_arterial_rupture|_and_deafness": 1,
    "PLOD3-related_disorder|Bone_fragility_with_contractures|_arterial_rupture|_and_deafness|not_provided": 1,
    "not_provided|not_specified|PLOD3-related_disorder|Inborn_genetic_diseases": 1,
    "PLOD3-related_disorder|not_provided|Bone_fragility_with_contractures|_arterial_rupture|_and_deafness": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to": 8,
    "CUX1-related_disorder": 30,
    "Global_developmental_delay_with_or_without_impaired_intellectual_development": 88,
    "Global_developmental_delay_with_or_without_impaired_intellectual_development|Intellectual_disability": 1,
    "Global_developmental_delay_with_or_without_impaired_intellectual_development|not_provided": 11,
    "not_provided|CUX1-related_disorder": 8,
    "CUX1-related_disorder|not_provided": 3,
    "Neurodevelopmental_disorder|Global_developmental_delay_with_or_without_impaired_intellectual_development": 1,
    "Inborn_genetic_diseases|CUX1-related_disorder": 4,
    "Global_developmental_delay_with_or_without_impaired_intellectual_development|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Global_developmental_delay_with_or_without_impaired_intellectual_development": 3,
    "not_provided|Global_developmental_delay_with_or_without_impaired_intellectual_development": 4,
    "Myeloproliferative_neoplasm|Duane_retraction_syndrome": 1,
    "Inborn_genetic_diseases|Global_developmental_delay_with_or_without_impaired_intellectual_development|not_provided": 2,
    "PMPCB-related_disorder": 6,
    "PMPCB-related_disorder|Multiple_mitochondrial_dysfunctions_syndrome_6": 1,
    "not_provided|PMPCB-related_disorder|Inborn_genetic_diseases": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_6": 12,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_6|Inborn_genetic_diseases": 2,
    "Multiple_mitochondrial_dysfunctions_syndrome_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Multiple_mitochondrial_dysfunctions_syndrome_6": 2,
    "not_provided|PMPCB-related_disorder": 5,
    "PMPCB-related_disorder|not_provided": 3,
    "Multiple_mitochondrial_dysfunctions_syndrome_6|not_provided": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_6|PMPCB-related_mitochondrial_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Multiple_mitochondrial_dysfunctions_syndrome_6|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PMPCB-related_disorder": 1,
    "PMPCB-related_disorder|not_provided|Multiple_mitochondrial_dysfunctions_syndrome_6": 1,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_6": 2,
    "PMPCB-related_ataxia": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_6|Inborn_genetic_diseases|PMPCB-related_disorder|not_provided": 1,
    "not_provided|PMPCB-related_disorder|Multiple_mitochondrial_dysfunctions_syndrome_6|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_61": 7,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_61": 4,
    "not_provided|SLC26A5-related_disorder|Inborn_genetic_diseases": 1,
    "SLC26A5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|SLC26A5-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_61|Inborn_genetic_diseases": 1,
    "SLC26A5-related_disorder": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_61|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_61|not_provided": 1,
    "SLC26A5-related_disorder|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_61": 1,
    "SLC26A5-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_61|not_provided|not_specified": 1,
    "SLC26A5-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_61": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_61": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_61": 1,
    "Norman-Roberts_syndrome": 70,
    "Lissencephaly|_Recessive": 10,
    "Norman-Roberts_syndrome|not_provided": 9,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 979,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1416,
    "Inborn_genetic_diseases|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 35,
    "RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|not_provided": 7,
    "not_provided|not_specified|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 2,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1": 4,
    "Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided": 4,
    "Intellectual_disability|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 63,
    "Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 14,
    "RELN-related_disorder": 28,
    "Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided": 57,
    "not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 72,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 32,
    "not_specified|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 19,
    "Norman-Roberts_syndrome|not_specified|not_provided|Familial_temporal_lobe_epilepsy_7": 2,
    "RELN-related_disorder|not_provided": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified": 15,
    "not_specified|not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 5,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified": 19,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|not_specified": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided|not_specified": 8,
    "Inborn_genetic_diseases|not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 5,
    "Norman-Roberts_syndrome|not_specified|Familial_temporal_lobe_epilepsy_7": 3,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|RELN-related_disorder": 2,
    "not_specified|RELN-related_disorder|not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided": 39,
    "RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified|not_provided": 1,
    "Familial_temporal_lobe_epilepsy_7": 22,
    "RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 11,
    "Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|not_specified|not_provided": 4,
    "not_specified|not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 4,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified": 2,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases": 24,
    "not_provided|Inborn_genetic_diseases|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 4,
    "not_specified|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 20,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|not_specified|not_provided": 5,
    "not_provided|RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder|not_specified|not_provided": 2,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|RELN-related_disorder|not_specified|not_provided": 1,
    "RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified|not_provided": 7,
    "Familial_temporal_lobe_epilepsy_7|not_provided|Norman-Roberts_syndrome|Inborn_genetic_diseases|RELN-related_disorder|not_specified": 1,
    "Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder": 9,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Lissencephaly|_Recessive": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|See_cases|not_provided": 1,
    "Neurodevelopmental_delay|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided": 3,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1": 5,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified|not_provided": 15,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|not_specified|not_provided": 2,
    "not_specified|not_provided|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7": 1,
    "not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases": 3,
    "not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified": 4,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Generalized_epilepsy_with_febrile_seizures_plus|_type_2": 1,
    "RELN-related_disorder|not_specified|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided": 1,
    "not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder": 2,
    "Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7": 2,
    "RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided": 4,
    "Lissencephaly|not_provided": 1,
    "RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 4,
    "Inborn_genetic_diseases|not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 2,
    "not_specified|not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder": 1,
    "not_specified|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided|Epilepsy|_familial_temporal_lobe|_1": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided|Inborn_genetic_diseases": 5,
    "Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|not_provided": 4,
    "Familial_temporal_lobe_epilepsy_7|not_provided|Norman-Roberts_syndrome": 1,
    "not_specified|Norman-Roberts_syndrome|not_provided|Familial_temporal_lobe_epilepsy_7": 1,
    "not_provided|Norman-Roberts_syndrome|RELN-related_disorder|Familial_temporal_lobe_epilepsy_7": 1,
    "Familial_temporal_lobe_epilepsy_7|not_provided|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Sacroiliac_arthritis|Sacroiliac_joint_synovitis|Enthesitis|Kyphosis|Low_back_pain|Inflammation_of_the_large_intestine|Arthritis|Scoliosis|Synovitis": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided": 3,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified|RELN-related_disorder": 1,
    "not_specified|Norman-Roberts_syndrome|not_provided": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified|not_provided": 10,
    "Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided|not_specified": 3,
    "not_specified|Norman-Roberts_syndrome|not_provided|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|not_provided": 3,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder|Epilepsy|_familial_temporal_lobe|_1|not_specified|not_provided": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases|RELN-related_disorder|not_provided": 1,
    "not_specified|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases": 1,
    "See_cases|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|not_specified|not_provided|Intellectual_disability": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 2,
    "See_cases|Inborn_genetic_diseases|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 6,
    "not_provided|Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 2,
    "not_provided|RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 1,
    "RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided|not_specified": 1,
    "Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified|not_provided|RELN-related_disorder": 1,
    "Inborn_genetic_diseases|Epilepsy|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "RELN-related_disorder|not_specified|not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|Epilepsy|_familial_temporal_lobe|_1|not_provided": 1,
    "not_provided|Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 1,
    "not_specified|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|not_provided": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 2,
    "not_specified|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 2,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases": 2,
    "See_cases|not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|not_provided|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_provided|Lissencephaly|_Recessive|not_specified": 1,
    "not_provided|not_specified|Lissencephaly|_Recessive": 1,
    "not_provided|Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified": 1,
    "not_specified|RELN-related_disorder|not_provided": 1,
    "Lissencephaly|not_provided|not_specified|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|not_provided": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified|Lissencephaly|_Recessive": 1,
    "not_provided|not_specified|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder|not_specified": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified": 1,
    "not_provided|not_specified|RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Norman-Roberts_syndrome|not_specified": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified|not_provided": 2,
    "RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder|not_provided|not_specified|Intellectual_disability": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "RELN-related_disorder|not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases|not_specified": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_specified|RELN-related_disorder|not_provided": 1,
    "Norman-Roberts_syndrome|not_provided|Familial_temporal_lobe_epilepsy_7|not_specified": 1,
    "not_provided|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|RELN-related_disorder|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|RELN-related_disorder|not_specified|not_provided": 1,
    "not_provided|Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 2,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Self-limited_epilepsy_with_centrotemporal_spikes|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|RELN-related_disorder": 2,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder|not_provided": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases|RELN-related_disorder|not_provided": 1,
    "Norman-Roberts_syndrome|not_provided|RELN-related_disorder|Familial_temporal_lobe_epilepsy_7": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|not_provided|Seizure": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|RELN-related_disorder|not_provided": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|RELN-related_disorder|Inborn_genetic_diseases": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_provided|not_specified|Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1": 2,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Lissencephaly|_Recessive|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|not_specified|not_provided": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided|not_specified|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7": 1,
    "not_specified|not_provided|RELN-related_disorder|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Inborn_genetic_diseases|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|not_provided": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|RELN-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "RELN-related_disorder|not_provided|not_specified|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Inborn_genetic_diseases|RELN-related_disorder|not_specified|not_provided": 1,
    "Norman-Roberts_syndrome|not_provided|Familial_temporal_lobe_epilepsy_7": 1,
    "Norman-Roberts_syndrome|not_provided|RELN-related_disorder|not_specified|Familial_temporal_lobe_epilepsy_7": 1,
    "RELN-related_disorder|not_specified|Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|not_provided": 1,
    "not_specified|Norman-Roberts_syndrome": 1,
    "Norman-Roberts_syndrome|Inborn_genetic_diseases": 1,
    "Norman-Roberts_syndrome|Familial_temporal_lobe_epilepsy_7|Epilepsy|_familial_temporal_lobe|_1|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Epilepsy|_familial_temporal_lobe|_1|not_specified": 1,
    "RELN-related_disorder|Lissencephaly|_Recessive|not_provided": 1,
    "Familial_temporal_lobe_epilepsy_7|Norman-Roberts_syndrome|Lissencephaly|_Recessive|not_provided|not_specified": 1,
    "not_specified|RELN-related_disorder|not_provided|Lissencephaly|_Recessive": 1,
    "not_provided|RELN-related_disorder|not_specified|Lissencephaly|_Recessive": 1,
    "Lissencephaly|_Recessive|not_provided": 4,
    "not_specified|Lissencephaly|_Recessive|RELN-related_disorder": 1,
    "RELN-related_disorder|Lissencephaly|_Recessive": 1,
    "RELN-related_disorder|not_provided|Lissencephaly|_Recessive": 1,
    "O'Donnell-Luria-Rodan_syndrome": 97,
    "KMT2E-related_disorder|not_provided": 18,
    "not_provided|O'Donnell-Luria-Rodan_syndrome": 8,
    "not_provided|KMT2E-related_disorder": 14,
    "KMT2E-related_disorder": 25,
    "O'Donnell-Luria-Rodan_syndrome|not_provided": 10,
    "O'Donnell-Luria-Rodan_syndrome|See_cases|not_provided": 1,
    "not_provided|O'Donnell-Luria-Rodan_syndrome|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_40|not_provided": 1,
    "Abnormal_cerebellar_vermis_morphology|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|O'Donnell-Luria-Rodan_syndrome": 2,
    "KMT2E-related_disorder|not_specified": 2,
    "O'Donnell-Luria-Rodan_syndrome|not_provided|See_cases|Inborn_genetic_diseases": 1,
    "KMT2E-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "O'Donnell-Luria-Rodan_syndrome|Intellectual_disability": 1,
    "O'Donnell-Luria-Rodan_syndrome|Neurodevelopmental_disorder": 1,
    "not_provided|See_cases|O'Donnell-Luria-Rodan_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|KMT2E-related_disorder": 2,
    "See_cases|O'Donnell-Luria-Rodan_syndrome": 4,
    "Global_developmental_delay|O'Donnell-Luria-Rodan_syndrome|not_provided": 1,
    "KMT2E-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "O'Donnell-Luria-Rodan_syndrome|Inborn_genetic_diseases": 1,
    "O'Donnell-Luria-Rodan_syndrome|See_cases": 1,
    "Inborn_genetic_diseases|KMT2E-related_disorder|not_provided": 1,
    "not_provided|KMT2E-related_disorder|Inborn_genetic_diseases": 1,
    "O'Donnell-Luria-Rodan_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 81,
    "O'Donnell-Luria-Rodan_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|KMT2E-related_disorder|O'Donnell-Luria-Rodan_syndrome|Inborn_genetic_diseases": 1,
    "SRPK2-related_disorder": 5,
    "SRPK2-related_disorder|not_provided": 2,
    "not_provided|SRPK2-related_disorder": 1,
    "PUS7-related_disorder": 9,
    "Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature": 32,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature": 3,
    "Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature|not_provided": 1,
    "PUS7-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature": 1,
    "Pervasive_developmental_disorder|Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature": 1,
    "not_provided|Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature": 4,
    "not_provided|PUS7-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_abnormal_behavior|_microcephaly|_and_short_stature|Inborn_genetic_diseases": 1,
    "Infantile_liver_failure_syndrome_3|not_provided|not_specified": 1,
    "not_provided|RINT1-related_disorder|not_specified": 4,
    "not_specified|RINT1-related_disorder|Infantile_liver_failure_syndrome_3|not_provided": 1,
    "not_provided|Infantile_liver_failure_syndrome_3|not_specified": 2,
    "not_specified|not_provided|Infantile_liver_failure_syndrome_3": 4,
    "RINT1-related_disorder|not_provided|not_specified": 3,
    "Infantile_liver_failure_syndrome_3|not_specified|not_provided": 7,
    "RINT1-related_disorder|not_specified|not_provided": 3,
    "Infantile_liver_failure_syndrome_3": 8,
    "not_specified|not_provided|RINT1-related_disorder": 2,
    "not_provided|Infantile_liver_failure_syndrome_3": 3,
    "Thyroid_cancer|_nonmedullary|_1|not_specified|not_provided": 1,
    "Infantile_liver_failure_syndrome_3|not_provided": 2,
    "Thyroid_cancer|_nonmedullary|_1|not_provided": 1,
    "Fulminant_hepatic_failure|Infantile_liver_failure_syndrome_3": 1,
    "not_specified|Infantile_liver_failure_syndrome_3|not_provided": 2,
    "Infantile_liver_failure_syndrome_3|not_specified": 1,
    "Familial_ovarian_cancer|not_provided|Fulminant_hepatic_failure|not_specified|Infantile_liver_failure_syndrome_3": 1,
    "not_provided|not_specified|Infantile_liver_failure_syndrome_3": 1,
    "not_specified|Infantile_liver_failure_syndrome_3": 1,
    "not_specified|not_provided|RINT1-related_disorder|Infantile_liver_failure_syndrome_3": 1,
    "RINT1-related_disorder": 1,
    "RINT1-related_disorder|not_specified": 1,
    "Familial_ovarian_cancer|not_specified|not_provided": 1,
    "RINT1-related_disorder|not_specified|not_provided|Infantile_liver_failure_syndrome_3": 1,
    "RINT1-related_disorder|not_provided": 1,
    "not_specified|Susceptibility_to_nonsyndromic_otitis_media": 1,
    "Susceptibility_to_nonsyndromic_otitis_media|not_provided": 2,
    "not_provided|Susceptibility_to_nonsyndromic_otitis_media": 1,
    "not_specified|Susceptibility_to_nonsyndromic_otitis_media|not_provided": 1,
    "Immunodeficiency_97_with_autoinflammation": 5,
    "not_provided|Cystic_fibrosis": 90,
    "Immunodeficiency_97_with_autoinflammation|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cystic_fibrosis": 1,
    "Immunodeficiency_97_with_autoinflammation|not_specified": 1,
    "PIK3CG-related_disorder": 1,
    "COG5-congenital_disorder_of_glycosylation": 629,
    "COG5-congenital_disorder_of_glycosylation|not_provided": 14,
    "not_provided|COG5-congenital_disorder_of_glycosylation": 21,
    "COG5-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 13,
    "not_specified|COG5-congenital_disorder_of_glycosylation": 6,
    "not_specified|COG5-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|COG5-congenital_disorder_of_glycosylation": 30,
    "Congenital_disorder_of_glycosylation|COG5-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Craniosynostosis_syndrome|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-related_disorder|COG5-congenital_disorder_of_glycosylation": 4,
    "COG5-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|COG5-congenital_disorder_of_glycosylation": 1,
    "not_provided|COG5-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-congenital_disorder_of_glycosylation|not_specified": 6,
    "not_provided|not_specified|COG5-congenital_disorder_of_glycosylation": 2,
    "COG5-related_disorder|COG5-congenital_disorder_of_glycosylation|not_specified": 1,
    "COG5-related_disorder|not_specified|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-congenital_disorder_of_glycosylation|not_specified|not_provided|COG5-related_disorder": 1,
    "not_provided|not_specified|COG5-related_disorder|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-congenital_disorder_of_glycosylation|COG5-related_disorder": 6,
    "SLC26A4-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|COG5-congenital_disorder_of_glycosylation": 2,
    "COG5-related_disorder|not_provided|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-related_disorder|not_provided|not_specified|COG5-congenital_disorder_of_glycosylation": 3,
    "not_specified|not_provided|COG5-congenital_disorder_of_glycosylation": 5,
    "COG5-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|COG5-related_disorder": 2,
    "COG5-related_disorder|Inborn_genetic_diseases|not_provided|COG5-congenital_disorder_of_glycosylation": 1,
    "not_specified|COG5-congenital_disorder_of_glycosylation|COG5-related_disorder|not_provided": 1,
    "COG5-related_disorder|COG5-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "not_provided|COG5-congenital_disorder_of_glycosylation|not_specified": 1,
    "COG5-related_disorder": 3,
    "Inborn_genetic_diseases|COG5-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_specified|COG5-congenital_disorder_of_glycosylation|not_provided": 2,
    "not_provided|COG5-related_disorder|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-related_disorder|COG5-congenital_disorder_of_glycosylation|not_provided": 1,
    "Inborn_genetic_diseases|COG5-related_disorder|COG5-congenital_disorder_of_glycosylation": 1,
    "COG5-congenital_disorder_of_glycosylation|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|COG5-congenital_disorder_of_glycosylation|COG5-related_disorder": 2,
    "not_specified|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 13,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|Hearing_impairment": 1,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|not_specified": 2,
    "not_specified|not_provided|SLC26A4-related_disorder": 1,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 40,
    "not_specified|SLC26A4-related_disorder|Rare_genetic_deafness|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided": 1,
    "Rare_genetic_deafness|SLC26A4-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 2,
    "Pendred_syndrome|not_provided": 30,
    "not_provided|Pendred_syndrome": 31,
    "not_specified|Pendred_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 3,
    "SLC26A4-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "Rare_genetic_deafness|not_provided|Pendred_syndrome": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|Monogenic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided|Wolff-Parkinson-White_pattern|Ear_malformation": 1,
    "not_provided|Rare_genetic_deafness|Pendred_syndrome": 2,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 25,
    "SLC26A4-related_disorder|not_specified|not_provided": 1,
    "Pendred_syndrome|SLC26A4-related_disorder|not_provided": 1,
    "Rare_genetic_deafness|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 8,
    "not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Rare_genetic_deafness": 2,
    "not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 26,
    "not_specified|SLC26A4-related_disorder|Pendred_syndrome|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|Hearing_impairment|Pendred_syndrome|SLC26A4-related_disorder": 1,
    "Pendred_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 10,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_specified": 4,
    "SLC26A4-related_disorder|not_provided": 4,
    "not_provided|not_specified|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 2,
    "Hearing_loss|_autosomal_recessive|not_provided|Pendred_syndrome|Deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Pendred_syndrome": 14,
    "RASopathy|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Rare_genetic_deafness|SLC26A4-related_disorder|not_specified|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 2,
    "Pendred_syndrome|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Pendred_syndrome|Hearing_impairment|Rare_genetic_deafness|not_provided|SLC26A4-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|not_specified|Pendred_syndrome": 1,
    "Pendred_syndrome|not_provided|not_specified": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|Pendred_syndrome|not_provided": 1,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|not_provided": 5,
    "SLC26A4-related_disorder|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Pendred_syndrome|Monogenic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided|not_specified": 2,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_impairment|not_specified": 1,
    "not_specified|Pendred_syndrome|not_provided": 5,
    "Pendred_syndrome|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_specified|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 3,
    "SLC26A4-related_disorder|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 3,
    "Pendred_syndrome|not_specified|not_provided": 3,
    "not_specified|not_provided|Pendred_syndrome": 2,
    "not_specified|Pendred_syndrome": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Sensorineural_hearing_loss_disorder": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|Hearing_impairment|Ear_malformation": 1,
    "Rare_genetic_deafness|SLC26A4-related_disorder|Deafness|not_specified|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided|Hearing_impairment": 1,
    "Rare_genetic_deafness|Deafness|Sensorineural_hearing_loss_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "Pendred_syndrome|not_specified|not_provided|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "SLC26A4-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "not_provided|SLC26A4-related_disorder|not_specified|Pendred_syndrome": 1,
    "Ear_malformation|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "SLC26A4-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|Rare_genetic_deafness|not_provided": 1,
    "Rare_genetic_deafness|SLC26A4-related_disorder|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Ear_malformation": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|SLC26A4-related_disorder|not_provided|Pendred_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Pendred_syndrome|Rare_genetic_deafness|not_provided|SLC26A4-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Pendred_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Pendred_syndrome|not_specified": 3,
    "SLC26A4-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|Pendred_syndrome|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|SLC26A4-related_disorder": 1,
    "not_specified|Hearing_impairment": 3,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Rare_genetic_deafness|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Rare_genetic_deafness|SLC26A4-related_disorder|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 2,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Rare_genetic_deafness|Monogenic_hearing_loss|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Pendred_syndrome|Rare_genetic_deafness": 2,
    "Rare_genetic_deafness|not_provided|not_specified|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_loss|_autosomal_recessive|Ear_malformation": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Pendred_syndrome|SLC26A4-related_disorder": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Pendred_syndrome": 1,
    "Rare_genetic_deafness|SLC26A4-related_disorder|Inborn_genetic_diseases|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Pendred_syndrome": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_specified|not_provided": 2,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|See_cases": 1,
    "Pendred_syndrome|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 3,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "not_specified|Microcephaly_5|_primary|_autosomal_recessive|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified|not_provided|Pendred_syndrome": 1,
    "not_provided|Rare_genetic_deafness|Deafness|Hearing_impairment|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Rare_genetic_deafness": 1,
    "Pendred_syndrome|Rare_genetic_deafness": 1,
    "not_provided|Pendred_syndrome|not_specified": 3,
    "Pendred_syndrome|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided|Rare_genetic_deafness": 1,
    "not_specified|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|SLC26A4-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|SLC26A4-related_disorder": 1,
    "SLC26A4-related_disorder|not_provided|not_specified|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "SLC26A4-related_disorder|not_specified|Hearing_impairment|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome": 1,
    "Inborn_genetic_diseases|Pendred_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|Pendred_syndrome|not_specified": 1,
    "SLC26A4-related_disorder|not_specified|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "Deafness|Rare_genetic_deafness|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|SLC26A4-related_disorder|Pendred_syndrome": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_impairment": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|Hearing_loss|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|SLC26A4-related_disorder|Pendred_syndrome|not_specified": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|Pendred_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "SLC26A4-related_disorder|Rare_genetic_deafness|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_specified|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Pendred_syndrome|not_provided|SLC26A4-related_disorder": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_4|Pendred_syndrome|Hearing_impairment": 1,
    "Rare_genetic_deafness|Pendred_syndrome|not_provided": 2,
    "Rare_genetic_deafness|Hearing_impairment|Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided": 1,
    "Pendred_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_4|Inborn_genetic_diseases|not_provided": 1,
    "Hearing_loss|Pendred_syndrome|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_4": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Pendred_syndrome": 1,
    "Hearing_loss|_autosomal_recessive|Pendred_syndrome": 1,
    "Pendred_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "Congenital_secretory_diarrhea|_chloride_type": 79,
    "not_provided|Congenital_secretory_diarrhea|_chloride_type": 39,
    "not_provided|Congenital_secretory_diarrhea|_chloride_type|SLC26A3-related_disorder": 3,
    "Gastrointestinal_obstruction|Hydrops_fetalis|Polyhydramnios": 1,
    "not_specified|not_provided|Congenital_secretory_diarrhea|_chloride_type": 1,
    "SLC26A3-related_disorder|not_provided": 4,
    "Congenital_secretory_diarrhea|_chloride_type|not_provided": 18,
    "not_provided|Congenital_secretory_diarrhea|_chloride_type|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Congenital_secretory_diarrhea|_chloride_type": 2,
    "not_provided|SLC26A3-related_disorder": 4,
    "SLC26A3-related_disorder": 2,
    "Congenital_secretory_diarrhea|_chloride_type|not_provided|SLC26A3-related_disorder": 1,
    "Congenital_secretory_diarrhea|_chloride_type|SLC26A3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "SLC26A3-related_disorder|not_provided|Congenital_secretory_diarrhea|_chloride_type": 3,
    "Intestinal_obstruction|Hydrops_fetalis|Polyhydramnios": 1,
    "Congenital_secretory_diarrhea|_chloride_type|SLC26A3-related_disorder|not_provided": 1,
    "not_specified|Congenital_secretory_diarrhea|_chloride_type": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_secretory_diarrhea|_chloride_type": 1,
    "SLC26A3-related_disorder|Congenital_secretory_diarrhea|_chloride_type|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_secretory_diarrhea|_chloride_type": 1,
    "Intestinal_obstruction|Hydrops_fetalis|Polyhydramnios|not_provided|Congenital_secretory_diarrhea|_chloride_type": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|Pyruvate_dehydrogenase_complex_deficiency|Leigh_syndrome": 15,
    "Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency": 19,
    "Pyruvate_dehydrogenase_E3_deficiency": 495,
    "not_specified|not_provided|Pyruvate_dehydrogenase_E3_deficiency|Pyruvate_dehydrogenase_complex_deficiency|Leigh_syndrome": 2,
    "Pyruvate_dehydrogenase_E3_deficiency|not_provided": 5,
    "Pyruvate_dehydrogenase_E3_deficiency|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Leigh_syndrome": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|Inborn_genetic_diseases": 1,
    "DLD-related_disorder": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Pyruvate_dehydrogenase_E3_deficiency": 12,
    "not_specified|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome": 2,
    "not_specified|Pyruvate_dehydrogenase_E3_deficiency": 6,
    "DLD-related_disorder|Pyruvate_dehydrogenase_E3_deficiency": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|not_specified": 2,
    "Pyruvate_dehydrogenase_E3_deficiency|DLD-related_disorder": 2,
    "Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E3_deficiency|not_provided|not_specified|Leigh_syndrome": 1,
    "Maple_syrup_urine_disease|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome": 2,
    "Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome": 4,
    "Pyruvate_dehydrogenase_E3_deficiency|Pyruvate_dehydrogenase_complex_deficiency|not_provided|Leigh_syndrome|not_specified": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E3_deficiency": 3,
    "Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E3_deficiency": 3,
    "not_specified|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Leigh_syndrome|Pyruvate_dehydrogenase_E3_deficiency": 1,
    "DLD-related_disorder|not_provided|Pyruvate_dehydrogenase_E3_deficiency": 2,
    "not_provided|not_specified|Pyruvate_dehydrogenase_E3_deficiency": 2,
    "Pyruvate_dehydrogenase_complex_deficiency|not_specified|not_provided|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome": 2,
    "not_specified|Pyruvate_dehydrogenase_E3_deficiency|Pyruvate_dehydrogenase_complex_deficiency|Leigh_syndrome|not_provided": 1,
    "DLD-related_disorder|Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E3_deficiency": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|not_provided|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "DLD-related_disorder|Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome": 1,
    "not_provided|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|See_cases|DLD-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Leigh_syndrome|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E3_deficiency|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "Pyruvate_dehydrogenase_E3_deficiency|Lactic_acidosis": 1,
    "not_provided|Pyruvate_dehydrogenase_E3_deficiency|DLD-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E3_deficiency": 1,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E3_deficiency|not_provided": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|not_provided|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|not_specified": 1,
    "not_provided|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency": 4,
    "Pyruvate_dehydrogenase_E3_deficiency|Pyruvate_dehydrogenase_complex_deficiency|not_provided|Leigh_syndrome": 4,
    "Pyruvate_dehydrogenase_complex_deficiency|not_provided|Pyruvate_dehydrogenase_E3_deficiency|Leigh_syndrome": 2,
    "Maple_syrup_urine_disease|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|not_provided": 6,
    "LAMB1-related_disorder": 12,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|not_provided|not_specified|Maple_syrup_urine_disease|Leigh_syndrome|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "Classic_lissencephaly": 1,
    "Inborn_genetic_diseases|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|not_provided": 2,
    "LAMB1-related_disorder|not_provided": 14,
    "not_provided|LAMB1-related_disorder": 11,
    "not_specified|not_provided|LAMB1-related_disorder": 2,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement": 29,
    "LAMB1-related_disorder|not_specified|not_provided": 5,
    "not_provided|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|Inborn_genetic_diseases": 2,
    "not_provided|LAMB1-related_disorder|not_specified": 1,
    "not_provided|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|LAMB1-related_disorder": 1,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|LAMB1-related_disorder": 1,
    "LAMB1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement": 1,
    "LAMB1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement": 1,
    "LAMB1-related_disorder|not_provided|not_specified": 5,
    "LAMB1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|Inborn_genetic_diseases": 2,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|Intellectual_disability": 1,
    "not_provided|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement": 2,
    "LAMB1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement": 1,
    "not_specified|LAMB1-related_disorder|not_provided": 1,
    "not_specified|Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|not_provided": 1,
    "Cobblestone_lissencephaly_without_muscular_or_ocular_involvement|Inborn_genetic_diseases|not_provided": 1,
    "Multiple_sclerosis|LAMB1-related_disorder|not_provided|not_specified": 1,
    "not_provided|NRCAM-related_disorder": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_neuromuscular_and_skeletal_abnormalities": 1,
    "Neurodevelopmental_disorder_with_neuromuscular_and_skeletal_abnormalities": 12,
    "NRCAM-related_disorder": 14,
    "NRCAM-related_disorder|Neurodevelopmental_disorder_with_neuromuscular_and_skeletal_abnormalities": 3,
    "Neurodevelopmental_disorder_with_neuromuscular_and_skeletal_abnormalities|NRCAM-related_disorder|Inborn_genetic_diseases": 1,
    "NRCAM-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|NRCAM-related_disorder": 3,
    "Neurodevelopmental_disorder_with_neuromuscular_and_skeletal_abnormalities|NRCAM-related_disorder": 2,
    "Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome|not_provided|not_specified": 1,
    "Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome": 19,
    "Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome|Inborn_genetic_diseases": 2,
    "PNPLA8-related_disorder|not_provided": 2,
    "not_provided|Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome": 4,
    "PNPLA8-related_disorder": 5,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome": 1,
    "PNPLA8-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PNPLA8-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome|not_provided": 3,
    "PNPLA8-related_disorder|Mitochondrial_myopathy-lactic_acidosis-deafness_syndrome|not_provided": 1,
    "IMMP2L-related_disorder": 2,
    "DOCK4-related_disorder": 11,
    "DOCK4-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|IFRD1-related_disorder": 1,
    "IFRD1-related_disorder": 1,
    "GLYCEMIA_VARIATION": 1,
    "PPP1R3A-related_disorder|not_provided|Insulin_resistance|_susceptibility_to|Type_2_diabetes_mellitus": 1,
    "not_provided|PPP1R3A-related_disorder|Type_2_diabetes_mellitus": 2,
    "Monogenic_diabetes|PPP1R3A-related_disorder": 1,
    "PPP1R3A-related_disorder": 1,
    "INSULIN_RESISTANCE|_SEVERE|_DIGENIC|DIABETES_MELLITUS|_TYPE_II|_DIGENIC|Monogenic_diabetes|not_specified|not_provided": 1,
    "PPP1R3A-related_disorder|Monogenic_diabetes|not_provided": 1,
    "Monogenic_diabetes|not_provided|PPP1R3A-related_disorder": 2,
    "PPP1R3A-related_disorder|not_provided|Type_2_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|not_specified": 2,
    "not_provided|Childhood_apraxia_of_speech": 16,
    "Inborn_genetic_diseases|FOXP2-related_disorder|not_provided|Childhood_apraxia_of_speech": 1,
    "Childhood_apraxia_of_speech|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Childhood_apraxia_of_speech": 4,
    "FOXP2-related_disorder|Inborn_genetic_diseases": 3,
    "FOXP2-related_disorder": 13,
    "FOXP2-related_disorder|Childhood_apraxia_of_speech|not_provided": 1,
    "not_provided|FOXP2-related_disorder": 1,
    "Inborn_genetic_diseases|FOXP2-related_disorder|not_provided|not_specified|Childhood_apraxia_of_speech": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Childhood_apraxia_of_speech": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Childhood_apraxia_of_speech": 1,
    "FOXP2-related_disorder|not_specified|not_provided|Childhood_apraxia_of_speech|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Childhood_apraxia_of_speech": 1,
    "Childhood_apraxia_of_speech|FOXP2-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Childhood_apraxia_of_speech|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|Childhood_apraxia_of_speech|See_cases": 1,
    "Inborn_genetic_diseases|Childhood_apraxia_of_speech|not_provided": 2,
    "not_provided|Childhood_apraxia_of_speech|Inborn_genetic_diseases": 2,
    "FOXP2-related_disorder|not_specified|Childhood_apraxia_of_speech|not_provided": 1,
    "FOXP2-related_disorder|Childhood_apraxia_of_speech": 1,
    "Inborn_genetic_diseases|Childhood_apraxia_of_speech|not_specified": 1,
    "Inborn_genetic_diseases|FOXP2-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|Childhood_apraxia_of_speech": 1,
    "MDFIC-related_disorder": 1,
    "Lymphatic_malformation_12": 4,
    "MDFIC-related_disorder|Lymphatic_malformation_12": 1,
    "CAV1-related_disorder": 3,
    "Pulmonary_hypertension|_primary|_3": 33,
    "Inborn_genetic_diseases|not_provided|Pulmonary_hypertension|_primary|_3": 1,
    "Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Pulmonary_hypertension|_primary|_3": 15,
    "not_provided|Pulmonary_hypertension|_primary|_3|not_specified": 2,
    "not_provided|Pulmonary_hypertension|_primary|_3": 1,
    "Pulmonary_hypertension|_primary|_3|not_provided|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3": 1,
    "Pulmonary_hypertension|_primary|_3|Congenital_generalized_lipodystrophy_type_3|not_provided|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome": 1,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_3": 2,
    "Pulmonary_hypertension|_primary|_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome": 1,
    "Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3|Pulmonary_hypertension|_primary|_3|Inborn_genetic_diseases|not_provided": 1,
    "Pulmonary_hypertension|_primary|_3|Inborn_genetic_diseases": 12,
    "Inborn_genetic_diseases|not_provided|Pulmonary_hypertension|_primary|_3|not_specified": 1,
    "Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Pulmonary_hypertension|_primary|_3|Inborn_genetic_diseases": 1,
    "Pulmonary_hypertension|_primary|_3|Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy_type_3": 1,
    "Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Pulmonary_hypertension|_primary|_3|Congenital_generalized_lipodystrophy_type_3": 1,
    "Pulmonary_hypertension|_primary|_3|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease": 1,
    "not_provided|Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_3|Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome": 1,
    "Pulmonary_hypertension|_primary|_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|not_provided": 1,
    "Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2|CAV1-related_disorder|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Pulmonary_hypertension|_primary|_3|Congenital_generalized_lipodystrophy_type_3": 1,
    "Pulmonary_hypertension|_primary|_3|Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome": 1,
    "Pulmonary_hypertension|_primary|_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome": 1,
    "Inborn_genetic_diseases|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3|Pulmonary_hypertension|_primary|_3|not_provided": 1,
    "Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3|Pulmonary_hypertension|_primary|_3|Inborn_genetic_diseases": 1,
    "Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome": 4,
    "Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Pulmonary_hypertension|_primary|_3|not_provided": 1,
    "Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3": 1,
    "Pulmonary_hypertension|_primary|_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3": 1,
    "Pulmonary_hypertension|_primary|_3|not_provided|CAV1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3|Pulmonary_hypertension|_primary|_3": 1,
    "Congenital_generalized_lipodystrophy_type_3|Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Pulmonary_hypertension|_primary|_3|not_provided|Monogenic_diabetes": 1,
    "Partial_lipodystrophy|_congenital_cataracts|_and_neurodegeneration_syndrome|Congenital_generalized_lipodystrophy_type_3|Pulmonary_hypertension|_primary|_3": 1,
    "Pulmonary_hypertension|_primary|_3|Inborn_genetic_diseases|CAV1-related_disorder": 1,
    "Autism|_susceptibility_to|_9": 1,
    "not_provided|Renal_cell_carcinoma": 10,
    "Papillary_renal_cell_carcinoma_type_1|not_provided": 2,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|not_specified": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1|not_provided": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 484,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 361,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 77,
    "MET-related_disorder|not_specified|Renal_cell_carcinoma|not_provided|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 11,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided": 7,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 67,
    "not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 20,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 25,
    "not_provided|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 9,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|MET-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|not_provided": 2,
    "MET-related_disorder|Papillary_renal_cell_carcinoma_type_1|not_provided|Lymphedema|not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_provided": 28,
    "Renal_cell_carcinoma|not_provided": 20,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 50,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 55,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_provided": 1,
    "Hereditary_cancer|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Renal_cell_carcinoma|not_specified|Osteofibrous_dysplasia|not_provided": 1,
    "MET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 11,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 34,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 40,
    "Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 34,
    "Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided|MET-related_disorder|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Intellectual_disability": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|MET-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 8,
    "Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 21,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 11,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97": 15,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 16,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Hereditary_papillary_renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_specified": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Renal_cell_carcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_specified|not_provided": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 65,
    "Renal_cell_carcinoma|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 17,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 3,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma": 37,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 30,
    "Renal_cell_carcinoma|not_provided|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_specified": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_specified": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hereditary_papillary_renal_cell_carcinoma": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma": 1,
    "Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast_carcinoma": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Renal_cell_carcinoma|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Renal_cell_carcinoma": 1,
    "Hereditary_cancer|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "Renal_cell_carcinoma|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|not_specified|Papillary_renal_cell_carcinoma_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Osteofibrous_dysplasia": 3,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Intellectual_disability|not_specified|not_provided|Renal_cell_carcinoma": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma": 5,
    "Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer": 1,
    "not_provided|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Lymphedema": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 3,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Renal_cell_carcinoma": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Papillary_renal_cell_carcinoma_type_1": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder|Renal_cell_carcinoma": 2,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Renal_cell_carcinoma": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 3,
    "MET-related_disorder|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Papillary_renal_cell_carcinoma_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|not_specified": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 9,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 2,
    "Hereditary_papillary_renal_cell_carcinoma|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 2,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11": 1,
    "Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Papillary_renal_cell_carcinoma_type_1|Intellectual_disability|Renal_cell_carcinoma": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|MET-related_disorder|Renal_cell_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_specified|Renal_cell_carcinoma": 2,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 4,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Papillary_renal_cell_carcinoma_type_1": 1,
    "MET-related_disorder|Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 6,
    "Papillary_renal_cell_carcinoma_type_1|MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|not_specified|Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Hereditary_cancer-predisposing_syndrome|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_provided": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Papillary_renal_cell_carcinoma_type_1": 5,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Papillary_renal_cell_carcinoma_type_1|not_provided|Renal_cell_carcinoma": 1,
    "Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_papillary_renal_cell_carcinoma|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Renal_cell_carcinoma|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "MET-related_disorder|Papillary_renal_cell_carcinoma_type_1|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "MET-related_disorder": 4,
    "Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma": 5,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_provided": 2,
    "Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|not_provided|MET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_specified|not_provided": 1,
    "Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|MET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Renal_cell_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Arthrogryposis|_distal|_IIa_11|MET-related_disorder|Renal_cell_carcinoma": 1,
    "not_provided|Renal_cell_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Renal_cell_carcinoma": 4,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "MET-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Renal_cell_carcinoma|not_specified": 7,
    "not_specified|not_provided|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Renal_cell_carcinoma|not_specified|Lymphedema": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|MET-related_disorder|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 2,
    "Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|MET-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_provided": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_provided": 3,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_provided|MET-related_disorder": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Osteofibrous_dysplasia|not_provided": 1,
    "MET-related_disorder|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma|not_provided": 1,
    "not_specified|Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|MET-related_disorder|not_provided": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_specified|not_provided": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hepatoblastoma|not_specified|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Renal_cell_carcinoma|MET-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "MET-related_disorder|not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Squamous_cell_lung_carcinoma|Breast_carcinoma|MET-related_disorder|not_provided|not_specified|Renal_cell_carcinoma": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Papillary_renal_cell_carcinoma_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 2,
    "not_provided|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "Nonsyndromic_genetic_hearing_loss|not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Ovarian_cancer|Renal_cell_carcinoma": 1,
    "not_specified|Renal_cell_carcinoma": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|MET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Arthrogryposis|_distal|_IIa_11|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia": 1,
    "not_specified|not_provided|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "not_specified|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_provided|Ovarian_cancer|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hereditary_cancer|Papillary_renal_cell_carcinoma_type_1": 1,
    "MET-related_disorder|Renal_cell_carcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_provided|Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 3,
    "not_provided|MET-related_disorder|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 1,
    "not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Renal_cell_carcinoma": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Hereditary_cancer|Osteofibrous_dysplasia|Renal_cell_carcinoma|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|MET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|MET-related_disorder": 1,
    "Renal_cell_carcinoma|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Nonsyndromic_Hearing_Loss_and_Deafness|_Autosomal_Recessive": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_papillary_renal_cell_carcinoma|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided": 1,
    "not_provided|Renal_cell_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_papillary_renal_cell_carcinoma|Renal_cell_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Renal_cell_carcinoma|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma|not_provided": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_provided|not_specified|Renal_cell_carcinoma": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_provided": 1,
    "MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|MET-related_disorder|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Ovarian_cancer": 1,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|not_specified|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|MET-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|MET-related_disorder|not_provided|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11|Papillary_renal_cell_carcinoma_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Osteofibrous_dysplasia|not_provided|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Classic_Hodgkin_lymphoma|Congenital_diaphragmatic_hernia": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_papillary_renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Intellectual_disability|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Renal_cell_carcinoma": 2,
    "Renal_cell_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_provided|MET-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Arthrogryposis|_distal|_IIa_11": 1,
    "Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Renal_cell_carcinoma|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 2,
    "Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|MET-related_disorder": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_papillary_renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 2,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|not_specified": 1,
    "Renal_cell_carcinoma|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 1,
    "Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|MET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Renal_cell_carcinoma": 1,
    "Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|MET-related_disorder": 1,
    "Pediatric_hepatocellular_carcinoma": 3,
    "not_provided|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Renal_cell_carcinoma": 1,
    "not_specified|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|not_specified|not_provided": 1,
    "Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|MET-related_disorder|Renal_cell_carcinoma": 1,
    "not_specified|not_provided|Renal_cell_carcinoma": 1,
    "MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|not_provided": 1,
    "Arthrogryposis|_distal|_type_1A|Arthrogryposis|_distal|_IIa_11": 1,
    "MET-related_disorder|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|not_specified|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Osteofibrous_dysplasia": 1,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_specified|Papillary_renal_cell_carcinoma_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MET-related_disorder|not_provided|Renal_cell_carcinoma": 1,
    "Papillary_renal_cell_carcinoma_type_1|MET-related_disorder|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma|not_provided": 1,
    "not_provided|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Arthrogryposis|_distal|_IIa_11|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|not_specified|Renal_cell_carcinoma": 1,
    "Arthrogryposis|_distal|_IIa_11|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_papillary_renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|not_provided|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Renal_cell_carcinoma|MET-related_disorder|Papillary_renal_cell_carcinoma_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hereditary_cancer-predisposing_syndrome|not_specified|Papillary_renal_cell_carcinoma_type_1|not_provided": 1,
    "not_provided|MET-related_disorder|Renal_cell_carcinoma|Osteofibrous_dysplasia|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Papillary_renal_cell_carcinoma_type_1": 1,
    "Papillary_renal_cell_carcinoma_type_1|not_provided|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_97": 1,
    "Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_cell_carcinoma|not_provided|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Renal_cell_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Papillary_renal_cell_carcinoma_type_1|Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_97|Papillary_renal_cell_carcinoma_type_1|Hepatocellular_carcinoma|Osteofibrous_dysplasia|Hereditary_cancer-predisposing_syndrome|Renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|MET-related_disorder|Renal_cell_carcinoma|Papillary_renal_cell_carcinoma_type_1": 1,
    "Renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Papillary_renal_cell_carcinoma_type_1": 1,
    "not_specified|Renal_cell_carcinoma|not_provided|Osteofibrous_dysplasia|Hepatocellular_carcinoma|Papillary_renal_cell_carcinoma_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_97|Arthrogryposis|_distal|_IIa_11|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hepatocellular_carcinoma|Autosomal_recessive_nonsyndromic_hearing_loss_97|Osteofibrous_dysplasia|Papillary_renal_cell_carcinoma_type_1|Arthrogryposis|_distal|_IIa_11|Renal_cell_carcinoma": 1,
    "Global_developmental_delay|Brain_atrophy|Intractable_seizure": 1,
    "ST7-related_disorder": 4,
    "ST7-related_disorder|not_provided": 1,
    "not_specified|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "CFTR-related_disorder": 297,
    "Cystic_fibrosis|not_provided": 86,
    "not_provided|Hereditary_pancreatitis|Cystic_fibrosis": 2,
    "Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 5,
    "not_specified|Cystic_fibrosis|not_provided": 13,
    "Cystic_fibrosis|CFTR-related_disorder": 153,
    "CFTR-related_disorder|not_provided|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "not_specified|not_provided|Cystic_fibrosis": 21,
    "not_provided|Hereditary_pancreatitis|not_specified|Cystic_fibrosis": 1,
    "CFTR-related_disorder|not_provided": 5,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis": 21,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis": 26,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 6,
    "CFTR-related_disorder|not_provided|not_specified|Hereditary_pancreatitis|Cystic_fibrosis": 3,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis": 32,
    "not_provided|CFTR-related_disorder|Cystic_fibrosis": 8,
    "Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_provided": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 48,
    "not_specified|CFTR-related_disorder|Cystic_fibrosis": 20,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 27,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 7,
    "Cystic_fibrosis|not_specified": 124,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided": 14,
    "CFTR-related_disorder|Cystic_fibrosis|not_specified|not_provided": 3,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_provided|not_specified": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 3,
    "not_provided|Cystic_fibrosis|not_specified|CFTR-related_disorder": 2,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis": 5,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder": 3,
    "not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "CFTR-related_disorder|Cystic_fibrosis": 137,
    "not_provided|Cystic_fibrosis|CFTR-related_disorder": 19,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder|not_provided": 1,
    "not_specified|Cystic_fibrosis|CFTR-related_disorder": 12,
    "Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 12,
    "CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis": 1,
    "not_specified|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_provided|CFTR-related_disorder": 1,
    "not_provided|Lung_disease|_non-specific|not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_provided|not_specified|Cystic_fibrosis": 11,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 12,
    "CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 2,
    "not_specified|Cystic_fibrosis": 122,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided": 16,
    "CFTR-related_disorder|not_specified|not_provided|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "not_specified|CFTR-related_disorder|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "not_specified|CFTR-related_disorder": 10,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Cystic_fibrosis|not_specified": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 2,
    "not_specified|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 1,
    "not_specified|not_provided|Hereditary_pancreatitis|Cystic_fibrosis": 5,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 2,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|ivacaftor_response_-_Efficacy|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|not_provided": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder|Cystic_fibrosis|not_provided": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 12,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|CFTR-related_disorder": 5,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 4,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 29,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|ivacaftor_response_-_Efficacy": 2,
    "CFTR-related_disorder|Cystic_fibrosis|not_specified": 13,
    "CFTR-related_disorder|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|ivacaftor_response_-_Efficacy": 1,
    "Abnormality_of_the_pancreas|CFTR-related_disorder|not_specified|not_provided|Hereditary_pancreatitis|Cystic_fibrosis|Lung_disease|_non-specific": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 4,
    "not_provided|CFTR-related_disorder|Cystic_fibrosis|not_specified": 7,
    "Cystic_fibrosis|not_specified|not_provided": 11,
    "Cystic_fibrosis|not_provided|CFTR-related_disorder": 3,
    "CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 2,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified": 14,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis": 6,
    "CFTR-related_disorder|Cystic_fibrosis|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder|Cystic_fibrosis": 6,
    "CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|not_specified": 1,
    "Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 10,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|not_specified": 1,
    "CFTR-related_disorder|not_specified|not_provided|Hereditary_pancreatitis|Cystic_fibrosis": 10,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|CFTR-related_disorder|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified|Cystic_fibrosis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 3,
    "CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 5,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 7,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy|not_provided": 1,
    "not_specified|not_provided|Cystic_fibrosis|CFTR-related_disorder": 6,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|See_cases|not_provided": 1,
    "not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy": 3,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Pseudomonas_aeruginosa|_susceptibility_to_chronic_infection_by|_in_cystic_fibrosis|Obstructive_azoospermia|ivacaftor_response_-_Efficacy": 1,
    "Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 3,
    "not_provided|not_specified|Cystic_fibrosis|CFTR-related_disorder": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|not_provided": 8,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_specified|not_provided|Infertility_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "not_specified|CFTR-related_disorder|not_provided|Cystic_fibrosis": 3,
    "Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 7,
    "not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Cystic_fibrosis": 7,
    "not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 2,
    "CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 2,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Cystic_fibrosis": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Cystic_fibrosis|not_specified|CFTR-related_disorder|not_provided": 1,
    "not_provided|Cystic_fibrosis|CFTR-related_disorder|not_specified": 7,
    "Cystic_fibrosis|not_provided|CFTR-related_disorder|Spermatogenic_failure|_Y-linked|_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 1,
    "Cystic_fibrosis|not_specified|not_provided|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_provided|Hereditary_pancreatitis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|CFTR-related_disorder|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 5,
    "not_provided|CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 5,
    "Cystic_fibrosis|not_specified|CFTR-related_disorder": 15,
    "CFTR-related_disorder|Chronic_pancreatitis|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_specified|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis|not_provided|CFTR-related_disorder|not_specified": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Obstructive_azoospermia|not_provided": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 7,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 4,
    "not_specified|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|not_specified": 1,
    "not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 3,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|ivacaftor_response_-_Efficacy": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|Cystic_fibrosis|CFTR-related_disorder": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|not_specified": 1,
    "Hereditary_pancreatitis|not_provided|Cystic_fibrosis": 3,
    "CFTR-related_disorder|not_provided|not_specified|Nephronophthisis_14|Cystic_fibrosis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 2,
    "not_provided|Cystic_fibrosis|not_specified": 8,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|not_specified|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_provided|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_specified": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|not_specified": 3,
    "not_provided|not_specified|CFTR-related_disorder|Cystic_fibrosis": 4,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Cystic_fibrosis": 2,
    "not_specified|CFTR-related_disorder|not_provided": 1,
    "Cystic_fibrosis|Hereditary_pancreatitis": 3,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified|not_provided|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified|not_provided": 5,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_provided|CFTR-related_disorder": 1,
    "not_provided|CFTR-related_disorder|not_specified|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified|not_provided": 2,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis": 3,
    "not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|CFTR-related_disorder": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_specified|not_provided|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "Cystic_fibrosis|not_specified|not_provided|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|not_provided|not_specified|CFTR-related_disorder": 4,
    "Cystic_fibrosis|not_provided|not_specified": 11,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Obstructive_azoospermia|Cystic_fibrosis": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder|Cystic_fibrosis": 1,
    "Cystic_fibrosis|not_provided|CFTR-related_disorder|not_specified": 3,
    "CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis|not_provided": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Inborn_genetic_diseases|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "not_provided|CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified|Hereditary_pancreatitis|not_provided": 1,
    "not_specified|not_provided|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "not_provided|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_provided|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_provided|Hereditary_pancreatitis|Cystic_fibrosis|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder|not_provided|Hereditary_pancreatitis": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|not_provided|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_provided|not_specified|Cystic_fibrosis": 12,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_provided|ivacaftor_response_-_Efficacy|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis": 1,
    "not_specified|Cystic_fibrosis|Hereditary_pancreatitis": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_provided": 2,
    "not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|CFTR-related_disorder": 2,
    "CFTR-related_disorder|not_specified|not_provided|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Hereditary_pancreatitis|Cystic_fibrosis": 4,
    "not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "Cystic_fibrosis|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 3,
    "not_specified|not_provided|Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Cystic_fibrosis": 1,
    "not_provided|CFTR-related_disorder|Cystic_fibrosis|Inborn_genetic_diseases|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_specified": 1,
    "not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|_modifier_of|Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_absence_of_vas_deferens|not_specified|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Obstructive_azoospermia": 1,
    "CFTR-related_disorder|not_specified": 6,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Hereditary_pancreatitis": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 2,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Cystic_fibrosis|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|CFTR-related_disorder": 1,
    "Hereditary_pancreatitis|Cystic_fibrosis|not_specified|not_provided": 1,
    "Cystic_fibrosis|not_specified|not_provided|CFTR-related_disorder": 5,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_pancreatitis": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_provided|not_specified": 1,
    "not_specified|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder|not_provided": 1,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|not_specified|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|not_specified": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 5,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 3,
    "not_specified|Hereditary_pancreatitis|CFTR-related_disorder|not_provided|Cystic_fibrosis": 2,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Obstructive_azoospermia": 1,
    "CFTR-related_disorder|not_provided|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "CFTR-related_disorder|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 2,
    "not_specified|Cystic_fibrosis|not_provided|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 3,
    "not_provided|not_specified|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "Cystic_fibrosis|not_provided|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 3,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 1,
    "CFTR-related_disorder|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|_modifier_of|Recurrent_pancreatitis|Obstructive_azoospermia|Duodenal_stenosis|ivacaftor_/_lumacaftor_response_-_Efficacy|ivacaftor_/_tezacaftor_response_-_Efficacy|See_cases": 1,
    "CFTR-related_disorder|not_provided|not_specified|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Infertility_disorder|Obstructive_azoospermia": 1,
    "Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Abnormality_of_metabolism/homeostasis": 1,
    "not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder": 1,
    "CFTR-related_disorder|not_specified|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 2,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|CFTR-related_disorder|not_specified": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|not_specified": 1,
    "Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder|not_specified|not_provided": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|Pancreatitis|not_specified|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "not_provided|CFTR-related_disorder": 8,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|CFTR-related_disorder|not_provided": 1,
    "not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|not_specified": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Hereditary_pancreatitis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|ivacaftor_response_-_Efficacy": 2,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Hereditary_pancreatitis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 2,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis": 1,
    "Cystic_fibrosis|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_specified|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 2,
    "CFTR-related_disorder|not_specified|not_provided": 2,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_provided|Hereditary_pancreatitis|CFTR-related_disorder|not_specified|Cystic_fibrosis": 1,
    "not_specified|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis|not_provided": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Cystic_fibrosis|not_specified": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Hereditary_pancreatitis": 1,
    "not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|not_provided|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Chronic_sinusitis|Lung_disease|_non-specific": 1,
    "not_specified|not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy": 1,
    "not_provided|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis": 2,
    "Hereditary_pancreatitis|Cystic_fibrosis|not_specified": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|not_specified|CFTR-related_disorder": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|CFTR-related_disorder|not_provided": 1,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 2,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_provided": 1,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|not_provided": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|CFTR-related_disorder|Cystic_fibrosis": 1,
    "Cystic_fibrosis|not_provided|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "Hereditary_pancreatitis|CFTR-related_disorder|Cystic_fibrosis|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder|not_specified": 2,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|not_specified": 1,
    "CFTR-related_disorder|not_specified|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Chronic_sinusitis|Lung_disease|_non-specific": 1,
    "CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 2,
    "not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder|not_provided|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|See_cases": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis": 2,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 2,
    "not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_specified|not_provided|CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "CFTR-related_disorder|not_specified|Obstructive_azoospermia|not_provided|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Hereditary_pancreatitis|Cystic_fibrosis|not_provided|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "not_provided|CFTR-related_disorder|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "not_specified|CFTR-related_disorder|Cystic_fibrosis|not_provided": 3,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis|not_specified|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|CFTR-related_disorder": 1,
    "Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|CFTR-related_disorder|Fetal_cystic_hygroma": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified": 1,
    "not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder": 1,
    "CFTR-related_disorder|not_specified|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "Hereditary_pancreatitis|not_specified|CFTR-related_disorder|Cystic_fibrosis|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Obstructive_azoospermia|not_specified": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|CFTR-related_disorder": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|Hereditary_pancreatitis": 1,
    "not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|CFTR-related_disorder": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|CFTR-related_disorder": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Hereditary_pancreatitis|not_specified|CFTR-related_disorder|Cystic_fibrosis": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|not_specified": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified|not_provided|Breast_neoplasm|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_specified|Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 2,
    "CFTR-related_disorder|not_provided|not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|not_provided|not_specified|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "not_specified|not_provided|Cystic_fibrosis|Obstructive_azoospermia": 1,
    "not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder|not_specified": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_provided": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 2,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|not_specified|Cystic_fibrosis": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 2,
    "CFTR-related_disorder|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 3,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|ivacaftor_response_-_Efficacy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Chronic_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Infertility_disorder": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 3,
    "Obstructive_azoospermia": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_provided|Hereditary_pancreatitis|ivacaftor_response_-_Efficacy|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|not_provided": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 2,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_specified": 3,
    "CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|Pancreatitis|not_specified|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|Infertility_disorder|.|.|Obstructive_azoospermia": 1,
    "CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Obstructive_azoospermia": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 2,
    "not_provided|Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided": 1,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Congenital_bilateral_absence_of_vas_deferens|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy|Hereditary_pancreatitis|not_provided": 1,
    "CFTR-related_disorder|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|ivacaftor_response_-_Efficacy|Obstructive_azoospermia": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 1,
    "Cystic_fibrosis|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_specified|not_provided|CFTR-related_disorder|Cystic_fibrosis": 2,
    "not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|CFTR-related_disorder": 1,
    "not_specified|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_provided|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|not_provided": 1,
    "not_provided|Cystic_fibrosis|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 1,
    "not_specified|not_provided|Infertility_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis": 1,
    "CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "Cystic_fibrosis|Pseudomonas_aeruginosa|_susceptibility_to_chronic_infection_by|_in_cystic_fibrosis": 1,
    "not_specified|Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder|not_provided": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|ivacaftor_response_-_Efficacy|not_provided|Hereditary_pancreatitis|Cystic_fibrosis|Male_infertility|Obstructive_azoospermia|CFTR-related_disorder": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "not_specified|Cystic_fibrosis|CFTR-related_disorder|not_provided": 2,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_specified": 1,
    "not_provided|not_specified|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis": 1,
    "CFTR-related_disorder|not_specified|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "not_specified|not_provided|Cystic_fibrosis|CFTR-related_disorder|Obstructive_azoospermia|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis": 2,
    "Cystic_fibrosis|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|not_specified": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|not_specified|not_provided": 1,
    "CFTR-related_disorder|not_specified|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis|Obstructive_azoospermia": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|CFTR-related_disorder|not_provided": 2,
    "not_specified|Cystic_fibrosis|CFTR-related_disorder|Hereditary_pancreatitis|not_provided": 1,
    "Hereditary_pancreatitis|Cystic_fibrosis|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Cystic_fibrosis|not_specified|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|Hereditary_pancreatitis|Cystic_fibrosis": 2,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|ivacaftor_response_-_Efficacy": 1,
    "Hereditary_pancreatitis|Cystic_fibrosis|ivacaftor_response_-_Efficacy": 1,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|not_provided|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "CFTR-related_disorder|not_provided|not_specified|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "ivacaftor_response_-_Efficacy|Cystic_fibrosis": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_specified|not_provided|Hereditary_pancreatitis": 1,
    "Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Hereditary_pancreatitis|CFTR-related_disorder|not_provided|not_specified": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|not_provided|CFTR-related_disorder": 1,
    "Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Hereditary_pancreatitis": 1,
    "not_provided|Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|not_provided|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Spermatogenic_failure|_Y-linked|_2": 1,
    "Cystic_fibrosis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided|not_specified": 1,
    "Cystic_fibrosis|Hereditary_pancreatitis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|CFTR-related_disorder|not_specified": 1,
    "Hereditary_pancreatitis|CFTR-related_disorder|ivacaftor_response_-_Efficacy|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "not_provided|Hereditary_pancreatitis|Cystic_fibrosis|CFTR-related_disorder|not_specified": 1,
    "Cystic_fibrosis|CFTR-related_disorder|not_provided|not_specified|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_provided|Cystic_fibrosis|not_specified": 3,
    "CFTR-related_disorder|not_specified|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "not_provided|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|CFTR-related_disorder": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "CFTR-related_disorder|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Hereditary_pancreatitis|not_specified|Cystic_fibrosis|not_provided": 1,
    "CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Cystic_fibrosis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis": 1,
    "CFTR-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Hereditary_pancreatitis|Cystic_fibrosis": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|CFTR-related_disorder|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Sweat_chloride_elevation_without_cystic_fibrosis|not_provided": 1,
    "CFTR-related_disorder|not_specified|not_provided|Cystic_fibrosis|Hereditary_pancreatitis": 1,
    "Cystic_fibrosis|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Hereditary_pancreatitis|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "CTTNBP2-related_disorder|not_provided": 3,
    "CTTNBP2-related_disorder": 28,
    "CTTNBP2-related_disorder|not_specified": 1,
    "Early_myoclonic_encephalopathy": 1493,
    "Early_myoclonic_encephalopathy|Inborn_genetic_diseases": 12,
    "not_provided|Early_myoclonic_encephalopathy": 29,
    "Inborn_genetic_diseases|Early_myoclonic_encephalopathy": 3,
    "Early_myoclonic_encephalopathy|not_specified": 84,
    "Early_myoclonic_encephalopathy|not_provided": 51,
    "not_specified|not_provided|KCND2-related_disorder|Early_myoclonic_encephalopathy": 1,
    "Early_myoclonic_encephalopathy|Inborn_genetic_diseases|not_specified": 1,
    "Early_myoclonic_encephalopathy|Neurodevelopmental_disorder": 1,
    "not_specified|not_provided|Early_myoclonic_encephalopathy": 2,
    "Early_myoclonic_encephalopathy|not_specified|KCND2-related_disorder|Inborn_genetic_diseases": 1,
    "KCND2-related_disorder|Early_myoclonic_encephalopathy": 1,
    "KCND2-related_neurodevelopmental_disorder": 1,
    "not_specified|Early_myoclonic_encephalopathy|not_provided": 2,
    "Early_myoclonic_encephalopathy|KCND2-related_disorder": 1,
    "Early_myoclonic_encephalopathy|KCND2-related_neurodevelopmental_disorder|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Early_myoclonic_encephalopathy": 1,
    "Early_myoclonic_encephalopathy|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Early_myoclonic_encephalopathy": 55,
    "Inborn_genetic_diseases|not_specified|Early_myoclonic_encephalopathy": 1,
    "not_provided|not_specified|KCND2-related_disorder|Early_myoclonic_encephalopathy": 1,
    "Early_myoclonic_encephalopathy|not_provided|not_specified": 1,
    "KCND2-related_disorder": 1,
    "KCND2-associated_neurodevelopmental_syndrome": 1,
    "Exudative_vitreoretinopathy_5": 39,
    "Familial_exudative_vitreoretinopathy": 12,
    "Exudative_vitreoretinopathy_5|not_provided": 12,
    "TSPAN12-related_disorder|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_5": 10,
    "Exudative_vitreoretinopathy_5|not_specified|not_provided": 1,
    "Persistent_hyperplastic_primary_vitreous|_autosomal_recessive|Exudative_vitreoretinopathy_5|Atrophia_bulborum_hereditaria|Familial_exudative_vitreoretinopathy|not_provided": 1,
    "not_provided|TSPAN12-related_disorder": 2,
    "not_provided|not_specified|Familial_exudative_vitreoretinopathy": 1,
    "not_provided|Exudative_vitreoretinopathy_5|TSPAN12-related_disorder": 1,
    "Familial_exudative_vitreoretinopathy|TSPAN12-related_disorder": 1,
    "not_provided|TSPAN12-related_disorder|Inborn_genetic_diseases": 1,
    "Vitreoretinopathy": 3,
    "Inborn_genetic_diseases|Exudative_vitreoretinopathy_5": 1,
    "Familial_exudative_vitreoretinopathy|not_provided": 7,
    "not_provided|Familial_exudative_vitreoretinopathy": 3,
    "Hyperlysinemia|Saccharopinuria|not_specified|not_provided": 1,
    "Hyperlysinemia": 16,
    "Hyperlysinemia|not_provided": 1,
    "not_provided|Hyperlysinemia": 4,
    "Hyperlysinemia|Saccharopinuria": 1,
    "AASS-related_disorder|not_provided": 2,
    "not_provided|AASS-related_disorder|Hyperlysinemia": 1,
    "Inborn_genetic_diseases|Hyperlysinemia": 1,
    "Hyperlysinemia|Saccharopinuria|not_provided": 1,
    "AASS-related_disorder": 1,
    "not_provided|FEZF1-related_disorder|not_specified": 2,
    "Amenorrhea|not_provided": 1,
    "not_provided|FEZF1-related_disorder": 3,
    "FEZF1-related_disorder|not_provided": 3,
    "Hypogonadotropic_hypogonadism_22_with_anosmia": 2,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_22_with_or_without_anosmia|not_provided": 1,
    "FEZF1-related_disorder": 1,
    "FEZF1-related_disorder|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_22_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "CADPS2-related_disorder|not_provided": 1,
    "CADPS2-related_disorder": 6,
    "TAS2R16-related_disorder": 2,
    "BETA-GLUCOPYRANOSIDE_TASTING|Alcohol_dependence|Alcohol_dependence|_susceptibility_to": 1,
    "Cardiomyopathy|_dilated|_2G": 7,
    "Cardiomyopathy|_dilated|_2G|Familial_isolated_dilated_cardiomyopathy": 1,
    "Inborn_genetic_diseases|LMOD2-related_condition": 1,
    "LMOD2-related_condition": 1,
    "Tumor_predisposition_syndrome_3": 812,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3": 276,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 345,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 32,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 28,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|not_provided": 18,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3": 1,
    "Tumor_predisposition_syndrome_3|not_provided|Hereditary_cancer-predisposing_syndrome": 23,
    "not_specified|not_provided|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tumor_predisposition_syndrome_3": 22,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|POT1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|not_specified": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3": 15,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3": 3,
    "Tumor_predisposition_syndrome_3|not_provided": 17,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Tumor_predisposition_syndrome_3|POT1-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified": 8,
    "Tumor_predisposition_syndrome_3|POT1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Tumor_predisposition_syndrome_3|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 3,
    "POT1-related_disorder|Tumor_predisposition_syndrome_3": 1,
    "Tumor_predisposition_syndrome_3|not_specified": 4,
    "not_specified|Tumor_predisposition_syndrome_3": 7,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Tumor_predisposition_syndrome_3": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Glioma_susceptibility_1|Tumor_predisposition_syndrome_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tumor_predisposition_syndrome_3|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|not_provided|Tumor_predisposition_syndrome_3": 2,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tumor_predisposition_syndrome_3|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|not_provided": 1,
    "POT1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3": 1,
    "Long_telomere_syndrome|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|POT1-related_disorder|Tumor_predisposition_syndrome_3": 4,
    "not_provided|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3": 1,
    "not_specified|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tumor_predisposition_syndrome_3": 7,
    "Tumor_predisposition_syndrome_3|Melanoma|_cutaneous_malignant|_susceptibility_to|_9": 1,
    "not_provided|Tumor_predisposition_syndrome_3": 12,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|POT1-related_disorder": 1,
    "Tumor_predisposition_syndrome_3|POT1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hoyeraal-Hreidarsson_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Tumor_predisposition_syndrome_3|Inherited_aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Hereditary_cancer-predisposing_syndrome|POT1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tumor_predisposition_syndrome_3": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|POT1-related_disorder": 1,
    "Tumor_predisposition_syndrome_3|Long_telomere_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Tumor_predisposition_syndrome_3|not_provided": 3,
    "POT1-related_disorder|Tumor_predisposition_syndrome_3|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Tumor_predisposition_syndrome_3|not_provided|Hereditary_cancer|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tumor_predisposition_syndrome_3|Polycystic_kidney_disease_4": 1,
    "Hereditary_cancer-predisposing_syndrome|POT1-related_disorder|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Tumor_predisposition_syndrome_3": 1,
    "Long_telomere_syndrome|Tumor_predisposition_syndrome_3": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|POT1-related_disorder|not_provided": 1,
    "POT1-related_disorder|not_provided|Tumor_predisposition_syndrome_3": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8": 1,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|POT1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3": 1,
    "POT1-related_disorder": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "POT1-related_disorder|not_provided|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|not_provided": 1,
    "Tumor_predisposition_syndrome_3|High-grade_astrocytoma_with_piloid_features": 1,
    "Hereditary_cancer-predisposing_syndrome|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|not_specified|not_provided|POT1-related_disorder": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tumor_predisposition_syndrome_3": 2,
    "not_provided|POT1-related_disorder|Tumor_predisposition_syndrome_3|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Long_telomere_syndrome|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tumor_predisposition_syndrome_3|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3|POT1-related_disorder": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|POT1-related_disorder|Tumor_predisposition_syndrome_3": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|POT1-related_disorder|Tumor_predisposition_syndrome_3": 1,
    "Tumor_predisposition_syndrome_3|Breast_carcinoma": 1,
    "Familial_melanoma|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|Dyskeratosis_congenita": 1,
    "Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POT1-related_disorder|Tumor_predisposition_syndrome_3": 1,
    "Tumor_predisposition_syndrome_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Long_telomere_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Long_telomere_syndrome|Tumor_predisposition_syndrome_3|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "Long_telomere_syndrome|Tumor_predisposition_syndrome_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Long_telomere_syndrome|Tumor_predisposition_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Tumor_predisposition_syndrome_3": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|POT1-related_disorder|Tumor_predisposition_syndrome_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_8|Tumor_predisposition_syndrome_3|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_provided|Tumor_predisposition_syndrome_3": 1,
    "Tumor_predisposition_syndrome_3|not_specified|not_provided": 1,
    "GRM8-related_disorder": 5,
    "not_specified|not_provided|GRM8-related_disorder": 1,
    "GRM8-related_disorder|not_provided": 3,
    "not_provided|GRM8-related_disorder": 3,
    "not_provided|PAX4-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus": 1,
    "PAX4-related_disorder": 8,
    "PAX4-related_disorder|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|not_provided": 2,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Type_2_diabetes_mellitus": 3,
    "PAX4-related_disorder|Monogenic_diabetes|Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_9|not_provided|not_specified": 1,
    "PAX4-related_disorder|not_provided|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus": 3,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_9|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_ketosis-prone|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|not_provided|PAX4-related_disorder": 1,
    "Diabetes_mellitus|_ketosis-prone|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|not_specified|not_provided|PAX4-related_disorder": 1,
    "Diabetes_mellitus|_ketosis-prone|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus": 3,
    "Diabetes_mellitus|_ketosis-prone|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|not_specified": 1,
    "Diabetes_mellitus|_ketosis-prone|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|not_provided": 4,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_9": 2,
    "not_specified|Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_9|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 3,
    "not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_9|Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_9|not_provided": 3,
    "PAX4-related_disorder|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_9": 1,
    "Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|Diabetes_mellitus|_ketosis-prone|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_9|not_provided|PAX4-related_disorder": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided|Diabetes_mellitus|_ketosis-prone|_susceptibility_to|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_specified|not_provided|PAX4-related_disorder": 1,
    "not_provided|PAX4-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_9|Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_9|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus|not_specified|not_provided|PAX4-related_disorder": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_9|not_specified|not_provided|Diabetes_mellitus|_ketosis-prone|_susceptibility_to|Hyperglycemia": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_9|Diabetes_mellitus|_ketosis-prone|Type_2_diabetes_mellitus": 1,
    "not_specified|PAX4-related_disorder": 1,
    "not_provided|PAX4-related_disorder": 1,
    "not_provided|Diabetes_mellitus|_ketosis-prone|Maturity-onset_diabetes_of_the_young_type_9|Type_2_diabetes_mellitus": 1,
    "SND1-related_disorder": 3,
    "not_provided|Monogenic_Non-Syndromic_Obesity|Obesity_due_to_congenital_leptin_deficiency": 5,
    "LEP-related_disorder": 23,
    "Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_congenital_leptin_deficiency|LEP-related_disorder": 1,
    "not_provided|LEP-related_disorder": 4,
    "Obesity_due_to_congenital_leptin_deficiency|LEP-related_disorder|not_provided": 1,
    "LEP-related_disorder|Obesity_due_to_congenital_leptin_deficiency": 1,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_congenital_leptin_deficiency": 16,
    "not_provided|Obesity_due_to_congenital_leptin_deficiency": 1,
    "Leptin_dysfunction|Obesity_due_to_congenital_leptin_deficiency": 1,
    "Obesity_due_to_congenital_leptin_deficiency|Leptin_dysfunction": 1,
    "not_provided|LEP-related_disorder|not_specified": 1,
    "not_provided|Monogenic_Non-Syndromic_Obesity|Monogenic_diabetes|Obesity_due_to_congenital_leptin_deficiency": 1,
    "Leptin_dysfunction": 1,
    "LEP-related_disorder|not_provided": 4,
    "Obesity_due_to_congenital_leptin_deficiency|not_provided": 1,
    "Obesity_due_to_congenital_leptin_deficiency|Monogenic_Non-Syndromic_Obesity|not_provided": 3,
    "Obesity_due_to_congenital_leptin_deficiency|Monogenic_Non-Syndromic_Obesity": 14,
    "Monogenic_Non-Syndromic_Obesity|Obesity_due_to_congenital_leptin_deficiency|not_provided": 2,
    "Monogenic_Non-Syndromic_Obesity|not_provided|Obesity_due_to_congenital_leptin_deficiency": 1,
    "ANE_syndrome": 7,
    "not_provided|RBM28-related_disorder": 2,
    "RBM28-related_disorder|not_provided": 3,
    "RBM28-related_disorder": 4,
    "ANE_syndrome|not_specified": 1,
    "Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_11": 27,
    "not_provided|Leber_congenital_amaurosis_11|Retinitis_pigmentosa": 7,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_11": 13,
    "Leber_congenital_amaurosis_11|Retinitis_pigmentosa": 9,
    "not_provided|Retinitis_pigmentosa_10|Leber_congenital_amaurosis_11": 2,
    "IMPDH1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_10": 8,
    "Leber_congenital_amaurosis_11|Retinitis_pigmentosa_10|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_specified|not_provided|Leber_congenital_amaurosis_11": 1,
    "Retinitis_pigmentosa_10|not_provided": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_11": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_11|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Leber_congenital_amaurosis_11": 2,
    "not_provided|Leber_congenital_amaurosis_11": 1,
    "not_provided|IMPDH1-related_disorder|Retinal_dystrophy|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_10|Retinal_dystrophy": 3,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_10|Leber_congenital_amaurosis_11": 1,
    "IMPDH1-related_disorder|not_provided": 4,
    "not_provided|Leber_congenital_amaurosis_11|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|IMPDH1-related_disorder": 4,
    "not_provided|Retinitis_pigmentosa_10|Leber_congenital_amaurosis_11|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_11": 1,
    "Leber_congenital_amaurosis_11|not_specified|not_provided|Retinitis_pigmentosa_10|IMPDH1-related_disorder|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_10": 1,
    "Retinitis_pigmentosa_10|Leber_congenital_amaurosis_11|not_provided|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_11|not_provided": 1,
    "Leber_congenital_amaurosis_11": 3,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_10": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_11": 1,
    "not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_11|Retinal_dystrophy|not_specified": 1,
    "Retinitis_pigmentosa_10|Retinal_dystrophy": 1,
    "not_specified|Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases|IMPDH1-related_disorder|Leber_congenital_amaurosis_11": 1,
    "Retinitis_pigmentosa|not_provided|Inborn_genetic_diseases|Leber_congenital_amaurosis_11": 1,
    "not_provided|Retinitis_pigmentosa_10|IMPDH1-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_11": 1,
    "Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_11": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Leber_congenital_amaurosis_11|Retinitis_pigmentosa_10": 1,
    "Leber_congenital_amaurosis_11|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_10|Leber_congenital_amaurosis_11": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_11|not_provided|IMPDH1-related_disorder": 1,
    "not_provided|OPN1SW-related_disorder": 2,
    "OPN1SW-related_disorder|not_provided|not_specified": 1,
    "Blue_color_blindness|not_provided": 1,
    "OPN1SW-related_disorder|not_provided": 5,
    "not_provided|Blue_color_blindness": 3,
    "not_provided|Blue_color_blindness|OPN1SW-related_disorder": 1,
    "not_specified|not_provided|Blue_color_blindness": 1,
    "not_provided|FLNC-related_disorder|not_specified": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 245,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 629,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 209,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 7,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 90,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 17,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 19,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 28,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 197,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 69,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 9,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 106,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 101,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 21,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 16,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 15,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 4,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 79,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 35,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 6,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 10,
    "FLNC-related_disorder": 11,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 32,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 37,
    "Hypertrophic_cardiomyopathy_26": 55,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 27,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 4,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided": 6,
    "not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 3,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 23,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 99,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 191,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided": 3,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 15,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 32,
    "Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 77,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 16,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 62,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 11,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 69,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 9,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 243,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype": 15,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 5,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 4,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 17,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 9,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided": 3,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 11,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided": 2,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 48,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided": 9,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided": 14,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 40,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 6,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 4,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 13,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 17,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 8,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 13,
    "Primary_dilated_cardiomyopathy|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 9,
    "Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 2,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 5,
    "not_specified|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 1,
    "Cardiovascular_phenotype|FLNC-related_disorder|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 54,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 13,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 59,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 110,
    "not_specified|FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|not_specified|FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype": 10,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 17,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype": 4,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 4,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 3,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 15,
    "Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 2,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 8,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 17,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Desmin-related_myofibrillar_myopathy|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 12,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 9,
    "not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 3,
    "Cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 2,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 10,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|not_specified": 1,
    "not_specified|not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided": 3,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 16,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 7,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 7,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 15,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 7,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 23,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 4,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_specified|not_provided": 6,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 9,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 3,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided": 5,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 6,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 19,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 11,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiovascular_phenotype": 4,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 23,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 4,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 2,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 7,
    "FLNC-related_disorder|Arrhythmogenic_cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 2,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 12,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 1,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Cardiovascular_phenotype": 3,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 4,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 12,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiomyopathy": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 10,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 12,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 5,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 2,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiovascular_phenotype": 3,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 10,
    "Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_specified|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 2,
    "FLNC-related_disorder|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 4,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 7,
    "not_specified|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 10,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified": 1,
    "FLNC-related_disorder|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 4,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 2,
    "not_specified|not_provided|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 7,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 3,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 2,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 3,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 8,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 5,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 2,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|FLNC-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 4,
    "Cardiovascular_phenotype|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_specified|not_provided|Cardiomyopathy": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 2,
    "Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype": 12,
    "Cardiovascular_phenotype|not_provided|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 2,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 10,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 2,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 6,
    "not_provided|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 2,
    "not_specified|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 2,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 12,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 3,
    "FLNC-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|Cardiovascular_phenotype": 2,
    "Primary_dilated_cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 4,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 7,
    "not_provided|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 3,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|FLNC-related_disorder|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided": 4,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 8,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 8,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 3,
    "not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 3,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|not_specified": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "not_specified|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 6,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 13,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|FLNC-related_disorder|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 4,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|FLNC-related_disorder|not_specified|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 3,
    "not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 5,
    "Primary_familial_hypertrophic_cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided": 2,
    "not_specified|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 4,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 3,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided|See_cases": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 3,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "not_specified|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 2,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|FLNC-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 2,
    "FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided": 2,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|FLNC-related_disorder|not_provided": 1,
    "not_provided|not_specified|FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype": 4,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 2,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 5,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 8,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 4,
    "not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 3,
    "FLNC-related_disorder|not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|not_provided": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "not_specified|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "not_provided|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 2,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 2,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|not_provided": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiomyopathy|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 7,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_specified|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 3,
    "not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|FLNC-related_disorder|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 4,
    "not_specified|Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 1,
    "FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 2,
    "Cardiovascular_phenotype|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided": 5,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified": 2,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided": 5,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 5,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 4,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 4,
    "not_specified|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 3,
    "Cardiovascular_phenotype|not_provided|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "FLNC-related_disorder|not_provided": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 3,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_1|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 7,
    "not_provided|Myofibrillar_myopathy_5": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 2,
    "FLNC-related_disorder|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder|not_specified": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 3,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|FLNC-related_disorder|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Wolff-Parkinson-White_pattern|not_provided": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 2,
    "not_specified|FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "FLNC-related_disorder|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|FLNC-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 4,
    "FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiomyopathy|not_provided": 1,
    "See_cases|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|FLNC-related_disorder": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype": 3,
    "not_specified|FLNC-related_disorder|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided": 2,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided": 5,
    "not_specified|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder": 1,
    "FLNC-related_disorder|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Limb-girdle_muscular_dystrophy": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Abnormality_of_the_musculature": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 3,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|FLNC-related_disorder|Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 2,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided": 2,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|FLNC-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|FLNC-related_disorder|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_specified": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 5,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 4,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|FLNC-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Cardiomyopathy|not_specified|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 3,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_specified": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 4,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Primary_familial_dilated_cardiomyopathy|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 2,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|FLNC-related_disorder|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|FLNC-related_disorder": 2,
    "Cardiovascular_phenotype|FLNC-related_disorder|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified|Cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26": 2,
    "Cardiovascular_phenotype|not_specified|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided": 7,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 2,
    "Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Hypertrophic_cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 2,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 3,
    "not_provided|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|FLNC-related_disorder|not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 2,
    "not_provided|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|FLNC-related_disorder|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 3,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 2,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|FLNC-related_disorder": 1,
    "not_provided|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "Disorder_of_cardiovascular_system": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|FLNC-related_disorder|not_specified": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 2,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|not_specified|FLNC-related_disorder|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 1,
    "FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Cardiomyopathy|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 1,
    "FLNC-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiomyopathy|_familial_restrictive|_5": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 2,
    "not_provided|Primary_dilated_cardiomyopathy|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|_familial_restrictive|_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 2,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|not_specified": 1,
    "FLNC-related_disorder|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_specified": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified|not_provided|FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 1,
    "FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_specified|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Primary_dilated_cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "not_provided|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "FLNC-associated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_26|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Primary_familial_hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 3,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_specified|not_provided|Dilated_Cardiomyopathy|_Dominant": 1,
    "Spastic_ataxia|Cerebellar_ataxia": 1,
    "not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Primary_familial_dilated_cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26": 2,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_provided|Dilated_Cardiomyopathy|_Dominant": 1,
    "See_cases|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 2,
    "not_provided|Cardiovascular_phenotype|FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant": 1,
    "Primary_familial_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|not_provided": 1,
    "FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Conduction_disorder_of_the_heart": 1,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 2,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_specified": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified": 3,
    "not_specified|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|FLNC-related_disorder|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|FLNC-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Asymmetric_septal_hypertrophy": 1,
    "not_specified|Cardiomyopathy|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|FLNC-related_disorder": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Restrictive_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|not_specified|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_specified": 2,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|FLNC-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_5|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_26|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_specified|Cardiomyopathy|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "not_provided|Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "Myofibrillar_myopathy_5": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Primary_familial_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_15": 1,
    "FLNC-related_disorder|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|FLNC-related_disorder|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|FLNC-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype|FLNC-related_disorder": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder|not_provided": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "Wolff-Parkinson-White_pattern|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_specified": 1,
    "FLNC-related_disorder|not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_specified": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "Restrictive_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_provided|FLNC-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "not_provided|not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiomyopathy": 1,
    "not_specified|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant": 2,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|FLNC-related_disorder|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|FLNC-related_disorder|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Cardiovascular_phenotype|FLNC-related_disorder|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|FLNC-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|Cardiovascular_phenotype": 1,
    "FLNC-related_disorder|not_provided|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5": 1,
    "Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|not_provided|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26": 1,
    "Abnormal_ventricular_septum_morphology|Facial_asymmetry|Two-raphe_bicuspid_aortic_valve|Abnormal_morphology_of_left_ventricular_trabeculae|Episodic_vomiting|Patent_foramen_ovale|Asymmetry_of_the_thorax": 1,
    "Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Primary_familial_dilated_cardiomyopathy|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_26|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Primary_familial_dilated_cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|not_specified": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_specified|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_15|not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_26|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|Myofibrillar_myopathy_5": 1,
    "Myofibrillar_myopathy|not_provided|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_26|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_5|Distal_myopathy_with_posterior_leg_and_anterior_hand_involvement|not_provided": 1,
    "Inflammatory_bowel_disease_14|_susceptibility_to|Systemic_lupus_erythematosus|_susceptibility_to|_10": 1,
    "Rheumatoid_arthritis|Systemic_lupus_erythematosus|_susceptibility_to|_10|Systemic_lupus_erythematosus": 1,
    "IRF5-related_disorder": 1,
    "Systemic_lupus_erythematosus|_susceptibility_to|_10": 2,
    "SYSTEMIC_LUPUS_ERYTHEMATOSUS|_ASSOCIATION_WITH_SUSCEPTIBILITY_TO|_10": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided": 29,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 450,
    "not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 4,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|Muscular_dystrophy|_limb-girdle|_autosomal_dominant": 1,
    "TNPO3-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided": 3,
    "not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 30,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 2,
    "not_provided|not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 4,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_specified|not_provided": 5,
    "not_specified|not_provided|TNPO3-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 1,
    "TNPO3-related_disorder": 2,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided": 3,
    "not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_specified": 9,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided|not_specified": 2,
    "not_specified|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 2,
    "not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 12,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|TNPO3-related_disorder": 3,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|Inborn_genetic_diseases|not_provided": 1,
    "TNPO3-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F": 1,
    "Scapular_winging": 2,
    "TNPO3-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided": 1,
    "TNPO3-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_specified": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1F|not_provided|TNPO3-related_disorder": 1,
    "SMO-related_disorder|not_provided": 2,
    "Hamartoma_of_hypothalamus": 18,
    "Hamartoma_of_hypothalamus|Inborn_genetic_diseases": 2,
    "not_provided|Hamartoma_of_hypothalamus": 2,
    "SMO-related_disorder": 8,
    "not_specified|Hamartoma_of_hypothalamus": 1,
    "SMO-related_disorder|not_specified|not_provided": 2,
    "SMO-related_disorder|Microcephaly|not_provided": 1,
    "not_provided|Curry-Jones_syndrome": 1,
    "Hamartoma_of_hypothalamus|not_provided": 4,
    "not_provided|SMO-related_disorder|Curry-Jones_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Hamartoma_of_hypothalamus": 1,
    "Curry-Jones_syndrome": 3,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Curry-Jones_syndrome|Hamartoma_of_hypothalamus": 1,
    "not_provided|Hamartoma_of_hypothalamus|not_specified": 1,
    "not_specified|not_provided|Hamartoma_of_hypothalamus": 1,
    "Hamartoma_of_hypothalamus|not_specified": 2,
    "Curry-Jones_syndrome|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_50": 2,
    "MIR96-related_condition|not_specified": 1,
    "UBE2H-related_disorder": 4,
    "not_provided|CPA4-related_disorder": 1,
    "Hereditary_pancreatitis|CPA1-related_disorder|not_provided": 4,
    "CPA1-related_disorder|Hereditary_pancreatitis|not_provided": 2,
    "CPA1-related_disorder|not_provided|Hereditary_pancreatitis": 3,
    "not_provided|CPA1-related_disorder|Hereditary_pancreatitis": 1,
    "not_provided|Hereditary_pancreatitis|Early-onset_chronic_pancreatitis": 1,
    "not_provided|Joubert_syndrome_15": 16,
    "Joubert_syndrome_15": 305,
    "Joubert_syndrome_15|not_provided": 11,
    "Joubert_syndrome_15|Joubert_syndrome_9/15|_digenic": 1,
    "Joubert_syndrome_15|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_15": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_15": 11,
    "not_provided|CEP41-related_disorder|Joubert_syndrome_15": 1,
    "Familial_Autism_Spectrum_Disorder|not_provided|Joubert_syndrome_15": 1,
    "CEP41-related_disorder|Joubert_syndrome_15": 2,
    "Joubert_syndrome|Joubert_syndrome_15|not_specified": 1,
    "Joubert_syndrome_15|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome_15|Familial_Autism_Spectrum_Disorder": 2,
    "not_specified|not_provided|Joubert_syndrome_15": 3,
    "Joubert_syndrome_15|Joubert_syndrome": 1,
    "Joubert_syndrome_15|CEP41-related_disorder": 1,
    "CEP41-related_disorder|not_provided|Familial_Autism_Spectrum_Disorder|not_specified|Intellectual_disability|Joubert_syndrome_15": 1,
    "Familial_Autism_Spectrum_Disorder|Joubert_syndrome_15": 1,
    "Familial_Autism_Spectrum_Disorder": 1,
    "not_specified|Joubert_syndrome_15": 3,
    "Joubert_syndrome_15|not_provided|not_specified": 1,
    "CEP41-related_disorder": 3,
    "Joubert_syndrome_15|JOUBERT_SYNDROME_12/15|_DIGENIC": 1,
    "CEP41-related_disorder|Joubert_syndrome_15|not_provided": 2,
    "Joubert_syndrome_15|not_specified": 1,
    "Joubert_syndrome_15|not_specified|CEP41-related_disorder|not_provided": 1,
    "not_provided|Joubert_syndrome_15|Familial_Autism_Spectrum_Disorder": 1,
    "Joubert_syndrome_15|not_provided|Joubert_syndrome_9/15|_digenic|Familial_Autism_Spectrum_Disorder": 1,
    "not_provided|CEP41-related_disorder": 1,
    "Joubert_syndrome_15|not_provided|CEP41-related_disorder": 1,
    "KLF14-related_disorder": 1,
    "LINC-PINT-related_disorder": 5,
    "PODXL-related_disorder": 4,
    "PODXL-related_disorder|not_provided": 6,
    "not_provided|PODXL-related_disorder": 9,
    "PODXL-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "PODXL-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|PODXL-related_disorder|not_provided": 1,
    "Nephrotic_syndrome|not_specified|not_provided|PODXL-related_disorder": 1,
    "PLXNA4-related_disorder": 533,
    "not_provided|PLXNA4-related_disorder": 6,
    "PLXNA4-related_disorder|not_provided": 7,
    "not_specified|PLXNA4-related_disorder": 23,
    "PLXNA4-related_disorder|not_specified": 8,
    "Congenital_myotonia|_autosomal_recessive_form": 32,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 6,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12": 10,
    "Deficiency_of_bisphosphoglycerate_mutase": 5,
    "not_provided|Deficiency_of_bisphosphoglycerate_mutase": 1,
    "Deficiency_of_bisphosphoglycerate_mutase|not_provided": 1,
    "Neurodevelopmental_disorder_with_brain_malformations_and_multiple_congenital_anomalies": 1,
    "NUP205-related_disorder|not_provided": 12,
    "not_provided|NUP205-related_disorder|Nephrotic_syndrome|_type_13": 1,
    "Nephrotic_syndrome|_type_13|not_provided": 1,
    "Nephrotic_syndrome|_type_13|not_specified": 2,
    "NUP205-related_disorder": 11,
    "not_specified|NUP205-related_disorder": 2,
    "not_provided|Nephrotic_syndrome|_type_13": 4,
    "Nephrotic_syndrome|_type_13": 5,
    "not_provided|NUP205-related_disorder": 4,
    "not_specified|not_provided|Nephrotic_syndrome|_type_13": 1,
    "NUP205-related_disorder|not_specified|not_provided": 1,
    "NUP205-related_disorder|not_specified": 1,
    "Nephrotic_syndrome|_type_13|not_provided|NUP205-related_disorder": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_specified": 37,
    "not_specified|Dilated_Cardiomyopathy|_Dominant": 29,
    "Dilated_Cardiomyopathy|_Dominant|not_provided": 14,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|not_specified": 3,
    "not_provided|not_specified|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|not_specified": 2,
    "not_provided|Dilated_Cardiomyopathy|_Dominant": 9,
    "not_specified|not_provided|CHRM2-related_disorder|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided": 3,
    "Congenital_bile_acid_synthesis_defect_2": 84,
    "not_provided|AKR1D1-related_disorder": 4,
    "AKR1D1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "AKR1D1-related_disorder": 13,
    "Congenital_bile_acid_synthesis_defect_2|not_provided": 11,
    "not_provided|Congenital_bile_acid_synthesis_defect_2": 9,
    "AKR1D1-related_disorder|not_provided": 3,
    "Congenital_bile_acid_synthesis_defect_2|not_provided|not_specified": 2,
    "not_specified|not_provided|Congenital_bile_acid_synthesis_defect_2": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_bile_acid_synthesis_defect_2": 1,
    "Inborn_genetic_diseases|Congenital_bile_acid_synthesis_defect_2": 2,
    "Congenital_bile_acid_synthesis_defect_2|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Congenital_bile_acid_synthesis_defect_2": 2,
    "not_specified|Congenital_bile_acid_synthesis_defect_2": 1,
    "Congenital_bile_acid_synthesis_defect_2|Congenital_bile_acid_synthesis_defect": 1,
    "not_specified|Congenital_bile_acid_synthesis_defect_2|not_provided": 1,
    "Congenital_bile_acid_synthesis_defect": 1,
    "TRIM24-related_disorder": 1,
    "not_provided|Autosomal_recessive_distal_renal_tubular_acidosis": 26,
    "Autosomal_recessive_distal_renal_tubular_acidosis": 28,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 2,
    "not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Autosomal_recessive_distal_renal_tubular_acidosis": 2,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 108,
    "not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 15,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided|Autosomal_recessive_distal_renal_tubular_acidosis": 3,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided": 16,
    "ATP6V0A4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided": 2,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Inborn_genetic_diseases|not_provided": 2,
    "ATP6V0A4-related_disorder": 3,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Inborn_genetic_diseases": 2,
    "ATP6V0A4-related_disorder|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 2,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 2,
    "Autosomal_recessive_distal_renal_tubular_acidosis|not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 3,
    "not_provided|Autosomal_recessive_distal_renal_tubular_acidosis|ATP6V0A4-related_disorder": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Inborn_genetic_diseases": 9,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Inborn_genetic_diseases|not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Autosomal_recessive_distal_renal_tubular_acidosis|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Autosomal_recessive_distal_renal_tubular_acidosis|not_specified": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|ATP6V0A4-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 7,
    "not_specified|not_provided|Autosomal_recessive_distal_renal_tubular_acidosis": 4,
    "Autosomal_recessive_distal_renal_tubular_acidosis|not_provided": 4,
    "ATP6V0A4-related_disorder|not_provided": 3,
    "not_specified|Autosomal_recessive_distal_renal_tubular_acidosis|not_provided": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided|Inborn_genetic_diseases": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Autosomal_recessive_distal_renal_tubular_acidosis": 5,
    "not_provided|Autosomal_recessive_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_specified": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Autosomal_recessive_distal_renal_tubular_acidosis|not_provided": 2,
    "not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided|Autosomal_recessive_distal_renal_tubular_acidosis|not_specified": 1,
    "Renal_tubular_acidosis_with_progressive_nerve_deafness|Autosomal_recessive_distal_renal_tubular_acidosis|not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "Inborn_genetic_diseases|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_distal_renal_tubular_acidosis|Distal_Renal_Tubular_Acidosis|_Recessive": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided|not_specified": 1,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided|Inborn_genetic_diseases": 2,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Distal_renal_tubular_acidosis|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Inborn_genetic_diseases|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "Inborn_genetic_diseases|not_specified|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "Autosomal_recessive_distal_renal_tubular_acidosis|ATP6V0A4-related_disorder|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided": 1,
    "Autosomal_recessive_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_specified": 1,
    "not_provided|ATP6V0A4-related_disorder": 1,
    "ATP6V0A4-related_disorder|Autosomal_recessive_distal_renal_tubular_acidosis|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "ATP6V0A4-related_disorder|not_provided|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Inborn_genetic_diseases|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "not_provided|Renal_tubulopathies|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Sensorineural_hearing_loss_disorder": 1,
    "not_provided|not_specified|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|Autosomal_recessive_distal_renal_tubular_acidosis|not_specified|not_provided": 1,
    "ATP6V0A4-related_disorder|Renal_tubular_acidosis|_distal|_3|_with_or_without_sensorineural_hearing_loss|not_provided": 1,
    "Bailey-Bloch_congenital_myopathy|not_provided|not_specified|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "KIAA1549-related_disorder": 6,
    "KIAA1549-related_disorder|not_provided": 12,
    "Retinitis_pigmentosa_86|not_provided": 9,
    "not_provided|KIAA1549-related_disorder": 14,
    "KIAA1549-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_86": 6,
    "not_provided|Retinitis_pigmentosa_86|not_specified": 1,
    "Retinitis_pigmentosa_86": 6,
    "Retinitis_pigmentosa_86|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_86|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|KIAA1549-related_disorder": 1,
    "Retinitis_pigmentosa_86|not_provided|Retinal_dystrophy": 3,
    "Retinal_dystrophy|not_provided|KIAA1549-related_disorder": 1,
    "KIAA1549-related_disorder|not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_86": 2,
    "Retinal_dystrophy|KIAA1549-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|KIAA1549-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_86|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_86|Inborn_genetic_diseases": 2,
    "Optic_atrophy|KIAA1549-related_disorder|not_provided": 1,
    "not_provided|Optic_atrophy|Inborn_genetic_diseases": 2,
    "KIAA1549-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Biliary|_renal|_neurologic|_and_skeletal_syndrome|not_provided|Hydrocephalus": 1,
    "Biliary|_renal|_neurologic|_and_skeletal_syndrome": 3,
    "Biliary|_renal|_neurologic|_and_skeletal_syndrome|Caroli_disease": 1,
    "IFT56-related_disorder|not_provided": 1,
    "not_specified|UBN2-related_disorder": 1,
    "UBN2-related_disorder": 17,
    "UBN2-related_disorder|not_provided": 1,
    "not_provided|UBN2-related_disorder": 1,
    "UBN2_associated_Autism_susceptibility": 1,
    "UBN2-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|TBXAS1-related_disorder": 1,
    "Ghosal_hematodiaphyseal_dysplasia": 12,
    "Ghosal_hematodiaphyseal_dysplasia|not_provided": 3,
    "TBXAS1-related_disorder|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Ghosal_hematodiaphyseal_dysplasia": 1,
    "TBXAS1-related_disorder": 3,
    "not_provided|Ghosal_hematodiaphyseal_dysplasia": 6,
    "Thromboxane_synthetase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Ghosal_hematodiaphyseal_dysplasia|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability": 1,
    "not_specified|TBXAS1-related_disorder|not_provided": 2,
    "not_provided|TBXAS1-related_disorder": 5,
    "TBXAS1-related_disorder|not_provided": 4,
    "Thromboxane_synthetase_deficiency|Ghosal_hematodiaphyseal_dysplasia": 1,
    "not_specified|not_provided|TBXAS1-related_disorder": 1,
    "Ghosal_hematodiaphyseal_dysplasia|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Ghosal_hematodiaphyseal_dysplasia|not_provided": 2,
    "not_provided|Ghosal_hematodiaphyseal_dysplasia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Ghosal_hematodiaphyseal_dysplasia": 1,
    "not_specified|TBXAS1-related_disorder|Ghosal_hematodiaphyseal_dysplasia|not_provided": 1,
    "not_provided|not_specified|TBXAS1-related_disorder": 1,
    "Ghosal_hematodiaphyseal_dysplasia|Thromboxane_synthetase_deficiency|not_specified|not_provided": 1,
    "not_specified|Ghosal_hematodiaphyseal_dysplasia|not_provided|Abnormal_bleeding|Thrombocytopenia|Inborn_genetic_diseases": 1,
    "Ghosal_hematodiaphyseal_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "ADCK2-related_disorder": 2,
    "ADCK2-related_disorder|not_provided": 1,
    "Noonan_syndrome_7|LEOPARD_syndrome_3": 6,
    "LEOPARD_syndrome_3|Noonan_syndrome_7": 4,
    "RASopathy|not_specified|Noonan_syndrome_7|LEOPARD_syndrome_3": 1,
    "Cardiofaciocutaneous_syndrome_1": 14,
    "BRAF-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|LEOPARD_syndrome_3|Noonan_syndrome_7|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Lung_cancer|Cardiofaciocutaneous_syndrome_1|RASopathy": 1,
    "RASopathy|Noonan_syndrome_7": 3,
    "RASopathy|BRAF-related_disorder": 6,
    "not_specified|Noonan_syndrome_7|LEOPARD_syndrome_3|not_provided|RASopathy|BRAF-related_disorder|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|not_provided|Cardiofaciocutaneous_syndrome_1": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer": 12,
    "RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Noonan_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1|Lung_cancer|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "RASopathy|not_provided|Cardiofaciocutaneous_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Colorectal_cancer|Lung_cancer|Noonan_syndrome_7|LEOPARD_syndrome_3|Noonan_syndrome|Cardio-facio-cutaneous_syndrome": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_1|not_provided": 2,
    "Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|Cardio-facio-cutaneous_syndrome": 3,
    "not_provided|Intellectual_disability|Noonan_syndrome_and_Noonan-related_syndrome|BRAF-related_disorder|not_specified|RASopathy": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|Congenital_long_QT_syndrome|RASopathy|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|Noonan_syndrome_with_multiple_lentigines|RASopathy|not_specified|Noonan_syndrome": 1,
    "BRAF-related_disorder": 14,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|RASopathy": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Noonan_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "BRAF-related_disorder|RASopathy": 2,
    "not_specified|not_provided|RASopathy|BRAF-related_disorder": 1,
    "BRAF-related_disorder|not_specified|RASopathy": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_1|Lung_cancer|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|RASopathy": 4,
    "not_specified|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|Cardio-facio-cutaneous_syndrome": 1,
    "Cardiovascular_phenotype|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiovascular_phenotype|BRAF-related_disorder|not_specified|not_provided|Cardiofaciocutaneous_syndrome_1|Lung_cancer|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|RASopathy": 1,
    "BRAF-related_disorder|not_provided": 1,
    "Cardiofaciocutaneous_syndrome_1|RASopathy": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Lung_cancer|RASopathy": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Lung_cancer|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1|not_provided|RASopathy": 1,
    "not_specified|not_provided|Cardiofaciocutaneous_syndrome_1|Lung_cancer|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_1|Lung_carcinoma|LEOPARD_syndrome_3|Noonan_syndrome_7|Noonan_syndrome_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|LEOPARD_syndrome_3|not_specified|Noonan_syndrome_7|RASopathy": 1,
    "Inborn_genetic_diseases|Cardio-facio-cutaneous_syndrome|Melanoma|not_provided|RASopathy|Noonan_syndrome_7|Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_1": 1,
    "Inborn_genetic_diseases|Noonan_syndrome_7|LEOPARD_syndrome_3|Cardiofaciocutaneous_syndrome_1|Lung_carcinoma|Noonan_syndrome_1|not_provided|RASopathy": 1,
    "RASopathy|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Noonan_syndrome_1|Colorectal_cancer|Lung_cancer|not_provided|not_specified|RASopathy": 1,
    "Noonan_syndrome_7": 4,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Noonan_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Cardiovascular_phenotype|RASopathy": 1,
    "not_provided|Cardiofaciocutaneous_syndrome_1": 1,
    "not_provided|RASopathy|Endometrial_carcinoma": 1,
    "Cardio-facio-cutaneous_syndrome|not_provided|RASopathy|Noonan_syndrome_7|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiofaciocutaneous_syndrome_1|RASopathy|Noonan_syndrome|Cardio-facio-cutaneous_syndrome": 1,
    "not_provided|Non-small_cell_lung_carcinoma": 1,
    "Lung_adenocarcinoma|Carcinoma_of_colon|Thyroid_cancer|_nonmedullary|_2|Non-small_cell_lung_carcinoma": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Lung_cancer|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy": 1,
    "Melanoma": 4,
    "Cardio-facio-cutaneous_syndrome|not_provided|RASopathy": 2,
    "Vascular_malformation|Lymphangioma|Malignant_neoplastic_disease|Melanoma|Cardiovascular_phenotype|Cystic_epithelial_invagination_containing_papillae_lined_by_columnar_epithelium|Cardio-facio-cutaneous_syndrome|Nephroblastoma|not_provided|RASopathy|Nongerminomatous_germ_cell_tumor|Papillary_thyroid_carcinoma|Multiple_myeloma|Cerebral_arteriovenous_malformation|Non-small_cell_lung_carcinoma|Astrocytoma|_low-grade|_somatic|Carcinoma_of_colon": 1,
    "Non-small_cell_lung_carcinoma|Myoepithelial_tumor": 1,
    "Non-small_cell_lung_carcinoma|not_provided": 2,
    "RASopathy|not_provided|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Lung_cancer": 1,
    "Childhood_ganglioglioma|Non-small_cell_lung_carcinoma|Neoplasm_of_the_large_intestine|not_provided": 1,
    "Cardiofaciocutaneous_syndrome_1|not_provided|Noonan_syndrome|RASopathy": 1,
    "RASopathy|not_provided|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_7|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|Non-small_cell_lung_carcinoma|Noonan_syndrome_1|not_provided|RASopathy|LEOPARD_syndrome_3|Cardiofaciocutaneous_syndrome_1": 1,
    "Inborn_genetic_diseases|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1": 1,
    "not_specified|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardio-facio-cutaneous_syndrome|not_provided|RASopathy|Noonan_syndrome_7": 1,
    "Cardio-facio-cutaneous_syndrome|RASopathy|not_provided|Prostate_cancer|_hereditary|_1|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardio-facio-cutaneous_syndrome": 8,
    "Cardio-facio-cutaneous_syndrome|RASopathy": 1,
    "Non-small_cell_lung_carcinoma|Non-Hodgkin_lymphoma|not_provided|RASopathy|Lung_adenocarcinoma": 1,
    "Prostate_cancer|_hereditary|_1|Lung_adenocarcinoma|Non-small_cell_lung_carcinoma": 1,
    "Gallbladder_cancer": 2,
    "Cardio-facio-cutaneous_syndrome|not_provided|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1|Lung_carcinoma|LEOPARD_syndrome_3|Noonan_syndrome_7": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 2,
    "RASopathy|Prostate_cancer|_hereditary|_1": 3,
    "Cardiovascular_phenotype|Cardio-facio-cutaneous_syndrome|Noonan_syndrome_7|LEOPARD_syndrome_3|Cardiofaciocutaneous_syndrome_1|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "Inborn_genetic_diseases|Cardio-facio-cutaneous_syndrome|not_provided|not_specified|RASopathy|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardio-facio-cutaneous_syndrome|not_provided": 3,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Noonan_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|RASopathy": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_7": 1,
    "Noonan_syndrome|not_provided|Noonan_syndrome_7|RASopathy": 1,
    "not_provided|Cardio-facio-cutaneous_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "RASopathy|not_specified|LEOPARD_syndrome_3|Noonan_syndrome_7": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Lung_cancer|Noonan_syndrome_1|Colorectal_cancer|not_provided": 1,
    "RASopathy|Primary_dilated_cardiomyopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Lung_cancer|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|not_specified": 1,
    "RASopathy|Costello_syndrome|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|RASopathy|not_specified|BRAF-related_disorder": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer|Cardiovascular_phenotype": 1,
    "PHACE_syndrome|Tethered_cord|Genetic_syndrome_with_a_Dandy-Walker_malformation_as_major_feature|Inborn_genetic_diseases|Cardio-facio-cutaneous_syndrome|Dandy-Walker_syndrome|Cardiofaciocutaneous_syndrome_1": 1,
    "not_provided|RASopathy|Noonan_syndrome_7|Noonan_syndrome_1": 1,
    "not_provided|Colorectal_cancer|RASopathy": 1,
    "not_provided|Malignant_lymphoma|_large_B-cell|_diffuse": 1,
    "not_provided|Melanoma|LEOPARD_syndrome_3|Noonan_syndrome_7|Cardiofaciocutaneous_syndrome_1": 1,
    "not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1|Inborn_genetic_diseases": 1,
    "Noonan_syndrome_7|LEOPARD_syndrome_3|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiofaciocutaneous_syndrome_1|Cardio-facio-cutaneous_syndrome|not_provided|RASopathy": 1,
    "Cardio-facio-cutaneous_syndrome|Neonatal_respiratory_distress|Ventricular_hypertrophy|Downslanted_palpebral_fissures|Premature_birth|Wide_intermamillary_distance|Webbed_neck|Ventricular_septal_defect|Pulmonic_stenosis|High_forehead|Low-set|_posteriorly_rotated_ears|RASopathy|not_provided|Familial_cardiofaciocutaneous_syndrome|Cardiofaciocutaneous_syndrome_1": 1,
    "not_provided|RASopathy|Noonan_syndrome|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|RASopathy|Cardiofaciocutaneous_syndrome_1": 1,
    "Lung_cancer|Noonan_syndrome_7|LEOPARD_syndrome_3|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy": 1,
    "Costello_syndrome": 367,
    "Dabrafenib_response": 1,
    "RASopathy|Cardio-facio-cutaneous_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiovascular_phenotype|BRAF-related_disorder|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1|Ataxia-telangiectasia_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_7|Noonan_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Lung_cancer|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Cardio-facio-cutaneous_syndrome|not_provided|RASopathy": 1,
    "RASopathy|Cardio-facio-cutaneous_syndrome|Noonan_syndrome": 1,
    "RASopathy|Cardio-facio-cutaneous_syndrome": 2,
    "not_provided|Cardio-facio-cutaneous_syndrome": 2,
    "Neurodevelopmental_delay|Cardiofaciocutaneous_syndrome_1|Cardio-facio-cutaneous_syndrome": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|RASopathy": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Lung_cancer|Cardiofaciocutaneous_syndrome_1|RASopathy": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_1|Lung_cancer|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|RASopathy|not_specified": 1,
    "not_provided|RASopathy|Ataxia-telangiectasia_syndrome": 1,
    "Non-small_cell_lung_carcinoma|Non-Hodgkin_lymphoma": 1,
    "Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|not_specified|not_provided|Noonan_syndrome_7|RASopathy|Noonan_syndrome_1": 1,
    "Non-Hodgkin_lymphoma|Cardio-facio-cutaneous_syndrome|not_provided": 1,
    "Non-small_cell_lung_carcinoma|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "See_cases|Cardio-facio-cutaneous_syndrome|not_provided|BRAF-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Cardiofaciocutaneous_syndrome_1": 1,
    "Noonan_syndrome_7|Epidermal_nevus|RASopathy": 1,
    "Non-small_cell_lung_carcinoma|not_provided|Vascular_malformation": 1,
    "Non-small_cell_lung_carcinoma|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiofaciocutaneous_syndrome_1|Cardio-facio-cutaneous_syndrome": 1,
    "Cardio-facio-cutaneous_syndrome|RASopathy|Noonan_syndrome|not_provided|Carcinoma_of_colon": 1,
    "not_provided|RASopathy|Prostate_cancer|_hereditary|_1|Cardio-facio-cutaneous_syndrome": 1,
    "Noonan_syndrome_7|not_provided": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|LEOPARD_syndrome_3|Noonan_syndrome_7|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiovascular_phenotype|RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Lung_cancer|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Lung_cancer|RASopathy": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_1|Lung_cancer|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Cardiovascular_phenotype|RASopathy": 1,
    "Prostate_cancer|_hereditary|_1|RASopathy": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|LEOPARD_syndrome_3|RASopathy|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer|RASopathy": 4,
    "BRAF-related_disorder|not_provided|RASopathy": 2,
    "not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1|Lung_cancer|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Noonan_syndrome_1|Colorectal_cancer|Lung_cancer|not_provided|RASopathy": 1,
    "RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Lung_cancer": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_1": 3,
    "Noonan_syndrome_7|RASopathy|LEOPARD_syndrome_3|Colorectal_cancer|Lung_cancer|Cardiofaciocutaneous_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|LEOPARD_syndrome_3|Noonan_syndrome_7": 1,
    "not_specified|RASopathy|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|BRAF-related_disorder|not_specified|RASopathy": 1,
    "not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Lung_cancer|Colorectal_cancer|Noonan_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|RASopathy|not_specified": 1,
    "not_provided|RASopathy|Noonan_syndrome|Hypertrophic_cardiomyopathy|Lung_cancer|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|RASopathy": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7": 1,
    "RASopathy|Noonan_syndrome_7|LEOPARD_syndrome_3|Lung_cancer|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Lung_carcinoma|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Noonan_syndrome_1|RASopathy": 1,
    "not_specified|RASopathy|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|LEOPARD_syndrome_3": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_7|LEOPARD_syndrome_3": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Lung_cancer|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1|RASopathy": 1,
    "Noonan_syndrome|LEOPARD_syndrome_3|Noonan_syndrome_7|Cardiovascular_phenotype": 1,
    "not_provided|Noonan_syndrome_7|LEOPARD_syndrome_3|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiofaciocutaneous_syndrome_1|Colorectal_cancer|Lung_cancer|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_7|LEOPARD_syndrome_3|not_specified": 1,
    "RASopathy|not_specified|BRAF-related_disorder|Cardiovascular_phenotype": 2,
    "not_specified|RASopathy|Noonan_syndrome|Cardiofaciocutaneous_syndrome_1|Colorectal_cancer|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Cardiovascular_phenotype": 1,
    "not_provided|RASopathy|Noonan_syndrome_7|LEOPARD_syndrome_3": 1,
    "LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|Noonan_syndrome_1|not_specified|RASopathy": 3,
    "not_provided|RASopathy|Noonan_syndrome": 1,
    "not_specified|not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|BRAF-related_disorder": 1,
    "RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7": 1,
    "BRAF-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy|not_specified": 1,
    "LEOPARD_syndrome_3": 1,
    "not_provided|Colorectal_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_1|Cardiovascular_phenotype|RASopathy": 1,
    "Cardio-facio-cutaneous_syndrome|RASopathy|Noonan_syndrome|not_provided": 1,
    "Cardiofaciocutaneous_syndrome_1|RASopathy|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Lung_cancer|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|BRAF-related_disorder|Cardio-facio-cutaneous_syndrome|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "RASopathy|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Global_developmental_delay|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_provided": 1,
    "RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 2,
    "not_provided|Noonan_syndrome|Cardio-facio-cutaneous_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1|not_provided|Noonan_syndrome_7|Noonan_syndrome|RASopathy": 1,
    "Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|Noonan_syndrome_7|Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_1|RASopathy": 1,
    "not_provided|Neurodevelopmental_delay|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|not_provided|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_1|Lung_carcinoma|LEOPARD_syndrome_3|Noonan_syndrome_7|RASopathy": 1,
    "not_provided|RASopathy|Cardio-facio-cutaneous_syndrome": 1,
    "RASopathy|BRAF-related_disorder|Noonan_syndrome|Noonan_syndrome_7|Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_1|not_provided|Cardio-facio-cutaneous_syndrome|Lung_carcinoma|LEOPARD_syndrome_3": 1,
    "not_provided|Noonan_syndrome_7|Inborn_genetic_diseases|RASopathy|Noonan_syndrome_1": 1,
    "Noonan_syndrome_7|LEOPARD_syndrome_3|Cardiofaciocutaneous_syndrome_1|Lung_carcinoma|Noonan_syndrome_1|Cardio-facio-cutaneous_syndrome|not_provided|Noonan_syndrome_with_multiple_lentigines|RASopathy": 1,
    "not_provided|BRAF-related_disorder": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|RASopathy|not_provided|LEOPARD_syndrome_3": 1,
    "RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1": 1,
    "not_specified|BRAF-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "not_provided|Cardiofaciocutaneous_syndrome_1|Colorectal_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|Cardiovascular_phenotype": 1,
    "Cardiofaciocutaneous_syndrome_1|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|not_specified|RASopathy": 1,
    "not_provided|RASopathy|Cardiovascular_phenotype|not_specified|BRAF-related_disorder": 1,
    "not_specified|RASopathy|Noonan_syndrome_7|LEOPARD_syndrome_3": 1,
    "not_specified|not_provided|RASopathy|Lung_carcinoma|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1|Lung_cancer|Noonan_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_specified": 1,
    "not_specified|BRAF-related_disorder|not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Noonan_syndrome_7|LEOPARD_syndrome_3": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|RASopathy": 1,
    "BRAF-related_disorder|RASopathy|not_provided|Cardiovascular_phenotype": 1,
    "RASopathy|not_specified|Noonan_syndrome_7|LEOPARD_syndrome_3|not_provided": 1,
    "RASopathy|not_provided|BRAF-related_disorder|Cardiovascular_phenotype": 1,
    "BRAF-related_spectrum_disorder": 1,
    "RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|not_provided": 1,
    "Noonan_syndrome_7|Cardiovascular_phenotype|not_provided|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|RASopathy": 1,
    "RASopathy|not_provided|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|RASopathy": 1,
    "BRAF-related_disorder|RASopathy|Cardiovascular_phenotype": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Lung_cancer|Cardiofaciocutaneous_syndrome_1|Colorectal_cancer|RASopathy": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_1|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype|not_specified": 4,
    "Noonan_syndrome_and_Noonan-related_syndrome|BRAF-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "BRAF-related_disorder|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|RASopathy|not_provided|not_specified": 1,
    "Noonan_syndrome|RASopathy|BRAF-related_disorder|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 3,
    "BRAF-related_disorder|Cardiovascular_phenotype": 2,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|BRAF-related_disorder": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_1|Noonan_syndrome_with_multiple_lentigines|BRAF-related_disorder": 1,
    "RASopathy|Cardiovascular_phenotype|BRAF-related_disorder": 1,
    "not_specified|Cardiofaciocutaneous_syndrome_1|not_provided|Noonan_syndrome|LEOPARD_syndrome_3|Noonan_syndrome_7|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy": 1,
    "not_provided|not_specified|RASopathy|Noonan_syndrome_7|LEOPARD_syndrome_3": 1,
    "BRAF-related_disorder|RASopathy|not_specified": 1,
    "BRAF-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|RASopathy|Cardiomyopathy|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|BRAF-related_disorder": 1,
    "RASopathy|not_provided|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Lung_cancer|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiofaciocutaneous_syndrome_1|RASopathy|not_specified": 1,
    "BRAF-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|LEOPARD_syndrome_3|Noonan_syndrome_7|RASopathy|not_provided": 1,
    "RASopathy|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Noonan_syndrome_1|Lung_cancer|LEOPARD_syndrome_3|Noonan_syndrome_7|Colorectal_cancer|Cardiofaciocutaneous_syndrome_1|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_7|LEOPARD_syndrome_3|BRAF-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided": 1,
    "not_specified|RASopathy|LEOPARD_syndrome_3|Noonan_syndrome_7|not_provided": 1,
    "Noonan_syndrome_7|LEOPARD_syndrome_3|not_provided": 1,
    "Sengers_syndrome|Developmental_cataract": 4,
    "Sengers_syndrome|not_provided|Developmental_cataract": 1,
    "Sengers_syndrome|Cataract_38": 102,
    "not_provided|Cataract_38|Sengers_syndrome": 8,
    "AGK-related_disorder": 4,
    "Sengers_syndrome|not_provided": 1,
    "AGK-related_disorder|Sengers_syndrome|Cataract_38|not_provided": 4,
    "Sengers_syndrome|Cataract_38|not_specified": 4,
    "AGK-related_disorder|Sengers_syndrome|Cataract_38": 1,
    "Inborn_genetic_diseases|Cataract_38|Sengers_syndrome": 3,
    "Cataract_38|Sengers_syndrome|not_provided|AGK-related_disorder|Inborn_genetic_diseases": 1,
    "Cataract_38|Sengers_syndrome": 85,
    "Cataract_38|Sengers_syndrome|Mitochondrial_disease|Inborn_genetic_diseases": 1,
    "Sengers_syndrome": 18,
    "AGK-related_disorder|Cataract_38|Sengers_syndrome|not_specified|not_provided": 1,
    "Sengers_syndrome|Cataract_38|not_provided": 7,
    "Sengers_syndrome|Cataract_38|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Sengers_syndrome|Cataract_38": 3,
    "not_provided|Cataract_38|Sengers_syndrome|AGK-related_disorder": 1,
    "Cataract_38|Sengers_syndrome|not_provided": 7,
    "Sengers_syndrome|Cataract_38|not_provided|Inborn_genetic_diseases": 2,
    "Trichohepatoenteric_syndrome_1|not_provided|Cataract_38|Sengers_syndrome": 1,
    "not_specified|not_provided|Sengers_syndrome|Cataract_38": 1,
    "AGK-related_disorder|Cataract_38|Sengers_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_AGK-related_phenotype|Sengers_syndrome|Cataract_38": 1,
    "not_provided|Cataract_38|Sengers_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Sengers_syndrome|Cataract_38": 4,
    "AGK-related_disorder|Sengers_syndrome": 1,
    "Cataract_38|Sengers_syndrome|not_specified": 4,
    "AGK-related_disorder|not_provided|Cataract_38|Sengers_syndrome": 1,
    "Cataract_38|Sengers_syndrome|Mitochondrial_disease": 1,
    "AGK-related_disorder|not_specified|Sengers_syndrome|Cataract_38": 1,
    "Inborn_genetic_diseases|Sengers_syndrome|Cataract_38|not_provided": 1,
    "AGK-related_disorder|Cataract_38|Sengers_syndrome": 1,
    "Cataract_38|Sengers_syndrome|not_specified|AGK-related_disorder": 1,
    "Cataract_38|Inborn_genetic_diseases|Sengers_syndrome|not_provided": 1,
    "Cataract_38|Sengers_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Cataract_38|Sengers_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Sengers_syndrome|Cataract_38|not_provided": 1,
    "Cataract_38|Sengers_syndrome|Inborn_genetic_diseases": 2,
    "not_specified|Cataract_38|Sengers_syndrome": 1,
    "Developmental_cataract|Sengers_syndrome": 7,
    "WEE2-related_disorder": 5,
    "WEE2-related_disorder|Oocyte_maturation_defect_5": 1,
    "Oocyte_maturation_defect_5": 6,
    "not_provided|WEE2-related_disorder": 1,
    "Cone-rod_dystrophy|Optic_atrophy_13_with_retinal_and_foveal_abnormalities": 1,
    "Optic_atrophy_13_with_retinal_and_foveal_abnormalities": 2,
    "Optic_atrophy_13_with_retinal_and_foveal_abnormalities|not_provided": 1,
    "Phenylthiocarbamide_tasting": 2,
    "not_provided|Phenylthiocarbamide_tasting": 1,
    "not_specified|MGAM-related_disorder": 3,
    "MGAM-related_disorder|not_provided": 1,
    "MGAM-related_disorder|not_specified": 2,
    "MGAM-related_disorder": 20,
    "PRSS1-related_disorder|Hereditary_pancreatitis": 1,
    "not_provided|Hereditary_pancreatitis|Recurrent_pancreatitis": 1,
    "Myoepithelial_tumor|PRSS1-related_disorder|Trypsinogen_deficiency|Hereditary_pancreatitis|not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia": 1,
    "Hereditary_pancreatitis|Trypsinogen_deficiency": 1,
    "PRSS1-related_disorder|not_provided|Hereditary_pancreatitis": 2,
    "Pancreatitis|_chronic|_protection_against": 1,
    "TRPV6-related_disorder": 2,
    "TRPV6-related_disorder|not_provided": 8,
    "not_provided|TRPV6-related_disorder": 13,
    "Slender_long_bone|Hyperparathyroidism|Embryonic_calcium_dysregulation|Metaphyseal_fractures": 1,
    "Inborn_genetic_diseases|Hyperparathyroidism|_transient_neonatal|not_provided": 1,
    "Hyperparathyroidism|_transient_neonatal|not_provided": 4,
    "Hyperparathyroidism|_transient_neonatal": 13,
    "not_provided|Hyperparathyroidism|_transient_neonatal": 1,
    "Hyperparathyroidism|_transient_neonatal|TRPV6-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hyperparathyroidism|_transient_neonatal": 1,
    "TRPV5-related_disorder": 2,
    "Renal_Calcium_Wasting_Hypercalciuria": 1,
    "Kell_blood_group_system": 5,
    "KEL-related_disorder": 7,
    "Kel6_antigen|not_provided": 1,
    "not_specified|Kell_blood_group_system": 1,
    "KEL-related_disorder|not_provided": 1,
    "Vein_of_Galen_arteriovenous_malformations": 2,
    "KELL_K/k_BLOOD_GROUP_POLYMORPHISM|not_provided": 1,
    "KELL-NULL_PHENOTYPE": 1,
    "CASP2-related_disorder": 5,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_recessive_80|_with_variant_lissencephaly": 4,
    "Congenital_myotonia|_autosomal_recessive_form|not_provided": 2,
    "not_specified|not_provided|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 3,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 544,
    "not_specified|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 9,
    "Inborn_genetic_diseases|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 7,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 370,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy|CLCN1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 4,
    "Congenital_myotonia|_autosomal_recessive_form|not_provided|Congenital_myotonia|_autosomal_dominant_form": 3,
    "not_specified|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Inborn_genetic_diseases": 1,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided": 68,
    "Batten-Turner_congenital_myopathy": 12,
    "not_provided|not_specified|CLCN1-related_disorder|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "Inborn_genetic_diseases|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 13,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Inborn_genetic_diseases": 3,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 43,
    "Inborn_genetic_diseases|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided": 6,
    "Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 13,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|Inborn_genetic_diseases|Batten-Turner_congenital_myopathy": 1,
    "not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 56,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Skeletal_muscle_channelopathy|not_provided": 1,
    "Congenital_myotonia|_autosomal_dominant_form": 22,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy": 4,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|RASopathy|not_provided": 1,
    "not_specified|not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 2,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified|Batten-Turner_congenital_myopathy": 2,
    "not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 30,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Inborn_genetic_diseases": 4,
    "not_specified|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_recessive_form|Tip-toe_gait|Congenital_myotonia|_autosomal_dominant_form|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy": 1,
    "not_provided|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified": 10,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|not_specified": 3,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy": 5,
    "not_provided|Congenital_myotonia|_autosomal_dominant_form": 3,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Tip-toe_gait": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|Batten-Turner_congenital_myopathy": 2,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "Inborn_genetic_diseases|Tip-toe_gait|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 1,
    "not_specified|not_provided|Batten-Turner_congenital_myopathy|CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "Tip-toe_gait|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 2,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Myotonia|Tip-toe_gait": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 2,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Inborn_genetic_diseases|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form": 1,
    "Rigidity|Myocardial_infarction|Myotonia_of_the_upper_limb|EMG:_myotonic_discharges|Headache|Vertigo|CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy": 3,
    "CLCN1-related_disorder|not_provided|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy": 2,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|not_provided|Congenital_myotonia|_autosomal_dominant_form": 2,
    "Batten-Turner_congenital_myopathy|not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 2,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified": 4,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 1,
    "Abnormality_of_the_musculature|Congenital_myotonia|_autosomal_recessive_form|not_provided|Congenital_myotonia|_autosomal_dominant_form": 1,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Batten-Turner_congenital_myopathy|not_provided": 3,
    "Batten-Turner_congenital_myopathy|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified": 1,
    "not_provided|not_specified|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 3,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified|not_provided": 3,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|Smith-Lemli-Opitz_syndrome|Tip-toe_gait": 1,
    "Myotonia|Batten-Turner_congenital_myopathy|CLCN1-related_disorder|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Abnormality_of_the_musculature|Congenital_myotonia|_autosomal_recessive_form|not_provided": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy|not_provided": 1,
    "Batten-Turner_congenital_myopathy|CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified": 1,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|Batten-Turner_congenital_myopathy": 3,
    "EMG:_myotonic_runs|Muscle_spasm|EMG:_neuropathic_changes|Memory_impairment|Migraine|Limb_pain|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Batten-Turner_congenital_myopathy": 1,
    "CLCN1-related_disorder": 7,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Metachromatic_leukodystrophy": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 2,
    "Myotonia|EMG:_myotonic_discharges|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 1,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|CLCN1-related_disorder": 2,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|CLCN1-related_disorder|not_specified": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Batten-Turner_congenital_myopathy": 1,
    "not_provided|CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 2,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Tip-toe_gait|not_provided|CLCN1-related_disorder": 1,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|CLCN1-related_disorder|not_provided": 1,
    "not_provided|Congenital_myotonia|_autosomal_recessive_form": 2,
    "not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified": 5,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified|not_provided|Batten-Turner_congenital_myopathy": 2,
    "not_specified|Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided": 1,
    "Autosomal_dominant_intermediate_Charcot-Marie-Tooth_disease|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|Batten-Turner_congenital_myopathy|Smith-Lemli-Opitz_syndrome|Tip-toe_gait": 1,
    "Congenital_myotonia|_autosomal_dominant_form|not_provided": 1,
    "Congenital_myotonia|_autosomal_dominant_form|not_provided|Congenital_myotonia|_autosomal_recessive_form": 2,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|CLCN1-related_disorder": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|not_provided": 1,
    "not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy": 3,
    "Batten-Turner_congenital_myopathy|Myotonia_levior|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 1,
    "Lumbar_hyperlordosis|Hypoplasia_of_the_maxilla|Skeletal_muscle_hypertrophy|Myotonia|Achilles_tendon_contracture": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 2,
    "not_specified|Batten-Turner_congenital_myopathy|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 2,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy|not_provided": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified|not_provided|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Batten-Turner_congenital_myopathy|not_provided|CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Batten-Turner_congenital_myopathy": 1,
    "Batten-Turner_congenital_myopathy|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified": 1,
    "Hyperkalemic_periodic_paralysis": 934,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Batten-Turner_congenital_myopathy": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_specified|Batten-Turner_congenital_myopathy": 1,
    "Inborn_genetic_diseases|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 2,
    "not_specified|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy": 1,
    "Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|not_provided|CLCN1-related_disorder|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Inborn_genetic_diseases": 1,
    "Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|CLCN1-related_disorder": 1,
    "not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form|Tip-toe_gait": 1,
    "Congenital_myotonia|_autosomal_recessive_form|not_specified": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy": 1,
    "Batten-Turner_congenital_myopathy|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form": 1,
    "CLCN1-related_disorder|not_provided": 1,
    "Myotonia|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided": 1,
    "Myopathy|EMG:_myopathic_abnormalities|CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Myotonia_levior|Congenital_myotonia|_autosomal_recessive_form|not_provided|Batten-Turner_congenital_myopathy|Cerebral_palsy|Tip-toe_gait|Abnormality_of_the_musculature": 1,
    "CLCN1-related_disorder|Abnormality_of_the_musculature|not_provided|Congenital_myotonia|_autosomal_recessive_form|Congenital_myotonia|_autosomal_dominant_form": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|Batten-Turner_congenital_myopathy": 1,
    "CLCN1-related_disorder|Congenital_myotonia|_autosomal_dominant_form|Congenital_myotonia|_autosomal_recessive_form|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Batten-Turner_congenital_myopathy": 1,
    "not_specified|Premature_ovarian_failure_5|not_provided": 2,
    "Premature_ovarian_failure_5": 40,
    "NOBOX-related_disorder": 9,
    "Inborn_genetic_diseases|not_provided|Premature_ovarian_failure_5": 1,
    "Premature_ovarian_failure_5|not_provided": 7,
    "not_provided|Premature_ovarian_failure_5": 6,
    "not_specified|not_provided|Premature_ovarian_failure_5": 4,
    "Premature_ovarian_failure_5|Inborn_genetic_diseases|not_provided": 1,
    "Premature_ovarian_failure_5|Inborn_genetic_diseases": 5,
    "Genetic_non-acquired_premature_ovarian_failure|not_provided|Premature_ovarian_failure_5": 1,
    "Inborn_genetic_diseases|Premature_ovarian_failure_5": 1,
    "not_provided|Premature_ovarian_failure_5|NOBOX-related_disorder": 1,
    "Premature_ovarian_failure_5|not_specified|Premature_ovarian_failure_1|not_provided": 1,
    "Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 181,
    "not_provided|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 13,
    "Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|Inborn_genetic_diseases": 3,
    "Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|not_specified": 1,
    "not_specified|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 2,
    "not_specified|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 2,
    "Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|not_provided": 6,
    "TPK1-related_disorder": 5,
    "Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|not_provided|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 6,
    "TPK1-related_disorder|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 1,
    "Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|TPK1-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 1,
    "TPK1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency": 1,
    "Inborn_genetic_diseases|Childhood_encephalopathy_due_to_thiamine_pyrophosphokinase_deficiency|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome": 891,
    "Pitt-Hopkins-like_syndrome|Cortical_dysplasia-focal_epilepsy_syndrome": 53,
    "Pitt-Hopkins-like_syndrome|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 10,
    "Pitt-Hopkins-like_syndrome|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified": 1,
    "not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 35,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome": 27,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified": 24,
    "not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 5,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases": 13,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified": 5,
    "CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome": 3,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 79,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome": 36,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_provided": 18,
    "Inborn_genetic_diseases|CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|not_provided|Intellectual_disability": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Pitt-Hopkins-like_syndrome": 12,
    "Inborn_genetic_diseases|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 15,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 73,
    "not_specified|not_provided|CNTNAP2-related_disorder|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 10,
    "CNTNAP2-related_disorder|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 3,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_specified": 3,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|CNTNAP2-related_disorder|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_provided|CNTNAP2-related_disorder": 1,
    "CNTNAP2-related_disorder": 4,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases": 30,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided": 5,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 13,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|Autism|_susceptibility_to|_15|not_specified|Pitt-Hopkins-like_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome": 4,
    "CNTNAP2-related_disorder|Intellectual_disability|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|not_provided": 4,
    "Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided": 1,
    "not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 4,
    "Focal-onset_seizure|Seizure|Hyperactivity|Gait_imbalance": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified": 7,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_specified|Pitt-Hopkins-like_syndrome|not_provided": 1,
    "not_specified|Pitt-Hopkins-like_syndrome|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Pitt-Hopkins-like_syndrome|Cortical_dysplasia-focal_epilepsy_syndrome": 10,
    "not_specified|CNTNAP2-related_disorder|not_provided|Inborn_genetic_diseases|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|not_provided|Inborn_genetic_diseases": 3,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|not_provided": 2,
    "Inborn_genetic_diseases|CNTNAP2-related_disorder|Pitt-Hopkins-like_syndrome|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Autism_spectrum_disorder|Intellectual_disability|Epilepsy|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 1,
    "Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 1,
    "Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|not_specified|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 3,
    "Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 2,
    "Inborn_genetic_diseases|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|CNTNAP2-related_disorder": 4,
    "Pitt-Hopkins-like_syndrome|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 2,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Inborn_genetic_diseases": 9,
    "CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "CNTNAP2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CNTNAP2-related_disorder|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 2,
    "CNTNAP2-related_disorder|Inborn_genetic_diseases|not_specified|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 2,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|CNTNAP2-related_disorder|not_specified|not_provided": 1,
    "Pitt-Hopkins-like_syndrome|CNTNAP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 2,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 3,
    "Inborn_genetic_diseases|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|See_cases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|CNTNAP2-related_disorder|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Pitt-Hopkins-like_syndrome|CNTNAP2-related_disorder|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 2,
    "Inborn_genetic_diseases|CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "CNTNAP2-related_disorder|not_provided|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_specified|CNTNAP2-related_disorder": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_specified|not_provided": 1,
    "Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_specified|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided|Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 4,
    "CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 2,
    "Cortical_dysplasia-focal_epilepsy_syndrome|CNTNAP2-related_disorder|not_specified": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|CNTNAP2-related_disorder": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 2,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_provided|not_specified": 2,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|Autism|_susceptibility_to|_15|CNTNAP2-related_disorder|not_specified": 1,
    "not_provided|CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided": 1,
    "CNTNAP2-related_disorder|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Self-limited_epilepsy_with_centrotemporal_spikes": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_specified": 3,
    "not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CNTNAP2-related_disorder|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome": 1,
    "Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_provided|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "CNTNAP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|See_cases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Self-limited_epilepsy_with_centrotemporal_spikes|not_specified|not_provided": 1,
    "not_provided|CNTNAP2-related_disorder|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Inborn_genetic_diseases|CNTNAP2-related_disorder": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Autism|_susceptibility_to|_15": 1,
    "Intellectual_disability|Cortical_dysplasia-focal_epilepsy_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|Inborn_genetic_diseases": 1,
    "Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|CNTNAP2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CNTNAP2-related_disorder|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases": 1,
    "CNTNAP2-related_disorder|Pitt-Hopkins-like_syndrome|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|Autism|_susceptibility_to|_15|not_provided": 1,
    "not_provided|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome": 2,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|not_specified": 2,
    "not_provided|Pitt-Hopkins-like_syndrome|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "CNTNAP2-related_disorder|Pitt-Hopkins-like_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "not_provided|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15|not_specified|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|not_specified|Autism|_susceptibility_to|_15|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|not_provided|CNTNAP2-related_disorder|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|CNTNAP2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_provided|Autism|_susceptibility_to|_15|not_specified": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|Pitt-Hopkins-like_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|Cortical_dysplasia-focal_epilepsy_syndrome": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_provided|Pitt-Hopkins-like_syndrome": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|Autism|_susceptibility_to|_15": 1,
    "not_specified|Inborn_genetic_diseases|Cortical_dysplasia-focal_epilepsy_syndrome|not_provided": 1,
    "not_specified|Cortical_dysplasia-focal_epilepsy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Cortical_dysplasia-focal_epilepsy_syndrome|Pitt-Hopkins-like_syndrome|not_provided": 1,
    "Weaver_syndrome": 403,
    "Weaver_syndrome|not_specified|not_provided": 3,
    "EZH2-related_disorder|not_provided|Weaver_syndrome": 2,
    "Weaver_syndrome|EZH2-related_disorder|not_provided": 2,
    "not_provided|Weaver_syndrome": 20,
    "not_provided|Weaver_syndrome|EZH2-related_disorder": 3,
    "not_specified|not_provided|Weaver_syndrome": 5,
    "Weaver_syndrome|not_provided": 17,
    "EZH2-related_disorder": 4,
    "Childhood_neoplasm|Hereditary_cancer-predisposing_syndrome": 2,
    "Weaver_syndrome|EZH2-related_disorder": 2,
    "not_specified|Weaver_syndrome|not_provided": 2,
    "Weaver_syndrome|not_provided|not_specified": 2,
    "EZH2-related_disorder|Weaver_syndrome": 1,
    "Weaver_syndrome|EZH2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Weaver_syndrome": 3,
    "Weaver_syndrome|Inborn_genetic_diseases": 3,
    "not_specified|Weaver_syndrome": 5,
    "Weaver_syndrome|EZH2-related_disorder|not_specified": 1,
    "not_provided|EZH2-related_disorder|Weaver_syndrome": 1,
    "EZH2-related_disorder|not_provided": 1,
    "Weaver_syndrome|Intellectual_disability|not_provided": 1,
    "Weaver_syndrome|not_provided|EZH2-related_disorder": 1,
    "Fetal_anomaly": 1,
    "EZH2-related_disorder|Weaver_syndrome|not_provided": 1,
    "Fibromatosis|_gingival|_6|Gingival_fibromatosis": 1,
    "Primary_Immune_Deficiency|not_provided": 1,
    "Portal_hypertension|_noncirrhotic|_2|Portal_hypertension": 1,
    "Portal_hypertension|Portal_hypertension|_noncirrhotic|_2": 2,
    "not_provided|Portal_hypertension|Portal_hypertension|_noncirrhotic|_2": 1,
    "Long_QT_syndrome_2": 88,
    "not_provided|Long_QT_syndrome_2": 8,
    "not_specified|not_provided|Cardiovascular_phenotype|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome": 104,
    "Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 8,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 8,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 25,
    "KCNH2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 36,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 4,
    "Long_QT_syndrome|not_provided|Short_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype": 36,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome": 13,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Short_QT_syndrome_type_1|Long_QT_syndrome_2|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia": 14,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 3,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome": 23,
    "Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome": 4,
    "Long_QT_syndrome|not_provided|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome": 16,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome": 4,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 1,
    "Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|Cardiac_arrhythmia|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome|Short_QT_syndrome_type_1|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_provided": 12,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 4,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|not_specified|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 5,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Congenital_long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|not_provided": 3,
    "KCNH2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "KCNH2-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiac_arrhythmia": 3,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 4,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 4,
    "Long_QT_syndrome|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 2,
    "Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome": 2,
    "not_specified|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 2,
    "Long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome_2": 1,
    "KCNH2-related_disorder|Torsades_de_pointes|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Sudden_unexplained_death": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Cardiac_arrhythmia|KCNH2-related_disorder|Congenital_long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_2": 7,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 6,
    "Cardiac_arrhythmia|not_provided|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|not_provided|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Long_QT_syndrome_2|Long_QT_syndrome": 5,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Long_QT_syndrome_2|Long_QT_syndrome|Short_QT_syndrome_type_1": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 34,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 5,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|not_specified": 1,
    "Long_QT_syndrome_2|not_provided|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 3,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 4,
    "not_provided|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 2,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 5,
    "not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 3,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_2": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|not_provided": 1,
    "Long_QT_syndrome|Long_QT_syndrome_2": 19,
    "not_specified|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_2|Long_QT_syndrome|Short_QT_syndrome_type_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 2,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 7,
    "Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 4,
    "Long_QT_syndrome|not_provided|Cardiac_arrhythmia": 7,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_2": 1,
    "KCNH2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|not_provided|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|not_provided|not_specified": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Long_QT_syndrome|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome_2|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome_1/2|_digenic|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_specified|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2": 5,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 6,
    "Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|not_provided": 4,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_1/2|_digenic|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 4,
    "Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Sudden_unexplained_death": 1,
    "Congenital_long_QT_syndrome|not_specified|Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|Short_QT_syndrome_type_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 3,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 2,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 2,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|not_provided": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|not_provided|KCNH2-related_disorder|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Long_QT_syndrome_2/9|_digenic": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|Long_QT_syndrome_2|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_specified": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|KCNH2-related_disorder": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 2,
    "not_specified|Long_QT_syndrome|not_provided": 4,
    "Atrial_fibrillation|not_specified|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_2|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_2|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 4,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia": 10,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Brugada_syndrome|KCNH2-related_disorder|not_specified|Long_QT_syndrome": 1,
    "KCNH2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Brugada_syndrome_1": 1,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia": 5,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_1/2|_digenic": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_2": 2,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 4,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_2/5|_digenic|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Long_QT_syndrome|KCNH2-related_disorder|Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome|Long_QT_syndrome_2|Congenital_long_QT_syndrome": 4,
    "Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 3,
    "Long_QT_syndrome|not_specified|Long_QT_syndrome_2": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 2,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Long_QT_syndrome_1": 1,
    "not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 4,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome_2|Long_QT_syndrome|not_provided": 1,
    "KCNH2-related_disorder": 3,
    "not_provided|Cardiac_arrhythmia|KCNH2-related_disorder": 1,
    "Cardiac_arrhythmia|not_specified|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Cardiac_arrhythmia|not_specified": 2,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_2": 2,
    "Long_QT_syndrome|Cardiac_arrhythmia|KCNH2-related_disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia|Long_QT_syndrome_2": 1,
    "KCNH2-related_disorder|not_provided|not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_1|not_specified|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "KCNH2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Brugada_syndrome|Long_QT_syndrome_2|Reclassified_-_variant_of_unknown_significance": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_2|not_provided": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome|not_specified": 1,
    "Acquired_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 5,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "not_provided|Congenital_long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome": 6,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided": 2,
    "not_specified|Long_QT_syndrome|not_provided|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_2|Long_QT_syndrome": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_specified": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Wolff-Parkinson-White_pattern": 1,
    "Sudden_cardiac_arrest": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome_2|Long_QT_syndrome": 3,
    "not_specified|Long_QT_syndrome|Cardiac_arrhythmia": 3,
    "Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2": 3,
    "Long_QT_syndrome_2|Congenital_long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_2|KCNH2-related_disorder|Congenital_long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|Long_QT_syndrome": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome|KCNH2-related_disorder|Cardiac_arrhythmia|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 8,
    "KCNH2-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "not_provided|Long_QT_syndrome_2|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Short_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome": 7,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_2": 6,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome|not_provided": 2,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Short_QT_syndrome_type_1|Congenital_long_QT_syndrome|Long_QT_syndrome_2": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome": 9,
    "not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2": 2,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Short_QT_syndrome": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome|Short_QT_syndrome_type_1": 1,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 6,
    "Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Cardiac_arrhythmia|Long_QT_syndrome_2|KCNH2-related_disorder|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_2": 1,
    "not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 3,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Autoimmune_lymphoproliferative_syndrome_due_to_CTLA4_haploinsufficiency|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 3,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia": 2,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Obesity|Prolonged_QT_interval": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2": 2,
    "Long_QT_syndrome_2|Long_QT_syndrome_1": 1,
    "not_specified|not_provided|Long_QT_syndrome_2|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_2|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Long_QT_syndrome_2|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_specified|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 5,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2|KCNH2-related_disorder|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome|_bradycardia-induced|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_2": 1,
    "KCNH2-related_disorder|not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome|KCNH2-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|not_specified": 1,
    "KCNH2-related_disorder|Long_QT_syndrome|not_provided": 1,
    "Cardiac_arrhythmia|Hypertrophic_cardiomyopathy": 2,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia|Cardiovascular_phenotype": 4,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_2|Long_QT_syndrome|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_2|not_specified": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "not_specified|Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 2,
    "Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome": 2,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome|not_specified": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Wolff-Parkinson-White_pattern|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome_2|not_provided": 3,
    "Long_QT_syndrome|Cardiovascular_phenotype|KCNH2-related_disorder|Cardiac_arrhythmia|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Brugada_syndrome_1|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Prolonged_QT_interval": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_2": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|not_specified|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|KCNH2-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_2|KCNH2-related_disorder|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_2|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 2,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Congenital_long_QT_syndrome|not_specified|Short_QT_syndrome_type_1": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_2": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Hypertrophic_cardiomyopathy|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|KCNH2-related_disorder|Long_QT_syndrome": 1,
    "Long_QT_syndrome|KCNH2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_2|not_specified": 1,
    "Long_QT_syndrome|Long_QT_syndrome_2|Cardiovascular_phenotype": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|not_provided|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2|KCNH2-related_disorder|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome_2|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|KCNH2-related_disorder|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|KCNH2-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|Short_QT_syndrome_type_1|not_provided|Long_QT_syndrome|Prolonged_QT_interval|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Long_QT_syndrome_2": 1,
    "Long_QT_syndrome|Long_QT_syndrome_2|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|Long_QT_syndrome|not_provided": 1,
    "Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "KCNH2-related_disorder|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiac_arrhythmia|Conduction_disorder_of_the_heart|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Long_QT_syndrome|KCNH2-related_disorder|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|KCNH2-related_disorder": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_2|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Long_QT_syndrome_2|Short_QT_syndrome_type_1": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided|Short_QT_syndrome_type_1": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_2/3|_digenic|Short_QT_syndrome_type_1|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_specified|not_provided": 2,
    "Congenital_long_QT_syndrome|Short_QT_syndrome_type_1": 3,
    "Long_QT_syndrome_2|Congenital_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "not_specified|Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1": 1,
    "not_provided|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Congenital_long_QT_syndrome": 1,
    "KCNH2-related_disorder|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_2|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Short_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_specified|Cardiac_arrhythmia": 1,
    "KCNH2-related_disorder|Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_1|Long_QT_syndrome_2|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome|KCNH2-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_2|Short_QT_syndrome_type_1|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "Cardiac_arrhythmia|Short_QT_syndrome_type_1|Long_QT_syndrome_2": 1,
    "CORONARY_ARTERY_SPASM_1|_SUSCEPTIBILITY_TO": 1,
    "Metabolic_syndrome|_susceptibility_to": 1,
    "NOS3-related_disorder": 9,
    "not_provided|NOS3-related_disorder": 3,
    "NOS3-related_disorder|not_provided": 7,
    "Preeclampsia/eclampsia_1|Ischemic_stroke|Alzheimer_disease_type_1|Essential_hypertension|_genetic|not_provided": 1,
    "Preeclampsia/eclampsia_1|Ischemic_stroke|Essential_hypertension|_genetic|Alzheimer_disease_type_1|not_specified|not_provided|CORONARY_ARTERY_SPASM_1|_SUSCEPTIBILITY_TO": 1,
    "NOS3-related_disorder|not_provided|not_specified": 1,
    "Alzheimer_disease_type_1": 6,
    "not_provided|not_specified|NOS3-related_disorder": 1,
    "CDK5-related_disorder": 3,
    "Lissencephaly_7_with_cerebellar_hypoplasia": 2,
    "Osteopetrosis|_autosomal_recessive_9": 2,
    "Osteopetrosis|_autosomal_recessive_9|not_specified": 1,
    "Glaucoma_1|_open_angle|_F": 29,
    "Glaucoma_1|_open_angle|_F|not_provided": 10,
    "ASB10-related_disorder": 3,
    "ASB10-related_disorder|not_provided": 2,
    "Glaucoma_1|_open_angle|_F|not_specified": 3,
    "not_provided|Glaucoma_1|_open_angle|_F": 9,
    "not_provided|Glaucoma_1|_open_angle|_F|not_specified": 1,
    "not_provided|ASB10-related_disorder|Glaucoma_1|_open_angle|_F": 1,
    "not_provided|ASB10-related_disorder": 2,
    "RHEB-related_disorder|not_provided": 1,
    "Hemimegalencephaly": 5,
    "Seizure|Neurodevelopmental_delay": 1,
    "Wolff-Parkinson-White_pattern|not_provided|Hypertrophic_cardiomyopathy_6": 6,
    "Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern": 10,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern": 9,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern": 2,
    "Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_provided": 2,
    "Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6": 9,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided": 1,
    "Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_provided": 3,
    "not_provided|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern": 4,
    "not_provided|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6": 2,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 25,
    "not_specified|PRKAG2-related_disorder|Cardiomyopathy": 1,
    "not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern": 1,
    "Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart": 348,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 4,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 2,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Wolff-Parkinson-White_pattern": 1,
    "Cardiomyopathy|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 22,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart": 11,
    "not_provided|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|PRKAG2-related_disorder": 2,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 17,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 1,
    "PRKAG2-related_disorder": 8,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 4,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 9,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 19,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_6|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_specified|Wolff-Parkinson-White_pattern": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|not_provided": 1,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 2,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Wolff-Parkinson-White_syndrome|_childhood-onset|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 23,
    "Cardiovascular_phenotype|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|not_provided": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 9,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 19,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 2,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_6": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_specified": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 2,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided": 5,
    "Hypertrophic_cardiomyopathy_6": 9,
    "not_provided|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified": 11,
    "not_specified|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Wolff-Parkinson-White_pattern|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_hypertrophy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 3,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_specified|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|not_provided|PRKAG2-related_disorder": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_specified": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 25,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 5,
    "Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 2,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 2,
    "Hypertrophic_cardiomyopathy|PRKAG2-related_disorder|Hypertrophic_cardiomyopathy_6": 1,
    "not_provided|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Wolff-Parkinson-White_pattern": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|not_specified": 2,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|not_provided|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_specified": 1,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_provided|Cardiomyopathy|Wolff-Parkinson-White_pattern": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Wolff-Parkinson-White_pattern": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 2,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy": 5,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 3,
    "PRKAG2_syndrome": 1,
    "not_specified|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "PRKAG2-related_disorder|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 5,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Cardiomyopathy": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|not_provided|not_specified|Cardiomyopathy": 1,
    "PRKAG2-related_cardiomyopathy": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Wolff-Parkinson-White_pattern|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|PRKAG2-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart": 2,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 7,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "PRKAG2-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_specified|Cardiomyopathy|not_provided": 1,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_provided": 1,
    "Cardiomyopathy|PRKAG2-related_disorder|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 55,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome": 2,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiomyopathy|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "PRKAG2-related_disorder|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype": 1,
    "Wolff-Parkinson-White_pattern|Cardiovascular_phenotype": 1,
    "Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiomyopathy": 2,
    "not_provided|PRKAG2-related_disorder": 1,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|PRKAG2-related_disorder|not_specified": 1,
    "Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 3,
    "not_specified|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_provided|See_cases|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiovascular_phenotype": 4,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 23,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 2,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|PRKAG2-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|PRKAG2_cardiac_syndrome|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertensive_disorder|Stroke_disorder|Ventricular_tachycardia|Webbed_neck|Coronary_artery_disorder|Left_ventricular_hypertrophy|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 2,
    "Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 2,
    "Hypertrophic_cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Wolff-Parkinson-White_pattern|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_specified|Wolff-Parkinson-White_pattern|Cardiomyopathy": 1,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_specified|PRKAG2-related_disorder": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "PRKAG2-related_disorder|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_specified|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy": 1,
    "Congestive_heart_failure|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Hypertrophic_cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Hypertrophic_cardiomyopathy|Cardiomyopathy|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype": 1,
    "PRKAG2-related_disorder|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy": 1,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_specified|PRKAG2-related_disorder|Cardiomyopathy|Wolff-Parkinson-White_pattern|not_provided": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|PRKAG2_cardiac_syndrome|Renal_cysts_and_diabetes_syndrome|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "PRKAG2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|not_provided|Heart_failure|Hypertrophic_cardiomyopathy|Wolff-Parkinson-White_pattern": 1,
    "not_specified|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|PRKAG2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Wolff-Parkinson-White_pattern|not_specified": 1,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_specified|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided|PRKAG2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|PRKAG2-related_disorder|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|PRKAG2-related_disorder|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|PRKAG2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_6|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "not_provided|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|not_provided|Cardiomyopathy|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_6|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|not_specified|not_provided|Wolff-Parkinson-White_pattern|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_6|Cardiomyopathy|PRKAG2-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart|Hypertrophic_cardiomyopathy_6|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|not_specified|Wolff-Parkinson-White_pattern": 1,
    "Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Lethal_congenital_glycogen_storage_disease_of_heart|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6": 1,
    "Lethal_congenital_glycogen_storage_disease_of_heart|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy_6|not_specified|not_provided": 1,
    "not_provided|Wolff-Parkinson-White_pattern|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Lethal_congenital_glycogen_storage_disease_of_heart": 2,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Wolff-Parkinson-White_pattern|Lethal_congenital_glycogen_storage_disease_of_heart": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided|Wolff-Parkinson-White_pattern": 2,
    "GALNTL5-related_disorder": 3,
    "GALNTL5-related_disorder|not_provided": 1,
    "not_provided|GALNTL5-related_disorder": 1,
    "not_specified|GALNTL5-related_disorder": 1,
    "GALNT11-related_disorder|not_provided": 1,
    "Kleefstra_syndrome_2": 191,
    "not_provided|Kleefstra_syndrome_2": 18,
    "Kleefstra_syndrome_2|not_provided": 23,
    "KMT2C-related_disorder": 45,
    "KMT2C-related_NDD": 52,
    "KMT2C-related_disorder|not_provided": 27,
    "KMT2C-related_NDD|not_provided": 5,
    "KMT2C-related_disorder|Kleefstra_syndrome_2": 2,
    "Microcephaly|KMT2C-related_NDD|not_provided": 1,
    "Kleefstra_syndrome_2|not_specified|not_provided": 3,
    "not_provided|KMT2C-related_disorder": 18,
    "KMT2C-related_disorder|not_provided|not_specified": 2,
    "not_provided|Kleefstra_syndrome_2|Inborn_genetic_diseases": 3,
    "KMT2C-related_disorder|Tip-toe_gait|not_provided": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_2": 3,
    "not_provided|KMT2C-related_disorder|KMT2C-related_NDD": 1,
    "KMT2C-related_disorder|not_specified": 1,
    "KMT2C-related_disorder|Kleefstra_syndrome_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KMT2C-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_2|KMT2C-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Tip-toe_gait": 1,
    "Kleefstra_syndrome_2|not_specified": 3,
    "KMT2C-related_disorder|Inborn_genetic_diseases": 2,
    "Tip-toe_gait|Kleefstra_syndrome_2|not_provided": 1,
    "KMT2C-related_NDD|Kleefstra_syndrome_2": 6,
    "Kleefstra_syndrome_2|Inborn_genetic_diseases": 7,
    "not_specified|KMT2C-related_disorder|not_provided|Kleefstra_syndrome_2": 1,
    "not_provided|KMT2C-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|KMT2C-related_disorder": 1,
    "not_provided|not_specified|Kleefstra_syndrome_2": 2,
    "KMT2C-related_disorder|not_specified|not_provided": 9,
    "KMT2C-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "KMT2C-related_disorder|Kleefstra_syndrome_2|not_specified|not_provided|Intellectual_disability": 1,
    "Kleefstra_syndrome": 3,
    "not_specified|KMT2C-related_disorder|not_provided": 1,
    "not_specified|Kleefstra_syndrome_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KMT2C-related_disorder": 1,
    "not_provided|KMT2C-related_disorder|See_cases": 1,
    "KMT2C-related_NDD|Rare_genetic_intellectual_disability|Kleefstra_syndrome_2": 1,
    "Neurodevelopmental_abnormality|Autism_spectrum_disorder": 1,
    "Kleefstra_syndrome_1|KMT2C-related_NDD|Kleefstra_syndrome_2": 1,
    "atypical_cerebral_palsy|KMT2C-related_disorder|not_specified|not_provided": 1,
    "not_specified|KMT2C-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|KMT2C-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|KMT2C-related_disorder": 2,
    "Kleefstra_syndrome_2|Neurodevelopmental_disorder|not_provided": 1,
    "not_specified|not_provided|KMT2C-related_disorder": 1,
    "Kleefstra_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|KMT2C-related_disorder": 1,
    "Neurodevelopmental_delay|Kleefstra_syndrome_2": 1,
    "Kleefstra_syndrome_2|not_provided|KMT2C-related_disorder": 2,
    "not_specified|not_provided|KMT2C-related_disorder|Inborn_genetic_diseases": 1,
    "See_cases|KMT2C-related_disorder|not_provided": 1,
    "not_provided|Kleefstra_syndrome_2|not_specified": 2,
    "KMT2C-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Tip-toe_gait|not_specified|Syndromic_intellectual_disability": 1,
    "not_provided|KMT2C-related_NDD": 3,
    "not_provided|Inborn_genetic_diseases|Kleefstra_syndrome_2": 2,
    "Kleefstra_syndrome_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Kleefstra_syndrome_2|KMT2C-related_disorder": 2,
    "Kleefstra_syndrome_2|See_cases": 1,
    "Kleefstra_syndrome_2|KMT2C-related_NDD|not_provided": 1,
    "Kleefstra_syndrome_due_to_a_point_mutation|KMT2C-related_NDD": 1,
    "Kleefstra_syndrome_2|Intellectual_disability": 1,
    "Global_developmental_delay|Cerebellar_atrophy|Kleefstra_syndrome_2": 1,
    "Kleefstra_syndrome_2|not_specified|Autism|_susceptiblity_to": 1,
    "not_specified|Kleefstra_syndrome_2": 1,
    "not_specified|not_provided|Kleefstra_syndrome_2": 1,
    "Syndromic_intellectual_disability|KMT2C-related_NDD": 1,
    "Premature_ovarian_failure_17|Fanconi_anemia_complementation_group_U|Spermatogenic_failure_50|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "XRCC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|XRCC2-related_disorder|not_specified|Fanconi_anemia_complementation_group_U|not_provided": 1,
    "Fanconi_anemia_complementation_group_U": 2,
    "Hereditary_cancer-predisposing_syndrome|Spermatogenic_failure_50|Premature_ovarian_failure_17|Fanconi_anemia_complementation_group_U|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|XRCC2-related_disorder|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 145,
    "Fanconi_anemia_complementation_group_U|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_provided|Fanconi_anemia_complementation_group_U|Hereditary_cancer-predisposing_syndrome": 3,
    "XRCC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Spermatogenic_failure_50|Premature_ovarian_failure_17|Fanconi_anemia_complementation_group_U|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_U": 1,
    "Spermatogenic_failure_50|Premature_ovarian_failure_17|Fanconi_anemia_complementation_group_U|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_U|not_provided": 2,
    "Fanconi_anemia_complementation_group_U|not_provided|Hereditary_cancer-predisposing_syndrome|Short_stature|_microcephaly|_and_endocrine_dysfunction": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Fanconi_anemia_complementation_group_U|Colon_cancer": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_U": 2,
    "not_provided|Spermatogenic_failure_50|Premature_ovarian_failure_17|Fanconi_anemia_complementation_group_U|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|XRCC2-related_disorder": 1,
    "Spermatogenic_failure_50|Fanconi_anemia_complementation_group_U|Premature_ovarian_failure_17": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|XRCC2-related_disorder": 1,
    "XRCC2-related_disorder": 1,
    "XRCC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Fanconi_anemia_complementation_group_U|Spermatogenic_failure_50|Premature_ovarian_failure_17|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_U|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|XRCC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Fanconi_anemia_complementation_group_U|Spermatogenic_failure_50|Premature_ovarian_failure_17|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_U|not_provided": 1,
    "Spermatogenic_failure_50|Premature_ovarian_failure_17|Fanconi_anemia_complementation_group_U|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|XRCC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_U": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|XRCC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_carcinoma": 1,
    "XRCC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Premature_ovarian_failure_17|Spermatogenic_failure_50|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_U|not_provided|not_specified": 1,
    "Fanconi_anemia_complementation_group_U|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Fanconi_anemia_complementation_group_U": 1,
    "Intellectual_disability|_autosomal_dominant_33": 19,
    "DPP6-related_disorder": 25,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_33|Ventricular_fibrillation|_paroxysmal_familial|_2": 2,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_2": 1,
    "HP:0000729_Autistic_spectrum_disorder": 1,
    "not_provided|DPP6-related_disorder": 3,
    "Intellectual_disability|_autosomal_dominant_33|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_33|not_provided": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_2|Intellectual_disability|_autosomal_dominant_33|Complex_neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_33|Ventricular_fibrillation|_paroxysmal_familial|_2|not_specified|not_provided": 1,
    "DPP6-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_33|Ventricular_fibrillation|_paroxysmal_familial|_2": 1,
    "DPP6-related_disorder|not_provided": 4,
    "Intellectual_disability|_autosomal_dominant_33|Ventricular_fibrillation|_paroxysmal_familial|_2": 2,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_2|Intellectual_disability|_autosomal_dominant_33": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_2": 1,
    "DPP6-related_disorder|not_provided|not_specified": 1,
    "Collapse_(finding)|Ventricular_tachycardia": 1,
    "Autism|_susceptibility_to|_10": 2,
    "not_specified|SHH-related_disorder": 1,
    "Partial_agenesis_of_the_corpus_callosum": 2,
    "SHH-related_disorder": 23,
    "not_provided|SHH-related_disorder": 5,
    "Inborn_genetic_diseases|SHH-related_disorder|not_provided": 1,
    "Holoprosencephaly_3": 327,
    "Inborn_genetic_diseases|Holoprosencephaly_3": 6,
    "Holoprosencephaly_3|not_provided": 15,
    "Holoprosencephaly_3|SHH-related_disorder": 7,
    "Acrocallosal_syndrome": 813,
    "not_specified|SHH-related_disorder|not_provided": 1,
    "Microphthalmia|_isolated|_with_coloboma_5|Holoprosencephaly_3": 1,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_3": 2,
    "SHH-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_3|SHH-related_disorder": 1,
    "Inborn_genetic_diseases|Solitary_median_maxillary_central_incisor_syndrome|Holoprosencephaly_3|Microphthalmia|_isolated|_with_coloboma_5|Schizencephaly|not_provided": 1,
    "not_provided|Holoprosencephaly_3": 8,
    "not_provided|Microphthalmia|_isolated|_with_coloboma_5|Schizencephaly|Solitary_median_maxillary_central_incisor_syndrome|Holoprosencephaly_3": 1,
    "Solitary_median_maxillary_central_incisor_syndrome": 21,
    "Microphthalmia|_isolated|_with_coloboma_5": 1,
    "SHH-related_disorder|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Holoprosencephaly_3": 1,
    "Holoprosencephaly_3|SHH-related_disorder|not_provided|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "Inborn_genetic_diseases|SHH-related_disorder": 1,
    "Holoprosencephaly_3|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Holoprosencephaly_3": 1,
    "Solitary_median_maxillary_central_incisor_syndrome|Holoprosencephaly_3|Schizencephaly|Microphthalmia|_isolated|_with_coloboma_5": 1,
    "Holoprosencephaly_3|not_specified|not_provided": 2,
    "SHH-related_disorder|Microphthalmia|_isolated|_with_coloboma_5|Schizencephaly|Solitary_median_maxillary_central_incisor_syndrome|Holoprosencephaly_3|not_specified|not_provided": 1,
    "Holoprosencephaly_3|Inborn_genetic_diseases": 4,
    "Holoprosencephaly_3|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "SHH-related_disorder|Holoprosencephaly_3": 2,
    "Holoprosencephaly_3|SHH-related_disorder|not_provided": 1,
    "Solitary_median_maxillary_central_incisor_syndrome|SHH-related_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_provided|Holoprosencephaly_3": 1,
    "not_provided|not_specified|Holoprosencephaly_3": 1,
    "not_provided|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "not_provided|SHH-related_disorder|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "Solitary_median_maxillary_central_incisor_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_3|not_specified": 1,
    "not_specified|Holoprosencephaly_3": 1,
    "not_provided|Holoprosencephaly_3|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "Holoprosencephaly_3|Solitary_median_maxillary_central_incisor_syndrome|Microphthalmia|_isolated|_with_coloboma_5|not_specified|not_provided": 1,
    "Holoprosencephaly_3|not_provided|not_specified|Schizencephaly|Microphthalmia|_isolated|_with_coloboma_5|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "Holoprosencephaly_3|Microphthalmia|_isolated|_with_coloboma_5|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "Holoprosencephaly_3|Developmental_and_epileptic_encephalopathy|_11": 1,
    "SHH-related_disorder|Holoprosencephaly_3|not_provided": 1,
    "not_provided|Holoprosencephaly_3|SHH-related_disorder|not_specified": 1,
    "Macrotia|Axial_hypotonia|Diarrhea|High_palate|Anemia|Elevated_circulating_aspartate_aminotransferase_concentration|Failure_to_thrive|Moderate_global_developmental_delay|Elevated_circulating_alanine_aminotransferase_concentration|Vomiting": 1,
    "Microphthalmia|_isolated|_with_coloboma_5|Holoprosencephaly_3|Solitary_median_maxillary_central_incisor_syndrome": 1,
    "not_provided|Holoprosencephaly_3|not_specified": 1,
    "Polydactyly_of_a_triphalangeal_thumb": 86,
    "not_provided|Polydactyly_of_a_triphalangeal_thumb": 16,
    "Triphalangeal_thumb-polysyndactyly_syndrome": 3,
    "Polydactyly_of_a_triphalangeal_thumb|not_provided": 10,
    "Triphalangeal_thumb-polysyndactyly_syndrome|not_provided": 2,
    "Polydactyly_of_a_triphalangeal_thumb|Syndactyly_type_4|Acheiropodia|Laurin-Sandrow_syndrome|Triphalangeal_thumb-polysyndactyly_syndrome": 1,
    "Congenital_limb_malformation": 1,
    "Syndactyly_type_4|Acheiropodia|Laurin-Sandrow_syndrome|Triphalangeal_thumb-polysyndactyly_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Polydactyly_of_a_triphalangeal_thumb": 1,
    "LMBR1-related_disorder": 11,
    "LMBR1-related_disorder|Inborn_genetic_diseases": 1,
    "Laurin-Sandrow_syndrome|Triphalangeal_thumb-polysyndactyly_syndrome|Syndactyly_type_4|Acheiropodia": 1,
    "not_specified|not_provided|Polydactyly_of_a_triphalangeal_thumb": 1,
    "Acheiropodia|Laurin-Sandrow_syndrome|Triphalangeal_thumb-polysyndactyly_syndrome|Syndactyly_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Polydactyly_of_a_triphalangeal_thumb|LMBR1-related_disorder": 1,
    "Triphalangeal_thumb|Polydactyly_of_a_triphalangeal_thumb|not_provided": 1,
    "Triphalangeal_thumb|Polydactyly_of_a_triphalangeal_thumb": 2,
    "SHH-related_disorder|not_provided": 1,
    "Syndactyly_type_4|Tibia|_hypoplasia_or_aplasia_of|_with_polydactyly|Acheiropodia|Laurin-Sandrow_syndrome|Polydactyly_of_a_triphalangeal_thumb|Triphalangeal_thumb-polysyndactyly_syndrome|not_provided": 1,
    "Tibia|_hypoplasia_or_aplasia_of|_with_polydactyly": 2,
    "not_provided|Triphalangeal_thumb|Polydactyly_of_a_triphalangeal_thumb|Tibia|_hypoplasia_or_aplasia_of|_with_polydactyly": 1,
    "Polydactyly_of_a_triphalangeal_thumb|Triphalangeal_thumb|not_provided": 1,
    "Inborn_genetic_diseases|Polydactyly_of_a_triphalangeal_thumb|not_provided": 1,
    "Inborn_genetic_diseases|Skeletal_dysplasia|Polydactyly_of_a_triphalangeal_thumb|not_provided": 1,
    "not_provided|Triphalangeal_thumb-polysyndactyly_syndrome": 1,
    "MNX1-related_disorder": 13,
    "Currarino_triad": 52,
    "Abnormality_of_the_vertebral_column|MNX1-related_disorder": 1,
    "not_provided|Currarino_triad": 24,
    "Currarino_triad|not_provided": 12,
    "Currarino_triad|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Currarino_triad": 3,
    "MNX1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Currarino_triad|not_provided": 1,
    "Inborn_genetic_diseases|Currarino_triad|not_provided": 1,
    "not_provided|Currarino_triad|Inborn_genetic_diseases": 1,
    "MNX1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Currarino_triad": 1,
    "Currarino_triad|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Currarino_triad": 2,
    "not_provided|MNX1-related_disorder": 1,
    "Currarino_triad|MNX1-related_disorder|not_provided": 1,
    "UBE3C-related_disorder": 8,
    "Neurodevelopmental_disorder_with_absent_speech_and_movement_and_behavioral_abnormalities": 1,
    "See_cases|Neurodevelopmental_disorder_with_absent_speech_and_movement_and_behavioral_abnormalities": 1,
    "not_provided|UBE3C-related_disorder": 1,
    "Myofibrillar_Myopathy|_Dominant|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 13,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 10,
    "Myofibrillar_Myopathy|_Dominant|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 3,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 258,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided": 18,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|not_provided|not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|DNAJB6-related_disorder": 1,
    "not_specified|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|DNAJB6-related_disorder": 1,
    "Inborn_genetic_diseases|DNAJB6-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 25,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 4,
    "not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 5,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided|not_specified": 2,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|Proximal_muscle_weakness|Muscle_weakness": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|Abnormality_of_the_musculature|not_provided": 1,
    "Myofibrillar_Myopathy|_Dominant|not_specified|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "DNAJB6-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 6,
    "Inborn_genetic_diseases|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 8,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_specified|not_provided": 3,
    "not_provided|DNAJB6-related_disorder|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|Inborn_genetic_diseases": 3,
    "not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided": 1,
    "Myofibrillar_Myopathy|_Dominant|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|Inborn_genetic_diseases": 1,
    "Parkinson_disease|_late-onset|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant|not_provided|Inborn_genetic_diseases|not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "not_specified|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 3,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_specified": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Limb-Girdle_Muscular_Dystrophy|_Dominant|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided|Limb-Girdle_Muscular_Dystrophy|_Dominant|not_specified": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|Muscular_dystrophy|_limb-girdle|_autosomal_dominant|not_provided": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|not_specified|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "DNAJB6-related_disorder|Limb-Girdle_Muscular_Dystrophy|_Dominant|Myofibrillar_Myopathy|_Dominant|not_specified|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 1,
    "Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided|Myofibrillar_Myopathy|_Dominant": 3,
    "Myofibrillar_Myopathy|_Dominant|Limb-Girdle_Muscular_Dystrophy|_Dominant": 1,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|not_provided|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)": 2,
    "Limb-Girdle_Muscular_Dystrophy|_Dominant|Autosomal_dominant_limb-girdle_muscular_dystrophy_type_1D_(DNAJB6)|not_provided": 1,
    "NCAPG2-related_disorder": 13,
    "NCAPG2-related_disorder|not_provided": 11,
    "not_provided|Khan-Khan-Katsanis_syndrome": 4,
    "not_provided|NCAPG2-related_disorder": 3,
    "Khan-Khan-Katsanis_syndrome": 15,
    "NCAPG2-related_disorder|not_provided|Khan-Khan-Katsanis_syndrome|not_specified": 1,
    "NCAPG2-related_disorder|not_provided|not_specified": 1,
    "NCAPG2-related_disorder|not_specified": 1,
    "not_specified|NCAPG2-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 314,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|Inborn_genetic_diseases": 22,
    "not_specified|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 26,
    "not_provided|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 10,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|Inborn_genetic_diseases|DYNC2I1-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_provided": 12,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|DYNC2I1-related_disorder|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 1,
    "not_provided|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_specified": 2,
    "DYNC2I1-related_disorder": 6,
    "not_specified|not_provided|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 4,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_provided|DYNC2I1-related_disorder": 1,
    "DYNC2I1-related_disorder|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 7,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 2,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_provided|DYNC2I1-related_disorder": 2,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|See_cases": 1,
    "Cystic_renal_disease": 1,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|not_provided|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|DYNC2I1-related_disorder": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|DYNC2I1-related_disorder|not_provided": 1,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|DYNC2I1-related_disorder": 4,
    "Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|Asphyxiating_thoracic_dystrophy_3": 1,
    "See_cases|Asphyxiating_thoracic_dystrophy_3|DYNC2I1-related_disorder|Jeune_thoracic_dystrophy|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 1,
    "not_provided|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly|DYNC2I1-related_disorder": 2,
    "Asphyxiating_thoracic_dystrophy_3": 238,
    "Asphyxiating_thoracic_dystrophy_3|Short-rib_thoracic_dysplasia_8_with_or_without_polydactyly": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 86,
    "DLGAP2-related_disorder": 24,
    "not_specified|DLGAP2-related_disorder": 1,
    "DLGAP2-related_disorder|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_8": 46,
    "not_specified|Neuronal_ceroid_lipofuscinosis": 58,
    "not_specified|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8": 3,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_8": 3,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_specified|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis": 115,
    "Neuronal_ceroid_lipofuscinosis_8|not_provided|Neuronal_ceroid_lipofuscinosis": 4,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8": 19,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 19,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 57,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|not_specified|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_8|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Intellectual_disability|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 3,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 35,
    "not_provided|Neuronal_ceroid_lipofuscinosis_8": 3,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_8|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 19,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided": 5,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_8": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_1": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 3,
    "not_specified|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases": 2,
    "Neuronal_ceroid_lipofuscinosis_8|not_specified|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8": 5,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases|CLN8-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "CLN8-related_disorder|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided": 53,
    "Neuronal_ceroid_lipofuscinosis_8|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "CLN8-related_disorder|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8|Intellectual_disability|not_specified|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 6,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 1,
    "CLN8-related_disorder|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_8|not_specified|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_8|Inborn_genetic_diseases": 1,
    "not_provided|CLN8-related_disorder|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|CLN8-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|not_provided|Neuronal_ceroid_lipofuscinosis_8": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8": 1,
    "Intellectual_disability|Neuronal_ceroid_lipofuscinosis|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified": 58,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8": 1,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|not_provided|CLN8-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_8|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8": 1,
    "Neuronal_ceroid_lipofuscinosis_8|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_8|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|CLN8-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Central_core_myopathy|Neuronal_ceroid_lipofuscinosis_8": 1,
    "Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8": 1,
    "not_provided|CLN8-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_specified": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_specified|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_8|not_provided": 1,
    "CLN8-related_disorder|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis_8|not_provided|Neuronal_ceroid_lipofuscinosis|See_cases": 1,
    "Neuronal_ceroid_lipofuscinosis_8|Inborn_genetic_diseases": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 4,
    "Neuronal_ceroid_lipofuscinosis_8|Neuronal_ceroid_lipofuscinosis_8_northern_epilepsy_variant|Neuronal_ceroid_lipofuscinosis": 1,
    "ARHGEF10-related_disorder": 6,
    "not_provided|ARHGEF10-related_disorder": 12,
    "not_specified|not_provided|Autosomal_dominant_slowed_nerve_conduction_velocity": 4,
    "Autosomal_dominant_slowed_nerve_conduction_velocity": 17,
    "not_provided|ARHGEF10-related_disorder|Autosomal_dominant_slowed_nerve_conduction_velocity|not_specified": 1,
    "not_provided|not_specified|Autosomal_dominant_slowed_nerve_conduction_velocity": 2,
    "not_provided|Autosomal_dominant_slowed_nerve_conduction_velocity": 7,
    "ARHGEF10-related_disorder|not_provided": 2,
    "ARHGEF10-related_disorder|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_dominant_slowed_nerve_conduction_velocity": 2,
    "not_specified|Autosomal_dominant_slowed_nerve_conduction_velocity|not_provided": 4,
    "Autosomal_dominant_slowed_nerve_conduction_velocity|Myopathy|Spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease|Autosomal_dominant_slowed_nerve_conduction_velocity|ARHGEF10-related_disorder|not_provided": 1,
    "Autosomal_dominant_slowed_nerve_conduction_velocity|ARHGEF10-related_disorder|not_provided": 1,
    "not_provided|ARHGEF10-related_disorder|not_specified": 1,
    "Autosomal_dominant_slowed_nerve_conduction_velocity|not_specified": 1,
    "Autosomal_dominant_slowed_nerve_conduction_velocity|ARHGEF10-related_disorder|not_specified|not_provided": 1,
    "not_specified|Autosomal_dominant_slowed_nerve_conduction_velocity": 1,
    "Autosomal_dominant_slowed_nerve_conduction_velocity|not_provided": 3,
    "Autosomal_dominant_slowed_nerve_conduction_velocity|not_specified|not_provided": 1,
    "not_specified|ARHGEF10-related_disorder|not_provided": 2,
    "not_specified|ARHGEF10-related_disorder": 1,
    "MYOM2-related_disorder": 99,
    "not_provided|MYOM2-related_disorder": 8,
    "not_specified|MYOM2-related_disorder": 3,
    "CSMD1-related_disorder": 71,
    "not_provided|CSMD1-related_disorder": 11,
    "CSMD1-related_disorder|not_specified": 4,
    "not_specified|CSMD1-related_disorder": 6,
    "CSMD1-related_disorder|not_provided": 12,
    "Cerebellar_ataxia|not_provided|not_specified|CSMD1-related_disorder": 1,
    "Small_for_gestational_age|Normal_pregnancy|Gestational_diabetes_mellitus_uncontrolled|Large_for_gestational_age": 1,
    "Gestational_diabetes_mellitus_uncontrolled|Normal_pregnancy": 1,
    "Primary_Microcephaly|_Recessive|not_provided": 3,
    "MCPH1-related_disorder": 4,
    "not_specified|not_provided|Microcephaly_1|_primary|_autosomal_recessive": 6,
    "Microcephaly_1|_primary|_autosomal_recessive|not_specified|not_provided": 12,
    "not_provided|Microcephaly_1|_primary|_autosomal_recessive": 28,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided": 22,
    "not_provided|MCPH1-related_disorder": 7,
    "MCPH1-related_disorder|Microcephaly_1|_primary|_autosomal_recessive|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Microcephaly_1|_primary|_autosomal_recessive|Microcephaly": 1,
    "not_specified|Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder|not_provided": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder|not_provided": 2,
    "Autosomal_recessive_primary_microcephaly|Microcephaly_1|_primary|_autosomal_recessive|See_cases": 1,
    "not_specified|Microcephaly_1|_primary|_autosomal_recessive|not_provided": 4,
    "MCPH1-related_disorder|not_provided": 6,
    "not_specified|MCPH1-related_disorder|not_provided": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided|Abnormality_of_the_nervous_system": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|Inborn_genetic_diseases": 10,
    "Abnormal_brain_morphology|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "MCPH1-related_disorder|not_specified|not_provided|Microcephaly_1|_primary|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|MCPH1-related_disorder|not_provided": 1,
    "MCPH1-related_disorder|Microcephaly_1|_primary|_autosomal_recessive|not_provided": 2,
    "not_provided|Microcephaly_1|_primary|_autosomal_recessive|not_specified|MCPH1-related_disorder": 2,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 6,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided|not_specified|MCPH1-related_disorder": 1,
    "not_provided|Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|MCPH1-related_disorder": 1,
    "not_provided|Autosomal_recessive_primary_microcephaly": 1,
    "not_specified|not_provided|Microcephaly_1|_primary|_autosomal_recessive|Intellectual_disability": 1,
    "not_specified|not_provided|Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided|not_specified": 7,
    "Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|MCPH1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 3,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases|MCPH1-related_disorder": 1,
    "not_provided|Microcephaly_1|_primary|_autosomal_recessive|not_specified": 6,
    "MCPH1-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_primary_microcephaly|not_provided|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Microcephaly_1|_primary|_autosomal_recessive|not_provided|not_specified": 1,
    "Autosomal_recessive_primary_microcephaly|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly_1|_primary|_autosomal_recessive": 2,
    "not_provided|Microcephaly_1|_primary|_autosomal_recessive|Autosomal_recessive_primary_microcephaly": 1,
    "Autosomal_recessive_primary_microcephaly|Microcephaly_1|_primary|_autosomal_recessive|not_provided|MCPH1-related_disorder|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_1|_primary|_autosomal_recessive|Intellectual_disability|Short_stature": 1,
    "Lymphatic_malformation_10": 3,
    "ANGPT2-related_disorder": 2,
    "not_specified|not_provided|MCPH1-related_disorder": 1,
    "MCPH1-related_disorder|not_provided|not_specified": 1,
    "Intellectual_disability|not_provided|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Microcephaly_1|_primary|_autosomal_recessive|not_provided": 1,
    "Microcephaly_1|_primary|_autosomal_recessive|not_provided|Autosomal_recessive_primary_microcephaly": 1,
    "Keloid_formation": 1,
    "MFHAS1-related_disorder": 12,
    "not_provided|MFHAS1-related_disorder": 1,
    "MFHAS1-related_disorder|not_provided": 1,
    "ERI1-related_disorder": 10,
    "Spondyloepimetaphyseal_dysplasia|_Guo-Campeau_type": 5,
    "ERI1-related_disorder|not_provided": 3,
    "ERI1-related_disorder|not_specified": 1,
    "Hoxha-Aliu_syndrome": 3,
    "Spondyloepimetaphyseal_dysplasia|_Guo-Campeau_type|See_cases": 2,
    "Abnormal_finger_morphology|Coarse_facial_features|Unilateral_renal_agenesis|Global_developmental_delay": 1,
    "Hoxha-Aliu_syndrome|ERI1-associated_disorder": 1,
    "MSRA-related_disorder": 5,
    "Occult_macular_dystrophy": 148,
    "not_provided|Occult_macular_dystrophy": 40,
    "Occult_macular_dystrophy|not_provided": 51,
    "Occult_macular_dystrophy|Inborn_genetic_diseases": 13,
    "not_specified|Occult_macular_dystrophy|RP1L1-related_disorder|not_provided": 1,
    "Occult_macular_dystrophy|Retinal_dystrophy|not_provided": 5,
    "Occult_macular_dystrophy|not_provided|not_specified": 2,
    "RP1L1-related_disorder": 22,
    "not_specified|Occult_macular_dystrophy|Retinitis_pigmentosa_88|Retinal_dystrophy|not_provided": 2,
    "not_specified|Occult_macular_dystrophy|not_provided": 6,
    "Inborn_genetic_diseases|Occult_macular_dystrophy": 17,
    "Occult_macular_dystrophy|Retinal_dystrophy": 9,
    "Inborn_genetic_diseases|Occult_macular_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Occult_macular_dystrophy": 11,
    "Retinitis_pigmentosa_88": 14,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_specified|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_88|Occult_macular_dystrophy|not_provided": 3,
    "Retinitis_pigmentosa_88|Occult_macular_dystrophy|Retinal_dystrophy|not_provided": 1,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|Retinal_dystrophy|not_provided": 3,
    "not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88|Retinal_dystrophy": 3,
    "Retinal_dystrophy|Occult_macular_dystrophy|not_provided": 4,
    "Occult_macular_dystrophy|not_provided|Retinitis_pigmentosa_88|Retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_88|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88|Retinal_dystrophy": 2,
    "not_specified|not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_88|Occult_macular_dystrophy": 1,
    "Occult_macular_dystrophy|Inborn_genetic_diseases|not_provided": 4,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|Inborn_genetic_diseases": 1,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_provided": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_88|Occult_macular_dystrophy": 1,
    "not_provided|Occult_macular_dystrophy|RP1L1-related_disorder": 2,
    "Occult_macular_dystrophy|not_specified|not_provided": 10,
    "Inborn_genetic_diseases|Occult_macular_dystrophy|Retinitis_pigmentosa_88": 4,
    "Inborn_genetic_diseases|not_provided|Occult_macular_dystrophy": 3,
    "Retinal_dystrophy|RP1L1-related_disorder": 3,
    "not_specified|not_provided|Occult_macular_dystrophy|Retinal_dystrophy": 1,
    "not_provided|RP1L1-related_disorder": 3,
    "Occult_macular_dystrophy|not_provided|RP1L1-related_disorder": 2,
    "Occult_macular_dystrophy|RP1L1-related_disorder": 4,
    "not_specified|Occult_macular_dystrophy": 2,
    "Retinal_dystrophy|Occult_macular_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "RP1L1-related_disorder|Retinal_dystrophy": 2,
    "Occult_macular_dystrophy|not_provided|Retinal_dystrophy": 5,
    "Occult_macular_dystrophy|Inborn_genetic_diseases|not_provided|RP1L1-related_disorder": 1,
    "not_specified|Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_provided": 3,
    "Inborn_genetic_diseases|RP1L1-related_disorder": 5,
    "not_provided|Occult_macular_dystrophy|Retinal_dystrophy": 3,
    "Retinitis_pigmentosa_88|Occult_macular_dystrophy": 2,
    "not_specified|not_provided|Occult_macular_dystrophy": 2,
    "not_provided|Retinitis_pigmentosa_88|Occult_macular_dystrophy": 2,
    "not_provided|Occult_macular_dystrophy|not_specified": 5,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88": 7,
    "Retinitis_pigmentosa_88|Occult_macular_dystrophy|not_specified|not_provided": 1,
    "not_provided|not_specified|Occult_macular_dystrophy": 5,
    "Retinitis_pigmentosa_88|not_specified|Occult_macular_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_88|Autosomal_recessive_retinitis_pigmentosa": 1,
    "RP1L1-related_disorder|not_provided": 3,
    "Occult_macular_dystrophy|RP1L1-related_disorder|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Occult_macular_dystrophy|See_cases": 1,
    "not_provided|Occult_macular_dystrophy|Retinal_dystrophy|not_specified": 1,
    "not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88|Retinal_dystrophy|not_specified": 1,
    "Retinal_dystrophy|Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_provided": 1,
    "RP1L1-related_disorder|Inborn_genetic_diseases": 3,
    "RP1L1-related_disorder|Occult_macular_dystrophy": 6,
    "not_provided|Inborn_genetic_diseases|Occult_macular_dystrophy": 2,
    "not_specified|Retinal_dystrophy|Occult_macular_dystrophy": 1,
    "not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88|RP1L1-related_disorder": 1,
    "Retinal_dystrophy|Occult_macular_dystrophy|not_provided|Retinitis_pigmentosa_88": 1,
    "Inborn_genetic_diseases|RP1L1-related_disorder|Occult_macular_dystrophy": 2,
    "not_provided|Retinitis_pigmentosa_88|Retinal_dystrophy": 1,
    "Stargardt_disease|Inborn_genetic_diseases|Retinal_dystrophy|RP1L1-related_disorder": 1,
    "Occult_macular_dystrophy|not_provided|Inborn_genetic_diseases|RP1L1-related_disorder": 1,
    "Occult_macular_dystrophy|RP1L1-related_disorder|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_provided|Occult_macular_dystrophy": 2,
    "Occult_macular_dystrophy|Inborn_genetic_diseases|RP1L1-related_disorder": 2,
    "RP1L1-related_disorder|Occult_macular_dystrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_88|Occult_macular_dystrophy|not_provided|Retinal_dystrophy": 1,
    "not_provided|Occult_macular_dystrophy|RP1L1-related_disorder|Retinal_dystrophy": 2,
    "not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_specified|Retinal_dystrophy": 3,
    "not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88": 4,
    "Retinal_dystrophy|Retinitis_pigmentosa_88": 1,
    "Occult_macular_dystrophy|not_provided|Inborn_genetic_diseases": 4,
    "RP1L1-related_disorder|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|RP1L1-related_disorder": 1,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_88|RP1L1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Occult_macular_dystrophy|not_provided|RP1L1-related_disorder": 2,
    "not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_specified": 1,
    "RP1L1-related_disorder|Occult_macular_dystrophy|not_provided": 2,
    "RP1L1-related_disorder|Optic_atrophy|not_provided": 1,
    "not_provided|Retinal_dystrophy|Occult_macular_dystrophy": 2,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_specified|not_provided|Retinal_dystrophy": 1,
    "not_provided|RP1L1-related_disorder|Occult_macular_dystrophy": 1,
    "not_provided|Retinal_dystrophy|RP1L1-related_disorder|Occult_macular_dystrophy": 2,
    "Retinitis_pigmentosa_88|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_88|Occult_macular_dystrophy|Retinal_dystrophy": 1,
    "RP1L1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Occult_macular_dystrophy|Retinitis_pigmentosa_88": 1,
    "Occult_macular_dystrophy|Retinitis_pigmentosa_88|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_specified|Occult_macular_dystrophy|not_provided": 1,
    "Occult_macular_dystrophy|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_88|Retinal_dystrophy|not_provided": 2,
    "Ulnar/fibula_ray_defect-brachydactyly_syndrome|not_provided|Occult_macular_dystrophy": 1,
    "RP1L1-related_disorder|Retinitis_pigmentosa_88|Occult_macular_dystrophy|not_provided": 1,
    "Occult_macular_dystrophy|not_provided|RP1L1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Retinal_dystrophy|not_specified|Occult_macular_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_88|Occult_macular_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Occult_macular_dystrophy|Retinal_dystrophy|not_specified|RP1L1-related_disorder": 1,
    "Retinitis_pigmentosa_88|Optic_atrophy|Retinal_dystrophy|not_provided|Occult_macular_dystrophy": 1,
    "Occult_macular_dystrophy|Inborn_genetic_diseases|not_provided|Retinal_dystrophy": 1,
    "SOX7-related_disorder": 3,
    "SOX7-related_disorder|not_provided": 1,
    "BLK-related_disorder": 15,
    "Maturity-onset_diabetes_of_the_young_type_11": 53,
    "Maturity-onset_diabetes_of_the_young_type_11|not_provided": 15,
    "Maturity-onset_diabetes_of_the_young_type_11|not_provided|Systemic_lupus_erythematosus": 5,
    "not_provided|Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_11": 9,
    "BLK-related_disorder|not_provided": 4,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus": 2,
    "not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "not_specified|Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11|not_provided": 2,
    "not_provided|Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus": 1,
    "Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11|Monogenic_diabetes|not_provided": 1,
    "Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11|not_provided": 1,
    "Monogenic_diabetes|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_11|not_specified": 1,
    "Systemic_lupus_erythematosus|not_provided": 3,
    "not_provided|not_specified|Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "not_provided|BLK-related_disorder": 1,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_11": 3,
    "Systemic_lupus_erythematosus|not_provided|Maturity-onset_diabetes_of_the_young_type_11|not_specified": 1,
    "BLK-related_disorder|Systemic_lupus_erythematosus|not_provided": 1,
    "not_specified|not_provided|Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus|not_specified": 1,
    "BLK-related_disorder|not_provided|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "not_specified|BLK-related_disorder|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|not_provided|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|Monogenic_diabetes": 1,
    "BLK-related_disorder|not_provided|Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus": 1,
    "Monogenic_diabetes|not_specified|not_provided|Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "BLK-related_disorder|not_specified": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_11|not_provided": 2,
    "Maturity-onset_diabetes_of_the_young_type_11|not_specified": 2,
    "Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus|not_specified|not_provided": 1,
    "BLK-related_disorder|Maturity-onset_diabetes_of_the_young_type_11|not_specified|not_provided": 1,
    "Systemic_lupus_erythematosus|Maturity-onset_diabetes_of_the_young_type_11|Monogenic_diabetes": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|not_specified|not_provided|Systemic_lupus_erythematosus": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus|not_specified|Monogenic_diabetes|not_provided|BLK-related_disorder": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|not_provided|BLK-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|Systemic_lupus_erythematosus|not_provided": 3,
    "not_provided|BLK-related_disorder|Maturity-onset_diabetes_of_the_young_type_11": 1,
    "Maturity-onset_diabetes_of_the_young_type_11|BLK-related_disorder|not_specified": 1,
    "Atrioventricular_septal_defect_4": 398,
    "GATA4-related_disorder": 18,
    "GATA4-related_disorder|not_provided": 1,
    "not_provided|Atrioventricular_septal_defect_4": 32,
    "Atrioventricular_septal_defect_4|not_provided": 28,
    "Atrioventricular_septal_defect_4|Cardiovascular_phenotype": 64,
    "Cardiovascular_phenotype|Atrioventricular_septal_defect_4": 49,
    "Atrioventricular_septal_defect_4|Cardiovascular_phenotype|not_provided": 5,
    "not_provided|Cardiovascular_phenotype|Atrioventricular_septal_defect_4": 7,
    "Cardiovascular_phenotype|Atrioventricular_septal_defect_4|not_provided": 4,
    "Testicular_anomalies_with_or_without_congenital_heart_disease|not_provided|Atrioventricular_septal_defect_4|Intellectual_disability": 1,
    "Cardiovascular_phenotype|not_provided|Atrioventricular_septal_defect_4": 6,
    "Atrial_septal_defect_2|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4": 1,
    "Atrioventricular_septal_defect_4|not_provided|Cardiovascular_phenotype": 8,
    "Atrioventricular_septal_defect_4|GATA4-related_disorder|Cardiovascular_phenotype": 2,
    "Atrioventricular_septal_defect_4|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "GATA4-related_disorder|Atrioventricular_septal_defect_4": 1,
    "Cardiovascular_phenotype|Ventricular_septal_defect_1": 1,
    "Atrioventricular_septal_defect_4|Intellectual_disability": 1,
    "not_provided|Atrioventricular_septal_defect_4|Cardiovascular_phenotype": 7,
    "Atrial_septal_defect_2": 8,
    "Atrioventricular_septal_defect_4|not_provided|Cardiovascular_phenotype|Testicular_anomalies_with_or_without_congenital_heart_disease|Atrial_septal_defect_2|Tetralogy_of_Fallot|Ventricular_septal_defect_1": 1,
    "Atrioventricular_septal_defect_4|Ventricular_septal_defect_1|Atrial_septal_defect_2|Tetralogy_of_Fallot|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "Cardiovascular_phenotype|GATA4-related_disorder|not_specified|not_provided|Atrioventricular_septal_defect_4": 1,
    "Tetralogy_of_Fallot|not_provided|Testicular_anomalies_with_or_without_congenital_heart_disease|Cardiovascular_phenotype|Atrioventricular_septal_defect_4": 1,
    "Atrioventricular_septal_defect_4|not_provided|Atrial_septal_defect_2|Ventricular_septal_defect_1|Tetralogy_of_Fallot|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "not_provided|Cardiovascular_phenotype|Atrioventricular_septal_defect_4|not_specified": 1,
    "Cardiovascular_phenotype|GATA4-related_disorder": 1,
    "not_provided|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "Testicular_anomalies_with_or_without_congenital_heart_disease": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Atrioventricular_septal_defect_4": 1,
    "GATA4-related_disorder|Atrioventricular_septal_defect_4|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Tetralogy_of_Fallot|Atrial_septal_defect_2|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "Atrioventricular_septal_defect_4|not_specified": 1,
    "Atrioventricular_septal_defect_4|not_provided|GATA4-related_disorder": 1,
    "not_provided|not_specified|Atrioventricular_septal_defect_4|Cardiovascular_phenotype": 1,
    "not_specified|Atrioventricular_septal_defect_4|Cardiovascular_phenotype": 1,
    "Congenital_heart_disease|Structural_congenital_heart_disease|_multiple_types_-_GATA4|not_specified|not_provided": 1,
    "Congenital_heart_disease|not_specified|not_provided": 1,
    "not_specified|Atrioventricular_septal_defect_4|not_provided": 1,
    "Atrioventricular_septal_defect_4|Renal_cysts_and_diabetes_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_septal_defect_2|Ventricular_septal_defect_1|Tetralogy_of_Fallot|Atrioventricular_septal_defect_4|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "46|XY_sex_reversal_3": 37,
    "Atrial_septal_defect_2|Ventricular_septal_defect_1|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Atrioventricular_septal_defect_4": 1,
    "not_provided|Atrioventricular_septal_defect_4|not_specified|GATA4-related_disorder|Cardiovascular_phenotype": 1,
    "Atrioventricular_septal_defect_4|GATA4-related_disorder": 5,
    "GATA4-related_disorder|Cardiovascular_phenotype|Atrioventricular_septal_defect_4|not_provided": 1,
    "Tetralogy_of_Fallot|Testicular_anomalies_with_or_without_congenital_heart_disease|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Atrial_septal_defect_2": 1,
    "Atrial_septal_defect_2|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Primary_dilated_cardiomyopathy|Atrial_septal_defect_2|Tetralogy_of_Fallot": 1,
    "Atrioventricular_septal_defect_4|Atrial_septal_defect_2|Cardiovascular_phenotype|not_provided": 1,
    "Atrioventricular_septal_defect_4|Atrial_septal_defect_2": 3,
    "Atrial_septal_defect_2|GATA4-related_disorder|Atrioventricular_septal_defect_4|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "Atrioventricular_septal_defect_4|Cardiovascular_phenotype|not_specified": 1,
    "Transposition_of_the_great_arteries|Atrioventricular_septal_defect_4|Atrial_septal_defect_2": 1,
    "Cardiovascular_phenotype|Atrioventricular_septal_defect_4|not_provided|GATA4-related_disorder": 1,
    "Atrioventricular_septal_defect_4|Testicular_anomalies_with_or_without_congenital_heart_disease": 1,
    "Congenital_heart_disease|not_specified|Testicular_anomalies_with_or_without_congenital_heart_disease|Structural_congenital_heart_disease|_multiple_types_-_GATA4|GATA4-related_disorder|not_provided": 1,
    "GATA4-related_disorder|Atrial_septal_defect_2": 1,
    "GATA4-related_disorder|Ventricular_septal_defect_1|not_provided|Atrioventricular_septal_defect_4": 1,
    "not_provided|Atrioventricular_septal_defect_4|GATA4-related_disorder": 1,
    "not_provided|Atrioventricular_septal_defect_4|GATA4-related_disorder|Testicular_anomalies_with_or_without_congenital_heart_disease|Atrial_septal_defect_2|Tetralogy_of_Fallot|Ventricular_septal_defect_1": 1,
    "Atrioventricular_septal_defect_4|Atrial_septal_defect_2|not_provided": 1,
    "Testicular_anomalies_with_or_without_congenital_heart_disease|Atrioventricular_septal_defect_4": 1,
    "not_specified|not_provided|Congenital_heart_disease|Atrioventricular_septal_defect_4|GATA4-related_disorder": 1,
    "not_specified|Congenital_heart_disease|GATA4-related_disorder": 1,
    "Atrioventricular_septal_defect_4|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Atrioventricular_septal_defect_4|not_provided|Intellectual_disability": 1,
    "GATA4-related_disorder|46|XY_sex_reversal_3|not_provided|not_specified|Cardiovascular_phenotype|Atrioventricular_septal_defect_4": 1,
    "Atrioventricular_septal_defect_4|not_specified|not_provided": 1,
    "Atrioventricular_septal_defect_4|not_provided|Tetralogy_of_Fallot|Testicular_anomalies_with_or_without_congenital_heart_disease|Ventricular_septal_defect_1|Atrial_septal_defect_2": 1,
    "Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "Inborn_genetic_diseases|Atrioventricular_septal_defect_4|not_provided": 1,
    "Atrioventricular_septal_defect_4|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "not_specified|Atrioventricular_septal_defect_4|GATA4-related_disorder": 1,
    "not_specified|Atrioventricular_septal_defect_4|Cardiovascular_phenotype|Neonatal_insulin-dependent_diabetes_mellitus|not_provided": 1,
    "Atrioventricular_septal_defect_4|Cardiovascular_phenotype|GATA4-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Atrioventricular_septal_defect_4|Neonatal_insulin-dependent_diabetes_mellitus|GATA4-related_disorder|not_provided": 1,
    "Testicular_anomalies_with_or_without_congenital_heart_disease|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Atrial_septal_defect_2|Tetralogy_of_Fallot|not_provided": 1,
    "not_specified|Congenital_heart_disease|not_provided": 2,
    "not_specified|Congenital_heart_disease|not_provided|Structural_congenital_heart_disease|_multiple_types_-_GATA4": 1,
    "not_provided|Atrioventricular_septal_defect_4|not_specified": 1,
    "not_provided|46|XY_sex_reversal_3|Atrioventricular_septal_defect_4|not_specified": 1,
    "GATA4-related_disorder|Atrioventricular_septal_defect_4|not_provided": 1,
    "Testicular_anomalies_with_or_without_congenital_heart_disease|not_provided|not_specified|Atrioventricular_septal_defect_4|Ventricular_septal_defect_1|Atrial_septal_defect_2|46|XY_sex_reversal_3|Tetralogy_of_Fallot|Microcephaly": 1,
    "Tetralogy_of_Fallot|Cardiovascular_phenotype|Atrioventricular_septal_defect_4": 1,
    "Atrioventricular_septal_defect_4|Testicular_anomalies_with_or_without_congenital_heart_disease|not_specified|GATA4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "GATA4-related_disorder|Atrial_septal_defect_2|Testicular_anomalies_with_or_without_congenital_heart_disease|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Tetralogy_of_Fallot|Cardiovascular_phenotype|Thoracic_aortic_aneurysm|not_provided|not_specified": 1,
    "Tetralogy_of_Fallot|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Testicular_anomalies_with_or_without_congenital_heart_disease|Atrial_septal_defect_2|not_provided": 1,
    "Brugada_syndrome|Atrioventricular_septal_defect_4": 1,
    "Atrioventricular_septal_defect_4|Tetralogy_of_Fallot|Congenital_heart_disease|Ventricular_septal_defect_1|Testicular_anomalies_with_or_without_congenital_heart_disease|Atrial_septal_defect_2|not_provided|GATA4-related_disorder|not_specified|Pulmonic_stenosis|Tricuspid_regurgitation|Pulmonary_valve_atresia|Inborn_genetic_diseases": 1,
    "Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Atrial_septal_defect_2|Testicular_anomalies_with_or_without_congenital_heart_disease|Tetralogy_of_Fallot|not_provided": 1,
    "Atrial_septal_defect_2|Tetralogy_of_Fallot|Ventricular_septal_defect_1|Atrioventricular_septal_defect_4|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Atrioventricular_septal_defect_4|Ventricular_septal_defect_1": 1,
    "not_provided|GATA4-related_disorder": 1,
    "not_provided|Achondroplasia|Structural_congenital_heart_disease|_multiple_types_-_GATA4|GATA4-related_disorder|Congenital_heart_disease": 1,
    "Congenital_heart_disease|not_specified|GATA4-related_disorder": 1,
    "not_provided|Achondroplasia|not_specified|Congenital_heart_disease": 1,
    "Squalene_synthase_deficiency": 6,
    "FDFT1-related_disorder": 17,
    "not_provided|FDFT1-related_disorder": 4,
    "FDFT1-related_disorder|not_provided": 6,
    "not_specified|FDFT1-related_disorder": 3,
    "FDFT1-related_disorder|not_specified|not_provided": 1,
    "Squalene_synthase_deficiency|not_provided": 3,
    "Squalene_synthase_deficiency|FDFT1-related_disorder|not_provided": 2,
    "FDFT1-related_disorder|Squalene_synthase_deficiency": 1,
    "not_provided|Squalene_synthase_deficiency": 1,
    "CTSB-related_disorder|not_provided": 2,
    "not_provided|CTSB-related_disorder": 7,
    "Keratolytic_winter_erythema|not_provided": 1,
    "CTSB-related_disorder": 2,
    "Keratolytic_winter_erythema|CTSB-related_disorder|not_provided": 1,
    "not_provided|Keratolytic_winter_erythema": 1,
    "DLC1-related_disorder": 16,
    "not_provided|not_specified|Colorectal_cancer": 4,
    "DLC1-related_disorder|not_provided": 12,
    "DLC1-related_disorder|Colorectal_cancer|not_provided": 3,
    "not_specified|Colorectal_cancer": 12,
    "not_specified|Colorectal_cancer|not_provided": 2,
    "not_provided|Colorectal_cancer": 14,
    "DLC1-related_disorder|not_specified": 1,
    "not_provided|DLC1-related_disorder": 13,
    "not_provided|DLC1-related_disorder|Colorectal_cancer": 2,
    "not_specified|not_provided|DLC1-related_disorder": 2,
    "Colorectal_cancer|not_specified|not_provided": 5,
    "Colorectal_cancer|DLC1-related_disorder": 2,
    "DLC1-related_disorder|not_specified|not_provided|Colorectal_cancer": 1,
    "Colorectal_cancer|not_specified": 5,
    "not_specified|not_provided|Colorectal_cancer": 3,
    "not_provided|Colorectal_cancer|not_specified": 2,
    "DLC1-related_disorder|not_specified|not_provided": 2,
    "Colorectal_cancer|DLC1-related_disorder|not_provided|not_specified": 1,
    "Colorectal_cancer|not_provided|not_specified": 2,
    "DLC1-related_disorder|not_provided|Colorectal_cancer": 1,
    "not_specified|DLC1-related_disorder|Colorectal_cancer|not_provided": 1,
    "DLC1-related_disorder|Colorectal_cancer": 1,
    "Colorectal_cancer|not_provided|DLC1-related_disorder": 1,
    "TUSC3-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_7": 53,
    "Congenital_disorder_of_glycosylation|not_specified": 5,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|Intellectual_disability|_autosomal_recessive_7": 1,
    "Intellectual_disability|_autosomal_recessive_7|not_provided|Congenital_disorder_of_glycosylation|TUSC3-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_7": 1,
    "Intellectual_disability|_autosomal_recessive_7|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_7|Abnormality_of_the_nervous_system": 1,
    "TUSC3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Congenital_disorder_of_glycosylation|Intellectual_disability|_autosomal_recessive_7": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_7": 2,
    "not_specified|not_provided|Congenital_disorder_of_glycosylation|Intellectual_disability|_autosomal_recessive_7": 1,
    "Congenital_disorder_of_glycosylation|Intellectual_disability|_autosomal_recessive_7": 2,
    "Congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 2,
    "not_specified|Congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_7": 1,
    "Intellectual_disability|_autosomal_recessive_7|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_24|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_7|Intellectual_disability": 1,
    "TUSC3-related_disorder|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_7|not_specified": 1,
    "MSR1-related_disorder": 7,
    "MSR1-related_disorder|not_provided": 4,
    "Barrett_esophagus": 3,
    "Barrett_esophagus|Prostate_cancer|not_provided|X-linked_Alport_syndrome|MSR1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "BARRETT_ESOPHAGUS/ESOPHAGEAL_ADENOCARCINOMA": 2,
    "Preeclampsia|Normal_pregnancy": 2,
    "FGF20-related_disorder": 9,
    "Renal_hypodysplasia/aplasia_2": 2,
    "not_provided|FGF20-related_disorder": 2,
    "FGF20-related_disorder|not_provided": 1,
    "Renal_hypodysplasia/aplasia_2|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_53|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_53": 99,
    "Hereditary_spastic_paraplegia_53|VPS37A-related_disorder": 3,
    "Hereditary_spastic_paraplegia_53|not_provided": 5,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_53": 1,
    "Hereditary_spastic_paraplegia_53|not_specified": 9,
    "VPS37A-related_disorder": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_53": 1,
    "VPS37A-related_disorder|Hereditary_spastic_paraplegia_53": 2,
    "not_specified|Hereditary_spastic_paraplegia_53": 10,
    "not_specified|Hereditary_spastic_paraplegia_53|not_provided": 2,
    "Hereditary_spastic_paraplegia_53|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_53|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_53|not_provided": 1,
    "Idiopathic_transverse_myelitis|Hereditary_spastic_paraplegia_53|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_53|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_53|Hereditary_spastic_paraplegia|not_provided": 1,
    "MTMR7-related_disorder": 6,
    "SLC7A2-related_disorder": 11,
    "Normal_pregnancy|Large_for_gestational_age": 3,
    "Normal_pregnancy|Small_for_gestational_age|Preeclampsia": 1,
    "PCM1-related_disorder": 8,
    "Thyroid_cancer|_nonmedullary|_1": 4,
    "PCM1-related_disorder|not_provided": 1,
    "not_provided|PCM1-related_disorder": 1,
    "Farber_lipogranulomatosis|not_provided": 28,
    "Farber_lipogranulomatosis": 69,
    "not_provided|Farber_lipogranulomatosis": 30,
    "Farber_lipogranulomatosis|not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 3,
    "Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 3,
    "Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_provided": 6,
    "ASAH1-related_sphingolipidosis": 1,
    "Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 6,
    "Variant_of_unknown_significance|not_provided|Keloid_formation": 1,
    "Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis|not_provided": 9,
    "ASAH1-related_disorders|not_specified|not_provided|Farber_lipogranulomatosis": 1,
    "not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis": 3,
    "ASAH1-related_disorders|not_provided|Farber_lipogranulomatosis": 2,
    "Abnormality_of_metabolism/homeostasis|Farber_lipogranulomatosis|not_provided": 1,
    "ASAH1-related_disorders|not_provided": 4,
    "not_provided|ASAH1-related_disorders": 5,
    "not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 2,
    "not_specified|not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis": 1,
    "Farber_lipogranulomatosis|not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_specified": 3,
    "ASAH1-related_disorders|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|not_specified|not_provided|Farber_lipogranulomatosis": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Inborn_genetic_diseases|Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 1,
    "Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis": 2,
    "Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_provided": 3,
    "not_provided|Farber_lipogranulomatosis|Inborn_genetic_diseases": 1,
    "not_provided|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 3,
    "not_provided|Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_specified": 1,
    "Farber_lipogranulomatosis|Inborn_genetic_diseases|not_provided": 1,
    "ASAH1-related_disorders|not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 2,
    "ASAH1-related_disorders|Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_provided": 1,
    "Farber_lipogranulomatosis|not_specified|not_provided": 1,
    "Farber_lipogranulomatosis|not_provided|not_specified": 1,
    "not_provided|Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 3,
    "not_provided|not_specified|Farber_lipogranulomatosis": 1,
    "not_specified|Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_provided": 1,
    "not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis|not_specified": 1,
    "not_provided|ASAH1-related_disorders|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis": 1,
    "Farber_lipogranulomatosis|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_specified|not_provided": 1,
    "Farber_lipogranulomatosis|not_specified|not_provided|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome": 1,
    "ASAH1-related_disorders": 3,
    "Farber_lipogranulomatosis|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "not_specified|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|Farber_lipogranulomatosis|not_provided": 1,
    "Farber_lipogranulomatosis|not_specified|Spinal_muscular_atrophy-progressive_myoclonic_epilepsy_syndrome|not_provided": 1,
    "ASAH1-related_disorders|Farber_lipogranulomatosis": 1,
    "ASAH1-related_sphingolipidosis|Self-limited_epilepsy_with_centrotemporal_spikes|not_specified|not_provided": 1,
    "not_specified|not_provided|NAT1*17_ALLELE": 1,
    "Slow_acetylator_due_to_N-acetyltransferase_enzyme_variant|NAT2-related_disorder": 1,
    "NAT2-related_disorder": 6,
    "NAT2-related_disorder|Slow_acetylator_due_to_N-acetyltransferase_enzyme_variant": 2,
    "Slow_acetylator_due_to_N-acetyltransferase_enzyme_variant": 2,
    "PSD3-related_disorder": 3,
    "PSD3-related_disorder|not_provided": 2,
    "CSGALNACT1-related_disorder": 5,
    "not_provided|CSGALNACT1-related_disorder": 6,
    "CSGALNACT1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age|not_provided|CSGALNACT1-related_disorder": 1,
    "not_provided|CSGALNACT1-related_disorder|Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age": 2,
    "Inborn_genetic_diseases|Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age": 1,
    "Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age": 6,
    "not_provided|Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age": 5,
    "Inborn_genetic_diseases|CSGALNACT1-related_disorder": 1,
    "Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age|CSGALNACT1-related_disorder|not_provided": 1,
    "Skeletal_dysplasia|_mild|_with_joint_laxity_and_advanced_bone_age|not_provided": 1,
    "CSGALNACT1-related_disorder|Inborn_genetic_diseases": 1,
    "Hyperlipoproteinemia|_type_I": 118,
    "not_provided|Hyperlipoproteinemia|_type_I": 25,
    "not_provided|Hyperlipidemia|_familial_combined|_susceptibility_to|Hyperlipoproteinemia|_type_I": 1,
    "not_provided|not_specified|LPL-related_disorder": 2,
    "Hyperlipidemia|_familial_combined|_susceptibility_to|not_specified": 1,
    "Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related": 9,
    "Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_specified": 1,
    "LPL-related_disorder|Hyperlipoproteinemia|_type_I|not_provided": 1,
    "Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I|not_provided": 1,
    "Hyperlipoproteinemia|_type_I|not_provided|Cardiovascular_phenotype": 2,
    "Hyperlipidemia|_familial_combined|_LPL_related": 10,
    "not_specified|Hyperlipoproteinemia|_type_I": 2,
    "Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|Coronary_heart_disease|not_provided|Hyperlipidemia|_familial_combined|_susceptibility_to|Cardiovascular_phenotype|LPL-related_disorder|not_specified": 1,
    "not_provided|LPL-related_disorder|not_specified|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1A|not_specified|not_provided|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hyperlipoproteinemia|_type_I": 1,
    "not_provided|not_specified|Hyperlipoproteinemia|_type_I|LPL-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Hyperlipoproteinemia|_type_I|not_specified": 2,
    "LPL-related_disorder|Hyperlipoproteinemia|_type_I|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Hyperlipoproteinemia|_type_I|not_provided": 14,
    "Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype": 1,
    "Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I": 4,
    "Hyperlipoproteinemia|_type_I|not_provided|Hyperlipidemia|_familial_combined|_LPL_related|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_provided": 3,
    "Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_provided": 3,
    "LPL-related_disorder": 2,
    "not_provided|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype": 2,
    "not_provided|Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|LPL-related_disorder|Cardiovascular_phenotype": 1,
    "Hyperlipoproteinemia|_type_I|not_specified": 1,
    "Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_provided": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Hyperlipoproteinemia|_type_I": 1,
    "not_provided|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related": 2,
    "Hyperlipidemia|_familial_combined|_LPL_related|not_provided": 2,
    "not_specified|Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I": 3,
    "Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related": 3,
    "not_specified|Hyperlipoproteinemia|_type_I|not_provided|Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "Hyperlipoproteinemia|_type_I|not_specified|not_provided": 1,
    "not_specified|Hyperlipoproteinemia|_type_I|not_provided|Cardiovascular_phenotype": 3,
    "Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|Cardiovascular_phenotype": 1,
    "not_provided|LPL-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|LPL-related_disorder|Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related": 1,
    "not_provided|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_specified": 1,
    "LPL-related_disorder|not_provided|Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I|not_specified": 1,
    "Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_provided|Cardiovascular_phenotype|LPL-related_disorder": 1,
    ".|Hyperlipoproteinemia|_type_I": 1,
    "Hyperlipoproteinemia|_type_I|not_provided|Hyperlipidemia|_familial_combined|_LPL_related": 1,
    "Hypertriglyceridemia|Hyperlipoproteinemia|_type_I|not_provided": 1,
    "not_provided|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_specified|LPL-related_disorder": 1,
    "Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_specified|not_provided|LPL-related_disorder": 1,
    "Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|not_provided|Cardiovascular_phenotype": 1,
    "Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hyperlipoproteinemia|_type_I": 4,
    "not_provided|Hyperlipidemia|_familial_combined|_LPL_related": 1,
    "not_provided|Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I": 1,
    "Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Hyperlipidemia|_familial_combined|_LPL_related": 1,
    "Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|Hyperlipidemia|_familial_combined|_susceptibility_to|not_provided|not_specified": 1,
    "Hyperlipoproteinemia|_type_I|LIPOPROTEIN_LIPASE_(OLBIA)": 1,
    "Hyperlipoproteinemia|_type_I|not_provided|Lipase_deficiency|_combined": 1,
    "Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Hyperlipoproteinemia|_type_I|LPL-related_disorder|Hyperlipidemia|_familial_combined|_LPL_related": 1,
    "not_provided|Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I": 1,
    "Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I": 2,
    "Hyperlipoproteinemia|_type_I|LPL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hyperlipoproteinemia|_type_I|Cardiovascular_phenotype|not_specified|LPL-related_disorder|not_provided": 1,
    "Hyperlipoproteinemia|_type_I|not_provided|Cardiovascular_phenotype|LPL-related_disorder": 1,
    "not_specified|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|LPL-related_disorder": 1,
    "not_provided|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_11": 1,
    "not_specified|Cardiovascular_phenotype|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_provided|LPL-related_disorder": 1,
    "Hyperlipidemia|_familial_combined|_LPL_related|Hyperlipoproteinemia|_type_I|not_provided": 1,
    "not_specified|Hyperlipoproteinemia|_type_I|Hyperlipidemia|_familial_combined|_LPL_related|not_provided|Cardiovascular_phenotype|LPL-related_disorder": 1,
    "not_specified|Hyperlipoproteinemia|_type_I|not_provided|Dystrophin_deficiency": 1,
    "Hyperlipoproteinemia|_type_I|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_11|not_provided": 1,
    "ATP6V1B2-related_disorder": 6,
    "Autosomal_dominant_deafness_-_onychodystrophy_syndrome|Zimmermann-Laband_syndrome_2|Inborn_genetic_diseases|Cataract_10_multiple_types": 1,
    "Zimmermann-Laband_syndrome_2": 10,
    "not_provided|Autosomal_dominant_deafness_-_onychodystrophy_syndrome|Zimmermann-Laband_syndrome_2": 1,
    "Autosomal_dominant_deafness_-_onychodystrophy_syndrome": 3,
    "Zimmermann-Laband_syndrome_2|Autosomal_dominant_deafness_-_onychodystrophy_syndrome": 1,
    "Autosomal_dominant_deafness_-_onychodystrophy_syndrome|Zimmermann-Laband_syndrome_2": 1,
    "Zimmermann-Laband_syndrome_2|ATP6V1B2_related_neurodevelopmental_disorders": 1,
    "not_provided|ATP6V1B2-related_disorder": 1,
    "Autosomal_dominant_deafness_-_onychodystrophy_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_deafness_-_onychodystrophy_syndrome": 1,
    "Zimmermann-Laband_syndrome_1|Zimmermann-Laband_syndrome_2": 1,
    "Zimmermann-Laband_syndrome_with_epileptic_encephalopathy": 1,
    "Autosomal_dominant_deafness_-_onychodystrophy_syndrome|not_provided": 1,
    "Autosomal_dominant_deafness_-_onychodystrophy_syndrome|Zimmermann-Laband_syndrome_2|not_provided|Neurodevelopmental_delay": 1,
    "not_provided|Autosomal_dominant_deafness_-_onychodystrophy_syndrome": 1,
    "LZTS1-related_disorder": 4,
    "not_provided|not_specified|LZTS1-related_disorder": 1,
    "not_provided|LZTS1-related_disorder": 9,
    "LZTS1-related_disorder|not_provided": 8,
    "Esophageal_squamous_cell_carcinoma|_somatic": 5,
    "Pazopanib_response": 1,
    "not_provided|FGF17-related_disorder": 1,
    "FGF17-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_20_with_or_without_anosmia": 2,
    "Hypogonadotropic_hypogonadism_20_without_anosmia": 1,
    "not_provided|Hypogonadotropic_hypogonadism_20_with_or_without_anosmia": 1,
    "Atrichia_with_papular_lesions|Alopecia_universalis_congenita": 59,
    "Alopecia_universalis_congenita|Atrichia_with_papular_lesions": 21,
    "Alopecia_universalis|Atrichia_with_papular_lesions": 1,
    "not_provided|Atrichia_with_papular_lesions|Alopecia_universalis_congenita": 29,
    "Atrichia_with_papular_lesions|not_provided|Alopecia_universalis_congenita": 7,
    "Atrichia_with_papular_lesions": 9,
    "Alopecia_universalis_congenita|not_provided|Atrichia_with_papular_lesions": 2,
    "not_provided|Atrichia_with_papular_lesions|Intellectual_disability|_autosomal_dominant_14|Alopecia_universalis_congenita": 1,
    "Alopecia_universalis_congenita": 10,
    "Alopecia_universalis_congenita|Inborn_genetic_diseases|Atrichia_with_papular_lesions": 2,
    "HR-related_disorder|not_provided|Alopecia_universalis_congenita|Atrichia_with_papular_lesions": 2,
    "Atrichia_with_papular_lesions|Alopecia_universalis_congenita|not_provided": 7,
    "not_provided|Alopecia_universalis_congenita|Atrichia_with_papular_lesions": 10,
    "not_provided|Atrichia_with_papular_lesions|Alopecia_universalis_congenita|Inborn_genetic_diseases": 2,
    "Alopecia_universalis_congenita|Atrichia_with_papular_lesions|HR-related_disorder|not_provided": 1,
    "Atrichia_with_papular_lesions|Inborn_genetic_diseases|Alopecia_universalis_congenita": 2,
    "Atrichia_with_papular_lesions|Alopecia_universalis_congenita|Inborn_genetic_diseases": 1,
    "Alopecia_universalis_congenita|not_provided|Inborn_genetic_diseases|Atrichia_with_papular_lesions": 2,
    "Inborn_genetic_diseases|not_provided|Alopecia_universalis_congenita|Atrichia_with_papular_lesions": 3,
    "HR-related_disorder|not_provided": 4,
    "not_provided|HR-related_disorder": 1,
    "not_provided|Atrichia_with_papular_lesions": 1,
    "HR-related_disorder": 7,
    "Alopecia_universalis_congenita|Atrichia_with_papular_lesions|not_provided": 4,
    "not_provided|Atrichia_with_papular_lesions|Alopecia_universalis_congenita|not_specified": 1,
    "Atrichia_with_papular_lesions|HR-related_disorder|not_provided|Alopecia_universalis_congenita": 1,
    "Alopecia_universalis_congenita|not_provided|Atrichia_with_papular_lesions|Inborn_genetic_diseases": 1,
    "Atrichia_with_papular_lesions|HR-related_disorder|Alopecia_universalis_congenita|not_provided": 1,
    "not_provided|Atrichia_with_papular_lesions|Alopecia_universalis_congenita|HR-related_disorder": 3,
    "Alopecia_universalis_congenita|Atrichia_with_papular_lesions|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Alopecia_universalis_congenita|Atrichia_with_papular_lesions": 1,
    "Atrichia_with_papular_lesions|Alopecia_universalis_congenita|not_provided|Inborn_genetic_diseases": 1,
    "Hypotrichosis_4": 5,
    "Alopecia_universalis|not_provided|Atrichia_with_papular_lesions": 1,
    "Peripheral_nerve_hyperexcitability_syndrome": 4,
    "Intellectual_developmental_disorder_with_muscle_tone_abnormalities_and_distal_skeletal_defects": 3,
    "LGI3-related_disorder": 6,
    "Intellectual_developmental_disorder_with_muscle_tone_abnormalities_and_distal_skeletal_defects|Peripheral_nerve_hyperexcitability_syndrome": 5,
    "not_provided|Intellectual_developmental_disorder_with_muscle_tone_abnormalities_and_distal_skeletal_defects": 1,
    "not_specified|LGI3-related_disorder": 1,
    "not_provided|LGI3-related_disorder": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2|Osteogenesis_Imperfecta|_Recessive|not_provided": 4,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 11,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2|not_provided": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Interstitial_lung_disease_2": 2,
    "SFTPC-related_disorder": 7,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 1,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_2": 3,
    "Hereditary_pulmonary_alveolar_proteinosis|not_specified|Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Surfactant_metabolism_dysfunction|_pulmonary|_2|not_provided|Interstitial_lung_disease_2": 1,
    "not_provided|Interstitial_lung_disease_2|Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2": 16,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_2|Surfactant_metabolism_dysfunction|_pulmonary|_2": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2|not_provided": 4,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2": 1,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 1,
    "SFTPC-related_disorder|not_provided": 1,
    "Pulmonary_fibrosis|Hereditary_pulmonary_alveolar_proteinosis|not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_2|not_provided|Interstitial_lung_disease_2": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Osteogenesis_Imperfecta|_Recessive|not_provided|not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 2,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2|Pulmonary_fibrosis": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2|not_provided": 3,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2|SFTPC-related_disorder|Interstitial_lung_disease_2|not_provided": 1,
    "SFTPC-related_disorder|Hereditary_pulmonary_alveolar_proteinosis": 2,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Surfactant_metabolism_dysfunction|_pulmonary|_2|SFTPC-related_disorder|Interstitial_lung_disease_2|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2|Inborn_genetic_diseases": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Osteogenesis_Imperfecta|_Recessive|Hereditary_pulmonary_alveolar_proteinosis|not_specified|not_provided|Interstitial_lung_disease_2|Surfactant_metabolism_dysfunction|_pulmonary|_2": 2,
    "Interstitial_lung_disease_2|Surfactant_metabolism_dysfunction|_pulmonary|_2": 1,
    "not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2|not_provided": 1,
    "SFTPC-related_disorder|Hereditary_pulmonary_alveolar_proteinosis|not_specified|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_2|Surfactant_metabolism_dysfunction|_pulmonary|_2|not_provided": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|Surfactant_metabolism_dysfunction|_pulmonary|_2|not_provided": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_2|Interstitial_lung_disease_2": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Surfactant_metabolism_dysfunction|_pulmonary|_2|Osteogenesis_Imperfecta|_Recessive|not_provided|Interstitial_lung_disease_2": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2|not_provided|Interstitial_lung_disease_2": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|not_provided|Osteogenesis_Imperfecta|_Recessive|Interstitial_lung_disease_2": 1,
    "Osteogenesis_Imperfecta|_Recessive|not_provided": 4,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Interstitial_lung_disease_2|Osteogenesis_Imperfecta|_Recessive|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_2|Osteogenesis_Imperfecta|_Recessive|Interstitial_lung_disease_2": 1,
    "not_specified|Osteogenesis_imperfecta_type_13|Pulmonary_Surfactant_Metabolism_Dysfunction|_Dominant|Interstitial_lung_disease_2|Osteogenesis_Imperfecta|_Recessive|not_provided": 1,
    "Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_13|Abnormality_of_the_skeletal_system": 1,
    "not_provided|Osteogenesis_imperfecta_type_13": 16,
    "Osteogenesis_imperfecta|Inborn_genetic_diseases|not_provided": 1,
    "Osteogenesis_imperfecta|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|BMP1-related_disorder": 1,
    "Osteogenesis_imperfecta_type_13|not_provided": 19,
    "Inborn_genetic_diseases|not_provided|BMP1-related_disorder": 1,
    "Osteogenesis_imperfecta_type_13|Inborn_genetic_diseases": 2,
    "Osteogenesis_imperfecta_type_13|not_provided|not_specified": 1,
    "not_provided|BMP1-related_disorder": 6,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_13": 1,
    "BMP1-related_disorder|not_provided": 7,
    "Osteogenesis_imperfecta_type_13": 36,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_13": 2,
    "Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_13|BMP1-related_disorder": 1,
    "not_specified|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_13|BMP1-related_disorder": 1,
    "BMP1-related_disorder": 3,
    "Osteogenesis_imperfecta_type_13|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Inborn_genetic_diseases|Osteogenesis_imperfecta_type_13": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_13|not_specified|not_provided": 1,
    "not_specified|BMP1-related_disorder|not_provided": 1,
    "Osteogenesis_imperfecta_type_13|not_specified|not_provided": 1,
    "Osteogenesis_imperfecta_type_13|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Osteogenesis_imperfecta_type_13|not_provided|Osteogenesis_imperfecta": 1,
    "BMP1-related_disorder|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta_type_13|Osteogenesis_imperfecta|not_provided": 2,
    "not_specified|BMP1-related_disorder": 1,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_13": 2,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_13": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_13": 2,
    "not_provided|Osteogenesis_imperfecta_type_13|Osteogenesis_imperfecta|not_specified": 1,
    "not_provided|Osteogenesis_imperfecta_type_13|BMP1-related_disorder": 1,
    "BMP1-related_disorder|not_provided|Osteogenesis_imperfecta_type_13": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta_type_13": 2,
    "Inborn_genetic_diseases|BMP1-related_disorder|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_13|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_13|not_specified": 1,
    "not_provided|BMP1-related_disorder|Inborn_genetic_diseases|Osteogenesis_imperfecta_type_13": 1,
    "Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_13": 1,
    "BMP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Osteogenesis_imperfecta_type_13|not_specified": 3,
    "not_provided|Osteogenesis_imperfecta_type_13|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_13|not_provided": 1,
    "BMP1-related_disorder|Osteogenesis_imperfecta_type_13|not_provided": 1,
    "Hypermanganesemia_with_dystonia_2": 13,
    "not_provided|SLC39A14-related_disorder": 2,
    "not_specified|Hyperostosis_cranialis_interna|Hypermanganesemia_with_dystonia_2|not_provided": 2,
    "Hyperostosis_cranialis_interna": 3,
    "Hypermanganesemia_with_dystonia_2|Hyperostosis_cranialis_interna|not_provided|not_specified": 1,
    "SLC39A14-related_disorder|not_provided": 3,
    "Hypermanganesemia_with_dystonia_2|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hyperostosis_cranialis_interna|Hypermanganesemia_with_dystonia_2": 1,
    "Hypermanganesemia_with_dystonia_2|Hyperostosis_cranialis_interna": 1,
    "not_provided|SLC39A14-related_disorder|Hyperostosis_cranialis_interna|Hypermanganesemia_with_dystonia_2": 1,
    "Hypermanganesemia_with_dystonia_2|not_provided": 1,
    "CCAR2-related_disorder": 25,
    "not_provided|CCAR2-related_disorder": 2,
    "EGR3-related_disorder": 2,
    "RHOBTB2-related_disorder|not_provided": 12,
    "RHOBTB2-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_64": 26,
    "Developmental_and_epileptic_encephalopathy|_64|not_provided": 6,
    "not_provided|RHOBTB2-related_disorder": 7,
    "not_provided|Developmental_and_epileptic_encephalopathy|_64": 10,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_64": 1,
    "not_provided|Inborn_genetic_diseases|RHOBTB2-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_64|Inborn_genetic_diseases|not_provided": 4,
    "RHOBTB2-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Seizure|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_64|not_provided": 1,
    "RHOBTB2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_64": 2,
    "Developmental_and_epileptic_encephalopathy|_64|Seizure|Inborn_genetic_diseases|not_provided|Rett_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_64|Inborn_genetic_diseases|Dystonic_disorder|Chorea|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_64|not_provided": 1,
    "RHOBTB2-related_disorder|Developmental_and_epileptic_encephalopathy|_64|not_provided": 1,
    "Inborn_genetic_diseases|RHOBTB2-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_64|RHOBTB2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_64|RHOBTB2-related_disorder": 1,
    "TNFRSF10B-related_disorder": 8,
    "not_provided|TNFRSF10B-related_disorder": 1,
    "not_provided|Conotruncal_heart_malformations": 1,
    "NKX2-6-related_disorder": 5,
    "not_provided|Conotruncal_heart_malformations|NKX2-6-related_disorder|not_specified": 1,
    "Conotruncal_heart_malformations|NKX2-6-related_disorder|Inborn_genetic_diseases": 1,
    "Conotruncal_heart_malformations|Cerebral_palsy": 1,
    "Conotruncal_heart_malformations|Persistent_truncus_arteriosus": 1,
    "Conotruncal_heart_malformations|not_provided|not_specified": 1,
    "Conotruncal_heart_malformations|not_provided": 3,
    "not_provided|Conotruncal_heart_malformations|not_specified": 1,
    "NKX2-6-related_disorder|Conotruncal_heart_malformations": 1,
    "Conotruncal_heart_malformations|not_specified|not_provided": 1,
    "not_provided|Conotruncal_heart_malformations|NKX2-6-related_disorder": 2,
    "Charcot-Marie-Tooth_disease_type_1F": 34,
    "Charcot-Marie-Tooth_disease_type_1F|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_2E": 316,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease": 13,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_1F|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2E": 6,
    "not_provided|Charcot-Marie-Tooth_disease_type_2E|not_specified": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2E|not_provided": 3,
    "Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2E|Inborn_genetic_diseases": 14,
    "Charcot-Marie-Tooth_disease_type_2E|not_provided": 14,
    "not_provided|Charcot-Marie-Tooth_disease_type_2E": 25,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2E": 19,
    "Charcot-Marie-Tooth_disease_type_2E|not_specified|not_provided": 2,
    "not_specified|Charcot-Marie-Tooth_disease_type_2E": 9,
    "Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease|Distal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2E|NEFL-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2E|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2E": 3,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F": 1,
    "Charcot-Marie-Tooth_disease_type_2E|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E|not_provided": 2,
    "Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F": 1,
    "Charcot-Marie-Tooth_disease_type_2E|not_specified|not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E": 4,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2E|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_dominant_intermediate_G": 2,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_1F": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2E|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|Hereditary_motor_neuron_disease|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F": 3,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Inborn_genetic_diseases|NEFL-related_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1F": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2E|not_provided": 1,
    "NEFL-related_disorder": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2E|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|NEFL-related_disorder|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease_type_2E|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_2E": 1,
    "NEFL-related_disorder|Charcot-Marie-Tooth_disease_type_2E": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1F|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_1F|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1F": 1,
    "Developmental_disorder|Sensorineural_hearing_loss_disorder|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_1F|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_dominant_intermediate_G": 2,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_axonal|_type_2EE": 1,
    "Charcot-Marie-Tooth_disease_type_2E|not_specified|NEFL-related_disorder|not_provided": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_1F|NEFL-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|NEFL-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1F": 4,
    "not_provided|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|Charcot-Marie-Tooth_disease_type_1F": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease_type_1C|Peripheral_demyelination|Distal_muscle_weakness|Peripheral_neuropathy|Decreased_nerve_conduction_velocity|Hand_muscle_atrophy|Distal_lower_limb_muscle_weakness|Pes_cavus": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2E": 1,
    "Charcot-Marie-Tooth_disease_type_1F|Charcot-Marie-Tooth_disease_type_2E|Charcot-Marie-Tooth_disease|_dominant_intermediate_G|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Hypogonadotropic_hypogonadism_12_with_or_without_anosmia": 12,
    "Hypogonadotropic_hypogonadism_12_with_or_without_anosmia|not_provided": 3,
    "not_provided|Hypogonadotropic_hypogonadism_12_with_or_without_anosmia": 4,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_12_with_or_without_anosmia": 1,
    "DPYSL2-related_disorder": 4,
    "DPYSL2-related_disorder|not_specified": 1,
    "Familial_sleep-related_hypermotor_epilepsy": 134,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 8,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 61,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided": 10,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Intellectual_disability": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided": 3,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 1,
    "CHRNA2-related_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 8,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "not_specified|CHRNA2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "CHRNA2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "not_specified|Benign_familial_infantile_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided": 1,
    "CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_specified": 5,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA2-related_disorder": 3,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Seizures|_benign_familial_infantile|_6|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 3,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases": 3,
    "CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|CHRNA2-related_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 5,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 2,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "CHRNA2-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 3,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA2-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 5,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "not_provided|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Familial_sleep-related_hypermotor_epilepsy": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Seizure|Intellectual_disability": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA2-related_disorder|not_provided": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|CHRNA2-related_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "CHRNA2-related_disorder|Myoclonic_epilepsy|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_4": 1,
    "Familial_sleep-related_hypermotor_epilepsy|not_provided": 7,
    "EPHX2-related_disorder": 8,
    "CLU-related_disorder": 6,
    "Alzheimer_disease|not_provided": 14,
    "CLU-related_disorder|not_provided": 1,
    "not_provided|CLU-related_disorder": 1,
    "not_specified|SCARA3-related_disorder": 1,
    "not_provided|SCARA3-related_disorder": 1,
    "Roberts-SC_phocomelia_syndrome": 84,
    "Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome": 60,
    "ESCO2-related_disorder|not_provided": 2,
    "Juberg-Hayward_syndrome|Roberts-SC_phocomelia_syndrome|ESCO2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Juberg-Hayward_syndrome|Roberts-SC_phocomelia_syndrome|not_provided": 1,
    "ESCO2-related_disorder": 2,
    "Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|not_provided": 15,
    "Juberg-Hayward_syndrome|Roberts-SC_phocomelia_syndrome|not_provided": 14,
    "Roberts-SC_phocomelia_syndrome|not_provided|not_specified": 1,
    "not_provided|Roberts-SC_phocomelia_syndrome|Inborn_genetic_diseases": 2,
    "Juberg-Hayward_syndrome|Roberts-SC_phocomelia_syndrome|Inborn_genetic_diseases": 3,
    "Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|not_specified|not_provided": 2,
    "Roberts-SC_phocomelia_syndrome|not_provided": 49,
    "ESCO2-related_disorder|Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|not_provided": 1,
    "Roberts-SC_phocomelia_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|ESCO2-related_disorder|not_specified": 1,
    "Roberts-SC_phocomelia_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Roberts-SC_phocomelia_syndrome|ESCO2-related_disorder": 1,
    "Roberts-SC_phocomelia_syndrome|ESCO2-related_disorder|not_provided": 2,
    "Roberts-SC_phocomelia_syndrome|ESCO2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "ESCO2-related_disorder|Roberts-SC_phocomelia_syndrome|not_provided|Juberg-Hayward_syndrome": 1,
    "not_provided|ESCO2-related_disorder": 2,
    "Roberts-SC_phocomelia_syndrome|Inborn_genetic_diseases": 2,
    "Roberts-SC_phocomelia_syndrome|not_provided|Juberg-Hayward_syndrome": 1,
    "Roberts-SC_phocomelia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Roberts-SC_phocomelia_syndrome|ESCO2-related_disorder|not_specified|not_provided": 1,
    "Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Roberts-SC_phocomelia_syndrome": 7,
    "not_provided|Roberts-SC_phocomelia_syndrome|ESCO2-related_disorder|not_specified": 1,
    "Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|ESCO2-related_disorder|not_specified|not_provided": 1,
    "ESCO2-related_disorder|Roberts-SC_phocomelia_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Roberts-SC_phocomelia_syndrome|not_provided": 1,
    "Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Juberg-Hayward_syndrome|Roberts-SC_phocomelia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome": 1,
    "not_provided|Juberg-Hayward_syndrome|Roberts-SC_phocomelia_syndrome": 2,
    "not_provided|Roberts-SC_phocomelia_syndrome|Juberg-Hayward_syndrome|ESCO2-related_disorder": 1,
    "not_provided|Roberts-SC_phocomelia_syndrome|not_specified": 3,
    "Inborn_genetic_diseases|ESCO2-related_disorder": 1,
    "not_provided|Roberts-SC_phocomelia_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Tyrosinase-positive_oculocutaneous_albinism": 66,
    "Congenital_cerebellar_hypoplasia|Corpus_callosum|_agenesis_of|Hydrocephalus|Arthrogryposis_multiplex_congenita|Multicystic_kidney_dysplasia": 1,
    "not_provided|EXTL3-related_disorder": 7,
    "Immunoskeletal_dysplasia_with_neurodevelopmental_abnormalities|Inborn_genetic_diseases|not_provided": 2,
    "EXTL3-related_disorder": 2,
    "Immunoskeletal_dysplasia_with_neurodevelopmental_abnormalities": 2,
    "not_provided|Immunoskeletal_dysplasia_with_neurodevelopmental_abnormalities": 4,
    "Immunoskeletal_dysplasia_with_neurodevelopmental_abnormalities|not_provided": 1,
    "EXTL3-related_disorder|not_provided": 2,
    "Familial_meningioma|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Immunoskeletal_dysplasia_with_neurodevelopmental_abnormalities": 1,
    "Inborn_genetic_diseases|not_provided|Immunoskeletal_dysplasia_with_neurodevelopmental_abnormalities": 1,
    "Trichothiodystrophy_6|_nonphotosensitive": 3,
    "not_provided|Trichothiodystrophy_6|_nonphotosensitive": 1,
    "GTF2E2-related_disorder|not_provided": 3,
    "not_provided|GTF2E2-related_disorder": 2,
    "Hemolytic_anemia_due_to_glutathione_reductase_deficiency": 47,
    "Hemolytic_anemia_due_to_glutathione_reductase_deficiency|not_provided|not_specified": 3,
    "Hemolytic_anemia_due_to_glutathione_reductase_deficiency|GSR-related_disorder|not_provided": 2,
    "not_provided|Hemolytic_anemia_due_to_glutathione_reductase_deficiency|not_specified": 3,
    "not_provided|GSR-related_disorder": 2,
    "not_specified|Hemolytic_anemia_due_to_glutathione_reductase_deficiency": 4,
    "GSR-related_disorder|not_provided": 3,
    "not_provided|GSR-related_disorder|Hemolytic_anemia_due_to_glutathione_reductase_deficiency": 2,
    "GSR-related_disorder": 4,
    "GSR-related_disorder|Hemolytic_anemia_due_to_glutathione_reductase_deficiency|not_provided": 5,
    "not_provided|Hemolytic_anemia_due_to_glutathione_reductase_deficiency": 5,
    "Hemolytic_anemia_due_to_glutathione_reductase_deficiency|not_provided": 4,
    "Hemolytic_anemia_due_to_glutathione_reductase_deficiency|not_specified": 3,
    "not_specified|Hemolytic_anemia_due_to_glutathione_reductase_deficiency|GSR-related_disorder": 1,
    "not_specified|Hemolytic_anemia_due_to_glutathione_reductase_deficiency|not_provided": 1,
    "Spermatogenic_failure_25|not_provided": 5,
    "not_provided|TEX15-related_disorder": 7,
    "not_provided|Non-obstructive_azoospermia": 1,
    "Spermatogenic_failure_25": 25,
    "TEX15-related_disorder|not_provided": 5,
    "TEX15-related_disorder": 20,
    "TEX15-related_disorder|Spermatogenic_failure_25": 1,
    "Non-obstructive_azoospermia|not_provided|TEX15-related_disorder": 1,
    "not_specified|Spermatogenic_failure_25": 4,
    "not_provided|Spermatogenic_failure_25": 2,
    "TEX15-related_disorder|Spermatogenic_failure_25|not_provided": 1,
    "Spermatogenic_failure_25|not_specified|not_provided": 1,
    "not_provided|TEX15-related_disorder|Spermatogenic_failure_25": 1,
    "Spermatogenic_failure_25|Oligosynaptic_infertility": 1,
    "Spermatogenic_failure_25|not_specified": 1,
    "Werner_syndrome": 3300,
    "not_provided|Werner_syndrome": 55,
    "not_specified|Werner_syndrome": 9,
    "Inborn_genetic_diseases|Werner_syndrome": 42,
    "Werner_syndrome|not_specified": 17,
    "Werner_syndrome|not_provided|Wiskott-Aldrich_syndrome": 2,
    "not_specified|not_provided|Werner_syndrome": 6,
    "WRN-related_disorder|Werner_syndrome|Wiskott-Aldrich_syndrome|not_provided|not_specified": 1,
    "Werner_syndrome|not_provided": 46,
    "not_specified|not_provided|Wiskott-Aldrich_syndrome|Werner_syndrome": 4,
    "Ovarian_cancer|Werner_syndrome": 4,
    "Werner_syndrome|WRN-related_disorder": 19,
    "not_provided|not_specified|Wiskott-Aldrich_syndrome|Werner_syndrome": 1,
    "not_provided|not_specified|Werner_syndrome": 2,
    "Wiskott-Aldrich_syndrome|not_provided|Werner_syndrome|not_specified": 3,
    "Werner_syndrome|Inborn_genetic_diseases": 48,
    "WRN-related_disorder|Werner_syndrome": 13,
    "not_provided|Wiskott-Aldrich_syndrome|Werner_syndrome|not_specified": 1,
    "WRN-related_disorder|Werner_syndrome|not_specified": 1,
    "Progressive_pulmonary_failure": 1,
    "not_provided|Werner_syndrome|WRN-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|Werner_syndrome": 1,
    "WRN-related_disorder|Werner_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Werner_syndrome|Mask-like_facies|Type_2_diabetes_mellitus|Cataract|Decreased_body_weight|Convex_nasal_ridge|Short_stature": 1,
    "Werner_syndrome|Inborn_genetic_diseases|WRN-related_disorder": 1,
    "not_provided|Werner_syndrome|Inborn_genetic_diseases": 3,
    "WRN-related_disorder": 4,
    "Inborn_genetic_diseases|not_specified|not_provided|Werner_syndrome": 3,
    "not_specified|not_provided|Wiskott-Aldrich_syndrome|Werner_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Medulloblastoma|Werner_syndrome": 1,
    "Ovarian_cancer|Inborn_genetic_diseases|Werner_syndrome": 1,
    "not_provided|Werner_syndrome|Wiskott-Aldrich_syndrome": 1,
    "not_provided|Wiskott-Aldrich_syndrome|not_specified|Werner_syndrome": 1,
    "Werner_syndrome|not_provided|WRN-related_disorder": 3,
    "WRN-related_disorder|Wiskott-Aldrich_syndrome|Werner_syndrome": 1,
    "Werner_syndrome|WRN-related_disorder|not_provided|not_specified": 1,
    "WRN-related_disorder|Werner_syndrome|Inborn_genetic_diseases": 1,
    "Werner_syndrome|WRN-related_disorder|not_provided": 1,
    "Werner_syndrome|not_provided|not_specified": 4,
    "Wiskott-Aldrich_syndrome|Werner_syndrome|not_specified|not_provided": 1,
    "WRN-related_disorder|not_provided|Werner_syndrome": 3,
    "not_specified|Werner_syndrome|not_provided|Wiskott-Aldrich_syndrome": 1,
    "Werner_syndrome|not_specified|not_provided|Wiskott-Aldrich_syndrome": 1,
    "Wiskott-Aldrich_syndrome|Werner_syndrome|not_specified": 1,
    "WRN-related_disorder|not_specified|not_provided|Werner_syndrome": 1,
    "Werner_syndrome|not_specified|not_provided": 2,
    "Werner_syndrome|Inborn_genetic_diseases|Ovarian_cancer": 1,
    "Werner_syndrome|not_specified|not_provided|WRN-related_disorder": 1,
    "Hereditary_cancer|Inborn_genetic_diseases|Werner_syndrome": 1,
    "WRN-related_disorder|Inborn_genetic_diseases|Werner_syndrome": 1,
    "Ovarian_cancer|Werner_syndrome|WRN-related_disorder": 1,
    "Werner_syndrome|Ovarian_cancer": 3,
    "Werner_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "WRN-related_disorder|Werner_syndrome|not_provided": 1,
    "Werner_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Werner_syndrome": 3,
    "not_specified|Werner_syndrome|Wiskott-Aldrich_syndrome": 1,
    "Werner_syndrome|not_provided|Ovarian_cancer|not_specified": 1,
    "WRN-related_disorder|not_specified|not_provided|Wiskott-Aldrich_syndrome|Werner_syndrome": 1,
    "Werner_syndrome|Wiskott-Aldrich_syndrome": 1,
    "Inborn_genetic_diseases|Werner_syndrome|not_provided": 1,
    "Wiskott-Aldrich_syndrome|not_specified|Werner_syndrome|not_provided": 2,
    "not_specified|Wiskott-Aldrich_syndrome|not_provided|Werner_syndrome": 1,
    "not_specified|Werner_syndrome|Wiskott-Aldrich_syndrome|not_provided": 1,
    "WRN-related_disorder|not_provided|Werner_syndrome|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Werner_syndrome": 1,
    "not_provided|Werner_syndrome|not_specified": 1,
    "Werner_syndrome|not_provided|Wiskott-Aldrich_syndrome|not_specified": 1,
    "Wiskott-Aldrich_syndrome|not_specified|not_provided|Werner_syndrome": 1,
    "not_specified|Wiskott-Aldrich_syndrome|Werner_syndrome|not_provided": 1,
    "WRN-related_disorder|Werner_syndrome|not_specified|not_provided": 1,
    "NRG1-related_disorder|not_provided": 5,
    "NRG1-related_disorder": 15,
    "Schizophrenia_6|NRG1-related_disorder|not_specified|not_provided": 1,
    "not_provided|NRG1-related_disorder": 3,
    "not_provided|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome": 2,
    "Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome": 11,
    "not_provided|TTI2-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome": 2,
    "Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome|Microcephaly": 1,
    "TTI2-related_disorder|not_provided": 2,
    "TTI2-related_disorder": 3,
    "not_provided|TTI2-related_disorder": 1,
    "Inborn_genetic_diseases|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome": 1,
    "not_provided|TTI2-related_disorder|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome": 1,
    "TTI2-related_disorder|not_provided|Severe_intellectual_disability-short_stature-behavioral_abnormalities-facial_dysmorphism_syndrome": 1,
    "Spermatogenic_failure_79": 3,
    "Hereditary_spastic_paraplegia_18": 11,
    "Inborn_genetic_diseases|not_specified|Spastic_paraplegia": 4,
    "ERLIN2-related_disorder": 1,
    "Hereditary_spastic_paraplegia_18|Spastic_paraplegia|_autosomal_dominant": 1,
    "Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia": 2,
    "Spastic_paraparesis|Spastic_paraplegia": 1,
    "Spastic_paraplegia_18a|_autosomal_dominant": 1,
    "Spastic_paraplegia|ERLIN2-related_disorder": 1,
    "Spastic_paraplegia_18a|_autosomal_dominant|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Spastic_paraplegia_18a|_autosomal_dominant": 1,
    "not_provided|ERLIN2-related_disorder|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|ERLIN2-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Spastic_paraplegia": 3,
    "not_provided|not_specified|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "ERLIN2-related_disorder|not_specified|not_provided|Spastic_paraplegia": 1,
    "not_specified|not_provided|Spastic_paraplegia": 12,
    "Hereditary_spastic_paraplegia_18|Spastic_paraplegia": 1,
    "PLPBP-related_disorder": 2,
    "Epilepsy|_early-onset|_vitamin_B6-dependent": 16,
    "not_provided|Epilepsy|_early-onset|_vitamin_B6-dependent": 9,
    "PLPBP-related_disorder|not_provided": 3,
    "Epilepsy|_early-onset|_vitamin_B6-dependent|not_provided|PLPBP-related_disorder|not_specified": 1,
    "Epilepsy|_early-onset|_vitamin_B6-dependent|not_provided": 6,
    "BRF2-related_disorder": 1,
    "not_specified|Obesity|not_provided": 3,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency": 115,
    "not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency": 26,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_provided": 37,
    "Inborn_genetic_diseases|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency": 2,
    "STAR-related_disorder|not_provided": 2,
    "not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|Inborn_genetic_diseases": 1,
    "Syndactyly-telecanthus-anogenital_and_renal_malformations_syndrome|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_provided": 1,
    "STAR-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency": 1,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|Syndactyly-telecanthus-anogenital_and_renal_malformations_syndrome|not_provided": 1,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_provided|STAR-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_provided": 1,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_provided|not_specified|STAR-related_disorder": 1,
    "not_provided|not_specified|STAR-related_disorder": 1,
    "not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_specified": 1,
    "not_provided|STAR-related_disorder": 2,
    "not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|STAR-related_disorder": 2,
    "STAR-related_disorder|not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency": 1,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|Inborn_genetic_diseases": 1,
    "Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|Inborn_genetic_diseases|not_provided": 1,
    "STAR-related_disorder|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|not_provided": 2,
    "not_provided|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency|STAR-related_disorder|not_specified": 1,
    "STAR-related_disorder|Congenital_lipoid_adrenal_hyperplasia_due_to_STAR_deficency": 1,
    "Complex_neurodevelopmental_disorder|Cryptorchidism|Oligohydramnios|Intellectual_disability|Patent_ductus_arteriosus_after_premature_birth|Perimembranous_ventricular_septal_defect|Generalized_hypotonia|Mitral_stenosis|Strabismus|Constipation|Penile_hypospadias|Hemivertebrae|Hydroureter|Abnormal_facial_shape|Inguinal_hernia|Feeding_difficulties|Bicuspid_aortic_valve|Triphalangeal_thumb|Neurodevelopmental_delay|Fetal_pyelectasis|not_provided": 1,
    "Global_developmental_delay|FICUS_SYNDROME": 1,
    "Hereditary_spastic_paraplegia_54|not_specified": 3,
    "Hereditary_spastic_paraplegia_54": 160,
    "Hereditary_spastic_paraplegia_54|not_provided": 6,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_54|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_54|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_54|Inborn_genetic_diseases": 12,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_54": 13,
    "Hereditary_spastic_paraplegia_54|DDHD2-related_disorder": 2,
    "not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_54": 1,
    "not_specified|Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia|not_provided": 3,
    "not_provided|Hereditary_spastic_paraplegia_54": 5,
    "Hereditary_spastic_paraplegia_54|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_spastic_paraplegia_54": 3,
    "Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_54": 1,
    "Hereditary_spastic_paraplegia_54|not_specified|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_54|Senior-Loken_syndrome_6": 1,
    "Hereditary_spastic_paraplegia_54|not_specified|not_provided": 3,
    "DDHD2-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_54": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_54|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_54": 1,
    "Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia|not_provided": 2,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_54": 1,
    "Hereditary_spastic_paraplegia_54|Hereditary_spastic_paraplegia|DDHD2-related_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_54|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_54": 1,
    "Senior-Loken_syndrome_6": 2,
    "DDHD2-related_disorder|Hereditary_spastic_paraplegia_54": 1,
    "Inborn_genetic_diseases|Global_developmental_delay|Obesity|Generalized_epilepsy|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_54": 1,
    "Hereditary_spastic_paraplegia_54|not_provided|Inborn_genetic_diseases": 1,
    "NSD3-related_disorder": 9,
    "Nut_midline_carcinoma": 1,
    "NSD3-related_disorder|not_provided": 1,
    "Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Trigonocephaly_1": 4,
    "Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1": 2,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Trigonocephaly_1": 5,
    "Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Trigonocephaly_1": 17,
    "Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Trigonocephaly_1": 2,
    "Osteoglophonic_dysplasia|Pfeiffer_syndrome|Hypogonadism_with_anosmia|Interfrontal_craniofaciosynostosis|Craniosynostosis_syndrome": 1,
    "Craniosynostosis_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 3,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 9,
    "Craniosynostosis_syndrome|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1": 4,
    "Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Craniosynostosis_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|not_provided": 1,
    "FGFR1-related_disorder|Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|not_provided": 1,
    "Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 5,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia": 7,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1": 1,
    "FGFR1-related_disorder": 18,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome": 4,
    "Craniosynostosis_syndrome|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Craniosynostosis_syndrome|not_provided|not_specified|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia": 1,
    "Craniosynostosis_syndrome|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Trigonocephaly_1": 1,
    "Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Trigonocephaly_1|Craniosynostosis_syndrome": 3,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|not_provided|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Osteoglophonic_dysplasia": 1,
    "Trigonocephaly_1|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia": 1,
    "Trigonocephaly_1|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Osteoglophonic_dysplasia": 1,
    "Trigonocephaly_1|Craniosynostosis_syndrome|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Osteoglophonic_dysplasia|Trigonocephaly_1|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia": 8,
    "Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome": 2,
    "Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|not_provided|Infertility_disorder": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Craniosynostosis_syndrome|FGFR1-related_disorder|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 253,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 129,
    "spinal_cord_mass": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 100,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Pfeiffer_syndrome": 1,
    "Pfeiffer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 2,
    "not_provided|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Osteoglophonic_dysplasia": 1,
    "Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia": 1,
    "Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 24,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 3,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_specified": 6,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Craniosynostosis_syndrome|not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided": 13,
    "Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "FGFR1-related_disorder|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|not_provided": 1,
    "Jackson-Weiss_syndrome": 2,
    "not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia": 2,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_specified|Craniosynostosis_syndrome|not_provided|Osteoglophonic_dysplasia|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided": 3,
    "not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome": 1,
    "Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia": 2,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided": 8,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|not_provided": 1,
    "Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Craniosynostosis_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 3,
    "Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Craniosynostosis_syndrome|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia": 4,
    "FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis": 1,
    "Pfeiffer_syndrome_type_1": 1,
    "FGFR1-related_disorder|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 3,
    "FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 4,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|not_specified|not_provided|Trigonocephaly_1|Osteoglophonic_dysplasia": 2,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Trigonocephaly_1|Jackson-Weiss_syndrome": 1,
    "not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Martsolf_syndrome_1": 1,
    "Hartsfield-Bixler-Demyer_syndrome": 19,
    "Hypogonadotropic_hypogonadism_2_with_anosmia": 7,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 6,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Trigonocephaly_1|Jackson-Weiss_syndrome|Pfeiffer_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "Inborn_genetic_diseases|FGFR1-related_disorder|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_anosmia|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|FGFR1-related_disorder|not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|not_provided": 2,
    "Delayed_puberty|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Craniosynostosis_syndrome|not_provided|Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "not_provided|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Inborn_genetic_diseases|FGFR1-related_disorder|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism_2_with_anosmia": 1,
    "not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 11,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|FGFR1-related_craniosynostosis_syndrome|Pfeiffer_syndrome": 1,
    "FGFR1-related_disorder|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided": 2,
    "not_provided|FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "not_provided|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Trigonocephaly_1": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder": 2,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|not_provided|FGFR1-related_disorder|Semilobar_holoprosencephaly": 1,
    "Pilomyxoid_astrocytoma|Encephalocraniocutaneous_lipomatosis": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Delayed_puberty": 2,
    "FGFR1-related_disorder|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|Hartsfield-Bixler-Demyer_syndrome|Cerebellar_vermis_hypoplasia": 1,
    "Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Craniosynostosis_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|not_provided": 1,
    "Delayed_puberty|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|See_cases|Hypogonadotropic_hypogonadism|Pfeiffer_syndrome|not_provided": 1,
    "not_specified|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_anosmia|not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis": 2,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Pilomyxoid_astrocytoma|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified": 1,
    "not_provided|not_specified|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Inborn_genetic_diseases|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Encephalocraniocutaneous_lipomatosis": 1,
    "Rosette-forming_glioneuronal_tumor|Encephalocraniocutaneous_lipomatosis": 1,
    "FGFR1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hartsfield-Bixler-Demyer_syndrome": 3,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Inborn_genetic_diseases": 5,
    "Pfeiffer_syndrome|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|not_provided": 1,
    "Osteoglophonic_dysplasia|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 9,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|not_provided|Pfeiffer_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified": 5,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Trigonocephaly_1": 1,
    "Osteoglophonic_dysplasia": 4,
    "Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis": 1,
    "Hypogonadotropic_hypogonadism_2_with_anosmia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Inborn_genetic_diseases|Pfeiffer_syndrome|not_provided|Craniosynostosis_syndrome": 1,
    "Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Jackson-Weiss_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis": 1,
    "not_provided|not_specified|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Pfeiffer_syndrome|Osteoglophonic_dysplasia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome": 1,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|not_specified|Pfeiffer_syndrome|Craniosynostosis_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Craniosynostosis|_nonspecific|not_provided": 1,
    "FGFR1-related_disorder|Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Inborn_genetic_diseases|not_provided": 1,
    "Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|FGFR1-related_disorder": 1,
    "not_specified|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|not_specified": 1,
    "Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|not_provided": 1,
    "Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis": 2,
    "not_specified|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|FGFR1-related_disorder": 1,
    "Pfeiffer_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Trigonocephaly_1|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_2_with_anosmia|not_provided": 1,
    "Pfeiffer_syndrome|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|FGFR1-related_disorder|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia": 1,
    "FGFR1-related_disorder|not_provided|Hypogonadotropic_hypogonadism_2_with_anosmia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|not_provided|Pfeiffer_syndrome|Delayed_puberty": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified|not_provided|FGFR1-related_disorder|Pfeiffer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism_2_with_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Inborn_genetic_diseases": 1,
    "Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|FGFR1-related_disorder": 1,
    "Trigonocephaly_1|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|not_specified|FGFR1-related_disorder|not_provided": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|FGFR1-related_disorder": 2,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Delayed_puberty": 1,
    "Jackson-Weiss_syndrome|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Trigonocephaly_1|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|FGFR1-related_disorder|not_provided": 1,
    "Lobar_holoprosencephaly|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome": 1,
    "Craniosynostosis_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hypogonadotropic_hypogonadism": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia": 2,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|Inborn_genetic_diseases": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|FGFR1-related_disorder|not_provided": 1,
    "Craniosynostosis_syndrome|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_specified|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|FGFR1-related_disorder|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Pfeiffer_syndrome": 7,
    "Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|not_specified|Pfeiffer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis": 1,
    "Pfeiffer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome": 1,
    "See_cases|not_provided|not_specified": 2,
    "Pfeiffer_syndrome|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Osteoglophonic_dysplasia|Inborn_genetic_diseases|Craniosynostosis_syndrome": 1,
    "not_provided|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia": 1,
    "Mendelian_syndromes_with_cleft_lip/palate|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Trigonocephaly_1": 2,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided": 2,
    "Hartsfield-Bixler-Demyer_syndrome|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis": 1,
    "Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|not_provided|Pfeiffer_syndrome|Trigonocephaly_1": 1,
    "Pfeiffer_syndrome|not_provided": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Craniosynostosis_syndrome|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified|Craniosynostosis_syndrome|not_provided|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "FGFR1-related_disorder|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified|not_provided": 1,
    "Pfeiffer_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|FGFR1-related_disorder": 1,
    "not_provided|FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified|Trigonocephaly_1|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Craniosynostosis_syndrome": 1,
    "Hartsfield-Bixler-Demyer_syndrome|not_provided|Trigonocephaly_1|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|Osteoglophonic_dysplasia|Craniosynostosis_syndrome": 1,
    "FGFR1-related_disorder|not_specified|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "Trigonocephaly_1|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|See_cases": 1,
    "Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Pfeiffer_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|FGFR1-related_disorder|Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome": 1,
    "Encephalocraniocutaneous_lipomatosis|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia": 1,
    "FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|not_provided|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis": 1,
    "not_provided|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia": 1,
    "Pfeiffer_syndrome|FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_specified": 1,
    "FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Pfeiffer_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Inborn_genetic_diseases|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|not_provided": 1,
    "not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis": 1,
    "Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "FGFR1-related_disorder|not_provided|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Inborn_genetic_diseases": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome": 1,
    "Osteoglophonic_dysplasia|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|not_specified|not_provided": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia": 1,
    "not_provided|FGFR1-related_disorder|Osteoglophonic_dysplasia|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Trigonocephaly_1|Craniosynostosis_syndrome": 1,
    "not_provided|Encephalocraniocutaneous_lipomatosis": 1,
    "FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided": 1,
    "not_provided|Pfeiffer_syndrome|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Encephalocraniocutaneous_lipomatosis|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Inborn_genetic_diseases": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|Jackson-Weiss_syndrome|Trigonocephaly_1": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia": 1,
    "Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Osteoglophonic_dysplasia|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1": 1,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Encephalocraniocutaneous_lipomatosis|Trigonocephaly_1|Osteoglophonic_dysplasia": 1,
    "Trigonocephaly_1|Pfeiffer_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|FGFR1-related_disorder|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|not_specified": 1,
    "not_provided|FGFR1-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Pfeiffer_syndrome|not_provided|Trigonocephaly_1": 1,
    "not_specified|not_provided|Osteoglophonic_dysplasia|FGFR1-related_disorder|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome": 1,
    "not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Jackson-Weiss_syndrome|Osteoglophonic_dysplasia|Encephalocraniocutaneous_lipomatosis": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Hartsfield-Bixler-Demyer_syndrome|Trigonocephaly_1|Encephalocraniocutaneous_lipomatosis|Osteoglophonic_dysplasia|not_provided": 1,
    "FGFR1-related_disorder|not_provided": 1,
    "not_provided|Jackson-Weiss_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Encephalocraniocutaneous_lipomatosis|Pfeiffer_syndrome|Trigonocephaly_1|Hartsfield-Bixler-Demyer_syndrome|Osteoglophonic_dysplasia|not_specified": 1,
    "Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Craniosynostosis_syndrome": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Craniosynostosis_syndrome|Osteoglophonic_dysplasia|Trigonocephaly_1": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|not_provided|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "Trigonocephaly_1|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided": 1,
    "Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|not_provided": 1,
    "Craniosynostosis_syndrome|Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Osteoglophonic_dysplasia": 1,
    "Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|not_provided|Craniosynostosis_syndrome": 1,
    "Trigonocephaly_1|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|Osteoglophonic_dysplasia|Craniosynostosis_syndrome|not_specified": 1,
    "Hypogonadotropic_hypogonadism_2_with_or_without_anosmia|not_provided|Osteoglophonic_dysplasia|Trigonocephaly_1|Craniosynostosis_syndrome": 2,
    "not_specified|Seizure": 2,
    "Seizure|not_specified": 2,
    "Cone-rod_dystrophy_9": 37,
    "not_provided|not_specified|Cone-rod_dystrophy_9": 2,
    "Cone-rod_dystrophy_9|not_specified|not_provided": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_9|ADAM9-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Cone-rod_dystrophy_9": 1,
    "Cone-rod_dystrophy_9|Cone-rod_dystrophy": 2,
    "not_provided|Cone-rod_dystrophy_9|Cone-rod_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_9": 17,
    "not_provided|ADAM9-related_disorder": 3,
    "not_provided|Cone-rod_dystrophy_9|ADAM9-related_disorder": 1,
    "ADAM9-related_disorder|not_provided": 3,
    "Cone-rod_dystrophy_9|not_provided": 8,
    "not_provided|Cone-Rod_Dystrophy|_Recessive": 12,
    "not_specified|not_provided|Cone-rod_dystrophy_9": 1,
    "not_provided|Cone-rod_dystrophy_9|Cone-Rod_Dystrophy|_Recessive|not_specified": 1,
    "ADAM9-related_disorder": 1,
    "not_provided|ADAM9-related_disorder|Cone-rod_dystrophy_9": 1,
    "Cone-rod_dystrophy_9|Inborn_genetic_diseases|not_provided": 1,
    "Cone-rod_dystrophy_9|not_provided|Inborn_genetic_diseases": 2,
    "Cone-rod_dystrophy_9|ADAM9-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy_9": 1,
    "Cone-Rod_Dystrophy|_Recessive": 13,
    "Hereditary_spherocytosis_type_1|Spherocytosis": 59,
    "Spherocytosis|Hereditary_spherocytosis_type_1": 35,
    "Hereditary_spherocytosis_type_1|Spherocytosis|not_provided": 20,
    "Hereditary_spherocytosis_type_1": 443,
    "Spherocytosis|_Dominant": 10,
    "not_provided|Spherocytosis|_Dominant|Hereditary_spherocytosis_type_1": 1,
    "Hereditary_spherocytosis_type_1|not_provided": 58,
    "not_provided|Hereditary_spherocytosis_type_1|Spherocytosis": 22,
    "ANK1-related_disorder": 37,
    "not_provided|ANK1-related_disorder|Hereditary_spherocytosis_type_1|Spherocytosis": 1,
    "ANK1-related_disorder|Hereditary_spherocytosis_type_1": 3,
    "Hereditary_spherocytosis_type_1|not_specified|not_provided": 3,
    "not_provided|Hereditary_spherocytosis_type_1": 48,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_1": 17,
    "Spherocytosis|Hereditary_spherocytosis_type_1|not_provided": 1,
    "ANK1-related_disorder|Hereditary_spherocytosis_type_1|not_provided": 2,
    "Spherocytosis|not_provided|not_specified|Hereditary_spherocytosis_type_1": 6,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_1|Spherocytosis": 4,
    "not_provided|Hereditary_spherocytosis_type_1|ANK1-related_disorder": 3,
    "Hereditary_spherocytosis_type_1|ANK1-related_disorder": 5,
    "Hemolytic_anemia|Hereditary_spherocytosis_type_1": 1,
    "not_provided|Hereditary_spherocytosis": 1,
    "Hereditary_spherocytosis_type_1|Inborn_genetic_diseases": 10,
    "Hereditary_spherocytosis_type_1|Inborn_genetic_diseases|Spherocytosis": 3,
    "Hereditary_spherocytosis_type_1|Spherocytosis|Inborn_genetic_diseases": 3,
    "not_provided|Hereditary_spherocytosis_type_1|not_specified": 2,
    "Hereditary_spherocytosis_type_1|not_provided|Spherocytosis": 4,
    "Spherocytosis|Inborn_genetic_diseases|Hereditary_spherocytosis_type_1": 2,
    "Spherocytosis|not_specified|Hereditary_spherocytosis_type_1|not_provided": 3,
    "not_provided|Hereditary_spherocytosis_type_1|Inborn_genetic_diseases": 3,
    "ANK1-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_spherocytosis_type_1|Spherocytosis": 1,
    "not_provided|ANK1-related_disorder": 3,
    "Spherocytosis|not_specified|not_provided|Hereditary_spherocytosis_type_1": 4,
    "Hereditary_spherocytosis_type_1|Inborn_genetic_diseases|not_provided": 2,
    "Hereditary_spherocytosis_type_1|not_provided|Inborn_genetic_diseases": 3,
    "ANK1-related_disorder|not_provided": 3,
    "Hereditary_spherocytosis_type_1|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_1|not_provided|Spherocytosis|ANK1-related_disorder": 1,
    "Spherocytosis|Hereditary_spherocytosis_type_1|Inborn_genetic_diseases|not_provided": 1,
    "ANK1-related_disorder|Hereditary_spherocytosis_type_1|Spherocytosis|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_1|not_provided": 2,
    "not_specified|Hereditary_spherocytosis_type_1|not_provided|Spherocytosis": 2,
    "not_provided|ANK1-related_disorder|Hereditary_spherocytosis_type_1": 3,
    "Spherocytosis|not_provided|Hereditary_spherocytosis_type_1|not_specified": 2,
    "Hereditary_spherocytosis": 11,
    "Hereditary_spherocytosis_type_1|not_provided|Spherocytosis|Inborn_genetic_diseases": 1,
    "Hereditary_spherocytosis_type_1|not_provided|Hereditary_spherocytosis": 1,
    "Spherocytosis|ANK1-related_disorder|Hereditary_spherocytosis_type_1|not_provided": 1,
    "Spherocytosis|not_provided|Hereditary_spherocytosis_type_1": 4,
    "Inborn_genetic_diseases|not_provided|Hereditary_spherocytosis_type_1": 5,
    "not_provided|Inborn_genetic_diseases|Hereditary_spherocytosis_type_1": 2,
    "Spherocytosis|Hereditary_spherocytosis_type_1|not_provided|ANK1-related_disorder": 1,
    "not_provided|not_specified|Hereditary_spherocytosis_type_1|Spherocytosis": 1,
    "Hereditary_spherocytosis_type_1|Spherocytosis|not_specified|not_provided": 1,
    "ANK1-related_disorder|Hereditary_spherocytosis_type_1|not_provided|Spherocytosis": 1,
    "Hereditary_spherocytosis_type_1|not_provided|ANK1-related_disorder": 1,
    "ANK1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Spherocytosis|Hereditary_spherocytosis_type_1": 1,
    "not_provided|Spherocytosis|Hereditary_spherocytosis_type_1|not_specified": 1,
    "not_specified|not_provided|Hereditary_spherocytosis_type_1|Spherocytosis": 1,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_1|Spherocytosis|not_provided": 1,
    "Hereditary_spherocytosis_type_1|Anemia": 1,
    "not_provided|Spherocytosis|not_specified|Hereditary_spherocytosis_type_1": 1,
    "Hereditary_spherocytosis_type_1|Spherocytosis|ANK1-related_disorder": 1,
    "Hereditary_spherocytosis_type_1|not_provided|SPHEROCYTOSIS|_TYPE_1|_AUTOSOMAL_RECESSIVE": 1,
    "Inborn_genetic_diseases|ANK1-related_disorder|not_provided": 1,
    "Hereditary_spherocytosis_type_1|Hereditary_spherocytosis": 1,
    "not_provided|Hereditary_spherocytosis_type_1|Spherocytosis|not_specified": 2,
    "Hereditary_spherocytosis_type_1|Spherocytosis|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Spherocytosis|Hereditary_spherocytosis_type_1|not_provided": 1,
    "Hereditary_spherocytosis_type_1|Spherocytosis|_Dominant|Inborn_genetic_diseases": 1,
    "Immunodeficiency_62|not_provided|Hereditary_spherocytosis_type_1|Spherocytosis|ANK1-related_disorder": 1,
    "Hereditary_spherocytosis|not_provided|Hereditary_spherocytosis_type_1": 1,
    "See_cases|not_provided|Hereditary_spherocytosis_type_1|ANK1-related_disorder": 1,
    "Spherocytosis|ANK1-related_disorder|not_provided|Hereditary_spherocytosis_type_1": 1,
    "ANK1-related_disorder|not_provided|Hereditary_spherocytosis_type_1|Spherocytosis": 1,
    "ANK1-related_disorder|Hereditary_spherocytosis_type_1|Spherocytosis": 1,
    "not_specified|not_provided|Spherocytosis|Hereditary_spherocytosis_type_1": 1,
    "SPHEROCYTOSIS|_TYPE_1|_AUTOSOMAL_RECESSIVE": 2,
    "not_provided|Spherocytosis|Hereditary_spherocytosis_type_1|ANK1-related_disorder": 1,
    "Hereditary_spherocytosis_type_1|not_specified|not_provided|Spherocytosis": 1,
    "not_specified|SPHEROCYTOSIS|_TYPE_1|_AUTOSOMAL_RECESSIVE|Hereditary_spherocytosis_type_1|not_provided": 1,
    "not_provided|SPHEROCYTOSIS|_TYPE_1|_AUTOSOMAL_RECESSIVE": 1,
    "Inborn_genetic_diseases|KAT6A-related_disorder|not_provided": 5,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|KAT6A-related_disorder": 9,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 104,
    "not_provided|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|KAT6A-related_disorder": 1,
    "KAT6A-related_disorder": 16,
    "not_provided|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 13,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_provided": 24,
    "KAT6A-related_disorder|Inborn_genetic_diseases|not_provided": 9,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Inborn_genetic_diseases": 3,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|KAT6A-related_disorder|Inborn_genetic_diseases": 4,
    "not_provided|Inborn_genetic_diseases|KAT6A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 3,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "KAT6A-related_disorder|not_provided": 8,
    "KAT6A-related_disorder|not_provided|Inborn_genetic_diseases": 4,
    "KAT6A-related_disorder|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|See_cases|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_provided": 1,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Syndromic_intellectual_disability": 1,
    "KAT6A-related_neurodevelopmental_disorder_with_multiple_anomalies|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_provided": 5,
    "not_provided|Craniosynostosis_syndrome|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 1,
    "KAT6A-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 1,
    "Intellectual_disability|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_provided": 1,
    "KAT6A-related_disorder|not_specified|not_provided": 2,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|KAT6A-related_disorder": 1,
    "not_provided|History_of_neurodevelopmental_disorder": 7,
    "Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Syndromic_intellectual_disability|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 1,
    "not_provided|KAT6A-related_disorder|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome": 3,
    "Developmental_delay|Borderline_microcephaly|Absent_or_delayed_speech_development|not_provided": 1,
    "Global_developmental_delay|Neurodevelopmental_disorder": 1,
    "not_provided|Vein_of_Galen_aneurysmal_malformation": 1,
    "Inborn_genetic_diseases|KAT6A-related_disorder|not_provided|Intellectual_disability": 1,
    "not_provided|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|Inborn_genetic_diseases": 1,
    "KAT6A-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_intellectual_disability-craniofacial_anomalies-cardiac_defects_syndrome|not_provided": 1,
    "KAT6A-related_neurodevelopmental_disorder_with_multiple_anomalies": 1,
    "PLAT-related_disorder|not_provided": 1,
    "Pulmonary_embolism|Deep_venous_thrombosis": 1,
    "IKBKB-related_disorder": 10,
    "IKBKB-related_disorder|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 621,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|Inborn_genetic_diseases": 9,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_specified": 3,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_provided": 8,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|Immunodeficiency_15a": 6,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 16,
    "Immunodeficiency_15a|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 4,
    "not_provided|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 9,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_IKK2_deficiency|Immunodeficiency_15a": 1,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|IKBKB-related_disorder": 2,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|Aganglionic_megacolon": 1,
    "IKBKB-related_disorder|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 5,
    "not_provided|IKBKB-related_disorder|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 1,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|Immunodeficiency_15a|Inborn_genetic_diseases": 1,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Immunodeficiency_15a|Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 1,
    "Immunodeficiency_15a": 1,
    "Inborn_genetic_diseases|IKBKB-related_disorder|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 1,
    "Immunodeficiency_15a|Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_IKK2_deficiency|not_specified|not_provided": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Severe_combined_immunodeficiency_due_to_IKK2_deficiency": 1,
    "Idiopathic_basal_ganglia_calcification_1": 77,
    "not_provided|Idiopathic_basal_ganglia_calcification_1": 25,
    "Idiopathic_basal_ganglia_calcification_1|not_provided": 16,
    "Idiopathic_basal_ganglia_calcification_1|Inborn_genetic_diseases": 2,
    "not_provided|Idiopathic_basal_ganglia_calcification_1|Inborn_genetic_diseases": 3,
    "Idiopathic_basal_ganglia_calcification_1|SLC20A2-related_disorder": 1,
    "Idiopathic_basal_ganglia_calcification_1|not_specified|not_provided": 1,
    "SLC20A2-related_disorder|not_provided|Idiopathic_basal_ganglia_calcification_1": 3,
    "SLC20A2-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|SLC20A2-related_disorder|Idiopathic_basal_ganglia_calcification_1": 1,
    "SLC20A2-related_disorder": 5,
    "Idiopathic_basal_ganglia_calcification_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Idiopathic_basal_ganglia_calcification_1|SLC20A2-related_disorder": 4,
    "SLC20A2-related_disorder|not_provided": 2,
    "not_provided|SLC20A2-related_disorder": 3,
    "Idiopathic_basal_ganglia_calcification_1|not_provided|SLC20A2-related_disorder": 2,
    "not_specified|not_provided|Idiopathic_basal_ganglia_calcification_1": 2,
    "Inborn_genetic_diseases|Idiopathic_basal_ganglia_calcification_1|not_provided": 1,
    "Idiopathic_basal_ganglia_calcification_1|Inborn_genetic_diseases|not_provided": 2,
    "Idiopathic_basal_ganglia_calcification_1|SLC20A2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Idiopathic_basal_ganglia_calcification_1": 1,
    "SLC20A2-related_disorder|Idiopathic_basal_ganglia_calcification_1|not_provided": 1,
    "Torsion_dystonia_6": 123,
    "not_provided|Torsion_dystonia_6": 15,
    "Torsion_dystonia_6|not_provided": 9,
    "not_specified|Torsion_dystonia_6|Inborn_genetic_diseases|not_provided": 1,
    "Torsion_dystonia_6|Young-onset_Parkinson_disease": 1,
    "Torsion_dystonia_6|Inborn_genetic_diseases": 3,
    "not_provided|Torsion_dystonia_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Torsion_dystonia_6": 2,
    "Torsion_dystonia_6|not_specified|not_provided": 1,
    "not_specified|Torsion_dystonia_6|Multiple_mitochondrial_dysfunctions_syndrome_9b": 1,
    "THAP1-related_disorder|Torsion_dystonia_6": 2,
    "Torsion_dystonia_6|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Torsion_dystonia_6": 1,
    "not_specified|not_provided|Torsion_dystonia_6": 2,
    "Autosomal_dominant_sensory_ataxia_1": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_sensory_ataxia_1|Spastic_paraplegia_85|_autosomal_recessive|not_provided": 1,
    "not_specified|Autosomal_dominant_sensory_ataxia_1": 1,
    "Spastic_paraplegia_85|_autosomal_recessive|Autosomal_dominant_sensory_ataxia_1": 1,
    "not_provided|Autosomal_dominant_sensory_ataxia_1": 1,
    "Spastic_paraplegia_85|_autosomal_recessive": 3,
    "Spastic_paraplegia_85|_autosomal_recessive|Spastic_paraplegia|not_provided": 1,
    "not_provided|not_specified|Autosomal_dominant_sensory_ataxia_1": 1,
    "Autosomal_dominant_sensory_ataxia_1|Spastic_paraplegia_85|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia_85|_autosomal_recessive": 1,
    "Spastic_paraplegia_85|_autosomal_recessive|Autosomal_dominant_sensory_ataxia_1|Spastic_paraplegia": 1,
    "RNF170-related_disorder": 1,
    "not_provided|RNF170-related_disorder": 1,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_provided": 13,
    "not_provided|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 5,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 11,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 63,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 83,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Inborn_genetic_diseases|not_provided": 1,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 3,
    "POMK-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 2,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 1,
    "Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided": 6,
    "POMK-related_disorder|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 2,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_specified|not_provided": 4,
    "not_specified|POMK-related_disorder|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|POMK-related_disorder": 2,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_provided|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Inborn_genetic_diseases": 7,
    "POMK-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 1,
    "POMK-related_disorder": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided": 2,
    "not_specified|POMK-related_disorder|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_provided": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_provided|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 1,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided|POMK-related_disorder": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided": 1,
    "not_provided|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Inborn_genetic_diseases": 1,
    "Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency": 1,
    "not_specified|POMK-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided": 1,
    "not_provided|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_12|not_specified": 1,
    "Sanfilippo_syndrome": 38,
    "Mucopolysaccharidosis|_MPS-III-C": 163,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 14,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 471,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 385,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-C|Retinal_dystrophy|Retinitis_pigmentosa_73": 1,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Inborn_genetic_diseases": 6,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|not_specified": 5,
    "Retinal_dystrophy|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 3,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|HGSNAT-related_disorder|not_provided": 1,
    "Retinal_dystrophy|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 5,
    "not_provided|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 3,
    "Mucopolysaccharidosis|_MPS-III-C|not_specified|HGSNAT-related_disorder|not_provided|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Inborn_genetic_diseases": 8,
    "not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 5,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Retinal_dystrophy": 5,
    "Sanfilippo_syndrome|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Retinal_dystrophy|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-C|not_provided|Retinitis_pigmentosa_73": 2,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_provided|Retinal_dystrophy": 2,
    "HGSNAT-related_disorder|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_73": 1,
    "Intellectual_disability|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|not_provided|not_specified|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_73|Retinal_dystrophy|Retinitis_pigmentosa|Mucopolysaccharidosis|_MPS-III-C|not_provided": 1,
    "Retinitis_pigmentosa_73|not_provided|Mucopolysaccharidosis|_MPS-III-C": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-C|Sanfilippo_syndrome|Retinitis_pigmentosa_73": 1,
    "Retinitis_pigmentosa_73": 5,
    "HGSNAT-related_disorder": 4,
    "Mucopolysaccharidosis|_MPS-III-C|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_73|Sanfilippo_syndrome": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 2,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_provided": 5,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Sanfilippo_syndrome|Mucopolysaccharidosis|not_provided": 1,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Sanfilippo_syndrome|Retinal_dystrophy": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|HGSNAT-related_disorder": 2,
    "Retinal_dystrophy|Mucopolysaccharidosis|_MPS-III-C|HGSNAT-related_disorder|Retinitis_pigmentosa_73": 1,
    "HGSNAT-related_disorder|Mucopolysaccharidosis|_MPS-III-C|Inborn_genetic_diseases|Retinitis_pigmentosa_73": 1,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_specified|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Sanfilippo_syndrome": 1,
    "not_specified|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 1,
    "Mucopolysaccharidosis": 2,
    "not_specified|Mucopolysaccharidosis|_MPS-III-C|HGSNAT-related_disorder|Retinitis_pigmentosa_73": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 6,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_specified": 2,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Sanfilippo_syndrome|Retinal_dystrophy|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|not_provided": 4,
    "Retinal_dystrophy|Mucopolysaccharidosis|_MPS-III-C|not_specified|Retinitis_pigmentosa_73|HGSNAT-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Synovial_plica_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Sanfilippo_syndrome|Retinitis_pigmentosa_73": 1,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|HGSNAT-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Sanfilippo_syndrome|Retinal_dystrophy|Mucopolysaccharidosis|not_provided": 1,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Retinal_dystrophy": 2,
    "Sanfilippo_syndrome|not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|HGSNAT-related_disorder|Retinitis_pigmentosa_73": 2,
    "Mucopolysaccharidosis|_MPS-III-C|Inborn_genetic_diseases|Retinitis_pigmentosa_73": 2,
    "Inborn_genetic_diseases|Sanfilippo_syndrome|not_provided|not_specified|Retinitis_pigmentosa_73|Retinal_dystrophy|Mucopolysaccharidosis|_MPS-III-C": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-C|not_specified|Retinal_dystrophy|not_provided|HGSNAT-related_disorder|Retinitis_pigmentosa_73": 1,
    "Retinal_dystrophy|not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Sanfilippo_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Sanfilippo_syndrome": 1,
    "not_provided|Sanfilippo_syndrome|Retinal_dystrophy|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_specified|not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "HGSNAT-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|not_provided": 1,
    "Sanfilippo_syndrome|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Sanfilippo_syndrome|Retinitis_pigmentosa_73|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Retinal_dystrophy|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|Sanfilippo_syndrome|Retinal_dystrophy|not_provided": 2,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|not_specified|not_provided|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|not_specified": 2,
    "HGSNAT-related_disorder|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C": 1,
    "Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73|not_specified|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Mucopolysaccharidosis|_MPS-III-C|Retinitis_pigmentosa_73": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-C|not_specified|Retinitis_pigmentosa_73": 1,
    "Inborn_genetic_diseases|not_specified|Mucopolysaccharidosis|_MPS-III-C|not_provided|HGSNAT-related_disorder|Retinitis_pigmentosa_73": 1,
    "Retinal_dystrophy|Mucopolysaccharidosis|_MPS-III-C|not_provided|Retinitis_pigmentosa_73": 1,
    "Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|not_provided|not_specified": 1,
    "HGSNAT-related_disorder|Retinitis_pigmentosa_73|Mucopolysaccharidosis|_MPS-III-C|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Intellectual_disability|HGSNAT-related_disorder|Retinal_dystrophy|not_specified|Mucopolysaccharidosis|_MPS-III-C|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_73": 1,
    "Mucopolysaccharidosis|_MPS-III-C|not_provided": 6,
    "not_provided|Mucopolysaccharidosis|_MPS-III-C": 1,
    "Knobloch_syndrome_1": 11,
    "SPIDR-related_disorder": 1,
    "Ovarian_dysgenesis_9": 5,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 1913,
    "not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 173,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_provided": 39,
    "not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 37,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified": 240,
    "not_specified|PRKDC-related_disorder|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 2,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified|not_provided": 18,
    "not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified": 9,
    "not_specified|PRKDC-related_disorder": 6,
    "not_specified|not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 7,
    "PRKDC-related_disorder|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 8,
    "PRKDC-related_disorder": 5,
    "not_provided|not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 3,
    "not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|Malignant_tumor_of_breast|not_specified": 1,
    "Immunodeficiency_26_without_neurologic_abnormalities|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_provided": 5,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_provided|PRKDC-related_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified|PRKDC-related_disorder": 1,
    "PRKDC-related_disorder|not_specified": 2,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|PRKDC-related_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|PRKDC-related_disorder|not_provided": 2,
    "PRKDC-related_disorder|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified": 2,
    "PRKDC-related_disorder|not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_provided|not_specified": 3,
    "PRKDC-related_disorder|not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 1,
    "See_cases|not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|PRKDC-related_disorder|not_specified": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|not_specified|PRKDC-related_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|PRKDC-related_disorder|not_specified": 8,
    "not_provided|not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|PRKDC-related_disorder": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency|PRKDC-related_disorder|not_provided": 1,
    "PRKDC-related_disorder|not_specified|Severe_combined_immunodeficiency_due_to_DNA-PKcs_deficiency": 1,
    "Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency": 67,
    "Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|not_provided": 26,
    "not_specified|not_provided|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency": 6,
    "not_provided|MCM4-related_disorder": 3,
    "not_provided|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency": 15,
    "not_provided|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|not_specified": 1,
    "MCM4-related_disorder|not_provided|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency": 2,
    "Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|not_specified|not_provided": 5,
    "Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|MCM4-related_disorder|not_provided": 2,
    "not_provided|not_specified|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency": 1,
    "MCM4-related_disorder|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|not_provided": 1,
    "MCM4-related_disorder|not_provided": 2,
    "not_provided|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|MCM4-related_disorder": 2,
    "not_specified|Microcephaly|not_provided": 1,
    "not_provided|MCM4-related_disorder|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency": 1,
    "not_specified|Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|not_provided": 1,
    "Primary_immunodeficiency_with_natural-killer_cell_deficiency_and_adrenal_insufficiency|not_provided|MCM4-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_53": 4,
    "not_provided|not_specified|Piebaldism|SNAI2-related_disorder": 1,
    "not_specified|Piebaldism|SNAI2-related_disorder|not_provided": 1,
    "not_specified|Piebaldism": 1,
    "not_provided|SNAI2-related_disorder": 3,
    "not_provided|Piebaldism": 3,
    "Piebaldism|SNAI2-related_disorder": 1,
    "SNTG1-related_disorder|not_provided": 1,
    "SNTG1-related_disorder": 16,
    "PXDNL-related_disorder": 26,
    "not_provided|PXDNL-related_disorder": 5,
    "PXDNL-related_disorder|not_provided": 12,
    "not_specified|PXDNL-related_disorder|not_provided": 2,
    "not_specified|PXDNL-related_disorder": 2,
    "not_provided|not_specified|PXDNL-related_disorder": 1,
    "not_provided|PXDNL-related_disorder|not_specified": 1,
    "Vesicoureteral_reflux_3": 46,
    "SOX17-related_disorder": 4,
    "Vesicoureteral_reflux_3|not_provided": 6,
    "Inborn_genetic_diseases|Vesicoureteral_reflux_3": 4,
    "Sox17-_related_disorders": 1,
    "not_provided|SOX17-related_disorder": 6,
    "not_provided|Vesicoureteral_reflux_3": 4,
    "Vesicoureteral_reflux_3|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|SOX17-related_disorder|Vesicoureteral_reflux_3": 1,
    "not_provided|SOX17-related_pulmonary_arterial_hypertension": 1,
    "Vesicoureteral_reflux_3|Inborn_genetic_diseases": 3,
    "Vesicoureteral_reflux_3|not_provided|SOX17-related_disorder": 1,
    "SOX17-related_disorder|Inborn_genetic_diseases": 1,
    "SOX17-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "SOX17-related_disorder|not_provided|Chronic_kidney_disease": 1,
    "Inborn_genetic_diseases|not_provided|Vesicoureteral_reflux_3": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_1": 4,
    "RP1-related_disorder|not_provided": 4,
    "not_provided|Retinitis_pigmentosa_1": 16,
    "RP1-related_disorder|not_specified|not_provided|Retinal_dystrophy": 1,
    "not_provided|RP1-related_disorder": 7,
    "Inborn_genetic_diseases|RP1-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_1|Autosomal_recessive_retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "RP1-related_disorder": 4,
    "RP1-related_retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_1|RP1-related_recessive_retinopathy|not_provided": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa|Retinitis_pigmentosa_1": 1,
    "RP1-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_1": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_1|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_1|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_1|Retinal_dystrophy": 2,
    "not_provided|Retinitis_pigmentosa_1|Retinal_dystrophy": 4,
    "Retinitis_pigmentosa_1|not_provided": 9,
    "RP1-related_retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_1|Retinal_dystrophy|not_provided": 4,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_1": 2,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_1|Retinal_dystrophy": 1,
    "not_provided|RP1-related_recessive_retinopathy": 1,
    "RP1-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_1": 1,
    "Retinitis_pigmentosa_1|Retinitis_pigmentosa": 3,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_1": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_1|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_1": 1,
    "RP1-related_disorder|Cone-rod_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_1": 2,
    "RP1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_1|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_1": 3,
    "Retinitis_pigmentosa_1|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Hypertriglyceridemia_1|Retinitis_pigmentosa_1": 1,
    "Retinitis_pigmentosa|not_specified|not_provided|Retinitis_pigmentosa_1": 1,
    "Retinitis_pigmentosa|RP1-related_disorder|not_provided": 2,
    "not_specified|Retinitis_pigmentosa_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_1": 2,
    "not_provided|RP1-related_disorder|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_1|not_provided|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_1|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|RP1-related_disorder|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_1|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_1|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|Retinitis_pigmentosa_1": 2,
    "RP1-related_disorder|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_1": 1,
    "Retinitis_pigmentosa_1|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_1|not_provided": 3,
    "not_provided|Leber_optic_atrophy": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|not_provided|RP1-related_disorder": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_1": 2,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_1|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_1": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_1|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinal_pigment_epithelial_atrophy|Visual_impairment|Optic_atrophy|not_provided": 1,
    "not_specified|Retinitis_pigmentosa|RP1-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_1|RP1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_1": 1,
    "LYN-related_disorder|not_provided": 4,
    "Autoinflammatory_disease|_systemic|_with_vasculitis": 2,
    "Autoinflammatory_disease|_systemic|_with_vasculitis|LYN_kinase_associated_vasculopathy_and_liver_fibrosis_syndrome": 3,
    "not_specified|not_provided|Lynch_syndrome": 1,
    "RPS20-related_disorder": 2,
    "not_specified|not_provided|Familial_colorectal_cancer_type_X": 1,
    "not_specified|not_provided|RPS20-related_disorder": 1,
    "not_specified|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "Familial_colorectal_cancer_type_X|not_provided|not_specified": 1,
    "not_specified|RPS20-related_disorder": 2,
    "not_provided|Familial_colorectal_cancer_type_X": 2,
    "Diamond-Blackfan_anemia|Familial_colorectal_cancer_type_X": 1,
    "not_specified|not_provided|Familial_colorectal_cancer_type_X|Diamond-Blackfan_anemia": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_specified": 2,
    "not_specified|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|Hereditary_nonpolyposis_colon_cancer|not_specified": 1,
    "not_specified|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Diamond-Blackfan_anemia": 1,
    "not_provided|not_specified|Familial_colorectal_cancer_type_X": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Lynch_syndrome": 1,
    "Oocyte/zygote/embryo_maturation_arrest_20": 11,
    "Silver-russell_syndrome_4|Silver-Russell_syndrome_1": 2,
    "PLAG1-related_disorder": 3,
    "PLAG1-related_disorder|Inborn_genetic_diseases": 2,
    "Silver-russell_syndrome_4": 4,
    "not_provided|Silver-russell_syndrome_4": 1,
    "Russell-Silver_syndrome": 1,
    "Chondrodysplasia_with_joint_dislocations|_gPAPP_type": 137,
    "Chondrodysplasia": 14,
    "not_provided|Chondrodysplasia_with_joint_dislocations|_gPAPP_type": 20,
    "Chondrodysplasia_with_joint_dislocations|_gPAPP_type|not_provided": 4,
    "not_specified|Chondrodysplasia_with_joint_dislocations|_gPAPP_type": 1,
    "not_provided|BPNT2-related_disorder": 1,
    "not_provided|BPNT2-related_disorder|Chondrodysplasia_with_joint_dislocations|_gPAPP_type": 2,
    "not_provided|not_specified|Chondrodysplasia_with_joint_dislocations|_gPAPP_type": 3,
    "BPNT2-related_disorder": 3,
    "CYP7A1-related_disorder": 18,
    "not_provided|CYP7A1-related_disorder": 8,
    "CYP7A1-related_disorder|not_provided": 8,
    "CYP7A1-related_disorder|not_specified|not_provided": 1,
    "not_specified|CYP7A1-related_disorder": 1,
    "not_specified|CYP7A1-related_disorder|not_provided": 1,
    "CYP7A1-related_disorder|not_specified": 1,
    "Iron-refractory_iron_deficiency_anemia": 19,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_3": 10,
    "Inborn_genetic_diseases|not_specified|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_3": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_3|not_provided": 2,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_3": 1,
    "CHARGE_syndrome|not_provided|Hypogonadism_with_anosmia": 2,
    "CHARGE_syndrome|Hypogonadism_with_anosmia": 5,
    "not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 5,
    "Hypogonadism_with_anosmia|CHARGE_syndrome": 10,
    "not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 19,
    "CHARGE_syndrome|Inborn_genetic_diseases": 51,
    "CHARGE_syndrome|Inborn_genetic_diseases|CHD7-related_disorder|not_provided": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 145,
    "CHARGE_syndrome|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_specified": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_provided|CHARGE_syndrome": 2,
    "CHARGE_syndrome|CHD7-related_disorder|not_provided": 5,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 25,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|CHARGE_syndrome|Inborn_genetic_diseases|CHD7-related_disorder": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 105,
    "CHD7-related_disorder": 62,
    "Inborn_genetic_diseases|not_specified|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 15,
    "CHARGE_syndrome|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 7,
    "Inborn_genetic_diseases|not_provided|CHARGE_syndrome": 25,
    "not_provided|CHD7-related_disorder": 5,
    "not_provided|CHARGE_syndrome|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 2,
    "Inborn_genetic_diseases|CHARGE_syndrome": 77,
    "Inborn_genetic_diseases|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 9,
    "Inborn_genetic_diseases|CHARGE_syndrome|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 12,
    "not_provided|not_specified|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases": 16,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|CHARGE_syndrome|not_provided|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|See_cases": 2,
    "CHARGE_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "not_specified|CHARGE_syndrome|Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 2,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_specified|not_provided|CHARGE_syndrome": 2,
    "CHD7-related_disorder|CHARGE_syndrome": 18,
    "Inborn_genetic_diseases|CHARGE_syndrome|CHD7-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 2,
    "CHARGE_syndrome|CHD7-related_disorder|Inborn_genetic_diseases": 4,
    "not_provided|See_cases|CHARGE_syndrome": 1,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Congenital_heart_disease|Inborn_genetic_diseases": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|Inborn_genetic_diseases": 6,
    "CHD7-related_disorder|not_provided": 4,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 40,
    "Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 14,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 3,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 8,
    "Amenorrhea|CHARGE_syndrome": 1,
    "CHD7-related_disorder|not_provided|CHARGE_syndrome": 10,
    "CHARGE_syndrome|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 6,
    "Inborn_genetic_diseases|CHARGE_syndrome|not_provided": 3,
    "not_provided|CHARGE_syndrome|Inborn_genetic_diseases": 11,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|Hypogonadism_with_anosmia": 1,
    "not_provided|CHARGE_syndrome|CHD7-related_disorder|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 2,
    "Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 7,
    "CHARGE_syndrome|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|CHARGE_syndrome": 12,
    "not_provided|Inborn_genetic_diseases|CHARGE_syndrome|CHD7-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 3,
    "not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder|CHARGE_syndrome": 2,
    "not_provided|CHD7-related_disorder|CHARGE_syndrome": 4,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases|not_provided": 8,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases": 6,
    "CHARGE_syndrome|CHD7-related_disorder": 16,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_specified": 5,
    "Inborn_genetic_diseases|not_specified|CHD7-related_disorder|CHARGE_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|CHARGE_syndrome|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder|Amenorrhea": 1,
    "CHARGE_syndrome|not_provided|CHD7-related_disorder": 1,
    "not_provided|CHARGE_syndrome|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "not_specified|CHD7-related_disorder|Inborn_genetic_diseases|CHARGE_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|CHARGE_syndrome": 9,
    "Hearing_impairment|Pulmonary_artery_atresia|Retinal_coloboma|Chorioretinal_coloboma|CHARGE_syndrome": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 3,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Premature_ovarian_failure|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder|CHARGE_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|not_specified": 1,
    "not_specified|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 7,
    "Scoliosis|_isolated|_susceptibility_to|_3": 2,
    "not_provided|CHARGE_syndrome|CHD7-related_disorder": 5,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|CHARGE_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 4,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 3,
    "Inborn_genetic_diseases|CHARGE_syndrome|not_provided|CHD7-related_disorder": 1,
    "CHARGE_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "not_specified|Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "Congenital_heart_disease_(variable)": 4,
    "Inborn_genetic_diseases|CHARGE_syndrome|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hypogonadism_with_anosmia|CHARGE_syndrome": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|CHARGE_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 5,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder": 6,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|not_provided": 3,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Amenorrhea|CHD7-related_disorder|Inborn_genetic_diseases": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|CHARGE_syndrome|CHD7-related_disorder|Inborn_genetic_diseases": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_provided|CHARGE_syndrome": 6,
    "Inborn_genetic_diseases|CHD7-related_disorder|Neurodevelopmental_disorder": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 1,
    "CHARGE_syndrome|not_provided|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 2,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 4,
    "CHARGE_syndrome|not_specified|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_specified|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 3,
    "HYPOGONADOTROPIC_HYPOGONADISM_5_WITHOUT_ANOSMIA|CHARGE_syndrome": 1,
    "Childhood_onset_hearing_loss|Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "CHD7-related_disorder|not_provided|not_specified|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 4,
    "Inborn_genetic_diseases|not_provided|not_specified|CHARGE_syndrome": 4,
    "Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 6,
    "not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "not_provided|CHARGE_syndrome|Intellectual_disability": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_specified|CHD7-related_disorder|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|CHARGE_syndrome|not_specified|not_provided|CHD7-related_disorder": 1,
    "CHD7-related_disorder|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "Atrial_septal_defect|Pyloric_stenosis|Abnormal_facial_shape|Choanal_atresia": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder": 1,
    "Inborn_genetic_diseases|CHARGE_syndrome|CHD7-related_disorder": 2,
    "not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|See_cases": 1,
    "VATER_association|CHARGE_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hypogonadism_with_anosmia|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 2,
    "Bilateral_hearing_loss|_bilateral_enlarged_vestibular_aqueduct_(EVA)": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_specified|not_provided": 1,
    "CHARGE_syndrome|not_specified|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "CHD7-related_disorder|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 2,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 4,
    "CHD7_disorder": 1,
    "Pure_gonadal_dysgenesis_46|XY": 3,
    "Primary_dilated_cardiomyopathy|CHARGE_syndrome|not_provided": 1,
    "not_provided|not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|Inborn_genetic_diseases": 4,
    "not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 1,
    "not_specified|CHARGE_syndrome|Inborn_genetic_diseases": 2,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|CHARGE_syndrome": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Hypogonadism_with_anosmia": 1,
    "not_specified|CHARGE_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "CHD7-related_disorder|not_provided|Inborn_genetic_diseases|CHARGE_syndrome": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|not_provided|CHD7-related_disorder": 1,
    "CHARGE_syndrome|CHD7-related_disorder|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder|Inborn_genetic_diseases": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|not_specified": 1,
    "CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "Inborn_genetic_diseases|not_specified|CHARGE_syndrome": 2,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|CHARGE_syndrome": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|not_provided|Bilateral_hearing_loss|_bilateral_enlarged_vestibular_aqueduct_(EVA)": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 2,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|3MC_syndrome": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases|not_specified|not_provided|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|CHARGE_syndrome|CHD7-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|Inborn_genetic_diseases|CHARGE_syndrome": 1,
    "CHD7-related_disorder|not_specified|CHARGE_syndrome": 4,
    "Intellectual_disability|not_provided|not_specified|CHARGE_syndrome": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Amenorrhea|Inborn_genetic_diseases|not_provided": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|Intellectual_disability": 1,
    "Iris_coloboma": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|Familial_atrioventricular_septal_defect|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHD7-related_disorder|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_specified|not_provided": 1,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Cystic_fibrosis": 1,
    "Neurodevelopmental_disorder|not_provided|CHARGE_syndrome|CHD7-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|Male_infertility_with_spermatogenesis_disorder|not_provided|CHD7-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|Hearing_impairment": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_specified|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder|not_provided": 1,
    "not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Hearing_impairment|Inborn_genetic_diseases": 1,
    "not_specified|CHD7-related_disorder|CHARGE_syndrome": 1,
    "not_specified|not_provided|Hearing_impairment|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|CHD7-related_disorder": 1,
    "not_provided|CHD7-related_disorder|Inborn_genetic_diseases": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "Inborn_genetic_diseases|not_provided|CHD7-related_disorder|CHARGE_syndrome": 1,
    "CHD7-related_disorder|CHARGE_syndrome|not_provided": 3,
    "CHARGE_syndrome|CHD7-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CHD7-related_disorder|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "CHARGE_syndrome|CHD7-related_disorder|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 1,
    "Myopia|Dolichocephaly|Progressive_hearing_impairment|Scoliosis|Hypothyroidism|Poor_coordination": 1,
    "CHD7-related_disorder|not_provided|CHARGE_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|CHD7-related_disorder|not_provided": 1,
    "not_provided|CHARGE_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|CHARGE_syndrome|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|CHD7-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|CHARGE_syndrome|not_specified": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHD7-related_disorder|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|CHD7-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases|CHARGE_syndrome": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "not_specified|CHARGE_syndrome|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "not_specified|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome|CHD7-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|CHD7-related_disorder|not_specified|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|Amenorrhea": 1,
    "Inborn_genetic_diseases|not_provided|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHARGE_syndrome": 1,
    "Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided|CHD7-related_disorder": 1,
    "CHD7-related_disorder|Inborn_genetic_diseases|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|CHD7-related_disorder": 1,
    "CHD7-related_disorder|CHARGE_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CHARGE_syndrome|not_specified|CHD7-related_disorder": 1,
    "Cleft_palate|CHD7-related_disorder|Inborn_genetic_diseases|not_provided|CHARGE_syndrome": 1,
    "CHARGE_syndrome|CHD7-related_disorder|Intellectual_disability": 2,
    "Inborn_genetic_diseases|not_provided|CHARGE_syndrome|CHD7-related_disorder": 1,
    "CHARGE_syndrome|not_provided|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CHARGE_syndrome|Inborn_genetic_diseases": 1,
    "Hearing_impairment|not_provided|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|CHARGE_syndrome|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_specified": 1,
    "CHARGE_syndrome|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia|not_provided": 1,
    "CHD7-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|CHARGE_syndrome": 1,
    "not_specified|not_provided|CHARGE_syndrome|Inborn_genetic_diseases|CHD7-related_disorder|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|not_provided|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_5_with_or_without_anosmia": 1,
    "CHARGE_syndrome|Intellectual_disability": 1,
    "not_provided|CHD7-related_disorder|Inborn_genetic_diseases|CHARGE_syndrome": 1,
    "not_provided|Hypogonadism_with_anosmia|CHARGE_syndrome": 2,
    "Thoracic_aortic_aneurysm_or_dissection|Facial_dysmorphism-lens_dislocation-anterior_segment_abnormalities-spontaneous_filtering_blebs_syndrome": 1,
    "not_provided|Facial_dysmorphism-lens_dislocation-anterior_segment_abnormalities-spontaneous_filtering_blebs_syndrome": 11,
    "Facial_dysmorphism-lens_dislocation-anterior_segment_abnormalities-spontaneous_filtering_blebs_syndrome": 19,
    "ASPH-related_disorder": 7,
    "ASPH-related_disorder|not_provided": 2,
    "not_provided|ASPH-related_disorder": 5,
    "Facial_dysmorphism-lens_dislocation-anterior_segment_abnormalities-spontaneous_filtering_blebs_syndrome|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|ASPH-related_disorder": 1,
    "not_provided|Exercise-induced_malignant_hyperthermia": 1,
    "Exercise-induced_malignant_hyperthermia": 1,
    "Malignant_hyperthermia_of_anesthesia|Inborn_genetic_diseases": 1,
    "Familial_isolated_deficiency_of_vitamin_E": 94,
    "not_provided|Familial_isolated_deficiency_of_vitamin_E": 25,
    "Familial_isolated_deficiency_of_vitamin_E|not_provided": 18,
    "Familial_isolated_deficiency_of_vitamin_E|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|Familial_isolated_deficiency_of_vitamin_E|not_provided": 2,
    "not_provided|Familial_isolated_deficiency_of_vitamin_E|ATAXIA|_FRIEDREICH-LIKE|_WITH_ISOLATED_VITAMIN_E_DEFICIENCY": 2,
    "Familial_isolated_deficiency_of_vitamin_E|not_provided|not_specified": 1,
    "TTPA-related_disorder|not_specified|not_provided|Familial_isolated_deficiency_of_vitamin_E|ATAXIA|_FRIEDREICH-LIKE|_WITH_ISOLATED_VITAMIN_E_DEFICIENCY": 1,
    "not_provided|TTPA-related_disorder": 2,
    "Retinal_dystrophy|not_provided|Familial_isolated_deficiency_of_vitamin_E|ATAXIA|_FRIEDREICH-LIKE|_WITH_ISOLATED_VITAMIN_E_DEFICIENCY": 1,
    "Familial_isolated_deficiency_of_vitamin_E|not_provided|ATAXIA|_FRIEDREICH-LIKE|_WITH_ISOLATED_VITAMIN_E_DEFICIENCY": 1,
    "not_provided|Familial_isolated_deficiency_of_vitamin_E|not_specified": 2,
    "Familial_isolated_deficiency_of_vitamin_E|not_provided|Retinal_dystrophy|not_specified": 1,
    "TTPA-related_disorder": 1,
    "TTPA-related_disorder|Retinal_dystrophy|not_provided|Familial_isolated_deficiency_of_vitamin_E|ATAXIA|_FRIEDREICH-LIKE|_WITH_ISOLATED_VITAMIN_E_DEFICIENCY": 1,
    "not_provided|not_specified|Familial_isolated_deficiency_of_vitamin_E": 3,
    "Familial_isolated_deficiency_of_vitamin_E|ATAXIA_WITH_ISOLATED_VITAMIN_E_DEFICIENCY_AND_RETINITIS_PIGMENTOSA": 1,
    "Familial_isolated_deficiency_of_vitamin_E|Inborn_genetic_diseases": 1,
    "not_provided|Familial_isolated_deficiency_of_vitamin_E|Inborn_genetic_diseases": 2,
    "not_provided|Familial_isolated_deficiency_of_vitamin_E|TTPA-related_disorder": 2,
    "TTPA-related_disorder|not_provided": 1,
    "Familial_isolated_deficiency_of_vitamin_E|not_specified": 1,
    "Familial_isolated_deficiency_of_vitamin_E|not_specified|not_provided": 1,
    "not_specified|Familial_isolated_deficiency_of_vitamin_E|not_provided": 1,
    "CYP7B1-related_disorder": 5,
    "Hereditary_spastic_paraplegia_5A|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_5A": 2,
    "CYP7B1-related_disorder|not_provided|Spastic_paraplegia": 1,
    "Congenital_bile_acid_synthesis_defect_3|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "CYP7B1-related_disorder|Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_5A|Congenital_bile_acid_synthesis_defect_3|not_specified": 1,
    "Spastic_Paraplegia|_Recessive|Congenital_bile_acid_synthesis_defect|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_5A|Spastic_paraplegia|CYP7B1-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Congenital_bile_acid_synthesis_defect|Spastic_Paraplegia|_Recessive": 2,
    "Hereditary_spastic_paraplegia_5A|Congenital_bile_acid_synthesis_defect_3|Spastic_paraplegia": 2,
    "Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A": 3,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_5A": 1,
    "Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A": 3,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 10,
    "Spastic_paraplegia|not_specified|Inborn_genetic_diseases": 3,
    "Spastic_paraplegia|CYP7B1-related_disorder": 5,
    "Inborn_genetic_diseases|CYP7B1-related_disorder|Spastic_paraplegia": 1,
    "Congenital_bile_acid_synthesis_defect_3": 3,
    "Hereditary_spastic_paraplegia_5A|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_5A|not_provided": 2,
    "CYP7B1-related_disorder|Spastic_paraplegia|not_provided": 3,
    "CYP7B1-related_disorder|Spastic_paraplegia": 10,
    "not_specified|Hereditary_spastic_paraplegia|Spastic_paraplegia": 2,
    "not_provided|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_5A|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|CYP7B1-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided": 1,
    "CYP7B1-related_disorder|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "Hereditary_spastic_paraplegia_5A|not_provided": 2,
    "Hereditary_spastic_paraplegia_5A|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "CYP7B1-related_disorder|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "CYP7B1-related_disorder|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_5A|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_5A|Congenital_bile_acid_synthesis_defect_3|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_5A|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A|not_provided": 1,
    "CYP7B1-related_disorder|Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3|not_provided|Hereditary_spastic_paraplegia_5A": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "CYP7B1-related_disorder|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|not_provided|Congenital_bile_acid_synthesis_defect_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_5A|Congenital_bile_acid_synthesis_defect_3|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_5A|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|not_specified|Congenital_bile_acid_synthesis_defect|Spastic_Paraplegia|_Recessive": 1,
    "CYP7B1-related_disorder|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_5A|Congenital_bile_acid_synthesis_defect_3": 1,
    "not_specified|Hereditary_spastic_paraplegia_5A": 2,
    "CYP7B1-related_disorder|not_provided|Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "Congenital_bile_acid_synthesis_defect|Spastic_Paraplegia|_Recessive|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|not_specified": 2,
    "Spastic_paraplegia|Congenital_bile_acid_synthesis_defect_3|not_provided|not_specified|Hereditary_spastic_paraplegia_5A": 1,
    "CYP7B1-related_disorder|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "not_specified|CYP7B1-related_disorder|Spastic_paraplegia": 1,
    "CYP7B1-related_disorder|not_provided": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_5A|not_provided": 1,
    "CYP7B1-related_disorder|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "CYP7B1-related_disorder|not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_5A": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_5A|Hereditary_spastic_paraplegia": 1,
    "CYP7B1-related_disorder|Congenital_bile_acid_synthesis_defect_3|Hereditary_spastic_paraplegia_5A|not_provided|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_5A|not_provided|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_3": 1,
    "TRIM55-related_disorder": 15,
    "not_specified|TRIM55-related_disorder": 1,
    "not_provided|TRIM55-related_disorder": 1,
    "CRH-related_disorder|not_specified|not_provided": 1,
    "CRH-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Joubert_syndrome_21": 834,
    "Joubert_syndrome_21|not_provided": 34,
    "Joubert_syndrome_21|CSPP1-related_disorder|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_21|not_specified|not_provided|CSPP1-related_disorder": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_21": 52,
    "Joubert_syndrome_21|not_provided|Inborn_genetic_diseases": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_21": 1,
    "Joubert_syndrome_21|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_21": 2,
    "not_specified|Joubert_syndrome_21|not_provided": 2,
    "Joubert_syndrome_21|CSPP1-related_disorder": 7,
    "not_provided|Joubert_syndrome_21": 28,
    "Joubert_syndrome_21|Inborn_genetic_diseases": 31,
    "not_specified|not_provided|Joubert_syndrome_21": 3,
    "Optic_atrophy|Joubert_syndrome_21|not_provided": 1,
    "not_provided|Joubert_syndrome_21|CSPP1-related_disorder": 1,
    "CSPP1-related_disorder|Joubert_syndrome_21|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_21|not_provided": 5,
    "Joubert_syndrome_21|Inborn_genetic_diseases|not_provided": 6,
    "CSPP1-related_disorder|Joubert_syndrome_21": 8,
    "CSPP1-related_disorder": 5,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_21": 5,
    "Dandy-Walker_malformation": 1,
    "Retinal_dystrophy|Joubert_syndrome_21": 1,
    "Joubert_syndrome_21|not_provided|CSPP1-related_disorder": 3,
    "Joubert_syndrome_21|Retinal_dystrophy": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_21|Retinal_dystrophy|not_provided": 1,
    "Joubert_syndrome_21|not_specified|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_21|not_provided|not_specified": 4,
    "not_specified|Joubert_syndrome_21": 3,
    "Joubert_syndrome_21|not_specified": 2,
    "Microcephaly|CSPP1-related_disorder|Joubert_syndrome_21": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Joubert_syndrome_21": 1,
    "CSPP1-related_disorder|Joubert_syndrome_21|not_provided": 3,
    "Joubert_syndrome_21|Inborn_genetic_diseases|CSPP1-related_disorder": 1,
    "not_provided|Joubert_syndrome_21|Inborn_genetic_diseases": 1,
    "CSPP1-related_disorder|Joubert_syndrome_21|not_provided|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_21|Retinal_dystrophy|not_provided": 1,
    "not_provided|not_specified|Joubert_syndrome_21": 3,
    "Joubert_syndrome_21|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "CSPP1-related_disorder|Inborn_genetic_diseases|Joubert_syndrome_21": 1,
    "not_provided|not_specified|CSPP1-related_disorder|Joubert_syndrome_21": 1,
    "not_provided|CSPP1-related_disorder|Joubert_syndrome_21": 2,
    "not_specified|not_provided|CSPP1-related_disorder|Joubert_syndrome_21": 1,
    "ARFGEF1-related_disorder": 11,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures": 60,
    "Inborn_genetic_diseases|ARFGEF1-related_disorder": 1,
    "Global_developmental_delay|Seizure|Intellectual_disability|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures|not_provided|Delayed_speech_and_language_development|Atypical_behavior": 1,
    "Delayed_ability_to_walk": 1,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures|not_provided": 1,
    "Inborn_genetic_diseases|ARFGEF1-related_disorder|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "DEVELOPMENTAL_DELAY|_IMPAIRED_SPEECH|_BEHAVIORAL_ABNORMALITIES|_AND_SEIZURES": 1,
    "Delayed_speech_and_language_development|Atypical_behavior|Global_developmental_delay|Intellectual_disability|not_provided": 1,
    "ARFGEF1-related_disorder|Inborn_genetic_diseases": 1,
    "Delayed_speech_and_language_development|Atypical_behavior|Global_developmental_delay|Intellectual_disability": 4,
    "not_provided|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "ARFGEF1-related_disorder|not_provided": 1,
    "ARFGEF1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "DEVELOPMENTAL_DELAY|_IMPAIRED_SPEECH|_BEHAVIORAL_ABNORMALITIES|_AND_SEIZURES|Seizure": 1,
    "not_provided|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures|Intellectual_disability|Global_developmental_delay|Delayed_speech_and_language_development|Atypical_behavior": 1,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures|Delayed_speech_and_language_development|Atypical_behavior|Global_developmental_delay|Intellectual_disability": 1,
    "Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "ARFGEF1-related_disorder|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "Intellectual_disability|Focal-onset_seizure": 1,
    "DEVELOPMENTAL_DELAY|_IMPAIRED_SPEECH|_BEHAVIORAL_ABNORMALITIES|_AND_SEIZURES|Delayed_speech_and_language_development|Atypical_behavior|Global_developmental_delay|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Developmental_delay|_impaired_speech|_and_behavioral_abnormalities|_with_or_without_seizures": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_5": 4,
    "Familial_temporal_lobe_epilepsy_5": 33,
    "Febrile_seizures|_familial|_11": 69,
    "Febrile_seizures|_familial|_11|not_specified": 9,
    "not_specified|Febrile_seizures|_familial|_11|Familial_temporal_lobe_epilepsy_5": 2,
    "not_provided|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11": 2,
    "not_provided|not_specified|Febrile_seizures|_familial|_11": 1,
    "See_cases|Febrile_seizures|_familial|_11": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_2": 3,
    "not_specified|Febrile_seizures|_familial|_11": 6,
    "not_provided|Febrile_seizures|_familial|_11|not_specified": 3,
    "CPA6-related_disorder": 2,
    "Febrile_seizures|_familial|_11|not_provided|CPA6-related_disorder": 1,
    "Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11": 7,
    "Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|not_specified|not_provided": 2,
    "Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|not_provided": 4,
    "Febrile_seizures|_familial|_11|Epilepsy": 1,
    "Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|Intellectual_disability": 1,
    "Febrile_seizures|_familial|_11|not_provided": 3,
    "not_specified|CPA6-related_disorder": 1,
    "Intellectual_disability|not_provided|CPA6-related_disorder|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11": 1,
    "CPA6-related_disorder|Self-limited_epilepsy_with_centrotemporal_spikes|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|not_specified|not_provided|Global_developmental_delay|Epilepsy|Periventricular_heterotopia|Palpitations|Confusion|Irregular_menstruation|Abnormal_emotional_state|Seizure|Focal-onset_seizure": 1,
    "Febrile_seizures|_familial|_11|Familial_temporal_lobe_epilepsy_5": 8,
    "not_provided|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|not_specified": 1,
    "not_provided|Febrile_seizures|_familial|_11": 4,
    "not_provided|not_specified|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|Self-limited_epilepsy_with_centrotemporal_spikes|Abnormal_emotional_state|Periventricular_heterotopia|Confusion|Palpitations|Irregular_menstruation|Seizure|Focal-onset_seizure|Global_developmental_delay|Epilepsy": 1,
    "Febrile_seizures|_familial|_11|Self-limited_epilepsy_with_centrotemporal_spikes|Intellectual_disability": 1,
    "not_specified|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|not_provided": 1,
    "not_specified|not_provided|Familial_temporal_lobe_epilepsy_5": 1,
    "not_provided|not_specified|Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11": 1,
    "Familial_temporal_lobe_epilepsy_5|Febrile_seizures|_familial|_11|not_provided|not_specified": 1,
    "not_provided|Febrile_seizures|_familial|_11|Familial_temporal_lobe_epilepsy_5": 1,
    "not_provided|CPA6-related_disorder|Familial_temporal_lobe_epilepsy_2": 1,
    "Familial_temporal_lobe_epilepsy_2": 2,
    "not_provided|PREX2-related_disorder": 8,
    "PREX2-related_disorder": 29,
    "PREX2-related_disorder|not_specified": 1,
    "PREX2-related_disorder|not_provided": 5,
    "PREX2-related_disorder|not_specified|not_provided": 1,
    "SULF1-related_disorder|not_provided": 1,
    "not_provided|SULF1-related_disorder": 2,
    "SULF1-related_disorder": 2,
    "SLCO5A1-related_disorder|not_provided": 2,
    "LACTB2-related_condition": 1,
    "Otofaciocervical_syndrome_1|Branchiootorenal_Spectrum_Disorders": 6,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 31,
    "not_provided|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 5,
    "Branchiootorenal_Spectrum_Disorders|Otofaciocervical_syndrome_1": 7,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 22,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1": 3,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_provided": 2,
    "not_provided|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "not_provided|EYA1-related_disorder": 1,
    "EYA1-related_disorder": 11,
    "Branchiootorenal_syndrome_1": 50,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|not_provided|not_specified": 2,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|not_provided|Focal_segmental_glomerulosclerosis|Rare_genetic_deafness": 1,
    "not_specified|Melnick-Fraser_syndrome": 2,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|Inborn_genetic_diseases": 1,
    "Melnick-Fraser_syndrome|EYA1-related_disorder|Inborn_genetic_diseases": 1,
    "Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1": 2,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_provided|not_specified|Melnick-Fraser_syndrome": 1,
    "Melnick-Fraser_syndrome|not_specified|not_provided|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "not_provided|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1": 1,
    "Otofaciocervical_syndrome_1": 4,
    "Melnick-Fraser_syndrome|Branchiootorenal_syndrome_1": 4,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 40,
    "Inborn_genetic_diseases|Melnick-Fraser_syndrome": 5,
    "Branchiootic_syndrome_1": 16,
    "Anterior_segment_anomalies_and_cataract": 1,
    "Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|not_specified": 1,
    "Branchiootic_syndrome_1|Melnick-Fraser_syndrome|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|EYA1-related_disorder|Melnick-Fraser_syndrome": 1,
    "Bilateral_renal_agenesis|Anhydramnios": 1,
    "Melnick-Fraser_syndrome|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 2,
    "not_provided|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 2,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Melnick-Fraser_syndrome|EYA1-related_disorder": 2,
    "Rare_genetic_deafness|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 1,
    "not_provided|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 1,
    "not_provided|Melnick-Fraser_syndrome": 11,
    "EYA1-related_disorder|Melnick-Fraser_syndrome|not_specified|not_provided|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Developmental_cataract": 1,
    "Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 2,
    "Melnick-Fraser_syndrome|EYA1-related_disorder|Branchiootorenal_syndrome_1": 1,
    "Inborn_genetic_diseases|Melnick-Fraser_syndrome|not_provided": 1,
    "Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|not_specified": 2,
    "Melnick-Fraser_syndrome|not_specified": 3,
    "Melnick-Fraser_syndrome|Inborn_genetic_diseases": 1,
    "Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Melnick-Fraser_syndrome|not_specified|not_provided": 1,
    "Melnick-Fraser_syndrome|Branchiootic_syndrome_1": 2,
    "Hereditary_ataxia|Melnick-Fraser_syndrome|EYA1-related_disorder": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|not_specified": 2,
    "Melnick-Fraser_syndrome|EYA1-related_disorder|Rare_genetic_deafness|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Branchiooculofacial_syndrome": 1,
    "Melnick-Fraser_syndrome|not_specified|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1": 2,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Melnick-Fraser_syndrome|not_provided|not_specified": 1,
    "Melnick-Fraser_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Branchiootic_syndrome_1|Branchiootorenal_syndrome_with_cataract|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|not_specified|not_provided": 2,
    "Melnick-Fraser_syndrome|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|not_specified": 1,
    "EYA1-related_disorder|Melnick-Fraser_syndrome": 2,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_provided|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|not_specified": 1,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_1": 1,
    "Melnick-Fraser_syndrome|not_specified|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|not_provided|Branchiootorenal_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1": 2,
    "Abnormal_anterior_chamber_morphology": 1,
    "Melnick-Fraser_syndrome|EYA1-related_disorder|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Branchiootorenal_syndrome_1|not_provided": 1,
    "Branchiootic_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|EYA1-related_disorder|not_provided": 1,
    "not_provided|Melnick-Fraser_syndrome|Branchiootorenal_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|not_specified|Branchiootorenal_syndrome_1|not_provided": 1,
    "Melnick-Fraser_syndrome|Rare_genetic_deafness|Branchiootorenal_syndrome_1|EYA1-related_disorder|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_provided": 1,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_specified|not_provided|EYA1-related_disorder": 1,
    "Melnick-Fraser_syndrome|not_provided|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|EYA1-related_disorder": 1,
    "not_provided|EYA1-related_disorder|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Inborn_genetic_diseases|not_provided|EYA1-related_disorder": 1,
    "Branchiootorenal_syndrome_1|Inborn_genetic_diseases|Melnick-Fraser_syndrome|not_provided": 1,
    "Hearing_impairment|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Melnick-Fraser_syndrome|not_specified|not_provided": 1,
    "EYA1-related_disorder|Melnick-Fraser_syndrome|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_specified|not_provided": 1,
    "not_specified|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "not_provided|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|not_specified|Melnick-Fraser_syndrome": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Melnick-Fraser_syndrome|not_provided": 1,
    "not_provided|not_specified|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Melnick-Fraser_syndrome": 1,
    "not_specified|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Melnick-Fraser_syndrome": 1,
    "EYA1-related_disorder|not_provided": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|not_provided|Serpentine_fibula_with_polycystic_kidney_disease|common_Congenital_Anomalies_of_the_Kidney_and_Urinary_Tract_(CAKUT)": 1,
    "EYA1-related_disorder|not_provided|Melnick-Fraser_syndrome": 1,
    "Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|not_provided": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_provided": 1,
    "not_specified|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts": 7,
    "not_provided|Melnick-Fraser_syndrome|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|not_provided|Otofaciocervical_syndrome_1": 1,
    "not_provided|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1": 1,
    "not_provided|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Melnick-Fraser_syndrome": 1,
    "EYA1-related_disorder|Melnick-Fraser_syndrome|not_provided": 1,
    "not_specified|not_provided|Melnick-Fraser_syndrome": 1,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|not_provided": 1,
    "not_provided|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "not_provided|not_specified|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Melnick-Fraser_syndrome|not_provided": 1,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|not_specified|not_provided|EYA1-related_disorder|Melnick-Fraser_syndrome": 1,
    "Melnick-Fraser_syndrome|not_specified|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|not_provided": 1,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|EYA1-related_disorder|not_specified": 1,
    "not_provided|Melnick-Fraser_syndrome|EYA1-related_disorder": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "Melnick-Fraser_syndrome|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Inborn_genetic_diseases": 1,
    "EYA1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Melnick-Fraser_syndrome|not_provided|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1": 1,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|not_provided": 1,
    "Melnick-Fraser_syndrome|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|not_provided": 1,
    "not_provided|EYA1-related_disorder|Melnick-Fraser_syndrome": 1,
    "Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Melnick-Fraser_syndrome|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|not_specified|not_provided": 1,
    "not_provided|Branchiootic_syndrome_1|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Melnick-Fraser_syndrome": 2,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|not_provided": 1,
    "Melnick-Fraser_syndrome|Renal_hypoplasia": 1,
    "Melnick-Fraser_syndrome|EYA1-related_disorder|Inborn_genetic_diseases|Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|not_specified|not_provided": 1,
    "Branchiootorenal_syndrome_1|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1": 1,
    "Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Otofaciocervical_syndrome_1|Branchiootic_syndrome_1|Melnick-Fraser_syndrome|not_specified": 1,
    "not_provided|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1|Branchiootorenal_syndrome_1|Melnick-Fraser_syndrome": 1,
    "Melnick-Fraser_syndrome|not_specified|Otofaciocervical_syndrome_1|EYA1-related_disorder": 1,
    "Melnick-Fraser_syndrome|not_provided|Inborn_genetic_diseases|Branchiootorenal_syndrome_1|Branchiootic_syndrome_1|Otofaciocervical_syndrome_1": 1,
    "Otofaciocervical_syndrome_1|Branchiootorenal_Spectrum_Disorders|not_provided": 1,
    "Familial_episodic_pain_syndrome_with_predominantly_upper_body_involvement|not_provided|TRPA1-related_disorder": 1,
    "TRPA1-related_disorder|not_provided": 3,
    "Familial_episodic_pain_syndrome_with_predominantly_upper_body_involvement|not_provided": 9,
    "TRPA1-related_disorder": 19,
    "Familial_episodic_pain_syndrome_with_predominantly_upper_body_involvement": 9,
    "Familial_episodic_pain_syndrome_with_predominantly_upper_body_involvement|not_specified": 3,
    "not_provided|Familial_episodic_pain_syndrome_with_predominantly_upper_body_involvement": 1,
    "KCNB2-related_disorder": 5,
    "KCNB2-related_disorder|not_provided": 3,
    "KCNB2-associated_neurodevelopmental_disorder": 2,
    "TERF1-related_disorder": 2,
    "Mitochondrial_proton-transporting_ATP_synthase_complex_deficiency": 1,
    "not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 23,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 245,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|Inborn_genetic_diseases": 12,
    "not_specified|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 3,
    "Inborn_genetic_diseases|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 5,
    "Autosomal_recessive_disease": 1,
    "not_specified|TMEM70-related_disorder|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 1,
    "not_specified|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 7,
    "Mitochondrial_proton-transporting_ATP_synthase_complex_deficiency|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|not_provided": 2,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|not_provided": 5,
    "Autosomal_recessive_disease|not_specified|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|not_specified": 2,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|TMEM70-related_disorder": 2,
    "TMEM70-related_disorder|Neurodevelopmental_disorder|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|See_cases": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2|TMEM70-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_2": 1,
    "Congenital_myopathy|Congenital_myopathy_25": 4,
    "JPH1-related_disorder": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2K": 14,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    ".|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease_type_4A": 228,
    "Charcot-Marie-Tooth_with_Vocal_Cord_Paresis|Charcot-Marie-Tooth|_Intermediate|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 5,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K": 15,
    "not_provided|Charcot-Marie-Tooth_disease_type_4A": 16,
    "Charcot-Marie-Tooth_disease_type_4A|not_provided": 11,
    "not_specified|Charcot-Marie-Tooth_disease_type_4A": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4A": 2,
    "Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4A": 9,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4A|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2K|Charcot-Marie-Tooth_disease": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4A": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4A": 2,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K": 3,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease_type_4A|not_specified|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease": 11,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A": 2,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K": 5,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 26,
    "Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_with_Vocal_Cord_Paresis|Charcot-Marie-Tooth|_Intermediate|Inborn_genetic_diseases|GDAP1-related_disorder|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Pes_cavus|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A|GDAP1-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_type_4A": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K|Peripheral_neuropathy|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A": 2,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 3,
    "Charcot-Marie-Tooth_disease_type_4A|not_specified|not_provided": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4A|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|not_provided|Neuropathy|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_type_4A|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2K": 1,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2K|Charcot-Marie-Tooth_disease_axonal_type_2K": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_type_4A|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A|not_specified|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease_type_4A|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_4A": 1,
    "GDAP1-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided|Sensory_neuropathy|Elevated_circulating_creatine_kinase_concentration|Peripheral_axonal_neuropathy|Elevated_circulating_alkaline_phosphatase_concentration|Polyneuropathy": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_specified|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_type_4A": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2K|Tip-toe_gait|Charcot-Marie-Tooth_disease_type_4A": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|not_provided": 1,
    "GDAP1-related_disorder|Charcot-Marie-Tooth_disease_type_4A|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4A|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided": 1,
    "GDAP1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Neuropathy|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_axonal_type_2K|Charcot-Marie-Tooth_disease_type_4A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2K": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2K|not_provided|Charcot-Marie-Tooth_disease_type_4A": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease_type_4A|not_provided|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 33,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided": 2,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A|not_provided": 2,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_A|not_provided|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 5,
    "Charcot-Marie-Tooth|_Intermediate|Charcot-Marie-Tooth_with_Vocal_Cord_Paresis": 1,
    "Charcot-Marie-Tooth|_Intermediate|Charcot-Marie-Tooth_with_Vocal_Cord_Paresis|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_A|Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive": 2,
    "Charcot-Marie-Tooth_disease|_axonal|_with_vocal_cord_paresis|_autosomal_recessive|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_A": 1,
    "Charcot-Marie-Tooth_with_Vocal_Cord_Paresis|Charcot-Marie-Tooth|_Intermediate": 5,
    "GDAP1-related_disorder": 1,
    "Benign_concentric_annular_macular_dystrophy|Vitelliform_macular_dystrophy_4": 2,
    "ZFHX4-related_disorder": 47,
    "ZFHX4-related_disorder|not_provided": 5,
    "not_provided|ZFHX4-related_disorder": 7,
    "Ptosis|_hereditary_congenital|_1": 4,
    "not_specified|Ptosis|_hereditary_congenital|_1": 2,
    "not_provided|Ptosis|_hereditary_congenital|_1": 3,
    "Congenital_corneal_opacity": 1,
    "not_specified|ZFHX4-related_disorder": 4,
    "ZFHX4-related_disorder|not_specified|not_provided": 1,
    "Usher_syndrome_type_1F": 300,
    "ZFHX4-associated_neurodevelopmental_disorder": 1,
    "ZFHX4-related_syndrome": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)": 330,
    "not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 20,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B": 15,
    "not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Zellweger_spectrum_disorders|PEX2-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|PEX2-related_disorder": 2,
    "not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_5B": 3,
    "Peroxisome_biogenesis_disorder_5B|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 8,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|PEX2-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_5B|See_cases": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|not_specified|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|not_provided": 5,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Zellweger_spectrum_disorders": 8,
    "not_provided|Zellweger_spectrum_disorders|not_specified|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Inborn_genetic_diseases|PEX2-related_disorder|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 6,
    "PEX2-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)|not_provided|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 7,
    "PEX2-related_disorder|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 2,
    "PEX2-related_disorder": 3,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B": 2,
    "not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Inborn_genetic_diseases": 1,
    "PEX2-related_disorder|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Zellweger_spectrum_disorders": 1,
    "Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "See_cases|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Zellweger_spectrum_disorders|PEX2-related_disorder|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Zellweger_spectrum_disorders|Inborn_genetic_diseases": 1,
    "not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "PEX2-related_disorder|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|not_provided|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|PEX2-related_disorder|Zellweger_spectrum_disorders|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Zellweger_spectrum_disorders|PEX2-related_disorder": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "PEX2-related_disorder|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Inborn_genetic_diseases|Zellweger_spectrum_disorders|not_provided": 1,
    "not_provided|PEX2-related_disorder|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "PEX2-related_disorder|not_specified|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|not_specified": 1,
    "Peroxisome_biogenesis_disorder_5B|Peroxisome_biogenesis_disorder": 1,
    "Inborn_genetic_diseases|Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|Inborn_genetic_diseases|Zellweger_spectrum_disorders": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_5A_(Zellweger)|PEX2-related_disorder|Inborn_genetic_diseases": 1,
    "Zellweger_spectrum_disorders|PEX2-related_disorder|Peroxisome_biogenesis_disorder_5A_(Zellweger)|Peroxisome_biogenesis_disorder_5B|not_specified|not_provided": 1,
    "Zellweger_spectrum_disorders|not_provided|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_5A_(Zellweger)": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_5|IL7-related_disorder": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_5": 4,
    "not_provided|IL7-related_disorder": 1,
    "IL7-related_disorder": 1,
    "IL7-related_disorder|not_provided": 1,
    "HEY1-related_disorder": 8,
    "not_provided|HEY1-related_disorder": 1,
    "HEY1-related_disorder|not_provided": 1,
    "MRPS28-related_disorder": 8,
    "Combined_oxidative_phosphorylation_deficiency_47": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_type_1G": 2,
    "PMP2-related_disorder|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_1E": 2,
    "not_provided|PMP2-related_disorder": 4,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1G|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1G": 5,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1G|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_type_1G|Peripheral_neuropathy|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_59": 4,
    "Intellectual_disability|_autosomal_recessive_59|not_specified": 1,
    "not_provided|IMPA1-related_disorder": 1,
    "Carbonic_anhydrase_I|_Guam": 1,
    "Carbonic_anhydrase_I_deficiency": 1,
    "Renal_tubular_acidosis|Rickets|Metabolic_acidosis": 1,
    "not_provided|Osteopetrosis_with_renal_tubular_acidosis": 20,
    "Osteopetrosis_with_renal_tubular_acidosis": 54,
    "CA2-related_disorder|not_provided|Osteopetrosis_with_renal_tubular_acidosis": 1,
    "Inborn_genetic_diseases|Osteopetrosis_with_renal_tubular_acidosis": 3,
    "CARBONIC_ANHYDRASE_II_VARIANT": 2,
    "not_provided|CA2-related_disorder|Osteopetrosis_with_renal_tubular_acidosis": 1,
    "Osteopetrosis_with_renal_tubular_acidosis|Inborn_genetic_diseases": 3,
    "CA2-related_disorder": 2,
    "not_provided|CA2-related_disorder": 1,
    "not_provided|Osteopetrosis|Osteopetrosis_with_renal_tubular_acidosis": 1,
    "Osteopetrosis_with_renal_tubular_acidosis|not_provided|Inborn_genetic_diseases": 1,
    "Osteopetrosis_with_renal_tubular_acidosis|not_provided": 5,
    "Inborn_genetic_diseases|Osteopetrosis_with_renal_tubular_acidosis|not_provided": 1,
    "not_specified|not_provided|Osteopetrosis_with_renal_tubular_acidosis": 1,
    "Osteopetrosis_with_renal_tubular_acidosis|Neurodevelopmental_delay": 1,
    "Inborn_genetic_diseases|not_provided|Osteopetrosis_with_renal_tubular_acidosis": 1,
    "CA2-related_disorder|not_provided": 1,
    "not_provided|Osteopetrosis_with_renal_tubular_acidosis|CARBONIC_ANHYDRASE_II_VARIANT": 1,
    "not_provided|Stargardt_Disease|_Recessive|Achromatopsia": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 32,
    "Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|not_provided": 3,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 2,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 15,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 4,
    "Stargardt_Disease|_Recessive|Achromatopsia": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Inborn_genetic_diseases": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia|Retinal_dystrophy|Achromatopsia_3|not_specified": 1,
    "not_provided|Achromatopsia": 37,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided|Achromatopsia_3": 5,
    "not_specified|Achromatopsia|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 4,
    "Retinal_dystrophy|Achromatopsia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Achromatopsia": 5,
    "Achromatopsia|not_provided|Retinal_dystrophy|Achromatopsia_3": 1,
    "CNGB3-related_retinopathy": 2,
    "not_provided|CNGB3-related_disorder": 1,
    "Achromatopsia_3": 79,
    "Retinal_dystrophy|Achromatopsia|not_provided|Inborn_genetic_diseases": 1,
    "Achromatopsia_3|not_provided|Achromatopsia": 3,
    "Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Retinal_dystrophy|not_provided": 1,
    "Achromatopsia_3|not_provided": 19,
    "Inborn_genetic_diseases|Achromatopsia|not_provided": 3,
    "Achromatopsia|not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 5,
    "not_provided|Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "Achromatopsia_3|not_provided|Achromatopsia|Inborn_genetic_diseases": 1,
    "CNGB3-related_retinopathy|not_provided|Inborn_genetic_diseases|Achromatopsia": 1,
    "not_provided|Achromatopsia_3|Retinal_dystrophy": 1,
    "not_specified|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Achromatopsia": 1,
    "not_provided|Achromatopsia_3": 32,
    "CNGB3-related_disorder|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia|Achromatopsia_3": 1,
    "not_provided|Macular_dystrophy|Achromatopsia_3": 1,
    "Achromatopsia|not_provided|Achromatopsia_3": 4,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy|Inborn_genetic_diseases|Achromatopsia|not_provided": 1,
    "not_provided|Achromatopsia_3|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|CNGB3-related_disorder|Achromatopsia_3|not_provided": 1,
    "not_provided|Achromatopsia|Achromatopsia_3": 3,
    "CNGB3-related_retinopathy|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Retinal_dystrophy|not_provided": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|not_provided|Achromatopsia_3|Achromatopsia": 1,
    "Achromatopsia|Severe_early-childhood-onset_retinal_dystrophy|not_provided|Achromatopsia_3": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Achromatopsia": 1,
    "Achromatopsia_3|Achromatopsia|not_provided|CNGB3-related_disorder|Abnormality_of_the_eye": 1,
    "Achromatopsia_3|Achromatopsia": 1,
    "Achromatopsia|not_provided|not_specified|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 1,
    "Retinal_dystrophy|not_provided|Achromatopsia_3": 1,
    "Retinal_dystrophy|not_provided|Achromatopsia": 1,
    "Achromatopsia|CNGB3-related_retinopathy|not_provided|CNGB3-related_disorder": 1,
    "Achromatopsia_3|not_provided|Inborn_genetic_diseases|Achromatopsia": 1,
    "Achromatopsia|Achromatopsia_3": 4,
    "Retinitis_pigmentosa|Achromatopsia_3|not_provided|Achromatopsia": 1,
    "Retinal_dystrophy|Achromatopsia|Achromatopsia_3|not_provided": 1,
    "not_provided|Achromatopsia_3|Achromatopsia": 2,
    "Achromatopsia|not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 4,
    "Achromatopsia_3|Achromatopsia|not_provided": 1,
    "Retinal_dystrophy|Achromatopsia|Achromatopsia_3": 1,
    "CNGB3-related_disorder|Retinal_dystrophy|Achromatopsia|not_provided|Achromatopsia_3": 1,
    "Achromatopsia|not_specified|not_provided|Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 3,
    "not_provided|Achromatopsia|Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Achromatopsia|not_provided": 1,
    "Achromatopsia|not_provided|Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy|CNGB3-related_disorder|Achromatopsia|not_provided": 1,
    "CNGB3-related_disorder|not_specified|not_provided|Achromatopsia": 1,
    "Retinal_dystrophy|Achromatopsia|not_provided|Achromatopsia_3": 2,
    "Achromatopsia|Inborn_genetic_diseases|not_provided": 3,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia|not_specified|not_provided": 1,
    "not_provided|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia|Achromatopsia_3": 2,
    "not_provided|Abnormality_of_the_eye|Achromatopsia_3|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Achromatopsia|not_specified|not_provided|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Abnormality_of_the_eye": 1,
    "CNGB3-related_disorder|Achromatopsia|not_provided": 1,
    "not_provided|Achromatopsia_3|not_specified": 1,
    "Achromatopsia|not_specified|not_provided": 1,
    "Achromatopsia|Achromatopsia_3|not_provided": 2,
    "not_provided|Achromatopsia|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 2,
    "CNGB3-related_disorder|Retinal_dystrophy|Inborn_genetic_diseases|Optic_atrophy|Achromatopsia|Retinitis_pigmentosa|Cone-rod_dystrophy|not_provided|Achromatopsia_3|Leber_congenital_amaurosis|Abnormality_of_the_eye": 1,
    "Achromatopsia_3|not_provided|Retinal_dystrophy": 1,
    "Achromatopsia|Retinal_dystrophy|Achromatopsia_3|not_provided": 1,
    "not_provided|Achromatopsia_3|CNGB3-related_retinopathy|Retinal_dystrophy|Achromatopsia": 1,
    "not_provided|Achromatopsia_3|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Achromatopsia|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|Retinal_dystrophy|not_provided": 1,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy|not_specified|Achromatopsia|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Achromatopsia": 1,
    "not_provided|Retinal_dystrophy|Achromatopsia_3": 1,
    "CNGB3-related_disorder|Retinal_dystrophy|not_provided|Achromatopsia_3": 1,
    "Achromatopsia|not_provided|Abnormal_electroretinogram|Nystagmus|Retinal_dystrophy|Leber_congenital_amaurosis|Achromatopsia_3": 1,
    "Achromatopsia|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Achromatopsia_3": 1,
    "not_specified|not_provided|Achromatopsia_3|Achromatopsia": 1,
    "CNGB3-related_disorder|Achromatopsia_3|Retinitis_pigmentosa|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia|not_provided": 1,
    "Achromatopsia|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3|not_provided": 1,
    "Achromatopsia|not_provided|CNGB3-related_disorder|Retinal_dystrophy|CNGB3-related_retinopathy": 1,
    "Stargardt_Disease|_Recessive|Achromatopsia|not_provided": 1,
    "not_provided|Achromatopsia|Inborn_genetic_diseases": 1,
    "Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Achromatopsia_3|Achromatopsia|not_provided": 1,
    "not_specified|not_provided|Stargardt_Disease|_Recessive|Achromatopsia": 1,
    "CNGB3-related_disorder|not_provided|Achromatopsia|Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Stargardt_Disease|_Recessive|Retinal_dystrophy|Achromatopsia|not_provided": 1,
    "not_specified|not_provided|Achromatopsia_3|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Achromatopsia|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Achromatopsia|Severe_early-childhood-onset_retinal_dystrophy|Achromatopsia_3": 1,
    "CNGB3-related_disorder|not_provided|Achromatopsia": 1,
    "DCAF4L2-related_disorder": 10,
    "not_provided|DCAF4L2-related_disorder": 1,
    "not_specified|DCAF4L2-related_disorder": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency": 1193,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 37,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 38,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 360,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 430,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 33,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 18,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 3,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 32,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 22,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified": 22,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 12,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 17,
    "not_provided|not_specified|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 14,
    "Malignant_tumor_of_breast|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified": 19,
    "Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 36,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "NBN-related_disorder|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 29,
    "Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 3,
    "NBN-related_disorder|not_provided|Malignant_tumor_of_breast|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia": 9,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 31,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 19,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 12,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 16,
    "Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia": 12,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 2,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 23,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 11,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 10,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 3,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided": 3,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|Aplastic_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder": 1,
    "Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 3,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|not_specified": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome": 18,
    "not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 5,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 16,
    "not_specified|NBN-related_disorder|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 3,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 3,
    "Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 6,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Acute_lymphoid_leukemia|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 5,
    "NBN-related_disorder|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|NBN-related_disorder|Aplastic_anemia": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_specified|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|NBN-related_disorder": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Acute_lymphoid_leukemia": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|Aplastic_anemia|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "not_provided|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "Gastric_cancer|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|NBN-related_disorder|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia": 1,
    "NBN-related_disorder|Aplastic_anemia|not_provided|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|not_specified": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 2,
    "Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia": 2,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia": 3,
    "Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "not_specified|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "NBN-related_disorder|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 7,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Breast_and/or_ovarian_cancer": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 3,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastric_cancer|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia": 1,
    "Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 1,
    "Familial_cancer_of_breast|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 6,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|not_specified|not_provided": 2,
    "not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 2,
    "NBN-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer|NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Aplastic_anemia|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_provided|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_lymphoma|_large_B-cell|_diffuse|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified": 12,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder|Aplastic_anemia|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|NBN-related_disorder|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 4,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|not_specified|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder|not_specified|Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia": 4,
    "not_provided|not_specified|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|NBN-related_disorder|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 3,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 3,
    "Malignant_tumor_of_breast|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Familial_cancer_of_breast|not_provided|Aplastic_anemia|Acute_lymphoid_leukemia": 1,
    "not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|not_provided": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_carcinoma|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Ovarian_carcinoma|Aplastic_anemia": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 6,
    "NBN-related_disorder|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Acute_lymphoid_leukemia": 1,
    "Malignant_tumor_of_breast|NBN-related_disorder|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_provided": 2,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 3,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_carcinoma|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Prostate_cancer|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia": 1,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "NBN-related_disorder|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 5,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Breast_carcinoma": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|Aplastic_anemia": 1,
    "not_specified|Malignant_tumor_of_breast|NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Aplastic_anemia|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|NBN-related_disorder|Aplastic_anemia|Acute_lymphoid_leukemia": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 16,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Gastric_cancer": 1,
    "Aplastic_anemia|NBN-related_disorder|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Premature_ovarian_insufficiency|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "Hereditary_cancer|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|NBN-related_disorder|not_provided": 1,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Hereditary_cancer|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|NBN-related_disorder|not_specified|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "NBN-related_disorder|not_specified|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "NBN-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|not_provided": 1,
    "Malignant_tumor_of_breast|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Gastric_cancer|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 2,
    "NBN-related_disorder|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder": 1,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Aplastic_anemia|Acute_lymphoid_leukemia": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency|Familial_cancer_of_breast|Aplastic_anemia|Acute_lymphoid_leukemia|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|not_provided|Hepatocellular_carcinoma|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Microcephaly|Lissencephaly|Breast_carcinoma": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "NBN-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|Acute_lymphoid_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 2,
    "not_provided|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|not_specified": 1,
    "Pediatric_high-grade_glioma|Diffuse_midline_glioma|_H3_K27-altered|NBN-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|Leukemia|_acute_lymphoblastic|_susceptibility_to|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Carcinoma_of_colon|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|not_specified": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|NBN-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "NBN-related_disorder": 2,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "NBN-related_disorder|Microcephaly|_normal_intelligence_and_immunodeficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|NBN-related_disorder": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Prostate_cancer": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|not_provided|Acute_lymphoid_leukemia": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|Acute_lymphoid_leukemia|not_specified": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "NBN-related_disorder|Acute_lymphoid_leukemia|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|See_cases|not_provided": 1,
    "Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Aplastic_anemia|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 2,
    "Gastric_cancer|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Acute_lymphoid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "NBN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided|Acute_lymphoid_leukemia": 1,
    "not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Prostate_cancer_susceptibility|Lymphoma|not_provided|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|not_provided": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|Aplastic_anemia|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Microcephaly|_normal_intelligence_and_immunodeficiency|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Acute_lymphoid_leukemia|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Microcephaly|_normal_intelligence_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Aplastic_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Aplastic_anemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Acute_lymphoid_leukemia|not_provided": 1,
    "Acute_lymphoid_leukemia|Microcephaly|_normal_intelligence_and_immunodeficiency|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|Malignant_tumor_of_breast|Aplastic_anemia|Acute_lymphoid_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Microcephaly|_normal_intelligence_and_immunodeficiency|NBN-related_disorder|not_provided": 1,
    "DECR1-related_disorder": 3,
    "Progressive_encephalopathy_with_leukodystrophy_due_to_DECR_deficiency|not_provided|DECR1-related_disorder": 1,
    "OTUD6B-related_disorder|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies": 1,
    "OTUD6B-related_disorder": 3,
    "OTUD6B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|Intellectual_disability|Epilepsy|Dysmorphic_features": 2,
    "Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|not_provided": 4,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|Epilepsy|Intellectual_disability|Dysmorphic_features|Inborn_genetic_diseases": 1,
    "not_provided|OTUD6B-related_disorder": 1,
    "Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|not_provided|Intellectual_disability|Epilepsy|Dysmorphic_features": 1,
    "OTUD6B-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|not_specified": 1,
    "not_provided|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|Intellectual_disability|not_provided": 1,
    "OTUD6B-related_disorder|Intellectual_developmental_disorder_with_dysmorphic_facies|_seizures|_and_distal_limb_anomalies|not_provided": 1,
    "SLC26A7-related_disorder": 1,
    "RUNX1T1-related_disorder": 6,
    "not_provided|PPP1R13B_related_disorder": 1,
    "not_provided|RUNX1T1-related_disorder": 4,
    "RUNX1-IT1_related_disorder": 1,
    "RUNX1T1-related_disorder|not_provided": 1,
    "RUNX1T1-associated_neurodevelopmental_disorder": 1,
    "CIBAR1-related_disorder": 3,
    "Polydactyly|_postaxial|_type_A9": 2,
    "Polydactyly|_postaxial|_type_A9|Postaxial_polydactyly_type_A": 1,
    "TMEM67-related_disorder|Nephronophthisis|not_specified|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "TMEM67-related_disorder|not_provided|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3": 1,
    "Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14": 3,
    "Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "TMEM67-related_disorder": 33,
    "COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11|Bardet-Biedl_syndrome_14|TMEM67-related_disorder|not_specified|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_1": 1,
    "COACH_syndrome_1|Joubert_syndrome_6|RHYNS_syndrome|Nephronophthisis_11|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_6|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Nephronophthisis_11|RHYNS_syndrome|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Inborn_genetic_diseases|TMEM67-related_disorder": 1,
    "Nephronophthisis_11|Meckel_syndrome|_type_3|RHYNS_syndrome|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|not_provided|Joubert_syndrome_and_related_disorders|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Meckel_syndrome|_type_3|COACH_syndrome_1|RHYNS_syndrome|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "not_provided|TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome_6": 3,
    "COACH_syndrome_1|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|TMEM67-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Meckel_syndrome|_type_3": 49,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 28,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3": 2,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome_6|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Bardet-Biedl_syndrome_14|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "TMEM67-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Nephronophthisis_11": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6": 3,
    "COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 4,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome": 3,
    "Meckel_syndrome|_type_3": 22,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 10,
    "not_specified|not_provided|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_6|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders": 4,
    "Nephronophthisis_11|not_provided": 1,
    "not_specified|TMEM67-related_disorder": 1,
    "RHYNS_syndrome|Nephronophthisis_11|Joubert_syndrome_6|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_6": 24,
    "Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Joubert_syndrome_6|not_specified": 3,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6": 1,
    "Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3": 22,
    "Joubert_syndrome_6|COACH_syndrome_1|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_3|RHYNS_syndrome|COACH_syndrome_1|Joubert_syndrome_6|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_1|RHYNS_syndrome|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 4,
    "Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_specified|Meckel_syndrome|_type_3|RHYNS_syndrome|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|not_provided": 1,
    "Joubert_syndrome_6|not_provided": 2,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Meckel_syndrome|_type_3|Nephronophthisis_11|Joubert_syndrome_6": 1,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|RHYNS_syndrome": 1,
    "TMEM67-related_disorder|Atypical_hemolytic-uremic_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|RHYNS_syndrome|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_and_related_disorders|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6": 4,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Nephronophthisis_11|COACH_syndrome_1|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "RHYNS_syndrome": 3,
    "TMEM67-related_disorder|not_specified|not_provided": 1,
    "Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "not_specified|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|RHYNS_syndrome|Nephronophthisis_11": 1,
    "Joubert_syndrome_6|RHYNS_syndrome|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|not_specified": 1,
    "Joubert_syndrome_6|RHYNS_syndrome|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_14|RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|TMEM67-related_disorder|not_provided": 1,
    "Nystagmus|Iris_coloboma|Generalized_hypotonia|Cerebellar_vermis_hypoplasia|Joubert_syndrome_6|Nephronophthisis_11|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3": 1,
    "Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11": 1,
    "Nephronophthisis_11": 6,
    "Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|Inborn_genetic_diseases": 1,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Nephronophthisis_11|COACH_syndrome_1|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3": 1,
    "TMEM67-related_disorder|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_1|RHYNS_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Nephronophthisis_11|Bardet-Biedl_syndrome_14|TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders|not_provided": 1,
    "COACH_syndrome_1|Nephronophthisis_11|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders|TMEM67-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Joubert_syndrome_6": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_3|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|COACH_syndrome_1|RHYNS_syndrome": 1,
    "Joubert_syndrome_6|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|not_specified": 2,
    "Multiple_renal_cysts|Enlarged_kidney|Anhydramnios": 1,
    "TMEM67-related_disorder|Joubert_syndrome_and_related_disorders|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_3|Joubert_syndrome_6": 1,
    "not_specified|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Bardet-Biedl_syndrome_14|RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|TMEM67-related_disorder|not_provided|not_specified": 1,
    "Meckel_syndrome|_type_3|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11": 1,
    "not_provided|Kidney_failure|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome_6|COACH_syndrome_1|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Inborn_genetic_diseases|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Abnormality_of_the_nervous_system": 1,
    "COACH_syndrome_1|Meckel_syndrome|_type_3|Joubert_syndrome_6|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Joubert_syndrome_6|TMEM67-related_disorder|Nephronophthisis|Joubert_syndrome_and_related_disorders|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|COACH_syndrome_1|Nephronophthisis_11|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|TMEM67-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome_6|RHYNS_syndrome|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3|not_provided": 1,
    "COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11": 3,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Joubert_syndrome_6|TMEM67-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_specified|not_provided|Bardet-Biedl_syndrome_14|_modifier_of": 1,
    "TMEM67-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_3|COACH_syndrome_1|Joubert_syndrome_6|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|TMEM67-related_disorder": 4,
    "Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome": 1,
    "not_provided|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "RHYNS_syndrome|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Meckel_syndrome|_type_3|COACH_syndrome_1|Meckel-Gruber_syndrome|Joubert_syndrome|TMEM67-related_disorder|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|TMEM67-related_disorder": 4,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|COACH_syndrome_1|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|not_specified": 1,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6": 1,
    "TMEM67-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_1": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Nephronophthisis_11|Joubert_syndrome_6|COACH_syndrome_1|RHYNS_syndrome|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "TMEM67-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_6|COACH_syndrome_1|Meckel_syndrome|_type_3|Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14": 1,
    "not_specified|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_3": 1,
    "RHYNS_syndrome|COACH_syndrome_1|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_and_related_disorders|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_6|COACH_syndrome_1|Meckel_syndrome|_type_3|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome|Renal_cyst|Oligohydramnios|Intellectual_disability|_severe|Global_developmental_delay|Peritonitis|Kidney_damage|Nystagmus|Absent_speech|Barrel-shaped_chest|Cerebellar_vermis_hypoplasia|Cerebellar_malformation|Pancreatitis|Tremor|Visual_impairment|Floppy_infant|Congenital_ocular_coloboma|RHYNS_syndrome|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_6|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14": 1,
    "RHYNS_syndrome|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Meckel_syndrome|_type_3|COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome": 1,
    "COACH_syndrome_1|Bardet-Biedl_syndrome|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_3|RHYNS_syndrome|Nephronophthisis_11|Bardet-Biedl_syndrome_14": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|TMEM67-related_disorder": 1,
    "RHYNS_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|RHYNS_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_6|RHYNS_syndrome|COACH_syndrome_1|Meckel_syndrome|_type_3|Nephronophthisis_11|not_provided": 1,
    "TMEM67-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "TMEM67-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3": 2,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_1|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|TMEM67-related_disorder": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3": 1,
    "Joubert_syndrome_and_related_disorders|COACH_syndrome_1|RHYNS_syndrome|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|Bardet-Biedl_syndrome_14|COACH_syndrome_1|RHYNS_syndrome|Joubert_syndrome_and_related_disorders|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome_6|TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Kidney_failure|TMEM67-related_disorder|COACH_syndrome_1|RHYNS_syndrome|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Intellectual_disability": 1,
    "Joubert_syndrome_6|TMEM67-related_disorder|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_6|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_1|Joubert_syndrome_6|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|RHYNS_syndrome|Nephronophthisis_11": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3": 1,
    "COACH_syndrome_1|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|TMEM67-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Joubert_syndrome_6|Pancreatitis|Intellectual_disability|_severe|Cerebellar_vermis_hypoplasia|Tremor|Visual_impairment|Cerebellar_malformation|Peritonitis|Kidney_damage|Congenital_ocular_coloboma|Nystagmus|Absent_speech|Barrel-shaped_chest|Floppy_infant|Global_developmental_delay|TMEM67-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Oligohydramnios|Renal_cyst": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|TMEM67-related_disorder": 1,
    "Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3": 2,
    "Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|TMEM67-related_disorder": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|RHYNS_syndrome|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|TMEM67-related_disorder": 1,
    "not_provided|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|Meckel_syndrome|_type_3|RHYNS_syndrome": 1,
    "Joubert_syndrome_6|COACH_syndrome_1": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 2,
    "not_provided|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|TMEM67-related_disorder|not_provided": 1,
    "Multiple_renal_cysts|Enlarged_kidney|Anhydramnios|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_specified|Meckel_syndrome|_type_3": 1,
    "TMEM67-related_disorder|COACH_syndrome_1|not_provided|Joubert_syndrome_6|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|RHYNS_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|TMEM67-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "COACH_syndrome_1|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome_6|RHYNS_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|Meckel_syndrome|_type_3|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome_6": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|not_specified": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|not_specified|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3": 1,
    "TMEM67-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome": 1,
    "RHYNS_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Meckel_syndrome|_type_3|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|TMEM67-related_disorder": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "TMEM67-related_disorder|Kidney_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11|not_provided": 1,
    "COACH_syndrome_1|RHYNS_syndrome|Joubert_syndrome_6|Nephronophthisis_11": 1,
    "COACH_syndrome_1|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3|RHYNS_syndrome|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "TMEM67-related_disorder|Joubert_syndrome_6|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_3|Ciliopathy|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "RHYNS_syndrome|Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|Meckel_syndrome|_type_3|COACH_syndrome_1|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_6": 1,
    "TMEM67-related_disorder|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3": 1,
    "Meckel_syndrome|_type_3|not_specified": 1,
    "Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3|RHYNS_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|RHYNS_syndrome|Meckel_syndrome|_type_3|Kidney_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "COACH_syndrome_1|Joubert_syndrome_6|RHYNS_syndrome|Nephronophthisis_11|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|not_provided": 1,
    "Generalized_hypotonia|Cerebellar_vermis_hypoplasia|Iris_coloboma|Nystagmus": 1,
    "Nephronophthisis_11|Bardet-Biedl_syndrome_14|Joubert_syndrome_6|RHYNS_syndrome|Meckel_syndrome|_type_3|COACH_syndrome_1|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Nephronophthisis_11|Meckel_syndrome|_type_3|RHYNS_syndrome|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_3|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3": 1,
    "Nephronophthisis_11|Joubert_syndrome_6": 2,
    "COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome|Joubert_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome_and_related_disorders|Meckel-Gruber_syndrome|Joubert_syndrome|TMEM67-related_disorder|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_3|TMEM67-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_1": 1,
    "COACH_syndrome_1|Joubert_syndrome_6|RHYNS_syndrome|Nephronophthisis_11|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|TMEM67-related_disorder|not_provided|not_specified|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Meckel_syndrome|_type_3|Joubert_syndrome_6": 1,
    "Meckel_syndrome|_type_3|TMEM67-related_disorder": 1,
    "Kidney_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Nephronophthisis_11|RHYNS_syndrome|Meckel_syndrome|_type_3|COACH_syndrome_1|Bardet-Biedl_syndrome_14|Joubert_syndrome_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_11|COACH_syndrome_1|Bardet-Biedl_syndrome_14|RHYNS_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3": 1,
    "Joubert_syndrome_6|COACH_syndrome_1|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|Nephronophthisis_11|RHYNS_syndrome": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Nephronophthisis_11|COACH_syndrome_1|Joubert_syndrome_6|RHYNS_syndrome|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14": 1,
    "Meckel_syndrome|_type_3|Joubert_syndrome_6|COACH_syndrome_1|Nephronophthisis_11": 1,
    "Joubert_syndrome_6|not_provided|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|not_specified|Joubert_syndrome_6|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Nephronophthisis_11|COACH_syndrome_1|Meckel_syndrome|_type_3": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1|RHYNS_syndrome|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11": 1,
    "not_provided|not_specified|Nephronophthisis_11|Meckel_syndrome|_type_3|Joubert_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis_11|RHYNS_syndrome|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Joubert_syndrome_6|Meckel_syndrome|_type_3|Joubert_syndrome|Meckel-Gruber_syndrome|TMEM67-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_6|Meckel_syndrome|_type_3|Bardet-Biedl_syndrome_14|COACH_syndrome_1|Nephronophthisis_11|RHYNS_syndrome": 1,
    "Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|not_provided": 1,
    "Nephronophthisis_11|Joubert_syndrome_6|Meckel_syndrome|_type_3|not_provided|not_specified": 1,
    "Meckel_syndrome|_type_3|Joubert_syndrome_6|Nephronophthisis_11": 1,
    "not_provided|Pyruvate_dehydrogenase_phosphatase_deficiency": 3,
    "Pyruvate_dehydrogenase_phosphatase_deficiency|not_provided": 3,
    "not_provided|PDP1-related_disorder": 1,
    "Pyruvate_dehydrogenase_phosphatase_deficiency|not_specified|not_provided": 1,
    "not_provided|Non-Hodgkin_lymphoma": 1,
    "ESRP1-related_disorder|not_provided": 3,
    "ESRP1-related_disorder": 12,
    "Hearing_loss|_autosomal_recessive_109|not_provided": 2,
    "Hearing_loss|_autosomal_recessive_109": 2,
    "Hearing_loss|_autosomal_recessive_109|not_provided|ESRP1-related_disorder": 2,
    "INTS8-related_disorder": 6,
    "INTS8-related_disorder|not_provided": 4,
    "Neurodevelopmental_disorder_with_cerebellar_hypoplasia_and_spasticity": 4,
    "not_provided|Neurodevelopmental_disorder_with_cerebellar_hypoplasia_and_spasticity": 1,
    "not_provided|INTS8-related_disorder": 1,
    "Neurodevelopmental_disorder_with_cerebellar_hypoplasia_and_spasticity|INTS8-related_disorder|not_provided": 2,
    "Fanconi_renotubular_syndrome_5|Mitochondrial_complex_I_deficiency|_nuclear_type_17": 1,
    "NDUFAF6-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Fanconi_renotubular_syndrome_5|Mitochondrial_complex_I_deficiency|_nuclear_type_17": 1,
    "NDUFAF6-related_disorder|Fanconi_renotubular_syndrome_5|Mitochondrial_complex_I_deficiency|_nuclear_type_17|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17": 16,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|not_provided": 2,
    "not_provided|Fanconi_renotubular_syndrome_5": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|Fanconi_renotubular_syndrome_5": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|Leigh_syndrome|not_provided": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_17": 1,
    "NDUFAF6-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|Fanconi_renotubular_syndrome_5|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|not_specified|Fanconi_renotubular_syndrome_5|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|not_provided|Fanconi_renotubular_syndrome_5": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|not_provided|See_cases|Inborn_genetic_diseases": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_17": 2,
    "Developmental_regression|not_provided": 1,
    "not_provided|NDUFAF6-related_disorder": 1,
    "NDUFAF6-related_disorder|not_specified|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|Fanconi_renotubular_syndrome_5|not_specified|not_provided": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_17|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|NDUFAF6-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_17|not_provided|Inborn_genetic_diseases": 1,
    "Leigh_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Fanconi_renotubular_syndrome_5|Mitochondrial_complex_I_deficiency|_nuclear_type_17|not_specified|not_provided": 1,
    "Developmental_regression": 1,
    "Mitochondrial_disease|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_17": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_17|Fanconi_renotubular_syndrome_5": 1,
    "Cone-rod_dystrophy_16|Retinitis_pigmentosa": 32,
    "not_provided|Cone-rod_dystrophy_16|Retinitis_pigmentosa": 4,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_16": 10,
    "Cone-rod_dystrophy_16|not_provided|Retinitis_pigmentosa": 2,
    "Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive|not_provided": 1,
    "Cone-rod_dystrophy_16|Retinitis_pigmentosa|not_provided": 2,
    "not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_16": 1,
    "CFAP418-related_disorder": 25,
    "not_provided|CFAP418-related_disorder": 7,
    "not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_16|Bardet-biedl_syndrome_21": 5,
    "CFAP418-related_disorder|Bardet-biedl_syndrome_21|Cone-rod_dystrophy_16|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_64|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_64": 1,
    "CFAP418-related_disorder|Bardet-biedl_syndrome_21|not_provided": 1,
    "Bardet-biedl_syndrome_21|Retinal_dystrophy|not_provided|Cone-rod_dystrophy_16|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_16|Retinitis_pigmentosa": 1,
    "not_provided|Cone-rod_dystrophy_16|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa_64": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_16|Retinitis_pigmentosa": 1,
    "CFAP418-related_disorder|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_16|Bardet-biedl_syndrome_21": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_16": 1,
    "Bardet-biedl_syndrome_21|Cone-rod_dystrophy_16|Retinitis_pigmentosa|not_provided": 3,
    "not_provided|CFAP418-related_disorder|Cone-rod_dystrophy_16|Retinitis_pigmentosa|Bardet-biedl_syndrome_21": 1,
    "Cone-rod_dystrophy_16|Retinal_dystrophy": 1,
    "CFAP418-related_disorder|not_provided": 11,
    "Cone-rod_dystrophy_16": 3,
    "CFAP418-related_disorder|not_provided|Retinal_dystrophy": 1,
    "CFAP418-related_disorder|Retinal_dystrophy|not_provided|Bardet-biedl_syndrome_21|Retinitis_pigmentosa|Cone-rod_dystrophy_16": 1,
    "Bardet-biedl_syndrome_21": 3,
    "not_provided|CFAP418-related_disorder|Cone-rod_dystrophy_16|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "CFAP418-related_disorder|Cone-rod_dystrophy_16|Retinitis_pigmentosa|Bardet-biedl_syndrome_21|not_provided": 1,
    "Retinitis_pigmentosa_64|CFAP418-related_disorder": 1,
    "Bardet-biedl_syndrome_21|Cone-rod_dystrophy_16|Retinitis_pigmentosa|not_provided|CFAP418-related_disorder": 1,
    "Cone-rod_dystrophy_16|Retinitis_pigmentosa|Bardet-biedl_syndrome_21|not_provided": 3,
    "Cone-rod_dystrophy_16|Bardet-biedl_syndrome_21|Retinitis_pigmentosa|not_provided": 1,
    "Cone-rod_dystrophy_16|not_provided": 1,
    "CFAP418-related_disorder|Retinitis_pigmentosa|Cone-rod_dystrophy_16|Bardet-biedl_syndrome_21|not_provided": 2,
    "Bardet-biedl_syndrome_21|Retinitis_pigmentosa|Cone-rod_dystrophy_16": 2,
    "not_specified|Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_16": 1,
    "not_provided|Cone-rod_dystrophy_16": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|not_specified|Cone-rod_dystrophy_16": 1,
    "Retinitis_Pigmentosa|_Recessive|Cone-Rod_Dystrophy|_Recessive": 1,
    "Klippel-Feil_syndrome": 8,
    "Klippel-Feil_syndrome_1|_autosomal_dominant": 49,
    "not_provided|Klippel-Feil_syndrome_1|_autosomal_dominant": 4,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|not_provided": 9,
    "not_provided|Klippel-Feil_syndrome": 3,
    "Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17": 8,
    "Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant": 7,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4": 19,
    "Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 23,
    "Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6": 8,
    "Multiple_synostoses_syndrome_4": 2,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|not_provided": 2,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 97,
    "Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant": 3,
    "Inborn_genetic_diseases|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Multiple_synostoses_syndrome_4": 2,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|GDF6-related_disorder": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17": 6,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Inborn_genetic_diseases": 3,
    "Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Multiple_synostoses_syndrome_4|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Autosomal_dominant_Parkinson_disease_8|Klippel-Feil_syndrome": 1,
    "not_provided|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6": 8,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17": 9,
    "Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6": 17,
    "Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant": 3,
    "Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17": 20,
    "Inborn_genetic_diseases|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4": 10,
    "Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant": 2,
    "Inborn_genetic_diseases|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4": 2,
    "Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4": 15,
    "not_specified|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 2,
    "GDF6-related_disorder": 2,
    "Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant": 16,
    "Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6": 5,
    "GDF6-related_disorder|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|not_specified|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|not_provided": 1,
    "Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4": 5,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|not_specified": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4": 3,
    "Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6": 7,
    "Inborn_genetic_diseases|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4": 1,
    "Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|not_provided|GDF6-related_disorder|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_17": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|not_provided": 2,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Multiple_synostoses_syndrome_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|GDF6-related_disorder|not_provided": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Inborn_genetic_diseases": 2,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Inborn_genetic_diseases": 2,
    "Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Multiple_synostoses_syndrome_4|Leber_congenital_amaurosis_17|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|not_specified": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6": 8,
    "not_provided|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 2,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Multiple_synostoses_syndrome_4|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|GDF6-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract|Retinal_dystrophy|not_specified|not_provided|Klippel-Feil_syndrome": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4": 1,
    "Inborn_genetic_diseases|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4": 1,
    "Inborn_genetic_diseases|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 2,
    "Retinal_dystrophy|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|not_provided": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant": 1,
    "not_provided|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|not_specified": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6": 1,
    "Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Multiple_synostoses_syndrome_4|Leber_congenital_amaurosis_17|Inborn_genetic_diseases": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|not_specified": 1,
    "Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Inborn_genetic_diseases": 1,
    "not_provided|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6": 2,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Multiple_synostoses_syndrome_4|not_specified": 1,
    "Isolated_microphthalmia_4|Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Inborn_genetic_diseases": 1,
    "Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_17|Klippel-Feil_syndrome_1|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4|Inborn_genetic_diseases": 1,
    "Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|not_provided|GDF6-related_disorder": 1,
    "Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Microphthalmia|_isolated|_with_coloboma_6|not_provided|GDF6-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "GDF6-related_disorder|Klippel-Feil_syndrome_1|_autosomal_dominant|Leber_congenital_amaurosis_17|Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_4": 1,
    "Microphthalmia|_isolated|_with_coloboma_6|Leber_congenital_amaurosis_17|Isolated_microphthalmia_4|Klippel-Feil_syndrome_1|_autosomal_dominant|not_provided": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_3|not_provided": 2,
    "not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_3": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_3|not_provided|UQCRB-related_disorder": 1,
    "UQCRB-related_disorder|Mitochondrial_complex_III_deficiency_nuclear_type_3|not_provided": 1,
    "not_provided|UQCRB-related_disorder": 1,
    "UQCRB-related_disorder": 1,
    "not_provided|PTDSS1-related_disorder": 2,
    "Lenz-Majewski_hyperostosis_syndrome": 11,
    "not_provided|Lenz-Majewski_hyperostosis_syndrome|Inborn_genetic_diseases": 2,
    "Lenz-Majewski_hyperostosis_syndrome|not_provided": 4,
    "PTDSS1-related_disorder|not_provided": 2,
    "PTDSS1-related_disorder": 3,
    "Inborn_genetic_diseases|PTDSS1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|POP1-related_disorder": 1,
    "POP1-related_disorder|not_provided": 7,
    "Anauxetic_dysplasia_2": 7,
    "not_provided|Inborn_genetic_diseases|Anauxetic_dysplasia_2": 1,
    "not_provided|Anauxetic_dysplasia_2|Inborn_genetic_diseases": 1,
    "Anauxetic_dysplasia_2|not_provided": 2,
    "not_provided|POP1-related_disorder": 2,
    "Cohen_syndrome": 4372,
    "Cohen_syndrome|Abnormal_brain_morphology|not_specified": 1,
    "not_provided|Cohen_syndrome": 94,
    "Cohen_syndrome|not_specified|VPS13B-related_disorder": 8,
    "VPS13B-related_disorder|Cohen_syndrome": 194,
    "VPS13B-related_disorder": 199,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_provided|Cohen_syndrome|Intellectual_disability": 2,
    "VPS13B-related_disorder|not_provided|Cohen_syndrome": 17,
    "Cohen_syndrome|Inborn_genetic_diseases": 75,
    "Cohen_syndrome|not_specified": 11,
    "Cohen_syndrome|VPS13B-related_disorder": 179,
    "Inborn_genetic_diseases|Cohen_syndrome": 101,
    "Cohen_syndrome|not_provided": 82,
    "not_provided|VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome": 4,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Cohen_syndrome": 12,
    "Inborn_genetic_diseases|not_specified|Cohen_syndrome|VPS13B-related_disorder": 2,
    "Cohen_syndrome|VPS13B-related_disorder|Inborn_genetic_diseases": 27,
    "Abnormal_brain_morphology|Cohen_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Cohen_syndrome": 14,
    "VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome": 31,
    "VPS13B-related_disorder|Cohen_syndrome|Inborn_genetic_diseases": 21,
    "Cohen_syndrome|Inborn_genetic_diseases|VPS13B-related_disorder": 12,
    "Inborn_genetic_diseases|not_provided|VPS13B-related_disorder|Cohen_syndrome": 2,
    "not_provided|Cohen_syndrome|VPS13B-related_disorder": 13,
    "VPS13B-related_disorder|Cohen_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_specified|Cohen_syndrome|not_provided": 1,
    "not_specified|VPS13B-related_disorder|Cohen_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Cohen_syndrome|not_provided": 9,
    "Cohen_syndrome|not_provided|Inborn_genetic_diseases|VPS13B-related_disorder": 3,
    "Inborn_genetic_diseases|VPS13B-related_disorder|Cohen_syndrome|not_provided": 2,
    "Cohen_syndrome|Retinitis_pigmentosa": 1,
    "Cohen_syndrome|not_specified|VPS13B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "VPS13B-related_disorder|not_specified|Inborn_genetic_diseases|Cohen_syndrome": 2,
    "VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|VPS13B-related_disorder|Cohen_syndrome": 21,
    "Cohen_syndrome|VPS13B-related_disorder|not_provided": 16,
    "not_specified|Cohen_syndrome|not_provided": 6,
    "not_provided|Cohen_syndrome|Microcephaly|Hypotonia|Generalized_joint_hypermobility|Unsteady_gait|Carious_teeth|Global_developmental_delay|Intellectual_disability|Attention_deficit_hyperactivity_disorder": 1,
    "Inborn_genetic_diseases|not_specified|VPS13B-related_disorder": 1,
    "Inborn_genetic_diseases|VPS13B-related_disorder|not_specified|not_provided|Cohen_syndrome": 13,
    "Cohen_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "VPS13B-related_disorder|Cohen_syndrome|not_specified": 3,
    "not_provided|VPS13B-related_disorder|Cohen_syndrome": 9,
    "Cohen_syndrome|not_provided|VPS13B-related_disorder": 10,
    "VPS13B-related_disorder|Cohen_syndrome|not_provided": 12,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_provided|Cohen_syndrome": 16,
    "VPS13B-related_disorder|Cohen_syndrome|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Cohen_syndrome": 8,
    "not_specified|Cohen_syndrome": 16,
    "Cohen_syndrome|Intellectual_disability|VPS13B-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|VPS13B-related_disorder|Cohen_syndrome": 3,
    "Inborn_genetic_diseases|VPS13B-related_disorder|not_provided|not_specified|Cohen_syndrome": 2,
    "Inborn_genetic_diseases|VPS13B-related_disorder|Cohen_syndrome|not_specified": 1,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Cohen_syndrome|Intellectual_disability": 1,
    "not_provided|Cohen_syndrome|Inborn_genetic_diseases": 9,
    "Cohen_syndrome|not_specified|Inborn_genetic_diseases": 3,
    "Microcephaly|Cohen_syndrome": 2,
    "Cohen_syndrome|VPS13B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Cohen_syndrome|VPS13B-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Cohen_syndrome|VPS13B-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Cohen_syndrome": 5,
    "not_provided|Cohen_syndrome|Inborn_genetic_diseases|VPS13B-related_disorder": 2,
    "VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|VPS13B-related_disorder|Cohen_syndrome": 1,
    "not_provided|not_specified|Cohen_syndrome|Inborn_genetic_diseases": 3,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_provided|Cohen_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Cohen_syndrome": 16,
    "Cohen_syndrome|Abnormality_of_the_eye|not_provided": 1,
    "VPS13B-related_disorder|Cohen_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Cohen_syndrome|VPS13B-related_disorder": 14,
    "not_provided|Inborn_genetic_diseases|VPS13B-related_disorder|not_specified|Cohen_syndrome|Intellectual_disability": 1,
    "VPS13B-related_disorder|not_provided|Cohen_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|VPS13B-related_disorder|Cohen_syndrome": 4,
    "Inborn_genetic_diseases|VPS13B-related_disorder|not_provided|Cohen_syndrome": 6,
    "Cohen_syndrome|VPS13B-related_disorder|Intellectual_disability": 1,
    "not_specified|VPS13B-related_disorder|not_provided|Cohen_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|VPS13B-related_disorder": 8,
    "Inborn_genetic_diseases|not_provided|Cohen_syndrome|VPS13B-related_disorder": 2,
    "Cohen_syndrome|VPS13B-related_disorder|not_specified": 1,
    "Cohen_syndrome|not_provided|Inborn_genetic_diseases": 7,
    "Cohen_syndrome|not_provided|VPS13B-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|Cohen_syndrome|Abnormality_of_the_eye": 2,
    "not_specified|Cohen_syndrome|Inborn_genetic_diseases|not_provided|VPS13B-related_disorder": 1,
    "not_provided|Cohen_syndrome|not_specified": 2,
    "VPS13B-related_disorder|Cohen_syndrome|not_provided|not_specified": 1,
    "Cohen_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Cohen_syndrome|not_provided|VPS13B-related_disorder": 1,
    "Cohen_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "VPS13B-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Cohen_syndrome|not_specified": 1,
    "Cohen_syndrome|Pituitary_stalk_interruption_syndrome|VPS13B-related_disorder": 1,
    "Cohen_syndrome|VPS13B-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Cohen_syndrome|VPS13B-related_disorder|Inborn_genetic_diseases": 6,
    "Microcephaly|Small_hand|Progressive_visual_loss|Short_stature|Retinal_dystrophy|Intellectual_disability|Recurrent_aphthous_stomatitis|Short_foot|Decreased_total_neutrophil_count|Cohen_syndrome": 1,
    "Cohen_syndrome|not_provided|not_specified": 2,
    "Myopia|Intellectual_disability|Retinal_dystrophy|Joint_laxity|Mild_hearing_impairment|Optic_disc_pallor|High_myopia|Global_developmental_delay|Cohen_syndrome": 1,
    "Cohen_syndrome|not_specified|VPS13B-related_disorder|not_provided": 1,
    "VPS13B-related_disorder|not_provided|Cohen_syndrome|Inborn_genetic_diseases": 3,
    "Cohen_syndrome|not_specified|not_provided|VPS13B-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|VPS13B-related_disorder|Cohen_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Cohen_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cohen_syndrome|not_specified|VPS13B-related_disorder": 1,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cohen_syndrome": 1,
    "Cohen_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|VPS13B-related_disorder|Cohen_syndrome": 1,
    "Cohen_syndrome|not_provided|Abnormality_of_the_nervous_system": 1,
    "Abnormality_of_the_nervous_system|not_provided|Cohen_syndrome": 1,
    "Inborn_genetic_diseases|Cohen_syndrome|not_specified|not_provided": 1,
    "VPS13B-related_disorder|Cohen_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "VPS13B-related_disorder|Cohen_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "VPS13B-related_disorder|not_specified|Cohen_syndrome": 1,
    "Inborn_genetic_diseases|Cohen_syndrome|not_provided|not_specified": 2,
    "VPS13B-related_disorder|not_provided": 4,
    "not_provided|VPS13B-related_disorder|Cohen_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Retinitis_pigmentosa|Cohen_syndrome": 1,
    "Cohen_syndrome|not_provided|not_specified|VPS13B-related_disorder": 1,
    "Cohen_syndrome|Inborn_genetic_diseases|not_provided|VPS13B-related_disorder": 1,
    "not_provided|not_specified|VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome": 1,
    "not_specified|VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome": 1,
    "not_provided|VPS13B-related_disorder|Inborn_genetic_diseases|not_specified|Cohen_syndrome": 1,
    "Cohen_syndrome|not_specified|not_provided|VPS13B-related_disorder": 2,
    "not_specified|not_provided|Cohen_syndrome|VPS13B-related_disorder": 1,
    "not_specified|VPS13B-related_disorder|not_provided|Cohen_syndrome": 1,
    "Inborn_genetic_diseases|Cohen_syndrome|VPS13B-related_disorder|not_provided": 1,
    "not_provided|not_specified|Cohen_syndrome": 2,
    "Cohen_syndrome|Inborn_genetic_diseases|VPS13B-related_disorder|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Cohen_syndrome": 1,
    "Cohen_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Cohen_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|VPS13B-related_disorder|not_specified|Cohen_syndrome": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Cohen_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Cohen_syndrome|VPS13B-related_disorder|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|Cohen_syndrome": 1,
    "VPS13B-related_disorder|Inborn_genetic_diseases|not_specified|Cohen_syndrome": 1,
    "VPS13B-related_disorder|Inborn_genetic_diseases|Cohen_syndrome|not_specified|not_provided": 1,
    "VPS13B-related_disorder|not_specified|not_provided|Cohen_syndrome": 3,
    "VPS13B-related_disorder|not_specified|Cohen_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Cohen_syndrome": 1,
    "Cohen_syndrome|not_specified|VPS13B-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|VPS13B-related_disorder": 1,
    "Cohen_syndrome|Inborn_genetic_diseases|not_specified|VPS13B-related_disorder": 1,
    "Inborn_genetic_diseases|VPS13B-related_disorder|not_specified|not_provided|Cohen_syndrome|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|VPS13B-related_disorder|Cohen_syndrome": 1,
    "Inborn_genetic_diseases|Cohen_syndrome|VPS13B-related_disorder|not_provided|not_specified": 1,
    "not_specified|Cohen_syndrome|Inborn_genetic_diseases": 1,
    "Cohen_syndrome|See_cases": 1,
    "Cohen_syndrome|Small_hand|Recurrent_aphthous_stomatitis|Short_foot|Decreased_total_neutrophil_count|Progressive_visual_loss|Short_stature|Retinal_dystrophy|Intellectual_disability|Microcephaly|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|VPS13B-related_disorder|Cohen_syndrome": 1,
    "not_provided|Cohen_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Myopia|Intellectual_disability|Retinal_dystrophy|Joint_laxity|Mild_hearing_impairment|Optic_disc_pallor|High_myopia|Global_developmental_delay": 1,
    "not_provided|Cohen_syndrome|Abnormality_of_the_nervous_system": 1,
    "Spermatogenic_failure_64": 1,
    "Spermatogenic_failure_64|Oocyte_maturation_defect_12": 1,
    "Oocyte_maturation_defect_12": 2,
    "Primary_ciliary_dyskinesia_28": 273,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_28": 34,
    "Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia": 35,
    "Primary_ciliary_dyskinesia|SPAG1-related_disorder|Primary_ciliary_dyskinesia_28": 2,
    "VPS13B-related_disorder|Primary_ciliary_dyskinesia_28|not_provided": 1,
    "Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia|SPAG1-related_disorder": 3,
    "SPAG1-related_disorder|Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia": 1,
    "SPAG1-related_disorder|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_28": 1,
    "not_provided|Primary_ciliary_dyskinesia_28": 6,
    "Primary_ciliary_dyskinesia_28|SPAG1-related_disorder": 5,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_28|SPAG1-related_disorder": 4,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_28": 2,
    "not_provided|Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_28|not_provided|Primary_ciliary_dyskinesia": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 10,
    "SPAG1-related_disorder": 3,
    "Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_28": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_28": 2,
    "Primary_ciliary_dyskinesia_28|not_specified|not_provided|Primary_ciliary_dyskinesia": 3,
    "Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia|not_specified|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia_28|not_specified": 1,
    "Primary_ciliary_dyskinesia_28|SPAG1-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_28|VPS13B-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_28|not_provided": 5,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_28|not_provided": 1,
    "SPAG1-related_disorder|not_provided|Primary_ciliary_dyskinesia_28|Primary_ciliary_dyskinesia": 1,
    "SPAG1-related_disorder|Primary_ciliary_dyskinesia_28": 1,
    "Primary_ciliary_dyskinesia_28|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "VPS13B-related_disorder|Primary_ciliary_dyskinesia_28": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Primary_ciliary_dyskinesia_28": 1,
    "not_specified|Primary_ciliary_dyskinesia|SPAG1-related_disorder|Primary_ciliary_dyskinesia_28": 1,
    "not_specified|Primary_ciliary_dyskinesia_28|not_provided|Primary_ciliary_dyskinesia": 1,
    "PABPC1-related_condition": 2,
    "not_provided|See_cases|POPOV-CHANG_SYNDROME|Noonan-like_disorder|YWHAZ-related_neurodevelopmental_syndrome|not_specified": 1,
    "POPOV-CHANG_SYNDROME": 4,
    "YWHAZ-related_disorder|not_provided": 1,
    "Cardiofaciocutaneous_spectrum_disorder": 1,
    "not_provided|YWHAZ-related_disorder": 1,
    "not_specified|POPOV-CHANG_SYNDROME": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_28|Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome|not_provided|Corneal_dystrophy|_posterior_polymorphous|_4": 1,
    "Corneal_dystrophy|_posterior_polymorphous|_4|Corneal_dystrophy": 2,
    "GRHL2-related_disorder": 4,
    "not_provided|GRHL2-related_disorder": 4,
    "GRHL2-related_disorder|not_specified|not_provided": 3,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_28|Corneal_dystrophy|_posterior_polymorphous|_4|Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_28": 6,
    "not_specified|not_provided|Corneal_dystrophy|_posterior_polymorphous|_4": 1,
    "GRHL2-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_28|not_specified|not_provided": 1,
    "Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_28|Corneal_dystrophy|_posterior_polymorphous|_4|not_specified|not_provided": 1,
    "Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome|not_provided": 1,
    "Corneal_dystrophy|_posterior_polymorphous|_4": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Corneal_dystrophy|_posterior_polymorphous|_4": 1,
    "Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_28|Corneal_dystrophy|_posterior_polymorphous|_4|Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_28|Corneal_dystrophy|_posterior_polymorphous|_4|not_specified|not_provided|Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome": 1,
    "not_provided|Corneal_dystrophy|_posterior_polymorphous|_4|Autosomal_dominant_nonsyndromic_hearing_loss_28|Nail_and_teeth_abnormalities-marginal_palmoplantar_keratoderma-oral_hyperpigmentation_syndrome": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a": 13,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a": 28,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_provided|Mitochondrial_DNA_depletion_syndrome_8a": 3,
    "Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 20,
    "Mitochondrial_DNA_depletion_syndrome|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions": 3,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Mitochondrial_DNA_depletion_syndrome": 3,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 4,
    "Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|not_provided": 6,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|not_specified": 1,
    "RRM2B-related_mitochondrial_disease": 9,
    "not_provided|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 2,
    "Mitochondrial_DNA_depletion_syndrome_8a": 15,
    "RRM2B-related_mitochondrial_disease|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_mitochondrial_disease": 1,
    "RRM2B-related_disorder|not_provided": 4,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_mitochondrial_disease|Mitochondrial_disease": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 10,
    "RRM2B-related_mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome_8a": 3,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_mitochondrial_disease|not_provided": 3,
    "RRM2B-related_mitochondrial_disease|Progressive_external_ophthalmoplegia|not_provided": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_specified|not_provided": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Sensorineural_hearing_loss_disorder|Adult_Fanconi_syndrome|Rod-cone_dystrophy|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 3,
    "RRM2B-related_disorder": 5,
    "RRM2B-related_mitochondrial_disease|not_provided|Mitochondrial_DNA_depletion_syndrome_8a": 1,
    "not_specified|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Severe_lactic_acidosis": 1,
    "RRM2B-related_mitochondrial_disease|not_provided": 4,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Inborn_genetic_diseases": 1,
    "RRM2B-related_mitochondrial_disease|Progressive_external_ophthalmoplegia": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|not_provided": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_8a|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|RRM2B-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction": 1,
    "Mitochondrial_DNA_depletion_syndrome_8a|not_provided": 4,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|not_provided": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Mitochondrial_DNA_depletion_syndrome_8a|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_mitochondrial_disease|not_specified": 1,
    "RRM2B-related_mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome_8B_(MNGIE_type)": 1,
    "RRM2B-related_mitochondrial_disease|not_provided|Mitochondrial_DNA_depletion_syndrome_8B_(MNGIE_type)|Mitochondrial_DNA_depletion_syndrome_8a": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|RRM2B-related_mitochondrial_disease": 1,
    "Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Inborn_genetic_diseases|not_provided": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Idiopathic_camptocormia|RRM2B-related_mitochondrial_disease|not_provided": 1,
    "not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_provided|Mitochondrial_DNA_depletion_syndrome_8a": 1,
    "RRM2B-related_disorder|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5": 1,
    "RRM2B-related_mitochondrial_disease|not_specified|not_provided": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_mitochondrial_disease": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_provided": 2,
    "not_provided|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_disorder": 1,
    "RRM2B-related_mitochondrial_disease|not_provided|Progressive_external_ophthalmoplegia|Mitochondrial_DNA_depletion_syndrome_8a": 1,
    "Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|not_provided|RRM2B-related_disorder": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|not_specified|not_provided": 1,
    "not_provided|RRM2B-related_disorder": 2,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_provided": 1,
    "RRM2B-related_disorder|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_specified|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|RRM2B-related_disorder": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|RRM2B-related_mitochondrial_disease|Mitochondrial_disease|not_provided": 1,
    "Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Mitochondrial_DNA_depletion_syndrome_8a|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_8a|Rod-cone_dystrophy|_sensorineural_deafness|_and_Fanconi-type_renal_dysfunction|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_5|not_provided": 2,
    "UBR5-related_disorder": 27,
    "not_provided|UBR5-related_disorder": 3,
    "UBR5-related_disorder|not_provided": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_SPEECH_DELAY_AND_BEHAVIORAL_ABNORMALITIES": 5,
    "not_specified|UBR5-related_disorder": 1,
    "UBR5-associated_neurodevelopmental_condition|UBR5-related_disorder": 1,
    "UBR5-related_neurodevelopmental_disorder": 1,
    "UBR5-related_disorder|not_specified": 1,
    "not_provided|NEURODEVELOPMENTAL_DISORDER_WITH_SPEECH_DELAY_AND_BEHAVIORAL_ABNORMALITIES": 1,
    "UBR5-associated_neurodevelopmental_disorder": 1,
    "KLF10-related_disorder|not_provided": 1,
    "KLF10-related_disorder|not_specified": 1,
    "not_provided|KLF10-related_disorder": 2,
    "KLF10-related_disorder": 1,
    "DOORS_syndrome": 6,
    "FZD6-related_disorder": 8,
    "not_provided|Nonsyndromic_congenital_nail_disorder_1": 2,
    "Nephroblastoma|not_provided": 1,
    "Non-immune_hydrops_fetalis|Nonsyndromic_congenital_nail_disorder_1": 1,
    "Nonsyndromic_congenital_nail_disorder_1|not_provided": 1,
    "Nonsyndromic_congenital_nail_disorder_1": 4,
    "Nonsyndromic_congenital_nail_disorder_1|Nail_disease": 2,
    "SLC25A32-related_disorder|not_provided": 3,
    "not_provided|SLC25A32-related_disorder|Exercise_intolerance|_riboflavin-responsive": 1,
    "not_provided|SLC25A32-related_disorder": 3,
    "not_provided|SLC25A32-related_disorder|not_specified": 1,
    "not_specified|Exercise_intolerance|_riboflavin-responsive|not_provided": 1,
    "Exercise_intolerance|_riboflavin-responsive|not_provided|not_specified": 1,
    "SLC25A32-related_disorder": 1,
    "Cone-rod_synaptic_disorder_syndrome|_congenital_nonprogressive": 7,
    "RIMS2-related_disorder": 2,
    "Cone-rod_synaptic_disorder_syndrome|_congenital_nonprogressive|not_provided": 2,
    "Cone-rod_synaptic_disorder|_congenital_nonprogressive|not_provided": 8,
    "Cone-rod_synaptic_disorder|_congenital_nonprogressive": 71,
    "Dihydropyrimidinase_deficiency": 30,
    "Dihydropyrimidinase_deficiency|not_provided": 12,
    "Dihydropyrimidinase_deficiency|not_provided|See_cases|not_specified": 1,
    "Dihydropyrimidinase_deficiency|DPYS-related_disorder|not_provided": 2,
    "not_provided|Dihydropyrimidinase_deficiency": 16,
    "Inborn_genetic_diseases|not_provided|Dihydropyrimidinase_deficiency": 2,
    "Dihydropyrimidinase_deficiency|not_provided|not_specified": 1,
    "DPYS-related_disorder|not_provided": 2,
    "not_provided|DPYS-related_disorder": 1,
    "Dihydropyrimidinase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|DPYS-related_disorder": 1,
    "DPYS-related_disorder|not_provided|Dihydropyrimidinase_deficiency": 1,
    "not_provided|Dihydropyrimidinase_deficiency|DPYS-related_disorder": 1,
    "Oculopharyngodistal_myopathy_1|Amyotrophic_lateral_sclerosis_28|not_provided": 1,
    "LRP12-related_disorder": 1,
    "Oculopharyngodistal_myopathy_1|Amyotrophic_lateral_sclerosis_28": 1,
    "not_provided|LRP12-related_disorder": 1,
    "ZFPM2-related_disorder": 11,
    "46|XY_sex_reversal_9": 149,
    "46|XY_sex_reversal_9|Diaphragmatic_hernia_3|Tetralogy_of_Fallot": 1,
    "46|XY_sex_reversal_9|not_provided": 7,
    "ZFPM2-related_disorder|46|XY_sex_reversal_9|not_specified|not_provided|Double_outlet_right_ventricle|Tetralogy_of_Fallot|Diaphragmatic_hernia_3|46|XY_sex_reversal_3": 1,
    "46|XY_sex_reversal_9|Inborn_genetic_diseases|not_provided": 2,
    "46|XY_sex_reversal_9|not_provided|Diaphragmatic_hernia_3": 1,
    "Diaphragmatic_hernia_3|Tetralogy_of_Fallot|46|XY_sex_reversal_9": 3,
    "Inborn_genetic_diseases|ZFPM2-related_disorder": 2,
    "ZFPM2-related_disorder|46|XY_sex_reversal_9": 3,
    "46|XY_sex_reversal_9|not_specified": 3,
    "ZFPM2-related_disorder|Inborn_genetic_diseases|46|XY_sex_reversal_9": 1,
    "not_provided|46|XY_sex_reversal_9": 4,
    "46|XY_sex_reversal_9|Inborn_genetic_diseases": 12,
    "46|XY_sex_reversal_3|not_provided|46|XY_sex_reversal_9|ZFPM2-related_disorder": 1,
    "not_provided|not_specified|Tetralogy_of_Fallot|46|XY_sex_reversal_9": 1,
    "Inborn_genetic_diseases|46|XY_sex_reversal_9": 9,
    "not_provided|Diaphragmatic_hernia_3": 1,
    "Diaphragmatic_hernia_3": 7,
    "Tetralogy_of_Fallot|Diaphragmatic_hernia_3|46|XY_sex_reversal_9|Inborn_genetic_diseases": 1,
    "46|XY_sex_reversal_9|not_specified|not_provided|46|XY_sex_reversal_3": 1,
    "not_provided|ZFPM2-related_disorder|46|XY_sex_reversal_9": 1,
    "Double_outlet_right_ventricle": 2,
    "Diaphragmatic_hernia_3|not_provided": 1,
    "46|XY_sex_reversal_9|46|XY_sex_reversal_3": 2,
    "not_specified|46|XY_sex_reversal_9": 2,
    "46|XY_sex_reversal_9|ZFPM2-related_disorder": 2,
    "46|XY_sex_reversal_9|Inborn_genetic_diseases|not_specified": 1,
    "46|XY_sex_reversal_9|Diaphragmatic_hernia_3": 1,
    "not_provided|not_specified|46|XY_sex_reversal_9": 3,
    "not_specified|46|XY_sex_reversal_9|not_provided": 1,
    "Tetralogy_of_Fallot|46|XY_sex_reversal_9": 1,
    "Inborn_genetic_diseases|46|XY_sex_reversal_9|not_provided": 1,
    "not_specified|not_provided|46|XY_sex_reversal_9": 4,
    "46|XY_sex_reversal_9|Inborn_genetic_diseases|Diaphragmatic_hernia_3|Tetralogy_of_Fallot": 1,
    "46|XY_sex_reversal_9|46|XY_sex_reversal_3|not_provided": 1,
    "46|XY_sex_reversal_3|not_provided|ZFPM2-related_disorder|Tetralogy_of_Fallot|not_specified|Diaphragmatic_hernia_3|46|XY_sex_reversal_9": 1,
    "not_provided|46|XY_sex_reversal_9|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|46|XY_sex_reversal_9": 1,
    "Tetralogy_of_Fallot|46|XY_sex_reversal_9|not_specified|Diaphragmatic_hernia_3|not_provided": 1,
    "Diaphragmatic_hernia_3|46|XY_sex_reversal_3|46|XY_sex_reversal_9|Double_outlet_right_ventricle|ZFPM2-related_disorder|not_provided|Tetralogy_of_Fallot|not_specified": 1,
    "46|XY_sex_reversal_9|not_specified|not_provided": 2,
    "ZFPM2-related_disorder|not_specified|46|XY_sex_reversal_9|not_provided": 1,
    "46|XY_sex_reversal_9|ZFPM2-related_disorder|not_specified": 1,
    "46|XY_sex_reversal_9|not_provided|not_specified": 2,
    "Diaphragmatic_hernia_3|46|XY_sex_reversal_9": 1,
    "ZFPM2-related_disorder|Inborn_genetic_diseases": 1,
    "ZFPM2-related_disorder|46|XY_sex_reversal_9|Diaphragmatic_hernia_3|Tetralogy_of_Fallot": 1,
    "OXR1-related_disorder": 2,
    "Congenital_cerebellar_hypoplasia|Inborn_genetic_diseases": 1,
    "OXR1-related_disorder|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "Congenital_cerebellar_hypoplasia|not_provided": 4,
    "ANGPT1-related_disorder|not_provided|Agammaglobulinemia_7|_autosomal_recessive|Hereditary_angioedema_type_3": 1,
    "ANGPT1-related_disorder": 4,
    "Angioedema|_hereditary|_5|not_provided": 1,
    "ANGPT1-related_disorder|not_provided": 1,
    "not_provided|RSPO2-related_disorder": 1,
    "Tetraamelia-multiple_malformations_syndrome": 2,
    "not_provided|Tetraamelia_syndrome_2|Humerofemoral_hypoplasia_with_radiotibial_ray_deficiency": 1,
    "Tetraamelia_syndrome_2|Humerofemoral_hypoplasia_with_radiotibial_ray_deficiency|not_provided": 1,
    "RSPO2-related_disorder|not_provided": 1,
    "Tetraamelia_syndrome_2": 2,
    "Humerofemoral_hypoplasia_with_radiotibial_ray_deficiency": 1,
    "RSPO2-related_disorder": 2,
    "TRHR-related_disorder": 2,
    "Hypothyroidism|_congenital|_nongoitrous|_7": 6,
    "not_provided|TRHR-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_124": 6,
    "PKHD1L1-related_disorder": 17,
    "PKHD1L1-related_disorder|not_specified": 2,
    "PKHD1L1-related_disorder|not_provided": 1,
    "CSMD3-related_disorder": 54,
    "Familial_meningioma|CSMD3-related_disorder": 1,
    "not_provided|CSMD3-related_disorder": 13,
    "CSMD3-related_disorder|not_provided": 12,
    "Familial_meningioma|not_specified": 6,
    "not_specified|CSMD3-associated_Hirschsprung_disease": 1,
    "Pachygyria-intellectual_disability-epilepsy_syndrome": 2,
    "Trichorhinophalangeal_syndrome": 17,
    "not_provided|Trichorhinophalangeal_syndrome": 2,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|not_provided": 6,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 192,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 176,
    "Inborn_genetic_diseases|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 13,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 8,
    "Trichorhinophalangeal_dysplasia_type_I": 57,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|Inborn_genetic_diseases": 13,
    "Inborn_genetic_diseases|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 14,
    "TRPS1-related_disorder|Inborn_genetic_diseases": 1,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_specified": 2,
    "TRPS1-related_disorder|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 2,
    "TRPS1-related_disorder": 7,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|Inborn_genetic_diseases|TRPS1-related_disorder": 1,
    "Trichorhinophalangeal_syndrome|_type_III": 3,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|Inborn_genetic_diseases": 4,
    "TRPS1-related_disorder|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "TRPS1-related_disorder|not_provided|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "not_provided|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 10,
    "TRPS1-related_disorder|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 1,
    "not_provided|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 3,
    "not_specified|not_provided|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 1,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|Alopecia_areata|Proportionate_short_stature|Brachydactyly|Pear-shaped_nose": 1,
    "Trichorhinophalangeal_dysplasia_type_I|not_provided": 2,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|Metaphyseal_chondrodysplasia": 1,
    "Langer-Giedion_syndrome|not_provided": 1,
    "Trichorhinophalangeal_syndrome_type_I_or_III": 2,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_syndrome": 1,
    "not_provided|not_specified|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "not_provided|not_specified|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 1,
    "Inborn_genetic_diseases|Microcephaly": 1,
    "TRPS1-related_disorder|not_provided|Trichorhinophalangeal_dysplasia_type_I": 1,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|not_provided|Inborn_genetic_diseases": 2,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|Inborn_genetic_diseases|not_specified": 1,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "Langer-Giedion_syndrome|TRPS1-related_disorder|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 1,
    "TRPS1-related_disorder|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|Inborn_genetic_diseases": 1,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|TRPS1-related_disorder": 1,
    "Hyperextensible_skin|Sparse_and_thin_eyebrow|Short_stature|Craniosynostosis_syndrome|Sparse_hair|Abnormally_high-pitched_voice|Mitral_valve_prolapse": 1,
    "not_specified|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 1,
    "not_specified|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided|TRPS1-related_disorder": 1,
    "not_provided|TRPS1-related_disorder|Inborn_genetic_diseases|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "not_provided|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|not_specified": 1,
    "See_cases|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III": 1,
    "Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|TRPS1-related_disorder": 1,
    "Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 1,
    "TRPS1-related_disorder|Inborn_genetic_diseases|Trichorhinophalangeal_dysplasia_type_I|Trichorhinophalangeal_syndrome|_type_III|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Trichorhinophalangeal_syndrome|_type_III|Trichorhinophalangeal_dysplasia_type_I": 1,
    "not_provided|not_specified|Trichorhinophalangeal_dysplasia_type_I": 1,
    "Trichorhinophalangeal_syndrome|not_provided": 2,
    "Cornelia_de_Lange_syndrome_4|not_specified": 2,
    "Cornelia_de_Lange_syndrome_4": 177,
    "Cornelia_de_Lange_syndrome_4|not_provided": 6,
    "Mungan_syndrome": 1,
    "not_provided|Cornelia_de_Lange_syndrome_4": 11,
    "RAD21-related_disorder": 9,
    "Cornelia_de_Lange_syndrome_4|Inborn_genetic_diseases": 17,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_4": 15,
    "Cornelia_de_Lange_syndrome_4|See_cases": 1,
    "Intellectual_disability|Cone-rod_dystrophy": 1,
    "not_specified|Cornelia_de_Lange_syndrome_4": 1,
    "Inborn_genetic_diseases|not_provided|Cornelia_de_Lange_syndrome_4": 1,
    "Cornelia_de_Lange_syndrome_4|not_provided|RAD21-related_disorder|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_4|RAD21-related_disorder|Inborn_genetic_diseases": 2,
    "Mungan_syndrome|Cornelia_de_Lange_syndrome_4": 1,
    "Cornelia_de_Lange_syndrome_4|not_specified|not_provided|Mungan_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_4": 1,
    "Mungan_syndrome|Cornelia_de_Lange_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Cornelia_de_Lange_syndrome_4|Inborn_genetic_diseases": 3,
    "Cornelia_de_Lange_syndrome_4|RAD21-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Cornelia_de_Lange_syndrome_4": 2,
    "RAD21-related_disorder|not_provided|Cornelia_de_Lange_syndrome_4": 1,
    "RAD21-related_disorder|Cornelia_de_Lange_syndrome_4": 3,
    "Cornelia_de_Lange_syndrome_4|not_provided|not_specified": 1,
    "not_provided|Cornelia_de_Lange_syndrome_4|Hereditary_cancer-predisposing_syndrome|Mungan_syndrome": 1,
    "Cornelia_de_Lange_syndrome_4|Intellectual_disability": 1,
    "not_provided|Mungan_syndrome|Cornelia_de_Lange_syndrome_4": 3,
    "not_provided|Cornelia_de_Lange_syndrome_4|Mungan_syndrome": 1,
    "not_provided|not_specified|Cornelia_de_Lange_syndrome_4|Mungan_syndrome": 2,
    "RAD21-related_disorder|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_4|Inborn_genetic_diseases|not_provided|RAD21-related_disorder": 1,
    "Cornelia_de_Lange_syndrome_4|Mungan_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|RAD21-related_disorder|not_provided": 1,
    "SLC30A8-related_disorder": 4,
    "SLC30A8-related_disorder|Diabetes_mellitus_type_2|_susceptibility_to": 1,
    "Exostoses|_multiple|_type_1": 37,
    "Multiple_congenital_exostosis": 693,
    "EXT1-related_disorder|Multiple_congenital_exostosis": 7,
    "Multiple_congenital_exostosis|not_provided": 28,
    "not_provided|Multiple_congenital_exostosis": 37,
    "Chondrosarcoma|Multiple_congenital_exostosis": 13,
    "Inborn_genetic_diseases|Multiple_congenital_exostosis": 7,
    "Multiple_congenital_exostosis|EXT1-related_disorder|not_provided": 2,
    "Chondrosarcoma": 49,
    "not_provided|EXT1-related_disorder|Exostoses|_multiple|_type_1|Multiple_congenital_exostosis": 1,
    "Exostoses|_multiple|_type_1|Multiple_congenital_exostosis": 11,
    "Chondrosarcoma|Exostoses|_multiple|_type_1": 3,
    "Multiple_congenital_exostosis|Exostoses|_multiple|_type_1|Chondrosarcoma": 2,
    "Inborn_genetic_diseases|Chondrosarcoma": 1,
    "EXT1-related_disorder|Exostoses|_multiple|_type_1|Multiple_congenital_exostosis|Ovarian_cancer": 1,
    "not_provided|Exostoses|_multiple|_type_1": 3,
    "Exostoses|_multiple|_type_1|Chondrosarcoma": 8,
    "Multiple_congenital_exostosis|Chondrosarcoma|Inborn_genetic_diseases": 3,
    "not_provided|Exostoses|_multiple|_type_1|Multiple_congenital_exostosis": 1,
    "EXT1-related_disorder": 14,
    "not_provided|EXT1-related_disorder": 1,
    "Chondrosarcoma|Exostoses|_multiple|_type_1|Multiple_congenital_exostosis": 4,
    "Multiple_congenital_exostosis|EXT1-related_disorder": 8,
    "Multiple_congenital_exostosis|Malignant_tumor_of_breast": 1,
    "Multiple_congenital_exostosis|Exostoses|_multiple|_type_1": 6,
    "not_specified|not_provided|Multiple_congenital_exostosis|Exostoses|_multiple|_type_1": 1,
    "Inborn_genetic_diseases|Multiple_congenital_exostosis|Chondrosarcoma": 1,
    "not_provided|not_specified|Multiple_congenital_exostosis|Exostoses|_multiple|_type_1": 1,
    "Multiple_congenital_exostosis|Exostoses": 1,
    "Exostoses|_multiple|_type_1|Multiple_congenital_exostosis|Chondrosarcoma": 2,
    "Multiple_congenital_exostosis|Ovarian_cancer": 1,
    "Multiple_congenital_exostosis|not_specified|not_provided|Exostoses|_multiple|_type_1": 1,
    "Multiple_congenital_exostosis|Inborn_genetic_diseases": 5,
    "Multiple_congenital_exostosis|Chondrosarcoma": 17,
    "Multiple_congenital_exostosis|not_specified|Exostoses|_multiple|_type_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_congenital_exostosis": 1,
    "Chondrosarcoma|Exostoses|_multiple|_type_1|Multiple_congenital_exostosis|not_provided": 1,
    "not_provided|Multiple_congenital_exostosis|Chondrosarcoma|Exostoses|_multiple|_type_1": 1,
    "not_provided|Chondrosarcoma|Exostoses|_multiple|_type_1|Multiple_congenital_exostosis": 1,
    "EXT1-related_disorder|Microcephaly|not_specified|Multiple_congenital_exostosis": 1,
    "Exostoses|_multiple|_type_1|Chondrosarcoma|Inborn_genetic_diseases": 1,
    "not_provided|Chondrosarcoma|Multiple_congenital_exostosis|Inborn_genetic_diseases": 1,
    "not_specified|Multiple_congenital_exostosis|Exostoses|_multiple|_type_1|not_provided": 1,
    "EXT1-related_disorder|not_specified|Multiple_congenital_exostosis|Chondrosarcoma|Exostoses|_multiple|_type_1": 1,
    "Multiple_congenital_exostosis|not_specified|not_provided|Exostoses|_multiple|_type_1|Langer-Giedion_syndrome": 1,
    "Ovarian_cancer|Multiple_congenital_exostosis": 1,
    "not_specified|Exostoses|_multiple|_type_1": 1,
    "Inborn_genetic_diseases|not_specified|Multiple_congenital_exostosis": 1,
    "Chondrosarcoma|Inborn_genetic_diseases|not_specified|Multiple_congenital_exostosis|not_provided": 1,
    "Exostoses|_multiple|_type_1|not_provided": 1,
    "Chondrosarcoma|Ovarian_cancer|Multiple_congenital_exostosis": 1,
    "Multiple_congenital_exostosis|Chondrosarcoma|not_specified": 1,
    "Childhood_neoplasm|EXT1-related_disorder|Exostoses|_multiple|_type_1|not_provided|Multiple_congenital_exostosis": 1,
    "Exostoses|_multiple|_type_1|not_provided|Multiple_congenital_exostosis|not_specified": 1,
    "Exostoses|_multiple|_type_1|Chondrosarcoma|Multiple_congenital_exostosis": 3,
    "Exostoses|_multiple|_type_1|EXT1-related_disorder|Multiple_congenital_exostosis|not_provided": 1,
    "not_provided|Multiple_congenital_exostosis|Exostoses|_multiple|_type_1|Chondrosarcoma|EXT1-related_disorder|Inborn_genetic_diseases": 1,
    "Multiple_congenital_exostosis|not_provided|Exostoses|_multiple|_type_1": 2,
    "Exostoses|_multiple|_type_1|not_provided|Multiple_congenital_exostosis": 1,
    "Multiple_congenital_exostosis|Chondrosarcoma|Exostoses|_multiple|_type_1": 2,
    "Multiple_congenital_exostosis|not_specified": 1,
    "not_provided|Hereditary_Multiple_Osteochondromatosis|Multiple_congenital_exostosis": 1,
    "not_specified|Multiple_congenital_exostosis": 1,
    "Ovarian_cancer|Multiple_congenital_exostosis|Exostoses|_multiple|_type_1": 1,
    "Multiple_congenital_exostosis|EXT1-related_disorder|Exostoses|_multiple|_type_1|not_provided": 1,
    "Chondrosarcoma|Exostoses|_multiple|_type_1|not_provided|Multiple_congenital_exostosis": 1,
    "Multiple_congenital_exostosis|not_provided|Chondrosarcoma": 1,
    "Multiple_congenital_exostosis|Hereditary_cancer": 1,
    "EXT1-related_disorder|Exostoses|_multiple|_type_1": 1,
    "Multiple_congenital_exostosis|Inborn_genetic_diseases|Chondrosarcoma": 1,
    "Chondrosarcoma|Inborn_genetic_diseases|Multiple_congenital_exostosis": 1,
    "Multiple_congenital_exostosis|Hereditary_Multiple_Osteochondromatosis": 1,
    "Chondrosarcoma|Inborn_genetic_diseases": 1,
    "Exostoses|_multiple|_type_1|Chondrosarcoma|Inborn_genetic_diseases|Multiple_congenital_exostosis": 1,
    "not_specified|Multiple_congenital_exostosis|Chondrosarcoma|Exostoses|_multiple|_type_1|not_provided": 1,
    "not_provided|Multiple_congenital_exostosis|Exostoses|_multiple|_type_1|not_specified": 2,
    "Chondrosarcoma|Ovarian_cancer": 1,
    "not_provided|Multiple_congenital_exostosis|EXT1-related_disorder": 1,
    "Multiple_congenital_exostosis|Exostoses|_multiple|_type_1|not_provided": 1,
    "Multiple_congenital_exostosis|Langer-Giedion_syndrome": 1,
    "Hereditary_Multiple_Osteochondromatosis": 2,
    "Hereditary_Multiple_Osteochondromatosis|not_provided": 1,
    "Epilepsy|_familial_adult_myoclonic|_1": 2,
    "Hyperphosphatasemia_with_bone_disease": 32,
    "Hyperphosphatasemia_with_bone_disease|not_provided": 4,
    "not_provided|Hyperphosphatasemia_with_bone_disease": 18,
    "not_provided|not_specified|Hyperphosphatasemia_with_bone_disease": 5,
    "Inborn_genetic_diseases|Hyperphosphatasemia_with_bone_disease|not_provided": 2,
    "Inborn_genetic_diseases|Hyperphosphatasemia_with_bone_disease": 1,
    "Hyperphosphatasemia_with_bone_disease|not_specified|not_provided": 1,
    "TNFRSF11B-related_disorder|not_provided|Hyperphosphatasemia_with_bone_disease": 1,
    "Inborn_genetic_diseases|not_provided|Hyperphosphatasemia_with_bone_disease": 1,
    "not_provided|TNFRSF11B-related_disorder": 1,
    "Hyperphosphatasemia_with_bone_disease|Inborn_genetic_diseases|not_provided": 1,
    "TNFRSF11B-related_disorder|not_provided": 1,
    "not_specified|Hyperphosphatasemia_with_bone_disease|not_provided": 1,
    "COLEC10-related_disorder|See_cases|3MC_syndrome_3": 1,
    "3MC_syndrome_3": 5,
    "COLEC10-related_disorder": 1,
    "COLEC10-related_disorder|not_provided": 1,
    "Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome|not_provided": 12,
    "TAF2-related_disorder|not_provided": 4,
    "not_specified|Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome|not_provided": 1,
    "Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome": 9,
    "Microcephaly|Inborn_genetic_diseases|TAF2-related_disorder": 1,
    "TAF2-related_disorder": 2,
    "Inborn_genetic_diseases|Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome|not_provided": 1,
    "TAF2-related_disorder|Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome|not_provided": 1,
    "not_provided|TAF2-related_disorder": 3,
    "Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome|not_specified|not_provided": 2,
    "TAF2-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome": 1,
    "not_provided|Microcephaly-thin_corpus_callosum-intellectual_disability_syndrome|not_specified": 1,
    "TBC1D31-related_disorder": 11,
    "OMIM:_606604": 1,
    "TMEM65-related_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_24": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_24|not_specified|not_provided": 1,
    "not_provided|NDUFB9-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_24": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_24|not_provided": 2,
    "Spastic_paraplegia|not_provided|not_specified": 6,
    "WASHC5-related_disorder": 7,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 136,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 119,
    "not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 10,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_provided": 1,
    "not_provided|WASHC5-related_disorder|Ritscher-Schinzel_syndrome_1": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_specified|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 3,
    "not_provided|Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome|WASHC5-related_disorder|not_specified|Ritscher-Schinzel_syndrome_1": 1,
    "Ritscher-Schinzel_syndrome_1": 10,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_specified": 2,
    "not_specified|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 3,
    "not_provided|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 3,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia": 1,
    "WASHC5-related_disorder|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 2,
    "WASHC5-related_disorder|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|WASHC5-related_disorder": 2,
    "Ritscher-Schinzel_syndrome_1|Hereditary_spastic_paraplegia_8": 2,
    "Ritscher-Schinzel_syndrome_1|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "not_specified|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_provided": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_provided": 16,
    "not_provided|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia": 2,
    "WASHC5-related_disorder|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_provided": 2,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_specified": 4,
    "Ritscher-Schinzel_syndrome_1|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Inborn_genetic_diseases": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_provided": 5,
    "Ritscher-Schinzel_syndrome_1|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 2,
    "not_provided|Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome_1|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "not_provided|Hereditary_spastic_paraplegia_8": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome|not_provided": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_specified|WASHC5-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 1,
    "Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_provided|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome_1|Ritscher-Schinzel_syndrome": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome_1": 2,
    "not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_specified": 1,
    "Hereditary_spastic_paraplegia_8|not_provided": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|WASHC5-related_disorder": 1,
    "Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_specified|not_provided": 2,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Inborn_genetic_diseases|not_provided": 2,
    "Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome|WASHC5-related_disorder|not_specified|not_provided": 3,
    "WASHC5-related_disorder|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "Muscle_weakness|Spastic_paraplegia|Spastic_gait|Headache|Equinovarus_deformity|Stress_urinary_incontinence|Loss_of_ambulation|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "Lower_limb_spasticity": 1,
    "not_provided|Hereditary_spastic_paraplegia_8|Hereditary_spastic_paraplegia|Ritscher-Schinzel_syndrome|WASHC5-related_disorder|not_specified": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_8|Incidental_Discovery": 1,
    "not_provided|WASHC5-related_disorder|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|Inborn_genetic_diseases|not_specified": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_provided|not_specified": 2,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_specified|not_provided|Ritscher-Schinzel_syndrome_1": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Spasticity": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Ritscher-Schinzel_syndrome_1": 1,
    "not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome_1": 1,
    "Hereditary_spastic_paraplegia_8|not_provided|Ritscher-Schinzel_syndrome|not_specified": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|Inborn_genetic_diseases|Ritscher-Schinzel_syndrome_1": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|WASHC5-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_specified": 1,
    "not_provided|Ritscher-Schinzel_syndrome_1": 1,
    "WASHC5-related_disorder|not_specified|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 1,
    "Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome|not_provided|not_specified": 1,
    "Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8|not_specified|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 2,
    "Inborn_genetic_diseases|Ritscher-Schinzel_syndrome_1": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_8|Ritscher-Schinzel_syndrome": 1,
    "not_provided|not_specified|Ritscher-Schinzel_syndrome|Hereditary_spastic_paraplegia_8": 1,
    "Hereditary_spastic_paraplegia_8|not_specified|not_provided": 1,
    "Seckel_syndrome_10": 3,
    "not_provided|Seckel_syndrome_10": 2,
    "NSMCE2-related_disorder|not_provided": 4,
    "Microcephaly|Decreased_response_to_growth_hormone_stimulation_test|Dysmorphic_features|Global_developmental_delay|Short_stature": 1,
    "not_provided|NSMCE2-related_disorder": 1,
    "Seckel_syndrome_10|not_provided": 1,
    "Familial_prostate_cancer": 14,
    "not_provided|Classic_Hodgkin_lymphoma|MYC-related_disorder": 1,
    "Burkitt_lymphoma": 3,
    "Cholesteatoma_of_middle_ear|Burkitt_lymphoma": 1,
    "Cholesteatoma_of_middle_ear": 4,
    "MYC-related_disorder": 2,
    "Glioma_susceptibility_7": 1,
    "EFR3A-related_disorder": 22,
    "EFR3A-related_disorder|not_specified": 1,
    "Seizures|_benign_familial_neonatal|_2|Benign_Neonatal_Epilepsy|not_provided": 1,
    "Seizures|_benign_familial_neonatal|_2": 89,
    "Benign_Neonatal_Epilepsy|Benign_neonatal_seizures": 13,
    "Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures": 45,
    "Seizures|_benign_familial_neonatal|_2|Benign_Neonatal_Epilepsy": 30,
    "not_provided|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures": 24,
    "not_provided|Seizures|_benign_familial_neonatal|_2|Benign_Neonatal_Epilepsy": 21,
    "Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|not_provided": 9,
    "Benign_Neonatal_Epilepsy|Seizures|_benign_familial_neonatal|_2": 1,
    "not_provided|Seizures|_benign_familial_neonatal|_2": 4,
    "Benign_Neonatal_Epilepsy|not_provided|Seizures|_benign_familial_neonatal|_2": 4,
    "Benign_neonatal_seizures|Benign_Neonatal_Epilepsy": 10,
    "Benign_neonatal_seizures": 601,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided|Seizures|_benign_familial_neonatal|_2": 2,
    "Seizures|_benign_familial_neonatal|_2|not_specified|Benign_neonatal_seizures": 2,
    "Benign_neonatal_seizures|not_provided": 50,
    "Benign_neonatal_seizures|not_specified": 24,
    "Benign_neonatal_seizures|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Benign_neonatal_seizures": 23,
    "Inborn_genetic_diseases|not_specified|Benign_neonatal_seizures": 1,
    "not_specified|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures": 2,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided|not_specified": 1,
    "not_provided|Benign_neonatal_seizures": 31,
    "not_provided|Inborn_genetic_diseases|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|Benign_Neonatal_Epilepsy": 1,
    "Benign_neonatal_seizures|KCNQ3-related_disorder": 5,
    "Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|KCNQ3-related_disorder": 1,
    "not_provided|Benign_neonatal_seizures|not_specified": 3,
    "Benign_neonatal_seizures|Inborn_genetic_diseases": 14,
    "not_specified|Benign_neonatal_seizures|not_provided": 2,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_specified|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "not_provided|Inborn_genetic_diseases|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2": 1,
    "Seizures|_benign_familial_neonatal|_2|Inborn_genetic_diseases|Benign_Neonatal_Epilepsy|Benign_neonatal_seizures|not_specified|not_provided": 1,
    "Benign_neonatal_seizures|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|KCNQ3-related_disorder|Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|Benign_Neonatal_Epilepsy": 2,
    "Benign_neonatal_seizures|not_specified|not_provided": 4,
    "Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2": 17,
    "Seizures|_benign_familial_neonatal|_2|KCNQ3-related_disorder|Benign_neonatal_seizures|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Benign_neonatal_seizures|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2": 1,
    "Seizures|_benign_familial_neonatal|_2|KCNQ3-related_disorder|Benign_neonatal_seizures|not_specified": 1,
    "Benign_neonatal_seizures|not_provided|Inborn_genetic_diseases": 1,
    "Benign_Neonatal_Epilepsy|Benign_neonatal_seizures|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "Benign_neonatal_seizures|Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_neonatal|_2": 5,
    "Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|not_provided": 1,
    "KCNQ3-related_disorder": 6,
    "not_provided|Benign_neonatal_seizures|Inborn_genetic_diseases": 4,
    "not_specified|Benign_neonatal_seizures": 12,
    "KCNQ3-related_disorder|Benign_neonatal_seizures|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Benign_neonatal_seizures": 2,
    "Benign_Neonatal_Epilepsy|Benign_neonatal_seizures|Inborn_genetic_diseases|not_specified|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided": 4,
    "KCNQ3-related_disorder|Benign_neonatal_seizures|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Benign_neonatal_seizures|Inborn_genetic_diseases|not_specified|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "Seizures|_benign_familial_neonatal|_2|Benign_Neonatal_Epilepsy|Benign_neonatal_seizures": 1,
    "Benign_Neonatal_Epilepsy|KCNQ3-related_disorder|Inborn_genetic_diseases|Benign_neonatal_seizures|not_specified|not_provided|Seizures|_benign_familial_neonatal|_2|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|not_provided": 1,
    "not_provided|not_specified|Seizures|_benign_familial_neonatal|_2": 1,
    "not_provided|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Benign_neonatal_seizures": 1,
    "KCNQ3-related_disorder|Benign_neonatal_seizures|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2": 1,
    "Benign_neonatal_seizures|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2|not_provided|Intellectual_disability": 1,
    "Benign_Neonatal_Epilepsy|Inborn_genetic_diseases|Benign_neonatal_seizures": 1,
    "Intellectual_disability|Seizure|not_provided|Benign_neonatal_seizures": 1,
    "not_provided|Seizures|_benign_familial_neonatal|_2|not_specified": 1,
    "Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|not_specified|KCNQ3-related_disorder": 1,
    "Benign_neonatal_seizures|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2|not_provided": 1,
    "not_specified|not_provided|Benign_neonatal_seizures": 1,
    "Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|Inborn_genetic_diseases|not_provided": 1,
    "Benign_neonatal_seizures|not_provided|Intellectual_disability": 1,
    "Benign_neonatal_seizures|not_provided|Seizures|_benign_familial_neonatal|_2|Benign_Neonatal_Epilepsy|Inborn_genetic_diseases|not_specified": 1,
    "Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|not_specified": 1,
    "Benign_neonatal_seizures|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|KCNQ3-related_disorder": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Seizures|_benign_familial_neonatal|_2": 1,
    "not_provided|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2": 2,
    "Benign_neonatal_seizures|not_specified|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2|not_provided": 1,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided|Seizures|_benign_familial_neonatal|_2|not_specified": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|Benign_neonatal_seizures": 1,
    "KCNQ3-related_disorder|not_provided|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures": 1,
    "Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|not_provided": 2,
    "Seizure|Benign_neonatal_seizures|not_provided": 1,
    "not_provided|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|KCNQ3-related_disorder": 1,
    "Seizures|_benign_familial_neonatal|_2|not_specified|Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided": 1,
    "not_provided|not_specified|Benign_neonatal_seizures": 1,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_specified|KCNQ3-related_disorder|not_provided": 1,
    "not_specified|Benign_neonatal_seizures|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|not_specified": 1,
    "Inborn_genetic_diseases|See_cases|Benign_neonatal_seizures|not_provided|Seizure|Seizures|_benign_familial_neonatal|_2": 1,
    "KCNQ3-related_Autism_and_developmental_disability|Intellectual_disability|Benign_neonatal_seizures|Lennox-Gastaut_syndrome|KCNQ3-related_developmental_disability|Neurodevelopmental_disorder|Seizures|_benign_familial_infantile|_5|Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_neonatal|_2|Intellectual_disability|_severe|Severe_neurodevelopmental_delay": 1,
    "Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_2|Benign_neonatal_seizures|not_provided|not_specified": 1,
    "Benign_neonatal_seizures|Seizures|_benign_familial_neonatal|_2|Inborn_genetic_diseases": 1,
    "Benign_neonatal_seizures|Inborn_genetic_diseases|not_specified": 2,
    "KCNQ3-related_disorder|Inborn_genetic_diseases|Benign_neonatal_seizures|not_provided": 1,
    "KCNQ3-related_disorder|not_provided": 1,
    "KCNQ3-associated_disorder|not_provided": 1,
    "KCNQ3-related_disorder|Benign_neonatal_seizures": 1,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_specified|not_provided": 1,
    "See_cases|Inborn_genetic_diseases|Benign_neonatal_seizures": 1,
    "Inborn_genetic_diseases|Benign_neonatal_seizures|not_specified": 1,
    "not_provided|KCNQ3-related_disorder|Benign_neonatal_seizures": 1,
    "KCNQ3-related_disorder|not_specified": 1,
    "KCNQ3-related_disorder|not_provided|Seizures|_benign_familial_neonatal|_2": 1,
    "Benign_neonatal_seizures|not_provided|Benign_Neonatal_Epilepsy": 1,
    "Benign_Neonatal_Epilepsy|Benign_neonatal_seizures|not_provided": 2,
    "Benign_Neonatal_Epilepsy|not_provided|Benign_neonatal_seizures": 1,
    "Primary_ciliary_dyskinesia_19|not_provided": 4,
    "Primary_ciliary_dyskinesia_19": 151,
    "not_provided|Primary_ciliary_dyskinesia_19": 1,
    "Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia": 20,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_19": 3,
    "Primary_ciliary_dyskinesia|not_provided|not_specified|Primary_ciliary_dyskinesia_19|Multiple_sclerosis|_susceptibility_to": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_19": 18,
    "not_provided|Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia": 2,
    "not_specified|Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Primary_ciliary_dyskinesia_19": 1,
    "Primary_ciliary_dyskinesia|DNAAF11-related_disorder": 2,
    "Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia_19|not_specified": 1,
    "DNAAF11-related_disorder": 2,
    "Primary_ciliary_dyskinesia|Kartagener_syndrome|DNAAF11-related_disorder|Primary_ciliary_dyskinesia_19": 1,
    "DNAAF11-related_disorder|Primary_ciliary_dyskinesia_19|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_19|Heterotaxy": 1,
    "not_specified|Primary_ciliary_dyskinesia_19": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_19|DNAAF11-related_disorder": 2,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided|Primary_ciliary_dyskinesia_19": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_19": 1,
    "Primary_ciliary_dyskinesia_19|DNAAF11-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_19|DNAAF11-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_19|not_provided": 1,
    "Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia|DNAAF11-related_disorder": 1,
    "Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia|not_provided|DNAAF11-related_disorder": 1,
    "Primary_ciliary_dyskinesia_19|Infertility_disorder|not_provided": 1,
    "not_provided|DNAAF11-related_disorder|Primary_ciliary_dyskinesia_19|Primary_ciliary_dyskinesia": 1,
    "Autoimmune_thyroid_disease|_susceptibility_to|_3": 5,
    "Iodotyrosyl_coupling_defect": 84,
    "not_provided|Iodotyrosyl_coupling_defect": 50,
    "Iodotyrosyl_coupling_defect|not_provided": 66,
    "not_provided|Autoimmune_thyroid_disease|_susceptibility_to|_3|Iodotyrosyl_coupling_defect": 1,
    "TG-related_disorder|not_provided": 8,
    "Iodotyrosyl_coupling_defect|TG-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Iodotyrosyl_coupling_defect": 12,
    "TG-related_disorder": 15,
    "not_provided|Iodotyrosyl_coupling_defect|TG-related_disorder": 3,
    "Autoimmune_thyroid_disease|_susceptibility_to|_3|Iodotyrosyl_coupling_defect": 35,
    "TG-related_disorder|not_provided|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_specified": 1,
    "not_provided|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3": 7,
    "not_provided|not_specified|Iodotyrosyl_coupling_defect": 9,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_provided": 15,
    "Autoimmune_thyroid_disease|_susceptibility_to|_3|Iodotyrosyl_coupling_defect|not_provided": 1,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_specified|not_provided": 3,
    "Iodotyrosyl_coupling_defect|Congenital_hypothyroidism": 1,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3": 3,
    "TG-related_disorder|Autoimmune_thyroid_disease|_susceptibility_to|_3|Iodotyrosyl_coupling_defect|not_provided|Congenital_hypothyroidism": 1,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|TG-related_disorder": 2,
    "not_provided|TG-related_disorder": 17,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|Inborn_genetic_diseases": 1,
    "Iodotyrosyl_coupling_defect|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|Iodotyrosyl_coupling_defect|TG-related_disorder": 1,
    "not_provided|Iodotyrosyl_coupling_defect|not_specified": 6,
    "not_provided|not_specified|TG-related_disorder|Iodotyrosyl_coupling_defect": 1,
    "Iodotyrosyl_coupling_defect|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Iodotyrosyl_coupling_defect|TG-related_disorder": 1,
    "Iodotyrosyl_coupling_defect|not_specified": 2,
    "not_provided|Iodotyrosyl_coupling_defect|not_specified|Autoimmune_thyroid_disease|_susceptibility_to|_3": 1,
    "not_provided|TG-related_disorder|Iodotyrosyl_coupling_defect": 1,
    "Iodotyrosyl_coupling_defect|not_provided|Autoimmune_thyroid_disease|_susceptibility_to|_3|Inborn_genetic_diseases": 1,
    "Premature_ovarian_failure|not_provided|Iodotyrosyl_coupling_defect": 1,
    "Inborn_genetic_diseases|TG-related_disorder": 1,
    "Iodotyrosyl_coupling_defect|not_provided|Autoimmune_thyroid_disease|_susceptibility_to|_3": 1,
    "TG-related_disorder|not_provided|Iodotyrosyl_coupling_defect": 2,
    "not_provided|Inborn_genetic_diseases|Iodotyrosyl_coupling_defect": 3,
    "Iodotyrosyl_coupling_defect|TG-related_disorder": 1,
    "not_specified|not_provided|Iodotyrosyl_coupling_defect": 7,
    "not_specified|Iodotyrosyl_coupling_defect": 2,
    "not_specified|Iodotyrosyl_coupling_defect|not_provided|Autoimmune_thyroid_disease|_susceptibility_to|_3": 1,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Thyroid_dyshormonogenesis|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Iodotyrosyl_coupling_defect": 1,
    "not_specified|Iodotyrosyl_coupling_defect|not_provided": 3,
    "Inborn_genetic_diseases|Iodotyrosyl_coupling_defect|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Iodotyrosyl_coupling_defect": 1,
    "Iodotyrosyl_coupling_defect|not_provided|TG-related_disorder": 5,
    "Iodotyrosyl_coupling_defect|not_specified|not_provided": 3,
    "not_provided|TG-related_disorder|Inborn_genetic_diseases": 1,
    "TG-related_disorder|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_provided|Congenital_hypothyroidism": 1,
    "TG-related_disorder|Inborn_genetic_diseases|Iodotyrosyl_coupling_defect|not_provided": 1,
    "Congenital_hypothyroidism|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3": 1,
    "Iodotyrosyl_coupling_defect|not_provided|Congenital_hypothyroidism": 1,
    "TG-related_disorder|not_provided|Iodotyrosyl_coupling_defect|Congenital_hypothyroidism": 1,
    "Hypothyroidism": 1,
    "Iodotyrosyl_coupling_defect|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3": 1,
    "TG-related_disorder|Inborn_genetic_diseases": 1,
    "Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3|not_specified": 1,
    "TG-related_disorder|Iodotyrosyl_coupling_defect": 1,
    "TG-related_disorder|Iodotyrosyl_coupling_defect|Autoimmune_thyroid_disease|_susceptibility_to|_3": 1,
    "Iodotyrosyl_coupling_defect|not_provided|Inborn_genetic_diseases": 2,
    "Thyroid_dyshormonogenesis": 1,
    "not_specified|TG-related_disorder|not_provided|Iodotyrosyl_coupling_defect": 1,
    "Charcot-Marie-Tooth_disease_type_4D": 79,
    "not_provided|Charcot-Marie-Tooth_disease_type_4D": 12,
    "Charcot-Marie-Tooth_disease_type_4D|not_specified": 2,
    "Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4": 17,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4": 2,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D": 3,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4": 8,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|NDRG1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D": 32,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D": 3,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 4,
    "Charcot-Marie-Tooth_disease_type_4D|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D": 5,
    "Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease": 5,
    "not_specified|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|Inborn_genetic_diseases": 4,
    "Charcot-Marie-Tooth_disease_type_4D|not_provided": 6,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|not_specified": 1,
    "NDRG1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|NDRG1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4D|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4D": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4D|NDRG1-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|NDRG1-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|NDRG1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D": 3,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4D|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|NDRG1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "NDRG1-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4D|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|NDRG1-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|NDRG1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4D|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NDRG1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4D": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4D": 1,
    "NDRG1-related_disorder|Charcot-Marie-Tooth_disease_type_4D|not_specified": 1,
    "Birk-Barel_Intellectual_Disability_Dysmorphism_Syndrome": 1,
    "Birk-Barel_syndrome": 10,
    "not_provided|Birk-Barel_syndrome": 3,
    "KCNK9-related_disorder": 4,
    "not_provided|KCNK9-related_disorder": 2,
    "Birk-Barel_syndrome|not_provided": 2,
    "Birk-Barel_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "KCNK9-related_disorder|not_provided": 1,
    "TRAPPC9-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_provided|not_specified|Intellectual_disability": 1,
    "not_specified|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_provided|TRAPPC9-related_disorder": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_provided|TRAPPC9-related_disorder|not_specified|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_provided|Intellectual_Disability|_Recessive|TRAPPC9-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_Disability|_Recessive|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_13|not_provided": 8,
    "not_specified|Intellectual_disability|_autosomal_recessive_13|Inborn_genetic_diseases|not_provided": 3,
    "Intellectual_disability|_autosomal_recessive_13": 48,
    "TRAPPC9-related_disorder|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|TRAPPC9-related_disorder": 1,
    "not_specified|Intellectual_Disability|_Recessive|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_13|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_recessive_13": 1,
    "Intellectual_disability|_autosomal_recessive_13|not_specified|not_provided|Inborn_genetic_diseases|TRAPPC9-related_disorder|Intellectual_Disability|_Recessive": 1,
    "not_specified|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|Intellectual_disability-obesity-brain_malformations-facial_dysmorphism_syndrome|not_provided": 1,
    "TRAPPC9-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_13": 1,
    "Intellectual_Disability|_Recessive|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_13|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_13|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_specified": 2,
    "TRAPPC9-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TRAPPC9-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_recessive_13|not_provided": 1,
    "TRAPPC9-related_disorder|not_provided": 7,
    "not_provided|Intellectual_disability|_autosomal_recessive_13": 9,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_13": 3,
    "TRAPPC9-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_provided": 2,
    "Autism_spectrum_disorder|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_provided|TRAPPC9-related_disorder": 4,
    "Intellectual_disability|_autosomal_recessive_13|not_specified|not_provided|Inborn_genetic_diseases|TRAPPC9-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_Disability|_Recessive": 1,
    "TRAPPC9-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_13|not_provided": 1,
    "not_provided|Intellectual_disability-obesity-brain_malformations-facial_dysmorphism_syndrome": 1,
    "not_provided|not_specified|Intellectual_Disability|_Recessive|Inborn_genetic_diseases": 3,
    "not_provided|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_specified": 1,
    "TRAPPC9-related_disorder|Intellectual_Disability|_Recessive|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_Disability|_Recessive": 3,
    "TRAPPC9-related_disorder|Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_provided": 1,
    "TRAPPC9-related_disorder": 7,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_13|TRAPPC9-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_13|Intellectual_Disability|_Recessive": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_13|not_specified": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_13|Inborn_genetic_diseases": 1,
    "not_provided|Abnormality_of_the_nervous_system|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_13|not_provided": 2,
    "not_specified|not_provided|Intellectual_Disability|_Recessive|Inborn_genetic_diseases": 3,
    "TRAPPC9-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_Disability|_Recessive|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_recessive_13|not_specified|not_provided": 1,
    "not_specified|not_provided|Intellectual_Disability|_Recessive|TRAPPC9-related_disorder|Inborn_genetic_diseases": 1,
    "TRAPPC9-related_disorder|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_provided": 1,
    "TRAPPC9-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_13|Intellectual_Disability|_Recessive|not_provided": 2,
    "TRAPPC9-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_13|not_specified|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_13|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_13|Abnormality_of_the_nervous_system": 1,
    "Intellectual_disability|_autosomal_recessive_13|not_specified|Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_provided|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|Intellectual_disability|_autosomal_recessive_13|Intellectual_Disability|_Recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_13|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_13": 1,
    "Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_specified|not_provided|TRAPPC9-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Intellectual_Disability|_Recessive": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_Disability|_Recessive|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_13": 2,
    "not_specified|Intellectual_disability|_autosomal_recessive_13|Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_recessive_13": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Intellectual_disability|Intellectual_Disability|_Recessive|TRAPPC9-related_disorder|Intellectual_disability|_autosomal_recessive_13": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_13|Intellectual_Disability|_Recessive|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_13|Intellectual_disability": 1,
    "Intellectual_Disability|_Recessive|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_Disability|_Recessive|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_13": 1,
    "Intellectual_disability|_autosomal_recessive_13|Inborn_genetic_diseases|not_provided": 1,
    "History_of_neurodevelopmental_disorder|Intellectual_disability|_autosomal_recessive_13|TRAPPC9-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_Disability|_Recessive|not_specified|not_provided": 1,
    "not_provided|not_specified|TRAPPC9-related_disorder": 1,
    "Lessel-Kreienkamp_syndrome": 20,
    "AGO2-related_disorder": 5,
    "Lessel-Kreienkamp_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "AGO2-related_disorder|not_specified": 1,
    "Lessel-Kreienkamp_syndrome|not_provided": 2,
    "not_provided|Lessel-Kreienkamp_syndrome": 2,
    "Inborn_genetic_diseases|Lessel-Kreienkamp_syndrome|not_provided": 1,
    "not_provided|AGO2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Lessel-Kreienkamp_syndrome": 1,
    "Inborn_genetic_diseases|Lessel-Kreienkamp_syndrome": 1,
    "Epicanthus|Autism|Hypotonia|Shallow_orbits|Mandibular_prognathia|Bulbous_nose|Deeply_set_eye|Dental_crowding|High_palate|Hypertonia|Failure_to_thrive": 1,
    "Acroerythrokeratoderma": 19,
    "not_provided|Acroerythrokeratoderma": 5,
    "SLURP1-related_disorder": 1,
    "not_specified|Acroerythrokeratoderma": 2,
    "not_specified|not_provided|Acroerythrokeratoderma": 1,
    "not_provided|Acroerythrokeratoderma|SLURP1-related_disorder": 1,
    "not_provided|Autism|not_specified": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism": 99,
    "not_provided|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism": 24,
    "Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 26,
    "Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Glucocorticoid-remediable_aldosteronism": 9,
    "Glucocorticoid-remediable_aldosteronism|Congenital_adrenal_hyperplasia": 3,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 18,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_specified": 6,
    "Deficiency_of_steroid_11-beta-monooxygenase|CYP11B1-related_disorder": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|not_provided": 19,
    "Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_specified|not_provided": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided": 27,
    "Deficiency_of_steroid_11-beta-monooxygenase": 74,
    "Glucocorticoid-remediable_aldosteronism": 1,
    "not_specified|not_provided|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism": 2,
    "Congenital_adrenal_hyperplasia|not_provided|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Congenital_adrenal_hyperplasia|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "not_provided|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|Congenital_adrenal_hyperplasia": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|Congenital_adrenal_hyperplasia": 1,
    "Congenital_adrenal_hyperplasia|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided": 2,
    "CYP11B1-related_disorder|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_provided": 2,
    "not_provided|Deficiency_of_steroid_11-beta-monooxygenase": 8,
    "Inborn_genetic_diseases|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 3,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism": 5,
    "Deficiency_of_steroid_11-beta-monooxygenase|Inborn_genetic_diseases": 1,
    "Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_provided": 7,
    "not_provided|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|CYP11B1-related_disorder": 2,
    "not_provided|Glucocorticoid-remediable_aldosteronism": 2,
    "Deficiency_of_steroid_11-beta-monooxygenase|Congenital_adrenal_hyperplasia|Glucocorticoid-remediable_aldosteronism": 1,
    "Congenital_adrenal_hyperplasia|not_provided|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "CYP11B1-related_disorder|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided": 1,
    "not_provided|not_specified|Congenital_adrenal_hyperplasia|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided|Congenital_adrenal_hyperplasia": 3,
    "Deficiency_of_steroid_11-beta-monooxygenase|CYP11B1-related_disorder|not_provided": 1,
    "Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|Congenital_adrenal_hyperplasia": 2,
    "Deficiency_of_steroid_11-beta-monooxygenase|Inborn_genetic_diseases|Glucocorticoid-remediable_aldosteronism": 1,
    "Congenital_adrenal_hyperplasia|Inborn_genetic_diseases": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|Inborn_genetic_diseases|Congenital_adrenal_hyperplasia|not_specified": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Glucocorticoid-remediable_aldosteronism|not_specified": 3,
    "not_specified|not_provided|Congenital_adrenal_hyperplasia|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Glucocorticoid-remediable_aldosteronism|not_provided|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Congenital_adrenal_hyperplasia|Deficiency_of_steroid_11-beta-monooxygenase|not_provided|CYP11B1-related_disorder": 1,
    "Congenital_adrenal_hyperplasia|Deficiency_of_steroid_11-beta-monooxygenase|not_provided": 1,
    "CYP11B1-related_disorder|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Congenital_adrenal_hyperplasia": 1,
    "CYP11B1-related_disorder|Inborn_genetic_diseases": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|Congenital_adrenal_hyperplasia|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Inborn_genetic_diseases|not_provided|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|Inborn_genetic_diseases": 1,
    "Glucocorticoid-remediable_aldosteronism|not_specified": 1,
    "not_specified|Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Glucocorticoid-remediable_aldosteronism": 5,
    "not_provided|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_specified": 2,
    "Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "CYP11B1-related_disorder|not_provided|Congenital_adrenal_hyperplasia|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "not_provided|Congenital_adrenal_hyperplasia|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided|not_specified": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Congenital_adrenal_hyperplasia": 2,
    "not_provided|not_specified|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism": 1,
    "not_provided|not_specified|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase": 1,
    "Inborn_genetic_diseases|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided": 2,
    "Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Glucocorticoid-remediable_aldosteronism|Inborn_genetic_diseases": 1,
    "CYP11B1-related_disorder|not_provided": 1,
    "not_provided|Deficiency_of_steroid_11-beta-monooxygenase|Congenital_adrenal_hyperplasia|Glucocorticoid-remediable_aldosteronism": 1,
    "not_specified|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_provided": 1,
    "Inborn_genetic_diseases|CYP11B1-related_disorder": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|not_provided|Congenital_adrenal_hyperplasia": 1,
    "Inborn_genetic_diseases|Glucocorticoid-remediable_aldosteronism|Deficiency_of_steroid_11-beta-monooxygenase|not_specified": 1,
    "Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism|not_specified": 1,
    "CYP11B1-related_disorder|Deficiency_of_steroid_11-beta-monooxygenase|Glucocorticoid-remediable_aldosteronism": 1,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency": 4,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Glucocorticoid-remediable_aldosteronism": 14,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency": 8,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 11,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 2,
    "Corticosterone_methyloxidase_type_2_deficiency|Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency": 4,
    "Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency": 2,
    "not_provided|Corticosterone_methyloxidase_type_2_deficiency|Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency": 1,
    "Corticosterone_methyl_oxidase_type_II_deficiency": 41,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 59,
    "CYP11B2-related_disorder|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "CYP11B2-related_disorder": 12,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Inborn_genetic_diseases": 2,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Inborn_genetic_diseases|Glucocorticoid-remediable_aldosteronism": 1,
    "Corticosterone_methyl_oxidase_type_II_deficiency|not_provided": 21,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Inborn_genetic_diseases": 8,
    "not_provided|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism": 1,
    "Corticosterone_18-monooxygenase_deficiency": 5,
    "not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency": 6,
    "not_specified|not_provided|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism": 1,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|CYP11B2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency": 6,
    "not_specified|not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|not_provided": 17,
    "CYP11B2-related_disorder|not_provided": 1,
    "not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 15,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyl_oxidase_type_II_deficiency": 1,
    "Aldosterone_Synthase_Deficiency": 1,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 2,
    "not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Glucocorticoid-remediable_aldosteronism": 2,
    "not_provided|Corticosterone_methyl_oxidase_type_II_deficiency": 11,
    "Corticosterone_18-monooxygenase_deficiency|not_provided|Corticosterone_methyloxidase_type_2_deficiency": 5,
    "not_specified|not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency": 3,
    "not_specified|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 2,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|not_provided": 1,
    "Corticosterone_methyl_oxidase_type_II_deficiency|not_specified|not_provided": 1,
    "Glucocorticoid-remediable_aldosteronism|Inborn_genetic_diseases|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency": 1,
    "not_provided|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Inborn_genetic_diseases|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 2,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|not_provided|Glucocorticoid-remediable_aldosteronism": 1,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Glucocorticoid-remediable_aldosteronism|not_provided": 1,
    "Corticosterone_methyloxidase_type_2_deficiency": 2,
    "not_provided|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Glucocorticoid-remediable_aldosteronism|not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency": 5,
    "Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|not_provided": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|not_provided": 3,
    "CYP11B2-related_disorder|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|not_provided": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|not_provided|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism": 4,
    "Familial_hypoaldosteronism": 1,
    "CYP11B2-related_disorder|Corticosterone_18-monooxygenase_deficiency|not_provided": 1,
    "not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency": 2,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism|Inborn_genetic_diseases": 1,
    "not_provided|Corticosterone_18-monooxygenase_deficiency": 2,
    "not_specified|not_provided|Corticosterone_methyl_oxidase_type_II_deficiency": 1,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Inborn_genetic_diseases": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|not_provided|CYP11B2-related_disorder": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|not_provided|CYP11B2-related_disorder": 1,
    "Corticosterone_methyl_oxidase_type_II_deficiency|not_provided|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency": 2,
    "not_provided|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyl_oxidase_type_II_deficiency": 1,
    "not_provided|Hypoaldosteronism|_congenital|Corticosterone_methyl_oxidase_type_II_deficiency": 1,
    "not_specified|not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency": 2,
    "Inborn_genetic_diseases|Corticosterone_methyl_oxidase_type_II_deficiency": 1,
    "not_provided|CYP11B2-related_disorder|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "not_provided|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|CYP11B2-related_disorder": 1,
    "Early-onset_familial_hypoaldosteronism|Corticosterone_methyl_oxidase_type_II_deficiency|not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|not_provided|Corticosterone_18-monooxygenase_deficiency": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency": 3,
    "Corticosterone_18-monooxygenase_deficiency|not_specified": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|not_provided|Glucocorticoid-remediable_aldosteronism": 1,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|not_provided|Corticosterone_18-monooxygenase_deficiency": 4,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|not_provided": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency": 1,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|not_provided|Hypoaldosteronism|_congenital|Corticosterone_18-monooxygenase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|CYP11B2-related_disorder": 1,
    "Corticosterone_18-monooxygenase_deficiency|not_provided": 3,
    "not_specified|Corticosterone_methyl_oxidase_type_II_deficiency|not_provided": 1,
    "Corticosterone_18-monooxygenase_deficiency|not_provided|Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Glucocorticoid-remediable_aldosteronism|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|not_provided": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|not_specified|not_provided": 1,
    "not_specified|not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency": 1,
    "Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_methyl_oxidase_type_II_deficiency|not_specified": 1,
    "Corticosterone_methyl_oxidase_type_II_deficiency|Corticosterone_18-monooxygenase_deficiency|Corticosterone_methyloxidase_type_2_deficiency|not_provided|not_specified|Glucocorticoid-remediable_aldosteronism": 1,
    "Corticosterone_methyloxidase_type_2_deficiency|Corticosterone_18-monooxygenase_deficiency|Glucocorticoid-remediable_aldosteronism": 1,
    "Aldosterone_to_renin_ratio|_increased": 1,
    "GPIHBP1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Hyperlipoproteinemia|_type_1D": 16,
    "Hyperlipoproteinemia|_type_1D|Cardiovascular_phenotype": 1,
    "Hyperlipoproteinemia|_type_1D|not_provided": 2,
    "Hyperlipoproteinemia|_type_1D|Hyperlipoproteinemia|_type_I": 1,
    "GPIHBP1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|not_provided|GPIHBP1-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|GPIHBP1-related_disorder": 1,
    "not_provided|Hyperlipoproteinemia|_type_1D": 1,
    "Hyperlipoproteinemia|_type_1D|Cardiovascular_phenotype|GPIHBP1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|GPIHBP1-related_disorder|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|GPIHBP1-related_disorder": 1,
    "Cardiovascular_phenotype|GPIHBP1-related_disorder|Hyperlipoproteinemia|_type_1D|not_provided": 1,
    "Sensorineural_hearing_loss_disorder|Premature_ovarian_insufficiency": 2,
    "MAFA-related_disorder": 8,
    "Osteopetrosis|_autosomal_dominant_3|not_specified": 1,
    "Islet_cell_adenomatosis": 6,
    "Juvenile-onset_diabetes_mellitus-central_and_peripheral_neurodegeneration_syndrome": 8,
    "Islet_cell_adenomatosis|MAFA-related_disorder|not_specified": 1,
    "Decreased_total_neutrophil_count|Decreased_total_lymphocyte_count|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_thin_corpus_callosum|_hypotonia|_and_absent_language": 2,
    "EEF1D-related_disorder": 11,
    "EEF1D-related_intellectual_disabilities": 2,
    "Neurodevelopmental_disorder_with_thin_corpus_callosum|_hypotonia|_and_absent_language": 2,
    "not_provided|Neurodevelopmental_disorder|not_specified": 1,
    "Myelodysplastic_syndrome_associated_with_isolated_del(5q)": 1,
    "EEF1D-related_disorder|not_provided": 6,
    "EEF1D-associated_Neurodevelopmental_Syndrome|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_thin_corpus_callosum|_hypotonia|_and_absent_language|Autosomal_recessive_non-syndromic_intellectual_disability": 1,
    "FAM83H-related_disorder": 17,
    "not_specified|not_provided|Amelogenesis_imperfecta|_hypocalcification_type": 1,
    "X-linked_amelogenesis_imperfecta_hypoplastic/hypomaturation_2": 6,
    "FAM83H-related_disorder|not_provided": 1,
    "not_provided|FAM83H-related_disorder": 1,
    "not_provided|Amelogenesis_imperfecta|_type_3A|Amelogenesis_imperfecta|_hypocalcification_type": 1,
    "Amelogenesis_imperfecta|_hypocalcification_type": 11,
    "not_provided|not_specified|Amelogenesis_imperfecta|_hypocalcification_type": 2,
    "Amelogenesis_imperfecta|_hypocalcification_type|FAM83H-related_disorder|not_provided": 1,
    "Amelogenesis_imperfecta|_hypocalcification_type|Amelogenesis_imperfecta|_type_3A": 2,
    "Amelogenesis_imperfecta|_type_3A|Amelogenesis_imperfecta|_hypocalcification_type": 1,
    "FAM83H-related_disorder|Amelogenesis_imperfecta|_type_3A": 1,
    "Amelogenesis_imperfecta|_type_3A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|FAM83H-related_disorder": 2,
    "Amelogenesis_imperfecta|_type_3A|Marfanoid_habitus_and_intellectual_disability|Inborn_genetic_diseases": 1,
    "FAM83H-related_disorder|not_specified|not_provided|Amelogenesis_imperfecta|_type_3A": 1,
    "SCRIB-related_disorder": 45,
    "not_provided|SCRIB-related_disorder": 4,
    "SCRIB-related_disorder|not_specified": 2,
    "SCRIB-related_disorder|not_provided": 1,
    "SCRIB-related_disorder|EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_provided": 1,
    "PUF60-related_disorder|Neurodevelopmental_abnormality|not_provided": 1,
    "Intellectual_disability-cardiac_anomalies-short_stature-joint_laxity_syndrome": 2,
    "8q24.3_microdeletion_syndrome": 59,
    "PUF60-related_disorder": 9,
    "Inborn_genetic_diseases|PUF60-related_disorder": 2,
    "8q24.3_microdeletion_syndrome|Inborn_genetic_diseases": 1,
    "8q24.3_microdeletion_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|8q24.3_microdeletion_syndrome": 2,
    "not_provided|8q24.3_microdeletion_syndrome": 7,
    "Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities": 74,
    "8q24.3_microdeletion_syndrome|not_provided": 9,
    "8q24.3_microdeletion_syndrome|not_provided|See_cases": 1,
    "not_provided|PUF60-related_disorder|Syndromic_intellectual_disability": 1,
    "Intellectual_disability-cardiac_anomalies-short_stature-joint_laxity_syndrome|not_provided": 1,
    "not_provided|PUF60-related_disorder": 1,
    "8q24.3_microdeletion_syndrome|Intellectual_disability-cardiac_anomalies-short_stature-joint_laxity_syndrome": 1,
    "Intellectual_disability|8q24.3_microdeletion_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|8q24.3_microdeletion_syndrome": 2,
    "Intellectual_disability-cardiac_anomalies-short_stature-joint_laxity_syndrome|Inborn_genetic_diseases": 1,
    "8q24.3_microdeletion_syndrome|not_provided|CHARGE_syndrome": 1,
    "PUF60-related_disorder|8q24.3_microdeletion_syndrome": 1,
    "not_specified|not_provided|8q24.3_microdeletion_syndrome": 1,
    "PUF60-related_disorder|8q24.3_microdeletion_syndrome|Inborn_genetic_diseases": 1,
    "EPPK1-related_disorder": 173,
    "EPPK1-related_disorder|not_specified": 11,
    "not_provided|EPPK1-related_disorder": 7,
    "EPPK1-related_disorder|not_provided": 6,
    "Myoepithelial_tumor|not_specified": 4,
    "not_specified|EPPK1-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 106,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 24,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 27,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 76,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 100,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 48,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 13,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 43,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 74,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 25,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 85,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 66,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 5,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 49,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 204,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 16,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 12,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 47,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 6,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 5,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 3,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 9,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 96,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 33,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 164,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 6,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 24,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 66,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 11,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 36,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 16,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 5,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 74,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 26,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 89,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 18,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 55,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 5,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 31,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 313,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 29,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 7,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 4,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 6,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 9,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 20,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 4,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 9,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 10,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 17,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 17,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 7,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 34,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 35,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 26,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 14,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 37,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 20,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 9,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 5,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 82,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 8,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 34,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 14,
    "not_provided|not_specified|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 47,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 22,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 4,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 11,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 21,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 26,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 38,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 21,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 4,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 15,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 15,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 3,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 8,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 4,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 31,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 6,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 13,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_specified|not_provided|Multiple_sclerosis": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 31,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 7,
    "PLEC-related_disorder|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 49,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 12,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 4,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 79,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 11,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 6,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 47,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 17,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Multiple_sclerosis|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 6,
    "not_provided|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 11,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 22,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 3,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 16,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 15,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 8,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 2,
    "not_specified|PLEC-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 15,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 12,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 27,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|PLEC-related_disorder": 5,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|PLEC-related_disorder": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 23,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 11,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 15,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 18,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|PLEC-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Multiple_sclerosis": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 8,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 11,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 5,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 12,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 12,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 17,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 7,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|PLEC-related_disorder": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 7,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 11,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder|not_specified|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 13,
    "PLEC-related_disorder": 34,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 3,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 23,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 6,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 7,
    "PLEC-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 11,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 13,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 4,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 6,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 11,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 9,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 8,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 6,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 8,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 5,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided|PLEC-related_disorder": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 3,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 3,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 5,
    "not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 2,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 9,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 11,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 16,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 8,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 5,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 34,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 5,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 55,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 15,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 4,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided": 7,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 10,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 8,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 3,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 16,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 3,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 7,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 5,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 8,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 13,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|PLEC-related_disorder": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 4,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "PLEC-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 16,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|PLEC-related_disorder|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 4,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|PLEC-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 10,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 3,
    "not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 13,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided": 24,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 15,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 5,
    "not_specified|not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_specified|PLEC-related_epidermolysis_bullosa|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 21,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 20,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 4,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 21,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 8,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 5,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 27,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 6,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 4,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 5,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 10,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "PLEC-related_disorder|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 3,
    "not_specified|not_provided|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|See_cases": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 5,
    "PLEC-related_disorder|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|PLEC-related_disorder": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|not_specified": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|not_specified": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 7,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 4,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 11,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 9,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided|See_cases": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 10,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 6,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 2,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 3,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 5,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_specified": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided|PLEC-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided|PLEC-related_disorder": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 3,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|PLEC-related_disorder": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 4,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|PLEC-related_disorder|not_provided": 2,
    "not_provided|Primary_dilated_cardiomyopathy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 9,
    "Epidermolysis_bullosa_simplex": 43,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 4,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 4,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 4,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|PLEC-related_disorder": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|not_specified": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "PLEC-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|not_provided": 3,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|PLEC-related_disorder": 2,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 3,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases|PLEC-related_disorder": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|not_specified": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "PLEC-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|not_specified": 2,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|See_cases|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Inborn_genetic_diseases|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 4,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 7,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 3,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided|PLEC-related_disorder": 1,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Multiple_sclerosis": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 10,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 2,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 7,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 8,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|PLEC-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 3,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 4,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 3,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 2,
    "not_provided|Cholestasis": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder|not_specified|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 2,
    "not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_provided|PLEC-related_disorder|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 3,
    "Myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|PLEC-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 5,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|PLEC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_specified|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "PLEC-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 3,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 4,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|PLEC-related_disorder|not_provided": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|PLEC-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided|PLEC-related_disorder": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 4,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "not_provided|PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|PLEC-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 3,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "See_cases|not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|PLEC-related_disorder": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided|PLEC-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 1,
    "Simplex_epidermolysis_bullosa_Ogna_type|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 6,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified": 4,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided": 2,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|PLEC-related_disorder|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_specified": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder": 2,
    "not_specified|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "Multiple_sclerosis|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 3,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases": 2,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_specified": 2,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|not_specified|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 2,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 1,
    "PLEC-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|PLEC-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 2,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 3,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 3,
    "Multiple_sclerosis|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "not_provided|PLEC-related_disorder|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_specified|not_provided": 2,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|PLEC-related_disorder": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|PLEC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|PLEC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 3,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 2,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|not_provided": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_disorder|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified": 1,
    "PLEC-related_disorder|not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|not_specified": 1,
    "not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 1,
    "not_specified|PLEC-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_specified|not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|PLEC-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PLEC-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided": 2,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Limb-girdle_muscular_dystrophy": 2,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|not_specified|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_plectin": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|PLEC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_provided": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_provided|PLEC-related_disorder|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "not_provided|PLEC-related_disorder|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_specified|PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases|PLEC-related_disorder|not_provided": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|PLEC-related_disorder": 2,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|PLEC-related_disorder": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_specified|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_with_nail_dystrophy|PLEC-related_epidermolysis_bullosa|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|not_specified": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_specified|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|not_specified": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "PLEC-related_disorder|not_specified": 1,
    "not_provided|PLEC-related_disorder|not_specified": 4,
    "not_specified|PLEC-related_disorder": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "not_specified|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy": 1,
    "PLEC-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q": 1,
    "Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Abnormality_of_the_musculature": 1,
    "Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "not_specified|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia": 1,
    "PLEC-related_disorder|not_provided|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex|_Ogna_type|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy": 1,
    "not_provided|Epidermolysis_bullosa_simplex_5C|_with_pyloric_atresia|Epidermolysis_bullosa_simplex|_Ogna_type|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2Q|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Epidermolysis_bullosa_simplex_5B|_with_muscular_dystrophy|not_specified": 1,
    "5-Oxoprolinase_deficiency": 296,
    "OPLAH-related_disorder": 6,
    "not_provided|5-Oxoprolinase_deficiency": 9,
    "5-Oxoprolinase_deficiency|not_provided": 14,
    "not_specified|5-Oxoprolinase_deficiency": 22,
    "OPLAH-related_disorder|5-Oxoprolinase_deficiency": 9,
    "not_provided|5-Oxoprolinase_deficiency|OPLAH-related_disorder": 4,
    "5-Oxoprolinase_deficiency|not_specified": 18,
    "5-Oxoprolinase_deficiency|OPLAH-related_disorder": 4,
    "OPLAH-related_disorder|not_specified": 1,
    "not_provided|not_specified|5-Oxoprolinase_deficiency": 1,
    "5-Oxoprolinase_deficiency|not_provided|OPLAH-related_disorder": 4,
    "not_specified|5-Oxoprolinase_deficiency|not_provided": 1,
    "not_specified|See_cases|5-Oxoprolinase_deficiency": 1,
    "not_provided|5-Oxoprolinase_deficiency|not_specified": 1,
    "5-Oxoprolinase_deficiency|OPLAH-related_disorder|not_provided": 4,
    "5-Oxoprolinase_deficiency|not_specified|not_provided": 1,
    "not_specified|not_provided|5-Oxoprolinase_deficiency": 1,
    "not_specified|OPLAH-related_disorder": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15": 13,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15|Inborn_genetic_diseases": 1,
    "not_provided|Glycosylphosphatidylinositol_biosynthesis_defect_15": 9,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|GPAA1-related_disorder": 1,
    "GPAA1-related_disorder": 4,
    "GPAA1-related_disorder|not_provided": 9,
    "not_provided|Glycosylphosphatidylinositol_biosynthesis_defect_15|GPAA1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Glycosylphosphatidylinositol_biosynthesis_defect_15": 2,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15|not_provided": 4,
    "Inborn_genetic_diseases|GPAA1-related_disorder|not_provided": 1,
    "not_provided|GPAA1-related_disorder": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15|Inborn_genetic_diseases|not_specified|not_provided|See_cases": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Glycosylphosphatidylinositol_biosynthesis_defect_15|not_provided": 1,
    "Inborn_genetic_diseases|Glycosylphosphatidylinositol_biosynthesis_defect_15": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_15|not_provided|GPAA1-related_disorder": 1,
    "not_specified|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_6": 1,
    "CYC1-related_disorder|not_provided": 6,
    "Mitochondrial_complex_III_deficiency_nuclear_type_6|not_provided|not_specified": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_6|not_provided": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_6": 2,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_6": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_6|not_provided|CYC1-related_disorder|not_specified": 1,
    "not_specified|CYC1-related_disorder|not_provided": 1,
    "Autoinflammation_with_episodic_fever_and_immune_dysregulation": 2,
    "Congenital_diarrhea_7_with_exudative_enteropathy": 20,
    "not_provided|Congenital_diarrhea_7_with_exudative_enteropathy": 5,
    "not_provided|DGAT1-related_disorder": 8,
    "not_provided|Diarrhea|Congenital_diarrhea_7_with_exudative_enteropathy": 1,
    "Congenital_diarrhea_7_with_exudative_enteropathy|not_provided": 7,
    "DGAT1-related_disorder|not_provided": 4,
    "Congenital_diarrhea_7_with_exudative_enteropathy|DGAT1-related_disorder": 2,
    "DGAT1-related_disorder|Congenital_diarrhea_7_with_exudative_enteropathy|not_provided": 1,
    "DGAT1-related_disorder|Inborn_genetic_diseases|Congenital_diarrhea_7_with_exudative_enteropathy|not_provided": 1,
    "Congenital_diarrhea_7_with_exudative_enteropathy|See_cases|not_provided": 1,
    "DGAT1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_diarrhea_7_with_exudative_enteropathy": 1,
    "not_specified|Congenital_diarrhea_7_with_exudative_enteropathy": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|not_provided|not_specified": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_2": 19,
    "Brown-Vialetto-van_Laere_syndrome_2": 305,
    "Brown-Vialetto-van_Laere_syndrome_2|not_provided|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Brown-Vialetto-van_Laere_syndrome_2": 4,
    "Brown-Vialetto-van_Laere_syndrome_2|not_specified|Inborn_genetic_diseases": 3,
    "Brown-Vialetto-van_Laere_syndrome_2|Inborn_genetic_diseases": 32,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2": 16,
    "not_provided|Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2": 6,
    "Brown-Vialetto-van_Laere_syndrome_2|not_provided": 13,
    "Auditory_neuropathy_spectrum_disorder|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "SLC52A2-related_disorder|Brown-Vialetto-van_Laere_syndrome_2": 3,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2|not_provided": 5,
    "Brown-Vialetto-van_Laere_syndrome_2|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Brown-Vialetto-van_Laere_syndrome_2|not_provided|SLC52A2-related_disorder": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|not_specified|Inborn_genetic_diseases|SLC52A2-related_disorder": 1,
    "SLC52A2-related_disorder|Brown-Vialetto-van_Laere_syndrome_2|Mitochondrial_disease": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_2|Inborn_genetic_diseases": 4,
    "Brown-Vialetto-van_Laere_syndrome_2|SLC52A2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|not_specified|not_provided": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|Inborn_genetic_diseases|not_specified": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|not_specified": 2,
    "not_specified|Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2": 3,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_1|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "not_specified|Brown-Vialetto-van_Laere_syndrome_2": 2,
    "SLC52A2-related_disorder|not_provided|Brown-Vialetto-van_Laere_syndrome_2|Inborn_genetic_diseases": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|SLC52A2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Brown-Vialetto-van_Laere_syndrome_2|Mitochondrial_disease": 1,
    "not_provided|Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2|SLC52A2-related_disorder": 1,
    "Sensorineural_hearing_loss_disorder|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "SLC52A2-related_disorder|Inborn_genetic_diseases|not_provided|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|not_specified|not_provided|SLC52A2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "SLC52A2-related_disorder": 1,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2|not_specified|not_provided|SLC52A2-related_disorder": 1,
    "Inborn_genetic_diseases|SLC52A2-related_disorder|not_provided|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_2": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_2|not_specified": 1,
    "not_specified|Brown-Vialetto-van_Laere_syndrome_2|Inborn_genetic_diseases": 1,
    "Brown-Vialetto-van_Laere_syndrome_2|Brown-Vialetto-van_Laere_syndrome_1": 1,
    "Myopia_27": 13,
    "CPSF1-related_disorder": 10,
    "Myopia_27|not_provided": 1,
    "CPSF1-related_disorder|not_specified": 1,
    "not_specified|Myopia_27": 1,
    "Hereditary_acrodermatitis_enteropathica": 109,
    "Hereditary_acrodermatitis_enteropathica|not_provided": 47,
    "Hereditary_acrodermatitis_enteropathica|Inborn_genetic_diseases": 6,
    "not_provided|Hereditary_acrodermatitis_enteropathica": 54,
    "SLC39A4-related_disorder|not_provided|Hereditary_acrodermatitis_enteropathica": 2,
    "SLC39A4-related_disorder|not_provided": 5,
    "Hereditary_acrodermatitis_enteropathica|not_provided|SLC39A4-related_disorder": 3,
    "not_provided|SLC39A4-related_disorder": 5,
    "not_provided|SLC39A4-related_disorder|Hereditary_acrodermatitis_enteropathica|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_acrodermatitis_enteropathica|SLC39A4-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SLC39A4-related_disorder": 1,
    "not_specified|not_provided|Hereditary_acrodermatitis_enteropathica": 5,
    "not_provided|Hereditary_acrodermatitis_enteropathica|SLC39A4-related_disorder": 3,
    "Inborn_genetic_diseases|Hereditary_acrodermatitis_enteropathica|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_acrodermatitis_enteropathica": 2,
    "not_provided|not_specified|Hereditary_acrodermatitis_enteropathica": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_acrodermatitis_enteropathica": 1,
    "Hereditary_acrodermatitis_enteropathica|SLC39A4-related_disorder|not_provided": 1,
    "not_provided|SLC39A4-related_disorder|Hereditary_acrodermatitis_enteropathica": 1,
    "SLC39A4-related_disorder": 2,
    "Hereditary_acrodermatitis_enteropathica|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Sponastrime_dysplasia": 1,
    "Sponastrime_dysplasia": 26,
    "TONSL-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TONSL-related_disorder": 20,
    "TONSL-related_disorder|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|TONSL-related_disorder": 2,
    "not_provided|Sponastrime_dysplasia": 16,
    "not_provided|Sponastrime_dysplasia|Inborn_genetic_diseases": 2,
    "TONSL-related_disorder": 5,
    "Sponastrime_dysplasia|not_provided": 6,
    "TONSL-related_disorder|Sponastrime_dysplasia|not_provided": 1,
    "not_provided|TONSL-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|TONSL-related_disorder|Sponastrime_dysplasia": 1,
    "Sponastrime_dysplasia|not_provided|Inborn_genetic_diseases": 1,
    "Skeletal_dysplaisia_with_extra-skeletal_manifestations": 1,
    "Skeletal_dysplaisia_with_extra-skeletal_manifestations|not_provided": 1,
    "Skeletal_dysplaisia_with_extra-skeletal_manifestations|TONSL-related_disorder": 2,
    "Spondylometaphyseal_dysplasia|Sponastrime_dysplasia|not_provided": 1,
    "Inborn_genetic_diseases|TONSL-related_disorder|not_provided|Sponastrime_dysplasia": 1,
    "Skeletal_dysplaisia_with_extra-skeletal_manifestations|TONSL-related_disorder|Sponastrime_dysplasia": 1,
    "Inborn_genetic_diseases|not_provided|TONSL-related_disorder": 1,
    "not_provided|Skeletal_dysplaisia_with_extra-skeletal_manifestations|TONSL-related_disorder|Sponastrime_dysplasia": 1,
    "Sponastrime_dysplasia|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_gross_motor_and_speech_delay": 6,
    "CBL-related_disorder": 185,
    "not_provided|Holoprosencephaly_sequence|not_specified": 1,
    "not_provided|not_specified|Holoprosencephaly_sequence": 2,
    "Holoprosencephaly_sequence|Inborn_genetic_diseases": 7,
    "not_specified|Holoprosencephaly_sequence|FOXH1-related_disorder": 1,
    "not_specified|not_provided|Holoprosencephaly_sequence": 6,
    "Inborn_genetic_diseases|Holoprosencephaly_sequence": 8,
    "FOXH1-related_disorder": 5,
    "FOXH1-related_disorder|Holoprosencephaly_sequence": 1,
    "Inborn_genetic_diseases|FOXH1-related_disorder": 1,
    "Holoprosencephaly_sequence|not_provided|not_specified": 4,
    "not_provided|FOXH1-related_disorder": 1,
    "Holoprosencephaly_sequence|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Holoprosencephaly_sequence": 1,
    "Holoprosencephaly_sequence|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Holoprosencephaly_sequence|Inborn_genetic_diseases": 1,
    "Conotruncal_defect": 6,
    "Holoprosencephaly_sequence|FOXH1-related_disorder": 1,
    "FOXH1-related_disorder|Holoprosencephaly_sequence|Inborn_genetic_diseases": 1,
    "not_provided|Conotruncal_defect": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_sequence|not_provided": 1,
    "FOXH1-related_disorder|not_provided": 1,
    "GPT_POLYMORPHISM": 1,
    "RECQL4-related_disorder": 4,
    "Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome": 17,
    "Baller-Gerold_syndrome": 3068,
    "not_specified|not_provided|Baller-Gerold_syndrome|RECQL4-related_disorder": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases": 462,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Baller-Gerold_syndrome": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome": 519,
    "Rapadilino_syndrome": 5,
    "RECQL4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome": 3,
    "not_provided|Baller-Gerold_syndrome": 62,
    "not_specified|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 1,
    "not_provided|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome": 17,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|not_provided": 48,
    "not_provided|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 1,
    "RECQL4-related_disorder|not_provided|Baller-Gerold_syndrome": 2,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome": 3,
    "Baller-Gerold_syndrome|not_specified": 13,
    "RECQL4-related_disorder|Baller-Gerold_syndrome": 15,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome": 6,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 10,
    "not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 21,
    "Baller-Gerold_syndrome|RECQL4-related_disorder|not_provided": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|RECQL4-related_disorder|Baller-Gerold_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome": 5,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 1,
    "not_specified|Baller-Gerold_syndrome": 5,
    "Baller-Gerold_syndrome|not_provided|not_specified": 3,
    "Rapadilino_syndrome|not_specified|not_provided|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 2,
    "not_provided|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 2,
    "Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|RECQL4-related_disorder": 7,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 3,
    "Baller-Gerold_syndrome|not_specified|Inborn_genetic_diseases": 2,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Ovarian_cancer": 1,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2": 1,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|not_specified": 1,
    "Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 2,
    "not_provided|Baller-Gerold_syndrome|Inborn_genetic_diseases": 6,
    "Rothmund-Thomson_syndrome": 2,
    "Baller-Gerold_syndrome|RECQL4-related_disorder": 27,
    "Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 16,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Ovarian_cancer|not_specified|not_provided|Baller-Gerold_syndrome": 1,
    "Absent_radius|Baller-Gerold_syndrome": 1,
    "Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Baller-Gerold_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Baller-Gerold_syndrome": 8,
    "RECQL4-related_disorder|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Baller-Gerold_syndrome|Ovarian_cancer": 4,
    "not_provided|Baller-Gerold_syndrome|RECQL4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Ovarian_cancer|RECQL4-related_disorder|not_specified": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|Rothmund-Thomson_syndrome|Rapadilino_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
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    "Baller-Gerold_syndrome|Multiple_myeloma": 1,
    "Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|Ehlers-Danlos_syndrome": 2,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_specified|not_provided": 2,
    "Rothmund-Thomson_syndrome_type_2|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "not_provided|Congenital_heart_disease|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome": 2,
    "Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder|Baller-Gerold_syndrome": 2,
    "Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Baller-Gerold_syndrome": 2,
    "not_specified|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|RECQL4-related_disorder|not_provided|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome": 4,
    "Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 4,
    "RECQL4-related_disorder|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Rothmund-Thomson_syndrome_type_2|not_provided|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder": 2,
    "not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome|RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|not_specified": 1,
    "Baller-Gerold_syndrome|RECQL4-related_disorder|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 1,
    "not_provided|Baller-Gerold_syndrome|RECQL4-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|not_provided": 4,
    "Baller-Gerold_syndrome|RECQL4-related_disorder|Inborn_genetic_diseases": 5,
    "Ovarian_cancer|Baller-Gerold_syndrome": 3,
    "Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2": 1,
    "Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome|Ovarian_cancer": 1,
    "Rapadilino_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 1,
    "RECQL4-related_spectrum_disorders|not_provided|Baller-Gerold_syndrome": 1,
    "not_provided|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 2,
    "Rothmund-Thomson_syndrome_type_2|not_provided|RECQL4-related_disorder|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|not_provided|Inborn_genetic_diseases": 7,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Ovarian_cancer|not_provided|Malignant_tumor_of_breast|Baller-Gerold_syndrome|RECQL4-related_disorder": 1,
    "RECQL4-related_disorder|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Baller-Gerold_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome": 1,
    "Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|RECQL4-related_disorder|Baller-Gerold_syndrome": 1,
    "RECQL4-related_disorder|Inborn_genetic_diseases": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 2,
    "Baller-Gerold_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "RECQL4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_specified": 1,
    "Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome": 4,
    "not_provided|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Ovarian_cancer|not_specified|Baller-Gerold_syndrome|not_provided": 1,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome|not_specified|RECQL4-related_disorder|not_provided|Rothmund-Thomson_syndrome_type_2": 1,
    "Rothmund-Thomson_syndrome_type_2|not_provided|Baller-Gerold_syndrome": 5,
    "Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Baller-Gerold_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 2,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Rapadilino_syndrome|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|RECQL4-related_disorder": 1,
    "not_specified|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Inborn_genetic_diseases": 7,
    "Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 2,
    "Baller-Gerold_syndrome|not_specified|not_provided": 1,
    "Rothmund-Thomson_syndrome|Rapadilino_syndrome|Baller-Gerold_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome|not_provided": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 2,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|not_provided": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Inborn_genetic_diseases": 5,
    "Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Baller-Gerold_syndrome|RECQL4-related_disorder|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Baller-Gerold_syndrome": 13,
    "not_provided|Baller-Gerold_syndrome|Inborn_genetic_diseases|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases": 4,
    "RECQL4-related_disorder|not_specified|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|Rapadilino_syndrome": 1,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|not_provided|Baller-Gerold_syndrome": 1,
    "Inborn_genetic_diseases|RECQL4-related_disorder|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Rapadilino_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|not_provided": 10,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|RECQL4-related_disorder": 1,
    "not_provided|RECQL4-related_disorder|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|RECQL4-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|not_provided|RECQL4-related_disorder": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "not_provided|RECQL4-related_disorder|Inborn_genetic_diseases|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Rapadilino_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome|Inborn_genetic_diseases": 3,
    "RECQL4-related_disorder|Inborn_genetic_diseases|Baller-Gerold_syndrome": 6,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 2,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2": 3,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_cancer|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Inborn_genetic_diseases|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Inborn_genetic_diseases": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|RECQL4-related_disorder": 3,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases": 5,
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    "Rothmund-Thomson_syndrome|Rapadilino_syndrome|Baller-Gerold_syndrome|Inborn_genetic_diseases": 1,
    "Rapadilino_syndrome|RECQL4-related_disorder|Baller-Gerold_syndrome|not_provided": 1,
    "Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|Baller-Gerold_syndrome": 3,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Familial_meningioma|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome|Baller-Gerold_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Rapadilino_syndrome|Rothmund-Thomson_syndrome": 3,
    "Baller-Gerold_syndrome|not_provided|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Baller-Gerold_syndrome|not_specified|RECQL4-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome|Baller-Gerold_syndrome|Rapadilino_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Rapadilino_syndrome|not_provided|Inborn_genetic_diseases|Baller-Gerold_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome": 1,
    "not_specified|Baller-Gerold_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome": 5,
    "RECQL4-related_disorder|Baller-Gerold_syndrome|Ovarian_cancer": 1,
    "Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder|not_provided|Baller-Gerold_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|not_provided": 11,
    "Hereditary_cancer-predisposing_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|Baller-Gerold_syndrome": 1,
    "not_specified|not_provided|Baller-Gerold_syndrome": 1,
    "Malignant_fibrous_histiocytoma|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|not_provided": 1,
    "not_specified|Baller-Gerold_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome": 1,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome": 5,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Inborn_genetic_diseases|Rapadilino_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|not_specified": 2,
    "not_specified|RECQL4-related_disorder|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome": 1,
    "RECQL4-related_disorder|Baller-Gerold_syndrome|Inborn_genetic_diseases": 3,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|not_specified|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|not_provided|RECQL4-related_disorder": 1,
    "Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|Rapadilino_syndrome|Baller-Gerold_syndrome|not_specified|not_provided": 1,
    "Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Baller-Gerold_syndrome|RECQL4-related_disorder|High_grade_surface_osteosarcoma|B_lymphoblastic_leukemia_lymphoma_with_t(12%3B21)(p13%3Bq22)%3B_TEL-AML1_(ETV6-RUNX1)|Inborn_genetic_diseases|not_provided|Rothmund-Thomson_syndrome": 1,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|not_provided|Baller-Gerold_syndrome": 1,
    "RECQL4-related_disorder|Inborn_genetic_diseases|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|not_specified|not_provided": 1,
    "Baller-Gerold_syndrome|not_provided|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|RECQL4-related_disorder|not_specified|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Baller-Gerold_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Baller-Gerold_syndrome": 1,
    "not_provided|Rothmund-Thomson_syndrome_type_2": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_specified": 1,
    "Baller-Gerold_syndrome|RECQL4-related_spectrum_disorders": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome": 2,
    "not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "not_specified|Baller-Gerold_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "RECQL4-related_disorder|Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rothmund-Thomson_syndrome|Ovarian_cancer|not_provided": 1,
    "Inborn_genetic_diseases|RECQL4-related_disorder": 1,
    "RECQL4-related_disorder|Ovarian_cancer|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|not_provided|not_specified|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 2,
    "not_provided|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome|not_specified|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 2,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|RECQL4-related_disorder|not_specified|not_provided": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome|not_provided|not_specified": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome": 2,
    "Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Baller-Gerold_syndrome|Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2": 1,
    "not_specified|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder": 1,
    "Hepatoblastoma|Baller-Gerold_syndrome": 1,
    "Rapadilino_syndrome|not_specified|Baller-Gerold_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome|RECQL4-related_disorder|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Baller-Gerold_syndrome|RECQL4-related_disorder": 1,
    "RECQL4-related_disorder|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Baller-Gerold_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|RECQL4-related_disorder|Baller-Gerold_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Baller-Gerold_syndrome|not_specified|RECQL4-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|RECQL4-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Baller-Gerold_syndrome": 3,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Baller-Gerold_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|not_provided": 1,
    "RECQL4-related_disorder|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2|not_specified": 1,
    "not_specified|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Ovarian_cancer": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Ovarian_cancer|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "RECQL4-related_disorder|not_provided|Inborn_genetic_diseases|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Baller-Gerold_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Baller-Gerold_syndrome": 1,
    "RECQL4-related_disorder|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Baller-Gerold_syndrome|Rapadilino_syndrome": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 1,
    "Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Rapadilino_syndrome|Baller-Gerold_syndrome": 1,
    "Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome|Inborn_genetic_diseases": 1,
    "Baller-Gerold_syndrome|RECQL4-related_disorder|not_specified": 1,
    "RECQL4-related_disorder|Baller-Gerold_syndrome|not_provided": 1,
    "Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Inborn_genetic_diseases|not_provided|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|not_specified|Baller-Gerold_syndrome|Rapadilino_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Rapadilino_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Rapadilino_syndrome|RECQL4-related_disorder": 1,
    "Baller-Gerold_syndrome|not_provided|Inborn_genetic_diseases|RECQL4-related_disorder": 1,
    "RECQL4-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Baller-Gerold_syndrome": 1,
    "Inborn_genetic_diseases|Rothmund-Thomson_syndrome_type_2|not_specified|not_provided|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|not_provided|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|RECQL4-related_disorder|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Inborn_genetic_diseases|RECQL4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Baller-Gerold_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|RECQL4-related_disorder|not_provided|Baller-Gerold_syndrome": 1,
    "Rapadilino_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_heart_disease|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome|Baller-Gerold_syndrome": 1,
    "not_provided|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|Ovarian_cancer": 1,
    "RECQL4-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Baller-Gerold_syndrome": 2,
    "Baller-Gerold_syndrome|not_specified|Rothmund-Thomson_syndrome_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Rapadilino_syndrome": 1,
    "not_provided|Baller-Gerold_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "RECQL4-related_disorder|Inborn_genetic_diseases|not_specified|Baller-Gerold_syndrome": 1,
    "Rothmund-Thomson_syndrome_type_2|Baller-Gerold_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2": 1,
    "Rothmund-Thomson_syndrome_type_2|Inborn_genetic_diseases|Baller-Gerold_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Baller-Gerold_syndrome|not_provided|Rothmund-Thomson_syndrome_type_2|Rapadilino_syndrome|Rothmund-Thomson_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Baller-Gerold_syndrome|not_provided": 1,
    "Baller-Gerold_syndrome|Rothmund-Thomson_syndrome_type_2|not_provided": 1,
    "not_specified|not_provided|Hyper-IgE_syndrome": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency": 207,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided": 12,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|.": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Inborn_genetic_diseases": 20,
    ".|DOCK8-related_disorder|not_provided|not_specified": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 11,
    ".|DOCK8-related_disorder": 11,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases": 11,
    "DOCK8-related_disorder": 16,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 53,
    ".|Inborn_genetic_diseases|not_provided": 3,
    ".|Combined_immunodeficiency_due_to_DOCK8_deficiency": 34,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_provided": 3,
    ".|DOCK8-related_disorder|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|Intellectual_disability": 1,
    ".|not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 2,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency": 11,
    "Severe_combined_immunodeficiency_disease|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided": 1,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|.|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified": 7,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 5,
    "not_specified|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Inborn_genetic_diseases|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 5,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 8,
    ".|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|not_provided": 5,
    ".|DOCK8-related_disorder|not_specified": 4,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_specified": 5,
    "not_provided|.|DOCK8-related_disorder|not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 1,
    "not_provided|.|not_specified|Hyper-IgE_syndrome": 1,
    "not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency": 5,
    "DOCK8-related_disorder|not_specified|.|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    ".|DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided": 1,
    "not_provided|.|Combined_immunodeficiency_due_to_DOCK8_deficiency": 6,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_specified|not_provided": 2,
    ".|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 4,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Inborn_genetic_diseases|.": 2,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 16,
    "not_provided|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "DOCK8-related_disorder|.": 7,
    "not_provided|.|DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 2,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|DOCK8-related_disorder|not_specified": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|DOCK8-related_disorder|not_provided": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided|not_specified|.": 6,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified": 3,
    "DOCK8-related_disorder|not_provided|not_specified|.|Hyper-IgE_syndrome": 1,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 3,
    "not_specified|.|not_provided": 2,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|not_provided": 6,
    "not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided|.": 2,
    "DOCK8-related_disorder|not_specified": 1,
    "not_specified|.|Inborn_genetic_diseases": 2,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided": 6,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided|.": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    ".|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified": 2,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Hepatoblastoma": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    "not_specified|not_provided|.|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "not_provided|.|Inborn_genetic_diseases": 3,
    "DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    "Severe_combined_immunodeficiency_disease|.": 1,
    ".|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 2,
    "Intellectual_disability|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 4,
    ".|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency": 3,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|DOCK8-related_disorder": 1,
    "Hyper-IgE_syndrome": 9,
    "Hepatoblastoma|.": 1,
    "not_provided|.|DOCK8-related_disorder|not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    ".|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided": 2,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 1,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 4,
    ".|Intellectual_disability|_autosomal_dominant_2": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|DOCK8-related_disorder|not_provided": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|not_provided|.": 5,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Combined_immunodeficiency_due_to_DOCK8_deficiency": 3,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|DOCK8-related_disorder|not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "not_specified|not_provided|Intellectual_disability|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "not_provided|not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 3,
    "not_provided|.|not_specified": 6,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_specified": 2,
    "Inborn_genetic_diseases|DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "not_provided|DOCK8-related_disorder|.": 1,
    ".|Inborn_genetic_diseases|DOCK8-related_disorder": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    ".|DOCK8-related_disorder|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 1,
    "not_provided|.|not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "not_specified|Inborn_genetic_diseases|.|not_provided": 1,
    "not_provided|.|DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_provided|not_specified": 1,
    "DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency": 3,
    "DOCK8-related_disorder|.|not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    ".|Hyper-IgE_syndrome": 1,
    "not_specified|not_provided|.|Hyper-IgE_syndrome": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Inborn_genetic_diseases|not_specified": 1,
    ".|Combined_immunodeficiency_due_to_DOCK8_deficiency|DOCK8-related_disorder": 1,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_specified": 1,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 2,
    "DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 2,
    "DOCK8-related_disorder|.|not_specified": 2,
    "DOCK8-related_disorder|.|not_specified|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_specified": 1,
    ".|Inborn_genetic_diseases|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_provided|DOCK8-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|.": 1,
    "Intellectual_disability|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    ".|not_provided|DOCK8-related_disorder": 2,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided|Inborn_genetic_diseases|.": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Hepatoblastoma": 1,
    ".|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided|not_specified": 1,
    "not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_provided": 5,
    "not_provided|DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|.|Inborn_genetic_diseases": 1,
    "DOCK8-related_disorder|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|not_provided|.": 1,
    "not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|.|not_provided": 1,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_specified|.|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|Inborn_genetic_diseases|Hyper-IgE_syndrome": 1,
    "not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|.|DOCK8-related_disorder": 1,
    "not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency|.": 1,
    "Inborn_genetic_diseases|not_provided|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|.": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|.": 2,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided|Combined_immunodeficiency_due_to_DOCK8_deficiency|Intellectual_disability": 1,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|not_specified|.|not_provided": 2,
    "Combined_immunodeficiency_due_to_DOCK8_deficiency|DOCK8-related_disorder|Inborn_genetic_diseases": 1,
    ".|not_provided|not_specified|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "Intellectual_disability|_autosomal_dominant_2|.": 1,
    "KANK1-related_disorder": 19,
    "not_provided|Cerebral_palsy|_spastic_quadriplegic|_2": 24,
    "Cerebral_palsy|_spastic_quadriplegic|_2|not_provided": 23,
    "not_provided|KANK1-related_disorder": 13,
    "Cerebral_palsy|_spastic_quadriplegic|_2": 14,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "not_specified|not_provided|Cerebral_palsy|_spastic_quadriplegic|_2": 7,
    "Cerebral_palsy|_spastic_quadriplegic|_2|not_provided|not_specified": 4,
    "not_provided|not_specified|Cerebral_palsy|_spastic_quadriplegic|_2": 7,
    "KANK1-related_disorder|not_specified": 2,
    "not_provided|KANK1-related_disorder|not_specified": 1,
    "KANK1-related_disorder|not_provided": 14,
    "Cerebral_palsy|_spastic_quadriplegic|_2|KANK1-related_disorder|not_provided": 1,
    "KANK1-related_disorder|Cerebral_palsy|_spastic_quadriplegic|_2|not_provided": 3,
    "not_provided|not_specified|KANK1-related_disorder": 3,
    "not_specified|Cerebral_palsy|_spastic_quadriplegic|_2|not_provided": 5,
    "not_provided|KANK1-related_disorder|Cerebral_palsy|_spastic_quadriplegic|_2": 2,
    "KANK1-related_disorder|not_provided|Cerebral_palsy|_spastic_quadriplegic|_2": 4,
    "Cerebral_palsy|_spastic_quadriplegic|_2|not_specified|not_provided": 6,
    "not_specified|Cerebral_palsy|_spastic_quadriplegic|_2": 3,
    "not_provided|Cerebral_palsy|_spastic_quadriplegic|_2|KANK1-related_disorder": 2,
    "KANK1-related_disorder|not_specified|not_provided": 2,
    "not_specified|KANK1-related_disorder|not_provided": 2,
    "not_provided|Cerebral_palsy|_spastic_quadriplegic|_2|not_specified": 1,
    "Cerebral_palsy|_spastic_quadriplegic|_2|not_provided|KANK1-related_disorder": 3,
    "KANK1-related_disorder|not_provided|not_specified": 1,
    "KANK1-related_disorder|Rare_genetic_intellectual_disability|not_provided": 1,
    "46|XY_sex_reversal_4": 1,
    "Gonadal_agenesis": 1,
    "DMRT2-related_disorder|not_provided": 4,
    "DMRT2-related_disorder": 8,
    "not_provided|DMRT2-related_disorder": 2,
    "not_specified|DMRT2-related_disorder": 1,
    "Nicolaides-Baraitser_syndrome": 113,
    "Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome": 2,
    "not_specified|Nicolaides-Baraitser_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Nicolaides-Baraitser_syndrome|not_provided": 28,
    "Blepharophimosis-impaired_intellectual_development_syndrome|Nicolaides-Baraitser_syndrome|not_provided": 1,
    "not_provided|SMARCA2-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases|SMARCA2-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome": 3,
    "Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "SMARCA2-related_disorder": 21,
    "SMARCA2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome": 3,
    "SMARCA2-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Nicolaides-Baraitser_syndrome|not_provided|Blepharophimosis-impaired_intellectual_development_syndrome|SMARCA2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Nicolaides-Baraitser_syndrome": 24,
    "Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome": 2,
    "SMARCA2-related_disorder|Inborn_genetic_diseases|Coffin_Siris/Intellectual_Disability|not_provided": 1,
    "SMARCA2-related_disorder|not_provided": 7,
    "not_provided|Inborn_genetic_diseases|not_specified|Nicolaides-Baraitser_syndrome": 1,
    "Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome|Inborn_genetic_diseases": 1,
    "Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Coffin_Siris/Intellectual_Disability|Nicolaides-Baraitser_syndrome": 1,
    "not_provided|not_specified|Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Nicolaides-Baraitser_syndrome": 2,
    "not_provided|Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases": 3,
    "Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases|Blepharophimosis-impaired_intellectual_development_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Nicolaides-Baraitser_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Nicolaides-Baraitser_syndrome": 6,
    "Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome|not_specified|not_provided": 1,
    "Nicolaides-Baraitser_syndrome|not_provided|SMARCA2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SMARCA2-related_disorder|not_provided": 1,
    "Nicolaides-Baraitser_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|SMARCA2-related_disorder": 4,
    "SMARCA2-related_disorder|Inborn_genetic_diseases": 1,
    "Nicolaides-Baraitser_syndrome|Coffin-Siris_syndrome_1|not_provided": 1,
    "Blepharophimosis-impaired_intellectual_development_syndrome|not_provided|Nicolaides-Baraitser_syndrome": 3,
    "Blepharophimosis-impaired_intellectual_development_syndrome": 6,
    "not_provided|SMARCA2-related_disorder|Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome": 1,
    "Severe_intellectual_deficiency|Intellectual_disability": 1,
    "not_provided|SMARCA2-related_disorder": 7,
    "Intellectual_disability|Blepharophimosis-impaired_intellectual_development_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome": 2,
    "Intellectual_disability|Blepharophimosis": 1,
    "Nicolaides-Baraitser_syndrome|SMARCA2-related_disorder": 1,
    "Intellectual_disability|not_provided|Blepharophimosis-impaired_intellectual_development_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|Blepharophimosis-impaired_intellectual_development_syndrome": 1,
    "Intellectual_disability|Nicolaides-Baraitser_syndrome": 2,
    "Nicolaides-Baraitser_syndrome|not_provided|SMARCA2-related_disorder": 2,
    "Nicolaides-Baraitser_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SMARCA2-related_disorder|Nicolaides-Baraitser_syndrome": 1,
    "Chiari_malformation": 1,
    "Nicolaides-Baraitser_syndrome|SMARCA2-related_BAFopathy": 1,
    "not_provided|SMARCA2-related_BAFopathy|Nicolaides-Baraitser_syndrome": 1,
    "SMARCA2-related_BAFopathy|not_provided|Nicolaides-Baraitser_syndrome": 3,
    "SMARCA2-related_BAFopathy|Nicolaides-Baraitser_syndrome": 1,
    "Blepharophimosis-impaired_intellectual_development_syndrome|not_provided": 1,
    "SMARCA2-related_BAFopathy": 1,
    "not_provided|Nicolaides-Baraitser_syndrome|Coffin-Siris_syndrome": 1,
    "not_provided|SMARCA2-related_BAFopathy": 1,
    "not_provided|Nicolaides-Baraitser_syndrome|SMARCA2-related_disorder": 1,
    "Blepharophimosis-impaired_intellectual_development_syndrome|Intellectual_disability": 1,
    "Intellectual_disability|Blepharophimosis-impaired_intellectual_development_syndrome": 2,
    "SMARCA2-related_BAFopathy|Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome|not_provided|Intellectual_disability": 1,
    "Blepharophimosis-impaired_intellectual_development_syndrome|Nicolaides-Baraitser_syndrome": 3,
    "Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Blepharophimosis-impaired_intellectual_development_syndrome|Nicolaides-Baraitser_syndrome": 2,
    "Nicolaides-Baraitser_syndrome|Intellectual_disability|Hirsutism|not_provided": 1,
    "Nicolaides-Baraitser_syndrome|not_provided|Inborn_genetic_diseases|SMARCA2-related_disorder": 1,
    "SMARCA2-related_disorder|not_provided|Nicolaides-Baraitser_syndrome": 1,
    "Inborn_genetic_diseases|SMARCA2-related_disorder|not_provided|Nicolaides-Baraitser_syndrome": 2,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_provided|Nicolaides-Baraitser_syndrome": 1,
    "not_provided|Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome": 3,
    "Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Nicolaides-Baraitser_syndrome|SMARCA2-related_disorder|Inborn_genetic_diseases": 1,
    "Nicolaides-Baraitser_syndrome|not_provided|Blepharophimosis-impaired_intellectual_development_syndrome": 1,
    "SMARCA2-related_disorder|not_specified": 1,
    "not_provided|not_specified|Nicolaides-Baraitser_syndrome|Inborn_genetic_diseases": 1,
    "Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|SMARCA2-related_disorder|not_specified|Nicolaides-Baraitser_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome|Blepharophimosis-impaired_intellectual_development_syndrome": 1,
    "Inborn_genetic_diseases|Nicolaides-Baraitser_syndrome|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_provided": 2,
    "Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 3,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 55,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia|not_provided": 9,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 13,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia": 9,
    "not_specified|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "not_provided|Congenital_cerebellar_hypoplasia|not_specified": 1,
    "VLDLR-related_disorder": 1,
    "VLDLR-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified|not_provided": 1,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified|Congenital_cerebellar_hypoplasia": 1,
    "not_specified|not_provided|Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 6,
    "VLDLR-related_disorder|not_provided": 3,
    "not_provided|not_specified|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Inborn_genetic_diseases": 2,
    "VLDLR-related_disorder|not_provided|not_specified": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "not_specified|not_provided|VLDLR-related_disorder": 1,
    "Congenital_cerebellar_hypoplasia|not_specified|not_provided": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia|VLDLR-related_disorder|not_provided": 1,
    "not_provided|Congenital_cerebellar_hypoplasia|Dysequilibrium_syndrome|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_provided": 1,
    "not_provided|Congenital_cerebellar_hypoplasia|not_specified|Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified": 2,
    "not_provided|VLDLR-related_disorder": 2,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_provided": 5,
    "Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia": 2,
    "VLDLR-related_disorder|not_specified|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Intellectual_disability": 1,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|VLDLR-related_disorder": 3,
    "not_provided|Congenital_cerebellar_hypoplasia": 1,
    "not_specified|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "not_provided|not_specified|VLDLR-related_disorder": 1,
    "VLDLR-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_provided": 1,
    "not_specified|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_provided": 2,
    "not_provided|VLDLR-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "not_provided|not_specified|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia": 1,
    "Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "not_specified|VLDLR-related_disorder|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|VLDLR-related_disorder|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "VLDLR-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "not_specified|Congenital_cerebellar_hypoplasia|VLDLR-related_disorder|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "See_cases|Inborn_genetic_diseases|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Dysequilibrium_syndrome": 2,
    "not_provided|Congenital_cerebellar_hypoplasia|Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "VLDLR-related_disorder|not_specified|not_provided|Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_provided|Congenital_cerebellar_hypoplasia|not_specified": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Cerebellar_hypoplasia": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "VLDLR-related_disorder|not_specified|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1": 1,
    "Inborn_genetic_diseases|Congenital_cerebellar_hypoplasia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_1|not_specified": 1,
    "Cone_dystrophy_with_supernormal_rod_response": 41,
    "not_provided|Cone_dystrophy_with_supernormal_rod_response": 26,
    "Cone_dystrophy_with_supernormal_rod_response|not_provided": 12,
    "KCNV2-related_disorder|not_provided": 4,
    "not_provided|Retinal_dystrophy|Cone_dystrophy_with_supernormal_rod_response": 1,
    "Cone_dystrophy_with_supernormal_rod_response|Inborn_genetic_diseases|not_provided": 2,
    "Optic_atrophy|Inborn_genetic_diseases|KCNV2-related_disorder|Retinal_dystrophy|not_provided|Cone_dystrophy_with_supernormal_rod_response": 1,
    "not_specified|not_provided|KCNV2-related_disorder": 1,
    "KCNV2-related_disorder|Retinal_dystrophy|not_provided|Cone_dystrophy_3|Cone_dystrophy_with_supernormal_rod_response": 1,
    "KCNV2-related_disorder|Cone_dystrophy_with_supernormal_rod_response|not_provided": 2,
    "not_provided|Cone_dystrophy_with_supernormal_rod_response|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Cone_dystrophy_with_supernormal_rod_response": 9,
    "Inborn_genetic_diseases|not_provided|Cone_dystrophy_with_supernormal_rod_response|Retinal_dystrophy": 1,
    "KCNV2-related_disorder|not_provided|Cone_dystrophy_with_supernormal_rod_response": 2,
    "not_provided|KCNV2-related_disorder": 3,
    "not_provided|Cone_dystrophy_with_supernormal_rod_response|Retinal_dystrophy": 1,
    "Progressive_cone_dystrophy_(without_rod_involvement)|Stargardt_disease|Cone_dystrophy_with_supernormal_rod_response": 1,
    "cone_dystrophy_with_supernormal_rod_electroretinogram": 5,
    "Cone_dystrophy|Cone_dystrophy_with_supernormal_rod_response": 1,
    "KCNV2-related_disorder|Retinal_dystrophy|not_provided|Cone_dystrophy_with_supernormal_rod_response": 1,
    "Retinal_dystrophy|KCNV2-related_disorder": 1,
    "not_provided|KCNV2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cone_dystrophy_with_supernormal_rod_response": 3,
    "KCNV2-related_disorder|not_specified|not_provided|Cone_dystrophy_with_supernormal_rod_response": 2,
    "KCNV2-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Cone_dystrophy_with_supernormal_rod_response|not_provided": 1,
    "Retinal_dystrophy|Cone_dystrophy|not_provided": 1,
    "cone_dystrophy_with_supernormal_rod_electroretinogram|not_provided": 2,
    "not_provided|not_specified|Cone_dystrophy_with_supernormal_rod_response": 4,
    "not_provided|Cone_dystrophy_with_supernormal_rod_response|not_specified": 1,
    "not_provided|not_specified|KCNV2-related_disorder": 1,
    "Cone-rod_dystrophy_6": 6,
    "cone_dystrophy_with_supernormal_rod_electroretinogram|not_provided|Cone_dystrophy_with_supernormal_rod_response": 1,
    "not_provided|KCNV2-related_disorder|Cone_dystrophy_with_supernormal_rod_response": 1,
    "Retinal_dystrophy|Cone_dystrophy_with_supernormal_rod_response|not_provided": 1,
    "Inborn_genetic_diseases|Cone_dystrophy_with_supernormal_rod_response|Retinal_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cone_dystrophy_with_supernormal_rod_response": 1,
    "Inborn_genetic_diseases|KCNV2-related_disorder": 1,
    "Cone_dystrophy|Retinal_dystrophy": 1,
    "KCNV2-related_disorder|Retinal_dystrophy|not_provided|Nystagmus|Abnormality_of_the_nervous_system|Cone_dystrophy_with_supernormal_rod_response": 1,
    "not_provided|KCNV2-related_disorder|Retinal_dystrophy": 1,
    "KCNV2-related_disorder": 1,
    "RFX3-related_disorder": 14,
    "RFX3-related_disorder|not_provided": 4,
    "not_provided|RFX3-related_disorder": 1,
    "RFX3-related_intellectual_disability|not_provided": 1,
    "RFX3-associated_neurodevelopmental_disorder": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 283,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_provided": 23,
    "not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 62,
    "GLIS3-related_disorder": 4,
    "Congenital_aniridia|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "not_provided|GLIS3-related_disorder|Monogenic_diabetes|not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Inborn_genetic_diseases": 15,
    "Inborn_genetic_diseases|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 9,
    "not_provided|GLIS3-related_disorder|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 2,
    "GLIS3-related_disorder|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_specified": 1,
    "Inborn_genetic_diseases|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Monogenic_diabetes|not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes": 1,
    "Monogenic_diabetes|Inborn_genetic_diseases|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "not_specified|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 4,
    "not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|GLIS3-related_disorder": 2,
    "not_provided|not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Diabetes_mellitus|Monogenic_diabetes|not_specified|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "not_provided|GLIS3-related_disorder": 2,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_specified": 2,
    "Diabetes_mellitus|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_specified": 1,
    "Monogenic_diabetes|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 2,
    "Transitory_neonatal_diabetes_mellitus": 3,
    "Inborn_genetic_diseases|Monogenic_diabetes|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Inborn_genetic_diseases": 1,
    "not_provided|GLIS3-related_disorder|Transitory_neonatal_diabetes_mellitus|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 2,
    "Monogenic_diabetes|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 2,
    "Monogenic_diabetes|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|GLIS3-related_disorder": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes": 1,
    "not_provided|not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|GLIS3-related_disorder": 1,
    "not_provided|GLIS3-related_disorder|Monogenic_diabetes|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Transitory_neonatal_diabetes_mellitus|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes|not_provided": 1,
    "not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|not_specified|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|GLIS3-related_disorder|not_provided": 1,
    "Monogenic_diabetes|not_specified|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|not_specified|GLIS3-related_disorder|Monogenic_diabetes|not_provided": 1,
    "not_provided|Monogenic_diabetes|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 2,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes|Inborn_genetic_diseases": 1,
    "GLIS3-related_disorder|Monogenic_diabetes|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Transitory_neonatal_diabetes_mellitus|not_specified|not_provided|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|GLIS3-related_disorder|not_provided": 1,
    "Neonatal_diabetes_mellitus_with_congenital_hypothyroidism|Monogenic_diabetes": 2,
    "GLIS3-related_disorder|Neonatal_diabetes_mellitus_with_congenital_hypothyroidism": 1,
    "Dicarboxylic_aminoaciduria": 84,
    "not_provided|Dicarboxylic_aminoaciduria": 10,
    "Dicarboxylic_aminoaciduria|not_provided": 14,
    "SLC1A1-related_disorder|not_provided|Dicarboxylic_aminoaciduria": 1,
    "Dicarboxylic_aminoaciduria|not_specified": 5,
    "SLC1A1-related_disorder": 2,
    "Dicarboxylic_aminoaciduria|SLC1A1-related_disorder|not_provided": 1,
    "not_specified|Dicarboxylic_aminoaciduria": 2,
    "Schizophrenia_18|Dicarboxylic_aminoaciduria": 2,
    "SLC1A1-related_disorder|Dicarboxylic_aminoaciduria": 1,
    "not_specified|Dicarboxylic_aminoaciduria|Schizophrenia_18": 1,
    "PLPP6-related_disorder": 9,
    "Psychotic_disorder": 1,
    "Budd-Chiari_syndrome": 6,
    "not_provided|Thrombocythemia_3": 2,
    "JAK2-related_disorder": 19,
    "not_provided|Acquired_polycythemia_vera|Primary_myelofibrosis|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Budd-Chiari_syndrome|Thrombocythemia_3|Acute_myeloid_leukemia": 1,
    "Budd-Chiari_syndrome|Acute_myeloid_leukemia|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Acquired_polycythemia_vera|Primary_myelofibrosis|Thrombocythemia_3|not_specified|not_provided": 1,
    "not_provided|Premature_ovarian_failure": 1,
    "JAK2-related_disorder|not_provided": 14,
    "not_provided|JAK2-related_disorder": 5,
    "JAK2-related_disorder|Inborn_genetic_diseases": 1,
    "JAK2-related_disorder|not_specified|not_provided": 2,
    "Thrombocythemia_3": 9,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation": 46,
    "ERYTHROCYTOSIS|_JAK2-RELATED|_SOMATIC": 1,
    "Acquired_polycythemia_vera": 4,
    "Acquired_polycythemia_vera|Primary_myelofibrosis|Acute_myeloid_leukemia|Budd-Chiari_syndrome|Thrombocythemia_3|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|not_provided|JAK2-related_disorder": 1,
    "Hereditary_cancer|not_specified|not_provided|Acquired_polycythemia_vera|Thrombocythemia_3|Budd-Chiari_syndrome|Primary_myelofibrosis": 1,
    "Primary_myelofibrosis|Splenomegaly|JAK2-related_disorder|Polycythemia|Budd-Chiari_syndrome|Acute_myeloid_leukemia|Acquired_polycythemia_vera|Thrombocythemia_3|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|not_provided|Myeloproliferative_disorder|Budd-Chiari_syndrome|_susceptibility_to|_somatic": 1,
    "JAK2-related_disorder|Budd-Chiari_syndrome|Acute_myeloid_leukemia|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Acquired_polycythemia_vera|Primary_myelofibrosis|Thrombocythemia_3|not_specified|not_provided": 1,
    "Thrombocythemia_3|not_provided": 1,
    "not_specified|not_provided|Inherited_susceptibility_to_asthma": 1,
    "Acute_myeloid_leukemia|Acquired_polycythemia_vera|Thrombocythemia_3|not_provided": 1,
    "Inborn_genetic_diseases|Thrombocythemia_3": 1,
    "Budd-Chiari_syndrome|Primary_myelofibrosis|Acute_myeloid_leukemia|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Acquired_polycythemia_vera|Thrombocythemia_3|not_provided": 1,
    "Acquired_polycythemia_vera|Thrombocythemia_3|Budd-Chiari_syndrome|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Primary_myelofibrosis|Acute_myeloid_leukemia|JAK2-related_disorder": 1,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Acquired_polycythemia_vera|Budd-Chiari_syndrome|Acute_myeloid_leukemia|Thrombocythemia_3|Primary_myelofibrosis": 1,
    "SMALL_ROUND_CELL_TUMOR": 1,
    "JAK2-related_disorder|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Primary_myelofibrosis|Acquired_polycythemia_vera|Budd-Chiari_syndrome|Acute_myeloid_leukemia|Thrombocythemia_3|not_specified|not_provided": 1,
    "not_specified|not_provided|Thrombocythemia_3": 1,
    "Budd-Chiari_syndrome|not_provided": 1,
    "RIC1-related_disorder": 6,
    "Catifa_syndrome": 8,
    "Catifa_syndrome|not_provided": 4,
    "not_provided|RIC1-related_disorder": 1,
    "Catifa_syndrome|not_specified": 1,
    "Glycine_encephalopathy|not_specified|not_provided": 4,
    "GLDC-related_disorder|not_provided|Inborn_genetic_diseases|Glycine_encephalopathy": 1,
    "not_specified|Glycine_encephalopathy|not_provided": 6,
    "GLDC-related_disorder|Glycine_encephalopathy|not_provided": 3,
    "Abnormal_brain_morphology|not_specified|Glycine_encephalopathy": 1,
    "Inborn_genetic_diseases|not_specified|Glycine_encephalopathy|Glycine_encephalopathy_1|not_provided": 1,
    "Glycine_encephalopathy_1|Glycine_encephalopathy|not_provided": 5,
    "GLDC-related_disorder|Glycine_encephalopathy|Intellectual_disability|Glycine_encephalopathy_1|not_provided": 1,
    "Glycine_encephalopathy|not_provided|GLDC-related_disorder": 2,
    "not_specified|Glycine_encephalopathy|Glycine_encephalopathy_1|not_provided": 1,
    "GLDC-related_disorder|Glycine_encephalopathy|Glycine_encephalopathy_1": 2,
    "not_provided|Inborn_genetic_diseases|Glycine_encephalopathy": 5,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|not_specified": 1,
    "Glycine_encephalopathy_1|not_specified|Glycine_encephalopathy": 2,
    "GLDC-related_disorder|not_provided|Glycine_encephalopathy": 6,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|Inborn_genetic_diseases|not_provided": 1,
    "Glycine_encephalopathy|not_specified|Glycine_encephalopathy_1": 2,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|not_provided": 3,
    "Glycine_encephalopathy|GLDC-related_disorder|not_provided": 1,
    "Glycine_encephalopathy|not_provided|not_specified": 3,
    "not_provided|GLDC-related_disorder|Glycine_encephalopathy_1|Glycine_encephalopathy": 1,
    "GLDC-related_disorder|Glycine_encephalopathy": 4,
    "Inborn_genetic_diseases|Glycine_encephalopathy|not_specified|not_provided": 1,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|Inborn_genetic_diseases": 1,
    "GLDC-related_disorder": 4,
    "Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy|Inborn_genetic_diseases": 1,
    "not_provided|Glycine_encephalopathy|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Glycine_encephalopathy|not_specified": 1,
    "Glycine_encephalopathy|GLDC-related_disorder": 6,
    "Glycine_encephalopathy_1|not_specified|not_provided|Glycine_encephalopathy": 2,
    "Glycine_encephalopathy|not_provided|Inborn_genetic_diseases": 2,
    "Smith-Magenis_Syndrome-like|Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Glycine_encephalopathy|GLDC-related_disorder": 1,
    "Glycine_encephalopathy_1|Retinitis_pigmentosa|Glycine_encephalopathy": 1,
    "not_provided|GLDC-related_disorder|Intellectual_disability|Glycine_encephalopathy": 1,
    "not_provided|GLDC-related_disorder|Glycine_encephalopathy": 2,
    "Inborn_genetic_diseases|Glycine_encephalopathy_1|Glycine_encephalopathy|not_provided": 1,
    "GLDC-related_disorder|Generalized_epilepsy|Global_developmental_delay|Obesity|Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy": 1,
    "not_specified|Glycine_encephalopathy_1|not_provided|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy_1|GLDC-related_disorder|Glycine_encephalopathy": 1,
    "not_provided|Glycine_encephalopathy|Glycine_encephalopathy_1": 2,
    "Glycine_encephalopathy_1|Inborn_genetic_diseases|not_provided|Glycine_encephalopathy": 1,
    "Inborn_genetic_diseases|Glycine_encephalopathy|Glycine_encephalopathy_1|not_provided": 1,
    "GLDC-related_disorder|Glycine_encephalopathy|Glycine_encephalopathy_1|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|See_cases|Glycine_encephalopathy|not_provided|Glycine_encephalopathy_1": 1,
    "Glycine_encephalopathy|GLDC-related_disorder|not_specified": 1,
    "Glycine_encephalopathy|not_provided|Glycine_encephalopathy_1": 1,
    "GLDC-related_disorder|not_specified|Glycine_encephalopathy|not_provided": 2,
    "Glycine_encephalopathy|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Glycine_encephalopathy_1|Glycine_encephalopathy": 1,
    "GLDC-related_disorder|Glycine_encephalopathy|not_provided|Glycine_encephalopathy_1|Inborn_genetic_diseases": 1,
    "Glycine_encephalopathy_1|GLDC-related_disorder|Inborn_genetic_diseases|not_provided|Glycine_encephalopathy": 1,
    "Inborn_genetic_diseases|Glycine_encephalopathy|not_provided|not_specified": 1,
    "Glycine_encephalopathy|Glycine_encephalopathy_1|not_provided|GLDC-related_disorder": 1,
    "not_provided|GLDC-related_disorder|not_specified|Glycine_encephalopathy": 1,
    "not_provided|Glycine_encephalopathy|GLDC-related_disorder|Inborn_genetic_diseases": 1,
    "GLDC-related_disorder|Glycine_encephalopathy_1|Glycine_encephalopathy": 1,
    "KDM4C-related_disorder": 2,
    "Enchondromatosis": 5,
    "KDM4C-related_disorder|Maffucci_syndrome": 1,
    "not_provided|PTPRD-related_disorder": 15,
    "PTPRD-related_disorder|not_provided": 8,
    "PTPRD-related_disorder": 29,
    "not_specified|PTPRD-related_disorder": 2,
    "Oculocutaneous_albinism_type_3": 34,
    "Oculocutaneous_albinism_type_3|not_provided": 12,
    "Oculocutaneous_albinism_type_3|MELANESIAN_BLOND_HAIR": 7,
    "Oculocutaneous_albinism_type_3|TYRP1-related_disorder": 1,
    "not_specified|Oculocutaneous_albinism_type_3|TYRP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Oculocutaneous_albinism_type_3": 1,
    "not_specified|Oculocutaneous_albinism_type_3|not_provided": 6,
    "not_provided|Oculocutaneous_albinism_type_3": 17,
    "TYRP1-related_disorder|Oculocutaneous_albinism_type_3|MELANESIAN_BLOND_HAIR|not_provided": 2,
    "not_specified|Oculocutaneous_albinism_type_3|not_provided|MELANESIAN_BLOND_HAIR": 1,
    "Nonsyndromic_Oculocutaneous_Albinism": 11,
    "MELANESIAN_BLOND_HAIR|not_provided": 1,
    "not_specified|not_provided|Oculocutaneous_albinism_type_3": 1,
    "not_provided|Oculocutaneous_albinism_type_3|MELANESIAN_BLOND_HAIR": 5,
    "TYRP1-related_disorder|not_provided": 3,
    "not_specified|not_provided|Oculocutaneous_albinism_type_3|TYRP1-related_disorder": 1,
    "not_provided|ALBINISM|_OCULOCUTANEOUS|_TYPE_II|_MODIFIER_OF|Oculocutaneous_albinism_type_3|MELANESIAN_BLOND_HAIR|TYRP1-related_disorder": 1,
    "Oculocutaneous_albinism_type_3|MELANESIAN_BLOND_HAIR|not_provided": 3,
    "TYRP1-related_disorder": 2,
    "not_provided|TYRP1-related_disorder": 3,
    "Ocular_albinism": 3,
    "not_specified|not_provided|TYRP1-related_disorder": 1,
    "Oculocutaneous_albinism_type_3|not_specified|not_provided": 3,
    "not_provided|TYRP1-related_disorder|Oculocutaneous_albinism_type_3": 2,
    "not_provided|Oculocutaneous_albinism_type_3|not_specified": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|not_provided|Oculocutaneous_albinism_type_3|MELANESIAN_BLOND_HAIR|TYRP1-related_disorder": 1,
    "MELANESIAN_BLOND_HAIR|Oculocutaneous_albinism_type_3|not_provided|Albinism": 1,
    "not_provided|Ocular_albinism|Oculocutaneous_albinism_type_3": 1,
    "not_specified|Oculocutaneous_albinism_type_3": 1,
    "Oculocutaneous_albinism_type_3|Albinism|not_provided|MELANESIAN_BLOND_HAIR": 1,
    "Oculocutaneous_albinism_type_3|not_provided|not_specified": 2,
    "not_provided|not_specified|Oculocutaneous_albinism_type_3": 1,
    "not_provided|not_specified|MELANESIAN_BLOND_HAIR|Oculocutaneous_albinism_type_3": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Nonsyndromic_Oculocutaneous_Albinism|Oculocutaneous_albinism_type_3": 1,
    "MELANESIAN_BLOND_HAIR|Oculocutaneous_albinism_type_3|not_provided|not_specified": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|MPDZ-related_disorder": 1,
    "MPDZ-related_disorder": 11,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided|MPDZ-related_disorder": 2,
    "MPDZ-related_disorder|not_provided": 26,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2": 35,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|MPDZ-related_disorder|not_provided": 1,
    "not_provided|MPDZ-related_disorder": 18,
    "Inborn_genetic_diseases|MPDZ-related_disorder": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|Inborn_genetic_diseases": 2,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided|Inborn_genetic_diseases": 2,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided": 17,
    "not_provided|Inborn_genetic_diseases|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2": 2,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|MPDZ-related_disorder": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_specified|not_provided": 3,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2": 13,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2": 1,
    "MPDZ-related_disorder|not_specified|not_provided": 3,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided|Congenital_hydrocephalus": 1,
    "Inborn_genetic_diseases|not_provided|MPDZ-related_disorder|not_specified": 1,
    "MPDZ-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|MPDZ-related_disorder": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided|MPDZ-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|MPDZ-related_disorder|not_provided": 2,
    "MPDZ-related_disorder|not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2": 1,
    "MPDZ-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided": 1,
    "MPDZ-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Nonsyndromic_hearing_impairment|not_provided": 1,
    "Inborn_genetic_diseases|Meniere_disease|MPDZ-related_disorder|not_provided": 1,
    "MPDZ-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|MPDZ-related_disorder|not_specified": 1,
    "not_provided|not_specified|MPDZ-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|Autosomal_dominant_retinitis_pigmentosa|Meniere_disease": 1,
    "MPDZ-related_disorder|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|not_provided": 1,
    "not_specified|not_provided|MPDZ-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2|MPDZ-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Hydrocephalus|_nonsyndromic|_autosomal_recessive_2": 1,
    "Macrocephaly|_acquired|_with_impaired_intellectual_development": 33,
    "NFIB-related_disorder|not_provided": 2,
    "NFIB-related_disorder": 9,
    "Inborn_genetic_diseases|NFIB-related_disorder": 1,
    "not_provided|NFIB-related_disorder": 1,
    "Macrocephaly|_acquired|_with_impaired_intellectual_development|Inborn_genetic_diseases": 1,
    "Macrocephaly|Intellectual_disability|Macrocephaly|_acquired|_with_impaired_intellectual_development": 4,
    "Macrocephaly|Intellectual_disability": 1,
    "NFIB-related_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Macrocephaly|_acquired|_with_impaired_intellectual_development": 1,
    "Macrocephaly|_acquired|_with_impaired_intellectual_development|Macrocephaly|Intellectual_disability|Marfanoid_habitus_and_intellectual_disability|not_provided": 1,
    "Macrocephaly|_acquired|_with_impaired_intellectual_development|not_provided": 3,
    "not_provided|Macrocephaly|_acquired|_with_impaired_intellectual_development|Macrocephaly|Intellectual_disability": 1,
    "Macrocephaly|_acquired|_with_impaired_intellectual_development|not_provided|Intellectual_disability|Macrocephaly": 1,
    "Oculotrichoanal_syndrome": 108,
    "Oculotrichoanal_syndrome|not_provided": 38,
    "not_provided|Oculotrichoanal_syndrome": 42,
    "BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2": 247,
    "not_provided|FREM1-related_disorder": 9,
    "not_provided|Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2": 7,
    "not_provided|Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome": 15,
    "not_specified|not_provided|Oculotrichoanal_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2": 3,
    "BNAR_syndrome": 6,
    "FREM1-related_disorder|not_provided": 14,
    "Oculotrichoanal_syndrome|not_provided|BNAR_syndrome|Trigonocephaly_2": 5,
    "Oculotrichoanal_syndrome|not_provided|BNAR_syndrome": 1,
    "FREM1-related_disorder": 25,
    "Inborn_genetic_diseases|BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome": 13,
    "not_provided|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2": 9,
    "Inborn_genetic_diseases|not_provided|Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome": 1,
    "BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|Inborn_genetic_diseases": 14,
    "not_provided|Inborn_genetic_diseases|Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2": 1,
    "not_provided|Oculotrichoanal_syndrome|FREM1-related_disorder": 7,
    "Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2|not_provided": 8,
    "FREM1-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Oculotrichoanal_syndrome": 3,
    "not_provided|Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome|Inborn_genetic_diseases": 1,
    "Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2": 14,
    "BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2": 2,
    "not_provided|FREM1-related_disorder|Oculotrichoanal_syndrome": 1,
    "not_provided|Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome": 5,
    "not_provided|FREM1-related_disorder|BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome": 1,
    "Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome": 3,
    "Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Oculotrichoanal_syndrome|not_specified|not_provided": 7,
    "BNAR_syndrome|Oculotrichoanal_syndrome|FREM1-related_disorder": 1,
    "Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|FREM1-related_disorder": 1,
    "not_provided|Oculotrichoanal_syndrome|BNAR_syndrome": 1,
    "not_provided|Oculotrichoanal_syndrome|Inborn_genetic_diseases|BNAR_syndrome|Trigonocephaly_2": 2,
    "BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|not_provided": 6,
    "Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Oculotrichoanal_syndrome": 1,
    "Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2": 8,
    "Oculotrichoanal_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "FREM1-related_disorder|not_provided|Oculotrichoanal_syndrome": 3,
    "Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|not_provided": 7,
    "Oculotrichoanal_syndrome|not_provided|FREM1-related_disorder": 3,
    "Oculotrichoanal_syndrome|not_provided|not_specified": 7,
    "Inborn_genetic_diseases|FREM1-related_disorder|not_provided": 1,
    "FREM1-related_disorder|Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Oculotrichoanal_syndrome": 1,
    "Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome|FREM1-related_disorder": 1,
    "Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|not_provided|FREM1-related_disorder": 1,
    "Oculotrichoanal_syndrome|not_provided|Inborn_genetic_diseases|BNAR_syndrome|Trigonocephaly_2": 3,
    "FREM1-related_disorder|Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|not_provided": 4,
    "not_provided|Oculotrichoanal_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2": 2,
    "Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Oculotrichoanal_syndrome|Inborn_genetic_diseases|BNAR_syndrome|Trigonocephaly_2": 6,
    "not_provided|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|Inborn_genetic_diseases": 1,
    "Oculotrichoanal_syndrome|BNAR_syndrome|not_provided|Trigonocephaly_2": 1,
    "not_provided|Oculotrichoanal_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|FREM1-related_disorder": 1,
    "Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2|Inborn_genetic_diseases|not_provided": 1,
    "BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|Inborn_genetic_diseases": 1,
    "BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|not_provided|FREM1-related_disorder": 1,
    "Trigonocephaly_2": 2,
    "not_provided|Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome": 3,
    "not_specified|Oculotrichoanal_syndrome|not_provided": 3,
    "FREM1-related_disorder|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2": 1,
    "Inborn_genetic_diseases|not_provided|BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome": 1,
    "Inborn_genetic_diseases|Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2|not_provided": 3,
    "BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|FREM1-related_disorder": 1,
    "Inborn_genetic_diseases|Trigonocephaly_2": 1,
    "Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2|not_provided|Inborn_genetic_diseases": 1,
    "Oculotrichoanal_syndrome|FREM1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome": 2,
    "FREM1-related_disorder|not_provided|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|Inborn_genetic_diseases": 1,
    "Oculotrichoanal_syndrome|Inborn_genetic_diseases": 1,
    "BNAR_syndrome|Oculotrichoanal_syndrome": 2,
    "Inborn_genetic_diseases|Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome|not_provided|FREM1-related_disorder": 1,
    "Oculotrichoanal_syndrome|not_provided|FREM1-related_disorder|BNAR_syndrome|Trigonocephaly_2": 1,
    "Oculotrichoanal_syndrome|FREM1-related_disorder|BNAR_syndrome|Trigonocephaly_2": 1,
    "Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Trigonocephaly_2|Oculotrichoanal_syndrome|BNAR_syndrome|Inborn_genetic_diseases": 1,
    "BNAR_syndrome|not_provided": 1,
    "not_provided|BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome": 2,
    "BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome|not_provided": 1,
    "FREM1-related_disorder|BNAR_syndrome|Trigonocephaly_2|Oculotrichoanal_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Chronic_kidney_disease|Congenital_anomaly_of_kidney_and_urinary_tract|Inborn_genetic_diseases|Oculotrichoanal_syndrome": 1,
    "Irido-corneo-trabecular_dysgenesis|Rieger_anomaly|Trigonocephaly_2|not_provided|Oculotrichoanal_syndrome|BNAR_syndrome": 1,
    "FREM1-related_disorder|Oculotrichoanal_syndrome|not_provided": 1,
    "FREM1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Oculotrichoanal_syndrome|FREM1-related_disorder": 1,
    "not_specified|not_provided|Oculotrichoanal_syndrome|Congenital_diaphragmatic_hernia": 1,
    "Oculotrichoanal_syndrome|Trigonocephaly_2|BNAR_syndrome": 1,
    "not_provided|FREM1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|FREM1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|FREM1-related_disorder": 1,
    "Inborn_genetic_diseases|BNAR_syndrome|Oculotrichoanal_syndrome|Trigonocephaly_2|not_provided": 1,
    "not_provided|Oculotrichoanal_syndrome|BNAR_syndrome|Trigonocephaly_2|Inborn_genetic_diseases": 1,
    "Trigonocephaly_2|BNAR_syndrome|Oculotrichoanal_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Oculotrichoanal_syndrome|BNAR_syndrome": 2,
    "not_provided|Lower_urinary_tract_obstruction|_congenital": 1,
    "not_provided|BNC2-related_disorder": 7,
    "not_provided|Hypotension": 7,
    "BNC2-related_disorder|Amelogenesis_imperfecta": 1,
    "BNC2-related_disorder|Hypotension|not_provided": 4,
    "BNC2-related_disorder|Hypotension|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|BNC2-related_disorder": 2,
    "Lower_urinary_tract_obstruction|_congenital|Lower_Urinary_Tract_Obstruction": 2,
    "BNC2-related_disorder|Lower_urinary_tract_obstruction|_congenital": 1,
    "Lower_urinary_tract_obstruction|_congenital": 4,
    "Hypotension|not_provided": 5,
    "Hypotension": 9,
    "BNC2-related_disorder|not_provided": 4,
    "Hypotension|not_specified|not_provided": 1,
    "BNC2-related_disorder": 4,
    "Lower_urinary_tract_obstruction|_congenital|BNC2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|BNC2-related_disorder": 1,
    "BNC2-related_disorder|not_provided|Hypotension": 1,
    "Inborn_genetic_diseases|BNC2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Lower_urinary_tract_obstruction|_congenital": 1,
    "ADAMTSL1-related_disorder": 7,
    "not_specified|ADAMTSL1-related_disorder": 2,
    "ADAMTSL1-related_disorder|not_specified": 1,
    "Abnormal_retinal_morphology|not_provided": 1,
    "Inborn_genetic_diseases|FOCAD-related_disorder|not_provided": 3,
    "FOCAD-related_disorder": 48,
    "FOCAD-related_disorder|not_provided": 40,
    "Liver_disease|_severe_congenital": 14,
    "not_provided|Inborn_genetic_diseases|FOCAD-related_disorder": 5,
    "not_provided|FOCAD-related_disorder": 35,
    "FOCAD-related_disorder|Liver_disease|_severe_congenital": 1,
    "FOCAD-related_disorder|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|FOCAD-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|FOCAD-related_disorder": 2,
    "FOCAD-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "FOCAD-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "FOCAD-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Multisystem_inflammatory_syndrome_in_children": 2,
    "KLHL9-related_disorder|not_provided|not_specified": 1,
    "KLHL9-related_disorder|not_provided": 2,
    "KLHL9-related_disorder": 1,
    "not_provided|KLHL9-related_disorder": 2,
    "KLHL9-related_distal_myopathy": 1,
    "IFNE-related_disorder": 1,
    "Diaphyseal_medullary_stenosis-bone_malignancy_syndrome": 103,
    "Diaphyseal_medullary_stenosis-bone_malignancy_syndrome|not_provided": 16,
    "MTAP-related_disorder|Diaphyseal_medullary_stenosis-bone_malignancy_syndrome|not_provided": 1,
    "Diaphyseal_medullary_stenosis-bone_malignancy_syndrome|MTAP-related_disorder": 1,
    "not_specified|Diaphyseal_medullary_stenosis-bone_malignancy_syndrome": 2,
    "MTAP-related_disorder|Diaphyseal_medullary_stenosis-bone_malignancy_syndrome": 1,
    "MTAP-related_disorder": 1,
    "not_provided|Diaphyseal_medullary_stenosis-bone_malignancy_syndrome": 3,
    "Melanoma-pancreatic_cancer_syndrome": 37,
    "Familial_melanoma|CDKN2A-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|CDKN2A-related_disorder": 1,
    "Familial_melanoma": 601,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 36,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 305,
    "Familial_melanoma|not_provided|Hereditary_cancer-predisposing_syndrome": 25,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified": 15,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified": 5,
    "Familial_melanoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 201,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 3,
    "not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 25,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "CDKN2A-related_disorder": 7,
    "not_specified|not_provided|Melanoma-pancreatic_cancer_syndrome": 2,
    "Melanoma-pancreatic_cancer_syndrome|not_specified|CDKN2A-related_disorder": 1,
    "Familial_melanoma|not_provided|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome": 2,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|CDKN2A-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma": 15,
    "Familial_pancreatic_carcinoma|Li-Fraumeni_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_provided": 19,
    "Familial_pancreatic_carcinoma|Li-Fraumeni_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 5,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma-pancreatic_cancer_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 8,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Melanoma_and_neural_system_tumor_syndrome|not_provided|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|not_specified|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Familial_melanoma": 5,
    "Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome": 7,
    "Familial_melanoma|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|CDKN2A-related_disorder|Melanoma-pancreatic_cancer_syndrome|not_provided|Familial_melanoma": 1,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|not_specified": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma-pancreatic_cancer_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|CDKN2A-related_disorder|not_provided|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "not_specified|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|not_provided": 1,
    "Familial_melanoma|not_specified|not_provided|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome": 1,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|CDKN2A-related_disorder|not_provided|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Malignant_tumor_of_urinary_bladder": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma_and_neural_system_tumor_syndrome": 2,
    "Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome": 4,
    "Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lip_and_oral_cavity_carcinoma|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma": 1,
    "not_provided|Familial_melanoma": 8,
    "Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|not_specified|not_provided|Hereditary_cancer|Familial_melanoma": 1,
    "not_specified|Melanoma_and_neural_system_tumor_syndrome|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Maffucci_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma-pancreatic_cancer_syndrome": 1,
    "Familial_melanoma|not_provided": 9,
    "Melanoma_and_neural_system_tumor_syndrome|not_provided|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma_and_neural_system_tumor_syndrome": 8,
    "CDKN2A-related_disorder|Melanoma|Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome": 1,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Familial_melanoma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Squamous_cell_lung_carcinoma|Familial_melanoma|not_provided": 1,
    "Melanoma-pancreatic_cancer_syndrome|Familial_melanoma": 2,
    "not_provided|CDKN2A-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|not_specified": 1,
    "Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "Familial_melanoma|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_melanoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma_and_neural_system_tumor_syndrome": 1,
    "Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Melanoma_and_neural_system_tumor_syndrome|not_specified|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 2,
    "not_provided|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma-pancreatic_cancer_syndrome": 4,
    "Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome": 3,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "CDKN2A-related_disorder|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Familial_pancreatic_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Familial_pancreatic_carcinoma|Familial_melanoma|not_provided": 1,
    "Familial_melanoma|Lip_and_oral_cavity_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Acute_lymphoid_leukemia|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome": 2,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma": 1,
    "Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome": 1,
    "Familial_melanoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|CDKN2A-related_disorder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|CDKN2A-related_disorder|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome": 1,
    "Melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|Squamous_cell_lung_carcinoma": 1,
    "Familial_melanoma|Melanoma-pancreatic_cancer_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_provided": 1,
    "Atypical_endometrial_hyperplasia|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_pancreatic_carcinoma|Li-Fraumeni_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome": 2,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Melanoma_and_neural_system_tumor_syndrome|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "CDKN2A-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_provided|not_specified|Li-Fraumeni_syndrome|Melanoma-pancreatic_cancer_syndrome": 1,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Familial_melanoma": 1,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CDKN2A-related_disorder|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|not_provided|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Melanoma_and_neural_system_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "Familial_pancreatic_carcinoma|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hepatocellular_carcinoma|Li-Fraumeni_syndrome|Melanoma-pancreatic_cancer_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "not_specified|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|CDKN2A-related_disorder": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|not_specified|not_provided": 1,
    "not_specified|CDKN2A-related_disorder|not_provided|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "CDKN2A-related_disorder|not_provided|Melanoma-pancreatic_cancer_syndrome": 1,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome": 2,
    "CDKN2A-related_disorder|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma-pancreatic_cancer_syndrome": 1,
    "Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome": 1,
    "not_specified|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 5,
    "Familial_melanoma|CDKN2A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Familial_melanoma|not_provided|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_provided": 1,
    "not_specified|CDKN2A-related_disorder|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome": 1,
    "CDKN2A-related_disorder|Osteoblastic_osteosarcoma|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Acute_lymphoid_leukemia|Familial_melanoma": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "CDKN2A-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Ovarian_cancer|not_specified|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|not_provided|Familial_melanoma": 1,
    "not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 2,
    "Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma": 3,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma": 1,
    "not_provided|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma_and_neural_system_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Familial_melanoma|not_specified": 11,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Squamous_cell_lung_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma_and_neural_system_tumor_syndrome|not_specified|Familial_melanoma": 1,
    "CDKN2A-related_disorder|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "CDKN2A-related_disorder|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Familial_melanoma": 1,
    "Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gastric_cancer|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|not_provided": 1,
    "Familial_pancreatic_carcinoma|Li-Fraumeni_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|not_specified|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CDKN2A-related_disorder|Familial_pancreatic_carcinoma|Li-Fraumeni_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma-pancreatic_cancer_syndrome": 1,
    "not_provided|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|not_provided": 1,
    "CDKN2A-related_disorder|Melanoma|Ovarian_neoplasm|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_melanoma|not_provided|Melanoma-pancreatic_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|CDKN2A-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|not_specified": 1,
    "not_provided|Melanoma-pancreatic_cancer_syndrome": 2,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "CDKN2A-related_disorder|not_provided|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CDKN2A-related_disorder|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|not_provided|CDKN2A-related_disorder": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma_and_neural_system_tumor_syndrome|not_provided": 1,
    "Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma": 3,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Melanoma-pancreatic_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Melanoma-pancreatic_cancer_syndrome|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome": 1,
    "Melanoma-pancreatic_cancer_syndrome|Melanoma_and_neural_system_tumor_syndrome|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_2|Melanoma_and_neural_system_tumor_syndrome|Melanoma-pancreatic_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma|Melanoma_and_neural_system_tumor_syndrome": 1,
    "CDKN2A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Three_Vessel_Coronary_Disease": 8,
    "Malignant_tumor_of_breast|Three_Vessel_Coronary_Disease": 1,
    "Three_Vessel_Coronary_Disease": 20,
    "Multiple_endocrine_neoplasia|not_specified|not_provided": 1,
    "not_specified|ELAVL2-related_disorder": 1,
    "Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies": 17,
    "Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies|not_provided": 7,
    "not_provided|Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies|PLAA-related_disorder": 1,
    "PLAA-related_disorder|not_provided": 5,
    "not_provided|PLAA-related_disorder": 2,
    "not_provided|Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies": 1,
    "Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies": 1,
    "IFT74-related_disorder": 61,
    "Inborn_genetic_diseases|IFT74-related_disorder": 3,
    "IFT74-related_disorder|not_provided": 56,
    "not_provided|IFT74-related_disorder": 26,
    "Joubert_syndrome_40": 4,
    "Bardet-Biedl_syndrome_22|not_provided": 2,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|IFT74-related_disorder": 1,
    "Joubert_syndrome_40|IFT74-related_disorder|Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|IFT74-related_disorder|not_provided|Bardet-Biedl_syndrome_22": 1,
    "Bardet-Biedl_syndrome_22|IFT74-related_disorder|not_provided": 2,
    "IFT74-related_disorder|not_provided|Inborn_genetic_diseases": 5,
    "IFT74-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "IFT74-related_disorder|not_provided|Bardet-Biedl_syndrome_22": 1,
    "Spermatogenic_failure_58|Multiple_Morphological_Anomalies_of_Sperm_Flagella_(MMAF)": 1,
    "IFT74-related_disorder|Joubert_syndrome_40|Bardet-Biedl_syndrome_22|not_provided": 1,
    "Bardet-Biedl_syndrome_22": 4,
    "Bardet-Biedl_syndrome|not_provided|Inborn_genetic_diseases|Joubert_syndrome_40|IFT74-related_disorder": 1,
    "not_provided|Joubert_syndrome_40": 2,
    "IFT74-related_disorder|not_provided|Inborn_genetic_diseases|Microcephaly": 1,
    "not_provided|IFT74-related_disorder|Optic_atrophy": 1,
    "IFT74-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|IFT74-related_disorder|not_provided": 2,
    "IFT74-related_disorder|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_40|Spermatogenic_failure_58|not_provided|IFT74-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|IFT74-related_disorder": 2,
    "not_provided|IFT74-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|IFT74-related_disorder": 3,
    "IFT74-related_disorder|Joubert_syndrome_40|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|IFT74-related_disorder|Joubert_syndrome_40|Spermatogenic_failure_58|Bardet-Biedl_syndrome_22": 1,
    "IFT74-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_22": 1,
    "Microcephaly|IFT74-related_disorder|not_provided": 1,
    "IFT74-related_disorder|not_specified|not_provided": 1,
    "not_provided|IFT74-related_disorder|Inborn_genetic_diseases|Joubert_syndrome": 1,
    "not_provided|Multiple_cutaneous_and_mucosal_venous_malformations": 6,
    "Multiple_cutaneous_and_mucosal_venous_malformations": 63,
    "Glaucoma_3|_primary_congenital|_E": 17,
    "Multiple_cutaneous_and_mucosal_venous_malformations|not_provided": 31,
    "TEK-related_disorder": 10,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Multiple_cutaneous_and_mucosal_venous_malformations": 2,
    "Inborn_genetic_diseases|Multiple_cutaneous_and_mucosal_venous_malformations|Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_E|TEK-related_disorder|not_provided": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_E": 3,
    "Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_E|Multiple_cutaneous_and_mucosal_venous_malformations": 2,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Glaucoma_3|_primary_congenital|_E|not_provided": 2,
    "Glaucoma_3|_primary_congenital|_E|Multiple_cutaneous_and_mucosal_venous_malformations|not_provided|not_specified": 1,
    "TEK-related_disorder|Multiple_cutaneous_and_mucosal_venous_malformations|not_provided": 1,
    "not_provided|Multiple_cutaneous_and_mucosal_venous_malformations|Inborn_genetic_diseases": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|not_provided|Inborn_genetic_diseases": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|TEK-related_disorder|not_specified|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_E|Multiple_cutaneous_and_mucosal_venous_malformations|not_specified|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_E|Multiple_cutaneous_and_mucosal_venous_malformations|not_provided": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|not_provided|Glaucoma_3|_primary_congenital|_E|not_specified": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Inborn_genetic_diseases|not_provided": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Glaucoma_3|_primary_congenital|_E": 2,
    "Multiple_cutaneous_and_mucosal_venous_malformations|not_provided|Segmental_undergrowth_associated_with_venous_malformation_without_capillary_component|Abnormal_cardiovascular_system_morphology|TEK-related_disorder": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|TEK-related_disorder": 1,
    "not_provided|TEK-related_disorder": 1,
    "not_provided|Vascular_malformation": 2,
    "Blue_rubber_bleb_nevus|Multiple_cutaneous_and_mucosal_venous_malformations": 1,
    "Ventricular_septal_defect|Blue_rubber_bleb_nevus|Abnormal_cardiovascular_system_morphology|Multiple_cutaneous_and_mucosal_venous_malformations|not_provided": 1,
    "Venous_malformation": 6,
    "Abnormal_cardiovascular_system_morphology|Vascular_malformation|Bockenheimer_syndrome|not_provided": 1,
    "Vascular_malformation|Abnormal_cardiovascular_system_morphology|not_provided": 1,
    "not_provided|Abnormal_cardiovascular_system_morphology|Multiple_cutaneous_and_mucosal_venous_malformations": 1,
    "not_provided|Vascular_malformation|Neutropenia|_severe_congenital|_2|_autosomal_dominant|Abnormal_cardiovascular_system_morphology|Segmental_undergrowth_associated_with_venous_malformation_without_capillary_component": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|not_specified|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_E|Multiple_cutaneous_and_mucosal_venous_malformations": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|not_provided|Glaucoma_3|_primary_congenital|_E": 1,
    "not_specified|Multiple_cutaneous_and_mucosal_venous_malformations|not_provided": 1,
    "Glaucoma_3|_primary_infantile|_B|Multiple_cutaneous_and_mucosal_venous_malformations": 1,
    "Segmental_undergrowth_associated_with_venous_malformation_without_capillary_component": 2,
    "Glaucoma_3|_primary_infantile|_B|Multiple_cutaneous_and_mucosal_venous_malformations|Glaucoma_3|_primary_congenital|_E": 1,
    "Abnormal_cardiovascular_system_morphology|Multiple_cutaneous_and_mucosal_venous_malformations": 1,
    "Vascular_malformation|not_provided": 2,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Vascular_malformation": 1,
    "Multiple_cutaneous_and_mucosal_venous_malformations|Abnormal_cardiovascular_system_morphology": 2,
    "Segmental_undergrowth_associated_with_venous_malformation_without_capillary_component|not_provided|Vascular_malformation": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 59,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 9,
    "Amyotrophic_Lateral_Sclerosis/Frontotemporal_Dementia": 17,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1|not_provided": 1,
    "C9orf72-related_disorder": 3,
    "Amyotrophic_Lateral_Sclerosis/Frontotemporal_Dementia|not_provided": 1,
    "not_provided|not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_1": 2,
    "Singleton-Merten_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|RIGI-related_disorder": 1,
    "not_provided|Singleton-Merten_syndrome_2": 5,
    "not_provided|RIGI-related_disorder": 3,
    "Singleton-Merten_syndrome_2|not_specified|not_provided": 1,
    "Singleton-Merten_syndrome_2|not_provided": 5,
    "not_provided|not_specified|Singleton-Merten_syndrome_2": 1,
    "RIGI-related_disorder|not_provided": 3,
    "Singleton-Merten_syndrome_2": 5,
    "RIGI-related_disorder": 3,
    "not_specified|not_provided|Singleton-Merten_syndrome_2": 1,
    "not_provided|Singleton-Merten_syndrome_2|not_specified": 1,
    "Retinitis_pigmentosa_31|not_provided": 5,
    "Retinal_dystrophy|not_specified|Retinitis_pigmentosa|not_provided": 2,
    "Retinitis_pigmentosa|not_provided|TOPORS-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_31": 1,
    "TOPORS-related_disorder|not_provided": 5,
    "Optic_atrophy|Retinitis_pigmentosa_31": 1,
    "not_provided|TOPORS-related_disorder": 3,
    "Retinitis_pigmentosa_31": 6,
    "Abnormality_of_retinal_pigmentation|Macular_dystrophy|Adult-onset_night_blindness|Pigmentary_retinopathy|Decreased_light-_and_dark-adapted_electroretinogram_amplitude|Abnormality_of_vision|Hypermetropia|not_provided|Retinitis_pigmentosa_31": 1,
    "Retinitis_pigmentosa_31|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_31": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_31": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_31": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_31": 1,
    "TOPORS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_31|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_31|TOPORS-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|TOPORS-related_disorder": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_specified|not_provided|Retinitis_pigmentosa_31": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|TOPORS-related_disorder": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_31": 1,
    "not_provided|Retinitis_pigmentosa_31": 2,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_31": 1,
    "not_provided|not_specified|TOPORS-related_disorder|Retinitis_pigmentosa": 1,
    "Abnormality_of_retinal_pigmentation|Macular_degeneration|Pigmentary_retinopathy|Blurred_vision|Retinitis_pigmentosa_31": 1,
    "TOPORS-related_disorder": 1,
    "TOPORS-related_disorder|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "Choroideremia": 67,
    "Retinal_dystrophy|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "TOPORS-related_retinopathy": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_31": 1,
    "not_provided|Retinal_dystrophy|TOPORS-related_disorder": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 2,
    "Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 2,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_provided": 6,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 34,
    "not_provided|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 2,
    "Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 3,
    "not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type": 1,
    "APTX-related_disorder|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|not_specified|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "APTX-related_disorder|Inborn_genetic_diseases|Hereditary_ataxia|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 7,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type": 1,
    "not_specified|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_provided": 3,
    "not_provided|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|not_specified|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Inborn_genetic_diseases": 1,
    "APTX-related_disorder|not_specified|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_provided|APTX-related_disorder|not_specified|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_specified|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 2,
    "not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Inborn_genetic_diseases": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_specified": 1,
    "APTX-related_disorder|not_provided": 1,
    "not_provided|not_specified|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_specified|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_provided|APTX-related_disorder": 1,
    "Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_provided|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type|not_specified": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_specified|not_provided": 1,
    "not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_specified": 2,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Coenzyme_Q10_deficiency|_Oculomotor_Apraxia_Type": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "not_specified|APTX-related_disorder|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "Combined_low_LDL_and_fibrinogen": 1,
    "not_specified|not_provided|B4GALT1-congenital_disorder_of_glycosylation": 1,
    "B4GALT1-congenital_disorder_of_glycosylation": 3,
    "B4GALT1-related_disorder": 3,
    "B4GALT1-congenital_disorder_of_glycosylation|not_provided": 3,
    "B4GALT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|B4GALT1-congenital_disorder_of_glycosylation|not_provided": 1,
    "B4GALT1-related_disorder|not_provided": 1,
    "B4GALT1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_provided|B4GALT1-related_disorder": 3,
    "B4GALT1-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "not_specified|B4GALT1-related_disorder": 1,
    "not_provided|B4GALT1-congenital_disorder_of_glycosylation": 1,
    "GLYCEROL_QUANTITATIVE_TRAIT_LOCUS": 1,
    "not_specified|AQP7-related_condition": 1,
    "OBESITY_(BMIQ17)|_SUSCEPTIBILITY_TO": 1,
    "AQP3-related_disorder": 3,
    "GIL_BLOOD_GROUP": 1,
    "Thyroiditis": 1,
    "Spastic_paraplegia_80|_autosomal_dominant": 24,
    "Inborn_genetic_diseases|Spastic_paraplegia_80|_autosomal_dominant|UBAP1-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia_80|_autosomal_dominant|not_provided": 1,
    "UBAP1-related_disorder|not_provided": 3,
    "UBAP1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Spastic_paraplegia_80|_autosomal_dominant": 1,
    "not_provided|Spastic_paraplegia_80|_autosomal_dominant": 1,
    "Intellectual_developmental_disorder_with_or_without_peripheral_neuropathy": 3,
    "NUDT2-associated_condition|Complex_neurodevelopmental_disorder|not_provided|Intellectual_developmental_disorder_with_or_without_peripheral_neuropathy|Intellectual_disability": 1,
    "Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive|not_provided": 4,
    "Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive": 31,
    "Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "Dysarthria": 1,
    "MYORG-related_disorder": 6,
    "not_provided|MYORG-related_disorder": 7,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive": 3,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive|MYORG-related_disorder": 1,
    "not_specified|Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive|not_provided": 1,
    "MYORG-related_disorder|not_provided": 5,
    "not_specified|MYORG-related_disorder": 1,
    "not_specified|Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive": 1,
    "not_specified|Basal_ganglia_calcification|_idiopathic|_7|_autosomal_recessive|MYORG-related_disorder|not_provided": 1,
    "Kartagener_syndrome|Primary_ciliary_dyskinesia": 36,
    "not_provided|Primary_ciliary_dyskinesia|DNAI1-related_disorder|not_specified": 1,
    "DNAI1-related_disorder|Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "DNAI1-related_disorder": 2,
    "DNAI1-related_disorder|Primary_ciliary_dyskinesia|Kartagener_syndrome|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia|Kartagener_syndrome|DNAI1-related_disorder": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "DNAI1-related_disorder|Primary_ciliary_dyskinesia|not_provided|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia|DNAI1-related_disorder": 6,
    "Primary_ciliary_dyskinesia|DNAI1-related_disorder|Kartagener_syndrome": 1,
    "Kartagener_syndrome|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Kartagener_syndrome": 3,
    "Kartagener_syndrome|DNAI1-related_disorder|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome": 6,
    "DNAI1-related_disorder|Kartagener_syndrome|Primary_ciliary_dyskinesia": 2,
    "not_provided|Kartagener_syndrome|Primary_ciliary_dyskinesia": 3,
    "not_specified|not_provided|Kartagener_syndrome|Primary_ciliary_dyskinesia": 2,
    "not_specified|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "not_provided|Kartagener_syndrome": 2,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "Kartagener_syndrome|Primary_ciliary_dyskinesia|not_specified": 1,
    "not_provided|not_specified|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia|Kartagener_syndrome|not_provided": 3,
    "DNAI1-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Kartagener_syndrome|not_specified": 1,
    "not_provided|See_cases|Kartagener_syndrome|Primary_ciliary_dyskinesia": 1,
    "DNAI1-related_disorder|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "DNAI1-related_disorder|not_specified|Primary_ciliary_dyskinesia": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Kartagener_syndrome|Primary_ciliary_dyskinesia|See_cases": 1,
    "Kartagener_syndrome|not_specified": 1,
    "Primary_ciliary_dyskinesia|not_provided|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia|Infertility_disorder|Kartagener_syndrome|Male_infertility": 1,
    "Kartagener_syndrome|Primary_ciliary_dyskinesia|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16": 69,
    "Amyotrophic_lateral_sclerosis_type_16": 6,
    "not_provided|Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 1,
    "Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 66,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2|Inborn_genetic_diseases": 7,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16|not_provided|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16|Inborn_genetic_diseases": 7,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 1,
    "Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2|not_specified": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16": 2,
    "not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16|SIGMAR1-related_disorder": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2": 4,
    "Amyotrophic_lateral_sclerosis_type_16|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2|not_specified": 2,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_16|Autosomal_recessive_distal_spinal_muscular_atrophy_2": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_2|Amyotrophic_lateral_sclerosis_type_16|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_2|not_specified|Amyotrophic_lateral_sclerosis_type_16|not_provided": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 488,
    "Inborn_genetic_diseases|Galactosemia|not_specified|not_provided|Classical_galactosemia|_homozygous_Duarte-type|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 11,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|GALT-related_disorder": 1,
    "Galactosemia": 63,
    "Inborn_genetic_diseases|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|Galactosemia": 1,
    "not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|GALT-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|Galactosemia": 10,
    "not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 35,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_provided": 28,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_specified": 9,
    "GALT-related_disorder": 4,
    "Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 31,
    "not_specified|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 2,
    "not_provided|not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 3,
    "Galactosemia|not_provided": 6,
    "Inborn_genetic_diseases|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 4,
    "GALT_POLYMORPHISM": 1,
    "GALT-related_disorder|not_specified|Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 15,
    "Galactosemia|not_specified|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 6,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 2,
    "GALT-related_disorder|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Galactosemia|not_specified|not_provided": 2,
    "GALT-related_disorder|not_provided|Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "GALT-related_disorder|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 3,
    "Galactosemia|not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 6,
    "not_provided|Galactosemia|not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_provided|Galactosemia": 2,
    "not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_provided": 3,
    "GALT-related_disorder|Inborn_genetic_diseases|Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|See_cases": 1,
    "not_specified|Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 4,
    "GALT-related_disorder|Galactosemia|not_specified|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "GALT-related_disorder|Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 4,
    "not_provided|Galactosemia": 2,
    "Inborn_genetic_diseases|not_provided|Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 2,
    "not_specified|Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 3,
    "not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_provided|Galactosemia": 1,
    "not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|Galactosemia": 5,
    "GALT-related_disorder|Inborn_genetic_diseases|Galactosemia|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_provided|not_specified": 1,
    "not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_specified": 3,
    "GALT-related_disorder|not_provided": 1,
    "GALT-related_disorder|not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "not_specified|Galactosemia": 1,
    "Premature_ovarian_failure|not_provided|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|GALT-related_disorder|Galactosemia": 1,
    "Galactosemia|not_provided|not_specified|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 2,
    "Galactosemia|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|GALT-related_disorder|Galactosemia": 1,
    "Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_provided": 2,
    "not_specified|not_provided|Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|Galactosemia|not_specified": 1,
    "Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|Inborn_genetic_diseases|not_provided": 1,
    "GALT-related_disorder|Galactosemia|not_provided|GALT_POLYMORPHISM_(DUARTE|_D2)|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase": 1,
    "Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|GALT-related_disorder|not_specified": 1,
    "Galactosemia|Deficiency_of_UDPglucose-hexose-1-phosphate_uridylyltransferase|not_specified": 1,
    "IL11RA-related_disorder": 4,
    "not_provided|IL11RA-related_disorder": 5,
    "Craniosynostosis_and_dental_anomalies": 9,
    "Craniosynostosis_syndrome|not_provided": 2,
    "Craniosynostosis_and_dental_anomalies|not_provided": 1,
    "not_provided|Craniosynostosis_and_dental_anomalies": 2,
    "not_provided|Skeletal_myopathy|Peripheral_neuropathy": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_provided": 2,
    "Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 3,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 15,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 8,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Intellectual_disability": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 227,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases": 7,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases|not_specified|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 147,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 10,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_provided": 12,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided": 8,
    "not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Inborn_genetic_diseases": 3,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Inborn_genetic_diseases|not_specified": 1,
    "VCP-related_disorder|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_specified": 1,
    "VCP-related_disorder": 8,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 10,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|VCP-related_disorder": 2,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 2,
    "VCP-related_disorder|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 2,
    "VCP-related_disorder|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|VCP-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases|not_provided": 3,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 3,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|VCP-related_disorder|Inborn_genetic_diseases|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_specified": 1,
    "VCP-related_disorder|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 4,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|VCP-related_disorder": 5,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_specified|Charcot-Marie-Tooth_disease_type_2Y|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Childhood_Onset_VCP-related_Neurodevelopmental_Disorder": 5,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases|VCP-related_disorder|not_specified|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_specified|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2Y": 1,
    "VCP-related_multisystem_proteinopathy": 1,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|VCP-related_disorder|Inborn_genetic_diseases": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_specified": 2,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases|VCP-related_disorder|not_provided": 1,
    "FRONTOTEMPORAL_DEMENTIA_WITHOUT_AMYOTROPHIC_LATERAL_SCLEROSIS_6|_WITH_NEUROFIBRILLARY_TANGLES|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Charcot-Marie-Tooth_disease_type_2Y|not_provided": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_specified|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|VCP-related_disorder|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|VCP-related_disorder|not_provided|not_specified|Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_specified|not_provided": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2Y": 2,
    "Inborn_genetic_diseases|not_specified|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 2,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 3,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Charcot-Marie-Tooth_disease_type_2Y|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Charcot-Marie-Tooth_disease_type_2Y|Childhood_Onset_VCP-related_Neurodevelopmental_Disorder": 1,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|VCP-related_disorder": 1,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Lewy_body_dementia": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Charcot-Marie-Tooth_disease_type_2Y|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_provided": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2Y|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|VCP-related_disorder|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Amyotrophic_lateral_sclerosis_type_6": 118,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inborn_genetic_diseases|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_specified": 1,
    "not_provided|VCP-related_disorder": 2,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|not_provided|Inborn_genetic_diseases": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided|Inborn_genetic_diseases": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 1,
    "VCP-related_disorder|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|VCP-related_disorder": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "VCP-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Charcot-Marie-Tooth_disease_type_2Y": 1,
    "Progressive_muscle_weakness": 1,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|VCP-related_disorder|Spastic_paraplegia|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|INCLUSION_BODY_MYOPATHY_WITHOUT_EARLY-ONSET_PAGET_DISEASE_AND_FRONTOTEMPORAL_DEMENTIA_1": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided|not_specified": 2,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6": 1,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Charcot-Marie-Tooth_disease_type_2Y|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1": 1,
    "VCP-related_disorder|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Intellectual_disability|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|not_specified|not_provided|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "not_provided|Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_6|Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia_type_1|Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant|not_provided": 1,
    "Fanconi_anemia_complementation_group_G": 126,
    "Fanconi_anemia_complementation_group_G|not_provided": 4,
    "FANCG-related_disorder": 3,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_G|not_specified|not_provided": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_G": 7,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases": 10,
    "Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases": 9,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_G": 58,
    "FANCG-related_disorder|Fanconi_anemia_complementation_group_G|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia": 56,
    "Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases|Fanconi_anemia": 9,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 6,
    "Fanconi_anemia|Ovarian_cancer|Fanconi_anemia_complementation_group_G": 1,
    "FANCG-related_disorder|Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_G|Fanconi_anemia": 7,
    "FANCG-related_disorder|not_provided|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia|not_provided": 2,
    "Fanconi_anemia_complementation_group_G|not_specified": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Inclusion_Body_Myopathy|_Dominant|Fanconi_anemia_complementation_group_G|Amyotrophic_Lateral_Sclerosis|_Dominant|not_specified|not_provided": 1,
    "Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant|Fanconi_anemia_complementation_group_G|Fanconi_anemia|not_specified|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 5,
    "Fanconi_anemia|FANCG-related_disorder|Fanconi_anemia_complementation_group_G": 2,
    "Inborn_genetic_diseases|FANCG-related_disorder": 1,
    "Fanconi_anemia|not_specified|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 1,
    "Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant|FANCG-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_G": 7,
    "Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases|not_specified|Fanconi_anemia": 1,
    "FANCG-related_disorder|Fanconi_anemia": 2,
    "not_provided|FANCG-related_disorder|Fanconi_anemia_complementation_group_G|Fanconi_anemia": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|FANCG-related_disorder": 1,
    "not_specified|Fanconi_anemia_complementation_group_G": 2,
    "Fanconi_anemia_complementation_group_G|not_specified|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases|Ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_G|not_specified|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_G|not_provided|Fanconi_anemia": 4,
    "Ovarian_cancer|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_G|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_G|not_provided": 2,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_G|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_G|Fanconi_anemia|Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_G|Fanconi_anemia": 3,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_G|not_provided": 1,
    "Fanconi_anemia_complementation_group_G|not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia|not_provided|not_specified": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|not_specified": 9,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 1,
    "FANCG-related_disorder|Fanconi_anemia_complementation_group_G|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_G|not_specified": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia|not_specified|not_provided|FANCG-related_disorder|Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Fanconi_anemia_complementation_group_G|not_specified|Fanconi_anemia|FANCG-related_disorder": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia|not_provided|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_G|not_specified": 1,
    "FANCG-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_G|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|FANCG-related_disorder": 1,
    "Abnormality_of_blood_and_blood-forming_tissues|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_G": 2,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_G|Inclusion_Body_Myopathy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Fanconi_anemia|not_specified|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_G": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia|not_provided|FANCG-related_disorder|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia_complementation_group_G|not_specified|Fanconi_anemia": 2,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_G": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia|Pituitary_stalk_interruption_syndrome|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia_complementation_group_G|Fanconi_anemia|not_specified": 1,
    "not_provided|FANCG-related_disorder|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia": 38,
    "FANCG-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 1,
    "Fanconi_anemia|not_specified|Ovarian_cancer": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_G": 1,
    "not_provided|Fanconi_anemia_complementation_group_G|not_specified": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2": 684,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 48,
    "PIGO-related_disorder|not_provided": 1,
    "PIGO-related_disorder|Intellectual_disability|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 1,
    "not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 15,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|PIGO-related_disorder|not_provided": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_specified|not_provided": 5,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_provided": 35,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 27,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|Inborn_genetic_diseases|not_provided": 5,
    "PIGO-related_disorder|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 3,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_provided|Inborn_genetic_diseases": 4,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|Inborn_genetic_diseases": 20,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_specified": 10,
    "not_provided|Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 4,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_specified|not_provided|PIGO-related_disorder": 1,
    "Hyperphosphatasia-intellectual_disability_syndrome|Hyperphosphatasia_with_intellectual_disability_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|PIGO-related_disorder|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 1,
    "PIGO-related_disorder|not_specified|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 2,
    "Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_provided": 3,
    "PIGO-related_disorder|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 3,
    "Inborn_genetic_diseases|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 4,
    "Inborn_genetic_diseases|Hyperphosphatasia-intellectual_disability_syndrome|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 1,
    "not_provided|not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 3,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_provided|PIGO-related_disorder": 2,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|PIGO-related_disorder|Hyperphosphatasia_with_intellectual_disability_syndrome_2": 1,
    "not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_2|not_provided": 1,
    "PIGO-related_disorder": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|PIGO-related_disorder|not_specified|not_provided": 2,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_2|Aganglionic_megacolon": 1,
    "UNC13B-related_seizure_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_61|not_provided": 11,
    "Intellectual_disability|_autosomal_recessive_61|not_provided|not_specified": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_61|not_specified": 3,
    "RUSC2-related_disorder": 2,
    "Intellectual_disability|_autosomal_recessive_61": 11,
    "not_provided|Intellectual_disability|_autosomal_recessive_61": 3,
    "not_provided|RUSC2-related_disorder": 5,
    "RUSC2-related_disorder|not_provided": 5,
    "Intellectual_disability|_autosomal_recessive_61|not_specified|not_provided": 4,
    "not_specified|Intellectual_disability|_autosomal_recessive_61|not_provided": 2,
    "not_specified|Intellectual_disability|_autosomal_recessive_61": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_61": 1,
    "Intellectual_disability|_autosomal_recessive_61|not_specified": 1,
    "RUSC2-related_disorder|Intellectual_disability|_autosomal_recessive_61|not_provided": 1,
    "not_provided|RUSC2-related_disorder|Intellectual_disability|_autosomal_recessive_61": 1,
    "Stuve-Wiedemann_syndrome_2|not_provided": 1,
    "Anauxetic_dysplasia": 411,
    "Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type": 82,
    "not_provided|Anauxetic_dysplasia": 3,
    "Anauxetic_dysplasia|not_specified|not_provided": 1,
    "not_specified|Anauxetic_dysplasia": 7,
    "Anauxetic_dysplasia|not_specified|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|RMRP-related_disorder": 2,
    "RMRP-related_disorder|Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "Anauxetic_dysplasia|not_provided|Metaphyseal_chondrodysplasia|_McKusick_type": 8,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia": 90,
    "not_specified|Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type": 3,
    "Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type": 3,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|not_specified": 6,
    "Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type": 63,
    "Metaphyseal_chondrodysplasia|_McKusick_type|not_specified": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|RMRP-related_disorder|Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|not_specified": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia_1|Anauxetic_dysplasia": 1,
    "Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|Anauxetic_dysplasia_1": 1,
    "Anauxetic_dysplasia|not_provided": 8,
    "Cartilage-Hair_Hypoplasia-Anauxetic_Dysplasia_Spectrum_Disorders|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 10,
    "Metaphyseal_dysplasia_without_hypotrichosis|not_provided|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia": 1,
    "Anauxetic_dysplasia|not_specified": 8,
    "not_specified|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "not_specified|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "Anauxetic_dysplasia|not_specified|not_provided|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Anauxetic_dysplasia|not_provided|not_specified|Metaphyseal_chondrodysplasia|_McKusick_type": 2,
    "Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|not_provided": 3,
    "Metaphyseal_chondrodysplasia|_McKusick_type|not_provided": 2,
    "not_provided|Cartilage-Hair_Hypoplasia-Anauxetic_Dysplasia_Spectrum_Disorders|Metaphyseal_chondrodysplasia|_McKusick_type|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia_1|Anauxetic_dysplasia": 1,
    "not_specified|Metaphyseal_chondrodysplasia|_McKusick_type|RMRP-related_disorder|Anauxetic_dysplasia|Metaphyseal_dysplasia_without_hypotrichosis|not_provided": 1,
    "RMRP-related_disorder|not_specified|Anauxetic_dysplasia|not_provided": 1,
    "Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type|Metaphyseal_dysplasia_without_hypotrichosis": 3,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "not_provided|Anauxetic_dysplasia|RMRP-related_disorder|Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type|Metaphyseal_dysplasia_without_hypotrichosis|not_specified": 1,
    "Anauxetic_dysplasia_1": 1,
    "not_specified|RMRP-related_disorder|Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "RMRP-related_disorder": 1,
    "Anauxetic_dysplasia|not_specified|Anauxetic_dysplasia_1": 1,
    "Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Anauxetic_dysplasia": 1,
    "Anauxetic_dysplasia|not_specified|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "not_specified|Anauxetic_dysplasia|RMRP-related_disorder": 1,
    "RMRP-related_disorder|Anauxetic_dysplasia": 2,
    "RMRP-related_disorder|Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|not_provided": 1,
    "Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type|not_provided": 2,
    "Metaphyseal_chondrodysplasia|_McKusick_type|RMRP-related_disorder|Anauxetic_dysplasia|not_specified": 1,
    "RMRP-related_disorder|Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|not_specified": 1,
    "Anauxetic_dysplasia|not_provided|RMRP-related_disorder": 1,
    "RMRP-related_disorder|Anauxetic_dysplasia|not_provided": 1,
    "Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis": 4,
    "not_specified|not_provided|Anauxetic_dysplasia": 1,
    "Anauxetic_dysplasia|Anauxetic_dysplasia_1": 1,
    "Anauxetic_dysplasia|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type|not_provided|RMRP-related_disorder": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia|Anauxetic_dysplasia_1": 1,
    "Anauxetic_dysplasia|not_specified|Cartilage-Hair_Hypoplasia-Anauxetic_Dysplasia_Spectrum_Disorders|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Anauxetic_dysplasia|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type": 5,
    "Metaphyseal_dysplasia_without_hypotrichosis": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia": 2,
    "not_specified|Anauxetic_dysplasia|RMRP-related_disorder|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "not_provided|Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Metaphyseal_chondrodysplasia|_McKusick_type|not_specified|Anauxetic_dysplasia": 1,
    "Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|not_provided": 2,
    "Anauxetic_dysplasia_1|Metaphyseal_chondrodysplasia|_McKusick_type|Metaphyseal_dysplasia_without_hypotrichosis|Anauxetic_dysplasia": 2,
    "RMRP-related_disorder|Anauxetic_dysplasia|not_specified|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Anauxetic_dysplasia|Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Anauxetic_dysplasia|not_specified|Metaphyseal_chondrodysplasia|_McKusick_type|not_provided": 1,
    "Anauxetic_dysplasia|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|Metaphyseal_chondrodysplasia|_McKusick_type|not_specified": 1,
    "Anauxetic_dysplasia|RMRP-related_disorder": 1,
    "Anauxetic_dysplasia|RMRP-related_disorder|Metaphyseal_chondrodysplasia|_McKusick_type": 1,
    "Anauxetic_dysplasia|not_specified|Metaphyseal_chondrodysplasia|_McKusick_type|not_provided|RMRP-related_disorder": 1,
    "Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|not_specified": 1,
    "Anauxetic_dysplasia|not_specified|Metaphyseal_chondrodysplasia|_McKusick_type|RMRP-related_disorder|not_provided": 1,
    "not_specified|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia": 1,
    "not_provided|not_specified|Anauxetic_dysplasia": 1,
    "Anauxetic_dysplasia|Metaphyseal_chondrodysplasia|_McKusick_type|Anauxetic_dysplasia_1|Metaphyseal_dysplasia_without_hypotrichosis|RMRP-related_disorder": 1,
    "Anauxetic_dysplasia|not_provided|not_specified": 1,
    "Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23|Distal_arthrogryposis_type_2B1": 1,
    "Congenital_myopathy_23": 6,
    "Congenital_myopathy_23|Arthrogryposis|_distal|_type_1A": 10,
    "Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23": 5,
    "not_provided|Congenital_myopathy_23|Arthrogryposis|_distal|_type_1A|not_specified": 1,
    "not_specified|not_provided|Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23": 1,
    "Arthrogryposis|_distal|_type_1A|not_provided": 14,
    "TPM2-related_disorder": 6,
    "Arthrogryposis|_distal|_type_1A": 151,
    "Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23|not_provided|TPM2-related_myopathy": 1,
    "Arthrogryposis_multiplex_congenita|not_specified|not_provided|Arthrogryposis|_distal|_type_1A|Nemaline_Myopathy|_Dominant": 1,
    "not_specified|Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Nemaline_Myopathy|_Dominant|not_specified|not_provided|Arthrogryposis_multiplex_congenita|TPM2-related_disorder|Arthrogryposis|_distal|_type_1A": 1,
    "Nemaline_Myopathy|_Dominant|Arthrogryposis_multiplex_congenita|not_specified|Arthrogryposis|_distal|_type_1A": 1,
    "not_provided|Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23": 4,
    "not_provided|Arthrogryposis|_distal|_type_1A": 7,
    "Arthrogryposis|_distal|_type_1A|not_specified": 4,
    "Arthrogryposis|_distal|_type_1A|Inborn_genetic_diseases": 2,
    "not_specified|Arthrogryposis|_distal|_type_1A|not_provided": 1,
    "Congenital_myopathy_23|not_provided": 1,
    "Congenital_myopathy_23|Arthrogryposis|_distal|_type_1A|not_specified|not_provided": 1,
    "not_specified|Arthrogryposis|_distal|_type_1A": 2,
    "Arthrogryposis|_distal|_type_1A|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy_23": 1,
    "not_specified|TPM2-related_disorder|Arthrogryposis|_distal|_type_1A": 1,
    "not_provided|TPM2-related_cap_myopathy|Arthrogryposis|_distal|_type_1A": 1,
    "not_provided|Congenital_myopathy_23|Arthrogryposis|_distal|_type_1A": 3,
    "Arthrogryposis|_distal|_type_1A|Inborn_genetic_diseases|not_provided": 3,
    "TPM2-related_disorder|not_provided|Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23": 1,
    "Arthrogryposis|not_provided|Arthrogryposis|_distal|_type_1A|TPM2-related_disorder|Arthrogryposis|_distal|_type_2B4": 1,
    "TPM2-related_disorder|Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B4": 1,
    "TPM2-related_disorder|Arthrogryposis|_distal|_type_1A": 1,
    "Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23|not_provided|Inborn_genetic_diseases": 1,
    "Arthrogryposis|_distal|_type_2B4": 1,
    "Distal_arthrogryposis_type_2B1": 24,
    "not_provided|Arthrogryposis|_distal|_type_1A|not_specified": 1,
    "not_provided|TPM2-related_disorder|Arthrogryposis|_distal|_type_1A": 1,
    "Inborn_genetic_diseases|Arthrogryposis|_distal|_type_1A": 1,
    "Congenital_myopathy_23|Arthrogryposis|_distal|_type_1A|not_provided": 1,
    "Arthrogryposis|_distal|_type_1A|TPM2-related_disorder": 2,
    "Arthrogryposis|_distal|_type_1A|Congenital_myopathy_23|not_provided": 2,
    "Congenital_myopathy_23|Arthrogryposis|_distal|_type_1A|TPM2-related_disorder|not_specified": 1,
    "Capillary_leak_syndrome": 1,
    "TLN1-related_disorder": 2,
    "Hereditary_spastic_paraplegia_46|Hereditary_spastic_paraplegia": 1,
    "Neurodevelopmental_disorder|Hereditary_spastic_paraplegia_46": 1,
    "Hereditary_spastic_paraplegia_46|not_provided": 1,
    "Spastic_paraplegia|GBA2-related_disorder": 1,
    "not_provided|Hereditary_spastic_paraplegia_46": 1,
    "Hereditary_spastic_paraplegia_46": 17,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia": 4,
    "Hereditary_spastic_paraplegia_46|GBA2-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|GBA2-related_disorder|not_provided": 1,
    "GBA2-related_disorder|Spastic_paraplegia": 1,
    "not_specified|GBA2-related_disorder|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_46|Hereditary_spastic_paraplegia|not_provided": 1,
    "Polyneuropathy|Primary_dilated_cardiomyopathy|Intellectual_disability|Spastic_paraparesis": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_46|not_provided|Spastic_paraplegia": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_46": 3,
    "Hereditary_spastic_paraplegia_46|Spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia_46|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|GBA2-related_disorder": 1,
    "Hereditary_spastic_paraplegia_5A|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraparesis|Cerebellar_ataxia|Primary_dilated_cardiomyopathy|Intellectual_disability|Polyneuropathy": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_46": 3,
    "Hereditary_spastic_paraplegia_46|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Spastic_paraplegia": 7,
    "not_provided|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|GBA2-related_disorder": 1,
    "Hereditary_spastic_paraplegia_46|Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_5A": 1,
    "Hereditary_spastic_paraplegia_46|CEP290-related_ciliopathy": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_46|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_46": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_46": 1,
    "not_specified|GBA2-related_disorder|Spastic_paraplegia": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia": 3,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 285,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type": 59,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_provided": 12,
    "NPR2-related_disorder|not_specified|Short_stature_with_nonspecific_skeletal_abnormalities_1|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|not_specified": 1,
    "not_provided|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type": 4,
    "Inborn_genetic_diseases|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 13,
    "Short_stature_with_nonspecific_skeletal_abnormalities": 6,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|Short_stature_with_nonspecific_skeletal_abnormalities|not_provided": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|not_provided": 3,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Short_stature_with_nonspecific_skeletal_abnormalities": 5,
    "not_provided|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 7,
    "not_specified|Inborn_genetic_diseases|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "not_provided|Short_stature_with_nonspecific_skeletal_abnormalities": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|not_provided|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 2,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|Inborn_genetic_diseases": 3,
    "Trident_hand|Growth_delay|Craniosynostosis_syndrome|Limb_undergrowth": 1,
    "NPR2-related_disorder|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "Short_stature_with_nonspecific_skeletal_abnormalities|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 4,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Inborn_genetic_diseases": 8,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|Short_stature_with_nonspecific_skeletal_abnormalities|Inborn_genetic_diseases|not_provided": 1,
    "NPR2-related_disorder": 3,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|not_provided": 3,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_provided|Short_stature_with_nonspecific_skeletal_abnormalities_1|not_specified": 1,
    "not_provided|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_specified": 1,
    "NPR2-related_disorder|Short_stature_with_nonspecific_skeletal_abnormalities|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_provided": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_specified": 4,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 5,
    "Short_stature_with_nonspecific_skeletal_abnormalities|Acromesomelic_dysplasia_1|_Maroteaux_type": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|NPR2-related_disorder|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_specified": 1,
    "not_provided|Acromesomelic_dysplasia_1|_Maroteaux_type|Short_stature_with_nonspecific_skeletal_abnormalities|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "NPR2-related_disorder|Inborn_genetic_diseases": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Short_stature_with_nonspecific_skeletal_abnormalities|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 2,
    "Disproportionate_short_stature": 1,
    "Short_stature_with_nonspecific_skeletal_abnormalities|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Short_stature_with_nonspecific_skeletal_abnormalities_1": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|NPR2-related_disorder": 3,
    "Inborn_genetic_diseases|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type": 3,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|not_provided|NPR2-related_disorder": 1,
    "not_specified|NPR2-related_disorder|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type": 1,
    "Short_stature_with_nonspecific_skeletal_abnormalities|not_provided|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 2,
    "Growth_delay|Trident_hand|Craniosynostosis_syndrome|Limb_undergrowth": 1,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Intellectual_disability": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|NPR2-related_disorder|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Short_stature_with_nonspecific_skeletal_abnormalities_1|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Short_stature_with_nonspecific_skeletal_abnormalities_1|Acromesomelic_dysplasia_1|_Maroteaux_type": 1,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|NPR2-related_disorder": 1,
    "Acromesomelic_dysplasia|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "not_specified|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type": 1,
    "Short_stature_with_nonspecific_skeletal_abnormalities|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|not_provided": 1,
    "not_provided|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|NPR2-related_disorder": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_2|Acromesomelic_dysplasia_1|_Maroteaux_type|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|NPR2-related_disorder|not_specified": 1,
    "Acromesomelic_dysplasia_1|_Maroteaux_type|Inborn_genetic_diseases|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_2|Acromesomelic_dysplasia_1|_Maroteaux_type": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_2|Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Acromesomelic_dysplasia_1|_Maroteaux_type|not_provided|NPR2-related_disorder": 1,
    "Tall_stature-scoliosis-macrodactyly_of_the_great_toes_syndrome|Short_stature_with_nonspecific_skeletal_abnormalities": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 180,
    "Spermatogenic_failure_91": 5,
    "Inclusion_Body_Myopathy|_Recessive|Sialuria|GNE_myopathy": 33,
    "Sialuria|GNE_myopathy": 358,
    "Inclusion_Body_Myopathy|_Recessive|Sialuria|GNE_myopathy|not_provided": 11,
    "Inclusion_Body_Myopathy|_Recessive|GNE_myopathy|Sialuria": 3,
    "GNE_myopathy|Sialuria": 247,
    "Inclusion_Body_Myopathy|_Recessive|GNE_myopathy|Sialuria|not_provided": 2,
    "not_provided|Sialuria|GNE_myopathy": 24,
    "Inclusion_Body_Myopathy|_Recessive|Sialuria|not_provided|GNE_myopathy": 5,
    "GNE_myopathy": 105,
    "GNE-related_disorder|GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy|Sialuria|not_provided": 1,
    "GNE_myopathy|Sialuria|not_provided": 30,
    "GNE-related_disorder|not_provided|Sialuria|GNE_myopathy": 1,
    "Inclusion_Body_Myopathy|_Recessive|GNE-related_disorder|Sialuria|GNE_myopathy|not_provided": 1,
    "Thrombocytopenia_12_with_or_without_myopathy|Sialuria|GNE_myopathy|GNE-related_disorder|not_provided": 1,
    "Sialuria|GNE_myopathy|not_provided": 39,
    "not_provided|GNE_myopathy|Sialuria": 24,
    "Inborn_genetic_diseases|GNE_myopathy|Sialuria": 3,
    "GNE_myopathy|not_provided|Sialuria": 3,
    "GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy|Sialuria|Myopathy|_autophagic_vacuolar|_infantile-onset|not_provided": 1,
    "not_provided|Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|Sialuria": 2,
    "not_specified|Sialuria|GNE_myopathy|not_provided": 2,
    "GNE-related_disorder": 6,
    "GNE-related_disorder|Sialuria|GNE_myopathy|not_provided|not_specified": 1,
    "GNE_myopathy|not_provided|Inborn_genetic_diseases|Sialuria": 1,
    "Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|Sialuria|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "not_provided|GNE_myopathy": 6,
    "GNE_myopathy|Sialuria|Inclusion_Body_Myopathy|_Recessive|not_specified|not_provided": 1,
    "Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|Sialuria": 6,
    "not_specified|Sialuria|GNE_myopathy": 7,
    "not_provided|GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy|Sialuria": 1,
    "Sialuria|GNE_myopathy|not_specified|Inclusion_Body_Myopathy|_Recessive|not_provided": 1,
    "Thrombocytopenia_12_with_or_without_myopathy|Sialuria|GNE_myopathy|not_provided": 2,
    "Sialuria": 3,
    "GNE_myopathy|not_provided": 10,
    "GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy|Sialuria|not_provided": 4,
    "Sialuria|GNE_myopathy|not_provided|Thrombocytopenia_12_with_or_without_myopathy": 1,
    "GNE_myopathy|Sialuria|not_specified|not_provided": 2,
    "GNE-related_disorder|Sialuria|GNE_myopathy|not_provided": 2,
    "Isolated_hereditary_giant_platelet_disorder|not_specified|GNE_myopathy|Sialuria": 1,
    "GNE_myopathy|Sialuria|not_specified": 2,
    "Sialuria|Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|not_provided": 1,
    "GNE_myopathy|Sialuria|Thrombocytopenia_12_with_or_without_myopathy|not_provided": 4,
    "not_specified|GNE_myopathy": 2,
    "GNE_myopathy|Sialuria|GNE-related_disorder|not_provided": 1,
    "Thrombocytopenia_12_with_or_without_myopathy": 1,
    "Sialuria|GNE_myopathy|not_specified": 3,
    "GNE_myopathy|Inborn_genetic_diseases|not_specified|not_provided|Sialuria": 1,
    "Inborn_genetic_diseases|Sialuria|GNE_myopathy": 1,
    "not_provided|GNE_myopathy|Sialuria|Inborn_genetic_diseases": 1,
    "GNE-related_disorder|Inclusion_Body_Myopathy|_Recessive|not_specified|Sialuria|GNE_myopathy|not_provided": 1,
    "Sialuria|GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy|not_provided": 1,
    "not_provided|Sialuria|GNE_myopathy|GNE-related_disorder": 1,
    "GNE_myopathy|not_specified|not_provided": 1,
    "Sialuria|GNE_myopathy|not_provided|not_specified": 1,
    "Sialuria|GNE_myopathy|not_specified|not_provided": 1,
    "Sialuria|GNE_myopathy|Inborn_genetic_diseases": 1,
    "Sialuria|Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Sialuria|Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy": 1,
    "GNE_myopathy|not_provided|Thrombocytopenia_12_with_or_without_myopathy|Sialuria": 1,
    "Sialuria|GNE_myopathy|GNE-related_disorder": 2,
    "GNE_myopathy|Sialuria|Thrombocytopenia_12_with_or_without_myopathy": 1,
    "GNE_myopathy|Sialuria|Inborn_genetic_diseases": 1,
    "GNE_myopathy|Sialuria|GNE-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Sialuria": 1,
    "not_specified|GNE_myopathy|Sialuria|not_provided": 1,
    "not_provided|GNE_myopathy|not_specified": 1,
    "Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|Sialuria|Myopathy|_autophagic_vacuolar|_infantile-onset|not_provided": 1,
    "Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy|Sialuria|not_provided": 1,
    "GNE-related_disorder|Sialuria|GNE_myopathy": 1,
    "not_specified|Sialuria|GNE_myopathy|not_provided|See_cases": 1,
    "Sialuria|GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy": 1,
    "Sialuria|GNE_myopathy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Sialuria|GNE_myopathy|not_specified|Inclusion_Body_Myopathy|_Recessive": 1,
    "Sialuria|GNE_myopathy|not_specified|Thrombocytopenia_12_with_or_without_myopathy|not_provided": 1,
    "GNE-related_disorder|Thrombocytopenia_12_with_or_without_myopathy|Sialuria|GNE_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|GNE_myopathy": 1,
    "Inborn_genetic_diseases|Sialuria|GNE_myopathy|not_provided": 1,
    "not_provided|Sialuria|GNE_myopathy|Thrombocytopenia": 1,
    "Sialuria|Thrombocytopenia_12_with_or_without_myopathy|GNE_myopathy": 1,
    "not_specified|GNE_myopathy|Sialuria": 1,
    "Sialuria|GNE_myopathy|not_provided|GNE-related_disorder": 1,
    "GNE_myopathy|Inclusion_Body_Myopathy|_Recessive|Sialuria": 2,
    "GNE_myopathy|Inclusion_body_myositis": 1,
    "not_specified|not_provided|Sialuria|GNE_myopathy": 1,
    "GNE_myopathy|Thrombocytopenia_12_with_or_without_myopathy|Sialuria": 1,
    "not_specified|not_provided|GNE_myopathy|Sialuria": 2,
    "not_provided|GNE_myopathy|Sialuria|Thrombocytopenia_12_with_or_without_myopathy": 1,
    "PAX5-related_disorder": 1,
    "not_specified|Leukemia|_acute_lymphoblastic|_susceptibility_to|_3": 1,
    "PAX5-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|PAX5-related_disorder": 1,
    "Leukemia|_acute_lymphoblastic|_susceptibility_to|_3|not_provided": 4,
    "Leukemia|_acute_lymphoblastic|_susceptibility_to|_3": 4,
    "Leukemia|_acute_lymphoblastic|_susceptibility_to|_3|not_specified": 1,
    "PAX5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|PAX5-related_disorder|not_provided|not_specified": 1,
    "not_provided|Leukemia|_acute_lymphoblastic|_susceptibility_to|_3": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|PAX5-related_disorder": 1,
    "Leukemia|_acute_lymphoblastic|_susceptibility_to|_3|Neurodevelopmental_disorder": 1,
    "Leukemia|_acute_lymphoblastic|_susceptibility_to|_3|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PAX5-related_disorder": 1,
    "Inborn_genetic_diseases|Leukemia|_acute_lymphoblastic|_susceptibility_to|_3": 1,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|Leukemia|_acute_lymphoblastic|_susceptibility_to|_3": 1,
    "not_provided|PAX5-related_disorder": 1,
    "Inborn_genetic_diseases|Leukemia|_acute_lymphoblastic|_susceptibility_to|_3|not_provided": 1,
    "Primary_hyperoxaluria|_type_II|not_provided": 39,
    "GRHPR-related_disorder": 3,
    "Primary_hyperoxaluria|_type_II": 154,
    "Nephrolithiasis/nephrocalcinosis|Primary_hyperoxaluria|_type_II": 2,
    "GRHPR-related_disorder|not_provided|Primary_hyperoxaluria|_type_II": 3,
    "Nephrolithiasis/nephrocalcinosis|Primary_hyperoxaluria|_type_II|not_provided": 3,
    "not_provided|Primary_hyperoxaluria|_type_II": 42,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Primary_hyperoxaluria|_type_II": 4,
    "Primary_hyperoxaluria|_type_II|Nephrolithiasis/nephrocalcinosis": 4,
    "Nephrolithiasis/nephrocalcinosis|not_provided": 12,
    "Nephrocalcinosis|Nephrolithiasis|not_provided|Primary_hyperoxaluria|_type_II": 1,
    "Primary_hyperoxaluria|_type_II|not_provided|Nephrolithiasis/nephrocalcinosis": 4,
    "not_provided|Primary_hyperoxaluria|_type_II|Nephrolithiasis/nephrocalcinosis": 3,
    "Primary_hyperoxaluria|_type_II|Nephrolithiasis/nephrocalcinosis|not_provided": 3,
    "Primary_hyperoxaluria|_type_II|not_provided|GRHPR-related_disorder": 1,
    "not_provided|Nephrolithiasis/nephrocalcinosis|Primary_hyperoxaluria|_type_II": 4,
    "not_specified|Primary_hyperoxaluria|_type_II": 4,
    "not_provided|GRHPR-related_disorder|Primary_hyperoxaluria|_type_II": 1,
    "Primary_hyperoxaluria|_type_II|not_specified|not_provided": 2,
    "Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_II": 1,
    "Nephrocalcinosis|Nephrolithiasis|Primary_hyperoxaluria|_type_II|not_provided": 1,
    "Primary_hyperoxaluria|_type_II|not_specified|not_provided|Nephrolithiasis/nephrocalcinosis": 1,
    "not_specified|not_provided|Primary_hyperoxaluria|_type_II": 2,
    "GRHPR-related_disorder|Primary_hyperoxaluria|not_provided|Primary_hyperoxaluria|_type_II": 1,
    "Primary_hyperoxaluria|_type_II|not_provided|not_specified": 1,
    "not_provided|Primary_hyperoxaluria|_type_II|Primary_hyperoxaluria": 1,
    "Pontocerebellar_hypoplasia_type_1B": 195,
    "not_provided|Pontocerebellar_hypoplasia_type_1B": 6,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1B|not_provided": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1B": 3,
    "Pontocerebellar_hypoplasia_type_1B|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|EXOSC3-related_disorder|not_provided|Pontocerebellar_hypoplasia_type_1B": 1,
    "Pontocerebellar_hypoplasia_type_1B|not_provided": 5,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_1B": 3,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_1B": 2,
    "Pontocerebellar_hypoplasia_type_1B|EXOSC3-related_disorder|not_provided": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_1B|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_1B|not_specified": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_1B": 1,
    "EXOSC3-related_disorder|Congenital_pontocerebellar_hypoplasia_type_1|Hypotonia|Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia_type_1B|Abnormality_of_the_nervous_system|See_cases": 1,
    "Pontocerebellar_hypoplasia_type_1B|not_specified": 4,
    "Pontocerebellar_hypoplasia_type_1B|Pontoneocerebellar_hypoplasia": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_1B|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_1B|EXOSC3-related_disorder": 1,
    "EXOSC3-related_disorder|not_provided|Pontocerebellar_hypoplasia_type_1B": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_1B|EXOSC3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|EXOSC3-related_disorder|Inborn_genetic_diseases|not_specified|Pontocerebellar_hypoplasia_type_1B": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Pontocerebellar_hypoplasia_type_1B": 2,
    "Microcephaly|Abnormal_cerebellum_morphology|Severe_intrauterine_growth_retardation|Hypoplasia_of_the_pons|Paucity_of_anterior_horn_motor_neurons|Lissencephaly|Fetal_akinesia_deformation_sequence_1|Congenital_myopathy|not_provided|Pontocerebellar_hypoplasia_type_1B": 1,
    "EXOSC3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia_type_1B": 2,
    "Inborn_genetic_diseases|not_specified|Pontocerebellar_hypoplasia_type_1B": 1,
    "PRKACG-related_disorder": 4,
    "PRKACG-related_disorder|not_specified": 1,
    "Platelet-type_bleeding_disorder_19": 1,
    "not_provided|Friedreich_ataxia_1|Friedreich_ataxia": 2,
    "Inborn_genetic_diseases|not_provided|Friedreich_ataxia_1": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Friedreich_ataxia_1": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Hypertrophic_cardiomyopathy|Friedreich_ataxia_1": 1,
    "not_provided|Friedreich_ataxia": 1,
    "Friedreich_ataxia_1": 8,
    "Friedreich_ataxia": 3,
    "Friedreich_ataxia_1|Friedreich_ataxia": 1,
    "Charcot-Marie-Tooth-like_disease|not_provided|FXN-related_disorder": 1,
    "FXN-related_disorder": 1,
    "not_provided|TJP2-related_disorder": 18,
    "TJP2-related_disorder|not_provided": 20,
    "TJP2-related_disorder|not_provided|not_specified": 5,
    "Cholestasis|_progressive_familial_intrahepatic|_4": 34,
    "Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1|not_provided": 1,
    "TJP2-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_4|Autosomal_dominant_nonsyndromic_hearing_loss_51|not_specified|not_provided|Hypercholanemia|_familial_1": 1,
    "not_specified|not_provided|Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1": 1,
    "TJP2-related_disorder": 24,
    "Inborn_genetic_diseases|not_provided|TJP2-related_disorder": 3,
    "Cholestasis|_progressive_familial_intrahepatic|_4|not_provided": 7,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_4": 4,
    "TJP2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Hypercholanemia|_familial_1|not_provided": 11,
    "Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1": 3,
    "Inborn_genetic_diseases|TJP2-related_disorder|not_provided": 2,
    "Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4|not_provided": 1,
    "not_provided|TJP2-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "not_provided|TJP2-related_disorder|Hypercholanemia|_familial_1": 1,
    "not_specified|not_provided|TJP2-related_disorder": 1,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1": 3,
    "TJP2-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "TJP2-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1|not_provided": 1,
    "TJP2-related_disorder|not_specified|not_provided": 4,
    "TJP2-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "not_provided|not_specified|Nonsyndromic_Hearing_Loss|_Dominant|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "TJP2-related_disorder|not_specified|not_provided|Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1": 1,
    "Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4": 2,
    "not_provided|not_specified|Cholestasis|_progressive_familial_intrahepatic|_4|Hypercholanemia|_familial_1": 1,
    "not_provided|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4": 2,
    "Inborn_genetic_diseases|TJP2-related_disorder": 1,
    "Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4|not_provided|Inborn_genetic_diseases": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant": 16,
    "not_provided|not_specified|TJP2-related_disorder": 2,
    "Hypercholanemia|_familial_1|not_provided|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "Melnick-Fraser_syndrome|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|not_provided|TJP2-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_51": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_4|not_specified|Hypercholanemia|_familial_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|TJP2-related_disorder|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_51": 1,
    "not_specified|Cholestasis|_progressive_familial_intrahepatic|_4|not_provided|Hypercholanemia|_familial_1": 1,
    "Inborn_genetic_diseases|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4|not_provided": 1,
    "not_provided|TJP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|TJP2-related_disorder|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_4|not_provided|Inborn_genetic_diseases": 1,
    "TJP2-related_disorder|not_provided|Hearing_impairment|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "Hypercholanemia|_familial_1|not_provided|not_specified|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "not_specified|not_provided|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_4|not_provided|TJP2-related_disorder": 1,
    "not_provided|Primary_biliary_cholangitis|TJP2-related_disorder|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "Inborn_genetic_diseases|not_provided|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4|TJP2-related_disorder": 1,
    "not_provided|TJP2-related_disorder|not_specified": 1,
    "not_provided|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4|not_specified": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|TJP2-related_disorder": 1,
    "TJP2-related_disorder|not_specified|Hypercholanemia|_familial_1|Cholestasis|_progressive_familial_intrahepatic|_4": 1,
    "Atelis_syndrome_2": 3,
    "Inborn_genetic_diseases|Intellectual_disability|Epileptic_encephalopathy": 1,
    "TRPM3-related_disorder": 36,
    "not_provided|TRPM3-related_disorder": 6,
    "Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skeletal_anomalies|_with_or_without_seizures": 12,
    "TRPM3-related_disorder|not_provided": 5,
    "Cataract_50_with_or_without_glaucoma": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skeletal_anomalies|_with_or_without_seizures|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skeletal_anomalies|_with_or_without_seizures|TRPM3-related_disorder|Birk-Barel_syndrome|Autosomal_dominant_non-syndromic_intellectual_disability|Inborn_genetic_diseases|Global_developmental_delay|Seizure|Mulibrey_nanism_syndrome|Intellectual_disability|not_provided": 1,
    "Inborn_genetic_diseases|Cataract_50_with_or_without_glaucoma|Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skeletal_anomalies|_with_or_without_seizures": 1,
    "TRPM3_related_neruodevelopmental_disorder": 1,
    "TRPM3-associated_epilepsy_syndrome": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skeletal_anomalies|_with_or_without_seizures": 2,
    "TRPM3-related_Intellectual_Disability_and_Epilepsy": 1,
    "Familial_progressive_retinal_dystrophy-iris_coloboma-congenital_cataract_syndrome|not_provided": 1,
    "MIR204-related_disorder|TRPM3-related_disorder|not_provided": 1,
    "Cataract_50_with_or_without_glaucoma|not_provided": 1,
    "Inguinal_hernia|Abnormal_sternum_morphology|Retinal_dystrophy|Joint_laxity|Hypertelorism|Myopia": 1,
    "Hypertelorism|Joint_laxity|Abnormal_sternum_morphology|Myopia|Retinal_dystrophy|Inguinal_hernia": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 13,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36": 20,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7": 74,
    "TMC1-related_disorder": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7": 2,
    "Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|Rare_genetic_deafness|not_provided|Hearing_loss|_autosomal_recessive|Ear_malformation": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 8,
    "Nonsyndromic_Hearing_Loss|_Dominant|not_specified|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|not_specified": 2,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "Inborn_genetic_diseases|TMC1-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "Intellectual_disability|_moderate|Bilateral_sensorineural_hearing_impairment|Delayed_speech_and_language_development": 1,
    "TMC1-related_disorder|not_provided": 4,
    "not_specified|TMC1-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Hearing_loss|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|TMC1-related_disorder|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Nonsyndromic_genetic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|Inborn_genetic_diseases|not_provided": 1,
    "TMC1-related_disorder|not_provided|Inborn_genetic_diseases|Monogenic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|Nonsyndromic_genetic_hearing_loss": 1,
    "Hearing_loss|_autosomal_recessive|Deafness|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided|Rare_genetic_deafness": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|Hearing_loss|_autosomal_recessive|Autosomal_dominant_nonsyndromic_hearing_loss_36|TMC1-related_disorder|Rare_genetic_deafness|not_provided": 1,
    "Hearing_impairment|Nonsyndromic_genetic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_36|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "not_provided|TMC1-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided": 5,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|TMC1-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|not_provided|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|Hearing_loss|_autosomal_recessive": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_7|Sensorineural_hearing_loss_disorder": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|not_specified": 1,
    "TMC1-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_7|Autosomal_dominant_nonsyndromic_hearing_loss_36": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7|not_provided|not_specified": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_36|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "not_specified|TMC1-related_disorder|not_provided": 1,
    "not_provided|ANXA1-related_disorder": 1,
    "ANXA1-related_disorder": 7,
    "RORB-related_disorder": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_15": 15,
    "RORB-related_disorder|Epilepsy|_idiopathic_generalized|_susceptibility_to|_15|not_provided": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_15": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_15|not_provided": 4,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_15|Epilepsy": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_15|Inborn_genetic_diseases": 2,
    "RORB-related_disorder|not_provided": 2,
    "not_provided|RORB-related_disorder": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_15|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Seizure|not_provided": 1,
    "Seizure|RORB-related_disorder": 1,
    "Intestinal_hypomagnesemia_1": 265,
    "not_provided|Intestinal_hypomagnesemia_1": 48,
    "Inborn_genetic_diseases|Intestinal_hypomagnesemia_1": 14,
    "not_specified|Intestinal_hypomagnesemia_1|not_provided": 2,
    "Intestinal_hypomagnesemia_1|Inborn_genetic_diseases|not_provided": 4,
    "Intestinal_hypomagnesemia_1|Inborn_genetic_diseases": 29,
    "Intestinal_hypomagnesemia_1|not_provided": 37,
    "Inborn_genetic_diseases|Intestinal_hypomagnesemia_1|not_provided": 5,
    "not_provided|TRPM6-related_disorder|Intestinal_hypomagnesemia_1": 2,
    "Inborn_genetic_diseases|not_provided|Intestinal_hypomagnesemia_1": 3,
    "not_provided|Inborn_genetic_diseases|Intestinal_hypomagnesemia_1": 2,
    "TRPM6-related_disorder|not_provided|Intestinal_hypomagnesemia_1": 2,
    "not_specified|not_provided|Intestinal_hypomagnesemia_1": 1,
    "Inborn_genetic_diseases|not_provided|TRPM6-related_disorder": 2,
    "TRPM6-related_disorder|Intestinal_hypomagnesemia_1|not_provided": 3,
    "not_provided|Intestinal_hypomagnesemia_1|TRPM6-related_disorder": 2,
    "Hypomagnesemia|Rod-cone_dystrophy|Abnormality_of_the_eye": 1,
    "Intestinal_hypomagnesemia_1|not_provided|Inborn_genetic_diseases": 1,
    "TRPM6-related_disorder": 4,
    "not_provided|Intestinal_hypomagnesemia_1|Inborn_genetic_diseases": 4,
    "not_provided|Hypomagnesemia": 1,
    "TRPM6-related_disorder|not_provided": 1,
    "PCSK5-related_disorder": 14,
    "not_provided|PCSK5-related_disorder": 2,
    "not_specified|PCSK5-related_disorder": 1,
    "Chorea-acanthocytosis": 354,
    "not_provided|Chorea-acanthocytosis": 139,
    "Chorea-acanthocytosis|not_provided": 141,
    "not_specified|Chorea-acanthocytosis": 3,
    "Chorea-acanthocytosis|Inborn_genetic_diseases": 12,
    "not_specified|not_provided|Chorea-acanthocytosis": 6,
    "Inborn_genetic_diseases|not_provided|Chorea-acanthocytosis": 9,
    "not_provided|VPS13A-related_disorder|Chorea-acanthocytosis": 2,
    "not_provided|Chorea-acanthocytosis|Inborn_genetic_diseases": 8,
    "VPS13A-related_disorder|not_provided|Chorea-acanthocytosis": 9,
    "not_provided|not_specified|VPS13A-related_disorder": 1,
    "VPS13A-related_disorder": 4,
    "Inborn_genetic_diseases|Chorea-acanthocytosis": 6,
    "Chorea-acanthocytosis|not_provided|not_specified": 1,
    "not_provided|Chorea-acanthocytosis|VPS13A-related_disorder": 5,
    "Chorea-acanthocytosis|not_specified|not_provided": 6,
    "Chorea-acanthocytosis|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "VPS13A-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Chorea-acanthocytosis|not_provided": 3,
    "not_provided|VPS13A-related_disorder": 6,
    "not_specified|Chorea-acanthocytosis|not_provided": 5,
    "VPS13A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Chorea-acanthocytosis": 5,
    "Chorea-acanthocytosis|VPS13A-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Chorea-acanthocytosis|not_provided|VPS13A-related_disorder": 1,
    "Chorea-acanthocytosis|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|VPS13A-related_disorder|Chorea-acanthocytosis": 1,
    "not_provided|Abnormality_of_the_nervous_system": 1,
    "Chorea-acanthocytosis|not_provided|Inborn_genetic_diseases": 4,
    "Chorea-acanthocytosis|not_provided|VPS13A-related_disorder": 2,
    "not_provided|VPS13A-related_disorder|not_specified|Chorea-acanthocytosis": 1,
    "not_provided|Chorea-acanthocytosis|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Chorea-acanthocytosis|VPS13A-related_disorder": 1,
    "not_specified|Chorea-acanthocytosis|VPS13A-related_disorder|not_provided": 1,
    "not_specified|Chorea-acanthocytosis|not_provided|Inborn_genetic_diseases": 1,
    "primray_hypomagnesemia_with_secondary_hypocalcemia": 1,
    "Chorea-acanthocytosis|Inborn_genetic_diseases|VPS13A-related_disorder|not_provided|not_specified": 1,
    "VPS13A-related_disorder|not_provided|not_specified": 1,
    "VPS13A-related_disorder|Chorea-acanthocytosis": 1,
    "not_specified|VPS13A-related_disorder|Chorea-acanthocytosis|not_provided": 1,
    "Cerebrofacial_arteriovenous_metameric_syndrome|not_specified": 1,
    "Kaposiform_hemangioendothelioma|Congenital_tufted_angioma|Pyogenic_granuloma|not_provided": 1,
    "Tufted_angioma_of_skin|not_specified": 1,
    "not_specified|GNA14-related_congenital_vascular_tumors": 1,
    "Tufted_angioma_of_skin": 1,
    "GNAQ-related_disorder": 4,
    "not_provided|Familial_multiple_nevi_flammei": 1,
    "Familial_multiple_nevi_flammei|not_provided": 1,
    "Sturge-Weber_syndrome": 1,
    "Abnormal_cardiovascular_system_morphology|Sturge-Weber_syndrome": 1,
    "Segmental_undergrowth_associated_with_capillary_malformation": 1,
    "GNAQ-related_disorder|Familial_multiple_nevi_flammei|Capillary_malformation|Melanoma|Sturge-Weber_syndrome|Angioosteohypertrophic_syndrome|Hemangiomatosis|Segmental_undergrowth_associated_with_capillary_malformation|not_provided": 1,
    "Familial_multiple_nevi_flammei": 2,
    "Sturge-Weber_syndrome|not_provided": 1,
    "Moyamoya_angiopathy|CEP78-related_disorder": 1,
    "CEP78-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|CEP78-related_disorder": 1,
    "Cone-rod_dystrophy_and_hearing_loss_1|not_provided": 5,
    "CEP78-related_disorder": 2,
    "not_provided|Cone-rod_dystrophy_and_hearing_loss_1": 7,
    "Cone-rod_dystrophy_and_hearing_loss_1|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_and_hearing_loss_1": 5,
    "Cone-rod_dystrophy_and_hearing_loss": 1,
    "Sensorineural_hearing_loss_disorder|Cone-rod_dystrophy|Cone-rod_dystrophy_and_hearing_loss_1|not_provided": 1,
    "CEP78-related_disorder|not_provided": 3,
    "Retinal_dystrophy|Cone-rod_dystrophy_and_hearing_loss_1": 2,
    "Sensorineural_hearing_loss_disorder|Cone-rod_dystrophy|Cone-rod_dystrophy_and_hearing_loss_1": 1,
    "not_provided|CEP78-related_disorder|not_specified": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_and_hearing_loss_1": 1,
    "Cone-rod_dystrophy_and_hearing_loss_1|Cone-rod_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_and_hearing_loss|not_provided|Cone-rod_dystrophy_and_hearing_loss_1": 1,
    "not_provided|CEP78-related_disorder": 3,
    "Cone-rod_dystrophy_and_hearing_loss_1|Retinal_dystrophy": 1,
    "not_specified|not_provided|CEP78-related_disorder|Cone-rod_dystrophy_and_hearing_loss_1": 1,
    "not_provided|not_specified|CEP78-related_disorder": 1,
    "CEP78-related_disorder|Retinal_dystrophy|not_specified|not_provided|Cone-rod_dystrophy_and_hearing_loss_1": 1,
    "PSAT_deficiency": 19,
    "not_provided|Neu-Laxova_syndrome_2|PSAT_deficiency": 3,
    "Neu-Laxova_syndrome_2|not_provided": 40,
    "PSAT_deficiency|Neu-Laxova_syndrome_2|not_provided": 6,
    "not_provided|Neu-Laxova_syndrome_2": 23,
    "Neu-Laxova_syndrome_2": 191,
    "Neu-Laxova_syndrome_2|not_provided|PSAT_deficiency|Microcephaly": 1,
    "PSAT_deficiency|not_provided": 4,
    "Neu-Laxova_syndrome_2|PSAT_deficiency": 8,
    "Neu-Laxova_syndrome_2|PSAT_deficiency|not_provided": 3,
    "PSAT1-related_disorder": 1,
    "PSAT_deficiency|Neu-Laxova_syndrome_2": 3,
    "Neu-Laxova_syndrome_2|not_provided|PSAT_deficiency": 4,
    "Neu-Laxova_syndrome_2|PSAT_deficiency|PSAT1-related_disorder": 1,
    "PSAT_deficiency|not_provided|PSAT1-related_disorder|Neu-Laxova_syndrome_2": 1,
    "PSAT1-related_disorder|not_provided|Neu-Laxova_syndrome_2": 1,
    "not_provided|Neu-Laxova_syndrome_2|High_myopia": 1,
    "PSAT1-related_disorder|PSAT_deficiency|Neu-Laxova_syndrome_2|not_provided": 2,
    "Neu-Laxova_syndrome_2|not_provided|PSAT_deficiency|PSAT1-related_disorder": 1,
    "Neu-Laxova_syndrome_2|PSAT1-related_disorder": 2,
    "PSAT1-related_disorder|Neu-Laxova_syndrome_2|PSAT_deficiency|not_provided": 1,
    "PSAT1-related_disorder|Neu-Laxova_syndrome_2": 2,
    "PSAT_deficiency|not_provided|Neu-Laxova_syndrome_2": 1,
    "PSAT1-related_disorder|not_provided|Neu-Laxova_syndrome_2|PSAT_deficiency": 1,
    "Neu-Laxova_syndrome_2|not_provided|PSAT1-related_disorder": 1,
    "Neu-Laxova_syndrome_2|PSAT1-related_disorder|not_provided": 1,
    "not_provided|PSAT_deficiency": 6,
    "not_provided|Neu-Laxova_syndrome_2|Neurometabolic_disorder_due_to_serine_deficiency": 1,
    "not_specified|RASEF-related_disorder": 1,
    "Preeclampsia|Normal_pregnancy|Small_for_gestational_age|Large_for_gestational_age": 1,
    "not_provided|Abnormal_brain_morphology": 3,
    "Au-Kline_syndrome|not_provided": 5,
    "Au-Kline_syndrome": 60,
    "not_provided|Au-Kline_syndrome": 2,
    "HNRNPK-related_disorder|not_provided": 1,
    "HNRNPK-related_disorder": 4,
    "not_provided|HNRNPK-related_disorder": 2,
    "Au-Kline_syndrome|Neonatal_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Au-Kline_syndrome": 2,
    "Au-Kline_syndrome|HNRNPK-related_disorder": 1,
    "Generalized_hypotonia": 4,
    "Inborn_genetic_diseases|Au-Kline_syndrome|not_provided": 1,
    "RMI1-related_disorder": 7,
    "RMI1-related_disorder|not_provided": 1,
    "NTRK2-related_disorder": 55,
    "Developmental_and_epileptic_encephalopathy|_58|Inborn_genetic_diseases|NTRK2-related_disorder|not_provided|Obesity|_hyperphagia|_and_developmental_delay": 1,
    "NTRK2-related_disorder|not_provided": 59,
    "NTRK2-related_disorder|not_provided|not_specified": 1,
    "not_provided|NTRK2-related_disorder": 51,
    "NTRK2-related_disorder|Developmental_and_epileptic_encephalopathy|_58": 1,
    "NTRK2-related_disorder|not_specified|not_provided": 2,
    "Obesity|_hyperphagia|_and_developmental_delay": 14,
    "Obesity|_hyperphagia|_and_developmental_delay|not_provided": 3,
    "not_provided|Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_58|Obesity|_hyperphagia|_and_developmental_delay": 3,
    "NTRK2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|NTRK2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|NTRK2-related_disorder": 4,
    "Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58|not_provided|Inborn_genetic_diseases|not_specified|NTRK2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_58": 4,
    "not_provided|not_specified|Inborn_genetic_diseases|NTRK2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|NTRK2-related_disorder": 1,
    "Inborn_genetic_diseases|NTRK2-related_disorder|not_provided": 1,
    "not_provided|NTRK2-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_58|Obesity|_hyperphagia|_and_developmental_delay": 1,
    "not_specified|not_provided|NTRK2-related_disorder": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_58|not_provided": 1,
    "Obesity|_hyperphagia|_and_developmental_delay|not_provided|NTRK2-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_58": 2,
    "Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58|Inborn_genetic_diseases|NTRK2-related_disorder|not_provided": 1,
    "Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58": 3,
    "Obesity|_hyperphagia|_and_developmental_delay|NTRK2-related_disorder": 1,
    "Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58|not_provided|NTRK2-related_disorder|Inborn_genetic_diseases": 1,
    "NTRK2-related_disorder|not_specified|Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58|not_provided": 1,
    "NTRK2-related_disorder|Obesity|_hyperphagia|_and_developmental_delay": 1,
    "NTRK2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_58|Obesity|_hyperphagia|_and_developmental_delay|not_specified": 1,
    "NTRK2-related_disorder|Obesity|_hyperphagia|_and_developmental_delay|not_provided": 1,
    "not_provided|Obesity|_hyperphagia|_and_developmental_delay": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_disorder|NTRK2-related_disorder": 1,
    "not_provided|Obesity|_hyperphagia|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_58|not_specified": 2,
    "AGTPBP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|AGTPBP1-related_disorder": 1,
    "AGTPBP1-related_disorder": 9,
    "Neurodegeneration|_childhood-onset|_with_cerebellar_atrophy": 26,
    "Global_developmental_delay|Aplasia/Hypoplasia_of_the_cerebellum|not_provided": 1,
    "Neurodegeneration|_childhood-onset|_with_cerebellar_atrophy|not_provided": 1,
    "Neurodegeneration|_childhood-onset|_with_cerebellar_atrophy|AGTPBP1-related_disorder": 2,
    "not_provided|Neurodegeneration|_childhood-onset|_with_cerebellar_atrophy": 3,
    "Neurodegeneration|_childhood-onset|_with_cerebellar_atrophy|Neurodevelopmental_disorder_with_cerebellar_atrophy_and_with_or_without_seizures": 1,
    "Global_developmental_delay|Aplasia/Hypoplasia_of_the_cerebellum": 1,
    "Global_developmental_delay|Motor_polyneuropathy|Aplasia/Hypoplasia_of_the_cerebellum": 1,
    "Neurodegeneration|_childhood-onset|_with_cerebellar_atrophy|Inborn_genetic_diseases": 1,
    "not_provided|AGTPBP1-related_disorder": 1,
    "Fatal_multiple_mitochondrial_dysfunctions_syndrome|Multiple_mitochondrial_dysfunctions_syndrome_5": 1,
    "ISCA1-related_disorder": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_5": 2,
    "not_provided|GAS1-related_disorder": 2,
    "Holoprosencephaly_1": 3,
    "GAS1-related_disorder|not_provided": 1,
    "GAS1-related_disorder": 4,
    "CDK20-related_disorder|not_provided": 4,
    "CDK20-related_disorder": 12,
    "Global_developmental_delay|Intellectual_disability|not_provided|Nephrotic_syndrome": 1,
    "Thyroid_hormone_metabolism|_abnormal_1": 11,
    "SECISBP2-related_disorder": 7,
    "Inborn_genetic_diseases|SECISBP2-related_disorder": 1,
    "SECISBP2-related_disorder|not_provided": 1,
    "Thyroid_hormone_metabolism|_abnormal_1|SECISBP2-related_disorder": 1,
    "not_provided|not_specified|SECISBP2-related_disorder": 1,
    "SEMA4D-related_disorder": 27,
    "not_provided|SEMA4D-related_disorder": 3,
    "SEMA4D-related_disorder|not_provided": 2,
    "not_specified|Anti-SEMA4D_Monoclonal_Antibody_VX15/2503": 1,
    "GADD45G-related_disorder": 4,
    "Immunodeficiency_82_with_systemic_inflammation": 7,
    "SYK-related_disorder": 2,
    "Immunodeficiency_82_with_systemic_inflammation|Decreased_circulating_immunoglobulin_concentration|Arthritis|Skin_rash|Colitis|Immunodeficiency": 2,
    "Arthritis|Skin_rash|Colitis|Immunodeficiency": 1,
    "Decreased_circulating_immunoglobulin_concentration|Arthritis|Skin_rash|Colitis|Immunodeficiency": 1,
    "Immunodeficiency_82_with_systemic_inflammation|not_provided|Decreased_circulating_immunoglobulin_concentration|Joint_swelling|Skin_rash|Colitis|Immunodeficiency": 1,
    "3-methylglutaconic_aciduria_type_1": 147,
    "3-methylglutaconic_aciduria_type_1|not_provided": 9,
    "not_provided|3-methylglutaconic_aciduria_type_1": 7,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_1|not_provided": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_1": 6,
    "3-methylglutaconic_aciduria_type_1|Inborn_genetic_diseases": 10,
    "3-methylglutaconic_aciduria_type_1|not_specified": 5,
    "3-methylglutaconic_aciduria_type_1|AUH-related_disorder": 1,
    "not_specified|not_provided|3-methylglutaconic_aciduria_type_1": 4,
    "not_specified|3-methylglutaconic_aciduria_type_1|not_provided": 1,
    "not_provided|3-Methylglutaconic_aciduria": 1,
    "not_provided|Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_1": 1,
    "not_specified|3-methylglutaconic_aciduria_type_1": 2,
    "Inborn_genetic_diseases|not_provided|3-methylglutaconic_aciduria_type_1": 2,
    "not_provided|3-methylglutaconic_aciduria_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|AUH-related_disorder|3-methylglutaconic_aciduria_type_1": 1,
    "AUH-related_disorder|not_specified|3-methylglutaconic_aciduria_type_1": 1,
    "AUH-related_disorder|not_provided": 1,
    "3-methylglutaconic_aciduria_type_1|not_provided|not_specified": 1,
    "not_provided|3-methylglutaconic_aciduria_type_1|not_specified": 2,
    "AUH-related_disorder|3-methylglutaconic_aciduria_type_1|not_provided": 1,
    "not_provided|3-methylglutaconic_aciduria_type_1|AUH-related_disorder": 1,
    "Inborn_genetic_diseases|AUH-related_disorder|not_provided|3-methylglutaconic_aciduria_type_1": 1,
    "NFIL3-related_disorder|not_provided": 1,
    "NFIL3-related_disorder": 1,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided": 14,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 29,
    "Brachydactyly|Autosomal_dominant_Robinow_syndrome_1": 1,
    "Brachydactyly_type_B1|not_provided|Autosomal_recessive_Robinow_syndrome": 4,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_provided": 15,
    "not_provided|Autosomal_dominant_Robinow_syndrome_1|Brachydactyly": 1,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 91,
    "not_provided|not_specified|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 1,
    "not_specified|not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 4,
    "not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 31,
    "not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|Inborn_genetic_diseases": 9,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|Inborn_genetic_diseases|not_provided": 4,
    "ROR2-related_disorder": 5,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided": 1,
    "ROR2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 31,
    "ROR2-related_disorder|not_provided": 3,
    "not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_specified": 1,
    "Brachydactyly_type_B1|Short_stature": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 4,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 3,
    "not_specified|not_provided|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 6,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided|Autosomal_dominant_Robinow_syndrome_1|not_specified": 1,
    "not_provided|ROR2-related_disorder": 6,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "ROR2-related_disorder|not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 1,
    "Autosomal_recessive_Robinow_syndrome": 28,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1": 6,
    "Distal_symphalangism|not_provided|Brachydactyly_type_B1": 1,
    "Brachydactyly|_type_B1Robinow_syndrome|_autosomal_recessive|not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 1,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_provided|not_specified": 1,
    "not_provided|Brachydactyly_type_B1": 2,
    "Brachydactyly_type_B1|not_provided": 1,
    "Brachydactyly_type_B1": 8,
    "Inborn_genetic_diseases|not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 6,
    "not_provided|Autosomal_recessive_Robinow_syndrome": 3,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|Short_stature|not_provided|ROR2-related_disorder": 1,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided|not_specified": 4,
    "Autosomal_recessive_Robinow_syndrome|not_provided|not_specified|Brachydactyly_type_B1": 2,
    "Autosomal_recessive_Robinow_syndrome|not_provided|Brachydactyly_type_B1": 4,
    "Cleft_lip": 1,
    "not_provided|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|Short_stature|Intellectual_disability": 1,
    "Autosomal_recessive_Robinow_syndrome|not_provided|Brachydactyly_type_B1|Brachydactyly|_type_B1Robinow_syndrome|_autosomal_recessive": 1,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_provided|ROR2-related_disorder": 3,
    "Inborn_genetic_diseases|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_Robinow_syndrome": 1,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided|Inborn_genetic_diseases": 2,
    "ROR2-related_disorder|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided": 1,
    "Autosomal_recessive_Robinow_syndrome|not_provided|ROR2-related_disorder|Brachydactyly_type_B1": 2,
    "not_provided|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_Robinow_syndrome|not_specified|not_provided|ROR2-related_disorder|Brachydactyly_type_B1": 1,
    "not_provided|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_specified|Short_stature|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "not_provided|Inborn_genetic_diseases|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 2,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|ROR2-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_Robinow_syndrome|ROR2-related_disorder|Brachydactyly_type_B1": 1,
    "not_specified|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|Inborn_genetic_diseases|not_provided": 1,
    "Brachydactyly_type_B1|Robinow_syndrome|_autosomal_recessive|_with_aplasia/hypoplasia_of_phalanges_and_metacarpals/metatarsals": 1,
    "Robinow_syndrome|_autosomal_recessive|_with_brachy-syn-polydactyly|Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided": 1,
    "Autosomal_recessive_Robinow_syndrome|not_provided|Brachydactyly_type_B1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 3,
    "Autosomal_recessive_Robinow_syndrome|not_provided|Brachydactyly_type_B1|not_specified": 1,
    "Autosomal_recessive_Robinow_syndrome|Brachydactyly_type_B1|not_provided|ROR2-related_disorder": 1,
    "Autosomal_recessive_Robinow_syndrome|Short_stature|not_provided|ROR2-related_disorder|Brachydactyly_type_B1": 1,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_specified": 1,
    "not_provided|ROR2-related_disorder|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 1,
    "Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|not_provided": 2,
    "Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome|not_provided|Short_stature": 2,
    "Brachydactyly_type_B1|not_provided|ROR2-related_disorder|Autosomal_recessive_Robinow_syndrome": 1,
    "Autosomal_recessive_Robinow_syndrome|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_Robinow_syndrome|not_provided": 1,
    "not_provided|ROR2-related_disorder|Inborn_genetic_diseases|Brachydactyly_type_B1|Autosomal_recessive_Robinow_syndrome": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 27,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_27|_juvenile": 3,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1": 279,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Charcot-Marie-Tooth_disease|not_specified|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|Amyotrophic_lateral_sclerosis_27|_juvenile|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1": 4,
    "Childhood_onset_hearing_loss|Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|not_provided": 4,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases": 11,
    "Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 10,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_1": 4,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases|not_provided|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Amyotrophic_lateral_sclerosis_27|_juvenile|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Amyotrophic_lateral_sclerosis_27|_juvenile": 3,
    "SPTLC1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 3,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Hereditary_sensory_and_autonomic_neuropathy_type_1": 3,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 6,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1": 10,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_1|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 2,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_IA|_severe|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_27|_juvenile|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_IA|_severe": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Inborn_genetic_diseases|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|SPTLC1-related_disorder|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_sensory_and_autonomic_neuropathy_type_1|SPTLC1-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis|Hereditary_sensory_and_autonomic_neuropathy_type_1|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified|not_provided": 1,
    "not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|SPTLC1-related_disorder|not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified": 3,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "not_specified|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Charcot-Marie-Tooth_disease": 1,
    "SPTLC1-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "SPTLC1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Charcot-Marie-Tooth_disease|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|Sensorimotor_neuropathy": 1,
    "Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_1|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|SPTLC1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_27|_juvenile": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Amyotrophic_lateral_sclerosis_27|_juvenile|Muscle_spasm|EMG_abnormality|Proximal_muscle_weakness|Falls|Proximal_lower_limb_amyotrophy|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_1": 1,
    "Amyotrophic_lateral_sclerosis_27|_juvenile|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A": 1,
    "Amyotrophic_lateral_sclerosis_27|_juvenile|Ritscher-Schinzel_syndrome_4|Neuropathy|_hereditary_sensory_and_autonomic|_type_1A|not_provided": 1,
    "IARS1-related_disorder|not_provided": 5,
    "Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy": 21,
    "Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy|not_specified|not_provided": 2,
    "IARS1-related_disorder": 5,
    "Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy|IARS1-related_disorder|not_provided": 1,
    "not_provided|Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy|not_specified": 1,
    "IARS1-related_disorder|not_specified|not_provided": 1,
    "Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy|not_specified": 3,
    "not_provided|IARS1-related_disorder": 9,
    "not_provided|not_specified|Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy": 2,
    "Microcephaly|Global_developmental_delay": 2,
    "not_specified|Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy": 2,
    "not_specified|IARS1-related_disorder": 1,
    "Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy|not_provided": 2,
    "not_provided|Growth_retardation|_intellectual_developmental_disorder|_hypotonia|_and_hepatopathy": 1,
    "CENPP-related_disorder": 4,
    "ASPN-related_disorder": 5,
    "CENPP-related_disorder|not_specified|Osteoarthritis_susceptibility_3|Lumbar_disk_degeneration|_susceptibility_to": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 526,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases": 48,
    "BICD2-related_disorder|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 5,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified": 9,
    "Spastic_paraplegia|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "BICD2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 37,
    "BICD2-related_disorder|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided": 20,
    "not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 19,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 8,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome": 1,
    "BICD2-related_disorder": 8,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases|BICD2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 4,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 2,
    "not_provided|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified": 5,
    "not_specified|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 1,
    "not_specified|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided": 2,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided|Inborn_genetic_diseases": 5,
    "not_provided|Myopathy|Pelvic_girdle_muscle_weakness|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 6,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases|BICD2-related_disorder": 1,
    "BICD2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Spinal_muscular_atrophy_with_lower_extremity_predominance": 1,
    "Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant|not_provided": 1,
    "Spinal_muscular_atrophy|_lower_extremity-predominant|_2|_AD|Autosomal_dominant_hereditary_axonal_motor_and_sensory_neuropathy|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Charcot-Marie-Tooth_disease|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided|BICD2-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided": 7,
    "not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases": 3,
    "Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 2,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "BICD2-related_disorder|Hereditary_spastic_paraplegia_3A|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "BICD2-related_disorder|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|BICD2-related_disorder": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Neuronopathy|_distal_hereditary_motor|_type_5B|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|BICD2-related_disorder": 3,
    "Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant|not_provided|Inborn_genetic_diseases|Tapered_finger|Feeding_difficulties|EEG_abnormality|Macrocephaly|Recurrent_fractures|Muscular_atrophy|Downturned_corners_of_mouth|Arthrogryposis_multiplex_congenita|Cerebral_cortical_atrophy|Decreased_fetal_movement|Open_mouth|Muscle_weakness|Absent_speech|Seizure": 1,
    "Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 4,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided": 1,
    "Hereditary_spastic_paraplegia_3A|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Inborn_genetic_diseases|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 1,
    "BICD2-related_disorder|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 1,
    "not_specified|BICD2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|BICD2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified|BICD2-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|BICD2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|BICD2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Spinal_muscular_atrophy|_lower_extremity-predominant|_2b|_prenatal_onset|_autosomal_dominant": 1,
    "not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Inborn_genetic_diseases|BICD2-related_disorder": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Hereditary_spastic_paraplegia|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|Spastic_paraplegia": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 2,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified|BICD2-related_disorder": 1,
    "not_provided|not_specified|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures": 1,
    "BICD2-related_Autosomal_recessive_Cohen_Like_syndrome": 1,
    "Spinal_muscular_atrophy|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_provided|Distal_myopathy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "BICD2-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_with_contractures|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "WNK2-related_condition": 1,
    "Hypotonia|Hyperactive_airways|Bilateral_undescended_testicles|Chronic_lung_disease|Coarse_facial_features|Scoliosis|Cutis_laxa|Pectus_excavatum|Gastroesophageal_reflux": 1,
    "PHF2-related_disorder": 15,
    "PHF2-related_disorder|not_provided": 2,
    "not_provided|not_specified|PHF2-related_disorder": 1,
    "not_provided|PHF2-related_disorder": 1,
    "Leukodystrophy|_childhood-onset|_remitting|not_provided": 1,
    "Leukodystrophy|_childhood-onset|_remitting": 1,
    "not_provided|Fructose-biphosphatase_deficiency": 13,
    "Fructose-biphosphatase_deficiency": 227,
    "Fructose-biphosphatase_deficiency|not_specified|not_provided": 3,
    "FBP1-related_disorder": 1,
    "not_provided|not_specified|Fructose-biphosphatase_deficiency": 5,
    "Inborn_genetic_diseases|not_provided|Fructose-biphosphatase_deficiency": 2,
    "Fructose-biphosphatase_deficiency|not_provided|not_specified": 1,
    "Fructose-biphosphatase_deficiency|FBP1-related_disorder|not_provided": 1,
    "Fructose-biphosphatase_deficiency|Inborn_genetic_diseases": 3,
    "not_provided|Fructose-biphosphatase_deficiency|not_specified": 3,
    "not_provided|Fructose-biphosphatase_deficiency|FBP1-related_disorder": 1,
    "not_specified|not_provided|FBP1-related_disorder|Fructose-biphosphatase_deficiency": 1,
    "Fructose-biphosphatase_deficiency|not_specified": 7,
    "not_specified|Fructose-biphosphatase_deficiency": 7,
    "FBP1-related_disorder|Fructose-biphosphatase_deficiency": 2,
    "not_provided|FBP1-related_disorder|Fructose-biphosphatase_deficiency": 1,
    "Inborn_genetic_diseases|Fructose-biphosphatase_deficiency": 2,
    "Deficiency_of_fructose-bisphosphatase": 1,
    "Fructose-biphosphatase_deficiency|not_provided": 3,
    "Abnormality_of_acid-base_homeostasis|Impaired_gluconeogenesis": 1,
    "Dystonia_31": 10,
    "AOPEP-related_disorder|Dystonia_31": 1,
    "not_provided|Fanconi_anemia_complementation_group_C": 7,
    "Fanconi_anemia_complementation_group_C|not_provided": 6,
    "Fanconi_anemia_complementation_group_C|not_specified": 4,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia|FANCC-related_disorder|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Malignant_tumor_of_breast": 3,
    "FANCC-related_disorder": 7,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C": 14,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 19,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 16,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 13,
    "FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 3,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia": 25,
    "not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 145,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 15,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 6,
    "not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 4,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_provided|FANCC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided": 17,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_A": 2,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|FANCC-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|Fanconi_anemia": 13,
    "Fanconi_anemia_complementation_group_C|not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_C|FANCC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|Fanconi_anemia": 3,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 7,
    "not_provided|Fanconi_anemia_complementation_group_C|not_specified|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_C|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|Malignant_tumor_of_breast|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C": 22,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 13,
    "not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 13,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia": 3,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_specified": 3,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 8,
    "FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "FANCC-related_disorder|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 9,
    "FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C": 8,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_provided|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C": 5,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C|FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_C": 5,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 6,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 14,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Fanconi_anemia_complementation_group_A|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|FANCC-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 2,
    "Hereditary_cancer|FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_provided": 2,
    "not_specified|Fanconi_anemia|not_provided|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_specified": 2,
    "Fanconi_anemia|Malignant_tumor_of_breast": 2,
    "FANCC-related_disorder|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_C|not_specified|FANCC-related_disorder": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "FANCC-related_disorder|Fanconi_anemia|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C|not_specified": 1,
    "Fanconi_anemia_complementation_group_C|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 3,
    "Fanconi_anemia|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia|FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 4,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 6,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C": 2,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "Fanconi_anemia|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_provided|FANCC-related_disorder": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Malignant_tumor_of_breast|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_provided": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified": 10,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "FANCC-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_A|Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_A|not_specified|not_provided|Fanconi_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|Fanconi_anemia|not_provided": 5,
    "Malignant_tumor_of_breast|Fanconi_anemia": 3,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_C|not_provided": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_provided": 2,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_A": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_provided|Fanconi_anemia": 5,
    "not_specified|Fanconi_anemia|FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Premature_ovarian_failure": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Malignant_tumor_of_breast": 2,
    "not_provided|X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement": 3,
    "X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement": 28,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 3,
    "not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C": 2,
    "not_specified|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 2,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 3,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_C": 5,
    "Fanconi_anemia_complementation_group_C|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 2,
    "not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified|FANCC-related_disorder|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_provided|FANCC-related_disorder|Hereditary_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_C|Fanconi_anemia|FANCC-related_disorder": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|FANCC-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_C|not_specified|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCC-related_disorder|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "FANCC-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "FANCC-related_disorder|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_C|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 3,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast|Fanconi_anemia|Hereditary_cancer": 1,
    "FANCC-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_specified|Malignant_tumor_of_breast|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Fanconi_anemia|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia": 2,
    "FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|not_specified": 3,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia_complementation_group_C|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 4,
    "Fanconi_anemia|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_provided|not_specified|Fanconi_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Malignant_tumor_of_breast": 1,
    "FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Fanconi_anemia_complementation_group_A|Malignant_tumor_of_breast": 2,
    "Fanconi_anemia_complementation_group_C|Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_C|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Fanconi_anemia_complementation_group_A|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_C|Fanconi_anemia|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|Fanconi_anemia|not_specified|not_provided": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Fanconi_anemia_complementation_group_A": 1,
    "FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|FANCC-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|FANCC-related_disorder": 1,
    "not_provided|Fanconi_anemia_complementation_group_A": 17,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_ovarian_cancer|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|FANCC-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|not_specified|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia_complementation_group_C|not_specified|Fanconi_anemia": 3,
    "not_provided|not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Malignant_tumor_of_breast|not_specified|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|FANCC-related_disorder|not_provided|Fanconi_anemia_complementation_group_C": 1,
    "not_provided|Fanconi_anemia_complementation_group_C|FANCC-related_disorder|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|FANCC-related_disorder": 1,
    "not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer": 1,
    "Fanconi_anemia|not_specified|not_provided": 2,
    "not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Fanconi_anemia_complementation_group_C|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "FANCC-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_C|Malignant_tumor_of_breast": 1,
    "FANCC-related_disorder|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|not_specified": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 12,
    "Fanconi_anemia_complementation_group_C|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_C|Fanconi_anemia_complementation_group_A|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_C|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|not_provided": 1,
    "not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|FANCC-related_disorder": 1,
    "Malignant_tumor_of_breast|not_specified|Hereditary_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_C|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "FANCC-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_provided|not_specified": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_C|not_provided": 1,
    "not_provided|FANCC-related_disorder|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_C": 1,
    "FANCC-related_disorder|not_specified": 1,
    "not_provided|Fanconi_anemia_complementation_group_C|not_specified": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_C|not_specified": 1,
    "not_provided|Holoprosencephaly_7|Gorlin_syndrome": 3,
    "Holoprosencephaly_7|Gorlin_syndrome": 36,
    "Holoprosencephaly_7|not_provided|Gorlin_syndrome": 3,
    "Holoprosencephaly_7|Gorlin_syndrome|not_provided": 11,
    "Holoprosencephaly_sequence|Gorlin_syndrome": 5,
    "Gorlin_syndrome|Holoprosencephaly_7": 28,
    "not_provided|Holoprosencephaly_sequence|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Holoprosencephaly_sequence|not_provided": 1,
    "Gorlin_syndrome|not_provided|Holoprosencephaly_7": 1,
    "not_provided|Gorlin_syndrome|Holoprosencephaly_sequence": 1,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|PTCH1-related_disorder|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 766,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 664,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 45,
    "Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "Holoprosencephaly_7|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 37,
    "Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 30,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1": 14,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 72,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|Gorlin_syndrome|not_specified": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 2,
    "Gorlin_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "PTCH1-related_disorder|not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided": 34,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Gorlin_syndrome|not_provided|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 11,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Holoprosencephaly_7|not_provided|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 11,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 10,
    "not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 45,
    "Gorlin_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|not_provided|Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|Gorlin_syndrome": 4,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1": 12,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 14,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified": 9,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "not_specified|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "not_provided|Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|Gorlin_syndrome|not_specified|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Holoprosencephaly_7|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome|not_provided|Holoprosencephaly_7": 2,
    "PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 13,
    "Hereditary_cancer|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 3,
    "PTCH1-related_disorder": 22,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 2,
    "not_specified|PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Gorlin_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 6,
    "Gorlin_syndrome|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|PTCH1-related_disorder": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 2,
    "PTCH1-related_disorder|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "not_provided|PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Intellectual_disability|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Holoprosencephaly_7|not_specified|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 2,
    "Gorlin_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|PTCH1-related_disorder|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 3,
    "Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome|Rieger_anomaly|Irido-corneo-trabecular_dysgenesis|PTCH1-related_disorder": 1,
    "not_provided|Turner_syndrome|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|PTCH1-related_disorder": 8,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|not_provided|Pituitary_stalk_interruption_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7": 3,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified|not_provided|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1": 2,
    "PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|not_provided|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Rieger_anomaly|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Gorlin_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 7,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 4,
    "Gorlin_syndrome|not_specified|Holoprosencephaly_7|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Ovarian_cancer|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma": 1,
    "not_provided|not_specified|Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "not_specified|not_provided|Gorlin_syndrome": 2,
    "PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 4,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|PTCH1-related_disorder|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|See_cases|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_nevus_syndrome_1|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided|Basal_cell_nevus_syndrome_1": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|not_provided": 1,
    "PTCH1-related_disorder|Gorlin_syndrome|not_specified|Fraser_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|not_specified": 1,
    "Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_7|Polydactyly_of_a_triphalangeal_thumb|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "Holoprosencephaly_7|not_specified|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Holoprosencephaly_7|not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|not_specified": 1,
    "not_provided|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Holoprosencephaly_7|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|not_specified": 1,
    "not_provided|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gorlin_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7": 1,
    "Cataract|Disproportionate_tall_stature|Abnormal_cardiovascular_system_morphology|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Holoprosencephaly_7|Gorlin_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder": 4,
    "not_provided|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Gorlin_syndrome|PTCH1-related_disorder": 2,
    "Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Holoprosencephaly_7|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gorlin_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided": 1,
    "Ovarian_cancer|Gorlin_syndrome|not_provided|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Anophthalmia-microphthalmia_syndrome|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "not_provided|Holoprosencephaly_7|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Anophthalmia-microphthalmia_syndrome|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 1,
    "Gorlin_syndrome|PTCH1-related_disorder": 3,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_sequence|Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|not_provided": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome": 2,
    "Gorlin_syndrome|Inborn_genetic_diseases": 3,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_skin_disorder": 1,
    "not_provided|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Congenital_heart_disease|Gorlin_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Holoprosencephaly_7|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "See_cases|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 5,
    "Basal_cell_nevus_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Basal_cell_nevus_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Irido-corneo-trabecular_dysgenesis|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 2,
    "Holoprosencephaly_7|Gorlin_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Basal_cell_nevus_syndrome_1": 1,
    "Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "Basal_cell_nevus_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified": 1,
    "Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Gorlin_syndrome|not_provided|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Microform_holoprosencephaly|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_7|Gorlin_syndrome": 4,
    "Gorlin_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|PTCH1-related_disorder": 1,
    "Holoprosencephaly_sequence|not_specified|Gorlin_syndrome|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Basal_cell_nevus_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7": 2,
    "Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "PTCH1-related_disorder|Precocious_puberty|Postaxial_polydactyly|Macrocephaly|Overgrowth": 1,
    "Autism_spectrum_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Medulloblastoma|Gorlin_syndrome": 226,
    "Gorlin_syndrome|not_provided|Holoprosencephaly_7|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|not_provided|Gorlin_syndrome|not_specified": 1,
    "Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome|not_provided": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|not_specified": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7": 1,
    "Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided": 1,
    "Gorlin_syndrome|PTCH1-related_disorder|Basal_cell_nevus_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Holoprosencephaly_7|Acute_myeloid_leukemia|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|Basal_cell_nevus_syndrome_1": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Congenital_hydrocephalus": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided|Holoprosencephaly_7": 2,
    "Basal_cell_nevus_syndrome_1|Holoprosencephaly_7": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "not_specified|Gorlin_syndrome|not_provided|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|See_cases|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Gorlin_syndrome|not_provided": 1,
    "Holoprosencephaly_7|not_provided|not_specified|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|not_specified|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 3,
    "not_specified|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome|not_specified|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1": 1,
    "4-5_toe_syndactyly|Abnormal_eye_morphology|Basal_cell_nevi": 1,
    "Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Holoprosencephaly_7": 1,
    "not_specified|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Gorlin_syndrome|not_provided|PTCH1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|Gorlin_syndrome|not_provided": 1,
    "not_provided|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Holoprosencephaly_sequence|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|not_specified|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Holoprosencephaly_7|not_provided|Gorlin_syndrome": 1,
    "PTCH1-related_disorder|Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|not_provided|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Holoprosencephaly_7|Gorlin_syndrome|not_provided|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Craniosynostosis_syndrome|not_provided": 1,
    "not_provided|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Anophthalmia-microphthalmia_syndrome|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Holoprosencephaly_7|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7": 1,
    "Myopia|Intellectual_disability|Lens_luxation|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 1,
    "not_provided|Gorlin_syndrome|PTCH1-related_disorder|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gorlin_syndrome|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided|Germinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Holoprosencephaly_7|Gorlin_syndrome|Intellectual_disability|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|not_specified|Holoprosencephaly_7": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1": 2,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|not_provided": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_nevus_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Craniosynostosis_syndrome|not_provided|Gorlin_syndrome": 1,
    "PTCH1-related_disorder|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_specified|not_provided|Basal_cell_nevus_syndrome_1": 1,
    "not_specified|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided|Basal_cell_nevus_syndrome_1": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided": 1,
    "PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Gorlin_syndrome|Retinoblastoma|PTCH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided|not_specified": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7": 1,
    "PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7": 1,
    "See_cases|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|Gorlin_syndrome|Holoprosencephaly_7|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Holoprosencephaly_7|not_provided|Gorlin_syndrome": 1,
    "not_specified|not_provided|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder|not_provided": 1,
    "Microform_holoprosencephaly|Gorlin_syndrome|not_provided": 1,
    "Gorlin_syndrome|not_specified|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|not_provided": 1,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "not_provided|PTCH1-related_disorder|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7": 1,
    "not_provided|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|not_provided|Gorlin_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Holoprosencephaly_7|Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "PTCH1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_specified": 1,
    "not_provided|Gorlin_syndrome|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Gorlin_syndrome|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Craniopharyngioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|PTCH1-related_disorder|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "Holoprosencephaly_7|Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|not_provided|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|PTCH1-related_disorder": 1,
    "Gorlin_syndrome|not_provided|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome|Craniopharyngioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|not_provided|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "Basal_cell_nevus_syndrome_1|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_adenocarcinoma|Gorlin_syndrome|not_provided|not_specified": 1,
    "Basal_cell_nevus_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Neuroblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|not_specified|not_provided|PTCH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|PTCH1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|PTCH1-related_disorder": 1,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Basal_cell_nevus_syndrome_1|Holoprosencephaly_7": 5,
    "Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7|not_provided": 1,
    "not_provided|PTCH1-related_disorder": 2,
    "Gorlin_syndrome|Basal_cell_carcinoma|_susceptibility_to|_1|Holoprosencephaly_7|not_specified|not_provided|PTCH1-related_disorder": 1,
    "Uterine_leiomyoma|Hereditary_leiomyomatosis_and_renal_cell_cancer": 1,
    "Basal_cell_nevus_syndrome_1|Holoprosencephaly_7|Basal_cell_carcinoma|_susceptibility_to|_1": 1,
    "PTCH1-related_disorder|Basal_cell_carcinoma|_susceptibility_to|_1|Gorlin_syndrome|Holoprosencephaly_7": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Holoprosencephaly_7|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|Pancytopenia-developmental_delay_syndrome": 9,
    "not_provided|ERCC6L2-related_disorder": 8,
    "not_provided|not_specified|ERCC6L2-related_disorder|Pancytopenia-developmental_delay_syndrome": 1,
    "Pancytopenia-developmental_delay_syndrome|not_provided|ERCC6L2-related_disorder": 1,
    "ERCC6L2-related_disorder|not_provided|Pancytopenia-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|ERCC6L2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Pancytopenia-developmental_delay_syndrome": 4,
    "ERCC6L2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|ERCC6L2-related_disorder|Inborn_genetic_diseases|Pancytopenia-developmental_delay_syndrome|not_specified": 1,
    "Pancytopenia-developmental_delay_syndrome|not_provided": 8,
    "ERCC6L2-related_disorder": 6,
    "not_provided|not_specified|Hereditary_cancer|Inborn_genetic_diseases": 1,
    "ERCC6L2-related_disorder|not_provided": 6,
    "Pancytopenia-developmental_delay_syndrome": 16,
    "Inborn_genetic_diseases|not_specified|Pancytopenia-developmental_delay_syndrome|not_provided": 1,
    "not_provided|ERCC6L2-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ERCC6L2-related_disorder|not_provided": 1,
    "ERCC6L2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|ERCC6L2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ERCC6L2-related_disorder|Pancytopenia-developmental_delay_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancytopenia-developmental_delay_syndrome|not_provided": 1,
    "Pancytopenia|Bone_marrow_hypocellularity": 1,
    "not_provided|Premature_ovarian_insufficiency": 3,
    "Pancytopenia-developmental_delay_syndrome|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 1,
    "Bone_marrow_hypocellularity": 2,
    "not_provided|ERCC6L2-related_disorder|Pancytopenia-developmental_delay_syndrome|not_specified": 1,
    "not_specified|not_provided|ERCC6L2-related_disorder|Pancytopenia-developmental_delay_syndrome": 1,
    "not_provided|ERCC6L2-related_disorder|not_specified": 1,
    "not_provided|ERCC6L2-related_disorder|Pancytopenia-developmental_delay_syndrome": 1,
    "Pancytopenia-developmental_delay_syndrome|not_provided|not_specified": 1,
    "not_specified|not_provided|ERCC6L2-related_disorder": 2,
    "ERCC6L2-related_disorder|not_provided|not_specified": 1,
    "Testosterone_17-beta-dehydrogenase_deficiency": 29,
    "HSD17B3-related_disorder": 2,
    "Testosterone_17-beta-dehydrogenase_deficiency|not_provided": 10,
    "Testosterone_17-beta-dehydrogenase_deficiency|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Testosterone_17-beta-dehydrogenase_deficiency|Pseudohermaphroditism": 1,
    "not_provided|Testosterone_17-beta-dehydrogenase_deficiency": 17,
    "HSD17B3-related_disorder|not_provided": 2,
    "Testosterone_17-beta-dehydrogenase_deficiency|Pseudohermaphroditism|not_provided": 1,
    "not_provided|Pseudohermaphroditism|Testosterone_17-beta-dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "Pseudohermaphroditism|not_provided": 2,
    "not_specified|Pseudohermaphroditism": 1,
    "not_provided|HSD17B3-related_disorder|Testosterone_17-beta-dehydrogenase_deficiency": 2,
    "Testosterone_17-beta-dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|HSD17B3-related_disorder": 1,
    "Testosterone_17-beta-dehydrogenase_deficiency|not_provided|Pseudohermaphroditism|Inborn_genetic_diseases": 1,
    "Pseudohermaphroditism|Inborn_genetic_diseases|HSD17B3-related_disorder|not_provided|Testosterone_17-beta-dehydrogenase_deficiency": 1,
    "Pseudohermaphroditism|Testosterone_17-beta-dehydrogenase_deficiency|not_provided": 1,
    "Pseudohermaphroditism|not_provided|Testosterone_17-beta-dehydrogenase_deficiency": 1,
    "not_specified|Testosterone_17-beta-dehydrogenase_deficiency": 1,
    "Sex_development_disorder": 1,
    "See_cases|not_provided|HSD17B3-related_disorder|Testosterone_17-beta-dehydrogenase_deficiency": 1,
    "Testosterone_17-beta-dehydrogenase_deficiency|not_specified|not_provided": 1,
    "not_provided|Mycotic_Aneurysm|_Intracranial": 2,
    "Cataract_36": 79,
    "Cataract_36|not_provided": 7,
    "not_provided|Cataract_36|not_specified": 4,
    "Inborn_genetic_diseases|Cataract_36": 10,
    "not_provided|Cataract_36": 3,
    "TDRD7-related_disorder|Inborn_genetic_diseases": 1,
    "TDRD7-related_disorder|not_provided|Cataract_36": 2,
    "not_specified|not_provided|Cataract_36": 1,
    "Cataract_36|TDRD7-related_disorder": 3,
    "Cataract_36|Inborn_genetic_diseases": 3,
    "Cataract_36|not_specified": 2,
    "Cataract_36|not_provided|not_specified": 1,
    "not_specified|Cataract_36": 1,
    "Cataract_36|Inborn_genetic_diseases|not_provided": 1,
    "TDRD7-related_disorder|Cataract_36": 1,
    "Cataract_36|TDRD7-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cataract_36": 1,
    "not_provided|Xeroderma_pigmentosum_group_A": 14,
    "Xeroderma_pigmentosum_group_A|not_provided": 16,
    "not_specified|Xeroderma_pigmentosum_group_A": 2,
    "Xeroderma_pigmentosum_group_A|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum_group_A|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_A": 5,
    "Xeroderma_pigmentosum_group_A|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum_group_A": 1,
    "not_provided|Xeroderma_pigmentosum_group_A|Xeroderma_pigmentosum": 2,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum_group_A": 1,
    "Xeroderma_pigmentosum_group_A|not_provided|Xeroderma_pigmentosum|not_specified": 1,
    "Xeroderma_pigmentosum_group_A|Xeroderma_pigmentosum|not_provided": 2,
    "Xeroderma_pigmentosum_group_A|not_provided|Xeroderma_pigmentosum": 4,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_A": 5,
    "Xeroderma_pigmentosum_group_A|not_specified|not_provided": 2,
    "Xeroderma_pigmentosum_group_A|XPA-related_disorder|not_provided|Xeroderma_pigmentosum|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum_group_A|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum_group_A|XPA-related_disorder": 1,
    "XPA-related_disorder|not_specified|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|XPA-related_disorder": 2,
    "not_provided|Xeroderma_pigmentosum_group_A|XPA-related_disorder": 1,
    "XPA-related_disorder|not_provided": 1,
    "Bamforth-Lazarus_syndrome": 9,
    "Bamforth-Lazarus_syndrome|not_specified|not_provided": 2,
    "congenital_hypothyreodism": 2,
    "Thyroid_cancer|_nonmedullary|_4": 1,
    "Inborn_genetic_diseases|Bamforth-Lazarus_syndrome": 1,
    "not_specified|Bamforth-Lazarus_syndrome|not_provided": 1,
    "not_specified|FOXE1-related_disorder": 1,
    "FOXE1-related_disorder": 4,
    "not_specified|not_provided|Bamforth-Lazarus_syndrome": 1,
    "Bamforth-Lazarus_syndrome|Thyroid_cancer|_nonmedullary|_4|not_specified|not_provided": 1,
    "Bamforth-Lazarus_syndrome|not_specified": 1,
    "Bamforth-Lazarus_syndrome|Thyroid_cancer|_nonmedullary|_4": 1,
    "Inborn_genetic_diseases|FOXE1-related_disorder": 1,
    "Thyroid_cancer|_nonmedullary|_4|Bamforth-Lazarus_syndrome|not_specified|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_Genevieve_type|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Spondyloepimetaphyseal_dysplasia|_Genevieve_type": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Genevieve_type": 3,
    "not_provided|NANS-related_disorder": 6,
    "Spondyloepimetaphyseal_dysplasia|_Genevieve_type": 12,
    "not_specified|Spondyloepimetaphyseal_dysplasia|_Genevieve_type|not_provided": 1,
    "NANS-related_disorder|not_provided": 1,
    "NANS-related_disorder": 1,
    "not_specified|Myoepithelial_tumor": 1,
    "Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59": 3,
    "not_provided|GABBR2-related_disorder": 2,
    "GABBR2-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_59|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_59|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Epileptic_encephalopathy": 11,
    "not_provided|Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_59": 1,
    "Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills": 6,
    "GABBR2-related_disorder|Epileptic_encephalopathy": 4,
    "Epileptic_encephalopathy|GABBR2-related_disorder": 4,
    "Epileptic_encephalopathy|Inborn_genetic_diseases": 11,
    "Developmental_and_epileptic_encephalopathy|_59": 13,
    "GABBR2-related_disorder|not_provided|Epileptic_encephalopathy": 1,
    "not_provided|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59|Epileptic_encephalopathy": 1,
    "Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59|Tobacco_addiction|_susceptibility_to|Epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_59": 2,
    "not_provided|GABBR2-related_disorder|Epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_59|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills": 1,
    "not_provided|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_59|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Epileptic_encephalopathy": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_59|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills": 1,
    "GABBR2-related_disorder|Epileptic_encephalopathy|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Epileptic_encephalopathy": 7,
    "not_specified|Epileptic_encephalopathy|not_provided": 5,
    "not_provided|Epileptic_encephalopathy|GABBR2-related_disorder": 3,
    "not_specified|Epileptic_encephalopathy": 197,
    "GABBR2-related_disorder|not_provided": 1,
    "GABBR2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_59|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Inborn_genetic_diseases|Rett_syndrome|Epileptic_encephalopathy": 1,
    "not_provided|Epileptic_encephalopathy|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59": 1,
    "Inborn_genetic_diseases|Epileptic_encephalopathy|not_provided": 1,
    "not_specified|Epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 1,
    "Epileptic_encephalopathy|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59": 2,
    "Developmental_and_epileptic_encephalopathy|_59|Tobacco_addiction|_susceptibility_to|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|not_provided|Epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|Developmental_and_epileptic_encephalopathy|_59|Tobacco_addiction|_susceptibility_to": 1,
    "Inborn_genetic_diseases|not_provided|Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_59": 1,
    "Developmental_and_epileptic_encephalopathy|_59|Inborn_genetic_diseases|not_provided|Epileptic_encephalopathy": 1,
    "Neurodevelopmental_disorder_with_poor_language_and_loss_of_hand_skills|not_specified": 1,
    "not_specified|Nephronophthisis_16": 7,
    "Nephronophthisis_16": 288,
    "Nephronophthisis_16|not_provided": 20,
    "Inborn_genetic_diseases|Nephronophthisis_16": 20,
    "Nephronophthisis_16|not_provided|ANKS6-related_disorder": 2,
    "not_provided|Nephronophthisis_16": 13,
    "Nephronophthisis_16|Inborn_genetic_diseases": 22,
    "ANKS6-related_disorder": 7,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis_16": 4,
    "Nephronophthisis_16|ANKS6-related_disorder": 4,
    "Nephronophthisis_16|not_specified|not_provided": 3,
    "Nephronophthisis_16|ANKS6-related_disorder|Inborn_genetic_diseases": 1,
    "ANKS6-related_disorder|Nephronophthisis_16": 1,
    "not_specified|not_provided|Nephronophthisis_16": 4,
    "Nephronophthisis_16|Inborn_genetic_diseases|not_provided": 1,
    "Nephronophthisis_16|not_provided|not_specified": 2,
    "not_provided|Nephronophthisis_16|not_specified": 3,
    "not_provided|ANKS6-related_disorder|Nephronophthisis_16": 2,
    "Inborn_genetic_diseases|Nephronophthisis_16|not_provided": 2,
    "Nephronophthisis_16|not_specified": 2,
    "Nephronophthisis_16|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Nephronophthisis_16": 1,
    "Inborn_genetic_diseases|not_provided|ANKS6-related_disorder|Nephronophthisis_16": 1,
    "ANKS6-related_disorder|Inborn_genetic_diseases|Nephronophthisis_16": 1,
    "Inborn_genetic_diseases|ANKS6-related_disorder|Nephronophthisis_16|not_provided": 1,
    "ANKS6-related_disorder|not_provided|Nephronophthisis_16": 3,
    "not_provided|ANKS6-related_disorder|Nephronophthisis_16|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ANKS6-related_disorder|Nephronophthisis_16": 1,
    "Colorectal_cancer|_susceptibility_to|_1": 40,
    "GALNT12-related_disorder": 3,
    "not_provided|Colorectal_cancer|_susceptibility_to|_1|not_specified": 35,
    "not_provided|Colorectal_cancer|_susceptibility_to|_1": 6,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_1": 28,
    "GALNT12-related_disorder|Colorectal_cancer|_susceptibility_to|_1|not_specified|not_provided": 2,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_1": 10,
    "GALNT12-related_disorder|not_provided|not_specified": 4,
    "not_specified|Colorectal_cancer|_susceptibility_to|_1|not_provided": 17,
    "Colorectal_cancer|_susceptibility_to|_1|not_provided|not_specified": 18,
    "GALNT12-related_disorder|not_specified": 2,
    "Colorectal_cancer|_susceptibility_to|_1|not_specified": 30,
    "Colorectal_cancer|_susceptibility_to|_1|not_specified|not_provided": 42,
    "not_specified|Colorectal_cancer|_susceptibility_to|_1": 18,
    "GALNT12-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_1|not_specified": 3,
    "GALNT12-related_disorder|not_specified|Colorectal_cancer|_susceptibility_to|_1|not_provided": 2,
    "not_specified|not_provided|GALNT12-related_disorder": 5,
    "Colorectal_cancer|_susceptibility_to|_1|not_provided": 5,
    "not_specified|GALNT12-related_disorder|not_provided": 4,
    "not_specified|not_provided|GALNT12-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_1": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_1|not_specified|not_provided": 1,
    "not_specified|Familial_colorectal_cancer|not_provided|Colorectal_cancer|_susceptibility_to|_1|GALNT12-related_disorder": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_1|not_provided|GALNT12-related_disorder": 2,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_1|Breast_neoplasm|GALNT12-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_1|GALNT12-related_disorder|not_specified|not_provided": 1,
    "GALNT12-related_disorder|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_1": 1,
    "GALNT12-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_1|not_specified": 1,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_1|Adenomatous_polyposis_coli|_attenuated|GALNT12-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_1|not_provided|not_specified": 1,
    "GALNT12-related_disorder|not_specified|not_provided": 1,
    "GALNT12-related_disorder|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_1|Colorectal_cancer|not_specified|not_provided": 1,
    "not_specified|not_provided|GALNT12-related_disorder|Colorectal_cancer|_susceptibility_to|_1": 1,
    "COL15A1-related_disorder": 49,
    "not_provided|COL15A1-related_disorder": 3,
    "COL15A1-related_disorder|not_provided": 3,
    "COL15A1-related_disorder|not_specified": 1,
    "Loeys-Dietz_syndrome_1": 64,
    "Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 34,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Multiple_self-healing_squamous_epithelioma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 1,
    "TGFBR1-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1": 1,
    "TGFBR1-related_disorder|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 2,
    "not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|TGFBR1-related_disorder": 1,
    "Thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Loeys-Dietz_syndrome_1|not_provided|Loeys-Dietz_syndrome|Ehlers-Danlos_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR1-related_disorder": 1,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_1": 1,
    "Isolated_thoracic_aortic_aneurysm|not_provided|Loeys-Dietz_syndrome|Multiple_self-healing_squamous_epithelioma|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1": 1,
    "Multiple_self-healing_squamous_epithelioma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma": 1,
    "not_provided|Loeys-Dietz_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 1,
    "TGFBR1-related_disorder|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR1-related_disorder|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 12,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Craniosynostosis_syndrome": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome": 5,
    "Loeys-Dietz_syndrome_1|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFBR1-related_disorder": 4,
    "Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 1,
    "not_provided|Loeys-Dietz_syndrome_1": 4,
    "not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_provided": 4,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Multiple_self-healing_squamous_epithelioma": 1,
    "Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma|not_provided|TGFBR1-related_disorder|not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_1|not_specified|not_provided|TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Loeys-Dietz_syndrome_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|not_provided": 1,
    "Isolated_thoracic_aortic_aneurysm|Loeys-Dietz_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 5,
    "Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "TGFBR1-related_disorder": 1,
    "Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 2,
    "not_provided|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 4,
    "Marfan_syndrome|Loeys-Dietz_syndrome_1|Cardiovascular_phenotype|Multiple_self-healing_squamous_epithelioma|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Multiple_self-healing_squamous_epithelioma": 4,
    "not_provided|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_1": 1,
    "Multiple_self-healing_squamous_epithelioma|not_provided|not_specified": 1,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome": 1,
    "not_provided|not_specified|TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|not_provided|TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 13,
    "TGFBR1-related_disorder|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1661,
    "Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_specified": 1,
    "TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 4,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy|not_provided|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Disproportionate_tall_stature|not_provided": 1,
    "Loeys-Dietz_syndrome|TGFBR1-related_disorder": 1,
    "not_provided|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 1,
    "not_provided|TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFBR1-related_disorder|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome|not_provided|not_specified|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma": 1,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|not_provided|Multiple_self-healing_squamous_epithelioma": 1,
    "Loeys-Dietz_syndrome_1|not_provided": 2,
    "Aortic_aneurysm": 5,
    "Abnormal_palate_morphology|Proportionate_tall_stature|Abnormal_aortic_morphology|Pectus_excavatum|Long_fingers": 1,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_provided|not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|See_cases": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multiple_self-healing_squamous_epithelioma": 1,
    "Loeys-Dietz_syndrome|not_provided": 1,
    "not_provided|Multiple_self-healing_squamous_epithelioma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|not_specified": 1,
    "TGFBR1-related_disorder|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|Multiple_self-healing_squamous_epithelioma": 1,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_provided|TGFBR1-related_disorder|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|See_cases": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 41,
    "TGFBR1-related_disorder|Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "Multiple_self-healing_squamous_epithelioma|Loeys-Dietz_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "TGFBR1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_provided|Loeys-Dietz_syndrome_1": 1,
    "Loeys-Dietz_syndrome_1|Cardiovascular_phenotype": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome_1|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 23,
    "Loeys-Dietz_syndrome_1|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome": 8,
    "not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome|Loeys-Dietz_syndrome_1": 1,
    "Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome": 2,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Loeys-Dietz_syndrome_1": 1,
    "Loeys-Dietz_syndrome|not_provided|Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_1|not_provided|Loeys-Dietz_syndrome": 1,
    "Loeys-Dietz_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|not_provided": 1,
    "not_provided|Loeys-Dietz_syndrome_1|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 143,
    "Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation": 74,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|Inborn_genetic_diseases": 10,
    "ALG2-related_disorder|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 1,
    "Congenital_myasthenic_syndrome_14": 3,
    "Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation": 5,
    "ALG2-related_disorder": 3,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|Inborn_genetic_diseases|not_provided": 2,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_specified|not_provided": 4,
    "ALG2-congenital_disorder_of_glycosylation": 10,
    "not_specified|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|Inborn_genetic_diseases": 1,
    "not_provided|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 3,
    "not_specified|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 11,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_provided": 4,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|ALG2-related_disorder": 1,
    "not_specified|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 2,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_specified": 3,
    "ALG2-related_disorder|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation": 1,
    "Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|See_cases|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|ALG2-related_disorder": 1,
    "not_provided|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation": 1,
    "not_specified|ALG2-related_disorder|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 1,
    "not_provided|not_specified|ALG2-related_disorder|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14": 1,
    "not_provided|See_cases|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_14|not_provided": 1,
    "not_specified|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|ALG2-related_disorder": 2,
    "ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_provided|not_specified": 3,
    "not_specified|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_provided": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation": 1,
    "not_provided|Congenital_myasthenic_syndrome_14|ALG2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "ALG2-related_disorder|ALG2-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_14|not_specified|not_provided": 1,
    "Extraskeletal_myxoid_chondrosarcoma": 2,
    "Infantile_nephronophthisis": 92,
    "Infantile_nephronophthisis|not_provided|Nephronophthisis|Kidney_disorder|not_specified": 1,
    "Infantile_nephronophthisis|not_provided": 5,
    "Infantile_nephronophthisis|Nephronophthisis|not_provided": 1,
    "INVS-related_disorder|Nephronophthisis": 10,
    "Nephronophthisis|Infantile_nephronophthisis": 46,
    "Infantile_nephronophthisis|Nephronophthisis": 35,
    "Nephronophthisis|not_provided|INVS-related_disorder": 3,
    "Nephronophthisis|not_provided|Infantile_nephronophthisis|INVS-related_disorder": 1,
    "Nephronophthisis|INVS-related_disorder": 5,
    "INVS-related_disorder": 16,
    "not_provided|Nephronophthisis|Infantile_nephronophthisis": 3,
    "Nephronophthisis|Inborn_genetic_diseases|Infantile_nephronophthisis": 3,
    "Inborn_genetic_diseases|Nephronophthisis|not_specified|Infantile_nephronophthisis": 1,
    "not_provided|Infantile_nephronophthisis|Nephronophthisis": 5,
    "INVS-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Infantile_nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_nephronophthisis": 1,
    "not_provided|INVS-related_disorder|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Infantile_nephronophthisis|not_provided": 2,
    "Infantile_nephronophthisis|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Infantile_nephronophthisis": 1,
    "not_provided|Infantile_nephronophthisis|Inborn_genetic_diseases|Nephronophthisis": 1,
    "not_provided|Infantile_nephronophthisis|Nephronophthisis|not_specified": 1,
    "Nephronophthisis|not_provided|INVS-related_disorder|Infantile_nephronophthisis": 2,
    "Nephronophthisis|not_provided|not_specified|Infantile_nephronophthisis": 1,
    "INVS-related_disorder|Nephronophthisis|not_specified|not_provided|Infantile_nephronophthisis": 1,
    "Infantile_nephronophthisis|not_specified": 1,
    "Nephronophthisis|not_provided|Infantile_nephronophthisis": 4,
    "Infantile_nephronophthisis|INVS-related_disorder|Inborn_genetic_diseases": 1,
    "Infantile_nephronophthisis|not_provided|not_specified|Nephronophthisis": 1,
    "INVS-related_disorder|Nephronophthisis|not_provided": 1,
    "Nephronophthisis|INVS-related_disorder|not_provided": 3,
    "Nephronophthisis|Infantile_nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Infantile_nephronophthisis": 6,
    "Infantile_nephronophthisis|INVS-related_disorder|Nephronophthisis": 2,
    "INVS-related_disorder|Infantile_nephronophthisis": 1,
    "not_specified|Infantile_nephronophthisis|not_provided|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Infantile_nephronophthisis|INVS-related_disorder": 1,
    "not_provided|Kidney_disorder|not_specified|Nephronophthisis": 1,
    "Nephronophthisis|Infantile_nephronophthisis|Inborn_genetic_diseases": 2,
    "Nephronophthisis|not_specified|INVS-related_disorder|Infantile_nephronophthisis": 1,
    "INVS-related_disorder|not_provided|Nephronophthisis|Infantile_nephronophthisis": 1,
    "Infantile_nephronophthisis|not_specified|Nephronophthisis": 1,
    "Infantile_nephronophthisis|Nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "Infantile_nephronophthisis|INVS-related_disorder|not_provided": 1,
    "Nephronophthisis|INVS-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Infantile_nephronophthisis|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Nephronophthisis|Infantile_nephronophthisis": 1,
    "not_provided|Infantile_nephronophthisis": 2,
    "Nephronophthisis|Infantile_nephronophthisis|INVS-related_disorder": 1,
    "Infantile_nephronophthisis|Kidney_disorder|Nephronophthisis|not_specified": 1,
    "Nephronophthisis|INVS-related_disorder|Inborn_genetic_diseases|Infantile_nephronophthisis": 1,
    "Infantile_nephronophthisis|not_provided|Nephronophthisis|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephronophthisis|INVS-related_disorder": 1,
    "not_provided|INVS-related_disorder|Infantile_nephronophthisis|Nephronophthisis": 2,
    "Infantile_nephronophthisis|Nephronophthisis|not_provided|INVS-related_disorder": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|not_provided|Infantile_nephronophthisis": 1,
    "not_provided|Infantile_nephronophthisis|INVS-related_disorder|Nephronophthisis": 1,
    "Infantile_nephronophthisis|Nephronophthisis|Inborn_genetic_diseases": 4,
    "Nephronophthisis|Infantile_nephronophthisis|not_specified": 1,
    "INVS-related_disorder|Nephronophthisis|not_provided|Infantile_nephronophthisis": 2,
    "Infantile_nephronophthisis|not_specified|not_provided|Nephronophthisis": 2,
    "Infantile_nephronophthisis|Nephronophthisis|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_nephronophthisis|Nephronophthisis": 1,
    "Nephronophthisis|Kidney_failure|not_provided|Infantile_nephronophthisis": 1,
    "INVS-related_disorder|Infantile_nephronophthisis|Nephronophthisis|not_provided|Inborn_genetic_diseases": 1,
    "INVS-related_disorder|Inborn_genetic_diseases|Nephronophthisis|not_provided|not_specified": 1,
    "not_provided|Nephronophthisis|INVS-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Infantile_nephronophthisis": 1,
    "Infantile_nephronophthisis|Inborn_genetic_diseases|Nephronophthisis": 1,
    "Infantile_nephronophthisis|not_provided|Inborn_genetic_diseases|Nephronophthisis|INVS-related_disorder": 1,
    "Kidney_disorder|not_specified|Nephronophthisis|not_provided|Infantile_nephronophthisis": 1,
    "not_provided|Infantile_nephronophthisis|not_specified|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Infantile_nephronophthisis": 1,
    "Inborn_genetic_diseases|Infantile_nephronophthisis|not_provided|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Infantile_nephronophthisis|Nephronophthisis|not_provided": 1,
    "INVS-related_disorder|Infantile_nephronophthisis|Inborn_genetic_diseases|not_provided|Nephronophthisis": 1,
    "Infantile_nephronophthisis|INVS-related_disorder|Nephronophthisis|not_provided": 1,
    "Inborn_genetic_diseases|Infantile_nephronophthisis|Nephronophthisis": 1,
    "INVS-related_disorder|Nephronophthisis|Infantile_nephronophthisis": 1,
    "Inborn_genetic_diseases|Infantile_nephronophthisis|Nephronophthisis|INVS-related_disorder": 1,
    "Infantile_nephronophthisis|Nephronophthisis|INVS-related_disorder": 1,
    "Retinal_dystrophy|Nephronophthisis|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|not_provided|Infantile_nephronophthisis": 1,
    "Nephronophthisis|not_specified|not_provided|Infantile_nephronophthisis": 1,
    "Nephronophthisis|Kidney_failure|not_provided": 1,
    "not_specified|not_provided|Infantile_nephronophthisis|Nephronophthisis": 1,
    "Kidney_disorder|Nephronophthisis|not_specified|Infantile_nephronophthisis": 1,
    "Nephronophthisis|INVS-related_disorder|Infantile_nephronophthisis": 1,
    "INVS-related_disorder|not_specified|not_provided|Nephronophthisis|Infantile_nephronophthisis": 1,
    "not_specified|not_provided|CAVIN4-related_disorder": 1,
    "CAVIN4-related_disorder": 4,
    "not_provided|CAVIN4-related_disorder": 2,
    "CAVIN4-related_disorder|not_specified|not_provided": 1,
    "not_specified|CAVIN4-related_disorder|not_provided": 1,
    "not_provided|Hypercholanemia|_familial_1": 3,
    "Hypercholanemia|_familial": 6,
    "Hypercholanemia|_familial_1|not_provided|Bile_acid_conjugation_defect_1": 1,
    "BAAT-related_disorder|not_provided": 2,
    "Bile_acid_conjugation_defect_1": 6,
    "not_provided|BAAT-related_disorder": 7,
    "BAAT-related_disorder|not_specified|Hypercholanemia|_familial_1|not_provided": 1,
    "not_specified|not_provided|Hypercholanemia|_familial_1": 1,
    "Hypercholanemia|_familial_1|not_specified|not_provided": 2,
    "Bile_acid_conjugation_defect_1|not_provided": 1,
    "Hypercholanemia|_familial|not_specified|not_provided": 1,
    "Hypercholanemia|_familial_1|Bile_acid_conjugation_defect_1|not_provided": 1,
    "BAAT-related_disorder": 10,
    "not_specified|Bile_acid_conjugation_defect_1|not_provided|BAAT-related_disorder": 1,
    "not_provided|Hypercholanemia|_familial_1|not_specified": 1,
    "BAAT-related_disorder|not_specified|not_provided": 1,
    "BAAT-related_disorder|not_provided|not_specified|Hypercholanemia|_familial_1": 1,
    "Hypercholanemia|_familial_1|not_specified": 1,
    "not_specified|BAAT-related_disorder": 2,
    "Hypercholanemia|_familial_1|not_provided|not_specified": 1,
    "not_specified|BAAT-related_disorder|not_provided": 1,
    "not_provided|Hypercholanemia|_familial_1|BAAT-related_disorder": 1,
    "not_specified|not_provided|BAAT-related_disorder": 1,
    "Hypercholanemia|_familial_1|BAAT-related_disorder": 1,
    "not_specified|Hypercholanemia|_familial_1": 1,
    "not_specified|Hypercholanemia|_familial_1|Bile_acid_conjugation_defect_1|not_provided": 1,
    "not_provided|Bile_acid_conjugation_defect_1": 1,
    "not_provided|Hereditary_fructosuria": 22,
    "Hereditary_fructosuria": 404,
    "ALDOB-related_disorder": 8,
    "Hereditary_fructosuria|not_provided": 13,
    "Hereditary_fructosuria|ALDOB-related_disorder": 7,
    "Hereditary_fructosuria|not_specified": 5,
    "ALDOB-related_disorder|not_provided|Hereditary_fructosuria": 2,
    "ALDOB-related_disorder|Hereditary_fructosuria|not_provided": 3,
    "not_specified|ALDOB-related_disorder|Hereditary_fructosuria": 2,
    "ALDOB-related_disorder|not_specified|Inborn_genetic_diseases|Hereditary_fructosuria|not_provided": 1,
    "Hereditary_fructosuria|Inborn_genetic_diseases": 5,
    "not_provided|Hereditary_fructosuria|not_specified": 1,
    "ALDOB-related_disorder|not_provided": 1,
    "ALDOB-related_disorder|Hereditary_fructosuria": 4,
    "not_provided|Hereditary_fructosuria|ALDOB-related_disorder|not_specified": 1,
    "Hereditary_fructosuria|ALDOB-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Hereditary_fructosuria": 2,
    "not_specified|not_provided|Hereditary_fructosuria": 1,
    "Hereditary_fructosuria|not_provided|ALDOB-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_fructosuria|ALDOB-related_disorder|not_provided|See_cases": 1,
    "not_specified|Hereditary_fructosuria": 3,
    "Inborn_genetic_diseases|ALDOB-related_disorder|Hereditary_fructosuria": 1,
    "not_provided|not_specified|Hereditary_fructosuria": 1,
    "ALDOB-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_fructosuria|See_cases": 2,
    "ALDOB-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_fructosuria": 1,
    "ALDOB-related_disorder|Inborn_genetic_diseases|Hereditary_fructosuria": 1,
    "Hereditary_fructosuria|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_fructosuria|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Hereditary_fructosuria|ALDOB-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|ALDOB-related_disorder": 1,
    "not_provided|Hereditary_fructosuria|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_fructosuria|not_provided": 2,
    "Hereditary_fructosuria|ALDOB-related_disorder|not_provided|not_specified": 1,
    "Wiedemann-Rautenstrauch-like_progeroid_syndrome": 3,
    "Familial_High_Density_Lipoprotein_Deficiency|Tangier_disease": 7,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 83,
    "Hypoalphalipoproteinemia|_primary|_1|not_provided|Tangier_disease": 6,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 50,
    "not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 3,
    "not_provided|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 11,
    "Tangier_disease|not_provided|Familial_High_Density_Lipoprotein_Deficiency": 1,
    "Tangier_disease|not_provided|Hypoalphalipoproteinemia|_primary|_1": 3,
    "Tangier_disease|Familial_High_Density_Lipoprotein_Deficiency": 2,
    "Familial_High_Density_Lipoprotein_Deficiency|not_specified|Tangier_disease": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_1|not_specified|Tangier_disease": 6,
    "Tangier_disease|not_specified|not_provided|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Tangier_disease|not_provided": 4,
    "not_provided|Hypoalphalipoproteinemia|_primary|_1|not_specified|Tangier_disease": 2,
    "Tangier_disease": 15,
    "not_provided|ABCA1-related_disorder": 5,
    "ABCA1-related_disorder": 1,
    "Hypoalphalipoproteinemia|_primary|_1|not_specified|Tangier_disease": 1,
    "Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 8,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_provided": 2,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype": 1,
    "Hypoalphalipoproteinemia|_primary|_1": 9,
    "not_specified|not_provided|Tangier_disease": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 2,
    "Cardiovascular_phenotype|High_myopia": 1,
    "not_provided|not_specified|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 2,
    "not_provided|ABCA1-related_disorder|Cardiovascular_phenotype": 2,
    "ABCA1-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_1|not_provided|Tangier_disease|Cardiovascular_phenotype": 2,
    "ABCA1-related_dyslipidemia": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_provided": 5,
    "Familial_hypoalphalipoproteinemia|Decreased_HDL_cholesterol_concentration|Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|ABCA1-related_disorder|not_provided": 1,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_specified|Familial_High_Density_Lipoprotein_Deficiency|not_provided": 1,
    "not_provided|Familial_High_Density_Lipoprotein_Deficiency|not_specified|Tangier_disease": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 4,
    "Tangier_disease|Hypercholesterolemia|_familial|_1": 1,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_specified": 1,
    "Tangier_disease|_variant": 1,
    "Tangier_disease|not_provided|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype": 1,
    "not_specified|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 1,
    "Tangier_disease|ABCA1-related_disorder": 1,
    "not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype": 2,
    "ABCA1-related_disorder|not_provided": 1,
    "not_provided|Neurofibromatosis|_type_1": 333,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided": 2,
    "not_specified|not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 2,
    "not_specified|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 4,
    "not_provided|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype": 3,
    "Hypoalphalipoproteinemia|_primary|_1|not_provided": 2,
    "ABCA1-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|ABCA1-related_disorder|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 1,
    "ABCA1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|ABCA1-related_disorder|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_provided": 5,
    "Cardiovascular_phenotype|ABCA1-related_disorder|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_provided": 1,
    "Cardiovascular_phenotype|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Tangier_disease|Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_specified|not_provided": 1,
    "Tangier_disease|Cardiovascular_phenotype|ABCA1-related_disorder|Hypoalphalipoproteinemia|_primary|_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 1,
    "ABCA1-related_disorder|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Tangier_disease|Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|not_provided": 3,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|not_specified|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype|not_provided": 1,
    "ABCA1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Hypoalphalipoproteinemia|_primary|_1|not_specified|Tangier_disease|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|ABCA1-related_disorder": 1,
    "not_provided|Breast_carcinoma|Reduced_delayed_hypersensitivity|Symphalangism_affecting_the_proximal_phalanx_of_the_4th_finger": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|ABCA1-related_disorder|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 1,
    "Cardiovascular_phenotype|not_specified|Hypoalphalipoproteinemia|_primary|_1|not_provided|Tangier_disease": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_specified|not_provided": 1,
    "not_specified|not_provided|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 1,
    "ABCA1-related_disorder|Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|not_provided|Tangier_disease": 1,
    "Cardiovascular_phenotype|ABCA1-related_disorder|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Familial_High_Density_Lipoprotein_Deficiency|not_specified|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|not_provided|not_specified": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype|not_provided|ABCA1-related_disorder": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype": 1,
    "not_provided|.|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Tangier_disease|Cardiovascular_phenotype|not_provided|ABCA1-related_disorder|not_specified": 1,
    "not_provided|Tangier_disease|Hypoalphalipoproteinemia|_primary|_1|ABCA1-related_disorder": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype|Tangier_disease": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|ABCA1-related_disorder": 1,
    "not_specified|Hypoalphalipoproteinemia|_primary|_1|ABCA1-related_disorder|Cardiovascular_phenotype|not_provided|Tangier_disease": 1,
    "not_specified|Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|not_provided|Tangier_disease": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_1|Tangier_disease": 1,
    "Hypoalphalipoproteinemia|_primary|_1|not_provided|not_specified|Tangier_disease": 1,
    "not_provided|Familial_High_Density_Lipoprotein_Deficiency|Tangier_disease": 2,
    "Familial_High_Density_Lipoprotein_Deficiency|Tangier_disease|not_provided": 1,
    "SLC44A1-related_disorder": 9,
    "Neurodegeneration|_childhood-onset|_with_ataxia|_tremor|_optic_atrophy|_and_cognitive_decline": 3,
    "not_provided|SLC44A1-related_disorder": 1,
    "SLC44A1-related_disorder|not_provided": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 19,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 12,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X": 6,
    "Dilated_cardiomyopathy_1X|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 8,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 45,
    "not_specified|Dilated_cardiomyopathy_1X|FKTN-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_specified|Dilated_Cardiomyopathy|_Recessive": 1,
    "Dilated_cardiomyopathy_1X": 25,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X": 1,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 7,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 9,
    "Walker-Warburg_congenital_muscular_dystrophy": 876,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 117,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided": 31,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 13,
    "Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 8,
    "not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 13,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 64,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_specified": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy": 32,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 2,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy": 8,
    "not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 9,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|FKTN-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|FKTN-related_disorder|Dilated_cardiomyopathy_1X|not_provided|Myopathy_caused_by_variation_in_FKTN|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy": 7,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 1,
    "FKTN-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Hypertrophic_cardiomyopathy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "not_provided|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Dilated_cardiomyopathy_1X": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 2,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|FKTN-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Myopathy_caused_by_variation_in_FKTN|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided": 2,
    "Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|FKTN-related_disorder": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 1,
    "Dilated_cardiomyopathy_1X|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|not_specified": 9,
    "FKTN-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 2,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 2,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 17,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Dilated_Cardiomyopathy|_Recessive|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_specified": 5,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_provided": 1,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 3,
    "FKTN-related_disorder": 1,
    "not_provided|FKTN-related_disorder": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|FKTN-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|FKTN-related_disorder|Dilated_cardiomyopathy_1X|not_specified|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_provided|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Cardiovascular_phenotype": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Cardiovascular_phenotype|not_provided": 1,
    "FKTN-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_provided|Dilated_cardiomyopathy_1X": 1,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|FKTN-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 3,
    "Cardiovascular_phenotype|not_specified|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "FKTN-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Myopathy_caused_by_variation_in_FKTN": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_specified|Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|FKTN-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 2,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X": 1,
    "Cardiovascular_phenotype|FKTN-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|FKTN-related_disorder": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Dilated_cardiomyopathy_1X|not_provided": 1,
    "not_provided|FKTN-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1X": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_specified|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_1X|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|not_provided|FKTN-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M": 3,
    "FKTN-related_disorder|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "FKTN-related_disorder|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Primary_familial_dilated_cardiomyopathy|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1X": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Cardiomyopathy|Ventricular_tachycardia|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 1,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|not_specified|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "FKTN-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1X|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Dilated_Cardiomyopathy|_Recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_Cardiomyopathy|_Recessive": 2,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X": 5,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|not_provided": 5,
    "Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Dilated_cardiomyopathy_1X|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4|Dilated_cardiomyopathy_1X": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Dilated_cardiomyopathy_1X|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2M|Muscular_dystrophy-dystroglycanopathy_(congenital_without_intellectual_disability)|_type_B4": 2,
    "Dilated_Cardiomyopathy|_Recessive|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "not_provided|not_specified|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4|not_provided|Dilated_cardiomyopathy_1X": 1,
    "not_specified|Dilated_cardiomyopathy_1X|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Dilated_Cardiomyopathy|_Recessive|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Osteogenesis_imperfecta_type_14": 4,
    "not_specified|Osteogenesis_imperfecta_type_14|Osteogenesis_imperfecta|not_provided": 1,
    "TMEM38B-related_disorder|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_14": 1,
    "Osteogenesis_imperfecta_type_14|not_provided": 3,
    "Osteogenesis_imperfecta_type_14|TMEM38B-related_disorder": 1,
    "Osteogenesis_imperfecta_type_14|not_provided|Osteogenesis_imperfecta": 1,
    "TMEM38B-related_disorder": 2,
    "Osteogenesis_imperfecta|not_specified|not_provided|TMEM38B-related_disorder": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta": 6,
    "TMEM38B-related_disorder|Osteogenesis_imperfecta_type_14|Inborn_genetic_diseases|not_provided": 1,
    "TMEM38B-related_disorder|not_provided|not_specified": 1,
    "Weiss-Kruszka_syndrome": 91,
    "ZNF462-related_disorder": 37,
    "ZNF462-related_disorder|not_provided": 13,
    "not_provided|Weiss-Kruszka_syndrome": 3,
    "Weiss-Kruszka_syndrome|not_provided": 2,
    "Weiss-Kruszka_syndrome|not_provided|ZNF462-related_disorder": 3,
    "ZNF462-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "ZNF462-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|ZNF462-related_disorder": 6,
    "Weiss-Kruszka_syndrome|Inborn_genetic_diseases": 1,
    "Weiss-Kruszka_syndrome|not_provided|Intellectual_disability|_autosomal_dominant|Craniosynostosis_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Weiss-Kruszka_syndrome": 1,
    "Inborn_genetic_diseases|Weiss-Kruszka_syndrome": 2,
    "Cleft_lip|not_provided": 1,
    "not_provided|ZNF462-related_disorder": 4,
    "Weiss-Kruszka_syndrome|Intellectual_disability|_autosomal_dominant|Craniosynostosis_syndrome": 1,
    "ZNF462-related_disorder|Weiss-Kruszka_syndrome": 2,
    "Intellectual_disability|_autosomal_dominant|Craniosynostosis_syndrome": 1,
    "Weiss-Kruszka_syndrome|not_specified": 1,
    "Weiss-Kruszka_syndrome|ZNF462-related_disorder|Inborn_genetic_diseases": 1,
    "Weiss-Kruszka_syndrome|ZNF462-related_disorder": 1,
    "not_provided|ZNF462-related_disorder|Weiss-Kruszka_syndrome": 1,
    "RAD23B-related_disorder": 3,
    "not_specified|RAD23B-related_disorder": 2,
    "RAD23B-related_disorder|not_provided": 1,
    "not_provided|KLF4-related_disorder": 3,
    "KLF4-related_disorder": 8,
    "KLF4-related_disorder|not_provided": 4,
    "Spermatogenic_failure_86": 6,
    "Male_infertility_with_normal_semen_parameters": 1,
    "Familial_dysautonomia": 363,
    "Familial_dysautonomia|not_provided": 84,
    "not_provided|Familial_dysautonomia": 137,
    "Familial_dysautonomia|Medulloblastoma": 6,
    "not_provided|Familial_dysautonomia|Medulloblastoma|not_specified": 9,
    "Familial_dysautonomia|not_specified|not_provided": 21,
    "not_provided|Medulloblastoma|Familial_dysautonomia": 17,
    "not_specified|Familial_dysautonomia|Medulloblastoma|not_provided": 8,
    "not_specified|Familial_dysautonomia|Medulloblastoma": 8,
    "not_provided|Medulloblastoma|Familial_dysautonomia|not_specified": 5,
    "Familial_dysautonomia|Medulloblastoma|not_provided|not_specified": 13,
    "Medulloblastoma|not_provided|Familial_dysautonomia": 1,
    "not_provided|not_specified|Familial_dysautonomia": 18,
    "ELP1-related_disorder|not_provided|Familial_dysautonomia": 3,
    "Medulloblastoma|Familial_dysautonomia|not_provided": 32,
    "not_specified|not_provided|Familial_dysautonomia": 25,
    "not_provided|Familial_dysautonomia|Medulloblastoma": 27,
    "not_specified|not_provided|Familial_dysautonomia|Medulloblastoma": 15,
    "Medulloblastoma|Familial_dysautonomia": 93,
    "Medulloblastoma|Familial_dysautonomia|not_specified|not_provided": 20,
    "not_specified|Familial_dysautonomia": 4,
    "Medulloblastoma|Familial_dysautonomia|not_provided|not_specified": 9,
    "Familial_dysautonomia|not_provided|not_specified": 11,
    "Familial_dysautonomia|Medulloblastoma|not_provided": 28,
    "not_provided|Familial_dysautonomia|not_specified": 11,
    "ELP1-related_disorder|Medulloblastoma|Familial_dysautonomia|not_provided": 1,
    "not_provided|not_specified|Medulloblastoma|Familial_dysautonomia": 2,
    "not_specified|not_provided|Medulloblastoma|Familial_dysautonomia": 2,
    "ELP1-related_disorder|not_specified|Familial_dysautonomia|not_provided": 1,
    "Familial_dysautonomia|Medulloblastoma|not_specified|not_provided": 15,
    "Familial_dysautonomia|Medulloblastoma|ELP1-related_disorder|not_specified|not_provided": 2,
    "not_specified|Familial_dysautonomia|not_provided": 12,
    "Familial_dysautonomia|not_provided|Medulloblastoma|not_specified": 3,
    "not_specified|not_provided|ELP1-related_disorder|Familial_dysautonomia": 1,
    "Primary_dysautonomia": 1,
    "not_provided|not_specified|Familial_dysautonomia|Medulloblastoma": 5,
    "not_specified|Medulloblastoma|Familial_dysautonomia": 1,
    "not_specified|Medulloblastoma|Familial_dysautonomia|not_provided": 4,
    "Familial_dysautonomia|Medulloblastoma|not_specified": 4,
    "not_specified|ELP1-related_disorder|not_provided": 1,
    "Familial_dysautonomia|Charcot-Marie-Tooth_disease": 1,
    "ELP1-related_disorder|not_provided|Familial_dysautonomia|not_specified": 1,
    "ELP1-related_disorder|not_provided|not_specified|Familial_dysautonomia": 1,
    "Medulloblastoma|not_provided|not_specified": 1,
    "Familial_dysautonomia|not_specified|Medulloblastoma|not_provided": 1,
    "Familial_dysautonomia|not_specified|not_provided|Medulloblastoma": 2,
    "Medulloblastoma|Familial_dysautonomia|Primary_dysautonomia|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "Medulloblastoma|Familial_dysautonomia|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Familial_dysautonomia|ELP1-related_disorder": 1,
    "Familial_dysautonomia|not_provided|Medulloblastoma": 3,
    "not_specified|not_provided|Hereditary_sensory_and_autonomic_neuropathy|Familial_dysautonomia": 1,
    "Medulloblastoma|Familial_dysautonomia|not_specified": 1,
    "Medulloblastoma|Familial_dysautonomia|ELP1-related_disorder|not_specified|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy|not_provided|Familial_dysautonomia|not_specified": 1,
    "ELP1-related_disorder|not_specified|not_provided|Familial_dysautonomia": 1,
    "not_provided|not_specified|Familial_dysautonomia|ELP1-related_disorder": 1,
    "not_provided|Medulloblastoma|ELP1-related_disorder": 1,
    "not_specified|Medulloblastoma": 1,
    "ELP1-related_disorder|Hereditary_sensory_and_autonomic_neuropathy|not_provided|Familial_dysautonomia": 1,
    "Familial_dysautonomia|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_37": 284,
    "Developmental_and_epileptic_encephalopathy|_37|Inborn_genetic_diseases": 15,
    "Seizure|Chorea|Progressive_encephalopathy|Developmental_and_epileptic_encephalopathy|_37": 1,
    "Developmental_and_epileptic_encephalopathy|_37|not_provided": 20,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_37": 12,
    "FRRS1L-related_disorder|Developmental_and_epileptic_encephalopathy|_37": 1,
    "Developmental_and_epileptic_encephalopathy|_37|Seizure|Chorea|Progressive_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_37|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_37|See_cases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_37": 11,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_37|not_provided": 2,
    "not_provided|Seizure|Chorea|Progressive_encephalopathy|FRRS1L-related_disorder|Developmental_and_epileptic_encephalopathy|_37|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_37|Inborn_genetic_diseases": 3,
    "Developmental_and_epileptic_encephalopathy|_37|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_37": 3,
    "Chorea|Progressive_encephalopathy|Seizure|Developmental_and_epileptic_encephalopathy|_37": 1,
    "not_provided|FRRS1L-related_disorder|Developmental_and_epileptic_encephalopathy|_37": 1,
    "FRRS1L-related_disorder|Developmental_and_epileptic_encephalopathy|_37|not_provided": 2,
    "FRRS1L-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_37": 1,
    "Congenital_myasthenic_syndrome_9|not_provided": 2,
    "Congenital_myasthenic_syndrome_9": 15,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided": 21,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 4,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 130,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 393,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided|MUSK-related_disorder": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|not_provided": 8,
    "not_provided|Congenital_myasthenic_syndrome_4C|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 1,
    "Congenital_myasthenic_syndrome_9|MUSK-related_disorder|Fetal_akinesia_deformation_sequence_1": 2,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|MUSK-related_disorder": 2,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 14,
    "not_specified|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided": 4,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|not_specified": 2,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_specified|not_provided": 7,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided": 4,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided|not_specified": 3,
    "Congenital_Myasthenic_Syndrome|_Recessive|MUSK-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 1,
    "not_specified|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 2,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_specified": 7,
    "Congenital_myasthenic_syndrome_9|not_provided|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 2,
    "Congenital_myasthenic_syndrome_4C|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|MUSK-related_disorder|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome_9|not_provided|Fetal_akinesia_deformation_sequence_1": 5,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 10,
    "MUSK-related_disorder|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_specified": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_9|MUSK-related_disorder|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Congenital_myasthenic_syndrome_9|MUSK-related_disorder|Fetal_akinesia_deformation_sequence_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 1,
    "MUSK-related_disorder|not_specified|not_provided": 1,
    "MUSK-related_disorder": 4,
    "MUSK-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|not_specified|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|not_specified|not_provided": 2,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 4,
    "not_provided|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 8,
    "not_provided|Fetal_akinesia_deformation_sequence_1": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 3,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|not_provided": 6,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Congenital_myasthenic_syndrome_9": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 1,
    "Congenital_myasthenic_syndrome_9|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1": 1,
    "MUSK-related_disorder|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 2,
    "Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 1,
    "MUSK-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|not_provided": 1,
    "Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided|Delayed_gross_motor_development|Bilateral_ptosis|Respiratory_insufficiency|Stridor": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9|MUSK-related_disorder": 1,
    "Inborn_genetic_diseases|MUSK-related_disorder|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_Myasthenic_Syndrome|_Recessive|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_9": 1,
    "not_specified|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_9": 1,
    "Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|not_provided|Delayed_gross_motor_development|Bilateral_ptosis|Stridor|Respiratory_insufficiency": 1,
    "MUSK-related_disorder|Congenital_myasthenic_syndrome_9|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Spermatogenic_failure_75": 7,
    "Spermatogenic_failure_75|SHOC1-related_condition": 1,
    "not_provided|Congenital_nonbullous_ichthyosiform_erythroderma": 1,
    "INIP-related_disorder": 1,
    "Neurodegeneration_and_seizures_due_to_copper_transport_defect|not_provided": 1,
    "Neurodegeneration_and_seizures_due_to_copper_transport_defect": 1,
    "Retinitis_pigmentosa_70|not_specified|not_provided": 1,
    "not_provided|PRPF4-related_disorder": 5,
    "PRPF4-related_disorder": 1,
    "PRPF4-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_70|not_provided": 1,
    "Retinitis_pigmentosa_70": 2,
    "Retinitis_pigmentosa_70|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_70|not_provided|not_specified": 1,
    "Porphobilinogen_synthase_deficiency|not_provided": 20,
    "Porphobilinogen_synthase_deficiency": 66,
    "not_provided|Porphobilinogen_synthase_deficiency": 7,
    "Porphobilinogen_synthase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Porphobilinogen_synthase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Porphobilinogen_synthase_deficiency": 2,
    "ALAD-related_disorder": 2,
    "Porphobilinogen_synthase_deficiency|Inborn_genetic_diseases": 1,
    "Porphobilinogen_synthase_deficiency|ALAD-related_disorder|not_provided": 1,
    "not_provided|Porphobilinogen_synthase_deficiency|ALAD*1/ALAD*2_POLYMORPHISM|not_specified": 1,
    "not_specified|Porphobilinogen_synthase_deficiency|not_provided": 1,
    "not_provided|PORPHYRIA|_ACUTE_HEPATIC|_DIGENIC": 1,
    "not_provided|ALAD-related_disorder": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_8|not_provided": 2,
    "KIF12-related_disorder": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_8": 9,
    "Inborn_genetic_diseases|KIF12-related_disorder|not_provided": 1,
    "KIF12-related_disorder|not_provided": 1,
    "Steel_syndrome|not_provided": 36,
    "Steel_syndrome": 32,
    "not_provided|Steel_syndrome": 20,
    "COL27A1-related_disorder|not_provided": 13,
    "Inborn_genetic_diseases|not_provided|COL27A1-related_disorder": 2,
    "Inborn_genetic_diseases|COL27A1-related_disorder|not_provided": 1,
    "COL27A1-related_disorder": 4,
    "not_provided|COL27A1-related_disorder": 14,
    "not_provided|COL27A1-related_disorder|Steel_syndrome": 2,
    "not_provided|COL27A1-related_disorder|Inborn_genetic_diseases": 1,
    "COL27A1-related_disorder|Steel_syndrome|not_provided": 1,
    "Steel_syndrome|not_provided|COL27A1-related_disorder": 1,
    "Steel_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Steel_syndrome": 1,
    "Steel_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Steel_syndrome|not_provided": 1,
    "AKNA-related_autism_spectrum_disorder": 1,
    "Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 13,
    "Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 33,
    "not_provided|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 6,
    "Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive": 6,
    "Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_provided": 5,
    "Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided": 14,
    "Usher_syndrome_type_2D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31": 3,
    "not_provided|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_specified": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 15,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|WHRN-related_disorder|not_provided": 1,
    "Usher_syndrome_type_2D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Retinal_dystrophy|not_specified": 1,
    "not_specified|not_provided|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 7,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 1,
    "Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|Optic_atrophy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_31": 4,
    "not_provided|Usher_syndrome_type_2D|Retinitis_pigmentosa-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_provided|WHRN-related_disorder": 1,
    "WHRN-related_disorder|not_provided": 7,
    "not_provided|Retinal_dystrophy|not_specified|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "not_provided|Usher_syndrome_type_2D|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31": 3,
    "Usher_syndrome|not_provided|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 6,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided": 1,
    "WHRN-related_disorder|not_specified|not_provided": 3,
    "Usher_syndrome_type_2D": 4,
    "Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|WHRN-related_disorder": 1,
    "WHRN-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|Hearing_impairment": 1,
    "WHRN-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 1,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_specified": 1,
    "Usher_syndrome_type_2D|WHRN-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided|not_specified": 1,
    "not_specified|not_provided|Aland_island_eye_disease|Retinal_dystrophy": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_specified": 3,
    "not_provided|not_specified|Usher_syndrome_type_2D|Retinitis_pigmentosa-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "WHRN-related_disorder|not_provided|not_specified": 2,
    "WHRN-related_disorder|Retinal_dystrophy|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 1,
    "Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided|not_specified": 2,
    "WHRN-related_disorder|not_specified|not_provided|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_specified|not_provided": 2,
    "WHRN-related_disorder": 2,
    "not_provided|not_specified|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 2,
    "not_provided|not_specified|Retinitis_pigmentosa-deafness_syndrome|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 1,
    "not_specified|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|Hearing_impairment": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided|WHRN-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|WHRN-related_disorder": 1,
    "not_provided|Usher_syndrome_type_2D": 2,
    "not_provided|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 1,
    "not_specified|Usher_syndrome_type_2D|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided|WHRN-related_disorder": 1,
    "Usher_syndrome_type_2D|not_provided": 1,
    "Usher_syndrome_type_2D|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_31|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D|not_provided|not_specified": 1,
    "not_specified|not_provided|Retinitis_pigmentosa-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_31|Usher_syndrome_type_2D": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_31": 1,
    "Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "TNC-related_disorder": 31,
    "TNC-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_56": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_56": 23,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56": 22,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56|not_specified": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56|not_provided": 17,
    "not_provided|TNC-related_disorder": 10,
    "not_specified|TNC-related_disorder|not_provided": 3,
    "TNC-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_56": 3,
    "not_specified|TNC-related_disorder": 3,
    "TNC-related_disorder|not_specified": 3,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_56": 4,
    "not_provided|TNC-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_56": 1,
    "TNC-related_disorder|not_provided": 2,
    "not_provided|not_specified|TNC-related_disorder": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_56": 1,
    "Meniere_disease|not_provided|TNC-related_disorder": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_56|not_specified|TNC-related_disorder": 1,
    "TNC-related_disorder|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56|TNC-related_disorder|not_provided": 2,
    "TNC-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_56|not_provided": 3,
    "not_provided|TNC-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56|TNC-related_disorder|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56|Progressive_sensorineural_hearing_impairment|Myopia|Vertigo": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_56|not_specified|not_provided|TNC-related_disorder": 1,
    "TNC-related_disorder|Meniere_disease": 1,
    "not_specified|TNC-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_56|not_provided": 1,
    "ASTN2-related_disorder": 26,
    "ASTN2-related_disorder|not_provided|not_specified": 1,
    "ASTN2-related_disorder|not_provided": 4,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 11,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided": 6,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 46,
    "TRIM32-related_disorder": 21,
    "TRIM32-related_disorder|not_provided": 2,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome": 21,
    "Bardet-Biedl_syndrome|not_provided|TRIM32-related_disorder": 6,
    "Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 5,
    "not_provided|TRIM32-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "Bardet-Biedl_syndrome|TRIM32-related_disorder|not_provided": 2,
    "Bardet-Biedl_syndrome|Sarcotubular_myopathy|TRIM32-related_disorder|Bardet-Biedl_syndrome_11": 1,
    "Bardet-Biedl_syndrome|TRIM32-related_disorder": 15,
    "Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome": 4,
    "not_provided|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 4,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|not_specified|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome": 7,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "not_provided|TRIM32-related_disorder": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome|not_provided": 3,
    "TRIM32-related_disorder|not_provided|Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 11,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome": 1,
    "not_provided|not_specified|TRIM32-related_disorder|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "not_provided|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|TRIM32-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 5,
    "not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome": 3,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome": 4,
    "TRIM32-related_disorder|not_provided|Bardet-Biedl_syndrome": 3,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|not_specified|TRIM32-related_disorder": 3,
    "TRIM32-related_disorder|not_provided|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|TRIM32-related_disorder": 2,
    "not_provided|TRIM32-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|not_provided": 1,
    "TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome": 4,
    "TRIM32-related_disorder|not_provided|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|TRIM32-related_disorder": 1,
    "Bardet-Biedl_syndrome|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "not_provided|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome|Autosomal_recessive_limb-girdle_muscular_dystrophy|TRIM32-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "TRIM32-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Bardet-Biedl_syndrome|not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|TRIM32-related_disorder": 3,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 3,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 3,
    "Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|TRIM32-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|TRIM32-related_disorder|Bardet-Biedl_syndrome|not_provided": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome|not_provided|not_specified": 1,
    "TRIM32-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|Bardet-Biedl_syndrome": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|not_provided": 2,
    "TRIM32-related_disorder|not_specified|not_provided|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome|TRIM32-related_disorder": 2,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|not_provided|TRIM32-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Limb-girdle_muscular_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "Bardet-Biedl_syndrome|not_provided|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_specified": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome|Inborn_genetic_diseases|TRIM32-related_disorder": 1,
    "Bardet-Biedl_syndrome_11": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome|TRIM32-related_disorder": 1,
    "not_provided|Sarcotubular_myopathy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11": 1,
    "not_provided|Bardet-Biedl_syndrome|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome|not_provided": 2,
    "not_provided|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|Bardet-Biedl_syndrome|TRIM32-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|Inborn_genetic_diseases|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 2,
    "TRIM32-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|TRIM32-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 4,
    "not_specified|not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome": 1,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome": 2,
    "not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|Bardet-Biedl_syndrome": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|TRIM32-related_disorder": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_specified|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|TRIM32-related_disorder|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided": 1,
    "TRIM32-related_disorder|not_provided|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Bardet-Biedl_syndrome|not_provided|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|TRIM32-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome|Sarcotubular_myopathy|TRIM32-related_disorder|Bardet-Biedl_syndrome_11|not_provided": 2,
    "Sarcotubular_myopathy|Inborn_genetic_diseases|Bardet-Biedl_syndrome_11": 1,
    "TRIM32-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Myopathy|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome|not_provided|TRIM32-related_disorder": 1,
    "TRIM32-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_provided": 1,
    "not_provided|Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome|TRIM32-related_disorder": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|Inborn_genetic_diseases|TRIM32-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_specified": 1,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|not_specified|Bardet-Biedl_syndrome|not_provided": 1,
    "Sarcotubular_myopathy|TRIM32-related_disorder|Bardet-Biedl_syndrome_11": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided": 2,
    "Sarcotubular_myopathy|Bardet-Biedl_syndrome_11|TRIM32-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "TRIM32-related_disorder|Sarcotubular_myopathy|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_11|Sarcotubular_myopathy|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Bardet-Biedl_syndrome|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "ASTN2-related_disorder|not_specified": 1,
    "not_provided|ASTN2-related_disorder": 1,
    "TLR4-related_disorder": 5,
    "TLR4-related_disorder|not_provided": 1,
    "not_specified|Susceptibility_to_severe_COVID-19": 1,
    "COPD|_severe_early_onset|Pericementitis|Susceptibility_to_severe_coronavirus_disease_(COVID-19)|TLR4_POLYMORPHISM|not_provided": 1,
    "COPD|_severe_early_onset|TLR4_POLYMORPHISM|not_provided": 1,
    "Microcephaly_3|_primary|_autosomal_recessive": 106,
    "Microcephaly_3|_primary|_autosomal_recessive|not_provided": 30,
    "Microcephaly_3|_primary|_autosomal_recessive|not_specified|not_provided|CDK5RAP2-related_disorder": 3,
    "CDK5RAP2-related_disorder|not_provided": 10,
    "Microcephaly_3|_primary|_autosomal_recessive|not_provided|not_specified": 3,
    "not_provided|Microcephaly_3|_primary|_autosomal_recessive|not_specified": 2,
    "Microcephaly_3|_primary|_autosomal_recessive|not_provided|not_specified|CDK5RAP2-related_disorder|Primary_Microcephaly|_Recessive": 1,
    "not_specified|not_provided|Primary_Microcephaly|_Recessive": 3,
    "Microcephaly_3|_primary|_autosomal_recessive|not_specified": 2,
    "Inborn_genetic_diseases|Microcephaly_3|_primary|_autosomal_recessive": 3,
    "not_provided|Primary_Microcephaly|_Recessive|not_specified": 1,
    "CDK5RAP2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "CDK5RAP2-related_disorder|not_provided|Microcephaly_3|_primary|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|not_provided|Microcephaly_3|_primary|_autosomal_recessive": 5,
    "not_provided|Microcephaly_3|_primary|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "not_provided|Microcephaly_3|_primary|_autosomal_recessive": 12,
    "CDK5RAP2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "CDK5RAP2-related_disorder": 8,
    "not_provided|not_specified|CDK5RAP2-related_disorder|Primary_Microcephaly|_Recessive": 1,
    "not_provided|CDK5RAP2-related_disorder": 6,
    "Primary_Microcephaly|_Recessive|not_specified|not_provided|Microcephaly_3|_primary|_autosomal_recessive": 1,
    "not_specified|Microcephaly_3|_primary|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|Microcephaly_3|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|Primary_Microcephaly|_Recessive|not_specified|Microcephaly_3|_primary|_autosomal_recessive": 1,
    "not_specified|Microcephaly_3|_primary|_autosomal_recessive": 1,
    "Microcephaly_3|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases|CDK5RAP2-related_disorder": 1,
    "CDK5RAP2-related_disorder|not_provided|not_specified": 2,
    "Microcephaly_3|_primary|_autosomal_recessive|CDK5RAP2-related_disorder|not_provided": 1,
    "Primary_Microcephaly|_Recessive|not_specified|not_provided": 4,
    "Microcephaly_3|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CDK5RAP2-related_disorder": 1,
    "not_provided|Microcephaly_3|_primary|_autosomal_recessive|CDK5RAP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Microcephaly_3|_primary|_autosomal_recessive": 3,
    "not_provided|Microcephaly_3|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_specified": 2,
    "not_provided|Microcephaly_3|_primary|_autosomal_recessive|CDK5RAP2-related_disorder": 1,
    "Microcephaly_3|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Primary_Microcephaly|_Recessive|not_specified": 1,
    "Microcephaly_3|_primary|_autosomal_recessive|Inborn_genetic_diseases": 5,
    "CDK5RAP2-related_disorder|not_specified|not_provided": 1,
    "Microcephaly_3|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_specified|not_provided": 1,
    "CDK5RAP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Microcephaly_3|_primary|_autosomal_recessive": 1,
    "not_provided|Hypotonia|Congenital_ocular_coloboma|intellectual_deficiency": 1,
    "not_specified|not_provided|Microcephaly_3|_primary|_autosomal_recessive": 2,
    "Microcephaly_3|_primary|_autosomal_recessive|not_specified|not_provided": 3,
    "not_provided|not_specified|Primary_Microcephaly|_Recessive": 2,
    "not_provided|Primary_Microcephaly|_Recessive|Microcephaly_3|_primary|_autosomal_recessive|not_specified": 1,
    "not_specified|not_provided|Microcephaly_3|_primary|_autosomal_recessive|CDK5RAP2-related_disorder": 1,
    "Primary_Microcephaly|_Recessive|not_provided|not_specified": 4,
    "not_provided|Inborn_genetic_diseases|Microcephaly_3|_primary|_autosomal_recessive": 1,
    "CDK5RAP2-related_disorder|Microcephaly_3|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|CDK5RAP2-related_disorder|Primary_Microcephaly|_Recessive|not_specified": 1,
    "Inborn_genetic_diseases|CDK5RAP2-related_disorder": 1,
    "Microcephaly_3|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_provided|not_specified": 1,
    "not_provided|Complement_component_5_deficiency|Eculizumab|_poor_response_to": 28,
    "not_provided|Eculizumab|_poor_response_to|Complement_component_5_deficiency|not_specified": 3,
    "not_specified|not_provided|Complement_component_5_deficiency|Eculizumab|_poor_response_to": 3,
    "not_provided|Eculizumab|_poor_response_to|Complement_component_5_deficiency": 7,
    "Complement_component_5_deficiency|Eculizumab|_poor_response_to|not_provided": 20,
    "Complement_component_5_deficiency": 8,
    "not_specified|not_provided|Eculizumab|_poor_response_to|Complement_component_5_deficiency": 3,
    "Eculizumab|_poor_response_to|Complement_component_5_deficiency|not_provided": 19,
    "not_provided|not_specified|Eculizumab|_poor_response_to|Complement_component_5_deficiency": 1,
    "not_specified|C5-related_disorder": 2,
    "Complement_component_5_deficiency|Eculizumab|_poor_response_to": 1,
    "C5-related_disorder|not_provided": 7,
    "not_specified|not_provided|Complement_component_5_deficiency": 1,
    "not_provided|C5-related_disorder": 3,
    "not_specified|Complement_component_5_deficiency|not_provided": 2,
    "not_specified|Complement_component_5_deficiency|Eculizumab|_poor_response_to|not_provided": 1,
    "not_provided|Complement_component_5_deficiency": 2,
    "not_provided|not_specified|C5-related_disorder": 2,
    "C5-related_disorder|Complement_component_5_deficiency|Eculizumab|_poor_response_to|not_provided": 1,
    "not_provided|C5-related_disorder|Complement_component_5_deficiency|Eculizumab|_poor_response_to": 1,
    "Eculizumab|_poor_response_to|not_provided": 1,
    "C5-related_disorder": 3,
    "not_specified|Eculizumab|_poor_response_to|Complement_component_5_deficiency|not_provided": 1,
    "Complement_component_5_deficiency|Eculizumab|_poor_response_to|not_specified|not_provided": 3,
    "Eculizumab|_poor_response_to|Complement_component_5_deficiency|not_specified|not_provided": 2,
    "Complement_component_5_deficiency|Eculizumab|_poor_response_to|not_provided|not_specified": 1,
    "not_provided|not_specified|Complement_component_5_deficiency|Eculizumab|_poor_response_to": 3,
    "C5-related_disorder|not_specified|not_provided|Complement_component_5_deficiency": 1,
    "C5-related_disorder|not_provided|not_specified": 1,
    "not_provided|C5-related_disorder|not_specified": 1,
    "Complement_component_5_deficiency|not_provided|C5-related_disorder": 1,
    "Complement_component_5_deficiency|not_provided": 1,
    "not_provided|Lathosterolosis|C5-related_disorder|Complement_component_5_deficiency|Eculizumab|_poor_response_to": 1,
    "RAB14-related_disorder": 1,
    "GSN-related_disorder": 6,
    "Finnish_type_amyloidosis": 62,
    "not_provided|Inborn_genetic_diseases|Finnish_type_amyloidosis": 9,
    "Finnish_type_amyloidosis|Inborn_genetic_diseases|not_provided": 12,
    "Inborn_genetic_diseases|Finnish_type_amyloidosis|not_provided": 12,
    "not_provided|Finnish_type_amyloidosis|Inborn_genetic_diseases": 12,
    "not_provided|Finnish_type_amyloidosis": 40,
    "Finnish_type_amyloidosis|not_provided": 55,
    "Finnish_type_amyloidosis|not_provided|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Finnish_type_amyloidosis": 8,
    "not_specified|Finnish_type_amyloidosis|not_provided": 2,
    "Finnish_type_amyloidosis|GSN-related_disorder|not_provided": 4,
    "Finnish_type_amyloidosis|not_provided|not_specified": 1,
    "GSN-related_disorder|Inborn_genetic_diseases|Finnish_type_amyloidosis|not_provided": 1,
    "not_provided|Finnish_type_amyloidosis|GSN-related_disorder": 2,
    "not_provided|GSN-related_disorder": 3,
    "not_provided|Finnish_type_amyloidosis|GSN-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Finnish_type_amyloidosis|Inborn_genetic_diseases|not_provided": 3,
    "Finnish_type_amyloidosis|Inborn_genetic_diseases": 2,
    "Finnish_type_amyloidosis|not_provided|GSN-related_disorder": 2,
    "not_provided|GSN-related_disorder|Finnish_type_amyloidosis": 1,
    "Inborn_genetic_diseases|Finnish_type_amyloidosis": 2,
    "not_specified|Inborn_genetic_diseases|Finnish_type_amyloidosis|not_provided": 1,
    "Finnish_type_amyloidosis|not_provided|Amyloidosis": 1,
    "Inborn_genetic_diseases|not_provided|GSN-related_disorder": 1,
    "Inborn_genetic_diseases|Finnish_type_amyloidosis|not_provided|GSN-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Finnish_type_amyloidosis": 1,
    "GSN-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Finnish_type_amyloidosis": 1,
    "GSN-related_disorder|Finnish_type_amyloidosis|not_specified|not_provided": 1,
    "not_provided|Finnish_type_amyloidosis|Inborn_genetic_diseases|not_specified|GSN-related_disorder": 1,
    "Finnish_type_amyloidosis|GSN-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Finnish_type_amyloidosis|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Finnish_type_amyloidosis": 1,
    "Finnish_type_amyloidosis|GSN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Amyloidosis": 8,
    "Amyloidosis|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_37": 4,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_37": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_37|not_specified": 1,
    "PTGS1-related_disorder|not_provided": 1,
    "Hemorrhage|not_specified": 1,
    "PTGS1-related_disorder": 1,
    "Ventriculomegaly-cystic_kidney_disease|not_provided": 11,
    "Inborn_genetic_diseases|not_provided|CRB2-related_disorder": 2,
    "CRB2-related_disorder|Focal_segmental_glomerulosclerosis_9|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_9": 17,
    "CRB2-related_disorder": 28,
    "not_provided|CRB2-related_disorder": 17,
    "CRB2-related_disorder|not_provided": 18,
    "not_specified|not_provided|CRB2-related_disorder": 1,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|not_provided": 4,
    "Focal_segmental_glomerulosclerosis_9|Ventriculomegaly-cystic_kidney_disease|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_9|Ventriculomegaly-cystic_kidney_disease": 3,
    "not_specified|CRB2-related_disorder|not_provided": 1,
    "not_provided|Ventriculomegaly-cystic_kidney_disease": 7,
    "CRB2-related_disorder|Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|not_provided": 1,
    "CRB2-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Ventriculomegaly-cystic_kidney_disease": 3,
    "CRB2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|CRB2-related_disorder": 1,
    "not_provided|Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|Inborn_genetic_diseases": 1,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|not_provided|CRB2-related_disorder": 1,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9": 1,
    "not_provided|CRB2-related_disorder|Inborn_genetic_diseases": 3,
    "Focal_segmental_glomerulosclerosis_9|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|CRB2-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_9|not_provided": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_9": 2,
    "Focal_segmental_glomerulosclerosis_9|not_provided": 1,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|not_specified|not_provided": 1,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9": 1,
    "Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis_9": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|CRB2-related_disorder|Ventriculomegaly-cystic_kidney_disease": 1,
    "CRB2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_9": 2,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|Inborn_genetic_diseases|not_provided": 2,
    "Ventriculomegaly-cystic_kidney_disease|Familial_idiopathic_steroid-resistant_nephrotic_syndrome|not_provided": 1,
    "Ventriculomegaly-cystic_kidney_disease|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|CRB2-related_disorder": 1,
    "Inborn_genetic_diseases|CRB2-related_disorder": 1,
    "not_provided|Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|CRB2-related_disorder": 1,
    "Ventriculomegaly-cystic_kidney_disease|Focal_segmental_glomerulosclerosis_9|Inborn_genetic_diseases|CRB2-related_disorder|not_provided|Steroid-resistant_nephrotic_syndrome": 1,
    "not_provided|Obesity|CRB2-related_disorder|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_9|Immunodeficiency|_common_variable|_7|Inborn_genetic_diseases|CRB2-related_disorder|not_provided": 1,
    "CRB2-related_disorder|not_specified": 1,
    "not_provided|CRB2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_9|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_9|CRB2-related_disorder|not_provided": 1,
    "Variable_neurodevelopmental_disorder": 1,
    "LHX2-related_disorder": 4,
    "LHX2-associated_neurodevelopmental_disorder": 1,
    "not_provided|LHX2-related_disorder": 2,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|not_provided": 2,
    "Male_infertility|not_specified|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 1,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 35,
    "not_provided|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 4,
    "NR5A1-related_disorder": 11,
    "not_provided|NR5A1-related_disorder": 2,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development": 50,
    "46|XY_sex_reversal_3|Oligosynaptic_infertility|46|XY_disorder_of_sex_development": 2,
    "46|XY_sex_reversal_3|Premature_ovarian_failure_7": 1,
    "NR5A1-related_disorder|Oligosynaptic_infertility|46|XY_disorder_of_sex_development|46|XY_sex_reversal_3": 1,
    "Spermatogenic_failure_8|Male_infertility|Non-obstructive_azoospermia": 1,
    "Male_infertility|Premature_ovarian_failure_7|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 1,
    "Male_infertility|Non-obstructive_azoospermia": 1,
    "46|XY_sex_reversal_3|Non-obstructive_azoospermia": 1,
    "NR5A1-related_disorder|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 1,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|Genetic_non-acquired_premature_ovarian_failure|not_provided": 1,
    "not_provided|46|XY_sex_reversal_3|Oligosynaptic_infertility|46|XY_disorder_of_sex_development|Genetic_non-acquired_premature_ovarian_failure": 1,
    "Premature_ovarian_failure_7|46|XY_sex_reversal_3": 4,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|not_specified|not_provided": 1,
    "46|XY_sex_reversal_3|NR5A1-related_disorder": 1,
    "not_specified|Oligosynaptic_infertility|46|XY_disorder_of_sex_development": 1,
    "NR5A1-related_disorder|not_provided": 1,
    "ADRENAL_INSUFFICIENCY|_NR5A1-RELATED": 1,
    "Inborn_genetic_diseases|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 1,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|46|XY_sex_reversal_3": 1,
    "46|XY_sex_reversal_3|Non-obstructive_azoospermia|not_provided|Oligosynaptic_infertility|46|XY_disorder_of_sex_development|Male_infertility|Spermatogenic_failure_8": 1,
    "NR5A1-related_disorder|46|XY_disorder_of_sex_development|Oligosynaptic_infertility|not_provided": 1,
    "Premature_ovarian_failure_7": 3,
    "46|XX_sex_reversal_4": 1,
    "Spermatogenic_failure_8": 4,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|not_provided|NR5A1-related_disorder": 1,
    "not_provided|Oligosynaptic_infertility|46|XY_disorder_of_sex_development|not_specified": 1,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|not_provided|not_specified": 1,
    "not_provided|46|XY_disorder_of_sex_development|Oligosynaptic_infertility|not_specified": 2,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|Male_infertility|not_provided": 1,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|Inborn_genetic_diseases": 1,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|not_specified": 1,
    "not_specified|not_provided|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 1,
    "not_provided|Oligosynaptic_infertility|46|XY_disorder_of_sex_development": 2,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|NR5A1-related_disorder|not_provided": 1,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|not_provided|NR5A1-related_disorder|not_specified|Spermatogenic_failure_8": 1,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "46|XY_sex_reversal_3|ADRENAL_INSUFFICIENCY|_NR5A1-RELATED|46|XX_sex_reversal_4": 1,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|46|XX_sex_reversal_4|not_provided|46|XY_sex_reversal_3": 1,
    "not_provided|46|XY_sex_reversal_3": 1,
    "46|XY_sex_reversal_3|46|XY_disorder_of_sex_development|Oligosynaptic_infertility|NR5A1-related_disorder": 1,
    "46|XY_sex_reversal_3|NR5A1-related_disorder|Oligosynaptic_infertility|46|XY_disorder_of_sex_development": 1,
    "46|XY_sex_reversal_3|not_provided|Genetic_non-acquired_premature_ovarian_failure": 1,
    "46|XY_sex_reversal_3|Premature_ovarian_failure_7|46|XX_sex_reversal_4|Spermatogenic_failure_8|46|XY_disorder_of_sex_development|Oligosynaptic_infertility": 1,
    "46|XY_sex_reversal_3|Disorder_of_sexual_differentiation": 1,
    "Oligosynaptic_infertility|46|XY_sex_reversal_3": 1,
    "not_specified|Oligosynaptic_infertility|46|XY_disorder_of_sex_development|not_provided": 1,
    "Oligosynaptic_infertility|46|XY_disorder_of_sex_development|Disorder_of_sexual_differentiation": 1,
    "46|XY_sex_reversal_3|Spermatogenic_failure_8|46|XX_sex_reversal_4|Premature_ovarian_failure_7|not_provided": 1,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|not_provided": 1,
    "46|XY_disorder_of_sex_development|Oligosynaptic_infertility|46|XX_sex_reversal_4": 1,
    "OCULOVERTEBRAL_SYNDROME": 2,
    "RPL35-related_disorder": 3,
    "RPL35-related_disorder|not_provided": 3,
    "Diamond-Blackfan_anemia_19": 1,
    "not_provided|RPL35-related_disorder": 2,
    "GAPVD1-related_disorder": 32,
    "not_provided|FAM157B-related_disorder": 1,
    "GAPVD1-related_disorder|not_provided": 2,
    "FAM157B-related_disorder": 1,
    "not_provided|GAPVD1-related_disorder": 1,
    "GAPVD1-related_Nephrotic_syndrome": 1,
    "X-linked_cone-rod_dystrophy": 6,
    "MVB12B-related_disorder": 7,
    "not_provided|MVB12B-related_disorder": 1,
    "Nail-patella_syndrome": 155,
    "Nail-patella_syndrome|not_provided": 34,
    "LMX1B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Nail-patella_syndrome|Nail-patella-like_renal_disease": 20,
    "Inborn_genetic_diseases|Nail-patella_syndrome|Nail-patella-like_renal_disease": 1,
    "not_provided|Nail-patella-like_renal_disease|Nail-patella_syndrome": 2,
    "not_provided|Nail-patella_syndrome|Nail-patella-like_renal_disease|not_specified": 1,
    "LMX1B-related_disorder|not_provided": 6,
    "not_provided|Nail-patella_syndrome|Nail-patella-like_renal_disease": 18,
    "not_provided|Nail-patella_syndrome": 38,
    "Nail-patella_syndrome|Nail-patella-like_renal_disease|LMX1B-related_disorder|not_provided": 1,
    "LMX1B-related_disorder": 11,
    "not_provided|Nail-patella-like_renal_disease": 1,
    "Nail-patella_syndrome|Nail-patella-like_renal_disease|not_provided": 13,
    "not_provided|LMX1B-related_disorder": 4,
    "Inborn_genetic_diseases|Nail-patella_syndrome": 1,
    "Nail-patella-like_renal_disease|Nail-patella_syndrome|not_provided|not_specified": 1,
    "LMX1B-related_disorder|Kidney_disorder|not_provided": 1,
    "Nail-patella-like_renal_disease": 4,
    "not_provided|Focal_segmental_glomerulosclerosis|not_specified|Nail-patella_syndrome|Nail-patella-like_renal_disease": 1,
    "not_provided|not_specified|Nail-patella-like_renal_disease|Nail-patella_syndrome": 1,
    "Nail-patella_syndrome|Nail-patella-like_renal_disease|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Nail-patella_syndrome|Nail-patella-like_renal_disease|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Nail-patella_syndrome|Nail-patella-like_renal_disease": 1,
    "Nail-patella_syndrome|not_provided|Focal_segmental_glomerulosclerosis|Nail-patella-like_renal_disease": 1,
    "Inborn_genetic_diseases|Nail-patella_syndrome|not_provided": 2,
    "LMX1B-related_disorder|Nail-patella_syndrome|Nail-patella-like_renal_disease|not_provided": 1,
    "not_specified|not_provided|Nail-patella-like_renal_disease|Nail-patella_syndrome": 1,
    "Nail-patella-like_renal_disease|Nail-patella_syndrome|Nephrotic_syndrome|not_provided|Inherited_focal_segmental_glomerulosclerosis|LMX1B-related_disorder": 1,
    "Nail-patella-like_renal_disease|Lipoid_nephrosis": 1,
    "Nail-patella_syndrome|LMX1B-related_disorder|not_provided": 1,
    "not_specified|LMX1B-related_disorder|not_provided|Nail-patella_syndrome": 1,
    "not_provided|LMX1B-related_disorder|not_specified": 1,
    "Kidney_disorder|not_provided|Inborn_genetic_diseases": 1,
    "LMX1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Nail-patella_syndrome|Nail-patella-like_renal_disease|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Nail-patella_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "Nail-patella_syndrome|Nail-patella-like_renal_disease|not_provided|LMX1B-related_disorder": 1,
    "Nail-patella-like_renal_disease|Inborn_genetic_diseases|Nail-patella_syndrome|not_provided": 1,
    "not_specified|not_provided|Nail-patella_syndrome": 1,
    "LMX1B-related_disorder|Nail-patella_syndrome|not_provided|Nail-patella-like_renal_disease": 1,
    "Focal_segmental_glomerulosclerosis|Nail-patella_syndrome|Nail-patella-like_renal_disease|not_provided": 1,
    "not_specified|LMX1B-related_disorder|not_provided|Nail-patella_syndrome|Nail-patella-like_renal_disease": 1,
    "Inborn_genetic_diseases|Nail-patella-like_renal_disease|Nail-patella_syndrome|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided": 24,
    "Charcot-Marie-Tooth_disease_axonal_type_2P": 537,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_specified": 5,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases": 40,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 13,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P": 31,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_specified|not_provided": 3,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases": 2,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 17,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2P": 9,
    "LRSAM1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2P": 4,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided|Charcot-Marie-Tooth_disease|not_specified": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P": 19,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|not_provided": 8,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 5,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|LRSAM1-related_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided": 8,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided|Inborn_genetic_diseases": 5,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided|LRSAM1-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|not_provided": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 2,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided|LRSAM1-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|LRSAM1-related_disorder|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2P|LRSAM1-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease|not_specified|not_provided": 2,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P": 3,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|LRSAM1-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P": 2,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|not_specified|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease_axonal_type_2P-AR|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P|LRSAM1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Inborn_genetic_diseases|not_provided|LRSAM1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2P|not_provided": 1,
    "Inborn_genetic_diseases|LRSAM1-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2P": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2P|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2P|Charcot-Marie-Tooth_disease|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_4": 139,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4": 7,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Inborn_genetic_diseases|STXBP1-related_disorder": 1,
    "STXBP1-related_neurodevelopmental_disorder": 1,
    "Infantile_epilepsy_syndrome|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy": 9,
    "Intellectual_disability|Spasticity": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Early_onset_epileptic_encephalopathy|not_specified": 1,
    "not_provided|Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_4|not_provided": 6,
    "Multiple_congenital_anomalies/dysmorphic_syndrome|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|STXBP1-related_disorder|not_specified": 1,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|_4|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_4": 7,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|STXBP1-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_4": 3,
    "STXBP1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Infantile_epilepsy_syndrome|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 2,
    "STXBP1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Infantile_epilepsy_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Spastic_ataxia|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4": 1,
    "STXBP1-related_disorder|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Global_developmental_delay|Atypical_behavior|Seizure|Hand_tremor|Macrocephaly": 1,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Intellectual_disability|Strabismus|Generalized_hypotonia|Axial_hypotonia|Infantile_spasms|Global_developmental_delay|Delayed_speech_and_language_development|Horizontal_nystagmus": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4": 3,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Intellectual_disability|Seizure|See_cases": 1,
    "Spastic_ataxia|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy|not_provided|Autism_spectrum_disorder": 1,
    "not_specified|not_provided|STXBP1-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Neurodevelopmental_delay": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_4|Photosensitive_tonic-clonic_seizure|Neurodegeneration|Autism|Intellectual_disability|_severe|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "See_cases|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Infantile_epilepsy_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Infantile_epilepsy_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Infantile_epilepsy_syndrome|STXBP1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Cerebellar_vermis_hypoplasia|Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4|Inborn_genetic_diseases": 2,
    "STXBP1-related_disorder": 7,
    "Severe_global_developmental_delay|Microcephaly": 1,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4": 2,
    "not_provided|Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Developmental_and_epileptic_encephalopathy|Infantile_epilepsy_syndrome": 2,
    "Developmental_and_epileptic_encephalopathy|_4|Intellectual_disability": 2,
    "Developmental_and_epileptic_encephalopathy|_4|not_provided|Developmental_and_epileptic_encephalopathy": 3,
    "not_provided|Infantile_epilepsy_syndrome": 5,
    "Developmental_and_epileptic_encephalopathy|_4|Neurodevelopmental_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy": 3,
    "Developmental_and_epileptic_encephalopathy|not_specified|STXBP1-related_disorder": 2,
    "STXBP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Infantile_epilepsy_syndrome|West_syndrome|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_4|Early_onset_epileptic_encephalopathy|Spastic_ataxia": 1,
    "Infantile_epilepsy_syndrome|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4": 2,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|STXBP1-related_disorder|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|not_specified|STXBP1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4|not_provided": 1,
    "Cerebellar_vermis_hypoplasia|West_syndrome|Developmental_and_epileptic_encephalopathy|_4|STXBP1-related_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Infantile_epilepsy_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Severe_intellectual_deficiency": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Inborn_genetic_diseases": 1,
    "Cerebellar_ataxia|Moderate_global_developmental_delay|Tremor|Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Intellectual_disability|Epileptic_encephalopathy": 1,
    "Cerebellar_ataxia|Intellectual_disability": 3,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Infantile_epilepsy_syndrome|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Epileptic_encephalopathy": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_4|Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Epileptic_encephalopathy|not_provided": 1,
    "Infantile_epilepsy_syndrome|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|STXBP1-related_disorder": 2,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Intellectual_disability|Epileptic_encephalopathy": 1,
    "Autism|Global_developmental_delay": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_4|not_specified": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Developmental_and_epileptic_encephalopathy|_4|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_4|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Infantile_epilepsy_syndrome|Developmental_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_4|See_cases|Seizure": 1,
    "Seizure|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_4": 1,
    "Infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|_4|STXBP1-associated_neurodevelopmental_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "STXBP1-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "STXBP1-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant": 8,
    "not_provided|CDK9-related_disorder": 1,
    "CDK9-related_disorder": 11,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1": 142,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 8,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1": 3,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Moyamoya_disease_2": 58,
    "ENG-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1": 4,
    "ENG-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia": 2,
    "ENG-related_disorder": 8,
    "Hereditary_hemorrhagic_telangiectasia": 679,
    "Hereditary_hemorrhagic_telangiectasia|not_provided": 18,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|not_specified": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 75,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 5,
    "ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Haemorrhagic_telangiectasia_1|not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 2,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 110,
    "not_provided|Hereditary_hemorrhagic_telangiectasia": 25,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 13,
    "Juvenile_Polyposis|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia": 13,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_specified|Hereditary_hemorrhagic_telangiectasia|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 5,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_specified": 4,
    "Cardiovascular_phenotype|not_provided|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 53,
    "Hereditary_hemorrhagic_telangiectasia|not_specified": 4,
    "ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|ENG-related_disorder": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|not_specified|Hereditary_hemorrhagic_telangiectasia": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Hereditary_hemorrhagic_telangiectasia": 2,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 7,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 3,
    "Hereditary_hemorrhagic_telangiectasia|not_provided|not_specified": 1,
    "not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Pulmonary_arterial_hypertension|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 8,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|not_provided|not_specified": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 30,
    "Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 6,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Pulmonary_hypertension|_primary|_1|Cardiovascular_phenotype|not_specified|not_provided|Hereditary_hemorrhagic_telangiectasia|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|ENG-related_disorder": 1,
    "Cardiovascular_phenotype|ENG-related_disorder|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|not_provided|Cardiovascular_phenotype": 1,
    "Telangiectasia_of_the_skin|Palate_telangiectasia|Spontaneous|_recurrent_epistaxis|Oral_cavity_telangiectasia|Pulmonary_arteriovenous_malformation": 1,
    "Cardiovascular_phenotype|not_provided|Hereditary_hemorrhagic_telangiectasia": 8,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided": 5,
    "Cardiovascular_phenotype|not_specified|Hereditary_hemorrhagic_telangiectasia": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1": 4,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|not_provided": 7,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 6,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype|not_provided": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 3,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Juvenile_Polyposis": 3,
    "not_specified|Hereditary_hemorrhagic_telangiectasia": 8,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided": 3,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1": 3,
    "Hereditary_hemorrhagic_telangiectasia|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 2,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 8,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 3,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|Haemorrhagic_telangiectasia_1": 1,
    "Haemorrhagic_telangiectasia_1|Cardiovascular_phenotype|not_provided|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_specified|not_provided|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_specified|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia": 5,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 3,
    "not_specified|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder|not_provided|Hereditary_hemorrhagic_telangiectasia": 1,
    "ENG-related_disorder|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype|not_provided|Hereditary_hemorrhagic_telangiectasia": 2,
    "Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder": 2,
    "Hereditary_hemorrhagic_telangiectasia|Juvenile_polyposis_syndrome": 1,
    "ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 3,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_specified|Pulmonary_arterial_hypertension|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 2,
    "not_provided|ENG-related_disorder|Cardiovascular_phenotype": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_specified": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|not_specified": 1,
    "not_provided|ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|not_provided": 4,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1": 5,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 1,
    "Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cerebral_arteriovenous_malformation": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|not_specified|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|ENG-related_disorder": 1,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 2,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Systemic_lupus_erythematosus": 1,
    "not_provided|ENG-related_disorder|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 2,
    "not_provided|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder": 2,
    "not_specified|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 1,
    "Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|Pulmonary_hypertension|_primary|_1|Haemorrhagic_telangiectasia_1": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder": 1,
    "ENG-related_disorder|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|not_provided": 1,
    "Cardiovascular_phenotype|ENG-related_disorder|not_provided|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia|not_specified": 1,
    "See_cases|Hereditary_hemorrhagic_telangiectasia|not_provided|ENG-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 1,
    "Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Haemorrhagic_telangiectasia_1|Galloway-Mowat_syndrome_1|not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 1,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Cardiovascular_phenotype": 2,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 2,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Pulmonary_arterial_hypertension": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_specified|ENG-related_disorder": 1,
    "not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_provided|See_cases|Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder|Cardiovascular_phenotype|not_specified|Hereditary_hemorrhagic_telangiectasia": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_specified": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Hereditary_hemorrhagic_telangiectasia|See_cases|not_provided": 1,
    "ENG-related_disorder|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 1,
    "See_cases|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Hereditary_hemorrhagic_telangiectasia|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_specified|not_provided|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|ENG-related_disorder": 1,
    "not_specified|Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided": 1,
    "Hereditary_hemorrhagic_telangiectasia|ENG-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Juvenile_Polyposis": 1,
    "Hemolytic_anemia_due_to_adenylate_kinase_deficiency": 26,
    "Hemolytic_anemia_due_to_adenylate_kinase_deficiency|not_provided": 11,
    "not_provided|Hemolytic_anemia_due_to_adenylate_kinase_deficiency": 5,
    "not_specified|Hemolytic_anemia_due_to_adenylate_kinase_deficiency": 3,
    "Hemolytic_anemia_due_to_adenylate_kinase_deficiency|not_specified": 2,
    "not_specified|Hemolytic_anemia_due_to_adenylate_kinase_deficiency|not_provided": 1,
    "Adenylate_kinase_deficiency|Hemolytic_anemia_due_to_adenylate_kinase_deficiency": 1,
    "AK1-related_condition|Hemolytic_anemia_due_to_adenylate_kinase_deficiency|not_provided": 1,
    "Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy": 95,
    "not_specified|not_provided|Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy": 2,
    "not_provided|not_specified|Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy": 1,
    "not_provided|Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy": 3,
    "not_specified|Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy": 2,
    "Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy|not_provided|not_specified": 1,
    "DPM2-related_disorder|Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy": 1,
    "not_provided|Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy|not_specified|DPM2-related_disorder": 1,
    "Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy|not_specified": 1,
    "Congenital_muscular_dystrophy_with_intellectual_disability_and_severe_epilepsy|not_provided": 2,
    "Nephrolithiasis": 1,
    "Dystonic_disorder|not_specified": 24,
    "not_specified|Dystonic_disorder": 26,
    "not_provided|CIZ1-related_disorder|Dystonic_disorder": 1,
    "Dystonia|_primary_cervical": 1,
    "Dystonia_23": 4,
    "Dystonic_disorder|CIZ1-related_disorder": 3,
    "not_provided|Dystonic_disorder|CIZ1-related_disorder": 2,
    "not_specified|Dystonic_disorder|not_provided": 2,
    "CIZ1-related_disorder|Dystonic_disorder": 2,
    "CIZ1-related_disorder|Dystonic_disorder|not_provided": 1,
    "Dystonic_disorder|not_provided|CIZ1-related_disorder": 1,
    "CIZ1-related_disorder": 1,
    "Variant_of_unknown_significance|Dystonic_disorder": 1,
    "not_provided|CIZ1-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_31A": 25,
    "not_provided|Developmental_and_epileptic_encephalopathy|_31A|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|Inborn_genetic_diseases": 7,
    "Developmental_and_epileptic_encephalopathy|_31B": 4,
    "Developmental_and_epileptic_encephalopathy|_31A|not_provided": 35,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A": 17,
    "not_provided|Cerebellar_ataxia|Global_developmental_delay|Stereotypic_movement_disorder|Epileptic_encephalopathy|Seizure|Hypotonia|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_31A": 11,
    "DNM1-related_disorder": 7,
    "Developmental_and_epileptic_encephalopathy|_31A|not_provided|DNM1-related_disorder": 1,
    "DNM1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A": 2,
    "DNM1-related_disorder|Developmental_and_epileptic_encephalopathy|_31A": 4,
    "Developmental_and_epileptic_encephalopathy|_31A|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_31A|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|not_specified": 15,
    "Developmental_and_epileptic_encephalopathy|_31A|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A": 4,
    "Developmental_and_epileptic_encephalopathy|_31A|not_provided|Inborn_genetic_diseases": 1,
    "Lennox-Gastaut_syndrome|West_syndrome": 1,
    "not_provided|DNM1-related_disorder|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A|not_specified": 4,
    "DNM1-related_disorders": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A|not_provided": 5,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|DNM1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|Inborn_genetic_diseases|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|See_cases": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_31A|DNM1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_31B|Developmental_and_epileptic_encephalopathy": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_31A|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_31A|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|not_specified|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_31A|not_provided|Inborn_genetic_diseases|DNM1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|DNM1-related_disorder": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_31A|DNM1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|Developmental_and_epileptic_encephalopathy|_1|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|Developmental_and_epileptic_encephalopathy|_31B": 1,
    "DNM1-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_31A|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|not_specified|not_provided|DNM1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|DNM1-related_disorder|Developmental_and_epileptic_encephalopathy|_31A|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_31A|not_provided|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_31A|not_provided": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "DNM1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A|not_provided": 1,
    "not_provided|DNM1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_31A": 1,
    "DNM1-related_disorder|Developmental_and_epileptic_encephalopathy|_31A|Inborn_genetic_diseases|not_specified": 1,
    "Developmental_delay_with_hypotonia|_myopathy|_and_brain_abnormalities|Neuromuscular_disease": 1,
    "not_provided|GOLGA2-related_disorder": 1,
    "Developmental_delay_with_hypotonia|_myopathy|_and_brain_abnormalities": 4,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_specified": 4,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Spastic_ataxia_10|_autosomal_recessive": 3,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 190,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Inborn_genetic_diseases": 3,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_provided": 16,
    "not_provided|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Spastic_ataxia_10|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 6,
    "not_provided|not_specified|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 2,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|COQ4-related_disorder": 3,
    "Spastic_ataxia_10|_autosomal_recessive": 4,
    "not_provided|Inborn_genetic_diseases|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 1,
    "not_specified|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 2,
    "COQ4-related_disorder": 1,
    "Inborn_genetic_diseases|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_provided": 2,
    "not_provided|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Inborn_genetic_diseases|Spastic_ataxia_10|_autosomal_recessive": 1,
    "Spastic_ataxia|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 2,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_provided|COQ4-related_disorder": 1,
    "Spastic_ataxia_10|_autosomal_recessive|Spastic_ataxia|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 1,
    "not_provided|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 5,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_specified|not_provided": 1,
    "Spastic_ataxia_10|_autosomal_recessive|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 4,
    "Spastic_ataxia_10|_autosomal_recessive|not_provided|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 1,
    "not_provided|Spastic_ataxia_10|_autosomal_recessive|COQ4-related_disorder|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome": 1,
    "not_provided|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_specified": 1,
    "not_specified|Spastic_ataxia_10|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_provided|Developmental_disorder": 1,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Spastic_ataxia_10|_autosomal_recessive|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 1,
    "Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_provided|not_specified": 1,
    "Spastic_ataxia_10|_autosomal_recessive|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_specified": 1,
    "COQ4-related_disorder|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Inborn_genetic_diseases": 1,
    "COQ4-related_disorder|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|not_provided": 1,
    "COQ4-related_disorder|Spastic_ataxia_10|_autosomal_recessive|Neonatal_encephalomyopathy-cardiomyopathy-respiratory_distress_syndrome|Inborn_genetic_diseases|Spastic_ataxia|not_provided": 1,
    "Ichthyosis_prematurity_syndrome": 19,
    "not_provided|Ichthyosis_prematurity_syndrome": 5,
    "Inborn_genetic_diseases|not_provided|SLC27A4-related_disorder": 1,
    "not_specified|SLC27A4-related_disorder|not_provided": 1,
    "not_provided|SLC27A4-related_disorder": 2,
    "Ichthyosis_prematurity_syndrome|Autosomal_recessive_congenital_ichthyosis|not_provided": 1,
    "Ichthyosis_prematurity_syndrome|not_specified": 2,
    "Lamellar_ichthyosis|not_provided|Ichthyosis_prematurity_syndrome": 1,
    "Ichthyosis_prematurity_syndrome|Inborn_genetic_diseases": 2,
    "Ichthyosis_prematurity_syndrome|not_provided": 3,
    "Ichthyosis_prematurity_syndrome|not_provided|Lamellar_ichthyosis": 1,
    "Ichthyosis_prematurity_syndrome|not_provided|not_specified": 1,
    "Lamellar_ichthyosis|Ichthyosis_prematurity_syndrome|not_provided": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1|not_provided": 6,
    "Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome": 34,
    "not_provided|Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome": 6,
    "Lethal_congenital_contractural_syndrome_Finnish_type": 36,
    "GLE1-related_disorder|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Inborn_genetic_diseases": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome": 8,
    "not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1|Lethal_congenital_contractural_syndrome_Finnish_type": 1,
    "not_provided|GLE1-related_disorder": 2,
    "not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome": 5,
    "Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_provided": 5,
    "Lethal_congenital_contractural_syndrome_Finnish_type|GLE1-related_disorder|not_provided": 1,
    "Lethal_congenital_contractural_syndrome_Finnish_type|not_provided": 11,
    "GLE1-related_disorder": 5,
    "not_provided|Lethal_congenital_contractural_syndrome_Finnish_type": 6,
    "Lethal_congenital_contractural_syndrome_Finnish_type|Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_1|not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contractural_syndrome_Finnish_type": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1": 10,
    "GLE1-related_disorder|Lethal_congenital_contractural_syndrome_Finnish_type|not_provided": 1,
    "Inborn_genetic_diseases|Lethal_congenital_contractural_syndrome_Finnish_type|not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1": 1,
    "Inborn_genetic_diseases|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contractural_syndrome_Finnish_type|Lethal_congenital_contracture_syndrome_1|not_provided": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contractural_syndrome_Finnish_type|Lethal_congenital_contracture_syndrome_1": 1,
    "Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_specified|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_specified|not_provided|Lethal_congenital_contractural_syndrome_Finnish_type": 1,
    "Inborn_genetic_diseases|not_provided|Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome": 1,
    "not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1": 4,
    "not_provided|Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_specified": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contractural_syndrome_Finnish_type|Lethal_congenital_contracture_syndrome_1|not_provided": 1,
    "not_provided|Lethal_congenital_contractural_syndrome_Finnish_type|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contracture_syndrome_1": 1,
    "Lethal_congenital_contracture_syndrome_1|not_specified|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_provided": 1,
    "not_provided|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|GLE1-related_disorder": 1,
    "Lethal_congenital_contracture_syndrome_1": 2,
    "GLE1-related_disorder|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_1|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|Lethal_congenital_contractural_syndrome_Finnish_type|Inborn_genetic_diseases|not_provided": 1,
    "Lethal_congenital_contractural_syndrome_Finnish_type|Inborn_genetic_diseases|not_provided": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_provided|Lethal_congenital_contracture_syndrome_1": 1,
    "Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_provided": 2,
    "Amyotrophic_lateral_sclerosis|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome": 1,
    "Lethal_congenital_contracture_syndrome|Lethal_arthrogryposis-anterior_horn_cell_disease_syndrome|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_5": 70,
    "SPTAN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy": 13,
    "not_specified|SPTAN1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 9,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "SPTAN1-related_disorder": 18,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|not_specified": 5,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 12,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_provided": 7,
    "Developmental_and_epileptic_encephalopathy|_5|not_provided|Developmental_and_epileptic_encephalopathy": 8,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "Neurodevelopmental_abnormality|Developmental_and_epileptic_encephalopathy|_5|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Developmental_delay_with_or_without_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_5": 4,
    "Slurred_speech|Limb_ataxia": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 3,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 5,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 3,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy": 6,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy": 3,
    "SPTAN1-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_delay_with_or_without_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_provided|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_5|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|not_provided": 6,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy": 6,
    "Developmental_delay_with_or_without_epilepsy": 7,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 3,
    "not_specified|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 2,
    "Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 2,
    "SPTAN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 2,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5|Abnormal_brain_morphology": 1,
    "Distal_lower_limb_muscle_weakness": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 15,
    "Distal_spinal_muscular_atrophy|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_5": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 3,
    "not_provided|Inborn_genetic_diseases|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5|Intellectual_disability": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 8,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|SPTAN1-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 3,
    "Developmental_and_epileptic_encephalopathy|_5|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 3,
    "Developmental_and_epileptic_encephalopathy|_5|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Developmental_delay_with_or_without_epilepsy|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Self-limited_epilepsy_with_centrotemporal_spikes|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_provided|Inborn_genetic_diseases|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 4,
    "Neuromuscular_disease|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|SPTAN1-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_5|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_5|not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11": 5,
    "Developmental_and_epileptic_encephalopathy|_5|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_provided": 2,
    "not_provided|Distal_spinal_muscular_atrophy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases|Landau-Kleffner_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_specified|Developmental_and_epileptic_encephalopathy": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 6,
    "Inborn_genetic_diseases|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_specified": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_5|Developmental_delay_with_or_without_epilepsy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_provided|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Self-limited_epilepsy_with_centrotemporal_spikes|not_specified|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases": 2,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_5|Lymphedema": 1,
    "Developmental_and_epileptic_encephalopathy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5|Peripheral_neuropathy": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_provided|SPTAN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|SPTAN1-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_delay_with_or_without_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_delay_with_or_without_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_specified|not_provided": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "SPTAN1-related_disorder|Inborn_genetic_diseases|not_specified|Microcephaly|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_5": 2,
    "SPTAN1-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_specified": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|not_specified": 1,
    "SPTAN1-related_disorder|Congenital_cerebellar_hypoplasia|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|not_specified|SPTAN1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "not_provided|SPTAN1-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_provided|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type": 170,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_5|Neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_5|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Developmental_delay_with_or_without_epilepsy|Developmental_and_epileptic_encephalopathy|_5|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5|Bilateral_tonic-clonic_seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Werdnig-Hoffmann_disease|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|Developmental_and_epileptic_encephalopathy|_5|Spastic_paraplegia_91|_autosomal_dominant|_with_or_without_cerebellar_ataxia|Developmental_delay_with_or_without_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 2,
    "not_specified|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_5": 3,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|SPTAN1-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_11|not_provided": 1,
    "SPTAN1-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|SPTAN1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|not_provided": 1,
    "SPTAN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_5|Undetermined_early-onset_epileptic_encephalopathy": 1,
    "SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5|not_provided|See_cases|Developmental_delay_with_or_without_epilepsy|Developmental_and_epileptic_encephalopathy|Focal_epilepsy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_5|Epileptic_encephalopathy": 1,
    "Developmental_disorder|Intellectual_disability": 2,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Developmental_and_epileptic_encephalopathy|_5|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|_5|not_specified|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5|not_provided": 1,
    "Developmental_delay_with_or_without_epilepsy|not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Inborn_genetic_diseases|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|SPTAN1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|SPTAN1-related_disorder|not_specified": 1,
    "SPTAN1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_5|Lymphedema": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_5|SPTAN1-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_5|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_5|not_specified|Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5|not_provided|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_5|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|SPTAN1-related_disorder|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_5": 1,
    "DYNC2I2-related_disorder": 3,
    "Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 356,
    "Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 33,
    "not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 9,
    "DYNC2I2-related_disorder|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 6,
    "not_specified|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|Retinal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Jeune_thoracic_dystrophy|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 2,
    "Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|DYNC2I2-related_disorder": 5,
    "Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|not_provided": 8,
    "Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|not_provided|DYNC2I2-related_disorder": 2,
    "not_specified|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 1,
    "not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|DYNC2I2-related_disorder": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 2,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 1,
    "not_specified|not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 2,
    "Retinal_dystrophy|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 2,
    "not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|not_specified": 1,
    "DYNC2I2-related_disorder|not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 1,
    "Jeune_thoracic_dystrophy|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 1,
    "not_provided|not_specified|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly": 1,
    "DYNC2I2-related_disorder|not_provided": 1,
    "DYNC2I2-related_disorder|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|See_cases|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Short-rib_thoracic_dysplasia_11_with_or_without_polydactyly|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_58": 2,
    "SET-related_disorder|Global_developmental_delay|Intellectual_disability|_autosomal_dominant_58|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_58|not_provided": 4,
    "not_provided|SET-related_disorder": 1,
    "SET-related_disorder": 6,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_58": 1,
    "Intellectual_disability|_autosomal_dominant_58|Inborn_genetic_diseases": 1,
    "SPOUT1-related_disorder": 11,
    "SPOUT1-associated_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_poor_growth|_seizures|_and_brain_abnormalities|Neurodevelopmental_disorder": 1,
    "SPOUT1_Associated_Development_delay_Microcephaly_Seizures_Short_stature": 2,
    "Neurodevelopmental_disorder_with_poor_growth|_seizures|_and_brain_abnormalities|Neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_poor_growth|_seizures|_and_brain_abnormalities|Neurodevelopmental_disorder|not_specified": 1,
    "Neurodevelopmental_disorder_with_poor_growth|_seizures|_and_brain_abnormalities|Undetermined_early-onset_epileptic_encephalopathy|Neurodevelopmental_disorder": 1,
    "SPOUT1-related_disorder|not_provided": 1,
    "Agammaglobulinemia_5|_autosomal_dominant|LRRC8A-related_disorder": 1,
    "not_provided|Agammaglobulinemia_5|_autosomal_dominant": 4,
    "not_provided|Agammaglobulinemia_5|_autosomal_dominant|LRRC8A-related_disorder": 1,
    "not_provided|LRRC8A-related_disorder": 6,
    "Agammaglobulinemia_5|_autosomal_dominant|not_provided": 1,
    "LRRC8A-related_disorder|not_provided|not_specified": 1,
    "LRRC8A-related_disorder|not_provided": 6,
    "LRRC8A-related_disorder": 1,
    "not_provided|not_specified|Agammaglobulinemia_5|_autosomal_dominant": 2,
    "not_provided|Agammaglobulinemia_5|_autosomal_dominant|not_specified": 1,
    "Agammaglobulinemia_5|_autosomal_dominant|LRRC8A-related_disorder|not_provided": 2,
    "LRRC8A-related_disorder|Agammaglobulinemia_5|_autosomal_dominant|not_specified|not_provided": 1,
    "LRRC8A-related_disorder|Agammaglobulinemia_5|_autosomal_dominant|not_provided": 2,
    "LRRC8A-related_disorder|not_provided|Agammaglobulinemia_5|_autosomal_dominant": 1,
    "Agammaglobulinemia_5|_autosomal_dominant|not_provided|not_specified": 1,
    "Agammaglobulinemia_5|_autosomal_dominant": 1,
    "not_provided|not_specified|LRRC8A-related_disorder": 1,
    "DK1-congenital_disorder_of_glycosylation": 206,
    "Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation": 64,
    "DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype": 63,
    "DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype|DOLK-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|DK1-congenital_disorder_of_glycosylation": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|DK1-congenital_disorder_of_glycosylation": 4,
    "Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|not_provided": 7,
    "not_specified|Cardiovascular_phenotype|not_provided|DK1-congenital_disorder_of_glycosylation": 1,
    "not_specified|DK1-congenital_disorder_of_glycosylation|DOLK-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|DK1-congenital_disorder_of_glycosylation": 11,
    "not_specified|Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation": 3,
    "DK1-congenital_disorder_of_glycosylation|not_provided": 5,
    "not_provided|DK1-congenital_disorder_of_glycosylation": 5,
    "not_specified|DK1-congenital_disorder_of_glycosylation|Hypertrophic_cardiomyopathy_26|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|not_specified": 1,
    "DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype": 2,
    "DOLK-related_disorder|DK1-congenital_disorder_of_glycosylation": 1,
    "DK1-congenital_disorder_of_glycosylation|not_provided|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation": 2,
    "DOLK-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|DK1-congenital_disorder_of_glycosylation": 1,
    "not_provided|DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype": 5,
    "DOLK-related_disorder|DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype": 2,
    "not_specified|DK1-congenital_disorder_of_glycosylation": 4,
    "not_specified|not_provided|DK1-congenital_disorder_of_glycosylation|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|DK1-congenital_disorder_of_glycosylation": 2,
    "Cardiovascular_phenotype|DOLK-related_disorder|not_specified|not_provided|DK1-congenital_disorder_of_glycosylation": 2,
    "DK1-congenital_disorder_of_glycosylation|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation": 3,
    "Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|DOLK-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|not_specified": 1,
    "DOLK-related_disorder|Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation": 1,
    "not_provided|DK1-congenital_disorder_of_glycosylation|not_specified|Cardiovascular_phenotype": 1,
    "DK1-congenital_disorder_of_glycosylation|not_specified": 1,
    "Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|not_specified|not_provided|DOLK-related_disorder": 1,
    "Cardiovascular_phenotype|DK1-congenital_disorder_of_glycosylation|DOLK-related_disorder": 1,
    "not_provided|DK1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NUP188-related_disorder": 3,
    "not_provided|NUP188-related_disorder|Inborn_genetic_diseases": 1,
    "Sandestig-stefanova_syndrome|not_provided": 3,
    "not_provided|Sandestig-stefanova_syndrome": 3,
    "NUP188-related_disorder": 28,
    "NUP188-related_disorder|not_provided": 9,
    "Sandestig-stefanova_syndrome": 10,
    "NUP188-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|NUP188-related_disorder": 8,
    "Microcephaly|Sandestig-stefanova_syndrome": 2,
    "NUP188-related_disorder|Inborn_genetic_diseases|Sandestig-stefanova_syndrome": 1,
    "Sandestig-stefanova_syndrome|Inborn_genetic_diseases": 1,
    "NUP188-related_disorder|Sandestig-stefanova_syndrome": 1,
    "Inborn_genetic_diseases|NUP188-related_disorder|not_provided": 1,
    "Sandestig-stefanova_syndrome|not_provided|not_specified": 1,
    "NUP188-related_disorder|Sandestig-stefanova_syndrome|not_specified|not_provided": 2,
    "NUP188-related_disorder|Sandestig-stefanova_syndrome|not_provided|not_specified": 1,
    "Neurodegeneration_with_brain_iron_accumulation_8|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation_8": 3,
    "Deficiency_of_carnitine_acetyltransferase|not_provided": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_8": 5,
    "not_provided|CRAT-related_disorder": 3,
    "CRAT-related_disorder": 1,
    "CRAT-related_disorder|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation_8|Neurodegeneration_with_brain_iron_accumulation|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_8|not_specified|not_provided": 2,
    "Deficiency_of_carnitine_acetyltransferase|not_provided|CRAT-related_disorder": 1,
    "Neurodegeneration_with_brain_iron_accumulation_8|not_specified": 1,
    "Parkinson_disease_25|_autosomal_recessive_early-onset|_with_impaired_intellectual_development": 2,
    "Early-onset_generalized_limb-onset_dystonia": 37,
    "Early-onset_generalized_limb-onset_dystonia|not_provided": 7,
    "Dystonic_disorder|Early-onset_generalized_limb-onset_dystonia|not_provided": 1,
    "not_provided|TOR1A-related_disorder": 1,
    "TOR1A-related_disorder|Dystonic_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Dystonic_disorder": 2,
    "Early-onset_generalized_limb-onset_dystonia|Dystonia|_early-onset_atypical|_with_myoclonic_features": 1,
    "not_provided|Early-onset_generalized_limb-onset_dystonia": 3,
    "Arthrogryposis_multiplex_congenita_5|Inborn_genetic_diseases": 1,
    "Arthrogryposis_multiplex_congenita_5": 5,
    "Early-onset_generalized_limb-onset_dystonia|Arthrogryposis_multiplex_congenita_5": 3,
    "Arthrogryposis_multiplex_congenita_5|Early-onset_generalized_limb-onset_dystonia|TOR1A-related_disorder|Dystonic_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TOR1A-related_disorder": 3,
    "TOR1A-related_disorder|Dystonic_disorder|not_provided|Early-onset_generalized_limb-onset_dystonia": 1,
    "Arthrogryposis_multiplex_congenita_5|not_provided|Dystonic_disorder|Early-onset_generalized_limb-onset_dystonia": 1,
    "not_provided|Inborn_genetic_diseases|Early-onset_generalized_limb-onset_dystonia|Dystonic_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Dystonic_disorder": 3,
    "Dystonic_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Early-onset_generalized_limb-onset_dystonia|not_specified|Dystonic_disorder": 2,
    "Early-onset_generalized_limb-onset_dystonia|Dystonic_disorder": 1,
    "Dystonic_disorder|Arthrogryposis_multiplex_congenita_5|not_provided": 1,
    "Inborn_genetic_diseases|Dystonic_disorder|not_provided": 2,
    "Early-onset_generalized_limb-onset_dystonia|Arthrogryposis_multiplex_congenita_5|Dystonic_disorder|not_specified|not_provided|.": 1,
    "Dystonic_disorder|not_specified|not_provided|Dystonia_1|_torsion|_late-onset|Early-onset_generalized_limb-onset_dystonia": 1,
    "not_provided|Dystonic_disorder|Early-onset_generalized_limb-onset_dystonia": 3,
    "Early-onset_generalized_limb-onset_dystonia|Flexion_contracture": 1,
    "Early-onset_generalized_limb-onset_dystonia|Dystonic_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita_5": 1,
    "Citrullinemia_type_I": 148,
    "Citrullinemia_type_I|not_provided": 7,
    "Citrullinemia_type_I|not_specified": 3,
    "Citrullinemia|Citrullinemia_type_I|not_specified": 1,
    "Citrullinemia_type_I|not_specified|Citrullinemia|not_provided": 2,
    "Inborn_genetic_diseases|Citrullinemia_type_I|Citrullinemia": 1,
    "Citrullinemia|not_specified|not_provided|Citrullinemia_type_I": 2,
    "Citrullinemia_type_I|Citrullinemia": 37,
    "Citrullinemia_type_I|Citrullinemia|not_provided": 2,
    "ASS1-related_disorder|Citrullinemia|Citrullinemia_type_I": 2,
    "Citrullinemia|not_specified": 5,
    "Citrullinemia|Inborn_genetic_diseases": 6,
    "Citrullinemia|not_specified|not_provided": 1,
    "Citrullinemia_type_I|Citrullinemia|not_specified|not_provided": 1,
    "Citrullinemia_type_I|Inborn_genetic_diseases|Citrullinemia": 2,
    "Citrullinemia|Citrullinemia_type_I": 51,
    "not_specified|Citrullinemia|Inborn_genetic_diseases|Citrullinemia_type_I": 1,
    "not_specified|Citrullinemia_type_I|Citrullinemia": 5,
    "Citrullinemia_type_I|not_provided|not_specified": 1,
    "not_provided|Citrullinemia_type_I": 6,
    "Citrullinemia|not_specified|Citrullinemia_type_I": 1,
    "Citrullinemia_type_I|not_provided|Citrullinemia|See_cases": 1,
    "Citrullinemia|Citrullinemia_type_I|Inborn_genetic_diseases": 1,
    "Citrullinemia_type_I|not_provided|Citrullinemia": 2,
    "not_provided|Citrullinemia|Citrullinemia_type_I": 3,
    "Citrullinemia_type_I|Inborn_genetic_diseases|Citrullinemia|not_provided": 1,
    "See_cases|Citrullinemia|Citrullinemia_type_I": 1,
    "Citrullinemia|not_provided|Citrullinemia_type_I": 15,
    "Citrullinemia_type_I|Citrullinemia|not_specified": 5,
    "Citrullinemia|Inborn_genetic_diseases|not_provided|not_specified|Citrullinemia_type_I": 1,
    "not_provided|Citrullinemia": 4,
    "not_provided|Citrullinemia_type_I|Citrullinemia|not_specified": 2,
    "Citrullinemia_type_I|not_specified|Citrullinemia": 1,
    "Citrullinemia_type_I|Citrullinemia|_type_II|_adult-onset": 1,
    "not_specified|Citrullinemia|Citrullinemia_type_I": 2,
    "Citrullinemia|ASS1-related_disorder|Citrullinemia_type_I|not_provided": 1,
    "Citrullinemia|ASS1-related_disorder": 1,
    "Citrullinemia|not_provided|Citrullinemia_type_I|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Citrullinemia": 1,
    "Citrullinemia|not_provided|Citrullinemia_type_I|not_specified": 1,
    "not_provided|Citrullinemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Citrullinemia_type_I": 1,
    "ASS1-related_disorder": 5,
    "Citrullinemia_type_I|Citrullinemia|Inborn_genetic_diseases|not_provided": 1,
    "ASS1-related_disorder|Citrullinemia|not_provided|Citrullinemia_type_I|Citrullinemia|_mild": 1,
    "not_provided|ASS1-related_disorder|Citrullinemia": 1,
    "Citrullinemia|not_provided": 4,
    "not_specified|not_provided|Citrullinemia_type_I|Citrullinemia": 1,
    "not_provided|ASS1-related_disorder|Citrullinemia|Citrullinemia_type_I|Inborn_genetic_diseases": 1,
    "Citrullinemia|not_specified|Citrullinemia_type_I|not_provided": 1,
    "Citrullinemia_type_I|not_specified|not_provided|Citrullinemia": 1,
    "not_provided|not_specified|Citrullinemia|Citrullinemia_type_I": 1,
    "Citrullinemia|Inborn_genetic_diseases|Citrullinemia_type_I": 2,
    "not_specified|Citrullinemia_type_I": 2,
    "not_provided|Citrullinemia|Inborn_genetic_diseases|not_specified|ASS1-related_disorder": 1,
    "Citrullinemia_type_I|not_provided|Citrullinemia|not_specified": 1,
    "Inborn_genetic_diseases|Citrullinemia|Citrullinemia_type_I": 1,
    "Citrullinemia|ASS1-related_disorder|Citrullinemia_type_I": 2,
    "Citrullinemia_type_I|See_cases|not_provided|Citrullinemia|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 1,
    "Citrullinemia_type_I|ASS1-related_disorder|Citrullinemia": 1,
    "not_provided|Citrullinemia_type_I|not_specified": 1,
    "not_provided|Citrullinemia_type_I|Citrullinemia": 1,
    "not_specified|Citrullinemia_type_I|Citrullinemia|not_provided": 1,
    "Citrullinemia_type_I|Cardiac_arrhythmia|Citrullinemia": 1,
    "not_specified|not_provided|ASS1-related_disorder|Citrullinemia|Citrullinemia_type_I": 1,
    "not_specified|Citrullinemia|not_provided|Citrullinemia_type_I": 1,
    "not_specified|not_provided|Citrullinemia_type_I": 1,
    "ASS1-related_disorder|Citrullinemia|not_provided|Citrullinemia_type_I": 1,
    "Citrullinemia|not_provided|Citrullinemia_type_I|See_cases": 1,
    "Citrullinemia|Citrullinemia_type_I|not_provided": 2,
    "Citrullinemia|not_provided|Citrullinemia|_mild|Citrullinemia_type_I": 1,
    "Citrullinemia_type_I|Citrullinemia|not_provided|ASS1-related_disorder": 1,
    "not_specified|Citrullinemia|Citrullinemia_type_I|not_provided": 1,
    "not_specified|not_provided|Citrullinemia|Citrullinemia_type_I": 1,
    "Citrullinemia|Inborn_genetic_diseases|not_provided|Citrullinemia_type_I": 1,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome": 194,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome|Inborn_genetic_diseases": 4,
    "not_provided|Inborn_genetic_diseases|Congenital_insensitivity_to_pain-hypohidrosis_syndrome": 2,
    "Inborn_genetic_diseases|Congenital_insensitivity_to_pain-hypohidrosis_syndrome": 17,
    "not_provided|Congenital_insensitivity_to_pain-hypohidrosis_syndrome": 5,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_provided": 5,
    "Inborn_genetic_diseases|Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_provided": 3,
    "not_provided|Congenital_insensitivity_to_pain-hypohidrosis_syndrome|Inborn_genetic_diseases": 4,
    "PRDM12-related_disorder|Congenital_insensitivity_to_pain-hypohidrosis_syndrome": 1,
    "not_provided|PRDM12-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_insensitivity_to_pain-hypohidrosis_syndrome": 1,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_provided|PRDM12-related_disorder": 1,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_specified|not_provided": 1,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome|Hereditary_sensory_and_autonomic_neuropathy": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_provided": 1,
    "Congenital_insensitivity_to_pain-hypohidrosis_syndrome|not_provided|not_specified|PRDM12-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa-hearing_loss-premature_aging-short_stature-facial_dysmorphism_syndrome": 2,
    "not_specified|not_provided|Retinitis_pigmentosa-hearing_loss-premature_aging-short_stature-facial_dysmorphism_syndrome": 1,
    "Retinitis_pigmentosa-hearing_loss-premature_aging-short_stature-facial_dysmorphism_syndrome|not_provided": 2,
    "EXOSC2-related_disorder|not_provided|not_specified": 1,
    "not_provided|EXOSC2-related_disorder": 1,
    "Retinitis_pigmentosa-hearing_loss-premature_aging-short_stature-facial_dysmorphism_syndrome": 2,
    "Retinitis_pigmentosa-hearing_loss-premature_aging-short_stature-facial_dysmorphism_syndrome|Retinal_dystrophy|not_specified|not_provided": 1,
    "Neurodevelopmental_delay|Retinitis_pigmentosa-hearing_loss-premature_aging-short_stature-facial_dysmorphism_syndrome": 1,
    "EXOSC2-related_disorder|not_provided": 1,
    "Congenital_heart_defects_and_skeletal_malformations_syndrome|not_provided": 6,
    "not_specified|not_provided|ABL1-related_disorder": 1,
    "Congenital_heart_defects_and_skeletal_malformations_syndrome": 18,
    "ABL1-related_disorder": 7,
    "Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Congenital_heart_defects_and_skeletal_malformations_syndrome|not_specified|not_provided": 1,
    "not_provided|Congenital_heart_defects_and_skeletal_malformations_syndrome": 5,
    "ABL1-related_disorder|not_provided": 11,
    "Congenital_heart_defects_and_skeletal_malformations_syndrome|not_provided|Failure_to_thrive|Congenital_heart_disease|Abnormal_skeletal_morphology": 1,
    "Leukemia|_Philadelphia_chromosome-positive|_resistant_to_imatinib": 3,
    "ABL1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Congenital_heart_defects_and_skeletal_malformations_syndrome": 1,
    "ABL1-related_congenital_heart_defects_and_skeletal_malformations_syndrome": 1,
    "Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Leukemia|_Philadelphia_chromosome-positive|_resistant_to_imatinib": 1,
    "not_provided|Abnormal_skeletal_morphology|Congenital_heart_disease|Failure_to_thrive|Congenital_heart_defects_and_skeletal_malformations_syndrome": 1,
    "Microcephaly|Congenital_heart_defects_and_skeletal_malformations_syndrome": 1,
    "Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Congenital_heart_defects_and_skeletal_malformations_syndrome": 1,
    "not_provided|ABL1-related_disorder": 6,
    "not_provided|Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Congenital_heart_defects_and_skeletal_malformations_syndrome|not_specified": 1,
    "ABL1-related_disorder|Congenital_heart_defects_and_skeletal_malformations_syndrome|Chronic_myelogenous_leukemia|_BCR-ABL1_positive|not_provided": 1,
    "Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Congenital_heart_defects_and_skeletal_malformations_syndrome|not_provided": 2,
    "not_specified|ABL1-related_disorder|not_provided": 1,
    "Occipital_pachygyria_and_polymicrogyria": 22,
    "not_provided|Occipital_pachygyria_and_polymicrogyria": 17,
    "Occipital_pachygyria_and_polymicrogyria|not_specified|not_provided": 7,
    "not_provided|LAMC3-related_disorder": 16,
    "Occipital_pachygyria_and_polymicrogyria|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Occipital_pachygyria_and_polymicrogyria|Inborn_genetic_diseases": 4,
    "LAMC3-related_disorder|not_provided": 12,
    "LAMC3-related_disorder|not_specified|not_provided": 4,
    "not_provided|Occipital_pachygyria_and_polymicrogyria|not_specified": 2,
    "not_provided|not_specified|Occipital_pachygyria_and_polymicrogyria": 3,
    "not_specified|Occipital_pachygyria_and_polymicrogyria|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|Occipital_pachygyria_and_polymicrogyria": 3,
    "LAMC3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "LAMC3-related_disorder": 3,
    "Occipital_pachygyria_and_polymicrogyria|not_provided": 7,
    "Occipital_pachygyria_and_polymicrogyria|not_provided|not_specified": 7,
    "Inborn_genetic_diseases|Occipital_pachygyria_and_polymicrogyria|not_provided": 1,
    "not_specified|LAMC3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|not_provided|Occipital_pachygyria_and_polymicrogyria|Neonatal_death": 1,
    "LAMC3-related_disorder|not_specified|not_provided|Intellectual_disability": 1,
    "not_specified|not_provided|LAMC3-related_disorder": 6,
    "LAMC3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Occipital_pachygyria_and_polymicrogyria": 1,
    "Inborn_genetic_diseases|not_specified|LAMC3-related_disorder|not_provided": 1,
    "LAMC3-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Neonatal_death": 1,
    "Occipital_pachygyria_and_polymicrogyria|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Occipital_pachygyria_and_polymicrogyria|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Left_ventricular_noncompaction": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|LAMC3-related_disorder": 2,
    "LAMC3-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Left_ventricular_noncompaction|Occipital_pachygyria_and_polymicrogyria": 1,
    "not_provided|LAMC3-related_disorder|Inborn_genetic_diseases": 2,
    "LAMC3-related_disorder|not_specified|not_provided|Occipital_pachygyria_and_polymicrogyria": 1,
    "LAMC3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Left_ventricular_noncompaction|Occipital_pachygyria_and_polymicrogyria": 1,
    "not_provided|Inborn_genetic_diseases|Occipital_pachygyria_and_polymicrogyria": 2,
    "Inborn_genetic_diseases|not_provided|LAMC3-related_disorder|Occipital_pachygyria_and_polymicrogyria": 1,
    "not_provided|not_specified|LAMC3-related_disorder": 1,
    "not_specified|LAMC3-related_disorder|not_provided": 1,
    "not_provided|not_specified|LAMC3-related_disorder|Inborn_genetic_diseases|See_cases": 1,
    "not_provided|Occipital_pachygyria_and_polymicrogyria|not_specified|LAMC3-related_disorder": 1,
    "not_provided|LAMC3-related_disorder|not_specified": 2,
    "Occipital_pachygyria_and_polymicrogyria|Inborn_genetic_diseases": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9|Progressive_microcephaly|Recurrent_encephalopathy": 1,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9": 9,
    "not_specified|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9|Acute_myeloid_leukemia|Acute_lymphoid_leukemia": 2,
    "NUP214-related_disorder": 11,
    "not_provided|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9": 2,
    "NUP214-related_disorder|not_provided": 3,
    "NUP14_Related_Disorders": 2,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9|not_specified": 1,
    "Acute_lymphoid_leukemia|Acute_myeloid_leukemia|Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9": 2,
    "Encephalopathy|_acute|_infection-induced|_susceptibility_to|_9|not_provided": 1,
    "Congenital_anomaly_of_face|Growth_delay|Developmental_delay": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 31,
    "POMT1-related_disorder": 9,
    "Limb-girdle_muscular_dystrophy|_recessive": 6,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 6,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 241,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 105,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 65,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 6,
    "not_provided|POMT1-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 89,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 42,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 5,
    "Dysgenesis_of_the_cerebellar_vermis": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 8,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 45,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided": 8,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified|not_provided": 4,
    "POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 11,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 6,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Dysgenesis_of_the_cerebellar_vermis": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided|POMT1-related_congenital_myopathy|Inborn_genetic_diseases|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "POMT1-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 40,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided": 6,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified": 5,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|POMT1-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 14,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 15,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 6,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 6,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 3,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 5,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|POMT1-related_disorder": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|POMT1-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|POMT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Abnormality_of_the_nervous_system": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 4,
    "POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Limb-girdle_muscular_dystrophy|_recessive|POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 5,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 2,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Inborn_genetic_diseases|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Myopathy_caused_by_variation_in_POMT1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided": 1,
    "POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "POMT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Pyridoxine-dependent_epilepsy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Neurodevelopmental_abnormality|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|POMT1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Abnormality_of_the_musculature|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "not_specified|not_provided|POMT1-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "not_provided|POMT1-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified": 1,
    "POMT1-related_congenital_myopathy|not_provided": 1,
    "Ventriculomegaly|Abnormal_brainstem_morphology|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 2,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|POMT1-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Severe_global_developmental_delay|Seizure|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Limb-girdle_muscular_dystrophy_due_to_POMK_deficiency|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Inborn_genetic_diseases|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|POMT1-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "POMT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 4,
    "not_provided|not_specified|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided": 1,
    "POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified|not_provided": 2,
    "POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 3,
    "POMT1-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 2,
    "Inborn_genetic_diseases|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "POMT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|POMT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|POMT1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Inborn_genetic_diseases": 2,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|POMT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 2,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_provided|Congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Intellectual_disability": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Myopathy_caused_by_variation_in_POMT1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Inborn_genetic_diseases": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|POMT1-related_disorder|not_provided|not_specified": 1,
    "not_specified|POMT1-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Inborn_genetic_diseases|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "POMT1-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Poor_speech|Sensory_neuropathy|Gait_disturbance|Hearing_impairment|Cerebellar_ataxia|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Inborn_genetic_diseases|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided|Inborn_genetic_diseases": 1,
    "FAM157B-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified|not_provided": 1,
    "not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|not_specified": 1,
    "not_specified|not_provided|POMT1-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy|_type_C|POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Ventriculomegaly|Abnormal_brainstem_morphology": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|Inborn_genetic_diseases|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "not_specified|POMT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|POMT1-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_provided": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2K|not_specified|not_provided": 1,
    "not_provided|Monoclonal_B-Cell_Lymphocytosis": 1,
    "not_provided|Severe_myoclonic_epilepsy_in_infancy|Neurodevelopmental_disorder_with_spasticity|_cataracts|_and_cerebellar_hypoplasia": 1,
    "not_provided|Neurodevelopmental_disorder_with_spasticity|_cataracts|_and_cerebellar_hypoplasia": 2,
    "Neurodevelopmental_disorder_with_spasticity|_cataracts|_and_cerebellar_hypoplasia": 5,
    "Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia|Neurodevelopmental_disorder": 4,
    "Stereotypical_hand_wringing|Areflexia|Generalized_hypotonia|Global_developmental_delay|Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia": 1,
    "Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia|Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language": 1,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia": 1,
    "Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia|not_provided": 2,
    "Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia|Developmental_and_epileptic_encephalopathy|_27": 1,
    "not_provided|Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia": 1,
    "Neurodevelopmental_disorder_with_behavioral_abnormalities|_absent_speech|_and_hypotonia": 7,
    "Intellectual_developmental_disorder_with_macrocephaly|_seizures|_and_speech_delay|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia|_seizures|_and_absent_language": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 357,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_Lateral_Sclerosis|_Dominant": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 26,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 19,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 389,
    "Amyotrophic_lateral_sclerosis_type_4|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Amyotrophic_lateral_sclerosis_type_4": 5,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Hereditary_spastic_paraplegia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|not_provided": 14,
    "SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 4,
    "SETX-related_disorder": 37,
    "Inborn_genetic_diseases|SETX-related_disorder|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 42,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided": 5,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 17,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 7,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided": 11,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided": 6,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 4,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|SETX-related_disorder": 6,
    "Amyotrophic_lateral_sclerosis_type_4|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases": 10,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 12,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|not_specified": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided": 24,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 25,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases": 11,
    "SETX-related_disorder|not_provided": 4,
    "not_specified|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Inborn_genetic_diseases|not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|Inborn_genetic_diseases": 6,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder": 3,
    "not_specified|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 3,
    "Proximal_spinal_muscular_atrophy": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases": 36,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|Inborn_genetic_diseases": 2,
    "SETX-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 5,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis": 1,
    "SETX-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "not_provided|SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 4,
    "Inborn_genetic_diseases|SETX-related_disorder|not_specified|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 6,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4": 20,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 34,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|not_provided": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|not_specified|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 11,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided|SETX-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|SETX-related_disorder": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 2,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|SETX-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_provided": 10,
    "SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_4|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 2,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified": 4,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|not_specified": 4,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Amyotrophic_Lateral_Sclerosis|_Dominant|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 2,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder": 6,
    "SETX-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 2,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|SETX-related_disorder": 2,
    "not_provided|SETX-related_disorder": 2,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Distal_spinal_muscular_atrophy": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 4,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 3,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided|SETX-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 3,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Hereditary_spastic_paraplegia|not_specified": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Inborn_genetic_diseases|SETX-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Hereditary_spastic_paraplegia": 2,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|SETX-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder": 3,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 6,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|not_specified": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Cerebral_palsy": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified": 4,
    "SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_provided": 2,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Inborn_genetic_diseases|not_specified|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided|SETX-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Hereditary_spastic_paraplegia": 2,
    "Cerebellar_ataxia|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Amyotrophic_lateral_sclerosis|Abnormal_central_motor_function": 1,
    "not_specified|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder": 1,
    "not_provided|Cerebellar_ataxia|Slightly_reduced_reflexes|Dysdiadochokinesis|Dysmetria|Slurred_speech|Cerebellar_atrophy|Nystagmus|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|See_cases|not_provided": 1,
    "not_provided|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 3,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 2,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder": 3,
    "Inborn_genetic_diseases|SETX-related_disorder|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided": 1,
    "not_specified|SETX-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Inborn_genetic_diseases|not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia|SETX-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|Inborn_genetic_diseases|SETX-related_disorder|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Frontotemporal_dementia": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|SETX-related_disorder|not_provided": 3,
    "SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|SETX-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Hereditary_spastic_paraplegia|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided": 1,
    "SETX-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 2,
    "Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Inborn_genetic_diseases|SETX-related_disorder|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "SETX-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided": 1,
    "not_provided|SETX-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|Inborn_genetic_diseases": 3,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_provided|not_specified": 1,
    "SETX-related_disorder|not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Inborn_genetic_diseases|SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 2,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases": 1,
    "SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Limb-girdle_muscular_dystrophy": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Amyotrophic_lateral_sclerosis": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder|not_provided|Amyotrophic_lateral_sclerosis|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_specified|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_specified|not_provided|SETX-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|SETX-related_disorder|not_specified|not_provided|Cone-rod_dystrophy|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "SETX-related_disorder|not_specified|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases": 1,
    "not_specified|SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 2,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "not_provided|not_specified|SETX-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_provided": 1,
    "Spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Inborn_genetic_diseases|SETX-related_disorder|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|Inborn_genetic_diseases|See_cases": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided|SETX-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Mental_deterioration|Dystonic_disorder": 1,
    "Hereditary_spastic_paraplegia|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|not_specified|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|See_cases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Inborn_genetic_diseases|Tay-Sachs_disease|SETX-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|SETX-related_disorder": 1,
    "SETX-related_disorder|Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 2,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases": 1,
    "Cone-rod_dystrophy|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Hereditary_spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|SETX-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_4": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_specified|Amyotrophic_lateral_sclerosis_type_4": 1,
    "SETX-related_disorder|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Charcot-Marie-Tooth_disease|Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided|Spastic_ataxia": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "SETX-related_disorder|not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|SETX-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "SETX-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|Distal_spinal_muscular_atrophy": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Frontotemporal_dementia|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 3,
    "SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 1,
    "SETX-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided": 1,
    "SETX-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Distal_spinal_muscular_atrophy|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "SETX-related_disorder|Inborn_genetic_diseases|not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided|SETX-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|SETX-related_disorder": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|SETX-related_disorder|not_specified|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Frontotemporal_dementia": 1,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_provided": 1,
    "SETX-related_disorder|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_4|Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|SETX-related_disorder": 1,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|SETX-related_disorder|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Hereditary_spastic_paraplegia": 2,
    "not_provided|Inborn_genetic_diseases|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "Charcot-Marie-Tooth_disease|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2": 1,
    "not_specified|not_provided|SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Hereditary_spastic_paraplegia": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "SETX-related_disorder|Amyotrophic_lateral_sclerosis_type_4|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_2|Amyotrophic_lateral_sclerosis_type_4|not_specified": 1,
    "Distal_spinal_muscular_atrophy|not_provided|Amyotrophic_lateral_sclerosis_type_4": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 23,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 55,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 59,
    "Tuberous_sclerosis_1|not_provided|Isolated_focal_cortical_dysplasia_type_II": 3,
    "Tuberous_sclerosis_syndrome": 1076,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_1": 12,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 4,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 35,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|not_provided": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|not_provided": 4,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Tuberous_sclerosis_1": 1876,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 350,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 6,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 43,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 29,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified|Tuberous_sclerosis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 491,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Acute_myeloid_leukemia": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 97,
    "not_specified|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 28,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 6,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1": 29,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_provided": 2,
    "Tuberous_sclerosis_1|TSC1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 12,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 8,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided": 26,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 8,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "not_specified|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 6,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 32,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 40,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 3,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 7,
    "Tuberous_sclerosis_1|not_provided": 34,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 11,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 3,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder": 1,
    "not_provided|Tuberous_sclerosis_1": 46,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified": 7,
    "not_specified|Tuberous_sclerosis_1": 13,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 8,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 58,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 12,
    "TSC1-related_disorder": 13,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 13,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 15,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 3,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 9,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|not_provided": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 5,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 2,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 26,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 4,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 5,
    "TSC1-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 43,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 30,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 12,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|Tuberous_sclerosis_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|Tuberous_sclerosis_1": 2,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Ovarian_cancer|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1": 7,
    "not_provided|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|TSC1-related_disorder|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 8,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_provided": 1,
    "not_provided|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Epilepsy|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|TSC1-related_disorder|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1": 6,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 12,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 5,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 3,
    "not_provided|Tuberous_sclerosis_syndrome": 55,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 8,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 28,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder": 1,
    "not_specified|Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Ovarian_cancer|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided": 4,
    "Tuberous_sclerosis_syndrome|not_provided": 41,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder": 1,
    "not_provided|Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|TSC1-related_disorder|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 7,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|not_provided|Malignant_tumor_of_urinary_bladder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 5,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 15,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided": 2,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|not_provided|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_specified|Tuberous_sclerosis_1|TSC1-related_disorder": 1,
    "TSC1-related_disorder|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_specified": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 8,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_specified|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|TSC1-related_disorder": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 8,
    "Tuberous_sclerosis_1|not_specified": 11,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder": 5,
    "Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "TSC1-related_disorder|Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_1|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 2,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Multiple_renal_cysts|Cortical_tubers|Seizure|not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC1-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 4,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 4,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_1": 4,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|TSC1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 3,
    "not_specified|not_provided|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided|not_specified": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Tuberous_sclerosis_1": 3,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|Cardiac_rhabdomyoma|Hamartoma|Seizure|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 2,
    "Lymphangiomyomatosis": 20,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis": 4,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_1|not_provided|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC1-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_provided": 2,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 5,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 6,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 2,
    "not_provided|Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|not_specified": 1,
    "Tuberous_sclerosis_syndrome|not_specified|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Focal_cortical_dysplasia_of_Taylor_type_2B|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 7,
    "Tuberous_sclerosis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided": 7,
    "Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|TSC1-related_disorder": 1,
    "Tuberous_sclerosis_syndrome|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|not_specified": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_provided|TSC1-related_disorder": 2,
    "See_cases|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided|Malignant_tumor_of_urinary_bladder": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 5,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified|Tuberous_sclerosis_syndrome": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder": 2,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1": 4,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_1|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder": 2,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC1-related_disorder|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "Tuberous_sclerosis_1|not_provided|Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 4,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|TSC1-related_disorder|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_1": 2,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder": 2,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided": 1,
    "not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_specified|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_1|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 2,
    "Lung_lymphangioleiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|not_specified|not_provided|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|not_provided": 1,
    "not_provided|not_specified|Tuberous_sclerosis_1": 1,
    "not_specified|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|not_provided|TSC1-related_disorder|Isolated_focal_cortical_dysplasia_type_II|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "not_provided|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|TSC1-related_disorder|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Primitive_neuroectodermal_tumor|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|not_specified": 1,
    "not_specified|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Ovarian_cancer|not_specified|not_provided": 1,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|Craniopharyngioma|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Autism_spectrum_disorder|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|not_specified|not_provided|Tuberous_sclerosis_syndrome|Hearing_impairment": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC1-related_disorder|Tuberous_sclerosis_1|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_1": 1,
    "not_provided|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Intellectual_disability": 1,
    "TSC1-related_disorder|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_syndrome|TSC1-related_disorder|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_1": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1": 1,
    "not_provided|Tuberous_sclerosis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Tuberous_sclerosis_syndrome": 4,
    "not_specified|TSC1-related_disorder|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 2,
    "not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_1": 1,
    "not_specified|Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 2,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Craniopharyngioma|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_1|Ovarian_cancer": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Intellectual_disability|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Malignant_tumor_of_urinary_bladder|not_provided|Tuberous_sclerosis_1|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder|not_specified": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|TSC1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|not_specified": 1,
    "Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Autism_spectrum_disorder": 1,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_provided|Tuberous_sclerosis_1|Malignant_tumor_of_urinary_bladder": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Lung_lymphangioleiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|Isolated_focal_cortical_dysplasia_type_II|TSC1-related_disorder|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|TSC1-related_disorder|not_specified|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Lymphangiomyomatosis": 1,
    "not_provided|Renal_insufficiency|Cortical_dysplasia|Renal_cortical_cysts|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|not_provided|Malignant_tumor_of_urinary_bladder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified|Seizure|not_provided": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|not_provided": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|not_specified|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 3,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Kidney_failure|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_1|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Tuberous_sclerosis_1|See_cases|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "not_provided|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder|not_provided|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_1|not_provided|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|not_provided|Tuberous_sclerosis_1": 2,
    "Cortical_tubers|Adenoma_sebaceum": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Keratoconus|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "TSC1-related_disorder|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|not_provided": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_1": 1,
    "not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|TSC1-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|TSC1-related_disorder|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1|not_provided": 1,
    "not_specified|not_provided|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Cleft_palate": 1,
    "Tuberous_sclerosis_1|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Astrocytoma|Kidney_angiomyolipoma|Angiofibromas": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1|TSC1-related_disorder": 1,
    "TSC1-related_disorder|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_syndrome|Autism_spectrum_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC1-related_disorder": 1,
    "Hereditary_cancer|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1": 1,
    "not_provided|not_specified|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|TSC1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_1": 1,
    "not_specified|Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified|TSC1-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Malignant_tumor_of_urinary_bladder|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|not_provided": 1,
    "not_provided|Tuberous_sclerosis_1|TSC1-related_disorder|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|TSC1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|TSC1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1": 1,
    "Tuberous_sclerosis_1|not_specified|Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|TSC1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 6,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_1|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_syndrome|TSC1-related_disorder": 1,
    "not_specified|Tuberous_sclerosis_syndrome": 3,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_1|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "GFI1B-related_disorder|not_provided": 1,
    "GFI1B-related_disorder|not_specified": 2,
    "Platelet-type_bleeding_disorder_17": 14,
    "GFI1B-related_disorder": 6,
    "Inborn_genetic_diseases|GFI1B-related_disorder": 2,
    "not_specified|Platelet-type_bleeding_disorder_17|not_provided": 1,
    "not_specified|Platelet-type_bleeding_disorder_17": 1,
    "not_provided|Platelet-type_bleeding_disorder_17|not_specified": 1,
    "Platelet-type_bleeding_disorder_17|GFI1B-related_disorder": 1,
    "GFI1B-related_disorder|Platelet-type_bleeding_disorder_17": 1,
    "GFI1B-related_disorder|not_provided|not_specified": 1,
    "Thrombocytopenia|Platelet-type_bleeding_disorder_17|not_specified": 1,
    "Storage_pool_disease_of_platelets": 2,
    "Platelet-type_bleeding_disorder_17|Inborn_genetic_diseases": 1,
    "not_provided|GFI1B-related_disorder": 1,
    "Platelet-type_bleeding_disorder_17|not_provided": 2,
    "Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1|Inborn_genetic_diseases": 3,
    "Multisystem_developmental_disorder": 2,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy": 1,
    "Maturity-onset_diabetes_of_the_young_type_8": 98,
    "Inborn_genetic_diseases|Maturity-onset_diabetes_of_the_young_type_8": 9,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_8": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_8": 1,
    "Monogenic_diabetes|not_specified|Maturity-onset_diabetes_of_the_young_type_8|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_8|not_provided": 2,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_8": 14,
    "Inborn_genetic_diseases|Type_2_diabetes_mellitus": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_8|not_specified": 3,
    "Maturity-onset_diabetes_of_the_young_type_8|not_provided": 6,
    "CEL-related_disorder|not_provided": 2,
    "CEL-related_disorder|Maturity-onset_diabetes_of_the_young_type_8": 1,
    "Maturity-onset_diabetes_of_the_young_type_8|Inborn_genetic_diseases": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_8|not_provided": 1,
    "CEL-related_disorder": 1,
    "CEL-related_disorder|not_provided|Maturity-onset_diabetes_of_the_young_type_8": 1,
    "Maturity-onset_diabetes_of_the_young_type_8|Monogenic_diabetes|Transitory_neonatal_diabetes_mellitus|not_specified|not_provided": 1,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_8": 2,
    "Maturity-onset_diabetes_of_the_young_type_8|not_specified": 2,
    "ABO_blood_group_system": 7,
    "ABO-related_disorder": 3,
    "Three_Vessel_Coronary_Disease|not_provided": 3,
    "Severely_weakened_expression_of_A_on_erythrocytes|ABO_blood_group_system": 1,
    "Severely_weakened_expression_of_A_on_erythrocytes": 2,
    "RPL7A-related_condition": 1,
    "not_specified|Leigh_syndrome": 40,
    "Inborn_genetic_diseases|Leigh_syndrome": 11,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K": 1,
    "Leigh_syndrome|Inborn_genetic_diseases": 13,
    "not_provided|not_specified|SURF1-related_disorder|Leigh_syndrome": 1,
    "not_provided|Leigh_syndrome|SURF1-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Leigh_syndrome|SURF1-related_disorder": 7,
    "SURF1-related_disorder|Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cerebellar_ataxia|Abnormal_pyramidal_sign|Dysarthria|Muscle_weakness|Leigh_syndrome_due_to_mitochondrial_complex_IV_deficiency|Inborn_genetic_diseases|not_provided|Leigh_syndrome|See_cases": 1,
    "Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 9,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|Leigh_syndrome": 9,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Leigh_syndrome": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4K|Leigh_syndrome": 1,
    "Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 20,
    "not_provided|Leigh_syndrome|Inborn_genetic_diseases": 2,
    "Leigh_syndrome|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|not_provided": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome|Charcot-Marie-Tooth_disease_type_4K|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "not_specified|not_provided|Leigh_syndrome": 9,
    "not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cerebellar_ataxia|Abnormal_pyramidal_sign|Dysarthria|Muscle_weakness|Charcot-Marie-Tooth_disease_type_4K": 1,
    "Leigh_syndrome|Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_disease|Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 41,
    "not_provided|Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 3,
    "Leigh_syndrome|Charcot-Marie-Tooth_disease_type_4K": 2,
    "SURF1-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|Leigh_syndrome|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified": 1,
    "Inborn_genetic_diseases|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Mitochondrial_disease|Leigh_syndrome": 1,
    "not_specified|Leigh_syndrome|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K": 1,
    "not_specified|Leigh_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K": 3,
    "not_specified|Leigh_syndrome|not_provided": 4,
    "Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K": 2,
    "Leigh_syndrome|Charcot-Marie-Tooth_disease_type_4K|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 3,
    "Charcot-Marie-Tooth_disease_type_4K": 1,
    "Leigh_syndrome|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 3,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|Inborn_genetic_diseases|not_provided|Leigh_syndrome": 1,
    "SURF1-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|not_provided|Leigh_syndrome": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4K|See_cases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K": 1,
    "Inborn_genetic_diseases|Leigh_syndrome|not_provided": 2,
    "SURF1-related_disorder|Leigh_syndrome": 2,
    "Leigh_syndrome|not_provided|not_specified": 2,
    "Leigh_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Charcot-Marie-Tooth_disease_type_4K|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|Leigh_syndrome|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4K|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome|Charcot-Marie-Tooth_disease_type_4K": 1,
    "not_specified|Leigh_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Leigh_syndrome": 2,
    "not_provided|not_specified|Leigh_syndrome": 1,
    "STKLD1-related_disorder": 5,
    "STKLD1-related_disorder|not_specified": 1,
    "Recurrent_spontaneous_abortion|not_provided": 1,
    "Upshaw-Schulman_syndrome|not_provided": 63,
    "Upshaw-Schulman_syndrome": 209,
    "not_provided|Upshaw-Schulman_syndrome": 46,
    "Upshaw-Schulman_syndrome|not_specified|not_provided": 9,
    "Upshaw-Schulman_syndrome|not_specified|Inborn_genetic_diseases": 2,
    "ADAMTS13-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|not_specified|Upshaw-Schulman_syndrome": 1,
    "Thrombotic_thrombocytopenic_purpura": 3,
    "ADAMTS13-related_disorder": 13,
    "Upshaw-Schulman_syndrome|Inborn_genetic_diseases": 9,
    "not_provided|not_specified|Upshaw-Schulman_syndrome": 4,
    "Inborn_genetic_diseases|Upshaw-Schulman_syndrome": 9,
    "ADAMTS13-related_disorder|not_specified": 1,
    "Upshaw-Schulman_syndrome|not_provided|not_specified": 10,
    "Upshaw-Schulman_syndrome|ADAMTS13-related_disorder|not_specified": 1,
    "not_provided|Upshaw-Schulman_syndrome|not_specified": 3,
    "not_provided|Upshaw-Schulman_syndrome|Inborn_genetic_diseases": 4,
    "not_specified|ADAMTS13-related_disorder|Upshaw-Schulman_syndrome|not_provided": 1,
    "not_specified|not_provided|Upshaw-Schulman_syndrome": 5,
    "not_provided|ADAMTS13-related_disorder|not_specified|Upshaw-Schulman_syndrome": 1,
    "not_provided|Upshaw-Schulman_syndrome|ADAMTS13-related_disorder": 1,
    "Thrombotic_thrombocytopenic_purpura|not_provided": 3,
    "Upshaw-Schulman_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|ADAMTS13-related_disorder": 6,
    "Upshaw-Schulman_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Upshaw-Schulman_syndrome|not_provided": 8,
    "not_provided|not_specified|Inborn_genetic_diseases|ADAMTS13-related_disorder|Upshaw-Schulman_syndrome": 1,
    "Inborn_genetic_diseases|Upshaw-Schulman_syndrome|not_provided": 4,
    "Upshaw-Schulman_syndrome|not_specified|not_provided|See_cases": 1,
    "not_specified|Upshaw-Schulman_syndrome|ADAMTS13-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Upshaw-Schulman_syndrome|not_provided|ADAMTS13-related_disorder": 1,
    "not_provided|not_specified|ADAMTS13-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Upshaw-Schulman_syndrome": 4,
    "Upshaw-Schulman_syndrome|ADAMTS13-related_disorder|not_provided": 2,
    "Upshaw-Schulman_syndrome|ADAMTS13-related_disorder|not_provided|not_specified": 1,
    "ADAMTS13-related_disorder|Inborn_genetic_diseases|not_provided|Upshaw-Schulman_syndrome": 1,
    "ADAMTS13-related_disorder|not_provided|Upshaw-Schulman_syndrome": 3,
    "ADAMTS13-related_disorder|Thrombus|not_provided|Upshaw-Schulman_syndrome": 1,
    "ADAMTS13-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Upshaw-Schulman_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|ADAMTS13-related_disorder": 1,
    "ADAMTS13-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Upshaw-Schulman_syndrome|Thrombotic_thrombocytopenic_purpura": 1,
    "not_provided|not_specified|ADAMTS13-related_disorder|Upshaw-Schulman_syndrome": 1,
    "ADAMTS13-related_disorder|Thrombotic_thrombocytopenic_purpura|not_provided|Upshaw-Schulman_syndrome": 1,
    "not_provided|ADAMTS13-related_disorder|Upshaw-Schulman_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Upshaw-Schulman_syndrome": 1,
    "Upshaw-Schulman_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Thrombotic_thrombocytopenic_purpura|not_provided|Upshaw-Schulman_syndrome": 1,
    "Upshaw-Schulman_syndrome|See_cases|not_provided": 1,
    "Upshaw-Schulman_syndrome|ADAMTS13-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Upshaw-Schulman_syndrome": 1,
    "Upshaw-Schulman_syndrome|not_specified|Three_Vessel_Coronary_Disease|not_provided": 1,
    "ADAMTS13-related_disorder|not_specified|not_provided": 1,
    "Congenital_nonprogressive_myopathy_with_Moebius_and_Robin_sequences": 7,
    "MYMK-related_disorder": 1,
    "Carey-Fineman-Ziter_syndrome_1": 1,
    "Congenital_nonprogressive_myopathy_with_Moebius_and_Robin_sequences|not_provided": 2,
    "Carey-Fineman-Ziter_syndrome_1|Inborn_genetic_diseases": 1,
    "Congenital_nonprogressive_myopathy_with_Moebius_and_Robin_sequences|See_cases": 1,
    "Carey-Fineman-Ziter_syndrome_1|MYMK-related_disorder|Congenital_nonprogressive_myopathy_with_Moebius_and_Robin_sequences|not_provided": 1,
    "not_provided|Congenital_nonprogressive_myopathy_with_Moebius_and_Robin_sequences": 2,
    "MYMK-related_disorder|Carey-Fineman-Ziter_syndrome_1": 1,
    "Geleophysic_dysplasia": 2,
    "not_provided|Lethal_short-limb_skeletal_dysplasia|_Al_Gazali_type": 2,
    "not_provided|Geleophysic_dysplasia_1": 10,
    "Geleophysic_dysplasia_1": 102,
    "Geleophysic_dysplasia_1|ADAMTSL2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|ADAMTSL2-related_disorder": 2,
    "ADAMTSL2-related_disorder": 11,
    "Lethal_short-limb_skeletal_dysplasia|_Al_Gazali_type": 9,
    "Geleophysic_dysplasia_1|not_provided": 15,
    "Geleophysic_dysplasia_1|not_specified|not_provided": 3,
    "Geleophysic_dysplasia_1|Lethal_short-limb_skeletal_dysplasia|_Al_Gazali_type": 2,
    "Geleophysic_dysplasia|not_provided|Geleophysic_dysplasia_1": 1,
    "Inborn_genetic_diseases|not_provided|ADAMTSL2-related_disorder": 1,
    "ADAMTSL2-related_disorder|not_provided|Geleophysic_dysplasia_1": 1,
    "Geleophysic_dysplasia_1|ADAMTSL2-related_disorder": 3,
    "Geleophysic_dysplasia_1|Abnormal_facial_shape": 1,
    "not_specified|not_provided|Geleophysic_dysplasia_1": 1,
    "ADAMTSL2-related_disorder|Geleophysic_dysplasia_1": 1,
    "not_provided|Geleophysic_dysplasia_1|Inborn_genetic_diseases": 1,
    "not_provided|Geleophysic_dysplasia_1|not_specified": 6,
    "Lethal_short-limb_skeletal_dysplasia|_Al_Gazali_type|Geleophysic_dysplasia_1": 1,
    "not_specified|Geleophysic_dysplasia_1|not_provided": 5,
    "Inborn_genetic_diseases|Geleophysic_dysplasia": 1,
    "not_specified|Geleophysic_dysplasia_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Geleophysic_dysplasia_1": 2,
    "Connective_tissue_dysplasia|not_specified|not_provided|Geleophysic_dysplasia_1": 1,
    "Geleophysic_dysplasia_1|Inborn_genetic_diseases": 1,
    "not_provided|ADAMTSL2-related_disorder|Inborn_genetic_diseases": 1,
    "Geleophysic_dysplasia_1|Inborn_genetic_diseases|ADAMTSL2-related_disorder": 1,
    "Geleophysic_dysplasia_1|not_specified": 1,
    "Geleophysic_dysplasia|not_provided": 1,
    "DBH-related_disorder": 1,
    "Dopamine_beta-hydroxylase_polymorphism": 1,
    "Orthostatic_hypotension_1": 324,
    "Inborn_genetic_diseases|Orthostatic_hypotension_1": 22,
    "Orthostatic_hypotension_1|not_specified|not_provided": 1,
    "Orthostatic_hypotension_1|Inborn_genetic_diseases": 25,
    "not_provided|Orthostatic_hypotension_1": 19,
    "not_provided|DBH-related_disorder|Orthostatic_hypotension_1": 2,
    "Orthostatic_hypotension_1|not_provided": 11,
    "Orthostatic_hypotension_1|DBH-related_disorder": 7,
    "not_specified|Orthostatic_hypotension_1|not_provided": 1,
    "Orthostatic_hypotension_1|not_provided|DBH-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Orthostatic_hypotension_1": 1,
    "DBH-related_disorder|not_provided|Orthostatic_hypotension_1": 1,
    "DBH-related_disorder|Orthostatic_hypotension_1": 4,
    "DBH-related_disorder|Orthostatic_hypotension_1|not_provided": 3,
    "Orthostatic_hypotension_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Orthostatic_hypotension_1|DBH-related_disorder": 1,
    "SARDH-related_disorder": 16,
    "SARDH-related_disorder|not_provided": 3,
    "Sarcosine_dehydrogenase_deficiency": 6,
    "not_provided|SARDH-related_disorder": 4,
    "not_specified|Sarcosine_dehydrogenase_deficiency": 1,
    "not_provided|Sarcosine_dehydrogenase_deficiency": 1,
    "Sarcosine_dehydrogenase_deficiency|not_provided": 1,
    "Sarcosine_dehydrogenase_deficiency|not_specified": 1,
    "WDR5-related_neurodevelopmental_delay": 1,
    "RNU6ATAC-associated_neurodevelopmental_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided": 1,
    "Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|COL5A1-related_disorder": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "COL5A1-related_disorder": 22,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified": 6,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Abnormal_bleeding|Thrombocytopenia": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1": 5,
    "not_provided|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Marfan_syndrome": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_provided|not_specified": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome_type_7A": 3,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|See_cases": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 3,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 4,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 10,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cataract|Pneumothorax|Congenital_hip_dislocation|Constrictive_median_neuropathy|Pain|Patellar_dislocation|Gastroesophageal_reflux|Mitral_valve_prolapse|Soft_skin|Bruising_susceptibility|Abnormally_lax_or_hyperextensible_skin|Inguinal_hernia|Difficulty_walking": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_2": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided|COL5A1-related_disorder|Confusion": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal": 8,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided": 29,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 3,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|COL5A1-related_disorder": 2,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided|not_specified": 4,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided": 1,
    "Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "not_specified|not_provided|Fibromuscular_dysplasia|_multifocal|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Abnormal_bleeding": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided": 2,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Fibromuscular_dysplasia|_multifocal|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|not_provided": 11,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiac_arrhythmia|Hyperextensible_hand_joints|Arthralgia|Wolff-Parkinson-White_pattern|Joint_laxity|Joint_dislocation|See_cases|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Fibromuscular_dysplasia|_multifocal|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 2,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Fibromuscular_dysplasia|_multifocal": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|COL5A1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Hypoparathyroidism|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 3,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 10,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 3,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "COL5A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type": 2,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Aortic_dilatation|not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "not_provided|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided": 2,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_provided": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "COL5A1-related_disorder|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 2,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome_type_7A|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_specified|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 3,
    "Thoracic_aortic_aneurysm_or_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Cardiovascular_phenotype|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome_type_7A": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Fibromuscular_dysplasia|_multifocal|not_specified": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided": 4,
    "Clubfoot|Edema_of_the_dorsum_of_feet|Joint_hyperflexibility|Joint_hypermobility|Cutis_laxa|Bilateral_talipes_equinovarus|Hyperextensible_skin|Soft_skin|Bruising_susceptibility|Atrophic_scars": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|See_cases": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type": 1,
    "not_provided|not_specified|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "Connective_tissue_disorder|COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type": 1,
    "not_provided|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "not_specified|Connective_tissue_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|COL5A1-related_disorder": 2,
    "Venous_malformation|Dural_ectasia|Abnormal_digit_morphology|Hypertelorism|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Abnormal_bleeding": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 3,
    "Ehlers-Danlos_syndrome|_classic_type|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome_type_7A": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|not_specified|not_provided": 1,
    "COL5A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|See_cases": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|COL5A1-related_disorder|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_provided|Fibromuscular_dysplasia|_multifocal": 1,
    "not_provided|COL5A1-related_disorder": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome_type_7A": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_2|Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome": 2,
    "COL5A1-related_disorders": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Neurodevelopmental_disorder_with_or_without_autism_or_seizures": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_classic_type|_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Fibromuscular_dysplasia|_multifocal|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Fibromuscular_dysplasia|_multifocal|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "not_specified|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Loeys-Dietz_syndrome|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Cardiovascular_phenotype|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1": 2,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "COL5A1-related_disorder|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|_1|not_provided": 1,
    "COL5A1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|_classic_type|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|not_specified|Ehlers-Danlos_syndrome|_classic_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Connective_tissue_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome_type_7A": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|Fibromuscular_dysplasia|_multifocal": 1,
    "Hyperextensible_skin|Cigarette-paper_scars|Atrophic_scars|Large_joint_dislocations|Joint_hypermobility": 1,
    "Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome|_classic_type|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "COL5A1-related_disorder|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL5A1-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_specified|not_provided|COL5A1-related_disorder": 1,
    "Skeletal_dysplasia|Narrow_chest|Abnormality_of_the_lower_limb|Relative_macrocephaly|Neuropathic_spinal_arthropathy|Scoliosis|not_provided|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_classic_type|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Shoulder_subluxation": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|Fibromuscular_dysplasia|_multifocal|not_specified|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|not_specified": 1,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type": 9,
    "not_provided|Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|_classic_type": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal": 2,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "not_provided|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1": 1,
    "Ehlers-Danlos_syndrome|_classic_type|not_provided|Ehlers-Danlos_syndrome_type_7A|Fibromuscular_dysplasia|_multifocal|Ehlers-Danlos_syndrome|_classic_type|_1|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome_type_7A|Ehlers-Danlos_syndrome|not_provided": 1,
    "Ehlers-Danlos_syndrome_type_7A|not_provided|Ehlers-Danlos_syndrome|_classic_type": 2,
    "FCN2-related_disorder": 3,
    "FCN1-related_disorder": 6,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_36": 1,
    "MRPS2-related_disorder|not_provided": 4,
    "not_specified|MRPS2-related_disorder|not_provided": 1,
    "MRPS2-related_disorder": 7,
    "Combined_oxidative_phosphorylation_deficiency_36": 8,
    "Combined_oxidative_phosphorylation_deficiency_36|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_36|not_specified": 2,
    "not_provided|MRPS2-related_disorder": 1,
    "not_provided|not_specified|MRPS2-related_disorder": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_36|MRPS2-related_disorder": 1,
    "not_provided|SOHLH1-related_disorder|not_specified": 1,
    "SOHLH1-related_disorder": 2,
    "Ovarian_dysgenesis_5|Spermatogenic_failure_32": 3,
    "Spermatogenic_failure_32": 1,
    "Ovarian_dysgenesis_5|Nonsyndromic_hypergonadotropic_hypogonadism": 2,
    "SOHLH1-related_disorder|not_provided": 2,
    "not_specified|SOHLH1-related_disorder": 1,
    "Ovarian_dysgenesis_5": 1,
    "Ovarian_dysgenesis_5|not_provided|Spermatogenic_Failure|Spermatogenic_failure_32": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases": 36,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1263,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 45,
    "Developmental_and_epileptic_encephalopathy|_14": 33,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 8,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified|not_provided": 5,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 64,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 17,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 121,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 58,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|not_provided": 9,
    "KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 7,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 63,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified": 11,
    "KCNT1-related_disorder": 6,
    "KCNT1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|not_provided": 2,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 14,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|not_specified|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|Inborn_genetic_diseases": 4,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|Developmental_and_epileptic_encephalopathy|_14|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Developmental_and_epileptic_encephalopathy_97": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|not_specified": 3,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 5,
    "not_specified|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|See_cases|not_specified|KCNT1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_14|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided": 5,
    "not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 29,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|not_specified": 5,
    "not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 8,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 3,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Developmental_and_epileptic_encephalopathy|_14": 4,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|See_cases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|not_provided": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_14": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 7,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Malignant_migrating_partial_seizures_of_infancy": 1,
    "Inborn_genetic_diseases|KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Inborn_genetic_diseases": 8,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Epilepsy": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 9,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified|Inborn_genetic_diseases": 3,
    "KCNT1-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified|not_provided": 4,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|not_provided": 10,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|not_specified|KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|See_cases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided": 16,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|KCNT1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases": 5,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 2,
    "KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 1,
    "Epilepsy_syndrome|KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|Seizure": 1,
    "not_provided|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided": 2,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|See_cases": 1,
    "KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder|not_provided": 2,
    "Hydrocephalus|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Developmental_and_epileptic_encephalopathy|_15|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_channelopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|not_specified": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Malignant_migrating_partial_seizures_of_infancy": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|KCNT1-related_disorder": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|not_provided|KCNT1-related_disorder|Inborn_genetic_diseases": 1,
    "KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 2,
    "Developmental_and_epileptic_encephalopathy|_14|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 3,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "KCNT1-related_disorder|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|KCNT1-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|not_specified|KCNT1-related_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14": 4,
    "not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 2,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|KCNT1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|Epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|See_cases|Hearing_impairment": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 1,
    "KCNT1-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 2,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 3,
    "not_specified|KCNT1-related_disorder": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|KCNT1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|KCNT1-related_disorder": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Seizure": 1,
    "Malignant_migrating_partial_seizures_of_infancy": 1,
    "Seizure|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Neurodevelopmental_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Focal_epilepsy|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|Malignant_migrating_partial_seizures_of_infancy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_disorder|not_specified": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_disorder": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_14|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_disorder|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "Morphological_central_nervous_system_abnormality": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 2,
    "not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 1,
    "KCNT1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_disorder|not_provided|not_specified": 1,
    "KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|Developmental_and_epileptic_encephalopathy|_14": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5": 1,
    "KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|KCNT1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|KCNT1-related_disorder": 1,
    "Inborn_genetic_diseases|KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Inborn_genetic_diseases|KCNT1-related_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14": 1,
    "Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|KCNT1-related_disorder|Developmental_and_epileptic_encephalopathy|_14|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_14|KCNT1-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_5|Developmental_and_epileptic_encephalopathy|_14|not_provided|KCNT1-related_disorder": 1,
    "CAMSAP1-related_neuronal_migration_disorder|not_provided": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_12|CAMSAP1-related_neuronal_migration_disorder|not_provided": 2,
    "CAMSAP1-related_neuronal_migration_disorder|Cortical_dysplasia|_complex|_with_other_brain_malformations_12": 2,
    "CAMSAP1-related_neuronal_migration_disorder|Cortical_dysplasia|_complex|_with_other_brain_malformations_12|not_provided": 1,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 104,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|not_provided": 15,
    "not_specified|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|not_provided": 2,
    "Inborn_genetic_diseases|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 1,
    "LHX3-related_disorder|Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_1|not_provided": 1,
    "Inborn_genetic_diseases|Combined_Pituitary_Hormone_Deficiency|_Recessive": 1,
    "not_provided|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 10,
    "not_specified|not_provided|Inborn_genetic_diseases|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided|not_specified|LHX3-related_disorder|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 2,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form": 2,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|Inborn_genetic_diseases": 1,
    "not_provided|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Combined_pituitary_hormone_deficiencies|_genetic_form": 1,
    "not_provided|LHX3-related_disorder|Combined_pituitary_hormone_deficiencies|_genetic_form|not_specified": 1,
    "not_provided|LHX3-related_disorder": 1,
    "Combined_pituitary_hormone_deficiencies|_genetic_form|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 1,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|not_provided|LHX3-related_disorder": 1,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|Combined_pituitary_hormone_deficiencies|_genetic_form|not_specified|not_provided": 1,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|Combined_pituitary_hormone_deficiencies|_genetic_form|not_provided": 1,
    "Pituitary_hormone_deficiency|_combined|_1|Inborn_genetic_diseases": 1,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|LHX3-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Combined_pituitary_hormone_deficiencies|_genetic_form|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 2,
    "not_provided|not_specified|Combined_pituitary_hormone_deficiencies|_genetic_form|Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities": 1,
    "Non-acquired_combined_pituitary_hormone_deficiency_with_spine_abnormalities|Combined_pituitary_hormone_deficiencies|_genetic_form|Inborn_genetic_diseases": 1,
    "LHX3-related_disorder": 1,
    "not_specified|not_provided|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 1,
    "Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 451,
    "Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency|CARD9-related_disorder": 4,
    "Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency|Inborn_genetic_diseases": 21,
    "Inborn_genetic_diseases|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 25,
    "Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency|not_provided": 11,
    "CARD9-related_disorder|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 6,
    "not_provided|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 9,
    "not_provided|CARD9-related_disorder|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 1,
    "CARD9-related_disorder|not_provided|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 2,
    "Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency": 1,
    "not_provided|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency|CARD9-related_disorder": 1,
    "not_specified|Predisposition_to_invasive_fungal_disease_due_to_CARD9_deficiency|not_provided": 3,
    "Neurodevelopmental_disorder_with_motor_regression|_progressive_spastic_paraplegia|_and_oromotor_dysfunction": 8,
    "SNAPC4_related_condition": 2,
    "PMPCA-related_disorder|not_provided": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_2": 13,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_2": 2,
    "not_provided|PMPCA-related_disorder": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_2": 3,
    "Autosomal_recessive_spinocerebellar_ataxia_2|not_provided": 5,
    "Autosomal_recessive_spinocerebellar_ataxia_2|PMPCA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Normal_pressure_hydrocephalus|Diffuse_cerebellar_atrophy|Global_brain_atrophy|Chronic_lactic_acidosis|Restrictive_external_ophthalmoplegia|Floppy_infant|Severe_global_developmental_delay|Bilateral_ptosis|Hypoventilation|Blindness|Optic_atrophy|Failure_to_thrive|Hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_2|Normal_pressure_hydrocephalus|Diffuse_cerebellar_atrophy|Global_brain_atrophy|Chronic_lactic_acidosis|Restrictive_external_ophthalmoplegia|Floppy_infant|Severe_global_developmental_delay|Bilateral_ptosis|Hypoventilation|Blindness|Optic_atrophy|Failure_to_thrive|Hypertrophic_cardiomyopathy": 1,
    "PMPCA-related_disorder": 1,
    "Joubert_syndrome_1|not_provided": 3,
    "INPP5E-related_disorder|MORM_syndrome|Joubert_syndrome_1": 1,
    "INPP5E-related_disorder|Joubert_syndrome": 41,
    "Joubert_syndrome_1|MORM_syndrome": 38,
    "INPP5E-related_disorder": 50,
    "Joubert_syndrome|Inborn_genetic_diseases|INPP5E-related_disorder|not_provided": 2,
    "Joubert_syndrome|INPP5E-related_disorder": 33,
    "MORM_syndrome|Joubert_syndrome_1": 2,
    "Joubert_syndrome|not_provided|not_specified|INPP5E-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_and_related_disorders|Rod-cone_dystrophy|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome_1|MORM_syndrome|not_provided|Joubert_syndrome|Rod-cone_dystrophy": 1,
    "not_provided|INPP5E-related_disorder": 1,
    "not_provided|not_specified|Joubert_syndrome_1|Joubert_syndrome": 1,
    "not_specified|not_provided|Joubert_syndrome_1|Joubert_syndrome": 1,
    "not_provided|not_specified|MORM_syndrome|Joubert_syndrome|Joubert_syndrome_1": 1,
    "INPP5E-related_disorder|MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome": 2,
    "Joubert_syndrome|not_provided|Retinal_dystrophy|Rod-cone_dystrophy": 1,
    "INPP5E-related_disorder|Joubert_syndrome|Rod-cone_dystrophy": 1,
    "Joubert_syndrome_1|MORM_syndrome|INPP5E-related_disorder|Joubert_syndrome": 2,
    "INPP5E-related_disorder|Joubert_syndrome_1|MORM_syndrome": 3,
    "Joubert_syndrome_1|INPP5E-related_disorder|not_provided|Joubert_syndrome|Rod-cone_dystrophy": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome|INPP5E-related_disorder": 1,
    "Inborn_genetic_diseases|MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome": 2,
    "not_specified|Joubert_syndrome|INPP5E-related_disorder": 2,
    "not_specified|Joubert_syndrome|Joubert_syndrome_1": 1,
    "not_provided|INPP5E-related_disorder|Joubert_syndrome|Inborn_genetic_diseases|Joubert_syndrome_1|MORM_syndrome": 1,
    "INPP5E-related_disorder|Joubert_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Optic_atrophy|Joubert_syndrome_1|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|MORM_syndrome|Joubert_syndrome_1": 1,
    "Joubert_syndrome_1|MORM_syndrome|INPP5E-related_disorder|Inborn_genetic_diseases|Joubert_syndrome": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_1": 1,
    "MORM_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "MORM_syndrome|Joubert_syndrome_1|Rod-cone_dystrophy|Joubert_syndrome": 1,
    "Joubert_syndrome_1|MORM_syndrome|not_specified|not_provided|Joubert_syndrome": 2,
    "Joubert_syndrome|Joubert_syndrome_1": 6,
    "Joubert_syndrome|INPP5E-related_disorder|Joubert_syndrome_1|MORM_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome|INPP5E-related_disorder": 2,
    "not_provided|INPP5E-related_disorder|Joubert_syndrome_1": 1,
    "Joubert_syndrome|INPP5E-related_disorder|not_provided": 1,
    "Joubert_syndrome|Rod-cone_dystrophy|not_provided": 1,
    "INPP5E-related_disorder|Joubert_syndrome_and_related_disorders|Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome": 1,
    "not_specified|not_provided|Joubert_syndrome_1|INPP5E-related_disorder|Joubert_syndrome": 1,
    "MORM_syndrome|Joubert_syndrome_1|not_specified|Joubert_syndrome": 1,
    "Joubert_syndrome_1|MORM_syndrome|Joubert_syndrome": 4,
    "Inborn_genetic_diseases|Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome": 1,
    "MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Joubert_syndrome_1|INPP5E-related_disorder|MORM_syndrome": 1,
    "not_provided|Joubert_syndrome_1|Joubert_syndrome": 1,
    "not_specified|Joubert_syndrome|MORM_syndrome|Joubert_syndrome_1|not_provided": 1,
    "Joubert_syndrome_1|MORM_syndrome|Joubert_syndrome|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Joubert_syndrome_1|Joubert_syndrome|not_specified|not_provided": 2,
    "Joubert_syndrome_1|MORM_syndrome|not_provided|Joubert_syndrome|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "INPP5E-related_disorder|Inborn_genetic_diseases|Joubert_syndrome": 2,
    "not_specified|Inborn_genetic_diseases|Retinal_dystrophy|Joubert_syndrome|INPP5E-related_disorder": 1,
    "INPP5E-related_disorder|Joubert_syndrome|not_provided|MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome_and_related_disorders|Rod-cone_dystrophy": 1,
    "INPP5E-related_disorder|Joubert_syndrome|Joubert_syndrome_1": 7,
    "MORM_syndrome|Joubert_syndrome_1|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|INPP5E-related_disorder": 3,
    "Joubert_syndrome_1|MORM_syndrome|not_provided|Joubert_syndrome|INPP5E-related_disorder|Rod-cone_dystrophy|Retinal_dystrophy": 1,
    "MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome|not_specified|Rod-cone_dystrophy": 1,
    "MORM_syndrome|Joubert_syndrome_1|Inborn_genetic_diseases|INPP5E-related_disorder|not_specified|not_provided|Joubert_syndrome": 1,
    "not_specified|Joubert_syndrome_1|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|not_specified|INPP5E-related_disorder": 1,
    "INPP5E-related_disorder|Joubert_syndrome|MORM_syndrome|Joubert_syndrome_1": 1,
    "Joubert_syndrome|Joubert_syndrome_1|not_specified": 1,
    "Joubert_syndrome|INPP5E-related_disorder|Inborn_genetic_diseases": 5,
    "not_specified|Joubert_syndrome|Joubert_syndrome_1|not_provided": 2,
    "INPP5E-related_disorder|Retinal_dystrophy": 1,
    "Joubert_syndrome_1|MORM_syndrome|Inborn_genetic_diseases|Joubert_syndrome": 1,
    "INPP5E-related_disorder|Joubert_syndrome|not_provided|Joubert_syndrome_1|Inborn_genetic_diseases": 1,
    "INPP5E-related_disorder|not_specified|Joubert_syndrome|not_provided|Joubert_syndrome_1|Retinal_dystrophy|MORM_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_and_related_disorders|Joubert_syndrome_1|INPP5E-related_disorder": 1,
    "INPP5E-related_disorder|Joubert_syndrome|not_provided|not_specified": 1,
    "not_specified|MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome|not_provided": 1,
    "MORM_syndrome|Joubert_syndrome": 1,
    "Rod-cone_dystrophy|Joubert_syndrome": 2,
    "not_provided|MORM_syndrome|Joubert_syndrome|Joubert_syndrome_1|not_specified": 1,
    "INPP5E-related_disorder|not_specified|not_provided|Joubert_syndrome_1|Joubert_syndrome": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|MORM_syndrome|Joubert_syndrome_1": 2,
    "not_provided|INPP5E-related_disorder|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_1|not_specified|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome|Retinal_dystrophy|not_specified": 1,
    "Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_1|MORM_syndrome|not_specified|not_provided|Joubert_syndrome|Retinal_dystrophy": 1,
    "INPP5E-related_disorder|Clubfoot|Preaxial_foot_polydactyly|Skeletal_dysplasia|Chronic_lung_disease|Absent_epiphyses|Short_femur|Hemivertebrae|Patent_ductus_arteriosus|Cleft_palate|Vertebral_hypoplasia|Abnormal_pulmonary_interstitial_morphology|Coat_hanger_sign_of_ribs|Vertebral_segmentation_defect|Micrognathia|Pseudoarthrosis|Respiratory_failure|Joubert_syndrome_and_related_disorders|Inborn_genetic_diseases|Joubert_syndrome_1|MORM_syndrome|not_provided|Joubert_syndrome": 1,
    "INPP5E-related_disorder|not_provided": 2,
    "MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome": 5,
    "Joubert_syndrome|Rod-cone_dystrophy": 1,
    "not_specified|Joubert_syndrome_1|MORM_syndrome|Joubert_syndrome": 1,
    "MORM_syndrome|Joubert_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Joubert_syndrome|Joubert_syndrome_1": 2,
    "not_provided|INPP5E-related_disorder|MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome": 1,
    "not_specified|MORM_syndrome|not_provided|Joubert_syndrome|Joubert_syndrome_1": 1,
    "Joubert_syndrome|not_provided|Joubert_syndrome_1|MORM_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_and_related_disorders|not_provided": 1,
    "INPP5E-related_disorder|Inborn_genetic_diseases|Joubert_syndrome_1|MORM_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|not_specified|not_provided|INPP5E-related_disorder|Joubert_syndrome_1|MORM_syndrome": 1,
    "not_specified|INPP5E-related_disorder|Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome": 1,
    "Joubert_syndrome|INPP5E-related_disorder|Joubert_syndrome_1|MORM_syndrome|not_provided": 1,
    "not_specified|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_1|not_specified|not_provided|Joubert_syndrome": 1,
    "INPP5E-related_disorder|Joubert_syndrome_1|MORM_syndrome|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_1|Joubert_syndrome|Retinal_dystrophy|not_specified|MORM_syndrome": 1,
    "Joubert_syndrome_1|MORM_syndrome|Joubert_syndrome|INPP5E-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|INPP5E-related_disorder|Joubert_syndrome": 4,
    "not_provided|Retinal_dystrophy|MORM_syndrome|Joubert_syndrome_1|not_specified|Rod-cone_dystrophy|Inborn_genetic_diseases|INPP5E-related_disorder|Joubert_syndrome": 1,
    "MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome|INPP5E-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Joubert_syndrome_1|not_provided|Joubert_syndrome|INPP5E-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|INPP5E-related_disorder|not_provided|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome|INPP5E-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome": 4,
    "MORM_syndrome|Joubert_syndrome_1|Inborn_genetic_diseases|Joubert_syndrome|INPP5E-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|INPP5E-related_disorder|MORM_syndrome|Joubert_syndrome_1|Joubert_syndrome": 1,
    "Joubert_syndrome_1|not_provided|not_specified|Joubert_syndrome": 1,
    "Joubert_syndrome_1|Inborn_genetic_diseases|INPP5E-related_disorder|Joubert_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome|Rod-cone_dystrophy": 1,
    "INPP5E-related_disorder|Retinal_dystrophy|not_provided|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_1|MORM_syndrome|not_provided|Joubert_syndrome|INPP5E-related_disorder|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|INPP5E-related_disorder|not_provided|Joubert_syndrome|Joubert_syndrome_1|MORM_syndrome": 1,
    "Joubert_syndrome_1|MORM_syndrome|Inborn_genetic_diseases|Joubert_syndrome|INPP5E-related_disorder": 1,
    "Joubert_syndrome|INPP5E-related_disorder|MORM_syndrome|Joubert_syndrome_1": 1,
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    "INPP5E-related_disorder|Joubert_syndrome|not_provided|Joubert_syndrome_1": 1,
    "not_specified|INPP5E-related_disorder|Joubert_syndrome_1|not_provided": 1,
    "INPP5E-related_disorder|Joubert_syndrome_1": 1,
    "NOTCH1-related_disorder|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified": 5,
    "Adams-Oliver_syndrome_5": 1386,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Adams-Oliver_syndrome_5": 8,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|Pulmonary_arterial_hypertension|NOTCH1-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified": 2,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 16,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 246,
    "Adams-Oliver_syndrome_5|not_specified": 35,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 252,
    "NOTCH1-related_disorder|not_specified|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "not_specified|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 14,
    "not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 11,
    "not_specified|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "NOTCH1-related_disorder": 40,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Adams-Oliver_syndrome_5": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 8,
    "NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5": 2,
    "not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 20,
    "Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5": 27,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 11,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|not_specified": 2,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 2,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|not_specified|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 23,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1": 12,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided": 8,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified": 5,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 24,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|not_specified": 1,
    "not_specified|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 10,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Cardiovascular_phenotype": 1,
    "NOTCH1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 3,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 34,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 2,
    "Adams-Oliver_syndrome_5|not_provided": 70,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided|not_specified|Aortic_valve_disease_1": 3,
    "not_provided|Adams-Oliver_syndrome_5": 64,
    "Adams-Oliver_syndrome_5|Connective_tissue_disorder": 3,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Connective_tissue_disorder": 1,
    "Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 4,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 15,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 20,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|Hypoplastic_left_heart_syndrome": 1,
    "Aortic_valve_disease_1|not_provided|Adams-Oliver_syndrome_5": 8,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5": 7,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 1,
    "not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 6,
    "not_specified|Adams-Oliver_syndrome_5": 21,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 5,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 3,
    "not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 4,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 14,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 11,
    "not_provided|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "not_provided|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Hypoplastic_left_heart_syndrome|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 9,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided|NOTCH1-related_disorder": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1": 2,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Connective_tissue_disorder": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided": 10,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided": 8,
    "not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "not_provided|Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_specified": 1,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 1,
    "Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1": 14,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 1,
    "not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 1,
    "not_provided|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 8,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 5,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Connective_tissue_disorder|not_specified": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1": 2,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided": 8,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1": 4,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "not_specified|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Aortic_valve_disorder|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided": 16,
    "Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Adams-Oliver_syndrome_5": 2,
    "not_provided|Aortic_valve_disease_1|NOTCH1-related_disorder|Connective_tissue_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|NOTCH1-related_disorder|not_provided": 1,
    "NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Adams-Oliver_syndrome_5|Adams-Oliver_syndrome|Aortic_valve_disorder": 1,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 5,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 7,
    "not_specified|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided": 1,
    "not_specified|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_provided": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 2,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 13,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Marfan_syndrome|Aortic_valve_disease_1|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 2,
    "Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5": 3,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|NOTCH1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 9,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|not_specified|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided": 1,
    "not_specified|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "not_provided|not_specified|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 1,
    "not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 5,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|NOTCH1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_provided": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Aortic_valve_disease_1|KA-like_vemurafenib-induced_squamous_lesions|NOTCH1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 2,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|NOTCH1-related_disorder": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided": 5,
    "not_specified|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 12,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided|Adams-Oliver_syndrome_5": 5,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder": 9,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 7,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 1,
    "not_specified|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|not_specified": 3,
    "Aortic_valve_disease_1|not_specified|not_provided|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1|not_specified": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Connective_tissue_disorder": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 2,
    "NOTCH1-related_disorder|not_provided|Pulmonary_arterial_hypertension|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 1,
    "not_specified|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 2,
    "Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1": 11,
    "NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|NOTCH1-related_disorder": 1,
    "not_specified|not_provided|Bicuspid_aortic_valve|Narrow_palate|Abnormal_vena_cava_morphology|Aortic_tortuosity|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Adams-Oliver_syndrome_5|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 6,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 4,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided": 1,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 13,
    "not_specified|Connective_tissue_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Aortic_valve_disease_1": 1,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_provided|not_specified": 1,
    "Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 1,
    "Adams-Oliver_syndrome_5|not_provided|Shone_complex|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1": 3,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|not_provided|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Aortic_valve_disease_1": 1,
    "not_provided|Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Adams-Oliver_syndrome_5": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified|NOTCH1-related_disorder|not_provided": 1,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Aortic_valve_disease_1|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|not_provided": 1,
    "not_provided|Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1": 2,
    "NOTCH1-related_disorder|Connective_tissue_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 3,
    "Cholesteatoma_of_middle_ear|Adams-Oliver_syndrome_5": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided|NOTCH1-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Benign_hereditary_chorea|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|not_provided": 1,
    "not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Aortic_valve_disease_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heart|_malformation_of": 1,
    "not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Myeloproliferative_neoplasm|_unclassifiable|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|not_specified": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 2,
    "NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_specified": 1,
    "NOTCH1-related_disorder|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 4,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided": 3,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Connective_tissue_disorder|Aortic_valve_disease_1": 2,
    "not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Marfan_syndrome|Aortic_valve_disease_1": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hypoplastic_left_heart_syndrome|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided": 1,
    "Hypoplastic_left_heart_syndrome|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|NOTCH1-related_disorder|not_provided|Neurofibromatosis|_type_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|NOTCH1-related_disorder": 1,
    "Aortic_valve_disease_1|not_provided|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_specified|not_provided": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1": 2,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Connective_tissue_disorder|not_provided": 1,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|NOTCH1-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Adams-Oliver_syndrome_5|not_specified": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_valve_disease_1|not_provided": 1,
    "NOTCH1-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 2,
    "not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Aortic_valve_disease_1|not_provided": 1,
    "not_provided|NOTCH1-related_disorder": 1,
    "Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1|Cataract": 1,
    "Adams-Oliver_syndrome_5|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|not_specified|not_provided|Connective_tissue_disorder|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1|not_provided": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|not_specified": 1,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Adams-Oliver_syndrome_5|not_specified|not_provided|Aortic_valve_disease_1": 2,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 2,
    "not_specified|NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided": 1,
    "not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 1,
    "not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Connective_tissue_disorder|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified|not_provided|NOTCH1-related_disorder|Connective_tissue_disorder": 1,
    "not_specified|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|NOTCH1-related_disorder": 4,
    "Adams-Oliver_syndrome_5|Thoracic_aortic_aneurysm": 1,
    "not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|not_provided": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disorder": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 1,
    "NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Connective_tissue_disorder|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|not_specified": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|not_provided": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1": 2,
    "not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Congenital_heart_disease|Aortic_valve_disorder|NOTCH1-related_disorder|not_specified|not_provided": 1,
    "Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Arterial_dissection": 1,
    "not_specified|Adams-Oliver_syndrome_5|not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 1,
    "not_provided|Adams-Oliver_syndrome_5|Pulmonary_arterial_hypertension": 1,
    "Aortic_valve_disease_1|Chronic_adenoiditis|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|not_provided|Anophthalmia-microphthalmia_syndrome|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided": 1,
    "not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "not_provided|Adams-Oliver_syndrome_5|NOTCH1-related_disorder": 1,
    "Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided": 1,
    "not_provided|Adams-Oliver_syndrome_5|Myeloproliferative_neoplasm|_unclassifiable|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_heart_anomalies|Adams-Oliver_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 2,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 3,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_specified|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1": 1,
    "not_specified|not_provided|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 1,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|not_provided|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|NOTCH1-related_disorder|Connective_tissue_disorder|Aortic_valve_disease_1": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified": 1,
    "not_specified|not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 1,
    "Aortic_valve_disease_1|Pulmonary_arterial_hypertension|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_2|Aortic_valve_disorder|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided|not_specified": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified": 1,
    "Adams-Oliver_syndrome_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Aortic_valve_disease_1": 2,
    "not_provided|not_specified|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified|Connective_tissue_disorder": 1,
    "not_provided|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_specified": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|not_provided|Aortic_valve_disease_1": 1,
    "not_specified|Aortic_valve_disease_1|Connective_tissue_disorder|Adams-Oliver_syndrome_5": 1,
    "not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified": 2,
    "Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_specified|not_provided": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|not_provided|NOTCH1-related_disorder|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|not_specified|Aortic_valve_disease_1": 1,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|Aortic_valve_disease_1|not_provided|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_provided|Adams-Oliver_syndrome_5|Aortic_valve_disease_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_specified|not_provided|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1|Cholesteatoma_of_middle_ear|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided": 1,
    "not_provided|Aortic_valve_disease_1|not_specified|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Aortic_valve_disease_1": 1,
    "Aortic_valve_disease_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|NOTCH1-related_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5": 1,
    "NOTCH1-related_disorder|Connective_tissue_disorder|Adams-Oliver_syndrome_5": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|not_provided|not_specified|NOTCH1-related_disorder": 1,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_valve_disease_1|not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|not_specified|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 1,
    "not_specified|Aortic_valve_disease_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Connective_tissue_disorder|not_specified|Adams-Oliver_syndrome_5": 1,
    "Adams-Oliver_syndrome_5|Ehlers-Danlos_syndrome|_type_3": 1,
    "Adams-Oliver_syndrome_5|Aortic_valve_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided": 4,
    "Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Adams-Oliver_syndrome_5|not_specified|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Adams-Oliver_syndrome_5": 1,
    "not_provided|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Pulmonary_arterial_hypertension|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Adams-Oliver_syndrome_5|not_provided|Aortic_valve_disease_1|Cholesteatoma_of_middle_ear": 1,
    "not_provided|NOTCH1-related_disorder|Adams-Oliver_syndrome_5": 1,
    "Aortic_valve_disease_1|NOTCH1-related_disorder|Adams-Oliver_syndrome_5|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_valve_disease_1|Adams-Oliver_syndrome_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "NOTCH1-related_disorder|Connective_tissue_disorder|Adams-Oliver_syndrome_5|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_valve_disease_1": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder|Aortic_valve_disease_1|Adams-Oliver_syndrome_5": 1,
    "NOTCH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Adams-Oliver_syndrome_5|Connective_tissue_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_valve_disease_1": 1,
    "not_provided|Inborn_genetic_diseases|Adams-Oliver_syndrome_5": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NOTCH1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Adams-Oliver_syndrome_5|NOTCH1-related_disorder|Myeloproliferative_neoplasm|_unclassifiable|Aortic_valve_disease_1": 1,
    "Adams-Oliver_syndrome_5|not_specified|NOTCH1-related_disorder": 1,
    "NOTCH1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Congenital_generalized_lipodystrophy_type_1": 103,
    "Congenital_generalized_lipodystrophy_type_1|not_provided": 26,
    "not_provided|Congenital_generalized_lipodystrophy_type_1": 11,
    "Congenital_generalized_lipodystrophy|not_provided": 2,
    "Monogenic_diabetes|Congenital_generalized_lipodystrophy_type_1|not_provided": 1,
    "Congenital_generalized_lipodystrophy_type_1|Inborn_genetic_diseases": 5,
    "not_provided|Congenital_generalized_lipodystrophy_type_1|AGPAT2-related_disorder": 2,
    "Inborn_genetic_diseases|Congenital_generalized_lipodystrophy_type_1": 4,
    "Inborn_genetic_diseases|Congenital_generalized_lipodystrophy_type_1|not_provided": 1,
    "Congenital_generalized_lipodystrophy_type_1|AGPAT2-related_disorder|not_provided": 2,
    "Congenital_generalized_lipodystrophy_type_1|AGPAT2-related_disorder": 1,
    "not_specified|Congenital_generalized_lipodystrophy_type_1|not_provided": 3,
    "AGPAT2-related_disorder|not_provided": 1,
    "not_provided|Congenital_generalized_lipodystrophy_type_1|AGPAT2-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy_type_1|Monogenic_diabetes|not_provided": 1,
    "Congenital_generalized_lipodystrophy|not_provided|Congenital_generalized_lipodystrophy_type_1": 1,
    "Congenital_generalized_lipodystrophy_type_1|Congenital_generalized_lipodystrophy": 1,
    "not_provided|not_specified|Congenital_generalized_lipodystrophy_type_1": 1,
    "Monogenic_diabetes|AGPAT2-related_disorder|not_specified|not_provided|Congenital_generalized_lipodystrophy_type_1": 1,
    "Monogenic_diabetes|Congenital_generalized_lipodystrophy_type_1|not_provided|Inborn_genetic_diseases": 2,
    "Monogenic_diabetes|Congenital_generalized_lipodystrophy_type_1|Inborn_genetic_diseases": 1,
    "AGPAT2-related_disorder|not_provided|Congenital_generalized_lipodystrophy_type_1|Monogenic_diabetes|not_specified": 1,
    "not_provided|Congenital_generalized_lipodystrophy_type_1|not_specified": 1,
    "AGPAT2-related_disorder|not_provided|Congenital_generalized_lipodystrophy_type_1|Monogenic_diabetes": 1,
    "Congenital_generalized_lipodystrophy": 3,
    "Congenital_generalized_lipodystrophy_type_1|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_generalized_lipodystrophy_type_1": 1,
    "Monogenic_diabetes|not_provided|Congenital_generalized_lipodystrophy_type_1": 2,
    "Congenital_generalized_lipodystrophy_type_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_generalized_lipodystrophy_type_1|not_specified|not_provided": 1,
    "Congenital_generalized_lipodystrophy_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy|not_specified|not_provided": 1,
    "C8G-related_disorder": 10,
    "C8G-related_disorder|Immunodeficiency": 1,
    "not_specified|Immunodeficiency": 26,
    "C8G-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_with_poor_growth_and_with_or_without_seizures_or_ataxia|not_provided": 15,
    "ABCA2-related_disorder": 36,
    "not_specified|ABCA2-related_disorder": 2,
    "Intellectual_developmental_disorder_with_poor_growth_and_with_or_without_seizures_or_ataxia": 28,
    "not_provided|Intellectual_developmental_disorder_with_poor_growth_and_with_or_without_seizures_or_ataxia": 2,
    "not_provided|ABCA2-related_disorder": 6,
    "not_specified|Intellectual_developmental_disorder_with_poor_growth_and_with_or_without_seizures_or_ataxia": 6,
    "ABCA2-related_disorder|not_specified|not_provided": 1,
    "Intellectual_developmental_disorder_with_poor_growth_and_with_or_without_seizures_or_ataxia|not_specified": 4,
    "not_provided|Ataxia_with_Dysarthria": 1,
    "ABCA2-related_disorder|not_provided": 5,
    "ABCA2-related_disorder|not_specified": 2,
    "ABCA2-related_disorder|Intellectual_developmental_disorder_with_poor_growth_and_with_or_without_seizures_or_ataxia": 1,
    "Rafiq_syndrome|Inborn_genetic_diseases": 24,
    "Rafiq_syndrome": 288,
    "Inborn_genetic_diseases|Rafiq_syndrome": 25,
    "Inborn_genetic_diseases|Rafiq_syndrome|MAN1B1-related_disorder|Intellectual_disability": 1,
    "MAN1B1-related_disorder|not_provided|Rafiq_syndrome": 1,
    "not_specified|not_provided|Rafiq_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Rafiq_syndrome|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|Rafiq_syndrome|not_specified": 1,
    "Rafiq_syndrome|MAN1B1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Rafiq_syndrome": 3,
    "not_specified|MAN1B1-related_disorder|Inborn_genetic_diseases|Rafiq_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|MAN1B1-related_disorder|Rafiq_syndrome": 1,
    "MAN1B1-congenital_disorder_of_glycosylation|Rafiq_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Rafiq_syndrome": 6,
    "not_specified|Rafiq_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "MAN1B1-related_disorder|Rafiq_syndrome": 3,
    "MAN1B1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rafiq_syndrome": 2,
    "MAN1B1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Rafiq_syndrome": 6,
    "Inborn_genetic_diseases|not_provided|MAN1B1-related_disorder|Rafiq_syndrome|not_specified": 1,
    "Rafiq_syndrome|not_provided": 11,
    "not_provided|Rafiq_syndrome|Inborn_genetic_diseases": 3,
    "MAN1B1-related_disorder": 2,
    "Intellectual_disability|not_specified|Rafiq_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Rafiq_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|MAN1B1-related_disorder|not_provided|Rafiq_syndrome|See_cases": 1,
    "Inborn_genetic_diseases|not_specified|Rafiq_syndrome": 4,
    "not_provided|Inborn_genetic_diseases|Rafiq_syndrome|not_specified": 1,
    "not_specified|Rafiq_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Rafiq_syndrome": 4,
    "not_specified|Inborn_genetic_diseases|Rafiq_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|MAN1B1-related_disorder|not_specified|not_provided|Rafiq_syndrome": 1,
    "Inborn_genetic_diseases|MAN1B1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Rafiq_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Rafiq_syndrome": 1,
    "Rafiq_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|MAN1B1-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Rafiq_syndrome": 1,
    "Rafiq_syndrome|not_specified|not_provided": 1,
    "Rafiq_syndrome|not_specified": 1,
    "Rafiq_syndrome|MAN1B1-related_disorder": 1,
    "Inborn_genetic_diseases|MAN1B1-related_disorder|Rafiq_syndrome": 1,
    "not_provided|MAN1B1-related_disorder|Rafiq_syndrome|Inborn_genetic_diseases": 1,
    "Rafiq_syndrome|MAN1B1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Rafiq_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Rafiq_syndrome|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 703,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases": 16,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Intellectual_disability": 3,
    "not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 26,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 42,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 19,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 4,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided": 54,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_specified": 3,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_specified": 11,
    "GRIN1-related_disorder|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 2,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided|not_specified": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Developmental_and_epileptic_encephalopathy_101": 1,
    "Developmental_and_epileptic_encephalopathy_101": 3,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|GRIN1-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 3,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided": 2,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases|not_specified": 2,
    "GRIN1-related_disorder|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 2,
    "GRIN1-related_disorder": 3,
    "NEURODEVELOPMENTAL_DISORDER_WITH_HYPERKINETIC_MOVEMENTS_WITH_OR_WITHOUT_SEIZURES|_AUTOSOMAL_RECESSIVE|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_HYPERKINETIC_MOVEMENTS_WITH_OR_WITHOUT_SEIZURES|_AUTOSOMAL_RECESSIVE|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 4,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases|not_provided|GRIN1-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Developmental_and_epileptic_encephalopathy_101|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Inborn_genetic_diseases|not_specified|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Inborn_genetic_diseases|not_provided|not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Developmental_and_epileptic_encephalopathy_101|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Intellectual_disability|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 3,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "GRIN1-related_disorder|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|not_specified": 1,
    "not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy_101|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 1,
    "Autism_spectrum_disorder|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "GRIN1-related_disorder|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided": 1,
    "not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive": 2,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Seizure": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Developmental_and_epileptic_encephalopathy_101": 1,
    "GRIN1-related_disorder|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Developmental_and_epileptic_encephalopathy_101": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Developmental_and_epileptic_encephalopathy|_1": 1,
    "GRIN1-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Developmental_and_epileptic_encephalopathy_101|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided|not_specified": 1,
    "not_provided|GRIN1-related_disorder|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|GRIN1-related_disorder|not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_HYPERKINETIC_MOVEMENTS_AND_WITH_OR_WITHOUT_SEIZURES|_AUTOSOMAL_DOMINANT|not_provided|Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_specified|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_recessive|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_hyperkinetic_movements_and_seizures|_autosomal_dominant|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|not_specified|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_79|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|not_specified": 1,
    "not_provided|not_specified|TPRN-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79": 12,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|Inborn_genetic_diseases": 1,
    "not_provided|TPRN-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_79": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_79": 1,
    "TPRN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_79": 2,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_79": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_79|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_79": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|not_provided|not_specified": 1,
    "Ear_malformation|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_79|TPRN-related_disorder|Rare_genetic_deafness|not_provided": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_provided": 50,
    "SLC34A3-related_disorder": 25,
    "SLC34A3-related_disorder|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease": 6,
    "Autosomal_recessive_hypophosphatemic_bone_disease": 116,
    "not_provided|Autosomal_recessive_hypophosphatemic_bone_disease": 64,
    "Autosomal_recessive_hypophosphatemic_bone_disease|Inborn_genetic_diseases": 14,
    "not_provided|not_specified|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease": 5,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_provided|Inborn_genetic_diseases": 5,
    "not_specified|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease": 6,
    "not_provided|SLC34A3-related_disorder": 10,
    "not_provided|Autosomal_recessive_hypophosphatemic_bone_disease|SLC34A3-related_disorder": 2,
    "Autosomal_recessive_hypophosphatemic_bone_disease|Inborn_genetic_diseases|not_provided": 1,
    "SLC34A3-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|Autosomal_recessive_hypophosphatemic_bone_disease|not_provided": 6,
    "not_provided|not_specified|SLC34A3-related_disorder|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "not_specified|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease|Kidney_disorder": 2,
    "not_provided|not_specified|SLC34A3-related_disorder": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_1": 1,
    "Hypercalciuria": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_provided|not_specified": 3,
    "not_provided|SLC34A3-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|SLC34A3-related_disorder|not_provided": 1,
    "not_provided|SLC34A3-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_provided|not_specified|SLC34A3-related_disorder": 2,
    "SLC34A3-related_disorder|not_specified|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease": 3,
    "SLC34A3-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|SLC34A3-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease|not_specified": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|SLC34A3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_hypophosphatemic_bone_disease|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_hypophosphatemic_bone_disease": 2,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_hypophosphatemic_bone_disease": 5,
    "not_provided|Autosomal_recessive_hypophosphatemic_bone_disease|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_hypophosphatemic_bone_disease|Hypercalciuria|not_provided": 1,
    "not_provided|SLC34A3-related_disorder|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "SLC34A3-related_disorder|Autosomal_recessive_hypophosphatemic_bone_disease|not_provided": 1,
    "SLC34A3-related_disorder|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|not_provided|SLC34A3-related_disorder": 1,
    "not_provided|not_specified|Autosomal_recessive_hypophosphatemic_bone_disease|SLC34A3-related_disorder": 1,
    "not_specified|not_provided|SLC34A3-related_disorder|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "SLC34A3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "SLC34A3-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_hypophosphatemic_bone_disease": 1,
    "Autosomal_recessive_hypophosphatemic_bone_disease|Nephrolithiasis/nephrocalcinosis": 1,
    "TUBB4B-related_disorder": 9,
    "not_provided|TUBB4B-related_disorder": 5,
    "TUBB4B-related_disorder|not_provided": 7,
    "Leber_congenital_amaurosis_with_early-onset_deafness": 4,
    "not_provided|Leber_congenital_amaurosis_with_early-onset_deafness": 1,
    "Leber_congenital_amaurosis_with_early-onset_deafness|not_provided": 2,
    "Hypogonadotropic_hypogonadism_9_with_or_without_anosmia": 10,
    "not_provided|NSMF-related_disorder": 4,
    "NSMF-related_disorder|not_provided": 3,
    "not_provided|Hypogonadotropic_hypogonadism_9_with_or_without_anosmia": 1,
    "NSMF-related_disorder": 6,
    "not_provided|NSMF-related_disorder|not_specified|Hypogonadotropic_hypogonadism_9_with_or_without_anosmia": 1,
    "PNPLA7-related_condition": 2,
    "Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development|not_specified": 1,
    "Mulibrey_nanism_syndrome": 107,
    "not_provided|Kleefstra_syndrome_1": 87,
    "not_provided|not_specified|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|not_provided": 74,
    "Inborn_genetic_diseases|EHMT1-related_disorder|not_specified|not_provided|Kleefstra_syndrome_1": 4,
    "Kleefstra_syndrome_1|Inborn_genetic_diseases": 60,
    "Neurodevelopmental_disorder|not_provided|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1": 56,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|not_specified|not_provided|See_cases": 1,
    "Kleefstra_syndrome_1|EHMT1-related_disorder": 10,
    "EHMT1-related_disorder|Kleefstra_syndrome_1|not_specified": 1,
    "not_specified|Kleefstra_syndrome_1": 16,
    "not_provided|Inborn_genetic_diseases|Kleefstra_syndrome_1": 7,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|not_provided": 19,
    "Inborn_genetic_diseases|not_provided|Kleefstra_syndrome_1": 22,
    "EHMT1-related_disorder|Kleefstra_syndrome_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Kleefstra_syndrome_1": 3,
    "not_specified|Kleefstra_syndrome_1|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Kleefstra_syndrome_1": 12,
    "not_provided|EHMT1-related_disorder|Kleefstra_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|not_specified|not_provided": 1,
    "Kleefstra_syndrome_1|not_specified": 14,
    "not_specified|Kleefstra_syndrome_1|not_provided": 4,
    "EHMT1-related_disorder|Kleefstra_syndrome_1": 9,
    "Kleefstra_syndrome_1|Inborn_genetic_diseases|not_provided": 7,
    "not_provided|Kleefstra_syndrome_1|Inborn_genetic_diseases": 8,
    "not_specified|not_provided|Inborn_genetic_diseases|Kleefstra_syndrome_1": 2,
    "EHMT1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Kleefstra_syndrome_1": 4,
    "not_provided|Kleefstra_syndrome_1|EHMT1-related_disorder|Inborn_genetic_diseases": 2,
    "EHMT1-related_disorder|Inborn_genetic_diseases|not_provided|Kleefstra_syndrome_1": 4,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|EHMT1-related_disorder|not_specified|not_provided": 1,
    "EHMT1-related_disorder|Inborn_genetic_diseases|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|Intellectual_disability": 1,
    "not_provided|Kleefstra_syndrome_1|not_specified": 5,
    "Intellectual_disability|Kleefstra_syndrome_1": 1,
    "Inborn_genetic_diseases|not_specified|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Epilepsy|Kleefstra_syndrome_1": 1,
    "not_provided|Kleefstra_syndrome_1|Inborn_genetic_diseases|EHMT1-related_disorder": 2,
    "EHMT1-related_disorder": 11,
    "Kleefstra_syndrome_1|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|EHMT1-related_disorder|not_provided|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Kleefstra_syndrome_1|not_provided|Inborn_genetic_diseases": 8,
    "Kleefstra_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|EHMT1-related_disorder|Kleefstra_syndrome_1": 1,
    "not_specified|Inborn_genetic_diseases|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome|Kleefstra_syndrome_1": 1,
    "not_provided|Kleefstra_syndrome": 1,
    "not_provided|Kleefstra_syndrome_1|EHMT1-related_disorder": 3,
    "not_specified|Inborn_genetic_diseases|Kleefstra_syndrome_1|not_provided": 1,
    "Kleefstra_syndrome_1|Kleefstra_syndrome": 1,
    "not_provided|not_specified|Kleefstra_syndrome_1|Inborn_genetic_diseases": 2,
    "Kleefstra_syndrome_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Kleefstra_syndrome_1|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Kleefstra_syndrome_1|Intellectual_disability": 1,
    "EHMT1-related_disorder|not_provided|Inborn_genetic_diseases|Intellectual_disability|Kleefstra_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Kleefstra_syndrome_1|EHMT1-related_disorder": 2,
    "EHMT1-related_disorder|Kleefstra_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Kleefstra_syndrome_1|EHMT1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "EHMT1-related_disorder|not_specified|not_provided|Kleefstra_syndrome_1": 3,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|Kleefstra_syndrome_1": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|Marfanoid_habitus_and_intellectual_disability|not_provided": 1,
    "not_specified|Kleefstra_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Synophrys|Schizophrenia|Anteverted_nares|Coarse_facial_features|Intellectual_disability|Kleefstra_syndrome_1": 1,
    "EHMT1-related_disorder|not_provided|Kleefstra_syndrome_1": 2,
    "not_provided|Inborn_genetic_diseases|EHMT1-related_disorder|Kleefstra_syndrome_1": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|not_provided|EHMT1-related_disorder": 1,
    "EHMT1-related_disorder|not_provided": 2,
    "not_provided|EHMT1-related_disorder": 1,
    "Kleefstra_syndrome_1|not_provided|EHMT1-related_disorder": 2,
    "not_provided|Global_developmental_delay|Difficulty_walking|Abnormal_facial_shape|Polymicrogyria|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_provided|Kleefstra_syndrome_1|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|not_provided|not_specified": 1,
    "not_specified|Kleefstra_syndrome_1|Inborn_genetic_diseases": 1,
    "Kleefstra_syndrome_1|Inborn_genetic_diseases|EHMT1-related_disorder": 1,
    "not_provided|EHMT1-related_disorder|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|Autism_spectrum_disorder": 1,
    "EHMT1-related_disorder|not_provided|Inborn_genetic_diseases|Kleefstra_syndrome_1": 1,
    "Kleefstra_syndrome_1|See_cases": 1,
    "Inborn_genetic_diseases|EHMT1-related_disorder": 1,
    "Inborn_genetic_diseases|Kleefstra_syndrome_1|not_specified": 1,
    "CACNA1B-related_disorder": 15,
    "CACNA1B-related_disorder|not_provided": 21,
    "not_provided|CACNA1B-related_disorder": 6,
    "Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|not_provided": 14,
    "Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements": 35,
    "not_provided|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements": 11,
    "not_specified|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|not_provided": 1,
    "not_specified|not_provided|CACNA1B-related_disorder": 1,
    "not_provided|not_specified|Dystonia_23": 1,
    "Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|CACNA1B-related_disorder|not_provided": 1,
    "CACNA1B-related_disorder|not_specified|not_provided": 2,
    "CACNA1B-related_disorder|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|not_provided": 1,
    "Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|not_provided|not_specified": 3,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements": 1,
    "Dystonia_23|not_provided": 1,
    "Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|not_specified|not_provided": 5,
    "CACNA1B-related_neurodevelopmental_disorder": 1,
    "Complex_neurodevelopmental_disorder_with_motor_features|not_provided": 1,
    "not_provided|not_specified|CACNA1B-related_disorder": 1,
    "not_specified|not_provided|CACNA1B-related_disorder|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements": 1,
    "not_specified|CACNA1B-related_disorder|not_provided": 2,
    "not_specified|Complex_neurodevelopmental_disorder_with_motor_features|CACNA1B-related_disorder|not_provided": 1,
    "CACNA1B-related_disorder|not_specified|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements|not_provided": 1,
    "CACNA1B-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|Neurodevelopmental_disorder_with_seizures_and_nonepileptic_hyperkinetic_movements": 1,
    "not_provided|Dystonia_23|CACNA1B-related_disorder": 1,
    "Oocyte_maturation_defect_2": 48,
    "not_provided|Oocyte_maturation_defect_2": 12,
    "not_specified|Oocyte_maturation_defect_2": 1,
    "Oocyte_maturation_defect_2|not_specified": 1,
    "Inherited_oocyte_maturation_defect|Oocyte_maturation_defect_2": 1,
    "Female_infertility": 2,
    "Oocyte_maturation_defect_2|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_30": 51,
    "Intellectual_disability|_autosomal_dominant_30|not_provided": 11,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_30": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_30|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_30": 7,
    "ZMYND11-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_30": 2,
    "ZMYND11-related_disorder": 6,
    "not_provided|Intellectual_disability|_autosomal_dominant_30|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_30|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_30|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_30|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_30|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_30|Decreased_body_weight|Absent_speech|Chronic_constipation|Self-mutilation|Motor_delay|Self-injurious_behavior": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_30|not_provided": 1,
    "ZMYND11-related_neurodevelopmental_disorder_with_multiple_anomalies": 1,
    "ZMYND11-related_disorder|Neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_30|Inborn_genetic_diseases|not_provided|Global_developmental_delay": 1,
    "DIP2C-related_disorder|not_provided": 9,
    "not_provided|DIP2C-associated_disorder": 1,
    "not_provided|DIP2C-related_disorder": 17,
    "DIP2C-related_disorder": 10,
    "Inborn_genetic_diseases|not_provided|DIP2C-related_disorder": 1,
    "DIP2C-related_neurodevelopmental_disorder": 1,
    "Neurodevelopmental_delay|Obesity": 1,
    "WDR37-related_disorder": 13,
    "WDR37-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Neurooculocardiogenitourinary_syndrome": 14,
    "WDR37-related_disorder|not_provided": 1,
    "not_provided|Neurooculocardiogenitourinary_syndrome": 1,
    "Epilepsy|Dysmorphism|Congenital_cerebellar_hypoplasia|Congenital_ocular_coloboma|Intellectual_disability|Developmental_delay|Neurooculocardiogenitourinary_syndrome": 1,
    "not_provided|WDR37-related_disorder": 2,
    "Congenital_cerebellar_hypoplasia|Developmental_delay|Intellectual_disability|Dysmorphism|Epilepsy|Congenital_ocular_coloboma|Neurooculocardiogenitourinary_syndrome|WDR37-related_disorder|not_provided|Cerebellar_vermis_hypoplasia|Ventriculomegaly": 1,
    "Neurooculocardiogenitourinary_syndrome|Dysmorphism|Congenital_cerebellar_hypoplasia|Epilepsy|Congenital_ocular_coloboma|Intellectual_disability|Developmental_delay": 1,
    "Neurooculocardiogenitourinary_syndrome|Inborn_genetic_diseases|Dysmorphism|Intellectual_disability|Developmental_delay|Congenital_cerebellar_hypoplasia|Epilepsy|Congenital_ocular_coloboma": 1,
    "Neurooculocardiogenitourinary_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|WDR37-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Neurooculocardiogenitourinary_syndrome": 2,
    "See_cases|WDR37-related_disorder": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Neurooculocardiogenitourinary_syndrome": 1,
    "PFKP-related_disorder": 4,
    "not_provided|PITRM1-related_disorder": 14,
    "PITRM1-related_disorder|not_provided": 14,
    "Spinocerebellar_ataxia|_autosomal_recessive_30": 3,
    "PITRM1-related_disorder": 4,
    "Infantile_onset_spinocerebellar_ataxia": 11,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_30": 1,
    "not_provided|PITRM1-related_disorder|not_specified": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_30|not_provided": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_30|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Prostate_cancer|_somatic": 10,
    "46|XY_disorder_of_sex_development_due_to_testicular_17|20-desmolase_deficiency": 8,
    "AKR1C2-related_disorder": 8,
    "CIC-rearranged_sarcoma|not_specified|46|XY_disorder_of_sex_development_due_to_testicular_17|20-desmolase_deficiency|AKR1C2-related_disorder": 1,
    "AKR1C2-related_disorder|not_specified|not_provided|46|XY_disorder_of_sex_development_due_to_testicular_17|20-desmolase_deficiency": 1,
    "AKR1C2-related_disorder|not_provided": 1,
    "46|XY_disorder_of_sex_development_due_to_testicular_17|20-desmolase_deficiency|not_specified": 1,
    "AKR1C4-related_disorder": 16,
    "AKR1C4-related_disorder|not_provided": 4,
    "not_specified|AKR1C4-related_disorder": 4,
    "not_provided|AKR1C4-related_disorder": 5,
    "AKR1C4-related_disorder|not_specified": 2,
    "not_specified|AKR1C4-related_disorder|not_provided": 2,
    "Immunodeficiency_due_to_CD25_deficiency|not_provided": 11,
    "Immunodeficiency_due_to_CD25_deficiency": 241,
    "not_provided|Immunodeficiency_due_to_CD25_deficiency": 18,
    "not_specified|Immunodeficiency_due_to_CD25_deficiency": 14,
    "Immunodeficiency_due_to_CD25_deficiency|not_provided|Pleural_effusion|Myelodysplasia": 1,
    "not_specified|Immunodeficiency_due_to_CD25_deficiency|not_provided": 2,
    "Immunodeficiency_due_to_CD25_deficiency|Type_1_diabetes_mellitus_10|not_provided|not_specified": 1,
    "Immunodeficiency_due_to_CD25_deficiency|not_specified": 9,
    "IL2RA-related_disorder|Immunodeficiency_due_to_CD25_deficiency": 2,
    "Immunodeficiency_due_to_CD25_deficiency|Type_1_diabetes_mellitus_10": 2,
    "not_provided|Immunodeficiency_due_to_CD25_deficiency|not_specified": 1,
    "Type_1_diabetes_mellitus_10|Immunodeficiency_due_to_CD25_deficiency": 2,
    "Immunodeficiency_due_to_CD25_deficiency|not_specified|not_provided": 2,
    "not_specified|not_provided|Immunodeficiency_due_to_CD25_deficiency": 1,
    "Immunodeficiency_due_to_CD25_deficiency|not_provided|not_specified": 1,
    "not_provided|IL2RA-related_disorder|Immunodeficiency_due_to_CD25_deficiency": 1,
    "not_provided|not_specified|Immunodeficiency_due_to_CD25_deficiency": 1,
    "IL2RA-related_disorder|Type_1_diabetes_mellitus_10": 2,
    "Inflammatory_bowel_disease_1|not_provided": 1,
    "Hypoparathyroidism|_deafness|_renal_disease_syndrome": 127,
    "Hypoparathyroidism|_deafness|_renal_disease_syndrome|not_provided": 21,
    "not_provided|Hypoparathyroidism|_deafness|_renal_disease_syndrome": 36,
    "not_specified|not_provided|Hypoparathyroidism|_deafness|_renal_disease_syndrome": 5,
    "GATA3-related_disorder|not_provided": 2,
    "GATA3-related_disorder|not_provided|Hypoparathyroidism|_deafness|_renal_disease_syndrome": 3,
    "Hypoparathyroidism|_deafness|_renal_disease_syndrome|GATA3-related_disorder|not_provided": 2,
    "GATA3-related_disorder": 9,
    "Hypoparathyroidism|_deafness|_renal_disease_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypoparathyroidism|_deafness|_renal_disease_syndrome|GATA3-related_disorder|not_specified": 1,
    "GATA3-related_disorder|Hypoparathyroidism|_deafness|_renal_disease_syndrome": 2,
    "Hypoparathyroidism|_deafness|_renal_disease_syndrome|not_provided|Hearing_impairment": 1,
    "Deafness|_autosomal_dominant": 1,
    "not_provided|GATA3-related_disorder|Hypoparathyroidism|_deafness|_renal_disease_syndrome": 1,
    "not_provided|GATA3-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Hypoparathyroidism|_deafness|_renal_disease_syndrome": 3,
    "not_provided|Hypoparathyroidism|_deafness|_renal_disease_syndrome|not_specified": 1,
    "not_specified|Hypoparathyroidism|_deafness|_renal_disease_syndrome|not_provided": 2,
    "GATA3-related_disorder|Hypoparathyroidism|_deafness|_renal_disease_syndrome|Inborn_genetic_diseases": 1,
    "B-cell_childhood_acute_lymphoblastic_leukemia": 1,
    "not_provided|B-cell_childhood_acute_lymphoblastic_leukemia": 1,
    "Dominant_congenital_non-syndromic_sensorineural_hearing_loss|not_provided": 1,
    "Stage_5_chronic_kidney_disease|GATA3-related_disorder": 1,
    "Hearing_impairment|Hypoparathyroidism|_deafness|_renal_disease_syndrome|not_provided": 1,
    "Hypoparathyroidism|_deafness|_renal_disease_syndrome|Neurodevelopmental_disorder": 1,
    "CELF2-related_disorder": 7,
    "Developmental_and_epileptic_encephalopathy_97": 14,
    "Developmental_and_epileptic_encephalopathy_97|not_provided": 1,
    "not_provided|CELF2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2A2|2-aminoadipic_2-oxoadipic_aciduria": 1,
    "2-aminoadipic_2-oxoadipic_aciduria": 621,
    "2-aminoadipic_2-oxoadipic_aciduria|not_provided": 20,
    "not_provided|2-aminoadipic_2-oxoadipic_aciduria": 25,
    "Inborn_genetic_diseases|2-aminoadipic_2-oxoadipic_aciduria": 33,
    "DHTKD1-related_disorder": 2,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Q|not_specified|2-aminoadipic_2-oxoadipic_aciduria": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q": 7,
    "not_provided|2-aminoadipic_2-oxoadipic_aciduria|Inborn_genetic_diseases": 3,
    "2-aminoadipic_2-oxoadipic_aciduria|Inborn_genetic_diseases|not_provided": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|not_provided|Inborn_genetic_diseases": 3,
    "2-aminoadipic_2-oxoadipic_aciduria|Inborn_genetic_diseases": 40,
    "2-aminoadipic_2-oxoadipic_aciduria|not_specified": 5,
    "not_provided|not_specified|2-aminoadipic_2-oxoadipic_aciduria": 2,
    "DHTKD1-related_disorder|2-aminoadipic_2-oxoadipic_aciduria": 6,
    "Inborn_genetic_diseases|not_provided|2-aminoadipic_2-oxoadipic_aciduria": 4,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|not_provided|2-aminoadipic_2-oxoadipic_aciduria": 4,
    "not_provided|DHTKD1-related_disorder|2-aminoadipic_2-oxoadipic_aciduria": 2,
    "2-aminoadipic_2-oxoadipic_aciduria|Inborn_genetic_diseases|Tip-toe_gait|not_provided": 1,
    "not_specified|2-aminoadipic_2-oxoadipic_aciduria": 3,
    "not_provided|Inborn_genetic_diseases|2-aminoadipic_2-oxoadipic_aciduria": 4,
    "DHTKD1-related_disorder|not_provided|2-aminoadipic_2-oxoadipic_aciduria|not_specified": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|DHTKD1-related_disorder": 2,
    "not_specified|2-aminoadipic_2-oxoadipic_aciduria|not_provided": 4,
    "2-aminoadipic_2-oxoadipic_aciduria|Charcot-Marie-Tooth_disease_axonal_type_2Q|not_provided": 2,
    "not_specified|2-aminoadipic_2-oxoadipic_aciduria|DHTKD1-related_disorder": 1,
    "Nephrotic_syndrome|2-aminoadipic_2-oxoadipic_aciduria": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|2-aminoadipic_2-oxoadipic_aciduria": 2,
    "not_provided|2-aminoadipic_2-oxoadipic_aciduria|DHTKD1-related_disorder": 2,
    "DHTKD1-related_disorder|not_provided|2-aminoadipic_2-oxoadipic_aciduria": 1,
    "DHTKD1-related_disorder|2-aminoadipic_2-oxoadipic_aciduria|not_provided": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|2-aminoadipic_2-oxoadipic_aciduria|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|2-aminoadipic_2-oxoadipic_aciduria|Charcot-Marie-Tooth_disease_type_2A2": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|not_provided|DHTKD1-related_disorder": 2,
    "not_provided|2-aminoadipic_2-oxoadipic_aciduria|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Q": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|DHTKD1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2Q": 1,
    "not_provided|2-aminoadipic_2-oxoadipic_aciduria|not_specified|Inborn_genetic_diseases|Tip-toe_gait": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Q": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|Charcot-Marie-Tooth_disease_axonal_type_2Q": 2,
    "Charcot-Marie-Tooth_disease_type_2A2|Charcot-Marie-Tooth_disease_axonal_type_2Q": 1,
    "Inborn_genetic_diseases|not_provided|DHTKD1-related_disorder|2-aminoadipic_2-oxoadipic_aciduria": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|Charcot-Marie-Tooth_disease_axonal_type_2Q|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|2-aminoadipic_2-oxoadipic_aciduria|not_provided|not_specified": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|not_specified|Inborn_genetic_diseases": 2,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2Q|not_provided|2-aminoadipic_2-oxoadipic_aciduria": 3,
    "Inborn_disorder_of_lysine_and_hydroxylysine_metabolism|DHTKD1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|2-aminoadipic_2-oxoadipic_aciduria|Charcot-Marie-Tooth_disease_type_2A2|Tip-toe_gait": 1,
    "Distal_amyotrophy": 1,
    "Inborn_genetic_diseases|2-aminoadipic_2-oxoadipic_aciduria|not_provided": 1,
    "DHTKD1-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Q|2-aminoadipic_2-oxoadipic_aciduria|not_provided": 1,
    "not_provided|2-aminoadipic_2-oxoadipic_aciduria|Tip-toe_gait": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|2-aminoadipic_2-oxoadipic_aciduria": 1,
    "2-aminoadipic_2-oxoadipic_aciduria|DHTKD1-related_disorder|not_provided": 1,
    "Amyotrophic_Lateral_Sclerosis|_Recessive|Primary_open_angle_glaucoma": 3,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma": 23,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|not_provided": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12": 10,
    "Amyotrophic_lateral_sclerosis_type_12|not_provided|Primary_open_angle_glaucoma": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|not_provided": 1,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12": 33,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|not_provided": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E": 63,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12": 21,
    "Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma": 43,
    "OPTN-related_disorder|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E": 37,
    "OPTN-related_disorder|not_provided|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12": 1,
    "Amyotrophic_lateral_sclerosis_type_12|not_provided|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|OPTN-related_disorder|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12": 1,
    "not_specified|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_provided": 1,
    "OPTN-related_disorder": 23,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12": 3,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|OPTN-related_disorder|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|not_provided": 2,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|not_provided": 4,
    "Amyotrophic_lateral_sclerosis_type_12": 10,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Inborn_genetic_diseases": 2,
    "Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma": 14,
    "not_provided|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E": 6,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Frontotemporal_dementia": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E": 3,
    "Inborn_genetic_diseases|OPTN-related_disorder": 4,
    "OPTN-related_disorder|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E": 5,
    "not_provided|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Inborn_genetic_diseases": 2,
    "Glaucoma|_normal_tension|_susceptibility_to|Primary_open_angle_glaucoma|not_specified|Amyotrophic_lateral_sclerosis_type_12|not_provided|Glaucoma_1|_open_angle|_E": 1,
    "Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E": 1,
    "not_provided|Glaucoma_1|_open_angle|_E|OPTN-related_disorder|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Inborn_genetic_diseases|Glaucoma_1|_open_angle|_E|not_provided|Glaucoma|_normal_tension|_susceptibility_to": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases": 1,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|not_provided|Inborn_genetic_diseases|OPTN-related_disorder": 1,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Inborn_genetic_diseases|Glaucoma_1|_open_angle|_E": 2,
    "OPTN-related_disorder|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Inborn_genetic_diseases|Glaucoma_1|_open_angle|_E": 1,
    "OPTN-related_disorder|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12": 2,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_provided": 3,
    "Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Amyotrophic_lateral_sclerosis_type_10": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|not_specified|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_12|not_specified|not_provided|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma": 1,
    "OPTN-related_disorder|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E": 2,
    "Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|not_provided": 2,
    "Inborn_genetic_diseases|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12": 4,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|not_provided": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|not_provided|Glaucoma_1|_open_angle|_E": 1,
    "OPTN-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma": 1,
    "OPTN-related_disorder|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_specified|not_provided": 1,
    "not_provided|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases": 1,
    "OPTN-related_disorder|Inborn_genetic_diseases|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_provided": 1,
    "not_specified|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|OPTN-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12": 3,
    "OPTN-related_disorder|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_provided": 1,
    "not_provided|OPTN-related_disorder|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases": 1,
    "not_provided|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Motor_neuron_disease|Inborn_genetic_diseases": 1,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Inborn_genetic_diseases": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Inborn_genetic_diseases|Glaucoma_1|_open_angle|_E": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_specified|not_provided": 1,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_12|not_provided|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_provided|OPTN-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases|OPTN-related_disorder": 1,
    "OPTN-related_disorder|not_provided|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Motor_neuron_disease": 1,
    "not_specified|Primary_open_angle_glaucoma|OPTN-related_disorder|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Inborn_genetic_diseases": 1,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|not_provided|Inborn_genetic_diseases": 1,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Amyotrophic_Lateral_Sclerosis|_Recessive": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "Primary_open_angle_glaucoma|Glaucoma_1|_open_angle|_E|Amyotrophic_lateral_sclerosis_type_12|Inborn_genetic_diseases|OPTN-related_disorder|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|OPTN-related_disorder|Inborn_genetic_diseases": 1,
    "OPTN-related_disorder|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma": 2,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|OPTN-related_disorder|Glaucoma_1|_open_angle|_E": 1,
    "OPTN-related_disorder|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|not_specified|not_provided": 1,
    "not_provided|Glaucoma_1|_open_angle|_E|Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|OPTN-related_disorder": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_lateral_sclerosis_type_12|Glaucoma_1|_open_angle|_E|OPTN-related_disorder": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_12|Primary_open_angle_glaucoma": 1,
    "Primary_open_angle_glaucoma|Amyotrophic_Lateral_Sclerosis|_Recessive|not_provided": 1,
    "Fetal_Cardiomyopathy|Immunodeficiency_80_with_or_without_congenital_cardiomyopathy": 1,
    "Immunodeficiency_80_with_or_without_congenital_cardiomyopathy|Fetal_Cardiomyopathy": 1,
    "Immunodeficiency_80_with_or_without_congenital_cardiomyopathy": 3,
    "Immunodeficiency_80_with_or_without_congenital_cardiomyopathy|not_specified": 1,
    "not_specified|Immunodeficiency_80_with_or_without_congenital_cardiomyopathy": 1,
    "Phytanic_acid_storage_disease": 37,
    "Phytanic_acid_storage_disease|not_provided": 16,
    "not_provided|Phytanic_acid_storage_disease": 13,
    "PHYH-related_disorder|not_provided": 3,
    "Nonsyndromic_cleft_lip_palate|not_provided|Optic_atrophy|not_specified": 1,
    "Phytanic_acid_storage_disease|not_provided|PHYH-related_disorder": 1,
    "Phytanic_acid_storage_disease|not_provided|REFSUM_DISEASE|_ADULT|_1": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa|REFSUM_DISEASE|_ADULT|_1|Phytanic_acid_storage_disease": 1,
    "REFSUM_DISEASE|_ADULT|_1": 3,
    "not_provided|PHYH-related_disorder|Phytanic_acid_storage_disease": 2,
    "Nonsyndromic_cleft_lip_palate|Retinal_dystrophy|not_specified|not_provided|Phytanic_acid_storage_disease|Vitamin_D-dependent_rickets_type_II_with_alopecia": 1,
    "Phytanic_acid_storage_disease|not_provided|not_specified": 2,
    "not_provided|Retinal_dystrophy|Phytanic_acid_storage_disease": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Phytanic_acid_storage_disease": 1,
    "not_provided|Intellectual_disability|Inborn_genetic_diseases|Phytanic_acid_storage_disease": 1,
    "not_provided|Phytanic_acid_storage_disease|PHYH-related_disorder": 2,
    "Phytanic_acid_storage_disease|not_specified|not_provided": 3,
    "PHYH-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Phytanoyl-CoA_hydroxylase_deficiency|Phytanic_acid_storage_disease": 1,
    "not_provided|Phytanic_acid_storage_disease|not_specified": 1,
    "Phytanic_acid_storage_disease|REFSUM_DISEASE|_ADULT|_1": 1,
    "not_provided|Inborn_genetic_diseases|Retinal_dystrophy|Phytanic_acid_storage_disease": 1,
    "Phytanic_acid_storage_disease|not_provided|Retinal_dystrophy": 1,
    "not_provided|REFSUM_DISEASE|_ADULT|_1": 1,
    "Phytanic_acid_storage_disease|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Phytanic_acid_storage_disease|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Phytanic_acid_storage_disease": 1,
    "not_provided|PHYH-related_disorder": 1,
    "Retinal_dystrophy|Phytanic_acid_storage_disease|PHYH-related_disorder|not_provided": 1,
    "not_specified|not_provided|Phytanic_acid_storage_disease|Nonsyndromic_cleft_lip_palate": 1,
    "not_provided|not_specified|Phytanic_acid_storage_disease": 1,
    "Phytanic_acid_storage_disease|Refsum_syndrome|not_provided": 1,
    "REFSUM_DISEASE|_ADULT|_1|PHYH-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|Phytanic_acid_storage_disease|not_provided": 1,
    "not_provided|SEPHS1-related_developmental_delay|VERVERI-BRADY_SYNDROME_2": 1,
    "not_provided|SEPHS1-related_disorder|VERVERI-BRADY_SYNDROME_2": 1,
    "not_provided|VERVERI-BRADY_SYNDROME_2": 1,
    "FRMD4A-related_disorder": 9,
    "Severe_intellectual_disability-corpus_callosum_agenesis-facial_dysmorphism-cerebellar_ataxia_syndrome": 6,
    "not_provided|FRMD4A-related_disorder": 3,
    "Severe_intellectual_disability-corpus_callosum_agenesis-facial_dysmorphism-cerebellar_ataxia_syndrome|not_specified": 1,
    "Severe_intellectual_disability-corpus_callosum_agenesis-facial_dysmorphism-cerebellar_ataxia_syndrome|FRMD4A-related_disorder|not_provided": 1,
    "not_provided|Severe_intellectual_disability-corpus_callosum_agenesis-facial_dysmorphism-cerebellar_ataxia_syndrome": 1,
    "FRMD4A-related_disorder|not_provided": 1,
    "Severe_intellectual_disability-corpus_callosum_agenesis-facial_dysmorphism-cerebellar_ataxia_syndrome|not_provided": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_provided": 3,
    "SUV39H2-related_disorder": 1,
    "DCLRE1C-related_disorder": 2,
    "Histiocytic_medullary_reticulosis": 134,
    "Histiocytic_medullary_reticulosis|not_provided": 1,
    "not_provided|Histiocytic_medullary_reticulosis": 4,
    "Athabaskan_severe_combined_immunodeficiency": 44,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|Inborn_genetic_diseases": 4,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Inborn_genetic_diseases": 9,
    "Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 24,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|not_provided": 4,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 24,
    "DCLRE1C-related_disorder|not_provided|not_specified|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Inborn_genetic_diseases": 3,
    "Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis": 3,
    "not_provided|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 4,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis": 28,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 7,
    "Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 2,
    "Inborn_genetic_diseases|Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 3,
    "Inborn_genetic_diseases|Athabaskan_severe_combined_immunodeficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "DCLRE1C-related_disorder|not_specified|not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 2,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified|not_provided": 1,
    "Athabaskan_severe_combined_immunodeficiency|Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 9,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|Histiocytic_medullary_reticulosis": 2,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|DCLRE1C-related_disorder": 3,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|Athabaskan_severe_combined_immunodeficiency": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 26,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 9,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|Inborn_genetic_diseases|Histiocytic_medullary_reticulosis": 1,
    "not_specified|Histiocytic_medullary_reticulosis": 4,
    "Histiocytic_medullary_reticulosis|Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 5,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_provided": 5,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|Histiocytic_medullary_reticulosis": 2,
    "DCLRE1C-related_disorder|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 2,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified": 1,
    "DCLRE1C-related_disorder|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "not_provided|DCLRE1C-related_disorder|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 2,
    "Severe_combined_immunodeficiency|_partial|Histiocytic_medullary_reticulosis|Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 3,
    "Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|Inborn_genetic_diseases": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 2,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified|not_provided": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_specified|Athabaskan_severe_combined_immunodeficiency": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|Histiocytic_medullary_reticulosis": 2,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_specified": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis": 3,
    "not_provided|Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified|Histiocytic_medullary_reticulosis": 1,
    "not_provided|Histiocytic_medullary_reticulosis|Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "DCLRE1C-related_disorder|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 1,
    "Severe_combined_immunodeficiency_disease|not_specified|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|Histiocytic_medullary_reticulosis|not_specified": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 1,
    "Athabaskan_severe_combined_immunodeficiency|Inborn_genetic_diseases": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Inborn_genetic_diseases|not_specified|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Severe_combined_immunodeficiency_disease": 2,
    "DCLRE1C-related_disorder|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "DCLRE1C-related_disorder|not_provided|Histiocytic_medullary_reticulosis|Inborn_genetic_diseases|Athabaskan_severe_combined_immunodeficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|Aicardi-Goutieres_syndrome_1|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_disease": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Athabaskan_severe_combined_immunodeficiency": 1,
    "Renal_hypodysplasia/aplasia_1|not_provided": 19,
    "Renal_hypodysplasia/aplasia_1": 26,
    "not_provided|ITGA8-related_disorder": 3,
    "ITGA8-related_disorder": 12,
    "ITGA8-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Renal_hypodysplasia/aplasia_1": 2,
    "ITGA8-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|ITGA8-related_disorder": 1,
    "Renal_hypodysplasia/aplasia_1|ITGA8-related_disorder": 1,
    "Renal_hypodysplasia/aplasia_1|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Renal_hypodysplasia/aplasia_1": 1,
    "ITGA8-related_disorder|not_specified|not_provided": 1,
    "Imerslund-Grasbeck_syndrome_type_1": 110,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1": 13,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided": 6,
    "Megaloblastic_anemia|not_provided": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 307,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 12,
    "Proteinuria|_chronic_benign": 15,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 19,
    "Imerslund-Grasbeck_syndrome": 1106,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 50,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 2,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases": 4,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|not_provided": 2,
    "Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 25,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 4,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|not_provided": 1,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 13,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_provided|Imerslund-Grasbeck_syndrome": 2,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 22,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 29,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 29,
    "not_specified|not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|not_provided": 6,
    "CUBN-related_disorder": 31,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 5,
    "not_provided|Imerslund-Grasbeck_syndrome": 18,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided|Imerslund-Grasbeck_syndrome": 11,
    "Inborn_genetic_diseases|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 5,
    "not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 3,
    "not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 20,
    "Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Inborn_genetic_diseases": 1,
    "Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases": 5,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases": 27,
    "not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 2,
    "not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 2,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign": 4,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 40,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder": 10,
    "Imerslund-Grasbeck_syndrome|not_provided": 22,
    "Imerslund-Grasbeck_syndrome|not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1": 2,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided|Imerslund-Grasbeck_syndrome|CUBN-related_disorder": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 3,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 26,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|not_provided": 1,
    "not_specified|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome|not_provided|Imerslund-Grasbeck_syndrome_type_1": 20,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign": 1,
    "CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome": 6,
    "Proteinuria|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|CUBN-related_disorder": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 7,
    "Proteinuria|_chronic_benign|not_provided|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|CUBN-related_disorder": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases": 6,
    "Imerslund-Grasbeck_syndrome_type_1|not_specified|not_provided|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Inborn_genetic_diseases": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_specified": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 3,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 4,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "not_specified|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 2,
    "CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 3,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 4,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1": 4,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided": 4,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 3,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_provided": 5,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided|Imerslund-Grasbeck_syndrome": 7,
    "Megaloblastic_anemia": 3,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "CUBN-related_disorder|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 4,
    "Proteinuria|not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|not_provided": 9,
    "not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome_type_1": 1,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 1,
    "Imerslund-Grasbeck_syndrome|not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 2,
    "Imerslund-Grasbeck_syndrome|not_provided|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder": 2,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 3,
    "Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases": 2,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|CUBN-related_disorder|Proteinuria|not_provided|Imerslund-Grasbeck_syndrome|Chronic_kidney_disease": 1,
    "Imerslund-Grasbeck_syndrome|not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1": 1,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome|not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "Proteinuria|_chronic_benign|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 1,
    "CUBN-related_disorder|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided|CUBN-related_disorder": 1,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided|Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign": 4,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_specified": 1,
    "Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_provided": 3,
    "Imerslund-Grasbeck_syndrome|not_provided|Inborn_genetic_diseases|CUBN-related_disorder": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|not_provided|not_specified": 1,
    "Imerslund-Grasbeck_syndrome|See_cases|not_provided|Imerslund-Grasbeck_syndrome_type_1": 1,
    "not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 2,
    "CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|not_specified|not_provided": 1,
    "not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Focal_segmental_glomerulosclerosis": 1,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 1,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 3,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|CUBN-related_disorder": 1,
    "not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome|not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|not_provided": 1,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 1,
    "not_provided|not_specified|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Proteinuria|_chronic_benign|not_provided|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases|not_provided|Imerslund-Grasbeck_syndrome": 4,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided": 4,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|not_provided|Imerslund-Grasbeck_syndrome": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|Autism_spectrum_disorder|CUBN-related_disorder": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|CUBN-related_disorder": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_provided|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 2,
    "Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|not_provided": 2,
    "not_provided|not_specified|CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 5,
    "not_provided|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "not_provided|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1": 2,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|not_provided": 1,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_specified": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|CUBN-related_disorder": 3,
    "Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|not_provided|Imerslund-Grasbeck_syndrome": 2,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 2,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|not_provided|CUBN-related_disorder": 2,
    "HP:0004341": 1,
    "Inborn_genetic_diseases|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 1,
    "Megaloblastic_anemia|Imerslund-Grasbeck_syndrome": 2,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Inborn_genetic_diseases": 1,
    "CUBN-related_disorder|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome": 1,
    "Inborn_genetic_diseases|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 1,
    "CUBN-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|See_cases|not_provided": 1,
    "Inborn_genetic_diseases|CUBN-related_disorder|not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|not_specified|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|not_specified|Imerslund-Grasbeck_syndrome|not_provided": 1,
    "CUBN-related_disorder|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign": 1,
    "CUBN-related_disorder|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Inborn_genetic_diseases|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|not_provided|CUBN-related_disorder|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder|Imerslund-Grasbeck_syndrome": 3,
    "Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|CUBN-related_disorder": 1,
    "not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Inborn_genetic_diseases": 1,
    "Imerslund-Grasbeck_syndrome|CUBN-related_disorder|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|not_provided": 1,
    "Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided|CUBN-related_disorder|Imerslund-Grasbeck_syndrome|not_specified": 1,
    "Imerslund-Grasbeck_syndrome|not_provided|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|CUBN-related_disorder": 1,
    "Imerslund-Grasbeck_syndrome_type_1|not_provided|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|Proteinuria|_chronic_benign": 1,
    "Imerslund-Grasbeck_syndrome_type_1|Inborn_genetic_diseases|Proteinuria|_chronic_benign": 1,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|Imerslund-Grasbeck_syndrome|not_provided": 1,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_1|Proteinuria|_chronic_benign|CUBN-related_disorder": 1,
    "not_provided|Cataract_30": 2,
    "Developmental_cataract|Cataract_30": 1,
    "Cataract_30": 34,
    "VIM-related_disorder|Cataract_30": 3,
    "Cataract_30|not_specified": 1,
    "Cataract_30|not_provided": 6,
    "VIM-related_disorder": 2,
    "Cataract_30|VIM-related_disorder|not_provided": 1,
    "not_specified|Cataract_30": 3,
    "syndrome_with_premature-aging": 1,
    "Immunodeficiency_51": 682,
    "Congenital_myopathy_11": 4,
    "Congenital_myopathy_11|not_provided": 1,
    "not_provided|Congenital_myopathy_11": 1,
    "HACD1-related_disorder|not_provided": 1,
    "Susceptibility_to_leprosy_and_multibacillary_leprosy|Leprosy|_susceptibility_to|_1": 1,
    "Brugada_syndrome_4": 325,
    "not_specified|CACNB2-related_disorder": 1,
    "not_provided|Brugada_syndrome_4": 12,
    "CACNB2-related_disorder": 6,
    "not_specified|Brugada_syndrome_4": 5,
    "not_specified|Brugada_syndrome_4|not_provided": 3,
    "Short_QT_Syndrome_5|not_specified|not_provided": 1,
    "not_specified|CACNB2-related_disorder|not_provided": 1,
    "Brugada_syndrome|Brugada_syndrome_4": 1,
    "CACNB2-related_disorder|not_specified|not_provided": 1,
    "Brugada_syndrome|Brugada_syndrome_4|not_provided": 1,
    "Brugada_syndrome_4|Cardiovascular_phenotype": 88,
    "Cardiovascular_phenotype|Brugada_syndrome_4": 74,
    "Hypertrophic_cardiomyopathy|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_4|not_specified": 6,
    "not_specified|Brugada_syndrome_4|Cardiovascular_phenotype": 4,
    "Brugada_syndrome_4|Ventricular_fibrillation|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_4": 9,
    "Brugada_syndrome_4|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_4|not_provided|not_specified|Sudden_unexplained_death|Cardiovascular_phenotype|Paroxysmal_familial_ventricular_fibrillation": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_4|not_provided": 4,
    "not_provided|Brugada_syndrome_4|not_specified": 2,
    "Brugada_syndrome_4|not_provided|Cardiovascular_phenotype": 7,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_4|not_specified|Cardiovascular_phenotype": 2,
    "Brugada_syndrome_4|CACNB2-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_4": 4,
    "CACNB2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Cardiomyopathy|Brugada_syndrome_4": 1,
    "CACNB2-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_4": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Brugada_syndrome_4": 1,
    "Brugada_syndrome_4|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|not_specified|Early_repolarization_associated_with_ventricular_fibrillation|Brugada_syndrome|not_provided|Long_QT_syndrome|Brugada_syndrome_4": 1,
    "Brugada_syndrome_4|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_4|CACNB2-related_disorder": 1,
    "Brugada_syndrome_4|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_provided|Brugada_syndrome|Brugada_syndrome_4": 1,
    "not_provided|Brugada_syndrome_4|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_4": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_4|not_specified": 2,
    "Brugada_syndrome_4|not_provided": 4,
    "Brugada_syndrome_4|Cardiovascular_phenotype|Ventricular_fibrillation": 1,
    "Brugada_syndrome_4|not_specified|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Long_QT_syndrome|not_provided|Brugada_syndrome_4|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_4|Cardiac_arrest|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_4|Primary_dilated_cardiomyopathy": 1,
    "CACNB2-related_disorder|not_provided|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_4": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_4|Hypertrophic_cardiomyopathy|not_provided|not_specified": 1,
    "Brugada_syndrome_4|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Brugada_syndrome_4|CACNB2-related_disorder": 2,
    "CACNB2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|Brugada_syndrome_4|Ventricular_tachycardia": 1,
    "not_provided|CACNB2-related_disorder|Brugada_syndrome_4|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome_4|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_4|CACNB2-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Brugada_syndrome_4": 1,
    "Brugada_syndrome_4|Cardiovascular_phenotype|Brugada_syndrome|not_provided": 1,
    "Brugada_syndrome_4|not_provided|Cardiac_arrest|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_4|Sudden_unexplained_death": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_4|not_specified": 3,
    "not_specified|not_provided|Cardiovascular_phenotype|Brugada_syndrome_4|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome_4": 3,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Brugada_syndrome_4|not_specified": 1,
    "Brugada_syndrome_4|Cardiovascular_phenotype|not_specified": 3,
    "not_specified|Brugada_syndrome|not_provided|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "CACNB2-related_disorder|Brugada_syndrome_4|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_4|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Ventricular_tachycardia|Primary_dilated_cardiomyopathy|Supraventricular_tachycardia|not_provided|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "Short_QT_Syndrome_5|not_provided|Brugada_syndrome_4|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_4|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_4|CACNB2-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Brugada_syndrome_4": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_82": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_82|not_provided": 1,
    "NEBL-related_disorder": 6,
    "not_specified|NEBL-related_disorder|Primary_dilated_cardiomyopathy": 2,
    "NEBL-related_disorder|Primary_dilated_cardiomyopathy|not_specified": 5,
    "Primary_dilated_cardiomyopathy|NEBL-related_disorder|not_provided|not_specified": 2,
    "not_provided|NEBL-related_disorder|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Sudden_cardiac_death|not_specified": 1,
    "NEBL-related_disorder|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "NEBL-related_disorder|not_specified|Primary_dilated_cardiomyopathy": 4,
    "not_provided|Primary_dilated_cardiomyopathy|NEBL-related_disorder|not_specified": 4,
    "Primary_dilated_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|NEBL-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|NEBL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|not_specified|Primary_dilated_cardiomyopathy": 4,
    "NEBL-related_disorder|Primary_dilated_cardiomyopathy|not_provided|not_specified": 3,
    "Primary_dilated_cardiomyopathy|NEBL-related_disorder": 2,
    "Sudden_unexplained_death|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Primary_dilated_cardiomyopathy|NEBL-related_disorder|not_specified|not_provided": 1,
    "not_specified|NEBL-related_disorder|Primary_dilated_cardiomyopathy|not_provided": 2,
    "NEBL-related_disorder|not_provided|Primary_dilated_cardiomyopathy|not_specified": 1,
    "not_provided|Primary_dilated_cardiomyopathy|NEBL-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|NEBL-related_disorder|not_specified": 1,
    "not_specified|Primary_dilated_cardiomyopathy|NEBL-related_disorder|not_provided": 1,
    "NEBL-related_Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|NEBL-related_disorder|not_specified": 1,
    "NEBL-related_disorder|Primary_dilated_cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|NEBL-related_disorder|not_specified": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|NEBL-related_disorder|not_specified": 1,
    "NEBL-related_disorder|not_specified|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiac_arrest": 1,
    "Primary_dilated_cardiomyopathy|not_specified|NEBL-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|not_provided|NEBL-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Primary_dilated_cardiomyopathy|NEBL-related_disorder|not_specified": 1,
    "Sudden_unexplained_death|Hypertrophic_cardiomyopathy|sudden_unexplained_death_in_epilepsy|Long_QT_syndrome|NEBL-related_disorder|not_specified|Distal_monosomy_10p|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "NEBL-related_disorder|not_provided|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_specified|NEBL-related_disorder|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Primary_dilated_cardiomyopathy|NEBL-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|not_specified": 1,
    "not_provided|NEBL-related_disorder|not_specified|Primary_dilated_cardiomyopathy": 1,
    "NEBL-related_disorder|not_specified|not_provided": 2,
    "SKIDA1-related_disorder": 8,
    "MLLT10-related_disorder": 12,
    "SPAG6-related_disorder": 1,
    "Stuttering|_familial_persistent|_4": 1,
    "Pancreatic_agenesis_2|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Pancreatic_agenesis_2|not_provided": 2,
    "not_provided|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome": 3,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome": 11,
    "not_provided|Neonatal_insulin-dependent_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome": 1,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|not_provided": 3,
    "PTF1A-related_disorder|not_provided": 3,
    "not_provided|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Inborn_genetic_diseases": 1,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Monogenic_diabetes|not_provided|Inborn_genetic_diseases": 1,
    "Monogenic_diabetes|Pancreatic_agenesis_2|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|not_provided|not_specified": 1,
    "PTF1A-related_disorder": 2,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Pancreatic_agenesis_2": 3,
    "not_provided|Pancreatic_agenesis_2|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome": 2,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|not_specified": 1,
    "Pancreatic_agenesis_2|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Kallikrein|_decreased_urinary_activity_of": 1,
    "Pancreatic_agenesis_2|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome": 2,
    "not_provided|Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|not_specified|Permanent_neonatal_diabetes_mellitus|Pancreatic_beta_cell_agenesis_with_neonatal_diabetes_mellitus|Pancreatic_agenesis_2": 1,
    "Permanent_neonatal_diabetes_mellitus-pancreatic_and_cerebellar_agenesis_syndrome|Monogenic_diabetes": 1,
    "Permanent_neonatal_diabetes_mellitus": 29,
    "not_provided|Permanent_neonatal_diabetes_mellitus": 5,
    "Pancreatic_agenesis_2": 1,
    "OTUD1-related_disorder": 9,
    "not_specified|OTUD1-related_disorder": 1,
    "OTUD1-related_disorder|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30": 65,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided": 21,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_30": 9,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|MYO3A-related_disorder": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_30|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_30|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30": 14,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "Rare_genetic_deafness|not_provided|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided|not_specified": 8,
    "MYO3A-related_disorder": 10,
    "MYO3A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30": 13,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30|not_specified": 9,
    "Hearing_loss|_autosomal_dominant_90|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_30": 1,
    "MYO3A-related_disorder|not_provided|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_30": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_30": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|not_specified|MYO3A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided": 4,
    "MYO3A-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|MYO3A-related_disorder|not_provided|not_specified": 1,
    "not_provided|MYO3A-related_disorder": 2,
    "MYO3A-related_disorder|not_specified|not_provided": 1,
    "Sensorineural_hearing_loss_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_90|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "MYO3A-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30": 3,
    "not_provided|MYO3A-related_disorder|not_specified": 1,
    "MYO3A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_30|not_specified|not_provided": 1,
    "not_specified|MYO3A-related_disorder|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_loss|_autosomal_dominant_90|nonsyndromic_sensorineural_hearing_loss": 1,
    "not_specified|not_provided|MYO3A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "Inborn_genetic_diseases|not_provided|MYO3A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided|MYO3A-related_disorder": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_90|Autosomal_recessive_nonsyndromic_hearing_loss_30|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|not_specified|not_provided": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_30|Inborn_genetic_diseases": 1,
    "MYO3A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "Hearing_loss|_autosomal_dominant_90|Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30|Inborn_genetic_diseases": 1,
    "not_provided|MYO3A-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_30": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_30|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_30|MYO3A-related_disorder|not_specified": 1,
    "Coenzyme_Q10_deficiency|not_specified": 2,
    "not_provided|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 22,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 46,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_provided": 20,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_provided": 2,
    "not_provided|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_specified": 3,
    "not_provided|not_specified|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 3,
    "not_specified|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_provided": 2,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_provided|Coenzyme_Q10_deficiency|not_specified": 1,
    "PDSS1-related_disorder|not_provided|not_specified|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 1,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|PDSS1-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 1,
    "not_provided|PDSS1-related_disorder": 1,
    "not_provided|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|PDSS1-related_disorder": 1,
    "PDSS1-related_disorder|not_specified|not_provided|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 1,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome": 2,
    "Coenzyme_Q10_deficiency|not_provided": 1,
    "PDSS1-related_disorder": 1,
    "Deafness-encephaloneuropathy-obesity-valvulopathy_syndrome|not_specified": 1,
    "Thrombocytopenia_2": 46,
    "Thrombocytopenia_2|not_provided": 26,
    "not_provided|Thrombocytopenia_2": 26,
    "Thrombocytopenia_2|Thrombocytopenia|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|ANKRD26-related_disorder": 5,
    "Thrombocytopenia_2|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Thrombocytopenia_2|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Thrombocytopenia_2|not_provided": 5,
    "ANKRD26-related_disorder": 14,
    "not_provided|Inborn_genetic_diseases|ANKRD26-related_disorder": 5,
    "ANKRD26-related_disorder|not_provided|Inborn_genetic_diseases": 5,
    "Thrombocytopenia_2|Inborn_genetic_diseases": 3,
    "not_provided|ANKRD26-related_disorder|Inborn_genetic_diseases": 4,
    "not_specified|Thrombocytopenia_2": 2,
    "ANKRD26-related_disorder|Thrombocytopenia_2|Thrombocytopenia|Inborn_genetic_diseases|not_provided": 1,
    "Thrombocytopenia_2|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_2": 10,
    "not_specified|Thrombocytopenia_2|not_provided": 9,
    "ANKRD26-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Thrombocytopenia_2": 4,
    "not_provided|not_specified|Thrombocytopenia_2": 1,
    "ANKRD26-related_disorder|not_provided|Thrombocytopenia_2": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Thrombocytopenia_2": 1,
    "not_provided|Thrombocytopenia_2|not_specified": 12,
    "ANKRD26-related_disorder|not_specified|not_provided|Thrombocytopenia_2": 1,
    "ANKRD26-related_disorder|Thrombocytopenia_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Thrombocytopenia_2|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|ANKRD26-related_disorder": 2,
    "not_provided|Thrombocytopenia_2|ANKRD26-related_disorder": 1,
    "not_specified|not_provided|Thrombocytopenia_2": 5,
    "Inborn_genetic_diseases|not_provided|Thrombocytopenia_2": 8,
    "Thrombocytopenia_2|not_specified|ANKRD26-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ANKRD26-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Thrombocytopenia_2": 1,
    "Thrombocytopenia_2|not_specified|not_provided": 4,
    "not_provided|ANKRD26-related_disorder|Thrombocytopenia_2": 1,
    "not_provided|ANKRD26-related_disorder": 6,
    "Thrombocytopenia_2|not_provided|ANKRD26-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Thrombocytopenia_2|not_provided|Inborn_genetic_diseases": 4,
    "Thrombocytopenia|Abnormal_bleeding|Thrombocytopenia_2|not_provided|ANKRD26-related_disorder|not_specified": 1,
    "ANKRD26-related_disorder|Inborn_genetic_diseases": 5,
    "not_specified|not_provided|Thrombocytopenia_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Thrombocytopenia_2": 1,
    "ANKRD26-related_disorder|not_specified|not_provided": 2,
    "not_provided|not_specified|Thrombocytopenia_2|Inborn_genetic_diseases": 1,
    "Thrombocytopenia_2|not_provided|Inborn_genetic_diseases|ANKRD26-related_disorder": 1,
    "Inborn_genetic_diseases|ANKRD26-related_disorder|not_provided": 2,
    "Thrombocytopenia_2|ANKRD26-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|ANKRD26-related_disorder|Thrombocytopenia_2": 1,
    "Inborn_genetic_diseases|not_provided|Thrombocytopenia_2|not_specified": 3,
    "not_provided|not_specified|Thrombocytopenia_2|Thrombocytopenia": 1,
    "not_provided|Thrombocytopenia_2|Thrombocytopenia": 2,
    "ANKRD26-related_disorder|Thrombocytopenia_2|not_provided": 3,
    "Thrombocytopenia_2|ANKRD26-related_disorder|not_provided": 1,
    "ANKRD26-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|ANKRD26-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Thrombocytopenia_2|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|ANKRD26-related_disorder": 2,
    "not_provided|Thrombocytopenia_2|Thrombocytopenia|not_specified": 2,
    "Thrombocytopenia_2|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "ANKRD26-related_disorder|Inborn_genetic_diseases|not_provided|Thrombocytopenia_2": 1,
    "ANKRD26-related_disorder|Thrombocytopenia_2": 1,
    "Inborn_genetic_diseases|not_provided|Thrombocytopenia_2|ANKRD26-related_disorder": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_2|not_provided|ANKRD26-related_disorder|not_specified": 1,
    "Thrombocytopenia_2|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "ANKRD26-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Thrombocytopenia_2|not_provided|ANKRD26-related_disorder": 1,
    "ANKRD26-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|ANKRD26-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Thrombocytopenia_2|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|ANKRD26-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "ANKRD26-related_disorder|Thrombocytopenia_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_2|ANKRD26-related_disorder|not_provided": 1,
    "ANKRD26-related_disorder|Inborn_genetic_diseases|Thrombocytopenia_2|not_specified|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Thrombocytopenia_2": 1,
    "ANKRD26-related_disorder|not_specified|Thrombocytopenia_2|not_provided": 1,
    "not_specified|ANKRD26-related_disorder|Thrombocytopenia_2|not_provided": 1,
    "Thrombocytopenia_2|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|ANKRD26-related_disorder|not_specified": 1,
    "ANKRD26-related_disorder|not_provided|Thrombocytopenia_2|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|ANKRD26-related_disorder": 1,
    "Thrombocytopenia_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_2|ANKRD26-related_disorder|not_specified": 1,
    "ANKRD26-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|Thrombocytopenia_2": 1,
    "ANKRD26-related_disorder|Thrombocytopenia_2|Inborn_genetic_diseases": 1,
    "Thrombocytopenia|ANKRD26-related_disorder|not_specified|not_provided": 1,
    "not_provided|ANKRD26-related_disorder|Thrombocytopenia_2|Thrombocytopenia": 1,
    "ANKRD26-related_disorder|not_provided|not_specified": 1,
    "not_provided|Thrombocytopenia_2|ANKRD26-related_disorder|Thrombocytopenia": 1,
    "Thrombocytopenia|not_provided|Thrombocytopenia_2|not_specified": 1,
    "Inherited_bleeding_disorder|_platelet-type|Thrombocytopenia_2|Thrombocytopenia|not_provided": 1,
    "Thrombocytopenia_2|not_provided|Thrombocytopenia": 2,
    "Thrombocytopenia_2|Thrombocytopenia": 1,
    "Thrombocytopenia|not_provided|Thrombocytopenia_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Thrombocytopenia_2|Thrombocytopenia|not_provided": 1,
    "Optic_atrophy_11|not_provided": 5,
    "Optic_atrophy_11": 3,
    "not_provided|Optic_atrophy_11": 1,
    "YME1L1-related_disorder": 1,
    "not_provided|YME1L1-related_disorder": 1,
    "not_specified|Retinal_dystrophy|Microcephaly": 1,
    "YME1L1-related_disorder|not_provided": 2,
    "Thrombocytopenia|not_provided": 3,
    "not_specified|not_provided|Thrombocytopenia": 8,
    "not_specified|Thrombocytopenia|not_provided": 2,
    "not_provided|not_specified|Thrombocytopenia": 3,
    "MASTL-related_disorder": 13,
    "not_specified|Thrombocytopenia": 1,
    "Thrombocytopenia|MASTL-related_disorder": 3,
    "MASTL-related_disorder|not_specified": 1,
    "MASTL-related_disorder|Thrombocytopenia": 1,
    "MASTL-related_disorder|Thrombocytopenia|not_provided": 1,
    "Thrombocytopenia|not_provided|MASTL-related_disorder": 1,
    "Autosomal_dominant_thrombocytopenia": 1,
    "Thrombocytopenia|MASTL-related_disorder|not_specified": 1,
    "Thrombocytopenia|MASTL-related_disorder|not_provided": 1,
    "Scimitar_anomaly|_multiple_cardiac_malformations|_and_craniofacial_and_central_nervous_system_abnormalities": 1,
    "not_specified|Thrombocytopenia_2|Thrombocytopenia|not_provided": 1,
    "not_provided|Thrombocytopenia|not_specified": 1,
    "Retinal_dystrophy_with_leukodystrophy": 5,
    "ACBD5-related_disorder|not_provided": 5,
    "Retinal_dystrophy_with_leukodystrophy|not_provided": 4,
    "not_provided|Retinal_dystrophy_with_leukodystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Retinal_dystrophy_with_leukodystrophy": 2,
    "ACBD5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ACBD5-related_disorder": 1,
    "not_provided|ACBD5-related_disorder": 4,
    "Warburg_micro_syndrome_3": 96,
    "not_provided|Warburg_micro_syndrome_3": 5,
    "Warburg_micro_syndrome_3|not_specified": 1,
    "not_provided|Warburg_micro_syndrome_3|RAB18-related_disorder": 1,
    "RAB18-related_disorder": 3,
    "Warburg_micro_syndrome_3|not_provided": 10,
    "not_provided|Warburg_micro_syndrome|Warburg_micro_syndrome_3|RAB18-related_disorder|not_specified": 1,
    "not_provided|not_specified|RAB18-related_disorder": 1,
    "RAB18-related_disorder|Warburg_micro_syndrome_3": 1,
    "Warburg_micro_syndrome_3|not_provided|Inborn_genetic_diseases": 1,
    "RAB18-related_disorder|not_provided": 1,
    "not_provided|Warburg_micro_syndrome_3|RAB18-related_disorder|not_specified": 1,
    "MKX-related_disorder": 3,
    "Primary_ciliary_dyskinesia_23": 290,
    "Primary_ciliary_dyskinesia_23|not_provided|Primary_ciliary_dyskinesia": 4,
    "Primary_ciliary_dyskinesia_23|Primary_ciliary_dyskinesia": 43,
    "Primary_ciliary_dyskinesia_23|Primary_ciliary_dyskinesia|not_provided": 5,
    "not_provided|Primary_ciliary_dyskinesia|ODAD2-related_disorder|Primary_ciliary_dyskinesia_23": 3,
    "ODAD2-related_disorder": 8,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23": 59,
    "Primary_ciliary_dyskinesia|ODAD2-related_disorder|not_provided|Primary_ciliary_dyskinesia_23": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23|not_provided": 5,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_23": 12,
    "not_provided|Primary_ciliary_dyskinesia_23|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_23|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia|Male_infertility": 1,
    "Primary_ciliary_dyskinesia_23|not_provided": 6,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23|ODAD2-related_disorder": 2,
    "not_provided|Primary_ciliary_dyskinesia_23": 10,
    "ODAD2-related_disorder|Primary_ciliary_dyskinesia_23|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23": 5,
    "ODAD2-related_disorder|Primary_ciliary_dyskinesia_23|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23|not_provided|ODAD2-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Male_infertility|Primary_ciliary_dyskinesia_23": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23": 1,
    "ODAD2-related_disorder|Primary_ciliary_dyskinesia_23": 2,
    "Primary_ciliary_dyskinesia|ODAD2-related_disorder|Primary_ciliary_dyskinesia_23": 2,
    "Primary_ciliary_dyskinesia_23|ODAD2-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_23|Primary_ciliary_dyskinesia|not_provided|not_specified": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_23|ODAD2-related_disorder": 1,
    "Primary_ciliary_dyskinesia_23|Primary_ciliary_dyskinesia|not_specified": 1,
    "not_provided|Primary_ciliary_dyskinesia_23|not_specified": 1,
    "DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 55,
    "not_provided|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation|DeSanto-Shinawi_syndrome": 1,
    "WAC-related_disorder": 8,
    "DeSanto-Shinawi_syndrome|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 1,
    "DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation|not_provided": 9,
    "Inborn_genetic_diseases|not_provided|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 1,
    "not_provided|WAC-related_disorder": 4,
    "WAC-related_disorder|not_provided": 3,
    "DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation|Inborn_genetic_diseases": 2,
    "not_provided|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 6,
    "DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation|not_provided|Rare_genetic_intellectual_disability": 1,
    "Inborn_genetic_diseases|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 2,
    "WAC-related_neurodevelopmental_disorder|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 1,
    "DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation|Inborn_genetic_diseases|not_provided": 1,
    "WAC-related_disorder|Inborn_genetic_diseases|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation": 1,
    "DeSanto-Shinawi_syndrome": 4,
    "not_provided|WAC-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|WAC-related_disorder": 2,
    "not_provided|Neurodevelopmental_abnormality|DeSanto-Shinawi_syndrome_due_to_WAC_point_mutation|Intellectual_disability": 1,
    "not_provided|Myofibrillar_myopathy_10": 2,
    "SVIL-related_disorder|not_provided": 1,
    "Myofibrillar_myopathy_10": 5,
    "SVIL-related_disorder": 4,
    "SVIL-related_disorder|not_specified": 1,
    "not_specified|SVIL-related_disorder|not_provided": 1,
    "not_specified|Myofibrillar_myopathy_10": 1,
    "Spastic_ataxia_4": 4,
    "not_specified|MTPAP-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spastic_ataxia_4": 1,
    "not_provided|Inborn_genetic_diseases|Spastic_ataxia_4": 1,
    "Spastic_ataxia_4|not_provided": 2,
    "not_specified|not_provided|MTPAP-related_disorder": 1,
    "MTPAP-related_disorder": 2,
    "MTPAP-related_disorder|not_specified|not_provided": 2,
    "not_provided|Spastic_ataxia_4|MTPAP-related_disorder": 1,
    "Spastic_ataxia_4|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Spastic_ataxia_4|not_provided": 1,
    "not_provided|not_specified|MTPAP-related_disorder": 1,
    "MTPAP-related_disorder|not_provided": 1,
    "not_provided|not_specified|Spastic_ataxia_4": 1,
    "not_specified|MAP3K8-related_disorder|not_provided": 1,
    "MAP3K8-related_disorder|not_provided": 5,
    "MAP3K8-related_disorder": 3,
    "not_provided|MAP3K8-related_disorder": 4,
    "Posterior_polymorphous_corneal_dystrophy_3": 5,
    "not_provided|Corneal_dystrophy|_Fuchs_endothelial|_6|Posterior_polymorphous_corneal_dystrophy_3": 3,
    "not_specified|Corneal_dystrophy|_Fuchs_endothelial|_6|ZEB1-related_disorder|not_provided": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_6": 3,
    "Posterior_polymorphous_corneal_dystrophy_3|Corneal_dystrophy|_Fuchs_endothelial|_6": 1,
    "Posterior_polymorphous_corneal_dystrophy": 36,
    "Posterior_polymorphous_corneal_dystrophy_1": 5,
    "ZEB1-related_disorder": 5,
    "Visual_loss|Posterior_polymorphous_corneal_dystrophy|Glaucoma|Inborn_genetic_diseases|not_provided": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_6|Corneal_dystrophy": 1,
    "Posterior_polymorphous_corneal_dystrophy_3|Corneal_dystrophy|_Fuchs_endothelial|_6|ZEB1-related_disorder|not_provided": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_6|not_provided|not_specified": 1,
    "Attention_deficit_hyperactivity_disorder|Global_developmental_delay|Brain_atrophy|Seizure|Hypoplasia_of_the_corpus_callosum": 1,
    "Global_developmental_delay|Respiratory_distress|Seizure|Abnormal_facial_shape|Intellectual_disability|Severe_muscular_hypotonia|KIF5B-related_developmental_disorder": 1,
    "Feeding_difficulties|Intellectual_disability|Severe_muscular_hypotonia|Fatigable_weakness_of_swallowing_muscles": 1,
    "Feeding_difficulties_in_infancy|Hypotonia|Motor_delay|not_provided": 1,
    "Ophthalmoplegia|Primary_dilated_cardiomyopathy|Multiple_joint_contractures|Skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "KIF5B-related_disease": 1,
    "KIF5B-related_developmental_disorder": 1,
    "KIF5B-related_skeletal_dysplasia": 1,
    "not_provided|KIF5B-related_osteogenesis_imperfecta_syndrome": 1,
    "NRP1-related_disorder": 198,
    "not_specified|NRP1-related_disorder": 25,
    "NRP1-related_disorder|not_provided": 5,
    "not_provided|NRP1-related_disorder": 5,
    "NRP1-related_disorder|not_specified": 4,
    "PARD3-related_disorder": 28,
    "not_provided|PARD3-related_disorder": 5,
    "PARD3-related_disorder|not_provided": 3,
    "BMS1-related_disorder|not_provided": 5,
    "not_provided|BMS1-related_disorder": 8,
    "BMS1-related_disorder": 14,
    "Aplasia_cutis_congenita": 4,
    "not_provided|BMS1-related_disorder|not_specified": 1,
    "Multiple_endocrine_neoplasia_type_2A": 59,
    "Multiple_endocrine_neoplasia|Hirschsprung_Disease|_Dominant|not_provided|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 2,
    "Hirschsprung_Disease|_Dominant|Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 2,
    "Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia": 6,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|not_provided|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia": 1,
    "Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 1,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 2,
    "Multiple_endocrine_neoplasia_type_2A|not_provided|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|RET-related_disorder": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 361,
    "Multiple_endocrine_neoplasia|_type_2": 1122,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 20,
    "not_provided|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|not_specified|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 518,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided": 19,
    "Malignant_tumor_of_breast|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 25,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 20,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "Multiple_endocrine_neoplasia|_type_2|Breast_carcinoma|Family_history_of_cancer": 1,
    "RET-related_disorder": 32,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 2,
    "not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "not_provided|not_specified|Aganglionic_megacolon|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 3,
    "Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2": 13,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_specified|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2": 4,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 23,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Renal_hypodysplasia/aplasia_1": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 10,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 2,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 2,
    "Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia|not_specified|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 3,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 1,
    "Ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|not_specified|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided": 13,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|RET-related_disorder": 3,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|RET-related_disorder|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 2,
    "Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_specified|not_provided": 1,
    "Multiple_endocrine_neoplasia|Hirschsprung_Disease|_Dominant|not_provided|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|not_provided": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "RET-related_disorder|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Congenital_central_hypoventilation|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|not_provided|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Renal_hypodysplasia/aplasia_1": 1,
    "Ovarian_cancer|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|not_provided|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Hereditary_cancer|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Ovarian_cancer|Hirschsprung_disease|_susceptibility_to|_1|not_specified|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 2,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 20,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 6,
    "Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Congenital_central_hypoventilation|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 2,
    "Hereditary_cancer-predisposing_syndrome|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 8,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A": 13,
    "Multiple_endocrine_neoplasia|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 5,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|not_provided|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Appendicitis|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Aganglionic_megacolon|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|not_specified|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 10,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Medulloblastoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|not_provided|RET-related_disorder|not_specified|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2": 4,
    "Multiple_endocrine_neoplasia|_type_2|not_specified": 7,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_hypodysplasia/aplasia_1|RET-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 6,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 8,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|not_provided|Renal_hypodysplasia/aplasia_1|not_specified|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|See_cases": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2": 7,
    "Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|RET-related_disorder|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Hirschsprung_Disease|_Dominant|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|not_provided|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "not_provided|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Malignant_tumor_of_breast": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 5,
    "Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 2,
    "not_specified|Pheochromocytoma|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 16,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "Aganglionic_megacolon|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 33,
    "not_specified|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 37,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 18,
    "not_provided|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia_type_2B|not_specified|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 27,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 3,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 1,
    "Abnormality_of_the_digestive_system": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Medullary_thyroid_carcinoma|not_specified": 1,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 13,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Multiple_endocrine_neoplasia_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A": 2,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|not_provided": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "RET-related_disorder|not_specified|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|not_provided|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "not_provided|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B": 2,
    "Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_Disease|_Dominant|Multiple_endocrine_neoplasia|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "RET-related_disorder|Congenital_central_hypoventilation|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 2,
    "Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Congenital_central_hypoventilation|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 2,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|not_provided|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B": 4,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 2,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 2,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "Ependymoma|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2": 1,
    "Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|RET-related_disorder|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia_type_2A|not_specified|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Renal_hypodysplasia/aplasia_1": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2": 3,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 8,
    "Sensorineural_hearing_loss_disorder|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|not_provided": 2,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Pheochromocytoma": 5,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Pilocytic_astrocytoma|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_specified|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|RET-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 2,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Pheochromocytoma|Hirschsprung_Disease|_Dominant|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Appendicitis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Congenital_central_hypoventilation": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|not_specified|not_provided|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Multiple_endocrine_neoplasia_type_2B|not_provided|Multiple_endocrine_neoplasia|_type_2|Medullary_thyroid_carcinoma|not_specified": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 10,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Microcephaly|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|not_specified|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer": 1,
    "Multiple_endocrine_neoplasia|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_specified|Pheochromocytoma|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_provided": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|not_provided|Hirschsprung_Disease|_Dominant|Multiple_endocrine_neoplasia|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 2,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Familial_medullary_thyroid_carcinoma|not_provided": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|MULTIPLE_ENDOCRINE_NEOPLASIA|_TYPE_IIA|_WITH_HIRSCHSPRUNG_DISEASE|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Aganglionic_megacolon|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|MEN2_phenotype:_Unclassified": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Congenital_central_hypoventilation|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_2A|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Aganglionic_megacolon|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|MEN2_phenotype:_Unclassified": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MULTIPLE_ENDOCRINE_NEOPLASIA|_TYPE_IIA|_WITH_HIRSCHSPRUNG_DISEASE|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|RET-related_disorder|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_provided|not_specified": 1,
    "MULTIPLE_ENDOCRINE_NEOPLASIA|_TYPE_IIA|_WITHOUT_PHEOCHROMOCYTOMA": 1,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|not_provided|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|Thyroid_gland_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|MEN2_phenotype:_Unclassified": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|not_specified|not_provided|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Congenital_anomaly_of_kidney_and_urinary_tract|not_specified|Multiple_endocrine_neoplasia_type_2B": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Appendicitis|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia|not_specified|Multiple_endocrine_neoplasia_type_2A|Elevated_basal_serum_calcitonin|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|not_provided|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Congenital_central_hypoventilation|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|not_provided": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|MEN2_phenotype:_Unclassified|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|RET-related_disorder|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|not_specified": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Prostate_neoplasm|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "RET-related_disorder|Aganglionic_megacolon|Multiple_endocrine_neoplasia|_type_2|not_specified|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Renal_hypodysplasia/aplasia_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|Pheochromocytoma|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 3,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Megacolon|Abnormal_facial_shape": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hereditary_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|RET-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Congenital_central_hypoventilation|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hepatocellular_carcinoma|Familial_medullary_thyroid_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|MEN2_phenotype:_Unclassified|not_provided": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Appendicitis|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_specified|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Renal_hypodysplasia/aplasia_1|Familial_cancer_of_breast": 1,
    "not_specified|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|not_specified|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Congenital_central_hypoventilation|Renal_hypodysplasia/aplasia_1|not_provided|Ovarian_cancer|Multiple_endocrine_neoplasia|_type_2|MEN2_phenotype:_Unclassified": 1,
    "MEN2_phenotype:_Unclassified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "not_provided|Pheochromocytoma|not_specified|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 1,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Aganglionic_megacolon": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Congenital_central_hypoventilation|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_provided": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hirschsprung_Disease|_Dominant|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|RET-related_disorder": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|not_specified|Renal_hypodysplasia/aplasia_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 2,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_specified|Aganglionic_megacolon|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|RET-related_disorder|Multiple_endocrine_neoplasia_type_2A|not_provided": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|not_provided|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Congenital_central_hypoventilation|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|not_specified|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_2B|RET-related_disorder|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_provided|Familial_medullary_thyroid_carcinoma|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Renal_hypodysplasia/aplasia_1|Hirschsprung_Disease|_Dominant|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|Pheochromocytoma": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Congenital_central_hypoventilation|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Medullary_thyroid_carcinoma|not_provided|Renal_hypoplasia/aplasia|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia|_type_2|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|RET-related_disorder": 1,
    "Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_II|Medullary_thyroid_carcinoma|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|MEN2_phenotype:_Unclassified": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|RET-related_disorder|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|RET-related_disorder": 1,
    "RET-related_disorder|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Thyroid_carcinoma|_sporadic_medullary|Short_stature|Gingival_overgrowth|Tetralogy_of_Fallot|Hypothyroidism|Constipation|Hypertelorism|Thick_vermilion_border|Joint_hypermobility": 1,
    "Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|not_provided": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hirschsprung_Disease|_Dominant|Renal_hypodysplasia/aplasia_1": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon": 1,
    "not_specified|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|not_specified|Multiple_endocrine_neoplasia_type_2A|not_provided|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|not_specified": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Malignant_tumor_of_breast": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Congenital_central_hypoventilation|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Renal_hypodysplasia/aplasia_1|not_specified|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Renal_hypodysplasia/aplasia_1|not_provided|Multiple_endocrine_neoplasia": 1,
    "Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Appendicitis|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Renal_hypodysplasia/aplasia_1": 1,
    "RET-related_disorder|Multiple_endocrine_neoplasia_type_2A": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|not_provided|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Ovarian_cancer": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|not_specified|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B": 2,
    "RET-related_disorder|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Renal_hypodysplasia/aplasia_1|not_specified|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|Pheochromocytoma": 1,
    "RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|RET-related_disorder|Ewing_sarcoma_of_soft_tissue|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_2|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_specified": 2,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_specified|Aganglionic_megacolon|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "RET-related_disorder|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Appendicitis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer|Hirschsprung_disease|_susceptibility_to|_1|not_specified|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|not_specified|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|not_specified|Multiple_endocrine_neoplasia|_type_2": 1,
    "Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|not_specified|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_2|Aganglionic_megacolon": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_2B|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|not_provided|Multiple_endocrine_neoplasia|_type_2": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Familial_medullary_thyroid_carcinoma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|not_provided|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|_type_2|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hirschsprung_disease|_susceptibility_to|_1|not_specified|not_provided|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia_type_2A|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|RET-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia_type_2B|Hirschsprung_disease|_susceptibility_to|_1|not_specified|Pheochromocytoma": 1,
    "Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_2|not_provided|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Renal_hypodysplasia/aplasia_1|Pheochromocytoma": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Familial_medullary_thyroid_carcinoma|Pheochromocytoma|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia_type_2B|Multiple_endocrine_neoplasia|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_specified|Multiple_endocrine_neoplasia_type_2A|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2B|Pheochromocytoma|Familial_medullary_thyroid_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_2|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|RET-related_disorder|not_specified": 1,
    "Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|not_specified": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Pheochromocytoma|not_provided|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 3,
    "Pheochromocytoma|Hirschsprung_Disease|_Dominant|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 9,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Pheochromocytoma": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia|Hirschsprung_Disease|_Dominant|Renal_hypodysplasia/aplasia_1": 2,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|Hirschsprung_Disease|_Dominant|Renal_hypodysplasia/aplasia_1": 4,
    "Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia": 5,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|not_provided|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1|Pheochromocytoma|Hirschsprung_Disease|_Dominant": 1,
    "Multiple_endocrine_neoplasia|not_provided|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "Pheochromocytoma|Hirschsprung_disease|_susceptibility_to|_1|not_provided|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 1,
    "not_provided|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Multiple_endocrine_neoplasia|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Renal_hypodysplasia/aplasia_1|Hirschsprung_Disease|_Dominant|Pheochromocytoma|Multiple_endocrine_neoplasia": 1,
    "Pheochromocytoma|Multiple_endocrine_neoplasia|Hirschsprung_disease|_susceptibility_to|_1|Renal_hypodysplasia/aplasia_1": 3,
    "Multiple_endocrine_neoplasia|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 5,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1|Pheochromocytoma|Multiple_endocrine_neoplasia|Renal_hypodysplasia/aplasia_1": 1,
    "Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Hirschsprung_disease|_protection_against|not_provided|Hirschsprung_disease|_susceptibility_to|_1|Multiple_endocrine_neoplasia_type_2A|Multiple_endocrine_neoplasia|Pheochromocytoma|Renal_hypodysplasia/aplasia_1": 1,
    "not_provided|CXCL12-related_disorder": 2,
    "CXCL12-related_disorder": 4,
    "Asthma|_diminished_response_to_antileukotriene_treatment_in|Atherosclerosis|_susceptibility_to": 1,
    "Prostate_cancer|_hereditary|_13": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5": 117,
    "GDF2-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_5": 2,
    "Cardiovascular_phenotype|GDF2-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_5|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|not_provided": 4,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_5": 35,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|Pulmonary_arterial_hypertension": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype": 28,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_5|not_provided": 5,
    "Cardiovascular_phenotype|GDF2-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_5": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_5": 4,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|not_specified": 3,
    "GDF2-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|GDF2-related_disorder": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|not_specified|Cardiovascular_phenotype": 1,
    "GDF2-related_disorder": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype|GDF2-related_disorder": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|not_provided|Cardiovascular_phenotype": 3,
    "GDF2-related_disorder|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_5": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype": 1,
    "GDF2-related_disorder|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype|Pulmonary_arterial_hypertension": 1,
    "Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_5": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|not_provided|GDF2-related_disorder": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_5|Cardiovascular_phenotype|GDF2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_5": 1,
    "not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_5": 1,
    "Retinitis_pigmentosa_66|Retinitis_pigmentosa|not_provided": 7,
    "Retinitis_pigmentosa_66": 13,
    "Retinitis_pigmentosa_66|not_provided": 5,
    "not_provided|Retinitis_pigmentosa_66": 7,
    "Retinitis_pigmentosa|not_provided|RBP3-related_disorder": 2,
    "RBP3-related_disorder|not_provided": 6,
    "not_provided|Retinitis_pigmentosa_66|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_66|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_66": 1,
    "RBP3-related_disorder": 3,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Retinitis_pigmentosa_66|not_provided": 1,
    "Retinitis_pigmentosa_66|Optic_atrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_66|not_specified|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_66|not_provided": 2,
    "not_specified|Retinitis_pigmentosa_66|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_66|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_66": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_66|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_66": 1,
    "Retinitis_pigmentosa_66|not_provided|RBP3-related_disorder": 1,
    "RBP3-related_disorder|Retinitis_pigmentosa_66|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|RBP3-related_disorder": 4,
    "RBP3-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_66|not_provided": 1,
    "Retinal_dystrophy|RBP3-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_66|RBP3-related_disorder|not_specified": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_66": 2,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "RBP3-related_disorder|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_66": 1,
    "not_provided|RBP3-related_disorder|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_66": 1,
    "Retinitis_pigmentosa|not_provided|not_specified|Retinitis_pigmentosa_66|Retinal_dystrophy": 1,
    "not_provided|RBP3-related_disorder|Retinitis_pigmentosa_66": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_66": 1,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "MAPK8-related_disorder": 2,
    "WDFY4-related_disorder": 17,
    "WDFY4-related_disorder|not_specified": 1,
    "not_specified|WDFY4-related_disorder": 3,
    "CARDIOMYOPATHY|_DILATED|_1QQ": 3,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 33,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5": 8,
    "Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1": 10,
    "not_provided|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided": 9,
    "Cockayne_syndrome|COFS_syndrome|Macular_degeneration": 8,
    "Cockayne_syndrome|COFS_syndrome|Macular_degeneration|not_provided": 2,
    "not_provided|Cockayne_syndrome|COFS_syndrome|Macular_degeneration": 6,
    "Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5": 3,
    "Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2": 4,
    "Cerebrooculofacioskeletal_syndrome_1|not_provided|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2": 5,
    "COFS_syndrome|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Macular_degeneration|Cockayne_syndrome": 1,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided": 2,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided": 9,
    "Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|not_provided|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Lung_cancer|Inborn_genetic_diseases|Age_related_macular_degeneration_5": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 14,
    "Cerebrooculofacioskeletal_syndrome_1|not_provided|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5": 6,
    "not_provided|ERCC6-related_disorder": 6,
    "Cockayne_syndrome|Macular_degeneration|COFS_syndrome|not_provided|not_specified": 2,
    "not_specified|ERCC6-related_disorder|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|not_provided|Cockayne_syndrome_type_2|Intellectual_disability|Age_related_macular_degeneration_5": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|not_provided|Cockayne_syndrome_type_2": 16,
    "Cerebrooculofacioskeletal_syndrome_1|Lung_carcinoma|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Cockayne_syndrome_type_2": 79,
    "ERCC6-related_disorder|not_provided": 12,
    "Cerebrooculofacioskeletal_syndrome_1|Lung_carcinoma|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|not_provided": 2,
    "not_provided|Cockayne_spectrum_with_or_without_cerebrooculofacioskeletal_syndrome|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "ERCC6-related_disorder|DE_SANCTIS-CACCHIONE_SYNDROME|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME": 12,
    "Premature_ovarian_failure_11": 2,
    "not_provided|Age_related_macular_degeneration_5|Premature_ovarian_failure_11|Lung_cancer|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_specified": 1,
    "not_provided|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 4,
    "Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Premature_ovarian_failure_11": 1,
    "Cerebrooculofacioskeletal_syndrome_1|not_provided": 2,
    "not_provided|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME": 4,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cockayne_syndrome|not_provided": 3,
    "not_specified|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Lung_cancer|COFS_syndrome|Macular_degeneration|not_provided|Cockayne_syndrome": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|not_provided": 2,
    "not_provided|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5": 2,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|not_provided": 1,
    "Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_1": 9,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided|Age_related_macular_degeneration_5": 3,
    "not_specified|not_provided|ERCC6-related_disorder": 2,
    "ERCC6-related_disorder|not_provided|Cerebrooculofacioskeletal_syndrome_1": 1,
    "ERCC6-related_disorder": 7,
    "Cockayne_syndrome|Macular_degeneration|COFS_syndrome|not_specified|not_provided": 2,
    "not_provided|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Lung_cancer|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Age_related_macular_degeneration_5|Premature_ovarian_failure_11": 17,
    "Cockayne_syndrome_type_2|not_provided": 8,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|not_provided": 3,
    "not_provided|Cockayne_syndrome_type_2": 10,
    "Cockayne_syndrome|not_provided": 2,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided|Age_related_macular_degeneration_5": 2,
    "DE_SANCTIS-CACCHIONE_SYNDROME|not_provided": 2,
    "DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Lung_cancer|not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_5": 1,
    "not_specified|not_provided|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_5": 1,
    "not_provided|ERCC6-related_disorder|COFS_syndrome|Macular_degeneration|Cockayne_syndrome": 1,
    "not_provided|not_specified|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Lung_carcinoma|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Inborn_genetic_diseases|COFS_syndrome|Cockayne_syndrome|not_specified|not_provided|Cone-rod_dystrophy|Macular_degeneration|Intellectual_disability": 2,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|ERCC6-related_disorder|not_provided|Age_related_macular_degeneration_5": 1,
    "not_specified|not_provided|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 2,
    "DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Lung_cancer|not_provided": 2,
    "not_specified|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5": 1,
    "not_specified|Cerebrooculofacioskeletal_syndrome_1": 1,
    "Cockayne_syndrome|ERCC6-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5": 2,
    "COFS_syndrome|ERCC6-related_disorder|Cockayne_syndrome|not_provided|Macular_degeneration": 1,
    "Premature_ovarian_failure_11|UV-sensitive_syndrome_1|Lung_cancer|Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|not_specified": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_1|Inborn_genetic_diseases": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Lung_cancer|not_provided": 4,
    "Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|not_provided|Age_related_macular_degeneration_5": 3,
    "not_specified|not_provided|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1": 1,
    "not_provided|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Lung_cancer": 1,
    "not_provided|Cockayne_syndrome|Cockayne_syndrome_type_2": 1,
    "Cockayne_syndrome|not_specified|not_provided|COFS_syndrome|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Macular_degeneration|DE_SANCTIS-CACCHIONE_SYNDROME": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Lung_cancer|ERCC6-related_disorder|not_provided|Age_related_macular_degeneration_5": 1,
    "not_provided|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Premature_ovarian_failure_11|Age_related_macular_degeneration_5": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_5": 1,
    "not_provided|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|ERCC6-related_disorder|Inborn_genetic_diseases": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Cockayne_syndrome|not_provided": 2,
    "Cerebrooculofacioskeletal_syndrome_1|not_specified": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|COFS_syndrome|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Age_related_macular_degeneration_5|Lung_cancer|Macular_degeneration|Cockayne_syndrome": 1,
    "ERCC6-related_disorder|not_specified|not_provided|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "not_specified|Cerebrooculofacioskeletal_syndrome_1|not_provided|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2": 1,
    "ERCC6-related_disorder|Cerebrooculofacioskeletal_syndrome_1|Intellectual_disability|not_provided|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|not_provided": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Cockayne_syndrome_type_2": 2,
    "Premature_ovarian_failure_11|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Inborn_genetic_diseases": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Lung_cancer|not_provided|Cockayne_syndrome": 1,
    "not_provided|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|Lung_cancer|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|DE_SANCTIS-CACCHIONE_SYNDROME|Age_related_macular_degeneration_5|Inborn_genetic_diseases": 1,
    "Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1|not_provided": 1,
    "Age_related_macular_degeneration_5|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Lung_cancer|ERCC6-related_disorder|not_provided": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Lung_cancer|not_provided": 2,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Cockayne_syndrome|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Inborn_genetic_diseases|ERCC6-related_disorder|Cockayne_syndrome|not_provided": 1,
    "Cockayne_syndrome|not_provided|Cockayne_syndrome_type_2": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|Lung_cancer|not_provided": 1,
    "COFS_syndrome|ERCC6-related_disorder|Macular_degeneration|Cockayne_syndrome|not_provided": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|Lung_cancer|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|ERCC6-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|not_provided": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|not_provided|Age_related_macular_degeneration_5": 1,
    "ERCC6-related_disorder|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Age_related_macular_degeneration_5|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Lung_cancer|Cockayne_syndrome_type_2|not_provided": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_specified": 1,
    "not_provided|Age_related_macular_degeneration_5|Premature_ovarian_failure_11|Lung_cancer|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Inborn_genetic_diseases|not_provided|Cockayne_syndrome_type_2": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5|not_provided|Cockayne_syndrome_type_2": 1,
    "not_specified|not_provided|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME": 1,
    "Age_related_macular_degeneration_5|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Lung_cancer|not_provided": 1,
    "not_provided|Cockayne_syndrome_type_2|Inborn_genetic_diseases|not_specified": 1,
    "Cerebrooculofacioskeletal_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|DE_SANCTIS-CACCHIONE_SYNDROME": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|not_specified|not_provided": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Lung_cancer|Age_related_macular_degeneration_5|Premature_ovarian_failure_11|UV-sensitive_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "COFS_syndrome|Cockayne_syndrome|not_specified|not_provided|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Macular_degeneration": 1,
    "not_provided|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|Lung_cancer": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2": 1,
    "not_provided|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Age_related_macular_degeneration_5|Lung_cancer|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1": 1,
    "Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Age_related_macular_degeneration_5|ERCC6-related_disorder|not_provided|not_specified": 1,
    "not_provided|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_specified": 1,
    "Cockayne_syndrome|Cerebrooculofacioskeletal_syndrome_1|not_provided": 1,
    "Cockayne_spectrum_with_or_without_cerebrooculofacioskeletal_syndrome|Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cockayne_syndrome|not_provided": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Cockayne_syndrome_type_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Cockayne_syndrome_type_2|ERCC6-related_disorder": 1,
    "PGBD3-related_disorder": 3,
    "not_specified|Cockayne_syndrome_type_2": 1,
    "Premature_ovarian_failure_11|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|Lung_cancer|not_specified": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|not_specified|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Premature_ovarian_failure_11|DE_SANCTIS-CACCHIONE_SYNDROME|Cockayne_syndrome_type_2|Lung_cancer|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|not_provided|not_specified": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_5|Cockayne_syndrome_type_2|Cerebrooculofacioskeletal_syndrome_1": 1,
    "Age_related_macular_degeneration_5|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Lung_cancer|Lung_carcinoma|not_provided": 1,
    "COFS_syndrome|Cockayne_syndrome|not_specified|not_provided|Macular_degeneration": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Cockayne_syndrome_type_2": 1,
    "not_specified|Age_related_macular_degeneration_5|Inborn_genetic_diseases|Cerebrooculofacioskeletal_syndrome_1|not_provided|Cockayne_syndrome_type_2": 1,
    "Cockayne_syndrome|not_specified|not_provided|COFS_syndrome|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Macular_degeneration|Cockayne_syndrome_type_2": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|not_provided|Cockayne_syndrome_type_2|Inborn_genetic_diseases": 1,
    "ERCC6-related_disorder|not_specified|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|not_provided|Cockayne_syndrome_type_2": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|DE_SANCTIS-CACCHIONE_SYNDROME|not_provided": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Genetic_non-acquired_premature_ovarian_failure|not_provided|Cockayne_syndrome_type_2": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|Age_related_macular_degeneration_5|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Lung_cancer|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|DE_SANCTIS-CACCHIONE_SYNDROME|Age_related_macular_degeneration_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|Age_related_macular_degeneration_5|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|Lung_cancer|DE_SANCTIS-CACCHIONE_SYNDROME|not_provided": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Cockayne_syndrome_type_2|Inborn_genetic_diseases": 1,
    "COFS_syndrome|not_provided|Cockayne_syndrome|Macular_degeneration|not_specified": 1,
    "Inborn_genetic_diseases|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Cockayne_syndrome|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Premature_ovarian_failure_11|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Age_related_macular_degeneration_5|not_provided": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|ERCC6-related_disorder|not_provided": 1,
    "not_provided|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Cockayne_syndrome|not_provided|not_specified|COFS_syndrome|UV-sensitive_syndrome_1|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Macular_degeneration|DE_SANCTIS-CACCHIONE_SYNDROME": 1,
    "Macular_degeneration|COFS_syndrome|Cockayne_syndrome|not_specified|not_provided": 1,
    "Cockayne_syndrome_type_2|Lung_cancer|Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|UV-sensitive_syndrome_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|UV-sensitive_syndrome_1|Premature_ovarian_failure_11|Age_related_macular_degeneration_5|DE_SANCTIS-CACCHIONE_SYNDROME|Lung_cancer|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Cockayne_syndrome|not_provided|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2": 1,
    "Cerebrooculofacioskeletal_syndrome_1|Lung_cancer|Cockayne_syndrome_type_2|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Age_related_macular_degeneration_5|not_provided": 1,
    "not_provided|Cockayne_spectrum_with_or_without_cerebrooculofacioskeletal_syndrome": 1,
    "not_specified|not_provided|COFS_syndrome|UV-sensitive_syndrome_1|DE_SANCTIS-CACCHIONE_SYNDROME|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|Macular_degeneration|Cockayne_syndrome": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Lung_cancer|not_provided|ERCC6-related_disorder|Cockayne_syndrome|See_cases": 1,
    "DE_SANCTIS-CACCHIONE_SYNDROME|Premature_ovarian_failure_11|Cerebrooculofacioskeletal_syndrome_1|UV-sensitive_syndrome_1|Cockayne_syndrome_type_2|Age_related_macular_degeneration_5|Lung_cancer|not_specified": 1,
    "Age_related_macular_degeneration_5|Cerebrooculofacioskeletal_syndrome_1|Cockayne_syndrome_type_2|ERCC6-related_disorder": 1,
    "Cockayne_syndrome|not_provided|COFS_syndrome|Macular_degeneration": 1,
    "not_provided|LUNG_CANCER|_SUSCEPTIBILITY_TO|Age_related_macular_degeneration_5": 1,
    "not_provided|Congenital_myasthenic_syndrome_21": 2,
    "not_provided|SLC18A3-related_disorder|Congenital_myasthenic_syndrome_21": 1,
    "not_provided|CHAT-related_disorder": 1,
    "Congenital_myasthenic_syndrome_21|Inborn_genetic_diseases|not_provided": 2,
    "Congenital_myasthenic_syndrome_21": 10,
    "Congenital_myasthenic_syndrome_21|not_provided": 3,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_21": 1,
    "SLC18A3-related_disorder": 2,
    "not_provided|SLC18A3-related_disorder": 2,
    "SLC18A3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_21": 1,
    "not_provided|Familial_infantile_myasthenia|Congenital_myasthenic_syndrome_21": 1,
    "Familial_infantile_myasthenia|not_provided|not_specified": 3,
    "not_provided|not_specified|Familial_infantile_myasthenia": 2,
    "not_specified|Familial_infantile_myasthenia": 8,
    "Familial_infantile_myasthenia": 712,
    "Inborn_genetic_diseases|Familial_infantile_myasthenia": 26,
    "Familial_infantile_myasthenia|Inborn_genetic_diseases": 26,
    "Familial_infantile_myasthenia|not_provided": 16,
    "not_specified|not_provided|Familial_infantile_myasthenia": 11,
    "not_provided|Inborn_genetic_diseases|Familial_infantile_myasthenia": 1,
    "Familial_infantile_myasthenia|not_specified": 7,
    "CHAT-related_disorder|not_provided": 1,
    "Familial_infantile_myasthenia|not_specified|not_provided": 4,
    "not_provided|Familial_infantile_myasthenia|not_specified": 5,
    "not_provided|Familial_infantile_myasthenia|Inborn_genetic_diseases|CHAT-related_disorder": 1,
    "not_provided|Familial_infantile_myasthenia": 20,
    "Rigidity|Gait_ataxia|Gait_imbalance|Muscle_weakness|Gait_disturbance|Sleep_abnormality": 1,
    "Congenital_myasthenic_syndrome|not_provided|Familial_infantile_myasthenia": 2,
    "Familial_infantile_myasthenia|CHAT-related_disorder": 2,
    "not_specified|not_provided|Familial_infantile_myasthenia|CHAT-related_disorder": 1,
    "Congenital_myasthenic_syndrome|Familial_infantile_myasthenia|not_specified": 1,
    "CHAT-related_disorder|Familial_infantile_myasthenia": 8,
    "not_provided|Familial_infantile_myasthenia|Inborn_genetic_diseases": 2,
    "not_provided|Congenital_myasthenic_syndrome|Familial_infantile_myasthenia": 1,
    "Familial_infantile_myasthenia|not_provided|Congenital_myasthenic_syndrome": 1,
    "Inborn_genetic_diseases|Familial_infantile_myasthenia|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome|Familial_infantile_myasthenia": 7,
    "not_specified|Familial_infantile_myasthenia|CHAT-related_disorder|not_provided": 1,
    "Familial_infantile_myasthenia|CHAT-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome_4C|Familial_infantile_myasthenia": 1,
    "Abnormality_of_the_musculature|Familial_infantile_myasthenia": 1,
    "Aspiration_pneumonia|Progressive_ptosis|Progressive_muscle_weakness|Decreased_activity_of_the_pyruvate_dehydrogenase_complex|Gastroesophageal_reflux|Respiratory_insufficiency|Lactic_acidosis|Apnea|_central_sleep|External_ophthalmoplegia|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Pes_planus|Familial_infantile_myasthenia": 2,
    "not_provided|Familial_infantile_myasthenia|CHAT-related_disorder": 1,
    "Familial_infantile_myasthenia|Inborn_genetic_diseases|CHAT-related_disorder": 1,
    "Inborn_genetic_diseases|Familial_infantile_myasthenia|not_provided": 1,
    "Familial_infantile_myasthenia|Congenital_myasthenic_syndrome": 1,
    "not_provided|Familial_infantile_myasthenia|Congenital_myasthenic_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Familial_infantile_myasthenia": 3,
    "Congenital_myasthenic_syndrome|Familial_infantile_myasthenia|not_provided": 1,
    "not_specified|Familial_infantile_myasthenia|not_provided|CHAT-related_disorder": 1,
    "not_specified|Familial_infantile_myasthenia|not_provided": 1,
    "OGDHL-related_disorder": 17,
    "OGDHL-related_disorder|not_provided": 3,
    "Yoon-Bellen_neurodevelopmental_syndrome": 17,
    "Abnormal_brain_morphology|Yoon-Bellen_neurodevelopmental_syndrome": 1,
    "Inborn_genetic_diseases|Yoon-Bellen_neurodevelopmental_syndrome": 1,
    "OGDHL-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Depression": 1,
    "Yoon-Bellen_neurodevelopmental_syndrome|not_provided": 1,
    "OGDHL-related_disorder|not_specified|not_provided": 1,
    "not_provided|OGDHL-related_disorder|not_specified": 1,
    "Yoon-Bellen_neurodevelopmental_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|OGDHL-related_disorder": 1,
    "OGDHL-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Yoon-Bellen_neurodevelopmental_syndrome|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_8|PRKG1-related_disorder": 1,
    "PRKG1-related_disorder|Aortic_aneurysm|_familial_thoracic_8|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "PRKG1-related_disorder": 7,
    "Aortic_aneurysm|_familial_thoracic_8": 316,
    "Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 56,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_specified": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_8": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8": 38,
    "Aortic_aneurysm|_familial_thoracic_8|not_specified": 14,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_8|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8": 3,
    "Aortic_aneurysm|_familial_thoracic_8|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_provided": 6,
    "Aortic_aneurysm|_familial_thoracic_8|not_provided": 14,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_8": 6,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder|Aortic_aneurysm|_familial_thoracic_8|not_provided": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_specified|PRKG1-related_disorder": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_8": 9,
    "Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 5,
    "Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 2,
    "Aortic_aneurysm|_familial_thoracic_8|PRKG1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_8|not_specified|PRKG1-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_8|PRKG1-related_disorder": 1,
    "not_provided|PRKG1-related_disorder|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|PRKG1-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Aortic_aneurysm|_familial_thoracic_8|PRKG1-related_disorder|not_provided": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_8|not_specified": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_8|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Connective_tissue_disorder|PRKG1-related_disorder|Aortic_aneurysm|_familial_thoracic_8|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_8|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder": 1,
    "Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_8|not_specified": 2,
    "not_provided|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder": 1,
    "PRKG1-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_8|PRKG1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_8|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_8|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_specified|PRKG1-related_disorder": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_8": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|PRKG1-related_disorder|Aortic_aneurysm|_familial_thoracic_8": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_8": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_specified": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_8|not_specified": 1,
    "DKK1-related_disorder": 2,
    "Mannose-binding_lectin_deficiency": 57,
    "not_provided|Mannose-binding_lectin_deficiency": 12,
    "Mannose-binding_lectin_deficiency|not_provided": 9,
    "MBL2-related_disorder|Mannose-binding_lectin_deficiency": 2,
    "not_specified|Mannose-binding_lectin_deficiency|not_provided": 2,
    "Mannose-binding_lectin_deficiency|not_specified": 3,
    "MBL2-related_disorder": 3,
    "MBL2-related_disorder|Mannose-binding_lectin_deficiency|not_specified": 1,
    "MBL2-related_disorder|not_specified": 1,
    "Mannose-binding_lectin_deficiency|not_provided|not_specified": 1,
    "not_specified|not_provided|Mannose-binding_lectin_deficiency": 2,
    "Mannose-binding_lectin_deficiency|not_provided|Cystic_fibrosis": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 6,
    "Usher_syndrome_type_1D": 75,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_specified|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_specified": 1,
    "PCDH15-related_disorder": 11,
    "PCDH15-related_disorder|not_provided": 5,
    "not_provided|PCDH15-related_disorder": 5,
    "Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F": 5,
    "PCDH15-related_disorder|not_specified|not_provided": 3,
    "PCDH15-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided": 7,
    "not_provided|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 3,
    "Usher_syndrome_type_1D|not_provided": 8,
    "not_provided|PCDH15-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_specified": 1,
    "not_specified|PCDH15-related_disorder|not_provided": 2,
    "not_specified|Usher_syndrome_type_1F": 6,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23": 88,
    "not_provided|Usher_syndrome_type_1F": 116,
    "not_specified|Inborn_genetic_diseases|Usher_syndrome_type_1D": 1,
    "not_provided|not_specified|PCDH15-related_disorder": 2,
    "Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_23": 2,
    "not_specified|not_provided|PCDH15-related_disorder": 2,
    "PCDH15-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|PCDH15-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|PCDH15-related_disorder|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Usher_syndrome_type_1|not_provided": 2,
    "Usher_syndrome_type_1|not_provided": 144,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1": 16,
    "Usher_syndrome_type_1F|not_provided": 122,
    "Progressive_cone_dystrophy_(without_rod_involvement)": 1,
    "Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided": 9,
    "Usher_syndrome_type_1F|not_specified|not_provided": 5,
    "not_provided|Usher_syndrome_type_1": 167,
    "not_specified|Usher_syndrome_type_1F|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|PCDH15-related_disorder": 1,
    "Usher_syndrome_type_1F|not_provided|PCDH15-related_disorder": 2,
    "not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F": 6,
    "not_provided|Usher_syndrome_type_1F|Retinal_dystrophy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 12,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "not_specified|not_provided|Usher_syndrome_type_1F|Inborn_genetic_diseases|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1F|not_provided|not_specified": 1,
    "not_specified|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided|Usher_syndrome_type_1|USHER_SYNDROME|_TYPE_ID/F|_DIGENIC": 1,
    "not_specified|not_provided|Usher_syndrome_type_1": 15,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1D|not_provided": 1,
    "Usher_syndrome_type_1|Inborn_genetic_diseases": 5,
    "not_provided|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1F": 2,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1F": 3,
    "PCDH15-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F": 4,
    "not_provided|Usher_syndrome_type_1|not_specified": 20,
    "Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D": 2,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F": 4,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Usher_syndrome_type_1F|not_specified|Usher_syndrome_type_1|not_provided": 1,
    "Usher_syndrome_type_1|PCDH15-related_disorder|not_specified|not_provided": 1,
    "Usher_syndrome_type_1F|not_specified": 6,
    "Inborn_genetic_diseases|Usher_syndrome_type_1F|not_provided": 5,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|PCDH15-related_disorder|not_specified|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1F|Inborn_genetic_diseases|not_specified": 2,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided": 8,
    "not_provided|Usher_syndrome_type_1F|not_specified": 8,
    "not_provided|not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1F": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1F|Usher_syndrome_type_1|PCDH15-related_disorder|not_specified": 1,
    "not_provided|PCDH15-related_disorder|Usher_syndrome_type_1F|not_specified": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|not_specified|not_provided": 14,
    "PCDH15-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_specified|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa-deafness_syndrome|Usher_syndrome_type_1F|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1D|PCDH15-related_disorder": 1,
    "PCDH15-related_disorder|not_provided|not_specified|Usher_syndrome_type_1F": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F|not_specified": 3,
    "Usher_syndrome_type_1F|not_provided|not_specified": 7,
    "not_specified|Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive|not_provided|PCDH15-related_disorder|Usher_syndrome_type_1F": 1,
    "not_provided|Meniere_disease|Usher_syndrome_type_1F": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1F": 4,
    "Usher_syndrome_type_1F|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1F|not_specified|not_provided": 1,
    "not_provided|Usher_syndrome_type_1F|PCDH15-related_disorder": 2,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1F|Inborn_genetic_diseases|not_provided": 5,
    "Usher_syndrome_type_1F|not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided": 1,
    "not_provided|PCDH15-related_disorder|Usher_syndrome_type_1F": 2,
    "Usher_syndrome_type_1|not_specified|not_provided|Usher_syndrome_type_1F": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided|not_specified": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified|not_provided|Usher_syndrome_type_1": 2,
    "not_specified|not_provided|Usher_syndrome_type_1F": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_specified|not_provided|Usher_syndrome_type_1": 4,
    "not_provided|Usher_syndrome_type_1F|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1|not_provided|not_specified|Inborn_genetic_diseases|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1F|not_provided|Usher_syndrome_type_1|not_specified": 2,
    "PCDH15-related_disorder|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases": 7,
    "PCDH15-related_disorder|not_provided|Usher_syndrome_type_1F": 4,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_provided": 7,
    "not_provided|Usher_syndrome_type_1F|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23": 6,
    "Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|PCDH15-related_disorder|not_specified|not_provided": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided": 11,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1|not_provided|not_specified|Usher_syndrome_type_1F": 1,
    "not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 4,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome|Nonsyndromic_Deafness|not_provided": 1,
    "not_specified|PCDH15-related_disorder|not_provided|Usher_syndrome_type_1F": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23": 21,
    "not_provided|Usher_syndrome_type_1F|Usher_syndrome_type_1|PCDH15-related_disorder|not_specified": 1,
    "PCDH15-related_disorder|Usher_syndrome_type_1F|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|not_provided": 1,
    "Usher_syndrome_type_1F|not_provided|Inborn_genetic_diseases": 4,
    "Usher_syndrome_type_1F|not_provided|Usher_syndrome_type_1": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_provided": 4,
    "Usher_syndrome_type_1|Retinal_dystrophy": 1,
    "Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 6,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F|PCDH15-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_specified|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F": 1,
    "not_provided|Usher_syndrome_type_1F|Inborn_genetic_diseases": 10,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_specified|Usher_syndrome_type_1|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1F": 3,
    "not_provided|Usher_syndrome_type_1F|PCDH15-related_disorder|not_specified": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1F|not_provided|not_specified": 2,
    "not_specified|not_provided|Usher_syndrome_type_1F|Usher_syndrome_type_1": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided|Usher_syndrome_type_1F": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1F": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided": 8,
    "not_specified|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1F": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|Retinitis_pigmentosa-deafness_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_provided|not_specified": 1,
    "not_provided|Usher_syndrome_type_1|PCDH15-related_disorder": 2,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Rare_genetic_deafness": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1F": 2,
    "Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1F|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|PCDH15-related_disorder|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|Usher_syndrome|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided": 1,
    "not_provided|Usher_syndrome_type_1D": 8,
    "Inborn_genetic_diseases|Usher_syndrome_type_1F|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified": 1,
    "not_provided|not_specified|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Non-Syndromic_Hereditary_Hearing_Impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|Usher_syndrome_type_1D": 2,
    "not_specified|Usher_syndrome_type_1F|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "not_provided|Usher_syndrome_type_1F|not_specified|Inborn_genetic_diseases": 2,
    "PCDH15-related_disorder|not_provided|not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1F": 2,
    "Usher_syndrome_type_1F|not_specified|PCDH15-related_disorder|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F|Inborn_genetic_diseases": 1,
    "not_specified|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1F": 1,
    "not_specified|not_provided|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided|not_specified|Usher_syndrome_type_1F": 1,
    "Optic_atrophy|not_provided|PCDH15-related_disorder|not_specified|Usher_syndrome_type_1D|Usher_syndrome_type_1F": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1|not_provided|not_specified": 1,
    "PCDH15-related_disorder|not_specified|not_provided|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified|not_provided|Usher_syndrome_type_1|Hearing_impairment": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F|PCDH15-related_disorder": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|not_specified": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Inborn_genetic_diseases|not_provided": 2,
    "Optic_atrophy|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1F": 1,
    "not_provided|Usher_syndrome_type_1F|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|Usher_syndrome_type_1D|not_provided": 1,
    "not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 1,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|Rare_genetic_deafness": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_provided|Usher_syndrome_type_1F|not_specified": 1,
    "not_specified|PCDH15-related_disorder|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Childhood_onset_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_23|PCDH15-related_disorder|Retinal_dystrophy|Usher_syndrome_type_1F": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|Usher_syndrome_type_1D": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1F|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1D|not_specified|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|not_provided": 1,
    "Usher_syndrome_type_1F|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Inborn_genetic_diseases": 1,
    "not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1F|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome_type_1F": 1,
    "not_provided|Usher_syndrome_type_1F|Hearing_impairment": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome_type_1": 7,
    "not_provided|Usher_syndrome_type_1F|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|PCDH15-related_disorder": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1|not_provided|Retinal_dystrophy|not_specified": 1,
    "Usher_syndrome_type_1|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_provided|not_specified": 1,
    "not_specified|Usher_syndrome_type_1D|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1|not_provided": 1,
    "PCDH15-related_disorder|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1|not_provided|Hearing_impairment": 2,
    "PCDH15-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_provided|Usher_syndrome_type_1|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1F": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|PCDH15-related_disorder|not_specified|not_provided|Optic_atrophy": 1,
    "PCDH15-related_disorder|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1G": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_specified": 2,
    "not_provided|Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "not_specified|Usher_syndrome_type_1F|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Usher_syndrome_type_1F": 1,
    "not_specified|not_provided|Usher_syndrome_type_1F|Retinitis_pigmentosa|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases|not_specified|Usher_syndrome_type_1F": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1F|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1F|not_specified|not_provided": 2,
    "Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1G": 61,
    "PCDH15-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1F": 1,
    "Usher_syndrome_type_1F|PCDH15-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1F|Usher_syndrome_type_1D": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_23|not_specified|Usher_syndrome_type_1F": 1,
    "not_provided|Rare_genetic_deafness|USHER_SYNDROME|_TYPE_ID/F|_DIGENIC|Usher_syndrome_type_1|Usher_syndrome_type_1F": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1F": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D|Usher_syndrome_type_1F|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1F|Autosomal_recessive_nonsyndromic_hearing_loss_23|Usher_syndrome_type_1D": 1,
    "not_provided|TFAM-related_disorder": 1,
    "TFAM-related_disorder": 3,
    "TFAM-related_disorder|Mitochondrial_DNA_depletion_syndrome_15_(hepatocerebral_type)|not_provided": 1,
    "TFAM-related_disorder|not_provided": 1,
    "Renal_dysplasia|_cystic|_susceptibility_to": 87,
    "Renal_dysplasia|_cystic|_susceptibility_to|not_provided": 11,
    "not_provided|BICC1-related_disorder": 6,
    "not_provided|Renal_dysplasia|_cystic|_susceptibility_to|not_specified": 1,
    "not_provided|Renal_dysplasia|_cystic|_susceptibility_to": 9,
    "not_specified|not_provided|Renal_dysplasia|_cystic|_susceptibility_to": 3,
    "Renal_dysplasia|_cystic|_susceptibility_to|not_specified": 3,
    "not_provided|not_specified|Renal_dysplasia|_cystic|_susceptibility_to": 3,
    "not_specified|Renal_dysplasia|_cystic|_susceptibility_to": 5,
    "not_specified|BICC1-related_disorder|not_provided": 1,
    "BICC1-related_disorder|not_provided": 4,
    "not_specified|Renal_dysplasia|_cystic|_susceptibility_to|not_provided": 3,
    "BICC1-related_disorder|not_specified": 1,
    "BICC1-related_disorder": 1,
    "not_provided|not_specified|BICC1-related_disorder": 1,
    "not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome": 12,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided": 19,
    "ANK3-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "ANK3-related_disorder|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified|not_provided": 3,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome": 49,
    "ANK3-related_disorder|not_provided": 20,
    "ANK3-related_disorder|not_specified|not_provided": 8,
    "ANK3-related_disorder": 20,
    "ANK3-related_disorder|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome": 1,
    "not_provided|ANK3-related_disorder": 12,
    "Intellectual_disability|_autosomal_recessive_66": 15,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome": 3,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|ANK3-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome": 1,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|Inborn_genetic_diseases": 4,
    "ANK3-related_disorder|Inborn_genetic_diseases|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided|not_specified": 1,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|ANK3-related_disorder|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided": 2,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided|not_specified": 4,
    "not_specified|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided": 2,
    "not_provided|ANK3-related_disorder|not_specified": 5,
    "not_provided|not_specified|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome": 2,
    "Inborn_genetic_diseases|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|ANK3-related_disorder": 1,
    "Classic_medulloblastoma": 2,
    "not_specified|ANK3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided": 1,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|ANK3-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified": 1,
    "not_specified|ANK3-related_disorder|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_provided": 2,
    "not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|Autism|not_specified": 1,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|ANK3-related_disorder|not_provided": 1,
    "not_specified|not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|ANK3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|ANK3-related_disorder": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_66": 1,
    "not_specified|not_provided|ANK3-related_disorder": 2,
    "Intellectual_disability-hypotonia-spasticity-sleep_disorder_syndrome|not_specified": 1,
    "ANK3-related_neurodevelopmental_disorder": 2,
    "TMEM26-related_condition": 1,
    "ARID5B-related_disorder": 20,
    "not_provided|ARID5B-related_disorder": 1,
    "Blue_sclerae|Delayed_speech_and_language_development|Global_developmental_delay|Fetal_growth_restriction|Retrognathia|Pes_valgus|Prominent_forehead|Abnormality_of_mouth_size": 1,
    "ARID5B-related_disorder|not_provided": 1,
    "not_provided|Nephrolithiasis|_uric_acid|_susceptibility_to": 1,
    "Charcot-Marie-Tooth_disease_type_1D": 15,
    "Charcot-Marie-Tooth_disease_type_1D|not_provided": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_1D": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease_type_1D": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1D": 1,
    "Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|_type_I|Dejerine-sottas_neuropathy|_autosomal_dominant": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease_type_1D|ERG2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease_type_4E": 3,
    "Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease": 4,
    "Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1D|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_1D|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4E": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_1D|Dejerine-sottas_neuropathy|_autosomal_dominant|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease_type_1D|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease_type_1D": 1,
    "Charcot-Marie-Tooth_disease|_type_I|EGR2-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_1D|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 2,
    "not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease": 3,
    "not_provided|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 2,
    "EGR2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease_type_4E|Dejerine-Sottas_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I|EGR2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_1D|Dejerine-Sottas_disease|not_specified|Charcot-Marie-Tooth_disease_type_4E|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1D|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4E|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_disease_type_1D|Dejerine-Sottas_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_1D|Charcot-Marie-Tooth_disease|_type_I|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease_type_4E": 1,
    "JMJD1C-related_disorder": 9,
    "Early_myoclonic_encephalopathy|not_provided|JMJD1C-related_disorder": 2,
    "JMJD1C-related_disorder|Early_myoclonic_encephalopathy": 6,
    "JMJD1C-related_disorder|Early_myoclonic_encephalopathy|not_provided": 2,
    "not_provided|Early_myoclonic_encephalopathy|not_specified": 5,
    "Early_myoclonic_encephalopathy|JMJD1C-related_disorder": 14,
    "JMJD1C-associated_Neurodevelopmental_Disorder": 2,
    "Early_myoclonic_encephalopathy|Hepatoblastoma": 1,
    "Early_myoclonic_encephalopathy|not_specified|not_provided": 4,
    "JMJD1C-associated_Neurodevelopmental_Disorder|Early_myoclonic_encephalopathy": 2,
    "not_provided|not_specified|Early_myoclonic_encephalopathy": 2,
    "JMJD1C-related_disorder|Neurodevelopmental_disorder": 1,
    "not_provided|JMJD1C-related_disorder": 1,
    "not_provided|Early_myoclonic_encephalopathy|JMJD1C-related_disorder": 2,
    "JMJD1C-related_disorder|not_provided|Early_myoclonic_encephalopathy|not_specified": 1,
    "JMJD1C-related_Neurodevelopmental_disorder|Early_myoclonic_encephalopathy": 1,
    "Early_myoclonic_encephalopathy|JMJD1C-associated_Neurodevelopmental_Disorder": 1,
    "TELO2-related_intellectual_disability-neurodevelopmental_disorder": 14,
    "Early_myoclonic_encephalopathy|JMJD1C-related_disorder|not_provided": 1,
    "Benign_familial_infantile_epilepsy|Early_myoclonic_encephalopathy": 1,
    "not_provided|JMJD1C-related_disorder|Early_myoclonic_encephalopathy": 1,
    "JMJD1C-related_disorder|not_provided|Early_myoclonic_encephalopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13": 448,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_specified": 120,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_13": 85,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_provided": 14,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_specified|not_provided": 12,
    "Arrhythmogenic_right_ventricular_dysplasia_13|Left_ventricular_noncompaction_cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_13|Primary_dilated_cardiomyopathy|not_provided|CTNNA3-related_disorder": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_provided|not_specified": 10,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_13": 8,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_13": 5,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_13": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_specified|not_provided|CTNNA3-related_disorder": 2,
    "CTNNA3-related_disorder": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_13|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "CTNNA3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_13": 4,
    "CTNNA3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_13|not_specified": 3,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_13|CTNNA3-related_disorder|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_13|not_specified": 9,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_13|CTNNA3-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_13": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_13|Congenital_heart_disease": 2,
    "CTNNA3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_13|not_specified|not_provided": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_13|not_provided": 7,
    "Congenital_heart_disease|Arrhythmogenic_right_ventricular_dysplasia_13": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_specified|CTNNA3-related_disorder": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_provided|CTNNA3-related_disorder": 1,
    "not_provided|CTNNA3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_13|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_13|CTNNA3-related_disorder|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Congenital_heart_disease|not_specified": 1,
    "not_specified|CTNNA3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_13": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_13|CTNNA3-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|CTNNA3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_13": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|CTNNA3-related_disorder": 1,
    "Long_QT_syndrome|Arrhythmogenic_right_ventricular_dysplasia_13": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_13|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_13|Congenital_heart_disease": 1,
    "Hyperphenylalaninemia_due_to_DNAJC12_deficiency": 11,
    "DNAJC12-related_disorder|Hyperphenylalaninemia_due_to_DNAJC12_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Hyperphenylalaninemia_due_to_DNAJC12_deficiency|not_provided": 4,
    "not_provided|Hyperphenylalaninemia_due_to_DNAJC12_deficiency": 2,
    "DNAJC12-related_disorder|not_provided": 4,
    "SIRT1-related_disorder|not_provided": 7,
    "SIRT1-related_disorder": 1,
    "not_provided|SIRT1-related_disorder": 1,
    "not_specified|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK": 2,
    "Dilated_cardiomyopathy_1KK": 532,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 139,
    "Dilated_cardiomyopathy_1KK|not_provided": 26,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 73,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 17,
    "MYPN-related_myopathy": 11,
    "not_provided|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Familial_hypertrophic_cardiomyopathy_22|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 8,
    "not_provided|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 14,
    "Dilated_cardiomyopathy_1KK|not_specified|Cardiovascular_phenotype": 6,
    "MYPN-related_disorder": 8,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Cardiovascular_phenotype": 5,
    "not_provided|Dilated_cardiomyopathy_1KK": 18,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided": 21,
    "not_provided|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy": 4,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy": 2,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_provided": 2,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy": 15,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1KK|not_provided|MYPN-related_myopathy|Cardiovascular_phenotype|MYPN-related_disorder": 1,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|MYPN-related_myopathy": 5,
    "Long_QT_syndrome|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 6,
    "Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|Primary_dilated_cardiomyopathy|MYPN-related_myopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|MYPN-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|MYPN-related_disorder": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK": 5,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1KK": 16,
    "Dilated_cardiomyopathy_1KK|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYPN-related_disorder|Dilated_cardiomyopathy_1KK|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_specified": 2,
    "MYPN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 2,
    "MYPN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 3,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_provided": 7,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|Cardiovascular_phenotype": 13,
    "Dilated_cardiomyopathy_1KK|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|not_specified|not_provided": 5,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_provided|not_specified|MYPN-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_specified": 4,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_provided|MYPN-related_myopathy": 2,
    "not_provided|MYPN-related_disorder|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|MYPN-related_disorder|Dilated_cardiomyopathy_1KK": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Restrictive_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK": 2,
    "Cardiovascular_phenotype|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 3,
    "not_provided|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided": 3,
    "not_specified|Dilated_cardiomyopathy_1KK|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy": 11,
    "not_specified|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 4,
    "not_provided|Dilated_cardiomyopathy_1KK|not_specified|MYPN-related_myopathy|Cardiovascular_phenotype": 1,
    "MYPN-related_disorder|Dilated_cardiomyopathy_1KK": 2,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_specified|Cardiovascular_phenotype|Left_ventricular_hypertrophy|Left_ventricular_noncompaction_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|not_specified|not_provided|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1KK|not_specified": 12,
    "not_provided|not_specified|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy": 1,
    "Dilated_cardiomyopathy_1KK|Dilated_cardiomyopathy_1A|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1KK|not_specified": 1,
    "MYPN-related_myopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|not_specified": 4,
    "not_provided|Cardiovascular_phenotype|MYPN-related_disorder|Dilated_cardiomyopathy_1KK": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1KK": 3,
    "not_specified|Dilated_cardiomyopathy_1KK": 7,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1KK|not_provided": 4,
    "not_provided|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|MYPN-related_disorder|not_specified|Dilated_cardiomyopathy_1KK|not_provided": 2,
    "Congenital_myopathy|Dilated_cardiomyopathy_1KK": 1,
    "MYPN-related_disorder|Dilated_cardiomyopathy_1KK|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|MYPN-related_disorder": 1,
    "not_specified|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided": 1,
    "MYPN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|MYPN-related_myopathy": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1KK": 1,
    "Cardiomyopathy|_familial_restrictive|_4|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1KK": 2,
    "Dilated_cardiomyopathy_1KK|not_provided|MYPN-related_disorder|Cardiovascular_phenotype": 2,
    "MYPN-related_myopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1KK|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy": 4,
    "MYPN-related_myopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified|not_provided|MYPN-related_disorder": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|MYPN-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1KK|not_specified": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_provided|Cardiovascular_phenotype": 4,
    "not_provided|MYPN-related_disorder|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_provided": 2,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|not_specified|MYPN-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|MYPN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified": 1,
    "MYPN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1KK|See_cases": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 3,
    "not_provided|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK": 1,
    "MYPN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYPN-related_disorder|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|MYPN-related_disorder|not_specified|Dilated_cardiomyopathy_1KK|not_provided|See_cases": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1KK|MYPN-related_disorder|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|Left_ventricular_noncompaction_1": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|Primary_dilated_cardiomyopathy|MYPN-related_myopathy|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_provided": 2,
    "Dilated_cardiomyopathy_1KK|not_provided|MYPN-related_myopathy|not_specified": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_specified": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "MYPN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Cap_myopathy": 1,
    "MYPN-related_disorder|Cardiovascular_phenotype": 4,
    "not_provided|Dilated_cardiomyopathy_1KK|not_specified": 2,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|Sudden_unexplained_death": 1,
    "not_provided|Dilated_cardiomyopathy_1KK|not_specified|Cardiovascular_phenotype": 1,
    "MYPN-related_myopathy|not_specified|Dilated_cardiomyopathy_1KK|not_provided": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|not_specified|MYPN-related_myopathy": 1,
    "Cardiovascular_phenotype|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Cardiomyopathy|MYPN-related_myopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1KK|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|MYPN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "MYPN-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1KK": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_disorder": 1,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYPN-related_disorder": 1,
    "not_provided|MYPN-related_myopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 1,
    "Dilated_cardiomyopathy_1KK|not_provided|MYPN-related_disorder|MYPN-related_myopathy|Cardiovascular_phenotype": 1,
    "MYPN-related_myopathy|not_provided|Dilated_cardiomyopathy_1KK": 1,
    "MYPN-related_disorder|not_specified|Dilated_cardiomyopathy_1KK|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Familial_hypertrophic_cardiomyopathy_22|Dilated_cardiomyopathy_1KK|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified": 2,
    "MYPN-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK": 1,
    "MYPN-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|MYPN-related_disorder|MYPN-related_myopathy": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Heart_failure|Cardiomyopathy|Primary_dilated_cardiomyopathy|Primary_familial_dilated_cardiomyopathy|not_provided|not_specified|Dilated_cardiomyopathy_1KK": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1KK": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1KK|not_provided": 1,
    "MYPN-related_disorder|Cardiovascular_phenotype|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|not_specified|not_provided": 1,
    "MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1A": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1KK|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1KK|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1KK|not_specified|Cardiovascular_phenotype|not_provided|MYPN-related_myopathy": 1,
    "MYPN-related_disorder|Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|MYPN-related_myopathy|Dilated_cardiomyopathy_1KK": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1KK|MYPN-related_myopathy|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1KK|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Optic_nerve_hypoplasia|Foveal_hypoplasia|not_provided": 1,
    "Optic_nerve_hypoplasia|Foveal_hypoplasia": 1,
    "not_provided|not_specified|ATOH7-related_condition": 1,
    "Persistent_hyperplastic_primary_vitreous|_autosomal_recessive": 4,
    "ATOH7-related_condition|not_provided": 1,
    "not_provided|Persistent_hyperplastic_primary_vitreous|_autosomal_recessive": 1,
    "Rothmund-Thomson_syndrome|Rothmund-Thomson_syndrome_type_4": 2,
    "Ateleiotic_dwarfism|Seckel_syndrome_8": 1,
    "Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy": 8,
    "DNA2-related_disorder|not_provided": 6,
    "not_provided|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Seckel_syndrome_8": 2,
    "DNA2-related_disorder|Microcephaly|not_provided": 1,
    "not_provided|DNA2-related_disorder": 8,
    "Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Seckel_syndrome_8|not_provided|not_specified": 1,
    "DNA2-related_disorder": 5,
    "DNA2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|DNA2-related_disorder": 3,
    "Seckel_syndrome_8": 2,
    "Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|not_provided": 4,
    "not_specified|not_provided|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Inborn_genetic_diseases": 1,
    "not_provided|Rothmund-Thomson_syndrome_type_4|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Seckel_syndrome_8": 1,
    "DNA2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Rothmund-Thomson_syndrome|Rothmund-Thomson_syndrome_type_4|not_provided": 1,
    "not_provided|DNA2-related_disorder|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Seckel_syndrome_8": 1,
    "not_provided|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy": 5,
    "Seckel_syndrome_8|not_provided": 1,
    "not_provided|Seckel_syndrome_8|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|not_specified": 1,
    "Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Seckel_syndrome_8|not_provided": 1,
    "Seckel_syndrome_8|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy": 1,
    "Rothmund-Thomson_syndrome_type_4|Rothmund-Thomson_syndrome": 3,
    "not_provided|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|not_specified|Seckel_syndrome_8": 1,
    "DNA2-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|DNA2-related_disorder|Mitochondrial_DNA_deletion_syndrome_with_progressive_myopathy|Seckel_syndrome_8": 1,
    "not_provided|Seckel_syndrome_8": 1,
    "autosomal_recessive_isolated_fingernail_dysplasia|not_provided|Inherited_isolated_nail_anomaly": 1,
    "TET1-related_disorder": 14,
    "TET1-related_disorder|not_provided": 5,
    "not_provided|TET1-related_disorder": 2,
    "Hypothyroidism|Hearing_impairment|Neurodevelopmental_delay": 1,
    "Preeclampsia/eclampsia_4": 3,
    "STOX1-related_disorder": 4,
    "not_specified|Preeclampsia/eclampsia_4": 1,
    "Cytosolic_phospholipase-A2_alpha_deficiency_associated_bleeding_disorder|not_specified|not_provided|Preeclampsia/eclampsia_4": 1,
    "not_specified|STOX1-related_disorder": 1,
    "Goldberg-Shprintzen_syndrome|not_provided": 5,
    "Goldberg-Shprintzen_syndrome": 42,
    "KIFBP-related_disorder|not_specified|not_provided|Goldberg-Shprintzen_syndrome": 1,
    "not_provided|not_specified|Goldberg-Shprintzen_syndrome|KIFBP-related_disorder": 1,
    "not_specified|Goldberg-Shprintzen_syndrome|not_provided": 3,
    "not_specified|Goldberg-Shprintzen_syndrome": 2,
    "not_provided|not_specified|Goldberg-Shprintzen_syndrome": 1,
    "not_provided|Goldberg-Shprintzen_syndrome": 3,
    "not_provided|KIFBP-related_disorder|not_specified|Goldberg-Shprintzen_syndrome": 1,
    "Goldberg-Shprintzen_syndrome|not_specified": 2,
    "Goldberg-Shprintzen_syndrome|not_provided|not_specified": 1,
    "not_provided|Goldberg-Shprintzen_syndrome|not_specified": 2,
    "KIFBP-related_disorder|not_provided": 1,
    "not_specified|not_provided|Goldberg-Shprintzen_syndrome": 3,
    "not_provided|KIFBP-related_disorder|Goldberg-Shprintzen_syndrome": 1,
    "Goldberg-Shprintzen_syndrome|not_specified|not_provided": 1,
    "Epilepsy|not_specified": 1,
    "Retinitis_pigmentosa_92": 7,
    "not_provided|Keratoconus_1": 3,
    "Nonsyndromic_cleft_lip_palate|Retinitis_pigmentosa_92": 1,
    "Retinitis_pigmentosa_92|not_specified": 1,
    "Nonsyndromic_cleft_lip_palate": 4,
    "HK1-related_disorder": 10,
    "Charcot-Marie-Tooth_disease_type_4G": 4,
    "not_provided|Charcot-Marie-Tooth_disease_type_4G|Hemolytic_anemia_due_to_hexokinase_deficiency": 1,
    "Hemolytic_anemia_due_to_hexokinase_deficiency": 5,
    "Charcot-Marie-Tooth_disease_type_4G|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies": 1,
    "HK1-related_disorder|not_provided": 10,
    "not_specified|HK1-related_disorder|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4G|Hemolytic_anemia_due_to_hexokinase_deficiency|Retinitis_pigmentosa_79|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|HK1-related_disorder": 1,
    "Retinitis_pigmentosa_79|Hemolytic_anemia_due_to_hexokinase_deficiency|Charcot-Marie-Tooth_disease_type_4G|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided": 1,
    "not_provided|HK1-related_disorder": 8,
    "Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided|Charcot-Marie-Tooth_disease_type_4G|Retinitis_pigmentosa_79|Retinal_dystrophy|not_specified|Hemolytic_anemia_due_to_hexokinase_deficiency": 1,
    "Hemolytic_anemia_due_to_hexokinase_deficiency|HK1-related_disorder|not_provided": 1,
    "not_provided|Hemolytic_anemia_due_to_hexokinase_deficiency": 2,
    "Hemolytic_anemia_due_to_hexokinase_deficiency|not_provided": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_79|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided|Hemolytic_anemia_due_to_hexokinase_deficiency|Charcot-Marie-Tooth_disease_type_4G": 1,
    "Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies": 10,
    "not_provided|Charcot-Marie-Tooth_disease_type_4G": 2,
    "HK1-related_disorder|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_79": 2,
    "HK1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4G|Hemolytic_anemia_due_to_hexokinase_deficiency|Retinitis_pigmentosa_79|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided": 2,
    "not_specified|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_79|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Hemolytic_anemia_due_to_hexokinase_deficiency|Charcot-Marie-Tooth_disease_type_4G|not_provided": 1,
    "Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_delay|not_provided|Retinitis_pigmentosa_79|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies": 1,
    "Charcot-Marie-Tooth_disease_type_4G|Neurodevelopmental_abnormality|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies": 1,
    "not_provided|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies": 4,
    "Retinitis_pigmentosa_79|not_provided": 1,
    "Retinitis_pigmentosa_79|Retinal_dystrophy|Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided|Autism_spectrum_disorder|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Hemolytic_anemia_due_to_hexokinase_deficiency": 1,
    "Retinitis_pigmentosa_79|Charcot-Marie-Tooth_disease_type_4G|Hemolytic_anemia_due_to_hexokinase_deficiency|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|HK1-related_disorder|not_provided": 2,
    "Retinal_dystrophy|Charcot-Marie-Tooth_disease_type_4G|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Retinitis_pigmentosa_79|Hemolytic_anemia_due_to_hexokinase_deficiency|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4G|Hemolytic_anemia_due_to_hexokinase_deficiency|Retinitis_pigmentosa_79|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided": 1,
    "Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|Charcot-Marie-Tooth_disease_type_4G|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4G|Retinitis_pigmentosa_79|Hemolytic_anemia_due_to_hexokinase_deficiency|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|not_provided": 2,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies": 1,
    "not_provided|Neurodevelopmental_disorder_with_visual_defects_and_brain_anomalies|HK1-related_disorder": 1,
    "Hemolytic_anemia_due_to_hexokinase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Macular_dystrophy": 1,
    "HK1-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_79|See_cases": 1,
    "not_provided|Retinal_dystrophy|HK1-related_disorder": 1,
    "not_provided|not_specified|Congenital_malabsorptive_diarrhea_4": 1,
    "not_provided|Congenital_malabsorptive_diarrhea_4": 2,
    "Congenital_malabsorptive_diarrhea_4": 6,
    "Congenital_malabsorptive_diarrhea_4|not_provided": 4,
    "Congenital_malabsorptive_diarrhea_4|Inborn_genetic_diseases": 1,
    "Congenital_malabsorptive_diarrhea_4|NEUROG3-related_disorder": 1,
    "NEUROG3-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|NEUROG3-related_disorder|Congenital_malabsorptive_diarrhea_4": 1,
    "not_provided|COL13A1-related_disorder": 10,
    "COL13A1-related_disorder": 7,
    "not_provided|Congenital_myasthenic_syndrome_19|Inborn_genetic_diseases": 5,
    "not_provided|Congenital_myasthenic_syndrome_19": 12,
    "Congenital_myasthenic_syndrome_19|not_provided": 9,
    "COL13A1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "COL13A1-related_disorder|not_provided": 18,
    "Congenital_myasthenic_syndrome_19": 28,
    "Congenital_myasthenic_syndrome_19|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_19": 2,
    "Congenital_myasthenic_syndrome_19|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_19|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|COL13A1-related_disorder": 1,
    "Inborn_genetic_diseases|COL13A1-related_disorder|not_provided": 1,
    "Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal": 10,
    "Heterotaxy|_visceral|_5|_autosomal|Holoprosencephaly_sequence": 22,
    "Holoprosencephaly_sequence|Visceral_heterotaxy": 1,
    "Holoprosencephaly_sequence|not_provided|Heterotaxy|_visceral|_5|_autosomal": 4,
    "Heterotaxy|_visceral|_5|_autosomal": 49,
    "Basal_cell_carcinoma|_susceptibility_to|_4": 1,
    "Inborn_genetic_diseases|Heterotaxy|_visceral|_5|_autosomal": 2,
    "Heterotaxy|_visceral|_5|_autosomal|NODAL-related_disorder|Holoprosencephaly_sequence": 1,
    "Heterotaxy|_visceral|_5|_autosomal|Inborn_genetic_diseases|not_provided": 1,
    "NODAL-related_disorder|not_provided": 1,
    "not_provided|Heterotaxy|_visceral|_5|_autosomal": 4,
    "Heterotaxy|_visceral|_5|_autosomal|NODAL-related_disorder": 3,
    "not_specified|not_provided|Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal": 1,
    "NODAL-related_disorder": 4,
    "NODAL-related_disorder|Inborn_genetic_diseases|not_provided|Visceral_heterotaxy|Heterotaxy|_visceral|_5|_autosomal|Wolff-Parkinson-White_pattern": 1,
    "Heterotaxy|_visceral|_5|_autosomal|NODAL-related_disorder|not_provided": 1,
    "Heterotaxy|_visceral|_5|_autosomal|Inborn_genetic_diseases": 5,
    "Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal|not_specified": 1,
    "Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal|Inborn_genetic_diseases": 1,
    "Heterotaxy|_visceral|_5|_autosomal|not_specified|Holoprosencephaly_sequence|not_provided": 1,
    "not_specified|Heterotaxy|_visceral|_5|_autosomal|Inborn_genetic_diseases|not_provided": 1,
    "Congenitally_corrected_transposition_of_the_great_arteries|not_provided": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal": 1,
    "Heterotaxy|_visceral|_5|_autosomal|not_specified": 1,
    "NODAL-related_disorder|not_specified|not_provided|Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal": 1,
    "Holoprosencephaly_sequence|not_provided|NODAL-related_disorder|Heterotaxy|_visceral|_5|_autosomal": 1,
    "not_provided|Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal": 1,
    "Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal|not_provided|not_specified": 1,
    "Holoprosencephaly_sequence|Heterotaxy|_visceral|_5|_autosomal|not_provided": 1,
    "NODAL-related_disorder|Heterotaxy|_visceral|_5|_autosomal": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2": 407,
    "Familial_hemophagocytic_lymphohistiocytosis|not_provided|not_specified": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 13,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_provided": 11,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia": 14,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Familial_hemophagocytic_lymphohistiocytosis|Lymphoma|_non-Hodgkin|_familial": 3,
    "not_provided|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Inborn_genetic_diseases": 15,
    "Lymphoma|_non-Hodgkin|_familial|PRF1-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia": 4,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2": 10,
    "Familial_hemophagocytic_lymphohistiocytosis_2|PRF1-related_disorder|Familial_hemophagocytic_lymphohistiocytosis|not_provided|Aplastic_anemia": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_2": 11,
    "Inborn_genetic_diseases|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 2,
    "PRF1-related_disorder|Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2": 5,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|not_provided": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial": 2,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|not_provided": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|not_specified|not_provided": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_2": 2,
    "Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "PRF1-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_2": 8,
    "Familial_hemophagocytic_lymphohistiocytosis_2|PRF1-related_disorder": 5,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|not_provided": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial": 10,
    "Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|PRF1-related_disorder": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_2": 11,
    "Aplastic_anemia|not_specified": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Inborn_genetic_diseases|Aplastic_anemia": 1,
    "PRF1-related_disorder|not_specified|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_specified": 6,
    "not_specified|Aplastic_anemia|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia": 2,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|not_specified": 2,
    "Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_2": 3,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_provided|Inborn_genetic_diseases": 1,
    "Aplastic_anemia|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis|Autoinflammatory_syndrome": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|PRF1-related_disorder": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial": 1,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 2,
    "Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "not_specified|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|Inborn_genetic_diseases": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_provided|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|not_provided": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Familial_hemophagocytic_lymphohistiocytosis": 2,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome": 2,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|not_provided": 1,
    "Lymphoma|_non-Hodgkin|_familial|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "PRF1-related_disorder": 2,
    "Familial_hemophagocytic_lymphohistiocytosis|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2": 2,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Autoinflammatory_syndrome|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|PRF1-related_disorder|Inborn_genetic_diseases": 1,
    "Lymphoma|_non-Hodgkin|_familial|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|not_provided": 1,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_type_1|Familial_hemophagocytic_lymphohistiocytosis_2|Familial_hemophagocytic_lymphohistiocytosis|Inborn_genetic_diseases|Aplastic_anemia": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 1,
    "Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Autoinflammatory_syndrome|not_provided|Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_specified|Inborn_genetic_diseases": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_specified|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|not_specified|not_provided": 2,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|not_provided|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2|Familial_hemophagocytic_lymphohistiocytosis|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial": 1,
    "not_provided|Autoinflammatory_syndrome|Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|not_specified|Lymphoma|_non-Hodgkin|_familial|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|not_provided|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|not_provided|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis|not_provided|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|not_provided|Autoinflammatory_syndrome|not_specified|PRF1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "PRF1-related_disorder|Autoinflammatory_syndrome|not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|Hemophagocytic_lymphohistiocytosis|_familial|_2|_susceptibility_to|not_provided": 1,
    "PRF1-related_disorder|not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia": 1,
    "Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Pelizaeus-Merzbacher_disease": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|not_provided|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|Lymphoma|_non-Hodgkin|_familial|Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "not_provided|Aplastic_anemia|PRF1-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "not_provided|Autoinflammatory_syndrome|not_specified|Familial_hemophagocytic_lymphohistiocytosis_2": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|PRF1-related_disorder|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|not_specified|PRF1-related_disorder|not_provided": 1,
    "not_specified|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|Familial_hemophagocytic_lymphohistiocytosis_2|Autoinflammatory_syndrome|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial|Autoinflammatory_syndrome|PRF1-related_disorder|Familial_hemophagocytic_lymphohistiocytosis|not_provided": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_2|See_cases|PRF1-related_disorder": 1,
    "not_specified|Aplastic_anemia|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_2|not_provided": 1,
    "not_specified|PRF1-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_2|Aplastic_anemia|Lymphoma|_non-Hodgkin|_familial": 1,
    "Aplastic_anemia|Familial_hemophagocytic_lymphohistiocytosis_2|Lymphoma|_non-Hodgkin|_familial|not_provided|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "Nephrotic_syndrome_14": 17,
    "Nephrotic_syndrome_14|not_provided": 9,
    "not_provided|SGPL1-related_disorder": 5,
    "Inborn_genetic_diseases|Nephrotic_syndrome_14": 2,
    "not_provided|Nephrotic_syndrome_14": 2,
    "SGPL1-related_disorder|not_provided": 4,
    "Nephrotic_syndrome_14|Nephrotic_syndrome|not_provided": 1,
    "SGPL1-related_disorder": 2,
    "Nephrotic_syndrome|Nephrotic_syndrome_14": 1,
    "not_provided|Inborn_genetic_diseases|Nephrotic_syndrome_14": 1,
    "not_provided|Pterin-4_alpha-carbinolamine_dehydratase_1_deficiency": 5,
    "Pterin-4_alpha-carbinolamine_dehydratase_1_deficiency": 97,
    "Pterin-4_alpha-carbinolamine_dehydratase_1_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|Pterin-4_alpha-carbinolamine_dehydratase_1_deficiency|PCBD1-related_disorder": 1,
    "Inborn_genetic_diseases|Pterin-4_alpha-carbinolamine_dehydratase_1_deficiency": 3,
    "Pterin-4_alpha-carbinolamine_dehydratase_1_deficiency|Inborn_genetic_diseases": 1,
    "UNC5B-related_disorder": 4,
    "not_specified|not_provided|H_syndrome": 2,
    "H_syndrome": 372,
    "Inborn_genetic_diseases|H_syndrome": 15,
    "not_specified|H_syndrome|not_provided": 2,
    "not_provided|H_syndrome": 24,
    "H_syndrome|not_provided|not_specified": 1,
    "H_syndrome|Inborn_genetic_diseases": 19,
    "SLC29A3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|H_syndrome": 1,
    "H_syndrome|SLC29A3-related_disorder": 5,
    "H_syndrome|not_provided": 12,
    "H_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Dysosteosclerosis|H_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|H_syndrome": 2,
    "SLC29A3-related_disorder": 1,
    "not_provided|H_syndrome|SLC29A3-related_disorder": 2,
    "H_syndrome|not_specified|not_provided": 8,
    "not_provided|Acanthosis_nigricans|not_specified|Gemcitabine_response|H_syndrome": 1,
    "SLC29A3-related_disorder|Inborn_genetic_diseases|H_syndrome": 1,
    "Inborn_genetic_diseases|H_syndrome|not_provided": 2,
    "SLC29A3-related_disorder|H_syndrome|not_provided": 1,
    "not_specified|H_syndrome": 1,
    "not_provided|H_syndrome|not_specified": 2,
    "SLC29A3-related_disorder|not_provided|H_syndrome": 1,
    "H_syndrome|SLC29A3-related_disorder|not_provided": 1,
    "SLC29A3-related_disorder|not_specified|not_provided|H_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 27,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|CDH23-related_disorder": 8,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 8,
    "Retinitis_pigmentosa-deafness_syndrome|CDH23-related_disorder|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "Retinitis_pigmentosa-deafness_syndrome|CDH23-related_disorder|Hearing_loss|_autosomal_recessive": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 13,
    "not_specified|not_provided|Retinitis_pigmentosa-deafness_syndrome|CDH23-related_disorder|Hearing_loss|_autosomal_recessive": 1,
    "Hearing_loss|_autosomal_recessive|not_specified|Retinitis_pigmentosa-deafness_syndrome|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|CDH23-related_disorder": 1,
    "not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 15,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified": 4,
    "not_specified|Usher_syndrome_type_1D|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 2,
    "Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 12,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 2,
    "Pituitary_adenoma_5|_multiple_types": 86,
    "not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 20,
    "not_specified|not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1|not_provided": 1,
    "not_specified|CDH23-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12": 99,
    "not_specified|Usher_syndrome_type_1|not_provided": 13,
    "not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 1,
    "not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 10,
    "Usher_syndrome_type_1D|Prelingual_sensorineural_hearing_impairment|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1": 1,
    "Inborn_genetic_diseases|CDH23-related_disorder|Usher_syndrome_type_1|not_provided": 1,
    "not_specified|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 4,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1|USHER_SYNDROME|_TYPE_ID/F|_DIGENIC": 1,
    "Usher_syndrome_type_1D|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 2,
    "not_provided|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 2,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|not_provided": 9,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|not_specified|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "Retinal_dystrophy|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "Childhood_onset_hearing_loss|not_provided|Usher_syndrome_type_1D": 1,
    "Pituitary_adenoma_5|_multiple_types|not_provided": 27,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D": 25,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|CDH23-related_disorder|not_provided": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 14,
    "Usher_syndrome_type_1|not_provided|not_specified": 12,
    "not_provided|Usher_syndrome_type_1|CDH23-related_disorder": 5,
    "not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types": 2,
    "Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome|Pituitary_adenoma_5|_multiple_types|Rare_genetic_deafness": 1,
    "not_provided|CDH23-related_disorder|Inborn_genetic_diseases|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|not_provided|CDH23-related_disorder": 6,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_specified|not_provided|Usher_syndrome_type_1": 3,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Retinitis_pigmentosa|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|Usher_syndrome_type_1D": 1,
    "not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified": 4,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_loss|_autosomal_recessive|not_provided|Retinitis_pigmentosa-deafness_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Usher_syndrome_type_1|not_provided": 3,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Pituitary_adenoma_5|_multiple_types": 27,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 14,
    "not_specified|Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 3,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 3,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1D": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1D": 10,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1|Nonsyndromic_genetic_hearing_loss": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided": 7,
    "not_provided|CDH23-related_disorder": 17,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided": 5,
    "not_provided|Usher_syndrome|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1": 10,
    "CDH23-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|not_specified": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome|Pituitary_adenoma_5|_multiple_types|Retinal_dystrophy|not_provided": 1,
    "not_provided|Rare_genetic_deafness|Pituitary_adenoma_5|_multiple_types": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 3,
    "CDH23-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided": 3,
    "Retinal_dystrophy|Nonsyndromic_genetic_hearing_loss|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Hearing_impairment|Retinal_dystrophy": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|not_provided": 1,
    "not_specified|CDH23-related_disorder|not_provided": 4,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 8,
    "not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome": 1,
    "CDH23-related_disorder|not_specified|not_provided": 6,
    "not_specified|not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Retinal_dystrophy|not_provided": 1,
    "CDH23-related_disorder|not_provided|not_specified": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1": 2,
    "Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1": 7,
    "not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "not_specified|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Neurodevelopmental_abnormality": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Rare_genetic_deafness|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 11,
    "Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1D|Inborn_genetic_diseases": 1,
    "not_specified|Usher_syndrome_type_1|not_provided|CDH23-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided": 3,
    "not_provided|not_specified|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|Retinitis_pigmentosa-deafness_syndrome|not_specified": 1,
    "Usher_syndrome_type_1D|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|not_specified|not_provided": 3,
    "not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 2,
    "not_provided|Usher_syndrome|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Usher_syndrome_type_1|not_specified|Nonsyndromic_genetic_hearing_loss": 1,
    "CDH23-related_disorder|not_specified|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 3,
    "Usher_syndrome_type_1|Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|Usher_syndrome_type_1D": 1,
    "not_specified|not_provided|CDH23-related_disorder": 3,
    "Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive|not_provided|not_specified|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases": 14,
    "not_specified|Usher_syndrome_type_1": 6,
    "Retinal_dystrophy|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Inborn_genetic_diseases|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified": 1,
    "not_provided|not_specified|CDH23-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1": 8,
    "CDH23-related_disorder|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|not_provided|Usher_syndrome_type_1D|Inborn_genetic_diseases": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 2,
    "not_specified|CDH23-related_disorder|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome|Usher_syndrome_type_1": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 2,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|not_provided|Usher_syndrome_type_1D": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1": 1,
    "not_provided|not_specified|Usher_syndrome_type_1D|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Rare_genetic_deafness": 1,
    "CDH23-related_disorder": 12,
    "CDH23-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1": 3,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 8,
    "CDH23-related_disorder|Usher_syndrome_type_1|not_provided|Rare_genetic_deafness": 1,
    "not_provided|not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 3,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Hearing_impairment|not_provided|Retinal_dystrophy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|not_provided|Usher_syndrome_type_1D": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|not_specified|CDH23-related_disorder": 2,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|not_provided|Usher_syndrome_type_1": 5,
    "CDH23-related_disorder|Pituitary_adenoma_5|_multiple_types|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 3,
    "Non-Syndromic_Hereditary_Hearing_Impairment|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Usher_syndrome_type_1|Retinitis_pigmentosa|Retinitis_pigmentosa-deafness_syndrome": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Rare_genetic_deafness|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|not_provided|CDH23-related_disorder|Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "not_provided|Hearing_impairment|Bilateral_sensorineural_hearing_impairment": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1|Usher_syndrome_type_1D|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Retinal_dystrophy|not_provided": 1,
    "Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1D": 1,
    "not_provided|Childhood_onset_hearing_loss|Usher_syndrome_type_1": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1": 2,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|VATER_association|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "CDH23-related_disorder|not_provided": 9,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|not_specified": 2,
    "not_provided|Retinitis_pigmentosa|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|CDH23-related_disorder|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1|not_provided": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 6,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 4,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Sensorineural_hearing_loss_disorder|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Ear_malformation": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|not_provided|Usher_syndrome_type_1D|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1|not_provided|not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1D|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|Usher_syndrome_type_1|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|not_provided|Cone-rod_dystrophy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified|not_provided": 3,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 2,
    "Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Hearing_loss|_autosomal_recessive|not_provided|Usher_syndrome_type_1|Usher_syndrome": 1,
    "not_provided|not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 6,
    "CDH23-related_disorder|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome|Rare_genetic_deafness|not_provided|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "Childhood_onset_hearing_loss|CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|not_specified": 7,
    "Hearing_loss|_autosomal_recessive|Retinitis_pigmentosa-deafness_syndrome": 1,
    "not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|not_provided": 2,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D": 1,
    "not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 1,
    "Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_impairment|Retinal_dystrophy": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1D": 1,
    "CDH23-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Retinitis_pigmentosa-deafness_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|CDH23-related_disorder": 1,
    "Retinal_dystrophy|not_specified|Usher_syndrome_type_1|not_provided": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified": 1,
    "Usher_syndrome_type_1|Cone-rod_dystrophy|not_specified|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 2,
    "Pituitary_adenoma_5|_multiple_types|Rare_genetic_deafness|not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Inborn_genetic_diseases|not_provided": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 3,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 3,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome|not_provided|not_specified|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome": 1,
    "Pituitary_adenoma_5|_multiple_types|Rare_genetic_deafness|not_provided": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|Retinal_dystrophy|not_provided|not_specified": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Hearing_loss|_autosomal_recessive": 1,
    "Meniere_disease|not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1D": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome|not_provided|not_specified|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 4,
    "Usher_syndrome|Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Intellectual_disability": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Retinitis_pigmentosa-deafness_syndrome|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 4,
    "Usher_syndrome_type_1|CDH23-related_disorder|not_provided": 3,
    "not_specified|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided": 3,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_84A|Usher_syndrome_type_1D|Inborn_genetic_diseases|not_provided": 1,
    "Usher_syndrome_type_1D|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Monogenic_hearing_loss|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided|not_specified": 1,
    "not_specified|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinal_dystrophy": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 3,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1D": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Ear_malformation|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|not_provided|not_specified|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1|Retinitis_pigmentosa-deafness_syndrome|not_specified|not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Pituitary_adenoma_5|_multiple_types|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1|not_provided|Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "not_provided|CDH23-related_disorder|Usher_syndrome_type_1": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|CDH23-related_disorder": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|not_specified": 1,
    "Retinitis_pigmentosa-deafness_syndrome|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|not_provided|not_specified|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "not_provided|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 4,
    "not_provided|Usher_syndrome|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "Inborn_genetic_diseases|CDH23-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D": 1,
    "Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Childhood_onset_hearing_loss|Rare_genetic_deafness|Usher_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|not_provided|CDH23-related_disorder|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Rare_genetic_deafness": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome|not_provided": 1,
    "not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "not_provided|Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "not_provided|not_specified|CDH23-related_disorder|Usher_syndrome_type_1D|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "Childhood_onset_hearing_loss|not_specified|not_provided": 3,
    "not_provided|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Optic_atrophy|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|CDH23-related_disorder": 1,
    "not_specified|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Beta-D-mannosidosis|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|not_provided|CDH23-related_disorder|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|Pituitary_adenoma_5|_multiple_types|not_provided": 3,
    "Hearing_loss|_autosomal_recessive|Retinitis_pigmentosa-deafness_syndrome|not_provided": 1,
    "Hearing_impairment|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Cone-rod_dystrophy|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1|not_specified": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Pituitary_adenoma_5|_multiple_types|not_provided|Retinal_dystrophy": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified|Usher_syndrome_type_1": 1,
    "not_provided|not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 2,
    "not_provided|Stickler_syndrome|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|CDH23-related_disorder|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Pituitary_adenoma_5|_multiple_types|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinal_dystrophy|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|CDH23-related_disorder|Retinal_dystrophy|not_provided|Usher_syndrome_type_1|Hearing_loss|_autosomal_recessive": 1,
    "Retinal_dystrophy|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Syndromic_retinitis_pigmentosa|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_recessive|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|not_specified|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1D|CDH23-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Hearing_loss|_autosomal_recessive|not_specified|Deafness": 1,
    "not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1D|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "CDH23-related_disorder|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|CDH23-related_disorder|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|CDH23-related_disorder": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|CDH23-related_disorder": 1,
    "not_specified|not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_2A|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Rare_genetic_deafness|Usher_syndrome|Retinal_dystrophy|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "Usher_syndrome_type_1D|not_provided|Pituitary_adenoma_5|_multiple_types|Usher_syndrome|Inborn_genetic_diseases|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_specified": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|Usher_syndrome_type_1D": 1,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "not_provided|CDH23-related_disorder|not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome": 1,
    "Usher_syndrome_type_1D|not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Nonsyndromic_genetic_hearing_loss|not_specified|not_provided": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Rare_genetic_deafness": 1,
    "Hearing_impairment|Usher_syndrome_type_1|CDH23-related_disorder|not_provided": 1,
    "Usher_syndrome_type_1D|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified": 1,
    "not_provided|Usher_syndrome_type_1D|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|not_provided|Usher_syndrome_type_1D": 2,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|CDH23-related_disorder": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Pituitary_adenoma_5|_multiple_types|Usher_syndrome": 1,
    "not_provided|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 3,
    "Usher_syndrome|Pituitary_adenoma_5|_multiple_types|Rare_genetic_deafness|Retinal_dystrophy|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided|Rare_genetic_deafness": 1,
    "not_provided|CDH23-related_disorder|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 3,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "CDH23-related_disorder|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1|Hearing_impairment": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1": 1,
    "Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1|not_specified": 1,
    "not_specified|not_provided|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1|Optic_atrophy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|not_provided|Usher_syndrome_type_1D|Usher_syndrome_type_1": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_1D": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Pituitary_adenoma_5|_multiple_types": 1,
    "Rare_genetic_deafness|Pituitary_adenoma_5|_multiple_types|Neurodevelopmental_abnormality|Retinitis_pigmentosa-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|Retinal_dystrophy|not_specified": 1,
    "Retinal_dystrophy|Usher_syndrome_type_1": 2,
    "Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_specified": 1,
    "not_provided|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinal_dystrophy": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "CDH23-related_disorder|not_provided|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1D|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_2|not_specified": 1,
    "not_specified|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Usher_syndrome|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1D|Usher_syndrome_type_1|Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Usher_syndrome_type_1D": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases|not_specified": 2,
    "Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_impairment|Intellectual_disability": 1,
    "Usher_syndrome_type_1|Retinal_dystrophy|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Retinal_dystrophy|Usher_syndrome_type_1": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1|Hearing_impairment": 1,
    "not_provided|CDH23-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|CDH23-related_disorder": 1,
    "not_provided|Usher_syndrome_type_1D|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Usher_syndrome_type_1D|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided": 2,
    "Usher_syndrome_type_1D|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1": 1,
    "Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|Usher_syndrome_type_1D": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Retinal_dystrophy": 1,
    "not_specified|not_provided|Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified|not_provided": 1,
    "Retinal_dystrophy|Usher_syndrome_type_1D|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|not_provided|Usher_syndrome_type_1": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1D|CDH23-related_disorder|Galactosylceramide_beta-galactosidase_deficiency|Retinitis_pigmentosa-deafness_syndrome|Atypical_Gaucher_Disease|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_provided|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|Galactosylceramide_beta-galactosidase_deficiency|not_provided|Retinitis_pigmentosa-deafness_syndrome|Atypical_Gaucher_Disease|Combined_PSAP_deficiency|Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_loss|_autosomal_recessive|not_specified|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "CDH23-related_disorder|Usher_syndrome_type_1|not_provided": 1,
    "Metachromatic_leukodystrophy|Galactosylceramide_beta-galactosidase_deficiency|Usher_syndrome_type_1|not_specified|Retinitis_pigmentosa-deafness_syndrome|not_provided|Atypical_Gaucher_Disease|Combined_PSAP_deficiency|Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1D": 1,
    "not_specified|Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|CDH23-related_disorder": 1,
    "Pituitary_adenoma_5|_multiple_types|not_specified": 1,
    "Usher_syndrome_type_1D|CDH23-related_disorder|not_provided|Usher_syndrome_type_1|not_specified|Atypical_Gaucher_Disease|Combined_PSAP_deficiency|Autosomal_recessive_nonsyndromic_hearing_loss_12|Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy": 1,
    "not_provided|Usher_syndrome_type_1|Combined_PSAP_deficiency|not_specified|Atypical_Gaucher_Disease|Autosomal_recessive_nonsyndromic_hearing_loss_12|Metachromatic_leukodystrophy|Usher_syndrome_type_1D|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Combined_PSAP_deficiency|Usher_syndrome_type_1|Atypical_Gaucher_Disease|not_provided|Galactosylceramide_beta-galactosidase_deficiency|Usher_syndrome_type_1D|Metachromatic_leukodystrophy|not_specified": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "Pituitary_adenoma_5|_multiple_types|not_provided|Rare_genetic_deafness": 1,
    "Usher_syndrome_type_1D|Pituitary_adenoma_5|_multiple_types|Autosomal_recessive_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome|not_provided|not_specified|Usher_syndrome_type_1|USHER_SYNDROME|_TYPE_ID/F|_DIGENIC": 1,
    "not_specified|Pituitary_adenoma_5|_multiple_types|Usher_syndrome|Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "CDH23-related_disorder|not_provided|Hearing_impairment|Pituitary_adenoma_5|_multiple_types|not_specified|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome": 1,
    "CDH23-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Usher_syndrome_type_1|Pituitary_adenoma_5|_multiple_types": 1,
    "Rare_genetic_deafness|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1|not_provided": 1,
    "CDH23-related_disorder|Combined_PSAP_deficiency|Atypical_Gaucher_Disease|Usher_syndrome_type_1|Hearing_loss|_autosomal_recessive|not_provided|Galactosylceramide_beta-galactosidase_deficiency|Retinitis_pigmentosa-deafness_syndrome|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Metachromatic_leukodystrophy|not_specified": 1,
    "not_specified|CDH23-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Retinal_dystrophy|Usher_syndrome_type_1|Usher_syndrome_type_1D": 1,
    "Childhood_onset_hearing_loss|Pituitary_adenoma_5|_multiple_types|not_specified|Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Combined_PSAP_deficiency|Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinitis_pigmentosa-deafness_syndrome|CDH23-related_disorder|Atypical_Gaucher_Disease": 1,
    "Atypical_Gaucher_Disease|not_specified|not_provided|Usher_syndrome_type_1|Combined_PSAP_deficiency|Galactosylceramide_beta-galactosidase_deficiency|Usher_syndrome_type_1D|Metachromatic_leukodystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "Combined_PSAP_deficiency|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Retinitis_pigmentosa-deafness_syndrome|Atypical_Gaucher_Disease|Galactosylceramide_beta-galactosidase_deficiency|Hearing_loss|_autosomal_recessive|not_provided|Usher_syndrome_type_1D|Metachromatic_leukodystrophy": 1,
    "Combined_PSAP_deficiency|Inborn_genetic_diseases|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D|Retinitis_pigmentosa-deafness_syndrome|Atypical_Gaucher_Disease|Galactosylceramide_beta-galactosidase_deficiency|Hearing_loss|_autosomal_recessive|not_provided|Usher_syndrome_type_1|Metachromatic_leukodystrophy": 1,
    "Atypical_Gaucher_Disease|not_specified|not_provided|Usher_syndrome_type_1|Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Metachromatic_leukodystrophy": 1,
    "CDH23-related_disorder|Atypical_Gaucher_Disease|not_specified|not_provided|Usher_syndrome_type_1|Combined_PSAP_deficiency|Galactosylceramide_beta-galactosidase_deficiency|Usher_syndrome_type_1D|Metachromatic_leukodystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_12": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Usher_syndrome_type_1D|Usher_syndrome_type_1|not_specified": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinal_dystrophy|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|Hearing_impairment": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|CDH23-related_disorder|Atypical_Gaucher_Disease|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Metachromatic_leukodystrophy|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|not_specified|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|not_provided|VATER_association": 1,
    "Usher_syndrome_type_1D|not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Galactosylceramide_beta-galactosidase_deficiency|not_provided|Atypical_Gaucher_Disease|Combined_PSAP_deficiency|Metachromatic_leukodystrophy": 1,
    "not_specified|Usher_syndrome_type_1|Optic_atrophy|not_provided": 1,
    "not_provided|not_specified|Metachromatic_leukodystrophy|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|Atypical_Gaucher_Disease": 1,
    "CDH23-related_disorder|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|Pituitary_adenoma_5|_multiple_types|Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|CDH23-related_disorder|Combined_PSAP_deficiency|Atypical_Gaucher_Disease|Hearing_loss|_autosomal_recessive|not_provided|Usher_syndrome_type_1|Galactosylceramide_beta-galactosidase_deficiency|Retinitis_pigmentosa-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12|Metachromatic_leukodystrophy|Usher_syndrome_type_1D": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|CDH23-related_disorder|not_provided|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|Usher_syndrome_type_1D|not_provided": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1D|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|CDH23-related_disorder|PSAP-related_disorder|Atypical_Gaucher_Disease|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy|Usher_syndrome_type_1D": 1,
    "Metachromatic_leukodystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Galactosylceramide_beta-galactosidase_deficiency|Atypical_Gaucher_Disease|Combined_PSAP_deficiency": 2,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Atypical_Gaucher_Disease|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|Usher_syndrome_type_1D|Metachromatic_leukodystrophy": 1,
    "Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive|CDH23-related_disorder": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|CDH23-related_disorder|Atypical_Gaucher_Disease|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Atypical_Gaucher_Disease|Retinitis_pigmentosa-deafness_syndrome|not_provided|Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy": 3,
    "CDH23-related_disorder|PSAP-related_disorder|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Retinitis_pigmentosa-deafness_syndrome": 1,
    "PSAP-related_disorder|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Autosomal_recessive_nonsyndromic_hearing_loss_12|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1D|Retinitis_pigmentosa-deafness_syndrome": 1,
    "Metachromatic_leukodystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|Atypical_Gaucher_Disease": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Atypical_Gaucher_Disease|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|not_provided|Metachromatic_leukodystrophy": 1,
    "Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D|Atypical_Gaucher_Disease|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy": 1,
    "CDH23-related_disorder|Retinitis_pigmentosa-deafness_syndrome|Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Metachromatic_leukodystrophy|Atypical_Gaucher_Disease": 1,
    "Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency": 6,
    "Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency": 3,
    "Gaucher_disease_due_to_saposin_C_deficiency|Retinitis_pigmentosa-deafness_syndrome|not_provided|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Hearing_loss|_autosomal_recessive|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 4,
    "Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 4,
    "Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|not_provided": 2,
    "Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency": 1,
    "Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 6,
    "Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Autosomal_recessive_nonsyndromic_hearing_loss_12|Usher_syndrome_type_1D": 1,
    "Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|not_provided": 1,
    "Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency": 6,
    "Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency": 2,
    "Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency": 572,
    "Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency": 15,
    "not_provided|Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency": 1,
    "not_specified|not_provided|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "not_provided|Sphingolipid_activator_protein_1_deficiency": 7,
    "Sphingolipid_activator_protein_1_deficiency|Inborn_genetic_diseases|Metachromatic_leukodystrophy": 2,
    "Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Inborn_genetic_diseases|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Gaucher_disease_due_to_saposin_C_deficiency|not_provided|Galactosylceramide_beta-galactosidase_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy": 22,
    "not_provided|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "PSAP-related_disorder": 3,
    "not_provided|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency": 1,
    "Parkinson_disease_24|_autosomal_dominant|_susceptibility_to": 5,
    "Sphingolipid_activator_protein_1_deficiency|not_provided|Metachromatic_leukodystrophy": 2,
    "Sphingolipid_activator_protein_1_deficiency|Inborn_genetic_diseases": 16,
    "not_specified|not_provided|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy|not_provided": 3,
    "Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|not_provided": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 6,
    "Metachromatic_leukodystrophy|CDH23-related_disorder|Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|not_specified|Atypical_Gaucher_Disease|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Hearing_loss|_autosomal_recessive|not_specified|Atypical_Gaucher_Disease|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Metachromatic_leukodystrophy|Retinitis_pigmentosa-deafness_syndrome|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|not_specified|not_provided": 1,
    "Combined_PSAP_deficiency": 5,
    "not_provided|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy": 3,
    "Gaucher_disease_due_to_saposin_C_deficiency": 3,
    "not_provided|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Metachromatic_leukodystrophy|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|not_specified": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Inborn_genetic_diseases": 1,
    "Metachromatic_leukodystrophy|Combined_PSAP_deficiency|Galactosylceramide_beta-galactosidase_deficiency|Atypical_Gaucher_Disease": 1,
    "Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency": 16,
    "not_provided|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency|PSAP-related_disorder": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Metachromatic_leukodystrophy": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|not_provided|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy|Inborn_genetic_diseases": 1,
    "Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "not_provided|Sphingolipid_activator_protein_1_deficiency|Inborn_genetic_diseases|Metachromatic_leukodystrophy": 1,
    "Sphingolipid_activator_protein_1_deficiency|not_provided": 4,
    "not_provided|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|Metachromatic_leukodystrophy|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Atypical_Gaucher_Disease": 1,
    "PSAP-related_disorder|Sphingolipid_activator_protein_1_deficiency": 3,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|not_provided": 1,
    "Metachromatic_leukodystrophy|Gaucher_disease_due_to_saposin_C_deficiency": 1,
    "Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|not_specified|Krabbe_disease_due_to_saposin_A_deficiency|not_provided": 1,
    "Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to": 1,
    "PSAP-related_disorder|Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency": 2,
    "PSAP-related_disorder|Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency": 1,
    "Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency": 2,
    "not_provided|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|not_specified": 1,
    "Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|not_provided": 1,
    "Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency|not_provided": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|not_provided|Sphingolipid_activator_protein_1_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|PSAP-related_disorder|Inborn_genetic_diseases": 1,
    "Sphingolipid_activator_protein_1_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Inborn_genetic_diseases": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Metachromatic_leukodystrophy|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|PSAP-related_disorder": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Inborn_genetic_diseases|not_provided": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency|PSAP-related_disorder": 1,
    "Metachromatic_leukodystrophy|Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency": 1,
    "not_specified|Sphingolipid_activator_protein_1_deficiency": 1,
    "PSAP-related_disorder|Metachromatic_leukodystrophy|not_provided|Sphingolipid_activator_protein_1_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy": 1,
    "Sphingolipid_activator_protein_1_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|not_specified": 1,
    "Metachromatic_leukodystrophy|Inborn_genetic_diseases": 6,
    "Parkinson_disease|_late-onset|Sphingolipid_activator_protein_1_deficiency|not_specified": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|PSAP-related_disorder|Metachromatic_leukodystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Metachromatic_leukodystrophy|Inborn_genetic_diseases": 1,
    "Combined_PSAP_deficiency|Metachromatic_leukodystrophy": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|PSAP-related_disorder|Inborn_genetic_diseases": 1,
    "Sphingolipid_activator_protein_1_deficiency|PSAP-related_disorder": 3,
    "Inborn_genetic_diseases|Sphingolipid_activator_protein_1_deficiency|not_provided|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|not_specified": 1,
    "PSAP-related_disorder|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy|not_provided": 1,
    "not_provided|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Inborn_genetic_diseases|Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy|Atypical_Gaucher_Disease": 1,
    "Sphingolipid_activator_protein_1_deficiency|Neuromuscular_disease": 1,
    "Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to": 1,
    "not_provided|Inborn_genetic_diseases|Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency": 1,
    "not_provided|Metachromatic_leukodystrophy|PSAP-related_disorder|Sphingolipid_activator_protein_1_deficiency": 1,
    "not_provided|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency": 2,
    "Inborn_genetic_diseases|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Metachromatic_leukodystrophy|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|not_provided": 1,
    "Metachromatic_leukodystrophy|Krabbe_disease_due_to_saposin_A_deficiency|Sphingolipid_activator_protein_1_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency": 1,
    "PSAP-related_disorder|Metachromatic_leukodystrophy|Sphingolipid_activator_protein_1_deficiency|not_provided": 1,
    "not_provided|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Inborn_genetic_diseases": 1,
    "Metachromatic_leukodystrophy|PSAP-related_disorder|Sphingolipid_activator_protein_1_deficiency|not_provided": 1,
    "not_provided|Sphingolipid_activator_protein_1_deficiency|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to": 1,
    "Sphingolipid_activator_protein_1_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency": 1,
    "Sphingolipid_activator_protein_1_deficiency|Metachromatic_leukodystrophy|Parkinson_disease_24|_autosomal_dominant|_susceptibility_to": 1,
    "Metachromatic_leukodystrophy|not_specified|not_provided|Krabbe_disease_due_to_saposin_A_deficiency|Combined_PSAP_deficiency|Gaucher_disease_due_to_saposin_C_deficiency|Sphingolipid_activator_protein_1_deficiency": 1,
    "not_provided|not_specified|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "not_specified|Gaucher_disease_due_to_saposin_C_deficiency|Combined_PSAP_deficiency|Sphingolipid_activator_protein_1_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Atypical_Gaucher_Disease|not_provided|Combined_PSAP_deficiency|Metachromatic_leukodystrophy|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Atypical_Gaucher_Disease|Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|Metachromatic_leukodystrophy": 4,
    "Atypical_Gaucher_Disease|Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|not_provided|Metachromatic_leukodystrophy": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|Combined_PSAP_deficiency|Atypical_Gaucher_Disease|Metachromatic_leukodystrophy|not_provided": 1,
    "not_provided|Sphingolipid_activator_protein_1_deficiency|Combined_PSAP_deficiency|Krabbe_disease_due_to_saposin_A_deficiency": 1,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 305,
    "not_provided|Skeletal_dysplasia|Larsen_syndrome|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 25,
    "Larsen_syndrome|Skeletal_dysplasia|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 33,
    "Skeletal_dysplasia|Larsen_syndrome|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 57,
    "Inborn_genetic_diseases|Larsen_syndrome|Skeletal_dysplasia|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 2,
    "not_provided|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 9,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|not_provided|Larsen-like_syndrome|_B3GAT3_type": 1,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 11,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Skeletal_dysplasia|Inborn_genetic_diseases|Larsen_syndrome|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|not_provided": 6,
    "Inborn_genetic_diseases|Skeletal_dysplasia|Larsen_syndrome|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 1,
    "not_specified|Skeletal_dysplasia|Larsen_syndrome|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 2,
    "CHST3-related_disorder|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 2,
    "not_specified|not_provided|Larsen_syndrome|Skeletal_dysplasia|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 1,
    "CHST3-related_disorder": 1,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Larsen_syndrome|Skeletal_dysplasia|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 1,
    "not_specified|not_provided|Skeletal_dysplasia|Larsen_syndrome|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Larsen-like_syndrome|_B3GAT3_type|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 1,
    "not_specified|not_provided|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 1,
    "not_provided|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|not_specified|Larsen-like_syndrome|_B3GAT3_type": 1,
    "not_provided|Larsen_syndrome|Skeletal_dysplasia|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 17,
    "not_specified|Larsen_syndrome|Skeletal_dysplasia|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Skeletal_dysplasia|Larsen_syndrome|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia_with_congenital_joint_dislocations": 1,
    "ASCC1-related_disorder": 3,
    "ASCC1-related_disorder|not_provided": 3,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_2": 8,
    "not_provided|Spinal_muscular_atrophy_with_congenital_bone_fractures_2": 3,
    "BARRETT_ESOPHAGUS/ESOPHAGEAL_ADENOCARCINOMA|Spinal_muscular_atrophy_with_congenital_bone_fractures_2|not_provided|not_specified": 1,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Barrett_esophagus": 1,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_2|not_provided": 2,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Spinal_muscular_atrophy_with_congenital_bone_fractures_2|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|Spinal_muscular_atrophy_with_congenital_bone_fractures_2|Centronuclear_myopathy": 1,
    "Inborn_genetic_diseases|Spinal_muscular_atrophy_with_congenital_bone_fractures_2": 1,
    "not_provided|ASCC1-related_disorder": 3,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_2|See_cases|ASCC1-related_disorder|not_provided": 1,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_2|ASCC1-related_disorder|not_provided": 1,
    "not_provided|Proximal_myopathy_with_extrapyramidal_signs": 3,
    "Proximal_myopathy_with_extrapyramidal_signs": 7,
    "Proximal_myopathy_with_extrapyramidal_signs|not_provided": 5,
    "not_provided|MICU1-related_disorder": 2,
    "MICU1-related_disorder|not_provided|Proximal_myopathy_with_extrapyramidal_signs": 1,
    "Proximal_myopathy_with_extrapyramidal_signs|not_provided|Abnormality_of_the_nervous_system": 1,
    "MICU1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Proximal_myopathy_with_extrapyramidal_signs": 1,
    "Proximal_myopathy_with_extrapyramidal_signs|not_provided|Neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "P4HA1-related_disorder": 11,
    "Congenital_disorder_of_connective_tissue": 1,
    "not_specified|P4HA1-related_disorder": 1,
    "Joubert_syndrome_36|not_specified": 1,
    "not_specified|FAM149B1-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_36": 1,
    "FAM149B1-related_disorder": 2,
    "MRPS16-related_disorder|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_2|not_provided": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_2|not_provided": 1,
    "MRPS16-related_disorder": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_2": 1,
    "not_provided|MRPS16-related_disorder": 1,
    "CFAP70-related_condition": 1,
    "Spermatogenic_failure_41": 1,
    "not_specified|USP54-related_disorder": 1,
    "USP54-related_disorder": 2,
    "USP54-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_59": 15,
    "not_specified|Intellectual_developmental_disorder_59": 1,
    "CAMK2G-related_syndromic_intellectual_disability": 1,
    "CAMK2G-related_disorder": 8,
    "not_specified|CAMK2G-related_disorder": 1,
    "CAMK2G-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_59|Intellectual_disability|_severe|Generalized_hypotonia|Global_developmental_delay|Autism": 1,
    "Intellectual_developmental_disorder_59|not_provided": 3,
    "Quebec_platelet_disorder": 45,
    "not_provided|Quebec_platelet_disorder": 10,
    "Quebec_platelet_disorder|not_provided": 2,
    "not_specified|Quebec_platelet_disorder|Alzheimer_disease_type_1": 1,
    "C10orf55-related_disorder": 2,
    "PLAU-related_disorder": 2,
    "not_specified|Quebec_platelet_disorder": 4,
    "PLAU-related_disorder|Quebec_platelet_disorder|not_provided": 1,
    "PLAU-related_disorder|Quebec_platelet_disorder": 1,
    "not_provided|Quebec_platelet_disorder|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Quebec_platelet_disorder": 1,
    "not_provided|Alzheimer_disease|_late-onset|_susceptibility_to": 1,
    "Quebec_platelet_disorder|not_specified": 3,
    "Quebec_platelet_disorder|Alzheimer_disease_type_1": 1,
    "not_specified|PLAU-related_disorder": 1,
    "not_provided|PLAU-related_disorder|not_specified|Quebec_platelet_disorder": 1,
    "Dilated_cardiomyopathy_1W": 653,
    "not_provided|Dilated_cardiomyopathy_1W": 24,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 97,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15|not_provided": 2,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 94,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 7,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W": 15,
    "not_provided|not_specified|Dilated_cardiomyopathy_1W|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1W": 3,
    "not_specified|Dilated_cardiomyopathy_1W": 9,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15": 4,
    "Primary_familial_dilated_cardiomyopathy|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "not_provided|Dilated_cardiomyopathy_1W|not_specified": 2,
    "not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W|not_specified": 3,
    "Dilated_cardiomyopathy_1W|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_provided": 3,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_provided": 5,
    "Dilated_cardiomyopathy_1W|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified": 1,
    "Dilated_cardiomyopathy_1W|VCL-related_disorder": 1,
    "Dilated_cardiomyopathy_1W|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1W": 7,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1W|not_specified": 13,
    "Cardiomyopathy|VCL-related_disorder|Dilated_cardiomyopathy_1W|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|not_provided": 9,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 22,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 9,
    "VCL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1W": 1,
    "Dilated_cardiomyopathy_1W|not_specified|Hypertrophic_cardiomyopathy_15": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype": 4,
    "not_provided|Dilated_cardiomyopathy_1W|not_specified|Cardiovascular_phenotype": 2,
    "not_provided|VCL-related_disorder|Dilated_cardiomyopathy_1W": 1,
    "Wolff-Parkinson-White_pattern|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "VCL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_provided": 9,
    "Dilated_cardiomyopathy_1W|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_provided|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_15": 5,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1W|not_provided": 19,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 9,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1W|not_provided|Hypertrophic_cardiomyopathy_15": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|VCL-related_disorder|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 6,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_provided|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15": 1,
    "Dilated_cardiomyopathy_1W|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "Dilated_cardiomyopathy_1W|not_specified|not_provided": 6,
    "not_specified|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|not_provided": 1,
    "VCL-related_disorder": 2,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_specified": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1W|not_provided|Cardiovascular_phenotype": 7,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W|not_specified|Hypertrophic_cardiomyopathy_15": 1,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|VCL-related_disorder|Dilated_cardiomyopathy_1W|Primary_dilated_cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1W|VCL-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1W": 3,
    "Short_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 3,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1W|not_specified|not_provided|VCL-related_disorder": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_specified|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1W": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_provided|Hypertrophic_cardiomyopathy_15": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|not_provided": 2,
    "not_specified|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "Dilated_cardiomyopathy_1W|not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_15": 1,
    "not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_provided": 1,
    "Dilated_cardiomyopathy_1W|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1W": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W": 1,
    "not_provided|not_specified|Congestive_heart_failure|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1W|Ventricular_tachycardia": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|not_provided|VCL-related_disorder": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1W|Sudden_unexplained_death": 1,
    "not_provided|not_specified|VCL-related_disorder|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Aborted_sudden_cardiac_death": 1,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|VCL-related_disorder|not_specified": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1W": 1,
    "Dilated_cardiomyopathy_1W|not_provided|Hypertrophic_cardiomyopathy_15": 2,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|VCL-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|not_specified": 3,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "not_specified|Dilated_cardiomyopathy_1W|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|VCL-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_1W|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern": 1,
    "Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1W|Primary_dilated_cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|VCL-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|VCL-related_disorder|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1W": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1W": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1W": 2,
    "Cardiovascular_phenotype|VCL-related_disorder": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Aganglionic_megacolon|not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|Dilated_cardiomyopathy_1S|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1W": 1,
    "VCL-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "not_specified|Dilated_cardiomyopathy_1W|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "VCL-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "Dilated_cardiomyopathy_1W|VCL-related_disorder|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1W|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15": 1,
    "VCL-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1W|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified|not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_with_left_ventricular_noncompaction": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|not_specified": 1,
    "Dilated_cardiomyopathy_1W|not_provided|VCL-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15": 1,
    "not_provided|Hypertrophic_cardiomyopathy_15": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1W|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|VCL-related_disorder|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1W": 1,
    "Dilated_cardiomyopathy_1W|not_specified|Cardiovascular_phenotype|VCL-related_disorder": 1,
    "not_specified|Dilated_cardiomyopathy_1W|Hypertrophic_cardiomyopathy_15|VCL-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_15|Dilated_cardiomyopathy_1W|Dilated_Cardiomyopathy|_Dominant": 1,
    "Adenosine_kinase_deficiency": 34,
    "Adenosine_kinase_deficiency|not_provided": 11,
    "not_provided|Adenosine_kinase_deficiency": 5,
    "ADK-related_disorder|not_provided": 2,
    "ADK-related_disorder": 1,
    "not_provided|ADK-related_disorder": 2,
    "KAT6B-Related_Spectrum_Disorders": 5,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 36,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 136,
    "Genitopatellar_syndrome": 735,
    "Genitopatellar_syndrome|Inborn_genetic_diseases": 21,
    "not_provided|Genitopatellar_syndrome": 35,
    "Inborn_genetic_diseases|Genitopatellar_syndrome": 29,
    "KAT6B-related_disorder": 24,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome|not_provided": 5,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome": 12,
    "Genitopatellar_syndrome|not_provided": 34,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome|Inborn_genetic_diseases": 1,
    "KAT6B-Related_Spectrum_Disorders|not_provided|Inborn_genetic_diseases|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "not_specified|Genitopatellar_syndrome": 9,
    "Genitopatellar_syndrome|not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 3,
    "not_provided|Genitopatellar_syndrome|KAT6B-related_disorder|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "KAT6B-related_disorder|Genitopatellar_syndrome": 4,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|not_provided|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "not_specified|not_provided|Genitopatellar_syndrome": 5,
    "Genitopatellar_syndrome|KAT6B-related_disorder": 13,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome|not_specified": 2,
    "Genitopatellar_syndrome|not_specified": 7,
    "Inborn_genetic_diseases|Genitopatellar_syndrome|not_provided": 3,
    "Genitopatellar_syndrome|Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 3,
    "not_provided|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 10,
    "Genitopatellar_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome": 3,
    "KAT6B-related_disorder|Inborn_genetic_diseases|Genitopatellar_syndrome|not_provided": 1,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_specified": 2,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided|not_specified": 3,
    "Genitopatellar_syndrome|not_provided|KAT6B-related_disorder": 3,
    "Inborn_genetic_diseases|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 11,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided": 11,
    "Genitopatellar_syndrome|Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided": 1,
    "Genitopatellar_syndrome|not_specified|Inborn_genetic_diseases": 3,
    "Genitopatellar_syndrome|not_provided|not_specified": 2,
    "KAT6B-related_disorder|not_provided|Genitopatellar_syndrome": 5,
    "Genitopatellar_syndrome|KAT6B-related_disorder|not_provided": 3,
    "Genitopatellar_syndrome|Obesity": 1,
    "KAT6B-related_disorder|Genitopatellar_syndrome|not_provided": 1,
    "Hypospadias|Inborn_genetic_diseases": 1,
    "Intellectual_disability|not_provided|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "Genitopatellar_syndrome|not_specified|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 2,
    "not_specified|Genitopatellar_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|KAT6B-related_disorder": 1,
    "not_provided|Autosomal_dominant_KAT6B-related_disorders|not_specified|Genitopatellar_syndrome": 1,
    "Inborn_genetic_diseases|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided": 1,
    "Macrocephaly|Generalized_joint_hypermobility|Joint_laxity|Delayed_speech_and_language_development|Seizure|not_provided|Genitopatellar_syndrome|Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "Genitopatellar_syndrome|Nephronophthisis": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided": 6,
    "Inborn_genetic_diseases|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_specified": 1,
    "KAT6B-related_disorder|Genitopatellar_syndrome|not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "not_provided|Genitopatellar_syndrome|not_specified": 3,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome|KAT6B-related_disorder": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Genitopatellar_syndrome": 1,
    "not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 7,
    "Genitopatellar_syndrome|Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_specified": 1,
    "not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Intellectual_disability": 1,
    "Arachnodactyly|TWIST1-related_craniosynostosis": 1,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided|KAT6B-related_disorder": 1,
    "not_specified|not_provided|Genitopatellar_syndrome|Intellectual_disability": 1,
    "not_provided|Genitopatellar_syndrome|KAT6B-related_disorder": 1,
    "not_provided|KAT6B-related_disorder|Genitopatellar_syndrome": 2,
    "not_specified|Genitopatellar_syndrome|not_provided": 1,
    "Genitopatellar_syndrome|not_specified|not_provided": 1,
    "Genitopatellar_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome|not_provided|KAT6B-related_disorder": 1,
    "KAT6B-related_disorder|not_provided|Genitopatellar_syndrome|not_specified|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Neurodevelopmental_disorder|not_provided": 1,
    "Blepharophimosis|Telecanthus|Vesicoureteral_reflux|Abnormal_facial_shape|Bulbous_nose|Renal_hypoplasia|Epicanthus|Intellectual_disability|Hypoplasia_of_the_maxilla|Poor_speech": 1,
    "not_provided|Genitopatellar_syndrome|Inborn_genetic_diseases": 3,
    "KAT6B-related_disorder|KAT6B-realted_disoder|Genitopatellar_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Genitopatellar_syndrome": 1,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_specified|not_provided": 3,
    "not_provided|Genitopatellar_syndrome|KAT6B-related_disorder|not_specified": 1,
    "KAT6B-related_disorder|not_provided|Inborn_genetic_diseases|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "Inborn_genetic_diseases|KAT6B-related_disorder|Genitopatellar_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Genitopatellar_syndrome": 2,
    "not_provided|Genitopatellar_syndrome|KAT6B-related_disorder|Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "not_specified|not_provided|KAT6B-related_disorder|Inborn_genetic_diseases|Genitopatellar_syndrome": 1,
    "Autosomal_dominant_KAT6B-related_disorders": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Inborn_genetic_diseases|not_provided": 1,
    "Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|KAT6B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Genitopatellar_syndrome": 1,
    "Genitopatellar_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|Genitopatellar_syndrome": 1,
    "not_specified|Genitopatellar_syndrome|KAT6B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KAT6B-related_disorder|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided": 1,
    "Intellectual_disability|Genitopatellar_syndrome": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 4,
    "Developmental_disorder|not_provided|KAT6B-related_multiple_congenital_anomalies_syndrome": 1,
    "Genitopatellar_syndrome|not_provided|KAT6B-related_disorder|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "Cryptorchidism|Hypertelorism|Short_distal_phalanx_of_toe|Tapered_finger|Neuropathic_spinal_arthropathy|Clubfoot|Intellectual_disability|Abnormal_facial_shape|Short_nose|not_provided": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_provided|Genitopatellar_syndrome": 1,
    "Inborn_genetic_diseases|Genitopatellar_syndrome|Left_ventricular_noncompaction": 1,
    "Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "Genitopatellar_syndrome|not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|not_specified": 1,
    "not_provided|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|KAT6B-related_multiple_congenital_anomalies_syndrome": 1,
    "KAT6B-related_disorder|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "not_provided|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type|KAT6B-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Genitopatellar_syndrome": 1,
    "KAT6B-related_disorder|not_provided": 1,
    "KAT6B-related_disorder|Genitopatellar_syndrome|Inborn_genetic_diseases": 1,
    "KAT6B-related_disorder|not_provided|Genitopatellar_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_SBBYS_type": 1,
    "not_provided|KAT6B-Related_Spectrum_Disorders": 1,
    "Oculocutaneous_albinism_type_7": 2,
    "LRMDA-related_disorder": 1,
    "Oculocutaneous_albinism_type_7|not_provided|LRMDA-related_disorder": 1,
    "not_specified|not_provided|Oculocutaneous_albinism_type_7": 1,
    "Oculocutaneous_albinism_type_7|not_specified|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_7": 2,
    "not_provided|LRMDA-related_disorder": 1,
    "LRMDA-related_disorder|not_provided": 1,
    "Oculocutaneous_albinism_type_7|not_provided": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 830,
    "not_provided|KCNMA1-related_disorder": 4,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided": 60,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 75,
    "Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided": 5,
    "KCNMA1-related_disorder|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 6,
    "not_provided|See_cases|Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 2,
    "not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 6,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Inborn_genetic_diseases": 12,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|KCNMA1-related_disorder": 2,
    "Hypotonia|Global_developmental_delay|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 10,
    "KCNMA1-related_disorder|Inborn_genetic_diseases|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome|not_specified|not_provided": 1,
    "not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided": 2,
    "not_specified|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 10,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_specified": 6,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Liang-Wang_syndrome|not_provided": 1,
    "KCNMA1-related_disorder": 19,
    "Liang-Wang_syndrome": 13,
    "Intellectual_disability|not_provided|Liang-Wang_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|KCNMA1-related_disorder": 8,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Liang-Wang_syndrome|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|not_provided": 1,
    "KCNMA1-related_disorder|Liang-Wang_syndrome|not_provided|Intellectual_disability": 1,
    "Seizure|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided": 1,
    "not_specified|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|KCNMA1-related_disorder": 1,
    "not_specified|KCNMA1-related_disorder|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Liang-Wang_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome": 1,
    "not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome|KCNMA1-related_disorder": 1,
    "KCNMA1-related_disorder|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 7,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Liang-Wang_syndrome": 1,
    "not_provided|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Cerebellar_atrophy|_developmental_delay|_and_seizures|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Liang-Wang_syndrome": 1,
    "Cerebellar_atrophy|_developmental_delay|_and_seizures": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|not_provided|Inborn_genetic_diseases": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Cerebellar_atrophy|_developmental_delay|_and_seizures|not_provided": 1,
    "not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided|KCNMA1-related_disorder": 1,
    "Liang-Wang_syndrome|not_provided": 1,
    "not_provided|KCNMA1-related_disorder|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Liang-Wang_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Liang-Wang_syndrome|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|not_provided": 1,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|KCNMA1-related_disorder|not_specified": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_16": 4,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided|KCNMA1-related_disorder": 2,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided|Cerebellar_atrophy|_developmental_delay|_and_seizures|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Cerebellar_atrophy|_developmental_delay|_and_seizures|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "KCNMA1-related_disorder|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided": 3,
    "Liang-Wang_syndrome|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures": 1,
    "Liang-Wang_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Liang-Wang_syndrome|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 4,
    "not_specified|not_provided|Cerebellar_atrophy|_developmental_delay|_and_seizures|Liang-Wang_syndrome|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Inborn_genetic_diseases": 1,
    "not_specified|KCNMA1-related_disorder|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "KCNMA1-related_disorder|not_provided": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided|Cerebellar_atrophy|_developmental_delay|_and_seizures|KCNMA1-related_disorder|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|KCNMA1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Liang-Wang_syndrome|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|not_provided": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "KCNMA1-related_disorder|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|not_specified|not_provided": 1,
    "KCNMA1-related_disorder|not_provided|not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "KCNMA1-related_disorder|not_specified|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 2,
    "not_provided|not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Inborn_genetic_diseases|Cerebellar_atrophy|_developmental_delay|_and_seizures": 1,
    "not_provided|Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "KCNMA1-related_disorder|Infantile_epileptic_dyskinetic_encephalopathy|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_specified|not_provided": 2,
    "Cerebellar_atrophy|_developmental_delay|_and_seizures|not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "not_provided|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Liang-Wang_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Liang-Wang_syndrome": 1,
    "KCNMA1-related_disorder|not_provided|not_specified|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Intellectual_disability": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_16|Cerebellar_atrophy|_developmental_delay|_and_seizures|Liang-Wang_syndrome|not_specified": 1,
    "KCNMA1-related_disorder|Inborn_genetic_diseases|Generalized_epilepsy-paroxysmal_dyskinesia_syndrome": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy-paroxysmal_dyskinesia_syndrome|Cerebellar_atrophy|_developmental_delay|_and_seizures": 1,
    "DLG5-related_disorder|not_specified": 1,
    "DLG5-related_disorder": 7,
    "Yuksel-Vogel-Bauer_syndrome": 2,
    "not_specified|DLG5-related_disorder": 1,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 134,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 44,
    "POLR-related_leukodystrophy": 9,
    "not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 44,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukodystrophy": 1,
    "POLR3A-related_disorder": 12,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome": 5,
    "Leukodystrophy|Neonatal_pseudo-hydrocephalic_progeroid_syndrome": 2,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Leukodystrophy": 2,
    "Leukodystrophy|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 4,
    "POLR3A-related_neurological_disorders": 1,
    "not_provided|POLR3A-related_disorder": 4,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukodystrophy|POLR3A-related_disorder": 1,
    "Leukodystrophy|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 7,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|not_provided": 4,
    "not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|POLR3A-related_disorder": 2,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Hypomyelination-hypogonadotropic_hypogonadism-hypodontia_syndrome|not_provided": 1,
    "Leukodystrophy|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 2,
    "POLR3A-related_disorder|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 3,
    "Leukodystrophy|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_specified": 1,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 4,
    "not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|POLR-related_leukodystrophy": 2,
    "Leukodystrophy|not_provided": 7,
    "not_provided|POLR3A-related_disorder|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 3,
    "POLR3A-related_neurological_disorders|not_provided": 2,
    "POLR3A-related_disorder|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukodystrophy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 2,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Wiedemann-Rautenstrauch-like_progeroid_syndrome|not_provided": 1,
    "Wiedemann-Rautenstrauch-like_progeroid_syndrome|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukodystrophy|not_provided": 1,
    "not_provided|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "POLR3A-related_disorder|not_provided": 8,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 2,
    "not_provided|Leukodystrophy|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "not_provided|Leukodystrophy": 2,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Leukodystrophy|not_provided": 2,
    "POLR3A-related_disorder|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_specified|not_provided": 1,
    "Leukodystrophy|POLR3A-related_disorder": 1,
    "POLR3A-related_neurological_disorders|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 1,
    "POLR3A-related_disorder|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukodystrophy|not_provided": 1,
    "Leukodystrophy|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|not_provided": 1,
    "Leukodystrophy|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 3,
    "not_specified|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Inborn_genetic_diseases|Leukodystrophy": 1,
    "not_specified|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 3,
    "POLR3A-related_disorder|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 2,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided|Leukodystrophy": 2,
    "POLR-related_leukodystrophy|POLR3A-related_disorder|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 1,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|not_provided|Hereditary_ataxia": 1,
    "Movement_disorder|not_specified|not_provided|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|POLR3A-related_disorder|Hereditary_ataxia|POLR3A-related_neurological_disorders|POLR-related_leukodystrophy|Inborn_genetic_diseases|Spastic_ataxia": 1,
    "not_provided|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Hypomyelination-hypogonadotropic_hypogonadism-hypodontia_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "not_provided|POLR3A-related_disorder|Inborn_genetic_diseases": 1,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "POLR-related_leukodystrophy|POLR3A-related_disorder|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Intellectual_disability": 1,
    "Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_specified|not_provided": 1,
    "POLR3A-related_disorder|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 1,
    "Leukodystrophy|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_specified|not_provided": 1,
    "not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Neonatal_pseudo-hydrocephalic_progeroid_syndrome": 1,
    "Inborn_genetic_diseases|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 2,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|POLR3A-related_disorder|not_provided": 1,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Neonatal_pseudo-hydrocephalic_progeroid_syndrome": 1,
    "POLR3A-related_disorder|not_specified|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Neonatal_pseudo-hydrocephalic_progeroid_syndrome|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|POLR-related_leukodystrophy|Wiedemann-Rautenstrauch-like_progeroid_syndrome|not_provided": 1,
    "not_specified|POLR3A-related_disorder|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "Diamond-Blackfan_anemia|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "POLR-related_leukodystrophy|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_3": 38,
    "POLR-related_leukodystrophy|not_provided|Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_3|not_specified": 1,
    "not_specified|POLR-related_leukodystrophy|not_provided|Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia": 1,
    "RPS24-related_disorder|not_specified": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_3": 8,
    "Diamond-Blackfan_anemia_3|not_provided": 2,
    "not_provided|Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia": 3,
    "not_specified|Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia|not_provided": 1,
    "RPS24-related_disorder|Diamond-Blackfan_anemia|not_provided|Diamond-Blackfan_anemia_3": 1,
    "not_specified|Diamond-Blackfan_anemia|RPS24-related_disorder": 1,
    "RPS24-related_disorder|not_specified|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_3": 1,
    "RPS24-related_disorder": 10,
    "Diamond-Blackfan_anemia|RPS24-related_disorder|Diamond-Blackfan_anemia_3": 1,
    "not_specified|RPS24-related_disorder|Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia": 1,
    "RPS24-related_disorder|not_specified|not_provided|Diamond-Blackfan_anemia_3|Diamond-Blackfan_anemia": 1,
    "not_provided|not_specified|Diamond-Blackfan_anemia_3": 1,
    "Diamond-Blackfan_anemia_3|RPS24-related_disorder|not_provided": 1,
    "not_provided|Diamond-Blackfan_anemia_3": 4,
    "not_provided|RPS24-related_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 38,
    "not_provided|Neurodevelopmental_abnormality|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "Syndromic_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies|not_specified": 1,
    "ZMIZ1-related_disorder|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "See_cases|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 7,
    "not_specified|ZMIZ1-related_disorder": 1,
    "ZMIZ1-related_disorder": 10,
    "Inborn_genetic_diseases|ZMIZ1-related_disorder|not_provided": 1,
    "not_provided|ZMIZ1-related_disorder": 3,
    "ZMIZ1-related_disorder|Syndromic_neurodevelopmental_disorder": 1,
    "Syndromic_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 3,
    "not_provided|Syndromic_neurodevelopmental_disorder": 1,
    "Syndromic_neurodevelopmental_disorder|not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies|not_provided": 5,
    "ZMIZ1-related_disorder|not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "not_specified|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies|Inborn_genetic_diseases": 1,
    "Syndromic_neurodevelopmental_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_skeletal_anomalies|Syndromic_neurodevelopmental_disorder": 1,
    "SFTPA2-related_disorder": 20,
    "Mullegama-Klein-Martinez_syndrome": 25,
    "not_specified|not_provided|Interstitial_lung_disease_2": 2,
    "not_provided|Inborn_genetic_diseases|Interstitial_lung_disease_2": 1,
    "not_provided|Interstitial_lung_disease_2": 6,
    "SFTPA2-related_disorder|not_provided": 2,
    "SFTPA2-related_disorder|not_provided|Interstitial_lung_disease_2": 1,
    "not_specified|SFTPA2-related_disorder|not_provided": 1,
    "Interstitial_lung_disease_2|SFTPA2-related_disorder|not_specified|not_provided": 1,
    "not_provided|SFTPA2-related_disorder": 1,
    "not_specified|not_provided|SFTPA2-related_disorder": 1,
    "SFTPA2-related_disorder|not_provided|not_specified": 1,
    "Interstitial_lung_disease_2|SFTPA2-related_disorder|not_provided": 1,
    "SFTPA1-related_disorder": 15,
    "Interstitial_lung_disease_1": 7,
    "not_specified|SFTPA1-related_disorder|See_cases|not_provided": 1,
    "SFTPA1-related_disorder|not_provided": 1,
    "not_specified|SFTPA1-related_disorder|not_provided": 2,
    "not_provided|SFTPA1-related_disorder|not_specified": 1,
    "SFTPA1-related_disorder|not_specified|not_provided": 1,
    "Interstitial_lung_disease_1|not_specified|not_provided": 1,
    "Proximal_16p11.2_microdeletion_syndrome": 1,
    "Interstitial_lung_disease_1|not_specified": 1,
    "SFTPA1-related_disorder|not_provided|not_specified": 1,
    "not_specified|Interstitial_lung_disease_1": 1,
    "not_specified|Interstitial_lung_disease_1|SFTPA1-related_disorder": 1,
    "SFTPA1-related_disorder|Pulmonary_fibrosis|_idiopathic|_susceptibility_to|not_specified|not_provided": 1,
    "Respiratory_distress_associated_with_prematurity|Interstitial_lung_disease_1|not_specified": 1,
    "Oculopharyngeal_myopathy_with_leukoencephalopathy_1": 2,
    "SFTPD-related_disorder": 3,
    "SFTPD-related_disorder|not_specified|not_provided": 1,
    "ANXA11-related_disorder": 20,
    "Inclusion_body_myopathy_and_brain_white_matter_abnormalities": 3,
    "ANXA11-related_disorder|not_provided": 20,
    "ANXA11-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_23|not_provided": 2,
    "not_provided|ANXA11-related_disorder": 21,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_23|not_provided": 1,
    "not_provided|Inclusion_body_myopathy_and_brain_white_matter_abnormalities": 8,
    "Inclusion_body_myopathy_and_brain_white_matter_abnormalities|not_provided": 16,
    "Amyotrophic_lateral_sclerosis_type_23|ANXA11-related_disorder|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_23": 3,
    "ANXA11-related_disorder|Amyotrophic_lateral_sclerosis_type_23|not_provided": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_23|ANXA11-related_disorder": 2,
    "not_provided|ANXA11-related_disorder|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_23|Inclusion_body_myopathy_and_brain_white_matter_abnormalities|not_provided": 1,
    "not_provided|ANXA11-related_disorder|Amyotrophic_lateral_sclerosis_type_23": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_23": 1,
    "Inborn_genetic_diseases|ANXA11-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|ANXA11-related_disorder": 1,
    "Inborn_genetic_diseases|ANXA11-related_disorder|not_provided": 1,
    "ANXA11-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_23": 1,
    "Oculopharyngeal_muscular_dystrophy_1": 17,
    "Inclusion_body_myopathy_and_brain_white_matter_abnormalities|Amyotrophic_lateral_sclerosis_type_23|not_provided": 1,
    "not_provided|ANXA11-related_disorder|Amyotrophic_lateral_sclerosis_type_23|Amyotrophic_lateral_sclerosis": 1,
    "ANXA11-related_disorder|Inborn_genetic_diseases": 1,
    "Hepatic_methionine_adenosyltransferase_deficiency": 277,
    "Hepatic_methionine_adenosyltransferase_deficiency|not_provided": 18,
    "not_provided|Hepatic_methionine_adenosyltransferase_deficiency": 24,
    "Inborn_genetic_diseases|not_specified|Hepatic_methionine_adenosyltransferase_deficiency": 1,
    "MAT1A-related_disorder|Hepatic_methionine_adenosyltransferase_deficiency": 4,
    "not_provided|Hepatic_methionine_adenosyltransferase_deficiency|not_specified": 2,
    "not_specified|Hepatic_methionine_adenosyltransferase_deficiency|not_provided": 3,
    "not_specified|not_provided|Hepatic_methionine_adenosyltransferase_deficiency": 2,
    "Hepatic_methionine_adenosyltransferase_deficiency|not_specified": 4,
    "not_specified|Hepatic_methionine_adenosyltransferase_deficiency": 3,
    "Hepatic_methionine_adenosyltransferase_deficiency|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Hepatic_methionine_adenosyltransferase_deficiency": 6,
    "MAT1A-related_disorder|not_provided|Hepatic_methionine_adenosyltransferase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Hepatic_methionine_adenosyltransferase_deficiency": 1,
    "Hepatic_methionine_adenosyltransferase_deficiency|MAT1A-related_disorder|not_specified": 1,
    "not_provided|Hepatic_methionine_adenosyltransferase_deficiency|MAT1A-related_disorder": 1,
    "MAT1A-related_disorder|Inborn_genetic_diseases|Hepatic_methionine_adenosyltransferase_deficiency": 1,
    "Hepatic_methionine_adenosyltransferase_deficiency|not_specified|not_provided": 2,
    "MAT1A-related_disorder": 1,
    "Inborn_genetic_diseases|Hepatic_methionine_adenosyltransferase_deficiency|not_provided": 1,
    "See_cases|Hepatic_methionine_adenosyltransferase_deficiency": 1,
    "Aganglionic_megacolon|not_provided|not_specified": 1,
    "Cone-rod_dystrophy_15|not_provided": 33,
    "Cone-rod_dystrophy_15": 83,
    "Cone-rod_dystrophy_15|not_provided|not_specified": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_15|Retinitis_pigmentosa|CDHR1-related_disorder|not_provided": 1,
    "CDHR1-related_disorder|not_provided": 7,
    "not_provided|CDHR1-related_disorder|Cone-rod_dystrophy_15": 1,
    "CDHR1-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Cone-rod_dystrophy_15|CDHR1-related_disorder|not_provided": 1,
    "not_provided|CDHR1-related_disorder": 5,
    "Cone-Rod_Dystrophy|_Recessive|not_provided": 4,
    "Cone-Rod_Dystrophy|_Recessive|CDHR1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Cone-Rod_Dystrophy|_Recessive": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_15": 2,
    "not_specified|Cone-Rod_Dystrophy|_Recessive|not_provided": 3,
    "Retinitis_pigmentosa_65|not_provided|Retinal_dystrophy": 1,
    "not_specified|Cone-Rod_Dystrophy|_Recessive|not_provided|Cone-rod_dystrophy_15": 1,
    "Cone-rod_dystrophy_15|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis": 1,
    "CDHR1-related_disorder|Cone-Rod_Dystrophy|_Recessive|not_provided|Cone-rod_dystrophy_15": 1,
    "not_provided|Cone-rod_dystrophy_15": 16,
    "Retinal_dystrophy|Cone-rod_dystrophy_15|not_provided": 6,
    "Cone-rod_dystrophy_15|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy_15": 1,
    "Cone-Rod_Dystrophy|_Recessive|not_provided|not_specified": 2,
    "Retinal_dystrophy|CDHR1-related_disorder|Macular_dystrophy|_retinal|_5|Cone-Rod_Dystrophy|_Recessive|Optic_atrophy|not_specified|Cone-rod_dystrophy_15|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_65": 1,
    "Macular_dystrophy|_retinal|_5|Cone-rod_dystrophy_15|Retinitis_pigmentosa": 1,
    "CDHR1-related_disorder|Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy_15": 1,
    "Cone-rod_dystrophy_15|CDHR1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Cone-rod_dystrophy_15": 1,
    "Cone-rod_dystrophy_15|CDHR1-related_disorder|Cone-Rod_Dystrophy|_Recessive|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_65": 2,
    "not_provided|Cone-rod_dystrophy_15|Retinal_dystrophy": 2,
    "CDHR1-related_disorder|not_provided|Cone-rod_dystrophy_15": 1,
    "CDHR1-related_disorder|not_specified|Cone-rod_dystrophy_15|not_provided": 1,
    "Cone-rod_dystrophy_15|not_provided|Cone-rod_dystrophy": 2,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_15|not_provided": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_65|Cone-rod_dystrophy_15|not_provided|Retinal_dystrophy": 1,
    "not_specified|Cone-rod_dystrophy_15|not_provided": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_15": 1,
    "Cone-Rod_Dystrophy|_Recessive|not_specified|not_provided": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_15|CDHR1-related_disorder": 1,
    "Cone-Rod_Dystrophy|_Recessive|not_provided|Cone-rod_dystrophy_15|not_specified": 1,
    "CDHR1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Cone-rod_dystrophy_15|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|CDHR1-related_disorder": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_15|Retinal_dystrophy": 1,
    "Macular_dystrophy|_retinal|_5": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_15": 1,
    "Cone-Rod_Dystrophy|_Recessive|not_specified|not_provided|Cone-rod_dystrophy_15": 1,
    "not_provided|Cone-rod_dystrophy_15|Cone-Rod_Dystrophy|_Recessive": 1,
    "Macular_dystrophy|_retinal|_5|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_65|Cone-rod_dystrophy_15|Cone_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_15|CDHR1-related_disorder": 1,
    "not_provided|Cone-Rod_Dystrophy|_Recessive|not_specified": 1,
    "CDHR1-related_disorder": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|not_specified": 2,
    "Retinitis_pigmentosa_44|not_provided|not_specified|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_44|not_provided": 2,
    "RGR-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_44|not_provided|not_specified": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_44|Cone_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_44|Retinitis_pigmentosa|not_specified": 1,
    "not_specified|Retinitis_pigmentosa_44|not_provided": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_44|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|RGR-related_disorder": 2,
    "Retinitis_pigmentosa_44": 4,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|RGR-related_disorder": 1,
    "RGR-related_disorder": 1,
    "RGR-related_disorder|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_44": 1,
    "Retinitis_pigmentosa_44|not_specified|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_44": 1,
    "GRID1-associated_neurodevelopmental_disorder": 23,
    "not_specified|GRID1-associated_neurodevelopmental_disorder": 5,
    "GRID1-associated_neurodevelopmental_disorder|not_specified": 4,
    "GRID1-related_disorder": 2,
    "WAPL-related_disorder": 1,
    "Ventricular_septal_defect|Macrocephaly_at_birth|Clubfoot|Large_for_gestational_age|Polyhydramnios|Abnormality_of_the_outer_ear": 1,
    "not_provided|not_specified|Left_ventricular_noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_Myopathy|_Dominant|Myofibrillar_myopathy_4": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Myofibrillar_Myopathy|_Dominant": 1,
    "Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|not_provided|Myofibrillar_myopathy_4|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 14,
    "Myofibrillar_myopathy_4": 505,
    "Myofibrillar_myopathy_4|not_specified": 12,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_4": 13,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 2,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype": 73,
    "Myofibrillar_myopathy_4|not_provided": 18,
    "Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4": 66,
    "CARDIOMYOPATHY|_DILATED|_2L|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Primary_familial_dilated_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_4": 26,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 6,
    "Myofibrillar_myopathy_4|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided": 11,
    "not_specified|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 5,
    "not_specified|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Myofibrillar_myopathy_4": 16,
    "not_provided|not_specified|Myofibrillar_myopathy_4": 4,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Myofibrillar_myopathy_4|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_4": 10,
    "LDB3-related_disorder|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|Cardiovascular_phenotype": 1,
    "LDB3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 5,
    "not_specified|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 5,
    "Myofibrillar_myopathy_4|not_specified|Cardiovascular_phenotype": 3,
    "Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "not_provided|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 9,
    "not_provided|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 4,
    "Myofibrillar_myopathy_4|not_provided|not_specified": 3,
    "not_provided|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 14,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_4|not_provided": 2,
    "Hypertrophic_cardiomyopathy_1|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_4|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|not_provided|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Cardiomyopathy": 1,
    "not_provided|Myofibrillar_myopathy_4|not_specified": 5,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_specified": 3,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_specified": 1,
    "Cardiovascular_phenotype|LDB3-related_disorder|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|not_provided|Cardiomyopathy": 2,
    "not_provided|not_specified|Myofibrillar_myopathy_4|Cardiovascular_phenotype|Dilated_cardiomyopathy_1C": 1,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_provided": 8,
    "not_provided|LDB3-related_disorder|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_specified": 5,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_specified": 3,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|LDB3-related_disorder": 1,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided|Cardiovascular_phenotype": 3,
    "LDB3-related_disorder": 3,
    "Cardiovascular_phenotype|not_provided|not_specified|Myofibrillar_myopathy_4|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "LDB3-related_disorder|Myofibrillar_myopathy_4|not_provided|Cardiovascular_phenotype": 2,
    "not_specified|LDB3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided": 1,
    "Cardiomyopathy|Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "LDB3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Myofibrillar_myopathy_4": 6,
    "Myofibrillar_myopathy_4|not_specified|Cardiomyopathy|not_provided": 1,
    "Myofibrillar_myopathy_4|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 2,
    "Dilated_cardiomyopathy_1C|not_specified|not_provided|LDB3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Familial_hypertrophic_cardiomyopathy_24|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_specified|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1C": 14,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_specified|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_4|not_provided|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "not_provided|not_specified|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 2,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "LDB3-related_disorder|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided|not_specified": 1,
    "Dilated_cardiomyopathy_1C|not_specified|not_provided": 1,
    "not_provided|Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_4|not_specified": 1,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 8,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided": 2,
    "not_provided|not_specified|Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "not_specified|not_provided|Myofibrillar_myopathy_4": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "Myofibrillar_myopathy_4|not_specified|not_provided": 2,
    "Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "Dilated_cardiomyopathy_1C|Cardiomyopathy": 1,
    "LDB3-related_disorder|not_provided|Myofibrillar_myopathy_4": 1,
    "Left_ventricular_noncompaction_1|not_provided|Myofibrillar_myopathy_4": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_4|Cardiomyopathy": 1,
    "LDB3-related_disorder|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_specified": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_4|not_specified": 1,
    "not_specified|Myofibrillar_myopathy_4|not_provided": 3,
    "LDB3-related_disorder|Cardiovascular_phenotype|Neuromuscular_disease|Myofibrillar_myopathy|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "LDB3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_specified|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "Myofibrillar_myopathy_4|Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant": 3,
    "not_specified|Myofibrillar_myopathy_4|Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Dilated_cardiomyopathy_1C": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Myofibrillar_Myopathy|_Dominant|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided|not_specified": 1,
    "not_provided|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|not_provided|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "not_provided|Myofibrillar_myopathy_4|Cardiovascular_phenotype|Dilated_cardiomyopathy_1C": 1,
    "Cardiovascular_phenotype|not_specified|LDB3-related_disorder|not_provided|Myofibrillar_myopathy_4": 1,
    "not_provided|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Myofibrillar_Myopathy|_Dominant|not_provided|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_specified": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_specified": 2,
    "CARDIOMYOPATHY|_DILATED|_2L": 2,
    "Dilated_cardiomyopathy_1C|not_provided|not_specified": 1,
    "not_specified|Myofibrillar_myopathy_4|not_provided|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_4|Myofibrillar_myopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_specified|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_4|LDB3-related_disorder": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_specified|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|LDB3-related_disorder|Myofibrillar_myopathy_4|not_provided": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 2,
    "Myofibrillar_myopathy_4|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 2,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_Myopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Myofibrillar_myopathy_4": 1,
    "Myofibrillar_Myopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myofibrillar_myopathy_4|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "Cardiomyopathy|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 2,
    "LDB3-related_disorder|not_provided|not_specified|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "not_provided|Myofibrillar_myopathy_4|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|LDB3-related_disorder|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "LDB3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_4|not_specified": 1,
    "LDB3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|not_specified|Myofibrillar_myopathy_4": 1,
    "LDB3-related_disorder|not_specified|Myofibrillar_myopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1A|Cardiomyopathy": 1,
    "Myofibrillar_myopathy_4|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "not_provided|Myofibrillar_myopathy_4|LDB3-related_disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiomyopathy|not_specified|not_provided|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Cardiomyopathy|not_provided": 1,
    "not_provided|LDB3-related_disorder|Dilated_cardiomyopathy_1C|not_specified|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided": 1,
    "CARDIOMYOPATHY|_DILATED|_2L|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "not_provided|Dilated_cardiomyopathy_1A|Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_specified|not_provided": 1,
    "not_specified|not_provided|LDB3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "LDB3-related_disorder|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Myofibrillar_myopathy_4": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_2|Cardiomyopathy": 1,
    "not_provided|not_specified|LDB3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_4": 1,
    "Hypertrophic_cardiomyopathy_2|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|not_specified": 1,
    "Myofibrillar_myopathy_4|Isolated_Noncompaction_of_the_Ventricular_Myocardium": 1,
    "Left_ventricular_noncompaction_1": 347,
    "Myofibrillar_myopathy_4|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|LDB3-related_disorder": 2,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided|not_specified": 1,
    "not_provided|Myofibrillar_myopathy_4|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_4|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Long_QT_syndrome|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided|Dilated_cardiomyopathy_1C": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|Myofibrillar_myopathy_4|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Myofibrillar_myopathy_4|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4": 1,
    "Myofibrillar_myopathy_4|LDB3-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|Myofibrillar_myopathy_4|not_provided": 1,
    "Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_4": 2,
    "Cardiovascular_phenotype|Familial_isolated_dilated_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Myofibrillar_myopathy_4|Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "CARDIOMYOPATHY|_DILATED|_2L|Myofibrillar_myopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|Familial_isolated_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|LDB3-related_disorder|Cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_4|not_specified|Cardiovascular_phenotype|LDB3-related_disorder": 1,
    "Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|LDB3-related_disorder|Myofibrillar_myopathy_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|Familial_hypertrophic_cardiomyopathy_24|not_specified|not_provided": 1,
    "not_specified|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4": 2,
    "LDB3-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|not_provided|Left_ventricular_noncompaction_3": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C|Myofibrillar_myopathy_4|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C|Cardiomyopathy|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Myofibrillar_myopathy_4": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1C": 1,
    "not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_4|Dilated_cardiomyopathy_1C": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli": 47,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis_syndrome": 1328,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 1,
    "Juvenile_polyposis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 11,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 17,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 309,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 366,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 2,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 9,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 36,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 17,
    "Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 4,
    "Juvenile_polyposis_syndrome|not_provided|BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 6,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 2,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 19,
    "BMPR1A-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 10,
    "not_provided|Juvenile_polyposis_syndrome": 16,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 9,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided|Polyposis_syndrome|_hereditary_mixed|_2|BMPR1A-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 12,
    "not_specified|not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_provided": 23,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided": 3,
    "Polyposis_syndrome|_hereditary_mixed|_2": 17,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 3,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X": 1,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 20,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|not_provided|Malignant_tumor_of_breast|BMPR1A-related_disorder": 1,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome": 9,
    "not_provided|BMPR1A-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Pulmonary_arterial_hypertension|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided|Familial_colorectal_cancer_type_X": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome": 12,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Polyposis_syndrome|_hereditary_mixed|_2": 4,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "not_provided|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided": 2,
    "Familial_colorectal_cancer_type_X": 7,
    "Pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_arterial_hypertension_associated_with_another_disease|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome": 7,
    "not_specified|not_provided|Juvenile_polyposis_syndrome": 2,
    "not_specified|Juvenile_polyposis_syndrome": 9,
    "Juvenile_polyposis_syndrome|not_provided|not_specified": 1,
    "not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "BMPR1A-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 5,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified": 7,
    "Juvenile_polyposis_syndrome|not_specified": 13,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 7,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome": 7,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 2,
    "Polyposis_syndrome|_hereditary_mixed|_2|not_specified|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Juvenile_polyposis_syndrome": 1,
    "not_specified|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 13,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "not_specified|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Juvenile_polyposis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hand_oligodactyly|Aplasia/Hypoplasia_of_the_phalanges_of_the_hand|Palpitations|Aplasia/Hypoplasia_involving_the_metacarpal_bones|Juvenile_polyposis_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome": 4,
    "BMPR1A-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided": 12,
    "BMPR1A-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|not_provided|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|BMPR1A-related_disorder|not_specified|Juvenile_polyposis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_specified": 2,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|not_specified": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Juvenile_polyposis_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Juvenile_polyposis_syndrome|Ovarian_cancer": 1,
    "not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified": 2,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis_syndrome|not_specified|Polyposis_syndrome|_hereditary_mixed|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 1,
    "not_specified|Juvenile_polyposis_syndrome|not_provided|Polyposis_syndrome|_hereditary_mixed|_2|BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BMPR1A-Related_Polyposis_Syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BMPR1A-related_disorder|Juvenile_polyposis_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|not_provided|Hereditary_cancer-predisposing_syndrome|BMPR1A-related_disorder|Juvenile_polyposis_syndrome": 1,
    "not_provided|Carcinoma_of_colon|Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 3,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Pulmonary_arterial_hypertension": 1,
    "BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|not_specified": 1,
    "Juvenile_polyposis_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|BMPR1A-related_disorder|Juvenile_polyposis_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|not_provided": 1,
    "Pulmonary_arterial_hypertension|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified|BMPR1A-related_disorder|Pulmonary_arterial_hypertension|Familial_colorectal_cancer_type_X|Juvenile_polyposis_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided": 1,
    "Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2": 2,
    "Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided": 3,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2": 2,
    "Polyposis_syndrome|_hereditary_mixed|_2|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "not_provided|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Pulmonary_arterial_hypertension": 1,
    "Juvenile_polyposis_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Pulmonary_arterial_hypertension": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Pulmonary_arterial_hypertension": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Pulmonary_arterial_hypertension|Juvenile_polyposis_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Pulmonary_arterial_hypertension|not_provided|BMPR1A-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Gastrointestinal_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Malignant_tumor_of_breast": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_meningioma": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Pulmonary_arterial_hypertension": 1,
    "BMPR1A-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|not_provided|not_specified": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|BMPR1A-related_disorder": 1,
    "Juvenile_polyposis_syndrome|Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified": 1,
    "BMPR1A-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|Carcinoma_of_colon": 1,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_Polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Juvenile_polyposis_syndrome": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|not_specified": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Pulmonary_arterial_hypertension|not_provided": 1,
    "BMPR1A-related_disorder|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|BMPR1A-related_disorder|not_specified|not_provided|Juvenile_polyposis_syndrome": 1,
    "not_provided|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli|BMPR1A-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Pulmonary_arterial_hypertension|Idiopathic_and/or_familial_pulmonary_arterial_hypertension|Juvenile_polyposis_syndrome": 1,
    "BMPR1A-related_disorder|not_provided|Juvenile_polyposis_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|not_specified|not_provided": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|not_provided": 1,
    "Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2|Hereditary_cancer-predisposing_syndrome|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|not_provided|not_specified": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|not_provided|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|B_lymphoblastic_leukemia_lymphoma_with_t(12%3B21)(p13%3Bq22)%3B_TEL-AML1_(ETV6-RUNX1)": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided|Juvenile_polyposis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Polyposis_syndrome|_hereditary_mixed|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Pulmonary_arterial_hypertension": 1,
    "Juvenile_Polyposis": 1,
    "Polyposis_syndrome|_hereditary_mixed|_2|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 1,
    "not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 3,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 1,
    "Hyperinsulinism-hyperammonemia_syndrome": 138,
    "Hyperinsulinism-hyperammonemia_syndrome|GLUD1-related_disorder": 2,
    "GLUD1-related_disorder|Inborn_genetic_diseases|Hyperinsulinism-hyperammonemia_syndrome": 2,
    "Hyperinsulinism-hyperammonemia_syndrome|Inborn_genetic_diseases": 6,
    "Familial_hyperinsulinemia|Hyperinsulinism-hyperammonemia_syndrome|not_provided": 1,
    "not_provided|Hyperinsulinism-hyperammonemia_syndrome": 5,
    "Inborn_genetic_diseases|Hyperinsulinism-hyperammonemia_syndrome": 2,
    "Hyperinsulinism-hyperammonemia_syndrome|not_specified": 2,
    "not_specified|Hyperinsulinism-hyperammonemia_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hyperinsulinism-hyperammonemia_syndrome|not_provided": 4,
    "not_provided|Hyperinsulinism|_Dominant|Hyperinsulinism-hyperammonemia_syndrome|not_specified": 1,
    "Hyperinsulinism-hyperammonemia_syndrome|not_provided": 4,
    "Hyperinsulinism-hyperammonemia_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "GLUD1-related_disorder": 8,
    "Intellectual_disability|Hyperinsulinism-hyperammonemia_syndrome": 1,
    "not_specified|Hyperinsulinism-hyperammonemia_syndrome": 4,
    "Inborn_genetic_diseases|not_specified|not_provided|GLUD1-related_disorder": 1,
    "Hyperinsulinism-hyperammonemia_syndrome|Familial_hyperinsulinism": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hyperinsulinism-hyperammonemia_syndrome": 1,
    "Hyperinsulinism-hyperammonemia_syndrome|GLUD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Hyperinsulinism-hyperammonemia_syndrome|GLUD1-related_disorder": 2,
    "not_provided|not_specified|Hyperinsulinism-hyperammonemia_syndrome": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Hyperinsulinism-hyperammonemia_syndrome": 1,
    "not_provided|GLUD1-related_disorder|Hyperinsulinism-hyperammonemia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hyperinsulinism-hyperammonemia_syndrome|not_specified|not_provided": 1,
    "not_provided|Monogenic_diabetes|Hyperinsulinism-hyperammonemia_syndrome|not_specified": 1,
    "not_provided|Hyperinsulinism-hyperammonemia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Monogenic_diabetes|Hyperinsulinism-hyperammonemia_syndrome": 1,
    "GLUD1-related_disorder|Inborn_genetic_diseases|not_specified|Hyperinsulinism-hyperammonemia_syndrome": 1,
    "Pontocerebellar_hypoplasia|_type_16": 18,
    "Thyroid_cancer|_nonmedullary|_2": 7,
    "Pontocerebellar_hypoplasia|_type_16|Thyroid_cancer|_nonmedullary|_2": 3,
    "not_provided|MINPP1-related_disorder": 1,
    "MINPP1-related_disorder": 3,
    "Thyroid_adenoma|not_provided": 1,
    "Pontocerebellar_hypoplasia|_type_16|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 202,
    "not_provided|not_specified|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 3,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 11,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|PAPSS2-related_disorder|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_provided": 7,
    "PAPSS2-related_disorder|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|Brachyolmia": 1,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|PAPSS2-related_disorder": 5,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|Inborn_genetic_diseases": 14,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_specified": 2,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_specified": 1,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_provided|not_specified": 1,
    "not_specified|not_provided|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 1,
    "Skeletal_dysplasia|not_provided|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 1,
    "PAPSS2-related_disorder|not_specified|not_provided|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type": 1,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_specified|not_provided": 1,
    "Autosomal_recessive_brachyolmia|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_provided": 1,
    "PAPSS2-related_disorder|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_provided": 1,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_PAPSS2_type|not_provided|Inborn_genetic_diseases": 1,
    "ATAD1-related_disorder": 2,
    "Hyperekplexia_4|not_provided": 1,
    "not_provided|Hyperekplexia_4": 2,
    "Hyperekplexia_4|Inborn_genetic_diseases|not_provided": 1,
    "Hyperekplexia_4|not_provided|ATAD1-related_disorder": 1,
    "Hyperekplexia_4": 2,
    "Inborn_genetic_diseases|not_provided|Hyperekplexia_4": 1,
    "Cowden_syndrome_4": 3,
    "not_specified|not_provided|KLLN-related_disorder": 1,
    "not_specified|not_provided|KLLN-related_disorder|Cowden_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome": 732,
    "KLLN-related_disorder": 2,
    "not_provided|PTEN_hamartoma_tumor_syndrome": 62,
    "not_provided|Familial_meningioma|Prostate_cancer|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_specified|Cowden_syndrome_4": 1,
    "not_provided|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Prostate_cancer|Cowden_syndrome_1|Familial_meningioma": 1,
    "PTEN-related_disorder|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 33,
    "PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|Familial_meningioma|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Prostate_cancer|PTEN-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder|not_provided|Macrocephaly-autism_syndrome|Familial_meningioma|Prostate_cancer|Glioma_susceptibility_2": 1,
    "KLLN-related_disorder|not_provided": 1,
    "not_provided|PTEN-related_disorder": 3,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_4|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder": 23,
    "Glioma_susceptibility_2|Cowden_syndrome_1|Familial_meningioma|Prostate_cancer|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Cowden_syndrome_1|Glioma_susceptibility_2|Familial_prostate_cancer|not_provided": 1,
    "Familial_meningioma|Glioma_susceptibility_2|Prostate_cancer|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cowden_syndrome_4|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Cowden_syndrome_4|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Seizure": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Macrocephaly-autism_syndrome|Prostate_cancer|VACTERL_with_hydrocephalus|Cowden_syndrome_1|Glioma_susceptibility_2|Familial_meningioma|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder": 1,
    "PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2": 1,
    "Prostate_cancer|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|PTEN_hamartoma_tumor_syndrome": 2,
    "not_provided|Macrocephaly-autism_syndrome|Familial_meningioma|Cowden_syndrome_1|Glioma_susceptibility_2|Familial_prostate_cancer|not_specified": 1,
    "Macrocephaly-autism_syndrome|Prostate_cancer|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_meningioma|Familial_prostate_cancer|Glioma_susceptibility_2|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 44,
    "Macrocephaly-autism_syndrome|Familial_meningioma|Prostate_cancer|Cowden_syndrome_1|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Bannayan-Riley-Ruvalcaba_syndrome|Cowden_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "Familial_meningioma|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Familial_prostate_cancer|Cowden_syndrome_1|PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Familial_meningioma|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Prostate_cancer|Cowden_syndrome_1|not_provided": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome": 8,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|Prostate_cancer|Familial_meningioma|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|VACTERL_with_hydrocephalus|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Cowden_syndrome_1|Prostate_cancer|Glioma_susceptibility_2": 1,
    "Familial_meningioma|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Prostate_cancer|Cowden_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome_1": 1,
    "not_specified|not_provided|Cowden_syndrome_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 3,
    "Cowden_syndrome|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Bannayan-Riley-Ruvalcaba_syndrome": 1,
    "Macrocephaly-autism_syndrome|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Prostate_cancer|Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|not_provided": 1,
    "Familial_prostate_cancer|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Familial_meningioma|Glioma_susceptibility_2": 2,
    "PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome": 3,
    "PTEN-related_disorder|Hereditary_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome|PTEN-related_disorder|not_provided|Familial_meningioma|Glioma_susceptibility_2|Familial_prostate_cancer|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Myeloproliferative_neoplasm|_unclassifiable": 1,
    "PTEN-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1": 1,
    "PTEN-related_disorder|not_specified": 1,
    "Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 4,
    "PTEN_hamartoma_tumor_syndrome|not_specified": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTEN-related_disorder|not_specified": 1,
    "Cowden_syndrome_1|not_specified|not_provided": 1,
    "Myeloproliferative_neoplasm|_unclassifiable": 2,
    "PTEN-related_disorder|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_meningioma|Cowden_syndrome_1|Glioma_susceptibility_2|Familial_prostate_cancer|Macrocephaly-autism_syndrome": 1,
    "Hamartomatous_polyposis": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Prostate_cancer|Cowden_syndrome_1": 1,
    "not_specified|PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_provided": 1,
    "not_specified|PTEN-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 26,
    "not_provided|Glioma_susceptibility_2": 2,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Glioma_susceptibility_2|Cowden_syndrome_1|Familial_meningioma|Macrocephaly-autism_syndrome|Familial_prostate_cancer": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided": 41,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 147,
    "PTEN_hamartoma_tumor_syndrome|Malignant_tumor_of_breast|Cowden_syndrome_1|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 12,
    "not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_specified|Cowden_syndrome_1": 3,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 138,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 22,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 31,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 2,
    "not_provided|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 12,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 33,
    "developmental_delay_with_seizures": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 20,
    "PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome": 1,
    "not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_provided": 1,
    "Cowden_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome": 10,
    "Cowden_syndrome_1|Macrocephaly-autism_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_provided|PTEN_hamartoma_tumor_syndrome": 2,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 22,
    "not_specified|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Glioma_susceptibility_2": 11,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Familial_prostate_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 12,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 6,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 15,
    "Melanoma|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 43,
    "not_provided|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|not_specified|PTEN_hamartoma_tumor_syndrome|Glioma|not_provided": 1,
    "Cowden_syndrome_1|PTEN-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 14,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Malignant_tumor_of_breast|not_provided": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|See_cases|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified|PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 13,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_of_infancy|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 71,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome_1": 3,
    "Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified": 3,
    "Neurodevelopmental_delay|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided": 4,
    "not_provided|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Macrocephaly-autism_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Macrocephaly": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided": 16,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Malignant_tumor_of_breast|not_specified|PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Malignant_tumor_of_breast": 2,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_provided": 4,
    "Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|not_specified": 1,
    "Bannayan-Riley-Ruvalcaba_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 12,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided": 2,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Uterine_corpus_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Familial_prostate_cancer|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndromes|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Vater_association_with_macrocephaly_and_ventriculomegaly": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN-related_disorder|Hereditary_cancer": 1,
    "PTEN_hamartoma_tumor_syndrome|See_cases|not_provided": 1,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 4,
    "Prostate_cancer|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Cowden_syndrome_1|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Breast_carcinoma": 1,
    "Cowden_syndrome_1|Prostate_cancer|Familial_meningioma|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Endometrial_carcinoma|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Familial_meningioma|not_provided|Glioma_susceptibility_2|Prostate_cancer|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_meningioma|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 4,
    "Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder": 3,
    "Cowden_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Familial_cancer_of_breast": 1,
    "PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Cowden_syndrome_1|Familial_prostate_cancer|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Carcinoma_of_colon|not_provided": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_specified": 2,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Familial_meningioma|Familial_prostate_cancer|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified": 1,
    "Familial_meningioma|Familial_prostate_cancer|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_meningioma|Familial_prostate_cancer|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|not_provided": 12,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|not_specified|Cowden_syndrome_1|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|not_provided|Familial_meningioma|Glioma_susceptibility_2|Prostate_cancer|Breast_and/or_ovarian_cancer": 1,
    "PTEN_hamartoma_tumor_syndrome|Breast_neoplasm": 1,
    "Endometrial_carcinoma|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided|Macrocephaly-autism_syndrome|Cowden_syndrome_1": 1,
    "Familial_meningioma|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Prostate_cancer|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|PTEN-related_disorder": 1,
    "PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 3,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_specified": 1,
    "not_provided|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_specified|not_provided": 1,
    "Macrocephaly-autism_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|PTEN-related_disorder|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Loss_of_consciousness|Macrocephaly|Large_for_gestational_age": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Cowden_syndrome_1|Familial_meningioma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_meningioma|Familial_prostate_cancer|Glioma_susceptibility_2|Cowden_syndrome_1|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Bannayan-Riley-Ruvalcaba_syndrome|not_provided": 1,
    "Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_provided": 1,
    "Seizure|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_1": 11,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Endometrial_hyperplasia_without_atypia|Atypical_endometrial_hyperplasia": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_1|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|Lhermitte-Duclos_disease": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Prostate_cancer|_hereditary|_1": 6,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Familial_meningioma|Macrocephaly-autism_syndrome|Familial_prostate_cancer": 1,
    "PTEN_hamartoma_tumor_syndrome|Familial_meningioma": 1,
    "not_provided|Prostate_cancer|_hereditary|_1": 29,
    "Prostate_cancer|_hereditary|_1|not_provided": 20,
    "PTEN-related_disorder|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_1": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Autism|Macrocephaly|Bannayan-Riley-Ruvalcaba_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|PTEN_hamartoma_tumor_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 3,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Endometrial_carcinoma": 1,
    "Familial_meningioma|Familial_prostate_cancer|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Cowden_syndrome_1|PTEN-related_disorder|Prostate_cancer|Gastric_cancer|Cowden_syndrome|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|PTEN_hamartoma_tumor_syndrome|Abnormal_cardiovascular_system_morphology": 1,
    "PTEN-related_disorder|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_specified|not_provided|PTEN-related_disorder": 1,
    "Cowden_syndrome_1|Prostate_cancer|_hereditary|_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Ovarian_neoplasm|Cowden_syndrome_1": 1,
    "Glioma_susceptibility_2|Familial_meningioma|Prostate_cancer|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome|not_provided": 1,
    "Glioma|Cowden_syndrome|Mediastinal_germ_cell_tumor|Acute_megakaryoblastic_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2": 1,
    "PTEN_hamartoma_tumor_syndrome|Malignant_tumor_of_urinary_bladder|not_provided|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Macrocephaly-autism_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 3,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurodevelopmental_delay|Autistic_behavior|Macrocephaly": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome": 21,
    "PTEN_hamartoma_tumor_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Glioma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|PTEN_hamartoma_tumor_syndrome|Carcinoma_of_colon|Cowden_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_1|Cowden_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Macrocephaly-autism_syndrome|Cowden_syndrome_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndromes|Macrocephaly-autism_syndrome|Cowden_syndrome_1|not_provided|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Papillary_tumor_of_the_pineal_region": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Lhermitte-Duclos_disease": 1,
    "Prostate_cancer|_hereditary|_1|Cowden_syndrome_1": 1,
    "Bannayan-Riley-Ruvalcaba_syndrome": 1,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|PTEN_hamartoma_tumor_syndromes|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|not_provided|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|Familial_meningioma|Prostate_cancer|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Cowden_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|not_specified|PTEN_hamartoma_tumor_syndrome": 1,
    "not_specified|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 6,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "Macrocephaly-autism_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|Proteus-like_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "Cowden_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome|PTEN_hamartoma_tumor_syndrome": 2,
    "Cowden_syndrome_1|not_provided|PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Macrocephaly-autism_syndrome|Prostate_cancer|Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Macrocephaly-autism_syndrome|VACTERL_with_hydrocephalus|Cowden_syndrome_1|Prostate_cancer|Familial_meningioma|Glioma_susceptibility_2|Malignant_lymphoma|_large_B-cell|_diffuse|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Neurodevelopmental_delay|not_provided": 1,
    "not_specified|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|not_specified|not_provided": 1,
    "PTEN-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_provided": 2,
    "Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Bannayan-Riley-Ruvalcaba_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Neurodevelopmental_abnormality|PTEN_hamartoma_tumor_syndrome": 1,
    "Prostate_cancer|_somatic|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|Glioma_susceptibility_2|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Malignant_tumor_of_breast": 1,
    "See_cases|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Prostate_cancer|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Familial_meningioma|Cowden_syndrome_1": 1,
    "not_provided|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|not_provided|Macrocephaly-autism_syndrome|Familial_meningioma|Familial_prostate_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder|Melanoma|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Familial_meningioma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Bannayan-Riley-Ruvalcaba_syndrome|Proteus-like_syndrome|Cowden_syndrome|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Prostate_cancer|Cowden_syndrome_1|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided|Intellectual_disability": 1,
    "not_specified|Cowden_syndrome_1": 3,
    "not_specified|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|not_provided|PTEN_hamartoma_tumor_syndrome": 2,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Cowden_syndrome_1|not_provided": 1,
    "Melanoma|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Familial_prostate_cancer|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|PTEN-related_disorder|Cowden_syndrome_1": 1,
    "Thyroid_cancer|_nonmedullary|_2|Cowden_syndrome_1": 1,
    "Hemangioma|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2": 1,
    "PTEN-related_disorder|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Ovarian_neoplasm|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Abnormal_cardiovascular_system_morphology": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|not_provided|Meningioma|Macrocephaly-autism_syndrome": 1,
    "Inborn_genetic_diseases|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Macrocephaly-autism_syndrome": 1,
    "not_provided|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Cowden_syndrome_1|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Familial_prostate_cancer|Familial_meningioma|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Prostate_cancer": 1,
    "Ovarian_neoplasm|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "Bannayan-Riley-Ruvalcaba_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome|not_provided|Cowden_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Atypical_endometrial_hyperplasia": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Prostate_cancer|_somatic": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder|not_provided": 1,
    "Cowden_syndrome_1|Familial_prostate_cancer|Glioma_susceptibility_2|Macrocephaly-autism_syndrome|Familial_meningioma": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|PTEN-related_disorder": 1,
    "Malignant_lymphoma|_large_B-cell|_diffuse|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "PTEN_hamartoma_tumor_syndrome|Segmental_outgrowth-lipomatosis-arteriovenous_malformation-epidermal_nevus_syndrome|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome_1|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Glioma_susceptibility_2|Familial_prostate_cancer|Familial_meningioma|Macrocephaly-autism_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|Familial_prostate_cancer|Macrocephaly-autism_syndrome|Familial_meningioma|Cowden_syndrome_1": 1,
    "PTEN_hamartoma_tumor_syndrome|not_specified|PTEN-related_disorder": 1,
    "Cowden_syndrome_1|not_specified": 4,
    "Cowden_syndrome_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|Prostate_cancer|Macrocephaly-autism_syndrome|not_specified|PTEN_hamartoma_tumor_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|Prostate_cancer|Macrocephaly-autism_syndrome|Familial_prostate_cancer": 1,
    "Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Familial_prostate_cancer|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "not_provided|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|PTEN_hamartoma_tumor_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder|Cowden_syndrome_1|not_specified": 1,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|Cowden_syndrome_1|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|not_specified": 1,
    "Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Familial_meningioma|Familial_prostate_cancer|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_provided|PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "PTEN-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Cowden_syndrome_1|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Familial_prostate_cancer|PTEN_hamartoma_tumor_syndrome": 1,
    "Breast_and/or_ovarian_cancer|PTEN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|Macrocephaly-autism_syndrome|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Bannayan-Riley-Ruvalcaba_syndrome": 1,
    "Glioma_susceptibility_2|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Familial_meningioma|Familial_prostate_cancer|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Macrocephaly-autism_syndrome|Familial_meningioma|Prostate_cancer|VACTERL_with_hydrocephalus|Cowden_syndrome_1|Glioma_susceptibility_2": 1,
    "PTEN_hamartoma_tumor_syndrome|not_provided|Cowden_syndrome_1": 1,
    "Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PTEN-related_disorder|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Cowden_syndrome_1|See_cases|PTEN_hamartoma_tumor_syndrome|not_provided|Macrocephaly-autism_syndrome|PTEN-related_disorder|Glioma_susceptibility_2|Prostate_cancer|Familial_meningioma": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_provided": 1,
    "not_provided|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|not_provided|PTEN-related_disorder": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Glioma_susceptibility_2|Familial_meningioma|Cowden_syndrome_1|Familial_prostate_cancer|Macrocephaly-autism_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Familial_ovarian_cancer|not_provided|Bannayan-Riley-Ruvalcaba_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Endometrial_carcinoma|Macrocephaly-autism_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Prostate_cancer|Thyroid_cancer|_nonmedullary|_2|Familial_meningioma|VACTERL_with_hydrocephalus|PTEN-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_provided|Macrocephaly-autism_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|PTEN-related_disorder|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|PTEN-related_disorder": 1,
    "not_provided|Macrocephaly-autism_syndrome|VACTERL_with_hydrocephalus|PTEN_hamartoma_tumor_syndrome|Familial_meningioma|Glioma_susceptibility_2|Cowden_syndrome_1|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|PTEN-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN-related_disorder|Cowden_syndrome_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|PTEN-related_disorder|Familial_meningioma|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Cowden_syndrome_1|Prostate_cancer|not_specified|not_provided": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Familial_meningioma|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Familial_prostate_cancer": 1,
    "Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|not_provided|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Cowden_syndrome_1|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Cowden_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|not_provided|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Cowden_syndrome_1": 1,
    "Familial_prostate_cancer|Glioma_susceptibility_2|Cowden_syndrome_1|Familial_meningioma|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Familial_cancer_of_breast|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome": 1,
    "Malignant_lymphoma|_large_B-cell|_diffuse|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|PTEN-related_disorder": 1,
    "Macrocephaly-autism_syndrome|Cowden_syndrome|PTEN-related_disorder|Cowden_syndrome_1|Glioma_susceptibility_2|Prostate_cancer|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|PTEN_hamartoma_tumor_syndrome|Proteus-like_syndrome|Familial_cancer_of_breast|Abnormality_of_the_nervous_system": 1,
    "Familial_meningioma|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_1|Cowden_syndrome|not_provided|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified|Macrocephaly-autism_syndrome|Familial_meningioma|Glioma_susceptibility_2|Familial_prostate_cancer": 1,
    "Endometrial_carcinoma|Cowden_syndrome_1|Glioma_susceptibility_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|Macrocephaly-autism_syndrome|Familial_meningioma|Familial_prostate_cancer|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome": 1,
    "not_provided|Macrocephaly-autism_syndrome|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Cowden_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Ovarian_neoplasm|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Familial_prostate_cancer|Familial_meningioma|Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified|PTEN_hamartoma_tumor_syndrome": 1,
    "Breast_cancer|_susceptibility_to|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Prostate_cancer|Familial_meningioma|Macrocephaly-autism_syndrome|Cowden_syndrome_1|Glioma_susceptibility_2|PTEN-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Malignant_tumor_of_breast": 1,
    "PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Glioma_susceptibility_2|not_provided|not_specified|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "Cowden_syndrome_1|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Cowden_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|PTEN_hamartoma_tumor_syndrome|Macrocephaly-autism_syndrome|Glioma_susceptibility_2|Familial_prostate_cancer|Familial_meningioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Glioma_susceptibility_2": 1,
    "Glioma_susceptibility_2|PTEN_hamartoma_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Macrocephaly-autism_syndrome|Prostate_cancer|Cowden_syndrome_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|PTEN_hamartoma_tumor_syndrome|Cowden_syndrome_1": 1,
    "not_provided|Glioma_susceptibility_2|Hereditary_cancer-predisposing_syndrome|PTEN_hamartoma_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_1|not_specified|not_provided": 1,
    "PTEN_hamartoma_tumor_syndrome|not_specified|Breast_and/or_ovarian_cancer|Cowden_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_2|Familial_prostate_cancer|Macrocephaly-autism_syndrome|Familial_meningioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_1": 1,
    "PTEN_hamartoma_tumor_syndrome|Squamous_cell_carcinoma|Lung_adenocarcinoma": 1,
    "Family_history": 1,
    "not_provided|Stage_5_chronic_kidney_disease": 1,
    "LIPK-related_disorder": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_8": 2,
    "not_provided|LIPN-related_disorder": 1,
    "LIPN-related_disorder|not_provided": 2,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_8": 1,
    "LIPN-related_disorder": 1,
    "Autosomal_recessive_congenital_ichthyosis_8": 1,
    "Moyamoya_disease|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multisystemic_smooth_muscle_dysfunction_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Moyamoya_disease|Multisystemic_smooth_muscle_dysfunction_syndrome": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Aortic_aneurysm|_familial_thoracic_6": 6,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "ACTA2-related_disorder|Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|not_provided": 9,
    "Aortic_aneurysm|_familial_thoracic_6": 193,
    "Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "Aortic_aneurysm|_familial_thoracic_6|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "not_provided|Aortic_aneurysm|_familial_thoracic_6": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 42,
    "Aortic_aneurysm|_familial_thoracic_6|not_provided": 9,
    "Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aneurysm_of_descending_aorta|Arterial_tortuosity": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|ACTA2-related_disorder|not_specified": 1,
    "ACTA2-related_disorder|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|Multisystemic_smooth_muscle_dysfunction_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_6": 4,
    "not_provided|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "ACTA2-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 2,
    "ACTA2-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ACTA2-related_disorder|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_6": 4,
    "Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|not_specified": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_6|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|Cardiovascular_phenotype": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 4,
    "not_provided|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5|Aortic_aneurysm|_familial_thoracic_6|not_provided": 1,
    "Moyamoya_disease_5|Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multisystemic_smooth_muscle_dysfunction_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Moyamoya_disease_5": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm|ACTA2-related_disorder|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Aortic_aneurysm|_familial_thoracic_6|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome": 2,
    "Connective_tissue_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_6|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Aortic_aneurysm|_familial_thoracic_6|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multisystemic_smooth_muscle_dysfunction_syndrome|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thoracic_aortic_aneurysm_or_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|not_specified": 2,
    "not_provided|Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome": 2,
    "ACTA2-related_disorder|Connective_tissue_disorder|alterations_of_great_arteries_and_veins|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|Multisystemic_smooth_muscle_dysfunction_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Familial_aortopathy|not_provided|Multisystemic_smooth_muscle_dysfunction_syndrome": 1,
    "Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Thoracic_aortic_aneurysm_or_dissection|Aortic_aneurysm|_familial_thoracic_6": 1,
    "not_provided|Familial_aortopathy|not_specified|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Descending_aortic_dissection": 1,
    "Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|ACTA2-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease|not_provided|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Aortic_aneurysm|_familial_thoracic_6|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ACTA2-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|Connective_tissue_disorder|not_specified|Multisystemic_smooth_muscle_dysfunction_syndrome": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_6|not_provided|Thoracic_aortic_aneurysm": 1,
    "Aortic_aneurysm|_familial_thoracic_6|not_specified": 2,
    "Moyamoya_disease|Multisystemic_smooth_muscle_dysfunction_syndrome|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6": 2,
    "Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5|Cardiovascular_phenotype": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Connective_tissue_disorder|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Moyamoya_disease_5|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_6|ACTA2-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|Multisystemic_smooth_muscle_dysfunction_syndrome": 1,
    "ACTA2-related_disorder|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multisystemic_smooth_muscle_dysfunction_syndrome|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Connective_tissue_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Aortic_aneurysm|_familial_thoracic_6|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_6|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy|Aortic_aneurysm|_familial_thoracic_6": 1,
    "ACTA2-related_disorder|Aortic_aneurysm|_familial_thoracic_6|Moyamoya_disease_5|Multisystemic_smooth_muscle_dysfunction_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy|See_cases": 1,
    "not_specified|Moyamoya_disease|Aortic_aneurysm|_familial_thoracic_6|Congenital_aneurysm_of_ascending_aorta|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease_5": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ACTA2-related_disorder": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|not_provided|Aortic_aneurysm|_familial_thoracic_6": 1,
    "Aortic_aneurysm|_familial_thoracic_6|Multisystemic_smooth_muscle_dysfunction_syndrome": 2,
    "Moyamoya_disease|Multisystemic_smooth_muscle_dysfunction_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|LUNG_CANCER|_SUSCEPTIBILITY_TO": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Moyamoya_disease|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Moyamoya_disease|Multisystemic_smooth_muscle_dysfunction_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Moyamoya_disease|Multisystemic_smooth_muscle_dysfunction_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Multisystemic_smooth_muscle_dysfunction_syndrome|Autoimmune_lymphoproliferative_syndrome_type_1|Moyamoya_disease|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Moyamoya_disease|not_provided|Multisystemic_smooth_muscle_dysfunction_syndrome|Autoimmune_lymphoproliferative_syndrome_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Multisystemic_smooth_muscle_dysfunction_syndrome|Autoimmune_lymphoproliferative_syndrome_type_1|Moyamoya_disease|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Moyamoya_disease|Multisystemic_smooth_muscle_dysfunction_syndrome|Autoimmune_lymphoproliferative_syndrome_type_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|FAS-related_disorder": 3,
    "Inborn_genetic_diseases|Autoimmune_lymphoproliferative_syndrome_type_1": 6,
    "not_specified|not_provided|Autoimmune_lymphoproliferative_syndrome_type_1": 3,
    "Autoimmune_lymphoproliferative_syndrome_type_1|Inborn_genetic_diseases": 6,
    "AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IA": 9,
    "FAS-related_disorder|not_provided|not_specified|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "FAS-related_disorder|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IA": 3,
    "not_provided|FAS-related_disorder|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "SQUAMOUS_CELL_CARCINOMA|_BURN_SCAR-RELATED|_SOMATIC": 3,
    "AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IA|Autoimmune_lymphoproliferative_syndrome_type_1": 4,
    "not_specified|Autoimmune_lymphoproliferative_syndrome_type_1|not_provided": 2,
    "FAS-related_disorder|not_specified|not_provided|Autoimmune_lymphoproliferative_syndrome_type_1": 2,
    "Autoimmune_lymphoproliferative_syndrome": 1,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_1|Splenomegaly": 1,
    "not_provided|Autoimmune_lymphoproliferative_syndrome_type_1|not_specified": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_1|Hepatoblastoma": 1,
    "not_provided|Inherited_Immunodeficiency_Diseases|Autoimmune_lymphoproliferative_syndrome_type_1|See_cases": 1,
    "not_provided|AUTOIMMUNE_LYMPHOPROLIFERATIVE_SYNDROME|_TYPE_IA|Autoimmune_lymphoproliferative_syndrome_type_1": 1,
    "FAS-related_disorder": 1,
    "Wolman_disease|Lysosomal_acid_lipase_deficiency": 20,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease": 31,
    "Lysosomal_acid_lipase_deficiency": 83,
    "not_provided|Lysosomal_acid_lipase_deficiency|Wolman_disease": 2,
    "Wolman_disease": 289,
    "Wolman_disease|Cholesteryl_ester_storage_disease|Cardiovascular_phenotype": 1,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease|Cardiovascular_phenotype": 1,
    "Wolman_disease|Lysosomal_acid_lipase_deficiency|not_provided": 2,
    "Lysosomal_acid_lipase_deficiency|Cardiovascular_phenotype": 1,
    "Lysosomal_acid_lipase_deficiency|Cardiovascular_phenotype|Wolman_disease": 2,
    "not_provided|Wolman_disease|Lysosomal_acid_lipase_deficiency|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Wolman_disease|not_provided|Lysosomal_acid_lipase_deficiency": 3,
    "Lysosomal_acid_lipase_deficiency|not_provided|Wolman_disease": 1,
    "Wolman_disease|Cardiovascular_phenotype|Lysosomal_acid_lipase_deficiency": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "not_provided|LIPA-related_disorder|Wolman_disease|Cardiovascular_phenotype": 1,
    "Wolman_disease|Cardiovascular_phenotype": 35,
    "not_provided|Wolman_disease|Cardiovascular_phenotype": 4,
    "Wolman_disease|Cholesteryl_ester_storage_disease|Lysosomal_acid_lipase_deficiency": 4,
    "LIPA-related_disorder|Lysosomal_acid_lipase_deficiency|Wolman_disease|Cardiovascular_phenotype": 1,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease|Cholesteryl_ester_storage_disease": 4,
    "Cardiovascular_phenotype|Wolman_disease|LIPA-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Wolman_disease|Lysosomal_acid_lipase_deficiency": 2,
    "Cardiovascular_phenotype|not_provided|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "not_provided|Wolman_disease|Lysosomal_acid_lipase_deficiency|Cholesteryl_ester_storage_disease": 1,
    "Cardiovascular_phenotype|Wolman_disease|LIPA-related_disorder|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|Cardiovascular_phenotype|not_provided": 1,
    "Cholesteryl_ester_storage_disease|Wolman_disease|Lysosomal_acid_lipase_deficiency": 5,
    "Wolman_disease|Cardiovascular_phenotype|LIPA-related_disorder|Lysosomal_acid_lipase_deficiency": 1,
    "Cardiovascular_phenotype|not_specified|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "Cardiovascular_phenotype|Wolman_disease": 7,
    "Wolman_disease|not_provided": 6,
    "LIPA-related_disorder|Lysosomal_acid_lipase_deficiency": 1,
    "not_provided|not_specified|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|LIPA-related_disorder|not_specified|not_provided|Cholesteryl_ester_storage_disease|Lysosomal_acid_lipase_deficiency": 1,
    "Cholesteryl_ester_storage_disease": 7,
    "Cardiovascular_phenotype|Lysosomal_acid_lipase_deficiency|Wolman_disease": 1,
    "Cholesteryl_ester_storage_disease|Wolman_disease": 10,
    "not_provided|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "LIPA-related_disorder|Wolman_disease": 2,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease|not_provided": 2,
    "Cholesteryl_ester_storage_disease|Cardiovascular_phenotype|LIPA-related_disorder|Wolman_disease|not_provided|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|Cholesteryl_ester_storage_disease": 9,
    "Cardiovascular_phenotype|not_specified|not_provided|Lysosomal_acid_lipase_deficiency|Wolman_disease|LIPA-related_disorder|Cholesteryl_ester_storage_disease": 1,
    "Cardiovascular_phenotype|LIPA-related_disorder|not_provided|Wolman_disease": 1,
    "Lysosomal_acid_lipase_deficiency|Cholesteryl_ester_storage_disease|Wolman_disease": 1,
    "Cardiovascular_phenotype|not_provided|Wolman_disease": 1,
    "Cardiovascular_phenotype|Cholesteryl_ester_storage_disease|Lysosomal_acid_lipase_deficiency|Wolman_disease|not_provided": 1,
    "Cholesteryl_ester_storage_disease|Wolman_disease|not_provided|Lysosomal_acid_lipase_deficiency": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Lysosomal_acid_lipase_deficiency|Wolman_disease": 3,
    "LIPA-related_disorder|not_specified|not_provided|Cardiovascular_phenotype|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|not_provided|Cardiovascular_phenotype": 1,
    "Wolman_disease|LIPA-related_disorder|Cardiovascular_phenotype|not_provided|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|LIPA-related_disorder|Cardiovascular_phenotype": 1,
    "LIPA-related_disorder": 4,
    "Wolman_disease|Lysosomal_acid_lipase_deficiency|LIPA-related_disorder|Cholesteryl_ester_storage_disease|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Wolman_disease": 4,
    "not_specified|not_provided|Lysosomal_acid_lipase_deficiency": 1,
    "not_provided|Lysosomal_acid_lipase_deficiency": 4,
    "LIPA-related_disorder|Wolman_disease|not_provided|Cardiovascular_phenotype|Lysosomal_acid_lipase_deficiency": 1,
    "LIPA-related_disorder|Wolman_disease|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Lysosomal_acid_lipase_deficiency|not_provided": 1,
    "not_provided|Wolman_disease|Cardiovascular_phenotype|Lysosomal_acid_lipase_deficiency": 2,
    "Wolman_disease|Lysosomal_acid_lipase_deficiency|Cholesteryl_ester_storage_disease": 2,
    "Cholesteryl_ester_storage_disease|Lysosomal_acid_lipase_deficiency|Wolman_disease": 1,
    "Wolman_disease|Cholesteryl_ester_storage_disease|not_provided|LIPA-related_disorder|Lysosomal_acid_lipase_deficiency": 1,
    "LIPA-related_disorder|not_provided|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "not_specified|Wolman_disease|LIPA-related_disorder|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|not_specified|Lysosomal_acid_lipase_deficiency|LIPA-related_disorder": 1,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease|not_specified": 1,
    "Wolman_disease|LIPA-related_disorder": 2,
    "LIPA-related_disorder|not_specified|not_provided": 1,
    "Wolman_disease|Cholesteryl_ester_storage_disease|Lysosomal_acid_lipase_deficiency|not_provided": 2,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Wolman_disease|LIPA-related_disorder|Lysosomal_acid_lipase_deficiency": 1,
    "not_provided|Wolman_disease|Cholesteryl_ester_storage_disease": 1,
    "Cardiovascular_phenotype|not_provided|LIPA-related_disorder|Wolman_disease|Lysosomal_acid_lipase_deficiency": 1,
    "Lysosomal_acid_lipase_deficiency|Wolman_disease|LIPA-related_disorder": 1,
    "Wolman_disease|Cardiovascular_phenotype|LIPA-related_disorder": 1,
    "not_specified|Lysosomal_acid_lipase_deficiency|Wolman_disease": 1,
    "Wolman_disease|LIPA-related_disorder|not_provided|Lysosomal_acid_lipase_deficiency": 1,
    "Wolman_disease|Lysosomal_acid_lipase_deficiency|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Lysosomal_acid_lipase_deficiency|Wolman_disease": 1,
    "Lysosomal_acid_lipase_deficiency|not_provided": 1,
    "not_provided|not_specified|SLC16A12-related_disorder": 1,
    "Juvenile_cataract-microcornea-renal_glucosuria_syndrome": 39,
    "not_specified|Juvenile_cataract-microcornea-renal_glucosuria_syndrome": 5,
    "SLC16A12-related_disorder": 6,
    "Juvenile_cataract-microcornea-renal_glucosuria_syndrome|not_provided|SLC16A12-related_disorder": 1,
    "Juvenile_cataract-microcornea-renal_glucosuria_syndrome|not_specified": 6,
    "Juvenile_cataract-microcornea-renal_glucosuria_syndrome|not_provided": 3,
    "not_provided|Juvenile_cataract-microcornea-renal_glucosuria_syndrome": 3,
    "Developmental_cataract|Juvenile_cataract-microcornea-renal_glucosuria_syndrome": 1,
    "not_specified|SLC16A12-related_disorder": 1,
    "not_specified|Juvenile_cataract-microcornea-renal_glucosuria_syndrome|not_provided": 1,
    "not_provided|Congenital_ocular_coloboma|Juvenile_cataract-microcornea-renal_glucosuria_syndrome": 1,
    "SLC16A12-related_disorder|not_provided": 1,
    "ANKRD1-related_dilated_cardiomyopathy": 183,
    "Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy": 37,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy": 4,
    "ANKRD1-related_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 24,
    "not_provided|ANKRD1-related_dilated_cardiomyopathy": 5,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 2,
    "ANKRD1-related_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|ANKRD1-related_disorder|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|ANKRD1-related_dilated_cardiomyopathy": 6,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|ANKRD1-related_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Systolic_heart_failure|Cardiovascular_phenotype|not_specified|Congenital_total_pulmonary_venous_return_anomaly|not_provided|ANKRD1-related_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction": 1,
    "not_specified|ANKRD1-related_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "ANKRD1-related_disorder|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|ANKRD1-related_dilated_cardiomyopathy|not_provided": 1,
    "ANKRD1-related_dilated_cardiomyopathy|ANKRD1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy|not_provided": 2,
    "ANKRD1-related_disorder": 4,
    "not_provided|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 4,
    "not_provided|Congenital_total_pulmonary_venous_return_anomaly": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Congenital_total_pulmonary_venous_return_anomaly|ANKRD1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_2": 1,
    "Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 2,
    "Cardiomyopathy|not_specified|not_provided|Primary_dilated_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|not_provided|ANKRD1-related_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|ANKRD1-related_dilated_cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy": 1,
    "ANKRD1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|ANKRD1-related_dilated_cardiomyopathy": 4,
    "ANKRD1-related_dilated_cardiomyopathy|ANKRD1-related_disorder|not_specified": 1,
    "not_specified|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_specified|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|Congenital_total_pulmonary_venous_return_anomaly": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_specified": 4,
    "ANKRD1-related_dilated_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_provided": 3,
    "not_specified|ANKRD1-related_dilated_cardiomyopathy|ANKRD1-related_disorder": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_provided|ANKRD1-related_disorder": 1,
    "Congenital_total_pulmonary_venous_return_anomaly|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|ANKRD1-related_disorder|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_disorder|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_2|Congenital_total_pulmonary_venous_return_anomaly": 1,
    "Cardiomyopathy|not_specified|Congenital_total_pulmonary_venous_return_anomaly|Dilated_Cardiomyopathy|_Dominant|Primary_dilated_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_provided|Congenital_total_pulmonary_venous_return_anomaly|not_specified": 1,
    "Congenital_total_pulmonary_venous_return_anomaly|not_specified": 2,
    "ANKRD1-related_disorder|Hypertrophic_cardiomyopathy_2|ANKRD1-related_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|not_specified": 1,
    "Cardiomyopathy|not_specified|Congenital_total_pulmonary_venous_return_anomaly|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "ANKRD1-related_disorder|not_provided|not_specified|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_provided|not_specified|ANKRD1-related_disorder|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_provided|ANKRD1-related_dilated_cardiomyopathy|not_specified": 1,
    "ANKRD1-related_disorder|not_specified|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Primary_dilated_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|not_specified|ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "ANKRD1-related_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|ANKRD1-related_disorder|not_specified": 1,
    "not_provided|not_specified|ANKRD1-related_dilated_cardiomyopathy|Congenital_total_pulmonary_venous_return_anomaly": 1,
    "Primary_dilated_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_disorder|Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Congenital_total_pulmonary_venous_return_anomaly|not_specified|not_provided|ANKRD1-related_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy|ANKRD1-related_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_total_pulmonary_venous_return_anomaly": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|ANKRD1-related_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "not_specified|ANKRD1-related_dilated_cardiomyopathy|ANKRD1-related_disorder|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|ANKRD1-related_dilated_cardiomyopathy|not_specified": 1,
    "ANKRD1-related_disorder|ANKRD1-related_dilated_cardiomyopathy|not_provided": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "ANKRD1-related_dilated_cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Primary_dilated_cardiomyopathy|Congenital_total_pulmonary_venous_return_anomaly": 1,
    "BTAF1-related_disorder": 2,
    "BTAF1-related_disorder|not_specified": 1,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability": 78,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability": 9,
    "KIF11-related_disorder|not_specified|Decreased_total_neutrophil_count|Decreased_total_lymphocyte_count|not_provided": 1,
    "not_specified|not_provided|KIF11-related_disorder": 1,
    "KIF11-related_disorder": 6,
    "Retinal_dystrophy|not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability": 2,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|not_provided": 9,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Optic_atrophy|Inborn_genetic_diseases|Retinal_dystrophy|not_specified": 1,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Inborn_genetic_diseases": 2,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Syndromic_retinitis_pigmentosa": 1,
    "KIF11-related_disorder|not_provided": 9,
    "KIF11-related_disorder|not_provided|not_specified": 1,
    "not_provided|KIF11-related_disorder": 6,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Microcephaly_with_or_without_chorioretinopathy|_lymphedema_or_intellectual_disability_(MCLID)": 1,
    "Microcephaly|Retinal_dysplasia|Lymphedema": 1,
    "Neurodevelopmental_delay|not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability": 2,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|not_provided": 9,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Exudative_vitreoretinopathy_1": 1,
    "KIF11-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|not_specified|not_provided": 1,
    "KIF11-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|KIF11-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|KIF11-related_disorder|not_specified": 1,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|not_specified": 1,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|KIF11-related_disorder": 1,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Microcephaly_and_chorioretinopathy_1|not_provided": 1,
    "Inborn_genetic_diseases|KIF11-related_disorder|not_provided|not_specified": 1,
    "not_provided|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|KIF11-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Decreased_total_neutrophil_count|Decreased_total_lymphocyte_count": 1,
    "not_specified|Microcephaly_with_or_without_chorioretinopathy|_lymphedema|_or_intellectual_disability|not_provided": 1,
    "CYP26C1-related_disorder|not_provided": 2,
    "Optic_nerve_hypoplasia": 3,
    "CYP26C1-related_disorder": 3,
    "not_specified|Focal_facial_dermal_dysplasia_type_IV|CYP26C1-related_disorder|not_provided|Optic_nerve_hypoplasia": 1,
    "Focal_facial_dermal_dysplasia_type_IV": 2,
    "not_provided|CYP26C1-related_disorder": 1,
    "CYP26A1-related_condition": 1,
    "MYOF-related_disorder": 19,
    "not_specified|MYOF-related_disorder": 3,
    "not_provided|MYOF-related_disorder": 5,
    "MYOF-related_disorder|not_provided": 6,
    "Angioedema|_hereditary|_7": 3,
    "not_specified|Angioedema|_hereditary|_7": 1,
    "Angioedema|_hereditary|_7|not_specified": 1,
    "Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome": 8,
    "not_provided|CEP55-related_disorder": 4,
    "CEP55-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|CEP55-related_disorder|Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome": 1,
    "Inborn_genetic_diseases|Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome|not_provided": 1,
    "not_provided|Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome": 1,
    "CEP55-related_disorder|not_provided": 3,
    "CEP55-related_disorder|Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome": 1,
    "CEP55-related_disorder|not_specified|not_provided": 1,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1": 33,
    "Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome|CEP55-related_disorder|not_provided": 1,
    "Abnormality_of_prenatal_development_or_birth": 1,
    "Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome|not_provided": 1,
    "Multinucleated_neurons-anhydramnios-renal_dysplasia-cerebellar_hypoplasia-hydranencephaly_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_10": 1,
    "Microphthalmia|_isolated|_with_coloboma_10": 1,
    "Retinal_dystrophy|Progressive_retinal_dystrophy_due_to_retinol_transport_defect": 1,
    "Unilateral_microphthalmos|Congenital_ocular_coloboma|Microphthalmia": 1,
    "Bilateral_microphthalmos": 2,
    "Microphthalmia|_isolated|_with_coloboma_10|Progressive_retinal_dystrophy_due_to_retinol_transport_defect|not_provided": 1,
    "Progressive_retinal_dystrophy_due_to_retinol_transport_defect|not_provided": 2,
    "Microphthalmia|_isolated|_with_coloboma_10|Progressive_retinal_dystrophy_due_to_retinol_transport_defect|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_retinal_dystrophy_due_to_retinol_transport_defect": 2,
    "Inborn_genetic_diseases|Microphthalmia|_isolated|_with_coloboma_10": 1,
    "Microphthalmia|_isolated|_with_coloboma_10|Bilateral_microphthalmos": 1,
    "RBP4-related_disorder|not_provided": 1,
    "Retinal_dystrophy|not_provided|Progressive_retinal_dystrophy_due_to_retinol_transport_defect": 1,
    "Microphthalmia|_isolated|_with_coloboma_10|Progressive_retinal_dystrophy_due_to_retinol_transport_defect|not_provided|Retinal_dystrophy": 1,
    "Achromatopsia|Cone_dystrophy_4|not_provided": 5,
    "Achromatopsia|Cone_dystrophy_4": 8,
    "Cone_dystrophy_4": 16,
    "not_provided|Achromatopsia_5|Cone_dystrophy_4": 1,
    "not_provided|Cone_dystrophy_4|Achromatopsia": 9,
    "Inborn_genetic_diseases|not_provided|Cone_dystrophy_4|Achromatopsia": 2,
    "Achromatopsia|not_provided|Cone_dystrophy_4|not_specified": 4,
    "not_provided|PDE6C-related_disorder": 8,
    "Achromatopsia|Cone_dystrophy_4|not_provided|not_specified": 1,
    "Achromatopsia|not_specified|not_provided|Cone_dystrophy_4": 1,
    "Achromatopsia_5|not_provided": 1,
    "Achromatopsia|Cone_dystrophy_4|not_specified|not_provided": 2,
    "Achromatopsia|not_provided|Cone_dystrophy_4": 13,
    "Cone_dystrophy_4|Retinal_dystrophy|Achromatopsia": 1,
    "Cone_dystrophy_4|not_provided|Achromatopsia": 3,
    "PDE6C-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Achromatopsia|not_provided|Cone_dystrophy_4": 1,
    "PDE6C-related_disorder|not_specified|Achromatopsia|not_provided|Cone_dystrophy_4": 1,
    "not_specified|Achromatopsia|not_provided|Cone_dystrophy_4": 1,
    "Achromatopsia_5": 10,
    "not_provided|PDE6C-related_disorder|Retinal_dystrophy": 1,
    "Achromatopsia|Inborn_genetic_diseases|Cone_dystrophy_4|not_provided": 1,
    "not_provided|Cone_dystrophy_4": 5,
    "Achromatopsia|not_provided|PDE6C-related_disorder|Cone_dystrophy_4": 1,
    "Cone_dystrophy_4|Achromatopsia|not_provided": 8,
    "Retinal_dystrophy|not_provided|Achromatopsia|Cone_dystrophy_4": 1,
    "Cone_dystrophy_4|not_provided|Achromatopsia|not_specified": 1,
    "Achromatopsia_5|Achromatopsia|not_provided": 1,
    "Cone_dystrophy_4|Achromatopsia": 6,
    "not_provided|Achromatopsia|Cone_dystrophy_4": 2,
    "Cone_dystrophy_4|not_provided": 6,
    "not_provided|not_specified|Achromatopsia|Cone_dystrophy_4": 1,
    "not_provided|not_specified|Cone_dystrophy_4|Achromatopsia": 1,
    "not_specified|not_provided|Cone_dystrophy_4|Achromatopsia": 2,
    "Cone_dystrophy_4|Achromatopsia|not_specified|not_provided": 1,
    "PDE6C-related_disorder|Retinal_dystrophy|Cone_dystrophy_4|not_provided": 1,
    "not_provided|Achromatopsia|not_specified|Cone_dystrophy_4": 1,
    "PDE6C-related_disorder|Achromatopsia|not_provided|Cone_dystrophy_4": 1,
    "Achromatopsia|not_provided|Retinal_dystrophy": 1,
    "Cone-Rod_Dystrophy|_Recessive|not_provided|Achromatopsia": 1,
    "PDE6C-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Achromatopsia_5|Retinal_dystrophy|not_provided|Cone_dystrophy_4": 1,
    "not_provided|Cone_dystrophy_4|not_specified|Achromatopsia": 1,
    "not_specified|not_provided|Achromatopsia|Cone_dystrophy_4": 1,
    "Inborn_genetic_diseases|Achromatopsia|Retinal_dystrophy|not_provided|Cone_dystrophy_4": 1,
    "Neurodevelopmental_disorder_with_growth_retardation|_dysmorphic_facies|_and_corpus_callosum_abnormalities": 8,
    "not_provided|Neurodevelopmental_disorder_with_growth_retardation|_dysmorphic_facies|_and_corpus_callosum_abnormalities": 1,
    "Neurodevelopmental_disorder_with_growth_retardation|_dysmorphic_facies|_and_corpus_callosum_abnormalities|See_cases": 1,
    "FRA10AC1-related_condition": 1,
    "Epilepsy|_familial_temporal_lobe|_1|LGI1-related_disorder|Autosomal_dominant_epilepsy_with_auditory_features|not_specified|not_provided": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|not_provided": 24,
    "Autosomal_dominant_epilepsy_with_auditory_features": 269,
    "Inborn_genetic_diseases|Autosomal_dominant_epilepsy_with_auditory_features": 11,
    "not_provided|Autosomal_dominant_epilepsy_with_auditory_features": 16,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_epilepsy_with_auditory_features": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Epilepsy|_familial_temporal_lobe|_1": 6,
    "Epilepsy|_familial_temporal_lobe|_1|Autosomal_dominant_epilepsy_with_auditory_features": 2,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_familial_temporal_lobe|_1|Autosomal_dominant_epilepsy_with_auditory_features": 1,
    "Epilepsy|_familial_temporal_lobe|_1|Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Epilepsy|_familial_temporal_lobe|_1|not_specified|not_provided": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases": 13,
    "Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|Autosomal_dominant_epilepsy_with_auditory_features": 3,
    "not_provided|LGI1-related_disorder|Autosomal_dominant_epilepsy_with_auditory_features": 2,
    "Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases|Autosomal_dominant_epilepsy_with_auditory_features": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|not_provided|LGI1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_epilepsy_with_auditory_features|not_specified|not_provided|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_provided|Autosomal_dominant_epilepsy_with_auditory_features|not_specified": 1,
    "LGI1-related_disorder|Autosomal_dominant_epilepsy_with_auditory_features|not_provided|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_provided|Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases": 2,
    "not_specified|Autosomal_dominant_epilepsy_with_auditory_features|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|not_provided|Inborn_genetic_diseases": 1,
    "Seizure|Bilateral_tonic-clonic_seizure": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|not_specified": 1,
    "Inborn_genetic_diseases|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_epilepsy_with_auditory_features|not_provided": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|not_provided|Epilepsy|_familial_temporal_lobe|_1": 2,
    "LGI1-related_disorder": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases|not_provided|not_specified|Epilepsy|_familial_temporal_lobe|_1": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_epilepsy_with_auditory_features": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_epilepsy_with_auditory_features": 2,
    "Autosomal_dominant_epilepsy_with_auditory_features|not_specified|not_provided": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Epilepsy|_familial_temporal_lobe|_1|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases|Epilepsy|_familial_temporal_lobe|_1": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_epilepsy_with_auditory_features|not_specified|Epilepsy|_familial_temporal_lobe|_1": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Epilepsy|_familial_temporal_lobe|_1|Autosomal_dominant_epilepsy_with_auditory_features": 2,
    "Autosomal_dominant_epilepsy|Epilepsy|_familial_temporal_lobe|_1": 1,
    "Autosomal_dominant_epilepsy_with_auditory_features|Epilepsy|_familial_temporal_lobe|_1|Seizure": 1,
    "Genitopatellar_syndrome|Epilepsy|_familial_temporal_lobe|_1": 1,
    "Nephrotic_syndrome|_type_3": 279,
    "Nephrotic_syndrome|_type_3|not_provided": 43,
    "not_provided|Nephrotic_syndrome|_type_3": 27,
    "Nephrotic_syndrome|_type_3|Inborn_genetic_diseases": 37,
    "Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|_type_3|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Nephrotic_syndrome|_type_3": 6,
    "PLCE1-related_disorder": 19,
    "Nephrotic_syndrome|_type_3|PLCE1-related_disorder": 2,
    "not_provided|PLCE1-related_disorder|Nephrotic_syndrome|_type_3|Focal_segmental_glomerulosclerosis": 1,
    "PLCE1-related_disorder|not_provided": 9,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_3": 12,
    "Glomerulonephritis": 1,
    "not_provided|not_specified|Nephrotic_syndrome|_type_3": 3,
    "Kidney_disorder|Nephrotic_syndrome|_type_3": 1,
    "PLCE1-related_disorder|Inborn_genetic_diseases|not_provided|Nephrotic_syndrome|_type_3": 1,
    "not_provided|Nephrotic_syndrome|_type_3|not_specified": 2,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_3|not_provided": 2,
    "Nephrotic_syndrome|_type_3|PLCE1-related_disorder|not_provided": 5,
    "not_provided|PLCE1-related_disorder": 6,
    "Nephrotic_syndrome|_type_3|not_provided|not_specified": 2,
    "Nephrotic_syndrome|_type_3|Focal_segmental_glomerulosclerosis|not_provided|not_specified": 1,
    "not_provided|Polycystic_kidney_disease|PLCE1-related_disorder|Nephrotic_syndrome|_type_3": 1,
    "not_specified|Focal_segmental_glomerulosclerosis|not_provided|Nephrotic_syndrome|_type_3": 1,
    "not_specified|not_provided|Kidney_disorder|Nephrotic_syndrome|_type_3": 1,
    "PLCE1-related_disorder|not_provided|Nephrotic_syndrome|_type_3|not_specified": 1,
    "not_specified|Kidney_disorder|Nephrotic_syndrome|_type_3|not_provided": 1,
    "not_provided|Nephrotic_syndrome|_type_3|PLCE1-related_disorder": 2,
    "Kidney_disorder|not_provided|Nephrotic_syndrome|_type_3": 1,
    "Nephrotic_syndrome|_type_3|Kidney_disorder|not_provided": 2,
    "not_specified|Nephrotic_syndrome|_type_3|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|_type_3|PLCE1-related_disorder": 1,
    "not_specified|not_provided|Nephrotic_syndrome|_type_3|Focal_segmental_glomerulosclerosis": 2,
    "Proteinuria|PLCE1-related_disorder|Nephrotic_syndrome|_type_3|not_provided": 1,
    "Nephrotic_syndrome|_type_3|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Nephrotic_syndrome|_type_3": 4,
    "PLCE1-related_disorder|Kidney_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Nephrotic_syndrome|_type_3": 1,
    "Focal_segmental_glomerulosclerosis|Proteinuria|Kidney_disorder|PLCE1-related_disorder|Nephrotic_syndrome|_type_3|not_provided": 1,
    "Nephrotic_syndrome|_type_3|not_specified|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "not_provided|Nephrotic_syndrome|_type_3|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "Kidney_disorder|Nephrotic_syndrome|_type_3|not_provided": 1,
    "not_provided|Nephrotic_syndrome|_type_3|Inborn_genetic_diseases": 2,
    "Nephrotic_syndrome|_type_3|Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|not_provided": 1,
    "Nephrotic_syndrome|_type_3|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Kidney_disorder|Nephrotic_syndrome|_type_3": 1,
    "Nephrotic_syndrome|_type_3|not_specified|not_provided": 2,
    "Focal_segmental_glomerulosclerosis|not_provided|Nephrotic_syndrome|_type_3|not_specified": 1,
    "PLCE1-related_disorder|Nephrotic_syndrome|_type_3|not_provided": 2,
    "Nephrotic_syndrome|_type_3|not_provided|PLCE1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Nephrotic_syndrome|_type_3": 1,
    "Focal_segmental_glomerulosclerosis|Nephrotic_syndrome|_type_3": 1,
    "Nephrotic_syndrome|_type_3|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4": 4,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4|not_provided": 4,
    "HELLS-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4|not_provided": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4": 6,
    "not_provided|HELLS-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4": 1,
    "HELLS-related_disorder|not_provided": 3,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4|HELLS-related_disorder|not_provided": 1,
    "not_provided|HELLS-related_disorder": 2,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4|Inborn_genetic_diseases": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "HELLS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_4": 1,
    "warfarin_response_-_Dosage": 2,
    "CYP2C19:_uncertain_function": 9,
    "not_provided|Clopidogrel_response|CYP2C19:_increased_function": 1,
    "not_provided|Mephenytoin|_poor_metabolism_of|CYP2C19:_no_function": 2,
    "CYP2C19:_normal_function|not_provided": 2,
    "CYP2C19:_decreased_function": 5,
    "CYP2C19:_no_function": 4,
    "not_provided|CYP2C19:_no_function": 1,
    "not_provided|CYP2C19:_decreased_function": 1,
    "Acute_coronary_syndrome|not_provided|Clopidogrel_response|Proguanil|_poor_metabolism_of|Mephenytoin|_poor_metabolism_of|CYP2C19:_no_function": 1,
    "not_provided|not_specified|Clopidogrel_response|Proguanil|_poor_metabolism_of|Mephenytoin|_poor_metabolism_of": 1,
    "Acute_coronary_syndrome": 1,
    "CYP2C19:_normal_function": 2,
    "Warfarin_response": 12,
    "not_specified|not_provided|Warfarin_response|Phenytoin_response|Lesinurad_response|Flurbiprofen_response|Piroxicam_response": 1,
    "Flurbiprofen_response|Piroxicam_response|Lesinurad_response|not_provided": 2,
    "not_specified|not_provided|Lesinurad_response|Flurbiprofen_response|Piroxicam_response": 1,
    "not_provided|Warfarin_response|Glipizide_response|Tolbutamide_response|Phenytoin_response|Flurbiprofen_response|Piroxicam_response|Lesinurad_response": 1,
    "not_provided|Piroxicam_response|Lesinurad_response|Flurbiprofen_response": 1,
    "CYP2C8-related_disorder|Pulmonary_disease|_chronic_obstructive|_susceptibility_to": 1,
    "CYP2C8-related_disorder": 5,
    "CYP2C8_POLYMORPHISM|not_provided": 1,
    "CYP2C8-related_disorder|CYP2C8_POLYMORPHISM|not_provided": 1,
    "CYP2C8-related_disorder|not_provided": 1,
    "DRUG_METABOLISM|_ALTERED|_CYP2C8-RELATED": 1,
    "SORBS1-associated_Hirschsprung_disease": 1,
    "Cutis_Laxa|_Recessive": 18,
    "ALDH18A1-related_de_Barsy_syndrome": 22,
    "ALDH18A1-related_de_Barsy_syndrome|not_provided": 6,
    "not_provided|ALDH18A1-related_de_Barsy_syndrome": 4,
    "Hereditary_spastic_paraplegia|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 74,
    "Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome": 70,
    "ALDH18A1-related_disorder|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|not_specified|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 77,
    "ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|ALDH18A1-related_de_Barsy_syndrome": 1,
    "ALDH18A1-related_disorder|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "Autosomal_recessive_complex_spastic_paraplegia_type_9B": 6,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 10,
    "ALDH18A1-related_de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Abnormality_of_the_nervous_system": 1,
    "not_provided|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 11,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 93,
    "Inborn_genetic_diseases|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|ALDH18A1-related_disorder": 2,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_disorder": 2,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided|ALDH18A1-related_de_Barsy_syndrome": 2,
    "not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 13,
    "not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|ALDH18A1-related_disorder": 2,
    "ALDH18A1-related_de_Barsy_syndrome|not_provided|ALDH18A1-related_disorder|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Hereditary_spastic_paraplegia": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|Hereditary_spastic_paraplegia_5A": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1-related_disorder|not_specified|Hereditary_spastic_paraplegia|ALDH18A1-related_de_Barsy_syndrome|not_provided": 1,
    "not_provided|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A": 3,
    "not_specified|not_provided|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Hereditary_spastic_paraplegia_9A|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|not_provided": 2,
    "not_provided|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_complex_spastic_paraplegia_type_9B|not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Spondyloepiphyseal_dysplasia|_Stanescu_type": 1,
    "de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|not_provided": 2,
    "not_provided|ALDH18A1-related_de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "Cutis_laxa|_autosomal_dominant_3": 4,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Hereditary_ataxia|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Inborn_genetic_diseases": 1,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1-related_de_Barsy_syndrome": 6,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome": 4,
    "not_provided|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9": 5,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9": 8,
    "not_specified|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|ALDH18A1-related_disorder": 1,
    "not_provided|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3": 15,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|not_specified": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided|ALDH18A1-related_disorder": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Intellectual_disability": 1,
    "Hereditary_spastic_paraplegia_9A": 6,
    "Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|not_provided": 2,
    "ALDH18A1-related_disorder|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "ALDH18A1-related_de_Barsy_syndrome|Hereditary_spastic_paraplegia_9A|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 1,
    "ALDH18A1-related_disorder": 10,
    "not_provided|Intellectual_disability|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|ALDH18A1-related_de_Barsy_syndrome|Hereditary_spastic_paraplegia_9A": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1_deficiency": 1,
    "Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A": 1,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Hereditary_spastic_paraplegia_9A|Autosomal_recessive_complex_spastic_paraplegia_type_9B|ALDH18A1-related_de_Barsy_syndrome": 1,
    "not_specified|Hereditary_spastic_paraplegia|ALDH18A1-related_de_Barsy_syndrome|not_provided|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "not_provided|ALDH18A1-related_disorder|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3": 1,
    "ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 4,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|not_provided|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|not_provided": 6,
    "not_provided|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "ALDH18A1_deficiency": 1,
    "not_provided|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|Inborn_genetic_diseases": 1,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|not_provided": 6,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|not_specified": 2,
    "not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|ALDH18A1-related_de_Barsy_syndrome": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome": 1,
    "Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|not_specified|ALDH18A1-related_de_Barsy_syndrome": 1,
    "P5CS_deficiency": 1,
    "ALDH18A1-related_de_Barsy_syndrome|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Hereditary_spastic_paraplegia_9A|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|not_provided|ALDH18A1-related_de_Barsy_syndrome": 1,
    "not_specified|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 2,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_9A": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_specified|ALDH18A1-related_de_Barsy_syndrome|not_provided": 1,
    "P5CS_deficiency|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Hereditary_spastic_paraplegia": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Hereditary_spastic_paraplegia": 3,
    "Hereditary_spastic_paraplegia|Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|not_provided|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "ALDH18A1-related_de_Barsy_syndrome|not_provided|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "ALDH18A1-related_disorder|ALDH18A1-related_de_Barsy_syndrome|not_provided|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3": 1,
    "Hereditary_spastic_paraplegia|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided|ALDH18A1-related_disorder|ALDH18A1-related_de_Barsy_syndrome": 1,
    "de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|not_provided|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_specified|not_provided|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "not_specified|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 1,
    "not_provided|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Inborn_genetic_diseases": 1,
    "ALDH18A1-related_de_Barsy_syndrome|not_provided|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "Hereditary_spastic_paraplegia_9A|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 3,
    "not_provided|Hereditary_spastic_paraplegia|Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|not_specified|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|ALDH18A1-related_disorder|Autosomal_recessive_complex_spastic_paraplegia_type_9B|ALDH18A1-related_de_Barsy_syndrome|Hereditary_spastic_paraplegia_9A": 1,
    "Hereditary_spastic_paraplegia|Autosomal_recessive_complex_spastic_paraplegia_type_9B": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1-related_disorder": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 3,
    "not_provided|Hereditary_spastic_paraplegia|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_de_Barsy_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|not_provided": 1,
    "ALDH18A1-related_disorder|not_provided|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 2,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|not_provided|ALDH18A1-related_de_Barsy_syndrome|Inborn_genetic_diseases|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Spondyloepiphyseal_dysplasia|_Stanescu_type": 1,
    "not_provided|Inborn_genetic_diseases|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|not_provided|Hereditary_spastic_paraplegia|ALDH18A1-related_de_Barsy_syndrome|ALDH18A1-related_disorder": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_de_Barsy_syndrome|Hereditary_spastic_paraplegia_9A|Autosomal_recessive_complex_spastic_paraplegia_type_9B": 1,
    "not_provided|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|not_provided|Hereditary_spastic_paraplegia": 1,
    "ALDH18A1-related_disorder|not_provided|Hereditary_spastic_paraplegia_9A": 1,
    "ALDH18A1-related_disorder|not_provided|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Inborn_genetic_diseases": 2,
    "ALDH18A1-related_de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|ALDH18A1_deficiency|Hereditary_spastic_paraplegia_9A|not_provided": 1,
    "Autosomal_recessive_complex_spastic_paraplegia_type_9B|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|not_provided": 1,
    "ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "P5CS_deficiency|Hereditary_spastic_paraplegia_9A": 1,
    "not_provided|ALDH18A1-related_disorder|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Hereditary_spastic_paraplegia|not_provided|ALDH18A1-related_disorder|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Inborn_genetic_diseases": 1,
    "Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|Cutis_Laxa|_Recessive": 1,
    "Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Hereditary_spastic_paraplegia_9A|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_disorder|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant_3|not_provided|Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B": 1,
    "Autosomal_recessive_complex_spastic_paraplegia_type_9B|not_provided|ALDH18A1-related_disorder|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|Hereditary_spastic_paraplegia_9A": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Hereditary_spastic_paraplegia_9A": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|not_provided|Hereditary_spastic_paraplegia": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|ALDH18A1-related_de_Barsy_syndrome|not_provided": 1,
    "P5CS_deficiency|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "not_specified|not_provided|ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A": 1,
    "ALDH18A1-related_disorder|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|not_provided|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "not_provided|Hereditary_spastic_paraplegia|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|Inborn_genetic_diseases|Hearing_impairment|Intellectual_disability": 1,
    "Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3|not_provided|not_specified|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Cutis_laxa|_autosomal_dominant_3": 1,
    "not_provided|ALDH18A1-related_de_Barsy_syndrome|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A|Cutis_laxa|_autosomal_dominant_3": 1,
    "not_provided|ALDH18A1-related_disorder|ALDH18A1-related_de_Barsy_syndrome|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3": 1,
    "ALDH18A1-related_de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A|Inborn_genetic_diseases": 1,
    "Intellectual_disability|Cutis_laxa|_autosomal_dominant_3|Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome": 1,
    "Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|Cutis_laxa|_autosomal_dominant_3|de_Barsy_syndrome|not_provided|Autosomal_recessive_complex_spastic_paraplegia_type_9B|Hereditary_spastic_paraplegia_9A|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Autosomal_dominant_spastic_paraplegia_type_9|de_Barsy_syndrome|Cutis_laxa|_autosomal_dominant_3|not_provided|ALDH18A1-related_disorder": 1,
    "ALDH18A1-related_de_Barsy_syndrome|ALDH18A1-related_disorder|not_provided": 1,
    "not_specified|ALDH18A1-related_de_Barsy_syndrome|ALDH18A1-related_disorder": 1,
    "Cutis_Laxa|_Recessive|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_provided|ALDH18A1-related_de_Barsy_syndrome": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 190,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 160,
    "not_provided|Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_18|not_provided|Orofacial-digital_syndrome_IV": 1,
    "Inborn_genetic_diseases|Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 17,
    "TCTN3-related_disorder|not_provided|Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 2,
    "Orofacial-digital_syndrome_IV": 6,
    "not_provided|Orofacial-digital_syndrome_IV|Joubert_syndrome_18|Inborn_genetic_diseases": 2,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 7,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 2,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_specified": 3,
    "not_provided|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 6,
    "not_specified|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|Inborn_genetic_diseases": 5,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TCTN3-related_disorder|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_18": 6,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|not_specified": 4,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|not_provided": 5,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_provided": 7,
    "Inborn_genetic_diseases|Joubert_syndrome_18|Orofacial-digital_syndrome_IV|TCTN3-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_specified|Inborn_genetic_diseases": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_specified|not_provided": 5,
    "TCTN3-related_disorder|Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|TCTN3-related_disorder": 2,
    "TCTN3-related_disorder|not_specified|Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_provided": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|Joubert_syndrome_and_related_disorders": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_provided|not_specified": 3,
    "not_specified|Joubert_syndrome_18|Orofacial-digital_syndrome_IV|See_cases|not_provided": 1,
    "TCTN3-related_disorder|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "TCTN3-related_disorder|not_provided|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "not_specified|not_provided|Orofacial-digital_syndrome_IV|Joubert_syndrome_18": 2,
    "Inborn_genetic_diseases|Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_provided": 1,
    "TCTN3-related_disorder": 2,
    "Joubert_syndrome_18|Orofacial-digital_syndrome_IV|Joubert_syndrome_and_related_disorders|TCTN3-related_disorder": 1,
    "Joubert_syndrome_and_related_disorders|Orofacial-digital_syndrome_IV|Joubert_syndrome_18|not_provided": 1,
    "Orofacial-digital_syndrome_IV|Joubert_syndrome_18|Ciliopathy": 1,
    "Joubert_syndrome_and_related_disorders|not_provided|Joubert_syndrome_18|Orofacial-digital_syndrome_IV": 1,
    "Joubert_syndrome_and_related_disorders|Orofacial-digital_syndrome_IV|Joubert_syndrome_18|TCTN3-related_disorder": 1,
    "not_provided|Hereditary_spastic_paraplegia_64": 8,
    "Hereditary_spastic_paraplegia_64|not_provided": 2,
    "Hereditary_spastic_paraplegia_64": 117,
    "Hereditary_spastic_paraplegia_64|Inborn_genetic_diseases": 10,
    "Hereditary_spastic_paraplegia_64|ENTPD1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_64|Hereditary_spastic_paraplegia|Global_developmental_delay|Microcephaly|Polymicrogyria|not_provided": 1,
    "Hereditary_spastic_paraplegia_64|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_64|not_provided|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_64|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_64": 3,
    "ENTPD1-related_disorder": 2,
    "Hereditary_spastic_paraplegia_64|Hereditary_spastic_paraplegia": 3,
    "Hereditary_spastic_paraplegia_64|not_provided|Hereditary_spastic_paraplegia": 2,
    "ENTPD1-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_64": 1,
    "Hereditary_spastic_paraplegia_64|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 2,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_64": 1,
    "Hereditary_spastic_paraplegia_64|Hereditary_spastic_paraplegia|not_provided": 1,
    "ENTPD1-related_disorder|Hereditary_spastic_paraplegia_64|not_provided|Hereditary_spastic_paraplegia": 1,
    "Agammaglobulinemia_4|_autosomal_recessive": 263,
    "Inborn_genetic_diseases|Agammaglobulinemia_4|_autosomal_recessive": 11,
    "Agammaglobulinemia_4|_autosomal_recessive|Inborn_genetic_diseases": 12,
    "Agammaglobulinemia_4|_autosomal_recessive|not_specified": 3,
    "Agammaglobulinemia_4|_autosomal_recessive|not_provided": 4,
    "not_provided|Agammaglobulinemia_4|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Agammaglobulinemia_4|_autosomal_recessive": 9,
    "Agammaglobulinemia_4|_autosomal_recessive|BLNK-related_disorder": 1,
    "BLNK-related_disorder|not_provided|Agammaglobulinemia_4|_autosomal_recessive": 1,
    "BLNK-related_disorder|not_specified|not_provided|Agammaglobulinemia_4|_autosomal_recessive": 1,
    "BLNK-related_disorder": 2,
    "not_provided|not_specified|Agammaglobulinemia_4|_autosomal_recessive": 1,
    "BLNK-related_disorder|Agammaglobulinemia_4|_autosomal_recessive": 3,
    "not_specified|Agammaglobulinemia_4|_autosomal_recessive|not_provided": 2,
    "Agammaglobulinemia_4|_autosomal_recessive|not_provided|not_specified": 1,
    "Proximal_muscle_weakness|Tongue_fasciculations|EMG:_neuropathic_changes|Hand_tremor|Proximal_amyotrophy|Spinal_muscular_atrophy|Muscular_atrophy": 2,
    "not_specified|Infantile_spasms": 25,
    "Infantile_spasms|not_specified": 17,
    "not_provided|not_specified|Infantile_spasms": 2,
    "PIK3AP1-related_disorder|Infantile_spasms": 7,
    "Infantile_spasms|not_provided": 3,
    "not_provided|Infantile_spasms": 12,
    "PIK3AP1-related_early_onset_epileptic_encephalopathy": 1,
    "PIK3AP1-related_disorder|Infantile_spasms|not_provided": 1,
    "PIK3AP1-related_disorder": 1,
    "Infantile_spasms|not_specified|not_provided": 1,
    "Infantile_spasms|PIK3AP1-related_disorder": 2,
    "not_provided|Infantile_spasms|PIK3AP1-related_disorder": 2,
    "PIK3AP1-Associated_Seizure_Disorder": 1,
    "not_specified|not_provided|Infantile_spasms": 1,
    "Pontocerebellar_hypoplasia|_type_1F": 1,
    "Intellectual_disability|Neurodevelopmental_abnormality": 1,
    "Primary_hyperoxaluria_type_3|not_provided": 59,
    "Primary_hyperoxaluria_type_3": 155,
    "Primary_hyperoxaluria_type_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Primary_hyperoxaluria_type_3": 50,
    "Primary_hyperoxaluria_type_3|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Primary_hyperoxaluria_type_3": 2,
    "HOGA1-related_disorder|not_provided|Primary_hyperoxaluria_type_3": 4,
    "Primary_hyperoxaluria_type_3|not_provided|HOGA1-related_disorder": 1,
    "Primary_hyperoxaluria_type_3|not_specified": 3,
    "not_provided|Primary_hyperoxaluria_type_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_hyperoxaluria_type_3": 4,
    "not_provided|Inborn_genetic_diseases|Primary_hyperoxaluria_type_3": 1,
    "Primary_hyperoxaluria_type_3|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|HOGA1-related_disorder": 1,
    "Primary_hyperoxaluria_type_3|not_provided|not_specified": 1,
    "Primary_hyperoxaluria_type_3|not_specified|not_provided": 1,
    "Primary_hyperoxaluria_type_3|not_specified|not_provided|HOGA1-related_disorder": 1,
    "Inborn_genetic_diseases|Primary_hyperoxaluria_type_3|not_provided": 1,
    "not_provided|Primary_hyperoxaluria_type_3|not_specified": 1,
    "not_specified|Primary_hyperoxaluria_type_3": 1,
    "Primary_hyperoxaluria|not_provided": 1,
    "Neurodevelopmental_disorder_with_hyperkinetic_movements|_seizures|_and_structural_brain_abnormalities": 2,
    "Hereditary_spastic_paraplegia_33": 44,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_33": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_33|not_provided": 3,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_33|Spastic_paraplegia": 2,
    "Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia_33": 1,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_33": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_33|not_specified|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_33": 1,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia_33|not_provided": 1,
    "Hereditary_spastic_paraplegia_33|Spastic_paraplegia": 4,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_33": 2,
    "ZFYVE27-related_disorder|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_33|not_specified|Spastic_tetraparesis|not_provided|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_33|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_33|not_specified": 2,
    "not_specified|Hereditary_spastic_paraplegia_33|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_33|not_provided": 8,
    "not_provided|Hereditary_spastic_paraplegia_33": 3,
    "GOLGA7B-related_condition": 1,
    "Pyridine_Nucleotide-Disulfide_Oxidoreductase_Domain_2_related_mitochanodrial_defect": 1,
    "Hermansky-Pudlak_syndrome_1": 137,
    "not_provided|Hermansky-Pudlak_syndrome_1": 66,
    "Hermansky-Pudlak_syndrome_1|not_provided": 40,
    "Hermansky-Pudlak_syndrome_1|not_specified|not_provided": 6,
    "not_provided|Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome": 7,
    "Hermansky-Pudlak_syndrome|HPS1-related_disorder|not_provided|Hermansky-Pudlak_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|HPS1-related_disorder|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|not_specified|not_provided": 2,
    "not_provided|HPS1-related_disorder": 3,
    "Hermansky-Pudlak_syndrome|not_provided|Hermansky-Pudlak_syndrome_1": 2,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_1": 6,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|not_provided": 5,
    "Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome": 3,
    "Hermansky-Pudlak_syndrome_1|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|HPS1-related_disorder|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_1": 1,
    "HPS1-related_disorder|not_provided": 2,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_1": 4,
    "not_provided|HPS1-related_disorder|Hermansky-Pudlak_syndrome_1": 2,
    "Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome|not_provided": 2,
    "Hermansky-Pudlak_syndrome|not_specified|not_provided|Hermansky-Pudlak_syndrome_1|HPS1-related_disorder": 1,
    "not_provided|Hermansky-Pudlak_syndrome_1|HPS1-related_disorder": 1,
    "HPS1-related_disorder|not_specified|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 1,
    "Hermansky-Pudlak_syndrome_1|not_provided|Hermansky-Pudlak_syndrome": 7,
    "not_provided|HPS1-related_disorder|Hermansky-Pudlak_syndrome_1|not_specified": 1,
    "Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome|HPS1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 17,
    "not_provided|Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome|HPS1-related_disorder": 1,
    "Hermansky-Pudlak_syndrome_1|not_specified|not_provided|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 2,
    "Hermansky-Pudlak_syndrome_1|not_provided|Hermansky-Pudlak_syndrome|Inborn_genetic_diseases": 1,
    "HPS1-related_disorder|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 4,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_1": 2,
    "Hermansky-Pudlak_syndrome|not_specified|Hermansky-Pudlak_syndrome_1": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 2,
    "Hermansky-Pudlak_syndrome_1|not_provided|Hermansky-Pudlak_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_1": 5,
    "Hermansky-Pudlak_syndrome_1|not_provided|not_specified": 2,
    "HPS1-related_disorder|not_provided|Hermansky-Pudlak_syndrome": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome": 2,
    "HPS1-related_disorder|not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 1,
    "Hermansky-Pudlak_syndrome_1|not_specified|Hermansky-Pudlak_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 1,
    "HPS1-related_disorder|Hermansky-Pudlak_syndrome|not_provided": 2,
    "not_specified|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|not_provided": 3,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|not_specified|not_provided|HPS1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Hermansky-Pudlak_syndrome_1|not_provided|Hermansky-Pudlak_syndrome": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|not_specified": 1,
    "not_provided|HPS1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_with_pulmonary_fibrosis|not_provided": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome": 1,
    "not_provided|Hermansky-Pudlak_syndrome_1|not_specified": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|not_provided": 1,
    "Hermansky-Pudlak_syndrome_1|Inborn_genetic_diseases": 4,
    "Hermansky-Pudlak_syndrome|HPS1-related_disorder|Hermansky-Pudlak_syndrome_1|not_provided": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1|Inborn_genetic_diseases": 1,
    "HPS1-related_disorder": 2,
    "Hermansky-Pudlak_syndrome|HPS1-related_disorder": 1,
    "HPS1-related_disorder|not_provided|Hermansky-Pudlak_syndrome_1": 1,
    "not_provided|Hermansky-Pudlak_syndrome_1|not_specified|Hermansky-Pudlak_syndrome": 2,
    "Hermansky-Pudlak_syndrome|HPS1-related_disorder|not_provided": 2,
    "HPS1-related_disorder|Hermansky-Pudlak_syndrome_1|Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome": 1,
    "not_provided|Hermansky-Pudlak_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome_1": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_1|HPS1-related_disorder|Hermansky-Pudlak_syndrome": 1,
    "not_specified|HPS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|HPS1-related_disorder|not_specified|Hermansky-Pudlak_syndrome_1": 1,
    "HPS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_1|not_provided|not_specified": 1,
    "Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_1": 1,
    "Hermansky-Pudlak_syndrome_1|Hermansky-Pudlak_syndrome|not_provided|HPS1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_1|HPS1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Hermansky-Pudlak_syndrome_1": 1,
    "Urofacial_syndrome_type_1|not_provided": 7,
    "Urofacial_syndrome_type_1": 62,
    "Urofacial_syndrome_type_1|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|not_provided|Urofacial_syndrome_type_1": 1,
    "not_provided|Urofacial_syndrome_type_1": 7,
    "HPSE2-related_disorder": 4,
    "Inborn_genetic_diseases|Urofacial_syndrome_type_1": 5,
    "Urofacial_syndrome_type_1|Ochoa_syndrome|not_provided": 1,
    "Urofacial_syndrome_type_1|HPSE2-related_disorder|not_provided": 1,
    "HPSE2-related_disorder|not_provided": 2,
    "not_provided|Urofacial_syndrome_type_1|Inborn_genetic_diseases": 2,
    "Urofacial_syndrome_type_1|HPSE2-related_disorder|Inborn_genetic_diseases": 1,
    "Urofacial_syndrome_type_1|not_provided|HPSE2-related_disorder": 1,
    "not_provided|Urofacial_syndrome_type_1|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Urofacial_syndrome_type_1|Ochoa_syndrome": 1,
    "Ochoa_syndrome": 1,
    "not_provided|Urofacial_syndrome_type_1|HPSE2-related_disorder": 1,
    "HPSE2-related_disorder|Urofacial_syndrome_type_1": 1,
    "ASPARTATE_AMINOTRANSFERASE|_SERUM_LEVEL_OF|_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "GOT1-related_disorder": 3,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|not_specified": 1,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2": 6,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|not_provided|not_specified": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2": 7,
    "Inborn_genetic_diseases|not_specified|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2": 1,
    "not_provided|Leigh_syndrome|not_specified": 2,
    "COX15-related_disorder|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|Leigh_syndrome|not_provided": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|Inborn_genetic_diseases": 1,
    "not_provided|COX15-related_disorder": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|not_provided": 3,
    "Leigh_syndrome|not_provided|COX15-related_disorder": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|not_provided|Inborn_genetic_diseases": 1,
    "Leigh_syndrome|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2": 2,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|COX15-related_disorder|Leigh_syndrome|not_specified": 1,
    "COX15-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2": 1,
    "COX15-related_disorder|not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|Leigh_syndrome|See_cases": 1,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|Leigh_syndrome": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|not_provided|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_2|not_provided|Leigh_syndrome": 1,
    "COX15-related_disorder": 1,
    "Dubin-Johnson_syndrome": 63,
    "not_provided|ABCC2-related_disorder|not_specified|Dubin-Johnson_syndrome": 1,
    "ABCC2-related_disorder": 33,
    "ABCC2-related_disorder|Dubin-Johnson_syndrome|not_provided": 6,
    "not_provided|Dubin-Johnson_syndrome": 37,
    "Dubin-Johnson_syndrome|not_provided": 42,
    "Dubin-Johnson_syndrome|not_provided|ABCC2-related_disorder": 9,
    "not_provided|ABCC2-related_disorder": 29,
    "ABCC2-related_disorder|not_provided|Dubin-Johnson_syndrome": 13,
    "not_specified|not_provided|Dubin-Johnson_syndrome": 4,
    "Dubin-Johnson_syndrome|Inborn_genetic_diseases": 4,
    "ABCC2-related_disorder|not_provided": 37,
    "Inborn_genetic_diseases|ABCC2-related_disorder": 4,
    "ABCC2-related_disorder|Dubin-Johnson_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Dubin-Johnson_syndrome|ABCC2-related_disorder|not_provided": 6,
    "ABCC2-related_disorder|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|ABCC2-related_disorder": 1,
    "ABCC2-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|ABCC2-related_disorder|Dubin-Johnson_syndrome": 7,
    "Dubin-Johnson_syndrome|ABCC2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Dubin-Johnson_syndrome|ABCC2-related_disorder": 3,
    "ABCC2-related_disorder|not_specified|not_provided|Dubin-Johnson_syndrome": 6,
    "Inborn_genetic_diseases|Dubin-Johnson_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|ABCC2-related_disorder|not_provided": 1,
    "Dubin-Johnson_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Dubin-Johnson_syndrome|not_provided|ABCC2-related_disorder": 1,
    "ABCC2-related_disorder|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "ABCC2-related_disorder|not_provided|Inborn_genetic_diseases|Dubin-Johnson_syndrome": 1,
    "ABCC2-related_disorder|Dubin-Johnson_syndrome": 1,
    "not_specified|Dubin-Johnson_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|ABCC2-related_disorder": 1,
    "ABCC2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Dubin-Johnson_syndrome": 2,
    "Dubin-Johnson_syndrome|not_provided|not_specified|ABCC2-related_disorder": 1,
    "not_specified|ABCC2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Dubin-Johnson_syndrome|ABCC2-related_disorder": 1,
    "Dubin-Johnson_syndrome|ABCC2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Dubin-Johnson_syndrome": 1,
    "not_specified|Dubin-Johnson_syndrome|not_provided": 1,
    "DNMBP-related_disorder": 38,
    "not_provided|DNMBP-related_disorder|Cataract_48": 4,
    "Cataract_48|DNMBP-related_disorder|not_provided": 2,
    "Cataract_48": 5,
    "not_specified|DNMBP-related_disorder": 1,
    "DNMBP-related_disorder|not_provided": 1,
    "not_provided|DNMBP-related_disorder": 1,
    "CPN1-related_disorder": 3,
    "Anaphylotoxin_inactivator_deficiency": 2,
    "not_specified|Anaphylotoxin_inactivator_deficiency|not_provided|CPN1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_62": 79,
    "Hereditary_spastic_paraplegia_62|not_provided": 4,
    "not_provided|Hereditary_spastic_paraplegia_62": 3,
    "Hereditary_spastic_paraplegia_62|not_specified": 6,
    "Hereditary_spastic_paraplegia_62|Hereditary_spastic_paraplegia": 3,
    "not_specified|Hereditary_spastic_paraplegia_62": 3,
    "Hereditary_spastic_paraplegia_62|not_provided|ERLIN1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_62|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_62": 1,
    "ERLIN1-related_disorder": 1,
    "CHUK-related_disorder|not_provided": 2,
    "not_provided|CHUK-related_disorder": 3,
    "Cocoon_syndrome": 2,
    "Bartsocas-Papas_syndrome_2": 1,
    "CWF19L1-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_17": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_17|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_17": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_17": 21,
    "CWF19L1-related_disorder|not_provided": 2,
    "CWF19L1-related_disorder": 7,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_17": 2,
    "not_specified|CWF19L1-related_disorder|not_provided": 2,
    "not_provided|CWF19L1-related_disorder": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_32": 7,
    "NDUFB8-related_disorder|not_provided": 3,
    "NDUFB8-related_disorder": 3,
    "not_provided|NDUFB8-related_disorder": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_32|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_32|not_provided": 1,
    "PAX2-related_disorder": 17,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|not_specified|not_provided": 2,
    "Focal_segmental_glomerulosclerosis_7": 35,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 167,
    "Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 92,
    "PAX2-related_disorder|Focal_segmental_glomerulosclerosis_7": 1,
    "not_provided|not_specified|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 1,
    "not_specified|Renal_coloboma_syndrome|not_provided|Focal_segmental_glomerulosclerosis_7": 1,
    "Renal_coloboma_syndrome": 38,
    "Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|not_specified": 2,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|not_provided": 5,
    "PAX2-related_disorder|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Glomerular_sclerosis": 1,
    "PAX2-related_disorder|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 4,
    "PAX2-related_disorder|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 2,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|Inborn_genetic_diseases": 5,
    "not_provided|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 6,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|PAX2-related_disorder": 5,
    "Congenital_anomalies_of_kidney_and_urinary_tract_1|Focal_segmental_glomerulosclerosis_7": 1,
    "Papillorenal_syndrome_with_macular_abnormalities": 1,
    "not_specified|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 1,
    "Renal_coloboma_syndrome|PAX2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|not_provided": 10,
    "Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|PAX2-related_disorder": 6,
    "not_provided|Renal_coloboma_syndrome": 2,
    "Renal_coloboma_syndrome|PAX2-related_disorder|Focal_segmental_glomerulosclerosis_7|not_provided|See_cases": 1,
    "Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome": 1,
    "Steroid-resistant_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Renal_coloboma_syndrome": 1,
    "not_provided|PAX2-related_disorder|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 7,
    "Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 1,
    "PAX2-related_disorder|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|not_provided|not_specified|Retinal_dystrophy": 1,
    "Renal_cysts_and_diabetes_syndrome": 188,
    "not_provided|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|Inborn_genetic_diseases": 1,
    "Renal_hypoplasia": 1,
    "PAX2-related_disorder|Inborn_genetic_diseases|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 1,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7": 1,
    "Renal_coloboma_syndrome|not_provided": 1,
    "Renal_coloboma_syndrome|Focal_segmental_glomerulosclerosis_7|Retinal_dystrophy": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|PAX2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome|not_specified|PAX2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 1,
    "not_provided|Retinal_dystrophy|PAX2-related_disorder|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_7|Renal_coloboma_syndrome": 1,
    "Atelis_syndrome_1": 5,
    "SLF2-related_disorder": 2,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia": 6,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia": 1,
    "Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided|Autosomal_recessive_cerebellar_ataxia|not_specified": 1,
    "Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Perrault_syndrome_5|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Autosomal_recessive_cerebellar_ataxia": 1,
    "Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 3,
    "Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 5,
    "Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia": 1,
    "Mitochondrial_DNA_depletion_syndrome|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Ataxia_Neuropathy_Spectrum_Disorders|not_provided|Autosomal_recessive_cerebellar_ataxia": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Infantile_onset_spinocerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia": 3,
    "Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Mitochondrial_DNA_depletion_syndrome|Ataxia_Neuropathy_Spectrum_Disorders|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Autosomal_recessive_cerebellar_ataxia": 1,
    "TWNK-related_disorder": 7,
    "Perrault_syndrome_5": 2,
    "Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "not_provided|TWNK-related_disorder": 7,
    "Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|not_provided": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia": 2,
    "not_provided|Perrault_syndrome_5": 1,
    "Autosomal_recessive_cerebellar_ataxia|not_provided|Hereditary_spastic_paraplegia|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 2,
    "Infantile_onset_spinocerebellar_ataxia|not_provided": 3,
    "Perrault_syndrome_5|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia": 1,
    "Mitochondrial_DNA_depletion_syndrome|Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Ataxia_Neuropathy_Spectrum_Disorders": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 16,
    "Perrault_syndrome_5|Hereditary_spastic_paraplegia": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|not_provided|Infantile_onset_spinocerebellar_ataxia": 1,
    "TWNK-related_disorder|not_provided": 6,
    "mitochondrial_hepatopathy": 3,
    "Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|Perrault_syndrome_5": 1,
    "Autosomal_recessive_cerebellar_ataxia|not_specified|not_provided|Hereditary_spastic_paraplegia|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided": 3,
    "TWNK-related_disorder|not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Perrault_syndrome_5|not_provided": 1,
    "not_provided|Mitochondrial_disease|TWNK-related_disorder|Perrault_syndrome_5|Infantile_onset_spinocerebellar_ataxia|Perrault_syndrome": 1,
    "not_provided|Infantile_onset_spinocerebellar_ataxia": 5,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Perrault_syndrome_5": 1,
    "not_specified|not_provided|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 6,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Autosomal_recessive_cerebellar_ataxia|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 2,
    "See_cases|Infantile_onset_spinocerebellar_ataxia": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Perrault_syndrome|not_provided": 1,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_digenic|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "not_provided|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Autosomal_recessive_cerebellar_ataxia|Hereditary_spastic_paraplegia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "not_specified|Infantile_onset_spinocerebellar_ataxia|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|Hereditary_spastic_paraplegia": 1,
    "Progressive_external_ophthalmoplegia|Neuromuscular_dysphagia|EMG:_myopathic_abnormalities|Depression|Bilateral_sensorineural_hearing_impairment|Bilateral_ptosis|Dysphonia|Abnormal_mitochondria_in_muscle_tissue|not_provided|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Mitochondrial_disease": 1,
    "Perrault_syndrome|Autosomal_recessive_cerebellar_ataxia|Perrault_syndrome_5|not_provided|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Perrault_syndrome_5|Infantile_onset_spinocerebellar_ataxia": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Perrault_syndrome|Infantile_onset_spinocerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia": 1,
    "not_specified|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|not_provided|Autosomal_recessive_cerebellar_ataxia": 1,
    "not_provided|mitochondrial_hepatopathy": 1,
    "not_provided|Perrault_syndrome|Perrault_syndrome_5": 1,
    "not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Perrault_syndrome_5": 1,
    "TWNK-related_disorder|not_provided|Infantile_onset_spinocerebellar_ataxia": 1,
    "Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Infantile_onset_spinocerebellar_ataxia|Perrault_syndrome_5|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|Perrault_syndrome_5|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 3,
    "TWNK-related_disorder|Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Perrault_syndrome|Perrault_syndrome_5|not_specified|not_provided": 1,
    "Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided": 1,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Autosomal_recessive_cerebellar_ataxia|not_specified": 1,
    "Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided|Autosomal_recessive_cerebellar_ataxia": 1,
    "Perrault_syndrome_5|Infantile_onset_spinocerebellar_ataxia|not_provided|Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|TWNK-related_disorder|not_provided|Hereditary_spastic_paraplegia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_specified": 1,
    "not_provided|Perrault_syndrome_5|Infantile_onset_spinocerebellar_ataxia": 1,
    "Autosomal_recessive_cerebellar_ataxia|not_provided|Infantile_onset_spinocerebellar_ataxia|TWNK-related_disorder|not_specified|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "TWNK-related_disorder|not_specified|not_provided": 1,
    "TWNK-related_disorder|not_provided|not_specified": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Autosomal_recessive_cerebellar_ataxia|not_specified|not_provided": 1,
    "Perrault_syndrome|Perrault_syndrome_5|not_provided": 1,
    "Perrault_syndrome|not_specified|not_provided": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Perrault_syndrome_5|Infantile_onset_spinocerebellar_ataxia": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|TWNK-related_disorder": 1,
    "Autosomal_recessive_cerebellar_ataxia|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 2,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_provided|Infantile_onset_spinocerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia": 1,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|TWNK-related_disorder|Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|not_specified": 1,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "not_provided|Infantile_onset_spinocerebellar_ataxia|Perrault_syndrome_5|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "Autosomal_recessive_cerebellar_ataxia|Perrault_syndrome_5|Infantile_onset_spinocerebellar_ataxia|not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 1,
    "TWNK-related_disorder|Autosomal_recessive_cerebellar_ataxia|Hereditary_spastic_paraplegia|not_provided|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Ataxia_Neuropathy_Spectrum_Disorders|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Mitochondrial_DNA_depletion_syndrome|Autosomal_recessive_cerebellar_ataxia|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Infantile_onset_spinocerebellar_ataxia": 1,
    "Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Hereditary_spastic_paraplegia|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia": 1,
    "Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Infantile_onset_spinocerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 2,
    "Infantile_onset_spinocerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Mitochondrial_DNA_depletion_syndrome|Ataxia_Neuropathy_Spectrum_Disorders|Autosomal_recessive_cerebellar_ataxia": 1,
    "Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "Autosomal_recessive_cerebellar_ataxia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Infantile_onset_spinocerebellar_ataxia": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Autosomal_recessive_cerebellar_ataxia|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_3|Infantile_onset_spinocerebellar_ataxia": 1,
    "Mitochondrial_DNA_depletion_syndrome|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|Ataxia_Neuropathy_Spectrum_Disorders|Autosomal_recessive_cerebellar_ataxia": 1,
    "Hearing_loss|_autosomal_recessive_57|not_provided": 3,
    "not_provided|PDZD7-related_disorder": 7,
    "not_provided|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C": 1,
    "PDZD7-related_disorder|Hearing_loss|_autosomal_recessive_57|not_specified|not_provided|Hearing_impairment": 1,
    "not_specified|not_provided|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C": 2,
    "not_provided|Hearing_loss|_autosomal_recessive_57|Usher_syndrome|_type_IIC|_GPR98/PDZD7_digenic": 2,
    "not_provided|PDZD7-related_disorder|not_specified": 2,
    "Hearing_loss|_autosomal_recessive_57": 16,
    "not_specified|Hearing_loss|_autosomal_recessive_57|not_provided|Usher_syndrome_type_2C": 2,
    "not_specified|not_provided|Hearing_loss|_autosomal_recessive_57": 1,
    "not_provided|Usher_syndrome_type_2C|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57": 1,
    "PDZD7-related_disorder|not_specified|not_provided": 3,
    "PDZD7-related_disorder": 3,
    "PDZD7-related_disorder|not_provided|not_specified": 1,
    "Nonsyndromic_genetic_hearing_loss|Hearing_loss|_autosomal_recessive": 1,
    "PDZD7-related_disorder|not_provided|Usher_syndrome_type_2C|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57|Usher_syndrome|_type_IIC|_GPR98/PDZD7_digenic|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_recessive_57|not_provided": 1,
    "Retinal_dystrophy|Hearing_loss|_autosomal_recessive_57": 1,
    "not_provided|Usher_syndrome_type_2C|Hearing_loss|_autosomal_recessive_57": 1,
    "not_provided|Hearing_loss|_autosomal_recessive_57": 3,
    "not_provided|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C": 2,
    "Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C|not_specified|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_57|not_provided|not_specified": 1,
    "PDZD7-related_disorder|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_provided|Usher_syndrome_type_2A|Usher_syndrome_type_2C|Hearing_loss|_autosomal_recessive_57|not_specified": 1,
    "PDZD7-related_disorder|not_provided": 2,
    "Usher_syndrome_type_2C|not_specified|Hearing_loss|_autosomal_recessive_57|not_provided": 1,
    "Usher_syndrome_type_2C|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2A|not_provided": 1,
    "Retinal_dystrophy|not_provided|Hearing_impairment": 1,
    "not_provided|PDZD7-related_disorder|Hearing_loss|_autosomal_recessive_57": 1,
    "not_provided|PDZD7-related_disorder|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2C|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C": 1,
    "not_provided|not_specified|Usher_syndrome_type_2A|Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C|PDZD7-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|PDZD7-related_disorder": 1,
    "Usher_syndrome_type_2C|not_provided|Hearing_loss|_autosomal_recessive_57": 1,
    "Hearing_loss|_autosomal_recessive_57|Usher_syndrome_type_2C|Usher_syndrome_type_2A|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2C|Hearing_loss|_autosomal_recessive_57|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_2A|not_provided": 1,
    "not_provided|not_specified|PDZD7-related_disorder": 1,
    "BTRC-related_disorder": 2,
    "not_provided|BTRC-related_disorder": 5,
    "BTRC-related_disorder|not_provided": 2,
    "POLL-related_disorder": 2,
    "Split_hand-foot_malformation_3": 22,
    "Ectrodactyly": 3,
    "not_provided|Split_hand-foot_malformation_3": 6,
    "Split_hand-foot_malformation_3|not_specified": 3,
    "Split_hand-foot_malformation_3|not_provided": 3,
    "not_provided|Split_hand-foot_malformation_3|not_specified": 2,
    "not_specified|Split_hand-foot_malformation_3|not_provided": 2,
    "FBXW4-related_disorder": 1,
    "not_provided|FBXW4-related_disorder": 2,
    "FBXW4-related_disorder|not_specified": 1,
    "FBXW4-related_disorder|Split_hand-foot_malformation_3|not_specified|not_provided": 1,
    "Split_hand-foot_malformation_3|not_specified|not_provided": 1,
    "Ectrodactyly|not_provided": 2,
    "FBXW4-related_disorder|not_provided": 1,
    "Holoprosencephaly_1|not_provided|Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 1,
    "not_specified|FGF8-related_disorder|not_provided": 1,
    "Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 12,
    "See_cases|Holoprosencephaly_sequence": 1,
    "FGF8-related_disorder": 4,
    "Hypogonadotropic_hypogonadism_6_with_or_without_anosmia|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_6_with_or_without_anosmia|not_provided": 1,
    "Holoprosencephaly_sequence|not_provided|Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 1,
    "not_provided|Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 1,
    "Semilobar_holoprosencephaly|not_provided|Holoprosencephaly_sequence|Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 1,
    "Semilobar_holoprosencephaly": 1,
    "Hypogonadotropic_hypogonadism_6_with_or_without_anosmia|FGF8-related_disorder": 1,
    "not_provided|FGF8-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 1,
    "Holoprosencephaly_sequence|Peters_plus_syndrome|not_provided": 1,
    "Hypogonadotropic_hypogonadism_6_with_or_without_anosmia|FGF8-related_disorder|Holoprosencephaly_sequence|not_provided": 1,
    "not_provided|FGF8-related_disorder": 2,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_6_with_or_without_anosmia": 1,
    "not_provided|HPS6-related_disorder|not_specified|Hermansky-Pudlak_syndrome_6": 1,
    "not_provided|Hermansky-Pudlak_syndrome_6": 19,
    "Hermansky-Pudlak_syndrome_6": 34,
    "Hermansky-Pudlak_syndrome_6|not_provided": 17,
    "not_provided|HPS6-related_disorder": 3,
    "not_provided|Hermansky-Pudlak_syndrome|HPS6-related_disorder": 2,
    "not_specified|Hermansky-Pudlak_syndrome_6|not_provided": 1,
    "HPS6-related_disorder|Hermansky-Pudlak_syndrome_6|not_specified|not_provided": 1,
    "not_provided|HPS6-related_disorder|not_specified": 1,
    "Hermansky-Pudlak_syndrome_6|Hermansky-Pudlak_syndrome|not_provided": 2,
    "HPS6-related_disorder": 3,
    "Hermansky-Pudlak_syndrome|not_provided|Hermansky-Pudlak_syndrome_6": 1,
    "not_provided|Hermansky-Pudlak_syndrome_6|not_specified": 2,
    "Hermansky-Pudlak_syndrome_6|HPS6-related_disorder|not_specified|not_provided": 1,
    "not_specified|Hermansky-Pudlak_syndrome_6|not_provided|HPS6-related_disorder": 1,
    "Hermansky-Pudlak_syndrome_6|not_specified|not_provided": 2,
    "not_provided|not_specified|HPS6-related_disorder|Hermansky-Pudlak_syndrome_6": 1,
    "HPS6-related_disorder|not_provided": 5,
    "not_specified|not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_6": 1,
    "not_provided|not_specified|HPS6-related_disorder": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_6": 6,
    "not_provided|Hermansky-Pudlak_syndrome_6|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome_6|HPS6-related_disorder|Storage_pool_disease_of_platelets|not_provided": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome_6": 2,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_6": 3,
    "Hermansky-Pudlak_syndrome_6|Hermansky-Pudlak_syndrome": 1,
    "not_specified|Hermansky-Pudlak_syndrome_6": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_6|HPS6-related_disorder": 1,
    "HPS6-related_disorder|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_6|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_6": 1,
    "not_provided|Hermansky-Pudlak_syndrome_6|HPS6-related_disorder": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_6|not_provided": 1,
    "not_provided|Hermansky-Pudlak_syndrome_6|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_6|Inborn_genetic_diseases|not_provided": 1,
    "Hermansky-Pudlak_syndrome_6|not_specified|not_provided|HPS6-related_disorder": 1,
    "Hermansky-Pudlak_syndrome_6|not_provided|not_specified": 1,
    "PPRC1-related_disorder": 22,
    "not_provided|PPRC1-related_disorder": 5,
    "PPRC1-related_conditon": 1,
    "PPRC1-related_conditon|not_specified": 1,
    "PITX3-related_disorder|not_provided": 1,
    "PITX3-related_disorder": 5,
    "not_specified|Inborn_genetic_diseases|PITX3-related_disorder|not_provided": 1,
    "Cataract_11_multiple_types|not_provided": 1,
    "Cataract_11_multiple_types|ANTERIOR_SEGMENT_DYSGENESIS_1|_MULTIPLE_SUBTYPES|PITX3-related_disorder|Cataract_11|_posterior_polar|not_provided": 1,
    "Anterior_segment_dysgenesis_1|Cataract_11_multiple_types|not_provided": 1,
    "Cataract_11|_posterior_polar|Cataract_11|_posterior_polar|_with_microphthalmia_and_neurodevelopmental_abnormalities": 1,
    "Anterior_segment_dysgenesis_1|Cataract_11_multiple_types|not_provided|not_specified": 1,
    "Anterior_segment_dysgenesis_1": 1,
    "not_provided|Cataract_11_multiple_types": 1,
    "Charcot-Marie-Tooth_Disease|_axonal|_type_2GG": 13,
    "Charcot-Marie-Tooth_Disease|_axonal|_type_2GG|Charcot-Marie-Tooth_disease|_dominant_intermediate_A": 1,
    "not_specified|Charcot-Marie-Tooth_Disease|_axonal|_type_2GG": 1,
    "not_provided|GBF1-related_disorder": 1,
    "Charcot-Marie-Tooth_Disease|_axonal|_type_2GG|not_provided": 1,
    "Charcot-Marie-Tooth_Disease|_axonal|_type_2GG|not_specified": 1,
    "Charcot-Marie-Tooth_Disease|_axonal|_type_2GG|Motor_axonal_neuropathy": 4,
    "GBF1-related_disorder": 1,
    "NFKB2-related_disorder": 6,
    "Immunodeficiency|_common_variable|_10": 591,
    "NFKB2-related_disorder|Immunodeficiency|_common_variable|_10": 15,
    "Immunodeficiency|_common_variable|_10|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_10": 18,
    "not_provided|Immunodeficiency|_common_variable|_10": 9,
    "Immunodeficiency|_common_variable|_10|not_provided": 25,
    "Immunodeficiency|_common_variable|_10|NFKB2-related_disorder": 7,
    "Immunodeficiency|_common_variable|_10|not_specified": 4,
    "not_provided|Immunodeficiency|_common_variable|_10|NFKB2-related_disorder": 1,
    "Immunodeficiency|_common_variable|_10|not_specified|not_provided": 3,
    "NFKB2-related_disorder|not_provided": 1,
    "Immunodeficiency|_common_variable|_10|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Immunodeficiency|_common_variable|_10": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_10|NFKB2-related_disorder": 1,
    "Immunodeficiency|_common_variable|_10|NFKB2-related_disorder|not_provided": 1,
    "not_specified|Immunodeficiency|_common_variable|_10|NFKB2-related_disorder|not_provided": 1,
    "NFKB2-related_disorder|Immunodeficiency|_common_variable|_10|Inborn_genetic_diseases": 1,
    "Immunodeficiency|_common_variable|_10|not_specified|Inborn_genetic_diseases": 1,
    "NFKB2-related_disorder|Immunodeficiency|_common_variable|_10|not_provided": 1,
    "Immunodeficiency|_common_variable|_10|not_provided|not_specified": 1,
    "Immunodeficiency|_common_variable|_10|not_provided|NFKB2-related_disorder": 1,
    "Immunodeficiency|_common_variable|_10|Immunodeficiency|_common_variable|_1": 1,
    "Immunodeficiency|_common_variable|_10|not_specified|NFKB2-related_disorder": 1,
    "not_specified|not_provided|NFKB2-related_disorder|Immunodeficiency|_common_variable|_10": 1,
    "NFKB2-related_disorder|not_provided|Immunodeficiency|_common_variable|_10": 1,
    "NFKB2-related_disorder|Inborn_genetic_diseases|Immunodeficiency|_common_variable|_10": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_10|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_10|not_provided": 1,
    "Immunodeficiency|_common_variable|_10|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Common_variable_immunodeficiency|Inherited_Immunodeficiency_Diseases|Immunodeficiency|_common_variable|_10|not_specified|not_provided": 1,
    "Immunodeficiency|_common_variable|_1|Immunodeficiency|_common_variable|_10": 1,
    "Inborn_genetic_diseases|NFKB2-related_disorder|Immunodeficiency|_common_variable|_10": 1,
    "Gorlin_syndrome|Medulloblastoma": 315,
    "Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma": 110,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|not_specified": 1,
    "not_provided|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Familial_meningioma|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 5,
    "Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 169,
    "Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome": 72,
    "not_provided|Familial_meningioma|Basal_cell_nevus_syndrome_2|Medulloblastoma|Joubert_syndrome_32|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 72,
    "Familial_meningioma|Joubert_syndrome_32|Medulloblastoma|Basal_cell_nevus_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Medulloblastoma|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|not_provided": 1,
    "Basal_cell_nevus_syndrome_2|Medulloblastoma|Familial_meningioma|Joubert_syndrome_32|Gorlin_syndrome|not_provided": 1,
    "Gorlin_syndrome|Basal_cell_nevus_syndrome_2|Medulloblastoma|Familial_meningioma|Joubert_syndrome_32|not_provided": 1,
    "Familial_meningioma|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Gorlin_syndrome|Medulloblastoma|Familial_meningioma": 2,
    "Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Joubert_syndrome_32|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Medulloblastoma": 8,
    "Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "SUFU-related_disorder|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 11,
    "Gorlin_syndrome|Medulloblastoma|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 131,
    "not_provided|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome|not_provided": 2,
    "Basal_cell_nevus_syndrome_2|Medulloblastoma|Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|not_provided": 10,
    "Familial_meningioma|Gorlin_syndrome|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome|Familial_meningioma": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 171,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Gorlin_syndrome|Medulloblastoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|Familial_meningioma|not_provided": 1,
    "Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Familial_meningioma|not_provided": 1,
    "Joubert_syndrome_32": 4,
    "not_provided|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Gorlin_syndrome|Medulloblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Basal_cell_nevus_syndrome_1|not_provided|Medulloblastoma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Familial_meningioma|Gorlin_syndrome": 1,
    "SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Familial_meningioma|Joubert_syndrome_32|Gorlin_syndrome|Medulloblastoma|not_provided": 1,
    "Gorlin_syndrome|Medulloblastoma|not_provided|SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Medulloblastoma|Gorlin_syndrome|not_provided": 3,
    "Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Familial_meningioma|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 1,
    "not_provided|Medulloblastoma|Gorlin_syndrome": 2,
    "Medulloblastoma|Gorlin_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|SUFU-related_disorder|Gorlin_syndrome|Joubert_syndrome_32|Medulloblastoma|not_provided": 1,
    "Basal_cell_nevus_syndrome_2|Medulloblastoma|Familial_meningioma|Joubert_syndrome_32|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "SUFU-related_disorder": 2,
    "not_specified|Gorlin_syndrome|Medulloblastoma|not_provided|SUFU-related_disorder": 1,
    "SUFU-related_disorder|Gorlin_syndrome|Medulloblastoma": 2,
    "Joubert_syndrome_32|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|See_cases": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|SUFU-related_disorder|Medulloblastoma|Gorlin_syndrome|not_specified|not_provided": 1,
    "not_provided|Gorlin_syndrome|Medulloblastoma": 4,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|SUFU-related_disorder|not_provided": 1,
    "Oculomotor_apraxia": 1,
    "Medulloblastoma|Gorlin_syndrome|SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Medulloblastoma|not_provided|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Medulloblastoma|not_specified|not_provided|Familial_meningioma|Joubert_syndrome_32|Basal_cell_nevus_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Oculomotor_apraxia_-_Cogan_type": 1,
    "Gorlin_syndrome|Medulloblastoma|Joubert_syndrome_32|Familial_meningioma|Basal_cell_nevus_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|Familial_meningioma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32": 1,
    "Gorlin_syndrome|Medulloblastoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_meningioma": 1,
    "Medulloblastoma|Familial_meningioma|Joubert_syndrome_32|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Medulloblastoma|Gorlin_syndrome": 3,
    "not_provided|Gorlin_syndrome|Medulloblastoma|SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Gorlin_syndrome|Medulloblastoma": 2,
    "not_specified|Medulloblastoma|Gorlin_syndrome": 1,
    "SUFU-related_ocular_motor_apraxia": 1,
    "Familial_meningioma|Joubert_syndrome_32|Basal_cell_nevus_syndrome_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Joubert_syndrome_32|Medulloblastoma|Gorlin_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Gorlin_syndrome|Medulloblastoma": 1,
    "Joubert_syndrome_32|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma": 4,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|Familial_meningioma": 2,
    "not_provided|Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|SUFU-related_disorder|Craniopharyngioma": 1,
    "Gorlin_syndrome|Medulloblastoma|Congenital_fibrosarcoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome|Familial_meningioma": 1,
    "Gorlin_syndrome|Medulloblastoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|not_provided": 1,
    "not_provided|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome|Medulloblastoma": 1,
    "Gorlin_syndrome|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Medulloblastoma|SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Gorlin_syndrome|Medulloblastoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Basal_cell_nevus_syndrome_1|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma": 1,
    "SUFU-related_disorder|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 3,
    "SUFU-related_disorder|Medulloblastoma|Gorlin_syndrome|not_specified|not_provided|Meningioma": 1,
    "Gorlin_syndrome|Medulloblastoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 1,
    "Gorlin_syndrome|Medulloblastoma|Familial_meningioma|Joubert_syndrome_32|Basal_cell_nevus_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|SUFU-related_disorder|Gorlin_syndrome|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma|not_provided|Familial_meningioma": 1,
    "Basal_cell_nevus_syndrome_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Medulloblastoma|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Medulloblastoma|not_provided": 5,
    "Gorlin_syndrome|Medulloblastoma|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 1,
    "Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Medulloblastoma|Familial_meningioma|Joubert_syndrome_32": 1,
    "Familial_meningioma|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_meningioma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gorlin_syndrome|Medulloblastoma|not_specified|Microform_holoprosencephaly": 1,
    "Basal_cell_nevus_syndrome_2|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|SUFU-related_disorder": 1,
    "Joubert_syndrome_32|Basal_cell_nevus_syndrome_2|Gorlin_syndrome|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|not_provided|Gorlin_syndrome|Medulloblastoma|SUFU-related_disorder|Joubert_syndrome_32|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|SUFU-related_disorder|not_provided|Medulloblastoma|Gorlin_syndrome": 1,
    "not_provided|Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_specified|Joubert_syndrome_32": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Gorlin_syndrome|Medulloblastoma": 1,
    "Familial_meningioma|Gorlin_syndrome|Joubert_syndrome_32|Hereditary_cancer-predisposing_syndrome|not_provided|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma": 14,
    "not_specified|Gorlin_syndrome|Medulloblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_meningioma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Familial_meningioma|Gorlin_syndrome|Joubert_syndrome_32": 1,
    "Familial_meningioma|Medulloblastoma|Basal_cell_nevus_syndrome_2|Joubert_syndrome_32|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome|Medulloblastoma": 3,
    "Hereditary_cancer-predisposing_syndrome|Joubert_syndrome_32|Medulloblastoma|Basal_cell_nevus_syndrome_2|Familial_meningioma|Gorlin_syndrome": 1,
    "Gorlin_syndrome|Medulloblastoma|not_specified": 1,
    "Basal_cell_nevus_syndrome_1|Gorlin_syndrome|Medulloblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Medulloblastoma|Familial_meningioma|not_specified": 1,
    "Gorlin_syndrome|Medulloblastoma|Joubert_syndrome_32": 1,
    "Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Joubert_syndrome_32|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "SUFU-related_disorder|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Gorlin_syndrome|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma": 1,
    "Medulloblastoma|Joubert_syndrome_32|Basal_cell_nevus_syndrome_2|Familial_meningioma|not_specified|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Joubert_syndrome_32|Medulloblastoma|Gorlin_syndrome": 1,
    "Familial_meningioma|not_provided|Medulloblastoma|Gorlin_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gorlin_syndrome|Medulloblastoma|not_specified|SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|B_Lymphoblastic_Leukemia/Lymphoma|_Not_Otherwise_Specified|Familial_meningioma|Gorlin_syndrome|Medulloblastoma": 1,
    "not_provided|Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Joubert_syndrome_32|not_specified": 1,
    "Familial_meningioma|Joubert_syndrome_32|Basal_cell_nevus_syndrome_2|Medulloblastoma|Gorlin_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Gorlin_syndrome|Medulloblastoma|Joubert_syndrome_32|not_provided": 1,
    "Basal_cell_nevus_syndrome_2|Medulloblastoma|Familial_meningioma|Joubert_syndrome_32|Hereditary_cancer-predisposing_syndrome|Gorlin_syndrome": 1,
    "SUFU-related_disorder|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Gorlin_syndrome|not_provided": 1,
    "not_provided|SUFU-related_disorder": 1,
    "not_provided|not_specified|Joubert_syndrome_32|Gorlin_syndrome": 1,
    "TRIM8-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome": 14,
    "TRIM8-related_disorder|not_provided": 7,
    "Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome|not_provided": 1,
    "TRIM8-related_disorder": 2,
    "not_provided|TRIM8-related_disorder": 2,
    "Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome|Seizure|Focal_segmental_glomerulosclerosis|Neurodevelopmental_delay": 3,
    "Inborn_genetic_diseases|not_provided|TRIM8-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis|Seizure|Neurodevelopmental_delay|Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome|not_provided": 1,
    "Neurodevelopmental_delay|Focal_segmental_glomerulosclerosis|Seizure|Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome": 1,
    "Neurodevelopmental_delay|Focal_segmental_glomerulosclerosis|Seizure|not_provided": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome": 1,
    "Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome|Inborn_genetic_diseases|not_provided|Seizure|Neurodevelopmental_delay|Focal_segmental_glomerulosclerosis|TRIM8-related_epileptic_encephalopathy": 1,
    "Focal_segmental_glomerulosclerosis_and_neurodevelopmental_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|Seizure|Neurodevelopmental_delay": 1,
    "not_provided|Joubert_syndrome_35|Retinitis_pigmentosa_83": 1,
    "Joubert_syndrome_35|not_provided": 2,
    "not_provided|Joubert_syndrome_35": 1,
    "ARL3-related_disorder|not_provided": 1,
    "Progressive_cone_degeneration|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_83": 2,
    "Joubert_syndrome_35": 1,
    "Retinitis_pigmentosa_83": 2,
    "ARL3-related_disorder": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase": 64,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase": 27,
    "Deficiency_of_steroid_17-alpha-monooxygenase|not_provided": 39,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|not_provided|Deficiency_of_steroid_17-alpha-monooxygenase": 2,
    "Deficiency_of_steroid_17-alpha-monooxygenase|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|not_provided|Congenital_adrenal_hyperplasia": 1,
    "not_provided|CYP17A1-related_disorder": 2,
    "Inborn_genetic_diseases|Deficiency_of_steroid_17-alpha-monooxygenase": 2,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial": 4,
    "not_provided|Congenital_adrenal_hyperplasia|Deficiency_of_steroid_17-alpha-monooxygenase": 2,
    "Congenital_adrenal_hyperplasia|Deficiency_of_steroid_17-alpha-monooxygenase|not_provided": 1,
    "Congenital_adrenal_hyperplasia|not_provided|Deficiency_of_steroid_17-alpha-monooxygenase": 1,
    "not_provided|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|Deficiency_of_steroid_17-alpha-monooxygenase|CYP17A1-related_disorder": 1,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|Deficiency_of_steroid_17-alpha-monooxygenase": 1,
    "not_provided|CYP17A1-related_disorder|Deficiency_of_steroid_17-alpha-monooxygenase": 1,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|Deficiency_of_steroid_17-alpha-monooxygenase|not_provided": 2,
    "Congenital_adrenal_hyperplasia|Deficiency_of_steroid_17-alpha-monooxygenase": 2,
    "Deficiency_of_steroid_17-alpha-monooxygenase|not_specified|not_provided": 1,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase|CYP17A1-related_disorder": 1,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase|Congenital_adrenal_hyperplasia": 2,
    "Deficiency_of_steroid_17-alpha-monooxygenase|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|CYP17A1-related_disorder|not_provided|Congenital_adrenal_hyperplasia": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|not_provided|17|20-lyase_deficiency|_isolated|Congenital_adrenal_hyperplasia": 1,
    "17|20-lyase_deficiency|_isolated|Deficiency_of_steroid_17-alpha-monooxygenase|not_provided": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|not_provided|Congenital_adrenal_hyperplasia": 1,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial": 1,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase|Inborn_genetic_diseases": 1,
    "Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|Deficiency_of_steroid_17-alpha-monooxygenase": 1,
    "CYP17A1-related_disorder|not_provided|Deficiency_of_steroid_17-alpha-monooxygenase": 2,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete": 6,
    "CYP17A1-related_disorder|not_provided": 1,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial|Breast_cancer|_susceptibility_to": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|CYP17A1-related_disorder|not_provided": 1,
    "not_provided|Congenital_adrenal_hyperplasia|Deficiency_of_steroid_17-alpha-monooxygenase|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete": 1,
    "CYP17A1-related_disorder|Deficiency_of_steroid_17-alpha-monooxygenase|not_provided": 1,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial|Deficiency_of_steroid_17-alpha-monooxygenase|not_specified": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|Congenital_adrenal_hyperplasia": 1,
    "not_provided|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|CYP17A1-related_disorder|Deficiency_of_steroid_17-alpha-monooxygenase": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|not_provided|Congenital_adrenal_hyperplasia|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|not_provided|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|Congenital_adrenal_hyperplasia": 1,
    "not_provided|17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial": 1,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_partial|Deficiency_of_steroid_17-alpha-monooxygenase|not_provided": 1,
    "not_provided|Deficiency_of_steroid_17-alpha-monooxygenase|Congenital_adrenal_hyperplasia|CYP17A1-related_disorder": 1,
    "17-alpha-hydroxylase/17|20-lyase_deficiency|_combined_complete|not_provided": 1,
    "Deficiency_of_steroid_17-alpha-monooxygenase|Congenital_adrenal_hyperplasia|not_provided": 1,
    "Renal_hypomagnesemia_6": 40,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6": 41,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6|not_provided": 4,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Renal_hypomagnesemia_6": 13,
    "CNNM2-related_disorder": 7,
    "not_provided|Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1": 7,
    "not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6": 5,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1": 24,
    "Inborn_genetic_diseases|Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6|not_provided": 2,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6|Inborn_genetic_diseases": 1,
    "not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1": 2,
    "CNNM2-related_disorder|not_provided|Renal_hypomagnesemia_6": 1,
    "Renal_hypomagnesemia_6|CNNM2-related_disorder|Hypomagnesemia|_seizures|_and_intellectual_disability_1|not_provided": 1,
    "Renal_hypomagnesemia_6|not_provided": 5,
    "Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1|not_provided": 8,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|not_provided": 2,
    "Renal_hypomagnesemia_6|not_provided|CNNM2-related_disorder": 1,
    "Hypomagnesemia": 1,
    "not_provided|CNNM2-related_disorder": 1,
    "not_provided|Renal_hypomagnesemia_6|CNNM2-related_disorder": 1,
    "Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1|See_cases": 1,
    "CNNM2-Related_Disorders": 1,
    "CNNM2-related_neurodevelopmental_disorder_and_hypomagnesemia": 1,
    "not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_1|Inborn_genetic_diseases": 1,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1|Inborn_genetic_diseases": 1,
    "Hypomagnesemia|_seizures|_and_intellectual_disability_1|Renal_hypomagnesemia_6|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypomagnesemia|_seizures|_and_intellectual_disability_1": 1,
    "Inborn_genetic_diseases|not_provided|Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1": 1,
    "Renal_hypomagnesemia_6|Hypomagnesemia|_seizures|_and_intellectual_disability_1|not_provided|Inborn_genetic_diseases": 1,
    "Renal_Hypomagnesemia|_Dominant": 2,
    "Hereditary_spastic_paraplegia_45|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_45": 148,
    "Hereditary_spastic_paraplegia_45|Hereditary_spastic_paraplegia": 3,
    "not_provided|Hereditary_spastic_paraplegia_45": 5,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_45": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_45": 6,
    "NT5C2-related_disorder": 2,
    "Neurodevelopmental_disorder|Hereditary_spastic_paraplegia_45": 1,
    "Hereditary_spastic_paraplegia_45|not_provided": 4,
    "NT5C2-related_disorder|Hereditary_spastic_paraplegia_45": 1,
    "not_specified|Hereditary_spastic_paraplegia_45|not_provided": 1,
    "Hereditary_spastic_paraplegia_45|Inborn_genetic_diseases": 2,
    "NT5C2-related_disorder|Hereditary_spastic_paraplegia_45|not_provided": 1,
    "Microcephaly|Hereditary_spastic_paraplegia_45": 1,
    "Hereditary_spastic_paraplegia_45|not_specified": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_45": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_45": 1,
    "Hereditary_spastic_paraplegia_45|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spastic_paraplegia_45|not_provided|not_specified": 1,
    "Mitochondrial_complex_5_(ATP_synthase)_deficiency|_nuclear_type_6": 3,
    "not_provided|Mitochondrial_complex_5_(ATP_synthase)_deficiency|_nuclear_type_6": 1,
    "not_provided|Inborn_genetic_diseases|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_2": 2,
    "Brain_disorder|not_provided": 1,
    "STN1-related_disorder|not_provided": 2,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_2|Inborn_genetic_diseases|STN1-related_disorder": 1,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_2": 3,
    "Brain_disorder": 1,
    "STN1-related_disorder": 3,
    "not_provided|STN1-related_disorder": 2,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_2|not_provided": 3,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_2": 2,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_2|Inborn_genetic_diseases|not_provided": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|COL17A1-related_disorder": 1,
    "COL17A1-related_disorder": 5,
    "Epithelial_recurrent_erosion_dystrophy|Epidermolysis_bullosa|_junctional_4|_intermediate": 8,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|COL17A1-related_disorder|not_provided": 2,
    "not_provided|COL17A1-related_disorder|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 4,
    "not_provided|COL17A1-related_disorder": 9,
    "Epidermolysis_bullosa|_junctional_4|_intermediate": 18,
    "Epithelial_recurrent_erosion_dystrophy|Epidermolysis_bullosa|_junctional_4|_intermediate|not_provided": 2,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy|COL17A1-related_disorder|not_provided": 2,
    "Epithelial_recurrent_erosion_dystrophy": 5,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|not_specified|Epithelial_recurrent_erosion_dystrophy": 5,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy": 1,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|not_provided": 5,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 2,
    "COL17A1-related_disorder|Epithelial_recurrent_erosion_dystrophy|not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate": 1,
    "Junctional_epidermolysis_bullosa|Epithelial_recurrent_erosion_dystrophy|Epidermolysis_bullosa|_junctional_4|_intermediate|not_provided": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 4,
    "Inborn_genetic_diseases|COL17A1-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate": 1,
    "COL17A1-related_disorder|Junctional_epidermolysis_bullosa": 1,
    "COL17A1-related_disorder|Epithelial_recurrent_erosion_dystrophy|Late-onset_junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|not_provided|Junctional_epidermolysis_bullosa": 1,
    "COL17A1-related_disorder|not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate": 1,
    "not_provided|Abnormality_of_the_skin": 1,
    "not_provided|Amelogenesis_imperfecta_type_1A": 1,
    "not_provided|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 2,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy|not_provided": 3,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|COL17A1-related_disorder|Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy|not_provided|Junctional_epidermolysis_bullosa": 1,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy|not_provided|Amelogenesis_imperfecta_type_1A": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified|Epithelial_recurrent_erosion_dystrophy": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 2,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|COL17A1-related_disorder": 3,
    "COL17A1-related_disorder|Junctional_epidermolysis_bullosa|_non-Herlitz_type|High_myopia": 1,
    "not_provided|Epithelial_recurrent_erosion_dystrophy|Epidermolysis_bullosa|_junctional_4|_intermediate": 2,
    "not_provided|Epithelial_recurrent_erosion_dystrophy|Corneal_dystrophy": 1,
    "COL17A1-related_disorder|not_provided": 6,
    "COL17A1-related_disorder|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified|not_provided|Epithelial_recurrent_erosion_dystrophy": 4,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified|Epithelial_recurrent_erosion_dystrophy|not_provided": 1,
    "not_provided|Epithelial_recurrent_erosion_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|COL17A1-related_disorder": 3,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Epidermolysis_bullosa|_junctional_4|_intermediate": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy": 1,
    "Epidermolysis_bullosa|_junctional_4|_intermediate|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "COL17A1-related_disorder|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 2,
    "Junctional_epidermolysis_bullosa|not_provided|Epithelial_recurrent_erosion_dystrophy|Epidermolysis_bullosa|_junctional_4|_intermediate": 1,
    "not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy": 1,
    "not_provided|Epithelial_recurrent_erosion_dystrophy|not_specified|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Epithelial_recurrent_erosion_dystrophy|Amelogenesis_imperfecta_type_1A|not_provided": 1,
    "not_provided|COL17A1-related_disorder|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|Epithelial_recurrent_erosion_dystrophy": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Inborn_genetic_diseases": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Epithelial_recurrent_erosion_dystrophy": 2,
    "not_provided|Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy|COL17A1-related_disorder|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "not_specified|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|COL17A1-related_disorder|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Epithelial_recurrent_erosion_dystrophy|Amelogenesis_imperfecta_type_1A": 1,
    "not_provided|Amelogenesis_imperfecta_type_1A|Inborn_genetic_diseases|COL17A1-related_disorder|Epidermolysis_bullosa|_junctional_4|_intermediate|Epithelial_recurrent_erosion_dystrophy": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified": 1,
    "CFAP43-related_disorder": 20,
    "not_specified|CFAP43-related_disorder": 1,
    "Normal_pressure_hydrocephalus|Spermatogenic_failure_19": 2,
    "Normal_pressure_hydrocephalus": 5,
    "Spermatogenic_failure_19": 14,
    "not_specified|CFAP43-related_disorder|not_provided": 3,
    "Normal_pressure_hydrocephalus|not_specified": 2,
    "not_provided|CFAP43-related_disorder": 1,
    "Spermatogenic_failure_19|not_provided|not_specified": 1,
    "CFAP43-related_disorder|not_specified": 1,
    "CFAP43-related_disorder|not_provided": 1,
    "GSTO1-related_disorder": 2,
    "CFAP58-related_disorder": 1,
    "Spermatogenic_failure_49": 6,
    "CFAP58-related_disorder|not_specified": 1,
    "SORCS3-related_disorder": 4,
    "Alzheimer_disease_6": 1,
    "Cerebral_palsy|_spastic_quadriplegic|_3": 3,
    "Complex_neurodevelopmental_disorder_with_motor_features|not_specified": 2,
    "Cerebral_palsy|_spastic_quadriplegic|_3|not_provided": 1,
    "not_provided|Cerebral_palsy|Cerebral_palsy|_spastic_quadriplegic|_3": 1,
    "Cerebral_palsy|_spastic_quadriplegic|_3|not_specified": 1,
    "ADD3-related_disorder": 1,
    "ADD3-related_disorder|not_provided": 2,
    "not_provided|ADD3-related_disorder": 2,
    "MXI1-related_disorder": 5,
    "Neurofibrosarcoma": 1,
    "Cornelia_de_Lange_syndrome_3": 329,
    "Cornelia_de_Lange_syndrome_3|not_provided": 7,
    "Cornelia_de_Lange_syndrome_3|Inborn_genetic_diseases": 6,
    "not_provided|not_specified|Cornelia_de_Lange_syndrome_3": 3,
    "SMC3-related_disorder|Cornelia_de_Lange_syndrome_3": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Cornelia_de_Lange_syndrome_3": 4,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_3|not_provided": 1,
    "SMC3-related_disorder": 15,
    "not_specified|Cornelia_de_Lange_syndrome_3": 3,
    "Cornelia_de_Lange_syndrome_3|not_specified|Inborn_genetic_diseases": 2,
    "Cornelia_de_Lange_syndrome_3|De_Lange_syndrome": 2,
    "not_specified|Cornelia_de_Lange_syndrome_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cornelia_de_Lange_syndrome_3": 2,
    "Cornelia_de_Lange_syndrome_3|SMC3-related_disorder": 3,
    "De_Lange_syndrome|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_3|not_specified": 1,
    "Cornelia_de_Lange_syndrome_3|Inborn_genetic_diseases|De_Lange_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_3|not_specified": 2,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_3": 11,
    "not_provided|Cornelia_de_Lange_syndrome_3": 5,
    "Cornelia_de_Lange_syndrome_3|De_Lange_syndrome|not_specified|not_provided": 1,
    "Cornelia_de_Lange_syndrome_3|SMC3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cornelia_de_Lange_syndrome_3|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|SMC3-related_disorder|Cornelia_de_Lange_syndrome_3": 1,
    "not_specified|not_provided|Cornelia_de_Lange_syndrome_3|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_3|not_specified|SMC3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_3|Intellectual_disability": 1,
    "Intellectual_disability|Cornelia_de_Lange_syndrome_3": 1,
    "not_specified|not_provided|Cornelia_de_Lange_syndrome_3": 2,
    "Cornelia_de_Lange_syndrome_3|Intellectual_disability|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Cornelia_de_Lange_syndrome_3": 1,
    "not_specified|not_provided|SMC3-related_disorder|Cornelia_de_Lange_syndrome_3": 1,
    "not_provided|SMC3-related_disorder|Inborn_genetic_diseases": 1,
    "SMC3-related_disorder|Inborn_genetic_diseases|not_provided|Cornelia_de_Lange_syndrome_3": 1,
    "not_provided|Cornelia_de_Lange_syndrome_3|Inborn_genetic_diseases": 1,
    "Cornelia_de_Lange_syndrome_3|Wiedemann-Steiner_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_3": 1,
    "Cornelia_de_Lange_syndrome_3|not_provided|not_specified": 1,
    "SMC3-related_disorder|not_provided|Cornelia_de_Lange_syndrome_3": 1,
    "Congenital_heart_disease|Neuromuscular_disease": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_3": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Cornelia_de_Lange_syndrome_3": 1,
    "Cornelia_de_Lange_syndrome_3|SMC3-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Dilated_cardiomyopathy_1DD|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 18,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 189,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 124,
    "Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype": 12,
    "Dilated_cardiomyopathy_1DD|not_provided": 39,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified": 7,
    "not_provided|Dilated_cardiomyopathy_1DD": 34,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided": 21,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 2,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD|Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided": 28,
    "not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified|RBM20-related_disorder": 1,
    "Dilated_cardiomyopathy_1DD|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1DD": 22,
    "not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified": 3,
    "not_specified|Dilated_cardiomyopathy_1DD": 23,
    "not_provided|not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|Primary_dilated_cardiomyopathy": 2,
    "not_specified|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 13,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 4,
    "Dilated_cardiomyopathy_1DD|not_specified|not_provided": 2,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 13,
    "not_specified|Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1DD|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1DD": 13,
    "Dilated_cardiomyopathy_1DD|not_specified": 20,
    "Cardiovascular_phenotype|RBM20-related_disorder|Dilated_cardiomyopathy_1DD": 1,
    "RBM20-related_disorder|Dilated_cardiomyopathy_1DD|not_specified|Cardiovascular_phenotype": 1,
    "Familial_dilated_cardiomyopathy_and_peripheral_neuropathy|Cardiovascular_phenotype|RBM20-related_disorder|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1DD": 5,
    "RBM20-related_disorder": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|Cardiomyopathy|RBM20-related_disorder": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_specified": 3,
    "Left_ventricular_noncompaction_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 2,
    "RBM20-related_disorder|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1DD|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 2,
    "not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1DD|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1DD|not_provided": 2,
    "Long_QT_syndrome|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 2,
    "not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 15,
    "Dilated_cardiomyopathy_1DD|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Ventricular_tachycardia|Pulmonary_valve_stenosis_(rare)|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|not_specified|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1A|not_specified|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 1,
    "RBM20-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_specified|not_provided": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "RBM20-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "RBM20-related_disorder|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|RBM20-related_disorder|Dilated_cardiomyopathy_1DD|Cardiomyopathy": 1,
    "RBM20-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|not_specified|Cardiovascular_phenotype": 6,
    "not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1DD": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1DD": 7,
    "not_specified|not_provided|Dilated_cardiomyopathy_1DD": 5,
    "RBM20-related_disorder|not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided|Cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1DD": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|RBM20-related_disorder|not_specified|not_provided|Cardiomyopathy|Conduction_disorder_of_the_heart|Dilated_cardiomyopathy_1DD": 1,
    "not_specified|Dilated_cardiomyopathy_1DD|not_provided": 5,
    "not_specified|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1DD": 1,
    "Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1DD": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 3,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 3,
    "not_provided|Dilated_cardiomyopathy_1DD|not_specified": 2,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 2,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|RBM20-related_disorder|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|RBM20-related_disorder|not_provided|Dilated_cardiomyopathy_1S|Dilated_cardiomyopathy_1A|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 2,
    "Dilated_cardiomyopathy_1DD|RBM20-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_specified|Dilated_cardiomyopathy_1DD": 1,
    "RBM20-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1DD": 3,
    "Dilated_cardiomyopathy_1DD|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1DD|Cardiomyopathy": 3,
    "Dilated_cardiomyopathy_1DD|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1DD|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1DD|not_specified": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|RBM20-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1DD|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|RBM20-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided|Cardiomyopathy|not_specified": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "Primary_dilated_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|not_specified|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|Dilated_cardiomyopathy_1A": 1,
    "not_provided|Cardiovascular_phenotype|sudden_unexplained_death_in_epilepsy|Hypertrophic_cardiomyopathy|Cardiac_arrest|Primary_dilated_cardiomyopathy|RBM20-related_disorder|Dilated_cardiomyopathy_1DD|Cardiomyopathy|not_specified": 1,
    "not_provided|RBM20-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|RBM20-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1DD|RBM20-related_disorder": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1DD": 1,
    "not_provided|Dilated_cardiomyopathy_1DD|RBM20-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_specified": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|RBM20-related_disorder": 1,
    "Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Dilated_cardiomyopathy_1DD": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified|Dilated_cardiomyopathy_1DD|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Heart_failure|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|not_specified": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1DD|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|not_specified": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD": 2,
    "Dilated_cardiomyopathy_1DD|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1DD|RBM20-related_disorder": 2,
    "not_provided|Dilated_cardiomyopathy_1DD|not_specified|Cardiovascular_phenotype": 1,
    "RBM20-related_disorder|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1DD|not_specified": 1,
    "Dilated_cardiomyopathy_1DD|not_specified|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1DD|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "RBM20-related_disorder|Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1DD": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1DD": 1,
    "Dilated_cardiomyopathy_1DD|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1DD|not_specified": 1,
    "BBIP1-related_disorder": 21,
    "BBIP1-related_disorder|not_provided|Bardet-Biedl_syndrome_18": 1,
    "BBIP1-related_disorder|not_provided": 6,
    "not_provided|BBIP1-related_disorder": 7,
    "not_provided|Bardet-Biedl_syndrome_18": 5,
    "Bardet-Biedl_syndrome_18|BBIP1-related_disorder|not_provided": 2,
    "Bardet-Biedl_syndrome_18": 3,
    "Bardet-Biedl_syndrome_18|not_provided": 3,
    "Bardet-Biedl_syndrome_18|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_18|BBIP1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_18|not_specified": 2,
    "BBIP1-related_disorder|not_provided|not_specified": 1,
    "BBIP1-related_disorder|Bardet-Biedl_syndrome_18|not_provided": 2,
    "Postaxial_hand_polydactyly|Rod-cone_dystrophy|Micropenis|Downslanted_palpebral_fissures|Narrow_forehead|Round_face|Specific_learning_disability|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Obesity|Flat_nasal_alae": 1,
    "BBIP1-related_disorder|not_specified|not_provided": 1,
    "BBIP1-related_disorder|Bardet-Biedl_syndrome_18": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 41,
    "not_specified|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 3,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 4,
    "Polycystic_kidney_disease_4|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|Pectus_excavatum|SHOC2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome-like_disorder_with_loose_anagen_hair|Inborn_genetic_diseases|not_provided|RASopathy|Noonan_syndrome": 1,
    "RASopathy|not_specified|not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|SHOC2-related_disorder": 1,
    "SHOC2-related_disorder": 5,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_provided": 3,
    "SHOC2-related_disorder|RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_provided": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|RASopathy|SHOC2-related_disorder|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|RASopathy|not_specified|not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "SHOC2-related_disorder|Cardiovascular_phenotype": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "not_specified|not_provided|RASopathy|Cardiovascular_phenotype": 5,
    "RASopathy|not_specified|Cardiovascular_phenotype|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_provided": 1,
    "not_specified|Noonan_syndrome": 48,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "RASopathy|SHOC2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_specified|RASopathy|Cardiovascular_phenotype": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|RASopathy|not_provided|SHOC2-related_disorder|Noonan_syndrome-like_disorder_with_loose_anagen_hair": 1,
    "Cardiovascular_phenotype|not_specified|Non-immune_hydrops_fetalis|RASopathy|not_provided|See_cases|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair": 1,
    "not_specified|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_provided|Cardiovascular_phenotype|RASopathy": 1,
    "RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|Cardiovascular_phenotype": 3,
    "RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 2,
    "not_provided|RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_specified": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|RASopathy": 3,
    "Noonan_syndrome|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_specified|not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair|SHOC2-related_disorder|RASopathy": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|RASopathy|not_specified|not_provided": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 2,
    "not_specified|RASopathy|not_provided|SHOC2-related_disorder|Cardiovascular_phenotype": 1,
    "RASopathy|SHOC2-related_disorder": 3,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "Cardiovascular_phenotype|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "Noonan_syndrome_3": 12,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_specified|RASopathy|SHOC2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_specified": 1,
    "RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|not_provided|SHOC2-related_disorder|RASopathy|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|RASopathy|not_provided": 4,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "not_provided|Noonan_syndrome_3|RASopathy|Cardiovascular_phenotype": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|not_specified": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|Noonan_syndrome_and_Noonan-related_syndrome|SHOC2-related_disorder|not_specified|not_provided|RASopathy": 1,
    "RASopathy|SHOC2-related_disorder|not_specified": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|SHOC2-related_disorder": 1,
    "not_specified|RASopathy|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1": 1,
    "RASopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "SHOC2-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 1,
    "Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|not_specified|RASopathy": 1,
    "SHOC2-related_disorder|RASopathy|Noonan_syndrome": 1,
    "not_specified|Noonan_syndrome-like_disorder_with_loose_anagen_hair_1|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "ADRA2A-related_disorder": 4,
    "not_specified|ADRA2A-related_disorder": 1,
    "Lipodystrophy|_familial_partial|_type_8": 1,
    "TECTB-related_disorder": 7,
    "Diarrhea_13": 1,
    "TCF7L2-related_disorder": 8,
    "TCF7L2-relatedIntellectual_disability|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|TCF7L2-related_disorder": 1,
    "TCF7L2-related_disorder|not_provided": 1,
    "Autism|not_provided": 7,
    "TCF7L2-related_Intellectual_disability": 1,
    "not_provided|TCF7L2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|TCF7L2-related_disorder": 1,
    "Factor_VII_Marburg_I_Variant_Thrombophilia": 60,
    "not_provided|Factor_VII_Marburg_I_Variant_Thrombophilia": 15,
    "Factor_VII_Marburg_I_Variant_Thrombophilia|not_provided": 3,
    "Factor_VII_Marburg_I_Variant_Thrombophilia|not_specified": 3,
    "Factor_VII_Marburg_I_Variant_Thrombophilia|HABP2-related_disorder|not_provided": 1,
    "Factor_VII_Marburg_I_Variant_Thrombophilia|not_specified|not_provided": 1,
    "HABP2-related_disorder": 4,
    "HABP2-related_disorder|not_provided|Factor_VII_Marburg_I_Variant_Thrombophilia": 3,
    "not_specified|Factor_VII_Marburg_I_Variant_Thrombophilia": 6,
    "HABP2-related_disorder|Thyroid_cancer|_nonmedullary|_5|Thrombophilia_due_to_thrombin_defect|Factor_VII_Marburg_I_Variant_Thrombophilia": 1,
    "Factor_VII_Marburg_I_Variant_Thrombophilia|HABP2-related_disorder": 3,
    "not_provided|not_specified|Factor_VII_Marburg_I_Variant_Thrombophilia": 1,
    "Thyroid_cancer|_nonmedullary|_5": 4,
    "Thrombophilia_due_to_thrombin_defect|Thyroid_cancer|_nonmedullary|_5|not_provided|Factor_VII_Marburg_I_Variant_Thrombophilia": 1,
    "not_provided|HABP2-related_disorder|Factor_VII_Marburg_I_Variant_Thrombophilia": 1,
    "not_provided|FACTOR_VII-ACTIVATING_PROTEASE_MARBURG_I_POLYMORPHISM|Thyroid_cancer|_nonmedullary|_5|THYROID_CANCER|_NONMEDULLARY|_5|_SUSCEPTIBILITY_TO|Factor_VII_Marburg_I_Variant_Thrombophilia|Venous_thromboembolism|_susceptibility_to": 1,
    "not_specified|not_provided|Factor_VII_Marburg_I_Variant_Thrombophilia": 1,
    "not_specified|NRAP-related_disorder|not_provided|Factor_VII_Marburg_I_Variant_Thrombophilia": 1,
    "NRAP-related_disorder": 26,
    "not_specified|NRAP-related_disorder": 3,
    "not_specified|not_provided|NRAP-related_disorder": 4,
    "not_specified|NRAP-related_disorder|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|NRAP-related_disorder": 2,
    "Cardiovascular_phenotype|NRAP-related_disorder": 4,
    "not_provided|NRAP-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|NRAP-related_disorder": 11,
    "Inborn_genetic_diseases|NRAP-related_disorder|not_specified": 1,
    "NRAP-related_disorder|not_provided|not_specified": 5,
    "NRAP-related_disorder|not_specified": 8,
    "NRAP-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "NRAP-related_disorder|not_specified|not_provided": 4,
    "NRAP-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "NRAP-related_disorder|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4": 22,
    "not_provided|NRAP-related_disorder|not_specified": 4,
    "NRAP-related_disorder|not_provided": 1,
    "Fibrosis|_neurodegeneration|_and_cerebral_angiomatosis": 14,
    "NHLRC2-related_disorder": 12,
    "Inborn_genetic_diseases|Fibrosis|_neurodegeneration|_and_cerebral_angiomatosis": 1,
    "not_provided|Fibrosis|_neurodegeneration|_and_cerebral_angiomatosis": 1,
    "Fibrosis|_neurodegeneration|_and_cerebral_angiomatosis|not_provided": 1,
    "Inborn_genetic_diseases|NHLRC2-related_disorder|not_provided": 1,
    "NHLRC2-related_disorder|not_provided": 2,
    "not_provided|NHLRC2-related_disorder|Inborn_genetic_diseases": 2,
    "Resting_heart_rate|not_specified|ADRB1-related_disorder|not_provided": 1,
    "SHORT_SLEEP|_FAMILIAL_NATURAL|_2": 1,
    "ADRB1-related_disorder|not_provided|Pulmonary_disease|_chronic_obstructive|_susceptibility_to": 1,
    "ADRB1-related_disorder": 1,
    "Growth_delay|Microcephaly|Developmental_stagnation|Seizure|Failure_to_thrive|EEG_with_spike-wave_complexes|Pulmonary_valve_stenosis|Severe_global_developmental_delay|Hypothyroidism|Relative_macrocephaly|not_provided": 1,
    "VWA2-related_disorder": 30,
    "VWA2-related_disorder|not_provided": 9,
    "not_provided|VWA2-related_disorder": 4,
    "GFRA1-related_disorder": 11,
    "Renal_hypodysplasia/aplasia_4": 5,
    "not_provided|GFRA1-related_disorder": 2,
    "not_provided|GFRA1-related_disorder|not_specified": 1,
    "GFRA1-related_disorder|not_provided": 1,
    "not_provided|PNLIP-related_disorder": 2,
    "not_specified|PNLIP-related_disorder|not_provided": 1,
    "not_provided|Pancreatic_triacylglycerol_lipase_deficiency": 2,
    "Pancreatic_triacylglycerol_lipase_deficiency": 2,
    "PNLIP-related_disorder|not_provided": 1,
    "PNLIP-related_disorder": 1,
    "Microphthalmia|_syndromic_11": 25,
    "VAX1-related_disorder|Microphthalmia|_syndromic_11": 4,
    "Microphthalmia|_syndromic_11|not_specified|not_provided": 1,
    "Microphthalmia|_syndromic_11|not_provided": 1,
    "Microphthalmia|_syndromic_11|not_specified": 1,
    "Microphthalmia|_syndromic_11|VAX1-related_disorder": 1,
    "VAX1-related_disorder|not_provided|Microphthalmia|_syndromic_11": 1,
    "not_specified|Microphthalmia|_syndromic_11": 2,
    "not_provided|VAX1-related_disorder": 1,
    "not_provided|Microphthalmia|_syndromic_11": 1,
    "KCNK18-related_disorder": 3,
    "not_provided|KCNK18-related_disorder": 2,
    "not_provided|Migraine|_with_or_without_aura|_susceptibility_to|_13": 1,
    "Migraine|_with_or_without_aura|_susceptibility_to|_13|not_specified|Parkinson_disease|Vascular_parkinsonism|Parkinsonian_disorder|KCNK18-related_disorder|not_provided": 1,
    "KCNK18-related_disorder|not_provided": 3,
    "Migraine|_with_or_without_aura|_susceptibility_to|_13": 2,
    "KCNK18-related_neurodevelopmental_disorder": 1,
    "not_specified|KCNK18-related_disorder": 1,
    "not_specified|Migraine|_with_or_without_aura|_susceptibility_to|_13": 1,
    "not_provided|Brain_dopamine-serotonin_vesicular_transport_disease": 5,
    "SLC18A2-related_disorder|not_provided": 2,
    "Brain_dopamine-serotonin_vesicular_transport_disease|not_provided": 1,
    "Brain_dopamine-serotonin_vesicular_transport_disease": 8,
    "not_provided|SLC18A2-related_disorder": 3,
    "Brain_dopamine-serotonin_vesicular_transport_disease|not_specified|not_provided": 1,
    "not_specified|SLC18A2-related_disorder|not_provided": 1,
    "Abnormal_dense_granules|Abnormal_dense_granule_content|Brain_dopamine-serotonin_vesicular_transport_disease": 1,
    "Intellectual_developmental_disorder_with_autism_and_dysmorphic_facies": 3,
    "Intellectual_developmental_disorder_with_autism_and_dysmorphic_facies|not_specified": 1,
    "Congenital_hypogonadotropic_hypogonadism": 7,
    "EMX2-related_disorder": 1,
    "not_provided|Schizencephaly": 1,
    "Schizencephaly|EMX2-related_disorder|not_specified": 1,
    "not_provided|Congenital_hypogonadotropic_hypogonadism|EMX2-related_disorder": 1,
    "NANOS1-related_disorder|Spermatogenic_failure_12|not_provided": 1,
    "not_provided|NANOS1-related_disorder": 1,
    "Spermatogenic_failure_12": 2,
    "NANOS1-related_disorder": 2,
    "NANOS1-related_disorder|not_provided": 1,
    "SFXN4-related_disorder": 3,
    "Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome": 8,
    "Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome|not_provided": 4,
    "not_specified|not_provided|SFXN4-related_disorder": 1,
    "Inborn_genetic_diseases|Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome": 1,
    "not_provided|Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome|not_specified": 1,
    "not_provided|SFXN4-related_disorder": 1,
    "not_provided|Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome": 2,
    "Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome|not_provided": 1,
    "Growth_and_developmental_delay-hypotonia-vision_impairment-lactic_acidosis_syndrome|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive_32": 8,
    "Corneal_dystrophy|_punctiform_and_polychromatic_pre-descemet": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_autosomal_recessive_32": 2,
    "Spinocerebellar_ataxia|_autosomal_recessive_32|not_provided": 1,
    "Autosomal_recessive_cerebellar_ataxia|not_provided|Spinocerebellar_ataxia|_autosomal_recessive_32|Corneal_dystrophy|_punctiform_and_polychromatic_pre-descemet": 1,
    "GRK5-related_disorder": 2,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 264,
    "not_provided|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 17,
    "not_specified|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 2,
    "Dilated_cardiomyopathy_1HH|not_provided|not_specified|Myofibrillar_myopathy_6": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1HH": 12,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 14,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 330,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 37,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 40,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|Cardiovascular_phenotype": 9,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 38,
    "Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 8,
    "not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_specified": 2,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified": 6,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 8,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified": 4,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided": 1,
    "See_cases|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype": 27,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_provided": 5,
    "not_specified|not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 3,
    "not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided": 10,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 7,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided": 15,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|BAG3-related_disorder|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|BAG3-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified": 5,
    "not_provided|not_specified|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_fibrillation|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|Cardiomyopathy": 1,
    "not_specified|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|not_provided|Cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy": 1,
    "BAG3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 2,
    "not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 15,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|not_specified": 3,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 6,
    "Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|Myofibrillar_myopathy_6|not_specified": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|BAG3-related_disorder": 1,
    "Dilated_cardiomyopathy_1HH|Primary_dilated_cardiomyopathy|not_provided|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 3,
    "BAG3-related_disorder|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|BAG3-related_disorder": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|not_provided": 3,
    "not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_6|not_specified|not_provided|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Myofibrillar_myopathy_6|BAG3-related_disorder|Dilated_cardiomyopathy_1HH|Left_ventricular_noncompaction_1|Cardiovascular_phenotype": 1,
    "not_provided|BAG3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiomyopathy|not_provided|Myofibrillar_Myopathy|_Dominant|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 3,
    "BAG3-related_disorder|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 7,
    "BAG3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiovascular_phenotype": 5,
    "Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 3,
    "BAG3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|BAG3-related_disorder|not_provided": 1,
    "Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|Cardiomyopathy|not_provided": 1,
    "BAG3-related_disorder|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Myofibrillar_Myopathy|_Dominant": 2,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|Myofibrillar_myopathy_6": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "Primary_dilated_cardiomyopathy|Myocarditis|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "Cardiomyopathy|Premature_ventricular_contraction|BAG3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|BAG3-related_disorder|Abnormality_of_the_musculature": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Peripheral_neuropathy": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|Cardiovascular_phenotype": 3,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|BAG3-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "BAG3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|not_provided": 3,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|BAG3-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 2,
    "Myofibrillar_myopathy|not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Elevated_circulating_creatine_kinase_concentration|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Primary_familial_dilated_cardiomyopathy|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "BAG3-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 2,
    "BAG3-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|BAG3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|Primary_dilated_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 2,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified": 1,
    "BAG3-related_disorder|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Myofibrillar_Myopathy|_Dominant|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided": 1,
    "not_provided|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified": 1,
    "Myofibrillar_myopathy_6|not_provided|not_specified|Dilated_cardiomyopathy_1HH": 1,
    "Primary_dilated_cardiomyopathy|Myocarditis|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|BAG3-related_disorder": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified": 1,
    "not_specified|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_provided": 1,
    "Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "Dilated_cardiomyopathy_1HH|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_6|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Atrial_fibrillation": 1,
    "not_provided|BAG3-related_disorder|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1HH|not_provided|Cardiovascular_phenotype|Myofibrillar_myopathy_6": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Long_QT_syndrome": 1,
    "Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1HH|not_specified|Cardiovascular_phenotype|Myofibrillar_myopathy_6|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH": 1,
    "BAG3-related_disorder|Cardiovascular_phenotype|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided": 1,
    "BAG3-related_disorder": 2,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_specified": 2,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_specified|BAG3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_6|Primary_dilated_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1HH": 1,
    "Dilated_cardiomyopathy_1HH|not_provided": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|Cardiovascular_phenotype": 1,
    "BAG3-related_disorder|Myofibrillar_myopathy_6|not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1HH": 1,
    "not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|BAG3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_15": 1,
    "Myofibrillar_myopathy_6": 1,
    "Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|Myofibrillar_Myopathy|_Dominant|not_provided|Long_QT_syndrome": 1,
    "Myofibrillar_myopathy_6|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1HH|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Myofibrillar_myopathy_6|Dilated_cardiomyopathy_1HH|not_provided": 1,
    "Dilated_cardiomyopathy_1HH|Myofibrillar_myopathy_6|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Myofibrillar_Myopathy|_Dominant": 2,
    "not_provided|SEC23IP-related_disorder": 3,
    "SEC23IP-related_disorder": 18,
    "WDR11-related_disorder": 9,
    "not_specified|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 9,
    "Hypogonadotropic_hypogonadism_14_with_or_without_anosmia|not_provided": 3,
    "WDR11-related_disorder|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Intellectual_developmental_disorder|_autosomal_recessive_78|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia|Intellectual_developmental_disorder|_autosomal_recessive_78|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 7,
    "Intellectual_developmental_disorder|_autosomal_recessive_78": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_78|Microcephaly": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_78|Microcephaly|WDR11-related_disorder": 1,
    "not_provided|WDR11-related_disorder": 4,
    "Hypogonadotropic_hypogonadism_14_with_anosmia|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_14_with_or_without_anosmia|Intellectual_developmental_disorder|_autosomal_recessive_78": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_78|Microcephaly": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_78|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 1,
    "not_provided|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_recessive_78|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 1,
    "not_specified|WDR11-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_78|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_14_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_14_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis": 2,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Pfeiffer_syndrome|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome": 1,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 17,
    "Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis": 1,
    "Isolated_Coronal_Synostosis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Beare-Stevenson_cutis_gyrata_syndrome": 8,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome": 1,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome": 3,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Levy-Hollister_syndrome|Pfeiffer_syndrome|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome": 1,
    "Isolated_Coronal_Synostosis|Crouzon_syndrome|Craniosynostosis_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 3,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|not_provided|Crouzon_syndrome|Saethre-Chotzen_syndrome": 2,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Acrocephalosyndactyly_type_I": 1,
    "Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 7,
    "FGFR2-related_disorder": 16,
    "not_specified|Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 1,
    "Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|FGFR2-related_disorder|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis": 1,
    "Craniosynostosis_syndrome|Levy-Hollister_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Acrocephalosyndactyly_type_I|FGFR2-related_disorder|not_provided|Saethre-Chotzen_syndrome": 1,
    "FGFR2-related_craniosynostosis": 247,
    "Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|FGFR2-related_craniosynostosis": 1,
    "Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Gastric_cancer|FGFR2-related_craniosynostosis": 1,
    "not_provided|FGFR2-related_craniosynostosis": 24,
    "Craniosynostosis_syndrome|FGFR2-related_craniosynostosis|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Crouzon_syndrome": 2,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 3,
    "Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|LADD_syndrome_1|Jackson-Weiss_syndrome|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer": 31,
    "FGFR2-related_craniosynostosis|not_specified": 1,
    "FGFR2-related_craniosynostosis|FGFR2-related_disorder|not_provided": 1,
    "Isolated_Coronal_Synostosis|not_provided|Saethre-Chotzen_syndrome|FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Craniosynostosis_syndrome|not_specified": 1,
    "FGFR2-related_craniosynostosis|not_provided": 16,
    "Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Jackson-Weiss_syndrome|LADD_syndrome_1|not_provided|FGFR2-related_craniosynostosis": 1,
    "FGFR2-related_craniosynostosis|not_provided|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Pfeiffer_syndrome": 1,
    "not_specified|FGFR2-related_craniosynostosis": 6,
    "FGFR2-related_craniosynostosis|not_provided|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|FGFR2-related_disorder": 1,
    "Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis": 2,
    "not_provided|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Crouzon_syndrome|Gastric_cancer|Bent_bone_dysplasia_syndrome_1": 3,
    "not_provided|FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Jackson-Weiss_syndrome|LADD_syndrome_1": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Crouzon_syndrome": 1,
    "Pfeiffer_syndrome|FGFR2-related_craniosynostosis": 2,
    "FGFR2-related_craniosynostosis|Acrocephalosyndactyly_type_I|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type": 1,
    "not_specified|FGFR2-related_disorder|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Gastric_cancer|FGFR2-related_craniosynostosis": 1,
    "not_provided|FGFR2-related_craniosynostosis|Inborn_genetic_diseases|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|LADD_syndrome_1|Gastric_cancer": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|not_provided": 1,
    "Acrocephalosyndactyly_type_I": 4,
    "FGFR2-related_craniosynostosis|not_provided|Levy-Hollister_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type": 1,
    "not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|FGFR2-related_craniosynostosis|Crouzon_syndrome|Craniosynostosis_syndrome|not_specified|Saethre-Chotzen_syndrome": 1,
    "not_provided|Pfeiffer_syndrome": 1,
    "FGFR2-related_disorder|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Pfeiffer_syndrome|not_provided|FGFR2-related_craniosynostosis": 1,
    "FGFR2-related_craniosynostosis|not_specified|not_provided": 4,
    "Pfeiffer_syndrome|Acrocephalosyndactyly_type_I|Bent_bone_dysplasia_syndrome_1|LADD_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|FGFR2-related_craniosynostosis": 1,
    "Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|LADD_syndrome_1|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|FGFR2-related_craniosynostosis|Isolated_Coronal_Synostosis": 1,
    "FGFR2-related_craniosynostosis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Pfeiffer_syndrome|not_provided": 1,
    "FGFR2-related_craniosynostosis|Inborn_genetic_diseases": 3,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Jackson-Weiss_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome|Pfeiffer_syndrome|FGFR2-related_disorder": 1,
    "Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|not_provided": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis": 5,
    "Craniosynostosis_syndrome|Intellectual_disability|Seizure": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Gastric_cancer|FGFR2-related_craniosynostosis|not_provided": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|not_provided|Pfeiffer_syndrome": 1,
    "FGFR2-related_craniosynostosis|FGFR2-related_disorder": 3,
    "Pemigatinib_resistance|Crouzon_syndrome": 1,
    "Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|LADD_syndrome_1|Pfeiffer_syndrome|not_provided": 1,
    "FGFR2-related_craniosynostosis|not_provided|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Crouzon_syndrome": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_specified|Isolated_Coronal_Synostosis|not_provided|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome": 1,
    "Craniosynostosis_syndrome|Inborn_genetic_diseases|FGFR2-related_craniosynostosis|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Crouzon_syndrome": 1,
    "Levy-Hollister_syndrome|FGFR2-related_craniosynostosis": 1,
    "Acrocephalosyndactyly_type_I|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Pfeiffer_syndrome|FGFR2-related_craniosynostosis": 1,
    "Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Gastric_cancer|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Levy-Hollister_syndrome|Crouzon_syndrome|FGFR2-related_craniosynostosis": 2,
    "Craniosynostosis_syndrome|FGFR2-related_craniosynostosis|not_specified|not_provided|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Isolated_Coronal_Synostosis": 1,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|LADD_syndrome_1|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer": 2,
    "not_specified|FGFR2-related_craniosynostosis|not_provided": 1,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Jackson-Weiss_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome|Pfeiffer_syndrome": 1,
    "Inborn_genetic_diseases|LADD_syndrome_1|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|FGFR2-related_craniosynostosis|not_provided": 1,
    "not_provided|FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|LADD_syndrome_1": 1,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Gastric_cancer|Jackson-Weiss_syndrome": 2,
    "Beare-Stevenson_cutis_gyrata_syndrome|Gastric_cancer|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|FGFR2-related_craniosynostosis": 1,
    "Inborn_genetic_diseases|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Gastric_cancer|Jackson-Weiss_syndrome|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome|LADD_syndrome_1|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis": 2,
    "Crouzon_syndrome": 6,
    "FGFR2-related_craniosynostosis|Autosomal_dominant_syndrome_including_deafness": 1,
    "Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Saethre-Chotzen_syndrome|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Levy-Hollister_syndrome|Jackson-Weiss_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|Pfeiffer_syndrome|FGFR2-related_craniosynostosis|Inborn_genetic_diseases": 1,
    "FGFR2-related_disorder|Craniosynostosis_syndrome|FGFR2-related_craniosynostosis|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer": 1,
    "Isolated_Coronal_Synostosis|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|LADD_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Craniosynostosis_syndrome": 1,
    "not_provided|Bent_bone_dysplasia_syndrome_1": 1,
    "not_provided|FGFR2-related_craniosynostosis|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Crouzon_syndrome|Gastric_cancer|Bent_bone_dysplasia_syndrome_1": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Neoplasm_of_stomach|Bent_bone_dysplasia_syndrome_1": 1,
    "not_provided|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "FGFR2-related_disorder|Inborn_genetic_diseases|not_provided|Bent_bone_dysplasia_syndrome_1": 1,
    "LADD_syndrome_1|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Gastric_cancer": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Familial_scaphocephaly_syndrome|_McGillivray_type|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|Levy-Hollister_syndrome|Bent_bone_dysplasia_syndrome_1|Neoplasm_of_stomach|Pfeiffer_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|not_provided|Endometrial_carcinoma": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "not_provided|FGFR2-related_craniosynostosis|FGFR2-related_disorder|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Gastric_cancer": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Gastric_cancer|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|LADD_syndrome_1": 3,
    "Saethre-Chotzen_syndrome|not_provided": 1,
    "FGFR2-related_craniosynostosis|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|not_provided": 1,
    "Crouzon_syndrome|not_provided|FGFR2-related_craniosynostosis": 1,
    "Acrocephalosyndactyly_type_I|FGFR2-related_craniosynostosis": 1,
    "Inborn_genetic_diseases|FGFR2-related_craniosynostosis|not_provided|Crouzon_syndrome|See_cases": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|not_provided|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome_type_3|Crouzon_syndrome|Pfeiffer_syndrome": 1,
    "Hydrocephalus|Mild_fetal_ventriculomegaly|Lateral_ventricle_dilatation|Hypointensity_of_cerebral_white_matter_on_MRI|Short_neck|Abnormal_posterior_cranial_fossa_morphology|Shallow_orbits|Deviated_nasal_septum|Facial_asymmetry|High_forehead|Choanal_stenosis|Brachyturricephaly|Abnormal_zygomatic_bone_morphology|Cranial_asymmetry|Low-set_ears|Hypertelorism|Abnormal_pinna_morphology|Wide_anterior_fontanel|Downslanted_palpebral_fissures|Flat_occiput|High_palate|Narrow_forehead|FGFR2-related_craniosynostosis|not_provided|Meier-Gorlin_syndrome_1|Crouzon_syndrome|Pfeiffer_syndrome": 1,
    "FGFR2-related_disorder|Gastric_cancer|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Acrocephalosyndactyly_type_I|Levy-Hollister_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Jackson-Weiss_syndrome|Bent_bone_dysplasia_syndrome_1|Saethre-Chotzen_syndrome|FGFR2-related_craniosynostosis|not_provided|Craniosynostosis_syndrome|Neoplasm_of_stomach|Craniosynostosis|_nonclassifiable_autosomal_dominant|Scaphocephaly_and_axenfeld-rieger_anomaly": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|Crouzon_syndrome|Jackson-Weiss_syndrome|Pfeiffer_syndrome": 1,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|LADD_syndrome_1": 2,
    "FGFR2-related_craniosynostosis|Crouzon_syndrome": 3,
    "FGFR2-related_craniosynostosis|not_provided|Crouzon_syndrome": 5,
    "FGFR2-related_craniosynostosis|not_provided|Jackson-Weiss_syndrome": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|Pfeiffer_syndrome|Jackson-Weiss_syndrome|not_provided|Crouzon_syndrome": 1,
    "Jackson-Weiss_syndrome|LADD_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|Acrocephalosyndactyly_type_I|Bent_bone_dysplasia_syndrome_1|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Crouzon_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|FGFR2-related_craniosynostosis|Neoplasm_of_stomach|Levy-Hollister_syndrome|Craniosynostosis_syndrome|not_provided": 1,
    "FGFR2-related_syndromic_and_non-syndromic_craniosynostoses|FGFR2-related_craniosynostosis|not_provided|Pfeiffer_syndrome": 1,
    "FGFR2-related_craniosynostosis|not_provided|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Crouzon_syndrome": 1,
    "FGFR2-related_craniosynostosis|not_provided|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Jackson-Weiss_syndrome|Pfeiffer_syndrome": 1,
    "FGFR2-related_craniosynostosis|not_provided|Pfeiffer_syndrome": 1,
    "not_provided|Pfeiffer_syndrome|FGFR2-related_craniosynostosis": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Pfeiffer_syndrome|Neoplasm_of_stomach|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|FGFR2-related_craniosynostosis": 1,
    "Crouzon_syndrome|FGFR2-related_craniosynostosis": 1,
    "Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Neoplasm_of_stomach|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_provided|LADD_syndrome_1|Gastric_cancer|Isolated_Coronal_Synostosis": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Jackson-Weiss_syndrome|Bent_bone_dysplasia_syndrome_1|Familial_scaphocephaly_syndrome|_McGillivray_type|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|LADD_syndrome_1|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer|Craniosynostosis_syndrome": 1,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Gastric_cancer|LADD_syndrome_1|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Jackson-Weiss_syndrome": 1,
    "FGFR2-related_craniosynostosis|Pfeiffer_syndrome": 3,
    "not_provided|FGFR2-related_disorder|FGFR2-related_craniosynostosis": 3,
    "Gastric_cancer|Crouzon_syndrome|Acrocephalosyndactyly_type_I|Familial_scaphocephaly_syndrome|_McGillivray_type|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|Levy-Hollister_syndrome|Bent_bone_dysplasia_syndrome_1|Pfeiffer_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|FGFR2-related_craniosynostosis|not_provided|Craniosynostosis|_nonsyndromic_unicoronal": 1,
    "not_provided|LADD_syndrome_1|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Gastric_cancer": 1,
    "FGFR2-related_craniosynostosis|Jackson-Weiss_syndrome|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Pfeiffer_syndrome|LADD_syndrome_1|Gastric_cancer|not_provided": 1,
    "FGFR2-related_craniosynostosis|Acrocephalosyndactyly_type_I": 1,
    "not_provided|FGFR2-related_disorder": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_provided|not_specified|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 1,
    "not_provided|Crouzon_syndrome": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "Levy-Hollister_syndrome|Pfeiffer_syndrome|Acrocephalosyndactyly_type_I|Bent_bone_dysplasia_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|Jackson-Weiss_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|FGFR2-related_craniosynostosis": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Acrocephalosyndactyly_type_I|LADD_syndrome_1|Gastric_cancer": 1,
    "Bent_bone_dysplasia_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|Crouzon_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|FGFR2-related_craniosynostosis|not_provided|Craniofacial-skeletal-dermatologic_dysplasia": 1,
    "FGFR2-related_disorder|not_provided|Aural_atresia|_congenital|Pfeiffer_syndrome": 1,
    "FGFR2-related_disorder|not_provided|Crouzon_syndrome": 1,
    "FGFR2-related_craniosynostosis|Inborn_genetic_diseases|not_provided|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Crouzon_syndrome": 1,
    "FGFR2-related_disorder|not_provided|FGFR2-related_craniosynostosis|Crouzon_syndrome": 1,
    "FGFR2-related_disorder|not_provided|FGFR2-related_craniosynostosis|Crouzon_syndrome|Pfeiffer_syndrome": 1,
    "not_provided|FGFR2-related_craniosynostosis|Crouzon_syndrome": 1,
    "Inborn_genetic_diseases|FGFR2-related_craniosynostosis": 2,
    "FGFR2-related_craniosynostosis|Gastric_cancer|not_provided|Crouzon_syndrome|Pfeiffer_syndrome": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Levy-Hollister_syndrome|Crouzon_syndrome|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I": 1,
    "Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|FGFR2-related_disorder|FGFR2-related_craniosynostosis|Saethre-Chotzen_syndrome": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Jackson-Weiss_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Isolated_Coronal_Synostosis|Craniosynostosis_syndrome|FGFR2-related_craniosynostosis": 1,
    "Inborn_genetic_diseases|Acrocephalosyndactyly_type_I|FGFR2-related_craniosynostosis": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|Neoplasm_of_stomach|Crouzon_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|not_provided": 1,
    "Pfeiffer_syndrome_variant": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|not_specified|not_provided|Crouzon_syndrome": 1,
    "FGFR2-related_disorder|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Crouzon_syndrome|Jackson-Weiss_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Pfeiffer_syndrome|LADD_syndrome_1|Inborn_genetic_diseases|FGFR2-related_craniosynostosis|not_provided|Endometrial_carcinoma": 1,
    "Jackson-Weiss_syndrome|Gastric_cancer|Acrocephalosyndactyly_type_I|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|FGFR2-related_craniosynostosis|not_specified": 1,
    "Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "not_specified|Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|FGFR2-related_craniosynostosis|not_provided|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Craniosynostosis_syndrome": 1,
    "FGFR2-related_disorder|Craniosynostosis_syndrome|FGFR2-related_craniosynostosis|not_specified|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_specified|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|LADD_syndrome_1|Jackson-Weiss_syndrome|Crouzon_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer": 1,
    "not_specified|FGFR2-related_craniosynostosis|Inborn_genetic_diseases": 1,
    "not_provided|FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|LADD_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Jackson-Weiss_syndrome": 1,
    "Inborn_genetic_diseases|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|LADD_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Jackson-Weiss_syndrome": 1,
    "Inborn_genetic_diseases|FGFR2-related_craniosynostosis|not_provided": 1,
    "not_provided|Isolated_Coronal_Synostosis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "not_provided|FGFR2-related_craniosynostosis|Inborn_genetic_diseases": 1,
    "not_provided|FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Gastric_cancer": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Acrocephalosyndactyly_type_I|LADD_syndrome_1|Gastric_cancer|not_specified|FGFR2-related_craniosynostosis": 1,
    "Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Gastric_cancer|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Pfeiffer_syndrome|FGFR2-related_craniosynostosis": 1,
    "not_provided|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Gastric_cancer": 1,
    "Crouzon_syndrome|Acrocephalosyndactyly_type_I|Inborn_genetic_diseases|not_provided|FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Neoplasm_of_stomach|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|not_specified|not_provided|Isolated_Coronal_Synostosis|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 3,
    "FGFR2-related_craniosynostosis|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Gastric_cancer|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|LADD_syndrome_1|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|not_provided": 1,
    "FGFR2-related_craniosynostosis|not_provided|FGFR2-related_disorder|FGFR2-realated_disorder|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Levy-Hollister_syndrome|Acrocephalosyndactyly_type_I|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Gastric_cancer": 1,
    "FGFR2-related_craniosynostosis|Inborn_genetic_diseases|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|Levy-Hollister_syndrome|Crouzon_syndrome|Gastric_cancer|Bent_bone_dysplasia_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|FGFR2-related_craniosynostosis": 1,
    "Isolated_Coronal_Synostosis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|FGFR2-related_disorder|FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "FGFR2-related_craniosynostosis|Inborn_genetic_diseases|Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Pfeiffer_syndrome|LADD_syndrome_1|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Acrocephalosyndactyly_type_I|Gastric_cancer|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Jackson-Weiss_syndrome": 1,
    "Bent_bone_dysplasia_syndrome_1|Crouzon_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Beare-Stevenson_cutis_gyrata_syndrome|Gastric_cancer|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|LADD_syndrome_1|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Saethre-Chotzen_syndrome|FGFR2-related_craniosynostosis|Inborn_genetic_diseases": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Bent_bone_dysplasia_syndrome_1|Jackson-Weiss_syndrome|Levy-Hollister_syndrome|Pfeiffer_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Acrocephalosyndactyly_type_I|Gastric_cancer|Craniosynostosis|_nonspecific|FGFR2-related_craniosynostosis": 1,
    "FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Levy-Hollister_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Acrocephalosyndactyly_type_I": 1,
    "FGFR2-related_craniosynostosis|not_specified|not_provided|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 1,
    "Crouzon_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 1,
    "Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Gastric_cancer|Beare-Stevenson_cutis_gyrata_syndrome|LADD_syndrome_1|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Crouzon_syndrome|Jackson-Weiss_syndrome|Bent_bone_dysplasia_syndrome_1|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|FGFR2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|LADD_syndrome_1|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Gastric_cancer|Bent_bone_dysplasia_syndrome_1": 1,
    "FGFR2-related_disorder|Crouzon_syndrome|Pfeiffer_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Beare-Stevenson_cutis_gyrata_syndrome|LADD_syndrome_1|Jackson-Weiss_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|FGFR2-related_craniosynostosis|not_provided|not_specified": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|FGFR2-related_craniosynostosis|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis": 1,
    "FGFR2-related_disorder|FGFR2-related_craniosynostosis|not_specified|Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I|Jackson-Weiss_syndrome|Pfeiffer_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Levy-Hollister_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Craniosynostosis_syndrome|not_specified|not_provided|Isolated_Coronal_Synostosis": 1,
    "FGFR2-related_craniosynostosis|Beare-Stevenson_cutis_gyrata_syndrome|Pfeiffer_syndrome|Bent_bone_dysplasia_syndrome_1|Gastric_cancer|Levy-Hollister_syndrome|Crouzon_syndrome|Jackson-Weiss_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Acrocephalosyndactyly_type_I|Inborn_genetic_diseases": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Bent_bone_dysplasia_syndrome_1|Acrocephalosyndactyly_type_I|Pfeiffer_syndrome|Levy-Hollister_syndrome|Antley-Bixler_syndrome_without_genital_anomalies_or_disordered_steroidogenesis|Gastric_cancer|Jackson-Weiss_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Familial_scaphocephaly_syndrome|_McGillivray_type|Isolated_Coronal_Synostosis|Craniosynostosis_syndrome": 1,
    "not_provided|Crouzon_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 1,
    "Craniosynostosis_syndrome|not_provided|Isolated_Coronal_Synostosis|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 1,
    "not_provided|Isolated_Coronal_Synostosis|Crouzon_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "Craniosynostosis_syndrome|not_specified|not_provided|Isolated_Coronal_Synostosis|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome": 1,
    "Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Isolated_Coronal_Synostosis": 3,
    "Isolated_Coronal_Synostosis|Saethre-Chotzen_syndrome|Craniosynostosis_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Crouzon_syndrome": 1,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Levy-Hollister_syndrome|Pfeiffer_syndrome|Jackson-Weiss_syndrome|Crouzon_syndrome|Beare-Stevenson_cutis_gyrata_syndrome|Acrocephalosyndactyly_type_I|Saethre-Chotzen_syndrome": 1,
    "Craniosynostosis_syndrome|Isolated_Coronal_Synostosis|Beare-Stevenson_cutis_gyrata_syndrome|Saethre-Chotzen_syndrome|Crouzon_syndrome": 2,
    "Isolated_Coronal_Synostosis|Crouzon_syndrome|Craniosynostosis_syndrome|Saethre-Chotzen_syndrome|Beare-Stevenson_cutis_gyrata_syndrome": 1,
    "ATE1-related_disorder": 9,
    "Age_related_macular_degeneration_8": 11,
    "not_provided|Age_related_macular_degeneration_8": 1,
    "Age_related_macular_degeneration_8|not_specified": 1,
    "ARMS2-related_disorder|not_provided|Age_related_macular_degeneration_8": 2,
    "not_provided|Age_related_macular_degeneration_8|Macular_degeneration": 5,
    "Age_related_macular_degeneration_8|not_provided": 2,
    "Age_related_macular_degeneration_7": 2,
    "not_provided|not_specified|Macular_degeneration": 2,
    "HTRA1-related_disorder": 9,
    "CARASIL_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2": 3,
    "not_provided|HTRA1-related_disorder": 2,
    "not_specified|not_provided|CARASIL_syndrome|Macular_degeneration": 2,
    "HTRA1-related_autosomal_dominant_cerebral_small_vessel_disease": 1,
    "not_provided|CARASIL_syndrome|Macular_degeneration": 2,
    "CARASIL_syndrome": 6,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2": 20,
    "HTRA1-related_autosomal_dominant_cerebral_small_vessel_disease|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Macular_degeneration|HTRA1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Macular_degeneration": 1,
    "CARASIL_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|not_specified|HTRA1-related_disorder|not_provided|Macular_degeneration": 1,
    "not_specified|CARASIL_syndrome": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|not_provided": 4,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|CARASIL_syndrome|Cerebral_arterial_disease": 1,
    "Macular_degeneration|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CARASIL_syndrome": 3,
    "CARASIL_syndrome|not_provided": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|CARASIL_syndrome|not_provided": 1,
    "HTRA1-related_disorder|not_provided": 3,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|CARASIL_syndrome": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|CARASIL_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|Age_related_macular_degeneration_7": 1,
    "Inborn_genetic_diseases|Macular_degeneration": 1,
    "HTRA1-related_cerebral_small_vessel_disease|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|not_provided|Vascular_dementia": 1,
    "HTRA1-related_cerebral_small_vessel_disease|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|CARASIL_syndrome|not_provided": 1,
    "not_provided|Macular_degeneration|not_specified": 1,
    "Small_vessel_cerebrovascular_disease|Seizure|Personality_changes|Cognitive_impairment|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|not_provided|CARASIL_syndrome": 1,
    "CARASIL_syndrome|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2": 2,
    "HTRA1-related_disorder|not_provided|Age_related_macular_degeneration_7": 1,
    "Vascular_dementia|not_provided|CARASIL_syndrome": 1,
    "not_provided|Age_related_macular_degeneration_7": 1,
    "HTRA1-related_cerebral_small_vessel_disease|not_provided|CARASIL_syndrome": 1,
    "HTRA1-related_cerebral_small_vessel_disease|HTRA1-related_disorder|CARASIL_syndrome": 1,
    "not_specified|Macular_degeneration|not_provided": 1,
    "Macular_degeneration|HTRA1-related_disorder": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_2|not_specified|not_provided|CARASIL_syndrome|Macular_degeneration": 2,
    "not_provided|HTRA1-related_disorder|Inborn_genetic_diseases|CARASIL_syndrome|Macular_degeneration": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|not_provided": 6,
    "DMBT1-related_disorder": 33,
    "not_provided|DMBT1-related_disorder": 6,
    "DMBT1-related_disorder|not_provided": 3,
    "DMBT1-related_disorder|not_specified|not_provided": 1,
    "not_specified|DMBT1-related_disorder": 3,
    "Thrombocytopenia_7": 9,
    "IKZF5-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_29": 2,
    "not_provided|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 23,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|not_provided": 18,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 219,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|ACADSB-related_disorder": 3,
    "not_provided|ACADSB-related_disorder|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 1,
    "not_provided|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|ACADSB-related_disorder": 1,
    "ACADSB-related_disorder|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 5,
    "ACADSB-related_disorder|not_provided|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 2,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|See_cases": 2,
    "ACADSB-related_disorder": 5,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|not_provided|ACADSB-related_disorder": 1,
    "not_specified|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|not_specified": 1,
    "not_provided|Deficiency_of_2-methylbutyryl-CoA_dehydrogenase|not_specified": 1,
    "HMX2-related_disorder": 1,
    "BUB3-related_disorder": 1,
    "not_specified|BUB3-related_disorder": 2,
    "Ornithine_aminotransferase_deficiency": 547,
    "not_provided|Ornithine_aminotransferase_deficiency": 12,
    "not_specified|not_provided|Ornithine_aminotransferase_deficiency": 2,
    "Ornithine_aminotransferase_deficiency|Hyperornithinemia": 4,
    "Ornithine_aminotransferase_deficiency|OAT-related_disorder": 3,
    "Ornithine_aminotransferase_deficiency|Inborn_genetic_diseases": 17,
    "Inborn_genetic_diseases|Ornithine_aminotransferase_deficiency": 11,
    "Hyperornithinemia|Ornithine_aminotransferase_deficiency": 7,
    "not_provided|Ornithine_aminotransferase_deficiency|OAT-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|Ornithine_aminotransferase_deficiency": 1,
    "Ornithine_aminotransferase_deficiency|Retinal_dystrophy|not_provided": 1,
    "not_specified|Ornithine_aminotransferase_deficiency": 2,
    "not_specified|Ornithine_aminotransferase_deficiency|Retinal_dystrophy": 1,
    "Ornithine_aminotransferase_deficiency|Retinal_dystrophy": 1,
    "OAT-related_disorder|Ornithine_aminotransferase_deficiency": 1,
    "Gyrate_atrophy_of_choroid_and_retina_with_pyridoxine-responsive_ornithinemia|Ornithine_aminotransferase_deficiency": 1,
    "Hyperornithinemia": 1,
    "Retinal_dystrophy|not_provided|Ornithine_aminotransferase_deficiency": 1,
    "Optic_atrophy|Abnormal_choroid_morphology|Visual_field_defect|Pain|Ornithine_aminotransferase_deficiency": 1,
    "not_provided|Ornithine_aminotransferase_deficiency|Retinal_dystrophy": 1,
    "Hyperornithinemia|Gyrate_atrophy_of_choroid_and_retina_with_pyridoxine-responsive_ornithinemia|Ornithine_aminotransferase_deficiency": 1,
    "Ornithine_aminotransferase_deficiency|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Ornithine_aminotransferase_deficiency|not_provided|not_specified": 1,
    "Retinal_dystrophy|Ornithine_aminotransferase_deficiency": 1,
    "OAT-related_disorder|not_specified|Ornithine_aminotransferase_deficiency": 1,
    "not_provided|not_specified|Ornithine_aminotransferase_deficiency": 1,
    "Ornithine_aminotransferase_deficiency|not_specified": 1,
    "OAT-related_disorder|Inborn_genetic_diseases|not_provided|Ornithine_aminotransferase_deficiency": 1,
    "Retinal_dystrophy|Ornithine_aminotransferase_deficiency|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Ornithine_aminotransferase_deficiency": 1,
    "Ornithine_aminotransferase_deficiency|not_specified|Retinal_dystrophy": 1,
    "CTBP2-related_disorder": 27,
    "CTBP2-related_disorder|not_provided": 3,
    "not_provided|CTBP2-related_disorder": 2,
    "Heterotaxy|_visceral|_7|_autosomal|Inborn_genetic_diseases": 1,
    "Heterotaxy|_visceral|_7|_autosomal": 18,
    "Visceral_heterotaxy|not_provided|Heterotaxy|_visceral|_7|_autosomal": 1,
    "MMP21-related_disorder": 11,
    "MMP21-related_disorder|not_provided": 4,
    "Heterotaxy|_visceral|_7|_autosomal|not_provided|Visceral_heterotaxy": 1,
    "MMP21-related_disorder|Heterotaxy|_visceral|_7|_autosomal": 1,
    "not_provided|Heterotaxy|_visceral|_7|_autosomal": 4,
    "Heterotaxy|_visceral|_7|_autosomal|MMP21-related_disorder": 2,
    "not_provided|MMP21-related_disorder|Heterotaxy|_visceral|_7|_autosomal": 1,
    "Cutaneous_porphyria": 34,
    "not_provided|Cutaneous_porphyria": 10,
    "UROS-related_disorder|not_provided": 2,
    "Cutaneous_porphyria|not_provided": 5,
    "UROS-related_disorder|not_provided|Cutaneous_porphyria": 2,
    "UROS-related_disorder": 3,
    "Cutaneous_porphyria|not_provided|UROS-related_disorder|not_specified": 1,
    "Cutaneous_porphyria|Inborn_genetic_diseases": 1,
    "not_provided|UROS-related_disorder": 1,
    "UROS-related_disorder|Cutaneous_porphyria|not_provided": 1,
    "Inborn_genetic_diseases|Cutaneous_porphyria": 1,
    "not_provided|UROS-related_disorder|Cutaneous_porphyria": 1,
    "not_provided|Cutaneous_porphyria|UROS-related_disorder": 1,
    "not_specified|Cutaneous_porphyria|not_provided": 1,
    "Thyroid_tumor": 1,
    "Abnormal_circulating_immunoglobulin_concentration": 1,
    "not_specified|Temporomandibular_joint_disorder": 1,
    "DOCK1-related_disorder": 1,
    "MKI67-related_disorder": 10,
    "not_specified|MKI67-related_disorder": 1,
    "not_specified|MKI67-related_disorder|not_provided": 1,
    "MKI67-related_disorder|not_provided": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome": 67,
    "not_provided|EBF3-related_disorder": 1,
    "EBF3-related_disorder": 19,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Intellectual_disability|_X-linked_102|Hypotonia|_ataxia|_and_delayed_development_syndrome": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Intellectual_disability|not_provided": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|EBF3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "EBF3-related_disorder|Intellectual_disability": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|EBF3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hypotonia|_ataxia|_and_delayed_development_syndrome": 5,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|not_provided": 5,
    "not_provided|Hypotonia|_ataxia|_and_delayed_development_syndrome|Inborn_genetic_diseases": 1,
    "See_cases|Inborn_genetic_diseases|not_provided|Hypotonia|_ataxia|_and_delayed_development_syndrome": 1,
    "Neurodevelopmental_disorder|Hypotonia|_ataxia|_and_delayed_development_syndrome|not_provided": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Renal_tubular_dysgenesis|Developmental_regression|Generalized_hypotonia|Broad-based_gait|Neurogenic_bladder|not_provided": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Intellectual_disability|Expressive_language_delay|Ataxia|Global_developmental_delay|Hypotonia|not_provided": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Intellectual_disability|Expressive_language_delay|Ataxia|Global_developmental_delay|Hypotonia|Inborn_genetic_diseases|not_provided|Isolated_Pierre-Robin_syndrome": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|not_provided|Intellectual_disability": 1,
    "EBF3-related_disorder|not_provided": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|not_specified": 1,
    "Hypotonia|_ataxia|_and_delayed_development_syndrome|Vesicoureteral_reflux|Recurrent_urinary_tract_infections|Global_developmental_delay|Generalized_hypotonia|Constipation|Abnormal_facial_shape|Growth_abnormality": 1,
    "not_provided|Spastic_ataxia_8|_autosomal_recessive|_with_hypomyelinating_leukodystrophy": 3,
    "Spastic_ataxia_8|_autosomal_recessive|_with_hypomyelinating_leukodystrophy": 21,
    "Spastic_ataxia_8|_autosomal_recessive|_with_hypomyelinating_leukodystrophy|not_provided": 4,
    "NKX6-2-related_disorder": 1,
    "TUBGCP2-related_disorder": 10,
    "Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures|not_specified": 1,
    "not_provided|TUBGCP2-related_disorder": 8,
    "Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures|not_provided": 2,
    "Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures|Abnormality_of_neuronal_migration": 2,
    "not_specified|TUBGCP2-related_disorder|not_provided": 1,
    "Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures": 6,
    "not_specified|Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures": 1,
    "not_provided|Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures": 4,
    "not_specified|TUBGCP2-related_disorder": 2,
    "TUBGCP2-related_disorder|not_provided": 2,
    "not_provided|Abnormality_of_neuronal_migration|Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures": 1,
    "Abnormality_of_neuronal_migration|not_specified|Pachygyria|_microcephaly|_developmental_delay|_and_dysmorphic_facies|_with_or_without_seizures|not_provided": 1,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 32,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided": 14,
    "ECHS1-related_disorder|not_provided": 4,
    "not_provided|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 14,
    "Inborn_genetic_diseases|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided": 1,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 1,
    "not_provided|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_specified": 1,
    "ECHS1-related_disorder": 3,
    "not_provided|ECHS1-related_disorder": 4,
    "not_provided|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|Inborn_genetic_diseases": 1,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided|ECHS1-related_disorder": 1,
    "not_provided|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|See_cases": 1,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 1,
    "not_specified|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided": 1,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided|not_specified": 1,
    "ECHS1-related_disorder|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 1,
    "not_provided|ECHS1-related_disorder|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 2,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|Leigh_syndrome|not_provided|See_cases": 1,
    "ECHS1-related_disorder|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 1,
    "Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency|not_provided|Leigh_syndrome": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_short-chain_Enoyl-Coa_hydratase_1_deficiency": 1,
    "CYP2E1*6_ALLELE": 1,
    "SYCE1-related_disorder": 5,
    "Premature_ovarian_failure_12": 1,
    "Spermatogenic_failure_15": 1,
    "SIRT3-related_disorder": 9,
    "not_provided|SIRT3-related_disorder": 1,
    "PSMD13-related_disorder": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_5": 1,
    "IFITM5-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Osteogenesis_imperfecta_type_5": 2,
    "Osteogenesis_imperfecta_type_5|not_provided": 3,
    "not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_5|not_provided": 1,
    "IFITM5-related_disorder|not_provided|Osteogenesis_imperfecta_type_5": 1,
    "not_provided|IFITM5-related_disorder": 2,
    "not_provided|Osteogenesis_imperfecta|not_specified": 1,
    "Inborn_genetic_diseases|IFITM5-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_5": 1,
    "Osteogenesis_imperfecta|IFITM5-related_disorder|not_provided": 1,
    "IFITM5-related_disorder|Inborn_genetic_diseases|Osteogenesis_imperfecta|not_provided": 1,
    "IFITM5-related_disorder|not_provided|Osteogenesis_imperfecta_type_5|Osteogenesis_imperfecta|Postmenopausal_osteoporosis": 1,
    "Influenza|_severe|_susceptibility_to": 2,
    "Encephalitis|_acute|_infection-induced|_susceptibility_to|_12|RNH1-related_disorder": 1,
    "Encephalitis|_acute|_infection-induced|_susceptibility_to|_12": 5,
    "RNH1-related_disorder|Encephalitis|_acute|_infection-induced|_susceptibility_to|_12": 1,
    "Encephalitis|_acute|_infection-induced|_susceptibility_to|_12|not_specified": 1,
    "not_provided|HRAS-related_disorder|not_specified": 1,
    "Linear_nevus_sebaceous_syndrome|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Epidermal_nevus": 1,
    "Noonan_syndrome|Costello_syndrome": 3,
    "Large_congenital_melanocytic_nevus|Epidermal_nevus|Thyroid_cancer|_nonmedullary|_2|Costello_syndrome|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|not_specified": 1,
    "Costello_syndrome|not_provided": 17,
    "not_provided|Cardiovascular_phenotype|Costello_syndrome": 6,
    "HRAS-related_disorder|not_provided|Costello_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Thyroid_cancer|_nonmedullary|_2|Linear_nevus_sebaceous_syndrome|Costello_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|HRAS-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|RASopathy": 1,
    "Costello_syndrome|Cardiovascular_phenotype|Noonan_syndrome": 1,
    "Intellectual_disability|Costello_syndrome": 1,
    "not_provided|Costello_syndrome": 12,
    "Costello_syndrome|not_specified": 9,
    "RASopathy|Costello_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Thyroid_cancer|_nonmedullary|_2|Linear_nevus_sebaceous_syndrome|Costello_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|not_provided": 1,
    "HRAS-related_disorder|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Epidermal_nevus|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Epidermal_nevus|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Costello_syndrome": 1,
    "Costello_syndrome|HRAS-related_disorder": 2,
    "Linear_nevus_sebaceous_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|Costello_syndrome|Thyroid_cancer|_nonmedullary|_2": 1,
    "not_provided|HRAS-related_disorder|Costello_syndrome": 1,
    "Costello_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Linear_nevus_sebaceous_syndrome|Epidermal_nevus|Thyroid_cancer|_nonmedullary|_2|Large_congenital_melanocytic_nevus": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Costello_syndrome|RASopathy|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Costello_syndrome": 19,
    "Costello_syndrome|not_provided|not_specified": 2,
    "Costello_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "HRAS-related_disorder|Costello_syndrome": 3,
    "Cardiovascular_phenotype|not_provided|Costello_syndrome": 1,
    "not_specified|Costello_syndrome": 10,
    "Costello_syndrome|not_provided|Cardiovascular_phenotype": 3,
    "Epidermolytic_nevus": 1,
    "HRAS-related_disorder|not_provided": 1,
    "HRAS-related_disorder": 6,
    "not_provided|RASopathy|Costello_syndrome|HRAS-related_disorder": 1,
    "Congenital_fibrosis_of_extraocular_muscles|not_provided|Costello_syndrome": 1,
    "not_specified|Costello_syndrome|not_provided": 1,
    "Costello_syndrome|Cardiovascular_phenotype": 18,
    "Costello_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Thyroid_cancer|_nonmedullary|_2|Linear_nevus_sebaceous_syndrome|Costello_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|Cardiovascular_phenotype|HRAS-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|RASopathy": 1,
    "Linear_nevus_sebaceous_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|Costello_syndrome|Thyroid_cancer|_nonmedullary|_2|Cardiovascular_phenotype": 1,
    "Costello_syndrome|not_provided|not_specified|Cardiovascular_phenotype|Linear_nevus_sebaceous_syndrome": 1,
    "not_provided|Intellectual_disability|not_specified|Costello_syndrome": 1,
    "Large_congenital_melanocytic_nevus|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Thyroid_cancer|_nonmedullary|_2|Linear_nevus_sebaceous_syndrome|not_provided": 1,
    "HRAS-related_disorder|not_specified|Costello_syndrome": 1,
    "not_specified|not_provided|Costello_syndrome|RASopathy|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Costello_syndrome|Cardiovascular_phenotype|not_provided": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|Costello_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Costello_syndrome": 1,
    "Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Epidermal_nevus|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|not_specified|not_provided": 1,
    "Costello_syndrome|not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "Costello_syndrome|Ovarian_cancer": 1,
    "Cardiovascular_phenotype|Costello_syndrome|not_specified": 2,
    "Linear_nevus_sebaceous_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Cardiovascular_phenotype|HRAS-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|RASopathy": 1,
    "not_provided|RASopathy|Costello_syndrome": 1,
    "Thyroid_cancer|_nonmedullary|_2|Linear_nevus_sebaceous_syndrome|Costello_syndrome|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|Cardiovascular_phenotype|HRAS-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Costello_syndrome|not_provided": 1,
    "Costello_syndrome|HRAS-related_disorder|RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_specified|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Large_congenital_melanocytic_nevus|Linear_nevus_sebaceous_syndrome|Epidermal_nevus|Thyroid_cancer|_nonmedullary|_2|RASopathy|HRAS-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Costello_syndrome|HRAS-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Hypophosphatemic_rickets|Parathyroid_gland_adenoma": 1,
    "Costello_syndrome|RASopathy|not_provided|Pulmonic_stenosis|Supravalvar_aortic_stenosis": 1,
    "HRAS-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome|Costello_syndrome": 1,
    "Costello_syndrome|HRAS-related_disorder|Cardiovascular_phenotype|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "HRAS-related_disorder|Costello_syndrome|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "HRAS-related_disorder|Vascular_malformation": 1,
    "Cardiovascular_phenotype|Costello_syndrome|not_specified|HRAS-related_disorder": 1,
    "Myopathy|_congenital|_with_excess_of_muscle_spindles|not_provided|Costello_syndrome": 2,
    "KA-like_vemurafenib-induced_squamous_lesions|Lip_and_oral_cavity_carcinoma|Costello_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Malignant_tumor_of_urinary_bladder|Costello_syndrome|Epidermal_nevus|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Linear_nevus_sebaceous_syndrome|Vascular_Tumors_Including_Pyogenic_Granuloma|Salivary_gland_neoplasm|not_provided": 1,
    "Thyroid_cancer|_nonmedullary|_2|Lip_and_oral_cavity_carcinoma|not_provided|Epidermal_nevus|Spermatocytic_seminoma|Noonan_syndrome_3": 1,
    "Malignant_tumor_of_urinary_bladder|Costello_syndrome|Thyroid_cancer|_nonmedullary|_2|Large_congenital_melanocytic_nevus|Linear_nevus_sebaceous_syndrome|Epidermal_nevus|not_provided": 1,
    "Intramuscular_hemangioma": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Costello_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Costello_syndrome": 1,
    "not_specified|Costello_syndrome|Non-small_cell_lung_carcinoma|RASopathy": 1,
    "HRAS-related_disorder|not_provided|RASopathy|Costello_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Costello_syndrome|not_specified": 1,
    "Costello_syndrome|HRAS-related_disorder|not_specified": 1,
    "Costello_syndrome|Vascular_Tumors_Including_Pyogenic_Granuloma": 2,
    "not_specified|Cardiovascular_phenotype|Costello_syndrome|not_provided": 1,
    "Costello_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Costello_syndrome": 1,
    "Cardiovascular_phenotype|Costello_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Vascular_Tumors_Including_Pyogenic_Granuloma": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Costello_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Costello_syndrome|Squamous_cell_lung_carcinoma|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Costello_syndrome": 2,
    "not_specified|not_provided|Costello_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Costello_syndrome|not_specified|HRAS-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Costello_syndrome": 1,
    "Lip_and_oral_cavity_carcinoma|KA-like_vemurafenib-induced_squamous_lesions|Large_congenital_melanocytic_nevus|not_provided|Linear_nevus_sebaceous_syndrome|Costello_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Costello_syndrome|Linear_nevus_sebaceous_syndrome|HRAS-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Non-immune_hydrops_fetalis": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|HRAS-related_disorder|Linear_nevus_sebaceous_syndrome|Thyroid_cancer|_nonmedullary|_2|Costello_syndrome|Large_congenital_melanocytic_nevus|Epidermal_nevus|Malignant_tumor_of_urinary_bladder|not_provided|RASopathy|Noonan_syndrome": 1,
    "cutaneous-skeletal_hypophosphatemia_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|HRAS-related_disorder|Lip_and_oral_cavity_carcinoma|NEVUS_SPILUS|_SOMATIC|SPITZ_NEVUS|_SOMATIC|Linear_nevus_sebaceous_syndrome|Nevus_sebaceous|Non-immune_hydrops_fetalis|Epidermal_nevus|Costello_syndrome": 1,
    "HRAS-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Costello_syndrome": 1,
    "HRAS-related_disorder|Cardiovascular_phenotype|not_provided|Costello_syndrome|Myopathy|_congenital|_with_excess_of_muscle_spindles|Malignant_tumor_of_urinary_bladder|Epidermal_nevus": 1,
    "Costello_syndrome|Linear_nevus_sebaceous_syndrome|Thyroid_cancer|_nonmedullary|_2|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|Epidermal_nevus|Noonan_syndrome_and_Noonan-related_syndrome|Inborn_genetic_diseases|Rhabdomyosarcoma|not_provided": 1,
    "HRAS-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Lip_and_oral_cavity_carcinoma|not_provided|Nevus_sebaceous|RASopathy|Non-immune_hydrops_fetalis|Costello_syndrome|Costello_syndrome|_severe": 1,
    "Malignant_tumor_of_urinary_bladder|Epidermal_nevus|Large_congenital_melanocytic_nevus|Thyroid_cancer|_nonmedullary|_2|Costello_syndrome|Linear_nevus_sebaceous_syndrome|Nevus_sebaceous|not_provided|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|HRAS-related_disorder|Epidermal_nevus|Thyroid_cancer|_nonmedullary|_2|Costello_syndrome|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Large_congenital_melanocytic_nevus|Lip_and_oral_cavity_carcinoma|Wooly_hair_nevus|Rhabdomyosarcoma|not_provided|Nevus_sebaceous|RASopathy|Epidermal_nevus_with_urothelial_cancer|_somatic|Noonan_syndrome_1|Myopathy|_congenital|_with_excess_of_muscle_spindles|See_cases": 1,
    "not_specified|Large_congenital_melanocytic_nevus|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Thyroid_cancer|_nonmedullary|_2|Epidermal_nevus|Costello_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Costello_syndrome|not_specified|not_provided": 1,
    "not_provided|LRRC56-related_disorder|Ciliary_dyskinesia|_primary|_39": 3,
    "not_provided|Ciliary_dyskinesia|_primary|_39": 6,
    "not_provided|LRRC56-related_disorder": 12,
    "Ciliary_dyskinesia|_primary|_39": 5,
    "LRRC56-related_disorder|not_provided": 18,
    "Ciliary_dyskinesia|_primary|_39|LRRC56-related_disorder|not_provided": 2,
    "Ciliary_dyskinesia|_primary|_39|not_provided|LRRC56-related_disorder": 4,
    "LRRC56-related_disorder": 3,
    "not_specified|LRRC56-related_disorder|not_provided": 1,
    "LRRC56-related_disorder|not_provided|Ciliary_dyskinesia|_primary|_39": 1,
    "LRRC56-related_disorder|not_specified|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_39|not_provided": 1,
    "LRRC56-related_disorder|not_provided|not_specified": 2,
    "LRRC56-related_disorder|Ciliary_dyskinesia|_primary|_39|not_provided": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_39|LRRC56-related_disorder": 1,
    "not_specified|PHRF1-related_disorder": 2,
    "PHRF1-related_disorder": 5,
    "PHRF1-related_disorder|not_provided": 1,
    "Immunodeficiency_39": 572,
    "Immunodeficiency_39|not_provided": 4,
    "Immunodeficiency_39|not_specified": 42,
    "IRF7-related_disorder|Immunodeficiency_39": 3,
    "not_provided|Immunodeficiency_39": 6,
    "not_specified|Immunodeficiency_39|not_provided": 3,
    "not_specified|not_provided|Immunodeficiency_39": 8,
    "not_specified|Immunodeficiency_39": 22,
    "Immunodeficiency_39|not_provided|not_specified": 1,
    "Immunodeficiency_39|IRF7-related_disorder": 4,
    "not_specified|IRF7-related_disorder|Immunodeficiency_39|not_provided": 1,
    "IRF7-related_disorder|not_provided|Immunodeficiency_39": 1,
    "IRF7-related_disorder": 2,
    "not_specified|not_provided|IRF7-related_disorder|Immunodeficiency_39": 1,
    "Immunodeficiency_39|not_provided|IRF7-related_disorder": 1,
    "methamphetamine_use_disorder": 1,
    "Hereditary_attention_deficit-hyperactivity_disorder": 9,
    "not_provided|DRD4-related_disorder": 3,
    "DRD4-related_disorder": 15,
    "DRD4-related_disorder|not_provided": 3,
    "AUTONOMIC_NERVOUS_SYSTEM_DYSFUNCTION|not_provided|DRD4-related_disorder|not_specified": 1,
    "DRD4-related_disorder|not_specified": 2,
    "not_provided|DRD4_POLYMORPHISM": 1,
    "not_specified|DRD4-related_disorder": 2,
    "Hereditary_attention_deficit-hyperactivity_disorder|not_provided": 2,
    "DRD4-related_disorder|Hereditary_attention_deficit-hyperactivity_disorder": 1,
    "not_specified|Hereditary_attention_deficit-hyperactivity_disorder|not_provided|DRD4-related_disorder": 1,
    "not_specified|Hereditary_attention_deficit-hyperactivity_disorder": 2,
    "DEAF1-related_disorder": 9,
    "Intellectual_disability|_autosomal_dominant_24": 40,
    "DEAF1-related_disorder|not_provided": 9,
    "Intellectual_disability|_autosomal_dominant_24|not_provided|See_cases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_24": 9,
    "Intellectual_disability|_autosomal_dominant_24|not_provided": 5,
    "Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 2,
    "Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome|not_provided": 1,
    "Intellectual_disability-epilepsy-extrapyramidal_syndrome": 10,
    "Intellectual_disability-epilepsy-extrapyramidal_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Prostate_cancer|not_provided": 1,
    "Intellectual_disability-epilepsy-extrapyramidal_syndrome|Intellectual_disability|_autosomal_dominant_24|not_provided": 2,
    "not_provided|Intellectual_disability-epilepsy-extrapyramidal_syndrome|Intellectual_disability|_autosomal_dominant_24": 6,
    "not_provided|DEAF1-related_disorder": 9,
    "Inborn_genetic_diseases|DEAF1-related_disorder|Intellectual_disability-epilepsy-extrapyramidal_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|DEAF1-related_disorder": 1,
    "DEAF1-related_disorder|not_specified|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_24|not_provided|Inborn_genetic_diseases": 1,
    "DEAF1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_24|DEAF1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_24|not_provided|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome|DEAF1-related_disorder|not_specified|not_provided": 1,
    "DEAF1-related_disorder|Intellectual_disability|_autosomal_dominant_24|not_provided": 1,
    "not_provided|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 5,
    "Intellectual_disability-epilepsy-extrapyramidal_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "DEAF1-related_disorder|not_provided|Autism_spectrum_disorder|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 1,
    "Intellectual_disability-epilepsy-extrapyramidal_syndrome|not_provided|Obesity|Attention_deficit_hyperactivity_disorder|Poor_fine_motor_coordination|Floppy_infant|Thin_upper_lip_vermilion|Tooth_malposition|Malar_flattening|Mandibular_prognathia|Delayed_speech_and_language_development": 1,
    "not_provided|Developmental_disorder|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome|not_provided|Neurodevelopmental_delay": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_24|Inborn_genetic_diseases": 2,
    "DEAF1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DEAF1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_24|Intellectual_disability-epilepsy-extrapyramidal_syndrome|Inborn_genetic_diseases": 1,
    "DEAF1-related_disorder|not_provided|Intellectual_disability-epilepsy-extrapyramidal_syndrome|Intellectual_disability|_autosomal_dominant_24|not_specified": 1,
    "not_specified|Meniere_disease|not_provided": 1,
    "EPS8L2-related_disorder": 11,
    "Hearing_loss|_autosomal_recessive_106|not_provided": 3,
    "not_provided|EPS8L2-related_disorder": 10,
    "Hearing_loss|_autosomal_recessive_106": 13,
    "not_provided|Hearing_loss|_autosomal_recessive_106": 2,
    "EPS8L2-related_disorder|not_specified|not_provided": 2,
    "EPS8L2-related_disorder|Hearing_loss|_autosomal_recessive_106": 1,
    "EPS8L2-related_disorder|not_provided": 3,
    "not_provided|Meniere_disease|not_specified": 1,
    "not_specified|not_provided|EPS8L2-related_disorder|Hearing_loss|_autosomal_recessive_106": 1,
    "Deficiency_of_transaldolase": 32,
    "not_provided|Deficiency_of_transaldolase": 13,
    "not_provided|TALDO1-related_disorder": 12,
    "Deficiency_of_transaldolase|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|TALDO1-related_disorder": 1,
    "TALDO1-related_disorder|not_provided": 8,
    "Inborn_genetic_diseases|not_provided|TALDO1-related_disorder|Deficiency_of_transaldolase": 3,
    "TALDO1-related_disorder|not_provided|Deficiency_of_transaldolase": 1,
    "TALDO1-related_disorder": 15,
    "not_provided|Cataract|Severe_global_developmental_delay|Microcephaly": 1,
    "TALDO1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|TALDO1-related_disorder": 1,
    "Deficiency_of_transaldolase|TALDO1-related_disorder|not_provided": 1,
    "not_provided|TALDO1-related_disorder|Deficiency_of_transaldolase": 1,
    "Inborn_genetic_diseases|Deficiency_of_transaldolase": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive": 17,
    "Developmental_and_epileptic_encephalopathy|_3": 14,
    "SLC25A22-related_disorder|not_provided|Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_3|SLC25A22-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Early_myoclonic_encephalopathy": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_3": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Early_myoclonic_encephalopathy": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|Early_myoclonic_encephalopathy": 1,
    "Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Early_myoclonic_encephalopathy": 2,
    "Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_3|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Early_myoclonic_encephalopathy": 2,
    "SLC25A22-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Early_myoclonic_encephalopathy": 5,
    "Developmental_delay|Macrocephaly|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|Early_myoclonic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_3": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Early_myoclonic_encephalopathy|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_3|Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy": 1,
    "SLC25A22-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|SLC25A22-related_disorder|not_specified|not_provided|Early_myoclonic_encephalopathy": 1,
    "not_specified|not_provided|SLC25A22-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_3|Inborn_genetic_diseases|SLC25A22-related_disorder|not_specified|not_provided|Early_myoclonic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_3|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_specified|Early_myoclonic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_3": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Early_myoclonic_encephalopathy": 1,
    "Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Early_myoclonic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Early_myoclonic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Early_myoclonic_encephalopathy": 1,
    "not_provided|Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy|_3|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_3": 1,
    "not_provided|Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_3|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_3": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Early_myoclonic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Early_myoclonic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_3|Developmental_and_epileptic_encephalopathy|Early_myoclonic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_3|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_3|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|SLC25A22-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Early_myoclonic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_3|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Inborn_genetic_diseases|Early_myoclonic_encephalopathy|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_3|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Seizure|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive": 1,
    "PIDD1-related_disorder": 15,
    "Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly": 18,
    "Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly|Intellectual_disability": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly|not_provided": 2,
    "PIDD1-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_3|Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly": 1,
    "not_provided|PIDD1-associated_neurodevelopmental_disorder|Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly|PIDD1-related_disorder|Inborn_genetic_diseases": 1,
    "PIDD1-related_disorder|Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly": 1,
    "not_provided|PIDD1-related_disorder": 1,
    "not_provided|PIDD1-related_disorder|Inborn_genetic_diseases": 1,
    "PIDD1-associated_neurodevelopmental_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_75|_with_neuropsychiatric_features_and_variant_lissencephaly|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|PIDD1-related_disorder": 1,
    "Neutral_lipid_storage_myopathy": 469,
    "Neutral_lipid_storage_myopathy|not_provided": 8,
    "not_provided|Neutral_lipid_storage_myopathy": 21,
    "Abnormality_of_the_musculature|Neutral_lipid_storage_myopathy": 1,
    "Inborn_genetic_diseases|Neutral_lipid_storage_myopathy": 20,
    "Neutral_lipid_storage_myopathy|Inborn_genetic_diseases": 19,
    "Neutral_lipid_storage_myopathy|PNPLA2-related_disorder": 6,
    "not_provided|Neutral_lipid_storage_myopathy|not_specified": 4,
    "Neutral_lipid_storage_myopathy|not_specified": 3,
    "not_specified|not_provided|Neutral_lipid_storage_myopathy": 4,
    "PNPLA2-related_disorder|Neutral_lipid_storage_myopathy": 5,
    "Inborn_genetic_diseases|not_provided|Neutral_lipid_storage_myopathy": 3,
    "not_specified|Neutral_lipid_storage_myopathy|not_provided": 6,
    "not_provided|Neutral_lipid_storage_myopathy|Inborn_genetic_diseases": 2,
    "Neutral_lipid_storage_myopathy|not_provided|not_specified": 3,
    "PNPLA2-related_disorder|Neutral_lipid_storage_myopathy|Inborn_genetic_diseases": 1,
    "Neutral_lipid_storage_myopathy|not_provided|PNPLA2-related_disorder": 1,
    "Neutral_lipid_storage_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "Neutral_lipid_storage_myopathy|PNPLA2-related_disorder|not_provided": 2,
    "not_specified|Neutral_lipid_storage_myopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neutral_lipid_storage_myopathy|not_specified": 1,
    "Inborn_genetic_diseases|Neutral_lipid_storage_myopathy|not_provided": 1,
    "Neutral_lipid_storage_myopathy|not_specified|not_provided": 1,
    "Neutral_lipid_storage_myopathy|See_cases": 1,
    "Neutral_lipid_storage_myopathy|Inborn_genetic_diseases|PNPLA2-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM": 9,
    "Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM|not_provided": 8,
    "Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness": 4,
    "not_provided|CD151-related_disorder": 6,
    "CD151-related_disorder|not_provided": 3,
    "Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM": 20,
    "not_provided|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness": 1,
    "Inborn_genetic_diseases|RAPH_BLOOD_GROUP_SYSTEM|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM": 2,
    "RAPH_BLOOD_GROUP_SYSTEM|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM": 1,
    "CD151-related_disorder": 1,
    "not_provided|RAPH_BLOOD_GROUP_SYSTEM|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM": 1,
    "not_provided|Inborn_genetic_diseases|RAPH_BLOOD_GROUP_SYSTEM|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness": 1,
    "Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|not_provided": 2,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_7|_with_nephropathy_and_deafness|RAPH_BLOOD_GROUP_SYSTEM|not_provided": 3,
    "MUC6-related_disorder": 1,
    "Susceptibility_to_coronavirus_disease_(COVID-19)_severity_and_mortality_due_to_low_plasma_levels_of_MUC5B|Antisynthetase_syndrome|not_provided|Interstitial_lung_disease_2|Pulmonary_fibrosis|_idiopathic|_susceptibility_to": 1,
    "MUC5B-related_disorder": 7,
    "not_specified|MUC5B-related_disorder": 1,
    "Interstitial_lung_disease_2|not_specified|not_provided": 1,
    "not_specified|Interstitial_lung_disease_2": 4,
    "not_provided|MUC5B-related_disorder": 2,
    "MUC5B-related_disorder|not_specified": 1,
    "Interstitial_lung_disease_2|not_provided": 1,
    "not_provided|not_specified|Interstitial_lung_disease_2": 2,
    "MUC5B-related_disorder|not_provided": 1,
    "not_specified|MUC5B-related_disorder|not_provided": 1,
    "MUC5B-related_disorder|not_specified|not_provided": 1,
    "Interstitial_lung_disease_2|Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Chronic_obstructive_pulmonary_disease|Combined_pulmonary_fibrosis-emphysema_syndrome": 1,
    "Interstitial_lung_disease_2|Chronic_obstructive_pulmonary_disease": 1,
    "Inborn_genetic_diseases|BRSK2-related_disorder": 2,
    "BRSK2-related_disorder": 38,
    "not_provided|BRSK2-related_disorder": 12,
    "BRSK2-related_disorder|not_provided": 7,
    "BRSK2-associated_neurodevelopmental_disorder": 1,
    "BRSK2-related_Intellectual_Disability_and_Autism": 1,
    "Inborn_genetic_diseases|BRSK2-related_disorder|not_provided": 1,
    "BRSK2-related_disorder|Inborn_genetic_diseases": 1,
    "BRSK2-related_disorder|not_specified|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_10": 36,
    "Neuronal_ceroid_lipofuscinosis_10|not_provided": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_10": 3,
    "Neuronal_ceroid_lipofuscinosis_10|not_specified|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_10|not_provided|not_specified": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Inborn_genetic_diseases": 8,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_10": 2,
    "Neuronal_ceroid_lipofuscinosis|not_specified|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_10": 2,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 8,
    "Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis": 7,
    "Severe_microlissencephaly|Exaggerated_startle_response": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 3,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases": 3,
    "Neuronal_ceroid_lipofuscinosis|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_10": 1,
    "Neuronal_ceroid_lipofuscinosis_10|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 1,
    "Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis|not_provided|not_specified": 1,
    "CTSD-related_disorder|Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "not_provided|CTSD-related_disorder|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "CTSD-related_disorder|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 6,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10|Inborn_genetic_diseases|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_10": 1,
    "CTSD-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 1,
    "CTSD-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_specified": 2,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_10|not_specified": 1,
    "CTSD-related_disorder|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10|not_specified|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Neuronal_ceroid_lipofuscinosis_10|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_10|not_provided|Neuronal_ceroid_lipofuscinosis": 2,
    "not_provided|not_specified|Neuronal_ceroid_lipofuscinosis": 2,
    "CTSD-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|CTSD-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_10": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 8,
    "CTSD-related_disorder|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 3,
    "Neuronal_ceroid_lipofuscinosis|not_provided|not_specified|Neuronal_ceroid_lipofuscinosis_10|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|not_specified": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|not_specified": 3,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided": 5,
    "Neuronal_ceroid_lipofuscinosis|CTSD-related_disorder|Neuronal_ceroid_lipofuscinosis_10|Inborn_genetic_diseases|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_10": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_10": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|CTSD-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|not_specified|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_10": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_10": 1,
    "Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_10|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|CTSD-related_disorder|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_10": 1,
    "CTSD-related_disorder|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_10|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_10|not_specified": 2,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive": 2,
    "Distal_arthrogryposis_type_2B1|Arthrogryposis_multiplex_congenita": 2,
    "TNNI2-related_disorder|not_provided": 1,
    "not_specified|Arthrogryposis_multiplex_congenita|not_provided|Arthrogryposis_multiplex_congenita_distal": 1,
    "Distal_arthrogryposis_type_2B1|not_specified|Arthrogryposis_multiplex_congenita|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_distal|Inborn_genetic_diseases|not_provided|Arthrogryposis_multiplex_congenita": 1,
    "Arthrogryposis_multiplex_congenita_distal|Arthrogryposis_multiplex_congenita": 5,
    "not_provided|TNNI2-related_disorder|not_specified|Distal_arthrogryposis_type_2B1": 1,
    "TNNI2-related_disorder": 2,
    "Distal_arthrogryposis_type_2B1|not_specified|not_provided": 1,
    "not_provided|Arthrogryposis_multiplex_congenita_distal|Arthrogryposis_multiplex_congenita": 8,
    "not_specified|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|Distal_arthrogryposis_type_2B1": 6,
    "TNNI2-related_disorder|not_specified|not_provided": 1,
    "not_provided|TNNI2-related_disorder": 1,
    "Distal_arthrogryposis_type_2B1|not_provided|Ulnar_deviation_of_the_wrist|Congenital_finger_flexion_contractures|Calcaneovalgus_deformity|Distal_arthrogryposis": 1,
    "Distal_arthrogryposis_type_2B1|not_provided": 1,
    "TNNI2-related_disorder|not_provided|Distal_arthrogryposis_type_2B1": 1,
    "Distal_arthrogryposis_type_2B1|Arthrogryposis_multiplex_congenita|not_provided": 1,
    "Arthrogryposis_multiplex_congenita|Arthrogryposis_multiplex_congenita_distal": 3,
    "Distal_arthrogryposis_type_2B1|Arthrogryposis_multiplex_congenita_distal": 2,
    "Arthrogryposis|_distal|_type_2B2": 7,
    "Arthrogryposis|_distal|_type_2B2|not_provided": 2,
    "not_provided|TNNT3-related_disorder": 2,
    "TNNT3-related_disorder": 4,
    "not_provided|Arthrogryposis|_distal|_type_2B2|not_specified": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B2": 3,
    "not_provided|TNNT3-related_disorder|Arthrogryposis_multiplex_congenita_distal|Arthrogryposis_multiplex_congenita": 1,
    "Arthyrgryposis|_distal|_type_2B|Arthrogryposis|_distal|_type_2B2|not_provided": 1,
    "Arthrogryposis|_distal|_type_2B2|Arthyrgryposis|_distal|_type_2B|not_provided": 1,
    "not_provided|Arthrogryposis_multiplex_congenita|not_specified|Distal_arthrogryposis_type_2B1": 1,
    "Arthrogryposis_multiplex_congenita_distal|not_specified|not_provided|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|Arthrogryposis_multiplex_congenita|Arthrogryposis_multiplex_congenita_distal": 2,
    "Distal_arthrogryposis_type_2B1|Arthrogryposis_multiplex_congenita_distal|not_provided": 1,
    "TNNT3-related_disorder|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Arthrogryposis_multiplex_congenita_distal|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B2|TNNT3-related_disorder": 1,
    "Arthrogryposis_multiplex_congenita_distal|not_specified|not_provided|Distal_arthrogryposis_type_2B1": 1,
    "not_specified|not_provided|Arthrogryposis|_distal|_type_2B2": 1,
    "not_specified|Arthrogryposis_multiplex_congenita|Arthrogryposis_multiplex_congenita_distal|not_provided": 1,
    "Arthrogryposis_multiplex_congenita_distal|not_provided|not_specified|Distal_arthrogryposis_type_2B1": 1,
    "not_specified|not_provided|Distal_arthrogryposis_type_2B1|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|Arthrogryposis_multiplex_congenita|Distal_arthrogryposis_type_2B1": 1,
    "Arthrogryposis_multiplex_congenita|Distal_arthrogryposis_type_2B1": 1,
    "H19-related_disorder": 41,
    "MIR675-related_disorder": 1,
    "INSULIN-LIKE_GROWTH_FACTOR_II_POLYMORPHISM": 3,
    "IGF2-related_disorder": 6,
    "Wilms_tumor_1|Silver-Russell_syndrome_3|Beckwith-Wiedemann_syndrome|Silver-Russell_syndrome_1": 1,
    "not_provided|IGF2-related_disorder": 2,
    "Silver-Russell_syndrome_3|not_provided": 1,
    "Inborn_genetic_diseases|Silver-Russell_syndrome_3|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Silver-Russell_syndrome_1|Wilms_tumor_1|Beckwith-Wiedemann_syndrome|Silver-Russell_syndrome_3": 1,
    "Silver-Russell_syndrome_3|Inborn_genetic_diseases": 1,
    "IGF2-related_disorder|not_provided": 3,
    "Silver-Russell_syndrome_3": 15,
    "Silver-Russell_syndrome_1": 3,
    "not_provided|Silver-Russell_syndrome_3": 1,
    "Silver-Russell_syndrome_3|Wilms_tumor_1|Beckwith-Wiedemann_syndrome|Silver-Russell_syndrome_1": 1,
    "not_provided|Silver-Russell_syndrome_1": 1,
    "Wilms_tumor_1|Silver-Russell_syndrome_3|Beckwith-Wiedemann_syndrome|Silver-Russell_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Silver-Russell_syndrome_1|Silver-Russell_syndrome_3|Wilms_tumor_1|Beckwith-Wiedemann_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Permanent_neonatal_diabetes_mellitus|Type_1_diabetes_mellitus_2|Hyperproinsulinemia|Maturity-onset_diabetes_of_the_young_type_10|Diabetes_mellitus|_permanent_neonatal_4": 1,
    "INS-related_disorder": 9,
    "Neonatal_insulin-dependent_diabetes_mellitus|Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity-onset_diabetes_of_the_young_type_10": 2,
    "Maturity-onset_diabetes_of_the_young_type_10|Transient_Neonatal_Diabetes|_Dominant/Recessive|Neonatal_insulin-dependent_diabetes_mellitus": 3,
    "Maturity-onset_diabetes_of_the_young_type_10|Type_1_diabetes_mellitus_2|Autosomal_recessive_DOPA_responsive_dystonia|Diabetes_mellitus|_permanent_neonatal_4|Transient_Neonatal_Diabetes|_Dominant/Recessive|Diabetes_mellitus_type_1|not_provided|Hyperproinsulinemia|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Hypoinsulinemia|Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_10|Autosomal_recessive_DOPA_responsive_dystonia|not_specified": 1,
    "Neonatal_diabetes_mellitus": 16,
    "not_specified|Neonatal_insulin-dependent_diabetes_mellitus": 6,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_4": 8,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Diabetes_mellitus|_permanent_neonatal_4": 1,
    "Neonatal_insulin-dependent_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_10": 1,
    "Neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_4|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Type_1_diabetes_mellitus_2|Diabetes_mellitus": 1,
    "Diabetes_mellitus|_permanent_neonatal_4": 3,
    "not_provided|INS-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Monogenic_diabetes": 1,
    "Diabetes_mellitus|_permanent_neonatal_4|Hyperproinsulinemia": 1,
    "Hyperproinsulinemia": 5,
    "Diabetes_mellitus|_permanent_neonatal_4|Hyperproinsulinemia|Type_1_diabetes_mellitus_2|Maturity-onset_diabetes_of_the_young_type_10|INS-related_disorder|not_provided": 1,
    "Neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|not_provided|INS-related_disorder|Diabetes_mellitus|_permanent_neonatal_4": 1,
    "Type_1_diabetes_mellitus_2|Hyperproinsulinemia|Maturity-onset_diabetes_of_the_young_type_10|not_provided|not_specified": 1,
    "INS-related_disorder|not_provided": 2,
    "Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|Hyperproinsulinemia|Maturity-onset_diabetes_of_the_young_type_10|not_provided": 2,
    "Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|Hyperproinsulinemia|Maturity-onset_diabetes_of_the_young_type_10": 8,
    "not_provided|INS-related_disorder|Type_2_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Maturity_onset_diabetes_mellitus_in_young|Neonatal_insulin-dependent_diabetes_mellitus|not_specified|not_provided|Diabetes_mellitus|_permanent_neonatal_4|Type_1_diabetes_mellitus_2|Hyperproinsulinemia|Transient_Neonatal_Diabetes|_Dominant/Recessive": 1,
    "Type_1_diabetes_mellitus_2|Hyperproinsulinemia|Diabetes_mellitus|_permanent_neonatal_4|Maturity-onset_diabetes_of_the_young_type_10|not_specified|Neonatal_diabetes_mellitus|not_provided|Neonatal_insulin-dependent_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Neonatal_insulin-dependent_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_4": 1,
    "Neonatal_insulin-dependent_diabetes_mellitus|not_specified": 3,
    "Neonatal_insulin-dependent_diabetes_mellitus": 4,
    "Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity-onset_diabetes_of_the_young_type_10": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Hyperproinsulinemia|Diabetes_mellitus|_permanent_neonatal_4|Type_1_diabetes_mellitus_2|Transient_Neonatal_Diabetes|_Dominant/Recessive|Autosomal_recessive_DOPA_responsive_dystonia|Type_2_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus|Neonatal_insulin-dependent_diabetes_mellitus": 1,
    "Diabetes_mellitus_type_1|not_provided|INS-related_disorder|Monogenic_diabetes|Type_1_diabetes_mellitus_2": 1,
    "Maturity-onset_diabetes_of_the_young_type_10": 4,
    "Transient_Neonatal_Diabetes|_Dominant/Recessive|not_specified|Maturity-onset_diabetes_of_the_young_type_10": 1,
    "Inborn_genetic_diseases|Neonatal_insulin-dependent_diabetes_mellitus|not_provided": 1,
    "Hyperproinsulinemia|not_provided|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|Neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_4": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_10|Diabetes_mellitus|_permanent_neonatal_4": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Transient_Neonatal_Diabetes|_Dominant/Recessive|not_provided": 1,
    "Diabetes_mellitus|_permanent_neonatal_4|Neonatal_diabetes_mellitus|not_provided|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|not_provided": 1,
    "Diabetes_mellitus|_permanent_neonatal_4|Neonatal_diabetes_mellitus|not_provided|Type_1_diabetes_mellitus_2|Permanent_neonatal_diabetes_mellitus": 1,
    "Neonatal_insulin-dependent_diabetes_mellitus|Inborn_genetic_diseases|not_provided|Maturity-onset_diabetes_of_the_young_type_10|Transient_Neonatal_Diabetes|_Dominant/Recessive": 1,
    "Neonatal_diabetes_mellitus|not_provided": 2,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_4|not_provided": 1,
    "not_specified|not_provided|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_10|INS-IGF2-related_disorder|Diabetes_mellitus|_permanent_neonatal_4|Type_1_diabetes_mellitus_2|Hyperproinsulinemia|Transient_Neonatal_Diabetes|_Dominant/Recessive": 1,
    "Neonatal_insulin-dependent_diabetes_mellitus|Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Inborn_genetic_diseases|Maturity-onset_diabetes_of_the_young_type_10|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Neonatal_insulin-dependent_diabetes_mellitus|Autosomal_recessive_DOPA_responsive_dystonia|Diabetes_mellitus|_permanent_neonatal_4|Hyperproinsulinemia|Type_1_diabetes_mellitus_2|Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_10|Diabetes_mellitus|_permanent_neonatal_4|Type_1_diabetes_mellitus_2|Hyperproinsulinemia": 1,
    "Permanent_neonatal_diabetes_mellitus|Neonatal_insulin-dependent_diabetes_mellitus": 1,
    "Neonatal_insulin-dependent_diabetes_mellitus|INS-related_disorder|Maturity-onset_diabetes_of_the_young_type_10|Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|Hyperproinsulinemia|Transient_Neonatal_Diabetes|_Dominant/Recessive": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|not_provided|Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|INS-related_disorder|Hyperproinsulinemia": 1,
    "INS-IGF2-related_disorder|not_provided": 1,
    "not_provided|Diabetes_mellitus|_permanent_neonatal_4|Maturity-onset_diabetes_of_the_young_type_10|Hyperproinsulinemia|Type_1_diabetes_mellitus_2": 1,
    "Neonatal_diabetes_mellitus|not_specified|Diabetes_mellitus|_permanent_neonatal_4|Autosomal_recessive_DOPA_responsive_dystonia|Maturity-onset_diabetes_of_the_young_type_10|not_provided|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Dominant/Recessive": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Autosomal_recessive_DOPA_responsive_dystonia|Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Transient_Neonatal_Diabetes|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young|Autosomal_recessive_DOPA_responsive_dystonia|not_provided": 1,
    "Neonatal_insulin-dependent_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus": 1,
    "not_specified|INS-related_disorder|not_provided|Type_2_diabetes_mellitus": 1,
    "not_specified|Neonatal_insulin-dependent_diabetes_mellitus|not_provided": 1,
    "Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|Maturity-onset_diabetes_of_the_young_type_10|Hyperproinsulinemia|INS-related_disorder|not_provided": 1,
    "Diabetes_mellitus|not_specified|Type_1_diabetes_mellitus_2|Maturity-onset_diabetes_of_the_young_type_10|Hyperproinsulinemia|Diabetes_mellitus|_permanent_neonatal_4|Amyotrophic_lateral_sclerosis|_susceptibility_to|_24|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "Hyperproinsulinemia|Maturity-onset_diabetes_of_the_young_type_10|Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|Permanent_neonatal_diabetes_mellitus|INS-related_disorder|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_10|Hyperproinsulinemia|Type_1_diabetes_mellitus_2|Diabetes_mellitus|_permanent_neonatal_4|not_specified|not_provided": 1,
    "Autosomal_recessive_DOPA_responsive_dystonia|Neonatal_insulin-dependent_diabetes_mellitus|Transient_Neonatal_Diabetes|_Dominant/Recessive|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Autosomal_recessive_DOPA_responsive_dystonia": 939,
    "Autosomal_recessive_DOPA_responsive_dystonia|Inborn_genetic_diseases": 21,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_DOPA_responsive_dystonia": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_DOPA_responsive_dystonia": 14,
    "Autosomal_recessive_DOPA_responsive_dystonia|not_specified": 4,
    "Autosomal_recessive_DOPA_responsive_dystonia|Transient_Neonatal_Diabetes|_Dominant/Recessive|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Autosomal_recessive_DOPA_responsive_dystonia": 50,
    "not_specified|not_provided|TH-related_disorder|Autosomal_recessive_DOPA_responsive_dystonia": 1,
    "TH-related_disorder|not_provided|Autosomal_recessive_DOPA_responsive_dystonia": 2,
    "Autosomal_recessive_DOPA_responsive_dystonia|not_provided": 17,
    "TH-related_disorder|Autosomal_recessive_DOPA_responsive_dystonia": 2,
    "Autosomal_recessive_DOPA_responsive_dystonia|not_provided|not_specified": 2,
    "Neonatal_insulin-dependent_diabetes_mellitus|Autosomal_recessive_DOPA_responsive_dystonia|Transient_Neonatal_Diabetes|_Dominant/Recessive|not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "not_provided|Autosomal_recessive_DOPA_responsive_dystonia|TH-related_disorder": 1,
    "not_specified|not_provided|Autosomal_recessive_DOPA_responsive_dystonia": 7,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Transient_Neonatal_Diabetes|_Dominant/Recessive|Autosomal_recessive_DOPA_responsive_dystonia|Generalized_dystonia|not_specified": 1,
    "not_specified|Autosomal_recessive_DOPA_responsive_dystonia": 4,
    "not_provided|Autosomal_recessive_DOPA_responsive_dystonia|not_specified": 6,
    "Autosomal_recessive_DOPA_responsive_dystonia|Inborn_genetic_diseases|not_provided": 2,
    "TH-related_disorder": 2,
    "not_provided|Autosomal_recessive_DOPA_responsive_dystonia|Inborn_genetic_diseases": 6,
    "not_specified|Autosomal_recessive_DOPA_responsive_dystonia|not_provided": 1,
    "Autosomal_recessive_DOPA_responsive_dystonia|Dystonic_disorder": 2,
    "Autosomal_recessive_DOPA_responsive_dystonia|TH-related_disorder": 5,
    "not_provided|not_specified|Autosomal_recessive_DOPA_responsive_dystonia": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_DOPA_responsive_dystonia|not_provided": 3,
    "Autosomal_recessive_DOPA_responsive_dystonia|not_provided|Dystonia_5": 1,
    "Autosomal_recessive_DOPA_responsive_dystonia|not_provided|Inborn_genetic_diseases": 4,
    "Autosomal_recessive_DOPA_responsive_dystonia|TH-related_disorder|not_provided": 2,
    "not_provided|TH-related_disorder|Autosomal_recessive_DOPA_responsive_dystonia": 1,
    "Autosomal_recessive_DOPA_responsive_dystonia|not_specified|not_provided": 1,
    "TH-related_disorder|not_provided|not_specified|Autosomal_recessive_DOPA_responsive_dystonia": 1,
    "TH-related_disorder|Autosomal_recessive_DOPA_responsive_dystonia|not_provided": 1,
    "not_specified|Autosomal_recessive_DOPA_responsive_dystonia|Schizophrenia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_DOPA_responsive_dystonia": 1,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided|Autosomal_recessive_DOPA_responsive_dystonia": 1,
    "not_provided|TH-related_disorder|Autosomal_recessive_DOPA_responsive_dystonia|not_specified": 1,
    "Autosomal_recessive_DOPA_responsive_dystonia|Schizophrenia": 1,
    "not_provided|CD81-related_disorder": 4,
    "not_specified|Immunodeficiency|_common_variable|_6|not_provided": 1,
    "Immunodeficiency|_common_variable|_6|not_provided": 4,
    "CD81-related_disorder|not_provided": 2,
    "Immunodeficiency|_common_variable|_6": 2,
    "not_provided|Immunodeficiency|_common_variable|_6|not_specified": 1,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_6": 1,
    "not_provided|Immunodeficiency|_common_variable|_6": 1,
    "not_provided|not_specified|Immunodeficiency|_common_variable|_6": 1,
    "CD81-related_disorder": 1,
    "Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Congenital_long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1": 16,
    "Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Short_QT_syndrome|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation|Congenital_long_QT_syndrome": 4,
    "not_provided|Long_QT_syndrome|Short_QT_syndrome_type_2|Cardiovascular_phenotype|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome": 1,
    "Conduction_disorder_of_the_heart|Long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|not_specified|not_provided": 1,
    "Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|not_specified|Ventricular_fibrillation|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|KCNQ1-related_disorder": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 6,
    "Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Cardiovascular_phenotype|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 2,
    "Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome|KCNQ1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Short_QT_syndrome_type_2|Long_QT_syndrome_1|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3": 1,
    "Long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|KCNQ1-related_disorder|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 3,
    "Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Beckwith-Wiedemann_syndrome|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_1": 2,
    "not_provided|Long_QT_syndrome_1|Long_QT_syndrome": 2,
    "Long_QT_syndrome|KCNQ1-related_disorder|not_provided|Long_QT_syndrome_1|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Long_QT_syndrome|not_provided|Short_QT_syndrome_type_2": 1,
    "not_specified|KCNQ1-related_disorder|not_provided": 1,
    "Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|not_specified": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|not_provided|Long_QT_syndrome": 3,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Atrial_fibrillation|Atrial_fibrillation|_familial|_3": 1,
    "Long_QT_syndrome|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Atrial_fibrillation|Short_QT_syndrome_type_2|Long_QT_syndrome|not_provided|KCNQ1-related_disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_1|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided": 1,
    "not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 5,
    "Atrial_fibrillation|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1|Hearing_impairment": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified|Long_QT_syndrome|Long_QT_syndrome_1|Hypertrophic_cardiomyopathy": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|not_specified|not_provided|Short_QT_syndrome_type_2|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_1|not_provided|not_specified|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Jervell_and_Lange-Nielsen_syndrome|not_specified|Cardiac_arrhythmia|Short_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Familial_atrial_fibrillation": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Congenital_long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome_1|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Rare_genetic_deafness|Congenital_long_QT_syndrome|KCNQ1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|not_provided|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Congenital_long_QT_syndrome": 2,
    "Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome|not_provided|Beckwith-Wiedemann_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "KCNQ1-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome": 1,
    "Recurrent_spontaneous_abortion|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|not_provided": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_1": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "KCNQ1-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1|Congenital_long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1/2|_digenic": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_1|KCNQ1-related_disorder|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_1|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_1|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|KCNQ1-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Long_QT_syndrome|not_specified|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Atrial_fibrillation": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|KCNQ1-related_disorder|not_specified": 1,
    "Autosomal_dominant_KCNQ1-related_disease|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 2,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1": 2,
    "Long_QT_syndrome_1|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_1": 1,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_1|Long_QT_syndrome|KCNQ1-related_disorder|Congenital_long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome|not_provided|KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome|Atrial_fibrillation|_familial|_3|Atrial_fibrillation": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "not_provided|not_specified|KCNQ1-related_disorder|Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_1|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|Short_QT_syndrome|Long_QT_syndrome|Familial_atrial_fibrillation": 2,
    "Torsades_de_pointes|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|not_specified|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome": 4,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|not_specified|not_provided|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 6,
    "KCNQ1-related_disorder|Long_QT_syndrome|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 4,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiac_arrhythmia": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|not_provided|Long_QT_syndrome_1|Short_QT_syndrome_type_2|not_specified|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|Long_QT_syndrome_1|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia|Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|KCNQ1-related_disorder|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1/2|_digenic|Congenital_long_QT_syndrome": 1,
    "Abnormality_of_the_cardiovascular_system|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 2,
    "Long_QT_syndrome_1|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided": 2,
    "Cardiac_arrhythmia|Long_QT_syndrome_1": 2,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome|Short_QT_syndrome_type_2|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Monogenic_hearing_loss|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|Short_QT_syndrome_type_2|KCNQ1-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|KCNQ1-related_disorder": 1,
    "Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Familial_atrial_fibrillation|Long_QT_syndrome|Short_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_1|Long_QT_syndrome|Prolonged_QT_interval": 1,
    "not_provided|Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2": 1,
    "Cardiac_arrhythmia|not_provided|Short_QT_syndrome_type_2": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified": 3,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|not_specified|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_1|KCNQ1-related_disorder|not_provided|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Long_QT_syndrome|Long_QT_syndrome_1|not_provided": 3,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|KCNQ1-related_disorder|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Cardiac_arrhythmia": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Short_QT_syndrome_type_2": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 2,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|not_specified|not_provided": 1,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|not_specified|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "KCNQ1-related_disorder|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome_1|not_provided|Congenital_long_QT_syndrome": 1,
    "Short_QT_syndrome|Long_QT_syndrome|Short_QT_syndrome_type_2": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1|Long_QT_syndrome": 2,
    "Long_QT_syndrome_1|Congenital_long_QT_syndrome|Cardiac_arrhythmia|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_1|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1|Long_QT_syndrome|not_provided": 1,
    "not_specified|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|not_specified|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1|Congenital_long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_1": 1,
    "not_provided|Long_QT_syndrome_1|Long_QT_syndrome|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_1/2|_digenic|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_1|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_2|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_specified|not_provided": 1,
    "Cardiac_arrhythmia|not_provided|not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome_1|Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Paroxysmal_atrial_fibrillation|Long_QT_syndrome_1|KCNQ1-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "KCNQ1-related_disorder|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|KCNQ1-related_disorder": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|KCNQ1-related_disorder|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|Beckwith-Wiedemann_syndrome|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "not_provided|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|KCNQ1-related_disorder|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia|Beckwith-Wiedemann_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 3,
    "Long_QT_syndrome_1|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Hearing_impairment|Cardiovascular_phenotype|Cardiac_arrhythmia|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_specified": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_1|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|not_provided|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|not_specified|Cardiomyopathy|Long_QT_syndrome|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Familial_atrial_fibrillation|not_specified|not_provided|Long_QT_syndrome|Wolff-Parkinson-White_pattern": 1,
    "Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia": 2,
    "Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|Long_QT_syndrome|not_provided|Short_QT_syndrome_type_2|not_specified|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_1|not_provided": 1,
    "not_specified|Congenital_long_QT_syndrome|Short_QT_syndrome|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|not_provided|Familial_atrial_fibrillation": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome|Ear_malformation": 1,
    "not_specified|Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiac_arrhythmia|Beckwith-Wiedemann_syndrome|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome|KCNQ1-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_1|Cardiac_arrhythmia": 1,
    "Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Short_QT_syndrome_type_2|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|not_provided": 1,
    "Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Beckwith-Wiedemann_syndrome|Long_QT_syndrome|not_provided": 1,
    "Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|not_specified|Familial_atrial_fibrillation|Long_QT_syndrome|Short_QT_syndrome|Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "not_provided|KCNQ1-related_disorder": 24,
    "Familial_atrial_fibrillation|Congenital_long_QT_syndrome|Short_QT_syndrome|Long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|not_provided|Familial_atrial_fibrillation|Short_QT_syndrome|Long_QT_syndrome": 1,
    "KCNQ1-related_disorder|not_provided": 24,
    "KCNQ1-related_disorder": 91,
    "Congenital_long_QT_syndrome|Short_QT_syndrome|Long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation": 1,
    "Long_QT_syndrome|Short_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation|Congenital_long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Short_QT_syndrome|not_provided|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation": 1,
    "KCNQ1OT1-related_disorder": 2,
    "Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|not_specified": 1,
    "Atrial_fibrillation|_familial|_3|Cardiac_arrhythmia|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|Long_QT_syndrome|not_provided|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Sudden_cardiac_death": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_provided|Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Atrial_fibrillation|_familial|_3|not_provided": 1,
    "not_specified|Long_QT_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|KCNQ1-related_disorder": 1,
    "Long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|not_provided|not_specified|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Cardiac_arrhythmia|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "KCNQ1-related_epilepsy|Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Short_QT_syndrome|not_specified|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation": 1,
    "not_specified|not_provided|KCNQ1-related_disorder|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_specified|KCNQ1-related_disorder": 1,
    "Autosomal_dominant_KCNQ1-related_disease": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Short_QT_syndrome|Familial_atrial_fibrillation|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Beckwith-Wiedemann_syndrome|Silver-Russell_syndrome_1": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1|Cardiac_arrhythmia|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|KCNQ1-related_disorder|Monogenic_hearing_loss|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Long_QT_syndrome|Long_QT_syndrome_1|_recessive": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|not_specified|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|not_specified|Long_QT_syndrome|not_provided": 1,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Long_QT_syndrome|KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1|_recessive|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_1|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|KCNQ1-related_disorder|Cardiovascular_phenotype|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Short_QT_syndrome_type_2|Long_QT_syndrome_1|not_specified|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|not_specified|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|not_provided": 1,
    "not_provided|not_specified|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|KCNQ1-related_disorder|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_1": 1,
    "not_specified|Congenital_long_QT_syndrome|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_1|not_specified|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1|not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1|not_provided": 1,
    "Congenital_long_QT_syndrome|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 2,
    "Long_QT_syndrome|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2": 1,
    "Jervell_and_Lange-Nielsen_syndrome": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Long_QT_syndrome_1": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_3|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|not_specified": 1,
    "Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|not_specified": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "not_specified|Cardiac_arrhythmia|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome_1|not_provided|Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Beckwith-Wiedemann_syndrome|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Acquired_susceptibility_to_long_QT_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Familial_atrial_fibrillation|Short_QT_syndrome|Cardiac_arrhythmia|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome|not_provided|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome|not_provided|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Beckwith-Wiedemann_syndrome|not_provided|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|not_specified|Long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Congenital_long_QT_syndrome": 2,
    "Long_QT_syndrome|Cardiac_arrhythmia|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "not_specified|KCNQ1-related_disorder|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome|KCNQ1-related_disorder|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "KCNQ1-related_disorder|Cardiac_arrhythmia|Congenital_long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|Cardiac_arrhythmia|not_provided|Long_QT_syndrome": 1,
    "KCNQ1-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2": 1,
    "Cardiac_arrhythmia|KCNQ1-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|KCNQ1-related_disorder|not_specified|not_provided|Long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Cardiac_arrhythmia|Long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Cardiac_arrhythmia": 1,
    "Cardiac_arrhythmia|not_specified|KCNQ1-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|not_provided": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1|not_provided|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome_1|not_specified|not_provided|Long_QT_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Brugada_syndrome|Cardiac_arrhythmia|Cardiovascular_phenotype": 1,
    "not_provided|Cardiac_arrhythmia|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|not_provided|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|KCNQ1-related_disorder|Cardiac_arrhythmia|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "not_provided|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|not_specified|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Polymorphic_ventricular_tachycardia|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Beckwith-Wiedemann_syndrome|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Cardiac_arrhythmia|Long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|Long_QT_syndrome_1": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome|not_specified|Long_QT_syndrome_1|Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided": 1,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|Atrial_fibrillation|_familial|_3|Beckwith-Wiedemann_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Cardiac_arrhythmia|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Cardiac_arrhythmia|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|Long_QT_syndrome|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation|Short_QT_syndrome|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Cardiac_arrhythmia|Long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Cardiac_arrhythmia|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 1,
    "Cardiac_arrhythmia|KCNQ1-related_disorder": 1,
    "Familial_atrial_fibrillation|Short_QT_syndrome|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3": 4,
    "Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1": 3,
    "Congenital_long_QT_syndrome|Short_QT_syndrome|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation": 1,
    "Congenital_long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome|Short_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation|Congenital_long_QT_syndrome": 1,
    "not_provided|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome": 2,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Short_QT_syndrome|Long_QT_syndrome|Familial_atrial_fibrillation|Congenital_long_QT_syndrome": 2,
    "not_provided|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Congenital_long_QT_syndrome": 1,
    "not_provided|Short_QT_syndrome|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation": 1,
    "Congenital_long_QT_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Congenital_long_QT_syndrome": 3,
    "Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome|Short_QT_syndrome|Familial_atrial_fibrillation": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Congenital_long_QT_syndrome|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Congenital_long_QT_syndrome": 1,
    "Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3|Congenital_long_QT_syndrome": 4,
    "Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3": 1,
    "Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Short_QT_syndrome_type_2|Long_QT_syndrome_1|Jervell_and_Lange-Nielsen_syndrome_1|not_provided": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Congenital_long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_1|not_provided|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Long_QT_syndrome_1|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Short_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome|Familial_atrial_fibrillation": 1,
    "not_provided|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_3|Long_QT_syndrome": 1,
    "not_provided|Short_QT_syndrome_type_2|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Atrial_fibrillation|_familial|_3": 1,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_1|Long_QT_syndrome_1|Short_QT_syndrome_type_2|Atrial_fibrillation|_familial|_3": 1,
    "CDKN1C-related_disorder": 10,
    "not_provided|Beckwith-Wiedemann_syndrome|IMAGe_syndrome|CDKN1C-related_disorder": 1,
    "Beckwith-Wiedemann_syndrome|IMAGe_syndrome": 47,
    "IMAGe_syndrome|Beckwith-Wiedemann_syndrome|not_provided": 2,
    "Beckwith-Wiedemann_syndrome|not_provided": 12,
    "Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome": 5,
    "Beckwith-Wiedemann_syndrome|not_specified": 4,
    "not_provided|Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder": 3,
    "Beckwith-Wiedemann_syndrome|Inborn_genetic_diseases|IMAGe_syndrome": 5,
    "not_provided|Beckwith-Wiedemann_syndrome|IMAGe_syndrome": 4,
    "Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder": 10,
    "IMAGe_syndrome": 8,
    "IMAGe_syndrome|Silver-Russell_syndrome_1|Beckwith-Wiedemann_syndrome": 1,
    "IMAGe_syndrome|not_provided": 2,
    "Beckwith-Wiedemann_syndrome|Inborn_genetic_diseases": 13,
    "CDKN1C-related_disorder|Beckwith-Wiedemann_syndrome": 7,
    "Inborn_genetic_diseases|IMAGe_syndrome|Beckwith-Wiedemann_syndrome": 2,
    "IMAGe_syndrome|Beckwith-Wiedemann_syndrome": 25,
    "Beckwith-Wiedemann_syndrome|IMAGe_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Beckwith-Wiedemann_syndrome|IMAGe_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Beckwith-Wiedemann_syndrome|IMAGe_syndrome": 1,
    "Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome|IMAGe_syndrome": 2,
    "Beckwith-Wiedemann_syndrome|not_specified|not_provided": 1,
    "Beckwith-Wiedemann_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Beckwith-Wiedemann_syndrome|not_provided|not_specified|CDKN1C-related_disorder|IMAGe_syndrome": 1,
    "CDKN1C-related_disorder|not_provided|Beckwith-Wiedemann_syndrome": 4,
    "CDKN1C-related_disorder|Beckwith-Wiedemann_syndrome|IMAGe_syndrome": 2,
    "not_specified|not_provided|Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder": 1,
    "not_specified|not_provided|Beckwith-Wiedemann_syndrome|IMAGe_syndrome": 1,
    "not_specified|not_provided|Beckwith-Wiedemann_syndrome": 5,
    "CDKN1C-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "CDKN1C-related_disorder|not_provided|Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome": 1,
    "Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder|not_specified": 1,
    "Beckwith-Wiedemann_syndrome|not_specified|not_provided|IMAGe_syndrome": 1,
    "not_specified|Beckwith-Wiedemann_syndrome": 2,
    "Beckwith-Wiedemann_syndrome|IMAGe_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome|not_provided|IMAGe_syndrome": 1,
    "Inborn_genetic_diseases|CDKN1C-related_disorder|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "Hereditary_cancer|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "Beckwith-Wiedemann_syndrome|not_provided|not_specified|CDKN1C-related_disorder|Inborn_genetic_diseases": 1,
    "CDKN1C-related_disorder|Beckwith-Wiedemann_syndrome|not_specified|not_provided": 1,
    "CDKN1C-related_disorder|not_specified|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "CDKN1C-related_disorder|Beckwith-Wiedemann_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder|IMAGe_syndrome": 2,
    "not_provided|Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome|IMAGe_syndrome|not_provided": 1,
    "Beckwith-Wiedemann_syndrome|IMAGe_syndrome|Inborn_genetic_diseases": 4,
    "Beckwith-Wiedemann_syndrome|not_provided|IMAGe_syndrome": 1,
    "Beckwith-Wiedemann_syndrome|IMAGe_syndrome|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome": 1,
    "Beckwith-Wiedemann_syndrome_due_to_CDKN1C_mutation|IMAGe_syndrome|Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder|not_provided": 1,
    "not_provided|IMAGe_syndrome|Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder": 1,
    "not_provided|IMAGe_syndrome|Beckwith-Wiedemann_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|IMAGe_syndrome|Beckwith-Wiedemann_syndrome": 1,
    "not_provided|not_specified|Beckwith-Wiedemann_syndrome": 2,
    "Beckwith-Wiedemann_syndrome|CDKN1C-related_disorder|Inborn_genetic_diseases|IMAGe_syndrome": 1,
    "IMAGe_syndrome|not_provided|Beckwith-Wiedemann_syndrome": 1,
    "SLC22A18-related_disorder|Rhabdomyosarcoma|_somatic": 1,
    "SLC22A18-related_disorder": 2,
    "not_specified|Microcephaly|_developmental_delay|_and_brittle_hair_syndrome": 2,
    "Microcephaly|_developmental_delay|_and_brittle_hair_syndrome": 11,
    "CARS1-related_disorder": 5,
    "Microcephaly|_developmental_delay|_and_brittle_hair_syndrome|not_provided|not_specified": 1,
    "Microcephaly|_developmental_delay|_and_brittle_hair_syndrome|not_specified|not_provided": 1,
    "Microcephaly|_developmental_delay|_and_brittle_hair_syndrome|not_specified": 1,
    "OSBPL5-related_disorder": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_3": 19,
    "Inborn_genetic_diseases|not_provided|Congenital_omphalocele|Hypoplasia_of_the_corpus_callosum|Micrognathia": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_3|Inborn_genetic_diseases": 2,
    "PGAP2-related_disorder": 2,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_3|not_provided": 1,
    "Genetic_developmental_and_epileptic_encephalopathy": 9,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_3": 2,
    "Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_3": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_3|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_3": 1,
    "Inborn_genetic_diseases|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_3": 1,
    "RHOG-related_condition": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome": 127,
    "not_provided|not_specified|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "not_provided|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome": 2,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 68,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome": 106,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided|Immunodeficiency|_common_variable|_10": 1,
    "Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 98,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 75,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates": 80,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome|not_specified": 2,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Inborn_genetic_diseases": 3,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_specified": 1,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided": 3,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|not_specified": 1,
    "Inborn_genetic_diseases|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates": 6,
    "not_specified|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 2,
    "not_provided|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 5,
    "not_specified|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Inborn_genetic_diseases": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Inborn_genetic_diseases": 4,
    "Myopathy|_autophagic_vacuolar|_infantile-onset": 1,
    "Myopathy|_tubular_aggregate|_1": 9,
    "Combined_immunodeficiency_due_to_STIM1_deficiency": 9,
    "STIM1-related_disorder|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome": 4,
    "Myopathy|_tubular_aggregate|_1|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 2,
    "Stormorken_syndrome": 3,
    "Myopathy|_tubular_aggregate|_1|Myopathy_with_tubular_aggregates": 1,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|not_provided": 4,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|STIM1-related_disorder|not_provided": 1,
    "Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided|Myopathy|_tubular_aggregate|_1": 2,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Myopathy|_tubular_aggregate|_1|Inborn_genetic_diseases": 1,
    "not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Myopathy|_tubular_aggregate|_1": 1,
    "not_provided|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_specified": 3,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|not_specified": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy|_tubular_aggregate|_1|Stormorken_syndrome|Myopathy_with_tubular_aggregates|not_provided": 1,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "not_specified|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy|_tubular_aggregate|_1|not_provided|Myopathy_with_tubular_aggregates": 1,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Myopathy|_tubular_aggregate|_1|not_provided": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy|_tubular_aggregate|_1|Myopathy_with_tubular_aggregates": 1,
    "not_provided|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates": 6,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|STIM1-related_disorder": 2,
    "Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|STIM1-related_disorder": 1,
    "not_provided|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|STIM1-related_disorder": 2,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 5,
    "STIM1-related_disorder|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome": 1,
    "Inborn_genetic_diseases|Myopathy|_tubular_aggregate|_1|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|STIM1-related_disorder|Myopathy_with_tubular_aggregates": 1,
    "not_provided|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy|_tubular_aggregate|_1": 1,
    "not_provided|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 2,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Myopathy|_tubular_aggregate|_1": 1,
    "not_provided|STIM1-related_disorder|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome": 1,
    "Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy|_tubular_aggregate|_1": 2,
    "STIM1-related_disorder": 7,
    "not_provided|STIM1-related_disorder|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|not_specified|not_provided": 1,
    "STIM1-related_disorder|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates": 1,
    "Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided": 4,
    "not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome": 4,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Inborn_genetic_diseases": 2,
    "not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Inborn_genetic_diseases": 2,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided|Myopathy_with_tubular_aggregates": 1,
    "Inborn_genetic_diseases|not_specified|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|not_provided": 4,
    "not_specified|not_provided|Stormorken_syndrome|Myopathy|_tubular_aggregate|_1|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates": 1,
    "Myopathy|_tubular_aggregate|_1|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "Stormorken_syndrome|Myopathy|_tubular_aggregate|_1|not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|not_specified": 1,
    "not_specified|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome": 1,
    "not_specified|not_provided|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "not_specified|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 1,
    "Myopathy|_tubular_aggregate|_1|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy|_tubular_aggregate|_1|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 1,
    "Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|not_provided|Inborn_genetic_diseases": 2,
    "Stormorken_syndrome|not_provided|Myopathy|_tubular_aggregate|_1|not_specified|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|not_specified|STIM1-related_disorder": 1,
    "Inborn_genetic_diseases|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "not_specified|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 1,
    "Migraine": 1,
    "STIM1-related_disorder|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "Myopathy|_tubular_aggregate|_1|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 2,
    "Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy|_tubular_aggregate|_1|not_provided|STIM1-related_disorder": 1,
    "STIM1-related_disorder|not_provided": 1,
    "not_provided|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy|_tubular_aggregate|_1|STIM1-related_disorder": 1,
    "STIM1-related_disorder|not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Myopathy|_tubular_aggregate|_1": 1,
    "STIM1-related_disorder|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy|_tubular_aggregate|_1|not_provided": 1,
    "Inborn_genetic_diseases|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|not_provided": 1,
    "not_provided|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|not_provided": 1,
    "Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency|Inborn_genetic_diseases": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome|STIM1-related_disorder": 1,
    "not_specified|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Inborn_genetic_diseases|Myopathy|_tubular_aggregate|_1": 1,
    "STIM1-related_disorder|Inborn_genetic_diseases|Stormorken_syndrome|Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency": 1,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Combined_immunodeficiency_due_to_STIM1_deficiency": 2,
    "Stormorken_syndrome|not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates|not_provided": 1,
    "Combined_immunodeficiency_due_to_STIM1_deficiency|Myopathy_with_tubular_aggregates|Stormorken_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Combined_immunodeficiency_due_to_STIM1_deficiency|Stormorken_syndrome|Myopathy_with_tubular_aggregates": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions|_autosomal_recessive_6": 1,
    "RRM1-related_disorder|Progressive_external_ophthalmoplegia_with_mitochondrial_dna_deletions|_autosomal_recessive_6": 1,
    "Hearing_loss|_autosomal_recessive_115": 3,
    "OR52M1-related_disorder": 8,
    "beta_Thalassemia": 140,
    "Beta-thalassemia_major|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|beta_Thalassemia": 12,
    "Erythrocytosis|_familial|_6|Thalassemia": 1,
    "Beta-thalassemia_HBB/LCRB": 13,
    "not_specified|Malaria|_susceptibility_to|Heinz_body_anemia|METHEMOGLOBINEMIA|_BETA_TYPE|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|not_provided": 1,
    "Heinz_body_anemia|METHEMOGLOBINEMIA|_BETA_TYPE|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|Hb_SS_disease": 5,
    "Hb_SS_disease|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|Heinz_body_anemia|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|not_provided": 1,
    "Beta-plus-thalassemia": 4,
    "not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "Beta-plus-thalassemia|beta_Thalassemia|not_provided|Beta-thalassemia_HBB/LCRB": 1,
    "beta_Thalassemia|Beta-plus-thalassemia": 1,
    "not_provided|beta_Thalassemia": 33,
    "Beta-thalassemia_HBB/LCRB|Hemoglobinopathy|beta_Thalassemia|Beta-plus-thalassemia|not_provided": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "Beta-thalassemia_HBB/LCRB|not_specified|not_provided": 1,
    "not_provided|beta_Thalassemia|HBB-related_disorder": 1,
    "Heinz_body_anemia|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|alpha_Thalassemia|Malaria|_susceptibility_to|not_specified|not_provided": 2,
    "Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|Hemoglobin_E|Hb_SS_disease": 2,
    "Hb_SS_disease|beta_Thalassemia|Hemoglobin_E|Fetal_hemoglobin_quantitative_trait_locus_1": 1,
    "not_specified|Hb_SS_disease|beta_Thalassemia|Hemoglobin_E|Fetal_hemoglobin_quantitative_trait_locus_1": 1,
    "not_provided|beta_Thalassemia|Beta_thalassemia_intermedia": 1,
    "Beta-thalassemia_HBB/LCRB|HEMOGLOBIN_TAK|Hemoglobinopathy|not_provided": 1,
    "HEMOGLOBIN_KODAIRA_II": 1,
    "HEMOGLOBIN_KODAIRA": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_COWTOWN": 1,
    "HEMOGLOBIN_COCHIN-PORT_ROYAL": 1,
    "Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|HEMOGLOBIN_YORK": 1,
    "HEMOGLOBIN_BOLOGNA-ST._ORSOLA": 1,
    "HEMOGLOBIN_HIROSHIMA|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_MCKEES_ROCKS|Erythrocytosis|_familial|_6": 1,
    "not_provided|Erythrocytosis|_familial|_6|HEMOGLOBIN_RAINIER": 1,
    "HEMOGLOBIN_CRANSTON": 1,
    "Erythrocytosis|_familial|_6|not_provided|HEMOGLOBIN_BETHESDA": 1,
    "Erythrocytosis|_familial|_6|Hemoglobinopathy|Dominant_beta-thalassemia|Heinz_body_anemia|Malaria|_susceptibility_to|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB": 1,
    "Erythrocytosis|_familial|_6|not_provided|HEMOGLOBIN_ANDREW-MINNEAPOLIS": 1,
    "HEMOGLOBIN_TRENTO": 1,
    "HEMOGLOBIN_BARBIZON": 1,
    "HEMOGLOBIN_BIRMINGHAM": 1,
    "HEMOGLOBIN_MITO": 1,
    "not_provided|Inborn_genetic_diseases|beta_Thalassemia|not_specified": 1,
    "Erythrocytosis|_familial|_6": 2,
    "HEMOGLOBIN_SAVERNE": 1,
    "HEMOGLOBIN_ABRUZZO|not_provided": 1,
    "Erythrocytosis|_familial|_6|not_specified|HEMOGLOBIN_SYRACUSE": 1,
    "HEMOGLOBIN_RANCHO_MIRAGE": 1,
    "Erythrocytosis|_familial|_6|not_provided|HEMOGLOBIN_OHIO": 1,
    "HEMOGLOBIN_TOYOAKE": 1,
    "HEMOGLOBIN_COVENTRY": 1,
    "not_provided|HEMOGLOBIN_OLMSTED": 1,
    "Hemoglobinopathy|HEMOGLOBIN_PUTTELANGE": 1,
    "not_specified|HEMOGLOBIN_HIMEJI|beta_Thalassemia": 1,
    "HEMOGLOBIN_SAINT_JACQUES|Erythrocytosis|_familial|_6": 1,
    "not_provided|HEMOGLOBIN_HINSDALE": 1,
    "HEMOGLOBIN_SAGAMI|not_provided": 1,
    "HEMOGLOBIN_AURORA": 1,
    "HEMOGLOBIN_GEELONG|HEMOGLOBIN_JINAN": 1,
    "not_provided|HEMOGLOBIN_NIJKERK": 1,
    "HEMOGLOBIN_BROCKTON": 1,
    "HEMOGLOBIN_BUZEN": 1,
    "Beta-thalassemia_HBB/LCRB|Inborn_genetic_diseases|not_specified|not_provided|beta_Thalassemia|Hb_SS_disease": 1,
    "HEMOGLOBIN_'T_LANGE_LAND": 1,
    "HEMOGLOBIN_BECKMAN": 1,
    "HEMOGLOBIN_ALTDORF": 1,
    "Dominant_beta-thalassemia": 2,
    "not_specified|not_provided|beta_Thalassemia|HEMOGLOBIN_YAOUNDE": 1,
    "Hemoglobinopathy": 10,
    "HBB-related_disorder|Inborn_genetic_diseases|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|Hb_SS_disease|beta_Thalassemia|Hemoglobin_E": 1,
    "Inborn_genetic_diseases|Dominant_beta-thalassemia|Heinz_body_anemia|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|alpha_Thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|not_provided": 1,
    "HEMOGLOBIN_RENERT": 1,
    "not_specified|beta_Thalassemia|Dominant_beta-thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia": 1,
    "HEMOGLOBIN_EXTREMADURA": 1,
    "HEMOGLOBIN_YAMAGATA": 1,
    "HEMOGLOBIN_K_(WOOLWICH)|not_provided|not_specified": 1,
    "HEMOGLOBIN_SILVER_SPRINGS": 1,
    "HEMOGLOBIN_SARREBOURG": 1,
    "HEMOGLOBIN_SHANGHAI": 1,
    "HEMOGLOBIN_MOTOWN|HEMOGLOBIN_TOKUCHI|HEMOGLOBIN_CAMDEN|not_specified|not_provided": 1,
    "not_specified|not_provided|HEMOGLOBIN_LESLIE|HEMOGLOBIN_DEACONESS|HEMOGLOBIN_SHELBY": 1,
    "HEMOGLOBIN_NEVERS": 1,
    "HEMOGLOBIN_WIEN": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Hemoglobinopathy|not_provided|HEMOGLOBIN_LA_DESIRADE": 1,
    "HEMOGLOBIN_K_(CAMEROON)|HEMOGLOBIN_J_(TAICHUNG)": 1,
    "not_specified|not_provided|HEMOGLOBIN_CRETE|beta_Thalassemia": 1,
    "beta_Thalassemia|not_provided": 20,
    "not_specified|HEMOGLOBIN_SITIA": 1,
    "HEMOGLOBIN_J_(GUANTANAMO)": 1,
    "HEMOGLOBIN_MONT_SAINT-AIGNAN": 1,
    "not_specified|Delta-beta-thalassemia": 1,
    "beta_Thalassemia|HEMOGLOBIN_DIEPPE": 1,
    "not_specified|.|Beta-plus-thalassemia|_dominant": 1,
    "not_provided|Dominant_beta-thalassemia": 1,
    "HEMOGLOBIN_HACETTEPE|HEMOGLOBIN_COMPLUTENSE": 1,
    "HEMOGLOBIN_BREST": 1,
    "Beta_thalassemia_intermedia|Beta-thalassemia_HBB/LCRB|Hemoglobinopathy|not_provided|beta_Thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|not_provided|HEMOGLOBIN_BEIRUT": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|HEMOGLOBIN_HOFU": 1,
    "HEMOGLOBIN_MOLFETTA": 1,
    "not_specified|beta_Thalassemia": 2,
    "not_specified|not_provided|HEMOGLOBIN_TENDE": 1,
    "not_provided|Hemoglobinopathy|HEMOGLOBIN_KHARTOUM": 1,
    "Erythrocytosis|_familial|_6|not_provided|HEMOGLOBIN_TY_GARD": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|HEMOGLOBIN_TUNIS": 1,
    "not_provided|beta_Thalassemia|not_specified|HEMOGLOBIN_VILLEJUIF": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|HEMOGLOBIN_ERNZ|beta_Thalassemia": 1,
    "HEMOGLOBIN_BUSHEY": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|HEMOGLOBIN_BEOGRAD|HEMOGLOBIN_D_(CAMPERDOWN)": 1,
    "not_specified|HEMOGLOBIN_ST._FRANCIS": 1,
    "HEMOGLOBIN_D_(NEATH)": 1,
    "Beta-thalassemia_HBB/LCRB|not_provided|Dominant_beta-thalassemia|beta_Thalassemia|Hb_SS_disease": 1,
    "Hemoglobin_D_disease|Beta-thalassemia_HBB/LCRB|HBB-related_disorder|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|not_provided|Hb_D-Los_Angeles|beta_Thalassemia": 1,
    "Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|alpha_Thalassemia|Heinz_body_anemia|Sickle_cell-Hemoglobin_O_Arab_disease|not_provided|HEMOGLOBIN_O_(ARAB)|HEMOGLOBIN_EGYPT|beta_Thalassemia": 1,
    "HEMOGLOBIN_JIANGHUA": 1,
    "not_provided|HEMOGLOBIN_HIJIYAMA": 1,
    "HEMOGLOBIN_TAKAMATSU": 1,
    "HEMOGLOBIN_BOUGARDIREY-MALI": 1,
    "HEMOGLOBIN_IOWA": 1,
    "HEMOGLOBIN_HARROW": 1,
    "HEMOGLOBIN_MINNEAPOLIS-LAOS": 1,
    "HEMOGLOBIN_HAFNIA": 1,
    "beta_Thalassemia|HEMOGLOBIN_P|HEMOGLOBIN_P_(GALVESTON)": 1,
    "HEMOGLOBIN_SAITAMA": 1,
    "HEMOGLOBIN_TSUKUMI": 1,
    "Hemoglobinopathy|not_provided|Dominant_beta-thalassemia": 1,
    "Dominant_beta-thalassemia|HEMOGLOBIN_MADRID": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta_thalassemia_intermedia|HEMOGLOBIN_DURHAM-N.C.|HEMOGLOBIN_BRESCIA": 1,
    "Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_ZENGCHENG": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|not_provided": 1,
    "HEMOGLOBIN_CANTERBURY": 1,
    "HEMOGLOBIN_YAHATA": 1,
    "HEMOGLOBIN_INDIANAPOLIS|Heinz_body_anemia": 1,
    "HEMOGLOBIN_STANMORE": 1,
    "HEMOGLOBIN_PETERBOROUGH": 1,
    "Beta-thalassemia_HBB/LCRB|not_provided|beta_Thalassemia|Beta-plus-thalassemia|HEMOGLOBIN_SHOWA-YAKUSHIJI|Beta-Showa-Yakushiji_thalassemia|Hb_SS_disease": 1,
    "HEMOGLOBIN_MANHATTAN|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_JOHNSTOWN|not_provided": 1,
    "not_provided|Erythrocytosis|_familial|_6|Hemoglobinopathy|HEMOGLOBIN_SAN_DIEGO|beta_Thalassemia": 1,
    "beta_Thalassemia|not_provided|not_specified": 6,
    "not_provided|beta_Thalassemia|Dominant_beta-thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia": 1,
    "HEMOGLOBIN_PRESBYTERIAN": 1,
    "HEMOGLOBIN_YOSHIZUKA": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Inborn_genetic_diseases|not_provided|not_specified|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|Hemoglobin_E": 1,
    "not_provided|Heinz_body_anemia|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Dominant_beta-thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hb_SS_disease|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_BURKE": 1,
    "HEMOGLOBIN_TERRE_HAUTE|Beta-plus-thalassemia": 1,
    "HEMOGLOBIN_SOUTHAMPTON|HEMOGLOBIN_CASPER": 1,
    "METHEMOGLOBINEMIA|_BETA_TYPE": 1,
    "not_specified|HEMOGLOBIN_SOUTH_MILWAUKEE": 1,
    "beta_Thalassemia|not_provided|Beta_zero_thalassemia": 1,
    "not_provided|Beta_zero_thalassemia|beta_Thalassemia|Beta-thalassemia_HBB/LCRB": 2,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|alpha_Thalassemia|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "beta_Thalassemia|Beta-thalassemia_major|Beta_zero_thalassemia|not_provided": 1,
    "not_provided|Malaria|_susceptibility_to|Heinz_body_anemia|METHEMOGLOBINEMIA|_BETA_TYPE|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Dominant_beta-thalassemia|alpha_Thalassemia|Erythrocytosis|_familial|_6": 1,
    "Beta_zero_thalassemia|not_provided|beta_Thalassemia": 1,
    "Beta-plus-thalassemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|alpha_Thalassemia|Heinz_body_anemia|beta_Thalassemia|Beta_thalassemia_intermedia|not_provided|HBB-related_disorder": 1,
    "beta_Thalassemia|not_specified|Beta-thalassemia_HBB/LCRB|not_provided": 1,
    "not_specified|beta_Thalassemia|Beta-thalassemia_HBB/LCRB|not_provided|Hb_SS_disease": 1,
    "beta_Thalassemia|not_provided|Beta-plus-thalassemia": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|not_provided|beta_Thalassemia": 2,
    "Dominant_beta-thalassemia|Malaria|_susceptibility_to|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Heinz_body_anemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|Erythrocytosis|_familial|_6|not_specified|not_provided": 1,
    "not_provided|beta_Thalassemia|not_specified": 3,
    "Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-plus-thalassemia|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|not_provided|beta_Thalassemia|HBB-related_disorder": 1,
    "HBB-related_disorder|beta_Thalassemia|not_provided|not_specified": 1,
    "Beta-plus-thalassemia|not_provided|beta_Thalassemia": 1,
    "Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|HBB-related_disorder|not_provided|Beta-thalassemia_major|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "HBB-related_disorder|not_specified|not_provided": 2,
    "Beta-thalassemia_HBB/LCRB|not_provided": 1,
    "Abnormal_hemoglobin|Persistence_of_hemoglobin_F|Reduced_beta/alpha_synthesis_ratio|Anemia|Hemoglobin_Lepore_trait|alpha_Thalassemia": 1,
    "beta_Thalassemia|.": 1,
    "Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Heinz_body_anemia|not_specified|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_CAMPERDOWN": 1,
    "not_specified|HEMOGLOBIN_SHERWOOD_FOREST": 1,
    "HEMOGLOBIN_HEATHROW|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_SPARTA": 1,
    "HEMOGLOBIN_SAINT_NAZAIRE": 1,
    "HEMOGLOBIN_RICHMOND": 1,
    "not_specified|beta_Thalassemia|not_provided": 1,
    "HEMOGLOBIN_BETH_ISRAEL": 1,
    "HEMOGLOBIN_ST._MANDE": 1,
    "HEMOGLOBIN_POTOMAC|Erythrocytosis|_familial|_6": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_ALBERTA": 1,
    "HEMOGLOBIN_RUSH": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_BRITISH_COLUMBIA": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_BRIGHAM": 1,
    "HEMOGLOBIN_NEW_MEXICO|not_provided": 1,
    "HEMOGLOBIN_COIMBRA": 1,
    "not_specified|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_CHEMILLY|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_HOTEL-DIEU|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_RADCLIFFE|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_YPSILANTI|Erythrocytosis|_familial|_6": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_YAKIMA": 1,
    "HEMOGLOBIN_KEMPSEY|Erythrocytosis|_familial|_6": 1,
    "Hemoglobinopathy|beta_Thalassemia|not_provided": 2,
    "HEMOGLOBIN_NOTTINGHAM": 1,
    "HEMOGLOBIN_DJELFA": 1,
    "HEMOGLOBIN_GALICIA": 1,
    "beta_Thalassemia|Heinz_body_anemia|Hemoglobinopathy|not_provided": 1,
    "HEMOGLOBIN_GUN_HILL|beta_Thalassemia": 1,
    "Hemoglobin_E|Hb_SS_disease|not_specified|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|Inborn_genetic_diseases|not_provided": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_MALMO": 1,
    "Erythrocytosis|_familial|_6|not_provided|HEMOGLOBIN_WOOD": 1,
    "HEMOGLOBIN_NAGOYA": 1,
    "HEMOGLOBIN_MORIGUCHI": 1,
    "HEMOGLOBIN_SANTA_CLARA": 1,
    "Malaria|_susceptibility_to": 7,
    "HEMOGLOBIN_DEBROUSSE": 1,
    "not_provided|Malaria|_susceptibility_to": 2,
    "HEMOGLOBIN_REGINA": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|HEMOGLOBIN_DETROIT": 1,
    "HEMOGLOBIN_J_(CORDOBA)": 1,
    "not_specified|not_provided|beta_Thalassemia|HEMOGLOBIN_HOPKINS_1|HEMOGLOBIN_KENWOOD|HEMOGLOBIN_N_(BALTIMORE)|HEMOGLOBIN_N_(JENKINS)|HEMOGLOBIN_JENKINS": 1,
    "HEMOGLOBIN_CHANDIGARH": 1,
    "Dominant_beta-thalassemia|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_GELDROP_ST._ANNA": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_BARCELONA": 1,
    "not_specified|not_provided|HEMOGLOBIN_BUNBURY": 1,
    "HEMOGLOBIN_OKAZAKI": 1,
    "HEMOGLOBIN_SAINT_ETIENNE": 1,
    "HEMOGLOBIN_MOZHAISK": 1,
    "HEMOGLOBIN_NEWCASTLE": 1,
    "not_provided|METHEMOGLOBINEMIA|_BETA_TYPE|HEMOGLOBIN_M_(MILWAUKEE_2)|HEMOGLOBIN_M_(HYDE_PARK)|HEMOGLOBIN_M_(AKITA)": 1,
    "HEMOGLOBIN_J_(ALTGELD_GARDENS)": 1,
    "not_provided|HEMOGLOBIN_CARIBBEAN": 1,
    "not_specified|HEMOGLOBIN_SABINE": 1,
    "not_specified|Hb_SS_disease|Hemoglobin_E|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|Inborn_genetic_diseases|not_provided": 1,
    "HEMOGLOBIN_PIERRE-BENITE|Hemoglobinopathy": 1,
    "HEMOGLOBIN_ROSEAU-POINTE_A_PITRE": 1,
    "Beta_zero_thalassemia|beta_Thalassemia|not_provided": 2,
    "not_provided|not_specified|beta_Thalassemia|HEMOGLOBIN_AGENOGI": 1,
    "HEMOGLOBIN_VILLAVERDE": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_CRETEIL|beta_Thalassemia": 1,
    "HEMOGLOBIN_VANDERBILT|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_BORAS|HBB-related_disorder": 1,
    "Beta-thalassemia_HBB/LCRB|not_provided|HEMOGLOBIN_SANTA_ANA": 1,
    "HEMOGLOBIN_TOURS": 1,
    "beta_Thalassemia|HEMOGLOBIN_D_(IBADAN)|not_specified": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|beta_Thalassemia|HEMOGLOBIN_VALLETTA": 1,
    "HEMOGLOBIN_OLOMOUC": 1,
    "HEMOGLOBIN_CARDARELLI": 1,
    "Hemoglobin_Lepore_trait": 2,
    "Hemoglobinopathy|not_provided": 2,
    "HEMOGLOBIN_KOFU": 1,
    "not_provided|HEMOGLOBIN_SAALE": 1,
    "Beta-thalassemia_HBB/LCRB|not_provided|beta_Thalassemia": 2,
    "not_specified|HEMOGLOBIN_PYRGOS|not_provided": 1,
    "HEMOGLOBIN_TA-LI|not_provided": 1,
    "not_provided|HEMOGLOBIN_MUSKEGON": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_PROVIDENCE": 1,
    "Erythrocytosis|_familial|_6|not_provided|HEMOGLOBIN_HELSINKI": 1,
    "HEMOGLOBIN_RAHERE|Erythrocytosis|_familial|_6": 1,
    "HEMOGLOBIN_TSURUMAI": 1,
    "beta_Thalassemia|Hb_SS_disease|not_specified|Hemoglobin_E|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1": 1,
    "HEMOGLOBIN_BAYLOR": 1,
    "HEMOGLOBIN_LA_ROCHE-SUR-YON": 1,
    "HEMOGLOBIN_G_(SZUHU)|HEMOGLOBIN_GIFU": 1,
    "beta_Thalassemia|not_specified": 3,
    "not_specified|HEMOGLOBIN_G_(HSI-TSOU)": 1,
    "HEMOGLOBIN_TAMPA|not_provided": 1,
    "not_specified|HEMOGLOBIN_TIGRAYE": 1,
    "HEMOGLOBIN_G_(ACCRA)|not_specified|HEMOGLOBIN_YAIZU": 1,
    "HEMOGLOBIN_QUIN-HAI": 1,
    "not_specified|beta_Thalassemia|Beta-plus-thalassemia|not_provided": 1,
    "Beta-thalassemia_HBB/LCRB|beta_Thalassemia": 1,
    "HEMOGLOBIN_COSTA_RICA": 1,
    "not_specified|beta_Thalassemia|HEMOGLOBIN_FUKUYAMA|not_provided": 1,
    "not_provided|HEMOGLOBIN_J_(IRAN)": 1,
    "HEMOGLOBIN_J_(CHICAGO)": 1,
    "HEMOGLOBIN_ST._ANTOINE": 1,
    "HEMOGLOBIN_CALAIS": 1,
    "HEMOGLOBIN_VICKSBURG": 1,
    "HEMOGLOBIN_PASADENA": 1,
    "HEMOGLOBIN_ATLANTA|HEMOGLOBIN_ATLANTA-COVENTRY": 1,
    "HEMOGLOBIN_MONTREAL": 1,
    "Congenital_anemia|HEMOGLOBIN_BUSHWICK": 1,
    "HEMOGLOBIN_SHEPHERDS_BUSH": 1,
    "HEMOGLOBIN_AALBORG": 1,
    "HEMOGLOBIN_MOBILE": 1,
    "HEMOGLOBIN_TILBURG": 1,
    "beta_Thalassemia|Beta_zero_thalassemia": 5,
    "HEMOGLOBIN_VANCOUVER": 1,
    "not_specified|not_provided|beta_Thalassemia|HEMOGLOBIN_KORLE-BU": 1,
    "Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|Inborn_genetic_diseases|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_CHRISTCHURCH": 1,
    "HEMOGLOBIN_MARINEO|not_specified": 1,
    "HEMOGLOBIN_SEATTLE": 1,
    "not_provided|HEMOGLOBIN_KENITRA": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|alpha_Thalassemia|Hemoglobinopathy|not_provided|not_specified|Hemoglobin_E|HEMOGLOBIN_CITY_OF_HOPE": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|HBB-related_disorder": 1,
    "HEMOGLOBIN_MIZUHO|Atypical_hemolytic-uremic_syndrome": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_BRISBANE|HEMOGLOBIN_GREAT_LAKES": 1,
    "Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|alpha_Thalassemia|Heinz_body_anemia|not_provided|HEMOGLOBIN_ROCKFORD": 1,
    "Dominant_beta-thalassemia|Malaria|_susceptibility_to|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Heinz_body_anemia|alpha_Thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|Erythrocytosis|_familial|_6|not_provided|beta_Thalassemia": 1,
    "not_provided|HEMOGLOBIN_MANUKAU": 1,
    "HEMOGLOBIN_SYDNEY": 1,
    "METHEMOGLOBINEMIA|_BETA_TYPE|HEMOGLOBIN_M_(MILWAUKEE_1)": 1,
    "Hemoglobinopathy|not_provided|HEMOGLOBIN_ALESHA|HEMOGLOBIN_BRISTOL": 1,
    "Dominant_beta-thalassemia|beta_Thalassemia": 1,
    "not_provided|HEMOGLOBIN_CHICO": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Hemoglobinopathy|not_provided|not_specified": 1,
    "HEMOGLOBIN_J_(SICILIA)": 1,
    "HEMOGLOBIN_J_(ANTAKYA)": 1,
    "HEMOGLOBIN_J_(CAIRO)": 1,
    "HEMOGLOBIN_AUBAGNE|not_provided": 1,
    "HEMOGLOBIN_J_(COSENZA)|HEMOGLOBIN_J_(BARI)|HEMOGLOBIN_J_(CALABRIA)": 1,
    ".|not_provided|Hemoglobinopathy": 1,
    "HEMOGLOBIN_BICETRE": 1,
    "HEMOGLOBIN_M_(RADOM)_METHEMOGLOBINEMIA|_BETA_TYPE|HEMOGLOBIN_M_(SASKATOON)|beta_Thalassemia|not_provided|Inborn_genetic_diseases|METHEMOGLOBINEMIA|_BETA_TYPE": 1,
    "HEMOGLOBIN_HANA|METHEMOGLOBINEMIA|_BETA_TYPE": 1,
    "HEMOGLOBIN_J_(EUROPA)": 1,
    "HEMOGLOBIN_DUARTE": 1,
    "not_provided|not_specified|HEMOGLOBIN_HIKARI": 1,
    "HEMOGLOBIN_BOLOGNA": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "not_specified|beta_Thalassemia|HEMOGLOBIN_N_(SEATTLE)|not_provided": 1,
    "HEMOGLOBIN_POCOS_DE_CALDAS": 1,
    "HEMOGLOBIN_COLLINGWOOD": 1,
    "HEMOGLOBIN_CAGLIARI|Beta-plus-thalassemia": 1,
    "HEMOGLOBIN_TOCHIGI": 1,
    "HBB-related_disorder": 2,
    "HEMOGLOBIN_YATSUSHIRO": 1,
    "not_specified|not_provided|beta_Thalassemia|HEMOGLOBIN_J_(LOME)": 1,
    "not_provided|beta_Thalassemia|not_specified|Inborn_genetic_diseases": 1,
    "beta_Thalassemia|not_specified|not_provided": 2,
    "HEMOGLOBIN_I_(HIGH_WYCOMBE)": 1,
    "Hemoglobinopathy|not_provided|beta_Thalassemia": 2,
    "Hemoglobinopathy|not_specified|not_provided": 1,
    "HEMOGLOBIN_G_(FERRARA)|not_provided": 1,
    "HEMOGLOBIN_J_(DALOA)": 1,
    "not_provided|HEMOGLOBIN_HAMADAN": 1,
    "HEMOGLOBIN_MATERA": 1,
    "HEMOGLOBIN_JACKSONVILLE": 1,
    "not_specified|Beta-thalassemia_HBB/LCRB": 1,
    "HEMOGLOBIN_HOKUSETSU": 1,
    "not_provided|HEMOGLOBIN_OCHO_RIOS": 1,
    "beta_Thalassemia|HEMOGLOBIN_SUMMER_HILL|not_specified|not_provided": 1,
    "HEMOGLOBIN_WILLAMETTE": 1,
    "HEMOGLOBIN_EDMONTON": 1,
    "not_specified|not_provided|HEMOGLOBIN_LAS_PALMAS": 1,
    "not_provided|HEMOGLOBIN_COLIMA": 1,
    "HEMOGLOBIN_OKALOOSA": 1,
    "HEMOGLOBIN_BAB-SAADOUN": 1,
    "HEMOGLOBIN_GAVELLO": 1,
    "HEMOGLOBIN_AVICENNA": 1,
    "HEMOGLOBIN_MAPUTO|not_provided": 1,
    "not_specified|not_provided|HEMOGLOBIN_G_(COPENHAGEN)": 1,
    "HEMOGLOBIN_K_(IBADAN)|not_provided|beta_Thalassemia": 1,
    "HEMOGLOBIN_NITEROI": 1,
    "HEMOGLOBIN_GAINESVILLE-GA": 1,
    "beta_Thalassemia|Beta-thalassemia_HBB/LCRB|Hemoglobinopathy|Dominant_beta-thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|HEMOGLOBIN_ARTA": 1,
    "not_specified|not_provided|HEMOGLOBIN_CHEVERLY": 1,
    "Dominant_beta-thalassemia|beta_Thalassemia|Beta_zero_thalassemia|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|not_provided": 1,
    "not_specified|not_provided|HEMOGLOBIN_G_(PORT_ARTHUR)|HEMOGLOBIN_G_(TEXAS)|HEMOGLOBIN_G_(GALVESTON)": 1,
    "Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Heinz_body_anemia|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Hemoglobinopathy|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "beta_Thalassemia|Hemoglobinopathy": 1,
    "Heinz_body_anemia|Hemoglobinopathy|not_provided": 1,
    "Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|HBB-related_disorder|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|alpha_Thalassemia|Inborn_genetic_diseases|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "not_provided|Heinz_body_anemia|HEMOGLOBIN_HAMMERSMITH|HEMOGLOBIN_CHIBA|beta_Thalassemia": 1,
    "HEMOGLOBIN_ILMENAU": 1,
    "HEMOGLOBIN_DENVER|not_provided": 1,
    "HEMOGLOBIN_MEQUON": 1,
    "Heinz_body_anemia|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Dominant_beta-thalassemia|alpha_Thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hb_SS_disease|not_provided|beta_Thalassemia": 1,
    "HEMOGLOBIN_AUSTIN": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|not_specified|not_provided|HEMOGLOBIN_ATHENS-GEORGIA": 1,
    "not_provided|beta_Thalassemia|Beta_zero_thalassemia": 2,
    "HEMOGLOBIN_TIANSHUI": 1,
    "beta_Thalassemia|alpha_Thalassemia|Beta_zero_thalassemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|not_provided|HBB-related_disorder|Inborn_genetic_diseases": 1,
    "HEMOGLOBIN_VAASA": 1,
    "not_provided|HEMOGLOBIN_ALABAMA|beta_Thalassemia": 1,
    "HEMOGLOBIN_LA_CORUNA": 1,
    "not_provided|HEMOGLOBIN_HINWIL": 1,
    "HEMOGLOBIN_HAZEBROUCK": 1,
    "Hemoglobinopathy|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_HIROSE": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Hemoglobinopathy|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 2,
    "not_provided|HEMOGLOBIN_HOWICK": 1,
    "HEMOGLOBIN_ROTHSCHILD": 1,
    "HEMOGLOBIN_SUNNYBROOK": 1,
    "Hypertrophic_cardiomyopathy_26|Erythrocytosis|_familial|_6|HEMOGLOBIN_VILA_REAL": 1,
    "HEMOGLOBIN_NORTH_CHICAGO": 1,
    "HEMOGLOBIN_BRIE_COMTE_ROBERT": 1,
    "HEMOGLOBIN_LINKOPING|HEMOGLOBIN_MEILAHTI": 1,
    "Heinz_body_anemia|Erythrocytosis|_familial|_6|METHEMOGLOBINEMIA|_BETA_TYPE|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Dominant_beta-thalassemia|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|not_specified|not_provided": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|Beta_zero_thalassemia|beta_Thalassemia": 2,
    "HEMOGLOBIN_PHILLY": 1,
    "HEMOGLOBIN_KOREA|Beta-thalassemia_HBB/LCRB": 1,
    "HEMOGLOBIN_SANTANDER": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|Erythrocytosis": 1,
    "not_specified|HEMOGLOBIN_RIO_CLARO": 1,
    "HEMOGLOBIN_CASTILLA": 1,
    "not_provided|HEMOGLOBIN_PERTH|HEMOGLOBIN_ABRAHAM_LINCOLN|HEMOGLOBIN_KOBE": 1,
    "Beta-thalassemia_HBB/LCRB|Inborn_genetic_diseases|not_specified|not_provided|Beta_zero_thalassemia|beta_Thalassemia|Malaria|_susceptibility_to": 1,
    "beta_Thalassemia|Dominant_beta-thalassemia": 1,
    "HEMOGLOBIN_HAKKARI": 1,
    "HEMOGLOBIN_YOKOHAMA": 1,
    "HEMOGLOBIN_MUSCAT": 1,
    "beta_Thalassemia|Beta-thalassemia_HBB/LCRB|not_specified|Heinz_body_anemia|not_provided": 1,
    "Beta-thalassemia_HBB/LCRB|not_provided|Beta-thalassemia_major|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "not_provided|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "Beta-thalassemia_HBB/LCRB|Hemoglobinopathy|beta_Thalassemia|not_provided": 1,
    "not_provided|Beta-plus-thalassemia|Beta_thalassemia_intermedia|beta_Thalassemia": 1,
    "not_provided|Erythrocytosis|_familial|_6|Beta-thalassemia_major|Fetal_hemoglobin_quantitative_trait_locus_1|Beta-plus-thalassemia|beta_Thalassemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|alpha_Thalassemia|Inborn_genetic_diseases": 1,
    "beta_Thalassemia|HBB-related_disorder|Beta-thalassemia_HBB/LCRB|not_provided": 1,
    "not_provided|not_specified|beta_Thalassemia": 1,
    "beta_Thalassemia|Hemoglobinopathy|Beta_zero_thalassemia": 1,
    "Erythrocytosis|_familial|_6|Beta-plus-thalassemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|Beta_thalassemia_intermedia|beta_Thalassemia|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|alpha_Thalassemia|HBB-related_disorder|Inborn_genetic_diseases": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 2,
    "Dominant_beta-thalassemia|not_provided|Hemoglobin_E/beta-_thalassemia|Beta-thalassemia_HBB/LCRB|Beta-thalassemia_major|Beta-plus-thalassemia|Hb_SS_disease|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Malaria|_susceptibility_to|Heinz_body_anemia|beta_Thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|alpha_Thalassemia|HBB-related_disorder|Inborn_genetic_diseases": 1,
    "Malaria|_susceptibility_to|Erythrocytosis|_familial|_6|Hb_SS_disease|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "Beta_zero_thalassemia|beta_Thalassemia|not_specified|not_provided": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "not_provided|beta_Thalassemia|Beta-thalassemia_HBB/LCRB|Beta_zero_thalassemia": 1,
    "Beta-thalassemia_HBB/LCRB|HBB-related_disorder|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|Inborn_genetic_diseases|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|Inborn_genetic_diseases|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|HBB-related_disorder|not_provided|Beta-thalassemia_major|beta_Thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia": 1,
    "not_provided|HEMOGLOBIN_LUFKIN": 1,
    "HEMOGLOBIN_TIZI-OUZOU": 1,
    "HEMOGLOBIN_CHESTERFIELD": 1,
    "HEMOGLOBIN_HYOGO|HEMOGLOBIN_GENOVA|Hemoglobinopathy": 1,
    "HEMOGLOBIN_ST._LOUIS|Heinz_body_anemia": 1,
    "not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|Hb_SS_disease|beta_Thalassemia|Hemoglobin_E|not_specified": 1,
    "HEMOGLOBIN_CHILE": 1,
    "not_provided|HEMOGLOBIN_GRANGE-BLANCHE": 1,
    "HEMOGLOBIN_VOLGA|HEMOGLOBIN_DRENTHE|not_provided": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Hemoglobinopathy|not_provided|beta_Thalassemia|Beta-plus-thalassemia|Beta-Knossos-thalassemia|HEMOGLOBIN_KNOSSOS": 1,
    "HEMOGLOBIN_HENRI_MONDOR": 1,
    "HEMOGLOBIN_TRIPOLI": 1,
    "Beta_zero_thalassemia|beta_Thalassemia": 1,
    "HEMOGLOBIN_HIGASHITOCHIGI|HEMOGLOBIN_HT": 1,
    "not_provided|Hemoglobinopathy|beta_Thalassemia|Beta-thalassemia_HBB/LCRB": 1,
    "Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|HBB-related_disorder|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|beta_Thalassemia|alpha_Thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|Hemoglobin_E/beta-_thalassemia|Hemoglobin_E_disease|Inborn_genetic_diseases|not_specified|not_provided|Hemoglobin_E|Hemoglobin_E/beta_thalassemia_disease|Beta-plus-thalassemia|Malaria|_resistance_to|Anemia": 1,
    "HEMOGLOBIN_J_(AUCKLAND)": 1,
    "HEMOGLOBIN_G_(TAIWAN-AMI)": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|alpha_Thalassemia|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "HEMOGLOBIN_SAVANNAH": 1,
    "HEMOGLOBIN_MOSCVA": 1,
    "HEMOGLOBIN_RIVERDALE-BRONX": 1,
    "HEMOGLOBIN_MIYASHIRO": 1,
    "HEMOGLOBIN_ZOETERWOUDE": 1,
    "HEMOGLOBIN_STRASBOURG|not_provided": 1,
    "Erythrocytosis|_familial|_6|HEMOGLOBIN_PALMERSTON_NORTH": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|HEMOGLOBIN_D_(GRANADA)": 1,
    "not_provided|HEMOGLOBIN_G_(TAIPEI)": 1,
    "not_provided|beta_Thalassemia|HEMOGLOBIN_G_(COUSHATTA)|HEMOGLOBIN_G_(SASKATOON)|HEMOGLOBIN_G_(HSIN-CHU)|HEMOGLOBIN_G_(TAEGU)|not_specified": 1,
    "HEMOGLOBIN_MIYADA|.": 1,
    "not_provided|HEMOGLOBIN_D_(IRAN)|not_specified": 1,
    "not_provided|HEMOGLOBIN_E_(SASKATOON)": 1,
    "HEMOGLOBIN_CONNECTICUT": 1,
    ".|beta_Thalassemia|Beta-thalassemia_HBB/LCRB": 1,
    "not_provided|HEMOGLOBIN_YUSA": 1,
    "HEMOGLOBIN_KARLSKOGA": 1,
    "HEMOGLOBIN_COCODY|not_provided": 1,
    "HEMOGLOBIN_TROLLHAETTAN": 1,
    "Erythrocytosis|_familial|_6|Dominant_beta-thalassemia|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Heinz_body_anemia|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Malaria|_susceptibility_to|Inborn_genetic_diseases|Hemoglobinopathy|not_provided|HEMOGLOBIN_OLYMPIA": 1,
    "HEMOGLOBIN_D_(OULED_RABAH)|not_provided|not_specified": 1,
    "HEMOGLOBIN_LYON": 1,
    "not_provided|Beta-Malay-thalassemia|HEMOGLOBIN_MALAY|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "HEMOGLOBIN_ALAMO|beta_Thalassemia": 1,
    "HEMOGLOBIN_BADEN": 1,
    "HEMOGLOBIN_J_(AMIENS)": 1,
    "Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|beta_Thalassemia|alpha_Thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|not_provided|Beta_zero_thalassemia": 1,
    "HEMOGLOBIN_NAGASAKI": 1,
    "HEMOGLOBIN_NIKOSIA": 1,
    "Beta-thalassemia_HBB/LCRB|HBB-related_disorder|Erythrocytosis|_familial|_6|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Heinz_body_anemia|Inborn_genetic_diseases|Hemoglobinopathy|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 1,
    "not_specified|not_provided|HEMOGLOBIN_J_(BALTIMORE)": 1,
    "HEMOGLOBIN_D_(BUSHMAN)": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta_zero_thalassemia": 2,
    "Beta-thalassemia_HBB/LCRB|beta_Thalassemia|not_provided": 1,
    "beta_Thalassemia|Beta_zero_thalassemia|not_provided|Hemoglobinopathy": 1,
    "HEMOGLOBIN_RANDWICK": 1,
    "HEMOGLOBIN_BELFAST": 1,
    "beta_Thalassemia|HEMOGLOBIN_SOGN|not_specified|not_provided": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|not_provided|HEMOGLOBIN_SAKI|beta_Thalassemia": 1,
    "HEMOGLOBIN_J_(LENS)": 1,
    "Beta_zero_thalassemia|Hemoglobinopathy|not_provided|beta_Thalassemia": 1,
    "HEMOGLOBIN_WINDSOR": 1,
    "HEMOGLOBIN_WASHTENAW|not_provided": 1,
    "Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Beta-thalassemia_HBB/LCRB|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|not_specified|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|HEMOGLOBIN_HAMILTON|Hemoglobin_E": 1,
    "not_provided|beta_Thalassemia|HBB-related_disorder|Inborn_genetic_diseases": 1,
    "HEMOGLOBIN_IRAQ-HALABJA": 1,
    "HEMOGLOBIN_ANKARA": 1,
    "not_specified|HEMOGLOBIN_PORTO_ALEGRE|not_provided": 1,
    "Beta-plus-thalassemia|beta_Thalassemia": 1,
    "HEMOGLOBIN_BREM-SUR-MER": 1,
    "METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|Hb_SS_disease|HBB-related_disorder|Inborn_genetic_diseases|not_provided|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "HEMOGLOBIN_LIMASSOL": 1,
    "Beta_zero_thalassemia|beta_Thalassemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|HBB-related_disorder|not_provided": 1,
    "HEMOGLOBIN_NAKANO": 1,
    "HEMOGLOBIN_LUCKNOW": 1,
    "HEMOGLOBIN_RIO_GRANDE": 1,
    "not_provided|HEMOGLOBIN_N_(TIMONE)": 1,
    "HEMOGLOBIN_J_(LUHE)": 1,
    "HEMOGLOBIN_LEIDEN|not_provided": 1,
    "not_specified|not_provided|HEMOGLOBIN_G_(SAN_JOSE)": 1,
    "beta_Thalassemia|Beta_zero_thalassemia|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|not_provided": 1,
    "Sickle_cell_disease_and_related_diseases|Beta-thalassemia_HBB/LCRB|HBB-related_disorder|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|beta_Thalassemia|alpha_Thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|Inborn_genetic_diseases|not_provided|Sickle_cell-hemoglobin_C_disease|HEMOGLOBIN_S|Malaria|_resistance_to|See_cases": 1,
    "not_specified|HEMOGLOBIN_G_(MAKASSAR)": 1,
    "HEMOGLOBIN_MACHIDA|not_specified": 1,
    "Inherited_hemoglobinopathy|Beta-thalassemia_HBB/LCRB|HBB-related_disorder|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|beta_Thalassemia|alpha_Thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|Inborn_genetic_diseases|not_provided|Sickle_cell-hemoglobin_C_disease|HEMOGLOBIN_C|Malaria|_resistance_to": 1,
    "Dominant_beta-thalassemia|Beta_zero_thalassemia|beta_Thalassemia|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|not_provided|HBB-related_disorder": 1,
    "HEMOGLOBIN_WARWICKSHIRE": 1,
    "beta_Thalassemia|not_specified|not_provided|HEMOGLOBIN_TYNE": 1,
    "HEMOGLOBIN_ANTALYA": 1,
    "Inborn_genetic_diseases|Dominant_beta-thalassemia|Heinz_body_anemia|Malaria|_susceptibility_to|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Erythrocytosis|_familial|_6|alpha_Thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Beta-thalassemia_HBB/LCRB|not_specified|not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|Hemoglobin_E|beta_Thalassemia": 1,
    "not_provided|HEMOGLOBIN_OKAYAMA": 1,
    "not_provided|beta_Thalassemia|Hemoglobinopathy": 1,
    "HEMOGLOBIN_GRAZ": 1,
    "not_provided|HEMOGLOBIN_DEER_LODGE": 1,
    "HEMOGLOBIN_FUKUOKA": 1,
    "HEMOGLOBIN_WATFORD": 1,
    "beta_Thalassemia|not_provided|HEMOGLOBIN_RALEIGH|not_specified": 1,
    "HEMOGLOBIN_DOHA": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|.": 1,
    "beta_Thalassemia|HEMOGLOBIN_SOUTH_FLORIDA|not_provided|not_specified": 1,
    "not_specified|not_provided|Dominant_beta-thalassemia|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|Beta-thalassemia|_lermontov_type|Beta_zero_thalassemia|beta_Thalassemia": 1,
    "Hemoglobinopathy|Heinz_body_anemia|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Dominant_beta-thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hb_SS_disease|not_provided|beta_Thalassemia": 1,
    "Dominant_beta-thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|Hemoglobin_E|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Malaria|_susceptibility_to|Heinz_body_anemia|not_provided|beta_Thalassemia|not_specified|HBB-related_disorder": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|HBB-related_disorder|not_provided|not_specified|beta_Thalassemia": 1,
    "Beta_thalassemia_intermedia|Heinz_body_anemia|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided": 1,
    "Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Malaria|_susceptibility_to|Dominant_beta-thalassemia|Hb_SS_disease|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Heinz_body_anemia|not_provided|Beta-plus-thalassemia|beta_Thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|Beta-plus-thalassemia|beta_Thalassemia": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|Inborn_genetic_diseases|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "not_provided|Beta-plus-thalassemia|beta_Thalassemia": 1,
    "not_specified|not_provided|Beta-plus-thalassemia|beta_Thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta_thalassemia_intermedia|Beta-plus-thalassemia": 1,
    "not_specified|not_provided|Heinz_body_anemia|Malaria|_susceptibility_to|Hereditary_persistence_of_fetal_hemoglobin|Dominant_beta-thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Erythrocytosis|_familial|_6|Hb_SS_disease|beta_Thalassemia|HBB-related_disorder": 1,
    "not_specified|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "beta_Thalassemia|Heinz_body_anemia|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|alpha_Thalassemia|Malaria|_susceptibility_to|not_specified|not_provided": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_specified|not_provided|beta_Thalassemia": 1,
    "Thalassemia": 5,
    "Beta-thalassemia_HBB/LCRB|not_provided|Beta-plus-thalassemia|beta_Thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta_thalassemia_intermedia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|alpha_Thalassemia|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|beta_Thalassemia|Beta-plus-thalassemia|Beta_thalassemia_intermedia": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|alpha_Thalassemia|Fetal_hemoglobin_quantitative_trait_locus_1|beta_Thalassemia|not_provided|Beta_thalassemia_intermedia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Inborn_genetic_diseases|Hemoglobinopathy|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "beta_Thalassemia|Beta-thalassemia_HBB/LCRB|not_provided|Beta-plus-thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|alpha_Thalassemia|Heinz_body_anemia|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Fetal_hemoglobin_quantitative_trait_locus_1|Hb_SS_disease|Malaria|_susceptibility_to|Hemoglobinopathy|not_specified": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|HBB-related_disorder|not_provided|beta_Thalassemia|Beta-plus-thalassemia|Beta_thalassemia_intermedia": 1,
    "beta_Thalassemia|not_specified|Heinz_body_anemia|Hb_SS_disease|METHEMOGLOBINEMIA|_BETA_TYPE|Beta-thalassemia_HBB/LCRB|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|not_provided|Beta_thalassemia_intermedia|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "Malaria|_susceptibility_to|Dominant_beta-thalassemia|Erythrocytosis|_familial|_6|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|METHEMOGLOBINEMIA|_BETA_TYPE|Hb_SS_disease|Heinz_body_anemia|HBB-related_disorder|not_provided|beta_Thalassemia|Beta-plus-thalassemia": 1,
    "Hb_SS_disease|Erythrocytosis|_familial|_6|Heinz_body_anemia|Beta-thalassemia_HBB/LCRB|METHEMOGLOBINEMIA|_BETA_TYPE|Dominant_beta-thalassemia|Hereditary_persistence_of_fetal_hemoglobin|Malaria|_susceptibility_to|Beta-plus-thalassemia": 1,
    "alpha_Thalassemia|METHEMOGLOBINEMIA|_BETA_TYPE|Erythrocytosis|_familial|_6|Dominant_beta-thalassemia|Heinz_body_anemia|Malaria|_susceptibility_to|Beta-thalassemia_HBB/LCRB|Hereditary_persistence_of_fetal_hemoglobin|Hb_SS_disease|not_provided": 1,
    "delta_Thalassemia": 5,
    "HBD-related_disorder": 2,
    "Fetal_hemoglobin_quantitative_trait_locus_1": 13,
    "HEMOGLOBIN_A(2)_MONREALE": 1,
    "HEMOGLOBIN_A(2)_FITZROY": 1,
    "HEMOGLOBIN_A(2)_PELENDRI": 1,
    "not_provided|HEMOGLOBIN_A(2)_BABINGA": 1,
    "HEMOGLOBIN_A(2)_NINIVE": 1,
    "HEMOGLOBIN_A(2)_ZAGREB": 1,
    "HEMOGLOBIN_A(2)_MANZANARES": 1,
    "HEMOGLOBIN_A(2)_COBURG": 1,
    "HEMOGLOBIN_A(2)_CORFU|HEMOGLOBIN_A(2)_TROODOS|Thalassemia": 1,
    "not_provided|delta_Thalassemia": 1,
    "HBD-related_disorder|not_provided": 1,
    "HEMOGLOBIN_A(2)_CAPRI": 1,
    "HEMOGLOBIN_A(2)_CANADA": 1,
    "HEMOGLOBIN_A(2)_WRENS": 1,
    "not_provided|HBD-related_disorder": 1,
    "HEMOGLOBIN_A(2)_SANT'_ANTIOCO": 1,
    "HEMOGLOBIN_A(2)_HONAI": 1,
    "HEMOGLOBIN_A(2)_LUCANIA": 1,
    "HEMOGLOBIN_A(2)_GROVETOWN|delta_Thalassemia": 1,
    "Fetal_hemoglobin_quantitative_trait_locus_1|not_provided": 1,
    "HEMOGLOBIN_A(2)_INDONESIA": 1,
    "Delta-0-thalassemia": 2,
    "HEMOGLOBIN_A(2)_CAMPANIA": 1,
    "HEMOGLOBIN_A(2)_ADRIA": 1,
    "HEMOGLOBIN_A(2)_PARKVILLE": 1,
    "HEMOGLOBIN_A(2)_AGRINIO": 1,
    "HEMOGLOBIN_A(2)_MELBOURNE": 1,
    "HEMOGLOBIN_A(2)_METAPONTO": 1,
    "not_provided|Fetal_hemoglobin_quantitative_trait_locus_1|Thalassemia|delta_Thalassemia|HEMOGLOBIN_A(2)_YIALOUSA|Glucocorticoid-remediable_aldosteronism": 1,
    "HEMOGLOBIN_A(2)_PUGLIA": 1,
    "HEMOGLOBIN_A(2)_YOKOSHIMA": 1,
    "HEMOGLOBIN_A(2)_VICTORIA": 1,
    "HEMOGLOBIN_A(2)_FLATBUSH|HEMOGLOBIN_FLATBUSH_(GEORGIA)": 1,
    "HEMOGLOBIN_A(2)_ROOSEVELT": 1,
    "HEMOGLOBIN_A(2)-PRIME|HEMOGLOBIN_B(2)": 1,
    "HEMOGLOBIN_A(2)_NYU|HEMOGLOBIN_NYU": 1,
    "not_provided|Thalassemia": 1,
    "HEMOGLOBIN_A(2)_SPHAKIA": 1,
    "HEMOGLOBIN_A(2)_NIIGATA": 1,
    "Delta-plus-thalassemia": 1,
    "Delta-beta-thalassemia|not_provided|HBD-related_disorder": 1,
    "HBG1-related_disorder": 2,
    "Hereditary_persistence_of_fetal_hemoglobin|not_provided": 4,
    "not_provided|Hereditary_persistence_of_fetal_hemoglobin": 1,
    "HEMOGLOBIN_F_(JIANGSU)": 1,
    "HEMOGLOBIN_F_(BASKENT)": 1,
    "not_specified|Hereditary_persistence_of_fetal_hemoglobin": 1,
    "Fetal_hemoglobin_quantitative_trait_locus_1|HEMOGLOBIN_F_(SIENA)|HEMOGLOBIN_F_(HULL)": 1,
    "HEMOGLOBIN_F_(DICKINSON)": 1,
    "HEMOGLOBIN_F_(VICTORIA_JUBILEE)": 1,
    "HEMOGLOBIN_F_(YAMAGUCHI)": 1,
    "HEMOGLOBIN_F_(DAMMAM)": 1,
    "Hereditary_persistence_of_fetal_hemoglobin|not_provided|not_specified|HEMOGLOBIN_F_(SARDINIA)|HBG1_POLYMORPHISM": 1,
    "HEMOGLOBIN_F_(XIN-SU)": 1,
    "HEMOGLOBIN_F_(FOREST_PARK)": 1,
    "HEMOGLOBIN_F_(IWATA)": 1,
    "Hereditary_persistence_of_fetal_hemoglobin": 13,
    "HEMOGLOBIN_F_(JAMAICA)": 1,
    "HEMOGLOBIN_F_(BEECH_ISLAND)": 1,
    "HEMOGLOBIN_F_(FUKUYAMA)": 1,
    "Hereditary_persistence_of_fetal_hemoglobin|HEMOGLOBIN_F_(WOODSTOCK)": 1,
    "Hereditary_persistence_of_fetal_hemoglobin|HEMOGLOBIN_F_(BONAIRE)": 1,
    "HEMOGLOBIN_F_(COBB)": 1,
    "HEMOGLOBIN_F_(PENDERGRASS)": 1,
    "HEMOGLOBIN_F_(XINJIANG)": 1,
    "HEMOGLOBIN_F_(KUALA_LUMPUR)": 1,
    "HEMOGLOBIN_F_(CALLUNA)": 1,
    "HEMOGLOBIN_F_(KOTOBUKI)|HEMOGLOBIN_F_(IZUMI)": 1,
    "HEMOGLOBIN_F_(PORDENONE)": 1,
    "Hereditary_persistence_of_fetal_hemoglobin|HEMOGLOBIN_F_(TEXAS_I)": 1,
    "HEMOGLOBIN_F_(MACEDONIA-I)": 1,
    "Hereditary_persistence_of_fetal_hemoglobin-beta-thalassemia_syndrome|Hereditary_persistence_of_fetal_hemoglobin|not_specified": 1,
    "Sardinian_HPFH|Greek_HPFH|Hereditary_persistence_of_fetal_hemoglobin": 1,
    "Hereditary_persistence_of_fetal_hemoglobin|British_HPFH": 1,
    "HEMOGLOBIN_F_(ONODA)": 1,
    "HEMOGLOBIN_F_(POOLE)": 1,
    "HEMOGLOBIN_F_(PORT_ROYAL)": 1,
    "HEMOGLOBIN_F_(CARLTON)": 1,
    "HEMOGLOBIN_F_(CALTECH)": 1,
    "HEMOGLOBIN_F_(CALABRIA)": 1,
    "HEMOGLOBIN_F_(MALTA)": 1,
    "HEMOGLOBIN_F_(MACEDONIA_II)": 1,
    "HEMOGLOBIN_F_(LA_GRANGE)": 1,
    "HEMOGLOBIN_F_(COLUMBUS-GA)": 1,
    "not_provided|Cyanosis|_transient_neonatal": 3,
    "HEMOGLOBIN_F_(MARIETTA)": 1,
    "HEMOGLOBIN_F_(KENNESTONE)": 1,
    "HEMOGLOBIN_F_(LESVOS)|HEMOGLOBIN_F_(WAYNESBORO)": 1,
    "HEMOGLOBIN_F_(MINOO)": 1,
    "Cyanosis|_transient_neonatal": 4,
    "HEMOGLOBIN_F_(SHANGHAI)": 1,
    "not_provided|HEMOGLOBIN_F_(BROOKLYN)": 1,
    "HEMOGLOBIN_F_(CLARKE)": 1,
    "not_provided|HEMOGLOBIN_F_(EMIRATES)": 1,
    "HEMOGLOBIN_F_(SACROMONTE)": 1,
    "HEMOGLOBIN_F_(KINGSTON)": 1,
    "HEMOGLOBIN_F_(LODZ)": 1,
    "not_provided|HEMOGLOBIN_F_(AUSTELL)": 1,
    "HEMOGLOBIN_F_(VELETA)": 1,
    "HEMOGLOBIN_F_(TOKYO)": 1,
    "HEMOGLOBIN_F_(OAKLAND)": 1,
    "HEMOGLOBIN_F_(COSENZA)": 1,
    "HEMOGLOBIN_F_(GRANADA)": 1,
    "HEMOGLOBIN_F_(URUMQI)": 1,
    "HEMOGLOBIN_F_(FUCHU)": 1,
    "HEMOGLOBIN_F_(OULED_RABAH)": 1,
    "HEMOGLOBIN_F_(CLAMART)": 1,
    "not_provided|HEMOGLOBIN_F_(MELBOURNE)": 1,
    "HEMOGLOBIN_F_(CATALONIA)": 1,
    "HEMOGLOBIN_F_(HEATHER)": 1,
    "HEMOGLOBIN_F_(ALBAICIN)": 1,
    "HEMOGLOBIN_F_(AUCKLAND)": 1,
    "HEMOGLOBIN_F_(MEINOHAMA)": 1,
    "HEMOGLOBIN_F_(MALAYSIA)": 1,
    "not_provided|Hereditary_persistence_of_fetal_hemoglobin|not_specified": 1,
    "HBE1-related_disorder": 4,
    "TRIM22-related_disorder": 3,
    "not_provided|TRIM22-related_disorder": 1,
    "not_specified|TRIM22-related_disorder": 2,
    "TRIM22-related_disorder|not_specified": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 279,
    "Niemann-Pick_disease|_type_A": 131,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 295,
    "not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|SMPD1-related_disorder": 1,
    "Sphingomyelin/cholesterol_lipidosis": 15,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 6,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided": 4,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|SMPD1-related_disorder|Inborn_genetic_diseases": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 11,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis": 9,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|SMPD1-related_disorder": 9,
    "Niemann-Pick_disease|_type_A|not_provided|not_specified|SMPD1-related_disorder|Niemann-Pick_disease|_type_B": 1,
    "not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Gaucher_disease": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Intellectual_disability": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 9,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 1,
    "SMPD1-related_disorder|not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 1,
    "not_provided|SMPD1-related_disorder|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_specified": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|not_specified": 2,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_specified": 1,
    "Inborn_genetic_diseases|SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 4,
    "SMPD1-related_disorder|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 3,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|not_provided": 2,
    "Niemann-Pick_disease|_type_A|not_specified|not_provided|Niemann-Pick_disease|_type_B": 1,
    "SMPD1-related_disorder": 9,
    "not_specified|Niemann-Pick_disease|_type_A|not_provided|Niemann-Pick_disease|_type_B": 2,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|SMPD1-related_disorder|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_specified|not_provided": 5,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_specified|not_provided": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided": 16,
    "not_provided|Niemann-Pick_disease|_type_A": 7,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis": 8,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases": 4,
    "Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_B": 3,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Inborn_genetic_diseases": 4,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided": 1,
    "Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|Niemann-Pick_disease|_type_B|not_provided": 1,
    "Sphingomyelin/cholesterol_lipidosis|not_provided|Inborn_genetic_diseases|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 1,
    "Niemann-Pick_disease|_type_B": 6,
    "Inborn_genetic_diseases|Sphingomyelin/cholesterol_lipidosis|not_provided": 1,
    "Niemann-Pick_disease|_type_A|Inborn_genetic_diseases": 2,
    "Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis|SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Inborn_genetic_diseases|not_provided": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_specified": 4,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 7,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_A": 2,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|not_provided": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_specified|not_provided|Sphingomyelin/cholesterol_lipidosis|SMPD1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Niemann-Pick_disease|_type_B": 2,
    "Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis|not_provided": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis|Inborn_genetic_diseases|not_provided|SMPD1-related_disorder": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|SMPD1-related_disorder|Inborn_genetic_diseases": 2,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|not_specified|Sphingomyelin/cholesterol_lipidosis": 1,
    "Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis": 2,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 3,
    "Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|Niemann-Pick_disease|_type_B": 1,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 3,
    "not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis|SMPD1-related_disorder": 1,
    "not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Inborn_genetic_diseases": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Acid_sphingomyelinase_deficiency|not_specified": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis": 9,
    "Niemann-Pick_disease|_type_A|not_provided": 2,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Inborn_genetic_diseases": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis|not_provided": 2,
    "not_specified|not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases": 1,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 3,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 2,
    "Acid_sphingomyelinase_deficiency": 2,
    "Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|SMPD1-related_disorder": 3,
    "not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Sphingomyelin/cholesterol_lipidosis|not_provided|Inborn_genetic_diseases": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis|SMPD1-related_disorder|Inborn_genetic_diseases|Niemann-Pick_disease|_type_B": 1,
    "Niemann-Pick_disease|_type_A|not_provided|not_specified|Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A": 1,
    "not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 8,
    "not_provided|not_specified|Sphingomyelin/cholesterol_lipidosis|SMPD1-related_disorder": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Sphingomyelin/cholesterol_lipidosis|not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|SMPD1-related_disorder": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Acid_sphingomyelinase_deficiency": 1,
    "not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis": 1,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis": 2,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Intellectual_disability": 1,
    "SMPD1-related_disorder|Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 1,
    "Sphingomyelin/cholesterol_lipidosis|not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 1,
    "Inborn_genetic_diseases|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 4,
    "SMPD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 1,
    "Inborn_genetic_diseases|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-pick_disease|_intermediate|_protracted_neurovisceral": 1,
    "not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 2,
    "not_specified|not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 6,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 5,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_specified": 2,
    "Acid_sphingomyelinase_deficiency|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_provided|Sphingomyelin/cholesterol_lipidosis|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "not_provided|SMPD1-related_disorder": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|SMPD1-related_disorder": 3,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Inborn_genetic_diseases": 1,
    "Sphingomyelin/cholesterol_lipidosis|Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_A|SMPD1-related_disorder": 1,
    "Niemann-Pick_disease|_type_A|not_specified|Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|SMPD1-related_disorder": 1,
    "SMPD1-related_disorder|not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided": 1,
    "SMPD1-related_disorder|not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-pick_disease|_intermediate|_protracted_neurovisceral": 1,
    "Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_B|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|not_provided": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_specified|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Niemann-Pick_disease|_type_B": 1,
    "Niemann-Pick_disease|_type_A|not_provided|Niemann-Pick_disease|_type_B": 3,
    "Niemann-Pick_disease|_type_A|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|not_provided": 1,
    "Niemann-Pick_disease|_type_A|Acid_sphingomyelinase_deficiency": 1,
    "not_specified|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|not_provided|Niemann-Pick_disease|_type_B": 1,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_specified|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "SMPD1-related_disorder|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_specified|not_provided": 1,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_specified": 1,
    "not_specified|not_provided|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A": 1,
    "SMPD1-related_disorder|Inborn_genetic_diseases|not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_specified|Niemann-Pick_disease|_type_A": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis|Abnormality_of_metabolism/homeostasis": 1,
    "SMPD1-related_disorder|Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|SMPD1-related_disorder|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|SMPD1-related_disorder|Inborn_genetic_diseases": 1,
    "SMPD1-related_disorder|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis": 2,
    "Niemann-Pick_disease|_type_A|not_specified|Niemann-Pick_disease|_type_B": 1,
    "SMPD1-related_disorder|Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "Niemann-Pick_disease|_type_A|not_provided|not_specified|Niemann-Pick_disease|_type_B": 1,
    "not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_C1|See_cases": 1,
    "not_specified|not_provided|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Niemann-Pick_disease|_type_B": 1,
    "not_specified|not_provided|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "Acid_sphingomyelinase_deficiency|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 1,
    "not_specified|SMPD1-related_disorder|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B|not_provided": 1,
    "not_provided|SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|Inborn_genetic_diseases|Sphingomyelin/cholesterol_lipidosis": 1,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_A": 1,
    "Niemann-Pick_disease|_type_A|not_specified|Niemann-Pick_disease|_type_B|not_provided": 1,
    "not_provided|SMPD1-related_disorder|not_specified|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "not_provided|Inborn_genetic_diseases|Niemann-Pick_disease|_type_A|Niemann-Pick_disease|_type_B": 1,
    "SMPD1-related_disorder|not_specified|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|Sphingomyelin/cholesterol_lipidosis": 1,
    "SMPD1-related_disorder|Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|not_provided|not_specified": 1,
    "Niemann-Pick_disease|_type_B|Niemann-Pick_disease|_type_A|SMPD1-related_disorder|Sphingomyelin/cholesterol_lipidosis": 1,
    "APBB1-related_disorder": 4,
    "not_specified|APBB1-related_disorder": 1,
    "not_specified|TRIM3-related_disorder": 1,
    "DNHD1-related_disorder|not_provided": 27,
    "not_specified|not_provided|DNHD1-related_disorder": 3,
    "not_provided|DNHD1-related_disorder": 35,
    "DNHD1-related_disorder": 57,
    "not_provided|Spermatogenic_failure_65": 3,
    "Spermatogenic_failure_65": 24,
    "Male_infertility_with_spermatogenesis_disorder|not_provided": 1,
    "not_specified|DNHD1-related_disorder": 3,
    "Essential_tremor|DNHD1-related_disorder|Spermatogenic_failure_65|not_provided": 1,
    "DNHD1-related_disorder|not_specified|not_provided": 1,
    "Spermatogenic_failure_65|not_provided|DNHD1-related_disorder": 1,
    "DNHD1-related_disorder|Spermatogenic_failure_65|not_provided": 1,
    "not_specified|DNHD1-related_disorder|not_provided": 1,
    "DNHD1-related_Neurodevelopmental_Disorder": 1,
    "DNHD1-related_disorder|not_provided|not_specified": 1,
    "not_provided|DNHD1-related_disorder|not_specified": 1,
    "DNHD1-related_Intellectual_Disability": 1,
    "Spermatogenic_failure_65|not_specified": 1,
    "DNHD1-related_disorder|not_provided|Male_infertility_with_spermatogenesis_disorder": 1,
    "DNHD1-related_Intellectual_Disability|not_specified": 1,
    "not_provided|not_specified|DNHD1-related_disorder": 2,
    "not_specified|DNHD1-related_Neurodevelopmental_Disorder": 1,
    "DNHD1-related_disorder|Spermatogenic_failure_65": 1,
    "ILK-related_disorder|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "Primary_familial_hypertrophic_cardiomyopathy|not_specified": 24,
    "ILK-related_disorder|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ILK-related_disorder|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "not_provided|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "not_specified|not_provided|Long_QT_syndrome|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 2,
    "ILK-related_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|not_provided": 3,
    "ILK-related_disorder|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ILK-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|ILK-related_disorder|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ILK-related_disorder|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "ILK-related_disorder|not_specified|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|ILK-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis_2": 123,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided": 59,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2": 65,
    "not_provided|Neuronal_Ceroid-Lipofuscinosis|_Recessive": 4,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_provided": 6,
    "Juvenile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis|not_provided|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2": 1,
    "not_specified|not_provided|TPP1-related_disorder|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7": 7,
    "not_provided|TPP1-related_disorder": 3,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases": 7,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7": 7,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Autosomal_recessive_spinocerebellar_ataxia_7": 4,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2|not_provided": 5,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Neuronal_ceroid_lipofuscinosis|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_2": 8,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_2": 3,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided": 7,
    "Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|not_provided": 5,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_7|not_specified|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_7|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "TPP1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2": 8,
    "Inborn_genetic_diseases|Seizure|not_provided|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|not_specified": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Abnormality_of_the_nervous_system|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_2": 2,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2": 2,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|not_specified|Neuronal_ceroid_lipofuscinosis_2": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases|not_specified": 1,
    "TPP1-related_disorder|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Neuronal_ceroid_lipofuscinosis|TPP1-related_disorder|not_provided": 1,
    "not_specified|TPP1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_2|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2": 1,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2|not_specified": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_2|not_provided|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Neuronal_ceroid_lipofuscinosis|not_provided": 3,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases|not_provided": 3,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Inborn_genetic_diseases": 3,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|Neuronal_ceroid_lipofuscinosis_2|not_specified|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_specified": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_2|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Neuronal_ceroid_lipofuscinosis": 2,
    "not_provided|TPP1-related_disorder|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Abnormality_of_the_nervous_system": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|Neuronal_ceroid_lipofuscinosis_2": 1,
    "TPP1-related_disorder|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis|not_provided|Abnormality_of_the_nervous_system": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "TPP1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis_2|not_specified|not_provided": 2,
    "TPP1-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TPP1-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|not_specified": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_2|Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_provided|Neuronal_ceroid_lipofuscinosis|Angelman_syndrome": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_2|not_provided|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_2|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_2": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_7|Neuronal_ceroid_lipofuscinosis_2|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2|TPP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_2|Autosomal_recessive_spinocerebellar_ataxia_7|not_specified|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_7": 1,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_2|Inborn_genetic_diseases": 1,
    "not_provided|TPP1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Neuronal_Ceroid-Lipofuscinosis|_Recessive": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_specified": 1,
    "not_provided|DCHS1-related_disorder": 26,
    "Mitral_valve_prolapse|_myxomatous_2": 6,
    "DCHS1-related_disorder|not_provided": 30,
    "Van_Maldergem_syndrome_1": 25,
    "DCHS1-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "DCHS1-related_disorder": 17,
    "not_provided|Van_Maldergem_syndrome_1|Inborn_genetic_diseases": 4,
    "DCHS1-related_congenital_anomalies_of_the_kidney_and_urinary_tract|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Mitral_valve_prolapse|_myxomatous_2": 4,
    "Inborn_genetic_diseases|DCHS1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|DCHS1-related_disorder": 5,
    "Myoepithelial_tumor|not_provided": 1,
    "not_provided|Van_Maldergem_syndrome_1": 6,
    "Inborn_genetic_diseases|Congenital_heart_disease|not_provided": 2,
    "Mitral_valve_prolapse|_myxomatous_2|Van_Maldergem_syndrome_1": 1,
    "Van_Maldergem_syndrome_1|not_provided": 6,
    "Van_Maldergem_syndrome_1|Mitral_valve_prolapse|_myxomatous_2|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Van_Maldergem_syndrome_1|not_provided": 2,
    "not_provided|Van_Maldergem_syndrome_1|Mitral_valve_prolapse|_myxomatous_2|Inborn_genetic_diseases": 2,
    "DCHS1-related_disorder|not_provided|Inborn_genetic_diseases": 4,
    "Van_Maldergem_syndrome_1|Mitral_valve_prolapse|_myxomatous_2|not_provided": 2,
    "not_provided|DCHS1-related_disorder|Inborn_genetic_diseases": 5,
    "Congenital_heart_disease|Mitral_valve_prolapse|_myxomatous_2|Van_Maldergem_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Mitral_valve_prolapse|_myxomatous_2|not_provided": 3,
    "not_provided|Mitral_valve_prolapse|_myxomatous_2|Van_Maldergem_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|DCHS1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|DCHS1-related_disorder": 3,
    "not_provided|not_specified|DCHS1-related_disorder": 1,
    "Mitral_valve_prolapse|_myxomatous_2|Inborn_genetic_diseases|not_provided": 2,
    "Congenital_heart_disease|Inborn_genetic_diseases|not_provided": 1,
    "Van_Maldergem_syndrome_1|not_specified|not_provided": 2,
    "Van_Maldergem_syndrome_1|not_provided|Inborn_genetic_diseases": 2,
    "Van_Maldergem_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Van_Maldergem_syndrome_1|Mitral_valve_prolapse|_myxomatous_2": 1,
    "not_provided|Van_Maldergem_syndrome_1|not_specified": 2,
    "Mitral_valve_prolapse|_myxomatous_2|not_provided|Inborn_genetic_diseases": 1,
    "DCHS1-related_disorder|not_specified|not_provided": 2,
    "DCHS1-related_disorder|not_provided|not_specified": 1,
    "Van_Maldergem_syndrome_1|DCHS1-related_disorder|not_provided": 1,
    "not_provided|Van_Maldergem_syndrome_1|Mitral_valve_prolapse|_myxomatous_2": 1,
    "not_specified|DCHS1-related_disorder|not_provided": 1,
    "Van_Maldergem_syndrome_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Van_Maldergem_syndrome_1|not_provided": 2,
    "Van_Maldergem_syndrome_1|not_provided|DCHS1-related_disorder": 1,
    "not_provided|Lymphedema": 2,
    "Inborn_genetic_diseases|DCHS1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Van_Maldergem_syndrome_1|Mitral_valve_prolapse|_myxomatous_2": 1,
    "not_provided|Mitral_valve_prolapse|_myxomatous_2|Van_Maldergem_syndrome_1": 1,
    "Van_Maldergem_syndrome_1|not_specified": 1,
    "Van_Maldergem_syndrome_1|not_provided|not_specified": 1,
    "not_provided|Congenital_heart_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mitral_valve_prolapse|_myxomatous_2|not_provided": 1,
    "DCHS1-related_disorder|not_provided|Van_Maldergem_syndrome_1": 1,
    "Inborn_genetic_diseases|Lymphedema": 1,
    "Inborn_genetic_diseases|not_provided|Van_Maldergem_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Van_Maldergem_syndrome_1": 1,
    "not_specified|not_provided|Van_Maldergem_syndrome_1|Congenital_heart_disease": 1,
    "NLRP14-related_disorder": 18,
    "not_provided|NLRP14-related_disorder": 5,
    "not_specified|NLRP14-related_disorder|Spermatogenic_Failure|not_provided": 1,
    "NLRP14-related_disorder|not_provided": 4,
    "PPFIBP2-related_disorder|not_provided": 1,
    "PPFIBP2-related_disorder": 2,
    "EIF3F-related_disorder": 11,
    "EIF3F-related_disorder|not_provided": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_67": 6,
    "not_provided|EIF3F-related_disorder": 3,
    "EIF3F-related_disorder|Intellectual_developmental_disorder|_autosomal_recessive_67|not_provided": 1,
    "EIF3F-related_disorder|Intellectual_developmental_disorder|_autosomal_recessive_67": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_67|EIF3F-related_disorder|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_67|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_67": 2,
    "TUB-related_disorder": 65,
    "TUB-related_disorder|not_provided": 59,
    "not_provided|TUB-related_disorder": 48,
    "TUB-related_disorder|not_specified|not_provided": 5,
    "Retinal_dystrophy_and_obesity": 5,
    "not_provided|TUB-related_disorder|not_specified": 2,
    "TUB-related_disorder|not_provided|Retinal_dystrophy_and_obesity": 3,
    "not_specified|not_provided|TUB-related_disorder|Retinal_dystrophy_and_obesity": 2,
    "not_specified|not_provided|TUB-related_disorder": 4,
    "not_provided|not_specified|TUB-related_disorder": 1,
    "not_specified|TUB-related_disorder|Retinal_dystrophy_and_obesity|not_provided": 1,
    "not_specified|TUB-related_disorder|not_provided": 1,
    "not_provided|Retinal_dystrophy_and_obesity": 6,
    "TUB-related_disorder|not_provided|not_specified": 3,
    "TUB-related_disorder|Retinal_dystrophy_and_obesity|not_provided": 4,
    "TUB-related_disorder|not_specified": 1,
    "Retinal_dystrophy_and_obesity|not_provided": 1,
    "not_specified|TUB-related_disorder": 3,
    "Retinal_dystrophy|not_provided|TUB-related_disorder": 1,
    "not_provided|Retinal_dystrophy_and_obesity|not_specified": 1,
    "not_provided|TUB-related_disorder|Retinal_dystrophy_and_obesity": 2,
    "not_provided|Retinal_dystrophy_and_obesity|not_specified|TUB-related_disorder|Retinal_dystrophy": 1,
    "not_provided|TUB-related_disorder|Retinal_dystrophy": 1,
    "RIC3-related_disorder": 1,
    "LMO1-related_disorder|not_specified": 1,
    "Neuroblastoma|_susceptibility_to|_7|LMO1_POLYMORPHISM": 1,
    "Spermatogenic_failure_93": 1,
    "DENND5A-related_disorder": 2,
    "DENND5A-related_disorder|not_provided": 8,
    "Developmental_and_epileptic_encephalopathy|_49": 15,
    "not_provided|DENND5A-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_49|not_provided": 7,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_49|not_provided": 2,
    "DENND5A-related_disorder|Developmental_and_epileptic_encephalopathy|_49|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_49|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_49|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_49": 1,
    "not_provided|ZNF143-related_disorder": 7,
    "ZNF143-related_disorder|not_provided": 4,
    "Charcot-Marie-Tooth_disease_type_4B2": 71,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B2": 8,
    "Charcot-Marie-Tooth_disease_type_4B2|not_provided": 5,
    "Charcot-Marie-Tooth_disease_type_4|SBF2-related_disorder": 4,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_provided": 1,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "SBF2-related_disorder": 7,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4": 17,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2": 17,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Tip-toe_gait|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|SBF2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2": 2,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_specified": 1,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Congenital_thrombocytopenia|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B2|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Peripheral_neuropathy": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2": 3,
    "Charcot-Marie-Tooth_disease_type_4B2|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 5,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease_type_4": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4B2|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|not_specified": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "SBF2-related_disorder|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 4,
    "not_provided|not_specified|SBF2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases|not_provided": 1,
    "SBF2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4": 6,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2": 2,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease": 1,
    "Tip-toe_gait|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2": 3,
    "Charcot-Marie-Tooth_disease_type_4B2|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B2|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 3,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|SBF2-related_disorder|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Tip-toe_gait": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4|not_specified": 2,
    "not_specified|SBF2-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_provided|Inborn_genetic_diseases": 1,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B2|Tip-toe_gait": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases|Tip-toe_gait|not_specified|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4B2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4B2|not_provided|SBF2-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4B2|SBF2-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease_type_4|SBF2-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B2|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "SBF2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2|not_specified|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4B2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B2": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4B2|SBF2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Erythrocyte_AMP_deaminase_deficiency": 75,
    "not_provided|Erythrocyte_AMP_deaminase_deficiency": 19,
    "AMPD3-related_disorder": 9,
    "Erythrocyte_AMP_deaminase_deficiency|AMPD3-related_disorder": 2,
    "not_provided|not_specified|Erythrocyte_AMP_deaminase_deficiency": 2,
    "not_specified|AMPD3-related_disorder|Erythrocyte_AMP_deaminase_deficiency|not_provided": 1,
    "not_provided|AMPD3-related_disorder|Erythrocyte_AMP_deaminase_deficiency": 1,
    "Erythrocyte_AMP_deaminase_deficiency|not_provided": 4,
    "AMPD3-related_disorder|not_specified|not_provided|Erythrocyte_AMP_deaminase_deficiency": 1,
    "not_specified|not_provided|Erythrocyte_AMP_deaminase_deficiency": 1,
    "not_provided|Erythrocyte_AMP_deaminase_deficiency|AMPD3-related_disorder": 1,
    "Erythrocyte_AMP_deaminase_deficiency|not_specified": 4,
    "Adenosine_monophosphate_deaminase_deficiency": 1,
    "not_specified|Erythrocyte_AMP_deaminase_deficiency": 1,
    "not_provided|not_specified|AMPD3-related_disorder|Erythrocyte_AMP_deaminase_deficiency": 1,
    "CTR9-related_disorder": 4,
    "CTR9-related_neurodevelopmental_disorder": 9,
    "not_provided|Predisposition_to_Wilms_tumor": 3,
    "CTR9-related_disorder|not_provided": 16,
    "CTR9-related_neurodevelopmental_disorder|not_provided": 1,
    "CTR9-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Exocrine_pancreatic_insufficiency|Limb_undergrowth|Macrocephaly|Motor_delay|Hypertelorism|Short_stature|Large_forehead|Disproportionate_short_stature": 1,
    "Wilms_tumor_susceptibility": 1,
    "Predisposition_to_Wilms_tumor": 21,
    "Predisposition_to_Wilms_tumor|not_provided": 6,
    "not_specified|CTR9-related_neurodevelopmental_disorder|not_provided": 1,
    "Predisposition_to_Wilms_tumor|Inborn_genetic_diseases": 1,
    "not_provided|CTR9-related_disorder": 6,
    "not_provided|CTR9-related_neurodevelopmental_disorder|Predisposition_to_Wilms_tumor|CTR9-related_disorder": 1,
    "CTR9-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Predisposition_to_Wilms_tumor|_CTR9-related|not_provided": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified": 4,
    "not_provided|TEAD1-related_disorder": 1,
    "TEAD1-related_disorder|not_provided": 3,
    "TEAD1-related_disorder": 2,
    "not_provided|Helicoid_peripapillary_chorioretinal_degeneration": 1,
    "not_provided|Helicoid_peripapillary_chorioretinal_degeneration|not_specified": 1,
    "Helicoid_peripapillary_chorioretinal_degeneration|Inborn_genetic_diseases": 1,
    "Primary_hyperparathyroidism|Familial_hypoparathyroidism": 1,
    "not_provided|not_specified|Familial_hypoparathyroidism|Hypoparathyroidism|_familial_isolated_1": 1,
    "Hypoparathyroidism|_familial_isolated_1|not_provided": 1,
    "Hypoparathyroidism|_familial_isolated_1": 7,
    "Familial_hypoparathyroidism|not_specified|not_provided|Hypoparathyroidism|_familial_isolated_1": 1,
    "PTH-related_disorder": 1,
    "Fatty_acyl-CoA_reductase_1_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|Fatty_acyl-CoA_reductase_1_deficiency|FAR1-related_disorder|not_provided": 1,
    "Fatty_acyl-CoA_reductase_1_deficiency": 4,
    "not_provided|FAR1-related_disorder": 3,
    "FAR1-related_disorder|not_provided": 1,
    "not_provided|CATARACTS|_SPASTIC_PARAPARESIS|_AND_SPEECH_DELAY|Fatty_acyl-CoA_reductase_1_deficiency": 1,
    "CATARACTS|_SPASTIC_PARAPARESIS|_AND_SPEECH_DELAY": 1,
    "not_provided|FAR1-related_neurodevelopmental_disorder|CATARACTS|_SPASTIC_PARAPLEGIA|_AND_SPEECH_DELAY|CATARACTS|_SPASTIC_PARAPARESIS|_AND_SPEECH_DELAY": 1,
    "not_provided|CATARACTS|_SPASTIC_PARAPLEGIA|_AND_SPEECH_DELAY|CATARACTS|_SPASTIC_PARAPARESIS|_AND_SPEECH_DELAY": 1,
    "CATARACTS|_SPASTIC_PARAPLEGIA|_AND_SPEECH_DELAY|CATARACTS|_SPASTIC_PARAPARESIS|_AND_SPEECH_DELAY|not_provided": 1,
    "Fatty_acyl-CoA_reductase_1_deficiency|CATARACTS|_SPASTIC_PARAPARESIS|_AND_SPEECH_DELAY": 1,
    "Noonan_syndrome_12": 2,
    "RRAS2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|RRAS2-related_disorder|Noonan_syndrome_12": 1,
    "not_provided|Noonan_syndrome_12|RASopathy": 1,
    "RRAS2-related_disorder": 7,
    "Noonan_syndrome_12|Ovarian_neoplasm|Noonan_syndrome": 1,
    "RASopathy|RRAS2-related_disorder|Noonan_syndrome|Noonan_syndrome_12": 1,
    "not_provided|RRAS2-related_disorder": 1,
    "RRAS2-related_disorder|not_provided": 1,
    "Noonan_syndrome_12|not_provided|Inborn_genetic_diseases|Noonan_syndrome": 1,
    "Noonan_syndrome_12|not_provided": 2,
    "Noonan_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Noonan_syndrome_12|RRAS2-related_disorder": 1,
    "Baralle-Macken_syndrome": 2,
    "Short_stature|Failure_to_thrive|Skeletal_dysplasia|Delayed_speech_and_language_development": 1,
    "Baralle-Macken_syndrome|Intellectual_disability|_severe|Immunodeficiency|Microcephaly|Cataract": 1,
    "not_specified|Baralle-Macken_syndrome": 2,
    "Baralle-Macken_syndrome|Intellectual_disability|_severe|Microcephaly|Cataract": 1,
    "not_provided|Vitamin_D_hydroxylation-deficient_rickets|_type_1B": 14,
    "Vitamin_D_hydroxylation-deficient_rickets|_type_1B": 57,
    "Low_serum_calcitriol": 1,
    "Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_provided": 11,
    "not_specified|Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_provided": 1,
    "Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_specified": 5,
    "CYP2R1-related_disorder|not_provided": 1,
    "Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_specified|not_provided": 3,
    "not_provided|not_specified|Vitamin_D_hydroxylation-deficient_rickets|_type_1B": 2,
    "not_specified|not_provided|Vitamin_D_hydroxylation-deficient_rickets|_type_1B": 1,
    "CYP2R1-related_disorder|not_provided|Vitamin_D_hydroxylation-deficient_rickets|_type_1B": 1,
    "not_provided|Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_specified": 1,
    "CYP2R1-related_disorder|Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_provided": 1,
    "Vitamin_D_hydroxylation-deficient_rickets|_type_1B|not_provided|not_specified": 2,
    "CYP2R1-related_disorder|not_provided|Vitamin_D_hydroxylation-deficient_rickets|_type_1B|Vitamin_D-dependent_rickets|_type_1": 1,
    "Pulmonary_disease|_chronic_obstructive|_susceptibility_to|not_provided|not_specified": 1,
    "CYP2R1-related_disorder": 1,
    "Calcitonin_polymorphism": 1,
    "SOX6-related_disorder": 4,
    "Tolchin-Le_Caignec_syndrome": 28,
    "SOX6-related_disorder|not_provided": 5,
    "not_provided|SOX6-related_disorder": 4,
    "Tolchin-Le_Caignec_syndrome|not_provided": 2,
    "not_provided|Tolchin-Le_Caignec_syndrome": 4,
    "not_provided|Inborn_genetic_diseases|Tolchin-Le_Caignec_syndrome": 1,
    "Craniosynostosis_syndrome|Tolchin-Le_Caignec_syndrome": 1,
    "Tolchin-Le_Caignec_syndrome|Inborn_genetic_diseases": 1,
    "PLEKHA7-related_disorder": 37,
    "not_provided|PLEKHA7-related_disorder": 4,
    "Cleft_lip_with_or_without_cleft_palate": 26,
    "not_specified|PLEKHA7-related_disorder": 1,
    "PLEKHA7-related_disorder|not_provided": 1,
    "not_provided|Oculocerebrodental_syndrome": 3,
    "Oculocerebrodental_syndrome|not_provided": 3,
    "PIK3C2A-related_disorder|not_provided": 8,
    "Oculocerebrodental_syndrome": 6,
    "not_provided|PIK3C2A-related_disorder|Oculocerebrodental_syndrome": 1,
    "not_provided|PIK3C2A-related_disorder": 7,
    "PIK3C2A-related_disorder|not_specified|not_provided": 2,
    "Oculocerebrodental_syndrome|Short_stature": 1,
    "not_provided|Oculocerebrodental_syndrome|PIK3C2A-related_disorder": 2,
    "not_specified|not_provided|PIK3C2A-related_disorder": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2": 2,
    "Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3": 5,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_3": 2,
    "Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 13,
    "Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_13": 2,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young": 4,
    "Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|not_provided|Diabetes_mellitus|_transient_neonatal|_3": 2,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 2,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young": 2,
    "Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_13|Neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|not_specified": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus_1|not_specified|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided|Hyperinsulinemia|not_specified|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus": 4,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus": 18,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young": 3,
    "Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|not_specified": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_13|Inborn_genetic_diseases|not_specified|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|not_specified|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus_1|not_provided": 1,
    "KCNJ11-related_disorder": 5,
    "Hyperinsulinemic_hypoglycemia|_familial|_2": 3,
    "Maturity-onset_diabetes_of_the_young_type_13|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_2|Inborn_genetic_diseases|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus": 1,
    "not_provided|not_specified|KCNJ11-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1": 8,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2|Monogenic_diabetes": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Monogenic_diabetes|not_provided|Permanent_neonatal_diabetes_mellitus|Inborn_genetic_diseases|not_specified|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|KCNJ11-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus": 3,
    "Neonatal_hypoglycemia|Permanent_neonatal_diabetes_mellitus": 2,
    "not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Neonatal_insulin-dependent_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_13": 3,
    "Inborn_genetic_diseases|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|not_specified|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus_1|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus_1|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|KCNJ11-related_disorder|Inborn_genetic_diseases": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Permanent_neonatal_diabetes_mellitus_1|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "sulfonylureas_response|Permanent_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemia|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Permanent_neonatal_diabetes_mellitus": 3,
    "Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|not_provided|Familial_hyperinsulinism|Hyperinsulinemia": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|KCNJ11-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Inborn_genetic_diseases|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|not_provided|not_specified": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Permanent_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Hyperinsulinemia|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided": 3,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|not_provided": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_13|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Diabetes_mellitus|_transient_neonatal|_3": 2,
    "Hyperinsulinemic_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus": 1,
    "KCNJ11-related_disorder|Hyperinsulinemia|Monogenic_diabetes": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|KCNJ11-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|not_provided|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Hereditary_ataxia|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus": 1,
    "not_specified|KCNJ11-related_disorder|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|not_provided|Type_2_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Inborn_genetic_diseases|Maturity-onset_diabetes_of_the_young_type_13|not_specified": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|not_provided|Hyperinsulinemia|Permanent_neonatal_diabetes_mellitus_1|Inborn_genetic_diseases": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus": 2,
    "Type_2_diabetes_mellitus|KCNJ11-related_disorder": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus_1|Hypoglycemia": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided": 1,
    "not_provided|Familial_hyperinsulinism|KCNJ11-related_disorder": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemia|Neonatal_insulin-dependent_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|not_provided|Neonatal_diabetes_mellitus": 1,
    "Diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|not_provided|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus": 1,
    "KCNJ11-related_disorder|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "Permanent_neonatal_diabetes_mellitus|not_provided|not_specified|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Permanent_neonatal_diabetes_mellitus|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Neonatal_hypoglycemia|Neonatal_insulin-dependent_diabetes_mellitus": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_13|KCNJ11-related_disorder|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "not_provided|Neonatal_hypoglycemia": 1,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_permanent_neonatal_2": 2,
    "Glibenclamide_response|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Hypoglycemia|Hyperinsulinemia": 1,
    "Diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity_onset_diabetes_mellitus_in_young|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3": 1,
    "not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus": 1,
    "KCNJ11-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Familial_hyperinsulinism|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|not_specified|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "not_provided|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3": 1,
    "Maturity_onset_diabetes_mellitus_in_young|DEND_syndrome": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Permanent_neonatal_diabetes_mellitus|Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant|not_provided|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 3,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "not_provided|Familial_hyperinsulinism|KCNJ11-related_disorder|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemia|Atopic_eczema|Hypoglycemia|Hypertrichosis": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemia": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Neonatal_diabetes_mellitus|Neonatal_insulin-dependent_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided|Hyperinsulinemic_hypoglycemia|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Neonatal_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_2|Permanent_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|KCNJ11-related_disorder|Permanent_neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes|Diabetes_mellitus|_permanent_neonatal_2|not_provided|Neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|not_provided|Permanent_neonatal_diabetes_mellitus_1|KCNJ11-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided": 1,
    "Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Inborn_genetic_diseases|not_provided|not_specified|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Monogenic_diabetes|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus_1|not_provided|Familial_hyperinsulinism": 1,
    "Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|not_provided": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Permanent_neonatal_diabetes_mellitus|KCNJ11-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided|Permanent_neonatal_diabetes_mellitus_1|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus_1|Diabetes_mellitus|_transient_neonatal|_3|not_provided|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "KCNJ11-related_disorder|Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive|Maturity-onset_diabetes_of_the_young_type_13|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus_type_2|_susceptibility_to|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_3|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_2|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity-onset_diabetes_of_the_young_type_13": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus": 1,
    "not_provided|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Diabetes_mellitus|_transient_neonatal|_3|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_13|Diabetes_mellitus|_permanent_neonatal_2": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_2|Maturity-onset_diabetes_of_the_young_type_13|not_provided|Permanent_neonatal_diabetes_mellitus_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_2|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_transient_neonatal|_3|Permanent_neonatal_diabetes_mellitus|Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant|Maturity-onset_diabetes_of_the_young_type_13|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Permanent_neonatal_diabetes_mellitus|KCNJ11-related_disorder|Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant|Maturity-onset_diabetes_of_the_young_type_13|not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_3|Hyperinsulinemic_hypoglycemia|_familial|_2": 1,
    "Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive|Maturity-onset_diabetes_of_the_young_type_13|Hyperinsulinemic_hypoglycemia|_familial|_2|Permanent_neonatal_diabetes_mellitus|not_specified|Diabetes_mellitus|_transient_neonatal|_3|Diabetes_mellitus|_permanent_neonatal_2|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|KCNJ11-related_disorder": 1,
    "Permanent_neonatal_diabetes_mellitus|Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 4,
    "Transitory_neonatal_diabetes_mellitus|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|Inborn_genetic_diseases|Hyperinsulinemic_hypoglycemia|_familial|_1|Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive": 1,
    "not_specified|Transient_Neonatal_Diabetes|_Dominant|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hereditary_hyperinsulinism|Neonatal_hypoglycemia|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Hyperinsulinism|_Dominant/Recessive": 1,
    "Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|not_provided|Maturity_onset_diabetes_mellitus_in_young": 3,
    "Hereditary_hyperinsulinism": 100,
    "Leucine-induced_hypoglycemia|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 105,
    "ABCC8-related_disorder": 24,
    "Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 4,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 2,
    "not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1": 7,
    "not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 13,
    "not_provided|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Inborn_genetic_diseases": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus": 15,
    "Hyperinsulinemic_hypoglycemia|_familial|_1": 94,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Inborn_genetic_diseases|not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "ABCC8-related_disorder|Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided": 1,
    "not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "ABCC8-related_disorder|Neonatal_diabetes_mellitus|Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 26,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Diabetes_mellitus|_permanent_neonatal_3|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young": 7,
    "not_provided|Hereditary_hyperinsulinism": 20,
    "Type_2_diabetes_mellitus|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 10,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|not_specified": 2,
    "Hereditary_hyperinsulinism|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_provided|Hereditary_hyperinsulinism|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 3,
    "Monogenic_diabetes|not_specified|Type_2_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|ABCC8-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus": 2,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 24,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 9,
    "not_specified|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 3,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|not_provided|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_specified|Permanent_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 12,
    "Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 5,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified": 6,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Type_2_diabetes_mellitus": 2,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 3,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1": 14,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus|not_specified|Inborn_genetic_diseases": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 18,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 7,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young": 3,
    "not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Autosomal_dominant_hyperinsulinism_due_to_SUR1_deficiency|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Inborn_genetic_diseases|not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 4,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hereditary_hyperinsulinism|not_provided|Familial_hyperinsulinism|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hereditary_hyperinsulinism|ABCC8-related_disorder|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "ABCC8-related_disorder|Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|not_provided|Transitory_neonatal_diabetes_mellitus|not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus|not_specified": 3,
    "Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 15,
    "ABCC8-related_disorder|not_provided": 5,
    "not_provided|Type_2_diabetes_mellitus|Neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_specified|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 2,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|not_specified|not_provided|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus": 2,
    "not_provided|ABCC8-related_disorder": 3,
    "Hereditary_hyperinsulinism|not_provided|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "not_provided|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|Familial_hyperinsulinism": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 5,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided": 18,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 3,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided": 3,
    "not_provided|Familial_hyperinsulinism": 2,
    "Diabetes_mellitus|_transient_neonatal|_2|not_provided|Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus": 1,
    "not_provided|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|not_provided|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 11,
    "Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided|not_specified": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Familial_hyperinsulinism|not_provided": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Type_2_diabetes_mellitus|not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young": 5,
    "Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|ABCC8-related_disorder|Hereditary_hyperinsulinism|not_provided|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 3,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 7,
    "not_specified|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|Inborn_genetic_diseases": 1,
    "MATURITY-ONSET_DIABETES_OF_THE_YOUNG|_TYPE_12|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|ABCC8-related_disorder|Monogenic_diabetes|not_provided": 1,
    "Monogenic_diabetes|ABCC8-related_disorder|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Monogenic_diabetes|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified|not_provided": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|not_provided|not_specified": 1,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|not_provided|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|not_provided|Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|ABCC8-related_disorder": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hereditary_hyperinsulinism|Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive|not_specified|not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 3,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|ABCC8-related_disorder|not_provided|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|ABCC8-related_disorder|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|not_specified|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Monogenic_diabetes": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|ABCC8-related_disorder|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Inborn_genetic_diseases|Familial_hyperinsulinism|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_specified|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided": 2,
    "ABCC8-related_disorder|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 4,
    "Transitory_neonatal_diabetes_mellitus|not_specified|not_provided|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Monogenic_diabetes|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hereditary_hyperinsulinism|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_specified": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hereditary_hyperinsulinism|ABCC8-related_disorder|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 2,
    "Hereditary_hyperinsulinism|not_provided": 18,
    "not_provided|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Monogenic_diabetes|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus|Familial_hyperinsulinism|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus|not_provided|not_specified|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Permanent_neonatal_diabetes_mellitus|ABCC8-related_disorder|Inborn_genetic_diseases|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_provided|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Diabetes_mellitus|_permanent_neonatal_3|Hereditary_hyperinsulinism|Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "ABCC8-related_disorder|Neonatal_diabetes_mellitus|not_provided": 1,
    "Inborn_genetic_diseases|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 6,
    "Hereditary_hyperinsulinism|not_provided|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|Transitory_neonatal_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|Familial_hyperinsulinism|not_provided|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Hypoglycemia|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Type_2_diabetes_mellitus|Hereditary_hyperinsulinism|not_provided|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Inborn_genetic_diseases": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism": 2,
    "Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|ABCC8-related_disorder|Hereditary_hyperinsulinism|not_specified|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_provided|Familial_hyperinsulinism": 1,
    "Hereditary_hyperinsulinism|Type_2_diabetes_mellitus|not_provided|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus": 2,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hereditary_hyperinsulinism|Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Neonatal_diabetes_mellitus": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided": 1,
    "not_provided|Type_2_diabetes_mellitus|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 2,
    "not_provided|Hereditary_hyperinsulinism|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_specified": 2,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_provided|Neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|MATURITY-ONSET_DIABETES_OF_THE_YOUNG|_TYPE_12|ABCC8-related_disorder|Familial_hyperinsulinism|Neonatal_diabetes_mellitus": 1,
    "Macrocephaly|Neonatal_respiratory_distress|Congestive_heart_failure|Short_stature|Growth_delay|Gastroesophageal_reflux|Feeding_difficulties|Small_for_gestational_age|Macrotia|Atrial_septal_defect|Cardiac_shunt|Hypoglycemia|Monogenic_diabetes|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus": 1,
    "ABCC8-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Inborn_genetic_diseases": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Hereditary_hyperinsulinism|not_provided|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism": 1,
    "ABCC8-related_disorder|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia": 1,
    "Hereditary_hyperinsulinism|Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_provided|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Leucine-induced_hypoglycemia": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Familial_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|ABCC8-related_disorder|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases|not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "not_specified|not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Familial_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|not_provided": 5,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "ABCC8-related_disorder|not_provided|Hereditary_hyperinsulinism": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 1,
    "Hereditary_hyperinsulinism|not_specified|Inborn_genetic_diseases|not_provided|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|not_specified|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|not_specified|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Pulmonary_arterial_hypertension|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism": 4,
    "Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided": 2,
    "not_provided|ABCC8-related_disorder|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|ABCC8-related_disorder|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism": 2,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "ABCC8-related_disorder|not_provided|Hereditary_hyperinsulinism|Inborn_genetic_diseases|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Leucine-induced_hypoglycemia": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|not_specified|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|not_provided": 1,
    "Hereditary_hyperinsulinism|Monogenic_diabetes|not_provided|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Inborn_genetic_diseases|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Neonatal_diabetes_mellitus|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Familial_hyperinsulinism": 1,
    "not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|not_specified|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Transitory_neonatal_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 3,
    "Familial_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Type_2_diabetes_mellitus": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|ABCC8-related_disorder|not_provided|Familial_hyperinsulinism": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Monogenic_diabetes|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|not_specified|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Hereditary_hyperinsulinism|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Familial_hyperinsulinism|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Pulmonary_arterial_hypertension|ABCC8-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_2|not_specified|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Maturity_onset_diabetes_mellitus_in_young|not_provided|Familial_hyperinsulinism|Neonatal_diabetes_mellitus": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Neonatal_diabetes_mellitus|Familial_hyperinsulinism|Type_2_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_specified|not_provided": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|not_provided|Neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|not_specified|Neonatal_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_specified|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 4,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism": 2,
    "not_provided|not_specified|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1": 3,
    "Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism": 1,
    "MATURITY-ONSET_DIABETES_OF_THE_YOUNG|_TYPE_12": 2,
    "not_provided|ABCC8-related_disorder|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Inborn_genetic_diseases|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 3,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Familial_hyperinsulinism": 2,
    "Hereditary_hyperinsulinism|Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus|not_specified|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|ABCC8-related_disorder|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|not_specified|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Familial_hyperinsulinism": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 2,
    "Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|ABCC8-related_disorder|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Permanent_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Neonatal_diabetes_mellitus": 1,
    "not_provided|Inborn_genetic_diseases|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Permanent_neonatal_diabetes_mellitus|not_specified|Pulmonary_arterial_hypertension": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Neonatal_diabetes_mellitus": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hereditary_hyperinsulinism|Inborn_genetic_diseases": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|ABCC8-related_disorder|Type_2_diabetes_mellitus|Familial_hyperinsulinism": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Hereditary_hyperinsulinism|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Neonatal_diabetes_mellitus": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified": 1,
    "Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "not_specified|ABCC8-related_disorder|not_provided": 1,
    "ABCC8-related_disorder|Diabetes_mellitus|_transient_neonatal|_2|not_specified|not_provided|Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_specified|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|Transitory_neonatal_diabetes_mellitus|not_provided": 2,
    "Pulmonary_arterial_hypertension|Inborn_genetic_diseases": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "Inborn_genetic_diseases|Leucine-induced_hypoglycemia|not_provided|Type_2_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "ABCC8-related_disorder|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hereditary_hyperinsulinism|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|not_specified": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Hereditary_hyperinsulinism|not_provided|Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Pulmonary_arterial_hypertension|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Transitory_neonatal_diabetes_mellitus|not_specified|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|ABCC8-related_disorder|Hereditary_hyperinsulinism|Inborn_genetic_diseases": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "Monogenic_diabetes|not_specified|not_provided|ABCC8-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Monogenic_diabetes|Hereditary_hyperinsulinism": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_provided|ABCC8-related_disorder|not_specified": 1,
    "Neonatal_respiratory_distress|Gastroesophageal_reflux|Congestive_heart_failure|Hypoglycemia|Feeding_difficulties|Macrotia|Short_stature|Atrial_septal_defect|Macrocephaly|Growth_delay|Small_for_gestational_age|Cardiac_shunt": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|ABCC8-related_disorder|not_provided|Familial_hyperinsulinism": 1,
    "Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|not_provided": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Inborn_genetic_diseases|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Cerebral_edema|not_specified|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|not_specified": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|not_provided": 1,
    "Hereditary_hyperinsulinism|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Neonatal_diabetes_mellitus|Familial_hyperinsulinism|Type_2_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified": 1,
    "not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Inborn_genetic_diseases|Type_2_diabetes_mellitus|Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_2_diabetes_mellitus|Neonatal_diabetes_mellitus|Familial_hyperinsulinism": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Familial_hyperinsulinism": 1,
    "Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|not_specified|Familial_hyperinsulinism|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Hereditary_hyperinsulinism|ABCC8-related_disorder": 1,
    "not_specified|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|not_provided": 1,
    "ABCC8-related_disorder|not_provided|not_specified": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_provided|Familial_hyperinsulinism": 1,
    "Transitory_neonatal_diabetes_mellitus|ABCC8-related_disorder|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|not_provided": 4,
    "not_specified|not_provided|Type_2_diabetes_mellitus|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus": 3,
    "Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|ABCC8-related_disorder|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_provided|Pulmonary_arterial_hypertension|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|not_specified|Type_2_diabetes_mellitus|Inborn_genetic_diseases|ABCC8-related_disorder": 1,
    "Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "Transient_Neonatal_Diabetes|_Dominant|Hyperinsulinism|_Dominant/Recessive|Inborn_genetic_diseases|not_specified|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus": 1,
    "not_provided|Type_2_diabetes_mellitus|See_cases|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Familial_hyperinsulinism|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus": 1,
    "Pulmonary_arterial_hypertension|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Hypoglycemia|Hereditary_hyperinsulinism|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_specified|Permanent_neonatal_diabetes_mellitus|not_provided|ABCC8-related_disorder": 1,
    "not_specified|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|ABCC8-related_disorder|not_specified": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_provided|See_cases|Familial_hyperinsulinism": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hereditary_hyperinsulinism|Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 2,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus": 1,
    "not_specified|Permanent_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism|Monogenic_diabetes|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Inborn_genetic_diseases|Permanent_neonatal_diabetes_mellitus|not_specified|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Pointed_chin|Bilateral_cryptorchidism|Hypoglycemia|Retrognathia|Polyhydramnios|Broad_forehead|Large_fleshy_ears|Triangular_face|Long_philtrum|Generalized_hypotonia|Neonatal_hypotonia|Large_for_gestational_age|Transitory_neonatal_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3": 2,
    "not_provided|not_specified|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Inborn_genetic_diseases|not_specified|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Hereditary_hyperinsulinism|Inborn_genetic_diseases|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Familial_hyperinsulinism|Pulmonary_arterial_hypertension|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Hereditary_hyperinsulinism|Inborn_genetic_diseases|not_specified|Transitory_neonatal_diabetes_mellitus": 1,
    "Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|ABCC8-related_disorder": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_provided|ABCC8-related_disorder|Familial_hyperinsulinism": 1,
    "not_provided|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Inborn_genetic_diseases": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_provided": 1,
    "not_provided|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_specified|Inborn_genetic_diseases|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hereditary_hyperinsulinism|Monogenic_diabetes|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified": 1,
    "Transitory_neonatal_diabetes_mellitus|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "Pulmonary_arterial_hypertension|not_provided|Inborn_genetic_diseases": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Permanent_neonatal_diabetes_mellitus": 1,
    "Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus": 1,
    "not_provided|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_specified": 1,
    "Type_2_diabetes_mellitus|Familial_hyperinsulinism|not_provided": 2,
    "not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Familial_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 2,
    "Permanent_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3": 1,
    "not_provided|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "not_specified|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 2,
    "Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hereditary_hyperinsulinism|not_provided": 1,
    "Transitory_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus": 1,
    "Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "ABCC8-related_disorder|Inborn_genetic_diseases|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism|Neonatal_diabetes_mellitus": 1,
    "not_specified|Hyperinsulinemic_hypoglycemia|_familial|_1|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus": 1,
    "Inborn_genetic_diseases|not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|not_specified|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|not_provided|Familial_hyperinsulinism": 1,
    "Neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus": 2,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|not_specified|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus": 2,
    "Diabetes_mellitus|_permanent_neonatal_3|Permanent_neonatal_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Permanent_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified": 1,
    "Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism|Type_2_diabetes_mellitus": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified": 1,
    "not_specified|Hereditary_hyperinsulinism": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|not_specified": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus|Hereditary_hyperinsulinism": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided|not_specified": 1,
    "not_specified|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|not_provided|Hereditary_disease": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified|not_provided": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|not_specified|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|Neonatal_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Monogenic_diabetes|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|not_specified": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 2,
    "Hereditary_hyperinsulinism|Inborn_genetic_diseases|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_specified|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Pulmonary_arterial_hypertension|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|not_provided|Familial_hyperinsulinism": 1,
    "Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Inborn_genetic_diseases|Hereditary_hyperinsulinism|not_specified|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Pulmonary_arterial_hypertension|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "Transitory_neonatal_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|not_specified|ABCC8-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Permanent_neonatal_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Inborn_genetic_diseases|Hereditary_hyperinsulinism": 1,
    "Hereditary_hyperinsulinism|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "ABCC8-related_disorder|not_specified|Monogenic_diabetes|Hyperinsulinemic_hypoglycemia|_familial|_1|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Permanent_neonatal_diabetes_mellitus|Familial_hyperinsulinism|not_provided": 1,
    "Familial_hyperinsulinism|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|ABCC8-related_disorder|not_provided": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|not_specified|Permanent_neonatal_diabetes_mellitus|Type_2_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|Neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "ABCC8-related_disorder|not_specified|not_provided|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "not_provided|Hyperinsulinemia|Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|not_specified|Diabetes_mellitus|_permanent_neonatal_3|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Permanent_neonatal_diabetes_mellitus": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hereditary_hyperinsulinism|not_provided": 1,
    "Permanent_neonatal_diabetes_mellitus|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_2_diabetes_mellitus|Hereditary_hyperinsulinism": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Neonatal_diabetes_mellitus": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_hyperinsulinism|Hyperinsulinemic_hypoglycemia|_familial|_1|Permanent_neonatal_diabetes_mellitus|ABCC8-related_disorder|Transitory_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Hereditary_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|not_provided|Transitory_neonatal_diabetes_mellitus": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hereditary_hyperinsulinism|Transitory_neonatal_diabetes_mellitus|Inborn_genetic_diseases": 1,
    "Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2": 1,
    "Congenital_isolated_hyperinsulinism|not_provided": 1,
    "Hereditary_hyperinsulinism|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|ABCC8-related_disorder|not_provided|Familial_hyperinsulinism": 1,
    "ABCC8-related_disorder|not_provided|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Diabetes_mellitus|_permanent_neonatal_3|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia": 1,
    "not_provided|Hyperinsulinemic_hypoglycemia|_familial|_1|Familial_hyperinsulinism|ABCC8-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Inborn_genetic_diseases|Transitory_neonatal_diabetes_mellitus": 1,
    "ABCC8-related_disorder|Hereditary_hyperinsulinism|Diabetes_mellitus|_transient_neonatal|_2|Type_2_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1|Leucine-induced_hypoglycemia|Diabetes_mellitus|_permanent_neonatal_3|not_provided": 1,
    "Hyperinsulinemic_hypoglycemia|_familial|_1|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Permanent_neonatal_diabetes_mellitus|not_specified": 1,
    "Permanent_neonatal_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus|_transient_neonatal|_2|not_provided|Transitory_neonatal_diabetes_mellitus|Hyperinsulinemic_hypoglycemia|_familial|_1": 1,
    "not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Permanent_neonatal_diabetes_mellitus|Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant": 1,
    "Permanent_neonatal_diabetes_mellitus|Hyperinsulinism|_Dominant/Recessive|Transient_Neonatal_Diabetes|_Dominant": 1,
    "ABCC8-related_disorder|Diabetes_mellitus|_permanent_neonatal_3|Type_2_diabetes_mellitus|Diabetes_mellitus|_transient_neonatal|_2|Leucine-induced_hypoglycemia|Hyperinsulinemic_hypoglycemia|_familial|_1|Transitory_neonatal_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Usher_syndrome_type_1C": 73,
    "Usher_syndrome_type_1C|not_provided": 28,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_provided": 13,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 17,
    "not_specified|not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 6,
    "not_provided|Usher_syndrome_type_1C": 39,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 29,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 17,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided": 16,
    "not_specified|Usher_syndrome_type_1C|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 3,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_provided": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|USH1C-related_disorder|not_provided": 1,
    "USH1C-related_disorder|not_specified|not_provided": 1,
    "not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified|Usher_syndrome_type_1C|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A": 37,
    "not_provided|Usher_syndrome_type_1C|Inborn_genetic_diseases": 1,
    "USH1C-related_disorder": 7,
    "USH1C-related_disorder|not_provided": 4,
    "not_provided|not_specified|Usher_syndrome_type_1C": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified|Usher_syndrome_type_1C": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_specified": 3,
    "not_specified|not_provided|Usher_syndrome_type_1C": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Usher_syndrome_type_1C|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 6,
    "Usher_syndrome_type_1C|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1C|USH1C-related_disorder|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 4,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified": 1,
    "not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1C|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1C": 6,
    "Usher_syndrome_type_1C|not_specified|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "USH1C-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_provided": 1,
    "not_provided|Usher_syndrome_type_1C|not_specified": 6,
    "not_specified|not_provided|Usher_syndrome_type_1C|Inborn_genetic_diseases": 2,
    "not_specified|Usher_syndrome_type_1C|not_provided": 4,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|not_provided": 3,
    "not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome": 1,
    "Usher_syndrome_type_1C|Inborn_genetic_diseases|USH1C-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_provided|not_specified": 4,
    "not_specified|not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Hearing_impairment": 1,
    "Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified": 1,
    "not_provided|USH1C-related_disorder|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|not_specified": 1,
    "Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1C|not_provided|USH1C-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_specified": 3,
    "Retinal_dystrophy|Meniere_disease|Optic_atrophy|Usher_syndrome_type_1|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|Usher_syndrome_type_1C": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Usher_syndrome_type_1|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|not_specified|Usher_syndrome_type_1C": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|not_specified": 2,
    "not_specified|Usher_syndrome_type_1C": 3,
    "USH1C-related_disorder|not_provided|not_specified": 1,
    "Usher_syndrome_type_1C|not_specified": 1,
    "Usher_syndrome_type_1C|not_provided|not_specified": 4,
    "Usher_syndrome_type_1C|Inborn_genetic_diseases|not_provided": 2,
    "USH1C-related_disorder|not_provided|Usher_syndrome_type_1C|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided": 9,
    "Retinitis_pigmentosa|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1C|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|Usher_syndrome_type_1C|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "Usher_syndrome_type_1C|not_specified|not_provided": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified|not_provided|Usher_syndrome_type_1C": 1,
    "Usher_syndrome_type_1C|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1": 2,
    "not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|USH1C-related_disorder": 1,
    "not_specified|not_provided|Usher_syndrome_type_1C|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "Usher_syndrome_type_1C|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Usher_syndrome_type_1C|USH1C-related_disorder": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_2|not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "Usher_syndrome_type_1C|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1C": 1,
    "not_provided|USH1C-related_disorder|Usher_syndrome_type_1C": 4,
    "not_provided|Usher_syndrome|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "not_provided|Usher_syndrome_type_1C|USH1C-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|Usher_syndrome_type_1C|not_provided": 2,
    "Hearing_impairment|USH1C-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1C|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Usher_syndrome_type_2|not_provided|Hearing_impairment": 1,
    "not_specified|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|Retinal_dystrophy|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_specified|not_provided": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1C": 1,
    "USH1C-related_disorder|not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "Usher_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "not_specified|Inborn_genetic_diseases|Usher_syndrome_type_1C|not_provided": 2,
    "Usher_syndrome_type_1C|not_provided|not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "not_provided|USH1C-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|Usher_syndrome_type_1C": 1,
    "Usher_syndrome_type_1C|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_provided|Usher_syndrome_type_1": 1,
    "USH1C-related_disorder|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1C": 1,
    "not_provided|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_specified": 1,
    "not_specified|Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A": 1,
    "Usher_syndrome_type_1C|USH1C-related_disorder|Rare_genetic_deafness|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1": 1,
    "USH1C-related_disorder|Rare_genetic_deafness|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C|not_provided|Usher_syndrome": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1C": 1,
    "Usher_syndrome_type_1C|Autosomal_recessive_nonsyndromic_hearing_loss_18A|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B": 40,
    "not_specified|not_provided|OTOG-related_disorder": 12,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_specified": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided": 20,
    "not_provided|not_specified|OTOG-related_disorder": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|OTOG-related_disorder|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|Rare_genetic_deafness": 1,
    "not_specified|Meniere_disease|OTOG-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|Hearing_impairment|not_specified|not_provided": 1,
    "not_provided|OTOG-related_disorder": 19,
    "OTOG-related_disorder": 20,
    "not_specified|OTOG-related_disorder|not_provided": 4,
    "OTOG-related_disorder|not_provided": 18,
    "not_specified|not_provided|OTOG-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "OTOG-related_disorder|not_specified|not_provided": 12,
    "not_specified|Meniere_disease|OTOG-related_disorder|not_provided": 1,
    "OTOG-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "not_provided|OTOG-related_disorder|not_specified": 3,
    "OTOG-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B|OTOG-related_disorder": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 10,
    "OTOG-related_disorder|not_provided|not_specified": 10,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided|not_specified": 4,
    "Autosomal_recessive_disease|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided|Rare_genetic_deafness": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B|Seizure|Intellectual_disability|Rare_genetic_deafness": 1,
    "Meniere_disease|not_specified|not_provided": 6,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided": 6,
    "OTOG-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|OTOG-related_disorder|not_provided": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_specified|not_provided": 4,
    "OTOG-related_disorder|Meniere_disease|not_specified|not_provided": 1,
    "Autosomal_recessive_disease|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "OTOG-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "OTOG-related_disorder|Meniere_disease|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_specified": 1,
    "OTOG-related_disorder|Hearing_loss|not_specified|not_provided": 1,
    "OTOG-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_specified": 1,
    "OTOG-related_disorder|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_18B|not_provided": 2,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_18B": 1,
    "Meniere_disease|not_provided|not_specified": 2,
    "not_specified|not_provided|Meniere_disease": 1,
    "MYOD1-related_disorder": 3,
    "not_provided|Myopathy|_congenital|_with_diaphragmatic_defects|_respiratory_insufficiency|_and_dysmorphic_facies": 1,
    "MYOD1-related_disorder|not_provided": 3,
    "Myopathy|_congenital|_with_diaphragmatic_defects|_respiratory_insufficiency|_and_dysmorphic_facies": 5,
    "Arthrogryposis_multiplex_congenita|Autosomal_dominant_centronuclear_myopathy|Myopathy|_congenital|_with_diaphragmatic_defects|_respiratory_insufficiency|_and_dysmorphic_facies": 1,
    "not_provided|MYOD1-related_disorder": 2,
    "Progressive_myoclonic_epilepsy_type_7": 324,
    "Progressive_myoclonic_epilepsy_type_7|not_provided": 15,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_7|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_7": 13,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_7|not_provided": 2,
    "Progressive_myoclonic_epilepsy_type_7|Inborn_genetic_diseases": 16,
    "not_specified|Progressive_myoclonic_epilepsy_type_7": 5,
    "KCNC1-related_disorder": 3,
    "Progressive_myoclonic_epilepsy_type_7|not_specified": 1,
    "not_provided|Progressive_myoclonic_epilepsy_type_7": 19,
    "not_provided|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_7": 3,
    "not_provided|KCNC1-related_disorder|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy_type_7": 2,
    "Inborn_genetic_diseases|KCNC1-related_disorder|not_provided|Progressive_myoclonic_epilepsy_type_7": 1,
    "not_provided|Progressive_myoclonic_epilepsy_type_7|Inborn_genetic_diseases": 3,
    "Progressive_myoclonic_epilepsy_type_7|not_provided|KCNC1-related_disorder": 1,
    "not_provided|KCNC1-related_disorder|Progressive_myoclonic_epilepsy_type_7": 1,
    "Seizure|Progressive_myoclonic_epilepsy_type_7": 1,
    "Progressive_myoclonic_epilepsy_type_7|KCNC1-related_disorder": 3,
    "Progressive_myoclonic_epilepsy_type_7|not_provided|Inborn_genetic_diseases|KCNC1-related_disorder": 1,
    "Progressive_myoclonic_epilepsy_type_7|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|KCNC1-related_disorder|Progressive_myoclonic_epilepsy_type_7": 1,
    "KCNC1-related_disorder|Progressive_myoclonic_epilepsy_type_7": 2,
    "Progressive_myoclonic_epilepsy_type_7|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Abnormal_cerebral_morphology|Progressive_myoclonic_epilepsy_type_7": 1,
    "not_provided|KCNC1-related_disorder": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_7|Inborn_genetic_diseases": 1,
    "TPH1-related_disorder": 3,
    ".|not_provided|SAA1-related_disorder": 1,
    "Hermansky-Pudlak_syndrome_5": 65,
    "Hermansky-Pudlak_syndrome_5|not_provided": 29,
    "not_provided|Hermansky-Pudlak_syndrome_5": 16,
    "HPS5-related_disorder|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_5": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_5": 9,
    "HPS5-related_disorder|not_provided|Hermansky-Pudlak_syndrome_5": 1,
    "not_provided|Hermansky-Pudlak_syndrome_5|not_specified": 4,
    "not_provided|HPS5-related_disorder": 8,
    "Hermansky-Pudlak_syndrome_5|not_specified": 1,
    "HPS5-related_disorder": 3,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome_5": 3,
    "HPS5-related_disorder|not_provided|Hermansky-Pudlak_syndrome_5|not_specified": 1,
    "HPS5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_5": 2,
    "not_specified|Hermansky-Pudlak_syndrome_5|HPS5-related_disorder|not_provided": 1,
    "not_provided|Hermansky-Pudlak_syndrome_5|Hermansky-Pudlak_syndrome": 2,
    "not_provided|Hermansky-Pudlak_syndrome_5|HPS5-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_5": 3,
    "not_provided|Hermansky-Pudlak_syndrome_5|not_specified|HPS5-related_disorder": 2,
    "not_specified|HPS5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hermansky-Pudlak_syndrome_5|HPS5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_5|not_provided": 1,
    "Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_5|not_provided": 2,
    "Hermansky-Pudlak_syndrome_5|not_provided|not_specified": 1,
    "not_specified|Hermansky-Pudlak_syndrome_5|not_provided": 3,
    "Hermansky-Pudlak_syndrome_5|Inborn_genetic_diseases|not_provided": 2,
    "Hermansky-Pudlak_syndrome_5|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_5": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_5|HPS5-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Hermansky-Pudlak_syndrome_5": 1,
    "decreased_blood_alpha-hydroxyisovalerate_levels": 1,
    "not_provided|Hermansky-Pudlak_syndrome_5|Inborn_genetic_diseases": 1,
    "HPS5-related_disorder|Hermansky-Pudlak_syndrome|not_provided": 1,
    "not_provided|HPS5-related_disorder|not_specified": 1,
    "Hermansky-Pudlak_syndrome_5|Hermansky-Pudlak_syndrome|not_provided": 1,
    "HPS5-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hermansky-Pudlak_syndrome_5|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_provided|Hermansky-Pudlak_syndrome_5|HPS5-related_disorder|not_specified": 1,
    "HPS5-related_disorder|not_specified|not_provided|Hermansky-Pudlak_syndrome_5": 1,
    "not_provided|not_specified|HPS5-related_disorder": 1,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 148,
    "LDHA-related_disorder|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 1,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency|not_provided": 9,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 2,
    "not_specified|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 2,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 1,
    "not_specified|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency|not_provided": 3,
    "not_provided|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency|not_specified": 1,
    "not_provided|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 3,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency|LDHA-related_disorder|not_provided|not_specified": 1,
    "not_provided|LDHA-related_disorder|Glycogen_storage_disease_due_to_lactate_dehydrogenase_M-subunit_deficiency": 1,
    "LDHA-related_disorder": 1,
    "LDHA-related_disorder|not_specified": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 117,
    "not_provided|Hypertrophic_cardiomyopathy_12": 2,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12": 54,
    "Hypertrophic_cardiomyopathy_12": 16,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 22,
    "not_provided|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided": 2,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiovascular_phenotype": 21,
    "not_provided|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12": 8,
    "not_specified|CSRP3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype": 4,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 6,
    "not_provided|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_12|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1M|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|not_provided": 2,
    "not_specified|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 3,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided": 3,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided": 7,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided|not_specified|Cardiomyopathy|Prolonged_QT_interval|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified": 3,
    "not_specified|Cardiomyopathy|CSRP3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|not_provided|Cardiomyopathy|CSRP3-related_disorder|not_specified": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "Hypertrophic_cardiomyopathy_12|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1M|not_specified|not_provided|CSRP3-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|CSRP3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiovascular_phenotype|not_provided": 2,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "CSRP3-related_disorder": 1,
    "not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiovascular_phenotype": 2,
    "not_specified|Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|CSRP3-related_disorder|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|not_specified": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12": 1,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_provided": 1,
    "Hypertrophic_cardiomyopathy_12|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "not_provided|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|See_cases": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Hypertrophic_cardiomyopathy_1": 1,
    "Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M": 1,
    "not_provided|CSRP3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_12|Dilated_cardiomyopathy_1M|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12": 1,
    "Hypertrophic_cardiomyopathy_12|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Sudden_unexplained_death|Hypertrophic_cardiomyopathy|CSRP3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1M|Hypertrophic_cardiomyopathy_12|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_12": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy": 2,
    "NAV2-related_disorder|not_provided": 6,
    "NAV2-related_disorder": 34,
    "not_provided|NAV2-related_disorder": 6,
    "not_specified|NAV2-related_disorder": 2,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "NAV2-related_disorder|not_specified": 1,
    "NAV2-related_neurodevelopmental_condition": 2,
    "not_provided|Hyperekplexia": 4,
    "Hyperekplexia_3": 596,
    "not_provided|Hyperekplexia_3": 8,
    "Hyperekplexia_3|Inborn_genetic_diseases|not_provided|Hyperekplexia": 1,
    "Hyperekplexia_3|Inborn_genetic_diseases": 20,
    "Inborn_genetic_diseases|Hyperekplexia_3": 31,
    "Hyperekplexia_3|Hyperekplexia": 9,
    "Hyperekplexia_3|not_provided": 11,
    "Hyperekplexia_3|Inborn_genetic_diseases|Hyperekplexia": 4,
    "Hyperekplexia_3|not_provided|Hyperekplexia": 11,
    "Hyperekplexia_3|not_specified|not_provided|Hyperekplexia": 3,
    "Hyperekplexia_3|SLC6A5-related_disorder": 6,
    "not_provided|Hyperekplexia_3|Inborn_genetic_diseases": 3,
    "Hyperekplexia_3|SLC6A5-related_disorder|not_provided|Hyperekplexia": 3,
    "Inborn_genetic_diseases|Hyperekplexia_3|not_specified": 1,
    "SLC6A5-related_disorder": 4,
    "SLC6A5-related_disorder|Hyperekplexia_3": 1,
    "Exaggerated_startle_response": 1,
    "not_provided|Exaggerated_startle_response|Hyperekplexia_3": 1,
    "not_provided|Hyperekplexia_3|Hyperekplexia": 4,
    "Hyperekplexia_3|Hyperekplexia|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Hyperekplexia": 1,
    "Hyperekplexia_3|SLC6A5-related_disorder|not_provided": 1,
    "Hyperekplexia_3|SLC6A5-related_disorder|Hyperekplexia": 1,
    "Inborn_genetic_diseases|not_provided|Hyperekplexia_3": 1,
    "Hyperekplexia_3|not_provided|Hyperekplexia|not_specified": 1,
    "SLC6A5-related_disorder|Hyperekplexia_3|not_provided": 1,
    "not_provided|Hyperekplexia_3|SLC6A5-related_disorder|Hyperekplexia": 1,
    "not_provided|SLC6A5-related_disorder|Hyperekplexia": 1,
    "Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|not_provided|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "ANO5-Related_Muscle_Diseases": 18,
    "Limb-girdle_muscular_dystrophy|_recessive|ANO5-Related_Muscle_Diseases|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Gnathodiaphyseal_dysplasia": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases": 11,
    "Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive": 31,
    "Gnathodiaphyseal_dysplasia|Miyoshi_myopathy|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|ANO5-Related_Muscle_Diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-Related_Muscle_Diseases|Miyoshi_muscular_dystrophy_3|not_specified|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Miyoshi_myopathy": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 78,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 519,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 19,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 52,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Inborn_genetic_diseases": 15,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_provided": 34,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 111,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Inborn_genetic_diseases|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Inborn_genetic_diseases|ANO5-related_disorder": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|ANO5-Related_Muscle_Diseases|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_provided": 2,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "Gnathodiaphyseal_dysplasia|not_provided|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_3|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-Related_Muscle_Diseases|not_specified|not_provided": 3,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Miyoshi_muscular_dystrophy_3": 2,
    "ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_3|not_provided|Abnormality_of_the_musculature": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|ANO5-Related_Muscle_Diseases": 2,
    "not_specified|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 6,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 5,
    "ANO5-related_disorder|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 3,
    "ANO5-related_muscular_dystrophy|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Polycystic_kidney_disease|Elevated_circulating_creatine_kinase_concentration|Lower_limb_amyotrophy|Achilles_tendon_contracture|Lower_limb_muscle_weakness|ANO5-related_disorder|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Myopathy|Intellectual_disability": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Inborn_genetic_diseases|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified": 3,
    "not_specified|not_provided|ANO5-Related_Muscle_Diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3": 1,
    "not_specified|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-Related_Muscle_Diseases|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 7,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_specified": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_3|Abnormality_of_the_musculature|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|not_specified|Miyoshi_muscular_dystrophy_3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|not_provided": 2,
    "Limb-girdle_muscular_dystrophy|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3": 3,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Intellectual_disability": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Inborn_genetic_diseases": 4,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-Related_Muscle_Diseases|not_specified|not_provided|Miyoshi_muscular_dystrophy_3": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-related_disorder|ANO5-Related_Muscle_Diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_3|not_specified|not_provided": 1,
    "ANO5-Related_Muscle_Diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "ANO5-related_disorder|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified|not_provided": 3,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Miyoshi_muscular_dystrophy_3": 2,
    "ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy|Miyoshi_muscular_dystrophy_3|not_provided|Hereditary_fructosuria": 1,
    "not_specified|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Elevated_circulating_creatine_kinase_concentration": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "ANO5-Related_Muscle_Diseases|not_specified|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 1,
    "ANO5-Related_Muscle_Diseases|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|not_specified|Miyoshi_muscular_dystrophy_3": 1,
    "Inborn_genetic_diseases|not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 2,
    "ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Gnathodiaphyseal_dysplasia": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_provided": 1,
    "Gnathodiaphyseal_dysplasia": 6,
    "not_provided|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified|Gnathodiaphyseal_dysplasia": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_provided|Miyoshi_muscular_dystrophy_3": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Limb-girdle_muscular_dystrophy|_recessive|ANO5-Related_Muscle_Diseases|Miyoshi_myopathy|not_specified|not_provided|Miyoshi_muscular_dystrophy_3": 1,
    "not_provided|ANO5-Related_Muscle_Diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy": 1,
    "ANO5-related_disorder": 4,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "Gnathodiaphyseal_dysplasia|not_provided": 2,
    "not_provided|Gnathodiaphyseal_dysplasia|ANO5-Related_Muscle_Diseases|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 4,
    "not_specified|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Muscular_dystrophy|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Autosomal_recessive_limb-girdle_muscular_dystrophy": 2,
    "not_specified|not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Miyoshi_muscular_dystrophy_3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-related_disorder": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|ANO5-related_disorder": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-Related_Muscle_Diseases|Myopathy": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Inborn_genetic_diseases|ANO5-related_disorder|not_specified": 1,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3": 1,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-Related_Muscle_Diseases|Intellectual_disability": 1,
    "Gnathodiaphyseal_dysplasia|not_specified|not_provided|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Inborn_genetic_diseases|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 1,
    "Inborn_genetic_diseases|ANO5-Related_Muscle_Diseases": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-Related_Muscle_Diseases|Muscular_dystrophy|Miyoshi_muscular_dystrophy_3|Myopathy|Distal_muscle_weakness|Elevated_circulating_creatine_kinase_concentration|Fatty_replacement_of_skeletal_muscle|not_provided": 1,
    "Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Inborn_genetic_diseases": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|not_provided|Abnormality_of_the_musculature": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "ANO5-Related_Muscle_Diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy|ANO5-Related_Muscle_Diseases|not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_myopathy": 1,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Elevated_circulating_creatine_kinase_concentration|Fatty_replacement_of_skeletal_muscle|Distal_muscle_weakness|Miyoshi_muscular_dystrophy_3": 1,
    "Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified": 1,
    "Myopathy|Gnathodiaphyseal_dysplasia": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Myopathy|not_provided": 1,
    "Miyoshi_muscular_dystrophy_3": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Miyoshi_muscular_dystrophy_3|not_specified|not_provided": 1,
    "ANO5-Related_Muscle_Diseases|not_specified|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "not_provided|ANO5-related_disorder|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Miyoshi_muscular_dystrophy_3|not_specified": 1,
    "not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_specified|Miyoshi_muscular_dystrophy_3": 2,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|not_specified": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia|not_provided": 1,
    "not_specified|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|ANO5-Related_Muscle_Diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_specified|ANO5-Related_Muscle_Diseases": 1,
    "ANO5_Muscle_Disease|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Miyoshi_muscular_dystrophy_3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-related_disorder|ANO5-Related_Muscle_Diseases|Miyoshi_muscular_dystrophy_3|not_provided|not_specified": 1,
    "Miyoshi_muscular_dystrophy_3|not_provided|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|ANO5-related_disorder|not_provided": 1,
    "Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|not_provided|ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Miyoshi_muscular_dystrophy_3|not_provided": 1,
    "not_specified|ANO5-Related_Muscle_Diseases|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|not_provided": 1,
    "not_provided|not_specified|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|Miyoshi_muscular_dystrophy_3|ANO5-Related_Muscle_Diseases|not_specified|not_provided": 1,
    "not_specified|Miyoshi_myopathy|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Limb-girdle_muscular_dystrophy|_recessive|ANO5-Related_Muscle_Diseases|not_provided": 1,
    "ANO5-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia|ANO5-Related_Muscle_Diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|not_specified": 1,
    "ANO5-Related_Muscle_Diseases|not_provided": 9,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy": 3,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases": 1,
    "not_provided|ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "not_provided|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive": 6,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|not_provided": 2,
    "not_provided|ANO5-Related_Muscle_Diseases": 1,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 2,
    "Miyoshi_myopathy|ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 3,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|not_provided|Gnathodiaphyseal_dysplasia": 2,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|not_provided|Gnathodiaphyseal_dysplasia": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|not_provided": 1,
    "ANO5-Related_Muscle_Diseases|Gnathodiaphyseal_dysplasia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Miyoshi_muscular_dystrophy_3|not_provided": 1,
    "ANO5-Related_Muscle_Diseases|Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3|Gnathodiaphyseal_dysplasia|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Miyoshi_myopathy|Miyoshi_muscular_dystrophy_3|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2L|Gnathodiaphyseal_dysplasia": 1,
    "Fanconi_anemia_complementation_group_F": 87,
    "not_specified|Fanconi_anemia_complementation_group_F": 1,
    "not_provided|Fanconi_anemia_complementation_group_F": 5,
    "Fanconi_anemia_complementation_group_F|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_F": 23,
    "not_provided|Fanconi_anemia_complementation_group_F|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia_complementation_group_F|Fanconi_anemia": 33,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_F|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_F": 3,
    "Fanconi_anemia_complementation_group_F|Inborn_genetic_diseases": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_F": 2,
    "FANCF-related_disorder|Fanconi_anemia": 2,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_F": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_F": 1,
    "Fanconi_anemia_complementation_group_F|not_specified": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_F|Inborn_genetic_diseases": 1,
    "not_provided|Fanconi_anemia_complementation_group_F|Fanconi_anemia": 3,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_F|not_specified": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_F": 2,
    "Fanconi_anemia|FANCF-related_disorder": 2,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_F": 2,
    "Fanconi_anemia|not_provided|FANCF-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_F": 4,
    "FANCF-related_disorder": 2,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_F|not_provided": 1,
    "Fanconi_anemia_complementation_group_F|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_F|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_F|not_provided": 1,
    "Fanconi_anemia_complementation_group_F|FANCF-related_disorder|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_F|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Fanconi_anemia_complementation_group_F|Malignant_tumor_of_breast|Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "FANCF-related_disorder|not_provided|Fanconi_anemia_complementation_group_F|not_specified|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_F|not_specified|not_provided": 2,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_F": 3,
    "not_specified|Fanconi_anemia_complementation_group_F|Fanconi_anemia": 2,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_F|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia_complementation_group_F|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia|not_provided|not_specified|Fanconi_anemia_complementation_group_F": 1,
    "Fanconi_anemia|FANCF-related_disorder|not_specified|Fanconi_anemia_complementation_group_F": 1,
    "Fanconi_anemia|Ovarian_cancer|Fanconi_anemia_complementation_group_F|FANCF-related_disorder|not_specified": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_F|not_specified": 1,
    "Fanconi_anemia_complementation_group_F|not_provided|Fanconi_anemia": 3,
    "Fanconi_anemia_complementation_group_F|not_specified|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia|Hereditary_cancer|Fanconi_anemia_complementation_group_F": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_F|Fanconi_anemia": 1,
    "FANCF-related_disorder|not_provided|Fanconi_anemia": 1,
    "FANCF-related_disorder|Fanconi_anemia_complementation_group_F|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia_complementation_group_F|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_F|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_F|Fanconi_anemia|not_provided|not_specified": 1,
    "Hearing_loss|_autosomal_recessive_125": 2,
    "Dystonia_24|not_provided": 13,
    "Dystonia_24": 18,
    "not_provided|Dystonia_24": 5,
    "ANO3-related_disorder|Dystonic_disorder": 1,
    "Dystonic_disorder|Dystonia_24|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Dystonic_disorder|Dystonia_24|not_provided": 4,
    "ANO3-related_disorder": 2,
    "Inborn_genetic_diseases|ANO3-related_disorder": 1,
    "not_provided|Dystonic_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Dystonia_24|Dystonic_disorder": 4,
    "ANO3-related_disorder|not_provided|Dystonic_disorder|Dystonia_24": 1,
    "Dystonic_disorder|Dystonia_24": 5,
    "Dystonia_24|Dystonic_disorder|not_provided": 2,
    "Dystonia_24|not_provided|Dystonic_disorder": 5,
    "not_provided|Dystonic_disorder|Dystonia_24": 3,
    "Dystonia_24|ANO3-related_disorder|Dystonic_disorder": 1,
    "Dystonic_disorder|not_provided|Dystonia_24": 2,
    "ANO3-related_disorder|not_provided|Dystonia_24|Dystonic_disorder": 1,
    "Dystonic_disorder|ANO3-related_disorder": 1,
    "See_cases|not_provided|Dystonia_24": 1,
    "not_provided|Dystonia_24|Inborn_genetic_diseases": 1,
    "Dystonia_24|ANO3-related_disorder|not_provided|Dystonic_disorder": 1,
    "not_provided|ANO3-related_disorder|Dystonia_24|Dystonic_disorder": 1,
    "Dystonia_24|Dystonic_disorder": 2,
    "Dystonic_disorder|Hereditary_ataxia": 1,
    "Dystonic_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Dystonic_disorder|Dystonia_24": 1,
    "not_provided|Dystonic_disorder|ANO3-related_disorder": 1,
    "ANO3-related_disorder|Dystonic_disorder|not_provided|Dystonia_24": 1,
    "BBOX1-related_disorder": 1,
    "Spermatogenic_failure_76": 2,
    "LGR4-related_disorder": 5,
    "LGR4-related_disorder|not_provided": 1,
    "not_provided|Delayed_puberty|_self-limited": 1,
    "Bone_mineral_density_quantitative_trait_locus_17": 1,
    "BDNF-related_disorder": 77,
    "not_provided|BDNF-related_disorder": 4,
    "BDNF-related_disorder|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|BDNF-related_disorder": 1,
    "BDNF-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|BDNF-related_disorder": 2,
    "not_specified|not_provided|Memory_impairment|_susceptibility_to": 1,
    "BDNF-related_disorder|not_specified|not_provided|Obesity|Congenital_central_hypoventilation": 1,
    "not_provided|Microcephaly|_cataracts|_impaired_intellectual_development|_and_dystonia_with_abnormal_striatum": 1,
    "Microcephaly|_cataracts|_impaired_intellectual_development|_and_dystonia_with_abnormal_striatum": 3,
    "Hypogonadotropic_hypogonadism_24_without_anosmia": 20,
    "not_provided|FSHB-related_disorder|Hypogonadotropic_hypogonadism_24_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_24_without_anosmia|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism_24_without_anosmia|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_24_without_anosmia": 7,
    "FSHB-related_disorder": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_24_without_anosmia": 1,
    "Global_developmental_delay|Abnormal_facial_shape|Truncal_obesity|Microcephaly|not_provided": 1,
    "DCDC5-related_condition": 9,
    "DCDC5-related_condition|not_provided": 5,
    "DCDC1-related_disorder": 19,
    "DCDC1-related_disorder|not_provided": 2,
    "not_provided|DCDC1-related_disorder|Head_and_neck_cancer": 1,
    "not_provided|DCDC1-related_disorder": 1,
    "ELP4-related_disorder|not_provided": 2,
    "ELP4-related_disorder": 6,
    "Seizure|Cognitive_impairment|Global_developmental_delay": 1,
    "Global_developmental_delay|Seizure|Cognitive_impairment": 1,
    "Aniridia_2|not_provided": 1,
    "Aniridia_2": 1,
    "Aniridia_1": 160,
    "not_provided|ELP4-related_disorder|not_specified": 1,
    "not_provided|not_specified|ELP4-related_disorder": 1,
    "not_provided|Autosomal_dominant_keratitis|Congenital_aniridia|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Foveal_hypoplasia_1": 8,
    "Anophthalmia|Autosomal_dominant_keratitis|Congenital_aniridia|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Irido-corneo-trabecular_dysgenesis": 1,
    "Foveal_hypoplasia_1|Autosomal_dominant_keratitis|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome": 1,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Congenital_aniridia|11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Autosomal_dominant_keratitis|Congenital_aniridia|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 3,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis": 279,
    "Autosomal_dominant_keratitis|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis": 7,
    "Autosomal_dominant_keratitis|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 3,
    "Congenital_aniridia|Autosomal_dominant_keratitis|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|not_provided|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Congenital_aniridia|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Aniridia_1|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia|Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Congenital_aniridia|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Anophthalmia|Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|Congenital_aniridia|Irido-corneo-trabecular_dysgenesis": 1,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome": 1,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Aniridia_1|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome": 1,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Congenital_aniridia|Anophthalmia|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis": 3,
    "not_provided|11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|not_provided|Foveal_hypoplasia_1|Aniridia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Congenital_aniridia|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|not_provided|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Congenital_aniridia|Foveal_hypoplasia_1|Anophthalmia-microphthalmia_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Congenital_aniridia|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Congenital_aniridia|Anophthalmia|not_provided|Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Irido-corneo-trabecular_dysgenesis": 1,
    "Anophthalmia|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Congenital_aniridia|Irido-corneo-trabecular_dysgenesis|11p_partial_monosomy_syndrome": 2,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Aniridia_1|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia|11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Congenital_aniridia|Irido-corneo-trabecular_dysgenesis": 2,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|Aniridia_1|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Congenital_aniridia|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Foveal_hypoplasia_1": 1,
    "Anophthalmia|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|Irido-corneo-trabecular_dysgenesis": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Aniridia_1|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Congenital_aniridia|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|Aniridia_1|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|not_provided|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Aniridia_1|Congenital_aniridia|Irido-corneo-trabecular_dysgenesis|not_provided|Foveal_hypoplasia_1|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Congenital_aniridia|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|Anophthalmia-microphthalmia_syndrome|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|not_provided|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia_1|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis": 1,
    "Congenital_aniridia|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|11p_partial_monosomy_syndrome|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|Congenital_aniridia|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|Aniridia_1|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Congenital_aniridia|Anophthalmia-microphthalmia_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Aniridia_1": 1,
    "carboxymethyl-dextran-A2-gadolinium-DOTA|11p_partial_monosomy_syndrome|Aniridia_1|not_provided|Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1": 1,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome|Aniridia_1|Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome": 1,
    "Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 3,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA|Aniridia_1|Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis": 1,
    "not_provided|Autosomal_dominant_keratitis|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia|not_provided|Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Irido-corneo-trabecular_dysgenesis": 1,
    "Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Autosomal_dominant_keratitis|carboxymethyl-dextran-A2-gadolinium-DOTA|not_provided|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1": 1,
    "Autosomal_dominant_keratitis|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1": 9,
    "Autosomal_dominant_keratitis|Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1|11p_partial_monosomy_syndrome|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Autosomal_dominant_keratitis|Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Autosomal_dominant_keratitis|Irido-corneo-trabecular_dysgenesis": 1,
    "not_provided|Coloboma_of_optic_nerve": 1,
    "not_provided|not_specified|Aniridia_1|11p_partial_monosomy_syndrome": 1,
    "Coloboma_of_optic_nerve|PAX6-related_ocular_dysgenesis|not_provided": 1,
    "PAX6-related_ocular_dysgenesis": 1,
    "Sporadic_aniridia|Visual_impairment|Nystagmus|Hypertelorism|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_ocular_coloboma|Irido-corneo-trabecular_dysgenesis|Autosomal_dominant_keratitis|Coloboma_of_optic_nerve|Aniridia_1|Isolated_optic_nerve_hypoplasia|not_provided": 1,
    "Coloboma_of_optic_nerve|not_specified": 1,
    "Aniridia_1|not_provided": 13,
    "Coloboma_of_optic_nerve": 2,
    "Irido-corneo-trabecular_dysgenesis|Aniridia_1|Inborn_genetic_diseases": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|PAX6-related_disorder": 4,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|Inborn_genetic_diseases": 4,
    "Foveal_hypoplasia_1|11p_partial_monosomy_syndrome|Aniridia_1|Coloboma|_ocular|_autosomal_dominant|Irido-corneo-trabecular_dysgenesis|Coloboma_of_optic_nerve|Autosomal_dominant_keratitis|Isolated_optic_nerve_hypoplasia": 1,
    "Optic_nerve_aplasia|_bilateral": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|Coloboma_of_optic_nerve": 1,
    "Irido-corneo-trabecular_dysgenesis|Aniridia_1": 48,
    "Aniridia_1|not_provided|Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1|Autosomal_dominant_keratitis|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA|Irido-corneo-trabecular_dysgenesis": 1,
    "not_provided|Irido-corneo-trabecular_dysgenesis|Aniridia_1": 5,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|not_specified": 1,
    "Inborn_genetic_diseases|Aniridia_1|Irido-corneo-trabecular_dysgenesis": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|not_provided": 13,
    "Aniridia_1|Developmental_cataract": 1,
    "Aniridia_1|Cataracts|_congenital|_with_late-onset_corneal_dystrophy": 1,
    "not_provided|Aniridia_1|Irido-corneo-trabecular_dysgenesis": 11,
    "Aniridia_1|not_provided|Irido-corneo-trabecular_dysgenesis": 3,
    "PAX6-related_disorder": 11,
    "Coloboma|_ocular|_autosomal_dominant": 7,
    "not_provided|PAX6-related_disorder|Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_specified": 1,
    "Congenital_aniridia": 6,
    "carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1": 1,
    "not_provided|Aniridia_1|Albinism_or_congenital_nystagmus|Irido-corneo-trabecular_dysgenesis": 1,
    "Foveal_hypoplasia_1|Autosomal_dominant_keratitis|Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_provided|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome": 1,
    "11p_partial_monosomy_syndrome|Aniridia_1|Irido-corneo-trabecular_dysgenesis|Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Autosomal_dominant_keratitis": 1,
    "PAX6-related_disorder|Aniridia_1|Irido-corneo-trabecular_dysgenesis": 2,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Aniridia_1|Irido-corneo-trabecular_dysgenesis|Foveal_hypoplasia_1|not_provided|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome": 1,
    "PAX6-related_disorder|Coloboma_of_optic_nerve|Isolated_optic_nerve_hypoplasia|11p_partial_monosomy_syndrome|Congenital_ocular_coloboma|Autosomal_dominant_keratitis|Irido-corneo-trabecular_dysgenesis|Aniridia_1|Foveal_hypoplasia_1|Coloboma|_ocular|_autosomal_dominant|not_provided": 1,
    "not_provided|Aniridia_1|11p_partial_monosomy_syndrome|Anophthalmia-microphthalmia_syndrome|Abnormality_of_refraction|Irido-corneo-trabecular_dysgenesis|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|not_specified|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|not_provided|Congenital_aniridia": 1,
    "not_provided|Aniridia_1": 7,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Aniridia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Irido-corneo-trabecular_dysgenesis|Autosomal_dominant_keratitis|not_provided|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|PAX6-related_disorder|Foveal_hypoplasia_1|not_provided": 1,
    "Irido-corneo-trabecular_dysgenesis|Aniridia_1|Isolated_optic_nerve_hypoplasia|not_provided": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|not_provided|Inborn_genetic_diseases": 1,
    "Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Autosomal_dominant_keratitis|carboxymethyl-dextran-A2-gadolinium-DOTA": 2,
    "Isolated_optic_nerve_hypoplasia|11p_partial_monosomy_syndrome|Aniridia_1|Coloboma|_ocular|_autosomal_dominant|Coloboma_of_optic_nerve|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Irido-corneo-trabecular_dysgenesis": 1,
    "not_provided|PAX6-related_disorder|Aniridia_1|Irido-corneo-trabecular_dysgenesis": 2,
    "Aniridia_1|Foveal_hypoplasia_1|Coloboma_of_optic_nerve|Autosomal_dominant_keratitis|Irido-corneo-trabecular_dysgenesis|Isolated_optic_nerve_hypoplasia|Coloboma|_ocular|_autosomal_dominant": 1,
    "Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_provided": 3,
    "not_provided|Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_specified": 1,
    "Aniridia_1|Foveal_hypoplasia_1|Irido-corneo-trabecular_dysgenesis": 1,
    "PAX6-related_ocular_dysgenesis|Irido-corneo-trabecular_dysgenesis|Aniridia_1|Aniridia|_atypical": 1,
    "Isolated_optic_nerve_hypoplasia|Developmental_disorder": 1,
    "not_specified|PAX6-related_disorder|Aniridia_1|Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "PAX6-related_disorder|Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_provided": 1,
    "not_specified|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Aniridia_1|Irido-corneo-trabecular_dysgenesis|not_provided|Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome": 1,
    "Aniridia_1|Irido-corneo-trabecular_dysgenesis|Autosomal_dominant_keratitis|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "11p_partial_monosomy_syndrome|not_provided": 1,
    "Intellectual_disability|Aniridia_1|Isolated_optic_nerve_hypoplasia|Foveal_hypoplasia_1|Irido-corneo-trabecular_dysgenesis|11p_partial_monosomy_syndrome|Coloboma|_ocular|_autosomal_dominant": 1,
    "Foveal_hypoplasia_1_with_cataract|Aniridia_1": 1,
    "Anterior_segment_dysgenesis|Irido-corneo-trabecular_dysgenesis": 1,
    "ANTERIOR_SEGMENT_DYSGENESIS_5|_MULTIPLE_SUBTYPES|Foveal_hypoplasia_1_with_or_without_anterior_segment_anomalies": 1,
    "PAX6-related_ocular_dysgenesis|not_provided|Iris_coloboma": 1,
    "Developmental_cataract|Microphthalmia": 1,
    "PAX6-related_disorder|Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_provided|not_specified": 1,
    "Coloboma|_ocular|_autosomal_dominant|Aniridia_1|Irido-corneo-trabecular_dysgenesis": 1,
    "Coloboma|_ocular|_autosomal_dominant|Irido-corneo-trabecular_dysgenesis|Aniridia_1": 1,
    "Foveal_hypoplasia_1|not_provided|Aniridia_1": 1,
    "Aniridia_1|Coloboma|_ocular|_autosomal_dominant": 1,
    "Aniridia_1|Coloboma|_ocular|_autosomal_dominant|ANTERIOR_SEGMENT_DYSGENESIS_5|_PETERS_ANOMALY_SUBTYPE": 1,
    "Irido-corneo-trabecular_dysgenesis|Aniridia_1|not_provided|PAX6-related_disorder": 1,
    "Foveal_hypoplasia_1": 1,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|not_provided|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Aniridia_1|11p_partial_monosomy_syndrome|Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1": 1,
    "Aniridia_1|not_specified": 1,
    "Isolated_anophthalmia-microphthalmia_syndrome|Aniridia_1|Irido-corneo-trabecular_dysgenesis": 1,
    "Anophthalmia-microphthalmia_syndrome|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA|Irido-corneo-trabecular_dysgenesis|Aniridia_1|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|not_specified|Congenital_aniridia|not_provided": 1,
    "Aniridia_1|PAX6-related_disorder": 1,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA|Autosomal_dominant_keratitis|Foveal_hypoplasia_1|Anophthalmia-microphthalmia_syndrome|Aniridia_1": 1,
    "Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Foveal_hypoplasia_1|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA|Anophthalmia-microphthalmia_syndrome|Autosomal_dominant_keratitis|Aniridia_1": 1,
    "Autosomal_dominant_keratitis|Anophthalmia-microphthalmia_syndrome|not_provided|11p_partial_monosomy_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia-microphthalmia_syndrome|Foveal_hypoplasia_1|Congenital_aniridia|Autosomal_dominant_keratitis|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|11p_partial_monosomy_syndrome|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Anophthalmia|Foveal_hypoplasia_1|11p_partial_monosomy_syndrome|Congenital_aniridia|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|Autosomal_dominant_keratitis|Irido-corneo-trabecular_dysgenesis": 1,
    "Autosomal_dominant_keratitis|11p_partial_monosomy_syndrome|Anophthalmia-microphthalmia_syndrome|Congenital_aniridia|Foveal_hypoplasia_1|Aniridia|_Cerebellar_Ataxia|_And_Intellectual_Disability|carboxymethyl-dextran-A2-gadolinium-DOTA": 1,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Wilms_tumor_1": 8,
    "Meacham_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4": 12,
    "Meacham_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|not_provided": 2,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Nephroblastoma|11p_partial_monosomy_syndrome": 3,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Nephroblastoma|11p_partial_monosomy_syndrome|not_provided": 1,
    "Meacham_syndrome|Nephroblastoma|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4": 5,
    "Nephrotic_syndrome|_type_4|Nephroblastoma|Meacham_syndrome|11p_partial_monosomy_syndrome|not_provided": 1,
    "Nephrotic_syndrome|_type_4|Nephroblastoma|Meacham_syndrome": 1,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Nephroblastoma": 1,
    "not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome|Wilms_tumor_1": 1,
    "Nephroblastoma|Meacham_syndrome|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4": 6,
    "Wilms_tumor_1|Nephrotic_syndrome|_type_4|Meacham_syndrome": 4,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Wilms_tumor_1|not_provided": 1,
    "Meacham_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1": 1,
    "Nephroblastoma|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome": 3,
    "not_provided|Meacham_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|Drash_syndrome|Frasier_syndrome": 1,
    "Meacham_syndrome|Nephrotic_syndrome|_type_4|not_provided|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1": 1,
    "Wilms_tumor_1|Meacham_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Meacham_syndrome|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|not_provided": 1,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Frasier_syndrome|Drash_syndrome|not_provided|Wilms_tumor_1": 1,
    "Nephrotic_syndrome|_type_4|WT1-related_disorder|Wilms_tumor_1|Meacham_syndrome": 2,
    "Wilms_tumor_1": 722,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 63,
    "Kidney_disorder|Nephrotic_syndrome|_type_4|11p_partial_monosomy_syndrome|Frasier_syndrome|Wilms_tumor_1|Drash_syndrome|Meacham_syndrome|WT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 20,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome": 133,
    "Wilms_tumor_1|Inborn_genetic_diseases|WT1-related_disorder|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases": 20,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|not_provided|Inborn_genetic_diseases|Meacham_syndrome|Mesothelioma|_malignant|Aniridia_1|Nephrotic_syndrome|_type_4": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 64,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 47,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Inborn_genetic_diseases": 41,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome": 130,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 214,
    "Nephrotic_syndrome|_type_4": 21,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome": 24,
    "Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome": 16,
    "Drash_syndrome": 19,
    "Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome": 45,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|not_provided": 3,
    "WT1-related_disorder": 13,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|Meacham_syndrome|Nephrotic_syndrome|_type_4|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant": 17,
    "WT1-related_disorder|11p_partial_monosomy_syndrome|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Meacham_syndrome": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|not_provided|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome": 8,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases": 12,
    "Hereditary_cancer-predisposing_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Drash_syndrome|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome": 13,
    "Frasier_syndrome": 5,
    "not_provided|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 2,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|WT1-related_disorder|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Wilms_tumor_1|Meacham_syndrome|Aniridia_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Hereditary_cancer-predisposing_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Meacham_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome": 22,
    "Wilms_tumor_1|Meacham_syndrome|Nephrotic_syndrome|_type_4|Frasier_syndrome|Drash_syndrome|not_specified|not_provided": 1,
    "Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 10,
    "Familial_idiopathic_steroid-resistant_nephrotic_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|Inborn_genetic_diseases|not_provided|WT1-related_disorder|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "WT1-related_disorder|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Familial_idiopathic_steroid-resistant_nephrotic_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Nephrotic_syndrome|_type_4|not_provided|Nephrotic_range_proteinuria|Leber_congenital_amaurosis_10": 1,
    "Inborn_genetic_diseases|WT1-related_disorder": 1,
    "Disorder_of_sexual_differentiation|Ambiguous_genitalia": 1,
    "WT1-related_disorder|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 22,
    "not_provided|WT1-related_disorder": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 28,
    "WT1-related_disorder|Drash_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Drash_syndrome|Nephrotic_syndrome|_type_4|not_provided": 1,
    "WT1-related_disorder|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "WT1-related_disorder|Drash_syndrome": 1,
    "WT1-related_disorder|Wilms_tumor_1|Drash_syndrome|WT1-related_Wilms_tumor|Kidney_disorder|Frasier_syndrome|11p_partial_monosomy_syndrome|not_provided|Nephrotic_syndrome|_type_4|Aniridia_1|Mesothelioma|_malignant|Meacham_syndrome": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|WT1-related_disorder|Kidney_disorder|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Meacham_syndrome|not_provided|Steroid-resistant_nephrotic_syndrome|Nephrotic_range_proteinuria": 1,
    "Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1": 9,
    "Nephrotic_syndrome|_type_4|Acute_myeloid_leukemia": 1,
    "Frasier_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Drash_syndrome|Wilms_tumor_1|Aniridia_1|11p_partial_monosomy_syndrome|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "Wilms_tumor_1|Meacham_syndrome|Drash_syndrome|Mesothelioma|_malignant|Frasier_syndrome|Nephrotic_syndrome|_type_4|Focal_segmental_glomerulosclerosis|not_provided|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases": 4,
    "Nephrotic_syndrome|_type_4|Frasier_syndrome|Meacham_syndrome|Drash_syndrome": 1,
    "Frasier_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1|Drash_syndrome": 4,
    "Wilms_tumor_1|not_specified|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "WT1-related_disorder|Nephrotic_syndrome|_type_4|Drash_syndrome|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Frasier_syndrome": 1,
    "not_provided|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Inborn_genetic_diseases": 4,
    "Nephrotic_syndrome|_type_4|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases": 3,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided": 2,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Inborn_genetic_diseases": 23,
    "Gonadal_tissue_inappropriate_for_external_genitalia_or_chromosomal_sex|Cholestasis|Gonadal_dysgenesis": 1,
    "Wilms_tumor_1|Meacham_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Mesothelioma|_malignant|Frasier_syndrome|Nephrotic_syndrome|_type_4|Aniridia_1|not_provided": 1,
    "11p_partial_monosomy_syndrome|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Inborn_genetic_diseases|not_specified|Leber_congenital_amaurosis_10": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Aniridia_1|Nephrotic_syndrome|_type_4|not_provided": 1,
    "Nephrotic_range_proteinuria": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Familial_idiopathic_steroid-resistant_nephrotic_syndrome|not_provided": 1,
    "Frasier_syndrome|Nephrotic_syndrome|_type_4|Drash_syndrome|Meacham_syndrome|Wilms_tumor_1|Mesothelioma|_malignant|WT1-related_disorder": 1,
    "not_specified|not_provided|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Nephrotic_syndrome|_type_4": 1,
    "11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|Aniridia_1|Mesothelioma|_malignant|Meacham_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Aniridia_1|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant|not_provided|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 19,
    "Wilms_tumor_1|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Drash_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1|Frasier_syndrome": 2,
    "Inborn_genetic_diseases|Aniridia_1|Mesothelioma|_malignant|Meacham_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4": 1,
    "not_provided|Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 2,
    "WT1-related_disorder|Leber_congenital_amaurosis_10": 1,
    "Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Meacham_syndrome": 2,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|not_provided": 1,
    "Inborn_genetic_diseases|11p_partial_monosomy_syndrome|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome": 3,
    "Inborn_genetic_diseases|Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 5,
    "not_provided|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome": 3,
    "Inborn_genetic_diseases|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "WT1-related_disorder|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "WT1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|Nephrotic_syndrome|_type_4|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Meacham_syndrome": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Focal_segmental_glomerulosclerosis|Inborn_genetic_diseases": 1,
    "not_specified|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided": 1,
    "not_provided|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Aniridia_1|Meacham_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Frasier_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|WT1-related_disorder|Aniridia_1|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant": 2,
    "11p_partial_monosomy_syndrome|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome": 3,
    "not_specified|Inborn_genetic_diseases|Drash_syndrome|Meacham_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|Frasier_syndrome|Mesothelioma|_malignant|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 2,
    "Aniridia_1|Frasier_syndrome|Mesothelioma|_malignant|Drash_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|not_provided|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Inborn_genetic_diseases": 2,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Aniridia_1|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Wilms_tumor_1|Meacham_syndrome|11p_partial_monosomy_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 2,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|not_provided": 1,
    "Wilms_tumor_1|not_provided|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Meacham_syndrome|not_specified": 1,
    "Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome": 1,
    "Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|11p_partial_monosomy_syndrome|not_provided": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|not_provided|WT1-related_Wilms_tumor|Inborn_genetic_diseases|WT1-related_disorder": 1,
    "not_provided|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome": 1,
    "Frasier_syndrome|Wilms_tumor_1|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases": 1,
    "WT1-related_disorder|Inborn_genetic_diseases|not_provided|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 2,
    "Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Wilms_tumor_1|Nephrotic_syndrome|_type_4|11p_partial_monosomy_syndrome": 1,
    "Frasier_syndrome|Wilms_tumor_1|Meacham_syndrome|Drash_syndrome|not_specified|not_provided|Kidney_disorder|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 5,
    "Drash_syndrome|Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|not_provided": 1,
    "Hereditary_cancer|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|WT1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 2,
    "Wilms_tumor_1|Inborn_genetic_diseases": 22,
    "Wilms_tumor_1|Inborn_genetic_diseases|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Wilms_tumor_1": 12,
    "Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome": 1,
    "WT1-related_disorder|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome|Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Wilms_tumor_1|not_provided|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Meacham_syndrome|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Inborn_genetic_diseases|not_provided": 5,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Disorder_of_sexual_differentiation": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|Ovarian_cancer": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided": 4,
    "not_provided|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_specified|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Wilms_tumor_1": 2,
    "Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant": 1,
    "11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1": 4,
    "not_provided|Wilms_tumor_1|Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Mixed_phenotype_acute_leukemia_with_t(v%3B11q23.3)|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases|Aniridia_1|Mesothelioma|_malignant|Meacham_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|Meacham_syndrome|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases": 5,
    "Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Hereditary_cancer-predisposing_syndrome|not_provided|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 2,
    "Wilms_tumor_1|Inborn_genetic_diseases|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome": 3,
    "Wilms_tumor_1|Meacham_syndrome|Frasier_syndrome|Drash_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|11p_partial_monosomy_syndrome": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Meacham_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Aniridia_1": 1,
    "not_provided|Wilms_tumor_1|Meacham_syndrome|not_specified|Nephrotic_syndrome|_type_4|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Mesothelioma|_malignant|Wilms_tumor_1|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Drash_syndrome|Meacham_syndrome|Aniridia_1|Frasier_syndrome": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Meacham_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1|Drash_syndrome": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome": 3,
    "Inborn_genetic_diseases|Meacham_syndrome|Aniridia_1|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant": 1,
    "Hereditary_cancer-predisposing_syndrome|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "11p_partial_monosomy_syndrome|Drash_syndrome|Wilms_tumor_1|Frasier_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Meacham_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|not_specified": 1,
    "not_provided|Wilms_tumor_1": 29,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|WT1-related_disorder": 1,
    "WT1-related_disorder|Wilms_tumor_1": 1,
    "Inborn_genetic_diseases|WT1-related_disorder|Nephrotic_syndrome|_type_4|Meacham_syndrome|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Drash_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Meacham_syndrome|Drash_syndrome|not_specified|Nephrotic_syndrome|_type_4|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "WT1-related_disorder|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "not_specified|Wilms_tumor_1|Mesothelioma|_malignant|Meacham_syndrome|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|11p_partial_monosomy_syndrome": 1,
    "Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Drash_syndrome|Nephrotic_syndrome|_type_4|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|WT1-related_disorder|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Aniridia_1|Proteinuria|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Inborn_genetic_diseases|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 2,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|WT1-related_disorder|Microscopic_hematuria|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "not_provided|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|Aniridia_1|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome": 6,
    "Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Wilms_tumor_1|not_provided|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Inborn_genetic_diseases|Wilms_tumor_1|not_provided|Mesothelioma|_malignant|Frasier_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome": 6,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Aniridia_1|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "not_provided|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|WT1-related_disorder|Inborn_genetic_diseases|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 2,
    "Wilms_tumor_1|Meacham_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Aniridia_1|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|not_provided|WT1-related_disorder|Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Aniridia_1|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|not_provided|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Inborn_genetic_diseases|not_provided|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome": 1,
    "WT1-related_disorder|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Nephrotic_syndrome|_type_4|not_specified|not_provided": 1,
    "Mesothelioma|_malignant|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Aniridia_1|Meacham_syndrome|Frasier_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|not_specified": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Meacham_syndrome|Mesothelioma|_malignant|Aniridia_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|Mesothelioma|_malignant|Aniridia_1|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Inborn_genetic_diseases|Meacham_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Drash_syndrome|Nephrotic_syndrome|_type_4|Aniridia_1|not_provided": 1,
    "Mesothelioma|_malignant|Meacham_syndrome|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Nephrotic_syndrome|_type_4|Aniridia_1|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome": 2,
    "not_provided|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome": 1,
    "Frasier_syndrome|Mesothelioma|_malignant|Wilms_tumor_1|Drash_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|WT1-related_disorder|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 3,
    "Frasier_syndrome|Wilms_tumor_1|Meacham_syndrome|Nephrotic_syndrome|_type_4|not_provided|Inborn_genetic_diseases|Drash_syndrome|11p_partial_monosomy_syndrome|not_specified|WT1-related_disorder": 1,
    "not_provided|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 4,
    "Inborn_genetic_diseases|Aniridia_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|not_provided": 21,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|Meacham_syndrome|not_provided|Nephrotic_syndrome|_type_4": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Wilms_tumor_1|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Drash_syndrome|Inborn_genetic_diseases|Frasier_syndrome|11p_partial_monosomy_syndrome|not_provided": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Meacham_syndrome|Inborn_genetic_diseases": 1,
    "WT1-related_disorder|Wilms_tumor_1|Aniridia_1|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Meacham_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Meacham_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Wilms_tumor_1|Meacham_syndrome|Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Meacham_syndrome|not_provided|Kidney_disorder|Nephrotic_syndrome|_type_4|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_specified": 1,
    "Nephrotic_syndrome|_type_4|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|not_provided": 6,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|not_provided": 1,
    "Meacham_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Frasier_syndrome|Wilms_tumor_1|not_provided": 1,
    "not_specified|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome": 1,
    "Frasier_syndrome|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Drash_syndrome|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Aniridia_1|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Meacham_syndrome|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|WT1-related_disorder": 1,
    "Leber_congenital_amaurosis_10": 9,
    "Hereditary_cancer-predisposing_syndrome|Aniridia_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Nephroblastoma|not_provided|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|WT1-related_disorder|11p_partial_monosomy_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Meacham_syndrome": 1,
    "Corticosteroids_response|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Drash_syndrome|Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Meacham_syndrome|Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|not_specified": 1,
    "Wilms_tumor_1|Drash_syndrome|not_provided|Frasier_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|not_provided|Meacham_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Mesothelioma|_malignant|Aniridia_1|Frasier_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Aniridia_1|Meacham_syndrome": 1,
    "Wilms_tumor_1|Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|not_provided": 2,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|not_provided": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome|Meacham_syndrome": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|WT1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Drash_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome": 1,
    "Drash_syndrome|Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Inborn_genetic_diseases|Drash_syndrome": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Hereditary_cancer-predisposing_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Meacham_syndrome": 1,
    "not_specified|Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|not_provided|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4": 1,
    "not_provided|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|WT1-related_disorder|11p_partial_monosomy_syndrome": 1,
    "Nephrotic_syndrome|_type_4|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Frasier_syndrome|11p_partial_monosomy_syndrome|Drash_syndrome|Wilms_tumor_1": 5,
    "Wilms_tumor_1|Drash_syndrome|Inborn_genetic_diseases|11p_partial_monosomy_syndrome|Frasier_syndrome": 1,
    "11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "WT1-related_disorder|Disorder_of_sexual_differentiation|Inborn_genetic_diseases|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Meacham_syndrome": 1,
    "Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome": 2,
    "Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1": 1,
    "Nephroblastoma|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|11p_partial_monosomy_syndrome|Meacham_syndrome": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|WT1-related_disorder|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 1,
    "Nephroblastoma|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Meacham_syndrome|11p_partial_monosomy_syndrome": 1,
    "Drash_syndrome|Inborn_genetic_diseases|Aniridia_1|Wilms_tumor_1|11p_partial_monosomy_syndrome|Mesothelioma|_malignant|Meacham_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Aniridia_1|Frasier_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|not_provided": 1,
    "not_specified|WT1-related_disorder|Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|Meacham_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|Meacham_syndrome|not_specified|Nephrotic_syndrome|_type_4|Drash_syndrome|Frasier_syndrome|not_provided|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 2,
    "Drash_syndrome|Hereditary_cancer-predisposing_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Drash_syndrome|not_specified|Frasier_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Drash_syndrome|not_provided|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|not_specified|not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|WT1-related_disorder": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|Drash_syndrome": 2,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis|not_provided|Meacham_syndrome|not_specified": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|not_provided|Nephrotic_syndrome|_type_4|Hereditary_cancer-predisposing_syndrome|WT1-related_disorder|Inborn_genetic_diseases": 1,
    "Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Inborn_genetic_diseases|11p_partial_monosomy_syndrome": 1,
    "Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Aniridia_1|Nephrotic_syndrome|_type_4|not_provided": 1,
    "Wilms_tumor_1|Drash_syndrome|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Meacham_syndrome|Mesothelioma|_malignant|Drash_syndrome|Frasier_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|WT1-related_disorder|Inborn_genetic_diseases|Precursor_B-cell_acute_lymphoblastic_leukemia|not_provided|11p_partial_monosomy_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Wilms_tumor_1|Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant|11p_partial_monosomy_syndrome": 1,
    "Nephroblastoma|Nephrotic_syndrome|_type_4|Meacham_syndrome|11p_partial_monosomy_syndrome": 2,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Wilms_tumor_1|not_provided|Frasier_syndrome|Drash_syndrome|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Nephrotic_syndrome|_type_4|Meacham_syndrome|Drash_syndrome|not_provided|Inborn_genetic_diseases|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome": 1,
    "Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Wilms_tumor_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Aniridia_1|Frasier_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Drash_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "11p_partial_monosomy_syndrome|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|not_provided": 1,
    "WT1-related_disorder|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|not_provided|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Drash_syndrome|WT1-related_disorder": 1,
    "Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Inborn_genetic_diseases|Nephrotic_syndrome|_type_4|not_provided|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Frasier_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Wilms_tumor_1|Meacham_syndrome|Mesothelioma|_malignant|Inborn_genetic_diseases|not_provided|11p_partial_monosomy_syndrome": 1,
    "not_provided|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Frasier_syndrome|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Nephrotic_syndrome|_type_4|Mesothelioma|_malignant|Meacham_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Wilms_tumor_1": 1,
    "Inborn_genetic_diseases|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided": 1,
    "WT1-related_disorder|Frasier_syndrome|Drash_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Drash_syndrome|Frasier_syndrome|Wilms_tumor_1|11p_partial_monosomy_syndrome|not_provided|Aniridia_1|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Hereditary_cancer-predisposing_syndrome|WT1-related_disorder": 1,
    "Aniridia_1|Frasier_syndrome|Drash_syndrome|Meacham_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4|Wilms_tumor_1|11p_partial_monosomy_syndrome|Hereditary_cancer-predisposing_syndrome|WT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Wilms_tumor_1|WT1-related_disorder|Drash_syndrome|Frasier_syndrome|11p_partial_monosomy_syndrome": 1,
    "Wilms_tumor_1|11p_partial_monosomy_syndrome|Drash_syndrome|Frasier_syndrome|not_provided|Nephrotic_syndrome|_type_4|Meacham_syndrome|Mesothelioma|_malignant": 1,
    "Nephroblastoma|Nephrotic_syndrome|_type_4|11p_partial_monosomy_syndrome|Meacham_syndrome": 3,
    "Nephroblastoma|Nephrotic_syndrome|_type_4|not_provided|11p_partial_monosomy_syndrome|Meacham_syndrome": 1,
    "Meacham_syndrome|Nephrotic_syndrome|_type_4|WT1-related_disorder|Drash_syndrome|Wilms_tumor_1": 1,
    "Meacham_syndrome|Wilms_tumor_1|Nephrotic_syndrome|_type_4|WT1-related_disorder|not_provided": 1,
    "Meacham_syndrome|Wilms_tumor_1|Drash_syndrome|Frasier_syndrome|Mesothelioma|_malignant|Nephrotic_syndrome|_type_4": 1,
    "PRRG4-related_disorder": 6,
    "Primary_CD59_deficiency": 10,
    "not_provided|Primary_CD59_deficiency": 1,
    "CD59-related_disorder": 1,
    "Inborn_genetic_diseases|CD59-related_disorder": 1,
    "not_provided|CD59-related_disorder": 1,
    "CD59-related_disorder|not_provided": 1,
    "Primary_CD59_deficiency|not_provided": 1,
    "Autism|Intellectual_disability|_moderate|Autistic_behavior|Seizure": 1,
    "CAPRIN1-related_disorder": 3,
    "Neurodevelopmental_disorder_with_language_impairment|_autism|_and_attention_deficit-hyperactivity_disorder": 7,
    "CAPRIN1-related_neurodevelopmental_disorders": 1,
    "not_provided|Cerebellar_ataxia|Neurodegeneration|_childhood-onset|_with_cerebellar_ataxia_and_cognitive_decline": 1,
    "Neurodegeneration|_childhood-onset|_with_cerebellar_ataxia_and_cognitive_decline": 1,
    "Focal-onset_seizure|Moderate_global_developmental_delay|Epileptic_encephalopathy": 1,
    "CAPRIN1-associated_disorder": 1,
    "Acatalasia": 2,
    "Acatalasemia|_japanese_type": 2,
    "not_provided|CAT-related_disorder": 3,
    "Acatalasia|CAT-related_disorder|not_provided": 1,
    "Acatalasia|Intellectual_disability": 1,
    "CAT-related_disorder|not_provided": 1,
    "CAT-related_disorder": 1,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 53,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided": 21,
    "not_provided|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 20,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency": 371,
    "Pyruvate_dehydrogenase_complex_deficiency|not_provided": 3,
    "not_specified|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 2,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_specified|not_provided": 5,
    "not_specified|Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided": 4,
    "not_provided|PDHX-related_disorder|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 1,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided|not_specified": 2,
    "not_provided|Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_specified": 5,
    "PDHX-related_disorder|Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided": 2,
    "not_provided|Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_specified|PDHX-related_disorder": 2,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided|PDHX-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 2,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided|not_specified|PDHX-related_disorder": 1,
    "Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E3-binding_protein_deficiency|not_provided": 3,
    "not_specified|not_provided|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 2,
    "not_provided|not_specified|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 2,
    "PDHX-related_disorder|not_specified|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency|Pyruvate_dehydrogenase_E3-binding_protein_deficiency": 1,
    "not_provided|PDHX-related_disorder": 1,
    "PDHX-related_disorder|not_provided": 1,
    "not_provided|Pyruvate_dehydrogenase_E3-binding_protein_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|PDHX-related_disorder|not_provided": 1,
    "INDIAN_BLOOD_GROUP_SYSTEM_POLYMORPHISM": 1,
    "not_specified|CD44-related_disorder": 1,
    "not_provided|CD44-related_disorder": 1,
    "CD44-related_disorder": 7,
    "CD44-related_disorder|not_provided": 1,
    "Blood_group|_Indian_system": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_41": 10,
    "SLC1A2-related_disorder|not_provided": 7,
    "Developmental_and_epileptic_encephalopathy|_41|not_provided": 11,
    "Developmental_and_epileptic_encephalopathy|_41": 25,
    "SLC1A2-related_disorder": 3,
    "not_provided|SLC1A2-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy|_41|SLC1A2-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_41|not_provided|Inborn_genetic_diseases": 1,
    "SLC1A2-related_disorder|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_41|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_41|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SLC1A2-related_disorder|Developmental_and_epileptic_encephalopathy|_41|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SLC1A2-related_disorder|not_specified": 1,
    "TRIM44-related_disorder": 2,
    "Aniridia_3": 2,
    "not_provided|Aniridia_3": 2,
    "not_specified|TRAF6-related_disorder": 1,
    "TRAF6-related_disorder": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 43,
    "Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 4,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency_disease|not_provided|Recombinase_activating_gene_1_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 470,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_1_deficiency": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_1_deficiency|Inborn_genetic_diseases": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis": 1,
    "Inborn_genetic_diseases|Recombinase_activating_gene_1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Inborn_genetic_diseases": 3,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 363,
    "Inborn_genetic_diseases|Recombinase_activating_gene_1_deficiency": 1,
    "Recombinase_activating_gene_1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 2,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_1_deficiency": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 20,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 15,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 33,
    "RAG1-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Inborn_genetic_diseases": 7,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis": 3,
    "not_provided|Recombinase_activating_gene_1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified": 2,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided|RAG1-related_disorder|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_1_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "not_specified|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 3,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis": 13,
    "Inborn_genetic_diseases|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 9,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided": 4,
    "Recombinase_activating_gene_1_deficiency|not_specified|not_provided|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 2,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 14,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|RAG1-related_disorder|Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided": 1,
    "Inherited_Immunodeficiency_Diseases|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Microcephaly": 1,
    "not_provided|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Pelizaeus-Merzbacher_disease|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "not_provided|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 4,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas": 2,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Recombinase_activating_gene_1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis": 2,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_B_cell-negative|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis": 1,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 3,
    "Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Recombinase_activating_gene_1_deficiency|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 2,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 3,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis|not_specified|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|RAG1-related_disorder": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 10,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_disease": 1,
    "not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 19,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Recombinase_activating_gene_1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified": 2,
    "not_specified|Combined_immunodeficiency_with_skin_granulomas|Immunodeficiency_104|Recombinase_activating_gene_1_deficiency|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Recombinase_activating_gene_1_deficiency": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 7,
    "not_provided|Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis|not_specified|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Tumor_predisposition_syndrome_3|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Inborn_genetic_diseases": 1,
    "Recombinase_activating_gene_1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_specified": 4,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Recombinase_activating_gene_1_deficiency|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified": 1,
    "not_specified|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis": 2,
    "not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis": 1,
    "RAG1-related_disorder|not_provided|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_disease": 1,
    "not_provided|Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "RAG1-related_disorder|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Recombinase_activating_gene_1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|not_provided|Recombinase_activating_gene_1_deficiency|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "not_provided|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease": 1,
    "not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided": 1,
    "Recombinase_activating_gene_1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|RAG1-related_disorder": 1,
    "Cataract_3_multiple_types|not_provided": 2,
    "RAG1-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_B_cell-negative|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided": 2,
    "RAG1-related_disorder": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "not_provided|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_1_deficiency|not_provided": 2,
    "Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "Inherited_Immunodeficiency_Diseases|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided": 1,
    "not_specified|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_specified|not_provided|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "not_provided|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_1_deficiency": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency|_B_cell-negative|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease|RAG1-related_disorder": 1,
    "Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 2,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Inborn_genetic_diseases": 1,
    "RAG1-related_disorder|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 1,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_1_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Immunodeficiency_104|not_specified|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 2,
    "not_provided|RAG1-related_disorder": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 3,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_specified|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_1_deficiency": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Primary_ciliary_dyskinesia|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency_disease|not_provided|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_provided|Recombinase_activating_gene_1_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Recombinase_activating_gene_1_deficiency|not_specified|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|not_specified|not_provided": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|not_specified": 1,
    "Severe_combined_immunodeficiency|_B_cell-negative|Recombinase_activating_gene_1_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|RAG1-related_disorder|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "not_provided|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency_disease|not_provided|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|RAG1-related_disorder|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Combined_immunodeficiency_due_to_partial_RAG1_deficiency|Histiocytic_medullary_reticulosis|not_specified|not_provided": 1,
    "RAG1-related_disorder|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided|Histiocytic_medullary_reticulosis|not_specified|RAG1-related_disorder": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_due_to_partial_RAG1_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|Histiocytic_medullary_reticulosis": 8,
    "not_provided|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 3,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 1,
    "RAG2-related_disorder|Histiocytic_medullary_reticulosis|not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|not_provided|Inborn_genetic_diseases|Histiocytic_medullary_reticulosis": 1,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|not_provided|RAG2-related_disorder": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|RAG2-related_disorder": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|not_specified": 1,
    "Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity": 2,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Inborn_genetic_diseases|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Recombinase_activating_gene_2_deficiency|not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|not_provided": 1,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis": 1,
    "Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Atypical_severe_combined_immunodeficiency_due_to_complete_RAG1/2_deficiency|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 18,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity": 6,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Recombinase_activating_gene_2_deficiency|Combined_immunodeficiency_with_skin_granulomas|Inborn_error_of_immunity|Common_variable_immunodeficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Inborn_error_of_immunity": 1,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Atypical_severe_combined_immunodeficiency_due_to_complete_RAG1/2_deficiency|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|not_specified": 1,
    "Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Histiocytic_medullary_reticulosis|RAG2-related_disorder|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|RAG2-related_disorder|Histiocytic_medullary_reticulosis": 2,
    "Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|not_specified|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency|not_provided|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_with_skin_granulomas|not_provided|Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 2,
    "Histiocytic_medullary_reticulosis|Inborn_genetic_diseases|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "not_provided|Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency": 3,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency": 1,
    "Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Inborn_genetic_diseases|Histiocytic_medullary_reticulosis": 1,
    "not_provided|Histiocytic_medullary_reticulosis|not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|not_provided|Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|not_provided": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|not_specified|not_provided|Severe_combined_immunodeficiency|_B_cell-negative": 1,
    "Atypical_severe_combined_immunodeficiency_due_to_complete_RAG1/2_deficiency|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|not_provided": 1,
    "not_specified|Recombinase_activating_gene_2_deficiency|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified|RAG2-related_disorder|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Combined_immunodeficiency_with_skin_granulomas|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "not_provided|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "not_provided|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "not_specified|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|RAG2-related_disorder": 1,
    "Recombinase_activating_gene_2_deficiency|Inborn_genetic_diseases|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity": 2,
    "Histiocytic_medullary_reticulosis|Atypical_severe_combined_immunodeficiency_due_to_complete_RAG1/2_deficiency|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Immunodeficiency_104": 1,
    "Severe_combined_immunodeficiency_disease|Recombinase_activating_gene_2_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Inborn_genetic_diseases": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Inborn_genetic_diseases|Histiocytic_medullary_reticulosis": 1,
    "not_provided|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Recombinase_activating_gene_2_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Combined_immunodeficiency_with_skin_granulomas": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Inborn_error_of_immunity|Severe_combined_immunodeficiency|_B_cell-negative|Histiocytic_medullary_reticulosis": 1,
    "Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|RAG2-related_disorder|Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|Severe_combined_immunodeficiency_disease": 1,
    "Atypical_severe_combined_immunodeficiency_due_to_complete_RAG1/2_deficiency|Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|RAG2-related_disorder|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Recombinase_activating_gene_2_deficiency": 1,
    "Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency": 2,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|Recombinase_activating_gene_2_deficiency": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas": 4,
    "Inborn_genetic_diseases|Recombinase_activating_gene_2_deficiency": 1,
    "Recombinase_activating_gene_2_deficiency|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|not_specified": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Combined_immunodeficiency_with_skin_granulomas|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Recombinase_activating_gene_2_deficiency|Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_with_skin_granulomas|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Histiocytic_medullary_reticulosis|not_provided": 1,
    "Salla_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Recombinase_activating_gene_2_deficiency|Inborn_error_of_immunity|not_provided": 1,
    "LRRC4C-related_disorder": 2,
    "not_provided|Exostoses|_multiple|_type_2": 22,
    "Exostoses|_multiple|_type_2|not_provided": 23,
    "Exostoses|_multiple|_type_2": 617,
    "not_provided|Exostoses|_multiple|_type_2|not_specified": 1,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome": 23,
    "EXT2-related_disorder|Multiple_congenital_exostosis": 1,
    "Exostoses|_multiple|_type_2|EXT2-related_disorder": 10,
    "Seizures-scoliosis-macrocephaly_syndrome|not_provided|Exostoses|_multiple|_type_2": 1,
    "Exostoses|_multiple|_type_1|not_provided|not_specified|Exostoses|_multiple|_type_2": 1,
    "Inborn_genetic_diseases|Exostoses|_multiple|_type_2": 16,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|not_provided|EXT2-related_disorder": 2,
    "Exostoses|_multiple|_type_2|Inborn_genetic_diseases": 19,
    "EXT2-related_disorder|Exostoses|_multiple|_type_2": 8,
    "not_specified|Exostoses|_multiple|_type_2|not_provided|Exostoses|_multiple|_type_1": 1,
    "EXT2-related_disorder": 12,
    "Seizures-scoliosis-macrocephaly_syndrome|Exostoses|_multiple|_type_2|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Exostoses|_multiple|_type_2|not_provided": 1,
    "not_provided|not_specified|Exostoses|_multiple|_type_2": 1,
    "not_specified|Exostoses|_multiple|_type_2|Exostoses|_multiple|_type_1|not_provided": 2,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|not_provided": 4,
    "Seizures-scoliosis-macrocephaly_syndrome|Exostoses|_multiple|_type_2": 9,
    "Seizures-scoliosis-macrocephaly_syndrome|Multiple_congenital_exostosis|Exostoses|_multiple|_type_2|EXT2-related_disorder": 1,
    "Exostoses|_multiple|_type_2|Ovarian_cancer": 2,
    "not_provided|Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Exostoses|_multiple|_type_2": 3,
    "Exostoses|_multiple|_type_1|Seizures-scoliosis-macrocephaly_syndrome|Exostoses|_multiple|_type_2|not_provided": 1,
    "Exostoses|_multiple|_type_2|not_specified|not_provided|EXT2-related_disorder": 1,
    "Seizures-scoliosis-macrocephaly_syndrome|Exostoses|_multiple|_type_2|not_provided": 2,
    "Multiple_congenital_exostosis|not_provided|Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome": 1,
    "Exostoses|_multiple|_type_2|not_provided|Inborn_genetic_diseases": 2,
    "EXT2-related_disorder|Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|not_provided": 1,
    "Seizures-scoliosis-macrocephaly_syndrome|Exostoses|_multiple|_type_2|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Exostoses|_multiple|_type_2": 1,
    "Exostoses|_multiple|_type_2|not_specified|not_provided": 1,
    "EXT2-related_disorder|Inborn_genetic_diseases|Exostoses|_multiple|_type_2": 2,
    "Exostoses|_multiple|_type_2|Inborn_genetic_diseases|Seizures-scoliosis-macrocephaly_syndrome": 1,
    "Exostoses|_multiple|_type_2|Inborn_genetic_diseases|Ovarian_cancer": 1,
    "Exostoses|_multiple|_type_2|EXT2-related_disorder|not_provided": 1,
    "not_provided|EXT2-related_disorder|Exostoses|_multiple|_type_2": 1,
    "Seizures-scoliosis-macrocephaly_syndrome": 2,
    "Exostoses|_multiple|_type_2|not_provided|not_specified": 1,
    "not_provided|Exostoses|_multiple|_type_2|Exostoses|_multiple|_type_1": 1,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|Exostoses|_multiple|_type_1|not_provided": 1,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|not_provided|not_specified": 1,
    "EXT2-related_disorder|not_specified|Exostoses|_multiple|_type_2": 1,
    "Exostoses|_multiple|_type_2|Multiple_congenital_exostosis": 1,
    "not_provided|Exostoses|_multiple|_type_1|Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|not_specified": 1,
    "Exostoses|_multiple|_type_2|not_provided|EXT2-related_disorder|Exostoses|_multiple|_type_1": 1,
    "not_specified|Exostoses|_multiple|_type_2|not_provided": 3,
    "Ovarian_cancer|Exostoses|_multiple|_type_2": 1,
    "not_provided|Exostoses|_multiple|_type_1|Exostoses|_multiple|_type_2|not_specified": 1,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|EXT2-related_disorder|Inborn_genetic_diseases": 1,
    "EXT2-related_disorder|Seizures-scoliosis-macrocephaly_syndrome|not_specified|not_provided|Exostoses|_multiple|_type_2": 1,
    "Exostoses|_multiple|_type_2|EXT2-related_disorder|Exostoses|_multiple|_type_1": 1,
    "Exostoses|_multiple|_type_2|not_provided|Seizures-scoliosis-macrocephaly_syndrome": 2,
    "Inborn_genetic_diseases|Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome": 1,
    "not_provided|EXT2-related_disorder|Inborn_genetic_diseases|Exostoses|_multiple|_type_2": 1,
    "not_provided|Inborn_genetic_diseases|Exostoses|_multiple|_type_2|not_specified": 1,
    "Exostoses|_multiple|_type_2|not_provided|EXT2-related_disorder": 1,
    "EXT2-related_disorder|not_specified|not_provided|Exostoses|_multiple|_type_2": 1,
    "Exostoses|_multiple|_type_2|Exostoses|_multiple|_type_1|not_provided": 1,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|not_specified": 1,
    "Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome|EXT2-related_disorder": 1,
    "not_specified|Exostoses|_multiple|_type_1|not_provided|Exostoses|_multiple|_type_2": 1,
    "Inborn_genetic_diseases|not_provided|Exostoses|_multiple|_type_2|Seizures-scoliosis-macrocephaly_syndrome": 1,
    "Hereditary_Multiple_Osteochondromatosis|Exostoses|_multiple|_type_2": 1,
    "Exostoses|_multiple|_type_2|not_specified": 1,
    "Parietal_foramina_2": 125,
    "not_provided|Parietal_foramina_2": 16,
    "Parietal_foramina_2|not_provided": 13,
    "Frontonasal_dysplasia_with_alopecia_and_genital_anomaly": 5,
    "Inborn_genetic_diseases|Parietal_foramina_2": 3,
    "not_provided|ALX4-related_disorder": 2,
    "ALX4-related_disorder|Parietal_foramina_2|not_provided": 1,
    "ALX4-related_disorder|not_provided": 1,
    "not_provided|Frontonasal_dysplasia_with_alopecia_and_genital_anomaly|Parietal_foramina_2": 5,
    "not_provided|Frontonasal_dysplasia_with_alopecia_and_genital_anomaly": 2,
    "ALX4-related_disorder": 5,
    "not_specified|Parietal_foramina_2|not_provided": 1,
    "Frontonasal_dysplasia_with_alopecia_and_genital_anomaly|Inborn_genetic_diseases|not_provided": 1,
    "Frontonasal_dysplasia_with_alopecia_and_genital_anomaly|Parietal_foramina_2|not_provided": 1,
    "Parietal_foramina_2|Inborn_genetic_diseases": 2,
    "Craniosynostosis_5|_susceptibility_to": 2,
    "not_specified|not_provided|Frontonasal_dysplasia_with_alopecia_and_genital_anomaly|Parietal_foramina_2": 2,
    "Parietal_foramina_2|Inborn_genetic_diseases|not_provided": 1,
    "Parietal_foramina_2|ALX4-related_disorder|not_provided": 1,
    "not_provided|Frontonasal_dysplasia_with_alopecia_and_genital_anomaly|Craniosynostosis_5|_susceptibility_to|Parietal_foramina_2": 1,
    "not_provided|Parietal_foramina_2|Craniosynostosis_5|_susceptibility_to|Frontonasal_dysplasia_with_alopecia_and_genital_anomaly|ALX4-related_disorder": 1,
    "Optic_nerve_glioma": 2,
    "TSPAN18-related_disorder": 6,
    "Leukocyte_adhesion_deficiency_type_II": 229,
    "not_provided|Leukocyte_adhesion_deficiency_type_II": 15,
    "Leukocyte_adhesion_deficiency_type_II|not_provided": 7,
    "Leukocyte_adhesion_deficiency_type_II|not_specified|not_provided": 1,
    "Leukocyte_adhesion_deficiency_type_II|Inborn_genetic_diseases": 16,
    "Inborn_genetic_diseases|not_provided|Leukocyte_adhesion_deficiency_type_II": 2,
    "Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_type_II": 10,
    "SLC35C1-related_disorder|Leukocyte_adhesion_deficiency_type_II": 2,
    "SLC35C1-related_disorder|not_provided|Leukocyte_adhesion_deficiency_type_II": 2,
    "not_specified|not_provided|Leukocyte_adhesion_deficiency_type_II": 3,
    "Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_type_II|not_provided": 1,
    "Leukocyte_adhesion_deficiency_type_II|SLC35C1-related_disorder": 1,
    "SLC35C1-related_disorder": 2,
    "SLC35C1-related_disorder|not_specified|not_provided|Leukocyte_adhesion_deficiency_type_II": 1,
    "Leukocyte_adhesion_deficiency_type_II|not_specified": 1,
    "not_provided|not_specified|Leukocyte_adhesion_deficiency_type_II": 1,
    "SLC35C1-related_disorder|Intellectual_disability|not_specified|Leukocyte_adhesion_deficiency_type_II|not_provided": 1,
    "MAPK8IP1-related_disorder": 5,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)": 15,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|not_provided": 1,
    "not_provided|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 3,
    "PEX16-related_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 2,
    "PEX16-related_disorder": 11,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|PEX16-related_disorder": 2,
    "Peroxisome_biogenesis_disorder_8B": 9,
    "not_provided|PEX16-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder_8A_(Zellweger)|not_provided": 1,
    "not_specified|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder|PEX16-related_disorder": 12,
    "not_provided|PEX16-related_disorder|Peroxisome_biogenesis_disorder": 2,
    "PEX16-related_disorder|Peroxisome_biogenesis_disorder": 9,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|PEX16-related_disorder": 1,
    "PEX16-related_disorder|not_provided|Peroxisome_biogenesis_disorder": 2,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder_8B|not_provided|PEX16-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder|PEX16-related_disorder|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder|not_provided|not_specified": 1,
    "Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder_8B": 1,
    "Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|PEX16-related_disorder": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)|not_provided": 1,
    "not_provided|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_due_to_PEX16_defect": 1,
    "Methylmalonic_aciduria_due_to_methylmalonyl-CoA_mutase_deficiency|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 5,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder_8B|not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder": 3,
    "Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 1,
    "PEX16-related_disorder|Peroxisome_biogenesis_disorder|Microcephaly": 1,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder|PEX16-related_disorder": 1,
    "PEX16-related_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|Inborn_genetic_diseases": 1,
    "not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder|PEX16-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder|not_provided|PEX16-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder|Inborn_genetic_diseases|PEX16-related_disorder": 1,
    "Peroxisome_biogenesis_disorder|PEX16-related_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder_8B|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_specified|Peroxisome_biogenesis_disorder": 1,
    "not_specified|Peroxisome_biogenesis_disorder_8A_(Zellweger)|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_8A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder|PEX16-related_disorder|Peroxisome_biogenesis_disorder_8B|Peroxisome_biogenesis_disorder_8A_(Zellweger)|not_provided": 1,
    "not_provided|PEX16-related_disorder|Peroxisome_biogenesis_disorder|not_specified|Peroxisome_biogenesis_disorder_8A_(Zellweger)": 1,
    "not_provided|PHF21A-related_disorder": 7,
    "PHF21A-related_disorder|not_provided": 4,
    "Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures|not_provided": 6,
    "not_provided|Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures": 1,
    "not_provided|Inborn_genetic_diseases|PHF21A-related_disorder": 1,
    "Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures": 28,
    "Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|PHF21A-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability|Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures": 1,
    "PHF21A-related_disorder": 4,
    "PHF21A-related_disorder|Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures": 1,
    "not_provided|Intellectual_developmental_disorder_with_behavioral_abnormalities_and_craniofacial_dysmorphism_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta_type_16": 11,
    "not_provided|Osteogenesis_imperfecta_type_16": 2,
    "not_provided|Osteogenesis_imperfecta_type_16|not_specified": 1,
    "CREB3L1-related_disorder": 3,
    "Osteogenesis_imperfecta_type_16|not_provided": 4,
    "Osteogenesis_imperfecta_type_16|not_specified|not_provided": 2,
    "CREB3L1-related_disorder|not_provided|not_specified": 1,
    "CREB3L1-related_disorder|not_provided|Osteogenesis_imperfecta_type_16": 1,
    "not_provided|CREB3L1-related_disorder": 4,
    "Osteogenesis_imperfecta_type_16|Inborn_genetic_diseases": 1,
    "not_provided|Osteogenesis_imperfecta_type_16|Inborn_genetic_diseases": 1,
    "CREB3L1-related_disorder|not_provided": 3,
    "Osteogenesis_imperfecta_type_16|Osteogenesis_imperfecta": 1,
    "CREB3L1-related_disorder|Osteogenesis_imperfecta_type_16|not_provided": 1,
    "CREB3L1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "atypical_cerebral_palsy|not_provided": 1,
    "AMBRA1-related_disorder": 7,
    "Exudative_vitreoretinopathy_1": 106,
    "not_provided|ZNF408-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|ZNF408-related_disorder": 1,
    "Retinitis_pigmentosa_72": 2,
    "Retinal_dystrophy|Exudative_vitreoretinopathy_6|not_provided": 1,
    "Exudative_vitreoretinopathy_1|not_provided": 5,
    "not_provided|Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72|Retinal_dystrophy": 1,
    "ZNF408-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72": 1,
    "Exudative_vitreoretinopathy_6|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_6": 1,
    "ZNF408-related_disorder|not_provided": 3,
    "Exudative_vitreoretinopathy_6|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72|not_provided": 1,
    "Inborn_genetic_diseases|Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Retinal_dystrophy": 1,
    "Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72": 1,
    "not_provided|Exudative_vitreoretinopathy_6|Retinitis_pigmentosa_72|Inborn_genetic_diseases": 1,
    "Congenital_prothrombin_deficiency": 247,
    "Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect": 12,
    "Ischemic_stroke|Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect|Pregnancy_loss|_recurrent|_susceptibility_to|_2": 2,
    "Congenital_prothrombin_deficiency|not_provided|Thrombophilia_due_to_thrombin_defect|not_specified": 1,
    "not_provided|Congenital_prothrombin_deficiency": 3,
    "Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|not_provided|Congenital_prothrombin_deficiency": 2,
    "Congenital_prothrombin_deficiency|Coagulation_factor_deficiency_syndrome": 1,
    "Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|Congenital_prothrombin_deficiency": 2,
    "Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_2|Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect": 1,
    "Ischemic_stroke|Congenital_prothrombin_deficiency|Pregnancy_loss|_recurrent|_susceptibility_to|_2|Thrombophilia_due_to_thrombin_defect": 3,
    "Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect": 2,
    "Thrombophilia_due_to_thrombin_defect|not_specified|Congenital_prothrombin_deficiency|not_provided": 1,
    "F2-related_disorder": 3,
    "Thrombophilia_due_to_thrombin_defect|not_specified|not_provided|Congenital_prothrombin_deficiency": 3,
    "Thrombophilia_due_to_thrombin_defect|not_specified|Congenital_prothrombin_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_prothrombin_deficiency|Inborn_genetic_diseases": 6,
    "Congenital_prothrombin_deficiency|not_provided": 4,
    "Thrombophilia_due_to_thrombin_defect|Congenital_prothrombin_deficiency|Pregnancy_loss|_recurrent|_susceptibility_to|_2|Ischemic_stroke|not_specified|not_provided|PROTHROMBIN_TYPE_3|Cerebral_palsy": 1,
    "Inborn_genetic_diseases|Congenital_prothrombin_deficiency": 9,
    "F2-related_disorder|Congenital_prothrombin_deficiency": 2,
    "Congenital_prothrombin_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_prothrombin_deficiency": 8,
    "Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases|Congenital_prothrombin_deficiency|not_provided": 1,
    "Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect|F2-related_disorder": 1,
    "Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect|Inborn_genetic_diseases": 2,
    "Congenital_prothrombin_deficiency|F2-related_disorder|Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect": 1,
    "Prolonged_prothrombin_time|not_provided": 1,
    "Prolonged_prothrombin_time": 2,
    "DYSPROTHROMBINEMIA_PROTHROMBIN_HIMI-II": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_prothrombin_deficiency|F2-related_disorder|Inborn_genetic_diseases": 1,
    "Ischemic_stroke|Congenital_prothrombin_deficiency|Pregnancy_loss|_recurrent|_susceptibility_to|_2|Thrombophilia_due_to_thrombin_defect|F2-related_disorder": 1,
    "F2-related_disorder|Inborn_genetic_diseases|Congenital_prothrombin_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|not_provided|Congenital_prothrombin_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|not_specified|Congenital_prothrombin_deficiency": 1,
    "not_provided|Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect": 2,
    "Congenital_prothrombin_deficiency|not_specified": 1,
    "Thrombophilia_due_to_thrombin_defect|Congenital_prothrombin_deficiency|Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_2|not_provided": 1,
    "F2-related_disorder|Prolonged_prothrombin_time|Ischemic_stroke|Pregnancy_loss|_recurrent|_susceptibility_to|_2|Congenital_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect|not_provided": 1,
    "Inborn_genetic_diseases|Thrombophilia_due_to_thrombin_defect|not_specified|not_provided|Congenital_prothrombin_deficiency": 1,
    "Thrombophilia_due_to_thrombin_defect|F2-related_disorder|not_provided": 1,
    "Venous_thromboembolism|Thrombophilia_caused_by_F2_prothrombin_deficiency|Thrombophilia_due_to_thrombin_defect|Pregnancy_loss|_recurrent|_susceptibility_to|_2|Ischemic_stroke|Congenital_prothrombin_deficiency|not_provided|Cerebral_palsy": 1,
    "Cenani-Lenz_syndactyly_syndrome": 67,
    "Cenani-Lenz_syndactyly_syndrome|not_provided": 3,
    "not_provided|Cenani-Lenz_syndactyly_syndrome": 4,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2": 234,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 136,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 246,
    "LRP4-related_disorder": 13,
    "not_provided|Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 2,
    "Cenani-Lenz_syndactyly_syndrome|Meniere_disease|LRP4-related_disorder|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_provided": 1,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases": 8,
    "not_specified|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome": 1,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Inborn_genetic_diseases": 6,
    "Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 91,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|LRP4-related_disorder": 8,
    "Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome": 45,
    "Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2": 147,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2": 10,
    "not_provided|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases": 2,
    "not_specified|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2": 3,
    "LRP4-related_disorder|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|not_provided": 2,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_provided|Inborn_genetic_diseases": 1,
    "LRP4-related_disorder|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 5,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|not_provided": 3,
    "not_provided|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2": 4,
    "Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Inborn_genetic_diseases": 14,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|not_specified": 2,
    "Inborn_genetic_diseases|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 5,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_provided": 15,
    "not_specified|LRP4-related_disorder|not_provided|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2": 1,
    "not_provided|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 10,
    "Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|LRP4-related_disorder": 2,
    "not_provided|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases": 1,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases": 9,
    "not_provided|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 8,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 16,
    "Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|not_provided": 6,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|not_provided": 1,
    "LRP4-related_disorder|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome": 1,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 5,
    "Sclerosteosis_2|not_provided|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 1,
    "Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|not_provided|Inborn_genetic_diseases|LRP4-related_disorder": 1,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|not_provided": 12,
    "not_provided|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2": 3,
    "not_provided|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Meniere_disease": 1,
    "Sclerosteosis_2": 2,
    "Isolated_hand_syndactyly": 2,
    "LRP4-related_disorder|Bone_Mineral_Density_Variation|not_provided|not_specified|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 1,
    "Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome": 3,
    "Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|not_specified": 2,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_provided": 1,
    "Inborn_genetic_diseases|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome": 1,
    "not_provided|LRP4-related_disorder|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2": 1,
    "not_provided|not_specified|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases": 1,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_specified|not_provided": 1,
    "not_provided|LRP4-related_disorder|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases": 1,
    "Sclerosteosis_2|not_provided|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 1,
    "Cenani-Lenz_syndactyly_syndrome|LRP4-related_disorder|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 1,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|not_provided|LRP4-related_disorder|not_specified": 1,
    "Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|not_provided": 4,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|not_provided|Sclerosteosis_2": 1,
    "LRP4-related_disorder|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2": 2,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|LRP4-related_disorder": 2,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 1,
    "Epilepsy|Inborn_genetic_diseases|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 1,
    "Sclerosteosis_2|not_specified|not_provided|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 2,
    "LRP4-related_disorder|not_provided": 2,
    "not_provided|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Inborn_genetic_diseases": 1,
    "LRP4-related_disorder|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|not_provided": 1,
    "Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Inborn_genetic_diseases": 5,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_specified|LRP4-related_disorder|not_provided": 1,
    "Cenani-Lenz_syndactyly_syndrome|Inborn_genetic_diseases|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 1,
    "Congenital_myasthenic_syndrome_17": 2,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|LRP4-related_disorder|not_provided": 2,
    "not_specified|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|LRP4-related_disorder": 1,
    "not_specified|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Inborn_genetic_diseases": 1,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2": 1,
    "LRP4-related_disorder|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_provided": 2,
    "not_specified|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 1,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|not_provided": 2,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Intellectual_disability|not_provided": 1,
    "Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|LRP4-related_disorder": 1,
    "Sclerosteosis_2|not_specified|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|not_provided": 1,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|not_specified|not_provided": 1,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|LRP4-related_disorder|not_provided|not_specified": 1,
    "not_provided|LRP4-related_disorder|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome": 1,
    "Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Inborn_genetic_diseases|Meniere_disease": 1,
    "Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|Sclerosteosis_2": 1,
    "LRP4-related_disorder|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 1,
    "not_provided|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|LRP4-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17": 1,
    "Cenani-Lenz_syndactyly_syndrome|not_provided|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_specified": 1,
    "Cenani-Lenz_syndactyly_syndrome|not_provided|not_specified": 1,
    "not_provided|Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Inborn_genetic_diseases": 1,
    "Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Meniere_disease": 1,
    "Inborn_genetic_diseases|Cenani-Lenz_syndactyly_syndrome": 1,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_specified": 2,
    "not_specified|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome": 1,
    "Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17|LRP4-related_disorder": 1,
    "Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|not_provided|LRP4-related_disorder": 1,
    "Congenital_myasthenic_syndrome_17|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Inborn_genetic_diseases|Intellectual_disability|not_provided": 1,
    "not_specified|Cenani-Lenz_syndactyly_syndrome|Sclerosteosis_2|Congenital_myasthenic_syndrome_17|LRP4-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|LRP4-related_disorder|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|Congenital_myasthenic_syndrome_17": 1,
    "Congenital_myasthenic_syndrome_17|Sclerosteosis_2|Cenani-Lenz_syndactyly_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Bone_Mineral_Density_Variation": 1,
    "ARFGAP2-related_disorder": 14,
    "CONGENITAL_MYOPATHY_27": 3,
    "Xeroderma_pigmentosum|_group_E": 30,
    "Xeroderma_pigmentosum|_group_E|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_E": 1,
    "not_specified|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_E|not_provided": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_E": 2,
    "Xeroderma_pigmentosum|_group_E|not_provided|Xeroderma_pigmentosum": 2,
    "Xeroderma_pigmentosum|_group_E|Inborn_genetic_diseases": 2,
    "DDB2-related_disorder|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|_group_E": 7,
    "Xeroderma_pigmentosum|_group_E|Xeroderma_pigmentosum": 1,
    "not_specified|Xeroderma_pigmentosum|_group_E": 1,
    "DDB2-related_disorder|not_specified|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_E": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia": 8,
    "Deeah_syndrome": 10,
    "MADD-related_disorder|not_provided": 1,
    "MADD-related_disorder": 22,
    "not_provided|MADD-related_disorder": 7,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|not_provided|MADD-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|Deeah_syndrome": 3,
    "Deeah_syndrome|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia": 2,
    "Deeah_syndrome|MADD-related_disorder": 2,
    "Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|Deeah_syndrome": 6,
    "MADD-related_disorder|Deeah_syndrome|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|not_provided": 1,
    "MADD-related_disorder|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|Deeah_syndrome": 1,
    "Inborn_genetic_diseases|Deeah_syndrome|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia": 1,
    "MADD-related_disorder|not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|Deeah_syndrome": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|Deeah_syndrome": 1,
    "Deeah_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deeah_syndrome": 2,
    "MADD-related_disorder|Inborn_genetic_diseases": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|_severe_neonatal_type": 1,
    "Inborn_genetic_diseases|MADD-related_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies|_impaired_speech|_and_hypotonia|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 13,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 5,
    "not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 8,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 9,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 4,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 7,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 18,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_1MM|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided|Left_ventricular_noncompaction_10|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 8,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 27,
    "Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Asymmetric_septal_hypertrophy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 5,
    "Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Hypertrophic_cardiomyopathy": 3,
    "Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Left_ventricular_noncompaction_10|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_4|not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 7,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 16,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 11,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 13,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4": 2,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 5,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1I|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|See_cases|Left_ventricular_hypertrophy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 4,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "MYBPC3-related_disorder|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 4,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 10,
    "MYBPC3-related_disorder|Left_ventricular_noncompaction_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 20,
    "Cardiomyopathy|_familial_hypertrophic|_4|_susceptibility_to": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Peripheral_neuropathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 4,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 2,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 6,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 5,
    "not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiomyopathy": 3,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 24,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 7,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 8,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 10,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided|MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_specified|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 11,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|Brugada_syndrome|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 7,
    "not_provided|not_specified|Left_ventricular_noncompaction_10|Cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrest|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 6,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided": 2,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy|Primary_familial_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "not_specified|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 2,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|MYBPC3-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 26,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 4,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|MYBPC3-related_disorder": 1,
    "Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 10,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 10,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Premature_ventricular_contraction|Noncompaction_cardiomyopathy|Tachycardia|Asymmetric_septal_hypertrophy|Dyspnea|Heart_block|MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 3,
    "MYBPC3-related_disorder": 6,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 4,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 18,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 5,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Concentric_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 2,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 7,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 10,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 5,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Long_QT_syndrome": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy": 6,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 2,
    "not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 3,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|not_specified": 2,
    "not_provided|MYBPC3-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 2,
    "Cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy": 14,
    "Left_ventricular_noncompaction_10": 4,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1A": 1,
    "not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Left_ventricular_noncompaction_10|Paroxysmal_atrial_fibrillation|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 2,
    "not_specified|not_provided|Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 4,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiomyopathy|Cardiomyopathy|_dilated|_1MM": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 2,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Prolonged_QT_interval|not_specified|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|not_provided|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 4,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_specified|not_provided|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 5,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Brugada_syndrome|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy": 2,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 6,
    "MYBPC3-related_disorder|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Long_QT_syndrome|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|MYBPC3-related_disorder|Left_ventricular_noncompaction_10|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "Inborn_genetic_diseases|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 2,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 2,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|not_specified|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_specified": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_provided": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 7,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10": 3,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_dilated|_1MM|Left_ventricular_noncompaction_10|Paroxysmal_atrial_fibrillation|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 3,
    "Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 16,
    "Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 3,
    "Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy_4|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 3,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Dilated_cardiomyopathy_1A": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 9,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 2,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 3,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 6,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|not_specified": 13,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 3,
    "Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided|Left_ventricular_noncompaction_10|not_specified": 1,
    "MYBPC3-related_disorder|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|not_provided": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|not_specified|Left_ventricular_noncompaction_10|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_provided|See_cases|Cardiomyopathy": 1,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_4|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified": 14,
    "not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 2,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4": 1,
    "MYBPC3-related_disorder|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype": 2,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy_1|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "MYBPC3-related_disorder|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1": 18,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|not_specified": 3,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Left_ventricular_noncompaction_10": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 7,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_specified|not_provided|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "MYBPC3-related_cardiomyopathies|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 11,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 5,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|Heart_failure|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 2,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Hypertrophic_cardiomyopathy|not_provided": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Amyloidosis|_hereditary_systemic_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 3,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|See_cases|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_1MM|MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 4,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|MYBPC3-related_disorder|not_provided|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_4|Isolated_Noncompaction_of_the_Ventricular_Myocardium": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy_1": 2,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Mitochondrial_disease|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 2,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 5,
    "See_cases|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "MYBPC3-related_disorder|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiomyopathy|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiomyopathy|MYBPC3-related_disorder": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|not_specified|not_provided|Hypertrophic_cardiomyopathy_4": 2,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Wolff-Parkinson-White_pattern|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|MYBPC3-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_specified|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_1|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 9,
    "not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|MYBPC3-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Left_ventricular_noncompaction": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_provided|not_specified|See_cases|Cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 1,
    "not_provided|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_provided": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Premature_ventricular_contraction|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_4": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "not_specified|MYBPC3-related_disorder|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy_4|MYBPC3-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 2,
    "not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided": 17,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|SUDDEN_INFANT_DEATH_SYNDROME|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Long_QT_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 7,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|MYBPC3-related_disorder": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Abnormality_of_the_cardiovascular_system|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "MYBPC3-related_disorder|not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Asymmetric_septal_hypertrophy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided|not_specified": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_specified|Left_ventricular_noncompaction_10|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|See_cases|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|not_specified": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|not_specified": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiomyopathy|Cardiovascular_phenotype|MYBPC3-related_disorder|not_provided": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified": 1,
    "hyprtrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction_10|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4": 1,
    "Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10": 1,
    "Aganglionic_megacolon|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1A|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_10|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "MYBPC3-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy": 1,
    "Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Long_QT_syndrome": 1,
    "not_provided|Left_ventricular_noncompaction_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided": 8,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy_4|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "not_specified|MYBPC3-related_disorder|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy_4|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|MYBPC3-related_disorder|Left_ventricular_noncompaction_10": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_specified|Cardiomyopathy|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Long_QT_syndrome|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|MYBPC3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "Hypertrophic_cardiomyopathy_4|not_specified|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|not_provided|MYBPC3-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|MYBPC3-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_10|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|MYBPC3-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYBPC3-related_disorder|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Intellectual_disability": 1,
    "MYBPC3-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_4|Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_hypertrophy|Hypertrophic_cardiomyopathy": 1,
    "MYBPC3-related_disorder|Hypertrophic_cardiomyopathy_4|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_10|Hypertrophic_cardiomyopathy_4|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Agammaglobulinemia": 115,
    "SPI1-related_condition": 1,
    "Agammaglobulinemia|not_specified": 3,
    "PU.1-mutated_agammaglobulinemia|Agammaglobulinemia|Agammaglobulinemia_10|_autosomal_dominant": 1,
    "Agammaglobulinemia|PU.1-mutated_agammaglobulinemia|Agammaglobulinemia_10|_autosomal_dominant": 3,
    "not_provided|Agammaglobulinemia_10|_autosomal_dominant": 1,
    "Agammaglobulinemia_10|_autosomal_dominant": 2,
    "not_specified|Agammaglobulinemia": 6,
    "PU.1-mutated_agammaglobulinemia": 1,
    "Agammaglobulinemia_10|_autosomal_dominant|Agammaglobulinemia": 1,
    "Agammaglobulinemia|Agammaglobulinemia_10|_autosomal_dominant|not_provided|PU.1-mutated_agammaglobulinemia": 1,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 184,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 7,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 19,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_specified": 4,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided": 14,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided|not_specified": 4,
    "not_specified|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 6,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 3,
    "not_specified|Ehlers-Danlos_syndrome|Connective_tissue_disorder|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|SLC39A13-related_disorder": 2,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Inborn_genetic_diseases|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_provided|SLC39A13-related_disorder|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_specified|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided": 2,
    "not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_specified": 2,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Inborn_genetic_diseases": 1,
    "Connective_tissue_disorder|SLC39A13-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Mitral_valve_prolapse|Cutis_laxa|Myopia|Abnormality_of_connective_tissue|Scleroderma|Abnormality_of_the_skeletal_system": 1,
    "Inborn_genetic_diseases|not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "SLC39A13-related_disorder|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_provided|not_specified|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_specified|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "SLC39A13-related_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_specified|not_provided|SLC39A13-related_disorder|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "Connective_tissue_disorder|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Ehlers-Danlos_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Ehlers-Danlos_syndrome": 1,
    "not_specified|SLC39A13-related_disorder|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided|Connective_tissue_disorder": 1,
    "not_specified|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|Connective_tissue_disorder": 1,
    "SLC39A13-related_disorder|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided|Connective_tissue_disorder": 1,
    "SLC39A13-related_disorder|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 2,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided|SLC39A13-related_disorder": 1,
    "not_provided|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|SLC39A13-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided|Inborn_genetic_diseases": 1,
    "SLC39A13-related_disorder|Connective_tissue_disorder|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type": 1,
    "Ehlers-Danlos_syndrome|_spondylocheirodysplastic_type|not_provided|Connective_tissue_disorder|Ehlers-Danlos_syndrome": 1,
    "Deafness|_cataract|_impaired_intellectual_development|_and_polyneuropathy|Neurodevelopmental_delay|Severe_sensorineural_hearing_impairment|Developmental_cataract": 1,
    "Patent_ductus_arteriosus|Atrial_septal_defect|_ostium_secundum_type|Developmental_dysplasia_of_the_hip|Abnormality_of_the_pulmonary_veins|Microcephaly|Patent_foramen_ovale|Global_developmental_delay|High_anterior_hairline|Microretrognathia|Failure_to_thrive|Polymicrogyria|Cerebellar_vermis_hypoplasia": 1,
    "PSMC3-Related_Neurodevelopmental_Delay": 1,
    "Congenital_Myasthenic_Syndrome|_Recessive|Fetal_akinesia_deformation_sequence_1": 4,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 203,
    "Congenital_myasthenic_syndrome_11|not_provided|Fetal_akinesia_deformation_sequence_1": 2,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|not_provided|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 194,
    "not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 5,
    "Fetal_akinesia_deformation_sequence_2": 13,
    "RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_provided|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_11|not_provided|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 16,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 2,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided|Congenital_myasthenic_syndrome": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Inborn_genetic_diseases|Congenital_myasthenic_syndrome": 1,
    "RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2|not_provided": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|not_specified": 1,
    "RAPSN-related_disorder": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_provided": 7,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 5,
    "Hydrops_fetalis": 4,
    "Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_specified|Congenital_myasthenic_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 2,
    "Congenital_myasthenic_syndrome|not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_1": 1,
    "not_specified|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_2": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|not_provided|Fetal_akinesia_deformation_sequence_2": 1,
    "Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2": 2,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2|Inborn_genetic_diseases|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome": 13,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2": 7,
    "Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 6,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided|not_specified|Fetal_akinesia_deformation_sequence_2": 1,
    "Congenital_myasthenic_syndrome|not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 1,
    "Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 8,
    "Congenital_myasthenic_syndrome|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1": 2,
    "not_provided|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 2,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2": 1,
    "Congenital_myasthenic_syndrome_11": 6,
    "Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|RAPSN-related_disorder|not_specified": 1,
    "not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome": 3,
    "Congenital_myasthenic_syndrome_11|Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 1,
    "not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_specified": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_specified": 2,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|RAPSN-related_disorder": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 4,
    "RAPSN-related_disorder|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_11|not_provided|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1": 1,
    "not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome": 2,
    "RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided|Global_developmental_delay": 1,
    "Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Inborn_genetic_diseases": 3,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 1,
    "RAPSN-related_disorder|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 2,
    "Fetal_akinesia_deformation_sequence_2|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 3,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_specified": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_provided|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_specified": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1": 3,
    "Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 3,
    "Congenital_Myasthenic_Syndrome|_Recessive|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_provided": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|RAPSN-related_disorder": 1,
    "Fetal_akinesia_deformation_sequence_2|Congenital_Myasthenic_Syndrome|_Recessive|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|not_specified|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2": 1,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|not_provided": 1,
    "RAPSN-related_disorder|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases": 1,
    "Fetal_akinesia_deformation_sequence_2|not_specified": 1,
    "not_specified|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2": 3,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 2,
    "not_specified|Fetal_akinesia_deformation_sequence_2": 1,
    "RAPSN-related_disorder|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome": 2,
    "RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 2,
    "Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_11|RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2|Myopathy": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_1": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 2,
    "not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_specified": 1,
    "Congenital_myasthenic_syndrome_11|not_specified|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1": 1,
    "Inborn_genetic_diseases|not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2|RAPSN-related_disorder|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_2|not_provided|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_provided|Fetal_akinesia_deformation_sequence_2|Inborn_genetic_diseases": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2": 1,
    "RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_2|not_specified|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_provided": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Arthrogryposis_multiplex_congenita": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1|not_provided|Congenital_myasthenic_syndrome": 1,
    "RAPSN-related_disorder|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided|Myopathy|Congenital_myasthenic_syndrome_4C": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|RAPSN-related_disorder": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|not_specified|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Inborn_genetic_diseases|not_provided": 1,
    "RAPSN-related_disorder|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "Inborn_genetic_diseases|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2|not_provided": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2": 1,
    "Fetal_akinesia_deformation_sequence_2|not_provided|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2|not_provided": 1,
    "Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_specified|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome|Hydrops_fetalis": 1,
    "Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome_11|not_provided|Fetal_akinesia_deformation_sequence_2": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome": 10,
    "Fetal_akinesia_deformation_sequence_2|not_provided|Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1": 1,
    "Fetal_akinesia_deformation_sequence_1|Fetal_akinesia_deformation_sequence_2|Congenital_myasthenic_syndrome_11": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|Fetal_akinesia_deformation_sequence_2": 1,
    "Congenital_myasthenic_syndrome_11|Fetal_akinesia_deformation_sequence_2|Fetal_akinesia_deformation_sequence_1|Congenital_myasthenic_syndrome|Abnormality_of_the_musculature": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_ATAXIA_AND_BRAIN_ABNORMALITIES": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_8": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|NDUFS3-related_disorder": 4,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided|Leigh_syndrome": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_8": 2,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_8|not_provided": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_8|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_8": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_8|Neurodevelopmental_delay": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFS3-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_8|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_8|not_specified|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_8|not_provided": 1,
    "NDUFS3-related_disorder|not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_8": 1,
    "NDUFS3-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "Abnormal_brain_morphology|Epilepsy": 1,
    "FNBP4-related_disorder": 3,
    "Nephrotic_syndrome|_type_19": 9,
    "not_provided|NUP160-related_disorder": 11,
    "NUP160-related_disorder|not_provided": 7,
    "Nephrotic_syndrome|_type_19|not_specified": 1,
    "NUP160-related_disorder": 18,
    "not_specified|NUP160-related_disorder": 1,
    "not_provided|Nephrotic_syndrome|_type_19": 1,
    "not_provided|NUP160-related_disorder|Nephrotic_syndrome|_type_19": 1,
    "PTPRJ-related_disorder": 30,
    "Thrombocytopenia_10": 2,
    "PTPRJ-related_disorder|not_specified": 2,
    "Carcinoma_of_colon|Colorectal_cancer|not_provided|PTPRJ-related_disorder|not_specified": 1,
    "not_provided|PTPRJ-related_disorder": 1,
    "OR4P4-related_disorder": 2,
    "SERPING1-related_disorder": 6,
    "Hereditary_angioedema_type_1": 235,
    "Hereditary_angioneurotic_edema": 1,
    "SERPING1-related_disorder|Hereditary_angioedema_type_1": 3,
    "Hereditary_angioedema_type_1|SERPING1-related_disorder": 1,
    "not_specified|Hereditary_angioedema_type_1|not_provided": 1,
    "not_provided|Hereditary_angioedema_type_1": 30,
    "C1_inhibitor_deficiency|Hereditary_angioedema_type_1|not_provided": 1,
    "not_provided|SERPING1-related_disorder": 5,
    "Angioedema": 11,
    "Hereditary_angioedema_type_1|not_provided": 18,
    "Angioedema|not_provided": 1,
    "Hereditary_angioedema_with_C1Inh_deficiency": 30,
    "Hereditary_angioedema_type_1|C1_inhibitor_deficiency": 3,
    "SERPING1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "SERPING1-related_disorder|not_provided": 2,
    "not_provided|Hereditary_angioedema_type_1|C1_inhibitor_deficiency": 3,
    "not_provided|Inborn_genetic_diseases|SERPING1-related_disorder": 1,
    "not_provided|SERPING1-related_disorder|Hereditary_angioedema_type_1": 1,
    "SERPING1-related_disorder|Hereditary_angioedema_type_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_angioedema_type_1": 1,
    "not_provided|SERPING1-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_angioedema_type_1|not_specified|not_provided": 2,
    "not_provided|Angioedema": 2,
    "Inborn_genetic_diseases|Hereditary_angioedema_type_1|not_provided": 2,
    "Hereditary_angioedema_type_1|Hereditary_angioedema_with_C1Inh_deficiency": 4,
    "not_provided|Hereditary_angioedema_type_1|SERPING1-related_disorder": 1,
    "Angioedema|Hereditary_angioedema_type_1": 1,
    "Inborn_genetic_diseases|SERPING1-related_disorder|not_provided": 1,
    "Hereditary_angioedema_type_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_angioedema_type_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "SERPING1-related_disorder|Inborn_genetic_diseases|Hereditary_angioedema_type_1": 1,
    "Hereditary_angioedema_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_angioedema_with_C1Inh_deficiency|not_provided": 1,
    "C1_inhibitor_deficiency|not_provided": 1,
    "not_specified|not_provided|Hereditary_angioedema_type_1": 1,
    "Hereditary_C1_esterase_inhibitor_deficiency_-_dysfunctional_factor": 3,
    "Complement_component_4|_partial_deficiency_of|_due_to_dysfunctional_c1_inhibitor|not_provided": 1,
    "Hereditary_C1_esterase_inhibitor_deficiency_-_dysfunctional_factor|not_provided": 1,
    "not_provided|Hereditary_angioedema_type_1|Hereditary_C1_esterase_inhibitor_deficiency_-_dysfunctional_factor": 1,
    "Hereditary_angioedema_type_1|Hereditary_C1_esterase_inhibitor_deficiency_-_dysfunctional_factor|not_provided|Inborn_genetic_diseases|C1_inhibitor_deficiency": 1,
    "Hereditary_angioedema_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_angioedema_type_1": 1,
    "Pontocerebellar_hypoplasia_type_10|not_specified": 1,
    "Pontocerebellar_hypoplasia_type_10": 9,
    "Pontocerebellar_hypoplasia_type_10|Inborn_genetic_diseases": 2,
    "not_provided|CLP1-related_disorder": 2,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_10|not_provided": 1,
    "not_specified|not_provided|CLP1-related_disorder": 1,
    "CLP1-related_disorder|not_provided": 1,
    "not_provided|CLP1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_microcephaly|_cortical_malformations|_and_spasticity": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_cortical_malformations|_and_spasticity": 11,
    "TMX2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TMX2-related_disorder": 3,
    "Abnormality_of_the_nervous_system|Neurodevelopmental_disorder_with_microcephaly|_cortical_malformations|_and_spasticity|not_provided": 1,
    "not_provided|TMX2-related_disorder": 1,
    "CTNND1-related_disorder": 18,
    "not_provided|Cleft_lip_with_or_without_cleft_palate": 2,
    "Inborn_genetic_diseases|CTNND1-related_disorder": 1,
    "not_provided|CTNND1-related_disorder": 4,
    "not_provided|Blepharocheilodontic_syndrome_2": 3,
    "Blepharocheilodontic_syndrome_2": 16,
    "Blepharocheilodontic_syndrome_2|Inborn_genetic_diseases": 2,
    "Cleft_lip_with_or_without_cleft_palate|not_provided": 1,
    "Inborn_genetic_diseases|Blepharocheilodontic_syndrome_2": 1,
    "Cleft_lip_with_or_without_cleft_palate|Blepharocheilodontic_syndrome_2": 1,
    "CTNND1-related_disorder|not_provided": 1,
    "not_provided|CILIARY_NEUROTROPHIC_FACTOR_POLYMORPHISM": 1,
    "FAM111B-related_disorder": 7,
    "Inborn_genetic_diseases|Hereditary_sclerosing_poikiloderma_with_tendon_and_pulmonary_involvement": 2,
    "not_specified|Hereditary_sclerosing_poikiloderma_with_tendon_and_pulmonary_involvement": 1,
    "Hereditary_sclerosing_poikiloderma_with_tendon_and_pulmonary_involvement|not_provided": 2,
    "Hereditary_sclerosing_poikiloderma_with_tendon_and_pulmonary_involvement": 13,
    "not_provided|Hereditary_sclerosing_poikiloderma_with_tendon_and_pulmonary_involvement": 1,
    "FAM111B-related_disorder|Inborn_genetic_diseases": 1,
    "FAM111A-related_disorder|not_provided": 3,
    "FAM111A-related_disorder": 7,
    "not_provided|See_cases|FAM111A-related_disorder": 1,
    "not_provided|Osteocraniostenosis|Autosomal_dominant_Kenny-Caffey_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|FAM111A-related_disorder": 3,
    "Osteocraniostenosis": 6,
    "FAM111A-related_disorder|not_provided|Autosomal_dominant_Kenny-Caffey_syndrome|not_specified": 1,
    "FAM111A-related_disorder|not_specified|not_provided": 1,
    "Autosomal_dominant_Kenny-Caffey_syndrome|Osteocraniostenosis": 1,
    "Inborn_genetic_diseases|Osteocraniostenosis|Autosomal_dominant_Kenny-Caffey_syndrome": 1,
    "not_provided|Autosomal_dominant_Kenny-Caffey_syndrome|Osteocraniostenosis": 2,
    "FAM111A-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_Kenny-Caffey_syndrome": 3,
    "Hypoparathyroidism|not_provided": 1,
    "not_provided|Osteocraniostenosis": 1,
    "Autosomal_dominant_Kenny-Caffey_syndrome|Osteocraniostenosis|not_provided|Inborn_genetic_diseases": 1,
    "Immunodeficiency_77": 16,
    "Immunodeficiency_77|MPEG1-related_immunodeficiency": 1,
    "Immunodeficiency_77|not_provided": 2,
    "MPEG1-related_disorder": 2,
    "Castleman-Kojima_disease": 4,
    "OSBP-related_disorder|not_provided": 2,
    "OSBP-related_disorder": 6,
    "Retinal_dystrophy_and_microvillus_inclusion_disease": 3,
    "Retinal_dystrophy_and_microvillus_inclusion_disease|not_provided": 1,
    "STX3-related_disorder|not_provided": 3,
    "not_provided|STX3-related_disorder": 3,
    "Diarrhea_12|_with_microvillus_atrophy|not_provided": 1,
    "Hereditary_intrinsic_factor_deficiency": 90,
    "not_specified|Hereditary_intrinsic_factor_deficiency": 9,
    "Hereditary_intrinsic_factor_deficiency|not_specified": 9,
    "CBLIF-related_disorder|Hereditary_intrinsic_factor_deficiency": 2,
    "not_provided|Hereditary_intrinsic_factor_deficiency": 4,
    "CBLIF-related_disorder": 1,
    "not_specified|CBLIF-related_disorder|Hereditary_intrinsic_factor_deficiency": 1,
    "Hereditary_intrinsic_factor_deficiency|not_specified|not_provided": 1,
    "not_provided|CBLIF-related_disorder|Hereditary_intrinsic_factor_deficiency": 2,
    "CBLIF-related_disorder|not_provided|Hereditary_intrinsic_factor_deficiency": 1,
    "CBLIF-related_disorder|Hereditary_intrinsic_factor_deficiency|not_provided": 1,
    "Hereditary_intrinsic_factor_deficiency|not_provided": 1,
    "CBLIF-related_disorder|not_specified|not_provided|Hereditary_intrinsic_factor_deficiency": 1,
    "Hereditary_intrinsic_factor_deficiency|See_cases|not_provided": 1,
    "not_provided|Intrinsic_factor_deficiency|_congenital|_susceptibility_to|Hereditary_intrinsic_factor_deficiency": 1,
    "Hereditary_intrinsic_factor_deficiency|CBLIF-related_disorder": 1,
    "not_specified|Transcobalamin_I_deficiency": 7,
    "Transcobalamin_I_deficiency": 83,
    "TCN1-related_disorder": 3,
    "Transcobalamin_I_deficiency|TCN1-related_disorder": 3,
    "Transcobalamin_I_deficiency|not_specified": 9,
    "Transcobalamin_I_deficiency|not_provided": 2,
    "not_specified|not_provided|Transcobalamin_I_deficiency": 2,
    "not_provided|Transcobalamin_I_deficiency": 4,
    "TCN1-related_disorder|not_provided|Transcobalamin_I_deficiency": 1,
    "not_specified|Transcobalamin_I_deficiency|not_provided": 1,
    "TCN1-related_disorder|Transcobalamin_I_deficiency": 2,
    "MS4A2-related_disorder": 4,
    "RECLASSIFIED_-_MYOC_POLYMORPHISM": 3,
    "Immunodeficiency|_common_variable|_5": 2,
    "not_provided|Immunodeficiency|_common_variable|_5": 2,
    "not_specified|Immunodeficiency|_common_variable|_5": 1,
    "Immunodeficiency|_common_variable|_5|not_provided": 3,
    "MS4A1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_5": 1,
    "MS4A1-related_disorder": 2,
    "not_provided|MS4A1-related_disorder": 1,
    "Female_infertility_due_to_zona_pellucida_defect": 12,
    "ZP1-related_disorder|not_provided": 2,
    "Female_infertility_due_to_zona_pellucida_defect|ZP1-related_disorder": 1,
    "ZP1-related_disorder": 2,
    "CD6-related_disorder": 15,
    "DDB1-related_disorder": 8,
    "White-Kernohan_syndrome": 14,
    "not_provided|White-Kernohan_syndrome": 1,
    "not_provided|not_specified|White-Kernohan_syndrome": 1,
    "Triokinase_and_FMN_cyclase_deficiency_syndrome": 2,
    "not_provided|Triokinase_and_FMN_cyclase_deficiency_syndrome": 5,
    "not_specified|Triokinase_and_FMN_cyclase_deficiency_syndrome": 1,
    "TKFC_deficiency|Inborn_errors_of_metabolism|Triokinase_and_FMN_cyclase_deficiency_syndrome": 2,
    "TKFC-related_disorder": 1,
    "Joubert_syndrome_16": 120,
    "TMEM138-related_disorder": 1,
    "not_specified|Joubert_syndrome_16": 2,
    "Joubert_syndrome_16|not_specified|not_provided": 1,
    "not_provided|Joubert_syndrome_16": 8,
    "Joubert_syndrome_16|not_provided": 3,
    "not_provided|Joubert_syndrome_16|Joubert_syndrome_and_related_disorders": 1,
    "TMEM138-related_disorder|Joubert_syndrome_16": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_16": 6,
    "Joubert_syndrome_16|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_16": 2,
    "Joubert_syndrome_16|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Joubert_syndrome_16": 1,
    "not_provided|TMEM138-related_disorder|Joubert_syndrome_16": 1,
    "Joubert_syndrome_16|TMEM138-related_disorder": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_16": 1,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2": 26,
    "not_provided|Meckel_syndrome|_type_2|Joubert_syndrome_2": 2,
    "Retinitis_pigmentosa_98|not_provided": 1,
    "TMEM216-related_disorder": 3,
    "not_specified|Meckel_syndrome|_type_2|Joubert_syndrome_2|not_provided": 1,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2|not_specified|TMEM216-related_disorder": 1,
    "Meckel_syndrome|_type_2|not_specified|Joubert_syndrome|Joubert_syndrome_2|not_provided": 1,
    "Joubert_syndrome|Meckel_syndrome|_type_2|Joubert_syndrome_2": 3,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2|Joubert_syndrome": 6,
    "Meckel_syndrome|_type_2|not_provided|Joubert_syndrome|Joubert_syndrome_2|TMEM216-related_disorder": 1,
    "not_provided|Joubert_syndrome|Joubert_syndrome_2|Meckel_syndrome|_type_2": 1,
    "Joubert_syndrome_2": 17,
    "Joubert_syndrome_2|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_2|Meckel_syndrome|_type_2|Inborn_genetic_diseases|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2|Inborn_genetic_diseases|Joubert_syndrome": 1,
    "Joubert_syndrome_2|Inborn_genetic_diseases|Joubert_syndrome": 2,
    "Joubert_syndrome|not_provided|Meckel_syndrome|_type_2|Joubert_syndrome_2": 1,
    "Joubert_syndrome_2|not_specified|not_provided|Meckel_syndrome|_type_2|Joubert_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_2|not_provided|Meckel_syndrome|_type_2": 1,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2|Joubert_syndrome|Retinitis_pigmentosa_98": 1,
    "Joubert_syndrome|Joubert_syndrome_2": 4,
    "Joubert_syndrome|Joubert_syndrome_2|TMEM216-related_disorder|Meckel_syndrome|_type_2|not_provided": 1,
    "Joubert_syndrome_2|Meckel_syndrome|_type_2|not_provided|Joubert_syndrome": 1,
    "Retinitis_pigmentosa_98|Joubert_syndrome": 1,
    "Joubert_syndrome_2|Joubert_syndrome": 6,
    "Joubert_syndrome_2|Meckel_syndrome|_type_2": 15,
    "Joubert_syndrome|Joubert_syndrome_2|Meckel_syndrome|_type_2|TMEM216-related_disorder|not_provided": 1,
    "TMEM216-related_disorder|Joubert_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_2|not_provided|TMEM216-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_2|Meckel_syndrome|_type_2": 4,
    "Retinal_dystrophy|Joubert_syndrome_2|Meckel_syndrome|_type_2|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome_2|not_provided": 1,
    "not_specified|Joubert_syndrome|Joubert_syndrome_2": 1,
    "Joubert_syndrome|not_specified|Meckel_syndrome|_type_2|Joubert_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Joubert_syndrome|Joubert_syndrome_2|Abnormality_of_the_nervous_system": 1,
    "Joubert_syndrome_2|Meckel_syndrome|_type_2|Joubert_syndrome": 1,
    "Joubert_syndrome_2|Meckel_syndrome|_type_2|TMEM216-related_disorder|Inborn_genetic_diseases|not_provided|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_2|Meckel_syndrome|_type_2": 1,
    "Meckel_syndrome|_type_2": 2,
    "not_provided|Joubert_syndrome_2|not_specified|Joubert_syndrome|Meckel_syndrome|_type_2": 1,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2|TMEM216-related_disorder|not_provided|Joubert_syndrome": 2,
    "Joubert_syndrome|not_provided|Meckel_syndrome|_type_2|Joubert_syndrome_2|not_specified": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_2|Joubert_syndrome_2": 2,
    "not_provided|Retinal_dystrophy|Joubert_syndrome|Meckel_syndrome|_type_2|Joubert_syndrome_2": 1,
    "Joubert_syndrome|Joubert_syndrome_2|not_provided": 1,
    "not_specified|Joubert_syndrome|not_provided|Meckel_syndrome|_type_2|Joubert_syndrome_2|Inborn_genetic_diseases": 1,
    "not_specified|Joubert_syndrome|not_provided|Meckel_syndrome|_type_2|TMEM216-related_disorder|Inborn_genetic_diseases|Joubert_syndrome_2": 1,
    "not_provided|Joubert_syndrome_2|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "TMEM216-related_disorder|Meckel_syndrome|_type_2|Joubert_syndrome_2|not_provided|Joubert_syndrome": 1,
    "Joubert_syndrome|Joubert_syndrome_2|TMEM216-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_2|Meckel_syndrome|_type_2|not_provided": 1,
    "not_provided|Joubert_syndrome|Meckel_syndrome|_type_2|Joubert_syndrome_2": 1,
    "not_specified|Meckel_syndrome|_type_2": 1,
    "not_specified|not_provided|Joubert_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome|Meckel_syndrome|_type_2|Joubert_syndrome_2|Joubert_syndrome_1|not_specified": 1,
    "TMEM216-related_disorder|Joubert_syndrome_2|not_provided": 1,
    "not_specified|not_provided|Meckel_syndrome|_type_2|Joubert_syndrome_2": 1,
    "Meckel_syndrome|_type_2|Joubert_syndrome_2|not_provided": 1,
    "not_specified|Hereditary_pheochromocytoma-paraganglioma": 3,
    "SDHAF2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_2": 2,
    "Hereditary_pheochromocytoma-paraganglioma|SDHAF2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_2|SDHAF2-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 6,
    "SDHAF2-related_disorder|Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2": 6,
    "Hereditary_cancer-predisposing_syndrome|SDHAF2-related_disorder|not_provided|Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2": 7,
    "Pheochromocytoma/paraganglioma_syndrome_2": 7,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Ovarian_cancer": 1,
    "Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_2": 2,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2": 3,
    "not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|SDHAF2-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_pheochromocytoma-paraganglioma|SDHAF2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Ovarian_cancer|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_2|SDHAF2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|SDHAF2-related_disorder|not_specified|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 3,
    "Hereditary_pheochromocytoma-paraganglioma|not_specified|not_provided": 2,
    "SDHAF2-related_disorder|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_2|Hereditary_pheochromocytoma-paraganglioma": 1,
    "SDHAF2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_2": 1,
    "DAGLA-related_disorder": 18,
    "not_provided|DAGLA-related_disorder": 3,
    "Benign_paroxysmal_tonic_upgaze_of_childhood_with_ataxia": 6,
    "DAGLA-related_disorder|not_provided": 2,
    "Benign_paroxysmal_tonic_upgaze_of_childhood_with_ataxia|See_cases": 1,
    "MYRF-related_disorder": 48,
    "Cardiac-urogenital_syndrome": 23,
    "Heart|_malformation_of|Congenital_diaphragmatic_hernia|Abnormality_of_the_genitourinary_system": 3,
    "Encephalitis/encephalopathy|_mild|_with_reversible_myelin_vacuolization|Cardiac-urogenital_syndrome": 4,
    "Encephalitis/encephalopathy|_mild|_with_reversible_myelin_vacuolization": 3,
    "MYRF-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Non-immune_hydrops_fetalis|Cardiac-urogenital_syndrome": 1,
    "not_provided|Cardiac-urogenital_syndrome": 2,
    "not_provided|MYRF-related_disorder": 4,
    "MYRF-related_disorder|not_provided": 2,
    "Scimitar_syndrome": 1,
    "Heart|_malformation_of|Abnormality_of_the_genitourinary_system": 2,
    "Inborn_genetic_diseases|Cardiac-urogenital_syndrome|Encephalitis/encephalopathy|_mild|_with_reversible_myelin_vacuolization": 1,
    "not_provided|not_specified|MYRF-related_disorder": 1,
    "Cardiac-urogenital_syndrome|Heart|_malformation_of|Congenital_diaphragmatic_hernia|Abnormality_of_the_genitourinary_system": 2,
    "Cardiac-urogenital_syndrome|Encephalitis/encephalopathy|_mild|_with_reversible_myelin_vacuolization": 4,
    "Dextrocardia|Heart|_malformation_of|Abnormality_of_the_genitourinary_system": 1,
    "MYRF-related_disorder|Heart|_malformation_of|Congenital_diaphragmatic_hernia|Abnormality_of_the_genitourinary_system": 1,
    "not_provided|Inborn_genetic_diseases|Scimitar_syndrome": 1,
    "not_specified|Cardiac-urogenital_syndrome": 1,
    "Inborn_genetic_diseases|MYRF-related_disorder": 1,
    "Cardiac-urogenital_syndrome|Disorder_of_sexual_differentiation": 1,
    "MYRF-related_disorder|Encephalitis/encephalopathy|_mild|_with_reversible_myelin_vacuolization|Cardiac-urogenital_syndrome": 1,
    "Cardiac-urogenital_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Cardiac-urogenital_syndrome|Encephalitis/encephalopathy|_mild|_with_reversible_myelin_vacuolization|MYRF-related_disorder": 1,
    "Cardiac-urogenital_syndrome|MYRF-related_disorder": 1,
    "Nanophthalmos_1": 2,
    "Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_Pigmentosa|_Recessive|Vitelliform_macular_dystrophy_2": 4,
    "Retinitis_Pigmentosa|_Recessive|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "not_provided|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_Pigmentosa|_Recessive|Vitelliform_macular_dystrophy_2": 2,
    "Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa": 1,
    "Autosomal_recessive_bestrophinopathy|Retinal_dystrophy": 2,
    "Vitelliform_macular_dystrophy_2|Retinal_dystrophy|not_provided": 2,
    "not_provided|Retinal_dystrophy|Vitelliform_macular_dystrophy_2": 3,
    "not_provided|BEST1-related_dominant_retinopathy": 2,
    "Retinal_dystrophy|not_provided|Vitelliform_macular_dystrophy_2": 10,
    "Vitelliform_macular_dystrophy_2|Retinal_dystrophy": 4,
    "Macular_dystrophy|Retinal_dystrophy|not_provided|Vitelliform_macular_dystrophy_2": 3,
    "Autosomal_recessive_bestrophinopathy|BEST1-related_dominant_retinopathy|Retinal_dystrophy|not_provided": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|not_provided|Retinal_dystrophy": 1,
    "Autosomal_recessive_bestrophinopathy|not_provided": 4,
    "Retinal_dystrophy|not_provided|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy": 1,
    "not_provided|Retinal_dystrophy|Autosomal_recessive_bestrophinopathy|BEST1-related_disorder": 1,
    "Autosomal_recessive_bestrophinopathy": 15,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_bestrophinopathy|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa_50|Vitelliform_macular_dystrophy_2": 1,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_bestrophinopathy": 3,
    "Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|Retinal_dystrophy|not_provided": 1,
    "not_provided|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa": 4,
    "BEST1-related_disorder": 10,
    "not_provided|BEST1-related_disorder": 2,
    "not_provided|Vitelliform_macular_dystrophy_2|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Retinal_dystrophy|not_specified|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|not_provided|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "BEST1-related_disorder|not_provided": 8,
    "Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "not_provided|Vitelliform_macular_dystrophy_2|BEST1-related_disorder|Autosomal_dominant_vitreoretinochoroidopathy|Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Vitelliform_macular_dystrophy_2|not_provided": 2,
    "Retinal_dystrophy|not_provided|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|not_provided|Retinal_dystrophy": 1,
    "Macular_dystrophy|Retinal_dystrophy|Vitelliform_macular_dystrophy_2|not_provided": 1,
    "not_provided|Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2": 1,
    "Retinal_dystrophy|Vitelliform_macular_dystrophy_2": 2,
    "Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy": 5,
    "not_provided|Autosomal_dominant_vitreoretinochoroidopathy|Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa_50": 1,
    "Autosomal_recessive_bestrophinopathy|not_provided|BEST1-related_disorder": 1,
    "not_provided|Autosomal_recessive_bestrophinopathy|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_50": 1,
    "Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy": 1,
    "BEST1-related_disorder|BEST1-related_dominant_retinopathy|Retinal_dystrophy|not_provided|Stargardt_disease|Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2": 1,
    "Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2": 1,
    "not_provided|Retinal_dystrophy|Autosomal_recessive_bestrophinopathy": 1,
    "Retinitis_pigmentosa|not_provided|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa_50": 1,
    "Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|Autosomal_dominant_vitreoretinochoroidopathy": 2,
    "Retinal_dystrophy|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|not_provided": 1,
    "BEST1-related_disorder|Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_50|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|Autosomal_dominant_vitreoretinochoroidopathy|Retinal_dystrophy|not_provided": 1,
    "BEST1-related_disorder|Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_50": 2,
    "Retinitis_pigmentosa_50|Autosomal_recessive_bestrophinopathy|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Autosomal_recessive_bestrophinopathy|Retinitis_pigmentosa_50|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "BEST1-related_disorder|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa_50|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|not_provided": 1,
    "Retinitis_pigmentosa_50|Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinal_dystrophy|not_provided": 1,
    "Autosomal_recessive_bestrophinopathy|Retinal_dystrophy|not_provided": 2,
    "not_provided|Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa_50": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_50": 1,
    "not_provided|Autosomal_dominant_vitreoretinochoroidopathy": 2,
    "Autosomal_dominant_vitreoretinochoroidopathy": 2,
    "not_provided|Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 2,
    "Vitelliform_macular_dystrophy_2|Retinal_dystrophy|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|not_provided": 2,
    "Microcornea|_rod-cone_dystrophy|_cataract|_and_posterior_staphyloma_2|not_provided": 1,
    "Vitelliform_macular_dystrophy_1|Retinal_dystrophy|not_provided|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2": 1,
    "Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa_50|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|not_provided|not_specified": 1,
    "BEST1-related_disorder|not_provided|Stargardt_disease|Vitelliform_macular_dystrophy_2": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa_50|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_50|Autosomal_recessive_bestrophinopathy|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2": 1,
    "Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|not_provided": 1,
    "BEST1-related_disorder|Vitelliform_macular_dystrophy_2|not_provided": 1,
    "BEST1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Iron_Overload|Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "not_provided|BEST1-related_disorder|Retinal_dystrophy": 2,
    "Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|Autosomal_dominant_vitreoretinochoroidopathy|Retinal_dystrophy|BEST1-related_dominant_retinopathy|Retinitis_pigmentosa|not_provided": 1,
    "Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|Iron_Overload|Retinitis_Pigmentosa|_Recessive|not_provided": 3,
    "not_provided|Cone-rod_dystrophy_6": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|BEST1-related_dominant_retinopathy|Vitelliform_macular_dystrophy_2|not_provided|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|Retinal_dystrophy|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|Iron_Overload|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|BEST1-related_disorder|Iron_Overload|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|BEST1-related_disorder": 1,
    "BEST1-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_50|Vitelliform_macular_dystrophy_2|Autosomal_recessive_bestrophinopathy|Autosomal_dominant_vitreoretinochoroidopathy|Iron_Overload|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Severe_early-childhood-onset_retinal_dystrophy|not_provided": 1,
    "BEST1-related_disorder|Retinal_dystrophy|not_provided|Autosomal_recessive_bestrophinopathy|Vitelliform_macular_dystrophy_2": 1,
    "Retinitis_pigmentosa|not_provided|Vitelliform_macular_dystrophy_2|not_specified|Autosomal_dominant_vitreoretinochoroidopathy|Iron_Overload|Retinitis_Pigmentosa|_Recessive": 1,
    "BEST1-related_disorder|Iron_Overload|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|not_provided": 1,
    "Inborn_genetic_diseases|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_pigmentosa_50|Autosomal_recessive_bestrophinopathy|not_provided": 1,
    "Iron_Overload|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 2,
    "not_provided|Autosomal_recessive_bestrophinopathy": 1,
    "Iron_Overload|BEST1-related_disorder|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2": 1,
    "Iron_Overload|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa|Vitelliform_macular_dystrophy_2|Autosomal_dominant_vitreoretinochoroidopathy": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|Hemochromatosis_type_5|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_Pigmentosa|_Recessive": 1,
    "Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|not_provided|Vitelliform_macular_dystrophy_2|Hemochromatosis_type_5|Retinitis_Pigmentosa|_Recessive": 1,
    "Iron_Overload": 3,
    "Hemochromatosis_type_5|Autosomal_dominant_vitreoretinochoroidopathy|Vitelliform_macular_dystrophy_2|Retinitis_pigmentosa": 1,
    "Vitelliform_macular_dystrophy_2|Hemochromatosis_type_5|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Vitelliform_macular_dystrophy_2|Hemochromatosis_type_5|Retinitis_pigmentosa|Autosomal_dominant_vitreoretinochoroidopathy|not_provided": 1,
    "Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_Pigmentosa|_Recessive|Vitelliform_macular_dystrophy_2|Iron_Overload|not_provided|Hemochromatosis_type_5": 2,
    "Hemochromatosis_type_5": 10,
    "FTH1-related_disorder": 5,
    "not_provided|FTH1-related_disorder": 1,
    "Neurodegeneration_with_brain_iron_accumulation_9|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_9": 1,
    "FTH1-related_disorder|Autosomal_dominant_vitreoretinochoroidopathy|Retinitis_Pigmentosa|_Recessive|not_provided|Vitelliform_macular_dystrophy_2|Iron_Overload|Hemochromatosis_type_5": 1,
    "FTH1-related_disorder|not_provided": 1,
    "Hemochromatosis_type_5|FTH1-related_disorder": 1,
    "ASRGL1-related_disorder": 1,
    "not_provided|ASRGL1-related_disorder": 3,
    "ASRGL1-related_disorder|not_provided": 2,
    "not_provided|not_specified|ASRGL1-related_disorder": 1,
    "ASRGL1-related_disorder|not_specified|not_provided": 1,
    "AHNAK-related_disorder": 8,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_1": 2,
    "AHNAK-related_disorder|not_provided": 1,
    "ROM1-related_disorder|not_provided": 2,
    "not_specified|not_provided|Retinitis_pigmentosa_7": 1,
    "not_provided|Retinitis_pigmentosa_7|_digenic": 1,
    "ROM1-related_disorder|Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_7|_digenic|Retinitis_pigmentosa_7": 1,
    "Retinitis_pigmentosa_7|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|ROM1-related_disorder|not_specified": 1,
    "Macular_dystrophy|Retinal_dystrophy|not_provided": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_7|not_specified": 1,
    "Retinitis_Pigmentosa|_Dominant|not_specified|not_provided": 1,
    "Larsen-like_syndrome|_B3GAT3_type": 162,
    "Larsen-like_syndrome|_B3GAT3_type|Inborn_genetic_diseases": 5,
    "Larsen-like_syndrome|_B3GAT3_type|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Larsen-like_syndrome|_B3GAT3_type": 3,
    "not_provided|Larsen-like_syndrome|_B3GAT3_type|Inborn_genetic_diseases": 2,
    "Larsen-like_syndrome|_B3GAT3_type|not_provided": 17,
    "not_provided|Larsen-like_syndrome|_B3GAT3_type": 13,
    "Larsen-like_syndrome|_B3GAT3_type|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Larsen-like_syndrome|_B3GAT3_type": 6,
    "Larsen-like_syndrome|_B3GAT3_type|MULTIPLE_JOINT_DISLOCATIONS|_SHORT_STATURE|_AND_CRANIOFACIAL_DYSMORPHISM_WITH_CONGENITAL_HEART_DEFECTS|Multiple_joint_dislocations|_short_stature|_craniofacial_dysmorphism|_with_or_without_congenital_heart_defects|not_provided": 1,
    "not_provided|Larsen-like_syndrome|_B3GAT3_type|not_specified": 1,
    "MULTIPLE_JOINT_DISLOCATIONS|_SHORT_STATURE|_AND_CRANIOFACIAL_DYSMORPHISM_WITHOUT_CONGENITAL_HEART_DEFECTS|Larsen-like_syndrome|_B3GAT3_type|not_provided": 1,
    "MULTIPLE_JOINT_DISLOCATIONS|_SHORT_STATURE|_AND_CRANIOFACIAL_DYSMORPHISM_WITH_CONGENITAL_HEART_DEFECTS": 1,
    "Inborn_genetic_diseases|B3GAT3-related_disorder|Larsen-like_syndrome|_B3GAT3_type": 1,
    "Larsen-like_syndrome|_B3GAT3_type|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "MULTIPLE_JOINT_DISLOCATIONS|_SHORT_STATURE|_AND_CRANIOFACIAL_DYSMORPHISM_WITHOUT_CONGENITAL_HEART_DEFECTS|Larsen-like_syndrome|_B3GAT3_type": 1,
    "Larsen-like_syndrome|_B3GAT3_type|B3GAT3-related_disorder": 1,
    "MULTIPLE_JOINT_DISLOCATIONS|_SHORT_STATURE|_AND_CRANIOFACIAL_DYSMORPHISM_WITHOUT_CONGENITAL_HEART_DEFECTS": 1,
    "not_provided|Inborn_genetic_diseases|Larsen-like_syndrome|_B3GAT3_type": 1,
    "Larsen-like_syndrome|_B3GAT3_type|B3GAT3-related_disorder|not_provided": 1,
    "B3GAT3-related_disorder": 1,
    "B3GAT3-related_disorder|Larsen-like_syndrome|_B3GAT3_type": 1,
    "B3GAT3-related_disorder|not_provided|Larsen-like_syndrome|_B3GAT3_type": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_provided": 16,
    "GANAB-related_disorder": 15,
    "not_provided|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 17,
    "GANAB-related_disorder|not_provided": 5,
    "POLYCYSTIC_KIDNEY_DISEASE_3_WITH_POLYCYSTIC_LIVER_DISEASE": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 102,
    "not_provided|POLYCYSTIC_KIDNEY_DISEASE_3_WITH_POLYCYSTIC_LIVER_DISEASE": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Autosomal_dominant_polycystic_liver_disease|Biliary_tract_abnormality": 1,
    "not_provided|GANAB-related_disorder": 6,
    "not_provided|GANAB-related_disorder|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Biliary_tract_abnormality": 1,
    "Congenital_myopathy_22B|_severe_fetal": 6,
    "POLYCYSTIC_KIDNEY_DISEASE_3_WITH_POLYCYSTIC_LIVER_DISEASE|not_provided|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 1,
    "Biliary_tract_abnormality|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Autosomal_dominant_polycystic_liver_disease|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 4,
    "GANAB-related_disorder|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|GANAB-related_disorder|Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_specified": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Inborn_genetic_diseases": 2,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|GANAB-related_disorder": 2,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 5,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 1,
    "not_provided|Renal_cyst": 2,
    "not_provided|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided|GANAB-related_disorder": 1,
    "not_provided|GANAB-related_disorder|Autosomal_dominant_polycystic_liver_disease": 1,
    "POLYCYSTIC_KIDNEY_DISEASE_3_WITH_POLYCYSTIC_LIVER_DISEASE|not_provided": 1,
    "POLYCYSTIC_KIDNEY_DISEASE_3_WITHOUT_POLYCYSTIC_LIVER_DISEASE": 1,
    "GANAB-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 6,
    "Chronic_kidney_disease|not_provided|Autosomal_dominant_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_provided|Inborn_genetic_diseases|GANAB-related_disorder": 1,
    "not_provided|GANAB-related_disorder|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 1,
    "not_provided|Inborn_genetic_diseases|GANAB-related_disorder": 2,
    "GANAB-related_disorder|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|GANAB-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_polycystic_liver_disease|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|POLYCYSTIC_KIDNEY_DISEASE_3_WITH_POLYCYSTIC_LIVER_DISEASE|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|GANAB-related_disorder": 1,
    "GANAB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_9": 1,
    "not_provided|UQCC3-related_disorder|not_specified": 1,
    "not_provided|not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_9": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 3,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2": 5,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2": 3,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|not_provided": 1,
    "Inborn_genetic_diseases|Monogenic_diabetes|Charcot-Marie-Tooth_disease_type_2|not_provided|Hereditary_spastic_paraplegia|Congenital_generalized_lipodystrophy_type_2": 1,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_specified|not_provided|BSCL2-related_Developmental_and_epileptic_encephalopathy|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17": 18,
    "Charcot-Marie-Tooth_disease_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|not_provided": 1,
    "PPARG-related_familial_partial_lipodystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy": 1,
    "Congenital_generalized_lipodystrophy_type_2|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Monogenic_diabetes|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|not_provided|Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Monogenic_diabetes|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Hereditary_spastic_paraplegia|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy": 3,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 3,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2": 1,
    "not_provided|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_type_2|not_specified|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy": 2,
    "BSCL2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Monogenic_diabetes": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Neuronopathy|_distal_hereditary_motor|_type_5A|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "BSCL2-related_disorder|not_provided": 2,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_2|Lipodystrophy|Neutrophilia_in_presence_of_infection|Isolated_systolic_hypertension|Triangular_shaped_proximal_phalanx_of_the_thumb|Hereditary_spastic_paraplegia|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_type_2": 5,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Severe_neurodegenerative_syndrome_with_lipodystrophy": 1,
    "Neurologic_Disorders/Seipinopathy|Inborn_genetic_diseases|Congenital_generalized_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy": 2,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "BSCL2-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|not_provided|Inborn_genetic_diseases|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Monogenic_diabetes|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "BSCL2-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|Inborn_genetic_diseases": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Congenital_generalized_lipodystrophy_type_2": 9,
    "Congenital_generalized_lipodystrophy_type_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|BSCL2-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases": 8,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|BSCL2-related_disorder|Berardinelli-Seip_congenital_lipodystrophy|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Lipodystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_generalized_lipodystrophy_type_2": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C": 3,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia|BSCL2-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17": 1,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2": 2,
    "Berardinelli-Seip_congenital_lipodystrophy": 7,
    "Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Inborn_genetic_diseases": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Berardinelli-Seip_congenital_lipodystrophy": 1,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia|Berardinelli-Seip_congenital_lipodystrophy": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2|BSCL2-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Lipodystrophy": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|BSCL2-related_disorder|not_provided|Monogenic_diabetes": 1,
    "not_specified|Hereditary_spastic_paraplegia|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|not_specified|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|BSCL2-related_disorder": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Lipodystrophy": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "not_provided|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy": 1,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17": 1,
    "not_specified|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Monogenic_diabetes": 1,
    "BSCL2-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_spastic_paraplegia_17": 1,
    "Charcot-Marie-Tooth_disease_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C": 2,
    "not_provided|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Berardinelli-Seip_congenital_lipodystrophy|Inborn_genetic_diseases|Congenital_generalized_lipodystrophy_type_2": 1,
    "Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5A|Inborn_genetic_diseases|not_provided": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Severe_neurodegenerative_syndrome_with_lipodystrophy": 1,
    "not_provided|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Congenital_generalized_lipodystrophy_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|not_specified|Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Abnormal_central_motor_function|Berardinelli-Seip_congenital_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|not_provided|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2|BSCL2-related_disorder|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Charcot-Marie-Tooth_disease_type_2|Berardinelli-Seip_congenital_lipodystrophy|Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2": 1,
    "Hereditary_spastic_paraplegia_17|Neuronopathy|_distal_hereditary_motor|_type_5C|Berardinelli-Seip_congenital_lipodystrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Hereditary_spastic_paraplegia|Neuronopathy|_distal_hereditary_motor|_type_5A|Peripheral_neuropathy": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Inborn_genetic_diseases|not_provided|Lipodystrophy": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Severe_neurodegenerative_syndrome_with_lipodystrophy|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Berardinelli-Seip_congenital_lipodystrophy|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Hereditary_spastic_paraplegia": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_specified|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Charcot-Marie-Tooth_disease_type_2": 2,
    "Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Inborn_genetic_diseases|not_provided|BSCL2-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|See_cases": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Hereditary_spastic_paraplegia_17|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Young-onset_Parkinson_disease": 1,
    "Monogenic_diabetes|Charcot-Marie-Tooth_disease_type_2|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|BSCL2-related_disorder|Congenital_generalized_lipodystrophy_type_2": 1,
    "Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A|Hereditary_spastic_paraplegia_17|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Congenital_generalized_lipodystrophy_type_2|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|not_specified": 1,
    "not_provided|Congenital_generalized_lipodystrophy_type_2|Neuronopathy|_distal_hereditary_motor|_type_5A": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_5A|not_provided|Hereditary_spastic_paraplegia|Congenital_generalized_lipodystrophy_type_2": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_5A|Hereditary_spastic_paraplegia|Congenital_generalized_lipodystrophy_type_2": 1,
    "not_provided|Hereditary_spastic_paraplegia_17|Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C": 1,
    "not_provided|Congenital_generalized_lipodystrophy_type_2|Hereditary_spastic_paraplegia_17|not_specified": 1,
    "Congenital_generalized_lipodystrophy_type_2|Severe_neurodegenerative_syndrome_with_lipodystrophy|Neuronopathy|_distal_hereditary_motor|_type_5C|Hereditary_spastic_paraplegia_17": 1,
    "Breast_carcinoma|Reduced_delayed_hypersensitivity|Symphalangism_affecting_the_proximal_phalanx_of_the_4th_finger": 1,
    "HNRNPUL2-related_disorder": 9,
    "not_specified|HNRNPUL2-related_disorder": 1,
    "Neurodevelopmental_disorder_with_seizures_and_brain_abnormalities": 1,
    "SLC3A2-related_disorder": 1,
    "See_cases|CHRM1-related_neurodevelopmental_disorder": 1,
    "SLC22A25-related_disorder": 9,
    "not_specified|SLC22A25-related_disorder": 1,
    "Lipodystrophy|_familial_partial|_type_9": 3,
    "ATL3-related_disorder": 2,
    "Neuropathy|_hereditary_sensory|_type_1F": 350,
    "Neuropathy|_hereditary_sensory|_type_1F|Inborn_genetic_diseases": 30,
    "Neuropathy|_hereditary_sensory|_type_1F|not_provided": 17,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_1F": 22,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory|_type_1F|ATL3-related_disorder": 1,
    "not_provided|Neuropathy|_hereditary_sensory|_type_1F|Inborn_genetic_diseases": 3,
    "ATL3-related_disorder|Neuropathy|_hereditary_sensory|_type_1F|Inborn_genetic_diseases": 1,
    "not_specified|Neuropathy|_hereditary_sensory|_type_1F": 1,
    "Neuropathy|_hereditary_sensory|_type_1F|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_1F|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Neuropathy|_hereditary_sensory|_type_1F": 11,
    "Neuropathy|_hereditary_sensory|_type_1F|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Neuropathy|_hereditary_sensory|_type_1F|not_provided|Inborn_genetic_diseases": 3,
    "Neuropathy|_hereditary_sensory|_type_1F|Inborn_genetic_diseases|not_provided": 1,
    "ATL3-related_disorder|Neuropathy|_hereditary_sensory|_type_1F": 1,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory|_type_1F": 1,
    "Neuropathy|_hereditary_sensory|_type_1F|ATL3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory|_type_1F": 1,
    "INTELLECTUAL_DEVELOPMENTAL_DISORDER|_AUTOSOMAL_DOMINANT_76|Autism_spectrum_disorder": 2,
    "Autism_spectrum_disorder|INTELLECTUAL_DEVELOPMENTAL_DISORDER|_AUTOSOMAL_DOMINANT_76": 3,
    "Autism|INTELLECTUAL_DEVELOPMENTAL_DISORDER|_AUTOSOMAL_DOMINANT_76": 1,
    "MARK2-associated_disorder": 1,
    "INTELLECTUAL_DEVELOPMENTAL_DISORDER|_AUTOSOMAL_DOMINANT_76|not_provided|Autism_spectrum_disorder": 1,
    "Compulsive_behaviors|Anxiety|Dyslexia|Attention_deficit_hyperactivity_disorder|Delayed_speech_and_language_development|Seizure": 1,
    "MARK2-associated_neurodevelopmental_disorder|Autism_spectrum_disorder": 1,
    "Autism_spectrum_disorder|Intellectual_disability": 1,
    "COX8A-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_15|not_provided": 2,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_15": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_15|COX8A-related_disorder": 1,
    "not_specified|Peripheral_neuropathy": 16,
    "FLRT1-related_disorder|not_provided|Peripheral_neuropathy": 1,
    "Peripheral_neuropathy|FLRT1-related_disorder|not_provided": 1,
    "FLRT1-related_disorder|Peripheral_neuropathy|not_provided": 1,
    "Peripheral_neuropathy|not_specified": 8,
    "Peripheral_neuropathy|not_provided": 11,
    "FLRT1-related_disorder|Peripheral_neuropathy": 4,
    "FLRT1-related_disorder": 2,
    "not_specified|FLRT1-related_disorder": 1,
    "not_provided|not_specified|Peripheral_neuropathy": 1,
    "not_provided|Peripheral_neuropathy|FLRT1-related_disorder": 1,
    "Leukocyte_adhesion_deficiency_3": 425,
    "Leukocyte_adhesion_deficiency_3|not_specified": 3,
    "FERMT3-related_disorder": 2,
    "Leukocyte_adhesion_deficiency_3|Inborn_genetic_diseases": 22,
    "Leukocyte_adhesion_deficiency|Leukocyte_adhesion_deficiency_3": 1,
    "not_specified|not_provided|Leukocyte_adhesion_deficiency_3": 4,
    "not_provided|Leukocyte_adhesion_deficiency_3|not_specified|FERMT3-related_disorder": 1,
    "not_provided|not_specified|Leukocyte_adhesion_deficiency_3": 1,
    "Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_3": 14,
    "Leukocyte_adhesion_deficiency_3|FERMT3-related_disorder": 2,
    "FERMT3-related_disorder|Leukocyte_adhesion_deficiency_3|not_provided": 1,
    "Leukocyte_adhesion_deficiency_3|not_provided": 11,
    "FERMT3-related_disorder|Leukocyte_adhesion_deficiency_3|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Leukocyte_adhesion_deficiency_3": 3,
    "Leukocyte_adhesion_deficiency|Leukocyte_adhesion_deficiency_3|not_provided": 1,
    "not_provided|Leukocyte_adhesion_deficiency_3": 8,
    "not_specified|Leukocyte_adhesion_deficiency_3|not_provided": 3,
    "Leukocyte_adhesion_deficiency_3|Inborn_genetic_diseases|not_specified|not_provided|FERMT3-related_disorder": 1,
    "FERMT3-related_disorder|Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_3|not_provided": 1,
    "Leukocyte_adhesion_deficiency_3|Inborn_genetic_diseases|FERMT3-related_disorder": 1,
    "Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_3|not_provided": 1,
    "not_provided|Leukocyte_adhesion_deficiency_3|Inborn_genetic_diseases|FERMT3-related_disorder": 1,
    "FERMT3-related_disorder|not_provided|Leukocyte_adhesion_deficiency_3": 1,
    "not_provided|FERMT3-related_disorder|Leukocyte_adhesion_deficiency_3": 1,
    "not_specified|Leukocyte_adhesion_deficiency_3|Inborn_genetic_diseases": 1,
    "FERMT3-related_disorder|Leukocyte_adhesion_deficiency_3": 3,
    "not_provided|Leukocyte_adhesion_deficiency_3|not_specified": 1,
    "Leukocyte_adhesion_deficiency_3|FERMT3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Leukocyte_adhesion_deficiency_3|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_3": 1,
    "not_provided|PLCB3-related_disorder": 1,
    "Spondylometaphyseal_dysplasia_with_corneal_dystrophy": 1,
    "not_specified|Spondylometaphyseal_dysplasia_with_corneal_dystrophy": 1,
    "KCNK4-related_disorder|not_provided": 4,
    "KCNK4-related_disorder": 2,
    "not_specified|KCNK4-related_disorder|not_provided": 1,
    "Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome": 9,
    "not_provided|KCNK4-related_disorder": 5,
    "not_provided|Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome": 2,
    "not_specified|Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome|not_provided": 1,
    "Abnormal_facial_shape|Intellectual_disability|Seizure|Generalized_hypertrichosis|Gingival_overgrowth|Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome": 1,
    "Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome|not_specified": 1,
    "Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome|Benign_Rolandic_epilepsy|not_provided": 1,
    "Abnormal_facial_shape|Generalized_hypertrichosis|Intellectual_disability|Gingival_overgrowth|Seizure|Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome": 1,
    "Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome|not_provided": 1,
    "KCNK4-related_disorder|Facial_dysmorphism|_hypertrichosis|_epilepsy|_intellectual/developmental_delay|_and_gingival_overgrowth_syndrome|not_provided": 1,
    "SLC22A11-related_disorder": 3,
    "SLC22A11-related_disorder|not_provided": 1,
    "Dalmatian_hypouricemia": 101,
    "Dalmatian_hypouricemia|not_provided": 26,
    "SLC22A12-related_disorder": 2,
    "Inborn_genetic_diseases|Dalmatian_hypouricemia|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Dalmatian_hypouricemia": 4,
    "Familial_renal_hypouricemia": 1,
    "not_specified|Dalmatian_hypouricemia|not_provided": 4,
    "Familial_renal_hypouricemia|Dalmatian_hypouricemia|not_provided": 1,
    "Inborn_genetic_diseases|Dalmatian_hypouricemia": 3,
    "not_provided|not_specified|Dalmatian_hypouricemia": 1,
    "not_provided|Dalmatian_hypouricemia|Inborn_genetic_diseases": 1,
    "SLC22A12-related_disorder|Dalmatian_hypouricemia|not_provided": 1,
    "Dalmatian_hypouricemia|SLC22A12-related_disorder|not_provided": 2,
    "not_provided|Dalmatian_hypouricemia|SLC22A12-related_disorder|Familial_renal_hypouricemia": 1,
    "SLC22A12-related_disorder|not_provided|Dalmatian_hypouricemia": 2,
    "Dalmatian_hypouricemia|Inborn_genetic_diseases|not_provided": 3,
    "SLC22A12-related_disorder|not_provided": 1,
    "Dalmatian_hypouricemia|Inborn_genetic_diseases": 2,
    "Dalmatian_hypouricemia|not_provided|Inborn_genetic_diseases": 1,
    "Schizophrenia|Autism_spectrum_disorder": 1,
    "NRXN2-related_disorder": 11,
    "not_specified|NRXN2-related_autism_spectrum_disorder": 1,
    "NRXN2-related_disorder|not_specified": 1,
    "not_specified|NRXN2-related_disorder": 3,
    "NRXN2-related_Austism_Spectrum_Disorder|not_specified": 1,
    "not_provided|not_specified|NRXN2-related_disorder": 2,
    "NRXN2-associated_Neurodevelopmental_disorder": 1,
    "not_specified|not_provided|NRXN2-related_disorder": 3,
    "not_provided|NRXN2-related_disorder": 2,
    "See_cases|NRXN2-related_disorder": 1,
    "NRXN2-related_disorder|not_provided": 2,
    "Severe_intellectual_deficiency|Epilepsy": 2,
    "not_provided|NRXN2-related_disorder|not_specified": 1,
    "RASGRP2-related_disorder|not_provided": 3,
    "Platelet-type_bleeding_disorder_18": 12,
    "not_provided|Platelet-type_bleeding_disorder_18": 6,
    "Platelet-type_bleeding_disorder_18|RASGRP2-related_disorder|not_provided|Abnormal_platelet_aggregation": 1,
    "not_provided|RASGRP2-related_disorder|not_specified": 2,
    "RASGRP2-related_disorder": 1,
    "Abnormal_platelet_aggregation": 10,
    "Platelet-type_bleeding_disorder_18|Abnormal_bleeding|Abnormal_platelet_aggregation": 1,
    "not_provided|RASGRP2-related_disorder": 2,
    "Inborn_genetic_diseases|Thrombocytopenia|Abnormal_bleeding": 1,
    "Glycogen_storage_disease|_type_V": 1171,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_V": 18,
    "not_specified|not_provided|Glycogen_storage_disease|_type_V": 13,
    "Inborn_genetic_diseases|Tip-toe_gait|not_provided|Glycogen_storage_disease|_type_V": 1,
    "Glycogen_storage_disease|_type_V|not_specified": 16,
    "Glycogen_storage_disease|_type_V|Inborn_genetic_diseases": 16,
    "not_provided|Glycogen_storage_disease|_type_V": 51,
    "Glycogen_storage_disease|_type_V|not_provided": 44,
    "not_specified|Glycogen_storage_disease|_type_V|not_provided": 2,
    "Glycogen_storage_disease|_type_V|PYGM-related_disorder": 8,
    "PYGM-related_disorder|Glycogen_storage_disease|_type_V": 2,
    "not_provided|Glycogen_storage_disease|_type_V|not_specified": 4,
    "not_specified|Glycogen_storage_disease|_type_V": 16,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_V|not_specified|not_provided": 2,
    "PYGM-related_disorder|Glycogen_storage_disease|_type_V|not_provided": 2,
    "Glycogen_storage_disease|_type_V|Rhabdomyolysis|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Glycogen_storage_disease|_type_V": 3,
    "not_provided|Glycogen_storage_disease|_type_V|PYGM-related_disorder": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_V|not_provided": 3,
    "Glycogen_storage_disease|Glycogen_storage_disease|_type_V": 1,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease|_type_V": 5,
    "PYGM-related_disorder|not_provided|Glycogen_storage_disease|_type_V|Tip-toe_gait": 2,
    "Elevated_circulating_creatine_kinase_concentration|Glycogen_storage_disease|_type_V": 1,
    "PYGM-related_disorder|not_specified|not_provided|Glycogen_storage_disease|_type_V": 1,
    "not_provided|Glycogen_storage_disease|_type_V|Tip-toe_gait": 2,
    "Glycogen_storage_disease|_type_V|See_cases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Glycogen_storage_disease|_type_V": 2,
    "Glycogen_storage_disease|_type_V|Inborn_genetic_diseases|not_provided": 2,
    "Glycogen_storage_disease|_type_V|not_provided|not_specified": 2,
    "Glycogen_storage_disease|_type_V|Tip-toe_gait": 5,
    "See_cases|Glycogen_storage_disease|_type_V": 1,
    "Glycogen_storage_disease|_type_V|Tip-toe_gait|not_specified": 1,
    "Glycogen_storage_disease|PYGM-related_disorder|not_provided|not_specified|Glycogen_storage_disease|_type_V": 1,
    "not_provided|PYGM-related_disorder|Glycogen_storage_disease|_type_V": 2,
    "PYGM-related_disorder|not_specified|not_provided|Glycogen_storage_disease|_type_V|Tip-toe_gait": 2,
    "PYGM-related_disorder|not_specified|Glycogen_storage_disease|_type_V": 1,
    "Glycogen_storage_disease|_type_V|not_specified|PYGM-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease|_type_V": 3,
    "Glycogen_storage_disease|_type_V|not_specified|not_provided": 3,
    "Tip-toe_gait|Glycogen_storage_disease|_type_V": 1,
    "Glycogen_storage_disease|_type_V|not_specified|Tip-toe_gait": 1,
    "Glycogen_storage_disease|_type_V|PYGM-related_disorder|not_provided": 1,
    "Glycogen_storage_disease|_type_V|Tip-toe_gait|not_provided": 1,
    "not_provided|not_specified|Glycogen_storage_disease|_type_V|PYGM-related_disorder": 1,
    "not_provided|PYGM-related_disorder|not_specified|Glycogen_storage_disease|_type_V": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_V|not_provided|Elevated_circulating_creatine_kinase_concentration": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Glycogen_storage_disease|_type_V": 1,
    "PYGM-related_disorder|not_provided|Glycogen_storage_disease|_type_V": 1,
    "Glycogen_storage_disease|_type_V|Myopathy": 1,
    "Glycogen_storage_disease|_type_V|McArdle_disease|_mild": 1,
    "PYGM-related_disorder": 1,
    "PYGM-related_disorder|not_provided|not_specified|Glycogen_storage_disease|_type_V": 1,
    "Glycogen_storage_disease|_type_V|not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "not_provided|Glycogen_storage_disease|_type_V|McArdle_disease|_mild": 1,
    "PYGM-related_disorder|not_provided|Glycogen_storage_disease|_type_V|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Glycogen_storage_disease|_type_V|Tip-toe_gait|High_myopia": 1,
    "Hereditary_skeletal_muscle_disorder|Inborn_genetic_diseases|not_provided|Tip-toe_gait|Glycogen_storage_disease|_type_V|See_cases": 1,
    "SF1-related_neurodevelopmental_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism": 11,
    "Multiple_endocrine_neoplasia|Hyperparathyroidism": 7,
    "Multiple_endocrine_neoplasia|Hyperparathyroidism|not_provided": 1,
    "Somatotroph_adenoma|not_specified|Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism": 1,
    "Multiple_endocrine_neoplasia|_type_1|Somatotroph_adenoma": 1,
    "MEN1-related_disorder": 6,
    "Hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1": 6,
    "Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism|not_provided": 2,
    "Hyperparathyroidism|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_1": 33,
    "Multiple_endocrine_neoplasia|_type_1|not_specified": 11,
    "Somatotroph_adenoma": 45,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 406,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 353,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_1": 7,
    "Hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|Multiple_endocrine_neoplasia": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 21,
    "Multiple_endocrine_neoplasia|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 19,
    "Multiple_endocrine_neoplasia|_type_1|not_provided": 28,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided": 26,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 21,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder": 8,
    "Multiple_endocrine_neoplasia|_type_1|not_provided|MEN1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1|not_specified": 2,
    "Adrenocortical_adenoma": 1,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 21,
    "Multiple_endocrine_neoplasia|_type_1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|not_provided|Primary_hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 6,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1": 43,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1|Lung_carcinoid_tumor": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism|not_provided|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 1,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 3,
    "Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_1|not_specified|Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome": 1,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|MEN1-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_specified": 2,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1": 2,
    "not_provided|MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_specified": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 3,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism_1": 1,
    "not_provided|Familial_isolated_hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1": 1,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_1": 1,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|Pituitary_adenoma_5|_multiple_types": 1,
    "MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "Angiofibroma|_somatic": 2,
    "MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1|not_provided": 1,
    "Multiple_endocrine_neoplasia|_type_1|not_specified|Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1": 1,
    "Gigantism|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism": 1,
    "Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Pituitary_dependent_hypercortisolism|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder|Diffuse_midline_glioma|_H3_K27-altered": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_1": 4,
    "Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder": 1,
    "not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "Multiple_endocrine_neoplasia|_type_1|not_specified|not_provided": 1,
    "Pituitary_adenoma_5|_multiple_types|Multiple_endocrine_neoplasia|_type_1": 1,
    "Multiple_endocrine_neoplasia|_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|not_provided": 1,
    "not_specified|Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided": 1,
    "Hyperparathyroidism|not_provided|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "MEN1-related_disorder|Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "MEN1-related_disorder|Hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Diabetes_mellitus|Hypertensive_disorder|Parathyroid_gland_adenoma|Chronic_diarrhea|Gastrointestinal_stromal_tumor|Thyroid_adenoma": 1,
    "Multiple_endocrine_neoplasia|_type_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism|not_provided|Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hyperparathyroidism|Multiple_endocrine_neoplasia|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|not_provided|not_specified|Hyperparathyroidism|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided|not_specified": 1,
    "Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder": 1,
    "Multiple_endocrine_neoplasia|_type_1|Parathyroid_gland_adenoma|Pancreatic_insulin-producing_neuroendocrine_tumor|Calcium_nephrolithiasis|Primary_hyperparathyroidism|Medullary_thyroid_carcinoma|Abnormal_circulating_calcium_concentration": 1,
    "not_provided|MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_provided|Multiple_endocrine_neoplasia|_type_1|Lipoma|_somatic|Hereditary_cancer-predisposing_syndrome": 1,
    "Multiple_endocrine_neoplasia|_type_1|not_provided|MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer": 1,
    "Primary_hyperparathyroidism": 1,
    "not_provided|Parathyroid_adenoma|_somatic|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_specified|Hyperparathyroidism|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1": 1,
    "Hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_1": 1,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Multiple_endocrine_neoplasia|_type_1": 1,
    "not_provided|not_specified|Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|MEN1-related_disorder|Multiple_endocrine_neoplasia|_type_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia|_type_1|MEN1-related_disorder": 1,
    "MEN1-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia|_type_1|not_provided|not_specified": 1,
    "MEN1-related_disorder|Multiple_endocrine_neoplasia|Hyperparathyroidism": 1,
    "Multiple_endocrine_neoplasia|_type_1|not_specified|Hyperparathyroidism|not_provided": 1,
    "not_specified|Multiple_endocrine_neoplasia|_type_1|Hyperparathyroidism|not_provided": 1,
    "PPP2R5B-related_disorder": 4,
    "not_provided|PPP2R5B-related_disorder": 2,
    "Microcornea|_rod-cone_dystrophy|_cataract|_and_posterior_staphyloma_1": 1,
    "ARL2-related_condition": 1,
    "Pontocerebellar_hypoplasia|_type_13|not_specified": 1,
    "Pontocerebellar_hypoplasia|_type_13": 7,
    "VPS51-related_disorder": 4,
    "VPS51-related_disorder|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia|_type_13": 1,
    "COMBINED_OXIDATIVE_PHOSPHORYLATION_DEFICIENCY_60|Perrault_syndrome_1": 2,
    "Perrault_syndrome_1|COMBINED_OXIDATIVE_PHOSPHORYLATION_DEFICIENCY_60": 1,
    "Combined_oxidative_phosphorylation_defect_type_2|Perrault_syndrome_1": 1,
    "not_specified|Seizure|Hypospadias|Tracheomalacia|Intellectual_disability|_moderate|Periventricular_leukomalacia|Hypotonia|Abnormal_facial_shape|Delayed_speech_and_language_development|Encephalomalacia": 1,
    "Periventricular_leukomalacia|Abnormal_facial_shape|Hypotonia|Seizure|Intellectual_disability|_moderate|Delayed_speech_and_language_development|Encephalomalacia|Hypospadias|Tracheomalacia": 1,
    "Autosomal_recessive_spastic_paraplegia_type_76": 21,
    "Autosomal_recessive_spastic_paraplegia_type_76|not_provided": 14,
    "not_provided|Autosomal_recessive_spastic_paraplegia_type_76": 4,
    "CAPN1-related_disorder": 3,
    "Autosomal_recessive_spastic_paraplegia_type_76|CAPN1-related_disorder|not_provided": 1,
    "Autosomal_recessive_spastic_paraplegia_type_76|not_specified": 1,
    "Autosomal_recessive_spastic_paraplegia_type_76|Hereditary_spastic_paraplegia_11|not_provided": 1,
    "not_provided|CAPN1-related_disorder": 1,
    "CAPN1-related_disorder|not_provided": 1,
    "Telomere_Biology_Disorder": 2,
    "not_specified|Telomere_Biology_Disorder": 1,
    "not_provided|DPF2-related_disorder": 6,
    "DPF2-related_disorder": 6,
    "DPF2-related_disorder|not_provided": 2,
    "Coffin-Siris_syndrome_7": 19,
    "not_provided|Coffin-Siris_syndrome_7": 2,
    "Coffin-Siris_syndrome_7|Inborn_genetic_diseases": 2,
    "Coffin-Siris_syndrome_7|Coffin-Siris_syndrome_1": 1,
    "Coffin-Siris_syndrome_7|not_provided": 2,
    "Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome": 21,
    "SCYL1-related_disorder": 6,
    "SCYL1-related_disorder|not_provided": 7,
    "not_provided|SCYL1-related_disorder": 4,
    "not_provided|Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome": 3,
    "Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome|SCYL1-related_disorder": 1,
    "Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Acute_infantile_liver_failure-cerebellar_ataxia-peripheral_sensory_motor_neuropathy_syndrome": 1,
    "not_provided|SCYL1-related_disorder|Inborn_genetic_diseases": 1,
    "SCYL1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "LTBP3-related_disorder": 12,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|not_provided": 12,
    "Geleophysic_dysplasia_3": 6,
    "not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome": 12,
    "Brachyolmia-amelogenesis_imperfecta_syndrome": 861,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases": 139,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder": 6,
    "Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome": 204,
    "not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases": 1,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder|Inborn_genetic_diseases": 2,
    "LTBP3-related_disorder|Brachyolmia-amelogenesis_imperfecta_syndrome": 7,
    "Inborn_genetic_diseases|not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome": 2,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder": 10,
    "Inborn_genetic_diseases|not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder": 1,
    "LTBP3-related_disorder|not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "LTBP3-related_disorder|Inborn_genetic_diseases|Geleophysic_dysplasia_3|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "LTBP3-related_disorder|Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome": 10,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Geleophysic_dysplasia_3": 5,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "Geleophysic_dysplasia_3|Brachyolmia-amelogenesis_imperfecta_syndrome": 4,
    "Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome|not_provided": 8,
    "not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|Brachyolmia-amelogenesis_imperfecta_syndrome": 2,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Geleophysic_dysplasia": 1,
    "Heritable_Thoracic_Aortic_Disease|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|not_provided|Inborn_genetic_diseases|LTBP3-related_disorder": 1,
    "Heritable_Thoracic_Aortic_Disease": 1,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Geleophysic_dysplasia_3|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|LTBP3-related_disorder|not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_specified|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|LTBP3-related_disorder|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_specified|Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases": 1,
    "LTBP3-related_disorder|Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases": 1,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases|not_provided|LTBP3-related_disorder": 1,
    "LTBP3-related_disorder|Inborn_genetic_diseases|not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "LTBP3-related_disorder|Geleophysic_dysplasia_3|Brachyolmia-amelogenesis_imperfecta_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "LTBP3-related_disorder|not_provided|Inborn_genetic_diseases|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_provided|Heritable_Thoracic_Aortic_Disease|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_specified|not_provided|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_specified|Geleophysic_dysplasia_3|Brachyolmia-amelogenesis_imperfecta_syndrome": 1,
    "not_specified|Geleophysic_dysplasia_3|Brachyolmia-amelogenesis_imperfecta_syndrome|LTBP3-related_disorder|not_provided": 1,
    "Brachyolmia-amelogenesis_imperfecta_syndrome|Geleophysic_dysplasia_3|not_provided": 1,
    "EHBP1L1-related_disorder": 2,
    "EHBP1L1-related_disorder|not_specified": 2,
    "not_provided|RELA-related_disorder": 7,
    "RELA-related_disorder": 2,
    "Mucocutaneous_ulceration|_chronic": 7,
    "RELA-related_disorder|not_provided": 3,
    "not_provided|Mucocutaneous_ulceration|_chronic": 3,
    "Mucocutaneous_ulceration|_chronic|not_provided|RELA-related_disorder": 2,
    "Mucocutaneous_ulceration": 1,
    "Mucocutaneous_ulceration|_chronic|not_provided": 4,
    "Mucocutaneous_ulceration|_chronic|not_specified|not_provided": 1,
    "RELA-related_disorder|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies|_sleep_disturbance|_and_brain_abnormalities": 17,
    "not_specified|KAT5-related_disorder": 1,
    "KAT5-related_disorder": 3,
    "not_specified|Neurodevelopmental_disorder_with_dysmorphic_facies|_sleep_disturbance|_and_brain_abnormalities": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies|_sleep_disturbance|_and_brain_abnormalities|not_specified": 1,
    "Aicardi-Goutieres_syndrome_3|not_provided": 15,
    "not_provided|Aicardi-Goutieres_syndrome_3": 10,
    "Aicardi-Goutieres_syndrome_3": 303,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_3|not_provided": 1,
    "Aicardi-Goutieres_syndrome_3|Inborn_genetic_diseases": 8,
    "RNASEH2C-related_disorder": 3,
    "not_specified|Aicardi-Goutieres_syndrome_3": 2,
    "RNASEH2C-related_disorder|Aicardi-Goutieres_syndrome_3": 2,
    "not_specified|RNASEH2C-related_disorder|not_provided|Aicardi-Goutieres_syndrome_3": 1,
    "Aicardi-Goutieres_syndrome_3|Aicardi_Goutieres_syndrome|not_provided": 1,
    "not_specified|not_provided|Aicardi-Goutieres_syndrome_3": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_3|not_provided": 2,
    "Aicardi-Goutieres_syndrome_3|RNASEH2C-related_disorder": 1,
    "Aicardi-Goutieres_syndrome_3|Aicardi_Goutieres_syndrome|Inborn_genetic_diseases": 1,
    "Aicardi-Goutieres_syndrome_3|Aicardi_Goutieres_syndrome|not_specified": 1,
    "not_provided|Aicardi-Goutieres_syndrome_3|RNASEH2C-related_disorder": 2,
    "Aicardi_Goutieres_syndrome|not_provided|Abnormality_of_the_nervous_system|Aicardi-Goutieres_syndrome_3": 1,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_3": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_3": 2,
    "Aicardi-Goutieres_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Aicardi-Goutieres_syndrome_3|not_specified": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia": 2,
    "Cutis_laxa|_autosomal_recessive|_type_1B|not_provided": 7,
    "Cutis_laxa|_autosomal_recessive|_type_1B|not_specified|not_provided": 2,
    "Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 48,
    "Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 4,
    "not_specified|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided": 1,
    "Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B": 54,
    "Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "not_provided|Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B": 6,
    "Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B|not_specified": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_recessive|_type_1B": 4,
    "Cardiovascular_phenotype|EFEMP2-related_disorder|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_specified|Cutis_laxa|_autosomal_recessive|_type_1B": 3,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 8,
    "Cutis_laxa|_autosomal_recessive|_type_1B|not_provided|Cardiovascular_phenotype": 4,
    "Cutis_laxa|_autosomal_recessive|_type_1B|not_specified|Cardiovascular_phenotype": 4,
    "not_specified|EFEMP2-related_disorder|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1B|Cutis_laxa|_autosomal_recessive|_type_1A": 3,
    "Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder": 1,
    "not_specified|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 2,
    "Cutis_laxa": 23,
    "Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 4,
    "not_specified|Cutis_laxa|_autosomal_recessive|_type_1B|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|EFEMP2-related_disorder|not_specified|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "not_provided|EFEMP2-related_disorder|not_specified|Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B": 2,
    "Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|EFEMP2-related_disorder|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 1,
    "not_specified|Cutis_laxa|_autosomal_recessive|_type_1B": 4,
    "not_provided|not_specified|Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|Cutis_laxa|_autosomal_recessive|_type_1A": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|EFEMP2-related_disorder|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1B|not_specified": 2,
    "Cutis_laxa|_autosomal_recessive|_type_1B|not_provided|Familial_aortopathy": 1,
    "not_specified|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided|Cardiovascular_phenotype": 1,
    "EFEMP2-related_disorder": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 2,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder|not_specified": 1,
    "not_provided|not_specified|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "not_specified|EFEMP2-related_disorder|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cutis_laxa|_autosomal_recessive|_type_1B|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|EFEMP2-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Cutis_laxa|_autosomal_recessive|_type_1B|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "EFEMP2-related_disorder|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 1,
    "EFEMP2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Cutis_laxa|_autosomal_recessive|_type_1B|Cardiovascular_phenotype": 1,
    "Tall_stature-intellectual_disability-renal_anomalies_syndrome|Inborn_genetic_diseases": 1,
    "Tall_stature-intellectual_disability-renal_anomalies_syndrome|not_provided": 1,
    "Tall_stature-intellectual_disability-renal_anomalies_syndrome": 8,
    "FIBP-related_disorder": 3,
    "FIBP-related_disorder|not_provided": 2,
    "Learning_disability|Macrocephaly|Overgrowth|Large_hands|Congenital_anomaly_of_face|Congenital_ocular_coloboma|Tall_stature-intellectual_disability-renal_anomalies_syndrome": 1,
    "Nestor-Guillermo_progeria_syndrome": 22,
    "Nestor-Guillermo_progeria_syndrome|not_provided": 5,
    "not_provided|Nestor-Guillermo_progeria_syndrome": 1,
    "CST6-related_disorder": 1,
    "Ectodermal_dysplasia_15|_hypohidrotic/hair_type": 3,
    "Spermatogenic_failure_7": 40,
    "not_specified|Spermatogenic_failure_7": 6,
    "Spermatogenic_failure_7|not_provided": 10,
    "Spermatogenic_failure_7|CATSPER1-related_disorder|not_provided": 3,
    "CATSPER1-related_disorder": 4,
    "Spermatogenic_failure_7|not_specified": 2,
    "not_provided|Spermatogenic_failure_7": 8,
    "CATSPER1-related_disorder|Spermatogenic_failure_7": 2,
    "not_provided|CATSPER1-related_disorder|Spermatogenic_failure_7": 1,
    "not_provided|Male_infertility": 1,
    "SF3B2-related_disorder": 3,
    "PACS1-related_disorder": 10,
    "Schuurs-Hoeijmakers_syndrome": 514,
    "not_specified|Inborn_genetic_diseases|PACS1-related_disorder": 1,
    "not_provided|PACS1-related_disorder|not_specified|Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome": 1,
    "not_provided|Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases": 5,
    "not_specified|not_provided|Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|PACS1-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome": 2,
    "not_provided|PACS1-related_disorder|Schuurs-Hoeijmakers_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Schuurs-Hoeijmakers_syndrome": 3,
    "Schuurs-Hoeijmakers_syndrome|not_provided|Intellectual_disability|PACS1-related_disorder": 1,
    "Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases": 16,
    "Schuurs-Hoeijmakers_syndrome|not_provided": 26,
    "not_provided|Schuurs-Hoeijmakers_syndrome|not_specified": 1,
    "not_provided|Schuurs-Hoeijmakers_syndrome": 20,
    "Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome": 15,
    "not_specified|Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome|not_provided": 2,
    "Schuurs-Hoeijmakers_syndrome|not_provided|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome|not_provided": 5,
    "Global_developmental_delay|PACS1-related_disorder|Neurodevelopmental_disorder|Inborn_genetic_diseases|PACS1-related_syndrome|Intellectual_disability|not_provided|Schuurs-Hoeijmakers_syndrome|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome": 4,
    "Inborn_genetic_diseases|Intellectual_disability|Schuurs-Hoeijmakers_syndrome|not_specified|PACS1-related_disorder|not_provided": 1,
    "not_specified|Schuurs-Hoeijmakers_syndrome|PACS1-related_disorder": 1,
    "PACS1-related_disorder|Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Schuurs-Hoeijmakers_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|PACS1-related_disorder|Schuurs-Hoeijmakers_syndrome": 1,
    "Schuurs-Hoeijmakers_syndrome|not_specified": 4,
    "PACS1-related_disorder|Schuurs-Hoeijmakers_syndrome": 6,
    "not_specified|Schuurs-Hoeijmakers_syndrome": 7,
    "Schuurs-Hoeijmakers_syndrome|PACS1-related_disorder|not_specified|not_provided": 1,
    "Schuurs-Hoeijmakers_syndrome|Aganglionic_megacolon": 1,
    "not_provided|not_specified|Schuurs-Hoeijmakers_syndrome": 2,
    "Schuurs-Hoeijmakers_syndrome|not_specified|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|Schuurs-Hoeijmakers_syndrome": 1,
    "not_specified|Schuurs-Hoeijmakers_syndrome|not_provided": 4,
    "Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases|PACS1-related_disorder": 1,
    "not_provided|PACS1-related_disorder|Inborn_genetic_diseases|Schuurs-Hoeijmakers_syndrome": 1,
    "PACS1-related_disorder|Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "PACS1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Schuurs-Hoeijmakers_syndrome": 1,
    "Schuurs-Hoeijmakers_syndrome|Hypospadias": 1,
    "PACS1-related_disorder|not_provided|Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases": 1,
    "Schuurs-Hoeijmakers_syndrome|not_provided|not_specified": 2,
    "not_specified|not_provided|Schuurs-Hoeijmakers_syndrome|PACS1-related_disorder|Inborn_genetic_diseases": 1,
    "Schuurs-Hoeijmakers_syndrome|Intellectual_disability": 1,
    "PACS1-related_disorder|Schuurs-Hoeijmakers_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Schuurs-Hoeijmakers_syndrome|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|Schuurs-Hoeijmakers_syndrome": 1,
    "not_specified|not_provided|Schuurs-Hoeijmakers_syndrome": 1,
    "Spastic_paraplegia|_optic_atropy|_and_neuropathy": 1,
    "not_provided|not_specified|KLC2-related_disorder": 1,
    "KLC2-related_disorder|not_provided": 2,
    "Spastic_paraplegia|_optic_atropy|_and_neuropathy|not_provided": 2,
    "KLC2-related_disorder": 2,
    "not_provided|Spastic_paraplegia|_optic_atropy|_and_neuropathy": 1,
    "Spastic_paraplegia|_optic_atropy|_and_neuropathy|not_specified": 1,
    "TMEM151A-related_disorder": 3,
    "Episodic_kinesigenic_dyskinesia_3": 11,
    "RIN1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13": 135,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|Premature_ovarian_failure_16": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|not_specified": 6,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|B4GAT1-related_disorder|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|not_provided": 6,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|not_provided": 4,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13": 8,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|B4GAT1-related_disorder": 2,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|Inborn_genetic_diseases": 9,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|B4GAT1-related_disorder|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "B4GAT1-related_disorder": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13": 2,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|Inborn_genetic_diseases": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|B4GAT1-related_disorder": 1,
    "B4GAT1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A13|not_provided|not_specified": 1,
    "not_specified|BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder|Bardet-Biedl_syndrome": 25,
    "Bardet-Biedl_syndrome|BBS1-related_disorder|Bardet-Biedl_syndrome_1": 14,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder|Bardet-Biedl_syndrome": 9,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_1|Inborn_genetic_diseases": 5,
    "BBS1-related_disorder|not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome|BBS1-related_disorder": 21,
    "not_provided|Bardet-Biedl_syndrome|BBS1-related_disorder": 3,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|BBS1-related_disorder": 3,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Retinal_dystrophy": 2,
    "not_provided|BBS1-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder": 40,
    "BBS1-related_disorder|not_specified": 1,
    "BBS1-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 6,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder": 4,
    "BBS1-related_disorder|Bardet-Biedl_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_1|concomitant_exotropia": 1,
    "not_provided|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 3,
    "BBS1-related_disorder|Bardet-Biedl_syndrome_1": 3,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_specified": 1,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 11,
    "not_specified|Bardet-Biedl_syndrome|BBS1-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_provided": 2,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "Retinal_dystrophy|not_specified|not_provided|Bardet-Biedl_syndrome|BBS1-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|BBS1-related_disorder": 2,
    "not_specified|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|not_provided|BBS1-related_ciliopathy|BBS1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome_1": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS1-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_1|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|BBS1-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "BBS1-related_disorder|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_1": 3,
    "not_provided|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 2,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|BBS1-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Retinal_dystrophy|BBS1-related_disorder": 1,
    "BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome_1|Retinitis_pigmentosa|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Retinal_dystrophy|not_specified": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_1": 2,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS1-related_disorder": 1,
    "BBS1-related_disorder|Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder|not_provided|not_specified|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome_1|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Retinal_dystrophy|not_provided": 1,
    "not_specified|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1/7|_digenic|BBS1-related_ciliopathy|not_provided": 1,
    "Bardet-Biedl_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|BBS1-related_disorder": 2,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 3,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 4,
    "BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_1|not_specified|BBS1-related_disorder|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome_1": 1,
    "not_provided|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "not_provided|Bardet-Biedl_syndrome|BBS1-related_disorder|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 2,
    "Bardet-Biedl_syndrome|BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_1": 1,
    "not_specified|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|Retinal_dystrophy|Bardet-Biedl_syndrome": 2,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_1": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 5,
    "Bardet-Biedl_syndrome_1|Inborn_genetic_diseases|BBS1-related_disorder": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|BBS1-related_ciliopathy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 2,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_1|Retinal_dystrophy|not_specified": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 1,
    "BBS1-related_disorder|Usher_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1|Severe_early-childhood-onset_retinal_dystrophy|See_cases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|BBS1-related_ciliopathy": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Retinal_dystrophy": 1,
    "BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|BBS1-related_ciliopathy|Bardet-Biedl_syndrome_1": 1,
    "not_provided|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|not_provided": 1,
    "Bardet-Biedl_syndrome_1|BBS1-related_ciliopathy": 1,
    "BBS1-related_disorder|not_specified|Bardet-Biedl_syndrome": 1,
    "not_specified|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|BBS1-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_1|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "BBS1-related_disorder|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 2,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_1|not_provided": 1,
    "Bardet-Biedl_syndrome|BBS1-related_ciliopathy|BBS1-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome_1": 1,
    "BBS1-related_disorder|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa|BBS1-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_1|BBS1-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_1": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder": 1,
    "not_provided|BBS1-related_disorder|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_1": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_1|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|BBS1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome_1": 1,
    "ACTN3-related_disorder": 28,
    "ACTININ|_ALPHA-3_POLYMORPHISM|Actn3_deficiency|Sprinting_performance|INCREASED_COLD_TOLERANCE|not_specified": 1,
    "not_specified|ACTN3-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis_13|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13|not_provided": 5,
    "Neuronal_ceroid_lipofuscinosis_13|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13": 4,
    "Neuronal_ceroid_lipofuscinosis_13": 60,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13|not_provided|not_specified": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_13": 4,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13": 3,
    "Neuronal_ceroid_lipofuscinosis_13|CTSF-related_disorder": 3,
    "Neuronal_ceroid_lipofuscinosis_13|not_provided": 6,
    "Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases": 6,
    "not_provided|CTSF-related_disorder|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13": 1,
    "not_specified|not_provided|CTSF-related_disorder|Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases": 1,
    "not_provided|CTSF-related_disorder": 2,
    "Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis_13|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_13|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "CTSF-related_disorder": 2,
    "Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases|not_provided|CTSF-related_disorder": 1,
    "CTSF-related_disorder|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_13|not_specified": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_13|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_13|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "CTSF-related_disorder|Neuronal_ceroid_lipofuscinosis_13|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_13|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_13": 2,
    "Neuronal_ceroid_lipofuscinosis_13|Inborn_genetic_diseases|CTSF-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_13|not_provided": 1,
    "CTSF-related_disorder|Neuronal_ceroid_lipofuscinosis_13": 1,
    "CCS-related_disorder": 2,
    "Neurodegeneration": 2,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_type_5": 36,
    "Spinocerebellar_ataxia_type_5|not_provided": 7,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5": 4,
    "SPTBN2-related_disorder|Autosomal_dominant_cerebellar_ataxia|Spinocerebellar_ataxia_type_5|not_provided": 1,
    "Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5": 6,
    "Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5|not_provided": 7,
    "Autosomal_recessive_spinocerebellar_ataxia_14|not_provided": 5,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|SPTBN2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Spinocerebellar_ataxia_type_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_5|not_specified": 2,
    "not_specified|SPTBN2-related_disorder|not_provided|Autosomal_dominant_cerebellar_ataxia": 2,
    "not_specified|SPTBN2-related_disorder": 2,
    "Autosomal_dominant_cerebellar_ataxia|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5|not_provided": 1,
    "not_provided|SPTBN2-related_disorder": 7,
    "SPTBN2-related_disorder|Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5|not_specified": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_14": 14,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5": 2,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5|not_provided": 2,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5|not_provided": 2,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_14": 2,
    "Inborn_genetic_diseases|SPTBN2-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_14|not_specified|Spinocerebellar_ataxia_type_5": 1,
    "SPTBN2-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_14|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5": 1,
    "Spinocerebellar_ataxia_type_5|not_provided|Inborn_genetic_diseases": 1,
    "SPTBN2-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided": 1,
    "not_specified|not_provided|SPTBN2-related_disorder": 1,
    "SPTBN2-related_disorder|not_specified|not_provided": 1,
    "not_provided|SPTBN2-related_disorder|not_specified": 1,
    "SPTBN2-related_disorder": 5,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5": 1,
    "SPTBN2-related_disorder|not_provided": 2,
    "Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14": 1,
    "not_provided|Spinocerebellar_ataxia_type_5": 7,
    "SPTBN2-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_provided": 1,
    "SPTBN2-related_disorder|not_provided|Autosomal_dominant_cerebellar_ataxia": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14|not_specified": 2,
    "SPTBN2-related_disorder|not_provided|not_specified": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|SPTBN2-related_disorder|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|not_specified|Spinocerebellar_ataxia_type_5": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Spinocerebellar_ataxia_type_5": 1,
    "not_provided|Spinocerebellar_ataxia_type_5|Autosomal_recessive_spinocerebellar_ataxia_14": 3,
    "SPTBN2-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_dominant_cerebellar_ataxia|Autosomal_recessive_spinocerebellar_ataxia_14|Spinocerebellar_ataxia_type_5": 1,
    "not_provided|SPTBN2-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Spinocerebellar_ataxia_type_5|not_specified|Autosomal_recessive_spinocerebellar_ataxia_14|not_provided": 1,
    "not_specified|SPTBN2-related_disorder|not_provided": 2,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|Autosomal_recessive_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|SPTBN2-related_disorder": 1,
    "Spinocerebellar_ataxia_type_5|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|SPTBN2-related_disorder|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_14|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Spinocerebellar_ataxia_type_5|not_provided": 2,
    "Autosomal_dominant_cerebellar_ataxia|Autosomal_recessive_spinocerebellar_ataxia_14|not_provided": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia": 1,
    "SPTBN2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_spinocerebellar_ataxia_14": 1,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_5": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Spinocerebellar_ataxia_type_5": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_5": 1,
    "SPTBN2-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_14|not_specified|not_provided|Spinocerebellar_ataxia_type_5": 1,
    "Spinocerebellar_ataxia_type_5|not_specified": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_14|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_cerebellar_ataxia|Autosomal_recessive_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_5": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_14|not_provided|Spinocerebellar_ataxia_type_5": 1,
    "not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia|Spinocerebellar_ataxia_type_5": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|Spinocerebellar_ataxia_type_5": 1,
    "Cerebellar_ataxia|not_provided": 2,
    "TOP6BL-related_disorder": 12,
    "Hydatidiform_mole|_recurrent|_4": 3,
    "TOP6BL-related_disorder|not_provided": 1,
    "Pyruvate_carboxylase_deficiency": 1149,
    "not_provided|Pyruvate_carboxylase_deficiency": 33,
    "Pyruvate_carboxylase_deficiency|not_specified": 14,
    "not_provided|PC-related_disorder": 1,
    "not_provided|Pyruvate_carboxylase_deficiency|Inborn_genetic_diseases": 3,
    "Pyruvate_carboxylase_deficiency|PC-related_disorder": 8,
    "not_provided|Inborn_genetic_diseases|Pyruvate_carboxylase_deficiency": 4,
    "Pyruvate_carboxylase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "PC-related_disorder|not_provided|Pyruvate_carboxylase_deficiency": 3,
    "PC-related_disorder|Pyruvate_carboxylase_deficiency": 9,
    "Pyruvate_carboxylase_deficiency|Inborn_genetic_diseases": 17,
    "Inborn_genetic_diseases|Pyruvate_carboxylase_deficiency|not_provided": 5,
    "Inborn_genetic_diseases|Pyruvate_carboxylase_deficiency": 20,
    "Pyruvate_carboxylase_deficiency|not_provided|PC-related_disorder|not_specified": 1,
    "not_specified|Pyruvate_carboxylase_deficiency": 14,
    "not_provided|not_specified|Pyruvate_carboxylase_deficiency": 2,
    "not_specified|not_provided|Pyruvate_carboxylase_deficiency": 5,
    "PC-related_disorder|Pyruvate_carboxylase_deficiency|not_provided": 2,
    "Pyruvate_carboxylase_deficiency|not_provided": 27,
    "not_provided|PC-related_disorder|Pyruvate_carboxylase_deficiency": 4,
    "Pyruvate_carboxylase_deficiency|PC-related_disorder|not_provided": 2,
    "Pyruvate_carboxylase_deficiency|Inborn_genetic_diseases|not_provided": 4,
    "Pyruvate_carboxylase_deficiency|not_specified|not_provided": 5,
    "not_specified|not_provided|Pyruvate_carboxylase_deficiency|PC-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Pyruvate_carboxylase_deficiency": 4,
    "PC-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_carboxylase_deficiency": 4,
    "not_specified|Pyruvate_carboxylase_deficiency|not_provided": 3,
    "Pyruvate_carboxylase_deficiency|not_provided|not_specified": 1,
    "not_specified|PC-related_disorder|Pyruvate_carboxylase_deficiency": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Pyruvate_carboxylase_deficiency": 1,
    "not_specified|not_provided|PC-related_disorder|Pyruvate_carboxylase_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Pyruvate_carboxylase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_lactic_acidosis|Pyruvate_carboxylase_deficiency": 1,
    "KDM2A-related_neurodevelopmental_disorder": 16,
    "KDM2A-related_neurodevelopmental_disorder|Neurodevelopmental_disorder": 1,
    "KDM2A-related_neurodevelopmental_disorder|KDM2A_related_condition": 1,
    "ANKRD13D-related_condition": 1,
    "Cold-induced_sweating_syndrome_2": 5,
    "CLCF1-related_disorder": 2,
    "not_specified|RPS6KB2-related_disorder": 1,
    "RPS6KB2-related_disorder": 1,
    "not_provided|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 25,
    "Inborn_genetic_diseases|not_provided|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 1,
    "Retinal_dystrophy|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 1,
    "Cone-rod_synaptic_disorder|_congenital_nonprogressive|not_provided|Inborn_genetic_diseases": 1,
    "CABP4-related_disorder|not_provided": 4,
    "not_specified|Cone-rod_synaptic_disorder|_congenital_nonprogressive|not_provided": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 1,
    "CABP4-related_disorder|not_provided|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 3,
    "Optic_atrophy|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 2,
    "not_provided|not_specified|Retinal_dystrophy|Congenital_Stationary_Night_Blindness|_Recessive": 1,
    "not_provided|CABP4-related_disorder": 1,
    "Disorder_of_eye|Achromatopsia|not_provided|Cone-rod_dystrophy|Cone-rod_synaptic_disorder|_congenital_nonprogressive": 1,
    "Cone-rod_synaptic_disorder|_congenital_nonprogressive|Cone_dystrophy|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|not_specified|Cone-rod_dystrophy": 1,
    "Cone-rod_dystrophy|Achromatopsia|Aland_island_eye_disease": 1,
    "Hereditary_cancer-predisposing_syndrome|AIP-related_disorder": 1,
    "Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Somatotroph_adenoma|not_provided": 7,
    "Acroleukopathy|_symmetric|Pituitary_dependent_hypercortisolism|Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|AIP-related_disorder|Somatotroph_adenoma": 1,
    "Somatotroph_adenoma|Pituitary_adenoma_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "AIP-related_disorder|Familial_isolated_pituitary_adenoma|Hereditary_cancer-predisposing_syndrome|not_provided|Somatotroph_adenoma": 1,
    "not_provided|AIP-related_disorder|Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma": 18,
    "Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma|not_provided": 8,
    "Hereditary_cancer-predisposing_syndrome|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|AIP-related_disorder|Pituitary_adenoma_5|_multiple_types|not_provided": 1,
    "not_provided|Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome": 12,
    "Somatotroph_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome|not_provided": 13,
    "not_specified|not_provided|Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Somatotroph_adenoma": 15,
    "Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma|not_provided|AIP-related_disorder": 1,
    "AIP-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_isolated_pituitary_adenoma|not_provided": 1,
    "Somatotroph_adenoma|AIP-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pituitary_dependent_hypercortisolism|Somatotroph_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Somatotroph_adenoma": 1,
    "Familial_isolated_pituitary_adenoma|not_provided|Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Somatotroph_adenoma|Pituitary_dependent_hypercortisolism|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|AIP-related_disorder": 3,
    "Familial_isolated_pituitary_adenoma|not_provided": 1,
    "Somatotroph_adenoma|AIP-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|Somatotroph_adenoma": 2,
    "Hereditary_cancer-predisposing_syndrome|AIP-related_disorder|not_provided|Somatotroph_adenoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|AIP-related_disorder|Somatotroph_adenoma": 1,
    "not_provided|AIP-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Pituitary_adenoma_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_isolated_pituitary_adenoma": 1,
    "Familial_isolated_pituitary_adenoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Somatotroph_adenoma": 1,
    "Somatotroph_adenoma|Familial_isolated_pituitary_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "AIP-related_disorder|Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma|not_provided": 2,
    "not_provided|Familial_isolated_pituitary_adenoma": 1,
    "not_provided|Somatotroph_adenoma|Pituitary_adenoma_predisposition": 1,
    "AIP-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Somatotroph_adenoma": 3,
    "Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma|Familial_isolated_pituitary_adenoma|not_provided": 1,
    "not_provided|Somatotroph_adenoma|Pituitary_dependent_hypercortisolism|Acroleukopathy|_symmetric|Hereditary_cancer-predisposing_syndrome": 1,
    "AIP-related_disorder|Somatotroph_adenoma|Familial_isolated_pituitary_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "AIP-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Somatotroph_adenoma|Pituitary_dependent_hypercortisolism|Dopamine_agonists_response": 1,
    "not_provided|Somatotroph_adenoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "AIP-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma|not_provided|Familial_isolated_pituitary_adenoma": 1,
    "Familial_isolated_pituitary_adenoma|not_provided|Hereditary_cancer-predisposing_syndrome|Somatotroph_adenoma": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|CABP2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_93": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_93|Nonsyndromic_genetic_hearing_loss|not_specified|not_provided": 1,
    "CABP2-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_93": 4,
    "CABP2-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_93": 1,
    "Inborn_genetic_diseases|Autism": 1,
    "CABP2-related_disorder|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_93": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_93|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|CABP2-related_disorder|not_specified": 1,
    "CABP2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_93": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_93": 1,
    "not_provided|CABP2-related_disorder": 1,
    "Abnormality_of_immune_system_physiology|not_provided": 1,
    "Kala-azar_susceptibility_2": 1,
    "not_provided|Pulmonary_disease|_chronic_obstructive|_susceptibility_to": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|NDUFV1-related_disorder": 1,
    "not_provided|NDUFV1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_specified": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 7,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|not_provided": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_specified|NDUFV1-related_disorder|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided|Leigh_syndrome": 3,
    "not_provided|NDUFV1-related_disorder|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_specified": 1,
    "NDUFV1-related_disorder|not_provided": 4,
    "NDUFV1-related_disorder|not_specified|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|Leigh_syndrome|not_provided": 1,
    "NDUFV1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|not_specified": 1,
    "not_provided|NDUFV1-related_disorder": 6,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|See_cases": 1,
    "not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_5|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided": 2,
    "NDUFV1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "not_specified|Leigh_syndrome|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_4|Leigh_syndrome": 1,
    "Leigh_syndrome|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "Inborn_genetic_diseases|NDUFV1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_4|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "not_specified|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_specified|not_provided": 1,
    "Leigh_syndrome|NDUFV1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|Leigh_syndrome|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_4": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_4|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type|NDUFV1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_4|Leigh_syndrome": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_4|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_4|not_provided": 1,
    "TBX10-related_disorder": 14,
    "Mendelian_syndromes_with_cleft_lip/palate|TBX10-related_disorder": 1,
    "TBX10-related_disorder|not_provided": 1,
    "Immunodeficiency": 632,
    "Type_1_interferonopathy": 1,
    "UNC93B1-related_disorder": 1,
    "UNC93B1-related_disorder|Herpes_simplex_encephalitis|_susceptibility_to|_1": 2,
    "not_provided|not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_1": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_1|UNC93B1-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFS8-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_2|Inborn_genetic_diseases|not_provided|Leigh_syndrome": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_2": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_2": 13,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_2": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_2|not_provided": 4,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_2|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided|Leigh_syndrome|NDUFS8-related_disorder": 1,
    "not_provided|NDUFS8-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_2": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_2|Inborn_genetic_diseases": 1,
    "NDUFS8-related_disorder|not_provided": 1,
    "not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_specified|not_provided|NDUFS8-related_disorder|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "NDUFS8-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|Mitochondrial_complex_I_deficiency|not_provided|Osteopetrosis": 2,
    "Autosomal_recessive_osteopetrosis_1": 168,
    "Autosomal_recessive_osteopetrosis_1|not_provided": 85,
    "not_provided|Autosomal_recessive_osteopetrosis_1|TCIRG1-related_disorder": 6,
    "TCIRG1-related_disorder|not_provided|Autosomal_recessive_osteopetrosis_1": 9,
    "not_provided|Autosomal_recessive_osteopetrosis_1|Mitochondrial_complex_I_deficiency|_nuclear_type_2": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_1": 123,
    "not_provided|Autosomal_recessive_osteopetrosis_1|Inborn_genetic_diseases": 11,
    "TCIRG1-related_disorder|not_provided|Autosomal_recessive_osteopetrosis|Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_1": 1,
    "Autosomal_recessive_osteopetrosis_1|TCIRG1-related_disorder|not_provided": 6,
    "Autosomal_recessive_osteopetrosis_1|not_provided|TCIRG1-related_disorder": 2,
    "TCIRG1-related_disorder": 4,
    "Increased_bone_mineral_density|not_specified|Autosomal_recessive_osteopetrosis_1|not_provided": 1,
    "Autosomal_recessive_osteopetrosis_1|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Osteopetrosis|Autosomal_recessive_osteopetrosis_1": 2,
    "not_provided|not_specified|Autosomal_recessive_osteopetrosis_1": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_1|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_1|TCIRG1-related_disorder|not_provided": 1,
    "TCIRG1-related_disorder|Autosomal_recessive_osteopetrosis_1|not_provided": 3,
    "not_specified|not_provided|Autosomal_recessive_osteopetrosis_1": 4,
    "Autosomal_recessive_osteopetrosis_1|not_specified": 2,
    "Autosomal_recessive_osteopetrosis_1|not_specified|not_provided": 2,
    "Autosomal_recessive_osteopetrosis_1|Osteopetrosis|not_provided": 4,
    "TCIRG1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Osteopetrosis": 26,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_1": 2,
    "not_provided|TCIRG1-related_disorder": 5,
    "Chorea-acanthocytosis|not_provided|Autosomal_recessive_osteopetrosis_1": 1,
    "Autosomal_recessive_osteopetrosis_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_1": 1,
    "TCIRG1-related_disorder|not_provided": 6,
    "not_provided|Autosomal_recessive_osteopetrosis_1|Osteopetrosis": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_osteopetrosis_1": 3,
    "Osteopetrosis|not_provided|Autosomal_recessive_osteopetrosis_1": 3,
    "TCIRG1-related_disorder|not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Autosomal_recessive_osteopetrosis_1|Increased_bone_mineral_density": 1,
    "Autosomal_recessive_osteopetrosis_1|TCIRG1-related_disorder": 3,
    "not_provided|Autosomal_recessive_osteopetrosis_1|Decreased_total_neutrophil_count": 2,
    "Abnormality_of_the_skeletal_system|Osteopetrosis|Autosomal_recessive_osteopetrosis_1|not_provided": 1,
    "Autosomal_recessive_osteopetrosis_1|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_osteopetrosis_1|not_specified|Increased_bone_mineral_density|not_provided": 1,
    "TCIRG1-related_disorder|not_provided|Autosomal_recessive_osteopetrosis_1|Osteopetrosis": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|TCIRG1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|TCIRG1-related_disorder": 1,
    "Dysosteosclerosis": 1,
    "Decreased_total_neutrophil_count": 2,
    "not_specified|Autosomal_recessive_osteopetrosis_1|not_provided|TCIRG1-related_disorder": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Congenital_neutropenia": 1,
    "Inborn_genetic_diseases|TCIRG1-related_disorder": 1,
    "not_specified|Autosomal_recessive_osteopetrosis_1": 1,
    "TCIRG1-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_osteopetrosis_1": 1,
    "not_provided|Decreased_total_neutrophil_count": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_movement_abnormalities|_and_seizures|Intellectual_disability|_severe|Microcephaly|Seizure": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_movement_abnormalities|_and_seizures|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_movement_abnormalities|_and_seizures": 3,
    "Seizure|Intellectual_disability|_severe|Microcephaly|Neurodevelopmental_disorder_with_microcephaly|_movement_abnormalities|_and_seizures": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_movement_abnormalities|_and_seizures|Seizure|Intellectual_disability|_severe|Microcephaly": 1,
    "Intellectual_disability|_autosomal_dominant_51": 53,
    "Intellectual_disability|_autosomal_dominant_51|not_provided": 5,
    "not_provided|KMT5B-related_disorder": 8,
    "KMT5B-related_disorder": 11,
    "not_provided|Intellectual_disability|_autosomal_dominant_51": 4,
    "Inborn_genetic_diseases|not_provided|KMT5B-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|KMT5B-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_51": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|KMT5B-related_disorder": 1,
    "KMT5B-related_disorder|not_provided": 2,
    "KMT5B-related_neurodevelopmental_disorder": 1,
    "Language_retardation": 1,
    "Intellectual_disability|_autosomal_dominant_51|Autism_spectrum_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_51|Neural_tube_defect": 1,
    "Intellectual_disability|_autosomal_dominant_51|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autistic_behavior": 1,
    "KMT5B-related_disorder|Intellectual_disability|_autosomal_dominant_51": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta": 2,
    "Osteoporosis_with_pseudoglioma": 21,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Retinal_dystrophy|Osteoporosis_with_pseudoglioma|Optic_atrophy|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|LRP5-related_disorder|not_specified|Retinal_dystrophy|Osteogenesis_imperfecta|not_provided": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided": 25,
    "Autosomal_dominant_polycystic_liver_disease|not_specified|not_provided|Osteogenesis_imperfecta|Increased_bone_mineral_density": 1,
    "Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided": 16,
    "Inborn_genetic_diseases|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided|not_specified": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 8,
    "not_provided|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|LRP5-related_disorder": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma": 62,
    "LRP5-related_disorder": 14,
    "Osteogenesis_imperfecta|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_provided": 1,
    "LRP5-related_disorder|not_provided": 19,
    "not_provided|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4": 1,
    "not_provided|LRP5-related_disorder": 26,
    "Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4": 11,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided": 20,
    "Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|not_specified|not_provided": 1,
    "Bone_mineral_density_quantitative_trait_locus_1": 2,
    "not_provided|Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 10,
    "Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4": 7,
    "not_provided|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 8,
    "Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|not_provided": 14,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided|Retinal_dystrophy": 1,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 8,
    "Exudative_vitreoretinopathy_4|not_provided": 4,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "not_provided|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 5,
    "Exudative_vitreoretinopathy_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Osteoporosis|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_4": 16,
    "not_provided|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma": 6,
    "Worth_disease": 2,
    "not_provided|Osteoporosis_with_pseudoglioma": 5,
    "not_provided|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_1|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_provided": 1,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided": 8,
    "Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|not_provided": 9,
    "Exudative_vitreoretinopathy_4|_autosomal_dominant|Osteoporosis_with_pseudoglioma": 1,
    "not_provided|Exudative_vitreoretinopathy_4": 4,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma": 10,
    "Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|not_provided": 7,
    "Autosomal_dominant_osteopetrosis_1": 3,
    "Increased_bone_mineral_density|not_provided|High_bone_mass": 1,
    "LRP5-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided": 1,
    "Osteogenesis_imperfecta|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided|Osteogenesis_imperfecta": 1,
    "Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided|LRP5-related_disorder|Inborn_genetic_diseases": 1,
    "High_bone_mass": 1,
    "Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|not_provided": 2,
    "not_provided|Autosomal_dominant_osteopetrosis_1|Worth_disease": 1,
    "not_provided|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 12,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|LRP5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 2,
    "not_specified|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "not_specified|not_provided|Increased_bone_mineral_density": 1,
    "not_provided|Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1": 5,
    "LRP5-related_disorder|not_provided|Skeletal_dysplasia|Autosomal_dominant_osteopetrosis_1|Worth_disease": 1,
    "not_provided|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1": 7,
    "not_specified|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Exudative_vitreoretinopathy_4|_autosomal_recessive": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Autosomal_dominant_osteopetrosis_1": 1,
    "Inborn_genetic_diseases|not_provided|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "Osteoporosis|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|LRP5-related_disorder": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|not_provided": 19,
    "Osteoporosis|not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Osteoporosis_with_pseudoglioma|not_provided": 4,
    "Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|LRP5-related_disorder|Osteogenesis_imperfecta|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 1,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|not_specified": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|not_provided": 4,
    "Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 3,
    "Exudative_vitreoretinopathy_4|not_provided|Osteogenesis_imperfecta": 1,
    "Inborn_genetic_diseases|not_provided|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_1|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|not_specified": 1,
    "Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteogenesis_imperfecta|not_provided": 1,
    "not_specified|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_4|Retinal_dystrophy": 1,
    "Worth_disease|Exudative_vitreoretinopathy_4|Osteoporosis|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_1|LRP5-related_disorder|not_provided": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided|Inborn_genetic_diseases": 1,
    "LRP5-related_disorder|not_specified|not_provided": 3,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided|LRP5-related_disorder|Retinal_dystrophy": 1,
    "LRP5-related_primary_osteoporosis": 2,
    "Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|not_provided": 1,
    "not_provided|LRP5-related_disorder|Exudative_vitreoretinopathy_4|_digenic": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided|not_specified": 1,
    "LRP5-related_disorder|not_provided|Osteoporosis_with_pseudoglioma": 1,
    "Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Retinal_dystrophy|not_provided|Osteogenesis_imperfecta|Polycystic_liver_disease_1": 1,
    "Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|not_provided": 1,
    "Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Autosomal_dominant_osteopetrosis_1|not_provided|Osteogenesis_imperfecta": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_1|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|not_specified|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_1": 25,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma": 4,
    "Osteoporosis_with_pseudoglioma|Retinal_dystrophy|not_specified|not_provided|LRP5-related_disorder": 1,
    "Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Osteoporosis_with_pseudoglioma|Worth_disease|Exudative_vitreoretinopathy_4|LRP5-related_disorder|not_provided|Exudative_vitreoretinopathy_1": 1,
    "Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|not_provided|Inborn_genetic_diseases": 2,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|LRP5-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided": 2,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_1|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis|not_provided": 1,
    "Worth_disease|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|not_provided": 1,
    "Diaphyseal_dysplasia|Brachycephaly|Decreased_circulating_vitamin_D_concentration|Diaphyseal_sclerosis|Elevated_circulating_alkaline_phosphatase_concentration|Hypoplastic_acetabulae|Osteopenia": 1,
    "Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Retinal_dystrophy|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|not_provided|not_specified": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases": 1,
    "Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Autosomal_dominant_polycystic_liver_disease|not_provided|Leber_congenital_amaurosis": 1,
    "Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Worth_disease|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "LRP5-related_disorder|not_provided|Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1": 2,
    "not_provided|Osteoporosis_with_pseudoglioma|Osteogenesis_imperfecta": 1,
    "not_provided|Retinal_dystrophy|Exudative_vitreoretinopathy_4|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Worth_disease|LRP5-related_disorder|not_provided": 1,
    "not_provided|not_specified|LRP5-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Exudative_vitreoretinopathy_4|_autosomal_recessive": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_polycystic_liver_disease": 2,
    "not_provided|not_specified|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 1,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|not_provided": 1,
    "Osteoporosis|Worth_disease|Exudative_vitreoretinopathy_1|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Exudative_vitreoretinopathy_4|not_specified|not_provided": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|LRP5-related_exudative_vitreoretinopathy|not_provided": 1,
    "Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|LRP5-related_disorder|not_provided|Microcephaly": 1,
    "Osteoporosis|Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Worth_disease|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Retinal_dystrophy|not_specified|not_provided|Osteogenesis_imperfecta|Increased_bone_mineral_density": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_provided|Osteogenesis_imperfecta": 1,
    "Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|not_provided": 2,
    "Vitreoretinopathy|Retinal_dystrophy": 1,
    "not_specified|not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|LRP5-related_disorder": 1,
    "Osteogenesis_imperfecta|LRP5-related_disorder|not_provided": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided": 1,
    "Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis|not_provided|not_specified": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4": 10,
    "not_provided|LRP5-related_disorder|Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|not_specified": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Exudative_vitreoretinopathy_4": 1,
    "Osteoporosis|Worth_disease|Exudative_vitreoretinopathy_1|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Exudative_vitreoretinopathy_4|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|LRP5-related_disorder|not_provided": 1,
    "not_specified|Osteogenesis_imperfecta|Increased_bone_mineral_density|not_provided|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_4|_autosomal_recessive": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis|not_provided|LRP5-related_disorder": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|LRP5-related_disorder": 2,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|not_provided": 5,
    "Inborn_genetic_diseases|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 1,
    "Exudative_vitreoretinopathy_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 1,
    "Inborn_genetic_diseases|not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma": 1,
    "not_provided|Osteoporosis_with_pseudoglioma|Worth_disease|Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1": 1,
    "Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|LRP5-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided|LRP5-related_disorder": 1,
    "Inborn_genetic_diseases|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_specified|not_provided": 2,
    "not_provided|Worth_disease|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|LRP5-related_disorder": 1,
    "not_provided|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Postmenopausal_osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|Van_Buchem_disease_type_2|LRP5-related_disorder": 1,
    "Retinal_dystrophy|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Exudative_vitreoretinopathy_4": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis|Worth_disease|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|not_specified|not_provided": 1,
    "Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided|Osteoporosis|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Osteoporosis|Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|LRP5-related_disorder": 1,
    "not_specified|not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma": 1,
    "Inborn_genetic_diseases|Worth_disease|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta|Severe_early-childhood-onset_retinal_dystrophy": 1,
    "Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_provided|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "LRP5-related_disorder|Osteoporosis_with_pseudoglioma|Postmenopausal_osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Exudative_vitreoretinopathy_4|Van_Buchem_disease_type_2|Exudative_vitreoretinopathy_1|Bone_mineral_density_quantitative_trait_locus_1|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Osteogenesis_imperfecta|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Worth_disease|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteogenesis_imperfecta": 1,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Worth_disease|Inborn_genetic_diseases": 1,
    "not_provided|Worth_disease|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Exudative_vitreoretinopathy_1": 1,
    "not_specified|not_provided|LRP5-related_disorder|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 1,
    "not_specified|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_1|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_provided": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|not_provided": 1,
    "not_provided|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|LRP5-related_disorder": 1,
    "Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases|LRP5-related_disorder|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|Retinal_dystrophy": 1,
    "LRP5-related_disorder|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|LRP5-related_disorder|not_provided": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|not_specified|not_provided": 1,
    "not_provided|LRP5-related_disorder|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta|LRP5-related_disorder": 1,
    "Osteoporosis|Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Autosomal_dominant_osteopetrosis_1|not_provided|Polycystic_liver_disease_1": 1,
    "Inborn_genetic_diseases|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|not_provided": 1,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Osteoporosis|Exudative_vitreoretinopathy_1|Inborn_genetic_diseases": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteogenesis_imperfecta": 1,
    "Retinal_dystrophy|not_provided|Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 1,
    "not_provided|Osteogenesis_imperfecta|Inborn_genetic_diseases": 2,
    "not_provided|Polycystic_liver_disease_1|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Bone_mineral_density_quantitative_trait_locus_1": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|not_provided|LRP5-related_disorder": 3,
    "not_provided|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4": 1,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 1,
    "not_provided|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1": 5,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|LRP5-related_disorder|not_provided": 1,
    "Exudative_vitreoretinopathy_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1": 1,
    "Inborn_genetic_diseases|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "not_specified|not_provided|Increased_bone_mineral_density|Osteogenesis_imperfecta|Osteoporosis_with_pseudoglioma": 1,
    "Osteogenesis_imperfecta|Increased_bone_mineral_density|not_provided|not_specified": 2,
    "not_provided|not_specified|Osteogenesis_imperfecta|Increased_bone_mineral_density": 1,
    "not_specified|Osteogenesis_imperfecta|Increased_bone_mineral_density|not_provided": 1,
    "Autosomal_dominant_polycystic_liver_disease|Inborn_genetic_diseases|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Retinal_dystrophy|Exudative_vitreoretinopathy_4|_autosomal_recessive": 1,
    "LRP5-related_disorder|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_4|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_provided|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Osteoporosis": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|LRP5-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta|not_provided|not_specified": 3,
    "not_provided|Autosomal_dominant_polycystic_liver_disease|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|LRP5-related_disorder": 1,
    "not_provided|LRP5-related_disorder|Osteogenesis_imperfecta": 1,
    "Autosomal_dominant_polycystic_liver_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|not_provided": 1,
    "not_specified|not_provided|LRP5-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4": 1,
    "Exudative_vitreoretinopathy_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Exudative_vitreoretinopathy_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_provided|Inborn_genetic_diseases": 1,
    "Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis_with_pseudoglioma|Autosomal_dominant_osteopetrosis_1|not_provided|not_specified": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|not_specified|not_provided": 1,
    "Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Van_Buchem_disease_type_2|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_1|LRP5-related_primary_osteoporosis": 1,
    "Worth_disease|Osteoporosis|Autosomal_dominant_osteopetrosis_1|Exudative_vitreoretinopathy_1|Bone_mineral_density_quantitative_trait_locus_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_4|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_1|not_provided|LRP5-related_disorder|Inborn_genetic_diseases": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases": 1,
    "not_provided|Exudative_vitreoretinopathy_4|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Bone_mineral_density_quantitative_trait_locus_1|Osteoporosis|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|not_specified|Osteogenesis_imperfecta": 1,
    "Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4|Retinal_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Familial_exudative_vitreoretinopathy|not_provided|Exudative_vitreoretinopathy_4|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_4|_autosomal_dominant": 1,
    "LRP5-related_disorder|Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Worth_disease|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "not_specified|LRP5-related_disorder|not_provided": 1,
    "Osteoporosis_with_pseudoglioma|Inborn_genetic_diseases|not_provided": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Exudative_vitreoretinopathy_4|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|not_provided": 1,
    "Worth_disease|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Autosomal_dominant_osteopetrosis_1|Exudative_vitreoretinopathy_1|Osteoporosis_with_pseudoglioma|Exudative_vitreoretinopathy_4|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided|Exudative_vitreoretinopathy_1|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Osteoporosis|Exudative_vitreoretinopathy_4": 1,
    "Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_1|Exudative_vitreoretinopathy_4|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|not_provided": 1,
    "Polycystic_liver_disease_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts": 1,
    "not_specified|Osteoporosis_with_pseudoglioma|Microcephaly|not_provided": 1,
    "Bone_mineral_density_quantitative_trait_locus_1|Exudative_vitreoretinopathy_4|Worth_disease|Autosomal_dominant_osteopetrosis_1|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Osteoporosis_with_pseudoglioma|POLYCYSTIC_LIVER_DISEASE_4_WITH_KIDNEY_CYSTS|not_provided|Polycystic_liver_disease_1": 1,
    "not_provided|Autosomal_dominant_osteopetrosis_1|Osteoporosis_with_pseudoglioma|Polycystic_liver_disease_4_with_or_without_kidney_cysts|Bone_mineral_density_quantitative_trait_locus_1|Worth_disease|Exudative_vitreoretinopathy_4|Inborn_genetic_diseases": 1,
    "LRP5-related_disorder|Osteogenesis_imperfecta": 1,
    "Familial_temporal_lobe_epilepsy_8": 35,
    "not_specified|Familial_temporal_lobe_epilepsy_8": 7,
    "Familial_temporal_lobe_epilepsy_8|not_specified": 4,
    "not_provided|Familial_temporal_lobe_epilepsy_8|GAL-related_disorder": 1,
    "not_provided|Familial_temporal_lobe_epilepsy_8": 1,
    "Familial_temporal_lobe_epilepsy_8|GAL-related_disorder|not_provided": 1,
    "Familial_temporal_lobe_epilepsy_8|not_provided": 3,
    "GAL-related_disorder|Familial_temporal_lobe_epilepsy_8": 1,
    "Carnitine_palmitoyl_transferase_1A_deficiency": 860,
    "Carnitine_palmitoyl_transferase_1A_deficiency|Inborn_genetic_diseases": 15,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_provided": 26,
    "not_specified|Carnitine_palmitoyl_transferase_1A_deficiency": 11,
    "not_provided|Carnitine_palmitoyl_transferase_1A_deficiency": 10,
    "Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_1A_deficiency": 27,
    "CPT1A-related_disorder|not_provided|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_specified": 10,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_specified|not_provided": 6,
    "not_specified|Carnitine_palmitoyl_transferase_1A_deficiency|CPT1A-related_disorder": 1,
    "CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency": 8,
    "not_specified|not_provided|CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "not_provided|not_specified|Carnitine_palmitoyl_transferase_1A_deficiency": 3,
    "Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_1A_deficiency|not_provided": 2,
    "not_specified|Carnitine_palmitoyl_transferase_1A_deficiency|CPT1A-related_disorder|not_provided": 1,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_specified|CPT1A-related_disorder": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "not_specified|Carnitine_palmitoyl_transferase_1A_deficiency|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "CPT1A-related_disorder|CPT1A_POLYMORPHISM|CPT1A_ARCTIC_VARIANT|Inborn_genetic_diseases|Carnitine_palmitoyl_transferase_1A_deficiency|not_provided": 1,
    "not_specified|Carnitine_palmitoyl_transferase_1A_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency": 2,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_provided|CPT1A-related_disorder": 2,
    "Carnitine_palmitoyl_transferase_1A_deficiency|not_provided|not_specified": 2,
    "CPT1A-related_disorder|not_specified|not_provided|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "not_provided|CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency": 1,
    "Carnitine_palmitoyl_transferase_1A_deficiency|CPT1A-related_disorder": 3,
    "Carnitine_palmitoyl_transferase_1A_deficiency|CPT1A-related_disorder|not_specified": 1,
    "not_provided|CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency|not_specified": 1,
    "CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency|Inborn_genetic_diseases": 1,
    "CPT1A-related_disorder|not_provided": 1,
    "Carnitine_palmitoyl_transferase_1A_deficiency|Inborn_genetic_diseases|CPT1A-related_disorder|not_provided": 1,
    "CPT1A-related_disorder": 2,
    "CPT1A-related_disorder|Carnitine_palmitoyl_transferase_1A_deficiency|not_provided": 1,
    "Metabolic_disease": 3,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 3,
    "not_specified|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 17,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 436,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 283,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 12,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1": 46,
    "Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 6,
    "Charcot-Marie-Tooth_disease|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Ptosis|Severe_muscular_hypotonia|Tachypnea|Clonus|Hyperreflexia|Failure_to_thrive|Respiratory_distress": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Distal_spinal_muscular_atrophy|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 5,
    "IGHMBP2-related_disorder|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|Peripheral_neuropathy|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "Charcot-Marie-Tooth_disease|IGHMBP2-related_disorder|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_specified|not_provided": 3,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 15,
    "Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Lower_limb_muscle_weakness|Difficulty_walking|Inability_to_walk|Hammertoe|Progressive_muscle_weakness|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 24,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 7,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 12,
    "IGHMBP2-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 6,
    "not_provided|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "IGHMBP2-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "IGHMBP2-related_disorder|not_provided|Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|not_provided": 6,
    "IGHMBP2-related_disorder|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases": 15,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified": 6,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|IGHMBP2-related_disorder|Charcot-Marie-Tooth_disease|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified": 3,
    "IGHMBP2-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 14,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_provided": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2S|Spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|IGHMBP2-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 17,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S": 5,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|IGHMBP2-related_disorder|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 2,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 3,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 4,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|IGHMBP2-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|not_provided": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 3,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 15,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "not_provided|Distal_spinal_muscular_atrophy|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|Lower_limb_muscle_weakness|Difficulty_walking|Inability_to_walk|Hammertoe|Progressive_muscle_weakness|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided|IGHMBP2-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|IGHMBP2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Distal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|IGHMBP2-related_disorder": 1,
    "IGHMBP2-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases|not_provided": 6,
    "Inborn_genetic_diseases|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided": 2,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "IGHMBP2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "IGHMBP2-related_disorder": 2,
    "not_provided|IGHMBP2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2S|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|not_provided": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Neurodevelopmental_disorder|IGHMBP2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|IGHMBP2-related_disorder": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|not_provided|Charcot-Marie-Tooth_disease": 2,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|IGHMBP2-related_disorder": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Distal_spinal_muscular_atrophy": 1,
    "Distal_spinal_muscular_atrophy|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|not_provided": 2,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Peripheral_neuropathy|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Neuronopathy|_distal_hereditary_motor|_type_2C|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Distal_spinal_muscular_atrophy|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Distal_spinal_muscular_atrophy|not_provided": 1,
    "Distal_spinal_muscular_atrophy|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|IGHMBP2-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified": 1,
    "Autosomal_dominant_intermediate_Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|Inborn_genetic_diseases": 1,
    "IGHMBP2-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Distal_spinal_muscular_atrophy": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|See_cases|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease": 1,
    "Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|Charcot-Marie-Tooth_disease|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease": 1,
    "IGHMBP2-related_disorder|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "not_specified|Charcot-Marie-Tooth_disease|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Distal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2S|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|Charcot-Marie-Tooth_disease_axonal_type_2S|Charcot-Marie-Tooth_disease|IGHMBP2-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|IGHMBP2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 1,
    "not_specified|Autosomal_recessive_distal_spinal_muscular_atrophy_1|not_provided": 1,
    "not_provided|Autosomal_recessive_distal_spinal_muscular_atrophy_1": 5,
    "MRGPRF-related_condition": 1,
    "SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_10|not_specified": 1,
    "SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_10": 3,
    "TPCN2-related_condition|not_specified": 1,
    "TPCN2-related_condition": 2,
    "Von_Hippel-Lindau_syndrome|Multiple_myeloma|Colorectal_cancer": 1,
    "CCND1-related_disorder": 3,
    "CCND1-related_disorder|not_provided": 1,
    "not_provided|MULTIPLE_MYELOMA|_t(11%3B14)_TYPE|_SUSCEPTIBILITY_TO|VON_HIPPEL-LINDAU_SYNDROME|_MODIFIER_OF|CCND1-related_disorder|Colorectal_cancer|_susceptibility_to": 1,
    "Thoracic_dysostosis|_isolated|not_provided": 1,
    "Thoracic_dysostosis|_isolated": 1,
    "not_provided|FGF3-related_disorder": 4,
    "Deafness_with_labyrinthine_aplasia|_microtia|_and_microdontia|not_provided": 3,
    "Deafness_with_labyrinthine_aplasia|_microtia|_and_microdontia": 23,
    "Deafness_with_labyrinthine_aplasia|_microtia|_and_microdontia|Hearing_impairment": 1,
    "FGF3-related_disorder": 2,
    "not_provided|Deafness_with_labyrinthine_aplasia|_microtia|_and_microdontia|FGF3-related_disorder": 1,
    "FGF3-related_disorder|not_provided|Deafness_with_labyrinthine_aplasia|_microtia|_and_microdontia": 1,
    "not_provided|Deafness_with_labyrinthine_aplasia|_microtia|_and_microdontia": 2,
    "not_specified|Moyamoya_disease_7": 1,
    "Intestinal_dysmotility_syndrome|not_provided": 1,
    "ANO1-related_fatal_neonatal_disease_due_to_impaired_chloride_currents": 1,
    "Moyamoya_disease_7": 3,
    "FADD-related_immunodeficiency": 114,
    "FADD-related_immunodeficiency|not_specified": 1,
    "Inborn_genetic_diseases|FADD-related_immunodeficiency": 3,
    "FADD-related_immunodeficiency|not_provided": 2,
    "not_provided|FADD-related_immunodeficiency": 3,
    "FADD-related_immunodeficiency|Inborn_genetic_diseases": 2,
    "FADD-related_disorder|FADD-related_immunodeficiency": 1,
    "not_specified|FADD-related_immunodeficiency|not_provided": 1,
    "PPFIA1-related_disorder": 26,
    "SHANK2-related_disorder": 38,
    "Autism|_susceptibility_to|_17|not_provided": 3,
    "Autism|_susceptibility_to|_17": 29,
    "not_provided|Autism|_susceptibility_to|_17": 4,
    "not_specified|not_provided|Autism|_susceptibility_to|_17": 1,
    "Autism_spectrum_disorder|not_provided|Autism|_susceptibility_to|_17": 1,
    "not_provided|Autism|_susceptibility_to|_17|not_specified": 1,
    "Rare_disease_with_autism": 1,
    "Intellectual_disability|Autism_spectrum_disorder|Schizophrenia": 1,
    "SHANK2-related_disorder|Complex_neurodevelopmental_disorder|not_specified|not_provided": 1,
    "not_specified|Autism|_susceptibility_to|_17": 1,
    "Autism|_susceptibility_to|_17|Intellectual_disability|not_provided": 1,
    "not_specified|not_provided|Autism": 1,
    "Autism|_susceptibility_to|_17|Intellectual_disability": 1,
    "not_specified|Autism|_susceptibility_to|_17|not_provided": 1,
    "SHANK2-related_Complex_neurodevelopmental_disorder": 1,
    "not_provided|Autism_spectrum_disorder|Rare_disease_with_autism": 1,
    "SHANK2-related_disorder|not_provided": 1,
    "Autism_spectrum_disorder|SHANK2-related_disorder": 1,
    "See_cases|Autism_spectrum_disorder": 1,
    "not_specified|not_provided|Autism|_susceptibility_to|_17|Inborn_genetic_diseases": 1,
    "not_provided|Autism_spectrum_disorder|SHANK2-related_disorder": 2,
    "Autism_spectrum_disorder|Autism|_susceptibility_to|_17": 1,
    "Neurodevelopmental_disorder|Autism|_susceptibility_to|_17": 1,
    "Autism_spectrum_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Autism_spectrum_disorder|not_provided|SHANK2-related_disorder": 1,
    "Autism|_susceptibility_to|_17|Inborn_genetic_diseases": 1,
    "not_specified|SHANK2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autism|_susceptibility_to|_17": 1,
    "Autism_spectrum_disorder|Inborn_genetic_diseases|Intellectual_disability|not_provided": 1,
    "Inborn_genetic_diseases|SHANK2-related_disorder": 1,
    "not_provided|SHANK2-related_disorder": 1,
    "Smith-Lemli-Opitz_syndrome": 685,
    "Smith-Lemli-Opitz_syndrome|not_provided": 38,
    "not_provided|Smith-Lemli-Opitz_syndrome": 33,
    "DHCR7-related_disorder": 6,
    "not_provided|Smith-Lemli-Opitz_syndrome|not_specified": 2,
    "DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome": 11,
    "not_provided|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome": 18,
    "not_provided|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder": 1,
    "Smith-Lemli-Opitz_syndrome|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Smith-Lemli-Opitz_syndrome": 10,
    "not_provided|Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome": 2,
    "not_specified|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Smith-Lemli-Opitz_syndrome": 9,
    "Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|DHCR7-related_disorder|not_provided": 1,
    "not_provided|not_specified|Smith-Lemli-Opitz_syndrome": 4,
    "Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome|not_provided": 5,
    "not_specified|not_provided|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases": 2,
    "Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|not_provided": 2,
    "not_specified|not_provided|Smith-Lemli-Opitz_syndrome": 5,
    "DHCR7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Smith-Lemli-Opitz_syndrome": 5,
    "not_provided|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases": 7,
    "Smith-Lemli-Opitz_syndrome|not_provided|Inborn_genetic_diseases": 9,
    "not_provided|DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome": 2,
    "Smith-Lemli-Opitz_syndrome|not_specified": 2,
    "DHCR7-related_disorder|not_specified|Smith-Lemli-Opitz_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|DHCR7-related_disorder": 3,
    "Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder": 8,
    "Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "DHCR7-related_disorder|Inborn_genetic_diseases|not_provided|Smith-Lemli-Opitz_syndrome": 7,
    "Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases": 7,
    "DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome|not_specified|not_provided": 2,
    "not_provided|DHCR7-related_disorder": 1,
    "Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|not_specified": 1,
    "not_specified|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "DHCR7-related_disorder|Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome|not_specified|not_provided": 1,
    "not_specified|Smith-Lemli-Opitz_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Smith-Lemli-Opitz_syndrome": 11,
    "DHCR7-related_disorder|not_provided|Smith-Lemli-Opitz_syndrome|Microcephaly": 1,
    "Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|not_provided": 7,
    "not_specified|Hepatoblastoma|not_provided|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder": 1,
    "not_specified|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DHCR7-related_disorder|not_provided|Smith-Lemli-Opitz_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome": 1,
    "Inborn_genetic_diseases|DHCR7-related_disorder|not_provided|Smith-Lemli-Opitz_syndrome|See_cases": 1,
    "not_specified|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome": 1,
    "not_provided|Smith-Lemli-Opitz_syndrome|See_cases|Inborn_genetic_diseases|DHCR7-related_disorder": 1,
    "Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|not_provided|DHCR7-related_disorder": 1,
    "DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome|not_provided": 4,
    "DHCR7-related_disorder|not_provided|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Smith-Lemli-Opitz_syndrome|not_provided": 2,
    "Smith-Lemli-Opitz_syndrome|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome|not_provided": 1,
    "Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "2-3_toe_syndactyly|Elevated_circulating_7-dehydrocholesterol_concentration|Primary_microcephaly|Small_for_gestational_age": 1,
    "Hepatoblastoma|Smith-Lemli-Opitz_syndrome": 1,
    "DHCR7-related_disorder|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|DHCR7-related_disorder|not_provided|Smith-Lemli-Opitz_syndrome": 2,
    "DHCR7-related_disorder|Inborn_genetic_diseases|not_provided|Smith-Lemli-Opitz_syndrome|2-3_toe_syndactyly|Elevated_circulating_7-dehydrocholesterol_concentration|Small_for_gestational_age|Primary_microcephaly": 1,
    "not_specified|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder": 1,
    "Smith-Lemli-Opitz_syndrome|not_provided|not_specified|Inborn_genetic_diseases|DHCR7-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome": 1,
    "Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Smith-Lemli-Opitz_syndrome|See_cases|Abnormal_brain_morphology": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Smith-Lemli-Opitz_syndrome": 1,
    "DHCR7-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Smith-Lemli-Opitz_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Smith-Lemli-Opitz_syndrome": 1,
    "not_provided|not_specified|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|DHCR7-related_disorder": 1,
    "Smith-Lemli-Opitz_syndrome|Microcephaly|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Smith-Lemli-Opitz_syndrome|DHCR7-related_disorder": 1,
    "DHCR7-related_disorder|Inborn_genetic_diseases|Smith-Lemli-Opitz_syndrome|not_provided": 1,
    "not_provided|Smith-Lemli-Opitz_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3": 11,
    "NADSYN1-related_disorder|not_provided": 3,
    "Congenital_NAD_deficiency_disorder|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3": 4,
    "NADSYN1-related_disorder": 7,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3|not_provided": 5,
    "not_provided|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3": 7,
    "Inborn_genetic_diseases|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3": 1,
    "NADSYN1-related_disorder|Congenital_NAD_deficiency_disorder|not_provided": 1,
    "NADSYN1-related_disorder|Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3": 2,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3|not_provided|NADSYN1-related_disorder|Congenital_NAD_deficiency_disorder|Neurodevelopmental_delay": 1,
    "Vertebral|_cardiac|_renal|_and_limb_defects_syndrome_3|NADSYN1-related_disorder": 1,
    "Hepatitis|_fulminant_viral|_susceptibility_to|not_provided": 1,
    "Hepatitis|_fulminant_viral|_susceptibility_to": 1,
    "NUMA1-related_disorder": 16,
    "NUMA1-related_disorder|not_provided": 3,
    "Acute_promyelocytic_leukemia|not_provided": 1,
    "not_provided|Acute_promyelocytic_leukemia": 1,
    "not_provided|NUMA1-related_disorder": 2,
    "not_specified|NUMA1-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_63": 74,
    "not_provided|LRTOMT-related_disorder": 3,
    "not_specified|LRTOMT-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_63|not_provided": 1,
    "LRTOMT-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "LRTOMT-related_disorder": 4,
    "LRTOMT-related_disorder|not_provided": 1,
    "not_specified|Hearing_loss|_autosomal_recessive|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_63|not_provided": 3,
    "LRTOMT-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 3,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 2,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_63|Inborn_genetic_diseases": 2,
    "LRTOMT-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_63|not_specified|not_provided": 1,
    "LRTOMT-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_63|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_63": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_63|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_63|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_63": 1,
    "FOLR3-related_disorder": 17,
    "FOLR3-related_disorder|not_provided": 1,
    "Cerebral_folate_transport_deficiency": 158,
    "Cerebral_folate_transport_deficiency|not_provided": 7,
    "not_provided|Cerebral_folate_transport_deficiency|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Cerebral_folate_transport_deficiency": 2,
    "not_provided|Cerebral_folate_transport_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Cerebral_folate_transport_deficiency": 3,
    "Inborn_genetic_diseases|Cerebral_folate_transport_deficiency": 8,
    "Cerebral_folate_transport_deficiency|Inborn_genetic_diseases": 5,
    "not_provided|Cerebral_folate_transport_deficiency": 8,
    "Inborn_genetic_diseases|not_provided|not_specified|Cerebral_folate_transport_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Cerebral_folate_transport_deficiency": 1,
    "Cerebral_folate_transport_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Cerebral_folate_transport_deficiency|not_specified": 4,
    "Cerebral_folate_transport_deficiency|FOLR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Cerebral_folate_transport_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|FOLR1-related_disorder|not_specified|not_provided|Cerebral_folate_transport_deficiency": 1,
    "FOLR1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Cerebral_folate_transport_deficiency": 1,
    "not_specified|Cerebral_folate_transport_deficiency|Inborn_genetic_diseases": 2,
    "Cerebral_folate_transport_deficiency|FOLR1-related_disorder": 1,
    "not_specified|not_provided|Cerebral_folate_transport_deficiency": 1,
    "FOLR1-related_disorder|Cerebral_folate_transport_deficiency": 2,
    "not_provided|not_specified|FOLR1-related_disorder|Cerebral_folate_transport_deficiency": 1,
    "FOLR1-related_disorder|Inborn_genetic_diseases|not_provided|Cerebral_folate_transport_deficiency|Seizure": 1,
    "Intellectual_disability|Cerebral_folate_transport_deficiency": 1,
    "not_provided|Cerebral_folate_transport_deficiency|Inborn_genetic_diseases|not_specified|FOLR1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Cerebral_folate_transport_deficiency": 1,
    "Opsismodysplasia": 31,
    "not_provided|Opsismodysplasia": 8,
    "not_provided|INPPL1-related_disorder": 8,
    "Opsismodysplasia|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|Opsismodysplasia": 1,
    "INPPL1-related_disorder": 5,
    "INPPL1-related_disorder|not_provided": 3,
    "not_provided|INPPL1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Opsismodysplasia": 1,
    "PHOX2A-related_disorder": 4,
    "PHOX2A-related_disorder|not_provided": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_2": 3,
    "3-methylglutaconic_aciduria|_type_VIIB": 472,
    "not_specified|3-methylglutaconic_aciduria|_type_VIIB|not_provided": 1,
    "CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB|not_provided": 3,
    "not_provided|3-methylglutaconic_aciduria|_type_VIIB": 27,
    "CLPB-related_disorder": 6,
    "3-methylglutaconic_aciduria|_type_VIIB|not_provided|Inborn_genetic_diseases": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|Inborn_genetic_diseases|CLPB-related_disorder": 1,
    "CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB": 6,
    "3-methylglutaconic_aciduria|_type_VIIB|Inborn_genetic_diseases": 17,
    "CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB|not_provided": 6,
    "3-methylglutaconic_aciduria|_type_VIIB|not_provided": 31,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB|not_specified|not_provided": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|not_specified": 7,
    "3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|CLPB-related_disorder": 3,
    "not_specified|3-methylglutaconic_aciduria|_type_VIIB": 6,
    "3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant|not_provided": 1,
    "3-methylglutaconic_aciduria|_type_VIIA|3-methylglutaconic_aciduria|_type_VIIB|not_provided": 1,
    "Neutropenia|_severe_congenital|_9|_autosomal_dominant": 4,
    "Microcytic_anemia|3-Methylglutaric_aciduria|3-Methylglutaconic_aciduria|Myeloid_maturation_arrest|not_provided|3-methylglutaconic_aciduria|_type_VIIB": 1,
    "Inborn_genetic_diseases|CLPB-related_disorder|not_specified|3-methylglutaconic_aciduria|_type_VIIB": 1,
    "not_provided|Neutropenia|_severe_congenital|_2|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIB": 1,
    "not_provided|Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB": 2,
    "3-methylglutaconic_aciduria|_type_VIIA": 3,
    "CLPB-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB|not_provided|CLPB-related_disorder": 1,
    "Decreased_total_neutrophil_count|Premature_ovarian_insufficiency": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIA|not_provided|Decreased_total_neutrophil_count|Premature_ovarian_insufficiency": 1,
    "Inborn_genetic_diseases|not_provided|3-methylglutaconic_aciduria|_type_VIIB": 4,
    "not_provided|CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB": 2,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIA|not_provided": 1,
    "not_provided|3-methylglutaconic_aciduria|_type_VIIB|not_specified": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|not_provided|not_specified": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|not_provided|CLPB-related_disorder": 1,
    "3-methylglutaconic_aciduria|_type_VIIA|Neutropenia|_severe_congenital|_9|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIB|Inborn_genetic_diseases|CLPB-related_disorder": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|not_specified|not_provided": 1,
    "CLPB-related_disorder|not_provided|3-methylglutaconic_aciduria|_type_VIIB|not_specified": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|not_specified|CLPB-related_disorder": 1,
    "3-methylglutaconic_aciduria|_type_VIIA|3-methylglutaconic_aciduria|_type_VIIB|Inborn_genetic_diseases": 1,
    "3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIA": 2,
    "3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIA|not_specified|not_provided": 1,
    "Neutropenia|_severe_congenital|_9|_autosomal_dominant|Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB|Neutropenia|_severe_congenital|_9|_autosomal_dominant|3-methylglutaconic_aciduria|_type_VIIA": 1,
    "CLPB-related_disorder|3-methylglutaconic_aciduria|_type_VIIB|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|3-methylglutaconic_aciduria|_type_VIIB|CLPB-related_disorder": 1,
    "not_provided|3-methylglutaconic_aciduria|_type_VIIB|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_paroxysmal_dyskinesia_or_seizures": 12,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_paroxysmal_dyskinesia_or_seizures": 2,
    "not_provided|Intellectual_developmental_disorder_with_paroxysmal_dyskinesia_or_seizures|Inborn_genetic_diseases": 1,
    "PDE2A-related_disorder": 2,
    "Intellectual_developmental_disorder_with_paroxysmal_dyskinesia_or_seizures|EEG_abnormality|Interictal_EEG_abnormality|Chorea|Paroxysmal_dystonia|Intellectual_disability|_moderate|Generalized_hypotonia": 1,
    "Intellectual_developmental_disorder_with_paroxysmal_dyskinesia_or_seizures|Inborn_genetic_diseases": 1,
    "Amelogenesis_imperfecta|_type_3C": 5,
    "not_provided|RELT-related_disorder": 3,
    "RELT-related_disorder": 8,
    "not_provided|Amelogenesis_imperfecta|_type_3C": 1,
    "DNAJB13-related_disorder": 1,
    "DNAJB13-related_disorder|not_provided": 4,
    "Primary_ciliary_dyskinesia_34": 5,
    "not_provided|DNAJB13-related_disorder": 2,
    "Primary_ciliary_dyskinesia_34|not_provided": 2,
    "DNAJB13-related_disorder|Primary_ciliary_dyskinesia_34|not_provided": 1,
    "Primary_ciliary_dyskinesia_34|not_provided|not_specified": 1,
    "Cough|not_provided": 1,
    "not_provided|DNAJB13-related_disorder|Primary_ciliary_dyskinesia_34": 1,
    "not_specified|not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_4": 2,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_4|not_specified": 1,
    "not_specified|not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_4|UCP2-related_disorder": 1,
    "UCP2-related_disorder|not_specified": 1,
    "UCP2-related_disorder": 1,
    "not_provided|UCP2-related_disorder|not_specified": 1,
    "not_specified|not_provided|UCP2-related_disorder": 1,
    "not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_4|not_specified": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_4": 1,
    "UCP3-related_disorder|not_specified": 11,
    "UCP3-related_disorder|not_specified|Obesity|not_provided": 1,
    "UCP3-related_disorder": 88,
    "UCP3-related_disorder|not_provided": 17,
    "not_provided|UCP3-related_disorder": 10,
    "not_specified|UCP3-related_disorder|not_provided": 1,
    "UCP3-related_disorder|UCP3_POLYMORPHISM|_EXON_6_SPLICE_DONOR_JUNCTION|Morbid_obesity|not_provided": 1,
    "not_specified|UCP3-related_disorder": 10,
    "UCP3-related_disorder|Obesity|not_specified": 1,
    "UCP3-related_disorder|not_provided|Inherited_obesity|Obesity|_severe|_and_type_II_diabetes": 1,
    "UCP3-related_disorder|not_specified|Obesity": 1,
    "not_provided|UCP3-related_disorder|not_specified": 2,
    "Obesity|not_provided": 4,
    "Obesity|UCP3-related_disorder|not_provided": 2,
    "Inherited_obesity|Short-rib_thoracic_dysplasia_13_with_or_without_polydactyly|not_provided|UCP3_POLYMORPHISM_G/A|Obesity|_severe|_and_type_II_diabetes": 1,
    "not_specified|UCP3-related_disorder|Obesity": 1,
    "not_specified|not_provided|UCP3-related_disorder": 1,
    "UCP3-related_disorder|Inherited_obesity|Obesity|_severe|_and_type_II_diabetes|not_provided": 1,
    "UCP3-related_disorder|not_provided|not_specified": 1,
    "Orofaciodigital_syndrome_type_14|not_provided": 9,
    "C2CD3-related_disorder|not_provided": 17,
    "not_provided|C2CD3-related_disorder": 15,
    "C2CD3-related_disorder": 7,
    "not_provided|Orofaciodigital_syndrome_type_14": 11,
    "Orofaciodigital_syndrome_type_14": 17,
    "Orofaciodigital_syndrome_type_14|not_provided|Inborn_genetic_diseases": 2,
    "Orofaciodigital_syndrome_type_14|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome|Jeune_thoracic_dystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Orofaciodigital_syndrome_type_14": 2,
    "not_provided|Orofaciodigital_syndrome_type_14|Inborn_genetic_diseases": 1,
    "Orofaciodigital_syndrome_type_14|not_provided|Rudimentary_fibula|Ankle_flexion_contracture": 1,
    "C2CD3-related_disorder|not_specified|not_provided": 1,
    "Orofaciodigital_syndrome_type_14|Inborn_genetic_diseases": 2,
    "C2CD3-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_provided": 1,
    "C2CD3-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Joubert_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|C2CD3-related_disorder": 1,
    "C2CD3-related_disorder|Inborn_genetic_diseases|Orofaciodigital_syndrome_type_14|not_specified|not_provided": 1,
    "Orofaciodigital_syndrome_type_14|Joubert_syndrome": 1,
    "Rudimentary_fibula|Ankle_flexion_contracture": 1,
    "PGM2L1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skin_abnormalities": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_dysmorphic_facies|_and_skin_abnormalities|not_provided": 3,
    "Brugada_syndrome_6": 19,
    "Long_QT_syndrome|Cardiovascular_phenotype|Brugada_syndrome_6|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_6|not_provided|Brugada_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_6": 15,
    "Brugada_syndrome_6|Cardiovascular_phenotype": 14,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_6": 1,
    "Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|Cardiovascular_phenotype|Periodic_paralysis|not_specified|not_provided|Cardiomyopathy|Brugada_syndrome_6|Ventricular_fibrillation|Syncope": 1,
    "Brugada_syndrome_6|Cardiovascular_phenotype|Prolonged_QT_interval": 1,
    "KCNE3-related_disorder|Brugada_syndrome_6|not_specified": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_6|not_provided": 1,
    "not_provided|Brugada_syndrome_6|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_6|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Brugada_syndrome_6|Cardiovascular_phenotype": 1,
    "Prolonged_QT_interval": 3,
    "Brugada_syndrome_6|not_provided": 2,
    "Brugada_syndrome_6|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_6": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Brugada_syndrome_6": 1,
    "not_specified|Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|not_provided|Brugada_syndrome_6|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_6|not_provided": 1,
    "not_specified|KCNE3-related_disorder": 1,
    "not_provided|Brugada_syndrome_6": 1,
    "not_provided|LIPT2-related_disorder|Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities": 2,
    "Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|LIPT2-related_disorder|not_provided": 1,
    "Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|not_provided": 2,
    "LIPT2-related_disorder": 1,
    "LIPT2-related_disorder|Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|not_provided": 1,
    "not_provided|Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|Early-onset_progressive_encephalopathy-hearing_loss-pons_hypoplasia-brain_atrophy_syndrome": 1,
    "Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities": 4,
    "not_provided|Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities": 2,
    "not_provided|LIPT2-related_disorder": 3,
    "Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|not_provided|not_specified": 1,
    "LIPT2-related_disorder|not_provided": 2,
    "Encephalopathy|_neonatal_severe|_with_lactic_acidosis_and_brain_abnormalities|LIPT2-related_disorder": 1,
    "Immunodeficiency_122": 2,
    "POLD3-related_disorder": 3,
    "POLD3-related_disorder|not_provided": 1,
    "Alkaline_phosphatase|_plasma_level_of|_quantitative_trait_locus_2|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta_type_10": 32,
    "Preterm_premature_rupture_of_membranes": 1,
    "not_provided|Osteogenesis_imperfecta_type_10": 13,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_10": 6,
    "SERPINH1-related_disorder|not_provided|Osteogenesis_imperfecta_type_10": 2,
    "Osteogenesis_imperfecta|not_specified|SERPINH1-related_disorder|not_provided": 1,
    "Osteogenesis_imperfecta_type_10|not_provided|not_specified": 1,
    "SERPINH1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_10": 1,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta_type_10": 2,
    "Osteogenesis_imperfecta_type_10|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_10": 1,
    "SERPINH1-related_disorder|Osteogenesis_imperfecta_type_10|Preterm_premature_rupture_of_membranes|not_specified|not_provided": 1,
    "Preterm_premature_rupture_of_membranes|Osteogenesis_imperfecta_type_10": 1,
    "Osteogenesis_imperfecta_type_10|Osteogenesis_imperfecta|not_provided|not_specified": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_10|Osteogenesis_imperfecta": 1,
    "not_provided|SERPINH1-related_disorder": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_10": 1,
    "Osteogenesis_imperfecta_type_10|Inborn_genetic_diseases": 2,
    "Osteogenesis_imperfecta_type_10|Osteogenesis_imperfecta|not_provided": 1,
    "WNT11-related_disorder": 1,
    "WNT11-related_disorder|Bladder_exstrophy-epispadias-cloacal_extrophy_complex": 1,
    "EMSY-related_disorder": 5,
    "Cleft_palate|_proliferative_retinopathy|_and_developmental_delay|Global_developmental_delay|Cleft_palate|Vitreoretinopathy": 1,
    "LRRC32-related_disorder": 4,
    "Cleft_palate|_proliferative_retinopathy|_and_developmental_delay": 2,
    "ACER3-related_disorder|not_provided": 5,
    "Alkaline_ceramidase_3_deficiency": 8,
    "not_provided|Alkaline_ceramidase_3_deficiency": 2,
    "ACER3-related_disorder": 1,
    "not_provided|CAPN5-related_disorder": 8,
    "Late-onset_cone-rod_dystrophy|Retinal_dystrophy|not_provided": 1,
    "CAPN5-related_disorder|not_provided": 10,
    "not_provided|Inborn_genetic_diseases|CAPN5-related_disorder": 1,
    "Autosomal_dominant_neovascular_inflammatory_vitreoretinopathy|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_neovascular_inflammatory_vitreoretinopathy|not_provided": 1,
    "Autosomal_dominant_neovascular_inflammatory_vitreoretinopathy|not_provided|Proliferative_vitreoretinopathy": 1,
    "Proliferative_vitreoretinopathy|not_provided": 1,
    "Proliferative_vitreoretinopathy": 2,
    "not_provided|Proliferative_vitreoretinopathy": 1,
    "not_specified|not_provided|CAPN5-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Proliferative_vitreoretinopathy|CAPN5-related_disorder": 1,
    "not_provided|Autosomal_dominant_neovascular_inflammatory_vitreoretinopathy": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_neovascular_inflammatory_vitreoretinopathy|High_myopia": 1,
    "Inborn_genetic_diseases|CAPN5-related_disorder|not_provided": 2,
    "Severe_early-childhood-onset_retinal_dystrophy|Inborn_genetic_diseases": 1,
    "CAPN5-related_disorder": 1,
    "not_provided|not_specified|Proliferative_vitreoretinopathy": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 11,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 18,
    "Nonsyndromic_Hearing_Loss|_Dominant|Retinitis_pigmentosa-deafness_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Usher_syndrome_type_1B": 114,
    "Usher_syndrome_type_1|Rare_genetic_deafness|Usher_syndrome|not_provided": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Meniere_disease|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B": 146,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 14,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 3,
    "MYO7A-related_disorder|not_provided": 22,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 45,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Rare_genetic_deafness|not_provided": 1,
    "not_provided|Usher_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Hearing_loss|_autosomal_recessive|Usher_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Intellectual_disability": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B|not_provided": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1B": 2,
    "Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1|not_provided": 4,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|not_provided": 88,
    "not_specified|Usher_syndrome_type_1B|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2": 79,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 17,
    "not_provided|Rare_genetic_deafness|Usher_syndrome|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|Retinitis_pigmentosa|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1|Retinal_dystrophy|not_provided|Rare_genetic_deafness": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided": 12,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|MYO7A-related_disorder": 13,
    "MYO7A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 14,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Cone-rod_dystrophy|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 11,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|not_specified|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 3,
    "MYO7A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided|not_specified": 1,
    "MYO7A-related_disorder|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Deafness|Hearing_loss|_autosomal_recessive|Rare_genetic_deafness": 1,
    "not_provided|Monogenic_hearing_loss": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 6,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 9,
    "Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_specified|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 10,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1B": 11,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Inborn_genetic_diseases|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|not_specified|not_provided": 1,
    "MYO7A-related_disorder|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 10,
    "Usher_syndrome|MYO7A-related_disorder|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided": 20,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome|Usher_syndrome_type_1B|not_specified|not_provided": 1,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness": 1,
    "Usher_syndrome|MYO7A-related_disorder|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Rare_genetic_deafness|not_provided": 1,
    "not_provided|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_specified|Usher_syndrome_type_1B|not_provided": 4,
    "Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "Usher_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 9,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|Usher_syndrome|Retinal_dystrophy|not_provided": 1,
    "MYO7A-related_disorder|Rare_genetic_deafness|Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|MYO7A-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|not_specified|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|not_provided|MYO7A-related_disorder": 5,
    "Retinitis_pigmentosa|Usher_syndrome_type_1B": 1,
    "MYO7A-related_disorder|Usher_syndrome_type_1B|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|not_specified": 1,
    "not_specified|Usher_syndrome_type_1B": 10,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|not_specified|Hearing_impairment": 1,
    "Usher_syndrome_type_1B|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 6,
    "not_provided|Usher_syndrome_type_1B|Retinal_dystrophy|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11": 16,
    "not_specified|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 5,
    "MYO7A-related_disorder": 14,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome|Retinal_dystrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Retinal_dystrophy|Rare_genetic_deafness|not_provided|Usher_syndrome|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|not_provided": 3,
    "Usher_syndrome_type_1B|not_provided|not_specified": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness|Retinal_dystrophy|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|See_cases": 1,
    "Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|not_specified|Usher_syndrome_type_1": 1,
    "not_provided|not_specified|Bilateral_sensorineural_hearing_impairment|MYO7A-related_disorder|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness|not_provided|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|Inborn_genetic_diseases|Hearing_loss|_autosomal_recessive|Retinal_dystrophy|not_provided|Usher_syndrome": 1,
    "not_specified|not_provided|Usher_syndrome_type_1B": 5,
    "Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1B": 5,
    "Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 2,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided": 1,
    "MYO7A-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 7,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 5,
    "not_specified|MYO7A-related_disorder|not_provided": 1,
    "Usher_syndrome|Retinal_dystrophy|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Rare_genetic_deafness|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness|Usher_syndrome_type_1B|Retinal_dystrophy|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Retinal_dystrophy|Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided|Usher_syndrome|not_specified|Meniere_disease|MYO7A-related_disorder": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 11,
    "Usher_syndrome_type_1B|not_provided|Inborn_genetic_diseases": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "MYO7A-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "Retinal_dystrophy|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_provided|MYO7A-related_disorder|Inborn_genetic_diseases|Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "MYO7A-related_disorder|not_provided|Retinal_dystrophy|not_specified|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified": 2,
    "Usher_syndrome_type_1B|Retinal_dystrophy": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 8,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Nonsyndromic_genetic_hearing_loss|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_provided|not_specified|Usher_syndrome_type_1B": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Rare_genetic_deafness|not_provided": 2,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome|not_provided": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Hearing_loss|_autosomal_recessive|Rare_genetic_deafness|not_provided": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Retinal_dystrophy|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 2,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1": 1,
    "MYO7A-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Usher_syndrome_type_1|not_provided": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Nonsyndromic_genetic_hearing_loss|not_provided|Usher_syndrome_type_1B|Ear_malformation": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Nonsyndromic_genetic_hearing_loss|Usher_syndrome_type_1|Usher_syndrome_type_1B|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 7,
    "Usher_syndrome|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "MYO7A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified": 4,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_2|MYO7A-related_disorder|not_provided": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1|MYO7A-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|not_specified": 3,
    "Rare_genetic_deafness|Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Retinal_dystrophy|not_provided|Hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "Usher_syndrome|Usher_syndrome_type_1": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided": 1,
    "Usher_syndrome_type_1B|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1B|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Retinal_dystrophy": 1,
    "not_provided|Usher_syndrome_type_1B|not_specified": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Usher_syndrome_type_1B|Inborn_genetic_diseases": 10,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome": 1,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|not_specified": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Ear_malformation": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hearing_impairment": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_provided|not_specified|MYO7A-related_disorder": 2,
    "Usher_syndrome_type_1|Usher_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 4,
    "not_specified|Usher_syndrome_type_1|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "not_provided|not_specified|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Nonsyndromic_genetic_hearing_loss|not_specified": 1,
    "Usher_syndrome_type_1|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_provided|Usher_syndrome_type_1B|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|MYO7A-related_disorder|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Nonsyndromic_genetic_hearing_loss|Usher_syndrome_type_1|Hearing_loss|_autosomal_recessive|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 2,
    "MYO7A-related_disorder|not_provided|Usher_syndrome_type_1B": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_provided": 1,
    "Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness|Usher_syndrome_type_1B|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_specified|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|not_specified": 1,
    "not_specified|Usher_syndrome_type_1|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1": 4,
    "Rare_genetic_deafness|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B|Usher_syndrome": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Rare_genetic_deafness|not_provided|Usher_syndrome|MYO7A-related_disorder|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_specified|not_provided|Usher_syndrome_type_1B|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "not_specified|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|Meniere_disease|MYO7A-related_disorder": 1,
    "MYO7A-related_disorder|not_specified|not_provided": 3,
    "Usher_syndrome_type_1B|not_specified|not_provided|MYO7A-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|MYO7A-related_disorder|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1B": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "not_provided|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "MYO7A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Hearing_impairment": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 1,
    "not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Hearing_loss|_autosomal_recessive": 3,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Inborn_genetic_diseases|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1": 14,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Inborn_genetic_diseases|Usher_syndrome_type_1B|Nonsyndromic_genetic_hearing_loss": 1,
    "Usher_syndrome_type_1B|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "MYO7A-related_disorder|not_specified": 1,
    "MYO7A-related_disorder|Inborn_genetic_diseases|Usher_syndrome_type_1B|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Usher_syndrome_type_1|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|MYO7A-related_disorder|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Inborn_genetic_diseases": 1,
    "MYO7A-related_disorder|Usher_syndrome|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B": 2,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|not_provided": 1,
    "not_provided|not_specified|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Meniere_disease|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|MYO7A-related_disorder|not_provided": 1,
    "not_provided|MYO7A-related_disorder|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Inborn_genetic_diseases|not_specified|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome|Usher_syndrome_type_1": 1,
    "MYO7A-related_disorder|Inborn_genetic_diseases|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1B|not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|not_specified|Meniere_disease|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|MYO7A-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1B|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Hearing_impairment": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|MYO7A-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 2,
    "Hearing_loss|_autosomal_recessive|Retinitis_pigmentosa-deafness_syndrome|not_provided|Nonsyndromic_Hearing_Loss|_Dominant": 2,
    "not_specified|not_provided|Usher_syndrome_type_1B|MYO7A-related_disorder|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 2,
    "MYO7A-related_disorder|not_provided|not_specified|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Hearing_impairment": 1,
    "Usher_syndrome_type_1B|not_provided|MYO7A-related_disorder|not_specified": 2,
    "Optic_atrophy|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Cone-rod_dystrophy|Hearing_impairment|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Rare_genetic_deafness|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B|Retinal_dystrophy|Rare_genetic_deafness|not_provided": 1,
    "Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|MYO7A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Retinal_dystrophy|Hearing_impairment|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Inborn_genetic_diseases|MYO7A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|MYO7A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Retinal_dystrophy": 1,
    "not_provided|MYO7A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Usher_syndrome_type_1B": 2,
    "Usher_syndrome_type_1B|not_specified|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Retinitis_pigmentosa|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Pendred_syndrome": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Deafness|Hearing_loss|_autosomal_recessive|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 2,
    "not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Inborn_genetic_diseases": 1,
    "MYO7A-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B|Rare_genetic_deafness|Hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|MYO7A-related_disorder|Retinal_dystrophy|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|MYO7A-related_disorder|Usher_syndrome_type_1|Usher_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|MYO7A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Hearing_loss|_autosomal_recessive": 1,
    "MYO7A-related_disorder|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "not_provided|MYO7A-related_disorder|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|MYO7A-related_disorder|Rare_genetic_deafness|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1B": 1,
    "not_provided|Usher_syndrome_type_1B|not_specified|Usher_syndrome_type_1|MYO7A-related_disorder": 1,
    "Usher_syndrome|Retinal_dystrophy|not_provided|Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder": 1,
    "not_specified|MYO7A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Retinal_dystrophy|Rare_genetic_deafness": 1,
    "Usher_syndrome|not_provided|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|MYO7A-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "not_specified|not_provided|MYO7A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1": 1,
    "Usher_syndrome|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Retinal_dystrophy|not_provided|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "MYO7A-related_disorder|Usher_syndrome_type_1|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Ear_malformation|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome|not_provided": 1,
    "MYO7A-related_disorder|Usher_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Retinal_dystrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome|not_provided|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified": 1,
    "Usher_syndrome_type_1B|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 4,
    "Rare_genetic_deafness|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Hypoglycemia|Global_developmental_delay|Hepatomegaly|Seizure|Sensorineural_hearing_loss_disorder|Usher_syndrome_type_1B": 1,
    "not_specified|not_provided|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|MYO7A-related_disorder|Usher_syndrome_type_1B|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome|Retinal_dystrophy|Nonsyndromic_genetic_hearing_loss|not_provided|Usher_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1B": 1,
    "Usher_syndrome|Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|MYO7A-related_disorder|not_provided": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B|not_provided": 1,
    "not_provided|Usher_syndrome_type_1B|MYO7A-related_disorder": 1,
    "Usher_syndrome_type_1B|not_specified|not_provided": 2,
    "Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder|Usher_syndrome_type_1|not_provided": 1,
    "Usher_syndrome|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_specified|not_provided|MYO7A-related_disorder": 1,
    "Usher_syndrome_type_1B|Inborn_genetic_diseases|not_specified": 1,
    "Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|not_provided": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1B|not_provided|not_specified": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Cohen_syndrome": 1,
    "not_provided|Usher_syndrome_type_1|Usher_syndrome|Retinal_dystrophy": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome|not_provided|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1B|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 2,
    "not_provided|MYO7A-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided": 1,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1B|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Usher_syndrome_type_1|Retinal_dystrophy": 1,
    "MYO7A-related_disorder|not_provided|not_specified": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1B|Rare_genetic_deafness": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "MYO7A-related_disorder|not_provided|not_specified|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Rare_genetic_deafness": 1,
    "Retinal_dystrophy|not_provided|Usher_syndrome_type_1B|not_specified": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Usher_syndrome_type_1B|Deafness|not_specified|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Retinal_dystrophy|Usher_syndrome_type_1": 1,
    "not_provided|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|Usher_syndrome_type_1|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder|Usher_syndrome_type_1": 1,
    "MYO7A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder": 1,
    "Usher_syndrome_type_1B|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1B|not_provided": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Inborn_genetic_diseases|MYO7A-related_disorder|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Hearing_impairment|Retinal_dystrophy|Usher_syndrome_type_1|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1B|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|MYO7A-related_disorder|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 2,
    "Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1B": 3,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome|Rare_genetic_deafness|Usher_syndrome_type_1B|not_provided": 1,
    "Microcephaly|Global_developmental_delay|Short_stature|Sensorineural_hearing_loss_disorder": 1,
    "Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Usher_syndrome|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Inborn_genetic_diseases|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided|Usher_syndrome_type_1B": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1B|Retinitis_pigmentosa-deafness_syndrome|Nonsyndromic_Hearing_Loss|_Dominant|not_specified": 1,
    "Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome|not_provided": 2,
    "Retinal_dystrophy|not_specified|Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1B|not_specified|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_provided|Usher_syndrome_type_1B|MYO7A-related_disorder|not_specified": 1,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|not_specified|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Retinal_dystrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "MYO7A-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|Usher_syndrome_type_1|Usher_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Retinal_dystrophy|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1|not_specified|MYO7A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Retinal_dystrophy|not_provided|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided": 1,
    "Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Ear_malformation|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "MYO7A-related_disorder|not_specified|not_provided|Usher_syndrome_type_1B": 2,
    "MYO7A-related_disorder|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "MYO7A-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|Hearing_loss|_autosomal_dominant_80|not_provided": 1,
    "not_specified|Usher_syndrome_type_1B|not_provided|MYO7A-related_disorder": 1,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 2,
    "not_specified|Hearing_loss|_autosomal_recessive|not_provided|Deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1B|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_provided|MYO7A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Rare_genetic_deafness|Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|MYO7A-related_disorder|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|MYO7A-related_disorder|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|not_specified": 1,
    "Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|not_specified": 1,
    "not_provided|MYO7A-related_disorder|Rare_genetic_deafness|Usher_syndrome_type_1B|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|MYO7A-related_disorder|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Inborn_genetic_diseases|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Rare_genetic_deafness|Usher_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|MYO7A-related_disorder|not_provided|Usher_syndrome_type_1": 1,
    "not_provided|not_specified|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1": 1,
    "not_provided|Usher_syndrome_type_1B|Usher_syndrome": 1,
    "MYO7A-related_disorder|Usher_syndrome|Rare_genetic_deafness|Retinal_dystrophy|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|not_specified": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B|Retinal_dystrophy|not_provided": 1,
    "Rare_genetic_deafness|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome|not_provided": 1,
    "Usher_syndrome_type_1B|not_specified|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome|MYO7A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Monogenic_hearing_loss|Rare_genetic_deafness|MYO7A-related_disorder|Retinal_dystrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_provided|not_specified|Usher_syndrome_type_1": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Retinitis_pigmentosa|Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1B|Retinal_dystrophy|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Rare_genetic_deafness|MYO7A-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hearing_impairment|MYO7A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|not_specified|Usher_syndrome_type_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Inborn_genetic_diseases|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|MYO7A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1B|not_provided|Retinal_dystrophy": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_11|MYO7A-related_disorder": 1,
    "Rare_genetic_deafness|Retinal_dystrophy|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Rare_genetic_deafness|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1B|not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B|Usher_syndrome_type_1|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Retinal_dystrophy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "not_specified|Usher_syndrome_type_1B|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B|MYO7A-related_disorder|not_provided|not_specified": 1,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_1": 1,
    "Usher_syndrome_type_1B|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|not_provided|Usher_syndrome_type_1B": 1,
    "not_provided|not_specified|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Inborn_genetic_diseases|Meniere_disease|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Hearing_impairment": 1,
    "not_specified|MYO7A-related_disorder|Usher_syndrome_type_1B|not_provided": 1,
    "not_provided|Usher_syndrome|Rare_genetic_deafness": 1,
    "not_provided|Inborn_genetic_diseases|Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|MYO7A-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1|not_provided": 1,
    "not_provided|Retinal_dystrophy|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Usher_syndrome_type_1B|Autosomal_dominant_nonsyndromic_hearing_loss_11|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2|not_specified|Usher_syndrome_type_1B": 1,
    "Retinal_dystrophy|MYO7A-related_disorder|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome|Retinal_dystrophy": 1,
    "not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1B": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B|not_specified": 1,
    "Usher_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Usher_syndrome_type_1|not_provided|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_specified": 1,
    "Usher_syndrome_type_1|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_2|Autosomal_dominant_nonsyndromic_hearing_loss_11|not_provided": 1,
    "Usher_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_2|Usher_syndrome_type_1|Usher_syndrome_type_1B": 1,
    "Usher_syndrome_type_1B|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B": 1,
    "Meniere_disease|not_provided|Usher_syndrome_type_1B": 1,
    "Meniere_disease|not_specified|not_provided|Usher_syndrome_type_1|Autosomal_dominant_nonsyndromic_hearing_loss_11|Usher_syndrome_type_1B|Autosomal_recessive_nonsyndromic_hearing_loss_2": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|Nonsyndromic_Hearing_Loss|_Dominant|Retinitis_pigmentosa-deafness_syndrome": 1,
    "Intellectual_developmental_disorder_with_macrocephaly|_seizures|_and_speech_delay": 24,
    "PAK1-related_disorder": 5,
    "not_provided|See_cases|Intellectual_developmental_disorder_with_macrocephaly|_seizures|_and_speech_delay": 1,
    "Intellectual_developmental_disorder_with_macrocephaly|_seizures|_and_speech_delay|not_provided": 4,
    "not_specified|PAK1-related_disorder|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder_with_macrocephaly|_seizures|_and_speech_delay|PAK1-related_disorder": 1,
    "not_provided|Intellectual_developmental_disorder_with_macrocephaly|_seizures|_and_speech_delay": 2,
    "not_provided|PAK1-related_disorder": 4,
    "PAK1-related_disorder|not_provided": 1,
    "PAK1-related_disorder|PAK1-related_neurodevelopmental_disorders|not_provided": 1,
    "Mitochondrial_disease|Mitochondrial_complex_I_deficiency|_nuclear_type_36": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_36|Mitochondrial_disease": 1,
    "not_specified|not_provided|Congenital_disorder_of_glycosylation|ALG8_congenital_disorder_of_glycosylation": 1,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts|not_provided": 6,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts": 67,
    "ALG8_congenital_disorder_of_glycosylation": 114,
    "ALG8_congenital_disorder_of_glycosylation|ALG8-related_disorder": 7,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts|not_provided|ALG8-related_disorder": 1,
    "Polycystic_liver_disease_3_with_or_without_kidney_cysts": 6,
    "ALG8-related_disorder": 7,
    "Inborn_genetic_diseases|ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts": 5,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts|Inborn_genetic_diseases": 7,
    "ALG8-related_disorder|ALG8_congenital_disorder_of_glycosylation": 5,
    "Inborn_genetic_diseases|ALG8_congenital_disorder_of_glycosylation": 3,
    "not_specified|not_provided|ALG8_congenital_disorder_of_glycosylation": 4,
    "ALG8-related_disorder|ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts": 3,
    "Inborn_genetic_diseases|ALG8_congenital_disorder_of_glycosylation|not_specified": 1,
    "ALG8-related_disorder|ALG8_congenital_disorder_of_glycosylation|not_provided": 2,
    "Inborn_genetic_diseases|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation": 1,
    "not_provided|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation": 2,
    "ALG8_congenital_disorder_of_glycosylation|not_provided|Polycystic_liver_disease_3_with_or_without_kidney_cysts|Inborn_genetic_diseases": 1,
    "Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation|Familial_cystic_renal_disease": 1,
    "Inborn_genetic_diseases|Familial_cystic_renal_disease|not_provided|ALG8-related_disorder|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation|Autosomal_dominant_polycystic_liver_disease|See_cases": 1,
    "not_provided|ALG8_congenital_disorder_of_glycosylation|not_specified": 1,
    "Polycystic_liver_disease_3_with_or_without_kidney_cysts|Familial_cystic_renal_disease": 1,
    "ALG8_congenital_disorder_of_glycosylation|Familial_cystic_renal_disease|ALG8-related_disorder|Polycystic_liver_disease_3_with_or_without_kidney_cysts|Autosomal_dominant_polycystic_liver_disease": 1,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8-related_disorder|not_provided": 1,
    "ALG8_congenital_disorder_of_glycosylation|not_provided": 6,
    "ALG8_congenital_disorder_of_glycosylation|ALG8-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|ALG8_congenital_disorder_of_glycosylation": 7,
    "ALG8-related_disorder|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation|not_provided": 1,
    "Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation": 4,
    "ALG8_congenital_disorder_of_glycosylation|ALG8-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_polycystic_liver_disease|not_provided|ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts": 1,
    "ALG8-related_disorder|not_provided|ALG8_congenital_disorder_of_glycosylation": 3,
    "Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation|ALG8-related_disorder": 1,
    "ALG8_congenital_disorder_of_glycosylation|ALG8-related_disorder|not_provided|Polycystic_liver_disease_3_with_or_without_kidney_cysts|Familial_cystic_renal_disease": 1,
    "ALG8_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 2,
    "not_specified|ALG8_congenital_disorder_of_glycosylation|not_provided": 1,
    "Autosomal_dominant_polycystic_liver_disease|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts": 1,
    "ALG8_congenital_disorder_of_glycosylation|ALG8-related_disorder|not_specified|not_provided": 1,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts|Autosomal_dominant_polycystic_liver_disease": 1,
    "ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8-related_disorder": 1,
    "not_provided|ALG8_congenital_disorder_of_glycosylation|Polycystic_liver_disease_3_with_or_without_kidney_cysts": 2,
    "Familial_cystic_renal_disease|Polycystic_liver_disease_3_with_or_without_kidney_cysts|ALG8_congenital_disorder_of_glycosylation|not_provided": 1,
    "ALG8-related_disorder|not_provided": 1,
    "ALG8_congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_provided|Congenital_disorder_of_glycosylation|ALG8_congenital_disorder_of_glycosylation": 1,
    "NARS2-related_primary_mitochondrial_disorder": 1,
    "NARS2-related_disorder": 4,
    "Combined_oxidative_phosphorylation_defect_type_24|NARS2-related_disorder|not_provided": 3,
    "Intellectual_disability|not_specified|NARS2-related_disorder|not_provided": 1,
    "not_provided|NARS2-related_disorder|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_defect_type_24|not_provided|not_specified": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_24": 4,
    "Combined_oxidative_phosphorylation_defect_type_24|not_provided": 7,
    "Inborn_genetic_diseases|not_provided|NARS2-related_disorder": 1,
    "NARS2-related_disorder|not_specified|not_provided": 2,
    "Acute_refractory_chorea": 1,
    "NARS2-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_24": 1,
    "Hearing_loss|_autosomal_recessive_94|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_recessive_94": 1,
    "NARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_24|Hearing_loss|_autosomal_recessive_94|not_provided|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_recessive_94": 1,
    "Combined_oxidative_phosphorylation_defect_type_24|Hearing_loss|_autosomal_recessive_94": 2,
    "Hearing_loss|_autosomal_recessive_94|Combined_oxidative_phosphorylation_defect_type_24|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_24|not_provided": 2,
    "not_provided|not_specified|Hearing_loss|_autosomal_recessive_94|Combined_oxidative_phosphorylation_defect_type_24": 1,
    "not_specified|Hearing_loss|_autosomal_recessive_94|not_provided|Combined_oxidative_phosphorylation_defect_type_24": 1,
    "Hearing_loss|_autosomal_recessive_94|Combined_oxidative_phosphorylation_defect_type_24|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|NARS2-related_disorder": 1,
    "TENM4-related_disorder": 32,
    "TENM4-related_disorder|not_provided": 8,
    "not_provided|TENM4-related_disorder": 12,
    "Tremor|_hereditary_essential|_5": 19,
    "not_specified|TENM4-related_disorder": 3,
    "Tremor|_hereditary_essential|_5|not_provided": 2,
    "not_provided|Tremor|_hereditary_essential|_5": 4,
    "TENM4-related_disorder|not_specified": 4,
    "Tremor|_hereditary_essential|_5|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Tremor|_hereditary_essential|_5|TENM4-related_disorder": 1,
    "not_provided|not_specified|Tremor|_hereditary_essential|_5": 1,
    "not_provided|TENM4-related_disorder|not_specified": 1,
    "TENM4-related_disorder|not_specified|not_provided": 2,
    "not_specified|TENM4-related_disorder|not_provided": 1,
    "not_specified|Tremor|_hereditary_essential|_5": 1,
    "Tremor|_hereditary_essential|_5|not_specified": 2,
    "TENM4-related_disorder|not_provided|Tremor|_hereditary_essential|_5": 1,
    "Tremor|_hereditary_essential|_5|not_specified|not_provided": 1,
    "not_specified|not_provided|TENM4-related_disorder": 1,
    "DLG2-related_disorder": 7,
    "not_provided|TMEM126B-related_disorder": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_29|not_provided": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_29|TMEM126B-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_29|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_29|Mitochondrial_disease": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_29": 1,
    "TMEM126B-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_29|Mitochondrial_complex_I_deficiency|not_provided|Mitochondrial_disease": 1,
    "TMEM126B-related_disorder": 1,
    "Optic_Atrophy|_Recessive": 2,
    "Autosomal_recessive_optic_atrophy|_OPA7_type": 5,
    "Autosomal_recessive_optic_atrophy|_OPA7_type|not_provided": 3,
    "not_specified|not_provided|Optic_Atrophy|_Recessive": 1,
    "not_specified|not_provided|Autosomal_recessive_optic_atrophy|_OPA7_type": 2,
    "not_provided|Autosomal_recessive_optic_atrophy|_OPA7_type": 3,
    "TMEM126A-related_disorder|not_specified|not_provided|Autosomal_recessive_optic_atrophy|_OPA7_type": 2,
    "not_specified|Autosomal_recessive_optic_atrophy|_OPA7_type|TMEM126A-related_disorder|not_provided": 1,
    "Autosomal_recessive_optic_atrophy|_OPA7_type|not_provided|TMEM126A-related_disorder": 1,
    "Autosomal_recessive_optic_atrophy|_OPA7_type|not_provided|not_specified": 1,
    "not_specified|Autosomal_recessive_optic_atrophy|_OPA7_type": 1,
    "not_provided|Autosomal_recessive_optic_atrophy|_OPA7_type|not_specified": 2,
    "TMEM126A-related_disorder|not_provided": 1,
    "not_specified|PICALM-related_disorder": 1,
    "not_specified|PICALM-related_disorder|not_provided": 1,
    "not_provided|PICALM-related_disorder": 1,
    "PICALM-related_disorder": 2,
    "not_provided|PICALM-related_disorder|not_specified": 1,
    "Cohen-Gibson_syndrome": 47,
    "Cohen-Gibson_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Cohen-Gibson_syndrome": 2,
    "Cohen-Gibson_syndrome|not_provided": 5,
    "Cohen-Gibson_syndrome|EED-related_disorder": 3,
    "EED-related_disorder|Inborn_genetic_diseases|Cohen-Gibson_syndrome": 1,
    "EED-related_disorder": 3,
    "not_provided|Cohen-Gibson_syndrome|EED-related_disorder": 1,
    "EED-related_disorder|Cohen-Gibson_syndrome": 2,
    "EED-related_disorder|not_provided|Cohen-Gibson_syndrome": 1,
    "not_provided|Hypomyelinating_leukodystrophy_13|HIKESHI-related_disorder": 1,
    "Hypomyelinating_leukodystrophy_13": 3,
    "FZD4-related_disorder": 2,
    "not_provided|FZD4-related_disorder": 2,
    "not_specified|Exudative_vitreoretinopathy_1|not_provided": 1,
    "Exudative_vitreoretinopathy_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Exudative_vitreoretinopathy_1|Inborn_genetic_diseases": 2,
    "Exudative_vitreoretinopathy_1|Inborn_genetic_diseases": 1,
    "FZD4-related_disorder|not_provided": 2,
    "Exudative_vitreoretinopathy_1|Familial_exudative_vitreoretinopathy|Exudative_retinopathy|Retinal_dystrophy|not_provided": 1,
    "Exudative_vitreoretinopathy|_digenic|Exudative_vitreoretinopathy_1": 1,
    "Inborn_genetic_diseases|not_provided|FZD4-related_disorder": 1,
    "Retinopathy_of_prematurity|not_provided|FZD4-related_disorder": 1,
    "not_provided|Exudative_vitreoretinopathy_1|not_specified": 1,
    "Exudative_vitreoretinopathy_1|Retinal_dystrophy|not_provided": 1,
    "not_provided|Exudative_retinopathy|Familial_exudative_vitreoretinopathy|FZD4-related_disorder|Atrophia_bulborum_hereditaria|Exudative_vitreoretinopathy_1|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Exudative_vitreoretinopathy_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Exudative_vitreoretinopathy_1": 1,
    "TMEM135-related_disorder": 7,
    "not_provided|TMEM135-related_disorder": 1,
    "Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome": 11,
    "CTSC-related_disorder|Haim-Munk_syndrome|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome": 1,
    "Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome": 109,
    "Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|not_specified|not_provided|Periodontitis|_aggressive_1": 1,
    "Haim-Munk_syndrome|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome": 57,
    "Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|Haim-Munk_syndrome|not_provided": 1,
    "Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|Periodontitis|_aggressive_1": 47,
    "Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1": 25,
    "Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome": 110,
    "Haim-Munk_syndrome|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome": 1,
    "Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|Periodontitis|_aggressive_1|not_provided": 1,
    "Papillon-Lef\u00e8vre_syndrome": 14,
    "Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|Haim-Munk_syndrome": 22,
    "Periodontitis|_aggressive_1": 1,
    "Haim-Munk_syndrome|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|not_provided": 4,
    "not_provided|not_specified|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1": 1,
    "not_provided|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome": 1,
    "Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome": 6,
    "CTSC-related_disorder": 4,
    "Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|See_cases": 1,
    "See_cases|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome": 1,
    "CTSC-related_disorder|Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome": 2,
    "Inborn_genetic_diseases|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome": 2,
    "not_provided|Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome": 1,
    "Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|not_provided": 1,
    "not_specified|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome": 1,
    "Inborn_genetic_diseases|Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome": 2,
    "Inborn_genetic_diseases|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|Periodontitis|_aggressive_1": 1,
    "not_provided|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|Haim-Munk_syndrome": 1,
    "Haim-Munk_syndrome": 1,
    "Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1": 1,
    "Inborn_genetic_diseases|Haim-Munk_syndrome|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome": 3,
    "Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|not_specified": 1,
    "Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|not_provided|not_specified": 2,
    "Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|not_provided": 1,
    "Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|not_specified": 1,
    "Haim-Munk_syndrome|Periodontitis|_aggressive_1|Papillon-Lef\u00e8vre_syndrome|CTSC-related_disorder": 1,
    "Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|not_provided|not_specified": 1,
    "Periodontitis|_aggressive_1|Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|CTSC-related_disorder": 1,
    "Haim-Munk_syndrome|Papillon-Lef\u00e8vre_syndrome|Periodontitis|_aggressive_1|Inborn_genetic_diseases": 1,
    "CTSC-related_disorder|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|Periodontitis|_aggressive_1": 1,
    "not_provided|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|not_specified": 1,
    "Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|not_provided": 3,
    "CTSC-related_disorder|Papillon-Lef\u00e8vre_syndrome|Haim-Munk_syndrome|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_1A": 16,
    "Myopia|Nystagmus|Albinism|Foveal_hypoplasia|Elevated_circulating_hepatic_transaminase_concentration|Slow_decrease_in_visual_acuity|Choroidal_neovascularization|Abnormality_of_metabolism/homeostasis|TYR-related_disorder|Albinism_or_congenital_nystagmus|Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Ocular_albinism_with_congenital_sensorineural_hearing_loss|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|not_provided|Hypopigmentation_of_the_skin|Hypopigmentation_of_hair|Iris_transillumination_defect|Horizontal_nystagmus|Abnormality_of_the_skin": 1,
    "Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A": 12,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 11,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B": 6,
    "Oculocutaneous_albinism_type_1": 6,
    "not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 5,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|not_provided": 9,
    "Albinism_or_congenital_nystagmus": 4,
    "Oculocutaneous_albinism|not_provided": 12,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 9,
    "Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|not_provided|TYR-related_disorder": 1,
    "not_provided|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Ocular_albinism": 1,
    "Oculocutaneous_albinism_type_1B": 7,
    "not_provided|not_specified|Oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1|not_provided|Oculocutaneous_albinism_type_1A": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided": 11,
    "not_provided|TYR-related_disorder": 8,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism": 1,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|Inborn_genetic_diseases|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_provided": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B": 6,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided": 6,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|not_provided|Nonsyndromic_Oculocutaneous_Albinism": 1,
    "not_specified|not_provided|Oculocutaneous_albinism": 1,
    "not_provided|Oculocutaneous_albinism": 6,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B": 4,
    "not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|TYR-related_disorder|not_provided|Oculocutaneous_albinism_type_1B": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|TYR-related_disorder|Albinism_or_congenital_nystagmus|Oculocutaneous_albinism|not_provided|See_cases": 1,
    "TYR-related_disorder|not_provided|not_specified": 1,
    "Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|not_provided": 3,
    "TYR-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism|Inborn_genetic_diseases|Oculocutaneous_albinism_type_1|Albinism|not_provided": 1,
    "Hypopigmentation_of_the_skin|Abnormal_retinal_morphology|Ocular_albinism|Fair_hair|Albinism|Strabismus|Abnormal_optic_nerve_morphology|Horizontal_nystagmus|not_provided|Oculocutaneous_albinism_type_1|Oculocutaneous_albinism_type_1A": 1,
    "not_provided|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 2,
    "Oculocutaneous_albinism_type_1|Oculocutaneous_albinism": 1,
    "TYR-related_disorder": 5,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Abnormality_of_the_skin": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided|Oculocutaneous_albinism": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Foveal_hypoplasia|Albinism|Slow_decrease_in_visual_acuity|Choroidal_neovascularization|Elevated_circulating_hepatic_transaminase_concentration|Abnormality_of_metabolism/homeostasis|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|not_provided|Oculocutaneous_albinism": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|TYR-related_disorder|not_provided|Ocular_albinism_with_congenital_sensorineural_hearing_loss": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Inborn_genetic_diseases|not_provided": 1,
    "TYR-related_disorder|not_provided": 3,
    "Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "Oculocutaneous_albinism|not_specified|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|TYR-related_disorder|Oculocutaneous_albinism|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism|TYR-related_disorder|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A": 3,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|TYR-related_disorder|not_provided": 1,
    "TYR-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided": 1,
    "not_provided|Oculocutaneous_albinism|Oculocutaneous_albinism_type_1A": 1,
    "Albinism_or_congenital_nystagmus|Oculocutaneous_albinism|not_specified|not_provided|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_specified|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|TYR-related_disorder|Oculocutaneous_albinism_type_1B|Albinism_or_congenital_nystagmus|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_1|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism": 1,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided": 1,
    "not_specified|not_provided|Oculocutaneous_albinism_type_1A": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_provided|Oculocutaneous_albinism_type_1": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|not_provided": 2,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism|not_specified|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism|not_provided": 1,
    "not_provided|TYR-related_disorder|Oculocutaneous_albinism_type_1|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|not_provided": 1,
    "Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism": 1,
    "TYR-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Albinism_or_congenital_nystagmus|Oculocutaneous_albinism|Inborn_genetic_diseases|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|TYR-related_disorder|Nonsyndromic_Oculocutaneous_Albinism|Ocular_albinism_with_congenital_sensorineural_hearing_loss|Oculocutaneous_albinism|not_provided|Oculocutaneous_albinism_type_1": 1,
    "Oculocutaneous_albinism|TYR-related_disorder|not_specified|not_provided": 1,
    "Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|not_provided": 2,
    "not_specified|not_provided|TYR-related_disorder": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|TYR-related_disorder": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism|not_provided|Oculocutaneous_albinism_type_1|See_cases": 1,
    "Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|not_specified": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided|Oculocutaneous_albinism_type_1": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_specified|not_provided": 1,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|Inborn_genetic_diseases|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|not_specified": 2,
    "Oculocutaneous_albinism|Oculocutaneous_albinism_type_1|Oculocutaneous_albinism_type_1A|TYR-related_disorder|not_provided": 1,
    "not_provided|Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "Albinism_or_congenital_nystagmus|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|TYR-related_disorder|Inborn_genetic_diseases|Nonsyndromic_Oculocutaneous_Albinism|Myopia|Albinism|Nystagmus|Oculocutaneous_albinism|not_provided|Abnormality_of_the_skin|See_cases": 1,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided|Oculocutaneous_albinism_type_1": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|not_provided|Oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|TYR-related_disorder|not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|Oculocutaneous_albinism|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism_type_1|not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Abnormality_of_the_skin": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Abnormality_of_the_eye": 1,
    "Oculocutaneous_albinism_type_1|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "not_provided|TYR-related_disorder|Inborn_genetic_diseases": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|TYR-related_disorder|Congenital_nystagmus|Albinism|Albinism_or_congenital_nystagmus|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_1|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B": 1,
    "Oculocutaneous_albinism_type_1A|not_provided|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|TYR-related_disorder|Oculocutaneous_albinism|not_provided": 2,
    "Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|TYR-related_disorder|Oculocutaneous_albinism|not_provided": 1,
    "Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism_type_1A": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|TYR-related_disorder|Nonsyndromic_Oculocutaneous_Albinism|Inborn_genetic_diseases|Oculocutaneous_albinism|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism|not_provided": 1,
    "Oculocutaneous_albinism|not_provided|Oculocutaneous_albinism_type_1": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|TYR-related_disorder": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|TYR-related_disorder|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_provided|Oculocutaneous_albinism": 1,
    "Albinism_or_congenital_nystagmus|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|TYR-related_disorder|Nonsyndromic_Oculocutaneous_Albinism|not_provided|Abnormality_of_the_skin": 1,
    "Foveal_hypoplasia|Elevated_circulating_hepatic_transaminase_concentration|Slow_decrease_in_visual_acuity|Albinism|Choroidal_neovascularization|Abnormality_of_metabolism/homeostasis|Autosomal_recessive_ocular_albinism|Pigmentary_skin_disorders|Albinism_or_congenital_nystagmus|Temperature-sensitive_oculocutaneous_albinism_type_1|not_specified|not_provided|Oculocutaneous_albinism_type_1|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Melanoma|_cutaneous_malignant|_susceptibility_to|_8|Skin/hair/eye_pigmentation_3|_blue/green_eyes|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Malignant_tumor_of_breast": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism|not_provided|Oculocutaneous_albinism_type_1": 1,
    "Inborn_genetic_diseases|not_provided|Oculocutaneous_albinism_type_1A": 1,
    "Inborn_genetic_diseases|Oculocutaneous_albinism|not_provided": 1,
    "Albinism_or_congenital_nystagmus|TYR-related_disorder|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|Ocular_albinism_with_congenital_sensorineural_hearing_loss|Oculocutaneous_albinism|Inborn_genetic_diseases|not_provided|Hearing_impairment|Abnormality_of_the_skin": 1,
    "Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism_type_1|not_provided": 1,
    "Albinism_or_congenital_nystagmus|Nonsyndromic_Oculocutaneous_Albinism|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|not_provided|Oculocutaneous_albinism_type_1": 1,
    "not_provided|Albinism|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "TYR-related_disorder|not_provided|Temperature-sensitive_oculocutaneous_albinism_type_1|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN": 1,
    "TYR-related_disorder|Oculocutaneous_albinism_type_1A|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_1B": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Albinism|Abnormal_retinal_morphology|Strabismus|Abnormal_optic_nerve_morphology|Horizontal_nystagmus|Hypopigmentation_of_the_skin|Ocular_albinism|Fair_hair|not_provided": 1,
    "Oculocutaneous_albinism_type_1|not_provided": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1B|Ocular_albinism_with_congenital_sensorineural_hearing_loss|not_specified|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|Oculocutaneous_albinism_type_1|not_provided": 1,
    "not_provided|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism": 1,
    "Oculocutaneous_albinism|Oculocutaneous_albinism_type_1": 1,
    "Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|not_specified": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_3|_LIGHT/DARK_SKIN|Oculocutaneous_albinism_type_1A|Oculocutaneous_albinism_type_1B|not_specified": 1,
    "FAT3-related_disorder": 60,
    "not_provided|FAT3-related_disorder": 14,
    "FAT3-related_disorder|not_specified": 2,
    "FAT3-related_disorder|not_provided": 15,
    "Familial_meningioma|FAT3-related_disorder": 1,
    "Familial_meningioma|not_provided": 8,
    "MTNR1B-related_disorder": 6,
    "MTNR1B-related_disorder|not_provided": 1,
    "Seckel_syndrome_11": 4,
    "CEP295-related_condition": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|MED17-related_disorder": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 76,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 9,
    "not_provided|MED17-related_disorder|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 2,
    "not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 19,
    "Inborn_genetic_diseases|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|not_provided|MED17-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 2,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|not_provided": 10,
    "not_specified|MED17-related_disorder|not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "not_specified|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|not_specified|not_provided|MED17-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "not_provided|not_specified|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|not_provided|MED17-related_disorder": 1,
    "not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|MED17-related_disorder": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|Inborn_genetic_diseases|not_provided": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|not_specified|not_provided": 1,
    "not_provided|MED17-related_disorder": 1,
    "MED17-related_disorder|not_specified|Microcephaly|not_provided": 1,
    "Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly|MED17-related_disorder|not_provided": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|Infantile_cerebral_and_cerebellar_atrophy_with_postnatal_progressive_microcephaly": 1,
    "HEPHL1-related_disorder": 10,
    "Pili_torti-developmental_delay-neurological_abnormalities_syndrome": 6,
    "HEPHL1-related_disorder|Pili_torti-developmental_delay-neurological_abnormalities_syndrome|not_provided": 2,
    "HEPHL1-related_disorder|not_provided": 2,
    "not_provided|HEPHL1-related_disorder": 1,
    "Pili_torti-developmental_delay-neurological_abnormalities_syndrome|not_provided": 1,
    "Lichen_planopilaris": 1,
    "Oocyte_maturation_defect_7|not_provided": 1,
    "Oocyte_maturation_defect_7": 8,
    "PANX1-related_disorder": 4,
    "not_specified|Oocyte_maturation_defect_7": 1,
    "PANX1-related_disorder|not_provided": 2,
    "not_provided|PANX1-related_disorder": 2,
    "not_provided|PANX1-related_disorder|Oocyte_maturation_defect_7": 1,
    "Ataxia-telangiectasia-like_disorder_1": 103,
    "not_provided|Ataxia-telangiectasia-like_disorder_1": 7,
    "Ataxia-telangiectasia-like_disorder_1|not_provided": 3,
    "Malignant_tumor_of_urinary_bladder|Ataxia-telangiectasia-like_disorder_1": 1,
    "Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 11,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 192,
    "Ataxia-telangiectasia-like_disorder": 348,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 192,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 20,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Ataxia-telangiectasia-like_disorder_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|not_provided|Ataxia-telangiectasia-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1": 20,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder": 9,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder_1": 15,
    "Ataxia-telangiectasia-like_disorder_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder|MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 3,
    "Ataxia-telangiectasia-like_disorder|MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 10,
    "Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome": 21,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1": 6,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1|not_provided|Ataxia-telangiectasia-like_disorder|not_specified": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_provided": 8,
    "Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder": 22,
    "Ataxia-telangiectasia-like_disorder|MRE11-related_disorder": 1,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1": 9,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia-like_disorder_1": 9,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome": 12,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|MRE11-related_disorder": 1,
    "not_specified|Ataxia-telangiectasia-like_disorder|not_provided|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|MRE11-related_disorder|not_specified|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1": 11,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1": 1,
    "not_provided|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 2,
    "Ataxia-telangiectasia-like_disorder|not_provided|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Ataxia-telangiectasia-like_disorder_1|Parkinsonian_disorder|Dystonic_disorder|Dementia|Depression": 1,
    "Colonic_neoplasm|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder_1": 1,
    "MRE11-related_disorder|See_cases|not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|MRE11-related_disorder": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder": 9,
    "not_specified|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_provided|Ataxia-telangiectasia-like_disorder_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 4,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Breast_carcinoma|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "not_provided|Ataxia-telangiectasia-like_disorder": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|MRE11-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia-like_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MRE11-related_disorder|Ataxia-telangiectasia-like_disorder": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia-like_disorder_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_provided": 4,
    "Malignant_tumor_of_urinary_bladder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "Ataxia-telangiectasia-like_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|not_specified|Ataxia-telangiectasia-like_disorder|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|Breast_carcinoma": 1,
    "not_specified|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_specified|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder|MRE11-related_disorder|Ataxia-telangiectasia-like_disorder_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia-like_disorder_1|not_provided|Ovarian_cancer": 1,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "MRE11-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia-like_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|not_specified|not_provided": 2,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder_1|not_provided|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_specified": 1,
    "Ataxia-telangiectasia-like_disorder|MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder_1": 1,
    "See_cases|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "Triple-negative_breast_cancer": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|not_provided": 3,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder|not_specified|Ataxia-telangiectasia-like_disorder_1": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|not_specified|Ovarian_neoplasm|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia-like_disorder": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Ataxia-telangiectasia-like_disorder": 1,
    "Eccrine_porocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Ataxia-telangiectasia-like_disorder": 1,
    "MRE11-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 3,
    "Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Renal_transitional_cell_carcinoma|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "not_provided|Ataxia-telangiectasia-like_disorder|not_specified|Ataxia-telangiectasia-like_disorder_1|Hereditary_breast_ovarian_cancer_syndrome|MRE11-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder_1|not_provided|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "MRE11-related_disorder|Ataxia-telangiectasia-like_disorder": 1,
    "not_provided|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|Ataxia-telangiectasia-like_disorder_1": 1,
    "MRE11-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder|not_provided|Ataxia-telangiectasia-like_disorder_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|Premature_ovarian_insufficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MRE11-related_disorder": 1,
    "not_specified|Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder_1|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1": 1,
    "Ataxia-telangiectasia-like_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia-like_disorder_1|Dementia|Depression|Dystonic_disorder|Parkinsonian_disorder": 1,
    "not_provided|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia-like_disorder": 1,
    "Ataxia-telangiectasia-like_disorder_1|not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|not_specified": 1,
    "not_provided|MRE11-related_disorder|Ataxia-telangiectasia-like_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia-like_disorder_1|Ataxia-telangiectasia-like_disorder|not_specified": 1,
    "not_provided|Ataxia-telangiectasia-like_disorder_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia-like_disorder_1|not_specified": 1,
    "CRANIOFACIOCARDIOHEPATIC_SYNDROME": 2,
    "CRANIOFACIOCARDIOHEPATIC_SYNDROME|not_provided": 1,
    "CRANIOFACIOCARDIOHEPATIC_SYNDROME|AMOTL1-associated_disorder": 1,
    "AMOTL1-associated_disorder": 1,
    "not_specified|CRANIOFACIOCARDIOHEPATIC_SYNDROME|not_provided|Tethered_cord|Cleft_lip/palate|Hypertelorism|imperforate_anus_with_fistula|Long_fingers|Abnormal_pinna_morphology": 1,
    "Mosaic_variegated_aneuploidy_syndrome_2": 230,
    "Mosaic_variegated_aneuploidy_syndrome_2|Inborn_genetic_diseases": 117,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_2": 110,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_2": 4,
    "Mosaic_variegated_aneuploidy_syndrome_2|not_provided": 4,
    "not_specified|Mosaic_variegated_aneuploidy_syndrome_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_2": 1,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_2|not_provided": 1,
    "Mosaic_variegated_aneuploidy_syndrome_2|Inborn_genetic_diseases|not_provided": 3,
    "Mosaic_variegated_aneuploidy_syndrome_2|CEP57-related_disorder|Inborn_genetic_diseases": 1,
    "Mosaic_variegated_aneuploidy_syndrome": 2,
    "Inborn_genetic_diseases|CEP57-related_disorder|Mosaic_variegated_aneuploidy_syndrome_2": 1,
    "Mosaic_variegated_aneuploidy_syndrome_2|CEP57-related_disorder|not_provided": 1,
    "not_provided|CEP57-related_disorder|Mosaic_variegated_aneuploidy_syndrome_2": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Mosaic_variegated_aneuploidy_syndrome_2|not_provided": 1,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_2|Inborn_genetic_diseases": 1,
    "CEP57-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|not_provided": 11,
    "Charcot-Marie-Tooth_disease_type_4B1": 65,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B1": 7,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B1|not_provided": 1,
    "MTMR2-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 2,
    "MTMR2-related_disorder|Charcot-Marie-Tooth_disease_type_4": 2,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B1|not_provided|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|MTMR2-related_disorder|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|MTMR2-related_disorder|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B1|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease_type_4": 4,
    "Charcot-Marie-Tooth_disease_type_4B1|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B1|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|MTMR2-related_disorder|Charcot-Marie-Tooth_disease|not_specified": 1,
    "MTMR2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B1|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "MTMR2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B1|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B1|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4B1|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B1": 1,
    "CCDC82-related_disorder": 1,
    "CNTN5-related_disorder": 20,
    "not_provided|CNTN5-related_disorder": 2,
    "CNTN5-related_Neurodevelopmental_disorder": 1,
    "CNTN5-related_disorder|not_specified": 2,
    "CNTN5-related_disorder|not_provided": 2,
    "Focal_segmental_glomerulosclerosis_2": 161,
    "not_provided|Focal_segmental_glomerulosclerosis_2": 22,
    "not_provided|Focal_segmental_glomerulosclerosis_2|TRPC6-related_disorder|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_2|not_provided": 18,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_2": 3,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_2": 2,
    "TRPC6-related_disorder|Focal_segmental_glomerulosclerosis_2|Nephrotic_syndrome": 1,
    "TRPC6-related_disorder|Nephrotic_syndrome|not_provided|Focal_segmental_glomerulosclerosis_2": 1,
    "Focal_segmental_glomerulosclerosis_2|not_provided|not_specified": 1,
    "TRPC6-related_disorder|not_provided": 3,
    "TRPC6-related_disorder": 9,
    "not_provided|Focal_segmental_glomerulosclerosis_2|not_specified": 3,
    "Kidney_disorder|Focal_segmental_glomerulosclerosis_2|not_provided": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_2|not_provided": 1,
    "TRPC6-related_disorder|Focal_segmental_glomerulosclerosis_2|Focal_segmental_glomerulosclerosis": 1,
    "Focal_segmental_glomerulosclerosis_2|Inborn_genetic_diseases": 8,
    "Focal_segmental_glomerulosclerosis_2|Inborn_genetic_diseases|not_provided": 2,
    "Focal_segmental_glomerulosclerosis_2|not_provided|Inborn_genetic_diseases": 3,
    "Prednisolone_response|not_specified|Focal_segmental_glomerulosclerosis_2|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "Focal_segmental_glomerulosclerosis_2|not_specified|TRPC6-related_disorder|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|not_provided|not_specified|Focal_segmental_glomerulosclerosis_2": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_2": 1,
    "not_provided|TRPC6-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_2|not_provided|TRPC6-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_2": 4,
    "Corticosteroids_response|Focal_segmental_glomerulosclerosis_2": 1,
    "not_specified|TRPC6-related_disorder|not_provided|Focal_segmental_glomerulosclerosis_2": 1,
    "not_specified|Focal_segmental_glomerulosclerosis|not_provided|Focal_segmental_glomerulosclerosis_2": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis": 3,
    "not_provided|Focal_segmental_glomerulosclerosis_2|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_2|Inborn_genetic_diseases": 1,
    "Nephrotic_syndrome|Focal_segmental_glomerulosclerosis_2": 1,
    "Focal_segmental_glomerulosclerosis_2|not_provided|TRPC6-related_disorder|Nephrotic_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_2": 2,
    "Focal_segmental_glomerulosclerosis_2|not_provided|TRPC6-related_disorder": 1,
    "not_provided|TRPC6-related_disorder|Focal_segmental_glomerulosclerosis_2": 1,
    "TRPC6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TRPC6-related_disorder": 1,
    "not_provided|not_specified|Kidney_disorder|Focal_segmental_glomerulosclerosis_2": 1,
    "Focal_segmental_glomerulosclerosis_2|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "CFAP300-related_disorder|not_provided": 4,
    "Ciliary_dyskinesia|_primary|_38": 5,
    "Ciliary_dyskinesia|_primary|_38|not_provided": 5,
    "not_provided|Ciliary_dyskinesia|_primary|_38": 1,
    "CFAP300-related_disorder": 2,
    "Ciliary_dyskinesia|_primary|_38|CFAP300-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|YAP1-related_disorder": 2,
    "Uveal_coloboma-cleft_lip_and_palate-intellectual_disability": 7,
    "not_provided|YAP1-related_disorder|not_specified": 1,
    "YAP1-related_disorder": 3,
    "not_provided|Uveal_coloboma-cleft_lip_and_palate-intellectual_disability|YAP1-related_disorder": 1,
    "YAP1-related_disorder|not_provided": 2,
    "Uveal_coloboma-cleft_lip_and_palate-intellectual_disability|not_provided": 1,
    "Thalidomide_response|not_provided": 1,
    "BIRC2-related_disorder": 1,
    "Amelogenesis_imperfecta_hypomaturation_type_2A2": 43,
    "Amelogenesis_Imperfecta|_Recessive": 39,
    "Amelogenesis_imperfecta_hypomaturation_type_2A2|not_provided": 6,
    "Amelogenesis_imperfecta_hypomaturation_type_2A2|Inborn_genetic_diseases": 3,
    "not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A2": 5,
    "MMP20-related_disorder": 4,
    "Amelogenesis_imperfecta_hypomaturation_type_2A2|Intellectual_disability|_autosomal_dominant_56": 1,
    "Inborn_genetic_diseases|Amelogenesis_imperfecta_hypomaturation_type_2A2": 2,
    "MMP20-related_disorder|Inborn_genetic_diseases|not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A2": 1,
    "Amelogenesis_Imperfecta|_Recessive|not_provided": 15,
    "Amelogenesis_imperfecta_hypomaturation_type_2A2|Inborn_genetic_diseases|not_provided": 1,
    "MMP20-related_disorder|Amelogenesis_imperfecta_hypomaturation_type_2A2": 1,
    "not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A2|not_specified": 1,
    "not_specified|not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A2": 1,
    "MMP20-related_disorder|not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A2": 1,
    "not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A2|MMP20-related_disorder": 1,
    "Amelogenesis_imperfecta_hypomaturation_type_2A2|not_specified|not_provided": 1,
    "not_provided|MMP1-related_disorder": 1,
    "MMP1-related_disorder": 5,
    "COPD|_severe_early_onset|Recessive_dystrophic_epidermolysis_bullosa|not_provided|MMP1-related_disorder": 1,
    "not_provided|Preterm_premature_rupture_of_membranes": 1,
    "PULMONARY_DISEASE|_CHRONIC_OBSTRUCTIVE|_RATE_OF_DECLINE_OF_LUNG_FUNCTION_IN": 1,
    "not_provided|MMP3-related_disorder": 2,
    "MMP3-related_disorder": 2,
    "Coronary_heart_disease|_susceptibility_to|_6": 1,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_anadysplasia": 15,
    "Metaphyseal_anadysplasia|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 10,
    "Spondyloepimetaphyseal_dysplasia|Metaphyseal_anadysplasia|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_anadysplasia|not_provided": 5,
    "Spondyloepimetaphyseal_dysplasia|Metaphyseal_anadysplasia": 2,
    "Metaphyseal_chondrodysplasia|_Spahr_type": 3,
    "Intellectual_disability|Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_chondrodysplasia|_Spahr_type|not_provided": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_anadysplasia|Metaphyseal_chondrodysplasia|_Spahr_type": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_anadysplasia": 8,
    "MMP13-related_disorder|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_anadysplasia|Metaphyseal_chondrodysplasia|_Spahr_type|not_provided": 1,
    "not_provided|MMP13-related_disorder": 2,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_anadysplasia|not_provided|not_specified": 2,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_chondrodysplasia|_Spahr_type": 1,
    "Metaphyseal_chondrodysplasia|_Spahr_type|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 1,
    "not_provided|Metaphyseal_anadysplasia|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 3,
    "Metaphyseal_anadysplasia|not_provided|Spondyloepimetaphyseal_dysplasia|_Missouri_type|Metaphyseal_chondrodysplasia|_Spahr_type": 1,
    "Metaphyseal_anadysplasia|not_provided|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 2,
    "not_specified|Metaphyseal_anadysplasia|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 1,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type": 5,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 3,
    "Metaphyseal_chondrodysplasia|_Spahr_type|not_provided|Metaphyseal_anadysplasia_1|_autosomal_dominant": 1,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|not_provided|Metaphyseal_anadysplasia": 1,
    "not_provided|Metaphyseal_chondrodysplasia|_Spahr_type|Spondyloepimetaphyseal_dysplasia|_Missouri_type": 1,
    "Metaphyseal_chondrodysplasia|_Spahr_type|Spondyloepimetaphyseal_dysplasia|_Missouri_type|not_provided|Metaphyseal_anadysplasia_1|_autosomal_dominant": 1,
    "Metaphyseal_anadysplasia_1|_autosomal_dominant": 2,
    "Spondyloepimetaphyseal_dysplasia|_Missouri_type|not_provided": 1,
    "Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 18,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 58,
    "Jeune_thoracic_dystrophy|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3": 8,
    "not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 10,
    "Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy|not_provided|not_specified|Asphyxiating_thoracic_dystrophy_3": 1,
    "Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases": 6,
    "Asphyxiating_thoracic_dystrophy_2|Short_rib-polydactyly_syndrome|not_specified|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_3": 10,
    "Retinal_dystrophy|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_provided": 6,
    "Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 1,
    "Asphyxiating_thoracic_dystrophy_1|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 66,
    "Jeune_thoracic_dystrophy|not_specified": 19,
    "DYNC2H1-related_disorder": 17,
    "Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases|Short_rib-polydactyly_syndrome": 3,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases|not_provided": 1,
    "Jeune_thoracic_dystrophy|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 3,
    "Asphyxiating_thoracic_dystrophy_3|not_provided|Jeune_thoracic_dystrophy|DYNC2H1-related_disorder": 1,
    "not_specified|Asphyxiating_thoracic_dystrophy_3": 6,
    "Asphyxiating_thoracic_dystrophy_3|not_provided|Jeune_thoracic_dystrophy": 6,
    "DYNC2H1-related_disorder|not_specified": 1,
    "Jeune_thoracic_dystrophy|not_provided|not_specified|Asphyxiating_thoracic_dystrophy_3": 5,
    "Jeune_thoracic_dystrophy|Retinal_dystrophy": 4,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_specified": 2,
    "Intellectual_disability|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|Inborn_genetic_diseases|Short_rib-polydactyly_syndrome": 1,
    "not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 2,
    "not_provided|Jeune_thoracic_dystrophy|Inborn_genetic_diseases": 6,
    "not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 2,
    "not_specified|not_provided|Short_rib-polydactyly_syndrome|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|Retinal_dystrophy|not_provided|not_specified|Asphyxiating_thoracic_dystrophy_3|Intellectual_disability": 1,
    "Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 13,
    "Jeune_thoracic_dystrophy|not_provided|DYNC2H1-related_disorder|Asphyxiating_thoracic_dystrophy_3": 1,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 16,
    "not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 3,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_3|not_specified": 4,
    "not_specified|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 3,
    "Asphyxiating_thoracic_dystrophy_3|not_specified|not_provided|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 9,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_provided": 5,
    "DYNC2H1-related_disorder|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 4,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_specified|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3": 2,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3|Intellectual_disability": 1,
    "DYNC2H1-related_disorder|Asphyxiating_thoracic_dystrophy_3": 1,
    "Retinal_dystrophy|Jeune_thoracic_dystrophy": 2,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided": 6,
    "Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder": 2,
    "Jeune_thoracic_dystrophy|DYNC2H1-related_disorder|not_specified|not_provided": 2,
    "not_provided|Jeune_thoracic_dystrophy|Short_rib-polydactyly_syndrome": 1,
    "Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3": 4,
    "not_provided|not_specified|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 6,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 2,
    "DYNC2H1-related_disorder|not_specified|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|DYNC2H1-related_disorder": 1,
    "Jeune_thoracic_dystrophy|DYNC2H1-related_disorder": 9,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided|not_specified": 2,
    "DYNC2H1-related_disorder|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Retinal_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_specified|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|not_provided|not_specified": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3": 2,
    "not_provided|Asphyxiating_thoracic_dystrophy_3|not_specified|Jeune_thoracic_dystrophy|Intellectual_disability|DYNC2H1-related_disorder": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided|Short_rib-polydactyly_syndrome": 2,
    "not_provided|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 1,
    "not_provided|Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3": 2,
    "Asphyxiating_thoracic_dystrophy_3|not_provided|not_specified|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 2,
    "Inborn_genetic_diseases|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Retinal_dystrophy": 1,
    "Optic_atrophy|not_specified|Jeune_thoracic_dystrophy|Retinal_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|Short_rib-polydactyly_syndrome": 2,
    "Jeune_thoracic_dystrophy|DYNC2H1-related_disorder|not_specified": 1,
    "Intellectual_disability|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Intellectual_disability|Jeune_thoracic_dystrophy": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 3,
    "Jeune_thoracic_dystrophy|DYNC2H1-related_disorder|not_provided": 2,
    "Asphyxiating_thoracic_dystrophy_3|not_specified|Jeune_thoracic_dystrophy": 3,
    "Short_rib-polydactyly_syndrome|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_specified": 1,
    "not_specified|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 1,
    "Short_rib-polydactyly_syndrome|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|not_provided": 3,
    "Asphyxiating_thoracic_dystrophy_3|not_specified|Jeune_thoracic_dystrophy|not_provided": 2,
    "DYNC2H1-related_disorder|Asphyxiating_thoracic_dystrophy_3|not_provided|Jeune_thoracic_dystrophy": 2,
    "not_provided|not_specified|Jeune_thoracic_dystrophy": 1,
    "not_specified|not_provided|Jeune_thoracic_dystrophy": 2,
    "not_specified|Asphyxiating_thoracic_dystrophy_3|not_provided|Inborn_genetic_diseases|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_3|not_provided": 5,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|Short_rib-polydactyly_syndrome": 2,
    "Jeune_thoracic_dystrophy|Short_rib-polydactyly_syndrome": 7,
    "Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 5,
    "not_provided|not_specified|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_specified": 2,
    "Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases|not_provided|Jeune_thoracic_dystrophy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10": 580,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|not_provided": 2,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_specified": 3,
    "DYNC2H1-related_disorder|not_specified|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Optic_atrophy|Neonatal_respiratory_distress": 1,
    "Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases|not_provided|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_specified|not_provided": 1,
    "not_specified|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Heart|_malformation_of|Deformed_rib_cage|Short_ribs|Short_long_bone|Abnormality_of_the_lung": 2,
    "not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_specified": 1,
    "Autosomal_dominant_Robinow_syndrome_2|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|DYNC2H1-related_disorder": 1,
    "Type_IV_short_rib_polydactyly_syndrome|Jeune_thoracic_dystrophy|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_specified|not_provided|Jeune_thoracic_dystrophy|Inborn_genetic_diseases": 2,
    "not_specified|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 2,
    "Intellectual_disability|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Asphyxiating_thoracic_dystrophy_3|not_specified|not_provided|Jeune_thoracic_dystrophy": 2,
    "not_specified|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 2,
    "not_specified|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3": 1,
    "Retinal_dystrophy|Short_rib-polydactyly_syndrome|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 7,
    "Inborn_genetic_diseases|not_provided|Jeune_thoracic_dystrophy": 2,
    "Jeune_thoracic_dystrophy|not_provided|Inborn_genetic_diseases": 3,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|not_specified|not_provided": 3,
    "Jeune_thoracic_dystrophy|DYNC2H1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Short_rib-polydactyly_syndrome|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 2,
    "Asphyxiating_thoracic_dystrophy_3|not_provided|not_specified": 1,
    "Jeune_thoracic_dystrophy|DYNC2H1-related_disorder|Inborn_genetic_diseases": 1,
    "Asphyxiating_thoracic_dystrophy_3|not_provided|not_specified|Jeune_thoracic_dystrophy": 1,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_provided": 1,
    "Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|not_provided|DYNC2H1-related_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_specified": 3,
    "DYNC2H1-related_disorder|not_provided|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder": 2,
    "Retinal_dystrophy|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_specified|Short_rib-polydactyly_syndrome": 1,
    "Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 1,
    "Jeune_thoracic_dystrophy|not_provided|not_specified|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 1,
    "not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|Retinal_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|DYNC2H1-related_disorder": 1,
    "Jeune_thoracic_dystrophy|not_specified|not_provided|DYNC2H1-related_disorder": 1,
    "DYNC2H1-related_disorder|not_specified|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3|Renal_cyst": 1,
    "DYNC2H1-related_disorder|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy": 1,
    "not_specified|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "not_provided|DYNC2H1-related_disorder": 1,
    "Short_rib-polydactyly_syndrome|Bowing_of_the_long_bones|Narrow_chest|Fetal_growth_restriction|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "Neonatal_respiratory_distress|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder": 1,
    "Jeune_thoracic_dystrophy|not_provided|DYNC2H1-related_disorder": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_provided|not_specified|Short_rib-polydactyly_syndrome": 1,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 2,
    "not_provided|Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 2,
    "Jeune_thoracic_dystrophy|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Micrognathia|Clinodactyly|Short_long_bone|Short_ribs|Narrow_chest": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Optic_atrophy|not_provided": 1,
    "Inborn_genetic_diseases|DYNC2H1-related_disorder|not_provided": 1,
    "Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy|not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "DYNC2H1-related_disorder|not_provided|Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3": 1,
    "Retinal_dystrophy|Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Jeune_thoracic_dystrophy": 1,
    "Autosomal_recessive_polycystic_kidney_disease|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 1,
    "not_specified|not_provided|DYNC2H1-related_disorder|Intellectual_disability|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|Intellectual_disability": 1,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|Jeune_thoracic_dystrophy|not_specified": 2,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_provided": 1,
    "not_provided|not_specified|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 1,
    "Fetal_growth_restriction|Narrow_chest|Bowing_of_the_long_bones": 1,
    "Short_rib-polydactyly_syndrome|Inborn_genetic_diseases|Asphyxiating_thoracic_dystrophy_3": 1,
    "DYNC2H1-related_disorder|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_provided|Retinitis_pigmentosa|Asphyxiating_thoracic_dystrophy_4|Retinal_dystrophy|Asphyxiating_thoracic_dystrophy_3": 1,
    "Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_specified|not_provided": 2,
    "not_specified|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_provided|Short_rib-polydactyly_syndrome": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|not_specified": 1,
    "not_specified|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|DYNC2H1-related_disorder|Short_rib-polydactyly_syndrome|Inborn_genetic_diseases": 1,
    "DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_specified|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Jeune_thoracic_dystrophy|Inborn_genetic_diseases|Retinal_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Retinal_dystrophy|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 1,
    "DYNC2H1-related_disorder|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|Short_rib-polydactyly_syndrome|Jeune_thoracic_dystrophy": 1,
    "not_specified|Short_rib-polydactyly_syndrome|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 1,
    "not_specified|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "Jeune_thoracic_dystrophy|Retinal_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided|not_specified": 1,
    "Intellectual_disability|DYNC2H1-related_disorder|not_provided|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Inborn_genetic_diseases": 1,
    "DYNC2H1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|Short_rib-polydactyly_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 2,
    "Short_rib-polydactyly_syndrome|Retinal_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Asphyxiating_thoracic_dystrophy_3": 1,
    "Short_rib-polydactyly_syndrome|Hirschsprung_disease|_susceptibility_to|_1|DYNC2H1-related_disorder|Jeune_thoracic_dystrophy|not_specified": 1,
    "Jeune_thoracic_dystrophy|not_provided|Asphyxiating_thoracic_dystrophy_3|not_specified": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|not_provided|not_specified": 1,
    "DYNC2H1-related_disorder|not_provided|Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy": 1,
    "Asphyxiating_thoracic_dystrophy_3|Jeune_thoracic_dystrophy|Short_rib-polydactyly_syndrome": 1,
    "Retinal_dystrophy|not_provided|Inborn_genetic_diseases|Jeune_thoracic_dystrophy": 1,
    "Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|DYNC2H1-related_disorder|not_provided": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Jeune_thoracic_dystrophy": 1,
    "Short-rib_thoracic_dysplasia_6_with_or_without_polydactyly|not_specified|Jeune_thoracic_dystrophy": 1,
    "Short_rib-polydactyly_syndrome|Inborn_genetic_diseases|Jeune_thoracic_dystrophy|Asphyxiating_thoracic_dystrophy_3|not_provided": 1,
    "CASP12-related_disorder": 8,
    "not_provided|CASP12-related_disorder|not_specified": 1,
    "Sepsis|_susceptibility_to": 1,
    "CASP1-related_disorder": 2,
    "GRIA4-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities": 34,
    "GRIA4-related_disorder": 12,
    "See_cases|Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities": 1,
    "GRIA4-related_neurodevelopmental_disorder": 2,
    "Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities|Inborn_genetic_diseases": 3,
    "not_provided|GRIA4-related_disorder": 3,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities": 1,
    "not_provided|GRIA4-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities": 1,
    "Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities|Intellectual_disability": 4,
    "Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities|Inborn_genetic_diseases|Intellectual_disability": 1,
    "GRIA4-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_seizures_and_gait_abnormalities|GRIA4-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_71": 17,
    "ALKBH8-related_disorder": 9,
    "Intellectual_developmental_disorder|_autosomal_recessive_71|ALKBH8-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_71|not_provided": 2,
    "ALKBH8-related_disorder|not_provided": 3,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_71": 1,
    "ALKBH8-related_disorder|not_specified": 1,
    "not_provided|not_specified|Intellectual_developmental_disorder|_autosomal_recessive_71": 1,
    "not_provided|ALKBH8-related_disorder": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_71|ALKBH8-related_disorder|not_provided": 2,
    "Intellectual_developmental_disorder|_autosomal_recessive_71|not_specified": 1,
    "not_specified|not_provided|ALKBH8-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_71|not_provided|ALKBH8-related_disorder": 1,
    "ALKBH8-related_disorder|not_specified|not_provided": 1,
    "Deficiency_of_acetyl-CoA_acetyltransferase": 616,
    "Deficiency_of_acetyl-CoA_acetyltransferase|not_provided": 16,
    "not_provided|Deficiency_of_acetyl-CoA_acetyltransferase": 25,
    "Deficiency_of_acetyl-CoA_acetyltransferase|not_specified": 6,
    "not_provided|not_specified|Deficiency_of_acetyl-CoA_acetyltransferase": 2,
    "not_specified|not_provided|Deficiency_of_acetyl-CoA_acetyltransferase": 1,
    "Deficiency_of_acetyl-CoA_acetyltransferase|ACAT1-related_disorder": 3,
    "Deficiency_of_acetyl-CoA_acetyltransferase|Inborn_genetic_diseases": 6,
    "ACAT1-related_disorder|Deficiency_of_acetyl-CoA_acetyltransferase|not_provided": 1,
    "ACAT1-related_disorder": 3,
    "Deficiency_of_acetyl-CoA_acetyltransferase|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Deficiency_of_acetyl-CoA_acetyltransferase": 3,
    "Inborn_genetic_diseases|Deficiency_of_acetyl-CoA_acetyltransferase": 7,
    "not_provided|Deficiency_of_acetyl-CoA_acetyltransferase|Inborn_genetic_diseases": 2,
    "ACAT1-related_disorder|not_provided|Deficiency_of_acetyl-CoA_acetyltransferase": 2,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_acetyl-CoA_acetyltransferase": 1,
    "not_provided|ACAT1-related_disorder|Deficiency_of_acetyl-CoA_acetyltransferase": 1,
    "Deficiency_of_acetyl-CoA_acetyltransferase|not_provided|not_specified": 3,
    "Deficiency_of_acetyl-CoA_acetyltransferase|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deficiency_of_acetyl-CoA_acetyltransferase|not_provided": 1,
    "NPAT-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|NPAT-related_disorder": 1,
    "Ataxia-telangiectasia_syndrome": 4627,
    "not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 7,
    "not_provided|Ataxia-telangiectasia_syndrome": 77,
    "not_specified|Ataxia-telangiectasia_syndrome": 46,
    "ATM-related_cancer_predisposition": 14,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided": 66,
    "Ataxia-telangiectasia_syndrome|not_specified": 36,
    "Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition": 7,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Familial_cancer_of_breast|ATM-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder": 21,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 26,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 639,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|See_cases|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 131,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast": 6,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1803,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 37,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1121,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 65,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 327,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 176,
    "Ataxia_telangiectasi": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 387,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 33,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 93,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 93,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 280,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 34,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 125,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 225,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 205,
    "Familial_cancer_of_breast|not_provided|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 46,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 202,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 15,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 3,
    "Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 309,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 16,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome": 2,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 8,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 9,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|See_cases": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 17,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 61,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 64,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 4,
    "Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 5,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Tip-toe_gait|Breast_cancer|_susceptibility_to": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_disorder|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 27,
    "Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 8,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 5,
    "not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 24,
    "Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_colorectal_cancer_type_X|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_colon|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 38,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_carcinoma": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 3,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Gastric_cancer": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 27,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 37,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast": 20,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 15,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 12,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified": 2,
    "not_specified|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 14,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 5,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 2,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 12,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 4,
    "Ataxia-telangiectasia_syndrome|not_provided|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 5,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 21,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 7,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 2,
    "Breast_cancer|_susceptibility_to|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 6,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified": 11,
    "Carcinoma_of_colon|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 27,
    "Ataxia-telangiectasia_syndrome|not_provided": 57,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 4,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 11,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 5,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Gastric_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 12,
    "Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome": 8,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 22,
    "Hereditary_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia_-_telangiectasia_variant|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 24,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 13,
    "Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 33,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 6,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Ataxia-telangiectasia_syndrome|ATM-related_disorder|Familial_colorectal_cancer_type_X": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 4,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 8,
    "Ataxia-telangiectasia_syndrome|Gastric_cancer": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Familial_cancer_of_breast|ATM-related_cancer_predisposition": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 7,
    "ATM-related_disorder|Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Malignant_neoplasm_of_brain": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|See_cases": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 15,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 11,
    "Familial_colorectal_cancer_type_X|not_specified|Ataxia-telangiectasia_syndrome": 2,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 266,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Conjunctival_telangiectasia|Oculomotor_apraxia|Cerebellar_ataxia|Immunodeficiency": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 3,
    "Ataxia-telangiectasia_syndrome|ATM-related_disorder": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 14,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 3,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|ATM-related_cancer_predisposition|ATM-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 3,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Incidental_Discovery": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified": 11,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 9,
    "Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Abnormal_central_motor_function|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "Breast_carcinoma|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Gastric_cancer|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified": 4,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 8,
    "Familial_cancer_of_breast|PANCREATIC_CANCER|_SUSCEPTIBILITY_TO|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 13,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 17,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Ataxia-telangiectasia_syndrome": 11,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 9,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified": 27,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Malignant_tumor_of_breast|Intellectual_disability": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 3,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome": 3,
    "ATM-related_cancer_predisposition|Bile_duct_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Intellectual_disability": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 1,
    "ATM-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 2,
    "not_specified|Breast_and/or_ovarian_cancer|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|Familial_cancer_of_breast": 5,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_disorder": 2,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Ataxia-telangiectasia_syndrome": 2,
    "Familial_colorectal_cancer_type_X|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|not_provided": 3,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Gastric_cancer|Breast_cancer|_susceptibility_to|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 1,
    "Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast": 6,
    "Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Abnormal_central_motor_function|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ATM-related_cancer_predisposition|Familial_colorectal_cancer_type_X|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 1,
    "ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 6,
    "Breast_cancer|_susceptibility_to|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Abnormal_central_motor_function|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 13,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 4,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition": 6,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|ATM-related_cancer_predisposition|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Tip-toe_gait|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Hepatoblastoma|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 2,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "Familial_colorectal_cancer_type_X|ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified": 5,
    "Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 6,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome": 9,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 5,
    "not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 6,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome": 17,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 7,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Gastric_cancer|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Familial_colorectal_cancer_type_X": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 23,
    "Gastric_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 6,
    "Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "ATM-related_disorder|Bilateral_breast_carcinoma|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "not_provided|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome": 3,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "Ataxia-telangiectasia_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 6,
    "Gastric_cancer|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 8,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_disorder|not_specified|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 15,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Endometrial_carcinoma|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Ataxia-telangiectasia_syndrome": 3,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 2,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|ATM-related_disorder": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified": 5,
    "not_specified|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 3,
    "Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|ATM-related_cancer_predisposition|not_provided|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Ovarian_cancer|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Neoplasm": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer": 2,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|See_cases": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 3,
    "Gastric_cancer|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_colon|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Tip-toe_gait": 1,
    "Colorectal_cancer|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 9,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 2,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Familial_colorectal_cancer_type_X|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X": 3,
    "ATM-related_disorder|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Familial_colorectal_cancer_type_X|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Microcephaly": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Cancer_or_benign_tumor|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome": 9,
    "Familial_cancer_of_breast|Familial_colorectal_cancer_type_X": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 2,
    "not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer_type_X|not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 3,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|ATM-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_cancer_predisposition": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Hereditary_cancer|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|ATM-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 4,
    "not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|ATM-related_disorder|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 14,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified": 2,
    "Ataxia-telangiectasia_syndrome|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 9,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder": 2,
    "Gastric_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|B-cell_non-Hodgkin_lymphoma|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Carcinoma_of_colon|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Diffuse_hemispheric_glioma|_H3_G34-mutant": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome|Breast_cancer|_susceptibility_to|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified": 6,
    "not_specified|Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Cerebellar_ataxia|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|ATM-related_cancer_predisposition|Breast_cancer|_susceptibility_to|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Endometrial_carcinoma|Ataxia-telangiectasia_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 2,
    "Familial_colorectal_cancer_type_X|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Microcephaly": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 3,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "ATM-related_disorder|not_specified|not_provided|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|ATM-related_disorder|Familial_ovarian_cancer": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 3,
    "ATM-related_cancer_predisposition|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|not_provided": 1,
    "Malignant_tumor_of_pancreas|ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified": 3,
    "Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Ovarian_carcinoma": 1,
    "ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 2,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tip-toe_gait|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Gastric_cancer|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|ATM-related_cancer_predisposition_syndrome|ATM-related_disorder|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 2,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|ATM-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiac_valvular_dysplasia|_X-linked|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 4,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 2,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ataxia-telangiectasia_syndrome": 2,
    "Familial_cancer_of_breast|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Gastric_cancer|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|not_specified": 2,
    "not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Familial_colorectal_cancer_type_X|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Mantle_cell_lymphoma|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Inherited_breast_cancer_and_ovarian_cancer|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Ataxia-telangiectasia_syndrome": 2,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_disorder|Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast|See_cases": 1,
    "Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_carcinoma|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Gastric_cancer": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|not_specified|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "not_provided|Ataxia-telangiectasia_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_disorder": 1,
    "Lung_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 4,
    "Diffuse_midline_glioma|_H3_K27-altered|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|not_provided|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|Gastric_cancer": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Gastric_cancer|Abnormal_central_motor_function|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast|not_provided": 1,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|T-cell_prolymphocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|ATM-related_disorder|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_urinary_bladder|Ataxia-telangiectasia_syndrome": 3,
    "Familial_cancer_of_breast|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Gastric_cancer|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|not_specified|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|T-cell_prolymphocytic_leukemia|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_provided": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 3,
    "Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "ATM-related_disorder|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Carcinoma_of_colon": 2,
    "not_provided|not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Triple-negative_breast_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Pancreatic_Cancer_Susceptibility_4|Breast_cancer|_susceptibility_to|Prostate_cancer_susceptibility|Ovarian_cancer|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Inherited_breast_cancer_and_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|ATM-related_cancer_predisposition|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_cancer|_familial_male": 1,
    "Ataxia-telangiectasia_syndrome|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Gastric_cancer|not_provided|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Neoplasm": 1,
    "Gastric_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Ataxia-telangiectasia_syndrome|Breast_carcinoma|Familial_cancer_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_specified": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "ATM-related_cancer_predisposition|Familial_colorectal_cancer_type_X|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Ataxia_-_telangiectasia_variant": 1,
    "Familial_colorectal_cancer_type_X|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "not_provided|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "Cancer_or_benign_tumor|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Breast_carcinoma": 1,
    "ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ATM-related_disorder|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Ataxia-telangiectasia_syndrome|Breast_cancer|_susceptibility_to|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 3,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "ATM-related_disorder|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Abnormal_central_motor_function|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Breast_carcinoma": 1,
    "Familial_cancer_of_breast|ATM-related_disorder|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Tip-toe_gait": 1,
    "ATM-related_cancer_predisposition|Gastric_cancer|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_pancreas|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast|C11orf65-related_disorder": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_pancreas": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "ATM-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia_telangiectasi|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 2,
    "ATM-related_cancer_predisposition|not_provided|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Abnormal_central_motor_function|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|CUP_(carcinoma_unknown_primary)_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ataxia_-_telangiectasia_variant|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Breast_cancer|_susceptibility_to": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Breast_neoplasm": 1,
    "ATM-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Colonic_neoplasm": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "C11orf65-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Carcinoma_of_colon|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|ATM-related_disorder|not_specified": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Familial_colorectal_cancer_type_X|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "ATM-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Abnormal_central_motor_function|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Childhood_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|not_provided|Familial_cancer_of_breast": 4,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Familial_colorectal_cancer_type_X": 1,
    "Malignant_tumor_of_breast|ATM-related_disorder|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Gastric_cancer|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Tip-toe_gait": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|not_specified": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Seizure|Cerebellar_ataxia|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "ATM-related_disorder|not_provided": 1,
    "Gastric_cancer|Breast_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|not_provided|not_specified": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|Familial_colorectal_cancer_type_X|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Familial_colorectal_cancer_type_X|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hepatoblastoma|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_specified|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_provided": 2,
    "Hereditary_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Mantle_cell_lymphoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Mantle_cell_lymphoma|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|NICE_approved_PARP_inhibitor_treatment|Inherited_breast_cancer_and_ovarian_cancer|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|T-cell_prolymphocytic_leukemia|Ataxia_-_telangiectasia_variant|Breast_cancer|_susceptibility_to": 1,
    "ATM-related_cancer_predisposition|not_specified": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|ATM-related_cancer_predisposition": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Tip-toe_gait|See_cases": 1,
    "ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_colorectal_cancer_type_X|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Breast_carcinoma|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Abnormal_central_motor_function|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X|Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Familial_ovarian_cancer|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided": 2,
    "Astroblastoma|_MN1-altered|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Carcinoma_of_colon|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "ATM-related_disorder|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|not_specified|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Intellectual_disability": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|ATM-related_disorder|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon": 1,
    "ATM-related_disorder|Colorectal_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Tip-toe_gait": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Familial_cancer_of_breast|T-cell_prolymphocytic_leukemia|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_thyroid_gland|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Gastric_cancer|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|ATM-related_disorder": 1,
    "Gastric_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X|not_provided": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Intellectual_disability|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|not_specified|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|ATM-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Tip-toe_gait|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|See_cases": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Tip-toe_gait": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Familial_pancreatic_carcinoma|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Abnormal_central_motor_function|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Ataxia-telangiectasia_without_immunodeficiency": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia_-_telangiectasia_variant|Ataxia-telangiectasia_syndrome": 1,
    "Malignant_tumor_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Abnormal_central_motor_function|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_colorectal_cancer_type_X|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Gastric_cancer|Breast_and/or_ovarian_cancer|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Uterine_corpus_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Tip-toe_gait|Breast_carcinoma": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Astrocytoma_IDH-mutant|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "ATM-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast|ATM-related_disorder|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "ATM-related_cancer_predisposition|Familial_ovarian_cancer|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|ATM-related_cancer_predisposition": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|ATM-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "ATM-related_cancer_predisposition|Gastric_cancer|ATM-related_disorder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Endometrial_carcinoma|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Breast_cancer|_susceptibility_to": 1,
    "ATM-related_disorder|Breast_cancer|_susceptibility_to|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Carcinoma_of_colon|Familial_cancer_of_breast": 1,
    "Familial_colorectal_cancer_type_X|not_provided|Ataxia-telangiectasia_syndrome|not_specified|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia_-_telangiectasia_variant|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_cancer_predisposition|Abnormal_central_motor_function|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Glioblastoma|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|Breast_cancer|_susceptibility_to|Familial_cancer_of_breast|not_provided|Tip-toe_gait": 1,
    "not_provided|Familial_cancer_of_breast|ATM-related_cancer_predisposition|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ataxia-telangiectasia_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|Astrocytoma_IDH-mutant|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Papillary_thyroid_carcinoma|Carcinoma_of_colon": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Multifocal_breast_carcinoma|Ataxia-telangiectasia_syndrome|Breast_carcinoma": 1,
    "Carcinoma_of_pancreas|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer": 1,
    "Ataxia-telangiectasia_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Papillary_renal_cell_carcinoma_type_1|Familial_cancer_of_breast": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|ATM-related_disorder|Familial_cancer_of_breast": 1,
    "Familial_colorectal_cancer_type_X|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_cancer|_early-onset|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Gait_ataxia": 1,
    "ATM-related_cancer_predisposition|Malignant_glioma|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Ataxia-telangiectasia_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Ovarian_cancer|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Inherited_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_provided|not_specified": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|ATM-related_disorder": 1,
    "ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Ataxia-telangiectasia_syndrome|not_provided": 1,
    "Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_cancer|_susceptibility_to": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Koolen-de_Vries_syndrome|Breast_cancer|_susceptibility_to": 1,
    "Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Familial_ovarian_cancer|ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Breast_cancer|_susceptibility_to|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "ATM-related_cancer_predisposition|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "ATM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Clear_cell_carcinoma_of_kidney|not_provided|Ataxia-telangiectasia_syndrome": 1,
    "ATM-related_cancer_predisposition|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "ATM-related_disorder|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|not_provided|not_specified|ATM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|not_provided|See_cases": 1,
    "Ataxia-telangiectasia_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_breast|ATM-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Ataxia-telangiectasia_syndrome|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_urinary_bladder|Gastric_cancer|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|ATM-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome|Malignant_tumor_of_urinary_bladder|Ataxia-telangiectasia_without_immunodeficiency": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Ataxia-telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome|Colorectal_polyposis": 1,
    "Ataxia-telangiectasia_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "ATM-related_disorder|Malignant_tumor_of_urinary_bladder|Ataxia-telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Familial_cancer_of_breast|Ataxia-telangiectasia_syndrome": 1,
    "Familial_cancer_of_breast|Carcinoma_of_colon|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Ataxia-telangiectasia_syndrome": 1,
    "not_provided|Epidermolysis_bullosa_simplex_4|_localized_or_generalized_intermediate|_autosomal_recessive": 5,
    "not_provided|EXPH5-related_disorder": 14,
    "EXPH5-related_disorder|not_provided": 12,
    "not_provided|EXPH5-related_disorder|Inborn_genetic_diseases": 1,
    "Epidermolysis_bullosa_simplex_4|_localized_or_generalized_intermediate|_autosomal_recessive|not_provided": 2,
    "Epidermolysis_bullosa_simplex_4|_localized_or_generalized_intermediate|_autosomal_recessive": 13,
    "EXPH5-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|EXPH5-related_disorder": 2,
    "EXPH5-related_disorder": 8,
    "EXPH5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DDX10-related_disorder|not_provided": 2,
    "DDX10-related_disorder": 9,
    "not_specified|not_provided|DDX10-related_disorder": 1,
    "DDX10-related_disorder|not_specified": 1,
    "X-linked_Alport_syndrome": 702,
    "RDX-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_24": 83,
    "Autosomal_recessive_nonsyndromic_hearing_loss_24|not_provided": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_24": 2,
    "RDX-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_24|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_24|RDX-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_24": 2,
    "RDX-related_disorder|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_24": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_24|Rare_genetic_deafness": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_24": 1,
    "not_provided|RDX-related_disorder": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_24|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_24|not_specified|not_provided": 1,
    "not_specified|RDX-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hearing_loss|_autosomal_recessive": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_24|Hearing_loss|_autosomal_recessive": 1,
    "Oocyte_maturation_defect_8": 5,
    "PPP2R1B-related_disorder": 6,
    "not_provided|PPP2R1B-related_disorder": 1,
    "ALG9_congenital_disorder_of_glycosylation": 427,
    "not_provided|ALG9_congenital_disorder_of_glycosylation": 39,
    "ALG9_congenital_disorder_of_glycosylation|not_provided": 21,
    "ALG9-related_disorder": 11,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome": 2,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|ALG9-related_disorder": 3,
    "ALG9-associated_autosomal_dominant_polycystic_kidney_disease|ALG9_congenital_disorder_of_glycosylation|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome": 50,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases|ALG9-related_disorder": 1,
    "Congenital_disorder_of_glycosylation|ALG9_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|ALG9_congenital_disorder_of_glycosylation": 2,
    "ALG9_congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|ALG9-related_disorder": 7,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|ALG9-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome": 1,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|ALG9-related_disorder|not_specified": 1,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|ALG9-associated_autosomal_dominant_polycystic_kidney_disease": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_specified": 7,
    "ALG9_congenital_disorder_of_glycosylation|ALG9-related_disorder|Gillessen-Kaesbach-Nishimura_syndrome": 1,
    "ALG9-associated_autosomal_dominant_polycystic_kidney_disease|not_provided": 1,
    "Gillessen-Kaesbach-Nishimura_syndrome|not_provided|Gillessen-Kaesbach-Nishimura_dysplasia": 1,
    "Inborn_genetic_diseases|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome": 1,
    "not_specified|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_liver_disease": 1,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|not_specified": 1,
    "Autosomal_dominant_polycystic_liver_disease|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|Inborn_genetic_diseases": 1,
    "ALG9-related_disorder|ALG9_congenital_disorder_of_glycosylation|not_specified": 2,
    "not_specified|not_provided|ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome": 1,
    "Gillessen-Kaesbach-Nishimura_syndrome|ALG9_congenital_disorder_of_glycosylation|ALG9-related_disorder": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_specified|not_provided|ALG9-related_disorder": 1,
    "ALG9-related_disorder|ALG9_congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|not_specified|not_provided": 1,
    "Gillessen-Kaesbach-Nishimura_syndrome|ALG9_congenital_disorder_of_glycosylation": 2,
    "not_provided|ALG9-related_disorder|ALG9_congenital_disorder_of_glycosylation|not_specified|Gillessen-Kaesbach-Nishimura_syndrome": 1,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|Autosomal_dominant_polycystic_liver_disease|not_provided|See_cases": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Gillessen-Kaesbach-Nishimura_syndrome|ALG9-related_disorder": 1,
    "not_specified|ALG9_congenital_disorder_of_glycosylation|ALG9-related_disorder|Gillessen-Kaesbach-Nishimura_syndrome|not_provided": 1,
    "not_provided|not_specified|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9-related_disorder|not_specified|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|Gillessen-Kaesbach-Nishimura_syndrome|ALG9-related_disorder|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 7,
    "Familial_cystic_renal_disease|not_provided|not_specified": 1,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|not_specified": 2,
    "Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_Myopathy|_Dominant": 1,
    "Cataract_16_multiple_types|Myofibrillar_myopathy_2|Fatal_infantile_hypertonic_myofibrillar_myopathy": 2,
    "Posterior_polar_cataract|Myofibrillar_myopathy_2|Myofibrillar_Myopathy|_Dominant": 1,
    "Fatal_infantile_hypertonic_myofibrillar_myopathy|Cataract_16_multiple_types|Myofibrillar_myopathy_2": 1,
    "Cataract_16_multiple_types": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II": 20,
    "Dilated_cardiomyopathy_1II": 116,
    "Myofibrillar_myopathy_2|CRYAB-related_disorder": 1,
    "Dilated_cardiomyopathy_1II|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myofibrillar_myopathy_2": 4,
    "Dilated_cardiomyopathy_1II|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1II|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1II|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|not_provided": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1II|Cardiovascular_phenotype": 14,
    "Fatal_infantile_hypertonic_myofibrillar_myopathy|Hypertrophic_cardiomyopathy|not_provided|Cataract_16_multiple_types|Myofibrillar_myopathy_2": 1,
    "Dilated_cardiomyopathy_1II|not_provided": 7,
    "Dilated_cardiomyopathy_1II|not_specified": 3,
    "Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_myopathy_2|Dilated_cardiomyopathy_1II|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1II|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Congestive_heart_failure|Myofibrillar_Myopathy|_Dominant|CRYAB-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1II|not_provided|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cardiomyopathy|Cataract_16_multiple_types|Primary_familial_hypertrophic_cardiomyopathy|Developmental_cataract": 1,
    "Myofibrillar_myopathy_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|not_provided|Cardiomyopathy": 1,
    "Myofibrillar_Myopathy|_Dominant|Dilated_cardiomyopathy_1II|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1II": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cataract_16_multiple_types": 1,
    "Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cataract_16_multiple_types|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|not_specified": 3,
    "Dilated_cardiomyopathy_1II|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_myopathy_2|Cataract_16_multiple_types|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1II|Cardiovascular_phenotype|not_provided": 5,
    "Fatal_infantile_hypertonic_myofibrillar_myopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1II": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1II|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cataract_16_multiple_types|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1II": 1,
    "Myofibrillar_myopathy_2|Cataract_16_multiple_types|Myofibrillar_Myopathy|_Dominant|Cardiovascular_phenotype|Fatal_infantile_hypertonic_myofibrillar_myopathy|not_specified|Dilated_cardiomyopathy_1II|not_provided": 1,
    "Dilated_cardiomyopathy_1II|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1II|not_provided|Developmental_cataract": 1,
    "not_specified|Dilated_cardiomyopathy_1II|Cardiovascular_phenotype|not_provided|Myofibrillar_myopathy_2|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy": 1,
    "Dilated_cardiomyopathy_1II|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_myopathy_2|not_provided": 1,
    "Cardiovascular_phenotype|Xeroderma_pigmentosum|_group_D|not_specified|Dilated_cardiomyopathy_1II": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1II": 3,
    "not_specified|Dilated_cardiomyopathy_1II": 1,
    "CRYAB-related_disorder|Dilated_cardiomyopathy_1II|Cardiovascular_phenotype": 1,
    "Myofibrillar_myopathy_2|Cataract_16_multiple_types|Cardiovascular_phenotype|Dilated_cardiomyopathy_1II": 1,
    "Fatal_infantile_hypertonic_myofibrillar_myopathy|not_specified|Dilated_cardiomyopathy_1II|Myofibrillar_Myopathy|_Dominant|Cardiovascular_phenotype|not_provided|Cataract_16_multiple_types": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|CRYAB-related_disorder|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2|not_specified": 1,
    "Cataract_16_multiple_types|Dilated_cardiomyopathy_1II|not_provided|CRYAB-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1II": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_myopathy_2|Cataract_16_multiple_types": 1,
    "Cardiovascular_phenotype|Myofibrillar_myopathy_2|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Dilated_cardiomyopathy_1II|not_provided|not_specified": 1,
    "Fatal_infantile_hypertonic_myofibrillar_myopathy|Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2|Cataract_16_multiple_types|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1II|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_myopathy_2|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1II|Fatal_infantile_hypertonic_myofibrillar_myopathy|Myofibrillar_myopathy_2|Cataract_16_multiple_types|Myofibrillar_Myopathy|_Dominant": 1,
    "CRYAB-related_disorder": 1,
    "Cataract_16_multiple_types|not_provided|Dilated_cardiomyopathy_1II|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1II|Myofibrillar_myopathy_2|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1II|not_provided|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cataract_16_multiple_types|Myofibrillar_myopathy_2|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1II|Cardiovascular_phenotype|Myofibrillar_myopathy_2": 1,
    "Myofibrillar_myopathy_2|Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|Dilated_cardiomyopathy_1II|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1II": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1II|Cataract_16_multiple_types|not_provided": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1II": 1,
    "Dilated_cardiomyopathy_1II|not_provided|Myofibrillar_myopathy_2|Fatal_infantile_hypertonic_myofibrillar_myopathy|Cataract_16_multiple_types|Cardiovascular_phenotype": 1,
    "Cataract_16_multiple_types|Myofibrillar_myopathy_2|Fatal_infantile_hypertonic_myofibrillar_myopathy|Dilated_cardiomyopathy_1II|not_provided": 1,
    "Dilated_cardiomyopathy_1II|Cataract_16_multiple_types|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1II|Cataract_16_multiple_types|Cardiomyopathy": 1,
    "Cataract_16_multiple_types|Fatal_infantile_hypertonic_myofibrillar_myopathy|not_specified|Myofibrillar_Myopathy|_Dominant": 1,
    "Pyruvate_dehydrogenase_E2_deficiency": 139,
    "not_specified|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "DLAT-related_disorder|not_specified|not_provided|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "not_provided|Pyruvate_dehydrogenase_E2_deficiency": 12,
    "Pyruvate_dehydrogenase_E2_deficiency|not_provided|not_specified": 2,
    "Pyruvate_dehydrogenase_E2_deficiency|not_provided": 10,
    "Pyruvate_dehydrogenase_E2_deficiency|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|Pyruvate_dehydrogenase_E2_deficiency|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E2_deficiency": 2,
    "Pyruvate_dehydrogenase_E2_deficiency|not_specified": 8,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E2_deficiency": 9,
    "Pyruvate_dehydrogenase_E2_deficiency|DLAT-related_disorder": 2,
    "not_provided|Pyruvate_dehydrogenase_E2_deficiency|Inborn_genetic_diseases": 3,
    "not_specified|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "Pyruvate_dehydrogenase_E2_deficiency|not_specified|not_provided": 5,
    "not_specified|not_provided|Pyruvate_dehydrogenase_E2_deficiency": 4,
    "not_provided|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E2_deficiency": 2,
    "not_provided|Pyruvate_dehydrogenase_E2_deficiency|not_specified": 1,
    "not_specified|Pyruvate_dehydrogenase_E2_deficiency|not_provided": 1,
    "not_provided|DLAT-related_disorder|not_specified|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "DLAT-related_disorder|Pyruvate_dehydrogenase_E2_deficiency|not_provided": 1,
    "Leigh_syndrome|not_provided|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "not_provided|DLAT-related_disorder|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "DLAT-related_disorder": 1,
    "DLAT-related_disorder|Pyruvate_dehydrogenase_E2_deficiency": 1,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E2_deficiency|Leigh_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Cowden_syndrome": 1,
    "SDHD-related_disorder": 6,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 5,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3": 14,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 8,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 4,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 56,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 6,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3": 9,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 5,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 12,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1": 7,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome": 24,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3": 6,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 2,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss": 5,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Pheochromocytoma/paraganglioma_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 3,
    "Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 7,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 30,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss": 3,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma": 4,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome": 11,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Pheochromocytoma/paraganglioma_syndrome_1": 28,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss": 16,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3|SDHD-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3": 10,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 3,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma": 15,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma": 5,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma": 2,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|SDHD-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 3,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome": 5,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|not_provided": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma": 4,
    "Pheochromocytoma/paraganglioma_syndrome_1|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome": 4,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 7,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma": 6,
    "Hereditary_cancer-predisposing_syndrome|not_specified|SDHD-related_disorder|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome": 3,
    "Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 11,
    "Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|not_provided": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma": 2,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|SDHD-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma": 5,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|not_provided": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|not_provided": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 7,
    "Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 3,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_pheochromocytoma-paraganglioma|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 4,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss": 2,
    "SDHD-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 4,
    "Pheochromocytoma/paraganglioma_syndrome_1|Carney-Stratakis_syndrome|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 2,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome": 2,
    "not_provided|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 6,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome": 1,
    "Pheochromocytoma|Paraganglioma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "not_provided|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|SDHD-related_disorder|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Carcinoid_tumor_of_intestine": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 7,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_3|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Pheochromocytoma/paraganglioma_syndrome_1|not_provided|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 2,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3": 2,
    "not_provided|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|SDHD-related_disorder|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome": 3,
    "Pheochromocytoma/paraganglioma_syndrome_1|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|SDHD-related_disorder|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|not_provided|Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|not_specified|not_provided": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Microcephaly|not_provided|Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome": 1,
    "Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_4|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Fatal_infantile_mitochondrial_cardiomyopathy|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|not_provided": 1,
    "SDHD-related_disorder|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|not_provided": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Mitochondrial_complex_2_deficiency|_nuclear_type_3|not_provided|SDHD-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|not_provided|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma": 1,
    "Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_3": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|not_specified": 1,
    "SDHD-related_disorder|not_specified|not_provided": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_3|not_specified|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "SDHD-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Carney-Stratakis_syndrome|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|SDHD-related_disorder|Pheochromocytoma/paraganglioma_syndrome_1|not_provided": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|not_provided": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|not_provided": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_pheochromocytoma-paraganglioma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|SDHD-related_disorder|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3": 1,
    "Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|not_provided": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "not_provided|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 2,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|SDHD-related_disorder|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Carney-Stratakis_syndrome|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3": 1,
    "Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Pheochromocytoma|Cowden_syndrome_3|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Hereditary_cancer-predisposing_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1|Mitochondrial_complex_2_deficiency|_nuclear_type_3": 1,
    "Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma/paraganglioma_syndrome_1|not_specified|Hereditary_pheochromocytoma-paraganglioma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|not_provided": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Cowden_syndrome_3|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Carney-Stratakis_syndrome|Cowden_syndrome_3|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma/paraganglioma_syndrome_1": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Cowden_syndrome_3|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_provided": 1,
    "Cowden_syndrome_3|Carney-Stratakis_syndrome|Paragangliomas_with_sensorineural_hearing_loss|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|Pheochromocytoma/paraganglioma_syndrome_1|Carney-Stratakis_syndrome|Cowden_syndrome_3": 1,
    "Cowden_syndrome_3|Pheochromocytoma|Paragangliomas_with_sensorineural_hearing_loss|Carney-Stratakis_syndrome|Mitochondrial_complex_2_deficiency|_nuclear_type_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Paragangliomas_with_sensorineural_hearing_loss|Cowden_syndrome_3|Pheochromocytoma|Carney-Stratakis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma": 1,
    "SDHD-related_disorder|Cowden_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Pheochromocytoma/paraganglioma_syndrome_1|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|not_specified|not_provided": 1,
    "not_specified|not_provided|Pheochromocytoma": 1,
    "not_provided|not_specified|Pheochromocytoma": 1,
    "HIGH_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_6": 8,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 239,
    "not_provided|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 15,
    "Hyperphenylalaninemia|_bh4-deficient|_a|_due_to_partial_pts_deficiency|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "not_provided|PTS-related_disorder|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia": 7,
    "not_specified|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 3,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Inborn_genetic_diseases": 4,
    "Hyperphenylalaninemia|_bh4-deficient|_a|_due_to_partial_pts_deficiency": 2,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|not_provided": 7,
    "PTS-related_disorder|not_provided|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "PTS-related_disorder": 5,
    "PTS-related_disorder|not_provided": 1,
    "PTS-related_disorder|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 2,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|PTS-related_disorder": 2,
    "GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|Hyperphenylalaninemia_due_to_tetrahydrobiopterin_deficiency|not_provided|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Noonan_syndrome_1|not_specified": 1,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|not_specified": 1,
    "not_specified|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Hyperphenylalaninemia|_bh4-deficient|_a|_due_to_partial_pts_deficiency": 1,
    "Inborn_genetic_diseases|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|PTS-related_disorder|not_specified|not_provided": 1,
    "TTC12-related_disorder": 6,
    "Ciliary_dyskinesia|_primary|_45|not_provided": 3,
    "TTC12-related_disorder|not_provided": 1,
    "Ciliary_dyskinesia|_primary|_45|TTC12-related_disorder": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_45": 1,
    "not_provided|TTC12-related_disorder": 1,
    "ANKK1-related_disorder": 16,
    "not_provided|ANKK1-related_disorder": 3,
    "ANKK1-related_disorder|not_provided": 1,
    "ANKK1-related_disorder|not_specified|not_provided|Schizophrenia|Taq1A_POLYMORPHISM": 1,
    "Dystonic_disorder|not_specified|not_provided": 2,
    "not_provided|Dystonic_disorder|not_specified": 1,
    "Schizophrenia|not_specified|Dystonic_disorder|not_provided": 1,
    "DRD2-associated_Dystonia|Dystonic_disorder|not_specified|not_provided": 1,
    "Dystonic_disorder|not_provided|not_specified": 2,
    "TMPRSS5-related_disorder": 4,
    "TMPRSS5-related_disorder|not_specified|not_provided": 1,
    "not_provided|TMPRSS5-related_disorder|not_specified": 1,
    "ZBTB16-related_disorder": 6,
    "ZBTB16-related_disorder|not_provided": 1,
    "Skeletal_defects|_genital_hypoplasia|_and_intellectual_disability": 1,
    "Achalasia-progeroid_syndrome": 1,
    "not_specified|Gait_ataxia": 1,
    "Growth_restriction|_hypoplastic_kidneys|_alopecia|_and_distinctive_facies": 3,
    "not_provided|Hypertriglyceridemia_1": 2,
    "Familial_type_5_hyperlipoproteinemia|Hypertriglyceridemia_1": 1,
    "Hypertriglyceridemia_1": 3,
    "Cardiovascular_phenotype|Hypertriglyceridemia_1|Familial_type_5_hyperlipoproteinemia|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|APOA5-related_disorder": 1,
    "not_provided|APOA5-related_disorder": 1,
    "Cardiovascular_phenotype|Familial_type_5_hyperlipoproteinemia|Hypertriglyceridemia_1|not_provided": 1,
    "APOA5-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Familial_type_5_hyperlipoproteinemia|Hypertriglyceridemia_1": 1,
    "Dementia": 1,
    "Familial_type_5_hyperlipoproteinemia": 4,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertriglyceridemia_1": 1,
    "APOA5-related_disorder|Hyperlipoproteinemia|_type_I": 1,
    "APOA5-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Familial_type_5_hyperlipoproteinemia|Cardiovascular_phenotype": 1,
    "Hypertriglyceridemia|Cardiovascular_phenotype|not_provided|Hypertriglyceridemia_1|Familial_type_5_hyperlipoproteinemia": 1,
    "Cardiovascular_phenotype|not_provided|APOA5-related_disorder": 2,
    "APOA5-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hypertriglyceridemia_1|Familial_type_5_hyperlipoproteinemia|not_provided|not_specified": 1,
    "Familial_type_5_hyperlipoproteinemia|not_provided": 1,
    "not_provided|APOLIPOPROTEIN_A-IV_RARE_VARIANT|_APOA4*0": 1,
    "not_provided|APOLIPOPROTEIN_A-IV_POLYMORPHISM|_APOA4*1/APOA4*2": 1,
    "not_provided|APOA4-related_disorder": 3,
    "APOA4-related_disorder|not_provided": 3,
    "not_provided|APOLIPOPROTEIN_A-IV_RARE_VARIANT|_APOA4*3": 1,
    "APOA4-related_disorder": 3,
    "Tubulointerstitial_kidney_disease|_autosomal_dominant_6": 2,
    "High_density_lipoprotein_deficiency|_Detroit_type|.": 1,
    "Cardiovascular_phenotype|Coronary_heart_disease|not_specified|not_provided|Apolipoprotein_c-III_deficiency|Cholesterol-ester_transfer_protein_deficiency": 1,
    "Apolipoprotein_c-III_deficiency|Cardiovascular_phenotype|Coronary_heart_disease|not_specified|not_provided": 1,
    "Apolipoprotein_c-III_deficiency|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|APOC3-related_disorder|not_provided": 1,
    "Apolipoprotein_c-III_deficiency|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Coronary_heart_disease|not_provided|not_specified|Apolipoprotein_c-III_deficiency": 1,
    "Apolipoprotein_c-III_deficiency": 3,
    "Apolipoprotein_c-III_deficiency|not_specified|Coronary_heart_disease|not_provided": 1,
    "Apolipoprotein_C-III|_nonglycosylated": 1,
    "Myocardial_infarction|_susceptibility_to|not_specified|not_provided": 1,
    "not_specified|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1|Hypoalphalipoproteinemia|_primary|_2": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1": 6,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|not_provided": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type": 1,
    "Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 16,
    "Cardiovascular_phenotype|not_specified|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Hypoalphalipoproteinemia|_primary|_1|not_specified|Hypoalphalipoproteinemia|_primary|_2": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_provided|Cardiovascular_phenotype": 1,
    "Hypoalphalipoproteinemia|_primary|_2": 8,
    "Hypoalphalipoproteinemia|_primary|_2|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|not_provided|APOLIPOPROTEIN_A-I_(MUNSTER4)": 1,
    "not_provided|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type": 1,
    "not_provided|Cardiovascular_phenotype|APOA1-related_disorder": 1,
    "Familial_amyloid_polyneuropathy|_Iowa_type": 7,
    "APOLIPOPROTEIN_A-I_(MILANO)": 1,
    "not_provided|Apolipoprotein_A-I_deficiency": 1,
    "not_provided|Familial_visceral_amyloidosis|_Ostertag_type|not_specified|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Cardiovascular_phenotype": 1,
    "APOA1-related_disorder|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 1,
    "Hypoalphalipoproteinemia|_primary|_1|not_specified|Cardiovascular_phenotype|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "not_provided|Hypoalphalipoproteinemia|_primary|_2|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Cardiovascular_phenotype": 1,
    "APOA1-related_disorder|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_provided|Cardiovascular_phenotype": 1,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate|Hypoalphalipoproteinemia|_primary|_2|Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 2,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 1,
    "not_provided|APOLIPOPROTEIN_A-I_(GIESSEN)": 1,
    "Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Hypoalphalipoproteinemia|_primary|_2|Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_1|Familial_visceral_amyloidosis|_Ostertag_type": 2,
    "Cardiovascular_phenotype|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate": 1,
    "APOLIPOPROTEIN_A-I_(NORWAY)": 1,
    "Cardiovascular_phenotype|Familial_High_Density_Lipoprotein_Deficiency|Familial_visceral_amyloidosis|_Ostertag_type|not_provided": 1,
    "Chronic_kidney_disease|Cardiovascular_phenotype|not_specified|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|not_provided": 1,
    "APOLIPOPROTEIN_A-I_(MARBURG)": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|not_provided": 1,
    "APOA1-related_disorder|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_provided": 1,
    "APOA1-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2": 1,
    "not_specified|Cardiovascular_phenotype|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Familial_amyloid_polyneuropathy|_Iowa_type": 1,
    "not_specified|not_provided|APOA1-related_disorder": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1|not_specified|Hypoalphalipoproteinemia|_primary|_2": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Cardiovascular_phenotype|not_specified|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Cardiovascular_phenotype|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1|not_provided|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 1,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "APOA1-related_disorder|not_specified|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|Cardiovascular_phenotype|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Cardiovascular_phenotype|not_provided|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|APOLIPOPROTEIN_A-I_(BALTIMORE)|not_provided": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type": 1,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type|not_specified|not_provided|APOLIPOPROTEIN_A-I_(MUNSTER3B)": 1,
    "APOLIPOPROTEIN_A-I_(MUNSTER3C)": 1,
    "Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|_intermediate|not_specified|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|not_provided|Hypoalphalipoproteinemia|_primary|_2": 1,
    "not_provided|Cardiovascular_phenotype|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_amyloid_polyneuropathy|_Iowa_type": 1,
    "Hypoalphalipoproteinemia|_primary|_1|Cardiovascular_phenotype|not_specified|Familial_amyloid_polyneuropathy|_Iowa_type|Hypoalphalipoproteinemia|_primary|_2|Hypoalphalipoproteinemia|_primary|_2|_intermediate|Familial_visceral_amyloidosis|_Ostertag_type|not_provided": 1,
    "Hypoalphalipoproteinemia|_primary|_2|Cardiovascular_phenotype|not_provided|Familial_visceral_amyloidosis|_Ostertag_type|Hypoalphalipoproteinemia|_primary|_1|Hypoalphalipoproteinemia|_primary|_2|_intermediate": 1,
    "SIK3-related_disorder|not_provided": 2,
    "SIK3-related_disorder": 12,
    "SIK3-related_disorder|Spondyloepimetaphyseal_dysplasia|_Krakow_type|not_provided": 2,
    "not_specified|not_provided|SIK3-related_disorder": 1,
    "not_provided|SIK3-related_disorder": 2,
    "not_specified|SIK3-related_disorder": 1,
    "Spondyloepimetaphyseal_dysplasia|_Krakow_type|not_provided": 3,
    "Spondyloepimetaphyseal_dysplasia|_Krakow_type": 2,
    "Midline_facial_cleft|Pericallosal_lipoma|Skin_tags|not_provided": 1,
    "Skin_tags|Preauricular_skin_tag|Pericallosal_lipoma|not_provided": 1,
    "CEP164-related_disorder": 21,
    "not_provided|Nephronophthisis_15": 14,
    "Nephronophthisis_15": 1070,
    "Inborn_genetic_diseases|Nephronophthisis_15": 45,
    "CEP164-related_disorder|Nephronophthisis_15|Inborn_genetic_diseases": 4,
    "Nephronophthisis_15|Inborn_genetic_diseases": 39,
    "not_specified|not_provided|Nephronophthisis_15": 4,
    "CEP164-related_disorder|Nephronophthisis_15": 39,
    "Nephronophthisis_15|CEP164-related_disorder": 28,
    "Nephronophthisis_15|not_provided": 13,
    "Inborn_genetic_diseases|CEP164-related_disorder|Nephronophthisis_15": 5,
    "Nephronophthisis_15|CEP164-related_disorder|Inborn_genetic_diseases": 4,
    "not_provided|not_specified|Nephronophthisis_15": 2,
    "Nephronophthisis_15|CEP164-related_disorder|not_provided": 7,
    "Nephronophthisis_15|not_provided|Retinal_dystrophy": 1,
    "not_provided|Nephronophthisis_15|CEP164-related_disorder": 3,
    "CEP164-related_disorder|not_provided|Nephronophthisis_15": 2,
    "Nephronophthisis_15|not_provided|Inborn_genetic_diseases|CEP164-related_disorder|Retinal_dystrophy": 1,
    "Nephronophthisis_15|Renal_dysplasia_and_retinal_aplasia": 1,
    "CEP164-related_disorder|Nephronophthisis_15|not_provided": 2,
    "Inborn_genetic_diseases|CEP164-related_disorder|not_provided|Nephronophthisis_15": 1,
    "Nephronophthisis_15|CEP164-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Nephronophthisis_15|Inborn_genetic_diseases": 3,
    "Nephronophthisis_15|CEP164-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Nephronophthisis_15|not_specified": 6,
    "not_provided|Nephronophthisis_15|not_specified": 4,
    "CEP164-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis_15|not_specified|not_provided": 5,
    "Nephronophthisis_15|Inborn_genetic_diseases|CEP164-related_disorder|not_provided": 2,
    "Nephronophthisis_15|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_specified|not_provided|Nephronophthisis_15|CEP164-related_disorder": 1,
    "CEP164-related_disorder|Inborn_genetic_diseases|Nephronophthisis_15": 4,
    "not_provided|CEP164-related_disorder|Nephronophthisis_15": 1,
    "Nephronophthisis_15|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephronophthisis_15|CEP164-related_disorder": 9,
    "not_specified|Nephronophthisis_15": 2,
    "Nephronophthisis_15|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Nephronophthisis_15|not_provided|CEP164-related_disorder": 1,
    "Retinal_dystrophy|Nephronophthisis_15": 1,
    "not_specified|Inborn_genetic_diseases|Nephronophthisis_15|CEP164-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Nephronophthisis_15": 1,
    "Inborn_genetic_diseases|not_specified|CEP164-related_disorder|not_provided|Nephronophthisis_15": 1,
    "Retinal_dystrophy|not_specified|not_provided|CEP164-related_disorder|Nephronophthisis_15": 2,
    "CEP164-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Nephronophthisis_15": 1,
    "not_specified|Nephronophthisis_15|not_provided": 1,
    "Nephronophthisis_15|CEP164-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Nephronophthisis_15|CEP164-related_disorder|not_specified": 2,
    "Retinal_dystrophy|Inborn_genetic_diseases|Nephronophthisis_15": 1,
    "Nephronophthisis_15|Inborn_genetic_diseases|not_provided": 1,
    "Nephronophthisis_15|not_provided|not_specified": 1,
    "Nephronophthisis_15|Inborn_genetic_diseases|Nephronophthisis|CEP164-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis_15": 1,
    "DSCAML1-related_disorder": 6,
    "not_provided|DSCAML1-related_disorder": 25,
    "DSCAML1-related_disorder|not_provided": 25,
    "DSCAML1-related_disorder|not_provided|not_specified": 2,
    "not_specified|Marfanoid_habitus_and_intellectual_disability": 1,
    "Renal_hypomagnesemia_2": 13,
    "Renal_hypomagnesemia_2|not_provided": 10,
    "Renal_hypomagnesemia_2|not_specified|not_provided": 1,
    "FXYD2-related_disorder": 2,
    "not_provided|Renal_hypomagnesemia_2": 8,
    "not_provided|FXYD6-FXYD2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Renal_hypomagnesemia_2": 1,
    "not_specified|not_provided|FXYD2-related_disorder|Renal_hypomagnesemia_2|Inborn_genetic_diseases": 1,
    "FXYD2-related_disorder|not_provided": 1,
    "Renal_hypomagnesemia_2|not_provided|FXYD2-related_disorder": 1,
    "not_provided|FXYD2-related_disorder": 1,
    "Renal_Hypomagnesemia|_Dominant|not_provided": 1,
    "Inflammatory_bowel_disease_28": 338,
    "not_provided|Inflammatory_bowel_disease_28": 26,
    "not_specified|Inflammatory_bowel_disease_28|not_provided": 2,
    "Inflammatory_bowel_disease_28|Inborn_genetic_diseases": 13,
    "IL10RA-related_disorder": 1,
    "Inflammatory_bowel_disease_28|not_specified|not_provided": 2,
    "Inflammatory_bowel_disease_28|not_provided": 13,
    "not_provided|Inflammatory_bowel_disease_28|not_specified": 2,
    "Inborn_genetic_diseases|Inflammatory_bowel_disease_28": 12,
    "IL10RA-related_disorder|Inflammatory_bowel_disease_28": 4,
    "IL10RA-related_disorder|Inflammatory_bowel_disease_28|not_provided": 1,
    "not_provided|Inflammatory_bowel_disease_28|IL10RA-related_disorder": 2,
    "not_specified|not_provided|Inflammatory_bowel_disease_28": 1,
    "not_provided|Inborn_genetic_diseases|Inflammatory_bowel_disease_28": 1,
    "not_provided|not_specified|Inflammatory_bowel_disease_28": 1,
    "Inborn_genetic_diseases|not_provided|Inflammatory_bowel_disease_28|IL10RA-related_disorder": 1,
    "Inflammatory_bowel_disease_28|not_provided|not_specified": 1,
    "Inflammatory_bowel_disease_28|IL10RA-related_disorder": 2,
    "Inflammatory_bowel_disease_28|not_provided|IL10RA-related_disorder": 1,
    "Long_QT_syndrome_10|Congenital_long_QT_syndrome": 2,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_10": 3,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_10": 1,
    "Long_QT_syndrome_10": 70,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_10": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome_10": 24,
    "not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome_10": 1,
    "Long_QT_syndrome_10|Cardiovascular_phenotype": 20,
    "not_provided|Long_QT_syndrome_10|Cardiovascular_phenotype": 3,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_10": 3,
    "not_provided|Long_QT_syndrome_10|SUDDEN_INFANT_DEATH_SYNDROME|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome_10|SCN4B-related_disorder|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome_10|SCN4B-related_disorder|not_specified": 1,
    "Long_QT_syndrome_10|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Long_QT_syndrome_10": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_10|not_provided": 3,
    "Atrial_fibrillation|_familial|_17": 2,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_10": 1,
    "not_specified|Long_QT_syndrome_10|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_10|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome_10": 3,
    "not_provided|Long_QT_syndrome_10|Cardiovascular_phenotype|not_specified": 1,
    "Long_QT_syndrome_10|not_provided": 2,
    "Long_QT_syndrome_10|not_specified": 2,
    "Long_QT_syndrome_10|Cardiovascular_phenotype|not_specified|not_provided|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_10|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_10|SCN4B-related_disorder|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_10": 1,
    "Congenital_long_QT_syndrome|not_specified": 3,
    "Atrial_fibrillation|_familial|_14": 69,
    "Atrial_fibrillation|_familial|_14|Cardiovascular_phenotype": 19,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_14": 31,
    "Cardiovascular_phenotype|not_provided|Atrial_fibrillation|_familial|_14|Variant_of_unknown_significance": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_14": 4,
    "Cardiovascular_phenotype|not_provided|Atrial_fibrillation|_familial|_14": 3,
    "SCN2B-related_disorder|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_14": 1,
    "not_specified|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_14": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_14|not_provided": 5,
    "Atrial_fibrillation|_familial|_14|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Atrial_fibrillation|_familial|_14|not_provided": 1,
    "not_specified|Atrial_fibrillation|_familial|_14|Cardiovascular_phenotype": 2,
    "SCN2B-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Atrial_fibrillation|_familial|_14|not_provided": 1,
    "Atrial_fibrillation|_familial|_14|not_provided|Cardiovascular_phenotype": 1,
    "Atrial_fibrillation|_familial|_14|SCN2B-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Atrial_fibrillation|_familial|_14|not_specified": 1,
    "Atrial_fibrillation|_familial|_14|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Atrial_fibrillation|_familial|_14|Cardiovascular_phenotype": 1,
    "MPZL2-related_disorder": 9,
    "Inborn_genetic_diseases|MPZL2-related_disorder": 2,
    "Hearing_loss|_autosomal_recessive_111": 11,
    "MPZL2-related_disorder|Hearing_loss|_autosomal_recessive_111|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_111|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_111|Hearing_loss|_autosomal_recessive|MPZL2-related_disorder|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_111|MPZL2-related_disorder": 1,
    "Immunodeficiency_18": 215,
    "not_provided|Immunodeficiency_18": 6,
    "not_specified|Immunodeficiency_18": 1,
    "Immunodeficiency_18|not_specified": 4,
    "not_provided|Immunodeficiency_18|not_specified": 3,
    "Immunodeficiency_18|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|Immunodeficiency_18": 4,
    "Immunodeficiency_18|not_provided": 3,
    "Immunodeficiency_18|_severe_combined_immunodeficiency_variant": 1,
    "Immunodeficiency_18|not_provided|Inborn_genetic_diseases": 1,
    "Immunodeficiency_18|Severe_combined_immunodeficiency_disease": 1,
    "CD3E-related_disorder|Immunodeficiency_18|not_provided": 1,
    "CD3E-related_disorder|Severe_combined_immunodeficiency_disease|not_provided|Immunodeficiency_18": 1,
    "Severe_combined_immunodeficiency_disease|not_provided|Immunodeficiency_18": 1,
    "CD3E-related_disorder": 1,
    "not_specified|not_provided|Severe_combined_immunodeficiency_disease": 1,
    "Immunodeficiency_19": 169,
    "not_specified|Immunodeficiency_19": 2,
    "Immunodeficiency_19|Inborn_genetic_diseases": 4,
    "not_specified|Immunodeficiency_104|Immunodeficiency_19|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|Immunodeficiency_19": 1,
    "Immunodeficiency_19|not_provided|Inborn_genetic_diseases": 1,
    "Immunodeficiency_19|not_specified": 3,
    "not_specified|Immunodeficiency_19|not_provided": 1,
    "Immunodeficiency_19|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency_19": 5,
    "not_provided|Immunodeficiency_19": 2,
    "CD3D-related_disorder|Immunodeficiency_19": 1,
    "Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|Immunodeficiency_due_to_defect_in_CD3-gamma": 1,
    "Combined_immunodeficiency_due_to_CD3gamma_deficiency|not_provided": 7,
    "Combined_immunodeficiency_due_to_CD3gamma_deficiency": 124,
    "CD3G-related_disorder|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 1,
    "CD3G-related_disorder|not_provided|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 2,
    "not_specified|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 3,
    "Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 2,
    "Combined_immunodeficiency_due_to_CD3gamma_deficiency|not_specified": 3,
    "Immunodeficiency_due_to_defect_in_CD3-gamma|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 1,
    "not_provided|not_specified|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 1,
    "not_provided|Combined_immunodeficiency_due_to_CD3gamma_deficiency": 1,
    "Immunodeficiency_due_to_defect_in_CD3-gamma|not_provided": 1,
    "Immunodeficiency_due_to_defect_in_CD3-gamma": 1,
    "Inborn_genetic_diseases|not_provided|UBE4A-related_disorder": 1,
    "UBE4A-related_disorder": 4,
    "Neurodevelopmental_disorder_with_hypotonia_and_gross_motor_and_speech_delay|not_provided": 1,
    "not_specified|Neurodevelopmental_disorder_with_hypotonia_and_gross_motor_and_speech_delay": 1,
    "Retinitis_pigmentosa_11": 40,
    "KMT2A-related_disorder": 29,
    "not_provided|Wiedemann-Steiner_syndrome": 44,
    "not_provided|Wiedemann-Steiner_syndrome|not_specified": 2,
    "Wiedemann-Steiner_syndrome|not_provided|KMT2A-related_disorder": 1,
    "not_provided|Wiedemann-Steiner_syndrome|KMT2A-related_disorder": 2,
    "Wiedemann-Steiner_syndrome|not_provided": 43,
    "KMT2A-related_disorder|not_provided": 37,
    "not_specified|not_provided|Wiedemann-Steiner_syndrome": 1,
    "not_provided|KMT2A-related_disorder": 24,
    "Inborn_genetic_diseases|not_provided|KMT2A-related_disorder": 2,
    "Intellectual_disability|Wiedemann-Steiner_syndrome": 1,
    "Wiedemann-Steiner_syndrome|not_specified": 1,
    "KMT2A-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Wiedemann-Steiner_syndrome": 3,
    "not_provided|Wiedemann-Steiner_syndrome|Inborn_genetic_diseases": 2,
    "Wiedemann-Steiner_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "Wiedemann-Steiner_syndrome|See_cases|not_provided": 1,
    "Language_disorder|Atypical_behavior|Bilateral_ptosis|Neurodevelopmental_delay|not_provided": 1,
    "KMT2A-related_disorder|not_provided|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|KMT2A-related_disorder|not_specified|not_provided": 1,
    "Kabuki_syndrome_1|Wiedemann-Steiner_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Wiedemann-Steiner_syndrome|intellectual_deficiency": 1,
    "not_specified|not_provided|Wiedemann-Steiner_syndrome|Inborn_genetic_diseases": 1,
    "KMT2A-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Wiedemann-Steiner_syndrome|Inborn_genetic_diseases|Rare_genetic_intellectual_disability|not_provided|Hirsutism|Intellectual_disability": 1,
    "not_provided|KMT2A-related_disorder|Inborn_genetic_diseases": 2,
    "KMT2A-related_disorder|not_provided|Wiedemann-Steiner_syndrome": 3,
    "not_provided|KMT2A-related_disorder|Wiedemann-Steiner_syndrome": 2,
    "Wiedemann-Steiner_syndrome|not_provided|Neurodevelopmental_disorder": 1,
    "Wiedemann-Steiner_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Rubinstein_Taybi_like_syndrome": 3,
    "KMT2A-related_disorder|Intellectual_disability|not_provided": 1,
    "Kabuki_syndrome_1": 512,
    "Inborn_genetic_diseases|See_cases|Wiedemann-Steiner_syndrome": 1,
    "See_cases|not_provided|Wiedemann-Steiner_syndrome": 1,
    "KMT2A-related_disorder|not_specified|not_provided|Wiedemann-Steiner_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Wiedemann-Steiner_syndrome": 2,
    "Inborn_genetic_diseases|KMT2A-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|KMT2A-related_disorder": 1,
    "Intellectual_disability|not_provided|Inborn_genetic_diseases|Wiedemann-Steiner_syndrome": 1,
    "not_specified|Wiedemann-Steiner_syndrome": 1,
    "Inborn_genetic_diseases|KMT2A-related_disorder|not_provided": 2,
    "not_specified|not_provided|KMT2A-related_disorder": 2,
    "KMT2A-related_disorder|not_provided|Intellectual_disability|not_specified": 1,
    "not_provided|not_specified|Wiedemann-Steiner_syndrome": 1,
    "Wiedemann-Steiner_syndrome|Inborn_genetic_diseases": 1,
    "ARCN1-related_disorder|not_provided": 5,
    "not_provided|Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay": 2,
    "Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay": 21,
    "Inborn_genetic_diseases|Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay": 1,
    "ARCN1-related_disorder": 3,
    "Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay": 2,
    "not_provided|ARCN1-related_disorder": 3,
    "See_cases|ARCN1-related_disorder": 1,
    "Inborn_genetic_diseases|Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay|not_provided": 1,
    "Short_stature|_rhizomelic|_with_microcephaly|_micrognathia|_and_developmental_delay|not_provided|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta|_type_23": 2,
    "not_specified|TREH-related_disorder": 4,
    "TREH-related_disorder": 20,
    "not_specified|alpha|_alpha-Trehalase_deficiency": 1,
    "alpha|_alpha-Trehalase_deficiency": 1,
    "Intellectual_developmental_disorder_with_impaired_language_and_dysmorphic_facies": 18,
    "Intellectual_developmental_disorder_with_impaired_language_and_dysmorphic_facies|not_provided": 3,
    "DDX6-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_impaired_language_and_dysmorphic_facies": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_impaired_language_and_dysmorphic_facies": 1,
    "not_provided|DDX6-related_disorder": 1,
    "Mosaic_variegated_aneuploidy_syndrome_4": 3,
    "Neurodevelopmental_disorder_with_epilepsy|_spasticity|_and_brain_atrophy": 9,
    "TRAPPC4-related_disorder": 1,
    "Neurodevelopmental_disorder_with_epilepsy|_spasticity|_and_brain_atrophy|not_provided|Neurodevelopmental_disorder_with_progressive_microcephaly|_spasticity|_and_brain_anomalies": 1,
    "Glycogen_storage_disease|_type_I|not_provided": 4,
    "Glycogen_storage_disease|_type_I": 32,
    "not_provided|Glycogen_storage_disease|_type_I": 1,
    "Glucose-6-phosphate_transport_defect": 788,
    "not_specified|Glucose-6-phosphate_transport_defect": 5,
    "Glycogen_storage_disease|_type_I|SLC37A4-related_disorder": 1,
    "Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect": 10,
    "Glycogen_storage_disease_type_1_due_to_SLC37A4_mutation|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Glucose-6-phosphate_transport_defect|not_specified|not_provided": 1,
    "Glucose-6-phosphate_transport_defect|Inborn_genetic_diseases": 9,
    "Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|not_provided|not_specified": 1,
    "Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Congenital_disorder_of_glycosylation": 1,
    "not_provided|Glucose-6-phosphate_transport_defect": 21,
    "Glucose-6-phosphate_transport_defect|not_provided|SLC37A4-related_disorder|Inborn_genetic_diseases": 1,
    "SLC37A4-related_disorder": 4,
    "Inborn_genetic_diseases|Glucose-6-phosphate_transport_defect": 14,
    "Glucose-6-phosphate_transport_defect|Glycogen_storage_disease|_type_I": 6,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|not_provided|not_specified": 1,
    "Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect": 6,
    "Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 10,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Inborn_genetic_diseases": 2,
    "Glucose-6-phosphate_transport_defect|SLC37A4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect": 1,
    "Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Inborn_genetic_diseases": 1,
    "not_provided|Glucose-6-phosphate_transport_defect|Inborn_genetic_diseases": 1,
    "Glucose-6-phosphate_transport_defect|Phosphate_transport_defect": 4,
    "Glucose-6-phosphate_transport_defect|not_specified": 4,
    "Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect": 2,
    "Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect": 3,
    "Glucose-6-phosphate_transport_defect|not_specified|SLC37A4-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect": 1,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Inborn_genetic_diseases|Glycogen_storage_disease|_type_I|not_provided|Glycogen_storage_disease": 1,
    "Inborn_genetic_diseases|not_provided|Glucose-6-phosphate_transport_defect": 3,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|not_provided": 1,
    "not_provided|Glucose-6-phosphate_transport_defect|Glycogen_storage_disease": 1,
    "Inborn_genetic_diseases|SLC37A4-related_disorder|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect": 1,
    "Glucose-6-phosphate_transport_defect|not_provided": 10,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|not_provided": 2,
    "SLC37A4-related_disorder|Inborn_genetic_diseases|not_provided|Glucose-6-phosphate_transport_defect": 1,
    "SLC37A4-related_disorder|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect": 1,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 5,
    "Inborn_genetic_diseases|Glucose-6-phosphate_transport_defect|SLC37A4-related_disorder|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "SLC37A4-related_disorder|not_provided|Glucose-6-phosphate_transport_defect": 3,
    "Glucose-6-phosphate_transport_defect|not_provided|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect": 1,
    "SLC37A4-related_disorder|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect": 1,
    "Glycogen_storage_disease_type_1_due_to_SLC37A4_mutation|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|not_provided": 1,
    "SLC37A4-related_disorder|Inborn_genetic_diseases": 1,
    "Glucose-6-phosphate_transport_defect|SLC37A4-related_disorder": 3,
    "not_provided|Glucose-6-phosphate_transport_defect|SLC37A4-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|SLC37A4-related_disorder|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect": 1,
    "Glucose-6-phosphate_transport_defect|not_provided|not_specified": 1,
    "not_provided|SLC37A4-related_disorder|Glucose-6-phosphate_transport_defect": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|not_provided": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "not_provided|Inborn_genetic_diseases|Glucose-6-phosphate_transport_defect": 2,
    "Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Inborn_genetic_diseases|SLC37A4-related_disorder": 1,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|not_specified|not_provided": 2,
    "not_specified|not_provided|Glucose-6-phosphate_transport_defect": 1,
    "Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw|not_provided|Glucose-6-phosphate_transport_defect": 1,
    "Glucose-6-phosphate_transport_defect|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_I|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Inborn_genetic_diseases": 1,
    "not_provided|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|SLC37A4-related_disorder|Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "not_provided|Glycogen_storage_disease|_type_I|Inborn_genetic_diseases|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|not_specified": 1,
    "SLC37A4-related_disorder|Glucose-6-phosphate_transport_defect": 2,
    "not_specified|Glycogen_storage_disease|_type_I|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|not_provided": 1,
    "Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect|not_provided": 3,
    "Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|not_provided": 1,
    "SLC37A4-related_disorder|Inborn_genetic_diseases|Glucose-6-phosphate_transport_defect|not_provided|Glycogen_storage_disease|_type_I": 1,
    "Glucose-6-phosphate_transport_defect|not_provided|Inborn_genetic_diseases": 1,
    "See_cases|Glucose-6-phosphate_transport_defect": 1,
    "Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect": 1,
    "not_provided|Glucose-6-phosphate_transport_defect|not_specified|Glycogen_storage_disease|_type_I": 1,
    "not_provided|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|not_specified|Glycogen_storage_disease|_type_I": 1,
    "Inborn_genetic_diseases|SLC37A4-related_disorder|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect": 1,
    "Glucose-6-phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Inborn_genetic_diseases": 1,
    "Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw|not_provided": 1,
    "not_provided|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "Glucose-6-phosphate_transport_defect|Splenomegaly|Decreased_total_neutrophil_count|Decreased_total_leukocyte_count|Hepatomegaly|Immunodeficiency|Recurrent_respiratory_infections|Glycogen_storage_disease|_type_I|not_provided": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect": 1,
    "Glycogen_storage_disease|Glucose-6-phosphate_transport_defect|not_provided": 1,
    "Phosphate_transport_defect|Glucose-6-phosphate_transport_defect": 1,
    "Glycogen_storage_disease|_type_I|Glucose-6-phosphate_transport_defect": 1,
    "Congenital_disorder_of_glycosylation|_type_IIw|Phosphate_transport_defect|Glucose-6-phosphate_transport_defect|Inborn_genetic_diseases": 1,
    "SLC37A4-related_disorder|Congenital_disorder_of_glycosylation|_type_IIw|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect": 1,
    "Inborn_genetic_diseases|Glucose-6-phosphate_transport_defect|Phosphate_transport_defect|Congenital_disorder_of_glycosylation|_type_IIw": 1,
    "Glycogen_storage_disease|_type_I|not_specified": 1,
    "Glycogen_storage_disease|_type_I|not_specified|not_provided": 1,
    "Glycogen_storage_disease|_type_I|not_specified|SLC37A4-related_disorder": 1,
    "not_provided|Granulocytopenia_with_immunoglobulin_abnormality": 4,
    "not_provided|HYOU1-related_disorder": 6,
    "HYOU1-related_disorder|not_provided": 12,
    "HYOU1-related_disorder|not_specified|not_provided": 2,
    "HYOU1-related_disorder": 5,
    "Granulocytopenia_with_immunoglobulin_abnormality|not_provided|HYOU1-related_disorder": 1,
    "Granulocytopenia_with_immunoglobulin_abnormality|not_provided": 4,
    "Granulocytopenia_with_immunoglobulin_abnormality": 5,
    "not_specified|not_provided|Granulocytopenia_with_immunoglobulin_abnormality": 1,
    "Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome|not_provided": 3,
    "VPS11-related_disorder|not_provided": 1,
    "Dystonia_32": 1,
    "Hypomyelinating_leukodystrophy_12": 8,
    "VPS11-related_disorder": 2,
    "Hypomyelinating_leukodystrophy_12|not_provided": 4,
    "not_provided|Hypomyelinating_leukodystrophy_12": 1,
    "not_provided|Hypomyelinating_leukodystrophy_12|Dystonia_32": 1,
    "Dystonia_32|Hypomyelinating_leukodystrophy_12|not_provided": 2,
    "Hypomyelinating_leukodystrophy_12|Dystonia_32|not_provided": 1,
    "Hypomyelinating_leukodystrophy_12|Dystonia_32": 1,
    "not_provided|VPS11-related_disorder": 1,
    "Hypomyelinating_leukodystrophy_12|Leukoencephalopathy|not_provided": 1,
    "Dystonia_32|not_provided|Hypomyelinating_leukodystrophy_12": 1,
    "HMBS-related_disorder|not_provided": 5,
    "Porphyria|_acute_intermittent|_nonerythroid_variant": 2,
    "not_specified|Acute_intermittent_porphyria|not_provided": 1,
    "not_provided|Porphyria|_acute_intermittent|_nonerythroid_variant": 2,
    "Acute_intermittent_porphyria": 50,
    "not_provided|not_specified|Acute_intermittent_porphyria": 2,
    "Porphyria|_acute_intermittent|_nonerythroid_variant|not_provided": 1,
    "HMBS-related_disorder": 2,
    "not_provided|Acute_intermittent_porphyria": 30,
    "not_provided|Acute_intermittent_porphyria|not_specified": 2,
    "HMBS-related_disorder|not_specified|not_provided": 1,
    "Encephalopathy|_porphyria-related": 1,
    "Leukoencephalopathy|_porphyria-related": 1,
    "Encephalopathy|_porphyria-related|Leukoencephalopathy|_porphyria-related|Acute_intermittent_porphyria|not_provided|HMBS-related_disorder": 1,
    "not_provided|HMBS-related_disorder": 1,
    "Acute_intermittent_porphyria|not_provided|HMBS-related_disorder": 1,
    "Acute_intermittent_porphyria|Fever|Vomiting|Emotional_lability|Visual_loss|Abdominal_pain": 1,
    "Acute_intermittent_porphyria|HMBS-related_disorder|not_provided": 2,
    "Encephalopathy|_porphyria-related|not_provided|Acute_intermittent_porphyria": 2,
    "Encephalopathy|_porphyria-related|Leukoencephalopathy|_porphyria-related|Acute_intermittent_porphyria|not_provided": 1,
    "not_provided|Encephalopathy|_porphyria-related|Leukoencephalopathy|_porphyria-related|Acute_intermittent_porphyria": 2,
    "Acute_intermittent_porphyria|Encephalopathy|_porphyria-related|not_provided": 1,
    "Abnormal_circulating_porphyrin_concentration": 1,
    "Acute_intermittent_porphyria|Encephalopathy|_porphyria-related|Leukoencephalopathy|_porphyria-related|not_provided": 1,
    "not_specified|Acute_intermittent_porphyria|not_provided|Congenital_disorder_of_glycosylation": 1,
    "Acute_intermittent_porphyria|not_provided|not_specified": 2,
    "Anxiety": 1,
    "not_provided|Acute_intermittent_porphyria|HMBS-related_disorder": 3,
    "Leukoencephalopathy|_porphyria-related|Acute_intermittent_porphyria|not_specified|not_provided": 1,
    "Elevated_urinary_delta-aminolevulinic_acid|Acute_episodes_of_neuropathic_symptoms|Anxiety|Abdominal_pain": 1,
    "DPAGT1-congenital_disorder_of_glycosylation": 23,
    "Congenital_disorder_of_glycosylation|DPAGT1-congenital_disorder_of_glycosylation|not_provided|Acute_intermittent_porphyria": 1,
    "Congenital_disorder_of_glycosylation|not_provided|Acute_intermittent_porphyria|DPAGT1-congenital_disorder_of_glycosylation": 2,
    "Congenital_disorder_of_glycosylation|Acute_intermittent_porphyria|DPAGT1-congenital_disorder_of_glycosylation": 1,
    "not_provided|DPAGT1-congenital_disorder_of_glycosylation": 3,
    "DPAGT1-congenital_disorder_of_glycosylation|Acute_intermittent_porphyria": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 106,
    "Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation": 85,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation": 4,
    "not_provided|Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation": 2,
    "not_provided|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation|not_specified|not_provided|Congenital_disorder_of_glycosylation|Acute_intermittent_porphyria": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|not_specified": 3,
    "not_provided|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 4,
    "Congenital_myasthenic_syndrome_13": 9,
    "Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 2,
    "DPAGT1-related_disorder|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|not_provided|Acute_intermittent_porphyria": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|not_specified|DPAGT1-related_disorder": 1,
    "Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|Abnormality_of_metabolism/homeostasis": 1,
    "not_provided|Inborn_genetic_diseases|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|not_provided|DPAGT1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|DPAGT1-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation|DPAGT1-related_disorder": 1,
    "not_specified|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 1,
    "Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation|not_provided": 4,
    "not_specified|Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|not_provided|Congenital_disorder_of_glycosylation": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|not_provided|Congenital_myasthenic_syndrome_13": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_provided|Congenital_myasthenic_syndrome_13": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|Congenital_disorder_of_glycosylation": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|not_provided|DPAGT1-related_disorder|Congenital_myasthenic_syndrome_13": 1,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|not_provided": 4,
    "DPAGT1-congenital_disorder_of_glycosylation|Congenital_myasthenic_syndrome_13|Inborn_genetic_diseases": 3,
    "not_specified|DPAGT1-congenital_disorder_of_glycosylation|not_provided|Congenital_myasthenic_syndrome_13": 1,
    "Congenital_myasthenic_syndrome_13|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation": 1,
    "not_provided|Congenital_myasthenic_syndrome_13|DPAGT1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Noonan-like_syndrome": 13,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan-like_syndrome": 4,
    "Noonan-like_syndrome|not_provided": 2,
    "not_provided|Noonan-like_syndrome": 5,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan-like_syndrome|not_provided": 1,
    "CBL-related_disorder|not_provided": 18,
    "Noonan-like_syndrome|CBL-related_disorder|Juvenile_myelomonocytic_leukemia": 1,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|not_specified|CBL-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_specified|RASopathy": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|CBL-related_disorder|RASopathy": 6,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan-like_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|RASopathy|not_provided|not_specified": 1,
    "CBL-related_disorder|not_provided|RASopathy|not_specified": 1,
    "not_specified|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|RASopathy": 1,
    "not_provided|RASopathy|Cardiovascular_phenotype|CBL-related_disorder": 1,
    "RASopathy|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 2,
    "RASopathy|CBL-related_disorder": 6,
    "Cardiovascular_phenotype|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy|not_provided": 2,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|CBL-related_disorder": 4,
    "CBL-related_disorder|RASopathy": 15,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "CBL-related_disorder|Cardiovascular_phenotype": 5,
    "not_provided|CBL-related_disorder": 15,
    "Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|RASopathy|Cardiovascular_phenotype|CBL-related_disorder": 1,
    "RASopathy|not_specified|CBL-related_disorder|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|RASopathy": 1,
    "not_specified|RASopathy|not_provided|Cardiovascular_phenotype": 4,
    "CBL-related_disorder|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|RASopathy|CBL-related_disorder": 8,
    "Cardiovascular_phenotype|RASopathy|not_specified|CBL-related_disorder": 1,
    "CBL-related_disorder|RASopathy|Juvenile_myelomonocytic_leukemia|not_specified": 1,
    "CBL-related_disorder|RASopathy|Cardiovascular_phenotype": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype|CBL-related_disorder": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|RASopathy|CBL-related_disorder": 1,
    "RASopathy|CBL-related_disorder|Juvenile_myelomonocytic_leukemia": 4,
    "not_provided|RASopathy|CBL-related_disorder": 2,
    "Cardiovascular_phenotype|CBL-related_disorder": 1,
    "not_provided|CBL-related_disorder|Cardiovascular_phenotype|RASopathy|not_specified|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|not_specified|CBL-related_disorder|RASopathy": 1,
    "not_specified|Juvenile_myelomonocytic_leukemia|RASopathy|CBL-related_disorder": 1,
    "Cardiovascular_phenotype|RASopathy|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "CBL-related_disorder|Cardiovascular_phenotype|RASopathy": 6,
    "CBL-related_disorder|not_provided|RASopathy": 5,
    "RASopathy|not_provided|CBL-related_disorder|Juvenile_myelomonocytic_leukemia": 1,
    "RASopathy|Juvenile_myelomonocytic_leukemia|CBL-related_disorder": 2,
    "RASopathy|CBL-related_disorder|not_specified": 2,
    "not_provided|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy|not_specified": 1,
    "CBL-related_disorder|RASopathy|Noonan_syndrome": 1,
    "Inborn_genetic_diseases|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|RASopathy|Noonan_syndrome|Noonan_syndrome-like_disorder_with_juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome|CBL-related_disorder|Fragile_site_11b|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "Inborn_genetic_diseases|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Inborn_genetic_diseases|not_provided|CBL-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_provided": 2,
    "CBL-related_disorder|Neurodevelopmental_disorder|not_specified|RASopathy|Noonan_syndrome_1": 1,
    "CBL-related_disorder|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome-like_disorder_with_juvenile_myelomonocytic_leukemia|See_cases": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|RASopathy|not_provided": 2,
    "RASopathy|not_provided|Juvenile_myelomonocytic_leukemia|Noonan_syndrome-like_disorder_with_juvenile_myelomonocytic_leukemia": 1,
    "not_provided|CBL-related_disorder|RASopathy": 1,
    "not_provided|RASopathy|Noonan_syndrome-like_disorder_with_juvenile_myelomonocytic_leukemia": 2,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy|not_provided": 1,
    "RASopathy|not_provided|Hepatosplenomegaly|CBL-related_disorder": 1,
    "Epilepsy|_early-onset": 1,
    "CBL-related_disorder|RASopathy|not_specified|not_provided": 1,
    "CBL-related_disorder|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|RASopathy|not_provided": 1,
    "RASopathy|not_specified|Noonan-like_syndrome": 1,
    "CBL-related_disorder|Malignant_germ_cell_tumor_of_ovary|Cardiovascular_phenotype|Noonan_syndrome|not_provided|RASopathy|Noonan_syndrome-like_disorder_with_juvenile_myelomonocytic_leukemia|Juvenile_myelomonocytic_leukemia": 1,
    "CBL-related_disorder|not_provided|Intellectual_disability": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|See_cases|RASopathy": 1,
    "Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|Rhabdomyosarcoma|not_provided|RASopathy|Myeloproliferative_disorder": 1,
    "RASopathy|Cardiovascular_phenotype|CBL-related_disorder|Juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 2,
    "not_provided|RASopathy|CBL-related_disorder|Cardiovascular_phenotype": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|not_specified|RASopathy|not_provided": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|CBL-related_disorder|RASopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|not_specified|Juvenile_myelomonocytic_leukemia|CBL-related_disorder": 1,
    "CBL-related_disorder|RASopathy|not_provided|Cardiovascular_phenotype": 1,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy": 3,
    "RASopathy|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|Cardiovascular_phenotype": 1,
    "RASopathy|See_cases|not_provided": 1,
    "not_provided|RASopathy|CBL-related_disorder|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_specified": 1,
    "RASopathy|Noonan-like_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy|Cardiovascular_phenotype": 2,
    "RASopathy|CBL-related_disorder|Cardiovascular_phenotype": 6,
    "RASopathy|Cardiovascular_phenotype|See_cases": 1,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Cardiovascular_phenotype|RASopathy|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|RASopathy|Juvenile_myelomonocytic_leukemia|CBL-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|not_specified|not_provided|RASopathy": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|RASopathy|Juvenile_myelomonocytic_leukemia": 1,
    "CBL-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|RASopathy": 1,
    "not_specified|not_provided|RASopathy|CBL-related_disorder|Juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|not_provided|not_specified|RASopathy|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 1,
    "Cardiovascular_phenotype|Microcephaly": 1,
    "Cardiovascular_phenotype|not_specified|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|RASopathy|not_provided": 1,
    "not_specified|RASopathy|not_provided|CBL-related_disorder": 1,
    "RASopathy|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|not_specified": 1,
    "CBL-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|RASopathy|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|CBL-related_disorder|not_specified|RASopathy": 1,
    "B_lymphoblastic_leukemia_lymphoma_with_hyperdiploidy|not_specified|RASopathy": 1,
    "not_provided|RASopathy|not_specified|CBL-related_disorder": 1,
    "CBL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "not_specified|CBL-related_disorder|RASopathy": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|RASopathy": 1,
    "RASopathy|not_specified|Cardiovascular_phenotype|CBL-related_disorder": 1,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|not_specified|RASopathy": 1,
    "RASopathy|CBL-related_disorder|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia|not_specified|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|RASopathy|CBL-related_disorder|not_provided|not_specified": 1,
    "not_specified|RASopathy|CBL-related_disorder|Cardiovascular_phenotype": 2,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|not_specified|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|RASopathy|not_specified|CBL-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Juvenile_myelomonocytic_leukemia|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|RASopathy|CBL-related_disorder": 1,
    "RASopathy|CBL-related_disorder|not_specified|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "Cardiovascular_phenotype|CBL-related_disorder|RASopathy|not_specified": 1,
    "RASopathy|See_cases|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|RASopathy": 1,
    "CBL-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|CBL-related_disorder": 2,
    "CBL-related_disorder|not_specified|not_provided|RASopathy": 2,
    "not_provided|Cardiovascular_phenotype|CBL-related_disorder": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|not_specified|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Juvenile_myelomonocytic_leukemia": 2,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|CBL-related_disorder|not_specified": 1,
    "not_provided|not_specified|RASopathy|CBL-related_disorder": 2,
    "not_specified|CBL-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|not_provided|CBL-related_disorder|not_specified": 1,
    "RASopathy|not_provided|CBL-related_disorder|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|CBL-related_disorder": 1,
    "Cardiovascular_phenotype|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|not_specified|RASopathy": 1,
    "RASopathy|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|not_provided": 1,
    "CBL-related_disorder|not_specified|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "See_cases|RASopathy|not_specified|Juvenile_myelomonocytic_leukemia|CBL-related_disorder": 1,
    "RASopathy|not_specified|CBL-related_disorder": 1,
    "RASopathy|not_provided|Noonan-like_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|RASopathy|not_provided|not_specified|CBL-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|not_provided|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|CBL-related_disorder|RASopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|CBL-related_disorder|Juvenile_myelomonocytic_leukemia|RASopathy": 1,
    "RASopathy|CBL-related_disorder|Cardiovascular_phenotype|not_specified|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|CBL-related_disorder|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Juvenile_myelomonocytic_leukemia|CBL-related_disorder|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|CBL-related_disorder": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|not_specified": 1,
    "Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|CBL-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|CBL-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|RASopathy|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "CBL-related_disorder|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan-like_syndrome": 1,
    "Late-onset_retinal_degeneration|Isolated_microphthalmia_5": 13,
    "Late-onset_retinal_degeneration|Retinal_degeneration|Isolated_microphthalmia_5": 8,
    "Isolated_microphthalmia_5|Late-onset_retinal_degeneration": 11,
    "Isolated_microphthalmia_6|Retinal_degeneration|not_provided": 2,
    "Retinal_degeneration|Isolated_microphthalmia_5|Late-onset_retinal_degeneration": 1,
    "C1QTNF5-related_disorder|not_provided": 2,
    "not_provided|Late-onset_retinal_degeneration|Retinal_degeneration|Isolated_microphthalmia_5": 5,
    "C1QTNF5-related_disorder|not_provided|not_specified": 1,
    "Late-onset_retinal_degeneration|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Late-onset_retinal_degeneration": 1,
    "Late-onset_retinal_degeneration|Retinal_degeneration|Isolated_microphthalmia_5|not_provided": 1,
    "Isolated_microphthalmia_5|Late-onset_retinal_degeneration|not_provided|Retinal_dystrophy": 1,
    "C1QTNF5-related_disorder|not_provided|Isolated_microphthalmia_5|Late-onset_retinal_degeneration": 1,
    "not_provided|C1QTNF5-related_disorder": 1,
    "Late-onset_retinal_degeneration|Isolated_microphthalmia_5|not_specified|not_provided": 1,
    "Isolated_microphthalmia_5|not_provided|Retinal_dystrophy|Late-onset_retinal_degeneration": 1,
    "not_provided|Late-onset_retinal_degeneration|Isolated_microphthalmia_5": 1,
    "Late-onset_retinal_degeneration|Isolated_microphthalmia_5|Isolated_microphthalmia_6": 1,
    "Isolated_microphthalmia_5|Nanophthalmos_2": 3,
    "Isolated_microphthalmia_6|Retinal_degeneration": 2,
    "Retinal_degeneration": 2,
    "Isolated_microphthalmia_5|Late-onset_retinal_degeneration|Retinal_degeneration": 23,
    "Isolated_microphthalmia_5|Isolated_microphthalmia_6|Late-onset_retinal_degeneration": 5,
    "Isolated_microphthalmia_5|Late-onset_retinal_degeneration|not_provided|Retinal_degeneration": 1,
    "Isolated_microphthalmia_5": 443,
    "not_provided|Isolated_microphthalmia_5": 13,
    "Inborn_genetic_diseases|Isolated_microphthalmia_5": 15,
    "Retinal_degeneration|not_specified|not_provided|Isolated_microphthalmia_5": 2,
    "Isolated_microphthalmia_5|Nanophthalmos_2|not_provided|Nanophthalmia": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_5|not_provided": 1,
    "Isolated_microphthalmia_5|not_provided|Inborn_genetic_diseases": 1,
    "Isolated_microphthalmia_5|MFRP-related_disorder": 6,
    "MFRP-related_disorder": 3,
    "not_provided|Isolated_microphthalmia_5|Isolated_microphthalmia_6|not_specified|Retinal_degeneration": 1,
    "Isolated_microphthalmia_5|Retinal_degeneration|not_specified|not_provided": 1,
    "Isolated_microphthalmia_5|Nanophthalmos_2|not_provided": 1,
    "Isolated_microphthalmia_5|Retinal_dystrophy": 2,
    "MFRP-related_disorder|not_provided|Isolated_microphthalmia_5": 1,
    "Nanophthalmos_2": 3,
    "Retinal_dystrophy|Isolated_microphthalmia_5|Nanophthalmos_2": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_5|Retinal_dystrophy": 1,
    "Retinal_degeneration|not_provided|Isolated_microphthalmia_6|Isolated_microphthalmia_5": 1,
    "Retinal_dystrophy|Isolated_microphthalmia_5": 2,
    "Isolated_microphthalmia_5|Nanophthalmos_2|Retinal_dystrophy": 1,
    "Nanophthalmos_2|Isolated_microphthalmia_5": 2,
    "Isolated_microphthalmia_5|Inborn_genetic_diseases": 14,
    "Retinal_degeneration|MFRP-related_disorder|Retinal_dystrophy|not_provided|Isolated_microphthalmia_5|Late-onset_retinal_degeneration": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_5|not_provided|Late-onset_retinal_degeneration|Retinal_degeneration": 1,
    "Isolated_microphthalmia_5|not_provided|Retinal_dystrophy": 1,
    "not_provided|Isolated_microphthalmia_5|Isolated_microphthalmia_6|Retinal_degeneration": 1,
    "Inborn_genetic_diseases|not_provided|Isolated_microphthalmia_5": 4,
    "Inborn_genetic_diseases|Isolated_microphthalmia_5|Late-onset_retinal_degeneration|Retinal_degeneration": 4,
    "Inborn_genetic_diseases|Isolated_microphthalmia_5|Late-onset_retinal_degeneration|Retinal_degeneration|not_provided": 1,
    "Retinal_degeneration|MFRP-related_disorder|not_specified|not_provided|Isolated_microphthalmia_6|Isolated_microphthalmia_5": 1,
    "Retinal_degeneration|not_provided|not_specified|Isolated_microphthalmia_5|Late-onset_retinal_degeneration": 1,
    "Isolated_microphthalmia_5|not_provided": 3,
    "MFRP-related_disorder|not_specified|not_provided|Isolated_microphthalmia_5": 1,
    "Retinal_degeneration|not_specified|not_provided|Isolated_microphthalmia_6|Isolated_microphthalmia_5": 3,
    "not_provided|Isolated_microphthalmia_5|Nanophthalmos_2": 1,
    "Retinal_dystrophy|not_provided|Isolated_microphthalmia_5": 2,
    "MFRP-related_disorder|Retinal_dystrophy|Isolated_microphthalmia_5|Nanophthalmos_2|not_provided": 1,
    "Isolated_microphthalmia_5|MFRP-related_disorder|Late-onset_retinal_degeneration|Retinal_degeneration": 1,
    "Retinal_dystrophy|Isolated_microphthalmia_5|Nanophthalmos_2|not_provided": 1,
    "Retinal_degeneration|Isolated_microphthalmia_5|Nanophthalmos_2|not_specified|not_provided|Late-onset_retinal_degeneration": 1,
    "Isolated_microphthalmia_5|not_provided|Isolated_microphthalmia_6|Retinal_degeneration": 1,
    "not_provided|Late-onset_retinal_degeneration|Retinal_dystrophy|Retinal_degeneration|Isolated_microphthalmia_5": 1,
    "MFRP-related_disorder|Isolated_microphthalmia_6|Retinal_degeneration|Isolated_microphthalmia_5": 1,
    "Isolated_microphthalmia_5|Inborn_genetic_diseases|Late-onset_retinal_degeneration|Retinal_degeneration": 1,
    "Isolated_microphthalmia_5|Optic_atrophy": 1,
    "Retinal_degeneration|not_specified|Isolated_microphthalmia_5|Late-onset_retinal_degeneration": 1,
    "Retinal_degeneration|MFRP-related_disorder|not_provided|Isolated_microphthalmia_5": 1,
    "Retinal_degeneration|not_provided|Isolated_microphthalmia_5": 1,
    "not_provided|Retinal_degeneration": 1,
    "not_provided|Isolated_microphthalmia_6|Retinal_degeneration": 1,
    "Isolated_microphthalmia_6|not_provided|Retinal_degeneration": 1,
    "not_specified|Facial_hypotonia": 1,
    "NECTIN1-related_disorder": 9,
    "Cleft_lip/palate-ectodermal_dysplasia_syndrome|not_provided": 8,
    "Cleft_lip/palate-ectodermal_dysplasia_syndrome": 106,
    "not_provided|Cleft_lip/palate-ectodermal_dysplasia_syndrome": 28,
    "not_provided|Cleft_lip/palate-ectodermal_dysplasia_syndrome|NECTIN1-related_disorder": 2,
    "NECTIN1-related_disorder|not_provided|Cleft_lip/palate-ectodermal_dysplasia_syndrome": 1,
    "not_provided|Cleft_lip/palate-ectodermal_dysplasia_syndrome|not_specified": 1,
    "not_provided|NECTIN1-related_disorder": 1,
    "Inborn_genetic_diseases|Cleft_lip/palate-ectodermal_dysplasia_syndrome|not_provided": 1,
    "not_provided|NECTIN1-related_disorder|Cleft_lip/palate-ectodermal_dysplasia_syndrome": 1,
    "Cleft_lip/palate-ectodermal_dysplasia_syndrome|Orofacial_cleft_7": 1,
    "Cleft_lip/palate-ectodermal_dysplasia_syndrome|not_provided|NECTIN1-related_disorder": 1,
    "Cleft_lip/palate-ectodermal_dysplasia_syndrome|NECTIN1-related_disorder|not_provided": 2,
    "NECTIN1-related_disorder|not_provided": 1,
    "Glaucoma": 1,
    "TBCEL-related_disorder": 1,
    "not_provided|Nonsyndromic_Hearing_Loss|_Dominant|Hearing_loss|_autosomal_recessive|not_specified": 1,
    "TECTA-related_disorder": 21,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12": 27,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21": 27,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21": 18,
    "not_provided|TECTA-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 29,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 7,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 2,
    "Deafness|_neurosensory_autosomal_recessive_21": 2,
    "Hearing_impairment|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Nonsyndromic_genetic_hearing_loss|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|TECTA-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21": 1,
    "Inborn_genetic_diseases|TECTA-related_disorder": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Hearing_loss|_autosomal_recessive": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified": 1,
    "TECTA-related_disorder|not_provided": 5,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_specified|not_provided": 3,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 4,
    "not_provided|TECTA-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Nonsyndromic_Hearing_Loss|_Dominant|Hearing_loss|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 6,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|Inborn_genetic_diseases": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|Ear_malformation": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|TECTA-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|TECTA-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 7,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_12": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|Hearing_impairment": 1,
    "Hearing_impairment|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|TECTA-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_21|Nonsyndromic_genetic_hearing_loss": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 1,
    "Rare_genetic_deafness|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified|not_provided": 3,
    "not_provided|TECTA-related_disorder": 7,
    "Inborn_genetic_diseases|not_provided|TECTA-related_disorder": 1,
    "TECTA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided": 3,
    "not_specified|TECTA-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|Deafness|_neurosensory_autosomal_recessive_21|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|TECTA-related_disorder": 1,
    "TECTA-related_disorder|Nonsyndromic_genetic_hearing_loss|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21": 3,
    "not_provided|not_specified|TECTA-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_specified": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_specified|TECTA-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|TECTA-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "TECTA-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Hearing_impairment": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|Meniere_disease|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 2,
    "TECTA-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_21|Meniere_disease": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "not_specified|Congenital_sensorineural_hearing_impairment|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|TECTA-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "TECTA-related_disorder|not_specified|not_provided": 1,
    "Bilateral_sensorineural_hearing_impairment|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_21|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Rare_genetic_deafness|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|See_cases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_21|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_12|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided": 1,
    "not_specified|TECTA-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_21|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_12|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|not_provided|TECTA-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_21|TECTA-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_12": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_12|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_12|TECTA-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_21": 1,
    "TECTA-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Lathosterolosis": 130,
    "Lathosterolosis|not_provided": 3,
    "not_provided|Lathosterolosis": 6,
    "Inborn_genetic_diseases|not_provided|Lathosterolosis": 1,
    "SC5D-related_disorder": 1,
    "not_provided|not_specified|Lathosterolosis": 1,
    "SC5D-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Lathosterolosis": 1,
    "SORL1-related_disorder|not_provided": 12,
    "SORL1-related_disorder": 4,
    "SORL1-related_disorder|not_provided|not_specified": 2,
    "not_provided|SORL1-related_disorder": 9,
    "Complex_hereditary_spastic_paraplegia": 1,
    "not_provided|Early-onset_dementia_of_unclear_type": 1,
    "Alzheimer_disease_9": 18,
    "SORL1-related_disorder|not_specified|not_provided": 2,
    "not_provided|SORL1-related_disorder|not_specified": 1,
    "Lennox-Gastaut_syndrome": 3,
    "CLMP-related_disorder": 2,
    "Congenital_short_bowel_syndrome|_autosomal_recessive": 6,
    "Congenital_short_bowel_syndrome|_autosomal_recessive|Intestinal_pseudo-obstruction": 1,
    "Congenital_short_bowel_syndrome|_autosomal_recessive|Congenital_short_bowel_syndrome|Intestinal_pseudo-obstruction|not_provided": 1,
    "CLMP-related_disorder|not_provided": 2,
    "GRAMD1B-related_disorder": 12,
    "not_specified|GRAMD1B-related_disorder": 1,
    "not_provided|GRAMD1B-related_disorder": 1,
    "Brugada_syndrome_7": 47,
    "Cardiovascular_phenotype|Brugada_syndrome_7": 20,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_7": 1,
    "Brugada_syndrome_7|not_provided|Cardiovascular_phenotype": 3,
    "Brugada_syndrome_7|Cardiovascular_phenotype": 18,
    "not_provided|Brugada_syndrome_7": 1,
    "Brugada_syndrome_7|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Brugada_syndrome_7": 1,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome_7|not_provided": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_7|SCN3B-related_disorder": 1,
    "Atrial_fibrillation|_familial|_16": 2,
    "Cardiac_arrhythmia|Brugada_syndrome_7": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_7|not_specified": 1,
    "Brugada_syndrome_7|Inborn_genetic_diseases": 1,
    "not_provided|Brugada_syndrome_7|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_7|Cardiac_arrhythmia": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Brugada_syndrome_7": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_7": 1,
    "not_provided|Atrial_fibrillation|_familial|_16|Brugada_syndrome_7": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_7": 2,
    "Cardiomyopathy|not_provided|SCN3B-related_disorder|not_specified|Brugada_syndrome_7|Death_in_infancy|Cardiovascular_phenotype": 1,
    "SCN3B-related_disorder|Brugada_syndrome_7|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_7": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Brugada_syndrome_7": 1,
    "not_provided|Brugada_syndrome_7|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_7|not_provided": 1,
    "Brugada_syndrome_7|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Brugada_syndrome_7": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_16|not_specified|Brugada_syndrome|not_provided|Brugada_syndrome_7": 1,
    "Brugada_syndrome_7|Brugada_syndrome": 1,
    "not_provided|SIAE-related_disorder": 7,
    "SIAE-related_disorder|not_provided": 2,
    "Autoimmune_disease|_susceptibility_to|_6": 2,
    "not_provided|Juvenile_idiopathic_arthritis": 1,
    "Autoimmune_disease|_susceptibility_to|_6|not_specified|not_provided": 1,
    "Autoimmune_disease|_susceptibility_to|_6|not_provided": 1,
    "SIAE-related_disorder": 1,
    "SIAE-related_disorder|not_specified|not_provided|Autoimmune_disease|_susceptibility_to|_6": 1,
    "not_provided|Autoimmune_disease|_susceptibility_to|_6": 1,
    "not_provided|not_specified|SIAE-related_disorder": 1,
    "Neurodevelopmental_disorder_with_intracranial_hemorrhage|_seizures|_and_spasticity": 3,
    "See_cases|Neurodevelopmental_disorder_with_intracranial_hemorrhage|_seizures|_and_spasticity": 4,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 87,
    "Inborn_genetic_diseases|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 5,
    "not_provided|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 31,
    "ROBO3-related_disorder": 13,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|not_provided": 6,
    "ROBO3-related_disorder|not_provided": 3,
    "not_provided|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Tuberous_sclerosis_syndrome": 2,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|ROBO3-related_disorder|Inborn_genetic_diseases": 1,
    "ROBO3-related_disorder|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|not_provided": 1,
    "not_provided|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|ROBO3-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|ROBO3-related_disorder": 1,
    "ROBO3-related_disorder|not_provided|Inborn_genetic_diseases|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 1,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|Inborn_genetic_diseases": 5,
    "ROBO3-related_disorder|Inborn_genetic_diseases": 2,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|ROBO3-related_disorder": 1,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|ROBO3-related_disorder|not_provided": 1,
    "not_provided|ROBO3-related_disorder": 4,
    "Conjugate_gaze_palsy|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 1,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1|not_provided|Inborn_genetic_diseases": 1,
    "ROBO3-related_disorder|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 1,
    "not_provided|Inborn_genetic_diseases|ROBO3-related_disorder|not_specified|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis_1": 1,
    "ROBO4-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "ROBO4-related_disorder|not_provided": 1,
    "Aortic_valve_disease_3": 16,
    "Thoracic_aortic_aneurysm": 3,
    "ROBO4-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Bicuspid_aortic_valve|Ascending_tubular_aorta_aneurysm": 4,
    "not_specified|Aortic_valve_disease_3": 3,
    "ROBO4-related_disorder": 7,
    "Bicuspid_aortic_valve|Ascending_tubular_aorta_aneurysm|Aortic_valve_disease_3": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ROBO4-related_disorder": 4,
    "not_provided|ROBO4-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ROBO4-related_disorder|not_specified|not_provided|Aortic_valve_disease_3": 1,
    "Aortic_valve_disease_3|not_provided": 1,
    "Ascending_tubular_aorta_aneurysm|Bicuspid_aortic_valve": 3,
    "Aortic_valve_disease_3|Ascending_tubular_aorta_aneurysm|Bicuspid_aortic_valve|ROBO4-related_disorder": 1,
    "ROBO4-related_disorder|not_specified|Aortic_valve_disease_3": 1,
    "Aortic_valve_disease_3|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|ROBO4-related_disorder": 2,
    "not_specified|ROBO4-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ROBO4-related_disorder|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ROBO4-related_disorder": 3,
    "Ascending_tubular_aorta_aneurysm|Bicuspid_aortic_valve|Aortic_valve_disease_3": 1,
    "ROBO4-related_disorder|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ROBO4-related_disorder|not_specified|not_provided": 1,
    "ROBO4-related_disorder|Ascending_tubular_aorta_aneurysm|Bicuspid_aortic_valve": 1,
    "Aortic_valve_disease_3|Bicuspid_aortic_valve|Ascending_tubular_aorta_aneurysm": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 83,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided": 23,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 18,
    "not_specified|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 2,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A": 6,
    "Intellectual_disability|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|not_specified": 1,
    "Inborn_genetic_diseases|HEPACAM-related_disorder|not_provided": 1,
    "HEPACAM-related_disorder|Inborn_genetic_diseases|Intellectual_disability|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided": 1,
    "not_provided|HEPACAM-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "HEPACAM-related_disorder": 2,
    "HEPACAM-related_disorder|not_provided": 5,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_specified|not_provided": 3,
    "not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_provided": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|not_provided": 3,
    "Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided": 2,
    "not_provided|HEPACAM-related_disorder": 4,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|Autism_spectrum_disorder": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided|Inborn_genetic_diseases": 3,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|not_provided": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability": 1,
    "Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided": 1,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_specified": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_provided": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_provided": 3,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|HEPACAM-related_disorder|not_provided": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|not_specified|not_provided": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 154,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A": 1,
    "HEPACAM-related_disorder|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|not_provided": 1,
    "MEGALENCEPHALIC_LEUKOENCEPHALOPATHY_WITH_SUBCORTICAL_CYSTS_2B|_REMITTING|_WITH_IMPAIRED_INTELLECTUAL_DEVELOPMENT|not_provided": 1,
    "HEPACAM-related_disorder|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 2,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2A|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_2B|_remitting|_with_or_without_intellectual_disability|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Joubert_syndrome_39|not_specified": 1,
    "Joubert_syndrome|Joubert_syndrome_39|Meckel_syndrome|_type_4": 1,
    "Meckel_syndrome|_type_4": 7,
    "Joubert_syndrome_39": 1,
    "Joubert_syndrome|Joubert_syndrome_39": 1,
    "not_provided|Congenital_disorder_of_glycosylation|_type_Iw|_autosomal_dominant": 2,
    "not_specified|STT3A-related_disorder": 1,
    "STT3A-congenital_disorder_of_glycosylation": 4,
    "not_provided|STT3A-related_disorder": 2,
    "STT3A-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|_type_Iw|_autosomal_dominant": 2,
    "not_provided|STT3A-congenital_disorder_of_glycosylation": 4,
    "not_specified|STT3A-congenital_disorder_of_glycosylation|not_provided": 2,
    "Congenital_disorder_of_glycosylation|_type_Iw|_autosomal_dominant|STT3A-congenital_disorder_of_glycosylation": 1,
    "not_provided|STT3A-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|_type_Iw|_autosomal_dominant": 1,
    "CHEK1-related_disorder": 24,
    "CHEK1-related_disorder|not_provided": 5,
    "not_specified|CHEK1-related_disorder": 1,
    "Oocyte/zygote/embryo_maturation_arrest_21": 5,
    "CHEK1-related_disorder|not_specified": 1,
    "not_provided|Male_infertility_due_to_gonadal_dysgenesis_or_sperm_disorder": 1,
    "Hydrolethalus_syndrome": 32,
    "not_provided|Hydrolethalus_syndrome": 14,
    "not_provided|Severe_growth_deficiency-strabismus-extensive_dermal_melanocytosis-intellectual_disability_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Severe_growth_deficiency-strabismus-extensive_dermal_melanocytosis-intellectual_disability_syndrome": 1,
    "Severe_growth_deficiency-strabismus-extensive_dermal_melanocytosis-intellectual_disability_syndrome": 9,
    "not_provided|PUS3-related_disorder": 4,
    "Inborn_genetic_diseases|PUS3-related_disorder": 1,
    "PUS3-related_disorder|Heart|_malformation_of|Aplasia/Hypoplasia_of_the_cerebellum|Anencephaly|Polyhydramnios|Ankle_flexion_contracture|not_provided": 1,
    "PUS3-related_disorder": 1,
    "PUS3-related_disorder|not_provided": 1,
    "Severe_growth_deficiency-strabismus-extensive_dermal_melanocytosis-intellectual_disability_syndrome|Genetic_syndrome_with_a_Dandy-Walker_malformation_as_major_feature|not_provided|Dandy-Walker_syndrome": 1,
    "Dandy-Walker_syndrome|not_provided|Genetic_syndrome_with_a_Dandy-Walker_malformation_as_major_feature|Severe_growth_deficiency-strabismus-extensive_dermal_melanocytosis-intellectual_disability_syndrome": 1,
    "Severe_growth_deficiency-strabismus-extensive_dermal_melanocytosis-intellectual_disability_syndrome|not_provided": 3,
    "Heart|_malformation_of|Aplasia/Hypoplasia_of_the_cerebellum|Anencephaly|Polyhydramnios|Ankle_flexion_contracture": 1,
    "HYLS1-related_disorder": 1,
    "Hydrolethalus_syndrome|not_provided": 2,
    "Hydrolethalus_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Hydrolethalus_syndrome_1": 15,
    "not_provided|Hydrolethalus_syndrome_1|HYLS1-related_disorder|Hydrolethalus_syndrome": 1,
    "Hydrolethalus_syndrome_1|Hydrolethalus_syndrome": 3,
    "Hydrolethalus_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Hydrolethalus_syndrome_1|Hydrolethalus_syndrome": 2,
    "Hydrolethalus_syndrome|Inborn_genetic_diseases": 2,
    "Hydrolethalus_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hydrolethalus_syndrome": 1,
    "Hydrolethalus_syndrome|Hydrolethalus_syndrome_1": 1,
    "Holoprosencephaly_11": 300,
    "not_provided|Holoprosencephaly_11": 31,
    "Holoprosencephaly_11|not_provided": 13,
    "Holoprosencephaly_11|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|Holoprosencephaly_11": 14,
    "Inborn_genetic_diseases|CDON-related_disorder|Holoprosencephaly_11": 2,
    "not_provided|Holoprosencephaly_11|Holoprosencephaly_1|not_specified": 1,
    "Holoprosencephaly_11|CDON-related_disorder": 7,
    "Holoprosencephaly_11|Inborn_genetic_diseases|not_provided": 2,
    "CDON-related_disorder|Holoprosencephaly_11": 9,
    "Holoprosencephaly_11|Inborn_genetic_diseases|CDON-related_disorder": 1,
    "not_provided|not_specified|Holoprosencephaly_11": 14,
    "CDON-related_disorder": 15,
    "Abnormal_brain_morphology|not_specified|not_provided": 1,
    "not_provided|CDON-related_disorder": 2,
    "not_specified|Holoprosencephaly_11": 4,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_11": 2,
    "Inborn_genetic_diseases|Holoprosencephaly_11|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Holoprosencephaly_11": 1,
    "not_specified|Inborn_genetic_diseases|Holoprosencephaly_11|not_provided": 1,
    "CDON-related_disorder|not_provided|Holoprosencephaly_11": 3,
    "Inborn_genetic_diseases|Holoprosencephaly_11|CDON-related_disorder|not_provided": 1,
    "Holoprosencephaly_11|CDON-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Holoprosencephaly_11": 1,
    "Holoprosencephaly_11|Intellectual_disability": 1,
    "not_provided|Holoprosencephaly_11|Holoprosencephaly_sequence": 1,
    "Holoprosencephaly_spectrum_disorder|Holoprosencephaly_11": 1,
    "Holoprosencephaly_11|not_provided|CDON-related_disorder": 1,
    "Microcephaly|Holoprosencephaly_11": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_11|not_provided": 1,
    "not_specified|not_provided|Holoprosencephaly_11": 2,
    "not_specified|Holoprosencephaly_11|not_provided": 1,
    "Holoprosencephaly_11|not_specified|Inborn_genetic_diseases": 1,
    "Holoprosencephaly_11|not_specified|not_provided": 1,
    "SRPRA-related_disorder": 6,
    "SRPRA-related_disorder|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_19|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_19": 5,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 4,
    "FOXRED1-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_19": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_19|not_provided": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_19": 11,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_provided": 3,
    "Mitochondrial_encephalopathy": 1,
    "not_provided|FOXRED1-related_disorder": 2,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_19|Mitochondrial_complex_I_deficiency": 1,
    "not_specified|FOXRED1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_19|Mitochondrial_complex_I_deficiency|Inborn_genetic_diseases|not_provided|Mitochondrial_disease|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_19|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_19|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_19|FOXRED1-related_disorder|not_provided|Leigh_syndrome": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_19|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_19|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_19": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_19|Inborn_genetic_diseases|not_provided": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_19|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_19|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Seizure": 1,
    "Inborn_genetic_diseases|Developmental_delay|Leigh_syndrome|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_19": 1,
    "TIRAP-related_disorder": 4,
    "not_specified|TIRAP-related_disorder": 1,
    "Malaria|_susceptibility_to|Mycobacterium_tuberculosis|_susceptibility_to|Bacteremia|_susceptibility_to|_1|not_provided|Invasive_pneumococcal_disease|_protection_against|Malaria|_resistance_to|Mycobacterium_tuberculosis|_protection_against|Bacteremia|_susceptibility|not_specified": 1,
    "not_specified|Al-Raqad_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Al-Raqad_syndrome|not_provided": 1,
    "Al-Raqad_syndrome": 14,
    "not_provided|Al-Raqad_syndrome": 1,
    "Inborn_genetic_diseases|Al-Raqad_syndrome": 2,
    "DCPS-related_disorder|not_provided": 4,
    "DCPS-related_disorder": 1,
    "Al-Raqad_syndrome|not_provided|DCPS-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|DCPS-related_disorder": 1,
    "KIRREL3-related_disorder": 12,
    "not_provided|Intellectual_disability|_autosomal_dominant_4": 1,
    "KIRREL3-related_disorder|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_4": 4,
    "not_specified|KIRREL3-related_disorder": 1,
    "Difficulty_walking|Thoracic_scoliosis|Absent_speech|Global_developmental_delay": 1,
    "KIRREL3-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_4": 1,
    "KIRREL3-related_disorder|not_specified|not_provided": 1,
    "KIRREL3-related_disorder|not_specified": 2,
    "11q_partial_monosomy_syndrome": 1,
    "not_specified|ETS1-related_disorder": 1,
    "ETS1-related_disorder": 1,
    "FLI1-related_disorder": 7,
    "Bleeding_disorder|_platelet-type|_21": 7,
    "not_specified|not_provided|FLI1-related_disorder|Bleeding_disorder|_platelet-type|_21": 1,
    "FLI1-related_disorder|not_provided": 5,
    "not_provided|FLI1-related_disorder": 7,
    "not_provided|Bleeding_disorder|_platelet-type|_21": 2,
    "Bleeding_disorder|_platelet-type|_21|Inborn_genetic_diseases": 1,
    "Bleeding_disorder_platelet_type_macrothrombocytopenia|Bleeding_disorder|_platelet-type|_21": 1,
    "Thrombocytopenia|Abnormal_bleeding|Bleeding_disorder|_platelet-type|_21": 1,
    "not_provided|11q_partial_monosomy_syndrome|Bleeding_disorder|_platelet-type|_21": 1,
    "Antenatal_Bartter_syndrome|not_provided": 5,
    "Bartter_disease_type_2": 89,
    "not_provided|Bartter_disease_type_2": 18,
    "Antenatal_Bartter_syndrome": 3,
    "Bartter_disease_type_2|not_provided": 18,
    "Inborn_genetic_diseases|KCNJ1-related_disorder|Bartter_disease_type_2|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Bartter_disease_type_2": 1,
    "not_provided|not_specified|Bartter_disease_type_2|KCNJ1-related_disorder": 1,
    "Bartter_disease_type_2|Inborn_genetic_diseases": 5,
    "KCNJ1-related_disorder": 1,
    "not_provided|Bartter_disease_type_2|Bartter_syndrome": 1,
    "Inborn_genetic_diseases|Bartter_disease_type_2": 1,
    "not_specified|not_provided|Bartter_disease_type_2": 1,
    "Bartter_syndrome|not_provided|Bartter_disease_type_2": 1,
    "Bartter_disease_type_2|not_provided|Bartter_syndrome": 2,
    "not_provided|KCNJ1-related_disorder|Bartter_disease_type_2": 1,
    "Bartter_disease_type_2|Bartter_syndrome|not_provided": 3,
    "not_provided|KCNJ1-related_disorder": 2,
    "KCNJ1-related_disorder|not_provided": 1,
    "Bartter_disease_type_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Bartter_disease_type_2|not_specified|not_provided": 1,
    "Bartter_syndrome|Bartter_disease_type_2": 1,
    "not_provided|Bartter_disease_type_2|KCNJ1-related_disorder": 1,
    "not_provided|Bartter_disease_type_2|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Bartter_disease_type_2": 1,
    "not_provided|Antenatal_Bartter_syndrome|KCNJ1-related_disorder": 1,
    "not_specified|Bartter_disease_type_2": 1,
    "not_specified|not_provided|Antenatal_Bartter_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_2": 1,
    "Bartter_disease_type_2|not_specified|not_provided": 1,
    "Familial_hyperaldosteronism|Congenital_long_QT_syndrome": 16,
    "Familial_hyperaldosteronism_type_III": 17,
    "Familial_hyperaldosteronism_type_III|not_provided": 5,
    "Congenital_long_QT_syndrome|Familial_hyperaldosteronism": 18,
    "Congenital_long_QT_syndrome|not_provided|Familial_hyperaldosteronism": 2,
    "Familial_hyperaldosteronism|Congenital_long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Familial_hyperaldosteronism_type_III": 4,
    "not_provided|Familial_hyperaldosteronism|Congenital_long_QT_syndrome": 4,
    "Familial_hyperaldosteronism_type_III|not_provided|Congenital_long_QT_syndrome": 7,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Familial_hyperaldosteronism|Congenital_long_QT_syndrome": 2,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|not_provided|Familial_hyperaldosteronism|Congenital_long_QT_syndrome": 1,
    "Familial_hyperaldosteronism_type_III|not_provided|Long_QT_syndrome_13": 1,
    "Familial_hyperaldosteronism_type_III|Congenital_long_QT_syndrome": 10,
    "Congenital_long_QT_syndrome|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 1,
    "Congenital_long_QT_syndrome|Familial_hyperaldosteronism_type_III": 9,
    "Cardiovascular_phenotype|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 2,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 15,
    "Cardiovascular_phenotype|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 2,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Long_QT_syndrome|Cardiovascular_phenotype": 3,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|not_specified|Long_QT_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome|Primary_dilated_cardiomyopathy|Congenital_long_QT_syndrome|Familial_hyperaldosteronism_type_III|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome_13|Cardiovascular_phenotype|not_specified|Familial_hyperaldosteronism_type_III|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "KCNJ5-related_disorder": 2,
    "not_provided|Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|not_provided": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Long_QT_syndrome": 2,
    "Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|KCNJ5-related_disorder|Long_QT_syndrome|Familial_hyperaldosteronism|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 1,
    "not_provided|Cardiovascular_phenotype|KCNJ5-related_disorder|Long_QT_syndrome": 1,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Long_QT_syndrome": 3,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 2,
    "Cardiovascular_phenotype|not_provided|Familial_hyperaldosteronism_type_III|Congenital_long_QT_syndrome|Long_QT_syndrome|Long_QT_syndrome_13": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|not_specified|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Aldosterone-producing_adrenal_adenoma|_somatic|not_provided|Long_QT_syndrome|Familial_hyperaldosteronism_type_III": 1,
    "Long_QT_syndrome|Familial_hyperaldosteronism_type_III": 2,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome": 1,
    "Aldosterone-producing_adrenal_adenoma|_somatic|Familial_hyperaldosteronism_type_III|Andersen_Tawil_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 2,
    "Long_QT_syndrome|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 5,
    "not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 4,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome|Familial_hyperaldosteronism_type_III": 2,
    "KCNJ5-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "KCNJ5-related_disorder|Hypertrophic_cardiomyopathy|Long_QT_syndrome": 1,
    "not_specified|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Long_QT_syndrome": 1,
    "KCNJ5-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|KCNJ5-related_disorder|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Long_QT_syndrome": 1,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|not_provided|Long_QT_syndrome": 1,
    "not_provided|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 1,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Congenital_long_QT_syndrome|not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 1,
    "Long_QT_syndrome|KCNJ5-related_disorder|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|KCNJ5-related_disorder|Cardiovascular_phenotype|not_provided|Familial_hyperaldosteronism_type_III": 1,
    "Long_QT_syndrome|not_specified|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Cardiovascular_phenotype": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome|Familial_hyperaldosteronism_type_III": 1,
    "Long_QT_syndrome_13|Cardiovascular_phenotype|Familial_hyperaldosteronism_type_III|not_provided|not_specified|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|KCNJ5-related_disorder": 1,
    "Long_QT_syndrome|Long_QT_syndrome_13|not_provided|Familial_hyperaldosteronism_type_III|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified": 1,
    "not_provided|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 1,
    "Long_QT_syndrome|not_provided|KCNJ5-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Long_QT_syndrome_13|KCNJ5-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Familial_hyperaldosteronism_type_III|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome_13|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 1,
    "not_specified|Familial_hyperaldosteronism_type_III|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome_13|not_provided|not_specified|Familial_hyperaldosteronism_type_III|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|not_provided": 1,
    "Familial_hyperaldosteronism_type_III|not_specified|Congenital_long_QT_syndrome|KCNJ5-related_disorder|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 1,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|KCNJ5-related_disorder|not_provided|Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III": 1,
    "Long_QT_syndrome|See_cases": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|KCNJ5-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Familial_hyperaldosteronism_type_III|Andersen_Tawil_syndrome|Long_QT_syndrome_13": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13": 1,
    "Long_QT_syndrome|Long_QT_syndrome_13|Familial_hyperaldosteronism_type_III|Cardiovascular_phenotype": 1,
    "Familial_hyperaldosteronism_type_III|Congenital_long_QT_syndrome|not_provided": 5,
    "Familial_hyperaldosteronism_type_III|Long_QT_syndrome_13|Congenital_long_QT_syndrome": 1,
    "not_provided|ARHGAP32-related_disorder": 10,
    "ARHGAP32-related_disorder|not_provided": 4,
    "ARHGAP32-related_disorder": 23,
    "ARHGAP32-related_disorder|not_specified": 1,
    "not_specified|not_provided|ARHGAP32-related_disorder": 1,
    "Birt-Hogg-Dube_syndrome_2|not_specified": 1,
    "Autosomal_recessive_congenital_ichthyosis_11": 7,
    "not_provided|ST14-related_disorder": 7,
    "ST14-related_disorder|not_provided": 5,
    "ST14-related_disorder": 5,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_11": 4,
    "Autosomal_recessive_congenital_ichthyosis_11|not_provided": 2,
    "Autosomal_recessive_congenital_ichthyosis_11|Ichthyosis": 1,
    "Arthrogryposis|_distal|_type_12": 5,
    "OPCML-related_disorder": 4,
    "IGSF9B-related_condition": 1,
    "Porencephaly-microcephaly-bilateral_congenital_cataract_syndrome": 13,
    "not_provided|JAM3-related_disorder": 3,
    "JAM3-related_disorder|not_provided": 4,
    "not_provided|Porencephaly-microcephaly-bilateral_congenital_cataract_syndrome": 3,
    "Porencephaly-microcephaly-bilateral_congenital_cataract_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|JAM3-related_disorder": 1,
    "JAM3-related_disorder": 2,
    "JAM3-related_disorder|Porencephaly-microcephaly-bilateral_congenital_cataract_syndrome|not_provided": 1,
    "NCAPD3-related_disorder": 38,
    "Microcephaly_22|_primary|_autosomal_recessive": 12,
    "NCAPD3-related_disorder|not_provided": 5,
    "not_provided|NCAPD3-related_disorder": 4,
    "not_provided|NCAPD3-related_disorder|Microcephaly_22|_primary|_autosomal_recessive": 1,
    "NCAPD3-related_disorder|Microcephaly_22|_primary|_autosomal_recessive": 1,
    "not_specified|Microcephaly_22|_primary|_autosomal_recessive": 1,
    "Microcephaly_22|_primary|_autosomal_recessive|not_specified": 2,
    "Intellectual_disability|NCAPD3-related_disorder|not_provided": 2,
    "not_provided|Microcephaly_22|_primary|_autosomal_recessive": 1,
    "not_specified|NCAPD3-related_disorder": 1,
    "Microcephaly_22|_primary|_autosomal_recessive|not_provided": 3,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase|not_provided": 14,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase": 150,
    "not_provided|Deficiency_of_isobutyryl-CoA_dehydrogenase": 17,
    "not_specified|not_provided|Deficiency_of_isobutyryl-CoA_dehydrogenase": 3,
    "Inborn_genetic_diseases|Deficiency_of_isobutyryl-CoA_dehydrogenase": 4,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase|Inborn_genetic_diseases|not_provided": 1,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase|Inborn_genetic_diseases": 6,
    "not_specified|Deficiency_of_isobutyryl-CoA_dehydrogenase|not_provided": 1,
    "ACAD8-related_disorder|not_provided|Deficiency_of_isobutyryl-CoA_dehydrogenase": 1,
    "not_provided|Deficiency_of_isobutyryl-CoA_dehydrogenase|ACAD8-related_disorder": 1,
    "ACAD8-related_disorder|Deficiency_of_isobutyryl-CoA_dehydrogenase": 2,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_isobutyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase|not_specified|not_provided": 1,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase|ACAD8-related_disorder": 1,
    "Deficiency_of_isobutyryl-CoA_dehydrogenase|not_provided|ACAD8-related_disorder|not_specified": 1,
    "ACAD8-related_disorder|Inborn_genetic_diseases|Deficiency_of_isobutyryl-CoA_dehydrogenase|not_provided": 1,
    "ACAD8-related_disorder": 1,
    "not_provided|not_specified|Deficiency_of_isobutyryl-CoA_dehydrogenase": 1,
    "not_specified|not_provided|IQSEC3-related_disorder": 1,
    "IQSEC3-related_disorder": 2,
    "IQSEC3-related_disorder|not_specified": 1,
    "not_provided|KDM5A-related_disorder": 2,
    "KDM5A-related_disorder": 12,
    "El_Hayek-Chahrour_neurodevelopmental_disorder": 5,
    "not_provided|Intellectual_disability|Seizure": 1,
    "KDM5A-related_Neurodevelopmental_disorder_with_autism": 1,
    "KDM5A-related_disorder|not_provided": 2,
    "El_Hayek-Chahrour_neurodevelopmental_disorder|not_specified": 1,
    "KDM5A-associated_neurodevelopmental_syndrome|El_Hayek-Chahrour_neurodevelopmental_disorder": 1,
    "Pseudohypoaldosteronism_type_2C": 81,
    "Pseudohypoaldosteronism_type_2C|not_provided": 9,
    "Pseudohypoaldosteronism_type_2A|Hereditary_sensory_and_autonomic_neuropathy_type_2": 9,
    "not_provided|Pseudohypoaldosteronism_type_2C": 4,
    "not_provided|Pseudohypoaldosteronism_type_2C|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 1176,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified": 8,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 321,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 18,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 53,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 31,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases": 35,
    "Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided": 23,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 3,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 21,
    "not_provided|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 7,
    "not_provided|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 20,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|WNK1-related_disorder": 3,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 13,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified|not_provided": 6,
    "WNK1-related_disorder": 7,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Charcot-Marie-Tooth_disease": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided|not_specified": 5,
    "not_provided|Pseudohypoaldosteronism_type_2A|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified": 1,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 3,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|WNK1-related_disorder": 1,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Pseudohypoaldosteronism_type_2C|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 5,
    "not_specified|not_provided|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided": 3,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 5,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|WNK1-related_disorder|not_specified|not_provided": 1,
    "WNK1-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 4,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified": 1,
    "Pseudohypoaldosteronism_type_2C|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 3,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Inborn_genetic_diseases": 6,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_provided": 6,
    "See_cases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "not_provided|not_specified|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 4,
    "not_provided|WNK1-related_disorder|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases": 5,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 3,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided|Inborn_genetic_diseases": 7,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|WNK1-related_disorder|Pseudohypoaldosteronism_type_2C": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 4,
    "not_specified|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 2,
    "not_provided|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|WNK1-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified|not_provided": 1,
    "WNK1-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified|WNK1-related_disorder": 1,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided|WNK1-related_disorder": 2,
    "not_specified|WNK1-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided": 1,
    "Hereditary_sensory_and_autonomic_neuropathy_type_2|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Pseudohypoaldosteronism_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Pseudohypoaldosteronism_type_2A|Hereditary_sensory_and_autonomic_neuropathy_type_2|not_provided": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|WNK1-related_disorder": 1,
    "Pseudohypoaldosteronism_type_2C|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "Pseudohypoaldosteronism_type_2C|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "not_specified|not_provided|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 2,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|Inborn_genetic_diseases": 1,
    "Variant_of_unknown_significance|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|WNK1-related_disorder|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided": 1,
    "Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 1,
    "not_provided|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided": 2,
    "not_specified|Pseudohypoaldosteronism_type_2C|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 2,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified|not_provided|Pseudohypoaldosteronism_type_2A|Inborn_genetic_diseases|Hereditary_sensory_and_autonomic_neuropathy_type_2": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|WNK1-related_disorder": 3,
    "Inborn_genetic_diseases|WNK1-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 2,
    "Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_provided": 1,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C": 1,
    "WNK1-related_disorder|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_provided|WNK1-related_disorder|Inborn_genetic_diseases": 1,
    "Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Pseudohypoaldosteronism_type_2A|not_provided|Hereditary_sensory_and_autonomic_neuropathy_type_2|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Inborn_genetic_diseases": 1,
    "Pseudohypoaldosteronism_type_2C|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Pseudohypoaldosteronism_type_2C|Neuropathy|_hereditary_sensory_and_autonomic|_type_2A": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_2A|Pseudohypoaldosteronism_type_2C|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_motor_and_sensory_neuropathy": 2,
    "Hereditary_sensory_and_autonomic_neuropathy_type_2|Pseudohypoaldosteronism_type_2A": 9,
    "Congenital_myasthenic_syndrome_19|RAD52-related_disorder": 1,
    "ERC1-related_disorder": 14,
    "ERC1-related_disorder|not_provided": 1,
    "not_provided|ERC1-related_disorder": 1,
    "not_specified|ERC1-related_disorder": 1,
    "ERC1-related_disorder|not_specified": 1,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation": 36,
    "ADIPOR2-related_disorder": 2,
    "Retinal_cone_dystrophy_4": 57,
    "not_provided|Retinal_cone_dystrophy_4": 33,
    "CACNA2D4-related_disorder|Retinal_cone_dystrophy_4|not_provided": 1,
    "Retinal_cone_dystrophy_4|not_provided": 43,
    "Retinal_cone_dystrophy_4|not_specified|CACNA2D4-related_disorder|not_provided": 1,
    "not_provided|Retinal_cone_dystrophy_4|not_specified": 8,
    "not_specified|not_provided|Retinal_cone_dystrophy_4": 9,
    "not_provided|CACNA2D4-related_disorder": 6,
    "Retinal_cone_dystrophy_4|not_specified|not_provided": 1,
    "not_provided|not_specified|Retinal_cone_dystrophy_4": 6,
    "Retinal_cone_dystrophy_4|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Retinal_cone_dystrophy_4": 2,
    "not_specified|not_provided|Retinal_cone_dystrophy_4|CACNA2D4-related_disorder": 1,
    "Inborn_genetic_diseases|Retinal_cone_dystrophy_4|not_provided": 1,
    "CACNA2D4-related_disorder|not_provided": 3,
    "not_provided|Retinal_cone_dystrophy_4|CACNA2D4-related_disorder": 3,
    "CACNA2D4-related_disorder|not_specified|not_provided|Retinal_cone_dystrophy_4": 1,
    "Retinal_cone_dystrophy_4|CACNA2D4-related_disorder|not_provided": 2,
    "Progressive_cone_dystrophy_(without_rod_involvement)|not_provided|Retinal_cone_dystrophy_4|Cone_dystrophy_3": 1,
    "CACNA2D4-related_disorder|not_specified|Retinal_cone_dystrophy_4|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinal_cone_dystrophy_4": 2,
    "not_provided|CACNA2D4-related_disorder|Retinal_cone_dystrophy_4": 1,
    "Retinal_cone_dystrophy_4|not_provided|not_specified": 2,
    "Retinal_cone_dystrophy_4|Abnormality_of_the_eye|not_provided|CACNA2D4-related_retinopathy": 1,
    "Optic_atrophy|Inborn_genetic_diseases|not_provided|Retinal_cone_dystrophy_4": 1,
    "Retinal_cone_dystrophy_4|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Cone_dystrophy_3|Retinal_cone_dystrophy_4": 1,
    "not_provided|Retinal_dystrophy|Retinal_cone_dystrophy_4": 1,
    "CACNA2D4-related_disorder": 2,
    "Cone_dystrophy_3|not_provided|Inborn_genetic_diseases": 1,
    "CACNA2D4-related_disorder|not_provided|Retinal_cone_dystrophy_4": 1,
    "not_provided|Cone-rod_dystrophy_6|Retinal_dystrophy": 1,
    "Timothy_syndrome|Brugada_syndrome": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 3,
    "Long_QT_syndrome|Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8": 2,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome|See_cases|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|CACNA1C-related_disorder": 10,
    "Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|Long_QT_syndrome|Cardiovascular_phenotype": 6,
    "not_provided|Long_QT_syndrome|Timothy_syndrome": 3,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Timothy_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|not_provided": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_provided|Timothy_syndrome|Brugada_syndrome_3": 1,
    "Long_QT_syndrome|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|not_specified|not_provided|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "Brugada_syndrome|Brugada_syndrome_3": 1,
    "Brugada_syndrome|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|CACNA1C-related_disorder": 2,
    "Long_QT_syndrome|Long_QT_syndrome_8|Timothy_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|CACNA1C-related_disorder": 10,
    "not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_3|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|Timothy_syndrome": 2,
    "not_specified|Long_QT_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3": 3,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|not_provided|Long_QT_syndrome": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|not_specified|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|CACNA1C-related_disorder|Long_QT_syndrome": 4,
    "Long_QT_syndrome|CACNA1C-related_disorder|Cardiovascular_phenotype|not_provided": 3,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Timothy_syndrome|Long_QT_syndrome_8": 2,
    "Long_QT_syndrome|Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|not_provided|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Timothy_syndrome|not_provided|Long_QT_syndrome|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8": 1,
    "not_specified|Brugada_syndrome|Cardiovascular_phenotype|Long_QT_syndrome|Timothy_syndrome": 1,
    "Timothy_syndrome": 15,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures": 30,
    "Timothy_syndrome|not_specified|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Timothy_syndrome|not_provided|not_specified": 1,
    "CACNA1C-related_disorder|Brugada_syndrome_3": 1,
    "Timothy_syndrome|Brugada_syndrome_3|not_provided": 1,
    "CACNA1C-related_disorder": 17,
    "Timothy_syndrome|Brugada_syndrome_3|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome_8": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|CACNA1C-related_disorder": 2,
    "Cardiovascular_phenotype|not_provided|CACNA1C-related_disorder|Long_QT_syndrome": 1,
    "Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_8|Timothy_syndrome|Brugada_syndrome_3": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|CACNA1C-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_8|not_provided": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype|Sudden_cardiac_death|not_provided|Long_QT_syndrome": 1,
    "not_provided|CACNA1C-related_disorder": 5,
    "not_provided|not_specified|Long_QT_syndrome|CACNA1C-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|Long_QT_syndrome_8|Timothy_syndrome|Brugada_syndrome_3|not_provided": 1,
    "Long_QT_syndrome|Timothy_syndrome|not_provided": 9,
    "Cardiovascular_phenotype|Long_QT_syndrome_8|not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|not_provided|Long_QT_syndrome": 1,
    "not_provided|Timothy_syndrome": 6,
    "Timothy_syndrome|Long_QT_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|CACNA1C-related_disorder": 4,
    "not_provided|Timothy_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome_8|Brugada_syndrome_3|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome_8": 8,
    "Brugada_syndrome_3": 2,
    "not_provided|Long_QT_syndrome_8|Timothy_syndrome|Brugada_syndrome_3": 1,
    "not_provided|Inborn_genetic_diseases|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Timothy_syndrome": 2,
    "Long_QT_syndrome_8|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|Timothy_syndrome|Brugada_syndrome_3|CACNA1C-related_disorder": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_provided|Long_QT_syndrome|Wolff-Parkinson-White_pattern": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Brugada_syndrome|Timothy_syndrome": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|CACNA1C-related_disorder|Cardiovascular_phenotype": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Brugada_syndrome_3|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Timothy_syndrome": 1,
    "Concentric_hypertrophic_cardiomyopathy": 1,
    "Timothy_syndrome|Long_QT_syndrome": 5,
    "Long_QT_syndrome_8|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Timothy_syndrome": 1,
    "Long_QT_syndrome_8|Cardiovascular_phenotype|Cardiac_arrhythmia|Long_QT_syndrome|Timothy_syndrome|not_provided|Hypertrophic_cardiomyopathy_1": 1,
    "Long_QT_syndrome_8|Cardiovascular_phenotype|not_provided|Brugada_syndrome_3|Timothy_syndrome|Ventricular_tachycardia|Long_QT_syndrome": 1,
    "Timothy_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_specified|not_provided|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome|not_specified|CACNA1C-related_disorder|Cardiovascular_phenotype": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_provided|Long_QT_syndrome": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "CACNA1C-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome": 3,
    "Timothy_syndrome|Brugada_syndrome_3|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome_8|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|intellectual_deficiency|Epilepsy": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome|Timothy_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Timothy_syndrome|not_provided": 3,
    "Brugada_syndrome_3|Long_QT_syndrome_8": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_specified|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|not_provided|Long_QT_syndrome": 1,
    "not_provided|CACNA1C-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Timothy_syndrome|Hypertrophic_cardiomyopathy|CACNA1C-related_disorder": 1,
    "not_specified|CACNA1C-related_disorder|Long_QT_syndrome_8|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Long_QT_syndrome_8": 4,
    "Timothy_syndrome_type_1": 1,
    "not_provided|Timothy_syndrome|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome_8|Long_QT_syndrome": 2,
    "Long_QT_syndrome_8|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Wolff-Parkinson-White_pattern|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Timothy_syndrome": 1,
    "Long_QT_syndrome|not_provided|Timothy_syndrome": 4,
    "Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|not_provided": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Autism_spectrum_disorder": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Timothy_syndrome|arrhythmogenic_disorders|not_provided": 1,
    "CACNA1C-related_disorder|Long_QT_syndrome": 5,
    "Brugada_syndrome_3|not_provided": 1,
    "Long_QT_syndrome|Timothy_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome_8|Brugada_syndrome_3|not_provided|Cardiovascular_phenotype|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome|Long_QT_syndrome_8|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Timothy_syndrome|Brugada_syndrome_3": 1,
    "not_specified|not_provided|Long_QT_syndrome|CACNA1C-related_disorder|Congestive_heart_failure": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Timothy_syndrome|Long_QT_syndrome": 1,
    "not_provided|Timothy_syndrome|Long_QT_syndrome": 1,
    "Timothy_syndrome|Long_QT_syndrome|not_provided": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome": 1,
    "Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|Long_QT_syndrome": 3,
    "Cardiovascular_phenotype|Sudden_unexplained_death|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|not_provided|Long_QT_syndrome|See_cases": 1,
    "Brugada_syndrome|Long_QT_syndrome|not_provided|Long_QT_syndrome_8|Timothy_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|CACNA1C-related_disorder|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome|Ventricular_tachycardia": 1,
    "Timothy_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8": 2,
    "Inborn_genetic_diseases|Timothy_syndrome|Cardiovascular_phenotype": 1,
    "Timothy_syndrome|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_8|Timothy_syndrome|Brugada_syndrome_3|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|CACNA1C-related_disorder|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cerebral_palsy|Long_QT_syndrome_8|Long_QT_syndrome": 1,
    "Long_QT_syndrome_8|Timothy_syndrome|Brugada_syndrome_3|not_provided": 1,
    "Timothy_syndrome|arrhythmogenic_disorders|QT_prolongation_and_arrhythmias_in_the_absence_of_other_syndromic_features|short_QT_interval_with_or_without_a_Brugada_syndrome_ECG_pattern|Cardiovascular_phenotype|Long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome_8|Brugada_syndrome_3|Short_QT_Syndrome_4": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Long_QT_syndrome|Cardiovascular_phenotype": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|not_specified|Timothy_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|not_specified|not_provided": 1,
    "CACNA1C-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|CACNA1C-related_disorder": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_provided": 1,
    "not_specified|not_provided|Long_QT_syndrome|Intellectual_disability|CACNA1C-related_disorder": 1,
    "CACNA1C-related_disorder|not_provided|Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Hypotonia|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome_8|Long_QT_syndrome|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|not_provided|CACNA1C-related_disorder": 1,
    "Timothy_syndrome|Long_QT_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|not_provided|CACNA1C-related_disorder": 1,
    "Amyloidosis|Long_QT_syndrome": 1,
    "Neurodevelopmental_delay|CACNA1C-related_disorder": 1,
    "Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome": 1,
    "Long_QT_syndrome|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3": 3,
    "CACNA1C-related_disorder|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome|CACNA1C-related_disorder|not_provided|not_specified": 1,
    "not_provided|Long_QT_syndrome|not_specified|Brugada_syndrome|Timothy_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Brugada_syndrome|Timothy_syndrome": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_provided|Long_QT_syndrome": 2,
    "Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Long_QT_syndrome|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_8": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Short_QT_syndrome|Long_QT_syndrome|not_provided": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|CACNA1C-related_disorder|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_provided|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Timothy_syndrome": 1,
    "See_cases|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Timothy_syndrome|CACNA1C-related_disorder": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_specified|not_provided|Long_QT_syndrome": 3,
    "Timothy_syndrome|Brugada_syndrome_3|not_specified|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_8": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|CACNA1C-related_disorder": 2,
    "Long_QT_syndrome|Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|not_provided": 1,
    "Cardiovascular_phenotype|CACNA1C-related_disorder|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Breast_ductal_adenocarcinoma|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Restrictive_cardiomyopathy|Long_QT_syndrome|not_specified|not_provided|Brugada_syndrome|CACNA1C-related_disorder": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_specified|Long_QT_syndrome": 1,
    "Timothy_syndrome|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|Cardiovascular_phenotype|not_provided|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome_8|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "Long_QT_syndrome|CACNA1C-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "CACNA1C-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Long_QT_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Timothy_syndrome|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Timothy_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Brugada_syndrome_3": 1,
    "CACNA1C-related_disorder|not_specified": 1,
    "Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|not_specified|Long_QT_syndrome": 1,
    "not_provided|not_specified|Timothy_syndrome": 1,
    "Timothy_syndrome|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Timothy_syndrome|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|not_specified|CACNA1C-related_disorder|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|CACNA1C-related_disorder|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Long_QT_syndrome|CACNA1C-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Ventricular_tachycardia|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|not_provided": 1,
    "not_provided|not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_provided|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Timothy_syndrome": 1,
    "Long_QT_syndrome_8|Timothy_syndrome|Brugada_syndrome_3|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome": 1,
    "Long_QT_syndrome|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|not_specified|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|not_specified|not_provided|Cardiomyopathy|Long_QT_syndrome": 1,
    "Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_specified|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "CACNA1C-related_disorder|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Brugada_syndrome_3": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures": 1,
    "Cardiovascular_phenotype|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|not_provided|Brugada_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome_8|Cardiovascular_phenotype|Long_QT_syndrome|Timothy_syndrome|Brugada_syndrome_3": 1,
    "Brugada_syndrome_3|Timothy_syndrome|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_3|Timothy_syndrome|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|CACNA1C-related_disorder|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|not_specified": 1,
    "Brugada_syndrome_3|Timothy_syndrome|Long_QT_syndrome_8|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_(shorter-than-normal_QT_interval)|not_specified|Brugada_syndrome|not_provided|Long_QT_syndrome|Timothy_syndrome|Brugada_syndrome_3|CACNA1C-related_disorder": 1,
    "Long_QT_syndrome_8|Brugada_syndrome_3|Timothy_syndrome|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia|Long_QT_syndrome_8|Long_QT_syndrome": 1,
    "not_provided|CACNA1C-related_disorder|Timothy_syndrome|Brugada_syndrome_3|Long_QT_syndrome_8|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Brugada_syndrome|Timothy_syndrome": 5,
    "CACNA1C-related_disorder|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiac_arrhythmia|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Timothy_syndrome|CACNA1C-related_disorder": 1,
    "Timothy_syndrome|Long_QT_syndrome_8|Brugada_syndrome_3|Long_QT_syndrome": 1,
    "Brugada_syndrome_3|Long_QT_syndrome_8|Timothy_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|CACNA1C-related_disorder": 1,
    "CACNA1C-related_disorder|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome|Long_QT_syndrome|Timothy_syndrome": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_language_delay|_and_skeletal_defects_with_or_without_seizures|Long_QT_syndrome": 1,
    "FKBP4-related_disorder": 1,
    "Hepatorenocardiac_degenerative_fibrosis": 8,
    "Hepatorenocardiac_degenerative_fibrosis|not_provided": 1,
    "Inborn_genetic_diseases|Hepatorenocardiac_degenerative_fibrosis": 1,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3": 2,
    "CCND2-related_disorder": 4,
    "not_provided|CCND2-related_disorder": 2,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3": 9,
    "not_specified|CCND2-related_disorder|not_provided": 1,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3|not_specified": 1,
    "CCND2-related_disorder|not_specified": 1,
    "not_provided|CCND2-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3|not_provided": 4,
    "Inborn_genetic_diseases|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3|not_provided": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3|not_provided|Seizure": 1,
    "CCND2-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_3|not_provided": 1,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 19,
    "Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 33,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Autosomal_dominant_hypophosphatemic_rickets": 18,
    "not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Autosomal_dominant_hypophosphatemic_rickets": 8,
    "Familial_hyperphosphatemic_tumoral_calcinosis/hyperphosphatemic_hyperostosis_syndrome|Hypophosphatemic_Rickets|_Dominant": 4,
    "Hypophosphatemic_Rickets|_Dominant|Familial_hyperphosphatemic_tumoral_calcinosis/hyperphosphatemic_hyperostosis_syndrome": 1,
    "Hypophosphatemic_Rickets|_Dominant|not_provided|Familial_hyperphosphatemic_tumoral_calcinosis/hyperphosphatemic_hyperostosis_syndrome": 1,
    "not_provided|Hypophosphatemic_Rickets|_Dominant|Familial_hyperphosphatemic_tumoral_calcinosis/hyperphosphatemic_hyperostosis_syndrome": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 4,
    "Inborn_genetic_diseases|Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|not_specified|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "not_provided|Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 5,
    "Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_provided": 1,
    "FGF23-related_disorder": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_provided": 4,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Autosomal_dominant_hypophosphatemic_rickets|not_provided": 5,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_provided|Autosomal_dominant_hypophosphatemic_rickets": 2,
    "not_provided|Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Inborn_genetic_diseases": 1,
    "Hypophosphatemic_rickets|not_provided|Autosomal_dominant_hypophosphatemic_rickets|Short_stature|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "not_provided|Autosomal_dominant_hypophosphatemic_rickets": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|not_provided": 2,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|FGF23-related_disorder|Autosomal_dominant_hypophosphatemic_rickets|not_provided|not_specified": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_specified|not_provided": 1,
    "Autosomal_dominant_hypophosphatemic_rickets|Inborn_genetic_diseases|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Autosomal_dominant_hypophosphatemic_rickets|not_provided|not_specified": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "Familial_hyperphosphatemic_tumoral_calcinosis/hyperphosphatemic_hyperostosis_syndrome|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Autosomal_dominant_hypophosphatemic_rickets|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 1,
    "not_provided|not_specified|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2|Autosomal_dominant_hypophosphatemic_rickets|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_hypophosphatemic_rickets|Tumoral_calcinosis|_hyperphosphatemic|_familial|_2": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_66": 1,
    "C12orf4-related_disorder": 1,
    "Attention_deficit_hyperactivity_disorder|Hypotonia|Intellectual_disability|Intellectual_disability|_autosomal_recessive_66": 1,
    "Spermatogenic_failure_82": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_26": 10,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_26|not_provided": 2,
    "NDUFA9-related_disorder|not_provided": 3,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_26": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_26|Inborn_genetic_diseases|not_provided|not_specified|Leigh_syndrome": 1,
    "NDUFA9-related_disorder|not_specified|not_provided": 2,
    "NDUFA9-related_disorder": 1,
    "not_provided|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_26": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_26|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_26|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|not_specified|NDUFA9-related_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_26": 1,
    "NDUFA9-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_26|not_specified|not_provided": 1,
    "Pyloric_stenosis|Esophageal_atresia": 1,
    "Focal-onset_seizure|Cerebellar_ataxia|Moderate_global_developmental_delay|Hypermetropia|Pes_planus|Epicanthus|Macrocephaly|Short_philtrum|Generalized-onset_seizure|Atypical_behavior|Inversion_of_nipple": 1,
    "Episodic_ataxia_type_1|not_provided": 13,
    "Myokymia|Episodic_ataxia_type_1": 10,
    "Episodic_ataxia_type_1|Hereditary_episodic_ataxia": 19,
    "Hereditary_episodic_ataxia|Episodic_ataxia_type_1": 20,
    "Episodic_ataxia_type_1|Myokymia": 19,
    "Episodic_ataxia_type_1": 401,
    "Myokymia|Hereditary_episodic_ataxia": 4,
    "not_provided|Episodic_ataxia_type_1": 38,
    "Hereditary_episodic_ataxia|Myokymia": 6,
    "not_provided|Episodic_ataxia_type_1|Myokymia": 2,
    "Episodic_ataxia_type_1|Hereditary_episodic_ataxia|not_provided": 12,
    "not_specified|Episodic_ataxia_type_1": 3,
    "Episodic_ataxia_type_1|Inborn_genetic_diseases": 11,
    "Episodic_ataxia_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Episodic_ataxia_type_1": 7,
    "Inborn_genetic_diseases|not_provided|Episodic_ataxia_type_1": 1,
    "not_specified|not_provided|Episodic_ataxia_type_1": 1,
    "not_provided|not_specified|KCNA1-related_disorder|Inborn_genetic_diseases|Episodic_ataxia_type_1": 1,
    "KCNA1-related_disorder|not_specified|not_provided|Episodic_ataxia_type_1": 1,
    "See_cases|Episodic_ataxia_type_1": 1,
    "Episodic_ataxia_type_1|KCNA1-related_disorder": 1,
    "Episodic_ataxia_type_1|not_specified": 4,
    "Inborn_genetic_diseases|not_specified|Episodic_ataxia_type_1|not_provided": 1,
    "not_specified|KCNA1-related_disorder|Episodic_ataxia_type_1": 1,
    "not_provided|not_specified|Episodic_ataxia_type_1": 1,
    "Myokymia_1": 2,
    "Myokymia|not_specified|Episodic_ataxia_type_1|not_provided": 1,
    "not_provided|Myokymia_1": 1,
    "Myokymia_1_with_hypomagnesemia": 1,
    "not_provided|Hereditary_episodic_ataxia|Episodic_ataxia_type_1|not_specified": 1,
    "not_provided|Episodic_ataxia_type_1|Hereditary_ataxia": 1,
    "KCNA1-related_disorder|Episodic_ataxia_type_1": 3,
    "KCNA1-related_disorder|not_provided|Episodic_ataxia_type_1": 1,
    "Hereditary_episodic_ataxia|not_specified|not_provided|KCNA1-related_disorder|Episodic_ataxia_type_1": 1,
    "Episodic_kinesigenic_dyskinesia|Episodic_ataxia_type_1": 1,
    "not_specified|not_provided|Episodic_ataxia_type_1|Myokymia": 1,
    "KCNA1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Episodic_ataxia_type_1": 1,
    "Episodic_ataxia_type_1|KCNA1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_episodic_ataxia|Myokymia|Episodic_ataxia_type_1": 1,
    "not_specified|not_provided|Myokymia|Episodic_ataxia_type_1": 1,
    "not_specified|Hereditary_episodic_ataxia|Episodic_ataxia_type_1|KCNA1-related_disorder": 1,
    "not_provided|Episodic_ataxia_type_1|Myokymia|not_specified": 1,
    "Myokymia|Episodic_ataxia_type_1|not_provided": 1,
    "Episodic_ataxia_type_1|Myokymia|not_provided": 5,
    "Episodic_ataxia_type_1|not_provided|Hereditary_episodic_ataxia": 2,
    "Hereditary_episodic_ataxia|not_provided|Episodic_ataxia_type_1": 2,
    "not_provided|Myokymia|Episodic_ataxia_type_1": 1,
    "not_provided|Hereditary_episodic_ataxia|Episodic_ataxia_type_1": 1,
    "Atrial_fibrillation|_familial|_7": 362,
    "Atrial_fibrillation|_familial|_7|not_provided": 20,
    "Atrial_fibrillation|_familial|_7|Inborn_genetic_diseases": 18,
    "KCNA5-related_disorder|not_provided|Atrial_fibrillation|_familial|_7": 1,
    "not_provided|Atrial_fibrillation|_familial|_7": 24,
    "not_specified|not_provided|Pulmonary_arterial_hypertension|Atrial_fibrillation|_familial|_7": 1,
    "KCNA5-related_disorder|Atrial_fibrillation|_familial|_7": 3,
    "Inborn_genetic_diseases|Atrial_fibrillation|_familial|_7": 12,
    "not_specified|not_provided|Atrial_fibrillation|_familial|_7": 4,
    "Atrial_fibrillation|_familial|_7|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Atrial_fibrillation|_familial|_7": 2,
    "not_provided|Atrial_fibrillation|_familial|_7|Pulmonary_arterial_hypertension": 2,
    "Atrial_fibrillation|_familial|_7|not_provided|not_specified": 1,
    "Atrial_fibrillation|_familial|_7|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|KCNA5-related_disorder": 1,
    "KCNA5-related_disorder|not_provided|not_specified|Atrial_fibrillation|_familial|_7": 1,
    "KCNA5-related_disorder|not_specified|not_provided|Atrial_fibrillation|_familial|_7|Pulmonary_hypertension|_primary|_1": 1,
    "not_provided|Atrial_fibrillation|_familial|_7|KCNA5-related_disorder": 1,
    "not_provided|not_specified|Atrial_fibrillation|_familial|_7": 1,
    "not_provided|Inborn_genetic_diseases|Atrial_fibrillation|_familial|_7": 1,
    "not_provided|KCNA5-related_disorder|Atrial_fibrillation|_familial|_7": 1,
    "KCNA5-related_disorder|not_provided|not_specified|Pulmonary_arterial_hypertension|Atrial_fibrillation|_familial|_7|altered_potassium_channel_function": 1,
    "KCNA5-related_disorder|not_specified|not_provided|Atrial_fibrillation|_familial|_7": 1,
    "Inborn_genetic_diseases|Atrial_fibrillation|_familial|_7|not_provided": 1,
    "not_specified|Atrial_fibrillation|_familial|_7|not_provided": 1,
    "Third_degree_atrioventricular_block|Atrial_fibrillation|_familial|_7": 1,
    "not_provided|Atrial_fibrillation|_familial|_7|not_specified": 2,
    "Cardiac_arrhythmia|Atrial_fibrillation|_familial|_7": 1,
    "KCNA5-related_disorder": 1,
    "Atrial_fibrillation|_familial|_7|KCNA5-related_disorder|not_provided": 1,
    "Atrial_fibrillation|_familial|_7|not_provided|Heart_disease": 1,
    "Atrial_fibrillation|_familial|_7|Pulmonary_arterial_hypertension": 1,
    "not_specified|not_provided|Atrial_fibrillation|_familial|_7|Brugada_syndrome_1": 1,
    "not_provided|Aganglionic_megacolon": 1,
    "Hereditary_von_Willebrand_disease": 80,
    "VWF-related_disorder|not_provided": 6,
    "von_Willebrand_disease_type_1": 90,
    "not_specified|not_provided|VWF-related_disorder": 2,
    "Hereditary_von_Willebrand_disease|not_specified|not_provided": 3,
    "von_Willebrand_disease_type_3": 95,
    "not_provided|Von_Willebrand_disease_type_2A": 4,
    "Von_Willebrand_disease_type_2A|not_provided": 3,
    "Hereditary_von_Willebrand_disease|not_provided": 15,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1": 1,
    "not_specified|Hereditary_von_Willebrand_disease": 6,
    "not_provided|Hereditary_von_Willebrand_disease": 21,
    "not_provided|von_Willebrand_disease_type_3": 24,
    "Hereditary_von_Willebrand_disease|VWF-related_disorder": 2,
    "not_specified|VWF-related_disorder|not_provided": 1,
    "VWF-related_disorder|not_specified|Hereditary_von_Willebrand_disease": 1,
    "von_Willebrand_disease_type_3|not_provided": 15,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified": 5,
    "Hereditary_von_Willebrand_disease|not_specified|not_provided|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 1,
    "not_provided|VWF-related_disorder": 7,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_specified|not_provided": 2,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided|Hereditary_von_Willebrand_disease|VWF-related_disorder": 1,
    "not_specified|not_provided|Abnormality_of_coagulation|Thrombocytopenia|Abnormal_bleeding|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "Von_Willebrand_disease_type_2B|von_Willebrand_disease_type_1|not_specified": 1,
    "VWF-related_disorder|not_specified|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_provided|Hereditary_von_Willebrand_disease": 1,
    "Hereditary_von_Willebrand_disease|not_specified|not_provided|von_Willebrand_disease_type_1": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided": 2,
    "Abnormality_of_coagulation": 10,
    "Hereditary_von_Willebrand_disease|not_specified|Inborn_genetic_diseases": 1,
    "VWF-related_disorder|not_specified|not_provided": 4,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_3": 2,
    "von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_2": 42,
    "von_Willebrand_disorder|not_provided|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disease_type_2|not_specified": 1,
    "not_specified|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided": 2,
    "von_Willebrand_disorder|von_Willebrand_disease_type_3|not_provided": 1,
    "VWF-related_disorder": 30,
    "not_provided|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 2,
    "not_provided|not_specified|VWF-related_disorder": 3,
    "not_provided|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2": 1,
    "von_Willebrand_disease_type_1|not_provided": 7,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disorder|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1": 5,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 3,
    "Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_1|VWF-related_disorder|not_specified": 1,
    "von_Willebrand_disorder|VWF-related_disorder|not_provided": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3": 3,
    "not_provided|von_Willebrand_disease_type_2": 8,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disorder|not_provided|Hereditary_von_Willebrand_disease|Thrombocytopenia|Abnormal_bleeding": 1,
    "von_Willebrand_disorder": 9,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_specified|not_provided": 3,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_specified": 1,
    "VWF-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_specified|not_provided": 4,
    "not_provided|Hereditary_von_Willebrand_disease|not_specified|von_Willebrand_disease_type_3": 1,
    "VWF-related_disorder|not_specified": 2,
    "Abnormality_of_coagulation|von_Willebrand_disease_type_1": 1,
    "VWF-related_disorder|not_provided|not_specified": 4,
    "Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified": 2,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|not_provided": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_provided|not_specified": 3,
    "Hereditary_von_Willebrand_disease|not_specified": 1,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified|not_provided|Hereditary_von_Willebrand_disease": 1,
    "not_specified|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_provided": 3,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_specified": 6,
    "Hereditary_von_Willebrand_disease|VWF-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_von_Willebrand_disease|VWF-related_disorder|not_provided": 1,
    "not_specified|Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 1,
    "not_provided|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease|Abnormality_of_coagulation|von_Willebrand_disease_type_1": 1,
    "not_provided|von_Willebrand_disease_type_1": 10,
    "von_Willebrand_disease_type_1|Abnormality_of_coagulation|not_provided": 1,
    "VWF-related_disorder|not_provided|Abnormal_bleeding|Thrombocytopenia": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 4,
    "Inborn_genetic_diseases|VWF-related_disorder": 1,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 2,
    "Hereditary_von_Willebrand_disease|Inborn_genetic_diseases": 1,
    "von_Willebrand_disease_type_1|not_specified|Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2": 7,
    "not_specified|not_provided|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2": 5,
    "von_Willebrand_disease_type_3|Abnormality_of_coagulation|von_Willebrand_disease_type_1|not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 1,
    "not_provided|Hereditary_von_Willebrand_disease|not_specified": 3,
    "von_Willebrand_disease_type_1|Hereditary_von_Willebrand_disease|See_cases": 1,
    "Inborn_genetic_diseases|von_Willebrand_disease_type_1": 2,
    "Inborn_genetic_diseases|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_provided": 1,
    "VWF-related_disorder|Hereditary_von_Willebrand_disease|Abnormality_of_blood_and_blood-forming_tissues|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease": 2,
    "not_provided|Inborn_genetic_diseases|von_Willebrand_disease_type_2": 1,
    "not_provided|not_specified|von_Willebrand_disease_type_2": 1,
    "von_Willebrand_disease_type_2M": 4,
    "von_Willebrand_disorder|not_provided|VWF-related_disorder|See_cases|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disease_type_3|not_specified|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disease_type_2": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|VWF-related_disorder|not_specified|not_provided|Hereditary_von_Willebrand_disease|Abnormality_of_coagulation": 1,
    "not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_2M": 1,
    "von_Willebrand_disease_type_1|VWF-related_disorder": 1,
    "not_provided|von_Willebrand_disorder": 4,
    "VWF-related_disorder|not_specified|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided|Hereditary_von_Willebrand_disease": 1,
    "not_specified|von_Willebrand_disease_type_1": 3,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "not_specified|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3": 1,
    "VWF-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 2,
    "von_Willebrand_disease_type_1|Hereditary_von_Willebrand_disease": 1,
    "not_provided|not_specified|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_2|not_specified|not_provided": 2,
    "von_Willebrand_disease_type_2|not_provided": 10,
    "VWF-related_disorder|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disease_type_3": 1,
    "Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_2": 4,
    "VWF-related_disorder|von_Willebrand_disorder|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|Von_Willebrand_disease_type_2A": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|Inborn_genetic_diseases": 1,
    "Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_2": 1,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided": 1,
    "Von_Willebrand_disease_type_2A|not_provided|von_Willebrand_disease_type_2": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 2,
    "Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Thrombus|von_Willebrand_disorder|VWF-related_disorder|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|Inborn_genetic_diseases|Hereditary_von_Willebrand_disease|not_provided|.|Thrombocytopenia": 1,
    "not_specified|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided": 1,
    "Inborn_genetic_diseases|VWF-related_disorder|von_Willebrand_disease_type_2|not_specified": 1,
    "Hereditary_von_Willebrand_disease|not_specified|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_provided": 1,
    "not_specified|not_provided|von_Willebrand_disease_type_2": 2,
    "Von_Willebrand_disease_type_2A": 2,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|not_provided": 3,
    "not_provided|Von_Willebrand_disease_type_2A|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 1,
    "not_specified|von_Willebrand_disease_type_2": 2,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|not_specified|not_provided": 1,
    "Abnormality_of_coagulation|not_provided": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified|not_provided|von_Willebrand_disease_type_2": 2,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_2M|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|not_provided": 1,
    "von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2M": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 1,
    "not_provided|Inborn_genetic_diseases|VWF-related_disorder": 1,
    "von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|not_specified": 1,
    "von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease|not_provided": 2,
    "von_Willebrand_disease_type_2M|not_provided": 2,
    "not_specified|Von_Willebrand_disease_type_2A|not_provided": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_2M|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|VWF-related_disorder|not_provided": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|VWF-related_disorder|not_provided|not_specified|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|Abnormality_of_coagulation": 1,
    "von_Willebrand_disease_type_2M|von_Willebrand_disorder|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 1,
    "not_provided|Hereditary_von_Willebrand_disease|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|not_specified": 2,
    "Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "VWF-related_disorder|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease": 1,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 2,
    "von_Willebrand_disease_type_1|Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_2M|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|Prolonged_bleeding_time|Abnormal_bleeding": 1,
    "von_Willebrand_disorder|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 1,
    "von_Willebrand_disease_type_1|not_provided|Hereditary_von_Willebrand_disease": 1,
    "not_specified|not_provided|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease": 1,
    "VWF-related_disorder|not_provided|Von_Willebrand_disease_type_2B|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disease_type_2": 1,
    "not_provided|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 3,
    "Hereditary_von_Willebrand_disease|not_specified|von_Willebrand_disease_type_3": 1,
    "not_provided|von_Willebrand_disease_type_2M": 1,
    "von_Willebrand_disease_type_2|not_provided|von_Willebrand_disease_type_2M": 1,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|Hereditary_von_Willebrand_disease|not_provided|Von_Willebrand_disease_type_2B": 1,
    "von_Willebrand_disease_type_1|Inborn_genetic_diseases|von_Willebrand_disease_type_2|von_Willebrand_disease_type_2M|not_provided": 1,
    "not_provided|von_Willebrand_disorder|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|VWF-related_disorder": 1,
    "Von_Willebrand_disease_type_2B|not_provided": 3,
    "not_provided|Von_Willebrand_disease_type_2B": 1,
    "Thrombocytopenia|Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_3": 1,
    "Von_Willebrand_disease_type_2B|not_provided|von_Willebrand_disease_type_1": 1,
    "Hereditary_von_Willebrand_disease|Von_Willebrand_disease_type_2B": 1,
    "Von_Willebrand_disease_type_2B|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|not_provided": 1,
    "not_provided|Von_Willebrand_disease_type_2B|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease": 1,
    "not_provided|von_Willebrand_disease_type_2|VWF-related_disorder": 1,
    "Hereditary_von_Willebrand_disease|Von_Willebrand_disease_type_2B|not_provided|Abnormality_of_coagulation|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "not_provided|von_Willebrand_disease_type_1|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2": 1,
    "Von_Willebrand_disease_type_2B|von_Willebrand_disease_type_2|not_provided": 1,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_1|not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|Thrombocytopenia": 1,
    "not_provided|von_Willebrand_disease_type_2|Von_Willebrand_disease_type_2A": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|Von_Willebrand_disease_type_2B|not_provided": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|VWF-related_disorder|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|Thrombocytopenia|Von_Willebrand_disease_type_2B": 1,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_specified|VWF-related_disorder|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|Hereditary_von_Willebrand_disease": 1,
    "von_Willebrand_disease_type_2|not_specified|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_provided": 1,
    "VWF-related_disorder|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|not_specified": 1,
    "not_specified|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2": 1,
    "not_specified|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_provided": 1,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|Abnormality_of_coagulation": 1,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|Abnormality_of_coagulation": 1,
    "VWF-related_disorder|Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_1|von_Willebrand_factor_Vicenza|Reduced_von_Willebrand_factor_activity|Reduced_quantity_of_Von_Willebrand_factor": 1,
    "von_Willebrand_disorder|not_provided|Hereditary_von_Willebrand_disease": 1,
    "not_provided|not_specified|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|Inborn_genetic_diseases": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|not_specified|not_provided": 1,
    "not_specified|Reduced_von_Willebrand_factor_activity|Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 1,
    "Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_1|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3": 1,
    "Von_Willebrand_disease_type_2A|Hereditary_von_Willebrand_disease|not_provided": 1,
    "von_Willebrand_disease_type_1|not_provided|not_specified|Hereditary_von_Willebrand_disease": 1,
    "von_Willebrand_disorder|von_Willebrand_disease_type_3|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_1|Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_2|not_provided": 1,
    "Von_Willebrand_disease_type_2A|von_Willebrand_disease_type_1|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|not_provided|not_specified": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|not_specified": 1,
    "not_provided|von_Willebrand_disease_type_2|von_Willebrand_disorder|von_Willebrand_disease_type_1": 1,
    "not_provided|Hereditary_von_Willebrand_disease|not_specified|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "not_provided|Abnormal_bleeding|Thrombocytopenia|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "not_provided|not_specified|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_2N|not_provided": 3,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_3|not_specified|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|von_Willebrand_disease_type_1": 1,
    "not_provided|Hereditary_von_Willebrand_disease|not_specified|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2": 1,
    "Hereditary_von_Willebrand_disease|not_provided|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_specified": 1,
    "not_provided|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disease_type_2N": 1,
    "not_provided|von_Willebrand_disease_type_2N": 2,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease": 1,
    "von_Willebrand_disorder|VWF-related_disorder|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2N|Thrombocytopenia|Abnormal_bleeding|Abnormality_of_coagulation": 1,
    "not_provided|Thrombocytopenia|Abnormal_bleeding|von_Willebrand_disease_type_3": 1,
    "not_specified|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2": 1,
    "not_provided|Abnormality_of_coagulation": 2,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2N": 1,
    "VWF-related_disorder|von_Willebrand_disease_type_1|von_Willebrand_disorder|not_provided": 1,
    "von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided|Hereditary_von_Willebrand_disease|Abnormal_bleeding": 1,
    "not_provided|von_Willebrand_disease_type_2N|not_specified|Abnormal_bleeding": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided": 2,
    "von_Willebrand_disease_type_2N|von_Willebrand_disease_type_2|Abnormal_bleeding|Hereditary_von_Willebrand_disease|not_provided": 1,
    "not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|not_specified|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "VWF-related_disorder|not_provided|von_Willebrand_disease_type_3": 1,
    "Hereditary_factor_VIII_deficiency_disease": 488,
    "von_Willebrand_disease_type_1|Inborn_genetic_diseases": 2,
    "not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|not_specified": 1,
    "not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_2N|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "Inborn_genetic_diseases|not_provided|VWF-related_disorder": 1,
    "von_Willebrand_disease_type_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Hereditary_von_Willebrand_disease|not_provided": 1,
    "Hemorrhage|not_provided|not_specified|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|Hereditary_von_Willebrand_disease": 1,
    "Abnormal_bleeding|not_provided": 1,
    "not_specified|VWF-related_disorder": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3|not_provided|not_specified|VWF-related_disorder": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3": 1,
    "not_specified|von_Willebrand_disease_type_1|not_provided": 2,
    "VWF-related_disorder|not_provided|von_Willebrand_disease_type_2": 1,
    "not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified|not_provided": 4,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|von_Willebrand_disease_type_2|VWF-related_disorder|not_specified|not_provided|von_Willebrand_disease_type_3": 1,
    "not_provided|not_specified|VWF-related_disorder|Hereditary_von_Willebrand_disease": 1,
    "von_Willebrand_disease_type_2|Von_Willebrand_disease_type_2A|not_provided": 1,
    "not_specified|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|not_provided": 1,
    "von_Willebrand_disease_type_2|Inborn_genetic_diseases": 1,
    "not_provided|VWF-related_disorder|not_specified": 1,
    "VWF-related_disorder|Hereditary_von_Willebrand_disease": 1,
    "VWF-related_disorder|Hereditary_von_Willebrand_disease|not_provided": 1,
    "Inborn_genetic_diseases|von_Willebrand_disease_type_2": 1,
    "not_specified|Inborn_genetic_diseases|VWF-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|von_Willebrand_disorder": 1,
    "not_provided|VWF-related_disorder|von_Willebrand_disease_type_3": 1,
    "not_specified|not_provided|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disorder|not_provided|Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|von_Willebrand_disease_type_1": 1,
    "not_specified|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|Hereditary_von_Willebrand_disease|not_provided": 1,
    "not_provided|not_specified|Hereditary_von_Willebrand_disease": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|von_Willebrand_disease_type_2|not_specified": 1,
    "Hereditary_von_Willebrand_disease|not_provided|VWF-related_disorder|von_Willebrand_disease_type_1": 1,
    "von_Willebrand_disease_type_1|VWF-related_disorder|not_provided": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_3|Reduced_quantity_of_Von_Willebrand_factor|Reduced_von_Willebrand_factor_activity|von_Willebrand_disease_type_1|not_provided|not_specified": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_2|von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_provided|not_specified": 1,
    "Von_Willebrand_disease_type_2B": 1,
    "not_specified|von_Willebrand_disease_type_2|not_provided|von_Willebrand_disease_type_1": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disease_type_1|not_provided": 1,
    "Hereditary_von_Willebrand_disease|not_specified|von_Willebrand_disease_type_1|not_provided": 1,
    "von_Willebrand_disease_type_1|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "von_Willebrand_disease_type_3|von_Willebrand_disorder": 1,
    "VWF-related_disorder|not_specified|not_provided|Hereditary_von_Willebrand_disease": 1,
    "VWF-related_disorder|von_Willebrand_disease_type_1|not_provided|von_Willebrand_disease_type_2|von_Willebrand_disease_type_3": 1,
    "von_Willebrand_disease_type_1|von_Willebrand_disease_type_3|not_specified|not_provided": 1,
    "Hereditary_von_Willebrand_disease|von_Willebrand_disorder|VWF-related_disorder|not_provided": 1,
    "PLEKHG6-related_disorder": 3,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 355,
    "Familial_Periodic_Fever": 3,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_provided": 19,
    "not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 30,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Inborn_genetic_diseases": 5,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Autoinflammatory_syndrome": 5,
    "Autoinflammatory_syndrome|not_specified|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 2,
    "See_cases|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "Autoinflammatory_syndrome|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 6,
    "TNFRSF1A-related_disorder": 11,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Autoinflammatory_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 4,
    "not_provided|TNFRSF1A-related_disorder|Autoinflammatory_syndrome|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "Autoinflammatory_syndrome|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_provided": 2,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|TNFRSF1A-related_disorder": 4,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_specified": 4,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Autoinflammatory_syndrome|not_provided": 2,
    "not_specified|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 7,
    "not_provided|Inborn_genetic_diseases|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "Autoinflammatory_syndrome|TNFRSF1A-related_disorder|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 2,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|TNFRSF1A-related_disorder|not_provided|not_specified": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Behcet_disease|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "not_provided|TNFRSF1A-related_disorder|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Autoinflammatory_syndrome|TNFRSF1A-related_disorder": 2,
    "not_provided|not_specified|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 2,
    "not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Autoinflammatory_syndrome": 1,
    "TNFRSF1A-related_disorder|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_specified": 1,
    "not_provided|Autoinflammatory_syndrome": 5,
    "Autoinflammatory_syndrome|Associated_with_severe_COVID-19_disease|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_specified|not_provided|Multiple_sclerosis|_susceptibility_to|_5|Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_plasma_levels_of_TNF|_TNFR|_and/or_TNFR6|Susceptibility_to_severe_coronavirus_disease_(COVID-19)": 1,
    "Behcet_disease|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "TNFRSF1A-related_disorder|not_provided": 1,
    "not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_specified": 3,
    "not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Multiple_sclerosis|_susceptibility_to|_5": 1,
    "Hepatosplenomegaly|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Autoinflammatory_syndrome|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "Autoinflammatory_syndrome|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "Autoinflammatory_syndrome|TNFRSF1A-related_disorder|Inborn_genetic_diseases|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 2,
    "Autoinflammatory_syndrome|Multiple_sclerosis|_susceptibility_to|_5|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_specified|not_provided": 1,
    "not_specified|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Autoinflammatory_syndrome": 1,
    "not_specified|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|TNFRSF1A-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "Multiple_sclerosis|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "not_provided|TNFRSF1A-related_disorder": 1,
    "TNFRSF1A-related_disorder|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "not_specified|not_provided|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)": 1,
    "TNFRSF1A-related_disorder|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|not_provided": 1,
    "not_specified|not_provided|Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_plasma_levels_of_TNF|_TNFR|_and/or_TNFR7|Associated_with_severe_COVID-19_disease|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Susceptibility_to_severe_coronavirus_disease_(COVID-19)": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Familial_Periodic_Fever": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Familial_Periodic_Fever|Autoinflammatory_syndrome": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|TNF_receptor-associated_periodic_fever_syndrome_(TRAPS)|Familial_Periodic_Fever": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 25,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Familial_Periodic_Fever": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided": 9,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 17,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 6,
    "SCNN1A-related_disorder": 5,
    "Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 79,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3": 3,
    "Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 3,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 2,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|SCNN1A-related_disorder": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 5,
    "Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Inborn_genetic_diseases": 5,
    "Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Inborn_genetic_diseases": 3,
    "not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3": 1,
    "Liddle_syndrome_3|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided|not_specified": 3,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Liddle_syndrome_3": 1,
    "not_provided|Incidental_Discovery|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|SCNN1A-related_disorder": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 3,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 2,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|not_specified": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "SCNN1A-related_disorder|not_provided": 3,
    "Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 3,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_specified": 2,
    "not_provided|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 2,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|not_specified": 1,
    "Idiopathic_bronchiectasis": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|not_provided": 2,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3": 1,
    "Inborn_genetic_diseases|Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 4,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|Pseudohypoaldosteronism": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|not_provided": 1,
    "not_provided|not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_3": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Inborn_genetic_diseases": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided": 1,
    "Inborn_genetic_diseases|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Inborn_genetic_diseases": 1,
    "not_provided|Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Inborn_genetic_diseases": 1,
    "not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "Liddle_syndrome_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided|SCNN1A-related_disorder|not_specified": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|not_provided|SCNN1A-related_disorder|not_specified": 1,
    "SCNN1A-related_disorder|not_specified|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Liddle_syndrome_3": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 2,
    "Lymphoproliferative_syndrome_2": 162,
    "Lymphoproliferative_syndrome_2|Inborn_genetic_diseases": 8,
    "Autoinflammatory_syndrome|Lymphoproliferative_syndrome_2|CD27-related_disorder|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|Lymphoproliferative_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|Lymphoproliferative_syndrome_2": 7,
    "CD27-related_disorder": 1,
    "Lymphoproliferative_syndrome_2|not_provided": 9,
    "not_specified|Lymphoproliferative_syndrome_2|not_provided": 2,
    "Combined_immunodeficiency|Immunodeficiency": 1,
    "Autoinflammatory_syndrome|Lymphoproliferative_syndrome_2": 2,
    "Combined_immunodeficiency|Immunodeficiency|Lymphoproliferative_syndrome_2": 1,
    "not_provided|Lymphoproliferative_syndrome_2": 2,
    "not_specified|Lymphoproliferative_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Lymphoproliferative_syndrome_2|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Lymphoproliferative_syndrome_2": 2,
    "Autoinflammatory_syndrome|Lymphoproliferative_syndrome_2|CD27-related_disorder": 1,
    "Lymphoproliferative_syndrome_2|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Lymphoproliferative_syndrome_2": 1,
    "Spastic_ataxia_1|Myasthenic_syndrome|_congenital|_25|_presynaptic|not_provided": 1,
    "Spastic_paraplegia|Myasthenic_syndrome|_congenital|_25|_presynaptic": 2,
    "Myasthenic_syndrome|_congenital|_25|_presynaptic": 3,
    "not_provided|Spastic_paraplegia|Spastic_ataxia_1|Myasthenic_syndrome|_congenital|_25|_presynaptic": 1,
    "not_provided|VAMP1-related_disorder|Myasthenic_syndrome|_congenital|_25|_presynaptic|Spastic_paraplegia|Spastic_ataxia_1": 1,
    "not_specified|Spastic_ataxia_1|Myasthenic_syndrome|_congenital|_25|_presynaptic|not_provided|Spastic_paraplegia": 1,
    "VAMP1-related_disorder": 1,
    "Spastic_ataxia_1": 1,
    "Congenital_myasthenic_syndrome|Myasthenic_syndrome|_congenital|_25|_presynaptic|Spastic_paraplegia": 1,
    "Spastic_ataxia_1|not_provided|Myasthenic_syndrome|_congenital|_25|_presynaptic": 1,
    "Houge-Janssens_syndrome_2|Myasthenic_syndrome|_congenital|_25|_presynaptic": 1,
    "Spastic_paraplegia|Spastic_ataxia_1": 1,
    "NCAPD2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|NCAPD2-related_disorder": 1,
    "not_provided|Microcephaly_21|_primary|_autosomal_recessive": 8,
    "NCAPD2-related_disorder": 11,
    "Microcephaly_21|_primary|_autosomal_recessive": 7,
    "Microcephaly_21|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NCAPD2-related_disorder|not_provided": 1,
    "NCAPD2-related_disorder|not_provided": 5,
    "not_provided|NCAPD2-related_disorder": 3,
    "Microcephaly_21|_primary|_autosomal_recessive|not_provided": 2,
    "Sifrim-Hitz-Weiss_syndrome": 76,
    "CHD4-related_disorder": 29,
    "Moyamoya_angiopathy_with_developmental_delay|Sifrim-Hitz-Weiss_syndrome": 1,
    "CHD4-related_disorder|not_provided": 12,
    "Sifrim-Hitz-Weiss_syndrome|not_provided": 9,
    "Sifrim-Hitz-Weiss_syndrome|not_provided|CHD4-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|CHD4-related_disorder": 1,
    "CHD4-related_disorder|Moyamoya_angiopathy_with_developmental_delay": 1,
    "Inborn_genetic_diseases|CHD4-related_disorder": 1,
    "Sifrim-Hitz-Weiss_syndrome|not_provided|CHD4-related_disorder": 1,
    "not_provided|CHD4-related_disorder": 14,
    "Sifrim-Hitz-Weiss_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Sifrim-Hitz-Weiss_syndrome": 9,
    "Sifrim-Hitz-Weiss_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CHD4-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|CHD4-related_disorder": 1,
    "CHD4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CHD4-related_disorder|not_specified": 1,
    "Thalidomide_response|not_provided|Sifrim-Hitz-Weiss_syndrome": 1,
    "Sifrim-Hitz-Weiss_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "CHD4-related_disorder|Cleft_palate": 1,
    "Neoplasm_of_brain": 1,
    "Immunodeficiency_79": 2,
    "not_specified|Immunodeficiency_79": 1,
    "not_provided|Immunodeficiency_79|not_specified": 3,
    "CD4-related_disorder|not_specified": 1,
    "CD4-related_disorder|not_provided": 1,
    "not_provided|not_specified|CD4-related_disorder|Okt4_epitope_deficiency": 1,
    "Okt4_epitope_deficiency|Immunodeficiency_79": 1,
    "CD4-related_disorder": 2,
    "Immunodeficiency_79|Okt4_epitope_deficiency|not_specified": 1,
    "Immunodeficiency_79|not_provided": 1,
    "Immunodeficiency_79|not_specified|not_provided": 2,
    "Congenital_stationary_night_blindness_1H": 2,
    "Congenital_stationary_night_blindness_1H|Retinal_dystrophy|not_provided": 1,
    "not_provided|GNB3-related_condition": 1,
    "GNB3-related_condition|not_provided": 1,
    "Congenital_stationary_night_blindness_1H|Essential_hypertension|_genetic|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypertension|_essential|_susceptibility_to|Congenital_stationary_night_blindness_1H|GNB3-related_condition|GNB3_POLYMORPHISM": 1,
    "not_provided|Triosephosphate_isomerase_deficiency": 17,
    "Triosephosphate_isomerase_deficiency|not_provided": 9,
    "Triosephosphate_isomerase_deficiency": 48,
    "TPI1-related_disorder": 2,
    "Triosephosphate_isomerase_deficiency|TPI1-related_disorder": 1,
    "Triosephosphate_isomerase_deficiency|not_provided|TPI1-related_disorder": 1,
    "not_provided|Triosephosphate_isomerase_manchester": 1,
    "Triosephosphate_isomerase_deficiency|Inborn_genetic_diseases": 2,
    "Triosephosphate_isomerase_deficiency|not_provided|not_specified": 1,
    "TPI1-related_disorder|not_provided|Triosephosphate_isomerase_deficiency": 1,
    "Inborn_genetic_diseases|Triosephosphate_isomerase_deficiency|not_provided": 1,
    "Triosephosphate_isomerase_deficiency|TPI1-related_disorder|not_provided": 1,
    "not_provided|Triosephosphate_isomerase_deficiency|Inborn_genetic_diseases": 1,
    "Spermatogenic_failure_92": 2,
    "ENO2-related_disorder": 2,
    "ATN1-related_disorder": 11,
    "not_provided|ATN1-related_disorder": 3,
    "Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 10,
    "ATN1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|ATN1-related_disorder": 2,
    "Inborn_genetic_diseases|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|not_provided": 1,
    "Inborn_genetic_diseases|ATN1-related_disorder|not_provided": 1,
    "not_provided|ATN1-related_disorder|not_specified|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|Dentatorubral-pallidoluysian_atrophy": 1,
    "Dentatorubral-pallidoluysian_atrophy|not_specified|not_provided": 1,
    "Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|Dentatorubral-pallidoluysian_atrophy|not_provided": 1,
    "not_specified|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "ATN1-related_disorder|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|not_specified": 2,
    "ATN1-related_disorder|Dentatorubral-pallidoluysian_atrophy|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|not_specified|not_provided": 1,
    "ATN1-related_disorder|See_cases": 1,
    "Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|Dentatorubral-pallidoluysian_atrophy": 1,
    "not_provided|Dentatorubral-pallidoluysian_atrophy|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 1,
    "Dentatorubral-pallidoluysian_atrophy|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 1,
    "X-linked_hydrocephalus_syndrome": 34,
    "Inborn_genetic_diseases|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 2,
    "Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|Dentatorubral-pallidoluysian_atrophy|Inborn_genetic_diseases": 1,
    "Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|not_provided": 3,
    "Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|Congenital_ATN1_related_disorder": 2,
    "ATN1-related_disorder|Congenital_ATN1_related_disorder|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 1,
    "Dentatorubral-pallidoluysian_atrophy|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies|not_provided": 1,
    "ATN1-related_disorder|not_provided|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 1,
    "not_provided|Congenital_hypotonia|_epilepsy|_developmental_delay|_and_digital_anomalies": 1,
    "Congenital_ATN1_related_disorder": 1,
    "C12orf57-related_disorder": 3,
    "Aicardi-Goutieres_syndrome_9": 2,
    "Aicardi-Goutieres_syndrome_9|not_provided": 3,
    "not_provided|Spasticity|Aicardi-Goutieres_syndrome_9": 1,
    "Spasticity|Aicardi-Goutieres_syndrome_9": 1,
    "not_specified|Aicardi-Goutieres_syndrome_9": 1,
    "Temtamy_syndrome": 180,
    "not_provided|not_specified|C12orf57-related_disorder": 1,
    "C12orf57-related_disorder|not_provided|not_specified": 1,
    "Temtamy_syndrome|not_provided|Seizure|Microphthalmia|_isolated|_with_coloboma|Abnormal_corpus_callosum_morphology|Global_developmental_delay": 1,
    "not_provided|Temtamy_syndrome": 4,
    "Temtamy_syndrome|not_provided": 7,
    "C12orf57-related_disorder|Temtamy_syndrome|not_provided": 1,
    "Temtamy_syndrome|C12orf57-related_disorder": 1,
    "not_provided|Temtamy_syndrome|C12orf57-related_disorder": 1,
    "C12orf57-related_disorder|not_specified|Temtamy_syndrome": 1,
    "Temtamy_syndrome|not_provided|Inborn_genetic_diseases|C12orf57-related_disorder": 1,
    "Inborn_genetic_diseases|Temtamy_syndrome": 3,
    "Temtamy_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Temtamy_syndrome": 3,
    "Temtamy_syndrome|Vesicoureteral_reflux|Intellectual_disability|Attention_deficit_hyperactivity_disorder|Renal_atrophy|Hydronephrosis|Global_developmental_delay": 1,
    "Temtamy_syndrome|C12orf57-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|C12orf57-related_disorder|Temtamy_syndrome": 1,
    "not_provided|Temtamy_syndrome|not_specified": 1,
    "not_specified|not_provided|Temtamy_syndrome": 1,
    "Intellectual_disability|not_provided|Temtamy_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Temtamy_syndrome": 1,
    "EMG1-related_disorder": 3,
    "Bowen-Conradi_syndrome|not_provided": 1,
    "Bowen-Conradi_syndrome": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_2": 3,
    "not_provided|not_specified|Complement_component_C1s_deficiency|Ehlers-Danlos_syndrome|_periodontal_type_2": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|Inborn_genetic_diseases|not_provided": 1,
    "C1S-related_disorder|not_provided": 10,
    "not_provided|C1S-related_disorder": 5,
    "Complement_component_C1s_deficiency|not_provided": 2,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_periodontal_type_2": 3,
    "C1S-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Complement_component_C1s_deficiency|Ehlers-Danlos_syndrome|_periodontal_type_2|not_provided": 2,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|Complement_component_C1s_deficiency|not_specified|not_provided": 2,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|not_provided": 2,
    "C1S-related_disorder": 4,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|Ehlers-Danlos_syndrome|_periodontal_type_1": 7,
    "not_provided|Complement_component_C1s_deficiency|Ehlers-Danlos_syndrome|_periodontal_type_2|not_specified": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_1|Ehlers-Danlos_syndrome|_periodontal_type_2": 9,
    "Complement_component_C1s_deficiency|Ehlers-Danlos_syndrome|_periodontal_type_2|not_provided|C1S-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|Complement_component_C1s_deficiency|not_provided": 2,
    "C1S-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|C1S-related_disorder|not_specified|not_provided": 1,
    "Complement_component_C1s_deficiency": 3,
    "not_provided|Inborn_genetic_diseases|Complement_component_C1s_deficiency|Ehlers-Danlos_syndrome|_periodontal_type_2": 1,
    "not_provided|C1S-related_disorder|Inborn_genetic_diseases": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_2|not_provided|Complement_component_C1s_deficiency": 1,
    "C1R-related_disorder": 6,
    "Ehlers-Danlos_syndrome|_periodontal_type_1": 12,
    "not_specified|C1R-related_disorder": 3,
    "C1R-related_disorder|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_1|not_specified": 1,
    "not_specified|not_provided|Ehlers-Danlos_syndrome|_periodontal_type_1": 1,
    "C1R-related_disorder|Ehlers-Danlos_syndrome|_periodontal_type_1": 1,
    "not_specified|C1R-related_disorder|not_provided": 1,
    "not_provided|Ehlers-Danlos_syndrome|_periodontal_type_1|not_specified|Vascular_dementia": 1,
    "Ehlers-Danlos_syndrome|_periodontal_type_1|not_specified|not_provided": 1,
    "not_provided|C1R-related_disorder": 2,
    "C1R-related_disorder|not_specified": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)": 49,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided": 9,
    "PEX5-related_disorder": 8,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|PEX5-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases": 24,
    "not_provided|Peroxisome_biogenesis_disorder_2B": 20,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2B": 17,
    "Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder|not_provided": 1,
    "PEX5-related_disorder|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B": 2,
    "Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder": 9,
    "PEX5-related_disorder|not_provided|Peroxisome_biogenesis_disorder_2B": 3,
    "Fanconi_anemia_complementation_group_D2|Rhizomelic_chondrodysplasia_punctata_type_5": 1,
    "Peroxisome_biogenesis_disorder_2B|Rhizomelic_chondrodysplasia_punctata_type_5|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 2,
    "Peroxisome_biogenesis_disorder_2B|Rhizomelic_chondrodysplasia_punctata_type_5|not_specified|Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided": 1,
    "not_provided|PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B": 2,
    "Peroxisome_biogenesis_disorder_due_to_PEX5_defect": 2,
    "Rhizomelic_chondrodysplasia_punctata_type_5|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B": 1,
    "PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B": 13,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2B|not_provided": 5,
    "Peroxisome_biogenesis_disorder_2B|Rhizomelic_chondrodysplasia_punctata_type_5|Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases|not_provided": 3,
    "Peroxisome_biogenesis_disorder_2B|not_specified|not_provided|PEX5-related_disorder|Inborn_genetic_diseases": 1,
    "PEX5-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B": 1,
    "PEX5-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2B|not_provided": 24,
    "not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|Rhizomelic_chondrodysplasia_punctata_type_5": 4,
    "not_provided|PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "PEX5-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder": 2,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|not_provided|Rhizomelic_chondrodysplasia_punctata_type_5": 2,
    "not_provided|Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases": 2,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)|PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|not_provided": 2,
    "PEX5-related_disorder|not_specified|not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)|PEX5-related_disorder": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_5|Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_2B|not_provided|Inborn_genetic_diseases": 2,
    "Abnormality_of_metabolism/homeostasis|Peroxisome_biogenesis_disorder_2B": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_5|Rhizomelic_chondrodysplasia_punctata": 1,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder": 1,
    "PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B|not_provided": 2,
    "Peroxisome_biogenesis_disorder_2B|not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Zellweger_spectrum_disorders|Peroxisome_biogenesis_disorder_2B": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B": 9,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Rhizomelic_chondrodysplasia_punctata_type_5": 4,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder_2B|not_specified": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_5|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|not_provided": 1,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 4,
    "Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_2B|not_provided|PEX5-related_disorder": 2,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|Rhizomelic_chondrodysplasia_punctata_type_5|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2B|Microcephaly": 1,
    "Inborn_genetic_diseases|PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_2B|not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|Microcephaly|PEX5-related_disorder|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder|Rhizomelic_chondrodysplasia_punctata_type_5|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_2B|Rhizomelic_chondrodysplasia_punctata_type_5|not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_1A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|not_provided|not_specified|Peroxisome_biogenesis_disorder_2B": 1,
    "not_provided|Peroxisome_biogenesis_disorder_2B|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|PEX5-related_disorder|Peroxisome_biogenesis_disorder_2B": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_2B": 1,
    "Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder|not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|not_specified": 1,
    "not_specified|Peroxisome_biogenesis_disorder_2B": 1,
    "Inborn_genetic_diseases|PEX5-related_disorder": 1,
    "not_provided|not_specified|Peroxisome_biogenesis_disorder_2B": 1,
    "not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Rhizomelic_chondrodysplasia_punctata_type_5|PEX5-related_disorder": 1,
    "Rhizomelic_chondrodysplasia_punctata_type_5": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|not_provided|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_2B|Peroxisome_biogenesis_disorder_2A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_2A_(Zellweger)|Peroxisome_biogenesis_disorder_2B|PEX5-related_disorder|Rhizomelic_chondrodysplasia_punctata_type_5": 1,
    "not_specified|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_2A_(Zellweger)": 2,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|not_provided": 2,
    "Microphthalmia|_isolated|_with_coloboma_6": 1,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|not_specified": 1,
    "not_specified|Klippel-Feil_syndrome_3|_autosomal_dominant|Isolated_microphthalmia_7": 1,
    "not_provided|Klippel-Feil_syndrome_3|_autosomal_dominant": 2,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|Isolated_microphthalmia_7|Microphthalmia|_isolated|_with_coloboma_6": 2,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|Isolated_microphthalmia_7|Microphthalmia|_isolated|_with_coloboma_6|not_specified": 1,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|Microphthalmia|_isolated|_with_coloboma_6|not_provided|GDF3-related_disorder|Supernumerary_ribs|Hemivertebrae|Scoliosis|Missing_ribs": 1,
    "Klippel-Feil_syndrome_3|_autosomal_dominant": 11,
    "GDF3-related_disorder": 2,
    "Microphthalmia|_isolated|_with_coloboma_6|Isolated_microphthalmia_7|not_provided": 1,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|Isolated_microphthalmia_7|Microphthalmia|_isolated|_with_coloboma_6|GDF3-related_disorder": 1,
    "GDF3-related_disorder|Klippel-Feil_syndrome_3|_autosomal_dominant|not_provided": 1,
    "Klippel-Feil_syndrome_3|_autosomal_dominant|not_provided|GDF3-related_disorder": 1,
    "C3AR1-related_disorder": 8,
    "not_specified|C3AR1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_21": 160,
    "Developmental_and_epileptic_encephalopathy|_21|not_provided|NECAP1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_21|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_21": 1,
    "not_specified|NECAP1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_21|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_21": 6,
    "NECAP1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_21|NECAP1-related_disorder": 1,
    "NECAP1-related_disorder|Developmental_and_epileptic_encephalopathy|_21|not_provided": 1,
    "NECAP1-related_disorder|Developmental_and_epileptic_encephalopathy|_21": 2,
    "not_provided|Hyper-IgM_syndrome_type_2": 10,
    "Hyper-IgM_syndrome_type_2": 204,
    "Hyper-IgM_syndrome_type_2|not_provided": 14,
    "Hyperimmunoglobulin_M_syndrome": 10,
    "Hyper-IgM_syndrome_type_2|not_provided|not_specified": 1,
    "not_provided|not_specified|Hyper-IgM_syndrome_type_2": 3,
    "Hyper-IgM_syndrome_type_2|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Hyper-IgM_syndrome_type_2|Hyperimmunoglobulin_M_syndrome|not_specified": 2,
    "Hyper-IgM_syndrome_type_2|not_provided|Hyperimmunoglobulin_M_syndrome": 1,
    "Hyper-IgM_syndrome_type_2|AICDA-related_disorder": 3,
    "AICDA-related_disorder|Hyper-IgM_syndrome_type_2": 2,
    "Inborn_genetic_diseases|Hyper-IgM_syndrome_type_2": 2,
    "Hyper-IgM_syndrome_type_2|Inborn_genetic_diseases": 4,
    "not_provided|Hyper-IgM_syndrome_type_2|AICDA-related_disorder": 1,
    "Hyper-IgM_syndrome_type_2|AICDA-related_disorder|not_specified": 1,
    "not_specified|not_provided|Hyper-IgM_syndrome_type_2": 1,
    "Isolated_thoracic_aortic_aneurysm|Aortic_aneurysm|_familial_thoracic_9|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|MFAP5-related_disorder": 2,
    "MFAP5-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_9|not_provided": 1,
    "not_provided|not_specified|MFAP5-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_9|not_specified|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_9|Cardiovascular_phenotype|not_provided": 1,
    "MFAP5-related_disorder|not_provided": 2,
    "not_provided|MFAP5-related_disorder": 1,
    "MFAP5-related_disorder|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|MFAP5-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_9": 1,
    "Aortic_aneurysm|_familial_thoracic_9": 1,
    "MFAP5-related_disorder|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_9|not_provided|not_specified": 1,
    "MFAP5-related_disorder": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_9": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_9|Cardiovascular_phenotype|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_9|not_provided": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_9": 2,
    "not_specified|Aortic_aneurysm|_familial_thoracic_9|not_provided": 1,
    "MFAP5-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Aortic_aneurysm|_familial_thoracic_9|not_provided": 1,
    "Otitis_media|_susceptibility_to|not_specified|not_provided": 5,
    "Otitis_media|_susceptibility_to|Otitis_media": 4,
    "not_specified|not_provided|A2ML1-related_disorder": 10,
    "not_specified|not_provided|Otitis_media|_susceptibility_to": 8,
    "not_provided|Otitis_media|Otitis_media|_susceptibility_to": 1,
    "not_provided|A2ML1-related_disorder|not_specified": 11,
    "not_provided|not_specified|A2ML1-related_disorder": 6,
    "A2ML1-related_disorder|not_provided|not_specified": 8,
    "not_provided|A2ML1-related_disorder": 6,
    "not_specified|A2ML1-related_disorder|not_provided": 5,
    "Otitis_media|_susceptibility_to": 3,
    "A2ML1-related_disorder|not_specified|not_provided": 12,
    "Nonsyndromic_otitis_media": 5,
    "Noonan_syndrome|not_provided|not_specified": 3,
    "Nonsyndromic_otitis_media|A2ML1-related_disorder|not_provided": 1,
    "Otitis_media|_susceptibility_to|not_provided|Otitis_media": 1,
    "A2ML1-related_disorder": 11,
    "Noonan_syndrome|not_specified|not_provided": 1,
    "A2ML1-related_disorder|not_provided": 4,
    "not_specified|A2ML1-related_disorder": 2,
    "A2ML1-related_disorder|not_specified": 1,
    "Otitis_media|_susceptibility_to|not_specified": 1,
    "A2ML1-related_disorder|Otitis_media|_susceptibility_to|not_specified|not_provided": 1,
    "Otitis_media|Otitis_media|_susceptibility_to|not_provided": 1,
    "Otitis_media|not_provided|not_specified|Otitis_media|_susceptibility_to|A2ML1-related_disorder": 1,
    "Otitis_media|Otitis_media|_susceptibility_to": 4,
    "not_provided|Otitis_media|_susceptibility_to|Otitis_media": 1,
    "A2ML1-related_disorder|not_specified|not_provided|Noonan_syndrome": 1,
    "Otitis_media|_susceptibility_to|A2ML1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Otitis_media|_susceptibility_to|Nonsyndromic_otitis_media": 1,
    "not_specified|Otitis_media|_susceptibility_to|not_provided": 1,
    "Nonsyndromic_otitis_media|not_provided|Otitis_media|_susceptibility_to|not_specified": 1,
    "Otitis_media|_susceptibility_to|Otitis_media|A2ML1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Otitis_media|_susceptibility_to|not_specified": 2,
    "not_provided|not_specified|Otitis_media|_susceptibility_to": 4,
    "not_provided|A2ML1-related_disorder|Nonsyndromic_otitis_media": 1,
    "Noonan_syndrome_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Otitis_media": 1,
    "Otitis_media|_susceptibility_to|not_provided|not_specified": 2,
    "not_specified|Noonan_syndrome|not_provided|A2ML1-related_disorder": 1,
    "Otitis_media|_susceptibility_to|not_specified|not_provided|Otitis_media": 1,
    "Microcephaly_11|_primary|_autosomal_recessive": 3,
    "not_provided|Microcephaly_11|_primary|_autosomal_recessive": 4,
    "PHC1-related_disorder": 4,
    "not_specified|not_provided|Microcephaly_11|_primary|_autosomal_recessive": 1,
    "PHC1-related_disorder|not_specified|not_provided": 1,
    "Microcephaly_11|_primary|_autosomal_recessive|not_specified": 1,
    "not_specified|PHC1-related_disorder": 1,
    "Primary_microcephaly|Intellectual_disability|Microcephaly_11|_primary|_autosomal_recessive": 1,
    "A2M-related_disorder": 16,
    "A2M-related_disorder|not_specified": 1,
    "not_provided|A2M-related_disorder": 1,
    "not_provided|ALPHA-2-MACROGLOBULIN_POLYMORPHISM": 1,
    "ALPHA-2-MACROGLOBULIN_POLYMORPHISM": 3,
    "not_specified|not_provided|ALPHA-2-MACROGLOBULIN_POLYMORPHISM": 1,
    "not_provided|Aspergillosis|_susceptibility_to": 1,
    "not_provided|CLEC7A-related_disorder": 1,
    "Aspergillosis|_susceptibility_to|CLEC7A-related_disorder|not_specified|not_provided|Familial_chronic_mucocutaneous_candidiasis": 1,
    "Aspergillosis|_susceptibility_to|Familial_chronic_mucocutaneous_candidiasis": 1,
    "Familial_chronic_mucocutaneous_candidiasis": 1,
    "CLEC7A-related_disorder": 2,
    "Familial_chronic_mucocutaneous_candidiasis|Aspergillosis|_susceptibility_to": 1,
    "not_provided|Familial_chronic_mucocutaneous_candidiasis|Aspergillosis|_susceptibility_to": 1,
    "not_provided|OLR1-related_disorder": 1,
    "OLR1-related_disorder": 2,
    "Myocardial_infarction|_susceptibility_to|OLR1-related_disorder": 1,
    "PRR4-related_disorder": 3,
    "PRB3M(NULL)": 1,
    "PRB3S(CYS)": 1,
    "ETV6-related_disorder": 7,
    "ETV6-related_disorder|not_provided": 3,
    "not_provided|ETV6-related_disorder": 2,
    "Thrombocytopenia_5|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|ETV6-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Thrombocytopenia_5|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Thrombocytopenia_5|not_specified": 1,
    "Thrombocytopenia_5": 14,
    "Thrombocytopenia_5|not_provided|ETV6-related_disorder|Inborn_genetic_diseases": 1,
    "ETV6-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "ETV6-related_disorder|Thrombocytopenia|Abnormal_bleeding": 1,
    "Thrombocytopenia_5|Inborn_genetic_diseases|not_specified|ETV6-related_disorder|not_provided": 1,
    "ETV6-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_5": 2,
    "Inborn_genetic_diseases|ETV6-related_disorder": 3,
    "not_provided|Thrombocytopenia_5|Acute_myeloid_leukemia|Inborn_genetic_diseases": 1,
    "ETV6-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ETV6-related_disorder|not_provided|Inborn_genetic_diseases|Thrombocytopenia_5": 1,
    "not_provided|ETV6-related_disorder|Inborn_genetic_diseases": 3,
    "Thrombocytopenia_5|not_provided|Inborn_genetic_diseases": 1,
    "Thrombocytopenia_5|Hematologic_neoplasm|Thrombocytopenia|Hereditary_cancer-predisposing_syndrome|not_provided|Acute_myeloid_leukemia": 1,
    "Thrombocytopenia_5|Inborn_genetic_diseases": 2,
    "Thrombocytopenia_5|ETV6-related_disorder": 1,
    "Thrombocytopenia_5|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|ETV6-related_disorder": 1,
    "Thrombocytopenia|Acute_lymphoid_leukemia|Inborn_genetic_diseases": 1,
    "not_provided|Thrombocytopenia_5|Inborn_genetic_diseases": 1,
    "not_provided|Thrombocytopenia_5|Thrombocytopenia": 1,
    "Inborn_genetic_diseases|ETV6-related_disorder|Thrombocytopenia_5|Hematologic_neoplasm|Thrombocytopenia|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|ETV6-related_disorder": 1,
    "ETV6-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Thrombocytopenia_5|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thrombocytopenia|See_cases|Acute_lymphoid_leukemia": 1,
    "Thrombocytopenia_5|Hematologic_neoplasm|Thrombocytopenia|not_provided": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_5|not_provided": 1,
    "Thrombocytopenia_5|Hermansky-Pudlak_syndrome_1": 1,
    "Inborn_genetic_diseases|Thrombocytopenia": 1,
    "not_provided|Thrombocytopenia_5": 1,
    "Inborn_genetic_diseases|ETV6-related_disorder|not_provided|Thrombocytopenia|Abnormal_bleeding": 1,
    "Orofacial_cleft|Tooth_agenesis": 3,
    "Coronary_artery_disease|_autosomal_dominant_2|Tooth_agenesis|_selective|_7|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|LRP6-related_disorder": 2,
    "Microcephaly|Short_stature|High_myopia|Sparse_scalp_hair|Generalized_hypopigmentation": 1,
    "Inborn_genetic_diseases|not_provided|LRP6-related_disorder|not_specified": 1,
    "Tooth_agenesis|_selective|_7": 14,
    "Tooth_agenesis|_selective|_7|Coronary_artery_disease|_autosomal_dominant_2": 3,
    "LRP6-related_disorder": 2,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Tooth_agenesis|_selective|_7": 1,
    "Tooth_agenesis|_selective|_7|Tooth_agenesis": 1,
    "LRP6-related_disorder|not_provided": 2,
    "Orofacial_cleft": 5,
    "not_provided|LRP6-related_disorder|Coronary_artery_disease|_autosomal_dominant_2|Tooth_agenesis|_selective|_7": 2,
    "not_provided|Coronary_artery_disease|_autosomal_dominant_2|Tooth_agenesis|_selective|_7": 1,
    "Oligodontia|Tooth_agenesis|_selective|_7|Coronary_artery_disease|_autosomal_dominant_2": 1,
    "not_provided|Coronary_artery_disease|_autosomal_dominant_2": 1,
    "Tooth_agenesis|_selective|_7|not_provided": 2,
    "not_provided|LRP6-related_disorder|Inborn_genetic_diseases": 1,
    "LRP6-related_disorder|Coronary_artery_disease|_autosomal_dominant_2": 1,
    "Tooth_agenesis|_selective|_7|Coronary_artery_disease|_autosomal_dominant_2|Hypodontia|not_provided": 1,
    "Coronary_artery_disease|_autosomal_dominant_2|not_provided": 3,
    "Tooth_agenesis|not_provided|Tooth_agenesis|_selective|_7": 1,
    "Coronary_artery_disease|_autosomal_dominant_2|Tooth_agenesis|_selective|_7": 2,
    "Inborn_genetic_diseases|not_provided|Tooth_agenesis|_selective|_7": 1,
    "Coronary_artery_disease|_autosomal_dominant_2|Tooth_agenesis|_selective|_7|not_provided|LRP6-related_disorder|Inborn_genetic_diseases": 1,
    "LRP6-related_disorder|not_provided|not_specified": 1,
    "LRP6-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Tooth_agenesis|_selective|_7": 1,
    "not_provided|Corpus_callosum|_agenesis_of|Global_developmental_delay|Polymicrogyria|Seizure|Abnormal_cerebral_cortex_morphology|Microcephaly": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_4": 5,
    "Multiple_endocrine_neoplasia_type_4": 300,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 190,
    "Multiple_endocrine_neoplasia": 4,
    "Multiple_endocrine_neoplasia_type_4|not_provided": 6,
    "not_provided|Primary_hyperparathyroidism|Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder": 1,
    "CDKN1B-related_disorder|Multiple_endocrine_neoplasia|not_specified|not_provided|Primary_hyperparathyroidism|Multiple_endocrine_neoplasia_type_4": 1,
    "not_provided|CDKN1B-related_disorder": 1,
    "CDKN1B-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_4": 17,
    "Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome": 181,
    "CDKN1B-related_disorder|not_provided|Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome|not_provided": 18,
    "Multiple_endocrine_neoplasia_type_4|not_provided|Hereditary_cancer-predisposing_syndrome": 12,
    "not_provided|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 1,
    "not_provided|Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome": 17,
    "CDKN1B-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 2,
    "CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 10,
    "CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia_type_4": 2,
    "Neuroendocrine_neoplasm": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 1,
    "Multiple_endocrine_neoplasia_type_4|not_provided|CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|CDKN1B-related_disorder|Multiple_endocrine_neoplasia_type_4": 2,
    "Multiple_endocrine_neoplasia|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia_type_4": 1,
    "Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 1,
    "Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4|not_provided|CDKN1B-related_disorder": 1,
    "Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome|CDKN1B-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4|not_provided": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4|Colorectal_cancer": 1,
    "Multiple_endocrine_neoplasia_type_4|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Neuroendocrine_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "CDKN1B-related_disorder|Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|Multiple_endocrine_neoplasia_type_4|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4": 3,
    "not_specified|Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4|Ovarian_cancer": 1,
    "Ovarian_cancer|Multiple_endocrine_neoplasia_type_4": 1,
    "Primary_hyperparathyroidism|Hereditary_cancer-predisposing_syndrome|CDKN1B-related_disorder|not_specified|Multiple_endocrine_neoplasia_type_4|not_provided": 1,
    "Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|not_specified|Multiple_endocrine_neoplasia_type_4": 1,
    "Multiple_endocrine_neoplasia_type_4|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder": 1,
    "Multiple_endocrine_neoplasia_type_4|CDKN1B-related_disorder": 1,
    "CDKN1B-related_disorder|Multiple_endocrine_neoplasia_type_4|Multiple_endocrine_neoplasia|Hereditary_cancer-predisposing_syndrome": 1,
    "CDKN1B-related_disorder|Multiple_endocrine_neoplasia_type_4|Hereditary_cancer-predisposing_syndrome": 2,
    "CDKN1B-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Multiple_endocrine_neoplasia_type_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Multiple_endocrine_neoplasia_type_4|Hereditary_nonpolyposis_colon_cancer|not_provided": 1,
    "Bleeding_disorder|_vascular-type": 1,
    "FAM234B-related_disorder": 12,
    "FAM234B-related_disorder|not_provided": 1,
    "not_provided|Intellectual_Disability|_Dominant": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 370,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 397,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided": 41,
    "not_specified|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 10,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 5,
    "Developmental_and_epileptic_encephalopathy|_27": 29,
    "not_provided|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 28,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|Inborn_genetic_diseases": 14,
    "not_specified|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 11,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 5,
    "Inborn_genetic_diseases|Landau-Kleffner_syndrome|Intellectual_disability|_autosomal_dominant_6": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|not_specified": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 42,
    "GRIN2B-related_disorder": 8,
    "Intellectual_disability|_autosomal_dominant_6": 94,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases": 16,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided": 31,
    "not_provided|GRIN2B-related_developmental_delay|_intellectual_disability_and_autism_spectrum_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided": 2,
    "GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified": 18,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 14,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 4,
    "not_specified|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|Inborn_genetic_diseases|not_specified": 1,
    "GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 2,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|GRIN2B-related_disorder|not_provided": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 3,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 2,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified|not_provided": 2,
    "not_specified|GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 8,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|Inborn_genetic_diseases": 5,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 4,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided|not_specified": 1,
    "GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided": 2,
    "not_specified|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|GRIN2B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|Inborn_genetic_diseases": 5,
    "GRIN2B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Paroxysmal_dystonia": 1,
    "Inborn_genetic_diseases|GRIN2B-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "not_provided|GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified": 4,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified|not_provided": 3,
    "GRIN2B-related_disorder|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified": 2,
    "not_provided|not_specified|GRIN2B-related_disorder|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 1,
    "Developmental_and_epileptic_encephalopathy|_27|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|GRIN2B-related_disorder": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6": 7,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|developmental_delay_with_intractable_seizures|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided|Inborn_genetic_diseases|GRIN2B-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_6|not_provided": 6,
    "not_provided|Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|GRIN2B-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_6|GRIN2B-related_disorder|Intellectual_disability|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified|not_provided": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 1,
    "Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_6|not_provided": 1,
    "GRIN2B-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_6": 1,
    "not_provided|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "GRIN2B-related_disorder|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_27|not_provided|Intellectual_disability|_autosomal_dominant_6": 2,
    "Lennox-Gastaut_syndrome|GRIN2B-related_developmental_delay|_intellectual_disability_and_autism_spectrum_disorder|West_syndrome|Intellectual_disability|_autosomal_dominant_6": 1,
    "Intellectual_disability|Developmental_delay": 2,
    "Intellectual_disability|Complex_neurodevelopmental_disorder|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Intellectual_disability|Atypical_behavior|Autistic_behavior|Seizure": 1,
    "Intellectual_disability|_severe|Craniosynostosis_syndrome|Seizure|Fetal_growth_restriction|Atypical_behavior|Abnormal_facial_shape|Self-injurious_behavior|Scoliosis|Absent_speech|Microcephaly|Difficulty_walking": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|GRIN2B-related_disorder|not_specified": 1,
    "intellectual_deficiency|Ataxia|Epilepsy|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|Complex_neurodevelopmental_disorder|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Ataxia|intellectual_deficiency": 1,
    "Intellectual_disability|_autosomal_dominant_6|GRIN2B-related_disorder|Complex_neurodevelopmental_disorder": 1,
    "Developmental_disorder|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_27|not_provided|Intellectual_disability|_autosomal_dominant_6|Intellectual_disability": 1,
    "Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_6": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified": 5,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Astigmatism|Long_fingers|Joint_hypermobility|Delayed_speech_and_language_development|Motor_delay|not_provided|Intellectual_disability": 1,
    "GRIN2B-related_disorder|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 2,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_27|not_specified|not_provided": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_6": 1,
    "Developmental_and_epileptic_encephalopathy|_27|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_27": 1,
    "GRIN2B-related_developmental_delay|_intellectual_disability_and_autism_spectrum_disorder": 2,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 2,
    "not_specified|GRIN2B-related_disorder|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 1,
    "GRIN2B-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Cerebral_palsy": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified|Inborn_genetic_diseases": 1,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified|not_provided|intellectual_deficiency|See_cases": 1,
    "Intellectual_disability|_autosomal_dominant_6|not_specified|Developmental_and_epileptic_encephalopathy|_27|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_6|Complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|Inborn_genetic_diseases|GRIN2B-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided|not_specified|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|GRIN2B-related_disorder": 1,
    "not_provided|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|Intellectual_disability|_autosomal_dominant_6": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Sleep_abnormality|Self-injurious_behavior|Intellectual_disability|_autosomal_dominant_6|Hypotonia|Atypical_behavior|Intellectual_disability|Microcephaly": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|See_cases": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_dominant_non-syndromic_intellectual_disability|not_provided|Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_6": 1,
    "Intellectual_disability|_autosomal_dominant_6|Neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|See_cases": 1,
    "Inborn_genetic_diseases|GRIN2B-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_specified|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases|GRIN2B-related_disorder": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|Inborn_genetic_diseases|not_provided": 1,
    "GRIN2B-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|not_provided|Intellectual_disability|_autosomal_dominant_6|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|GRIN2B-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 1,
    "GRIN2B-related_disorder|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided": 1,
    "not_specified|GRIN2B-related_disorder": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_6|not_provided": 1,
    "GRIN2B-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Developmental_and_epileptic_encephalopathy|_27|Intellectual_disability|_autosomal_dominant_6|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27": 1,
    "Intellectual_disability|_autosomal_dominant_6|Developmental_and_epileptic_encephalopathy|_27|Inborn_genetic_diseases|not_specified": 1,
    "Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|not_provided": 4,
    "not_provided|GUCY2C-related_disorder": 5,
    "Congenital_diarrhea_6": 9,
    "Congenital_diarrhea_6|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|not_provided": 3,
    "Meconium_ileus": 4,
    "GUCY2C-related_disorder": 9,
    "not_specified|not_provided|GUCY2C-related_disorder": 1,
    "not_provided|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|Congenital_diarrhea_6|Inborn_genetic_diseases": 1,
    "Congenital_diarrhea_6|not_provided": 1,
    "GUCY2C-related_disorder|not_provided": 7,
    "Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|not_provided|not_specified|Congenital_diarrhea_6": 1,
    "Meconium_ileus|not_provided": 1,
    "Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|Congenital_diarrhea_6|not_specified|not_provided": 1,
    "not_provided|Meconium_ileus|not_specified": 1,
    "Congenital_diarrhea_6|Meconium_ileus|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|not_provided": 1,
    "Congenital_diarrhea_6|Inborn_genetic_diseases|not_provided": 1,
    "Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency": 1,
    "Congenital_diarrhea_6|Meconium_ileus|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_diarrhea_6|Meconium_ileus|not_provided": 1,
    "Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|Congenital_diarrhea_6|not_provided": 1,
    "not_provided|Meconium_ileus": 2,
    "not_provided|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency": 2,
    "not_provided|Congenital_diarrhea_6|Meconium_ileus": 1,
    "Congenital_diarrhea_6|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency": 1,
    "not_provided|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|Congenital_diarrhea_6": 1,
    "Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency|Congenital_diarrhea_6|not_provided|not_specified": 1,
    "not_provided|Congenital_diarrhea_6|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency": 2,
    "Abnormal_biliary_tract_morphology|Asplenia|Duodenal_atresia|Reduced_number_of_intrahepatic_bile_ducts": 1,
    "GUCY2C-related_disorder|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Intestinal_obstruction_in_the_newborn_due_to_guanylate_cyclase_2C_deficiency": 1,
    "not_provided|Vertebral|_cardiac|_tracheoesophageal|_renal|_and_limb_defects": 2,
    "Vertebral|_cardiac|_tracheoesophageal|_renal|_and_limb_defects|WBP11_spliceosomopathy": 4,
    "Vertebral|_cardiac|_tracheoesophageal|_renal|_and_limb_defects": 12,
    "WBP11-related_disorder": 2,
    "Inborn_genetic_diseases|Vertebral|_cardiac|_tracheoesophageal|_renal|_and_limb_defects": 1,
    "WBP11_spliceosomopathy": 2,
    "ART4-related_disorder": 3,
    "ART4-related_disorder|Blood_group|_Dombrock_system": 1,
    "Blood_group|_Dombrock_system": 4,
    "Keutel_syndrome": 22,
    "not_provided|Keutel_syndrome": 9,
    "Keutel_syndrome|not_provided": 1,
    "not_provided|not_specified|Keutel_syndrome": 1,
    "not_provided|MGP-related_disorder": 2,
    "MGP-related_disorder|not_provided": 1,
    "MGP-related_disorder|not_provided|Keutel_syndrome": 1,
    "Keutel_syndrome|not_specified|not_provided": 1,
    "not_specified|Keutel_syndrome|not_provided|MGP-related_disorder": 1,
    "not_provided|MGP-related_disorder|Keutel_syndrome": 1,
    "MGP-related_disorder": 2,
    "Short_stature|Platyspondyly|Short_palm|Short_distal_phalanx_of_finger|Spondyloepiphyseal_dysplasia|not_provided": 1,
    "not_specified|Keutel_syndrome|MGP-related_disorder|not_provided": 1,
    "Retinal_cone_dystrophy_3A": 9,
    "not_provided|Retinal_cone_dystrophy_3A": 7,
    "PDE6H-related_disorder|Retinal_cone_dystrophy_3A|Retinal_dystrophy|not_provided": 1,
    "Retinal_cone_dystrophy_3A|not_provided": 1,
    "Nephrotic_syndrome|_type_6": 114,
    "not_provided|PTPRO-related_disorder": 7,
    "PTPRO-related_disorder|Nephrotic_syndrome|_type_6|not_provided": 1,
    "PTPRO-related_disorder": 16,
    "Nephrotic_syndrome|_type_6|not_specified": 11,
    "not_provided|Nephrotic_syndrome|_type_6": 10,
    "Nephrotic_syndrome|_type_6|not_specified|not_provided": 1,
    "Nephrotic_syndrome|_type_6|not_provided": 8,
    "not_specified|not_provided|Nephrotic_syndrome|_type_6": 2,
    "not_provided|not_specified|Corticosteroids_response": 1,
    "not_specified|Nephrotic_syndrome|_type_6|not_provided": 2,
    "PTPRO-related_disorder|not_provided|not_specified|Nephrotic_syndrome|_type_6": 1,
    "not_specified|Nephrotic_syndrome|_type_6": 3,
    "Nephrotic_syndrome|_type_6|PTPRO-related_disorder|not_provided": 1,
    "PTPRO-related_disorder|not_provided": 4,
    "Nephrotic_syndrome|_type_6|not_provided|PTPRO-related_disorder": 1,
    "not_provided|Nephrotic_syndrome|_type_6|PTPRO-related_disorder": 1,
    "Corticosteroids_response|Nephrotic_syndrome|_type_6|not_provided": 1,
    "Nephrotic_syndrome|_type_6|PTPRO-related_disorder": 1,
    "not_provided|EPS8-related_disorder": 8,
    "not_specified|not_provided|EPS8-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_102|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_102|not_provided|Inborn_genetic_diseases": 1,
    "EPS8-related_disorder|not_provided": 6,
    "Inborn_genetic_diseases|EPS8-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_102": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_102": 1,
    "not_specified|EPS8-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_102": 9,
    "not_specified|not_provided|Inborn_genetic_diseases|Deafness": 1,
    "EPS8-related_disorder": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_102|EPS8-related_disorder": 1,
    "not_provided|not_specified|EPS8-related_disorder": 1,
    "EPS8-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_102|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_102|Deafness|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_102|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hearing_loss|_autosomal_recessive_106|Autosomal_recessive_nonsyndromic_hearing_loss_102|not_provided": 1,
    "PLCZ1-related_disorder": 2,
    "Spermatogenic_failure_17|PLCZ1-related_disorder": 1,
    "Spermatogenic_failure_17": 11,
    "not_provided|PLCZ1-related_disorder": 1,
    "PLEKHA5-related_disorder": 19,
    "PLEKHA5-related_disorder|not_provided": 1,
    "not_provided|PLEKHA5-related_disorder": 2,
    "Bilateral_cleft_lip": 1,
    "PLEKHA5-related_disorder|not_specified": 2,
    "PDE3A-related_disorder": 7,
    "not_provided|PDE3A-related_disorder": 7,
    "Brachydactyly-arterial_hypertension_syndrome": 16,
    "not_provided|Inborn_genetic_diseases|PDE3A-related_disorder": 1,
    "PDE3A-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Brachydactyly-arterial_hypertension_syndrome": 2,
    "not_provided|Brachydactyly-arterial_hypertension_syndrome": 1,
    "Brachydactyly-arterial_hypertension_syndrome|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|Brachydactyly-arterial_hypertension_syndrome": 1,
    "PDE3A-related_disorder|not_provided|Brachydactyly-arterial_hypertension_syndrome": 1,
    "Brachydactyly-arterial_hypertension_syndrome|Inborn_genetic_diseases": 1,
    "PDE3A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Rotor_syndrome": 14,
    "Rotor_syndrome": 176,
    "Rotor_syndrome|not_provided": 18,
    "Rotor_syndrome|not_specified": 4,
    "Rotor_syndrome|not_provided|SLCO1B3-related_disorder": 4,
    "SLCO1B3-related_disorder": 44,
    "not_specified|Rotor_syndrome": 4,
    "Rotor_syndrome|SLCO1B3-related_disorder|not_provided": 2,
    "Rotor_syndrome|SLCO1B3-related_disorder": 13,
    "SLCO1B3-related_disorder|Rotor_syndrome": 7,
    "not_provided|Rotor_syndrome|SLCO1B3-related_disorder": 3,
    "not_specified|Rotor_syndrome|not_provided": 1,
    "not_provided|SLCO1B3-related_disorder|Rotor_syndrome": 2,
    "SLCO1B3-related_disorder|not_specified": 1,
    "not_provided|not_specified|Rotor_syndrome": 2,
    "not_provided|SLCO1B3-related_disorder": 1,
    "Rotor_syndrome|not_provided|not_specified": 1,
    "not_provided|Rotor_syndrome|Gilbert_syndrome|not_specified": 1,
    "Rotor_syndrome|SLCO1B1-related_disorder|not_provided": 3,
    "Rotor_syndrome|SLCO1B1-related_disorder|not_specified|not_provided": 1,
    "Rotor_syndrome|SLCO1B1-related_disorder": 1,
    "SLCO1B1-related_disorder|not_specified|not_provided|Rotor_syndrome|Gilbert_syndrome|simvastatin_acid_response_-_Metabolism/PK|lovastatin_response_-_Toxicity|pitavastatin_response_-_Metabolism/PK|pravastatin_response_-_Toxicity|rosuvastatin_response_-_Toxicity|simvastatin_response_-_Metabolism/PK|fluvastatin_response_-_Metabolism/PK|fluvastatin_response_-_Toxicity|lovastatin_acid_response_-_Metabolism/PK|lovastatin_response_-_Metabolism/PK|rosuvastatin_response_-_Metabolism/PK|atorvastatin_response_-_Metabolism/PK|atorvastatin_response_-_Toxicity|hmg_coa_reductase_inhibitors_response_-_Toxicity|simvastatin_response_-_Toxicity": 1,
    "not_specified|not_provided|SLCO1B1-related_disorder|Rotor_syndrome": 1,
    "SLCO1B1-related_disorder|Rotor_syndrome|not_provided|not_specified": 1,
    "Rotor_syndrome|not_specified|not_provided": 1,
    "not_provided|SLCO1B1-related_disorder": 1,
    "not_provided|SLCO1B1-related_disorder|Rotor_syndrome": 1,
    "Cardiovascular_phenotype|Rotor_syndrome": 2,
    "SLCO1B1-related_disorder": 2,
    "Rotor_syndrome|Cardiovascular_phenotype": 2,
    "SLCO1B1-related_disorder|not_provided|Rotor_syndrome": 2,
    "not_specified|not_provided|Rotor_syndrome": 1,
    "Rotor_syndrome|See_cases": 1,
    "not_provided|Myofibrillar_myopathy_8": 9,
    "Myofibrillar_myopathy_8": 8,
    "Myofibrillar_myopathy_8|not_provided": 7,
    "Inborn_genetic_diseases|Myofibrillar_myopathy_8|not_provided": 1,
    "not_provided|PYROXD1-related_disorder": 4,
    "PYROXD1-related_disorder|not_provided": 2,
    "RECON_progeroid_syndrome|not_provided": 5,
    "RECQL-related_disorder|not_specified": 2,
    "RECON_progeroid_syndrome": 5,
    "not_provided|RECON_progeroid_syndrome|not_specified": 4,
    "RECON_progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|RECON_progeroid_syndrome": 5,
    "Familial_ovarian_cancer|not_provided": 1,
    "not_provided|not_specified|RECON_progeroid_syndrome": 4,
    "not_specified|RECON_progeroid_syndrome": 2,
    "RECON_progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|RECON_progeroid_syndrome|not_provided": 3,
    "not_specified|RECQL-related_disorder|not_provided": 2,
    "not_specified|not_provided|RECON_progeroid_syndrome": 6,
    "RECON_progeroid_syndrome|not_specified": 3,
    "RECQL-related_disorder|not_specified|not_provided": 3,
    "not_provided|RECQL-related_disorder|not_specified": 2,
    "RECQL-related_disorder|not_provided": 1,
    "not_specified|RECQL-related_disorder|RECON_progeroid_syndrome|not_provided": 1,
    "RECON_progeroid_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|RECQL-related_disorder": 1,
    "Hereditary_cancer|not_specified|not_provided|RECON_progeroid_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 18,
    "not_specified|RECON_progeroid_syndrome|Short_stature|Abnormal_facial_shape": 1,
    "not_provided|Familial_ovarian_cancer": 1,
    "RECQL-related_disorder|not_provided|not_specified": 3,
    "not_specified|RECQL-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|RECON_progeroid_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|RECQL-related_disorder|RECON_progeroid_syndrome|Familial_ovarian_cancer": 1,
    "not_provided|RECQL-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "RECON_progeroid_syndrome|not_provided|not_specified|RECQL-related_disorder": 1,
    "not_provided|RECQL-related_disorder": 3,
    "not_specified|not_provided|RECQL-related_disorder": 2,
    "RECON_progeroid_syndrome|not_specified|not_provided": 4,
    "Familial_cancer_of_breast|not_provided|not_specified": 1,
    "RECQL-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer": 3,
    "RECON_progeroid_syndrome|Hereditary_cancer|not_specified|not_provided": 1,
    "RECQL-related_disorder|RECON_progeroid_syndrome|not_specified|not_provided|Hereditary_cancer": 1,
    "Seizure|RECQL-related_disorder|Hereditary_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "RECQL-related_disorder": 1,
    "not_specified|not_provided|Hereditary_cancer": 1,
    "RECON_progeroid_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "RECON_progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|RECQL-related_disorder|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|RECON_progeroid_syndrome|not_specified|RECQL-related_disorder|not_provided": 1,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 133,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_provided": 8,
    "not_specified|not_provided|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 6,
    "Inborn_genetic_diseases|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 9,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_provided|not_specified": 4,
    "not_specified|not_provided|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|GYS2-related_disorder": 1,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|Inborn_genetic_diseases": 6,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_specified|not_provided": 2,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_specified": 9,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|GYS2-related_disorder": 1,
    "not_provided|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 6,
    "GYS2-related_disorder": 6,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "GYS2-related_disorder|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 7,
    "not_specified|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 3,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|GYS2-related_disorder|not_specified": 1,
    "not_provided|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_specified": 3,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_provided|not_specified|GYS2-related_disorder": 1,
    "not_specified|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_provided": 4,
    "GYS2-related_disorder|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Glycogen_storage_disease": 1,
    "GYS2-related_disorder|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_specified": 1,
    "not_provided|not_specified|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency": 1,
    "GYS2-related_disorder|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_specified|GYS2-related_disorder": 1,
    "Glycogen_storage_disease|Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|not_provided|GYS2-related_disorder|See_cases": 1,
    "Glycogen_storage_disorder_due_to_hepatic_glycogen_synthase_deficiency|See_cases": 1,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_H-subunit_deficiency": 26,
    "Glycogen_storage_disease_due_to_lactate_dehydrogenase_H-subunit_deficiency|not_provided": 3,
    "not_specified|Glycogen_storage_disease_due_to_lactate_dehydrogenase_H-subunit_deficiency": 2,
    "LDHB-related_disorder|Glycogen_storage_disease_due_to_lactate_dehydrogenase_H-subunit_deficiency": 2,
    "not_provided|LDHB-related_disorder": 1,
    "not_provided|Glycogen_storage_disease_due_to_lactate_dehydrogenase_H-subunit_deficiency": 1,
    "KCNJ8-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Brugada_syndrome": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|Sudden_unexplained_death": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|SUDDEN_INFANT_DEATH_SYNDROME|Brugada_syndrome": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type": 17,
    "Brugada_syndrome|KCNJ8-related_disorder|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|KCNJ8-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|Brugada_syndrome_1": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|KCNJ8-related_disorder|not_provided|Cardiovascular_phenotype|Brugada_syndrome": 1,
    "Brugada_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Brugada_syndrome|not_provided|Syndromic_disease|KCNJ8-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiac_arrest|Brugada_syndrome": 1,
    "not_provided|ABCC9-related_disorder": 1,
    "ABCC9-related_disorder|not_specified": 1,
    "Dilated_cardiomyopathy_1O": 923,
    "Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O": 1,
    "Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome": 1,
    "Dilated_cardiomyopathy_1O|Hypertrophic_cardiomyopathy|Cardiomyopathy|Atrial_fibrillation|_familial|_12": 1,
    "Dilated_cardiomyopathy_1O|not_provided": 29,
    "Dilated_cardiomyopathy_1O|not_specified|not_provided": 4,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 93,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_provided|ABCC9-related_disorder": 1,
    "not_provided|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O|not_provided|Cardiomyopathy|Intellectual_disability": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "not_provided|Dilated_cardiomyopathy_1O": 23,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 84,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 14,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1O": 2,
    "not_provided|not_specified|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 1,
    "ABCC9-related_disorder": 8,
    "not_provided|Dilated_cardiomyopathy_1O|not_specified": 6,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1O": 3,
    "not_specified|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 6,
    "not_provided|Dilated_cardiomyopathy_1O|not_specified|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_2|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1O|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1O|not_specified": 22,
    "not_specified|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_specified": 5,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type": 5,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_Cardiomyopathy|_Dominant|Familial_atrial_fibrillation": 3,
    "not_specified|Dilated_cardiomyopathy_1O": 20,
    "Intellectual_disability_and_myopathy_syndrome": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type": 2,
    "Dilated_cardiomyopathy_1O|not_specified|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|not_provided": 1,
    "Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome": 2,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "Dilated_cardiomyopathy_1O|not_specified|Cardiovascular_phenotype": 5,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Cardiomyopathy": 1,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1O": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Cardiomyopathy|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Dilated_cardiomyopathy_1O": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|not_provided|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_specified|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|not_provided": 2,
    "Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 5,
    "Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|not_provided|Cardiovascular_phenotype": 1,
    "ABCC9-related_disorder|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Epicanthus|Patent_ductus_arteriosus|Tapered_finger|Micrognathia|Thick_upper_lip_vermilion|Depressed_nasal_bridge|Bulbous_nose|Coarse_facial_features|Macrocephaly|Abnormality_of_the_face|Low_anterior_hairline|Left_ventricular_hypertrophy|Large_hands|Abnormal_facial_shape|Joint_hypermobility|ABCC9-related_disorder|Dilated_cardiomyopathy_1O|not_provided": 1,
    "Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1O|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Kleefstra_syndrome_1|not_provided|Cardiovascular_phenotype": 1,
    "ABCC9-related_disorder|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1O|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "not_specified|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided": 1,
    "ABCC9-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1O": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_provided|ABCC9-related_disorder": 1,
    "Dilated_cardiomyopathy_1O|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "not_provided|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 9,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1O": 7,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 2,
    "not_provided|Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|ABCC9-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|ABCC9-related_disorder|Dilated_cardiomyopathy_1O|not_specified|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1O|ABCC9-related_disorder|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_specified": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Atrial_fibrillation|_familial|_12": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1O|not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12": 1,
    "Dilated_cardiomyopathy_1O|Cardiomyopathy": 4,
    "not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|ABCC9-related_disorder": 1,
    "Dilated_cardiomyopathy_1O|ABCC9-related_disorder|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1O|not_provided|not_specified": 4,
    "not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1O|Primary_dilated_cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Intellectual_disability_and_myopathy_syndrome|Dilated_cardiomyopathy_1O": 2,
    "not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Dilated_cardiomyopathy_1O|not_provided": 2,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_provided": 6,
    "not_specified|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided": 1,
    "ABCC9-related_disorder|Dilated_cardiomyopathy_1O": 1,
    "Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|not_specified": 1,
    "Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|not_provided|Cardiovascular_phenotype": 1,
    "ABCC9-related_disorder|not_specified|Dilated_cardiomyopathy_1O|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "ABCC9-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_2|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Familial_atrial_fibrillation|not_specified|not_provided": 1,
    "not_provided|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Ventricular_tachycardia|not_specified|not_provided|Dilated_cardiomyopathy_1O|Myocardial_infarction": 1,
    "Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_specified": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1O": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Primary_familial_dilated_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 3,
    "Dilated_cardiomyopathy_1O|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_specified": 3,
    "ABCC9-related_disorder|not_specified|not_provided|Brugada_syndrome|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12": 1,
    "not_provided|Dilated_cardiomyopathy_1O|not_specified|Cardiovascular_phenotype|ABCC9-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1A|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12": 1,
    "Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome": 2,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Conduction_disorder_of_the_heart|Dilated_cardiomyopathy_1O|not_provided|not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiomyopathy": 1,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Primary_familial_dilated_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|ABCC9-related_disorder|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|not_provided": 1,
    "Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|not_provided|ABCC9-related_disorder": 1,
    "Dilated_cardiomyopathy_1O|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|ABCC9-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Cardiomyopathy|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|not_provided": 1,
    "not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|not_specified": 2,
    "not_provided|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_provided|ABCC9-related_disorder|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiomyopathy": 1,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 1,
    "not_specified|Dilated_cardiomyopathy_1O|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided|Dilated_cardiomyopathy_1O": 1,
    "Cardiovascular_phenotype|ABCC9-related_disorder|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 3,
    "Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Intellectual_disability_and_myopathy_syndrome|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|ABCC9-related_disorder|not_specified|not_provided": 1,
    "Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|not_provided|Dilated_cardiomyopathy_1O|Familial_atrial_fibrillation|not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Dilated_Cardiomyopathy|_Dominant|Dilated_cardiomyopathy_1O|not_provided|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type|Hypertrophic_cardiomyopathy_2|not_specified": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_Cardiomyopathy|_Dominant|Familial_atrial_fibrillation|not_specified|not_provided": 1,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_specified": 2,
    "not_provided|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_specified": 1,
    "Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1O|not_provided": 1,
    "not_provided|not_specified|ABCC9-related_disorder|Dilated_cardiomyopathy_1O": 1,
    "Dilated_cardiomyopathy_1O|not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|not_specified|not_provided": 1,
    "ABCC9-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O|not_provided": 1,
    "Dilated_cardiomyopathy_1O|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "not_provided|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiomyopathy|Dilated_cardiomyopathy_1O": 1,
    "Dilated_cardiomyopathy_1O|not_specified|Cardiomyopathy|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1O|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_2|Dilated_cardiomyopathy_1O|not_specified": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1O": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1O|not_provided|not_specified": 1,
    "ABCC9-related_disorder|not_specified|not_provided|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Intellectual_disability_and_myopathy_syndrome": 1,
    "Dilated_cardiomyopathy_1O|not_specified|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_specified|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided": 1,
    "Dilated_cardiomyopathy_1O|ABCC9-related_disorder": 1,
    "not_specified|not_provided|Dilated_cardiomyopathy_1O": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_specified": 1,
    "Hypertrichotic_osteochondrodysplasia_Cantu_type|not_provided": 1,
    "Dilated_cardiomyopathy_1O|not_specified|Intellectual_disability_and_myopathy_syndrome|Hypertrichotic_osteochondrodysplasia_Cantu_type|Atrial_fibrillation|_familial|_12|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrichotic_osteochondrodysplasia_Cantu_type|Dilated_cardiomyopathy_1O": 1,
    "ABCC9-related_disorder|not_specified|Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1O|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type|Intellectual_disability_and_myopathy_syndrome": 1,
    "not_specified|Dilated_cardiomyopathy_1O|Hypertrichotic_osteochondrodysplasia_Cantu_type|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1O": 1,
    "Dilated_cardiomyopathy_1O|Cardiovascular_phenotype|Hypertrichotic_osteochondrodysplasia_Cantu_type|not_specified": 1,
    "Dilated_cardiomyopathy_1O|Intellectual_disability_and_myopathy_syndrome|Atrial_fibrillation|_familial|_12|Hypertrichotic_osteochondrodysplasia_Cantu_type": 1,
    "Lamb-Shaffer_syndrome": 67,
    "SOX5-related_disorder|Inborn_genetic_diseases": 1,
    "Lamb-Shaffer_syndrome|Intellectual_disability": 1,
    "Lamb-Shaffer_syndrome|not_provided": 12,
    "SOX5-related_disorder": 9,
    "Intellectual_disability|Lamb-Shaffer_syndrome": 1,
    "Lamb-Shaffer_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Lamb-Shaffer_syndrome|Neurodevelopmental_delay|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Lamb-Shaffer_syndrome": 2,
    "Inborn_genetic_diseases|Lamb-Shaffer_syndrome": 5,
    "Inborn_genetic_diseases|Lamb-Shaffer_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|SOX5-related_disorder": 2,
    "Lamb-Shaffer_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Lamb-Shaffer_syndrome|Inborn_genetic_diseases": 2,
    "SOX5-related_disorder|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Lamb-Shaffer_syndrome": 1,
    "Severe_global_developmental_delay|Generalized_hypotonia|Epileptic_encephalopathy": 1,
    "Lamb-Shaffer_syndrome|Aplasia/Hypoplasia_of_the_nails|Generalized_hypotonia|Central_hypotonia|Thoracolumbar_scoliosis|Strabismus": 1,
    "See_cases|Lamb-Shaffer_syndrome": 1,
    "Lamb-Shaffer_syndrome|not_specified": 1,
    "BCAT1-related_disorder": 6,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome|not_provided": 2,
    "Noonan_syndrome|Cardio-facio-cutaneous_syndrome|not_provided": 3,
    "Cardio-facio-cutaneous_syndrome|Noonan_syndrome": 7,
    "Noonan_syndrome|Cardio-facio-cutaneous_syndrome": 8,
    "RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome": 1,
    "Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 3,
    "not_provided|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "not_provided|RASopathy|Noonan_syndrome_3|Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Familial_pancreatic_carcinoma|Gastric_cancer|Lung_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Noonan_syndrome": 1,
    "Toriello-Lacassie-Droste_syndrome": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|KRAS-related_disorder|not_provided|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_3|RASopathy": 2,
    "Familial_cancer_of_breast|Noonan_syndrome_3|Malignant_tumor_of_urinary_bladder|Acute_myeloid_leukemia|Lung_cancer|Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Cardiofaciocutaneous_syndrome_2|Familial_pancreatic_carcinoma|RASopathy": 1,
    "RASopathy|not_provided|KRAS-related_disorder|Cardiofaciocutaneous_syndrome_2": 1,
    "Noonan_syndrome_3|Noonan_syndrome|Cardio-facio-cutaneous_syndrome|not_provided": 1,
    "Acute_myeloid_leukemia|Linear_nevus_sebaceous_syndrome|Lung_carcinoma|Autoimmune_lymphoproliferative_syndrome_type_4|Malignant_tumor_of_urinary_bladder|Cardiofaciocutaneous_syndrome_2|Hereditary_diffuse_gastric_adenocarcinoma|Carcinoma_of_pancreas|Cerebral_arteriovenous_malformation|Noonan_syndrome_3|Familial_cancer_of_breast|Cardiovascular_phenotype|Noonan_syndrome|Cardio-facio-cutaneous_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "Noonan_syndrome|RASopathy|not_provided|KRAS-related_disorder": 1,
    "Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Autoimmune_lymphoproliferative_syndrome_type_4|Malignant_tumor_of_urinary_bladder|Acute_myeloid_leukemia|Familial_cancer_of_breast|Noonan_syndrome_3|Cardiofaciocutaneous_syndrome_2|Familial_pancreatic_carcinoma|Gastric_cancer|Lung_cancer": 1,
    "RASopathy|not_provided|Noonan_syndrome_3|not_specified": 1,
    "Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Lung_cancer|Cardiofaciocutaneous_syndrome_2|Noonan_syndrome_3|Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Carcinoma_of_pancreas|Autoimmune_lymphoproliferative_syndrome_type_4|Acute_myeloid_leukemia|Familial_cancer_of_breast|Gastric_cancer|not_provided|RASopathy": 1,
    "Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Carcinoma_of_pancreas|Cardiofaciocutaneous_syndrome_2|Autoimmune_lymphoproliferative_syndrome_type_4|Acute_myeloid_leukemia|Lung_cancer|Noonan_syndrome_3|Familial_cancer_of_breast|Gastric_cancer|not_provided": 1,
    "not_provided|not_specified|KRAS-related_disorder": 1,
    "not_specified|KRAS-related_disorder": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4": 1,
    "not_provided|Cardio-facio-cutaneous_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "KRAS-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|KRAS-related_disorder|not_provided": 1,
    "KRAS-related_disorder|Noonan_syndrome_3": 1,
    "Noonan_syndrome_3|Familial_cancer_of_breast|Linear_nevus_sebaceous_syndrome|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Carcinoma_of_pancreas|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Lung_cancer|not_specified": 1,
    "RASopathy|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Cardiofaciocutaneous_syndrome_2|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Lung_cancer|Noonan_syndrome_3|Acute_myeloid_leukemia|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation": 1,
    "Cardiofaciocutaneous_syndrome_2|not_provided": 1,
    "OCULOECTODERMAL_SYNDROME|_SOMATIC|Familial_pancreatic_carcinoma|Malignant_tumor_of_urinary_bladder|not_provided|Encephalocraniocutaneous_lipomatosis|RASopathy": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4|Multiple_myeloma|RASopathy": 1,
    "Vascular_malformation|Encephalocraniocutaneous_lipomatosis|OCULOECTODERMAL_SYNDROME|_SOMATIC|Cardiofaciocutaneous_syndrome_2|not_provided|RASopathy|Classic_Hodgkin_lymphoma": 1,
    "not_provided|KRAS-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Cardiofaciocutaneous_syndrome_2|Autoimmune_lymphoproliferative_syndrome_type_4|Acute_myeloid_leukemia|Lung_cancer|Noonan_syndrome_3|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Gastric_cancer|not_provided|RASopathy|not_specified": 1,
    "Noonan_syndrome_3|Familial_cancer_of_breast|Linear_nevus_sebaceous_syndrome|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Carcinoma_of_pancreas|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Lung_cancer|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "RASopathy|Noonan_syndrome_3|Autoimmune_lymphoproliferative_syndrome_type_4|Familial_cancer_of_breast|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Familial_pancreatic_carcinoma|Gastric_cancer|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Lung_cancer": 2,
    "RASopathy|Cardiofaciocutaneous_syndrome_2|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Lung_cancer|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Cerebral_arteriovenous_malformation|Acute_myeloid_leukemia|Noonan_syndrome_3|Toriello-Lacassie-Droste_syndrome|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4|Cardiofaciocutaneous_syndrome_2|Acute_myeloid_leukemia|Noonan_syndrome_3|not_provided|KRAS-related_RASopathy": 1,
    "Colorectal_cancer|Encephalocraniocutaneous_lipomatosis|not_provided": 1,
    "Linear_nevus_sebaceous_syndrome": 1,
    "not_provided|Noonan_syndrome_1": 6,
    "RASopathy|Cardiofaciocutaneous_syndrome_2|Linear_nevus_sebaceous_syndrome|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Gastric_cancer|Acute_myeloid_leukemia|Autoimmune_lymphoproliferative_syndrome_type_4|Noonan_syndrome_3|Toriello-Lacassie-Droste_syndrome|Lung_cancer|Cerebral_arteriovenous_malformation": 1,
    "RASopathy|KRAS-related_disorder|not_specified": 1,
    "KRAS-related_disorder|not_provided|not_specified|RASopathy|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|RASopathy|not_provided|KRAS-related_disorder": 1,
    "Cardiovascular_phenotype|Sarcoma": 1,
    "Cardiofaciocutaneous_syndrome_2": 4,
    "Noonan_syndrome|not_provided|not_specified|RASopathy": 1,
    "Capillary_Telangiectasia|_Brain": 1,
    "Noonan_syndrome_3|Familial_cancer_of_breast|Linear_nevus_sebaceous_syndrome|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Familial_pancreatic_carcinoma|Lung_cancer|RASopathy": 1,
    "Noonan_syndrome_3|not_provided": 1,
    "Non-small_cell_lung_carcinoma|Vascular_malformation|Cerebral_arteriovenous_malformation": 1,
    "Colorectal_cancer|Cardiovascular_phenotype|not_provided|RASopathy|Non-small_cell_lung_carcinoma|Juvenile_myelomonocytic_leukemia": 1,
    "Multiple_myeloma|Non-small_cell_lung_carcinoma": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Lung_cancer|Noonan_syndrome": 1,
    "Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Non-small_cell_lung_carcinoma": 1,
    "Inborn_genetic_diseases|Cardio-facio-cutaneous_syndrome|Cardiofaciocutaneous_syndrome_2|Noonan_syndrome_3|not_provided|RASopathy|Noonan_syndrome|Toriello-Lacassie-Droste_syndrome": 1,
    "Noonan_syndrome_3|RASopathy|Cardiofaciocutaneous_syndrome_2|not_provided": 1,
    "Bladder_cancer|_transitional_cell|_somatic": 1,
    "Noonan_syndrome_3|not_provided|RASopathy|Noonan_syndrome": 1,
    "RASopathy|Cardiovascular_phenotype|Linear_nevus_sebaceous_syndrome|Familial_pancreatic_carcinoma|Autoimmune_lymphoproliferative_syndrome_type_4|Gastric_cancer|Cardiofaciocutaneous_syndrome_2|Familial_cancer_of_breast|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Acute_myeloid_leukemia|Noonan_syndrome_3|Lung_cancer": 1,
    "KRAS-related_disorder|not_provided": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4|Acute_myeloid_leukemia|Linear_nevus_sebaceous_syndrome|Noonan_syndrome_3|Cardiofaciocutaneous_syndrome_2|Gastric_cancer|Familial_cancer_of_breast|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Carcinoma_of_pancreas|Lung_cancer|RASopathy": 1,
    "Noonan_syndrome_3|Familial_cancer_of_breast|Linear_nevus_sebaceous_syndrome|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Carcinoma_of_pancreas|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Lung_cancer|not_specified|RASopathy": 1,
    "RASopathy|Noonan_syndrome_3": 1,
    "RASopathy|not_provided|Cardiofaciocutaneous_syndrome_1|Cardiovascular_phenotype|KRAS-related_disorder|Noonan_syndrome|Cardio-facio-cutaneous_syndrome": 1,
    "not_provided|Noonan_syndrome_3|RASopathy|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Acute_myeloid_leukemia|Autoimmune_lymphoproliferative_syndrome_type_4|Cardiofaciocutaneous_syndrome_2|Noonan_syndrome_3|Noonan_syndrome|Cardio-facio-cutaneous_syndrome|not_provided|RASopathy": 1,
    "KRAS-related_disorder": 4,
    "Cardiovascular_phenotype|KRAS-related_disorder|not_provided|RASopathy": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4|Familial_cancer_of_breast|Lung_cancer|Toriello-Lacassie-Droste_syndrome|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Carcinoma_of_pancreas|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Noonan_syndrome_3|Linear_nevus_sebaceous_syndrome|Gastric_cancer|not_specified|not_provided|RASopathy|Prostate_cancer|_hereditary|_1": 1,
    "Prostate_cancer|_hereditary|_1|not_specified": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4|Gastric_cancer|Toriello-Lacassie-Droste_syndrome|Linear_nevus_sebaceous_syndrome|Lung_cancer|Familial_pancreatic_carcinoma|Cardiofaciocutaneous_syndrome_2|Acute_myeloid_leukemia|Noonan_syndrome_3|Familial_cancer_of_breast|Malignant_tumor_of_urinary_bladder|Cerebral_arteriovenous_malformation|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "Vascular_malformation|Linear_nevus_sebaceous_syndrome|RASopathy|not_provided": 1,
    "RASopathy|OCULOECTODERMAL_SYNDROME|_SOMATIC|Encephalocraniocutaneous_lipomatosis": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Noonan_syndrome_3|Endometrial_carcinoma": 1,
    "Prostate_cancer|_hereditary|_1|Cardiovascular_phenotype|not_provided|Non-small_cell_lung_carcinoma": 1,
    "OCULOECTODERMAL_SYNDROME|_SOMATIC|Noonan_syndrome_and_Noonan-related_syndrome|KRAS-related_disorder|Inborn_genetic_diseases|Encephalocraniocutaneous_lipomatosis|Familial_pancreatic_carcinoma|not_provided|Nevus_sebaceous|RASopathy|Non-small_cell_lung_carcinoma|Autoimmune_lymphoproliferative_syndrome_type_4|Breast_adenocarcinoma|Juvenile_myelomonocytic_leukemia": 1,
    "Non-small_cell_lung_carcinoma|not_provided|Autoimmune_lymphoproliferative_syndrome_type_4|KRAS-related_disorder": 1,
    "Non-small_cell_lung_carcinoma|Pilocytic_astrocytoma|not_provided": 1,
    "Lung_sarcomatoid_carcinoma|not_provided|Linear_nevus_sebaceous_syndrome|Nevus_sebaceous|RASopathy|Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Carcinoma_of_pancreas|Cerebral_arteriovenous_malformation|Non-small_cell_lung_carcinoma|Juvenile_myelomonocytic_leukemia": 1,
    "Autoimmune_lymphoproliferative_syndrome_type_4|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Acute_myeloid_leukemia|Familial_pancreatic_carcinoma|Gastric_cancer|Familial_cancer_of_breast|Lung_cancer|Noonan_syndrome_3|Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Cardiofaciocutaneous_syndrome_2|Gallbladder_cancer|KRAS-related_disorder|not_provided|Multiple_myeloma|Non-small_cell_lung_carcinoma": 1,
    "Congenital_Pulmonary_Airway_Malformations|Cardiovascular_phenotype|Toriello-Lacassie-Droste_syndrome|Familial_pancreatic_carcinoma|Cardiofaciocutaneous_syndrome_2|Acute_myeloid_leukemia|Linear_nevus_sebaceous_syndrome|Noonan_syndrome_3|Familial_cancer_of_breast|Lung_cancer|Gastric_cancer|Autoimmune_lymphoproliferative_syndrome_type_4|Malignant_tumor_of_urinary_bladder|Cerebral_arteriovenous_malformation|Vascular_Tumors_Including_Pyogenic_Granuloma|Endometrial_hyperplasia_without_atypia|Atypical_endometrial_hyperplasia|Primary_low_grade_serous_adenocarcinoma_of_ovary|Encephalocraniocutaneous_lipomatosis|not_provided|Nevus_sebaceous|RASopathy|Ovarian_neoplasm|Carcinoma_of_pancreas|Epidermal_nevus|Capillary_malformation-arteriovenous_malformation_1|Non-small_cell_lung_carcinoma|Juvenile_myelomonocytic_leukemia": 1,
    "Lung_carcinoma|RASopathy|Endometrial_carcinoma|Lung_adenocarcinoma|Non-small_cell_lung_carcinoma|Gallbladder_cancer|Lung_cancer|not_provided": 1,
    "not_provided|RASopathy|Malignant_tumor_of_urinary_bladder|Non-small_cell_lung_carcinoma|Squamous_cell_lung_carcinoma": 1,
    "Vascular_malformation|Gastric_cancer|Cardiofaciocutaneous_syndrome_2|not_provided|RASopathy|Ovarian_neoplasm|Non-small_cell_lung_carcinoma|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Noonan_syndrome_3|Acute_myeloid_leukemia|Cardiofaciocutaneous_syndrome_2|Linear_nevus_sebaceous_syndrome|Toriello-Lacassie-Droste_syndrome|Familial_cancer_of_breast|Lung_cancer|Carcinoma_of_pancreas|Gastric_cancer|Cerebral_arteriovenous_malformation|Malignant_tumor_of_urinary_bladder|Autoimmune_lymphoproliferative_syndrome_type_4|RASopathy": 1,
    "Inborn_genetic_diseases|Cardiofaciocutaneous_syndrome_2|not_provided|RASopathy": 1,
    "KRAS-related_disorder|not_provided|RASopathy|Noonan_syndrome|Prostate_cancer|_hereditary|_1|Noonan_syndrome_3": 1,
    "KRAS-related_disorder|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "BHLHE41-related_disorder": 8,
    "Short_sleep|_familial_natural|_1": 2,
    "not_specified|BHLHE41-related_disorder": 1,
    "Isolated_anhidrosis_with_normal_sweat_glands": 5,
    "not_provided|Isolated_anhidrosis_with_normal_sweat_glands": 1,
    "ITPR2-related_disorder": 18,
    "not_specified|not_provided|ITPR2-related_disorder": 2,
    "Isolated_anhidrosis_with_normal_sweat_glands|not_provided": 7,
    "ITPR2-related_disorder|not_provided": 2,
    "STK38L-related_disorder": 3,
    "STK38L-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_seizures|_microcephaly|_and_brain_abnormalities": 5,
    "Cerebral_calcification|Intellectual_disability|_severe|Seizure|Microcephaly|Neurodevelopmental_disorder_with_seizures|_microcephaly|_and_brain_abnormalities": 2,
    "Intellectual_disability|_severe|Seizure|Cerebral_calcification|Microcephaly|Neurodevelopmental_disorder_with_seizures|_microcephaly|_and_brain_abnormalities": 1,
    "Cerebral_calcification|Intellectual_disability|_severe|Seizure|Microcephaly": 4,
    "Neurodevelopmental_disorder_with_seizures|_microcephaly|_and_brain_abnormalities|Cerebral_calcification|Intellectual_disability|_severe|Seizure|Microcephaly": 2,
    "Neurodevelopmental_disorder_with_seizures|_microcephaly|_and_brain_abnormalities|Seizure|Intellectual_disability|_severe|Microcephaly|Cerebral_calcification": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_seizures|_microcephaly|_and_brain_abnormalities": 1,
    "PPFIBP1-related_disorder": 1,
    "Brachydactyly_type_E2": 10,
    "PTHLH-related_disorder": 2,
    "not_provided|PTHLH-related_disorder": 1,
    "Brachydactyly_type_E2|not_provided": 1,
    "Inborn_genetic_diseases|IPO8-related_disorder": 1,
    "not_provided|IPO8_related_Connective_tissue_disorder|VISS_syndrome|IPO8-related_aortopathy": 1,
    "IPO8-related_disorder": 4,
    "VISS_syndrome": 9,
    "IPO8_related_Connective_tissue_disorder": 3,
    "IPO8-related_aortopathy|VISS_syndrome": 2,
    "Duane-radial_ray_syndrome|VISS_syndrome": 1,
    "VISS_syndrome|IPO8_related_Connective_tissue_disorder": 6,
    "VISS_syndrome|not_provided|IPO8_related_Connective_tissue_disorder": 1,
    "IPO8-related_aortopathy": 3,
    "not_provided|VISS_syndrome": 1,
    "VISS_syndrome|IPO8-related_aortopathy": 1,
    "IPO8-related_aortopathy|not_provided": 1,
    "not_provided|VISS_syndrome|IPO8-related_disorder": 1,
    "Inborn_genetic_diseases|VISS_syndrome": 1,
    "Warsaw_breakage_syndrome": 47,
    "Warsaw_breakage_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Warsaw_breakage_syndrome|not_provided": 14,
    "not_provided|Warsaw_breakage_syndrome": 7,
    "DDX11-related_condition|not_provided|Warsaw_breakage_syndrome": 1,
    "not_specified|not_provided|Warsaw_breakage_syndrome": 1,
    "Inborn_genetic_diseases|Warsaw_breakage_syndrome|not_provided": 1,
    "DENND5B-related_neurodevelopmental_disorder|not_provided": 1,
    "DENND5B_related_condition|DENND5B-related_neurodevelopmental_disorder": 1,
    "DENND5B-related_neurodevelopmental_disorder": 4,
    "Charcot-Marie-Tooth_disease_type_4H|not_provided": 14,
    "Charcot-Marie-Tooth_disease_type_4H": 119,
    "not_provided|Charcot-Marie-Tooth_disease_type_4H": 18,
    "FGD4-related_disorder|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4H|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H": 3,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|FGD4-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|FGD4-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease_type_4H|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4H|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|FGD4-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4H": 9,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4H": 2,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4": 8,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H": 1,
    "not_provided|not_specified|FGD4-related_disorder|Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|FGD4-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4H|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease": 3,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 2,
    "FGD4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|FGD4-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4H": 2,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_provided|not_specified|FGD4-related_disorder|Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4H|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Inborn_genetic_diseases|FGD4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4H": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4H|FGD4-related_disorder|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4H|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4H|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "FGD4-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4H": 1,
    "FGD4-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4H": 1,
    "Optic_atrophy_5": 2,
    "not_provided|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1": 4,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|not_provided": 2,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|DNM1L-related_disorder|not_provided": 2,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|not_provided|Optic_atrophy_5|not_specified": 1,
    "Encephalopathy_due_to_mitochondrial_and_peroxisomal_fission_defect": 1,
    "DNM1L-related_disorder": 6,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|not_specified|not_provided|Optic_atrophy_5": 1,
    "Inborn_genetic_diseases|not_provided|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5|not_specified": 1,
    "Inborn_genetic_diseases|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1": 2,
    "not_provided|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5|not_specified": 1,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5": 1,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|not_provided|not_specified|Optic_atrophy_5": 1,
    "DNM1L-related_disorder|not_provided": 2,
    "not_provided|not_specified|DNM1L-related_disorder": 2,
    "DNM1L-related_disorder|not_specified|not_provided": 1,
    "Mitochondrial_disease|DNM1L-related_disorder": 1,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5|Inborn_genetic_diseases|not_provided": 1,
    "Optic_atrophy_5|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1": 1,
    "not_provided|Optic_atrophy_5": 1,
    "Optic_atrophy_5|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|not_provided": 1,
    "not_provided|DNM1L-related_disorder": 1,
    "not_provided|Lethal_Encephalopathy": 3,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1": 1,
    "Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|DNM1L-related_disorder": 1,
    "DNM1L-related_movement_disorder|not_provided": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Encephalopathy|_lethal|_due_to_defective_mitochondrial_peroxisomal_fission_1|Optic_atrophy_5|not_provided": 2,
    "Lethal_Encephalopathy|not_provided": 2,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|not_provided": 2,
    "Lethal_Encephalopathy": 7,
    "Lethal_Encephalopathy|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Lethal_Encephalopathy|not_provided": 2,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_provided": 1,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 2,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Lethal_Encephalopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 2,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Lethal_Encephalopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_provided": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 16,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Lethal_Encephalopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 3,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Lethal_Encephalopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 3,
    "Lethal_Encephalopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 2,
    "Lethal_Encephalopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 1,
    "YARS2-related_disorder": 2,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis": 1,
    "not_provided|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_specified|not_provided": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|YARS2-related_disorder|not_specified": 1,
    "YARS2-related_disorder|not_provided": 3,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 3,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 6,
    "not_provided|YARS2-related_disorder": 4,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|YARS2-related_disorder|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 2,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_specified": 1,
    "YARS2-related_disorder|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|not_provided": 1,
    "not_specified|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "not_provided|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|YARS2-related_disorder|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_specified": 1,
    "YARS2-related_disorder|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|not_specified|not_provided": 1,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "YARS2-related_disorder|not_specified|not_provided|Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2": 1,
    "Hereditary_Sideroblastic_Anemia_with_Myopathy_and_Lactic_Acidosis|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_2|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 21,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 37,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 27,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 42,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 10,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 24,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 10,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 45,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 4,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder|not_specified": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified": 15,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 19,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 6,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 2,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|PKP2-related_disorder|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 7,
    "Cardiovascular_phenotype|Ventricular_tachycardia|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 8,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 8,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype": 6,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 3,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|not_specified": 3,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 4,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_ventricular_cardiomyopathy|Cardiovascular_phenotype|Sudden_unexplained_death|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 4,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 5,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Dilated_cardiomyopathy_1A": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 8,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 9,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 5,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 9,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 12,
    "PKP2-related_disorder|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy|Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 42,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Cardiovascular_phenotype|PKP2-related_disorder|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 3,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 6,
    "Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 3,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy|PKP2-related_disorder|not_specified": 1,
    "PKP2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 7,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "Cardiovascular_phenotype|PKP2-related_disorder|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 6,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|not_provided": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 27,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 6,
    "PKP2-related_disorder|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 6,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 4,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 7,
    "Cardiomyopathy|PKP2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1S|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Left_ventricular_noncompaction|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 4,
    "PKP2-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 8,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified": 2,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 4,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|PKP2-related_disorder|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 3,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|PKP2-related_disorder|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Ventricular_tachycardia": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|PKP2-related_disorder|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "PKP2-related_disorder|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|PKP2-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Family_history_of_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Brugada_syndrome|Premature_ventricular_contraction|not_provided|not_specified|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "PKP2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype": 7,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 5,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|PKP2-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Brugada_syndrome|Dilated_cardiomyopathy_3B|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "PKP2-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "PKP2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|PKP2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|PKP2-related_disorder|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|PKP2-related_disorder|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "PKP2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|PKP2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiac_arrhythmia|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|PKP2-related_disorder|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|PKP2-related_disorder": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "PKP2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|PKP2-related_disorder|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Left_ventricular_noncompaction_1|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "Ventricular_tachycardia|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|PKP2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|PKP2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_9|Ventricular_fibrillation|not_specified|Amyloidosis|_hereditary_systemic_1|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_provided|Arrhythmogenic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|PKP2-related_disorder|Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_specified|PKP2-related_disorder|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_9|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy|not_provided|PKP2-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Conduction_disorder_of_the_heart|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Sudden_unexplained_death|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiac_arrhythmia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|AV_junctional_rhythm|Ventricular_tachycardia": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "not_provided|PKP2-related_disorder|not_specified|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|PKP2-related_disorder|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "PKP2-related_disorder|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 3,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Sudden_cardiac_death": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|not_specified": 1,
    "Cardiac_arrhythmia|not_provided|Arrhythmogenic_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_36": 765,
    "ALG10-related_disorder": 2,
    "ALG10-related_disorder|not_provided": 1,
    "Congenital_fibrosis_of_extraocular_muscles_type_1": 83,
    "Congenital_fibrosis_of_extraocular_muscles|not_provided": 2,
    "Congenital_fibrosis_of_extraocular_muscles_type_1|not_provided": 16,
    "Congenital_fibrosis_of_extraocular_muscles_type_1|Inborn_genetic_diseases": 5,
    "KIF21A-related_disorder|Congenital_fibrosis_of_extraocular_muscles_type_1|not_provided": 2,
    "Congenital_fibrosis_of_extraocular_muscles_type_1|KIF21A-related_disorder|not_provided": 2,
    "KIF21A-related_disorder": 8,
    "Congenital_fibrosis_of_extraocular_muscles_type_1|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Congenital_fibrosis_of_extraocular_muscles_type_1": 4,
    "not_provided|Congenital_fibrosis_of_extraocular_muscles_type_1|KIF21A-related_disorder": 2,
    "Congenital_fibrosis_of_extraocular_muscles|KIF21A-related_disorder": 1,
    "Abnormality_of_eye_movement|not_provided|Fibrosis_of_extraocular_muscles|_congenital|_3b|Congenital_fibrosis_of_extraocular_muscles_type_1": 1,
    "KIF21A-related_disorder|not_provided|Congenital_fibrosis_of_extraocular_muscles_type_1|Fibrosis_of_extraocular_muscles|_congenital|_3b": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_3b": 1,
    "Inborn_genetic_diseases|Congenital_fibrosis_of_extraocular_muscles_type_1|KIF21A-related_disorder|not_provided": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_3b|not_provided": 1,
    "Inborn_genetic_diseases|KIF21A-related_disorder": 1,
    "Congenital_fibrosis_of_extraocular_muscles_type_1|Congenital_fibrosis_of_extraocular_muscles|Inborn_genetic_diseases": 1,
    "KIF21A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KIF21A-related_disorder|not_provided": 1,
    "Congenital_fibrosis_of_extraocular_muscles_type_1|not_specified|not_provided": 1,
    "not_provided|Congenital_fibrosis_of_extraocular_muscles_type_1": 4,
    "not_provided|KIF21A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_Parkinson_disease_8": 36,
    "Autosomal_dominant_Parkinson_disease_8": 480,
    "Inborn_genetic_diseases|Autosomal_dominant_Parkinson_disease_8": 129,
    "Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases": 151,
    "not_specified|Autosomal_dominant_Parkinson_disease_8": 8,
    "Autosomal_dominant_Parkinson_disease_8|not_specified|not_provided": 10,
    "LRRK2-related_disorder": 5,
    "Inborn_genetic_diseases|Autosomal_dominant_Parkinson_disease_8|not_provided": 4,
    "Autosomal_dominant_Parkinson_disease_8|not_provided": 37,
    "Autosomal_dominant_Parkinson_disease_8|not_provided|not_specified": 5,
    "not_provided|Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases": 5,
    "LRRK2-related_disorder|Autosomal_dominant_Parkinson_disease_8": 4,
    "not_provided|Autosomal_dominant_Parkinson_disease_8|not_specified": 8,
    "Autosomal_dominant_Parkinson_disease_8|not_provided|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_Parkinson_disease_8": 8,
    "LRRK2-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_dominant_Parkinson_disease_8": 1,
    "Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases|LRRK2-related_disorder": 1,
    "not_specified|not_provided|Autosomal_dominant_Parkinson_disease_8": 6,
    "Inborn_genetic_diseases|LRRK2-related_disorder": 3,
    "not_specified|Autosomal_dominant_Parkinson_disease_8|not_provided": 4,
    "Autosomal_dominant_Parkinson_disease_8|LRRK2-related_disorder|not_provided": 2,
    "Autosomal_dominant_Parkinson_disease_8|not_specified": 2,
    "not_provided|Autosomal_dominant_Parkinson_disease_8|LRRK2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_Parkinson_disease_8|LRRK2-related_disorder": 4,
    "not_specified|not_provided|Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases": 1,
    "LRRK2-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_Parkinson_disease_8": 3,
    "not_specified|Parkinsonian_disorder|Parkinson_disease|Vascular_parkinsonism": 1,
    "Autosomal_dominant_Parkinson_disease_8|LRRK2-related_disorder|Inborn_genetic_diseases": 2,
    "Parkinson_disease|_late-onset|Autosomal_dominant_Parkinson_disease_8": 1,
    "LRRK2-related_disorder|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_Parkinson_disease_8|LRRK2-related_disorder": 3,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_Parkinson_disease_8": 1,
    "not_provided|LRRK2-related_disorder|Autosomal_dominant_Parkinson_disease_8|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Parkinson_disease_8|not_provided|LRRK2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_Parkinson_disease_8": 1,
    "Inborn_genetic_diseases|LRRK2-related_disorder|Autosomal_dominant_Parkinson_disease_8": 1,
    "Parkinson_disease|not_provided": 1,
    "Autosomal_dominant_Parkinson_disease_8|Parkinson_disease|_late-onset": 1,
    "LRRK2-related_disorder|not_provided|Autosomal_dominant_Parkinson_disease_8": 1,
    "Inborn_genetic_diseases|LRRK2-related_disorder|Autosomal_dominant_Parkinson_disease_8|not_provided": 1,
    "Autosomal_dominant_Parkinson_disease_8|Parkinson_disease|not_provided|Early_onset_Alzheimer_disease_with_behavioral_disturbance|Klippel-Feil_syndrome_1|_autosomal_dominant|Spinocerebellar_atrophy": 1,
    "Interstitial_pulmonary_disease": 1,
    "Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases|LRRK2-related_disorder|not_provided": 1,
    "Autosomal_dominant_Parkinson_disease_8|LRRK2-related_disorder|Parkinson_Disease|_Dominant|not_specified|not_provided": 1,
    "Parkinsonian_disorder|Brain_atrophy|Frontotemporal_dementia|Rigidity|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_dominant_Parkinson_disease_8|not_specified|Inborn_genetic_diseases": 1,
    "LRRK2-related_disorder|Young-onset_Parkinson_disease|Inborn_genetic_diseases|not_provided|Parkinson_disease|Autosomal_dominant_Parkinson_disease_8|Parkinson_disease|_late-onset": 1,
    "Vascular_parkinsonism|Parkinson_disease|Parkinsonian_disorder|not_specified|not_provided|Autosomal_dominant_Parkinson_disease_8": 1,
    "Autosomal_dominant_Parkinson_disease_8|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Autosomal_dominant_Parkinson_disease_8|not_provided|Parkinson_disease": 1,
    "Autosomal_dominant_Parkinson_disease_8|Leprosy|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Compton-North_congenital_myopathy": 413,
    "not_provided|Compton-North_congenital_myopathy": 11,
    "not_specified|Compton-North_congenital_myopathy|not_provided": 2,
    "Inborn_genetic_diseases|Compton-North_congenital_myopathy": 25,
    "Compton-North_congenital_myopathy|not_provided": 14,
    "not_specified|not_provided|Compton-North_congenital_myopathy": 8,
    "CNTN1-related_disorder": 4,
    "not_specified|Compton-North_congenital_myopathy": 5,
    "Compton-North_congenital_myopathy|not_specified": 6,
    "Compton-North_congenital_myopathy|not_specified|not_provided": 3,
    "not_provided|Compton-North_congenital_myopathy|not_specified": 2,
    "Compton-North_congenital_myopathy|Inborn_genetic_diseases": 17,
    "Inborn_genetic_diseases|Compton-North_congenital_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|Compton-North_congenital_myopathy|not_specified|not_provided": 1,
    "Compton-North_congenital_myopathy|CNTN1-related_disorder|not_provided": 3,
    "CNTN1-related_disorder|not_provided|Compton-North_congenital_myopathy": 1,
    "CNTN1-related_disorder|Compton-North_congenital_myopathy": 1,
    "Compton-North_congenital_myopathy|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Compton-North_congenital_myopathy": 2,
    "not_provided|Compton-North_congenital_myopathy|Inborn_genetic_diseases": 2,
    "Compton-North_congenital_myopathy|not_provided|Inborn_genetic_diseases": 3,
    "Compton-North_congenital_myopathy|not_provided|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Compton-North_congenital_myopathy": 1,
    "GXYLT1-related_disorder": 2,
    "Epilepsy|_progressive_myoclonic|_1B": 361,
    "not_provided|Epilepsy|_progressive_myoclonic|_1B": 14,
    "Epilepsy|_progressive_myoclonic|_1B|not_specified|not_provided": 3,
    "not_specified|not_provided|Epilepsy|_progressive_myoclonic|_1B": 14,
    "not_specified|Seizure|Epilepsy|_progressive_myoclonic|_1B": 1,
    "PRICKLE1-related_disorder|Epilepsy|_progressive_myoclonic|_1B|not_specified": 3,
    "Epilepsy|_progressive_myoclonic|_1B|not_specified": 36,
    "PRICKLE1-related_disorder|not_provided|not_specified|Epilepsy|_progressive_myoclonic|_1B": 1,
    "PRICKLE1-related_disorder": 2,
    "not_specified|Intellectual_disability|not_provided|Epilepsy|_progressive_myoclonic|_1B|Self-limited_epilepsy_with_centrotemporal_spikes": 1,
    "not_specified|Epilepsy|_progressive_myoclonic|_1B": 24,
    "not_specified|Epilepsy|_progressive_myoclonic|_1B|not_provided": 2,
    "Epilepsy|_progressive_myoclonic|_1B|not_provided|not_specified": 6,
    "not_specified|PRICKLE1-related_disorder|not_provided|Epilepsy|_progressive_myoclonic|_1B": 2,
    "not_provided|Epilepsy|_progressive_myoclonic|_1B|not_specified": 5,
    "not_provided|not_specified|Epilepsy|_progressive_myoclonic|_1B|PRICKLE1-related_disorder": 1,
    "not_specified|PRICKLE1-related_disorder|Epilepsy|_progressive_myoclonic|_1B": 2,
    "not_provided|not_specified|Epilepsy|_progressive_myoclonic|_1B": 3,
    "PRICKLE1-related_disorder|not_specified|not_provided|Epilepsy|_progressive_myoclonic|_1B": 6,
    "Epilepsy|_progressive_myoclonic|_1B|Inborn_genetic_diseases": 1,
    "Epilepsy|_progressive_myoclonic|_1B|not_provided": 7,
    "PRICKLE1-related_disorder|not_provided|Epilepsy|_progressive_myoclonic|_1B|not_specified": 1,
    "not_specified|Intellectual_disability|not_provided|Epilepsy|_progressive_myoclonic|_1B": 1,
    "not_specified|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Epilepsy|_progressive_myoclonic|_1B": 1,
    "Epilepsy|_progressive_myoclonic|_1B|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided": 1,
    "Epilepsy|_progressive_myoclonic|_1B|Intellectual_disability": 1,
    "ADAMTS20-related_condition": 3,
    "Immunodeficiency_67": 266,
    "Immunodeficiency_67|not_provided": 4,
    "Congenital_dyserythropoietic_anemia": 16,
    "Immunodeficiency_67|IRAK4-related_disorder": 1,
    "Inborn_genetic_diseases|Immunodeficiency_67": 10,
    "not_provided|Immunodeficiency_67": 15,
    "Immunodeficiency_67|Inborn_genetic_diseases": 3,
    "IRAK4-related_disorder|not_provided|Immunodeficiency_67": 1,
    "not_provided|Inborn_genetic_diseases|Immunodeficiency_67": 1,
    "IRAK4-related_disorder|Immunodeficiency_67|not_provided": 1,
    "not_provided|Immunodeficiency_67|IRAK4-related_disorder": 1,
    "Invasive_pneumococcal_disease|_recurrent_isolated|Immunodeficiency_67": 1,
    "not_specified|not_provided|Immunodeficiency_67": 1,
    "Inborn_genetic_diseases|ANO6-related_disorder": 2,
    "not_provided|not_specified|ANO6-related_disorder": 1,
    "ANO6-related_disorder|not_provided|not_specified": 2,
    "ANO6-related_disorder": 7,
    "ANO6-related_disorder|not_provided": 3,
    "SCOTT_SYNDROME": 8,
    "not_provided|ANO6-related_disorder": 3,
    "SCOTT_SYNDROME|not_provided": 1,
    "ANO6-related_disorder|SCOTT_SYNDROME|not_provided": 1,
    "not_provided|ANO6-related_disorder|not_specified": 1,
    "SCOTT_SYNDROME|not_provided|ANO6-related_disorder": 1,
    "not_provided|SCOTT_SYNDROME": 1,
    "ARID2-related_disorder": 18,
    "not_specified|not_provided|Microcephaly": 1,
    "Coffin-Siris_syndrome_6|ARID2-related_disorder": 1,
    "ARID2-related_BAFopathy": 6,
    "Coffin-Siris_syndrome_6|not_provided": 6,
    "Coffin-Siris_syndrome_6|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Coffin-Siris_syndrome_6": 2,
    "not_provided|ARID2-related_BAFopathy|Coffin-Siris_syndrome_6": 1,
    "Inborn_genetic_diseases|ARID2-related_disorder|Coffin-Siris_syndrome_6|not_specified|not_provided": 1,
    "ARID2-related_disorder|not_provided": 2,
    "not_specified|Coffin-Siris_syndrome_6|not_provided": 1,
    "Desmoplastic/nodular_medulloblastoma": 1,
    "Inborn_genetic_diseases|ARID2-related_disorder": 1,
    "ARID2-related_disorder|not_specified|not_provided": 3,
    "not_provided|ARID2-related_disorder": 2,
    "not_specified|ARID2-related_disorder|not_provided": 2,
    "See_cases|Coffin-Siris_syndrome": 1,
    "not_provided|Coffin-Siris_syndrome_6": 3,
    "ARID2-related_disorder|Inborn_genetic_diseases|See_cases": 1,
    "ARID2-related_disorder|Coffin-Siris_syndrome_6|not_specified|not_provided": 1,
    "not_provided|ARID2-related_disorder|Inborn_genetic_diseases": 1,
    "ARID2-related_disorder|Coffin-Siris_syndrome_6": 1,
    "ARID2-related_BAFopathy|Coffin-Siris_syndrome_6": 1,
    "Chronic_diarrhea": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia": 141,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided": 29,
    "Vitamin_D-dependent_rickets": 13,
    "not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia": 30,
    "Vitamin_D-dependent_rickets|not_provided": 1,
    "Periodontitis|not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia": 2,
    "not_provided|Vitamin_D-dependent_rickets": 2,
    "Periodontitis|Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided": 1,
    "VDR-related_disorder|not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia": 2,
    "VDR-related_disorder|Vitamin_D-dependent_rickets_type_II_with_alopecia": 1,
    "VDR-related_disorder|not_provided": 3,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia": 2,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_specified|not_provided": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided|not_specified": 1,
    "not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia|not_specified|VDR-related_disorder": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided|Hepatocellular_carcinoma|Periodontitis|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Vitamin_D-dependent_rickets_type_II_with_alopecia": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|Periodontitis|not_provided|Hepatocellular_carcinoma": 1,
    "not_provided|Periodontitis|Hepatocellular_carcinoma": 1,
    "not_specified|Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided": 1,
    "not_provided|not_specified|Vitamin_D-dependent_rickets_type_II_with_alopecia": 2,
    "not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Vitamin_D-dependent_rickets_type_II_with_alopecia": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|Rickets|not_provided": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided|Familial_adenomatous_polyposis_2": 1,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided|VDR-related_disorder": 1,
    "not_provided|VDR-related_disorder": 2,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided": 3,
    "Vitamin_D-dependent_rickets_type_II_with_alopecia|not_provided|Inborn_genetic_diseases": 3,
    "VDR-related_disorder": 1,
    "VDR-related_disorder|Vitamin_D-dependent_rickets_type_II_with_alopecia|not_specified|not_provided": 1,
    "Periodontitis|not_provided|not_specified|Vitamin_D-dependent_rickets_type_II_with_alopecia": 1,
    "Stickler_syndrome_type_1|Type_II_Collagenopathies": 7,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1": 6,
    "not_provided|Stickler_syndrome_type_1|Type_II_Collagenopathies": 5,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1|not_provided": 6,
    "Stickler_syndrome_type_1|Type_II_Collagenopathies|not_provided": 11,
    "Type_II_Collagenopathies|not_provided|Stickler_syndrome_type_1": 4,
    "not_specified|Type_II_Collagenopathies|Stickler_syndrome_type_1|Connective_tissue_disorder|not_provided": 2,
    "Stickler_syndrome|_type_I|_nonsyndromic_ocular": 13,
    "Spondyloepiphyseal_dysplasia_congenita|not_provided": 5,
    "not_provided|Spondyloperipheral_dysplasia": 2,
    "COL2A1-related_disorder|not_provided": 32,
    "Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloepiphyseal_dysplasia_congenita|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Legg-Calve-Perthes_disease|Kniest_dysplasia|COL2A1-related_disorder|not_provided": 1,
    "Platyspondylic_dysplasia|_Torrance_type": 4,
    "COL2A1-related_disorder": 41,
    "not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 6,
    "not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1|COL2A1-related_disorder": 1,
    "Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_congenita|Spondyloperipheral_dysplasia|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Avascular_necrosis_of_femoral_head|_primary|_1|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|not_provided": 1,
    "Achondrogenesis_type_II": 25,
    "not_provided|not_specified|Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Namaqualand_hip_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloperipheral_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Stickler_syndrome_type_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Connective_tissue_disorder|Type_II_Collagenopathies": 1,
    "Stickler_syndrome_type_1|not_provided": 20,
    "Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloperipheral_dysplasia": 1,
    "not_provided|COL2A1-related_disorder": 35,
    "Spondyloperipheral_dysplasia": 15,
    "Stickler_syndrome_type_1": 64,
    "Spondyloperipheral_dysplasia|not_provided|COL2A1-related_disorder|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Achondrogenesis_type_II|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloperipheral_dysplasia|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Legg-Calve-Perthes_disease|Kniest_dysplasia|Stickler_syndrome_type_1|not_provided": 1,
    "Stickler_syndrome_type_1|not_provided|Type_II_Collagenopathies": 6,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1|not_specified|not_provided": 6,
    "Spondyloperipheral_dysplasia|Platyspondylic_dysplasia|_Torrance_type|not_provided": 1,
    "Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia_congenita|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Stickler_syndrome_type_1|Spondyloperipheral_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia": 5,
    "COL2A1-related_disorder|not_provided|Avascular_necrosis_of_femoral_head|_primary|_1": 1,
    "Achondrogenesis_type_II|not_provided": 4,
    "Spondyloepiphyseal_dysplasia_congenita": 29,
    "Connective_tissue_disorder|Stickler_syndrome_type_1|Type_II_Collagenopathies|not_provided": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 3,
    "Connective_tissue_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1|not_specified": 3,
    "not_provided|Stickler_syndrome_type_1": 27,
    "Inborn_genetic_diseases|not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 1,
    "not_provided|Type_2_collagenopathy": 4,
    "Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloperipheral_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloepiphyseal_dysplasia_congenita|Legg-Calve-Perthes_disease|Kniest_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|not_provided": 1,
    "not_provided|MASS_syndrome": 2,
    "COL2A1-related_skeletal_dysplasia": 1,
    "MASS_syndrome": 5,
    "not_specified|not_provided|COL2A1-related_disorder": 1,
    "not_provided|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia": 1,
    "COL2A1-related_disorder|Stickler_syndrome_type_1|not_provided": 3,
    "Stickler_syndrome_type_1|COL2A1-related_disorder|Connective_tissue_disorder|not_provided|Type_II_Collagenopathies": 1,
    "Stickler_syndrome_type_1|not_specified|Type_II_Collagenopathies|not_provided|Connective_tissue_disorder": 1,
    "not_provided|Type_II_Collagenopathies|Connective_tissue_disorder|Stickler_syndrome_type_1": 1,
    "COL2A1-related_disorder|Connective_tissue_disorder|not_provided|Stickler_syndrome_type_1|Type_II_Collagenopathies": 1,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Spondyloepiphyseal_dysplasia|_Stanescu_type|Platyspondylic_dysplasia|_Torrance_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type": 3,
    "not_provided|Abnormal_cartilage_collagen": 1,
    "Spondyloepiphyseal_dysplasia|_Stanescu_type|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|COL2A1-related_disorder": 1,
    "Type_2_collagenopathy": 4,
    "Stickler_syndrome|not_provided|COL2A1-related_disorder": 1,
    "not_provided|Spondyloepiphyseal_dysplasia_congenita": 8,
    "Connective_tissue_disorder|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Inborn_genetic_diseases|not_provided|Type_2_collagenopathy|Stickler_syndrome_type_1|Spondyloepiphyseal_dysplasia_congenita|Spondyloperipheral_dysplasia|Namaqualand_hip_dysplasia": 1,
    "not_provided|Achondrogenesis_type_II": 6,
    "Spondyloepiphyseal_dysplasia_congenita|not_provided|COL2A1-related_disorder": 1,
    "Spondyloepiphyseal_dysplasia|_Stanescu_type": 7,
    "Type_II_Collagenopathies|not_provided|Stickler_Syndrome|_Dominant": 1,
    "Spondyloepimetaphyseal_dysplasia|_Strudwick_type": 9,
    "Type_II_Collagenopathies|not_provided|Stickler_syndrome_type_1|not_specified": 1,
    "Kniest_dysplasia|Stickler_syndrome_type_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepiphyseal_dysplasia_congenita|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloperipheral_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|not_provided": 1,
    "COL2A1-related_disorder|Platyspondylic_dysplasia|_Torrance_type|not_provided": 1,
    "Disproportionate_short-limb_short_stature|Narrow_chest|Achondrogenesis_type_II": 1,
    "Spondyloperipheral_dysplasia|not_provided": 2,
    "Spondyloepiphyseal_dysplasia_congenita|COL2A1-related_skeletal_dysplasia": 1,
    "Type_II_Collagenopathies": 1,
    "Stickler_syndrome_type_1|Marfan_syndrome|not_provided": 1,
    "Kniest_dysplasia": 14,
    "Kniest_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Spondyloepiphyseal_dysplasia_congenita|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Osteoarthritis|not_provided": 1,
    "not_provided|Type_II_Collagenopathies|not_specified|Stickler_syndrome_type_1|COL2A1-related_disorder": 1,
    "Stickler_syndrome_type_1|not_specified|Type_II_Collagenopathies|not_provided|COL2A1-related_disorder": 1,
    "not_provided|Stickler_syndrome_type_1|Spondyloperipheral_dysplasia": 1,
    "not_provided|Inborn_genetic_diseases|Stickler_syndrome_type_1|Type_II_Collagenopathies|Intellectual_disability": 1,
    "Spondylometaphyseal_dysplasia|_Schmidt_type|not_provided|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Avascular_necrosis_of_femoral_head|_primary|_1|Namaqualand_hip_dysplasia|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Legg-Calve-Perthes_disease|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Inborn_genetic_diseases|not_provided": 1,
    "Hypochondrogenesis": 3,
    "not_provided|Achondrogenesis_type_II|COL2A1-related_disorder": 1,
    "not_provided|Type_II_Collagenopathies|not_specified|Stickler_syndrome_type_1": 1,
    "Congenital_aneurysm_of_ascending_aorta": 3,
    "Achondrogenesis_type_II|not_specified": 1,
    "not_provided|Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_congenita|Namaqualand_hip_dysplasia|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Stickler_syndrome_type_1|Spondyloperipheral_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Avascular_necrosis_of_femoral_head|_primary|_1|Type_2_collagenopathy": 1,
    "not_provided|Stickler_syndrome_type_1|COL2A1-related_disorder|Type_II_Collagenopathies|not_specified": 1,
    "not_provided|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Achondrogenesis_type_II|Legg-Calve-Perthes_disease|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular": 1,
    "Type_II_Collagenopathies|not_specified|Stickler_syndrome_type_1|Connective_tissue_disorder|not_provided": 2,
    "not_provided|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepiphyseal_dysplasia|_Stanescu_type|Multiple_epiphyseal_dysplasia|_Beighton_type|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia_congenita|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepimetaphyseal_dysplasia|_Strudwick_type": 1,
    "Mendelian_syndromes_with_cleft_lip/palate|Type_II_Collagenopathies|COL2A1-related_disorder|not_provided|Stickler_syndrome_type_1": 1,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Legg-Calve-Perthes_disease|Kniest_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepiphyseal_dysplasia_congenita|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Spondyloperipheral_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1": 1,
    "Achondrogenesis_type_II|not_provided|Short_ribs|Absent_vertebral_body_mineralization": 1,
    "not_provided|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Namaqualand_hip_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Type_II_Collagenopathies|not_specified|not_provided|Stickler_syndrome_type_1": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Strudwick_type": 1,
    "not_provided|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloperipheral_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Kniest_dysplasia|Multiple_epiphyseal_dysplasia|_Beighton_type|Achondrogenesis_type_II|Legg-Calve-Perthes_disease|Spondylometaphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome_type_1|Namaqualand_hip_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Kniest_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia_congenita|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia|_Stanescu_type|not_provided": 2,
    "Multiple_epiphyseal_dysplasia|_Beighton_type": 2,
    "Connective_tissue_disorder|not_provided|Stickler_syndrome_type_1|Type_II_Collagenopathies": 1,
    "Achondrogenesis_type_II|Avascular_necrosis_of_femoral_head|_primary|_1|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia_congenita|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Legg-Calve-Perthes_disease|Kniest_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|not_provided": 1,
    "Type_2_collagenopathy|not_provided|Stickler_syndrome_type_1": 1,
    "not_provided|Achondrogenesis_type_II|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Namaqualand_hip_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_congenita|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloperipheral_dysplasia": 1,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_specified|not_provided|Type_2_collagenopathy|Achondrogenesis_type_II|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Kniest_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia_congenita|Hypochondrogenesis|Spondyloepimetaphyseal_dysplasia|_Strudwick_type": 1,
    "not_provided|COL2A1-related_disorder|not_specified": 1,
    "Stickler_syndrome|_type_I|_nonsyndromic_ocular|Stickler_syndrome_type_1|not_provided|Type_II_Collagenopathies": 1,
    "not_provided|COL2A1-related_disorder|Stickler_syndrome_type_1": 1,
    "Achondrogenesis_type_II|Stickler_syndrome_type_1|not_provided": 1,
    "Platyspondylic_dysplasia|_Torrance_type|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome_type_1|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloperipheral_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_congenita|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Kniest_dysplasia|Achondrogenesis_type_II|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Multiple_epiphyseal_dysplasia|_Beighton_type|Platyspondylic_dysplasia|_Torrance_type|Namaqualand_hip_dysplasia": 1,
    "Avascular_necrosis_of_femoral_head|_primary|_1": 3,
    "Spondyloepiphyseal_dysplasia|_Namaqualand_type": 1,
    "Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_congenita|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Legg-Calve-Perthes_disease|Kniest_dysplasia|not_provided": 1,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Stickler_syndrome_type_1|Myopia|not_provided": 1,
    "Type_II_Collagenopathies|COL2A1-related_disorder|Stickler_syndrome_type_1|not_provided": 1,
    "Type_II_Collagenopathies|not_provided|Stickler_syndrome_type_1|Connective_tissue_disorder|not_specified": 1,
    "not_provided|Stickler_syndrome|_type_I|_nonsyndromic_ocular": 4,
    "not_provided|Stickler_syndrome_type_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular": 1,
    "Retinal_dystrophy|not_provided|Kniest_dysplasia|Legg-Calve-Perthes_disease|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Achondrogenesis_type_II|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Inborn_genetic_diseases": 1,
    "not_provided|Connective_tissue_disorder|Type_II_Collagenopathies|not_specified|Stickler_syndrome_type_1": 1,
    "not_provided|COL2A1-related_disorder|Inborn_genetic_diseases": 3,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Epiphyseal_dysplasia|_multiple|_6|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Namaqualand_hip_dysplasia|Spondylometaphyseal_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Stickler_syndrome|_type_4|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Achondrogenesis_type_II": 1,
    "not_provided|Platyspondylic_dysplasia|_Torrance_type": 1,
    "Spondylometaphyseal_dysplasia|_Schmidt_type": 1,
    "Type_2_collagenopathy|Spondyloperipheral_dysplasia": 1,
    "Stickler_syndrome_type_1|not_specified|not_provided|Type_II_Collagenopathies": 1,
    "COL2A1-related_disorder|not_provided|not_specified": 3,
    "Stickler_syndrome_type_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular|not_provided": 1,
    "COL2A1-related_disorder|Connective_tissue_disorder|Achondrogenesis_type_II|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Namaqualand_hip_dysplasia|Kniest_dysplasia|Legg-Calve-Perthes_disease|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloperipheral_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome_type_1|Multiple_epiphyseal_dysplasia|_Beighton_type|not_specified|not_provided|Type_II_Collagenopathies": 1,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Platyspondylic_dysplasia|_Torrance_type|Kniest_dysplasia|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Namaqualand_hip_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Achondrogenesis_type_II|not_provided": 1,
    "Connective_tissue_disorder|Stickler_syndrome_type_1|not_provided": 1,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1|not_provided|not_specified": 1,
    "Spondyloepiphyseal_dysplasia|_Stanescu_type|not_provided|Type_2_collagenopathy": 1,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1|COL2A1-related_disorder|not_provided": 1,
    "Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Namaqualand_hip_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloperipheral_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Stickler_syndrome_type_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Connective_tissue_disorder|not_provided|not_specified": 1,
    "not_provided|Namaqualand_hip_dysplasia": 1,
    "Stickler_syndrome_type_1|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_congenita|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Achondrogenesis_type_II|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Kniest_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Namaqualand_hip_dysplasia|Multiple_epiphyseal_dysplasia|_Beighton_type": 1,
    "COL2A1-related_disorder|Achondrogenesis_type_II": 1,
    "Stickler_syndrome_type_1|Achondrogenesis_type_II|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloperipheral_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia|_Stanescu_type|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|not_provided|Connective_tissue_disorder|not_specified|Type_II_Collagenopathies": 1,
    "not_provided|not_specified|Type_II_Collagenopathies|Stickler_syndrome_type_1": 1,
    "not_provided|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome_type_1": 1,
    "Stickler_syndrome_type_1|not_specified|Type_II_Collagenopathies|not_provided": 1,
    "COL2A1-related_disorder|Connective_tissue_disorder|not_provided|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Stickler_syndrome_type_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular": 1,
    "Spondyloepimetaphyseal_dysplasia|_Strudwick_type|not_provided": 1,
    "COL2A1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Stickler_syndrome_type_1": 1,
    "not_specified|COL2A1-related_disorder|not_provided": 2,
    "Stickler_syndrome_type_1|Avascular_necrosis_of_femoral_head|_primary|_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondylometaphyseal_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Namaqualand_hip_dysplasia|Kniest_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|Legg-Calve-Perthes_disease|Multiple_epiphyseal_dysplasia|_Beighton_type|Platyspondylic_dysplasia|_Torrance_type|Spondyloperipheral_dysplasia|Achondrogenesis_type_II|Stickler_syndrome|Inborn_genetic_diseases|not_provided|Autosomal_dominant_rhegmatogenous_retinal_detachment": 1,
    "COL2A1-related_skeletal_dysplasia|not_specified": 1,
    "not_provided|Developmental_dysplasia_of_the_hip|Multiple_epiphyseal_dysplasia|Hypoplastic_acetabulae|Scoliosis|Short_stature|Hearing_impairment": 1,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1|not_specified|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Achondrogenesis_type_II|Spondyloperipheral_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Connective_tissue_disorder|not_provided": 2,
    "Avascular_necrosis_of_femoral_head|_primary|_1|Connective_tissue_disorder": 1,
    "not_provided|Achondrogenesis_type_II|Spondyloperipheral_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Legg-Calve-Perthes_disease|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Kniest_dysplasia|Multiple_epiphyseal_dysplasia|_Beighton_type|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type": 1,
    "not_provided|Retinal_dystrophy|Stickler_syndrome_type_1": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Achondrogenesis_type_II|Avascular_necrosis_of_femoral_head|_primary|_1|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Namaqualand_hip_dysplasia|Legg-Calve-Perthes_disease|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|not_provided|Inborn_genetic_diseases": 1,
    "Spondylometaphyseal_dysplasia|not_provided": 1,
    "not_provided|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Stickler_syndrome_type_1|COL2A1-related_disorder|Achondrogenesis_type_II|Retinal_dystrophy": 1,
    "Type_II_Collagenopathies|COL2A1-related_disorder|Stickler_syndrome_type_1": 1,
    "COL2A1-related_disorder|not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 1,
    "not_provided|Kniest_dysplasia": 2,
    "Inborn_genetic_diseases|not_provided|Achondrogenesis_type_II|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Stickler_syndrome_type_1|Kniest_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Hypochondrogenesis": 1,
    "not_specified|Orofacial_cleft_1|Stickler_syndrome_type_1|not_provided": 1,
    "not_provided|Achondrogenesis_type_II|Inborn_genetic_diseases": 1,
    "Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloperipheral_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome_type_1|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Platyspondylic_dysplasia|_Torrance_type|Namaqualand_hip_dysplasia|Achondrogenesis_type_II|not_provided": 1,
    "Connective_tissue_disorder|Stickler_syndrome_type_1|not_provided|Micrognathia|Heart|_malformation_of|See_cases": 1,
    "Kniest_dysplasia|not_provided": 2,
    "Kniest_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Spondyloperipheral_dysplasia|Platyspondylic_dysplasia|_Torrance_type": 1,
    "Inborn_genetic_diseases|Stickler_syndrome|_type_I|_nonsyndromic_ocular": 1,
    "not_provided|See_cases|Spondyloepiphyseal_dysplasia|_Stanescu_type": 1,
    "Stargardt_disease|Stickler_syndrome_type_1|not_provided": 1,
    "not_provided|Spondyloepiphyseal_dysplasia_congenita|Stickler_syndrome_type_1": 1,
    "Spondyloepimetaphyseal_dysplasia|_Strudwick_type|not_provided|Stickler_syndrome_type_1": 1,
    "Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Kniest_dysplasia|COL2A1-related_disorder": 1,
    "Kniest_dysplasia|Stickler_syndrome_type_1|not_provided": 1,
    "Type_II_Collagenopathies|not_specified|Stickler_syndrome_type_1|not_provided": 1,
    "Stickler_syndrome_type_1|Type_II_Collagenopathies|not_provided|Connective_tissue_disorder": 2,
    "Hearing_impairment|not_specified|COL2A1-related_disorder|not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 1,
    "Stickler_syndrome_type_1|not_provided|Connective_tissue_disorder|Type_II_Collagenopathies|not_specified": 1,
    "not_provided|Type_II_Collagenopathies|not_specified|Stickler_syndrome_type_1|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Avascular_necrosis_of_femoral_head|_primary|_1|Achondrogenesis_type_II|Spondyloperipheral_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Connective_tissue_disorder": 1,
    "Retinal_dystrophy|not_provided|COL2A1-related_disorder": 1,
    "Stickler_syndrome_type_1|Connective_tissue_disorder|Type_II_Collagenopathies|not_specified|not_provided": 1,
    "COL2A1-related_phenotype": 1,
    "Spondyloepiphyseal_dysplasia_congenita|not_provided|Stickler_syndrome_type_1": 1,
    "Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Achondrogenesis_type_II|Namaqualand_hip_dysplasia|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|not_provided": 1,
    "Stickler_syndrome_type_1|not_provided|not_specified|Type_II_Collagenopathies": 1,
    "COL2A1-related_disorder|not_provided|Achondrogenesis_type_II|Avascular_necrosis_of_femoral_head|_primary|_1|Stickler_syndrome_type_1|Spondyloperipheral_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepiphyseal_dysplasia|_Stanescu_type|Multiple_epiphyseal_dysplasia|_Beighton_type|Namaqualand_hip_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita": 1,
    "Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Kniest_dysplasia|not_provided": 1,
    "Stickler_syndrome|_type_I|_nonsyndromic_ocular|not_provided": 3,
    "Spondylometaphyseal_dysplasia_-_Sutcliffe_type|not_provided": 1,
    "Kniest_dysplasia|Multiple_epiphyseal_dysplasia|_Beighton_type": 1,
    "Type_II_Collagenopathies|COL2A1-related_disorder|Stickler_Syndrome|_Dominant|not_provided": 1,
    "Spondyloepiphyseal_dysplasia|_Stanescu_type|not_specified|not_provided": 1,
    "not_provided|COL2A1-related_disorder|Connective_tissue_disorder": 1,
    "not_provided|Autosomal_dominant_rhegmatogenous_retinal_detachment": 1,
    "Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Type_II_Collagenopathies|Multiple_epiphyseal_dysplasia|_Beighton_type|Legg-Calve-Perthes_disease|Platyspondylic_dysplasia|_Torrance_type|Achondrogenesis_type_II|Spondyloepiphyseal_dysplasia|_Stanescu_type|Kniest_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Namaqualand_hip_dysplasia|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|not_provided|Abnormality_of_the_skeletal_system": 1,
    "Achondrogenesis_type_II|Multiple_epiphyseal_dysplasia|_Beighton_type|Kniest_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Namaqualand_hip_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloperipheral_dysplasia|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Stickler_syndrome_type_1|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|not_provided|not_specified": 1,
    "Retinal_detachment": 2,
    "Acetabular_dysplasia|not_provided|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Achondrogenesis_type_II|Stickler_syndrome_type_1": 1,
    "Stickler_syndrome_type_1|not_provided|Multiple_epiphyseal_dysplasia|_Beighton_type|Legg-Calve-Perthes_disease|Kniest_dysplasia|Namaqualand_hip_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondylometaphyseal_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloperipheral_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Achondrogenesis_type_II|COL2A1-related_disorder|Type_II_Collagenopathies": 1,
    "not_provided|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloperipheral_dysplasia|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia|_Stanescu_type|Stickler_syndrome_type_1|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Avascular_necrosis_of_femoral_head|_primary|_1|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Platyspondylic_dysplasia|_Torrance_type|Namaqualand_hip_dysplasia|Achondrogenesis_type_II": 1,
    "not_specified|Stickler_syndrome_type_1|Type_II_Collagenopathies|not_provided": 1,
    "Type_II_Collagenopathies|not_provided|not_specified|Stickler_syndrome_type_1": 1,
    "Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|not_provided": 1,
    "Stickler_syndrome_type_1|Type_II_Collagenopathies|not_provided|Connective_tissue_disorder|not_specified": 1,
    "COL2A1-related_disorder|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|COL2A1-related_disorder": 1,
    "not_provided|Connective_tissue_disorder|Type_II_Collagenopathies|Stickler_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Stickler_syndrome_type_1|Type_II_Collagenopathies": 1,
    "not_specified|not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 2,
    "Stickler_syndrome_type_1|not_provided|Type_II_Collagenopathies|not_specified": 1,
    "Stickler_syndrome_type_1|Achondrogenesis_type_II|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Spondyloperipheral_dysplasia": 1,
    "Type_II_Collagenopathies|Stickler_syndrome_type_1|not_specified|not_provided|Connective_tissue_disorder": 1,
    "COL2A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Multiple_epiphyseal_dysplasia|_Beighton_type|Legg-Calve-Perthes_disease|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Kniest_dysplasia|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloepiphyseal_dysplasia_congenita|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Avascular_necrosis_of_femoral_head|_primary|_1|Namaqualand_hip_dysplasia|Spondylometaphyseal_dysplasia_-_Sutcliffe_type|Achondrogenesis_type_II": 1,
    "Stickler_syndrome_type_1|COL2A1-related_disorder": 1,
    "not_provided|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Avascular_necrosis_of_femoral_head|_primary|_1|Spondyloepiphyseal_dysplasia|_Stanescu_type|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Platyspondylic_dysplasia|_Torrance_type|Kniest_dysplasia|Achondrogenesis_type_II|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Legg-Calve-Perthes_disease|Namaqualand_hip_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondylometaphyseal_dysplasia": 1,
    "COL2A1-related_disorder|not_provided|Stickler_syndrome_type_1|Type_II_Collagenopathies": 1,
    "Connective_tissue_disorder|COL2A1-related_disorder|not_specified|not_provided|Type_II_Collagenopathies|Stickler_syndrome_type_1": 1,
    "Stickler_syndrome_type_1|not_provided|Stickler_syndrome|_type_I|_nonsyndromic_ocular|COL2A1-related_disorder": 1,
    "not_specified|Intellectual_disability|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|COL2A1-related_disorder|Stickler_syndrome_type_1": 1,
    "not_provided|Stickler_syndrome_type_1|not_specified|Connective_tissue_disorder|Type_II_Collagenopathies": 1,
    "Achondrogenesis_type_II|Avascular_necrosis_of_femoral_head|_primary|_1|Legg-Calve-Perthes_disease|Kniest_dysplasia|Spondyloepiphyseal_dysplasia_with_metatarsal_shortening|Spondyloepimetaphyseal_dysplasia|_Strudwick_type|Vitreoretinopathy_with_phalangeal_epiphyseal_dysplasia|Spondyloepiphyseal_dysplasia_congenita|Spondyloperipheral_dysplasia|Stickler_syndrome_type_1|Multiple_epiphyseal_dysplasia|_Beighton_type|Spondyloepiphyseal_dysplasia|_Stanescu_type|Namaqualand_hip_dysplasia|Platyspondylic_dysplasia|_Torrance_type|Stickler_syndrome|_type_I|_nonsyndromic_ocular|not_provided": 1,
    "Type_II_Collagenopathies|Stickler_Syndrome|_Dominant|not_provided": 1,
    "Glycogen_storage_disease|_type_VII": 819,
    "not_provided|Glycogen_storage_disease|_type_VII": 25,
    "PFKM-related_disorder": 7,
    "Glycogen_storage_disease|_type_VII|not_provided": 14,
    "PFKM-related_disorder|not_provided|Glycogen_storage_disease|_type_VII": 2,
    "not_provided|Glycogen_storage_disease|_type_VII|Inborn_genetic_diseases": 2,
    "Glycogen_storage_disease|_type_VII|Inborn_genetic_diseases": 8,
    "not_specified|Glycogen_storage_disease|_type_VII": 8,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_VII": 10,
    "Rhabdomyolysis|not_provided|Glycogen_storage_disease|_type_VII": 1,
    "Peroxisomal_biogenesis_disorder_3b": 3,
    "Glycogen_storage_disease|_type_VII|not_specified|not_provided": 2,
    "Glycogen_storage_disease|_type_VII|Inborn_genetic_diseases|not_provided": 2,
    "Glycogen_storage_disease|_type_VII|PFKM-related_disorder": 6,
    "not_provided|Glycogen_storage_disease|_type_VII|not_specified": 4,
    "Glycogen_storage_disease|_type_VII|not_specified": 7,
    "PFKM-related_disorder|Glycogen_storage_disease|_type_VII|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease|_type_VII": 4,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_VII|not_provided": 2,
    "PFKM-related_disorder|Glycogen_storage_disease|_type_VII": 3,
    "PFKM-related_disorder|not_specified|Glycogen_storage_disease|_type_VII": 1,
    "not_provided|not_specified|Glycogen_storage_disease|_type_VII": 2,
    "Inborn_genetic_diseases|not_provided|PFKM-related_disorder|Glycogen_storage_disease|_type_VII": 1,
    "not_specified|Glycogen_storage_disease|_type_VII|not_provided": 3,
    "Glycogen_storage_disease|Glycogen_storage_disease|_type_VII|not_provided": 1,
    "not_specified|not_provided|Glycogen_storage_disease|_type_VII": 1,
    "Lethal_congenital_contracture_syndrome_8": 6,
    "ADCY6-related_disorder": 11,
    "ADCY6-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|Lethal_congenital_contracture_syndrome_8": 1,
    "Lethal_congenital_contracture_syndrome_8|Inborn_genetic_diseases": 1,
    "DDX23-related_disorder": 1,
    "not_provided|Failure_to_thrive|Fetal_growth_restriction|Abnormal_facial_shape|Motor_delay": 1,
    "DDX23-related_Neurodevelopmental_disorder|not_provided": 1,
    "Inborn_genetic_diseases|DDX23-related_disorder": 1,
    "Primary_ciliary_dyskinesia_27": 155,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_27": 9,
    "Primary_ciliary_dyskinesia_27|CCDC65-related_disorder": 1,
    "Primary_ciliary_dyskinesia_27|not_provided": 8,
    "CCDC65-related_disorder|Primary_ciliary_dyskinesia_27|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_27": 1,
    "Primary_ciliary_dyskinesia_27|Inborn_genetic_diseases": 7,
    "Primary_ciliary_dyskinesia_27|not_specified|not_provided": 4,
    "CCDC65-related_disorder": 2,
    "not_provided|Primary_ciliary_dyskinesia_27": 7,
    "not_provided|Primary_ciliary_dyskinesia_27|not_specified": 3,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_27|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_27|not_provided": 1,
    "CCDC65-related_disorder|Primary_ciliary_dyskinesia_27": 2,
    "Microcephaly|Intellectual_disability|Atrophy/Degeneration_affecting_the_central_nervous_system|Heart|_malformation_of|Seizure|Hypotonia|Scoliosis": 1,
    "See_cases|Global_developmental_delay|Hypotonia|Myopathic_facies|not_provided|Bifid_uvula|Autism|Abnormality_of_the_dentition|Delayed_early-childhood_social_milestone_development|Neurodevelopmental_delay|Clinodactyly|Long_ear|Delayed_speech_and_language_development|Motor_delay|Self-injurious_behavior|Long_neck|Intellectual_disability|Pectus_excavatum|Microcephaly|Atrophy/Degeneration_affecting_the_central_nervous_system": 1,
    "Intellectual_disability|Atrophy/Degeneration_affecting_the_central_nervous_system|Microcephaly|Dystonic_disorder|Scoliosis": 2,
    "Intellectual_disability|Atrophy/Degeneration_affecting_the_central_nervous_system|Seizure|not_provided": 1,
    "Intellectual_disability|Kyphosis|Atrophy/Degeneration_affecting_the_central_nervous_system": 1,
    "Tooth_agenesis|_selective|_8|not_specified|not_provided|Split_hand-foot_malformation_6": 1,
    "not_provided|Split_hand-foot_malformation_6": 3,
    "Split_hand-foot_malformation_6": 15,
    "not_specified|not_provided|WNT10B-related_disorder": 1,
    "Tooth_agenesis|_selective|_8|Split_hand-foot_malformation_6": 1,
    "WNT10B-related_disorder": 4,
    "Tooth_agenesis|_selective|_8": 2,
    "WNT10B-related_disorder|Split_hand-foot_malformation_6": 1,
    "Split_hand-foot_malformation_6|not_provided": 1,
    "WNT1-related_disorder": 3,
    "WNT1-related_disorder|not_provided": 2,
    "OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO|Osteogenesis_imperfecta_type_15|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|WNT1-related_disorder": 1,
    "OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO|Osteogenesis_imperfecta_type_15": 2,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_15|OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO": 1,
    "not_provided|Osteogenesis_imperfecta_type_15": 3,
    "not_provided|Osteogenesis_imperfecta_type_15|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|WNT1-related_disorder|Osteogenesis_imperfecta_type_15|OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO|not_provided|Inborn_genetic_diseases": 1,
    "Osteogenesis_imperfecta_type_15|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Osteogenesis_imperfecta|not_provided": 1,
    "OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO": 2,
    "Osteogenesis_imperfecta_type_15|OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Osteogenesis_imperfecta_type_15|OSTEOPOROSIS|_EARLY-ONSET|_SUSCEPTIBILITY_TO|Inborn_genetic_diseases": 1,
    "Keratoconus|Osteogenesis_imperfecta_type_15": 1,
    "Kabuki_syndrome": 3107,
    "Kabuki_syndrome|not_specified|not_provided": 23,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 13,
    "Kabuki_syndrome|Neurodevelopmental_disorder": 1,
    "not_provided|Kabuki_syndrome|not_specified": 9,
    "Kabuki_syndrome|not_provided": 162,
    "KMT2D-related_disorder": 174,
    "not_provided|Kabuki_syndrome_1|Kabuki_syndrome": 3,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome": 37,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome_1": 3,
    "Kabuki_syndrome_1|Seizure": 1,
    "Kabuki_syndrome|not_provided|not_specified": 14,
    "Kabuki_syndrome|Inborn_genetic_diseases": 42,
    "not_specified|not_provided|Kabuki_syndrome|Kabuki_syndrome_1": 2,
    "Kabuki_syndrome|Kabuki_syndrome_1": 43,
    "Kabuki_syndrome|not_provided|Kabuki_syndrome_1": 13,
    "Kabuki_syndrome_1|Kabuki_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "KMT2D-related_disorder|Kabuki_syndrome": 167,
    "Kabuki_syndrome_1|Kabuki_syndrome": 45,
    "Kabuki_syndrome|not_provided|KMT2D-related_disorder": 15,
    "not_provided|Branchial_cleft_anomaly|KMT2D-related_disorder|Kabuki_syndrome|Kabuki_syndrome_1|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Kabuki_syndrome": 3,
    "Kabuki_syndrome|not_specified": 43,
    "not_specified|Kabuki_syndrome|not_provided": 12,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 192,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 11,
    "not_provided|KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome": 2,
    "not_specified|Kabuki_syndrome|KMT2D-related_disorder": 2,
    "not_provided|Kabuki_syndrome|KMT2D-related_disorder": 17,
    "Kabuki_syndrome_1|not_provided|Kabuki_syndrome": 9,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Inborn_genetic_diseases|Kabuki_syndrome|not_provided": 1,
    "not_provided|Kabuki_syndrome": 121,
    "not_specified|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome": 57,
    "Kabuki_syndrome|KMT2D-related_disorder": 71,
    "KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome|not_specified|not_provided|Kabuki_syndrome_1": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|not_provided": 10,
    "not_provided|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 5,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|Kabuki_syndrome": 12,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 87,
    "Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "Vein_of_Galen_aneurysmal_malformation|Kabuki_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_provided|Kabuki_syndrome": 5,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_provided|Kabuki_syndrome_1": 4,
    "Kabuki_syndrome|Kabuki_syndrome_1|not_specified|not_provided": 3,
    "Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 38,
    "not_provided|not_specified|KMT2D-related_disorder|Kabuki_syndrome|Kabuki_syndrome_1": 2,
    "not_specified|not_provided|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_provided": 8,
    "Kabuki_syndrome_1|KMT2D-related_disorder|Kabuki_syndrome|not_provided": 2,
    "KMT2D-related_disorder|not_provided": 11,
    "not_specified|Kabuki_syndrome": 32,
    "Kabuki_syndrome_1|not_provided": 22,
    "KMT2D-related_disorder|Kabuki_syndrome|not_provided|not_specified": 6,
    "Kabuki_syndrome|Kabuki_syndrome_1|not_provided": 10,
    "not_specified|Kabuki_syndrome|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|not_provided": 6,
    "not_provided|Kabuki_syndrome|KMT2D-related_disorder|Kabuki_syndrome_1": 1,
    "not_specified|not_provided|Kabuki_syndrome": 17,
    "KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome|not_specified|Kabuki_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "not_provided|KMT2D-related_disorder": 9,
    "not_specified|Kabuki_syndrome|not_provided|KMT2D-related_disorder": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases|Kabuki_syndrome": 4,
    "Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 21,
    "Kabuki_syndrome_1|not_provided|KMT2D-related_disorder|Kabuki_syndrome": 1,
    "Inborn_genetic_diseases|KMT2D-related_disorder|Kabuki_syndrome|Kabuki_syndrome_1": 2,
    "not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome": 4,
    "KMT2D-related_disorder|Kabuki_syndrome|Kabuki_syndrome_1": 6,
    "not_provided|Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 5,
    "KMT2D-related_disorder|Kabuki_syndrome_1|not_provided|Kabuki_syndrome": 1,
    "Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|not_provided": 3,
    "Kabuki_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder": 3,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "not_provided|KMT2D-related_disorder|Kabuki_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|KMT2D-related_disorder|not_provided|Kabuki_syndrome": 2,
    "Kabuki_syndrome|KMT2D-related_disorder|not_provided": 21,
    "KMT2D-related_disorder|Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 3,
    "Intellectual_disability|Kabuki_syndrome_1": 1,
    "not_provided|KMT2D-related_disorder|Kabuki_syndrome": 18,
    "KMT2D-related_disorder|Kabuki_syndrome|not_provided": 39,
    "Kabuki_syndrome_1|not_specified|Kabuki_syndrome|not_provided": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Kabuki_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 3,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|KMT2D-related_disorder|not_provided": 4,
    "Kabuki_syndrome|not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 2,
    "Kabuki_syndrome|See_cases": 2,
    "not_provided|Kabuki_syndrome|Kabuki_syndrome_1": 7,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_specified": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome": 17,
    "KMT2D-related_disorder|Kabuki_syndrome|not_specified": 3,
    "Kabuki_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_specified": 3,
    "Kabuki_syndrome|KMT2D-related_disorder|not_specified": 2,
    "Kabuki_syndrome_1|not_specified|not_provided|Kabuki_syndrome": 2,
    "Kabuki_syndrome|KMT2D-related_disorder|not_specified|not_provided": 5,
    "not_specified|KMT2D-related_disorder|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_specified|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "KMT2D-related_disorder|not_specified|Kabuki_syndrome": 4,
    "not_specified|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 1,
    "Kabuki_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder|not_provided": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder|Kabuki_syndrome": 3,
    "Kabuki_syndrome|Inborn_genetic_diseases|Kabuki_syndrome_1": 3,
    "Inborn_genetic_diseases|KMT2D-related_disorder|Kabuki_syndrome|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder|Kabuki_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|not_provided|Kabuki_syndrome": 2,
    "not_specified|KMT2D-related_disorder|Kabuki_syndrome": 4,
    "Inborn_genetic_diseases|not_specified|Kabuki_syndrome": 3,
    "Inborn_genetic_diseases|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 2,
    "not_provided|Kabuki_syndrome|Inborn_genetic_diseases": 4,
    "not_specified|Kabuki_syndrome|not_provided|Kabuki_syndrome_1": 3,
    "KMT2D-related_disorder|Inborn_genetic_diseases": 4,
    "not_specified|Kabuki_syndrome|KMT2D-related_disorder|not_provided": 2,
    "Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_provided": 3,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_specified|not_provided|Kabuki_syndrome_1": 2,
    "Kabuki_syndrome|KMT2D-related_disorder|not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 1,
    "Inborn_genetic_diseases|KMT2D-related_disorder|Kabuki_syndrome|not_provided|Kabuki_syndrome_1": 1,
    "Kabuki_syndrome|not_specified|not_provided|Kabuki_syndrome_1": 10,
    "KMT2D-related_disorder|Kabuki_syndrome_1|Kabuki_syndrome": 3,
    "KMT2D-related_disorder|Multiple_myeloma|Kabuki_syndrome_1|not_provided|Kabuki_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases": 4,
    "Kabuki_syndrome_1|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_provided": 5,
    "Kabuki_syndrome|KMT2D-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Kabuki_syndrome_1|KMT2D-related_disorder|Kabuki_syndrome": 2,
    "Kabuki_syndrome|not_specified|KMT2D-related_disorder|Dystonia|_early-onset|_and/or_spastic_paraplegia": 1,
    "KMT2D-related_disorder|not_specified|Kabuki_syndrome|Kabuki_syndrome_1": 1,
    "Kabuki_syndrome|not_provided|KMT2D-related_disorder|not_specified": 2,
    "Kabuki_syndrome|not_provided|Kabuki_syndrome_1|not_specified": 2,
    "Kabuki_syndrome_1|not_provided|KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Branchial_cleft_anomaly|not_provided": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome_1|Kabuki_syndrome|not_specified": 1,
    "Kabuki_syndrome|Inborn_genetic_diseases|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 4,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|not_specified|not_provided": 1,
    "Dandy-Walker_syndrome|Kabuki_syndrome_1": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 1,
    "not_provided|not_specified|KMT2D-related_disorder|Kabuki_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Kabuki_syndrome|Kabuki_syndrome_1": 1,
    "not_specified|KMT2D-related_disorder|Kabuki_syndrome|not_provided": 1,
    "not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "Kabuki_syndrome|Inborn_genetic_diseases|KMT2D-related_disorder": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|Kabuki_syndrome_1": 2,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome|not_provided": 7,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|not_provided|KMT2D-related_disorder": 1,
    "not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Kabuki_syndrome": 9,
    "Eccrine_porocarcinoma|Kabuki_syndrome": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome|not_specified|Kabuki_syndrome_1": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 1,
    "Kabuki_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Kabuki_syndrome_1|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "Branchial_cleft_anomaly|Kabuki_syndrome_1": 2,
    "not_provided|Kabuki_syndrome|KMT2D-related_disorder|not_specified|Left_ventricular_noncompaction": 1,
    "not_specified|Kabuki_syndrome_1|not_provided|Kabuki_syndrome": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|not_provided|KMT2D-related_disorder": 1,
    "Intellectual_disability|not_specified|Kabuki_syndrome": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Kabuki_syndrome": 1,
    "Intellectual_disability|not_provided|Kabuki_syndrome": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_provided|not_specified|Kabuki_syndrome_1": 1,
    "KMT2D-related_disorder|Kabuki_syndrome|not_provided|Kabuki_syndrome_1": 5,
    "Intellectual_disability|Kabuki_syndrome": 2,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|Kabuki_syndrome|not_specified": 1,
    "Kabuki_syndrome|not_specified|Kabuki_syndrome_1": 2,
    "Kabuki_syndrome_1|not_provided|Kabuki_syndrome|not_specified": 1,
    "Kabuki_syndrome|not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 5,
    "KMT2D-related_disorder|Kabuki_syndrome|Inborn_genetic_diseases": 3,
    "Kabuki_syndrome|not_specified|Kabuki_syndrome_1|not_provided": 1,
    "KMT2D-related_disorder|not_specified|Kabuki_syndrome|not_provided": 5,
    "not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 1,
    "Kabuki_syndrome_1|Lymphoma": 1,
    "Stenosis_of_the_external_auditory_canal|Strabismus|Amblyopia|Microtia|Choanal_atresia|Abnormal_pinna_morphology|Kabuki_syndrome_1": 1,
    "Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_provided": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_provided|KMT2D-related_disorder": 1,
    "Branchial_cleft_anomaly|Kabuki_syndrome": 1,
    "Kabuki_syndrome|Inborn_genetic_diseases|Kabuki_syndrome_1|not_provided": 1,
    "not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 2,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder|Kabuki_syndrome|not_provided": 2,
    "Kabuki_syndrome|not_specified|not_provided|KMT2D-related_disorder": 1,
    "KMT2D-related_disorder|Kabuki_syndrome_1|Kabuki_syndrome|not_provided": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|Kabuki_syndrome_1|not_provided": 1,
    "Kabuki_syndrome|not_provided|KMT2D-related_disorder|Kabuki_syndrome_1|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "KMT2D-related_disorder|Kabuki_syndrome|not_specified|not_provided": 4,
    "Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder": 3,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_provided|Kabuki_syndrome": 4,
    "Inborn_genetic_diseases|Kabuki_syndrome|Kabuki_syndrome_1": 4,
    "Kabuki_syndrome_1|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome": 5,
    "Inborn_genetic_diseases|not_specified|not_provided|KMT2D-related_disorder|Kabuki_syndrome": 1,
    "not_provided|Kabuki_syndrome_1|CHARGE_syndrome": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "KMT2D-related_disorder|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome": 2,
    "KMT2D-related_disorder|not_provided|not_specified|Kabuki_syndrome|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome|not_provided|KMT2D-related_disorder|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome|not_specified|KMT2D-related_disorder|Inborn_genetic_diseases": 1,
    "KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome|not_provided": 1,
    "Kabuki_syndrome|Kabuki_syndrome_1|not_provided|not_specified": 3,
    "Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder": 2,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|Inborn_genetic_diseases": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome|Inborn_genetic_diseases": 2,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases|Kabuki_syndrome|VISS_syndrome": 1,
    "not_provided|KMT2D-related_disorder|Kabuki_syndrome_1": 1,
    "not_provided|Kabuki_syndrome|not_specified|Kabuki_syndrome_1": 1,
    "Inborn_genetic_diseases|KMT2D-related_disorder|Kabuki_syndrome": 5,
    "not_provided|not_specified|Kabuki_syndrome_1|Inborn_genetic_diseases|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "Inborn_genetic_diseases|KMT2D-related_disorder|not_specified|Kabuki_syndrome|not_provided|Kabuki_syndrome_1": 1,
    "not_provided|Kabuki_syndrome_1|KMT2D-related_disorder": 2,
    "KMT2D-related_disorder|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome|not_specified|not_provided": 1,
    "not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder": 1,
    "Kabuki_syndrome_1|not_specified|not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 1,
    "not_provided|KMT2D-related_disorder|Kabuki_syndrome|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|Kabuki_syndrome|Kabuki_syndrome_1|not_specified": 1,
    "Kabuki_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "Kabuki_syndrome|not_specified|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 1,
    "KMT2D-related_disorder|Kabuki_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Kabuki_syndrome|not_specified|KMT2D-related_disorder": 1,
    "KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Kabuki_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 2,
    "KMT2D-related_disorder|Kabuki_syndrome|Inborn_genetic_diseases|not_provided|Kabuki_syndrome_1": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome|not_specified": 1,
    "Microcephaly|Kabuki_syndrome_1|not_provided|Kabuki_syndrome": 1,
    "not_specified|not_provided|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 1,
    "not_provided|Kabuki_syndrome|Kabuki_syndrome_1|not_specified": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|Inborn_genetic_diseases": 4,
    "not_specified|Kabuki_syndrome_1|not_provided|KMT2D-related_disorder|Kabuki_syndrome": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_provided": 4,
    "KMT2D-related_disorder|Kabuki_syndrome|not_provided|not_specified|Kabuki_syndrome_1": 2,
    "KMT2D-related_disorder|not_specified|not_provided|Kabuki_syndrome_1|Kabuki_syndrome": 4,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "KMT2D-related_disorder|not_provided|not_specified|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder": 3,
    "Kabuki_syndrome|not_specified|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|not_provided|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "not_specified|KMT2D-related_disorder|Kabuki_syndrome_1|Kabuki_syndrome|not_provided": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome|not_specified": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_specified|not_provided|Intellectual_disability": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome_1|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Kabuki_syndrome|KMT2D-related_disorder|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 1,
    "KMT2D-related_disorder|not_provided|Kabuki_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_provided|not_specified": 1,
    "KMT2D-related_disorder|Inborn_genetic_diseases|not_specified|Kabuki_syndrome|not_provided": 1,
    "Kabuki_syndrome_1|not_provided|not_specified": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|KMT2D-related_disorder|not_provided": 1,
    "KMT2D-related_disorder|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome": 2,
    "KMT2D-related_disorder|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_provided": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_1|not_provided|Kabuki_syndrome|KMT2D-related_disorder": 1,
    "Kabuki_syndrome_1|Inborn_genetic_diseases|KMT2D-related_disorder|not_provided": 1,
    "not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|not_provided|not_specified": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome_1|not_provided": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder": 3,
    "Inborn_genetic_diseases|KMT2D-related_disorder": 1,
    "not_provided|KMT2D-related_disorder|Kabuki_syndrome|Kabuki_syndrome_1": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome_1": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Kabuki_syndrome|not_specified|not_provided": 1,
    "Lung_cancer|Kabuki_syndrome_1": 1,
    "Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|not_provided|Kabuki_syndrome_1|KMT2D-related_disorder|not_specified": 1,
    "KMT2D-related_disorder|Kabuki_syndrome_1": 2,
    "not_specified|Inborn_genetic_diseases|Kabuki_syndrome|not_provided": 1,
    "not_provided|Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder": 1,
    "Connective_tissue_nevi|Seizure": 1,
    "not_provided|KMT2D-related_disorder|not_specified|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "KMT2D-related_disorder|Kabuki_syndrome|not_provided|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|not_provided|KMT2D-related_disorder": 1,
    "not_provided|Kabuki_syndrome_1|KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome": 1,
    "not_provided|Kabuki_syndrome|Inborn_genetic_diseases|KMT2D-related_disorder": 1,
    "Kabuki_syndrome_1|KMT2D-related_disorder|Kabuki_syndrome": 1,
    "KMT2D-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|not_specified|not_provided": 1,
    "not_provided|Kabuki_syndrome|KMT2D-related_disorder|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "not_provided|not_specified|Kabuki_syndrome_1": 1,
    "Kabuki_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Kabuki_syndrome": 1,
    "not_provided|KMT2D-related_disorder|not_specified|Kabuki_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|KMT2D-related_disorder|Kabuki_syndrome": 1,
    "not_provided|Kabuki_syndrome|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_specified": 1,
    "Kabuki_syndrome|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_provided|KMT2D-related_disorder": 1,
    "KMT2D-related_disorder|not_specified|not_provided|Kabuki_syndrome": 3,
    "Kabuki_syndrome|not_specified|KMT2D-related_disorder|not_provided": 1,
    "KMT2D-related_disorder|not_specified": 1,
    "Intellectual_disability|Kabuki_syndrome_1|Kabuki_syndrome": 1,
    "not_specified|Kabuki_syndrome_1": 1,
    "not_provided|Kabuki_syndrome|KMT2D-related_disorder|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1": 1,
    "KMT2D-related_disorder|not_provided|not_specified|Kabuki_syndrome": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome|not_specified|not_provided": 1,
    "not_specified|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "Kabuki_syndrome|Kabuki_syndrome_1|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_1|not_provided|Lung_cancer": 1,
    "Inborn_genetic_diseases|not_provided|KMT2D-related_disorder|Kabuki_syndrome": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|Dystonia|_early-onset|_and/or_spastic_paraplegia|not_specified": 1,
    "Branchial_cleft_anomaly": 1,
    "Kabuki_syndrome|not_provided|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|Kabuki_syndrome_1|KMT2D-related_disorder": 1,
    "Kabuki_syndrome|Microcephaly": 1,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|not_specified|not_provided|Kabuki_syndrome": 1,
    "Kabuki_syndrome|not_specified|Kabuki_syndrome_1|KMT2D-related_disorder|not_provided": 1,
    "Kabuki_syndrome_1|KMT2D-related_disorder": 2,
    "Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome|KMT2D-related_disorder|Kabuki_syndrome|not_provided": 1,
    "Kabuki_syndrome|KMT2D-related_disorder|Kabuki_syndrome_1|Choanal_atresia-athelia-hypothyroidism-delayed_puberty-short_stature_syndrome": 1,
    "46|XY_sex_reversal_7": 53,
    "46|XY_sex_reversal_7|not_provided": 4,
    "DHH-related_disorder": 4,
    "not_provided|46|XY_sex_reversal_7": 3,
    "46|XY_sex_reversal_7|Inborn_genetic_diseases": 1,
    "46|XY_DSD/46|XY_CGD": 1,
    "46|XY_gonadal_dysgenesis-motor_and_sensory_neuropathy_syndrome": 5,
    "not_specified|46|XY_sex_reversal_7|not_provided": 2,
    "Inborn_genetic_diseases|46|XY_sex_reversal_7": 1,
    "DHH-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|46|XY_sex_reversal_7": 1,
    "not_provided|46|XY_sex_reversal_7|DHH-related_disorder": 1,
    "46|XY_sex_reversal_7|DHH-related_disorder": 1,
    "DSD_incomplete_virilization": 3,
    "TUBA1B-associated_neurodevelopmental_disorder": 1,
    "TUBA1A-associated_tubulinopathy|Tubulinopathy": 2,
    "not_provided|Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy": 2,
    "Lissencephaly|Polymicrogyria|Inborn_genetic_diseases|not_specified": 1,
    "Lissencephaly_due_to_TUBA1A_mutation": 63,
    "Tubulinopathy|Lissencephaly_due_to_TUBA1A_mutation": 12,
    "Tubulinopathy|Lissencephaly|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy": 1,
    "Tubulinopathy-associated_dysgyria": 1,
    "Tubulinopathy|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 4,
    "TUBA1A-related_disorder|not_specified|not_provided": 3,
    "TUBA1A-associated_tubulinopathy|Tubulinopathy|not_provided": 1,
    "TUBA1A-related_disorder|not_provided|not_specified": 2,
    "TUBA1A-related_disorder|not_provided": 3,
    "Cryptorchidism|Lissencephaly|Corpus_callosum|_agenesis_of|Tubulinopathy|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Lissencephaly_type_3": 3,
    "Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy|not_provided": 7,
    "Recurrent_hand_flapping": 1,
    "not_provided|Congenital_bilateral_perisylvian_syndrome|Congenital_fibrosis_of_extraocular_muscles": 1,
    "Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy": 8,
    "Tubulinopathy-associated_dysgyria|Tubulinopathy|not_provided|Lissencephaly|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided|Tubulinopathy|Lissencephaly|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "TUBA1A-related_disorder": 8,
    "not_specified|TUBA1A-related_disorder": 1,
    "not_specified|Congenital_bilateral_perisylvian_syndrome|Congenital_fibrosis_of_extraocular_muscles": 1,
    "Tubulinopathy|Lissencephaly_due_to_TUBA1A_mutation|not_provided": 1,
    "Rare_genetic_intellectual_disability|not_provided|Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy": 1,
    "Tubulinopathy|not_provided": 15,
    "Abnormal_cerebral_morphology|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Tubulinopathy|Abnormality_of_neuronal_migration|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Tubulinopathy|Inborn_genetic_diseases": 3,
    "Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy-associated_dysgyria": 1,
    "not_provided|TUBA1A-related_disorder": 4,
    "Tubulinopathy|Lissencephaly_due_to_TUBA1A_mutation|Lissencephaly": 1,
    "not_provided|Tubulinopathy-associated_dysgyria": 1,
    "Lissencephaly_due_to_TUBA1A_mutation|not_provided|Tubulinopathy|TUBA1A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Lissencephaly_due_to_TUBA1A_mutation": 6,
    "not_provided|Lissencephaly_due_to_TUBA1A_mutation|TUBA1A-related_disorder": 1,
    "not_provided|Abnormal_brainstem_morphology|Abnormal_cortical_gyration|Lissencephaly_type_3|TUBA1A-related_disorder": 1,
    "Lissencephaly_due_to_TUBA1A_mutation|not_provided": 4,
    "Tubulinopathy|Inborn_genetic_diseases|Lissencephaly|Lissencephaly_due_to_TUBA1A_mutation|not_provided": 1,
    "not_provided|Lissencephaly_type_3|Tubulinopathy": 1,
    "West_syndrome|Tubulinopathy-associated_dysgyria": 1,
    "Tubulinopathy-associated_dysgyria|not_provided|Corpus_callosum|_agenesis_of|Genetic_syndrome_with_a_Dandy-Walker_malformation_as_major_feature|Lissencephaly_due_to_TUBA1A_mutation|Dandy-Walker_syndrome|TUBA1A-related_disorder|Tubulinopathy|Inborn_genetic_diseases": 1,
    "Tubulinopathy|Inborn_genetic_diseases|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Early_myoclonic_encephalopathy|Tubulinopathy-associated_dysgyria|Continuous_spike_and_waves_during_slow_sleep|Tubulinopathy|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Tubulinopathy-associated_dysgyria|not_provided|Lissencephaly_due_to_TUBA1A_mutation|Tubulinopathy|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Tubulinopathy|not_provided|Movement_disorder": 1,
    "Lissencephaly_due_to_TUBA1A_mutation|not_specified|TUBA1A-related_disorder|not_provided": 1,
    "not_provided|Tubulinopathy|Inborn_genetic_diseases": 1,
    "not_provided|Lissencephaly_due_to_TUBA1A_mutation|Cerebral_palsy|Tubulinopathy|Inborn_genetic_diseases": 1,
    "Lissencephaly_due_to_LIS1_mutation|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "not_specified|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "TUBA1A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "not_specified|TUBA1A-related_disorder|not_provided": 1,
    "not_provided|Lissencephaly_type_3": 1,
    "not_provided|TUBA1A-associated_tubulinopathy": 1,
    "Congenital_cerebellar_hypoplasia|Cerebellar_vermis_hypoplasia|Lissencephaly_due_to_TUBA1A_mutation|Corpus_callosum|_agenesis_of": 1,
    "not_specified|not_provided|TUBA1A-related_disorder": 1,
    "Lissencephaly_due_to_TUBA1A_mutation|not_specified|not_provided|Tubulinopathy": 1,
    "Tubulinopathy-associated_dysgyria|Inborn_genetic_diseases|Global_developmental_delay|Decreased_head_circumference|Seizure|Neurodevelopmental_disorder|TUBA1A-related_disorder|Tubulinopathy|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Lissencephaly_due_to_TUBA1A_mutation|TUBA1A-related_disorder|not_provided": 1,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "not_provided|PRPH-related_disorder": 3,
    "not_provided|Amyotrophic_lateral_sclerosis|_susceptibility_to": 2,
    "PRPH-related_disorder|not_provided|not_specified|Amyotrophic_lateral_sclerosis|_susceptibility_to": 1,
    "PRPH-related_disorder|not_provided": 1,
    "not_provided|Oromandibular-limb_hypogenesis_spectrum": 1,
    "Diabetes_insipidus|_nephrogenic|_autosomal": 114,
    "Diabetes_insipidus|_nephrogenic|_autosomal|not_provided": 20,
    "not_provided|Diabetes_insipidus|_nephrogenic|_autosomal": 20,
    "Nephrogenic_diabetes_insipidus": 33,
    "Diabetes_insipidus|_nephrogenic|_autosomal|not_provided|Nephrogenic_diabetes_insipidus|not_specified": 1,
    "not_provided|Diabetes_insipidus|_nephrogenic|_autosomal|Nephrogenic_diabetes_insipidus": 3,
    "Nephrogenic_diabetes_insipidus|Diabetes_insipidus|_nephrogenic|_autosomal|not_provided": 4,
    "Diabetes_insipidus|_nephrogenic|_autosomal|Nephrogenic_diabetes_insipidus": 2,
    "Diabetes_insipidus|_nephrogenic|_autosomal|Nephrogenic_diabetes_insipidus|not_provided": 1,
    "not_provided|Nephrogenic_diabetes_insipidus": 10,
    "Nephrogenic_diabetes_insipidus|Diabetes_insipidus|_nephrogenic|_autosomal|not_specified|not_provided": 2,
    "Nephrogenic_diabetes_insipidus|not_provided|Diabetes_insipidus|_nephrogenic|_autosomal": 2,
    "AQP2-related_disorder": 1,
    "not_provided|not_specified|Nephrogenic_diabetes_insipidus|Diabetes_insipidus|_nephrogenic|_autosomal": 1,
    "Nephrogenic_diabetes_insipidus|not_specified|Diabetes_insipidus|_nephrogenic|_autosomal|not_provided": 1,
    "Diabetes_insipidus|not_provided|Diabetes_insipidus|_nephrogenic|_autosomal": 1,
    "Inborn_genetic_diseases|Diabetes_insipidus|_nephrogenic|_autosomal": 6,
    "not_provided|Diabetes_insipidus|_nephrogenic|_autosomal|not_specified": 1,
    "not_provided|Nephrogenic_diabetes_insipidus|Diabetes_insipidus|_nephrogenic|_autosomal": 3,
    "Nephrogenic_diabetes_insipidus|not_provided": 3,
    "not_specified|Diabetes_insipidus|_nephrogenic|_autosomal|not_provided|Nephrogenic_diabetes_insipidus": 1,
    "Diabetes_insipidus|_nephrogenic|_autosomal|not_specified": 1,
    "Nephrogenic_diabetes_insipidus|Diabetes_insipidus|_nephrogenic|_autosomal": 1,
    "Nephrogenic_diabetes_insipidus|AQP2-related_disorder|not_provided": 1,
    "Diabetes_insipidus|_nephrogenic|_autosomal|Hereditary_disease|not_provided": 1,
    "Diabetes_insipidus|_nephrogenic|_autosomal|not_provided|Nephrogenic_diabetes_insipidus": 1,
    "AQP5-related_disorder|Palmoplantar_keratoderma|_Bothnian_type|not_provided": 1,
    "not_provided|Palmoplantar_keratoderma|_Bothnian_type": 1,
    "Palmoplantar_keratoderma|_Bothnian_type": 4,
    "AQP5-related_disorder": 1,
    "Palmoplantar_keratoderma|_Bothnian_type|not_provided": 1,
    "Anemia|_congenital_dyserythropoietic|_type_IIIb|Anemia|_congenital_dyserythropoietic|_type_IIIb|_autosomal_recessive": 2,
    "Anemia|_congenital_dyserythropoietic|_type_IIIb": 1,
    "Coffin-Siris_syndrome_11|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Coffin-Siris_syndrome_11": 1,
    "Coffin-Siris_syndrome_11|not_provided": 2,
    "Coffin-Siris_syndrome_11": 16,
    "not_provided|Coffin-Siris_syndrome_11": 1,
    "Coffin-Siris_syndrome_11|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Transient_infantile_hypertriglyceridemia_and_hepatosteatosis": 3,
    "Transient_infantile_hypertriglyceridemia_and_hepatosteatosis": 17,
    "not_provided|GPD1-related_disorder": 6,
    "not_provided|GPD1-related_disorder|Transient_infantile_hypertriglyceridemia_and_hepatosteatosis": 1,
    "Transient_infantile_hypertriglyceridemia_and_hepatosteatosis|not_provided": 1,
    "GPD1-related_disorder": 1,
    "Transient_infantile_hypertriglyceridemia_and_hepatosteatosis|GPD1-related_disorder|not_provided": 1,
    "GPD1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Transient_infantile_hypertriglyceridemia_and_hepatosteatosis": 1,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_10": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_10": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_10": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_10|not_provided": 1,
    "LIMA1-related_disorder": 5,
    "LOW_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_8": 2,
    "Intellectual_disability|_FRA12A_type": 22,
    "DIP2B-related_disorder": 15,
    "DIP2B-related_disorder|not_provided": 3,
    "not_provided|DIP2B-related_disorder": 3,
    "not_specified|Intellectual_disability|_FRA12A_type": 1,
    "Intellectual_disability|_FRA12A_type|not_provided": 5,
    "Intellectual_disability|_FRA12A_type|DIP2B-related_disorder|not_provided": 1,
    "DIP2B-related_disorder|not_specified": 1,
    "Generalized_non-motor_(absence)_seizure": 1,
    "Microcytic_anemia_with_liver_iron_overload": 68,
    "Microcytic_anemia_with_liver_iron_overload|not_provided": 11,
    "SLC11A2-related_disorder|not_provided": 1,
    "Microcytic_anemia_with_liver_iron_overload|not_provided|not_specified": 1,
    "not_provided|Microcytic_anemia_with_liver_iron_overload": 8,
    "SLC11A2-related_disorder|not_provided|Microcytic_anemia_with_liver_iron_overload": 2,
    "Inborn_genetic_diseases|Microcytic_anemia_with_liver_iron_overload": 2,
    "Microcytic_anemia_with_liver_iron_overload|not_provided|SLC11A2-related_disorder": 2,
    "SLC11A2-related_disorder|Microcytic_anemia_with_liver_iron_overload": 1,
    "SLC11A2-related_disorder": 2,
    "Microcytic_anemia_with_liver_iron_overload|SLC11A2-related_disorder": 1,
    "not_provided|SLC11A2-related_disorder|Microcytic_anemia_with_liver_iron_overload": 1,
    "TFCP2-related_disorder": 2,
    "not_provided|TFCP2-related_disorder": 1,
    "SCN8A-related_disorder": 12,
    "SCN8A-related_disorder|not_specified|not_provided": 1,
    "Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy|Myoclonus|_familial|_2|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia": 37,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Myoclonus|_familial|_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_13": 87,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy": 5,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy": 8,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13": 16,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy": 10,
    "SCN8A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy": 3,
    "Seizures|_benign_familial_infantile|_5|not_provided|Developmental_and_epileptic_encephalopathy|_13|SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Intellectual_disability|Seizures|_benign_familial_infantile|_5": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "SCN8A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Seizures|_benign_familial_infantile|_5": 1,
    "SCN8A-related_disorder|not_provided": 4,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Inborn_genetic_diseases|Cognitive_impairment_with_or_without_cerebellar_ataxia|not_specified": 1,
    "Malaria|_susceptibility_to|Developmental_and_epileptic_encephalopathy|_13": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "Seizures|_benign_familial_infantile|_5": 5,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13": 2,
    "Focal_clonic_seizure|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|SCN8A-related_disorder": 5,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Myoclonus|_familial|_2|Seizures|_benign_familial_infantile|_5": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia": 4,
    "Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|Developmental_and_epileptic_encephalopathy|_13": 1,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "SCN8A-related_epileptic_disorder|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_regression|Global_developmental_delay|Epileptic_encephalopathy|Generalized_tonic_seizure|Intellectual_disability|_severe|Developmental_stagnation_at_onset_of_seizures": 1,
    "Autosomal_recessive_inheritance|Global_developmental_delay|Seizure|not_provided": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|SCN8A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|SCN8A-related_complex_neurodevelopmental_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Epileptic_encephalopathy": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13": 4,
    "Global_developmental_delay|Seizure|Developmental_and_epileptic_encephalopathy|_13|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "not_specified|Seizures|_benign_familial_infantile|_5|not_provided|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "not_provided|SCN8A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia": 6,
    "Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|Seizure|Intellectual_disability": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Seizures|_benign_familial_infantile|_5": 1,
    "Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|SCN8A-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|SCN8A-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|SCN8A-related_disorder|not_provided": 3,
    "not_provided|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13": 4,
    "SCN8A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 5,
    "Developmental_and_epileptic_encephalopathy|SCN8A-related_disorder|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Myoclonus|_familial|_2": 1,
    "Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|not_provided|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_5": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 3,
    "SCN8A-related_neurodevelopmental_delay": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Spastic_ataxia|Developmental_and_epileptic_encephalopathy": 1,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_13": 1,
    "not_specified|SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|SCN8A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|not_specified": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_13": 4,
    "SCN8A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "not_provided|Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5": 1,
    "Myoclonus|_familial|_2|not_specified|Seizures|_benign_familial_infantile|_5|not_provided|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|not_specified|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|West_syndrome|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Intellectual_disability|_moderate|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_13|not_provided": 4,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13": 1,
    "COGNITIVE_IMPAIRMENT_WITHOUT_CEREBELLAR_ATAXIA|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Seizure|Global_developmental_delay": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy|Myoclonus|_familial|_2|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|not_specified": 1,
    "SCN8A-related_disorder|Inborn_genetic_diseases|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13": 4,
    "Developmental_and_epileptic_encephalopathy|See_cases": 3,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|not_provided|not_specified": 1,
    "not_provided|SCN8A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5": 1,
    "See_cases|not_provided|Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Inborn_genetic_diseases": 3,
    "Developmental_and_epileptic_encephalopathy|_13|not_provided|not_specified": 1,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|SCN8A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Hereditary_ataxia": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|Developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy": 1,
    "COGNITIVE_IMPAIRMENT_WITHOUT_CEREBELLAR_ATAXIA|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|SCN8A-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Seizures|_benign_familial_infantile|_5|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13": 1,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Autosomal_recessive_inheritance|Global_developmental_delay|Seizure": 1,
    "Myoclonus|_familial|_2|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|not_specified": 1,
    "SCN8A-related_disorder|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Choreoathetosis|Global_developmental_delay|Leukoencephalopathy|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Myoclonus|_familial|_2|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Cognitive_impairment_with_or_without_cerebellar_ataxia": 2,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13": 1,
    "not_provided|SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13|Epilepsy|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_13|not_provided|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy": 1,
    "SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Undetermined_early-onset_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|not_provided|Epilepsy|Seizure": 1,
    "Seizures|_benign_familial_infantile|_5|not_provided": 1,
    "Seizure|Intellectual_disability": 3,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Autism|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "SCN8A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_13": 1,
    "not_provided|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13": 1,
    "not_provided|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia|not_specified": 1,
    "Inborn_genetic_diseases|developmental_delay_with_seizures|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|not_provided": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|not_provided|Abnormal_cerebral_morphology": 1,
    "Autism|Seizure|Intellectual_disability|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Autosomal_recessive_inheritance|Global_developmental_delay|Seizure": 1,
    "Seizure|Infantile_spasms|Epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|Neurodevelopmental_disorder": 2,
    "not_provided|Cognitive_impairment_with_or_without_cerebellar_ataxia": 2,
    "Myoclonus|_familial|_2": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_5|Myoclonus|_familial|_2|Cognitive_impairment_with_or_without_cerebellar_ataxia|Developmental_and_epileptic_encephalopathy|_13": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_infantile|_5": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2|Seizures|_benign_familial_infantile|_5|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|Seizures|_benign_familial_infantile|_5|Cognitive_impairment_with_or_without_cerebellar_ataxia|Myoclonus|_familial|_2|Inborn_genetic_diseases": 1,
    "Bilateral_tonic-clonic_seizure": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|SCN8A-related_disorder": 1,
    "not_provided|SCN8A-related_disorder|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_5": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_infantile|_5": 2,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_13|See_cases|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_13|Cognitive_impairment_with_or_without_cerebellar_ataxia|Myoclonus|_familial|_2|Seizures|_benign_familial_infantile|_5|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|Focal_epilepsy|not_provided|Developmental_and_epileptic_encephalopathy|_13|Seizure": 1,
    "Myoclonus|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Complex_neurodevelopmental_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Cognitive_impairment_with_or_without_cerebellar_ataxia|not_provided": 1,
    "Cognitive_impairment_with_or_without_cerebellar_ataxia|Seizures|_benign_familial_infantile|_5|Developmental_and_epileptic_encephalopathy|_13|Myoclonus|_familial|_2": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_13|not_provided": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|not_specified|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2": 516,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 35,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified": 4,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 29,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 11,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype": 77,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder": 4,
    "not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2": 72,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|not_provided": 6,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Haemorrhagic_telangiectasia_2|Cardiovascular_phenotype": 1,
    "ACVRL1-related_disorder": 4,
    "ACVRL1-related_disorder|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype": 5,
    "ACVRL1-related_disorder|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 3,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2": 6,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Hereditary_hemorrhagic_telangiectasia": 1,
    "Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 11,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|ACVRL1-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|not_provided|See_cases": 1,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Cardiovascular_phenotype": 9,
    "not_provided|Spontaneous|_recurrent_epistaxis|Lip_telangiectasia|Oral_cavity_telangiectasia|Telangiectasia_of_the_skin|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "not_specified|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_hypertension|_primary|_1": 1,
    "not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|not_specified": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|Pulmonary_arterial_hypertension": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|ACVRL1-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Pulmonary_hypertension|_primary|_1|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "not_provided|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype": 1,
    "Pulmonary_hypertension|_primary|_1|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified": 1,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2": 4,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Thrombocytopenia|Abnormal_bleeding": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified|not_provided": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Heritable_pulmonary_arterial_hypertension": 1,
    "Telangiectasia|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Cardiovascular_phenotype|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia": 2,
    "Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Cardiovascular_phenotype|ACVRL1-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 1,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|Hereditary_hemorrhagic_telangiectasia": 1,
    "not_provided|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder": 1,
    "Cardiovascular_phenotype|Pulmonary_hypertension|_primary|_1|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Cardiovascular_phenotype|Pulmonary_hypertension|_primary|_1": 1,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Haemorrhagic_telangiectasia_2|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|ACVRL1-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Pulmonary_hypertension|_primary|_1|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Pulmonary_hypertension|_primary|_1": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_arterial_hypertension|Cardiovascular_phenotype": 1,
    "See_cases|Cardiovascular_phenotype|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|ACVRL1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified": 1,
    "not_provided|ACVRL1-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "ACVRL1-related_disorder|not_provided|Cardiovascular_phenotype|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|not_provided": 1,
    "ACVRL1-related_disorder|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_factor_VIII_deficiency_disease|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_hypertension|_primary|_1": 2,
    "Haemorrhagic_telangiectasia_2|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Cardiovascular_phenotype|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "not_provided|Cardiovascular_phenotype|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_2": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Hereditary_factor_VIII_deficiency_disease": 1,
    "Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|ACVRL1-related_disorder": 1,
    "ACVRL1-related_disorder|not_specified|Telangiectasia|_hereditary_hemorrhagic|_type_2|Cardiovascular_phenotype|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_specified|not_provided": 1,
    "ACVRL1-related_disorder|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided": 1,
    "Hereditary_hemorrhagic_telangiectasia|Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Pulmonary_hypertension|_primary|_1": 1,
    "ACVRL1-related_disorder|Cardiovascular_phenotype|Haemorrhagic_telangiectasia_2|not_provided|not_specified|Pulmonary_arterial_hypertension|Telangiectasia|_hereditary_hemorrhagic|_type_2|Thrombocytopenia|Abnormal_bleeding": 1,
    "Pulmonary_arterial_hypertension|not_specified|Cardiovascular_phenotype|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Pulmonary_arterial_hypertension|Telangiectasia|_hereditary_hemorrhagic|_type_2|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Epistaxis": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|not_provided|Pulmonary_arterial_hypertension": 1,
    "Hereditary_factor_VIII_deficiency_disease|Pulmonary_arterial_hypertension_related_to_hereditary_hemorrhagic_telangiectasia|Cardiovascular_phenotype|Telangiectasia|_hereditary_hemorrhagic|_type_2|Hereditary_hemorrhagic_telangiectasia|not_provided": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_2|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "KRT80-related_disorder|not_specified": 1,
    "not_provided|KRT86-related_disorder": 1,
    "KRT81-related_disorder": 1,
    "not_specified|Monilethrix-1": 2,
    "KRT81-related_disorder|not_specified": 1,
    "Monilethrix-1": 4,
    "Monilethrix-2|not_provided": 2,
    "Monilethrix|Monilethrix-1|not_provided": 1,
    "Monilethrix|not_provided": 11,
    "not_provided|Monilethrix": 29,
    "KRT86-related_disorder": 2,
    "Monilethrix": 32,
    "KRT83-related_disorder|not_provided|Monilethrix": 1,
    "KRT83-related_disorder": 5,
    "not_specified|Monilethrix-1|Erythrokeratodermia_variabilis_et_progressiva_5": 1,
    "not_specified|Monilethrix": 7,
    "not_provided|KRT83-related_disorder|Monilethrix": 4,
    "Monilethrix-3": 1,
    "Monilethrix-3|not_provided|Monilethrix": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_5|Monilethrix-1": 2,
    "Monilethrix|KRT83-related_disorder|not_provided": 1,
    "not_provided|KRT83-related_disorder": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_5|not_provided": 1,
    "not_provided|Monilethrix|not_specified": 1,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_5|Monilethrix": 1,
    "Monilethrix|not_specified": 2,
    "not_specified|not_provided|Monilethrix": 1,
    "Ectodermal_dysplasia_4|_hair/nail_type": 3,
    "KRT85-related_disorder": 6,
    "KRT85-related_disorder|not_provided": 4,
    "KRT85-related_disorder|not_specified": 1,
    "not_provided|Ectodermal_dysplasia_4|_hair/nail_type": 1,
    "not_provided|KRT85-related_disorder": 1,
    "not_specified|Ectodermal_dysplasia_4|_hair/nail_type|not_provided": 1,
    "KRT85-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|KRT85-related_disorder": 1,
    "KRT75-related_disorder": 12,
    "KRT75-related_disorder|not_provided": 1,
    "Pseudofolliculitis_barbae|KRT75-related_disorder|not_provided": 1,
    "not_provided|Pachyonychia_congenita_4": 2,
    "not_provided|KRT6B-related_disorder": 6,
    "Pachyonychia_congenita_4|not_provided": 5,
    "Pachyonychia_congenita_4": 2,
    "KRT6B-related_disorder|not_provided": 5,
    "KRT6B-related_disorder|not_provided|Pachyonychia_congenita_4": 3,
    "KRT6B-related_disorder": 10,
    "KRT6B-related_disorder|Pachyonychia_congenita_2|not_provided": 1,
    "KRT6C-related_disorder": 9,
    "not_provided|KRT6C-related_disorder": 2,
    "Palmoplantar_keratoderma|_nonepidermolytic|_focal_or_diffuse|KRT6C-related_disorder|not_provided": 2,
    "KRT6C-related_disorder|not_provided|Palmoplantar_keratoderma|_nonepidermolytic|_focal_or_diffuse": 3,
    "KRT6C-related_disorder|not_provided": 2,
    "not_provided|Palmoplantar_keratoderma|_nonepidermolytic|_focal_or_diffuse": 5,
    "not_provided|Focal_palmoplantar_keratoderma": 2,
    "KRT6C-related_disorder|Palmoplantar_keratoderma|_nonepidermolytic|_focal_or_diffuse|not_provided": 5,
    "Palmoplantar_keratoderma|_nonepidermolytic|_focal_or_diffuse|not_provided": 1,
    "Palmoplantar_keratoderma|_nonepidermolytic|_focal_or_diffuse": 1,
    "Pachyonychia_congenita_3|not_provided": 12,
    "KRT6A-related_disorder|not_provided": 5,
    "Pachyonychia_congenita_3": 11,
    "not_provided|Pachyonychia_congenita_3": 6,
    "KRT6A-related_disorder": 12,
    "not_specified|KRT6A-related_disorder|not_provided": 1,
    "not_provided|KRT6A-related_disorder": 1,
    "KRT6A-related_disorder|not_provided|Pachyonychia_congenita_3": 2,
    "Pachyonychia_congenita_3|not_provided|KRT6A-related_disorder": 1,
    "not_provided|KRT6A-related_disorder|Pachyonychia_congenita_3": 1,
    "Epidermolysis_bullosa_simplex|not_provided": 14,
    "KRT5-related_disorder": 6,
    "Epidermolysis_bullosa_simplex|not_provided|KRT5-related_disorder": 1,
    "Inborn_genetic_diseases|Epidermolysis_bullosa_simplex": 4,
    "not_provided|KRT5-related_disorder": 4,
    "Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema": 3,
    "Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|not_provided|KRT5-related_disorder": 1,
    "not_provided|KRT5-related_disorder|Epidermolysis_bullosa_simplex_1C|_localized": 1,
    "Epidermolysis_bullosa_simplex_2C|_localized|not_provided": 1,
    "not_specified|not_provided|Epidermolysis_bullosa_simplex": 3,
    "not_specified|Epidermolysis_bullosa_simplex|not_provided": 2,
    "Epidermolysis_bullosa_simplex|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa_simplex|not_provided|not_specified": 3,
    "EPIDERMOLYSIS_BULLOSA_SIMPLEX_2D|_GENERALIZED_SEVERE|_AUTOSOMAL_RECESSIVE|not_provided": 1,
    "KRT5-related_disorder|not_provided": 2,
    "Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Dowling-Degos_disease_1|Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|Epidermolysis_bullosa_simplex_2C|_localized|Epidermolysis_bullosa_simplex_2d|_generalized|_intermediate_or_severe|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_simplex_2A|_generalized_severe|not_provided": 2,
    "Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Epidermolysis_bullosa_simplex_1C|_localized|KRT5-related_disorder|Epidermolysis_bullosa_simplex|not_provided": 1,
    "Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|Epidermolysis_bullosa_simplex_1A|_generalized_severe|not_provided": 1,
    "Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|not_provided": 1,
    "Epidermolysis_bullosa_simplex_2A|_generalized_severe|not_provided|Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_1C|_localized|Epidermolysis_bullosa_simplex|_Koebner_type": 1,
    "Epidermolysis_bullosa_simplex_2B|_generalized_intermediate": 4,
    "not_provided|Epidermolysis_bullosa_simplex": 11,
    "Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|Epidermolysis_bullosa_simplex_2C|_localized|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Koebner_type": 2,
    "not_provided|Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate": 2,
    "not_provided|Epidermolysis_bullosa_simplex_2C|_localized|_modifier_of": 1,
    "Epidermolysis_bullosa_simplex|KRT5-related_disorder|not_provided": 2,
    "Epidermolysis_bullosa_simplex_2C|_localized|Dowling-Degos_disease_1|Epidermolysis_bullosa_simplex_2d|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|Epidermolysis_bullosa_simplex_with_mottled_pigmentation": 4,
    "not_provided|Epidermolysis_bullosa_simplex|KRT5-related_disorder": 1,
    "Epidermolysis_bullosa|not_provided|KRT5-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_1C|_localized|Dowling-Degos_disease_1": 1,
    "not_provided|Epidermolysis_bullosa_simplex_2C|_localized": 1,
    "Epidermolysis_bullosa_simplex_2C|_localized|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1C|_localized|Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Dowling-Degos_disease_1|not_provided|KRT5-related_disorder": 1,
    "Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|not_provided": 1,
    "EPIDERMOLYSIS_BULLOSA_SIMPLEX_2D|_GENERALIZED_SEVERE|_AUTOSOMAL_RECESSIVE|Epidermolysis_bullosa_simplex": 1,
    "Epidermolysis_bullosa_simplex_2C|_localized|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Dowling-Degos_disease_1|Epidermolysis_bullosa_simplex_2d|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|Inborn_genetic_diseases": 1,
    "not_provided|KRT5-related_disorder|Epidermolysis_bullosa_simplex": 2,
    "Epidermolysis_bullosa_simplex|not_specified|not_provided": 2,
    "Dowling-Degos_disease_1|not_provided": 3,
    "Dowling-Degos_disease_1|Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|Epidermolysis_bullosa_simplex_2C|_localized|Epidermolysis_bullosa_simplex_2d|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Epidermolysis_bullosa_simplex_1A|_generalized_severe|not_specified|Epidermolysis_bullosa_simplex|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_2C|_localized": 1,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|not_provided": 3,
    "not_provided|not_specified|Epidermolysis_bullosa_simplex": 1,
    "not_provided|Epidermolysis_bullosa_simplex|not_specified": 2,
    "not_provided|Epidermolysis_bullosa_simplex_2A|_generalized_severe": 2,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe": 5,
    "not_provided|Epidermolysis_bullosa_simplex_with_mottled_pigmentation": 1,
    "not_provided|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate": 1,
    "Epidermolysis_bullosa_simplex_2d|_generalized|_intermediate_or_severe|_autosomal_recessive": 1,
    "not_provided|KRT5-related_disorder|Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_2C|_localized": 1,
    "Epidermolysis_bullosa_simplex_2C|_localized|Epidermolysis_bullosa_simplex_1C|_localized|KRT5-related_disorder|not_provided": 1,
    "EPIDERMOLYSIS_BULLOSA_SIMPLEX_2D|_GENERALIZED_INTERMEDIATE|_AUTOSOMAL_RECESSIVE": 1,
    "Inborn_genetic_diseases|Dowling-Degos_disease_1": 1,
    "KRT5-related_disorder|not_provided|Epidermolysis_bullosa_simplex": 2,
    "Epidermolysis_bullosa_simplex_2C|_localized|Dowling-Degos_disease_1|Epidermolysis_bullosa_simplex_2d|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|Epidermolysis_bullosa_simplex_2A|_generalized_severe|Epidermolysis_bullosa_simplex_with_migratory_circinate_erythema|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Epidermolysis_bullosa_simplex_2B|_generalized_intermediate|not_provided|Epidermolysis_bullosa_simplex": 1,
    "KRT5-related_disorder|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex_with_mottled_pigmentation|not_provided|Epidermolysis_bullosa_simplex": 1,
    "KRT5-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|KRT71-related_disorder|not_provided": 2,
    "KRT71-related_disorder|not_provided": 4,
    "not_provided|KRT71-related_disorder": 5,
    "Hypotrichosis_13|not_specified": 1,
    "not_specified|Hypotrichosis_13": 2,
    "KRT71-related_disorder": 2,
    "Hypotrichosis_13|not_specified|not_provided": 1,
    "Hypotrichosis_13": 1,
    "KRT74-related_disorder|not_specified": 1,
    "not_provided|KRT74-related_disorder": 6,
    "KRT74-related_disorder|not_provided": 2,
    "KRT74-related_disorder": 3,
    "not_provided|Hypotrichosis_3": 1,
    "not_provided|Autosomal_dominant_wooly_hair": 1,
    "Autosomal_dominant_wooly_hair|not_provided": 2,
    "Ectodermal_dysplasia_4|_hair/nail_type|Ectodermal_dysplasia_7|_hair/nail_type|Autosomal_dominant_wooly_hair|Hypotrichosis_3|not_provided|KRT74-related_disorder": 1,
    "not_specified|not_provided|Autosomal_dominant_wooly_hair|Hypotrichosis_3|Ectodermal_dysplasia_7|_hair/nail_type": 1,
    "Ichthyosis_bullosa_of_Siemens": 46,
    "Ichthyosis_bullosa_of_Siemens|not_provided": 23,
    "Inborn_genetic_diseases|Ichthyosis_bullosa_of_Siemens": 3,
    "Ichthyosis_bullosa_of_Siemens|KRT2-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|KRT2-related_disorder": 1,
    "not_provided|Ichthyosis_bullosa_of_Siemens|Exfoliative_ichthyosis": 1,
    "not_provided|Ichthyosis_bullosa_of_Siemens": 4,
    "KRT2-related_disorder": 2,
    "not_provided|KRT2-related_disorder": 1,
    "Ichthyosis_bullosa_of_Siemens|KRT2-related_disorder": 1,
    "KRT2-related_disorder|not_provided": 3,
    "Diffuse_nonepidermolytic_palmoplantar_keratoderma|Epidermolytic_ichthyosis": 13,
    "not_provided|Epidermolytic_ichthyosis|Diffuse_nonepidermolytic_palmoplantar_keratoderma": 1,
    "Epidermolytic_ichthyosis|Diffuse_nonepidermolytic_palmoplantar_keratoderma": 4,
    "Epidermolytic_hyperkeratosis_1": 4,
    "Epidermolytic_ichthyosis|Inborn_genetic_diseases|Diffuse_nonepidermolytic_palmoplantar_keratoderma": 1,
    "not_provided|Diffuse_nonepidermolytic_palmoplantar_keratoderma|Epidermolytic_ichthyosis": 10,
    "Congenital_reticular_ichthyosiform_erythroderma": 8,
    "Ichthyosis_hystrix_of_Curth-Macklin": 2,
    "Ichthyosis|_annular_epidermolytic_1|not_provided": 1,
    "KRT1-related_disorder": 7,
    "not_provided|Epidermolytic_ichthyosis": 6,
    "KRT1-related_disorder|not_provided": 5,
    "Diffuse_nonepidermolytic_palmoplantar_keratoderma|KRT1-related_disorder|Epidermolytic_ichthyosis": 1,
    "not_provided|Diffuse_nonepidermolytic_palmoplantar_keratoderma|KRT1-related_disorder|Epidermolytic_ichthyosis": 3,
    "Diffuse_nonepidermolytic_palmoplantar_keratoderma|Epidermolytic_ichthyosis|not_provided": 2,
    "not_provided|Keratosis_palmoplantaris_striata_3": 1,
    "not_provided|Ichthyosis_hystrix_of_Curth-Macklin": 2,
    "Diffuse_nonepidermolytic_palmoplantar_keratoderma|Annular_epidermolytic_ichthyosis|Epidermolytic_ichthyosis|Keratosis_palmoplantaris_striata_3|Ichthyosis_hystrix_of_Curth-Macklin|Palmoplantar_keratoderma|_epidermolytic|not_provided": 1,
    "Annular_epidermolytic_ichthyosis|Ichthyosis|_annular_epidermolytic|_2|not_provided|KRT1-related_disorder": 1,
    "Ichthyosis|_annular_epidermolytic|_2|not_provided": 1,
    "not_provided|Epidermolytic_hyperkeratosis_1": 2,
    "KRT1-related_disorder|Epidermolytic_ichthyosis": 1,
    "not_provided|Diffuse_nonepidermolytic_palmoplantar_keratoderma": 3,
    "Diffuse_nonepidermolytic_palmoplantar_keratoderma": 2,
    "Palmoplantar_keratoderma|_epidermolytic|_2|not_provided": 2,
    "KRT1-related_disorder|Diffuse_nonepidermolytic_palmoplantar_keratoderma|Epidermolytic_ichthyosis|not_provided": 1,
    "not_provided|Diffuse_nonepidermolytic_palmoplantar_keratoderma|not_specified|Epidermolytic_ichthyosis": 1,
    "Epidermolytic_ichthyosis": 4,
    "Ichthyosis|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|KRT1-related_disorder": 1,
    "Epidermolytic_hyperkeratosis_1|not_provided": 2,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma|_epidermolytic|_2": 1,
    "Annular_epidermolytic_ichthyosis": 2,
    "KRT1-related_disorder|not_provided|Epidermolytic_ichthyosis": 1,
    "not_provided|Palmoplantar_keratoderma|_epidermolytic|_2|Ichthyosis|_annular_epidermolytic|_2": 1,
    "Annular_epidermolytic_ichthyosis|not_provided": 2,
    "not_provided|KRT1-related_disorder": 1,
    "Diffuse_nonepidermolytic_palmoplantar_keratoderma|not_provided|Epidermolytic_ichthyosis": 1,
    "not_provided|Diffuse_nonepidermolytic_palmoplantar_keratoderma|KRT1-related_disorder|Epidermolytic_ichthyosis|not_specified": 1,
    "KRT3-related_disorder|not_provided": 2,
    "KRT3-related_disorder": 8,
    "Corneal_dystrophy|_Meesmann|_2": 3,
    "Corneal_dystrophy|_Meesmann|_2|not_provided": 4,
    "not_provided|KRT3-related_disorder": 2,
    "Corneal_dystrophy|_Meesmann|_2|not_specified": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea": 10,
    "White_sponge_nevus_1": 47,
    "not_provided|White_sponge_nevus_1": 14,
    "Inborn_genetic_diseases|White_sponge_nevus_1": 13,
    "Inborn_genetic_diseases|not_provided|White_sponge_nevus_1": 1,
    "KRT4-related_disorder": 2,
    "White_sponge_nevus_1|not_provided|KRT4-related_disorder": 1,
    "White_sponge_nevus_1|Inborn_genetic_diseases": 2,
    "not_provided|White_sponge_nevus_1|KRT4-related_disorder": 5,
    "not_provided|Inborn_genetic_diseases|White_sponge_nevus_1": 1,
    "White_sponge_nevus_1|KRT4-related_disorder": 1,
    "not_provided|KRT8-related_disorder": 3,
    "not_specified|Hepatitis_C_virus|_susceptibility_to": 1,
    "not_provided|Hepatitis_C_virus|_susceptibility_to": 1,
    "KRT8-related_disorder": 4,
    "KRT8-related_disorder|not_provided": 2,
    "Inflammatory_bowel_disease|not_specified|not_provided|Hepatitis_C_virus|_susceptibility_to": 1,
    "not_specified|Cirrhosis|_cryptogenic|not_provided": 1,
    "Cirrhosis|_cryptogenic|Hepatitis_C_virus|_susceptibility_to|not_provided|not_specified": 1,
    "not_provided|Cirrhosis|_familial": 1,
    "not_provided|Cirrhosis|_cryptogenic|Cirrhosis|_noncryptogenic|_susceptibility_to": 1,
    "Cirrhosis|_familial": 2,
    "TNS2-related_disorder": 17,
    "TNS2-related_disorder|not_provided": 21,
    "not_provided|TNS2-related_disorder": 14,
    "not_specified|TNS2-related_disorder|not_provided": 2,
    "not_provided|TNS2-related_disorder|not_specified": 2,
    "TNS2-related_disorder|not_specified": 2,
    "not_provided|not_specified|TNS2-related_disorder": 1,
    "ESPL1-related_disorder": 16,
    "not_provided|ESPL1-related_disorder": 1,
    "ESPL1-related_disorder|not_provided": 3,
    "Glucocorticoid_deficiency_with_achalasia": 48,
    "not_provided|Glucocorticoid_deficiency_with_achalasia": 41,
    "not_provided|AAAS-related_disorder|Glucocorticoid_deficiency_with_achalasia": 2,
    "Inborn_genetic_diseases|not_provided|Glucocorticoid_deficiency_with_achalasia": 2,
    "Glucocorticoid_deficiency_with_achalasia|not_provided": 14,
    "Neurodevelopmental_disorder|not_provided|Glucocorticoid_deficiency_with_achalasia": 1,
    "Achalasia-alacrima_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Glucocorticoid_deficiency_with_achalasia": 1,
    "not_provided|AAAS-related_disorder": 1,
    "Glucocorticoid_deficiency_with_achalasia|not_provided|Inborn_genetic_diseases": 1,
    "Glucocorticoid_deficiency_with_achalasia|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|Glucocorticoid_deficiency_with_achalasia": 2,
    "Inborn_genetic_diseases|Glucocorticoid_deficiency_with_achalasia": 2,
    "Inborn_genetic_diseases|Hyperreflexia|Babinski_sign|Spastic_paraparesis|not_provided|Glucocorticoid_deficiency_with_achalasia": 1,
    "Glucocorticoid_deficiency_with_achalasia|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Microcephaly|Abnormality_of_the_nervous_system": 1,
    "AAAS-related_disorder": 1,
    "not_provided|Glucocorticoid_deficiency_with_achalasia|AAAS-related_disorder": 2,
    "not_specified|not_provided|AAAS-related_disorder|Inborn_genetic_diseases": 1,
    "Achalasia-alacrima_syndrome|not_provided|Glucocorticoid_deficiency_with_achalasia": 1,
    "Glucocorticoid_deficiency_with_achalasia|not_specified": 1,
    "AAAS-related_disorder|Inborn_genetic_diseases|not_provided|Glucocorticoid_deficiency_with_achalasia": 1,
    "Osteogenesis_imperfecta_type_12|not_provided": 5,
    "not_provided|Osteogenesis_imperfecta_type_12": 4,
    "not_provided|Osteogenesis_imperfecta_type_12|not_specified": 1,
    "Osteogenesis_imperfecta_type_12|not_provided|not_specified": 1,
    "SP7-related_disorder|not_provided": 2,
    "Osteogenesis_imperfecta_type_12|Osteogenesis_imperfecta|not_provided": 1,
    "Osteogenesis_imperfecta_type_12": 6,
    "Osteogenesis_imperfecta|not_specified|not_provided|Osteogenesis_imperfecta_type_12": 1,
    "SP7-related_disorder": 3,
    "Osteogenesis_imperfecta_type_12|not_specified": 1,
    "not_provided|SP7-related_disorder": 1,
    "Osteogenesis_Imperfecta|_Recessive|not_specified": 1,
    "Persistent_Mullerian_duct_syndrome": 28,
    "not_provided|Persistent_Mullerian_duct_syndrome": 5,
    "Persistent_mullerian_duct_syndrome|_type_II": 2,
    "AMHR2-related_disorder|not_provided": 3,
    "Persistent_Mullerian_duct_syndrome|Genetic_non-acquired_premature_ovarian_failure": 1,
    "Persistent_Mullerian_duct_syndrome|Male_pseudohermaphroditism": 1,
    "not_provided|Persistent_mullerian_duct_syndrome|_type_II": 1,
    "Persistent_mullerian_duct_syndrome|_type_II|Persistent_Mullerian_duct_syndrome|not_provided": 1,
    "Persistent_Mullerian_duct_syndrome|not_provided": 5,
    "Inborn_genetic_diseases|Persistent_Mullerian_duct_syndrome": 1,
    "Falls|Delayed_speech_and_language_development": 1,
    "HOXC13-related_disorder|not_provided": 1,
    "HOXC13-related_disorder|not_specified": 1,
    "Ectodermal_dysplasia_9|_hair/nail_type": 6,
    "HOXC13-related_disorder": 1,
    "Ectodermal_dysplasia_9|_hair/nail_type|not_provided": 1,
    "HNRNPA1-related_disorder": 15,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_3": 3,
    "HNRNPA1-related_disorder|not_provided": 4,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_3|Amyotrophic_lateral_sclerosis_type_20|not_provided": 1,
    "not_provided|HNRNPA1-related_disorder": 2,
    "Inclusion_body_myopathy_with_Paget_disease_of_bone_and_frontotemporal_dementia": 1,
    "Relapsing_remitting_multiple_sclerosis": 7,
    "Amyotrophic_lateral_sclerosis_type_20|not_provided": 2,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_3|not_provided": 1,
    "Chronic_progressive_multiple_sclerosis": 18,
    "Inclusion_body_myopathy_with_early-onset_Paget_disease_with_or_without_frontotemporal_dementia_3|Amyotrophic_lateral_sclerosis_type_20|Finnish_upper_limb-onset_distal_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|HNRNPA1-related_disorder": 1,
    "Chronic_progressive_multiple_sclerosis|not_provided": 1,
    "HNRNPA1-related_multisystem_proteinopathy": 1,
    "Finnish_upper_limb-onset_distal_myopathy": 1,
    "NCKAP1L-related_disorder|not_provided": 4,
    "not_specified|NCKAP1L-related_disorder|not_provided": 1,
    "NCKAP1L-related_disorder": 1,
    "Immunodeficiency_72_with_autoinflammation|not_provided": 2,
    "not_provided|Immunodeficiency_72_with_autoinflammation": 1,
    "not_specified|Immunodeficiency_72_with_autoinflammation": 1,
    "not_provided|NCKAP1L-related_disorder": 1,
    "Cerebellar_ataxia|Intellectual_disability|_moderate|Hypotonia|Delayed_speech_and_language_development": 2,
    "not_specified|Low-frequency_hearing_loss|Low-frequency_sensorineural_hearing_impairment": 1,
    "Congenital_Muscular_Dystrophy|_ITGA7-related": 1,
    "not_specified|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 48,
    "not_specified|not_provided|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 16,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_specified": 49,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_provided": 26,
    "not_provided|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 34,
    "not_provided|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|ITGA7-related_disorder": 1,
    "not_provided|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_specified": 6,
    "not_provided|not_specified|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 8,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_specified|not_provided": 15,
    "not_specified|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_provided": 6,
    "ITGA7-related_disorder|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_specified|not_provided": 1,
    "ITGA7-related_disorder|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 1,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|ITGA7-related_disorder": 5,
    "ITGA7-related_disorder|not_specified|not_provided|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 7,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_provided|not_specified": 5,
    "ITGA7-related_disorder|not_provided|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 3,
    "not_specified|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|ITGA7-related_disorder": 1,
    "ITGA7-related_disorder": 4,
    "ITGA7-related_disorder|not_specified|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 1,
    "not_provided|ITGA7-related_disorder|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_specified": 1,
    "not_specified|not_provided|ITGA7-related_disorder|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 1,
    "not_provided|ITGA7-related_disorder|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency": 2,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_provided|ITGA7-related_disorder": 1,
    "Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|Congenital_Muscular_Dystrophy|_ITGA7-related": 1,
    "ITGA7-related_disorder|Congenital_muscular_dystrophy_due_to_integrin_alpha-7_deficiency|not_provided": 1,
    "Pigmentary_retinal_dystrophy|not_specified": 2,
    "Pigmentary_retinal_dystrophy|not_provided": 8,
    "not_provided|Pigmentary_retinal_dystrophy|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Pigmentary_retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Pigmentary_retinal_dystrophy": 1,
    "Pigmentary_retinal_dystrophy|Optic_atrophy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Fundus_albipunctatus|_autosomal_recessive": 1,
    "not_provided|Pigmentary_retinal_dystrophy|Fundus_albipunctatus|_autosomal_recessive": 2,
    "not_provided|not_specified|Pigmentary_retinal_dystrophy": 1,
    "not_provided|Fundus_albipunctatus|_autosomal_recessive|Pigmentary_retinal_dystrophy": 1,
    "not_specified|not_provided|Pigmentary_retinal_dystrophy": 1,
    "Fundus_albipunctatus|_autosomal_recessive": 2,
    "Retinal_dystrophy|Pigmentary_retinal_dystrophy|not_provided": 1,
    "not_specified|Pigmentary_retinal_dystrophy|not_provided": 1,
    "Pigmentary_retinal_dystrophy|not_provided|not_specified": 1,
    "not_provided|Retinal_dystrophy|Pigmentary_retinal_dystrophy": 1,
    "Retinitis_punctata_albescens|not_provided": 1,
    "RDH5-related_disorder|Congenital_stationary_night_blindness|Retinal_dystrophy|not_provided|Pigmentary_retinal_dystrophy|Retinitis_punctata_albescens|Fundus_albipunctatus|_autosomal_recessive|See_cases": 1,
    "not_provided|Fundus_albipunctatus|_autosomal_recessive|Congenital_stationary_night_blindness|Pigmentary_retinal_dystrophy": 1,
    "Fundus_albipunctatus|_autosomal_recessive|not_provided|Pigmentary_retinal_dystrophy": 1,
    "GDF11-related_disorder": 2,
    "Vertebral_hypersegmentation_and_orofacial_anomalies": 4,
    "GDF11-related_disorder|not_provided": 1,
    "Vertebral_hypersegmentation_and_orofacial_anomalies|Orofacial_cleft": 1,
    "Vertebral_hypersegmentation_and_orofacial_anomalies|not_specified": 1,
    "GDF11-associated_multiple_congenital_anomalies_and_ID": 1,
    "Familial_cavitary_optic_disk_anomaly": 4,
    "not_specified|Familial_cavitary_optic_disk_anomaly": 2,
    "MMP19-related_disorder|not_provided": 1,
    "not_provided|Familial_cavitary_optic_disk_anomaly": 1,
    "MMP19-related_disorder": 1,
    "Familial_cavitary_optic_disk_anomaly|not_provided": 1,
    "DGKA-related_disorder": 10,
    "DGKA-related_disorder|not_provided": 1,
    "PMEL-related_disorder": 2,
    "PMEL-related_disorder|not_provided": 1,
    "not_specified|PMEL-related_disorder": 1,
    "not_provided|RAB5B-associated_surfactant_dysfunction_disorder": 1,
    "not_provided|Sulfite_oxidase_deficiency": 11,
    "Sulfite_oxidase_deficiency": 405,
    "Inborn_genetic_diseases|Sulfite_oxidase_deficiency": 12,
    "Sulfite_oxidase_deficiency|Sulfocysteinuria": 4,
    "SUOX-related_disorder|Sulfite_oxidase_deficiency": 5,
    "SUOX-related_disorder|Sulfocysteinuria|Sulfite_oxidase_deficiency": 1,
    "Sulfite_oxidase_deficiency|Inborn_genetic_diseases": 14,
    "Inborn_genetic_diseases|SUOX-related_disorder|not_specified|Sulfite_oxidase_deficiency": 1,
    "Sulfocysteinuria|SUOX-related_disorder|Inborn_genetic_diseases|Sulfite_oxidase_deficiency": 1,
    "Sulfite_oxidase_deficiency|not_provided": 2,
    "not_provided|Sulfite_oxidase_deficiency|SUOX-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Sulfite_oxidase_deficiency": 1,
    "Sulfite_oxidase_deficiency|Inborn_genetic_diseases|SUOX-related_disorder": 1,
    "Sulfocysteinuria": 1,
    "not_specified|Sulfite_oxidase_deficiency": 2,
    "Inborn_genetic_diseases|not_provided|Sulfocysteinuria|SUOX-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Sulfite_oxidase_deficiency": 1,
    "not_provided|Sulfocysteinuria|Inborn_genetic_diseases|Sulfite_oxidase_deficiency": 1,
    "not_provided|Sulfite_oxidase_deficiency|Sulfocysteinuria": 1,
    "Sulfite_oxidase_deficiency|SUOX-related_disorder": 1,
    "not_specified|not_provided|Sulfite_oxidase_deficiency": 1,
    "not_provided|Sulfite_oxidase_deficiency|SUOX-related_disorder|not_specified": 1,
    "SUOX-related_disorder|not_specified|not_provided|Sulfite_oxidase_deficiency": 1,
    "Sulfocysteinuria|Sulfite_oxidase_deficiency": 1,
    "Sulfite_oxidase_deficiency|not_specified|not_provided": 1,
    "Diamond-Blackfan_anemia_10": 109,
    "not_specified|Diamond-Blackfan_anemia_10": 3,
    "not_specified|Diamond-Blackfan_anemia_10|not_provided": 1,
    "not_specified|not_provided|Diamond-Blackfan_anemia_10": 1,
    "RPS26-related_disorder": 5,
    "RPS26-related_disorder|not_specified|not_provided|Diamond-Blackfan_anemia_10": 1,
    "not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_10": 1,
    "not_provided|Diamond-Blackfan_anemia_10": 3,
    "Diamond-Blackfan_anemia_10|Diamond-Blackfan_anemia": 7,
    "Diamond-Blackfan_anemia_10|not_specified": 2,
    "Diamond-Blackfan_anemia_15_with_mandibulofacial_dysostosis|Diamond-Blackfan_anemia_10": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_10": 2,
    "RPS26-related_disorder|Diamond-Blackfan_anemia_10": 1,
    "not_specified|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_10": 1,
    "Diamond-Blackfan_anemia_10|RPS26-related_disorder": 2,
    "Diamond-Blackfan_anemia_15_with_mandibulofacial_dysostosis|Diamond-Blackfan_anemia_10|Diamond-Blackfan_anemia": 1,
    "Pure_red-cell_aplasia|Anemia": 1,
    "not_specified|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_10|not_provided": 1,
    "Diamond-Blackfan_anemia_10|not_provided": 2,
    "Erythroleukemia|_familial|_susceptibility_to|Lethal_congenital_contracture_syndrome_2|Visceral_neuropathy|_familial|_1|_autosomal_recessive": 3,
    "ERBB3-related_disorder|Erythroleukemia|_familial|_susceptibility_to|Lethal_congenital_contracture_syndrome_2|Visceral_neuropathy|_familial|_1|_autosomal_recessive|not_provided": 1,
    "ERBB3-related_disorder|not_provided": 4,
    "ERBB3-related_disorder": 16,
    "not_provided|Lethal_congenital_contracture_syndrome_2|Visceral_neuropathy|_familial": 2,
    "Lethal_congenital_contracture_syndrome_2": 4,
    "not_provided|ERBB3-related_disorder": 2,
    "not_provided|Lethal_congenital_contracture_syndrome_2": 1,
    "Visceral_neuropathy|_familial|_1|_autosomal_recessive": 7,
    "not_specified|Lethal_congenital_contracture_syndrome_2": 1,
    "Erythroleukemia|_familial|_susceptibility_to|Lethal_congenital_contracture_syndrome_2|Visceral_neuropathy|_familial|_1|_autosomal_recessive|not_provided": 1,
    "not_provided|Visceral_neuropathy|_familial|Lethal_congenital_contracture_syndrome_2": 1,
    "Visceral_neuropathy|_familial|not_provided|Lethal_congenital_contracture_syndrome_2": 1,
    "Visceral_neuropathy|_familial|_1|_autosomal_recessive|Lethal_congenital_contracture_syndrome_2|not_provided": 1,
    "not_provided|Lethal_congenital_contracture_syndrome_1": 1,
    "not_specified|Erythroleukemia|_familial|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Coffin-Siris_syndrome_8": 1,
    "SMARCC2-related_disorder|not_provided|not_specified": 1,
    "SMARCC2-related_disorder|not_provided|Coffin-Siris_syndrome_8": 2,
    "Coffin-Siris_syndrome_8": 50,
    "SMARCC2-related_disorder": 19,
    "Coffin-Siris_syndrome_8|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|SMARCC2-related_disorder": 1,
    "not_provided|SMARCC2-related_disorder|Coffin-Siris_syndrome_8": 1,
    "not_provided|Coffin-Siris_syndrome_8": 5,
    "SMARCC2-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "SMARCC2-related_disorder|not_specified|Inborn_genetic_diseases|Coffin-Siris_syndrome_8": 1,
    "SMARCC2-related_neurodevelopmental_disorder": 2,
    "Coffin-Siris_syndrome_8|not_provided": 5,
    "not_provided|SMARCC2-related_disorder": 3,
    "Coffin-Siris_syndrome_8|SMARCC2-related_disorder": 1,
    "SMARCC2-related_BAFopathy|Coffin-Siris_syndrome_8|SMARCC2-related_disorder": 1,
    "SMARCC2-related_BAFopathy": 3,
    "Coffin-Siris_syndrome_8|not_specified": 1,
    "Inborn_genetic_diseases|Generalized_hypotonia": 1,
    "Coffin-Siris_syndrome_8|Intellectual_disability": 1,
    "SMARCC2-related_disorder|not_provided": 1,
    "not_provided|Myopia_24|_autosomal_dominant": 2,
    "Myopia_24|_autosomal_dominant": 8,
    "not_provided|SLC39A5-related_disorder": 2,
    "SLC39A5-related_disorder": 5,
    "SLC39A5-related_disorder|not_provided": 1,
    "not_specified|Myopia_24|_autosomal_dominant": 2,
    "not_provided|SLC39A5-related_disorder|Myopia_24|_autosomal_dominant": 1,
    "Abnormality_of_the_face|Craniosynostosis_syndrome": 1,
    "PAN2-related_multiple_congenital_anomalies_syndrome": 3,
    "PAN2-related_disorder": 2,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 415,
    "Inborn_genetic_diseases|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 20,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|STAT2-related_disorder": 4,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|STAT2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 3,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|not_provided": 6,
    "STAT2-related_disorder|not_provided|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 1,
    "STAT2-related_disorder|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|not_provided": 1,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 4,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|Pseudo-TORCH_syndrome_3": 1,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|Inborn_genetic_diseases": 8,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|not_specified|not_provided": 1,
    "Susceptibility_to_severe_COVID-19|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|not_provided": 1,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|not_provided|not_specified": 1,
    "Pseudo-TORCH_syndrome_3|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 2,
    "Pseudo-TORCH_syndrome_3": 2,
    "not_provided|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|STAT2-related_disorder|not_specified": 1,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|not_provided|STAT2-related_disorder": 1,
    "not_provided|STAT2-related_disorder|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 1,
    "not_provided|Susceptibility_to_severe_COVID-19|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 1,
    "not_specified|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection": 1,
    "Inborn_genetic_diseases|Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|Pseudo-TORCH_syndrome_3": 1,
    "Advanced_sleep_phase_syndrome|_familial|_4": 1,
    "Advance_sleep_phase_syndrome|_familial|_4": 2,
    "Cataract_15_multiple_types": 45,
    "not_provided|Cataract": 3,
    "not_provided|Cataract_15_multiple_types": 9,
    "Inborn_genetic_diseases|Cataract_15_multiple_types": 4,
    "MIP-related_disorder|Inborn_genetic_diseases|Cataract_15_multiple_types|not_provided": 1,
    "MIP-related_disorder": 2,
    "Developmental_cataract|Microphthalmia|Nystagmus|Microcornea": 1,
    "Developmental_cataract|Cataract_15_multiple_types": 1,
    "Cataract_15_multiple_types|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Cataract_15_multiple_types": 1,
    "Cataract_15_multiple_types|not_provided": 1,
    "Persistent_hyperplastic_primary_vitreous|Cataract_15_multiple_types|Developmental_cataract": 1,
    "Hypermetabolism_due_to_uncoupled_mitochondrial_oxidative_phosphorylation_2|Hypermetabolism_due_to_Defect_in_Mitochondrial_Coupling": 1,
    "Primordial_dwarfism-immunodeficiency-lipodystrophy_syndrome|Microcephalic_primordial_dwarfism": 3,
    "Lamellar_ichthyosis|Ichthyosis_and_erythrokeratoderma": 1,
    "not_provided|Ichthyosis|_congenital|_autosomal_recessive_13|Congenital_ichthyosis_of_skin": 1,
    "SDR9C7-related_disorder|not_provided|Ichthyosis|_congenital|_autosomal_recessive_13|Lamellar_ichthyosis": 1,
    "Ichthyosis|_congenital|_autosomal_recessive_13|Ichthyosis_and_erythrokeratoderma|Lamellar_ichthyosis|not_provided": 1,
    "Ichthyosis|_congenital|_autosomal_recessive_13|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Ichthyosis|_congenital|_autosomal_recessive_13|Lamellar_ichthyosis": 1,
    "Lamellar_ichthyosis|Congenital_ichthyosis_of_skin": 1,
    "SDR9C7-related_disorder": 1,
    "SDR9C7-related_disorder|not_specified|not_provided": 1,
    "Ichthyosis|_congenital|_autosomal_recessive_13": 1,
    "Intellectual_disability|_autosomal_recessive_53|Lamellar_ichthyosis|Congenital_ichthyosis_of_skin|Ichthyosis|_congenital|_autosomal_recessive_13": 1,
    "ZBTB39-related_condition": 1,
    "not_provided|HYPOGONADOTROPIC_HYPOGONADISM_10_WITHOUT_ANOSMIA": 1,
    "Infertility_disorder|not_provided|Delayed_puberty": 1,
    "Hypogonadotropic_hypogonadism_10_with_or_without_anosmia": 2,
    "Delayed_puberty|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "TAC3-related_disorder": 2,
    "not_specified|Hypogonadotropic_hypogonadism_10_with_or_without_anosmia": 1,
    "not_specified|MYO1A-related_disorder": 2,
    "not_provided|MYO1A-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_48": 5,
    "not_specified|not_provided|MYO1A-related_disorder": 1,
    "MYO1A-related_disorder": 3,
    "not_specified|not_provided|Diarrhea_15|_congenital|Congenital_diarrhea": 1,
    "MYO1A-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_48": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_48|not_specified|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_48|MYO1A-related_disorder|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_48": 1,
    "Diarrhea_15|_congenital|Congenital_diarrhea": 1,
    "not_specified|Nonsyndromic_Hearing_Loss|_Dominant|MYO1A-related_disorder": 1,
    "MYO1A-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_48": 1,
    "MYO1A-related_disorder|not_specified|not_provided": 1,
    "Hyper-IgE_syndrome_6|_autosomal_dominant|_with_recurrent_infections": 6,
    "LRP1-related_disorder": 47,
    "Keratosis_pilaris_atrophicans|not_specified|not_provided|Developmental_dysplasia_of_the_hip_3|LRP1-related_disorder|Keratosis_pilaris": 1,
    "Keratosis_pilaris_atrophicans|Developmental_dysplasia_of_the_hip_3": 2,
    "Developmental_dysplasia_of_the_hip_3": 4,
    "not_provided|LRP1-related_disorder": 5,
    "not_provided|not_specified|LRP1-related_disorder": 1,
    "Developmental_dysplasia_of_the_hip_3|Keratosis_pilaris_atrophicans": 1,
    "Ventricular_septal_defect|Tricuspid_atresia": 2,
    "LRP1-related_disorder|not_provided": 11,
    "Keratosis_pilaris|not_provided": 7,
    "Keratosis_pilaris|Atrophoderma_vermiculatum": 1,
    "not_provided|Keratosis_pilaris": 5,
    "Keratosis_pilaris_atrophicans": 2,
    "Developmental_disorder|Variant_of_unknown_significance": 1,
    "Neurodevelopmental_disorder_with_cardiomyopathy|_spasticity|_and_brain_abnormalities": 9,
    "SHMT2-related_disorder": 2,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_cardiomyopathy|_spasticity|_and_brain_abnormalities": 2,
    "not_provided|Neurodevelopmental_disorder_with_cardiomyopathy|_spasticity|_and_brain_abnormalities": 1,
    "SHMT2-related_disorder|Neurodevelopmental_disorder_with_cardiomyopathy|_spasticity|_and_brain_abnormalities": 1,
    "SHMT2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_cardiomyopathy|_spasticity|_and_brain_abnormalities": 1,
    "Inborn_genetic_diseases|Bailey-Bloch_congenital_myopathy": 9,
    "not_provided|Bailey-Bloch_congenital_myopathy|not_specified": 2,
    "Bailey-Bloch_congenital_myopathy": 190,
    "Bailey-Bloch_congenital_myopathy|STAC3-related_disorder|not_specified|not_provided": 1,
    "Bailey-Bloch_congenital_myopathy|Inborn_genetic_diseases": 6,
    "STAC3-related_disorder|Bailey-Bloch_congenital_myopathy": 2,
    "not_specified|not_provided|Bailey-Bloch_congenital_myopathy": 1,
    "Bailey-Bloch_congenital_myopathy|not_provided": 8,
    "Bailey-Bloch_congenital_myopathy|STAC3-related_disorder": 1,
    "Inborn_genetic_diseases|Bailey-Bloch_congenital_myopathy|not_provided": 1,
    "STAC3-related_disorder|Bailey-Bloch_congenital_myopathy|not_provided": 1,
    "not_specified|Bailey-Bloch_congenital_myopathy": 1,
    "not_provided|not_specified|Bailey-Bloch_congenital_myopathy": 2,
    "Bailey-Bloch_congenital_myopathy|not_provided|Inborn_genetic_diseases": 1,
    "Bailey-Bloch_congenital_myopathy|not_specified": 2,
    "not_provided|Bailey-Bloch_congenital_myopathy": 2,
    "Bailey-Bloch_congenital_myopathy|not_specified|not_provided": 1,
    "not_provided|STAC3-related_disorder": 1,
    "not_specified|GLI1-related_disorder": 1,
    "GLI1-related_disorder": 11,
    "not_provided|GLI1-related_disorder": 7,
    "Polydactyly|_postaxial|_type_A8": 6,
    "GLI1-related_disorder|not_provided": 6,
    "Polydactyly_of_a_biphalangeal_thumb|GLI1-related_disorder|not_provided|Polydactyly|_postaxial|_type_A8": 1,
    "not_provided|Polydactyly|_postaxial|_type_A8": 1,
    "not_specified|Polydactyly|_postaxial|_type_A8": 1,
    "GLI1-related_disorder|not_specified": 1,
    "Polydactyly_of_a_biphalangeal_thumb|Polydactyly|_postaxial|_type_A8": 1,
    "Polydactyly|_postaxial|_type_A8|Polydactyly_of_a_biphalangeal_thumb|GLI1-related_disorder|not_provided": 1,
    "not_provided|Polydactyly|_postaxial|_type_A8|Polydactyly_of_a_biphalangeal_thumb": 1,
    "Coronary_artery_spasm_3|_susceptibility_to": 1,
    "not_provided|Hereditary_spastic_paraplegia|not_specified": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 334,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 177,
    "Spastic_paraplegia_70|_autosomal_recessive|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_provided": 7,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_provided": 8,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_specified": 16,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified": 37,
    "not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 30,
    "not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified": 4,
    "not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 6,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Charcot-Marie-Tooth_disease": 8,
    "not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease|not_specified": 6,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|See_cases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 2,
    "MARS1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_provided": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 7,
    "not_specified|not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 3,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease|not_provided": 2,
    "not_specified|MARS1-related_disorder|not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_provided|MARS1-related_disorder": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2U": 5,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|MARS1-related_disorder|not_specified|not_provided": 2,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 11,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_specified|MARS1-related_disorder": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|Distal_spinal_muscular_atrophy": 1,
    "not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_provided|Charcot-Marie-Tooth_disease": 3,
    "MARS1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|not_provided": 3,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_specified": 4,
    "not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|MARS1-related_disorder": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|MARS1-related_disorder": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_specified|MARS1-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_specified|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Trichothiodystrophy_9|_nonphotosensitive|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 2,
    "not_specified|Charcot-Marie-Tooth_disease|not_provided|MARS-related_disorder|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_provided": 3,
    "MARS1-related_disorder|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 2,
    "Spastic_paraplegia_70|_autosomal_recessive": 1,
    "not_provided|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|MARS1-related_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Trichothiodystrophy_9|_nonphotosensitive": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|MARS1-related_disorder|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Trichothiodystrophy_9|_nonphotosensitive": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "not_specified|MARS1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 1,
    "MARS-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_provided": 1,
    "MARS1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|MARS1-related_disorder|not_provided|Charcot-Marie-Tooth_disease": 1,
    "MARS1-related_disorder|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified": 1,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_provided": 2,
    "Pulmonary_alveolar_proteinosis|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Spastic_paraplegia_70|_autosomal_recessive|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Spastic_paraplegia_70|_autosomal_recessive|not_provided|not_specified|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_provided|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|MARS1-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|MARS1-related_disorder|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease": 4,
    "Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|Trichothiodystrophy_9|_nonphotosensitive|not_specified|not_provided": 1,
    "MARS1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2U|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency": 1,
    "MARS1-related_disorder|Severe_early-onset_pulmonary_alveolar_proteinosis_due_to_MARS_deficiency|Charcot-Marie-Tooth_disease_axonal_type_2U|not_specified|not_provided": 1,
    "MBD6-related_disorder": 10,
    "MBD6-related_disorder|not_provided": 3,
    "not_provided|MBD6-related_disorder": 1,
    "not_specified|MBD6-related_disorder": 1,
    "Hereditary_spastic_paraplegia_10": 48,
    "KIF5A-related_disorder": 15,
    "Spastic_paraplegia|KIF5A-related_disorder": 8,
    "Hereditary_spastic_paraplegia_10|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_10|Spastic_paraplegia|KIF5A-related_disorder|not_provided": 1,
    "not_provided|KIF5A-related_disorder|Spastic_paraplegia": 2,
    "KIF5A-related_disorder|Spastic_paraplegia": 14,
    "Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 16,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_10": 9,
    "KIF5A-related_disorder|not_provided|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_10|not_specified": 1,
    "Spastic_Paraglegia_10": 2,
    "Myoclonus|_intractable|_neonatal|Hereditary_spastic_paraplegia_10|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|KIF5A-related_disorder|Hereditary_spastic_paraplegia_10": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder": 1,
    "KIF5A-related_disorder|not_specified|Spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Myoclonus|_intractable|_neonatal|Hereditary_spastic_paraplegia_10": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "Myoclonus|_intractable|_neonatal|Hereditary_spastic_paraplegia_10": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_10|Hereditary_spastic_paraplegia": 1,
    "Myoclonus|_intractable|_neonatal|Spastic_paraplegia|KIF5A-related_disorder|not_provided|Hereditary_spastic_paraplegia_10": 1,
    "Myoclonus|_intractable|_neonatal": 11,
    "Inherited_neurodegenerative_disorder": 1,
    "Hereditary_spastic_paraplegia_10|not_provided": 2,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_10|Myoclonus|_intractable|_neonatal|not_provided": 1,
    "Hereditary_spastic_paraplegia_10|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Myoclonus|_intractable|_neonatal|Spastic_paraplegia": 2,
    "KIF5A-related_disorder|Hereditary_spastic_paraplegia_10|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Hereditary_spastic_paraplegia_10|Spastic_paraplegia|Demyelinating_peripheral_neuropathy|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|not_provided": 1,
    "Spastic_paraplegia|Myoclonus|_intractable|_neonatal|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2_due_to_KIF5A_mutation|Hereditary_spastic_paraplegia_10": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia|Myoclonus|_intractable|_neonatal|not_specified": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|KIF5A-related_disorder": 1,
    "KIF5A-related_disorder|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_10": 1,
    "KIF5A-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "KIF5A-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_10|not_specified": 1,
    "Myoclonus|_intractable|_neonatal|Spastic_paraplegia": 1,
    "KIF5A-related_disorder|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|not_provided|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Intellectual_disability": 1,
    "not_specified|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder|not_provided": 1,
    "KIF5A-related_intractable_neonatal_myoclonus|Spastic_paraplegia": 1,
    "KIF5A-related_disorder|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_10": 2,
    "not_provided|Spastic_paraplegia|KIF5A-related_disorder|Hereditary_spastic_paraplegia_10": 1,
    "Demyelinating_peripheral_neuropathy": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_10": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis|KIF5A-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|KIF5A-related_disorder|Hereditary_spastic_paraplegia_10": 1,
    "Hereditary_spastic_paraplegia_10|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Myoclonus|_intractable|_neonatal|KIF5A-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_specified": 2,
    "Hereditary_spastic_paraplegia_10|Spastic_paraplegia|not_provided|not_specified": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder|not_provided": 1,
    "KIF5A-related_disorder|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Inborn_genetic_diseases|not_provided|KIF5A-related_disorder|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia": 3,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder": 1,
    "Prostate_cancer|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_10|Spastic_paraplegia|Myoclonus|_intractable|_neonatal": 1,
    "Hereditary_spastic_paraplegia_10|KIF5A-related_disorder|Inborn_genetic_diseases|not_provided|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|KIF5A-related_disorder|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|not_provided|Spastic_paraplegia": 1,
    "KIF5A-related_amyotrophic_lateral_sclerosis|Spastic_paraplegia": 1,
    "Myoclonus|_intractable|_neonatal|not_provided": 1,
    "Spastic_paraplegia|Paroxysmal_dyskinesia": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Myoclonus|_intractable|_neonatal|Hereditary_spastic_paraplegia_10|Inborn_genetic_diseases|Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_10|not_specified": 1,
    "Spastic_paraplegia|KIF5A-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_10": 1,
    "Distal_myopathy|not_provided|Hereditary_spastic_paraplegia_10|KIF5A-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_10|Amyotrophic_lateral_sclerosis": 1,
    "not_provided|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Myoclonus|_intractable|_neonatal|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Hereditary_spastic_paraplegia_10": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia_10": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_10|not_provided": 1,
    "Hereditary_spastic_paraplegia|KIF5A-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis|_susceptibility_to|_25": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Hereditary_spastic_paraplegia_10|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25": 1,
    "Hereditary_spastic_paraplegia_10|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25": 1,
    "Hereditary_spastic_paraplegia_10|Myoclonus|_intractable|_neonatal|Amyotrophic_lateral_sclerosis|_susceptibility_to|_25|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_10": 1,
    "not_provided|Hereditary_spastic_paraplegia_10": 3,
    "not_specified|B4GALNT1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_26|not_provided": 1,
    "Hereditary_spastic_paraplegia_26|Spastic_paraparesis": 1,
    "Hereditary_spastic_paraplegia_26": 7,
    "not_provided|B4GALNT1-related_disorder|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_26|not_provided": 2,
    "B4GALNT1-related_disorder|Spastic_paraplegia|not_specified|not_provided": 1,
    "B4GALNT1-related_disorder|not_specified|not_provided|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_26": 1,
    "B4GALNT1-related_disorder": 2,
    "not_provided|Hereditary_spastic_paraplegia_26|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_26": 1,
    "Spastic_paraplegia|not_provided|B4GALNT1-related_disorder": 1,
    "B4GALNT1-related_disorder|not_provided|Spastic_paraplegia": 1,
    "Spastic_paraplegia|B4GALNT1-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia_26": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_26": 1,
    "B4GALNT1-related_disorder|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_26|Spastic_paraplegia": 3,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_26": 1,
    "AGAP2-related_disorder": 15,
    "not_provided|AGAP2-related_disorder": 1,
    "Cutaneous_Malignant_Melanoma|_Dominant|not_provided": 2,
    "Cutaneous_Malignant_Melanoma|_Dominant": 3,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 96,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided": 5,
    "CDK4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 34,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 15,
    "Hereditary_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified|not_provided": 1,
    "CDK4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma": 12,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 14,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 15,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_melanoma": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 18,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 18,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma": 31,
    "Familial_melanoma|not_provided|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|CDK4-related_disorder": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 22,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CDK4-related_disorder|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Familial_melanoma|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma|not_provided": 1,
    "CDK4-related_disorder|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ewing_sarcoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 2,
    "CDK4-related_disorder|Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "not_provided|CDK4-related_disorder|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|not_provided": 2,
    "Familial_melanoma|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 3,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 2,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 2,
    "Familial_melanoma|CDK4-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|not_specified": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 2,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_specified": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|CDK4-related_disorder|Familial_melanoma|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|CDK4-related_disorder": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|not_specified": 3,
    "CDK4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided": 1,
    "CDK4-related_disorder|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 12,
    "Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|CDK4-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|not_provided|CDK4-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Familial_melanoma": 1,
    "Hereditary_cancer-predisposing_syndrome|CDK4-related_disorder|not_provided|not_specified|Familial_melanoma": 1,
    "Familial_melanoma|not_provided|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "not_specified|Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|CDK4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_melanoma|not_specified": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|CDK4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma|not_provided": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma": 1,
    "Familial_melanoma|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|CDK4-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|CDK4-related_disorder|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_melanoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|CDK4-related_disorder": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|CDK4-related_disorder|Familial_melanoma|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|Familial_melanoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_specified|Familial_melanoma": 1,
    "Familial_melanoma|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_3": 2,
    "Vitamin_D-dependent_rickets|_type_1": 22,
    "not_specified|not_provided|Vitamin_D-dependent_rickets|_type_1": 1,
    "Vitamin_D-dependent_rickets|_type_1A|not_provided": 27,
    "Vitamin_D-dependent_rickets|_type_1A": 67,
    "not_provided|Vitamin_D-dependent_rickets|_type_1A": 13,
    "not_specified|Vitamin_D-dependent_rickets|_type_1A": 1,
    "Vitamin_D-dependent_rickets|_type_1|not_provided": 3,
    "not_provided|Vitamin_D-dependent_rickets|_type_1A|CYP27B1-related_disorder": 1,
    "not_provided|Vitamin_D-dependent_rickets|_type_1A|Vitamin_D-dependent_rickets|_type_1|Multiple_sclerosis|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Vitamin_D-dependent_rickets|_type_1A|CYP27B1-related_disorder|not_provided|Vitamin_D-dependent_rickets|_type_1": 1,
    "Inborn_genetic_diseases|Vitamin_D-dependent_rickets|_type_1A": 4,
    "Vitamin_D-dependent_rickets|_type_1A|Inborn_genetic_diseases": 3,
    "not_provided|Vitamin_D-dependent_rickets|_type_1A|Multiple_sclerosis|_susceptibility_to": 1,
    "Vitamin_D-dependent_rickets|_type_1|CYP27B1-related_disorder|Vitamin_D-dependent_rickets|_type_1A|not_provided": 1,
    "Vitamin_D-dependent_rickets|_type_1|not_provided|Vitamin_D-dependent_rickets|_type_1A": 1,
    "Vitamin_D-dependent_rickets|_type_1A|Inborn_genetic_diseases|not_provided": 4,
    "CYP27B1-related_disorder|not_specified|Vitamin_D-dependent_rickets|_type_1A|not_provided|Vitamin_D-dependent_rickets|_type_1": 1,
    "Inborn_genetic_diseases|Vitamin_D-dependent_rickets|_type_1A|not_provided": 1,
    "not_provided|Vitamin_D-dependent_rickets|_type_1": 6,
    "Vitamin_D-dependent_rickets|_type_1A|CYP27B1-related_disorder|not_provided": 2,
    "not_provided|Vitamin_D-dependent_rickets|_type_1A|Inborn_genetic_diseases": 3,
    "Vitamin_D-dependent_rickets|_type_1A|not_provided|Vitamin_D-dependent_rickets|_type_1|Inborn_genetic_diseases": 1,
    "Vitamin_D-dependent_rickets|_type_1A|not_provided|Vitamin_D-dependent_rickets|_type_1": 2,
    "Vitamin_D-dependent_rickets|_type_1A|Vitamin_D-dependent_rickets|_type_1": 2,
    "CYP27B1-related_disorder|not_provided": 1,
    "Vitamin_D-dependent_rickets|_type_1|Vitamin_D-dependent_rickets|_type_1A": 1,
    "not_provided|CYP27B1-related_disorder|Vitamin_D-dependent_rickets|_type_1A": 1,
    "Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3": 63,
    "not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3": 32,
    "Skeletal_myopathy": 1,
    "Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|not_provided": 19,
    "not_specified|not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3": 1,
    "not_provided|Encephalomyopathy_with_respiratory_failure_and_lactic_acidosis|Inborn_genetic_diseases": 1,
    "TSFM-related_disorder|not_provided": 2,
    "not_specified|not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|TSFM-related_disorder": 1,
    "not_specified|not_provided|TSFM-related_disorder": 1,
    "not_provided|not_specified|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3": 1,
    "not_provided|Inborn_genetic_diseases|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3": 2,
    "Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|not_specified|not_provided": 1,
    "TSFM-related_disorder": 2,
    "Inborn_genetic_diseases|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|not_provided": 1,
    "not_provided|TSFM-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_21|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|not_provided": 1,
    "Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|See_cases|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|TSFM-related_disorder|not_specified": 1,
    "Encephalomyopathy_with_respiratory_failure_and_lactic_acidosis|not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|TSFM-related_disorder": 1,
    "not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|Inborn_genetic_diseases": 2,
    "TSFM-related_disorder|not_specified|not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3": 1,
    "not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|TSFM-related_disorder": 2,
    "not_provided|Fatal_mitochondrial_disease_due_to_combined_oxidative_phosphorylation_defect_type_3|Primary_dilated_cardiomyopathy": 1,
    "AVIL-related_disorder": 13,
    "Nephrotic_syndrome|_type_21": 10,
    "Steroid-resistant_nephrotic_syndrome|Nephrotic_syndrome|_type_21": 1,
    "Nephrotic_syndrome|_type_21|Steroid-resistant_nephrotic_syndrome": 3,
    "not_specified|AVIL-related_disorder": 1,
    "not_provided|Nephrotic_syndrome|_type_21": 1,
    "Nephrotic_syndrome|_type_21|Nephrotic_syndrome": 1,
    "CTDSP2-related_disorder": 3,
    "USP15-related_disorder": 9,
    "not_specified|USP15-related_disorder": 2,
    "AVPR1A-related_disorder": 2,
    "Spermatogenic_failure_9|not_provided": 1,
    "Spermatogenic_failure_9": 8,
    "RXYLT1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10": 10,
    "not_provided|RXYLT1-related_disorder": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|not_provided": 2,
    "not_specified|RXYLT1-related_disorder|not_provided": 2,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10": 9,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10": 1,
    "not_specified|not_provided|RXYLT1-related_disorder": 1,
    "not_provided|not_specified|RXYLT1-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|Inborn_genetic_diseases": 1,
    "RXYLT1-related_disorder|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|not_specified|not_provided": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|not_specified": 1,
    "SRGAP1-related_disorder": 13,
    "Thyroid_cancer|_nonmedullary|_2|not_specified": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Nephronophthisis": 1,
    "not_provided|SRGAP1-related_disorder": 3,
    "SRGAP1-related_disorder|not_provided": 2,
    "Thyroid_cancer|_nonmedullary|_2|SRGAP1-related_disorder": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Congenital_anomalies_of_kidney_and_urinary_tract_1": 1,
    "Thyroid_cancer|_nonmedullary|_2|not_provided": 1,
    "not_specified|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "SRGAP1-related_disorder|not_specified": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_83": 5,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 301,
    "TBK1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided": 2,
    "not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 3,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Glaucoma_1|_open_angle|_P": 1,
    "TBK1-related_disorder": 18,
    "TBK1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 17,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 13,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided": 11,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|TBK1-related_disorder": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder": 9,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder": 5,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Glaucoma_1|_open_angle|_P|not_specified|not_provided": 1,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Motor_neuron_disease": 1,
    "not_specified|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Autoinflammation_with_arthritis_and_vasculitis|Motor_neuron_disease|TBK1-related_disorder": 1,
    "not_provided|TBK1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8": 3,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided|TBK1-related_disorder": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Glaucoma_1|_open_angle|_P|not_specified": 1,
    "not_provided|TBK1-related_disorder": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder|not_provided": 3,
    "Autoinflammation_with_arthritis_and_vasculitis": 2,
    "TBK1-related_disorder|Amyotrophic_lateral_sclerosis|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Autoinflammation_with_arthritis_and_vasculitis|TBK1-related_disorder": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Motor_neuron_disease|not_provided": 1,
    "TBK1-related_disorder|Spastic_hemiparesis|Progressive_spasticity|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder|not_specified": 1,
    "Glaucoma_1|_open_angle|_P|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_specified": 2,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Amyotrophic_lateral_sclerosis": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|See_cases": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Motor_neuron_disease": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8": 1,
    "not_specified|TBK1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "TBK1-related_disorder|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 2,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 3,
    "Autoinflammation_with_arthritis_and_vasculitis|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided|Motor_neuron_disease": 1,
    "Incidental_Discovery|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder|Primary_open_angle_glaucoma|Herpes_simplex_encephalitis|_susceptibility_to|_1|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder|Inborn_genetic_diseases": 1,
    "Severe_SARS-CoV-2_infection|_susceptibility_to|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided": 1,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|TBK1-related_disorder|Susceptibility_to_severe_COVID-19": 1,
    "Amyotrophic_lateral_sclerosis|TBK1-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|Inborn_genetic_diseases": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided|TBK1-related_disorder|Autoinflammation_with_arthritis_and_vasculitis|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_8": 1,
    "Glaucoma_1|_open_angle|_P|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4": 1,
    "Primary_progressive_non_fluent_aphasia|Corticobasal_syndrome": 1,
    "not_specified|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_4|not_provided": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-D": 14,
    "Mucopolysaccharidosis|_MPS-III-D": 624,
    "Mucopolysaccharidosis|_MPS-III-D|not_provided": 7,
    "Mucopolysaccharidosis|_MPS-III-D|Sanfilippo_syndrome": 18,
    "Mucopolysaccharidosis|_MPS-III-D|not_specified": 2,
    "Mucopolysaccharidosis|_MPS-III-D|not_provided|GNS-related_disorder|Sanfilippo_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-D": 11,
    "Mucopolysaccharidosis|_MPS-III-D|not_provided|not_specified|Sanfilippo_syndrome": 1,
    "Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-D": 12,
    "Mucopolysaccharidosis|_MPS-III-D|Inborn_genetic_diseases": 13,
    "GNS-related_disorder|Mucopolysaccharidosis|_MPS-III-D": 4,
    "Mucopolysaccharidosis|_MPS-III-D|not_provided|Sanfilippo_syndrome": 2,
    "Sanfilippo_syndrome|not_provided|Mucopolysaccharidosis|_MPS-III-D": 1,
    "Mucopolysaccharidosis|_MPS-III-D|Inborn_genetic_diseases|not_provided": 1,
    "GNS-related_disorder": 1,
    "GNS-related_disorder|Mucopolysaccharidosis|_MPS-III-D|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-D|Sanfilippo_syndrome|GNS-related_disorder": 1,
    "not_provided|Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-D": 1,
    "Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-D|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis|_MPS-III-D": 1,
    "Mucopolysaccharidosis|_MPS-III-D|GNS-related_disorder|Sanfilippo_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-III-D|not_specified|not_provided": 1,
    "Sanfilippo_syndrome|not_specified|Mucopolysaccharidosis|_MPS-III-D|not_provided": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-D": 1,
    "not_specified|not_provided|Mucopolysaccharidosis|_MPS-III-D|Sanfilippo_syndrome": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-D|Sanfilippo_syndrome|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-III-D|Sanfilippo_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Sanfilippo_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-D": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-D|not_provided|Sanfilippo_syndrome|GNS-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-III-D|Inborn_genetic_diseases|Sanfilippo_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-III-D|not_specified|GNS-related_disorder|Sanfilippo_syndrome|not_provided": 1,
    "Dermatofibrosis_lenticularis_disseminata": 54,
    "not_provided|Dermatofibrosis_lenticularis_disseminata": 33,
    "Inborn_genetic_diseases|LEMD3-related_disorder|not_provided": 1,
    "LEMD3-related_disorder|OSTEOPOIKILOSIS_WITH_OR_WITHOUT_MELORHEOSTOSIS|Dermatofibrosis_lenticularis_disseminata|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Dermatofibrosis_lenticularis_disseminata": 5,
    "LEMD3-related_disorder|not_provided": 5,
    "not_provided|not_specified|Dermatofibrosis_lenticularis_disseminata": 3,
    "LEMD3-related_disorder": 2,
    "Osteopoikilosis": 1,
    "Inborn_genetic_diseases|not_provided|Dermatofibrosis_lenticularis_disseminata": 2,
    "not_provided|LEMD3-related_disorder": 3,
    "not_provided|LEMD3-related_disorder|Inborn_genetic_diseases|Dermatofibrosis_lenticularis_disseminata": 1,
    "Dermatofibrosis_lenticularis_disseminata|not_provided": 3,
    "Dermatofibrosis_lenticularis_disseminata|_isolated": 1,
    "Gorham-Stout_disease": 1,
    "not_specified|not_provided|Dermatofibrosis_lenticularis_disseminata": 1,
    "Melorheostosis_with_osteopoikilosis|not_provided": 1,
    "Melorheostosis_with_osteopoikilosis|Dermatofibrosis_lenticularis_disseminata|_isolated|not_provided": 1,
    "Osteopoikilosis|Dermatofibrosis_lenticularis_disseminata": 1,
    "not_provided|Dermatofibrosis_lenticularis_disseminata|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_74": 10,
    "not_specified|not_provided|MSRB3-related_disorder": 1,
    "MSRB3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_74": 1,
    "MSRB3-related_disorder|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_74|Hearing_loss|_autosomal_recessive": 1,
    "Hearing_loss|Rare_genetic_deafness": 1,
    "not_provided|MSRB3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_74": 1,
    "HMGA2-related_disorder": 4,
    "Silver-Russell_syndrome_5": 8,
    "Silver-Russell_syndrome_5|Silver-Russell_syndrome_1": 1,
    "Silver-Russell_syndrome_5|Silver-Russell_syndrome_1|not_provided": 1,
    "Silver-Russell_syndrome_5|HMGA2-related_disorder|not_provided": 1,
    "HMGA2-related_disorder|not_provided": 2,
    "Uterine_leiomyoma": 27,
    "Silver-Russell_syndrome_5|not_provided": 1,
    "IRAK3-related_disorder": 11,
    "Asthma-related_traits|_susceptibility_to|_5": 2,
    "IRAK3-related_disorder|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_1|not_provided|Multisystem_inflammatory_syndrome_in_children": 1,
    "not_provided|Fraser_syndrome_3": 17,
    "GRIP1-related_disorder": 8,
    "Fraser_syndrome_3|GRIP1-related_disorder": 1,
    "not_provided|GRIP1-related_disorder": 9,
    "Fraser_syndrome_3|Inborn_genetic_diseases": 10,
    "GRIP1-related_disorder|not_provided": 7,
    "Inborn_genetic_diseases|Fraser_syndrome_3": 18,
    "Fraser_syndrome_3|not_provided": 16,
    "Microcephaly|Intellectual_disability|Fraser_syndrome_3|not_provided": 1,
    "not_specified|GRIP1-related_disorder": 1,
    "GRIP1-related_disorder|Fraser_syndrome_3|not_provided": 2,
    "Fraser_syndrome_3|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Fraser_syndrome_3|not_provided": 1,
    "Fraser_syndrome_3|not_specified|not_provided|Intellectual_disability": 2,
    "Fraser_syndrome_1|not_provided|Fraser_syndrome_3|not_specified": 1,
    "GRIP1-related_disorder|not_specified": 1,
    "Fraser_syndrome_3|not_specified|Fraser_syndrome_1|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Fraser_syndrome_3": 1,
    "Fraser_syndrome_3|Fraser_syndrome_1|not_provided|not_specified": 2,
    "not_provided|Fraser_syndrome_3|GRIP1-related_disorder": 2,
    "Fraser_syndrome_3|not_specified|not_provided": 1,
    "Fraser_syndrome_3|GRIP1-related_disorder|not_specified|not_provided": 1,
    "Fraser_syndrome_3|GRIP1-related_disorder|not_provided": 3,
    "not_provided|Fraser_syndrome_3|Inborn_genetic_diseases": 2,
    "Fraser_syndrome_3|not_provided|not_specified": 2,
    "not_provided|Fraser_syndrome_3|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Fraser_syndrome_3": 1,
    "not_specified|not_provided|Fraser_syndrome_3": 1,
    "Fraser_syndrome_3|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Fraser_syndrome_3|Abnormal_brain_morphology": 1,
    "not_provided|Aplastic_anemia": 2,
    "Immunodeficiency_69": 1,
    "Aplastic_anemia|Immunodeficiency_69|Tuberous_sclerosis_2": 1,
    "not_specified|not_provided|Immunodeficiency_69": 1,
    "Tsc2_angiomyolipomas|_renal|_modifier_of|Aplastic_anemia|_susceptibility_to": 1,
    "Mycobacterium_tuberculosis|_protection_against": 1,
    "Acquired_immunodeficiency_syndrome|_rapid_progression_to": 1,
    "Hepatitis_C_virus_infection|_response_to_therapy_of": 1,
    "Neurodevelopmental_disorder|Retinal_disorder": 1,
    "Thrombocytopenia_11_with_multiple_congenital_anomalies_and_dysmorphic_facies": 6,
    "RAP1B-related_disorder": 3,
    "See_cases|Thrombocytopenia_11_with_multiple_congenital_anomalies_and_dysmorphic_facies": 1,
    "NUP107-related_disorder": 16,
    "Premature_ovarian_insufficiency|Inborn_genetic_diseases": 2,
    "Galloway-Mowat_syndrome_7|Nephrotic_syndrome|_type_11|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|NUP107-related_disorder|not_provided": 1,
    "Nephrotic_syndrome|_type_11": 10,
    "Galloway-Mowat_syndrome_7|not_provided|Light_complexion|Early_onset_focal_segmental_glomerulosclerosis|Global_developmental_delay": 1,
    "NUP107-related_disorder|not_provided": 4,
    "NUP107-related_disorder|Nephrotic_syndrome|_type_11|Ovarian_dysgenesis_6|Galloway-Mowat_syndrome_7|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|NUP107-related_disorder": 4,
    "Galloway-Mowat_syndrome_7": 4,
    "Ovarian_dysgenesis_6": 2,
    "NUP107-related_disorder|Nephrotic_syndrome|_type_11": 1,
    "Focal_segmental_glomerulosclerosis_1": 85,
    "not_specified|Galloway-Mowat_syndrome_7|Nephrotic_syndrome|_type_11|not_provided": 1,
    "Accelerated_tumor_formation|_susceptibility_to": 141,
    "not_provided|Accelerated_tumor_formation|_susceptibility_to": 2,
    "Lessel-kubisch_syndrome|Accelerated_tumor_formation|_susceptibility_to": 6,
    "Accelerated_tumor_formation|_susceptibility_to|not_provided": 4,
    "Accelerated_tumor_formation|_susceptibility_to|Lessel-kubisch_syndrome": 4,
    "Accelerated_tumor_formation|_susceptibility_to|not_specified": 6,
    "not_specified|Accelerated_tumor_formation|_susceptibility_to": 7,
    "Accelerated_tumor_formation|_susceptibility_to|not_provided|MDM2-related_condition": 1,
    "Accelerated_tumor_formation|_susceptibility_to|not_specified|Lessel-kubisch_syndrome": 1,
    "not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 9,
    "Amyloidosis|_hereditary_systemic_5": 20,
    "Inborn_genetic_diseases|Amyloidosis|_hereditary_systemic_5": 2,
    "Amyloidosis|_hereditary_systemic_5|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "not_provided|Familial_visceral_amyloidosis|_Ostertag_type|not_specified|Amyloidosis|_hereditary_systemic_5": 1,
    "not_specified|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "Amyloidosis|_hereditary_systemic_5|Inborn_genetic_diseases": 1,
    "not_provided|Familial_visceral_amyloidosis|_Ostertag_type|not_specified": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|not_provided": 6,
    "Dilated_Cardiomyopathy|_Dominant|LRRC10-related_disorder": 1,
    "not_specified|not_provided|Dilated_Cardiomyopathy|_Dominant": 1,
    "CNOT2-related_disorder": 3,
    "Intellectual_developmental_disorder_with_nasal_speech|_dysmorphic_facies|_and_variable_skeletal_anomalies": 4,
    "Intellectual_developmental_disorder_with_nasal_speech|_dysmorphic_facies|_and_variable_skeletal_anomalies|not_provided": 1,
    "not_specified|Intellectual_developmental_disorder_with_nasal_speech|_dysmorphic_facies|_and_variable_skeletal_anomalies": 1,
    "PTPRB-related_disorder": 1,
    "Tryptophan_5-monooxygenase_deficiency": 33,
    "not_provided|Tryptophan_5-monooxygenase_deficiency": 3,
    "Tryptophan_5-monooxygenase_deficiency|not_provided": 4,
    "not_provided|Tryptophan_5-monooxygenase_deficiency|Attention_deficit-hyperactivity_disorder|_susceptibility_to|_7|Major_depressive_disorder": 1,
    "Tryptophan_5-monooxygenase_deficiency|Bipolar_affective_disorder|_susceptibility_to|Attention_deficit-hyperactivity_disorder|_susceptibility_to|_7|Major_depressive_disorder": 1,
    "Major_depressive_disorder|Attention_deficit-hyperactivity_disorder|_susceptibility_to|_7": 1,
    "Unipolar_depression|_susceptibility_to": 1,
    "Long_QT_syndrome_12": 13,
    "KCNC2-related_disorder": 6,
    "Developmental_and_epileptic_encephalopathy|_9": 838,
    "Developmental_and_epileptic_encephalopathy_103": 18,
    "KCNC2-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy_103|not_provided": 1,
    "not_provided|KCNC2-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_103": 1,
    "Bardet-Biedl_syndrome_10": 204,
    "Bardet-Biedl_syndrome_10|not_provided": 6,
    "not_provided|Bardet-Biedl_syndrome_10": 4,
    "BBS10-related_disorder": 40,
    "Bardet-Biedl_syndrome_10|BBS10-related_disorder|Bardet-Biedl_syndrome": 6,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 39,
    "BBS10-related_disorder|Bardet-Biedl_syndrome": 24,
    "BBS10-related_disorder|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 4,
    "Bardet-Biedl_syndrome|BBS10-related_disorder": 26,
    "not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 69,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_10": 2,
    "Inborn_genetic_diseases|not_specified|Bardet-Biedl_syndrome_10|BBS10-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|BBS10-related_disorder|Bardet-Biedl_syndrome_10": 6,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 7,
    "Bardet-Biedl_syndrome|BBS10-related_ciliopathy|BBS10-related_disorder|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|BBS10-related_disorder": 7,
    "Bardet-Biedl_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "BBS10-related_disorder|Inborn_genetic_diseases": 3,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|BBS10-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|BBS10-related_disorder": 3,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_10|BBS10-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_10": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|not_provided": 2,
    "BBS10-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 9,
    "Bardet-Biedl_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_10|BBS10-related_disorder": 2,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|BBS10-related_disorder|Bardet-Biedl_syndrome_10": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|BBS10-related_disorder": 3,
    "not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome_10|BBS10-related_disorder|Bardet-Biedl_syndrome|not_specified": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS10-related_disorder|Bardet-Biedl_syndrome_10": 2,
    "BBS10-related_disorder|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_10": 2,
    "not_specified|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 2,
    "BBS10-related_disorder|Bardet-Biedl_syndrome_10|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|BBS10-related_disorder|Bardet-Biedl_syndrome_10": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|Inborn_genetic_diseases": 1,
    "not_specified|Bardet-Biedl_syndrome_10": 2,
    "Bardet-Biedl_syndrome_10|not_provided|BBS10-related_disorder|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|not_specified|BBS10-related_disorder": 1,
    "Bardet-Biedl_syndrome_10|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "BBS10-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 1,
    "BBS10-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 2,
    "Bardet-Biedl_syndrome_10|BBS10-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|not_provided": 3,
    "not_provided|BBS10-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 2,
    "Inborn_genetic_diseases|BBS10-related_disorder|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|BBS10-related_disorder|not_provided": 1,
    "BBS10-related_disorder|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|not_specified": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10|BBS10-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_10|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_10|not_specified": 3,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|not_specified": 1,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|Asphyxiating_thoracic_dystrophy_3": 1,
    "Bardet-Biedl_syndrome_10|not_specified|Bardet-Biedl_syndrome": 1,
    "BBS10-related_disorder|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome_10|Optic_atrophy": 1,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "not_provided|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|BBS10-related_disorder|Bardet-biedl_syndrome_1/10|_digenic": 1,
    "not_specified|Bardet-Biedl_syndrome|BBS10-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_10|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 4,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_10": 1,
    "BBS10-related_disorder|not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_10": 1,
    "Inborn_genetic_diseases|BBS10-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_10": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_10|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_10|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|BBS10-related_disorder|not_provided": 2,
    "BBS10-related_ciliopathy|BBS10-related_disorder|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_10": 1,
    "BBS10-related_disorder|Bardet-Biedl_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|BBS10-related_disorder|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|BBS10-related_disorder": 1,
    "BBS10-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_1|not_provided": 1,
    "BBS10-related_disorder|Bardet-biedl_syndrome_6/10|_digenic|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_10": 1,
    "Bardet-Biedl_syndrome_10|not_provided|Bardet-Biedl_syndrome|Retinal_dystrophy": 1,
    "not_specified|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|BBS10-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS10-related_disorder": 1,
    "BBS10-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1": 1,
    "Postaxial_hand_polydactyly|Foot_polydactyly|High-frequency_hearing_impairment|Intellectual_disability|Macular_degeneration|Retinal_dystrophy|Inborn_genetic_diseases|BBS10-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_10": 1,
    "BBS10-related_disorder|not_specified|Bardet-Biedl_syndrome_10": 1,
    "Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome_10|Bardet-Biedl_syndrome": 1,
    "Hearing_impairment|Obesity|Sleep_apnea|Cardiac_arrhythmia|Midface_retrusion|Trigonocephaly|Broad_eyebrow": 1,
    "Neurodevelopmental_disorder_with_poor_or_absent_speech|_dysmorphic_facies|_and_behavioral_abnormalities": 4,
    "NAV3-associated_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_poor_or_absent_speech|_dysmorphic_facies|_and_behavioral_abnormalities": 1,
    "SYT1-associated_neurodevelopmental_disorder": 1,
    "Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome": 18,
    "not_provided|SYT1-related_disorder": 1,
    "SYT1-related_disorder": 4,
    "Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome|not_provided|SYT1-related_disorder": 1,
    "SYT1-related_disorder|not_provided": 3,
    "Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome|SYT1-associated_neurodevelopmental_disorder": 3,
    "not_provided|Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome": 1,
    "SYT1-associated_neurodevelopmental_disorder|Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome": 1,
    "SYT1-associated_neurodevelopmental_disorder|Inborn_genetic_diseases|Infantile_hypotonia-oculomotor_anomalies-hyperkinetic_movements-developmental_delay_syndrome|not_provided": 1,
    "PPP1R12A-related_disorder|Genitourinary_and/or_brain_malformation_syndrome": 2,
    "Genitourinary_and/or_brain_malformation_syndrome": 27,
    "PPP1R12A-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Genitourinary_and/or_brain_malformation_syndrome": 1,
    "PPP1R12A-related_disorder": 9,
    "not_provided|PPP1R12A-related_disorder": 2,
    "Genitourinary_and/or_brain_malformation_syndrome|not_provided": 1,
    "PPP1R12A-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84B": 37,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 6,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided": 12,
    "not_provided|OTOGL-related_disorder": 13,
    "OTOGL-related_disorder|not_provided": 13,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_84B|OTOGL-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|OTOGL-related_disorder": 3,
    "not_specified|OTOGL-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided|OTOGL-related_disorder": 1,
    "OTOGL-related_disorder": 11,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 1,
    "OTOGL-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 3,
    "OTOGL-related_disorder|not_specified|not_provided": 9,
    "Meniere_disease|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84B|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided": 1,
    "not_provided|OTOGL-related_disorder|not_specified": 2,
    "Rare_genetic_deafness|See_cases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|OTOGL-related_disorder|not_specified": 1,
    "OTOGL-related_disorder|not_provided|Hearing_impairment|not_specified": 1,
    "OTOGL-related_disorder|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 2,
    "Inborn_genetic_diseases|not_provided|OTOGL-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided": 1,
    "not_specified|not_provided|OTOGL-related_disorder": 4,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_specified|not_provided": 1,
    "OTOGL-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_84B": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84B|Rare_genetic_deafness": 1,
    "not_provided|not_specified|OTOGL-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84B|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|OTOGL-related_disorder|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_dominant_73": 8,
    "PTPRQ-related_disorder|not_provided": 3,
    "not_provided|PTPRQ-related_disorder": 8,
    "PTPRQ-related_disorder": 32,
    "PTPRQ-related_disorder|not_provided|Hearing_loss|_autosomal_recessive|Hearing_impairment": 1,
    "not_provided|PTPRQ-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84A": 34,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84A|not_provided|Hearing_loss|_autosomal_dominant_73": 3,
    "Hearing_loss|_autosomal_dominant_73|Autosomal_recessive_nonsyndromic_hearing_loss_84A|not_provided": 2,
    "not_provided|Hearing_loss|_autosomal_dominant_73|Autosomal_recessive_nonsyndromic_hearing_loss_84A": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84A": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84A|not_provided": 7,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84A|Hearing_loss|_autosomal_dominant_73|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_84A|Hearing_loss|_autosomal_dominant_73": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84A|not_specified|Hearing_loss|_autosomal_dominant_73|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84A|not_specified|not_provided|Hearing_loss|_autosomal_dominant_73": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_84A|Hearing_loss|_autosomal_dominant_73|not_provided": 3,
    "PTPRQ-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_84A": 1,
    "Hearing_loss|_autosomal_dominant_73|not_provided": 2,
    "not_provided|Pain|Unsteady_gait|Pes_planus|Hearing_impairment|Loss_of_ambulation|Pes_cavus|Impaired_vibration_sensation_in_the_lower_limbs": 1,
    "PTPRQ-related_disorder|Hearing_loss|_autosomal_dominant_73|Autosomal_recessive_nonsyndromic_hearing_loss_84A|Hearing_loss|_autosomal_recessive|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_73|Autosomal_recessive_nonsyndromic_hearing_loss_84A": 1,
    "not_provided|Centronuclear_Myopathy|_Dominant": 1,
    "Autosomal_dominant_centronuclear_myopathy|not_specified": 5,
    "Centronuclear_Myopathy|_Dominant": 6,
    "not_specified|Autosomal_dominant_centronuclear_myopathy": 7,
    "Centronuclear_Myopathy|_Dominant|not_provided|Autosomal_dominant_centronuclear_myopathy": 1,
    "not_provided|not_specified|Autosomal_dominant_centronuclear_myopathy": 1,
    "Centronuclear_Myopathy|_Dominant|Autosomal_dominant_centronuclear_myopathy": 1,
    "Autosomal_dominant_centronuclear_myopathy|MYF6-related_disorder|not_provided": 2,
    "Autosomal_dominant_centronuclear_myopathy|not_specified|not_provided": 1,
    "not_specified|Centronuclear_Myopathy|_Dominant": 1,
    "Centronuclear_Myopathy|_Dominant|not_provided": 4,
    "Abnormal_rib_morphology|External_ophthalmoplegia|Scoliosis|Ophthalmoplegia|_external|_with_rib_and_vertebral_anomalies": 1,
    "Ophthalmoplegia|_external|_with_rib_and_vertebral_anomalies": 2,
    "MYF5-related_disorder": 3,
    "MYF5-related_disorder|not_provided": 1,
    "Ophthalmoplegia|_external|_with_rib_and_vertebral_anomalies|External_ophthalmoplegia|Scoliosis|Abnormal_rib_morphology": 1,
    "TMTC2-related_disorder": 2,
    "Frontonasal_dysplasia_-_severe_microphthalmia_-_severe_facial_clefting_syndrome": 4,
    "ALX1-related_disorder|not_provided|not_specified": 1,
    "ALX1-related_disorder|not_specified|not_provided|Frontonasal_dysplasia_-_severe_microphthalmia_-_severe_facial_clefting_syndrome": 1,
    "not_provided|ALX1-related_disorder": 1,
    "ALX1-related_disorder": 1,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4": 7,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5": 2,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|Joubert_syndrome|Leber_congenital_amaurosis|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|not_specified|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 145,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 16,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 140,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 580,
    "CEP290-related_disorder": 111,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 361,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|not_provided": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "CEP290-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 6,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_specified|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|not_provided": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases": 2,
    "CEP290-related_disorder|not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 754,
    "Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 7,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Inborn_genetic_diseases|CEP290-related_disorder": 6,
    "Rod-cone_dystrophy|CEP290-related_ciliopathy|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Retinal_dystrophy|not_provided|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|CEP290-related_disorder|Intellectual_disability": 1,
    "Bardet-Biedl_syndrome_14": 114,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Intellectual_disability": 1,
    "Leber_congenital_amaurosis|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|CEP290-related_ciliopathy|CEP290-related_disorder": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Leber_congenital_amaurosis": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "CEP290-related_disorder|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 20,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Joubert_syndrome_5": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14": 12,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|CEP290-related_disorder": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis|not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 13,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_ciliopathy|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 4,
    "not_provided|Bardet-Biedl_syndrome_14": 2,
    "Bardet-Biedl_syndrome_14|CEP290-related_disorder|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|not_provided|Micrognathia|Abnormal_facial_shape|Global_developmental_delay|Hypotonia|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|CEP290-related_disorder|not_provided": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 8,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 32,
    "not_specified|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 3,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Nephronophthisis": 1,
    "not_provided|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 10,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14": 15,
    "CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 10,
    "Retinal_dystrophy|not_specified|not_provided|Joubert_syndrome_5|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 135,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14": 3,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 3,
    "Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "CEP290-related_disorder|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 11,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 5,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 6,
    "Meckel_syndrome|_type_4|CEP290-related_disorder|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 26,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder": 22,
    "Leber_congenital_amaurosis|CEP290-related_disorder": 5,
    "CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 5,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|CEP290-related_disorder": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder": 2,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Inborn_genetic_diseases|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Retinal_dystrophy|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis|Kidney_disorder|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "not_provided|CEP290-related_ciliopathy|Inborn_genetic_diseases|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_specified": 3,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_ciliopathy|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|not_provided|CEP290-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|not_specified|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_specified": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 2,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5": 2,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 6,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided": 7,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 7,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14": 1,
    "Inborn_genetic_diseases|CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|CEP290-related_disorder|Meckel_syndrome|_type_4": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|CEP290-related_disorder|CEP290-related_ciliopathy|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CEP290-related_disorder|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5": 1,
    "Bardet-Biedl_syndrome_14|CEP290-related_ciliopathy|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Leber_congenital_amaurosis|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 9,
    "Retinal_dystrophy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "CEP290-related_disorder|Intellectual_disability|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "CEP290-related_disorder|Kidney_disorder|not_provided|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 3,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 5,
    "not_provided|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis|Joubert_syndrome_1|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|not_specified": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy": 5,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|not_provided": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 9,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6": 7,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 9,
    "Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 9,
    "not_provided|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10": 2,
    "Inborn_genetic_diseases|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|CEP290-related_disorder|Leber_congenital_amaurosis_10|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|not_provided": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6": 2,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "not_specified|Bardet-Biedl_syndrome_14|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|Leber_congenital_amaurosis|CEP290-related_disorder|not_provided|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|not_provided|See_cases|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 3,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Inborn_genetic_diseases|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 2,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|not_provided|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 2,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 3,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Renal_dysplasia_and_retinal_aplasia|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_10|Inborn_genetic_diseases|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Leber_congenital_amaurosis": 2,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|not_specified": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder": 13,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|CEP290-related_ciliopathy|CEP290-related_disorder|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|Leber_congenital_amaurosis": 1,
    "Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 11,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|not_provided|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Intellectual_disability": 1,
    "Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|not_provided|CEP290-related_disorder": 2,
    "Leber_congenital_amaurosis|CEP290-related_ciliopathy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 1,
    "Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|CEP290-related_disorder|not_specified|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_specified": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 7,
    "Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 4,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_specified|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|CEP290-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "See_cases|Bardet-Biedl_syndrome_14|Joubert_syndrome_1|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 5,
    "not_specified|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Bardet-Biedl_syndrome_14|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis": 3,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 4,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|CEP290-related_disorder": 10,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "Intellectual_disability|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder": 4,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4": 2,
    "not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|CEP290-related_disorder|not_specified": 1,
    "not_provided|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|not_specified|CEP290-related_disorder|not_provided|Leber_congenital_amaurosis|Intellectual_disability": 1,
    "Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided": 1,
    "Joubert_syndrome_5": 11,
    "Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 2,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|not_provided|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Retinal_dystrophy|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 3,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinitis_pigmentosa|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Retinal_dystrophy|not_provided|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|not_provided|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 3,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 3,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|CEP290-related_disorder|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "not_provided|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 4,
    "Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Bardet-Biedl_syndrome_14|not_provided": 2,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|not_provided|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "Joubert_syndrome_5|CEP290-related_disorder": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14": 6,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Bardet-Biedl_syndrome_14": 5,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Retinal_dystrophy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Retinitis_pigmentosa|Joubert_syndrome_1|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|CEP290-related_disorder": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Meckel_syndrome|_type_4|Inborn_genetic_diseases|not_specified|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|CEP290-related_disorder": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14": 2,
    "not_provided|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Occipital_encephalocele|Cystic_renal_dysplasia": 1,
    "not_specified|not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 2,
    "Leber_congenital_amaurosis|not_specified|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4": 2,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_6": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 3,
    "not_provided|CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|CEP290-related_disorder|Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|COG7_congenital_disorder_of_glycosylation|Meckel_syndrome|_type_6|Abnormality_of_the_nervous_system": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|CEP290-related_disorder": 2,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CEP290-related_ciliopathy|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided|Retinitis_pigmentosa": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder": 2,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|not_provided|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 5,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 3,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|not_provided|Leber_congenital_amaurosis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Retinal_dystrophy": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 4,
    "not_specified|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 2,
    "CEP290-related_disorder|not_provided": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|CEP290-related_disorder": 2,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Leber_congenital_amaurosis_10": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder|not_specified": 1,
    "CEP290-related_ciliopathy|CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 5,
    "Meckel_syndrome|_type_4|not_provided|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|not_specified|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Abnormality_of_the_kidney|Polycystic_kidney_disease|Cerebellar_cyst|Cerebellar_vermis_hypoplasia|Hyperechogenic_kidneys": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 4,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|CEP290-related_disorder": 1,
    "CEP290-related_disorder|Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "Stuve-Wiedemann_syndrome_2|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_specified": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Meckel_syndrome|_type_4|CEP290-related_disorder|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|not_provided": 1,
    "CEP290-related_ciliopathy|CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Inborn_genetic_diseases|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "CEP290-related_ciliopathy": 5,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Polycystic_kidney_disease|Encephalocele|Severe_hydrocephalus|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|not_specified|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|not_specified|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "not_provided|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Joubert_syndrome_5|CEP290-related_disorder|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Retinal_dystrophy": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_ciliopathy|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 2,
    "Kidney_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 2,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|CEP290-related_disorder|Leber_congenital_amaurosis|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|not_specified": 1,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis": 2,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Inborn_genetic_diseases|CEP290-related_disorder|not_specified": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Kidney_disorder|Leber_congenital_amaurosis|not_provided|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|not_specified": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|CEP290-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Retinal_dystrophy": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|not_provided|Intellectual_disability|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_4|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 1,
    "not_provided|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 2,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis|not_provided": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided": 5,
    "Meckel_syndrome|_type_4|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 2,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis|not_provided|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 3,
    "Bardet-Biedl_syndrome_14|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder|Leber_congenital_amaurosis|Retinal_dystrophy|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis": 2,
    "Retinitis_pigmentosa|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|CEP290-related_disorder|CEP290-related_ciliopathy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|not_provided": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|CEP290-related_ciliopathy|CEP290-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder": 2,
    "Leber_congenital_amaurosis_10|not_provided": 1,
    "Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 3,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Leber_congenital_amaurosis": 1,
    "not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Cystic_renal_dysplasia|Occipital_encephalocele|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis|Global_developmental_delay|Blindness": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 2,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Retinal_dystrophy|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 3,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "not_provided|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder": 1,
    "CEP290-related_disorder|Retinal_dystrophy|not_provided|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "not_specified|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "Meckel_syndrome|_type_4|not_specified|Leber_congenital_amaurosis|not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|CEP290-related_ciliopathy|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 2,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Leber_congenital_amaurosis|not_provided": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Meckel_syndrome|_type_4|not_specified|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Senior-Loken_syndrome_6|not_provided|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Inborn_genetic_diseases|not_specified|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "not_provided|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Retinal_dystrophy|CEP290-related_ciliopathy|Inborn_genetic_diseases|Leber_congenital_amaurosis|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|CEP290-related_disorder|Blindness|Nystagmus|Central_hypotonia|Molar_tooth_sign_on_MRI|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4": 1,
    "not_provided|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|Meckel_syndrome|_type_6": 1,
    "not_specified|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "not_provided|Leber_congenital_amaurosis|Joubert_syndrome_5|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14": 1,
    "Leber_congenital_amaurosis_10|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Retinitis_pigmentosa": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|not_specified": 2,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Kidney_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy": 2,
    "CEP290-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|not_provided|Leber_congenital_amaurosis|CEP290-related_disorder": 1,
    "not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Optic_atrophy|CEP290-related_disorder|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|not_specified|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided": 1,
    "Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Meckel_syndrome|_type_4|not_specified|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Retinal_dystrophy": 1,
    "Meckel_syndrome|_type_4|not_provided|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Inborn_genetic_diseases": 4,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder": 2,
    "not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 5,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "CEP290-related_ciliopathy|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Retinal_disorder|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|not_provided|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|not_provided": 2,
    "CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Occipital_encephalocele|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Leber_congenital_amaurosis|CEP290-related_disorder": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Leber_congenital_amaurosis|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 7,
    "not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|CEP290-related_disorder": 2,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "CEP290-related_disorder|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Retinal_dystrophy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|CEP290-related_disorder|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided": 1,
    "CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 2,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|Retinal_dystrophy|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Inborn_genetic_diseases|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|not_specified|Joubert_syndrome_5|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Kidney_disorder|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis|not_specified|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|not_provided|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 1,
    "Kidney_disorder|Retinal_dystrophy|not_provided|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|CEP290-related_disorder": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Retinal_dystrophy|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|CEP290-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 2,
    "CEP290-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 8,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|CEP290-related_disorder": 1,
    "not_provided|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 2,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|CEP290-related_ciliopathy|CEP290-related_disorder": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|CEP290-related_disorder": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Leber_congenital_amaurosis|Joubert_syndrome_1|Retinitis_pigmentosa": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|not_provided|Leber_congenital_amaurosis|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis|not_provided|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|not_provided|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Meckel_syndrome|_type_4|Inborn_genetic_diseases|Retinal_dystrophy|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Leber_congenital_amaurosis|Retinitis_pigmentosa|CEP290-related_disorder": 1,
    "CEP290-related_disorder|not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Retinal_dystrophy|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 7,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "CEP290-related_disorder|not_specified|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "not_provided|not_specified|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis|Meckel_syndrome|_type_4": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis_10|Renal_dysplasia_and_retinal_aplasia|Meckel_syndrome|_type_4|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|not_provided|Leber_congenital_amaurosis": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder|not_specified|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder": 2,
    "not_specified|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 2,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|not_provided": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Retinal_dystrophy|CEP290-related_disorder": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|not_provided": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10": 5,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Renal_dysplasia_and_retinal_aplasia|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|not_provided|not_specified|Nephronophthisis|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome|Leber_congenital_amaurosis|Meckel_syndrome|_type_4": 1,
    "Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 6,
    "Leber_congenital_amaurosis|CEP290-related_disorder|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 2,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|not_provided|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Kidney_disorder|Leber_congenital_amaurosis|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|not_specified": 1,
    "Retinal_dystrophy|CEP290-related_ciliopathy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Retinal_dystrophy|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_14|Retinal_dystrophy": 2,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 2,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Inborn_genetic_diseases": 2,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5": 3,
    "Inborn_genetic_diseases|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10": 1,
    "CEP290-related_disorder|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|not_provided|Leber_congenital_amaurosis|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 2,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases": 1,
    "not_provided|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Retinal_dystrophy|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Abnormality_of_the_nervous_system|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|not_provided|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Inborn_genetic_diseases": 1,
    "Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|Bardet-Biedl_syndrome_14": 1,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "not_specified|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Bardet-Biedl_syndrome_14|Polycystic_kidney_disease|Hyperechogenic_kidneys|Cerebellar_cyst|Cerebellar_vermis_hypoplasia|Abnormality_of_the_kidney": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "not_provided|Retinal_dystrophy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "not_specified|CEP290-related_disorder": 2,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_4|not_provided|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|CEP290-related_disorder": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder|Retinal_dystrophy|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|not_provided|Joubert_syndrome_1|Leber_congenital_amaurosis|Retinitis_pigmentosa|Intellectual_disability": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder|Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6": 1,
    "Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Blindness|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Central_hypotonia|Nystagmus|Molar_tooth_sign_on_MRI": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis|CEP290-related_disorder|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Kidney_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_specified": 1,
    "Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|not_specified|not_provided": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|not_provided": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Inborn_genetic_diseases|CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "CEP290-related_disorder|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Retinal_dystrophy|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided|Joubert_syndrome_1|Cone-rod_dystrophy": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Meckel_syndrome|_type_4": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|not_provided": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|CEP290-related_ciliopathy|Meckel_syndrome|_type_4|Kidney_disorder|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|not_specified|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Intellectual_disability|Leber_congenital_amaurosis|Optic_atrophy|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis_10": 1,
    "CEP290-related_disorder|not_specified|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Abnormality_of_prenatal_development_or_birth|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "not_specified|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Leber_congenital_amaurosis|CEP290-related_ciliopathy": 1,
    "CEP20-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "not_specified|Retinal_dystrophy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome_14|Retinal_dystrophy|Joubert_syndrome_1|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|not_specified|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Renal_dysplasia_and_retinal_aplasia|not_specified|not_provided|Leber_congenital_amaurosis|Bardet-Biedl_syndrome|Intellectual_disability": 1,
    "CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|not_specified|CEP290-related_disorder|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|CEP290-related_disorder|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 2,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|Inborn_genetic_diseases|Optic_atrophy": 1,
    "CEP290-related_disorder|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|not_specified": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Inborn_genetic_diseases": 1,
    "not_provided|Joubert_syndrome_5|CEP290-related_disorder|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_14|Retinal_dystrophy": 1,
    "Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|not_specified": 1,
    "CEP290-related_disorder|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis|Retinitis_pigmentosa|not_provided": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "not_provided|Meckel_syndrome|_type_4|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Retinal_dystrophy": 1,
    "Meckel_syndrome|_type_4|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "CEP290-related_disorder|Intellectual_disability|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis|not_provided|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome_14|Retinal_dystrophy|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Retinal_dystrophy|Meckel_syndrome|_type_4|Inborn_genetic_diseases|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Retinal_dystrophy|not_provided": 1,
    "CEP290-related_disorder|not_provided|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Leber_congenital_amaurosis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|not_provided": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10": 1,
    "Meckel_syndrome|_type_4|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "not_provided|Leber_congenital_amaurosis|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|not_specified|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Microcephaly|Retinal_dystrophy|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|CEP290-related_disorder|not_provided": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_5|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Joubert_syndrome_5|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|CEP290-related_ciliopathy|CEP290-related_disorder|not_provided": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Leber_congenital_amaurosis": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|CEP290-related_disorder|not_provided": 2,
    "CEP290-related_disorder|Inborn_genetic_diseases|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "not_specified|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis|Meckel_syndrome|_type_4": 1,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|CEP290-related_disorder|Retinal_dystrophy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome_5|Kidney_disorder|Leber_congenital_amaurosis|not_provided|Retinal_dystrophy|not_specified|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Senior-Loken_syndrome_1": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Inborn_genetic_diseases": 1,
    "not_provided|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|Joubert_syndrome_5|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "not_provided|Retinal_dystrophy|CEP290-related_disorder": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Retinal_dystrophy|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|not_provided|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_14|CEP290-related_disorder": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|CEP290-related_disorder|Retinal_dystrophy|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided": 1,
    "CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|CEP290-related_disorder": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|not_provided|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Retinal_dystrophy": 1,
    "Meckel_syndrome|_type_4|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14": 1,
    "not_specified|CEP290-related_disorder|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis|Joubert_syndrome_1|Abnormality_of_prenatal_development_or_birth": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Retinal_dystrophy|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_1": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis|CEP290-related_disorder": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Kidney_disorder|Leber_congenital_amaurosis|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|not_specified": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome_5": 1,
    "Bardet-Biedl_syndrome_14|not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|not_specified|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_provided|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|not_specified|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Blindness|Global_developmental_delay": 1,
    "CEP290-related_disorder|not_specified": 1,
    "Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Leber_congenital_amaurosis|CEP290-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_specified|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|See_cases|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Kidney_disorder|CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|CEP290-related_disorder": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis|CEP290-related_ciliopathy": 1,
    "CEP290-related_disorder|not_provided|Inborn_genetic_diseases|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder": 1,
    "Bardet-Biedl_syndrome_14|Retinal_dystrophy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_4|Retinal_dystrophy|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|not_specified|Leber_congenital_amaurosis_10": 1,
    "Retinitis_pigmentosa|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_4|not_specified|not_provided|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6": 1,
    "Leber_congenital_amaurosis|CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_provided|CEP290-related_disorder|Leber_congenital_amaurosis|CEP290-related_ciliopathy|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Retinal_dystrophy": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|not_provided|CEP290-related_disorder": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|not_provided": 1,
    "Leber_congenital_amaurosis|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_14|CEP290-related_ciliopathy|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Stuve-Wiedemann_syndrome_2|Inborn_genetic_diseases|Kidney_disorder|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Retinitis_pigmentosa|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis|Joubert_syndrome_1|Atypical_hemolytic-uremic_syndrome|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "not_provided|Leber_congenital_amaurosis|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|CEP290-related_disorder": 2,
    "not_specified|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Intellectual_disability|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_10|Retinal_dystrophy": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|CEP290-related_disorder|Leber_congenital_amaurosis": 1,
    "CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|not_provided": 1,
    "not_specified|CEP290-related_ciliopathies|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 5,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|not_provided|Inborn_genetic_diseases|not_specified|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|not_provided|CEP290-related_disorder": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Meckel_syndrome|_type_4|not_provided|Bardet-Biedl_syndrome|not_specified|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Renal_dysplasia_and_retinal_aplasia|Joubert_syndrome_5|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|not_provided|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|not_provided|not_specified|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Retinal_dystrophy|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|CEP290-related_disorder|not_provided|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis": 1,
    "Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|not_provided": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|not_specified": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|CEP290-related_disorder": 1,
    "not_provided|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "not_provided|CEP290-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|not_provided": 1,
    "Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|not_provided": 1,
    "Encephalocele|Polycystic_kidney_disease|Severe_hydrocephalus|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|not_provided": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5": 1,
    "not_specified|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Intellectual_disability|CEP290-related_disorder|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Retinal_dystrophy|Meckel_syndrome|_type_4|Leber_congenital_amaurosis|not_provided": 1,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|CEP290-related_disorder|Meckel_syndrome|_type_4|Joubert_syndrome_5|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10": 1,
    "Joubert_syndrome_5|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|not_provided|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|not_provided": 1,
    "CEP290-related_ciliopathy|Retinal_dystrophy|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_specified|Joubert_syndrome_5|Leber_congenital_amaurosis|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Retinitis_pigmentosa": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|Leber_congenital_amaurosis|not_provided|CEP290-related_disorder": 1,
    "Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Inborn_genetic_diseases": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Inborn_genetic_diseases|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|not_specified|not_provided": 1,
    "CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 2,
    "CEP290-related_disorder|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6": 1,
    "Renal_dysplasia_and_retinal_aplasia|not_provided|Bardet-Biedl_syndrome|Joubert_syndrome|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Kidney_disorder|Nephronophthisis": 1,
    "Renal_dysplasia_and_retinal_aplasia|Bardet-Biedl_syndrome|Joubert_syndrome|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Nephronophthisis": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_provided": 1,
    "CEP290-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Spastic_ataxia|not_provided|Leber_congenital_amaurosis": 1,
    "Bardet-Biedl_syndrome_14|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder": 1,
    "Retinal_dystrophy|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4": 1,
    "Retinal_dystrophy|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|not_provided": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|CEP290-related_disorder|Leber_congenital_amaurosis|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "Leber_congenital_amaurosis|Senior-Loken_syndrome_6": 1,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_4|CEP290-related_disorder|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6|Retinal_dystrophy|not_provided": 1,
    "not_provided|CEP290-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|not_specified|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis|CEP290-related_ciliopathy|Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome": 1,
    "Night_blindness|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Meckel_syndrome|_type_4|Joubert_syndrome_5|CEP290-related_disorder|CEP290-related_ciliopathy|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Leber_congenital_amaurosis": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|Leber_congenital_amaurosis|not_provided|Meckel_syndrome|_type_4|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10": 1,
    "Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome": 1,
    "CEP290-related_ciliopathy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14": 1,
    "Bardet-Biedl_syndrome_14|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4|Leber_congenital_amaurosis_10": 1,
    "Meckel-Gruber_syndrome|Nephronophthisis|Joubert_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "not_provided|Kidney_disorder|not_specified|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Senior-Loken_syndrome_6|Joubert_syndrome_5|Meckel_syndrome|_type_4": 1,
    "Meckel_syndrome|_type_4|CEP290-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Joubert_syndrome_5|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|CEP290-related_disorder|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Meckel_syndrome|_type_4|not_provided|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Senior-Loken_syndrome_6": 1,
    "Retinal_dystrophy|not_specified|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Retinitis_pigmentosa|Joubert_syndrome_1": 1,
    "not_provided|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5": 1,
    "not_provided|Bardet-Biedl_syndrome_14|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|CEP290-related_disorder": 2,
    "not_provided|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Retinitis_pigmentosa|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Joubert_syndrome_5|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis": 1,
    "CEP290-related_ciliopathy|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis|CEP290-related_disorder|Inborn_genetic_diseases|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis": 1,
    "Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5": 1,
    "CEP290-related_disorder|Joubert_syndrome_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Joubert_syndrome|Nephronophthisis|Meckel-Gruber_syndrome|Leber_congenital_amaurosis|CEP290-related_disorder|Bardet-Biedl_syndrome_14": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|Leber_congenital_amaurosis|Meckel_syndrome|_type_4|Joubert_syndrome_5": 1,
    "Leber_congenital_amaurosis_10|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "CEP290-related_disorder|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|Joubert_syndrome_5|not_provided|Leber_congenital_amaurosis|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis": 1,
    "Leber_congenital_amaurosis|Joubert_syndrome_5|Nephronophthisis|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome|CEP290-related_disorder": 1,
    "Senior-Loken_syndrome_6|Joubert_syndrome_5|Bardet-Biedl_syndrome_14|Leber_congenital_amaurosis_10|Meckel_syndrome|_type_4|not_provided|CEP290-related_disorder|Retinal_dystrophy|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Retinal_dystrophy|Nephronophthisis|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14": 1,
    "CEP290-related_disorder|Meckel_syndrome|_type_4|Joubert_syndrome_5|Leber_congenital_amaurosis_10|Senior-Loken_syndrome_6|Bardet-Biedl_syndrome_14|not_specified": 1,
    "Senior-Loken_syndrome_6|Leber_congenital_amaurosis_10|Bardet-Biedl_syndrome_14|Meckel_syndrome|_type_4|Joubert_syndrome_5": 2,
    "Lissencephaly_8": 13,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_8": 1,
    "Lissencephaly_8|not_provided": 2,
    "not_provided|Lissencephaly_8": 4,
    "not_provided|TMTC3-related_disorder": 5,
    "TMTC3-related_disorder|not_provided": 6,
    "TMTC3-related_disorder": 4,
    "Lissencephaly_8|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_69|not_provided": 1,
    "KITLG-related_disorder": 2,
    "Waardenburg_syndrome|_IIa_2F": 5,
    "KITLG-related_disorder|not_provided": 3,
    "Hyperpigmentation_with_or_without_hypopigmentation|_familial_progressive": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_69": 4,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_69|SKIN/HAIR/EYE_PIGMENTATION_7|_DARK/LIGHT_SKIN|Hyperpigmentation_with_or_without_hypopigmentation|_familial_progressive|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_7|_DARK/LIGHT_SKIN": 2,
    "Hypogonadotropic_hypogonadism_19_with_or_without_anosmia|not_provided": 4,
    "DUSP6-related_disorder|not_provided": 2,
    "DUSP6-related_disorder": 1,
    "not_provided|Hypogonadotropic_hypogonadism_19_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_19_with_or_without_anosmia|not_specified": 1,
    "Hypogonadotropic_hypogonadism_19_with_or_without_anosmia": 1,
    "POC1B-related_disorder|not_provided": 5,
    "Cone-rod_dystrophy_20|not_provided": 20,
    "Cone-rod_dystrophy_20": 33,
    "not_provided|Cone-rod_dystrophy_20": 13,
    "not_provided|Inborn_genetic_diseases|Cone-rod_dystrophy_20": 2,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_20|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_20|not_provided": 3,
    "Cone-rod_dystrophy_20|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy_20": 2,
    "Cone-rod_dystrophy_20|Retinal_dystrophy|not_provided": 1,
    "not_provided|POC1B-related_disorder": 1,
    "Cone-rod_dystrophy_20|Inborn_genetic_diseases|not_provided": 1,
    "Cone-rod_dystrophy_20|not_provided|Retinal_dystrophy": 1,
    "POC1B-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_66": 29,
    "Periventricular_nodular_heterotopia|Isolated_Pierre-Robin_syndrome|Clubfoot|Neurodevelopmental_delay|Hypocalcemia": 2,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_66": 1,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder|_autosomal_dominant_66": 4,
    "ATP2B1-related_disorder": 3,
    "Inborn_genetic_diseases|ATP2B1-related_disorder": 2,
    "Intellectual_developmental_disorder|_autosomal_dominant_66|Neurodevelopmental_disorder": 2,
    "Cornea_plana_2": 11,
    "Cornea_plana_2|not_provided": 2,
    "KERA-related_disorder|not_provided": 1,
    "KERA-related_disorder": 1,
    "not_specified|not_provided|Cornea_plana_2": 1,
    "LUM-related_disorder": 4,
    "LUM-related_disorder|not_provided": 1,
    "Congenital_stromal_corneal_dystrophy": 31,
    "not_provided|Congenital_stromal_corneal_dystrophy": 7,
    "Inborn_genetic_diseases|Congenital_stromal_corneal_dystrophy": 3,
    "DCN-related_disorder": 1,
    "Congenital_stromal_corneal_dystrophy|Inborn_genetic_diseases": 1,
    "Congenital_stromal_corneal_dystrophy|not_provided|DCN-related_disorder": 1,
    "Congenital_stromal_corneal_dystrophy|not_provided": 1,
    "not_provided|Congenital_stromal_corneal_dystrophy|DCN-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_34": 5,
    "Intellectual_disability|_moderate": 3,
    "CRADD-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|not_specified|Intellectual_disability|_autosomal_recessive_34": 1,
    "CRADD-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_34|Inborn_genetic_diseases": 1,
    "CRADD-related_disorder": 2,
    "not_provided|CRADD-related_disorder": 3,
    "not_provided|Intellectual_disability|_autosomal_recessive_34": 1,
    "Intellectual_disability|_autosomal_recessive_34|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_34": 1,
    "not_specified|Intellectual_disability|_autosomal_recessive_34|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_34|not_provided|Seizure|Global_developmental_delay": 1,
    "Intellectual_disability|_autosomal_recessive_34|not_provided|Intellectual_disability": 1,
    "not_specified|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "Nephronophthisis_18": 359,
    "Inborn_genetic_diseases|Nephronophthisis_18": 18,
    "Nephronophthisis_18|not_provided": 16,
    "Nephronophthisis_18|Inborn_genetic_diseases": 14,
    "not_provided|Inborn_genetic_diseases|Nephronophthisis_18": 4,
    "Inborn_genetic_diseases|Nephronophthisis_18|not_provided": 1,
    "CEP83-related_disorder": 3,
    "CEP83-related_disorder|Nephronophthisis_18": 3,
    "not_provided|CEP83-related_disorder|Nephronophthisis_18": 1,
    "not_provided|Nephronophthisis_18": 6,
    "Nephronophthisis_18|Inborn_genetic_diseases|not_provided": 2,
    "Nephronophthisis_18|Nephronophthisis": 1,
    "Nephronophthisis_18|Inborn_genetic_diseases|not_provided|CEP83-related_disorder": 1,
    "Nephronophthisis_18|CEP83-related_disorder|not_provided": 2,
    "not_provided|Ciliopathy|Nephronophthisis_18": 1,
    "Nephronophthisis_18|not_specified": 1,
    "Nephronophthisis_18|not_provided|Inborn_genetic_diseases": 1,
    "Nephronophthisis_18|CEP83-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_23": 7,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_23": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_23|not_provided": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_23": 1,
    "NDUFA12-related_disorder": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_23|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "USP44-related_disorder": 4,
    "not_provided|USP44-related_disorder": 1,
    "USP44-related_disorder|not_provided": 1,
    "Histidinemia": 85,
    "Histidinemia|not_provided": 6,
    "not_provided|Histidinemia": 12,
    "HAL-related_disorder": 5,
    "HAL-related_disorder|Histidinemia": 2,
    "Histidinemia|not_specified": 2,
    "HAL-related_disorder|not_provided|Histidinemia": 6,
    "Increased_histidine": 3,
    "not_provided|Histidinemia|HAL-related_disorder": 1,
    "not_specified|Histidinemia": 2,
    "Spermatogenic_failure_98": 5,
    "not_provided|not_specified|Loeys-Dietz_syndrome_2": 10,
    "not_specified|Loeys-Dietz_syndrome_2": 87,
    "Loeys-Dietz_syndrome_2|not_specified": 69,
    "not_specified|Loeys-Dietz_syndrome_2|not_provided": 5,
    "Loeys-Dietz_syndrome_2|not_specified|not_provided": 8,
    "TMPO-related_disorder": 5,
    "not_specified|not_provided|Loeys-Dietz_syndrome_2": 13,
    "not_provided|Loeys-Dietz_syndrome_2|not_specified": 7,
    "not_specified|not_provided|Loeys-Dietz_syndrome_2|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1T|Loeys-Dietz_syndrome_2|not_provided": 1,
    "Loeys-Dietz_syndrome_2|not_provided|TMPO-related_disorder|not_specified": 1,
    "Loeys-Dietz_syndrome_2|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Loeys-Dietz_syndrome_2": 1,
    "not_provided|not_specified|Loeys-Dietz_syndrome_2|Cardiomyopathy": 1,
    "not_specified|Loeys-Dietz_syndrome_2|Primary_dilated_cardiomyopathy": 1,
    "High_myopia|Primary_dilated_cardiomyopathy|not_specified|not_provided|Loeys-Dietz_syndrome_2": 1,
    "Loeys-Dietz_syndrome_2|not_provided|not_specified": 7,
    "Loeys-Dietz_syndrome_2|not_specified|TMPO-related_disorder": 1,
    "Loeys-Dietz_syndrome_2|TMPO-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome_2|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|not_provided|Loeys-Dietz_syndrome_2": 1,
    "not_specified|Loeys-Dietz_syndrome_2|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Loeys-Dietz_syndrome_2|not_specified|TMPO-related_disorder|not_provided": 1,
    "Loeys-Dietz_syndrome_2|TMPO-related_disorder|not_specified": 1,
    "Loeys-Dietz_syndrome_2|TMPO-related_disorder": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Loeys-Dietz_syndrome_2|not_specified": 1,
    "not_specified|not_provided|Long_QT_syndrome|Loeys-Dietz_syndrome_2": 1,
    "not_specified|Loeys-Dietz_syndrome_2|Dilated_cardiomyopathy_1T|not_provided": 1,
    "TMPO-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|Amyloidosis|not_specified|not_provided|Dilated_cardiomyopathy_1T|Loeys-Dietz_syndrome_2|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1T": 1,
    "Loeys-Dietz_syndrome_2|Primary_dilated_cardiomyopathy|TMPO-related_disorder|not_specified|not_provided": 1,
    "not_provided|Loeys-Dietz_syndrome_2|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1T": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Loeys-Dietz_syndrome_2": 1,
    "not_specified|Loeys-Dietz_syndrome_2|not_provided|TMPO-related_disorder": 1,
    "TMPO-related_disorder|Loeys-Dietz_syndrome_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Loeys-Dietz_syndrome_2": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome|not_specified|Loeys-Dietz_syndrome_2": 1,
    "Dilated_cardiomyopathy_1T|TMPO-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy_25|Primary_dilated_cardiomyopathy|Loeys-Dietz_syndrome_2": 1,
    "TMPO-related_disorder|not_provided": 1,
    "not_provided|not_specified|TMPO-related_disorder": 1,
    "TMPO-related_disorder|not_provided|not_specified": 1,
    "not_provided|TMPO-related_disorder": 1,
    "TMPO-related_disorder|not_specified|not_provided": 1,
    "Cardiomyopathy-hypotonia-lactic_acidosis_syndrome": 23,
    "not_provided|Cardiomyopathy-hypotonia-lactic_acidosis_syndrome": 7,
    "Cardiomyopathy-hypotonia-lactic_acidosis_syndrome|not_provided": 6,
    "SLC25A3-related_disorder|not_specified|not_provided|Cardiomyopathy-hypotonia-lactic_acidosis_syndrome": 1,
    "not_provided|SLC25A3-related_disorder": 1,
    "Cardiomyopathy-hypotonia-lactic_acidosis_syndrome|not_specified|not_provided": 1,
    "not_specified|Cardiomyopathy-hypotonia-lactic_acidosis_syndrome": 2,
    "not_provided|not_specified|SLC25A3-related_disorder": 1,
    "SLC25A3-related_disorder|not_provided|not_specified": 1,
    "APAF1-related_disorder": 13,
    "APAF1-related_disorder|not_provided": 5,
    "not_provided|APAF1-related_disorder": 3,
    "ANKS1B-related_disorder": 1,
    "ANKS1B-related_neurodevelopmental_disorder": 1,
    "not_specified|not_provided|ANKS1B-related_disorder": 1,
    "Arthrogryposis_multiplex_congenita_4|_neurogenic|_with_agenesis_of_the_corpus_callosum": 9,
    "Arthrogryposis_multiplex_congenita_4|_neurogenic|_with_agenesis_of_the_corpus_callosum|not_provided": 3,
    "SCYL2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "SCYL2-related_disorder": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25": 51,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided": 7,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_25": 8,
    "SLC17A8-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_25": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided|SLC17A8-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|Inborn_genetic_diseases": 4,
    "SLC17A8-related_disorder": 5,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_25": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_25|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided": 2,
    "SLC17A8-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided": 1,
    "not_provided|SLC17A8-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_25|not_provided": 1,
    "SLC17A8-related_disorder|not_provided": 2,
    "not_provided|SLC17A8-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_25": 1,
    "not_provided|SLC17A8-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_25": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_25|Inborn_genetic_diseases": 1,
    "SLC17A8-related_disorder|not_provided|not_specified": 1,
    "SLC17A8-related_disorder|not_provided|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "not_provided|Nonsyndromic_Hearing_Loss|_Dominant": 2,
    "Cholestasis|_progressive_familial_intrahepatic|_5|not_provided": 3,
    "NR1H4-related_disorder": 15,
    "Cholestasis|_progressive_familial_intrahepatic|_5": 9,
    "NR1H4-related_disorder|not_provided": 4,
    "not_provided|NR1H4-related_disorder": 5,
    "Progressive_familial_intrahepatic_cholestasis_type_1|NR1H4-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_5": 1,
    "NR1H4-related_disorder|not_specified|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|NR1H4-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_5|not_provided": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NR1H4-related_disorder|not_provided": 1,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_5|NR1H4-related_disorder": 1,
    "not_provided|NR1H4-related_disorder|Inborn_genetic_diseases": 1,
    "Temporal_lobe_epilepsy": 1,
    "Arthrogryposis|_distal|_type_1B|not_provided": 4,
    "Arthrogryposis|_distal|_type_1B": 33,
    "not_provided|MYBPC1-related_disorder|Arthrogryposis|_distal|_type_1B": 1,
    "not_specified|not_provided|Arthrogryposis|_distal|_type_1B": 2,
    "Lethal_congenital_contracture_syndrome_4": 2,
    "not_provided|not_specified|Arthrogryposis|_distal|_type_1B": 2,
    "MYBPC1-related_disorder|Arthrogryposis|_distal|_type_1B": 2,
    "Arthrogryposis|_distal|_type_1B|not_specified|not_provided": 3,
    "not_provided|Arthrogryposis|_distal|_type_1B": 9,
    "Lethal_congenital_contracture_syndrome_4|Arthrogryposis|_distal|_type_1B|Myopathy|_congenital|_with_tremor": 3,
    "Myopathy|_congenital|_with_tremor|Lethal_congenital_contracture_syndrome_4|Arthrogryposis|_distal|_type_1B|not_provided": 1,
    "not_provided|MYBPC1-related_disorder": 2,
    "Lethal_congenital_contracture_syndrome_4|Myopathy|_congenital|_with_tremor": 1,
    "Arthrogryposis|_distal|_type_1B|Lethal_congenital_contracture_syndrome_4|Myopathy|_congenital|_with_tremor|not_provided|MYBPC1-related_disorder|not_specified": 1,
    "Myopathy|_congenital|_with_tremor": 3,
    "MYBPC1-related_disorder": 5,
    "Myopathy|_congenital|_with_tremor|Arthrogryposis|_distal|_type_1B|Lethal_congenital_contracture_syndrome_4|not_provided": 1,
    "Myopathy|_congenital|_with_tremor|not_provided": 1,
    "not_specified|Arthrogryposis|_distal|_type_1B|Myopathy|_congenital|_with_tremor|not_provided|Lethal_congenital_contracture_syndrome_4": 1,
    "not_provided|Myopathy|_congenital|_with_tremor|MYBPC1-related_disorder": 1,
    "Myopathy|_congenital|_with_tremor|not_provided|Inborn_genetic_diseases|MYBPC1-related_disorder|Arthrogryposis|_distal|_type_1B": 1,
    "Myopathy|_congenital|_with_tremor|Lethal_congenital_contracture_syndrome_4": 1,
    "Inborn_genetic_diseases|MYBPC1-related_disorder|not_provided": 1,
    "MYBPC1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Arthrogryposis|_distal|_type_1B": 2,
    "Arthrogryposis|_distal|_type_1B|Lethal_congenital_contracture_syndrome_4|Myopathy|_congenital|_with_tremor|not_provided": 1,
    "Inborn_genetic_diseases|Myopathy|_congenital|_with_tremor|Lethal_congenital_contracture_syndrome_4|Arthrogryposis|_distal|_type_1B": 1,
    "not_provided|MYBPC1-related_disorder|Inborn_genetic_diseases|Arthrogryposis|_distal|_type_1B": 1,
    "not_specified|Arthrogryposis|_distal|_type_1B|Myopathy|_congenital|_with_tremor|Lethal_congenital_contracture_syndrome_4|not_provided": 1,
    "MYBPC1-related_autosomal_recessive_non-lethal_arthrogryposis_multiplex_congenita_syndrome": 1,
    "Arthrogryposis|_distal|_type_1B|Lethal_congenital_contracture_syndrome_4|not_provided|Myopathy|_congenital|_with_tremor": 1,
    "not_specified|Arthrogryposis|_distal|_type_1B|Lethal_congenital_contracture_syndrome_4|not_provided|Myopathy|_congenital|_with_tremor": 1,
    "Arthrogryposis|_distal|_type_1B|Inborn_genetic_diseases": 2,
    "not_specified|Arthrogryposis|_distal|_type_1B|not_provided": 1,
    "MYBPC1-related_disorder|not_provided|Arthrogryposis|_distal|_type_1B": 1,
    "not_provided|Lethal_congenital_contracture_syndrome_4|Myopathy|_congenital|_with_tremor|Arthrogryposis|_distal|_type_1B": 1,
    "Lethal_congenital_contracture_syndrome_4|not_specified|Myopathy|_congenital|_with_tremor": 1,
    "Arthrogryposis|_distal|_type_1B|not_specified|Myopathy|_congenital|_with_tremor|not_provided|Lethal_congenital_contracture_syndrome_4": 1,
    "Arthrogryposis|_distal|_type_1B|not_provided|not_specified": 1,
    "Arthrogryposis|_distal|_type_1B|not_specified|not_provided|Myopathy|_congenital|_with_tremor|Lethal_congenital_contracture_syndrome_4": 1,
    "Inborn_genetic_diseases|MYBPC1-related_disorder": 1,
    "Arthrogryposis|_distal|_type_1B|MYBPC1-related_disorder": 1,
    "Arthrogryposis|_distal|_type_1B|not_provided|Lethal_congenital_contracture_syndrome_4|Myopathy|_congenital|_with_tremor": 1,
    "Lethal_congenital_contracture_syndrome_4|not_provided|Arthrogryposis|_distal|_type_1B|Myopathy|_congenital|_with_tremor|not_specified": 1,
    "Spermatogenic_failure_4|not_provided": 4,
    "not_provided|Spermatogenic_Failure": 2,
    "not_specified|Spermatogenic_failure_4": 1,
    "not_provided|Spermatogenic_failure_4": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 552,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 637,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|not_provided": 2,
    "Pseudo-Hurler_polydystrophy|not_provided|Mucolipidosis_type_II": 2,
    "Pseudo-Hurler_polydystrophy": 14,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|not_provided": 18,
    "Pseudo-Hurler_polydystrophy|not_specified|not_provided|Mucolipidosis_type_II": 1,
    "Inborn_genetic_diseases|not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 3,
    "not_specified|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 7,
    "not_specified|not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 14,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|GNPTAB-related_disorder": 8,
    "Mucolipidosis_type_II": 133,
    "Mucolipidosis": 10,
    "Mucolipidosis|not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 6,
    "GNPTAB-related_disorder|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 4,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|Mucolipidosis": 11,
    "Inborn_genetic_diseases|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 22,
    "GNPTAB-related_disorder|not_provided|Mucolipidosis|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "GNPTAB-related_disorder|Inborn_genetic_diseases|not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "Mucolipidosis|Pseudo-Hurler_polydystrophy": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|Inborn_genetic_diseases": 10,
    "Mucopolysaccharidosis|_MPS-III-A": 875,
    "GNPTAB-related_disorder": 3,
    "not_provided|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 5,
    "Mucopolysaccharidosis|_MPS-III-A|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|not_provided": 1,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|not_provided|Mucolipidosis": 1,
    "not_specified|Mucolipidosis_type_II": 1,
    "not_provided|Inborn_genetic_diseases|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 2,
    "Inborn_genetic_diseases|Mucolipidosis_type_II": 2,
    "not_provided|Mucolipidosis_type_II": 5,
    "GNPTAB-related_disorder|not_specified|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 21,
    "Inborn_genetic_diseases|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 4,
    "Mucolipidosis|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 5,
    "Mucolipidosis_type_II|Mucolipidosis|Pseudo-Hurler_polydystrophy": 2,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|Inborn_genetic_diseases|not_specified": 1,
    "GNPTAB-mucolipidosis|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "GNPTAB-related_disorder|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "not_provided|Mucolipidosis|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 4,
    "GNPTAB-related_disorder|not_provided|Mucolipidosis_type_II|Mucolipidosis|Pseudo-Hurler_polydystrophy": 1,
    "not_specified|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 4,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|GNPTAB-related_disorder|not_provided": 1,
    "not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|GNPTAB-related_disorder": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|GNPTAB-mucolipidosis": 1,
    "Inborn_genetic_diseases|Mucolipidosis_type_II|not_specified|Pseudo-Hurler_polydystrophy": 1,
    "Inborn_genetic_diseases|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|not_specified": 2,
    "GNPTAB-related_disorder|Mucolipidosis_type_II|Abnormality_of_metabolism/homeostasis|Mucolipidosis|Pseudo-Hurler_polydystrophy": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|Mucolipidosis|not_provided|Inborn_genetic_diseases": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Mucolipidosis_type_II|not_provided|Pseudo-Hurler_polydystrophy": 3,
    "Juvenile_osteochondrosis_of_spine|Legg-Calve-Perthes_disease|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "not_provided|GNPTAB-related_disorder|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 1,
    "not_provided|Mucolipidosis_type_II|Mucolipidosis": 1,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|not_specified": 1,
    "GNPTAB-related_disorder|not_provided|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 1,
    "Mucolipidosis_type_II|GNPTAB-related_disorder|Pseudo-Hurler_polydystrophy": 1,
    "not_specified|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|not_provided": 1,
    "Mucolipidosis_type_II|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-III-A|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy": 3,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis|Mucolipidosis_type_II|Mucolipidosis_III_alpha/beta|_atypical": 1,
    "not_provided|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|Mucolipidosis": 1,
    "Mucolipidosis|GNPTAB-related_disorder|Mucolipidosis_type_II|Pseudo-Hurler_polydystrophy|not_provided": 1,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|Inborn_genetic_diseases": 1,
    "Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|Inborn_genetic_diseases|not_provided": 1,
    "Mucolipidosis|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 2,
    "not_specified|Pseudo-Hurler_polydystrophy": 1,
    "not_specified|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II|not_provided": 1,
    "GNPTAB-mucolipidosis": 1,
    "not_specified|not_provided|Pseudo-Hurler_polydystrophy|Mucolipidosis_type_II": 1,
    "Microcephaly_24|_primary|_autosomal_recessive": 5,
    "NUP37-related_disorder": 4,
    "NUP37-related_disorder|Microcephaly_24|_primary|_autosomal_recessive": 1,
    "not_provided|NUP37-related_disorder": 1,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency": 13,
    "Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency": 113,
    "Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency|not_provided": 15,
    "IGF1-related_disorder": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency|not_specified|not_provided": 1,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency|Inborn_genetic_diseases|IGF1-related_disorder|not_specified": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency|IGF1-related_disorder|not_provided": 1,
    "not_specified|IGF1-related_disorder|not_provided": 1,
    "not_provided|IGF1-related_disorder|Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Growth_delay_due_to_insulin-like_growth_factor_type_1_deficiency": 1,
    "not_provided|Phenylketonuria": 246,
    "PAH-related_disorder|Phenylketonuria": 5,
    "Phenylketonuria|not_specified": 7,
    "Phenylketonuria|Inborn_genetic_diseases": 7,
    "PAH-related_disorder|not_provided|Phenylketonuria": 15,
    "not_specified|Phenylketonuria": 11,
    "not_specified|not_provided|Phenylketonuria": 8,
    "not_provided|not_specified|Phenylketonuria": 5,
    "Phenylketonuria|not_provided": 169,
    "PAH-related_disorder|Inborn_genetic_diseases|not_provided|Pituitary_hormone_deficiency|_combined|_2|Phenylketonuria": 1,
    "Inborn_genetic_diseases|Phenylketonuria": 7,
    "PAH-related_disorder|not_provided|Hyperphenylalaninemia|Phenylketonuria": 1,
    "PAH-related_disorder|not_provided|Phenylketonuria|Hyperphenylalaninemia|See_cases": 1,
    "not_provided|PAH-related_disorder|Phenylketonuria": 1,
    "PAH-related_disorder|not_provided|Phenylketonuria|Hyperphenylalaninemia": 2,
    "PAH-related_disorder|Inborn_genetic_diseases|not_provided|Phenylketonuria|See_cases": 2,
    "PAH-related_disorder|Inborn_genetic_diseases|not_provided|Phenylketonuria": 7,
    "See_cases|Phenylketonuria": 1,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Phenylketonuria": 1,
    "Phenylketonuria|not_provided|PAH-related_disorder": 4,
    "Mild_hyperphenylalaninemia|PAH-related_disorder|not_provided|Phenylketonuria|Hyperphenylalaninemia": 1,
    "Malignant_tumor_of_breast|Phenylketonuria|not_provided": 1,
    "PAH-related_disorder|not_provided|Phenylketonuria|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis": 1,
    "not_specified|Phenylketonuria|not_provided": 6,
    "not_provided|Phenylketonuria|not_specified": 4,
    "Marfanoid_habitus_and_intellectual_disability|PAH-related_disorder|Inborn_genetic_diseases|not_provided|Phenylketonuria|Hyperphenylalaninemia|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Hyperphenylalaninemia|Phenylketonuria": 3,
    "Phenylketonuria|Hyperphenylalaninemia|not_provided": 3,
    "not_provided|Phenylketonuria|Intellectual_disability": 1,
    "Inborn_genetic_diseases|PAH-related_disorder|not_provided|Phenylketonuria|See_cases": 1,
    "Hyperphenylalaninemia|not_provided|Phenylketonuria": 1,
    "Mild_non-PKU_hyperphenylalanemia|See_cases|Phenylketonuria|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Phenylketonuria": 1,
    "Phenylketonuria|not_provided|See_cases": 1,
    "not_provided|Hyperphenylalaninemia|Phenylketonuria": 5,
    "PAH-related_disorder|Inborn_genetic_diseases|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_provided|Phenylketonuria": 1,
    "Inborn_genetic_diseases|not_provided|Phenylketonuria|PAH-related_disorder|not_specified": 1,
    "PAH-related_disorder|Phenylketonuria|not_provided": 1,
    "Phenylketonuria|See_cases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Phenylketonuria": 7,
    "not_provided|Pulmonary_hypertension|_primary|_1|Phenylketonuria": 1,
    "PAH-related_disorder|Phenylketonuria|Inborn_genetic_diseases|not_provided": 1,
    "Phenylketonuria|not_provided|Pulmonary_hypertension|_primary|_1|See_cases": 1,
    "PAH-related_disorder|Inborn_genetic_diseases|not_provided|Hyperphenylalaninemia|Phenylketonuria": 1,
    "Phenylketonuria|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Phenylketonuria|PAH-related_disorder": 2,
    "PAH-related_disorder|Phenylketonuria|not_specified": 1,
    "not_provided|Phenylketonuria|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Phenylketonuria": 2,
    "Hyperphenylalaninemia|Phenylketonuria|not_provided": 1,
    "PAH-related_disorder|Inborn_genetic_diseases|not_provided|Phenylketonuria|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "Phenylketonuria|Inborn_genetic_diseases|not_provided|Hyperphenylalaninemia|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|See_cases": 1,
    "not_provided|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Phenylketonuria": 1,
    "Inborn_genetic_diseases|PAH-related_disorder|not_provided|Phenylketonuria": 1,
    "Phenylketonuria|RASopathy": 1,
    "Inborn_genetic_diseases|not_provided|Pulmonary_hypertension|_primary|_1|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Phenylketonuria": 1,
    "not_provided|See_cases|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Phenylketonuria": 1,
    "Phenylketonuria|not_specified|not_provided": 3,
    "Phenylketonuria|PAH-related_disorder|See_cases|not_provided": 1,
    "Phenylketonuria|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Phenylketonuria|not_provided": 1,
    "PAH-related_disorder|Mild_non-PKU_hyperphenylalanemia|not_specified|not_provided|Phenylketonuria": 1,
    "not_specified|PAH-related_disorder|Phenylketonuria": 1,
    "Inborn_genetic_diseases|Phenylketonuria|PAH-related_disorder|not_provided|Hyperphenylalaninemia": 1,
    "6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency|Phenylketonuria|Propionic_acidemia": 1,
    "Phenylketonuria|PAH-related_disorder|not_provided": 1,
    "PAH-related_disorder|not_provided|Hyperphenylalaninemia|Phenylketonuria|See_cases": 1,
    "PAH-related_disorder|not_specified|not_provided|Phenylketonuria": 2,
    "Phenylketonuria|not_provided|Hyperphenylalaninemia": 1,
    "not_provided|PAH-related_disorder|Phenylketonuria|not_specified": 1,
    "Phenylketonuria|Inborn_genetic_diseases|not_provided": 1,
    "Hyperphenylalaninemia|Phenylketonuria": 1,
    "ASCL1-related_disorder": 3,
    "ASCL1-related_disorder|not_specified|not_provided": 3,
    "Central_hypoventilation_syndrome|_congenital|_1|_with_or_without_Hirschsprung_disease|not_specified|not_provided": 1,
    "ASCL1-related_disorder|not_specified": 2,
    "ASCL1-related_disorder|Phenylketonuria": 1,
    "CHST11-related_disorder": 4,
    "Osteochondrodysplasia|_brachydactyly|_and_overlapping_malformed_digits|Chondrodysplasia|clino-symphalangism|overriding_digits|Brachydactyly|Synpolydactyly_type_1": 1,
    "not_specified|Osteochondrodysplasia|_brachydactyly|_and_overlapping_malformed_digits": 1,
    "not_provided|CHST11-related_disorder": 1,
    "not_provided|WASHC4-related_disorder": 2,
    "not_provided|WASHC4-related_disorder|Intellectual_disability|_autosomal_recessive_43": 1,
    "WASHC4-related_disorder": 4,
    "WASHC4-related_disorder|not_provided": 3,
    "Intellectual_disability|_autosomal_recessive_43|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_43": 14,
    "not_specified|Intellectual_disability|_autosomal_recessive_43": 2,
    "not_specified|WASHC4-related_disorder|not_provided": 1,
    "WASHC4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_recessive_43": 1,
    "not_provided|not_specified|WASHC4-related_disorder": 1,
    "not_provided|WASHC4-related_disorder|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_43|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_43|not_provided|Intellectual_disability": 1,
    "NUAK1-related_disorder": 2,
    "POLR-related_leukodystrophy|not_provided": 2,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 85,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided": 19,
    "not_provided|POLR3B-related_disorder": 3,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|not_provided": 3,
    "POLR3B-related_disorder": 8,
    "not_provided|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 28,
    "not_provided|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 2,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 2,
    "not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 2,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 7,
    "POLR3B-related_disorder|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|not_provided": 2,
    "POLR3B-related_disorder|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|POLR3B-related_disorder|not_provided": 1,
    "not_provided|not_specified|POLR3B-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|POLR3B-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|See_cases|POLR-related_leukodystrophy|Intellectual_disability|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Amenorrhea": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|See_cases": 1,
    "not_provided|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|POLR3B-related_disorder|Hypogonadotropic_hypogonadism|POLR-related_leukodystrophy|not_specified|not_provided|See_cases": 1,
    "POLR3B-related_disorder|not_provided": 2,
    "not_provided|not_specified|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|not_provided": 2,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|not_provided|Leukoencephalopathy|_ataxia|_hypodontia|_hypomyelination_syndrome": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_specified|not_provided": 2,
    "not_provided|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|POLR-related_leukodystrophy": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I|POLR3B-related_disorder|POLR-related_leukodystrophy|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided": 1,
    "not_provided|POLR-related_leukodystrophy|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 1,
    "not_provided|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Leukodystrophy": 1,
    "See_cases|POLR3B-related_disorder|not_provided": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Inborn_genetic_diseases|not_provided": 2,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1I": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|Amenorrhea": 1,
    "Inborn_genetic_diseases|not_provided|POLR3B-related_disorder": 1,
    "POLR3B-related_disorder|See_cases|not_provided": 1,
    "Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|VISS_syndrome": 1,
    "not_specified|Hypomyelinating_leukodystrophy_8_with_or_without_oligodontia_and-or_hypogonadotropic_hypogonadism|not_provided": 1,
    "RFX4-related_disorder": 1,
    "not_specified|RFX4-related_disorder": 1,
    "Delayed_sleep_phase_syndrome|_susceptibility_to|Sleep-wake_schedule_disorder|_delayed_phase_type|Attention_deficit_hyperactivity_disorder": 1,
    "CRY1-related_disorder": 7,
    "CRY1-related_disorder|not_provided": 1,
    "not_provided|CRY1-related_disorder": 1,
    "Sleep-wake_schedule_disorder|_delayed_phase_type|Attention_deficit_hyperactivity_disorder": 1,
    "Delayed_sleep_phase_syndrome|_susceptibility_to": 2,
    "Intellectual_disability|_Neurodevelopmental_defects_and_Developmental_delay_with_46|XY_gonadal_dysgenesis": 8,
    "Porokeratosis_3|_disseminated_superficial_actinic_type": 6,
    "ISCU-related_disorder|not_provided|Hereditary_myopathy_with_lactic_acidosis_due_to_ISCU_deficiency": 1,
    "not_provided|Hereditary_myopathy_with_lactic_acidosis_due_to_ISCU_deficiency": 4,
    "Hereditary_myopathy_with_lactic_acidosis_due_to_ISCU_deficiency|not_provided": 4,
    "ISCU-related_disorder|not_provided": 1,
    "not_provided|ISCU-related_disorder|not_specified": 1,
    "not_provided|not_specified|Hereditary_myopathy_with_lactic_acidosis_due_to_ISCU_deficiency": 1,
    "Hereditary_myopathy_with_lactic_acidosis_due_to_ISCU_deficiency": 4,
    "ISCU-related_disorder": 4,
    "not_provided|ISCU-related_disorder": 2,
    "Myopathy|not_provided": 1,
    "SELPLG-related_disorder": 5,
    "SELPLG-related_disorder|not_provided": 1,
    "SSH1-related_disorder": 4,
    "DAO-related_disorder": 27,
    "not_provided|DAO-related_disorder": 3,
    "DAO-related_disorder|not_provided": 5,
    "DAO-related_disorder|Amyotrophic_lateral_sclerosis": 1,
    "Amyotrophic_lateral_sclerosis|DAO-related_disorder": 1,
    "Hyper-IgM_syndrome_type_5": 234,
    "Hyper-IgM_syndrome_type_5|not_specified": 7,
    "UNG-related_disorder": 1,
    "not_specified|Hyper-IgM_syndrome_type_5": 10,
    "UNG-related_disorder|not_provided|Hyper-IgM_syndrome_type_5": 1,
    "not_provided|Hyper-IgM_syndrome_type_5": 3,
    "Hyper-IgM_syndrome_type_5|not_provided": 4,
    "Hyper-IgM_syndrome_type_5|not_specified|not_provided": 1,
    "Hyper-IgM_syndrome_type_5|UNG-related_disorder|not_provided": 1,
    "UNG-related_disorder|Hyper-IgM_syndrome_type_5": 2,
    "not_specified|Hyper-IgM_syndrome_type_5|not_provided": 1,
    "not_provided|ACACB-related_disorder": 18,
    "not_specified|ACACB-related_disorder": 1,
    "ACACB-related_disorder": 45,
    "ACACB-related_disorder|not_provided": 13,
    "ACACB-related_disorder|not_specified": 1,
    "not_specified|ACACB-related_disorder|not_provided": 2,
    "Central_hypoventilation_syndrome|_congenital|_2|_and_autonomic_dysfunction": 9,
    "Central_hypoventilation_syndrome|_congenital|_2|_and_autonomic_dysfunction|not_specified": 1,
    "Inborn_genetic_diseases|Oculocerebrofacial_syndrome|_Kaufman_type|not_provided": 3,
    "Oculocerebrofacial_syndrome|_Kaufman_type": 35,
    "UBE3B-related_disorder|not_provided": 7,
    "Oculocerebrofacial_syndrome|_Kaufman_type|not_provided": 3,
    "UBE3B-related_disorder": 2,
    "not_provided|Oculocerebrofacial_syndrome|_Kaufman_type": 4,
    "Inborn_genetic_diseases|Oculocerebrofacial_syndrome|_Kaufman_type": 1,
    "Oculocerebrofacial_syndrome|_Kaufman_type|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Oculocerebrofacial_syndrome|_Kaufman_type": 1,
    "Oculocerebrofacial_syndrome|_Kaufman_type|Inborn_genetic_diseases|not_provided": 1,
    "Optic_nerve_hypoplasia|Oculocerebrofacial_syndrome|_Kaufman_type": 1,
    "Methylmalonic_aciduria|_cblB_type|not_provided": 29,
    "not_provided|Methylmalonic_aciduria|_cblB_type": 13,
    "MMAB-related_disorder|not_specified|Methylmalonic_aciduria|_cblB_type": 1,
    "Methylmalonic_aciduria|_cblB_type|Inborn_genetic_diseases": 8,
    "not_specified|not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|Methylmalonic_aciduria|_cblB_type": 1,
    "not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblB_type": 2,
    "Inborn_genetic_diseases|Methylmalonic_aciduria|_cblB_type": 7,
    "MMAB-related_disorder|Methylmalonic_aciduria|_cblB_type": 4,
    "not_specified|Methylmalonic_aciduria|_cblB_type": 4,
    "Inborn_genetic_diseases|not_provided|Methylmalonic_aciduria|_cblB_type": 5,
    "not_specified|not_provided|Methylmalonic_aciduria|_cblB_type": 3,
    "Methylmalonic_aciduria|_cblB_type|not_specified": 5,
    "Methylmalonic_aciduria|_cblB_type|not_provided|Inborn_genetic_diseases": 2,
    "Methylmalonic_aciduria|_cblB_type|Methylmalonic_acidemia": 4,
    "not_provided|Methylmalonic_aciduria|_cblB_type|Methylmalonic_acidemia": 1,
    "MMAB-related_disorder|Inborn_genetic_diseases|not_provided|Methylmalonic_acidemia|Methylmalonic_aciduria|_cblB_type": 1,
    "Methylmalonic_aciduria|_cblB_type|not_provided|MMAB-related_disorder": 2,
    "Methylmalonic_acidemia|Methylmalonic_aciduria|_cblB_type": 2,
    "Methylmalonic_aciduria|_cblB_type|not_specified|not_provided": 1,
    "MMAB-related_disorder|not_specified|not_provided|Methylmalonic_aciduria|_cblB_type": 1,
    "not_provided|Methylmalonic_aciduria|_cblB_type|Inborn_genetic_diseases": 1,
    "Methylmalonic_aciduria|_cblB_type|MMAB-related_disorder": 2,
    "not_provided|Methylmalonic_aciduria|_cblB_type|not_specified": 1,
    "Methylmalonic_aciduria|_cblB_type|not_provided|Methylmalonic_acidemia": 2,
    "Methylmalonic_aciduria|_cblB_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|not_provided|not_specified|Methylmalonic_acidemia": 1,
    "Methylmalonic_aciduria|_cblB_type|Methylmalonic_aciduria|Methylmalonic_acidemia": 1,
    "MMAB-related_disorder|not_specified|not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Methylmalonic_aciduria|_cblB_type": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Methylmalonic_aciduria|_cblB_type|not_specified|not_provided|Methylmalonic_acidemia": 1,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Methylmalonic_aciduria|_cblB_type|not_provided|not_specified|Methylmalonic_acidemia": 1,
    "not_specified|MMAB-related_disorder": 1,
    "Methylmalonic_acidemia|not_specified|Methylmalonic_aciduria|_cblB_type": 1,
    "Methylmalonic_aciduria|_cblB_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever": 42,
    "not_specified|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 2,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Autoinflammatory_syndrome|not_provided|Methylmalonic_acidemia": 1,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 12,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 9,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type": 34,
    "not_provided|not_specified|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 1,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_specified": 7,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_provided": 8,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 264,
    "not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Autoinflammatory_syndrome|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 11,
    "Mevalonic_aciduria": 5,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 42,
    "Mevalonic_aciduria|Retinal_dystrophy|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria": 12,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 27,
    "Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|not_provided": 1,
    "not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 6,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 28,
    "MVK-related_disorder|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified|not_provided": 1,
    "not_provided|Hyperimmunoglobulin_D_with_periodic_fever": 3,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Inborn_genetic_diseases": 1,
    "Deficiency_of_mevalonate_kinase": 2,
    "Autoinflammatory_syndrome|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 5,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_provided|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 4,
    "not_specified|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|not_provided|Autoinflammatory_syndrome|Methylmalonic_acidemia": 1,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Inborn_genetic_diseases|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type": 2,
    "not_provided|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 1,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Autoinflammatory_syndrome|MVK-related_disorder|not_provided": 1,
    "Autoinflammatory_syndrome|MVK-related_disorder|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_specified|not_provided": 1,
    "not_provided|not_specified|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Autoinflammatory_syndrome|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_provided": 4,
    "MVK-related_disorder|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Inborn_genetic_diseases|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 1,
    "MVK-related_disorder|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|not_provided|See_cases": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 1,
    "not_provided|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 2,
    "not_provided|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Autoinflammatory_syndrome": 1,
    "not_provided|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified": 1,
    "Retinal_dystrophy|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|not_provided": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified|Autoinflammatory_syndrome|not_provided": 1,
    "Deficiency_of_mevalonate_kinase|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_provided": 1,
    "not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Autoinflammatory_syndrome|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_provided|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 4,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified|not_provided|Retinal_dystrophy|Autoinflammatory_syndrome": 1,
    "not_provided|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Inborn_genetic_diseases": 1,
    "MVK-related_disorder|not_provided|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "not_specified|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 2,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Inborn_genetic_diseases": 1,
    "not_provided|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 3,
    "MVK-related_disorder|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "MVK-related_disorder|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 2,
    "MVK-related_disorder|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 2,
    "Autoinflammatory_syndrome|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 1,
    "not_provided|Autoinflammatory_syndrome|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|not_provided|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria": 1,
    "Deficiency_of_mevalonate_kinase|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 2,
    "not_specified|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|not_provided": 1,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|not_specified": 1,
    "not_specified|not_provided|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Inborn_genetic_diseases|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "not_provided|Hyperimmunoglobulin_D_with_periodic_fever|MVK-related_disorder|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Inborn_genetic_diseases|not_provided": 1,
    "Autoinflammatory_syndrome|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|not_specified": 1,
    "Autoinflammatory_syndrome|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_specified|Autoinflammatory_syndrome|not_provided": 1,
    "MVK-related_disorder": 2,
    "Autoinflammatory_syndrome|not_specified|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|not_provided|Nemaline_myopathy_5": 1,
    "not_provided|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Autoinflammatory_syndrome|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Inborn_genetic_diseases|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Inborn_genetic_diseases|not_provided|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Nemaline_myopathy_6": 1,
    "Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|not_specified|not_provided": 1,
    "Retinal_dystrophy|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Autoinflammatory_syndrome|MVK-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Porokeratosis_3|_disseminated_superficial_actinic_type|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Retinal_dystrophy|not_specified": 1,
    "Inborn_genetic_diseases|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|not_provided": 1,
    "not_provided|MVK-related_disorder|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "not_specified|not_provided|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 2,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Inborn_genetic_diseases|not_provided": 1,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|not_provided|Porokeratosis_3|_disseminated_superficial_actinic_type|Autoinflammatory_syndrome|not_specified": 1,
    "not_specified|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|not_provided|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Retinal_dystrophy|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|not_provided": 1,
    "not_specified|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria": 1,
    "not_specified|Autoinflammatory_syndrome|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Autoinflammatory_syndrome|not_provided": 1,
    "Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type|Retinal_dystrophy|not_provided": 1,
    "not_specified|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Deficiency_of_mevalonate_kinase|not_provided": 1,
    "Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Autoinflammatory_syndrome": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Inborn_genetic_diseases|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|not_specified": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_provided": 1,
    "not_provided|Retinal_dystrophy|Porokeratosis_3|_disseminated_superficial_actinic_type|Mevalonic_aciduria|Hyperimmunoglobulin_D_with_periodic_fever": 1,
    "Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Autoinflammatory_syndrome|Inborn_genetic_diseases|MVK-related_disorder|Porokeratosis_3|_disseminated_superficial_actinic_type|Retinal_dystrophy|not_specified|not_provided": 1,
    "Deficiency_of_mevalonate_kinase|MVK-related_disorder|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|not_provided": 1,
    "MVK-related_disorder|Porokeratosis_3|_disseminated_superficial_actinic_type|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|not_provided": 1,
    "MVK-related_disorder|Hyperimmunoglobulin_D_with_periodic_fever|Mevalonic_aciduria|Porokeratosis_3|_disseminated_superficial_actinic_type": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "not_provided|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 2,
    "Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 2,
    "Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 2,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type": 4,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 2,
    "Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C": 2,
    "TRPV4-related_disorder|not_provided": 2,
    "Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C": 10,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases": 22,
    "Charcot-Marie-Tooth_disease_axonal_type_2C": 555,
    "Inborn_genetic_diseases|Connective_tissue_disorder|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C": 3,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 51,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases": 5,
    "not_provided|Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_provided": 2,
    "Mild_short_stature": 1,
    "not_provided|TRPV4-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2C|Connective_tissue_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided": 39,
    "Connective_tissue_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_specified": 2,
    "Distal_myopathy|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C": 21,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease": 3,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C": 11,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Spondylometaphyseal_dysplasia|Brachyolmia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Charcot-Marie-Tooth_disease_type_2|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|TRPV4-related_disorder": 4,
    "Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Parastremmatic_dwarfism|Avascular_necrosis_of_femoral_head|_primary|_2|Metatropic_dysplasia|Familial_digital_arthropathy-brachydactyly|Brachyrachia_(short_spine_dysplasia)|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Connective_tissue_disorder|not_specified|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified": 10,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided": 5,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C": 4,
    "not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease|Connective_tissue_disorder|Inborn_genetic_diseases|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "not_specified|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Avascular_necrosis_of_femoral_head|_primary|_2|Metatropic_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Scapuloperoneal_spinal_muscular_atrophy|Familial_digital_arthropathy-brachydactyly|Parastremmatic_dwarfism|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Neuromuscular_disease|Skeletal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type": 1,
    "TRPV4-related_disorder": 6,
    "Inborn_genetic_diseases|not_provided|Skeletal_dysplasia|Parastremmatic_dwarfism|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia": 1,
    "Neuromuscular_disease|Skeletal_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "Skeletal_dysplasia|Metatropic_dysplasia": 2,
    "Metatropic_dysplasia": 7,
    "Neuromuscular_disease|Skeletal_dysplasia|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 11,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Familial_digital_arthropathy-brachydactyly|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Avascular_necrosis_of_femoral_head|_primary|_2|Brachyrachia_(short_spine_dysplasia)|Parastremmatic_dwarfism|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Sodium_serum_level_quantitative_trait_locus_1": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Connective_tissue_disorder|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified|Inborn_genetic_diseases": 4,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided|Inborn_genetic_diseases": 6,
    "not_specified|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Inborn_genetic_diseases|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_provided": 7,
    "Inborn_genetic_diseases|TRPV4-related_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Charcot-Marie-Tooth_disease_axonal_type_2C|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases": 1,
    "Neuromuscular_disease|Skeletal_dysplasia|Metatropic_dysplasia": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_specified": 4,
    "Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Skeletal_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Connective_tissue_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified|not_provided|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease|not_specified|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|TRPV4-related_bone_disorder|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Familial_digital_arthropathy-brachydactyly|Sodium_serum_level_quantitative_trait_locus_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Avascular_necrosis_of_femoral_head|_primary|_2|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia|Parastremmatic_dwarfism|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia|Scapuloperoneal_spinal_muscular_atrophy|Sodium_serum_level_quantitative_trait_locus_1|Parastremmatic_dwarfism|Spondylometaphyseal_dysplasia|_Kozlowski_type|Avascular_necrosis_of_femoral_head|_primary|_2|Familial_digital_arthropathy-brachydactyly|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|Connective_tissue_disorder|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 2,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C": 6,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Charcot-Marie-Tooth_disease|Neuromuscular_disease|Skeletal_dysplasia|not_provided|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Skeletal_dysplasia|not_provided|Metatropic_dysplasia": 1,
    "not_provided|Skeletal_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "not_provided|Skeletal_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|not_specified|not_provided|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Avascular_necrosis_of_femoral_head|_primary|_2": 1,
    "Skeletal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 2,
    "Multiple_epiphyseal_dysplasia|Neuromuscular_disease|Skeletal_dysplasia|Inborn_genetic_diseases|not_provided|Parastremmatic_dwarfism|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Neuromuscular_disease|Skeletal_dysplasia": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Connective_tissue_disorder|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|not_specified|Brachyrachia_(short_spine_dysplasia)|Inborn_genetic_diseases|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "TRPV4-related_disorder|Charcot-Marie-Tooth_disease|Connective_tissue_disorder|not_specified|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C": 2,
    "Connective_tissue_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)": 1,
    "Avascular_necrosis_of_femoral_head|_primary|_2|Familial_digital_arthropathy-brachydactyly|Parastremmatic_dwarfism|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Sodium_serum_level_quantitative_trait_locus_1|Metatropic_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C": 2,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|TRPV4-related_bone_disorder|Scapuloperoneal_spinal_muscular_atrophy|Inborn_genetic_diseases": 1,
    "Neuromuscular_disease|Skeletal_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease": 1,
    "Spondylometaphyseal_dysplasia|_Kozlowski_type|not_provided|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia": 1,
    "TRPV4-related_disorder|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Connective_tissue_disorder|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "TRPV4-related_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Familial_digital_arthropathy-brachydactyly|Parastremmatic_dwarfism|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Avascular_necrosis_of_femoral_head|_primary|_2|Brachyrachia_(short_spine_dysplasia)|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Sodium_serum_level_quantitative_trait_locus_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Inborn_genetic_diseases|not_provided|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Skeletal_dysplasia_and_progressive_central_nervous_system_degeneration|_lethal|Skeletal_dysplasia|not_provided|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "not_specified|not_provided|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|TRPV4-related_disorder|Inborn_genetic_diseases|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Scapuloperoneal_spinal_muscular_atrophy|TRPV4-related_bone_disorder": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Tip-toe_gait|not_provided": 1,
    "TRPV4-related_disorder|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Inborn_genetic_diseases|not_provided|Metatropic_dysplasia|Parastremmatic_dwarfism|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Familial_digital_arthropathy-brachydactyly|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Avascular_necrosis_of_femoral_head|_primary|_2|Sodium_serum_level_quantitative_trait_locus_1|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)": 1,
    "Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Scapuloperoneal_spinal_muscular_atrophy": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided|TRPV4-related_disorder": 1,
    "Connective_tissue_disorder|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "TRPV4-associated_skeletal_dysplasias|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Skeletal_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 2,
    "Parastremmatic_dwarfism": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 2,
    "Parastremmatic_dwarfism|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Familial_digital_arthropathy-brachydactyly|Metatropic_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C|Avascular_necrosis_of_femoral_head|_primary|_2|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Inborn_genetic_diseases|not_provided|Scapuloperoneal_spinal_muscular_atrophy|TRPV4-related_disorder": 1,
    "Inborn_genetic_diseases|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "TRPV4-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|not_specified|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Skeletal_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_type_4|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "TRPV4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Charcot-Marie-Tooth_disease|Neuromuscular_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Lower_limb_amyotrophy|EMG_abnormality|Clubfoot": 1,
    "TRPV4-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Neuromuscular_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "TRPV4-related_disorder|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|TRPV4-Associated_Disorders|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Neuromuscular_disease|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Brachyrachia_(short_spine_dysplasia)|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "See_cases|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease": 3,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|TRPV4-related_disorder|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Familial_digital_arthropathy-brachydactyly|Parastremmatic_dwarfism|Charcot-Marie-Tooth_disease_axonal_type_2C|Sodium_serum_level_quantitative_trait_locus_1|Avascular_necrosis_of_femoral_head|_primary|_2|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Charcot-Marie-Tooth_disease|not_specified|Connective_tissue_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided": 1,
    "Neuromuscular_disease|Skeletal_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Neuromuscular_disease|Skeletal_dysplasia|not_provided|Metatropic_dysplasia": 1,
    "Familial_digital_arthropathy-brachydactyly|not_provided": 1,
    "Familial_digital_arthropathy-brachydactyly": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Inborn_genetic_diseases|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "TRPV4-related_bone_disorder|Scapuloperoneal_spinal_muscular_atrophy|Parastremmatic_dwarfism|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Avascular_necrosis_of_femoral_head|_primary|_2|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Familial_digital_arthropathy-brachydactyly|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Charcot-Marie-Tooth_disease|Neuromuscular_disease|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_motor_neuron_disease|Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|Neuromuscular_disease|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|TRPV4-related_disorder|Inborn_genetic_diseases|not_specified|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Tip-toe_gait": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Neuromuscular_disease|Skeletal_dysplasia|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Scapuloperoneal_spinal_muscular_atrophy|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Brachyrachia_(short_spine_dysplasia)|Parastremmatic_dwarfism|Familial_digital_arthropathy-brachydactyly|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Avascular_necrosis_of_femoral_head|_primary|_2": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2C|TRPV4-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "TRPV4-related_disorder|Connective_tissue_disorder|not_specified|Neuromuscular_disease|Skeletal_dysplasia|Charcot-Marie-Tooth_disease|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "not_provided|Familial_digital_arthropathy-brachydactyly|Sodium_serum_level_quantitative_trait_locus_1|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Avascular_necrosis_of_femoral_head|_primary|_2|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia|Parastremmatic_dwarfism|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "Neuromuscular_disease|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|TRPV4-related_disorder|not_specified": 1,
    "Skeletal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8": 1,
    "TRPV4-related_disorder|Inborn_genetic_diseases|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified": 1,
    "Connective_tissue_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant": 1,
    "TRPV4-related_disorder|Skeletal_dysplasia|Metatropic_dysplasia": 1,
    "TRPV4-related_bone_disorder": 1,
    "Congenital_myopathy|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "not_specified|not_provided|See_cases|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Connective_tissue_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Metatropic_dysplasia|Parastremmatic_dwarfism|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Scapuloperoneal_spinal_muscular_atrophy|Avascular_necrosis_of_femoral_head|_primary|_2|Brachyrachia_(short_spine_dysplasia)|Familial_digital_arthropathy-brachydactyly|Spondylometaphyseal_dysplasia|_Kozlowski_type|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided|Brachyrachia_(short_spine_dysplasia)|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Avascular_necrosis_of_femoral_head|_primary|_2|Parastremmatic_dwarfism|Sodium_serum_level_quantitative_trait_locus_1|Familial_digital_arthropathy-brachydactyly|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Scapuloperoneal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease|Familial_digital_arthropathy-brachydactyly|Metatropic_dysplasia|Spondyloepimetaphyseal_dysplasia|_Maroteaux_type|Scapuloperoneal_spinal_muscular_atrophy|Avascular_necrosis_of_femoral_head|_primary|_2|Parastremmatic_dwarfism|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Distal_spinal_muscular_atrophy|Inborn_genetic_diseases": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Charcot-Marie-Tooth_disease_axonal_type_2C|Spondylometaphyseal_dysplasia|_Kozlowski_type": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2C|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Tip-toe_gait|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Connective_tissue_disorder|Charcot-Marie-Tooth_disease|not_provided|not_specified|Scapuloperoneal_spinal_muscular_atrophy|Sodium_serum_level_quantitative_trait_locus_1|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|not_specified|Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Brachyrachia_(short_spine_dysplasia)|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2C|Distal_spinal_muscular_atrophy|not_provided": 1,
    "Inborn_genetic_diseases|Connective_tissue_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided|Scapuloperoneal_spinal_muscular_atrophy|Spondylometaphyseal_dysplasia|_Kozlowski_type|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Metatropic_dysplasia|Brachyrachia_(short_spine_dysplasia)": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_axonal_type_2C": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2C|not_specified": 1,
    "Scapuloperoneal_spinal_muscular_atrophy|Charcot-Marie-Tooth_disease_axonal_type_2C|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Metatropic_dysplasia|Spondylometaphyseal_dysplasia|_Kozlowski_type|Brachyrachia_(short_spine_dysplasia)": 1,
    "Spondylometaphyseal_dysplasia|_Kozlowski_type|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Charcot-Marie-Tooth_disease_axonal_type_2C|Scapuloperoneal_spinal_muscular_atrophy|Brachyrachia_(short_spine_dysplasia)": 1,
    "not_provided|Spondylometaphyseal_dysplasia|Scapuloperoneal_spinal_muscular_atrophy|Metatropic_dysplasia|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_8|Brachyolmia|Charcot-Marie-Tooth_disease_type_2": 1,
    "IFT81-related_disorder|not_provided": 4,
    "SHORT-RIB_THORACIC_DYSPLASIA_19_WITHOUT_POLYDACTYLY|Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly": 3,
    "Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly": 5,
    "not_provided|IFT81-related_disorder": 1,
    "Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly|not_provided": 1,
    "Short_rib-polydactyly_syndrome|Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly": 1,
    "SHORT-RIB_THORACIC_DYSPLASIA_19_WITHOUT_POLYDACTYLY|Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly|not_provided|Jeune_thoracic_dystrophy|Retinal_dystrophy": 1,
    "not_provided|Short-rib_thoracic_dysplasia_19_with_or_without_polydactyly|Ciliopathy": 1,
    "Keratosis_follicularis": 85,
    "Keratosis_follicularis|not_provided": 9,
    "not_specified|not_provided|Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis": 3,
    "Keratosis_follicularis|Acrokeratosis_verruciformis_of_Hopf|not_specified|not_provided": 1,
    "not_provided|Acrokeratosis_verruciformis_of_Hopf": 2,
    "not_provided|Keratosis_follicularis": 7,
    "not_provided|Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis|not_specified": 1,
    "Keratosis_follicularis|not_specified|Inborn_genetic_diseases": 1,
    "Keratosis_follicularis|Inborn_genetic_diseases": 3,
    "not_specified|Keratosis_follicularis|Acrokeratosis_verruciformis_of_Hopf|not_provided": 1,
    "Acrokeratosis_verruciformis_of_Hopf": 3,
    "Darier_disease|_acral_hemorrhagic_type": 1,
    "ATP2A2-related_disorder": 6,
    "Keratosis_follicularis|Acrokeratosis_verruciformis_of_Hopf|not_provided|not_specified": 1,
    "not_provided|ATP2A2-related_disorder|Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis": 1,
    "Keratosis_follicularis|Acrokeratosis_verruciformis_of_Hopf|not_provided|ATP2A2-related_disorder": 1,
    "not_provided|Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis": 4,
    "ATP2A2-related_disorder|not_provided|Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis": 1,
    "Inborn_genetic_diseases|Keratosis_follicularis": 2,
    "Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis": 2,
    "Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis|not_provided": 1,
    "Keratosis_follicularis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Keratosis_follicularis|Acrokeratosis_verruciformis_of_Hopf": 1,
    "Keratosis_follicularis|ATP2A2-related_disorder|not_provided": 1,
    "not_provided|Keratosis_follicularis|Darier_disease|_acral_hemorrhagic_type": 1,
    "Darier_disease|_segmental|not_provided": 1,
    "ATP2A2-related_disorder|not_provided": 3,
    "not_provided|not_specified|Acrokeratosis_verruciformis_of_Hopf|Keratosis_follicularis": 1,
    "Darier_disease|_segmental": 1,
    "ATP2A2-related_disorder|not_specified|Keratosis_follicularis|Acrokeratosis_verruciformis_of_Hopf|not_provided": 1,
    "not_provided|not_specified|Keratosis_follicularis": 1,
    "not_specified|Keratosis_follicularis": 1,
    "Ferguson-Bonni_neurodevelopmental_syndrome": 4,
    "RAD9B-related_disorder": 3,
    "Joubert_syndrome_13": 27,
    "not_specified|Joubert_syndrome_13": 1,
    "not_provided|Joubert_syndrome_13": 1,
    "Joubert_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_13|Inborn_genetic_diseases": 4,
    "Joubert_syndrome_13|not_provided|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|TCTN1-related_disorder": 2,
    "not_specified|not_provided|Joubert_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_13|not_provided": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Developmental_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_13|TCTN1-related_disorder": 1,
    "not_provided|Joubert_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_13|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_13|Global_developmental_delay|Typical_Joubert_syndrome_MRI_findings": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_13": 8,
    "TCTN1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 4,
    "not_specified|Joubert_syndrome_13|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "TCTN1-related_disorder": 4,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_13": 1,
    "not_provided|not_specified|TCTN1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "TCTN1-related_disorder|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Joubert_syndrome_13": 3,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_13": 1,
    "Joubert_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_13": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_13|TCTN1-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_13": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Joubert_syndrome_13": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_13|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Joubert_syndrome_13|TCTN1-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_13|not_specified|not_provided": 1,
    "TCTN1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "TCTN1-related_disorder|not_specified|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_13": 1,
    "Inborn_genetic_diseases|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "not_specified|Meckel-Gruber_syndrome|Joubert_syndrome": 5,
    "Hypertrophic_cardiomyopathy_10": 163,
    "not_provided|Hypertrophic_cardiomyopathy_10": 9,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_10|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_10": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10": 12,
    "not_specified|Hypertrophic_cardiomyopathy_10|not_provided": 2,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|not_specified": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_10|not_provided|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 13,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 17,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 4,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype": 1,
    "not_specified|MYL2-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype": 8,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Congenital_heart_disease|Primary_familial_hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 13,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|not_provided": 2,
    "Hypertrophic_cardiomyopathy_10|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_10|MYL2-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_and_heart_failure|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10": 8,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|Cardiomyopathy": 3,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 2,
    "Hypertrophic_cardiomyopathy_10|not_specified|Cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_10": 6,
    "MYL2-related_disorder|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1S|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy_10|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiovascular_phenotype|MYL2-related_disorder|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|not_provided": 3,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_10|Congestive_heart_failure": 1,
    "Hypertrophic_cardiomyopathy_10|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 3,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_10|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|not_specified|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "not_specified|MYL2-related_disorder|Hypertrophic_cardiomyopathy_10": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|MYL2-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10": 1,
    "Hypertrophic_cardiomyopathy_10|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_10|not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_10": 1,
    "not_specified|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|MYL2-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_10|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 3,
    "MYL2-related_disorder|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Premature_ventricular_contraction|Death_in_infancy": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiomyopathy|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_10|Congestive_heart_failure": 1,
    "Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|not_specified": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYL2-related_disorder|Death_in_early_adulthood|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_10|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_10|not_provided|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10": 2,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_10|Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Myopathy|_myofibrillar|_12|_infantile-onset|_with_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy_10|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_10|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_10|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_10|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_10|Congestive_heart_failure": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_10|MYL2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_10|MYL2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_10|Familial_isolated_restrictive_cardiomyopathy": 1,
    "CUX2-related_disorder": 26,
    "CUX2-related_disorder|not_provided": 11,
    "Developmental_and_epileptic_encephalopathy|_67|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_67": 46,
    "not_provided|CUX2-related_disorder": 11,
    "Developmental_and_epileptic_encephalopathy|_67|CUX2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_67": 7,
    "CUX2-related_disorder|Developmental_and_epileptic_encephalopathy|_67|not_provided": 1,
    "Inborn_genetic_diseases|Hypertrophic_cardiomyopathy|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_67|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|CUX2-related_disorder": 2,
    "Russell-Silver_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CUX2-related_disorder|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_67": 1,
    "CUX2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_67": 3,
    "Intellectual_disability|not_provided|Inborn_genetic_diseases|CUX2-related_disorder": 1,
    "not_provided|CUX2-related_disorder|Developmental_and_epileptic_encephalopathy|_67": 1,
    "Familial_myelofibrosis": 1,
    "SH2B3-related_disorder|not_provided": 2,
    "SH2B3-related_disorder": 4,
    "Thrombocythemia_1|not_specified": 1,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Inborn_genetic_diseases": 2,
    "SH2B3-related_disorder|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Thrombocytosis": 1,
    "not_provided|SH2B3-related_disorder": 4,
    "Primary_myelofibrosis": 5,
    "Primary_myelofibrosis|Thrombocythemia_1|Hepatoblastoma|not_provided|Hereditary_cancer": 1,
    "not_provided|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Thrombocythemia_1|Primary_myelofibrosis": 2,
    "not_specified|not_provided|SH2B3-related_disorder": 1,
    "not_provided|Thrombocythemia_1|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Primary_myelofibrosis": 2,
    "Spinocerebellar_ataxia_type_2": 11,
    "Spinocerebellar_ataxia_type_2|not_provided|not_specified": 2,
    "not_provided|ATXN2-related_disorder": 1,
    "ATXN2-related_disorder|not_specified|not_provided": 1,
    "ATXN2-related_disorder": 8,
    "ATXN2-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia_type_2|not_specified": 3,
    "Amyotrophic_lateral_sclerosis|Spinocerebellar_ataxia_type_2": 1,
    "Parkinson_disease|_late-onset|ATXN2-related_disorder": 1,
    "not_specified|Spinocerebellar_ataxia_type_2|not_provided": 2,
    "not_provided|Spinocerebellar_ataxia_type_2|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|ATXN2-related_disorder": 1,
    "ALDH2-related_disorder|not_provided": 3,
    "ALDH2-related_disorder": 1,
    "Alcohol_sensitivity|_acute|not_provided|ALDH2-related_disorder": 1,
    "Alcohol_sensitivity|_acute": 1,
    "not_provided|ALDH2-related_disorder": 1,
    "ALDH2-related_disorder|AMED_syndrome|_digenic|Alcohol_sensitivity|_acute|Alcohol_dependence|SUBLINGUAL_NITROGLYCERIN|_SUSCEPTIBILITY_TO_POOR_RESPONSE_TO|ESOPHAGEAL_CANCER|_ALCOHOL-RELATED|_SUSCEPTIBILITY_TO|Susceptibility_to_hangover|ethanol_response_-_Toxicity": 1,
    "Neurocardiofaciodigital_syndrome": 6,
    "HECTD4-related_disorder": 19,
    "not_specified|HECTD4-related_disorder": 1,
    "Neurodevelopmental_disorder_with_seizures|_spasticity|_and_complete_or_partial_agenesis_of_the_corpus_callosum": 11,
    "HECTD4-related_disorder|not_specified": 1,
    "See_cases|Neurodevelopmental_disorder_with_seizures|_spasticity|_and_complete_or_partial_agenesis_of_the_corpus_callosum": 1,
    "Neurodevelopmental_disorder_with_seizures|_spasticity|_and_complete_or_partial_agenesis_of_the_corpus_callosum|not_specified": 1,
    "not_provided|HECTD4-related_disorder": 1,
    "HECTD4-related_disorder|not_provided": 1,
    "Noonan_syndrome_1|Metachondromatosis|LEOPARD_syndrome_1": 7,
    "LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1": 16,
    "Noonan_syndrome_1|not_provided|Metachondromatosis|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|RASopathy": 1,
    "Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1": 3,
    "LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis": 21,
    "Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1": 12,
    "Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|Metachondromatosis|LEOPARD_syndrome_1": 10,
    "LEOPARD_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|RASopathy|not_provided|Noonan_syndrome|See_cases": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|RASopathy": 1,
    "Noonan_syndrome|not_provided|Metachondromatosis|Juvenile_myelomonocytic_leukemia|not_specified": 1,
    "Noonan_syndrome|not_provided|Metachondromatosis|Juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome|not_provided|RASopathy|not_specified": 1,
    "PTPN11-related_disorder": 3,
    "Metachondromatosis": 17,
    "not_specified|not_provided|LEOPARD_syndrome_1|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_1|Metachondromatosis": 1,
    "PTPN11-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|not_specified|RASopathy|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|RASopathy": 1,
    "LEOPARD_syndrome_1": 2,
    "RASopathy|LEOPARD_syndrome_1|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome": 1,
    "RASopathy|LEOPARD_syndrome_1|Cardiovascular_phenotype|Metachondromatosis|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1": 1,
    "RASopathy|Cardiovascular_phenotype|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|PTPN11-related_disorder|not_specified|RASopathy": 1,
    "not_provided|Ewing_sarcoma": 1,
    "RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|Cardiovascular_phenotype|not_provided|Noonan_syndrome|Noonan_syndrome_1|RASopathy": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia": 1,
    "Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|RASopathy|not_provided|Noonan_syndrome": 1,
    "PTPN11-related_disorder|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_specified|RASopathy|Cardiovascular_phenotype|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_3": 1,
    "Noonan_syndrome|not_provided|Noonan_syndrome_1|RASopathy|Metachondromatosis|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|PTPN11-related_disorder|Cardiovascular_phenotype|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|RASopathy": 1,
    "Noonan_syndrome_1|RASopathy": 5,
    "PTPN11-related_disorder|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|See_cases": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_1|LEOPARD_syndrome_1|RASopathy|not_provided|See_cases": 1,
    "PTPN11-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_provided|RASopathy|Noonan_syndrome": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|not_provided|Noonan_syndrome_1|Noonan_syndrome_3|RASopathy": 1,
    "not_provided|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|Non-immune_hydrops_fetalis|Short_stature|Abnormal_cardiovascular_system_morphology": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Dysplastic_pulmonary_valve|Tricuspid_regurgitation|Patent_ductus_arteriosus|Atrial_septal_defect|_ostium_secundum_type|Failure_to_thrive|Right_ventricular_hypertrophy|Cardiovascular_phenotype|PTPN11-related_disorder|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|B_lymphoblastic_leukemia_lymphoma|_no_ICD-O_subtype|Lymphoma|PTPN11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|RASopathy|Noonan_syndrome|Noonan_syndrome_3": 1,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Noonan_syndrome|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|Noonan_syndrome_3": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|RASopathy|not_provided|Noonan_syndrome": 1,
    "PTPN11-related_disorder|not_provided|Noonan_syndrome|Noonan_syndrome_1|Noonan_syndrome_3|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Juvenile_myelomonocytic_leukemia|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_provided|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|not_provided|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_1|not_provided|RASopathy": 1,
    "Noonan_syndrome|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|LEOPARD_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|RASopathy|not_provided|Noonan_syndrome|Intellectual_disability|Vascular_disorder": 1,
    "RASopathy|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1": 1,
    "Malignant_neoplastic_disease|PTPN11-related_disorder|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "RASopathy|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "RASopathy|Juvenile_myelomonocytic_leukemia|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_1|RASopathy|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|Noonan_syndrome|RASopathy": 1,
    "PTPN11-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|LEOPARD_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_3": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|RASopathy": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Noonan_syndrome|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|not_provided|RASopathy|Juvenile_myelomonocytic_leukemia": 1,
    "Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|RASopathy": 3,
    "RASopathy|Metachondromatosis": 3,
    "PTPN11-related_disorder|Cardiovascular_phenotype": 3,
    "not_provided|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|RASopathy": 1,
    "Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|Metachondromatosis|LEOPARD_syndrome_1|RASopathy|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_provided|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Noonan_syndrome|Autism_spectrum_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|RASopathy": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_3|not_provided|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_1|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|not_provided|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis": 1,
    "Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|PTPN11-related_disorder|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|RASopathy|PTPN11-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_specified|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Microcephaly|Pectus_excavatum|Brachycephaly|Ptosis|Global_developmental_delay|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_3|Hypertrophic_cardiomyopathy": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Noonan_syndrome|not_provided|Inborn_genetic_diseases|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome_1": 2,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|PTPN11-related_disorder|not_specified": 1,
    "Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|Metachondromatosis|LEOPARD_syndrome_1|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|Metachondromatosis|LEOPARD_syndrome_1|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_1|not_provided": 1,
    "LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Noonan_syndrome_1|Metachondromatosis|RASopathy|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|RASopathy": 2,
    "RASopathy|Noonan_syndrome|LEOPARD_syndrome_1|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Metachondromatosis|Noonan_syndrome_1|not_provided": 1,
    "RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1|Cardiovascular_phenotype|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy": 1,
    "Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|RASopathy|Cardiovascular_phenotype": 2,
    "Noonan_syndrome|not_provided|PTPN11-related_disorder|RASopathy": 1,
    "LEOPARD_syndrome_1|RASopathy|not_provided": 1,
    "RASopathy|PTPN11-related_disorder|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_specified|not_provided|RASopathy": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|not_provided|RASopathy": 1,
    "PTPN11-related_disorder|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_specified|not_provided|RASopathy": 1,
    "LEOPARD_syndrome_1|RASopathy": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder": 1,
    "not_provided|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|RASopathy": 1,
    "Noonan_syndrome|LEOPARD_syndrome_1|Noonan_syndrome_1|Proportionate_short_stature|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|RASopathy": 1,
    "PTPN11-related_disorder|not_provided|RASopathy|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1": 1,
    "Cardiovascular_phenotype|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|not_specified|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "RASopathy|Noonan_syndrome_1|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Noonan_syndrome": 8,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|RASopathy|Noonan_syndrome": 1,
    "RASopathy|not_provided|Neurofibromatosis-Noonan_syndrome": 1,
    "RASopathy|Noonan_syndrome_1": 1,
    "Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1": 1,
    "RASopathy|Cardiovascular_phenotype|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|not_provided|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|RASopathy|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|PTPN11-related_disorder|RASopathy": 1,
    "Cardiovascular_phenotype|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|not_provided|RASopathy|Noonan_syndrome": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|not_specified|Metachondromatosis|Noonan_syndrome_1|RASopathy|LEOPARD_syndrome_1": 1,
    "not_specified|Noonan_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "RASopathy|LEOPARD_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|CBL-related_disorder|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|not_specified|RASopathy": 1,
    "Noonan_syndrome_1|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Neurodevelopmental_abnormality|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|LEOPARD_syndrome_1|Noonan_syndrome_1|Cleft_lip/palate|Metachondromatosis|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy": 1,
    "Noonan_syndrome|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_1|not_provided|PTPN11-related_disorder": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|not_provided|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|RASopathy|Noonan_syndrome|Noonan_syndrome_3": 1,
    "PTPN11-related_disorder|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|LEOPARD_syndrome_1|Metachondromatosis|not_provided|RASopathy": 1,
    "Metachondromatosis|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|LEOPARD_syndrome_1|RASopathy": 1,
    "not_provided|RASopathy|Noonan_syndrome|not_specified": 1,
    "not_provided|Noonan_syndrome|not_specified": 2,
    "Noonan_syndrome|not_provided|not_specified|Juvenile_myelomonocytic_leukemia|Metachondromatosis": 1,
    "RASopathy|Noonan_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|Early_T_cell_progenitor_acute_lymphoblastic_leukemia|not_provided|RASopathy|LEOPARD_syndrome_1|Non-immune_hydrops_fetalis|Noonan_syndrome|Noonan_syndrome_1|Metachondromatosis": 1,
    "Noonan_syndrome_1|not_provided|Noonan_syndrome|Noonan_syndrome_3|RASopathy": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_provided|Intellectual_disability": 1,
    "not_specified|not_provided|Metachondromatosis|Cardiovascular_phenotype|RASopathy": 1,
    "Cardio-facio-cutaneous_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|not_specified|not_provided|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Hereditary_cancer-predisposing_syndrome|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|Thrombocytopenia|Abnormal_bleeding": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|Cardiovascular_phenotype|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|RASopathy|not_provided|Noonan_syndrome|See_cases": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_3": 1,
    "not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|LEOPARD_syndrome_1|not_specified|Noonan_syndrome_1|Noonan_syndrome|Metachondromatosis|PTPN11-related_disorder": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_specified|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|PTPN11-related_disorder|Cardiovascular_phenotype|RASopathy|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|Metachondromatosis|Juvenile_myelomonocytic_leukemia|Noonan_syndrome_1|LEOPARD_syndrome_1|not_specified|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|not_provided|RASopathy": 1,
    "Juvenile_myelomonocytic_leukemia|RASopathy|not_specified|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|RASopathy|Metachondromatosis|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|not_specified|not_provided|RASopathy": 2,
    "RASopathy|Cardiovascular_phenotype|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|RASopathy": 1,
    "not_provided|PTPN11-related_disorder": 1,
    "Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_specified|not_provided|RASopathy|PTPN11-related_disorder|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|RASopathy|Juvenile_myelomonocytic_leukemia": 1,
    "Cardiovascular_phenotype|not_specified|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|RASopathy": 1,
    "Cardiovascular_phenotype|RASopathy|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|not_specified": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|PTPN11-related_disorder": 1,
    "Noonan_syndrome_1|Metachondromatosis|Cardiovascular_phenotype|not_specified|RASopathy|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_specified|not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Neurofibroma": 1,
    "Acute_megakaryoblastic_leukemia_in_down_syndrome|Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|RASopathy": 1,
    "Cardiovascular_phenotype|RASopathy|PTPN11-related_disorder|not_provided|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1": 1,
    "RASopathy|Cardiovascular_phenotype|PTPN11-related_disorder": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "not_provided|Intellectual_disability|RASopathy|Noonan_syndrome_1": 1,
    "RASopathy|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|not_provided": 1,
    "Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_provided|RASopathy": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|RASopathy": 2,
    "Metachondromatosis|Noonan_syndrome_1|not_provided|LEOPARD_syndrome_1": 1,
    "Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_specified|RASopathy": 1,
    "not_specified|Noonan_syndrome_1": 1,
    "LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|not_provided": 1,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|not_specified|not_provided|RASopathy": 1,
    "PTPN11-related_disorder|not_specified|RASopathy|not_provided|LEOPARD_syndrome_1|Noonan_syndrome_1|Noonan_syndrome_with_multiple_lentigines": 1,
    "not_provided|LEOPARD_syndrome_1|Noonan_syndrome_with_multiple_lentigines|RASopathy": 1,
    "PTPN11-related_disorder|not_specified|LEOPARD_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|not_provided|RASopathy|LEOPARD_syndrome_1|Noonan_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|RASopathy|Noonan_syndrome_with_multiple_lentigines": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis|RASopathy": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|Noonan_syndrome|RASopathy": 1,
    "Astrocytic_tumor|Noonan_syndrome_and_Noonan-related_syndrome|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Noonan_syndrome_1|not_provided|Noonan_syndrome|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|RASopathy|not_provided|Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|Noonan_syndrome|RASopathy|Abnormal_facial_shape|Strabismus|Short_stature": 1,
    "Noonan_syndrome|LEOPARD_syndrome_1|Noonan_syndrome_1|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Metachondromatosis|Juvenile_myelomonocytic_leukemia|PTPN11-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|Cardiovascular_phenotype|LEOPARD_syndrome_1|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|not_provided|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|not_provided|RASopathy|LEOPARD_syndrome_1|Noonan_syndrome_1|Intellectual_disability|_mild|Scoliosis|Abnormal_facial_shape|Cafe-au-lait_spot|Specific_learning_disability": 1,
    "RASopathy|not_specified|Noonan_syndrome": 1,
    "Noonan_syndrome_1|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|RASopathy|not_provided": 1,
    "Microcephaly|Short_stature|Depressed_nasal_ridge|Epicanthus|Abnormal_pinna_morphology|Wide_nasal_bridge|Abnormal_cardiovascular_system_morphology|Cardiovascular_phenotype|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|not_provided|Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Juvenile_myelomonocytic_leukemia|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome|Intellectual_disability": 1,
    "Neurodevelopmental_disorder|PTPN11-related_disorder|Cardiovascular_phenotype|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|not_provided|RASopathy|Noonan_syndrome": 1,
    "LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy": 1,
    "Embryonal_rhabdomyosarcoma": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Noonan_syndrome": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|RASopathy|LEOPARD_syndrome_1|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Non-immune_hydrops_fetalis|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|not_provided|RASopathy|LEOPARD_syndrome_1|Noonan_syndrome_1|Noonan_syndrome_3|See_cases": 1,
    "PTPN11-related_disorder|Noonan_syndrome|Noonan_syndrome_with_multiple_lentigines|LEOPARD_syndrome_1|Noonan_syndrome_1|not_provided|RASopathy|Noonan_syndrome_3": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy|LEOPARD_syndrome_1|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy": 1,
    "not_specified|Noonan_syndrome|PTPN11-related_disorder|not_provided|Noonan_syndrome_1": 1,
    "Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|not_specified|RASopathy": 1,
    "Duane_retraction_syndrome|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|not_specified|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_provided|RASopathy": 1,
    "LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|Noonan_syndrome": 1,
    "Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis|not_specified|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|PTPN11-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|not_provided|RASopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Noonan_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Noonan_syndrome_1|LEOPARD_syndrome_1|Juvenile_myelomonocytic_leukemia|Metachondromatosis": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|PTPN11-related_disorder|Noonan_syndrome_1|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Metachondromatosis|not_specified|not_provided|RASopathy": 1,
    "PTPN11-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiovascular_phenotype|Metachondromatosis|Juvenile_myelomonocytic_leukemia|LEOPARD_syndrome_1|Noonan_syndrome_1|not_provided|not_specified|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|Premature_ventricular_contraction|RASopathy": 1,
    "not_specified|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1": 1,
    "Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1": 1,
    "PTPN11-related_disorder|not_provided|Cardiovascular_phenotype|RASopathy": 1,
    "Juvenile_myelomonocytic_leukemia|Metachondromatosis|Noonan_syndrome_1|LEOPARD_syndrome_1|See_cases|RASopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|RASopathy|Juvenile_myelomonocytic_leukemia|Metachondromatosis|LEOPARD_syndrome_1|Noonan_syndrome_1": 1,
    "Metachondromatosis|Noonan_syndrome_with_multiple_lentigines|not_specified|Noonan_syndrome|PTPN11-related_disorder": 1,
    "PTPN11-related_disorder|not_specified|LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1": 1,
    "LEOPARD_syndrome_1|Metachondromatosis|Noonan_syndrome_1|not_provided": 1,
    "Metachondromatosis|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome": 3,
    "Noonan_syndrome_1|LEOPARD_syndrome_1|Metachondromatosis": 5,
    "Metachondromatosis|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_with_multiple_lentigines|Metachondromatosis|Noonan_syndrome": 2,
    "not_provided|Metachondromatosis|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome": 1,
    "LEOPARD_syndrome_1|not_provided|Noonan_syndrome_1|Metachondromatosis": 1,
    "not_provided|LEOPARD_syndrome_1|Noonan_syndrome_1|Metachondromatosis": 1,
    "not_provided|Noonan_syndrome_1|LEOPARD_syndrome_1|Metachondromatosis": 1,
    "RPH3A-related_condition": 3,
    "RPH3A-related_condition|not_provided": 1,
    "OAS1-related_disorder|not_provided": 3,
    "not_provided|Pulmonary_alveolar_proteinosis_with_hypogammaglobulinemia": 1,
    "OAS1-related_disorder": 7,
    "Pulmonary_alveolar_proteinosis_with_hypogammaglobulinemia": 7,
    "not_specified|Pulmonary_alveolar_proteinosis_with_hypogammaglobulinemia|not_provided": 1,
    "not_provided|OAS1-related_disorder": 2,
    "not_specified|not_provided|OAS1_polymorphism|OAS1-related_disorder": 1,
    "Pulmonary_alveolar_proteinosis_with_hypogammaglobulinemia|not_provided": 2,
    "not_specified|OAS1-related_disorder": 1,
    "not_specified|OAS1-related_disorder|not_provided": 1,
    "OAS1_polymorphism": 1,
    "not_specified|not_provided|OAS1-related_disorder": 1,
    "not_provided|OAS1-related_disorder|not_specified": 2,
    "Pulmonary_alveolar_proteinosis_with_hypogammaglobulinemia|not_specified|not_provided": 1,
    "OAS1-related_disorder|not_specified|not_provided": 1,
    "DDX54-related_disorder": 15,
    "DDX54-related_Neurodevelopmental_Disorder": 1,
    "Neurodevelopmental_delay|Intellectual_disability|Neurodevelopmental_disorders": 1,
    "DDX54-related_Neurodevelopment_Syndrome": 1,
    "not_provided|DDX54-related_disorder": 2,
    "Neurodevelopmental_delay|Seizure|Intellectual_disability|Neurodevelopmental_disorders": 2,
    "Multiple_renal_cysts|Reduced_renal_corticomedullary_differentiation|Renal_hypoplasia|Neurodevelopmental_disorders|DDX54-related_disorder": 1,
    "Neurodevelopmental_disorders|Intellectual_disability|Neurodevelopmental_delay": 2,
    "TBX5-related_disorder|not_provided": 1,
    "Holt-Oram_syndrome": 134,
    "Holt-Oram_syndrome|not_provided": 5,
    "not_provided|Holt-Oram_syndrome": 9,
    "not_provided|Holt-Oram_syndrome|not_specified": 1,
    "Holt-Oram_syndrome|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Aortic_valve_disease_2": 47,
    "Cardiovascular_phenotype|TBX5-related_disorder|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2": 545,
    "not_provided|Aortic_valve_disease_2": 17,
    "Aortic_valve_disease_2|Cardiovascular_phenotype": 37,
    "not_provided|Aortic_valve_disease_2|Cardiovascular_phenotype": 1,
    "not_provided|Aortic_valve_disease_2|Cardiovascular_phenotype|Holt-Oram_syndrome": 1,
    "Holt-Oram_syndrome|Cardiovascular_phenotype|Aortic_valve_disease_2": 2,
    "Cardiovascular_phenotype|Aortic_valve_disease_2|Holt-Oram_syndrome": 4,
    "Cardiovascular_phenotype|Aortic_valve_disease_2|not_provided": 1,
    "Cardiovascular_phenotype|Holt-Oram_syndrome": 2,
    "Holt-Oram_syndrome|Cardiovascular_phenotype": 2,
    "TBX5-related_disorder|Holt-Oram_syndrome|Aortic_valve_disease_2|Cardiovascular_phenotype": 1,
    "not_provided|Holt-Oram_syndrome|Aortic_valve_disease_2|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Aortic_valve_disease_2|Cardiovascular_phenotype": 1,
    "not_provided|Aortic_valve_disease_2|Holt-Oram_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Atrial_septal_defect|_ostium_secundum_type|Mitral_regurgitation|Ventricular_septal_defect": 1,
    "Cardiovascular_phenotype|not_provided|Aortic_valve_disease_2": 4,
    "Holt-Oram_syndrome|not_specified|Aortic_valve_disease_2|Cardiovascular_phenotype": 1,
    "Aortic_valve_disease_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Holt-Oram_syndrome|Aortic_valve_disease_2": 1,
    "Holt-Oram_syndrome|Aortic_valve_disease_2|Cardiovascular_phenotype": 7,
    "not_provided|TBX5-related_disorder|Holt-Oram_syndrome|Aortic_valve_disease_2|Cardiovascular_phenotype": 1,
    "TBX5-related_disorder|Aortic_valve_disease_2": 2,
    "not_provided|not_specified|Aortic_valve_disease_2": 2,
    "Aortic_valve_disease_2|TBX5-related_disorder|Cardiovascular_phenotype": 1,
    "TBX5-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Aortic_valve_disease_2": 2,
    "Aortic_valve_disease_2|Cardiovascular_phenotype|Holt-Oram_syndrome": 2,
    "Holt-Oram_syndrome|Aortic_valve_disease_2": 6,
    "TBX5-related_disorder|Cardiovascular_phenotype|Aortic_valve_disease_2": 3,
    "Holt-Oram_syndrome|Aortic_valve_disease_2|not_provided|Cardiovascular_phenotype": 1,
    "Aortic_valve_disease_2|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|TBX5-related_disorder|not_provided": 1,
    "TBX5-related_disorder|not_provided|Aortic_valve_disease_2|Holt-Oram_syndrome": 1,
    "Cardiovascular_phenotype|Aortic_valve_disease_2|not_specified": 2,
    "Cardiovascular_phenotype|TBX5-related_disorder|not_provided|Aortic_valve_disease_2": 1,
    "not_provided|Holt-Oram_syndrome|Aortic_valve_disease_2|Cardiovascular_phenotype|not_specified": 1,
    "Aortic_valve_disease_2|Holt-Oram_syndrome|Cardiovascular_phenotype": 1,
    "Holt-Oram_syndrome|Aortic_valve_disease_2|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "TBX5-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Aortic_valve_disease_2|Holt-Oram_syndrome": 3,
    "not_provided|TBX5-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Aortic_valve_disease_2|Holt-Oram_syndrome": 1,
    "Cardiovascular_phenotype|Aortic_valve_disease_2|Holt-Oram_syndrome|Heart|_malformation_of": 1,
    "Holt-Oram_syndrome|Aortic_valve_disease_2|not_provided": 1,
    "Aortic_valve_disease_2|Holt-Oram_syndrome": 3,
    "Aortic_valve_disease_2|Primary_dilated_cardiomyopathy": 1,
    "Aortic_valve_disease_2|Holt-Oram_syndrome|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype": 1,
    "Aortic_valve_disease_2|not_provided": 20,
    "not_provided|Aortic_valve_disease_2|Holt-Oram_syndrome|Cardiovascular_phenotype": 2,
    "TBX5-related_disorder": 5,
    "not_provided|Holt-Oram_syndrome|Cardiovascular_phenotype|Aortic_valve_disease_2": 1,
    "Atrial_septal_defect_1|Holt-Oram_syndrome": 1,
    "Cardiovascular_phenotype|TBX5-related_disorder|not_provided": 1,
    "TBX5-related_disorder|Holt-Oram_syndrome": 1,
    "Aortic_valve_disease_2|Holt-Oram_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|TBX5-related_disorder|Holt-Oram_syndrome|Aortic_valve_disease_2": 1,
    "Cardiovascular_phenotype|Holt-Oram_syndrome|not_specified|Aortic_valve_disease_2|not_provided": 1,
    "Aortic_valve_disease_2|not_specified": 3,
    "Atrial_septal_defect|Thumb_deformity|Small_thenar_eminence|Clubbing_of_fingers|Abnormal_radial_ray_morphology|Blue_nevus": 1,
    "Aortic_valve_disease_2|not_provided|not_specified": 2,
    "not_specified|not_provided|Aortic_valve_disease_2|Cardiovascular_phenotype|Holt-Oram_syndrome": 1,
    "not_provided|TBX5-related_disorder|Aortic_valve_disease_2": 1,
    "TBX5-related_disorder|not_provided|Holt-Oram_syndrome": 1,
    "not_provided|TBX5-related_disorder|Cardiovascular_phenotype|Aortic_valve_disease_2|Holt-Oram_syndrome": 1,
    "Holt-Oram_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Aortic_valve_disease_2": 1,
    "not_specified|Holt-Oram_syndrome": 1,
    "Ulnar-mammary_syndrome": 274,
    "not_provided|Ulnar-mammary_syndrome": 23,
    "Ulnar-mammary_syndrome|not_provided": 7,
    "TBX3-related_disorder": 128,
    "TBX3-related_disorder|Inborn_genetic_diseases|Ulnar-mammary_syndrome": 7,
    "Ulnar-mammary_syndrome|TBX3-related_disorder": 52,
    "Ulnar-mammary_syndrome|Inborn_genetic_diseases": 8,
    "TBX3-related_disorder|Ulnar-mammary_syndrome": 20,
    "Inborn_genetic_diseases|not_provided|Ulnar-mammary_syndrome": 1,
    "not_provided|TBX3-related_disorder": 1,
    "Ulnar-mammary_syndrome|TBX3-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ulnar-mammary_syndrome": 8,
    "TBX3-related_disorder|Ulnar-mammary_syndrome|not_provided": 1,
    "Ulnar-mammary_syndrome|TBX3-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|TBX3-related_disorder|Ulnar-mammary_syndrome": 1,
    "TBX3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|TBX3-related_disorder|Ulnar-mammary_syndrome": 2,
    "Inborn_genetic_diseases|TBX3-related_disorder": 5,
    "Ulnar-mammary_syndrome|Inborn_genetic_diseases|TBX3-related_disorder": 4,
    "Eccrine_porocarcinoma": 1,
    "TBX3-related_disorder|Ulnar-mammary_syndrome|Inborn_genetic_diseases": 3,
    "TBX3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TBX3-related_disorder|not_provided": 3,
    "TBX3-related_disorder|not_provided|Ulnar-mammary_syndrome": 2,
    "Ulnar-mammary_syndrome|Obesity|not_specified|TBX3-related_disorder": 1,
    "Ulnar-mammary_syndrome|not_provided|not_specified": 1,
    "not_specified|Ulnar-mammary_syndrome|not_provided": 2,
    "not_provided|Ulnar-mammary_syndrome|TBX3-related_disorder": 1,
    "Ulnar-mammary_syndrome|TBX3-related_disorder|not_provided": 1,
    "Ulnar-mammary_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ulnar-mammary_syndrome|TBX3-related_disorder": 1,
    "Ulnar-mammary_syndrome|not_specified|not_provided": 1,
    "not_provided|TBX3-related_disorder|Inborn_genetic_diseases": 1,
    "Ulnar-mammary_syndrome|not_provided|TBX3-related_disorder": 1,
    ".|Intellectual_disability": 3,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided": 14,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.|not_provided": 2,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided|.": 4,
    "Intellectual_disability|.": 2,
    "MED13L-related_disorder|.|not_provided": 3,
    "Inborn_genetic_diseases|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.": 2,
    "Intellectual_disability|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 2,
    "not_provided|.|Intellectual_disability": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.": 9,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|MED13L-related_disorder|.": 1,
    "Inborn_genetic_diseases|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 7,
    "Impaired_intellectual_development_and_distinctive_facial_features_with_cardiac_defects": 2,
    "MED13L-related_disorder": 30,
    "MED13L-related_disorder|not_provided|.": 8,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|.": 5,
    "not_provided|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 8,
    ".|MED13L-related_disorder": 6,
    "MED13L-related_disorder|.|Inborn_genetic_diseases|Intellectual_disability": 1,
    ".|not_provided|MED13L-related_disorder": 1,
    "Inborn_genetic_diseases|MED13L-related_disorder": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|Inborn_genetic_diseases": 5,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided|Intellectual_disability": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|See_cases": 1,
    "MED13L-related_disorder|Inborn_genetic_diseases": 1,
    ".|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 6,
    "MED13L-related_disorder|not_provided|.|Inborn_genetic_diseases": 1,
    "not_provided|.|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 2,
    "MED13L-related_disorder|.": 8,
    "not_provided|MED13L-related_disorder|.": 4,
    "Inborn_genetic_diseases|not_provided|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.": 1,
    "not_provided|Inborn_genetic_diseases|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.": 1,
    "not_provided|.|MED13L-related_disorder": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|.": 1,
    "MED13L-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|.": 1,
    "not_specified|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 1,
    "See_cases|.": 1,
    "not_provided|Autism_spectrum_disorder|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|Marfanoid_habitus_and_intellectual_disability": 1,
    "MED13L-related_disorder|Inborn_genetic_diseases|not_provided|.|See_cases": 1,
    "MED13L-related_disorder|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided": 1,
    "MED13L-related_disorder|not_provided": 2,
    "MED13L-related_disorder|Inborn_genetic_diseases|.|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided": 1,
    "not_specified|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|MED13L-related_disorder|not_provided|.": 1,
    "MED13L-related_disorder|not_provided|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 2,
    ".|MED13L-related_disorder|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|.": 1,
    ".|Inborn_genetic_diseases|MED13L-related_disorder": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|MED13L-related_disorder": 1,
    "Kabuki-like_syndrome|not_provided|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 1,
    "Inborn_genetic_diseases|.|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome": 1,
    "MED13L-related_neurodevelopmental_disorder": 3,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder|.": 1,
    "not_provided|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_specified": 1,
    "Motor_delay|Delayed_speech_and_language_development|Strabismus|Vesicoureteral_reflux": 1,
    ".|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|MED13L-related_disorder|.|Inborn_genetic_diseases|not_provided": 1,
    "MED13L-related_disorder|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided|.": 1,
    "MED13L-related_disorder|not_provided|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.|Inborn_genetic_diseases": 2,
    "Intellectual_disability|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|not_provided": 1,
    "MED13L-related_disorder|.|Inborn_genetic_diseases|not_provided": 1,
    "MED13L-related_disorder|.|Inborn_genetic_diseases": 1,
    "MED13L-related_disorder|not_specified|.": 1,
    "not_provided|MED13L-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.|not_provided": 1,
    "not_provided|.|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|MED13L-related_disorder|.|not_provided": 1,
    "Impaired_intellectual_development_and_distinctive_facial_features_with_cardiac_defects|Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|.": 1,
    "MED13L-related_disorder|not_provided|.|not_specified": 1,
    "Cardiac_anomalies_-_developmental_delay_-_facial_dysmorphism_syndrome|Intellectual_disability": 1,
    "NOS1-related_disorder": 19,
    "NOS1-related_disorder|not_specified": 1,
    "NOS1-related_disorder|not_provided": 10,
    "not_provided|NOS1-related_disorder": 8,
    "not_provided|NOS1-related_disorder|not_specified": 1,
    "Pyloric_stenosis|_infantile_hypertrophic|_1": 1,
    "KSR2-related_disorder": 196,
    "not_provided|KSR2-related_disorder": 25,
    "not_provided|KSR2-related_disorder|not_specified": 2,
    "KSR2-related_disorder|not_provided": 20,
    "not_specified|KSR2-related_disorder": 7,
    "Hyperlipidemia|Type_2_diabetes_mellitus|Obesity|Diabetes_mellitus|Hypertensive_disorder|Class_III_obesity": 1,
    "not_provided|not_specified|KSR2-related_disorder": 1,
    "KSR2-related_disorder|not_provided|not_specified": 3,
    "KSR2-related_disorder|not_specified": 7,
    "KSR2-related_disorder|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2A|Charcot-Marie-Tooth_disease_axonal_type_2L": 8,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A": 10,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L": 126,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A": 3,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|not_provided": 7,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2L": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Inborn_genetic_diseases": 10,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2L": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2L": 5,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|HSPB8-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2L|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2L|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neuronopathy|_distal_hereditary_motor|_type_2A|Charcot-Marie-Tooth_disease_axonal_type_2L|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L|Inborn_genetic_diseases": 1,
    "HSPB8-related_disorder": 3,
    "HSPB8-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2L": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2A|Charcot-Marie-Tooth_disease_axonal_type_2L|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2A": 3,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2A|Charcot-Marie-Tooth_disease_axonal_type_2L": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Peripheral_neuropathy": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2L": 1,
    "Myopathy|_autophagic_vacuolar|_infantile-onset|Charcot-Marie-Tooth_disease_axonal_type_2L|Myopathy|_myofibrillar|_13|_with_rimmed_vacuoles": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Myopathy|_myofibrillar|_13|_with_rimmed_vacuoles": 1,
    "Distal_myopathy|.": 1,
    "Myopathy|_myofibrillar|_13|_with_rimmed_vacuoles": 4,
    "Neuronopathy|_distal_hereditary_motor|_type_2A|Charcot-Marie-Tooth_disease_axonal_type_2L|not_specified": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2L|Neuronopathy|_distal_hereditary_motor|_type_2A": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_2A|Myopathy|_myofibrillar|_13|_with_rimmed_vacuoles|HSPB8-related_neuromuscular_disorder": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|Myopathy|_myofibrillar|_13|_with_rimmed_vacuoles": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_2A|Charcot-Marie-Tooth_disease_axonal_type_2L|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2L|not_provided|Neuronopathy|_distal_hereditary_motor|_type_2A": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Distal_spinal_muscular_atrophy|Intellectual_disability|_autosomal_dominant_46": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Distal_spinal_muscular_atrophy": 1,
    "CIT-related_disorder": 11,
    "not_specified|CIT-related_disorder|not_provided": 1,
    "not_provided|CIT-related_disorder": 12,
    "Microcephaly_17|_primary|_autosomal_recessive": 23,
    "CIT-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "CIT-related_disorder|not_provided": 16,
    "Microcephaly_17|_primary|_autosomal_recessive|not_provided": 6,
    "Inborn_genetic_diseases|Microcephaly_17|_primary|_autosomal_recessive": 2,
    "Microcephaly_17|_primary|_autosomal_recessive|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Microcephaly_17|_primary|_autosomal_recessive": 2,
    "not_provided|Microcephaly_17|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|CIT-related_disorder|not_specified": 1,
    "not_provided|Microcephaly_17|_primary|_autosomal_recessive": 7,
    "Inborn_genetic_diseases|Microcephaly_17|_primary|_autosomal_recessive|not_provided": 1,
    "CIT-related_disorder|Microcephaly_17|_primary|_autosomal_recessive|not_specified|not_provided|Intellectual_disability": 1,
    "Microcephaly_17|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 2,
    "CIT-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|CIT-related_disorder": 1,
    "Autosomal_recessive_primary_microcephaly|Microcephaly_17|_primary|_autosomal_recessive": 2,
    "Autosomal_recessive_RNU4-2-related_neurodevelopmental_disorder": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_brain_anomalies|_distinctive_facies|_and_absent_language": 22,
    "Neurodevelopmental_disorder_with_hypotonia|_brain_anomalies|_distinctive_facies|_and_absent_language|not_provided": 1,
    "RNU4-2-associated_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia|_brain_anomalies|_distinctive_facies|_and_absent_language|RNU4-2-related_condition|not_provided": 1,
    "not_provided|RNU4-1-associated_neurodevelopmental_disorder": 1,
    "not_provided|COX6A1-related_disorder": 2,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_D|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_D|not_provided": 1,
    "COX6A1-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_42": 2,
    "Cardiomyopathy|_mitochondrial|Combined_oxidative_phosphorylation_deficiency_42": 1,
    "Coenzyme_q10_deficiency|_primary|_9": 1,
    "COQ5-related_disorder|not_provided": 1,
    "not_provided|COQ5-related_disorder": 2,
    "not_provided|Coenzyme_q10_deficiency|_primary|_9": 1,
    "COQ5-related_disorder": 3,
    "Deficiency_of_butyryl-CoA_dehydrogenase|not_provided": 23,
    "ACADS-related_disorder": 7,
    "not_specified|Deficiency_of_butyryl-CoA_dehydrogenase": 6,
    "Deficiency_of_butyryl-CoA_dehydrogenase|ACADS-related_disorder": 8,
    "ACADS-related_disorder|Inborn_genetic_diseases|not_provided|Deficiency_of_butyryl-CoA_dehydrogenase": 1,
    "ACADS-related_disorder|not_provided|Deficiency_of_butyryl-CoA_dehydrogenase": 4,
    "not_provided|Deficiency_of_butyryl-CoA_dehydrogenase": 33,
    "See_cases|Deficiency_of_butyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_butyryl-CoA_dehydrogenase|ACADS-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_butyryl-CoA_dehydrogenase": 2,
    "not_provided|Deficiency_of_butyryl-CoA_dehydrogenase|not_specified": 1,
    "not_provided|Deficiency_of_butyryl-CoA_dehydrogenase|ACADS-related_disorder": 2,
    "ACADS-related_disorder|Deficiency_of_butyryl-CoA_dehydrogenase": 4,
    "not_specified|Deficiency_of_butyryl-CoA_dehydrogenase|not_provided": 2,
    "Deficiency_of_butyryl-CoA_dehydrogenase|not_specified": 6,
    "not_specified|not_provided|Deficiency_of_butyryl-CoA_dehydrogenase": 2,
    "ACADS-related_disorder|Deficiency_of_butyryl-CoA_dehydrogenase|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Deficiency_of_butyryl-CoA_dehydrogenase": 1,
    "ACADS-related_disorder|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|See_cases|Deficiency_of_butyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_butyryl-CoA_dehydrogenase|not_provided|not_specified": 1,
    "not_provided|Type_2_diabetes_mellitus|Deficiency_of_butyryl-CoA_dehydrogenase": 1,
    "Deficiency_of_butyryl-CoA_dehydrogenase|See_cases": 1,
    "Deficiency_of_butyryl-CoA_dehydrogenase|not_specified|not_provided": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder": 1,
    "Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 3,
    "Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Monogenic_diabetes|not_provided": 1,
    "not_specified|HNF1A-related_disorder|Monogenic_diabetes": 1,
    "not_provided|HNF1A-related_disorder": 5,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus_type_1|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3": 40,
    "Maturity-onset_diabetes_of_the_young_type_3|not_provided": 4,
    "HNF1A-related_disorder|not_specified|Maturity-onset_diabetes_of_the_young_type_3|Nonpapillary_renal_cell_carcinoma|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20": 1,
    "HNF1A-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|HNF1A-related_disorder": 1,
    "HNF1A-related_disorder": 15,
    "Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus": 1,
    "not_provided|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1": 2,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3": 7,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3|not_specified|Nonpapillary_renal_cell_carcinoma": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3": 2,
    "Monogenic_diabetes|HNF1A-related_disorder|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_3": 29,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|not_provided": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3": 6,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|not_provided": 3,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 2,
    "Diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Nonpapillary_renal_cell_carcinoma|SERUM_HDL_CHOLESTEROL_LEVEL|_MODIFIER_OF|Maturity-onset_diabetes_of_the_young_type_3|Insulin_resistance|_susceptibility_to|Type_2_diabetes_mellitus": 1,
    "HNF1A-related_disorder|Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Clear_cell_carcinoma_of_kidney|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Chromophobe_renal_cell_carcinoma": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young": 3,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3": 4,
    "Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|not_provided|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Monogenic_diabetes": 1,
    "Monogenic_diabetes|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 3,
    "Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|HNF1A-related_disorder|not_specified|not_provided": 1,
    "HNF1A-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 3,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 2,
    "not_provided|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided|not_specified": 2,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes": 6,
    "Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|not_specified|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes|HNF1A-related_disorder|not_specified": 1,
    "not_specified|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 2,
    "not_specified|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "not_provided|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Nonpapillary_renal_cell_carcinoma": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 1,
    "HNF1A-related_disorder|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Nonpapillary_renal_cell_carcinoma": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young": 2,
    "Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF1A-related_disorder|not_provided": 1,
    "not_specified|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Ovarian_cancer|Maturity-onset_diabetes_of_the_young_type_3|not_provided|Nonpapillary_renal_cell_carcinoma": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 2,
    "not_specified|Diabetes_mellitus_type_1|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|HNF1A-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided": 1,
    "Type_2_diabetes_mellitus|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes": 4,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 3,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_provided|HNF1A-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|not_provided|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 3,
    "HNF1A-related_disorder|not_specified|not_provided|Monogenic_diabetes": 1,
    "HNF1A-related_disorder|Monogenic_diabetes": 3,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young": 14,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3": 2,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_provided": 2,
    "not_provided|Diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_provided": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|not_provided": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_provided": 3,
    "HNF1A-related_disorder|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Hepatic_adenomas|_familial": 1,
    "Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Type_1_diabetes_mellitus_20|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_provided|Monogenic_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_provided": 1,
    "not_provided|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_specified|not_provided": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_provided|HNF1A-related_disorder|Monogenic_diabetes|Diabetes_mellitus": 1,
    "not_provided|Monogenic_diabetes|HNF1A-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 1,
    "HNF1A-related_disorder|Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus_type_1": 1,
    "Monogenic_diabetes|HNF1A-related_disorder|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|not_provided|HNF1A-related_disorder|Monogenic_diabetes": 1,
    "not_provided|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|HNF1A-related_disorder": 1,
    "not_specified|not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3": 2,
    "Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3": 5,
    "Monogenic_diabetes|not_specified|Maturity_onset_diabetes_mellitus_in_young": 3,
    "not_provided|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Diabetes_mellitus": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1": 2,
    "HNF1A-related_disorder|Monogenic_diabetes|Hepatic_adenomas|_familial|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|not_provided|Type_1_diabetes_mellitus_20": 1,
    "Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|not_provided|Maturity_onset_diabetes_mellitus_in_young": 2,
    "Maturity-onset_diabetes_of_the_young_type_3|not_specified": 1,
    "not_provided|Type_1_diabetes_mellitus_20": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Hyperinsulinism_due_to_HNF1A_deficiency|not_provided": 1,
    "Monogenic_diabetes|HNF1A-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 5,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus": 1,
    "Monogenic_diabetes|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Type_1_diabetes_mellitus_20|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus_type_1|not_provided|Clear_cell_carcinoma_of_kidney|DiGeorge_syndrome": 1,
    "not_specified|not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Monogenic_diabetes|not_provided": 1,
    "Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "Monogenic_diabetes|not_specified|not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_provided|HNF1A-related_disorder|not_specified": 1,
    "not_specified|not_provided|Nonpapillary_renal_cell_carcinoma|Monogenic_diabetes": 1,
    "not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Type_1_diabetes_mellitus_20": 1,
    "not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|HNF1A-related_disorder": 1,
    "not_specified|Diabetes_mellitus_type_2|_susceptibility_to": 1,
    "not_provided|Nonpapillary_renal_cell_carcinoma|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF1A-related_disorder|not_specified|Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|not_specified": 1,
    "Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Type_1_diabetes_mellitus_20|not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 1,
    "not_specified|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Type_1_diabetes_mellitus_20|HNF1A-related_disorder": 1,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_specified|Monogenic_diabetes|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|not_provided|HNF1A-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Nonpapillary_renal_cell_carcinoma|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_3|not_specified": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20": 1,
    "not_specified|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|not_provided": 1,
    "not_specified|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|not_provided": 1,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|not_provided|not_specified|Diabetes_mellitus_type_1|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|not_provided": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young": 1,
    "HNF1A-related_disorder|not_provided|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|not_specified": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|not_specified|Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Nonpapillary_renal_cell_carcinoma": 1,
    "HNF1A-related_disorder|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|not_specified": 1,
    "Ovarian_cancer|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1": 1,
    "not_specified|Monogenic_diabetes|not_provided|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial": 1,
    "Monogenic_diabetes|HNF1A-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus": 1,
    "Type_1_diabetes_mellitus_20": 1,
    "Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Monogenic_diabetes|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|not_provided|Monogenic_diabetes": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|Insulin-resistant_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma": 1,
    "Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|not_specified|not_provided": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder|Monogenic_diabetes|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|not_specified|Maturity-onset_diabetes_of_the_young_type_1|not_provided": 1,
    "Monogenic_diabetes|Nonpapillary_renal_cell_carcinoma|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_3|not_specified": 1,
    "Type_1_diabetes_mellitus_20|not_provided|not_specified": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|HNF1A-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|HNF1A-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|HNF1A-related_disorder|not_provided": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_provided|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|HNF1A-related_disorder|not_specified": 1,
    "Symphalangism_affecting_the_proximal_phalanx_of_the_4th_finger|Monogenic_diabetes|Reduced_delayed_hypersensitivity|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Breast_carcinoma": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_3|Nonpapillary_renal_cell_carcinoma|Hepatic_adenomas|_familial|Type_2_diabetes_mellitus|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|HNF1A-related_disorder|Monogenic_diabetes": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Diabetes_mellitus_type_1": 1,
    "Monogenic_diabetes|not_specified|Maturity-onset_diabetes_of_the_young_type_3|not_provided|HNF1A-related_disorder": 1,
    "Monogenic_diabetes|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes|not_provided": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|HNF1A-related_disorder|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "HNF1A-related_disorder|Diabetes_mellitus_type_1|Nonpapillary_renal_cell_carcinoma|Type_1_diabetes_mellitus_20|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|not_provided": 1,
    "Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|not_provided": 1,
    "Monogenic_diabetes|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "Maturity-onset_diabetes_of_the_young_type_3|Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|Monogenic_diabetes": 1,
    "Diabetes_mellitus_type_1|Maturity-onset_diabetes_of_the_young_type_3|Type_1_diabetes_mellitus_20|Type_2_diabetes_mellitus|Hepatic_adenomas|_familial|Nonpapillary_renal_cell_carcinoma|Monogenic_diabetes|not_provided": 1,
    "Diabetes_mellitus_type_1|Type_1_diabetes_mellitus_20|Hepatic_adenomas|_familial|Maturity-onset_diabetes_of_the_young_type_3|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|Ovarian_cancer|not_specified|not_provided": 1,
    "Monogenic_diabetes|not_specified|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_3|Gestational_diabetes": 1,
    "Type_2_diabetes_mellitus|not_provided|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_3": 1,
    "P2RX7-related_disorder": 1,
    "P2RX7-related_disorder|not_provided": 1,
    "ANAPC5-related_disorder": 1,
    "KDM2B-related_disorder": 39,
    "KDM2B-related_disorder|not_provided": 4,
    "not_provided|KDM2B-related_disorder": 4,
    "Hypotonia|Infantile_spasms|Microcephaly|Global_developmental_delay": 1,
    "KDM2B_Gene_Mutation": 1,
    "not_provided|KDM2B-related_syndrome": 1,
    "Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency": 128,
    "Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency|not_provided": 7,
    "not_provided|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2": 6,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2": 200,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|not_provided": 8,
    "not_provided|Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency": 3,
    "Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency|not_specified|not_provided": 3,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_1|Myopathy|_tubular_aggregate|_2|not_provided": 1,
    "not_provided|ORAI1-related_disorder|Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency": 1,
    "Myopathy|_tubular_aggregate|_2": 3,
    "not_specified|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2": 3,
    "ORAI1-related_disorder": 4,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|Inborn_genetic_diseases": 1,
    "ORAI1-related_disorder|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2": 1,
    "ORAI1-related_disorder|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|not_provided": 1,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency": 9,
    "Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency|not_specified": 2,
    "not_provided|Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency|not_specified": 1,
    "Myopathy_with_tubular_aggregates|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2": 1,
    "not_specified|Myopathy|_tubular_aggregate|_2|Combined_immunodeficiency_due_to_ORAI1_deficiency": 3,
    "not_specified|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|not_provided": 1,
    "Myopathy_with_tubular_aggregates|Myopathy|_tubular_aggregate|_2": 1,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|not_specified": 2,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|not_specified|not_provided": 3,
    "not_provided|Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_2|not_specified": 2,
    "Combined_immunodeficiency_due_to_ORAI1_deficiency|Myopathy|_tubular_aggregate|_1|Myopathy|_tubular_aggregate|_2": 1,
    "TMEM120B-related_disorder": 1,
    "SETD1B-related_disorder": 53,
    "Intellectual_developmental_disorder_with_seizures_and_language_delay": 105,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder_with_seizures_and_language_delay|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_seizures_and_language_delay": 10,
    "SETD1B-related_disorder|not_provided": 10,
    "Intellectual_developmental_disorder_with_seizures_and_language_delay|Inborn_genetic_diseases": 6,
    "not_provided|Intellectual_developmental_disorder_with_seizures_and_language_delay|Inborn_genetic_diseases": 1,
    "not_provided|SETD1B-related_disorder": 21,
    "Inborn_genetic_diseases|SETD1B-related_disorder": 9,
    "Intellectual_developmental_disorder_with_seizures_and_language_delay|not_provided": 3,
    "SETD1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|SETD1B-related_disorder": 3,
    "SETD1B-related_neurodevelopmental_disorder": 1,
    "Intellectual_developmental_disorder_with_seizures_and_language_delay|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder_with_seizures_and_language_delay": 5,
    "Inborn_genetic_diseases|not_provided|SETD1B-related_disorder": 1,
    "Neurodevelopmental_delay|not_provided|Intellectual_developmental_disorder_with_seizures_and_language_delay": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_seizures_and_language_delay": 1,
    "SETD1B-associated_disorder|not_provided": 1,
    "Hawkinsinuria|Tyrosinemia_type_III": 272,
    "Tyrosinemia_type_III|Hawkinsinuria": 34,
    "Hawkinsinuria": 5,
    "Tyrosinemia_type_III|Hawkinsinuria|not_provided": 6,
    "Hawkinsinuria|Tyrosinemia_type_III|Inborn_genetic_diseases": 2,
    "Global_developmental_delay|Hypertyrosinemia|Hypokinesia|Limb_dystonia|Spasticity|Abnormal_cerebral_white_matter_morphology": 1,
    "HPD-related_disorder|not_provided|Tyrosinemia_type_III|Hawkinsinuria|not_specified": 1,
    "Inborn_genetic_diseases|Tyrosinemia_type_III|Hawkinsinuria": 2,
    "HPD-related_disorder|Tyrosinemia_type_III|Hawkinsinuria": 1,
    "not_provided|Hawkinsinuria|Tyrosinemia_type_III": 1,
    "Tyrosinemia_type_III": 6,
    "Hawkinsinuria|Tyrosinemia_type_III|not_provided": 6,
    "Hawkinsinuria|Tyrosinemia_type_III|HPD-related_disorder": 2,
    "Hawkinsinuria|Tyrosinemia_type_III|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Hawkinsinuria|Tyrosinemia_type_III": 1,
    "Inborn_genetic_diseases|not_provided|Hawkinsinuria|Tyrosinemia_type_III|HPD-related_disorder": 1,
    "HPD-related_disorder|Hawkinsinuria|Tyrosinemia_type_III": 2,
    "not_specified|not_provided|Tyrosinemia_type_III|Hawkinsinuria": 1,
    "HPD-related_disorder|Tyrosinemia_type_III|Hawkinsinuria|not_provided": 1,
    "not_provided|Tyrosinemia_type_III|Hawkinsinuria": 1,
    "not_provided|not_specified|Hawkinsinuria|Hypertyrosinemia|Inborn_genetic_diseases": 1,
    "not_provided|Hypertyrosinemia|Hawkinsinuria": 2,
    "Spermatogenic_failure_33|Non-syndromic_male_infertility_due_to_sperm_motility_disorder|Male_infertility_with_teratozoospermia_due_to_single_gene_mutation": 2,
    "Spermatogenic_failure_33": 5,
    "CFAP251-related_disorder": 18,
    "CFAP251-related_disorder|not_provided": 3,
    "Spermatogenic_failure_33|CFAP251-related_disorder": 1,
    "not_specified|CFAP251-related_disorder": 1,
    "Spermatogenic_failure_33|Reduced_sperm_motility|multiple_morphologic_abnormalities_of_the_sperm_flagellum|dysplasia_of_the_mitochondrial_sheath": 1,
    "Spermatogenic_failure_33|Spermatogenic_failure_18": 1,
    "not_provided|CFAP251-related_disorder": 1,
    "BCL7A-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_64": 5,
    "not_provided|DIABLO-related_disorder": 2,
    "DIABLO-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_64": 1,
    "DIABLO-related_disorder": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_64|not_provided": 2,
    "not_specified|not_provided|DIABLO-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_64|Autosomal_dominant_nonsyndromic_hearing_loss": 1,
    "DIABLO-Related_Hearing_Loss": 1,
    "not_provided|not_specified|DIABLO-related_disorder": 1,
    "not_provided|DIABLO-related_disorder|not_specified": 1,
    "Mucopolysaccharidosis-plus_syndrome": 4,
    "VPS33A-related_disorder": 3,
    "Mucopolysaccharidosis-plus_syndrome|not_provided": 5,
    "not_provided|VPS33A-related_disorder": 4,
    "VPS33A-related_disorder|not_provided": 2,
    "not_provided|Mucopolysaccharidosis-plus_syndrome": 1,
    "Mucopolysaccharidosis-plus_syndrome|VPS33A-related_disorder": 1,
    "CLIP1-related_intellectual_disability": 2,
    "CLIP1-related_intellectual_disability|not_specified": 1,
    "CLIP1-related_disorder": 6,
    "not_specified|CLIP1-related_disorder|not_provided": 2,
    "ZCCHC8-related_disorder": 1,
    "ZCCHC8-related_disorder|not_provided": 4,
    "not_provided|ZCCHC8-related_disorder": 7,
    "ZCCHC8-related_disorder|not_specified|not_provided": 2,
    "not_provided|not_specified|ZCCHC8-related_disorder": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_5|not_provided|not_specified": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_5|not_provided": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_5": 4,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_5": 2,
    "Inherited_acute_myeloid_leukemia": 1,
    "Inherited_aplastic_anemia": 4,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_5|Dyskeratosis_congenita": 1,
    "Inherited_aplastic_anemia|not_provided": 1,
    "RSRC2-related_disorder": 1,
    "Strabismus|Global_developmental_delay|Autistic_behavior|Seizure|Myopia|Obesity": 1,
    "DENR-related_disorder": 5,
    "Spermatogenic_failure_67": 2,
    "Combined_oxidative_phosphorylation_defect_type_7": 27,
    "MTRFR-related_disorder": 2,
    "Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia": 34,
    "Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7": 35,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia": 7,
    "Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7": 3,
    "Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided": 2,
    "Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7|Hereditary_spastic_paraplegia_55|not_provided": 1,
    "Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7|not_specified": 2,
    "Hereditary_spastic_paraplegia_55": 5,
    "Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia": 1,
    "Abnormal_brain_morphology|Epileptic_encephalopathy|Hereditary_spastic_paraplegia_55|Combined_oxidative_phosphorylation_defect_type_7": 1,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_55|Combined_oxidative_phosphorylation_defect_type_7": 1,
    "Combined_oxidative_phosphorylation_defect_type_7|Hereditary_spastic_paraplegia_55": 1,
    "MTRFR-related_disorder|Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7": 1,
    "not_provided|Hereditary_spastic_paraplegia_55|Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7": 1,
    "Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7|MTRFR-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia|MTRFR-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "MTRFR-related_disorder|Hereditary_spastic_paraplegia|Spastic_paraplegia|Combined_oxidative_phosphorylation_defect_type_7": 1,
    "Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia|not_provided": 1,
    "MTRFR-related_disorder|Combined_oxidative_phosphorylation_defect_type_7|Spastic_paraplegia": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_7": 7,
    "Oculopharyngodistal_myopathy_4|not_specified": 1,
    "RILPL1-related_disorder": 1,
    "Oculopharyngodistal_myopathy_4": 2,
    "not_provided|Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "not_provided|EIF2B1-related_disorder": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Leukoencephalopathy_with_vanishing_white_matter_1": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_1|Vanishing_white_matter_disease|not_provided": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1|not_provided": 1,
    "not_specified|Leukoencephalopathy_with_vanishing_white_matter_1|not_provided": 1,
    "Vanishing_white_matter_disease|Microcephaly": 1,
    "not_provided|Joubert_syndrome_24|Meckel_syndrome|_type_8": 2,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8": 9,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24": 63,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Joubert_syndrome_24": 1,
    "Joubert_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_24|Meckel_syndrome|_type_8": 7,
    "TCTN2-related_disorder|Meckel_syndrome|_type_8|Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|not_specified|Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_24": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome": 5,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Inborn_genetic_diseases": 2,
    "Meckel_syndrome|_type_8": 2,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome": 6,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Meckel-Gruber_syndrome|Joubert_syndrome": 7,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_24|Meckel_syndrome|_type_8": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|TCTN2-related_disorder|Meckel_syndrome|_type_8|Inborn_genetic_diseases|Joubert_syndrome_24": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24|not_specified": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_24|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_24|Meckel_syndrome|_type_8": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24|not_provided|Inborn_genetic_diseases": 1,
    "TCTN2-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 5,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_8|Joubert_syndrome_24": 4,
    "Joubert_syndrome_24|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_24|Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|TCTN2-related_disorder": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_8|Joubert_syndrome_24|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_8|Joubert_syndrome_24": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_8|Inborn_genetic_diseases|Joubert_syndrome_24": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24": 6,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24|Inborn_genetic_diseases": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_8|Joubert_syndrome_24": 2,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Inborn_genetic_diseases|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|TCTN2-related_disorder|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_8": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided": 1,
    "Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Meckel_syndrome|_type_8": 1,
    "Joubert_syndrome_24|not_specified|not_provided|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_8|Joubert_syndrome_24|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_8|Inborn_genetic_diseases|Joubert_syndrome_24": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|not_specified|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Joubert_syndrome_24|Inborn_genetic_diseases|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|not_specified": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|TCTN2-related_disorder|not_provided|not_specified|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_24|Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_24|Meckel_syndrome|_type_8|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|not_provided|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|not_specified|not_provided|Joubert_syndrome_24": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24|not_provided": 1,
    "not_provided|Meckel_syndrome|_type_8|not_specified|Joubert_syndrome_24": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_8|Joubert_syndrome_24|not_specified": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases|Joubert_syndrome_24|Meckel_syndrome|_type_8": 1,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Inborn_genetic_diseases": 2,
    "not_specified|Meckel_syndrome|_type_8|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_24": 2,
    "Meckel_syndrome|_type_8|Joubert_syndrome": 1,
    "Joubert_syndrome_24": 4,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_24|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_8|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_24": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_24|Meckel_syndrome|_type_8|Inborn_genetic_diseases": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24|not_provided": 1,
    "TCTN2-related_disorder": 3,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders|not_provided|TCTN2-related_disorder|Meckel_syndrome|_type_6": 1,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided": 1,
    "not_specified|Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8": 1,
    "Joubert_syndrome_24|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_provided|TCTN2-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_8|Joubert_syndrome_24|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_24": 1,
    "Joubert_syndrome_24|Inborn_genetic_diseases|Meckel_syndrome|_type_8|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Meckel_syndrome|_type_8|Joubert_syndrome_24|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24|Microcephaly": 1,
    "Joubert_syndrome_24|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel_syndrome|_type_8|Joubert_syndrome|Meckel-Gruber_syndrome|Cutis_Laxa|_Recessive|not_specified|Joubert_syndrome_24": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Cutis_Laxa|_Recessive|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_8|Joubert_syndrome_24": 1,
    "Cutis_Laxa|_Recessive|Meckel_syndrome|_type_8|not_provided|Joubert_syndrome_24": 1,
    "Joubert_syndrome_24|Cutis_Laxa|_Recessive|not_provided|Meckel_syndrome|_type_8": 1,
    "not_provided|Meckel_syndrome|_type_8|Joubert_syndrome_24": 2,
    "Joubert_syndrome_24|Cutis_Laxa|_Recessive|Meckel_syndrome|_type_8|not_provided": 3,
    "Cutis_Laxa|_Recessive|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "not_provided|Cutis_Laxa|_Recessive": 2,
    "not_provided|Joubert_syndrome|Cutis_Laxa|_Recessive|Meckel-Gruber_syndrome": 1,
    "Cutis_Laxa|_Recessive|Cutis_laxa_with_osteodystrophy": 1,
    "Cutis_laxa_with_osteodystrophy": 88,
    "Joubert_syndrome|Cutis_Laxa|_Recessive|not_specified|Meckel-Gruber_syndrome|not_provided|Cutis_laxa_with_osteodystrophy": 1,
    "Inborn_genetic_diseases|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|not_provided|ALG9_congenital_disorder_of_glycosylation": 1,
    "not_provided|Inborn_genetic_diseases|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|ALG9_congenital_disorder_of_glycosylation": 1,
    "Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation|not_provided|Cutis_laxa": 1,
    "Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|ALG9_congenital_disorder_of_glycosylation": 2,
    "ATP6V0A2-related_disorder|ALG9_congenital_disorder_of_glycosylation": 4,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 3,
    "Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome": 10,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome": 1,
    "ATP6V0A2-related_disorder": 8,
    "Cutis_laxa|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|ALG9_congenital_disorder_of_glycosylation|not_provided": 1,
    "not_specified|ALG9_congenital_disorder_of_glycosylation": 7,
    "ATP6V0A2-related_disorder|not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|not_provided": 2,
    "Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|not_specified|not_provided|ATP6VOA2-related_disorder|Wrinkly_skin_syndrome": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Cutis_laxa_with_osteodystrophy": 2,
    "ALG9_congenital_disorder_of_glycosylation|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy": 1,
    "not_provided|ATP6V0A2-related_disorder|ALG9_congenital_disorder_of_glycosylation": 3,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|ALG9_congenital_disorder_of_glycosylation": 1,
    "not_provided|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|ALG9_congenital_disorder_of_glycosylation|not_specified": 1,
    "not_provided|not_specified|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation": 2,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|not_specified|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|not_provided|ATP6V0A2-related_disorder": 1,
    "Cutis_laxa_with_osteodystrophy|Inborn_genetic_diseases|Wrinkly_skin_syndrome|not_provided|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 4,
    "ALG9_congenital_disorder_of_glycosylation|not_specified|not_provided|Cutis_laxa_with_osteodystrophy|Inborn_genetic_diseases|Wrinkly_skin_syndrome": 1,
    "ALG9_congenital_disorder_of_glycosylation|Inborn_genetic_diseases|Cutis_laxa_with_osteodystrophy|not_provided": 1,
    "not_specified|not_provided|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome": 1,
    "Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation|not_provided": 1,
    "Inborn_genetic_diseases|ALG9_congenital_disorder_of_glycosylation": 6,
    "not_specified|ATP6V0A2-related_disorder|ALG9_congenital_disorder_of_glycosylation": 1,
    "ATP6V0A2-related_disorder|not_provided|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_specified|not_provided|Cutis_laxa_with_osteodystrophy": 1,
    "Inborn_genetic_diseases|ALG9_congenital_disorder_of_glycosylation|not_provided|Cutis_laxa_with_osteodystrophy": 3,
    "ALG9_congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided": 4,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Cutis_laxa_with_osteodystrophy|ATP6V0A2-related_disorder|ALG9_congenital_disorder_of_glycosylation": 1,
    "not_provided|not_specified|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 1,
    "Inborn_genetic_diseases|not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|not_specified|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Cutis_laxa_with_osteodystrophy|Inborn_genetic_diseases": 1,
    "Cutis_laxa_with_osteodystrophy|Inborn_genetic_diseases": 2,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|ATP6V0A2-related_disorder": 1,
    "not_specified|not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 4,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation": 1,
    "Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation|not_specified": 1,
    "not_specified|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome": 1,
    "ATP6V0A2-related_disorder|not_specified|not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 2,
    "Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation": 5,
    "Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|not_specified|ALG9_congenital_disorder_of_glycosylation": 1,
    "not_specified|ALG9_congenital_disorder_of_glycosylation|ATP6V0A2-related_disorder|not_provided": 1,
    "ATP6V0A2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy": 1,
    "ATP6VOA2-related_disorder": 1,
    "not_provided|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|not_specified": 1,
    "ALG9_congenital_disorder_of_glycosylation|ATP6V0A2-related_disorder|not_provided": 1,
    "not_provided|Cutis_laxa_with_osteodystrophy|ALG9_congenital_disorder_of_glycosylation": 2,
    "ALG9_congenital_disorder_of_glycosylation|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|not_provided|Inborn_genetic_diseases": 1,
    "ATP6V0A2-related_disorder|ALG9_congenital_disorder_of_glycosylation|not_specified|not_provided|Cutis_laxa_with_osteodystrophy": 1,
    "not_specified|ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|not_provided": 1,
    "Cutis_laxa_with_osteodystrophy|not_provided|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_Laxa|_Recessive|not_provided": 1,
    "not_provided|ALG9_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_provided|Cutis_laxa_with_osteodystrophy": 13,
    "Cutis_laxa_with_osteodystrophy|not_specified|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|ATP6V0A2-related_disorder|not_specified|Cutis_laxa_with_osteodystrophy|not_provided": 1,
    "Cutis_laxa_with_osteodystrophy|Wrinkly_skin_syndrome|not_provided|ALG9_congenital_disorder_of_glycosylation": 1,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|Cutis_laxa_with_osteodystrophy|Inborn_genetic_diseases|Wrinkly_skin_syndrome": 1,
    "Wrinkly_skin_syndrome": 1,
    "ATP6V0A2-related_disorder|Cutis_Laxa|_Recessive|not_provided|ALG9_congenital_disorder_of_glycosylation": 1,
    "not_specified|ALG9_congenital_disorder_of_glycosylation|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|Wrinkly_skin_syndrome|Cutis_laxa_with_osteodystrophy|not_provided": 1,
    "ALG9_congenital_disorder_of_glycosylation|Cutis_laxa_with_osteodystrophy|not_provided|Wrinkly_skin_syndrome": 1,
    "Cutis_laxa_with_osteodystrophy|not_provided": 4,
    "ALG9_congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "Cutis_laxa_with_osteodystrophy|ATP6V0A2-related_disorder": 1,
    "Cutis_laxa_with_osteodystrophy|Inborn_genetic_diseases|not_provided": 1,
    "DNAH10-related_disorder|not_specified": 2,
    "DNAH10-related_disorder": 42,
    "DNAH10-related_disorder|not_specified|not_provided": 2,
    "DNAH10-related_disorder|not_provided": 8,
    "not_specified|DNAH10-related_disorder": 3,
    "Spermatogenic_failure_56": 12,
    "not_provided|DNAH10-related_disorder": 11,
    "Male_infertility|not_provided": 1,
    "not_specified|Spermatogenic_failure_56": 1,
    "DNAH10-related_disorder|not_provided|not_specified": 1,
    "NCOR2-related_disorder": 80,
    "not_specified|NCOR2-related_disorder": 1,
    "NCOR2-related_disorder|not_specified": 6,
    "not_provided|NCOR2-related_disorder": 8,
    "NCOR2-related_disorder|not_provided": 3,
    "not_specified|not_provided|NCOR2-related_disorder": 1,
    "not_provided|SCARB1-related_disorder": 5,
    "SCARB1-related_disorder": 2,
    "SCARB1-related_disorder|not_provided": 7,
    "not_provided|HIGH_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_6|SCARB1-related_disorder": 1,
    "not_provided|HIGH_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_6": 1,
    "HIGH_DENSITY_LIPOPROTEIN_CHOLESTEROL_LEVEL_QUANTITATIVE_TRAIT_LOCUS_6|not_provided": 1,
    "DHX37-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 1,
    "46|XY_sex_reversal_11|not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 7,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 6,
    "not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|46|XY_sex_reversal_11": 6,
    "DHX37-related_disorder|not_provided": 16,
    "DHX37-related_disorder": 2,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Inborn_genetic_diseases": 2,
    "46|XY_sex_reversal_11": 6,
    "not_provided|DHX37-related_disorder": 12,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 1,
    "not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Inborn_genetic_diseases": 1,
    "not_provided|Disorder_of_sexual_differentiation|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|46|XY_sex_reversal_11|DHX37-related_disorder": 2,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Neurodevelopmental_delay|Seizure|Intellectual_disability|Neurodevelopmental_disorders": 1,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|46|XY_sex_reversal_11|not_provided": 2,
    "46|XY_sex_reversal_11|not_provided": 1,
    "46|XY_sex_reversal_11|DHX37-related_disorder": 1,
    "Inborn_genetic_diseases|46|XY_sex_reversal_11": 1,
    "DHX37-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|not_provided": 2,
    "not_provided|46|XY_sex_reversal_11|Abnormal_brain_morphology|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 1,
    "Inborn_genetic_diseases|46|XY_sex_reversal_11|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|not_provided": 1,
    "Neurodevelopmental_disorders|Seizure|Intellectual_disability|Neurodevelopmental_delay|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 1,
    "Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Intellectual_disability|Neurodevelopmental_delay|Neurodevelopmental_disorders|Abnormal_brain_morphology": 1,
    "not_provided|Male_infertility_with_spermatogenesis_disorder": 1,
    "Neurodevelopmental_delay|Cerebellar_dysplasia|Chorioretinal_lacunae|Abnormality_of_neuronal_migration|Polymicrogyria|Seizure|Coloboma_of_optic_nerve|Choreoathetosis|Intellectual_disability|Neurodevelopmental_disorders": 1,
    "DHX37-related_disorder|46|XY_sex_reversal_11|not_provided": 1,
    "not_provided|not_specified|DHX37-related_disorder": 1,
    "46|XY_sex_reversal_11|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies|Intellectual_disability|Neurodevelopmental_delay|Neurodevelopmental_disorders": 1,
    "not_provided|Inborn_genetic_diseases|46|XY_sex_reversal_11": 1,
    "Neurodevelopmental_delay|Intellectual_disability|Neurodevelopmental_disorders|not_provided|Neurodevelopmental_disorder_with_brain_anomalies_and_with_or_without_vertebral_or_cardiac_anomalies": 1,
    "TMEM132D-related_disorder": 24,
    "not_provided|TMEM132D-related_disorder": 2,
    "PIWIL1-related_disorder": 21,
    "ULK1-related_disorder|not_provided": 1,
    "not_provided|ULK1-related_disorder": 1,
    "ULK1-related_disorder": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 40,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 15,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 25,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_provided": 10,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|PUS1-related_disorder": 2,
    "not_provided|not_specified|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|PUS1-related_disorder": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_provided": 9,
    "PUS1-related_disorder|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_provided": 1,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 9,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 4,
    "PUS1-related_disorder|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_provided": 1,
    "not_provided|PUS1-related_disorder": 6,
    "Sideroblastic_anemia|Inborn_mitochondrial_myopathy|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_specified|Sideroblastic_anemia|Inborn_mitochondrial_myopathy": 1,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|Inborn_genetic_diseases": 1,
    "Inborn_mitochondrial_myopathy|Sideroblastic_anemia|PUS1-related_disorder|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|Inborn_genetic_diseases": 2,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_provided": 2,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_provided|not_specified": 2,
    "PUS1-related_disorder|not_provided": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|PUS1-related_disorder|not_provided": 2,
    "Inborn_mitochondrial_myopathy|Sideroblastic_anemia|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|not_provided|Inborn_genetic_diseases|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "not_provided|Inborn_genetic_diseases|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 3,
    "PUS1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_provided": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_specified": 2,
    "not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 3,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|PUS1-related_disorder": 2,
    "not_specified|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 1,
    "Inborn_mitochondrial_myopathy|Sideroblastic_anemia|not_provided|not_specified|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "not_provided|PUS1-related_disorder|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "Sideroblastic_anemia|Inborn_mitochondrial_myopathy|PUS1-related_disorder|not_provided": 1,
    "not_provided|Sideroblastic_anemia|Inborn_mitochondrial_myopathy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1|not_specified": 1,
    "Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "Inborn_genetic_diseases|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia": 1,
    "Sideroblastic_anemia|Inborn_mitochondrial_myopathy|PUS1-related_disorder|not_specified|not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "not_provided|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_1": 1,
    "EP400-related_disorder": 65,
    "EP400-related_disorder|not_provided": 9,
    "not_specified|EP400-related_disorder": 2,
    "not_provided|EP400-related_disorder": 6,
    "not_specified|not_provided|EP400-related_disorder": 1,
    "EP400-related_disorder|not_specified": 2,
    "EP400-associated_neurodevelopmental_disorder": 1,
    "EP400-related_disorder|not_specified|not_provided": 1,
    "GALNT9-related_disorder": 1,
    "FBRSL1-related_disorder": 4,
    "Syndromic_disease|FBRSL1-related_disorder": 1,
    "FBRSL1-associated_neurodevelopmental_syndrome|not_specified|not_provided": 1,
    "not_provided|P2RX2-related_disorder": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_41|not_provided": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_41": 9,
    "P2RX2-related_disorder|not_specified|not_provided": 3,
    "P2RX2-related_disorder|not_provided": 3,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_41|not_provided": 2,
    "P2RX2-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_41": 1,
    "not_provided|not_specified|P2RX2-related_disorder": 1,
    "P2RX2-related_disorder": 6,
    "not_specified|P2RX2-related_disorder|not_provided": 1,
    "not_provided|P2RX2-related_disorder|not_specified": 1,
    "P2RX2-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_41|not_provided|not_specified": 1,
    "POLE-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12": 26,
    "not_provided|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 14,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 40,
    "not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "not_provided|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|POLE_Exonuclease_Domain_Mutation|not_provided": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 8,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer|POLE-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_provided|not_specified": 1,
    "Familial_colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 11,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "POLE-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "POLE-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 2,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 26,
    "not_specified|not_provided|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12": 50,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 2,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified": 5,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|POLE-related_disorder|not_specified": 1,
    "not_provided|POLE-related_disorder": 7,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLE-related_disorder": 19,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 6,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 22,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 3,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome": 19,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "not_provided|POLE-related_polyposis_and_colorectal_cancer_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|not_provided": 6,
    "Familial_colorectal_cancer_type_X|POLE-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12": 112,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 3,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12": 32,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 3,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 6,
    "Polymerase_proofreading-related_adenomatous_polyposis|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Carcinoma_of_colon": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|POLE-related_disorder|not_provided": 4,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_colorectal_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 3,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided": 57,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12": 48,
    "not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12": 6,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12": 3,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|POLE-related_polyposis_and_colorectal_cancer_syndrome|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided": 62,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12": 6,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 5,
    "POLE-related_disorder": 5,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|Carcinoma_of_colon|POLE-related_disorder": 1,
    "not_specified|POLE-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 3,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 2,
    "Colorectal_cancer|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|not_provided": 4,
    "not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 2,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 16,
    "not_provided|POLE-related_polyposis_and_colorectal_cancer_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "not_provided|not_specified|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 13,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|POLE-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Polymerase_proofreading_associated_polyposis": 1,
    "Cancer_or_benign_tumor|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 4,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 4,
    "not_specified|not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 18,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Polymerase_proofreading-related_adenomatous_polyposis": 4,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 2,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 10,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|POLE-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X": 1,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|POLE-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 5,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer_type_X": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 9,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_specified|not_provided": 6,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_specified|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_colorectal_cancer_type_X|POLE-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Pediatric_high-grade_glioma": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder": 2,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Familial_colorectal_cancer|not_provided": 1,
    "POLE-related_disorder|not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 18,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_provided": 4,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Familial_colorectal_cancer|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|not_specified": 3,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|not_specified": 3,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_provided": 10,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "POLE-related_disorder|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|POLE-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer_type_X": 5,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided": 4,
    "not_specified|POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12": 2,
    "POLE-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12": 3,
    "Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Carcinoma_of_colon": 1,
    "not_provided|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Carcinoma_of_colon|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder": 3,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided": 3,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|POLE-related_polyposis_and_colorectal_cancer_syndrome|not_provided": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_provided|not_specified|POLE-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|not_specified": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 2,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|POLE-related_disorder": 2,
    "not_provided|not_specified|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_provided|not_specified|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12": 2,
    "POLE-related_disorder|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 5,
    "POLE-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified": 1,
    "Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|POLE-related_disorder|not_provided": 1,
    "not_specified|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Malignant_tumor_of_breast|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_specified|not_provided": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Carcinoma_of_colon": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 2,
    "not_provided|POLE-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10": 44,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Carcinoma_of_colon|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified": 2,
    "POLE-related_disorder|not_specified|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_specified|not_provided": 2,
    "not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Familial_colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12|Pediatric_high-grade_glioma|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|not_specified|Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided|Familial_colorectal_cancer_type_X": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer_susceptibility_12|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_disorder|not_provided": 11,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 2,
    "Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_specified|not_provided": 1,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|POLE-related_disorder": 2,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12": 2,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|not_provided|POLE-related_disorder": 1,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12": 3,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_provided": 1,
    "POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_specified|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X": 1,
    "POLE-related_disorder|not_specified|not_provided|Neuroepithelial_neoplasm|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12": 3,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_specified|POLE-related_polyposis_and_colorectal_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified|not_provided": 2,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|POLE-related_polyposis_and_colorectal_cancer_syndrome": 1,
    "not_specified|Carcinoma_of_colon|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 60,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified": 1,
    "not_provided|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|not_specified|POLE-related_disorder": 2,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|POLE-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|not_provided": 1,
    "not_specified|not_provided|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_specified|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_specified|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|not_provided": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|POLE-related_disorder|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_specified": 1,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 2,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "POLE-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Familial_colorectal_cancer_type_X|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|not_provided": 1,
    "POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Hereditary_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Malignant_tumor_of_breast": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified": 1,
    "not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|POLE-related_disorder|not_provided": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|POLE-related_polyposis_and_colorectal_cancer_syndrome": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "POLE-related_disorder|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_provided|not_specified": 1,
    "not_provided|Carcinoma_of_colon": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder": 1,
    "POLE-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|XFE_progeroid_syndrome|POLE-related_disorder|not_provided|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder": 1,
    "POLE-related_disorder|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Familial_colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_specified": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 2,
    "Colon_cancer|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12": 2,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_12|POLE-related_polyposis_and_colorectal_cancer_syndrome|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|POLE-related_polyposis_and_colorectal_cancer_syndrome|not_specified|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified": 1,
    "POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|not_provided": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 2,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Cystic_fibrosis-gastritis-megaloblastic_anemia_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_disorder|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|POLE-related_disorder": 1,
    "POLE-related_polyposis_and_colorectal_cancer_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Programmed_death_ligand-1_(PD-L1)_blocking_antibody_response": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "not_provided|not_specified|POLE-related_disorder": 1,
    "Familial_colorectal_cancer_type_X|POLE-related_disorder|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Colorectal_cancer|_susceptibility_to|_10|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 6,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLE-related_disorder|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_provided|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified": 2,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Familial_colorectal_cancer|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_polyposis_and_colorectal_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder|Hereditary_cancer|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Programmed_death_ligand-1_(PD-L1)_blocking_antibody_response|Endometrioid_adenocarcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Familial_colorectal_cancer_type_X|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Polymerase_proofreading_associated_polyposis|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|POLE-related_disorder": 1,
    "not_specified|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 23,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|not_provided": 1,
    "Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|not_provided|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Carcinoma_of_colon|not_provided": 2,
    "Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLE-related_disorder|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_12|not_specified|not_provided|POLE-related_disorder": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|POLE-related_disorder|POLE-related_polyposis_and_colorectal_cancer_syndrome": 1,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|POLE-related_polyposis_and_colorectal_cancer_syndrome|not_specified|not_provided": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided|POLE-related_disorder|not_specified|Colorectal_cancer|_susceptibility_to|_12": 1,
    "POLE-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_specified|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "POLE-related_disorder|Familial_colorectal_cancer|not_specified|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_12|Carcinoma_of_colon": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLE-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLE-related_disorder|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|_12|Colorectal_cancer|not_specified": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|POLE-related_disorder|Colorectal_cancer|_susceptibility_to|_12": 1,
    "Familial_colorectal_cancer|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intestinal_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "POLE-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|Hereditary_cancer-predisposing_syndrome|not_provided|POLE-related_disorder|Malignant_tumor_of_breast": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified": 1,
    "Facial_dysmorphism-immunodeficiency-livedo-short_stature_syndrome|Colorectal_cancer|_susceptibility_to|_12|Intrauterine_growth_retardation|_metaphyseal_dysplasia|_adrenal_hypoplasia_congenita|_genital_anomalies|_and_immunodeficiency|not_specified|not_provided": 1,
    "ANKLE2-related_disorder": 7,
    "ANKLE2-related_disorder|not_provided": 3,
    "not_specified|not_provided|ANKLE2-related_disorder": 1,
    "Microcephaly_16|_primary|_autosomal_recessive|not_provided": 8,
    "Microcephaly_16|_primary|_autosomal_recessive": 12,
    "ANKLE2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Microcephaly_16|_primary|_autosomal_recessive|not_provided|Microcephaly": 1,
    "Inborn_genetic_diseases|ANKLE2-related_disorder": 2,
    "not_provided|Microcephaly_16|_primary|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|ANKLE2-related_disorder|not_provided": 1,
    "Vanishing_white_matter_disease|Hypotonia|Intellectual_disability|Microcephaly_16|_primary|_autosomal_recessive": 1,
    "Microcephaly_16|_primary|_autosomal_recessive|Microcephaly": 1,
    "not_provided|ANKLE2-related_disorder": 2,
    "Microcephaly_16|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "See_cases|ANKLE2-related_disorder|not_provided": 1,
    "ANKLE2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|ANKLE2-related_disorder|Inborn_genetic_diseases|Microcephaly_16|_primary|_autosomal_recessive": 1,
    "ZMYM2-related_disorder": 22,
    "ZMYM2-related_disorder|not_provided": 4,
    "not_provided|ZMYM2-related_disorder": 3,
    "Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|not_provided": 3,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency_40": 1,
    "ZMYM2-related_disorder|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities": 5,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|not_provided": 1,
    "Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|not_provided": 1,
    "not_provided|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities": 2,
    "ZMYM2-related_neurodevelopmental_disorder_with_multiple_anomalies": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|Inborn_genetic_diseases": 1,
    "Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|not_provided|ZMYM2-related_disorder": 1,
    "Neurodevelopmental_abnormality|Seizure": 1,
    "Inborn_genetic_diseases|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities": 1,
    "not_provided|Neurodevelopmental-craniofacial_syndrome_with_variable_renal_and_cardiac_abnormalities|Inborn_genetic_diseases": 1,
    "Cataract_14_multiple_types": 153,
    "Zonular_Pulverulent_Cataract": 7,
    "Cataract_14_multiple_types|not_provided": 6,
    "not_provided|Cataract_14_multiple_types": 22,
    "Zonular_Pulverulent_Cataract|not_provided": 1,
    "GJA3-related_disorder": 6,
    "Inborn_genetic_diseases|Cataract_14_multiple_types": 4,
    "not_provided|GJA3-related_disorder|Cataract_14_multiple_types": 1,
    "GJA3-related_disorder|Inborn_genetic_diseases|Cataract_14_multiple_types": 1,
    "not_specified|not_provided|Cataract_14_multiple_types": 1,
    "Inborn_genetic_diseases|Cataract_14_multiple_types|GJA3-related_disorder": 1,
    "not_specified|Cataract_14_multiple_types|not_provided": 1,
    "Cataract_14_multiple_types|GJA3-related_disorder": 2,
    "GJA3-related_disorder|Cataract_14_multiple_types": 3,
    "not_provided|not_specified|Cataract_14_multiple_types": 1,
    "Cataract_14_multiple_types|Developmental_cataract": 2,
    "not_provided|Cataract_14_multiple_types|Inborn_genetic_diseases": 1,
    "Developmental_cataract|Cataract_14_multiple_types": 3,
    "Cataract_14_multiple_types|Developmental_cataract|Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome": 1,
    "Mutilating_keratoderma|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Hearing_loss|_autosomal_recessive|Keratitis_ichthyosis_and_deafness_syndrome|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "Keratitis_ichthyosis_and_deafness_syndrome|Nonsyndromic_Hearing_Loss|_Dominant|Hearing_loss|_autosomal_recessive|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 5,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 6,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 12,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 3,
    "not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 3,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss": 1,
    "not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 2,
    "GJB2-related_disorder|not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Nonsyndromic_genetic_hearing_loss|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 20,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided": 1,
    "not_provided|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_specified": 1,
    "Nonsyndromic_genetic_hearing_loss|not_specified": 2,
    "GJB2-related_disorder|Rare_genetic_deafness|Inborn_genetic_diseases|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Mutilating_keratoderma|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Hearing_impairment": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided": 1,
    "GJB2-related_disorder|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hearing_impairment": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 15,
    "GJB2-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|not_provided": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 2,
    "Rare_genetic_deafness|Hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 2,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Nonsyndromic_genetic_hearing_loss|not_provided": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_genetic_hearing_loss|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|not_provided|GJB2-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "Monogenic_hearing_loss|GJB2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided": 1,
    "Hearing_loss|Mutilating_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided": 1,
    "GJB2-related_disorder|Hearing_loss|not_provided": 1,
    "Hearing_loss|Rare_genetic_deafness|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "Rare_genetic_deafness|Hearing_loss|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Hearing_impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A": 7,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome|not_provided": 1,
    "Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss": 1,
    "not_specified|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided|Ear_malformation": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|not_provided|GJB2-related_disorder": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|nonsyndromic_sensorineural_hearing_loss": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 1,
    "Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 4,
    "not_provided|not_specified|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|not_provided": 1,
    "not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 1,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_genetic_hearing_loss": 1,
    "GJB2-related_disorder|Nonsyndromic_Deafness|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|not_provided": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Mutilating_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided": 1,
    "Hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|GJB2-related_disorder|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|not_specified|not_provided": 1,
    "Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided": 1,
    "Hearing_loss|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "Rare_genetic_deafness|Hearing_loss|Intellectual_disability|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 3,
    "Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_12|not_specified": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 2,
    "not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 3,
    "not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Progressive_sensorineural_hearing_impairment": 1,
    "Rare_genetic_deafness|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided": 1,
    "not_specified|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Hearing_loss|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|not_specified|Hearing_impairment": 1,
    "Rare_genetic_deafness|Hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|not_specified": 2,
    "Hearing_loss|Sensorineural_hearing_loss_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Monogenic_hearing_loss|Hearing_loss|Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Hearing_loss|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Monogenic_hearing_loss|Rare_genetic_deafness|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_impairment": 1,
    "not_specified|Hearing_impairment|not_provided|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss": 1,
    "CREBBP-related_disorder|Rare_genetic_deafness|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_provided|Autism_spectrum_disorder": 1,
    "GJB2-related_disorder|Hearing_loss|Rare_genetic_deafness|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|not_provided|nonsyndromic_sensorineural_hearing_loss|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 2,
    "Rare_genetic_deafness|Hearing_impairment|GJB2-related_disorder|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Rare_genetic_deafness|not_provided": 1,
    "Hearing_loss|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_Deafness|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Hearing_loss|Deafness|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_impairment|See_cases": 1,
    "Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Porokeratotic_adnexal_ostial_nevus|not_provided": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|nonsyndromic_sensorineural_hearing_loss|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|GJB2-related_disorder|Progressive_sensorineural_hearing_impairment|Rare_genetic_deafness|not_provided": 1,
    "GJB2-related_disorder|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|GJB2-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Nonsyndromic_genetic_hearing_loss": 1,
    "Hearing_loss|Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_provided|Autism_spectrum_disorder|Deafness|_digenic|_GJB2/GJB3|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "Rare_genetic_deafness|Monogenic_hearing_loss|Mutilating_keratoderma|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided|Sensorineural_hearing_loss_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_loss|_autosomal_recessive": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_provided|Hearing_impairment": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|Hereditary_palmoplantar_keratoderma|Nonsyndromic_Deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Palmoplantar_keratoderma-deafness_syndrome|Hearing_loss|_autosomal_recessive|Hearing_impairment": 1,
    "Nonsyndromic_genetic_hearing_loss|Hereditary_palmoplantar_keratoderma|Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Hearing_loss|_autosomal_recessive|Palmoplantar_keratoderma-deafness_syndrome": 1,
    "Palmoplantar_keratoderma-deafness_syndrome": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided|not_specified": 1,
    "Hearing_loss|Mutilating_keratoderma": 1,
    "not_provided|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|GJB2-related_disorder|not_provided": 1,
    "Rare_genetic_deafness|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified|not_provided": 1,
    "Mutilating_keratoderma|not_specified|not_provided": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "not_provided|Knuckle_pads|_deafness_AND_leukonychia_syndrome": 1,
    "not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|GJB2-related_disorder|Rare_genetic_deafness|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Hearing_loss": 1,
    "Mutilating_keratoderma|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|GJB2-related_disorder|Rare_genetic_deafness|Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_provided|Inborn_genetic_diseases|See_cases": 1,
    "Knuckle_pads|_deafness_AND_leukonychia_syndrome": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome": 1,
    "not_provided|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Ichthyosis_and_erythrokeratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Hearing_loss|Sensorineural_hearing_loss_disorder|not_provided|Mutilating_keratoderma": 1,
    "Hearing_loss|GJB2-related_disorder|Rare_genetic_deafness|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Hearing_impairment": 1,
    "GJB2-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Inborn_genetic_diseases": 1,
    "not_provided|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_genetic_hearing_loss|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness": 1,
    "GJB2-related_disorder|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_Deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_loss|_autosomal_recessive|Hearing_impairment": 1,
    "not_provided|not_specified|Hearing_impairment|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|not_provided|Rare_genetic_deafness": 2,
    "GJB2-related_disorder|Rare_genetic_deafness|Hearing_loss|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_Deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_impairment|See_cases": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|Monogenic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hearing_loss|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "Rare_genetic_deafness|GJB2-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|nonsyndromic_sensorineural_hearing_loss": 1,
    "not_provided|Monogenic_hearing_loss|Rare_genetic_deafness|not_specified|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_specified": 1,
    "Nonsyndromic_genetic_hearing_loss|not_specified|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided|Hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Sensorineural_hearing_loss_disorder|Nonsyndromic_genetic_hearing_loss|GJB2-related_disorder|Rare_genetic_deafness|Hearing_loss|_autosomal_recessive|Hereditary_palmoplantar_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_impairment": 1,
    "Rare_genetic_deafness|GJB2-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_genetic_hearing_loss": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Nonsyndromic_genetic_hearing_loss|nonsyndromic_sensorineural_hearing_loss|Hearing_loss": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hearing_loss|not_provided|Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss": 1,
    "Rare_genetic_deafness|not_provided|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Rare_genetic_deafness|Hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hearing_impairment": 1,
    "GJB2-related_disorder|Hearing_loss|Deafness|Rare_genetic_deafness|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hereditary_palmoplantar_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_104|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_loss|_autosomal_recessive|Deafness|_digenic|_GJB2/GJB6|Severe_sensorineural_hearing_impairment|Hearing_impairment|Bilateral_conductive_hearing_impairment|Bilateral_sensorineural_hearing_impairment|Ear_malformation|Intellectual_disability": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|not_provided|Hearing_impairment": 1,
    "GJB2-related_disorder|Rare_genetic_deafness|Hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_impairment": 1,
    "Inborn_genetic_diseases|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 1,
    "GJB2-related_disorder|not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Rare_genetic_deafness|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 2,
    "not_specified|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Rare_genetic_deafness|Mutilating_keratoderma|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Ichthyosis|_hystrix-like|_with_hearing_loss|Mutilating_keratoderma|not_provided": 1,
    "GJB2-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 1,
    "Rare_genetic_deafness|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "GJB2-related_disorder|not_specified|nonsyndromic_sensorineural_hearing_loss|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_specified|not_provided|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Mutilating_keratoderma|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "not_specified|Nonsyndromic_genetic_hearing_loss|Ichthyosis|_hystrix-like|_with_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Mutilating_keratoderma|not_provided|GJB2-related_disorder|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "GJB2-related_disorder|not_specified|not_provided|Nonsyndromic_Deafness|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A": 1,
    "Nonsyndromic_genetic_hearing_loss|Ichthyosis|_hystrix-like|_with_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 1,
    "Knuckle_pads|_deafness_AND_leukonychia_syndrome|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma|Hearing_loss|GJB2-related_disorder|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_104|Hereditary_palmoplantar_keratoderma|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hearing_loss|_autosomal_recessive|Ear_malformation|Hearing_impairment": 1,
    "Hearing_loss|Palmoplantar_keratoderma-deafness_syndrome|Mutilating_keratoderma|Knuckle_pads|_deafness_AND_leukonychia_syndrome|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Nonsyndromic_genetic_hearing_loss": 1,
    "GJB2-related_disorder": 2,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3A|not_specified": 1,
    "Ichthyosis|_hystrix-like|_with_hearing_loss|not_specified|Mutilating_keratoderma|Autosomal_dominant_keratitis-ichthyosis-hearing_loss_syndrome|Knuckle_pads|_deafness_AND_leukonychia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_dominant_nonsyndromic_hearing_loss_3A|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Palmoplantar_keratoderma-deafness_syndrome|not_provided": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome": 28,
    "Hidrotic_ectodermal_dysplasia_syndrome|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|not_specified": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|GJB6-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Inborn_genetic_diseases": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|GJB6-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B": 1,
    "not_provided|not_specified|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B": 2,
    "Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome": 13,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 2,
    "Hidrotic_ectodermal_dysplasia_syndrome|not_provided|GJB6-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A": 4,
    "not_provided|not_specified|Hidrotic_ectodermal_dysplasia_syndrome|GJB6-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "Nonsyndromic_Deafness|not_specified": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome": 6,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|not_specified": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Hidrotic_ectodermal_dysplasia_syndrome|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "not_provided|GJB6-related_disorder|Inborn_genetic_diseases": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|GJB6-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided": 1,
    "not_provided|GJB6-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|not_provided|GJB6-related_disorder": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Hidrotic_ectodermal_dysplasia_syndrome|not_provided": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B": 1,
    "not_provided|Hidrotic_ectodermal_dysplasia_syndrome|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Autosomal_dominant_nonsyndromic_hearing_loss_3B|not_provided": 1,
    "GJB6-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_3B|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1B|Hidrotic_ectodermal_dysplasia_syndrome|not_provided": 1,
    "Hidrotic_ectodermal_dysplasia_syndrome|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_3B|Autosomal_recessive_nonsyndromic_hearing_loss_1A|Autosomal_recessive_nonsyndromic_hearing_loss_1B|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_3B": 1,
    "CRYL1-related_disorder": 4,
    "not_specified|CRYL1-related_disorder": 1,
    "IFT88-related_disorder|not_provided": 11,
    "not_provided|IFT88-related_disorder": 5,
    "IFT88-related_disorder": 4,
    "not_provided|Rod-cone_dystrophy": 1,
    "MICU2-related_disorder|not_provided": 1,
    "not_provided|MICU2-related_disorder": 1,
    "MICU2-related_disorder": 1,
    "Multiple_synostoses_syndrome_3": 71,
    "Symphalangism-brachydactyly_syndrome": 26,
    "Multiple_synostoses_syndrome_3|not_provided": 7,
    "not_provided|Multiple_synostoses_syndrome_3|not_specified": 1,
    "FGF9-related_disorder|not_provided": 1,
    "not_provided|Multiple_synostoses_syndrome_3": 6,
    "not_specified|Multiple_synostoses_syndrome_3|not_provided": 1,
    "Multiple_synostoses_syndrome_3|not_specified|not_provided": 2,
    "FGF9-related_disorder": 1,
    "Symphalangism-brachydactyly_syndrome|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 347,
    "Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive": 2,
    "Sarcoglycanopathy": 14,
    "Sarcoglycanopathy|not_provided|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_provided|not_specified|SGCG-related_disorder|Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 41,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified": 3,
    "Sarcoglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Inborn_genetic_diseases": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_provided": 18,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_provided|not_specified": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified|not_provided": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified|SGCG-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified": 1,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|SGCG-related_disorder": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|SGCG-related_disorder|Sarcoglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Abnormality_of_the_musculature": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy|not_specified": 1,
    "SGCG-related_congenital_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|SGCG-related_disorder": 1,
    "SGCG-related_disorder": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "SGCG-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "SGCG-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided|Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy": 1,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Charlevoix-Saguenay_spastic_ataxia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Sarcoglycanopathy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified|Charlevoix-Saguenay_spastic_ataxia|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Charlevoix-Saguenay_spastic_ataxia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Sarcoglycanopathy|not_provided": 7,
    "Sarcoglycanopathy|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Charlevoix-Saguenay_spastic_ataxia|not_provided|Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "Sarcoglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C|not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "Charlevoix-Saguenay_spastic_ataxia": 858,
    "Limb-girdle_muscular_dystrophy|_recessive|Charlevoix-Saguenay_spastic_ataxia|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided": 32,
    "not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia": 23,
    "Limb-girdle_muscular_dystrophy|_recessive|Charlevoix-Saguenay_spastic_ataxia|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 2,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2C": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia": 21,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 173,
    "Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "SACS-related_disorder": 7,
    "Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia|Charcot-Marie-Tooth_disease": 1,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 135,
    "Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases": 6,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_specified": 7,
    "Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia": 6,
    "Charlevoix-Saguenay_spastic_ataxia|Autosomal_recessive_spastic_ataxia": 1,
    "Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 29,
    "not_specified|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 12,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_provided": 12,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 22,
    "Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_provided": 6,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified|not_provided": 2,
    "Charlevoix-Saguenay_spastic_ataxia|not_specified": 2,
    "Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 7,
    "Charlevoix-Saguenay_spastic_ataxia|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|not_specified": 1,
    "SACS-related_disorder|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 2,
    "not_provided|Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 3,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|not_specified": 1,
    "Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 3,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 2,
    "not_provided|Spastic_paraplegia|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 20,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_provided": 3,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_provided": 4,
    "not_provided|SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_specified": 1,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases": 3,
    "not_specified|Charlevoix-Saguenay_spastic_ataxia": 6,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_provided": 17,
    "not_provided|SACS-related_disorder|Spastic_paraplegia": 2,
    "Spastic_paraplegia|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia": 3,
    "Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia": 2,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|not_specified|not_provided|Spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia": 2,
    "not_provided|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 3,
    "not_specified|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|SACS-related_disorder": 5,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 4,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Autosomal_recessive_spastic_ataxia": 2,
    "not_provided|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|SACS-related_disorder|Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|not_provided|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 2,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Spastic_paraplegia": 8,
    "Spastic_paraplegia|SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|Spastic_paraplegia": 10,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_specified": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 6,
    "not_provided|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 2,
    "SACS-related_disorder|Spastic_paraplegia": 10,
    "Spastic_paraplegia|SACS-related_disorder|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|Spastic_paraplegia|not_specified": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_specified|Charlevoix-Saguenay_spastic_ataxia|not_provided": 1,
    "not_specified|SACS-related_disorder|Spastic_paraplegia": 1,
    "not_provided|not_specified|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "Spastic_paraplegia|not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia": 4,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 3,
    "not_specified|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 2,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 3,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia|Ataxia|_spastic|_childhood-onset|_autosomal_recessive|_with_optic_atrophy_and_intellectual_disability": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|not_specified|Spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|not_specified|Spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified|not_provided": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_specified|Spastic_paraplegia": 5,
    "Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_specified|not_provided": 1,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 2,
    "SACS-related_disorder|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia": 2,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Charcot-Marie-Tooth_disease": 1,
    "Autosomal_recessive_spastic_ataxia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|not_provided": 2,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_provided|Charlevoix-Saguenay_spastic_ataxia": 2,
    "Hereditary_spastic_paraplegia|not_specified|Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|SACS-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 2,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Intellectual_disability|Spastic_paraplegia|not_specified": 1,
    "not_specified|Charlevoix-Saguenay_spastic_ataxia|See_cases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 3,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|SACS-related_disorder": 1,
    "SACS-related_disorder|Spastic_paraplegia|not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 4,
    "not_provided|SACS-related_disorder|Hereditary_spastic_paraplegia|Spastic_paraplegia|Intellectual_disability|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia|not_provided": 3,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_provided|Hereditary_spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified": 1,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder": 2,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_specified|SACS-related_disorder": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|Spastic_paraplegia|not_provided": 3,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Inborn_genetic_diseases|not_provided": 2,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases": 4,
    "not_provided|Spastic_ataxia|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|SACS-related_disorder|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia": 3,
    "Spastic_paraplegia|not_provided|Intellectual_disability|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_specified|not_provided": 2,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "not_specified|SACS-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_specified|not_provided|Spastic_paraplegia": 2,
    "Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|Spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 2,
    "Charlevoix-Saguenay_spastic_ataxia|not_specified|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia|not_provided": 1,
    "SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia|not_specified|Spastic_paraplegia": 1,
    "SACS-related_disorder|Spastic_paraplegia|not_provided|not_specified": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|not_provided|Spastic_paraplegia|SACS-related_disorder": 2,
    "Spastic_paraplegia|SACS-related_disorder|Inborn_genetic_diseases": 1,
    "SACS-related_disorder|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified": 1,
    "not_provided|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|not_specified": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Hereditary_ataxia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Abnormal_brain_morphology": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|SACS-related_disorder|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|not_provided|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|Spastic_paraplegia|Hereditary_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_provided|not_specified": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|not_provided": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|Hereditary_spastic_paraplegia": 2,
    "SACS-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "SACS-related_disorder|Spastic_paraplegia|not_specified": 1,
    "SACS-related_disorder|Hereditary_spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia|not_provided|Hereditary_spastic_paraplegia": 1,
    "SACS-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Abnormal_central_motor_function|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|SACS-related_disorder": 1,
    "not_provided|not_specified|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|See_cases": 1,
    "Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|Spastic_paraplegia|not_provided": 1,
    "not_provided|Spastic_paraplegia|Spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|not_provided|SACS-related_disorder|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 2,
    "not_provided|See_cases|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Abnormal_central_motor_function|SACS-related_disorder|Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia|Abnormal_brain_morphology": 1,
    "SACS-related_disorder|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_specified|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "not_specified|Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 2,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|SACS-related_disorder|Inborn_genetic_diseases": 1,
    "Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|not_provided|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|SACS-related_disorder|not_provided|Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "SACS-related_disorder|Spastic_paraplegia|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|not_provided|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_provided": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|not_provided": 1,
    "SACS-related_disorder|Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_specified|not_provided|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_specified": 1,
    "Spastic_paraplegia|SACS-related_disorder|not_specified|Charlevoix-Saguenay_spastic_ataxia|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Charlevoix-Saguenay_spastic_ataxia|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia": 1,
    "Charlevoix-Saguenay_spastic_ataxia|not_provided|not_specified|Spastic_paraplegia|SACS-related_disorder": 1,
    "Spastic_paraplegia|not_provided|Charlevoix-Saguenay_spastic_ataxia|not_specified|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|SACS-related_disorder|Hereditary_spastic_paraplegia": 1,
    "not_provided|SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Hereditary_ataxia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|not_provided|SACS-related_disorder|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Inborn_genetic_diseases|Charlevoix-Saguenay_spastic_ataxia|not_provided|Spastic_paraplegia": 1,
    "not_provided|SACS-related_disorder|Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia": 1,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charlevoix-Saguenay_spastic_ataxia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Charlevoix-Saguenay_spastic_ataxia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|not_specified|Charlevoix-Saguenay_spastic_ataxia": 1,
    "Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome|not_provided": 1,
    "Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly": 2,
    "Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome|not_provided": 6,
    "Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 16,
    "MIPEP-related_disorder": 4,
    "not_provided|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 4,
    "Inborn_genetic_diseases|not_provided|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 1,
    "Cardiomyopathy|Left_ventricular_noncompaction|Floppy_infant|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 5,
    "not_provided|MIPEP-related_disorder": 6,
    "Inborn_genetic_diseases|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 4,
    "Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "MIPEP-related_disorder|not_provided": 2,
    "Cardiomyopathy|Left_ventricular_noncompaction|Floppy_infant|not_provided|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|MIPEP-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|MIPEP-related_disorder": 1,
    "Lethal_left_ventricular_non-compaction-seizures-hypotonia-cataract-developmental_delay_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "SPATA13-related_disorder": 21,
    "SPATA13-related_disorder|not_specified": 1,
    "not_specified|SPATA13-related_disorder": 1,
    "Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 42,
    "Seckel_syndrome|Primary_Microcephaly|_Recessive": 3,
    "not_provided|Primary_Microcephaly|_Recessive|Seckel_syndrome": 2,
    "Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|not_provided": 4,
    "not_provided|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 6,
    "Seckel_syndrome|not_provided|Primary_Microcephaly|_Recessive": 2,
    "Seckel_syndrome_4|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 7,
    "Primary_Microcephaly|_Recessive|Seckel_syndrome": 2,
    "CENPJ-related_disorder": 7,
    "not_provided|CENPJ-related_disorder|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "CENPJ-related_disorder|Seckel_syndrome_4|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Seckel_syndrome_5": 3,
    "Seckel_syndrome_4|Inborn_genetic_diseases|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|Inborn_genetic_diseases|Seckel_syndrome_4|not_provided": 1,
    "CENPJ-related_disorder|Inborn_genetic_diseases|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|not_provided": 1,
    "Microcephaly_6|_primary|_autosomal_recessive": 14,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 40,
    "Seckel_syndrome|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_provided|not_specified": 1,
    "not_provided|Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4": 4,
    "Meniere_disease|not_provided|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "not_specified|Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 4,
    "not_provided|Seckel_syndrome_4": 3,
    "Seckel_syndrome_4|not_specified|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "not_provided|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4|not_provided": 5,
    "Seckel_syndrome_4|not_provided|not_specified|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "not_provided|Microcephaly_6|_primary|_autosomal_recessive|Microcephaly|Lissencephaly": 1,
    "Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|not_specified|not_provided": 5,
    "not_provided|Microcephaly_6|_primary|_autosomal_recessive": 6,
    "Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "Seckel_syndrome_4|not_provided|Microcephaly_6|_primary|_autosomal_recessive|not_specified": 2,
    "Seckel_syndrome_4": 5,
    "Primary_Microcephaly|_Recessive|Seckel_syndrome|not_provided|not_specified": 1,
    "CENPJ-related_disorder|not_provided": 1,
    "Primary_Microcephaly|_Recessive|Seckel_syndrome|not_provided": 2,
    "not_specified|not_provided|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 3,
    "Seckel_syndrome_4|Inborn_genetic_diseases|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 2,
    "Seckel_syndrome_4|not_provided|Meniere_disease|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "not_provided|CENPJ-related_disorder|Inborn_genetic_diseases": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|not_specified|Seckel_syndrome_4|not_provided": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_4|not_provided|CENPJ-related_disorder|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "CENPJ-related_disorder|Seckel_syndrome_4|Seckel_syndrome_1|not_specified|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 2,
    "CENPJ-related_disorder|Inborn_genetic_diseases|not_provided|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|not_provided": 2,
    "Seckel_syndrome_4|not_specified|Microcephaly_6|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|not_specified|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 2,
    "Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4|not_provided|not_specified": 1,
    "Seckel_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "CENPJ-related_disorder|not_specified|not_provided|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive": 2,
    "Microcephaly_6|_primary|_autosomal_recessive|not_specified|Inborn_genetic_diseases|Seckel_syndrome_4|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Seckel_syndrome_4|not_specified": 1,
    "not_provided|Primary_microcephaly|Intellectual_disability|_moderate|Perisylvian_polymicrogyria|Lissencephaly_type_3|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Seckel_syndrome_4|Autosomal_recessive_primary_microcephaly": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|not_provided|Seckel_syndrome_4|not_specified": 1,
    "CENPJ-related_disorder|Inborn_genetic_diseases|Seckel_syndrome_4|Microcephaly_6|_primary|_autosomal_recessive|not_provided|Meniere_disease": 1,
    "CENPJ-related_disorder|Inborn_genetic_diseases|not_specified|Seckel_syndrome_4|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|not_provided|CENPJ-related_disorder|Inborn_genetic_diseases|not_specified|Seckel_syndrome_4": 1,
    "Seckel_syndrome|Microcephaly_6|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|Seckel_syndrome_4": 1,
    "Primary_Microcephaly|_Recessive|Seckel_syndrome|not_provided|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|not_provided|Lissencephaly_type_3|Intellectual_disability|_moderate|Perisylvian_polymicrogyria|Primary_microcephaly": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|CENPJ-related_disorder|not_provided|Seckel_syndrome_4|not_specified": 1,
    "Microcephaly_6|_primary|_autosomal_recessive|Seckel_syndrome_4|not_specified|not_provided": 2,
    "not_specified|Microcephaly_6|_primary|_autosomal_recessive|CENPJ-related_disorder|not_provided": 1,
    "not_specified|not_provided|Seckel_syndrome_4|Seckel_syndrome_1|Microcephaly_6|_primary|_autosomal_recessive": 1,
    "not_provided|Microcephaly_6|_primary|_autosomal_recessive|Microcephaly_1|_primary|_autosomal_recessive": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4": 44,
    "not_provided|ATP8A2-related_disorder": 4,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4|ATP8A2-related_disorder|not_provided": 2,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4|not_provided": 4,
    "ATP8A2-related_disorder|not_provided": 3,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4": 8,
    "not_provided|not_specified|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4": 1,
    "ATP8A2-related_disorder": 2,
    "ATP8A2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|ATP8A2-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|ATP8A2-related_disorder": 1,
    "not_specified|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4|not_provided|Inborn_genetic_diseases": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_developmental_disorder_with_hypotonia_and_behavioral_abnormalities": 26,
    "CDK8-related_disorder": 5,
    "not_provided|CDK8-related_disorder": 1,
    "Heart|_malformation_of|Stillbirth|Ventriculomegaly|Congenital_diaphragmatic_hernia|Abnormal_facial_shape|Common_atrium|Ebstein_anomaly": 1,
    "Complex_neurodevelopmental_disorder_with_or_without_congenital_anomalies|Intellectual_developmental_disorder_with_hypotonia_and_behavioral_abnormalities": 1,
    "Intellectual_developmental_disorder_with_hypotonia_and_behavioral_abnormalities|not_provided": 2,
    "not_provided|Intellectual_developmental_disorder_with_hypotonia_and_behavioral_abnormalities": 1,
    "CDK8-related_disorder|not_provided": 2,
    "Intellectual_developmental_disorder_with_hypotonia_and_behavioral_abnormalities|Intellectual_disability": 1,
    "Hypotrichosis_12": 1,
    "Treacher_Collins_syndrome_2": 12,
    "POLR1D-related_disorder": 7,
    "Treacher_Collins_syndrome_2|not_provided": 3,
    "Treacher_Collins_syndrome_2|Treacher_Collins_syndrome": 1,
    "not_provided|POLR1D-related_disorder": 2,
    "not_provided|Treacher_Collins_syndrome_2": 2,
    "Maturity-onset_diabetes_of_the_young_type_4": 8,
    "PDX1-related_disorder": 15,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "Pancreatic_hypoplasia|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|not_provided|Diabetes_mellitus_type_2|_susceptibility_to": 1,
    "Pancreatic_hypoplasia": 5,
    "Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Type_2_diabetes_mellitus": 28,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Type_2_diabetes_mellitus": 3,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "not_specified|not_provided|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1": 2,
    "Type_2_diabetes_mellitus|Pancreatic_agenesis_1|Maturity-onset_diabetes_of_the_young_type_4|not_specified|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Type_2_diabetes_mellitus|not_provided": 2,
    "Pancreatic_agenesis_1|Maturity-onset_diabetes_of_the_young_type_4|Type_2_diabetes_mellitus|not_provided|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|Type_2_diabetes_mellitus|not_provided": 1,
    "Pancreatic_hypoplasia|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_4": 2,
    "Maturity_onset_diabetes_mellitus_in_young|PDX1-related_disorder|not_specified|not_provided": 1,
    "Diabetes_mellitus_type_2|_susceptibility_to|not_provided|PDX1-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|not_provided|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Type_2_diabetes_mellitus|Monogenic_diabetes": 1,
    "Familial_Monogenic_Diabetes_(Maturity_Onset_Diabetes_Of_The_Young_4)/Neonatal_Diabetes_Mellitus|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|PDX1-related_disorder|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Type_2_diabetes_mellitus|not_provided|Neonatal_diabetes_mellitus": 1,
    "Monogenic_diabetes|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Diabetes_mellitus_type_2|_susceptibility_to|Maturity-onset_diabetes_of_the_young_type_4|Type_2_diabetes_mellitus": 1,
    "Pancreatic_hypoplasia|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Pancreatic_agenesis_1|Maturity-onset_diabetes_of_the_young_type_4|Type_2_diabetes_mellitus": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|not_specified": 1,
    "not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|PDX1-related_disorder": 1,
    "not_provided|Pancreatic_hypoplasia": 1,
    "not_provided|PDX1-related_disorder": 2,
    "Maturity_onset_diabetes_mellitus_in_young|PDX1-related_disorder|not_provided": 2,
    "Maturity-onset_diabetes_of_the_young_type_4|Type_2_diabetes_mellitus|Pancreatic_agenesis_1": 1,
    "Type_2_diabetes_mellitus|Pancreatic_agenesis_1|Maturity-onset_diabetes_of_the_young_type_4|not_provided": 1,
    "Diabetes_mellitus_type_2|_susceptibility_to|Pancreatic_agenesis_1": 1,
    "Familial_Monogenic_Diabetes_(Maturity_Onset_Diabetes_Of_The_Young_4)/Neonatal_Diabetes_Mellitus": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|PDX1-related_disorder|not_provided|Pancreatic_agenesis_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "Pancreatic_agenesis_1|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "Pancreatic_agenesis_1": 2,
    "Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|Permanent_neonatal_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Pancreatic_agenesis_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|not_provided": 1,
    "Pancreatic_agenesis_1|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|not_provided": 1,
    "Type_2_diabetes_mellitus|Pancreatic_agenesis_1|Maturity-onset_diabetes_of_the_young_type_4|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|PDX1-related_disorder": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified|Neonatal_diabetes_mellitus|Diabetes_mellitus_type_2|_susceptibility_to|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "Pancreatic_hypoplasia|Monogenic_diabetes|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_4": 1,
    "Monogenic_diabetes|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|not_specified|not_provided|PDX1-related_disorder": 1,
    "Pancreatic_hypoplasia|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_4|PDX1-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_4|not_specified": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_4|Pancreatic_agenesis_1|not_provided|not_specified": 1,
    "Sirenomelia": 1,
    "not_provided|Anorectal_malformation": 1,
    "Acute_lymphoid_leukemia|Acute_myeloid_leukemia": 2,
    "FLT3-related_disorder": 3,
    "Myelodysplastic_syndrome_progressed_to_acute_myeloid_leukemia": 1,
    "not_provided|FLT3-related_disorder": 3,
    "FLT3-related_disorder|not_specified|not_provided": 1,
    "not_provided|FLT1-related_disorder": 1,
    "FLT1-related_disorder": 1,
    "not_provided|Keratosis_linearis-ichthyosis_congenita-sclerosing_keratoderma_syndrome": 1,
    "POMP-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Keratosis_linearis-ichthyosis_congenita-sclerosing_keratoderma_syndrome|Proteasome-associated_autoinflammatory_syndrome_2": 1,
    "not_provided|Keratosis_linearis-ichthyosis_congenita-sclerosing_keratoderma_syndrome|Proteasome-associated_autoinflammatory_syndrome_2": 1,
    "POMP-related_disorder|not_provided": 1,
    "Proteasome-associated_autoinflammatory_syndrome_2|Keratosis_linearis-ichthyosis_congenita-sclerosing_keratoderma_syndrome": 1,
    "Proteasome-associated_autoinflammatory_syndrome_2": 2,
    "not_provided|POMP-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|POMP-related_disorder": 1,
    "HMGB1-related_Developmental_delay_and_microcephaly": 1,
    "Brachyphalangy|_polydactyly|_and_tibial_aplasia/hypoplasia": 2,
    "HMGB1-related_disorder": 3,
    "HMGB1-associated_disorder": 1,
    "ALOX5AP-related_disorder": 3,
    "not_specified|ALOX5AP-related_disorder": 1,
    "Peters_plus_syndrome": 147,
    "Peters_plus_syndrome|Inborn_genetic_diseases": 11,
    "not_provided|Peters_plus_syndrome|not_specified": 2,
    "B3GLCT-related_disorder|not_specified|Peters_plus_syndrome": 2,
    "not_provided|Peters_plus_syndrome": 21,
    "Peters_plus_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Peters_plus_syndrome": 1,
    "not_specified|Peters_plus_syndrome|not_provided": 1,
    "Peters_plus_syndrome|not_provided": 9,
    "B3GLCT-related_disorder|Peters_plus_syndrome": 2,
    "Inborn_genetic_diseases|Peters_plus_syndrome": 3,
    "Peters_plus_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Peters_plus_syndrome": 5,
    "not_provided|not_specified|Peters_plus_syndrome": 1,
    "Peters_plus_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "B3GLCT-related_disorder|Inborn_genetic_diseases|not_provided|Peters_plus_syndrome": 1,
    "B3GLCT-related_disorder": 2,
    "not_specified|Peters_plus_syndrome": 1,
    "Peters_plus_syndrome|B3GLCT-related_disorder|not_provided": 1,
    "B3GLCT-related_disorder|not_specified|not_provided|Peters_plus_syndrome": 1,
    "B3GLCT-related_disorder|Peters_plus_syndrome|not_provided": 2,
    "not_provided|Peters_plus_syndrome|B3GLCT-related_disorder": 2,
    "not_provided|Peters_plus_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Cryptorchidism": 3,
    "Bilateral_cryptorchidism": 3,
    "RXFP2-related_disorder": 1,
    "not_specified|RXFP2-related_disorder": 1,
    "FRY-related_condition": 2,
    "not_specified|FRY-related_condition": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 110,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 218,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 10,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 72,
    "Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 18,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_specified|Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 19,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition": 50,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 191,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 210,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 107,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 164,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|not_specified|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 12,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 38,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 88,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 121,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 36,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 11,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 36,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 36,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 28,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 13,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 118,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 40,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 22,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 131,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 148,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 11,
    "BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 2,
    "Malignant_tumor_of_breast|not_specified|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 14,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 166,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 46,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 54,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 64,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 18,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 22,
    "Ovarian_cancer|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 18,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 218,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 3,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_serous_surface_papillary_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 9,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 92,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 118,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 2,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_pancreas": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 6,
    "BRCA2-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_cancer|_susceptibility_to|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 37,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 9,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 15,
    "Ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 24,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Fanconi_anemia_complementation_group_D1|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 66,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 5,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 151,
    "Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Esophageal_atresia/tracheoesophageal_fistula|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 3,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 8,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Infiltrating_duct_carcinoma_of_breast|Familial_cancer_of_breast|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 4,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 19,
    "Breast_neoplasm|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Medulloblastoma|Wilms_tumor_1|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 19,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 8,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 10,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 30,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 11,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 14,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 9,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 30,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_cancer|_susceptibility_to": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided|BRCA2-related_disorder": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 10,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 6,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 59,
    "Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 8,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 76,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 62,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|BRCA2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 8,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Familial_prostate_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_pancreas": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 6,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 11,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 15,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 19,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 17,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 6,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 8,
    "Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Malignant_tumor_of_pancreas|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Carcinoma_of_colon": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_neoplasm|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Rhabdomyosarcoma|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 5,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 4,
    "Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Carcinoma_of_pancreas": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 5,
    "Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 24,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_specified|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Multiple_myeloma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 8,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 5,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "BRCA2-related_disorder": 7,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 18,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 5,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 5,
    "Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 3,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 8,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 9,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 8,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 5,
    "Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 10,
    "not_specified|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|bilateral_breast_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 39,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast_neoplasm|Wilms_tumor_1|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 16,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 11,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 31,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 11,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 21,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 8,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "BRCA2-related_disorder|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 4,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 19,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 3,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 7,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|not_provided|not_specified": 1,
    "Prostate_cancer|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "Uterine_corpus_cancer|BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_D1": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 15,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 11,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Ovarian_neoplasm": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 14,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Carcinoma_of_colon|Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Gastric_cancer|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 5,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 21,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided": 3,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "not_specified|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "Gastric_cancer|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_colorectal_cancer_type_X|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 9,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_neoplasm": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 14,
    "Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Familial_cancer_of_breast|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 20,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 4,
    "Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_D1|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 9,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Neuroendocrine_tumor_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Familial_cancer_of_breast": 1,
    "Medulloblastoma|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 8,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Neuroblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hepatoblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_ductal_adenocarcinoma|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified": 3,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_cancer_predisposition": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Focal-onset_seizure|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 5,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|BRCA2-related_disorder|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Wilms_tumor_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 2,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Breast_neoplasm|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 7,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Wilms_tumor_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 6,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 3,
    "BRCA2-related_cancer_predisposition|EBV-positive_nodal_T-_and_NK-cell_lymphoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Wilms_tumor_1|Medulloblastoma|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|BRCA2-related_disorder|not_provided|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRCA2-related_disorder|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Familial_cancer_of_breast|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "not_provided|not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 11,
    "Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 9,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 9,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 11,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Wilms_tumor_1|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 8,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Gastric_cancer|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 6,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 7,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 15,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast": 4,
    "Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "BRCA2-related_cancer_predisposition|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Nephroblastoma|Familial_colorectal_cancer_type_X": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Endometrial_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Malignant_tumor_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast_neoplasm|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "not_provided|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 7,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Carcinoma_of_male_breast|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2": 1,
    "not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Familial_prostate_cancer|Wilms_tumor_1|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided": 2,
    "Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Familial_prostate_cancer|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Medulloblastoma|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 8,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 13,
    "Malignant_tumor_of_breast|Breast_neoplasm|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Breast_neoplasm|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Wilms_tumor_1|Glioma_susceptibility_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_disorder|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 5,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Cancer_or_benign_tumor|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Pancreatic_cancer|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_cancer": 2,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3": 1,
    "Gastric_cancer|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Fanconi_anemia|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_disorder": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 9,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Carcinoma_of_pancreas": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 3,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 5,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Wilms_tumor_1|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|BRCA2-related_cancer_predisposition|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Melanoma|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 6,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 8,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_neoplasm|not_specified": 1,
    "Chordoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Chordoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 9,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Ovarian_cancer|Breast_neoplasm|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 7,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Medulloblastoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Kabuki_syndrome_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 8,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_disorder": 2,
    "Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Prostate_cancer|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|not_provided|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Endometrial_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 10,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|BRCA2-related_disorder|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Polyposis_syndrome|_hereditary_mixed|_1": 1,
    "BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Fanconi_anemia_complementation_group_D1|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 8,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Gastric_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 6,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 4,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Prostate_cancer|not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 3,
    "Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_pancreas": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 3,
    "BRCA2-related_disorder|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_cancer|_susceptibility_to|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_pancreatic_carcinoma|Familial_colorectal_cancer_type_X|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm": 6,
    "not_specified|BRCA2-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 2,
    "BRCA2-related_cancer_predisposition|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Glioma_susceptibility_3|Medulloblastoma|Familial_cancer_of_breast|Uterine_corpus_cancer|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Wilms_tumor_1|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm": 1,
    "BRCA2-related_disorder|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Invasive_breast_carcinoma": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 5,
    "not_specified|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_provided|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|not_provided|Breast_and/or_ovarian_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Wilms_tumor_1|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_specified": 2,
    "not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast|not_specified": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|not_provided|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Fanconi_anemia_complementation_group_D1|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Medulloblastoma|Prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Breast_neoplasm|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast_neoplasm|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Infiltrating_duct_carcinoma_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|BRCA2-related_disorder|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 6,
    "Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Malignant_tumor_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Wilms_tumor_1|Glioma_susceptibility_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3": 5,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_neoplasm": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Ovarian_neoplasm|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Wilms_tumor_1|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Fanconi_anemia_complementation_group_D1|not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified": 2,
    "not_provided|BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 4,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|not_specified": 1,
    "BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Carcinoma_of_esophagus|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|BRCA2-related_cancer_predisposition": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 5,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 3,
    "Pancreatic_cancer|_susceptibility_to|_2": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 8,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Chordoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Familial_prostate_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|BRCA2-related_cancer_predisposition|Gastric_cancer|BRCA2-related_disorder|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Chordoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Inherited_ovarian_cancer_(without_breast_cancer)|BRCA2-related_cancer_predisposition": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 67,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_disorder|Familial_cancer_of_breast|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 6,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Prostate_cancer|Prostate_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_disorder|not_provided": 1,
    "BRCA2-related_disorder|Inherited_ovarian_cancer_(without_breast_cancer)|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1": 2,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Gastric_cancer|Rhabdomyosarcoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_prostate_cancer|Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hepatoblastoma|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|not_specified|BRCA2-related_cancer_predisposition": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Microprolactinoma|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2": 1,
    "Inherited_breast_cancer_and_ovarian_cancer": 5,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_and/or_ovarian_cancer|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Familial_colorectal_cancer_type_X|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_colorectal_cancer_type_X|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Familial_prostate_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_cancer|Infiltrating_duct_carcinoma_of_breast|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided": 2,
    "not_specified|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Prostate_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm": 1,
    "BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast|not_specified|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "not_provided|Fanconi_anemia_complementation_group_D1|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 3,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Gastric_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Prostate_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ovarian_cancer|Breast_neoplasm|Invasive_lobular_breast_carcinoma|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Familial_prostate_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Wilms_tumor_1|Medulloblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Genetic_non-acquired_premature_ovarian_failure|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Familial_prostate_cancer|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Diffuse_intrinsic_pontine_glioma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast": 1,
    "Familial_prostate_cancer|Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_pancreas|BRCA2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Familial_cancer_of_breast|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_specified|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Medulloblastoma|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Familial_prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided": 1,
    "not_provided|not_specified|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 3,
    "Chordoma|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 2,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Gastric_cancer": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_pancreatic_carcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "FLG-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Inherited_ovarian_cancer_(without_breast_cancer)|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|not_provided|BRCA2-related_disorder|not_specified|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_cancer_predisposition|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Breast_and/or_ovarian_cancer|not_provided|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Chordoma|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|BRCA2-related_cancer_predisposition|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast_neoplasm|Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Endometrial_carcinoma|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|not_specified": 1,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 9,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 4,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Intellectual_disability|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_esophagus": 1,
    "not_specified|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Glioma_susceptibility_3|Medulloblastoma|Wilms_tumor_1|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Metastatic_Prostate_Small_Cell_Carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|BRCA2-related_cancer_predisposition": 1,
    "not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 5,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|See_cases|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_pancreatic_carcinoma|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "not_provided|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Gastric_cancer|not_provided|Malignant_tumor_of_breast|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 2,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|BAP1-related_tumor_predisposition_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_carcinoma|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Malignant_tumor_of_breast|not_specified": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 5,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Gastric_cancer|Breast_carcinoma|not_provided|Breast_neoplasm|not_specified|Metastatic_Prostate_Small_Cell_Carcinoma|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Glioma_susceptibility_3|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Wilms_tumor_1": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Familial_pancreatic_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Esophageal_atresia/tracheoesophageal_fistula|Inherited_breast_cancer_and_ovarian_cancer|Breast_and/or_ovarian_cancer|not_provided|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 3,
    "Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_neoplasm": 1,
    "Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_specified|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Esophageal_atresia/tracheoesophageal_fistula|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_provided|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Familial_prostate_cancer|Wilms_tumor_1|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_provided|Ovarian_neoplasm|Endometrial_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "NICE_approved_PARP_inhibitor_treatment|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_neoplasm": 1,
    "Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_pancreatic_carcinoma": 4,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Ovarian_neoplasm": 1,
    "not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Infiltrating_duct_carcinoma_of_breast": 3,
    "Familial_cancer_of_breast|not_specified|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Glioma_susceptibility_3|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Inherited_breast_cancer_and_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "BRCA2-related_cancer_predisposition|Medulloblastoma|Familial_prostate_cancer|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|BRCA2-related_cancer_predisposition|not_specified|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|BRCA2-related_disorder|Malignant_tumor_of_breast|Malignant_tumor_of_pancreas|not_provided|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Wilms_tumor_1|Familial_prostate_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|BRCA2-related_cancer_predisposition|Inherited_breast_cancer_and_ovarian_cancer|Malignant_tumor_of_pancreas|BRCA2-related_disorder|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_pancreas|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition|Breast_neoplasm|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "not_specified|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Colorectal_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_carcinoma|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Wilms_tumor_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|not_provided|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Gastric_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Glioma_susceptibility_3|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Endometrial_carcinoma|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 139,
    "Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 3,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Breast_and/or_ovarian_cancer": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_colorectal_cancer_type_X": 1,
    "not_provided|not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "BRCA2-related_cancer_predisposition|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Prostate_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_cancer|_susceptibility_to|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Familial_pancreatic_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_specified|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_esophagus|Hereditary_nonpolyposis_colorectal_carcinoma": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Ovarian_neoplasm|not_provided|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|not_specified": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Inherited_ovarian_cancer_(without_breast_cancer)|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Malignant_tumor_of_breast|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Malignant_tumor_of_breast|Chordoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_D1|not_provided|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified|Breast_and/or_ovarian_cancer|BRCA2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Esophageal_atresia/tracheoesophageal_fistula|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Wilms_tumor_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|BRCA2-related_disorder": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_cancer|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Rhabdomyosarcoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_neoplasm|Malignant_tumor_of_breast|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Inherited_prostate_cancer": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Familial_prostate_cancer|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Endometrial_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer|BRCA2-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Breast_ductal_adenocarcinoma|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_D1|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Breast_neoplasm|not_specified|Medulloblastoma|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Gastric_cancer|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_pancreas|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition|BRCA2-related_disorder": 1,
    "Malignant_tumor_of_breast|Ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_neoplasm|Malignant_tumor_of_pancreas|Infiltrating_duct_carcinoma_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Chordoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Familial_prostate_cancer|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Esophageal_atresia/tracheoesophageal_fistula|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|BRCA2-related_cancer_predisposition|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Fanconi_anemia|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Medulloblastoma|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 2,
    "Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Carcinoma_of_colon|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast_neoplasm": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Malignant_tumor_of_breast|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|not_provided|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|not_provided|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Ovarian_neoplasm|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Uterine_corpus_cancer|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 58,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|not_provided": 1,
    "not_provided|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 2,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Medulloblastoma|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_disorder|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Gastric_cancer|BRCA2-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Infiltrating_duct_carcinoma_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome": 1,
    "Chordoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Wilms_tumor_1|Glioma_susceptibility_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Gastric_cancer|Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_cancer|_susceptibility_to|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Medulloblastoma|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_pancreas|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast_and/or_ovarian_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Genetic_non-acquired_premature_ovarian_failure|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|not_provided|not_specified": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_prostate_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Cancer_or_benign_tumor|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Familial_cancer_of_breast|Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Chordoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|BRCA2-related_disorder|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma": 1,
    "Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_neoplasm": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|BRCA2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hearing_impairment|Cerebral_palsy|Neurodevelopmental_delay|Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Malignant_tumor_of_breast|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Carcinoma_of_colon": 1,
    "Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Familial_cancer_of_breast|Familial_colorectal_cancer_type_X|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 2,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_provided|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified": 1,
    "not_provided|Ovarian_cancer|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Familial_prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|not_specified": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Familial_prostate_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|not_specified|BRCA2-related_disorder": 1,
    "BRCA2-related_cancer_predisposition|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Prostate_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "not_specified|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Glioma_susceptibility_3|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Familial_pancreatic_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder": 1,
    "BRCA2-related_disorder|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ovarian_cancer|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "not_provided|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Wilms_tumor_1|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer": 1,
    "NICE_approved_PARP_inhibitor_treatment|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_prostate_cancer|Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_prostate_cancer|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Neuroblastoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|Familial_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Breast_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|BRCA2-related_disorder|not_specified": 1,
    "Breast_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Medulloblastoma|Prostate_cancer": 1,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Wilms_tumor_1|Glioma_susceptibility_3": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_specified": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Breast_and/or_ovarian_cancer|Malignant_lymphoma|_large_B-cell|_diffuse|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma|See_cases|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_provided|not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Prostate_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Wilms_tumor_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Gastric_cancer|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Esophageal_atresia/tracheoesophageal_fistula|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ateleiotic_dwarfism|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder|BRCA2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Cancer_or_benign_tumor|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Medulloblastoma|Wilms_tumor_1|Familial_prostate_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_pancreas": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA2-related_disorder|Medulloblastoma|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Polydactyly|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|BRCA2-related_cancer_predisposition|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|not_specified|BRCA2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_prostate_cancer|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Ovarian_neoplasm|not_provided|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Wilms_tumor_1|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|NICE_approved_PARP_inhibitor_treatment|Inherited_breast_cancer_and_ovarian_cancer|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|not_specified|Familial_cancer_of_breast|BRCA2-related_cancer_predisposition|Malignant_tumor_of_breast|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "BRCA2-related_cancer_predisposition|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "NICE_approved_PARP_inhibitor_treatment|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|NICE_approved_PARP_inhibitor_treatment|BRCA2-related_cancer_predisposition|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|Breast_neoplasm|Gastric_cancer|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Prostate_cancer|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|BRCA2-related_disorder": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|BRCA2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Medulloblastoma|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Wilms_tumor_1|Glioma_susceptibility_3|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_disorder|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Wilms_tumor_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_disorder": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast": 1,
    "not_provided|Atypical_teratoid_rhabdoid_tumor|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Prostate_cancer|Medulloblastoma|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "BRCA2-related_cancer_predisposition|Medulloblastoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Endometrial_cancer": 1,
    "not_specified|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_neoplasm|Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Fanconi_anemia_complementation_group_D1|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_prostate_cancer": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Inherited_ovarian_cancer_(without_breast_cancer)|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|BRCA2-related_cancer_predisposition|not_provided|BRCA2-related_disorder": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|not_specified|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Ovarian_neoplasm": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|not_provided": 1,
    "BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Genetic_non-acquired_premature_ovarian_failure|BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA2-related_disorder|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Medulloblastoma|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Glioma_susceptibility_3|Pancreatic_cancer|_susceptibility_to|_2|Wilms_tumor_1|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Rhabdomyosarcoma|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Fanconi_anemia_complementation_group_D1|Wilms_tumor_1|Medulloblastoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Inherited_breast_cancer_and_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "BRCA2-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Malignant_tumor_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Familial_cancer_of_breast|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA2-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_D1|Medulloblastoma|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_prostate_cancer|Wilms_tumor_1|Polyposis_syndrome|_hereditary_mixed|_1": 1,
    "BRCA2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition|not_specified|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Wilms_tumor_1|Fanconi_anemia_complementation_group_D1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Familial_prostate_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "NICE_approved_PARP_inhibitor_treatment": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer|not_specified": 1,
    "Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 2,
    "not_provided|Fanconi_anemia_complementation_group_D1|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRCA2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|Glioma_susceptibility_3|Medulloblastoma|Wilms_tumor_1|Prostate_cancer|Pancreatic_cancer|_susceptibility_to|_2|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|BRCA2-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Familial_pancreatic_carcinoma|Familial_cancer_of_breast|Wilms_tumor_1|Pancreatic_cancer|_susceptibility_to|_2|Glioma_susceptibility_3|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Medulloblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_pancreas": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Malignant_tumor_of_pancreas|BRCA2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA2-related_disorder|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|BRCA2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|BRCA2-related_cancer_predisposition": 1,
    "BRCA2-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_D1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA2-related_cancer_predisposition|Breast_neoplasm|Glioma_susceptibility_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Pancreatic_cancer|_susceptibility_to|_2|Prostate_cancer|Fanconi_anemia_complementation_group_D1|Familial_cancer_of_breast|Wilms_tumor_1|Medulloblastoma|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "BRCA2-related_disorder|not_provided|BRCA2-related_cancer_predisposition|not_specified": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 1,
    "Fanconi_anemia_complementation_group_D1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 9,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1|not_provided": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_D1": 2,
    "Fanconi_anemia_complementation_group_D1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_D1|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "PDS5B-related_developmental_disorder": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_provided": 36,
    "not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3": 25,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3": 57,
    "not_provided|not_specified|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3": 2,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_specified|not_provided": 2,
    "KL-related_disorder|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3": 3,
    "not_specified|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_provided": 2,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_specified": 1,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_provided|KL-related_disorder": 3,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_1": 1,
    "not_provided|KL-related_disorder": 1,
    "not_specified|not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3": 2,
    "not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|KL-related_disorder": 1,
    "KL-related_disorder|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_provided": 2,
    "not_provided|KL-related_disorder|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3": 2,
    "Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_provided|not_specified": 3,
    "not_provided|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_specified": 2,
    "Amenorrhea|Tumoral_calcinosis|_hyperphosphatemic|_familial|_3|not_specified": 1,
    "KL-related_disorder": 1,
    "Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy": 109,
    "NBEA-related_disorder": 41,
    "NBEA-related_disorder|not_provided": 13,
    "not_specified|NBEA-related_disorder|not_provided": 2,
    "not_provided|NBEA-related_disorder": 9,
    "Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|not_provided": 8,
    "NBEA-related_intellectual_disability": 2,
    "NBEA-related_disorder|Inborn_genetic_diseases": 1,
    "NBEA-related_complex_neurodevelopmental_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|NBEA-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy": 1,
    "Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy": 9,
    "not_provided|Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy": 2,
    "NBEA-related_disorder|Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NBEA-related_disorder": 3,
    "not_provided|NBEA-related_disorder|Inborn_genetic_diseases": 1,
    "Epilepsy|Neurodevelopmental_delay": 3,
    "Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|See_cases|not_specified": 1,
    "Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|NBEA-related_developmental_delay_and_generalized_epilepsy": 1,
    "Intellectual_disability_and_seizures": 1,
    "not_provided|Inborn_genetic_diseases|NBEA-related_disorder": 1,
    "NBEA-related_disorder|not_provided|Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|Inborn_genetic_diseases|not_specified": 1,
    "Cerebellar|_ocular|_craniofacial|_and_genital_syndrome": 5,
    "MAB21L1-related_disorder|not_provided": 1,
    "MAB21L1-related_disorder": 1,
    "Hypoplasia_of_scrotum": 1,
    "Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy|Cerebellar|_ocular|_craniofacial|_and_genital_syndrome": 1,
    "not_specified|Neurodevelopmental_disorder_with_or_without_early-onset_generalized_epilepsy": 1,
    "typical_paroxysmal_kinesigenic_dyskinesia": 1,
    "CCDC169-SOHLH2-related_disorder": 5,
    "SOHLH2-related_disorder": 7,
    "Troyer_syndrome": 64,
    "not_provided|Troyer_syndrome": 11,
    "Troyer_syndrome|not_provided": 12,
    "Inborn_genetic_diseases|Troyer_syndrome|not_provided": 2,
    "not_provided|SPART-related_disorder": 2,
    "not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 3,
    "SPART-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Troyer_syndrome": 3,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Troyer_syndrome": 1,
    "SPART-related_disorder": 3,
    "Troyer_syndrome|Global_developmental_delay|Microcephaly|Cerebellar_ataxia|Strabismus|Dysarthria|Failure_to_thrive": 1,
    "not_provided|Neurodevelopmental_delay|Troyer_syndrome": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|not_provided": 1,
    "SPART-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Troyer_syndrome": 1,
    "not_provided|Troyer_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "SPART-related_disorder|not_provided|Troyer_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 3,
    "Troyer_syndrome|Inborn_genetic_diseases": 1,
    "Troyer_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Troyer_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Troyer_syndrome|Neurodevelopmental_delay": 1,
    "SPART-related_disorder|not_specified|not_provided|Troyer_syndrome|Hereditary_spastic_paraplegia": 1,
    "SPART-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Troyer_syndrome": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Troyer_syndrome": 1,
    "not_specified|Troyer_syndrome": 1,
    "MHC_class_II_deficiency|RFXAP-related_disorder|not_provided": 1,
    "MHC_class_II_deficiency_4": 9,
    "MHC_class_II_deficiency_4|not_provided|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency|MHC_class_II_deficiency_4": 1,
    "MHC_class_II_deficiency_1|MHC_class_II_deficiency|MHC_class_II_deficiency_4": 1,
    "RFXAP-related_disorder|MHC_class_II_deficiency": 1,
    "Pulmonary_hypertension|_primary|_2": 158,
    "SMAD9-related_disorder": 2,
    "not_provided|Pulmonary_hypertension|_primary|_2": 4,
    "Pulmonary_hypertension|_primary|_2|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Pulmonary_hypertension|_primary|_2": 1,
    "Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_hypertension|_primary|_2": 1,
    "Pulmonary_hypertension|_primary|_2|Pulmonary_hypertension|_primary|_1": 1,
    "not_provided|SMAD9-related_disorder|Pulmonary_hypertension|_primary|_2": 1,
    "Pulmonary_hypertension|_primary|_2|not_specified": 1,
    "Pulmonary_hypertension|_primary|_2|not_provided|SMAD9-related_disorder": 1,
    "not_specified|Pulmonary_hypertension|_primary|_2": 2,
    "Inborn_genetic_diseases|Pulmonary_hypertension|_primary|_2": 3,
    "Pulmonary_hypertension|_primary|_2|Inborn_genetic_diseases": 9,
    "SMAD9-related_disorder|Pulmonary_hypertension|_primary|_2|not_provided": 1,
    "Pulmonary_hypertension|_primary|_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Pulmonary_hypertension|_primary|_2": 1,
    "Inborn_genetic_diseases|SMAD9-related_disorder": 1,
    "SMAD9-related_disorder|Pulmonary_hypertension|_primary|_2": 1,
    "Pulmonary_hypertension|_primary|_2|SMAD9-related_disorder": 1,
    "not_provided|not_specified|Pulmonary_hypertension|_primary|_2": 1,
    "not_specified|not_provided|SMAD9-related_disorder|Pulmonary_hypertension|_primary|_2": 1,
    "not_provided|Pulmonary_hypertension|_primary|_2|not_specified": 1,
    "Polycystic_kidney_disease_7": 13,
    "ALG5-related_disorder": 9,
    "Polycystic_kidney_disease_7|not_specified": 1,
    "not_specified|ALG5-related_disorder": 2,
    "ALG5-related_disorder|not_specified": 1,
    "Pontocerebellar_hypoplasia|_type_1C": 7,
    "Pontocerebellar_hypoplasia|_type_1C|not_specified|not_provided": 2,
    "EXOSC8-related_disorder": 2,
    "Pontocerebellar_hypoplasia|_type_1C|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia|_type_1C": 3,
    "not_provided|not_specified|Pontocerebellar_hypoplasia|_type_1C": 1,
    "not_provided|EXOSC8-related_disorder": 1,
    "not_provided|EXOSC8-related_disorder|not_specified": 1,
    "EXOSC8-related_disorder|not_provided": 1,
    "Leukodystrophy|_hypomyelinating|_14|not_provided": 3,
    "Leukodystrophy|_hypomyelinating|_14": 1,
    "UFM1-related_disorder": 2,
    "not_provided|Leukodystrophy|_hypomyelinating|_14": 2,
    "not_provided|UFM1-related_disorder": 1,
    "Fraser_syndrome_2|not_provided": 36,
    "Fraser_syndrome_2": 155,
    "not_provided|Fraser_syndrome_2": 39,
    "Fraser_syndrome_2|Isolated_cryptophthalmia": 273,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|not_provided": 32,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided|not_specified": 3,
    "FREM2-related_disorder|not_provided": 18,
    "FREM2-related_disorder": 28,
    "not_provided|Isolated_cryptophthalmia|Fraser_syndrome_2|FREM2-related_disorder": 1,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|FREM2-related_disorder|not_provided": 2,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|Inborn_genetic_diseases": 21,
    "FREM2-related_disorder|Fraser_syndrome_2|not_provided": 4,
    "Isolated_cryptophthalmia|Fraser_syndrome_2": 6,
    "not_provided|Fraser_syndrome_2|FREM2-related_disorder|not_specified": 2,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Isolated_cryptophthalmia|Fraser_syndrome_2": 10,
    "Fraser_syndrome_2|not_specified|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|FREM2-related_disorder|Fraser_syndrome_2": 1,
    "Inborn_genetic_diseases|Fraser_syndrome_2|Isolated_cryptophthalmia": 22,
    "Inborn_genetic_diseases|Isolated_cryptophthalmia|Fraser_syndrome_2|not_provided": 2,
    "not_provided|Fraser_syndrome_2|Isolated_cryptophthalmia|FREM2-related_disorder": 3,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|Inborn_genetic_diseases": 23,
    "not_provided|FREM2-related_disorder|Fraser_syndrome_2|Isolated_cryptophthalmia": 1,
    "not_specified|Isolated_cryptophthalmia|not_provided|Fraser_syndrome_2|Fraser_syndrome_1": 1,
    "Fraser_syndrome_2|FREM2-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Fraser_syndrome_2": 4,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Isolated_cryptophthalmia|Fraser_syndrome_2": 1,
    "FREM2-related_disorder|not_provided|Isolated_cryptophthalmia|Fraser_syndrome_2": 2,
    "not_provided|Isolated_cryptophthalmia|Fraser_syndrome_2": 20,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided": 15,
    "Fraser_syndrome_2|not_provided|FREM2-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Fraser_syndrome_2|Isolated_cryptophthalmia": 7,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Isolated_cryptophthalmia|Fraser_syndrome_2|not_provided|FREM2-related_disorder": 1,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|Inborn_genetic_diseases|not_provided": 6,
    "not_provided|Fraser_syndrome_2|Isolated_cryptophthalmia|Inborn_genetic_diseases": 4,
    "not_provided|Fraser_syndrome_2|Isolated_cryptophthalmia": 13,
    "not_provided|not_specified|Fraser_syndrome_2|Inborn_genetic_diseases|FREM2-related_disorder": 1,
    "not_provided|Microcephaly|Fraser_syndrome_2|Isolated_cryptophthalmia": 2,
    "Fraser_syndrome_2|Inborn_genetic_diseases|Isolated_cryptophthalmia|not_provided": 3,
    "not_provided|FREM2-related_disorder": 13,
    "Inborn_genetic_diseases|not_provided|Fraser_syndrome_2|Isolated_cryptophthalmia": 6,
    "FREM2-related_disorder|Fraser_syndrome_2|not_specified|not_provided": 1,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|FREM2-related_disorder": 2,
    "Fraser_syndrome_2|FREM2-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Fraser_syndrome_2|not_provided": 1,
    "not_specified|not_provided|Fraser_syndrome_2": 2,
    "FREM2-related_disorder|Isolated_cryptophthalmia|Fraser_syndrome_2": 3,
    "Fraser_syndrome_1|not_provided|Fraser_syndrome_2|not_specified": 1,
    "not_specified|Fraser_syndrome_2|FREM2-related_disorder|not_provided": 2,
    "Fraser_syndrome_2|not_specified": 1,
    "not_provided|Isolated_cryptophthalmia|Fraser_syndrome_2|Inborn_genetic_diseases": 2,
    "FREM2-related_disorder|Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided": 1,
    "not_provided|Fraser_syndrome_2|FREM2-related_disorder": 4,
    "FREM2-related_disorder|not_specified|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Isolated_cryptophthalmia|Fraser_syndrome_2": 6,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|not_provided|Fraser_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|FREM2-related_disorder|Isolated_cryptophthalmia|Fraser_syndrome_2": 1,
    "not_specified|Fraser_syndrome_1|FREM2-related_disorder|not_provided": 1,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "Fraser_syndrome_2|FREM2-related_disorder|Isolated_cryptophthalmia|not_provided": 1,
    "Fraser_syndrome_1|Fraser_syndrome_2|not_specified|not_provided|Isolated_cryptophthalmia": 1,
    "Fraser_syndrome_2|not_provided|FREM2-related_disorder": 8,
    "Isolated_cryptophthalmia": 1,
    "Fraser_syndrome_2|not_provided|FREM2-related_disorder|Isolated_cryptophthalmia": 2,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Congenital_diaphragmatic_hernia|FREM2-related_disorder|not_specified": 1,
    "not_provided|FREM2-related_disorder|Fraser_syndrome_2": 5,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided|FREM2-related_disorder": 1,
    "not_provided|FREM2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Isolated_cryptophthalmia|Fraser_syndrome_2": 1,
    "not_specified|not_provided|Isolated_cryptophthalmia|Fraser_syndrome_2": 1,
    "Fraser_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Fraser_syndrome_2|not_specified|FREM2-related_disorder": 1,
    "not_provided|Fraser_syndrome_2|Inborn_genetic_diseases": 1,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Fraser_syndrome_2": 3,
    "Congenital_diaphragmatic_hernia|not_provided": 1,
    "Fraser_syndrome_2|not_provided|not_specified": 2,
    "not_provided|Fraser_syndrome_2|Isolated_cryptophthalmia|not_specified": 2,
    "Fraser_syndrome_2|not_provided|Isolated_cryptophthalmia": 2,
    "not_provided|Isolated_cryptophthalmia": 1,
    "Fraser_syndrome_1|Fraser_syndrome_2": 1,
    "Fraser_syndrome_2|not_provided|Isolated_cryptophthalmia|FREM2-related_disorder": 1,
    "not_provided|Cryptophthalmia|Ambiguous_genitalia|Toe_syndactyly|Cryptotia|Abnormality_of_the_anus|Unilateral_renal_agenesis|Renal_hypoplasia/aplasia|Finger_syndactyly|Fraser_syndrome_1": 1,
    "not_provided|not_specified|Fraser_syndrome_2": 1,
    "Inborn_genetic_diseases|Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided": 2,
    "Isolated_cryptophthalmia|not_specified|not_provided|Fraser_syndrome_2|Fraser_syndrome_1": 1,
    "not_provided|Fraser_syndrome_2|not_specified": 1,
    "not_specified|Fraser_syndrome_2|not_provided|Isolated_cryptophthalmia|FREM2-related_disorder": 1,
    "Isolated_cryptophthalmia|not_provided|not_specified|Fraser_syndrome_2": 1,
    "FREM2-related_disorder|not_provided|Fraser_syndrome_2": 1,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|not_specified|not_provided": 1,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|Fraser_syndrome_1|not_provided": 1,
    "not_specified|Fraser_syndrome_2|Congenital_anomaly_of_kidney_and_urinary_tract|Isolated_cryptophthalmia|not_provided": 1,
    "not_specified|Fraser_syndrome_2|not_provided": 1,
    "FREM2-related_disorder|Fraser_syndrome_2|Epidermolysis_bullosa_simplex_with_nail_dystrophy|not_provided": 1,
    "not_specified|Isolated_cryptophthalmia|Fraser_syndrome_2|not_provided": 1,
    "Isolated_cryptophthalmia|not_provided": 1,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|not_provided|Fraser_syndrome_1": 1,
    "Fraser_syndrome_2|not_specified|Isolated_cryptophthalmia|not_provided": 1,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|FREM2-related_disorder": 1,
    "Fraser_syndrome_2|FREM2-related_disorder|Isolated_cryptophthalmia|not_specified|not_provided|Fraser_syndrome_1": 1,
    "Fraser_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Isolated_cryptophthalmia|Fraser_syndrome_2|not_specified|not_provided": 1,
    "Fraser_syndrome_2|Isolated_cryptophthalmia|FREM2-related_disorder|not_specified|not_provided": 1,
    "FREM2-related_disorder|Fraser_syndrome_2|Isolated_cryptophthalmia|Inborn_genetic_diseases": 1,
    "not_provided|FREM2-related_disorder|not_specified": 1,
    "PROSER1-related_disorder": 1,
    "LHFPL6-related_disorder": 2,
    "not_provided|COG6-congenital_disorder_of_glycosylation": 7,
    "COG6-congenital_disorder_of_glycosylation": 54,
    "Congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_specified|COG6-related_disorder|Congenital_disorder_of_glycosylation": 1,
    "not_specified|COG6-related_disorder|COG6-congenital_disorder_of_glycosylation": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 60,
    "not_provided|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|not_specified": 1,
    "COG6-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation": 2,
    "not_provided|Inborn_genetic_diseases|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-related_disorder": 1,
    "not_specified|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 1,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation": 18,
    "not_specified|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|not_provided": 1,
    "Inborn_genetic_diseases|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 7,
    "not_provided|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|not_specified": 2,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|not_provided": 4,
    "COG6-related_disorder": 14,
    "COG6-congenital_disorder_of_glycosylation|not_provided|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_provided": 2,
    "COG6-related_disorder|not_provided|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 1,
    "COG6-related_disorder|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 3,
    "COG6-congenital_disorder_of_glycosylation|COG6-related_disorder": 1,
    "COG6-congenital_disorder_of_glycosylation|not_provided": 2,
    "Inborn_genetic_diseases|COG6-congenital_disorder_of_glycosylation": 3,
    "Inborn_genetic_diseases|not_provided|COG6-congenital_disorder_of_glycosylation": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_specified|not_provided|Congenital_disorder_of_glycosylation": 1,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_provided|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 3,
    "not_provided|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation": 1,
    "not_provided|not_specified|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation": 1,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|not_specified|not_provided": 2,
    "not_provided|not_specified|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|Inborn_genetic_diseases": 3,
    "not_specified|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|COG6-related_disorder": 1,
    "COG6-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|COG6-related_disorder": 1,
    "COG6-related_disorder|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_provided|COG6-congenital_disorder_of_glycosylation|Hypohidrosis|Intellectual_disability": 1,
    "not_specified|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation": 2,
    "not_provided|not_specified|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|COG6-related_disorder": 1,
    "Inborn_genetic_diseases|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_provided": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-related_disorder": 2,
    "not_specified|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_specified|Congenital_disorder_of_glycosylation": 1,
    "COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_provided|not_specified": 1,
    "not_provided|COG6-related_disorder": 1,
    "Inborn_genetic_diseases|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_specified": 1,
    "not_provided|COG6-congenital_disorder_of_glycosylation|Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|not_specified": 1,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "Hypohidrosis-enamel_hypoplasia-palmoplantar_keratoderma-intellectual_disability_syndrome|COG6-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "FOXO1-related_disorder|not_provided": 1,
    "FOXO1-related_disorder": 1,
    "not_provided|FOXO1-related_disorder": 1,
    "not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 16,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|not_specified": 5,
    "not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|Cardiac_arrhythmia|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|Inborn_genetic_diseases": 8,
    "not_specified|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|SLC25A15-related_disorder": 1,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|not_provided": 4,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 6,
    "not_provided|Inborn_genetic_diseases|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 1,
    "SLC25A15-related_disorder|not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|Intellectual_disability": 1,
    "not_specified|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 5,
    "SLC25A15-related_disorder|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 1,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|Abnormal_facial_shape|Intellectual_disability": 1,
    "SLC25A15-related_disorder|not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 1,
    "not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|SLC25A15-related_disorder|Inborn_genetic_diseases": 1,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "SLC25A15-related_disorder": 1,
    "Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome|SLC25A15-related_disorder": 1,
    "not_specified|not_provided|Hyperornithinemia-hyperammonemia-homocitrullinuria_syndrome": 1,
    "Neurodevelopmental_disorder|Neurodevelopmental_disorder_with_hypotonia|_feeding_difficulties|_facial_dysmorphism|_and_brain_abnormalities": 1,
    "Nonsyndromic_cleft_lip_palate|not_specified": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_23": 31,
    "not_provided|Retinitis_pigmentosa_97|Nonsyndromic_cleft_lip_palate": 1,
    "Developmental_delay|not_provided": 1,
    "AKAP11-related_disorder|not_specified": 1,
    "not_specified|AKAP11-related_disorder": 1,
    "AKAP11-related_disorder": 2,
    "Autosomal_recessive_osteopetrosis_2": 40,
    "not_provided|Autosomal_recessive_osteopetrosis_2": 4,
    "TNFSF11-related_disorder|not_provided|Autosomal_recessive_osteopetrosis_2": 1,
    "not_specified|Autosomal_recessive_osteopetrosis_2|Increased_bone_mineral_density|not_provided": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_2|TNFSF11-related_disorder": 1,
    "Autosomal_recessive_osteopetrosis_2|not_provided": 9,
    "TNFSF11-related_disorder|not_provided": 3,
    "not_specified|Increased_bone_mineral_density|Autosomal_recessive_osteopetrosis_2|not_provided": 1,
    "not_specified|Autosomal_recessive_osteopetrosis_2|not_provided": 2,
    "Autosomal_recessive_osteopetrosis_2|not_provided|not_specified": 1,
    "Autosomal_recessive_osteopetrosis_2|TNFSF11-related_disorder|not_provided": 1,
    "Increased_bone_mineral_density|Autosomal_recessive_osteopetrosis_2|not_provided": 3,
    "TNFSF11-related_disorder": 2,
    "Autosomal_recessive_osteopetrosis_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_osteopetrosis_2": 1,
    "TNFSF11-related_disorder|Autosomal_recessive_osteopetrosis_2|not_provided": 1,
    "Autosomal_recessive_osteopetrosis_2|Inborn_genetic_diseases|not_provided": 1,
    "Juvenile_arthritis_due_to_defect_in_LACC1": 7,
    "Leprosy|_susceptibility_to|_1|not_provided|Juvenile_arthritis_due_to_defect_in_LACC1|not_specified": 1,
    "Juvenile_arthritis_due_to_defect_in_LACC1|not_provided": 1,
    "not_provided|Juvenile_arthritis_due_to_defect_in_LACC1": 1,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_10": 4,
    "Congenital_disorder_of_glycosylation|_type_IIbb": 3,
    "CPB2-related_disorder": 9,
    "HTR2A-related_disorder|not_provided": 1,
    "Major_depressive_disorder|_response_to_citalopram_therapy_in|not_specified": 1,
    "not_specified|Schizophrenia|_susceptibility_to": 1,
    "Obsessive-compulsive_disorder|_susceptibility_to|Cocaine-Related_Disorders|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 233,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 16,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_specified": 2,
    "not_specified|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided": 2,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided": 11,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|SUCLA2-related_disorder": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 5,
    "SUCLA2-related_disorder|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 4,
    "not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 3,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided": 1,
    "SUCLA2-related_disorder": 8,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided|not_specified": 2,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided|SUCLA2-related_disorder|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|SUCLA2-related_disorder|not_provided|not_specified": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 7,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 5,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|Inborn_genetic_diseases": 5,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 3,
    "SUCLA2-related_disorder|not_provided|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|SUCLA2-related_disorder": 2,
    "Inborn_genetic_diseases|SUCLA2-related_disorder|Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_provided|Global_developmental_delay": 1,
    "Mitochondrial_DNA_depletion_syndrome|_encephalomyopathic_form_with_methylmalonic_aciduria|not_specified|not_provided": 1,
    "not_provided|SUCLA2-related_disorder": 1,
    "NUDT15-related_disorder|Thiopurines|_poor_metabolism_of|_2": 2,
    "not_provided|NUDT15-related_disorder": 1,
    "NUDT15-related_disorder": 2,
    "azathioprine_response_-_Toxicity|mercaptopurine_response_-_Dosage|NUDT15-related_disorder|Thiopurines|_poor_metabolism_of|_2": 1,
    "Thiopurines|_poor_metabolism_of|_2": 1,
    "ADan_amyloidosis": 2,
    "not_provided|ITM2B-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|ADan_amyloidosis|ABri_amyloidosis|Retinal_dystrophy_with_inner_retinal_dysfunction_and_ganglion_cell_anomalies": 1,
    "not_provided|ITM2B-related_disorder": 2,
    "Inborn_genetic_diseases|ITM2B-related_disorder": 1,
    "ITM2B-related_disorder|not_provided": 1,
    "Retinal_dystrophy_with_inner_retinal_dysfunction_and_ganglion_cell_anomalies": 1,
    "ABri_amyloidosis": 2,
    "Retinoblastoma|RB1-related_disorder|not_provided": 1,
    "Retinoblastoma": 1984,
    "RB1-related_disorder|Retinoblastoma": 6,
    "Hereditary_cancer-predisposing_syndrome|RB1-related_disorder|Retinoblastoma|not_provided": 1,
    "not_provided|Retinoblastoma": 29,
    "Retinoblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 14,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 519,
    "RB1-related_disorder": 12,
    "Retinoblastoma|not_provided": 25,
    "Malignant_tumor_of_urinary_bladder|not_provided|Retinoblastoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 413,
    "Retinoblastoma|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 5,
    "Retinoblastoma|Malignant_tumor_of_urinary_bladder": 8,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|not_provided": 16,
    "not_specified|Retinoblastoma": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma": 28,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 8,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Retinoblastoma": 12,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Bone_osteosarcoma|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma": 2,
    "not_provided|RB1-related_disorder|not_specified|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Retinoblastoma": 8,
    "RB1-related_disorder|not_specified|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Retinal_dystrophy|Retinoblastoma": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 21,
    "not_provided|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 14,
    "not_provided|Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Retinoblastoma|RB1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|RB1-related_disorder": 3,
    "Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 6,
    "Malignant_tumor_of_urinary_bladder|Retinoblastoma": 7,
    "Malignant_tumor_of_urinary_bladder|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder": 3,
    "Retinoblastoma|not_specified": 9,
    "Retinoblastoma|Bone_osteosarcoma|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Bone_osteosarcoma|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Retinoblastoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Retinoblastoma|Bone_osteosarcoma|Small_cell_lung_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Small_cell_lung_carcinoma|Malignant_tumor_of_urinary_bladder|Retinoblastoma|Bone_osteosarcoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|Ovarian_neoplasm": 1,
    "not_provided|Retinoblastoma|RB1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "RB1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Retinoblastoma": 1,
    "not_provided|Retinoblastoma|not_specified": 1,
    "not_specified|Retinoblastoma|not_provided": 1,
    "RB1-related_disorder|Hereditary_cancer-predisposing_syndrome|Retinoblastoma|Small_cell_lung_carcinoma|Malignant_tumor_of_urinary_bladder|Bone_osteosarcoma|not_specified|not_provided": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder": 10,
    "Small_cell_lung_carcinoma|Retinoblastoma|Bone_osteosarcoma|Malignant_tumor_of_urinary_bladder": 4,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|RB1-related_disorder|not_provided": 2,
    "Retinoblastoma|not_provided|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 1,
    "Retinoblastoma|Malignant_tumor_of_urinary_bladder|Bone_osteosarcoma|Small_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Retinoblastoma|not_specified|not_provided": 1,
    "Retinoblastoma|RB1-related_disorder": 1,
    "RB1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Malignant_tumor_of_urinary_bladder|Retinoblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma|Lynch_syndrome_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Small_cell_lung_carcinoma|Malignant_tumor_of_urinary_bladder|Retinoblastoma|Bone_osteosarcoma|not_provided": 1,
    "not_specified|RB1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma": 1,
    "Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Bone_osteosarcoma|Retinoblastoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Bone_osteosarcoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|Malignant_tumor_of_urinary_bladder": 8,
    "RB1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Bone_osteosarcoma|Small_cell_lung_carcinoma": 3,
    "not_provided|Retinoblastoma|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 2,
    "Retinoblastoma|Hereditary_retinoblastoma": 1,
    "not_specified|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Bone_osteosarcoma|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Retinoblastoma": 4,
    "Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Retinoblastoma|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Bone_osteosarcoma|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Retinoblastoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder|Retinoblastoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|not_provided|Malignant_tumor_of_urinary_bladder": 1,
    "Optic_atrophy|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Retinoblastoma": 2,
    "Retinoblastoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Retinoblastoma": 2,
    "Retinoblastoma|RB1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma|Malignant_tumor_of_urinary_bladder": 2,
    "Bone_osteosarcoma|Small_cell_lung_carcinoma|Retinoblastoma|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Retinoblastoma": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Bone_osteosarcoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder|Retinoblastoma|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Retinoblastoma|not_provided": 1,
    "Malignant_tumor_of_urinary_bladder|Retinoblastoma|RB1-related_disorder": 1,
    "Retinoblastoma|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "RB1-related_disorder|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|Ovarian_cancer|not_specified|not_provided": 1,
    "Hereditary_retinoblastoma": 1,
    "not_provided|RB1-related_disorder|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "Trilateral_retinoblastoma|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Hypotrichosis_8": 18,
    "LPAR6-related_disorder": 1,
    "LPAR6-related_disorder|not_provided": 1,
    "Wooly_hair|_autosomal_recessive_1|_with_or_without_hypotrichosis|Hypotrichosis_8": 1,
    "Wooly_hair|_autosomal_recessive_1|_with_or_without_hypotrichosis": 1,
    "Wooly_hair|_autosomal_recessive_1|_with_or_without_hypotrichosis|Wooly_hair|_autosomal_recessive_3|Hypotrichosis_8|not_provided": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "not_provided|not_specified|Retinoblastoma|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|RB1-related_disorder|Retinoblastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Retinoblastoma|not_specified": 2,
    "RB1-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Bone_osteosarcoma|Small_cell_lung_carcinoma|Retinoblastoma|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "Retinoblastoma|Hereditary_cancer-predisposing_syndrome|RB1-related_disorder": 1,
    "Hereditary_retinoblastoma|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Retinoblastoma|RB1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "RB1-related_disorder|Retinoblastoma|not_provided": 1,
    "RB1-related_disorder|not_provided|Retinoblastoma": 1,
    "RB1-related_disorder|not_specified|Retinoblastoma": 1,
    "Small_cell_lung_carcinoma|Retinoblastoma": 1,
    "Retinoblastoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Retinal_dystrophy|not_specified|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Medulloblastoma|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Retinoblastoma|Bone_osteosarcoma|not_provided": 1,
    "not_provided|Retinoblastoma|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Retinoblastoma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|RB1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Retinoblastoma|RB1-related_disorder": 1,
    "RB1-related_disorder|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Hereditary_retinoblastoma|Retinoblastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_urinary_bladder|Retinoblastoma": 1,
    "B_lymphoblastic_leukemia_lymphoma_with_t(12%3B21)(p13%3Bq22)%3B_TEL-AML1_(ETV6-RUNX1)|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "B_Lymphoblastic_Leukemia/Lymphoma|_Not_Otherwise_Specified|Retinoblastoma|Hereditary_cancer-predisposing_syndrome|RB1-related_disorder|not_specified|not_provided": 1,
    "RB1-related_disorder|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|Retinoblastoma": 1,
    "Retinoblastoma|not_provided|not_specified": 1,
    "Retinoblastoma|Malignant_tumor_of_urinary_bladder|Small_cell_lung_carcinoma|Bone_osteosarcoma": 1,
    "FNDC3A-related_disorder": 7,
    "FNDC3A-related_disorder|not_provided": 1,
    "PHF11-related_disorder": 4,
    "not_provided|RCBTB1-related_retinopathy": 6,
    "RCBTB1-related_disorder": 2,
    "RCBTB1-related_disorder|not_provided": 3,
    "not_provided|RCBTB1-related_disorder": 2,
    "not_provided|Exudative_retinopathy|Familial_exudative_vitreoretinopathy": 1,
    "RCBTB1-related_retinopathy|Retinitis_pigmentosa": 1,
    "not_provided|RCBTB1-related_disorder|not_specified": 1,
    "RCBTB1-related_disorder|Retinitis_pigmentosa|RETINAL_DYSTROPHY_WITH_EXTRAOCULAR_ANOMALIES|RCBTB1-related_retinopathy|not_provided": 1,
    "Retinitis_pigmentosa|RETINAL_DYSTROPHY_WITH_EXTRAOCULAR_ANOMALIES|not_provided": 1,
    "Retinitis_pigmentosa|RCBTB1-related_retinopathy": 1,
    "Exudative_retinopathy|RCBTB1-related_retinopathy|not_provided": 1,
    "RCBTB1-related_retinopathy": 1,
    "RCBTB1-related_retinopathy|not_provided": 1,
    "Spastic_paraplegia_88|_autosomal_dominant": 8,
    "not_provided|Spastic_paraplegia_88|_autosomal_dominant": 1,
    "KPNA3-related_condition": 1,
    "Aicardi-Goutieres_syndrome_2": 396,
    "not_provided|Aicardi-Goutieres_syndrome_2": 12,
    "Aicardi-Goutieres_syndrome_2|not_provided": 7,
    "Aicardi-Goutieres_syndrome_2|RNASEH2B-related_disorder": 2,
    "Aicardi-Goutieres_syndrome_2|Inborn_genetic_diseases": 18,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_2": 4,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_2|not_specified|not_provided": 1,
    "not_specified|Aicardi-Goutieres_syndrome_2": 2,
    "not_provided|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_2|RNASEH2B-related_disorder": 1,
    "Global_developmental_delay|Aicardi-Goutieres_syndrome_2": 1,
    "not_provided|not_specified|Aicardi-Goutieres_syndrome_2": 3,
    "Aicardi-Goutieres_syndrome_2|Aicardi_Goutieres_syndrome|not_provided": 1,
    "RNASEH2B-related_disorder|not_provided|Aicardi-Goutieres_syndrome_2": 1,
    "Aicardi-Goutieres_syndrome_2|not_specified": 4,
    "not_provided|Aicardi-Goutieres_syndrome_2|Inborn_genetic_diseases": 1,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_2": 1,
    "not_provided|Aicardi-Goutieres_syndrome_1|Aicardi-Goutieres_syndrome_2": 1,
    "RNASEH2B-related_disorder|Aicardi-Goutieres_syndrome_2": 1,
    "RNASEH2B-related_disorder|Inborn_genetic_diseases|not_provided|Aicardi_Goutieres_syndrome|Hereditary_spastic_paraplegia|Autism_spectrum_disorder|Aicardi-Goutieres_syndrome_2|Abnormality_of_the_nervous_system|Cerebral_palsy": 1,
    "Inborn_genetic_diseases|not_provided|Aicardi-Goutieres_syndrome_2": 1,
    "Aicardi-Goutieres_syndrome_2|not_provided|Aicardi_Goutieres_syndrome": 1,
    "not_specified|not_provided|Aicardi-Goutieres_syndrome_2": 2,
    "not_provided|Aicardi-Goutieres_syndrome_2|RNASEH2B-related_disorder": 1,
    "not_specified|Aicardi-Goutieres_syndrome_2|not_provided": 1,
    "Aicardi_Goutieres_syndrome|not_specified|Aicardi-Goutieres_syndrome_2|not_provided": 1,
    "INTS6-related_disorder": 10,
    "INTS6-associated_neurodevelopmental_disorder": 1,
    "Wilson_disease|not_provided": 124,
    "not_provided|Wilson_disease": 151,
    "not_specified|not_provided|Wilson_disease": 16,
    "Wilson_disease|not_specified": 41,
    "not_provided|not_specified|Wilson_disease": 10,
    "Inborn_genetic_diseases|Wilson_disease": 40,
    "Wilson_disease|Inborn_genetic_diseases": 31,
    "Inborn_genetic_diseases|not_specified|not_provided|Wilson_disease": 9,
    "Inborn_genetic_diseases|Wilson_disease|not_specified|not_provided": 4,
    "not_specified|Wilson_disease": 42,
    "not_specified|Wilson_disease|not_provided": 9,
    "ATP7B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Wilson_disease|See_cases": 1,
    "not_provided|ATP7B-related_disorder|Wilson_disease": 4,
    "not_provided|Wilson_disease|not_specified|Inborn_genetic_diseases": 1,
    "Wilson_disease|ATP7B-related_disorder": 6,
    "ATP7B-related_disorder": 9,
    "not_provided|Wilson_disease|Inborn_genetic_diseases": 3,
    "Wilson_disease|not_provided|Inborn_genetic_diseases": 1,
    "ATP7B-related_disorder|Wilson_disease|not_provided|Inborn_genetic_diseases": 1,
    "ATP7B-related_disorder|Wilson_disease": 7,
    "not_provided|not_specified|Wilson_disease|ATP7B-related_disorder": 1,
    "Wilson_disease|ATP7B-related_disorder|not_provided": 3,
    "ATP7B-related_disorder|Inborn_genetic_diseases|not_provided|Wilson_disease": 7,
    "Inborn_genetic_diseases|not_provided|Wilson_disease": 21,
    "Wilson_disease|Inborn_genetic_diseases|not_provided": 1,
    "Wilson_disease|not_provided|not_specified": 6,
    "Wilson_disease|not_specified|not_provided": 9,
    "not_specified|Wilson_disease|ATP7B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Wilson_disease|not_provided|ATP7B-related_disorder": 1,
    "not_provided|Wilson_disease|not_specified": 3,
    "Wilson_disease|Inborn_genetic_diseases|not_specified|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|Wilson_disease|ATP7B-related_disorder": 1,
    "ATP7B-related_disorder|Inborn_genetic_diseases|not_provided|Wilson_disease|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Wilson_disease": 3,
    "Wilson_disease|not_specified|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|not_specified|Inborn_genetic_diseases|Wilson_disease": 1,
    "not_specified|not_provided|Wilson_disease|Inborn_genetic_diseases": 2,
    "ATP7B-related_disorder|Wilson_disease|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Wilson_disease|not_specified": 1,
    "Inborn_genetic_diseases|Wilson_disease|not_provided": 3,
    "ATP7B-related_disorder|not_specified|Wilson_disease": 1,
    "Wilson_disease|ATP7B-related_disorder|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Wilson_disease": 3,
    "Wilson_disease|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "ATP7B-related_disorder|not_provided|Wilson_disease": 8,
    "Inborn_genetic_diseases|not_specified|Wilson_disease": 3,
    "not_provided|Wilson_disease|Abnormality_of_metabolism/homeostasis": 1,
    "not_provided|Wilson_disease|Epileptic_encephalopathy": 1,
    "not_specified|Wilson_disease|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Wilson_disease|not_provided": 2,
    "ATP7B-related_disorder|not_provided|Wilson_disease|Inborn_genetic_diseases": 1,
    "Kayser-Fleischer_ring|Hand_tremor|Wilson_disease": 1,
    "Inborn_genetic_diseases|ATP7B-related_disorder|not_specified|not_provided|Wilson_disease": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Wilson_disease|ATP7B-related_disorder": 1,
    "Hearing_loss|_autosomal_recessive_109|ATP7B-related_disorder|Inborn_genetic_diseases|not_provided|Wilson_disease": 1,
    "not_provided|not_specified|Wilson_disease|Inborn_genetic_diseases": 1,
    "Wilson_disease|ATP7B-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Wilson_disease": 1,
    "not_provided|Wilson_disease|ATP7B-related_disorder": 2,
    "Wilson_disease|not_provided|ATP7B-related_disorder": 1,
    "ATP7B-related_disorder|not_specified|Wilson_disease|not_provided": 1,
    "Inborn_genetic_diseases|ATP7B-related_disorder|not_provided|Wilson_disease": 1,
    "Wilson_disease|ATP7B-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Wilson_disease": 4,
    "Inborn_genetic_diseases|Wilson_disease|not_specified": 1,
    "not_provided|ATP7B-related_disorder|Inborn_genetic_diseases|Wilson_disease": 1,
    "Wilson_disease|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "not_specified|Wilson_disease|Inborn_genetic_diseases": 1,
    "not_provided|ATP7B-related_disorder|Wilson_disease|Inborn_genetic_diseases": 1,
    "ATP7B-related_disorder|not_specified|not_provided|Wilson_disease": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Wilson_disease|Epileptic_encephalopathy": 1,
    "not_specified|Inborn_genetic_diseases|ATP7B-related_disorder|Wilson_disease|not_provided": 1,
    "ATP7B-related_disorder|Wilson_disease|Inborn_genetic_diseases|not_provided": 2,
    "ATP7B-related_disorder|Wilson_disease|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Spastic_ataxia|not_provided|Wilson_disease": 1,
    "ATP7B-related_disorder|Inborn_genetic_diseases|not_specified|Wilson_disease|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_93|not_provided|Wilson_disease": 1,
    "ATP7B-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Wilson_disease": 1,
    "Inborn_genetic_diseases|Wilson_disease|ATP7B-related_disorder": 1,
    "not_specified|ATP7B-related_disorder|not_provided|Wilson_disease": 1,
    "Wilson_disease|Inborn_genetic_diseases|ATP7B-related_disorder|not_provided": 1,
    "not_provided|not_specified|Wilson_disease|ATP7B-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Wilson_disease": 1,
    "not_provided|Wilson_disease|See_cases|ATP7B-related_disorder": 1,
    "Intellectual_disability|_Wolff_type|ATP7B-related_disorder|not_provided|Wilson_disease": 1,
    "Anhaptoglobinemia": 4,
    "Inborn_genetic_diseases|not_specified|ATP7B-related_disorder|not_provided|Wilson_disease": 1,
    "Wilson_disease|not_specified|Inborn_genetic_diseases": 1,
    "Wilson_disease|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "ATP7B-related_disorder|Wilson_disease|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|ATP7B-related_disorder|not_specified|Wilson_disease": 1,
    "not_specified|Congenital_disorder_of_glycosylation|not_provided|Wilson_disease": 1,
    "Wilson_disease|not_provided|not_specified|ALG11-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation": 1,
    "not_specified|not_provided|Wilson_disease|ALG11-congenital_disorder_of_glycosylation": 1,
    "ALG11-related_disorder": 3,
    "ALG11-congenital_disorder_of_glycosylation": 72,
    "Inborn_genetic_diseases|ALG11-congenital_disorder_of_glycosylation": 4,
    "ALG11-congenital_disorder_of_glycosylation|not_provided": 13,
    "not_provided|ALG11-congenital_disorder_of_glycosylation": 9,
    "not_provided|ALG11-congenital_disorder_of_glycosylation|not_specified": 1,
    "not_provided|not_specified|ALG11-congenital_disorder_of_glycosylation": 2,
    "not_provided|ALG11-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|ALG11-congenital_disorder_of_glycosylation": 2,
    "ALG11-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 4,
    "ALG11-congenital_disorder_of_glycosylation|ALG11-related_disorder": 3,
    "ALG11-related_disorder|not_provided|ALG11-congenital_disorder_of_glycosylation": 1,
    "not_specified|ALG11-congenital_disorder_of_glycosylation|not_provided|ALG11-related_disorder": 1,
    "not_specified|ALG11-congenital_disorder_of_glycosylation": 1,
    "not_specified|not_provided|ALG11-congenital_disorder_of_glycosylation": 1,
    "THSD1-related_disorder": 20,
    "not_provided|not_specified|Lymphatic_malformation_13": 1,
    "not_provided|THSD1-related_disorder": 2,
    "Lymphatic_malformation_13": 3,
    "Aneurysm|_intracranial_berry|_12": 2,
    "THSD1-related_disorder|not_provided": 1,
    "Lymphatic_malformation_13|Non-immune_hydrops_fetalis|not_provided": 1,
    "Lymphatic_malformation_13|Non-immune_hydrops_fetalis": 1,
    "DIAPH3-related_disorder": 6,
    "Autosomal_dominant_auditory_neuropathy_1|not_provided": 6,
    "DIAPH3-related_disorder|not_provided|not_specified": 1,
    "not_provided|DIAPH3-related_disorder": 8,
    "not_provided|DIAPH3-related_disorder|not_specified": 3,
    "not_provided|Autosomal_dominant_auditory_neuropathy_1": 2,
    "not_specified|not_provided|Autosomal_dominant_auditory_neuropathy_1": 2,
    "Autosomal_dominant_auditory_neuropathy_1": 9,
    "not_specified|DIAPH3-related_disorder|not_provided": 2,
    "DIAPH3-related_disorder|not_provided": 5,
    "Autosomal_dominant_auditory_neuropathy_1|DIAPH3-related_disorder|not_provided": 1,
    "DIAPH3-related_disorder|not_provided|Autosomal_dominant_auditory_neuropathy_1": 2,
    "Autosomal_dominant_auditory_neuropathy_1|not_specified|not_provided": 1,
    "PCDH9-related_disorder": 6,
    "KLHL1-related_disorder|not_provided": 1,
    "KLHL1-related_disorder": 2,
    "KLHL1-related_disorder|not_specified": 2,
    "ATXN8OS-related_disorder": 10,
    "DIS3-related_disorder": 2,
    "not_specified|DIS3-related_disorder": 1,
    "DIS3-related_disorder|not_provided": 1,
    "not_specified|PIBF1-related_disorder|not_provided": 1,
    "not_provided|PIBF1-related_disorder": 4,
    "PIBF1-related_disorder": 12,
    "not_provided|Joubert_syndrome_33": 4,
    "Joubert_syndrome_33": 11,
    "Joubert_syndrome_33|Inborn_genetic_diseases": 2,
    "Joubert_syndrome_33|PIBF1-related_disorder": 2,
    "PIBF1-related_disorder|Inborn_genetic_diseases|Joubert_syndrome_33": 1,
    "Joubert_syndrome_33|Joubert_syndrome|not_provided|not_specified": 1,
    "Joubert_syndrome_33|not_provided|not_specified": 1,
    "Joubert_syndrome_33|not_provided": 4,
    "Cephalocele|Joubert_syndrome_33|Dandy-Walker_syndrome": 1,
    "PIBF1-related_disorder|Joubert_syndrome_33": 1,
    "Dandy-Walker_syndrome|Joubert_syndrome_33|Cephalocele": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_33": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_33": 1,
    "Joubert_syndrome_33|not_provided|PIBF1-related_disorder": 1,
    "Dilated_cardiomyopathy_1FF": 6,
    "TBC1D4-related_disorder": 9,
    "not_specified|not_provided|TBC1D4-related_disorder": 3,
    "not_specified|Insulin_resistance": 1,
    "Diabetes_mellitus|_noninsulin-dependent|_5": 1,
    "TYPE_2_DIABETES_MELLITUS_5|_SUSCEPTIBILITY_TO": 1,
    "TBC1D4-related_disorder|not_specified|not_provided": 1,
    "not_provided|TBC1D4-related_disorder|not_specified": 1,
    "TBC1D4-related_disorder|not_specified": 1,
    "LMO7-related_disorder": 12,
    "LMO7-related_disorder|not_provided": 1,
    "not_specified|LMO7-related_disorder": 1,
    "Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome": 4,
    "not_specified|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis_5": 79,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 9,
    "CLN5-related_disorder|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 4,
    "Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis": 33,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 22,
    "Neuronal_ceroid_lipofuscinosis_5|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|not_provided|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Inborn_genetic_diseases|CLN5-related_disorder|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 1,
    "not_specified|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 2,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|not_provided|Inborn_genetic_diseases|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|not_provided|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive": 1,
    "CLN5-related_disorder|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|not_provided": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided": 1,
    "CLN5-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis": 5,
    "not_specified|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_5|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis": 2,
    "Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided|not_specified|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_5": 2,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_5|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_5|Pontocerebellar_hypoplasia_type_2D": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Neuronal_ceroid_lipofuscinosis_5|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 3,
    "Neuronal_ceroid_lipofuscinosis_5|not_provided|Neuronal_ceroid_lipofuscinosis": 6,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|CLN5-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive": 1,
    "Neuronal_ceroid_lipofuscinosis|CLN5-related_disorder": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|not_provided": 2,
    "Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Intellectual_disability|Neuronal_ceroid_lipofuscinosis": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_5|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases": 2,
    "Neuronal_ceroid_lipofuscinosis_5|not_provided|not_specified|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_5|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_5|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_5|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_5|not_specified|not_provided": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_5": 1,
    "not_provided|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_5": 4,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided|Neuronal_ceroid_lipofuscinosis_5": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_5": 6,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_5|not_provided": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_5": 1,
    "FBXL3-related_disorder": 3,
    "Intellectual_disability|_short_stature|_facial_anomalies|_and_joint_dislocations": 4,
    "Intellectual_disability|_short_stature|_facial_anomalies|_and_joint_dislocations|not_provided": 1,
    "MYCBP2-related_disorder": 57,
    "not_provided|MYCBP2-related_disorder": 13,
    "MYCBP2-related_disorder|Inborn_genetic_diseases": 1,
    "MYCBP2-related_neurodevelopmental_disorder": 1,
    "MYCBP2-related_disorder|not_provided": 3,
    "MYCBP2-related_developmental_delay_with_corpus_callosum_defects": 2,
    "not_specified|MYCBP2-related_disorder": 1,
    "MYCBP2-associated_neurodevelopmental_disorder": 1,
    "MYCBP2-associated_disorder|not_provided": 1,
    "SLAIN1-related_disorder": 6,
    "Hirschsprung_disease|_susceptibility_to|_2": 53,
    "not_specified|not_provided|Hirschsprung_disease|_susceptibility_to|_2": 3,
    "Hirschsprung_disease|_susceptibility_to|_2|not_provided": 8,
    "Hirschsprung_Disease|_Recessive|Waardenburg_syndrome": 2,
    "not_provided|EDNRB-related_disorder": 3,
    "Hirschsprung_Disease|_Recessive|Waardenburg_syndrome|Inborn_genetic_diseases|not_specified|ABCD_syndrome|Hirschsprung_disease|_susceptibility_to|_2|Waardenburg_syndrome_type_4A|not_provided": 1,
    "Waardenburg_syndrome_type_4A": 21,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_2": 2,
    "not_specified|Hirschsprung_disease|_susceptibility_to|_2|not_provided": 1,
    "not_provided|ABCD_syndrome|Waardenburg_syndrome_type_4A|Hirschsprung_disease|_susceptibility_to|_2": 1,
    "Hirschsprung_disease|_susceptibility_to|_2|not_specified": 1,
    "EDNRB-related_disorder": 7,
    "Inborn_genetic_diseases|not_provided|Hirschsprung_disease|_susceptibility_to|_2": 1,
    "ABCD_syndrome|Hirschsprung_disease|_susceptibility_to|_2|Waardenburg_syndrome_type_4A": 2,
    "Inborn_genetic_diseases|Hearing_impairment|Aganglionosis|_total_intestinal": 1,
    "not_provided|Waardenburg_syndrome_type_4A|Inborn_genetic_diseases": 1,
    "Waardenburg_syndrome_type_4A|Hirschsprung_disease|_susceptibility_to|_2|Waardenburg_syndrome_type_2A|not_provided|not_specified|ABCD_syndrome|Mitochondrial_DNA_depletion_syndrome_12A_(cardiomyopathic_type)|_autosomal_dominant": 1,
    "not_provided|Waardenburg_syndrome_type_4A": 1,
    "Waardenburg_syndrome_type_4A|Hirschsprung_disease|_susceptibility_to|_2|not_provided": 1,
    "not_provided|ABCD_syndrome|Hirschsprung_disease|_susceptibility_to|_2|Waardenburg_syndrome_type_4A": 1,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_2|not_specified": 2,
    "Waardenburg_syndrome_type_4A|not_provided": 1,
    "not_specified|not_provided|EDNRB-related_disorder": 2,
    "ABCD_syndrome|Waardenburg_syndrome_type_4A|not_provided": 1,
    "not_provided|not_specified|Hirschsprung_disease|_susceptibility_to|_2": 2,
    "Hearing_impairment|Aganglionosis|_total_intestinal|Hirschsprung_disease|_susceptibility_to|_2|Waardenburg_syndrome_type_4A|Inborn_genetic_diseases|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Waardenburg_syndrome_type_4A|Hirschsprung_disease|_susceptibility_to|_2|ABCD_syndrome|not_provided|not_specified": 1,
    "EDNRB-related_disorder|Hirschsprung_disease|_susceptibility_to|_2|not_provided": 1,
    "not_provided|not_specified|Waardenburg_syndrome_type_4A|Hirschsprung_disease|_susceptibility_to|_2": 1,
    "Waardenburg_syndrome_type_4A|Waardenburg_syndrome|EDNRB-related_disorder": 1,
    "Ataxia|_intention_tremor|_and_hypotonia_syndrome|_childhood-onset": 7,
    "POU4F1-related_disorder": 4,
    "Ataxia|_intention_tremor|_and_hypotonia_syndrome|_childhood-onset|not_provided": 2,
    "POU4F1-related_disorder|not_provided|not_specified": 1,
    "not_provided|POU4F1-related_disorder": 1,
    "IgA_nephropathy|_susceptibility_to|_3": 3,
    "SPRY2-related_disorder": 4,
    "SLITRK1-related_disorder": 3,
    "Tourette_syndrome|Trichotillomania": 5,
    "Tourette_syndrome|not_provided": 4,
    "not_specified|Tourette_syndrome": 1,
    "not_provided|Tourette_syndrome|not_specified": 1,
    "Trichotillomania": 1,
    "not_provided|SLITRK6-related_disorder": 1,
    "SLITRK6-related_disorder|Inborn_genetic_diseases|not_provided|High_myopia-sensorineural_deafness_syndrome": 1,
    "High_myopia-sensorineural_deafness_syndrome|not_provided": 1,
    "SLITRK6-related_disorder|not_provided|not_specified": 2,
    "not_provided|High_myopia-sensorineural_deafness_syndrome|not_specified": 1,
    "SLITRK6-related_disorder|not_provided": 4,
    "SLITRK6-related_disorder": 3,
    "not_specified|not_provided|High_myopia-sensorineural_deafness_syndrome": 1,
    "SLITRK6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Hearing_impairment|not_provided|Inborn_genetic_diseases": 2,
    "SLITRK6-related_disorder|not_provided|High_myopia-sensorineural_deafness_syndrome": 1,
    "High_myopia-sensorineural_deafness_syndrome": 4,
    "not_provided|SLITRK6-related_disorder|not_specified": 1,
    "not_provided|not_specified|High_myopia-sensorineural_deafness_syndrome": 1,
    "not_specified|SLITRK6-related_disorder|not_provided": 1,
    "not_specified|not_provided|SLITRK6-related_disorder": 1,
    "not_provided|not_specified|SLITRK6-related_disorder": 1,
    "SLITRK5-related_disorder": 8,
    "not_specified|SLITRK5-related_disorder": 1,
    "MIR17HG-related_disorder": 24,
    "GPC5-related_disorder|not_specified": 1,
    "GPC5-related_disorder": 3,
    "Autosomal_recessive_omodysplasia|not_provided": 11,
    "Autosomal_recessive_omodysplasia": 92,
    "Autosomal_recessive_omodysplasia|not_provided|not_specified|GPC6-related_disorder": 1,
    "Autosomal_recessive_omodysplasia|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|GPC6-related_disorder": 2,
    "not_specified|not_provided|Autosomal_recessive_omodysplasia": 1,
    "GPC6-related_disorder|Autosomal_recessive_omodysplasia": 1,
    "GPC6-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_omodysplasia|not_provided": 1,
    "not_provided|Autosomal_recessive_omodysplasia": 14,
    "Autosomal_recessive_omodysplasia|Inborn_genetic_diseases": 2,
    "Omodysplasia": 6,
    "Omodysplasia|not_provided": 1,
    "Albinism|Oculocutaneous_albinism_type_8": 1,
    "DCT-related_disorder": 2,
    "Inborn_genetic_diseases|DCT-related_disorder": 1,
    "Oculocutaneous_albinism_type_8|Albinism": 2,
    "TGDS-related_disorder|not_provided": 3,
    "Catel-Manzke_syndrome|not_provided": 2,
    "TGDS-related_disorder|Catel-Manzke_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Catel-Manzke_syndrome": 1,
    "TGDS-related_disorder": 2,
    "GPR180-related_disorder": 10,
    "ABCC4-related_disorder": 3,
    "HELIX_syndrome": 8,
    "CLDN10-related_disorder": 2,
    "Lower_limb_muscle_weakness|Hypokalemia|Hypomagnesemia|Inborn_genetic_diseases": 1,
    "DZIP1-related_disorder": 1,
    "Spermatogenic_failure_47": 3,
    "DZIP1-related_disorder|Mitral_valve_prolapse|_myxomatous_3|Spermatogenic_failure_47": 1,
    "not_provided|DNAJC3-related_disorder": 3,
    "DNAJC3-related_disorder": 4,
    "DNAJC3-related_disorder|not_provided": 1,
    "Juvenile-onset_diabetes_mellitus-central_and_peripheral_neurodegeneration_syndrome|Prostate_cancer": 1,
    "DNAJC3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Juvenile-onset_diabetes_mellitus-central_and_peripheral_neurodegeneration_syndrome": 1,
    "Juvenile-onset_diabetes_mellitus-central_and_peripheral_neurodegeneration_syndrome|not_provided": 2,
    "not_specified|Nephrolithiasis|_calcium_oxalate|_2|_with_or_without_nephrocalcinosis": 1,
    "Nephrolithiasis|_calcium_oxalate|_2|_with_or_without_nephrocalcinosis": 4,
    "Holoprosencephaly_5": 287,
    "ZIC2-related_disorder": 13,
    "Holoprosencephaly_5|ZIC2-related_disorder": 6,
    "not_specified|Holoprosencephaly_5": 3,
    "Holoprosencephaly_5|Inborn_genetic_diseases": 7,
    "Holoprosencephaly_5|not_provided": 11,
    "not_provided|Holoprosencephaly_5|not_specified": 1,
    "ZIC2-related_disorder|Holoprosencephaly_5": 6,
    "Holoprosencephaly_5|not_specified": 5,
    "Inborn_genetic_diseases|Holoprosencephaly_5": 7,
    "not_provided|Holoprosencephaly_5": 9,
    "Holoprosencephaly_5|not_provided|not_specified": 2,
    "not_provided|not_specified|Holoprosencephaly_5": 3,
    "Holoprosencephaly_5|not_specified|not_provided": 1,
    "Microcephaly|Holoprosencephaly_sequence": 1,
    "Inborn_genetic_diseases|not_provided|Holoprosencephaly_5": 1,
    "ZIC2-related_disorder|Holoprosencephaly_5|not_provided": 1,
    "not_provided|Holoprosencephaly_5|ZIC2-related_disorder": 1,
    "Holoprosencephaly_1|not_specified": 1,
    "not_provided|Propionic_acidemia|Pontocerebellar_hypoplasia_type_2D": 1,
    "not_provided|Inborn_genetic_diseases|Propionic_acidemia": 1,
    "not_provided|Propionic_acidemia|PCCA-related_disorder": 1,
    "PCCA-related_disorder": 5,
    "Propionic_acidemia|not_specified|not_provided": 3,
    "Propionic_acidemia|PCCA-related_disorder": 4,
    "not_specified|Propionic_acidemia|not_provided": 3,
    "PCCA-related_disorder|Propionic_acidemia|not_provided": 2,
    "Inborn_genetic_diseases|Propionic_acidemia|PCCA-related_disorder": 1,
    "PCCA-related_disorder|not_provided|Propionic_acidemia": 4,
    "Propionic_acidemia|not_provided|PCCA-related_disorder": 2,
    "Propionic_acidemia|PCCA-related_disorder|not_provided": 2,
    "Propionic_acidemia|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Propionic_acidemia|PCCA-related_disorder": 1,
    "PCCA-related_disorder|Propionic_acidemia": 1,
    "Propionic_acidemia|not_specified|PCCA-related_disorder": 1,
    "not_provided|Propionic_acidemia|PCCA-related_disorder|not_specified": 1,
    "Worster-Drought_syndrome": 1,
    "Hearing_loss|_autosomal_recessive_122": 2,
    "not_provided|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 6,
    "not_provided|Inborn_genetic_diseases|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 2,
    "not_provided|NALCN-related_disorder": 14,
    "NALCN-related_disorder|not_provided": 18,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|NALCN-related_disorder": 3,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 37,
    "not_provided|Inborn_genetic_diseases|NALCN-related_disorder": 1,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided": 9,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|NALCN-related_disorder": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies": 1,
    "not_specified|not_provided|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "NALCN-related_disorder": 8,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|not_provided": 5,
    "not_provided|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "not_specified|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Intellectual_disability_with_episodic_ataxia_and_congenital_arthrogryposis": 1,
    "Strabismus|Seizure|Abnormal_pattern_of_respiration|Cachexia|Intellectual_disability|_severe": 1,
    "Inborn_genetic_diseases|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided|NALCN-related_disorder": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 5,
    "not_specified|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|NALCN-related_disorder": 1,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 2,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|NALCN-related_disorder|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 1,
    "not_specified|not_provided|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 1,
    "Inborn_genetic_diseases|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 2,
    "not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 3,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|NALCN-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "NALCN-related_disorder|not_provided|not_specified": 1,
    "Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|not_provided|Inborn_genetic_diseases": 1,
    "NALCN-related_disorder|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_specified|not_provided": 1,
    "not_specified|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided|See_cases": 1,
    "NALCN-related_disorder|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay": 1,
    "Arthrogryposis_syndrome|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided": 1,
    "not_provided|not_specified|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "Abnormality_of_the_nervous_system|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided": 2,
    "NALCN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|not_provided": 1,
    "NALCN-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_contractures_of_the_limbs_and_face|_hypotonia|_and_developmental_delay|Hypotonia|_infantile|_with_psychomotor_retardation_and_characteristic_facies_1": 1,
    "Spinocerebellar_ataxia_type_27": 34,
    "not_provided|Spinocerebellar_ataxia_type_27": 5,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_27": 2,
    "not_specified|Spinocerebellar_ataxia_type_27|FGF14-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_27": 1,
    "Spinocerebellar_ataxia_type_27|not_provided": 3,
    "FGF14-related_disorder|not_provided|not_specified": 1,
    "FGF14-related_disorder": 4,
    "Spinocerebellar_ataxia_27A|Spinocerebellar_ataxia_type_27": 1,
    "Spinocerebellar_ataxia_27A": 9,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_27|FGF14-related_disorder": 1,
    "not_provided|Spinocerebellar_ataxia_27A": 1,
    "FGF14-related_disorder|Spinocerebellar_ataxia_type_27": 1,
    "Spinocerebellar_ataxia_27A|Spinocerebellar_ataxia_27B|_late-onset|not_provided|FGF14-related_disorder|Spinocerebellar_ataxia_type_27|not_specified": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_27|Cerebellar_ataxia": 1,
    "Spinocerebellar_ataxia_27B|_late-onset": 1,
    "not_provided|FGF14-related_disorder": 1,
    "TPP2-related_disorder": 3,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 582,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|Inborn_genetic_diseases": 22,
    "not_provided|Immunodeficiency_78_with_autoimmunity_and_developmental_delay": 1,
    "Inborn_genetic_diseases|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 28,
    "TPP2-related_disorder|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_provided": 6,
    "not_provided|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 5,
    "Immunodeficiency_78_with_autoimmunity_and_developmental_delay": 5,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_specified|not_provided": 3,
    "not_specified|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 2,
    "TPP2-related_disorder|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 8,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_provided|not_specified": 2,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|Immunodeficiency_78_with_autoimmunity_and_developmental_delay": 2,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|Immunodeficiency_78_with_autoimmunity_and_developmental_delay|not_provided": 1,
    "Immunodeficiency_78_with_autoimmunity_and_developmental_delay|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 1,
    "Immunodeficiency_78_with_autoimmunity_and_developmental_delay|Inborn_genetic_diseases|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency": 1,
    "Immunodeficiency_78_with_autoimmunity_and_developmental_delay|Thrombocytopenia|Global_developmental_delay|Recurrent_lower_respiratory_tract_infections|Recurrent_upper_respiratory_tract_infections|Acute_otitis_media|Cutis_marmorata": 1,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_provided|Immunodeficiency_78_with_autoimmunity_and_developmental_delay": 1,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|TPP2-related_disorder": 3,
    "Immunodeficiency_78_with_autoimmunity_and_developmental_delay|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_provided": 2,
    "Evans_syndrome|_immunodeficiency|_and_premature_immunosenescence_associated_with_tripeptidyl-peptidase_II_deficiency|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|_group_G": 17,
    "Xeroderma_pigmentosum|_group_G": 40,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3": 17,
    "Cerebrooculofacioskeletal_syndrome_3|Inborn_genetic_diseases|not_specified|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G|Hereditary_cancer-predisposing_syndrome": 1,
    "Xeroderma_pigmentosum|_group_G|not_provided": 6,
    "Cerebrooculofacioskeletal_syndrome_3": 12,
    "Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 3,
    "not_specified|not_provided|Xeroderma_pigmentosum|_group_G": 6,
    "ERCC5-related_disorder": 5,
    "Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "not_specified|Xeroderma_pigmentosum|_group_G": 1,
    "Xeroderma_pigmentosum_group_G/Cockayne_syndrome": 3,
    "not_provided|not_specified|Xeroderma_pigmentosum|_group_G": 2,
    "Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G": 2,
    "Xeroderma_pigmentosum-Cockayne_syndrome_complex": 1,
    "not_specified|Xeroderma_pigmentosum|_group_G|not_provided": 2,
    "Cerebrooculofacioskeletal_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "not_provided|ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Inborn_genetic_diseases|Cerebrooculofacioskeletal_syndrome_3": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_3": 3,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|not_specified|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|ERCC5-related_disorder|not_specified": 1,
    "ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G": 1,
    "Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "not_provided|ERCC5-related_disorder|not_specified|Xeroderma_pigmentosum|_group_G": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Xeroderma_pigmentosum|_group_G": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 1,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum|_group_G|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3": 2,
    "not_provided|BIVM-ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 1,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|not_provided": 1,
    "ERCC5-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BIVM-ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G": 1,
    "not_specified|not_provided|Ovarian_cancer": 1,
    "Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G|Xeroderma_pigmentosum": 2,
    "not_provided|Cerebrooculofacioskeletal_syndrome_3|not_specified": 1,
    "Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G|not_specified|not_provided": 3,
    "Xeroderma_pigmentosum|_group_G|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "BIVM-ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|_group_G|not_specified": 1,
    "Cerebrooculofacioskeletal_syndrome_3|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_G": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|ERCC5-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 1,
    "ERCC5-related_disorder|not_specified|Cerebrooculofacioskeletal_syndrome_3": 1,
    "Cerebrooculofacioskeletal_syndrome_3|ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "BIVM-ERCC5-related_disorder|Cerebrooculofacioskeletal_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "Xeroderma_pigmentosum_group_G/Cockayne_syndrome|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|Hereditary_cancer-predisposing_syndrome": 2,
    "ERCC5-related_disorder|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "BIVM-ERCC5-related_disorder|not_provided": 1,
    "not_specified|Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Xeroderma_pigmentosum|Cerebrooculofacioskeletal_syndrome_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BIVM-ERCC5-related_disorder": 1,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|_group_G|Hereditary_cancer-predisposing_syndrome": 1,
    "Xeroderma_pigmentosum|_group_G|Inborn_genetic_diseases|not_specified": 1,
    "Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|not_provided": 1,
    "not_provided|BIVM-ERCC5-related_disorder|ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 1,
    "not_specified|BIVM-ERCC5-related_disorder|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G|not_specified": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_G|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 1,
    "Polyneuropathy|Cerebellar_atrophy|Dysarthria|Pectus_excavatum|Spastic_paraplegia|Cognitive_impairment|Abnormal_corpus_callosum_morphology|Pes_cavus": 1,
    "not_specified|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_G": 1,
    "Cerebrooculofacioskeletal_syndrome_3|not_provided|not_specified|BIVM-ERCC5-related_disorder": 1,
    "not_provided|Xeroderma_pigmentosum|_group_G|ERCC5-related_disorder": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G": 1,
    "not_specified|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_G": 1,
    "ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G|Cerebrooculofacioskeletal_syndrome_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum|_group_G|Inborn_genetic_diseases": 1,
    "Cerebrooculofacioskeletal_syndrome_3|not_specified|Xeroderma_pigmentosum|_group_G|not_provided": 1,
    "ERCC5-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "Xeroderma_pigmentosum|_group_G|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|BIVM-ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G|Inborn_genetic_diseases": 1,
    "BIVM-ERCC5-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Xeroderma_pigmentosum|_group_G": 1,
    "BIVM-ERCC5-related_disorder|Xeroderma_pigmentosum|_group_G|not_provided": 1,
    "Xeroderma_pigmentosum|_group_G|Ovarian_cancer": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_3|Xeroderma_pigmentosum|_group_G|Hereditary_cancer-predisposing_syndrome": 1,
    "SLC10A2-related_disorder": 12,
    "SLC10A2-related_disorder|not_provided": 16,
    "not_provided|SLC10A2-related_disorder": 17,
    "not_provided|not_specified|SLC10A2-related_disorder": 1,
    "Bile_acid_malabsorption|_primary|_1|not_provided": 3,
    "not_provided|Bile_acid_malabsorption|_primary|_1|SLC10A2-related_disorder": 2,
    "SLC10A2-related_disorder|not_provided|Bile_acid_malabsorption|_primary|_1": 1,
    "not_provided|SLC10A2-related_disorder|not_specified": 3,
    "not_provided|SLC10A2-related_disorder|Bile_acid_malabsorption|_primary|_1": 1,
    "not_provided|Bile_acid_malabsorption|_primary|_1": 5,
    "Bile_acid_malabsorption|_primary|_1": 1,
    "not_specified|not_provided|Bile_acid_malabsorption|_primary|_1": 1,
    "Bile_acid_malabsorption|_primary|_1|not_specified|not_provided": 1,
    "SLC10A2-related_disorder|not_specified|not_provided": 1,
    "SLC10A2-related_disorder|Bile_acid_malabsorption|_primary|_1|not_provided": 1,
    "Bile_acid_malabsorption|_primary|_1|SLC10A2-related_disorder|not_provided": 1,
    "SLC10A2-related_disorder|not_provided|not_specified": 1,
    "EFNB2-related_neurodevelopmental_disorder": 1,
    "EFNB2-related_disorder": 5,
    "ARGLU1-related_disorder": 3,
    "DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 32,
    "DNA_ligase_IV_deficiency|not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 2,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|DNA_ligase_IV_deficiency": 15,
    "DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 7,
    "not_provided|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 5,
    "DNA_ligase_IV_deficiency|LIG4-related_disorder|not_provided": 1,
    "DNA_ligase_IV_deficiency": 499,
    "DNA_ligase_IV_deficiency|Inborn_genetic_diseases": 13,
    "DNA_ligase_IV_deficiency|LIG4-related_disorder": 2,
    "not_provided|DNA_ligase_IV_deficiency": 10,
    "Severe_combined_immunodeficiency_disease|LIG4-related_disorder|not_provided|DNA_ligase_IV_deficiency": 1,
    "DNA_ligase_IV_deficiency|Multiple_myeloma": 8,
    "Inborn_genetic_diseases|DNA_ligase_IV_deficiency": 20,
    "LIG4-related_disorder|not_provided|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Multiple_myeloma|not_specified": 1,
    "DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified": 1,
    "DNA_ligase_IV_deficiency|not_provided": 15,
    "not_specified|DNA_ligase_IV_deficiency|not_provided": 4,
    "prenatal_LIG4_syndrome_with_aqueductal_stenosis|Multiple_myeloma|DNA_ligase_IV_deficiency|LIG4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified|DNA_ligase_IV_deficiency|Inborn_genetic_diseases": 1,
    "DNA_ligase_IV_deficiency|Multiple_myeloma|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "not_specified|DNA_ligase_IV_deficiency": 4,
    "LIG4-related_disorder": 5,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Inborn_genetic_diseases|DNA_ligase_IV_deficiency|not_specified": 1,
    "LIG4-related_disorder|DNA_ligase_IV_deficiency": 4,
    "DNA_ligase_IV_deficiency|LIG4-related_disorder|not_provided|Inborn_genetic_diseases|Multiple_myeloma": 1,
    "not_specified|DNA_ligase_IV_deficiency|Inborn_genetic_diseases": 1,
    "DNA_ligase_IV_deficiency|Multiple_myeloma|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 2,
    "not_provided|not_specified|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "DNA_ligase_IV_deficiency|not_provided|Multiple_myeloma": 1,
    "Multiple_myeloma|DNA_ligase_IV_deficiency|not_provided": 2,
    "DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Multiple_myeloma": 1,
    "Multiple_myeloma|DNA_ligase_IV_deficiency": 1,
    "not_specified|not_provided|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "Papillary_thyroid_carcinoma": 1,
    "not_provided|LIG4-related_disorder|DNA_ligase_IV_deficiency": 1,
    "Inborn_genetic_diseases|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 2,
    "not_provided|prenatal_LIG4_syndrome_with_aqueductal_stenosis|DNA_ligase_IV_deficiency|Multiple_myeloma": 1,
    "DNA_ligase_IV_deficiency|Multiple_myeloma|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|DNA_ligase_IV_deficiency": 2,
    "DNA_ligase_IV_deficiency|not_specified|Multiple_myeloma": 1,
    "not_provided|Multiple_myeloma|DNA_ligase_IV_deficiency|LIG4-related_disorder": 1,
    "not_specified|not_provided|DNA_ligase_IV_deficiency": 2,
    "not_provided|DNA_ligase_IV_deficiency|Inborn_genetic_diseases": 1,
    "DNA_ligase_IV_deficiency|not_specified|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Multiple_myeloma": 1,
    "DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|prenatal_LIG4_syndrome_with_aqueductal_stenosis|not_provided": 1,
    "DNA_ligase_IV_deficiency|not_specified|LIG4-related_disorder|Multiple_myeloma": 1,
    "DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "DNA_ligase_IV_deficiency|Multiple_myeloma|Severe_combined_immunodeficiency_disease": 1,
    "not_provided|Severe_combined_immunodeficiency_disease|DNA_ligase_IV_deficiency": 1,
    "DNA_ligase_IV_deficiency|not_specified": 4,
    "DNA_ligase_IV_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|DNA_ligase_IV_deficiency|not_specified|LIG4-related_disorder": 1,
    "DNA_ligase_IV_deficiency|Inborn_genetic_diseases|Multiple_myeloma|not_provided": 1,
    "Inborn_genetic_diseases|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_provided": 1,
    "DNA_ligase_IV_deficiency|Multiple_myeloma|not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "not_provided|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified": 1,
    "LIG4-related_disorder|DNA_ligase_IV_deficiency|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "DNA_ligase_IV_deficiency|not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|not_specified": 1,
    "not_specified|not_provided|DNA_ligase_IV_deficiency|LIG4-related_disorder|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|Multiple_myeloma|_resistance_to|DNA_ligase_IV_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|DNA_ligase_IV_deficiency|Multiple_myeloma|_resistance_to|not_specified|not_provided": 1,
    "Severe_combined_immunodeficiency_due_to_DCLRE1C_deficiency|DNA_ligase_IV_deficiency|not_provided": 1,
    "MYO16-related_disorder|not_provided": 11,
    "MYO16-related_disorder": 30,
    "not_provided|MYO16-related_disorder": 13,
    "MYO16-associated_developmental_delay": 1,
    "not_specified|not_provided|MYO16-related_disorder": 2,
    "not_specified|MYO16-related_disorder|not_provided": 1,
    "IRS2-related_disorder": 9,
    "IRS2-related_disorder|Type_2_diabetes_mellitus": 1,
    "not_provided|IRS2-related_disorder": 1,
    "IRS2-related_disorder|not_provided": 2,
    "COL4A1-related_disorder": 48,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|not_provided": 2,
    "Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 5,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 16,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 8,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 2,
    "Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 6,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 5,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 9,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "not_provided|COL4A1_or_COL4A2-related_cerebral_small_vessel_disease|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases": 1,
    "COL4A1-related_disorder|not_provided": 23,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 11,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 78,
    "Porencephalic_cyst|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "COL4A1_or_COL4A2-related_cerebral_small_vessel_disease|not_provided": 2,
    "not_provided|COL4A1-related_disorder": 23,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided": 3,
    "COL4A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 91,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity": 3,
    "Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|COL4A1-related_disorder|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|See_cases|COL4A1-related_disorder": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 1,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity": 3,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified": 4,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 36,
    "COL4A1_or_COL4A2-related_cerebral_small_vessel_disease": 4,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 3,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|not_provided|not_specified": 1,
    "not_provided|COL4A1-related_disorder|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "not_specified|COL4A1-related_disorder|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|COL4A1-related_disorder": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|not_specified|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified": 1,
    "not_provided|COL4A1-related_disorder|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|See_cases": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Inborn_genetic_diseases|not_provided": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|not_provided": 1,
    "not_provided|not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity": 2,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Primary_membranoproliferative_glomerulonephritis|not_provided": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 2,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 6,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|COL4A1-related_disorder": 1,
    "not_provided|COL4A1_or_COL4A2-related_cerebral_small_vessel_disease": 2,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Inborn_genetic_diseases": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "not_provided|Porencephalic_cyst|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity": 3,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "not_provided|Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 7,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 3,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|not_provided|not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Porencephalic_cyst|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 4,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided|not_specified": 1,
    "not_provided|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Congenital_anomaly_of_kidney_and_urinary_tract|Inborn_genetic_diseases": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 2,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 8,
    "not_provided|Porencephalic_cyst|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|COL4A1-related_disorder": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "COL4A1-related_disorder|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Retinal_arteries": 1,
    "not_specified|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "COL4A1-related_disorder|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 3,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|not_specified": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 2,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 17,
    "not_provided|Congenital_anomaly_of_kidney_and_urinary_tract|Retinal_arterial_tortuosity": 1,
    "not_provided|not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 2,
    "Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|not_specified": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "not_specified|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microcephaly": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_specified": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|not_specified": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 3,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 7,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_specified|COL4A1-related_disorder|Porencephalic_cyst": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided": 4,
    "not_provided|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 6,
    "Porencephaly": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 1,
    "Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|Inborn_genetic_diseases|COL4A1-related_disorder": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|not_provided": 1,
    "COL4A1-related_disorder|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 3,
    "not_provided|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|COL4A1-related_disorder": 1,
    "not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "COL4A1-related_disorder|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided": 1,
    "COL4A1-related_disorder|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "Inborn_genetic_diseases|not_provided|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|not_specified|not_provided": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|COL4A1-related_disorder|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|COL4A1-related_disorder": 1,
    "Inborn_genetic_diseases|COL4A1-related_disorder|not_provided": 2,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|not_provided": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Porencephalic_cyst|not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 6,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "COL4A1-related_disorder|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|COL4A1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|not_provided": 1,
    "not_provided|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Inborn_genetic_diseases|COL4A1-related_disorder": 1,
    "Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|HANAC-like_syndrome|not_provided": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|COL4A1-related_disorder": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|not_provided": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 4,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided": 2,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst": 2,
    "Developmental_cataract|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_specified|not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "Inborn_genetic_diseases|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_specified|not_provided": 1,
    "Cerebral_calcification|Intracranial_hemorrhage|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Abnormal_corpus_callosum_morphology|Intraventricular_hemorrhage": 1,
    "not_provided|Inborn_genetic_diseases|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity": 1,
    "Inborn_genetic_diseases|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder": 1,
    "COL4A1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 1,
    "Proteinuria|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_specified|not_provided": 1,
    "not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|not_provided|COL4A1-related_disorder": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst|not_specified|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|not_provided": 2,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|COL4A1-related_disorder|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Inborn_genetic_diseases": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "COL4A1-related_disorder|not_specified|not_provided": 1,
    "not_provided|COL4A1-related_disorder|Inborn_genetic_diseases": 1,
    "COL4A1_or_COL4A2-related_cerebral_small_vessel_disease|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|COL4A1-related_disorder|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|not_specified": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Schizencephaly|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Inborn_genetic_diseases|COL4A1-related_disorder|not_provided|Porencephalic_cyst": 1,
    "Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst": 1,
    "Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Microcephaly|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Inborn_genetic_diseases|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "COL4A1-related_disorder|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "not_provided|not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "not_specified|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Inborn_genetic_diseases|COL4A1-related_disorder": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|COL4A1-related_disorder|not_specified": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|not_provided": 1,
    "COL4A1-related_disorder|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "COL4A1-related_disorder|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|not_provided": 1,
    "Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|COL4A1-related_disorder|not_provided": 1,
    "Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|COL4A1-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|not_provided": 1,
    "not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|not_specified|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|not_provided|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "COL4A1-related_disorder|not_specified|not_provided|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided|not_specified|Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Anterior_segment_dysgenesis|not_provided": 1,
    "not_specified|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided|not_specified": 1,
    "not_provided|COL4A1-related_disorder|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided|not_specified": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|not_provided|not_specified|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity": 1,
    "COL4A1-related_disorder|Vascular_dementia|not_provided": 1,
    "Irido-corneo-trabecular_dysgenesis|not_provided": 1,
    "Colpocephaly|Abnormal_cerebral_cortex_morphology|Corpus_callosum|_agenesis_of|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Porencephalic_cyst|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|COL4A1-related_disorder": 1,
    "COL4A1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Retinal_arterial_tortuosity|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|not_provided|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided|COL4A1-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst": 1,
    "Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Inborn_genetic_diseases": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|not_provided": 1,
    "Porencephalic_cyst|not_specified|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "not_provided|Congenital_anomaly_of_kidney_and_urinary_tract|COL4A1-related_disorder|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|COL4A1-related_disorder|Optic_nerve_hypoplasia|not_specified|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Chronic_kidney_disease": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_specified|Porencephalic_cyst|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 2,
    "Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_specified": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Retinal_arterial_tortuosity": 1,
    "Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Microangiopathy_and_leukoencephalopathy|_pontine|_autosomal_dominant|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Hemorrhage|_intracerebral|_susceptibility_to|Retinal_arterial_tortuosity|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|COL4A1-related_disorder|Retinal_arterial_tortuosity|Hemorrhage|_intracerebral|_susceptibility_to|Schizencephaly|Inborn_genetic_diseases|not_provided": 1,
    "Porencephalic_cyst|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|not_provided": 1,
    "Porencephalic_cyst|Porencephaly_2|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|not_provided": 1,
    "Porencephaly_2": 92,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome|Porencephalic_cyst|not_provided|Porencephaly_2": 1,
    "Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Porencephalic_cyst|Porencephaly_2|not_provided|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 1,
    "Porencephalic_cyst|Porencephaly_2|not_provided|Brain_small_vessel_disease_1_with_or_without_ocular_anomalies|Autosomal_dominant_familial_hematuria-retinal_arteriolar_tortuosity-contractures_syndrome": 3,
    "not_provided|Porencephaly_2": 51,
    "COL4A2-related_disorder": 32,
    "not_provided|Porencephaly_2|Inborn_genetic_diseases": 5,
    "not_provided|COL4A2-related_disorder": 16,
    "Porencephaly_2|not_provided": 48,
    "not_provided|COL4A2-related_disorder|Inborn_genetic_diseases": 4,
    "not_provided|Porencephaly_2|Hemorrhage|_intracerebral|_susceptibility_to|not_specified": 2,
    "Porencephaly_2|COL4A2-related_disorder": 2,
    "Hemorrhage|_intracerebral|_susceptibility_to|Porencephaly_2|not_provided": 2,
    "COL4A2-related_disorder|not_provided": 20,
    "not_specified|not_provided|Inborn_genetic_diseases|Porencephaly_2": 1,
    "COL4A2-related_disorder|Porencephaly_2": 1,
    "not_provided|Inborn_genetic_diseases|Porencephaly_2": 4,
    "Porencephaly_2|COL4A2-related_cerebral_small_vessel_disease": 1,
    "Porencephaly_2|Encephalopathy|_progressive|_early-onset|_with_brain_edema_and/or_leukoencephalopathy|_1": 1,
    "not_provided|Porencephaly_2|not_specified": 1,
    "Joint_hypermobility": 1,
    "not_provided|COL4A2-related_disorder|Porencephaly_2": 13,
    "Porencephaly_2|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|not_specified": 1,
    "Porencephaly_2|not_provided|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "not_provided|not_specified|Porencephaly_2": 6,
    "Porencephalic_cyst": 3,
    "COL4A2-related_disorder|Porencephaly_2|not_provided": 3,
    "Porencephaly_2|not_provided|not_specified": 9,
    "Porencephaly_2|Inborn_genetic_diseases|not_provided": 3,
    "Porencephaly_2|not_provided|Inborn_genetic_diseases": 1,
    "Porencephaly_2|COL4A2-related_disorder|not_provided|concomitant_exotropia": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Porencephaly_2": 2,
    "not_provided|Inborn_genetic_diseases|COL4A2-related_disorder|Porencephaly_2": 1,
    "Inborn_genetic_diseases|Porencephaly_2|not_provided": 2,
    "COL4A2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|not_specified|Hemorrhage|_intracerebral|_susceptibility_to|Intellectual_disability": 1,
    "Porencephaly_2|COL4A2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "COL4A2-related_disorder|Inborn_genetic_diseases": 1,
    "COL4A2-related_disorder|not_provided|Porencephaly_2": 1,
    "Vasculitis": 1,
    "Optic_nerve_hypoplasia|COL4A2-related_disorder|not_provided|Porencephaly_2": 1,
    "See_cases|COL4A2-related_disorder|not_specified|not_provided": 1,
    "concomitant_exotropia|Inborn_genetic_diseases|not_provided": 1,
    "COL4A2-related_disorder|not_provided|See_cases|Optic_nerve_hypoplasia|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Porencephaly_2": 2,
    "Porencephalic_cyst|not_provided": 2,
    "Inborn_genetic_diseases|COL4A2-related_disorder|not_provided": 1,
    "Porencephaly_2|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 3,
    "Inborn_genetic_diseases|Porencephaly_2": 2,
    "COL4A2-related_disorder|not_specified|not_provided": 1,
    "Porencephaly_2|Hemorrhage|_intracerebral|_susceptibility_to": 2,
    "Porencephaly_2|not_specified|not_provided": 1,
    "Porencephaly_2|Inborn_genetic_diseases": 2,
    "Porencephaly_2|not_provided|Bethlem_myopathy_2": 1,
    "Porencephaly_2|not_specified": 2,
    "Inborn_genetic_diseases|COL4A2-related_disorder": 1,
    "COL4A2-related_disorder|Porencephaly_2|Hemorrhage|_intracerebral|_susceptibility_to|not_specified": 1,
    "not_specified|not_provided|Porencephaly_2|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "COL4A2-related_disorder|Hemorrhage|_intracerebral|_susceptibility_to|Porencephaly_2|not_provided": 2,
    "not_provided|Intellectual_disability|Cerebral_palsy|Seizure": 1,
    "COL4A2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|COL4A2-related_disorder|Inborn_genetic_diseases|Porencephaly_2": 1,
    "not_provided|Porencephaly_2|Cerebral_palsy": 1,
    "Porencephaly_2|Intraventricular_hemorrhage": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Inborn_genetic_diseases|Porencephaly_2|not_provided": 1,
    "not_provided|Porencephaly_2|concomitant_exotropia": 1,
    "not_provided|COL4A2-related_disorder|Porencephaly_2|concomitant_exotropia": 1,
    "COL4A2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "COL4A2-related_disorder|Porencephaly_2|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|COL4A2-related_disorder": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Porencephaly_2": 2,
    "COL4A2-related_disorder|Inborn_genetic_diseases|not_provided|Porencephaly_2": 1,
    "Optic_nerve_hypoplasia|not_specified|not_provided|Inborn_genetic_diseases|Porencephaly_2": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 1,
    "not_provided|Porencephalic_cyst": 1,
    "Intellectual_disability|Porencephaly_2": 1,
    "NAD(P)HX_dehydratase_deficiency": 19,
    "not_provided|NAXD-related_disorder": 8,
    "NAXD-related_disorder|not_provided": 6,
    "not_provided|NAD(P)HX_dehydratase_deficiency|NAXD-related_disorder": 1,
    "NAXD-related_disorder": 3,
    "not_provided|NAXD-related_disorder|NAD(P)HX_dehydratase_deficiency": 1,
    "not_provided|NAD(P)HX_dehydratase_deficiency": 1,
    "NAD(P)HX_dehydratase_deficiency|not_provided": 2,
    "NAD(P)HX_dehydratase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|NAD(P)HX_dehydratase_deficiency": 1,
    "NAD(P)HX_dehydratase_deficiency|NAXD-related_disorder|not_provided": 1,
    "See_cases|NAD(P)HX_dehydratase_deficiency|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_27": 526,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_27": 8,
    "CARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_27|not_provided": 1,
    "CARS2-related_disorder|not_provided|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_27|not_specified": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_27": 21,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_27|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_27|CARS2-related_disorder|not_specified": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|not_specified|not_provided": 5,
    "Combined_oxidative_phosphorylation_defect_type_27|not_provided": 15,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_27|not_provided": 7,
    "Combined_oxidative_phosphorylation_defect_type_27|not_specified": 14,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_27": 26,
    "Combined_oxidative_phosphorylation_defect_type_27|Inborn_genetic_diseases|not_provided": 2,
    "Combined_oxidative_phosphorylation_defect_type_27|Inborn_genetic_diseases": 19,
    "Combined_oxidative_phosphorylation_defect_type_27|CARS2-related_disorder": 4,
    "not_provided|CARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|CARS2-related_disorder|not_provided": 3,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_27|not_provided": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_27|CARS2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|not_provided|Inborn_genetic_diseases": 4,
    "Combined_oxidative_phosphorylation_defect_type_27|not_provided|not_specified": 5,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|not_provided|CARS2-related_disorder": 2,
    "CARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_27": 2,
    "not_provided|not_specified|CARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|CARS2-related_disorder|not_specified": 1,
    "See_cases|Combined_oxidative_phosphorylation_defect_type_27": 2,
    "CARS2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|Maturity-onset_diabetes_of_the_young_type_2": 1,
    "CARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_27|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_27": 1,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_27": 2,
    "Inborn_genetic_diseases|CARS2-related_disorder|Combined_oxidative_phosphorylation_defect_type_27|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_27|not_provided|CARS2-related_disorder|Inborn_genetic_diseases": 1,
    "SOX1-related_disorder": 8,
    "SOX1-related_disorder|not_specified": 1,
    "Hearing_loss|_autosomal_dominant_84": 4,
    "Leukodystrophy|_hypomyelinating|_24": 2,
    "ATP11A-related_disorder": 9,
    "Inborn_genetic_diseases|ATP11A-related_disorder": 3,
    "not_provided|ATP11A-related_disorder": 2,
    "ATP11A-related_disorder|not_provided": 3,
    "ATP11A-related_disorder|Inborn_genetic_diseases": 1,
    "Hearing_loss|_autosomal_dominant_84|Autosomal_dominant_nonsyndromic_hearing_loss_33": 1,
    "Auditory_neuropathy|_autosomal_dominant_2": 1,
    "ATP11A-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Myocardial_infarction|_decreased_susceptibility_to": 1,
    "Hemophilia": 1,
    "Factor_VII_deficiency": 78,
    "Congenital_factor_VII_deficiency|Factor_VII_deficiency": 5,
    "Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to": 4,
    "F7-related_disorder": 17,
    "Congenital_factor_VII_deficiency|Factor_VII_deficiency|not_provided": 3,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency": 2,
    "Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|not_specified|Factor_VII_deficiency": 1,
    "not_provided|Factor_VII_deficiency": 4,
    "not_provided|not_specified|Factor_VII_deficiency": 2,
    "not_provided|Congenital_factor_VII_deficiency": 4,
    "Factor_VII_deficiency|not_provided": 5,
    "Congenital_factor_VII_deficiency": 32,
    "not_specified|Congenital_factor_VII_deficiency": 2,
    "Inborn_genetic_diseases|Congenital_factor_VII_deficiency": 3,
    "Factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|F7-related_disorder": 1,
    "F7-related_disorder|Congenital_factor_VII_deficiency": 2,
    "Congenital_factor_VII_deficiency|not_provided|not_specified": 1,
    "Factor_VII_deficiency|Congenital_factor_VII_deficiency|not_provided": 2,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|not_provided": 1,
    "not_provided|not_specified|Congenital_factor_VII_deficiency": 1,
    "Congenital_factor_VII_deficiency|Factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|not_provided": 1,
    "Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|not_specified": 1,
    "Factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|not_provided|F7-related_disorder": 2,
    "Factor_VII_deficiency|not_specified": 1,
    "not_specified|F7-related_disorder|not_provided": 1,
    "not_provided|Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to": 2,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|not_provided|See_cases": 1,
    "not_specified|Abnormal_bleeding": 2,
    "not_provided|Congenital_factor_VII_deficiency|F7-related_disorder": 1,
    "not_provided|Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|not_specified": 1,
    "Congenital_factor_VII_deficiency|not_provided|Factor_VII_deficiency": 2,
    "Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|Factor_VII_deficiency|F7-related_disorder|not_provided": 1,
    "not_provided|Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency": 1,
    "not_specified|not_provided|Factor_VII_deficiency": 1,
    "not_provided|Factor_VII_deficiency|not_specified": 1,
    "Congenital_factor_VII_deficiency|not_provided|Abnormality_of_coagulation|F7-related_disorder": 1,
    "Congenital_factor_VII_deficiency|Factor_VII_deficiency|F7-related_disorder|not_provided": 1,
    "F7-related_disorder|Factor_VII_deficiency": 1,
    "not_provided|Factor_VII_deficiency|F7-related_disorder|Congenital_factor_VII_deficiency": 1,
    "Congenital_factor_VII_deficiency|F7-related_disorder": 1,
    "not_specified|Factor_VII_deficiency": 2,
    "Factor_VII_deficiency|Congenital_factor_VII_deficiency": 1,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|F7-related_disorder|not_provided|Factor_VII_deficiency|Abnormal_bleeding": 1,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|F7-related_disorder": 1,
    "not_provided|Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|F7-related_disorder|Factor_VII_Padua|Factor_VII_deficiency": 1,
    "Congenital_factor_VII_deficiency|Factor_VII_deficiency|See_cases|Myocardial_infarction|_susceptibility_to|not_provided": 1,
    "not_provided|F7-related_disorder": 1,
    "Congenital_factor_VII_deficiency|Inborn_genetic_diseases": 1,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|not_provided|Factor_VII_deficiency|F7-related_disorder": 1,
    "Congenital_factor_VII_deficiency|not_specified": 1,
    "Abnormal_bleeding|Abnormality_of_coagulation": 1,
    "Congenital_factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|Factor_VII_deficiency": 1,
    "not_specified|not_provided|Myocardial_infarction|_decreased_susceptibility_to|Factor_VII_deficiency|Factor_X_deficiency": 1,
    "Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|Factor_VII_deficiency|F7-related_disorder": 1,
    "Factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|F7-related_disorder|not_provided": 1,
    "Factor_VII_deficiency|Myocardial_infarction|_susceptibility_to|Congenital_factor_VII_deficiency|not_provided|Abnormal_bleeding|F7-related_disorder": 1,
    "Factor_VII_deficiency|Factor_X_deficiency|not_provided": 8,
    "Factor_VII_deficiency|Factor_X_deficiency": 3,
    "Hereditary_factor_X_deficiency_disease": 43,
    "Factor_X_deficiency": 19,
    "not_provided|Hereditary_factor_X_deficiency_disease": 10,
    "not_provided|Factor_X_deficiency": 2,
    "F10-related_disorder": 3,
    "Hereditary_factor_X_deficiency_disease|Inborn_genetic_diseases": 2,
    "Hereditary_factor_X_deficiency_disease|Factor_X_deficiency": 1,
    "Hereditary_factor_X_deficiency_disease|Factor_X_deficiency|F10-related_disorder": 1,
    "not_provided|F10-related_disorder": 1,
    "Hereditary_factor_X_deficiency_disease|not_specified|not_provided": 2,
    "not_provided|Hereditary_factor_X_deficiency_disease|F10-related_disorder": 2,
    "F10-related_disorder|Hereditary_factor_X_deficiency_disease|not_specified|not_provided|Factor_X_deficiency|Abnormal_bleeding": 1,
    "Hereditary_factor_X_deficiency_disease|not_provided": 4,
    "Hereditary_factor_X_deficiency_disease|F10-related_disorder": 1,
    "Factor_x_deficiency|_autosomal_dominant": 1,
    "not_provided|Hereditary_factor_X_deficiency_disease|Factor_X_deficiency": 1,
    "F10-related_disorder|Hereditary_factor_X_deficiency_disease|Factor_X_deficiency": 1,
    "Inborn_genetic_diseases|F10-related_disorder": 1,
    "not_specified|Hereditary_factor_X_deficiency_disease": 1,
    "Abnormal_bleeding|Thrombocytopenia|Factor_X_deficiency|Hereditary_factor_X_deficiency_disease": 1,
    "Thrombocytopenia|Abnormal_bleeding|Hereditary_factor_X_deficiency_disease": 1,
    "Protein_Z_deficiency": 4,
    "PROZ-related_disorder": 3,
    "Protein_Z_deficiency|not_provided": 1,
    "PROZ-related_disorder|not_provided": 1,
    "Retinal_dystrophy|Oguchi_disease-2": 2,
    "not_provided|GRK1-related_disorder|Oguchi_disease-2|not_specified": 1,
    "GRK1-related_disorder": 9,
    "Retinal_dystrophy|not_provided|Oguchi_disease-2": 1,
    "Congenital_stationary_night_blindness|Oguchi_disease-2": 1,
    "Retinal_dystrophy|Oguchi_disease-2|not_provided": 1,
    "CHAMP1-related_disorder": 18,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder|CHAMP1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_40": 43,
    "not_provided|CHAMP1-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|CHAMP1-related_disorder|not_provided": 1,
    "CHAMP1-related_disorder|not_provided": 7,
    "not_provided|Intellectual_disability|_autosomal_dominant_40|CHAMP1-related_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_40|intellectual_disability_with_severe_speech_impairment": 3,
    "CHAMP1-related_syndrome|Intellectual_disability|_autosomal_dominant_40": 1,
    "not_provided|CHAMP1-related_disorder": 7,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_40": 1,
    "CHAMP1-related_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|CHAMP1-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_40|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_40|CHAMP1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_40|CHAMP1-related_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_40|intellectual_disability_with_severe_speech_impairment|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_40|Inborn_genetic_diseases|Complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|CHAMP1-related_disorder": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_40|CHAMP1-related_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|CHAMP1-related_syndrome": 4,
    "CHAMP1-related_syndrome": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_40": 1,
    "CHAMP1-related_disorder|CHAMP1-related_syndrome": 1,
    "Neurodevelopmental_disorder_with_cerebral_atrophy_and_variable_facial_dysmorphism|not_provided": 1,
    "Neurodevelopmental_delay|Neurodevelopmental_disorder_with_cerebral_atrophy_and_variable_facial_dysmorphism": 1,
    "Neurodevelopmental_disorder_with_cerebral_atrophy_and_variable_facial_dysmorphism": 13,
    "TTC5-related_disorder": 1,
    "TEP1-related_condition": 1,
    "Galloway-Mowat_syndrome|Galloway-Mowat_syndrome_3|not_provided": 1,
    "Galloway-Mowat_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "OSGEP-related_disorder": 5,
    "Galloway-Mowat_syndrome_3|Radioulnar_synostosis_with_amegakaryocytic_thrombocytopenia_2": 1,
    "Galloway-Mowat_syndrome_3": 13,
    "Inborn_genetic_diseases|Galloway-Mowat_syndrome_3": 2,
    "Inborn_genetic_diseases|not_provided|Galloway-Mowat_syndrome_3": 1,
    "Galloway-Mowat_syndrome_3|not_provided": 5,
    "Inborn_genetic_diseases|Nephrotic_syndrome|not_provided|Galloway-Mowat_syndrome_3": 1,
    "not_provided|Inborn_genetic_diseases|OSGEP-related_disorder": 1,
    "OSGEP-related_disorder|not_provided": 1,
    "not_provided|Galloway-Mowat_syndrome_3": 4,
    "not_provided|OSGEP-related_disorder": 3,
    "See_cases|not_provided|OSGEP-related_disorder|Galloway-Mowat_syndrome_3": 1,
    "OSGEP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Galloway-Mowat_syndrome_3|Nephrotic_syndrome|not_provided": 1,
    "APEX1-related_disorder|not_provided": 2,
    "not_provided|APEX1-related_disorder": 2,
    "Purine-nucleoside_phosphorylase_deficiency": 218,
    "not_provided|Purine-nucleoside_phosphorylase_deficiency": 9,
    "not_specified|not_provided|Purine-nucleoside_phosphorylase_deficiency": 4,
    "Purine-nucleoside_phosphorylase_deficiency|not_specified": 3,
    "not_specified|not_provided|PNP_POLYMORPHISM|Purine-nucleoside_phosphorylase_deficiency": 1,
    "Purine-nucleoside_phosphorylase_deficiency|not_provided": 8,
    "Purine-nucleoside_phosphorylase_deficiency|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Purine-nucleoside_phosphorylase_deficiency|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Purine-nucleoside_phosphorylase_deficiency": 2,
    "Severe_combined_immunodeficiency_disease|Purine-nucleoside_phosphorylase_deficiency": 2,
    "Purine-nucleoside_phosphorylase_deficiency|Severe_combined_immunodeficiency_disease": 2,
    "PNP-related_disorder|not_provided|not_specified|Purine-nucleoside_phosphorylase_deficiency": 1,
    "not_specified|Purine-nucleoside_phosphorylase_deficiency": 1,
    "not_provided|not_specified|Purine-nucleoside_phosphorylase_deficiency": 1,
    "Purine-nucleoside_phosphorylase_deficiency|not_specified|PNP-related_disorder": 1,
    "Severe_combined_immunodeficiency_disease|not_provided|Purine-nucleoside_phosphorylase_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|Purine-nucleoside_phosphorylase_deficiency|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_9": 23,
    "not_provided|Amyotrophic_lateral_sclerosis_type_9": 9,
    "ANG-related_disorder": 4,
    "not_provided|Amyotrophic_lateral_sclerosis_type_9|Amyotrophic_lateral_sclerosis_type_10|ANG-related_disorder": 1,
    "ANG-related_disorder|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_9|not_provided": 4,
    "Amyotrophic_lateral_sclerosis_type_9|Inborn_genetic_diseases|not_provided": 1,
    "ANG-related_disorder|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_9": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_9|not_provided|ANG-related_disorder": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_9|ANG-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_9|not_specified|not_provided": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_9|not_provided": 1,
    "Inborn_genetic_diseases|ANG-related_disorder|not_provided|Frontotemporal_dementia": 1,
    "not_provided|ANG-related_disorder|Amyotrophic_lateral_sclerosis_type_9": 1,
    "ARHGEF40_related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_74|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_74": 2,
    "HNRNPC-related_condition": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 446,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Inborn_genetic_diseases": 19,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 221,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided": 9,
    "not_provided|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 9,
    "Leber_congenital_amaurosis_6": 26,
    "Retinal_dystrophy|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 16,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided": 1,
    "Cone-rod_dystrophy_13": 7,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_6": 2,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Retinal_dystrophy": 2,
    "not_specified|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided": 5,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided|Cone_dystrophy|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_6|not_provided|not_specified|Cone-rod_dystrophy_13": 2,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 10,
    "Retinal_dystrophy|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 3,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|RPGRIP1-related_disorder": 2,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Inborn_genetic_diseases": 12,
    "not_provided|not_specified|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 2,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_specified|not_provided|RPGRIP1-related_disorder": 1,
    "Leber_congenital_amaurosis_6|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_specified": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_specified|Inborn_genetic_diseases|RPGRIP1-related_disorder": 1,
    "Leber_congenital_amaurosis|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 2,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Retinal_dystrophy": 4,
    "not_specified|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 2,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 13,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|RPGRIP1-related_disorder|not_provided|not_specified|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 4,
    "Cone-rod_dystrophy|not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 1,
    "not_provided|not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "RPGRIP1-related_disorder|not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_specified": 4,
    "Cone-rod_dystrophy_13|Inborn_genetic_diseases|Leber_congenital_amaurosis_6|not_provided": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Inborn_genetic_diseases": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided|Leber_congenital_amaurosis": 2,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 3,
    "Retinal_dystrophy|Leber_congenital_amaurosis_6": 1,
    "not_provided|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Leber_congenital_amaurosis": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_6": 1,
    "not_provided|Cone-rod_dystrophy|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_6|Cone-rod_dystrophy|Retinal_dystrophy|Cone-rod_dystrophy_13": 1,
    "not_provided|not_specified|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_1|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_specified|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided": 2,
    "RPGRIP1-related_disorder|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 2,
    "not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Retinal_dystrophy|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_6|Leber_congenital_amaurosis|RPGRIP1-related_disorder|Cone-rod_dystrophy_13": 1,
    "not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Leber_congenital_amaurosis_1|not_provided": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 2,
    "Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 2,
    "not_provided|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_specified": 2,
    "not_provided|Leber_congenital_amaurosis_6": 3,
    "Retinal_dystrophy|RPGRIP1-related_disorder|not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|RPGRIP1-related_disorder|not_provided": 2,
    "RPGRIP1-related_disorder|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 1,
    "RPGRIP1-related_disorder": 3,
    "Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_6|Retinal_dystrophy|Cone-rod_dystrophy_13|RPGRIP1-related_disorder": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_provided": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_specified": 3,
    "Abnormality_of_the_eye|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Leber_congenital_amaurosis": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_1": 1,
    "not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Leber_congenital_amaurosis": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Retinal_dystrophy|Leber_congenital_amaurosis": 1,
    "Cone-rod_dystrophy_13|Retinal_dystrophy|not_provided": 1,
    "not_specified|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 1,
    "Retinal_dystrophy|Optic_atrophy|not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 1,
    "Retinal_dystrophy|Horizontal_nystagmus|Color_vision_defect|Visual_impairment|Leber_congenital_amaurosis_6": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "not_provided|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_6|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_13": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_6|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Leber_congenital_amaurosis|Leber_congenital_amaurosis_1": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided|not_specified": 1,
    "Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|not_specified|not_provided": 2,
    "Joubert_syndrome_7": 11,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13|Inborn_genetic_diseases": 1,
    "Microcephaly|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6": 1,
    "Leber_congenital_amaurosis_6|Retinal_dystrophy|Cone-rod_dystrophy_13": 1,
    "Cone-rod_dystrophy_13|Leber_congenital_amaurosis_6|not_provided|Retinitis_pigmentosa": 1,
    "Cone-Rod_Dystrophy|_Recessive|Leber_congenital_amaurosis|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 1,
    "Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis_6|Cone-rod_dystrophy_13": 1,
    "not_provided|SUPT16H-related_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_thin_corpus_callosum": 23,
    "SUPT16H-related_disorder": 14,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_thin_corpus_callosum|Inborn_genetic_diseases": 1,
    "SUPT16H-related_disorder|not_provided": 2,
    "Li-Fraumeni_syndrome_1": 193,
    "Dextrocardia|Conotruncal_defect": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly": 127,
    "not_provided|CHD8-related_disorder": 10,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided": 13,
    "not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly": 22,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided": 3,
    "not_provided|Intellectual_disability|CHD8-related_disorder": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly|Neurodevelopmental_disorder|CHD8-related_disorder": 1,
    "CHD8-related_disorder": 16,
    "CHD8-related_disorder|not_provided": 8,
    "not_specified|Intellectual_developmental_disorder_with_autism_and_macrocephaly|Neurodevelopmental_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|Inborn_genetic_diseases": 4,
    "CHD8-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "CHD8-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|CHD8-related_disorder": 3,
    "not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly|Inborn_genetic_diseases": 3,
    "not_provided|CHD8-related_disorder|Inborn_genetic_diseases|not_specified": 2,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|Inborn_genetic_diseases|not_specified|CHD8-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CHD8-related_disorder": 5,
    "Inborn_genetic_diseases|CHD8-related_disorder": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly": 2,
    "not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly|Intellectual_disability": 1,
    "Inborn_genetic_diseases|CHD8-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Complex_neurodevelopmental_disorder|not_provided": 1,
    "Intellectual_disability|Intellectual_developmental_disorder_with_autism_and_macrocephaly": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly|CHD8-related_disorder": 2,
    "Macrocephaly": 1,
    "not_provided|Intellectual_developmental_disorder_with_autism_and_macrocephaly|Inborn_genetic_diseases|CHD8-related_disorder": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|CHD8-related_disorder|Intellectual_developmental_disorder_with_autism_and_macrocephaly|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autism_and_macrocephaly": 2,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided|Autism_spectrum_disorder": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided|CHD8-related_disorder": 1,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided|Neurodevelopmental_disorder": 1,
    "not_provided|Autism_spectrum_disorder|Intellectual_developmental_disorder_with_autism_and_macrocephaly": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autism_and_macrocephaly": 3,
    "Intellectual_developmental_disorder_with_autism_and_macrocephaly|not_provided|Autism_spectrum_disorder|CHD8-related_disorder": 1,
    "Intellectual_disability|Autism_spectrum_disorder": 2,
    "Intellectual_disability|CHD8-related_disorder": 1,
    "not_provided|CHD8-related_disorder|Inborn_genetic_diseases": 4,
    "Developmental_delay|Motor_delay|Delayed_speech_and_language_development|Tall_stature": 1,
    "not_provided|Congenital_ptosis|Overgrowth|Fatigable_weakness|Increased_muscle_fatiguability|Macrocephaly": 1,
    "CHD8-associated_Neurodevelopmental_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|CHD8-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Autism": 1,
    "Inborn_genetic_diseases|not_provided|Complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|CHD8-related_disorder": 1,
    "SALL2-related_disorder": 9,
    "Coloboma|_ocular|_autosomal_recessive": 4,
    "not_provided|SALL2-related_disorder": 3,
    "SALL2-related_disorder|not_provided": 4,
    "TCR-alpha-beta-positive_T-cell_deficiency": 1,
    "OXA1L-related_disorder": 4,
    "Lysinuric_protein_intolerance": 666,
    "not_provided|Autoinflammatory_syndrome|Lysinuric_protein_intolerance": 1,
    "Lysinuric_protein_intolerance|not_provided|not_specified": 2,
    "Lysinuric_protein_intolerance|Inborn_genetic_diseases": 9,
    "Lysinuric_protein_intolerance|not_specified": 9,
    "SLC7A7-related_disorder|Lysinuric_protein_intolerance": 2,
    "Lysinuric_protein_intolerance|SLC7A7-related_disorder": 2,
    "not_specified|not_provided|Lysinuric_protein_intolerance": 2,
    "not_specified|Lysinuric_protein_intolerance": 13,
    "not_provided|Lysinuric_protein_intolerance": 9,
    "Inborn_genetic_diseases|Lysinuric_protein_intolerance": 16,
    "Inborn_genetic_diseases|SLC7A7-related_disorder|Lysinuric_protein_intolerance": 1,
    "Lysinuric_protein_intolerance|not_provided|Inborn_genetic_diseases": 3,
    "Autoinflammatory_syndrome|not_specified|not_provided|Lysinuric_protein_intolerance|SLC7A7-related_disorder": 1,
    "SLC7A7-related_disorder": 6,
    "Inborn_genetic_diseases|not_provided|Lysinuric_protein_intolerance": 2,
    "Autoinflammatory_syndrome|Lysinuric_protein_intolerance": 1,
    "Lysinuric_protein_intolerance|Autoinflammatory_syndrome": 1,
    "not_provided|not_specified|Lysinuric_protein_intolerance": 2,
    "Lysinuric_protein_intolerance|not_specified|Autoinflammatory_syndrome": 2,
    "Lysinuric_protein_intolerance|SLC7A7-related_disorder|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Lysinuric_protein_intolerance|not_provided": 1,
    "SLC7A7-related_disorder|Inborn_genetic_diseases|Lysinuric_protein_intolerance": 1,
    "Lysinuric_protein_intolerance|not_provided|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_provided|Lysinuric_protein_intolerance": 2,
    "Lysinuric_protein_intolerance|not_specified|not_provided": 2,
    "SLC7A7-related_disorder|not_provided|Lysinuric_protein_intolerance": 1,
    "SLC7A7-related_disorder|Lysinuric_protein_intolerance|Autoinflammatory_syndrome": 1,
    "Lysinuric_protein_intolerance|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Autoinflammatory_syndrome|not_provided|Inborn_genetic_diseases|Lysinuric_protein_intolerance": 1,
    "Lysinuric_protein_intolerance|not_specified|not_provided|Autoinflammatory_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Lysinuric_protein_intolerance": 1,
    "Autoinflammatory_syndrome|not_provided|not_specified|Lysinuric_protein_intolerance": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Lysinuric_protein_intolerance": 1,
    "Inborn_genetic_diseases|Lysinuric_protein_intolerance|not_provided": 1,
    "not_specified|Lysinuric_protein_intolerance|SLC7A7-related_disorder|not_provided": 1,
    "MMP14-related_disorder|not_provided": 3,
    "Winchester_syndrome": 4,
    "not_provided|MMP14-related_disorder": 2,
    "Winchester_syndrome|not_provided": 1,
    "MMP14-related_disorder": 1,
    "not_provided|LRP10-related_disorder": 4,
    "LRP10-related_disorder": 7,
    "LRP10-related_disorder|not_specified": 1,
    "CIROP-related_disorder": 1,
    "Heterotaxy|_visceral|_12|_autosomal": 9,
    "CIROP-related_disorder|Heterotaxy|_visceral|_12|_autosomal": 1,
    "Specific_granule_deficiency_1|Specific_granule_deficiency|CEBPE-related_disorder": 1,
    "CEBPE-related_disorder|not_provided|Specific_granule_deficiency": 1,
    "Specific_granule_deficiency": 147,
    "Specific_granule_deficiency_1": 5,
    "Specific_granule_deficiency|not_provided|CEBPE-related_disorder": 1,
    "CEBPE-related_disorder|Specific_granule_deficiency": 3,
    "Pelger-Huet-like_anomaly_and_episodic_fever_with_abdominal_pain": 1,
    "Specific_granule_deficiency_1|SPECIFIC_GRANULE_DEFICIENCY_1|_AUTOSOMAL_DOMINANT": 1,
    "Specific_granule_deficiency|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Specific_granule_deficiency": 7,
    "not_provided|Specific_granule_deficiency": 4,
    "Specific_granule_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Specific_granule_deficiency|not_provided": 4,
    "Specific_granule_deficiency|not_specified": 2,
    "CEBPE-related_disorder|Specific_granule_deficiency|not_provided": 1,
    "Specific_granule_deficiency|Specific_granule_deficiency_1": 1,
    "not_provided|Inborn_genetic_diseases|Specific_granule_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Specific_granule_deficiency": 1,
    "CEBPE-related_disorder": 2,
    "CEBPE-related_disorder|Specific_granule_deficiency|not_provided|Specific_granule_deficiency_1": 1,
    "Specific_granule_deficiency|CEBPE-related_disorder": 1,
    "CEBPE-related_disorder|not_specified": 1,
    "not_provided|Oculopharyngeal_muscular_dystrophy_1|PABPN1-related_disorder": 1,
    "not_provided|not_specified|Oculopharyngeal_muscular_dystrophy_1": 1,
    "Oculopharyngeal_muscular_dystrophy_1|Inborn_genetic_diseases|not_provided|Oculopharyngeal_muscular_dystrophy": 1,
    "Oculopharyngeal_muscular_dystrophy_1|not_provided|Oculopharyngeal_muscular_dystrophy": 2,
    "not_provided|Oculopharyngeal_muscular_dystrophy": 1,
    "not_provided|Oculopharyngeal_muscular_dystrophy_1": 2,
    "Oculopharyngeal_muscular_dystrophy_1|not_provided": 2,
    "PABPN1-related_disorder|Oculopharyngeal_muscular_dystrophy_1": 1,
    "Inborn_genetic_diseases|Oculopharyngeal_muscular_dystrophy_1": 1,
    "Oculopharyngeal_muscular_dystrophy": 1,
    "not_provided|PABPN1-related_disorder|not_specified": 1,
    "PABPN1-related_disorder|not_provided": 1,
    "not_provided|BCL2L2-PABPN1-related_disorder": 1,
    "PABPN1-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14": 26,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 141,
    "not_provided|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14": 37,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 2,
    "Hypertrophic_cardiomyopathy_14|AV_Block_Third_Degree_Adverse_Event": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 158,
    "MYH6-related_disorder|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype": 3,
    "not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 28,
    "Hypertrophic_cardiomyopathy_14|not_specified|Cardiovascular_phenotype": 5,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|MYH6-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided|Cardiovascular_phenotype": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Congenital_heart_disease": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 25,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_14|not_specified": 13,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|MYH6-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|not_specified": 7,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_specified|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_14|not_provided": 7,
    "Cardiovascular_phenotype|MYH6-related_disorder|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE": 1,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 5,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|not_specified|Cardiovascular_phenotype": 2,
    "MYH6-related_disorder|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3": 2,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype": 26,
    "Hypertrophic_cardiomyopathy_14|not_provided": 30,
    "not_specified|Hypertrophic_cardiomyopathy_14": 24,
    "Atrial_septal_defect_3": 7,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 2,
    "not_provided|Atrial_septal_defect_3": 2,
    "not_specified|Cardiovascular_phenotype|Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 3,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|not_provided|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_specified": 10,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiomyopathy|Conduction_disorder_of_the_heart|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy|MYH6-related_disorder|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3": 2,
    "Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|not_provided|not_specified|Cardiovascular_phenotype|MYH6-related_disorder": 1,
    "Atrial_septal_defect_3|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Cardiomyopathy": 3,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Cardiomyopathy|MYH6-related_disorder|Cardiovascular_phenotype": 1,
    "MYH6-related_disorder|not_provided": 2,
    "not_provided|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 2,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 2,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_14": 2,
    "MYH6-related_disorder": 17,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 2,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_14": 3,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1A|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_14": 5,
    "not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 1,
    "Cardiovascular_phenotype|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3": 1,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Cardiovascular_phenotype|not_specified|MYH6-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_14": 11,
    "Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "not_specified|not_provided|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy|Chest_pain|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 10,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_provided": 17,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 2,
    "not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|MYH6-related_disorder": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|MYH6-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_provided|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 2,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided": 11,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|Cardiovascular_phenotype": 5,
    "not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Hypertrophic_cardiomyopathy_14|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|not_provided": 8,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_specified|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14": 7,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 6,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 2,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_provided": 4,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14": 4,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|MYH6-related_disorder|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_specified|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_specified": 9,
    "not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_specified": 3,
    "not_specified|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Cardiac_arrest": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1": 2,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14|not_specified": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_specified|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Migraine|Hemiplegia|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_specified|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|not_specified|MYH6-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|MYH6-related_disorder|Cardiovascular_phenotype": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_14|Wolff-Parkinson-White_pattern": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 2,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Cardiovascular_phenotype": 2,
    "not_provided|MYH6-related_disorder|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Cardiomyopathy": 1,
    "not_specified|MYH6-related_disorder|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|not_specified": 2,
    "not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 1,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 3,
    "not_provided|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_provided|not_specified": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_specified": 1,
    "Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14": 2,
    "MYH6-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Long_QT_syndrome|not_provided|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYH6-related_disorder|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_14|Cardiomyopathy|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 3,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1": 2,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 2,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|MYH6-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "Cardiovascular_phenotype|MYH6-related_disorder|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_specified|not_provided": 1,
    "not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 2,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "not_specified|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype|Congestive_heart_failure|not_provided": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|MYH6-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Atrial_septal_defect|Hypertrophic_cardiomyopathy_14|Cardiomyopathy|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiomyopathy|Atrial_septal_defect|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|not_specified|MYH6-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|not_specified|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Atrial_septal_defect|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_2|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Cardiomyopathy|not_specified": 1,
    "MYH6-related_disorder|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|MYH6-related_disorder|not_specified|Cardiomyopathy": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_14": 4,
    "not_specified|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_specified|not_provided": 1,
    "MYH6-related_cardiac_defects|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE": 2,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiomyopathy|not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|MYH6-related_disorder": 2,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided|Long_QT_syndrome|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype": 1,
    "not_provided|MYH6-related_disorder|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 3,
    "Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|MYH6-related_disorder|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|not_specified": 1,
    "not_specified|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Arrhythmogenic_right_ventricular_dysplasia_9|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Atrial_septal_defect|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_provided|not_specified": 1,
    "Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_provided|not_specified": 2,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1EE": 5,
    "Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Left_ventricular_noncompaction|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Left_ventricular_noncompaction|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|not_provided|Cardiomyopathy|MYH6-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|MYH6-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14": 2,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Migraine|Hemiplegia|Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|not_provided|Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_specified": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|not_specified": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_specified|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_provided": 2,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 2,
    "not_specified|Cardiovascular_phenotype|not_provided|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided": 1,
    "not_provided|MYH6-related_disorder|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 2,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH6-related_disorder": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_specified|not_provided": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Cardiomyopathy|not_specified|MYH6-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_provided|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE": 1,
    "MYH6-related_cardiac_defects|Cardiovascular_phenotype|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Ventricular_fibrillation|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype": 1,
    "Heart_disease|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|not_specified|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|MYH6-related_disorder": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "MYH6-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|Dilated_cardiomyopathy_1A|not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "not_provided|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYH6-related_disorder|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|not_specified|MYH6-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1": 1,
    "Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|not_specified|not_provided": 1,
    "not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided": 14,
    "Hypertrophic_cardiomyopathy_14|not_specified|Atrial_septal_defect_3|not_provided|Cardiovascular_phenotype": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "MYH6-related_disorder|not_provided|Heart|_malformation_of": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3": 1,
    "Cardiovascular_phenotype|not_provided|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|Conduction_system_disorder|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|MYH6-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|not_provided": 2,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Atrial_septal_defect|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|not_specified|not_provided|Cardiomyopathy": 1,
    "Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_specified|MYH6-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 2,
    "Cardiovascular_phenotype|MYH6-related_disorder|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|not_specified|not_provided": 1,
    "MYH6-related_disorder|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Atrial_septal_defect_3|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiomyopathy|not_provided|not_specified": 1,
    "MYH6-related_disorder|not_specified": 1,
    "Heart|_malformation_of|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3": 1,
    "not_specified|MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Cardiomyopathy|not_specified": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_14": 1,
    "Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_cardiac_defects|Atrial_septal_defect_3|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "MYH6-related_disorder|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|MYH6-related_disorder|not_provided|not_specified": 1,
    "Cardiomyopathy|not_provided|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|not_specified": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|not_provided": 1,
    "MYH6-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "MYH-6_related_congenital_heart_defects": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|MYH6-related_cardiac_defects|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Atrial_septal_defect|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_14|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|not_specified|not_provided": 2,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Brugada_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Long_QT_syndrome|Hypertrophic_cardiomyopathy_14": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_14|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_provided": 1,
    "Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14": 1,
    "Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 1,
    "MYH6-related_disorder|Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_14|not_specified|MYH6-related_disorder|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Atrial_septal_defect|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder": 1,
    "not_provided|Heart_failure|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_provided": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|not_specified": 1,
    "not_provided|MYH6-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|not_specified|MYH6-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|not_provided": 1,
    "not_provided|not_specified|MYH6-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_14": 1,
    "not_specified|Hypertrophic_cardiomyopathy_14|MYH6-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Dilated_cardiomyopathy_1EE|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Atrial_septal_defect|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|not_provided|MYH6-related_disorder|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Atrial_septal_defect_3|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3": 1,
    "Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Dilated_cardiomyopathy_1EE|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Hypertrophic_cardiomyopathy_1|Sick_sinus_syndrome_3|_susceptibility_to": 1,
    "Hypertrophic_cardiomyopathy_14|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Atrial_septal_defect_3|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_14|Cardiovascular_phenotype|Atrial_septal_defect_3|Dilated_cardiomyopathy_1EE|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_14": 1,
    "Dilated_cardiomyopathy_1EE|Hypertrophic_cardiomyopathy_14|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|Atrial_septal_defect_3|Sick_sinus_syndrome_3|_susceptibility_to|Hypertrophic_cardiomyopathy_14|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1EE": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified": 1,
    "not_specified|MYH6-related_disorder": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Hypertrophic_cardiomyopathy|Atrial_septal_defect|not_specified|Myosin_storage_myopathy|Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy": 1,
    "Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Hypertrophic_cardiomyopathy|Atrial_septal_defect|not_specified|Myosin_storage_myopathy|Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Scapuloperoneal_myopathy|not_specified|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 2,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy": 9,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Myosin_storage_myopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_4|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Left_ventricular_noncompaction_5": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Hypotonia": 1,
    "Myosin_storage_myopathy": 15,
    "MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_provided|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|Cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Dilated_cardiomyopathy_1S": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|Left_ventricular_noncompaction|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|MYH7-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy": 1,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Congenital_myopathy": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|not_provided|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_provided": 5,
    "Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_provided|MYH7-related_skeletal_myopathy": 2,
    "MYH7-related_disorder|not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 3,
    "Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|MYH7-related_disorder|Cardiomyopathy|not_provided|not_specified": 1,
    "MYH7-related_disorder|not_provided|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYH7-related_disorder|not_specified": 1,
    "Cardiomyopathy|Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Left_ventricular_noncompaction_1|Dilated_cardiomyopathy_1S|Hyaline_body_myopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiomyopathy|MYH7-related_skeletal_myopathy|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|MYH7-related_disorder": 3,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|MYH7-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy": 1,
    "Cardiovascular_phenotype|Prolonged_QT_interval|not_specified|Hypertrophic_cardiomyopathy|See_cases|not_provided|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|See_cases|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 3,
    "Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "not_provided|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Primary_dilated_cardiomyopathy|Neuromuscular_disease|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "See_cases|not_specified|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|not_specified|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_provided|Hypertrophic_cardiomyopathy_1|Left_ventricular_noncompaction_5|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Idiopathic_camptocormia|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder": 8,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy": 7,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_5|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|MYH7-related_disorder|not_specified|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiomyopathy|Myosin_storage_myopathy|not_provided|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S": 1,
    "not_specified|MYH7-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 3,
    "Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "not_specified|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Polymorphic_ventricular_tachycardia|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Atrial_fibrillation|Atrial_flutter|Tachycardia|Abnormal_morphology_of_left_ventricular_trabeculae": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Distal_muscle_weakness": 1,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 2,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Asymmetric_septal_hypertrophy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Pericarditis": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1S|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 3,
    "MYH7-related_disorder|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 4,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy": 1,
    "not_provided|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|MYH7-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "MYH7-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S|not_specified": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "not_provided|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Congenital_muscular_dystrophy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|MYH7-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Cardiomyopathy|MYH7-related_skeletal_myopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 5,
    "Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 2,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy": 1,
    "Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_disorder|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|Ventricular_fibrillation|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|See_cases": 1,
    "Myopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 3,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|not_specified": 2,
    "Cardiovascular_phenotype|not_provided|MYH7-related_skeletal_myopathy|Abnormality_of_the_musculature|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_beta-myosin_heavy_chain_(MYH7)|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1A": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy": 1,
    "Myosin_storage_myopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 2,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_1|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Myosin_storage_myopathy|not_provided|not_specified|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 4,
    "not_specified|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 4,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|MYH7-related_disorder": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Conduction_disorder_of_the_heart|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|First_degree_atrioventricular_block": 1,
    "Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Cardiomyopathy": 1,
    "MYH7-related_disorder|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Autosomal_dominant_MYH7-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 3,
    "MYH7-related_disorder|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy_1|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Myosin_storage_myopathy|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|Myosin_storage_myopathy|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Conduction_disorder_of_the_heart": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|not_specified": 1,
    "Cardiovascular_phenotype|Congenital_myopathy|not_provided|MYH7-related_skeletal_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Restrictive_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|MYH7-related_disorder|not_provided|Cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|MYH7-related_disorder|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|not_provided|Cardiomyopathy|not_specified|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy": 1,
    "Myosin_storage_myopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiomyopathy": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|MYH7-related_skeletal_myopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|MYH7-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Sudden_unexplained_death|not_specified|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Scapuloperoneal_myopathy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|not_provided|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|MYH7-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Myosin_storage_myopathy|Cardiomyopathy|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "MYH7-related_disorder|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|Cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|not_specified|not_provided|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Hypertrophic_cardiomyopathy|not_specified|Myosin_storage_myopathy|Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_1|Primary_dilated_cardiomyopathy|Myosin_storage_myopathy|Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1": 2,
    "MYH7-related_disorder|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|not_specified|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Myosin_storage_myopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|MYH7-related_disorder|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 3,
    "MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|MYH7-related_disorder|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_specified": 1,
    "Exertional_Heat_Illness|Hypertrophic_cardiomyopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_provided|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|MYH7-related_disorder|Ventricular_fibrillation|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|not_specified|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|not_specified": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1S|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 19,
    "Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|not_specified|not_provided|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Primary_dilated_cardiomyopathy|Sudden_cardiac_death|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_disorder|Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Myosin_storage_myopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_provided": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 2,
    "MYH7-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_2|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_9|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Left_ventricular_noncompaction_1|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Myosin_storage_myopathy|Cardiomyopathy|Craniosynostosis_4|Epicanthus|Muscular_ventricular_septal_defect|Delayed_gross_motor_development|Sagittal_craniosynostosis|Primary_dilated_cardiomyopathy|Delayed_speech_and_language_development|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Ebstein_anomaly|Cardiovascular_phenotype|Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|MYH7-related_disorder|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|Hypertrophic_cardiomyopathy|Dyspnea|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_provided|MYH7-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S|not_provided": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|MYH7-related_disorder|not_provided": 1,
    "Sudden_unexplained_death|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Inborn_genetic_diseases|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 3,
    "Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|not_specified|not_provided|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Ventricular_fibrillation|_paroxysmal_familial|_type_1|MYH7-related_skeletal_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "not_specified|Cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|MYH7-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|See_cases|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "MYH7-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Familial_cardiomyopathy": 23,
    "Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|not_provided|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Myosin_storage_myopathy|Scapuloperoneal_myopathy|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Myosin_storage_myopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiomyopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 10,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Scapuloperoneal_myopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|Increased_left_ventricular_wall_thickness|Left_ventricular_noncompaction|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "not_provided|Hypertrophic_cardiomyopathy|See_cases|not_specified|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|not_provided": 3,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Scapuloperoneal_myopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 2,
    "Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|MYH7-related_skeletal_myopathy|not_provided|Myosin_storage_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|not_specified": 2,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "MYH7-related_disorder|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided|Scapuloperoneal_myopathy|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Dilated_cardiomyopathy_1S": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_1|Familial_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|MYH7-related_disorder|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Biventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided": 1,
    "Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "Heart_failure|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_cardiomyopathy|MYH7-related_disorder|Hypertrophic_cardiomyopathy|Chest_pain|not_provided|Dilated_cardiomyopathy_1S|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|MYH7-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Ventricular_tachycardia": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Myopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_provided": 1,
    "not_provided|MYH7-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_provided": 3,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Familial_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1S|Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_hypertrophy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|not_specified": 58,
    "Cardiovascular_phenotype|Familial_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Wolff-Parkinson-White_pattern|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|MYH7-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Myosin_storage_myopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Restrictive_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_hypertrophic|_midventricular|_digenic|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiomyopathy|not_provided": 1,
    "not_provided|MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|not_specified": 1,
    "not_specified|Familial_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Familial_cardiomyopathy": 1,
    "Familial_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|MYH7-related_disorder|not_provided|Cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|MYH7-related_disorder|not_provided": 1,
    "MYH7-related_disorder|not_specified": 1,
    "Cardiomyopathy|MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_1": 59,
    "Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|MYH7-related_disorder": 1,
    "not_provided|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Cardiomyopathy|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Familial_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_specified|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|Myosin_storage_myopathy|not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Familial_cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 3,
    "not_provided|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_specified|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy": 1,
    "not_specified|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "MYH7-related_disorder|not_provided": 2,
    "Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_provided|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|MYH7-related_skeletal_myopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Familial_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Myosin_storage_myopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|MYH7-related_skeletal_myopathy": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|not_specified": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_specified|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiomyopathy|Hyaline_body_myopathy": 1,
    "Cardiovascular_phenotype|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_specified": 2,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Familial_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|MYH7-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy": 1,
    "Cardiomyopathy|Familial_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive": 1,
    "not_provided|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|not_specified": 1,
    "Myosin_storage_myopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy|Restrictive_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy": 2,
    "not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "MYH7-related_disorder|Myosin_storage_myopathy|Cardiovascular_phenotype|Dilated_Cardiomyopathy|_Dominant|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Biventricular_noncompaction_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Myosin_storage_myopathy|not_provided|Left_ventricular_noncompaction|Dilated_cardiomyopathy_1S": 1,
    "Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|not_provided|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_1S": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Myosin_storage_myopathy|not_provided|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1S": 1,
    "not_provided|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Left_ventricular_noncompaction|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|MYH7-related_skeletal_myopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|not_specified|not_provided|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiomyopathy|not_specified": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Primary_familial_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|not_specified|MYH7-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|not_specified|Myosin_storage_myopathy": 1,
    "Cardiovascular_phenotype|MYH7-related_disorder|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Left_ventricular_noncompaction_5|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S": 1,
    "not_provided|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S": 1,
    "Dilated_cardiomyopathy_1S|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 4,
    "Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Cardiovascular_phenotype|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|Cardiovascular_phenotype|Cardiomyopathy|MYH7-related_skeletal_myopathy|Primary_familial_hypertrophic_cardiomyopathy|Scapuloperoneal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction": 1,
    "Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|not_specified|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive": 1,
    "not_provided|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Left_ventricular_noncompaction_5|Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy_1": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_1S|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Wolff-Parkinson-White_pattern|Left_ventricular_noncompaction_5|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Cardiovascular_phenotype|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|not_specified|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|See_cases": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|not_specified": 4,
    "MYH7-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Myocarditis|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Cardiomyopathy": 1,
    "MYH7-related_disorder|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|MYH7-related_skeletal_myopathy|not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy": 1,
    "Cardiovascular_phenotype|Myosin_storage_myopathy|not_provided|Myopathy|_myosin_storage|_autosomal_recessive|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Cardiovascular_phenotype": 1,
    "Primary_familial_dilated_cardiomyopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1S|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Familial_cardiomyopathy|MYH7-related_disorder|Cardiomyopathy": 1,
    "not_provided|MYH7-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 2,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Congenital_myopathy|not_specified|not_provided|Cardiomyopathy|See_cases|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Scapuloperoneal_myopathy|MYH7-related_skeletal_myopathy|Dilated_Cardiomyopathy|_Dominant": 2,
    "not_provided|Hypertrophic_cardiomyopathy|MYH7-related_disorder": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Inborn_genetic_diseases|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiovascular_phenotype": 1,
    "not_specified|MYH7-related_disorder|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Myosin_storage_myopathy|not_specified|MYH7-related_skeletal_myopathy": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "not_provided|MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1S": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Restrictive_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "MYH7-related_disorder|not_provided|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1": 1,
    "MYH7-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|not_provided": 1,
    "MYH7-related_disorder|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Dilated_Cardiomyopathy|_Dominant|Cardiovascular_phenotype|not_provided|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Cardiomyopathy|not_specified|Myopathy|_myosin_storage|_autosomal_recessive": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Scapuloperoneal_myopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy": 1,
    "Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_disorder|Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|Congenital_myopathy_with_fiber_type_disproportion|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Myosin_storage_myopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Myopathy|_myosin_storage|_autosomal_recessive|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy|Dilated_cardiomyopathy_1S|Hypertrophic_cardiomyopathy": 1,
    "MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_provided|Myosin_storage_myopathy|Dilated_cardiomyopathy_1S|not_specified": 1,
    "Myopathy|_myosin_storage|_autosomal_recessive|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1S|Myosin_storage_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Myosin_storage_myopathy|MYH7-related_skeletal_myopathy|Myopathy|_myosin_storage|_autosomal_recessive|not_provided|Dilated_cardiomyopathy_1S": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Myosin_storage_myopathy|Hypertrophic_cardiomyopathy_1|MYH7-related_skeletal_myopathy": 1,
    "Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Scapuloperoneal_myopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_provided|Myosin_storage_myopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|MYH7-related_skeletal_myopathy|Hypertrophic_cardiomyopathy_1|Dilated_Cardiomyopathy|_Dominant": 1,
    "ZFHX2-related_disorder|not_provided": 3,
    "ZFHX2-related_disorder": 25,
    "ZFHX2-related_disorder|not_specified": 1,
    "not_specified|ZFHX2-related_disorder": 8,
    "Indifference_to_pain|_congenital|_autosomal_dominant|ZFHX2-related_disorder|not_provided": 1,
    "Indifference_to_pain|_congenital|_autosomal_dominant": 6,
    "not_provided|ZFHX2-related_disorder": 6,
    "not_provided|Indifference_to_pain|_congenital|_autosomal_dominant|ZFHX2-related_disorder": 1,
    "Indifference_to_pain|_congenital|_autosomal_dominant|not_provided|not_specified": 1,
    "Indifference_to_pain|_congenital|_autosomal_dominant|not_provided": 1,
    "not_provided|Indifference_to_pain|_congenital|_autosomal_dominant": 1,
    "Indifference_to_pain|_congenital|_autosomal_dominant|not_specified|not_provided": 1,
    "Indifference_to_pain|_congenital|_autosomal_dominant|not_specified": 1,
    "ENHANCED_S-CONE_SYNDROME_2|Retinitis_pigmentosa": 1,
    "not_provided|NRL-related_disorder": 3,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_27|NRL-related_disorder": 1,
    "Retinitis_pigmentosa_27": 5,
    "ENHANCED_S-CONE_SYNDROME_2|not_provided": 1,
    "Choroidal_neovascularization|Albinism|Elevated_circulating_hepatic_transaminase_concentration|Abnormality_of_metabolism/homeostasis|Foveal_hypoplasia|Slow_decrease_in_visual_acuity|not_provided": 1,
    "Retinal_dystrophy|ENHANCED_S-CONE_SYNDROME_2": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_27": 1,
    "not_provided|Retinitis_pigmentosa_27": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_27": 1,
    "ENHANCED_S-CONE_SYNDROME_2|not_provided|Retinitis_pigmentosa_27": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_27": 1,
    "Retinitis_pigmentosa_27|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_27|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_27": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_27": 1,
    "not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial|not_specified": 2,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial|not_specified|not_provided": 1,
    "not_provided|PCK2-related_disorder|not_specified": 1,
    "not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial": 3,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial": 2,
    "PCK2-related_disorder": 7,
    "PCK2-related_neuropathy|not_provided": 1,
    "Retinitis_pigmentosa_27|not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial": 1,
    "PCK2-related_disorder|not_provided": 3,
    "PCK2-related_disorder|not_specified": 1,
    "PCK2-related_disorder|not_provided|not_specified": 1,
    "not_provided|Phosphoenolpyruvate_carboxykinase_(GTP)_deficiency": 4,
    "not_provided|PCK2-related_disorder": 5,
    "Phosphoenolpyruvate_carboxykinase_(GTP)_deficiency": 9,
    "not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial|PCK2-related_disorder": 1,
    "PCK2-related_disorder|not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial": 2,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial|not_provided|PCK2-related_disorder": 1,
    "not_specified|not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_mitochondrial": 1,
    "Immunodeficiency_115_with_autoinflammation": 2,
    "RNF31-related_disorder|not_provided": 9,
    "RNF31-related_disorder|not_specified|not_provided": 1,
    "not_specified|Immunodeficiency_115_with_autoinflammation|not_provided": 1,
    "not_provided|Immunodeficiency_115_with_autoinflammation": 1,
    "not_provided|RNF31-related_disorder": 4,
    "not_specified|not_provided|RNF31-related_disorder": 1,
    "RNF31-related_disorder": 1,
    "not_provided|Polyglucosan_body_myopathy_type_1": 17,
    "not_provided|not_specified|Short_stature": 1,
    "IRF9-related_disorder|not_provided": 3,
    "Immunodeficiency_65|_susceptibility_to_viral_infections|not_provided": 1,
    "Immunodeficiency_65|_susceptibility_to_viral_infections|not_specified": 1,
    "Immunodeficiency_65|_susceptibility_to_viral_infections": 2,
    "not_provided|Immunodeficiency_65|_susceptibility_to_viral_infections": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_3|Revesz_syndrome": 12,
    "TINF2-related_disorder": 3,
    "Revesz_syndrome": 2,
    "TINF2-related_disorder|Dyskeratosis_congenita": 5,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3|Revesz_syndrome": 7,
    "not_specified|not_provided|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 5,
    "Dyskeratosis_congenita|_autosomal_dominant_3|not_provided|Dyskeratosis_congenita|Revesz_syndrome": 1,
    "Dyskeratosis_congenita|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "TINF2-related_disorder|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_dominant_3|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|TINF2-related_disorder": 3,
    "not_provided|TINF2-related_disorder|Dyskeratosis_congenita|not_specified": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3|Revesz_syndrome": 2,
    "Dyskeratosis_congenita|not_provided|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Revesz_syndrome|not_specified|Dyskeratosis_congenita|TINF2-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_3|not_provided": 1,
    "Dyskeratosis_congenita|Revesz_syndrome": 1,
    "Dyskeratosis_congenita|not_provided|not_specified": 1,
    "Dyskeratosis_congenita|See_cases|TINF2-related_disorder": 1,
    "Dyskeratosis_congenita|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|not_specified": 1,
    "Revesz_syndrome|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 2,
    "not_specified|Dyskeratosis_congenita|TINF2-related_disorder": 1,
    "Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita": 5,
    "Inherited_Immunodeficiency_Diseases|Dyskeratosis_congenita": 1,
    "not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3|Revesz_syndrome|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita": 5,
    "Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|_autosomal_dominant_1|Hoyeraal-Hreidarsson_syndrome|not_provided|Dyskeratosis_congenita": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_1|not_provided|TINF2-related_disorder": 1,
    "Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_1|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|not_provided|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Pulmonary_fibrosis|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|not_specified": 1,
    "not_provided|TINF2-related_disorder|Long_telomere_syndrome|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_3|TINF2-related_disorder|Revesz_syndrome|not_provided|not_specified|Dyskeratosis_congenita": 1,
    "Revesz_syndrome|Dyskeratosis_Congenita|_Dominant|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|_autosomal_dominant_1|not_specified|not_provided|Dyskeratosis_congenita|Malignant_tumor_of_breast": 1,
    "not_specified|Dyskeratosis_congenita|TINF2-related_disorder|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_3|Revesz_syndrome|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|Revesz_syndrome|TINF2-related_disorder": 1,
    "Revesz_syndrome|Dyskeratosis_Congenita|_Dominant": 2,
    "not_specified|Revesz_syndrome|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Long_telomere_syndrome": 2,
    "Dyskeratosis_congenita|TINF2-related_disorder|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_dominant_3|Revesz_syndrome|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|Dyskeratosis_Congenita|_Dominant|Revesz_syndrome": 1,
    "not_provided|not_specified|Dyskeratosis_congenita": 4,
    "Dyskeratosis_congenita|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|_autosomal_dominant_1|Revesz_syndrome|not_provided|Dyskeratosis_congenita": 1,
    "Long_telomere_syndrome|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|TINF2-related_disorder": 1,
    "Dyskeratosis_congenita|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|not_provided": 1,
    "Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3|Dyskeratosis_congenita|not_provided": 1,
    "not_provided|Revesz_syndrome|TINF2-related_disorder|not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Revesz_syndrome|not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3": 4,
    "Revesz_syndrome|not_provided|Dyskeratosis_congenita|_autosomal_dominant_3": 1,
    "not_provided|Revesz_syndrome|Dyskeratosis_congenita|_autosomal_dominant_3": 3,
    "Autosomal_recessive_congenital_ichthyosis_1|not_provided": 53,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_1": 96,
    "Autosomal_recessive_congenital_ichthyosis_1|not_provided|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_congenital_ichthyosis_1|TGM1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_congenital_ichthyosis_1": 2,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_1|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_congenital_ichthyosis_1|not_specified": 2,
    "not_provided|TGM1-related_disorder": 3,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_1|not_specified": 1,
    "Autosomal_recessive_congenital_ichthyosis_1|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_1|TGM1-related_disorder": 5,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_1": 2,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_1|not_provided": 4,
    "TGM1-related_disorder|not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_1": 5,
    "TGM1-related_disorder|not_provided": 4,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_1": 8,
    "Autosomal_recessive_congenital_ichthyosis_1|Ichthyosis": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_1": 6,
    "TGM1-related_disorder|not_provided|Autosomal_recessive_congenital_ichthyosis_1": 3,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_1|Lamellar_ichthyosis": 2,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_1|not_provided|Abnormality_of_the_skin": 2,
    "TGM1-related_disorder|Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_1|Abnormality_of_the_skin": 1,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_1|not_provided": 4,
    "Autosomal_recessive_congenital_ichthyosis_1|not_provided|TGM1-related_disorder": 2,
    "Autosomal_recessive_congenital_ichthyosis_1|not_provided|Lamellar_ichthyosis": 3,
    "TGM1-related_disorder|Autosomal_recessive_congenital_ichthyosis|not_provided|Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "TGM1-related_disorder|Autosomal_recessive_congenital_ichthyosis_1|not_provided": 1,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_1": 2,
    "Lamellar_ichthyosis|not_provided|Treacher_Collins_syndrome_1|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "not_provided|Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_1|Congenital_ichthyosiform_erythroderma": 1,
    "TGM1-related_disorder": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_1|Abnormality_of_the_skin": 1,
    "Autosomal_recessive_congenital_ichthyosis_1|not_provided|Abnormality_of_the_skin": 1,
    "Autosomal_recessive_congenital_ichthyosis_1|Lamellar_ichthyosis": 1,
    "Autosomal_recessive_congenital_ichthyosis_1|TGM1-related_disorder": 1,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_1|TGM1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "Autosomal_recessive_congenital_ichthyosis_1|TGM1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Wilms_tumor_predisposition": 2,
    "NYNRIN-related_disorder": 7,
    "not_provided|NYNRIN-related_disorder": 4,
    "not_provided|NYNRIN-related_disorder|not_specified": 1,
    "Predisposition_to_Wilms_tumor|not_specified|not_provided": 1,
    "Predisposition_to_Wilms_tumor|not_specified": 1,
    "not_provided|not_specified|NYNRIN-related_disorder": 1,
    "not_specified|Predisposition_to_Wilms_tumor": 1,
    "Wilms_tumor_predisposition|not_provided": 1,
    "not_provided|not_specified|Predisposition_to_Wilms_tumor": 2,
    "not_specified|not_provided|Predisposition_to_Wilms_tumor": 1,
    "not_specified|NYNRIN-related_disorder": 1,
    "NYNRIN-related_disorder|not_specified": 1,
    "not_provided|Rett_syndrome|_congenital_variant": 28,
    "Rett_syndrome|_congenital_variant": 451,
    "Rett_syndrome|_congenital_variant|not_specified": 11,
    "Rett_syndrome|_congenital_variant|not_provided": 24,
    "FOXG1_disorder|Inborn_genetic_diseases|Rett_syndrome|_congenital_variant": 3,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases|not_provided": 2,
    "FOXG1_disorder|Inborn_genetic_diseases|not_provided|Rett_syndrome|_congenital_variant": 3,
    "FOXG1_disorder": 2,
    "not_provided|FOXG1_disorder|Rett_syndrome|_congenital_variant": 1,
    "FOXG1-related_disorder|FOXG1_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant": 2,
    "not_provided|Rett_syndrome|_congenital_variant|FOXG1_disorder": 4,
    "not_specified|FOXG1-related_disorder|Rett_syndrome|_congenital_variant|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Rett_syndrome|_congenital_variant": 5,
    "FOXG1_disorder|not_specified|Inborn_genetic_diseases|Rett_syndrome|_congenital_variant": 1,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases": 8,
    "FOXG1-related_disorder|Rett_syndrome|_congenital_variant": 2,
    "not_specified|not_provided|Rett_syndrome|_congenital_variant": 2,
    "FOXG1_disorder|not_provided|Rett_syndrome|_congenital_variant": 12,
    "not_specified|Rett_syndrome|_congenital_variant": 7,
    "Inborn_genetic_diseases|not_provided|not_specified|Rett_syndrome|_congenital_variant": 1,
    "Inborn_genetic_diseases|Rett_syndrome|_congenital_variant": 11,
    "Rett_syndrome|_congenital_variant|not_provided|FOXG1_disorder": 2,
    "FOXG1_disorder|not_provided|Inborn_genetic_diseases|Rett_syndrome|_congenital_variant": 1,
    "FOXG1-related_disorder": 8,
    "FOXG1_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome|_congenital_variant": 2,
    "FOXG1-related_disorder|Inborn_genetic_diseases|FOXG1_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant": 2,
    "Inborn_genetic_diseases|Rett_syndrome|_congenital_variant|FOXG1_disorder|not_provided": 2,
    "Inborn_genetic_diseases|FOXG1-related_disorder|FOXG1_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant": 1,
    "Inborn_genetic_diseases|FOXG1-related_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant": 1,
    "FOXG1-related_disorder|FOXG1_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome|_congenital_variant": 2,
    "Inborn_genetic_diseases|FOXG1_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant": 2,
    "FOXG1-related_disorder|FOXG1_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome|_congenital_variant|Intellectual_disability": 1,
    "not_provided|Rett_syndrome|_congenital_variant|Inborn_genetic_diseases": 2,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases|not_provided|FOXG1_disorder|not_specified": 1,
    "Rett_syndrome|_congenital_variant|FOXG1-related_disorder|Inborn_genetic_diseases": 1,
    "Rett_syndrome|_congenital_variant|FOXG1_disorder": 10,
    "Rett_syndrome|_congenital_variant|FOXG1_disorder|not_specified": 1,
    "FOXG1-related_disorder|Inborn_genetic_diseases|Rett_syndrome|_congenital_variant": 1,
    "not_provided|Rett_syndrome|_congenital_variant|not_specified": 2,
    "not_provided|FOXG1-related_disorder": 1,
    "FOXG1_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant|Inborn_genetic_diseases": 1,
    "FOXG1_disorder|FOXG1-related_disorder|not_provided|Rett_syndrome|_congenital_variant|Abnormality_of_the_nervous_system": 1,
    "Rett_syndrome|_congenital_variant|Rett_syndrome|not_provided|FOXG1_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Rett_syndrome|_congenital_variant|FOXG1_disorder|not_specified": 1,
    "Inborn_genetic_diseases|FOXG1_disorder|not_provided|Rett_syndrome|_congenital_variant": 2,
    "FOXG1_disorder|Rett_syndrome|_congenital_variant": 13,
    "Inborn_genetic_diseases|not_specified|Rett_syndrome|_congenital_variant|FOXG1_disorder": 1,
    "not_provided|Rett_syndrome|_congenital_variant|FOXG1_disorder|Inborn_genetic_diseases": 1,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases|not_specified": 2,
    "Rett_syndrome|not_provided|Rett_syndrome|_congenital_variant": 1,
    "Inborn_genetic_diseases|Rett_syndrome|_congenital_variant|not_provided|FOXG1_disorder": 1,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases|FOXG1_disorder": 2,
    "Rett_syndrome|_congenital_variant|FOXG1-related_disorder": 1,
    "FOXG1_disorder|not_specified|not_provided|Rett_syndrome|_congenital_variant": 3,
    "FOXG1-related_disorder|FOXG1_disorder|Rett_syndrome|_congenital_variant|not_specified": 1,
    "Rett_syndrome|_congenital_variant|not_provided|FOXG1-related_disorder|FOXG1_disorder": 1,
    "not_provided|FOXG1_disorder|not_specified|Rett_syndrome|_congenital_variant": 1,
    "not_specified|Rett_syndrome|_congenital_variant|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|FOXG1_disorder|FOXG1-related_disorder|not_provided|Rett_syndrome|_congenital_variant|Abnormal_cerebral_morphology": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Rett_syndrome|_congenital_variant|FOXG1_disorder": 1,
    "Inborn_genetic_diseases|Rett_syndrome|_congenital_variant|FOXG1_disorder": 1,
    "Rett_syndrome|_congenital_variant|FOXG1-related_disorder|not_provided": 1,
    "FOXG1_disorder|not_provided|Rett_syndrome|_congenital_variant|Intellectual_disability": 2,
    "FOXG1-related_disorder|FOXG1_disorder|Rett_syndrome|_congenital_variant|Inborn_genetic_diseases": 1,
    "FOXG1_disorder|FOXG1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome|_congenital_variant": 1,
    "not_provided|FOXG1_disorder|Inborn_genetic_diseases": 1,
    "FOXG1_disorder|Severe_intellectual_deficiency": 1,
    "Rett_syndrome|_congenital_variant|Rett_syndrome": 3,
    "Rett_syndrome|_congenital_variant|FOXG1_disorder|not_provided": 2,
    "Rett_syndrome|_congenital_variant|Rett_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Rett_syndrome|_congenital_variant|not_provided|FOXG1_disorder": 1,
    "not_provided|FOXG1_disorder": 1,
    "FOXG1_disorder|Inborn_genetic_diseases|not_provided|not_specified|Rett_syndrome|_congenital_variant": 1,
    "Axial_hypotonia|Stereotypic_movement_disorder|Global_developmental_delay|Abnormal_optic_nerve_morphology|Strabismus|Rett_syndrome|_congenital_variant": 1,
    "FOXG1_disorder|not_provided|Rett_syndrome|Rett_syndrome|_congenital_variant": 1,
    "FOXG1_disorder|Rett_syndrome|_congenital_variant|not_provided": 2,
    "not_provided|Rett_syndrome": 51,
    "Rett_syndrome|not_provided": 68,
    "FOXG1_disorder|not_specified|Rett_syndrome|_congenital_variant": 2,
    "Neurodevelopmental_disorder|Rett_syndrome|_congenital_variant": 1,
    "FOXG1_disorder|not_provided": 2,
    "FOXG1-related_disorder|Inborn_genetic_diseases|not_provided|Rett_syndrome|_congenital_variant": 1,
    "not_provided|Inborn_genetic_diseases|Rett_syndrome|_congenital_variant|FOXG1-related_disorder": 1,
    "Aplasia/Hypoplasia_of_the_corpus_callosum|Intellectual_disability|_severe|Primary_microcephaly": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome|_congenital_variant": 1,
    "Rett_syndrome|_congenital_variant|not_specified|Inborn_genetic_diseases|FOXG1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Rett_syndrome|_congenital_variant|not_specified": 1,
    "Inborn_genetic_diseases|Rett_syndrome|_congenital_variant|not_provided": 1,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases|Neurodevelopmental_abnormality": 1,
    "Rett_syndrome|_congenital_variant|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Rett_syndrome|_congenital_variant": 1,
    "Rett_syndrome|_congenital_variant|not_specified|not_provided": 1,
    "FOXG1-related_disorder|Inborn_genetic_diseases": 1,
    "Rett_syndrome|_congenital_variant|Neurodevelopmental_disorder": 1,
    "FOXG1_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "PRKD1-related_disorder": 18,
    "PRKD1-related_disorder|not_provided": 9,
    "not_provided|Congenital_heart_defects_and_ectodermal_dysplasia": 6,
    "not_specified|Congenital_heart_defects_and_ectodermal_dysplasia": 1,
    "Congenital_heart_defects_and_ectodermal_dysplasia|Neurodevelopmental_delay": 1,
    "Congenital_heart_defects_and_ectodermal_dysplasia|not_provided": 1,
    "Congenital_heart_defects_and_ectodermal_dysplasia|not_specified": 2,
    "PRKD1-related_disorder|not_specified": 1,
    "not_provided|PRKD1-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis|SCFD1-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_9": 38,
    "not_provided|COCH-related_disorder": 2,
    "COCH-related_disorder": 7,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9|Hearing_impairment": 1,
    "COCH-related_disorder|not_provided": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_9|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_9|not_specified": 1,
    "Hearing_loss|_autosomal_recessive_110|not_specified|not_provided": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_9|COCH-related_disorder": 2,
    "Hearing_loss|_autosomal_recessive_110|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9|Prelingual_sensorineural_hearing_impairment": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_9|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_9|Hereditary_hearing_loss_and_deafness|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "Hearing_loss|_autosomal_recessive_110|Hearing_impairment": 1,
    "Hearing_loss|_autosomal_recessive_110|Autosomal_dominant_nonsyndromic_hearing_loss_9": 2,
    "COCH-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_9|not_provided": 1,
    "COCH-related_disorder|not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "not_provided|COCH-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9|not_specified|Nonsyndromic_genetic_hearing_loss": 1,
    "Hearing_loss|_autosomal_recessive_110": 3,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_9": 2,
    "not_specified|Hearing_loss|_autosomal_recessive_110|Autosomal_dominant_nonsyndromic_hearing_loss_9|not_provided": 1,
    "not_provided|not_specified|COCH-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "not_provided|not_specified|COCH-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_9|not_provided|not_specified": 2,
    "COCH-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_9|Hearing_loss|_autosomal_recessive_110": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9|Rare_genetic_deafness": 1,
    "Hearing_loss|_autosomal_recessive_110|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_9": 1,
    "Hereditary_spastic_paraplegia_52": 9,
    "Hereditary_spastic_paraplegia_52|Hereditary_spastic_paraplegia|not_specified|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_52": 2,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_52": 3,
    "Hereditary_spastic_paraplegia_52|Inborn_genetic_diseases|Intellectual_disability|APS41-related_disorder|Neurodevelopmental_disorder|not_provided|Spastic_paraplegia": 1,
    "Neurodevelopmental_disorder|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_52": 3,
    "Hereditary_spastic_paraplegia_52|not_provided": 2,
    "AP4S1-related_disorder": 6,
    "AP4S1-related_disorder|not_provided|Hereditary_spastic_paraplegia_52|Intellectual_disability|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_52|Spastic_paraplegia|Spastic_Paraplegia_52|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "HECTD1-related_disorder|not_provided": 1,
    "HECTD1-related_disorder": 1,
    "HECTD1-associated_neurodevelopmental_disorder": 1,
    "not_specified|HECTD1-related_disorder": 1,
    "not_specified|NUBPL-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_21|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_oxidative_phosphorylation_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_21": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_1|NUBPL-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_specified|not_provided": 1,
    "not_provided|NUBPL-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_21": 1,
    "not_provided|NUBPL-related_disorder": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_21": 16,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|See_cases|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_21": 2,
    "NUBPL-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "NUBPL-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_21|Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "NUBPL-related_disorder|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|NUBPL-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_specified|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_21|Inborn_genetic_diseases": 1,
    "ARHGAP5-related_disorder": 2,
    "AKAP6-related_Intellectual_Disability": 1,
    "Spastic_paraplegia_90B|_autosomal_recessive": 1,
    "Spastic_paraplegia_90A|_autosomal_dominant": 1,
    "Nemaline_myopathy_7": 101,
    "not_provided|Nemaline_myopathy_7": 8,
    "Nemaline_myopathy_7|not_provided": 4,
    "Nemaline_myopathy_7|not_specified": 2,
    "Muscle_weakness|Nemaline_myopathy_7": 1,
    "not_specified|Nemaline_myopathy_7|not_provided|Nemaline_Myopathy|_Recessive": 1,
    "CFL2-related_disorder|Nemaline_myopathy_7": 1,
    "not_specified|Nemaline_myopathy_7": 2,
    "Centronuclear_myopathy|Nemaline_myopathy_7": 1,
    "Nemaline_myopathy_7|CFL2-related_disorder": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_7": 1,
    "not_specified|Nemaline_myopathy_7|not_provided": 1,
    "BAZ1A-related_disorder": 7,
    "VATER/VACTERL_association_with_CNS_malformations": 1,
    "not_provided|Neutropenia|_severe_congenital|_8|_autosomal_dominant": 1,
    "Shwachman-Diamond_syndrome_1|not_provided|Neutropenia|_severe_congenital|_8|_autosomal_dominant|Ciliary_dyskinesia|_primary|_40": 1,
    "Shwachman-Diamond_syndrome_1|Neutropenia|_severe_congenital|_8|_autosomal_dominant": 1,
    "Shwachman-Diamond_syndrome_1|Neutropenia|_severe_congenital|_8|_autosomal_dominant|not_specified|not_provided|SRP54-related_disorder": 1,
    "Neutropenia|_severe_congenital|_8|_autosomal_dominant|Shwachman-Diamond_syndrome_1|Inborn_genetic_diseases": 1,
    "SRP54-related_disorder": 1,
    "SRP54-related_disorder|not_provided": 1,
    "not_provided|SRP54-related_disorder": 5,
    "Neutropenia|_severe_congenital|_8|_autosomal_dominant|Shwachman-Diamond_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Neutropenia|_severe_congenital|_8|_autosomal_dominant": 1,
    "FAM177A1-related_disorder": 2,
    "Neurodevelopmental_disorder_with_white_matter_abnormalities_and_gait_disturbance": 2,
    "Mild_obesity|Dolichocephaly|Macrocephaly|Intellectual_disability": 1,
    "Gonadal_dysgenesis|_dysmorphic_facies|_retinal_dystrophy|_and_myopathy": 4,
    "PPP2R3C-related_disorder": 2,
    "Spermatogenic_failure_36|Gonadal_dysgenesis|_dysmorphic_facies|_retinal_dystrophy|_and_myopathy": 1,
    "Spermatogenic_failure_36": 1,
    "Gonadal_dysgenesis|_dysmorphic_facies|_retinal_dystrophy|_and_myopathy|Spermatogenic_failure_36": 2,
    "Gonadal_dysgenesis|_dysmorphic_facies|_retinal_dystrophy|_and_myopathy|Spermatogenic_failure_36|not_provided|PPP2R3C-related_disorder": 1,
    "Combined_oxidative_phosphorylation_deficiency_54": 5,
    "PRORP-related_disorder|not_provided": 1,
    "PRORP-related_disorder": 3,
    "Combined_oxidative_phosphorylation_deficiency_54|Childhood_onset_sensorineural_hearing_impairment|Lactic_acidosis|Leukoencephalopathy|Microcephaly|Hypertonia|Feeding_difficulties|Global_developmental_delay|Persistent_lactic_acidosis|Diffuse_white_matter_abnormalities": 2,
    "not_specified|Combined_oxidative_phosphorylation_deficiency_54|Perrault_syndrome_1|Childhood_onset_sensorineural_hearing_impairment": 1,
    "not_specified|Combined_oxidative_phosphorylation_deficiency_54": 1,
    "Leukoencephalopathy|not_specified|Combined_oxidative_phosphorylation_deficiency_54": 1,
    "PRORP-related_disorder|Combined_oxidative_phosphorylation_deficiency_54|Childhood_onset_sensorineural_hearing_impairment": 1,
    "Combined_oxidative_phosphorylation_deficiency_54|Perrault_syndrome_1": 1,
    "PSMA6-related_disorder": 2,
    "Myocardial_infarction|_susceptibility_to|PSMA6-related_disorder": 1,
    "Ectodermal_dysplasia_and_immunodeficiency_2|not_provided": 6,
    "Ectodermal_dysplasia_and_immunodeficiency_2": 265,
    "not_provided|not_specified|Ectodermal_dysplasia_and_immunodeficiency_2": 4,
    "Ectodermal_dysplasia_and_immunodeficiency_2|NFKBIA-related_disorder": 2,
    "Ectodermal_dysplasia_and_immunodeficiency_2|Inborn_genetic_diseases": 11,
    "NFKBIA-related_disorder": 3,
    "NFKBIA-related_disorder|Ectodermal_dysplasia_and_immunodeficiency_2": 4,
    "Inborn_genetic_diseases|Ectodermal_dysplasia_and_immunodeficiency_2": 7,
    "not_provided|Ectodermal_dysplasia_and_immunodeficiency_2": 9,
    "NFKBIA-related_disorder|not_specified|Ectodermal_dysplasia_and_immunodeficiency_2|not_provided": 1,
    "Ectodermal_dysplasia_and_immunodeficiency_2|not_provided|not_specified": 2,
    "not_specified|Ectodermal_dysplasia_and_immunodeficiency_2|not_provided": 1,
    "Inherited_Immunodeficiency_Diseases|Ectodermal_dysplasia_and_immunodeficiency_2": 1,
    "not_specified|Ectodermal_dysplasia_and_immunodeficiency_2": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_neonatal_respiratory_insufficiency|_and_thermodysregulation": 20,
    "RALGAPA1-related_disorder": 9,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_neonatal_respiratory_insufficiency|_and_thermodysregulation": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_neonatal_respiratory_insufficiency|_and_thermodysregulation|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_neonatal_respiratory_insufficiency|_and_thermodysregulation|not_provided": 2,
    "RALGAPA1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|RALGAPA1-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_neonatal_respiratory_insufficiency|_and_thermodysregulation": 1,
    "Benign_hereditary_chorea|Brain-lung-thyroid_syndrome": 18,
    "Benign_hereditary_chorea|not_provided|Brain-lung-thyroid_syndrome": 6,
    "Brain-lung-thyroid_syndrome|Benign_hereditary_chorea|not_provided": 2,
    "Brain-lung-thyroid_syndrome|Benign_hereditary_chorea": 5,
    "Benign_hereditary_chorea": 17,
    "Brain-lung-thyroid_syndrome": 45,
    "Brain-lung-thyroid_syndrome|not_provided": 9,
    "Brain-lung-thyroid_syndrome|Thyroid_cancer|_nonmedullary|_1|not_provided|Benign_hereditary_chorea": 1,
    "Brain-lung-thyroid_syndrome|Benign_hereditary_chorea|not_provided|not_specified": 1,
    "not_specified|not_provided|Brain-lung-thyroid_syndrome": 1,
    "NKX2-1-related_disorder": 4,
    "NKX2-1-related_disorder|not_provided": 1,
    "not_provided|Brain-lung-thyroid_syndrome|NKX2-1-related_disorder": 1,
    "NKX2-1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Benign_hereditary_chorea": 1,
    "Benign_hereditary_chorea|Brain-lung-thyroid_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Brain-lung-thyroid_syndrome": 2,
    "NKX2-1-related_disorder|not_provided|Brain-lung-thyroid_syndrome": 1,
    "Benign_hereditary_chorea|NKX2-1-related_disorder|Brain-lung-thyroid_syndrome": 1,
    "not_provided|Brain-lung-thyroid_syndrome": 4,
    "Inborn_genetic_diseases|Benign_hereditary_chorea|Neurodevelopmental_disorder": 1,
    "Hereditary_ataxia|Chorea|Brain-lung-thyroid_syndrome": 1,
    "Inborn_genetic_diseases|Benign_hereditary_chorea": 1,
    "Benign_hereditary_chorea|not_provided": 1,
    "Benign_hereditary_chorea|Brain-lung-thyroid_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Brain-lung-thyroid_syndrome|NKX2-1-related_disorder": 1,
    "not_provided|Thyroid_cancer|_nonmedullary|_1|Benign_hereditary_chorea|Brain-lung-thyroid_syndrome": 1,
    "not_provided|See_cases|Brain-lung-thyroid_syndrome": 1,
    "Interstitial_lung_disease_2|Inborn_genetic_diseases": 1,
    "not_provided|Benign_hereditary_chorea|Brain-lung-thyroid_syndrome": 1,
    "not_provided|NKX2-1-related_disorder": 1,
    "Benign_hereditary_chorea|NKX2-1-related_disorder|not_provided|Brain-lung-thyroid_syndrome": 1,
    "Tooth_agenesis|_selective|_3": 67,
    "Selective_tooth_agenesis": 4,
    "not_provided|Tooth_agenesis|_selective|_3": 1,
    "PAX9-related_disorder": 8,
    "Hypodontia|Tooth_agenesis|_selective|_3": 6,
    "Hypodontia|PAX9-related_disorder|Tooth_agenesis|_selective|_3": 1,
    "PAX9-related_disorder|Hypodontia|Tooth_agenesis|_selective|_3|not_provided": 1,
    "Hypodontia|not_provided": 3,
    "Hypodontia|Inborn_genetic_diseases": 1,
    "Tooth_agenesis|_selective|_3|Hypodontia": 2,
    "Hypodontia|not_provided|Tooth_agenesis|_selective|_3": 1,
    "PAX9-related_disorder|Hypodontia": 1,
    "Hypodontia|not_provided|PAX9-related_disorder|Tooth_agenesis|_selective|_3": 1,
    "Tooth_agenesis|_selective|_3|Hypodontia|not_provided": 2,
    "Inborn_genetic_diseases|Hypodontia": 1,
    "not_specified|not_provided|Tooth_agenesis|_selective|_3|Hypodontia": 1,
    "Inborn_genetic_diseases|Tooth_agenesis|_selective|_3|not_provided": 1,
    "Tooth_agenesis|_selective|_3|not_provided": 5,
    "Mitochondrial_DNA_depletion_syndrome_18": 3,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_18": 2,
    "not_specified|SLC25A21-related_disorder|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_18|not_provided": 1,
    "SLC25A21-related_disorder|not_provided": 1,
    "MIPOL1-related_disorder": 3,
    "not_specified|MIPOL1-related_disorder": 1,
    "Craniolenticulosutural_dysplasia": 83,
    "SEC23A-related_disorder": 3,
    "not_provided|Craniolenticulosutural_dysplasia": 4,
    "SEC23A-related_disorder|Craniolenticulosutural_dysplasia": 2,
    "Craniolenticulosutural_dysplasia|not_provided": 4,
    "Craniolenticulosutural_dysplasia|not_specified": 7,
    "Craniolenticulosutural_dysplasia|SEC23A-related_disorder": 1,
    "Craniolenticulosutural_dysplasia|not_provided|SEC23A-related_disorder": 1,
    "not_specified|Craniolenticulosutural_dysplasia": 3,
    "not_provided|SEC23A-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_epilepsy|_and_brain_atrophy": 3,
    "not_provided|TRAPPC6B-related_disorder": 2,
    "TRAPPC6B-related_disorder": 4,
    "TRAPPC6B-related_disorder|Neurodevelopmental_disorder_with_microcephaly|_epilepsy|_and_brain_atrophy|not_provided|TRAPPC6B-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "LRFN5-related_disorder": 10,
    "LRFN5-related_disorder|not_provided": 2,
    "Joubert_syndrome_37": 11,
    "Joubert_syndrome|Joubert_syndrome_37": 5,
    "Joubert_syndrome|Joubert_syndrome_37|not_provided": 1,
    "Brown_syndrome|not_specified": 1,
    "Brown_syndrome|not_provided": 1,
    "not_specified|Joubert_syndrome_37": 1,
    "FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Premature_ovarian_failure_15|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided": 1,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 14,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 19,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 25,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|Fanconi_anemia": 2,
    "not_provided|FANCM-related_disorder": 2,
    "FANCM-related_disorder": 10,
    "Fanconi_anemia|FANCM-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_specified|Fanconi_anemia": 5,
    "Inborn_genetic_diseases|not_provided|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|FANCM-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Fanconi_anemia": 35,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided": 42,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 3,
    "not_provided|Fanconi_anemia|Inborn_genetic_diseases": 36,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 13,
    "Premature_ovarian_failure_15|not_provided|Fanconi_anemia|not_specified": 2,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|FANCM-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Fanconi_anemia|Spermatogenic_failure_28": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|not_specified|FANCM-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|FANCM-related_disorder|Premature_ovarian_failure_15|Spermatogenic_failure_28|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 1,
    "not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 13,
    "Fanconi_anemia|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 3,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCM-related_disorder": 4,
    "Fanconi_anemia|not_provided|FANCM-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|FANCM-related_disorder|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|FANCM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 1,
    "FANCM-related_disorder|Fanconi_anemia|Spermatogenic_failure_28|not_provided": 1,
    "Premature_ovarian_failure_15|Fanconi_anemia|not_specified|not_provided": 3,
    "not_provided|Spermatogenic_failure_28|not_specified|Fanconi_anemia|FANCM-related_disorder": 1,
    "Fanconi_anemia|Spermatogenic_failure_28|not_provided|Premature_ovarian_failure_15|not_specified": 1,
    "Fanconi_anemia|Premature_ovarian_failure_15|not_provided": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia": 18,
    "Premature_ovarian_failure_15|not_specified|not_provided|Fanconi_anemia": 2,
    "FANCM-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 6,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15": 11,
    "Fanconi_anemia|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15": 16,
    "Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15": 4,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia|Inborn_genetic_diseases": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Inborn_genetic_diseases|Fanconi_anemia|FANCM-related_disorder": 1,
    "FANCM-related_disorder|Fanconi_anemia|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCM-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia": 2,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|not_specified|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28": 6,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|FANCM-related_disorder": 1,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15": 2,
    "FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia": 3,
    "Premature_ovarian_failure_15": 2,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|not_provided": 11,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Hereditary_cancer": 1,
    "Spermatogenic_failure_28|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia|FANCM-related_disorder|Premature_ovarian_failure_15": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Premature_ovarian_failure_15|Spermatogenic_failure_28|not_provided": 1,
    "Inborn_genetic_diseases|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Inborn_genetic_diseases|Fanconi_anemia": 3,
    "Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|not_provided": 3,
    "FANCM-related_disorder|Fanconi_anemia": 3,
    "not_specified|not_provided|Premature_ovarian_failure_15|Spermatogenic_failure_28|Fanconi_anemia": 1,
    "Spermatogenic_failure_28|not_provided|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|Premature_ovarian_failure_15|Spermatogenic_failure_28": 2,
    "Fanconi_anemia|Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Fanconi_anemia|Premature_ovarian_failure_15|Spermatogenic_failure_28": 2,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|FANCM-related_disorder|not_provided": 1,
    "not_specified|Fanconi_anemia|not_provided|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 2,
    "Fanconi_anemia|not_specified|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified|Fanconi_anemia": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer|Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|FANCM-related_disorder": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|FANCM-related_disorder|not_specified|Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_specified|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|FANCM-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|FANCM-related_disorder": 3,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided": 1,
    "FANCM-related_disorder|not_provided|Fanconi_anemia": 3,
    "not_provided|Fanconi_anemia|Spermatogenic_failure_28|FANCM-related_disorder": 1,
    "not_provided|Fanconi_anemia|Hereditary_cancer": 1,
    "FANCM-related_disorder|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Hereditary_cancer": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|Premature_ovarian_failure_15|Spermatogenic_failure_28|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|_complementation_group_M": 2,
    "Hereditary_cancer-predisposing_syndrome|Spermatogenic_failure_28|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Premature_ovarian_failure_15": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Premature_ovarian_failure_15|not_provided|Fanconi_anemia|FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 1,
    "not_provided|Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|FANCM-related_disorder": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 4,
    "not_provided|Inborn_genetic_diseases|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided|not_specified|Fanconi_anemia": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 2,
    "Fanconi_anemia|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|FANCM-related_disorder": 1,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|FANCM-related_disorder|Inborn_genetic_diseases": 1,
    "Spermatogenic_failure_28|FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Premature_ovarian_failure_15|Fanconi_anemia": 1,
    "FANCM-related_disorder|not_provided|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Premature_ovarian_failure_15|Spermatogenic_failure_28|Fanconi_anemia|not_specified|not_provided": 2,
    "Premature_ovarian_failure_15|not_specified|Fanconi_anemia|not_provided": 1,
    "Hereditary_cancer|Inborn_genetic_diseases|Fanconi_anemia|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Inborn_genetic_diseases": 2,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|Fanconi_anemia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|not_provided|Inborn_genetic_diseases": 1,
    "FANCM-related_disorder|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 2,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|FANCM-related_disorder|not_provided|Hepatoblastoma": 1,
    "not_provided|Inborn_genetic_diseases|FANCM-related_disorder|Fanconi_anemia": 1,
    "not_provided|FANCM-related_disorder|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Premature_ovarian_failure_15|Spermatogenic_failure_28|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Fanconi_anemia": 1,
    "FANCM-related_disorder|not_provided|Fanconi_anemia|not_specified": 1,
    "not_provided|Premature_ovarian_failure_15|Fanconi_anemia|FANCM-related_disorder": 1,
    "Spermatogenic_failure_28|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|FANCM-related_disorder": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified|not_provided": 1,
    "Premature_ovarian_failure_15|FANCM-related_disorder|Aplastic_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_A|not_provided|not_specified|Fanconi_anemia": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "not_specified|Fanconi_anemia|not_provided": 4,
    "Fanconi_anemia|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 2,
    "FANCM-related_disorder|not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Premature_ovarian_failure_15|Fanconi_anemia": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|not_provided|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Premature_ovarian_failure_15|not_provided|Inborn_genetic_diseases|Fanconi_anemia|FANCM-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|not_provided|FANCM-related_disorder|Fanconi_anemia": 1,
    "not_provided|not_specified|Fanconi_anemia|Inborn_genetic_diseases|FANCM-related_disorder": 1,
    "Premature_ovarian_failure_15|Fanconi_anemia|not_provided|not_specified": 1,
    "not_provided|Spermatogenic_failure_28|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 1,
    "not_specified|Fanconi_anemia|not_provided|Premature_ovarian_failure_15": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_specified|not_provided|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer|Fanconi_anemia|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|not_specified|FANCM-related_disorder": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Fanconi_anemia|FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|FANCM-related_disorder|Fanconi_anemia": 2,
    "not_specified|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|not_provided": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia|Hereditary_cancer": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|not_provided|not_specified": 1,
    "FANCM_Fanconi-like_genomic_instability_disorder": 1,
    "Fanconi_anemia|not_provided|not_specified|Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder": 1,
    "Hereditary_cancer|Fanconi_anemia": 2,
    "Premature_ovarian_failure_15|Spermatogenic_failure_28|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 27,
    "Fanconi_anemia|Premature_ovarian_failure_15": 1,
    "Premature_ovarian_failure_15|Spermatogenic_failure_28|Fanconi_anemia|not_provided|not_specified": 1,
    "Fanconi_anemia|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_specified": 1,
    "FANCM-related_disorder|Fanconi_anemia|not_provided|not_specified": 1,
    "not_specified|Fanconi_anemia|Hepatoblastoma": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_cancer-predisposing_syndrome|Premature_ovarian_failure_15|Spermatogenic_failure_28": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|not_specified|Fanconi_anemia|FANCM-related_disorder": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCM-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|FANCM-related_disorder": 1,
    "not_specified|Premature_ovarian_failure_15|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia": 1,
    "Fanconi_anemia|Spermatogenic_failure_28": 1,
    "Fanconi_anemia|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|Hereditary_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Spermatogenic_failure_28|Fanconi_anemia": 1,
    "Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided|Fanconi_anemia|FANCM-related_disorder|Familial_cancer_of_breast|Male_infertility_with_spermatogenesis_disorder|Fanconi_anemia_complementation_group_A": 1,
    "not_specified|not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|not_specified|Premature_ovarian_failure_15": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|not_provided|Premature_ovarian_failure_15|Spermatogenic_failure_28": 1,
    "not_specified|not_provided|Premature_ovarian_failure_15|Fanconi_anemia": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|FANCM-related_disorder|Fanconi_anemia": 2,
    "Spermatogenic_failure_28|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Fanconi_anemia|Inborn_genetic_diseases|FANCM-related_disorder": 1,
    "Fanconi_anemia|FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided": 30,
    "Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder|not_provided": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|not_provided|FANCM-related_disorder|Fanconi_anemia|_complementation_group_M": 1,
    "Fanconi_anemia|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 1,
    "not_specified|FANCM-related_disorder|Fanconi_anemia|Premature_ovarian_failure_15|not_provided": 1,
    "Fanconi_anemia|FANCM-related_disorder|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15": 1,
    "Fanconi_anemia|not_provided|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Spermatogenic_failure_28|Premature_ovarian_failure_15|Malignant_germ_cell_tumor_of_ovary|Azoospermia|not_specified|Hereditary_nonpolyposis_colorectal_carcinoma|Fanconi_anemia|not_provided|Familial_cancer_of_breast": 1,
    "FANCM-related_disorder|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases|not_provided|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer": 1,
    "Fanconi_anemia|Hereditary_cancer|Spermatogenic_failure_28|Premature_ovarian_failure_15|not_provided": 1,
    "not_provided|Fanconi_anemia|Spermatogenic_failure_28|Premature_ovarian_failure_15|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|Spermatogenic_failure_28|Premature_ovarian_failure_15|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|not_provided|Spermatogenic_failure_28|Premature_ovarian_failure_15|FANCM-related_disorder": 1,
    "FANCM-related_disorder|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Spermatogenic_failure_63|Spermatogenesis_maturation_arrest": 1,
    "MDGA2-related_intellectual_disability": 1,
    "RPS29-related_disorder": 3,
    "Diamond-Blackfan_anemia_13": 3,
    "Diamond-Blackfan_anemia_13|not_provided": 1,
    "not_provided|RPS29-related_disorder": 1,
    "not_provided|Diamond-Blackfan_anemia_13": 2,
    "MGAT2-congenital_disorder_of_glycosylation": 77,
    "MGAT2-congenital_disorder_of_glycosylation|not_provided|Congenital_disorder_of_glycosylation": 2,
    "MGAT2-congenital_disorder_of_glycosylation|Primary_ciliary_dyskinesia|not_provided|Congenital_disorder_of_glycosylation": 2,
    "MGAT2-congenital_disorder_of_glycosylation|MGAT2-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|MGAT2-congenital_disorder_of_glycosylation": 7,
    "MGAT2-related_disorder": 1,
    "Inborn_genetic_diseases|MGAT2-congenital_disorder_of_glycosylation|not_provided|not_specified|MGAT2-related_disorder": 1,
    "not_specified|MGAT2-congenital_disorder_of_glycosylation": 1,
    "MGAT2-related_disorder|MGAT2-congenital_disorder_of_glycosylation": 2,
    "Inborn_genetic_diseases|MGAT2-congenital_disorder_of_glycosylation|MGAT2-related_disorder": 1,
    "MGAT2-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "MGAT2-congenital_disorder_of_glycosylation|Primary_ciliary_dyskinesia|not_specified|not_provided|Congenital_disorder_of_glycosylation": 1,
    "MGAT2-congenital_disorder_of_glycosylation|not_specified": 4,
    "MGAT2-congenital_disorder_of_glycosylation|MGAT2-related_disorder": 1,
    "Global_developmental_delay|Abnormal_facial_shape|Abnormal_glycosylation|MGAT2-congenital_disorder_of_glycosylation": 1,
    "not_provided|MGAT2-congenital_disorder_of_glycosylation": 2,
    "MGAT2-congenital_disorder_of_glycosylation|not_provided": 1,
    "MGAT2-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_specified": 1,
    "MGAT2-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia|Congenital_disorder_of_glycosylation|not_provided|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia_10": 21,
    "Primary_ciliary_dyskinesia|not_provided|Congenital_disorder_of_glycosylation|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia|DNAAF2-related_disorder": 6,
    "Primary_ciliary_dyskinesia_10|Primary_ciliary_dyskinesia": 20,
    "DNAAF2-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10": 16,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Congenital_disorder_of_glycosylation|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia_10|Primary_ciliary_dyskinesia|not_specified": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10": 9,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10": 3,
    "DNAAF2-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10": 1,
    "DNAAF2-related_disorder": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10|DNAAF2-related_disorder|not_specified": 2,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_10": 1,
    "not_provided|Primary_ciliary_dyskinesia|DNAAF2-related_disorder|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia_10|Primary_ciliary_dyskinesia|not_specified|not_provided": 1,
    "not_provided|DNAAF2-related_disorder": 1,
    "Primary_ciliary_dyskinesia_10|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia_10|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia_10|DNAAF2-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_10|not_provided": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_10|not_specified": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_10|Primary_ciliary_dyskinesia": 1,
    "Kartagener_syndrome|Primary_ciliary_dyskinesia_10": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_10|not_specified": 1,
    "Primary_ciliary_dyskinesia_10|not_provided": 1,
    "POLE2-related_disorder": 1,
    "POLE2-related_disorder|not_provided": 6,
    "not_provided|POLE2-related_disorder|not_specified": 1,
    "not_provided|POLE2-related_disorder": 4,
    "not_provided|NEMF-related_disorder": 4,
    "Intellectual_developmental_disorder_with_speech_delay_and_axonal_peripheral_neuropathy": 12,
    "See_cases|Intellectual_developmental_disorder_with_speech_delay_and_axonal_peripheral_neuropathy": 1,
    "NEMF-related_disorder": 9,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_speech_delay_and_axonal_peripheral_neuropathy": 1,
    "not_provided|Intellectual_developmental_disorder_with_speech_delay_and_axonal_peripheral_neuropathy": 2,
    "NEMF-related_disorder|not_provided": 4,
    "Intellectual_developmental_disorder_with_speech_delay_and_axonal_peripheral_neuropathy|See_cases": 1,
    "Noonan_syndrome_9": 848,
    "Noonan_syndrome|Noonan_syndrome_9|not_specified": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_9": 140,
    "Noonan_syndrome_9|Cardiovascular_phenotype": 105,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_9": 3,
    "not_provided|Noonan_syndrome_9": 19,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_specified": 12,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_specified|not_provided|SOS2-related_disorder": 1,
    "Noonan_syndrome_9|SOS2-related_disorder": 5,
    "Cardiovascular_phenotype|not_provided|not_specified|SOS2-related_disorder|Noonan_syndrome_9": 1,
    "not_specified|Cardiovascular_phenotype|Noonan_syndrome_9": 8,
    "not_specified|Noonan_syndrome_9": 24,
    "Cardiovascular_phenotype|not_specified|Noonan_syndrome_9": 6,
    "not_provided|not_specified|Cardiovascular_phenotype|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|not_provided": 17,
    "SOS2-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_9|not_specified": 4,
    "Cardiovascular_phenotype|not_specified|Noonan_syndrome_9|not_provided": 1,
    "SOS2-related_disorder|Noonan_syndrome_9": 12,
    "SOS2-related_disorder|not_provided|Noonan_syndrome_9|not_specified": 1,
    "Noonan_syndrome_9|Cardiovascular_phenotype|not_specified": 3,
    "not_specified|RASopathy|Cardiovascular_phenotype|Noonan_syndrome_9|SOS2-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|SOS2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_9": 2,
    "Noonan_syndrome_9|not_provided|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_9|not_provided|Cardiovascular_phenotype|SOS2-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|SOS2-related_disorder|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|RASopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_specified|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_9|not_specified": 21,
    "Noonan_syndrome|Noonan_syndrome_9|not_provided": 1,
    "Cardiovascular_phenotype|SOS2-related_disorder|Noonan_syndrome_9": 6,
    "Noonan_syndrome_9|not_specified|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_specified|Noonan_syndrome_9|SOS2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|SOS2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_9|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Noonan_syndrome_9|not_specified": 2,
    "SOS2-related_disorder": 16,
    "not_specified|Noonan_syndrome_9|not_provided": 1,
    "SOS2-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_9": 3,
    "SOS2-related_disorder|not_specified|Noonan_syndrome_9|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_9|not_specified|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "not_specified|Noonan_syndrome_9|Cardiovascular_phenotype": 3,
    "not_specified|Cardiovascular_phenotype|not_provided|Noonan_syndrome|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|not_provided|SOS2-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_9|not_specified|not_provided": 1,
    "Noonan_syndrome_9|Cardiovascular_phenotype|not_provided": 2,
    "not_provided|RASopathy|Cardiovascular_phenotype|Noonan_syndrome_9": 1,
    "Cardiovascular_phenotype|SOS2-related_disorder|not_specified|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_9": 1,
    "Cardiovascular_phenotype|not_specified|SOS2-related_disorder|Noonan_syndrome_9": 2,
    "not_specified|not_provided|Noonan_syndrome_9": 3,
    "SOS2-related_disorder|Noonan_syndrome_9|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome_9|Cardiovascular_phenotype|See_cases": 1,
    "not_specified|SOS2-related_disorder|Noonan_syndrome_9": 1,
    "not_specified|Noonan_syndrome_9|not_provided|Cardiovascular_phenotype": 2,
    "Noonan_syndrome_9|not_specified|Cardiovascular_phenotype": 5,
    "Noonan_syndrome_9|SOS2-related_disorder|not_specified": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "SOS2-related_disorder|Noonan_syndrome_9|Cardiovascular_phenotype": 3,
    "not_provided|Noonan_syndrome_9|SOS2-related_disorder|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_9|Cardiovascular_phenotype|Noonan_syndrome_1": 1,
    "Noonan_syndrome_9|not_specified|not_provided|Noonan_syndrome|SOS2-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Noonan_syndrome_9|Noonan_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Noonan_syndrome_9|not_specified": 2,
    "not_provided|SOS2-related_disorder|Noonan_syndrome_9|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_9|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_9": 1,
    "SOS2-related_disorder|Noonan_syndrome_9|not_specified|not_provided": 1,
    "Noonan_syndrome_9|not_specified|not_provided": 2,
    "Noonan_syndrome_9|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Noonan_syndrome_9|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_provided": 3,
    "Noonan_syndrome_9|SOS2-related_disorder|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Noonan_syndrome_9|Noonan_syndrome": 2,
    "Noonan_syndrome_9|Congenital_heart_disease|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|SOS2-related_disorder": 1,
    "SOS2-related_disorder|not_provided|Noonan_syndrome_9": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_9": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_specified|not_provided": 1,
    "Noonan_syndrome|Cardiovascular_phenotype|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_9|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|not_provided|Noonan_syndrome|Noonan_syndrome_1": 1,
    "Noonan_syndrome|Noonan_syndrome_9": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Noonan_syndrome_9": 2,
    "Noonan_syndrome_9|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "not_provided|SOS2-related_disorder|Noonan_syndrome_9|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_9": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Noonan_syndrome_9|Cardiovascular_phenotype|not_specified": 1,
    "RASopathy|Noonan_syndrome|not_provided|Noonan_syndrome_9|SOS2-related_disorder": 1,
    "Noonan_syndrome_9|not_provided|RASopathy": 1,
    "Noonan_syndrome_9|Noonan_syndrome": 2,
    "Noonan_syndrome|not_provided|RASopathy|Noonan_syndrome_9": 1,
    "Noonan_syndrome_9|not_specified|SOS2-related_disorder|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_9|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|Noonan_syndrome_9|not_specified|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_9|not_provided": 1,
    "not_provided|not_specified|SOS2-related_disorder|Noonan_syndrome_9|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_9|not_specified|not_provided": 3,
    "Noonan_syndrome_9|Noonan_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Noonan_syndrome_9|not_specified|not_provided|Noonan_syndrome|SOS2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Noonan_syndrome_9|Cardiovascular_phenotype|SOS2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "Noonan_syndrome_9|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Noonan_syndrome_9": 1,
    "SOS2-related_disorder|not_provided": 1,
    "SOS2-related_disorder|Noonan_syndrome_9|not_provided": 1,
    "not_provided|SOS2-related_disorder|Noonan_syndrome_9|Cardiovascular_phenotype|not_specified": 1,
    "Male_infertility_due_to_gonadal_dysgenesis_or_sperm_disorder": 1,
    "L-2-hydroxyglutaric_aciduria": 172,
    "L-2-hydroxyglutaric_aciduria|Inborn_genetic_diseases": 8,
    "not_specified|L-2-hydroxyglutaric_aciduria": 3,
    "not_provided|not_specified|L-2-hydroxyglutaric_aciduria": 2,
    "Inborn_genetic_diseases|L-2-hydroxyglutaric_aciduria|not_specified|not_provided": 1,
    "L2HGDH-related_disorder|not_specified|L-2-hydroxyglutaric_aciduria": 1,
    "L2HGDH-related_disorder|not_specified|not_provided|L-2-hydroxyglutaric_aciduria": 1,
    "not_provided|L-2-hydroxyglutaric_aciduria|Inborn_genetic_diseases": 2,
    "L2HGDH-related_disorder|L-2-hydroxyglutaric_aciduria": 3,
    "Inborn_genetic_diseases|L-2-hydroxyglutaric_aciduria": 12,
    "L-2-hydroxyglutaric_aciduria|not_specified": 4,
    "not_provided|L-2-hydroxyglutaric_aciduria": 10,
    "not_specified|not_provided|L-2-hydroxyglutaric_aciduria|L2HGDH-related_disorder": 1,
    "L-2-hydroxyglutaric_aciduria|not_provided": 7,
    "L-2-hydroxyglutaric_aciduria|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|L-2-hydroxyglutaric_aciduria|not_provided": 2,
    "L2HGDH-related_disorder|not_provided|L-2-hydroxyglutaric_aciduria": 1,
    "L-2-hydroxyglutaric_aciduria|Abnormality_of_metabolism/homeostasis": 1,
    "L-2-hydroxyglutaric_aciduria|L2HGDH-related_disorder|not_specified|not_provided": 1,
    "not_specified|L-2-hydroxyglutaric_aciduria|L2HGDH-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|L-2-hydroxyglutaric_aciduria": 1,
    "L-2-hydroxyglutaric_aciduria|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|L-2-hydroxyglutaric_aciduria": 1,
    "Hereditary_spastic_paraplegia_3A": 347,
    "Hereditary_spastic_paraplegia_3A|not_provided|Inborn_genetic_diseases": 2,
    "Neuropathy|_hereditary_sensory|_type_1D|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A": 16,
    "Hereditary_spastic_paraplegia_3A|not_specified": 3,
    "not_specified|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A|not_provided": 2,
    "Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases": 7,
    "Hereditary_spastic_paraplegia_3A|not_provided": 25,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_3A|not_provided|Neuropathy|_hereditary_sensory|_type_1D": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_3A": 6,
    "Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases|not_provided": 1,
    "Neuropathy|_hereditary_sensory|_type_1D": 4,
    "not_specified|Hereditary_spastic_paraplegia_3A": 3,
    "not_provided|Neuropathy|_hereditary_sensory|_type_1D|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A": 1,
    "ATL1-related_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A": 2,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|not_specified": 1,
    "ATL1-related_disorder|Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia": 1,
    "Abnormal_pyramidal_sign|Hereditary_spastic_paraplegia_3A": 1,
    "not_provided|Hereditary_spastic_paraplegia_3A": 22,
    "Hereditary_spastic_paraplegia_3A|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_1D": 1,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory|_type_1D": 1,
    "ATL1-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|ATL1-related_disorder|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A|not_specified": 1,
    "Neuropathy|_hereditary_sensory|_type_1D|not_provided": 2,
    "Hereditary_spastic_paraplegia_3A|not_provided|ATL1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_3A|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided|ATL1-related_disorder|not_specified|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A|not_provided": 2,
    "Neuropathy|_hereditary_sensory|_type_1D|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_3A": 1,
    "Hereditary_spastic_paraplegia_3A|ATL1-related_disorder|Neuropathy|_hereditary_sensory|_type_1D|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_3A": 1,
    "Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D": 5,
    "Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases|not_specified": 3,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_3A": 1,
    "not_specified|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A": 1,
    "Neuropathy|_hereditary_sensory|_type_1D|not_provided|Hereditary_spastic_paraplegia_3A": 2,
    "Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A": 1,
    "Spastic_paraplegia|_autosomal_dominant|Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory|_type_1D|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_3A": 1,
    "Neuropathy|_hereditary_sensory|_type_1D|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia": 1,
    "Lingual_thyroid": 1,
    "Charcot-Marie-Tooth_disease|Neuropathy|_hereditary_sensory|_type_1D|Osteomyelitis_leading_to_amputation_due_to_slow_healing_fractures|Penetrating_foot_ulcers|Distal_sensory_impairment|Distal_lower_limb_muscle_weakness": 1,
    "ATL1-related_disorder|Hereditary_spastic_paraplegia_3A": 2,
    "not_specified|Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spastic_paraplegia_3A|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_3A|Accessory_ectopic_thyroid_tissue": 1,
    "Hereditary_spastic_paraplegia_3A|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|not_specified|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_3A": 1,
    "Hereditary_spastic_paraplegia_3A|Neuropathy|_hereditary_sensory|_type_1D|not_provided": 2,
    "Hereditary_spastic_paraplegia_3A|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|ATL1-related_spastic_paraplegia|_recessive": 1,
    "not_provided|Neuropathy|_hereditary_sensory|_type_1D|Hereditary_spastic_paraplegia_3A": 1,
    "Seckel_syndrome_7|not_provided": 2,
    "not_provided|Seckel_syndrome_7": 4,
    "NIN-related_disorder|not_specified|not_provided": 4,
    "Joubert_syndrome_3|Seckel_syndrome_7": 1,
    "Seckel_syndrome_7": 6,
    "not_specified|NIN-related_disorder|not_provided": 3,
    "NIN-related_disorder|Seckel_syndrome|not_provided": 1,
    "not_specified|not_provided|Seckel_syndrome_7": 8,
    "NIN-related_disorder|not_provided": 4,
    "not_provided|NIN-related_disorder": 7,
    "NIN-related_disorder": 6,
    "not_provided|Seckel_syndrome_7|not_specified": 4,
    "not_provided|not_specified|NIN-related_disorder": 1,
    "not_specified|NIN-related_disorder|not_provided|Seckel_syndrome_7": 2,
    "not_provided|not_specified|Seckel_syndrome_7": 2,
    "not_provided|NIN-related_disorder|not_specified": 2,
    "NIN-related_disorder|Seckel_syndrome_7|not_specified|not_provided": 1,
    "Glycogen_storage_disease|_type_VI": 199,
    "not_provided|not_specified|Glycogen_storage_disease|_type_VI": 6,
    "not_specified|not_provided|Glycogen_storage_disease|_type_VI": 5,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_VI|not_provided": 3,
    "Glycogen_storage_disease|_type_VI|not_specified": 2,
    "not_provided|PYGL-related_disorder": 1,
    "Glycogen_storage_disease|_type_VI|Inborn_genetic_diseases": 7,
    "PYGL-related_disorder": 7,
    "Glycogen_storage_disease|_type_VI|not_provided": 10,
    "not_provided|Glycogen_storage_disease|_type_VI|not_specified": 5,
    "not_specified|Glycogen_storage_disease|_type_VI": 2,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_VI": 7,
    "PYGL-related_disorder|not_provided|Glycogen_storage_disease|_type_VI": 2,
    "PYGL-related_disorder|Glycogen_storage_disease|_type_VI": 5,
    "Glycogen_storage_disease|_type_VI|PYGL-related_disorder": 3,
    "not_provided|Glycogen_storage_disease|_type_VI": 11,
    "Glycogen_storage_disease|_type_VI|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Glycogen_storage_disease|_type_VI": 1,
    "not_provided|Glycogen_storage_disease|_type_VI|not_specified|PYGL-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease|_type_VI": 2,
    "not_specified|Glycogen_storage_disease|_type_VI|PYGL-related_disorder|not_provided": 1,
    "Glycogen_storage_disease|_type_VI|PYGL-related_disorder|not_provided": 1,
    "Asthma-related_traits|_susceptibility_to|_1": 1,
    "Asthma|_aspirin-induced|_susceptibility_to": 1,
    "Rhizomelic_dysplasia|_Ain-Naz_type": 2,
    "not_provided|Hereditary_spastic_paraplegia_28": 9,
    "Hereditary_spastic_paraplegia_28": 281,
    "Hereditary_spastic_paraplegia_28|Hereditary_spastic_paraplegia": 4,
    "Hereditary_spastic_paraplegia_28|not_provided": 14,
    "Spasticity": 2,
    "Hereditary_spastic_paraplegia_28|Inborn_genetic_diseases": 6,
    "not_provided|DDHD1-related_disorder": 1,
    "not_provided|DDHD1-related_disorder|Hereditary_spastic_paraplegia_28": 1,
    "not_provided|Hereditary_spastic_paraplegia_28|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_28|not_provided": 1,
    "Hereditary_spastic_paraplegia_28|Inborn_genetic_diseases|not_provided|DDHD1-related_disorder|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_28|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_28": 19,
    "not_specified|Hereditary_spastic_paraplegia_28": 2,
    "Hereditary_spastic_paraplegia_28|not_specified|DDHD1-related_disorder|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_28|not_provided|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia_28|not_specified": 3,
    "Hereditary_spastic_paraplegia_28|not_provided|Hereditary_spastic_paraplegia": 2,
    "Inborn_genetic_diseases|DDHD1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_28": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_28": 2,
    "DDHD1-related_disorder|Hereditary_spastic_paraplegia_28": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_28": 2,
    "Hereditary_spastic_paraplegia_28|not_specified": 4,
    "Hereditary_spastic_paraplegia_28|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_28": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_28": 3,
    "Hereditary_spastic_paraplegia_28|not_specified|not_provided": 3,
    "Hereditary_spastic_paraplegia_28|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_28|Hereditary_spastic_paraplegia|not_specified": 1,
    "DDHD1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_28|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_28": 1,
    "Hereditary_spastic_paraplegia_28|Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_28": 1,
    "Hereditary_spastic_paraplegia_28|Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_28|DDHD1-related_disorder": 1,
    "Orofacial_cleft_11|Syndromic_Microphthalmia|_Dominant|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 3,
    "Orofacial_cleft_11": 5,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft|Orofacial_cleft_11": 1,
    "not_provided|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|BMP4-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Orofacial_cleft": 1,
    "not_provided|Orofacial_cleft|BMP4-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "Orofacial_cleft|BMP4-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant": 1,
    "not_provided|Syndromic_Microphthalmia|_Dominant|BMP4-Related_Syndromic_Microphthalmia|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Orofacial_cleft": 3,
    "Syndromic_Microphthalmia|_Dominant|BMP4-Related_Syndromic_Microphthalmia|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|not_provided|Orofacial_cleft": 1,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Syndromic_Microphthalmia|_Dominant|BMP4-Related_Syndromic_Microphthalmia|Orofacial_cleft": 1,
    "not_provided|Orofacial_cleft|Syndromic_Microphthalmia|_Dominant|Orofacial_cleft_11": 1,
    "Microphthalmia_with_brain_and_digit_anomalies|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|not_provided|Orofacial_cleft_11": 1,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Orofacial_cleft_11|Syndromic_Microphthalmia|_Dominant": 2,
    "Syndromic_Microphthalmia|_Dominant|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Orofacial_cleft_11": 1,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|not_provided|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 1,
    "Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 76,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 35,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|Inborn_genetic_diseases": 7,
    "BMP4-related_disorder": 12,
    "BMP4-related_disorder|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|Inborn_genetic_diseases": 1,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|BMP4-related_disorder": 2,
    "BMP4-related_disorder|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 2,
    "not_provided|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|BMP4-related_disorder": 1,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 1,
    "Inborn_genetic_diseases|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 9,
    "not_provided|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 1,
    "Microphthalmia_with_brain_and_digit_anomalies": 9,
    "BMP4-Related_Syndromic_Microphthalmia": 1,
    "Inborn_genetic_diseases|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 3,
    "BMP4-related_disorder|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 3,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|See_cases|BMP4-related_disorder|not_provided": 1,
    "Low_bone_mineral_density|Tooth_agenesis": 1,
    "Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|Inborn_genetic_diseases": 2,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|not_specified": 2,
    "not_specified|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 1,
    "Orofacial_cleft_11|not_provided|Microphthalmia_with_brain_and_digit_anomalies|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|not_specified": 1,
    "Kapur-Toriello_syndrome": 1,
    "Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|not_provided": 4,
    "Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|not_specified|not_provided": 1,
    "Syndromic_Microphthalmia|_Dominant|Orofacial_cleft|Orofacial_cleft_11": 1,
    "BMP4-related_disorder|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|not_provided": 1,
    "not_provided|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 1,
    "Orofacial_cleft_11|not_specified|not_provided|Microphthalmia_with_brain_and_digit_anomalies": 1,
    "BMP4-related_disorder|Inborn_genetic_diseases|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11": 1,
    "Microphthalmia_with_brain_and_digit_anomalies|not_provided": 1,
    "Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|Intellectual_disability|not_provided": 1,
    "Syndromic_Microphthalmia|_Dominant|Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|not_provided|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 1,
    "not_provided|Orofacial_cleft|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies|Congenital_heart_disease": 1,
    "not_provided|Inborn_genetic_diseases|Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|BMP4-related_disorder|Intellectual_disability": 1,
    "not_specified|not_provided|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 1,
    "Microphthalmia_with_brain_and_digit_anomalies|Orofacial_cleft_11|Absence_of_the_sacrum|Aplasia/hypoplasia_involving_bones_of_the_lower_limbs": 1,
    "not_provided|Microphthalmia_with_brain_and_digit_anomalies": 3,
    "Cleft_Lip_+/-_Cleft_Palate|_Autosomal_Dominant|Orofacial_cleft_11|Microphthalmia_with_brain_and_digit_anomalies": 1,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5": 148,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency": 197,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia": 3,
    "GTP_cyclohydrolase_I_deficiency|Dopa-responsive_dystonia": 4,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|not_provided": 13,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_provided": 15,
    "not_provided|GTP_cyclohydrolase_I_deficiency|Dystonia_5": 14,
    "not_provided|GTP_cyclohydrolase_I_deficiency|Dopa-responsive_dystonia": 1,
    "Dopa-responsive_dystonia|GTP_cyclohydrolase_I_deficiency|not_provided": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_specified|not_provided": 1,
    "Dopa-responsive_dystonia|GTP_cyclohydrolase_I_deficiency": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_provided|not_specified": 2,
    "Dystonia|_dopa-responsive|_with_or_without_hyperphenylalaninemia|_autosomal_recessive|not_specified": 1,
    "Dystonia_5": 24,
    "not_provided|Dystonia_5": 2,
    "not_specified|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 3,
    "Dystonia_5|Inborn_genetic_diseases": 1,
    "Dystonia|_dopa-responsive|_with_or_without_hyperphenylalaninemia|_autosomal_recessive|Dystonia_5|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|Inborn_genetic_diseases|Dopa-responsive_dystonia|GTP_cyclohydrolase_I_deficiency|not_provided": 1,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|Dystonia|_dopa-responsive|_with_or_without_hyperphenylalaninemia|_autosomal_recessive|not_specified|Intellectual_disability|not_provided": 1,
    "Rigidity|Gait_ataxia|Gait_imbalance|Sleep_abnormality|Muscle_weakness|Gait_disturbance": 1,
    "Dystonia_5|Inborn_genetic_diseases|GTP_cyclohydrolase_I_deficiency|not_provided": 1,
    "GTP_cyclohydrolase_I_deficiency": 2,
    "Dystonia_5|not_provided|GTP_cyclohydrolase_I_deficiency": 2,
    "not_specified|Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_provided": 1,
    "GTP_cyclohydrolase_I_deficiency|GCH1-related_disorder|not_provided|Dystonia_5": 1,
    "GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|Dystonia_5|GTP_cyclohydrolase_I_deficiency|Dopa-responsive_dystonia|not_specified|not_provided|Intellectual_disability": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|Inborn_genetic_diseases": 2,
    "Dystonia|_dopa-responsive|_with_or_without_hyperphenylalaninemia|_autosomal_recessive": 2,
    "not_provided|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 5,
    "GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|not_provided|GTP_cyclohydrolase_I_deficiency|Dystonia_5": 1,
    "Inborn_genetic_diseases|Dystonia_5|GTP_cyclohydrolase_I_deficiency|GCH1-related_disorder": 1,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|GCH1-related_disorder": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_provided|Intellectual_disability|not_specified": 1,
    "not_provided|GCH1-related_disorder|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 1,
    "Dystonic_disorder|Dystonia_5": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|GCH1-related_disorder": 1,
    "Dystonic_disorder|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 1,
    "GCH1-related_disorder|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 1,
    "GCH1-related_disorder|GTP_cyclohydrolase_I_deficiency|Dystonia_5": 1,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|Inborn_genetic_diseases": 2,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|GTP_cyclohydrolase_I_deficiency|not_provided": 1,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|Dystonia|_dopa-responsive|_with_or_without_hyperphenylalaninemia|_autosomal_recessive|not_provided": 1,
    "GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|6-Pyruvoyl-tetrahydrobiopterin_synthase_deficiency": 1,
    "not_provided|Abnormal_central_motor_function": 1,
    "GTP_cyclohydrolase_I_deficiency|Dystonia_5|not_specified|not_provided": 1,
    "GCH1-related_disorder|Hyperphenylalaninemia_due_to_tetrahydrobiopterin_deficiency|GTP_cyclohydrolase_I_deficiency|Dystonia_5|not_provided": 1,
    "Inborn_genetic_diseases|GTP_cyclohydrolase_I_deficiency|Dystonia_5": 1,
    "GCH1-related_disorder": 1,
    "not_provided|GCH1-related_disorder|GTP_cyclohydrolase_I_deficiency|Dystonia_5": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_specified|GCH1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Dystonia_5|GTP_cyclohydrolase_I_deficiency": 2,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia|GTP_cyclohydrolase_I_deficiency": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia": 1,
    "not_provided|Dystonia_5|GTP_cyclohydrolase_I_deficiency|not_specified": 1,
    "Dystonia_5|GTP_cyclohydrolase_I_deficiency|GTP_cyclohydrolase_I_deficiency_with_hyperphenylalaninemia": 1,
    "WDHD1-related_disorder": 1,
    "WDHD1-related_disorder|not_specified": 1,
    "not_specified|WDHD1-related_disorder": 1,
    "TMEM260-related_disorder": 9,
    "TMEM260-related_disorder|not_provided": 2,
    "Structural_heart_defects_and_renal_anomalies_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Structural_heart_defects_and_renal_anomalies_syndrome|not_provided": 1,
    "not_provided|TMEM260-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|TMEM260-related_disorder": 1,
    "not_provided|Structural_heart_defects_and_renal_anomalies_syndrome": 4,
    "Inborn_genetic_diseases|Structural_heart_defects_and_renal_anomalies_syndrome": 1,
    "not_provided|TMEM260-related_disorder|Structural_heart_defects_and_renal_anomalies_syndrome": 1,
    "Type_I_truncus_arteriosus|Structural_heart_defects_and_renal_anomalies_syndrome": 1,
    "Inborn_genetic_diseases|TMEM260-related_disorder": 1,
    "Structural_heart_defects_and_renal_anomalies_syndrome|Inborn_genetic_diseases": 1,
    "TMEM260-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Pituitary_hormone_deficiency|_combined|_6|Syndromic_microphthalmia_type_5": 9,
    "OTX2-Related_Syndromic_Microphthalmia|Retinal_dystrophy|Syndromic_Microphthalmia|_Dominant|Pituitary_hormone_deficiency|_combined|_6": 2,
    "Syndromic_microphthalmia_type_5|Syndromic_Microphthalmia|_Dominant|Retinal_dystrophy|Pituitary_hormone_deficiency|_combined|_6": 3,
    "Syndromic_microphthalmia_type_5|OTX2-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Pituitary_hormone_deficiency|_combined|_6": 2,
    "Syndromic_microphthalmia_type_5|OTX2-Related_Syndromic_Microphthalmia|Retinal_dystrophy|Pituitary_hormone_deficiency|_combined|_6": 2,
    "Retinal_dystrophy|OTX2-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Combined_Pituitary_Hormone_Deficiency|_Dominant": 2,
    "OTX2-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Retinal_dystrophy|Combined_Pituitary_Hormone_Deficiency|_Dominant|not_provided": 1,
    "Syndromic_microphthalmia_type_5|Pituitary_hormone_deficiency|_combined|_6|OTX2-Related_Syndromic_Microphthalmia|not_specified|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Anophthalmia-microphthalmia_syndrome": 4,
    "Pituitary_hormone_deficiency|_combined|_6|Anophthalmia-microphthalmia_syndrome": 2,
    "not_provided|not_specified|Anophthalmia-microphthalmia_syndrome": 2,
    "Syndromic_microphthalmia_type_5": 19,
    "Anophthalmia-microphthalmia_syndrome|Microcephaly": 1,
    "Inborn_genetic_diseases|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "Pituitary_hormone_deficiency|_combined|_6": 4,
    "Pituitary_hormone_deficiency|_combined|_6|not_specified|Anophthalmia-microphthalmia_syndrome|not_provided|Syndromic_microphthalmia_type_5": 1,
    "Anophthalmia-microphthalmia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Anophthalmia-microphthalmia_syndrome|Inborn_genetic_diseases": 4,
    "Anophthalmia-microphthalmia_syndrome|not_specified|not_provided": 1,
    "Syndromic_microphthalmia_type_5|Anophthalmia-microphthalmia_syndrome|Pituitary_hormone_deficiency|_combined|_6|Inborn_genetic_diseases|not_provided": 1,
    "Syndromic_microphthalmia_type_5|not_provided|OTX2-related_disorder": 1,
    "Syndromic_microphthalmia_type_5|Anophthalmia-microphthalmia_syndrome": 1,
    "OTX2-related_disorder": 6,
    "OTX2-related_disorder|Anophthalmia-microphthalmia_syndrome": 1,
    "Syndromic_microphthalmia_type_5|OTX2-Related_Syndromic_Microphthalmia|Syndromic_Microphthalmia|_Dominant|Pituitary_hormone_deficiency|_combined|_6|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|Anophthalmia-microphthalmia_syndrome|Syndromic_microphthalmia_type_5": 1,
    "Anophthalmia-microphthalmia_syndrome|Pituitary_hormone_deficiency|_combined|_6|Syndromic_microphthalmia_type_5|Retinal_dystrophy|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|46|XY_partial_gonadal_dysgenesis|not_provided": 1,
    "OTX2-Related_Syndromic_Microphthalmia": 1,
    "Syndromic_microphthalmia_type_5|Syndromic_Microphthalmia|_Dominant|OTX2-Related_Syndromic_Microphthalmia|Inborn_genetic_diseases|Pituitary_hormone_deficiency|_combined|_6|Anophthalmia-microphthalmia_syndrome": 1,
    "Syndromic_microphthalmia_type_5|OTX2-Related_Syndromic_Microphthalmia|OTX2-related_disorder|Retinal_dystrophy|Pituitary_hormone_deficiency|_combined|_6|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|Anophthalmia-microphthalmia_syndrome|Syndromic_microphthalmia_type_5|Pituitary_hormone_deficiency|_combined|_6": 1,
    "not_provided|Syndromic_microphthalmia_type_5": 2,
    "Syndromic_Microphthalmia|_Dominant|OTX2-Related_Syndromic_Microphthalmia|Retinal_dystrophy|Pituitary_hormone_deficiency|_combined|_6|Anophthalmia-microphthalmia_syndrome": 2,
    "Nystagmus|Hypertonia|Low-set_ears|Hypotelorism|Protruding_ear|Pointed_chin|Phonophobia|Horizontal_nystagmus|Anxiety": 1,
    "Anophthalmia-microphthalmia_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|OTX2-related_disorder": 1,
    "Syndromic_microphthalmia_type_5|OTX2-Related_Syndromic_Microphthalmia|Retinal_dystrophy|Pituitary_hormone_deficiency|_combined|_6|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "not_provided|Retinal_dystrophy|Syndromic_Microphthalmia|_Dominant|OTX2-Related_Syndromic_Microphthalmia|Combined_Pituitary_Hormone_Deficiency|_Dominant": 1,
    "Lethal_multiystemic_syndrome": 1,
    "PROTEASOME-ASSOCIATED_AUTOINFLAMMATORY_SYNDROME_1|_DIGENIC": 2,
    "not_provided|PSMA3-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|not_provided": 21,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23": 320,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|not_provided": 34,
    "KIAA0586-related_disorder": 10,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 654,
    "KIAA0586-related_disorder|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23": 7,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|not_provided|KIAA0586-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Primary_ciliary_dyskinesia": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23": 16,
    "not_provided|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|Inborn_genetic_diseases": 4,
    "KIAA0586-related_disorder|Neurodevelopmental_disorder|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|Retinal_dystrophy|not_provided|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|Inborn_genetic_diseases": 32,
    "KIAA0586-related_disorder|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome_23|not_provided": 3,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Inborn_genetic_diseases|not_provided|KIAA0586-related_disorder": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Inborn_genetic_diseases": 23,
    "not_provided|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23": 11,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|Inborn_genetic_diseases|not_provided": 6,
    "Joubert_syndrome_23": 15,
    "Joubert_syndrome_23|not_provided|Short-rib_thoracic_dysplasia_14_with_polydactyly": 3,
    "KIAA0586-related_disorder|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 8,
    "not_provided|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Inborn_genetic_diseases": 2,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|KIAA0586-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Joubert_syndrome_and_related_disorders|KIAA0586-_Related_disorders|KIAA0586-related_disorder|Congenital_cerebellar_hypoplasia|Intellectual_disability|Rod-cone_dystrophy|Joubert_syndrome": 1,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 27,
    "Inborn_genetic_diseases|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 11,
    "not_provided|Joubert_syndrome_23": 1,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|KIAA0586-related_disorder": 5,
    "not_specified|not_provided|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|Inborn_genetic_diseases|KIAA0586-related_disorder": 1,
    "Joubert_syndrome_23|Neurodevelopmental_disorder|Short-rib_thoracic_dysplasia_14_with_polydactyly|Intellectual_disability|Rod-cone_dystrophy|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 5,
    "KIAA0586-related_disorder|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|not_provided": 1,
    "Joubert_syndrome_23|KIAA0586-related_disorder|not_provided": 1,
    "KIAA0586-_Related_disorders": 1,
    "Joubert_syndrome_23|not_provided|Short-rib_thoracic_dysplasia_14_with_polydactyly|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|Inborn_genetic_diseases|not_provided": 2,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|not_provided|Joubert_syndrome_23": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 4,
    "KIAA0586-related_disorder|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|Inborn_genetic_diseases": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|KIAA0586-related_disorder": 3,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|not_provided|Joubert_syndrome_and_related_disorders": 1,
    "not_provided|Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23": 2,
    "Joubert_syndrome|Joubert_syndrome_23": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|not_specified": 1,
    "not_provided|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|KIAA0586-related_disorder": 1,
    "not_provided|KIAA0586-related_disorder": 1,
    "not_provided|Joubert_syndrome_23|not_specified|KIAA0586-related_disorder|Short-rib_thoracic_dysplasia_14_with_polydactyly": 1,
    "not_provided|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|KIAA0586-related_disorder": 1,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|KIAA0586-related_disorder|not_provided|not_specified": 1,
    "not_provided|KIAA0586-related_disorder|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 2,
    "Inborn_genetic_diseases|not_provided|KIAA0586-related_disorder|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly": 1,
    "Joubert_syndrome_23|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|not_provided|not_specified": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|not_provided|KIAA0586-related_disorder": 1,
    "not_provided|Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|KIAA0586-related_disorder|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_23|Short-rib_thoracic_dysplasia_14_with_polydactyly|KIAA0586-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_23|not_provided|KIAA0586-related_disorder|Short-rib_thoracic_dysplasia_14_with_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|not_specified": 1,
    "KIAA0586-related_disorder|Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|not_provided": 2,
    "Short-rib_thoracic_dysplasia_14_with_polydactyly|Joubert_syndrome_23|KIAA0586-related_disorder|not_provided": 1,
    "DACT1-related_disorder": 12,
    "DACT1-related_disorder|not_provided": 7,
    "Townes-Brocks_syndrome_2|not_provided": 3,
    "Townes-Brocks_syndrome_2": 10,
    "not_provided|Townes-Brocks_syndrome_2": 1,
    "not_specified|DACT1-related_disorder|Townes_syndrome|not_provided": 1,
    "DACT1-related_neural_tube_defects": 1,
    "Townes_syndrome|not_specified": 3,
    "Townes-Brocks_syndrome_2|not_specified|not_provided": 1,
    "not_specified|Townes-Brocks_syndrome_2": 1,
    "DACT1-related_disorder|not_provided|not_specified": 1,
    "not_provided|DACT1-related_disorder": 1,
    "DAAM1-related_disorder": 9,
    "DAAM1-related_disorder|not_provided": 4,
    "not_provided|DAAM1-related_disorder": 2,
    "JKAMP_neurodevelopmental_disorder": 8,
    "JKAMP-related_neurodevelopmental_disorder": 1,
    "C14orf39-related_disorder|not_provided": 1,
    "Spermatogenic_failure_52|Non-obstructive_azoospermia": 2,
    "Spermatogenic_failure_52|Premature_ovarian_failure_18": 1,
    "Non-obstructive_azoospermia|Spermatogenic_failure_52|Premature_ovarian_failure_18|Azoospermia": 1,
    "Spermatogenic_failure_52": 1,
    "Developmental_cataract|Cornea_plana|Microphthalmia|Sclerocornea": 1,
    "Colobomatous_optic_disc-macular_atrophy-chorioretinopathy_syndrome": 6,
    "Anophthalmia-microphthalmia_syndrome|SIX6-related_disorder|not_provided|Colobomatous_optic_disc-macular_atrophy-chorioretinopathy_syndrome|Anophthalmia/microphthalmia-esophageal_atresia_syndrome": 1,
    "Colobomatous_optic_disc-macular_atrophy-chorioretinopathy_syndrome|Anophthalmia-microphthalmia_syndrome|not_provided|not_specified": 1,
    "not_provided|Colobomatous_optic_disc-macular_atrophy-chorioretinopathy_syndrome": 1,
    "Nystagmus|Microcornea|Developmental_cataract|Sclerocornea": 1,
    "not_specified|Colobomatous_optic_disc-macular_atrophy-chorioretinopathy_syndrome|Anophthalmia-microphthalmia_syndrome|not_provided": 1,
    "Colobomatous_optic_disc-macular_atrophy-chorioretinopathy_syndrome|Anophthalmia/microphthalmia-esophageal_atresia_syndrome|not_provided|Anophthalmia-microphthalmia_syndrome": 1,
    "SIX6-related_disorder|not_provided": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|Branchiootorenal_Spectrum_Disorders": 7,
    "Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23": 59,
    "Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 50,
    "Branchiootorenal_Spectrum_Disorders|Nonsyndromic_Hearing_Loss|_Dominant": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3|not_provided": 6,
    "Branchiootorenal_Spectrum_Disorders|not_provided|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "not_provided|Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23": 6,
    "Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|not_provided": 11,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 2,
    "Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootorenal_syndrome_1": 1,
    "Inborn_genetic_diseases|Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23": 3,
    "Branchiootic_syndrome_3|not_provided|SIX1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootorenal_syndrome_1": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 1,
    "Branchiootic_syndrome_3": 15,
    "Autosomal_dominant_nonsyndromic_hearing_loss_23": 6,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3|Branchiootorenal_syndrome_1|not_provided|SIX1-related_disorder": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 1,
    "Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|SIX1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_23|not_provided": 1,
    "not_provided|Unilateral_deafness": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 1,
    "not_provided|Branchiootic_syndrome_3": 1,
    "Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|Inborn_genetic_diseases": 1,
    "Branchiootorenal_syndrome_1|Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23": 1,
    "SIX1-related_disorder|Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome|not_provided|Branchiootorenal_syndrome_1": 1,
    "Branchiootic_syndrome_1|Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|not_specified": 1,
    "SIX1-related_disorder": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3|not_provided|SIX1-related_disorder": 1,
    "Branchiootic_syndrome_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hearing_impairment|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootic_syndrome_3": 1,
    "Branchiootic_syndrome_3|Autosomal_dominant_nonsyndromic_hearing_loss_23|Branchiootorenal_syndrome_1|not_specified|not_provided": 1,
    "not_provided|not_specified|SIX1-related_disorder": 1,
    "SIX4-related_disorder": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_26": 5,
    "Intellectual_disability|TRMT5-related_disorder|Combined_oxidative_phosphorylation_defect_type_26|not_provided": 1,
    "TRMT5-related_disorder": 6,
    "not_provided|TRMT5-related_disorder": 7,
    "Combined_oxidative_phosphorylation_defect_type_26": 5,
    "Inborn_genetic_diseases|TRMT5-related_disorder|not_provided": 1,
    "TRMT5-related_disorder|not_provided": 4,
    "not_specified|TRMT5-related_disorder|not_provided": 1,
    "TRMT5-related_disorder|Combined_oxidative_phosphorylation_defect_type_26|not_specified|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_26|Inborn_genetic_diseases|not_provided|TRMT5-related_disorder": 1,
    "Ischemic_stroke": 1,
    "Cerebral_infarction|_susceptibility_to": 1,
    "PRKCH-related_disorder": 1,
    "Maffucci_syndrome|not_provided": 1,
    "Enchondromatosis|not_provided": 1,
    "Cholangiocarcinoma|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy_112": 2,
    "KCNH5-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 3,
    "Developmental_and_epileptic_encephalopathy|KCNH5-related_disorder": 1,
    "Metabolic_crises|_recurrent|_with_variable_encephalomyopathic_features_and_neurologic_regression": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12": 40,
    "Developmental_and_epileptic_encephalopathy_112": 5,
    "not_specified|KCNH5-related_disorder|Developmental_and_epileptic_encephalopathy": 2,
    "KCNH5-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Developmental_and_epileptic_encephalopathy_112|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Developmental_and_epileptic_encephalopathy_112|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|KCNH5-related_disorder": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 139,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2689,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|SYNE2-related_disorder": 10,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified": 229,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 204,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided": 70,
    "not_provided|SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 5,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided|not_specified": 19,
    "not_provided|not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 28,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified": 17,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified|not_provided": 22,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided": 29,
    "SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 14,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|SYNE2-related_disorder": 3,
    "SYNE2-related_disorder": 21,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 60,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified|not_provided|SYNE2-related_disorder": 2,
    "SYNE2-related_disorder|not_provided|not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 3,
    "SYNE2-related_disorder|not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2,
    "See_cases|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 1,
    "not_provided|not_specified|SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided|SYNE2-related_disorder": 5,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|SYNE2-related_disorder|not_provided": 3,
    "Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified": 2,
    "SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided": 7,
    "SYNE2-related_disorder|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 17,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided|SYNE2-related_disorder|not_specified": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|SYNE2-related_disorder|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified|SYNE2-related_disorder": 2,
    "not_specified|SYNE2-related_disorder": 1,
    "SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified": 7,
    "SYNE2-related_disorder|not_specified": 1,
    "not_provided|SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided|SYNE2-related_disorder": 1,
    "not_specified|SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|SYNE2-related_disorder": 2,
    "not_specified|SYNE2-related_disorder|not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 1,
    "not_specified|not_provided|SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified|SYNE2-related_disorder": 1,
    "not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 1,
    "not_provided|SYNE2-related_disorder|not_specified|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2,
    "SYNE2-related_disorder|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_provided|not_specified": 2,
    "SYNE2-related_disorder|not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 4,
    "Spastic_ataxia|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 2,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|not_specified|SYNE2-related_disorder|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant": 1,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_5|_autosomal_dominant|Restrictive_cardiomyopathy|Long_QT_syndrome": 1,
    "not_provided|ESR2-related_disorder": 9,
    "ESR2-related_disorder|not_provided": 7,
    "ESR2-related_disorder|not_specified": 1,
    "not_specified|Ovarian_dysgenesis_8": 1,
    "Ovarian_dysgenesis_8": 2,
    "ESR2-related_disorder": 1,
    "MTHFD1-related_disorder|not_provided": 6,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|Neural_tube_defects|_folate-sensitive": 5,
    "Severe_combined_immunodeficiency_disease|not_provided|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|Neural_tube_defects|_folate-sensitive": 1,
    "Neural_tube_defects|_folate-sensitive|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_provided": 4,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia": 7,
    "not_provided|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia": 3,
    "not_provided|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_specified": 1,
    "not_provided|MTHFD1-related_disorder": 6,
    "MTHFD1-related_disorder": 5,
    "Severe_combined_immunodeficiency_disease|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_provided": 1,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_provided|Neural_tube_defects|_folate-sensitive": 1,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_provided": 3,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_specified|Spina_bifida|_folate-sensitive|_susceptibility_to|not_provided": 1,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|Neural_tube_defects|_folate-sensitive|not_provided": 3,
    "Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_specified": 1,
    "Neural_tube_defects|_folate-sensitive|_susceptibility_to|not_specified|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Combined_immunodeficiency_and_megaloblastic_anemia_with_or_without_hyperhomocysteinemia": 1,
    "ZBTB25-related_disorder": 5,
    "not_specified|ZBTB25-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spherocytosis_type_2": 1,
    "SPTB-related_disorder|not_provided": 16,
    "SPTB-related_disorder": 42,
    "Hereditary_spherocytosis_type_2": 75,
    "SPTB-related_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Hereditary_spherocytosis_type_2|Elliptocytosis_3|not_provided": 2,
    "Elliptocytosis|Spherocytosis|_Dominant|not_provided": 10,
    "Elliptocytosis|Spherocytosis|_Dominant": 27,
    "Spherocytosis|_Dominant|Elliptocytosis|not_provided": 2,
    "Spherocytosis|_Dominant|not_provided|Elliptocytosis": 5,
    "not_provided|Elliptocytosis|not_specified|Spherocytosis|_Dominant": 6,
    "Elliptocytosis_3": 9,
    "not_provided|Elliptocytosis|Spherocytosis|_Dominant": 18,
    "Elliptocytosis_3|not_provided": 1,
    "not_provided|Elliptocytosis_3": 1,
    "SPTB-related_disorder|ANEMIA|_PERINATAL_HEMOLYTIC|_FATAL_OR_NEAR-FATAL|not_provided|Hereditary_spherocytosis_type_2": 1,
    "SPTB-related_disorder|Hereditary_spherocytosis_type_2|not_provided": 1,
    "SPTB-related_disorder|not_provided|Elliptocytosis_3|Hereditary_spherocytosis_type_2": 1,
    "Elliptocytosis_3|Pyropoikilocytosis|_hereditary": 1,
    "not_specified|Elliptocytosis|not_provided|Spherocytosis|_Dominant": 2,
    "Hereditary_spherocytosis_type_2|not_provided": 14,
    "not_provided|Spherocytosis|_Dominant|not_specified|Elliptocytosis": 3,
    "not_provided|Elliptocytosis|Spherocytosis|_Dominant|Elliptocytosis_3": 1,
    "not_provided|Inborn_genetic_diseases|Elliptocytosis_3|Hereditary_spherocytosis_type_2": 1,
    "not_provided|SPTB-related_disorder": 8,
    "not_provided|Elliptocytosis|Spherocytosis|_Dominant|Inborn_genetic_diseases": 3,
    "not_specified|Elliptocytosis|Spherocytosis|_Dominant|not_provided": 1,
    "SPTB-related_disorder|not_provided|Elliptocytosis_3": 1,
    "not_provided|Hereditary_spherocytosis_type_2": 19,
    "Elliptocytosis|not_provided|Spherocytosis|_Dominant": 8,
    "not_provided|not_specified|Elliptocytosis|Spherocytosis|_Dominant|Inborn_genetic_diseases": 1,
    "Elliptocytosis|not_provided|Spherocytosis|_Dominant|SPTB-related_disorder": 1,
    "Elliptocytosis|Inborn_genetic_diseases|Spherocytosis|_Dominant": 2,
    "Elliptocytosis_3|Hereditary_spherocytosis_type_2|not_provided": 2,
    "not_provided|SPTB-related_disorder|Hereditary_spherocytosis_type_2": 1,
    "not_provided|Elliptocytosis|not_specified|Hereditary_spherocytosis_type_2|Spherocytosis|_Dominant": 4,
    "Elliptocytosis|SPTB-related_disorder|not_provided|Spherocytosis|_Dominant|Hereditary_spherocytosis_type_2": 1,
    "Elliptocytosis|not_provided|not_specified|Spherocytosis|_Dominant": 2,
    "not_provided|not_specified|Elliptocytosis|Spherocytosis|_Dominant": 3,
    "Elliptocytosis|not_specified|Hereditary_spherocytosis_type_2|not_provided|Spherocytosis|_Dominant": 1,
    "Elliptocytosis_3|Hereditary_spherocytosis_type_2": 4,
    "Elliptocytosis|not_specified|Spherocytosis|_Dominant|not_provided": 2,
    "not_specified|Elliptocytosis|not_provided|Hereditary_spherocytosis_type_2|Spherocytosis|_Dominant": 1,
    "Hereditary_spherocytosis|Spherocytosis|Elliptocytosis_3": 1,
    "Elliptocytosis|Inborn_genetic_diseases|not_provided|Spherocytosis|_Dominant|SPTB-related_disorder": 1,
    "Elliptocytosis|Hereditary_spherocytosis_type_2|not_specified|Spherocytosis|_Dominant|not_provided": 1,
    "not_specified|Elliptocytosis|Hereditary_spherocytosis_type_2|not_provided|Spherocytosis|_Dominant": 1,
    "not_provided|Elliptocytosis_3|Hereditary_spherocytosis_type_2": 3,
    "not_specified|Elliptocytosis|Hereditary_spherocytosis_type_2|Spherocytosis|_Dominant|not_provided": 1,
    "Chudley-McCullough_syndrome|not_provided|Hereditary_spherocytosis_type_2": 1,
    "Hereditary_spherocytosis_type_2|not_specified|not_provided": 1,
    "Spherocytosis|_Dominant|not_specified|Elliptocytosis|not_provided": 1,
    "Hereditary_spherocytosis_type_2|Elliptocytosis_3": 3,
    "Hereditary_spherocytosis_type_2|Elliptocytosis_3|Inborn_genetic_diseases": 1,
    "Spherocytosis|_Dominant|Elliptocytosis|Inborn_genetic_diseases": 2,
    "not_provided|Elliptocytosis|Spherocytosis|_Dominant|SPTB-related_disorder": 2,
    "not_provided|not_specified|Elliptocytosis|Hereditary_spherocytosis_type_2|Spherocytosis|_Dominant": 2,
    "Elliptocytosis|Inborn_genetic_diseases|not_provided|Spherocytosis|_Dominant": 1,
    "Inborn_genetic_diseases|not_provided|SPTB-related_disorder": 1,
    "not_provided|Hereditary_spherocytosis_type_2|Elliptocytosis_3": 2,
    "Hereditary_spherocytosis_type_2|Inborn_genetic_diseases": 1,
    "SPTB-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_2|Elliptocytosis_3": 1,
    "not_specified|not_provided|Hereditary_spherocytosis_type_2": 1,
    "Elliptocytosis|not_provided|Spherocytosis|_Dominant|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Elliptocytosis|Spherocytosis|_Dominant": 1,
    "Elliptocytosis|not_specified|not_provided|Spherocytosis|_Dominant": 1,
    "Anemia": 1,
    "not_provided|Elliptocytosis|Elliptocytosis_3|Hereditary_spherocytosis_type_2|Spherocytosis|_Dominant": 1,
    "not_provided|Elliptocytosis|Spherocytosis|_Dominant|Inborn_genetic_diseases|SPTB-related_disorder": 2,
    "Hereditary_spherocytosis_type_2|not_provided|Elliptocytosis_3|Inborn_genetic_diseases": 1,
    "not_specified|Spherocytosis|_Dominant|not_provided|Elliptocytosis": 1,
    "Pyropoikilocytosis|_hereditary|SPTB-related_disorder|not_provided|Elliptocytosis|Spherocytosis|_Dominant": 1,
    "not_provided|Elliptocytosis|Hereditary_spherocytosis_type_2|Spherocytosis|_Dominant": 1,
    "Elliptocytosis|Hereditary_spherocytosis_type_2|not_specified|not_provided|Spherocytosis|_Dominant": 1,
    "Elliptocytosis_3|Hereditary_spherocytosis_type_2|SPTB-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Elliptocytosis|Spherocytosis|_Dominant": 1,
    "Elliptocytosis|Spherocytosis|_Dominant|not_provided|Elliptocytosis_3": 1,
    "not_specified|Hereditary_spherocytosis_type_2|not_provided": 1,
    "not_provided|Pheochromocytoma|MAX-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Pheochromocytoma|not_provided": 1,
    "MAX-related_disorder": 4,
    "not_specified|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_provided|MAX-related_disorder": 1,
    "Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Polydactyly-macrocephaly_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Retinoblastoma|Pheochromocytoma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Polydactyly-macrocephaly_syndrome|Pheochromocytoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome|MAX-related_disorder": 1,
    "Pheochromocytoma|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma|Polydactyly-macrocephaly_syndrome|MAX-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 1,
    "not_provided|Polydactyly-macrocephaly_syndrome|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Pheochromocytoma|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|_susceptibility_to|not_provided": 1,
    "Pheochromocytoma|_susceptibility_to": 1,
    "not_provided|Hereditary_pheochromocytoma-paraganglioma|Polydactyly-macrocephaly_syndrome|MAX-related_disorder|MAX-associated_Macrocephaly_and_Polydactyly_syndrome": 1,
    "MAX-related_disorder|Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma": 1,
    "Pheochromocytoma|Polydactyly-macrocephaly_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|MAX-related_disorder|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Hereditary_pheochromocytoma-paraganglioma|Pheochromocytoma|Pheochromocytoma|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "MAX-related_disorder|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|Hereditary_pheochromocytoma-paraganglioma|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_pheochromocytoma-paraganglioma|not_provided|Pheochromocytoma": 1,
    "not_specified|not_provided|Hereditary_pheochromocytoma-paraganglioma": 2,
    "Hereditary_pheochromocytoma-paraganglioma|not_specified|Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pheochromocytoma|_susceptibility_to": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_1": 7,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation_with_defective_fucosylation_1": 2,
    "not_provided|FUT8-related_disorder|Congenital_disorder_of_glycosylation_with_defective_fucosylation_1|not_specified": 1,
    "FUT8-related_disorder": 11,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_1|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|FUT8-related_disorder": 4,
    "not_provided|FUT8-related_disorder|not_specified": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_1|not_provided|FUT8-related_disorder": 1,
    "not_provided|Congenital_disorder_of_glycosylation_with_defective_fucosylation_1|FUT8-related_disorder": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_1|not_provided": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 639,
    "Inborn_genetic_diseases|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 7,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|not_provided|GPHN-related_disorder": 1,
    "Inborn_genetic_diseases|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|Hyperekplexia_1|not_provided|Hyperekplexia": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|Inborn_genetic_diseases": 18,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|not_provided|not_specified": 2,
    "Seizure|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 1,
    "Inborn_genetic_diseases|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|not_provided": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|not_provided|Hyperekplexia_1": 1,
    "not_provided|not_specified|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 14,
    "Inborn_genetic_diseases|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_A|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|Hyperekplexia_1|GPHN-related_disorder": 1,
    "Inborn_genetic_diseases|Hyperekplexia_1|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|not_provided": 6,
    "GPHN-related_disorder|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 4,
    "GPHN-related_disorder": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|Dementia": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|GPHN-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|Hyperekplexia_1|not_provided": 1,
    "not_specified|Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C": 1,
    "Sulfite_oxidase_deficiency_due_to_molybdenum_cofactor_deficiency_type_C|GPHN-related_disorder|not_provided": 1,
    "Atypical_Rett_syndrome": 2,
    "PALS1-related_disorder": 4,
    "Anxiety|Abnormal_facial_shape|Arachnoid_cyst|Cerebral_palsy|Intellectual_disability": 1,
    "not_provided|PIGH-related_disorder|Glycosylphosphatidylinositol_biosynthesis_defect_17|Inborn_genetic_diseases": 1,
    "not_specified|PIGH-related_disorder|not_provided": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_17": 2,
    "PIGH-related_disorder": 4,
    "PIGH-related_disorder|not_provided": 1,
    "RDH11-related_disorder|not_provided": 3,
    "Retinitis_pigmentosa-juvenile_cataract-short_stature-intellectual_disability_syndrome|not_provided": 3,
    "Retinitis_pigmentosa-juvenile_cataract-short_stature-intellectual_disability_syndrome": 2,
    "not_provided|RDH11-related_disorder": 3,
    "RDH11-related_disorder": 1,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive": 5,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa": 4,
    "RDH12-related_disorder": 3,
    "Leber_congenital_amaurosis_13": 400,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 23,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis_13|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_13|Leber_congenital_amaurosis": 26,
    "Retinal_dystrophy|Leber_congenital_amaurosis_13": 8,
    "Leber_congenital_amaurosis_13|not_provided|not_specified": 1,
    "RDH12-related_disorder|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Leber_congenital_amaurosis|RDH12-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_13|Inborn_genetic_diseases": 2,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|not_provided": 5,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Cone-rod_dystrophy|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Retinitis_pigmentosa": 3,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 2,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "Macular_dystrophy|not_specified|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "not_provided|Leber_congenital_amaurosis_13": 3,
    "Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive|Optic_atrophy|Leber_congenital_amaurosis_13|not_specified": 1,
    "Leber_congenital_amaurosis_13|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_13|Retinal_dystrophy": 4,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Leber_congenital_amaurosis_13|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_13|not_specified": 1,
    "Leber_congenital_amaurosis_13|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_13|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis_13|Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_13": 1,
    "not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_13|Leber_congenital_amaurosis|RDH12-related_disorder": 1,
    "Leber_congenital_amaurosis_13|Autosomal_dominant_retinitis_pigmentosa|RDH12-related_disorder|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|not_provided|Leber_congenital_amaurosis_13": 2,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis|RDH12-related_disorder|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Retinitis_pigmentosa_53|Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis|not_provided|RDH12-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_13": 2,
    "not_specified|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Retinal_dystrophy|Macular_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_13": 2,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Cone-rod_dystrophy|Leber_congenital_amaurosis_13|See_cases": 1,
    "Cone-rod_dystrophy|Retinal_dystrophy|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "Retinal_dystrophy|not_specified|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_13|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis_13|not_provided|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_13|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_13": 4,
    "RDH12-related_disorder|Leber_congenital_amaurosis_13|Leber_congenital_amaurosis|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis_13|Retinitis_pigmentosa|Retinal_dystrophy": 2,
    "Macular_dystrophy|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|RDH12-related_disorder|Macular_dystrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_13": 2,
    "Leber_congenital_amaurosis_13|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|Retinitis_pigmentosa|Inborn_genetic_diseases|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis_13|not_specified|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_13|Macular_dystrophy": 2,
    "Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Macular_dystrophy|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Leber_congenital_amaurosis|not_provided": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Leber_congenital_amaurosis": 1,
    "Abnormality_of_the_eye|Retinitis_pigmentosa|Leber_congenital_amaurosis_13": 1,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_13|Inborn_genetic_diseases|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_13|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_53|Leber_congenital_amaurosis_13|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_13|Retinal_dystrophy": 1,
    "RDH12-related_disorder|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Leber_congenital_amaurosis_13|Abnormality_of_the_eye": 1,
    "Macular_dystrophy_with_or_without_cone_dysfunction|Leber_congenital_amaurosis|Retinal_dystrophy|Leber_congenital_amaurosis_13": 1,
    "Leber_congenital_amaurosis_13|Leber_congenital_amaurosis|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis_13|Leber_congenital_amaurosis|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_13|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Hereditary_spastic_paraplegia_15": 229,
    "Hereditary_spastic_paraplegia_15|not_provided": 13,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|Hereditary_spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia_15": 4,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 3,
    "ZFYVE26-related_disorder|Spastic_paraplegia": 9,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 36,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases": 2,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15|not_specified": 2,
    "Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases|Spastic_paraplegia": 6,
    "Hereditary_spastic_paraplegia_15|not_provided|Spastic_paraplegia": 3,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 42,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Retinal_dystrophy|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 4,
    "Spastic_paraplegia|ZFYVE26-related_disorder|Hereditary_spastic_paraplegia_15": 1,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia": 3,
    "not_specified|Hereditary_spastic_paraplegia_15|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|not_provided": 6,
    "Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 4,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_15": 4,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15": 8,
    "Spastic_paraplegia|ZFYVE26-related_disorder": 3,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_15|not_provided": 5,
    "Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia": 3,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 6,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|not_provided": 1,
    "Tip-toe_gait|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|Inborn_genetic_diseases|ZFYVE26-related_disorder": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_15": 1,
    "ZFYVE26-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia_15|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_15|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 3,
    "Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 1,
    "not_provided|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 5,
    "not_specified|Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_provided": 3,
    "not_specified|ZFYVE26-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Spastic_Paraplegia|_Recessive": 1,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 2,
    "Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia_15": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "ZFYVE26-related_disorder|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia|not_specified": 1,
    "Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_15": 3,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|ZFYVE26-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_15|Atypical_behavior|Intellectual_disability|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 2,
    "Spastic_paraplegia|Inborn_genetic_diseases|Spastic_Paraplegia|_Recessive|not_specified": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 1,
    "ZFYVE26-related_disorder|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "ZFYVE26-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "not_provided|Hereditary_spastic_paraplegia_15|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "ZFYVE26-related_disorder": 2,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_15": 1,
    "Spastic_paraplegia|Spastic_Paraplegia|_Recessive|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|not_provided": 1,
    "Hereditary_spastic_paraplegia_15|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_15|not_specified|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_15": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_15|not_provided": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified": 4,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Tip-toe_gait": 1,
    "Hereditary_spastic_paraplegia_15|ZFYVE26-related_disorder|Spastic_paraplegia|not_specified": 1,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|Spastic_Paraplegia|_Recessive|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 1,
    "Spastic_paraplegia|ZFYVE26-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|Hereditary_spastic_paraplegia_15|not_provided|not_specified": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia_15|ZFYVE26-related_disorder|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_15": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_15|not_provided|Spastic_paraplegia": 1,
    "ZFYVE26-related_disorder|Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia_15|Congenital_myopathy|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases": 1,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia_15": 2,
    "ZFYVE26-related_disorder|Hereditary_spastic_paraplegia_15|Inborn_genetic_diseases|not_specified|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_15|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|Tip-toe_gait|ZFYVE26-related_disorder|not_specified": 1,
    "Hereditary_spastic_paraplegia_15|Spastic_paraplegia|Inborn_genetic_diseases": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|ZFYVE26-related_disorder": 1,
    "ZFYVE26-related_disorder|Spastic_paraplegia|not_provided": 1,
    "ZFYVE26-related_disorder|Spastic_paraplegia|Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_15": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_15|Spastic_paraplegia": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_15|not_specified|Hereditary_spastic_paraplegia": 1,
    "RAD51B-related_disorder": 14,
    "not_provided|RAD51B-related_disorder": 3,
    "RAD51B-related_disorder|not_provided": 3,
    "RAD51B-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_specified|not_provided|RAD51B-related_disorder": 1,
    "not_specified|RAD51B-related_disorder": 1,
    "Hereditary_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|RAD51B-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Poly_(ADP-Ribose)_polymerase_inhibitor_response|not_provided": 1,
    "ACTN1-related_disorder": 12,
    "Abnormal_bleeding|Thrombocytopenia|Platelet-type_bleeding_disorder_15": 1,
    "Platelet-type_bleeding_disorder_15": 29,
    "ACTN1-related_disorder|not_provided": 15,
    "Platelet-type_bleeding_disorder_15|not_provided": 7,
    "not_provided|ACTN1-related_disorder": 5,
    "not_provided|Platelet-type_bleeding_disorder_15": 6,
    "not_specified|Platelet-type_bleeding_disorder_15|not_provided": 1,
    "Platelet-type_bleeding_disorder_15|ACTN1-related_disorder": 1,
    "not_provided|Macrothrombocytopenia|Platelet-type_bleeding_disorder_15": 2,
    "Platelet-type_bleeding_disorder_15|Macrothrombocytopenia": 1,
    "Platelet-type_bleeding_disorder_15|Inborn_genetic_diseases": 2,
    "Macrothrombocytopenia|Thrombocytopenia": 2,
    "ACTN1-related_disorder|Macrothrombocytopenia|Platelet-type_bleeding_disorder_15": 1,
    "Inborn_genetic_diseases|Platelet-type_bleeding_disorder_15|not_provided": 1,
    "Macrothrombocytopenia|Platelet-type_bleeding_disorder_15": 1,
    "Inborn_genetic_diseases|ACTN1-related_disorder": 1,
    "Macrothrombocytopenia|not_provided": 1,
    "ACTN1-related_disorder|Platelet-type_bleeding_disorder_15": 1,
    "ACTN1-related_disorder|Platelet-type_bleeding_disorder_15|Inborn_genetic_diseases|not_provided": 1,
    "Macrothrombocytopenia|Platelet-type_bleeding_disorder_15|Thrombocytopenia": 1,
    "Macrothrombocytopenia|not_provided|Platelet-type_bleeding_disorder_15": 2,
    "Platelet-type_bleeding_disorder_15|not_specified|not_provided": 1,
    "not_specified|ACTN1-related_disorder|not_provided": 1,
    "Macrothrombocytopenia|Platelet-type_bleeding_disorder_15|not_provided": 1,
    "not_provided|Platelet-type_bleeding_disorder_15|ACTN1-related_disorder|Macrothrombocytopenia|Inborn_genetic_diseases|Thrombocytopenia": 1,
    "SLC10A1-related_disorder": 31,
    "SLC10A1-related_disorder|not_provided": 10,
    "SLC10A1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Hypercholanemia|_familial|_2": 2,
    "Hepatitis_B_virus|_resistance_to|Hypercholanemia|_familial|_2|not_provided|not_specified": 1,
    "Hypercholanemia|_familial|_2|not_provided|SLC10A1-related_disorder": 1,
    "Hypercholanemia|_familial|_2": 3,
    "Hypercholanemia|_familial|_2|SLC10A1-related_disorder": 1,
    "not_provided|SLC10A1-related_disorder": 3,
    "not_specified|SLC10A1-related_disorder": 1,
    "not_provided|not_specified|SLC10A1-related_disorder": 1,
    "not_specified|Hypercholanemia|_familial|_2|not_provided": 1,
    "SLC10A1-related_disorder|not_specified|Hypercholanemia|_familial|_2": 1,
    "SLC10A1-related_disorder|Hypercholanemia|_familial|_2|not_provided": 1,
    "not_provided|Hypercholanemia|_familial|_2": 1,
    "SLC10A1-related_disorder|Hypercholanemia|_familial|_2": 1,
    "Hypercholanemia|_familial|_2|not_provided": 1,
    "SMOC1-related_disorder|not_provided": 3,
    "not_provided|Microphthalmia_with_limb_anomalies|not_specified": 2,
    "not_provided|SMOC1-related_disorder": 3,
    "Microphthalmia_with_limb_anomalies|not_provided": 1,
    "Microphthalmia_with_limb_anomalies": 13,
    "not_specified|not_provided|Microphthalmia_with_limb_anomalies": 1,
    "SMOC1-related_disorder": 2,
    "not_provided|Microphthalmia_with_limb_anomalies": 3,
    "not_provided|not_specified|Microphthalmia_with_limb_anomalies": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_22": 2,
    "Telomere_length|_mean_leukocyte": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3|PSEN1-related_disorder|not_provided": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease": 14,
    "Dilated_Cardiomyopathy|_Dominant|Early-onset_autosomal_dominant_Alzheimer_disease|not_provided|Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia": 1,
    "Alzheimer_disease_3|Dilated_cardiomyopathy_1U": 32,
    "Dilated_cardiomyopathy_1U|Alzheimer_disease_3": 56,
    "not_provided|Alzheimer_disease_3|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease": 1,
    "Dilated_cardiomyopathy_1U|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3": 4,
    "Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia|Alzheimer_disease_3": 8,
    "not_specified|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|Dilated_cardiomyopathy_1U": 1,
    "Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3": 18,
    "Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia": 7,
    "not_specified|Alzheimer_disease_3|Acne_inversa|_familial|_3|Pick_disease|Frontotemporal_dementia": 3,
    "not_specified|not_provided|Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease": 1,
    "not_specified|not_provided|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease": 1,
    "PSEN1-related_disorder|Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Alzheimer_disease_3|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease": 2,
    "Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|Dilated_cardiomyopathy_1U": 1,
    "Pick_disease|Acne_inversa|_familial|_3|Alzheimer_disease_3|Frontotemporal_dementia": 6,
    "Inborn_genetic_diseases|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|not_specified": 1,
    "Acne_inversa|_familial|_3|Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Inborn_genetic_diseases": 2,
    "Acne_inversa|_familial|_3|Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease": 2,
    "not_specified|Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3": 15,
    "Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia": 12,
    "PSEN1-related_disorder": 9,
    "Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3|Alzheimer_disease_3": 14,
    "Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|not_provided|Inborn_genetic_diseases|not_specified|Dilated_cardiomyopathy_1U": 1,
    "Dementia|Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3|not_provided": 1,
    "Pick_disease|Alzheimer_disease_3|Frontotemporal_dementia|not_provided|Alzheimer_disease|_familial|_3|_with_spastic_paraparesis_and_apraxia": 1,
    "Alzheimer_disease_3": 19,
    "Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3": 5,
    "not_provided|Alzheimer_disease_3": 14,
    "Alzheimer_disease_3|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease": 6,
    "not_provided|Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease": 3,
    "PSEN1-related_disorder|Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|not_provided": 1,
    "Alzheimer_disease_3|Acne_inversa|_familial|_3|Pick_disease|Frontotemporal_dementia": 2,
    "Mental_deterioration|Dementia": 1,
    "not_specified|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease": 1,
    "not_provided|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3": 1,
    "Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia|Inborn_genetic_diseases": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|not_provided": 20,
    "Frontotemporal_dementia|Alzheimer_disease_3": 1,
    "Alzheimer_disease_3|not_provided": 5,
    "Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_3": 2,
    "Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|Dilated_cardiomyopathy_1U": 1,
    "Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|Frontotemporal_dementia": 3,
    "Pick_disease|Acne_inversa|_familial|_3|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|Frontotemporal_dementia|Alzheimer_disease": 1,
    "Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease|not_provided": 2,
    "not_provided|Pick_disease": 4,
    "Frontotemporal_dementia|Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3": 2,
    "Alzheimer_disease|_familial|_3|_with_spastic_paraparesis_and_unusual_plaques|not_provided": 2,
    "Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_3|Frontotemporal_dementia|PSEN1-related_disorder": 1,
    "Frontotemporal_dementia|Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3|not_provided": 2,
    "not_provided|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|not_specified": 1,
    "Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|not_provided|Dilated_cardiomyopathy_1U|PSEN1-related_disorder": 1,
    "Pick_disease|Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia": 1,
    "not_provided|PSEN1-related_disorder": 2,
    "Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|not_specified": 1,
    "Pick_disease|Alzheimer_disease_3|not_provided": 1,
    "PSEN1-related_disorder|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease|Dilated_cardiomyopathy_1U|not_provided": 1,
    "Alzheimer_disease_3|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease|not_provided": 1,
    "Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_3|Frontotemporal_dementia|Alzheimer_disease|_familial|_3|_with_unusual_plaques": 1,
    "not_provided|Familial_Alzheimer_disease": 1,
    "PSEN1-related_disorder|Alzheimer_disease_3|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease": 1,
    "Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_3|Frontotemporal_dementia": 2,
    "Pick_disease|Frontotemporal_dementia|Alzheimer_disease_3|Acne_inversa|_familial|_3": 2,
    "not_provided|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease": 1,
    "Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|not_provided": 1,
    "Visual_hallucination|Dementia|Auditory_hallucination|not_provided": 1,
    "Acne_inversa|_familial|_3": 1,
    "Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|not_provided": 4,
    "PSEN1-related_disorder|not_specified|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_3|not_provided": 1,
    "Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease": 2,
    "PSEN1-related_disorder|Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia": 2,
    "Alzheimer_disease_3|Acne_inversa|_familial|_3|Pick_disease|Frontotemporal_dementia|not_provided": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Early_onset_Alzheimer_disease_with_behavioral_disturbance": 1,
    "Alzheimer_disease_3|not_provided|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease": 1,
    "Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3|Pick_disease|not_provided|Mental_deterioration|Dementia": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3|PSEN1-related_disorder|Dilated_cardiomyopathy_1U": 1,
    "Alzheimer_disease|_familial|_3|_with_spastic_paraparesis_and_apraxia|Alzheimer_disease_3": 1,
    "PSEN1-related_disorder|Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3": 1,
    "not_specified|Alzheimer_disease_3|not_provided": 1,
    "Alzheimer_disease_4|not_provided|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_3": 1,
    "Alzheimer_disease|_familial|_3|_with_unusual_plaques|Spastic_paraparesis|Alzheimer_disease_3|not_provided|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3": 1,
    "Alzheimer_disease|_familial|_with_spastic_paraparesis_and_unusual_plaques|Abnormality_of_the_nervous_system": 1,
    "Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|Alzheimer_disease_3": 2,
    "not_provided|Alzheimer_disease|_familial|_with_spastic_paraparesis_and_unusual_plaques|Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease": 1,
    "Pick_disease|Acne_inversa|_familial|_3|Alzheimer_disease_3|Frontotemporal_dementia|Inborn_genetic_diseases": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Early-onset_autosomal_dominant_Alzheimer_disease|not_provided": 1,
    "Early-onset_autosomal_dominant_Alzheimer_disease|not_provided|Alzheimer_disease_3": 1,
    "Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease|not_specified|not_provided|Alzheimer_disease_3|Dilated_cardiomyopathy_1U": 1,
    "Alzheimer_disease_3|Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia|Alzheimer_disease": 1,
    "not_provided|Alzheimer_disease_3|Alzheimer_disease|_familial|_with_spastic_paraparesis_and_unusual_plaques": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3|PSEN1-related_disorder": 1,
    "not_specified|Alzheimer_disease_3|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|PSEN1-related_disorder": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|not_specified|not_provided|Dilated_cardiomyopathy_1U|Alzheimer_disease": 1,
    "Dilated_cardiomyopathy_1U|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|Primary_dilated_cardiomyopathy|Heart_failure": 1,
    "not_provided|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|PSEN1-related_disorder|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3": 1,
    "not_provided|not_specified|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease": 1,
    "Acne_inversa|_familial|_3|Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|not_specified": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|not_specified|not_provided": 1,
    "Alzheimer_disease_3|Dilated_cardiomyopathy_1U|Frontotemporal_dementia|Pick_disease|Acne_inversa|_familial|_3": 1,
    "Alzheimer_disease_3|Frontotemporal_dementia|Acne_inversa|_familial|_3|Pick_disease|Alzheimer_disease_familial_3|_with_spastic_paraparesis": 1,
    "not_provided|not_specified|PSEN1-related_disorder": 1,
    "Alzheimer_disease_3|Dilated_cardiomyopathy_1U|Pick_disease|Frontotemporal_dementia|Acne_inversa|_familial|_3|not_provided": 1,
    "not_provided|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Acne_inversa|_familial|_3|Dilated_cardiomyopathy_1U": 1,
    "not_specified|Acne_inversa|_familial|_3|Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease": 1,
    "Acne_inversa|_familial|_3|Pick_disease|Frontotemporal_dementia|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|not_provided": 1,
    "Frontotemporal_dementia|Alzheimer_disease_3|Acne_inversa|_familial|_3|Pick_disease|not_provided": 1,
    "Pick_disease|Acne_inversa|_familial|_3|Frontotemporal_dementia|Alzheimer_disease_3|not_specified": 1,
    "not_provided|Pick_disease|Frontotemporal_dementia|Alzheimer_disease_3|Acne_inversa|_familial|_3": 1,
    "PSEN1-related_disorder|not_provided|Acne_inversa|_familial|_3|Frontotemporal_dementia|Pick_disease|Alzheimer_disease_3|Dilated_cardiomyopathy_1U|not_specified": 1,
    "Alzheimer_disease_3|Dilated_cardiomyopathy_1U|not_provided": 5,
    "Dilated_cardiomyopathy_1U|not_provided|Alzheimer_disease_3": 4,
    "Alzheimer_disease_3|Frontotemporal_dementia|Pick_disease|Dilated_cardiomyopathy_1U|Acne_inversa|_familial|_3": 1,
    "Dilated_cardiomyopathy_1U|Alzheimer_disease_3|not_provided": 2,
    "Alzheimer_disease_3|not_provided|Dilated_cardiomyopathy_1U": 1,
    "Early-onset_autosomal_dominant_Alzheimer_disease|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|Early-onset_autosomal_dominant_Alzheimer_disease|not_provided": 1,
    "not_provided|Alzheimer_disease_3|Dilated_cardiomyopathy_1U": 2,
    "not_provided|Dilated_cardiomyopathy_1U|Alzheimer_disease_3": 2,
    "Primary_ciliary_dyskinesia_16": 61,
    "not_provided|Primary_ciliary_dyskinesia_16": 1,
    "DNAL1-related_disorder": 1,
    "DNAL1-related_disorder|Primary_ciliary_dyskinesia_16": 1,
    "Primary_ciliary_dyskinesia_16|DNAL1-related_disorder": 1,
    "Primary_ciliary_dyskinesia_16|not_specified": 3,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_16": 2,
    "Inborn_genetic_diseases|not_specified|Primary_ciliary_dyskinesia_16": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_16": 1,
    "Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia_16": 2,
    "not_provided|Primary_ciliary_dyskinesia_16|not_specified": 1,
    "Primary_ciliary_dyskinesia_16|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia_16|Inborn_genetic_diseases": 1,
    "not_specified|Primary_ciliary_dyskinesia_16|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia_16|not_specified|not_provided": 1,
    "COQ6-related_disorder|not_specified|not_provided|Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness": 1,
    "not_provided|COQ6-related_disorder": 6,
    "Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness": 58,
    "Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness|Inborn_genetic_diseases|not_provided": 2,
    "Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness|not_provided": 14,
    "not_provided|Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness": 14,
    "COQ6-related_disorder|not_provided": 4,
    "Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness": 2,
    "not_provided|Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness|COQ6-related_disorder": 2,
    "not_specified|not_provided|Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness": 4,
    "Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness|not_provided|Inborn_genetic_diseases": 3,
    "COQ6-related_disorder": 2,
    "not_provided|Familial_steroid-resistant_nephrotic_syndrome_with_sensorineural_deafness|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|increased_susceptibility_to_pneumonia": 1,
    "not_provided|Methylmalonate_semialdehyde_dehydrogenase_deficiency": 22,
    "Methylmalonate_semialdehyde_dehydrogenase_deficiency": 59,
    "Methylmalonate_semialdehyde_dehydrogenase_deficiency|not_provided": 19,
    "Methylmalonate_semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases": 2,
    "ALDH6A1-related_disorder|not_provided": 3,
    "Methylmalonate_semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "ALDH6A1-related_disorder": 2,
    "Methylmalonate_semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Methylmalonate_semialdehyde_dehydrogenase_deficiency": 1,
    "Methylmalonate_semialdehyde_dehydrogenase_deficiency|ALDH6A1-related_disorder|not_provided": 1,
    "ALDH6A1-related_disorder|Methylmalonate_semialdehyde_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3": 29,
    "VSX2-related_Microphthalmia|Isolated_microphthalmia_6|not_provided": 1,
    "Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2": 26,
    "Isolated_microphthalmia_2": 254,
    "Anophthalmia-microphthalmia_syndrome|Isolated_microphthalmia_2": 1,
    "Isolated_microphthalmia_2|VSX2-related_disorder": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_2": 3,
    "Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3|not_provided|VSX2-related_disorder|Microphthalmia": 1,
    "Microphthalmia|Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3": 1,
    "Isolated_microphthalmia_2|Microphthalmia": 8,
    "Microphthalmia|Isolated_microphthalmia_2": 7,
    "not_provided|Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3": 1,
    "Microphthalmia|Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3|VSX2-related_disorder": 2,
    "Microphthalmia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Microphthalmia|Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3": 1,
    "Isolated_microphthalmia_2|Inborn_genetic_diseases": 1,
    "Microphthalmia|_isolated|_with_coloboma_3": 2,
    "not_provided|Isolated_microphthalmia_2|Microphthalmia": 1,
    "VSX2-related_disorder": 2,
    "Microphthalmia|Isolated_microphthalmia_2|not_provided|Microphthalmia|_isolated|_with_coloboma_3|not_specified": 1,
    "VSX2-related_disorder|not_provided": 2,
    "Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3|not_provided": 9,
    "VSX2-related_disorder|not_specified|not_provided|Microphthalmia|Isolated_microphthalmia_2": 1,
    "Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2|Inborn_genetic_diseases": 1,
    "Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2|Microphthalmia": 4,
    "Microphthalmia|_cataracts|_and_iris_abnormalities|Isolated_microphthalmia_2": 1,
    "VSX2-related_disorder|not_provided|Microphthalmia|_cataracts|_and_iris_abnormalities|Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3": 1,
    "Isolated_microphthalmia_2|VSX2-related_disorder|Microphthalmia": 1,
    "Anophthalmia-microphthalmia_syndrome|Microphthalmia|Isolated_microphthalmia_2|VSX2-related_Microphthalmia": 1,
    "VSX2-related_Microphthalmia|Anophthalmia|Microphthalmia|Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2": 1,
    "Isolated_microphthalmia_2|Microphthalmia|_isolated|_with_coloboma_3|VSX2-related_disorder": 1,
    "Isolated_microphthalmia_2|not_provided|Microphthalmia": 2,
    "not_provided|Isolated_microphthalmia_2": 1,
    "not_provided|Inborn_genetic_diseases|Isolated_microphthalmia_2": 1,
    "Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2|Microphthalmia|not_provided|not_specified": 1,
    "Isolated_microphthalmia_2|Microphthalmia|Microphthalmia|_isolated|_with_coloboma_3": 1,
    "VSX2-related_Microphthalmia|Isolated_microphthalmia_6|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Microphthalmia|_isolated|_with_coloboma_3": 1,
    "not_provided|Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2|not_specified": 1,
    "VSX2-related_disorder|Isolated_microphthalmia_2": 1,
    "VSX2-related_disorder|Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2": 1,
    "Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2|not_provided": 5,
    "not_provided|Microphthalmia|_isolated|_with_coloboma_3|Isolated_microphthalmia_2": 2,
    "VSX2-related_Microphthalmia|Isolated_microphthalmia_6": 2,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 212,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_specified": 6,
    "not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 5,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 14,
    "ABCD4-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_specified|not_provided": 1,
    "not_provided|not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 6,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_specified": 7,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|Inborn_genetic_diseases": 7,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|Inborn_genetic_diseases": 3,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided": 1,
    "not_provided|Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided": 7,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided": 5,
    "ABCD4-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "ABCD4-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided|ABCD4-related_disorder": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 12,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided|Inborn_genetic_diseases": 1,
    "Cobalamin_C_disease|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|ABCD4-related_disorder": 1,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|ABCD4-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided|ABCD4-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_specified": 2,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|Cobalamin_C_disease": 1,
    "not_provided|ABCD4-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|ABCD4-related_disorder|not_specified": 2,
    "not_specified|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 3,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblJ|not_provided|Cobalamin_C_disease": 1,
    "not_specified|Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblJ": 1,
    "not_provided|Niemann-Pick_disease|_type_C1": 70,
    "Niemann-Pick_disease|_type_C1": 1864,
    "Niemann-Pick_disease|_type_C1|not_provided|not_specified": 2,
    "Niemann-Pick_disease|_type_C2": 207,
    "Niemann-Pick_disease|_type_C2|not_provided": 4,
    "NPC2-related_disorder|Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C2": 1,
    "Niemann-Pick_disease|_type_C2|not_provided|Niemann-Pick_disease|_type_C1|not_specified": 1,
    "NPC2-related_disorder": 5,
    "NPC2-related_disorder|not_specified|not_provided|Niemann-Pick_disease|_type_C2|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C2": 3,
    "not_provided|Niemann-Pick_disease|_type_C2": 3,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C2": 5,
    "Niemann-Pick_disease|_type_C2|Niemann-Pick_disease|_type_C1|not_specified|not_provided": 1,
    "Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C2|Niemann-Pick_disease|_type_C": 1,
    "Niemann-Pick_disease|_type_C2|Niemann-Pick_disease|_type_C": 3,
    "Niemann-Pick_disease|_type_C2|Inborn_genetic_diseases": 3,
    "Niemann-Pick_disease|_type_C2|Inborn_genetic_diseases|not_specified|NPC2-related_disorder|not_provided": 1,
    "Niemann-Pick_disease|_type_C2|not_specified": 1,
    "Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C2": 1,
    "Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C2": 3,
    "not_provided|Niemann-Pick_disease|_type_C2|NPC2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C2|NPC2-related_disorder|Inborn_genetic_diseases": 1,
    "Niemann-Pick_disease|_type_C2|NPC2-related_disorder": 2,
    "not_provided|not_specified|Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C2": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C2|not_provided": 1,
    "NPC2-related_disorder|not_provided|Niemann-Pick_disease|_type_C2": 1,
    "not_specified|not_provided|Niemann-Pick_disease|_type_C2|Microcephaly|Brain_atrophy|Seizure|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C2|Niemann-Pick_disease|_type_C": 1,
    "Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C2": 1,
    "NPC2-related_disorder|Niemann-Pick_disease|_type_C2": 2,
    "Niemann-Pick_disease|_type_C": 13,
    "Multiple_mitochondrial_dysfunctions_syndrome_4": 4,
    "ISCA2-related_disorder": 1,
    "ISCA2-related_disorder|not_provided": 2,
    "Multiple_mitochondrial_dysfunctions_syndrome_4|not_provided": 1,
    "Fatal_multiple_mitochondrial_dysfunctions_syndrome|Multiple_mitochondrial_dysfunctions_syndrome_4|not_provided|Optic_atrophy|Spastic_quadriplegic_cerebral_palsy|Failure_to_thrive|Axial_hypotonia|High_CSF_lactic_acid|Neurodegeration|Global_developmental_delay|Death_in_infancy": 1,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_4": 2,
    "not_provided|ISCA2-related_disorder": 1,
    "not_specified|Multiple_mitochondrial_dysfunctions_syndrome_4": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_4|Inborn_genetic_diseases|not_provided": 2,
    "Weill-Marchesani_syndrome|not_provided|Glaucoma_3|_primary_congenital|_D": 17,
    "Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D": 31,
    "Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D|not_provided": 15,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome": 33,
    "Glaucoma_3|_primary_congenital|_D|not_provided|Weill-Marchesani_syndrome": 6,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided": 23,
    "Primary_congenital_glaucoma|Weill-Marchesani_syndrome": 2,
    "Primary_congenital_glaucoma|Weill-Marchesani_syndrome|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D": 1,
    "Microspherophakia": 5,
    "Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided|Inborn_genetic_diseases": 1,
    "Weill-Marchesani_syndrome|Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D|not_provided": 1,
    "Glaucoma_3A|Glaucoma_3|_primary_congenital|_D": 2,
    "LTBP2-related_disorder|Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D|not_provided|Inborn_genetic_diseases": 1,
    "LTBP2-related_disorder": 3,
    "LTBP2-related_disorder|not_provided": 13,
    "not_provided|Weill-Marchesani_syndrome|not_specified|Glaucoma_3|_primary_congenital|_D": 1,
    "not_provided|Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D": 4,
    "not_provided|not_specified|Glaucoma_3|_primary_congenital|_D": 1,
    "Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D|Microspherophakia|not_provided|Glaucoma_3|_primary_infantile|_B": 1,
    "not_provided|Primary_open_angle_glaucoma|Glaucoma_3|_primary_congenital|_D|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma": 1,
    "Glaucoma_3|_primary_congenital|_D|LTBP2-related_disorder|Weill-Marchesani_syndrome|not_provided": 2,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_infantile|_B|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma": 2,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_congenital|_D|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|not_specified|Weill-Marchesani_syndrome": 3,
    "not_provided|Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3": 2,
    "Weill-Marchesani_syndrome|not_provided|not_specified|Glaucoma_3|_primary_congenital|_D": 1,
    "Pseudoexfoliation_glaucoma|Glaucoma_3|_primary_congenital|_D|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided": 1,
    "Primary_open_angle_glaucoma|not_provided": 2,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|LTBP2-related_disorder": 2,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Glaucoma_3|_primary_infantile|_B|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3": 1,
    "Glaucoma_3|_primary_congenital|_D|Inborn_genetic_diseases|Weill-Marchesani_syndrome": 2,
    "Weill-Marchesani_syndrome_3|LTBP2-related_disorder|Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided": 1,
    "not_provided|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B": 1,
    "Glaucoma_3|_primary_congenital|_D|Microspherophakia|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome": 14,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Glaucoma_3|_primary_infantile|_B|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Inborn_genetic_diseases|Weill-Marchesani_syndrome": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_D|not_provided|Primary_open_angle_glaucoma": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|not_provided": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|LTBP2-related_disorder|Weill-Marchesani_syndrome": 2,
    "Weill-Marchesani_syndrome|not_provided|Glaucoma_3|_primary_congenital|_D|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|LTBP2-related_disorder": 2,
    "not_provided|LTBP2-related_disorder|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma": 3,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3": 1,
    "not_provided|LTBP2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Weill-Marchesani_syndrome|not_provided|Glaucoma_3|_primary_congenital|_D": 3,
    "Glaucoma_3|_primary_infantile|_B|not_provided": 1,
    "Weill-Marchesani_syndrome|Primary_congenital_glaucoma|not_provided": 1,
    "Weill-Marchesani_syndrome|not_provided|Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D": 1,
    "not_provided|LTBP2-related_disorder": 4,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D|Microspherophakia|Weill-Marchesani_syndrome|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|Primary_open_angle_glaucoma|not_provided": 1,
    "Weill-Marchesani_syndrome_3|Weill-Marchesani_syndrome_1": 1,
    "LTBP2-related_disorder|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided": 1,
    "Pseudoexfoliation_glaucoma|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided": 1,
    "Weill-Marchesani_syndrome_3|Inborn_genetic_diseases|Microspherophakia|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D": 2,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome": 1,
    "Weill-Marchesani_syndrome|not_specified|not_provided|Glaucoma_3|_primary_congenital|_D": 1,
    "Glaucoma_3|_primary_congenital|_D|Alveolar_capillary_dysplasia_without_misalignment_of_pulmonary_veins|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Inborn_genetic_diseases|not_provided|Weill-Marchesani_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|LTBP2-related_disorder": 1,
    "Weill-Marchesani_syndrome|not_provided|Glaucoma_3|_primary_congenital|_D|not_specified": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3": 1,
    "Inborn_genetic_diseases|not_provided|Glaucoma_3|_primary_infantile|_B|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D": 1,
    "LTBP2-related_disorder|not_provided|Glaucoma_3|_primary_congenital|_D": 1,
    "Glaucoma_3|_primary_congenital|_D|not_provided|LTBP2-related_disorder|Weill-Marchesani_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D": 1,
    "Weill-Marchesani_syndrome_3|not_specified|not_provided|Microspherophakia": 1,
    "Weill-Marchesani_syndrome_3": 2,
    "not_provided|Weill-Marchesani_syndrome_3": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Microspherophakia|not_specified|Weill-Marchesani_syndrome_3|Weill-Marchesani_syndrome": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D|not_provided|Weill-Marchesani_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Microspherophakia": 1,
    "Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia|not_provided|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma": 1,
    "Pseudoexfoliation_glaucoma|not_provided": 1,
    "not_provided|Microspherophakia|Weill-Marchesani_syndrome_3": 2,
    "Weill-Marchesani_syndrome|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided|Glaucoma_3|_primary_infantile|_B": 1,
    "Weill-Marchesani_syndrome|LTBP2-related_disorder|Glaucoma_3|_primary_congenital|_D|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|not_provided|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_infantile|_B|LTBP2-related_disorder|Weill-Marchesani_syndrome": 1,
    "Weill-Marchesani_syndrome|not_specified|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Glaucoma_3|_primary_congenital|_D": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Inborn_genetic_diseases|LTBP2-related_disorder|Weill-Marchesani_syndrome": 1,
    "Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|not_provided|Inborn_genetic_diseases": 1,
    "Glaucoma_3|_primary_congenital|_D": 5,
    "Glaucoma_3|_primary_congenital|_D|not_provided|LTBP2-related_disorder|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome_3|Weill-Marchesani_syndrome": 1,
    "Glaucoma_3|_primary_congenital|_D|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Weill-Marchesani_syndrome|not_provided|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Inborn_genetic_diseases": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|LTBP2-related_disorder|Weill-Marchesani_syndrome|not_provided|Pseudoexfoliation_glaucoma": 1,
    "Weill-Marchesani_syndrome|Inborn_genetic_diseases|Glaucoma_3|_primary_congenital|_D": 1,
    "Glaucoma_3|_primary_congenital|_D|not_provided|not_specified|Weill-Marchesani_syndrome": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Inborn_genetic_diseases|not_provided": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided|Microspherophakia|Glaucoma_3|_primary_congenital|_D": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_congenital|_D|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Microspherophakia|not_provided|LTBP2-related_disorder": 1,
    "Weill-Marchesani_syndrome_3|not_provided|LTBP2-related_disorder": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_provided|Weill-Marchesani_syndrome_3": 1,
    "not_provided|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_infantile|_B|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_congenital|_D": 1,
    "Glaucoma_3|_primary_infantile|_B|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|not_provided": 1,
    "Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|LTBP2-related_disorder|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|LTBP2-related_disorder|Inborn_genetic_diseases|Weill-Marchesani_syndrome|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome_3|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Inborn_genetic_diseases|Weill-Marchesani_syndrome|not_provided": 1,
    "Glaucoma_3|_primary_congenital|_D|not_provided|Weill-Marchesani_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|not_specified": 1,
    "Glaucoma_3|_primary_congenital|_D|Weill-Marchesani_syndrome|Microspherophakia_and/or_megalocornea|_with_ectopia_lentis_and_with_or_without_secondary_glaucoma|Glaucoma_3|_primary_infantile|_B|Weill-Marchesani_syndrome_3": 1,
    "DLST-related_disorder": 5,
    "not_provided|DLST-related_disorder": 6,
    "DLST-related_disorder|not_provided": 4,
    "not_provided|DLST-related_disorder|not_specified": 1,
    "not_specified|DLST-related_disorder": 1,
    "not_provided|Pheochromocytoma/paraganglioma_syndrome_7|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_7|Hereditary_pheochromocytoma-paraganglioma": 1,
    "Pheochromocytoma/paraganglioma_syndrome_7": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_2|not_provided": 4,
    "Leukoencephalopathy_with_vanishing_white_matter_2|not_provided|Vanishing_white_matter_disease|Abnormality_of_the_nervous_system": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_2|not_provided": 3,
    "EIF2B2-related_disorder|not_provided|Vanishing_white_matter_disease": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_2": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_2": 4,
    "Leukoencephalopathy_with_vanishing_white_matter_2|Inborn_genetic_diseases|not_provided|Vanishing_white_matter_disease|See_cases|EIF2B2-related_disorder": 1,
    "EIF2B2-related_disorder": 2,
    "EIF2B2-related_disorder|Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_1|not_provided|Leukoencephalopathy_with_vanishing_white_matter_2|See_cases": 1,
    "Vanishing_white_matter_disease|Leukoencephalopathy_with_vanishing_white_matter_2|not_provided|Osteogenesis_imperfecta|Premature_ovarian_insufficiency": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|EIF2B2-related_disorder|Leukoencephalopathy_with_vanishing_white_matter_2|Vanishing_white_matter_disease|Abnormality_of_the_nervous_system": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_2|not_provided|Vanishing_white_matter_disease": 1,
    "Lynch_syndrome|Vanishing_white_matter_disease|not_specified|not_provided": 1,
    "Lynch_syndrome|Vanishing_white_matter_disease": 1,
    "Lynch_syndrome|not_provided|Vanishing_white_matter_disease": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 361,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided|Vanishing_white_matter_disease": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Vanishing_white_matter_disease": 1,
    "Lynch_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Vanishing_white_matter_disease|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided": 7,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 2,
    "MLH3-related_disorder": 7,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 311,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 339,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_specified|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|not_specified|not_provided": 5,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|MLH3-related_disorder|not_provided|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer": 5,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|Colorectal_cancer|Endometrial_carcinoma": 3,
    "Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|not_specified": 2,
    "Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma": 8,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder": 8,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|MLH3-related_disorder": 1,
    "Colorectal_cancer|_non-polyposis|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|MLH3-related_disorder": 5,
    "not_specified|MLH3-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_specified": 16,
    "not_specified|MLH3-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 6,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|Endometrial_carcinoma|Colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma": 9,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided": 2,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma": 2,
    "not_specified|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer": 11,
    "not_specified|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma": 3,
    "not_specified|MLH3-related_disorder": 5,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma|MLH3-related_disorder": 1,
    "not_specified|Colorectal_cancer|MLH3-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|MLH3-related_disorder": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|Endometrial_carcinoma|Colorectal_cancer": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|not_specified": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_provided": 1,
    "Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|not_specified": 3,
    "MLH3-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 4,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Ovarian_cancer": 2,
    "Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|MLH3-related_disorder": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided|Colorectal_cancer": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|MLH3-related_disorder|not_specified": 1,
    "Endometrial_carcinoma|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 5,
    "Hereditary_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|not_specified|not_provided|Colorectal_cancer|Endometrial_carcinoma|Lynch_syndrome": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|MLH3-related_disorder|Ovarian_cancer|not_specified": 1,
    "not_specified|Endometrial_carcinoma|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 5,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer": 8,
    "MLH3-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 6,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma|MLH3-related_disorder|not_specified": 2,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_specified": 1,
    "MLH3-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 4,
    "MLH3-related_disorder|not_specified": 9,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided|Endometrial_carcinoma|Colorectal_cancer": 1,
    "not_specified|Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 7,
    "Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 7,
    "Colorectal_cancer|_non-polyposis|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|not_specified|not_provided|Endometrial_carcinoma|Colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided|Endometrial_carcinoma|MLH3-related_disorder|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided|Endometrial_carcinoma|not_specified": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|not_specified|not_provided|Colorectal_cancer": 2,
    "Ovarian_cancer|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 2,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Lynch_syndrome_1": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma|not_specified": 10,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|not_specified": 6,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|Endometrial_carcinoma": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|not_specified": 6,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|not_specified|not_provided": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_specified|MLH3-related_disorder": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided|Endometrial_carcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|not_provided": 1,
    "Endometrial_carcinoma|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder|not_specified|not_provided": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_non-polyposis|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|MLH3-related_disorder|not_provided": 1,
    "Endometrial_carcinoma|not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Lynch_syndrome_1|Malignant_tumor_of_breast": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided": 1,
    "not_provided|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma|not_specified|not_provided": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|MLH3-related_disorder|Endometrial_carcinoma|Colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided|Colorectal_cancer|Endometrial_carcinoma": 1,
    "Ovarian_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|MLH3-related_disorder|not_specified": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Ovarian_cancer|not_specified": 1,
    "Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Lynch_syndrome_1|not_specified": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|Endometrial_carcinoma|not_provided|Colorectal_cancer": 2,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided|not_specified": 1,
    "not_provided|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_specified": 1,
    "not_specified|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma": 1,
    "MLH3-related_disorder|Endometrial_carcinoma|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified": 1,
    "Endometrial_carcinoma|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided|MLH3-related_disorder|not_specified": 1,
    "Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer": 1,
    "Astrocytoma_IDH-mutant|not_specified": 1,
    "Premature_ovarian_failure|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "not_provided|MLH3-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "MLH3-related_disorder|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|Endometrial_carcinoma|not_specified": 1,
    "not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|MLH3-related_disorder|not_specified": 1,
    "not_specified|not_provided|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|MLH3-related_disorder": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|MLH3-related_disorder": 1,
    "MLH3-related_disorder|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer|not_specified": 1,
    "MLH3-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|not_provided": 1,
    "not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_provided": 2,
    "not_specified|not_provided|Endometrial_carcinoma|Colorectal_cancer|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|Endometrial_cancer": 1,
    "Colorectal_cancer|MLH3-related_disorder|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|MLH3-related_disorder|not_provided": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided|Colorectal_cancer": 2,
    "Endometrial_carcinoma|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided|MLH3-related_disorder|Colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|MLH3-related_disorder|not_provided|Endometrial_carcinoma|Colorectal_cancer": 1,
    "Colorectal_cancer|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|not_specified|not_provided": 1,
    "Ovarian_cancer|not_specified|Endometrial_carcinoma|Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Colorectal_cancer": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Colorectal_cancer|MLH3-related_disorder|not_specified|not_provided": 1,
    "Colorectal_cancer|_hereditary_nonpolyposis|_type_7|Endometrial_carcinoma|Hereditary_cancer|not_specified|Colorectal_cancer|not_provided": 1,
    "Hereditary_nonpolyposis_colorectal_neoplasms|not_specified|Colorectal_cancer|_hereditary_nonpolyposis|_type_7": 1,
    "NEK9-related_lethal_skeletal_dysplasia|Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy|not_provided": 2,
    "Inborn_genetic_diseases|NEK9-related_disorder": 2,
    "NEK9-related_lethal_skeletal_dysplasia": 5,
    "not_provided|NEK9-related_disorder": 3,
    "NEK9-related_disorder|not_provided": 3,
    "Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy|not_provided": 2,
    "NEK9-related_lethal_skeletal_dysplasia|Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy": 1,
    "NEK9-related_disorder|Inborn_genetic_diseases": 1,
    "NEK9-related_lethal_skeletal_dysplasia|not_provided|NEK9-related_disorder": 1,
    "Inborn_genetic_diseases|Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy": 1,
    "Nevus_comedonicus_syndrome": 2,
    "Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy|NEK9-related_lethal_skeletal_dysplasia": 2,
    "Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy": 4,
    "NEK9-related_disorder": 3,
    "Congenital_omphalocele|Congenital_contracture": 1,
    "Arthrogryposis|_Perthes_disease|_and_upward_gaze_palsy|NEK9-related_lethal_skeletal_dysplasia|not_provided": 1,
    "Fowler_syndrome|not_provided": 1,
    "not_provided|Fowler_syndrome": 2,
    "not_specified|not_provided|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|Fowler_syndrome": 1,
    "not_provided|FLVCR2-related_disorder": 5,
    "Fowler_syndrome": 20,
    "not_specified|not_provided|Fowler_syndrome|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "not_provided|Fowler_syndrome|not_specified|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "not_provided|FLVCR2-related_disorder|Posterior_column_ataxia-retinitis_pigmentosa_syndrome": 1,
    "not_specified|Posterior_column_ataxia-retinitis_pigmentosa_syndrome|FLVCR2-related_disorder|not_provided": 1,
    "Fowler_syndrome|Inborn_genetic_diseases": 1,
    "FLVCR2-related_disorder": 2,
    "FLVCR2-related_disorder|not_provided|Fowler_syndrome": 1,
    "Posterior_column_ataxia-retinitis_pigmentosa_syndrome|FLVCR2-related_disorder|not_provided": 1,
    "TTLL5-related_disorder|not_provided": 7,
    "TTLL5-related_disorder": 1,
    "Cone-rod_dystrophy_19|not_provided": 6,
    "not_provided|Cone-rod_dystrophy_19": 5,
    "not_provided|TTLL5-related_disorder": 10,
    "not_provided|Reduced_sperm_motility|Abnormal_sperm_morphology|Oligospermia": 1,
    "not_provided|Inborn_genetic_diseases|TTLL5-related_disorder": 1,
    "not_provided|Retinal_dystrophy|TTLL5-related_disorder": 1,
    "not_provided|Retinal_dystrophy|Central_areolar_choroidal_dystrophy": 1,
    "Cone-rod_dystrophy_19|Cone-rod_dystrophy": 1,
    "Cone-rod_dystrophy_19|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy_19|not_provided|TTLL5-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Cone-rod_dystrophy_19": 1,
    "Cone-rod_dystrophy_19|Inborn_genetic_diseases": 1,
    "Cone-rod_dystrophy_19": 2,
    "TTLL5-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cone-rod_dystrophy_19": 1,
    "Collapse_(finding)|Premature_ventricular_contraction": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|TGFB3-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 2,
    "Rienhoff_syndrome|not_provided": 20,
    "Rienhoff_syndrome": 229,
    "Rienhoff_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome": 38,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 29,
    "TGFB3-related_disorder": 9,
    "not_provided|not_specified|Rienhoff_syndrome": 1,
    "TGFB3-related_disorder|Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Rienhoff_syndrome": 17,
    "not_provided|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|not_provided": 5,
    "Rienhoff_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 10,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome": 6,
    "Rienhoff_syndrome|TGFB3-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Rienhoff_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Rienhoff_syndrome|not_specified": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_disorder_of_connective_tissue|Rienhoff_syndrome": 1,
    "Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Developmental_disorder|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|not_provided": 1,
    "TGFB3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Rienhoff_syndrome": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome": 3,
    "Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 9,
    "Rienhoff_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Rienhoff_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1": 2,
    "not_provided|Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Rienhoff_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Rienhoff_syndrome": 4,
    "Loeys-Dietz_syndrome|Rienhoff_syndrome": 1,
    "Rienhoff_syndrome|Loeys-Dietz_syndrome": 1,
    "Rienhoff_syndrome|Primary_dilated_cardiomyopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFB3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Rienhoff_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB3-related_disorder|Rienhoff_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Long_QT_syndrome": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|not_specified": 1,
    "not_provided|Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Rienhoff_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Rienhoff_syndrome|TGFB3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Rienhoff_syndrome|Hypertrophic_cardiomyopathy": 1,
    "Brugada_syndrome|Rienhoff_syndrome": 1,
    "Rienhoff_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arrhythmogenic_right_ventricular_dysplasia_1": 2,
    "not_provided|Rienhoff_syndrome|not_specified": 2,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB3-related_disorder|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|not_provided": 1,
    "TGFB3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|not_provided": 1,
    "not_provided|Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Rienhoff_syndrome|not_provided|not_specified": 1,
    "TGFB3-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|not_provided": 1,
    "not_provided|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|TGFB3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome": 1,
    "TGFB3-related_connective_tissue_disorders": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome|not_specified": 1,
    "Rienhoff_syndrome|TGFB3-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "not_specified|Rienhoff_syndrome": 3,
    "TGFB3-related_disorder|Rienhoff_syndrome|not_specified|not_provided|Long_QT_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arrhythmogenic_right_ventricular_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "TGFB3-related_disorder|Rienhoff_syndrome|not_provided|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|not_provided": 1,
    "TGFB3-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB3-related_disorder": 1,
    "Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|TGFB3-related_disorder|not_provided": 1,
    "not_specified|Flexion_contracture": 1,
    "not_specified|Cardiomyopathy|not_provided|Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|TGFB3-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "TGFB3-related_disorder|Rienhoff_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Rienhoff_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Rienhoff_syndrome": 1,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_1|Rienhoff_syndrome|TGFB3-related_disorder|not_provided": 1,
    "not_provided|TGFB3-related_disorder": 1,
    "Rienhoff_syndrome|Arrhythmogenic_right_ventricular_dysplasia_1|Arrhythmogenic_right_ventricular_cardiomyopathy": 3,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cranioectodermal_dysplasia": 2,
    "not_provided|Cranioectodermal_dysplasia_3": 1,
    "Short-rib_thoracic_dysplasia_18_with_polydactyly|Short_rib-polydactyly_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_81|Short-rib_thoracic_dysplasia_18_with_polydactyly|Cranioectodermal_dysplasia_3": 18,
    "Connective_tissue_disorder|not_specified|not_provided|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81": 1,
    "not_provided|IFT43-related_disorder": 2,
    "not_provided|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81": 9,
    "not_specified|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|not_provided": 3,
    "Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3|not_provided": 11,
    "IFT43-related_disorder|not_provided": 1,
    "Short-rib_thoracic_dysplasia_18_with_polydactyly|Jeune_thoracic_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_81": 1,
    "not_provided|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly": 1,
    "Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|not_provided": 7,
    "not_provided|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3": 5,
    "Connective_tissue_disorder|not_provided|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3": 1,
    "Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81": 1,
    "IFT43-related_disorder": 2,
    "not_provided|Retinitis_pigmentosa_81|not_specified": 1,
    "not_provided|Short-rib_thoracic_dysplasia_18_with_polydactyly|Cranioectodermal_dysplasia_3|Retinitis_pigmentosa_81": 1,
    "not_provided|not_specified|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3": 2,
    "Cranioectodermal_dysplasia_3": 1,
    "not_provided|Connective_tissue_disorder|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly": 1,
    "not_provided|Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|not_specified": 2,
    "IFT43-related_disorder|not_provided|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3": 1,
    "Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|not_provided|not_specified": 1,
    "not_specified|not_provided|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3": 1,
    "Cranioectodermal_dysplasia_3|Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|not_specified|not_provided": 1,
    "Short-rib_thoracic_dysplasia_18_with_polydactyly|Retinitis_pigmentosa_81|Cranioectodermal_dysplasia_3|not_specified|not_provided": 1,
    "Short-rib_thoracic_dysplasia_18_with_polydactyly": 1,
    "Short-rib_thoracic_dysplasia_18_with_polydactyly|Short_rib-polydactyly_syndrome": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_35": 53,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_35|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_35|not_provided|not_specified": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_35|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_35|not_provided": 12,
    "ESRRB-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_35": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_35|not_specified": 3,
    "not_specified|Hearing_loss|_autosomal_recessive|Hearing_impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_35|not_specified": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_35": 4,
    "not_provided|ESRRB-related_disorder": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_35": 2,
    "ESRRB-related_disorder|not_specified|not_provided": 1,
    "not_specified|ESRRB-related_disorder": 1,
    "not_provided|ESRRB-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_35": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_35": 2,
    "ESRRB-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_35|not_specified|not_provided": 1,
    "ESRRB-related_disorder": 1,
    "IRF2BPL-related_disorder": 26,
    "Inborn_genetic_diseases|IRF2BPL-related_disorder|Intellectual_disability": 1,
    "not_provided|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures": 7,
    "not_provided|IRF2BPL-related_disorder": 7,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|IRF2BPL-related_disorder": 2,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures": 89,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|not_provided": 10,
    "IRF2BPL-related_disorder|not_provided": 8,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures": 3,
    "IRF2BPL-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|IRF2BPL-related_disorder": 4,
    "Inborn_genetic_diseases|Cleft_palate": 1,
    "not_provided|IRF2BPL-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|not_specified": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|IRF2BPL-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|not_provided|IRF2BPL-related_disorder": 1,
    "IRF2BPL-related_disorder|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures": 1,
    "not_provided|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|IRF2BPL-related_disorder": 1,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|IRF2BPL-related_disorder|not_provided": 1,
    "not_specified|not_provided|IRF2BPL-related_disorder": 1,
    "Developmental_disorder|not_specified|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures": 1,
    "Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|not_specified|not_provided": 1,
    "not_specified|Neurodevelopmental_disorder_with_regression|_abnormal_movements|_loss_of_speech|_and_seizures|not_provided": 1,
    "Spastic_paraplegia_87|_autosomal_recessive": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 73,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 7,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 405,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 44,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2": 29,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 55,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|POMT2-related_disorder": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 37,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 8,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2": 159,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_specified": 6,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified": 14,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified|not_provided": 7,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 29,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2": 22,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|not_specified": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 8,
    "POMT2-related_disorder|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 1,
    "POMT2-related_disorder": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided": 13,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Inborn_genetic_diseases": 7,
    "POMT2-related_disorder|Muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 5,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 3,
    "not_provided|POMT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|Inborn_genetic_diseases": 7,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|not_specified": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 6,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|not_provided": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 8,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 4,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 6,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified": 4,
    "POMT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "POMT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|Inborn_genetic_diseases": 1,
    "Myopathy_caused_by_variation_in_POMT2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Inborn_genetic_diseases": 2,
    "POMT2-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "POMT2-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified": 2,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided|Inborn_genetic_diseases": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Inborn_genetic_diseases|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified|POMT2-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided": 1,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "Myopathy_caused_by_variation_in_POMT2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "POMT2-related_disorder|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "POMT2-related_disorder|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|Intellectual_disability": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_provided|Intellectual_disability": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "POMT2-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "Inborn_genetic_diseases|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|See_cases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2": 1,
    "Congenital_muscular_alpha-dystroglycanopathy_with_brain_and_eye_anomalies": 1,
    "not_provided|Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A2|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B2|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2N": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Congenital_muscular_dystrophy": 1,
    "GSTZ1-related_disorder": 4,
    "Maleylacetoacetate_isomerase_deficiency": 5,
    "GSTZ1-related_disorder|not_provided": 2,
    "not_provided|GSTZ1-related_disorder": 1,
    "Maleylacetoacetate_isomerase_deficiency|not_provided": 1,
    "Maleylacetoacetate_isomerase_deficiency|GSTZ1-related_disorder|not_provided": 1,
    "GSTZ1-related_disorder|not_specified": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2": 51,
    "VIPAS39-related_disorder|not_provided|not_specified": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|not_provided|VIPAS39-related_disorder": 1,
    "not_specified|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|not_provided": 12,
    "not_provided|not_specified|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|Inborn_genetic_diseases": 1,
    "VIPAS39-related_disorder|not_provided": 8,
    "not_provided|VIPAS39-related_disorder": 4,
    "VIPAS39-related_disorder|not_specified|not_provided": 2,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|Inborn_genetic_diseases": 1,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2": 5,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|Inborn_genetic_diseases|VIPAS39-related_disorder": 1,
    "VIPAS39-related_disorder": 7,
    "Inborn_genetic_diseases|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|VIPAS39-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2": 3,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|not_specified|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|not_provided|Arthrogryposis_with_renal_dysfunction_and_cholestasis_syndrome": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|VIPAS39-related_disorder": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|VIPAS39-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|VIPAS39-related_disorder": 1,
    "Inborn_genetic_diseases|VIPAS39-related_disorder": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|Inborn_genetic_diseases": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|not_provided|Inborn_genetic_diseases": 2,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Arthrogryposis|_renal_dysfunction|_and_cholestasis_2|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 424,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_provided": 28,
    "not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 23,
    "not_specified|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 3,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|Inborn_genetic_diseases": 24,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_specified": 2,
    "Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 10,
    "SPTLC2-related_disorder|not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 7,
    "NEUROPATHY|_HEREDITARY_SENSORY_AND_AUTONOMIC|_TYPE_IC|_SEVERE": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 4,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|Inborn_genetic_diseases|not_provided": 6,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|SPTLC2-related_disorder|not_specified|not_provided": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_specified|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_specified": 3,
    "Charcot-Marie-Tooth_disease|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "SPTLC2-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 4,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|SPTLC2-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_specified": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|SPTLC2-related_disorder": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SPTLC2-related_disorder|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "SPTLC2-related_disorder|not_provided|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "not_provided|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|SPTLC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C|Inborn_genetic_diseases": 1,
    "not_provided|SPTLC2-related_disorder|Inborn_genetic_diseases|Neuropathy|_hereditary_sensory_and_autonomic|_type_1C": 1,
    "NRXN3-related_disorder": 34,
    "Short_stature|Relative_macrocephaly": 1,
    "NRXN3-associated_neurodevelopmental_disorder|not_specified": 1,
    "not_specified|not_provided|Short_stature|Relative_macrocephaly": 1,
    "NRXN3-related_disorder|not_provided": 1,
    "not_provided|NRXN3-related_disorder": 2,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 37,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations": 3,
    "TSHR-related_disorder": 6,
    "Hypothyroidism_due_to_TSH_receptor_mutations": 23,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Inborn_genetic_diseases|not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_specified": 1,
    "Graves_disease|_susceptibility_to|_1|not_specified|not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations": 1,
    "not_provided|Epilepsy|Developmental_delay|autistic_features|not_specified|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations": 1,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided|not_specified": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_provided": 3,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_provided": 14,
    "not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism|TSHR-related_disorder|Inborn_genetic_diseases|Malignant_tumor_of_breast": 1,
    "TSHR-related_disorder|Familial_gestational_hyperthyroidism|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided": 1,
    "not_provided|TSHR-related_disorder": 5,
    "Hypothyroidism_due_to_TSH_receptor_mutations|not_provided|Familial_gestational_hyperthyroidism|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 1,
    "not_specified|not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations": 1,
    "TSHR-related_disorder|Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_provided|Ovarian_cancer": 1,
    "not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism": 2,
    "Hypothyroidism_due_to_TSH_receptor_mutations|not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_specified": 1,
    "TSHR-related_disorder|Familial_gestational_hyperthyroidism": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Familial_gestational_hyperthyroidism|not_provided": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 7,
    "not_provided|Hypothyroidism_due_to_TSH_receptor_mutations": 3,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided|not_specified": 1,
    "Familial_gestational_hyperthyroidism": 3,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|not_specified|not_provided": 2,
    "not_specified|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 2,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_specified|not_provided": 1,
    "not_provided|not_specified|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_provided|not_specified": 1,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_specified|Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided": 1,
    "not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations": 2,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 10,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided": 1,
    "not_provided|Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 1,
    "Thyroid_adenoma|_hyperfunctioning|_somatic": 3,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism|not_provided": 2,
    "TSHR-related_disorder|not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|not_specified": 1,
    "not_provided|TSHR-related_disorder|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 1,
    "not_provided|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 2,
    "not_specified|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|TSHR-related_disorder|not_provided|not_specified": 1,
    "not_provided|TSHR-related_disorder|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations": 1,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|not_provided": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|not_specified": 2,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Inborn_genetic_diseases|not_specified": 1,
    "Smith-Lemli-Opitz_syndrome|Hypothyroidism_due_to_TSH_receptor_mutations": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Congenital_hypothyroidism|Ovarian_cancer|not_provided": 1,
    "not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 1,
    "TSHR-related_disorder|not_provided": 3,
    "Hypothyroidism_due_to_TSH_receptor_mutations|not_provided": 3,
    "Hypothyroidism_due_to_TSH_receptor_mutations|not_provided|not_specified|Ovarian_cancer": 1,
    "not_specified|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|TSHR-related_disorder|not_provided": 1,
    "not_provided|TSHR-related_disorder|Inborn_genetic_diseases|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism": 1,
    "not_provided|Familial_gestational_hyperthyroidism|TSHR-related_disorder|Inborn_genetic_diseases|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 1,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Thyroid_adenoma|_hyperfunctioning|_somatic": 2,
    "THYROID_CARCINOMA_WITH_THYROTOXICOSIS|_SOMATIC": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|not_provided|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 2,
    "Ovarian_cancer|not_specified|not_provided": 1,
    "Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor": 1,
    "Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_specified": 1,
    "Familial_gestational_hyperthyroidism|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|not_provided|not_specified": 1,
    "not_provided|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|TSHR-related_disorder|not_specified": 1,
    "TSHR-related_disorder|Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Hypothyroidism_due_to_TSH_receptor_mutations|Familial_gestational_hyperthyroidism": 1,
    "Familial_hyperthyroidism_due_to_mutations_in_TSH_receptor|Congenital_hypothyroidism": 3,
    "Dandy-Walker_syndrome": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_poor_growth|_dysmorphic_facies|_and_agammaglobulinemia": 1,
    "Galactosylceramide_beta-galactosidase_deficiency": 1022,
    "Galactosylceramide_beta-galactosidase_deficiency|not_provided": 67,
    "Galactosylceramide_beta-galactosidase_deficiency|not_specified": 13,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency": 85,
    "Inborn_genetic_diseases|Galactosylceramide_beta-galactosidase_deficiency": 6,
    "Inborn_genetic_diseases|not_specified|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Abnormal_brain_morphology|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "not_specified|not_provided|See_cases|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|GALC-related_disorder|not_provided": 4,
    "not_specified|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 12,
    "not_specified|Galactosylceramide_beta-galactosidase_deficiency|not_provided": 4,
    "not_specified|Galactosylceramide_beta-galactosidase_deficiency": 9,
    "GALC-related_disorder|Galactosylceramide_beta-galactosidase_deficiency": 4,
    "not_specified|not_provided|Galactosylceramide_beta-galactosidase_deficiency|GALC-related_disorder": 2,
    "GALC-related_disorder|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "not_provided|GALC-related_disorder|Galactosylceramide_beta-galactosidase_deficiency": 3,
    "Galactosylceramide_beta-galactosidase_deficiency|not_specified|not_provided": 7,
    "Galactosylceramide_beta-galactosidase_deficiency|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "not_specified|not_provided|GALC-related_disorder|Galactosylceramide_beta-galactosidase_deficiency": 3,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|not_specified": 5,
    "Galactosylceramide_beta-galactosidase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "GALC-related_disorder|not_specified|not_provided|Galactosylceramide_beta-galactosidase_deficiency": 2,
    "not_provided|not_specified|Galactosylceramide_beta-galactosidase_deficiency|GALC-related_disorder": 2,
    "GALC-related_disorder": 5,
    "not_provided|Inborn_genetic_diseases|Galactosylceramide_beta-galactosidase_deficiency": 2,
    "GALC-related_disorder|Abnormal_brain_morphology|Galactosylceramide_beta-galactosidase_deficiency|not_specified|not_provided": 1,
    "Movement_disorder": 2,
    "not_provided|not_specified|Galactosylceramide_beta-galactosidase_deficiency": 7,
    "Galactosylceramide_beta-galactosidase_deficiency|not_provided|not_specified": 5,
    "not_provided|GALC-related_disorder|Galactosylceramide_beta-galactosidase_deficiency|not_specified": 1,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|Abnormality_of_the_nervous_system": 1,
    "See_cases|Inborn_genetic_diseases|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Inborn_genetic_diseases|Galactosylceramide_beta-galactosidase_deficiency|not_provided": 2,
    "Galactosylceramide_beta-galactosidase_deficiency|Amblyopia|Neonatal_hypoglycemia|EMG_abnormality|Dysmyelinating_leukodystrophy|Small_for_gestational_age|Breech_presentation|EMG:_axonal_abnormality|Leukodystrophy|Loss_of_ambulation|Seizure|Global_developmental_delay|Fetal_growth_restriction|Developmental_regression|Strabismus|Progressive_visual_loss|Nystagmus|Hemiparesis|EEG_abnormality|Status_epilepticus|not_provided": 1,
    "Fabry_disease|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|GALC-related_disorder": 1,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|Spastic_ataxia": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|Incidental_Discovery": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|not_provided|GALC-related_disorder": 2,
    "not_specified|not_provided|Intellectual_disability|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "not_specified|Galactosylceramide_beta-galactosidase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|See_cases|not_specified": 1,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|Leukodystrophy|Fetal_growth_restriction|Global_developmental_delay|Strabismus|Progressive_visual_loss|Amblyopia|Status_epilepticus|Seizure|EEG_abnormality|Nystagmus|Hemiparesis|EMG_abnormality|EMG:_axonal_abnormality|Small_for_gestational_age|Dysmyelinating_leukodystrophy|Breech_presentation|Neonatal_hypoglycemia|Developmental_regression|Loss_of_ambulation": 1,
    "Intellectual_disability|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|Intellectual_disability": 1,
    "not_provided|Galactosylceramide_beta-galactosidase_deficiency|Intellectual_disability|GALC-related_disorder": 1,
    "Galactosylceramide_beta-galactosidase_deficiency|GALC-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|GALC-related_disorder|Galactosylceramide_beta-galactosidase_deficiency": 1,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa": 18,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_3|not_provided": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3": 270,
    "not_provided|Leber_congenital_amaurosis_3": 7,
    "SPATA7-related_disorder|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|not_specified": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_3|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_3": 21,
    "not_specified|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|not_provided": 7,
    "Leber_congenital_amaurosis_3|SPATA7-related_disorder": 3,
    "Leber_congenital_amaurosis_3|not_provided|Retinitis_pigmentosa": 4,
    "Leber_congenital_amaurosis_3|Inborn_genetic_diseases": 11,
    "Leber_congenital_amaurosis_3|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|Inborn_genetic_diseases|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_94|_variable_age_at_onset|SPATA7-related_disorder|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|Inborn_genetic_diseases|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_3": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_3|not_specified|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|Retinal_dystrophy": 4,
    "Leber_congenital_amaurosis|Retinal_dystrophy|not_provided|SPATA7-related_disorder|Leber_congenital_amaurosis_3": 1,
    "not_provided|Leber_congenital_amaurosis_3|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_3|SPATA7-related_disorder|not_provided|not_specified": 1,
    "Leber_congenital_amaurosis_3|Retinal_dystrophy|SPATA7-related_disorder": 1,
    "Leber_congenital_amaurosis_3|not_specified|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_3|not_specified|not_provided|Retinitis_pigmentosa": 2,
    "Leber_congenital_amaurosis_3|SPATA7-related_disorder|not_specified": 1,
    "SPATA7-related_disorder": 2,
    "Leber_congenital_amaurosis_3|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_3": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_3|not_specified": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_3": 3,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_3|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_3|SPATA7-related_disorder|not_specified": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|Inborn_genetic_diseases|not_provided": 1,
    "Retinitis_pigmentosa_94|_variable_age_at_onset|not_specified": 1,
    "Leber_congenital_amaurosis_3|SPATA7-related_disorder|Retinitis_pigmentosa_94|_variable_age_at_onset|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa_94|_variable_age_at_onset|not_provided|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_3|Inborn_genetic_diseases|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_3|not_provided": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Leber_congenital_amaurosis_3": 2,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_3|Retinitis_pigmentosa_94|_variable_age_at_onset|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_3": 2,
    "Retinitis_pigmentosa_94|_variable_age_at_onset|not_provided|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa_94|_variable_age_at_onset": 1,
    "Leber_congenital_amaurosis_3|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Optic_atrophy|not_provided|Leber_congenital_amaurosis_3": 1,
    "SPATA7-related_disorder|not_provided|Leber_congenital_amaurosis_3": 1,
    "Leber_congenital_amaurosis_3|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_3|not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Leber_congenital_amaurosis_3|not_provided": 1,
    "SPATA7-related_disorder|Leber_congenital_amaurosis_3": 1,
    "ZC3H14-related_disorder": 4,
    "Intellectual_disability|_autosomal_recessive_56": 5,
    "not_provided|ZC3H14-related_disorder|not_specified|Intellectual_disability|_autosomal_recessive_56": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_56": 1,
    "not_specified|ZC3H14-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_56|not_specified": 1,
    "ZC3H14-related_disorder|not_specified": 1,
    "ZC3H14-related_disorder|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_56": 2,
    "not_provided|ZC3H14-related_disorder": 1,
    "ZC3H14-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa": 10,
    "TTC8-related_disorder": 54,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_8|TTC8-related_disorder": 1,
    "TTC8-related_disorder|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome": 4,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome": 8,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8": 7,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|TTC8-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa|Bardet-Biedl_syndrome_8|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome": 4,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 26,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 7,
    "Bardet-Biedl_syndrome_8": 13,
    "TTC8-related_disorder|Bardet-Biedl_syndrome": 15,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|TTC8-related_disorder": 2,
    "TTC8-related_disorder|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 1,
    "Retinitis_pigmentosa_51": 20,
    "TTC8-related_disorder|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome|TTC8-related_disorder|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 3,
    "Retinitis_pigmentosa_51|Retinal_dystrophy": 1,
    "not_provided|Bardet-Biedl_syndrome_8": 2,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|TTC8-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|not_specified": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome": 2,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|TTC8-related_disorder": 1,
    "Bardet-Biedl_syndrome|not_provided|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Retinal_dystrophy": 1,
    "TTC8-related_disorder|not_specified|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa|Bardet-Biedl_syndrome_8|TTC8-related_disorder": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8": 2,
    "Bardet-Biedl_syndrome|TTC8-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|TTC8-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|TTC8-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa": 1,
    "TTC8-related_disorder|Bardet-Biedl_syndrome|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8": 2,
    "TTC8-related_disorder|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8": 1,
    "TTC8-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome": 2,
    "TTC8-related_disorder|not_provided|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome|TTC8-related_disorder": 15,
    "not_provided|TTC8-related_disorder|Bardet-Biedl_syndrome": 1,
    "TTC8-related_disorder|not_specified|Retinal_dystrophy|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Retinitis_pigmentosa|Bardet-Biedl_syndrome": 1,
    "TTC8-related_disorder|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 1,
    "Bardet-Biedl_syndrome|not_specified|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|TTC8-related_disorder": 1,
    "TTC8-related_disorder|Bardet-Biedl_syndrome|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|not_provided": 1,
    "TTC8-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|TTC8-related_disorder|Truncal_obesity|Postaxial_foot_polydactyly|Intellectual_disability|_moderate|not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8": 3,
    "not_specified|TTC8-related_disorder": 2,
    "Bardet-Biedl_syndrome_8|not_provided": 1,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|TTC8-related_disorder": 1,
    "not_provided|TTC8-related_disorder": 1,
    "Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome_8|not_specified": 1,
    "Retinitis_pigmentosa_51|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "not_specified|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|not_provided|Bardet-Biedl_syndrome": 1,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome|TTC8-related_disorder": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_51": 3,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|not_provided|Bardet-Biedl_syndrome": 2,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Retinitis_pigmentosa|TTC8-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|TTC8-related_disorder|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|TTC8-related_disorder|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|Retinitis_pigmentosa_51|TTC8-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|TTC8-related_disorder|Retinitis_pigmentosa_51": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|Bardet-Biedl_syndrome": 1,
    "TTC8-related_disorder|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|not_provided|TTC8-related_disorder": 1,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|TTC8-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|TTC8-related_disorder|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|TTC8-related_disorder": 1,
    "not_specified|Bardet-Biedl_syndrome_8|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Inborn_genetic_diseases": 1,
    "TTC8-related_disorder|Inborn_genetic_diseases": 2,
    "TTC8-related_disorder|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_8": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|TTC8-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|TTC8-related_disorder": 2,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|TTC8-related_disorder|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51": 1,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|Inborn_genetic_diseases|Retinitis_pigmentosa|Macular_dystrophy|Bardet-Biedl_syndrome|TTC8-related_disorder": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis|Bardet-Biedl_syndrome": 1,
    "TTC8-related_disorder|Inborn_genetic_diseases|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8": 1,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa_51|not_provided": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|TTC8-related_disorder": 1,
    "Retinitis_pigmentosa_51|Bardet-Biedl_syndrome_8|TTC8-related_disorder|Bardet-Biedl_syndrome": 1,
    "TTC8-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_8": 1,
    "Bardet-Biedl_syndrome_8|Bardet-Biedl_syndrome|not_specified|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_51|TTC8-related_disorder|not_specified": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_8": 1,
    "Bardet-Biedl_syndrome|TTC8-related_disorder|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_8": 4,
    "Bardet-Biedl_syndrome_8|Retinitis_pigmentosa|not_provided": 1,
    "not_provided|Bardet-Biedl_syndrome_8|Retinitis_pigmentosa": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1": 54,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1": 15,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|not_provided": 5,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|not_specified": 10,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|not_provided": 2,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|not_specified": 2,
    "not_specified|TDP1-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|not_provided|not_specified": 2,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|TDP1-related_disorder|not_specified": 1,
    "Spinocerebellar_ataxia|_autosomal_recessive|_with_axonal_neuropathy_1|not_specified|TDP1-related_disorder|not_provided": 1,
    "TDP1-related_disorder": 2,
    "Neurodevelopmental_disorder_with_poor_growth|_spastic_tetraplegia|_and_hearing_loss": 1,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14": 2,
    "not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_4": 2,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14": 32,
    "Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4": 45,
    "Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|not_provided|not_specified": 1,
    "Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Cardiovascular_phenotype": 3,
    "not_provided|Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Cardiovascular_phenotype": 1,
    "not_specified|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14": 1,
    "Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|not_specified": 3,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14": 5,
    "Cardiovascular_phenotype|Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|not_provided": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_4|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14|not_provided": 1,
    "Long_QT_syndrome_14": 4,
    "CALM1-related_disorder|Cardiovascular_phenotype|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia|Catecholaminergic_polymorphic_ventricular_tachycardia_1": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|CALM1-related_disorder": 1,
    "Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|CALM1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_14|not_provided": 1,
    "Long_QT_syndrome_14|Catecholaminergic_polymorphic_ventricular_tachycardia_4|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Catecholaminergic_polymorphic_ventricular_tachycardia_4|Long_QT_syndrome_14": 1,
    "not_specified|RPS6KA5-related_disorder": 1,
    "Amelogenesis_imperfecta|_hypomaturation_type|_IIa6|not_provided": 1,
    "Amelogenesis_imperfecta|_hypomaturation_type|_IIa6": 1,
    "GPR68-related_disorder": 8,
    "Amelogenesis_imperfecta|_hypomaturation_type|_IIa6|Amelogenesis_imperfecta": 3,
    "CCDC88C-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_40": 1,
    "not_provided|Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 8,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|Inborn_genetic_diseases|not_provided": 1,
    "CCDC88C-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|not_specified": 2,
    "not_specified|CCDC88C-related_disorder|not_provided": 2,
    "CCDC88C-related_disorder|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|not_specified|not_provided": 1,
    "not_specified|Intellectual_disability|Inborn_genetic_diseases|not_provided": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Congenital_hydrocephalus": 1,
    "Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided": 3,
    "Spinocerebellar_ataxia_type_40": 9,
    "CCDC88C-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|CCDC88C-related_disorder": 19,
    "CCDC88C-related_disorder|not_provided": 19,
    "Inborn_genetic_diseases|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 3,
    "CCDC88C-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided": 3,
    "Hydrocephalus|CCDC88C-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_40|not_provided": 1,
    "Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 26,
    "Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided|Inborn_genetic_diseases": 1,
    "CCDC88C-related_disorder": 7,
    "not_specified|not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40": 2,
    "Inborn_genetic_diseases|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CCDC88C-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "not_specified|not_provided|CCDC88C-related_disorder|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40": 2,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|not_specified|not_provided": 1,
    "not_specified|not_provided|CCDC88C-related_disorder|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|Inborn_genetic_diseases": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_specified|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_specified": 1,
    "CCDC88C-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|CCDC88C-related_disorder|Epilepsy|Intellectual_disability": 1,
    "Hydrocephalus": 1,
    "not_provided|not_specified|CCDC88C-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|not_provided": 3,
    "Spinocerebellar_ataxia_type_40|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40": 2,
    "not_provided|Spinocerebellar_ataxia_type_40": 1,
    "not_specified|CCDC88C-related_disorder|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CCDC88C-related_disorder|not_specified": 1,
    "not_specified|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Spinocerebellar_ataxia_type_40|Inborn_genetic_diseases": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_40|not_provided": 1,
    "Spinocerebellar_ataxia_type_40|not_specified|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Inborn_genetic_diseases": 1,
    "CCDC88C-related_disorder|Intellectual_disability|not_provided": 1,
    "Spinocerebellar_ataxia_type_40|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CCDC88C-related_disorder|not_provided": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|not_provided|Spinocerebellar_ataxia_type_40|not_specified": 1,
    "Cutis_laxa|Macular_degeneration|_age-related|_3": 15,
    "Macular_degeneration|_age-related|_3|Cutis_laxa": 12,
    "Macular_degeneration|_age-related|_3|Cutis_laxa|not_provided": 6,
    "not_provided|Macular_degeneration|_age-related|_3|Cutis_laxa": 4,
    "Cutis_laxa|_autosomal_dominant_2|not_provided": 2,
    "Macular_degeneration|_age-related|_3|Cutis_laxa|not_specified|not_provided": 2,
    "Macular_degeneration|_age-related|_3|not_provided|Age-related_macular_degeneration": 1,
    "not_specified|FBLN5-related_disorder|not_provided": 1,
    "Macular_degeneration|_age-related|_3|Cutis_laxa|_autosomal_dominant_2|Cutis_laxa|_autosomal_recessive|_type_1A": 1,
    "Cutis_laxa|not_provided|not_specified|Macular_degeneration|_age-related|_3": 1,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_dominant_2|Macular_degeneration|_age-related|_3": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_dominant": 1,
    "Cutis_laxa|_autosomal_recessive|_type_1A": 4,
    "Cutis_laxa|_autosomal_dominant_2": 2,
    "Macular_degeneration|_age-related|_3|not_specified|Cutis_laxa|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H|Hereditary_sensorimotor_neuropathy_with_hyperelastic_skin": 1,
    "Cutis_laxa|not_provided|Macular_degeneration|_age-related|_3": 1,
    "not_provided|FBLN5-related_disorder": 3,
    "Macular_degeneration|_age-related|_3|Age-related_macular_degeneration|not_provided": 2,
    "FBLN5-related_disorder|not_provided|not_specified": 1,
    "not_provided|FBLN5-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Cutis_laxa|_autosomal_recessive|_type_1A|Macular_degeneration|_age-related|_3|Cutis_laxa|_autosomal_dominant_2|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H": 1,
    "Macular_degeneration|_age-related|_3|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H|Cutis_laxa|_autosomal_dominant_2|Cutis_laxa|_autosomal_recessive|_type_1A|not_provided|Age-related_macular_degeneration|not_specified|Cutis_laxa|See_cases": 1,
    "not_provided|Macular_degeneration|_age-related|_3|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H": 1,
    "not_specified|not_provided|Cutis_laxa|Macular_degeneration|_age-related|_3": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H": 2,
    "not_provided|Cutis_laxa|Macular_degeneration|_age-related|_3|Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_dominant_2|not_specified": 1,
    "Age_related_macular_degeneration_1|Autosomal_recessive_cutis_laxa_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Optic_atrophy|Cutis_laxa|Cutis_laxa|_autosomal_dominant|Macular_degeneration|_age-related|_3": 1,
    "FBLN5-related_disorder|not_provided": 7,
    "Peripheral_axonal_neuropathy|not_provided": 1,
    "not_provided|not_specified|Cutis_laxa|Macular_degeneration|_age-related|_3": 1,
    "Cutis_laxa|_autosomal_dominant|not_provided": 1,
    "Cutis_laxa|_autosomal_dominant_2|Cutis_laxa|_autosomal_recessive|_type_1A|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H|Macular_degeneration|_age-related|_3|not_provided": 1,
    "not_provided|Age-related_macular_degeneration|Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_dominant_2|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H|Macular_degeneration|_age-related|_3": 1,
    "Cutis_laxa|_autosomal_dominant|Cutis_laxa|_autosomal_recessive|_type_1A": 3,
    "not_provided|Inborn_genetic_diseases|FBLN5-related_disorder": 1,
    "Macular_degeneration|_age-related|_3|FBLN5-related_disorder|not_provided|Cutis_laxa": 1,
    "Cutis_laxa|FBLN5-related_disorder|not_specified|not_provided|Macular_degeneration|_age-related|_3": 1,
    "Cutis_laxa|Cutis_laxa|_autosomal_recessive|_type_1A|not_provided|Cutis_laxa|_autosomal_dominant|Macular_degeneration|_age-related|_3": 1,
    "Cutis_laxa|Macular_degeneration|_age-related|_3|not_provided": 1,
    "Macular_degeneration|_age-related|_3|Age-related_macular_degeneration": 2,
    "not_provided|FBLN5-related_disorder|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H|Cutis_laxa|_autosomal_dominant_2|Cutis_laxa|_autosomal_recessive|_type_1A|Macular_degeneration|_age-related|_3|FBLN5-related_disorder|Cutis_laxa|not_specified|not_provided": 1,
    "Age-related_macular_degeneration": 1,
    "Cutis_laxa|Macular_degeneration|_age-related|_3|not_provided|FBLN5-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H|Cutis_laxa|_autosomal_dominant_2|Cutis_laxa|_autosomal_recessive|_type_1A|Macular_degeneration|_age-related|_3|Hereditary_sensorimotor_neuropathy_with_hyperelastic_skin|Cutis_laxa|Retinal_dystrophy|not_provided|Optic_atrophy": 1,
    "FBLN5-related_disorder": 3,
    "Macular_degeneration|_age-related|_3|Cutis_laxa|_autosomal_recessive|_type_1A|Cutis_laxa|_autosomal_dominant_2|Charcot-Marie-Tooth_disease|_demyelinating|_IIA_1H": 1,
    "not_provided|Macular_degeneration|Cutis_Laxa|_Dominant/Recessive|Inborn_genetic_diseases|Retinal_dystrophy|not_specified": 1,
    "Macular_degeneration|_age-related|_3|not_provided|FBLN5-related_disorder|Age-related_macular_degeneration": 1,
    "Age-related_macular_degeneration|Cutis_laxa|_autosomal_dominant_2|not_provided": 1,
    "not_specified|Macular_degeneration|Cutis_Laxa|_Dominant/Recessive": 1,
    "Cutis_Laxa|_Dominant/Recessive|not_provided|Macular_degeneration": 1,
    "Achondrogenesis|_type_IA|not_provided": 27,
    "Achondrogenesis|_type_IA": 467,
    "Achondrogenesis": 6,
    "not_provided|Achondrogenesis|_type_IA": 19,
    "not_provided|Connective_tissue_disorder|Achondrogenesis|_type_IA": 4,
    "not_provided|Achondrogenesis|_type_IA|TRIP11-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Achondrogenesis|_type_IA": 1,
    "Achondrogenesis|_type_IA|Connective_tissue_disorder|not_specified|not_provided": 9,
    "not_specified|not_provided|Achondrogenesis|_type_IA": 1,
    "not_provided|Achondrogenesis|_type_IA|Inborn_genetic_diseases": 3,
    "TRIP11-related_disorder|Achondrogenesis|_type_IA|Connective_tissue_disorder|not_specified|not_provided": 1,
    "TRIP11-related_disorder|Connective_tissue_disorder|not_provided|Achondrogenesis|_type_IA": 1,
    "TRIP11-related_disorder|Connective_tissue_disorder|Achondrogenesis|_type_IA|not_provided": 1,
    "not_provided|Odontochondrodysplasia_1|not_specified|Achondrogenesis|_type_IA": 1,
    "Odontochondrodysplasia_1|Achondrogenesis|_type_IA": 5,
    "Odontochondrodysplasia_1": 12,
    "Achondrogenesis|_type_IA|Inborn_genetic_diseases": 18,
    "Achondrogenesis|_type_IA|TRIP11-related_disorder": 4,
    "not_provided|not_specified|TRIP11-related_disorder|Achondrogenesis|_type_IA": 1,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IA": 23,
    "not_provided|Odontochondrodysplasia_1|Achondrogenesis|_type_IA": 1,
    "not_specified|Connective_tissue_disorder|Achondrogenesis|_type_IA|not_provided": 1,
    "Achondrogenesis|_type_IA|not_provided|Inborn_genetic_diseases|TRIP11-related_disorder": 2,
    "Connective_tissue_disorder|Inborn_genetic_diseases|not_provided|Achondrogenesis|_type_IA": 1,
    "Connective_tissue_disorder|TRIP11-related_disorder|not_provided|Achondrogenesis|_type_IA": 1,
    "Achondrogenesis|_type_IA|not_specified|not_provided": 4,
    "not_specified|Achondrogenesis|_type_IA": 3,
    "Achondrogenesis|_type_IA|not_specified": 2,
    "Inborn_genetic_diseases|TRIP11-related_disorder": 1,
    "not_provided|TRIP11-related_disorder|Achondrogenesis|_type_IA": 2,
    "Achondrogenesis|_type_IA|Odontochondrodysplasia_1": 4,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IA|Odontochondrodysplasia_1": 2,
    "not_provided|Achondrogenesis|_type_IA|Odontochondrodysplasia_1": 1,
    "Connective_tissue_disorder|not_provided|not_specified|Achondrogenesis|_type_IA": 1,
    "Achondrogenesis|_type_IA|Inborn_genetic_diseases|not_provided": 3,
    "Achondrogenesis|_type_IA|not_specified|Inborn_genetic_diseases": 1,
    "Achondrogenesis|_type_IA|not_provided|TRIP11-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Achondrogenesis|_type_IA": 1,
    "TRIP11-related_disorder": 2,
    "TRIP11-related_disorder|Achondrogenesis|_type_IA|Inborn_genetic_diseases": 2,
    "not_specified|Achondrogenesis|_type_IA|not_provided": 1,
    "Inborn_genetic_diseases|Connective_tissue_disorder|not_specified|not_provided|Achondrogenesis|_type_IA|TRIP11-related_disorder": 1,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IA|not_specified": 1,
    "Connective_tissue_disorder|Achondrogenesis|_type_IA|not_specified|not_provided": 8,
    "TRIP11-related_disorder|not_specified|Achondrogenesis|_type_IA": 2,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IA|not_provided": 1,
    "TRIP11-related_skeletal_dysplasia": 1,
    "Achondrogenesis|_type_IA|Odontochondrodysplasia_1|not_provided|Connective_tissue_disorder|not_specified": 1,
    "Connective_tissue_disorder|not_provided|Achondrogenesis|_type_IA": 2,
    "Achondrogenesis|_type_IA|Connective_tissue_disorder": 3,
    "TRIP11-related_disorder|Achondrogenesis|_type_IA|not_provided": 1,
    "Odontochondrodysplasia_1|not_provided|Achondrogenesis|_type_IA": 1,
    "not_provided|Achondrogenesis|_type_IA|Connective_tissue_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Achondrogenesis|_type_IA|TRIP11-related_disorder|not_provided": 1,
    "Achondrogenesis|_type_IA|Odontochondrodysplasia_1|not_provided": 1,
    "Connective_tissue_disorder|Achondrogenesis|_type_IA|not_provided": 1,
    "Achondrogenesis|_type_IA|not_provided|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "TRIP11-related_disorder|Achondrogenesis|_type_IA": 2,
    "TRIP11-related_disorder|not_provided|Achondrogenesis|_type_IA": 1,
    "TRIP11-related_disorder|Connective_tissue_disorder|Achondrogenesis|_type_IA|not_specified|not_provided": 1,
    "TRIP11-related_disorder|Connective_tissue_disorder|Achondrogenesis|_type_IA|Odontochondrodysplasia_1|not_specified|not_provided": 1,
    "ATXN3-related_disorder|Azorean_disease|not_specified|not_provided": 1,
    "Azorean_disease": 4,
    "ATXN3-related_disorder|not_specified": 1,
    "ATXN3-related_disorder|not_specified|not_provided|Azorean_disease": 1,
    "ATXN3-related_disorder": 4,
    "ATXN3-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|ATXN3-related_disorder": 1,
    "not_specified|ATXN3-related_disorder|not_provided": 1,
    "ATXN3-related_disorder|Tip-toe_gait": 1,
    "ATXN3-related_disorder|not_specified|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_6|_BLOND/BROWN_HAIR": 1,
    "not_provided|SLC24A4-related_disorder": 3,
    "Amelogenesis_imperfecta_hypomaturation_type_2A5": 5,
    "SLC24A4-related_disorder": 7,
    "SLC24A4-related_disorder|Inborn_genetic_diseases": 1,
    "SLC24A4-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|SLC24A4-related_disorder": 1,
    "not_provided|RIN3-related_disorder": 1,
    "RIN3-related_disorder": 2,
    "Dysostosis_multiplex|_Ain-Naz_type": 2,
    "LYSET-related_disorder": 1,
    "GON7-related_disorder": 4,
    "Galloway-Mowat_syndrome|Galloway-Mowat_syndrome_9": 1,
    "Galloway-Mowat_syndrome_9": 1,
    "Galloway-Mowat_syndrome": 2,
    "Li-Campeau_syndrome": 9,
    "UNC79-related_disorder": 18,
    "UNC79-related_disorder|not_provided": 3,
    "UNC79-associated_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|UNC79-related_disorder": 1,
    "UNC79-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Familial_sleep-related_hypermotor_epilepsy|not_specified": 6,
    "not_specified|Familial_sleep-related_hypermotor_epilepsy": 4,
    "not_provided|Familial_sleep-related_hypermotor_epilepsy": 4,
    "Familial_sleep-related_hypermotor_epilepsy|PRIMA1-related_disorder": 1,
    "PRIMA1-related_disorder": 1,
    "PRIMA1-related_disorder|Familial_sleep-related_hypermotor_epilepsy": 1,
    "not_provided|Familial_sleep-related_hypermotor_epilepsy|PRIMA1-related_disorder": 1,
    "not_provided|Venous_thrombosis|_susceptibility_to": 1,
    "SERPINA6-related_disorder|Corticosteroid-binding_globulin_deficiency": 1,
    "SERPINA6-related_disorder": 5,
    "Corticosteroid-binding_globulin_deficiency|not_provided": 1,
    "not_provided|SERPINA6-related_disorder": 1,
    "Corticosteroid-binding_globulin_deficiency": 4,
    "Corticosteroid-binding_globulin_deficiency|Inborn_genetic_diseases": 1,
    "SERPINA6-related_disorder|not_provided": 1,
    "not_specified|Corticosteroid-binding_globulin_deficiency|SERPINA6-related_disorder|not_provided": 1,
    "not_provided|Alpha-1-antitrypsin_deficiency": 18,
    "Alpha-1-antitrypsin_deficiency": 282,
    "Alpha-1-antitrypsin_deficiency|not_provided|PI_KALSHEKER-POLLER": 1,
    "Alpha-1-antitrypsin_deficiency|not_provided": 11,
    "SERPINA1-related_disorder": 24,
    "Alpha-1-antitrypsin_deficiency|SERPINA1-related_disorder": 11,
    "SERPINA1-related_disorder|Alpha-1-antitrypsin_deficiency": 7,
    "not_provided|Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency": 1,
    "Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency|PI_M3|not_provided|not_specified": 1,
    "SERPINA1-related_disorder|Alpha-1-antitrypsin_deficiency|not_provided|PI_M(HEERLEN)|Inborn_genetic_diseases": 1,
    "SERPINA1-related_disorder|not_provided|Alpha-1-antitrypsin_deficiency": 5,
    "not_provided|Alpha-1-antitrypsin_deficiency|PI_CHRISTCHURCH|SERPINA1-related_disorder": 1,
    "Alpha-1-antitrypsin_deficiency|PI_NULL(BOLTON)|PI_Q0(BOLTON)": 1,
    "Alpha-1-antitrypsin_deficiency|Hemorrhagic_disease_due_to_alpha-1-antitrypsin_Pittsburgh_mutation": 1,
    "PI_NULL(MATTAWA)": 1,
    "Alpha-1-antitrypsin_deficiency|Inborn_genetic_diseases": 5,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)|Neurodevelopmental_disorder|SERPINA1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Alpha-1-antitrypsin_deficiency|Chronic_obstructive_pulmonary_disease|PI_Z(AUGSBURG)|PI_Z(TUN)|PI_Z|FRAXE|See_cases": 1,
    "Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency": 2,
    "Alpha-1-antitrypsin_deficiency|not_specified|not_provided": 1,
    "PI_P(ST._ALBANS)|Alpha-1-antitrypsin_deficiency|not_specified|SERPINA1-related_disorder": 1,
    "not_provided|Alpha-1-antitrypsin_deficiency|PI_W(BETHESDA)": 1,
    "Hereditary_angioedema_with_normal_C1Inh|not_provided": 1,
    "not_specified|Alpha-1-antitrypsin_deficiency": 2,
    "SERPINA1-related_disorder|not_provided": 4,
    "Alpha-1-antitrypsin_deficiency|PI_NULL(HONG_KONG_1)|PI_Q0(HONG_KONG_1)": 1,
    "Inborn_genetic_diseases|SERPINA1-related_disorder": 1,
    "Alpha-1-antitrypsin_deficiency|Inborn_genetic_diseases|SERPINA1-related_disorder": 1,
    "SERPINA1-related_disorder|not_provided|Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency": 1,
    "SERPINA1-related_disorder|not_specified|not_provided|Alpha-1-antitrypsin_deficiency": 1,
    "Alpha-1-antitrypsin_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Alpha-1-antitrypsin_deficiency|not_provided|not_specified": 1,
    "not_provided|Alpha-1-antitrypsin_deficiency|SERPINA1-related_disorder": 2,
    "Susceptibility_to_severe_coronavirus_disease_(COVID-19)|SERPINA1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Alpha-1-antitrypsin_deficiency|Chronic_obstructive_pulmonary_disease|PI_S|Cystic_fibrosis": 1,
    "Squamous_cell_carcinoma|not_specified": 1,
    "not_provided|not_specified|Alpha-1-antitrypsin_deficiency": 1,
    "SERPINA1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_21|not_provided|Alpha-1-antitrypsin_deficiency|PI_P(DUARTE)|PI_P(LOWELL)|PI_NULL(CARDIFF)|PI_Q0(CARDIFF)": 1,
    "SERPINA1-related_disorder|Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency": 1,
    "not_specified|not_provided|Alpha-1-antitrypsin_deficiency": 1,
    "SERPINA1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Alpha-1-antitrypsin_deficiency|PI_F": 1,
    "Alpha-1-antitrypsin_deficiency|PI_Q0(BELLINGHAM)|PI_NULL(BELLINGHAM)|not_provided": 1,
    "SERPINA1-related_disorder|Alpha-1-antitrypsin_deficiency|not_provided": 2,
    "Inborn_genetic_diseases|PI_M1-ALA213|PI|_M1V": 1,
    "Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency|PI_M1-ALA213|PI|_M1A|not_provided|not_specified": 1,
    "Alpha-1-antitrypsin_deficiency|not_provided|PI_X": 1,
    "Alpha-1-antitrypsin_deficiency|PI_NULL(WEST)|not_provided": 1,
    "Alpha-1-antitrypsin_deficiency|PI_Q0(GRANITE_FALLS)": 1,
    "not_provided|Inborn_genetic_diseases|SERPINA1-related_disorder|Alpha-1-antitrypsin_deficiency": 1,
    "not_provided|Alpha-1-antitrypsin_deficiency|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency|not_specified|not_provided": 2,
    "not_provided|SERPINA1-related_disorder": 1,
    "Alpha-1-antitrypsin_deficiency|PI_NULL(DEVON)|PI_Q0(DEVON)|PI_NULL(NEWPORT)|PI_Q0(NEWPORT)": 1,
    "Alpha-1-antitrypsin_deficiency|not_provided|not_specified|PI_M4|PI_M2|Inborn_genetic_diseases": 1,
    "PI_Q0(LUDWIGSHAFEN)|PI_NULL(LUDWIGSHAFEN)|Alpha-1-antitrypsin_deficiency": 1,
    "Alpha-1-antitrypsin_deficiency|PI_Z(BRISTOL)|not_provided": 1,
    "Alpha-1-antitrypsin_deficiency|PI_M(MINERAL_SPRINGS)": 1,
    "Alpha-1-antitrypsin_deficiency|PI_S(IIYAMA)": 1,
    "SERPINA1-related_disorder|not_provided|PI_M(MALTON)|Alpha-1-antitrypsin_deficiency": 1,
    "Alpha-1-antitrypsin_deficiency|SERPINA1-related_disorder|not_provided": 1,
    "not_provided|Alpha-1-antitrypsin_deficiency|PI_M(PROCIDA)|See_cases": 1,
    "SERPINA1-related_disorder|not_provided|Alpha-1-antitrypsin_deficiency|PI_I": 1,
    "PI_V(MUNICH)|Alpha-1-antitrypsin_deficiency": 1,
    "Inborn_genetic_diseases|Alpha-1-antitrypsin_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|SERPINA1-related_disorder|not_provided|Alpha-1-antitrypsin_deficiency": 1,
    "Alpha-1-antitrypsin_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Alpha-1-antitrypsin_deficiency|PI_Z(WREXHAM)": 1,
    "Pericardial_effusion|Pleural_effusion": 1,
    "Hereditary_palmoplantar_keratoderma|_Gamborg-Nielsen_type": 1,
    "not_provided|Hereditary_palmoplantar_keratoderma|_Gamborg-Nielsen_type": 1,
    "SERPINA3-related_disorder": 7,
    "ANTICHYMOTRYPSIN_SIGNAL_PEPTIDE_POLYMORPHISM|not_specified|SERPINA3-related_disorder|not_provided": 1,
    "not_provided|SERPINA3-related_disorder": 3,
    "ANTICHYMOTRYPSIN_BOCHUM_1": 1,
    "Antichymotrypsin_deficiency-alpha-1|not_specified": 1,
    "SERPINA3-related_disorder|not_provided|not_specified": 1,
    "SERPINA3-related_disorder|not_provided": 1,
    "Antichymotrypsin_deficiency-alpha-1|ANTICHYMOTRYPSIN_BONN_1|SERPINA3-related_disorder|not_provided": 1,
    "not_provided|SERPINA3-related_disorder|not_specified": 1,
    "ANTICHYMOTRYPSIN_ISEHARA_1|Peripheral_arterial_occlusive_disease_1": 1,
    "not_provided|ANTICHYMOTRYPSIN_ISEHARA_2": 1,
    "Short_stature-auditory_canal_atresia-mandibular_hypoplasia-skeletal_anomalies_syndrome": 4,
    "GSC-related_disorder": 1,
    "GSC-related_disorder|not_provided": 2,
    "Short_stature-auditory_canal_atresia-mandibular_hypoplasia-skeletal_anomalies_syndrome|not_provided": 1,
    "DICER1-related_tumor_predisposition": 2622,
    "not_provided|DICER1-related_tumor_predisposition": 37,
    "Pleuropulmonary_blastoma": 20,
    "DICER1-related_tumor_predisposition|not_provided": 34,
    "not_provided|Pleuropulmonary_blastoma": 1,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition": 2,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1055,
    "DICER1-related_tumor_predisposition|not_provided|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|DICER1-related_disorder": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 19,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 857,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|DICER1-related_disorder": 5,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 48,
    "Euthyroid_goiter|DICER1-related_tumor_predisposition|Rhabdomyosarcoma|_embryonal|_2|Hereditary_cancer-predisposing_syndrome|not_provided|Pleuropulmonary_blastoma": 1,
    "DICER1-related_tumor_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome": 6,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 12,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified": 22,
    "DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 32,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|DICER1-related_tumor_predisposition": 3,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 36,
    "not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 9,
    "DICER1-related_disorder|not_specified|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 7,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 3,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided": 34,
    "Euthyroid_goiter|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|not_specified": 21,
    "not_specified|not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 6,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|DICER1-related_tumor_predisposition": 3,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|not_specified|DICER1-related_tumor_predisposition": 1,
    "Cancer_or_benign_tumor|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition|not_specified|not_provided": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma": 2,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 19,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 38,
    "Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition": 28,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 15,
    "Euthyroid_goiter|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma": 1,
    "DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 3,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|not_provided": 1,
    "Pleuropulmonary_blastoma|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition": 1,
    "Supratentorial_primitive_neuroectodermal_tumor|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma": 1,
    "not_specified|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 7,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|not_specified": 3,
    "DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma": 4,
    "Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "not_specified|not_provided|DICER1-related_tumor_predisposition": 5,
    "DICER1-related_tumor_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "Rhabdomyosarcoma|_embryonal|_2": 2,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified|not_provided": 3,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_tumor_predisposition": 11,
    "Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided|not_specified": 2,
    "not_specified|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|DICER1-related_tumor_predisposition|DICER1-related_disorder": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 9,
    "DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Euthyroid_goiter|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Euthyroid_goiter": 4,
    "Pineoblastoma|not_provided|DICER1-related_tumor_predisposition": 2,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "not_provided|not_specified|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified": 8,
    "DICER1-related_tumor_predisposition|Rhabdomyosarcoma|_embryonal|_2": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder": 10,
    "not_provided|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 23,
    "Diffuse_midline_glioma|_H3_K27-altered|DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Euthyroid_goiter|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|DICER1-related_disorder|not_provided": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_disorder|not_specified|not_provided": 1,
    "DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition": 5,
    "DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_specified|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Ovarian_cancer": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_provided": 5,
    "Pleuropulmonary_blastoma|Euthyroid_goiter": 1,
    "DICER1-related_disorder|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 29,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|not_specified|not_provided": 1,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pineoblastoma|DICER1-related_tumor_predisposition": 1,
    "not_provided|DICER1-related_tumor_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition|not_provided": 1,
    "Neurodevelopmental_disorder|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|not_provided|DICER1-related_tumor_predisposition|not_specified": 1,
    "Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 2,
    "Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 3,
    "Pediatric_high-grade_glioma|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|DICER1-related_tumor_predisposition": 2,
    "Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 27,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pleuropulmonary_blastoma": 2,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 2,
    "DICER1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 3,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided|Pleuropulmonary_blastoma": 1,
    "DICER1-related_tumor_predisposition|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer": 1,
    "Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "Pineoblastoma|not_provided|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma": 1,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 4,
    "Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided": 3,
    "Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided": 1,
    "Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition": 2,
    "not_provided|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter": 1,
    "DICER1-related_tumor_predisposition|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified|not_provided|Pleuropulmonary_blastoma": 1,
    "not_provided|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_tumor_predisposition": 1,
    "not_specified|DICER1-related_tumor_predisposition": 12,
    "DICER1-related_disorder": 6,
    "not_specified|DICER1-related_tumor_predisposition|DICER1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition|not_specified": 2,
    "not_specified|DICER1-related_tumor_predisposition|Euthyroid_goiter|not_provided": 1,
    "DICER1-related_tumor_predisposition|not_specified|not_provided": 3,
    "Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_specified": 1,
    "DICER1-related_tumor_predisposition|not_specified|not_provided|Euthyroid_goiter": 1,
    "DICER1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_tumor_predisposition": 1,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|not_specified|DICER1-related_tumor_predisposition|not_provided": 1,
    "DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified": 1,
    "Pleuropulmonary_blastoma|not_specified|DICER1-related_tumor_predisposition|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided": 1,
    "Euthyroid_goiter|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2": 1,
    "Pleuropulmonary_blastoma|not_specified|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided": 1,
    "not_specified|not_provided|DICER1-related_disorder|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "Euthyroid_goiter|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 3,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pineoblastoma|DICER1-related_tumor_predisposition": 1,
    "not_provided|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 2,
    "not_provided|Euthyroid_goiter": 1,
    "DICER1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "Euthyroid_goiter|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|DICER1-related_tumor_predisposition": 1,
    "Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter": 2,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|DICER1-related_tumor_predisposition": 1,
    "Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|DICER1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 2,
    "not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|High-grade_astrocytoma_with_piloid_features|Childhood_kidney_cell_carcinoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_provided": 1,
    "Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 2,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder": 1,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|not_provided": 1,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified|not_provided": 1,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 2,
    "not_specified|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter": 1,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|DICER1-related_tumor_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 2,
    "Pleuropulmonary_blastoma|not_specified|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|DICER1-related_tumor_predisposition": 1,
    "not_specified|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "Ovarian_cancer|not_provided|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter": 2,
    "Pleuropulmonary_blastoma|not_specified|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "not_specified|not_provided|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Euthyroid_goiter": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_tumor_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|not_provided|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 3,
    "Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 3,
    "Pleuropulmonary_blastoma|not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|not_provided": 1,
    "DICER1-related_tumor_predisposition|not_provided|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_specified": 1,
    "DICER1-related_tumor_predisposition|not_provided|not_specified": 2,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition|DICER1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Euthyroid_goiter": 1,
    "DICER1-related_tumor_predisposition|See_cases": 1,
    "Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition": 1,
    "not_specified|DICER1-related_tumor_predisposition|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_specified": 1,
    "Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition|not_provided": 1,
    "Euthyroid_goiter|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "DICER1-related_tumor_predisposition|not_specified|not_provided|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2": 1,
    "not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_disorder|not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "DICER1-related_tumor_predisposition|Anophthalmia-microphthalmia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "DICER1-related_tumor_predisposition|Ovarian_cancer": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2": 1,
    "not_specified|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Rhabdomyosarcoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2": 1,
    "DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided": 1,
    "DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|DICER1-related_tumor_predisposition|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma|not_provided|not_specified|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition|DICER1-related_disorder": 1,
    "Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_disorder|DICER1-related_tumor_predisposition": 1,
    "Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|DICER1-related_disorder": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma": 2,
    "Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Pleuropulmonary_blastoma|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Pleuropulmonary_blastoma": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter": 1,
    "not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Pineoblastoma|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 3,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|DICER1-related_disorder|Pleuropulmonary_blastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|DICER1-related_tumor_predisposition|Malignant_tumor_of_breast": 1,
    "Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pleuropulmonary_blastoma|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Pleuropulmonary_blastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdomyosarcoma|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_tumor_predisposition|not_provided": 1,
    "not_specified|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|DICER1-related_tumor_predisposition|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided": 1,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_provided": 2,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|DICER1-related_disorder|not_provided": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|Euthyroid_goiter|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|not_specified|not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Euthyroid_goiter|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Pleuropulmonary_blastoma|DICER1-related_disorder": 1,
    "Pleuropulmonary_blastoma|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|DICER1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_disorder|DICER1-related_tumor_predisposition|not_specified": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|DICER1-related_disorder": 1,
    "DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|DICER1-related_tumor_predisposition|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|DICER1-related_tumor_predisposition|not_provided|Pleuropulmonary_blastoma|Euthyroid_goiter|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Rhabdomyosarcoma|_embryonal|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified": 1,
    "Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|not_specified|not_provided": 1,
    "DICER1-related_disorder|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Pleuropulmonary_blastoma|DICER1-related_tumor_predisposition|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Euthyroid_goiter|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Euthyroid_goiter|Rhabdomyosarcoma|_embryonal|_2|Pleuropulmonary_blastoma|DICER1-related_disorder": 1,
    "not_provided|DICER1-related_tumor_predisposition|DICER1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Pleuropulmonary_blastoma|Euthyroid_goiter|DICER1-related_tumor_predisposition": 1,
    "DICER1-related_tumor_predisposition|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|DICER1-related_tumor_predisposition|Breast_neoplasm|not_specified|not_provided|Pleuropulmonary_blastoma": 1,
    "not_provided|DICER1-related_tumor_predisposition|Hereditary_cancer-predisposing_syndrome|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome": 1,
    "Euthyroid_goiter|Pleuropulmonary_blastoma|Rhabdomyosarcoma|_embryonal|_2|Global_developmental_delay_-_lung_cysts_-_overgrowth_-_Wilms_tumor_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|CLMN-related_disorder": 3,
    "CLMN-related_disorder": 13,
    "CLMN-related_disorder|not_provided": 4,
    "not_provided|GLRX5-related_disorder": 2,
    "Spasticity-ataxia-gait_anomalies_syndrome": 3,
    "Spasticity-ataxia-gait_anomalies_syndrome|not_provided": 2,
    "Sideroblastic_anemia_3": 6,
    "not_provided|Sideroblastic_anemia_3": 1,
    "not_specified|not_provided|ATG2B-related_disorder": 2,
    "ATG2B-related_disorder": 19,
    "ATG2B-related_disorder|not_provided": 3,
    "not_provided|ATG2B-related_disorder|not_specified": 2,
    "not_specified|ATG2B-related_disorder": 3,
    "not_provided|not_specified|ATG2B-related_disorder": 1,
    "GSKIP-related_disorder": 1,
    "Spermatogenic_failure_27": 3,
    "not_provided|AK7-related_disorder": 3,
    "AK7-related_disorder|not_provided": 6,
    "Spermatogenic_failure_27|not_provided": 1,
    "AK7-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_1A": 384,
    "VRK1-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_1A|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10": 13,
    "not_specified|Pontocerebellar_hypoplasia_type_1A": 5,
    "Congenital_pontocerebellar_hypoplasia_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1A|Congenital_pontocerebellar_hypoplasia_type_1": 1,
    "not_provided|not_specified|Isolated_microphthalmia_2|Pontocerebellar_hypoplasia_type_1A": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1A": 12,
    "Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases": 13,
    "Congenital_pontocerebellar_hypoplasia_type_1|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases": 2,
    "Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases|not_provided": 2,
    "Pontocerebellar_hypoplasia_type_1A|not_specified|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_1A|not_provided": 4,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10": 3,
    "Pontocerebellar_hypoplasia_type_1A|Pontoneocerebellar_hypoplasia": 2,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10|not_provided|Pontocerebellar_hypoplasia_type_1A": 1,
    "Pontocerebellar_hypoplasia_type_1A|not_specified|not_provided": 2,
    "Congenital_pontocerebellar_hypoplasia_type_1|Pontocerebellar_hypoplasia_type_1A": 2,
    "not_provided|Pontocerebellar_hypoplasia_type_1A|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10": 2,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1A|not_provided": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_1A|Congenital_pontocerebellar_hypoplasia_type_1": 1,
    "Congenital_pontocerebellar_hypoplasia_type_1": 7,
    "not_provided|Pontocerebellar_hypoplasia_type_1A": 8,
    "not_provided|Pontocerebellar_hypoplasia_type_1A|Congenital_pontocerebellar_hypoplasia_type_1": 1,
    "VRK1-related_disorder|not_specified|Pontocerebellar_hypoplasia_type_1A|Congenital_pontocerebellar_hypoplasia_type_1": 1,
    "Distal_spinal_muscular_atrophy|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases": 1,
    "Distal_spinal_muscular_atrophy|not_provided|Pontocerebellar_hypoplasia_type_1A": 1,
    "Pontocerebellar_hypoplasia_type_1A|EMG:_neuropathic_changes|Microcephaly-complex_motor_and_sensory_axonal_neuropathy_syndrome": 1,
    "Distal_spinal_muscular_atrophy|Distal_hereditary_motor_neuropathy_associated_with_upper_motor_neuron_signs|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10": 2,
    "not_specified|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_1A|Congenital_pontocerebellar_hypoplasia_type_1": 3,
    "Congenital_pontocerebellar_hypoplasia_type_1|Pontocerebellar_hypoplasia_type_1A|Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_pontocerebellar_hypoplasia_type_1|not_specified|not_provided|Pontocerebellar_hypoplasia_type_1A": 1,
    "Pontocerebellar_hypoplasia_type_1A|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10|Inborn_genetic_diseases|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_1A|not_specified": 3,
    "not_provided|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases": 1,
    "VRK1-related_disorder|Amyotrophic_lateral_sclerosis|Spinal_muscular_atrophy|Pontocerebellar_hypoplasia_type_1A|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive|Inborn_genetic_diseases|Congenital_pontocerebellar_hypoplasia_type_1|Distal_spinal_muscular_atrophy|not_specified|not_provided": 1,
    "Congenital_pontocerebellar_hypoplasia_type_1|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases|Congenital_pontocerebellar_hypoplasia_type_1": 2,
    "VRK1-related_disorder|not_provided|Pontocerebellar_hypoplasia_type_1A": 1,
    "Juvenile_amyotrophic_lateral_sclerosis|Pontocerebellar_hypoplasia_type_1A|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Pontocerebellar_hypoplasia_type_1A": 1,
    "Inborn_genetic_diseases|not_provided|Pontocerebellar_hypoplasia_type_1A|not_specified": 1,
    "Pontocerebellar_hypoplasia_type_1A|not_provided|Congenital_pontocerebellar_hypoplasia_type_1": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10|Pontocerebellar_hypoplasia_type_1A|Inborn_genetic_diseases|Abnormality_of_the_musculature|Congenital_pontocerebellar_hypoplasia_type_1|not_provided": 1,
    "not_specified|not_provided|Congenital_pontocerebellar_hypoplasia_type_1|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1A": 1,
    "not_provided|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1A": 1,
    "Pontocerebellar_hypoplasia_type_1A|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10|not_provided": 1,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_10|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_1A": 1,
    "Pontocerebellar_hypoplasia_type_1A|Congenital_pontocerebellar_hypoplasia_type_1|Inborn_genetic_diseases": 1,
    "BCL11B-related_disorder": 10,
    "Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 35,
    "BCL11B-related_disorder|not_provided|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 1,
    "not_provided|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 4,
    "Immunodeficiency_49": 5,
    "Immunodeficiency_49|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 3,
    "Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities|not_provided": 3,
    "Immunodeficiency_49|not_provided|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 1,
    "See_cases|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities|not_provided": 1,
    "BCL11B-related_disorder|not_provided": 11,
    "not_provided|BCL11B-related_disorder": 10,
    "not_provided|Immunodeficiency_49|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities": 1,
    "BCL11B-related_disorder|not_specified": 1,
    "not_provided|Immunodeficiency_49": 3,
    "Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities|Immunodeficiency_49|not_provided|BCL11B-related_disorder|not_specified": 1,
    "Combined_immunodeficiency|Immunodeficiency_49": 1,
    "Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities|Immunodeficiency_49": 1,
    "Immunodeficiency_49|not_provided": 1,
    "Intellectual_developmental_disorder_with_speech_delay|_dysmorphic_facies|_and_t-cell_abnormalities|Immunodeficiency_49|not_provided": 1,
    "not_specified|BCL11B-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|BCL11B-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_with_hypertelorism_and_distinctive_facies": 6,
    "CCNK-related_disorder|not_provided": 1,
    "CCNK-related_disorder|Intellectual_developmental_disorder_with_hypertelorism_and_distinctive_facies|not_provided": 1,
    "CCNK-related_disorder": 6,
    "not_specified|Intellectual_developmental_disorder_with_hypertelorism_and_distinctive_facies": 1,
    "EML1-related_disorder": 6,
    "Band_heterotopia_of_brain": 10,
    "Band_heterotopia_of_brain|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|EML1-related_disorder": 1,
    "EML1-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|EML1-related_disorder": 1,
    "not_provided|Band_heterotopia_of_brain": 1,
    "not_provided|EML1-related_disorder": 5,
    "EML1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "EML1-related_disorder|not_specified|not_provided": 1,
    "Gabriele_de_Vries_syndrome": 38,
    "not_provided|YY1-related_disorder": 3,
    "Gabriele_de_Vries_syndrome|not_provided": 1,
    "Gabriele_de_Vries_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Gabriele_de_Vries_syndrome|not_specified|not_provided": 1,
    "YY1-related_disorder": 6,
    "Gabriele_de_Vries_syndrome|Inborn_genetic_diseases": 1,
    "Gabriele_de_Vries_syndrome|not_provided|Intellectual_disability": 2,
    "YY1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Gabriele_de_Vries_syndrome": 1,
    "WARS1-related_disorder|not_provided": 3,
    "Neurodevelopmental_disorder_with_microcephaly_and_speech_delay|_with_or_without_brain_abnormalities": 5,
    "Neuronopathy|_distal_hereditary_motor|_type_9|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_type_9": 6,
    "WARS1-related_disorder|not_provided|Neuronopathy|_distal_hereditary_motor|_type_9": 1,
    "WARS1-related_disorder": 2,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_type_9|WARS1-related_disorder": 1,
    "See_cases|Neuronopathy|_distal_hereditary_motor|_type_9": 1,
    "not_specified|Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_type_9": 1,
    "not_provided|WARS1-related_disorder": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_microcephaly_and_speech_delay|_with_or_without_brain_abnormalities": 1,
    "WARS1-related_disorder|not_specified|not_provided": 1,
    "Central_precocious_puberty": 2,
    "not_provided|DLK1-related_disorder": 1,
    "DLK1-related_disorder": 5,
    "Silver-Russell_syndrome_1|not_provided": 1,
    "DLK1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|DLK1-related_disorder": 1,
    "Paternal_uniparental_disomy_of_chromosome_14": 1,
    "MEG3-related_disorder": 35,
    "MEG3-related_disorder|not_provided": 1,
    "PPP2R5C-related_disorder": 3,
    "Intellectual_disability|HOUGE-JANSSENS_SYNDROME_4|not_specified|not_provided": 1,
    "PPP2R5C-related_disorder|not_provided": 4,
    "not_provided|PPP2R5C-related_disorder": 1,
    "Macrocephaly-developmental_delay_syndrome|not_provided": 8,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 27,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|not_provided": 7,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O": 2850,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 85,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 158,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 84,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|DYNC1H1-related_disorder": 3,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 21,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 173,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_provided": 17,
    "Distal_spinal_muscular_atrophy|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 20,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|DYNC1H1-related_disorder|not_specified|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 20,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 5,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 1,
    "DYNC1H1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 4,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 50,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 59,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease": 12,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13": 10,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 9,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 22,
    "Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|DYNC1H1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 16,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 18,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 2,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Distal_lower_limb_amyotrophy|Pes_cavus|Hammertoe|Myopathy|Dyneinopathy|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Peripheral_neuropathy": 1,
    "DYNC1H1-related_neurological_disorders|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Neurodevelopmental_delay": 1,
    "not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 6,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder": 23,
    "Distal_lower_limb_muscle_weakness|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 2,
    "DYNC1H1-related_disorder": 39,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|DYNC1H1-related_disorder": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 9,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Lissencephaly|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease": 2,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Charcot-Marie-Tooth_disease|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 18,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|See_cases|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O": 12,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Inborn_genetic_diseases": 13,
    "Intellectual_disability|_autosomal_dominant_13|not_provided": 4,
    "Intellectual_disability|_autosomal_dominant_13|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_13": 4,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 3,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|not_specified|DYNC1H1-related_disorder|not_provided": 1,
    "Lissencephaly|Intellectual_disability|_autosomal_dominant_13": 2,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Abnormality_of_neuronal_migration": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 9,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_neurodevelopmental_disorders": 1,
    "Hereditary_motor_and_sensory_neuropathy|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_provided|Inborn_genetic_diseases": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Global_developmental_delay|Polymicrogyria|Motor_delay|Hypotonia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Spinal_muscular_atrophy_with_lower_extremity_predominance": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O": 4,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "not_provided|Spinal_muscular_atrophy_with_lower_extremity_predominance|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Autosomal_dominant_cerebellar_ataxia": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Distal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_neuronopathy": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|not_specified": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|See_cases": 1,
    "DYNC1H1-related_neurodevelopmental_disorders": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "DYNC1H1-related_disorder|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 2,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 4,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "DYNC1H1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease": 1,
    "Polyneuropathy|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Intellectual_disability|_autosomal_dominant_13|Intellectual_disability": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|DYNC1H1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Neurodevelopmental_disorder": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified|Autosomal_dominant_cerebellar_ataxia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_neuronopathy|not_provided": 1,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Intellectual_disability|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|Neurodevelopmental_abnormality": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Charcot-Marie-Tooth_disease|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_neurodevelopmental_disorders": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Hereditary_motor_neuron_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "DYNC1H1-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Spinal_muscular_atrophy_with_lower_extremity_predominance": 1,
    "DYNC1H1-related_disorder|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_13|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease": 2,
    "Lower_limb_muscle_weakness": 2,
    "not_provided|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Inborn_genetic_diseases": 1,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia": 1,
    "not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Spinal_muscular_atrophy_with_lower_extremity_predominance": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Distal_spinal_muscular_atrophy": 1,
    "Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|DYNC1H1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Intellectual_disability|_autosomal_dominant_13": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|not_provided": 2,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_cerebellar_ataxia|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Asphyxiating_thoracic_dystrophy_3": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|not_specified": 2,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 4,
    "not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 4,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|not_provided|Charcot-Marie-Tooth_disease|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 6,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|DYNC1H1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Progressive_muscle_weakness": 1,
    "Inborn_genetic_diseases|DYNC1H1-related_disorder|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 2,
    "Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases|not_provided|Intellectual_disability|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Lissencephaly": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Intellectual_disability|_autosomal_dominant_13|not_provided|Lissencephaly|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|not_provided|DYNC1H1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 2,
    "Asphyxiating_thoracic_dystrophy_3|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|DYNC1H1-related_disorder|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_provided": 3,
    "DYNC1H1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_specified|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|Muscle_weakness|Myopathy|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 5,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Intellectual_Disability|_Dominant|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|not_provided": 1,
    "not_provided|DYNC1H1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder": 1,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|not_provided|DYNC1H1-related_neurodevelopmental_disorders": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_specified": 6,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13": 2,
    "Autosomal_dominant_cerebellar_ataxia|DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|not_provided": 1,
    "DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Asphyxiating_thoracic_dystrophy_3|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Epilepsy_with_generalized_tonic-clonic_seizures": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13": 1,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Microcephaly|Delayed_gross_motor_development|Delayed_speech_and_language_development|Global_developmental_delay|Seizure|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_specified|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "not_provided|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|Intellectual_disability|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "DYNC1H1-related_neurodevelopmental_disorders|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "not_specified|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|DYNC1H1-related_disorder": 2,
    "DYNC1H1-related_disorder|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Autosomal_dominant_cerebellar_ataxia|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Microcephaly|Congenital_cerebellar_hypoplasia|Periventricular_cysts|Small_for_gestational_age|Abnormal_cortical_gyration|Delayed_puberty|Hypoglycemic_encephalopathy|Partial_agenesis_of_the_corpus_callosum|High_palate": 1,
    "Intellectual_disability|_autosomal_dominant_13|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease_type_5|Distal_spinal_muscular_atrophy": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Asphyxiating_thoracic_dystrophy_3|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Rhizomelic_chondrodysplasia_punctata_type_5|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 3,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|not_specified|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Distal_myopathy|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "See_cases|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|DYNC1H1-related_disorder": 1,
    "Inborn_genetic_diseases|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Autosomal_dominant_cerebellar_ataxia|not_provided|Charcot-Marie-Tooth_disease": 1,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|not_specified": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Inborn_genetic_diseases|DYNC1H1-related_disorder": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Autosomal_dominant_cerebellar_ataxia": 3,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder|not_provided": 1,
    "Macrogyria|Global_developmental_delay|Hypoplasia_of_the_corpus_callosum|Microcephaly|Infantile_spasms": 1,
    "DYNC1H1-related_disorder|Intellectual_disability|_autosomal_dominant_13": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Intellectual_disability|_autosomal_dominant_13": 3,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Seizure|Lissencephaly": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Lissencephaly|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_dominant_cerebellar_ataxia|DYNC1H1-related_disorder|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_13|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Lissencephaly": 1,
    "Charcot-Marie-Tooth_disease_type_2|Intellectual_Disability|_Dominant|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|not_provided": 1,
    "Spinal_muscular_atrophy_with_lower_extremity_predominance|Lissencephaly|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 2,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_specified": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|DYNC1H1-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Lissencephaly|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia|not_specified": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|Spinal_muscular_atrophy_with_lower_extremity_predominance": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|not_provided|DYNC1H1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Lissencephaly": 1,
    "DYNC1H1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|not_provided|not_specified": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 2,
    "Charcot-Marie-Tooth_disease|Autosomal_dominant_cerebellar_ataxia|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Inborn_genetic_diseases|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Intellectual_disability|_autosomal_dominant_13|Autism_spectrum_disorder|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|not_specified|DYNC1H1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|not_specified|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Autism_spectrum_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|DYNC1H1-related_disorder": 1,
    "Corpus_callosum|_agenesis_of|Ectopic_tissue|Focal-onset_seizure|Seizure": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|Autism_spectrum_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "Cerebellar_ataxia|Gait_ataxia|Impaired_vibration_sensation_in_the_lower_limbs|Vertigo|Muscle_spasm|Cerebellar_atrophy|Headache": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_dominant_13|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease": 1,
    "not_specified|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|DYNC1H1-related_disorder|Autosomal_dominant_cerebellar_ataxia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified|Charcot-Marie-Tooth_disease|DYNC1H1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13|Autosomal_dominant_cerebellar_ataxia": 1,
    "Autosomal_dominant_cerebellar_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Intellectual_disability|_autosomal_dominant_13": 1,
    "not_provided|DYNC1H1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2O|Autosomal_dominant_cerebellar_ataxia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2O|Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_13": 1,
    "Autosomal_dominant_childhood-onset_proximal_spinal_muscular_atrophy_without_contractures|Charcot-Marie-Tooth_disease_axonal_type_2O|Intellectual_disability|_autosomal_dominant_13|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Dolichocephaly|Delayed_speech_and_language_development": 1,
    "Intellectual_disability|Seizure|Microcephaly": 1,
    "Hereditary_spastic_paraplegia_49|not_provided": 20,
    "Hereditary_spastic_paraplegia_49|not_provided|Hereditary_spastic_paraplegia|not_specified": 1,
    "Hereditary_spastic_paraplegia_49": 1108,
    "Hereditary_spastic_paraplegia_49|TECPR2-related_disorder": 5,
    "TECPR2-related_disorder|Hereditary_spastic_paraplegia_49": 5,
    "not_provided|Hereditary_spastic_paraplegia_49": 30,
    "Intellectual_disability|_FRA12A_type|Hereditary_spastic_paraplegia_49|Inborn_genetic_diseases": 1,
    "TECPR2-related_disorder": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_49": 14,
    "not_specified|Hereditary_spastic_paraplegia_49": 10,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 12,
    "Hereditary_spastic_paraplegia_49|not_specified": 6,
    "not_specified|Hereditary_spastic_paraplegia_49|not_provided|Hereditary_spastic_paraplegia": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_49": 2,
    "TECPR2-related_disorder|Hereditary_spastic_paraplegia_49|not_provided": 1,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia_49|not_specified": 1,
    "Hereditary_spastic_paraplegia|TECPR2-related_disorder": 1,
    "not_provided|Hereditary_spastic_paraplegia|TECPR2-related_disorder|Hereditary_spastic_paraplegia_49": 1,
    "Hereditary_spastic_paraplegia_49|Inborn_genetic_diseases": 20,
    "Hereditary_spastic_paraplegia_49|not_specified|not_provided": 2,
    "TECPR2-related_disorder|Hereditary_spastic_paraplegia_49|not_specified": 1,
    "Hereditary_spastic_paraplegia_49|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_49": 3,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_49": 2,
    "not_provided|TECPR2-related_disorder|not_specified|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_49|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|not_provided": 3,
    "TECPR2-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_49": 1,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_49": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 1,
    "TECPR2-related_disorder|not_provided|Hereditary_spastic_paraplegia_49": 2,
    "not_provided|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_49|Inborn_genetic_diseases": 1,
    "TECPR2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_49": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_49|not_provided": 2,
    "Hereditary_spastic_paraplegia_49|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Hereditary_spastic_paraplegia_49|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|not_specified": 2,
    "Hereditary_spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia_49": 1,
    "Hereditary_spastic_paraplegia_49|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_spastic_paraplegia_49|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia|not_provided|See_cases|Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_49": 1,
    "Hereditary_spastic_paraplegia_49|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_49|TECPR2-related_disorder|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_49|not_provided": 1,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|TECPR2-related_disorder|not_provided|not_specified|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "not_provided|Hereditary_spastic_paraplegia_49|not_specified|Inherited_spastic_paresis|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_49|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_49|TECPR2-related_disorder": 1,
    "not_specified|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 1,
    "Sensory_autonomic_neuropathy_with_intellectual_disability|Hereditary_spastic_paraplegia_49": 1,
    "not_provided|TECPR2-related_disorder|Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia": 1,
    "not_specified|TECPR2-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_49": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_49|not_provided": 1,
    "Hereditary_spastic_paraplegia_49|Hereditary_spastic_paraplegia|TECPR2-related_disorder|not_provided": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3": 328,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3|TRAF3-related_disorder": 5,
    "not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_3": 12,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3|not_specified": 6,
    "TRAF3-related_disorder|not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_3": 1,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_3": 7,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3|not_specified|not_provided": 2,
    "Immunodeficiency_132b": 2,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3|not_provided|TRAF3-related_disorder": 2,
    "not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_3|TRAF3-related_disorder": 1,
    "TRAF3-related_disorder": 1,
    "Immunodeficiency_132b|Herpes_simplex_encephalitis|_susceptibility_to|_3": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3|not_provided": 2,
    "TRAF3-related_disorder|Herpes_simplex_encephalitis|_susceptibility_to|_3": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_3|Multisystem_inflammatory_syndrome_in_children": 1,
    "TRAF3_haploinsufficiency": 1,
    "Imerslund-Grasbeck_syndrome_type_2": 59,
    "Imerslund-Grasbeck_syndrome_type_2|Inborn_genetic_diseases": 6,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2": 14,
    "Imerslund-Grasbeck_syndrome_type_2|Imerslund-Grasbeck_syndrome": 36,
    "Imerslund-Grasbeck_syndrome_type_2|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases": 3,
    "AMN-related_disorder|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2": 1,
    "Imerslund-Grasbeck_syndrome_type_2|not_provided": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2|not_provided": 1,
    "Imerslund-Grasbeck_syndrome_type_2|Cobalamin_deficiency|Megaloblastic_anemia": 1,
    "AMN-related_disorder|Imerslund-Grasbeck_syndrome|not_provided": 1,
    "Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_2": 1,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2|not_provided": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_1|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2": 1,
    "Cobalamin_deficiency|Megaloblastic_anemia": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_2|Imerslund-Grasbeck_syndrome": 4,
    "Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2|Inborn_genetic_diseases": 2,
    "Imerslund-Grasbeck_syndrome_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_2|Imerslund-Grasbeck_syndrome": 5,
    "not_provided|Imerslund-Grasbeck_syndrome|Imerslund-Grasbeck_syndrome_type_2|AMN-related_disorder": 1,
    "Imerslund-Grasbeck_syndrome_type_2|Imerslund-Grasbeck_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Imerslund-Grasbeck_syndrome_type_2|Imerslund-Grasbeck_syndrome|not_provided": 1,
    "Imerslund-Grasbeck_syndrome|AMN-related_disorder": 1,
    "not_provided|Imerslund-Grasbeck_syndrome_type_2": 2,
    "Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_2": 1,
    "Imerslund-Grasbeck_syndrome|not_specified": 1,
    "AMN-related_disorder|Imerslund-Grasbeck_syndrome": 2,
    "AMN-related_disorder": 1,
    "not_provided|Imerslund-Grasbeck_syndrome|Inborn_genetic_diseases|Imerslund-Grasbeck_syndrome_type_1": 1,
    "CDC42BPB-related_disorder": 31,
    "Chilton-Okur-Chung_neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "Chilton-Okur-Chung_neurodevelopmental_syndrome": 35,
    "CDC42BPB-related_disorder|not_provided": 7,
    "not_provided|CDC42BPB-related_disorder": 4,
    "CDC42BPB-related_neurodevelopmental_syndrome": 5,
    "CDC42BPB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CDC42BPB-related_neurodevelopmental_syndrome": 2,
    "Chilton-Okur-Chung_neurodevelopmental_syndrome|CDC42BPB-related_neurodevelopmental_syndrome": 3,
    "CDC42BPB-related_disorder|Chilton-Okur-Chung_neurodevelopmental_syndrome|not_provided|CDC42BPB-related_neurodevelopmental_syndrome": 1,
    "Inborn_genetic_diseases|CDC42BPB-related_disorder": 1,
    "not_provided|Chilton-Okur-Chung_neurodevelopmental_syndrome": 1,
    "Autism_spectrum_disorder|Chilton-Okur-Chung_neurodevelopmental_syndrome|CDC42BPB-related_neurodevelopmental_syndrome": 1,
    "CDC42BPB-related_Neurodevelopmental_disorder": 1,
    "MARK3-related_disorder": 11,
    "not_provided|MARK3-related_disorder|Visual_impairment_and_progressive_phthisis_bulbi": 1,
    "Visual_impairment_and_progressive_phthisis_bulbi": 1,
    "Cardiomyopathy|_dilated|_2F": 5,
    "not_provided|COA8-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_17|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "COA8-related_disorder": 5,
    "not_provided|COA8-related_disorder|not_specified": 1,
    "not_specified|COA8-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_specified|not_provided": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_17": 4,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|COA8-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17": 10,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_provided": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_provided": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_17|COA8-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_specified": 1,
    "COA8-related_disorder|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_17": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_17": 1,
    "COA8-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_specified|not_provided|COA8-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_17|not_provided|not_specified": 1,
    "XRCC3-related_disorder": 5,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_6|XRCC3-related_disorder|not_provided": 1,
    "not_provided|Spermatogenic_failure_30": 1,
    "TDRD9-related_disorder": 18,
    "not_specified|TDRD9-related_disorder|not_provided": 1,
    "Spermatogenic_failure_30|not_specified": 1,
    "Spermatogenic_failure_30|Azoospermia": 1,
    "Spermatogenic_failure_30": 5,
    "not_provided|TDRD9-related_disorder": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_11": 11,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_11|not_specified": 2,
    "not_specified|Cortical_dysplasia|_complex|_with_other_brain_malformations_11": 2,
    "Focal_segmental_glomerulosclerosis_5": 43,
    "not_provided|Focal_segmental_glomerulosclerosis_5": 5,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|Focal_segmental_glomerulosclerosis_5": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 694,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 42,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|INF2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|not_provided": 2,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 314,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 12,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases": 21,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 2,
    "not_provided|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 2,
    "INF2-related_disorder|Proteinuria": 1,
    "Charcot-Marie-Tooth_disease|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 3,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 31,
    "Periodic_fever_syndrome": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 21,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided": 15,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Charcot-Marie-Tooth_disease": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|INF2-related_disorder": 6,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E": 8,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 8,
    "INF2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 6,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 19,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided|Inborn_genetic_diseases": 5,
    "not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 2,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|not_specified": 4,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 2,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|INF2-related_disorder": 1,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases": 2,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Focal_segmental_glomerulosclerosis_5|INF2-related_disorder": 1,
    "INF2-related_disorder|not_specified|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 10,
    "Focal_segmental_glomerulosclerosis_5|Focal_segmental_glomerulosclerosis": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified": 7,
    "Kidney_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "not_specified|INF2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Charcot-Marie-Tooth_disease": 1,
    "Kidney_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Kidney_disorder|Focal_segmental_glomerulosclerosis_5": 1,
    "Charcot-Marie-Tooth_disease|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Renal_insufficiency|Focal_segmental_glomerulosclerosis|Proteinuria|Hypertensive_disorder|not_provided": 1,
    "Inborn_genetic_diseases|INF2-related_disorder": 1,
    "INF2-related_disorder": 9,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified": 9,
    "not_provided|INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "not_provided|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 6,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided|Kidney_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 9,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 4,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|not_provided": 2,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|not_provided|INF2-related_disorder": 1,
    "Inborn_genetic_diseases|INF2-related_disorder|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|INF2-related_disorder|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 3,
    "not_provided|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 3,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_5|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified": 1,
    "Focal_segmental_glomerulosclerosis|not_provided|not_specified": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified": 5,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|INF2-related_disorder|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|not_provided": 2,
    "INF2-related_disorder|not_specified|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "not_provided|INF2-related_disorder": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 6,
    "Focal_segmental_glomerulosclerosis_5|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided|INF2-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified|not_provided": 4,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified|Inborn_genetic_diseases|not_provided|Kidney_disorder": 1,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|Kidney_disorder": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|INF2-related_disorder": 1,
    "not_specified|INF2-related_disorder|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "not_provided|not_specified|INF2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|INF2-related_disorder": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|INF2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|Inborn_genetic_diseases": 2,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|INF2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Kidney_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 2,
    "Focal_segmental_glomerulosclerosis|INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Kidney_disorder|not_provided": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 2,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|INF2-related_disorder|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 1,
    "Glomerulonephritis|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|INF2-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|not_provided": 4,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_5|not_specified": 1,
    "not_provided|Kidney_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified": 2,
    "Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|not_provided": 3,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|Corticosteroids_response": 1,
    "INF2-related_disorder|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_specified|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 2,
    "not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|INF2-related_disorder": 1,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 2,
    "Kidney_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|INF2-related_disorder|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|INF2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_5|not_provided|INF2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Kidney_disorder|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|INF2-related_disorder": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|not_specified|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|Nephrotic_syndrome": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5|not_provided|Focal_segmental_glomerulosclerosis|INF2-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|Kidney_disorder": 1,
    "INF2-related_disorder|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided|not_specified": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_5|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5|not_provided|Chronic_kidney_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Motor_polyneuropathy|Interosseus_muscle_atrophy|Mixed_demyelinating_and_axonal_polyneuropathy|Progressive_pes_cavus|Premature_birth|Oligohydramnios|Small_for_gestational_age|Birth_length_less_than_3rd_percentile": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "INF2-related_disorder|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Focal_segmental_glomerulosclerosis_5": 1,
    "not_specified|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|not_provided|Inborn_genetic_diseases|INF2-related_disorder|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|INF2-related_disorder|not_provided|Focal_segmental_glomerulosclerosis_5|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "Focal_segmental_glomerulosclerosis_5|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_E": 1,
    "not_specified|Charcot-Marie-Tooth_disease|not_provided|Focal_segmental_glomerulosclerosis_5": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_5": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_5": 2,
    "Focal_segmental_glomerulosclerosis_5|not_provided|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_5|not_specified|not_provided": 1,
    "Myopathy|_distal|_5": 15,
    "ADSS1-related_disorder": 8,
    "not_provided|ADSS1-related_disorder": 2,
    "not_provided|Myopathy|_distal|_5": 12,
    "Myopathy|_distal|_5|Inborn_genetic_diseases|not_provided": 1,
    "Myopathy|_distal|_5|not_provided": 2,
    "ADSS1-related_disorder|not_provided": 8,
    "ADSS1-related_disorder|not_specified|Myopathy|_distal|_5|not_provided": 1,
    "not_provided|Myopathy|_distal|_5|Inborn_genetic_diseases": 4,
    "Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|Myopathy|_distal|_5|not_provided": 1,
    "Myopathy|_distal|_5|ADSS1-related_disorder|not_provided": 1,
    "ADSS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|ADSS1-related_disorder|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_6": 278,
    "Cowden_syndrome_6|Inborn_genetic_diseases": 71,
    "Cowden_syndrome_6|AKT1-related_disorder|Inborn_genetic_diseases": 2,
    "Proteus_syndrome": 2,
    "Inborn_genetic_diseases|Cowden_syndrome_6": 73,
    "Colorectal_cancer|Proteus_syndrome|Ovarian_cancer|Cowden_syndrome_6|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|Cowden_syndrome_6": 3,
    "not_provided|Cowden_syndrome_6": 6,
    "AKT1-related_disorder|Cowden_syndrome_6": 4,
    "Cowden_syndrome_6|Ovarian_cancer|Familial_cancer_of_breast|Proteus_syndrome|Colorectal_cancer": 1,
    "Cowden_syndrome_6|Familial_cancer_of_breast|Ovarian_cancer|Proteus_syndrome|Colorectal_cancer|AKT1-related_disorder": 1,
    "not_specified|Cowden_syndrome_6|not_provided|Inborn_genetic_diseases|AKT1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Cowden_syndrome_6": 4,
    "not_provided|Inborn_genetic_diseases|Cowden_syndrome_6": 2,
    "not_specified|Cowden_syndrome_6|AKT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Cowden_syndrome_6|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_6|not_provided|Inborn_genetic_diseases": 2,
    "AKT1-related_disorder|Cowden_syndrome_6|not_provided|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_6|AKT1-related_disorder": 3,
    "not_provided|AKT1-related_disorder|Inborn_genetic_diseases|Cowden_syndrome_6": 1,
    "Familial_cancer_of_breast|Proteus_syndrome|Colorectal_cancer|Ovarian_cancer|Cowden_syndrome_6|Inborn_genetic_diseases": 1,
    "Proteus_syndrome|Cowden_syndrome_6|Familial_cancer_of_breast|Ovarian_neoplasm|Colorectal_cancer|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Cowden_syndrome_6": 1,
    "Cowden_syndrome_6|Familial_cancer_of_breast|Ovarian_cancer|Colorectal_cancer|Proteus_syndrome": 1,
    "Cowden_syndrome_6|Inborn_genetic_diseases|not_provided": 2,
    "AKT1-related_disorder|Inborn_genetic_diseases|Cowden_syndrome_6": 1,
    "not_specified|Cowden_syndrome_6|not_provided": 1,
    "Inborn_genetic_diseases|Cowden_syndrome_6|not_provided": 1,
    "Cowden_syndrome_6|not_provided": 4,
    "Schizophrenia|Cowden_syndrome_6": 1,
    "not_specified|not_provided|Cowden_syndrome_6": 1,
    "Cowden_syndrome_6|not_provided|not_specified": 2,
    "not_provided|not_specified|Cowden_syndrome_6": 1,
    "Cowden_syndrome_6|Familial_cancer_of_breast|Proteus_syndrome|Colorectal_cancer|Ovarian_cancer": 1,
    "Familial_cancer_of_breast|Proteus_syndrome|Colorectal_cancer|Ovarian_cancer|Cowden_syndrome_6": 1,
    "Familial_cancer_of_breast|Proteus_syndrome|Colorectal_cancer|Ovarian_cancer|Cowden_syndrome_6|not_provided|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_6|Familial_cancer_of_breast|Proteus_syndrome|Colorectal_cancer|Ovarian_cancer|AKT1-related_disorder|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_6|not_specified|Inborn_genetic_diseases": 1,
    "Cowden_syndrome_6|Inborn_genetic_diseases|AKT1-related_disorder": 1,
    "Familial_cancer_of_breast|Cowden_syndrome_6|Ovarian_cancer|Proteus_syndrome|Colorectal_cancer": 1,
    "Cowden_syndrome_6|not_specified": 1,
    "Familial_cancer_of_breast|Colorectal_cancer|Cowden_syndrome_6|Proteus_syndrome|Ovarian_cancer": 1,
    "Proteus_syndrome|Familial_cancer_of_breast|Ovarian_cancer|Cowden_syndrome_6|Colorectal_cancer|not_provided": 1,
    "AKT1-related_disorder|Hereditary_cancer|not_specified|not_provided|Cowden_syndrome_6": 1,
    "Familial_cancer_of_breast|Proteus_syndrome|Ovarian_cancer|Cowden_syndrome_6|Colorectal_cancer": 1,
    "not_provided|Cowden_syndrome_6|Ovarian_neoplasm|Proteus_syndrome|Carcinoma_of_colon|Breast_adenocarcinoma": 1,
    "not_provided|Lethal_congenital_contracture_syndrome_6": 1,
    "ZBTB42-related_disorder": 2,
    "ZBTB42-related_disorder|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_6|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_6|not_specified": 1,
    "Lethal_congenital_contracture_syndrome_6": 1,
    "not_provided|CEP170B-related_disorder": 4,
    "CEP170B-related_disorder": 60,
    "Heart|_malformation_of|not_provided": 1,
    "not_specified|CEP170B-related_disorder": 2,
    "CEP170B-related_disorder|not_specified": 1,
    "not_specified|Enhancement_of_the_C-reflex": 1,
    "Migraine|Hereditary_episodic_ataxia": 1,
    "Dysmetria|not_provided": 1,
    "not_provided|AHNAK2-related_disorder": 3,
    "AHNAK2-related_disorder": 2,
    "AHNAK2-related_disorder|not_provided": 1,
    "JAG2-related_disorder": 38,
    "JAG2-related_disorder|not_provided": 10,
    "not_specified|not_provided|JAG2-related_disorder": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_27": 25,
    "not_provided|JAG2-related_disorder": 10,
    "JAG2-related_disorder|not_specified|not_provided": 1,
    "JAG2-related_disorder|not_specified": 1,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_recessive_27": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_recessive_27|not_provided": 1,
    "Cerebellar-facial-dental_syndrome": 7,
    "BRF1-related_disorder": 7,
    "Inborn_genetic_diseases|not_provided|Cerebellar-facial-dental_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Cerebellar-facial-dental_syndrome": 1,
    "not_provided|BRF1-related_disorder": 1,
    "Inborn_genetic_diseases|Dystonia|_early-onset|_and/or_spastic_paraplegia": 2,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|BRF1-related_disorder": 1,
    "Inborn_genetic_diseases|Cerebellar-facial-dental_syndrome": 2,
    "BRF1-related_disorder|not_provided": 2,
    "Cerebellar-facial-dental_syndrome|not_provided": 2,
    "Cerebellar-facial-dental_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Cerebellar-facial-dental_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Heart|_malformation_of|Sensorineural_hearing_loss_disorder|Primary_microcephaly|Postnatal_growth_retardation|Intellectual_disability|_moderate|Abnormality_of_the_inner_ear": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_66": 4,
    "not_provided|PACS2-related_disorder": 15,
    "Developmental_and_epileptic_encephalopathy|_66|not_provided": 12,
    "Developmental_and_epileptic_encephalopathy|_66": 19,
    "PACS2-related_disorder|not_provided": 18,
    "PACS2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_66": 1,
    "not_provided|PACS2-related_disorder|Developmental_and_epileptic_encephalopathy|_66": 1,
    "Developmental_and_epileptic_encephalopathy|_66|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|PACS2-related_disorder|See_cases|Inborn_genetic_diseases|not_provided|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_66|Inborn_genetic_diseases|not_provided": 1,
    "PACS2-related_disorder": 5,
    "PACS2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_66|See_cases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_66|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_66|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|PACS2-related_disorder": 1,
    "Decreased_circulating_IgG2_concentration": 1,
    "Autosomal_recessive_agammaglobulinemia_1": 20,
    "Autosomal_recessive_agammaglobulinemia_1|not_provided": 1,
    "NIPA1-related_disorder": 2,
    "Hereditary_spastic_paraplegia_6": 213,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_6": 2,
    "not_specified|Hereditary_spastic_paraplegia_6": 3,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_6|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_6": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_6|not_specified": 1,
    "Spastic_paraplegia|_autosomal_dominant|Hereditary_spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia_6": 1,
    "not_specified|Hereditary_spastic_paraplegia_6|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_6|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|_autosomal_dominant|Hereditary_spastic_paraplegia_6|not_specified|not_provided": 1,
    "not_provided|not_specified|NIPA1-related_disorder|Hereditary_spastic_paraplegia_6": 1,
    "Hereditary_spastic_paraplegia_6|not_provided": 14,
    "not_provided|Hereditary_spastic_paraplegia_6": 15,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_6": 1,
    "Hereditary_spastic_paraplegia_6|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_6|Hereditary_spastic_paraplegia|NIPA1-related_disorder|not_specified|not_provided": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_6": 1,
    "not_provided|NIPA1-related_disorder": 2,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_6|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia|NIPA1-related_disorder|Hereditary_spastic_paraplegia_6": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_6": 3,
    "Hereditary_spastic_paraplegia_6|not_specified": 2,
    "Hereditary_spastic_paraplegia_6|NIPA1-related_disorder": 1,
    "not_provided|Hereditary_spastic_paraplegia_6|Spastic_paraplegia|_autosomal_dominant": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_6|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_6|NIPA1-related_disorder": 1,
    "NIPA1-related_disorder|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_6|Hereditary_spastic_paraplegia": 1,
    "NIPA2-related_disorder": 7,
    "not_provided|NIPA2-related_disorder": 2,
    "CYFIP1-related_disorder": 3,
    "Autism|Strabismus|Atrial_septal_defect|Delayed_speech_and_language_development|Cognitive_impairment|Autistic_behavior|not_specified": 1,
    "Autism|Strabismus|Atrial_septal_defect|Delayed_speech_and_language_development|Cognitive_impairment|Autistic_behavior": 1,
    "Precocious_puberty|_central|_2": 9,
    "MKRN3-related_disorder": 4,
    "Prader-Willi_syndrome": 14,
    "Precocious_puberty|_central|_2|Prader-Willi_syndrome": 2,
    "MKRN3-related_disorder|not_provided": 1,
    "Precocious_puberty|_central|_2|not_provided|MKRN3-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|MKRN3-related_disorder": 1,
    "not_provided|MKRN3-related_disorder": 1,
    "not_provided|MAGEL2-related_disorder": 37,
    "not_provided|Schaaf-Yang_syndrome": 10,
    "MAGEL2-related_disorder": 84,
    "MAGEL2-related_disorder|Inborn_genetic_diseases|not_provided": 15,
    "MAGEL2-related_disorder|not_provided": 42,
    "Schaaf-Yang_syndrome|MAGEL2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MAGEL2-related_disorder": 9,
    "MAGEL2-related_disorder|Schaaf-Yang_syndrome|not_provided": 3,
    "Schaaf-Yang_syndrome|not_provided": 16,
    "Inborn_genetic_diseases|MAGEL2-related_disorder|not_provided": 7,
    "not_provided|Inborn_genetic_diseases|MAGEL2-related_disorder|Schaaf-Yang_syndrome": 1,
    "not_provided|MAGEL2-related_disorder|Inborn_genetic_diseases": 5,
    "MAGEL2-related_disorder|not_specified|not_provided": 3,
    "Prader-Willi_syndrome|Prader-Willi-like_syndrome|not_provided": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Intellectual_disability|not_specified|not_provided": 1,
    "Prader-Willi_syndrome|Schaaf-Yang_syndrome|not_provided|not_specified": 1,
    "MAGEL2-related_disorder|not_provided|Inborn_genetic_diseases": 9,
    "not_specified|MAGEL2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|MAGEL2-related_disorder": 10,
    "not_specified|Inborn_genetic_diseases|MAGEL2-related_disorder|not_provided": 1,
    "MAGEL2-related_disorder|Inborn_genetic_diseases": 7,
    "Schaaf-Yang_syndrome|not_provided|MAGEL2-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|MAGEL2-related_disorder": 7,
    "MAGEL2-related_disorder|not_provided|not_specified": 1,
    "MAGEL2-related_disorder|Schaaf-Yang_syndrome": 4,
    "Inborn_genetic_diseases|Schaaf-Yang_syndrome|not_provided": 5,
    "Schaaf-Yang_syndrome|Prader-Willi_syndrome|not_provided": 1,
    "not_provided|MAGEL2-related_disorder|Schaaf-Yang_syndrome": 2,
    "not_provided|Schaaf-Yang_syndrome|MAGEL2-related_disorder": 2,
    "MAGEL2-related_disorder|Schaaf-Yang_syndrome|Prader-Willi_syndrome": 1,
    "not_provided|not_specified|Schaaf-Yang_syndrome|Inborn_genetic_diseases": 1,
    "Schaaf-Yang_syndrome|MAGEL2-related_disorder": 2,
    "not_provided|Prader-Willi_syndrome|Schaaf-Yang_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Prader-Willi-like_syndrome|Schaaf-Yang_syndrome|Neurodevelopmental_disorder|not_provided|Neurodevelopmental_delay|See_cases": 1,
    "Ambiguous_genitalia|Generalized_hypotonia|Ventriculomegaly|Multiple_joint_contractures|Schaaf-Yang_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Prader-Willi_syndrome|Schaaf-Yang_syndrome": 1,
    "Schaaf-Yang_syndrome|Prader-Willi_syndrome": 3,
    "Intellectual_disability|Schaaf-Yang_syndrome": 1,
    "Schaaf-Yang_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Schaaf-Yang_syndrome|Prader-Willi_syndrome|not_provided|MAGEL2-related_disorder": 1,
    "MAGEL2-related_disorder|Inborn_genetic_diseases|Prader-Willi_syndrome|Schaaf-Yang_syndrome|not_provided": 1,
    "Intellectual_disability|not_provided|MAGEL2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Schaaf-Yang_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|MAGEL2-related_disorder|Schaaf-Yang_syndrome": 1,
    "Prader-Willi_syndrome|Schaaf-Yang_syndrome|not_provided": 1,
    "Schaaf-Yang_syndrome|Prader-Willi_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Schaaf-Yang_syndrome": 1,
    "MAGEL2-related_disorder|not_provided|Schaaf-Yang_syndrome|Inborn_genetic_diseases": 1,
    "Schaaf-Yang_syndrome|not_provided|MAGEL2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Schaaf-Yang_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Schaaf-Yang_syndrome|MAGEL2-related_disorder": 1,
    "Prader-Willi_syndrome|not_provided|MAGEL2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Prader-Willi_syndrome|Schaaf-Yang_syndrome|not_provided|not_specified": 1,
    "not_provided|Prader-Willi_syndrome|Schaaf-Yang_syndrome": 1,
    "not_specified|not_provided|Prader-Willi_syndrome": 1,
    "MAGEL2-related_disorder|Inborn_genetic_diseases|Schaaf-Yang_syndrome": 1,
    "Inborn_genetic_diseases|Prader-Willi_syndrome|not_specified|not_provided": 1,
    "Developmental_disorder|Schaaf-Yang_syndrome": 1,
    "NDN-related_disorder": 2,
    "Prader-Willi_syndrome|not_provided": 3,
    "not_provided|Autism_spectrum_disorder|Thalidomide_response": 1,
    "SNRPN-related_condition": 1,
    "Angelman_syndrome|Autism|not_specified|Autism_spectrum_disorder": 1,
    "Angelman_syndrome": 520,
    "not_provided|Angelman_syndrome": 54,
    "Angelman_syndrome|not_provided": 42,
    "Inborn_genetic_diseases|UBE3A-related_disorder|not_specified|not_provided|Angelman_syndrome": 1,
    "not_specified|not_provided|Angelman_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Angelman_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Angelman_syndrome": 6,
    "Angelman_syndrome|See_cases|not_provided": 1,
    "Neurodevelopmental_disorder|Angelman_syndrome|Inborn_genetic_diseases": 1,
    "UBE3A-related_disorder": 11,
    "Angelman_syndrome|Inborn_genetic_diseases": 11,
    "not_specified|Angelman_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Angelman_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Angelman_syndrome|UBE3A-related_disorder": 1,
    "Angelman_syndrome|not_specified": 5,
    "not_specified|Angelman_syndrome": 17,
    "Global_developmental_delay|Poor_speech|EEG_abnormality|Abnormal_corpus_callosum_morphology|Expressive_language_delay|Seizure": 1,
    "Angelman_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Angelman_syndrome": 10,
    "Angelman_syndrome|Inborn_genetic_diseases|not_specified": 2,
    "UBE3A-related_disorder|not_specified|not_provided|Angelman_syndrome": 2,
    "UBE3A-related_disorder|Angelman_syndrome": 2,
    "not_provided|Angelman_syndrome|Inborn_genetic_diseases": 2,
    "UBE3A-related_disorder|not_provided|Angelman_syndrome": 2,
    "Inborn_genetic_diseases|UBE3A-related_disorder|Angelman_syndrome": 1,
    "not_provided|not_specified|Angelman_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Angelman_syndrome": 4,
    "not_provided|Inborn_genetic_diseases|Angelman_syndrome": 5,
    "Angelman_syndrome|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Angelman_syndrome|not_provided": 3,
    "not_provided|Angelman_syndrome|UBE3A-related_disorder": 1,
    "not_provided|Epileptic_encephalopathy|Angelman_syndrome": 1,
    "Autism|Inborn_genetic_diseases": 4,
    "Angelman_syndrome|UBE3A-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Angelman_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Angelman_syndrome|not_provided": 1,
    "not_specified|Angelman_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|See_cases|Angelman_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_myopathy|not_provided|Angelman_syndrome": 1,
    "Angelman_syndrome|not_provided|not_specified": 1,
    "UBE3A-related_disorder|not_specified|Angelman_syndrome": 1,
    "Intellectual_disability|Angelman_syndrome": 1,
    "Angelman_syndrome|Inborn_genetic_diseases|UBE3A-related_disorder|not_provided": 1,
    "not_provided|Angelman_syndrome|not_specified": 1,
    "UBE3A-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Angelman_syndrome": 1,
    "Angelman_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Angelman_syndrome": 1,
    "Angelman_syndrome|not_specified|not_provided": 1,
    "ATP10A-related_disorder": 28,
    "ATP10A-related_disorder|not_provided": 10,
    "not_provided|ATP10A-related_disorder": 2,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 155,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 18,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 195,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|not_provided": 15,
    "Developmental_and_epileptic_encephalopathy|_43": 34,
    "GABRB3-related_disorder|Seizure|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 16,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided|GABRB3-related_disorder|Developmental_and_epileptic_encephalopathy|_43": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_43|not_provided|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "GABRB3-related_disorder|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 1,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 7,
    "not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|Inborn_genetic_diseases|Intellectual_disability|not_provided": 1,
    "GABRB3-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|not_specified|not_provided|Seizure": 1,
    "GABRB3-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|not_specified": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 9,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|Developmental_and_epileptic_encephalopathy|_43": 3,
    "GABRB3-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 2,
    "not_provided|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43": 1,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Inborn_genetic_diseases": 5,
    "Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 2,
    "Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_5": 2,
    "not_specified|Seizure|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_specified": 9,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43|not_provided": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|Inborn_genetic_diseases": 4,
    "Developmental_and_epileptic_encephalopathy|_43|not_provided": 2,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided|Developmental_and_epileptic_encephalopathy|_43": 1,
    "Neurodevelopmental_delay|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_43": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5": 4,
    "Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 2,
    "Global_developmental_delay|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "not_specified|GABRB3-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "not_provided|Seizure|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 2,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epileptic_encephalopathy": 2,
    "not_specified|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|GABRB3-related_disorder": 1,
    "Intellectual_disability|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Intellectual_disability": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|not_specified|not_provided": 1,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|GABRB3-related_disorder": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43": 4,
    "Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|Insomnia|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|GABRB3-related_disorder|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Seizure": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided|GABRB3-related_disorder": 2,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|GABRB3-related_disorder": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "GABRB3-related_disorder": 5,
    "Epilepsy|Neurodevelopmental_delay|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Inborn_genetic_diseases|not_provided": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|not_provided|not_specified": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43": 1,
    "not_provided|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|not_specified": 1,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5": 1,
    "not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_5|Epilepsy|_childhood_absence|_susceptibility_to|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "GABRB3-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_5|Developmental_and_epileptic_encephalopathy|_43|Epilepsy|_childhood_absence|_susceptibility_to|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_1|Epilepsy|_childhood_absence|_susceptibility_to|_5|not_provided": 1,
    "GABRA5-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_79": 16,
    "Developmental_and_epileptic_encephalopathy|_79|not_provided": 6,
    "not_provided|Focal_epilepsy|Developmental_and_epileptic_encephalopathy|_79": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_79": 2,
    "Developmental_and_epileptic_encephalopathy|_79|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|GABRA5-related_disorder|Inborn_genetic_diseases": 1,
    "GABRG3-related_disorder": 2,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided": 15,
    "Tyrosinase-positive_oculocutaneous_albinism|not_specified|not_provided": 8,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism": 33,
    "not_provided|Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism": 18,
    "Tyrosinase-positive_oculocutaneous_albinism|not_provided": 20,
    "OCA2-related_disorder": 7,
    "OCA2-related_disorder|not_provided|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 2,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Oculocutaneous_albinism": 3,
    "Nonsyndromic_Oculocutaneous_Albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided|OCA2-related_disorder": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 2,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Oculocutaneous_albinism|Albinism|Inborn_genetic_diseases|OCA2-related_disorder": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 7,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism": 10,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "Oculocutaneous_albinism|not_provided|Inborn_genetic_diseases": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|OCA2-related_disorder": 1,
    "OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided": 6,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_specified|not_provided": 2,
    "OCA2-related_disorder|not_provided": 10,
    "not_provided|OCA2-related_disorder": 8,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Oculocutaneous_albinism|Nonsyndromic_Oculocutaneous_Albinism|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 1,
    "OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Oculocutaneous_albinism|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|OCA2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 7,
    "not_provided|not_specified|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|OCA2-related_disorder": 3,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "OCA2-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided": 1,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 6,
    "OCA2-related_disorder|Oculocutaneous_albinism|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Oculocutaneous_albinism|not_provided": 2,
    "not_specified|OCA2-related_disorder|not_provided": 1,
    "Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 3,
    "Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Oculocutaneous_albinism|Motor_delay|_mild|Respiratory_tract_infection|Diarrhea|Congenital_nystagmus|Inborn_genetic_diseases|not_specified|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Nonsyndromic_Oculocutaneous_Albinism|not_provided": 1,
    "not_provided|Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "OCA2-related_disorder|not_specified|Inborn_genetic_diseases|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|not_provided|not_specified": 3,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|Oculocutaneous_albinism|not_provided": 1,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder": 1,
    "not_provided|Cone-rod_dystrophy|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 3,
    "not_provided|Albinism|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided|OCA2-related_disorder": 2,
    "OCA2-related_disorder|Oculocutaneous_albinism|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided": 1,
    "not_provided|Nonsyndromic_Oculocutaneous_Albinism|Oculocutaneous_albinism|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "OCA2-related_disorder|not_specified|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 2,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Oculocutaneous_albinism|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Albinism_or_congenital_nystagmus|OCA2-related_disorder|Inborn_genetic_diseases|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided|See_cases": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Oculocutaneous_albinism": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|OCA2-related_disorder|Inborn_genetic_diseases|Oculocutaneous_albinism|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 2,
    "not_provided|OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 3,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_specified|not_provided": 1,
    "OCA2-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 1,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Oculocutaneous_albinism|not_specified": 1,
    "Albinism_or_congenital_nystagmus|Nonsyndromic_Oculocutaneous_Albinism|OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Oculocutaneous_albinism|not_provided": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|not_provided|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 2,
    "not_specified|Tyrosinase-positive_oculocutaneous_albinism|not_provided": 2,
    "not_provided|OCA2-related_disorder|not_specified|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Inborn_genetic_diseases|Albinism_or_congenital_nystagmus|Oculocutaneous_albinism|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided|Oculocutaneous_albinism": 1,
    "Nonsyndromic_Oculocutaneous_Albinism|not_specified|not_provided": 1,
    "OCA2-related_disorder|Inborn_genetic_diseases|not_provided|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_specified|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "not_provided|Nonsyndromic_Oculocutaneous_Albinism|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Inborn_genetic_diseases": 1,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism|not_specified": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Oculocutaneous_albinism|Albinism|OCA2-related_disorder": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_provided|not_specified": 1,
    "not_provided|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Tyrosinase-positive_oculocutaneous_albinism|not_specified|OCA2-related_disorder": 1,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|OCA2-related_disorder": 1,
    "Albinism": 2,
    "Brown_oculocutaneous_albinism|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder|not_provided": 1,
    "OCA2-related_disorder|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Inborn_genetic_diseases": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Oculocutaneous_albinism|not_provided": 1,
    "not_specified|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 2,
    "not_specified|not_provided|Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder": 1,
    "not_provided|not_specified|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Oculocutaneous_albinism": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Oculocutaneous_albinism|not_provided|Hypophosphatasia": 1,
    "Oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|OCA2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|OCA2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder|not_provided": 1,
    "not_provided|Tyrosinase-positive_oculocutaneous_albinism|OCA2-related_disorder|not_specified": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|not_provided": 1,
    "not_provided|HERC2-related_disorder": 13,
    "HERC2-related_disorder": 38,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|not_provided": 11,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 51,
    "Inborn_genetic_diseases|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "Prader-Willi_syndrome|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 12,
    "HERC2-related_disorder|not_provided": 14,
    "not_provided|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 6,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 1,
    "Global_developmental_delay|not_provided|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 1,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|not_provided": 1,
    "HERC2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES": 1,
    "Inborn_genetic_diseases|HERC2-related_disorder|not_specified": 1,
    "HERC2-related_disorder|concomitant_exotropia|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|HERC2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Inborn_genetic_diseases": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Prader-Willi_syndrome|not_provided": 1,
    "HERC2-related_disorder|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Prader-Willi_syndrome": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 2,
    "Optic_nerve_hypoplasia|Intellectual_disability|_severe|Aplasia/Hypoplasia_of_the_cerebellum|Neonatal_hypotonia|Global_brain_atrophy|Hypoplasia_of_the_corpus_callosum|Paraparesis|Motor_delay": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 2,
    "Inborn_genetic_diseases|HERC2-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Prader-Willi_syndrome|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 1,
    "Inborn_genetic_diseases|Prader-Willi_syndrome": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 1,
    "Prader-Willi_syndrome|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 1,
    "Prader-Willi_syndrome|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|not_provided": 1,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|not_provided|HERC2-related_disorder|SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Prader-Willi_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability": 1,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|not_specified|not_provided": 1,
    "Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Inborn_genetic_diseases": 2,
    "HERC2-related_disorder|not_specified|not_provided": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_1|_BLUE/NONBLUE_EYES|Developmental_delay_with_autism_spectrum_disorder_and_gait_instability|Inborn_genetic_diseases": 1,
    "not_provided|HERC2-related_disorder|Inborn_genetic_diseases": 1,
    "APBA2-related_disorder|not_provided": 6,
    "APBA2-related_disorder": 18,
    "not_provided|APBA2-related_disorder": 11,
    "APBA2-related_disorder|not_specified|not_provided": 1,
    "Lung_disease|_immunodeficiency|_and_chromosome_breakage_syndrome%3B|not_provided": 4,
    "Lung_disease|_immunodeficiency|_and_chromosome_breakage_syndrome%3B|Lung_damage|_immunodeficiency_and_chromosome_breakage_syndrome|not_provided": 1,
    "Lung_damage|_immunodeficiency_and_chromosome_breakage_syndrome|Lung_disease|_immunodeficiency|_and_chromosome_breakage_syndrome%3B": 1,
    "not_provided|NSMCE3-related_disorder": 3,
    "NSMCE3-related_disorder|not_provided": 1,
    "not_specified|NSMCE3-related_disorder": 1,
    "NSMCE3-related_disorder|not_provided|not_specified": 1,
    "TJP1-related_disorder": 28,
    "not_provided|TJP1-related_disorder": 4,
    "not_specified|not_provided|TJP1-related_disorder": 1,
    "not_specified|TJP1-related_disorder": 1,
    "not_provided|Karyomegalic_interstitial_nephritis": 21,
    "Karyomegalic_interstitial_nephritis": 134,
    "FAN1-related_disorder|not_provided": 12,
    "Inborn_genetic_diseases|Karyomegalic_interstitial_nephritis": 5,
    "Karyomegalic_interstitial_nephritis|not_provided": 13,
    "not_provided|FAN1-related_disorder|Karyomegalic_interstitial_nephritis": 2,
    "Karyomegalic_interstitial_nephritis|not_provided|Inborn_genetic_diseases": 1,
    "Karyomegalic_interstitial_nephritis|FAN1-related_disorder|not_provided": 3,
    "Karyomegalic_interstitial_nephritis|FAN1-related_disorder": 5,
    "not_provided|Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome|FAN1-related_disorder": 1,
    "Karyomegalic_interstitial_nephritis|Inborn_genetic_diseases": 9,
    "not_provided|FAN1-related_disorder": 8,
    "FAN1-related_disorder": 16,
    "FAN1-related_disorder|Karyomegalic_interstitial_nephritis": 2,
    "Karyomegalic_interstitial_nephritis|not_provided|not_specified": 3,
    "not_specified|Karyomegalic_interstitial_nephritis|not_provided|FAN1-related_disorder": 1,
    "Karyomegalic_interstitial_nephritis|FAN1-related_disorder|Inborn_genetic_diseases": 1,
    "Karyomegalic_interstitial_nephritis|Inborn_genetic_diseases|FAN1-related_disorder": 1,
    "Inborn_genetic_diseases|FAN1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Karyomegalic_interstitial_nephritis": 2,
    "Inborn_genetic_diseases|not_provided|Karyomegalic_interstitial_nephritis": 1,
    "Karyomegalic_interstitial_nephritis|Kidney_failure|not_provided": 1,
    "FAN1-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|FAN1-related_disorder|Karyomegalic_interstitial_nephritis": 1,
    "Karyomegalic_interstitial_nephritis|Inborn_genetic_diseases|not_provided": 1,
    "FAN1-related_disorder|not_provided|Karyomegalic_interstitial_nephritis": 1,
    "Congenital_stationary_night_blindness_1C|not_provided": 53,
    "Inborn_genetic_diseases|not_provided|Congenital_stationary_night_blindness_1C": 2,
    "TRPM1-related_disorder|Congenital_stationary_night_blindness_1C|not_provided": 3,
    "TRPM1-related_disorder|not_provided": 11,
    "Congenital_stationary_night_blindness_1C|Retinal_dystrophy|not_provided|Optic_atrophy": 1,
    "not_provided|Congenital_stationary_night_blindness_1C": 27,
    "not_provided|TRPM1-related_disorder|Congenital_stationary_night_blindness_1C": 4,
    "Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_1C": 1,
    "Hereditary_macular_dystrophy|not_provided": 1,
    "not_specified|not_provided|TRPM1-related_disorder": 1,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1C": 6,
    "not_provided|TRPM1-related_disorder": 7,
    "Congenital_stationary_night_blindness_1C|not_provided|not_specified": 2,
    "not_provided|Congenital_stationary_night_blindness_1C|Cone-rod_dystrophy|TRPM1-related_disorder": 1,
    "not_specified|not_provided|TRPM1-related_disorder|Congenital_stationary_night_blindness_1C": 1,
    "not_provided|Congenital_stationary_night_blindness_1C|Inborn_genetic_diseases": 1,
    "TRPM1-related_disorder": 11,
    "Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_1C|Inborn_genetic_diseases": 1,
    "Congenital_stationary_night_blindness_1C|TRPM1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|TRPM1-related_disorder": 1,
    "not_provided|Congenital_stationary_night_blindness_1C|Congenital_stationary_night_blindness": 1,
    "Congenital_stationary_night_blindness_1C|TRPM1-related_disorder|Congenital_stationary_night_blindness": 1,
    "not_provided|Congenital_stationary_night_blindness_1C|not_specified": 1,
    "Congenital_stationary_night_blindness_1C|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_1C|not_provided": 2,
    "Retinal_dystrophy|Congenital_stationary_night_blindness_1C": 1,
    "Congenital_stationary_night_blindness_1C|Intellectual_disability": 1,
    "not_provided|Hereditary_macular_dystrophy|TRPM1-related_disorder": 1,
    "Congenital_stationary_night_blindness_1C|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Congenital_stationary_night_blindness_1C": 2,
    "TRPM1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Night_blindness|Congenital_stationary_night_blindness_1C|Congenital_stationary_night_blindness": 1,
    "Congenital_stationary_night_blindness_1C|not_specified|not_provided": 1,
    "TRPM1-related_disorder|Inborn_genetic_diseases|not_provided|Congenital_stationary_night_blindness_1C": 1,
    "TRPM1-related_disorder|not_provided|Congenital_stationary_night_blindness_1C": 3,
    "Retinal_dystrophy|not_specified|not_provided|Congenital_stationary_night_blindness_1C": 1,
    "TRPM1-related_disorder|not_provided|Retinitis_pigmentosa|Congenital_stationary_night_blindness_1C": 1,
    "not_provided|Retinal_dystrophy|Congenital_stationary_night_blindness_1C": 1,
    "not_specified|TRPM1-related_disorder|not_provided": 1,
    "OTUD7A-related_disorder": 15,
    "not_provided|OTUD7A-related_disorder": 2,
    "OTUD7A-related_disorder|not_provided": 2,
    "OTUD7A-related_disorder|not_specified": 2,
    "Neurodevelopmental_disorder_with_hypotonia_and_seizures": 1,
    "Language_disorder|Epileptic_encephalopathy|Severe_global_developmental_delay|Specific_learning_disability|Neurodevelopmental_disorder_with_hypotonia_and_seizures": 1,
    "not_specified|OTUD7A-related_disorder": 1,
    "not_provided|CHRNA7-related_disorder": 2,
    "CHRNA7-related_disorder": 1,
    "CHRNA7-related_disorder|not_provided": 1,
    "Chromosome_15q13.3_microdeletion_syndrome": 1,
    "Hereditary_mixed_polyposis_syndrome|not_provided": 1,
    "Polyposis_syndrome|_hereditary_mixed|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "GREM1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "GREM1-related_disorder|Polyposis_syndrome|_hereditary_mixed|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_mixed_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer|not_provided": 1,
    "GREM1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|GREM1-related_disorder": 3,
    "Hereditary_mixed_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_mixed_polyposis_syndrome": 1,
    "GREM1-related_disorder": 2,
    "GREM1-related_disorder|Hereditary_mixed_polyposis_syndrome": 1,
    "not_specified|FMN1-related_disorder": 1,
    "FMN1-related_disorder": 11,
    "not_specified|not_provided|FMN1-related_disorder": 3,
    "not_provided|FMN1-related_disorder|not_specified": 1,
    "not_provided|FMN1-related_disorder": 10,
    "FMN1-related_disorder|not_specified|not_provided": 2,
    "not_provided|not_specified|FMN1-related_disorder": 1,
    "FMN1-related_disorder|not_provided": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 640,
    "Epileptic_encephalopathy|not_specified|Congenital_myopathy_20": 1,
    "RYR3-related_disorder|Epileptic_encephalopathy": 8,
    "Epileptic_encephalopathy|Congenital_myopathy_20": 2,
    "Epileptic_encephalopathy|not_specified": 191,
    "RYR3-related_disorder": 13,
    "RYR3-related_Epileptic_encephalopathy|not_specified": 3,
    "Epileptic_encephalopathy|RYR3-related_Epileptic_encephalopathy": 1,
    "RYR3-related_disorder|not_provided|Epileptic_encephalopathy": 6,
    "Epileptic_encephalopathy|RYR3-related_disorder": 17,
    "not_provided|Epileptic_encephalopathy|RYR3-related_disorder": 3,
    "not_provided|RYR3-related_disorder": 1,
    "Congenital_myopathy_20|Flexion_contracture": 1,
    "Congenital_myopathy_20": 8,
    "Epileptic_encephalopathy|Flexion_contracture|not_provided": 1,
    "not_provided|Epileptic_encephalopathy|RYR3-related_disorder|not_specified": 1,
    "Premature_ovarian_failure|Epileptic_encephalopathy|See_cases": 1,
    "RYR3-related_disorder|Epileptic_encephalopathy|not_provided|not_specified": 1,
    "Epileptic_encephalopathy|not_provided|Monomelic_amyotrophy": 1,
    "RYR3-related_Epileptic_encephalopathy|not_specified|not_provided": 1,
    "RYR3-related_disorder|Epileptic_encephalopathy|not_provided": 5,
    "not_specified|RYR3-related_Epileptic_encephalopathy|Epileptic_encephalopathy": 1,
    "Congenital_myopathy_20|Epileptic_encephalopathy": 4,
    "Epileptic_encephalopathy|Congenital_myopathy_20|not_provided": 1,
    "Congenital_myopathy_20|not_provided|Epileptic_encephalopathy": 1,
    "RYR3-related_Epileptic_encephalopathy": 3,
    "Epileptic_encephalopathy|RYR3-related_disorder|not_provided": 4,
    "not_provided|RYR3-related_disorder|Epileptic_encephalopathy": 4,
    "RYR3-related_disorder|not_provided": 1,
    "RYR3-related_Epileptic_encephalopathy|Epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|not_specified|not_provided": 3,
    "Epileptic_encephalopathy|not_specified|not_provided|RYR3-related_disorder": 1,
    "Epileptic_encephalopathy|Flexion_contracture|Congenital_myopathy_20": 2,
    "RYR3-related_disorder|not_specified|Epileptic_encephalopathy": 1,
    "not_specified|RYR3-related_disorder|Epileptic_encephalopathy": 1,
    "not_provided|not_specified|Epileptic_encephalopathy": 3,
    "not_provided|Inborn_genetic_diseases|not_specified|Epileptic_encephalopathy": 1,
    "Congenital_myopathy_20|not_specified": 2,
    "Epileptic_encephalopathy|not_provided|not_specified": 2,
    "Epileptic_encephalopathy|See_cases": 1,
    "Epileptic_encephalopathy|RYR3-related_disorder|not_specified": 2,
    "not_specified|RYR3-related_Epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|Arthrogryposis_multiplex_congenita": 1,
    "See_cases|Epileptic_encephalopathy": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 291,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided": 45,
    "Charcot-Marie-Tooth_disease|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 2,
    "SLC12A6-related_disorder|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II": 7,
    "not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 50,
    "not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II": 2,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Inborn_genetic_diseases|not_provided": 3,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 2,
    "not_specified|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 4,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 2,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_specified|not_provided": 6,
    "not_specified|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided": 3,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided|not_specified": 7,
    "not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Inborn_genetic_diseases": 3,
    "SLC12A6-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|SLC12A6-related_disorder|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|SLC12A6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|SLC12A6-related_disorder": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II": 1,
    "SLC12A6-related_disorder|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided": 3,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 1,
    "not_provided|Inborn_genetic_diseases|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 7,
    "not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Inborn_genetic_diseases|SLC12A6-related_disorder": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II": 2,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II": 3,
    "SLC12A6-related_disorder|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 3,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided": 3,
    "Autosomal_recessive_axonal_hereditary_motor_and_sensory_neuropathy": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|not_provided": 3,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|not_provided|Peripheral_neuropathy": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_specified|not_provided|SLC12A6-related_disorder|Inborn_genetic_diseases": 1,
    "SLC12A6-related_disorder|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|SLC12A6-related_disorder": 2,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_specified|SLC12A6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|SLC12A6-related_disorder": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|not_provided": 2,
    "SLC12A6-related_disorder|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Corpus_callosum|_agenesis_of|Low-set_ears|Abnormal_facial_shape|Clinodactyly_of_the_5th_finger|Hypertelorism": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|Inborn_genetic_diseases|not_provided": 1,
    "SLC12A6-related_disorder|not_specified|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Inborn_genetic_diseases": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|SLC12A6-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_provided|not_specified": 1,
    "not_provided|not_specified|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|not_provided": 1,
    "Usher_syndrome_type_1C|not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II": 1,
    "SLC12A6-related_disorder|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_specified|not_provided": 1,
    "not_provided|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Charcot-Marie-Tooth_disease|_axonal|_IIa_2II|not_specified": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|not_specified": 1,
    "SLC12A6-related_disorder": 1,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Dyskeratosis_Congenita|_Recessive|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_1": 47,
    "Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Dyskeratosis_congenita|_autosomal_recessive_1|Dyskeratosis_Congenita|_Recessive|not_provided": 3,
    "Dyskeratosis_congenita|_autosomal_recessive_1|not_specified|not_provided": 2,
    "Dyskeratosis_Congenita|_Recessive|not_provided": 3,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_1|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_1|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_1|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_9|Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_2": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_1|not_specified": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_1|not_specified": 1,
    "Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_2": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_9|not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_1": 1,
    "Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_2|Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_9|Dyskeratosis_congenita|_autosomal_recessive_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Dyskeratosis_congenita|_autosomal_recessive_1": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure_syndrome|_telomere-related|_9": 1,
    "Dyskeratosis_Congenita|_Recessive": 11,
    "not_provided|Dyskeratosis_Congenita|_Recessive|not_specified": 1,
    "Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 24,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 21,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy|Atrial_septal_defect": 7,
    "Dilated_cardiomyopathy_1R|not_provided|Hypertrophic_cardiomyopathy_11": 13,
    "ACTC1-related_disorder|Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy|Atrial_septal_defect": 1,
    "Dilated_cardiomyopathy_1R|ACTC1-related_disorder|Hypertrophic_cardiomyopathy_11": 1,
    "not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 6,
    "not_provided|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 2,
    "Dilated_Cardiomyopathy|_Dominant|Familial_restrictive_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect": 15,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect": 2,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided": 1,
    "Dilated_Cardiomyopathy|_Dominant|Left_ventricular_noncompaction_cardiomyopathy|Familial_restrictive_cardiomyopathy|Atrial_septal_defect|Hypertrophic_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11": 27,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 42,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 31,
    "Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype|not_specified": 1,
    "Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5": 20,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 2,
    "Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Cardiovascular_phenotype": 4,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Cardiomyopathy": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 6,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype": 6,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 106,
    "not_specified|Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|ACTC1-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|not_provided": 4,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11": 3,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 2,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided": 2,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 5,
    "Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|not_provided": 2,
    "Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 14,
    "Hypertrophic_cardiomyopathy_11": 4,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy|Cardiomyopathy": 3,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_provided": 6,
    "Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect|Left_ventricular_noncompaction_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Cardiovascular_phenotype|not_provided|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 1,
    "Hypertrophic_cardiomyopathy_11|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 3,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 5,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype|ACTC1-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Atrial_septal_defect_5|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1R": 4,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Cardiovascular_phenotype": 2,
    "not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Cardiovascular_phenotype": 2,
    "Dilated_cardiomyopathy_1A|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 1,
    "not_specified|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "not_provided|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy|Atrial_septal_defect|Left_ventricular_noncompaction_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|not_specified": 1,
    "Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|not_provided|Atrial_septal_defect|Dilated_Cardiomyopathy|_Dominant|not_specified": 2,
    "not_specified|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified": 3,
    "ACTC1-related_disorder|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "Dilated_cardiomyopathy_1R|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Familial_restrictive_cardiomyopathy|not_provided|ACTC1-related_disorder|not_specified|Atrial_septal_defect": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_specified|not_provided": 1,
    "ACTC1-related_disorder|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified": 1,
    "not_specified|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|ACTC1-related_disorder": 1,
    "ACTC1-related_disorder|Dilated_Cardiomyopathy|_Dominant|Primary_dilated_cardiomyopathy|Familial_restrictive_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Atrial_septal_defect|not_specified": 1,
    "Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|ACTC1-related_disorder|not_provided|not_specified": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified|Hypertrophic_cardiomyopathy_2|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_specified|ACTC1-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiomyopathy": 5,
    "not_provided|Dilated_cardiomyopathy_1R": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 2,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|not_provided": 1,
    "Cardiovascular_phenotype|See_cases|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy": 1,
    "ACTC1-related_disorder": 3,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 3,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided|Cardiovascular_phenotype": 2,
    "Atrial_septal_defect_5": 4,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_provided|Cardiovascular_phenotype|ACTC1-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "not_provided|not_specified|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy_11|ACTC1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiomyopathy": 3,
    "Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_provided": 2,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|ACTC1-related_disorder|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided": 1,
    "Inborn_genetic_diseases|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11": 1,
    "ACTC1-related_disorder|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 1,
    "Cardiovascular_phenotype|ACTC1-related_disorder": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|ACTC1-related_disorder|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 1,
    "Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype": 2,
    "not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11": 1,
    "not_specified|Cardiovascular_phenotype|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy|Cardiomyopathy": 2,
    "ACTC1-related_disorder|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|ACTC1-related_disorder|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 2,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy": 2,
    "not_provided|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy|not_specified|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Cardiomyopathy": 1,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided": 1,
    "Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype": 2,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy|ACTC1-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|ACTC1-related_disorder": 1,
    "Cardiomyopathy|not_provided|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11": 1,
    "Cardiovascular_phenotype|ACTC1-related_disorder|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_specified": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_4|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_11": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1R": 1,
    "Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 1,
    "Dilated_cardiomyopathy_1R|not_provided": 1,
    "not_specified|ACTC1-related_disorder|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified": 1,
    "not_specified|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|not_provided": 1,
    "ACTC1-related_disorder|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|not_specified|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Cardiomyopathy": 1,
    "Left_ventricular_dilatation": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|ACTC1-related_disorder": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_provided": 1,
    "Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11": 1,
    "Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R": 1,
    "not_provided|Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|not_specified": 1,
    "not_specified|Hypertrophic_cardiomyopathy_11|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_septal_defect_5|Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_11|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Cardiovascular_phenotype|not_provided": 2,
    "Dilated_cardiomyopathy_1R|Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1R|Atrial_septal_defect_5|Hypertrophic_cardiomyopathy_11|Cardiovascular_phenotype": 1,
    "Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Atrial_septal_defect|Dilated_Cardiomyopathy|_Dominant|not_specified": 1,
    "Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant|not_provided|Atrial_septal_defect": 1,
    "Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Atrial_septal_defect|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|Atrial_septal_defect": 3,
    "AQR-related_condition": 1,
    "not_provided|Congenital_dyserythropoietic_anemia_type_type_1B": 5,
    "CDIN1-related_disorder|not_provided": 1,
    "Congenital_dyserythropoietic_anemia_type_type_1B": 11,
    "not_provided|not_specified|Congenital_dyserythropoietic_anemia_type_type_1B": 1,
    "not_provided|CDIN1-related_disorder": 1,
    "not_specified|not_provided|Congenital_dyserythropoietic_anemia_type_type_1B": 1,
    "Congenital_dyserythropoietic_anemia_type_type_1B|not_provided": 5,
    "Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies": 84,
    "not_provided|MEIS2-related_disorder": 1,
    "Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies|Inborn_genetic_diseases": 2,
    "MEIS2-related_disorder": 8,
    "Inborn_genetic_diseases|Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies": 2,
    "Cleft_palate|MEIS2-related_disorder|not_provided|Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies|Inborn_genetic_diseases": 1,
    "Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies|not_provided|Inborn_genetic_diseases": 1,
    "Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies|not_provided": 4,
    "MEIS2-related_disorder|Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies": 3,
    "Inborn_genetic_diseases|not_provided|Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies": 1,
    "not_provided|MEIS2-related_disorder|Cardiac_malformation|_cleft_lip/palate|_microcephaly|_and_digital_anomalies": 1,
    "Legius_syndrome": 436,
    "Legius_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Legius_syndrome|Cardiovascular_phenotype": 74,
    "Cardiovascular_phenotype|Legius_syndrome|not_specified": 3,
    "Cardiovascular_phenotype|Legius_syndrome": 66,
    "not_specified|Cardiovascular_phenotype|SPRED1-related_disorder|Legius_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided|SPRED1-related_disorder|not_specified|Legius_syndrome": 1,
    "not_specified|Legius_syndrome": 10,
    "Legius_syndrome|not_specified": 6,
    "not_provided|Legius_syndrome": 27,
    "Cardiovascular_phenotype|not_specified|Legius_syndrome": 7,
    "not_provided|Cardiovascular_phenotype|Legius_syndrome": 4,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome|Legius_syndrome": 2,
    "Legius_syndrome|not_provided": 26,
    "Legius_syndrome|Cardiovascular_phenotype|not_provided": 4,
    "Incidental_Discovery|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Legius_syndrome": 1,
    "Legius_syndrome|Cardiovascular_phenotype|not_specified": 5,
    "Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Legius_syndrome": 3,
    "SPRED1-related_disorder|Legius_syndrome": 1,
    "SPRED1-related_disorder|Cardiovascular_phenotype|Legius_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Legius_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "Legius_syndrome|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 3,
    "not_provided|not_specified|Legius_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Legius_syndrome|Cardiovascular_phenotype|not_specified": 2,
    "not_specified|Legius_syndrome|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|not_provided|Legius_syndrome": 4,
    "Noonan_syndrome_and_Noonan-related_syndrome|Legius_syndrome": 4,
    "Legius_syndrome|not_provided|not_specified": 1,
    "not_provided|Legius_syndrome|not_specified": 2,
    "not_provided|not_specified|Legius_syndrome": 1,
    "Noonan_syndrome|Legius_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Legius_syndrome": 1,
    "Inborn_genetic_diseases|Legius_syndrome": 1,
    "Legius_syndrome|Neurofibromatosis|_type_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|SPRED1-related_disorder|Legius_syndrome": 1,
    "Legius_syndrome|Neurodevelopmental_delay|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Legius_syndrome|Cardiovascular_phenotype|SPRED1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Legius_syndrome": 3,
    "not_provided|Legius_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|SPRED1-related_disorder|Legius_syndrome": 1,
    "Legius_syndrome|See_cases": 1,
    "Legius_syndrome|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Legius_syndrome": 2,
    "Legius_syndrome|Noonan_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Legius_syndrome|Costello_syndrome": 1,
    "Legius_syndrome|not_provided|SPRED1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "Legius_syndrome|not_provided|Cardiovascular_phenotype": 3,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Legius_syndrome": 2,
    "not_specified|not_provided|Legius_syndrome|Cardiovascular_phenotype": 1,
    "SPRED1-related_disorder": 1,
    "SPRED1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Legius_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|SPRED1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Legius_syndrome": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Legius_syndrome|not_provided": 1,
    "SPRED1-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Legius_syndrome": 1,
    "Legius_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|Legius_syndrome|not_provided": 3,
    "not_specified|Legius_syndrome|SPRED1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Legius_syndrome|SPRED1-related_disorder": 1,
    "Cardiovascular_phenotype|Legius_syndrome|Neurofibromatosis-Noonan_syndrome": 1,
    "not_specified|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Legius_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Cardiovascular_phenotype|not_provided|Legius_syndrome": 1,
    "Legius_syndrome|Male_infertility_with_spermatogenesis_disorder|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 1,
    "Noonan_syndrome|Legius_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Legius_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Legius_syndrome|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Legius_syndrome": 1,
    "not_provided|SPRED1-related_disorder|Cardiovascular_phenotype|Legius_syndrome": 1,
    "Cardiovascular_phenotype|Legius_syndrome|Neurofibromatosis|_type_1|not_provided": 1,
    "Legius_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Legius_syndrome|not_provided": 1,
    "Legius_syndrome|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Noonan_syndrome|Legius_syndrome|not_specified": 1,
    "not_provided|RASGRP1-related_disorder": 4,
    "Immunodeficiency_64|not_provided": 3,
    "Immunodeficiency_64": 17,
    "RASGRP1-related_disorder|not_provided": 4,
    "RASGRP1-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency_64": 2,
    "not_specified|not_provided|RASGRP1-related_disorder": 1,
    "not_provided|Immunodeficiency_64": 2,
    "THBS1-related_disorder": 10,
    "THBS1-related_disorder|not_specified|not_provided": 1,
    "not_provided|THBS1-related_disorder|not_specified": 2,
    "not_provided|not_specified|THBS1-related_disorder": 1,
    "not_provided|THBS1-related_disorder": 2,
    "not_specified|THBS1-related_disorder|not_provided": 1,
    "Familial_pulmonary_capillary_hemangiomatosis": 54,
    "EIF2AK4-related_disorder|not_provided": 5,
    "not_specified|Familial_pulmonary_capillary_hemangiomatosis|not_provided": 1,
    "not_provided|Familial_pulmonary_capillary_hemangiomatosis": 10,
    "Familial_pulmonary_capillary_hemangiomatosis|not_provided": 16,
    "EIF2AK4-related_disorder": 9,
    "Inborn_genetic_diseases|Familial_pulmonary_capillary_hemangiomatosis": 2,
    "not_provided|Pulmonary_arterial_hypertension": 1,
    "not_provided|Familial_pulmonary_capillary_hemangiomatosis|not_specified": 4,
    "Inborn_genetic_diseases|EIF2AK4-related_disorder": 1,
    "not_specified|not_provided|Familial_pulmonary_capillary_hemangiomatosis": 3,
    "not_provided|not_specified|Familial_pulmonary_capillary_hemangiomatosis": 2,
    "EIF2AK4-related_disorder|Familial_pulmonary_capillary_hemangiomatosis|not_provided": 1,
    "Familial_pulmonary_capillary_hemangiomatosis|not_specified|not_provided": 3,
    "not_provided|Familial_pulmonary_capillary_hemangiomatosis|Pulmonary_arterial_hypertension": 1,
    "not_provided|Familial_pulmonary_capillary_hemangiomatosis|EIF2AK4-related_disorder": 1,
    "Familial_pulmonary_capillary_hemangiomatosis|Inborn_genetic_diseases|not_provided": 1,
    "Familial_pulmonary_capillary_hemangiomatosis|not_provided|EIF2AK4-related_disorder": 1,
    "Familial_pulmonary_capillary_hemangiomatosis|not_provided|not_specified": 1,
    "not_provided|not_specified|EIF2AK4-related_disorder|Familial_pulmonary_capillary_hemangiomatosis": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 195,
    "Colorectal_cancer|not_specified|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1|not_provided|BUB1B-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1": 177,
    "Mosaic_variegated_aneuploidy_syndrome_1|not_specified|not_provided": 2,
    "Mosaic_variegated_aneuploidy_syndrome_1|Colorectal_cancer|Premature_chromatid_separation_trait": 12,
    "not_specified|Carcinoma_of_colon|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Colorectal_cancer|not_provided": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1": 5,
    "Inborn_genetic_diseases|not_specified|Mosaic_variegated_aneuploidy_syndrome_1": 2,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Colorectal_cancer": 2,
    "Mosaic_variegated_aneuploidy_syndrome|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Colorectal_cancer": 1,
    "Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Colorectal_cancer|Premature_chromatid_separation_trait|not_specified|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Colorectal_cancer|Inborn_genetic_diseases|not_provided|not_specified|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait": 1,
    "BUB1B-related_disorder": 3,
    "Mosaic_variegated_aneuploidy_syndrome_1|not_specified": 2,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "See_cases|Premature_chromatid_separation_trait|Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait": 1,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_1|Colorectal_cancer|Premature_chromatid_separation_trait": 1,
    "Premature_chromatid_separation_trait": 3,
    "Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Colorectal_cancer|Inborn_genetic_diseases": 2,
    "not_provided|Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 1,
    "Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1": 6,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_1": 5,
    "Mosaic_variegated_aneuploidy_syndrome_1|BUB1B-related_disorder": 1,
    "not_specified|not_provided|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Mosaic_variegated_aneuploidy_syndrome|Inborn_genetic_diseases": 1,
    "Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Carcinoma_of_colon": 2,
    "not_provided|Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait": 1,
    "not_specified|Mosaic_variegated_aneuploidy_syndrome_1": 4,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1|BUB1B-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Carcinoma_of_colon|not_specified|not_provided": 1,
    "Premature_chromatid_separation_trait|Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Ovarian_cancer": 1,
    "Ovarian_cancer|Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Mosaic_variegated_aneuploidy_syndrome|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Carcinoma_of_colon|not_specified|not_provided": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait": 3,
    "Ovarian_cancer|Inborn_genetic_diseases": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Colorectal_cancer|Premature_chromatid_separation_trait|not_provided|Inborn_genetic_diseases": 1,
    "BUB1B-related_disorder|Premature_chromatid_separation_trait|Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1": 2,
    "Premature_chromatid_separation_trait|Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|not_specified|not_provided": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|not_provided|Premature_chromatid_separation_trait|Colorectal_cancer": 1,
    "not_provided|BUB1B-related_disorder|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Inborn_genetic_diseases|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Carcinoma_of_colon|Colorectal_cancer": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|See_cases|BUB1B-related_disorder|Inborn_genetic_diseases|Colorectal_cancer": 1,
    "Inborn_genetic_diseases|Mosaic_variegated_aneuploidy_syndrome_1|not_provided|Colorectal_cancer": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|not_provided": 3,
    "Mosaic_variegated_aneuploidy_syndrome_1|not_specified|Premature_chromatid_separation_trait|Colorectal_cancer|Inborn_genetic_diseases": 1,
    "Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Carcinoma_of_colon|not_provided|not_specified|Colorectal_cancer": 1,
    "Inborn_genetic_diseases|Carcinoma_of_colon|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|not_provided": 1,
    "not_provided|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 1,
    "Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Inborn_genetic_diseases": 1,
    "Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|not_provided|not_specified": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|Colorectal_cancer": 4,
    "Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ovarian_cancer|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "not_provided|Colorectal_cancer|not_specified|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1": 2,
    "Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Colorectal_cancer|not_specified|not_provided": 1,
    "Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 2,
    "not_specified|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases": 1,
    "Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Colorectal_cancer": 1,
    "BUB1B-related_disorder|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|See_cases": 1,
    "Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|not_provided|Inborn_genetic_diseases|Microcephaly": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|not_provided|Colorectal_cancer|Premature_chromatid_separation_trait|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait": 1,
    "not_provided|Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|not_specified": 1,
    "not_provided|Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1|not_specified|Inborn_genetic_diseases": 1,
    "Colorectal_cancer|Premature_chromatid_separation_trait|Mosaic_variegated_aneuploidy_syndrome_1": 1,
    "Mosaic_variegated_aneuploidy_syndrome_1|Premature_chromatid_separation_trait|not_specified|Colorectal_cancer": 1,
    "BUB1B-related_disorder|Mosaic_variegated_aneuploidy_syndrome_1|not_provided": 1,
    "Colorectal_cancer|Mosaic_variegated_aneuploidy_syndrome_1|not_provided|Premature_chromatid_separation_trait|not_specified": 1,
    "Isovaleryl-CoA_dehydrogenase_deficiency": 581,
    "not_provided|Isovaleryl-CoA_dehydrogenase_deficiency": 31,
    "not_provided|not_specified|Isovaleryl-CoA_dehydrogenase_deficiency": 1,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_specified|IVD-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Isovaleryl-CoA_dehydrogenase_deficiency": 8,
    "Isovaleryl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 7,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_provided|not_specified": 2,
    "IVD-related_disorder|Isovaleryl-CoA_dehydrogenase_deficiency": 3,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_specified": 8,
    "not_specified|not_provided|Isovaleryl-CoA_dehydrogenase_deficiency": 5,
    "Isovaleric_acidemia|_type_I": 1,
    "Inborn_genetic_diseases|Isovaleryl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "IVD-related_disorder|not_provided|Isovaleryl-CoA_dehydrogenase_deficiency": 2,
    "not_specified|Isovaleryl-CoA_dehydrogenase_deficiency": 16,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_provided": 22,
    "Isovaleryl-CoA_dehydrogenase_deficiency|IVD-related_disorder|not_specified": 1,
    "IVD-related_disorder": 7,
    "IVD-related_disorder|Inborn_genetic_diseases|Isovaleryl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Isovaleryl-CoA_dehydrogenase_deficiency|IVD-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Isovaleryl-CoA_dehydrogenase_deficiency|not_specified": 2,
    "not_specified|Isovaleryl-CoA_dehydrogenase_deficiency|not_provided": 2,
    "not_provided|Isovaleric_acidemia|_type_I|Isovaleryl-CoA_dehydrogenase_deficiency": 1,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Isovaleryl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|Isovaleryl-CoA_dehydrogenase_deficiency": 1,
    "IVD-related_disorder|Inborn_genetic_diseases|not_provided|Isovaleryl-CoA_dehydrogenase_deficiency": 1,
    "Isovaleryl-CoA_dehydrogenase_deficiency|IVD-related_disorder": 2,
    "Inborn_genetic_diseases|Isovaleryl-CoA_dehydrogenase_deficiency|not_specified": 2,
    "Isovaleryl-CoA_dehydrogenase_deficiency|not_provided|not_specified|IVD-related_disorder": 1,
    "IVD-related_disorder|not_specified|not_provided|Isovaleryl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|Isovaleryl-CoA_dehydrogenase_deficiency|Isovaleric_acidemia|_type_III": 1,
    "not_provided|Isovaleryl-CoA_dehydrogenase_deficiency|not_specified|IVD-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|not_provided": 3,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type": 30,
    "not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type|Ehlers-Danlos_syndrome|_musculocontractural_type_1": 1,
    "not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype": 23,
    "Ehlers-Danlos_syndrome|_musculocontractural_type": 80,
    "Cardiovascular_phenotype|not_specified|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_1": 13,
    "Cardiovascular_phenotype|CHST14-related_disorder": 2,
    "not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|Ehlers-Danlos_syndrome|_musculocontractural_type_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type": 6,
    "not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type": 2,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype|not_specified": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|Ehlers-Danlos_syndrome|_musculocontractural_type_1": 3,
    "Ehlers-Danlos_syndrome|_musculocontractural_type_1|Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|CHST14-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type|not_specified|not_provided": 1,
    "CHST14-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type|CHST14-related_disorder": 1,
    "not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|not_provided|Cardiovascular_phenotype": 3,
    "CHST14-related_disorder|Ehlers-Danlos_syndrome|_musculocontractural_type|Ehlers-Danlos_syndrome|_musculocontractural_type_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_musculocontractural_type|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|_musculocontractural_type": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|_musculocontractural_type|Ehlers-Danlos_syndrome|_musculocontractural_type_1": 1,
    "Ehlers-Danlos_syndrome|_musculocontractural_type|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_musculocontractural_type_1": 1,
    "Cardiofacioneurodevelopmental_syndrome": 3,
    "Microcephaly_4|_primary|_autosomal_recessive": 78,
    "Microcephaly_4|_primary|_autosomal_recessive|not_provided": 13,
    "not_provided|Microcephaly_4|_primary|_autosomal_recessive|not_specified|Primary_Microcephaly|_Recessive": 1,
    "KNL1-related_disorder": 16,
    "not_provided|Microcephaly_4|_primary|_autosomal_recessive|not_specified": 3,
    "not_provided|Microcephaly_4|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_specified": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|not_provided|not_specified": 2,
    "not_provided|KNL1-related_disorder": 2,
    "not_specified|Primary_Microcephaly|_Recessive|not_provided": 1,
    "not_provided|Microcephaly_4|_primary|_autosomal_recessive": 8,
    "not_provided|Inborn_genetic_diseases|Microcephaly_4|_primary|_autosomal_recessive": 1,
    "not_provided|not_specified|KNL1-related_disorder|Primary_Microcephaly|_Recessive": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_specified|not_provided": 3,
    "Microcephaly_4|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 2,
    "Microcephaly_4|_primary|_autosomal_recessive|not_specified|not_provided": 5,
    "Microcephaly_4|_primary|_autosomal_recessive|KNL1-related_disorder": 2,
    "Microcephaly_4|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "KNL1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Microcephaly_4|_primary|_autosomal_recessive|not_provided": 2,
    "Microcephaly_4|_primary|_autosomal_recessive|not_specified": 3,
    "Microcephaly_4|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_provided|not_specified": 2,
    "KNL1-related_disorder|Microcephaly_4|_primary|_autosomal_recessive": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|Primary_Microcephaly|_Recessive|not_provided": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "KNL1-related_disorder|not_provided|Primary_Microcephaly|_Recessive": 1,
    "KNL1-related_disorder|Microcephaly_4|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|not_specified|Microcephaly_4|_primary|_autosomal_recessive": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|KNL1-related_disorder|Microcephaly_4|_primary|_autosomal_recessive": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|not_provided|KNL1-related_disorder": 1,
    "KNL1-related_disorder|Microcephaly_4|_primary|_autosomal_recessive|not_specified|not_provided": 1,
    "not_specified|not_provided|Microcephaly_4|_primary|_autosomal_recessive": 1,
    "Microcephaly_4|_primary|_autosomal_recessive|KNL1-related_disorder|not_provided": 1,
    "KNL1-related_disorder|not_specified": 3,
    "Breast_cancer|_susceptibility_to|_in_BRCA1_and_BRCA2_carriers|not_provided": 1,
    "RAD51-related_disorder": 7,
    "Mirror_movements_2": 5,
    "not_provided|RAD51-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|RAD51-related_disorder": 1,
    "RAD51-related_disorder|Inborn_genetic_diseases": 2,
    "RAD51-related_disorder|not_provided": 5,
    "RAD51-related_disorder|Familial_cancer_of_breast": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_R": 1,
    "not_provided|Fanconi_anemia_complementation_group_R": 1,
    "Familial_cancer_of_breast|Hereditary_cancer|not_provided|RAD51-related_disorder|not_specified": 1,
    "Fanconi_anemia_complementation_group_R": 4,
    "RAD51-related_disorder|not_provided|Hereditary_cancer": 1,
    "Mirror_movements_2|Familial_cancer_of_breast": 1,
    "not_provided|RAD51-related_disorder|Fanconi_anemia_complementation_group_R|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|RAD51-related_disorder": 1,
    "not_provided|DNAJC17-related_disorder": 5,
    "DNAJC17-related_disorder|not_provided": 3,
    "not_provided|Hydrocephalus|_nonsyndromic|_autosomal_recessive_1": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_9": 8,
    "not_specified|Cholestasis|_progressive_familial_intrahepatic|_9": 1,
    "ZFYVE19-related_disorder": 3,
    "DLL4-related_disorder|not_provided": 4,
    "Adams-Oliver_syndrome_6": 17,
    "Adams-Oliver_syndrome|Adams-Oliver_syndrome_6": 6,
    "Inborn_genetic_diseases|not_provided|Adams-Oliver_syndrome_6": 1,
    "DLL4-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|DLL4-related_disorder": 3,
    "DLL4-related_disorder|Adams-Oliver_syndrome|Adams-Oliver_syndrome_6": 1,
    "DLL4-related_disorder": 7,
    "Inborn_genetic_diseases|not_provided|DLL4-related_disorder": 1,
    "Inborn_genetic_diseases|DLL4-related_disorder|Focal_segmental_glomerulosclerosis_9|Adams-Oliver_syndrome_6": 1,
    "Adams-Oliver_syndrome_6|not_provided": 1,
    "INO80-related_disorder": 15,
    "See_cases|INO80-related_disorder": 1,
    "Primary_microcephaly|Seizure|Intellectual_disability|INO80-related_immunodeficiency": 2,
    "INO80-related_disorder|not_provided": 3,
    "not_specified|INO80-related_disorder": 3,
    "not_provided|INO80-related_disorder": 2,
    "INO80-related_disorder|not_specified": 1,
    "Spastic_ataxia_9|_autosomal_recessive": 1,
    "CHP1-related_disorder": 2,
    "Microcephaly|_seizures|_and_developmental_delay": 27,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFAF1-related_disorder|not_specified|not_provided": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_11|not_provided": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_11": 2,
    "NDUFAF1-related_disorder": 1,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_11": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_11": 2,
    "not_provided|not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_11": 1,
    "not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_11": 1,
    "NDUFAF1-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_11": 1,
    "46|XX_disorder_of_sex_development": 1,
    "Premature_ovarian_failure_26": 3,
    "MGA_related_disorder": 3,
    "Nephronophthisis_20": 23,
    "MAPKBP1-related_disorder": 16,
    "Nephronophthisis_20|not_provided|Inborn_genetic_diseases": 1,
    "MAPKBP1-related_disorder|not_provided": 10,
    "not_provided|MAPKBP1-related_disorder": 6,
    "Inborn_genetic_diseases|Nephronophthisis_20": 1,
    "MAPKBP1-related_disorder|Nephronophthisis_20": 1,
    "not_specified|MAPKBP1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MAPKBP1-related_disorder|Inborn_genetic_diseases": 2,
    "Nephronophthisis_20|not_provided": 2,
    "MAPKBP1-related_disorder|not_provided|Nephronophthisis_20": 1,
    "not_provided|Nephronophthisis_20": 1,
    "not_provided|not_specified|MAPKBP1-related_disorder|Nephronophthisis_20": 1,
    "not_specified|not_provided|MAPKBP1-related_disorder": 1,
    "MAPKBP1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|MAPKBP1-related_disorder|not_provided": 1,
    "not_provided|MAPKBP1-related_disorder|Nephronophthisis_20": 1,
    "MAPKBP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "JMJD7-related_disorder": 5,
    "JMJD7-PLA2G4B-related_disorder": 33,
    "PLA2G4B-related_disorder": 7,
    "not_provided|JMJD7-PLA2G4B-related_disorder": 1,
    "JMJD7-PLA2G4B-related_disorder|not_specified": 1,
    "JMJD7-PLA2G4B-related_disorder|not_provided|Neurodevelopmental_disorder": 1,
    "SPTBN5-related_disorder": 39,
    "SPTBN5-related_disorder|not_specified": 6,
    "SPTBN5-related_disorder|not_provided": 3,
    "not_specified|SPTBN5-related_disorder": 4,
    "not_provided|SPTBN5-related_disorder": 2,
    "not_specified|Intellectual_disability|_moderate|Autism|Premature_birth|Autistic_behavior|Delayed_speech_and_language_development": 1,
    "not_specified|Autism|Intellectual_disability|_moderate|Delayed_speech_and_language_development|Premature_birth|Autistic_behavior": 1,
    "not_provided|not_specified|SPTBN5-related_disorder": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive": 12,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Limb-girdle_muscular_dystrophy|_recessive": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1064,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 9,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 95,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Inborn_genetic_diseases": 9,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 6,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 14,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided": 15,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 38,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 11,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 7,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Myopathy|_centronuclear|_2": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 27,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy": 4,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 9,
    "Abnormality_of_the_musculature|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 77,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified": 11,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 43,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy": 4,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 6,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 12,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 7,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|CAPN3-related_disorder|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 13,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Inborn_genetic_diseases": 4,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 5,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 21,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|not_provided": 1,
    "Familial_idiopathic_inflammatory_myopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "CAPN3-related_disorder": 2,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 10,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|CAPN3-related_disorder|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|not_provided": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Elevated_circulating_creatine_kinase_concentration|Difficulty_walking|Progressive_spinal_muscular_atrophy|Absent_muscle_fiber_calpain-3|Migraine|EMG:_neuropathic_changes|Positive_Romberg_sign|Paresthesia|Muscle_weakness|Myopathy|Absent_Achilles_reflex|CAPN3-related_disorder|Limb-girdle_muscular_dystrophy|_recessive|Muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Congenital_muscular_dystrophy|Shoulder_girdle_muscle_weakness|Limb-girdle_muscle_weakness|Lower-limb_joint_contracture|Cardiac_arrhythmia|Elbow_flexion_contracture|Calf_muscle_hypertrophy|EMG:_myopathic_abnormalities|See_cases": 1,
    "not_provided|not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|not_specified": 2,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided": 2,
    "CAPN3-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 3,
    "CAPN3-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 3,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 1,
    "Absent_Achilles_reflex|Myopathy|Muscle_weakness": 1,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified": 1,
    "Limb-girdle_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Abnormality_of_the_musculature": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|See_cases": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Abnormality_of_the_musculature": 2,
    "Limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Abnormality_of_the_musculature": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|CAPN3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|CAPN3-related_disorder": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided": 2,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|CAPN3-related_disorder|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "CAPN3-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Cardiac_arrhythmia|Lower-limb_joint_contracture|Muscle_weakness|Muscular_dystrophy|Elbow_flexion_contracture": 1,
    "Qualitative_or_quantitative_defects_of_calpain|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "not_specified|not_provided|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "CAPN3-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|CAPN3-related_disorder|not_provided": 1,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|CAPN3-related_disorder": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified|not_provided": 1,
    "CAPN3-related_disorder|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Abnormality_of_the_musculature": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Limb-girdle_muscular_dystrophy|_recessive|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|CAPN3-related_disorder": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Abnormality_of_the_musculature": 2,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Abnormality_of_the_musculature": 2,
    "Paresthesia|EMG:_neuropathic_changes|Migraine|Difficulty_walking|Positive_Romberg_sign|Elevated_circulating_creatine_kinase_concentration|Absent_muscle_fiber_calpain-3|Progressive_spinal_muscular_atrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Abnormality_of_the_musculature|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 2,
    "not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|CAPN3-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Limb-girdle_muscular_dystrophy|_recessive|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_specified": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_disease|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_provided": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|See_cases": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified|Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Myositis|_eosinophilic": 1,
    "not_provided|Limb-girdle_muscular_dystrophy|_recessive|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive|not_provided": 1,
    "CAPN3-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A": 1,
    "Muscular_dystrophy|_limb-girdle|_autosomal_dominant_4|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2A|Limb-girdle_muscular_dystrophy|_recessive|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "not_specified|STARD9-related_disorder": 5,
    "STARD9-related_disorder": 41,
    "not_provided|STARD9-related_disorder": 7,
    "not_specified|STARD9-related_disorder|not_provided": 1,
    "STARD9-related_disorder|not_provided": 2,
    "STARD9-related_intellectual_disabilities_with_blindness": 1,
    "STARD9-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|STARD9-related_disorder": 1,
    "STARD9-related_Intellectual_Disability": 1,
    "Congenital_dyserythropoietic_anemia|_type_I": 47,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_I": 11,
    "Congenital_dyserythropoietic_anemia|_type_I|not_provided": 18,
    "not_provided|Anemia|_congenital_dyserythropoietic|_type_1a": 27,
    "Anemia|_congenital_dyserythropoietic|_type_1a": 82,
    "Inborn_genetic_diseases|Anemia|_congenital_dyserythropoietic|_type_1a": 12,
    "CDAN1-related_disorder": 9,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Inborn_genetic_diseases": 17,
    "not_provided|Inborn_genetic_diseases|Anemia|_congenital_dyserythropoietic|_type_1a": 2,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Inborn_genetic_diseases|not_provided": 4,
    "Congenital_dyserythropoietic_anemia|_type_I|not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|not_specified": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_provided": 23,
    "not_specified|not_provided|Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a": 3,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 8,
    "not_provided|CDAN1-related_disorder": 7,
    "not_specified|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a|not_provided": 13,
    "not_specified|CDAN1-related_disorder|Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a|not_provided": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I|not_provided": 3,
    "Congenital_dyserythropoietic_anemia|_type_I|not_specified|not_provided|Anemia|_congenital_dyserythropoietic|_type_1a": 5,
    "not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|CDAN1-related_disorder|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Inborn_genetic_diseases|Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I|not_provided": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_specified|not_provided": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I": 5,
    "Congenital_dyserythropoietic_anemia|_type_I|not_specified|not_provided": 1,
    "CDAN1-related_disorder|Congenital_dyserythropoietic_anemia|_type_I|not_provided": 1,
    "not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_specified|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 2,
    "not_provided|Inborn_genetic_diseases|Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "not_provided|Inborn_genetic_diseases|CDAN1-related_disorder|Anemia|_congenital_dyserythropoietic|_type_1a": 1,
    "Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a|CDAN1-related_disorder|not_provided": 2,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_provided|CDAN1-related_disorder|Congenital_dyserythropoietic_anemia|_type_I": 3,
    "not_provided|CDAN1-related_disorder|Anemia|_congenital_dyserythropoietic|_type_1a": 2,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_I|not_specified|Anemia|_congenital_dyserythropoietic|_type_1a": 1,
    "Congenital_dyserythropoietic_anemia|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Anemia|_congenital_dyserythropoietic|_type_1a": 2,
    "not_provided|CDAN1-related_disorder|Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a": 1,
    "Congenital_dyserythropoietic_anemia|_type_I|Inborn_genetic_diseases": 1,
    "not_specified|Anemia|_congenital_dyserythropoietic|_type_1a|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "CDAN1-related_disorder|not_provided": 3,
    "Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a|not_provided|Inborn_genetic_diseases": 1,
    "CDAN1-related_disorder|not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|Inborn_genetic_diseases": 1,
    "Congenital_dyserythropoietic_anemia|_type_I|not_provided|Anemia|_congenital_dyserythropoietic|_type_1a": 2,
    "Inborn_genetic_diseases|Anemia|_congenital_dyserythropoietic|_type_1a|not_provided": 1,
    "not_provided|not_specified|Anemia|_congenital_dyserythropoietic|_type_1a": 1,
    "CDAN1-related_disorder|Anemia|_congenital_dyserythropoietic|_type_1a|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 2,
    "Anemia|_congenital_dyserythropoietic|_type_1a|CDAN1-related_disorder|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_specified": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I|not_specified|not_provided": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_anemia|CDAN1-related_disorder|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a": 2,
    "Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a": 2,
    "not_provided|not_specified|Congenital_dyserythropoietic_anemia|_type_I|Anemia|_congenital_dyserythropoietic|_type_1a": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "CDAN1-related_disorder|not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|not_specified": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|CDAN1-related_disorder|not_provided": 1,
    "not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|CDAN1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|not_provided": 1,
    "Anemia|_congenital_dyserythropoietic|_type_1a|not_provided|Inborn_genetic_diseases": 2,
    "Anemia|_congenital_dyserythropoietic|_type_1a|Inborn_genetic_diseases|not_provided|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I|not_specified": 1,
    "not_provided|Anemia|_congenital_dyserythropoietic|_type_1a|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "CDAN1-related_disorder|Congenital_dyserythropoietic_anemia|_type_I": 1,
    "Spinocerebellar_ataxia_type_11": 53,
    "not_provided|Spinocerebellar_ataxia_type_11": 11,
    "Spinocerebellar_ataxia_type_11|not_provided": 12,
    "Spinocerebellar_ataxia_type_11|not_provided|not_specified": 1,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_11": 3,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_11|not_provided": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_11": 1,
    "not_provided|Spinocerebellar_ataxia_type_11|not_specified": 2,
    "not_specified|Spinocerebellar_ataxia_type_11|Inborn_genetic_diseases|not_provided": 1,
    "Spinocerebellar_ataxia_type_11|Inborn_genetic_diseases|not_specified|TTBK2-related_disorder|not_provided": 1,
    "TTBK2-related_disorder|not_specified|not_provided|Spinocerebellar_ataxia_type_11": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_11": 1,
    "not_specified|Spinocerebellar_ataxia_type_11|not_provided|TTBK2-related_disorder": 1,
    "not_provided|TTBK2-related_disorder": 2,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_11": 3,
    "Spinocerebellar_ataxia_type_11|TTBK2-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia_type_11|Inborn_genetic_diseases|not_provided": 2,
    "Spinocerebellar_ataxia_type_11|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_11|not_specified|TTBK2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Spinocerebellar_ataxia_type_11|not_provided|TTBK2-related_disorder": 1,
    "not_specified|Spinocerebellar_ataxia_type_11|not_provided": 1,
    "TTBK2-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|TTBK2-related_disorder|not_specified|not_provided": 1,
    "not_specified|TTBK2-related_disorder|not_provided|Spinocerebellar_ataxia_type_11": 1,
    "not_provided|Spinocerebellar_ataxia_type_11|Inborn_genetic_diseases|Spastic_ataxia": 1,
    "not_specified|Spinocerebellar_ataxia_type_11|TTBK2-related_disorder|not_provided": 1,
    "not_provided|UBR1-related_disorder|Inborn_genetic_diseases": 1,
    "UBR1-related_disorder|not_provided": 15,
    "Microcephaly|not_provided|UBR1-related_disorder": 1,
    "Johanson-Blizzard_syndrome": 25,
    "not_provided|Johanson-Blizzard_syndrome": 7,
    "UBR1-related_disorder|not_specified|not_provided": 2,
    "not_specified|Johanson-Blizzard_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|UBR1-related_disorder": 1,
    "UBR1-related_disorder": 7,
    "not_provided|UBR1-related_disorder": 6,
    "Johanson-Blizzard_syndrome|not_provided": 3,
    "Johanson-Blizzard_syndrome|Inborn_genetic_diseases": 1,
    "UBR1-related_disorder|not_specified|not_provided|Johanson-Blizzard_syndrome": 1,
    "Inborn_genetic_diseases|Johanson-Blizzard_syndrome": 1,
    "Johanson-Blizzard_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|Johanson-Blizzard_syndrome": 2,
    "UBR1-related_disorder|Johanson-Blizzard_syndrome": 1,
    "Inborn_genetic_diseases|Johanson-Blizzard_syndrome|not_provided": 1,
    "UBR1-related_disorder|Inborn_genetic_diseases|Johanson-Blizzard_syndrome": 1,
    "Hereditary_spherocytosis_type_5": 74,
    "EPB42-related_disorder|Hereditary_spherocytosis_type_5|not_provided": 2,
    "EPB42-related_disorder|not_provided|Hereditary_spherocytosis_type_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_5": 13,
    "Hereditary_spherocytosis_type_5|not_provided": 10,
    "Spherocytosis|_Recessive": 5,
    "EPB42-related_disorder|Inborn_genetic_diseases|Hereditary_spherocytosis_type_5": 1,
    "not_provided|Hereditary_spherocytosis_type_5": 12,
    "not_provided|Inborn_genetic_diseases|Hereditary_spherocytosis_type_5": 3,
    "Hereditary_spherocytosis_type_5|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_5|EPB42-related_disorder|not_provided": 1,
    "Hereditary_spherocytosis_type_5|not_specified|not_provided": 4,
    "not_specified|Hereditary_spherocytosis_type_5|not_provided": 2,
    "EPB42-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spherocytosis_type_5": 1,
    "not_provided|Spherocytosis|_Recessive": 1,
    "not_provided|Hereditary_spherocytosis_type_5|not_specified": 3,
    "Hereditary_spherocytosis_type_5|not_provided|EPB42-related_disorder": 1,
    "Hereditary_spherocytosis_type_5|not_provided|not_specified": 2,
    "not_specified|not_provided|Hereditary_spherocytosis_type_5": 1,
    "not_provided|Hereditary_spherocytosis_type_5|Inborn_genetic_diseases": 1,
    "EPB42-related_disorder|Hereditary_spherocytosis_type_5": 2,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_5|not_provided": 1,
    "not_specified|Hereditary_spherocytosis_type_5": 1,
    "Acral_peeling_skin_syndrome": 39,
    "Acral_peeling_skin_syndrome|not_provided": 17,
    "TGM5-related_disorder": 5,
    "not_provided|Acral_peeling_skin_syndrome|TGM5-related_disorder": 1,
    "Inborn_genetic_diseases|Acral_peeling_skin_syndrome": 2,
    "TGM5-related_disorder|Acral_peeling_skin_syndrome|not_provided": 2,
    "TGM5-related_disorder|not_provided|Acral_peeling_skin_syndrome": 2,
    "Acral_peeling_skin_syndrome|TGM5-related_disorder|not_provided": 2,
    "not_provided|Acral_peeling_skin_syndrome": 4,
    "TGM5-related_disorder|Acral_peeling_skin_syndrome": 1,
    "not_provided|TGM5-related_disorder|Acral_peeling_skin_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Acral_peeling_skin_syndrome|TGM5-related_disorder": 1,
    "Acral_peeling_skin_syndrome|Peeling_skin_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Acral_peeling_skin_syndrome": 1,
    "TGM5-related_disorder|Inborn_genetic_diseases|not_provided|Acral_peeling_skin_syndrome": 1,
    "not_specified|ZSCAN29-related_disorder": 1,
    "ZSCAN29-related_disorder": 7,
    "Microcephaly_and_chorioretinopathy_3": 3,
    "Inborn_genetic_diseases|not_provided|not_specified|TUBGCP4-related_disorder": 1,
    "TUBGCP4-related_disorder|not_provided": 2,
    "Microcephaly_and_chorioretinopathy_3|not_provided": 5,
    "TUBGCP4-related_disorder": 2,
    "not_provided|Microcephaly_and_chorioretinopathy_3": 2,
    "not_provided|TUBGCP4-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Microcephaly_and_chorioretinopathy_3|not_specified|not_provided": 1,
    "Autosomal_recessive_chorioretinopathy-microcephaly_syndrome|TUBGCP4-related_disorder|Microcephaly_and_chorioretinopathy_3|not_provided": 1,
    "not_provided|Microcephaly_and_chorioretinopathy_3|Inborn_genetic_diseases": 1,
    "TP53BP1-related_disorder": 2,
    "MAP1A-related_disorder": 10,
    "MAP1A-related_disorder|not_specified": 1,
    "not_specified|MAP1A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16": 21,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16": 7,
    "STRC-related_disorder": 11,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16": 1,
    "Rare_genetic_deafness|STRC-related_disorder|not_provided": 1,
    "STRC-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16|Deafness-infertility_syndrome|Spermatogenic_failure_7": 1,
    "not_specified|STRC-related_disorder|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16|not_specified": 3,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_16|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16|STRC-related_disorder": 1,
    "not_provided|STRC-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|Rare_genetic_deafness": 3,
    "STRC-related_disorder|not_specified|Spermatogenic_failure_7|Autosomal_recessive_nonsyndromic_hearing_loss_16|Deafness-infertility_syndrome|not_provided": 1,
    "Spermatogenic_failure_7|Deafness-infertility_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_16": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_16": 5,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_16": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided|Rare_genetic_deafness": 1,
    "STRC-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_16|Rare_genetic_deafness|not_provided": 1,
    "Deafness-infertility_syndrome|Spermatogenic_failure_7|Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|STRC-related_disorder": 1,
    "Deafness-infertility_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_16": 1,
    "Spermatogenic_failure_7|Autosomal_recessive_nonsyndromic_hearing_loss_16|Deafness-infertility_syndrome|Inborn_genetic_diseases": 2,
    "Deafness-infertility_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_16|Spermatogenic_failure_7|Rare_genetic_deafness|STRC-related_disorder|not_provided": 1,
    "STRC-related_disorder|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_specified": 2,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_16|Spermatogenic_failure_7|Deafness-infertility_syndrome|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_16": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided|not_specified": 1,
    "STRC-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided": 1,
    "STRC-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided": 3,
    "STRC-related_disorder|Rare_genetic_deafness|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_specified|STRC-related_disorder": 1,
    "Deafness-infertility_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_16|Spermatogenic_failure_7|not_provided|STRC-related_disorder|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided|STRC-related_disorder": 1,
    "STRC-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_16|not_provided|not_specified|Deafness-infertility_syndrome|Spermatogenic_failure_7": 1,
    "STRC-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_16|Rare_genetic_deafness": 1,
    "STRC-related_disorder|not_specified|not_provided": 1,
    "STRC-related_disorder|not_specified": 1,
    "nonsyndromic_sensorineural_hearing_loss": 2,
    "Deafness-infertility_syndrome|Rare_genetic_deafness": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_16": 2,
    "CATSPER2-related_condition|not_provided": 1,
    "not_specified|Rare_genetic_deafness|not_provided": 1,
    "not_provided|Infertility_disorder": 1,
    "PDIA3-related_disorder|not_provided": 3,
    "not_provided|PDIA3-related_disorder": 1,
    "PDIA3-related_disorder": 4,
    "FRMD5-related_condition|not_provided": 1,
    "FRMD5-related_condition": 1,
    "Neurodevelopmental_disorder_with_eye_movement_abnormalities_and_ataxia|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_eye_movement_abnormalities_and_ataxia|Neurodevelopmental_delay": 1,
    "Neurodevelopmental_disorder_with_eye_movement_abnormalities_and_ataxia": 9,
    "See_cases|Neurodevelopmental_disorder_with_eye_movement_abnormalities_and_ataxia": 3,
    "Hereditary_spastic_paraplegia_11": 2261,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11": 5,
    "SPG11-related_disorder": 7,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 11,
    "not_provided|Hereditary_spastic_paraplegia_11": 72,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 99,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 96,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 48,
    "Hereditary_spastic_paraplegia_11|not_provided": 63,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis": 1,
    "not_specified|Hereditary_spastic_paraplegia_11": 6,
    "not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_11": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11": 16,
    "Hereditary_spastic_paraplegia_11|SPG11-related_disorder": 11,
    "Hereditary_spastic_paraplegia_11|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "SPG11-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 4,
    "Hereditary_spastic_paraplegia_11|not_specified|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 10,
    "Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 9,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 17,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "SPG11-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "SPG11-related_disorder|Hereditary_spastic_paraplegia_11": 5,
    "Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 4,
    "SPG11-related_disorder|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "not_specified|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|not_specified|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|not_provided": 8,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Metabolic_disease|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Abnormal_central_motor_function": 1,
    "SPG11-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|Spastic_Paraplegia|_Recessive|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided": 6,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 3,
    "not_provided|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 6,
    "Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 4,
    "SPG11-related_disorder|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|SPG11-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11": 3,
    "Early-onset_Parkinson_disease_20|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia_11|SPG11-related_disorder|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 2,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 9,
    "See_cases|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 2,
    "Spastic_Paraplegia|_Recessive|not_specified|SPG11-related_disorder|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 2,
    "Amyotrophic_lateral_sclerosis_type_5|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|See_cases": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Amyotrophic_lateral_sclerosis_type_5": 2,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_provided": 3,
    "Hereditary_spastic_paraplegia|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia_11": 3,
    "Inborn_genetic_diseases|SPG11-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 4,
    "Spastic_Paraplegia|_Recessive|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|SPG11-related_disorder|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "SPG11-related_disorder|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|not_specified": 9,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|SPG11-related_spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|Juvenile_amyotrophic_lateral_sclerosis|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|not_provided": 3,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Inborn_genetic_diseases": 6,
    "SPG11-related_disorder|not_provided|Hereditary_spastic_paraplegia_11|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 5,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|not_provided": 6,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|not_specified|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "not_specified|SPG11-related_disorder|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|not_specified|not_provided": 2,
    "Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Juvenile_amyotrophic_lateral_sclerosis|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis|Generalized_hyperreflexia|Spastic_paraparesis|Difficulty_walking|Gait_disturbance": 1,
    "SPG11-related_disorder|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_provided": 3,
    "Abnormal_brain_morphology|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "SPG11-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Intellectual_disability|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|not_specified": 1,
    "Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "SPG11-related_disorder|Hereditary_spastic_paraplegia_11|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified|not_provided": 2,
    "not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Amyotrophic_lateral_sclerosis_type_5": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_11": 2,
    "not_specified|Hereditary_spastic_paraplegia_11|SPG11-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_provided": 2,
    "Hereditary_spastic_paraplegia_11|Spastic_Paraplegia|_Recessive": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_11|Juvenile_amyotrophic_lateral_sclerosis|Charcot-Marie-Tooth_disease_axonal_type_2X": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Juvenile_amyotrophic_lateral_sclerosis|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neurofibromatosis|_type_1|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|SPG11-related_disorder|not_specified|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia_11": 2,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "not_provided|Generalized_hyperreflexia|Difficulty_walking|Gait_disturbance|Spastic_paraparesis|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Abnormal_central_motor_function": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|SPG11-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|not_specified|SPG11-related_disorder|not_provided": 1,
    "SPG11-related_spastic_paraplegia": 1,
    "SPG11-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia|SPG11-related_disorder|Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|not_specified": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|SPG11-related_disorder|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|not_provided|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_provided|not_specified|Amyotrophic_lateral_sclerosis": 1,
    "SPG11-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|not_provided|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|not_provided": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5": 1,
    "SPG11-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|SPG11-related_disorder|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia_11|not_specified": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Amyotrophic_lateral_sclerosis|not_specified|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|SPG11-related_disorder|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified|Hereditary_spastic_paraplegia_11|not_provided|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|SPG11-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_5|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11": 2,
    "Hereditary_spastic_paraplegia|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "SPG11-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis_type_5|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "SPG11-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|not_provided|See_cases": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|SPG11-related_disorder|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|not_specified|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|SPG11-related_disorder|not_specified|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Neurofibromatosis|_type_1|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_11": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis": 1,
    "Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|not_provided": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Cerebral_amyloid_angiopathy|_APP-related": 1,
    "Hereditary_spastic_paraplegia_11|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_11": 1,
    "SPG11-related_disorder|Hereditary_spastic_paraplegia_11|Intellectual_disability|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Inborn_genetic_diseases": 1,
    "Spastic_ataxia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Hereditary_spastic_paraplegia_11|SPG11-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|not_specified": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2X|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_5|Hereditary_spastic_paraplegia_11|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Hereditary_spastic_paraplegia_11|not_specified|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia": 1,
    "Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia|Charcot-Marie-Tooth_disease_axonal_type_2X|Hereditary_spastic_paraplegia_11": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11": 1,
    "Amyotrophic_lateral_sclerosis_type_5|not_specified|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_11|Amyotrophic_lateral_sclerosis_type_5|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "Hereditary_spastic_paraplegia_11|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|SPG11-related_disorder|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia|Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia_11": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_5|not_provided|Hereditary_spastic_paraplegia_11|Charcot-Marie-Tooth_disease_axonal_type_2X": 1,
    "PATL2-related_disorder": 9,
    "Oocyte_maturation_defect_4": 16,
    "Oocyte_maturation_defect_4|Oocyte_maturation_defect_2": 1,
    "not_provided|Oocyte_maturation_defect_4": 1,
    "Amyloidosis|_hereditary_systemic_6|Hypoproteinemia|_hypercatabolic": 7,
    "Hypoproteinemia|_hypercatabolic": 45,
    "Hypoproteinemia|_hypercatabolic|Familial_visceral_amyloidosis|_Ostertag_type": 3,
    "Familial_visceral_amyloidosis|_Ostertag_type|Hypoproteinemia|_hypercatabolic": 1,
    "Familial_visceral_amyloidosis|_Ostertag_type|Amyloidosis|_hereditary_systemic_6|Hypoproteinemia|_hypercatabolic": 1,
    "Hypoproteinemia|_hypercatabolic|Amyloidosis|_hereditary_systemic_6": 1,
    "Inborn_genetic_diseases|Hypoproteinemia|_hypercatabolic|Amyloidosis|_hereditary_systemic_6": 1,
    "Non-Hodgkin_lymphoma|Familial_visceral_amyloidosis|_Ostertag_type": 1,
    "B2M-related_condition|Hypoproteinemia|_hypercatabolic": 1,
    "Spermatogenic_failure_59": 2,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8": 11,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8|not_provided": 2,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8": 4,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8": 1,
    "Idiopathic_environmental_intolerance|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8|Inborn_genetic_diseases|Neuromuscular_disease|not_provided": 1,
    "not_specified|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_8": 1,
    "Thyroid_dyshormonogenesis_6": 100,
    "Thyroid_dyshormonogenesis_6|not_provided": 89,
    "not_provided|Thyroid_dyshormonogenesis_6": 81,
    "not_provided|Thyroid_dyshormonogenesis_6|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism": 2,
    "DUOX2-related_disorder": 10,
    "not_provided|DUOX2-related_disorder": 13,
    "Thyroid_dyshormonogenesis_6|not_specified": 2,
    "Thyroid_dyshormonogenesis_6|not_provided|DUOX2-related_disorder": 2,
    "Thyroid_dyshormonogenesis_6|not_provided|not_specified": 6,
    "not_provided|Thyroid_dyshormonogenesis_6|Inborn_genetic_diseases": 2,
    "Thyroid_dyshormonogenesis_6|not_specified|not_provided": 9,
    "DUOX2-related_disorder|not_provided": 9,
    "Nongoitrous_Euthyroid_Hyperthyrotropinemia|Thyroid_dyshormonogenesis_6": 1,
    "Inborn_genetic_diseases|not_provided|Thyroid_dyshormonogenesis_6": 4,
    "not_provided|not_specified|Thyroid_dyshormonogenesis_6": 3,
    "not_provided|Thyroid_dyshormonogenesis_6|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|not_specified": 1,
    "Inborn_genetic_diseases|Thyroid_dyshormonogenesis_6|not_provided": 7,
    "not_provided|Thyroid_dyshormonogenesis_6|Familial_thyroid_dyshormonogenesis": 1,
    "DUOX2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Thyroid_dyshormonogenesis_6": 1,
    "Thyroid_dyshormonogenesis_6|DUOX2-related_disorder|not_provided": 2,
    "not_specified|Thyroid_dyshormonogenesis_6": 2,
    "not_provided|Thyroid_dyshormonogenesis_6|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|DUOX2-related_disorder": 1,
    "not_specified|Thyroid_dyshormonogenesis_6|not_provided": 4,
    "not_provided|Thyroid_dyshormonogenesis_6|DUOX2-related_disorder": 2,
    "not_provided|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|Thyroid_dyshormonogenesis_6": 1,
    "not_provided|Thyroid_dyshormonogenesis_6|not_specified": 8,
    "DUOX2-related_disorder|Thyroid_dyshormonogenesis_6|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|not_provided|not_specified|Congenital_hypothyroidism": 1,
    "DUOX2-related_disorder|Thyroid_dyshormonogenesis_6|not_provided": 1,
    "not_provided|DUOX2-related_disorder|Thyroid_dyshormonogenesis_6": 2,
    "Thyroid_dyshormonogenesis_6|Congenital_hypothyroidism|not_provided": 1,
    "DUOX2-related_disorder|Nongoitrous_Euthyroid_Hyperthyrotropinemia|Genetic_transient_congenital_hypothyroidism|Familial_thyroid_dyshormonogenesis|Inborn_genetic_diseases|Congenital_hypothyroidism|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "Nongoitrous_Euthyroid_Hyperthyrotropinemia|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|not_provided|Thyroid_dyshormonogenesis_6|DUOX2-related_disorder": 1,
    "Genetic_transient_congenital_hypothyroidism|Familial_thyroid_dyshormonogenesis|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "not_specified|not_provided|Thyroid_dyshormonogenesis_6": 3,
    "DUOX2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "DUOX2-related_disorder|Meckel_syndrome|_type_11|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "not_provided|Thyroid_dyshormonogenesis_6|Nongoitrous_Euthyroid_Hyperthyrotropinemia": 1,
    "Thyroid_dyshormonogenesis_6|not_specified|not_provided|DUOX2-related_disorder": 1,
    "Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism": 1,
    "Inborn_genetic_diseases|Thyroid_dyshormonogenesis_6": 1,
    "DUOX2-related_disorder|not_provided|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|Thyroid_dyshormonogenesis_6": 1,
    "Familial_thyroid_dyshormonogenesis|DUOX2-related_disorder|Nongoitrous_Euthyroid_Hyperthyrotropinemia|Inborn_genetic_diseases|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "not_provided|Inborn_genetic_diseases|Thyroid_dyshormonogenesis_6": 1,
    "Thyroid_dyshormonogenesis_6|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|DUOX2-related_disorder": 1,
    "Thyroid_dyshormonogenesis_6|not_provided|Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|DUOX2-related_disorder": 1,
    "Thyroid_dyshormonogenesis_6|Inborn_genetic_diseases|not_provided": 1,
    "Genetic_transient_congenital_hypothyroidism|Familial_thyroid_dyshormonogenesis|Inborn_genetic_diseases|Congenital_hypothyroidism|not_provided|DUOX2-related_disorder|Thyroid_dyshormonogenesis_6": 1,
    "Familial_thyroid_dyshormonogenesis|Genetic_transient_congenital_hypothyroidism|Congenital_hypothyroidism|not_provided|Thyroid_dyshormonogenesis_6|not_specified": 1,
    "Thyroid_dyshormonogenesis_6|not_provided|Inborn_genetic_diseases": 1,
    "See_cases|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "DUOX2-related_disorder|not_provided|Thyroid_dyshormonogenesis_6": 1,
    "Thyroglobulin_synthesis_defect": 24,
    "Thyroglobulin_synthesis_defect|not_provided": 1,
    "not_specified|not_provided|DUOXA2-related_disorder|Thyroglobulin_synthesis_defect|Inborn_genetic_diseases|Congenital_hypothyroidism": 1,
    "not_specified|not_provided|Thyroglobulin_synthesis_defect": 3,
    "not_provided|Thyroglobulin_synthesis_defect|not_specified": 2,
    "Familial_thyroid_dyshormonogenesis|Thyroglobulin_synthesis_defect": 1,
    "DUOXA2-related_disorder": 1,
    "Congenital_hypothyroidism|not_specified|Inborn_genetic_diseases|not_provided|DUOXA2-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|DUOXA2-related_disorder": 1,
    "Familial_thyroid_dyshormonogenesis|Inborn_genetic_diseases|Thyroglobulin_synthesis_defect": 1,
    "DUOXA2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "DUOX1-related_disorder": 4,
    "Arginine:glycine_amidinotransferase_deficiency|not_provided": 14,
    "Arginine:glycine_amidinotransferase_deficiency": 415,
    "not_provided|Arginine:glycine_amidinotransferase_deficiency": 11,
    "Arginine:glycine_amidinotransferase_deficiency|Inborn_genetic_diseases": 7,
    "Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1|not_specified": 3,
    "Inborn_genetic_diseases|Arginine:glycine_amidinotransferase_deficiency|not_specified|Fanconi_renotubular_syndrome_1|not_provided": 2,
    "Arginine:glycine_amidinotransferase_deficiency|not_specified": 10,
    "Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency|not_provided": 1,
    "GATM-related_disorder|Inborn_genetic_diseases|not_specified|Arginine:glycine_amidinotransferase_deficiency": 1,
    "Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1": 41,
    "Inborn_genetic_diseases|Arginine:glycine_amidinotransferase_deficiency": 4,
    "Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency": 10,
    "GATM-related_disorder": 2,
    "not_specified|Arginine:glycine_amidinotransferase_deficiency": 5,
    "Arginine:glycine_amidinotransferase_deficiency|not_provided|Fanconi_renotubular_syndrome_1": 1,
    "GATM-related_disorder|not_provided|Arginine:glycine_amidinotransferase_deficiency": 1,
    "Arginine:glycine_amidinotransferase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Arginine:glycine_amidinotransferase_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Arginine:glycine_amidinotransferase_deficiency": 1,
    "not_provided|Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1": 6,
    "not_specified|Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1": 2,
    "Inborn_genetic_diseases|Arginine:glycine_amidinotransferase_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency": 1,
    "Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Arginine:glycine_amidinotransferase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1|Inborn_genetic_diseases": 2,
    "GATM-related_disorder|Arginine:glycine_amidinotransferase_deficiency": 2,
    "GATM-related_disorder|not_provided|not_specified|Arginine:glycine_amidinotransferase_deficiency|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1": 3,
    "not_provided|Arginine:glycine_amidinotransferase_deficiency|Inborn_genetic_diseases|not_specified|Fanconi_renotubular_syndrome_1": 1,
    "Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Arginine:glycine_amidinotransferase_deficiency|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency": 1,
    "not_specified|not_provided|Arginine:glycine_amidinotransferase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Arginine:glycine_amidinotransferase_deficiency": 2,
    "not_provided|Fanconi_renotubular_syndrome_1|Arginine:glycine_amidinotransferase_deficiency|Seizure": 1,
    "not_provided|not_specified|Arginine:glycine_amidinotransferase_deficiency": 1,
    "Inborn_genetic_diseases|Arginine:glycine_amidinotransferase_deficiency|Fanconi_renotubular_syndrome_1|not_specified": 1,
    "GATM-related_disorder|not_provided": 1,
    "not_provided|Arginine:glycine_amidinotransferase_deficiency|not_specified": 1,
    "Neurodevelopmental_disorder_with_hearing_loss_and_spasticity|not_provided": 2,
    "AFG2B-related_disorder": 1,
    "not_provided|Neurodevelopmental_disorder_with_hearing_loss_and_spasticity": 3,
    "Hearing_loss|_autosomal_recessive_119|Neurodevelopmental_disorder_with_hearing_loss_and_spasticity|SPATA5L1-related_disorder|SPATA5L1-associated_disorder|AFG2B-related_disorder|Inborn_genetic_diseases|not_provided|Neurodevelopmental_delay|See_cases": 1,
    "Hearing_loss|_autosomal_recessive_119|not_provided": 1,
    "Neurodevelopmental_disorder_with_hearing_loss_and_spasticity": 3,
    "SPATA5L1-associated_disorder": 3,
    "Inborn_genetic_diseases|AFG2B-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hearing_loss_and_spasticity|AFG2B-related_disorder|SPATA5L1-associated_disorder|not_provided|See_cases": 1,
    "Hearing_loss|_autosomal_recessive_119": 3,
    "Hearing_loss|_autosomal_recessive_119|Neurodevelopmental_disorder_with_hearing_loss_and_spasticity|not_provided": 1,
    "Neurodevelopmental_disorder_with_hearing_loss_and_spasticity|SPATA5L1-associated_disorder": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hearing_loss_and_spasticity|See_cases|not_provided": 1,
    "SPATA5L1-related_disorder|Inborn_genetic_diseases|not_provided|Neurodevelopmental_delay": 1,
    "Hermansky-Pudlak_syndrome_9": 145,
    "Hermansky-Pudlak_syndrome_9|Inborn_genetic_diseases": 9,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_9": 1,
    "Hermansky-Pudlak_syndrome_9|BLOC1S6-related_disorder": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_9": 3,
    "BLOC1S6-related_disorder|not_specified|Hermansky-Pudlak_syndrome_9": 1,
    "BLOC1S6-related_disorder": 2,
    "Hermansky-Pudlak_syndrome_9|not_provided": 1,
    "Hermansky-Pudlak_syndrome_9|Hermansky-Pudlak_syndrome": 2,
    "BLOC1S6-related_disorder|Hermansky-Pudlak_syndrome_9": 1,
    "Hermansky-Pudlak_syndrome_9|not_provided|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome_9|not_specified": 1,
    "not_provided|BLOC1S6-related_disorder|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_9": 1,
    "Autoinflammatory_syndrome|Hermansky-Pudlak_syndrome_9": 1,
    "not_specified|Hermansky-Pudlak_syndrome_9": 1,
    "not_provided|Hermansky-Pudlak_syndrome_9|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Hermansky-Pudlak_syndrome_9|Inborn_genetic_diseases": 1,
    "SQOR-related_disorder": 2,
    "not_specified|Sulfide_quinone_oxidoreductase_deficiency": 1,
    "Sulfide_quinone_oxidoreductase_deficiency": 2,
    "not_specified|SEMA6D-related_disorder": 1,
    "SEMA6D-related_disorder": 19,
    "Oculocutaneous_albinism_type_6|not_provided": 2,
    "Oculocutaneous_albinism_type_6": 6,
    "Skin/hair/eye_pigmentation|_variation_in|_4": 3,
    "SLC24A5-related_disorder|not_provided": 2,
    "Oculocutaneous_albinism_type_6|SLC24A5-related_disorder|not_provided": 1,
    "not_provided|SLC24A5-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Oculocutaneous_albinism_type_6": 1,
    "MYEF2-related_condition": 1,
    "not_provided|Bartter_disease_type_1": 56,
    "Bartter_disease_type_1": 162,
    "Bartter_disease_type_1|not_provided|Inborn_genetic_diseases|SLC12A1-related_disorder": 1,
    "Bartter_disease_type_1|Inborn_genetic_diseases": 11,
    "Bartter_disease_type_1|not_provided": 40,
    "Bartter_disease_type_1|Inborn_genetic_diseases|not_provided": 5,
    "Bartter_disease_type_1|SLC12A1-related_disorder|not_specified|not_provided": 1,
    "not_provided|SLC12A1-related_disorder|Bartter_disease_type_1": 3,
    "Inborn_genetic_diseases|not_provided|Bartter_disease_type_1": 7,
    "SLC12A1-related_disorder|Bartter_disease_type_1|not_provided": 1,
    "Inborn_genetic_diseases|Bartter_disease_type_1": 9,
    "SLC12A1-related_disorder|Inborn_genetic_diseases|not_provided|Bartter_disease_type_1": 1,
    "SLC12A1-related_disorder": 5,
    "Inborn_genetic_diseases|Bartter_disease_type_1|not_provided": 2,
    "Bartter_disease_type_1|not_specified": 2,
    "SLC12A1-related_disorder|not_provided": 2,
    "not_specified|Bartter_disease_type_1|not_provided": 2,
    "Bartter_disease_type_1|not_provided|not_specified": 1,
    "not_provided|SLC12A1-related_disorder": 3,
    "not_provided|Bartter_disease_type_1|Nephrocalcinosis|Nephrolithiasis": 1,
    "Bartter_disease_type_1|Bartter_syndrome|not_provided": 2,
    "Bartter_syndrome|not_provided|Bartter_disease_type_1": 1,
    "Bartter_disease_type_1|SLC12A1-related_disorder": 1,
    "not_provided|Bartter_disease_type_1|Inborn_genetic_diseases": 2,
    "Nephrocalcinosis|Nephrolithiasis|Bartter_disease_type_1|not_provided": 1,
    "not_specified|Bartter_disease_type_1": 2,
    "Inborn_genetic_diseases|SLC12A1-related_disorder": 1,
    "Bartter_disease_type_1|Nephrocalcinosis|Nephrolithiasis": 1,
    "not_provided|not_specified|Bartter_disease_type_1": 1,
    "Bartter_disease_type_1|Bartter_syndrome": 1,
    "Bartter_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Bartter_disease_type_1|SLC12A1-related_disorder|not_provided": 1,
    "Familial_hypokalemia-hypomagnesemia|Bartter_syndrome|Bartter_disease_type_1|not_specified": 1,
    "Bartter_disease_type_1|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Bartter_disease_type_1": 2,
    "not_provided|Bartter_disease_type_1|SLC12A1-related_disorder": 1,
    "Bartter_disease_type_1|not_provided|SLC12A1-related_disorder": 1,
    "SLC12A1-related_disorder|not_provided|Bartter_disease_type_1": 3,
    "Bartter_disease_type_1|not_provided|Bartter_syndrome": 1,
    "not_specified|not_provided|Bartter_disease_type_1": 4,
    "Bartter_disease_type_1|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Bartter_disease_type_3": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_pancreatic_carcinoma|Myhre_syndrome": 3,
    "Bone_marrow_failure_and_diabetes_mellitus_syndrome": 3,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Marfan_syndrome|Stiff_skin_syndrome|MASS_syndrome": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia": 4,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis|MASS_syndrome": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Marfan_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia|Ectopia_lentis|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Ectopia_lentis|Acromicric_dysplasia|MASS_syndrome": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome": 2,
    "Marfan_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Geleophysic_dysplasia|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Marfan_syndrome": 1,
    "Geleophysic_dysplasia|Ectopia_lentis|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Marfan_syndrome|Acromicric_dysplasia|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Ectopia_lentis|Stiff_skin_syndrome|Marfan_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome|MASS_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Geleophysic_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Acromicric_dysplasia|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|MASS_syndrome": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Marfan_syndrome": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_provided|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Acromicric_dysplasia|Marfan_syndrome": 1,
    "Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome": 3,
    "Acromicric_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|not_provided|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Stiff_skin_syndrome|Geleophysic_dysplasia|Ectopia_lentis|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia|MASS_syndrome": 1,
    "Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis|Acromicric_dysplasia|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis|Acromicric_dysplasia|MASS_syndrome": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis|Marfan_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|not_provided|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Ectopia_lentis|Stiff_skin_syndrome|Marfan_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia|MASS_syndrome": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 6,
    "Acromicric_dysplasia|Marfan_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome|not_provided": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Acromicric_dysplasia|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|not_provided|Acromicric_dysplasia|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome|not_provided|Acromicric_dysplasia": 1,
    "Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Stiff_skin_syndrome|Marfan_syndrome|Acromicric_dysplasia|MASS_syndrome": 2,
    "Stiff_skin_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Weill-Marchesani_syndrome": 3,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Geleophysic_dysplasia|Stiff_skin_syndrome|MASS_syndrome|Weill-Marchesani_syndrome|not_provided|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Stiff_skin_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 2,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|not_provided": 1,
    "Stiff_skin_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 2,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome": 2,
    "Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Acromicric_dysplasia|Ectopia_lentis|Stiff_skin_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Marfan_syndrome|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome": 1,
    "Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|MASS_syndrome": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided": 148,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1741,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 45,
    "Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|not_provided": 43,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome": 3,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 165,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided": 15,
    "Acromicric_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Marfan_syndrome": 8,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 70,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided": 2,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 158,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 118,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 4,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 14,
    "FBN1-related_disorder|not_provided|not_specified|Marfan_syndrome": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome": 17,
    "Cardiovascular_phenotype|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 9,
    "Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified": 71,
    "FBN1-related_disorder": 39,
    "Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis|Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|MASS_syndrome|not_provided|Acromicric_dysplasia": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 48,
    "Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome": 1,
    "Isolated_thoracic_aortic_aneurysm|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome|not_specified": 1,
    "Connective_tissue_disorder|not_provided|Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 13,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder": 1,
    "not_provided|Marfan_syndrome|FBN1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN1-related_disorder|Connective_tissue_disorder": 1,
    "Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Stiff_skin_syndrome|MASS_syndrome|Acromicric_dysplasia|Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|FBN1-related_disorder": 1,
    "Marfan_syndrome|not_specified": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified": 2,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "not_provided|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 11,
    "Acromicric_dysplasia": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome": 22,
    "FBN1-related_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|not_provided": 1,
    "Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 38,
    "Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "not_specified|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided": 10,
    "MASS_syndrome|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Marfan_syndrome|Cardiovascular_phenotype": 5,
    "Weill-Marchesani_syndrome|Geleophysic_dysplasia|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Geleophysic_dysplasia_2|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Connective_tissue_disorder": 2,
    "Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|not_provided": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_provided": 1,
    "Geleophysic_dysplasia|Acromicric_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome|not_specified": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 23,
    "Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Acromicric_dysplasia": 2,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Geleophysic_dysplasia_2|not_provided": 1,
    "not_provided|Marfan_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 44,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|not_provided": 5,
    "Marfan_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 12,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|not_provided": 1,
    "Mitral_regurgitation|Ectopia_lentis|High_palate|Tall_stature|Aortic_root_aneurysm|Protrusio_acetabuli|Dental_crowding": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|MASS_syndrome": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant": 2,
    "Stiff_skin_syndrome": 4,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|FBN1-related_disorder": 3,
    "not_provided|Cardiovascular_phenotype|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FBN1-related_disorder": 2,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided": 2,
    "Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia": 2,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided": 3,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Geleophysic_dysplasia_2|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|not_provided": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Weill-Marchesani_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified": 8,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Striae_distensae|Pulmonary_artery_dilatation|Mitral_valve_prolapse": 1,
    "not_provided|Isolated_thoracic_aortic_aneurysm|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|not_specified|Geleophysic_dysplasia": 1,
    "Acromicric_dysplasia|not_specified|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Weill-Marchesani_syndrome|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Connective_tissue_disorder": 1,
    "Marfan_syndrome|Myopathy|not_provided": 1,
    "not_provided|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome": 4,
    "Thoracic_aortic_aneurysm_or_dissection|Connective_tissue_dysplasia|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ascending_tubular_aorta_aneurysm|Joint_hypermobility|Tall_stature|Scoliosis|High_myopia|Aortic_aneurysm": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder": 9,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 3,
    "Isolated_thoracic_aortic_aneurysm|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|MARFAN_SYNDROME|_AUTOSOMAL_RECESSIVE|FBN1-related_disorder": 1,
    "Marfan_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|not_specified": 17,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Marfan_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Coronary_artery_dissection|Marfan_syndrome|_incomplete|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection|not_provided": 1,
    "Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 3,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome|not_specified|Acromicric_dysplasia|Stiff_skin_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|not_specified": 1,
    "Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|FBN1-related_disorder": 1,
    "Marfan_syndrome|FBN1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided|Weill-Marchesani_syndrome|Geleophysic_dysplasia": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|not_specified|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm|not_provided": 2,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm": 8,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided": 2,
    "Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Marfan_syndrome|Acromicric_dysplasia|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "Marfan_syndrome|Connective_tissue_disorder": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome": 7,
    "Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 2,
    "Abnormality_of_connective_tissue|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|not_provided": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|FBN1-related_disorder": 2,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Connective_tissue_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 3,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome": 2,
    "Aortic_dissection|Polycystic_liver_disease_1|Aortic_dilatation|Ascending_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Weill-Marchesani_syndrome|not_specified|not_provided": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 11,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Stiff_skin_syndrome": 1,
    "FBN1-related_disorder|not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|not_provided|Connective_tissue_disorder": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|not_specified": 1,
    "not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 10,
    "not_provided|Aortic_aneurysm|_familial_thoracic_2|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder|not_provided": 2,
    "Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "FBN1-related_disorder|not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Stiff_skin_syndrome|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|not_specified": 1,
    "Acromicric_dysplasia|not_specified|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Isolated_thoracic_aortic_aneurysm|Marfan_syndrome": 3,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|FBN1-related_disorder": 5,
    "Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|not_provided": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|not_specified|not_provided": 1,
    "Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2": 3,
    "Isolated_thoracic_aortic_aneurysm|not_provided": 1,
    "Aortic_dissection|not_provided": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "MARFAN_SYNDROME|_MILD_VARIABLE|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Connective_tissue_disorder|Acromicric_dysplasia": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome|not_specified|not_provided": 1,
    "FBN1-related_disorder|MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Acromicric_dysplasia|not_specified|Geleophysic_dysplasia|not_provided|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome": 1,
    "not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|not_specified|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 3,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder|not_specified|not_provided": 1,
    "Connective_tissue_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 4,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|FBN1-related_disorder": 2,
    "Isolated_thoracic_aortic_aneurysm|Congenital_scoliosis": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_provided|Marfan_syndrome": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Marfan_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided": 1,
    "Dolichocephaly|Pes_planus|Mitral_valve_prolapse|Scoliosis|High_palate|Myopia|Dilatation_of_the_ascending_aorta": 1,
    "Thoracic_aortic_aneurysm_or_dissection|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Isolated_thoracic_aortic_aneurysm": 4,
    "Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 5,
    "Thoracic_aortic_aneurysm_or_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome": 1,
    "Connective_tissue_disorder|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Marfan_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Stiff_skin_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|not_provided": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant": 1,
    "MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|FBN1-related_disorder": 1,
    "Acromicric_dysplasia|not_specified|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Connective_tissue_disorder|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided|Stiff_skin_syndrome|Acromicric_dysplasia|FBN1-related_disorder": 1,
    "Geleophysic_dysplasia_2|Marfan_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 3,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Stiff_skin_syndrome": 1,
    "Marfan_syndrome|not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia": 2,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Marfan_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN1-related_disorder|not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm": 1,
    "Geleophysic_dysplasia_2|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_scoliosis|Marfan_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 2,
    "Thoracic_aortic_aneurysm_or_dissection|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|See_cases|FBN1-related_disorder": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|Acromicric_dysplasia": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|MASS_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 11,
    "FBN1-related_disorder|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Marfan_syndrome|FBN1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Isolated_thoracic_aortic_aneurysm": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2": 3,
    "not_specified|Acromicric_dysplasia|not_provided|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder|Marfan_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Marfan_syndrome|Connective_tissue_disorder|not_provided": 1,
    "Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Marfan_syndrome|Ectopia_lentis|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "See_cases|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Marfan_syndrome|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN1-related_disorder|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder": 2,
    "Thoracic_aortic_disease": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome|FBN1-related_disorder": 1,
    "not_provided|FBN1-related_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|not_specified|FBN1-related_disorder": 2,
    "See_cases|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Marfan_syndrome|Congenital_contractural_arachnodactyly": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Cardiovascular_phenotype": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|MASS_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome": 1,
    "Ectopia_lentis|not_specified|FBN1-related_disorder|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|Stiff_skin_syndrome|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Weill-Marchesani_syndrome_2|_dominant|not_provided": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Marfan_syndrome": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 3,
    "Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia": 3,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FBN1-related_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Thoracic_aortic_aneurysm_or_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided|FBN1-related_disorder|Melanoma|Ischemic_stroke|Ectopia_lentis|Aortic_root_aneurysm|Dissecting_aortic_dilatation|Arachnodactyly|High_myopia|See_cases": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Marfan_syndrome|Stiff_skin_syndrome|MASS_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Marfan_syndrome": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 3,
    "Thoracic_aortic_aneurysm_or_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 3,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome": 1,
    "Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Thoracic_aortic_aneurysm_or_dissection|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified|not_provided": 1,
    "MASS_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 1,
    "Marfan_syndrome|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Geleophysic_dysplasia|Acromicric_dysplasia|Ectopia_lentis|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder|not_provided|Weill-Marchesani_syndrome|Stiff_skin_syndrome|MASS_syndrome": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|FBN1-related_disorder|not_provided": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_specified|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Cardiovascular_phenotype": 3,
    "Acromicric_dysplasia|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|not_provided": 1,
    "Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Acromicric_dysplasia": 2,
    "Geleophysic_dysplasia_2": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Tall_stature|Marfan_syndrome": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 2,
    "Geleophysic_dysplasia_2|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Metaphyseal_chondrodysplasia|Wide_mouth|Wide_nasal_bridge|Relative_macrocephaly|Short_stature|MASS_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia": 1,
    "Geleophysic_dysplasia_2|Acromicric_dysplasia": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Heart_disease": 1,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "not_provided|Marfan_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Acromicric_dysplasia": 1,
    "Weill-Marchesani_syndrome_2|_dominant": 2,
    "Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|not_provided": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Weill-Marchesani_syndrome|Stiff_skin_syndrome|Marfan_syndrome|not_specified|Ectopia_lentis|not_provided|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|MASS_syndrome|Isolated_ectopia_lentis": 1,
    "Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Marfan_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Connective_tissue_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Marfan_syndrome|FBN1-related_disorder": 2,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|not_provided": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Isolated_thoracic_aortic_aneurysm|Connective_tissue_disorder|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome": 1,
    "MASS_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|FBN1-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Weill-Marchesani_syndrome": 38,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Geleophysic_dysplasia|Ectopia_lentis|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Acromicric_dysplasia|MASS_syndrome|Stiff_skin_syndrome|FBN1-related_disorder": 1,
    "FBN1-related_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_provided|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Marfan_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_provided|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|See_cases|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_provided|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2": 2,
    "Marfan_syndrome|not_provided|not_specified|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|See_cases|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia_2": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|FBN1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2": 1,
    "FBN1-related_disorder|not_provided|Marfan_syndrome": 1,
    "Isolated_thoracic_aortic_aneurysm|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "FBN1-related_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Mitral_valve_prolapse|Lumbar_scoliosis|Myxomatous_mitral_valve_degeneration|High_palate|Disproportionate_tall_stature|not_provided": 1,
    "See_cases|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2": 1,
    "Marfan_syndrome|Cardiovascular_phenotype|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_provided|not_specified|FBN1-related_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|not_specified|Marfan_syndrome": 1,
    "Isolated_thoracic_aortic_aneurysm|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|not_provided|Geleophysic_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|Ectopia_lentis|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|MASS_syndrome": 1,
    "Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Weill-Marchesani_syndrome|Geleophysic_dysplasia|not_specified": 1,
    "FBN1-related_disorder|MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia": 1,
    "Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Abnormality_of_connective_tissue|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|FBN1-related_disorder|Weill-Marchesani_syndrome|Marfan_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|FBN1-related_disorder|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Geleophysic_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN1-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome": 1,
    "Marfan_syndrome|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome": 1,
    "FBN1-related_disorder|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant": 1,
    "not_provided|Marfan_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Marfan_syndrome|Neonatal_Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Familial_ectopia_lentis": 1,
    "Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Cardiovascular_phenotype": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|FBN1-related_disorder|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified": 1,
    "Neonatal_Marfan_syndrome": 4,
    "Connective_tissue_disorder|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Weill-Marchesani_syndrome|not_provided|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|not_specified|Acromicric_dysplasia": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|Familial_aortopathy": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_specified|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided": 1,
    "not_specified|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "not_specified|Marfan_syndrome|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Acromicric_dysplasia": 1,
    "Pes_planus|Myopia|Aortic_root_aneurysm|Pes_valgus|Ectopia_lentis|Scoliosis|Pectus_carinatum|Striae_distensae|Mitral_valve_prolapse": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Marfan_syndrome|not_provided|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Acromicric_dysplasia": 1,
    "Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_specified|not_provided|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Acromicric_dysplasia": 1,
    "Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Marfan_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|FBN1-related_disorder|not_provided": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|not_specified|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|not_specified|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN1-related_disorder|Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|not_specified|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Connective_tissue_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 4,
    "Marfan_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis|Congenital_aneurysm_of_ascending_aorta|MASS_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Disproportionate_tall_stature|FBN1-related_disorder": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Connective_tissue_disorder|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2": 1,
    "Isolated_thoracic_aortic_aneurysm|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|Acromicric_dysplasia|Geleophysic_dysplasia|not_specified|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Connective_tissue_disorder": 1,
    "Thoracic_aortic_aneurysm_or_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Stiff_skin_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|not_provided|not_specified": 1,
    "Geleophysic_dysplasia|Acromicric_dysplasia|FNB1_POLYMORPHISM|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|not_provided|not_specified|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Connective_tissue_disorder": 1,
    "Congenital_scoliosis": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|FBN1-related_disorder": 2,
    "Thoracic_aortic_aneurysm_or_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_specified|Stiff_skin_syndrome": 1,
    "Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Developmental_cataract": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MARFAN_SYNDROME|_SEVERE_CLASSIC": 1,
    "Marfan_syndrome|not_provided|Connective_tissue_disorder|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|not_provided|Connective_tissue_disorder|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|MARFAN_SYNDROME|_MILD": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome|FBN1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|not_provided": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MASS_syndrome": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided": 1,
    "Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome": 1,
    "Marfan_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome|Neonatal_Marfan_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|not_specified|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|MASS_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis|not_provided": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|MASS_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Neonatal_Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 2,
    "Thoracic_aortic_aneurysm_or_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN1-related_disorder|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|MASS_syndrome|not_specified|not_provided|Connective_tissue_disorder|Cardiovascular_phenotype|Acromicric_dysplasia": 1,
    "not_provided|not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 1,
    "not_specified|Geleophysic_dysplasia|Weill-Marchesani_syndrome|MASS_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|FBN1-related_disorder|Geleophysic_dysplasia|Acromicric_dysplasia|Weill-Marchesani_syndrome": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN1-related_disorder": 1,
    "Marfan_syndrome|Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Connective_tissue_disorder|Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|FBN1-related_disorder": 1,
    "Marfan_syndrome|_atypical|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Geleophysic_dysplasia|not_provided|Marfan_syndrome|Weill-Marchesani_syndrome|not_specified|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "not_specified|not_provided|Connective_tissue_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Marfan_syndrome|Acromicric_dysplasia|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN1-related_disorder": 1,
    "not_provided|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Marfan_syndrome|Connective_tissue_disorder": 1,
    "Marfan_syndrome|Isolated_thoracic_aortic_aneurysm|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "not_specified|not_provided|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Marfan_syndrome|not_specified": 2,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_provided": 1,
    "Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "not_specified|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Marfan_syndrome|Geleophysic_dysplasia|not_specified|not_provided|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided": 1,
    "not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|FBN1-related_disorder": 1,
    "FBN1-related_disorder|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm|FBN1-related_disorder|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia|Acromicric_dysplasia|Stiff_skin_syndrome|not_specified": 1,
    "Connective_tissue_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Congenital_scoliosis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_specified": 1,
    "Congenital_scoliosis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FBN1-related_disorder|MASS_syndrome|Geleophysic_dysplasia_2|Acromicric_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided|not_specified|Isolated_thoracic_aortic_aneurysm|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2": 1,
    "Marfan_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder": 1,
    "MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Marfan_syndrome|not_provided|See_cases|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|not_provided": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ectopia_lentis|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|MASS_syndrome|Stiff_skin_syndrome": 1,
    "MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Familial_aortopathy|not_provided": 1,
    "Cardiovascular_phenotype|Connective_tissue_disorder|not_provided": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Marfan_syndrome|Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|MASS_syndrome|Geleophysic_dysplasia_2|Acromicric_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|not_specified": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified": 1,
    "Connective_tissue_disorder|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided|not_specified": 1,
    "FBN1-related_disorder|Marfan_syndrome": 1,
    "Positive_thumb_sign|Tall_stature|Pectus_excavatum": 1,
    "not_specified|Marfan_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Thoracic_aortic_aneurysm_or_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Thoracic_aortic_aneurysm_or_dissection|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acromicric_dysplasia|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FBN1-related_disorder": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Acute_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|FBN1-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia": 1,
    "MASS_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia": 1,
    "FBN1-related_disorder|Connective_tissue_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Acromicric_dysplasia": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Mitral_valve_prolapse|Pes_planus|Arachnodactyly|Aortic_aneurysm|Lens_luxation|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "Marfan_syndrome|not_specified|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Weill-Marchesani_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_specified|Acromicric_dysplasia": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cardiovascular_phenotype|Marfan_syndrome": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|not_provided|not_specified|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Connective_tissue_disorder": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Isolated_thoracic_aortic_aneurysm|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Connective_tissue_disorder|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified|not_provided": 1,
    "Acromicric_dysplasia|FBN1-related_disorder|Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thoracic_aortic_aneurysm_or_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Marfan_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|not_provided|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_specified": 1,
    "Marfan_syndrome|not_provided|Familial_aortopathy": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|Marfan_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia": 1,
    "Connective_tissue_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|MASS_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Marfan_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant": 2,
    "Marfan_syndrome|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|not_provided|not_specified": 1,
    "Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Acromicric_dysplasia|not_provided|MASS_syndrome": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Hirschsprung_disease|_susceptibility_to|_1|not_provided": 1,
    "Thoracic_aortic_aneurysm_or_dissection|not_provided": 2,
    "not_provided|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Lens_subluxation|Tall_stature|Myopia|Pectus_carinatum": 1,
    "not_provided|Vascular_dilatation": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Ectopia_lentis|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|MASS_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|Marfan_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|MARFAN_SYNDROME|_AUTOSOMAL_RECESSIVE": 1,
    "Marfan_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Marfan_syndrome|Left_ventricular_diastolic_dysfunction": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "not_specified|not_provided|Marfan_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Stiff_skin_syndrome|not_specified": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|not_specified|Weill-Marchesani_syndrome|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "FBN1-related_disorder|not_specified": 1,
    "Geleophysic_dysplasia_2|Marfan_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|Marfan_syndrome|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Weill-Marchesani_syndrome|Geleophysic_dysplasia": 1,
    "not_provided|FBN1-related_disorder|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided": 1,
    "Marfan_syndrome|Achondroplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Isolated_thoracic_aortic_aneurysm|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome": 1,
    "not_specified|not_provided|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Connective_tissue_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm|Marfan_syndrome|not_provided|Stiff_skin_syndrome": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|Marfan_syndrome": 1,
    "MASS_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Marfan_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Stiff_skin_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|not_provided|not_specified": 1,
    "Acromicric_dysplasia|Geleophysic_dysplasia|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia": 1,
    "Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Myopia|Tall_stature|Pectus_excavatum|Joint_hypermobility|Inguinal_hernia": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Craniosynostosis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|not_provided|not_specified|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "FBN1-related_disorder|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Weill-Marchesani_syndrome|Geleophysic_dysplasia": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|not_provided|Familial_ectopia_lentis": 1,
    "Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Stiff_skin_syndrome|Marfan_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Primary_dilated_cardiomyopathy": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|not_provided": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome_2|_dominant|not_provided": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Marfan_syndrome|not_provided": 1,
    "Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Weill-Marchesani_syndrome|not_specified|Connective_tissue_disorder|Acromicric_dysplasia|not_provided|Stiff_skin_syndrome": 1,
    "Marfan_syndrome|not_provided|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Isolated_thoracic_aortic_aneurysm": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis|Mitral_regurgitation|Aortic_dissection": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|Marfan_syndrome|Acromicric_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia": 1,
    "Stiff_skin_syndrome|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FBN1-related_disorder|Acromicric_dysplasia|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Acromicric_dysplasia|Marfan_syndrome|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|Connective_tissue_disorder|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia": 1,
    "Marfan_syndrome|Marfan_Syndrome/Loeys-Dietz_Syndrome/Familial_Thoracic_Aortic_Aneurysms_and_Dissections|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Stiff_skin_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Weill-Marchesani_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant": 1,
    "Marfan_syndrome|FBN1-related_disorder|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FBN1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|not_specified": 1,
    "Acromicric_dysplasia|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Marfan_syndrome|_atypical|Aortic_dissection|Lens_subluxation|Arachnodactyly|High_palate": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome|not_provided": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|FBN1-related_disorder": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2": 1,
    "MASS_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Stiff_skin_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Connective_tissue_disorder|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Marfan_syndrome|MASS_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_provided|Stiff_skin_syndrome|See_cases|FBN1-related_disorder": 1,
    "Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Geleophysic_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Acromicric_dysplasia": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Stiff_skin_syndrome|Weill-Marchesani_syndrome_2|_dominant|Geleophysic_dysplasia_2|MASS_syndrome": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia": 1,
    "Acute_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|not_provided": 1,
    "Familial_ectopia_lentis|Marfan_syndrome|MASS_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Geleophysic_dysplasia_2|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|MASS_syndrome|Acromicric_dysplasia|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|not_specified|MASS_syndrome|Stiff_skin_syndrome|Acromicric_dysplasia|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant|Ectopia_lentis_1|_isolated|_autosomal_dominant|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thoracic_aortic_aneurysm_or_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Geleophysic_dysplasia_2|Marfan_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|MASS_syndrome|Acromicric_dysplasia|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Acromicric_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|Weill-Marchesani_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_specified": 1,
    "Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|High|_narrow_palate|Dental_crowding|Arachnodactyly|Dolichocephaly|Joint_hypermobility|Aortic_regurgitation": 1,
    "Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia|Weill-Marchesani_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|MASS_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome|Acromicric_dysplasia|Stiff_skin_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia_2|Weill-Marchesani_syndrome_2|_dominant": 1,
    "Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|not_provided|Acromicric_dysplasia|not_specified|Geleophysic_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Weill-Marchesani_syndrome_2|_dominant|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|MASS_syndrome|Geleophysic_dysplasia_2|Stiff_skin_syndrome|Progeroid_and_marfanoid_aspect-lipodystrophy_syndrome": 1,
    "Stiff_skin_syndrome|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Acromicric_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Geleophysic_dysplasia": 1,
    "FBN1-related_disorder|Marfan_syndrome|not_provided|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Brugada_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Acromicric_dysplasia|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Geleophysic_dysplasia|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome": 1,
    "Stiff_skin_syndrome|Ectopia_lentis|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Weill-Marchesani_syndrome|Marfan_syndrome|Geleophysic_dysplasia|Acromicric_dysplasia|MASS_syndrome": 1,
    "Marfan_syndrome|Geleophysic_dysplasia|Stiff_skin_syndrome|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ectopia_lentis_1|_isolated|_autosomal_dominant|Acromicric_dysplasia": 1,
    "Geleophysic_dysplasia|Weill-Marchesani_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|not_specified": 1,
    "Stiff_skin_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Marfan_syndrome|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Weill-Marchesani_syndrome": 1,
    "Stiff_skin_syndrome|MASS_syndrome|Marfan_syndrome|Ectopia_lentis|Geleophysic_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Weill-Marchesani_syndrome": 2,
    "Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Marfan_syndrome|Geleophysic_dysplasia|not_provided|Acromicric_dysplasia|Weill-Marchesani_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Acromicric_dysplasia|Weill-Marchesani_syndrome|Marfan_syndrome|Ectopia_lentis_1|_isolated|_autosomal_dominant|Stiff_skin_syndrome": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 17,
    "Primary_Microcephaly|_Recessive|not_provided|Seckel_syndrome": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided": 14,
    "not_provided|Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive": 9,
    "Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive": 17,
    "CEP152-related_disorder|not_provided|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided|CEP152-related_disorder": 1,
    "not_provided|CEP152-related_disorder": 7,
    "Microcephaly_9|_primary|_autosomal_recessive": 23,
    "Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive|not_provided|not_specified": 1,
    "Seckel_syndrome_5|not_specified|Microcephaly_9|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 8,
    "Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided|not_specified|CEP152-related_disorder": 2,
    "CEP152-related_disorder|not_provided": 4,
    "Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive|not_provided|CEP152-related_disorder|not_specified": 1,
    "not_provided|not_specified|Seckel_syndrome_5": 1,
    "Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive|not_specified": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|CEP152-related_disorder|not_provided|Seckel_syndrome_5": 1,
    "Seckel_syndrome_5|not_specified|not_provided|Microcephaly_9|_primary|_autosomal_recessive": 3,
    "CEP152-related_disorder|not_specified|not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 1,
    "not_provided|not_specified|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 1,
    "not_provided|Seckel_syndrome_5": 2,
    "Inborn_genetic_diseases|not_provided|CEP152-related_disorder": 2,
    "CEP152-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|not_provided": 8,
    "Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided|not_specified": 3,
    "Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive|not_provided": 4,
    "Microcephaly_9|_primary|_autosomal_recessive|Inborn_genetic_diseases|Seckel_syndrome_5": 3,
    "CEP152-related_disorder": 6,
    "CEP152-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "not_specified|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided": 2,
    "Seckel_syndrome_5|not_provided|Microcephaly_9|_primary|_autosomal_recessive": 3,
    "not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_specified": 1,
    "CEP152-related_disorder|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided": 3,
    "Microcephaly_9|_primary|_autosomal_recessive|not_provided|Seckel_syndrome_5": 4,
    "not_specified|not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 1,
    "Seckel_syndrome_5|not_provided|not_specified|Microcephaly_9|_primary|_autosomal_recessive": 3,
    "CEP152-related_disorder|not_provided|not_specified|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 1,
    "not_provided|CEP152-related_disorder|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|not_provided|CEP152-related_disorder": 1,
    "CEP152-related_disorder|Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive|not_provided": 1,
    "not_provided|CEP152-related_disorder|Inborn_genetic_diseases": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Microcephaly_9|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly_9|_primary|_autosomal_recessive": 4,
    "Inborn_genetic_diseases|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive|not_provided|CEP152-related_disorder": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_specified|not_provided": 2,
    "Seckel_syndrome_5|not_provided": 1,
    "not_specified|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided|CEP152-related_disorder": 1,
    "Inborn_genetic_diseases|Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "not_specified|not_provided|Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|not_provided|not_specified": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "CEP152-related_disorder|Inborn_genetic_diseases|not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5": 1,
    "not_provided|Seckel_syndrome_5|not_specified": 1,
    "not_specified|not_provided|CEP152-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "Seckel_syndrome_5|not_provided|CEP152-related_disorder|Microcephaly_9|_primary|_autosomal_recessive|not_specified": 1,
    "not_specified|Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "CEP152-related_disorder|not_specified|Seckel_syndrome_5|not_provided|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "CEP152-related_disorder|Inborn_genetic_diseases|Seckel_syndrome_5|not_specified|not_provided|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Microcephaly_9|_primary|_autosomal_recessive|not_provided|Seckel_syndrome_5": 1,
    "not_specified|CEP152-related_disorder|Inborn_genetic_diseases|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome_5|not_provided": 3,
    "Seckel_syndrome_5|not_provided|Microcephaly_9|_primary|_autosomal_recessive|not_specified": 1,
    "not_provided|Microcephaly_9|_primary|_autosomal_recessive|CEP152-related_disorder|Seckel_syndrome_5": 1,
    "Microcephaly_9|_primary|_autosomal_recessive|Inborn_genetic_diseases|not_provided|Seckel_syndrome_5": 2,
    "CEP152-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "CEP152-related_disorder|not_specified|not_provided|Seckel_syndrome_5|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "not_provided|Microcephaly_9|_primary|_autosomal_recessive|Seckel_syndrome": 1,
    "not_provided|Seckel_syndrome_5|not_specified|Microcephaly_9|_primary|_autosomal_recessive": 1,
    "HDC-related_disorder": 3,
    "not_specified|HDC-related_disorder": 1,
    "HDC-related_disorder|not_provided": 1,
    "not_provided|HDC-related_disorder": 1,
    "USP8-related_disorder|Hereditary_spastic_paraplegia": 2,
    "USP8-related_disorder": 2,
    "not_provided|Hereditary_spastic_paraplegia|USP8-related_disorder": 3,
    "Autosomal_recessive_spastic_paraplegia_type_59|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Pituitary_dependent_hypercortisolism": 1,
    "not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_provided|TRPM7-related_disorder": 4,
    "TRPM7-related_disorder": 7,
    "Amyotrophic_lateral_sclerosis-parkinsonism-dementia_complex|not_specified": 2,
    "Juvenile_amyotrophic_lateral_sclerosis|TRPM7-related_disorder|not_provided|.": 1,
    "TRPM7-related_disorder|not_provided": 2,
    "TRPM7-associated_neuropathological_disorder": 1,
    "Amyotrophic_lateral_sclerosis-parkinsonism-dementia_complex|TRPM7-related_disorder|not_provided": 1,
    "SPPL2A-related_disorder": 1,
    "Immunodeficiency_86": 2,
    "not_specified|AP4E1-related_disorder": 1,
    "AP4E1-related_disorder|Spastic_paraplegia|not_specified": 1,
    "Spastic_paraplegia|AP-4_deficiency_syndrome": 1,
    "Hereditary_spastic_paraplegia_51|not_provided|Stuttering|_familial_persistent|_1": 3,
    "not_provided|AP4E1-related_disorder|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_51|Stuttering|_familial_persistent|_1|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_51": 1,
    "Spastic_paraplegia|Congenital_myopathy|not_provided": 1,
    "Hereditary_spastic_paraplegia_51": 9,
    "Hereditary_spastic_paraplegia_51|Stuttering|_familial_persistent|_1|not_provided": 2,
    "Spastic_paraplegia|Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51": 1,
    "Spastic_paraplegia|AP4E1-related_disorder": 3,
    "Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia_51": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_51": 2,
    "Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_51|not_provided": 1,
    "Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Stuttering|_familial_persistent|_1": 1,
    "AP4E1-related_disorder|not_specified|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_51|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|AP4E1-related_disorder|Spastic_paraplegia": 1,
    "AP-4_deficiency_syndrome|Spastic_paraplegia|not_provided": 1,
    "not_provided|not_specified|Spastic_paraplegia|Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_51": 1,
    "AP4E1-related_disorder": 3,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "AP-4_deficiency_syndrome|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_51|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|Stuttering|_familial_persistent|_1|not_provided": 1,
    "Hereditary_spastic_paraplegia|Spastic_paraplegia|not_provided|not_specified|AP4E1-related_disorder": 1,
    "Hereditary_spastic_paraplegia|AP4E1-related_disorder|not_provided|Spastic_paraplegia|Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|not_specified": 1,
    "AP4E1-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|not_specified": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|not_provided|Neurodevelopmental_delay": 1,
    "not_provided|Hereditary_spastic_paraplegia_51|Spastic_paraplegia": 1,
    "AP4E1-related_disorder|Spastic_paraplegia": 1,
    "Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|not_provided": 2,
    "Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|Spastic_paraplegia": 1,
    "AP4E1-related_disorder|Spastic_paraplegia|not_provided": 1,
    "Stuttering|_familial_persistent|_1": 1,
    "Stuttering|_familial_persistent|_1|not_specified|Hereditary_spastic_paraplegia_51|Spastic_paraplegia": 1,
    "AP4E1-related_disorder|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|Stuttering|_familial_persistent|_1|not_provided|AP4E1-related_disorder|not_specified|Hereditary_spastic_paraplegia_51": 1,
    "Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|AP4E1-related_disorder|Spastic_paraplegia|not_provided|Stuttering|_familial_persistent|_1|Hereditary_spastic_paraplegia_51|not_specified": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|Stuttering|_familial_persistent|_1": 1,
    "not_specified|Stuttering|_familial_persistent|_1|Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_51": 1,
    "Spastic_paraplegia|not_specified|not_provided|AP4E1-related_disorder|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Stuttering|_familial_persistent|_1|not_specified|Hereditary_spastic_paraplegia_51": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_51|Stuttering|_familial_persistent|_1|Spastic_paraplegia|not_specified": 1,
    "Stuttering|Spastic_paraplegia": 1,
    "Peripheral_neuropathy|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_51|ALG12-congenital_disorder_of_glycosylation|Spastic_paraplegia": 1,
    "Spastic_paraplegia|AP4E1-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_51|not_specified|not_provided|Spastic_paraplegia": 1,
    "Aromatase_deficiency": 106,
    "not_provided|Aromatase_deficiency": 33,
    "Aromatase_deficiency|not_provided": 15,
    "Letrozole_response|not_specified|not_provided|Aromatase_excess_syndrome|Aromatase_deficiency": 1,
    "Aromatase_deficiency|Aromatase_excess_syndrome": 5,
    "Aromatase_excess_syndrome|not_provided": 1,
    "Aromatase_deficiency|not_provided|Aromatase_excess_syndrome": 2,
    "not_provided|Aromatase_excess_syndrome|Aromatase_deficiency": 1,
    "Aromatase_excess_syndrome|Aromatase_deficiency|not_provided": 1,
    "not_provided|CYP19A1-related_disorder|Aromatase_deficiency": 2,
    "not_provided|Aromatase_deficiency|Aromatase_excess_syndrome": 3,
    "not_specified|Aromatase_deficiency": 1,
    "not_provided|not_specified|Aromatase_deficiency": 1,
    "not_specified|not_provided|Aromatase_deficiency": 2,
    "Premature_ovarian_failure|Aromatase_deficiency": 1,
    "Aromatase_excess_syndrome|Aromatase_deficiency": 1,
    "CYP19A1-related_disorder|not_provided": 1,
    "Aromatase_excess_syndrome|Aromatase_deficiency|not_specified": 1,
    "not_specified|not_provided|Aromatase_deficiency|Aromatase_excess_syndrome": 1,
    "not_provided|Aromatase_deficiency|CYP19A1-related_disorder": 1,
    "CYP19A1-related_disorder|Aromatase_deficiency|not_provided": 1,
    "Lethal_congenital_contracture_syndrome_11": 19,
    "Lethal_congenital_contracture_syndrome_11|not_provided": 3,
    "Aromatase_deficiency|Lethal_congenital_contracture_syndrome_11|not_provided": 1,
    "GLDN-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Lethal_congenital_contracture_syndrome_11": 3,
    "GLDN-related_disorder": 15,
    "GLDN-related_disorder|Lethal_congenital_contracture_syndrome_11|not_provided": 1,
    "Polyhydramnios|Multiple_joint_contractures": 1,
    "Lethal_congenital_contracture_syndrome_11|Inborn_genetic_diseases": 1,
    "Lethal_congenital_contracture_syndrome_11|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "Polyhydramnios|Multiple_joint_contractures|Lethal_congenital_contracture_syndrome_11": 1,
    "Inborn_genetic_diseases|Lethal_congenital_contracture_syndrome_11|Breathing_dysregulation|Congenital_contracture|Polyhydramnios|Flexion_contracture": 1,
    "Lethal_congenital_contracture_syndrome_11|not_provided|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|GLDN-related_disorder": 1,
    "DMXL2-related_disorder|not_specified": 1,
    "not_provided|DMXL2-related_disorder": 20,
    "Polyendocrine-polyneuropathy_syndrome": 1,
    "DMXL2-related_disorder|not_provided": 22,
    "Hearing_loss|_autosomal_dominant_71": 5,
    "DMXL2-related_disorder": 12,
    "Hearing_loss|_autosomal_dominant_71|Inborn_genetic_diseases|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_71|not_provided": 3,
    "Polyendocrine-polyneuropathy_syndrome|Developmental_and_epileptic_encephalopathy|_81|Hearing_loss|_autosomal_dominant_71|not_provided": 2,
    "DMXL2-related_disorder|Developmental_and_epileptic_encephalopathy|_81|Hearing_loss|_autosomal_dominant_71|Polyendocrine-polyneuropathy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Polyendocrine-polyneuropathy_syndrome": 1,
    "Hearing_loss|_autosomal_dominant_71|Developmental_and_epileptic_encephalopathy|_81|Polyendocrine-polyneuropathy_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_81": 12,
    "Hearing_loss|_autosomal_dominant_71|Polyendocrine-polyneuropathy_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_81": 1,
    "Developmental_and_epileptic_encephalopathy|_81|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_71": 2,
    "Developmental_and_epileptic_encephalopathy|_81|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|DMXL2-related_disorder": 4,
    "Inborn_genetic_diseases|DMXL2-related_disorder|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_71|not_provided|Polyendocrine-polyneuropathy_syndrome|Developmental_and_epileptic_encephalopathy|_81": 1,
    "DMXL2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_71|Developmental_and_epileptic_encephalopathy|_81|Polyendocrine-polyneuropathy_syndrome|Inborn_genetic_diseases|DMXL2-related_disorder": 1,
    "See_cases|not_provided|Polyendocrine-polyneuropathy_syndrome": 1,
    "not_provided|Polyendocrine-polyneuropathy_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_81|Polyendocrine-polyneuropathy_syndrome|Hearing_loss|_autosomal_dominant_71": 1,
    "Inborn_genetic_diseases|DMXL2-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_81|Hearing_loss|_autosomal_dominant_71|not_provided|Polyendocrine-polyneuropathy_syndrome": 3,
    "not_provided|Spasticity|Polyendocrine-polyneuropathy_syndrome": 1,
    "DMXL2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "DMXL2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Nonsyndromic_genetic_hearing_loss|not_provided|DMXL2-related_disorder": 1,
    "not_provided|DMXL2-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|DMXL2-related_disorder|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_71|Developmental_and_epileptic_encephalopathy|_81|Polyendocrine-polyneuropathy_syndrome": 1,
    "Polyendocrine-polyneuropathy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Polyendocrine-polyneuropathy_syndrome|Hearing_loss|_autosomal_dominant_71|Developmental_and_epileptic_encephalopathy|_81": 1,
    "Developmental_and_epileptic_encephalopathy|_81|Hearing_loss|_autosomal_dominant_71|Polyendocrine-polyneuropathy_syndrome|not_provided": 1,
    "DMXL2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_81": 1,
    "Polyendocrine-polyneuropathy_syndrome|not_provided|Inborn_genetic_diseases|DMXL2-related_disorder": 2,
    "Nonsyndromic_genetic_hearing_loss|not_provided|Amenorrhea": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_81|Hearing_loss|_autosomal_dominant_71|Polyendocrine-polyneuropathy_syndrome": 1,
    "Nonsyndromic_genetic_hearing_loss|Inborn_genetic_diseases|DMXL2-related_disorder|Polyendocrine-polyneuropathy_syndrome|Hearing_loss|_autosomal_dominant_71|Developmental_and_epileptic_encephalopathy|_81|not_provided": 1,
    "Inborn_genetic_diseases|Nonsyndromic_genetic_hearing_loss|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_81|not_provided|Hearing_loss|_autosomal_dominant_71|Polyendocrine-polyneuropathy_syndrome": 1,
    "not_provided|Polyendocrine-polyneuropathy_syndrome|Developmental_and_epileptic_encephalopathy|_81|Hearing_loss|_autosomal_dominant_71": 1,
    "Hearing_loss|_autosomal_dominant_71|Polyendocrine-polyneuropathy_syndrome|Developmental_and_epileptic_encephalopathy|_81|not_provided": 1,
    "LEO1-related_disorder": 12,
    "not_specified|LEO1-related_disorder": 1,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome": 14,
    "not_provided|Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|Inborn_genetic_diseases": 1,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome": 1,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|Language_delay_and_attention_deficit-hyperactivity_disorder/cognitive_impairment_with_or_without_cardiac_arrhythmia|not_provided": 1,
    "Language_delay_and_attention_deficit-hyperactivity_disorder/cognitive_impairment_with_or_without_cardiac_arrhythmia": 1,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|Language_delay_and_attention_deficit-hyperactivity_disorder/cognitive_impairment_with_or_without_cardiac_arrhythmia": 2,
    "GNB5-related_disorder": 3,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|Inborn_genetic_diseases": 2,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|Language_delay_and_attention_deficit-hyperactivity_disorder/cognitive_impairment_with_or_without_cardiac_arrhythmia|Inborn_genetic_diseases|not_provided|Global_developmental_delay|Delayed_speech_and_language_development|Attention_deficit_hyperactivity_disorder": 1,
    "Global_developmental_delay|Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome": 1,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|Language_delay_and_attention_deficit-hyperactivity_disorder/cognitive_impairment_with_or_without_cardiac_arrhythmia|LODDER-MERLA_SYNDROME|_TYPE_2|_WITH_DEVELOPMENTAL_DELAY_AND_CARDIAC_ARRHYTHMIA|not_provided": 1,
    "Gnb5-related_intellectual_disability-cardiac_arrhythmia_syndrome|GNB5-reled_disorder|GNB5-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|GNB5-related_disorder|not_specified": 1,
    "MYO5A-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Griscelli_syndrome_type_1": 1,
    "not_provided|MYO5A-related_disorder": 10,
    "Griscelli_syndrome_type_1": 15,
    "not_provided|Griscelli_syndrome_type_1": 4,
    "MYO5A-related_disorder": 9,
    "Griscelli_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Griscelli_syndrome_type_1|not_provided": 5,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided|MYO5A-related_disorder": 1,
    "Cerebellar_cortical_atrophy|Dystonic_disorder|Seizure|Global_developmental_delay|Nystagmus": 1,
    "Griscelli_syndrome_type_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Griscelli_syndrome_type_1": 3,
    "not_provided|Inborn_genetic_diseases|MYO5A-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|not_provided|Griscelli_syndrome_type_1": 1,
    "not_provided|MYO5A-related_disorder|Congenital_heart_disease": 1,
    "not_provided|Griscelli_syndrome_type_1|MYO5A-related_disorder": 1,
    "not_provided|not_specified|Griscelli_syndrome_type_1": 1,
    "not_provided|Griscelli_syndrome_type_1|not_specified": 1,
    "not_provided|Amelogenesis_Imperfecta|_Recessive": 16,
    "not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A3": 5,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3": 239,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3|Inborn_genetic_diseases": 28,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3|Amelogenesis_Imperfecta|_Recessive": 1,
    "not_provided|WDR72-related_disorder|Amelogenesis_Imperfecta|_Recessive": 2,
    "WDR72-related_disorder": 5,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3|not_provided": 4,
    "Inborn_genetic_diseases|Amelogenesis_imperfecta_hypomaturation_type_2A3": 11,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3|WDR72-related_disorder": 1,
    "Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Amelogenesis_imperfecta_hypomaturation_type_2A3": 2,
    "Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 4,
    "not_specified|Amelogenesis_imperfecta_hypomaturation_type_2A3|Amelogenesis_Imperfecta|_Recessive|not_provided": 4,
    "WDR72-related_disorder|Amelogenesis_imperfecta_hypomaturation_type_2A3": 2,
    "Inborn_genetic_diseases|WDR72-related_disorder|not_provided": 1,
    "Amelogenesis_imperfecta|Amelogenesis_imperfecta_hypomaturation_type_2A3": 1,
    "Amelogenesis_Imperfecta|_Recessive|not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A3": 1,
    "not_specified|not_provided|Amelogenesis_imperfecta_hypomaturation_type_2A3|Amelogenesis_Imperfecta|_Recessive": 1,
    "Distal_renal_tubular_acidosis|Hypophosphatemic_rickets": 1,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3|WDR72-related_disorder|not_provided": 1,
    "Amelogenesis_Imperfecta|_Recessive|Amelogenesis_imperfecta_hypomaturation_type_2A3|not_provided|not_specified": 1,
    "Amelogenesis_imperfecta_hypomaturation_type_2A3|not_provided|Amelogenesis_imperfecta": 1,
    "Clubfoot|Abnormal_finger_morphology|Cystic_renal_dysplasia|Abnormality_of_the_face|Renal_cyst": 1,
    "Griscelli_syndrome|not_provided": 1,
    "Griscelli_syndrome_type_2|not_provided": 6,
    "Griscelli_syndrome_type_2": 213,
    "Griscelli_syndrome": 5,
    "not_provided|Griscelli_syndrome_type_2": 15,
    "not_specified|not_provided|Griscelli_syndrome_type_2": 2,
    "Griscelli_syndrome_type_2|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Griscelli_syndrome_type_2": 7,
    "Autoinflammatory_syndrome|not_provided|Griscelli_syndrome_type_2|not_specified": 1,
    "RAB27A-related_disorder": 1,
    "not_specified|not_provided|Griscelli_syndrome_type_2|RAB27A-related_disorder|Autoinflammatory_syndrome": 1,
    "Griscelli_syndrome_type_2|Autoinflammatory_syndrome": 10,
    "Griscelli_syndrome_type_2|not_provided|Autoinflammatory_syndrome": 1,
    "Griscelli_syndrome_type_2|Autoinflammatory_syndrome|not_provided": 1,
    "RAB27A-related_disorder|Griscelli_syndrome_type_2|not_provided": 1,
    "Griscelli_syndrome_type_2|not_specified|RAB27A-related_disorder": 1,
    "Autoinflammatory_syndrome|Griscelli_syndrome_type_2": 7,
    "See_cases|Griscelli_syndrome_type_2": 1,
    "RAB27A-related_disorder|Griscelli_syndrome_type_2": 1,
    "Autoinflammatory_syndrome|not_provided|Griscelli_syndrome_type_2": 1,
    "Multisystem_inflammatory_syndrome_in_children|Griscelli_syndrome_type_2|See_cases": 1,
    "Griscelli_syndrome_type_2|RAB27A-related_disorder": 3,
    "Griscelli_syndrome_type_2|Griscelli_syndrome": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|Griscelli_syndrome_type_2": 1,
    "Autoinflammatory_syndrome|Griscelli_syndrome_type_2|RAB27A-related_disorder|not_provided": 1,
    "not_provided|Griscelli_syndrome_type_2|Inborn_genetic_diseases|Autoinflammatory_syndrome": 1,
    "Griscelli_syndrome|Griscelli_syndrome_type_2": 1,
    "not_specified|Griscelli_syndrome_type_2": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_80": 4,
    "Developmental_and_epileptic_encephalopathy|_80|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|PIGB-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_80": 11,
    "PIGB-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_80|not_provided|PIGB-related_disorder": 1,
    "not_provided|PIGB-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy|_80|Hyperphosphatasia_with_intellectual_disability_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_80": 1,
    "Primary_ciliary_dyskinesia_25|not_provided|Dyslexia|_susceptibility_to|_1|not_specified": 1,
    "Primary_ciliary_dyskinesia_25|Inborn_genetic_diseases|Dyslexia|_susceptibility_to|_1|not_provided": 1,
    "DNAAF4-related_disorder": 3,
    "not_provided|Dyslexia|_susceptibility_to|_1": 2,
    "not_provided|DNAAF4-related_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_25": 1,
    "Primary_ciliary_dyskinesia_25|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_25": 4,
    "not_provided|DNAAF4-related_disorder|Inborn_genetic_diseases": 1,
    "DNAAF4-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_25": 1,
    "Primary_ciliary_dyskinesia_25|Dyslexia|_susceptibility_to|_1|not_provided": 1,
    "Primary_ciliary_dyskinesia_25|Inborn_genetic_diseases|not_provided": 1,
    "Primary_ciliary_dyskinesia_25|not_provided": 5,
    "Dyslexia|_susceptibility_to|_1|Primary_ciliary_dyskinesia_25|not_provided": 1,
    "not_provided|Dyslexia|_susceptibility_to|_1|Primary_ciliary_dyskinesia_25": 2,
    "Primary_ciliary_dyskinesia_25|not_provided|not_specified": 1,
    "Primary_ciliary_dyskinesia_25|DNAAF4-related_disorder|not_provided": 1,
    "Primary_ciliary_dyskinesia_25|not_provided|Primary_ciliary_dyskinesia|Dyslexia|_susceptibility_to|_1": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_25": 1,
    "Dyslexia|_susceptibility_to|_1|Primary_ciliary_dyskinesia_25": 1,
    "Dyslexia|_susceptibility_to|_1|Primary_ciliary_dyskinesia_25|not_provided|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia|Dyslexia|_susceptibility_to|_1|Primary_ciliary_dyskinesia_25|not_provided": 1,
    "Dyslexia|_susceptibility_to|_1": 1,
    "not_specified|Dyslexia|_susceptibility_to|_1|not_provided": 1,
    "NEDD4-related_disorder": 2,
    "NEDD4-related_disorder|not_provided": 1,
    "RFX7-related_disorder": 7,
    "RFX7-related_disorder|not_provided": 4,
    "Intellectual_developmental_disorder|_autosomal_dominant_71|_with_behavioral_abnormalities": 16,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_71|_with_behavioral_abnormalities": 3,
    "Intellectual_developmental_disorder|_autosomal_dominant_71|_with_behavioral_abnormalities|not_provided|See_cases": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_71|_with_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "not_provided|RFX7-related_disorder": 1,
    "Inborn_genetic_diseases|RFX7-related_disorder": 1,
    "MNS1-related_disorder|not_provided": 1,
    "Heterotaxy|_visceral|_9|_autosomal|_with_male_infertility": 9,
    "MNS1-related_disorder": 3,
    "MNS1-related_disorder|Heterotaxy|_visceral|_9|_autosomal|_with_male_infertility|not_provided": 1,
    "Situs_inversus|MNS1-related_disorder|Heterotaxy|_visceral|_9|_autosomal|_with_male_infertility": 1,
    "TCF12-related_craniosynostosis": 31,
    "Hypogonadotropic_hypogonadism_26_with_or_without_anosmia": 2,
    "TCF12-related_disorder": 12,
    "TCF12-related_craniosynostosis|not_provided": 12,
    "TCF12-related_craniosynostosis|Hypogonadotropic_hypogonadism_26_with_or_without_anosmia": 3,
    "not_provided|TCF12-related_disorder": 5,
    "HYPOGONADOTROPIC_HYPOGONADISM_26_WITH_ANOSMIA": 4,
    "Hypogonadotropic_hypogonadism_26_with_or_without_anosmia|TCF12-related_craniosynostosis": 3,
    "not_provided|TCF12-related_craniosynostosis": 3,
    "TCF12-related_disorder|Inborn_genetic_diseases": 1,
    "Autism_spectrum_disorder|not_provided|Hypogonadotropic_hypogonadism_26_with_or_without_anosmia": 1,
    "Coronal_craniosynostosis": 1,
    "Hypogonadotropic_hypogonadism_26_with_or_without_anosmia|not_provided": 1,
    "HYPOGONADOTROPIC_HYPOGONADISM_26_WITH_ANOSMIA|TCF12-related_craniosynostosis|not_provided": 1,
    "not_provided|Autism_spectrum_disorder|TCF12-related_craniosynostosis": 1,
    "not_provided|Hypogonadotropic_hypogonadism_26_with_or_without_anosmia|TCF12-related_craniosynostosis": 1,
    "TCF12-related_craniosynostosis|not_provided|TCF12-related_disorder": 1,
    "not_provided|Hypogonadotropic_hypogonadism_26_with_or_without_anosmia|TCF12-related_craniosynostosis|not_specified": 1,
    "CGNL1-related_disorder": 21,
    "not_specified|not_provided|CGNL1-related_disorder": 1,
    "CGNL1-related_disorder|not_specified": 1,
    "Cardiomyopathy|_dilated|_2K|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_2K": 4,
    "not_provided|ALDH1A2-related_disorder": 2,
    "Diaphragmatic_hernia_4|_with_cardiovascular_defects": 7,
    "ALDH1A2-related_disorder|not_provided": 2,
    "ALDH1A2-related_disorder": 4,
    "not_specified|not_provided|ALDH1A2-related_disorder": 1,
    "High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12": 2,
    "not_provided|Diabetes_mellitus_type_2|_susceptibility_to|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12": 1,
    "not_provided|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency": 13,
    "Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency": 19,
    "not_provided|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus": 1,
    "High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus|not_specified|not_provided": 1,
    "Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|not_provided": 14,
    "not_provided|LIPC-related_disorder|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency": 1,
    "High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus": 4,
    "Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|not_specified|not_provided": 6,
    "not_specified|not_provided|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12": 1,
    "LIPC-related_disorder": 2,
    "not_provided|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus": 1,
    "Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|not_provided|Type_2_diabetes_mellitus": 1,
    "LIPC-related_disorder|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|not_provided": 2,
    "LIPC-related_disorder|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|not_provided|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12|Type_2_diabetes_mellitus": 1,
    "Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus": 1,
    "Type_2_diabetes_mellitus|Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_1_diabetes_mellitus_2|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_12|not_specified|not_provided": 1,
    "Hyperlipidemia_due_to_hepatic_triglyceride_lipase_deficiency|Type_2_diabetes_mellitus|LIPC-related_disorder|not_provided": 1,
    "ADAM10-related_disorder": 7,
    "Reticulate_acropigmentation_of_Kitamura": 7,
    "Alzheimer_disease_18": 1,
    "not_specified|not_provided|Alzheimer_disease_18": 1,
    "not_provided|Corticobasal_syndrome": 1,
    "not_provided|Reticulate_acropigmentation_of_Kitamura|Alzheimer_disease_18": 1,
    "Focal_segmental_glomerulosclerosis_6": 105,
    "MYO1E-related_disorder": 8,
    "not_provided|Focal_segmental_glomerulosclerosis_6": 35,
    "Focal_segmental_glomerulosclerosis_6|not_provided": 20,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_6": 4,
    "Focal_segmental_glomerulosclerosis_6|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_6": 5,
    "not_provided|Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_6": 2,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_6|not_provided": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_6|MYO1E-related_disorder": 3,
    "Focal_segmental_glomerulosclerosis_6|MYO1E-related_disorder|not_provided": 2,
    "Focal_segmental_glomerulosclerosis_6|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Focal_segmental_glomerulosclerosis_6|Inborn_genetic_diseases": 3,
    "not_provided|MYO1E-related_disorder": 6,
    "not_specified|Focal_segmental_glomerulosclerosis_6": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_6": 2,
    "Focal_segmental_glomerulosclerosis_6|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|MYO1E-related_disorder|Focal_segmental_glomerulosclerosis_6": 1,
    "not_provided|MYO1E-related_disorder|Inborn_genetic_diseases": 1,
    "MYO1E-related_disorder|not_provided": 3,
    "Microscopic_hematuria|not_specified|not_provided|Kidney_disorder": 1,
    "MYO1E-related_disorder|Focal_segmental_glomerulosclerosis_6": 1,
    "Nephrotic_syndrome|Focal_segmental_glomerulosclerosis_6": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_6": 2,
    "Focal_segmental_glomerulosclerosis_6|MYO1E-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_6|not_specified|MYO1E-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Focal_segmental_glomerulosclerosis_6": 1,
    "Focal_segmental_glomerulosclerosis_6|not_provided|MYO1E-related_disorder": 1,
    "MYO1E-related_disorder|not_specified|not_provided|Focal_segmental_glomerulosclerosis_6": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_6|Kidney_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_6|not_specified": 1,
    "MYO1E-related_disorder|not_specified|not_provided": 1,
    "ICE2-related_disorder": 11,
    "NARG2-related_Intellectual_disability": 2,
    "not_provided|ICE2-related_disorder": 1,
    "Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia": 52,
    "not_provided|Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia": 5,
    "RORA-related_disorder|not_provided": 5,
    "Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia|not_provided": 4,
    "Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia|Severe_intellectual_deficiency": 1,
    "RORA-related_disorder": 5,
    "See_cases|Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia": 1,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia|not_provided|See_cases": 1,
    "Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia|Inborn_genetic_diseases": 2,
    "not_specified|Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_or_without_epilepsy_or_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|not_provided|VPS13C-related_disorder": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_23|not_provided": 14,
    "VPS13C-related_disorder|not_provided": 19,
    "VPS13C-related_disorder": 20,
    "not_provided|VPS13C-related_disorder": 20,
    "not_provided|Autosomal_recessive_early-onset_Parkinson_disease_23": 4,
    "Parkinson_disease|Autosomal_recessive_early-onset_Parkinson_disease_23": 3,
    "not_specified|not_provided|VPS13C-related_disorder": 2,
    "Parkinson_disease|Young-onset_Parkinson_disease|not_provided|Autosomal_recessive_early-onset_Parkinson_disease_23": 1,
    "VPS13C-related_disorder|Young-onset_Parkinson_disease": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_23|Young-onset_Parkinson_disease": 1,
    "Autosomal_recessive_early-onset_Parkinson_disease_23|not_provided|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y": 3,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y": 7,
    "Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 2,
    "Cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1Y": 12,
    "Left_ventricular_noncompaction_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Dilated_cardiomyopathy_1Y|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|See_cases|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_21|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_3": 11,
    "TPM1-related_disorder|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|TPM1-related_disorder|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_3|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Cardiomyopathy": 1,
    "not_specified|TPM1-related_disorder|Cardiomyopathy|not_provided": 1,
    "not_provided|TPM1-related_disorder|not_specified": 1,
    "Cardiomyopathy|TPM1-related_disorder|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Cardiomyopathy": 3,
    "Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1Y|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 2,
    "Long_QT_syndrome|Paroxysmal_familial_ventricular_fibrillation|not_specified": 1,
    "TPM1-related_disorder": 2,
    "Dilated_cardiomyopathy_1Y|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_1Y": 2,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1Y|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_3": 2,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_9|not_provided|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1Y|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "TPM1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_specified": 1,
    "Pulmonary_atresia_with_intact_ventricular_septum": 1,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "TPM1-related_disorder|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Effort-induced_polymorphic_ventricular_tachycardia": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "TPM1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Familial_cardiomyopathy|Left_ventricular_noncompaction_9|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1Y|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Hypertrophic_cardiomyopathy_3|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y": 1,
    "TPM1-related_disorder|not_provided|Cardiomyopathy": 1,
    "TPM1-related_disorder|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y": 1,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 2,
    "Cardiovascular_phenotype|Left_ventricular_noncompaction_9|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_3|Primary_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_3|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y": 1,
    "not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1Y|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "TPM1-related_disorder|not_provided|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1Y": 1,
    "not_provided|TPM1-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Left_ventricular_noncompaction_9|not_provided": 1,
    "not_provided|not_specified|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3": 2,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_3|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Left_ventricular_noncompaction": 1,
    "Hypertrophic_cardiomyopathy_3|not_specified": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_1": 10,
    "TPM1-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy_3|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1Y": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1Y|TPM1-related_disorder|not_provided|Hypertrophic_cardiomyopathy_3": 1,
    "not_specified|TPM1-related_disorder|not_provided|Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y": 1,
    "Hypertrophic_cardiomyopathy_3|Dilated_cardiomyopathy_1Y|not_provided": 2,
    "TPM1-related_disorder|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|TPM1-related_disorder": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Isolated_hyperchlorhidrosis": 8,
    "CA12-related_disorder": 3,
    "not_provided|Isolated_hyperchlorhidrosis": 2,
    "CA12-related_disorder|not_provided": 1,
    "not_provided|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Inborn_genetic_diseases": 1,
    "HERC1-related_disorder|not_provided": 15,
    "HERC1-related_disorder": 10,
    "HERC1-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|not_provided": 1,
    "not_provided|HERC1-related_disorder": 13,
    "not_provided|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation": 6,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|not_provided": 16,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|HERC1-related_disorder": 2,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Megalencephaly_with_thick_corpus_callosum|_cerebellar_atrophy|_and_intellectual_disability": 2,
    "not_specified|HERC1-related_disorder|not_provided": 2,
    "HERC1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|not_provided|HERC1-related_disorder": 1,
    "not_provided|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Inborn_genetic_diseases|not_specified": 1,
    "HERC1-related_disorder|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|not_provided": 1,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Inborn_genetic_diseases|HERC1-related_disorder": 1,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Inborn_genetic_diseases|HERC1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation": 2,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|HERC1-related_disorder|not_provided": 2,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|HERC1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "HERC1-related_disorder|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation|HERC1-related_disorder": 1,
    "not_provided|not_specified|HERC1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Macrocephaly|_dysmorphic_facies|_and_psychomotor_retardation": 1,
    "Osteogenesis_imperfecta_type_9": 27,
    "not_provided|PPIB-related_disorder": 1,
    "Osteogenesis_imperfecta_type_9|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|not_specified|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_9|Osteogenesis_imperfecta|not_provided": 1,
    "PPIB-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Osteogenesis_imperfecta_type_9": 6,
    "PPIB-related_disorder": 4,
    "not_provided|Osteogenesis_imperfecta_type_9|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_9": 1,
    "Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_9": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_9|Inborn_genetic_diseases": 1,
    "not_specified|Osteogenesis_imperfecta_type_9|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_9|not_specified": 1,
    "PPIB-related_disorder|not_provided|Osteogenesis_imperfecta_type_9": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_9": 1,
    "PPIB-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PPIB-related_disorder|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_9|Osteogenesis_imperfecta": 1,
    "not_specified|Osteogenesis_Imperfecta|_Recessive|not_provided": 1,
    "CSNK1G1-related_developmental_disorder_with_autism_spectrum_disorder": 1,
    "TRIP4-related_disorder|not_provided": 5,
    "not_provided|TRIP4-related_disorder": 5,
    "TRIP4-related_disorder": 3,
    "Congenital_muscular_dystrophy-respiratory_failure-skin_abnormalities-joint_hyperlaxity_syndrome|Spinal_muscular_atrophy_with_congenital_bone_fractures_1|not_provided": 1,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_1": 6,
    "not_provided|Spinal_muscular_atrophy_with_congenital_bone_fractures_1": 3,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_1|not_provided": 1,
    "not_specified|Spinal_muscular_atrophy_with_congenital_bone_fractures_1": 1,
    "Congenital_muscular_dystrophy-respiratory_failure-skin_abnormalities-joint_hyperlaxity_syndrome": 3,
    "Spinal_muscular_atrophy_with_congenital_bone_fractures_1|Congenital_muscular_dystrophy-respiratory_failure-skin_abnormalities-joint_hyperlaxity_syndrome|not_provided": 1,
    "not_provided|Congenital_muscular_dystrophy-respiratory_failure-skin_abnormalities-joint_hyperlaxity_syndrome|Spinal_muscular_atrophy_with_congenital_bone_fractures_1": 2,
    "TRIP4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_muscular_dystrophy-respiratory_failure-skin_abnormalities-joint_hyperlaxity_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Recurrent_spontaneous_abortion": 1,
    "Internal_carotid_artery_stenosis": 1,
    "not_provided|Mast_syndrome": 7,
    "Mast_syndrome": 66,
    "SPG21-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Mast_syndrome|not_provided|not_specified": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Mast_syndrome": 1,
    "Hereditary_spastic_paraplegia|not_provided|Mast_syndrome|not_specified": 1,
    "Mast_syndrome|not_specified": 2,
    "SPG21-related_disorder|Hereditary_spastic_paraplegia|Mast_syndrome": 1,
    "Hereditary_spastic_paraplegia|Mast_syndrome": 1,
    "not_provided|Hereditary_spastic_paraplegia|Mast_syndrome|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia|Mast_syndrome|SPG21-related_disorder": 1,
    "not_specified|not_provided|Mast_syndrome": 1,
    "Mast_syndrome|not_provided": 3,
    "Mast_syndrome|Hereditary_spastic_paraplegia": 3,
    "not_provided|not_specified|Mast_syndrome": 1,
    "Hereditary_spastic_paraplegia|Mast_syndrome|not_provided": 1,
    "not_specified|Mast_syndrome": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_15|Mitochondrial_complex_I_deficiency|_nuclear_type_27": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_15|Mitochondrial_complex_I_deficiency|_nuclear_type_27": 1,
    "Combined_oxidative_phosphorylation_defect_type_15": 9,
    "Mitochondrial_oxidative_phosphorylation_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_15|Mitochondrial_complex_I_deficiency|_nuclear_type_27|not_provided": 1,
    "MTFMT-Related_Disorders|Mitochondrial_complex_I_deficiency|_nuclear_type_27|Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_15": 1,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_15": 1,
    "Combined_oxidative_phosphorylation_defect_type_15|not_provided": 4,
    "not_specified|not_provided|MTFMT-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_15|Mitochondrial_complex_I_deficiency|_nuclear_type_27|MTFMT-Related_Disorders|Leigh_syndrome|not_provided|MTFMT-related_disorder|Decreased_activity_of_mitochondrial_complex_I|Inability_to_walk_by_childhood/adolescence|Cytochrome_C_oxidase-negative_muscle_fibers|Abnormal_facial_shape|Short_stature|Poor_speech|See_cases|Inborn_genetic_diseases": 1,
    "MTFMT-related_disorder|not_provided": 3,
    "MTFMT-related_disorder": 3,
    "not_provided|MTFMT-related_disorder": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_27|Combined_oxidative_phosphorylation_defect_type_15|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_15": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_15|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_defect_type_15|Inborn_genetic_diseases": 1,
    "not_specified|MTFMT-related_disorder|not_provided": 1,
    "not_provided|MTFMT-Related_Disorders": 1,
    "not_provided|not_specified|MTFMT-related_disorder": 1,
    "SLC51B-related_disorder": 3,
    "Bile_acid_malabsorption|_primary|_2|Cholestasis|Diarrhea": 1,
    "not_provided|not_specified|SLC51B-related_disorder": 1,
    "not_specified|SLC51B-related_disorder|not_provided": 1,
    "not_provided|SLC51B-related_disorder": 2,
    "SLC51B-related_disorder|not_provided": 1,
    "Nemaline_myopathy_6": 457,
    "not_specified|not_provided|Nemaline_Myopathy|_Dominant": 1,
    "KBTBD13-related_disorder": 3,
    "Nemaline_myopathy_6|not_provided": 22,
    "Nemaline_Myopathy|_Dominant|Nemaline_myopathy_6": 1,
    "not_provided|Nemaline_myopathy_6": 14,
    "not_provided|Nemaline_myopathy_6|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Nemaline_myopathy_6": 31,
    "Nemaline_myopathy_6|Inborn_genetic_diseases": 30,
    "not_specified|not_provided|Nemaline_myopathy_6": 7,
    "KBTBD13-related_disorder|Inborn_genetic_diseases|Nemaline_myopathy_6": 2,
    "not_specified|Nemaline_myopathy_6|not_provided": 4,
    "Nemaline_myopathy_6|KBTBD13-related_disorder": 5,
    "Nemaline_myopathy_6|not_specified": 12,
    "Nemaline_myopathy_6|not_specified|not_provided": 3,
    "not_specified|Nemaline_myopathy_6": 3,
    "Nemaline_myopathy_6|KBTBD13-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Nemaline_myopathy_6": 5,
    "not_provided|Nemaline_myopathy_6|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Nemaline_myopathy_6": 1,
    "not_provided|not_specified|Nemaline_myopathy_6": 1,
    "not_provided|Inborn_genetic_diseases|Nemaline_myopathy_6": 1,
    "not_provided|Nemaline_myopathy_6|KBTBD13-related_disorder": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_6|KBTBD13-related_disorder": 2,
    "KBTBD13-related_disorder|not_provided|Nemaline_myopathy_6": 1,
    "KBTBD13-related_disorder|Nemaline_myopathy_6": 1,
    "Nemaline_myopathy_6|Inborn_genetic_diseases|not_provided": 2,
    "KBTBD13-related_disorder|not_specified|not_provided|Nemaline_myopathy_6": 1,
    "Nemaline_myopathy_6|not_provided|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_12|Nemaline_myopathy_6": 1,
    "not_specified|Nemaline_myopathy_6|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Nemaline_myopathy_6|KBTBD13-related_disorder": 1,
    "Nemaline_Myopathy|_Dominant": 5,
    "not_provided|Nemaline_Myopathy|_Dominant": 1,
    "not_provided|Retinal_dystrophy|Tooth_agenesis|_selective|_7": 1,
    "CLPX-related_disorder": 2,
    "not_provided|CLPX-related_disorder": 1,
    "not_provided|Protoporphyria|_erythropoietic|_2": 1,
    "Protoporphyria|_erythropoietic|_2": 1,
    "CLPX-related_disorder|not_provided": 4,
    "Protoporphyria|_erythropoietic|_2|not_provided": 1,
    "CILP-related_disorder": 9,
    "CILP-related_disorder|Lumbar_disc_disease|_susceptibility_to": 1,
    "RNU5A-1-associated_neurodevelopmental_disorder|not_provided": 2,
    "RNU5B-1-associated_neurodevelopmental_disorder|not_provided": 2,
    "not_provided|RNU5B-1-associated_neurodevelopmental_disorder|RNU5B-1_related_disorder": 1,
    "RNU5B-1_related_disorder": 1,
    "RNU5B-1_related_disorder|RNU5B-1-associated_neurodevelopmental_disorder|Neurodevelopmental_disorder": 1,
    "IGDCC4-related_developmental_disorder": 1,
    "Congenital_stationary_night_blindness_1D": 49,
    "Congenital_stationary_night_blindness_1D|not_provided": 27,
    "not_provided|Congenital_stationary_night_blindness_1D": 12,
    "Inborn_genetic_diseases|Congenital_Stationary_Night_Blindness|_Recessive|not_provided": 1,
    "Retinitis_pigmentosa|Congenital_stationary_night_blindness_1D": 1,
    "not_provided|not_specified|Congenital_stationary_night_blindness_1D": 1,
    "Congenital_stationary_night_blindness_1D|Inborn_genetic_diseases": 2,
    "not_provided|SLC24A1-related_disorder": 3,
    "Congenital_stationary_night_blindness_1D|Inborn_genetic_diseases|not_provided": 4,
    "Congenital_stationary_night_blindness_1D|Retinitis_pigmentosa|not_provided|SLC24A1-related_disorder|Congenital_stationary_night_blindness_autosomal_dominant_2|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_stationary_night_blindness_1D": 5,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1D": 3,
    "not_provided|Congenital_stationary_night_blindness_1D|not_specified": 2,
    "SLC24A1-related_disorder|not_provided": 6,
    "not_provided|SLC24A1-related_disorder|Inborn_genetic_diseases": 1,
    "SLC24A1-related_disorder": 2,
    "Congenital_stationary_night_blindness_1D|not_specified|not_provided": 2,
    "SLC24A1-related_disorder|not_provided|Congenital_stationary_night_blindness_1D": 1,
    "Congenital_stationary_night_blindness_1D|SLC24A1-related_disorder|not_provided": 3,
    "Congenital_stationary_night_blindness_1D|SLC24A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Retinal_dystrophy|Congenital_stationary_night_blindness_1D": 1,
    "RAB11A-associated_neurodevelopmental_condition": 1,
    "not_provided|RAB11A-related_disorder": 2,
    "RAB11A-related_disorder|not_provided": 1,
    "Delayed_speech_and_language_development|Intellectual_disability|_mild|Primary_microcephaly|Precocious_puberty_in_females|Delayed_fine_motor_development|EEG_abnormality|Coarse_facial_features": 1,
    "Noonan_syndrome|not_provided|Cardio-facio-cutaneous_syndrome": 1,
    "Melorheostosis|Cardiofaciocutaneous_syndrome_3": 10,
    "MAP2K1-related_disorder": 2,
    "RASopathy|Cardiofaciocutaneous_syndrome_3": 2,
    "not_specified|RASopathy|Cardiofaciocutaneous_syndrome_3|Melorheostosis": 1,
    "RASopathy|not_specified|MAP2K1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiofaciocutaneous_syndrome_3|Melorheostosis|RASopathy": 1,
    "MAP2K1-related_disorder|RASopathy": 2,
    "Cardio-facio-cutaneous_syndrome|not_specified|RASopathy|Cardiofaciocutaneous_syndrome_3": 1,
    "Cardiofaciocutaneous_syndrome_3": 17,
    "Cardio-facio-cutaneous_syndrome|Cardiofaciocutaneous_syndrome_3|RASopathy|not_provided": 1,
    "not_provided|Melorheostosis|Non-small_cell_lung_carcinoma|Extracranial_arteriovenous_malformation": 1,
    "Melorheostosis": 1,
    "Extracranial_arteriovenous_malformation": 1,
    "Vascular_malformation|Cardio-facio-cutaneous_syndrome|Melorheostosis|not_provided": 1,
    "Parkes_Weber_syndrome|Vascular_malformation": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_3|not_provided": 1,
    "Melorheostosis|Cardiofaciocutaneous_syndrome_3|Cardiovascular_phenotype|MAP2K1-related_RASopathy|Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Autism_spectrum_disorder|Cardiofaciocutaneous_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Cardiofaciocutaneous_syndrome_3|Noonan_syndrome_1|Melorheostosis|RASopathy": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 2,
    "Cardio-facio-cutaneous_syndrome|RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|RASopathy|MAP2K1-related_disorder": 1,
    "Cardiofaciocutaneous_syndrome_3|Melorheostosis|Noonan_syndrome_1|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "not_specified|not_provided|Melorheostosis|Cardiofaciocutaneous_syndrome_3|Noonan_syndrome_1|RASopathy": 1,
    "Squamous_cell_lung_carcinoma|not_provided|not_specified|Cardiofaciocutaneous_syndrome_3": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Obesity": 1,
    "MAP2K1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "Cardiofaciocutaneous_syndrome_3|RASopathy": 2,
    "Cardiovascular_phenotype|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_specified": 1,
    "not_provided|Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_3|RASopathy": 1,
    "MAP2K1-related_rasopathy-like_syndrome|RASopathy|not_provided|MAP2K1-related_disorder": 1,
    "Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_3|RASopathy|Noonan_syndrome": 1,
    "RASopathy|Noonan_syndrome|Cardiofaciocutaneous_syndrome_3|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_3|Cardio-facio-cutaneous_syndrome": 1,
    "Cardiofaciocutaneous_syndrome_3|Cardio-facio-cutaneous_syndrome|RASopathy|not_provided": 1,
    "Cardio-facio-cutaneous_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Cardiovascular_phenotype|MAP2K1-related_disorder|Cardiofaciocutaneous_syndrome_3|Noonan_syndrome_1|Cardio-facio-cutaneous_syndrome|not_provided|RASopathy|Melorheostosis|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiofaciocutaneous_syndrome_3|RASopathy|Melorheostosis": 1,
    "Cardiofaciocutaneous_syndrome_3|not_provided|RASopathy|not_specified": 1,
    "not_provided|not_specified|RASopathy|MAP2K1-related_disorder": 1,
    "RASopathy|Melorheostosis|Cardiofaciocutaneous_syndrome_3": 3,
    "not_provided|Cardiofaciocutaneous_syndrome_3|RASopathy": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_3|Melorheostosis": 3,
    "Inborn_genetic_diseases|Cardiofaciocutaneous_syndrome_3": 1,
    "Noonan_syndrome|RASopathy|not_provided": 2,
    "RASopathy|not_specified|MAP2K1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|MAP2K1-related_disorder": 1,
    "RASopathy|MAP2K1-related_disorder": 1,
    "Noonan_syndrome_1|Cardiofaciocutaneous_syndrome_3|Melorheostosis|RASopathy": 1,
    "Noonan_syndrome|RASopathy|not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|not_provided": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|RASopathy|Cardiovascular_phenotype|MAP2K1-related_disorder": 1,
    "MAP2K1-related_disorder|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "Cardiofaciocutaneous_syndrome_3|Melorheostosis|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|MAP2K1-related_disorder": 1,
    "RASopathy|not_specified|MAP2K1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "RASopathy|not_specified|Melorheostosis|Cardiofaciocutaneous_syndrome_3": 1,
    "RASopathy|not_specified|Cardiofaciocutaneous_syndrome_3|Melorheostosis": 1,
    "Cardiovascular_phenotype|MAP2K1-related_disorder|RASopathy": 1,
    "Cardiofaciocutaneous_syndrome_3|Melorheostosis|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "MAP2K1-related_disorder|Cardiovascular_phenotype|RASopathy|not_provided|not_specified": 1,
    "RASopathy|Cardiovascular_phenotype|not_provided|Cardiofaciocutaneous_syndrome_3|Noonan_syndrome_1": 1,
    "RASopathy|not_provided|not_specified|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Melorheostosis|Cardiofaciocutaneous_syndrome_3|Noonan_syndrome_1|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardio-facio-cutaneous_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome": 1,
    "MAP2K1-related_disorder|not_specified|not_provided|RASopathy": 1,
    "RASopathy|Melorheostosis|Cardiofaciocutaneous_syndrome_3|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|MAP2K1-related_disorder|not_provided|not_specified|RASopathy": 1,
    "Cardiofaciocutaneous_syndrome_3|Melorheostosis|Noonan_syndrome_1|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "Cardiovascular_phenotype|MAP2K1-related_disorder|not_provided|RASopathy": 1,
    "Cardiofaciocutaneous_syndrome_3|Melorheostosis|RASopathy|not_provided": 1,
    "Melorheostosis|Cardiofaciocutaneous_syndrome_3|not_specified": 1,
    "SMAD6-related_disorder": 22,
    "Polydactyly|Radioulnar_synostosis|not_provided|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2|Inborn_genetic_diseases": 103,
    "Inborn_genetic_diseases|Aortic_valve_disease_2": 95,
    "not_provided|Aortic_valve_disease_2|SMAD6-related_disorder": 1,
    "Aortic_valve_disease_2|SMAD6-related_disorder": 2,
    "Aortic_valve_disease_1|not_provided|Radioulnar_synostosis|Aortic_valve_disease_2|Aneurysm-osteoarthritis_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Aortic_valve_disease_2|not_specified": 1,
    "Craniosynostosis_7|Aortic_valve_disease_2|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to": 1,
    "not_specified|Aortic_valve_disease_2|not_provided|Craniosynostosis_7": 1,
    "SMAD6-related_disorder|Aortic_valve_disease_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Aortic_valve_disease_2|Inborn_genetic_diseases": 5,
    "Radioulnar_synostosis|Heart|_malformation_of|Bicuspid_aortic_valve": 1,
    "Aortic_valve_disease_2|Inborn_genetic_diseases|not_specified": 5,
    "SMAD6-related_disorder|Inborn_genetic_diseases|not_specified|Aortic_valve_disease_2": 1,
    "not_provided|Radioulnar_synostosis": 3,
    "not_specified|Aortic_valve_disease_2": 7,
    "not_specified|Aortic_valve_disease_2|Inborn_genetic_diseases": 4,
    "Abnormal_axial_skeleton_morphology|Radioulnar_synostosis": 1,
    "Aortic_valve_disease_2|Inborn_genetic_diseases|SMAD6-related_disorder": 2,
    "Inborn_genetic_diseases|Aortic_valve_disease_2|not_provided": 2,
    "Aortic_valve_disease_2|not_provided|Radioulnar_synostosis": 2,
    "Radioulnar_synostosis|not_provided|Aortic_valve_disease_2": 2,
    "not_specified|Aortic_valve_disease_2|Inborn_genetic_diseases|SMAD6-related_disorder": 1,
    "Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Craniosynostosis_7|Aortic_valve_disease_2|Abnormal_axial_skeleton_morphology|Radioulnar_synostosis": 1,
    "not_specified|Inborn_genetic_diseases|Aortic_valve_disease_2|not_provided": 1,
    "Craniosynostosis_7|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2|Radioulnar_synostosis|Craniosynostosis_7": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Aortic_valve_disease_2": 1,
    "Inborn_genetic_diseases|not_provided|Aortic_valve_disease_2": 2,
    "Aortic_valve_disease_2|not_specified|Inborn_genetic_diseases": 6,
    "not_specified|Inborn_genetic_diseases|not_provided|Aortic_valve_disease_2": 1,
    "Plagiocephaly|Radioulnar_synostosis": 1,
    "Aortic_valve_disease_2|Inborn_genetic_diseases|SMAD6-related_disorder|Craniosynostosis_7": 1,
    "not_specified|Radioulnar_synostosis": 1,
    "Aortic_valve_disease_2|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Aortic_valve_disease_2|not_provided": 1,
    "not_provided|Aortic_valve_disease_2|Radioulnar_synostosis": 2,
    "Radioulnar_synostosis|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Craniosynostosis_7|Craniosynostosis_syndrome|Aortic_valve_disease_2|not_provided": 1,
    "Aortic_valve_disease_2|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Craniosynostosis_7": 2,
    "Aortic_valve_disease_2|not_specified|not_provided": 3,
    "SMAD6-related_disorder|not_provided|Radioulnar_synostosis|Aortic_valve_disease_2": 1,
    "Radioulnar_synostosis|_nonsyndromic|_susceptibility_to": 2,
    "Inborn_genetic_diseases|SMAD6-related_disorder|Aortic_valve_disease_2": 2,
    "Aortic_valve_disease_2|not_provided|Inborn_genetic_diseases": 2,
    "SMAD6-related_disorder|Inborn_genetic_diseases|Aortic_valve_disease_2": 5,
    "Radioulnar_synostosis|Frontal_bossing|Premature_closure_of_fontanelles|Plagiocephaly|Thoracic_aortic_aneurysm": 1,
    "Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Radioulnar_synostosis": 2,
    "not_provided|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Radioulnar_synostosis|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2|not_provided|CRANIOSYNOSTOSIS_7|_SUSCEPTIBILITY_TO": 2,
    "Aortic_valve_disease_2|Aortic_valve_disease_1": 1,
    "Inborn_genetic_diseases|Aortic_valve_disease_2|Radioulnar_synostosis": 1,
    "Aortic_valve_disease_1|Aortic_valve_disease_2|not_provided": 1,
    "Aortic_valve_disease_2|Radioulnar_synostosis": 1,
    "SMAD6-related_disorder|Aortic_valve_disease_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Aortic_valve_disease_2|not_provided|not_specified": 1,
    "Craniosynostosis_7|Aortic_valve_disease_2|not_specified|Inborn_genetic_diseases": 1,
    "Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Craniosynostosis_7": 1,
    "Aortic_valve_disease_1|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2|Craniosynostosis_7|SMAD6-related_disorder": 1,
    "not_specified|Aortic_valve_disease_2|SMAD6-related_disorder": 1,
    "SMAD6-related_disorder|Aortic_valve_disease_2": 2,
    "not_provided|Inborn_genetic_diseases|Aortic_valve_disease_2": 1,
    "Inborn_genetic_diseases|Aortic_valve_disease_2|Craniosynostosis_7": 1,
    "Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2|Craniosynostosis_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Aortic_valve_disease_2|not_specified": 1,
    "not_specified|Aortic_valve_disease_2|Craniosynostosis_7": 1,
    "SMAD6-related_disorder|not_provided|Aortic_valve_disease_2|Inborn_genetic_diseases": 1,
    "not_provided|SMAD6-related_disorder|Aortic_valve_disease_2|Craniosynostosis_7": 1,
    "Radioulnar_synostosis|Aortic_valve_disease_2": 1,
    "Radioulnar_synostosis|Heart|_malformation_of": 1,
    "CRANIOSYNOSTOSIS_7|_SUSCEPTIBILITY_TO": 1,
    "Aortic_valve_disease_2|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Radioulnar_synostosis": 1,
    "Aortic_valve_disease_2|Craniosynostosis_7|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|not_provided": 1,
    "Aortic_valve_disease_2|Esophageal_atresia/tracheoesophageal_fistula": 1,
    "not_provided|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to": 1,
    "SMAD6-related_disorder|Inborn_genetic_diseases": 1,
    "Aortic_valve_disease_2|Inborn_genetic_diseases|SMAD6-related_disorder|not_specified": 1,
    "Polydactyly|Radioulnar_synostosis": 1,
    "Inborn_genetic_diseases|not_specified|Aortic_valve_disease_2": 1,
    "Aortic_valve_disease_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Radioulnar_synostosis|Heart|_malformation_of|Premature_closure_of_fontanelles|Frontal_bossing": 1,
    "Aortic_valve_disease_2|Craniosynostosis_7|not_provided": 1,
    "Inborn_genetic_diseases|Aortic_valve_disease_2|SMAD6-related_disorder|not_provided|not_specified": 1,
    "Aortic_valve_disease_2|SMAD6-related_disorder|Inborn_genetic_diseases": 1,
    "Craniosynostosis_7|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Aortic_valve_disease_2": 1,
    "not_provided|Radioulnar_synostosis|_nonsyndromic|_susceptibility_to|Radioulnar_synostosis": 1,
    "Craniosynostosis_7|Aortic_valve_disease_2|not_provided": 1,
    "Craniosynostosis_7|not_specified": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 59,
    "Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome": 10,
    "Aneurysm-osteoarthritis_syndrome": 111,
    "not_specified|Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome": 1,
    "not_specified|not_provided|Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Aneurysm-osteoarthritis_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 51,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|SMAD3-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD3-related_disorder": 1,
    "not_specified|Aneurysm-osteoarthritis_syndrome|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "Aneurysm-osteoarthritis_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "not_provided|Aneurysm-osteoarthritis_syndrome": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_specified": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 10,
    "not_specified|SMAD3-related_disorder": 1,
    "SMAD3-related_disorder": 5,
    "Aneurysm-osteoarthritis_syndrome|not_provided": 4,
    "Aneurysm-osteoarthritis_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aneurysm-osteoarthritis_syndrome": 2,
    "not_provided|Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Aneurysm-osteoarthritis_syndrome|not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|SMAD3-related_disorder|not_provided|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aneurysm-osteoarthritis_syndrome": 7,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|SMAD3-related_disorder|Cardiovascular_phenotype": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_provided": 11,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta": 1,
    "Aneurysm-osteoarthritis_syndrome|Vascular_dilatation": 1,
    "Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thoracic_aortic_aneurysm|not_specified|not_provided|Aneurysm-osteoarthritis_syndrome": 1,
    "Aneurysm-osteoarthritis_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_specified|not_provided|SMAD3-related_disorder": 1,
    "Loeys-Dietz_syndrome|Aneurysm-osteoarthritis_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "SMAD3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 2,
    "Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thoracic_aortic_aneurysm|not_specified|not_provided|Ehlers-Danlos_syndrome|Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome": 1,
    "not_specified|SMAD3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Coronary_artery_disorder|not_provided": 1,
    "not_specified|Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 3,
    "SMAD3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Aneurysm-osteoarthritis_syndrome|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aneurysm-osteoarthritis_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome|not_provided|SMAD3-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Aneurysm-osteoarthritis_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD3-related_disorder": 1,
    "Ehlers-Danlos_syndrome|not_provided|Aneurysm-osteoarthritis_syndrome": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD3-related_disorder|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_aortopathy": 1,
    "SMAD3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_provided": 1,
    "Familial_aortopathy|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome": 1,
    "See_cases|SMAD3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|SMAD3-related_disorder|not_provided": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "not_provided|SMAD3-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome|not_provided|Ehlers-Danlos_syndrome": 1,
    "Connective_tissue_disorder|not_provided|Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aneurysm-osteoarthritis_syndrome|not_provided|Ehlers-Danlos_syndrome|Loeys-Dietz_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ascending_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Aneurysm-osteoarthritis_syndrome|SMAD3-related_disorder|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 2,
    "Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|SMAD3-related_disorder|not_specified|Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aneurysm-osteoarthritis_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD3-related_disorder": 1,
    "Aneurysm-osteoarthritis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD3-related_disorder": 1,
    "Ehlers-Danlos_syndrome|Aneurysm-osteoarthritis_syndrome": 1,
    "SMAD3-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 2,
    "Aneurysm-osteoarthritis_syndrome|Loeys-Dietz_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|not_specified": 1,
    "not_specified|Isolated_thoracic_aortic_aneurysm|Cardiovascular_phenotype|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "not_specified|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD3-related_disorder|not_provided": 1,
    "Arterial_dissection|Cutaneous_polyarteritis_nodosa|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aneurysm-osteoarthritis_syndrome": 1,
    "Aneurysm-osteoarthritis_syndrome|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|See_cases": 1,
    "Ehlers-Danlos_syndrome|Aneurysm-osteoarthritis_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aneurysm-osteoarthritis_syndrome|Cardiovascular_phenotype": 1,
    "Aneurysm-osteoarthritis_syndrome|Ehlers-Danlos_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aneurysm-osteoarthritis_syndrome|not_provided|Loeys-Dietz_syndrome": 5,
    "Aneurysm-osteoarthritis_syndrome|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Palmoplantar_keratoderma|_punctate_type_1A": 6,
    "Palmoplantar_keratoderma|_punctate_type_1A|not_provided": 6,
    "not_provided|Palmoplantar_keratoderma|_punctate_type_1A|not_specified": 1,
    "not_provided|Palmoplantar_keratoderma|_punctate_type_1A": 6,
    "Neoplasm_of_the_endocrine_system": 1,
    "Palmoplantar_keratoderma": 1,
    "AAGAB-related_disorder": 4,
    "CLN6-related_disorder": 2,
    "Ceroid_lipofuscinosis|_neuronal|_6A": 29,
    "CLN6-related_disorder|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Inborn_genetic_diseases|not_specified|Adult_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|not_provided|Neuronal_ceroid_lipofuscinosis|not_specified|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis|Cystic_fibrosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "CLN6-related_disorder|Neuronal_ceroid_lipofuscinosis|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis": 4,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis": 3,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis": 3,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis": 4,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "not_specified|CLN6-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A|not_provided|Neuronal_ceroid_lipofuscinosis": 3,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 3,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Neuronal_ceroid_lipofuscinosis": 3,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Spastic_ataxia": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A": 4,
    "not_specified|Neuronal_ceroid_lipofuscinosis|not_provided|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Inborn_genetic_diseases|CLN6-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|CLN6-related_disorder": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 9,
    "Ceroid_lipofuscinosis|_neuronal|_6A|not_provided": 2,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "Adult_neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Agenesis_of_the_corpus_callosum_with_peripheral_neuropathy|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Inborn_genetic_diseases|CLN6-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "Adult_neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|not_provided|Neuronal_ceroid_lipofuscinosis|See_cases": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|not_provided|Neuronal_ceroid_lipofuscinosis": 3,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Inborn_genetic_diseases": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Abnormal_brain_morphology|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Abnormality_of_the_nervous_system": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|See_cases|not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A|not_specified": 1,
    "not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A": 3,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Neuronal_ceroid_lipofuscinosis": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|not_specified|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A|not_provided|not_specified": 1,
    "not_provided|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|not_provided|Inborn_genetic_diseases": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 2,
    "not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|not_specified": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|CLN6-related_disorder|Adult_neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_6A": 1,
    "not_specified|not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Ceroid_lipofuscinosis|_neuronal|_6A|Adult_neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Ceroid_lipofuscinosis|_neuronal|_6A|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Ceroid_lipofuscinosis|_neuronal|_6A|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Ceroid_lipofuscinosis|_neuronal|_6A|Ceroid_lipofuscinosis|_neuronal|_6B_(Kufs_type)|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_BEHAVIORAL|_EAR|_AND_SKELETAL_ABNORMALITIES": 1,
    "not_provided|KIF23-related_disorder": 10,
    "KIF23-related_disorder|not_provided": 6,
    "KIF23-related_disorder": 4,
    "not_provided|KIF23-related_disorder|not_specified": 1,
    "not_provided|not_specified|KIF23-related_disorder": 1,
    "Congenital_dyserythropoietic_anemia|_type_III": 6,
    "Congenital_dyserythropoietic_anemia|_type_III|not_provided|not_specified": 1,
    "TLE3-related_condition": 1,
    "not_specified|TLE3-related_condition": 1,
    "UACA-related_disorder": 31,
    "not_provided|UACA-related_disorder": 2,
    "not_provided|not_specified|UACA-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_12": 18,
    "Aortic_aneurysm|_familial_thoracic_12|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|THSD4-related_disorder": 1,
    "not_provided|THSD4-related_disorder|not_specified": 1,
    "THSD4-related_disorder": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_12": 1,
    "not_provided|THSD4-related_disorder": 1,
    "Retinitis_pigmentosa|not_provided|Enhanced_S-cone_syndrome": 1,
    "Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive": 4,
    "Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive": 2,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37": 9,
    "Enhanced_S-cone_syndrome|not_provided": 40,
    "Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome": 5,
    "not_provided|Retinitis_pigmentosa|Enhanced_S-cone_syndrome": 2,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided": 9,
    "Goldmann-Favre_syndrome": 5,
    "Enhanced_S-cone_syndrome": 47,
    "Inborn_genetic_diseases|Goldmann-Favre_syndrome|not_provided": 2,
    "not_provided|Enhanced_S-cone_syndrome|NR2E3-related_disorder": 1,
    "Goldmann-Favre_syndrome|not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37": 1,
    "Enhanced_S-cone_syndrome|not_provided|NR2E3-related_disorder": 2,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided": 5,
    "NR2E3-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Horizontal_nystagmus|Color_vision_defect|Visual_impairment|not_specified|Ocular_albinism|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Goldmann-Favre_syndrome|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy": 1,
    "not_provided|Enhanced_S-cone_syndrome": 15,
    "not_provided|Goldmann-Favre_syndrome": 10,
    "Goldmann-Favre_syndrome|not_provided|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|Goldmann-Favre_syndrome|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided": 6,
    "not_provided|Enhanced_S-cone_syndrome|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Goldmann-Favre_syndrome": 1,
    "Retinal_dystrophy|not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37": 2,
    "NR2E3-related_disorder|not_provided": 5,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_37": 1,
    "not_provided|Inborn_genetic_diseases|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Retinal_dystrophy|Goldmann-Favre_syndrome": 1,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|NR2E3-related_disorder|not_provided": 1,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "NR2E3-related_disorder": 3,
    "Goldmann-Favre_syndrome|not_provided": 6,
    "not_provided|Atypical_retinitis_pigmentosa": 1,
    "not_provided|NR2E3-related_disorder": 2,
    "NR2E3-related_disorder|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided": 3,
    "NR2E3-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Enhanced_S-cone_syndrome": 1,
    "NR2E3-related_disorder|Retinal_dystrophy|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided|Goldmann-Favre_syndrome": 1,
    "Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided": 1,
    "not_provided|Optic_atrophy|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37": 1,
    "Retinal_dystrophy|Enhanced_S-cone_syndrome|not_provided": 4,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Enhanced_S-cone_syndrome": 3,
    "not_provided|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa_37": 1,
    "Enhanced_S-cone_syndrome|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|Abnormality_of_the_eye|not_provided": 1,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|Retinal_dystrophy": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided|NR2E3-related_disorder|Retinitis_pigmentosa": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|NR2E3-related_disorder": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_37": 2,
    "NR2E3-related_disorder|Retinal_dystrophy|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|Retinitis_pigmentosa": 1,
    "Enhanced_S-cone_syndrome|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|Retinal_dystrophy|not_provided|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome": 1,
    "Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|not_provided": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|NR2E3-related_disorder": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_provided|Goldmann-Favre_syndrome": 1,
    "Enhanced_S-cone_syndrome|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|NR2E3-related_disorder|not_provided|Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Goldmann-Favre_syndrome": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Enhanced_S-cone_syndrome|Goldmann-Favre_syndrome": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Goldmann-Favre_syndrome|not_provided": 1,
    "Retinitis_pigmentosa|not_specified|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Inborn_genetic_diseases|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|not_provided|Retinitis_pigmentosa_37": 1,
    "Enhanced_S-cone_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Goldmann-Favre_syndrome": 1,
    "Enhanced_S-cone_syndrome|Optic_atrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Goldmann-Favre_syndrome|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided": 1,
    "Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_37": 1,
    "not_specified|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|Goldmann-Favre_syndrome": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Retinal_dystrophy|Cone-rod_dystrophy": 1,
    "Enhanced_S-cone_syndrome|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Goldmann-Favre_syndrome|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided": 1,
    "Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided|Retinal_dystrophy": 1,
    "not_specified|not_provided|Goldmann-Favre_syndrome": 1,
    "not_specified|Enhanced_S-cone_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37": 1,
    "Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa": 4,
    "Retinal_dystrophy|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Goldmann-Favre_syndrome|not_provided": 1,
    "not_provided|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_pigmentosa": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37": 3,
    "Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|NR2E3-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Enhanced_S-cone_syndrome|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|not_provided|not_specified": 1,
    "not_specified|not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Enhanced_S-cone_syndrome|Retinal_dystrophy|not_provided": 1,
    "Enhanced_S-cone_syndrome|not_provided|NR2E3-related_disorder|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Enhanced_S-cone_syndrome": 2,
    "NR2E3-related_disorder|Enhanced_S-cone_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_37|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Goldmann-Favre_syndrome": 1,
    "Autosomal_recessive_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome": 1,
    "Enhanced_S-cone_syndrome|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_37": 1,
    "not_provided|Retinal_dystrophy|Goldmann-Favre_syndrome": 1,
    "not_provided|not_specified|Enhanced_S-cone_syndrome": 1,
    "not_specified|Retinitis_pigmentosa_37|Enhanced_S-cone_syndrome|not_provided|Retinal_dystrophy": 1,
    "NR2E3-related_disorder|not_provided|Enhanced_S-cone_syndrome|Retinal_dystrophy": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_specified|Goldmann-Favre_syndrome": 1,
    "Retinitis_pigmentosa_37|not_provided|Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome": 1,
    "Goldmann-Favre_syndrome|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|not_provided|Retinal_dystrophy": 1,
    "not_provided|Enhanced_S-cone_syndrome|Retinitis_pigmentosa_37|Retinal_dystrophy": 1,
    "Enhanced_S-cone_syndrome|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa|Enhanced_S-cone_syndrome": 3,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Enhanced_S-cone_syndrome": 4,
    "Enhanced_S-cone_syndrome|Retinitis_pigmentosa": 3,
    "Retinitis_Pigmentosa|_Recessive|Enhanced_S-cone_syndrome": 1,
    "Retinitis_Pigmentosa|_Recessive|not_provided|Enhanced_S-cone_syndrome": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_37|not_provided": 1,
    "MYO9A-related_disorder": 13,
    "Myasthenic_syndrome|_congenital|_24|_presynaptic": 16,
    "not_provided|MYO9A-related_disorder": 9,
    "Myasthenic_syndrome|_congenital|_24|_presynaptic|not_provided": 2,
    "Myasthenic_syndrome|_congenital|_24|_presynaptic|Flexion_contracture": 1,
    "Bronchiectasis": 2,
    "not_provided|Myasthenic_syndrome|_congenital|_24|_presynaptic": 3,
    "Inborn_genetic_diseases|Myasthenic_syndrome|_congenital|_24|_presynaptic": 2,
    "MYO9A-related_disorder|not_provided": 2,
    "Myasthenic_syndrome|_congenital|_24|_presynaptic|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis|Myasthenic_syndrome|_congenital|_24|_presynaptic": 1,
    "MYO9A-related_disorder|Myasthenic_syndrome|_congenital|_24|_presynaptic|not_provided": 1,
    "Myasthenic_syndrome|_congenital|_24|_presynaptic|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|MYO9A-related_disorder": 1,
    "not_provided|MYO9A-related_disorder|Myasthenic_syndrome|_congenital|_24|_presynaptic": 1,
    "Inborn_genetic_diseases|MYO9A-related_disorder": 2,
    "Inborn_genetic_diseases|MYO9A-related_disorder|not_provided": 1,
    "MYO9A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|MYO9A-related_disorder": 1,
    "Presynaptic_congenital_myasthenic_syndrome": 4,
    "Myasthenic_syndrome|_congenital|_24|_presynaptic|not_provided|Flexion_contracture": 1,
    "CELF6-related_disorder|not_provided": 1,
    "CELF6-related_disorder": 1,
    "not_provided|Tay-Sachs_disease": 45,
    "Tay-Sachs_disease": 995,
    "Tay-Sachs_disease|HEXA-related_disorder": 2,
    "not_specified|Tay-Sachs_disease": 7,
    "Tay-Sachs_disease|not_specified|not_provided": 4,
    "not_specified|not_provided|Tay-Sachs_disease": 6,
    "not_provided|GM2-GANGLIOSIDOSIS|_JUVENILE|Tay-Sachs_disease": 1,
    "not_specified|not_provided|GM2-GANGLIOSIDOSIS|_CHRONIC|Tay-Sachs_disease": 1,
    "Tay-Sachs_disease|Inborn_genetic_diseases": 19,
    "HEXA-related_disorder|Tay-Sachs_disease": 3,
    "Inborn_genetic_diseases|not_provided|GM2-GANGLIOSIDOSIS|_JUVENILE|Tay-Sachs_disease": 1,
    "Inborn_genetic_diseases|Tay-Sachs_disease|GM2-gangliosidosis|_adult-onset": 1,
    "not_specified|Tay-Sachs_disease|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Tay-Sachs_disease": 4,
    "Inborn_genetic_diseases|Tay-Sachs_disease": 22,
    ".|Tay-Sachs_disease": 2,
    "Inborn_genetic_diseases|Tay-Sachs_disease|not_specified": 1,
    "Inborn_genetic_diseases|HEXA-related_disorder|Tay-Sachs_disease|not_provided": 1,
    "Tay-Sachs_disease|not_specified": 13,
    "GM2-ganglioside_accumulation": 1,
    "Tay-Sachs_disease|not_provided": 22,
    "not_provided|Inborn_genetic_diseases|HEXA-related_disorder|Tay-Sachs_disease": 1,
    "Inborn_genetic_diseases|Tay-Sachs_disease|not_provided": 3,
    "not_provided|Tay-Sachs_disease|HEXA-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Leukodystrophy|Seizure|Hearing_impairment|not_provided|Tay-Sachs_disease|Inborn_genetic_diseases": 1,
    "HEXA-related_disorder|Inborn_genetic_diseases|Tay-Sachs_disease|Tay-Sachs_disease|_variant_AB|not_provided|Intellectual_disability": 1,
    "not_provided|not_specified|Tay-Sachs_disease": 3,
    "not_specified|Tay-Sachs_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Tay-Sachs_disease": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Tay-Sachs_disease": 1,
    "not_provided|Tay-Sachs_disease|not_specified": 4,
    "HEXA-related_disorder|Inborn_genetic_diseases|not_provided|Tay-Sachs_disease": 1,
    "GM2-GANGLIOSIDOSIS|_B1_VARIANT|Tay-Sachs_disease": 1,
    "HEXA-related_disorder|Tay-Sachs_disease|not_provided": 1,
    "not_provided|.|Tay-Sachs_disease": 2,
    "Tay-Sachs_disease|_B1_variant": 1,
    "Neurodevelopmental_abnormality|Tay-Sachs_disease": 1,
    "Tay-Sachs_disease|Inborn_genetic_diseases|not_provided": 1,
    "Tay-Sachs_disease|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Tay-Sachs_disease|GM2-GANGLIOSIDOSIS|_CHRONIC": 1,
    "HEXA-related_disorder|Inborn_genetic_diseases|not_provided|Tay-Sachs_disease|Gm2-gangliosidosis|_adult": 1,
    "not_provided|Tay-Sachs_disease|_B1_variant|Tay-Sachs_disease": 1,
    "TAY-SACHS_DISEASE|_JUVENILE|Tay-Sachs_disease": 1,
    "Hereditary_ataxia|not_specified|not_provided|BETA-HEXOSAMINIDASE_A|_PSEUDODEFICIENCY_OF|Tay-Sachs_disease": 1,
    "not_specified|not_provided|.|Tay-Sachs_disease": 1,
    "Tay-Sachs_disease|HEXA-related_disorder|not_provided": 2,
    "HEXA-related_disorder|Inborn_genetic_diseases|.|Tay-Sachs_disease|_B1_variant|Tay-Sachs_disease|not_provided|Global_developmental_delay": 1,
    "Tay-Sachs_disease|Tay-Sachs_disease|_B1_variant": 1,
    "not_specified|Tay-Sachs_disease|HEXA-related_disorder": 1,
    "Tay-Sachs_disease|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|not_specified|not_provided|HEXA-related_disorder|Tay-Sachs_disease": 1,
    "not_provided|Tay-Sachs_disease|HEXA-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|ARIH1-related_disorder|not_provided": 1,
    "Aortic_aneurysm|not_provided": 1,
    "ARIH1-related_disorder|not_specified|not_provided": 1,
    "not_provided|ARIH1-related_disorder": 1,
    "ARIH1-related_disorder|not_provided": 6,
    "not_provided|ARIH1-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Bardet-Biedl_syndrome_4": 101,
    "not_specified|not_provided|Bardet-Biedl_syndrome_4": 1,
    "Bardet-Biedl_syndrome_4|not_provided|not_specified": 1,
    "BBS4-related_disorder": 49,
    "Bardet-Biedl_syndrome_4|not_provided": 4,
    "Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome|BBS4-related_disorder": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_4": 1,
    "BBS4-related_disorder|Bardet-Biedl_syndrome": 24,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 32,
    "Bardet-Biedl_syndrome|BBS4-related_disorder": 21,
    "Bardet-Biedl_syndrome_4|not_specified|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 34,
    "BBS4-related_disorder|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 3,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|BBS4-related_disorder": 7,
    "Bardet-Biedl_syndrome_1|not_specified|Bardet-Biedl_syndrome_4|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_specified|not_provided|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome_1": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|BBS4-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_4": 2,
    "BBS4-related_disorder|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 8,
    "not_provided|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome|not_provided|not_specified": 1,
    "BBS4-related_disorder|Bardet-Biedl_syndrome_4": 4,
    "BBS4-related_disorder|Inborn_genetic_diseases|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 1,
    "Bardet-Biedl_syndrome|BBS4-related_disorder|Bardet-Biedl_syndrome_4": 7,
    "not_provided|BBS4-related_disorder|Bardet-Biedl_syndrome": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS4-related_disorder|Bardet-Biedl_syndrome_4": 1,
    "not_provided|Bardet-Biedl_syndrome_4": 5,
    "Bardet-Biedl_syndrome|BBS4-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|BBS4-related_disorder": 1,
    "Bardet-Biedl_syndrome|not_provided|not_specified|BBS4-related_disorder": 1,
    "BBS4-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 4,
    "Bardet-Biedl_syndrome_4|BBS4-related_disorder": 3,
    "Bardet-Biedl_syndrome_4|Inborn_genetic_diseases": 2,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|BBS4-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_4": 2,
    "BBS4-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "BBS4-related_disorder|Retinal_dystrophy": 1,
    "not_provided|Bardet-Biedl_syndrome_4|BBS4-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_4|BBS4-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "BBS4-related_disorder|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome_4|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|not_provided|not_specified": 1,
    "Bardet-Biedl_syndrome|Retinal_dystrophy|BBS4-related_disorder|Bardet-Biedl_syndrome_4": 1,
    "BBS4-related_disorder|not_provided|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 2,
    "not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa|Bardet-Biedl_syndrome_4": 1,
    "Inborn_genetic_diseases|BBS4-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|not_provided": 1,
    "Bardet-Biedl_syndrome_4|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4|BBS4-related_disorder": 2,
    "not_provided|BBS4-related_disorder|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 1,
    "BBS4-related_disorder|not_provided": 1,
    "not_specified|BBS4-related_disorder|Bardet-Biedl_syndrome": 1,
    "BBS4-related_disorder|not_provided|Bardet-Biedl_syndrome": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|not_specified": 1,
    "Bardet-Biedl_syndrome_4|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_4|BBS4-related_disorder|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome_4|not_provided|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_4": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 2,
    "not_specified|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_4": 2,
    "BBS4-related_disorder|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_4|not_provided|BBS4-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS4-related_disorder|Bardet-Biedl_syndrome_4": 1,
    "Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome|not_provided": 1,
    "BBS4-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|BBS4-related_disorder|Bardet-Biedl_syndrome_4|not_specified": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_4|BBS4-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome|BBS4-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_4": 1,
    "Inborn_genetic_diseases|BBS4-related_disorder|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome|BBS4-related_disorder|Retinitis_pigmentosa": 1,
    "BBS4-related_disorder|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_4|not_provided|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_4|Bardet-Biedl_syndrome|BBS4-related_disorder": 1,
    "not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_4": 1,
    "NEO1-related_disorder": 29,
    "NEO1-related_disorder|not_provided": 1,
    "not_provided|NEO1-related_disorder": 2,
    "Sick_sinus_syndrome_2|_autosomal_dominant": 36,
    "Sick_sinus_syndrome_2|_autosomal_dominant|not_provided": 3,
    "not_provided|Sick_sinus_syndrome_2|_autosomal_dominant": 11,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 3,
    "Brugada_syndrome_8|Cardiovascular_phenotype": 198,
    "Cardiovascular_phenotype|Brugada_syndrome_8": 186,
    "Brugada_syndrome_8|not_specified|Cardiovascular_phenotype": 7,
    "Brugada_syndrome_8|not_specified|not_provided|Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Brugada_syndrome_8": 865,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_provided": 17,
    "not_specified|Cardiovascular_phenotype|not_provided|Brugada_syndrome_8": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|not_provided": 15,
    "Brugada_syndrome_8|not_specified|not_provided|Cardiovascular_phenotype": 6,
    "not_provided|Brugada_syndrome_8|Cardiovascular_phenotype": 12,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_8|HCN4-related_disorder|not_specified": 1,
    "not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Brugada_syndrome_8|HCN4-related_disorder": 2,
    "not_provided|Brugada_syndrome_8|Cardiovascular_phenotype|not_specified": 2,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Cardiovascular_phenotype|not_provided|Sinoatrial_node_disorder": 1,
    "not_specified|not_provided|Brugada_syndrome_8|Cardiovascular_phenotype|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Cardiovascular_phenotype": 4,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_8": 15,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 3,
    "not_provided|Cardiovascular_phenotype|not_specified|Brugada_syndrome_8": 2,
    "not_specified|Brugada_syndrome_8": 8,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_8": 23,
    "Brugada_syndrome_8|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|not_provided": 19,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_8": 6,
    "not_provided|Brugada_syndrome_8": 19,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 3,
    "not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|not_provided|Cardiovascular_phenotype": 12,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 6,
    "Brugada_syndrome_8|not_specified": 9,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_8": 2,
    "Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_specified": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_provided|Cardiovascular_phenotype": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_specified|not_provided|Cardiomyopathy": 1,
    "HCN4-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_8": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Cardiovascular_phenotype|not_provided": 3,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|not_specified": 1,
    "not_provided|not_specified|Brugada_syndrome_8|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Cardiomyopathy": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype|not_provided": 2,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 4,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_provided": 1,
    "Cardiovascular_phenotype|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|not_provided": 1,
    "Brugada_syndrome_8|not_specified|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Cardiovascular_phenotype": 1,
    "HCN4-related_disorder|Cardiovascular_phenotype|not_provided|Brugada_syndrome_8": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_provided|HCN4-related_disorder": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|Left_ventricular_noncompaction|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Brugada_syndrome_8|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant": 3,
    "HCN4-related_disorder|Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype|Brugada_syndrome_8": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Brugada_syndrome_8": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_specified": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome_8|not_provided": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|HCN4-related_disorder|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|not_provided|Cardiovascular_phenotype": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|HCN4-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|not_provided": 2,
    "not_provided|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 6,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|not_specified|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|Brugada_syndrome_8|HCN4-related_disorder|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Cardiovascular_phenotype|not_specified": 1,
    "Brugada_syndrome_8|not_provided|HCN4-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Atrial_fibrillation|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_8|not_specified": 4,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|not_provided": 2,
    "not_specified|Brugada_syndrome_8|HCN4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|HCN4-related_disorder|Brugada_syndrome_8|not_provided": 1,
    "Brugada_syndrome_8|HCN4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Brugada_syndrome_8|not_provided|not_specified|HCN4-related_disorder": 1,
    "Brugada_syndrome_8|HCN4-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Atrial_fibrillation|Hypertrophic_cardiomyopathy|Ventricular_tachycardia|not_specified|not_provided|Left_ventricular_noncompaction|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Brugada_syndrome_8": 1,
    "HCN4-related_disorder|not_specified|Brugada_syndrome_8|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|not_specified|Brugada_syndrome_8": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_provided": 1,
    "Cardiovascular_phenotype|HCN4-related_disorder|not_provided|Brugada_syndrome_8": 2,
    "not_specified|Cardiovascular_phenotype|Brugada_syndrome_8": 3,
    "not_specified|Brugada_syndrome_8|Cardiovascular_phenotype": 2,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_provided|Cardiomyopathy": 1,
    "Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Cardiovascular_phenotype|not_provided": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 1,
    "Cardiovascular_phenotype|Sudden_cardiac_death|not_specified|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_8|Cardiac_arrhythmia": 1,
    "Brugada_syndrome_8|not_specified|Cardiovascular_phenotype|Cardiac_arrest|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Brugada_syndrome_8|not_specified|HCN4-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "HCN4-related_disorder": 2,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_specified|HCN4-related_disorder": 1,
    "HCN4-related_disorder|not_provided|Brugada_syndrome_8|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Brugada_syndrome_8|not_specified|Cardiovascular_phenotype": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|not_provided": 1,
    "not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Sudden_cardiac_death|Sinus_bradycardia": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|not_provided|HCN4-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_provided|Ventricular_tachycardia": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Brugada_syndrome_8|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_specified|not_provided": 1,
    "Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Brugada_syndrome_8": 3,
    "Ventricular_tachycardia|Brugada_syndrome_8|not_provided": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|not_specified": 2,
    "not_provided|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Brugada_syndrome_8": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|not_specified|not_provided|Brugada_syndrome_8": 1,
    "not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 3,
    "Brugada_syndrome_8|not_specified|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype|not_provided": 1,
    "HCN4-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "HCN4-related_disorder|Brugada_syndrome_8": 4,
    "HCN4-related_disorder|not_provided|Brugada_syndrome_8": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|not_specified": 1,
    "HCN4-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_8": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_provided|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|HCN4-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "Brugada_syndrome_8|not_specified|not_provided": 1,
    "not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|not_provided": 1,
    "HCN4-related_disorder|Brugada_syndrome_8|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "not_provided|not_specified|HCN4-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_8": 1,
    "not_specified|Brugada_syndrome_8|HCN4-related_disorder|Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Congestive_heart_failure": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|Ventricular_tachycardia": 1,
    "Brugada_syndrome_8|not_provided|not_specified": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "not_provided|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype|Brugada_syndrome_8": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_8|not_specified": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Brugada_syndrome_8|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "not_provided|Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Primary_dilated_cardiomyopathy|Brugada_syndrome_8|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|HCN4-related_disorder": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|HCN4-related_disorder|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|Cardiovascular_phenotype|HCN4-related_disorder|Cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified|not_provided|Brugada_syndrome": 1,
    "Brugada_syndrome_8|HCN4-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8|HCN4-related_disorder": 1,
    "Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Brugada_syndrome_8|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Sick_sinus_syndrome_2|_autosomal_dominant": 1,
    "HCN4-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_8|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18|Sick_sinus_syndrome_2|_autosomal_dominant|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Brugada_syndrome_8|HCN4-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_8|Sick_sinus_syndrome_2|_autosomal_dominant|not_specified": 1,
    "Brugada_syndrome_8|Cardiovascular_phenotype|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Epilepsy|_idiopathic_generalized|_susceptibility_to|_18": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 1,
    "HCN4-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Sick_sinus_syndrome_2|_autosomal_dominant|Brugada_syndrome_8": 1,
    "REC114-related_disorder": 1,
    "not_provided|REC114-related_disorder": 1,
    "Oocyte_maturation_defect_10": 2,
    "REC114-related_disorder|not_provided": 2,
    "NPTN-related_neurodevelopmental_disorder": 6,
    "NPTN-related_neurodevelopmental_disorder|Developmental_disorder": 1,
    "LOXL1-related_disorder": 5,
    "Exfoliation_syndrome|_susceptibility_to": 2,
    "not_provided|LOXL1-related_disorder": 1,
    "LOXL1-related_disorder|Exfoliation_syndrome|_susceptibility_to": 1,
    "PML-related_disorder": 13,
    "PML-related_disorder|not_provided": 1,
    "not_provided|not_specified|PML-related_disorder": 1,
    "not_specified|PML-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_33": 288,
    "not_provided|Syndromic_Microphthalmia|_Recessive": 1,
    "Matthew-Wood_syndrome": 105,
    "not_provided|Matthew-Wood_syndrome": 14,
    "Syndromic_Microphthalmia|_Recessive|not_provided": 1,
    "Syndromic_Microphthalmia|_Recessive": 4,
    "Matthew-Wood_syndrome|not_provided": 14,
    "Matthew-Wood_syndrome|not_provided|STRA6-related_disorder": 2,
    "not_provided|Matthew-Wood_syndrome|STRA6-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Matthew-Wood_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Matthew-Wood_syndrome": 1,
    "STRA6-related_disorder": 7,
    "Inborn_genetic_diseases|Matthew-Wood_syndrome": 4,
    "Inborn_genetic_diseases|STRA6-related_disorder": 1,
    "STRA6-related_disorder|not_provided|Matthew-Wood_syndrome": 3,
    "Matthew-Wood_syndrome|Inborn_genetic_diseases": 4,
    "not_specified|STRA6-related_disorder|not_provided|Matthew-Wood_syndrome": 1,
    "not_provided|Matthew-Wood_syndrome|not_specified": 2,
    "Matthew-Wood_syndrome|Syndromic_Microphthalmia|_Recessive": 1,
    "not_specified|not_provided|Matthew-Wood_syndrome": 1,
    "not_provided|Matthew-Wood_syndrome|Inborn_genetic_diseases": 1,
    "STRA6-related_disorder|Inborn_genetic_diseases|Matthew-Wood_syndrome": 2,
    "Matthew-Wood_syndrome|not_provided|Microphthalmia|_isolated|_with_coloboma_8": 1,
    "not_provided|STRA6-related_disorder|Matthew-Wood_syndrome": 1,
    "STRA6-related_disorder|Matthew-Wood_syndrome": 2,
    "Matthew-Wood_syndrome|STRA6-related_disorder": 1,
    "Matthew-Wood_syndrome|STRA6-related_disorder|not_provided": 1,
    "CCDC33-related_disorder": 3,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency": 72,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|not_provided": 13,
    "not_provided|CYP11A1-related_disorder": 1,
    "not_provided|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency": 13,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|Inborn_genetic_diseases": 4,
    "CYP11A1-related_disorder": 2,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|not_provided|not_specified": 3,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|CYP11A1-related_disorder|not_specified|not_provided": 1,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|not_provided|CYP11A1-related_disorder": 3,
    "Congenital_Adrenal_Insufficiency": 1,
    "CYP11A1-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|not_specified|not_provided|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency|CYP11A1-related_disorder|Congenital_adrenal_hyperplasia": 1,
    "Inborn_genetic_diseases|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency": 4,
    "not_specified|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency": 2,
    "not_provided|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|Classic_congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency": 1,
    "CYP11A1-related_disorder|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|not_specified|not_provided": 1,
    "not_provided|Congenital_Adrenal_Insufficiency": 1,
    "not_provided|Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|CYP11A1-related_disorder": 1,
    "Congenital_adrenal_insufficiency_with_46|_XY_sex_reversal_OR_46|XY_disorder_of_sex_development-adrenal_insufficiency_due_to_CYP11A1_deficiency|not_specified": 1,
    "SEMA7A-related_disorder": 11,
    "John_Milton_Hagen_blood_group_system": 7,
    "not_specified|John_Milton_Hagen_blood_group_system": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_11": 1,
    "EDC3-related_disorder": 3,
    "not_specified|Intellectual_disability|_autosomal_recessive_50": 1,
    "not_provided|EDC3-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_50": 2,
    "CYP1A1-related_disorder|not_provided": 3,
    "CYP1A1-related_disorder": 12,
    "not_provided|CYP1A1-related_disorder": 1,
    "MPI-congenital_disorder_of_glycosylation": 477,
    "not_provided|MPI-congenital_disorder_of_glycosylation": 10,
    "MPI-related_disorder|MPI-congenital_disorder_of_glycosylation": 1,
    "MPI-related_disorder|not_specified|not_provided|MPI-congenital_disorder_of_glycosylation": 2,
    "not_specified|MPI-congenital_disorder_of_glycosylation": 4,
    "not_specified|not_provided|MPI-congenital_disorder_of_glycosylation|MPI-related_disorder": 1,
    "MPI-congenital_disorder_of_glycosylation|not_provided": 10,
    "MPI-related_disorder": 2,
    "MPI-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|MPI-congenital_disorder_of_glycosylation": 5,
    "Inborn_genetic_diseases|MPI-congenital_disorder_of_glycosylation": 2,
    "not_provided|MPI-congenital_disorder_of_glycosylation|not_specified": 2,
    "MPI-congenital_disorder_of_glycosylation|not_specified": 5,
    "not_provided|not_specified|MPI-congenital_disorder_of_glycosylation": 3,
    "MPI-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 4,
    "MPI-related_disorder|MPI-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_specified|MPI-congenital_disorder_of_glycosylation|MPI-related_disorder": 1,
    "MPI-related_disorder|not_provided|MPI-congenital_disorder_of_glycosylation": 1,
    "not_specified|MPI-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_specified|MPI-congenital_disorder_of_glycosylation|MPI-related_disorder|not_provided": 1,
    "MPI-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "MPI-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_20": 3,
    "COX5A-related_disorder|not_provided": 1,
    "SCAMP5-related_neurodevelopmental_disorder_with_autistic_features_and_seizures|Macrocephaly-developmental_delay_syndrome|Inborn_genetic_diseases|not_provided|Global_developmental_delay|SCAMP5-related_neurodevelopmental_and_movement_disorder": 1,
    "NEIL1-related_disorder": 7,
    "Congenital_disorder_of_deglycosylation_2": 17,
    "Congenital_disorder_of_deglycosylation_2|not_specified": 1,
    "MAN2C1-related_disorder|not_specified": 1,
    "not_specified|Congenital_disorder_of_deglycosylation_2": 2,
    "MAN2C1-related_disorder": 2,
    "Hypogonadotropic_hypogonadism_27_without_anosmia": 1,
    "SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation": 62,
    "not_provided|SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation": 8,
    "SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation|not_provided": 6,
    "not_specified|SIN3A-related_disorder|not_provided": 1,
    "SIN3A-related_disorder": 8,
    "SIN3A-related_intellectual_disability_syndrome": 3,
    "Inborn_genetic_diseases|SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation": 2,
    "SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation|Inborn_genetic_diseases": 1,
    "not_provided|SIN3A-related_disorder": 3,
    "SIN3A-related_disorder|not_provided": 7,
    "SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation|not_provided|Inborn_genetic_diseases": 2,
    "Chromosome_15q24_deletion_syndrome": 1,
    "SIN3A-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation|SIN3A-related_disorder|Intellectual_disability|not_provided": 1,
    "SIN3A-related_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "SIN3A-related_intellectual_disability_syndrome_due_to_a_point_mutation|not_provided|SIN3A-related_intellectual_disability_syndrome": 1,
    "not_specified|SNUPN_deficiency_muscular_dystrophy": 1,
    "Tayoun-Maawali_syndrome": 3,
    "Neurodevelopmental_disorder|not_specified|Tayoun-Maawali_syndrome": 1,
    "Glutaric_acidemia_type_2A|Multiple_acyl-CoA_dehydrogenase_deficiency": 8,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified|Glutaric_acidemia_IIa": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2A|not_specified": 1,
    "Glutaric_acidemia_type_2A": 14,
    "ETFA-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency": 3,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2A": 6,
    "ETFA-related_disorder|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided|Glutaric_acidemia_IIa": 1,
    "ETFA-related_disorder|Inborn_genetic_diseases|not_provided|Glutaric_acidemia_IIa|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Glutaric_acidemia_type_2A|Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency": 2,
    "not_specified|Glutaric_acidemia_type_2A": 1,
    "ETFA-related_disorder": 2,
    "Glutaric_acidemia_type_2A|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "ETFA-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "Glutaric_acidemia_IIa|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_type_2A|not_provided": 1,
    "Glutaric_acidemia_type_2A|not_provided|not_specified|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|Glutaric_acidemia_IIa": 1,
    "Glutaric_acidemia_type_2A|not_provided": 1,
    "Glutaric_acidemia_type_2A|not_specified|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|ETFA-related_disorder": 1,
    "Glutaric_acidemia_type_2A|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "SCAPER-related_disorder|Inborn_genetic_diseases": 3,
    "Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP": 25,
    "SCAPER-related_disorder": 46,
    "SCAPER-related_disorder|not_provided": 13,
    "Inborn_genetic_diseases|SCAPER-related_disorder|not_provided": 1,
    "SCAPER-related_disorder|Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|not_provided": 2,
    "Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|Intellectual_disability|_moderate|Rod-cone_dystrophy": 2,
    "SCAPER-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Optic_atrophy|SCAPER-related_disorder": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|SCAPER-related_disorder": 1,
    "not_provided|SCAPER-related_disorder": 7,
    "Bardet-Biedl_syndrome_1|Retinal_dystrophy": 1,
    "SCAPER-related_disorder|Retinal_dystrophy": 2,
    "Inborn_genetic_diseases|SCAPER-related_disorder": 8,
    "Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|not_provided": 2,
    "Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|Attention_deficit_hyperactivity_disorder|Intellectual_disability|_moderate|Rod-cone_dystrophy": 1,
    "Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|SCAPER-related_disorder": 1,
    "Brachydactyly|Abnormal_speech_pattern|Pigmentary_retinopathy|Obesity|Short_stature|Intellectual_disability": 1,
    "SCAPER-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP": 4,
    "SCAPER-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa|Syndromic_retinitis_pigmentosa|Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP": 1,
    "Retinal_dystrophy|SCAPER-related_disorder": 2,
    "SCAPER-related_disorder|Optic_atrophy": 1,
    "not_provided|Intellectual_developmental_disorder_and_retinitis_pigmentosa%3B_IDDRP|SCAPER-related_disorder": 3,
    "PSTPIP1-related_disorder": 8,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 435,
    "Autoinflammatory_syndrome|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 7,
    "not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 34,
    "PSTPIP1-related_disorder|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 3,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Hyperzincemia_and_hypercalprotectinemia": 2,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome": 12,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Inborn_genetic_diseases": 13,
    "not_provided|not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 4,
    "Inborn_genetic_diseases|not_provided|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "not_provided|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 2,
    "PSTPIP1-related_disorder|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided": 13,
    "not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 9,
    "Autoinflammatory_syndrome|not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 14,
    "not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome|Behcet_disease": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome|not_specified|not_provided": 2,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified|not_provided": 4,
    "Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided": 1,
    "not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Inborn_genetic_diseases": 1,
    "Behcet_disease|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "not_provided|PSTPIP1-related_disorder|Inborn_genetic_diseases|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "not_specified|PSTPIP1-related_disorder|Autoinflammatory_syndrome|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome|not_provided": 3,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided|not_specified": 1,
    "Hyperzincemia_and_hypercalprotectinemia|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 6,
    "Autoinflammatory_syndrome|not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified": 3,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified": 10,
    "Autoinflammatory_syndrome|not_specified|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 2,
    "Inborn_genetic_diseases|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome": 1,
    "not_provided|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified": 3,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified|PSTPIP1-related_disorder": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "PSTPIP1-related_disorder|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 2,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|PSTPIP1-related_disorder|not_specified": 1,
    "not_provided|Hyperzincemia_and_hypercalprotectinemia|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "Hyperzincemia_and_hypercalprotectinemia": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|PSTPIP1-related_disorder|not_provided": 1,
    "not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Inborn_genetic_diseases": 3,
    "Autoinflammatory_syndrome|not_provided|not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 2,
    "not_specified|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 2,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|PSTPIP1-related_disorder|not_specified|not_provided": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome|not_specified": 2,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|PSTPIP1-related_disorder|Autoinflammatory_syndrome": 1,
    "not_specified|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|PSTPIP1-related_disorder|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "not_specified|not_provided|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|not_provided|Autoinflammatory_syndrome": 1,
    "Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|PSTPIP1-related_disorder": 1,
    "not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome|Autoinflammatory_syndrome": 1,
    "not_provided|not_specified|Autoinflammatory_syndrome|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "PSTPIP1-related_disorder|Autoinflammatory_syndrome|not_provided|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|Pyogenic_arthritis-pyoderma_gangrenosum-acne_syndrome": 1,
    "PEAK1-related_disorder": 20,
    "HMG20A-related_disorder": 2,
    "not_provided|LINGO1-related_disorder": 2,
    "Intellectual_disability|_autosomal_recessive_64|not_specified": 1,
    "LINGO1-related_disorder": 11,
    "LINGO1-related_disorder|not_provided": 3,
    "Intellectual_disability|_autosomal_recessive_64": 6,
    "not_provided|Intellectual_disability|_autosomal_recessive_64": 2,
    "not_specified|Intellectual_disability|_autosomal_recessive_64": 2,
    "Intellectual_disability|_autosomal_recessive_64|not_provided": 2,
    "Neurodevelopmental_disorder_with_seizures_and_gingival_overgrowth|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_seizures_and_gingival_overgrowth": 12,
    "TBC1D2B-related_disorder": 4,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_seizures_and_gingival_overgrowth": 1,
    "Usher_syndrome|Childhood_onset_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_48|not_provided|Usher_syndrome_type_1J|Hearing_loss|_autosomal_recessive|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_48": 11,
    "not_provided|not_specified|CIB2-related_disorder": 1,
    "Usher_syndrome_type_1J": 1,
    "CIB2-related_disorder|not_specified|not_provided": 1,
    "Usher_syndrome_type_1J|Autosomal_recessive_nonsyndromic_hearing_loss_48|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_48|Usher_syndrome_type_1J": 1,
    "not_provided|CIB2-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_48|Usher_syndrome_type_1J|not_provided": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_48|Usher_syndrome_type_1J": 1,
    "CIB2-related_disorder|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_48|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_48|Hearing_loss|_autosomal_recessive|Usher_syndrome_type_1J": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_48": 1,
    "CIB2-related_disorder": 2,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_48|Usher_syndrome_type_1J|not_provided|Retinal_dystrophy": 1,
    "Usher_syndrome_type_1J|Usher_syndrome_type_1": 1,
    "Retinitis_pigmentosa_90|not_provided": 3,
    "not_provided|Retinitis_pigmentosa_90": 1,
    "not_provided|IDH3A-related_disorder": 2,
    "Retinitis_pigmentosa_90": 5,
    "IDH3A-related_disorder|not_provided": 6,
    "IDH3A-related_disorder": 1,
    "Retinitis_pigmentosa_90|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|not_specified|Retinitis_pigmentosa_90": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_90|not_provided": 1,
    "Neurodegeneration|_early-onset|_with_choreoathetoid_movements_and_microcytic_anemia": 4,
    "not_provided|IREB2-related_disorder": 5,
    "IREB2-related_disorder|not_provided": 2,
    "Neurodegeneration|_early-onset|_with_choreoathetoid_movements_and_microcytic_anemia|not_provided": 5,
    "Neurodegeneration|_early-onset|_with_choreoathetoid_movements_and_microcytic_anemia|NEURODEGENERATION|_EARLY-ONSET|_WITH_CHOREOATHETOSIS_AND_MICROCYTIC_ANEMIA": 2,
    "NEURODEGENERATION|_EARLY-ONSET|_WITH_CHOREOATHETOSIS_AND_MICROCYTIC_ANEMIA|Neurodegeneration|_early-onset|_with_choreoathetoid_movements_and_microcytic_anemia": 2,
    "Neurodegeneration|_early-onset|_with_choreoathetoid_movements_and_microcytic_anemia|IREB2-related_disorder|not_provided": 1,
    "SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|not_provided": 1,
    "CHRNA5-related_condition": 1,
    "nicotine_response_-_Toxicity|Lung_cancer_susceptibility_2|Susceptibility_to_severe_coronavirus_disease_(COVID-19)_due_to_high_levels_of_fibrinogen_and_C-reactive_protein|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3": 1,
    "Urinary_bladder|_atony_of|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|not_provided": 4,
    "Inborn_genetic_diseases|Urinary_bladder|_atony_of|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3": 3,
    "SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Urinary_bladder|_atony_of": 51,
    "Urinary_bladder|_atony_of|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Inborn_genetic_diseases": 2,
    "not_provided|CHRNA3-related_disorder": 1,
    "SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Urinary_bladder|_atony_of|Inborn_genetic_diseases": 2,
    "Urinary_bladder|_atony_of|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3": 1,
    "Urinary_bladder|_atony_of": 5,
    "not_provided|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Urinary_bladder|_atony_of|Inborn_genetic_diseases": 1,
    "SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Urinary_bladder|_atony_of|not_provided|CHRNA3-related_disorder": 1,
    "not_provided|Urinary_bladder|_atony_of|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3": 1,
    "SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Urinary_bladder|_atony_of|CHRNA3-related_disorder": 1,
    "not_provided|SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Lung_cancer_susceptibility_2": 1,
    "CHRNA3-related_disorder": 2,
    "SMOKING_AS_A_QUANTITATIVE_TRAIT_LOCUS_3|Urinary_bladder|_atony_of|not_provided": 1,
    "Urinary_bladder|_atony_of|not_provided": 3,
    "not_provided|Urinary_bladder|_atony_of": 2,
    "not_provided|Urinary_bladder|_atony_of|not_specified": 1,
    "CTSH-related_disorder": 2,
    "MIR184-related_disorder|Developmental_cataract": 1,
    "EDICT_syndrome": 1,
    "TMED3-related_disorder": 6,
    "Neurodevelopmental_disorder_with_microcephaly|_epilepsy|_and_hypomyelination": 5,
    "Neurodevelopmental_disorder_with_microcephaly|_epilepsy|_and_hypomyelination|not_provided": 2,
    "MTHFS-related_disorder|not_provided": 3,
    "not_provided|MTHFS-related_disorder": 2,
    "Tyrosinemia_type_I|not_provided|Hypertyrosinemia": 1,
    "Tyrosinemia_type_I": 607,
    "Tyrosinemia_type_I|not_provided": 24,
    "not_provided|Tyrosinemia_type_I": 25,
    "FAH-related_disorder|Tyrosinemia_type_I|not_specified": 2,
    "Tyrosinemia_type_I|not_specified|not_provided": 3,
    "not_provided|Tyrosinemia|See_cases|Tyrosinemia_type_I": 1,
    "Tyrosinemia_type_I|not_specified": 8,
    "not_specified|Tyrosinemia_type_I": 6,
    "not_provided|not_specified|Tyrosinemia_type_I": 3,
    "not_provided|Tyrosinemia_type_I|not_specified": 3,
    "Inborn_genetic_diseases|Tyrosinemia_type_I": 11,
    "not_specified|not_provided|Tyrosinemia_type_I": 4,
    "Tyrosinemia_type_I|Inborn_genetic_diseases": 5,
    "Tyrosinemia_type_I|not_provided|not_specified": 2,
    "T-substance_anomaly|not_provided|Tyrosinemia_type_I|Tyrosinemia_type_II": 1,
    "Tyrosinemia_type_I|not_provided|FAH-related_disorder": 1,
    "not_specified|Tyrosinemia_type_I|not_provided": 5,
    "Tyrosinemia_type_I|not_provided|FAH-related_disorder|Inborn_genetic_diseases": 1,
    "FAH-related_disorder|Hypertyrosinemia|not_specified|Tyrosinemia_type_I": 1,
    "Tyrosinemia_type_I|FAH-related_disorder": 6,
    "FAH-related_disorder|Tyrosinemia_type_I": 12,
    "FAH-related_disorder": 4,
    "FAH-related_disorder|not_provided|Tyrosinemia_type_I": 4,
    "not_specified|Tyrosinemia_type_I|FAH-related_disorder": 4,
    "not_specified|Tyrosinemia_type_I|not_provided|FAH-related_disorder": 1,
    "Tyrosinemia": 1,
    "Tyrosinemia_type_I|not_specified|not_provided|FAH-related_disorder": 1,
    "not_provided|Tyrosinemia_type_I|Inborn_genetic_diseases": 1,
    "Tyrosinemia_type_I|not_specified|FAH-related_disorder": 1,
    "FAH-related_disorder|not_specified|not_provided|Tyrosinemia_type_I": 2,
    "FAH-related_disorder|Tyrosinemia_type_I|not_provided": 2,
    "FAH-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Tyrosinemia_type_I|FAH-related_disorder": 1,
    "Tyrosinemia_type_I|Beta-D-mannosidosis": 1,
    "not_provided|not_specified|Tyrosinemia_type_I|Fumarylacetoacetase_pseudodeficiency": 1,
    "Inborn_genetic_diseases|Tyrosinemia_type_I|not_provided": 2,
    "Tyrosinemia_type_I|Inborn_genetic_diseases|not_provided": 1,
    "FAH-related_disorder|Inborn_genetic_diseases|not_provided|Tyrosinemia_type_I|Tyrosinemia": 1,
    "Tyrosinemia_type_I|FAH-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Tyrosinemia_type_I|not_provided|FAH-related_disorder": 1,
    "not_provided|not_specified|Tyrosinemia_type_I|FAH-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|FAH-related_disorder": 1,
    "not_provided|Hypertyrosinemia": 2,
    "Webb-Dattani_syndrome": 7,
    "Webb-Dattani_syndrome|not_provided": 4,
    "ARNT2-related_disorder": 2,
    "not_provided|ARNT2-related_disorder": 2,
    "ARNT2-related_disorder|not_provided": 3,
    "not_provided|not_specified|Webb-Dattani_syndrome": 1,
    "Webb-Dattani_syndrome|not_specified|not_provided": 1,
    "not_provided|Webb-Dattani_syndrome": 2,
    "ARNT2-related_disorder|not_provided|Webb-Dattani_syndrome": 1,
    "CEMIP-related_disorder": 11,
    "CEMIP-related_disorder|not_provided": 6,
    "not_provided|CEMIP-related_disorder": 1,
    "CEMIP-related_disorder|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta|_type_20": 4,
    "not_provided|Osteogenesis_imperfecta|_type_20": 1,
    "MESD-related_disorder|not_provided": 3,
    "Shwachman_syndrome|Shwachman-Diamond_syndrome_2|not_provided": 1,
    "Shwachman-Diamond_syndrome_2": 8,
    "Shwachman-Diamond_syndrome_2|Shwachman_syndrome": 4,
    "not_provided|EFL1-related_disorder": 11,
    "not_provided|Shwachman-Diamond_syndrome_2": 4,
    "EFL1-related_disorder|not_provided": 10,
    "Shwachman_syndrome|not_provided": 1,
    "Shwachman-Diamond_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Shwachman_syndrome|Shwachman-Diamond_syndrome_2": 3,
    "Inborn_genetic_diseases|Shwachman-Diamond_syndrome_2": 1,
    "Shwachman-Diamond_syndrome_2|not_provided": 5,
    "EFL1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Immunodeficiency": 5,
    "Inborn_genetic_diseases|Shwachman_syndrome|not_specified|not_provided": 1,
    "EFL1-related_disorder": 2,
    "Shwachman_syndrome|EFL1-related_disorder": 2,
    "not_specified|not_provided|EFL1-related_disorder": 1,
    "Diamond-Blackfan_anemia_4": 15,
    "Diamond-Blackfan_anemia_4|not_provided|not_specified": 1,
    "Diamond-Blackfan_anemia_4|not_provided|Diamond-Blackfan_anemia": 1,
    "RPS17-related_condition": 1,
    "Diamond-Blackfan_anemia_4|Diamond-Blackfan_anemia": 1,
    "Developmental_and_epileptic_encephalopathy|_48|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_48": 10,
    "not_provided|AP3B2-related_disorder": 7,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_48": 1,
    "Developmental_and_epileptic_encephalopathy|_48|not_provided": 11,
    "Developmental_and_epileptic_encephalopathy|_48|not_provided|Inborn_genetic_diseases": 1,
    "AP3B2-related_disorder|not_provided": 13,
    "Developmental_and_epileptic_encephalopathy|_48": 17,
    "AP3B2-related_disorder": 3,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|not_specified|AP3B2-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_48|Epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|not_provided|AP3B2-related_disorder": 1,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_48": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_48|Delayed_speech_and_language_development|Generalized_hypotonia|Hypotonia|Abnormality_of_eye_movement|Gastroesophageal_reflux|Abnormal_speech_pattern|Autism|Microcephaly|Global_developmental_delay|Feeding_difficulties": 1,
    "not_provided|AP3B2-related_disorder|Intellectual_disability": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_48|AP3B2-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_68": 8,
    "not_provided|HOMER2-related_disorder": 1,
    "HOMER2-related_disorder|not_provided": 2,
    "HOMER2-related_disorder": 8,
    "not_provided|HOMER2-related_disorder|not_specified": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_68": 1,
    "HOMER2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "HOMER2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|HOMER2-related_disorder": 2,
    "not_specified|HOMER2-related_disorder|not_provided": 1,
    "Premature_ovarian_failure_16": 4,
    "46_XX_gonadal_dysgenesis": 2,
    "Premature_ovarian_failure_16|not_specified": 1,
    "not_provided|Galloway-Mowat_syndrome_1|WDR73-related_disorder": 1,
    "Inborn_genetic_diseases|Galloway-Mowat_syndrome_1|not_provided": 4,
    "Galloway-Mowat_syndrome_1|not_specified|not_provided": 2,
    "not_provided|Galloway-Mowat_syndrome_1": 9,
    "Galloway-Mowat_syndrome_1": 66,
    "Inborn_genetic_diseases|WDR73-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Galloway-Mowat_syndrome_1": 1,
    "Galloway-Mowat_syndrome_1|not_provided": 17,
    "WDR73-related_disorder": 3,
    "WDR73-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|Galloway-Mowat_syndrome_1": 4,
    "Galloway-Mowat_syndrome_1|Inborn_genetic_diseases|not_provided": 4,
    "Galloway-Mowat_syndrome_1|Nephrotic_syndrome|not_provided": 2,
    "not_provided|WDR73-related_disorder": 2,
    "Galloway-Mowat_syndrome_1|not_provided|WDR73-related_disorder": 1,
    "not_specified|Galloway-Mowat_syndrome_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Galloway-Mowat_syndrome_1": 2,
    "Galloway-Mowat_syndrome_1|Inborn_genetic_diseases": 7,
    "Galloway-Mowat_syndrome_1|Nephrotic_syndrome": 1,
    "not_provided|Galloway-Mowat_syndrome_1|Inborn_genetic_diseases": 2,
    "not_provided|Galloway-Mowat_syndrome_1|not_specified": 1,
    "not_provided|WDR73-related_disorder|Galloway-Mowat_syndrome_1": 1,
    "Seizure|Dyskinesia": 1,
    "ZNF592-related_disorder": 9,
    "not_provided|not_specified|Galloway-Mowat_syndrome_1": 1,
    "not_specified|not_provided|Galloway-Mowat_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|ALPK3-related_disorder": 3,
    "not_provided|Cardiovascular_phenotype|not_specified|ALPK3-related_disorder": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_hypertrophic_27": 7,
    "Cardiovascular_phenotype|not_provided|ALPK3-related_disorder|not_specified": 2,
    "not_provided|ALPK3-related_disorder|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_hypertrophic_27|not_specified": 2,
    "ALPK3-related_disorder|Cardiovascular_phenotype|not_provided": 4,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27|not_provided": 11,
    "Cardiomyopathy|_familial_hypertrophic_27": 38,
    "ALPK3-related_disorder|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27": 4,
    "ALPK3-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 5,
    "Cardiovascular_phenotype|not_specified|not_provided|ALPK3-related_disorder": 3,
    "ALPK3-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|not_provided": 6,
    "not_provided|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype": 11,
    "not_provided|ALPK3-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "not_provided|Cardiovascular_phenotype|ALPK3-related_disorder": 4,
    "Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_provided": 11,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27": 3,
    "ALPK3-related_disorder": 7,
    "ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "ALPK3-related_disorder|not_provided|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|not_specified|not_provided": 1,
    "not_specified|ALPK3-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|_familial_hypertrophic_27": 2,
    "not_provided|not_specified|Cardiovascular_phenotype|ALPK3-related_disorder": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|ALPK3-related_disorder|not_provided|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiovascular_phenotype|not_specified|ALPK3-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|ALPK3-related_disorder": 1,
    "ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|not_provided|Cardiovascular_phenotype": 1,
    "ALPK3-related_disorder|not_provided|not_specified|Cardiovascular_phenotype": 2,
    "ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "ALPK3-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "ALPK3-related_disorder|not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiovascular_phenotype|not_provided|ALPK3-related_disorder|Cardiomyopathy": 1,
    "pediatric-onset_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "ALPK3-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 2,
    "Cardiomyopathy|_familial_hypertrophic_27|ALPK3-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "not_provided|ALPK3-related_disorder|not_specified|Cardiovascular_phenotype": 3,
    "not_specified|not_provided|ALPK3-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|not_provided|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|ALPK3-related_disorder|not_specified|not_provided": 2,
    "not_provided|ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_specified": 3,
    "not_specified|ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|ALPK3-related_disorder|not_provided": 1,
    "ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_provided|Neurodevelopmental_disorder": 1,
    "ALPK3-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 5,
    "Cardiomyopathy|_familial_hypertrophic_27|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27|not_specified": 1,
    "not_provided|Cardiomyopathy|_familial_hypertrophic_27|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|_familial_hypertrophic_27|not_specified|Cardiovascular_phenotype": 1,
    "Abnormality_of_the_cardiovascular_system": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|ALPK3-related_disorder": 1,
    "ALPK3-related_disorder|Cardiomyopathy|_familial_hypertrophic_27|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|Neurodevelopmental_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic_27|not_provided|not_specified": 1,
    "ALPK3-related_disorder|not_provided": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|Cardiovascular_phenotype": 1,
    "not_provided|ALPK3-related_disorder": 1,
    "Cardiomyopathy|_familial_hypertrophic_27|ALPK3-related_disorder": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|ALPK3-related_disorder": 1,
    "ALPK3-related_disorder|not_provided|not_specified": 1,
    "SLC28A1-related_disorder|not_provided": 1,
    "SLC28A1-related_disorder": 23,
    "not_provided|SLC28A1-related_disorder": 2,
    "Uridine-cytidineuria": 2,
    "SLC28A1-related_disorder|Uridine-cytidineuria": 1,
    "Uridine-cytidineuria|SLC28A1-related_disorder|not_provided": 1,
    "AKAP13-related_disorder": 1,
    "AGBL1-related_disorder": 17,
    "Corneal_dystrophy|_Fuchs_endothelial|_8": 6,
    "AGBL1-related_disorder|Fuchs'_endothelial_dystrophy": 1,
    "not_specified|Corneal_dystrophy|_Fuchs_endothelial|_8": 1,
    "Fuchs'_endothelial_dystrophy": 1,
    "Fuchs'_endothelial_dystrophy|Corneal_dystrophy|_Fuchs_endothelial|_8|not_provided": 1,
    "AGBL1-related_disorder|not_specified": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_8|Fuchs'_endothelial_dystrophy|AGBL1-related_disorder": 1,
    "not_provided|AGBL1-related_disorder": 1,
    "NTRK3-related_disorder": 10,
    "not_provided|NTRK3-related_disorder": 6,
    "Entrectinib_resistance": 1,
    "Entrectinib_resistance|Cabozantinib_resistance|Repotrectinib_resistance|Selitrectinib_resistance|Larotrectinib_resistance": 1,
    "NTRK3-related_disorder|not_provided": 1,
    "not_specified|Neonatal_cardiomyopathy": 1,
    "Osteochondritis_dissecans": 21,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 41,
    "ACAN-related_disorder": 12,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 11,
    "ACAN-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_specified|not_provided|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 2,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|not_specified|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 1,
    "Short_stature_and_advanced_bone_age|_with_early-onset_osteoarthritis": 2,
    "not_specified|ACAN-related_disorder|Inborn_genetic_diseases|not_provided|Osteochondritis_dissecans": 1,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 2,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|not_provided": 1,
    "Short_stature_and_advanced_bone_age": 4,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|not_specified|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 3,
    "Inborn_genetic_diseases|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 1,
    "not_provided|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 4,
    "ACAN-related_disorder|not_provided": 10,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 3,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_specified|not_provided": 1,
    "not_provided|Osteochondritis_dissecans|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "not_specified|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 1,
    "not_provided|ACAN-related_disorder": 7,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|ACAN-related_disorder": 1,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided": 3,
    "Osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_provided": 3,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Osteochondritis_dissecans|not_provided": 1,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Meniere_disease": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided": 4,
    "Osteochondritis_dissecans|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Osteochondritis_dissecans": 1,
    "not_specified|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_provided": 2,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided": 1,
    "not_provided|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 3,
    "Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_specified|not_provided": 1,
    "not_provided|Short_stature_and_advanced_bone_age|_with_early-onset_osteoarthritis": 1,
    "not_provided|Osteochondritis_dissecans": 2,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type|not_specified|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 2,
    "ACAN-related_disorder|not_specified|not_provided": 1,
    "not_specified|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Inborn_genetic_diseases": 1,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 2,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Osteochondritis_dissecans": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 4,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type": 3,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_provided": 2,
    "not_specified|not_provided|Osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "not_provided|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_specified|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_specified|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_provided": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "not_provided|not_specified|Meniere_disease": 1,
    "Osteochondritis_dissecans|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|ACAN-related_disorder": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_specified|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_provided": 2,
    "not_provided|Osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 2,
    "Inborn_genetic_diseases|Osteochondritis_dissecans": 2,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 2,
    "not_provided|Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 1,
    "Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_specified|not_provided": 2,
    "not_provided|Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 3,
    "not_provided|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 1,
    "not_specified|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "not_specified|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans": 1,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type|not_provided": 1,
    "not_provided|Osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_specified": 1,
    "not_provided|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "Osteochondritis_dissecans|Inborn_genetic_diseases": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Inborn_genetic_diseases": 1,
    "Osteochondritis_dissecans|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type": 2,
    "not_provided|ACAN-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Meniere_disease": 1,
    "Inborn_genetic_diseases|ACAN-related_disorder": 1,
    "not_provided|not_specified|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 1,
    "Inborn_genetic_diseases|not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Spondyloepiphyseal_dysplasia|_Kimberley_type": 1,
    "Short_stature-advanced_bone_age-early-onset_osteoarthritis_syndrome": 1,
    "Spondyloepiphyseal_dysplasia|_Kimberley_type|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|ACAN-related_disorder|not_provided": 1,
    "not_provided|not_specified|Spondyloepimetaphyseal_dysplasia|_aggrecan_type": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|not_provided": 1,
    "Short_stature_and_advanced_bone_age|_with_early-onset_osteoarthritis|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Osteochondritis_dissecans": 1,
    "Short_stature_and_advanced_bone_age|_with_or_without_early-onset_osteoarthritis_and/or_osteochondritis_dissecans|not_provided|Osteochondritis_dissecans": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_aggrecan_type|not_specified": 1,
    "Spondyloepimetaphyseal_dysplasia|_aggrecan_type|Osteochondritis_dissecans|Spondyloepiphyseal_dysplasia|_Kimberley_type|not_specified|not_provided": 1,
    "Retinitis_pigmentosa|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy": 15,
    "Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 4,
    "Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided": 6,
    "Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa": 2,
    "not_specified|not_provided|Retinitis_pigmentosa|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy": 1,
    "Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Retinal_dystrophy|Retinitis_Pigmentosa|_Recessive|not_provided": 1,
    "Newfoundland_cone-rod_dystrophy|Bothnia_retinal_dystrophy|Pigmentary_retinal_dystrophy|not_provided": 1,
    "not_provided|RLBP1-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|not_provided": 8,
    "not_provided|RLBP1-related_disorder": 2,
    "Retinitis_pigmentosa|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|RLBP1-related_disorder|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 1,
    "Pigmentary_retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Bothnia_retinal_dystrophy|Retinitis_punctata_albescens|RLBP1-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "Bothnia_retinal_dystrophy": 5,
    "not_provided|Pigmentary_retinal_dystrophy|Bothnia_retinal_dystrophy|not_specified": 1,
    "RLBP1-related_disorder|Retinal_disorders|Retinitis_punctata_albescens|Bothnia_retinal_dystrophy|Retinal_dystrophy|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|not_provided|Bothnia_retinal_dystrophy": 1,
    "Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Pigmentary_retinal_dystrophy|Bothnia_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided": 1,
    "Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|Retinal_dystrophy|Retinitis_pigmentosa|not_specified|not_provided|RLBP1-related_disorder": 1,
    "RLBP1-related_disorder|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy": 152,
    "Bothnia_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|not_provided": 1,
    "RLBP1-related_disorder": 1,
    "Pigmentary_retinal_dystrophy|Bothnia_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_punctata_albescens|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_Pigmentosa|_Recessive|not_specified|not_provided|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 1,
    "not_specified|not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 1,
    "not_provided|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|Bothnia_retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_punctata_albescens|Abnormality_of_the_eye|not_provided|Retinitis_pigmentosa|Bothnia_retinal_dystrophy|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|Bothnia_retinal_dystrophy|not_provided": 1,
    "Bothnia_retinal_dystrophy|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 1,
    "RLBP1-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_provided|Bothnia_retinal_dystrophy|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided": 1,
    "not_specified|Retinitis_pigmentosa|not_provided|Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy": 1,
    "Newfoundland_cone-rod_dystrophy|Bothnia_retinal_dystrophy|Pigmentary_retinal_dystrophy|RLBP1-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Newfoundland_cone-rod_dystrophy|Retinitis_punctata_albescens": 1,
    "Newfoundland_cone-rod_dystrophy|Pigmentary_retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_punctata_albescens|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|not_specified|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided": 1,
    "not_provided|Newfoundland_cone-rod_dystrophy|Bothnia_retinal_dystrophy|Pigmentary_retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Bothnia_retinal_dystrophy|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy|not_provided": 1,
    "RLBP1-related_disorder|not_specified|not_provided": 1,
    "Retinitis_Pigmentosa|_Recessive|Pigmentary_retinal_dystrophy|Newfoundland_cone-rod_dystrophy": 2,
    "Fanconi_anemia_complementation_group_I": 217,
    "FANCI-related_disorder": 4,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia": 103,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I": 134,
    "not_specified|Fanconi_anemia_complementation_group_I|Fanconi_anemia": 4,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_specified|not_provided": 5,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 12,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_I|Fanconi_anemia": 4,
    "not_provided|Fanconi_anemia_complementation_group_I": 3,
    "not_specified|Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia_complementation_group_I|Inborn_genetic_diseases": 5,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_I": 5,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 4,
    "FANCI-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 2,
    "not_provided|Fanconi_anemia_complementation_group_I|not_specified": 1,
    "not_specified|Microcephaly|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_I|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 7,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 4,
    "Fanconi_anemia_complementation_group_I|not_specified|Fanconi_anemia": 2,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I|FANCI-related_disorder": 1,
    "FANCI-related_disorder|Fanconi_anemia_complementation_group_I|Fanconi_anemia": 3,
    "FANCI-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 2,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_provided|not_specified": 2,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|Inborn_genetic_diseases|not_specified": 1,
    "FANCI-related_disorder|Fanconi_anemia": 4,
    "not_provided|Fanconi_anemia_complementation_group_I|Fanconi_anemia": 6,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_I": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_I|not_provided": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_provided": 14,
    "Fanconi_anemia|FANCI-related_disorder": 5,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_I": 3,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|not_provided": 5,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_I|not_provided": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|FANCI-related_disorder|not_provided": 1,
    "Fanconi_anemia_complementation_group_I|not_provided|not_specified|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_I": 1,
    "not_specified|Fanconi_anemia|Inborn_genetic_diseases": 3,
    "not_specified|FANCI-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia_complementation_group_I|not_specified": 2,
    "not_provided|Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_specified": 2,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|FANCI-related_disorder": 2,
    "Fanconi_anemia_complementation_group_I|not_provided|Fanconi_anemia": 4,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|Gastric_cancer": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_I": 8,
    "Fanconi_anemia_complementation_group_I|not_provided|Fanconi_anemia|FANCI-related_disorder|not_specified": 1,
    "not_provided|Fanconi_anemia_complementation_group_I|Fanconi_anemia|FANCI-related_disorder": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 2,
    "Fanconi_anemia_complementation_group_I|not_specified|not_provided|Fanconi_anemia": 1,
    "FANCI-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 1,
    "not_specified|Fanconi_anemia_complementation_group_I|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|Inborn_genetic_diseases": 4,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|not_specified|not_provided": 1,
    "not_specified|Fanconi_anemia|not_provided|FANCI-related_disorder|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|not_specified": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|Colorectal_cancer": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_I|Fanconi_anemia": 1,
    "Fanconi_anemia|not_specified|FANCI-related_disorder|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|FANCI-related_disorder": 2,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_provided|FANCI-related_disorder": 1,
    "Fanconi_anemia_complementation_group_I|Inborn_genetic_diseases|Fanconi_anemia": 2,
    "Immunodeficiency_62|Fanconi_anemia_complementation_group_I": 1,
    "FANCI-related_disorder|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_I|Immunodeficiency_62": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_I|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_I|FANCI-related_disorder": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_I|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_I|FANCI-related_disorder|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_I": 1,
    "Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|POLG-Related_Spectrum_Disorders|not_provided": 2,
    "FANCI-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_I|FANCI-related_disorder|not_specified": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_I|not_specified": 1,
    "not_specified|Fanconi_anemia_complementation_group_I|Fanconi_anemia|not_provided|POLG-Related_Spectrum_Disorders": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia|POLG-Related_Spectrum_Disorders": 2,
    "POLG-Related_Spectrum_Disorders": 11,
    "POLG-Related_Spectrum_Disorders|Mitochondrial_disease": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|POLG-Related_Spectrum_Disorders|Mitochondrial_disease": 1,
    "Fanconi_anemia_complementation_group_I|POLG-Related_Spectrum_Disorders|Mitochondrial_disease": 1,
    "POLG-Related_Spectrum_Disorders|Fanconi_anemia_complementation_group_I": 2,
    "not_provided|Fanconi_anemia|POLG-Related_Spectrum_Disorders|not_specified": 1,
    "Fanconi_anemia_complementation_group_I|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|POLG-Related_Spectrum_Disorders": 1,
    "POLG-related_disorder|POLG-Related_Spectrum_Disorders|Fanconi_anemia_complementation_group_I": 1,
    "POLG-related_disorder": 18,
    "Fanconi_anemia_complementation_group_I|POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy": 1789,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|not_specified|not_provided|Hereditary_spastic_paraplegia|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 1,
    "not_provided|Fanconi_anemia_complementation_group_I|Progressive_sclerosing_poliodystrophy": 1,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders": 1,
    "Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "Progressive_sclerosing_poliodystrophy|not_provided": 137,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "POLG-related_disorder|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder": 12,
    "not_specified|POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided|Fanconi_anemia_complementation_group_I": 1,
    "Progressive_sclerosing_poliodystrophy|not_specified": 43,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 24,
    "not_provided|not_specified|Progressive_sclerosing_poliodystrophy|Fanconi_anemia_complementation_group_I": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy": 38,
    "Fanconi_anemia_complementation_group_I|Fanconi_anemia|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Fanconi_anemia|POLG-Related_Spectrum_Disorders|Fanconi_anemia_complementation_group_I": 1,
    "Fanconi_anemia|POLG-Related_Spectrum_Disorders|not_provided|Fanconi_anemia_complementation_group_I": 1,
    "POLG-Related_Spectrum_Disorders|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 1,
    "not_provided|POLG-Related_Spectrum_Disorders|Fanconi_anemia|Fanconi_anemia_complementation_group_I": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 19,
    "Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|not_provided": 6,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 2,
    "POLG-related_disorder|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|not_provided": 2,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|not_provided": 8,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_provided|not_specified|Hereditary_spastic_paraplegia|Mitochondrial_disease|Progressive_sclerosing_poliodystrophy": 1,
    "not_specified|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 6,
    "Mitochondrial_disease|not_provided|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_disease": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "not_specified|Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|Mitochondrial_disease|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "POLG-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|not_specified": 4,
    "Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|POLG-related_disorder|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided|Mitochondrial_disease": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_provided": 1,
    "POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy": 8,
    "Progressive_sclerosing_poliodystrophy|not_specified|not_provided": 6,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 2,
    "POLG-Related_Spectrum_Disorders|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_disease|Progressive_sclerosing_poliodystrophy": 1,
    "Alpers-like_hepatocerebral_syndrome": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy|POLG-related_disorder": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 15,
    "POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "POLG-related_disorder|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 9,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 3,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 4,
    "Progressive_sclerosing_poliodystrophy|not_specified|Hereditary_spastic_paraplegia": 1,
    "Progressive_sclerosing_poliodystrophy|not_specified|Mitochondrial_disease": 1,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_disease": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy|not_provided": 6,
    "POLG-Related_Spectrum_Disorders|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 3,
    "Progressive_sclerosing_poliodystrophy|not_provided|not_specified|POLG-related_disorder": 1,
    "POLG-related_disorder|Mitochondrial_disease|not_specified|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 5,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_provided": 8,
    "not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases": 11,
    "Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|not_specified": 2,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 2,
    "POLG-Related_Spectrum_Disorders|Association_with_valproate-induced_liver_toxicity|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Mitochondrial_disease|Fanconi_anemia": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|Spinocerebellar_ataxia_with_epilepsy|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_provided|POLG-related_disorder": 1,
    "Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases": 16,
    "not_specified|not_provided|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|not_specified": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_4b|not_specified|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 14,
    "POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "not_specified|not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_disease": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 5,
    "not_specified|not_provided|Mitochondrial_disease|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|Abnormality_of_the_nervous_system|Childhood_myocerebrohepatopathy_spectrum|Mitochondrial_DNA_depletion_syndrome|Recessive_mitochondrial_ataxia_syndrome|Mitochondrial_disease|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_DNA_depletion_syndrome": 2,
    "POLG-Related_Spectrum_Disorders|not_provided|Progressive_sclerosing_poliodystrophy|POLG-related_disorder": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "not_provided|Inborn_genetic_diseases|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|not_specified|Inborn_genetic_diseases": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1": 4,
    "POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy": 5,
    "not_specified|not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|Spinocerebellar_ataxia_with_epilepsy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions": 1,
    "Hereditary_spastic_paraplegia|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy": 6,
    "Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_disease": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|POLG-Related_Spectrum_Disorders": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|POLG-Related_Spectrum_Disorders": 2,
    "Progressive_sclerosing_poliodystrophy|not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy|not_specified": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 3,
    "not_provided|POLG-Related_Spectrum_Disorders": 3,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|not_provided|POLG-Related_Spectrum_Disorders|not_specified": 1,
    "POLG-related_disorder|not_specified|Progressive_sclerosing_poliodystrophy": 2,
    "not_provided|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 8,
    "not_provided|POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "POLG-Related_Spectrum_Disorders|Autosomal_dominant_non-syndromic_intellectual_disability|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|not_provided|See_cases": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|POLG-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia_with_epilepsy|Mitochondrial_DNA_depletion_syndrome|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Early-onset_Parkinson_disease_20|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|EEG_abnormality": 1,
    "POLG-Related_Spectrum_Disorders|not_provided|Progressive_sclerosing_poliodystrophy": 4,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_provided": 5,
    "POLG-Related_Spectrum_Disorders|not_specified|not_provided|Fanconi_anemia|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "not_specified|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "not_provided|not_specified|Progressive_sclerosing_poliodystrophy": 6,
    "Progressive_sclerosing_poliodystrophy|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 2,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided|Inborn_genetic_diseases": 1,
    "Childhood_myocerebrohepatopathy_spectrum": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy": 4,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|not_provided|POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|POLG-Related_Spectrum_Disorders|not_provided": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|not_provided|POLG-related_disorder": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy|POLG-related_disorder": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 1,
    "not_provided|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Polyneuropathy": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b|Inborn_genetic_diseases|not_specified|POLG-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_provided|not_specified|POLG-Related_Spectrum_Disorders|Fanconi_anemia|Progressive_sclerosing_poliodystrophy": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|not_provided|POLG-Related_Spectrum_Disorders": 1,
    "Inborn_genetic_diseases|Spinocerebellar_atrophy|POLG-related_disorder|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_1|not_specified|Hereditary_spastic_paraplegia|not_provided|MELAS_syndrome": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Hereditary_spastic_paraplegia|POLG-related_disorder": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|POLG-related_disorder": 6,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_disease|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 4,
    "Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders": 1,
    "Progressive_sclerosing_poliodystrophy|not_specified|POLG-related_disorder": 3,
    "Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_disease": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "POLG-related_disorder|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Childhood_myocerebrohepatopathy_spectrum|Spinocerebellar_ataxia_with_epilepsy|not_provided|POLG-Related_Spectrum_Disorders|Tip-toe_gait": 1,
    "POLG-Related_Spectrum_Disorders|not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy|not_provided|Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 2,
    "Mitochondrial_DNA_depletion_syndrome|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|POLG-related_disorder|not_provided": 1,
    "Mitochondrial_disease|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_provided|not_specified": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_specified": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|POLG-related_disorder|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_provided|MELAS_syndrome": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_specified|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "Mitochondrial_DNA_depletion_syndrome|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|POLG-related_disorder|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-Related_Spectrum_Disorders|Mitochondrial_DNA_depletion_syndrome|Inborn_genetic_diseases|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|POLG-related_disorder|Hereditary_spastic_paraplegia|not_provided|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_digenic": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 2,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided": 1,
    "not_specified|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-Related_Spectrum_Disorders|POLG-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|not_specified|Progressive_sclerosing_poliodystrophy|not_provided": 2,
    "Progressive_sclerosing_poliodystrophy|not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "POLG-related_disorder|not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 2,
    "POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy|Tip-toe_gait": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_provided|not_specified": 1,
    "POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|POLG-related_disorder|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 2,
    "POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Neonatal_seizure": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome": 1,
    "not_provided|POLG-related_disorder": 3,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders": 2,
    "POLG-Related_Spectrum_Disorders|not_provided": 2,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders": 3,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Mitochondrial_disease|Progressive_sclerosing_poliodystrophy": 2,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|POLG-related_disorder|POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_specified|not_provided|Mitochondrial_disease|Spinocerebellar_ataxia_with_epilepsy": 1,
    "not_provided|POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy": 2,
    "not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|not_specified": 2,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|not_specified": 1,
    "Vascular_dementia|POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "Spinocerebellar_ataxia_with_epilepsy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|POLG-Related_Spectrum_Disorders|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|POLG-related_disorder|Hereditary_spastic_paraplegia|not_provided|Mitochondrial_disease|Tip-toe_gait": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided|Intellectual_disability|Tip-toe_gait": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|POLG-related_disorder": 6,
    "Progressive_sclerosing_poliodystrophy|not_provided|Hereditary_spastic_paraplegia": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_specified": 4,
    "Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|POLG-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|not_specified|POLG-related_disorder": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-Related_Spectrum_Disorders|not_specified|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|not_specified": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|not_provided": 2,
    "POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Limb-girdle_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_specified": 4,
    "not_provided|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Progressive_sclerosing_poliodystrophy|See_cases|POLG-Related_Spectrum_Disorders|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_specified": 1,
    "not_specified|POLG-Related_Spectrum_Disorders|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_specified|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy": 1,
    "not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Hereditary_spastic_paraplegia|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Progressive_sclerosing_poliodystrophy|POLG-related_disorder": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_1|Inborn_genetic_diseases|POLG-related_disorder|not_provided|not_specified|Hereditary_spastic_paraplegia|Global_developmental_delay|Mitochondrial_disease|Tip-toe_gait|Abnormality_of_the_nervous_system|See_cases|Hypertrophic_cardiomyopathy": 1,
    "Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_specified|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|not_provided|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "Premature_ovarian_failure|not_specified|POLG-related_disorder|Inborn_genetic_diseases": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|not_provided": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|Inborn_genetic_diseases|not_provided": 1,
    "POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_specified": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|Idiopathic_camptocormia|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Mitochondrial_disease|Progressive_sclerosing_poliodystrophy|Tip-toe_gait": 1,
    "Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|POLG-related_disorder|not_provided": 1,
    "POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|not_specified|not_provided|Spinocerebellar_ataxia_with_epilepsy": 1,
    "POLG-related_disorder|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|not_provided": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|not_specified|not_provided": 1,
    "Lennox-Gastaut_syndrome|POLG-Related_Spectrum_Disorders|POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Mitochondrial_disease": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|POLG-related_disorder|Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|not_provided|Hereditary_spastic_paraplegia|Mitochondrial_disease|Spinocerebellar_ataxia_with_epilepsy|Tip-toe_gait|Intellectual_disability|Neurodevelopmental_delay": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_specified|POLG-related_disorder|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "not_provided|POLG-Related_Spectrum_Disorders|POLG-related_disorder|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_specified|POLG-Related_Spectrum_Disorders": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome|not_provided|POLG-related_disorder": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|not_specified|Hereditary_spastic_paraplegia|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Global_developmental_delay|Generalized_epilepsy|Obesity": 1,
    "Neurodevelopmental_delay|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|POLG-related_disorder|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "POLG-related_disorder|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Progressive_sclerosing_poliodystrophy": 3,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_specified|POLG-Related_Spectrum_Disorders|Charcot-Marie-Tooth_disease": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 2,
    "not_provided|Progressive_sclerosing_poliodystrophy|Tip-toe_gait": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1": 1,
    "Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_provided": 1,
    "not_specified|not_provided|MELAS_syndrome|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|not_provided|Hereditary_spastic_paraplegia|Mitochondrial_DNA_depletion_syndrome|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1|not_specified": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Mitochondrial_DNA_depletion_syndrome|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided|Hereditary_spastic_paraplegia|Tip-toe_gait": 1,
    "Mitochondrial_DNA_depletion_syndrome|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|Charcot-Marie-Tooth_disease_axonal_type_2U|POLG-related_disorder|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_specified|not_provided|Hereditary_spastic_paraplegia|Tip-toe_gait": 1,
    "Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_1|POLG-Related_Spectrum_Disorders|Mitochondrial_DNA_depletion_syndrome|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Global_developmental_delay|Mitochondrial_disease|Tip-toe_gait|Abnormality_of_the_nervous_system|See_cases|Hypertrophic_cardiomyopathy": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|POLG-related_disorder|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome": 1,
    "Abnormality_of_corpus_callosum|Mitochondrial_DNA_depletion_syndrome|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Seizure|Autism|POLG-Related_Spectrum_Disorders|POLG-related_disorder|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome|Primary_progressive_multiple_sclerosis|not_provided": 1,
    "Mitochondrial_disease|POLG-related_disorder|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|not_provided|POLG-Related_Spectrum_Disorders": 1,
    "Inborn_genetic_diseases|not_specified|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy": 50,
    "Progressive_sclerosing_poliodystrophy|POLG-related_disorder|not_provided|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_1|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|Failure_to_thrive|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|Hereditary_spastic_paraplegia": 1,
    "not_specified|not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "POLG-Related_Spectrum_Disorders|not_provided|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "POLG-related_disorder|Progressive_sclerosing_poliodystrophy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|POLG-related_disorder|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Mitochondrial_DNA_depletion_syndrome|Primary_progressive_multiple_sclerosis|POLG-Related_Spectrum_Disorders|POLG-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Mitochondrial_disease|Progressive_sclerosing_poliodystrophy|Intellectual_disability": 1,
    "Progressive_sclerosing_poliodystrophy|not_specified|POLG-related_disorder|not_provided": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|not_provided|not_specified|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "See_cases|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "Hereditary_skeletal_muscle_disorder|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "not_specified|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Mitochondrial_disease|not_specified": 1,
    "Recessive_mitochondrial_ataxia_syndrome|POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Mitochondrial_DNA_depletion_syndrome_4b|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Autosomal_recessive_progressive_external_ophthalmoplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia|not_specified": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|Neuromuscular_disease|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_DNA_depletion_syndrome_4b|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|POLG-related_disorder|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|not_specified|not_provided|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "Inborn_genetic_diseases|not_specified|POLG-related_disorder|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Inborn_genetic_diseases|POLG-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|POLG-related_disorder|not_provided": 1,
    "Progressive_sclerosing_poliodystrophy|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b": 1,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|not_provided|Hereditary_spastic_paraplegia|POLG-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_sclerosing_poliodystrophy|not_provided": 1,
    "Inborn_genetic_diseases|POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_sclerosing_poliodystrophy": 1,
    "POLG-related_disorder|not_provided|Progressive_sclerosing_poliodystrophy|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Mitochondrial_DNA_depletion_syndrome_4b|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1": 1,
    "not_provided|Progressive_sclerosing_poliodystrophy|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "POLG-Related_Spectrum_Disorders|Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|POLG-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_1|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_1|Progressive_sclerosing_poliodystrophy|Mitochondrial_DNA_depletion_syndrome_4b|Mitochondrial_DNA_depletion_syndrome_1|Sensory_ataxic_neuropathy|_dysarthria|_and_ophthalmoparesis": 1,
    "Intellectual_disability|not_provided|Progressive_sclerosing_poliodystrophy": 1,
    "Mitochondrial_DNA_depletion_syndrome_4b|Progressive_sclerosing_poliodystrophy": 1,
    "Progressive_sclerosing_poliodystrophy|POLG-Related_Spectrum_Disorders|POLG-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Acrocallosal_syndrome|not_provided": 29,
    "not_provided|Acrocallosal_syndrome": 49,
    "Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 151,
    "Acrocallosal_syndrome|Inborn_genetic_diseases": 20,
    "KIF7-related_disorder": 13,
    "not_provided|Acrocallosal_syndrome|not_specified": 2,
    "KIF7-related_disorder|Intellectual_disability|Acrocallosal_syndrome|not_provided": 1,
    "Acrocallosal_syndrome|Joubert_syndrome|not_provided|Intellectual_disability": 1,
    "Acrocallosal_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Acrocallosal_syndrome": 9,
    "KIF7-related_disorder|Acrocallosal_syndrome|not_provided": 1,
    "not_specified|not_provided|Acrocallosal_syndrome": 12,
    "KIF7-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Acrocallosal_syndrome": 1,
    "Acrocallosal_syndrome|Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 4,
    "not_provided|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 5,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 17,
    "KIF7-related_disorder|Acrocallosal_syndrome": 6,
    "Acrocallosal_syndrome|not_specified|not_provided": 6,
    "not_provided|not_specified|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome": 1,
    "not_specified|KIF7-related_disorder|Acrocallosal_syndrome": 1,
    "Inborn_genetic_diseases|Acrocallosal_syndrome": 34,
    "Acrocallosal_syndrome|KIF7-related_disorder": 18,
    "not_provided|KIF7-related_disorder|Acrocallosal_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Hydrolethalus_syndrome_2|KIF7-related_disorder|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided": 7,
    "not_provided|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 6,
    "not_specified|Acrocallosal_syndrome|not_provided": 9,
    "Acrocallosal_syndrome|not_specified": 11,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 3,
    "Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Inborn_genetic_diseases": 18,
    "Intellectual_disability|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2": 1,
    "not_specified|Acrocallosal_syndrome": 8,
    "Acrocallosal_syndrome|Inborn_genetic_diseases|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 2,
    "not_provided|Inborn_genetic_diseases|Acrocallosal_syndrome": 4,
    "not_provided|Acrocallosal_syndrome|KIF7-related_disorder": 1,
    "not_specified|Hydrolethalus_syndrome_2|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome": 1,
    "KIF7-related_disorder|Inborn_genetic_diseases|not_provided|Acrocallosal_syndrome": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 4,
    "Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "Acrocallosal_syndrome|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Inborn_genetic_diseases": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Joubert_syndrome_12": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_specified|not_provided|Scoliosis|_isolated|_susceptibility_to|_1": 1,
    "not_specified|Acrocallosal_syndrome|KIF7-related_disorder": 1,
    "KIF7-related_disorder|not_provided|Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 1,
    "Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|not_provided": 8,
    "KIF7-related_disorder|not_provided|Acrocallosal_syndrome": 2,
    "Acrocallosal_syndrome|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 6,
    "Inborn_genetic_diseases|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 4,
    "Hydrolethalus_syndrome_2|Acrocallosal_syndrome|not_specified|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided": 1,
    "not_provided|not_specified|Acrocallosal_syndrome": 3,
    "Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|not_specified|not_provided": 1,
    "Intellectual_disability|Acrocallosal_syndrome": 2,
    "Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 2,
    "not_provided|Acrocallosal_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 1,
    "Acrocallosal_syndrome|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|not_specified|Inborn_genetic_diseases": 1,
    "Hydrolethalus_syndrome_2|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided|Inborn_genetic_diseases": 1,
    "Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|not_provided": 2,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|not_specified|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_specified": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome|not_provided": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Acrocallosal_syndrome|not_provided": 3,
    "not_provided|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 3,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome|not_provided": 2,
    "Hydrolethalus_syndrome_2|not_specified|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 1,
    "Acrocallosal_syndrome|KIF7-related_disorder|Inborn_genetic_diseases": 1,
    "Acrocallosal_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|KIF7-related_disorder": 2,
    "KIF7-related_disorder|Inborn_genetic_diseases|Acrocallosal_syndrome": 1,
    "Nephronophthisis|not_provided|not_specified|Acrocallosal_syndrome|Intellectual_disability": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome|Inborn_genetic_diseases": 2,
    "Acrocallosal_syndrome|not_provided|Inborn_genetic_diseases": 6,
    "not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome": 1,
    "Hydrolethalus_syndrome_2|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided": 2,
    "not_provided|Acrocallosal_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 1,
    "not_specified|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2": 1,
    "KIF7-related_disorder|Acrocallosal_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|KIF7-related_disorder|not_provided|Acrocallosal_syndrome": 1,
    "Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_specified|not_provided": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Inborn_genetic_diseases": 6,
    "Hydrolethalus_syndrome_2|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_specified|Acrocallosal_syndrome": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Intellectual_disability|Inborn_genetic_diseases|not_provided": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|Hydrolethalus_syndrome_2": 3,
    "Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 1,
    "Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "KIF7-related_disorder|not_specified": 1,
    "Acrocallosal_syndrome|KIF7-related_disorder|not_provided": 1,
    "Acrocallosal_syndrome|not_provided|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 1,
    "not_specified|Inborn_genetic_diseases|Acrocallosal_syndrome|not_provided": 1,
    "Acrocallosal_syndrome|not_provided|not_specified": 1,
    "Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided|Acrocallosal_syndrome": 1,
    "Hydrolethalus_syndrome|Acrocallosal_syndrome|Inborn_genetic_diseases|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|not_provided": 1,
    "Acrocallosal_syndrome|not_provided|KIF7-related_disorder": 3,
    "KIF7-related_disorder|not_specified|not_provided|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 1,
    "KIF7-related_disorder|Acrocallosal_syndrome|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 1,
    "JOUBERT_SYNDROME_12/15|_DIGENIC|Joubert_syndrome_12": 1,
    "Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia|_Al-Gazali_type": 1,
    "not_specified|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2|Acrocallosal_syndrome|Inborn_genetic_diseases": 1,
    "Short-limb_skeletal_dysplasia_with_severe_combined_immunodeficiency": 1,
    "not_provided|Inborn_genetic_diseases|Acrocallosal_syndrome|KIF7-related_disorder": 1,
    "KIF7-related_disorder|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome|not_provided": 1,
    "KIF7-related_disorder|not_specified|not_provided|Acrocallosal_syndrome": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|KIF7-related_ciliopathy_spectrum_disorder|KIF7-related_disorder|not_provided": 1,
    "Acrocallosal_syndrome|Male_infertility_due_to_gonadal_dysgenesis_or_sperm_disorder|Cerebellar_ataxia|Postaxial_foot_polydactyly|Ventriculomegaly|Postaxial_hand_polydactyly|Strabismus|Nystagmus|Spasticity": 1,
    "Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Acrocallosal_syndrome": 1,
    "not_provided|Acrocallosal_syndrome|KIF7-related_disorder|Hydrolethalus_syndrome_2|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Inborn_genetic_diseases": 1,
    "Acrocallosal_syndrome|not_provided|Inborn_genetic_diseases|Multiple_epiphyseal_dysplasia|_Al-Gazali_type|Hydrolethalus_syndrome_2": 1,
    "not_provided|Joubert_syndrome_12": 1,
    "Acrocallosal_syndrome|Hydrolethalus_syndrome_2": 1,
    "KIF7-related_ciliopathy_spectrum_disorder|Acrocallosal_syndrome|not_provided": 1,
    "Acrocallosal_syndrome|Intellectual_disability": 1,
    "PLIN1-related_familial_partial_lipodystrophy": 14,
    "PLIN1-related_disorder": 9,
    "PLIN1-related_disorder|not_provided": 2,
    "PLIN1-related_familial_partial_lipodystrophy|not_provided": 2,
    "not_specified|PLIN1-related_familial_partial_lipodystrophy|not_provided": 2,
    "not_specified|Monogenic_diabetes|PLIN1-related_disorder": 1,
    "PLIN1-related_disorder|not_specified|not_provided|PLIN1-related_familial_partial_lipodystrophy|Monogenic_diabetes": 1,
    "not_provided|PLIN1-related_familial_partial_lipodystrophy": 1,
    "PLIN1-related_familial_partial_lipodystrophy|not_specified|not_provided": 1,
    "not_specified|PLIN1-related_disorder": 1,
    "PLIN1-related_disorder|not_specified": 1,
    "PLIN1-related_disorder|Monogenic_diabetes|not_provided": 1,
    "PLIN1-related_familial_partial_lipodystrophy|not_specified": 1,
    "Autistic_spectrum_disorder_with_isolated_skills": 1,
    "MESP1-related_disorder|not_provided": 8,
    "MESP1-related_disorder": 3,
    "not_provided|MESP1-related_disorder": 11,
    "not_specified|not_provided|MESP1-related_disorder": 1,
    "not_specified|Spondylocostal_dysostosis|not_provided": 1,
    "Spondylocostal_dysostosis_2|_autosomal_recessive": 83,
    "not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive": 21,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|not_provided": 19,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|not_provided|MESP2-related_disorder": 1,
    "not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive|MESP2-related_disorder": 2,
    "MESP2-related_disorder|Inborn_genetic_diseases|Spondylocostal_dysostosis_2|_autosomal_recessive|not_provided": 1,
    "not_provided|MESP2-related_disorder|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive": 2,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_specified|Spondylocostal_dysostosis_2|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|MESP2-related_disorder|not_provided|not_specified": 1,
    "MESP2-related_disorder|not_provided": 4,
    "not_specified|Spondylocostal_dysostosis_2|_autosomal_recessive": 2,
    "not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive|not_specified": 2,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|not_provided|not_specified": 1,
    "not_provided|MESP2-related_disorder": 1,
    "not_specified|Spondylocostal_dysostosis_2|_autosomal_recessive|not_provided": 2,
    "not_provided|not_specified|Spondylocostal_dysostosis_2|_autosomal_recessive": 3,
    "not_provided|Spondylocostal_dysostosis|not_specified|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "MESP2-related_disorder|Spondylocostal_dysostosis_2|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "not_provided|Inborn_genetic_diseases|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_2|_autosomal_recessive|MESP2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "not_provided|Spondylocostal_dysostosis": 2,
    "ANPEP-related_disorder": 1,
    "ANPEP-related_disorder|not_provided": 2,
    "D-2-hydroxyglutaric_aciduria_2": 142,
    "Inborn_genetic_diseases|D-2-hydroxyglutaric_aciduria_2": 3,
    "IDH2-related_disorder|Enchondromatosis|not_specified|not_provided|D-2-hydroxyglutaric_aciduria_2": 1,
    "not_provided|D-2-hydroxyglutaric_aciduria_2": 7,
    "D-2-hydroxyglutaric_aciduria_2|not_specified": 6,
    "not_specified|D-2-hydroxyglutaric_aciduria_2": 1,
    "D-2-hydroxyglutaric_aciduria_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|D-2-hydroxyglutaric_aciduria_2": 1,
    "D-2-hydroxyglutaric_aciduria_2|not_provided|not_specified": 1,
    "not_provided|not_specified|D-2-hydroxyglutaric_aciduria_2": 1,
    "not_specified|not_provided|D-2-hydroxyglutaric_aciduria_2": 4,
    "IDH2-related_disorder|D-2-hydroxyglutaric_aciduria_2": 2,
    "D-2-hydroxyglutaric_aciduria_2|IDH2-related_disorder|not_specified|not_provided": 1,
    "IDH2-related_disorder|not_specified|not_provided|D-2-hydroxyglutaric_aciduria_2": 1,
    "not_provided|D-2-hydroxyglutaric_aciduria_2|Enchondromatosis|not_specified": 1,
    "D-2-hydroxyglutaric_aciduria_2|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|D-2-hydroxyglutaric_aciduria_2": 2,
    "Acute_myocardial_infarction": 4,
    "IDH2-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|D-2-hydroxyglutaric_aciduria_2": 1,
    "Inborn_genetic_diseases|D-2-hydroxyglutaric_aciduria_2|not_provided": 1,
    "D-2-hydroxyglutaric_aciduria_2|not_provided|IDH2-related_disorder": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_3": 6,
    "not_specified|not_provided|CIB1-related_disorder": 1,
    "CIB1-related_disorder|not_provided": 3,
    "not_provided|CIB1-related_disorder": 3,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_3|not_provided": 1,
    "CIB1-related_disorder": 2,
    "not_provided|CIB1-related_disorder|not_specified": 1,
    "IQGAP1-related_disorder": 4,
    "IQGAP1-associated_immune_condition": 1,
    "Bloom_syndrome": 1902,
    "Bloom_syndrome|not_specified": 4,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 680,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 759,
    "BLM-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Bloom_syndrome": 1,
    "BLM-related_disorder": 2,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BLM-related_disorder": 1,
    "Bloom_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 32,
    "Bloom_syndrome|not_provided": 20,
    "not_specified|Bloom_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_provided": 37,
    "Bloom_syndrome|BLM-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 38,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|BLM-related_disorder": 2,
    "not_provided|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 39,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 10,
    "Bloom_syndrome|BLM-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Bloom_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Microcephaly|BLM-related_disorder|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|BLM-related_disorder|Bloom_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Bloom_syndrome": 13,
    "not_provided|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Bloom_syndrome": 54,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Bloom_syndrome": 16,
    "Bloom_syndrome|BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Bloom_syndrome": 19,
    "Bloom_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 8,
    "Bloom_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 23,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Bloom_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 2,
    "BLM-related_disorder|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "Bloom_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_specified|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Bloom_syndrome|not_provided": 1,
    "not_specified|Bloom_syndrome": 7,
    "BLM-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 1,
    "not_specified|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 8,
    "Bloom_syndrome|BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Microcephaly|not_provided|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Bloom_syndrome": 2,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 4,
    "Bloom_syndrome|BLM-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|BLM-related_disorder|not_specified": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Hereditary_cancer|not_provided|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BLM-related_disorder|Bloom_syndrome": 3,
    "Hereditary_cancer|not_specified|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|BLM-related_disorder|not_specified|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|Ovarian_cancer": 1,
    "Bloom_syndrome|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Bloom_syndrome": 4,
    "Hereditary_cancer|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BLM-related_disorder": 1,
    "not_provided|Bloom_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|not_specified|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Bloom_syndrome|not_provided": 1,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_provided": 2,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Bloom_syndrome": 1,
    "Bloom_syndrome|BLM-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|BLM-related_disorder|not_specified|not_provided": 1,
    "Ovarian_cancer|Bloom_syndrome": 2,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Bloom_syndrome": 4,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|BLM-related_disorder": 1,
    "not_provided|not_specified|Bloom_syndrome": 1,
    "not_specified|not_provided|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer|Bloom_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Bloom_syndrome|BLM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Bloom_syndrome": 1,
    "Bloom_syndrome|not_provided|BLM-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Bloom_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|BLM-related_disorder|not_provided": 1,
    "not_specified|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Bloom_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Bloom_syndrome|not_provided": 3,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Bloom_syndrome|not_specified": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Bloom_syndrome|BLM-related_disorder": 2,
    "not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 1,
    "Hereditary_disease|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Microcephaly|Bloom_syndrome": 1,
    "BLM-related_disorder|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|BLM-related_disorder|not_specified|Bloom_syndrome|not_provided": 1,
    "Bloom_syndrome|Colorectal_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Bloom_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_provided|BLM-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Ovarian_cancer|Bloom_syndrome": 1,
    "Bloom_syndrome|BLM-related_disorder": 1,
    "not_specified|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BLM-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|not_provided|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|BLM-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BLM-related_disorder|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Bloom_syndrome": 1,
    "Familial_cancer_of_breast|Endometrial_carcinoma|Colorectal_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BLM-related_disorder|Bloom_syndrome": 1,
    "Bloom_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "BLM-related_disorder|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Bloom_syndrome": 2,
    "not_provided|Bloom_syndrome|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Bloom_syndrome|BLM-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Bloom_syndrome": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|BLM-related_disorder|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BLM-related_disorder|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Bloom_syndrome|BLM-related_disorder|not_provided": 1,
    "BLM-related_disorder|not_provided|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|Olaparib_response": 1,
    "Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BLM-related_disorder|not_provided": 1,
    "BLM-related_disorder|Bloom_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Bloom_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Bloom_syndrome|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|Bloom_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Bloom_syndrome|not_specified": 1,
    "not_provided|BLM-related_disorder": 1,
    "Cholestasis-edema_syndrome|_Norwegian_type|Osteootohepatoenteric_syndrome|not_provided": 1,
    "not_provided|UNC45A-related_disorder": 13,
    "Osteootohepatoenteric_syndrome": 12,
    "Osteootohepatoenteric_syndrome|not_provided": 2,
    "not_provided|Osteootohepatoenteric_syndrome": 3,
    "UNC45A-related_disorder|not_provided": 9,
    "Increased_susceptibility_to_fractures|Diarrhea|UNC45A-associated_Cholestasis|Hearing_impairment|Osteootohepatoenteric_syndrome": 1,
    "Cholestasis-edema_syndrome|_Norwegian_type|not_provided": 1,
    "Inborn_genetic_diseases|UNC45A-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|UNC45A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|UNC45A-related_disorder": 1,
    "Diarrhea|Increased_susceptibility_to_fractures|Hearing_impairment|UNC45A-associated_Cholestasis": 1,
    "not_provided|Inborn_genetic_diseases|Osteootohepatoenteric_syndrome": 1,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 13,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12": 4,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|VPS33B-related_disorder": 3,
    "Cholestasis|_progressive_familial_intrahepatic|_12|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 55,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|not_provided|not_specified": 1,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_specified": 5,
    "Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 2,
    "VPS33B-related_disorder|not_provided": 7,
    "Cholestasis|_progressive_familial_intrahepatic|_12": 2,
    "VPS33B-related_disorder|not_provided|not_specified": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided": 3,
    "Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|VPS33B-related_disorder": 2,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Inborn_genetic_diseases": 1,
    "VPS33B-related_disorder": 10,
    "not_provided|VPS33B-related_disorder": 5,
    "not_specified|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided": 2,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12": 2,
    "Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 1,
    "Inborn_genetic_diseases|not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|VPS33B-related_disorder": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|not_provided": 3,
    "Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|VPS33B-related_disorder|not_provided": 2,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|VPS33B-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_provided|VPS33B-related_disorder": 2,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|VPS33B-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "VPS33B-related_disorder|Abnormal_bleeding|Thrombocytopenia|Cholestasis|_progressive_familial_intrahepatic|_12|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided": 1,
    "Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|not_provided": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Cholestasis|_progressive_familial_intrahepatic|_12": 1,
    "Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided": 5,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Cholestasis|_progressive_familial_intrahepatic|_12|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|VPS33B-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|VPS33B-related_disorder": 1,
    "VPS33B-related_disorder|not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 3,
    "not_specified|not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|VPS33B-related_disorder": 1,
    "VPS33B-related_disorder|Microcephaly|not_specified|not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 1,
    "VPS33B-related_disorder|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided": 1,
    "not_specified|not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Inborn_genetic_diseases": 3,
    "not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Inborn_genetic_diseases": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 1,
    "not_specified|VPS33B-related_disorder|not_provided": 1,
    "not_specified|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided|VPS33B-related_disorder|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|Inborn_genetic_diseases": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_provided|not_specified": 3,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|VPS33B-related_disorder": 2,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "Abnormal_bleeding|Thrombocytopenia|not_provided": 2,
    "Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 2,
    "Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|not_provided|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Cholestasis|_progressive_familial_intrahepatic|_12": 1,
    "not_provided|VPS33B-related_disorder|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1": 1,
    "not_provided|Arthrogryposis_with_renal_dysfunction_and_cholestasis_syndrome|not_specified": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_12|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|not_provided": 1,
    "VPS33B-related_disorder|not_specified|not_provided": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|not_specified": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive|Cholestasis|_progressive_familial_intrahepatic|_12|not_provided|Inborn_genetic_diseases": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_12|Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|Keratoderma-ichthyosis-deafness_syndrome|_autosomal_recessive": 1,
    "Arthrogryposis|_renal_dysfunction|_and_cholestasis_1|not_specified|not_provided": 1,
    "SV2B-related_disorder": 1,
    "ST8SIA2-related_disorder": 2,
    "not_specified|ST8SIA2-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94": 26,
    "Developmental_and_epileptic_encephalopathy_94|not_specified": 35,
    "Developmental_and_epileptic_encephalopathy_94|not_provided": 96,
    "not_specified|Developmental_and_epileptic_encephalopathy_94": 19,
    "not_provided|Developmental_and_epileptic_encephalopathy_94": 94,
    "not_specified|Developmental_and_epileptic_encephalopathy_94|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases": 22,
    "CHD2-related_disorder": 12,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy_94": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_provided|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_specified": 2,
    "CHD2-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy_94": 1,
    "not_provided|Seizure|Developmental_and_epileptic_encephalopathy_94": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_specified|not_provided": 5,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_provided": 10,
    "not_specified|Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases": 1,
    "not_specified|CHD2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases|not_provided": 12,
    "Developmental_and_epileptic_encephalopathy_94|CHD2-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy_94|not_specified|CHD2-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases|not_specified": 2,
    "CHD2-related_disorder|Developmental_and_epileptic_encephalopathy_94|not_provided": 2,
    "CHD2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases": 1,
    "CHD2-related_disorder|Developmental_and_epileptic_encephalopathy_94": 10,
    "Developmental_and_epileptic_encephalopathy_94|not_specified|Inborn_genetic_diseases": 2,
    "CHD2-related_disorder|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy_94|not_provided": 1,
    "Inborn_genetic_diseases|CHD2-related_disorder|Developmental_and_epileptic_encephalopathy_94": 1,
    "CHD2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy_94": 2,
    "not_provided|CHD2-related_disorder|Developmental_and_epileptic_encephalopathy_94": 2,
    "CHD2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_specified|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|Neurodevelopmental_disorder|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_specified|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy_94|CHD2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|Developmental_and_epileptic_encephalopathy_94": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_94|not_specified": 4,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy_94": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy_94|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94": 1,
    "not_provided|Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy_94": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|not_specified": 8,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy_94|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy_94|Intellectual_disability": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|CHD2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|CHD2-related_disorder|Inborn_genetic_diseases": 1,
    "Complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy_94|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "CHD2-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94": 1,
    "Developmental_and_epileptic_encephalopathy_94|Autism_spectrum_disorder": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy_94|CHD2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases": 5,
    "not_provided|Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_1|not_provided|Developmental_and_epileptic_encephalopathy_94": 1,
    "not_provided|History_of_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy_94": 1,
    "Complex_neurodevelopmental_disorder|not_provided|Developmental_and_epileptic_encephalopathy_94": 1,
    "Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases|CHD2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|Inborn_genetic_diseases": 4,
    "Developmental_and_epileptic_encephalopathy_94|Complex_neurodevelopmental_disorder|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Inborn_genetic_diseases|CHD2-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided|Developmental_and_epileptic_encephalopathy_94": 1,
    "CHD2-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy_94|not_provided": 1,
    "Seizure|Autistic_behavior|Developmental_and_epileptic_encephalopathy_94|not_provided|Complex_neurodevelopmental_disorder|CHD2-related_disorder": 1,
    "not_specified|Intellectual_disability|Developmental_and_epileptic_encephalopathy_94|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy_94|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_94|CHD2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|CHD2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_specified": 2,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_specified|not_provided|Developmental_and_epileptic_encephalopathy_94": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy_94|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|Intellectual_disability": 1,
    "CHD2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|CHD2-related_disorder|not_provided": 1,
    "CHD2-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy_94": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy_94": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_94|not_provided|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy_94|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy_94|not_provided|Epilepsy": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy_94": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy_94": 1,
    "MCTP2-related_disorder": 15,
    "MCTP2-related_disorder|not_provided": 8,
    "not_provided|MCTP2-related_disorder": 11,
    "not_provided|MCTP2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MCTP2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|MCTP2-related_disorder": 1,
    "NR2F2-related_disorder": 5,
    "NR2F2_associated_disorders": 7,
    "Congenital_heart_defects|_multiple_types|_4|46|xx_sex_reversal_5": 2,
    "Congenital_heart_defects|_multiple_types|_4|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|46|xx_sex_reversal_5": 1,
    "NR2F2-related_congenital_heart_defects": 1,
    "NR2F2-Releated_Disorders": 1,
    "Neurodevelopmental_disorder|Congenital_heart_defects|_multiple_types|_4": 1,
    "Congenital_heart_defects|_multiple_types|_4|Inborn_genetic_diseases": 1,
    "Congenital_heart_defects|_multiple_types|_4|NR2F2-related_disorder": 2,
    "Congenital_heart_defects|_multiple_types|_4|not_provided": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_4": 1,
    "Congenital_heart_defects|_multiple_types|_4|not_provided|Asplenia": 1,
    "46|xx_sex_reversal_5": 1,
    "ARRDC4-related_condition": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 384,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided": 60,
    "IGF1R-related_disorder|not_specified": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|Inborn_genetic_diseases": 1,
    "not_provided|IGF1R-related_disorder|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 2,
    "not_provided|IGF1R-related_disorder": 7,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 25,
    "IGF1R-related_disorder|not_provided": 12,
    "not_specified|not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 5,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|IGF1R-related_disorder|not_provided": 3,
    "IGF1R-related_disorder": 15,
    "IGF1R-related_disorder|not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 3,
    "IGF1R-related_disorder|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided": 3,
    "IGF1R-related_disorder|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided|not_specified": 1,
    "not_provided|Intellectual_disability|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "IGF1R-related_disorder|not_provided|not_specified|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "IGF1R-related_disorder|not_specified|not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 3,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided|not_specified": 2,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|IGF1R-related_disorder": 3,
    "not_provided|not_specified|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided|Inborn_genetic_diseases": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|Microcephaly": 1,
    "not_specified|IGF1R-related_disorder|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided": 1,
    "not_specified|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "not_specified|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided": 2,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|Inborn_genetic_diseases": 2,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided|Intellectual_disability": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_specified|not_provided": 5,
    "IGF1R-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "Inborn_genetic_diseases|not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "Growth_delay_due_to_insulin-like_growth_factor_I_resistance|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Growth_delay_due_to_insulin-like_growth_factor_I_resistance": 1,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_specified": 1,
    "IGF1R-related_disorder|not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|not_specified": 1,
    "not_provided|Growth_delay_due_to_insulin-like_growth_factor_I_resistance|Inborn_genetic_diseases|IGF1R-related_disorder": 1,
    "SYNM-related_disorder": 38,
    "SYNM-related_disorder|not_provided": 2,
    "not_specified|SYNM-related_disorder": 4,
    "SYNM-related_disorder|not_specified": 6,
    "Coronary_artery_disease|_autosomal_dominant|_1": 4,
    "MEF2A-related_disorder": 8,
    "not_provided|not_specified|Coronary_artery_disease/myocardial_infarction": 1,
    "Coronary_artery_disease/myocardial_infarction": 2,
    "MEF2A-related_disorder|not_specified": 1,
    "not_provided|Coronary_artery_disease|_autosomal_dominant|_1": 1,
    "not_specified|MEF2A-related_disorder": 1,
    "Weill-Marchesani_4_syndrome|_recessive": 188,
    "not_provided|Weill-Marchesani_4_syndrome|_recessive": 122,
    "Weill-Marchesani_4_syndrome|_recessive|not_provided": 23,
    "not_provided|not_specified|Weill-Marchesani_4_syndrome|_recessive": 4,
    "ADAMTS17-related_disorder|not_provided|Weill-Marchesani_4_syndrome|_recessive": 4,
    "not_provided|ADAMTS17-related_disorder": 8,
    "Weill-Marchesani_4_syndrome|_recessive|Inborn_genetic_diseases|not_provided": 5,
    "not_provided|Weill-Marchesani_4_syndrome|_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Weill-Marchesani_4_syndrome|_recessive": 2,
    "Weill-Marchesani_4_syndrome|_recessive|not_provided|Inborn_genetic_diseases": 2,
    "ADAMTS17-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Weill-Marchesani_4_syndrome|_recessive|not_provided": 5,
    "Weill-Marchesani_4_syndrome|_recessive|ADAMTS17-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Weill-Marchesani_4_syndrome|_recessive": 7,
    "Inborn_genetic_diseases|Weill-Marchesani_4_syndrome|_recessive": 3,
    "not_provided|Weill-Marchesani_4_syndrome|_recessive|ADAMTS17-related_disorder": 1,
    "not_specified|not_provided|Weill-Marchesani_4_syndrome|_recessive": 5,
    "Weill-Marchesani_4_syndrome|_recessive|not_specified|not_provided": 1,
    "ADAMTS17-related_disorder": 2,
    "not_specified|Weill-Marchesani_4_syndrome|_recessive|not_provided": 1,
    "ADAMTS17-related_disorder|Weill-Marchesani_4_syndrome|_recessive|not_provided": 1,
    "not_provided|Anterior_segment_dysgenesis": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_9": 4,
    "Autosomal_recessive_congenital_ichthyosis_9": 11,
    "CERS3-related_disorder|not_provided": 1,
    "CERS3-related_disorder": 3,
    "Autosomal_recessive_congenital_ichthyosis_9|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_9|Ichthyosis": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_9|not_provided": 1,
    "Abnormality_of_the_skin|Autosomal_recessive_congenital_ichthyosis_9": 1,
    "Inborn_genetic_diseases|not_provided|CERS3-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_27|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_recessive_27": 32,
    "LINS1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_27": 1,
    "LINS1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_27": 1,
    "Inborn_genetic_diseases|not_provided|LINS1-related_disorder": 2,
    "Intellectual_disability|Intellectual_disability|_autosomal_recessive_27": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_27": 2,
    "Inborn_genetic_diseases|LINS1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_27": 1,
    "Intellectual_disability|_autosomal_recessive_27|not_provided": 2,
    "not_specified|Intellectual_disability|_autosomal_recessive_27": 1,
    "Isolated_microphthalmia_8": 45,
    "ALDH1A3-related_disorder|not_provided|Isolated_microphthalmia_8": 1,
    "ALDH1A3-related_disorder": 5,
    "Isolated_microphthalmia_8|not_provided": 4,
    "ALDH1A3-related_disorder|Isolated_microphthalmia_8": 3,
    "ALDH1A3-related_disorder|not_provided": 1,
    "Isolated_anophthalmia-microphthalmia_syndrome": 4,
    "not_provided|Isolated_microphthalmia_8": 2,
    "Isolated_microphthalmia_8|ALDH1A3-related_disorder": 1,
    "Microphthalmia|Isolated_microphthalmia_8": 1,
    "Inborn_genetic_diseases|Isolated_microphthalmia_8": 1,
    "Isolated_microphthalmia_8|not_provided|ALDH1A3-related_disorder": 1,
    "Isolated_microphthalmia_8|not_provided|not_specified": 1,
    "not_provided|Isolated_microphthalmia_8|not_specified": 1,
    "Isolated_microphthalmia_8|Inborn_genetic_diseases": 1,
    "LRRK1-related_disorder|not_provided": 36,
    "Osteosclerotic_metaphyseal_dysplasia": 10,
    "not_provided|LRRK1-related_disorder": 39,
    "not_provided|Inborn_genetic_diseases|LRRK1-related_disorder": 3,
    "LRRK1-related_disorder": 7,
    "Inborn_genetic_diseases|LRRK1-related_disorder|not_provided": 1,
    "LRRK1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Osteosclerotic_metaphyseal_dysplasia": 1,
    "Osteosclerotic_metaphyseal_dysplasia|LRRK1-related_disorder|not_provided": 1,
    "Temtamy_preaxial_brachydactyly_syndrome": 108,
    "Temtamy_preaxial_brachydactyly_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "Temtamy_preaxial_brachydactyly_syndrome|not_provided": 7,
    "Inborn_genetic_diseases|Temtamy_preaxial_brachydactyly_syndrome": 12,
    "not_provided|Temtamy_preaxial_brachydactyly_syndrome": 19,
    "not_specified|not_provided|Temtamy_preaxial_brachydactyly_syndrome": 3,
    "Temtamy_preaxial_brachydactyly_syndrome|Inborn_genetic_diseases": 8,
    "Temtamy_preaxial_brachydactyly_syndrome|CHSY1-related_disorder": 2,
    "not_provided|Temtamy_preaxial_brachydactyly_syndrome|Inborn_genetic_diseases": 1,
    "Temtamy_preaxial_brachydactyly_syndrome|CHSY1-related_disorder|Inborn_genetic_diseases": 1,
    "CHSY1-related_disorder": 3,
    "CHSY1-related_disorder|not_specified|not_provided|Temtamy_preaxial_brachydactyly_syndrome": 1,
    "not_provided|Temtamy_preaxial_brachydactyly_syndrome|not_specified": 1,
    "CHSY1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Temtamy_preaxial_brachydactyly_syndrome": 2,
    "not_provided|not_specified|CHSY1-related_disorder|Temtamy_preaxial_brachydactyly_syndrome": 1,
    "Temtamy_preaxial_brachydactyly_syndrome|not_specified": 1,
    "TM2D3-related_disorder": 1,
    "TM2D3-related_disorder|NEUROCARDIORENAL_MALFORMATION_SYNDROME": 3,
    "Leukodystrophy|_hypomyelinating|_21": 4,
    "MPG-related_condition": 1,
    "not_provided|NPRL3-related_disorder": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_provided": 61,
    "Epilepsy|_familial_focal|_with_variable_foci_3": 617,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_3": 43,
    "NPRL3-related_disorder": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_specified": 2,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_3|not_specified": 2,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_provided|NPRL3-related_disorder": 2,
    "NPRL3-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_3": 4,
    "not_specified|Epilepsy|_familial_focal|_with_variable_foci_3|not_provided": 3,
    "not_provided|NPRL3-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_3": 5,
    "not_specified|Epilepsy|_familial_focal|_with_variable_foci_3": 4,
    "Epilepsy|_familial_focal|_with_variable_foci_3|Focal_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_3": 10,
    "NPRL3-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_3|not_provided": 3,
    "NPRL3-related_disorder|not_provided|Epilepsy|_familial_focal|_with_variable_foci_3": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|Inborn_genetic_diseases|not_provided": 6,
    "Epilepsy|_familial_focal|_with_variable_foci_3|Inborn_genetic_diseases": 19,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|NPRL3-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_3": 1,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_familial_focal|_with_variable_foci_3": 3,
    "not_provided|not_specified|Epilepsy|_familial_focal|_with_variable_foci_3": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_specified|not_provided": 2,
    "Epilepsy|_familial_focal|_with_variable_foci_3|NPRL3-related_disorder|not_provided": 1,
    "Seizure|not_provided|Epilepsy|_familial_focal|_with_variable_foci_3": 1,
    "Epilepsy|Epilepsy|_familial_focal|_with_variable_foci_3": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Seizure|Epilepsy|_familial_focal|_with_variable_foci_3": 1,
    "not_specified|NPRL3-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_3|not_provided": 1,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Familial_temporal_lobe_epilepsy_2": 1,
    "not_specified|Epilepsy|_familial_focal|_with_variable_foci_3|Inborn_genetic_diseases": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_3|not_provided": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|Intellectual_disability|not_provided": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 4,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_provided|Seizure": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_3|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "NPRL3-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_3|Inborn_genetic_diseases": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_3|Inborn_genetic_diseases": 1,
    "HEMOGLOBIN_LAMEN_ISLAND": 1,
    "alpha_Thalassemia": 103,
    "not_provided|HBA2-related_disorder|Heinz_body_anemia|Hemoglobin_H_disease|alpha_Thalassemia|Erythrocytosis|_familial|_7": 1,
    "alpha_Thalassemia|not_provided": 11,
    "Alpha-thalassemia_and_related_diseases|alpha_Thalassemia": 1,
    "not_specified|alpha_Thalassemia|not_provided": 2,
    "HBA2-related_disorder": 8,
    "alpha_Thalassemia|not_provided|Alpha-thalassemia|_Hmong_type": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided|Hemoglobin_H_disease|_nondeletional": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|Hemoglobin_H_disease|_nondeletional|not_provided": 1,
    "not_provided|alpha_Thalassemia": 10,
    "HEMOGLOBIN_ANTANANARIVO": 1,
    "not_provided|HEMOGLOBIN_BOYLE_HEIGHTS": 1,
    "not_provided|HEMOGLOBIN_KUROSAKI": 1,
    "not_specified|alpha_Thalassemia": 1,
    "HEMOGLOBIN_PARK_RIDGE|not_provided|alpha_Thalassemia": 1,
    "Heinz_body_anemia|alpha_Thalassemia|Hemoglobin_H_disease|Erythrocytosis|_familial|_7|not_specified": 1,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia": 4,
    "HEMOGLOBIN_J_(OXFORD)|HEMOGLOBIN_I_(INTERLAKEN)|HEMOGLOBIN_N_(COSENZA)": 1,
    "not_provided|HEMOGLOBIN_I|HEMOGLOBIN_I_(BURLINGTON)|HEMOGLOBIN_I_(PHILADELPHIA)|HEMOGLOBIN_I_(SKAMANIA)|HEMOGLOBIN_I_(TEXAS)": 1,
    "alpha_Thalassemia|not_provided|Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia": 1,
    "HEMOGLOBIN_NIKAIA": 1,
    "HEMOGLOBIN_LE_LAMENTIN": 1,
    "not_provided|Erythrocytosis|_familial|_7|alpha_Thalassemia|Hemoglobin_H_disease|Heinz_body_anemia": 1,
    "not_provided|alpha_Thalassemia|Alpha-thalassemia|_Dutch_type": 1,
    "Erythrocytosis|_familial|_7|alpha_Thalassemia|Heinz_body_anemia|Hemoglobin_H_disease|not_provided": 1,
    "HEMOGLOBIN_CAMPINAS": 1,
    "HEMOGLOBIN_SPANISH_TOWN": 1,
    "alpha_Thalassemia|Hemoglobin_H_disease|_nondeletional|not_provided|HEMOGLOBIN_AGRINIO": 1,
    "not_provided|HEMOGLOBIN_H_HYDROPS_FETALIS_SYNDROME": 1,
    "HEMOGLOBIN_G_(SINGAPORE)|HEMOGLOBIN_G_(CHINESE)|HEMOGLOBIN_G_(HONOLULU)|HEMOGLOBIN_G_(HONG_KONG)": 1,
    "not_provided|alpha_Thalassemia|Hemoglobin_H_disease|Heinz_body_anemia|Erythrocytosis|_familial|_7": 1,
    "not_provided|not_specified|alpha_Thalassemia": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided|Alpha-thalassemia|_Dutch_type": 1,
    "Abnormal_hemoglobin": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia": 1,
    "alpha_Thalassemia|not_provided|not_specified": 2,
    "not_provided|HBA2-related_disorder": 3,
    "HEMOGLOBIN_CHARTRES": 1,
    "HEMOGLOBIN_H_HYDROPS_FETALIS_SYNDROME|not_provided": 1,
    "HEMOGLOBIN_MANAWATU": 1,
    "Alpha_trait_thalassemia": 1,
    "Erythrocytosis|_familial|_7|HEMOGLOBIN_KANAGAWA": 1,
    "Thalassemia|not_provided": 1,
    "HEMOGLOBIN_HIROSAKI": 1,
    "alpha_Thalassemia|HEMOGLOBIN_L_(FERRARA)|HEMOGLOBIN_HASHARON|HEMOGLOBIN_SINAI|HEMOGLOBIN_SEALY|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided": 1,
    "HEMOGLOBIN_KURDISTAN": 1,
    "alpha_Thalassemia|HEMOGLOBIN_BIRMINGHAM_(USA)|HEMOGLOBIN_MONTGOMERY|not_provided|not_specified": 1,
    "HEMOGLOBIN_SAVARIA|not_provided": 1,
    "not_provided|HEMOGLOBIN_J_(SARDEGNA)": 1,
    "HEMOGLOBIN_GERLAND": 1,
    "HEMOGLOBIN_BOGHE": 1,
    "alpha_Thalassemia|not_provided|Alpha-thalassemia|_Dutch_type|HEMOGLOBIN_ZURICH_ALBISRIEDEN": 1,
    "not_provided|Non-immune_hydrops_fetalis|HEMOGLOBIN_H_HYDROPS_FETALIS_SYNDROME|alpha_Thalassemia": 1,
    "HEMOGLOBIN_J_(BUDA)|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_EVANS": 1,
    "HEMOGLOBIN_PART-DIEU": 1,
    "Heinz_body_anemia": 6,
    "alpha_Thalassemia|not_provided|HEMOGLOBIN_DARTMOUTH": 1,
    "HEMOGLOBIN_G_(PHILADELPHIA)|HEMOGLOBIN_KNOXVILLE-1|HEMOGLOBIN_STANLEYVILLE-I|HEMOGLOBIN_G_(BRISTOL)|HEMOGLOBIN_D_(BALTIMORE)|HEMOGLOBIN_D_(ST._LOUIS)|HEMOGLOBIN_D_(WASHINGTON)|HEMOGLOBIN_G_(AZAKUOLI)|HEMOGLOBIN_G_(KNOXVILLE)": 1,
    "HEMOGLOBIN_DECINES-CHARPIEU": 1,
    "HEMOGLOBIN_NORTON": 1,
    "HEMOGLOBIN_GOUDA": 1,
    "HEMOGLOBIN_WATTS": 1,
    "HEMOGLOBIN_AL-HAMMADI_RIYADH": 1,
    "HEMOGLOBIN_TOULON": 1,
    "HEMOGLOBIN_DAVENPORT": 1,
    "HEMOGLOBIN_CONAKRY": 1,
    "HEMOGLOBIN_PASSY": 1,
    "not_provided|HEMOGLOBIN_INKSTER|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_COLUMBIA_MISSOURI|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_CLINICO-MADRID|not_specified": 1,
    "HBA2-related_disorder|not_provided": 1,
    "HEMOGLOBIN_RAMPA": 1,
    "HEMOGLOBIN_CLINICO-MADRID|alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|Hemoglobin_H_disease|_nondeletional": 1,
    "Heinz_body_anemia|Erythrocytosis|_familial|_7|alpha_Thalassemia|Hemoglobin_H_disease|not_provided": 1,
    "not_provided|HEMOGLOBIN_MANITOBA": 1,
    "not_specified|HEMOGLOBIN_LOMBARD": 1,
    "Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia|Erythrocytosis|_familial|_7": 1,
    "Hemoglobin_H_disease|_nondeletional|Hemoglobin_H_disease|HEMOGLOBIN_SALLANCHES|alpha_Thalassemia|not_provided|Erythrocytosis|_familial|_7|Heinz_body_anemia": 1,
    "alpha_Thalassemia|HEMOGLOBIN_SUAN-DOK": 1,
    "HEMOGLOBIN_ANAMOSA": 1,
    "HEMOGLOBIN_SAN_ANTONIO": 1,
    "Hemoglobin_H_disease|not_provided": 1,
    "alpha_Thalassemia|not_specified": 2,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia|not_provided|HEMOGLOBIN_WESTMEAD": 1,
    "alpha_Thalassemia|HBA2-related_disorder|not_provided": 1,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|alpha_Thalassemia|Heinz_body_anemia|not_provided|Hemoglobin_Quong_Sze": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided|HEMOGLOBIN_PLASENCIA": 1,
    "Erythrocytosis|_familial|_7|alpha_Thalassemia|Hemoglobin_H_disease|Heinz_body_anemia|not_specified|not_provided|HEMOGLOBIN_TARRANT": 1,
    "not_specified|HEMOGLOBIN_SUN_PRAIRIE|alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided": 1,
    "Hemoglobin_H_disease|Erythrocytosis|_familial|_7|Heinz_body_anemia|alpha_Thalassemia": 1,
    "Hemoglobin_Val_de_Marne": 1,
    "Splenomegaly|Anemia|Heinz_body_anemia": 1,
    "not_specified|alpha_Thalassemia|not_provided|HBA2-related_disorder": 1,
    "alpha_Thalassemia|HEMOGLOBIN_WAYNE|not_provided": 1,
    "HEMOGLOBIN_HANAMAKI|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_FUKUI": 1,
    "HEMOGLOBIN_NATAL": 1,
    "Hemoglobin_H_disease|_nondeletional|not_provided|alpha_Thalassemia|HEMOGLOBIN_ICARIA|beta_Thalassemia": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|not_provided|Hemoglobin_H_disease|_nondeletional|Hemoglobin_constant_spring": 1,
    "not_provided|HEMOGLOBIN_SEAL_ROCK|alpha_Thalassemia": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|HEMOGLOBIN_KOYA_DORA|not_provided": 1,
    "not_provided|Hemoglobin_H_disease|_nondeletional|alpha_Thalassemia": 1,
    "alpha_Thalassemia|Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|not_provided": 1,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia|not_provided|Hemoglobin_H_disease|_nondeletional|beta_Thalassemia|Alpha-thalassemia-2|_nondeletional": 1,
    "Hemoglobin_H_disease|alpha_Thalassemia|beta_Thalassemia|Heinz_body_anemia|Erythrocytosis|_familial|_7|not_provided": 1,
    "alpha_Thalassemia|not_specified|Erythrocytosis|_familial|_7|not_provided": 1,
    "not_specified|not_provided|alpha_Thalassemia": 2,
    "alpha_Thalassemia|Methemoglobinemia|_alpha_type|Heinz_body_anemia|Hemoglobin_H_disease|Erythrocytosis|_familial|_7|not_provided": 1,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia|Methemoglobinemia|_alpha_type|not_provided": 2,
    "HEMOGLOBIN_THIONVILLE": 1,
    "HEMOGLOBIN_CHONGQING": 1,
    "HEMOGLOBIN_DOUALA": 1,
    "HEMOGLOBIN_KARACHI": 1,
    "alpha_Thalassemia|HEMOGLOBIN_J_(TORONTO)|not_provided": 1,
    "HEMOGLOBIN_DUNN": 1,
    "not_specified|HEMOGLOBIN_WOODVILLE": 1,
    "HEMOGLOBIN_SAWARA": 1,
    "Erythrocytosis|_familial|_7|alpha_Thalassemia|not_provided|HEMOGLOBIN_SWAN_RIVER": 1,
    "HEMOGLOBIN_FERNDOWN": 1,
    "not_provided|HEMOGLOBIN_TATRAS": 1,
    "HEMOGLOBIN_DELFZICHT": 1,
    "HEMOGLOBIN_WUMING|HEMOGLOBIN_J_(WENCHANG-WUMING)": 1,
    "HEMOGLOBIN_ANANTHARAJ": 1,
    "HEMOGLOBIN_ALBANY-GEORGIA|HEMOGLOBIN_ALBANY-SUMA": 1,
    "HEMOGLOBIN_J_(ALJEZUR)|HEMOGLOBIN_J_(PARIS_1)": 1,
    "not_provided|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|alpha_Thalassemia|Hemoglobin_H_disease|Heinz_body_anemia": 1,
    "HEMOGLOBIN_EVANSTON": 1,
    "alpha_Thalassemia|Methemoglobinemia|_alpha_type|Heinz_body_anemia|Erythrocytosis|_familial|_7|Hemoglobin_H_disease": 2,
    "Erythrocytosis|_familial|_7|not_specified|Methemoglobinemia|_alpha_type|Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia": 1,
    "HEMOGLOBIN_OTTAWA|HEMOGLOBIN_SIAM|not_provided": 1,
    "HEMOGLOBIN_I_(SKAMANIA)|HEMOGLOBIN_I_(TEXAS)|HEMOGLOBIN_I|HEMOGLOBIN_I_(BURLINGTON)|HEMOGLOBIN_I_(PHILADELPHIA)|not_provided|HBA1-related_disorder|not_specified": 1,
    "HEMOGLOBIN_HARBIN": 1,
    "HEMOGLOBIN_BEIJING": 1,
    "not_provided|HEMOGLOBIN_HANDSWORTH": 1,
    "HEMOGLOBIN_AL-AIN_ABU_DHABI": 1,
    "HEMOGLOBIN_J_(TASHIKUERGAN)": 1,
    "HEMOGLOBIN_NECKER_ENFANTS-MALADES": 1,
    "not_provided|alpha_Thalassemia|Methemoglobinemia|_alpha_type|Heinz_body_anemia|Hemoglobin_H_disease|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_HOBART": 1,
    "HEMOGLOBIN_FONTAINEBLEAU": 1,
    "HEMOGLOBIN_J_(NYANZA)": 1,
    "HEMOGLOBIN_J_(MEDELLIN)": 1,
    "HEMOGLOBIN_CHAD": 1,
    "HEMOGLOBIN_MEMPHIS": 1,
    "HEMOGLOBIN_REIMS": 1,
    "HEMOGLOBIN_G_(AUDHALI)": 1,
    "HEMOGLOBIN_LISBON": 1,
    "HEMOGLOBIN_LUXEMBOURG": 1,
    "not_specified|HEMOGLOBIN_RAMONA": 1,
    "HEMOGLOBIN_SHENYANG": 1,
    "HEMOGLOBIN_SHUANGFENG": 1,
    "HEMOGLOBIN_G_(FORT_WORTH)|HEMOGLOBIN_FORT_WORTH": 1,
    "HEMOGLOBIN_HEKINAN|not_provided": 1,
    "alpha_Thalassemia|Hemoglobin_H_disease|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Heinz_body_anemia|not_provided": 1,
    "HEMOGLOBIN_O_(PADOVA)|not_provided": 1,
    "Erythrocytosis|_familial|_7|alpha_Thalassemia|not_provided": 1,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Heinz_body_anemia|alpha_Thalassemia|Methemoglobinemia|_alpha_type": 2,
    "not_provided|Hemoglobin_H_disease|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Heinz_body_anemia|alpha_Thalassemia": 1,
    "HBA1-related_disorder|Hemoglobin_H_disease|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Heinz_body_anemia|alpha_Thalassemia|not_provided": 1,
    "not_provided|HEMOGLOBIN_OGI|HEMOGLOBIN_QUEENS": 1,
    "alpha_Thalassemia|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|HEMOGLOBIN_TAYBE|not_provided": 1,
    "HEMOGLOBIN_BOURMEDES": 1,
    "HEMOGLOBIN_CATONSVILLE": 1,
    "HEMOGLOBIN_KARIYA": 1,
    "HEMOGLOBIN_SARATOGA_SPRINGS": 1,
    "HEMOGLOBIN_MIYANO": 1,
    "HEMOGLOBIN_TORINO": 1,
    "HEMOGLOBIN_KAWACHI": 1,
    "Erythrocytosis|_familial|_7|not_provided|HEMOGLOBIN_MILLEDGEVILLE": 1,
    "HEMOGLOBIN_POITIERS": 1,
    "HEMOGLOBIN_OITA": 1,
    "HEMOGLOBIN_FORT_DE_FRANCE": 1,
    "HEMOGLOBIN_BARI": 1,
    "HEMOGLOBIN_ARYA|not_provided": 1,
    "HEMOGLOBIN_CORDELE": 1,
    "HEMOGLOBIN_TAGAWA_II|HEMOGLOBIN_UMI|HEMOGLOBIN_MUGINO|HEMOGLOBIN_YUKUHASHI-2|HEMOGLOBIN_KOKURA|HEMOGLOBIN_BEILINSON|HEMOGLOBIN_MICHIGAN-I|HEMOGLOBIN_MICHIGAN-II|HEMOGLOBIN_L_(GASLINI)": 1,
    "HEMOGLOBIN_J_(BISKRA)": 1,
    "HEMOGLOBIN_AICHI": 1,
    "HBA1-related_disorder|HEMOGLOBIN_RICCARTON|not_provided": 1,
    "HEMOGLOBIN_RUSS|not_provided": 1,
    "HEMOGLOBIN_J_(ABIDJAN)": 1,
    "HEMOGLOBIN_J_(ROVIGO)": 1,
    "not_provided|HEMOGLOBIN_J_(PARIS_2)|HEMOGLOBIN_UPPSALA|HEMOGLOBIN_MEXICO|HEMOGLOBIN_J|HEMOGLOBIN_J_(MEXICO)": 1,
    "HEMOGLOBIN_SHIMONOSEKI|HEMOGLOBIN_HIKOSHIMA": 1,
    "HEMOGLOBIN_ROUBAIX": 1,
    "HEMOGLOBIN_SHAARE_ZEDEK": 1,
    "HEMOGLOBIN_THAILAND": 1,
    "HEMOGLOBIN_PORT_HURON": 1,
    "HEMOGLOBIN_BELLIARD": 1,
    "HEMOGLOBIN_L_(PERSIAN_GULF)": 1,
    "HEMOGLOBIN_NORFOLK|HEMOGLOBIN_J_(NORFOLK)|HEMOGLOBIN_KAGOSHIMA|HEMOGLOBIN_NISHIK": 1,
    "HEMOGLOBIN_M_(GOTHENBURG)|HEMOGLOBIN_M_(OSAKA)|HEMOGLOBIN_M_(KISKUNHALAS)|HEMOGLOBIN_M_(BOSTON)|HEMOGLOBIN_GOTHENBURG": 1,
    "alpha_Thalassemia|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided|Hemoglobin_H_disease|_nondeletional|HEMOGLOBIN_ADANA": 1,
    "HEMOGLOBIN_TOTTORI": 1,
    "HEMOGLOBIN_DAGESTAN": 1,
    "HEMOGLOBIN_ZAMBIA": 1,
    "HEMOGLOBIN_J_(ANATOLIA)": 1,
    "alpha_Thalassemia|not_provided|Heinz_body_anemia|Hemoglobin_H_disease|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7": 1,
    "Hemoglobin_H_disease|_nondeletional|HEMOGLOBIN_AGHIA_SOPHIA|alpha_Thalassemia": 1,
    "HEMOGLOBIN_J_(PONTOISE)|HEMOGLOBIN_PONTOISE": 1,
    "Alpha-thalassemia|_Dutch_type": 1,
    "HEMOGLOBIN_G_(WAIMANALO)|HEMOGLOBIN_AIDA": 1,
    "not_provided|HEMOGLOBIN_Q_(INDIA)|alpha_Thalassemia": 1,
    "HEMOGLOBIN_PERSPOLIS": 1,
    "HEMOGLOBIN_GUANGZHOU|HEMOGLOBIN_HANGZHOU": 1,
    "HEMOGLOBIN_BOIS_GUILLAUME": 1,
    "alpha_Thalassemia|HBA1-related_disorder|not_provided": 1,
    "not_specified|HEMOGLOBIN_UBE-2|not_provided": 1,
    "HEMOGLOBIN_J_(HABANA)": 1,
    "HEMOGLOBIN_OZIERI": 1,
    "HEMOGLOBIN_FUCHU-I": 1,
    "HEMOGLOBIN_DANESHGAH-TEHRAN": 1,
    "not_provided|HEMOGLOBIN_G_(PEST)|not_specified": 1,
    "alpha_Thalassemia|not_provided|HEMOGLOBIN_KURASHIKI|HEMOGLOBIN_G_(TAICHUNG)|HEMOGLOBIN_Q|HEMOGLOBIN_Q_(THAILAND)|HEMOGLOBIN_MAHIDOL|HEMOGLOBIN_ASABARA": 1,
    "HEMOGLOBIN_LILLE": 1,
    "HEMOGLOBIN_CHAPEL_HILL": 1,
    "HEMOGLOBIN_MATSUE-OKI": 1,
    "HEMOGLOBIN_Q_(IRAN)": 1,
    "not_provided|HEMOGLOBIN_WINNIPEG": 1,
    "HEMOGLOBIN_DUAN": 1,
    "HEMOGLOBIN_MIZUSHI": 1,
    "HEMOGLOBIN_NOKO": 1,
    "HEMOGLOBIN_AZTEC": 1,
    "HEMOGLOBIN_GUIZHOU|HEMOGLOBIN_UTSUNOMIYA": 1,
    "HEMOGLOBIN_J_(SINGA)": 1,
    "HBA1-related_disorder|not_provided|alpha_Thalassemia|Heinz_body_anemia|Hemoglobin_H_disease|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_STANLEYVILLE-II": 1,
    "HEMOGLOBIN_MANTES-LA-JOLIE": 1,
    "HEMOGLOBIN_ANN_ARBOR": 1,
    "HEMOGLOBIN_NIGERIA": 1,
    "HEMOGLOBIN_GARDEN_STATE": 1,
    "not_provided|HBA1-related_disorder": 1,
    "HEMOGLOBIN_ETOBICOKE": 1,
    "not_provided|HEMOGLOBIN_G_(NORFOLK)": 1,
    "HEMOGLOBIN_ATAGO|alpha_Thalassemia": 1,
    "HEMOGLOBIN_MOABIT": 1,
    "HEMOGLOBIN_AUCKLAND": 1,
    "not_provided|HEMOGLOBIN_M_(IWATE)|HEMOGLOBIN_M_(KANKAKEE)|HEMOGLOBIN_M_(OLDENBURG)|HEMOGLOBIN_M_(SENDAI)|Methemoglobinemia|_alpha_type": 1,
    "HEMOGLOBIN_IWATA": 1,
    "Erythrocytosis|_familial|_7|HEMOGLOBIN_LOIRE": 1,
    "HEMOGLOBIN_VILLEURBANNE": 1,
    "HEMOGLOBIN_TOKYO": 1,
    "HEMOGLOBIN_TAMANO": 1,
    "HEMOGLOBIN_LUTON": 1,
    "not_provided|not_specified|HEMOGLOBIN_BUFFALO": 1,
    "not_provided|HEMOGLOBIN_J_(RAJAPPEN)": 1,
    "HEMOGLOBIN_HANDA|HEMOGLOBIN_MUNAKATA": 1,
    "not_provided|HEMOGLOBIN_BROUSSAIS|HEMOGLOBIN_J_(BROUSSAIS)|HEMOGLOBIN_TAGAWA_I": 1,
    "HEMOGLOBIN_PORT_PHILLIP": 1,
    "HEMOGLOBIN_CEMENELUM": 1,
    "HEMOGLOBIN_J_(CAPE_TOWN)|Erythrocytosis|_familial|_7": 1,
    "not_provided|Alpha-thalassemia|_Dutch_type": 1,
    "Erythrocytosis|_familial|_7|HEMOGLOBIN_CHESAPEAKE": 1,
    "HEMOGLOBIN_DIE": 1,
    "HEMOGLOBIN_TITUSVILLE": 1,
    "HEMOGLOBIN_SUNSHINE_SETH|not_provided": 1,
    "HEMOGLOBIN_SETIF": 1,
    "HEMOGLOBIN_CAPA": 1,
    "HEMOGLOBIN_ROANNE": 1,
    "HEMOGLOBIN_GODAVARI|not_specified": 1,
    "HEMOGLOBIN_DENMARK_HILL": 1,
    "not_provided|HEMOGLOBIN_ST._LUKE'S": 1,
    "not_specified|HEMOGLOBIN_G_(GEORGIA)": 1,
    "HEMOGLOBIN_FUCHU-II": 1,
    "HEMOGLOBIN_TURRIFF": 1,
    "HEMOGLOBIN_BEZIERS": 1,
    "Erythrocytosis|_familial|_7|Hemoglobin_H_disease|Methemoglobinemia|_alpha_type|Heinz_body_anemia|alpha_Thalassemia|not_provided": 1,
    "not_specified|HEMOGLOBIN_CHAROLLES": 1,
    "HEMOGLOBIN_CONTALDO": 1,
    "HEMOGLOBIN_OEGSTGEEST": 1,
    "HBA1-related_disorder": 3,
    "Heinz_body_anemia|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|alpha_Thalassemia|Hemoglobin_H_disease|not_provided": 1,
    "HEMOGLOBIN_TONOSHO": 1,
    "alpha_Thalassemia|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Heinz_body_anemia|Hemoglobin_H_disease|not_provided|HEMOGLOBIN_PETAH_TIKVA": 1,
    "HEMOGLOBIN_MOSELLA": 1,
    "alpha_Thalassemia|not_provided|HEMOGLOBIN_HOPKINS_2": 1,
    "HEMOGLOBIN_STRUMICA|HEMOGLOBIN_SERBIA": 1,
    "not_provided|HBA1-related_disorder|HEMOGLOBIN_TWIN_PEAKS": 1,
    "HEMOGLOBIN_MELUSINE": 1,
    "not_provided|HEMOGLOBIN_CHIAPAS": 1,
    "HEMOGLOBIN_NOUAKCHOTT": 1,
    "HEMOGLOBIN_J_(TONGARIKI)": 1,
    "not_specified|not_provided|HEMOGLOBIN_O_(BUGINESE-X)|HEMOGLOBIN_BUGINESE-X|HEMOGLOBIN_O_(OLIVIERE)|HEMOGLOBIN_OLIVIERE|HEMOGLOBIN_O_(INDONESIA)|alpha_Thalassemia": 1,
    "HEMOGLOBIN_OLEANDER": 1,
    "HEMOGLOBIN_UBE-4|not_provided": 1,
    "Heinz_body_anemia|Hemoglobin_H_disease|alpha_Thalassemia|Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|HBA1-related_disorder|not_provided": 1,
    "not_specified|not_provided|HEMOGLOBIN_J_(BIRMINGHAM)|HEMOGLOBIN_J_(MEERUT)": 1,
    "not_provided|not_specified|alpha_Thalassemia|HEMOGLOBIN_OWARI": 1,
    "HEMOGLOBIN_MALHACEN": 1,
    "HEMOGLOBIN_SASSARI|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_MONTEFIORE": 1,
    "HEMOGLOBIN_FUKUTOMI": 1,
    "HEMOGLOBIN_ST._CLAUDE": 1,
    "HEMOGLOBIN_JACKSON": 1,
    "Methemoglobinemia|_alpha_type|Erythrocytosis|_familial|_7|Hemoglobin_H_disease|alpha_Thalassemia|Heinz_body_anemia|not_provided|HEMOGLOBIN_TUNIS-BIZERTE": 1,
    "HEMOGLOBIN_YUDA": 1,
    "HEMOGLOBIN_QUESTEMBERT": 1,
    "not_provided|HBA1-related_disorder|alpha_Thalassemia": 1,
    "HEMOGLOBIN_CAEN": 1,
    "HEMOGLOBIN_PAVIE": 1,
    "HEMOGLOBIN_CHICAGO": 1,
    "Heinz_body_anemia|HEMOGLOBIN_TOYAMA": 1,
    "HEMOGLOBIN_ATTLEBORO": 1,
    "HEMOGLOBIN_TOKONAME": 1,
    "Erythrocytosis|_familial|_7|HEMOGLOBIN_ROUEN|HEMOGLOBIN_ETHIOPIA": 1,
    "HEMOGLOBIN_F_(KOELLIKER)|HEMOGLOBIN_KOELLIKER": 1,
    "HEMOGLOBIN_J_(CUBUJUQUI)": 1,
    "HEMOGLOBIN_J_(CAMAGUEY)": 1,
    "HEMOGLOBIN_NUNOBIKI|Erythrocytosis|_familial|_7": 1,
    "HEMOGLOBIN_SURESNES|Erythrocytosis|_familial|_7": 1,
    "not_provided|HEMOGLOBIN_SINGAPORE": 1,
    "HEMOGLOBIN_LEGNANO|Erythrocytosis|_familial|_7": 1,
    "LUC7L-related_disorder": 4,
    "AXIN1-related_disorder": 16,
    "not_provided|Hepatocellular_carcinoma|Caudal_duplication": 1,
    "Craniometadiaphyseal_osteosclerosis_with_hip_dysplasia": 2,
    "AXIN1-related_disorder|Caudal_duplication|Hepatocellular_carcinoma|not_provided": 1,
    "Hepatocellular_carcinoma|Craniometadiaphyseal_osteosclerosis_with_hip_dysplasia": 1,
    "not_provided|AXIN1-related_disorder": 4,
    "Hepatocellular_carcinoma|not_specified": 1,
    "Oculogastrointestinal-neurodevelopmental_syndrome": 9,
    "CAPN15-related_disorder": 26,
    "CAPN15-related_disorder|not_provided": 12,
    "not_specified|CAPN15-related_disorder": 3,
    "not_provided|CAPN15-related_disorder": 9,
    "CAPN15-related_disorder|not_specified": 1,
    "not_specified|Oculogastrointestinal-neurodevelopmental_syndrome": 3,
    "Oculogastrointestinal-neurodevelopmental_syndrome|not_provided": 1,
    "not_provided|Oculogastrointestinal-neurodevelopmental_syndrome": 1,
    "not_specified|not_provided|Oculogastrointestinal-neurodevelopmental_syndrome": 1,
    "CAPN15-related_disorder|Oculogastrointestinal-neurodevelopmental_syndrome|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_77|not_specified|not_provided": 9,
    "Epilepsy|Inborn_genetic_diseases": 23,
    "Developmental_and_epileptic_encephalopathy|_77|not_provided|not_specified|Epilepsy": 3,
    "Epilepsy|PIGQ-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_77|PIGQ-related_disorder": 1,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|_77|Inborn_genetic_diseases": 1,
    "Epilepsy|not_provided|PIGQ-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_77|not_provided|Inborn_genetic_diseases|Epilepsy": 1,
    "Inborn_genetic_diseases|Epilepsy|not_provided": 1,
    "Epilepsy|PIGQ-related_disorder": 6,
    "Developmental_and_epileptic_encephalopathy|_77|Epilepsy": 4,
    "Developmental_and_epileptic_encephalopathy|_77|not_provided|Epilepsy": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_77|Epilepsy": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_77|Inborn_genetic_diseases|Epilepsy|PIGQ-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Epilepsy": 6,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|_77": 3,
    "PIGQ-related_disorder|Epilepsy": 1,
    "Epilepsy|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_77|Epilepsy|Global_developmental_delay|Optic_atrophy|Intractable_seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_77": 11,
    "Inborn_genetic_diseases|Epilepsy|PIGQ-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_77|not_provided|Epilepsy|PIGQ-related_disorder": 2,
    "not_provided|Epilepsy|Inborn_genetic_diseases": 2,
    "Epilepsy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_77": 1,
    "not_provided|Epilepsy|PIGQ-related_disorder": 5,
    "Epilepsy|PIGQ-related_disorder|not_provided": 1,
    "PIGQ-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_77|Inborn_genetic_diseases|Epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|_77|Epilepsy|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_77|Inborn_genetic_diseases|not_provided|Epilepsy": 2,
    "PIGQ-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_77|not_provided": 3,
    "Epilepsy|not_specified|not_provided": 1,
    "not_provided|Epilepsy|Developmental_and_epileptic_encephalopathy|_77|PIGQ-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_77|Epilepsy|not_provided|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_77|Epilepsy": 1,
    "not_provided|PIGQ-related_disorder": 2,
    "Spinocerebellar_ataxia_48": 19,
    "STUB1-related_disorder": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_16": 22,
    "Spinocerebellar_ataxia_48|Autosomal_recessive_spinocerebellar_ataxia_16|not_provided": 3,
    "STUB1-related_disorder|not_provided": 2,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_16": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_16|not_provided|Spinocerebellar_ataxia_48|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Spinocerebellar_ataxia_48|Autosomal_recessive_spinocerebellar_ataxia_16": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_16|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_48": 1,
    "not_provided|STUB1-related_disorder": 1,
    "Spinocerebellar_ataxia_48|not_provided|Autosomal_recessive_spinocerebellar_ataxia_16": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_16|Spinocerebellar_ataxia_48|not_provided": 1,
    "Spinocerebellar_ataxia_48|not_provided": 3,
    "Spinocerebellar_ataxia_48|Autosomal_recessive_spinocerebellar_ataxia_16": 3,
    "not_provided|Spinocerebellar_ataxia_48": 2,
    "Spinocerebellar_ataxia_48|not_specified|not_provided": 1,
    "CCDC78-related_disorder|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 4,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 427,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|Inborn_genetic_diseases": 28,
    "not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 16,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided": 6,
    "Inborn_genetic_diseases|CCDC78-related_disorder|not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|CCDC78-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided": 2,
    "not_specified|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 25,
    "not_provided|not_specified|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 4,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_specified": 5,
    "not_specified|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 4,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided|CCDC78-related_disorder": 1,
    "CCDC78-related_disorder": 1,
    "CCDC78-related_disorder|not_specified|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_specified|not_provided": 4,
    "not_specified|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|CCDC78-related_disorder|not_provided": 1,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|CCDC78-related_disorder|not_specified": 1,
    "not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|Inborn_genetic_diseases": 2,
    "Centronuclear_myopathy|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "not_specified|not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 2,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|Inborn_genetic_diseases|not_specified": 1,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|CCDC78-related_disorder": 5,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|Inborn_genetic_diseases|Centronuclear_myopathy": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "not_provided|CCDC78-related_disorder|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_specified": 2,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|Centronuclear_myopathy": 1,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|Inborn_genetic_diseases|not_provided": 1,
    "CCDC78-related_disorder|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 2,
    "CCDC78-related_disorder|not_provided|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "CCDC78-related_disorder|Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided": 1,
    "Congenital_myopathy_with_internal_nuclei_and_atypical_cores|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_myopathy_with_internal_nuclei_and_atypical_cores": 1,
    "Pulmonary_arteriovenous_malformation": 1,
    "Cardiovascular_phenotype|LMF1-related_disorder": 1,
    "Cardiovascular_phenotype|Lipase_deficiency|_combined|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|LMF1-related_disorder": 2,
    "Cardiovascular_phenotype|not_provided|LMF1-related_disorder": 1,
    "not_provided|LMF1-related_disorder": 1,
    "Lipase_deficiency|_combined": 6,
    "not_provided|Lipase_deficiency|_combined|Cardiovascular_phenotype|LMF1-related_disorder": 1,
    "Lipase_deficiency|_combined|Cardiovascular_phenotype": 1,
    "Lipase_deficiency|_combined|Cardiovascular_phenotype|not_provided": 6,
    "Lipase_deficiency|_combined|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Lipase_deficiency|_combined": 4,
    "Cardiovascular_phenotype|Lipase_deficiency|_combined": 3,
    "LMF1-related_disorder|Cardiovascular_phenotype|not_provided": 3,
    "not_provided|Lipase_deficiency|_combined": 3,
    "not_provided|LMF1-related_disorder|Lipase_deficiency|_combined|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|LMF1-related_disorder|Cardiovascular_phenotype": 3,
    "not_provided|not_specified|Cardiovascular_phenotype|LMF1-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Lipase_deficiency|_combined": 1,
    "LMF1-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "LMF1-related_disorder": 6,
    "not_provided|not_specified|LMF1-related_disorder|Cardiovascular_phenotype": 1,
    "Lipase_deficiency|_combined|LMF1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "LMF1-related_disorder|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|LMF1-related_disorder": 1,
    "Lipase_deficiency|_combined|not_specified": 1,
    "Lipase_deficiency|_combined|not_specified|LMF1-related_disorder": 1,
    "LMF1-related_disorder|not_provided": 1,
    "Lipase_deficiency|_combined|Cardiovascular_phenotype|LMF1-related_disorder": 1,
    "not_provided|LMF1-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Lipase_deficiency|_combined|not_provided": 1,
    "not_provided|Lipase_deficiency|_combined|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|LMF1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Lipase_deficiency|_combined": 1,
    "Lipase_deficiency|_combined|not_provided|LMF1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Lipase_deficiency|_combined": 1,
    "not_provided|Cardiovascular_phenotype|LMF1-related_disorder": 1,
    "SOX8-related_disorder|not_provided": 5,
    "SOX8-related_disorder": 13,
    "not_provided|SOX8-related_disorder": 2,
    "not_specified|Aplasia_of_the_ovary": 1,
    "SSTR5-related_disorder|not_provided": 2,
    "SSTR5-related_disorder": 4,
    "not_provided|SSTR5-related_disorder": 3,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 730,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 25,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases": 75,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1224,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 169,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 83,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided": 23,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV": 164,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided|Idiopathic_generalized_epilepsy": 1,
    "not_specified|not_provided|CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 182,
    "CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6": 3,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6": 13,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|not_provided": 4,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder": 9,
    "not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder": 16,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 15,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 33,
    "not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases": 5,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|not_provided|Idiopathic_generalized_epilepsy": 11,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy": 48,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases": 13,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided": 49,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 6,
    "not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 53,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|not_provided|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 19,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 10,
    "CACNA1H-related_disorder": 12,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|not_provided": 5,
    "not_provided|CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 4,
    "Hyperaldosteronism|_familial|_type_IV": 12,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 9,
    "not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder|not_provided": 1,
    "not_provided|CACNA1H-related_disorder": 2,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified": 3,
    "not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 9,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified": 9,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 50,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy": 1,
    "not_provided|CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "CACNA1H-related_disorder|not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 2,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 17,
    "not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 2,
    "CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 3,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 5,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 2,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 19,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified": 5,
    "not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 10,
    "CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases": 2,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 19,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy": 3,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 15,
    "CACNA1H-related_disorder|not_provided": 1,
    "CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|not_provided": 4,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified": 7,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 1,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|not_provided": 2,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|CACNA1H-related_disorder": 2,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|See_cases": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|CACNA1H-related_disorder|Idiopathic_generalized_epilepsy": 3,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV": 2,
    "Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified|not_provided": 6,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified": 5,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 4,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified|not_provided": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 3,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|not_provided|Idiopathic_generalized_epilepsy": 2,
    "CACNA1H-related_disorder|not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified": 1,
    "See_cases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided": 1,
    "Focal_epilepsy": 3,
    "Breast_ductal_adenocarcinoma|not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified|not_provided": 2,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder|Idiopathic_generalized_epilepsy": 3,
    "not_specified|not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "not_provided|Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 2,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 9,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6": 7,
    "CACNA1H-related_disorder|Inborn_genetic_diseases": 1,
    "CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 8,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV": 3,
    "Inborn_genetic_diseases|not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 5,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|not_specified": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|not_provided": 4,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_6": 1,
    "CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 6,
    "Inborn_genetic_diseases|not_specified|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "CACNA1H-related_disorder|not_provided|not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|Inborn_genetic_diseases": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified|not_provided": 3,
    "CACNA1H-related_disorder|not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|not_provided|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 4,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|not_provided": 3,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 1,
    "CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6": 3,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|not_provided": 3,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6": 3,
    "not_specified|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_specified|CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 7,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|not_specified": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder|not_specified|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_6|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|See_cases|not_provided": 1,
    "Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases": 1,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified|CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|CACNA1H-related_disorder": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|not_specified|Idiopathic_generalized_epilepsy": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified|CACNA1H-related_disorder": 1,
    "CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|not_provided|Idiopathic_generalized_epilepsy": 2,
    "Inborn_genetic_diseases|CACNA1H-related_disorder": 1,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy": 2,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 7,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|CACNA1H-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "not_specified|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided": 5,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|not_provided|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified": 1,
    "not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6": 2,
    "not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided": 2,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified": 1,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 2,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 2,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified": 1,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified|not_provided": 2,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|not_specified": 1,
    "CACNA1H-related_disorder|not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV": 1,
    "Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified|not_provided": 1,
    "not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|CACNA1H-related_disorder": 1,
    "Hyperaldosteronism|_familial|_type_IV|Primary_aldosteronism|not_provided": 1,
    "CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy": 1,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 2,
    "Inborn_genetic_diseases|Increased_circulating_aldosterone_concentration|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|CACNA1H-related_disorder|Inborn_genetic_diseases": 1,
    "CACNA1H-related_disorder|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|See_cases|Idiopathic_generalized_epilepsy": 1,
    "not_specified|not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 1,
    "CACNA1H-related_disorder|not_provided|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified": 1,
    "not_specified|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided": 1,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_specified": 1,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV": 2,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided|Inborn_genetic_diseases|Increased_circulating_aldosterone_concentration": 1,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided": 3,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases|CACNA1H-related_disorder|Idiopathic_generalized_epilepsy": 1,
    "Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|not_provided|not_specified": 1,
    "not_specified|CACNA1H-related_disorder|Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Inborn_genetic_diseases|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided": 1,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|not_provided": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|CACNA1H-related_disorder|not_provided|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Hyperaldosteronism|_familial|_type_IV|not_specified|Epilepsy|_childhood_absence|_susceptibility_to|_6|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases": 1,
    "not_specified|CACNA1H-related_disorder|not_provided": 1,
    "not_provided|not_specified|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Inborn_genetic_diseases": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|CACNA1H-related_disorder|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "Inborn_genetic_diseases|not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_provided|Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_specified": 1,
    "Epilepsy|_childhood_absence|_susceptibility_to|_6|Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy": 1,
    "not_specified|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|not_provided": 1,
    "CACNA1H-related_disorder|Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|not_provided|Inborn_genetic_diseases": 1,
    "Idiopathic_generalized_epilepsy|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|Tremor|Hand_tremor|Cerebral_arteriovenous_malformation|Arteriovenous_malformation": 1,
    "Inborn_genetic_diseases|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified|Idiopathic_generalized_epilepsy": 1,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Idiopathic_generalized_epilepsy|Epilepsy|_childhood_absence|_susceptibility_to|_6|not_specified": 1,
    "not_provided|Hyperaldosteronism|_familial|_type_IV|Epilepsy|_childhood_absence|_susceptibility_to|_6": 1,
    "not_provided|not_specified|CACNA1H-related_disorder": 1,
    "BAIAP3-related_disorder": 1,
    "GNPTG-mucolipidosis|not_provided": 68,
    "GNPTG-mucolipidosis": 98,
    "GNPTG-mucolipidosis|GNPTG-related_disorder": 1,
    "GNPTG-related_disorder|not_specified|not_provided|GNPTG-mucolipidosis": 1,
    "not_provided|GNPTG-mucolipidosis": 66,
    "not_specified|GNPTG-mucolipidosis": 1,
    "GNPTG-related_disorder|GNPTG-mucolipidosis|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|GNPTG-mucolipidosis|not_specified": 2,
    "not_provided|GNPTG-mucolipidosis|Inborn_genetic_diseases": 2,
    "Retinal_dystrophy|not_provided|GNPTG-related_disorder|GNPTG-mucolipidosis": 1,
    "GNPTG-mucolipidosis|not_provided|Inborn_genetic_diseases": 4,
    "GNPTG-related_disorder|not_provided|GNPTG-mucolipidosis": 5,
    "Retinal_dystrophy|not_provided|GNPTG-mucolipidosis": 1,
    "GNPTG-related_disorder|not_provided": 1,
    "not_provided|not_specified|GNPTG-mucolipidosis": 1,
    "Inborn_genetic_diseases|not_provided|GNPTG-mucolipidosis": 2,
    "GNPTG-mucolipidosis|not_provided|not_specified": 2,
    "GNPTG-mucolipidosis|Mucolipidosis": 1,
    "Inborn_genetic_diseases|GNPTG-mucolipidosis|not_provided": 2,
    "Rod-cone_dystrophy|Retinal_dystrophy|GNPTG-mucolipidosis|not_provided": 1,
    "GNPTG-related_disorder|GNPTG-mucolipidosis|not_provided": 3,
    "Rod-cone_dystrophy|not_provided|GNPTG-mucolipidosis": 1,
    "GNPTG-mucolipidosis|not_provided|GNPTG-related_disorder": 1,
    "GNPTG-related_disorder": 1,
    "GNPTG-mucolipidosis|Inborn_genetic_diseases|not_provided": 1,
    "Retinal_dystrophy|not_specified|GNPTG-mucolipidosis|not_provided": 1,
    "Diarrhea_11|_malabsorptive|_congenital": 6,
    "not_specified|Osteopetrosis|not_provided": 2,
    "CLCN7-related_disorder": 7,
    "not_specified|not_provided|Osteopetrosis|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_osteopetrosis_2|not_provided|Autosomal_recessive_osteopetrosis_4": 1,
    "Autosomal_recessive_osteopetrosis_4|not_provided|Autosomal_dominant_osteopetrosis_2": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_4": 3,
    "Autosomal_dominant_osteopetrosis_2": 6,
    "not_provided|Autosomal_dominant_osteopetrosis_2": 3,
    "Autosomal_recessive_osteopetrosis_4|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_dominant_osteopetrosis_2|not_provided": 3,
    "Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2|not_provided": 1,
    "CLCN7-related_disorder|not_provided": 7,
    "not_provided|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_dominant_osteopetrosis_2|Autosomal_recessive_osteopetrosis_4": 2,
    "not_provided|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development": 1,
    "Autosomal_dominant_osteopetrosis_2|Autosomal_recessive_osteopetrosis_4|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|not_provided": 2,
    "not_provided|Increased_bone_mineral_density": 3,
    "Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_osteopetrosis_2|Autosomal_recessive_osteopetrosis_4|not_provided|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development": 2,
    "Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_4": 1,
    "CLCN7-related_disorder|not_provided|not_specified": 1,
    "not_provided|Osteopetrosis|not_specified": 3,
    "not_provided|Increased_bone_mineral_density|not_specified|Osteopetrosis": 1,
    "Autosomal_dominant_osteopetrosis_2|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_recessive_osteopetrosis_4|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Osteopetrosis": 3,
    "Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development": 1,
    "Autosomal_recessive_osteopetrosis_4|not_provided": 5,
    "Autosomal_dominant_osteopetrosis_2|not_provided": 1,
    "Autosomal_dominant_osteopetrosis_2|Autosomal_recessive_osteopetrosis_4": 1,
    "not_provided|Osteopetrosis|Increased_bone_mineral_density": 1,
    "Increased_bone_mineral_density|Autosomal_recessive_osteopetrosis_4|not_provided|Osteopetrosis|not_specified": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development": 2,
    "Autosomal_dominant_osteopetrosis_2|Autosomal_recessive_osteopetrosis_4|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Osteopetrosis|not_specified|not_provided": 1,
    "not_provided|Osteopetrosis|Inborn_genetic_diseases": 2,
    "Osteopetrosis|not_specified|not_provided": 2,
    "Autosomal_dominant_osteopetrosis_2|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_recessive_osteopetrosis_4": 1,
    "not_provided|Osteopetrosis|CLCN7-related_disorder": 1,
    "Autosomal_dominant_osteopetrosis_2|CLCN7-related_disorder": 1,
    "Autosomal_recessive_osteopetrosis_4|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Increased_bone_mineral_density|Osteopetrosis": 1,
    "CLCN7-related_disorder|Autosomal_dominant_osteopetrosis_2|Autosomal_recessive_osteopetrosis_4|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|not_provided": 1,
    "Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2|Abnormality_of_the_skeletal_system|Increased_bone_mineral_density|not_provided|CLCN7-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Increased_bone_mineral_density|Autosomal_dominant_osteopetrosis_2": 1,
    "Increased_bone_mineral_density|Osteopetrosis|not_provided": 3,
    "Osteopetrosis|not_provided|CLCN7-related_disorder": 3,
    "Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2|not_provided": 1,
    "Autosomal_dominant_osteopetrosis_2|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_recessive_osteopetrosis|not_provided": 1,
    "CLCN7-related_disorder|not_provided|Osteopetrosis": 1,
    "Autosomal_dominant_osteopetrosis_2|not_provided|CLCN7-related_disorder": 1,
    "CLCN7-related_disorder|Osteopetrosis|not_provided": 2,
    "not_provided|CLCN7-related_disorder": 2,
    "Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Autosomal_recessive_osteopetrosis_4": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2": 1,
    "Autosomal_recessive_osteopetrosis_4|Autosomal_dominant_osteopetrosis_2|not_specified|Hypopigmentation|_organomegaly|_and_delayed_myelination_and_development|Osteopetrosis|not_provided": 1,
    "Osteopetrosis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Osteopetrosis": 1,
    "Inborn_genetic_diseases|TELO2-related_intellectual_disability-neurodevelopmental_disorder|not_provided": 1,
    "TELO2-related_intellectual_disability-neurodevelopmental_disorder|not_provided|Inborn_genetic_diseases": 2,
    "TELO2-related_disorder": 2,
    "not_provided|TELO2-related_intellectual_disability-neurodevelopmental_disorder": 8,
    "not_provided|TELO2-related_disorder": 6,
    "TELO2-related_disorder|not_provided": 7,
    "TELO2-related_intellectual_disability-neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "TELO2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "TELO2-related_intellectual_disability-neurodevelopmental_disorder|not_provided": 10,
    "not_specified|TELO2-related_disorder|TELO2-related_intellectual_disability-neurodevelopmental_disorder|not_provided": 1,
    "TELO2-related_intellectual_disability-neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TELO2-related_intellectual_disability-neurodevelopmental_disorder|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|TELO2-related_intellectual_disability-neurodevelopmental_disorder": 1,
    "Saldino-Mainzer_syndrome": 1069,
    "not_provided|Saldino-Mainzer_syndrome": 30,
    "Retinitis_pigmentosa_80|not_provided|Saldino-Mainzer_syndrome": 3,
    "not_provided|not_specified|Saldino-Mainzer_syndrome": 2,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Inborn_genetic_diseases": 8,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 45,
    "Cleft_palate|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 244,
    "Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 19,
    "IFT140-related_disorder": 19,
    "Saldino-Mainzer_syndrome|not_provided": 16,
    "See_cases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|not_specified|IFT140-related_disorder|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Saldino-Mainzer_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa_80|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome|IFT140-related_disorder": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinal_dystrophy|not_provided": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinal_dystrophy": 11,
    "not_provided|IFT140-related_disorder|Saldino-Mainzer_syndrome|Inborn_genetic_diseases": 1,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder": 10,
    "IFT140-related_disorder|Saldino-Mainzer_syndrome": 14,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy": 16,
    "IFT140-related_disorder|Inborn_genetic_diseases|Saldino-Mainzer_syndrome": 2,
    "Retinal_ciliopathy_due_to_mutation_in_the_retinitis_pigmentosa-1_gene|Retinitis_pigmentosa_80": 1,
    "IFT140-related_disorder|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 3,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Saldino-Mainzer_syndrome": 36,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|not_provided": 12,
    "not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases": 3,
    "Saldino-Mainzer_syndrome|Joubert_syndrome_with_Jeune_asphyxiating_thoracic_dystrophy|Cranioectodermal_dysplasia|Cranioectodermal_dysplasia_5": 1,
    "Saldino-Mainzer_syndrome|Inborn_genetic_diseases": 15,
    "not_provided|Inborn_genetic_diseases|Saldino-Mainzer_syndrome": 3,
    "IFT140-related_disorder|Inborn_genetic_diseases|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 3,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome": 12,
    "Inborn_genetic_diseases|IFT140-related_disorder": 4,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|not_provided": 9,
    "Saldino-Mainzer_syndrome|Joubert_syndrome_with_Jeune_asphyxiating_thoracic_dystrophy": 1,
    "not_specified|not_provided|Saldino-Mainzer_syndrome": 5,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 6,
    "not_specified|not_provided|IFT140-related_disorder|Saldino-Mainzer_syndrome": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|not_provided|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Saldino-Mainzer_syndrome|not_specified|Retinitis_pigmentosa_80": 1,
    "not_specified|Saldino-Mainzer_syndrome": 4,
    "not_specified|not_provided|Asphyxiating_thoracic_dystrophy_1|Orofacial-digital_syndrome_III|Saldino-Mainzer_syndrome|Inborn_genetic_diseases|IFT140-related_disorder|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_80|not_provided": 1,
    "Jeune_thoracic_dystrophy|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases": 24,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|Retinitis_pigmentosa_80": 4,
    "Saldino-Mainzer_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa_80": 3,
    "not_provided|Saldino-Mainzer_syndrome|Inborn_genetic_diseases|Retinitis_pigmentosa_80": 1,
    "Microcephaly|Retinal_dystrophy|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|not_provided|Retinitis_pigmentosa_80": 2,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_80": 5,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 2,
    "IFT140-related_disorder|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 6,
    "Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinal_dystrophy|not_provided": 1,
    "not_provided|Saldino-Mainzer_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|IFT140-related_disorder|Saldino-Mainzer_syndrome": 1,
    "not_provided|Saldino-Mainzer_syndrome|IFT140-related_disorder": 1,
    "Saldino-Mainzer_syndrome|not_specified": 4,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|not_specified|Retinitis_pigmentosa_80|not_provided": 1,
    "Saldino-Mainzer_syndrome|not_provided|not_specified|Retinitis_pigmentosa_80": 1,
    "not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 6,
    "Retinitis_pigmentosa_80": 16,
    "Inborn_genetic_diseases|Retinal_dystrophy|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_80": 1,
    "not_provided|IFT140-related_disorder|Saldino-Mainzer_syndrome": 4,
    "not_provided|not_specified|Retinal_dystrophy|Saldino-Mainzer_syndrome": 1,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|IFT140-related_disorder|not_provided": 1,
    "IFT140-related_disorder|Retinal_dystrophy|Saldino-Mainzer_syndrome": 2,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|IFT140-related_disorder": 3,
    "Saldino-Mainzer_syndrome|not_provided|Joubert_syndrome_with_Jeune_asphyxiating_thoracic_dystrophy": 1,
    "Retinal_dystrophy|not_specified|Saldino-Mainzer_syndrome": 1,
    "Saldino-Mainzer_syndrome|not_specified|not_provided|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinal_dystrophy|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Retinal_dystrophy|Saldino-Mainzer_syndrome": 1,
    "IFT140-related_disorder|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinal_dystrophy": 2,
    "not_provided|Retinal_dystrophy|Saldino-Mainzer_syndrome": 2,
    "not_specified|Retinal_dystrophy|not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_80|Leber_congenital_amaurosis": 1,
    "Retinal_dystrophy|not_provided|Saldino-Mainzer_syndrome": 3,
    "Inborn_genetic_diseases|not_provided|Saldino-Mainzer_syndrome": 2,
    "Renal_cyst|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|not_specified|Retinitis_pigmentosa_80": 2,
    "Saldino-Mainzer_syndrome|Cranioectodermal_dysplasia_5|Polycystic_kidney_disease_9|_susceptibility_to|Retinitis_pigmentosa|Retinitis_pigmentosa_80|Retinal_dystrophy|IFT140-related_disorder": 1,
    "not_provided|IFT140-related_disorder": 1,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|not_provided": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|not_specified": 2,
    "IFT140-related_disorder|not_provided|Saldino-Mainzer_syndrome": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 2,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 3,
    "not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa|Retinitis_pigmentosa_80": 1,
    "IFT140-related_disorder|not_provided|Autosomal_dominant_polycystic_kidney_disease|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 1,
    "not_specified|Retinal_dystrophy|IFT140-related_disorder|Saldino-Mainzer_syndrome|not_provided": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinitis_pigmentosa": 1,
    "Cranioectodermal_dysplasia_5": 1,
    "IFT140-related_disorder|not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 2,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome|Microcephaly|not_provided": 1,
    "Inborn_genetic_diseases|Saldino-Mainzer_syndrome|IFT140-related_disorder": 2,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_80|Inborn_genetic_diseases|not_provided": 1,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|Retinitis_pigmentosa_80|Renal_cyst": 1,
    "Inborn_genetic_diseases|not_specified|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "not_provided|Saldino-Mainzer_syndrome|IFT140-related_disorder|Inborn_genetic_diseases|Retinitis_pigmentosa_80": 1,
    "Polycystic_kidney_disease_9|_susceptibility_to|IFT140-related_disorder|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Retinal_dystrophy|Renal_cyst|Polycystic_kidney_disease|not_provided|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|IFT140-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Retinal_dystrophy": 2,
    "not_specified|not_provided|Retinal_dystrophy|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Saldino-Mainzer_syndrome|Cranioectodermal_dysplasia": 1,
    "Saldino-Mainzer_syndrome|not_specified|not_provided|Nephronophthisis": 1,
    "not_provided|Saldino-Mainzer_syndrome|not_specified": 1,
    "Saldino-Mainzer_syndrome|See_cases|Retinitis_pigmentosa_80": 1,
    "not_specified|Retinal_dystrophy|Saldino-Mainzer_syndrome|not_provided|Retinitis_pigmentosa_80": 1,
    "IFT140-related_disorder|Polycystic_kidney_disease": 1,
    "Retinal_dystrophy|not_specified|not_provided|Saldino-Mainzer_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Saldino-Mainzer_syndrome": 1,
    "Optic_atrophy|Saldino-Mainzer_syndrome|not_provided": 1,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|not_provided": 1,
    "not_provided|Saldino-Mainzer_syndrome|IFT140-related_disorder|Retinitis_pigmentosa_80": 1,
    "Renal_cyst|IFT140-related_disorder|Retinitis_pigmentosa|not_provided": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Saldino-Mainzer_syndrome|IFT140-related_disorder": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Cranioectodermal_dysplasia_5|IFT140-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "IFT140-related_disorder|not_specified|not_provided|Saldino-Mainzer_syndrome": 2,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome|IFT140-related_disorder|Retinitis_pigmentosa_80": 1,
    "not_specified|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 2,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Cystic_renal_disease|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome": 1,
    "not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases|IFT140-related_disorder": 1,
    "Saldino-Mainzer_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Renal_cyst": 1,
    "IFT140-related_disorder|Retinitis_pigmentosa|IFT140-associated_disorder|Polycystic_kidney_disease_9|_susceptibility_to|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Renal_cyst": 1,
    "IFT140-related_disorder|not_specified|not_provided|Saldino-Mainzer_syndrome|Cleft_palate": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 2,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|IFT140-related_disorder": 1,
    "Saldino-Mainzer_syndrome|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_80": 1,
    "Retinitis_pigmentosa_80|IFT140-related_disorder": 1,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|IFT140-related_disorder": 1,
    "not_specified|Saldino-Mainzer_syndrome|Retinal_dystrophy|not_provided": 1,
    "Renal_cyst|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Retinitis_pigmentosa": 1,
    "IFT140-related_disorder|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Renal_cyst": 1,
    "Retinal_dystrophy|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Renal_cyst": 1,
    "Retinitis_pigmentosa_80|Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa|not_provided|Jeune_thoracic_dystrophy": 1,
    "IFT140-related_disorder|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Saldino-Mainzer_syndrome": 1,
    "Polycystic_kidney_disease_9|_susceptibility_to": 1,
    "Saldino-Mainzer_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Saldino-Mainzer_syndrome": 1,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|not_provided": 2,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|IFT140-related_disorder|Kidney_disorder": 1,
    "not_provided|Saldino-Mainzer_syndrome|Retinal_dystrophy|Retinitis_pigmentosa_80": 1,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Joubert_syndrome_with_Jeune_asphyxiating_thoracic_dystrophy|Jeune_thoracic_dystrophy|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa|IFT140-related_disorder|Retinitis_pigmentosa_80|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Saldino-Mainzer_syndrome": 1,
    "not_specified|Saldino-Mainzer_syndrome|not_provided": 1,
    "IFT140-related_disorder|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Retinal_ciliopathy_due_to_mutation_in_the_retinitis_pigmentosa-1_gene|Nephronophthisis|Jeune_thoracic_dystrophy|not_provided": 1,
    "IFT140-related_disorder|Inborn_genetic_diseases|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80": 1,
    "Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Asphyxiating_thoracic_dystrophy_1|IFT140-related_disorder": 1,
    "IFT140-related_disorder|not_provided|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|not_specified|not_provided": 1,
    "IFT140-related_disorder|not_specified|Saldino-Mainzer_syndrome|not_provided": 1,
    "not_provided|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Renal_cyst|Retinal_dystrophy": 1,
    "Saldino-Mainzer_syndrome|IFT140-related_disorder|not_provided|Retinitis_pigmentosa_80|not_specified": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Polycystic_kidney_disease_9|_susceptibility_to": 1,
    "IFT140-related_disorder|Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases": 1,
    "not_specified|Cranioectodermal_dysplasia_5": 1,
    "Retinitis_pigmentosa_80|Retinitis_pigmentosa|not_provided|Saldino-Mainzer_syndrome": 1,
    "not_provided|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|not_specified": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases|not_provided": 1,
    "Jeune_thoracic_dystrophy|Saldino-Mainzer_syndrome|not_provided": 1,
    "Saldino-Mainzer_syndrome|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Saldino-Mainzer_syndrome|Retinitis_pigmentosa_80|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "not_specified|Retinitis_pigmentosa_80|Saldino-Mainzer_syndrome|not_provided": 1,
    "not_provided|MAPK8IP3-related_disorder": 12,
    "MAPK8IP3-related_disorder": 31,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 8,
    "MAPK8IP3-related_disorder|not_provided": 6,
    "Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 64,
    "MAPK8IP3-related_disorder|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 1,
    "not_specified|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA|Inborn_genetic_diseases": 9,
    "MAPK8IP3-related_disorder|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA|not_provided": 4,
    "not_specified|not_provided|MAPK8IP3-related_disorder": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA|not_provided|Neurodevelopmental_disorder": 1,
    "not_provided|MAPK8IP3-related_disorder|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 2,
    "Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA|not_specified": 1,
    "not_provided|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 7,
    "MAPK8IP3-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|MAPK8IP3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA": 1,
    "Global_developmental_delay|2-3_finger_cutaneous_syndactyly": 1,
    "MAPK8IP3-related_disorder|Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA|not_provided": 1,
    "Neurodevelopmental_disorder_with_or_without_variable_brain_abnormalities%3B_NEDBA|not_provided|Inborn_genetic_diseases": 1,
    "NME3-related_condition": 1,
    "Combined_oxidative_phosphorylation_deficiency_32": 3,
    "MRPS34-related_disorder|not_provided": 7,
    "not_provided|MRPS34-related_disorder": 2,
    "MRPS34-related_disorder": 4,
    "MRPS34-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_32": 3,
    "Inborn_genetic_diseases|MRPS34-related_disorder": 1,
    "MRPS34-related_disorder|not_provided|Combined_oxidative_phosphorylation_deficiency_32": 1,
    "Combined_oxidative_phosphorylation_deficiency_32|not_provided|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_deficiency_32|Leigh_syndrome": 1,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency": 47,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 2,
    "IGFALS-related_disorder|Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_provided": 5,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_provided": 4,
    "IGFALS-related_disorder|not_provided": 1,
    "not_specified|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 2,
    "IGFALS-related_disorder": 4,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|Inborn_genetic_diseases": 5,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_specified|not_provided|IGFALS-related_disorder": 1,
    "not_provided|IGFALS-related_disorder|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 1,
    "not_provided|Short_stature_due_to_primary_acid-labile_subunit_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 6,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_provided": 1,
    "IGFALS-related_disorder|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 2,
    "not_specified|not_provided|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 1,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Short_stature_due_to_primary_acid-labile_subunit_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|IGFALS-related_disorder": 1,
    "IGFALS-related_disorder|not_provided|Short_stature_due_to_primary_acid-labile_subunit_deficiency": 1,
    "Short_stature_due_to_primary_acid-labile_subunit_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Premature_ovarian_failure_23": 1,
    "Spermatogenic_failure_22|Premature_ovarian_failure_23": 2,
    "Spermatogenic_failure_22": 3,
    "MEIOB-related_disorder": 6,
    "Spermatogenic_failure_22|Premature_ovarian_failure_23|not_provided": 1,
    "not_provided|MEIOB-related_disorder": 2,
    "Angioedema|_hereditary|_8": 2,
    "Cardiomyopathy|_dilated|_2D": 9,
    "Cardiomyopathy|_dilated|_2D|not_provided": 2,
    "not_specified|not_provided|Cardiomyopathy|_dilated|_2D": 1,
    "not_specified|Cardiomyopathy|_dilated|_2D": 1,
    "not_provided|Cardiomyopathy|_dilated|_2D": 2,
    "RPL3L-related_condition": 1,
    "NDUFB10-related_disorder|not_provided": 1,
    "Mitochondrial_complex_1_deficiency|_nuclear_type_35": 2,
    "GFER-related_disorder|not_specified|not_provided": 1,
    "not_provided|Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome": 7,
    "GFER-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome": 1,
    "Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome|not_provided|Mitochondrial_disease": 1,
    "Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome": 3,
    "GFER-related_disorder": 1,
    "Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome|not_provided": 2,
    "not_provided|Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|GFER-related_disorder": 2,
    "Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Mitochondrial_disease|not_provided|Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_cataract-progressive_muscular_hypotonia-hearing_loss-developmental_delay_syndrome": 1,
    "GFER-related_disorder|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3": 16,
    "not_provided|Familial_adenomatous_polyposis_3": 12,
    "not_provided|Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome": 36,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_3": 32,
    "NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|NTHL1-related_disorder|Familial_adenomatous_polyposis_3": 1,
    "Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome|not_provided": 35,
    "Familial_adenomatous_polyposis_3": 36,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_provided": 20,
    "Familial_adenomatous_polyposis_3|not_provided|Hereditary_cancer-predisposing_syndrome": 22,
    "Familial_adenomatous_polyposis_3|not_provided": 18,
    "not_provided|NTHL1-deficiency_tumor_predisposition_syndrome|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_specified": 1,
    "not_specified|not_provided|Familial_adenomatous_polyposis_3|NTHL1-related_disorder": 1,
    "NTHL1-related_disorder|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|NTHL1-related_disorder|Familial_adenomatous_polyposis_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_specified|not_provided|NTHL1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|NTHL1-related_disorder|not_provided": 1,
    "Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "not_provided|NTHL1-related_disorder|Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_provided|not_specified": 2,
    "NTHL1-related_disorder|not_provided|Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3": 9,
    "Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_3|not_provided|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "NTHL1-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome|not_specified|NTHL1-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_3|not_specified": 1,
    "Familial_adenomatous_polyposis_3|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_3|not_provided": 3,
    "Familial_adenomatous_polyposis_3|not_specified|Hereditary_cancer-predisposing_syndrome|NTHL1-related_disorder|not_provided": 1,
    "NTHL1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "NTHL1-deficiency_tumor_predisposition_syndrome": 2,
    "not_provided|not_specified|Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome": 1,
    "NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_3|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|NTHL1-related_disorder": 3,
    "not_provided|Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome|NTHL1-related_disorder": 2,
    "Familial_adenomatous_polyposis_3|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|NTHL1-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|NTHL1-related_disorder|not_provided": 1,
    "not_provided|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|NTHL1-related_disorder|Familial_adenomatous_polyposis_3|not_specified|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "not_provided|NTHL1-deficiency_tumor_predisposition_syndrome|Familial_adenomatous_polyposis_3|not_specified|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_specified|not_provided": 1,
    "NTHL1-related_disorder|Inherited_polyposis_and_early_onset_colorectal_cancer_-_germline_testing|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_adenomatous_polyposis_3": 1,
    "not_provided|Familial_adenomatous_polyposis_3|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_adenomatous_polyposis_3": 1,
    "NTHL1-deficiency_tumor_predisposition_syndrome|Familial_adenomatous_polyposis_3|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_adenomatous_polyposis_3": 1,
    "Familial_adenomatous_polyposis_3|NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_adenomatous_polyposis_3|NTHL1-related_disorder|not_provided|not_specified": 1,
    "NTHL1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_specified|NTHL1-related_disorder": 2,
    "NTHL1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome|NTHL1-related_disorder|not_provided": 1,
    "NTHL1-related_disorder|Familial_adenomatous_polyposis_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_adenomatous_polyposis_3|not_provided": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 168,
    "not_specified|TSC2-related_disorder": 1,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|TSC2-related_disorder": 1,
    "TSC2-related_disorder": 28,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 880,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 60,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 982,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 232,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 77,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 60,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 22,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 10,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 48,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 9,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 136,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 3,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 10,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_provided": 81,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 91,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 17,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified": 2,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 64,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 17,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 18,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 14,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 46,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided": 54,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 13,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 63,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 88,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 5,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 10,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 38,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 3,
    "Tuberous_sclerosis_2|not_specified": 42,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 22,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_syndrome|not_specified|Tuberous_sclerosis_2": 4,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 14,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Hypertrophic_cardiomyopathy_7|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2": 21,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 8,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 11,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Ovarian_cancer|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 23,
    "Autism_spectrum_disorder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Autism_spectrum_disorder|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 61,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 89,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 12,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Tuberous_sclerosis_2": 98,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 19,
    "not_specified|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_specified|Tuberous_sclerosis_2": 40,
    "TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 36,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 14,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 21,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 16,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 11,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 12,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 8,
    "not_provided|TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 12,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder": 1,
    "TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 18,
    "Tuberous_sclerosis_2|not_specified|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 2,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 9,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 3,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 3,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 3,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 15,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified": 3,
    "Tuberous_sclerosis_2|not_specified|not_provided": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|not_specified": 1,
    "not_specified|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 41,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 4,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 3,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 18,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 12,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 20,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 6,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 12,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|See_cases|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome": 2,
    "not_provided|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Autism_spectrum_disorder|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Focal_cortical_dysplasia|Cortical_tubers": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 6,
    "not_specified|not_provided|Tuberous_sclerosis_2": 3,
    "Tuberous_sclerosis_2|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_provided|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "not_specified|not_provided|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|Neoplasm_of_brain|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 8,
    "not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Seizure|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC2-related_disorder|not_specified|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|TSC2-related_disorder|not_specified|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 2,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 5,
    "Tuberous_sclerosis_2|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 5,
    "not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 19,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 2,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 2,
    "Tuberous_sclerosis_2|TSC2-related_disorder|not_provided": 2,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_specified": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided": 4,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 20,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_2|Seizure": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 18,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Intellectual_disability": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 11,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 6,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 2,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 2,
    "Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 3,
    "Tuberous_sclerosis_2|TSC2-related_disorder": 10,
    "Renal_cyst|Tuberous_sclerosis_2": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 4,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 16,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 7,
    "Tuberous_sclerosis_syndrome|not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 17,
    "Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 11,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 5,
    "Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 10,
    "not_specified|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 2,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis": 3,
    "Tuberous_sclerosis_2|Cortical_tubers|Hereditary_cancer-predisposing_syndrome|not_provided|Lymphangiomyomatosis": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|TSC2-related_disorder": 1,
    "TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 12,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 2,
    "Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "not_provided|not_specified|Tuberous_sclerosis_2": 3,
    "TSC2-related_disorder|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 5,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 3,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 2,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 5,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Autism_spectrum_disorder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 20,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 4,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|not_provided": 1,
    "not_specified|Tuberous_sclerosis_2|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided|not_specified": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|not_specified": 2,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|TSC2-related_disorder": 2,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 3,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified": 3,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 4,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_2|not_provided|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hirschsprung_disease|_susceptibility_to|_1|Tuberous_sclerosis_syndrome|not_provided|not_specified|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|not_provided": 2,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 6,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_specified": 2,
    "not_provided|Tuberous_sclerosis_2|not_specified": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|not_specified": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 19,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 4,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 2,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Dystonia|_early-onset|_and/or_spastic_paraplegia|not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_specified": 3,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified": 9,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 10,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 2,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|not_specified": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 2,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "not_provided|not_specified|Tuberous_sclerosis_syndrome": 3,
    "Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|TSC2-related_disorder|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 5,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|TSC2-related_disorder|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 4,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 2,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 2,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified": 1,
    "not_provided|Tuberous_sclerosis_syndrome|not_specified|Tuberous_sclerosis_2": 1,
    "not_specified|Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 4,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Intellectual_disability|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided": 1,
    "TSC2-related_disorder|not_specified|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_specified": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 3,
    "Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|not_specified": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|not_specified|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdomyoma|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|not_specified|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Epilepsy|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Renal_cyst": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided": 5,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 2,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Lung_lymphangioleiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|TSC2-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Dilated_cardiomyopathy_1D|not_provided": 1,
    "not_specified|TSC2-related_disorder|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_provided|TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 3,
    "not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|not_specified|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Autism_spectrum_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 2,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_specified": 1,
    "not_provided|Tuberous_sclerosis_syndrome|not_specified": 3,
    "Tuberous_sclerosis_1|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 3,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|TSC2-related_disorder|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_provided": 3,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Intellectual_disability|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 2,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "TSC2-related_disorder|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "not_specified|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 3,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 3,
    "not_specified|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Autism_spectrum_disorder|Tuberous_sclerosis_2": 1,
    "not_specified|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 2,
    "Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|TSC2-related_disorder|Tuberous_sclerosis_2": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 4,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder": 5,
    "not_specified|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_2|Bone_osteosarcoma": 1,
    "not_specified|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Neoplasm|Cortical_tubers|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_provided|not_specified|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Autism_spectrum_disorder|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 2,
    "Autism_spectrum_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_specified|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|not_provided": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Tuberous_sclerosis_2": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|not_provided": 2,
    "Cystic_fibrosis|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|not_specified": 1,
    "not_specified|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified|not_provided|Tuberous_sclerosis_2": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|TSC2-related_disorder": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 12,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 5,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 2,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|not_provided": 2,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_1|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|TSC2-related_disorder": 2,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder": 2,
    "Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided": 2,
    "not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2": 3,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder|not_provided|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 2,
    "TSC2-related_disorder|not_specified|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|not_provided": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|not_provided": 1,
    "not_provided|TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_specified|Tuberous_sclerosis_syndrome": 2,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|not_provided": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_provided|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder": 1,
    "Recurrent_fever|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_specified|not_provided|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Lung_lymphangioleiomyomatosis|not_specified|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 2,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 4,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_specified": 1,
    "TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Autism_spectrum_disorder|TSC2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder": 1,
    "TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "TSC2-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Seizure|Neurodevelopmental_delay|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 3,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|not_specified": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "not_provided|TSC2-related_disorder|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_1": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|See_cases": 1,
    "not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Autism_spectrum_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_specified": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_2": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 2,
    "not_specified|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 2,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder|not_specified|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 2,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Vesicoureteral_reflux_8|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Vascular_dementia": 1,
    "Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_specified|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided": 1,
    "Tuberous_sclerosis_syndrome|TSC2-related_disorder|See_cases": 1,
    "not_provided|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 2,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 2,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome": 1,
    "Lung_lymphangioleiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|not_specified": 1,
    "Tuberous_sclerosis_syndrome|Lung_lymphangioleiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 2,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|not_specified": 1,
    "Tuberous_sclerosis_syndrome|not_provided|not_specified|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 2,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "TSC2-related_disorder|not_provided|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "not_specified|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|not_provided": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|Infantile_spasms|Intellectual_disability|_severe|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|not_specified": 1,
    "not_provided|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_specified": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lymphangiomyomatosis|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Ovarian_cancer|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|not_specified": 1,
    "Autism_spectrum_disorder|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|TSC2-related_disorder|not_provided|Tuberous_sclerosis_2": 2,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome": 1,
    "not_provided|Tuberous_sclerosis_2|Intellectual_disability": 1,
    "not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Lung_lymphangioleiomyomatosis|not_specified|Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 4,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Everolimus_response|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Everolimus_response|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "not_specified|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_2": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_2": 3,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|TSC2-related_disorder|not_provided|Autism_spectrum_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "not_specified|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_2|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|See_cases|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Astroblastoma|_MN1-altered|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|not_specified": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Polycystic_kidney_disease|_adult_type": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|not_provided|Autism_spectrum_disorder|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|TSC2-related_disorder": 1,
    "Dental_enamel_pits|Hamartoma|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|not_provided": 1,
    "TSC2-related_disorder|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|not_specified|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|TSC2-related_disorder|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Joint_hypermobility|Tall_stature|Cafe-au-lait_spot|Arthralgia|Hyperextensible_hand_joints|Hyperextensibility_at_elbow": 1,
    "not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "TSC2-related_disorder|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "Tuberous_sclerosis_2|not_provided|Hereditary_cancer-predisposing_syndrome|TSC2-related_disorder": 1,
    "not_specified|Polycystic_kidney_disease|_adult_type": 31,
    "not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome": 1,
    "not_specified|Tuberous_sclerosis_2|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Polycystic_kidney_disease|_adult_type|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|TSC2-related_disorder": 1,
    "Polycystic_kidney_disease|_adult_type|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2|Lymphangiomyomatosis|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "TSC2-related_disorder|not_specified|not_provided|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "not_provided|TSC2-related_disorder|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Tuberous_sclerosis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Tuberous_sclerosis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|not_specified|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_2|Lymphangiomyomatosis|Isolated_focal_cortical_dysplasia_type_II|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Polycystic_kidney_disease|_adult_type": 1,
    "TSC2-related_disorder|Tuberous_sclerosis_2|not_specified": 1,
    "TSC2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "not_provided|TSC2-related_disorder|Tuberous_sclerosis_syndrome|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|not_specified": 1,
    "not_specified|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|TSC2-related_disorder": 1,
    "not_provided|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Tuberous_sclerosis_2|Tuberous_sclerosis_syndrome|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis": 1,
    "Tuberous_sclerosis_2|Hereditary_cancer-predisposing_syndrome|not_provided|TSC2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Lymphangiomyomatosis|Tuberous_sclerosis_and_lymphangiomyomatosis|not_provided|not_specified|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Isolated_focal_cortical_dysplasia_type_II|Tuberous_sclerosis_2": 1,
    "TSC2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2": 1,
    "Tuberous_sclerosis_syndrome|Abnormal_cerebral_morphology|Tuberous_sclerosis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder|Tuberous_sclerosis_syndrome": 1,
    "Tuberous_sclerosis_syndrome|not_provided|Tuberous_sclerosis_2|TSC2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|TSC2-related_disorder": 1,
    "not_provided|Tuberous_sclerosis_syndrome|Tuberous_sclerosis_2|not_specified": 1,
    "Lymphangiomyomatosis|Tuberous_sclerosis_syndrome|not_specified|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|not_specified|Autosomal_dominant_polycystic_kidney_disease": 1,
    "PKD1-related_disorder": 331,
    "Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder": 3,
    "Polycystic_kidney_disease|_adult_type|not_provided": 190,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 76,
    "Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases": 98,
    "not_specified|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases": 2,
    "Polycystic_kidney_disease|_adult_type|not_specified": 29,
    "not_specified|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 2,
    "not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 14,
    "not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 14,
    "PKD1-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type": 2,
    "not_specified|not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 3,
    "PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 63,
    "not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 14,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 31,
    "not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder": 2,
    "not_provided|Polycystic_kidney_disease|_adult_type": 231,
    "not_provided|PKD1-related_disorder": 28,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 3,
    "PKD1-related_disorder|not_provided": 26,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 3,
    "PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type|not_provided": 2,
    "not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_specified": 2,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|not_provided": 11,
    "Joubert_syndrome_10": 10,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 38,
    "PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease|Chronic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder|not_provided|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_provided": 3,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|not_provided": 9,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Inborn_genetic_diseases": 1,
    "PKD1-related_disorder|Inborn_genetic_diseases": 16,
    "not_specified|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease": 1,
    "not_provided|PKD1-related_disorder|Polycystic_kidney_disease": 3,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 13,
    "Polycystic_kidney_disease|PKD1-related_disorder": 9,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_provided": 11,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder|not_provided": 2,
    "not_provided|Polycystic_kidney_disease": 14,
    "not_provided|not_specified|PKD1-related_disorder": 2,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_provided": 2,
    "PKD1-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 3,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Renal_cyst|Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|Hyperechogenic_kidneys|Narrow_chest|Clubfoot|Polycystic_kidney_disease|_adult_type": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided": 4,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease": 22,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder|Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified|not_provided": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|not_specified|not_provided": 2,
    "not_provided|not_specified|Polycystic_kidney_disease|_adult_type": 7,
    "Polycystic_kidney_disease|_adult_type|not_provided|Autosomal_dominant_polycystic_kidney_disease|not_specified": 1,
    "not_specified|Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease": 7,
    "not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 13,
    "not_provided|not_specified|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|PKD1-related_disorder": 1,
    "not_provided|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 23,
    "not_provided|Tuberous_sclerosis_2|Isolated_focal_cortical_dysplasia_type_II|Lymphangiomyomatosis|Polycystic_kidney_disease|_adult_type": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|not_specified": 2,
    "Polycystic_kidney_disease|not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease|not_provided": 1,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type": 18,
    "not_specified|PKD1-related_disorder": 8,
    "not_provided|PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type": 2,
    "Polycystic_kidney_disease|_adult_type|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|PKD1-related_disorder": 16,
    "Polycystic_kidney_disease|not_specified": 6,
    "Polycystic_kidney_disease|PKD1-related_disorder|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|not_specified": 12,
    "not_specified|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided": 2,
    "Polycystic_kidney_disease|_adult_type|Hypertensive_disorder|Polycystic_kidney_disease|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder|not_specified": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_provided": 16,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|_adult_type": 13,
    "not_provided|Polycystic_kidney_disease|_adult_type|not_specified": 9,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 2,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided": 2,
    "PKD1-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|Polycystic_kidney_disease|not_specified": 1,
    "not_specified|Polycystic_kidney_disease": 3,
    "not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Polycystic_kidney_disease": 2,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|not_provided": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 2,
    "not_specified|Polycystic_kidney_disease|_adult_type|not_provided": 7,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 2,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified": 2,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "Renal_cyst|Polycystic_kidney_disease|_adult_type|not_provided": 1,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|not_provided|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Renal_cyst": 1,
    "Inborn_genetic_diseases|PKD1-related_disorder|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|not_specified": 4,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_specified": 3,
    "Polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 7,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_provided|not_specified": 1,
    "Renal_cyst|Polycystic_kidney_disease|_adult_type": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|not_provided|not_specified": 1,
    "Polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided": 1,
    "not_specified|Polycystic_kidney_disease|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|not_specified": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease": 7,
    "not_provided|not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 6,
    "not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_specified": 3,
    "not_provided|Polycystic_kidney_disease|PKD1-related_disorder|not_specified": 1,
    "not_provided|not_specified|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Polycystic_kidney_disease|Inborn_genetic_diseases": 1,
    "not_specified|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 3,
    "not_provided|Polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|Autosomal_dominant_polycystic_kidney_disease": 2,
    "not_provided|not_specified|Inborn_genetic_diseases|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease": 7,
    "PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease": 6,
    "not_specified|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|not_specified|not_provided": 1,
    "Polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 2,
    "Polycystic_kidney_disease|_adult_type|not_provided|Chronic_kidney_disease|not_specified": 1,
    "Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_(ADPKD)": 2,
    "PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_specified": 3,
    "Polycystic_kidney_disease|_adult_type|not_provided|Inborn_genetic_diseases": 8,
    "not_specified|not_provided|PKD1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "PKD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|Inborn_genetic_diseases|PKD1-related_disorder": 2,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_provided": 5,
    "Polycystic_kidney_disease|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 2,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 13,
    "not_specified|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_specified": 1,
    "PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_provided": 1,
    "PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided": 4,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease_2|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|PKD1-related_disorder|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder": 8,
    "Hepatic_cysts|Pancreatic_cysts|Renal_cyst|Renovascular_hypertension|Hypertensive_disorder": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease|not_provided|not_specified": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|Biliary_tract_abnormality": 1,
    "Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 7,
    "Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder|not_specified|not_provided": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease": 4,
    "PKD1-related_disorder|not_provided|not_specified": 2,
    "not_provided|not_specified|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|Polycystic_kidney_disease|not_provided": 2,
    "not_specified|Polycystic_kidney_disease|_adult_type|not_provided|Autosomal_dominant_polycystic_kidney_disease": 2,
    "not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 3,
    "Autosomal_dominant_polycystic_kidney_disease|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "not_provided|Polycystic_kidney_disease|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 1,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease": 3,
    "Polycystic_kidney_disease|_adult_type|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease": 2,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 3,
    "not_specified|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Inborn_genetic_diseases": 1,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "not_specified|not_provided|Polycystic_kidney_disease": 3,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease": 1,
    "not_provided|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_specified|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease|Multiple_renal_cysts|Hypertensive_disorder": 1,
    "not_specified|PKD1-related_disorder|not_provided": 3,
    "Polycystic_kidney_disease|_adult_type|Bile_duct_cancer|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "not_specified|not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_specified|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 2,
    "not_provided|not_specified|PKD1-related_disorder|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease|not_specified|not_provided": 2,
    "not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|not_provided": 3,
    "not_provided|Polycystic_kidney_disease|_adult_type|Congenital_anomaly_of_kidney_and_urinary_tract|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder|not_specified": 1,
    "not_provided|Kidney_failure|Polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder|not_specified": 1,
    "not_specified|Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|PKD1-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|PKD1-related_disorder": 2,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder": 4,
    "not_specified|not_provided|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease|_adult_type|Bile_duct_cancer|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified|not_provided": 1,
    "Renal_insufficiency": 1,
    "PKD1-related_disorder|not_specified": 2,
    "Polycystic_kidney_disease|_adult_type|not_provided|not_specified|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|not_specified|not_provided|Polycystic_kidney_disease": 1,
    "not_specified|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 2,
    "Polycystic_kidney_disease|_adult_type|not_specified|not_provided": 9,
    "Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Cystic_renal_disease|not_provided": 1,
    "Polycystic_kidney_disease_2|Polycystic_kidney_disease|_adult_type|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Lower_limb_muscle_weakness|Achilles_tendon_contracture|Lower_limb_amyotrophy|Elevated_circulating_creatine_kinase_concentration|not_provided": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|not_provided|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|PKD1-related_disorder": 2,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_provided|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|PKD1-related_disorder|not_provided|not_specified": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 4,
    "not_provided|Polycystic_kidney_disease|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "Narrow_chest|Clubfoot|Hyperechogenic_kidneys|Polycystic_kidney_disease|not_specified|not_provided": 1,
    "PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|Polycystic_kidney_disease|_adult_type": 3,
    "PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|not_specified": 3,
    "Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease|PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_provided": 1,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|not_provided|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 2,
    "Polycystic_kidney_disease|not_provided|PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Inborn_genetic_diseases": 2,
    "Polycystic_kidney_disease|_adult_type|not_provided|Autosomal_recessive_polycystic_kidney_disease": 1,
    "not_provided|not_specified|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Congenital_aneurysm_of_ascending_aorta": 1,
    "Polycystic_kidney_disease|not_specified|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|Polycystic_kidney_disease|PKD1-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 2,
    "Multiple_renal_cysts|Pancreatic_cysts|Hepatic_cysts": 1,
    "Inborn_genetic_diseases|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 5,
    "Inborn_genetic_diseases|not_provided|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 2,
    "PKD1-related_disorder|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "not_provided|Kidney_failure|Polycystic_kidney_disease|_adult_type": 1,
    "PKD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_recessive_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|Autosomal_dominant_polycystic_kidney_disease|not_provided|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|not_provided|not_specified|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease|not_specified|Renal_cyst|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|Cystic_renal_disease|Polycystic_liver_disease_1": 1,
    "not_provided|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_specified|Polycystic_kidney_disease|PKD1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "not_specified|Inborn_genetic_diseases|PKD1-related_disorder": 2,
    "not_provided|PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|not_specified|PKD1-related_disorder": 2,
    "not_specified|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease": 2,
    "not_provided|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_specified|PKD1-related_disorder": 1,
    "not_provided|Polycystic_kidney_disease|PKD1-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Renal_cyst": 3,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|not_provided|PKD1-related_disorder": 2,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Cystic_renal_dysplasia|Multicystic_kidney_dysplasia|Polycystic_liver_disease_1": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 1,
    "not_provided|not_specified|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Hereditary_ataxia|Autosomal_dominant_polycystic_kidney_disease|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|not_provided|PKD1-related_disorder|Inborn_genetic_diseases": 1,
    "PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder|Polycystic_kidney_disease|not_specified": 1,
    "not_specified|PKD1-related_disorder|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Inborn_genetic_diseases": 2,
    "Polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 2,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_specified|not_provided": 2,
    "PKD1-related_disorder|not_provided|not_specified|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|Renal_cyst|PKD1-related_disorder|Polycystic_liver_disease_1|Polycystic_kidney_disease": 1,
    "not_provided|PKD1-related_disorder|Inborn_genetic_diseases": 2,
    "Polycystic_kidney_disease|_adult_type|not_provided|Polycystic_kidney_disease|not_specified": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|not_specified|Inborn_genetic_diseases": 2,
    "not_specified|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Moderate_sensorineural_hearing_impairment|3-4_toe_syndactyly|not_provided": 1,
    "Polycystic_kidney_disease|not_provided|PKD1-related_disorder|not_specified": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder|not_specified": 1,
    "not_specified|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|Inborn_genetic_diseases": 2,
    "not_provided|PKD1-related_disorder|not_specified": 1,
    "not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Polycystic_kidney_disease|PKD1-related_disorder": 2,
    "Polycystic_kidney_disease|_adult_type|not_specified|not_provided|Polycystic_kidney_disease": 2,
    "Inborn_genetic_diseases|not_provided|PKD1-related_disorder": 2,
    "Renal_cyst|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "not_specified|PKD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_specified": 1,
    "PKD1-related_disorder|not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 4,
    "not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 6,
    "not_specified|not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Renal_insufficiency|Polycystic_kidney_disease|_adult_type": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "PKD1-related_disorder|not_specified|Inborn_genetic_diseases|Polycystic_kidney_disease|Multicystic_kidney_dysplasia|Abnormality_of_the_kidney|not_provided": 1,
    "not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|not_provided|PKD1-related_disorder|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|PKD1-related_disorder": 1,
    "PKD1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Hypertensive_disorder|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided": 1,
    "not_provided|PKD1-related_disorder|not_specified|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|PKD1-related_disorder|not_provided": 1,
    "not_provided|Polycystic_kidney_disease|PKD1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_specified|not_provided|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Bile_duct_cancer|not_specified": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|not_provided": 2,
    "Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|not_specified|Polycystic_kidney_disease": 2,
    "Polycystic_kidney_disease|PKD1-related_disorder|not_provided|not_specified": 1,
    "Polycystic_kidney_disease|_adult_type|not_provided|not_specified|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|not_provided|Polycystic_kidney_disease|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type": 1,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|_adult_type|not_provided": 1,
    "Renal_cyst|Proteinuria": 1,
    "not_provided|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|not_provided|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "PKD1-related_disorder|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|PKD1-related_disorder|not_specified|not_provided": 1,
    "Polycystic_liver_disease_1|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|Bladder_exstrophy-epispadias-cloacal_extrophy_complex|Polycystic_kidney_disease|PKD1-related_disorder|not_provided": 1,
    "Polycystic_kidney_disease|PKD1-related_disorder|Inborn_genetic_diseases|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease_3_with_or_without_polycystic_liver_disease|not_provided|Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Bile_duct_cancer": 1,
    "PKD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|not_provided|not_specified": 1,
    "Dilatation_of_the_cerebral_artery|Hepatic_cysts|Stage_5_chronic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases": 2,
    "Autosomal_dominant_polycystic_kidney_disease|not_specified|Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_provided|PKD1-related_disorder|Polycystic_kidney_disease": 1,
    "PKD1-related_disorder|not_provided|Polycystic_kidney_disease|_adult_type|not_specified|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_specified": 1,
    "See_cases|Polycystic_kidney_disease|_adult_type|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_polycystic_kidney_disease|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_specified|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|Polycystic_kidney_disease|not_provided": 1,
    "Polycystic_kidney_disease|_adult_type|Inborn_genetic_diseases|not_specified": 2,
    "PKD1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Polycystic_kidney_disease|_adult_type|not_provided|PKD1-related_disorder": 1,
    "not_provided|PKD1-related_disorder|Inborn_genetic_diseases|not_specified|Polycystic_kidney_disease": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type": 1,
    "Polycystic_kidney_disease|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|not_specified": 1,
    "PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|_adult_type|Autosomal_dominant_polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|Biliary_tract_abnormality": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease|PKD1-related_disorder": 1,
    "not_provided|Polycystic_kidney_disease|_adult_type|PKD1-Biallelic_Autosomal_Recessive_Polycystic_Kidney_Disease|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|Autosomal_dominant_polycystic_kidney_disease": 1,
    "not_specified|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_provided|Polycystic_kidney_disease": 1,
    "not_specified|not_provided|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "Polycystic_kidney_disease|_adult_type|PKD1-related_disorder|not_specified|not_provided|Polycystic_kidney_disease": 1,
    "not_specified|not_provided|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease|Enlarged_kidney|Hemangioma": 1,
    "Polycystic_kidney_disease|_adult_type|not_specified|Autosomal_dominant_polycystic_kidney_disease|not_provided": 1,
    "Atrial_septal_defect|_ostium_secundum_type|Polycystic_kidney_disease|Abnormal_nail_morphology|Abnormal_cortical_gyration|Hyperechogenic_kidneys|Missing_ribs|Dry_skin|Hemivertebrae|Periventricular_heterotopia|Plantar_crease_between_first_and_second_toes|Overlapping_fingers|Seizure|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "not_provided|Kidney_failure|not_specified|Polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Inborn_genetic_diseases|Autosomal_dominant_polycystic_kidney_disease": 1,
    "Polycystic_kidney_disease|Polycystic_kidney_disease|_adult_type|PKD1-related_disorder": 1,
    "Autosomal_dominant_polycystic_kidney_disease|not_provided|PKD1-related_disorder|not_specified|Polycystic_kidney_disease|_adult_type|Polycystic_kidney_disease": 1,
    "not_specified|PKD1-related_disorder|Polycystic_kidney_disease|_adult_type|not_provided|Autosomal_dominant_polycystic_kidney_disease": 1,
    "TRAF7-related_disorder|not_provided": 5,
    "not_provided|TRAF7-related_disorder": 4,
    "Inborn_genetic_diseases|TRAF7-related_disorder": 1,
    "TRAF7-related_disorder": 20,
    "not_provided|not_specified|TRAF7-related_disorder": 1,
    "not_provided|Cardiac|_facial|_and_digital_anomalies_with_developmental_delay": 3,
    "Cardiac|_facial|_and_digital_anomalies_with_developmental_delay|not_provided": 4,
    "TRAF7-related_disorder|Cardiac|_facial|_and_digital_anomalies_with_developmental_delay|not_provided": 1,
    "Laterality_defect_and_complex_congenital_heart_disease": 1,
    "not_provided|TRAF7-related_disorder|Cardiac|_facial|_and_digital_anomalies_with_developmental_delay": 1,
    "Cardiac|_facial|_and_digital_anomalies_with_developmental_delay|Inborn_genetic_diseases": 1,
    "TRAF7-associated_heart_defect-digital_anomalies-facial_dysmorphism-motor_and_speech_delay_syndrome|Cardiac|_facial|_and_digital_anomalies_with_developmental_delay": 1,
    "not_provided|TRAF7-related_syndrome|TRAF7-associated_heart_defect-digital_anomalies-facial_dysmorphism-motor_and_speech_delay_syndrome|Cardiac|_facial|_and_digital_anomalies_with_developmental_delay|Inborn_genetic_diseases": 1,
    "Complex_I_deficiency|not_provided": 1,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency": 130,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided|Hereditary_pulmonary_alveolar_proteinosis|not_specified": 2,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency": 10,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency": 18,
    "not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 19,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 42,
    "not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis": 3,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis|ABCA3-related_disorder": 2,
    "Hereditary_pulmonary_alveolar_proteinosis|ABCA3-related_disorder": 1,
    "Chromosome_22q11.2_deletion_syndrome|_distal|not_provided|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "ABCA3-related_disorder": 7,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 24,
    "Hereditary_pulmonary_alveolar_proteinosis|not_specified|not_provided": 2,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis|not_specified": 1,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis": 11,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_2": 1,
    "not_specified|Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided|ABCA3-related_disorder": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 12,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 5,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|not_specified|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 1,
    "not_provided|not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "ABCA3-related_disorder|not_specified|Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 1,
    "ABCA3-related_disorder|Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 5,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_2": 2,
    "ABCA3-related_disorder|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 3,
    "not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency": 2,
    "not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|ABCA3-related_disorder": 1,
    "Disorder_of_lung|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided|Hereditary_pulmonary_alveolar_proteinosis": 2,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|ABCA3-related_disorder": 3,
    "Interstitial_lung_disease_2|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 1,
    "not_provided|ABCA3-related_disorder": 2,
    "ABCA3-related_disorder|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|Congenital_hyperammonemia|_type_I": 1,
    "ABCA3-related_disorder|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "ABCA3-related_disorder|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "not_provided|not_specified|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis|not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency": 2,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|Interstitial_lung_disease_2|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 1,
    "ABCA3-related_disorder|not_provided": 3,
    "ABCA3-related_disorder|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis": 2,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|Abnormal_pulmonary_interstitial_morphology": 1,
    "ABCA3-related_disorder|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 3,
    "not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 3,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Recessive|not_provided": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_specified|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 2,
    "not_provided|ABCA3-related_disorder|not_specified|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "Interstitial_lung_disease_2|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "not_specified|ABCA3-related_disorder|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_specified": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|Primary_interstitial_lung_disease_specific_to_childhood_due_to_pulmonary_surfactant_protein_anomalies": 1,
    "not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 1,
    "Interstitial_lung_disease_2|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "Pulmonary_Surfactant_Metabolism_Dysfunction|_Recessive": 3,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided|not_specified": 2,
    "Primary_interstitial_lung_disease_specific_to_childhood_due_to_pulmonary_surfactant_protein_anomalies|Diffuse_interstitial_pulmonary_fibrosis": 1,
    "Respiratory_failure|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "ABCA3-related_disorder|not_provided|not_specified": 1,
    "Primary_interstitial_lung_disease_specific_to_childhood_due_to_pulmonary_surfactant_protein_anomalies|Diffuse_interstitial_pulmonary_fibrosis|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_2|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_provided|not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "Bullous_lung_disease|Hereditary_pulmonary_alveolar_proteinosis|not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_specified|ABCA3-related_disorder": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided": 1,
    "not_provided|not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|Hereditary_pulmonary_alveolar_proteinosis|ABCA3-related_disorder|not_specified": 1,
    "Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_specified|not_provided": 3,
    "ABCA3-related_disorder|not_provided|Hereditary_pulmonary_alveolar_proteinosis|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "not_provided|Hereditary_pulmonary_alveolar_proteinosis|Loeys-Dietz_syndrome|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "not_specified|Interstitial_lung_disease_due_to_ABCA3_deficiency|not_provided|ABCA3-related_disorder|Hereditary_pulmonary_alveolar_proteinosis": 1,
    "Interstitial_lung_disease_due_to_ABCA3_deficiency|Primary_interstitial_lung_disease_specific_to_childhood_due_to_pulmonary_surfactant_protein_anomalies|Hereditary_pulmonary_alveolar_proteinosis|not_provided": 1,
    "not_provided|Interstitial_lung_disease_due_to_ABCA3_deficiency|Interstitial_lung_disease_2": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_5": 9,
    "CCNF-related_disorder": 9,
    "not_specified|Amyotrophic_lateral_sclerosis": 1,
    "not_provided|CCNF-related_disorder": 1,
    "CCNF-related_disorder|not_provided": 2,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_5|not_specified": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_5|not_provided": 1,
    "Familial_infantile_myoclonic_epilepsy|not_provided": 11,
    "Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|DOORS_syndrome|Developmental_and_epileptic_encephalopathy|_16|Familial_infantile_myoclonic_epilepsy": 1,
    "Familial_infantile_myoclonic_epilepsy": 129,
    "Familial_infantile_myoclonic_epilepsy|not_specified": 1,
    "not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Familial_infantile_myoclonic_epilepsy|not_provided|not_specified": 1,
    "not_provided|not_specified|Familial_infantile_myoclonic_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 54,
    "Developmental_and_epileptic_encephalopathy|_16": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 7,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1": 46,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|TBC1D24-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1": 55,
    "not_specified|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 112,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 11,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided": 14,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 67,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 57,
    "Autosomal_recessive_nonsyndromic_hearing_loss_86": 9,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided": 4,
    "DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|Autosomal_dominant_nonsyndromic_hearing_loss_65|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16|Epilepsy|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided|TBC1D24-related_disorder": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided|DOORS_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided|Abnormality_of_the_nervous_system": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|DOORS_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 7,
    "not_specified|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Familial_infantile_myoclonic_epilepsy": 3,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 7,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|TBC1D24-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 6,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_provided": 3,
    "TBC1D24-related_disorder|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided": 11,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|not_provided": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_provided": 8,
    "TBC1D24-related_disorder|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 2,
    "not_specified|not_provided|Familial_infantile_myoclonic_epilepsy|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_86|DOORS_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 2,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_specified": 5,
    "Developmental_and_epileptic_encephalopathy|_16|Autosomal_dominant_nonsyndromic_hearing_loss_65|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Familial_infantile_myoclonic_epilepsy|not_provided|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Auditory_neuropathy_spectrum_disorder|Familial_infantile_myoclonic_epilepsy|Autosomal_recessive_nonsyndromic_hearing_loss_86|Autosomal_dominant_nonsyndromic_hearing_loss_65|DOORS_syndrome|Developmental_and_epileptic_encephalopathy|_16|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|not_provided": 1,
    "TBC1D24-related_disorder|not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Familial_infantile_myoclonic_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases": 6,
    "not_specified|TBC1D24-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided": 1,
    "Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1": 3,
    "TBC1D24-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 3,
    "TBC1D24-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|TBC1D24-related_disorder|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Familial_infantile_myoclonic_epilepsy|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_provided|DOORS_syndrome": 1,
    "TBC1D24-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Familial_infantile_myoclonic_epilepsy|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "not_provided|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_86|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "TBC1D24-related_disorder": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 3,
    "not_provided|TBC1D24-related_disorder": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Parkinsonian_disorder|Autosomal_dominant_epilepsy|DOORS_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Familial_infantile_myoclonic_epilepsy|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 8,
    "Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Developmental_and_epileptic_encephalopathy|_16|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|not_provided|not_specified": 1,
    "TBC1D24-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided|TBC1D24-related_disorder|Developmental_and_epileptic_encephalopathy|_16": 1,
    "not_specified|TBC1D24-related_disorder|not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases": 1,
    "Rare_genetic_deafness|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_16|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_16|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Familial_infantile_myoclonic_epilepsy|Autosomal_recessive_nonsyndromic_hearing_loss_86|Developmental_and_epileptic_encephalopathy|_16|DOORS_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided": 1,
    "not_provided|TBC1D24-related_disorder|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "not_provided|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases": 2,
    "Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified|not_provided": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|TBC1D24-related_disorder|Developmental_and_epileptic_encephalopathy|_16|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided|Inborn_genetic_diseases": 2,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|DOORS_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_nonsyndromic_hearing_loss_86|not_provided|DOORS_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases|not_provided": 4,
    "DOORS_syndrome|Familial_infantile_myoclonic_epilepsy|Malignant_migrating_partial_seizures_of_infancy|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|DOORS_syndrome|Familial_infantile_myoclonic_epilepsy|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|not_provided|Seizure|Cerebellar_atrophy|Specific_learning_disability|Movement_disorder|Global_developmental_delay": 1,
    "DOORS_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_65|Autosomal_recessive_nonsyndromic_hearing_loss_86|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 3,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_specified": 2,
    "DOORS_syndrome|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_86|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_86|Inborn_genetic_diseases": 1,
    "not_specified|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 4,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_specified|Inborn_genetic_diseases": 1,
    "Familial_infantile_myoclonic_epilepsy|Inborn_genetic_diseases|TBC1D24-related_disorder|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_16|not_provided": 1,
    "TBC1D24-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "TBC1D24-related_disorder|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_16|not_provided|DOORS_syndrome": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases": 2,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified": 4,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_nonsyndromic_hearing_loss_86|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16|DOORS_syndrome|Familial_infantile_myoclonic_epilepsy": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|Autosomal_dominant_nonsyndromic_hearing_loss_65|DOORS_syndrome|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "not_provided|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|TBC1D24-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Familial_infantile_myoclonic_epilepsy|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16|Autosomal_dominant_nonsyndromic_hearing_loss_65|DOORS_syndrome|Familial_infantile_myoclonic_epilepsy|Autosomal_recessive_nonsyndromic_hearing_loss_86|not_provided|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases": 1,
    "Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|TBC1D24-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|developmental_delay_with_seizures|not_specified|not_provided|DOORS_syndrome": 1,
    "Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome": 2,
    "Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_16|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_86|not_provided|TBC1D24-related_disorder": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|DOORS_syndrome|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_recessive_nonsyndromic_hearing_loss_86": 1,
    "Movement_disorder|Global_developmental_delay|Specific_learning_disability|Seizure|Cerebellar_atrophy": 1,
    "TBC1D24-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_provided|Nystagmus|Dysarthria|Seizure|Myoclonus|Tremor": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "DOORS_syndrome|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Familial_infantile_myoclonic_epilepsy|not_specified|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified": 3,
    "Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "TBC1D24-related_disorder|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_16|not_provided|DOORS_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|DOORS_syndrome|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16|Familial_infantile_myoclonic_epilepsy|Autosomal_recessive_nonsyndromic_hearing_loss_86|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_specified|Familial_infantile_myoclonic_epilepsy|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided|Inborn_genetic_diseases": 1,
    "Familial_infantile_myoclonic_epilepsy|not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Inborn_genetic_diseases": 1,
    "not_provided|Parkinsonian_disorder|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_16": 1,
    "not_provided|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome": 1,
    "Intellectual_disability|Periodic_paralysis|Neurodevelopmental_delay|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_16|Epilepsy|_progressive_myoclonic|_1B|Abnormality_of_the_nervous_system": 1,
    "Familial_infantile_myoclonic_epilepsy|not_specified|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_provided|Inborn_genetic_diseases": 1,
    "Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16|Familial_infantile_myoclonic_epilepsy|DOORS_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy|not_specified": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy|DOORS_syndrome|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1": 4,
    "Inborn_genetic_diseases|TBC1D24-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_16|Familial_infantile_myoclonic_epilepsy": 1,
    "Developmental_and_epileptic_encephalopathy|_16|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|TBC1D24-related_disorder": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_specified|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_86|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_16|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Familial_infantile_myoclonic_epilepsy|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|DOORS_syndrome|not_provided": 1,
    "Familial_infantile_myoclonic_epilepsy|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|DOORS_syndrome|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|TBC1D24-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy|Autosomal_recessive_nonsyndromic_hearing_loss_86|DOORS_syndrome|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Developmental_and_epileptic_encephalopathy|_16": 1,
    "TBC1D24-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_specified|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_16|DOORS_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Familial_infantile_myoclonic_epilepsy|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|TBC1D24-related_disorder|not_specified|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|DOORS_syndrome|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|not_provided": 1,
    "Inborn_genetic_diseases|Familial_infantile_myoclonic_epilepsy|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy": 2,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "not_provided|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|not_specified": 1,
    "TBC1D24-related_disorder|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|not_provided|Epilepsy|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1": 1,
    "TBC1D24-related_disorder|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy|not_provided|Inborn_genetic_diseases|DOORS_syndrome|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Autosomal_recessive_nonsyndromic_hearing_loss_86|Developmental_and_epileptic_encephalopathy|_16": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_65|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_16|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_specified": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_provided|Inborn_genetic_diseases": 1,
    "TBC1D24-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Familial_infantile_myoclonic_epilepsy": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Inborn_genetic_diseases|DOORS_syndrome|not_provided|Familial_infantile_myoclonic_epilepsy": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|not_specified": 1,
    "Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_86|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_16|Rolandic_epilepsy-paroxysmal_exercise-induced_dystonia-writer's_cramp_syndrome|DOORS_syndrome": 1,
    "Inborn_genetic_diseases|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Developmental_and_epileptic_encephalopathy|_1|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_provided": 1,
    "Inborn_genetic_diseases|TBC1D24-related_disorder|Familial_infantile_myoclonic_epilepsy|Developmental_and_epileptic_encephalopathy|_1|Caused_by_mutation_in_the_TBC1_domain_family|_member_24|Autosomal_dominant_nonsyndromic_hearing_loss_65|not_specified|not_provided": 1,
    "Familial_infantile_myoclonic_epilepsy|not_specified|not_provided": 1,
    "not_provided|Familial_infantile_myoclonic_epilepsy": 4,
    "Epilepsy|_early-onset|_3|_with_or_without_developmental_delay": 7,
    "EPILEPSY|_EARLY-ONSET|_3|_WITH_DEVELOPMENTAL_DELAY": 3,
    "not_provided|EPILEPSY|_EARLY-ONSET|_3|_WITH_DEVELOPMENTAL_DELAY": 2,
    "Childhood-onset_epilepsy_syndrome": 1,
    "EPILEPSY|_EARLY-ONSET|_3|_WITH_DEVELOPMENTAL_DELAY|Seizure": 1,
    "PDPK1-related_disorder": 3,
    "Intellectual_developmental_disorder|_autosomal_dominant_72": 23,
    "SRRM2-related_disorder": 21,
    "SRRM2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_dominant_72": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_72|Neurodevelopmental_disorder": 7,
    "SRRM2-related_Neurodevelopmental_disorder": 1,
    "not_provided|SRRM2-related_disorder": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_72": 1,
    "Status_epilepticus|Complex_febrile_seizure|Seizure": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_72|SRRM2-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_72|not_provided": 1,
    "Russell-Silver_syndrome|not_specified": 1,
    "Hearing_loss|_autosomal_recessive_116": 2,
    "CLDN9-related_disorder": 3,
    "not_specified|CLDN9-related_disorder": 1,
    "Hearing_loss|_autosomal_recessive_116|Hearing_loss": 1,
    "Hearing_loss|_autosomal_recessive_116|Nonsyndromic_genetic_hearing_loss": 1,
    "Pendred_syndrome|Hearing_loss|_autosomal_recessive_116": 1,
    "not_provided|CLDN9-related_disorder": 1,
    "THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|not_provided": 4,
    "THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome": 17,
    "THOC6-related_disorder": 5,
    "not_provided|THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome": 1,
    "Inborn_genetic_diseases|THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|not_provided": 1,
    "THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|not_provided|Dystonia|_early-onset|_and/or_spastic_paraplegia|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|THOC6-related_disorder": 2,
    "Inborn_genetic_diseases|THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome": 4,
    "not_provided|THOC6-related_disorder|THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|Intellectual_disability": 1,
    "THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|Dystonia|_early-onset|_and/or_spastic_paraplegia|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|THOC6-related_developmental_delay-microcephaly-facial_dysmorphism_syndrome|Dystonia|_early-onset|_and/or_spastic_paraplegia|not_provided|Intellectual_disability": 1,
    "Global_developmental_delay|ZSCAN10_Deficiency|Sensorineural_hearing_loss_disorder|Otofacial_neurodevelopmental_syndrome": 2,
    "Otofacial_neurodevelopmental_syndrome": 3,
    "Familial_Mediterranean_fever": 642,
    "not_provided|Familial_Mediterranean_fever": 27,
    "Familial_Mediterranean_fever|not_provided": 17,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided": 23,
    "not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis": 8,
    "MEFV-related_disorder|not_specified|Familial_Mediterranean_fever|not_provided|Autoinflammatory_syndrome": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_specified|not_provided": 1,
    "Acute_febrile_neutrophilic_dermatosis|Inborn_genetic_diseases|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "not_specified|Familial_Mediterranean_fever": 8,
    "Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant": 3,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|not_provided": 7,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis": 32,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 67,
    "not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|not_specified|Autoinflammatory_syndrome": 1,
    "Familial_Mediterranean_fever|not_specified": 15,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|not_provided|not_specified": 1,
    "Familial_Mediterranean_fever|Inborn_genetic_diseases": 11,
    "not_provided|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 3,
    "Inborn_genetic_diseases|Familial_Mediterranean_fever": 13,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_specified|not_provided": 2,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|not_specified|Dilated_cardiomyopathy_1A": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_provided": 8,
    "not_specified|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 3,
    "Familial_Mediterranean_fever|not_provided|not_specified": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_specified": 1,
    "Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|not_specified|MEFV-related_disorder|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|not_specified": 2,
    "Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever": 4,
    "Autoinflammatory_syndrome|not_specified|MEFV-related_disorder|not_provided|Familial_Mediterranean_fever": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|not_provided|not_specified": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_specified": 3,
    "not_specified|Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "not_specified|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Autoinflammatory_syndrome|Inborn_genetic_diseases|Familial_Mediterranean_fever": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 18,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 5,
    "Inborn_genetic_diseases|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided|not_specified": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_specified|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "MEFV-related_disorder": 12,
    "Heart|_malformation_of|Abnormal_cardiovascular_system_morphology|Renal_insufficiency|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Cachexia|Intermittent_diarrhea|Abnormality_of_the_dentition|Peripheral_neuropathy|Syncope|Urticaria": 1,
    "not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|not_provided": 2,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|Recurrent_fever": 1,
    "Autoinflammatory_syndrome|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided|not_specified|Familial_Mediterranean_fever": 2,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|See_cases": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|not_provided": 3,
    "Familial_Mediterranean_fever|_autosomal_dominant|not_provided|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 1,
    "Familial_Mediterranean_fever|Autoinflammatory_syndrome": 2,
    "not_specified|not_provided|Familial_Mediterranean_fever": 6,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Inborn_genetic_diseases": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified|not_provided": 3,
    "not_specified|Acute_febrile_neutrophilic_dermatosis|not_provided|Inborn_genetic_diseases|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Inborn_genetic_diseases|not_specified|Familial_Mediterranean_fever|not_provided": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided": 1,
    "MEFV-related_disorder|Familial_Mediterranean_fever": 3,
    "Inborn_genetic_diseases|not_provided|Familial_Mediterranean_fever": 3,
    "Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 4,
    "not_specified|Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided|Familial_Mediterranean_fever": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|Acute_febrile_neutrophilic_dermatosis|Inborn_genetic_diseases|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Familial_Mediterranean_fever|not_specified|not_provided": 3,
    "not_specified|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_Mediterranean_fever": 2,
    "not_specified|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|not_specified|Familial_Mediterranean_fever|not_provided": 1,
    "not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 5,
    "not_specified|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis": 4,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_specified|Acute_febrile_neutrophilic_dermatosis": 1,
    "Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|not_specified|not_provided|Familial_Mediterranean_fever": 1,
    "not_specified|Familial_Mediterranean_fever|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis": 3,
    "not_specified|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "not_provided|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Neurodevelopmental_delay|Skin_vesicle|Hyperpigmentation_of_the_skin": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Inborn_genetic_diseases": 2,
    "not_provided|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified": 1,
    "Familial_Mediterranean_fever|not_specified|Familial_Mediterranean_fever|_autosomal_dominant|not_provided": 1,
    "not_provided|Familial_Mediterranean_fever|_autosomal_dominant|not_specified|Familial_Mediterranean_fever": 1,
    "not_provided|not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant": 2,
    "Familial_Mediterranean_fever|_autosomal_dominant|not_provided|not_specified|Familial_Mediterranean_fever": 1,
    "not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 3,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|not_specified": 4,
    "Familial_Mediterranean_fever|_autosomal_dominant|not_specified|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 1,
    "MEFV-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Autoinflammatory_syndrome|not_specified": 1,
    "not_specified|Autoinflammatory_syndrome|Familial_Mediterranean_fever|not_provided|Inborn_genetic_diseases": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Autoinflammatory_syndrome|not_provided|Familial_Mediterranean_fever": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Inborn_genetic_diseases|Acute_febrile_neutrophilic_dermatosis": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "not_specified|Autoinflammatory_syndrome|Familial_Mediterranean_fever|Inborn_genetic_diseases": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Autoinflammatory_syndrome|not_specified|not_provided": 2,
    "not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Inborn_genetic_diseases|not_specified": 1,
    "Familial_Mediterranean_fever|not_specified|Autoinflammatory_syndrome|Inborn_genetic_diseases|Familial_Mediterranean_fever|_autosomal_dominant|not_provided": 1,
    "Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|not_specified|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified": 1,
    "Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|not_specified|Autoinflammatory_syndrome": 1,
    "not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_provided": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided|See_cases": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Central_core_myopathy|Familial_Mediterranean_fever": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_provided|Acute_febrile_neutrophilic_dermatosis|not_specified": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Familial_Mediterranean_fever": 4,
    "Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Autoinflammatory_syndrome": 1,
    "Behcet_disease|Familial_Mediterranean_fever|not_provided": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|not_specified|Familial_Mediterranean_fever": 2,
    "not_specified|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_provided|Behcet_disease": 1,
    "not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases|Familial_Mediterranean_fever": 2,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_provided": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_provided": 1,
    "See_cases|Familial_Mediterranean_fever": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_specified|not_provided": 4,
    "Familial_Mediterranean_fever|MEFV-related_disorder|Inborn_genetic_diseases": 1,
    "MEFV-related_disorder|Autoinflammatory_syndrome|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|not_specified|not_provided": 2,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Familial_Mediterranean_fever|not_provided|MEFV-related_disorder": 1,
    "Familial_Mediterranean_fever|not_specified|Autoinflammatory_syndrome|not_provided": 1,
    "MEFV-related_disorder|Autoinflammatory_syndrome|not_specified|not_provided|Familial_Mediterranean_fever": 2,
    "Familial_Mediterranean_fever|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever": 6,
    "MEFV-related_disorder|Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|not_provided|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|not_provided|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Acute_febrile_neutrophilic_dermatosis": 2,
    "Familial_Mediterranean_fever|Neuronal_ceroid_lipofuscinosis|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis": 1,
    "not_specified|Familial_Mediterranean_fever|Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided|MEFV-related_disorder": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_provided|Acute_febrile_neutrophilic_dermatosis": 1,
    "Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_specified": 1,
    "not_specified|not_provided|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Autoinflammatory_syndrome|Familial_Mediterranean_fever": 1,
    "Autoinflammatory_syndrome|not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Inborn_genetic_diseases|not_provided|Familial_Mediterranean_fever": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Autoinflammatory_syndrome|not_provided|MEFV-related_disorder|not_specified": 1,
    "not_specified|Autoinflammatory_syndrome": 1,
    "not_specified|Familial_Mediterranean_fever|not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|MEFV-related_disorder|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "Inborn_genetic_diseases|Familial_Mediterranean_fever|not_provided": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified": 1,
    "Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_provided|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified|Acute_febrile_neutrophilic_dermatosis": 1,
    "Familial_Mediterranean_fever|not_provided|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Autoinflammatory_syndrome|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Autoinflammatory_syndrome|not_provided": 1,
    "Acute_febrile_neutrophilic_dermatosis|not_specified|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "MEFV-related_disorder|Familial_Mediterranean_fever|not_provided": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|MEFV-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Systemic_lupus_erythematosus|See_cases": 1,
    "not_specified|Familial_Mediterranean_fever|_autosomal_dominant|not_provided|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever": 1,
    "not_specified|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 1,
    "Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|not_provided|not_specified": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_provided|not_specified|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|Familial_Mediterranean_fever": 1,
    "not_specified|Familial_Mediterranean_fever|Inborn_genetic_diseases": 1,
    "not_provided|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|not_provided|not_specified|Acute_febrile_neutrophilic_dermatosis|Inborn_genetic_diseases|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "MEFV-related_disorder|not_provided|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Autoinflammatory_syndrome|Familial_Mediterranean_fever": 1,
    "Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever": 1,
    "not_specified|Autoinflammatory_syndrome|Familial_Mediterranean_fever|Inborn_genetic_diseases|not_provided|MEFV-related_disorder|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_provided": 1,
    "not_specified|not_provided|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|_autosomal_dominant|MEFV-related_disorder": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_specified|Von_Hippel-Lindau_syndrome": 1,
    "Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|not_specified|not_provided": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Inborn_genetic_diseases|not_provided|not_specified|MEFV-related_disorder": 1,
    "Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|Inborn_genetic_diseases": 1,
    "not_provided|MEFV-related_disorder": 1,
    "Autoinflammatory_syndrome|Familial_Mediterranean_fever|not_specified|not_provided": 1,
    "Familial_Mediterranean_fever|MEFV-related_disorder|Autoinflammatory_syndrome": 1,
    "Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant|Acute_febrile_neutrophilic_dermatosis|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Familial_Mediterranean_fever|_autosomal_dominant|Familial_Mediterranean_fever|Acute_febrile_neutrophilic_dermatosis": 1,
    "MEFV-related_disorder|Autoinflammatory_syndrome|Familial_Mediterranean_fever|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "MEFV-related_disorder|Acute_febrile_neutrophilic_dermatosis|Familial_Mediterranean_fever|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "Basal_ganglia_calcification|_idiopathic|_9|_autosomal_recessive": 6,
    "CLUAP1-related_disorder|not_provided": 3,
    "not_provided|CLUAP1-related_disorder": 4,
    "Leber_congenital_amaurosis|Toriello-Lacassie-Droste_syndrome": 1,
    "Fanconi_anemia_complementation_group_P": 203,
    "Fanconi_anemia_complementation_group_P|not_provided": 2,
    "not_provided|Fanconi_anemia_complementation_group_P": 9,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_P": 2,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_P": 2,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia|Intellectual_disability": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia": 151,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P": 133,
    "SLX4-related_disorder|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 5,
    "Fanconi_anemia|not_specified|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_P": 1,
    "Fanconi_anemia_complementation_group_P|Inborn_genetic_diseases": 4,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_P": 12,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 3,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|Familial_cancer_of_breast|not_provided": 1,
    "SLX4-related_disorder|Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia": 3,
    "not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 16,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|Inborn_genetic_diseases": 10,
    "Fanconi_anemia_complementation_group_P|not_provided|Fanconi_anemia": 12,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 5,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_specified": 9,
    "SLX4-related_disorder|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 9,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_P": 10,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_provided": 2,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided": 13,
    "not_specified|SLX4-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|SLX4-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 10,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|Inborn_genetic_diseases": 6,
    "Fanconi_anemia|SLX4-related_disorder|Fanconi_anemia_complementation_group_P|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 7,
    "not_specified|Fanconi_anemia_complementation_group_P|not_provided|Fanconi_anemia": 3,
    "Fanconi_anemia|SLX4-related_disorder|Fanconi_anemia_complementation_group_P": 2,
    "not_provided|SLX4-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_P|Fanconi_anemia|SLX4-related_disorder": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A": 235,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|Hepatoblastoma": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Intellectual_disability": 1,
    "SLX4-related_disorder|Fanconi_anemia": 3,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "SLX4-related_disorder": 6,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|Olaparib_response": 1,
    "Fanconi_anemia_complementation_group_P|Inborn_genetic_diseases|Fanconi_anemia": 6,
    "Fanconi_anemia_complementation_group_P|not_provided|Fanconi_anemia|not_specified": 4,
    "Fanconi_anemia_complementation_group_P|SLX4-related_disorder|not_provided|Fanconi_anemia|not_specified": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 9,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided|not_specified": 4,
    "not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 5,
    "SLX4-related_disorder|not_provided|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|Inborn_genetic_diseases|SLX4-related_disorder": 1,
    "not_specified|Fanconi_anemia_complementation_group_P|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 3,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_specified|not_provided": 6,
    "Fanconi_anemia_complementation_group_P|Inborn_genetic_diseases|Fanconi_anemia|not_provided": 1,
    "not_specified|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_P": 3,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 2,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_specified": 2,
    "Fanconi_anemia|not_provided|not_specified|Fanconi_anemia_complementation_group_P": 6,
    "SLX4-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 1,
    "SLX4-related_disorder|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|SLX4-related_disorder|not_provided": 2,
    "Fanconi_anemia|SLX4-related_disorder": 9,
    "Inborn_genetic_diseases|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_specified|not_provided": 4,
    "Fanconi_anemia|SLX4-related_disorder|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|SLX4-related_disorder|not_specified|Fanconi_anemia_complementation_group_P|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided": 4,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_P": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_P": 7,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_P|SLX4-related_disorder": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|Inborn_genetic_diseases|not_specified": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_provided|not_specified": 3,
    "not_provided|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_P": 4,
    "SLX4-related_disorder|Fanconi_anemia_complementation_group_P|not_provided|Fanconi_anemia|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_P": 4,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_specified": 6,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_provided|Inborn_genetic_diseases": 1,
    "SLX4-related_disorder|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_P|not_provided|Fanconi_anemia|not_specified|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_P|not_provided": 2,
    "SLX4-related_disorder|not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 2,
    "not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_specified|not_provided": 2,
    "Fanconi_anemia|SLX4-related_disorder|not_specified|not_provided": 1,
    "SLX4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_P|Fanconi_anemia_complementation_group_A": 1,
    "SLX4-related_disorder|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_P": 1,
    "not_specified|SLX4-related_disorder|Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_P|not_provided|Fanconi_anemia|SLX4-related_disorder": 1,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_P|SLX4-related_disorder": 1,
    "SLX4-related_disorder|Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_specified": 1,
    "Microcephaly|Fanconi_anemia": 1,
    "SLX4-related_disorder|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|SLX4-related_disorder|not_specified": 2,
    "not_specified|SLX4-related_disorder|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|SLX4-related_disorder": 1,
    "not_specified|Fanconi_anemia_complementation_group_P|not_provided|SLX4-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_P|not_provided|not_specified|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia|not_provided": 2,
    "not_provided|SLX4-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|SLX4-related_disorder": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_P|not_provided": 4,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_provided|SLX4-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia_complementation_group_A|not_specified|not_provided|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_P": 1,
    "SLX4-related_disorder|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_P": 2,
    "Inborn_genetic_diseases|not_specified|Fanconi_anemia_complementation_group_P|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_P|Hereditary_cancer|not_specified|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_P": 2,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_P|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_P|not_specified": 1,
    "Glioblastoma_multiforme": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_specified|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_P|not_specified|not_provided|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_P|not_specified": 1,
    "Fanconi_anemia_complementation_group_P|Fanconi_anemia|not_specified|not_provided|SLX4-related_disorder": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia": 1,
    "SLX4-related_disorder|not_provided|Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_P|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Malignant_tumor_of_breast": 1,
    "not_provided|Fanconi_anemia_complementation_group_P|not_specified|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_P|SLX4-related_disorder": 1,
    "Fanconi_anemia|not_provided|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_P": 1,
    "DNASE1-related_disorder": 8,
    "not_provided|DNASE1-related_disorder": 2,
    "not_specified|Systemic_lupus_erythematosus|not_provided": 1,
    "not_specified|DNASE1-related_disorder|Systemic_lupus_erythematosus|_susceptibility_to": 1,
    "DNASE1-related_disorder|not_provided": 1,
    "TRAP1-related_disorder": 15,
    "TRAP1-related_disorder|HER2_positive_breast_carcinoma|not_provided": 1,
    "not_provided|TRAP1-related_disorder": 7,
    "TRAP1-related_disorder|not_specified": 2,
    "TRAP1-related_disorder|not_provided": 6,
    "not_provided|Hereditary_renal_cell_carcinoma": 1,
    "not_specified|TRAP1-related_disorder": 1,
    "TRAP1-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "TRAP1-related_disorder|not_provided|not_specified": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 303,
    "CREBBP-related_disorder": 222,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder": 67,
    "Rubinstein-Taybi_syndrome": 761,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 5,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 4,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_specified": 3,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 86,
    "Inborn_genetic_diseases|not_provided|CREBBP-related_disorder": 1,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 9,
    "CREBBP-related_disorder|not_provided|Rubinstein-Taybi_syndrome": 4,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 17,
    "Menke-Hennekam_syndrome_1": 20,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 23,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 3,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided|Rubinstein-Taybi_syndrome|not_specified|CREBBP-related_disorder|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 7,
    "Rubinstein-Taybi_syndrome|not_provided": 38,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 3,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_provided": 10,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 95,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome|not_provided|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 2,
    "Menke-Hennekam_syndrome_1|Inborn_genetic_diseases": 4,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 3,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|Hearing_impairment": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_specified": 2,
    "CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|not_provided": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|CREBBP-related_disorder": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 23,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 4,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 10,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided": 15,
    "Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided": 4,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases|CREBBP-related_disorder|not_provided": 1,
    "not_provided|Rubinstein-Taybi_syndrome": 23,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 14,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided": 1,
    "CREBBP-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "CREBBP-related_disorder|not_provided": 7,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided|CREBBP-related_disorder": 2,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder|not_specified": 1,
    "CREBBP-related_disorder|Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome": 5,
    "CREBBP-related_disorder|Inborn_genetic_diseases": 8,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|See_cases|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|not_provided|CREBBP-related_disorder|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder|not_specified": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|not_provided": 4,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_specified|not_provided": 3,
    "CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|not_provided": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|not_provided": 1,
    "not_specified|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_provided": 2,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder": 9,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder": 5,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases": 3,
    "Rubinstein-Taybi_syndrome|not_specified": 7,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|not_specified": 4,
    "not_specified|CREBBP-related_disorder": 4,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder": 3,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Menke-Hennekam_syndrome_1|CREBBP-related_disorder": 1,
    "Inborn_genetic_diseases|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided|Rubinstein-Taybi_syndrome": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_provided": 2,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 10,
    "Rubinstein-Taybi_syndrome|not_provided|CREBBP-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Scoliosis|Global_developmental_delay|not_provided": 1,
    "Rare_genetic_intellectual_disability|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided": 1,
    "Thumb_deformity|Morphological_central_nervous_system_abnormality|Spasticity|Spinal_dysraphism|Synophrys|Thin_vermilion_border": 1,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_specified": 3,
    "not_provided|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder": 2,
    "not_provided|CREBBP-related_disorder": 9,
    "See_cases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 2,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|Intellectual_disability|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 7,
    "Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_specified|not_provided": 2,
    "CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|CREBBP-related_disorder": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome": 10,
    "not_provided|CREBBP-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "CREBBP-related_disorder|not_provided|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 2,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|CREBBP-related_disorder": 2,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 4,
    "Rubinstein-Taybi_syndrome|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 4,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|Menke-Hennekam_syndrome_1": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_provided": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 13,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 2,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 9,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Tip-toe_gait": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|not_specified|not_provided": 1,
    "Rubinstein-Taybi_syndrome|not_provided|Inborn_genetic_diseases|CREBBP-related_disorder": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided": 5,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder|not_provided": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided|not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "not_specified|Menke-Hennekam_syndrome_1|not_provided|Rubinstein-Taybi_syndrome": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided|Intellectual_disability|CREBBP-related_disorder": 1,
    "not_provided|Menke-Hennekam_syndrome|Menke-Hennekam_syndrome_1|See_cases": 1,
    "not_provided|Rubinstein-Taybi_syndrome|Menke-Hennekam_syndrome_1": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_provided": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided": 2,
    "CREBBP-related_disorder|Neurodevelopmental_abnormality": 1,
    "Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided": 12,
    "Menke-Hennekam_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|Menke-Hennekam_syndrome_1|not_provided": 1,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Inborn_genetic_diseases": 6,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 3,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Rubinstein-Taybi_syndrome": 7,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Menke-Hennekam_syndrome_1|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided|Rubinstein-Taybi_syndrome": 1,
    "not_specified|not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Tip-toe_gait": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 2,
    "Inborn_genetic_diseases|CREBBP-related_disorder": 5,
    "Rubinstein-Taybi_syndrome|not_specified|not_provided": 4,
    "Rubinstein-Taybi_syndrome|not_provided|CREBBP-related_disorder": 3,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_specified": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_specified|not_provided": 2,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_specified|not_provided": 2,
    "not_provided|Rubinstein-Taybi_syndrome|CREBBP-related_disorder": 3,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder": 1,
    "CREBBP-related_disorder|not_specified|not_provided|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Neurodevelopmental_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 1,
    "CREBBP-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_provided": 3,
    "not_specified|not_provided|CREBBP-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|See_cases": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_specified": 3,
    "CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases|not_provided|Abnormality_of_the_nervous_system|Intellectual_disability": 1,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_provided|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|not_provided": 3,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|not_specified|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Glaucoma|Thumb_deformity|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|not_specified": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Kabuki-like_syndrome": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_specified": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Rubinstein-Taybi_syndrome": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_specified|not_provided|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases|not_specified": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 1,
    "Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_specified|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_specified": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided|CREBBP-related_disorder|not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Primary_ciliary_dyskinesia_3": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases": 1,
    "CREBBP-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|CREBBP-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided|not_specified": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Tip-toe_gait|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome|not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|not_provided": 1,
    "not_provided|CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Inborn_genetic_diseases|CREBBP-related_disorder|not_provided": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_specified": 1,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "not_specified|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_provided|Intellectual_disability": 1,
    "not_provided|CREBBP-related_disorder|Intellectual_disability|Rubinstein-Taybi_syndrome": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_provided|Rubinstein-Taybi_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|CREBBP-related_disorder": 1,
    "Rubinstein-Taybi_syndrome|not_specified|CREBBP-related_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|not_provided": 1,
    "not_provided|Congenital_heart_anomalies|Rubinstein-Taybi_syndrome": 1,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "not_provided|Rubinstein-Taybi_syndrome|not_specified": 1,
    "not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|CREBBP-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 3,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified|not_provided|CREBBP-related_disorder": 1,
    "Multiple_congenital_anomalies/dysmorphic_syndrome|CREBBP-related_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Marfanoid_habitus_and_intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided|Rubinstein-Taybi_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|CREBBP-related_disorder": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome": 2,
    "CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome|CREBBP-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Corpus_callosum|_agenesis_of": 1,
    "Inborn_genetic_diseases|CREBBP-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|not_provided|CREBBP-related_disorder|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_specified|not_provided": 1,
    "not_specified|CREBBP-related_disorder|Rubinstein-Taybi_syndrome": 1,
    "Inborn_genetic_diseases|CREBBP-related_disorder|not_specified|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|CREBBP-related_disorder|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|CREBBP-related_disorder|not_provided|Tip-toe_gait": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome": 1,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|not_provided": 1,
    "not_provided|CREBBP-related_disorder|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Hypertrophic_cardiomyopathy_11|Atrial_septal_defect_5|Left_ventricular_noncompaction_4|Dilated_cardiomyopathy_1R": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome|not_specified": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1|Rubinstein-Taybi_syndrome|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "CREBBP-related_disorder|not_provided|Abnormal_cerebral_morphology": 1,
    "CREBBP-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Rubinstein-Taybi_syndrome|not_provided|Inborn_genetic_diseases|See_cases": 1,
    "not_specified|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome|Tip-toe_gait|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_1": 1,
    "Nephronophthisis_7|not_specified|not_provided": 1,
    "not_provided|GLIS2-related_disorder": 1,
    "Nephronophthisis_7": 104,
    "Nephronophthisis|Nephronophthisis_7": 14,
    "Nephronophthisis|not_specified|not_provided|Nephronophthisis_7": 1,
    "Nephronophthisis_7|not_specified": 12,
    "not_specified|Nephronophthisis_7": 6,
    "not_specified|Nephronophthisis|not_provided|Nephronophthisis_7|Kidney_disorder": 1,
    "not_provided|not_specified|GLIS2-related_disorder|Nephronophthisis_7|Nephronophthisis": 1,
    "not_specified|Nephronophthisis|Nephronophthisis_7": 3,
    "GLIS2-related_disorder": 4,
    "Nephronophthisis|not_specified|Nephronophthisis_7": 3,
    "Nephronophthisis_7|Nephronophthisis|GLIS2-related_disorder": 1,
    "Nephronophthisis_7|GLIS2-related_disorder|Nephronophthisis": 2,
    "Nephronophthisis_7|not_provided": 2,
    "GLIS2-related_disorder|Nephronophthisis": 1,
    "Nephronophthisis_7|Nephronophthisis": 8,
    "GLIS2-related_disorder|Nephronophthisis_7": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_7|GLIS2-related_disorder|Kidney_disorder": 1,
    "Kidney_disorder|Nephronophthisis_7|Nephronophthisis": 1,
    "Nephronophthisis_7|Nephronophthisis|not_specified|not_provided": 1,
    "not_specified|Nephronophthisis_7|Nephronophthisis": 3,
    "Nephronophthisis|Nephronophthisis_7|not_specified": 1,
    "not_provided|Nephronophthisis|Nephronophthisis_7": 2,
    "not_provided|Kidney_disorder|Nephronophthisis|Nephronophthisis_7": 1,
    "Nephronophthisis|not_provided|GLIS2-related_disorder|Nephronophthisis_7|not_specified": 1,
    "Nephronophthisis|not_provided|not_specified|Nephronophthisis_7": 1,
    "Nephronophthisis_7|not_provided|Nephronophthisis": 1,
    "not_specified|GLIS2-related_disorder": 1,
    "Nephronophthisis|Nephronophthisis_7|not_specified|not_provided": 1,
    "GLIS2-related_disorder|not_specified|Nephronophthisis|not_provided|Nephronophthisis_7": 1,
    "not_provided|Nephronophthisis_7": 8,
    "Nephronophthisis|GLIS2-related_disorder|not_provided|Nephronophthisis_7": 1,
    "GLIS2-related_disorder|Nephronophthisis|Nephronophthisis_7": 1,
    "Nephronophthisis_7|Nephronophthisis|Kidney_disorder|not_specified|not_provided": 1,
    "not_provided|Nephronophthisis_7|Nephronophthisis|not_specified": 1,
    "Nephronophthisis|not_provided|Nephronophthisis_7|GLIS2-related_disorder": 1,
    "Nephronophthisis|GLIS2-related_disorder": 1,
    "Joubert_syndrome_20": 4,
    "not_provided|Kidney_disorder|Nephronophthisis_7": 1,
    "PAM16-related_disorder|not_provided": 1,
    "Autosomal_recessive_spondylometaphyseal_dysplasia|_Megarbane_type": 2,
    "not_provided|Autosomal_recessive_spondylometaphyseal_dysplasia|_Megarbane_type": 1,
    "ANKS3-related_disorder": 1,
    "not_provided|ANKS3-related_disorder": 1,
    "Spermatogenic_failure_10": 5,
    "SEPTIN12-related_disorder": 3,
    "not_provided|Spermatogenic_failure_10": 1,
    "not_specified|Spermatogenic_failure_10": 1,
    "Amelocerebrohypohidrotic_syndrome": 491,
    "Amelocerebrohypohidrotic_syndrome|not_provided": 18,
    "Amelocerebrohypohidrotic_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Amelocerebrohypohidrotic_syndrome": 12,
    "not_provided|Amelocerebrohypohidrotic_syndrome|Inborn_genetic_diseases": 1,
    "Amelocerebrohypohidrotic_syndrome|Inborn_genetic_diseases": 14,
    "not_provided|Amelocerebrohypohidrotic_syndrome|ROGDI-related_disorder": 3,
    "ROGDI-related_disorder|not_provided|Amelocerebrohypohidrotic_syndrome": 1,
    "Inborn_genetic_diseases|Amelocerebrohypohidrotic_syndrome": 21,
    "Amelocerebrohypohidrotic_syndrome|ROGDI-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Amelocerebrohypohidrotic_syndrome|not_provided": 2,
    "not_provided|not_specified|ROGDI-related_disorder|Amelocerebrohypohidrotic_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Amelocerebrohypohidrotic_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Amelocerebrohypohidrotic_syndrome": 1,
    "not_specified|Amelocerebrohypohidrotic_syndrome|not_provided": 1,
    "Amelocerebrohypohidrotic_syndrome|not_provided|ROGDI-related_disorder": 1,
    "Amelocerebrohypohidrotic_syndrome|not_specified|not_provided": 2,
    "Amelocerebrohypohidrotic_syndrome|ROGDI-related_disorder": 2,
    "ROGDI-related_disorder|Amelocerebrohypohidrotic_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|Amelocerebrohypohidrotic_syndrome": 2,
    "not_specified|not_provided|Amelocerebrohypohidrotic_syndrome": 1,
    "Amelocerebrohypohidrotic_syndrome|not_specified": 1,
    "ROGDI-related_disorder|Amelocerebrohypohidrotic_syndrome|not_provided": 1,
    "Amelocerebrohypohidrotic_syndrome|not_provided|not_specified": 1,
    "ROGDI-related_disorder": 3,
    "GLYR1-related_disorder": 2,
    "NAGPA-related_disorder": 10,
    "NAGPA-related_disorder|not_provided": 1,
    "Stuttering|_familial_persistent|_2|not_provided": 1,
    "Stuttering|_familial_persistent|_2": 1,
    "ALG1-congenital_disorder_of_glycosylation": 649,
    "ALG1-congenital_disorder_of_glycosylation|not_provided": 16,
    "Inborn_genetic_diseases|ALG1-congenital_disorder_of_glycosylation": 22,
    "ALG1-congenital_disorder_of_glycosylation|not_provided|Congenital_disorder_of_glycosylation": 4,
    "ALG1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 19,
    "not_provided|Inborn_genetic_diseases|ALG1-congenital_disorder_of_glycosylation": 1,
    "not_provided|ALG1-congenital_disorder_of_glycosylation|ALG1-related_disorder": 1,
    "not_provided|ALG1-congenital_disorder_of_glycosylation": 21,
    "not_specified|ALG1-congenital_disorder_of_glycosylation": 6,
    "ALG1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|ALG1-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|not_provided|ALG1-congenital_disorder_of_glycosylation": 3,
    "ALG1-congenital_disorder_of_glycosylation|not_provided|ALG1-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|ALG1-congenital_disorder_of_glycosylation|not_provided": 2,
    "ALG1-congenital_disorder_of_glycosylation|ALG1-related_disorder": 5,
    "ALG1-related_disorder|not_specified|not_provided|ALG1-congenital_disorder_of_glycosylation": 1,
    "ALG1-congenital_disorder_of_glycosylation|not_specified": 15,
    "ALG1-congenital_disorder_of_glycosylation|not_specified|not_provided": 4,
    "Congenital_disorder_of_glycosylation|ALG1-congenital_disorder_of_glycosylation": 10,
    "not_provided|ALG1-congenital_disorder_of_glycosylation|not_specified": 3,
    "not_specified|Inborn_genetic_diseases|ALG1-congenital_disorder_of_glycosylation": 1,
    "ALG1-related_disorder|ALG1-congenital_disorder_of_glycosylation": 9,
    "ALG1-related_disorder|ALG1-congenital_disorder_of_glycosylation|not_specified": 2,
    "not_provided|ALG1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "ALG1-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_specified|ALG1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|ALG1-congenital_disorder_of_glycosylation|ALG1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_disorder_of_glycosylation|Finnish_congenital_nephrotic_syndrome|ALG1-congenital_disorder_of_glycosylation|ALG12-congenital_disorder_of_glycosylation|Encephalopathy": 1,
    "not_specified|not_provided|Kabuki_syndrome_1|ALG1-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|ALG1-congenital_disorder_of_glycosylation|not_specified": 1,
    "ALG1-related_disorder": 5,
    "ALG1-congenital_disorder_of_glycosylation|not_provided|ALG1-related_disorder": 1,
    "ALG1-related_disorder|ALG1-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "ALG1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation": 1,
    "ALG1-related_disorder|not_provided|ALG1-congenital_disorder_of_glycosylation": 1,
    "not_provided|ALG1-related_disorder|ALG1-congenital_disorder_of_glycosylation": 2,
    "ALG1-congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation|not_provided": 2,
    "not_provided|Congenital_disorder_of_glycosylation|ALG1-congenital_disorder_of_glycosylation": 3,
    "Inborn_genetic_diseases|not_provided|Congenital_disorder_of_glycosylation|ALG1-congenital_disorder_of_glycosylation": 1,
    "not_specified|not_provided|ALG1-related_disorder|ALG1-congenital_disorder_of_glycosylation": 1,
    "not_specified|Congenital_disorder_of_glycosylation|ALG1-congenital_disorder_of_glycosylation": 1,
    "ALG1-related_disorder|Inborn_genetic_diseases|ALG1-congenital_disorder_of_glycosylation": 1,
    "not_provided|Encephalopathy|ALG1-congenital_disorder_of_glycosylation|ALG1-related_disorder|Congenital_disorder_of_glycosylation_type_I|Congenital_disorder_of_glycosylation": 1,
    "Congenital_disorder_of_glycosylation|not_provided|ALG1-congenital_disorder_of_glycosylation": 1,
    "Congenital_disorder_of_glycosylation|ALG1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_specified|ALG1-congenital_disorder_of_glycosylation|not_provided": 1,
    "RBFOX1-related_disorder": 5,
    "Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "Idiopathic_generalized_epilepsy|RBFOX1-related_disorder": 8,
    "not_provided|Idiopathic_generalized_epilepsy|RBFOX1-related_disorder": 1,
    "RBFOX1-related_disorder|Idiopathic_generalized_epilepsy": 3,
    "Intellectual_disability|_autosomal_dominant_46|Inborn_genetic_diseases|not_provided|Idiopathic_generalized_epilepsy": 1,
    "Idiopathic_generalized_epilepsy|Self-limited_epilepsy_with_centrotemporal_spikes": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Idiopathic_generalized_epilepsy": 2,
    "Idiopathic_generalized_epilepsy|RBFOX1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Idiopathic_generalized_epilepsy|Inborn_genetic_diseases|RBFOX1-related_disorder": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|RBFOX1-related_disorder|not_provided|Idiopathic_generalized_epilepsy": 1,
    "RBFOX1-related_disorder|not_specified|Idiopathic_generalized_epilepsy|not_provided": 1,
    "TMEM114-related_disorder": 2,
    "Gamma-aminobutyric_acid_transaminase_deficiency": 589,
    "Gamma-aminobutyric_acid_transaminase_deficiency|Inborn_genetic_diseases": 13,
    "Gamma-aminobutyric_acid_transaminase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "ABAT-related_disorder|not_specified|not_provided|Gamma-aminobutyric_acid_transaminase_deficiency": 2,
    "not_provided|Inborn_genetic_diseases|Gamma-aminobutyric_acid_transaminase_deficiency": 3,
    "Inborn_genetic_diseases|Gamma-aminobutyric_acid_transaminase_deficiency": 14,
    "not_provided|Gamma-aminobutyric_acid_transaminase_deficiency": 38,
    "ABAT-related_disorder|Gamma-aminobutyric_acid_transaminase_deficiency": 2,
    "Gamma-aminobutyric_acid_transaminase_deficiency|not_provided": 30,
    "Inborn_genetic_diseases|not_provided|Gamma-aminobutyric_acid_transaminase_deficiency": 1,
    "not_specified|not_provided|Gamma-aminobutyric_acid_transaminase_deficiency": 3,
    "ABAT-related_disorder|not_provided|Gamma-aminobutyric_acid_transaminase_deficiency": 1,
    "Gamma-aminobutyric_acid_transaminase_deficiency|not_specified": 1,
    "not_specified|Gamma-aminobutyric_acid_transaminase_deficiency": 5,
    "not_provided|ABAT-related_disorder|Gamma-aminobutyric_acid_transaminase_deficiency": 1,
    "Gamma-aminobutyric_acid_transaminase_deficiency|ABAT-related_disorder": 1,
    "ABAT-related_disorder": 1,
    "not_provided|Gamma-aminobutyric_acid_transaminase_deficiency|ABAT-related_disorder": 1,
    "PMM2-congenital_disorder_of_glycosylation|not_provided": 26,
    "PMM2-congenital_disorder_of_glycosylation": 567,
    "PMM2-related_disorder": 4,
    "PMM2-related_disorder|not_provided|PMM2-congenital_disorder_of_glycosylation": 2,
    "not_provided|PMM2-congenital_disorder_of_glycosylation": 44,
    "PMM2-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "PMM2-congenital_disorder_of_glycosylation|not_provided|not_specified": 2,
    "PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder": 6,
    "Inborn_genetic_diseases|PMM2-congenital_disorder_of_glycosylation|not_provided": 3,
    "PMM2-related_disorder|PMM2-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "not_specified|not_provided|PMM2-congenital_disorder_of_glycosylation": 3,
    "Inborn_genetic_diseases|PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|PMM2-congenital_disorder_of_glycosylation": 1,
    "not_specified|PMM2-congenital_disorder_of_glycosylation": 10,
    "PMM2-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PMM2-congenital_disorder_of_glycosylation": 6,
    "not_provided|PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder": 1,
    "not_provided|not_specified|PMM2-congenital_disorder_of_glycosylation": 2,
    "not_specified|PMM2-congenital_disorder_of_glycosylation|not_provided": 3,
    "PMM2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 9,
    "Intellectual_disability|not_provided|Inborn_genetic_diseases|PMM2-congenital_disorder_of_glycosylation": 1,
    "Premature_ovarian_failure|not_provided|PMM2-congenital_disorder_of_glycosylation": 1,
    "PMM2-congenital_disorder_of_glycosylation|not_provided|PMM2-related_disorder": 2,
    "Cerebral_palsy|Poor_speech|Spasticity|Cerebral_atrophy|Cerebellar_ataxia|Congenital_cerebellar_hypoplasia|PMM2-related_disorder|not_provided|PMM2-congenital_disorder_of_glycosylation": 1,
    "PMM2-related_disorder|PMM2-congenital_disorder_of_glycosylation": 4,
    "PMM2-congenital_disorder_of_glycosylation|not_specified": 8,
    "PMM2-related_disorder|Inborn_genetic_diseases|not_provided|PMM2-congenital_disorder_of_glycosylation": 2,
    "not_specified|PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder": 1,
    "Congenital_cerebellar_hypoplasia|not_provided|PMM2-congenital_disorder_of_glycosylation": 1,
    "PMM2-related_disorder|not_provided|Inborn_genetic_diseases|PMM2-congenital_disorder_of_glycosylation": 1,
    "Congenital_disorder_of_glycosylation_type_I|Cerebellar_ataxia|Cerebral_palsy|Poor_speech|Spasticity|Cerebral_atrophy|Congenital_cerebellar_hypoplasia|Diabetes_mellitus|Muscular_dystrophy|PMM2-related_disorder|Inborn_genetic_diseases|not_provided|Congenital_disorder_of_glycosylation|PMM2-congenital_disorder_of_glycosylation|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder|Inborn_genetic_diseases": 1,
    "PMM2-related_disorder|Inborn_genetic_diseases|not_provided|PMM2-congenital_disorder_of_glycosylation|See_cases": 2,
    "PMM2-congenital_disorder_of_glycosylation|See_cases": 1,
    "not_provided|PMM2-congenital_disorder_of_glycosylation|not_specified": 1,
    "PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder|not_specified": 1,
    "Cerebellar_ataxia|Muscular_dystrophy|Diabetes_mellitus|Congenital_cerebellar_hypoplasia|not_provided": 1,
    "PMM2-congenital_disorder_of_glycosylation|PMM2-related_disorder|not_provided": 1,
    "not_provided|PMM2-related_disorder|PMM2-congenital_disorder_of_glycosylation": 1,
    "not_provided|PMM2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|PMM2-congenital_disorder_of_glycosylation": 1,
    "not_provided|PMM2-congenital_disorder_of_glycosylation|Intellectual_disability|PMM2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|PMM2-related_disorder": 1,
    "PMM2-related_disorder|not_specified|PMM2-congenital_disorder_of_glycosylation": 1,
    "not_provided|USP7-related_disorder": 4,
    "Hao-Fountain_syndrome|not_provided": 5,
    "Hao-Fountain_syndrome_due_to_USP7_mutation": 14,
    "Hao-Fountain_syndrome": 31,
    "USP7-related_disorder": 10,
    "USP7-related_neurodevelopmental_disorder|not_provided": 1,
    "not_provided|not_specified|Hao-Fountain_syndrome": 1,
    "Hao-Fountain_syndrome|Inborn_genetic_diseases": 1,
    "Hao-Fountain_syndrome|Hypotonia": 1,
    "Hao-Fountain_syndrome|USP7-related_disorder": 2,
    "USP7-related_disorder|not_specified": 1,
    "not_provided|Hao-Fountain_syndrome_due_to_USP7_mutation": 1,
    "USP7-related_disorder|not_provided": 4,
    "USP7-related_neurodevelopmental_disorder": 1,
    "Landau-Kleffner_syndrome|not_provided": 140,
    "not_provided|Landau-Kleffner_syndrome": 109,
    "not_provided|Inborn_genetic_diseases|Landau-Kleffner_syndrome": 9,
    "Early-onset_epileptic_encephalopathy_and_intellectual_disability_due_to_GRIN2A_mutation|Landau-Kleffner_syndrome": 2,
    "Inborn_genetic_diseases|Landau-Kleffner_syndrome": 38,
    "Inborn_genetic_diseases|not_provided|Landau-Kleffner_syndrome": 4,
    "Intellectual_disability|Landau-Kleffner_syndrome": 5,
    "not_provided|GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome": 2,
    "Landau-Kleffner_syndrome|GRIN2A-related_complex_neurodevelopmental_disorder": 3,
    "Landau-Kleffner_syndrome|not_provided|Inborn_genetic_diseases": 8,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_specified|not_provided": 4,
    "Landau-Kleffner_syndrome|not_specified": 32,
    "Landau-Kleffner_syndrome|Inborn_genetic_diseases": 22,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome": 5,
    "Landau-Kleffner_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_specified": 2,
    "Complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome": 1,
    "Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_provided": 12,
    "GRIN2A-related_complex_neurodevelopmental_disorder|not_specified|Landau-Kleffner_syndrome|Inborn_genetic_diseases": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Landau-Kleffner_syndrome|Focal_epilepsy|not_specified|not_provided": 1,
    "Landau-Kleffner_syndrome|GRIN2A-related_complex_neurodevelopmental_disorder|not_provided": 2,
    "not_specified|Landau-Kleffner_syndrome": 28,
    "not_specified|not_provided|Landau-Kleffner_syndrome": 5,
    "not_specified|Landau-Kleffner_syndrome|Inborn_genetic_diseases": 2,
    "Landau-Kleffner_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "See_cases|Inborn_genetic_diseases|Landau-Kleffner_syndrome": 2,
    "GRIN2A-related_complex_neurodevelopmental_disorder": 6,
    "Landau-Kleffner_syndrome|Intellectual_disability": 4,
    "not_provided|Landau-Kleffner_syndrome|not_specified": 4,
    "Landau-Kleffner_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Landau-Kleffner_syndrome|not_provided": 4,
    "not_specified|Inborn_genetic_diseases|Landau-Kleffner_syndrome": 4,
    "Inborn_genetic_diseases|GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_specified|not_provided": 1,
    "Landau-Kleffner_syndrome|not_specified|Inborn_genetic_diseases": 2,
    "Epileptic_encephalopathy|Landau-Kleffner_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_specified|not_provided": 7,
    "Landau-Kleffner_syndrome|not_specified|not_provided": 5,
    "not_provided|Landau-Kleffner_syndrome|Inborn_genetic_diseases": 2,
    "GRIN2A-related_complex_neurodevelopmental_disorder|not_specified|Inborn_genetic_diseases|not_provided|Landau-Kleffner_syndrome": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_provided": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Landau-Kleffner_syndrome": 4,
    "Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_specified": 4,
    "Landau-Kleffner_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Landau-Kleffner_syndrome": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_provided|not_specified": 2,
    "Complex_neurodevelopmental_disorder|not_provided|Landau-Kleffner_syndrome": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Landau-Kleffner_syndrome|not_provided": 3,
    "Landau-Kleffner_syndrome|Inborn_genetic_diseases|not_provided|GRIN2A-related_complex_neurodevelopmental_disorder": 1,
    "Landau-Kleffner_syndrome|not_provided|See_cases": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_specified|not_provided": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|History_of_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_provided": 1,
    "Landau-Kleffner_syndrome|not_provided|Seizure": 2,
    "not_specified|Landau-Kleffner_syndrome|not_provided": 3,
    "Landau-Kleffner_syndrome|Epilepsy": 1,
    "Inborn_genetic_diseases|not_provided|Landau-Kleffner_syndrome|not_specified": 2,
    "Landau-Kleffner_syndrome|Neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder|not_provided|Landau-Kleffner_syndrome|Inborn_genetic_diseases": 1,
    "Dystonia|_intellectual_disability_and_language_impairment": 1,
    "Inborn_genetic_diseases|GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_provided": 1,
    "not_specified|Landau-Kleffner_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Landau-Kleffner_syndrome|Self-limited_epilepsy_with_centrotemporal_spikes": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Landau-Kleffner_syndrome": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Landau-Kleffner_syndrome": 1,
    "not_provided|Complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Landau-Kleffner_syndrome|not_provided|Seizure|Abnormal_cerebral_morphology": 1,
    "not_provided|not_specified|Landau-Kleffner_syndrome": 1,
    "not_specified|not_provided|Landau-Kleffner_syndrome|Inborn_genetic_diseases": 1,
    "Landau-Kleffner_syndrome|GRIN2A-related_complex_neurodevelopmental_disorder|not_provided|not_specified": 1,
    "GRIN2A-related_complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_provided": 2,
    "not_provided|GRIN2A-related_complex_neurodevelopmental_disorder|Landau-Kleffner_syndrome|not_specified": 1,
    "Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome": 64,
    "not_provided|GRIN2A-related_complex_neurodevelopmental_disorder": 2,
    "Landau-Kleffner_syndrome|not_specified|GRIN2A-related_complex_neurodevelopmental_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|GRIN2A-related_complex_neurodevelopmental_disorder|Inborn_genetic_diseases|Landau-Kleffner_syndrome|not_specified|not_provided": 1,
    "Landau-Kleffner_syndrome|Pyridoxine-dependent_epilepsy": 1,
    "EMP2-related_disorder": 5,
    "not_specified|not_provided|Nephrotic_syndrome|_type_10": 2,
    "not_provided|EMP2-related_disorder": 2,
    "Nephrotic_syndrome|_type_10|not_provided": 2,
    "EMP2-related_disorder|not_provided": 2,
    "not_provided|Nephrotic_syndrome|_type_10|not_specified": 1,
    "Nephrotic_syndrome|_type_10": 4,
    "MHC_class_II_deficiency|Inborn_genetic_diseases": 37,
    "Inborn_genetic_diseases|MHC_class_II_deficiency": 40,
    "CIITA-related_disorder|MHC_class_II_deficiency": 10,
    "CIITA-related_disorder": 3,
    "MHC_class_II_deficiency|Rheumatoid_arthritis": 10,
    "MHC_class_II_deficiency_1|Rheumatoid_arthritis|MHC_class_II_deficiency": 2,
    "MHC_class_II_deficiency|Rheumatoid_arthritis|MHC_class_II_deficiency_1|not_provided|Inborn_genetic_diseases": 1,
    "MHC_class_II_deficiency|Rheumatoid_arthritis|MHC_class_II_deficiency_1": 3,
    "CIITA-related_disorder|MHC_class_II_deficiency|not_provided": 3,
    "Rheumatoid_arthritis|MHC_class_II_deficiency_1": 3,
    "Rheumatoid_arthritis|MHC_class_II_deficiency_1|MHC_class_II_deficiency": 1,
    "CIITA-related_disorder|not_provided|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency|MHC_class_II_deficiency_1|Rheumatoid_arthritis": 2,
    "MHC_class_II_deficiency|not_provided|not_specified": 7,
    "MHC_class_II_deficiency_1|Rheumatoid_arthritis|MHC_class_II_deficiency|CIITA-related_disorder": 1,
    "Rheumatoid_arthritis|MHC_class_II_deficiency|Inborn_genetic_diseases|MHC_class_II_deficiency_1": 1,
    "Inborn_genetic_diseases|not_provided|MHC_class_II_deficiency": 1,
    "not_specified|MHC_class_II_deficiency|Rheumatoid_arthritis|MHC_class_II_deficiency_1": 1,
    "Rheumatoid_arthritis|MHC_class_II_deficiency": 2,
    "not_provided|CIITA-related_disorder|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency|CIITA-related_disorder": 7,
    "MHC_class_II_deficiency|CIITA-related_disorder|not_provided": 1,
    "MHC_class_II_deficiency_1|MHC_class_II_deficiency": 2,
    "Inborn_genetic_diseases|not_specified|MHC_class_II_deficiency": 1,
    "CIITA-related_disorder|MHC_class_II_deficiency|not_provided|not_specified": 1,
    "MHC_class_II_deficiency|Inborn_genetic_diseases|Rheumatoid_arthritis": 2,
    "MHC_class_II_deficiency|Inborn_genetic_diseases|CIITA-related_disorder": 1,
    "MHC_class_II_deficiency|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|MHC_class_II_deficiency|Rheumatoid_arthritis": 1,
    "MHC_class_II_deficiency_1|Rheumatoid_arthritis|not_provided|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_1|Rheumatoid_arthritis": 1,
    "Hodgkin_lymphoma|_susceptibility_to": 1,
    "MHC_class_II_deficiency|Rheumatoid_arthritis|MHC_class_II_deficiency_1|Inborn_genetic_diseases": 1,
    "MHC_class_II_deficiency|Rheumatoid_arthritis|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|MHC_class_II_deficiency": 1,
    "not_provided|MHC_class_II_deficiency|Rheumatoid_arthritis": 1,
    "not_provided|Autoinflammatory_syndrome_with_immunodeficiency": 2,
    "Autoinflammatory_syndrome_with_immunodeficiency": 11,
    "Autoinflammatory_syndrome_with_immunodeficiency|Autoimmune_thrombocytopenia|Autoimmune_hemolytic_anemia|not_provided": 2,
    "AUTOINFLAMMATORY_SYNDROME|_FAMILIAL|_WITHOUT_IMMUNODEFICIENCY|Systemic_lupus_erythematosus": 2,
    "AUTOINFLAMMATORY_SYNDROME|_FAMILIAL|_WITHOUT_IMMUNODEFICIENCY|Autoimmune_thrombocytopenic_purpura": 1,
    "Autoinflammatory_syndrome_with_immunodeficiency|not_specified": 1,
    "SOCS1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_1C": 136,
    "Charcot-Marie-Tooth_disease_type_1C|not_provided": 11,
    "not_provided|Charcot-Marie-Tooth_disease_type_1C": 10,
    "LITAF-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1C|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_1C|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_1C|Inborn_genetic_diseases": 9,
    "Charcot-Marie-Tooth_disease_type_1C|Charcot-Marie-Tooth_disease": 4,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1C": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1C": 10,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1C": 6,
    "LITAF-related_disorder": 1,
    "LITAF-related_disorder|not_provided": 2,
    "not_specified|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Charcot-Marie-Tooth_disease_type_1C|not_specified|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1C|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1C|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1C": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_1C|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1C|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1C|not_provided|not_specified": 1,
    "not_specified|Hereditary_ataxia|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Charcot-Marie-Tooth_disease_type_1C|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_1C|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_1C": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_1C|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_1C|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_1C|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_1C|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Charcot-Marie-Tooth_disease_type_1C|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_1C": 1,
    "Desmoplastic_small_round_cell_tumor": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 60,
    "Fanconi_anemia_complementation_group_Q": 12,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 143,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F": 118,
    "not_provided|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 5,
    "Xeroderma_pigmentosum|_group_F": 97,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Inborn_genetic_diseases|XFE_progeroid_syndrome|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Inborn_genetic_diseases": 5,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 53,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|not_provided|not_specified": 2,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|XFE_progeroid_syndrome": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 4,
    "not_provided|Behavioral_variant_of_frontotemporal_dementia|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 47,
    "XFE_progeroid_syndrome": 4,
    "Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|not_specified|Cockayne_syndrome|Xeroderma_pigmentosum|ERCC4-related_disorder": 1,
    "Xeroderma_pigmentosum|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F": 2,
    "Ovarian_cancer|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|not_provided": 3,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|Xeroderma_pigmentosum|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F": 1,
    "not_provided|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Cockayne_syndrome|not_specified": 1,
    "Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F": 13,
    "not_specified|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided|XFE_progeroid_syndrome": 1,
    "Xeroderma_pigmentosum|ERCC4-related_disorder|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|not_provided|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_specified|not_provided|Xeroderma_pigmentosum": 2,
    "not_provided|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 2,
    "Xeroderma_pigmentosum|_group_F|Inborn_genetic_diseases": 2,
    "not_provided|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F": 1,
    "not_provided|XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_specified": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum": 2,
    "ERCC4-related_disorder": 5,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 17,
    "not_provided|Hutchinson-Gilford_syndrome|XFE_progeroid_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|ERCC4-related_disorder": 2,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_specified": 1,
    "not_provided|not_specified|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "ERCC4-related_disorder|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|not_provided": 2,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_specified": 4,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome|Cockayne_syndrome": 1,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|not_provided|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases": 5,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|ERCC4-related_disorder|XFE_progeroid_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|not_provided|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "not_specified|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|not_specified": 1,
    "XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|not_provided|not_specified|Cockayne_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|not_provided|ERCC4-Related_Disorders": 1,
    "Inborn_genetic_diseases|not_specified|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|XFE_progeroid_syndrome|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|Xeroderma_pigmentosum|_type_F/Cockayne_syndrome|not_provided": 1,
    "not_provided|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 1,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|not_specified|not_provided": 1,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|Cockayne_syndrome": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases": 2,
    "not_provided|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome": 6,
    "not_provided|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided": 6,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 4,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 3,
    "Xeroderma_pigmentosum|not_specified|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_provided": 1,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_provided|XFE_progeroid_syndrome": 1,
    "XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 2,
    "not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided": 2,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "not_provided|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_specified": 1,
    "Fanconi_anemia_complementation_group_Q|not_provided|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Cockayne_syndrome|not_specified": 1,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|XFE_progeroid_syndrome|not_provided": 1,
    "ERCC4-related_disorder|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "ERCC4-related_disorder|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Hereditary_cancer-predisposing_syndrome|XFE_progeroid_syndrome|not_specified|not_provided|Xeroderma_pigmentosum": 2,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_provided": 2,
    "Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|XFE_progeroid_syndrome": 2,
    "Xeroderma_pigmentosum|_group_F|ERCC4-related_disorder|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_F|not_specified|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|XFE_progeroid_syndrome|Ovarian_cancer": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided|XFE_progeroid_syndrome|not_specified": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|not_specified|not_provided": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Precursor_B-cell_acute_lymphoblastic_leukemia": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Hutchinson-Gilford_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_F": 1,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|not_provided|Inborn_genetic_diseases": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 3,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|not_provided": 1,
    "ERCC4-related_disorder|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|not_provided": 1,
    "Xeroderma_pigmentosum|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 1,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome": 2,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|ERCC4-related_disorder": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|XFE_progeroid_syndrome": 1,
    "Xeroderma_pigmentosum|not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Hereditary_cancer-predisposing_syndrome|XFE_progeroid_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Spastic_ataxia|Xeroderma_pigmentosum|_type_F/Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum": 1,
    "Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|ERCC4-related_disorder": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome|Cockayne_syndrome|Xeroderma_pigmentosum|_type_F/Cockayne_syndrome|ERCC4-related_disorder|Autosomal_recessive_cerebellar_ataxia": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Ovarian_cancer": 1,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|not_provided|Inborn_genetic_diseases|ERCC4-related_disorder|Cockayne_syndrome": 1,
    "not_specified|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|ERCC4-related_disorder|not_provided|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|not_specified": 1,
    "Xeroderma_pigmentosum|_group_F|ERCC4-related_disorder|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided": 1,
    "XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|not_provided|Fanconi_anemia_complementation_group_Q": 2,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|not_provided|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q": 1,
    "not_provided|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_specified": 1,
    "Inborn_genetic_diseases|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|not_specified": 1,
    "Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|not_specified": 2,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|ERCC4-Related_Disorders|XFE_progeroid_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 1,
    "not_specified|not_provided|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|XFE_progeroid_syndrome|ERCC4-related_disorder": 1,
    "not_specified|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "not_provided|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome|Cockayne_syndrome|Xeroderma_pigmentosum|not_specified": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|XFE_progeroid_syndrome|not_provided": 1,
    "Microcephaly|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Spastic_ataxia": 1,
    "not_specified|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome|not_specified|not_provided|Cockayne_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F": 1,
    "ERCC4-related_disorder|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|not_specified|not_provided|Hutchinson-Gilford_syndrome|Xeroderma_pigmentosum|Carcinoma_of_pancreas|Breast_carcinoma": 1,
    "Ovarian_cancer|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|ERCC4-related_disorder": 1,
    "Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|ERCC4-related_disorder|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|not_specified|Cockayne_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome": 1,
    "Fanconi_anemia_complementation_group_Q|not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|not_provided|XFE_progeroid_syndrome": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Ovarian_cancer|Xeroderma_pigmentosum": 1,
    "not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|Inborn_genetic_diseases|Hutchinson-Gilford_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Cockayne_syndrome|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|XFE_progeroid_syndrome": 1,
    "not_provided|Xeroderma_pigmentosum|_group_F|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|_group_F|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_cancer|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_provided|Xeroderma_pigmentosum|ERCC4-related_disorder": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|not_specified|XFE_progeroid_syndrome|not_provided": 1,
    "Xeroderma_pigmentosum|Inborn_genetic_diseases|not_specified|not_provided|Xeroderma_pigmentosum|_group_F|ERCC4-related_disorder|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "not_specified|Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Xeroderma_pigmentosum|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|Cockayne_syndrome|Fanconi_anemia_complementation_group_Q|Inborn_genetic_diseases|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|XFE_progeroid_syndrome|Fanconi_anemia_complementation_group_Q|Cockayne_syndrome": 1,
    "Xeroderma_pigmentosum|_group_F|not_specified|not_provided": 1,
    "Xeroderma_pigmentosum|_group_F|not_provided": 7,
    "not_provided|Xeroderma_pigmentosum|_group_F": 8,
    "not_specified|Xeroderma_pigmentosum": 1,
    "not_provided|Xeroderma_pigmentosum|_group_F|not_specified": 1,
    "MRTFB-related_disorder": 6,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 610,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided": 10,
    "PARN-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases|not_specified": 1,
    "PARN-related_disorder|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases": 21,
    "not_provided|not_specified|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 7,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_specified|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases": 3,
    "not_specified|PARN-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_specified": 4,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6": 21,
    "not_specified|PARN-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 10,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Familial_Interstitial_Pneumonia|Pulmonary_fibrosis|not_provided": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Pulmonary_fibrosis": 2,
    "PARN-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6|not_specified|not_provided": 1,
    "PARN-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 3,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6": 5,
    "Dyskeratosis_congenita|_autosomal_recessive_6": 8,
    "Pulmonary_fibrosis|PARN-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|PARN-related_disorder": 4,
    "Inborn_genetic_diseases|Pulmonary_fibrosis": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Pulmonary_fibrosis|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Pulmonary_fibrosis|Familial_Interstitial_Pneumonia": 3,
    "PARN-related_disorder": 5,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Dyskeratosis_congenita": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|PARN-related_disorder|not_specified": 1,
    "PARN-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Inborn_genetic_diseases": 1,
    "Telomere_syndrome|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided": 1,
    "not_provided|Familial_Interstitial_Pneumonia|Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_specified": 3,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 9,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|PARN-related_disorder|Inborn_genetic_diseases": 1,
    "Familial_Interstitial_Pneumonia|Pulmonary_fibrosis": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 8,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|PARN-related_disorder|not_specified": 1,
    "Familial_Interstitial_Pneumonia|Pulmonary_fibrosis|not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Pulmonary_fibrosis|Familial_Interstitial_Pneumonia|Dyskeratosis_congenita|_autosomal_recessive_6": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6|not_provided|Pulmonary_fibrosis": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Dyskeratosis_congenita|_autosomal_recessive_6|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|Primary_ciliary_dyskinesia_20": 1,
    "Pulmonary_fibrosis|Familial_Interstitial_Pneumonia|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4|PARN-related_disorder|not_specified|Dyskeratosis_congenita|_autosomal_recessive_6": 1,
    "Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Familial_Interstitial_Pneumonia|Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "Telomere_syndrome|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "not_provided|Pulmonary_fibrosis|Familial_Interstitial_Pneumonia|not_specified|Dyskeratosis_congenita|_autosomal_recessive_6|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_4": 1,
    "PDXDC1-related_disorder": 9,
    "PDXDC1-related_disorder|not_provided": 1,
    "not_provided|PDXDC1-related_disorder": 1,
    "Oromandibular-limb_hypogenesis_spectrum|not_provided": 1,
    "Lissencephaly_4": 49,
    "not_provided|Lissencephaly_4": 9,
    "not_provided|Lissencephaly|_Recessive": 1,
    "not_specified|Lissencephaly_4": 2,
    "not_specified|not_provided|Lissencephaly_4": 3,
    "NDE1-related_microhydranencephaly": 3,
    "NDE1-related_disorder|Inborn_genetic_diseases": 1,
    "NDE1-related_microhydranencephaly|Lissencephaly_4": 1,
    "not_provided|NDE1-related_disorder": 2,
    "Inborn_genetic_diseases|Lissencephaly_4": 2,
    "not_specified|NDE1-related_disorder": 1,
    "Lissencephaly_4|not_specified|not_provided|NDE1-related_microhydranencephaly": 1,
    "Lissencephaly_4|Inborn_genetic_diseases": 2,
    "not_provided|Lissencephaly_4|not_specified|NDE1-related_microhydranencephaly": 1,
    "not_provided|NDE1-related_disorder|Lissencephaly_4": 1,
    "NDE1-related_disorder|not_specified|not_provided|Lissencephaly_4": 1,
    "NDE1-related_disorder|not_provided": 1,
    "not_provided|Lissencephaly_4|NDE1-related_microhydranencephaly": 1,
    "Lissencephaly_4|not_specified": 1,
    "NDE1-related_disorder|not_specified|Lissencephaly_4|NDE1-related_microhydranencephaly|not_provided": 1,
    "NDE1-related_disorder": 1,
    "Lissencephaly_4|not_provided": 2,
    "NDE1-related_disorder|not_specified|not_provided": 1,
    "Lissencephaly_4|NDE1-related_disorder": 1,
    "NDE1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_4": 1,
    "not_provided|Inborn_genetic_diseases|Lissencephaly_4": 1,
    "Lissencephaly_4|not_provided|Inborn_genetic_diseases": 1,
    "Lissencephaly_4|not_provided|not_specified": 1,
    "NDE1-related_microhydranencephaly|Lissencephaly_4|not_provided|Intellectual_disability": 1,
    "not_provided|Lissencephaly_4|Inborn_genetic_diseases": 1,
    "Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 8,
    "Aortic_aneurysm|_familial_thoracic_4": 752,
    "Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 1,
    "Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly|_Recessive|not_provided": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4": 22,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 325,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|not_specified|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder": 4,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Connective_tissue_disorder|Inborn_genetic_diseases|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 58,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4": 29,
    "MYH11-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 8,
    "Visceral_myopathy_2|Aortic_aneurysm|_familial_thoracic_4|Esophageal_and_colonic_dysmotility": 1,
    "Chronic_intestinal_pseudoobstruction|Visceral_myopathy_2|Aortic_aneurysm|_familial_thoracic_4|not_provided|MYH11-related_disorder": 1,
    "MYH11-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 14,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided": 32,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 28,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 280,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided": 23,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_4": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|not_provided|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified": 16,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4": 15,
    "not_provided|not_specified|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder": 4,
    "Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided": 9,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Inborn_genetic_diseases|not_provided|Aortic_aneurysm|_familial_thoracic_4|Isolated_thoracic_aortic_aneurysm|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 32,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified|not_provided": 4,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 8,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 16,
    "Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "MYH11-related_disorder": 4,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "MYH11-related_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_4|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2": 3,
    "Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 34,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified|MYH11-related_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 12,
    "Isolated_thoracic_aortic_aneurysm|Lissencephaly|_Recessive|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Connective_tissue_disorder|Lissencephaly|_Recessive|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "MYH11-related_disorder|Cardiovascular_phenotype|Lissencephaly|_Recessive|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided|Lissencephaly_4": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Cardiovascular_phenotype|Lissencephaly_4|not_specified": 1,
    "Lissencephaly|_Recessive|MYH11-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided": 4,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Inborn_genetic_diseases|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|See_cases": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Cardiovascular_phenotype|Lissencephaly_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 12,
    "MYH11-related_disorder|Connective_tissue_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 6,
    "Lissencephaly_4|not_provided|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|not_specified|Lissencephaly|_Recessive|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 13,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thoracic_aortic_aneurysm_or_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|not_specified|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 10,
    "Lissencephaly|_Recessive|Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive": 1,
    "not_specified|not_provided|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive": 1,
    "not_specified|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly|_Recessive": 1,
    "not_provided|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified|MYH11-related_disorder|not_provided": 1,
    "not_provided|MYH11-related_disorder": 1,
    "Congenital_aneurysm_of_ascending_aorta|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Lissencephaly|_Recessive|not_specified|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Lissencephaly|_Recessive|Familial_aortopathy|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 7,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_4": 16,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive|not_provided": 1,
    "not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified": 10,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Visceral_myopathy_2|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4": 2,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified": 4,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|not_specified": 3,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder": 2,
    "Aortic_aneurysm|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided|not_specified": 3,
    "Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Cardiovascular_phenotype|not_specified": 1,
    "MYH11-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 3,
    "not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Connective_tissue_disorder": 1,
    "Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYH11-related_disorder|Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Connective_tissue_disorder|MYH11-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|MYH11-related_disorder|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_4|See_cases|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Lissencephaly|_Recessive": 1,
    "not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 5,
    "Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly|_Recessive|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Aortic_aneurysm|_familial_thoracic_4": 1,
    "See_cases|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Myopia|Aortic_root_aneurysm|Tricuspid_regurgitation|Mitral_regurgitation|Abnormal_left_ventricle_morphology": 1,
    "not_specified|not_provided|Lissencephaly_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Inborn_genetic_diseases": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NDE1-related_disorder|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Inborn_genetic_diseases|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|NDE1-related_disorder|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4|not_specified": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Inborn_genetic_diseases": 1,
    "Lissencephaly|_Recessive|Cardiovascular_phenotype|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|not_specified|not_provided": 1,
    "Connective_tissue_disorder|MYH11-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|MYH11-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Lissencephaly_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_provided|Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4": 5,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly|_Recessive|Lissencephaly_4": 1,
    "Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4": 8,
    "Aortic_aneurysm|_familial_thoracic_4|Lissencephaly|_Recessive|not_provided|Lissencephaly_4": 2,
    "Lissencephaly_4|not_specified|Aortic_aneurysm|_familial_thoracic_4|not_provided|Lissencephaly|_Recessive": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4|not_specified|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly|_Recessive": 1,
    "MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 1,
    "not_specified|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Lissencephaly_4|not_provided|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified|Lissencephaly|_Recessive": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|Inborn_genetic_diseases": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Lissencephaly|_Recessive|Lissencephaly_4|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Lissencephaly|_Recessive|MYH11-related_disorder|Connective_tissue_disorder|Cardiovascular_phenotype|not_specified|not_provided|Lissencephaly_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4|not_specified|not_provided|Lissencephaly|_Recessive": 1,
    "Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Lissencephaly_4": 1,
    "not_provided|Lissencephaly|_Recessive|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 3,
    "not_provided|Lissencephaly|_Recessive|Lissencephaly_4|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 2,
    "Lissencephaly|_Recessive|Aortic_aneurysm|_familial_thoracic_4|Lissencephaly_4": 3,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2": 1,
    "Connective_tissue_disorder|Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_specified": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Congenital_aneurysm_of_ascending_aorta|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Pulmonic_stenosis|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Cardiovascular_phenotype|not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Lissencephaly|_Recessive": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_aortopathy|Aortic_aneurysm|_familial_thoracic_6|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "MYH11-related_disorder|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_1": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Aortic_dilatation": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Bicuspid_aortic_valve": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "not_provided|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|MYH11-related_disorder|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Isolated_thoracic_aortic_aneurysm|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Isolated_thoracic_aortic_aneurysm|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|See_cases|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4": 2,
    "not_provided|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|Cardiovascular_phenotype|not_specified|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4": 4,
    "MYH11-related_disorder|not_specified|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Connective_tissue_disorder|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "not_specified|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 3,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_provided|not_specified|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "not_provided|not_specified|Marfan_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_provided|not_specified": 1,
    "not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|not_specified|Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_4|Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Congenital_aneurysm_of_ascending_aorta": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2": 2,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_aortopathy|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Ehlers-Danlos_syndrome|_classic_type|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided|See_cases|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Connective_tissue_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder": 2,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|MYH11-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_specified|not_provided": 1,
    "MYH11-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|not_specified|not_provided|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|Aortic_aneurysm|_familial_thoracic_4": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|not_specified|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Megacystis|_microcolon|_hypoperistalsis_syndrome": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Connective_tissue_disorder": 1,
    "MYH11-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "MYH11-related_disorder|Connective_tissue_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "MYH11-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "MYH11-related_disorder|Connective_tissue_disorder|Aortic_aneurysm|_familial_thoracic_4|Congenital_aneurysm_of_ascending_aorta|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Altered_myosin_contractile_function|not_specified|not_provided|Loeys-Dietz_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Joint_hypermobility": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MYH11-related_disorder|Aortic_aneurysm|_familial_thoracic_4": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2": 1,
    "Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Aortic_aneurysm|_familial_thoracic_4|not_provided|not_specified": 1,
    "not_specified|Aortic_aneurysm|_familial_thoracic_4|MYH11-related_disorder": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2": 1,
    "not_provided|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "Aortic_aneurysm|_familial_thoracic_4|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Visceral_myopathy_2|Aortic_aneurysm|_familial_thoracic_4|not_provided": 1,
    "Aortic_aneurysm|_familial_thoracic_4|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Isolated_thoracic_aortic_aneurysm": 1,
    "MYH11-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_specified|not_provided|Visceral_myopathy_2|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_2|Aortic_aneurysm|_familial_thoracic_4|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Cardiovascular_phenotype|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Aortic_aneurysm|_familial_thoracic_4": 1,
    "not_provided|MYH11-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_4": 1,
    "ABCC1-related_disorder": 11,
    "Hearing_loss|_autosomal_dominant_77": 1,
    "not_provided|ABCC1-related_disorder": 1,
    "Atorvastatin_response": 1,
    "not_provided|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 5,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Pseudoxanthoma_elasticum|_forme_fruste": 3,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 185,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 68,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 66,
    "Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 104,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|ABCC6-related_disorder": 3,
    "ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 5,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 24,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 14,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 2,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 37,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|not_provided": 24,
    "Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 6,
    "Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|ABCC6-related_disorder": 2,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 12,
    "not_specified|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 1,
    "ABCC6-related_disorder|not_provided": 17,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|not_specified": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Retinal_dystrophy": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2": 2,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 7,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 2,
    "ABCC6-related_disorder": 13,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 24,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Abnormality_of_the_eye": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 3,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Retinal_dystrophy": 2,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2": 4,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_specified": 2,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|ABCC6-related_disorder|not_provided": 4,
    "ABCC6-related_disorder|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 1,
    "ABCC6-related_disorder|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|not_provided": 4,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Retinal_dystrophy": 1,
    "ABCC6-related_disorder|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "not_provided|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2": 10,
    "Pseudoxanthoma_elasticum|_forme_fruste|not_provided|not_specified|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 2,
    "not_specified|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 3,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Retinal_dystrophy|not_provided": 2,
    "Inborn_genetic_diseases|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|not_provided": 3,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Inborn_genetic_diseases": 2,
    "not_provided|ABCC6-related_disorder": 6,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|ABCC6-related_disorder": 1,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste": 3,
    "Inborn_genetic_diseases|not_provided|ABCC6-related_disorder|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "ABCC6-related_disorder|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 4,
    "ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|See_cases": 1,
    "Pseudoxanthoma_elasticum|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Cutis_laxa|Papule|See_cases": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Abnormality_of_the_eye|not_provided": 1,
    "ABCC6-related_disorder|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|not_specified|not_provided": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Inborn_genetic_diseases": 4,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|not_provided|Inborn_genetic_diseases": 3,
    "Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_specified|not_provided": 6,
    "not_provided|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|not_provided": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|ABCC6-related_disorder": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "not_provided|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "not_specified|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 1,
    "Pseudoxanthoma_elasticum|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 1,
    "not_provided|ABCC6-related_disorder|not_specified|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "Inborn_genetic_diseases|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 2,
    "Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Pseudoxanthoma_elasticum": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|ABCC6-related_disorder|not_provided|Optic_atrophy": 1,
    "not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Inborn_genetic_diseases|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "Inborn_genetic_diseases|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 3,
    "Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|not_specified": 1,
    "not_specified|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 2,
    "Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|See_cases": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|ABCC6-related_disorder|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 2,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste": 4,
    "Pseudoxanthoma_elasticum|_forme_fruste|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Arterial_calcification|_generalized|_of_infancy|_2": 2,
    "Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "ABCC6-related_disorder|Pseudoxanthoma_elasticum|_forme_fruste|not_specified|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "not_provided|ABCC6-related_disorder|Retinal_dystrophy": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|not_provided|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "not_provided|Inborn_genetic_diseases|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|not_provided|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|not_provided|ABCC6-related_disorder": 1,
    "ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_specified|not_provided": 1,
    "not_provided|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 1,
    "Inborn_genetic_diseases|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|not_provided": 1,
    "Retinal_dystrophy|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|not_specified|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste|not_provided": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|not_provided": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "not_provided|ABCC6-related_disorder|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Retinal_dystrophy|not_specified": 1,
    "Inborn_genetic_diseases|See_cases|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste": 2,
    "Pseudoxanthoma_elasticum|_forme_fruste|not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified": 1,
    "Inborn_genetic_diseases|ABCC6-related_disorder|not_provided": 1,
    "ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|Pseudoxanthoma_elasticum|_forme_fruste|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_provided": 3,
    "not_specified|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_provided|Inborn_genetic_diseases": 1,
    "ABCC6-related_disorder|not_specified": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "not_provided|not_specified|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2": 1,
    "ABCC6-related_disorder|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Arterial_calcification|_generalized|_of_infancy|_2|Inborn_genetic_diseases|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste": 1,
    "Inborn_genetic_diseases|not_provided|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "not_provided|Arterial_calcification|_generalized|_of_infancy|_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified": 1,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Pseudoxanthoma_elasticum|_forme_fruste|Arterial_calcification|_generalized|_of_infancy|_2|Inborn_genetic_diseases": 1,
    "Pseudoxanthoma_elasticum|_forme_fruste|Optic_atrophy": 1,
    "not_provided|ABCC6-related_disorder|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Desbuquois_dysplasia_1": 398,
    "Inborn_genetic_diseases|Desbuquois_dysplasia_1": 23,
    "Desbuquois_dysplasia_1|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Desbuquois_dysplasia_1|Desbuquois_dysplasia_2|Inborn_genetic_diseases": 1,
    "Desbuquois_dysplasia_1|Inborn_genetic_diseases": 33,
    "Desbuquois_dysplasia_2|Desbuquois_dysplasia_1|not_provided": 1,
    "Desbuquois_dysplasia_1|not_provided": 39,
    "Desbuquois_dysplasia_1|Desbuquois_dysplasia_2|not_provided": 7,
    "not_provided|Desbuquois_dysplasia_1": 19,
    "Desbuquois_dysplasia_1|XYLT1-related_disorder": 4,
    "not_provided|Desbuquois_dysplasia_1|Desbuquois_dysplasia_2": 3,
    "Desbuquois_dysplasia_1|not_specified|not_provided": 1,
    "Desbuquois_dysplasia_1|XYLT1-related_disorder|not_provided": 2,
    "Desbuquois_dysplasia_2": 11,
    "Desbuquois_dysplasia_1|not_provided|Desbuquois_dysplasia_2": 1,
    "Desbuquois_dysplasia_2|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Desbuquois_dysplasia_1": 1,
    "Desbuquois_dysplasia_1|Inborn_genetic_diseases|not_provided": 3,
    "XYLT1-related_disorder|Desbuquois_dysplasia_1": 3,
    "Desbuquois_dysplasia_2|Desbuquois_dysplasia_1": 1,
    "Desbuquois_dysplasia_1|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Desbuquois_dysplasia_2": 1,
    "XYLT1-related_disorder|Desbuquois_dysplasia_1|not_provided": 1,
    "not_provided|Desbuquois_dysplasia_2": 2,
    "Desbuquois_dysplasia_1|not_provided|Inborn_genetic_diseases": 6,
    "Desbuquois_dysplasia_1|not_provided|XYLT1-related_disorder": 1,
    "XYLT1-related_disorder|Desbuquois_dysplasia_1|Desbuquois_dysplasia_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|not_specified|not_provided": 1,
    "XYLT1-related_disorder|Inborn_genetic_diseases|Desbuquois_dysplasia_1": 2,
    "not_specified|Desbuquois_dysplasia_1|XYLT1-related_disorder|not_provided": 1,
    "Desbuquois_dysplasia_2|not_provided|Desbuquois_dysplasia_1": 1,
    "Desbuquois_dysplasia_1|Desbuquois_dysplasia_2": 1,
    "not_provided|Desbuquois_dysplasia_1|Inborn_genetic_diseases": 2,
    "not_specified|Desbuquois_dysplasia_1|XYLT1-related_disorder|Inborn_genetic_diseases": 1,
    "Desbuquois_dysplasia_2|Autosomal_recessive_inherited_pseudoxanthoma_elasticum": 1,
    "Desbuquois_dysplasia_2|Desbuquois_dysplasia_1|not_provided|Autosomal_recessive_inherited_pseudoxanthoma_elasticum|PSEUDOXANTHOMA_ELASTICUM|_MODIFIER_OF_SEVERITY_OF": 1,
    "XYLT1-related_disorder": 3,
    "XYLT1-related_disorder|not_provided|Desbuquois_dysplasia_1": 1,
    "Diamond-Blackfan_anemia_20": 1,
    "not_provided|Hereditary_spastic_paraplegia_61": 3,
    "Hereditary_spastic_paraplegia_61": 48,
    "Hereditary_spastic_paraplegia_61|ARL6IP1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_61": 2,
    "Hereditary_spastic_paraplegia_61|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_61|not_provided|ARL6IP1-related_disorder": 1,
    "ARL6IP1-related_disorder|not_provided|Hereditary_spastic_paraplegia_61": 1,
    "COQ7-related_disorder": 3,
    "Primary_coenzyme_Q10_deficiency_8": 11,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_9": 4,
    "not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_9|Primary_coenzyme_Q10_deficiency_8": 1,
    "Primary_coenzyme_Q10_deficiency_8|not_provided": 2,
    "not_provided|COQ7-related_disorder": 4,
    "Primary_coenzyme_Q10_deficiency_8|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_9": 1,
    "Primary_coenzyme_Q10_deficiency_8|not_provided|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_9": 1,
    "COQ7-related_disorder|not_specified|not_provided": 1,
    "not_provided|Primary_coenzyme_Q10_deficiency_8": 1,
    "Primary_coenzyme_Q10_deficiency_8|Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_9|not_provided": 1,
    "COQ7-related_disorder|not_provided": 3,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_9|Primary_coenzyme_Q10_deficiency_8|not_provided": 1,
    "Ritscher-Schinzel_syndrome_3": 6,
    "VPS35L-related_disorder|not_provided|Ritscher-Schinzel_syndrome": 1,
    "VPS35L-related_disorder": 2,
    "Ritscher-Schinzel_syndrome_3|not_specified": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_3": 3,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 29,
    "not_specified|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 4,
    "Autosomal_dominant_medullary_cystic_kidney_disease_with_or_without_hyperuricemia|Familial_juvenile_hyperuricemic_nephropathy_type_1": 2,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|Inborn_genetic_diseases": 3,
    "not_provided|Kidney_disorder|UMOD-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1": 3,
    "not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1": 27,
    "Kidney_failure|Familial_juvenile_hyperuricemic_nephropathy_type_1|Inborn_genetic_diseases|not_provided": 1,
    "UMOD-related_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 3,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|Inborn_genetic_diseases|not_provided": 2,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|not_specified|not_provided": 3,
    "not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1|Inborn_genetic_diseases": 2,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|UMOD-related_disorder": 3,
    "not_specified|Kidney_disorder|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "Inborn_genetic_diseases|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 4,
    "UMOD-related_disorder": 14,
    "UMOD-related_disorder|not_provided": 4,
    "not_provided|UMOD-related_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_1": 2,
    "Autosomal_dominant_medullary_cystic_kidney_disease_with_or_without_hyperuricemia|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 4,
    "UMOD-related_disorder|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided|not_specified|Kidney_disorder": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided|UMOD-related_disorder": 1,
    "UMOD-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided|UMOD-related_disorder|Kidney_disorder": 1,
    "Chronic_kidney_disease|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "not_provided|UMOD-related_disorder": 2,
    "UMOD-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1|UMOD-related_disorder": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Familial_juvenile_hyperuricemic_nephropathy_type_1": 6,
    "UMOD-related_disorder|Kidney_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 2,
    "Kidney_disorder|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_specified": 1,
    "Autosomal_dominant_medullary_cystic_kidney_disease_with_or_without_hyperuricemia": 5,
    "not_provided|UMOD-related_disorder|Inborn_genetic_diseases|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "UMOD-related_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|UMOD-related_disorder": 1,
    "Inborn_genetic_diseases|UMOD-related_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "UMOD-related_disorder|Kidney_disorder|not_provided": 1,
    "UMOD-related_disorder|Familial_juvenile_hyperuricemic_nephropathy_type_1": 2,
    "not_specified|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "not_specified|not_provided|Familial_juvenile_hyperuricemic_nephropathy_type_1": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|Kidney_failure": 1,
    "Familial_juvenile_hyperuricemic_nephropathy_type_1|UMOD-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_speech_delay_and_variable_ocular_anomalies": 4,
    "Neurodevelopmental_disorder_with_speech_delay_and_variable_ocular_anomalies|Neurodevelopmental_disorder": 4,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_speech_delay_and_variable_ocular_anomalies|Neurodevelopmental_disorder": 1,
    "not_specified|Spermatogenic_failure_18": 1,
    "Spermatogenic_failure_18|not_specified": 1,
    "ZP2-related_disorder": 9,
    "Oocyte_maturation_defect_6": 8,
    "not_provided|ZP2-related_disorder": 1,
    "ZP2-related_disorder|not_provided": 1,
    "CRYM-related_disorder": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_40": 5,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_40": 2,
    "not_provided|CRYM-related_disorder": 3,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_40": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_40|not_specified": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_40|not_provided|CRYM-related_disorder|not_specified": 1,
    "CRYM-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_40|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_40|not_provided": 1,
    "OTOA-related_disorder|not_provided": 4,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_22|not_provided": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_22": 8,
    "Autosomal_recessive_nonsyndromic_hearing_loss_22": 27,
    "OTOA-related_disorder|not_specified|not_provided": 1,
    "not_specified|OTOA-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_22|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_22|Rare_genetic_deafness": 1,
    "not_provided|OTOA-related_disorder": 2,
    "OTOA-related_disorder|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_22": 2,
    "not_specified|not_provided|OTOA-related_disorder": 1,
    "Usher_syndrome|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_22|OTOA-related_disorder|not_provided|not_specified": 2,
    "OTOA-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_22|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_22": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_22|not_provided": 1,
    "not_specified|not_provided|OTOA-related_disorder|Nonsyndromic_genetic_hearing_loss": 1,
    "not_provided|not_specified|OTOA-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_22|Autosomal_recessive_nonsyndromic_hearing_loss_7": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_22": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_22": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_22|Rare_genetic_deafness|not_provided": 1,
    "OTOA-related_disorder": 5,
    "OTOA-related_disorder|not_provided|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_22|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_22|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_22|OTOA-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_22|Rare_genetic_deafness": 1,
    "not_provided|OTOA-related_disorder|not_specified": 1,
    "not_specified|Hearing_impairment|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_5": 10,
    "UQCRC2-related_disorder": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_5|not_provided": 3,
    "not_provided|UQCRC2-related_disorder": 2,
    "not_provided|not_specified|UQCRC2-related_disorder": 1,
    "not_specified|not_provided|UQCRC2-related_disorder": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_5|not_provided|not_specified": 1,
    "not_provided|UQCRC2-related_disorder|Mitochondrial_complex_III_deficiency_nuclear_type_5": 1,
    "UQCRC2-related_disorder|not_provided|not_specified": 1,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 4,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 9,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Liddle_syndrome_2": 55,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_2": 17,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 3,
    "Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Liddle_syndrome_2": 3,
    "SCNN1G-related_disorder": 3,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Liddle_syndrome_2|Inborn_genetic_diseases": 6,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_2|not_provided|not_specified": 1,
    "not_provided|Liddle_syndrome_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|not_provided": 1,
    "not_specified|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive": 3,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 2,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|not_provided": 1,
    "not_provided|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Liddle_syndrome_2|SCNN1G-related_disorder|not_provided|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_2|not_specified": 1,
    "Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Liddle_syndrome_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|not_provided": 3,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|not_specified": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|Liddle_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Liddle_syndrome_2": 1,
    "Inborn_genetic_diseases|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 3,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|not_provided|not_specified": 1,
    "not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Liddle_syndrome_2": 1,
    "not_provided|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Liddle_syndrome_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Liddle_syndrome_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 2,
    "not_provided|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2": 3,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|SCNN1G-related_disorder": 1,
    "Liddle_syndrome_2|not_provided": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|not_provided": 3,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Liddle_syndrome_2": 14,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_2": 1,
    "Liddle_syndrome_2": 4,
    "Liddle_syndrome_2|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Liddle_syndrome_2|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Liddle_syndrome_2|not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Liddle_syndrome_2|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "not_provided|Liddle_syndrome_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|not_provided": 1,
    "Liddle_syndrome_2|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_2|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|SCNN1G-related_disorder|Liddle_syndrome_2|not_provided|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|SCNN1G-related_disorder|not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 1,
    "Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|SCNN1G-related_disorder|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Liddle_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Liddle_syndrome_2|not_provided|Monosomy_7_myelodysplasia_and_leukemia_syndrome_1|Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "SCNN1G-related_disorder|Pseudohypoaldosteronism|_type_IB3|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Liddle_syndrome_2": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_3|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_2|not_specified|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 2,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|not_provided|SCNN1B-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1": 67,
    "Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 6,
    "not_provided|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 3,
    "Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified|not_provided|SCNN1B-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|SCNN1B-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1": 7,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1|not_provided": 4,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 3,
    "SCNN1B-related_disorder|not_specified|not_provided": 1,
    "SCNN1B-related_disorder|not_provided|not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|SCNN1B-related_disorder|not_provided|Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "SCNN1B-related_disorder|Liddle_syndrome_1|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Inborn_genetic_diseases": 3,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Liddle_syndrome_1": 5,
    "not_provided|Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 1,
    "SCNN1B-related_disorder": 8,
    "Liddle_syndrome_1": 9,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1|not_provided|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|not_provided": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1": 10,
    "SCNN1B-related_disorder|not_specified|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1": 1,
    "not_specified|Inborn_genetic_diseases|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|not_provided": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|not_provided": 4,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|not_specified|not_provided": 2,
    "not_provided|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|not_provided": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1": 7,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|SCNN1B-related_disorder|not_provided": 1,
    "not_provided|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 3,
    "Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|not_provided": 1,
    "not_provided|not_specified|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_specified|not_provided|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "not_provided|Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1": 1,
    "Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Inborn_genetic_diseases|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 1,
    "not_specified|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Liddle_syndrome_1": 2,
    "not_provided|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Inborn_genetic_diseases|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|not_provided|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|SCNN1B-related_disorder|not_provided": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_specified": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young": 4,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|not_provided": 1,
    "not_provided|SCNN1B-related_disorder|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive": 1,
    "SCNN1B-related_disorder|Liddle_syndrome_1|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Opsoclonus-myoclonus_syndrome": 1,
    "Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|not_provided": 2,
    "not_provided|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1": 2,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Low_renin|_low_aldosterone_hypertension": 1,
    "not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Pruritus|_hereditary_localized|SCNN1B-related_disorder|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|not_specified": 1,
    "not_specified|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|not_specified|SCNN1B-related_disorder": 1,
    "not_specified|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|SCNN1B-related_disorder": 1,
    "Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive": 1,
    "Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "SCNN1B-related_disorder|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided|Liddle_syndrome_1": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_specified|not_provided|Liddle_syndrome_1": 1,
    "Bronchiectasis_with_or_without_elevated_sweat_chloride_1|Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|not_provided|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_specified|Liddle_syndrome_1|Pseudohypoaldosteronism|_type_IB2|_autosomal_recessive|Bronchiectasis_with_or_without_elevated_sweat_chloride_1|not_provided": 1,
    "Pseudohypoaldosteronism|_type_IB1|_autosomal_recessive|Liddle_syndrome_1|Bronchiectasis_with_or_without_elevated_sweat_chloride_1": 1,
    "COG7_congenital_disorder_of_glycosylation": 343,
    "not_provided|COG7_congenital_disorder_of_glycosylation": 20,
    "COG7_congenital_disorder_of_glycosylation|not_specified": 10,
    "Inborn_genetic_diseases|COG7_congenital_disorder_of_glycosylation": 20,
    "not_specified|not_provided|COG7_congenital_disorder_of_glycosylation": 2,
    "COG7_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 13,
    "COG7_congenital_disorder_of_glycosylation|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|COG7_congenital_disorder_of_glycosylation": 1,
    "COG7_congenital_disorder_of_glycosylation|COG7-related_disorder": 4,
    "COG7_congenital_disorder_of_glycosylation|COG7-related_disorder|not_provided|not_specified": 1,
    "not_provided|COG7_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 3,
    "COG7_congenital_disorder_of_glycosylation|not_specified|not_provided": 2,
    "COG7-related_disorder|COG7_congenital_disorder_of_glycosylation": 4,
    "not_specified|COG7_congenital_disorder_of_glycosylation": 11,
    "Inborn_genetic_diseases|not_provided|COG7_congenital_disorder_of_glycosylation": 4,
    "COG7-related_disorder|not_specified|COG7_congenital_disorder_of_glycosylation": 1,
    "COG7-related_disorder|not_specified|not_provided|COG7_congenital_disorder_of_glycosylation": 1,
    "not_provided|Inborn_genetic_diseases|COG7_congenital_disorder_of_glycosylation": 3,
    "COG7-related_disorder|COG7_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_specified|COG7_congenital_disorder_of_glycosylation|not_provided": 1,
    "not_specified|COG7-related_disorder|COG7_congenital_disorder_of_glycosylation": 2,
    "COG7-related_disorder|COG7_congenital_disorder_of_glycosylation|not_specified": 2,
    "COG7-related_disorder|not_provided|COG7_congenital_disorder_of_glycosylation": 3,
    "COG7_congenital_disorder_of_glycosylation|COG7-related_disorder|not_specified": 1,
    "not_specified|Congenital_disorder_of_glycosylation|COG7_congenital_disorder_of_glycosylation": 1,
    "COG7-related_disorder": 3,
    "COG7-related_disorder|COG7_congenital_disorder_of_glycosylation|not_provided": 1,
    "COG7_congenital_disorder_of_glycosylation|COG7-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_disorder_of_glycosylation|COG7_congenital_disorder_of_glycosylation": 1,
    "COG7-related_disorder|Inborn_genetic_diseases|not_specified|COG7_congenital_disorder_of_glycosylation": 1,
    "Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 64,
    "not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 29,
    "Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_provided": 8,
    "EARS2-related_disorder": 5,
    "See_cases|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_specified|not_provided": 1,
    "not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_specified": 5,
    "Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_disease|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "not_specified|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_provided": 2,
    "EARS2-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|Mitochondrial_disease": 1,
    "not_provided|EARS2-related_disorder": 2,
    "Mitochondrial_disease|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|not_provided": 1,
    "not_provided|not_specified|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "EARS2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "Motor_delay|Seizure|Abnormal_facial_shape|Abnormal_pinna_morphology|Limb_tremor|Prominent_forehead|Bilateral_tonic-clonic_seizure|Global_developmental_delay|High_palate|See_cases|not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|EARS2-related_disorder|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_specified": 1,
    "EARS2-related_disorder|not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|EARS2-related_disorder": 1,
    "not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "EARS2-related_disorder|not_specified|not_provided|Leukoencephalopathy-thalamus_and_brainstem_anomalies-high_lactate_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 2,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "PALB2-related_cancer_predisposition|PALB2-related_disorder|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "PALB2-related_cancer_predisposition|Familial_cancer_of_breast": 3,
    "Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|PALB2-related_disorder|not_specified": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "PALB2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PALB2-related_cancer_predisposition": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PALB2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast": 1,
    "Chordoma|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Familial_cancer_of_breast": 2,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ovarian_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 2,
    "Breast_and/or_ovarian_cancer|PALB2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast": 7,
    "PALB2-related_cancer_predisposition|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_N|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|not_specified|not_provided|Familial_cancer_of_breast": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Malignant_tumor_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|Familial_cancer_of_breast": 2,
    "not_provided|not_specified|PALB2-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 8,
    "PALB2-related_disorder|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|bilateral_breast_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 16,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 4,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Familial_ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 3,
    "Carcinoma_of_colon|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "PALB2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 3,
    "PALB2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_N": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "PALB2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 6,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 5,
    "Familial_cancer_of_breast|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 2,
    "Fanconi_anemia_complementation_group_N": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|PALB2-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|PALB2-related_disorder": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 1,
    "Gastric_cancer|Familial_cancer_of_breast": 7,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Gastric_cancer|PALB2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|PALB2-related_disorder|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_cancer_predisposition|Anaplastic_ependymoma|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|See_cases": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Carcinoma_of_colon": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_3": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastric_cancer|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Breast_neoplasm|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_specified": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "PALB2-related_disorder": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_provided|not_specified|Familial_cancer_of_breast": 1,
    "not_specified|PALB2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|NICE_approved_PARP_inhibitor_treatment|Inherited_breast_cancer_and_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|PALB2-related_cancer_predisposition|Malignant_tumor_of_breast|PALB2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Carcinoma_of_colon|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Chordoma|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|PALB2-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 7,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 1,
    "PALB2-related_cancer_predisposition|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided|PALB2-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|PALB2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Familial_cancer_of_breast|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "PALB2-related_cancer_predisposition|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|PALB2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided|PALB2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_cancer|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 2,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_pancreas": 3,
    "Carcinoma_of_colon|not_provided|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|not_specified|PALB2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided|Triple-negative_breast_cancer": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_specified|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "not_specified|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PALB2-related_cancer_predisposition|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Gastric_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided": 2,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Diffuse_midline_glioma|_H3_K27-altered|Familial_cancer_of_breast": 1,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Gastric_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|Familial_cancer_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|not_provided|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Chordoma|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Carcinoma_of_colon|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|Familial_cancer_of_breast|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Diffuse_midline_glioma|_H3_K27-altered|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|not_specified|PALB2-related_cancer_predisposition": 1,
    "PALB2-related_disorder|Gastric_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 2,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|PALB2-related_disorder": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "PALB2-related_disorder|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "not_provided|PALB2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Familial_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "PALB2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition|PALB2-related_disorder|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_specified|Endometrial_carcinoma|not_provided|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|not_provided": 2,
    "PALB2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Breast_cancer|_susceptibility_to|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|PALB2-related_disorder|Malignant_tumor_of_breast|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|PALB2-related_disorder": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|B_lymphoblastic_leukemia_lymphoma_with_t(12%3B21)(p13%3Bq22)%3B_TEL-AML1_(ETV6-RUNX1)|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Gastric_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Endometrial_carcinoma|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Gastric_cancer|not_provided": 1,
    "PALB2-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_provided|not_specified": 1,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 5,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|PALB2-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|PALB2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|See_cases|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|Hereditary_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Carcinoma_of_colon|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|PALB2-related_disorder|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|PALB2-related_cancer_predisposition|PALB2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "not_specified|PALB2-related_disorder|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_N|PALB2-related_disorder|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|PALB2-related_disorder": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Gastric_cancer|not_provided": 1,
    "not_provided|Carcinoma_of_colon|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|not_specified|Breast_and/or_ovarian_cancer|Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 2,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Endometrial_carcinoma|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_specified": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Gastric_cancer|Malignant_tumor_of_pancreas|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Papillary_thyroid_carcinoma|not_provided|PALB2-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|PALB2-related_disorder|Familial_cancer_of_breast": 2,
    "Familial_pancreatic_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 2,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|PALB2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided|not_specified": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_cancer|_susceptibility_to|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|PALB2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|PALB2-related_disorder|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|PALB2-related_disorder|not_provided": 1,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 2,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "PALB2-related_disorder|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Malignant_tumor_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|PALB2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "PALB2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_pancreatic_carcinoma|Familial_cancer_of_breast": 1,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Gastric_cancer": 2,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition": 1,
    "not_specified|Fanconi_anemia_complementation_group_N|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Endometrial_carcinoma": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_specified|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|PALB2-related_cancer_predisposition|PALB2-related_disorder": 1,
    "Familial_cancer_of_breast|not_specified|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 2,
    "Malignant_tumor_of_breast|Carcinoma_of_colon|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|PALB2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 83,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PALB2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|PALB2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|PALB2-related_disorder": 1,
    "not_provided|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|PALB2-related_cancer_predisposition|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided|PALB2-related_disorder|Precursor_B-cell_acute_lymphoblastic_leukemia|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Gastric_cancer": 1,
    "Gastric_cancer|Colonic_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided": 2,
    "Familial_cancer_of_breast|Malignant_tumor_of_pancreas|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|not_provided|Fanconi_anemia_complementation_group_N": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_colon|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Chordoma": 1,
    "not_specified|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|PALB2-related_disorder|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Malignant_tumor_of_breast|Breast_carcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|PALB2-related_disorder": 1,
    "PALB2-related_disorder|Familial_ovarian_cancer|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Carcinoma_of_colon": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 34,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|not_specified": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "Familial_cancer_of_breast|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_N": 2,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_cancer": 1,
    "Pilocytic_astrocytoma|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Gastric_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Generalized_hypopigmentation|Basal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PALB2-related_disorder|Familial_cancer_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|not_specified": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|not_specified|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 2,
    "Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 1,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Retinoblastoma|not_specified|Familial_cancer_of_breast|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "not_specified|PALB2-related_disorder|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Breast_cancer|_susceptibility_to": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|PALB2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|Familial_cancer_of_breast|not_specified|not_provided|PALB2-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|PALB2-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Primary_ciliary_dyskinesia_20|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_cancer": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 2,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Neoplasm_of_uterus|Family_history_of_cancer|Malignant_tumor_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|not_provided": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Inherited_breast_cancer_and_ovarian_cancer|Familial_ovarian_cancer|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|not_specified|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Lynch_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Chordoma|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_neoplasm|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|PALB2-related_disorder|not_specified|Familial_cancer_of_breast|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 2,
    "not_specified|Familial_cancer_of_breast|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Carcinoma_of_colon": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition|not_specified|Familial_cancer_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Gastric_cancer|not_provided": 5,
    "Familial_cancer_of_breast|PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|not_provided": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_N|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_N|not_provided|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Neuroendocrine_tumor_of_pancreas": 1,
    "not_specified|Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "PALB2-related_disorder|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_specified|not_provided|Fanconi_anemia": 1,
    "Uterine_corpus_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Malignant_tumor_of_breast|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_provided": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "PALB2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Inherited_prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "PALB2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Breast_neoplasm": 1,
    "Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma": 2,
    "not_specified|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 2,
    "PALB2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Breast_cancer|_susceptibility_to|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "Bile_duct_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast": 2,
    "Malignant_tumor_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast_cancer|_susceptibility_to": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|PALB2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N": 1,
    "Chordoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_specified|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "PALB2-related_disorder|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "PALB2-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_N|PALB2-related_disorder|not_provided|not_specified|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "not_provided|Familial_cancer_of_breast|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Carcinoma_of_colon": 1,
    "PALB2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition|Familial_cancer_of_breast|Colorectal_cancer|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Breast_cancer|_susceptibility_to": 1,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_provided|not_specified": 1,
    "PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|PALB2-related_disorder|not_provided|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_specified": 1,
    "PALB2-related_disorder|Hereditary_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Colorectal_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|not_specified|PALB2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|PALB2-related_disorder": 1,
    "PALB2-related_cancer_predisposition|PALB2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PALB2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|not_provided|Breast_cancer|_susceptibility_to|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_3|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "PALB2-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|not_provided|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Lung_cancer|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Pancreatic_cancer|_susceptibility_to|_3": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|PALB2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|PALB2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Infiltrating_duct_carcinoma_of_breast": 1,
    "not_provided|Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Fanconi_anemia_complementation_group_N|not_specified|not_provided": 1,
    "Pancreatic_cancer|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "PALB2-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_5|PALB2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_N|Familial_cancer_of_breast|not_provided": 1,
    "PALB2-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N|Pancreatic_cancer|_susceptibility_to|_3|Esophageal_atresia/tracheoesophageal_fistula|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_5|Fanconi_anemia_complementation_group_N": 1,
    "PALB2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_N": 1,
    "Fanconi_anemia_complementation_group_N|Hereditary_cancer-predisposing_syndrome": 1,
    "PRKCB-related_disorder": 7,
    "PRKCB-related_disorder|not_provided": 2,
    "PRKCB-related_disorder|not_specified": 1,
    "RBBP6-related_disorder|not_specified": 2,
    "RBBP6-related_disorder": 2,
    "Epilepsy|_familial_adult_myoclonic|_6": 2,
    "Epilepsy|_familial_adult_myoclonic|_6|not_provided": 5,
    "not_provided|Epilepsy|_familial_adult_myoclonic|_6": 1,
    "not_specified|Epilepsy|_familial_adult_myoclonic|_6": 1,
    "Microcephaly_6_with_or_without_short_stature": 2,
    "IL4R-related_disorder|not_provided": 2,
    "IgE_responsiveness|_atopic": 1,
    "IL4R-related_disorder|RECLASSIFIED_-_MYOC_POLYMORPHISM": 1,
    "IL4R-related_disorder": 13,
    "IgE_responsiveness|_atopic|Susceptibility_to_HIV_infection|IL4R-related_disorder|not_provided": 1,
    "Susceptibility_to_HIV_infection|IgE_responsiveness|_atopic|not_provided": 1,
    "Increased_circulating_IgE_concentration|not_provided": 1,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 280,
    "IgE_responsiveness|_atopic|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|not_provided": 1,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|Inborn_genetic_diseases": 15,
    "Inborn_genetic_diseases|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 18,
    "not_provided|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 5,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|not_provided": 8,
    "IL21R-related_disorder|not_specified|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 2,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|IL21R-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 1,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|Autoimmune_enteropathy_and_endocrinopathy_-_susceptibility_to_chronic_infections_syndrome": 1,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|IgE_responsiveness|_atopic|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 1,
    "Inborn_genetic_diseases|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|IgE_responsiveness|_atopic|not_specified|not_provided": 1,
    "IgE_responsiveness|_atopic|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|IgE_responsiveness|_atopic|not_provided": 1,
    "not_specified|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 1,
    "IL21R-related_disorder": 2,
    "IL21R-related_disorder|Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome": 2,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|IL21R-related_disorder|not_provided": 1,
    "Cryptosporidiosis-chronic_cholangitis-liver_disease_syndrome|IgE_responsiveness|_atopic": 1,
    "Joubert_syndrome_26|not_provided": 2,
    "not_provided|Joubert_syndrome_26|See_cases": 1,
    "not_provided|Joubert_syndrome_26": 3,
    "KATNIP-related_disorder|not_provided": 17,
    "Joubert_syndrome_26": 15,
    "KATNIP-related_disorder|not_specified": 1,
    "KATNIP-related_disorder": 9,
    "Ciliopathy|not_specified|not_provided": 1,
    "not_specified|not_provided|KATNIP-related_disorder": 3,
    "not_provided|KATNIP-related_disorder": 11,
    "KATNIP-related_disorder|not_specified|not_provided": 2,
    "not_specified|KATNIP-related_disorder|not_provided": 2,
    "not_specified|KATNIP-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_26": 1,
    "not_specified|Joubert_syndrome_26": 1,
    "not_provided|not_specified|Joubert_syndrome_26": 1,
    "not_provided|KATNIP-related_disorder|not_specified": 1,
    "not_provided|KATNIP-related_disorder|Joubert_syndrome_26": 1,
    "not_provided|Joubert_syndrome_26|Joubert_syndrome_1": 1,
    "not_provided|not_specified|KATNIP-related_disorder": 1,
    "KATNIP-related_disorder|not_provided|not_specified": 1,
    "KATNIP-related_disorder|Joubert_syndrome_26|not_provided": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_3": 8,
    "Neuronal_ceroid_lipofuscinosis_3": 76,
    "not_provided|Neuronal_ceroid_lipofuscinosis_3": 3,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided|Neuronal_ceroid_lipofuscinosis_3": 4,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Inborn_genetic_diseases": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 11,
    "Syndromic_inherited_retinal_disease": 1,
    "Neuronal_ceroid_lipofuscinosis|Retinitis_pigmentosa": 2,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|not_provided": 2,
    "early_onset_and_severe_retinal_dystrophy|not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 31,
    "CLN3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 4,
    "Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis|Retinitis_pigmentosa|not_provided|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|not_specified": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis_3|not_specified|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Neuronal_ceroid_lipofuscinosis_3|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 1,
    "CLN3-related_disorder|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 3,
    "Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 26,
    "not_provided|Neuronal_ceroid_lipofuscinosis_3|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases": 1,
    "Juvenile_neuronal_ceroid_lipofuscinosis": 23,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 4,
    "Juvenile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis": 6,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3": 2,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 1,
    "CLN3-related_disorder|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Neuronal_ceroid_lipofuscinosis_3|not_provided|Neuronal_ceroid_lipofuscinosis": 4,
    "Cone-rod_dystrophy|Neuronal_ceroid_lipofuscinosis_3|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|not_provided": 2,
    "early_onset_and_severe_retinal_dystrophy|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Ceroid_lipofuscinosis|_neuronal|_3|_protracted": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis|not_provided": 4,
    "Neuronal_ceroid_lipofuscinosis|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis_3|not_specified|Retinitis_pigmentosa|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Retinitis_pigmentosa|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 2,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_3": 2,
    "not_specified|not_provided|Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_3|_protracted|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Juvenile_neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|not_provided|not_specified": 1,
    "Juvenile_neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Retinal_dystrophy": 1,
    "Neuronal_ceroid_lipofuscinosis_3|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_3": 4,
    "Neuronal_ceroid_lipofuscinosis|Juvenile_neuronal_ceroid_lipofuscinosis": 2,
    "not_provided|Neuronal_ceroid_lipofuscinosis_3|Retinitis_pigmentosa": 1,
    "Neuronal_ceroid_lipofuscinosis_3|not_provided|Retinitis_pigmentosa": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_specified|Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Retinitis_pigmentosa": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Ceroid_lipofuscinosis|_neuronal|_3|_protracted|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_provided|CLN3-related_disorder|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Retinal_dystrophy|not_provided|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Juvenile_neuronal_ceroid_lipofuscinosis": 1,
    "Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Neuronal_ceroid_lipofuscinosis|Retinitis_pigmentosa|Retinal_dystrophy|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Ceroid_lipofuscinosis|_neuronal|_3|_protracted": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3": 3,
    "CLN3-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 1,
    "Intellectual_disability|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_3|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "CLN3-related_disorder|Inborn_genetic_diseases|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Retinitis_pigmentosa|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis_3|not_specified|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis_3|not_provided": 1,
    "Retinal_dystrophy|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|Neuronal_ceroid_lipofuscinosis": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|Progressive_myoclonic_epilepsy_type_3": 1,
    "not_provided|Neuronal_ceroid_lipofuscinosis|CLN3-related_disorder|Neuronal_ceroid_lipofuscinosis_3|not_specified|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_3|CLN3-related_disorder|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Neuronal_ceroid_lipofuscinosis_3|not_specified|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3": 1,
    "not_specified|Neuronal_ceroid_lipofuscinosis_3|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_3|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_3|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_ceroid_lipofuscinosis_3|CLN3-related_disorder": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_3|not_provided": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Dominant/Recessive|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_4|not_provided": 9,
    "Combined_oxidative_phosphorylation_defect_type_4": 33,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_4": 4,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_4": 1,
    "not_provided|TUFM-related_disorder|Combined_oxidative_phosphorylation_defect_type_4": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_4": 4,
    "not_provided|TUFM-related_disorder": 2,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_4": 2,
    "TUFM-related_disorder|not_provided": 2,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_4": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_4|TUFM-related_disorder": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_4|not_provided": 1,
    "Combined_oxidative_phosphorylation_defect_type_4|not_provided|not_specified": 1,
    "TUFM-related_disorder|not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_4": 1,
    "TUFM-related_disorder|Combined_oxidative_phosphorylation_defect_type_4|not_provided": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_4": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_4|not_provided": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_4": 1,
    "TUFM-related_disorder|not_provided|Combined_oxidative_phosphorylation_defect_type_4": 1,
    "SH2B1-related_disorder": 192,
    "SH2B1-related_disorder|not_provided": 27,
    "not_specified|SH2B1-related_disorder": 12,
    "not_provided|SH2B1-related_disorder": 22,
    "SH2B1-related_disorder|not_provided|not_specified": 3,
    "SH2B1-related_disorder|not_specified": 6,
    "not_provided|SH2B1-related_disorder|not_specified": 1,
    "not_specified|SH2B1-related_disorder|not_provided": 2,
    "not_provided|not_specified|SH2B1-related_disorder": 3,
    "SH2B1-associated_obesity|SH2B1-associated_disorder": 1,
    "not_provided|Severe_early-onset_obesity-insulin_resistance_syndrome_due_to_SH2B1_deficiency": 1,
    "SH2B1-related_disorder|not_specified|not_provided": 2,
    "SH2B1-related_disorder|not_provided|Premature_ovarian_failure|Distal_16p11.2_microdeletion_syndrome": 1,
    "not_specified|not_provided|SH2B1-related_disorder": 1,
    "Brody_myopathy|not_provided|not_specified": 3,
    "Brody_myopathy": 603,
    "not_specified|Brody_myopathy": 7,
    "Brody_myopathy|not_provided": 28,
    "ATP2A1-related_disorder|not_provided|Brody_myopathy": 4,
    "not_provided|Inborn_genetic_diseases|Brody_myopathy": 6,
    "Brody_myopathy|ATP2A1-related_disorder": 3,
    "ATP2A1-related_disorder|Brody_myopathy|not_provided": 3,
    "Inborn_genetic_diseases|Brody_myopathy": 12,
    "not_provided|Brody_myopathy": 32,
    "Inborn_genetic_diseases|Brody_myopathy|not_provided": 2,
    "Brody_myopathy|Inborn_genetic_diseases": 16,
    "ATP2A1-related_disorder|Brody_myopathy": 4,
    "ATP2A1-related_disorder": 2,
    "not_provided|Brody_myopathy|Inborn_genetic_diseases": 4,
    "Brody_myopathy|not_specified": 8,
    "not_provided|Brody_myopathy|Inborn_genetic_diseases|not_specified": 1,
    "ATP2A1-related_disorder|not_specified|not_provided|Brody_myopathy": 2,
    "not_provided|not_specified|Brody_myopathy": 2,
    "ATP2A1-related_disorder|Brody_myopathy|Inborn_genetic_diseases": 1,
    "not_specified|Brody_myopathy|not_provided": 1,
    "not_specified|ATP2A1-related_disorder|not_provided|Brody_myopathy": 1,
    "Brody_myopathy|not_specified|not_provided": 1,
    "not_provided|Brody_myopathy|ATP2A1-related_disorder": 1,
    "See_cases|not_provided|not_specified|Brody_myopathy": 1,
    "Brody_myopathy|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Brody_myopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Brody_myopathy": 1,
    "ATP2A1-related_disorder|Brody_myopathy|not_provided|not_specified": 1,
    "not_provided|Brody_myopathy|not_specified": 3,
    "ATP2A1-related_disorder|Brody_myopathy|not_specified": 1,
    "not_specified|not_provided|Brody_myopathy": 2,
    "Brody_myopathy|not_provided|Inborn_genetic_diseases": 1,
    "Brody_myopathy|ATP2A1-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|ATP2A1-related_disorder|not_provided|Brody_myopathy|See_cases": 1,
    "not_specified|Brody_myopathy|ATP2A1-related_disorder": 1,
    "Immunodeficiency|_common_variable|_3": 24,
    "Immunodeficiency|_common_variable|_3|not_provided": 17,
    "Immunodeficiency|_common_variable|_3|Inborn_genetic_diseases": 1,
    "not_provided|Immunodeficiency|_common_variable|_3|CD19-related_disorder": 1,
    "not_provided|Immunodeficiency|_common_variable|_3": 7,
    "not_provided|CD19-related_disorder|Immunodeficiency|_common_variable|_3": 1,
    "Immunodeficiency|_common_variable|_3|not_specified|not_provided": 3,
    "Immunodeficiency|_common_variable|_3|Inborn_genetic_diseases|not_provided": 2,
    "CD19-related_disorder": 3,
    "CD19-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency|_common_variable|_3": 1,
    "not_provided|CD19-related_disorder": 3,
    "Immunodeficiency|_common_variable|_2|Immunodeficiency|_common_variable|_3|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_3": 1,
    "Immunodeficiency|_common_variable|_3|CD19-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Common_Variable_Immune_Deficiency|_Recessive": 2,
    "Common_Variable_Immune_Deficiency|_Recessive": 2,
    "Severe_combined_immunodeficiency_due_to_LAT_deficiency": 3,
    "not_provided|LAT-related_disorder": 3,
    "LAT-related_disorder": 1,
    "not_specified|not_provided|Severe_combined_immunodeficiency_due_to_LAT_deficiency": 1,
    "Severe_combined_immunodeficiency_due_to_LAT_deficiency|not_provided": 3,
    "not_provided|Severe_combined_immunodeficiency_due_to_LAT_deficiency": 1,
    "SPN-related_disorder": 6,
    "not_provided|SPN-related_disorder": 2,
    "SPN-related_disorder|not_provided": 1,
    "Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations|not_provided": 4,
    "not_specified|Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations": 1,
    "Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations": 13,
    "KIF22-related_disorder": 4,
    "not_provided|Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations": 6,
    "Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations|See_cases": 1,
    "not_provided|KIF22-related_disorder": 3,
    "not_specified|KIF22-related_disorder|not_provided": 1,
    "KIF22-related_disorder|not_provided": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations|Inborn_genetic_diseases": 1,
    "not_provided|KIF22-related_disorder|not_specified": 1,
    "Spondyloepimetaphyseal_dysplasia_with_multiple_dislocations|not_specified": 2,
    "KIF22-related_disorder|not_specified|not_provided": 1,
    "Seizures|_benign_familial_infantile|_2": 12,
    "Episodic_kinesigenic_dyskinesia|not_provided": 34,
    "Episodic_kinesigenic_dyskinesia_1|Episodic_kinesigenic_dyskinesia": 3,
    "Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia": 12,
    "Episodic_kinesigenic_dyskinesia_1": 10,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases": 20,
    "not_specified|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases": 1,
    "not_specified|Episodic_kinesigenic_dyskinesia": 7,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|PRRT2-related_disorder|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|not_provided": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|Inborn_genetic_diseases": 4,
    "Episodic_kinesigenic_dyskinesia|not_specified": 8,
    "Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis": 3,
    "Episodic_kinesigenic_dyskinesia|Seizure|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia|PRRT2-related_disorder": 1,
    "not_provided|Episodic_kinesigenic_dyskinesia": 28,
    "PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia": 3,
    "PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases": 1,
    "Episodic_kinesigenic_dyskinesia|Complex_febrile_seizure": 1,
    "PRRT2-related_disorder": 3,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|not_specified|not_provided": 3,
    "Seizures|_benign_familial_infantile|_2|not_provided": 1,
    "Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis": 1,
    "Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia_1": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|Episodic_kinesigenic_dyskinesia_1": 3,
    "not_provided|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases": 1,
    "Episodic_kinesigenic_dyskinesia|not_specified|Inborn_genetic_diseases": 1,
    "Infantile_convulsions_and_choreoathetosis": 6,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|not_specified|not_provided|Episodic_kinesigenic_dyskinesia_1": 1,
    "not_provided|Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia": 2,
    "not_provided|PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases": 1,
    "not_specified|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases": 1,
    "Episodic_kinesigenic_dyskinesia|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|Seizures|_benign_familial_infantile|_2|not_provided": 1,
    "Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia|Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis|not_specified|not_provided": 1,
    "PRRT2-related_disorder|Inborn_genetic_diseases": 1,
    "Infantile_convulsions_and_choreoathetosis|Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia_1": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|Infantile_convulsions_and_choreoathetosis": 1,
    "Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia|not_specified": 1,
    "not_provided|Seizures|_benign_familial_infantile|_2": 2,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|not_specified": 1,
    "Episodic_kinesigenic_dyskinesia|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|not_provided": 1,
    "not_provided|Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2": 1,
    "Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia|not_provided": 1,
    "Episodic_kinesigenic_dyskinesia_1|PRRT2-related_disorder": 1,
    "PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis|not_provided": 1,
    "Self-limited_familial_infantile_epilepsy|PRRT2-Associated_Paroxysmal_Movement_Disorders|Inborn_genetic_diseases|PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis|not_provided|Paroxysmal_nonkinesigenic_dyskinesia_1|Neurodevelopmental_delay|Seizure|PRRT2_insufficiency|Convulsions|See_cases": 1,
    "PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|PRRT2-associated_paroxysmal_movement_disorder|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|not_provided": 1,
    "PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|not_provided|Inborn_genetic_diseases": 1,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|PRRT2-related_disorder|Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia_1|not_specified|not_provided": 1,
    "Episodic_kinesigenic_dyskinesia|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|not_specified|PRRT2-related_disorder|Inborn_genetic_diseases|Infantile_convulsions_and_choreoathetosis|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia": 1,
    "Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Infantile_convulsions_and_choreoathetosis|not_specified|not_provided|Seizure": 1,
    "not_provided|Infantile_convulsions_and_choreoathetosis|PRRT2-associated_paroxysmal_movement_disorder|Episodic_kinesigenic_dyskinesia|Seizures|_benign_familial_infantile|_2": 1,
    "Global_developmental_delay|Hyperactivity|Seizure|Intellectual_disability|_profound|Infantile_convulsions_and_choreoathetosis": 1,
    "Infantile_convulsions_and_choreoathetosis|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|not_provided|Episodic_kinesigenic_dyskinesia": 1,
    "See_cases|Episodic_kinesigenic_dyskinesia": 1,
    "PRRT2-Associated_Paroxysmal_Movement_Disorders|Episodic_kinesigenic_dyskinesia|not_provided": 1,
    "not_provided|Episodic_kinesigenic_dyskinesia|not_specified": 1,
    "Episodic_kinesigenic_dyskinesia|Infantile_convulsions_and_choreoathetosis|Seizures|_benign_familial_infantile|_2|not_specified|Episodic_kinesigenic_dyskinesia_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Episodic_kinesigenic_dyskinesia": 2,
    "Episodic_kinesigenic_dyskinesia|Seizure": 1,
    "Inborn_genetic_diseases|Episodic_kinesigenic_dyskinesia|Infantile_convulsions_and_choreoathetosis|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|not_specified|not_provided": 1,
    "Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia": 3,
    "Episodic_kinesigenic_dyskinesia_1|Episodic_kinesigenic_dyskinesia|not_specified": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|Inborn_genetic_diseases|not_specified|PRRT2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Episodic_kinesigenic_dyskinesia|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2": 1,
    "Episodic_kinesigenic_dyskinesia|not_specified|not_provided": 1,
    "Seizures|_benign_familial_infantile|_2|not_provided|Episodic_kinesigenic_dyskinesia": 1,
    "Episodic_kinesigenic_dyskinesia_1|Episodic_kinesigenic_dyskinesia|Seizures|_benign_familial_infantile|_2|Infantile_convulsions_and_choreoathetosis|not_provided": 1,
    "not_provided|Episodic_kinesigenic_dyskinesia|Seizures|_benign_familial_infantile|_2": 1,
    "Episodic_kinesigenic_dyskinesia|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1": 1,
    "Episodic_kinesigenic_dyskinesia|Inborn_genetic_diseases|not_provided": 1,
    "PRRT2-related_disorder|Episodic_kinesigenic_dyskinesia|Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2|not_provided": 1,
    "not_provided|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia_1|Episodic_kinesigenic_dyskinesia|Infantile_convulsions_and_choreoathetosis": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|Seizure": 1,
    "Episodic_kinesigenic_dyskinesia_and_familial_infantile_convulsions_with_paroxysmal_choreoathetosis|Episodic_kinesigenic_dyskinesia": 1,
    "Episodic_kinesigenic_dyskinesia_1|Episodic_kinesigenic_dyskinesia|not_provided": 1,
    "Inborn_genetic_diseases|Infantile_convulsions_and_choreoathetosis|Episodic_kinesigenic_dyskinesia_1|Seizures|_benign_familial_infantile|_2|Episodic_kinesigenic_dyskinesia": 1,
    "Episodic_kinesigenic_dyskinesia|not_provided|PRRT2-related_disorder": 1,
    "Episodic_kinesigenic_dyskinesia|PRRT2-related_disorder": 1,
    "Episodic_kinesigenic_dyskinesia_1|not_specified|Episodic_kinesigenic_dyskinesia": 1,
    "PRRT2-related_disorder|not_provided": 1,
    "PRRT2-related_disorder|not_specified|not_provided": 1,
    "lethal_neurodevelopmental_disorder|Neurodevelopmental_disorder|not_provided": 1,
    "KCTD13-related_disorder": 3,
    "not_specified|KCTD13-related_disorder": 1,
    "not_provided|TAOK2-related_disorder": 8,
    "TAOK2-related_disorder": 13,
    "TAOK2-related_disorder|not_provided": 11,
    "not_provided|TAOK2-associated_neurodevelopmental_disorder": 1,
    "TAOK2-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|TAOK2-related_disorder": 1,
    "TAOK2-associated_neurodevelopmental_disorder": 1,
    "Cone-rod_dystrophy_22": 3,
    "ALDOA-related_disorder": 2,
    "HNSHA_due_to_aldolase_A_deficiency|not_provided": 9,
    "HNSHA_due_to_aldolase_A_deficiency": 201,
    "HNSHA_due_to_aldolase_A_deficiency|Inborn_genetic_diseases": 5,
    "not_provided|HNSHA_due_to_aldolase_A_deficiency|ALDOA-related_disorder": 2,
    "ALDOA-related_disorder|HNSHA_due_to_aldolase_A_deficiency": 2,
    "Inborn_genetic_diseases|HNSHA_due_to_aldolase_A_deficiency": 4,
    "not_provided|HNSHA_due_to_aldolase_A_deficiency": 6,
    "ALDOA-related_disorder|not_provided|HNSHA_due_to_aldolase_A_deficiency": 2,
    "HNSHA_due_to_aldolase_A_deficiency|not_specified": 8,
    "not_specified|HNSHA_due_to_aldolase_A_deficiency": 5,
    "not_specified|not_provided|HNSHA_due_to_aldolase_A_deficiency": 1,
    "HNSHA_due_to_aldolase_A_deficiency|ALDOA-related_disorder": 3,
    "HNSHA_due_to_aldolase_A_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|HNSHA_due_to_aldolase_A_deficiency|not_specified": 1,
    "not_provided|ALDOA-related_disorder|HNSHA_due_to_aldolase_A_deficiency": 1,
    "HNSHA_due_to_aldolase_A_deficiency|ALDOA-related_disorder|not_specified": 1,
    "HNSHA_due_to_aldolase_A_deficiency|not_specified|not_provided": 2,
    "Spondylocostal_dysostosis_5|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_5": 19,
    "Scoliosis": 8,
    "TBX6-related_disorder|not_provided": 4,
    "not_provided|Scoliosis": 2,
    "TBX6-related_disorder": 3,
    "not_provided|Spondylocostal_dysostosis_5": 3,
    "Spondylocostal_dysostosis_5|not_provided": 2,
    "not_provided|Spondylocostal_dysostosis_5|not_specified": 1,
    "not_provided|TBX6-related_disorder": 2,
    "Neurodevelopmental_abnormality|not_provided|Spondylocostal_dysostosis_5|TBX6-related_disorder": 1,
    "not_provided|Spondylocostal_dysostosis_5|TBX6-related_disorder": 1,
    "Scoliosis|not_provided|Spondylocostal_dysostosis_5": 1,
    "not_provided|Scoliosis|TBX6-related_disorder|Spondylocostal_dysostosis_5": 1,
    "not_specified|Spondylocostal_dysostosis_5": 1,
    "YPEL3-related_condition": 1,
    "MAPK3-related_disorder": 4,
    "MAPK3-related_disorder|not_provided": 1,
    "not_provided|MAPK3-related_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 262,
    "Sinoatrial_node_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|CORO1A-related_disorder": 2,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|Inborn_genetic_diseases": 2,
    "Autism_spectrum_disorder|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 1,
    "not_specified|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_provided": 1,
    "CORO1A-related_disorder|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_provided": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 3,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 5,
    "CORO1A-related_disorder|not_specified|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 1,
    "CORO1A-related_disorder|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 3,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_provided": 4,
    "not_specified|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_provided|CORO1A-related_disorder": 1,
    "not_provided|not_specified|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 1,
    "not_provided|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_specified": 3,
    "not_specified|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 1,
    "not_provided|CORO1A-related_disorder|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency": 1,
    "not_provided|CORO1A-related_disorder|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency_due_to_CORO1A_deficiency|not_specified": 1,
    "Arthrogryposis|_distal|_type_1C": 3,
    "Distal_arthrogryposis|Arthrogryposis|_distal|_type_1C": 3,
    "Arthrogryposis|_distal|_type_1C|Distal_arthrogryposis": 1,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 14,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 182,
    "Inborn_genetic_diseases|not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 3,
    "not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 30,
    "not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 39,
    "Floating-Harbor_syndrome": 43,
    "Inborn_genetic_diseases|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 10,
    "not_provided|Inborn_genetic_diseases|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 6,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_specified": 2,
    "not_provided|SRCAP-related_disorder": 4,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided": 43,
    "not_specified|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided": 2,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided": 36,
    "Floating-Harbor_syndrome|not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_specified": 1,
    "SRCAP-related_disorder": 24,
    "not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|SRCAP-related_disorder": 2,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided|not_specified": 2,
    "not_provided|Floating-Harbor_syndrome": 2,
    "Floating-Harbor_syndrome|not_provided": 3,
    "SRCAP-related_disorder|not_provided": 16,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided|not_specified": 2,
    "Neurodevelopmental_disorder|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 3,
    "Inborn_genetic_diseases|not_specified|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided": 1,
    "SRCAP-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|Inborn_genetic_diseases": 9,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 2,
    "Inborn_genetic_diseases|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided": 3,
    "not_specified|not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 4,
    "Inborn_genetic_diseases|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided": 5,
    "not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Inborn_genetic_diseases": 5,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided|SRCAP-related_disorder": 2,
    "Inborn_genetic_diseases|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 2,
    "not_provided|SRCAP-related_disorder|Inborn_genetic_diseases|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 3,
    "not_specified|Floating-Harbor_syndrome": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|SRCAP-related_disorder|not_provided": 2,
    "not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Floating-Harbor_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SRCAP-related_disorder": 3,
    "SRCAP-related_disorder|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided": 3,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_specified|not_provided": 2,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 1,
    "not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 2,
    "not_provided|not_specified|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 1,
    "SRCAP-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 1,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|Neurodevelopmental_disorder": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Inborn_genetic_diseases": 2,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Intellectual_disability|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided": 1,
    "Floating-Harbor_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|SRCAP-related_disorder|not_provided": 2,
    "SRCAP-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|Inborn_genetic_diseases": 1,
    "SRCAP-related_disorder|not_provided|Floating-Harbor_syndrome": 1,
    "Neurodevelopmental_disorder|not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|SRCAP-related_disorder": 1,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided": 2,
    "not_specified|not_provided|Floating-Harbor_syndrome": 1,
    "not_specified|not_provided|SRCAP-related_disorder": 1,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|SRCAP-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|SRCAP-related_disorder|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 1,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|SRCAP-related_disorder": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|SRCAP-related_disorder|not_provided": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided|46|XY_disorder_of_sex_development": 1,
    "Inborn_genetic_diseases|not_provided|Floating-Harbor_syndrome": 2,
    "SRCAP-related_disorder|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Inborn_genetic_diseases|Developmental_delay|not_provided|Floating-Harbor_syndrome|See_cases|Neurodevelopmental_delay": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Inborn_genetic_diseases|not_provided": 7,
    "not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_specified": 2,
    "Inborn_genetic_diseases|Floating-Harbor_syndrome": 1,
    "Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|SRCAP-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Floating-Harbor_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|SRCAP-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided": 1,
    "SRCAP-related_disorder|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "SRCAP-related_disorder|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome|not_provided": 1,
    "not_provided|SRCAP-related_disorder|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 1,
    "SRCAP-related_disorder|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|SRCAP-related_disorder|not_specified|not_provided": 1,
    "SRCAP-related_disorder|not_provided|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|Floating-Harbor_syndrome": 1,
    "not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_specified|Inborn_genetic_diseases": 1,
    "Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities|not_provided|Inborn_genetic_diseases": 1,
    "SRCAP-related_disorder|Inborn_genetic_diseases": 1,
    "SRCAP-related_disorder|not_provided|Floating-Harbor_syndrome|Developmental_delay|_hypotonia|_musculoskeletal_defects|_and_behavioral_abnormalities": 1,
    "Glycogen_storage_disease_IXc": 277,
    "Glycogen_storage_disease_IXc|not_provided": 4,
    "Glycogen_phosphorylase_kinase_deficiency": 24,
    "Glycogen_storage_disease_IXc|not_specified": 4,
    "Glycogen_phosphorylase_kinase_deficiency|Inborn_genetic_diseases|Glycogen_storage_disease_IXc": 1,
    "Glycogen_storage_disease_IXc|PHKG2-related_disorder": 2,
    "not_specified|Glycogen_storage_disease_IXc": 6,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXc": 3,
    "not_provided|Glycogen_storage_disease_IXc": 5,
    "not_specified|not_provided|Glycogen_storage_disease_IXc": 1,
    "Glycogen_storage_disease_IXc|Inborn_genetic_diseases": 7,
    "Glycogen_storage_disease_IXc|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Glycogen_storage_disease_IXc": 2,
    "not_provided|Glycogen_storage_disease_IXc|not_specified": 1,
    "PHKG2-related_disorder|not_provided|not_specified|Glycogen_storage_disease_IXc": 1,
    "PHKG2-related_disorder|Glycogen_storage_disease_IXc": 2,
    "PHKG2-related_disorder|not_provided|Glycogen_storage_disease_IXc": 1,
    "Glycogen_storage_disease_type_IXc|Glycogen_storage_disease_IXc": 1,
    "Glycogen_storage_disease_IXc|Glycogen_phosphorylase_kinase_deficiency": 3,
    "Glycogen_storage_disease_IXc|Glycogen_storage_disease_type_IXc": 1,
    "PHKG2-related_disorder|Glycogen_storage_disease_IXc|Glycogen_phosphorylase_kinase_deficiency": 1,
    "not_specified|not_provided|Mauriac_syndrome|Glycogen_storage_disease_IXc": 1,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_IXc": 1,
    "not_provided|Glycogen_storage_disease_IXc|PHKG2-related_disorder|not_specified": 1,
    "not_specified|Glycogen_storage_disease_IXc|not_provided": 1,
    "Glycogen_phosphorylase_kinase_deficiency|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|not_specified|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_Cardiomyopathy|_Dominant|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 5,
    "Primary_dilated_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Dilated_Cardiomyopathy|_Dominant|Cardiomyopathy|not_provided|not_specified": 1,
    "CTF1-related_disorder|not_specified|Cardiomyopathy": 1,
    "Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 41,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay": 15,
    "Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|Epilepsy|_early-onset|_with_or_without_developmental_delay": 9,
    "SETD1A-related_disorder": 39,
    "not_provided|Schizophrenia": 2,
    "Inborn_genetic_diseases|SETD1A-related_disorder": 4,
    "SETD1A-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 5,
    "Inborn_genetic_diseases|Epilepsy|_early-onset|_with_or_without_developmental_delay": 3,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|not_provided": 2,
    "Inborn_genetic_diseases|Epilepsy|_early-onset|_with_or_without_developmental_delay|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 3,
    "not_provided|SETD1A-related_disorder": 7,
    "Inborn_genetic_diseases|Epilepsy|_early-onset|_with_or_without_developmental_delay|SETD1A-related_disorder": 1,
    "SETD1A-related_disorder|Epilepsy|_early-onset|_with_or_without_developmental_delay|Inborn_genetic_diseases": 1,
    "SETD1A-related_disorder|Inborn_genetic_diseases": 3,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 1,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|Epilepsy|_early-onset|_with_or_without_developmental_delay": 2,
    "not_provided|Epilepsy|_early-onset|_with_or_without_developmental_delay": 4,
    "See_cases|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 1,
    "Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|not_provided|Epilepsy|_early-onset|_with_or_without_developmental_delay": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Epilepsy|_early-onset|_with_or_without_developmental_delay": 1,
    "Inborn_genetic_diseases|SETD1A-related_disorder|not_provided": 1,
    "SETD1A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|Epilepsy|_early-onset|_with_or_without_developmental_delay|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 1,
    "SETD1A-related_disorder|Inborn_genetic_diseases|not_provided|Epilepsy|_early-onset|_with_or_without_developmental_delay": 1,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay|not_provided": 1,
    "Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "Epilepsy|_early-onset|_with_or_without_developmental_delay|not_provided|Neurodevelopmental_disorder_with_speech_impairment_and_dysmorphic_facies": 1,
    "HSD3B7-related_disorder": 21,
    "Inborn_genetic_diseases|HSD3B7-related_disorder|not_provided": 1,
    "Congenital_bile_acid_synthesis_defect|HSD3B7-related_disorder|not_provided|Congenital_bile_acid_synthesis_defect_1": 1,
    "not_provided|HSD3B7-related_disorder": 6,
    "Congenital_bile_acid_synthesis_defect_1": 12,
    "HSD3B7-related_disorder|not_provided": 4,
    "not_provided|HSD3B7-related_disorder|Inborn_genetic_diseases": 2,
    "Congenital_bile_acid_synthesis_defect_1|not_provided": 3,
    "not_provided|Congenital_bile_acid_synthesis_defect_1": 3,
    "HSD3B7-related_disorder|Congenital_bile_acid_synthesis_defect_1|not_provided": 1,
    "HSD3B7-related_disorder|not_provided|Inborn_genetic_diseases|Congenital_bile_acid_synthesis_defect_1": 1,
    "Inborn_genetic_diseases|HSD3B7-related_disorder": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_1|not_specified": 1,
    "not_provided|Congenital_bile_acid_synthesis_defect_1|HSD3B7-related_disorder": 1,
    "Congenital_bile_acid_synthesis_defect_1|not_provided|not_specified": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 263,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 21,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 2,
    "Inborn_genetic_diseases|STX1B-related_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|STX1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "STX1B-related_disorder|not_provided|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|STX1B-related_disorder|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_provided": 13,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_9|STX1B-related_disorder|not_provided": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_9|Inborn_genetic_diseases": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|STX1B-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|See_cases": 1,
    "Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_provided": 2,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 3,
    "STX1B-related_disorder|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 1,
    "not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 3,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|STX1B-related_disorder": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_specified": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_specified|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_9|not_provided|Inborn_genetic_diseases": 1,
    "STX1B-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_9": 1,
    "Sensorineural_hearing_loss_disorder|Hearing_loss|_autosomal_recessive_123": 1,
    "ZNF668-related_disorder|not_provided": 1,
    "ZNF668-related_disorder": 4,
    "Neurodevelopmental_disorder_with_poor_growth": 1,
    "marked_facial_dysmorphism|Profound_global_developmental_delay|Progressive_microcephaly|Failure_to_thrive|Neurodevelopmental_disorder_with_poor_growth|_large_ears|_and_dysmorphic_facies": 1,
    "Severe_short-limb_dwarfism|marked_facial_dysmorphism|Profound_global_developmental_delay|Progressive_microcephaly|Failure_to_thrive|Neurodevelopmental_disorder_with_poor_growth|_large_ears|_and_dysmorphic_facies": 1,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2": 17,
    "warfarin_response_-_Dosage|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2": 1,
    "not_provided|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2": 2,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2|Hereditary_combined_deficiency_of_vitamin_K-dependent_clotting_factors": 1,
    "not_provided|warfarin_response_-_Dosage": 1,
    "VKORC1-related_disorder": 4,
    "VKORC1-related_disorder|not_provided": 1,
    "not_specified|warfarin_response_-_Dosage": 1,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2|Warfarin_response": 1,
    "not_provided|not_specified|Vitamin_K-Dependent_Clotting_Factors|Warfarin_response|warfarin_response_-_Dosage|phenprocoumon_response_-_Dosage|acenocoumarol_response_-_Dosage": 1,
    "Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2|not_provided": 1,
    "Thrombus|VKORC1-related_disorder|not_specified|not_provided|Warfarin_response|Vitamin_K-dependent_clotting_factors|_combined_deficiency_of|_type_2|warfarin_response_-_Dosage": 1,
    "Thrombus|Venous_thromboembolism|VKORC1-related_disorder|not_specified|not_provided|Warfarin_response|warfarin_response_-_Dosage|phenprocoumon_response_-_Dosage|acenocoumarol_response_-_Dosage|warfarin_response_-_Efficacy|phenprocoumon_response_-_Toxicity|warfarin_response_-_Toxicity|See_cases": 1,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency": 65,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|Inborn_genetic_diseases": 4,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|BCKDK-related_disorder": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency": 1,
    "not_provided|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency": 9,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|not_provided": 3,
    "Inborn_genetic_diseases|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency": 3,
    "BCKDK-related_disorder": 4,
    "Inborn_genetic_diseases|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|not_provided": 1,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|not_provided|not_specified": 1,
    "not_specified|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|not_provided": 2,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|not_specified": 1,
    "not_provided|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency": 1,
    "BCKDK-related_disorder|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency": 1,
    "not_provided|Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|not_specified": 1,
    "Branched-chain_keto_acid_dehydrogenase_kinase_deficiency|BCKDK-related_disorder|not_provided": 1,
    "not_provided|BCKDK-related_disorder": 1,
    "Li-Ghorbani-Weisz-Hubshman_syndrome": 18,
    "Li-Ghorbani-Weisz-Hubshman_syndrome|Inborn_genetic_diseases": 2,
    "KAT8-related_disorder": 6,
    "Inborn_genetic_diseases|KAT8-related_disorder": 1,
    "not_provided|Li-Ghorbani-Weisz-Hubshman_syndrome": 1,
    "Amyotrophic_lateral_sclerosis_type_6|not_provided": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_6": 2,
    "FUS-related_disorder": 22,
    "FUS-related_disorder|not_provided": 2,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 162,
    "Amyotrophic_lateral_sclerosis_type_6|Dystonic_disorder|Myoclonus": 1,
    "FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 4,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder|Inborn_genetic_diseases": 2,
    "Amyotrophic_lateral_sclerosis_type_6|FUS-related_disorder|Tremor|_hereditary_essential|_4": 1,
    "Inborn_genetic_diseases|not_provided|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 2,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 9,
    "Inborn_genetic_diseases|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 3,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|Inborn_genetic_diseases|not_provided": 6,
    "FUS-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 3,
    "not_provided|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_specified": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_specified": 1,
    "not_provided|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|Inborn_genetic_diseases": 1,
    "Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6": 17,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided": 7,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_specified|not_provided": 1,
    "FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|Inborn_genetic_diseases": 5,
    "FUS-related_disorder|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder|not_provided|not_specified": 1,
    "Tremor|_hereditary_essential|_4|not_specified|Amyotrophic_lateral_sclerosis_type_6|not_provided": 1,
    "FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 2,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_specified|FUS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_6|FUS-related_disorder|Tremor|_hereditary_essential|_4": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6": 3,
    "Inborn_genetic_diseases|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6": 5,
    "Tremor|_hereditary_essential|_4": 3,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided|Inborn_genetic_diseases|FUS-related_disorder": 1,
    "FUS-related_disorder|not_specified|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder": 3,
    "Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_provided|FUS-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided|not_specified|FUS-related_disorder": 1,
    "Inborn_genetic_diseases|FUS-related_disorder|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided|not_specified|Amyotrophic_Lateral_Sclerosis|_Dominant|FUS-related_disorder": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder": 1,
    "FUS-related_disorder|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|FUS-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 1,
    "FUS-related_disorder|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_provided|Inborn_genetic_diseases": 1,
    "Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|FUS-related_disorder": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_specified": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided": 1,
    "FUS-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided|FUS-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 6,
    "Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_provided": 1,
    "Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|Inborn_genetic_diseases": 1,
    "Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_provided|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder|not_provided": 1,
    "FUS-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|Inborn_genetic_diseases|not_specified": 1,
    "Amyotrophic_lateral_sclerosis|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|FUS-related_disorder|not_provided|Inborn_genetic_diseases|Frontotemporal_dementia": 1,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6": 1,
    "not_specified|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 1,
    "Amyotrophic_lateral_sclerosis_type_6|FUS-related_disorder|not_provided|Tremor|_hereditary_essential|_4": 1,
    "not_provided|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided|FUS-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 1,
    "Amyotrophic_lateral_sclerosis_6|_autosomal_recessive": 1,
    "FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|not_provided|Tremor|_hereditary_essential|_4": 1,
    "not_provided|FUS-related_disorder|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4": 2,
    "Amyotrophic_lateral_sclerosis_type_6|not_provided|Tremor|_hereditary_essential|_4": 1,
    "FUS-related_disorder|Juvenile_amyotrophic_lateral_sclerosis|Tremor|_hereditary_essential|_4|Amyotrophic_lateral_sclerosis_type_6|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_6|Tremor|_hereditary_essential|_4|FUS-related_disorder|not_provided": 1,
    "Amyotrophic_Lateral_Sclerosis|_Dominant": 8,
    "ITGAM-related_disorder|not_provided": 14,
    "not_provided|ITGAM-related_disorder": 8,
    "ITGAM-related_disorder": 5,
    "not_specified|not_provided|ITGAM-related_disorder": 1,
    "COX6A2-related_disorder": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_18|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_18": 1,
    "COX6A2-related_disorder|not_provided": 1,
    "ACTH-independent_macronodular_adrenal_hyperplasia_2": 27,
    "ARMC5-related_disorder": 52,
    "Inborn_genetic_diseases|ARMC5-related_disorder": 8,
    "not_provided|ARMC5-related_disorder": 6,
    "ARMC5-related_disorder|not_provided": 12,
    "not_provided|ACTH-independent_macronodular_adrenal_hyperplasia_2": 3,
    "ACTH-independent_macronodular_adrenal_hyperplasia_2|not_provided": 1,
    "not_specified|ARMC5-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|ARMC5-related_disorder": 1,
    "not_provided|ARMC5-related_disorder|Inborn_genetic_diseases": 1,
    "Cushing_syndrome_due_to_macronodular_adrenal_hyperplasia": 1,
    "ARMC5-related_disorder|Inborn_genetic_diseases": 1,
    "ARMC5-related_disorder|ACTH-independent_macronodular_adrenal_hyperplasia_2": 1,
    "Macronodular_adrenal_hyperplasia": 1,
    "ARMC5-related_disorder|not_provided|ACTH-independent_macronodular_adrenal_hyperplasia_2|not_specified": 1,
    "Inborn_genetic_diseases|ACTH-independent_macronodular_adrenal_hyperplasia_2": 1,
    "Familial_renal_glucosuria": 189,
    "Familial_renal_glucosuria|not_provided": 7,
    "Familial_renal_glucosuria|Inborn_genetic_diseases": 16,
    "SLC5A2-related_disorder": 12,
    "Familial_renal_glucosuria|not_provided|SLC5A2-related_disorder": 2,
    "not_provided|Familial_renal_glucosuria": 14,
    "Inborn_genetic_diseases|Familial_renal_glucosuria": 8,
    "SLC5A2-related_disorder|not_provided|Familial_renal_glucosuria|Prostate_cancer": 1,
    "Familial_renal_glucosuria|not_provided|Inborn_genetic_diseases": 2,
    "SLC5A2-related_disorder|not_provided|Familial_renal_glucosuria": 2,
    "Inborn_genetic_diseases|not_provided|Familial_renal_glucosuria": 1,
    "SLC5A2-related_disorder|Familial_renal_glucosuria": 1,
    "not_provided|Familial_renal_glucosuria|See_cases": 1,
    "Familial_renal_glucosuria|Inborn_genetic_diseases|not_provided": 1,
    "SLC5A2-related_disorder|not_provided": 1,
    "Familial_renal_glucosuria|SLC5A2-related_disorder": 1,
    "not_specified|Familial_renal_glucosuria": 1,
    "C16orf58-related_condition": 1,
    "Familial_renal_glucosuria|not_provided|not_specified|SLC5A2-related_disorder": 1,
    "AHSP-related_disorder": 2,
    "AHSP-related_disorder|not_provided": 1,
    "Parkinson_disease_17": 136,
    "Parkinson_disease_17|not_provided": 7,
    "not_provided|Parkinson_disease_17": 13,
    "VPS35-related_disorder|Parkinson_disease_17|not_provided": 1,
    "VPS35-related_disorder|not_provided|Parkinson_disease_17": 2,
    "not_provided|Parkinson_disease_17|not_specified": 1,
    "Inborn_genetic_diseases|Parkinson_disease_17": 3,
    "VPS35-related_disorder": 4,
    "Parkinson_disease_17|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Parkinson_disease_17|not_provided": 1,
    "Parkinson_disease|Parkinson_disease_17": 1,
    "Inborn_genetic_diseases|VPS35-related_disorder": 1,
    "not_provided|Parkinson_disease_17|Meier-Gorlin_syndrome": 1,
    "Meier-Gorlin_syndrome_3|Meier-Gorlin_syndrome|Parkinson_Disease|_Dominant|not_specified": 1,
    "not_provided|Meier-Gorlin_syndrome_3|not_specified|Parkinson_Disease|_Dominant|Meier-Gorlin_syndrome": 1,
    "Meier-Gorlin_syndrome_3": 27,
    "ORC6-related_disorder|not_provided|Meier-Gorlin_syndrome_3": 1,
    "Inborn_genetic_diseases|Meier-Gorlin_syndrome_3": 1,
    "not_provided|Meier-Gorlin_syndrome_3": 9,
    "not_provided|Meier-Gorlin_syndrome_3|Inborn_genetic_diseases": 1,
    "Meier-Gorlin_syndrome_3|Inborn_genetic_diseases": 1,
    "not_provided|ORC6-related_disorder": 3,
    "not_provided|not_specified|Meier-Gorlin_syndrome_3": 1,
    "not_provided|Inborn_genetic_diseases|Meier-Gorlin_syndrome_3": 1,
    "not_specified|not_provided|Meier-Gorlin_syndrome_3": 1,
    "not_provided|Meier-Gorlin_syndrome": 4,
    "MYLK3-related_disorder|not_provided": 1,
    "MYLK3-related_disorder": 1,
    "MYLK3-associated_cardiomyopathy": 1,
    "Glutamate_pyruvate_transaminase_2_deficiency": 25,
    "Inborn_genetic_diseases|Glutamate_pyruvate_transaminase_2_deficiency": 4,
    "Intellectual_disability|_mild|Aggressive_behavior|Frequent_falls|Delayed_speech_and_language_development": 1,
    "Inborn_genetic_diseases|Glutamate_pyruvate_transaminase_2_deficiency|GPT2-related_neurodevelopmental_disorder": 1,
    "not_provided|GPT2-related_disorder": 1,
    "GPT2-related_disorder": 2,
    "Inborn_genetic_diseases|GPT2-related_disorder": 1,
    "GPT2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Glutamate_pyruvate_transaminase_2_deficiency|not_provided": 1,
    "not_provided|Glutamate_pyruvate_transaminase_2_deficiency": 1,
    "Glutamate_pyruvate_transaminase_2_deficiency|Inborn_genetic_diseases": 1,
    "Glutamate_pyruvate_transaminase_2_deficiency|not_provided": 2,
    "GPT2-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Glutamate_pyruvate_transaminase_2_deficiency|Hereditary_spastic_paraplegia_73": 1,
    "PHKB-related_disorder|not_specified": 1,
    "Glycogen_storage_disease_IXb|not_specified": 14,
    "Glycogen_storage_disease_IXb": 800,
    "Glycogen_storage_disease_IXb|not_provided": 12,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXb": 24,
    "not_specified|PHKB-related_disorder|not_provided|Glycogen_storage_disease_IXb": 1,
    "Glycogen_storage_disease_IXb|Inborn_genetic_diseases": 26,
    "Glycogen_storage_disease_IXb|PHKB-related_disorder": 3,
    "Glycogen_storage_disease_IXb|Glycogen_phosphorylase_kinase_deficiency": 4,
    "not_provided|Glycogen_storage_disease_IXb": 19,
    "PHKB-related_disorder|Glycogen_storage_disease_IXb|Glycogen_phosphorylase_kinase_deficiency": 2,
    "Glycogen_storage_disease_IXb|Inborn_genetic_diseases|not_provided": 4,
    "Glycogen_storage_disease_IXb|PHKB-related_disorder|not_specified": 1,
    "not_specified|Glycogen_storage_disease_IXb": 15,
    "Glycogen_phosphorylase_kinase_deficiency|Glycogen_storage_disease_IXb|not_provided": 1,
    "Glycogen_storage_disease_IXb|not_specified|not_provided": 2,
    "not_specified|not_provided|Glycogen_storage_disease_IXb": 3,
    "not_provided|PHKB-related_disorder|Glycogen_storage_disease_IXb": 4,
    "not_provided|not_specified|PHKB-related_disorder|Glycogen_storage_disease_IXb": 1,
    "PHKB-related_disorder|not_provided|Glycogen_storage_disease_IXb": 1,
    "not_specified|Glycogen_storage_disease_IXb|PHKB-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_IXb": 1,
    "not_specified|Glycogen_storage_disease_IXb|not_provided": 2,
    "not_provided|Glycogen_storage_disease_IXb|not_specified": 3,
    "PHKB-related_disorder|Glycogen_phosphorylase_kinase_deficiency|Glycogen_storage_disease_IXb": 1,
    "Glycogen_storage_disease_IXb|not_provided|Inborn_genetic_diseases": 1,
    "Glycogen_phosphorylase_kinase_deficiency|not_provided|Glycogen_storage_disease_IXb": 1,
    "not_provided|Glycogen_storage_disease_IXb|Inborn_genetic_diseases": 3,
    "PHKB-related_disorder": 4,
    "Inborn_genetic_diseases|PHKB-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_IXb": 1,
    "PHKB-related_disorder|not_specified|not_provided|Glycogen_storage_disease_IXb": 1,
    "Glycogen_storage_disease_IXb|See_cases|not_provided": 1,
    "PHKB-related_disorder|Glycogen_storage_disease_IXb": 2,
    "Glycogen_storage_disease_IXb|not_provided|PHKB-related_disorder": 2,
    "Glycogen_storage_disease_IXb|not_provided|not_specified": 1,
    "not_provided|Glycogen_storage_disease_IXb|PHKB-related_disorder": 2,
    "not_provided|not_specified|Glycogen_storage_disease_IXb": 3,
    "PHKB-related_disorder|Glycogen_storage_disease_IXb|not_provided|Glycogen_phosphorylase_kinase_deficiency": 1,
    "Glycogen_storage_disease_IXb|Mitochondrial_disease|not_specified": 1,
    "not_specified|not_provided|Glycogen_storage_disease_IXb|Glycogen_phosphorylase_kinase_deficiency": 1,
    "Glycogen_phosphorylase_kinase_deficiency|Glycogen_storage_disease_IXb": 1,
    "Glycogen_phosphorylase_kinase_deficiency|not_provided": 4,
    "APOCRINE_GLAND_SECRETION|_VARIATION_IN": 2,
    "ABCC11-related_condition": 1,
    "APOCRINE_GLAND_SECRETION|_VARIATION_IN|Axillary_odor|Colostrum_secretion|not_provided": 1,
    "Buratti-Harel_syndrome": 12,
    "not_provided|SIAH1-related_condition": 1,
    "Buratti-Harel_syndrome|Neurodevelopmental_disorder": 1,
    "SIAH1-related_condition": 1,
    "Buratti-Harel_syndrome|See_cases": 1,
    "Nephronophthisis_14": 628,
    "not_provided|ZNF423-related_disorder|Nephronophthisis_14": 2,
    "Nephronophthisis_14|not_specified": 39,
    "Joubert_syndrome_19": 2,
    "not_specified|not_provided|Nephronophthisis_14": 20,
    "Optic_atrophy|Nephronophthisis_14": 1,
    "ZNF423-related_disorder|Nephronophthisis_14": 10,
    "not_specified|Nephronophthisis_14": 23,
    "ZNF423-related_disorder|not_specified|Nephronophthisis_14": 1,
    "Nephronophthisis_14|ZNF423-related_disorder": 13,
    "Nephronophthisis_14|not_provided": 12,
    "not_provided|Nephronophthisis_14": 21,
    "not_provided|not_specified|Nephronophthisis_14": 6,
    "Nephronophthisis_14|Abnormal_brain_morphology": 1,
    "ZNF423-related_disorder|not_specified|not_provided|Nephronophthisis_14": 1,
    "not_provided|Nephronophthisis_14|not_specified": 7,
    "Nephronophthisis_14|not_provided|not_specified": 2,
    "not_provided|Nephronophthisis_14|ZNF423-related_disorder": 2,
    "Tibial_muscular_dystrophy|Nephronophthisis_14|not_specified": 1,
    "Retinal_dystrophy|Nephronophthisis_14|Optic_atrophy": 1,
    "Retinal_dystrophy|not_specified|Nephronophthisis_14": 1,
    "not_specified|Nephronophthisis_14|not_provided": 3,
    "Optic_atrophy|Retinal_dystrophy|Nephronophthisis_14|ZNF423-related_disorder": 1,
    "not_specified|Nephronophthisis_14|ZNF423-related_disorder": 1,
    "Nephronophthisis_14|Chronic_kidney_disease": 1,
    "ZNF423-related_disorder|not_provided|Nephronophthisis_14": 3,
    "ZNF423-related_disorder|Nephronophthisis_14|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "not_provided|not_specified|ZNF423-related_disorder|Nephronophthisis_14": 1,
    "Nephronophthisis_14|ZNF423-related_disorder|not_specified": 1,
    "Nephronophthisis_14|not_provided|ZNF423-related_disorder": 2,
    "Nephronophthisis_14|not_specified|not_provided": 5,
    "Nephronophthisis_14|Ciliopathy": 1,
    "Nephronophthisis_14|not_provided|Optic_atrophy": 1,
    "ZNF423-related_disorder": 2,
    "ZNF423-related_disorder|Nephronophthisis_14|not_provided|not_specified": 1,
    "Abnormal_brain_morphology|Nephronophthisis_14": 1,
    "not_specified|ZNF423-related_disorder|not_provided|Nephronophthisis_14": 1,
    "Diamond-Blackfan_anemia_21": 4,
    "Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia_21": 2,
    "Diamond-Blackfan_anemia_21|Diamond-Blackfan_anemia_1": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_21": 2,
    "TENT4B-related_disorder": 2,
    "Granular_cell_cancer": 1,
    "Blau_syndrome": 36,
    "Crohn_disease|Blau_syndrome": 2,
    "not_specified|not_provided|Inflammatory_bowel_disease_1|Blau_syndrome": 1,
    "Inflammatory_bowel_disease_1|Blau_syndrome": 23,
    "Inflammatory_bowel_disease_1|not_provided|Blau_syndrome": 2,
    "Regional_enteritis|Blau_syndrome": 364,
    "not_provided|Regional_enteritis|Blau_syndrome": 13,
    "Blau_syndrome|Regional_enteritis": 258,
    "Blau_syndrome|Regional_enteritis|Inborn_genetic_diseases": 8,
    "Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1": 1,
    "NOD2-related_disorder|Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome": 7,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome|not_specified|not_provided": 2,
    "Regional_enteritis|Blau_syndrome|Yao_syndrome": 1,
    "Regional_enteritis|Blau_syndrome|not_provided": 17,
    "NOD2-related_disorder|Regional_enteritis|Blau_syndrome": 3,
    "Regional_enteritis|Blau_syndrome|not_provided|Inflammatory_bowel_disease_1|Yao_syndrome": 1,
    "Behcet_disease|Regional_enteritis|Blau_syndrome": 1,
    "Regional_enteritis|Blau_syndrome|Inborn_genetic_diseases": 16,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1": 6,
    "Inborn_genetic_diseases|Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome": 1,
    "not_provided|Blau_syndrome|Regional_enteritis": 12,
    "Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|Regional_enteritis": 2,
    "Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome": 8,
    "Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome|not_provided": 5,
    "NOD2-related_disorder|Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|not_provided": 22,
    "Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|Yao_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Blau_syndrome|Regional_enteritis": 9,
    "Autoinflammatory_syndrome|Blau_syndrome|Inflammatory_bowel_disease_1|not_provided|Regional_enteritis": 1,
    "NOD2-related_disorder|Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|not_specified|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome|not_provided": 4,
    "Blau_syndrome|Regional_enteritis|not_specified|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1": 7,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|not_specified|not_provided": 2,
    "Autoinflammatory_syndrome|not_provided|Inflammatory_bowel_disease_1|Blau_syndrome|Regional_enteritis": 1,
    "NOD2-related_disorder|Autoinflammatory_syndrome|not_provided|Regional_enteritis|Blau_syndrome": 1,
    "Inborn_genetic_diseases|NOD2-related_disorder|Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1": 1,
    "Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome|Inborn_genetic_diseases": 1,
    "Regional_enteritis|Blau_syndrome|not_specified|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided|Inflammatory_bowel_disease_1": 1,
    "not_provided|Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome": 1,
    "Blau_syndrome|Inflammatory_bowel_disease_1": 13,
    "Blau_syndrome|Regional_enteritis|Inborn_genetic_diseases|not_provided|Inflammatory_bowel_disease_1": 1,
    "not_provided|Blau_syndrome|Regional_enteritis|not_specified": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|NOD2-related_disorder|Inflammatory_bowel_disease_1|Yao_syndrome": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|NOD2-related_disorder": 1,
    "NOD2-related_disorder": 6,
    "Inflammatory_bowel_disease_1|Noonan_syndrome_1": 1,
    "Autoinflammatory_syndrome|not_provided|Blau_syndrome|Regional_enteritis": 1,
    "Inflammatory_bowel_disease_1|Yao_syndrome|Blau_syndrome|Regional_enteritis|not_provided": 1,
    "Inborn_genetic_diseases|Regional_enteritis|Blau_syndrome": 6,
    "Blau_syndrome|Regional_enteritis|Inborn_genetic_diseases|not_specified": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases": 4,
    "Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|not_provided": 3,
    "not_provided|Autoinflammatory_syndrome|Blau_syndrome|Regional_enteritis": 1,
    "Inflammatory_bowel_disease_1|Regional_enteritis|Blau_syndrome": 2,
    "Yao_syndrome": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Inborn_genetic_diseases|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Inflammatory_bowel_disease_1|NOD2-related_disorder|Blau_syndrome|Regional_enteritis": 1,
    "not_provided|Blau_syndrome": 2,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1": 1,
    "NOD2-related_disorder|Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|Regional_enteritis|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome": 8,
    "not_specified|Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|Yao_syndrome": 1,
    "Yao_syndrome|Blau_syndrome|Psoriatic_arthritis|_susceptibility_to|Inflammatory_bowel_disease_1|Regional_enteritis": 1,
    "Autoinflammatory_syndrome|not_provided|Regional_enteritis|Blau_syndrome": 5,
    "Autoinflammatory_syndrome|Blau_syndrome|Regional_enteritis|not_provided": 3,
    "Blau_syndrome|Yao_syndrome|Inflammatory_bowel_disease_1|Regional_enteritis": 2,
    "Regional_enteritis|Blau_syndrome|not_specified": 1,
    "Yao_syndrome|Inflammatory_bowel_disease_1|Blau_syndrome|Regional_enteritis|Inborn_genetic_diseases": 1,
    "not_provided|Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome": 2,
    "NOD2-related_disorder|Inflammatory_bowel_disease_1|Blau_syndrome|Yao_syndrome|Regional_enteritis|not_provided": 1,
    "Inflammatory_bowel_disease_1|Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome|not_provided|NOD2-related_disorder|not_specified": 1,
    "Blau_syndrome|Regional_enteritis|not_provided|Yao_syndrome|Inflammatory_bowel_disease_1": 1,
    "not_provided|Regional_enteritis|Blau_syndrome|Inborn_genetic_diseases": 1,
    "Inflammatory_bowel_disease_1|NOD2-related_disorder|Autoinflammatory_syndrome|not_provided|Regional_enteritis|Blau_syndrome": 2,
    "Autoinflammatory_syndrome|NOD2-related_disorder|Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|not_provided": 5,
    "Autoinflammatory_syndrome|not_provided|Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1": 1,
    "Inflammatory_bowel_disease_1|not_provided|Regional_enteritis|Blau_syndrome": 4,
    "NOD2-related_disorder|not_provided|Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|not_provided": 1,
    "Inflammatory_bowel_disease_1|not_specified|not_provided|Regional_enteritis|Blau_syndrome": 2,
    "not_specified|Regional_enteritis|Blau_syndrome": 3,
    "Autoinflammatory_syndrome|Blau_syndrome|Regional_enteritis": 6,
    "Regional_enteritis|Blau_syndrome|Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|Blau_syndrome|Regional_enteritis": 1,
    "Inborn_genetic_diseases|Regional_enteritis|Blau_syndrome|not_provided": 1,
    "Yao_syndrome|Inflammatory_bowel_disease_1|Blau_syndrome": 1,
    "Blau_syndrome|Regional_enteritis|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|Regional_enteritis|Blau_syndrome|Crohn_disease": 1,
    "Inflammatory_bowel_disease_1|Yao_syndrome|Blau_syndrome|Regional_enteritis": 2,
    "Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|Blau_syndrome|Regional_enteritis|not_provided": 1,
    "not_specified|Blau_syndrome|Regional_enteritis": 1,
    "Inflammatory_bowel_disease_1|Blau_syndrome|Regional_enteritis": 3,
    "NOD2-related_disorder|Blau_syndrome|Regional_enteritis": 2,
    "Blau_syndrome|Regional_enteritis|NOD2-related_disorder|Inflammatory_bowel_disease_1|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Inflammatory_bowel_disease_1|Blau_syndrome|Regional_enteritis": 1,
    "Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|Psoriatic_arthritis|_susceptibility_to|Yao_syndrome|not_provided": 1,
    "NOD2-related_disorder|Regional_enteritis|Blau_syndrome|Crohn_disease": 1,
    "NOD2-related_disorder|Inflammatory_bowel_disease_1|Regional_enteritis|Blau_syndrome": 1,
    "Inflammatory_bowel_disease_1|NOD2-related_disorder|Blau_syndrome": 1,
    "Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome|not_specified": 1,
    "Inflammatory_bowel_disease_1|Blau_syndrome|not_specified|not_provided|Regional_enteritis|Autoinflammatory_syndrome": 1,
    "NOD2-related_disorder|Blau_syndrome|Regional_enteritis|not_provided|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|Psoriatic_arthritis|_susceptibility_to|Yao_syndrome|Inflammatory_bowel_disease_1|not_specified|NOD2-related_disorder|not_provided": 1,
    "Inflammatory_bowel_disease_1|Yao_syndrome|Blau_syndrome|Autoinflammatory_syndrome|Regional_enteritis|Crohn_disease|not_specified|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Regional_enteritis|Blau_syndrome|not_specified|Inflammatory_bowel_disease_1|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|NOD2-related_disorder": 2,
    "Blau_syndrome|Regional_enteritis|NOD2-related_disorder|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Autoinflammatory_syndrome|Yao_syndrome|Blau_syndrome|Inflammatory_bowel_disease_1|not_provided|Regional_enteritis": 1,
    "Blau_syndrome|Regional_enteritis|Yao_syndrome|Inflammatory_bowel_disease_1": 1,
    "Blau_syndrome|Regional_enteritis|NOD2-related_disorder": 2,
    "Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|Psoriatic_arthritis|_susceptibility_to|Regional_enteritis": 1,
    "Autoinflammatory_syndrome|Blau_syndrome|Regional_enteritis|not_provided|Inflammatory_bowel_disease_1|NOD2-related_disorder": 1,
    "not_provided|Blau_syndrome|Regional_enteritis|Inborn_genetic_diseases": 1,
    "NOD2-related_disorder|not_provided|Blau_syndrome|Regional_enteritis|Psoriatic_arthritis|_susceptibility_to|Yao_syndrome|Inflammatory_bowel_disease_1|Autoinflammatory_syndrome": 1,
    "NOD2-related_disorder|Inborn_genetic_diseases|Regional_enteritis|Blau_syndrome": 1,
    "Inflammatory_bowel_disease_1|NOD2-related_disorder|not_provided|Blau_syndrome": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|not_specified": 1,
    "Yao_syndrome|Blau_syndrome|Inflammatory_bowel_disease_1": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|not_provided": 1,
    "Inflammatory_bowel_disease_1|Yao_syndrome|Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|Blau_syndrome|Regional_enteritis|Inflammatory_bowel_disease_1|not_specified|not_provided": 1,
    "not_specified|Autoinflammatory_syndrome|Regional_enteritis|Blau_syndrome": 1,
    "not_provided|Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome": 2,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|NOD2-related_disorder|Inborn_genetic_diseases": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|not_provided": 1,
    "Autoinflammatory_syndrome|Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|Regional_enteritis|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|Inborn_genetic_diseases|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|not_provided": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|Psoriatic_arthritis|_susceptibility_to|not_provided": 1,
    "Inflammatory_bowel_disease_1|Yao_syndrome|Blau_syndrome|Autoinflammatory_syndrome|Regional_enteritis|Psoriatic_arthritis|_susceptibility_to|not_specified|not_provided": 1,
    "Inflammatory_bowel_disease_1|not_provided|Blau_syndrome|Regional_enteritis": 1,
    "Inflammatory_bowel_disease_1|Inborn_genetic_diseases|Blau_syndrome": 1,
    "Regional_enteritis|Blau_syndrome|Inflammatory_bowel_disease_1|NOD2-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|NOD2-related_disorder|Blau_syndrome|Regional_enteritis": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|Yao_syndrome|not_provided": 1,
    "Blau_syndrome|Regional_enteritis|Autoinflammatory_syndrome|Inflammatory_bowel_disease_1|not_specified|Psoriatic_arthritis|_susceptibility_to|Yao_syndrome|not_provided": 1,
    "Blau_syndrome|Autoinflammatory_syndrome|not_provided|Regional_enteritis|Inflammatory_bowel_disease_1": 1,
    "Inflammatory_bowel_disease_1|Blau_syndrome|Regional_enteritis|not_provided|Yao_syndrome": 1,
    "Blau_syndrome|Inflammatory_bowel_disease_1|Regional_enteritis": 1,
    "Inflammatory_bowel_disease_1|Yao_syndrome|Blau_syndrome|not_specified|Crohn_disease|Autoinflammatory_syndrome|Crohn\u2019s_Disease|Regional_enteritis|not_provided": 1,
    "not_provided|NOD2-related_disorder|Blau_syndrome|Regional_enteritis": 1,
    "NOD2-related_disorder|Regional_enteritis|Blau_syndrome|Autoinflammatory_syndrome": 1,
    "not_provided|Blau_syndrome|Inflammatory_bowel_disease_1": 3,
    "Inflammatory_bowel_disease_1|Leprosy|_susceptibility_to|_1|not_provided|Blau_syndrome": 1,
    "not_provided|Dilated_cardiomyopathy_1G|Blau_syndrome|Inflammatory_bowel_disease_1": 1,
    "Inflammatory_bowel_disease_1|Autoinflammatory_syndrome|not_provided|Blau_syndrome": 1,
    "Familial_cylindromatosis|Brooke-Spiegler_syndrome|Familial_multiple_trichoepitheliomata": 3,
    "Brooke-Spiegler_syndrome|Familial_multiple_trichoepitheliomata|Familial_cylindromatosis": 11,
    "Familial_multiple_trichoepitheliomata|Familial_cylindromatosis|Brooke-Spiegler_syndrome": 16,
    "Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 52,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8": 69,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|Familial_multiple_trichoepitheliomata|not_provided|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|Inborn_genetic_diseases": 1,
    "Familial_cylindromatosis|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|Brooke-Spiegler_syndrome|Trichoepithelioma|_multiple_familial|_1": 3,
    "Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome|not_provided|Familial_cylindromatosis": 3,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8": 4,
    "Brooke-Spiegler_syndrome|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8": 1,
    "CYLD-related_disorder": 14,
    "Familial_cylindromatosis": 21,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|not_provided": 1,
    "Brooke-Spiegler_syndrome|Familial_multiple_trichoepitheliomata|not_specified|Familial_cylindromatosis": 1,
    "Familial_cylindromatosis|not_provided": 2,
    "not_provided|Familial_multiple_trichoepitheliomata|Familial_cylindromatosis|Brooke-Spiegler_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8": 1,
    "Brooke-Spiegler_syndrome": 9,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|not_provided|Trichoepithelioma|_multiple_familial|_1|Familial_cylindromatosis|Brooke-Spiegler_syndrome": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "Familial_multiple_trichoepitheliomata|not_provided|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 5,
    "not_specified|Brooke-Spiegler_syndrome|Familial_multiple_trichoepitheliomata|Trichoepithelioma|_multiple_familial|_1|Familial_cylindromatosis": 1,
    "CYLD-related_disorder|not_provided": 1,
    "Trichoepithelioma|_multiple_familial|_1|Familial_multiple_trichoepitheliomata|not_provided|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 3,
    "CYLD-related_disorder|Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "Brooke-Spiegler_syndrome|not_provided": 1,
    "Familial_multiple_trichoepitheliomata": 3,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|not_specified": 1,
    "Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome": 1,
    "Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "not_specified|Brooke-Spiegler_syndrome|Familial_cylindromatosis|not_provided": 1,
    "not_provided|Trichoepithelioma|_multiple_familial|_1|Familial_cylindromatosis|Brooke-Spiegler_syndrome": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|SLC35A2-congenital_disorder_of_glycosylation|Familial_cylindromatosis|Brooke-Spiegler_syndrome": 1,
    "Trichoepithelioma|_multiple_familial|_2|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "not_provided|Familial_cylindromatosis|Brooke-Spiegler_syndrome|Familial_multiple_trichoepitheliomata": 1,
    "Trichoepithelioma|_multiple_familial|_1|not_provided|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "not_provided|CYLD-related_disorder": 2,
    "Familial_cylindromatosis|Brooke-Spiegler_syndrome|Trichoepithelioma|_multiple_familial|_1|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_8|not_provided|Familial_multiple_trichoepitheliomata": 1,
    "Trichoepithelioma|_multiple_familial|_2|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 4,
    "not_provided|Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 5,
    "Familial_cylindromatosis|Familial_multiple_trichoepitheliomata|Brooke-Spiegler_syndrome": 2,
    "not_provided|Brooke-Spiegler_syndrome|Familial_multiple_trichoepitheliomata|Familial_cylindromatosis": 1,
    "not_provided|Trichoepithelioma|_multiple_familial|_2|Brooke-Spiegler_syndrome|Familial_cylindromatosis": 1,
    "Townes-Brocks_syndrome_1": 78,
    "Townes-Brocks_syndrome_1|not_provided": 7,
    "SALL1-related_disorder": 29,
    "Townes_syndrome": 162,
    "not_provided|Townes_syndrome|Inborn_genetic_diseases": 2,
    "SALL1-related_disorder|Townes_syndrome|Townes-Brocks_syndrome_1|not_provided|not_specified": 1,
    "Townes_syndrome|not_specified|not_provided": 4,
    "Townes_syndrome|SALL1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Townes_syndrome": 11,
    "Townes_syndrome|not_specified|not_provided|Townes-Brocks_syndrome_1": 4,
    "Townes_syndrome|Inborn_genetic_diseases|not_provided|Townes-Brocks_syndrome_1": 1,
    "not_specified|not_provided|Townes_syndrome|Townes-Brocks_syndrome_1": 3,
    "Townes_syndrome|SALL1-related_disorder|not_specified|not_provided|Townes-Brocks_syndrome_1": 1,
    "Townes-Brocks_syndrome_1|SALL1-related_disorder|not_provided|Townes_syndrome": 1,
    "not_specified|Townes-Brocks_syndrome_1|Townes_syndrome": 2,
    "not_provided|Townes_syndrome": 15,
    "not_provided|Townes-Brocks_syndrome_1|Townes_syndrome": 1,
    "Inborn_genetic_diseases|Townes-Brocks_syndrome_1|Townes_syndrome": 1,
    "Townes_syndrome|Inborn_genetic_diseases": 9,
    "not_provided|not_specified|Inborn_genetic_diseases|Townes_syndrome": 1,
    "Townes-Brocks_syndrome_1|not_provided|Townes_syndrome": 2,
    "not_provided|SALL1-related_disorder": 5,
    "not_specified|Townes-Brocks_syndrome_1|Townes_syndrome|not_provided": 1,
    "not_provided|SALL1-related_disorder|Townes_syndrome|Inborn_genetic_diseases|Townes-Brocks_syndrome_1": 1,
    "Townes_syndrome|Townes-Brocks_syndrome_1|not_provided": 6,
    "Townes_syndrome|not_provided": 9,
    "Townes_syndrome|Inborn_genetic_diseases|SALL1-related_disorder|not_provided": 1,
    "SALL1-related_disorder|Townes-Brocks_syndrome_1|not_specified": 1,
    "SALL1-related_disorder|Townes-Brocks_syndrome_1|Townes_syndrome|not_provided": 1,
    "Townes-Brocks_syndrome_1|Townes_syndrome": 4,
    "Inborn_genetic_diseases|Townes_syndrome|Townes-Brocks_syndrome_1": 1,
    "not_provided|not_specified|Townes_syndrome|Townes-Brocks_syndrome_1": 1,
    "not_provided|Townes-Brocks_syndrome_1": 6,
    "SALL1-related_disorder|Inborn_genetic_diseases|Townes_syndrome|Townes-Brocks_syndrome_1": 1,
    "Townes_syndrome|SALL1-related_disorder|not_provided|Townes-Brocks_syndrome_1": 1,
    "Inborn_genetic_diseases|Townes_syndrome|not_provided": 1,
    "Townes-Brocks_syndrome_1|Inborn_genetic_diseases": 1,
    "Townes_syndrome|Townes-Brocks_syndrome_1": 3,
    "Townes-Brocks_syndrome_1|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "SALL1-related_disorder|Townes_syndrome": 5,
    "Townes_syndrome|SALL1-related_disorder": 4,
    "Townes_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Townes_syndrome|Townes-Brocks_syndrome_1|not_specified": 1,
    "SALL1-related_disorder|Townes_syndrome|Townes-Brocks_syndrome_1": 1,
    "Townes_syndrome|not_provided|not_specified": 2,
    "not_specified|Townes_syndrome": 2,
    "not_provided|not_specified|Townes_syndrome": 2,
    "Townes_syndrome|Townes-Brocks_syndrome_1|Inborn_genetic_diseases": 1,
    "Townes_syndrome|not_provided|Townes-Brocks_syndrome_1": 3,
    "not_provided|Townes_syndrome|not_specified": 2,
    "Townes_syndrome|Inborn_genetic_diseases|SALL1-related_disorder": 1,
    "Townes-Brocks_syndrome_1|Townes_syndrome|SALL1-related_disorder": 1,
    "SALL1-related_disorder|not_provided|Townes_syndrome": 1,
    "Townes_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Townes_syndrome": 2,
    "SALL1-related_disorder|Townes_syndrome|not_provided|not_specified": 1,
    "Townes_syndrome|Inborn_genetic_diseases|SALL1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Townes_syndrome|not_provided": 5,
    "Townes-Brocks-branchiootorenal-like_syndrome": 1,
    "SALL1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|SALL1-related_disorder": 1,
    "SALL1-related_disorder|Inborn_genetic_diseases|not_specified|Townes_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Townes-Brocks_syndrome_1": 1,
    "not_provided|Townes-Brocks_syndrome_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Townes_syndrome": 1,
    "Townes-Brocks-branchiootorenal-like_syndrome|Townes-Brocks_syndrome_1|Townes_syndrome": 1,
    "Hearing_impairment|Townes_syndrome": 1,
    "Inborn_genetic_diseases|Townes_syndrome|SALL1-related_disorder": 1,
    "Townes-Brocks_syndrome_1|not_provided|Townes_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Townes_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Townes_syndrome|VACTERL_with_hydrocephalus|not_provided|Townes-Brocks_syndrome_1": 1,
    "Townes_syndrome|Townes-Brocks_syndrome_1|SALL1-related_disorder": 1,
    "Inborn_genetic_diseases|Townes-Brocks_syndrome_1": 1,
    "SALL1-related_disorder|Townes_syndrome|not_provided": 1,
    "not_provided|Townes_syndrome|Townes-Brocks_syndrome_1": 1,
    "Townes_syndrome|not_specified|Townes-Brocks_syndrome_1|not_provided": 1,
    "Townes_syndrome|Townes-Brocks_syndrome_1|not_specified|not_provided": 1,
    "Townes_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_specified|SALL1-related_disorder|not_provided": 1,
    "Townes_syndrome|Inborn_genetic_diseases|not_provided|SALL1-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "not_provided|Townes_syndrome|not_specified|Townes-Brocks_syndrome_1": 1,
    "Townes_syndrome|SALL1-related_disorder|not_specified|not_provided": 1,
    "Townes-Brocks_syndrome_1|Townes_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Townes-Brocks_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Townes-Brocks_syndrome_1|Townes_syndrome|not_provided": 1,
    "not_specified|Townes_syndrome|SALL1-related_disorder": 1,
    "Townes_syndrome|not_provided|SALL1-related_disorder": 1,
    "Brunet-Wagner_neurodevelopmental_syndrome": 11,
    "RBL2-related_disorder|not_provided": 1,
    "Brunet-Wagner_neurodevelopmental_syndrome|not_specified": 1,
    "Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome_7": 23,
    "Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5": 17,
    "Meckel_syndrome|_type_5|not_provided|Nephronophthisis_8|Joubert_syndrome_7": 3,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 2,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|not_provided|Joubert_syndrome_7": 1,
    "Joubert_syndrome_7|Nephronophthisis_8|Meckel_syndrome|_type_5": 4,
    "not_provided|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|Nephronophthisis_8": 3,
    "Nephronophthisis_8|Joubert_syndrome_7|not_provided|Meckel_syndrome|_type_5": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3": 72,
    "Joubert_syndrome|Joubert_syndrome_7|Meckel-Gruber_syndrome|Nephronophthisis_8|not_specified|not_provided|Meckel_syndrome|_type_5": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder": 2,
    "Joubert_syndrome|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome": 6,
    "RPGRIP1L-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Nephronophthisis_8|Retinal_dystrophy|not_provided|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 33,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 6,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 8,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|not_specified|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|Meckel-Gruber_syndrome|not_provided|RPGRIP1L-related_disorder|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3": 1,
    "RPGRIP1L-related_disorder": 75,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 26,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Nephronophthisis_8": 2,
    "Inborn_genetic_diseases|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 5,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7|RPGRIP1L-related_disorder|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 8,
    "not_specified|Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "Joubert_syndrome|RPGRIP1L-related_disorder": 3,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 5,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|not_specified|not_provided|Nephronophthisis_8": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3": 5,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder": 1,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|not_specified|RPGRIP1L-related_disorder|Nephronophthisis_8|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_1": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 2,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|not_specified|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "Joubert_syndrome|RPGRIP1L-related_disorder|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Inborn_genetic_diseases|not_provided|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases|not_provided|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Joubert_syndrome_7": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 12,
    "not_provided|not_specified|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome": 10,
    "Inborn_genetic_diseases|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Nephronophthisis_8|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|RPGRIP1L-related_disorder|Meckel_syndrome|_type_5": 1,
    "COACH_syndrome_1|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|not_provided|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder|not_provided": 1,
    "Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome": 5,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_7|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "not_provided|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Nephronophthisis_8|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder": 3,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Retinal_dystrophy": 1,
    "not_provided|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|not_provided": 1,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|not_specified|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3": 2,
    "RPGRIP1L-related_disorder|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|not_specified|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Kidney_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Nephronophthisis_8": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|not_specified": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|not_provided|not_specified|Nephronophthisis_8|Kidney_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Nephronophthisis": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 2,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 17,
    "Nephronophthisis_8|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder|Retinal_dystrophy|not_provided": 1,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|not_specified|not_provided|Nephronophthisis_8|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome_and_related_disorders|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|RPGRIP1L-related_disorder|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Kidney_disorder|not_provided": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7": 5,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder": 8,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_8|not_specified|RPGRIP1L-related_disorder|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|RPGRIP1L-related_disorder|not_provided": 1,
    "Meckel_syndrome|_type_5|Inborn_genetic_diseases|Nephronophthisis_8|Joubert_syndrome_7": 2,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 4,
    "Joubert_syndrome|Microcephaly|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_1": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_7|not_specified|Nephronophthisis_8|Meckel_syndrome|_type_5": 1,
    "Joubert_syndrome_7|Joubert_syndrome|Nephronophthisis_8|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3": 1,
    "Joubert_syndrome|not_provided|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|not_provided|RPGRIP1L-related_disorder": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder|not_specified": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_specified|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided": 1,
    "not_provided|not_specified|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 2,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|not_provided|Meckel-Gruber_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|RPGRIP1L-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|RPGRIP1L-related_disorder": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7": 4,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome": 3,
    "not_provided|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3": 2,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "Meckel_syndrome|_type_5": 3,
    "Joubert_syndrome|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome": 2,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_8|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|Joubert_syndrome_7": 1,
    "RPGRIP1L-related_disorder|not_specified|not_provided|Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome_7|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome": 1,
    "COACH_syndrome_1|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder|Joubert_syndrome|not_provided|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Inborn_genetic_diseases": 4,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder": 2,
    "RPGRIP1L-related_disorder|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_7": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder": 3,
    "RPGRIP1L-related_disorder|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|not_specified|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3": 4,
    "not_provided|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 2,
    "RPGRIP1L-related_disorder|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome_7|COACH_syndrome_3|not_provided|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|RPGRIP1L-related_disorder|Joubert_syndrome_and_related_disorders|Meckel-Gruber_syndrome|not_provided|Nephronophthisis_8": 1,
    "Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3": 1,
    "Joubert_syndrome|Kidney_disorder|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder": 2,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome_7": 1,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided|Joubert_syndrome_and_related_disorders|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Kidney_disorder|Meckel-Gruber_syndrome|not_specified|not_provided|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|not_provided|Joubert_syndrome_7|Meckel_syndrome|_type_5|Inborn_genetic_diseases|RPGRIP1L-related_disorder": 1,
    "not_provided|Joubert_syndrome_and_related_disorders|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|not_provided|Nephronophthisis_8|Meckel_syndrome|_type_5|not_specified": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|RPGRIP1L-related_disorder|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|not_provided": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Inborn_genetic_diseases|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome_7|Joubert_syndrome": 1,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_1|not_provided|Abnormality_of_prenatal_development_or_birth": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_specified": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 2,
    "Joubert_syndrome_7|COACH_syndrome_3": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome_7|Meckel_syndrome|_type_5|Nephronophthisis_8|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|not_specified|RPGRIP1L-related_disorder": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|not_provided|Optic_atrophy": 1,
    "Joubert_syndrome|Kidney_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|RPGRIP1L-related_disorder|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|not_provided": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|not_provided": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 3,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_1|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Nephronophthisis_8|not_provided|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy|not_provided": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "not_provided|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Inborn_genetic_diseases|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder|Nephronophthisis_8|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|not_provided": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "RPGRIP1L-related_disorder|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "not_provided|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Nephronophthisis_8|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "not_provided|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|COACH_syndrome_1|Meckel_syndrome|_type_5": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Meckel-Gruber_syndrome|Joubert_syndrome": 3,
    "Joubert_syndrome|Inborn_genetic_diseases|not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 1,
    "not_provided|Joubert_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "RPGRIP1L-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 1,
    "Joubert_syndrome|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|RPGRIP1L-related_disorder|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome|RPGRIP1L-related_disorder|not_provided|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided": 1,
    "Joubert_syndrome|not_provided|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 1,
    "not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy": 2,
    "Joubert_syndrome|not_provided|Kidney_disorder|Joubert_syndrome_7|Meckel-Gruber_syndrome|Nephronophthisis_8|not_specified|Meckel_syndrome|_type_5": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_5": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|not_provided|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Inborn_genetic_diseases|RPGRIP1L-related_disorder": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided|RPGRIP1L-related_disorder": 1,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5": 2,
    "not_provided|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|Nephronophthisis_8|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_7|not_specified|not_provided": 1,
    "RPGRIP1L-related_disorder|Inborn_genetic_diseases|COACH_syndrome_1|Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided|Nephronophthisis_8|Meckel-Gruber_syndrome|Joubert_syndrome|Optic_atrophy": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_5|not_provided|Joubert_syndrome_7": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|Inborn_genetic_diseases|COACH_syndrome_3|RPGRIP1L-related_disorder": 1,
    "not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|Retinal_dystrophy": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "RPGRIP1L-related_disorder|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "RPGRIP1L-related_disorder|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Nephronophthisis_8": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Joubert_syndrome|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder|Joubert_syndrome|Inborn_genetic_diseases|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|RPGRIP1L-related_disorder": 1,
    "not_provided|COACH_syndrome_3|Joubert_syndrome_7|Meckel_syndrome|_type_5|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|COACH_syndrome_1|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_and_related_disorders|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Inborn_genetic_diseases|not_provided|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "RPGRIP1L-related_disorder|COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder": 2,
    "Joubert_syndrome_7|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|not_specified|not_provided|Nephronophthisis_8|Retinitis_pigmentosa_in_ciliopathies|_modifier_of|Focal_segmental_glomerulosclerosis": 1,
    "Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|Inborn_genetic_diseases|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_7|COACH_syndrome_3|not_specified|Nephronophthisis_8|Retinal_dystrophy": 1,
    "not_specified|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|Meckel-Gruber_syndrome|Retinal_dystrophy": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Joubert_syndrome|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Inborn_genetic_diseases|Meckel-Gruber_syndrome|not_provided|Nephronophthisis_8|Joubert_syndrome_7|not_specified": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|not_provided|RPGRIP1L-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|not_provided|Nephronophthisis_8|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Joubert_syndrome_7|not_specified|Meckel_syndrome|_type_5|not_provided": 1,
    "COACH_syndrome_3|Meckel_syndrome|_type_5|Joubert_syndrome_7|Joubert_syndrome|RPGRIP1L-related_disorder|not_provided|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|not_provided|Inborn_genetic_diseases": 1,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome|not_provided|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome_7": 1,
    "Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Retinal_dystrophy|not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Nephronophthisis_8": 1,
    "Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "RPGRIP1L-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Nephronophthisis_8|COACH_syndrome_1": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Nephronophthisis_8|Joubert_syndrome_7|Meckel_syndrome|_type_5|Inborn_genetic_diseases|COACH_syndrome_3|RPGRIP1L-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders|RPGRIP1L-related_disorder|Inborn_genetic_diseases": 1,
    "RPGRIP1L-related_disorder|Joubert_syndrome_7|COACH_syndrome_3|Meckel_syndrome|_type_5|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_7|Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "Nephronophthisis_8|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|Retinal_dystrophy|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome_7|Meckel_syndrome|_type_5|COACH_syndrome_3|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|RPGRIP1L-related_disorder": 1,
    "RPGRIP1L-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_5|COACH_syndrome_3|Joubert_syndrome_7": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases|not_provided|RPGRIP1L-related_disorder": 1,
    "not_provided|Meckel_syndrome|_type_5|Joubert_syndrome_7|COACH_syndrome_3|RPGRIP1L-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Ciliopathy|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "HP:0003473%3B_HP:0000508": 1,
    "Lethal_polymalformative_syndrome|_Boissel_type": 96,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Nephronophthisis|Lethal_polymalformative_syndrome|_Boissel_type": 1,
    "not_provided|Lethal_polymalformative_syndrome|_Boissel_type": 9,
    "OBESITY_(BMIQ14)|_SUSCEPTIBILITY_TO": 1,
    "Body_mass_index_quantitative_trait_locus_14": 1,
    "not_provided|Meniere_disease|Lethal_polymalformative_syndrome|_Boissel_type": 1,
    "Lethal_polymalformative_syndrome|_Boissel_type|not_provided|Inborn_genetic_diseases": 2,
    "Lethal_polymalformative_syndrome|_Boissel_type|Inborn_genetic_diseases": 1,
    "Lethal_polymalformative_syndrome|_Boissel_type|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|Lethal_polymalformative_syndrome|_Boissel_type": 1,
    "FTO-related_disorder|Lethal_polymalformative_syndrome|_Boissel_type|not_provided": 1,
    "Inborn_genetic_diseases|Lethal_polymalformative_syndrome|_Boissel_type": 1,
    "FTO-related_disorder": 1,
    "Lethal_polymalformative_syndrome|_Boissel_type|Inborn_genetic_diseases|not_provided": 1,
    "IRX5-related_disorder": 6,
    "Inborn_genetic_diseases|Craniofacial_dysplasia_-_osteopenia_syndrome": 1,
    "Craniofacial_dysplasia_-_osteopenia_syndrome": 8,
    "not_provided|Craniofacial_dysplasia_-_osteopenia_syndrome": 1,
    "Craniofacial_dysplasia_-_osteopenia_syndrome|not_provided": 1,
    "Craniofacial_dysplasia_-_osteopenia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|IRX5-related_disorder": 1,
    "IRX5-related_disorder|not_provided": 1,
    "Familial_hypokalemia-hypomagnesemia": 361,
    "Multicentric_Osteolysis-Nodulosis-Arthropathy_(MONA)_Spectrum_Disorders": 2,
    "Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 49,
    "Multicentric_osteolysis_nodulosis_arthropathy_spectrum|not_provided": 29,
    "not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 14,
    "not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum|MMP2-related_disorder": 1,
    "Multicentric_osteolysis|_nodulosis|_and_arthropathy|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 3,
    "Multicentric_osteolysis|_nodulosis|_and_arthropathy": 10,
    "not_specified|MMP2-related_disorder|not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 1,
    "MMP2-related_disorder": 2,
    "Multicentric_osteolysis_nodulosis_arthropathy_spectrum|Multicentric_osteolysis|_nodulosis|_and_arthropathy|not_provided": 1,
    "Inborn_genetic_diseases|Multicentric_osteolysis_nodulosis_arthropathy_spectrum|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 1,
    "Inborn_genetic_diseases|Multicentric_osteolysis|_nodulosis|_and_arthropathy|Multicentric_osteolysis_nodulosis_arthropathy_spectrum|not_provided": 1,
    "Multicentric_osteolysis_nodulosis_arthropathy_spectrum|not_specified|not_provided": 2,
    "Multicentric_osteolysis|_nodulosis|_and_arthropathy|not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 1,
    "MMP2-related_disorder|not_provided": 2,
    "MMP2-related_disorder|Multicentric_osteolysis_nodulosis_arthropathy_spectrum|not_provided": 1,
    "Inborn_genetic_diseases|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 2,
    "MMP2-related_disorder|not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 1,
    "not_specified|not_provided|Multicentric_osteolysis_nodulosis_arthropathy_spectrum": 1,
    "not_provided|Multicentric_osteolysis|_nodulosis|_and_arthropathy": 1,
    "SLC6A2-related_disorder|not_provided": 3,
    "SLC6A2-related_disorder": 2,
    "Neurocirculatory_asthenia": 12,
    "not_provided|SLC6A2-related_disorder": 1,
    "Neurocirculatory_asthenia|not_provided": 1,
    "DRUG_METABOLISM|_ALTERED|_CES1-RELATED": 4,
    "CES1-related_condition|not_specified": 1,
    "not_provided|clopidogrel_response_-_Efficacy|clopidogrel_response_-_Metabolism/PK": 1,
    "CES1-related_condition": 1,
    "Developmental_and_epileptic_encephalopathy|_17": 26,
    "GNAO1-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17": 6,
    "Developmental_and_epileptic_encephalopathy|not_provided|Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Neurodevelopmental_disorder_with_involuntary_movements": 1,
    "Developmental_and_epileptic_encephalopathy|_17|Developmental_and_epileptic_encephalopathy": 3,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|GNAO1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements": 5,
    "GNAO1-related_disorder": 8,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Intellectual_disability|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_17": 1,
    "not_specified|Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|Developmental_and_epileptic_encephalopathy": 2,
    "Neurodevelopmental_disorder_with_involuntary_movements|not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17": 1,
    "Developmental_and_epileptic_encephalopathy|_17|not_provided|Neurodevelopmental_disorder_with_involuntary_movements": 1,
    "GNAO1-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Dyskinesia|Chorea": 1,
    "GNAO1-related_disorder|not_provided|Neurodevelopmental_disorder_with_involuntary_movements": 1,
    "GNAO1-related_disorder|Rare_genetic_intellectual_disability|GNAO1-Related_Neurodevelopmental_Disorder|Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|Developmental_and_epileptic_encephalopathy|not_provided|Microcephaly|Abnormality_of_the_nervous_system": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_17": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements|GNAO1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Movement_disorder": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17|not_provided": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|GNAO1-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17": 1,
    "GNAO1-related_disorder|not_provided|Chorea|Dyskinesia|Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Choreoathetosis": 1,
    "Developmental_and_epileptic_encephalopathy|Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17": 1,
    "Inborn_genetic_diseases|GNAO1-related_disorder": 1,
    "GNAO1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_17|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_17|Neurodevelopmental_disorder_with_involuntary_movements|GNAO1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|Abnormality_of_the_nervous_system|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|GNAO1-related_developmental_delay-seizures-movement_disorder_spectrum|Developmental_delay|not_provided": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|not_provided": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy": 1,
    "Neurodevelopmental_disorder_with_involuntary_movements|Developmental_and_epileptic_encephalopathy|_17|GNAO1-related_developmental_delay-seizures-movement_disorder_spectrum": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|GNAO1-related_disorder": 1,
    "Spastic_paraplegia_89|_autosomal_recessive": 6,
    "Marfanoid_habitus_and_intellectual_disability|not_provided": 2,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 52,
    "Bardet-Biedl_syndrome_2": 139,
    "not_provided|Bardet-Biedl_syndrome_2": 5,
    "not_specified|not_provided|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome": 23,
    "Retinitis_pigmentosa_74|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|BBS2-related_disorder|Retinal_dystrophy": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome": 26,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases": 1,
    "BBS2-related_disorder": 33,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 15,
    "Bardet-Biedl_syndrome|BBS2-related_disorder": 16,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|BBS2-related_disorder": 3,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2": 29,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|not_specified": 1,
    "Retinal_dystrophy|BBS2-related_ciliopathy|Bardet-Biedl_syndrome_2": 1,
    "Inborn_genetic_diseases|BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder": 5,
    "Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 30,
    "Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|BBS2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|BBS2-related_disorder|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder": 7,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|not_provided": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS2-related_disorder": 1,
    "Bardet-Biedl_syndrome_2|Retinal_dystrophy|Bardet-Biedl_syndrome": 2,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|not_provided": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Retinal_dystrophy": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|BBS2-related_disorder": 5,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases|BBS2-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder|Bardet-Biedl_syndrome": 8,
    "BBS2-related_disorder|Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|BBS2-related_disorder": 3,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder": 2,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2": 2,
    "BBS2-related_disorder|Inborn_genetic_diseases": 3,
    "Bardet-Biedl_syndrome_2|BBS2-related_disorder|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 2,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 9,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS2-related_disorder": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Inborn_genetic_diseases|BBS2-related_disorder": 1,
    "BBS2-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|BBS2-related_disorder|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|Inborn_genetic_diseases": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|not_specified|not_provided|Bardet-Biedl_syndrome_1": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome|BBS2-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome|not_provided": 2,
    "BBS2-related_disorder|not_provided|Bardet-Biedl_syndrome": 1,
    "BBS2-related_ciliopathy|Bardet-Biedl_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinal_dystrophy|Retinitis_pigmentosa_74": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome_2": 2,
    "BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome": 3,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2": 8,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases|BBS2-related_disorder": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|BBS2-related_disorder|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome_2|BBS2-related_disorder|Bardet-Biedl_syndrome": 4,
    "BBS2-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome": 1,
    "not_provided|not_specified|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_2": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|BBS2-related_disorder|not_provided": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 2,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_2": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome_1|not_provided|Bardet-Biedl_syndrome|not_specified": 1,
    "BBS2-related_ciliopathy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2": 3,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome_2": 1,
    "not_provided|Bardet-Biedl_syndrome|Inborn_genetic_diseases|BBS2-related_disorder": 1,
    "Bardet-Biedl_syndrome_2|Retinal_dystrophy|Bardet-Biedl_syndrome|BBS2-related_disorder|not_provided|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome|BBS2-related_disorder": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2": 1,
    "Inborn_genetic_diseases|BBS2-related_disorder": 2,
    "not_provided|Bardet-Biedl_syndrome_2|not_specified|Bardet-Biedl_syndrome|BBS2-related_disorder|Retinitis_pigmentosa_74": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|Bardet-Biedl_syndrome": 2,
    "not_specified|Bardet-Biedl_syndrome_2|not_provided|Bardet-Biedl_syndrome": 1,
    "not_provided|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|not_specified|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|BBS2-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2": 2,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|BBS2-related_disorder": 2,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|BBS2-related_disorder": 1,
    "BBS2-related_ciliopathy|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|BBS2-related_disorder|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Retinal_dystrophy": 1,
    "Autosomal_recessive_retinitis_pigmentosa|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-biedl_syndrome_2/4|_digenic|Bardet-Biedl_syndrome|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome_2|Retinal_dystrophy": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Retinal_dystrophy|not_specified|not_provided|Bardet-Biedl_syndrome_2": 1,
    "BBS2-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|not_provided": 1,
    "BBS2-related_disorder|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome": 1,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_1|not_provided": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome_2|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_74|BBS2-related_disorder|Bardet-Biedl_syndrome": 1,
    "BBS2-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome|BBS2-related_disorder|Bardet-Biedl_syndrome_2": 2,
    "Retinitis_pigmentosa_74|not_provided|Bardet-Biedl_syndrome_2|not_specified": 1,
    "BBS2-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|not_provided|Bardet-Biedl_syndrome|BBS2-related_disorder": 1,
    "Retinitis_pigmentosa|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BARDET-BIEDL_SYNDROME_2/6|_DIGENIC|Bardet-Biedl_syndrome|Retinal_dystrophy": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome|not_specified|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome_1|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|not_provided|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinal_dystrophy|Retinitis_pigmentosa_74|BBS2-related_disorder": 1,
    "BBS2-related_ciliopathy|not_provided|Bardet-Biedl_syndrome": 1,
    "not_specified|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Bardet-biedl_syndrome_1/2|_digenic|Bardet-Biedl_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome_2|BBS2-related_disorder|not_provided|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|not_provided|Inborn_genetic_diseases|BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome|not_specified|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_1|not_provided|Bardet-Biedl_syndrome_2|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_2|Inborn_genetic_diseases|Retinitis_pigmentosa_74|BBS2-related_disorder|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome|Retinitis_pigmentosa_74": 1,
    "Inborn_genetic_diseases|BBS2-related_disorder|Retinal_dystrophy|Bardet-Biedl_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|BBS2-related_disorder|Bardet-Biedl_syndrome|Bardet-biedl_syndrome_1/2|_digenic|Retinitis_pigmentosa": 1,
    "Bardet-Biedl_syndrome|BBS2-related_disorder|not_specified|Bardet-Biedl_syndrome_2": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74|Retinal_dystrophy|not_provided": 1,
    "BBS2-related_ciliopathy|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|Bardet-Biedl_syndrome": 1,
    "BARDET-BIEDL_SYNDROME_2/6|_DIGENIC|Bardet-Biedl_syndrome": 1,
    "Retinitis_pigmentosa_74|Retinal_dystrophy|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_2|not_specified": 1,
    "Bardet-Biedl_syndrome_2|BBS2-related_disorder|Inborn_genetic_diseases|not_specified|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_2": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_2": 1,
    "BBS2-related_disorder|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|not_provided|Retinitis_pigmentosa_74": 1,
    "BBS2-related_disorder|Retinitis_pigmentosa|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_2|Retinitis_pigmentosa_74": 1,
    "Bardet-Biedl_syndrome_2|Retinal_dystrophy|BBS2-related_disorder": 1,
    "Retinal_disorders|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|BARDET-BIEDL_SYNDROME_2/6|_DIGENIC|Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|BBS2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_74|Bardet-Biedl_syndrome_2|not_specified": 1,
    "not_specified|Retinitis_pigmentosa_74|not_provided|Bardet-Biedl_syndrome_2": 1,
    "MT1X-related_disorder": 1,
    "Nephrotic_syndrome|_type_12": 21,
    "NUP93-related_disorder|not_provided": 6,
    "Nephrotic_syndrome|_type_12|not_provided": 4,
    "not_provided|Nephrotic_syndrome|_type_12": 7,
    "not_provided|NUP93-related_disorder": 5,
    "NUP93-related_disorder": 16,
    "not_provided|NUP93-related_disorder|Inborn_genetic_diseases": 1,
    "NUP93-related_disorder|Nephrotic_syndrome|_type_12|Nephrotic_syndrome|not_provided": 1,
    "not_provided|not_specified|NUP93-related_disorder": 1,
    "NUP93-related_disorder|Nephrotic_syndrome|_type_12|not_provided": 1,
    "Nephrotic_syndrome|Nephrotic_syndrome|_type_12|not_provided": 1,
    "Nephrotic_syndrome|_type_12|Nephrotic_syndrome": 1,
    "NUP93-related_disorder|not_provided|Nephrotic_syndrome|_type_12": 1,
    "Nephrotic_syndrome|_type_12|not_provided|Nephrotic_syndrome": 1,
    "Familial_hypokalemia-hypomagnesemia|Bartter_syndrome|not_provided": 2,
    "Familial_hypokalemia-hypomagnesemia|not_provided": 124,
    "not_provided|not_specified|Familial_hypokalemia-hypomagnesemia": 2,
    "Inborn_genetic_diseases|not_provided|Familial_hypokalemia-hypomagnesemia": 5,
    "not_provided|Familial_hypokalemia-hypomagnesemia": 161,
    "Inborn_genetic_diseases|Familial_hypokalemia-hypomagnesemia|not_provided": 4,
    "Familial_hypokalemia-hypomagnesemia|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|Familial_hypokalemia-hypomagnesemia|not_provided": 6,
    "Familial_hypokalemia-hypomagnesemia|not_provided|SLC12A3-related_disorder": 3,
    "Familial_hypokalemia-hypomagnesemia|Inborn_genetic_diseases": 14,
    "not_provided|Familial_hypokalemia-hypomagnesemia|Inborn_genetic_diseases": 4,
    "not_provided|Inborn_genetic_diseases|Familial_hypokalemia-hypomagnesemia": 6,
    "Familial_hypokalemia-hypomagnesemia|not_provided|Inborn_genetic_diseases": 6,
    "not_specified|Familial_hypokalemia-hypomagnesemia|Inborn_genetic_diseases|SLC12A3-related_disorder|not_provided": 1,
    "Familial_hypokalemia-hypomagnesemia|not_specified|not_provided": 8,
    "SLC12A3-related_disorder|not_specified|Hypokalemia": 1,
    "SLC12A3-related_disorder|not_provided": 4,
    "Familial_hypokalemia-hypomagnesemia|not_specified": 2,
    "Familial_hypokalemia-hypomagnesemia|not_provided|Muscle_weakness|Myalgia|Hypokalemia|Hypermagnesemia": 1,
    "Familial_hypokalemia-hypomagnesemia|Bartter_syndrome|not_provided|SLC12A3-related_disorder": 1,
    "SLC12A3-related_disorder": 7,
    "Inborn_genetic_diseases|not_provided|SLC12A3-related_disorder|Familial_hypokalemia-hypomagnesemia": 1,
    "Familial_hypokalemia-hypomagnesemia|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Familial_hypokalemia-hypomagnesemia": 1,
    "SLC12A3-related_disorder|not_specified|not_provided|Familial_hypokalemia-hypomagnesemia": 1,
    "SLC12A3-related_disorder|not_provided|Familial_hypokalemia-hypomagnesemia": 3,
    "not_provided|Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder": 6,
    "Familial_hypokalemia-hypomagnesemia|not_specified|Inborn_genetic_diseases|SLC12A3-related_disorder|not_provided": 1,
    "Familial_hypokalemia-hypomagnesemia|not_provided|not_specified": 5,
    "Renal_tubular_acidosis|not_provided|Familial_hypokalemia-hypomagnesemia": 1,
    "Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder": 1,
    "not_provided|SLC12A3-related_disorder": 3,
    "Familial_hypokalemia-hypomagnesemia|not_specified|SLC12A3-related_disorder|not_provided": 1,
    "not_specified|Familial_hypokalemia-hypomagnesemia": 1,
    "not_provided|Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder|not_specified": 1,
    "not_provided|Bartter_syndrome|Familial_hypokalemia-hypomagnesemia": 2,
    "Familial_aortopathy|SLC12A3-related_disorder|Familial_hypokalemia-hypomagnesemia|Bartter_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Bartter_syndrome|Familial_hypokalemia-hypomagnesemia|not_provided": 3,
    "Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder|not_provided": 3,
    "not_provided|Familial_hypokalemia-hypomagnesemia|not_specified": 6,
    "Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "SLC12A3-related_disorder|Familial_hypokalemia-hypomagnesemia|not_provided": 1,
    "Familial_hypokalemia-hypomagnesemia|not_provided|not_specified|SLC12A3-related_disorder": 1,
    "not_provided|Familial_hypokalemia-hypomagnesemia|Renal_tubulopathies": 1,
    "Inborn_genetic_diseases|not_provided|Familial_hypokalemia-hypomagnesemia|Bartter_syndrome": 1,
    "not_provided|SLC12A3-related_disorder|Familial_hypokalemia-hypomagnesemia": 2,
    "not_specified|not_provided|Familial_hypokalemia-hypomagnesemia": 3,
    "Familial_hypokalemia-hypomagnesemia|not_specified|not_provided|Inborn_genetic_diseases|SLC12A3-related_disorder": 1,
    "SLC12A3-related_disorder|Familial_hypokalemia-hypomagnesemia|Bartter_syndrome|Inherited_renal_tubular_disease|not_provided|Muscle_weakness|Hypokalemia|Hypermagnesemia|Myalgia": 1,
    "not_specified|Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder": 1,
    "SLC12A3-related_disorder|not_provided|Inborn_genetic_diseases|Familial_hypokalemia-hypomagnesemia": 1,
    "Renal_tubular_acidosis|not_specified": 1,
    "Inborn_genetic_diseases|Familial_hypokalemia-hypomagnesemia": 1,
    "not_provided|Familial_hypokalemia-hypomagnesemia|SLC12A3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hypokalemia-hypomagnesemia|Bartter_syndrome": 1,
    "SLC12A3-related_disorder|not_provided|Familial_hypokalemia-hypomagnesemia|not_specified": 1,
    "not_provided|Familial_hypokalemia-hypomagnesemia|Bartter_syndrome|Inborn_genetic_diseases": 1,
    "High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_10": 1,
    "Hyperalphalipoproteinemia_1|not_provided": 17,
    "Hyperalphalipoproteinemia_1|not_provided|not_specified": 2,
    "CETP-related_disorder|Hyperalphalipoproteinemia_1|not_provided": 2,
    "Hyperalphalipoproteinemia_1|not_specified|not_provided": 3,
    "Hyperalphalipoproteinemia_1": 17,
    "not_provided|Hyperalphalipoproteinemia_1": 13,
    "not_provided|Hyperalphalipoproteinemia_1|CETP-related_disorder": 4,
    "CETP-related_disorder": 2,
    "not_provided|Hyperalphalipoproteinemia_1|not_specified": 1,
    "not_provided|CETP-related_disorder": 1,
    "Hyperalphalipoproteinemia_1|not_specified": 1,
    "Cholesterol-ester_transfer_protein_deficiency": 2,
    "not_specified|Hyperalphalipoproteinemia_1|not_provided": 2,
    "Hyperalphalipoproteinemia_1|not_provided|CETP-related_disorder": 1,
    "not_specified|Abnormal_circulating_lipid_concentration": 1,
    "not_specified|Hyperalphalipoproteinemia_1": 1,
    "Hyperalphalipoproteinemia_1|CETP-related_disorder|not_provided": 2,
    "CETP-related_disorder|not_provided": 1,
    "Coronary_artery_disorder|not_provided|High_density_lipoprotein_cholesterol_level_quantitative_trait_locus_10|Hyperalphalipoproteinemia_1|not_specified": 1,
    "Progressive_spondyloepimetaphyseal_dysplasia-short_stature-short_fourth_metatarsals-intellectual_disability_syndrome|not_provided": 2,
    "Progressive_spondyloepimetaphyseal_dysplasia-short_stature-short_fourth_metatarsals-intellectual_disability_syndrome": 10,
    "RSPRY1-related_disorder|not_provided": 1,
    "not_provided|RSPRY1-related_disorder": 2,
    "Retinitis_pigmentosa_with_or_without_situs_inversus": 2,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_with_or_without_situs_inversus": 1,
    "not_provided|Retinitis_pigmentosa_with_or_without_situs_inversus": 2,
    "Retinitis_pigmentosa_with_or_without_situs_inversus|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_with_or_without_situs_inversus|ARL2BP-related_disorder|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_with_or_without_situs_inversus|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_with_or_without_situs_inversus|not_provided|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_with_or_without_situs_inversus|not_provided": 1,
    "ARL2BP-related_disorder|not_provided": 1,
    "Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome": 26,
    "COQ9-related_disorder": 4,
    "Inborn_genetic_diseases|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome": 1,
    "Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome": 9,
    "not_specified|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_provided": 2,
    "COQ9-related_disorder|not_provided|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome": 1,
    "Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_specified": 1,
    "Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_provided": 8,
    "Inborn_genetic_diseases|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 2,
    "not_provided|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|COQ9-related_disorder": 1,
    "Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|COQ9-related_disorder|not_provided": 1,
    "not_provided|COQ9-related_disorder": 4,
    "not_provided|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_specified": 2,
    "COQ9-related_disorder|not_provided": 2,
    "not_specified|COQ9-related_disorder": 1,
    "COQ9-related_disorder|not_specified|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_provided": 1,
    "COQ9-related_disorder|not_provided|Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|Leigh_syndrome": 1,
    "Encephalopathy-hypertrophic_cardiomyopathy-renal_tubular_disease_syndrome|not_provided|not_specified": 1,
    "Deafness|Infertility_disorder": 1,
    "Bilateral_frontoparietal_polymicrogyria": 114,
    "Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|not_provided": 1,
    "Bilateral_frontoparietal_polymicrogyria|not_provided": 47,
    "Bilateral_frontoparietal_polymicrogyria|not_specified": 2,
    "not_provided|Bilateral_frontoparietal_polymicrogyria|Inborn_genetic_diseases": 4,
    "Bilateral_frontoparietal_polymicrogyria|not_provided|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive": 4,
    "not_provided|ADGRG1-related_disorder|Congenital_myopathy": 1,
    "not_provided|Bilateral_frontoparietal_polymicrogyria": 40,
    "Bilateral_frontoparietal_polymicrogyria|Inborn_genetic_diseases|not_provided": 5,
    "Abnormality_of_the_nervous_system|not_provided|Inborn_genetic_diseases|Bilateral_frontoparietal_polymicrogyria": 1,
    "not_provided|Bilateral_frontoparietal_polymicrogyria|not_specified": 4,
    "Bilateral_frontoparietal_polymicrogyria|not_specified|ADGRG1-related_disorder|not_provided": 1,
    "not_provided|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|Bilateral_frontoparietal_polymicrogyria": 1,
    "not_provided|Bilateral_frontoparietal_polymicrogyria|ADGRG1-related_disorder": 2,
    "not_provided|Bilateral_frontoparietal_polymicrogyria|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive": 2,
    "ADGRG1-related_disorder|not_provided": 6,
    "Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|Bilateral_frontoparietal_polymicrogyria": 6,
    "Inborn_genetic_diseases|not_provided|Bilateral_frontoparietal_polymicrogyria": 3,
    "not_specified|Bilateral_frontoparietal_polymicrogyria": 1,
    "Inborn_genetic_diseases|Bilateral_frontoparietal_polymicrogyria": 3,
    "Bilateral_frontoparietal_polymicrogyria|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|not_provided": 4,
    "Bilateral_frontoparietal_polymicrogyria|not_provided|not_specified|ADGRG1-related_disorder": 3,
    "not_provided|Bilateral_frontoparietal_polymicrogyria|ADGRG1-related_disorder|not_specified": 1,
    "Bilateral_frontoparietal_polymicrogyria|not_specified|not_provided": 7,
    "ADGRG1-related_disorder": 2,
    "ADGRG1-related_disorder|not_specified|not_provided|Bilateral_frontoparietal_polymicrogyria": 1,
    "not_provided|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive": 1,
    "Bilateral_frontoparietal_polymicrogyria|not_provided|ADGRG1-related_disorder": 1,
    "Inborn_genetic_diseases|Bilateral_frontoparietal_polymicrogyria|not_provided": 1,
    "Bilateral_frontoparietal_polymicrogyria|Inborn_genetic_diseases": 1,
    "ADGRG1-related_disorder|not_provided|Bilateral_frontoparietal_polymicrogyria": 1,
    "not_provided|Inborn_genetic_diseases|Bilateral_frontoparietal_polymicrogyria": 1,
    "not_specified|not_provided|Bilateral_frontoparietal_polymicrogyria|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive": 1,
    "ADGRG1-related_disorder|Bilateral_frontoparietal_polymicrogyria|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|not_specified|not_provided": 1,
    "Bilateral_frontoparietal_polymicrogyria|not_provided|not_specified": 3,
    "Bilateral_frontoparietal_polymicrogyria|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive": 2,
    "not_provided|not_specified|Bilateral_frontoparietal_polymicrogyria": 3,
    "not_provided|ADGRG1-related_disorder": 2,
    "Bilateral_frontoparietal_polymicrogyria|ADGRG1-related_disorder|not_specified|not_provided": 2,
    "Bilateral_frontoparietal_polymicrogyria|ADGRG1-related_disorder|not_provided": 1,
    "Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|Bilateral_frontoparietal_polymicrogyria|not_provided": 1,
    "Bilateral_frontoparietal_polymicrogyria|Global_developmental_delay|Macrogyria|Visual_impairment|Generalized-onset_seizure|Intellectual_disability|_moderate|Strabismus|Generalized_weakness_of_limb_muscles": 1,
    "not_specified|Polymicrogyria|_bilateral_perisylvian|_autosomal_recessive|Bilateral_frontoparietal_polymicrogyria": 1,
    "Bilateral_frontoparietal_polymicrogyria|not_specified|not_provided|ADGRG1-related_disorder": 1,
    "not_specified|not_provided|Bilateral_frontoparietal_polymicrogyria": 1,
    "Lissencephaly_6_with_microcephaly": 14,
    "not_provided|KATNB1-related_disorder": 9,
    "KATNB1-related_disorder|not_provided": 5,
    "not_provided|Lissencephaly_6_with_microcephaly": 2,
    "not_provided|KATNB1-related_disorder|not_specified": 1,
    "KATNB1-related_disorder": 7,
    "not_specified|KATNB1-related_disorder|not_provided": 1,
    "Lissencephaly_6_with_microcephaly|not_provided": 3,
    "KATNB1-related_disorder|not_specified|not_provided": 1,
    "KATNB1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|KATNB1-related_disorder": 2,
    "KATNB1-related_disorder|Lissencephaly_6_with_microcephaly": 1,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_6_with_microcephaly": 1,
    "CNGB1-related_retinopathy|Retinal_dystrophy": 1,
    "CNGB1-related_disorder|not_provided": 7,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa_45": 1,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|not_provided|CNGB1-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_45": 4,
    "Retinitis_pigmentosa_45": 43,
    "Retinitis_pigmentosa|not_specified|not_provided|Retinitis_pigmentosa_45": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|CNGB1-related_retinopathy": 1,
    "CNGB1-related_retinopathy": 3,
    "Retinitis_pigmentosa|not_provided|CNGB1-related_disorder": 4,
    "Retinitis_pigmentosa_45|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_45|not_provided": 3,
    "Retinitis_pigmentosa|CNGB1-related_disorder|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_45": 1,
    "CNGB1-related_retinopathy|CNGB1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_45": 17,
    "Retinitis_pigmentosa_45|not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa": 1,
    "CNGB1-related_disorder|CNGB1-related_retinopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Autosomal_recessive_retinitis_pigmentosa|Retinitis_pigmentosa_45": 1,
    "Retinitis_pigmentosa_45|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_45|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_45": 1,
    "Retinitis_pigmentosa_45|Retinal_dystrophy|Retinitis_pigmentosa|CNGB1-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_45|not_provided|CNGB1-related_retinopathy": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|CNGB1-related_retinopathy|not_specified": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa": 2,
    "not_specified|Retinitis_pigmentosa_45|Retinitis_pigmentosa|not_provided": 1,
    "not_specified|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 2,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_45": 3,
    "Retinitis_pigmentosa_45|not_provided": 16,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_45|not_specified": 1,
    "not_provided|CNGB1-related_disorder|not_specified": 1,
    "Retinitis_pigmentosa_45|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_45|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|CNGB1-related_retinopathy|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|CNGB1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Retinitis_pigmentosa_45|Retinitis_pigmentosa|not_provided": 2,
    "Retinitis_pigmentosa|not_specified|CNGB1-related_disorder|not_provided|Retinitis_pigmentosa_45": 1,
    "not_provided|Retinal_dystrophy|not_specified|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_45|Autosomal_recessive_retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_45|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_45": 2,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_45|not_provided|not_specified": 2,
    "Retinitis_pigmentosa|not_provided|CNGB1-related_retinopathy|Retinal_dystrophy|CNGB1-related_disorder": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_45": 2,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_45|Retinal_dystrophy": 1,
    "not_provided|CNGB1-related_disorder": 3,
    "not_provided|CNGB1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Retinitis_pigmentosa_45|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_45|not_provided": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_45": 2,
    "Retinitis_pigmentosa_49|Retinitis_pigmentosa_45|Retinitis_pigmentosa|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|not_specified|Retinitis_pigmentosa|Retinitis_pigmentosa_45": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|not_provided|CNGB1-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_45": 1,
    "CNGB1-related_disorder|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa_45|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_45|Retinitis_pigmentosa|not_specified": 1,
    "not_specified|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa_45|not_provided": 1,
    "CNGB1-related_disorder|not_provided|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_45": 2,
    "not_provided|Retinitis_pigmentosa|CNGB1-related_disorder|Inborn_genetic_diseases|Optic_atrophy": 1,
    "not_specified|Retinitis_pigmentosa_45|CNGB1-related_disorder|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_45|CNGB1-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "not_provided|CNGB1-related_retinopathy": 1,
    "Retinitis_pigmentosa_45|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|not_specified": 1,
    "Retinitis_pigmentosa_45|not_provided|Retinal_dystrophy|Retinitis_pigmentosa|not_specified": 1,
    "CNGB1-related_disorder": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_45|CNGB1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|CNGB1-related_disorder": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_45|CNGB1-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|CNGB1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_45": 2,
    "Poikiloderma_with_neutropenia|not_provided": 5,
    "Poikiloderma_with_neutropenia": 18,
    "not_provided|Poikiloderma_with_neutropenia|not_specified": 1,
    "Poikiloderma_with_neutropenia|USB1-related_disorder|not_provided": 1,
    "Poikiloderma_with_neutropenia|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|USB1-related_disorder": 2,
    "not_provided|Poikiloderma_with_neutropenia": 12,
    "Poikiloderma_with_neutropenia|Inborn_genetic_diseases|not_provided": 4,
    "USB1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Poikiloderma_with_neutropenia": 3,
    "not_provided|Poikiloderma_with_neutropenia|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|USB1-related_disorder": 1,
    "USB1-related_disorder": 1,
    "not_specified|Poikiloderma_with_neutropenia|not_provided": 1,
    "not_provided|USB1-related_disorder|Inborn_genetic_diseases": 1,
    "Poikiloderma_with_neutropenia|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Poikiloderma_with_neutropenia|not_specified": 1,
    "Inborn_genetic_diseases|Poikiloderma_with_neutropenia": 1,
    "CSNK2A2-related_disorder": 1,
    "GINS3-related_disorder": 1,
    "NDRG4-related_disorder": 6,
    "NDRG4-related_disorder|not_provided": 2,
    "Vissers-Bodmer_syndrome": 35,
    "not_provided|CNOT1-related_disorder": 8,
    "CNOT1-related_disorder": 17,
    "Vissers-Bodmer_syndrome|Holoprosencephaly_12_with_or_without_pancreatic_agenesis|not_provided": 3,
    "CNOT1-related_disorder|not_provided": 11,
    "Holoprosencephaly_12_with_or_without_pancreatic_agenesis": 6,
    "CNOT1-related_disorder|Vissers-Bodmer_syndrome|Holoprosencephaly_12_with_or_without_pancreatic_agenesis|not_provided": 2,
    "Holoprosencephaly_12_with_or_without_pancreatic_agenesis|Vissers-Bodmer_syndrome": 5,
    "Preterm_intraventricular_hemorrhage": 1,
    "Inborn_genetic_diseases|CNOT1-related_disorder|not_provided": 1,
    "Holoprosencephaly_12_with_or_without_pancreatic_agenesis|CNOT1-related_disorder|not_provided": 1,
    "not_provided|Holoprosencephaly_12_with_or_without_pancreatic_agenesis": 2,
    "not_provided|Vissers-Bodmer_syndrome": 1,
    "not_provided|Holoprosencephaly_12_with_or_without_pancreatic_agenesis|Vissers-Bodmer_syndrome": 1,
    "Vissers-Bodmer_syndrome|Holoprosencephaly_12_with_or_without_pancreatic_agenesis": 4,
    "Alopecia-intellectual_disability_syndrome_4": 16,
    "CNOT1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CNOT1-related_disorder": 1,
    "Vissers-Bodmer_syndrome|Inborn_genetic_diseases": 1,
    "Vissers-Bodmer_syndrome|Holoprosencephaly_sequence|Holoprosencephaly_12_with_or_without_pancreatic_agenesis": 1,
    "not_provided|Inborn_genetic_diseases|CNOT1-related_disorder": 1,
    "Nuerodevelopment_disorder": 1,
    "Holoprosencephaly_12_with_or_without_pancreatic_agenesis|Inborn_genetic_diseases|not_provided": 1,
    "Vissers-Bodmer_syndrome|not_provided": 1,
    "See_cases|Vissers-Bodmer_syndrome": 1,
    "CNOT1-related_disorder|Inborn_genetic_diseases": 1,
    "See_cases|Vissers-Bodmer_syndrome|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_82": 4,
    "Developmental_and_epileptic_encephalopathy|_82|Developmental_and_epileptic_encephalopathy": 4,
    "GOT2-related_disorder|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_82|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_82|not_specified": 2,
    "not_provided|GOT2-related_disorder": 1,
    "not_provided|GOT2-related_disorder|Developmental_and_epileptic_encephalopathy|_82": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_82": 1,
    "Developmental_and_epileptic_encephalopathy|_82|not_specified|not_provided": 1,
    "CDH11-related_disorder": 6,
    "Teebi_hypertelorism_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|CDH11-related_disorder": 1,
    "Elsahy-Waters_syndrome": 9,
    "Teebi_hypertelorism_syndrome_2": 8,
    "not_provided|Elsahy-Waters_syndrome": 8,
    "Elsahy-Waters_syndrome|Teebi_hypertelorism_syndrome_2": 1,
    "CDH5-related_condition": 1,
    "Spinocerebellar_ataxia_type_31": 2,
    "BEAN1-related_disorder|not_provided": 1,
    "BEAN1-related_disorder": 6,
    "not_provided|BEAN1-related_disorder": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 9,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 69,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided": 4,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_specified|not_provided": 2,
    "not_provided|not_specified|Mitochondrial_disease": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Inborn_mitochondrial_myopathy|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_specified": 1,
    "Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 3,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 2,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided|Mitochondrial_disease": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_provided|Mitochondrial_disease": 2,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided": 2,
    "Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_provided": 2,
    "Inborn_genetic_diseases|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Mitochondrial_DNA_depletion_syndrome|not_provided": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_provided|Mitochondrial_disease": 1,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 2,
    "Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_disease": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Mitochondrial_disease": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_disease": 1,
    "not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 2,
    "TK2-related_disorder|not_provided": 5,
    "Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided|TK2-related_disorder|Mitochondrial_DNA_depletion_syndrome": 1,
    "Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "not_provided|TK2-related_disorder": 3,
    "Mitochondrial_disease|not_provided|Mitochondrial_DNA_depletion_syndrome": 2,
    "not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Mitochondrial_DNA_depletion_syndrome": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_disease|not_provided": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Mitochondrial_disease|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Mitochondrial_DNA_depletion_syndrome|Mitochondrial_disease": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|not_provided": 1,
    "Mitochondrial_disease|not_specified": 4,
    "not_specified|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Mitochondrial_disease": 2,
    "TK2-related_disorder|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "Mitochondrial_DNA_depletion_syndrome|Mitochondrial_disease|not_provided|Abnormality_of_the_musculature": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Mitochondrial_DNA_depletion_syndrome|not_provided|Mitochondrial_disease": 1,
    "TK2-related_disorder|not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "Mitochondrial_disease|not_specified|not_provided": 2,
    "Mitochondrial_disease|Myopathy|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided|not_specified": 1,
    "TK2-related_disorder|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_disease|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided|Mitochondrial_DNA_depletion_syndrome_2|_myopathic_form|Mitochondrial_disease": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_specified": 1,
    "not_specified|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided": 1,
    "Mitochondrial_disease|not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|Mitochondrial_disease": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided|not_specified": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|TK2-related_disorder": 1,
    "TK2-related_disorder|not_specified|not_provided|Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form": 1,
    "Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_provided": 1,
    "Mitochondrial_disease|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3": 1,
    "Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome|_myopathic_form|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_3|not_specified": 1,
    "Spermatogenic_failure_60": 2,
    "Non-obstructive_azoospermia|Spermatogenic_failure_60": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_ischiopubic_hypoplasia": 5,
    "not_provided|not_specified|Neurodevelopmental_disorder_with_dysmorphic_facies_and_ischiopubic_hypoplasia": 1,
    "Cleidocranial_dysplasia_2": 2,
    "CBFB-related_disorder": 4,
    "Cleidocranial_dysplasia_2|not_provided": 2,
    "Acute_myeloid_leukemia|Cleidocranial_dysplasia_2": 1,
    "TRADD-related_disorder": 2,
    "not_provided|Cataract_5_multiple_types": 9,
    "Cataract_5_multiple_types|not_specified": 1,
    "Cataract_5_multiple_types": 72,
    "FBXL8-related_disorder": 1,
    "HSF4-related_disorder": 9,
    "not_provided|Cataract_5_multiple_types|HSF4-related_disorder": 2,
    "Inborn_genetic_diseases|Cataract_5_multiple_types": 10,
    "Cataract_5_multiple_types|not_provided": 3,
    "not_provided|Cataract_5_multiple_types|not_specified": 1,
    "Cataract_5_multiple_types|Inborn_genetic_diseases": 2,
    "HSF4-related_disorder|Cataract_5_multiple_types": 3,
    "HSF4-related_disorder|Cataract_5_multiple_types|not_provided": 1,
    "Cataract_5_multiple_types|HSF4-related_disorder": 2,
    "not_provided|HSF4-related_disorder|Cataract_5_multiple_types": 1,
    "Cataract_5_multiple_types|Inborn_genetic_diseases|HSF4-related_disorder|not_provided": 1,
    "not_provided|Cataract_5_multiple_types|Inborn_genetic_diseases": 1,
    "HSF4-related_disorder|Inborn_genetic_diseases": 1,
    "NOL3-related_disorder": 8,
    "Myoclonus|_familial|_1": 2,
    "Myoclonus|_familial": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|not_provided": 3,
    "PLEKHG4-related_disorder": 1,
    "Inborn_genetic_diseases|Apparent_mineralocorticoid_excess": 3,
    "Apparent_mineralocorticoid_excess": 60,
    "Apparent_mineralocorticoid_excess|Inborn_genetic_diseases|not_provided": 1,
    "HSD11B2-related_disorder|Apparent_mineralocorticoid_excess|not_specified|not_provided": 1,
    "Apparent_mineralocorticoid_excess|_mild|Apparent_mineralocorticoid_excess": 1,
    "Apparent_mineralocorticoid_excess|Inborn_genetic_diseases": 2,
    "Apparent_mineralocorticoid_excess|not_specified": 1,
    "Apparent_mineralocorticoid_excess|not_provided": 6,
    "HSD11B2-related_disorder|Apparent_mineralocorticoid_excess|not_provided": 1,
    "not_provided|Apparent_mineralocorticoid_excess": 9,
    "HSD11B2-related_disorder|not_provided": 1,
    "HSD11B2-related_disorder": 1,
    "Apparent_mineralocorticoid_excess|_mild": 1,
    "not_provided|Apparent_mineralocorticoid_excess|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Apparent_mineralocorticoid_excess|not_provided": 1,
    "not_specified|Apparent_mineralocorticoid_excess": 2,
    "Inborn_genetic_diseases|Apparent_mineralocorticoid_excess|not_provided|not_specified": 1,
    "AGRP-related_condition|Inherited_obesity|Obesity|_late-onset|Leanness|_inherited": 1,
    "CTCF-related_disorder": 11,
    "Syndromic_X-linked_intellectual_disability_Shashi_type": 10,
    "CTCF-related_disorder|not_provided": 2,
    "not_provided|CTCF-related_disorder": 2,
    "not_provided|Desmoplastic/nodular_medulloblastoma": 1,
    "Intellectual_disability|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|not_provided": 1,
    "CTCF-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CTCF-related_disorder|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome": 2,
    "Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|not_specified": 1,
    "not_provided|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|Inborn_genetic_diseases": 1,
    "CTCF-related_neurodevelopmental_disorder|not_provided|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome": 1,
    "Inborn_genetic_diseases|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome": 1,
    "CTCF-related_syndromic_intellectual_disability": 1,
    "CTCF-related_syndromic_intellectual_disability|Inborn_genetic_diseases|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|not_provided|Intellectual_disability": 1,
    "not_provided|CTCF-related_disorder|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|CTCF-related_disorder": 1,
    "not_specified|not_provided|CTCF-related_disorder": 1,
    "CTCF-related_disorder|Inborn_genetic_diseases|Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|not_specified|not_provided": 1,
    "Intellectual_disability-feeding_difficulties-developmental_delay-microcephaly_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "CTCF-related_disorder|Inborn_genetic_diseases": 1,
    "CTCF-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|CTCF-related_disorder": 1,
    "Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency": 18,
    "CARMIL2-related_disorder|not_provided": 13,
    "not_provided|Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency": 8,
    "not_provided|CARMIL2-related_disorder": 19,
    "Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency|not_provided": 12,
    "Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency|Combined_immunodeficiency": 2,
    "CARMIL2-related_disorder": 4,
    "Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency|CARMIL2-related_disorder": 1,
    "Combined_immunodeficiency|Chronic_colitis|Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency": 1,
    "not_specified|not_provided|Severe_combined_immunodeficiency_due_to_CARMIL2_deficiency": 1,
    "CARMIL2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6": 273,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|Inborn_genetic_diseases": 126,
    "not_specified|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6": 144,
    "ACD-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|not_specified|not_provided": 1,
    "ACD-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_6|Inborn_genetic_diseases": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_6|not_specified": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_6|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|not_specified": 6,
    "Dyskeratosis_congenita|_autosomal_dominant_6|Inborn_genetic_diseases|not_specified": 2,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_7|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "not_provided|not_specified|Dyskeratosis_congenita|_autosomal_dominant_6": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_6": 6,
    "ACD-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_6": 3,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_dominant_6": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_6|not_provided": 2,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|not_provided": 3,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_6|Inborn_genetic_diseases": 4,
    "not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6": 3,
    "Dyskeratosis_congenita|_autosomal_dominant_6|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|ACD-related_disorder": 2,
    "not_specified|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6": 6,
    "Dyskeratosis_congenita|_autosomal_dominant_6|not_specified": 8,
    "Dyskeratosis_congenita|_autosomal_dominant_6|not_specified|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita|_autosomal_dominant_6": 4,
    "not_provided|not_specified|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|ACD-related_disorder|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|ACD-related_disorder": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_6": 4,
    "Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita|_autosomal_dominant_6|not_provided": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_6|not_provided|Inborn_genetic_diseases|ACD-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|ACD-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|ACD-related_short_telomere_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ACD-related_disorder|not_provided|not_specified|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "ACD-related_disorder|Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_dominant_6|not_provided": 2,
    "Long_telomere_syndrome|Dyskeratosis_congenita|_autosomal_dominant_6|not_specified|not_provided": 1,
    "ACD-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|not_specified": 2,
    "Long_telomere_syndrome|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|Dyskeratosis_congenita|_autosomal_recessive_7": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|not_specified|not_provided": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|_autosomal_dominant_6|ACD-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ACD-related_disorder": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_dominant_6|not_provided|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_6|Inborn_genetic_diseases|ACD-related_disorder": 1,
    "Inborn_genetic_diseases|ACD-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_6": 1,
    "PARD6A-related_disorder": 4,
    "CENPT-related_disorder": 15,
    "not_provided|Short_stature_and_microcephaly_with_genital_anomalies": 2,
    "Short_stature_and_microcephaly_with_genital_anomalies": 1,
    "not_provided|CENPT-related_disorder": 2,
    "Short_stature_and_microcephaly_with_genital_anomalies|not_provided|CENPT-related_disorder": 1,
    "THAP11-related_disorder|not_provided": 11,
    "THAP11-related_disorder|not_specified|not_provided": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|Methylmalonic_aciduria_and_homocystinuria|_cb1L_type|Disorders_of_Intracellular_Cobalamin_Metabolism": 1,
    "not_provided|THAP11-related_disorder": 3,
    "Cholestasis|_progressive_familial_intrahepatic|_13": 4,
    "Proteasome-associated_autoinflammatory_syndrome_5|not_specified": 1,
    "Proteasome-associated_autoinflammatory_syndrome_5": 7,
    "Immunodeficiency_121_with_autoinflammation": 3,
    "PSMB10-related_disorder": 2,
    "Norum_disease|Fish-eye_disease": 35,
    "not_provided|Fish-eye_disease|Norum_disease|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Fish-eye_disease|Norum_disease|not_provided": 1,
    "LCAT-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Norum_disease|Fish-eye_disease|LCAT_deficiency": 1,
    "LCAT_deficiency|Cardiovascular_phenotype": 1,
    "not_provided|LCAT-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|LCAT_deficiency": 1,
    "Fish-eye_disease|Norum_disease": 2,
    "Cardiovascular_phenotype|Fish-eye_disease|Norum_disease": 2,
    "not_provided|Norum_disease|Fish-eye_disease": 1,
    "LCAT_deficiency|Fish-eye_disease|Norum_disease|not_provided": 1,
    "not_provided|Fish-eye_disease|Norum_disease": 2,
    "not_provided|Norum_disease|Fish-eye_disease|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|LCAT_deficiency": 6,
    "Fish-eye_disease": 3,
    "Norum_disease": 4,
    "Cardiovascular_phenotype|Norum_disease|Fish-eye_disease": 2,
    "not_provided|Cardiovascular_phenotype|LCAT-related_disorder": 1,
    "Norum_disease|Fish-eye_disease|Cardiovascular_phenotype": 2,
    "not_provided|LCAT_deficiency": 1,
    "Cardiovascular_phenotype|LCAT_deficiency|LCAT-related_disorder|Norum_disease|Fish-eye_disease|not_provided": 1,
    "not_provided|LCAT_deficiency|Cardiovascular_phenotype": 1,
    "Fish-eye_disease|Norum_disease|Cardiovascular_phenotype": 2,
    "not_provided|LCAT-related_disorder": 2,
    "Norum_disease|Fish-eye_disease|LCAT_deficiency": 2,
    "LCAT_deficiency|not_provided": 2,
    "Fish-eye_disease|Norum_disease|not_provided": 3,
    "Cardiovascular_phenotype|LCAT_deficiency": 1,
    "Fish-eye_disease|not_provided|Norum_disease|LCAT-related_disorder": 1,
    "LCAT_deficiency|Fish-eye_disease|Norum_disease|Cardiovascular_phenotype|not_provided": 1,
    "LCAT_deficiency|Fish-eye_disease|Norum_disease": 1,
    "Norum_disease|Fish-eye_disease|not_provided|Cardiovascular_phenotype|LCAT_deficiency": 1,
    "LCAT_deficiency|not_provided|Fish-eye_disease|Norum_disease": 1,
    "Norum_disease|Fish-eye_disease|not_provided": 2,
    "Norum_disease|Fish-eye_disease|Cardiovascular_phenotype|not_provided": 1,
    "LCAT_deficiency|not_provided|Cardiovascular_phenotype": 1,
    "Fish-eye_disease|Norum_disease|Cardiovascular_phenotype|not_provided": 1,
    "ESRP2-related_disorder": 17,
    "not_provided|ESRP2-related_disorder": 2,
    "ESRP2-related_disorder|not_specified": 2,
    "SLC7A6-related_disorder": 5,
    "Epilepsy|_progressive_myoclonic|_12": 2,
    "not_specified|not_provided|Generalized_myoclonic_seizure|Epilepsy|_progressive_myoclonic|_12": 1,
    "Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome": 39,
    "PRMT7-related_disorder": 4,
    "not_provided|Acanthosis_nigricans|Obesity|Self-injurious_behavior|Renal_hypoplasia|Hepatic_steatosis|Abnormality_of_the_dentition|Abnormal_facial_shape|Lumbar_hyperlordosis|Hyperlipidemia|Short_stature|Short_metacarpal|Intellectual_disability|_severe|Brachydactyly|Skeletal_dysplasia|Insulin_resistance|Inborn_genetic_diseases|Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome": 1,
    "not_provided|not_specified|PRMT7-related_disorder": 1,
    "not_provided|Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome": 5,
    "Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome|not_provided": 8,
    "Inborn_genetic_diseases|Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome": 3,
    "not_provided|PRMT7-related_disorder": 7,
    "not_provided|Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_abnormality|not_provided|PRMT7-related_disorder|Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome": 1,
    "Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Acanthosis_nigricans|Obesity|Self-injurious_behavior|Renal_hypoplasia|Hepatic_steatosis|Abnormality_of_the_dentition|Abnormal_facial_shape|Lumbar_hyperlordosis|Hyperlipidemia|Short_stature|Short_metacarpal|Intellectual_disability|_severe|Brachydactyly|Skeletal_dysplasia|Insulin_resistance": 1,
    "not_provided|PRMT7-related_disorder|Short_stature-brachydactyly-obesity-global_developmental_delay_syndrome": 1,
    "not_provided|PRMT7-related_disorder|not_specified": 1,
    "EEM_syndrome": 49,
    "not_provided|EEM_syndrome": 18,
    "CDH3-related_disorder": 4,
    "Inborn_genetic_diseases|EEM_syndrome|not_provided": 3,
    "EEM_syndrome|not_provided": 23,
    "EEM_syndrome|CDH3-related_disorder|not_provided": 3,
    "not_provided|Retinal_dystrophy|Congenital_hypotrichosis_with_juvenile_macular_dystrophy": 1,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy|EEM_syndrome|not_provided": 2,
    "not_provided|Congenital_hypotrichosis_with_juvenile_macular_dystrophy|EEM_syndrome": 3,
    "CDH3-related_disorder|not_provided": 8,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy|Retinal_dystrophy|not_provided": 1,
    "not_provided|EEM_syndrome|Congenital_hypotrichosis_with_juvenile_macular_dystrophy": 1,
    "not_provided|CDH3-related_disorder": 6,
    "CDH3-related_disorder|Retinal_dystrophy": 1,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy|not_provided": 2,
    "Hypotrichosis_simplex": 1,
    "EEM_syndrome|Congenital_hypotrichosis_with_juvenile_macular_dystrophy|not_provided": 4,
    "not_provided|Hypotrichosis_with_juvenile_macular_dystrophy": 1,
    "CDH3-related_disorder|not_specified|not_provided|EEM_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|EEM_syndrome": 1,
    "EEM_syndrome|Congenital_hypotrichosis_with_juvenile_macular_dystrophy|Macular_dystrophy|not_provided": 1,
    "Hypotrichosis_with_juvenile_macular_dystrophy": 1,
    "not_provided|Hypotrichosis": 1,
    "Inborn_genetic_diseases|Congenital_hypotrichosis_with_juvenile_macular_dystrophy|EEM_syndrome": 1,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy|Hypotrichosis_with_juvenile_macular_dystrophy": 1,
    "not_provided|Congenital_hypotrichosis_with_juvenile_macular_dystrophy|Retinal_dystrophy": 1,
    "not_specified|not_provided|EEM_syndrome": 2,
    "EEM_syndrome|Inborn_genetic_diseases|Retinal_dystrophy|not_provided": 1,
    "EEM_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Retinal_dystrophy|EEM_syndrome|not_provided|not_specified|CDH3-related_disorder": 1,
    "EEM_syndrome|not_provided|CDH3-related_disorder": 1,
    "not_provided|EEM_syndrome|not_specified": 1,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy|not_provided|Retinal_dystrophy": 1,
    "CDH3-related_disorder|EEM_syndrome|not_provided": 2,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy": 2,
    "EEM_syndrome|Inborn_genetic_diseases|Congenital_hypotrichosis_with_juvenile_macular_dystrophy|not_provided": 1,
    "EEM_syndrome|Congenital_hypotrichosis_with_juvenile_macular_dystrophy": 2,
    "Congenital_hypotrichosis_with_juvenile_macular_dystrophy|EEM_syndrome|not_provided|not_specified": 1,
    "concomitant_exotropia|not_provided|Inborn_genetic_diseases": 1,
    "CDH3-related_disorder|EEM_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Prostate_cancer_susceptibility|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Prostate_cancer|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 10,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Prostate_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 4,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 19,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 37,
    "CDH1-related_disorder": 4,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 14,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 3,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|not_provided|Ovarian_cancer|Familial_cancer_of_breast|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 5,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 16,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 8,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|not_specified|Prostate_cancer|Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Blepharocheilodontic_syndrome_1|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|Familial_cancer_of_breast": 2,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Endometrial_carcinoma|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Ovarian_neoplasm|Prostate_cancer": 1,
    "Prostate_cancer|Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 20,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 35,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 24,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 18,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Gastric_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|not_provided|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 10,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 6,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Ovarian_cancer|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Familial_cancer_of_breast": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 7,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 13,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Familial_cancer_of_breast|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Prostate_cancer|Familial_cancer_of_breast|Ovarian_neoplasm|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Orofacial_cleft": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 6,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 13,
    "not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Familial_cancer_of_breast|not_provided|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 10,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 6,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer": 4,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Prostate_cancer|not_specified|CDH1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1": 1,
    "not_specified|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 8,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|Malignant_tumor_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 18,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|not_provided|Ovarian_cancer": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Familial_cancer_of_breast|Prostate_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 6,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 5,
    "not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 12,
    "Blepharocheilodontic_syndrome_1": 7,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided|Blepharocheilodontic_syndrome_1|Ovarian_cancer|Endometrial_carcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Malignant_tumor_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Diffuse_gastric_and_lobular_breast_cancer_syndrome_with_cleft_lip_and_with_or_without_cleft_palate": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 18,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Malignant_tumor_of_breast|Prostate_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 2,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "not_provided|Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_disorder": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Ovarian_neoplasm|Prostate_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Prostate_cancer|Familial_cancer_of_breast|Ovarian_neoplasm|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|CDH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Anophthalmia-microphthalmia_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Ovarian_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_cancer|_susceptibility_to|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Ovarian_neoplasm|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Breast_and/or_ovarian_cancer|Ovarian_cancer|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Cleft_lip_with_or_without_cleft_palate": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Cleft_lip_with_or_without_cleft_palate|not_provided|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Malignant_tumor_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast_lobular_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder": 4,
    "not_specified|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 14,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Ovarian_cancer|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Familial_cancer_of_breast|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 12,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer|Neoplasm_of_stomach|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|Colon_cancer|not_provided|not_specified": 1,
    "CDH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 1,
    "Cleft_lip/palate|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 2,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_cancer|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|Prostate_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Familial_cancer_of_breast|Familial_prostate_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Gastric_cancer|Ovarian_neoplasm|Prostate_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_disorder|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 3,
    "Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Prostate_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Spinocerebellar_ataxia_45|Familial_cancer_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Prostate_cancer|Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "not_provided|Ovarian_cancer|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Diffuse_gastric_and_lobular_breast_cancer_syndrome_with_cleft_lip_and_with_or_without_cleft_palate|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Prostate_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "not_provided|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Prostate_cancer|not_provided": 1,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Blepharocheilodontic_syndrome_1|Familial_cancer_of_breast|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Familial_cancer_of_breast|Prostate_cancer|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|CDH1-related_disorder|Malignant_tumor_of_breast": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Prostate_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Neoplasm_of_stomach|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 1,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 2,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder": 1,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma|Endometrial_carcinoma|Ovarian_cancer": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Blepharocheilodontic_syndrome_1|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 6,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Prostate_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Prostate_cancer|Familial_cancer_of_breast|Ovarian_neoplasm|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|not_specified|CDH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_provided": 2,
    "not_provided|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 1,
    "Breast_carcinoma|Cleft_lip_with_or_without_cleft_palate|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer|Familial_cancer_of_breast|Ovarian_neoplasm": 1,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 2,
    "Familial_cancer_of_breast|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder": 1,
    "Familial_cancer_of_breast|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "CDH1-related_disorder|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Blepharocheilodontic_syndrome_1|Familial_cancer_of_breast|Ovarian_cancer|Endometrial_carcinoma": 1,
    "Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 3,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Malignant_tumor_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Carcinoma_of_colon|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Blepharocheilodontic_syndrome_1": 1,
    "Carcinoma_of_colon|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 2,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Ovarian_cancer|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Prostate_cancer|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 3,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided": 2,
    "Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_neoplasm|Prostate_cancer|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Prostate_cancer|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Endometrial_carcinoma|Prostate_cancer|Blepharocheilodontic_syndrome_1|Ovarian_neoplasm|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Prostate_cancer|Malignant_tumor_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|not_provided": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Prostate_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|CDH1-related_disorder|Breast_and/or_ovarian_cancer|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Endometrial_carcinoma|Ovarian_cancer|Blepharocheilodontic_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 1,
    "Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Blepharocheilodontic_syndrome_1|Ovarian_neoplasm|Endometrial_carcinoma|Prostate_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Endometrial_carcinoma": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Familial_cancer_of_breast|Ovarian_cancer|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 2,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_disorder|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Prostate_cancer|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|not_specified": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_specified|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_disorder|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 2,
    "CDH1-related_disorder|not_specified|Familial_cancer_of_breast|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|not_provided": 1,
    "Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|not_specified": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Blepharocheilodontic_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_neoplasm|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Ovarian_cancer|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|Familial_cancer_of_breast|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_neoplasm|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Prostate_cancer": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|CDH1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast": 1,
    "Ovarian_neoplasm|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 1,
    "CDH1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 1,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_provided|CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Familial_cancer_of_breast|Endometrial_carcinoma|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|not_provided|Prostate_cancer": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Neoplasm_of_stomach|not_provided": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Prostate_cancer|Ovarian_neoplasm|Hereditary_diffuse_gastric_adenocarcinoma|Endometrial_carcinoma|Blepharocheilodontic_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "Breast_and/or_ovarian_cancer|CDH1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "not_provided|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Ovarian_neoplasm|Endometrial_carcinoma|Prostate_cancer|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Blepharocheilodontic_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_specified|not_provided|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma": 1,
    "Ovarian_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Endometrial_carcinoma|Ovarian_cancer|Familial_cancer_of_breast|Blepharocheilodontic_syndrome_1": 1,
    "Malignant_tumor_of_breast|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|CDH1-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_diffuse_gastric_adenocarcinoma|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "CDH1-related_disorder|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_specified|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Malignant_tumor_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|CDH1-related_disorder|not_specified|Familial_cancer_of_breast|Hereditary_diffuse_gastric_adenocarcinoma|Ovarian_cancer|Blepharocheilodontic_syndrome_1|Endometrial_carcinoma|not_provided": 1,
    "CDH1-related_disorder|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|not_provided": 1,
    "not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|Hereditary_diffuse_gastric_adenocarcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome|not_provided|Hereditary_diffuse_gastric_adenocarcinoma": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|Familial_cancer_of_breast|Ovarian_cancer|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_diffuse_gastric_adenocarcinoma|not_provided|CDH1-related_diffuse_gastric_and_lobular_breast_cancer_syndrome": 1,
    "Hereditary_North_American_Indian_childhood_cirrhosis": 15,
    "UTP4-related_disorder": 31,
    "not_specified|UTP4-related_disorder|not_provided": 1,
    "Hereditary_North_American_Indian_childhood_cirrhosis|not_provided": 3,
    "Hereditary_North_American_Indian_childhood_cirrhosis|not_provided|UTP4-related_disorder": 2,
    "not_specified|UTP4-related_disorder": 1,
    "not_provided|UTP4-related_disorder": 5,
    "UTP4-related_disorder|not_provided": 4,
    "not_provided|Hereditary_North_American_Indian_childhood_cirrhosis": 8,
    "UTP4-related_disorder|not_provided|Hereditary_North_American_Indian_childhood_cirrhosis": 2,
    "Hereditary_North_American_Indian_childhood_cirrhosis|UTP4-related_disorder": 2,
    "Hereditary_North_American_Indian_childhood_cirrhosis|UTP4-related_disorder|not_provided": 2,
    "UTP4-related_disorder|Hereditary_North_American_Indian_childhood_cirrhosis": 1,
    "not_specified|not_provided|Hereditary_North_American_Indian_childhood_cirrhosis": 1,
    "not_provided|Hereditary_North_American_Indian_childhood_cirrhosis|UTP4-related_disorder": 1,
    "Hereditary_North_American_Indian_childhood_cirrhosis|not_specified|UTP4-related_disorder": 1,
    "not_provided|UTP4-related_disorder|Hereditary_North_American_Indian_childhood_cirrhosis": 1,
    "not_provided|not_specified|UTP4-related_disorder": 1,
    "Cerebellar_hypoplasia-intellectual_disability-congenital_microcephaly-dystonia-anemia-growth_retardation_syndrome": 8,
    "Cerebellar_hypoplasia-intellectual_disability-congenital_microcephaly-dystonia-anemia-growth_retardation_syndrome|Syndromic_congenital_hemolytic_and_dyserythropoietic_anemia": 2,
    "VPS4A-related_disorder": 4,
    "Cerebellar_hypoplasia-intellectual_disability-congenital_microcephaly-dystonia-anemia-growth_retardation_syndrome|not_provided": 2,
    "Cerebellar_hypoplasia-intellectual_disability-congenital_microcephaly-dystonia-anemia-growth_retardation_syndrome|Syndromic_congenital_hemolytic_and_dyserythropoietic_anemia|not_provided": 1,
    "Inborn_genetic_diseases|VPS4A-related_disorder": 1,
    "COG8-congenital_disorder_of_glycosylation": 95,
    "not_provided|COG8-congenital_disorder_of_glycosylation": 7,
    "not_specified|COG8-congenital_disorder_of_glycosylation": 4,
    "COG8-congenital_disorder_of_glycosylation|not_specified": 3,
    "COG8-related_disorder": 2,
    "COG8-related_disorder|COG8-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "COG8-congenital_disorder_of_glycosylation|not_provided": 7,
    "COG8-related_disorder|COG8-congenital_disorder_of_glycosylation": 1,
    "COG8-related_disorder|not_specified|not_provided|COG8-congenital_disorder_of_glycosylation": 1,
    "COG8-congenital_disorder_of_glycosylation|COG8-related_disorder|not_provided": 1,
    "COG8-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 6,
    "not_provided|Congenital_disorder_of_glycosylation|COG8-congenital_disorder_of_glycosylation": 1,
    "COG8-congenital_disorder_of_glycosylation|not_provided|not_specified": 2,
    "not_specified|not_provided|COG8-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|COG8-congenital_disorder_of_glycosylation": 10,
    "COG8-congenital_disorder_of_glycosylation|COG8-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|COG8-congenital_disorder_of_glycosylation": 1,
    "not_provided|COG8-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 2,
    "COG8-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|COG8-congenital_disorder_of_glycosylation": 2,
    "COG8-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "COG8-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases|COG8-related_disorder": 1,
    "not_provided|COG8-related_disorder": 1,
    "TERF2-related_disorder": 5,
    "TERF2-related_disorder|not_provided": 1,
    "NFAT5-related_disorder": 5,
    "Immunodeficiency|not_specified": 27,
    "not_provided|Immunodeficiency|not_specified": 1,
    "NFAT5-related_disorder|Immunodeficiency": 4,
    "Immunodeficiency|NFAT5-related_disorder": 8,
    "NFAT5-related_disorder|not_provided|Immunodeficiency": 4,
    "Immunodeficiency|not_provided": 5,
    "Immunodeficiency_and_Autoimmune_Enterocolopathy|not_specified|Immunodeficiency": 1,
    "not_specified|NFAT5-related_disorder": 1,
    "not_specified|not_provided|NFAT5-related_disorder|Immunodeficiency": 1,
    "not_provided|Immunodeficiency|NFAT5-related_disorder": 1,
    "NFAT5-related_disorder|not_specified|Immunodeficiency": 2,
    "not_specified|NFAT5-related_disorder|Immunodeficiency": 1,
    "Immunodeficiency|not_specified|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency": 1,
    "NFAT5-related_disorder|not_provided|Immunodeficiency|not_specified": 1,
    "NFAT5-related_disorder|Immunodeficiency|not_provided": 1,
    "NQO1-related_disorder|not_specified": 1,
    "NQO1-related_disorder|Benzene_toxicity|_susceptibility_to": 1,
    "NQO1-related_disorder": 2,
    "Spondyloepiphyseal_dysplasia_MIR140_type_Nishimura|Spondyloepiphyseal_dysplasia|_nishimura_type": 1,
    "not_provided|PDPR-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N": 23,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|not_provided": 4,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_29": 16,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_29|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "AARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2N|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N": 9,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_axonal_type_2N|not_provided": 1,
    "Trichothiodystrophy_8|_nonphotosensitive": 4,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "AARS1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases": 2,
    "AARS1-related_disorder|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "AARS1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases": 5,
    "Charcot-Marie-Tooth_disease_type_2|AARS1-related_disorder": 3,
    "AARS1-related_disorder": 3,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_type_2|Trichothiodystrophy_8|_nonphotosensitive": 2,
    "Inborn_genetic_diseases|AARS-related_disorder|AARS1-related_disorder|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_type_2|not_provided": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|not_provided": 3,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|not_provided|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "AARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|not_specified": 1,
    "not_provided|AARS1-related_disorder|Charcot-Marie-Tooth_disease_type_2": 1,
    "Trichothiodystrophy_8|_nonphotosensitive|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Impaired_vibration_sensation_in_the_lower_limbs|Shuffling_gait|Distal_muscle_weakness|EMG:_neuropathic_changes|Gait_disturbance|Progressive_distal_muscular_atrophy|Foot_dorsiflexor_weakness|Clubfoot": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2": 9,
    "Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|AARS1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2|AARS1-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_29|Trichothiodystrophy_8|_nonphotosensitive": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|AARS1-related_disorder|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|not_specified|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 3,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_2|Developmental_and_epileptic_encephalopathy|_29|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "AARS1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2N|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|AARS1-related_disorder|Trichothiodystrophy_8|_nonphotosensitive|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Developmental_and_epileptic_encephalopathy|_29": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Trichothiodystrophy_8|_nonphotosensitive|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Developmental_and_epileptic_encephalopathy|_29": 2,
    "AARS1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Peripheral_neuropathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2": 1,
    "Inborn_genetic_diseases|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|not_specified|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Developmental_and_epileptic_encephalopathy|_29": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|not_provided": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|AARS1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2|AARS1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Trichothiodystrophy_8|_nonphotosensitive|Charcot-Marie-Tooth_disease_type_2|AARS1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2|AARS1-related_disorder": 1,
    "Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Hereditary_diffuse_leukoencephalopathy_with_spheroids": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_29|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_29": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N": 1,
    "See_cases|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Developmental_and_epileptic_encephalopathy|_29": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_axonal_type_2N|AARS1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2N|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2N|Developmental_and_epileptic_encephalopathy|_29|Leukoencephalopathy|_hereditary_diffuse|_with_spheroids_2|Trichothiodystrophy_8|_nonphotosensitive|not_specified": 1,
    "FCSK-related_disorder": 8,
    "FCSK-related_disorder|not_provided": 23,
    "not_provided|Congenital_disorder_of_glycosylation_with_defective_fucosylation_2": 3,
    "not_specified|FCSK-related_disorder": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_2|not_specified|not_provided": 1,
    "not_provided|FCSK-related_disorder": 15,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_2": 10,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_2|not_provided": 5,
    "not_specified|FCSK-related_disorder|not_provided": 1,
    "not_specified|not_provided|FCSK-related_disorder": 3,
    "not_provided|Congenital_disorder_of_glycosylation_with_defective_fucosylation_2|not_specified": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_2|not_provided|FCSK-related_disorder": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation_2|not_specified": 2,
    "not_provided|not_specified|Congenital_disorder_of_glycosylation_with_defective_fucosylation_2": 2,
    "not_specified|Congenital_disorder_of_glycosylation_with_defective_fucosylation_2": 1,
    "Congenital_disorder_of_glycosylation_with_defective_fucosylation|not_provided|Congenital_disorder_of_glycosylation_with_defective_fucosylation_2": 1,
    "FCSK-related_disorder|not_specified|not_provided": 1,
    "COG4-related_disorder|not_specified": 1,
    "not_provided|COG4-congenital_disorder_of_glycosylation": 11,
    "COG4-congenital_disorder_of_glycosylation": 108,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type": 7,
    "COG4-related_disorder": 13,
    "Inborn_genetic_diseases|COG4-congenital_disorder_of_glycosylation": 10,
    "not_specified|COG4-congenital_disorder_of_glycosylation": 3,
    "COG4-related_disorder|not_provided|COG4-congenital_disorder_of_glycosylation": 1,
    "not_provided|not_specified|COG4-congenital_disorder_of_glycosylation": 2,
    "not_provided|COG4-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "COG4-congenital_disorder_of_glycosylation|not_provided|See_cases": 1,
    "not_specified|not_provided|COG4-congenital_disorder_of_glycosylation": 3,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|COG4-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|COG4-congenital_disorder_of_glycosylation": 1,
    "COG4-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|COG4-congenital_disorder_of_glycosylation|COG4-related_disorder": 2,
    "COG4-congenital_disorder_of_glycosylation|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type": 4,
    "not_provided|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|COG4-congenital_disorder_of_glycosylation": 1,
    "COG4-congenital_disorder_of_glycosylation|not_provided": 3,
    "Inborn_genetic_diseases|COG4-congenital_disorder_of_glycosylation|not_provided": 1,
    "Delayed_gross_motor_development|COG4-congenital_disorder_of_glycosylation|not_provided|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type": 1,
    "COG4-related_disorder|not_specified|not_provided|COG4-congenital_disorder_of_glycosylation": 1,
    "COG4-related_disorder|not_provided": 1,
    "COG4-congenital_disorder_of_glycosylation|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|not_provided|Inborn_genetic_diseases": 1,
    "COG4-congenital_disorder_of_glycosylation|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|COG4-congenital_disorder_of_glycosylation|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type": 1,
    "COG4-congenital_disorder_of_glycosylation|not_provided|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type": 1,
    "COG4-related_disorder|COG4-congenital_disorder_of_glycosylation|not_provided": 1,
    "COG4-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 4,
    "not_specified|not_provided|COG4-congenital_disorder_of_glycosylation|COG4-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|COG4-congenital_disorder_of_glycosylation": 1,
    "COG4-related_disorder|not_provided|COG4-congenital_disorder_of_glycosylation|not_specified": 1,
    "not_specified|COG4-congenital_disorder_of_glycosylation|not_provided|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type": 1,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|COG4-congenital_disorder_of_glycosylation": 1,
    "COG4-congenital_disorder_of_glycosylation|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|not_provided|not_specified": 1,
    "not_provided|not_specified|COG4-related_disorder|COG4-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|COG4-congenital_disorder_of_glycosylation|Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|not_provided": 1,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|not_provided": 1,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|not_specified|not_provided|COG4-congenital_disorder_of_glycosylation": 1,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|Inborn_genetic_diseases": 1,
    "COG4-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "COG4-congenital_disorder_of_glycosylation|COG4-related_disorder": 1,
    "Microcephalic_osteodysplastic_dysplasia|_Saul-Wilson_type|COG4-congenital_disorder_of_glycosylation|not_provided": 1,
    "Inborn_genetic_diseases|COG4-related_disorder": 1,
    "IL34-related_disorder": 3,
    "Intellectual_developmental_disorder_with_ocular_anomalies_and_distinctive_facial_features": 6,
    "Intellectual_developmental_disorder_with_ocular_anomalies_and_distinctive_facial_features|not_specified|Syndromic_intellectual_disability|not_provided|MTSS2-related_neurodevelopmental_disorder": 1,
    "Intellectual_developmental_disorder_with_ocular_anomalies_and_distinctive_facial_features|not_specified": 1,
    "Hypotonia|Iron_deposition_in_globus_pallidus|Microcephaly|Intellectual_disability|Global_developmental_delay": 1,
    "not_provided|VAC14-related_disorder": 6,
    "not_provided|Striatonigral_degeneration|_childhood-onset": 3,
    "Striatonigral_degeneration|_childhood-onset": 14,
    "Striatonigral_degeneration|_childhood-onset|Inborn_genetic_diseases|not_provided": 2,
    "Yunis-Varon_syndrome|not_provided": 1,
    "Striatonigral_degeneration|_childhood-onset|not_provided": 4,
    "Striatonigral_degeneration|_childhood-onset|Inborn_genetic_diseases": 1,
    "VAC14-related_disorder|not_provided": 5,
    "Striatonigral_degeneration|_childhood-onset|not_provided|Yunis-Varon_syndrome": 1,
    "VAC14-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "HYDIN-related_disorder": 4,
    "Primary_ciliary_dyskinesia_5": 100,
    "Primary_ciliary_dyskinesia_5|not_provided": 7,
    "not_specified|Primary_ciliary_dyskinesia_5": 1,
    "Primary_ciliary_dyskinesia_5|Inborn_genetic_diseases": 2,
    "not_provided|Primary_ciliary_dyskinesia_5": 3,
    "not_specified|Primary_ciliary_dyskinesia_5|not_provided": 2,
    "not_provided|not_specified|Primary_ciliary_dyskinesia_5": 1,
    "HYDIN-related_disorder|not_provided": 1,
    "not_provided|HYDIN-related_disorder|Primary_ciliary_dyskinesia_5": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_5": 1,
    "Hypertyrosinemia": 6,
    "Tyrosinemia_type_II": 411,
    "not_provided|Tyrosinemia_type_II": 6,
    "Tyrosinemia_type_II|not_specified": 2,
    "not_specified|not_provided|Tyrosinemia_type_II": 1,
    "Inborn_genetic_diseases|Tyrosinemia_type_II": 2,
    "Tyrosinemia_type_II|Inborn_genetic_diseases": 5,
    "not_provided|TAT-related_disorder|Tyrosinemia_type_II": 1,
    "Inborn_genetic_diseases|TAT-related_disorder|Tyrosinemia_type_II": 1,
    "Microcephaly|Tyrosinemia_type_II": 1,
    "Tyrosinemia_type_II|TAT-related_disorder": 1,
    "not_provided|Tyrosinemia_type_II|not_specified": 2,
    "Tyrosinemia_type_II|not_provided": 4,
    "TAT-related_disorder": 1,
    "AP1G1-related_disorder": 12,
    "Usmani-Riazuddin_syndrome|_autosomal_dominant": 20,
    "Usmani-Riazuddin_syndrome|_autosomal_dominant|Usmani-Riazuddin_syndrome|_autosomal_recessive": 3,
    "not_provided|Usmani-Riazuddin_syndrome|_autosomal_recessive": 1,
    "Usmani-Riazuddin_syndrome|_autosomal_recessive": 2,
    "not_provided|Usmani-Riazuddin_syndrome|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "not_provided|Essential_tremor": 1,
    "Miller_syndrome|not_provided": 3,
    "not_provided|DHODH-related_disorder": 1,
    "Miller_syndrome": 53,
    "DHODH-related_disorder": 6,
    "not_specified|not_provided|Miller_syndrome": 3,
    "not_provided|Miller_syndrome": 23,
    "Inborn_genetic_diseases|not_provided|Miller_syndrome": 1,
    "not_provided|DHODH-related_disorder|Miller_syndrome": 3,
    "Miller_syndrome|not_specified|not_provided": 1,
    "not_provided|Miller_syndrome|DHODH-related_disorder": 1,
    "DHODH-related_disorder|Miller_syndrome": 1,
    "Miller_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Miller_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Miller_syndrome": 2,
    "DHODH-related_disorder|not_provided": 2,
    "Miller_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "HAPTOGLOBIN|_ALPHA-1|_FAST-SLOW_POLYMORPHISM": 1,
    "HP-related_disorder": 3,
    "not_provided|HP-related_disorder": 2,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_84": 3,
    "not_specified|DHX38-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_84|Retinal_dystrophy": 3,
    "Retinitis_pigmentosa_84|not_provided": 4,
    "DHX38-related_disorder|not_provided": 4,
    "not_specified|not_provided|Retinitis_pigmentosa_84": 2,
    "Retinitis_pigmentosa_84|Autosomal_recessive_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_84": 2,
    "not_provided|Retinitis_pigmentosa_84": 5,
    "not_provided|DHX38-related_disorder": 5,
    "not_provided|DHX38-related_disorder|not_specified": 1,
    "Retinal_dystrophy|not_provided|DHX38-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_84|DHX38-related_disorder": 1,
    "DHX38-related_disorder|not_provided|Retinal_dystrophy": 1,
    "PMFBP1-related_disorder": 14,
    "Spermatogenic_failure_31": 11,
    "PMFBP1-related_disorder|not_provided|Spermatogenic_failure_31": 1,
    "not_provided|PMFBP1-related_disorder": 1,
    "PMFBP1-related_disorder|not_provided": 2,
    "Oligospermia|Abnormal_sperm_morphology": 1,
    "not_provided|ZFHX3-related_disorder": 27,
    "ZFHX3-related_disorder": 91,
    "ZFHX3-related_disorder|not_provided": 18,
    "not_provided|not_specified|Prostate_cancer|_somatic": 1,
    "not_provided|ZFHX3-related_disorder|not_specified": 1,
    "ZFHX3-related_disorder|not_specified|not_provided": 1,
    "ZFHX3-related_disorder|not_specified": 1,
    "ZFHX3-associated_disorder": 1,
    "ZFHX3-associated_neurodevelopmental_disorder": 1,
    "not_specified|ZFHX3-related_disorder": 1,
    "Atrial_fibrillation|_familial|_8": 1,
    "Fanconi_anemia|_complementation_group_W|RFWD3-related_disorder|not_provided": 1,
    "not_provided|RFWD3-related_disorder|not_specified": 2,
    "RFWD3-related_disorder|not_provided": 6,
    "not_provided|Fanconi_anemia|_complementation_group_W": 6,
    "Fanconi_anemia|_complementation_group_W|not_provided": 4,
    "not_provided|not_specified|RFWD3-related_disorder": 1,
    "RFWD3-related_disorder": 3,
    "Fanconi_anemia|_complementation_group_W|not_specified|not_provided": 2,
    "not_provided|RFWD3-related_disorder": 4,
    "Fanconi_anemia|_complementation_group_W": 2,
    "not_specified|not_provided|RFWD3-related_disorder": 1,
    "Chronic_multifocal_osteomyelitis": 2,
    "Hereditary_spastic_paraplegia_35": 67,
    "Hereditary_spastic_paraplegia_35|not_provided": 4,
    "not_provided|Hereditary_spastic_paraplegia_35": 9,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_35|not_provided": 3,
    "not_specified|Hereditary_spastic_paraplegia_35|not_provided|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_35|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_provided": 1,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_35|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_35": 1,
    "Hereditary_spastic_paraplegia_35|Inborn_genetic_diseases|Spastic_paraplegia|not_provided": 2,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_35": 1,
    "FA2H-related_disorder": 2,
    "not_provided|Hereditary_spastic_paraplegia_35|Spastic_paraplegia|not_specified|Spastic_ataxia": 1,
    "Tip-toe_gait|Cerebellar_atrophy": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_35": 4,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_35|not_provided": 1,
    "FA2H-related_disorder|Spastic_paraplegia": 2,
    "not_provided|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35": 1,
    "not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35": 1,
    "not_specified|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_35": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35|Spastic_paraplegia|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_35|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_35|FA2H-related_disorder": 1,
    "Hereditary_spastic_paraplegia_35|Spastic_paraplegia": 4,
    "Hereditary_spastic_paraplegia_35|Spastic_paraplegia|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_35|Intellectual_disability": 1,
    "Hereditary_spastic_paraplegia_35|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|not_provided": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35": 1,
    "Hereditary_spastic_paraplegia_35|not_provided|Spastic_paraplegia": 4,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_35|not_provided|not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia_35": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation|Hereditary_spastic_paraplegia_35|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_35|Neurodegeneration_with_brain_iron_accumulation|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35": 1,
    "Hereditary_spastic_paraplegia_35|Hereditary_spastic_paraplegia|Spastic_paraplegia|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35|not_specified": 1,
    "not_specified|Hereditary_spastic_paraplegia_35|Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Spastic_paraplegia|not_provided": 1,
    "not_specified|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35": 1,
    "not_provided|Hereditary_spastic_paraplegia_35|Spastic_paraplegia": 2,
    "Neurodegeneration_with_brain_iron_accumulation|Spastic_paraplegia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_35|Spastic_paraplegia": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_35": 1,
    "Lactic_aciduria_due_to_D-lactic_acid": 10,
    "Lactic_aciduria_due_to_D-lactic_acid|Abnormal_circulating_lactate_dehydrogenase_concentration": 1,
    "not_provided|LDHD-related_disorder": 4,
    "Abnormal_circulating_lactate_dehydrogenase_concentration|Lactic_aciduria_due_to_D-lactic_acid": 1,
    "LDHD-related_disorder": 6,
    "LDHD-related_disorder|not_provided": 2,
    "CFDP1-related_disorder": 7,
    "Macular_corneal_dystrophy": 239,
    "not_provided|Macular_corneal_dystrophy": 16,
    "Macular_corneal_dystrophy|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|Macular_corneal_dystrophy": 2,
    "Macular_corneal_dystrophy|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Macular_corneal_dystrophy": 7,
    "Macular_corneal_dystrophy|not_provided|Inborn_genetic_diseases": 1,
    "CHST6-related_disorder": 3,
    "CHST6-related_disorder|Macular_corneal_dystrophy": 1,
    "CHST6-related_disorder|not_provided|Macular_corneal_dystrophy|Macular_corneal_dystrophy|_type_II": 1,
    "Macular_corneal_dystrophy|not_provided": 1,
    "not_provided|CHST6-related_disorder|Macular_corneal_dystrophy": 1,
    "Macular_corneal_dystrophy|CHST6-related_disorder": 1,
    "CHST6-related_disorder|Macular_corneal_dystrophy|not_provided": 1,
    "Macular_corneal_dystrophy|_type_II": 1,
    "CHST6-related_disorder|not_provided|Macular_corneal_dystrophy": 1,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20": 146,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11": 141,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided|TMEM231-related_disorder": 1,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided|not_specified": 4,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided": 7,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|not_provided": 3,
    "Inborn_genetic_diseases|Joubert_syndrome_20|Meckel_syndrome|_type_11|not_provided": 4,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|not_specified": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_20|Meckel_syndrome|_type_11": 10,
    "not_provided|Joubert_syndrome_20|Meckel_syndrome|_type_11": 10,
    "not_provided|TMEM231-related_disorder|Joubert_syndrome_20|Meckel_syndrome|_type_11|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_11|Joubert_syndrome_20": 6,
    "Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_11": 1,
    "not_provided|Joubert_syndrome_20|Meckel_syndrome|_type_11|Inborn_genetic_diseases": 2,
    "TMEM231-related_disorder|not_provided|Joubert_syndrome_20|Meckel_syndrome|_type_11|not_specified": 1,
    "TMEM231-related_disorder|Joubert_syndrome_20|Meckel_syndrome|_type_11": 3,
    "not_provided|Meckel_syndrome|_type_11|Joubert_syndrome_20|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_11": 4,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|TMEM231-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Joubert_syndrome_20|Meckel_syndrome|_type_11": 3,
    "not_provided|Meckel_syndrome|_type_11|Joubert_syndrome_20": 4,
    "Inborn_genetic_diseases|not_specified|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided|TMEM231-related_disorder": 1,
    "TMEM231-related_disorder|not_provided|Joubert_syndrome_20|Meckel_syndrome|_type_11": 1,
    "Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_11|Joubert_syndrome_20": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_20|Meckel_syndrome|_type_11|not_provided|TMEM231-related_disorder": 1,
    "Joubert_syndrome_20|TMEM231-related_disorder": 1,
    "TMEM231-related_disorder|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_20|Meckel_syndrome|_type_11|not_provided|Joubert_syndrome_and_related_disorders|TMEM231-related_disorder": 1,
    "not_provided|TMEM231-related_disorder|Joubert_syndrome_20|Meckel_syndrome|_type_11": 2,
    "not_provided|Inborn_genetic_diseases|Meckel_syndrome|_type_11|Joubert_syndrome_20": 1,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|Inborn_genetic_diseases": 2,
    "not_specified|Joubert_syndrome_20|Meckel_syndrome|_type_11": 1,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|not_specified|not_provided": 2,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|not_provided|not_specified": 1,
    "not_specified|Joubert_syndrome_20|Meckel_syndrome|_type_11|TMEM231-related_disorder|not_provided": 1,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|not_specified": 5,
    "Ciliopathy|Meckel_syndrome|_type_11|Joubert_syndrome_20|TMEM231-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Joubert_syndrome_20|Meckel_syndrome|_type_11": 1,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|not_specified|not_provided": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome_20|Meckel_syndrome|_type_11": 1,
    "not_provided|not_specified|Joubert_syndrome_20|Meckel_syndrome|_type_11": 1,
    "not_provided|Joubert_syndrome_20|Orofacial-digital_syndrome_III|Inborn_genetic_diseases|Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_11": 1,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|Inborn_genetic_diseases": 3,
    "Joubert_syndrome_20|Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_11": 1,
    "Joubert_syndrome_20|Inborn_genetic_diseases": 1,
    "TMEM231-related_disorder|Joubert_syndrome_20|Meckel_syndrome|_type_11|Ciliopathy|not_provided": 1,
    "not_provided|Joubert_syndrome|Joubert_syndrome_20|Meckel_syndrome|_type_11|Inborn_genetic_diseases": 1,
    "not_provided|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_specified": 2,
    "not_specified|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided": 1,
    "Meckel_syndrome|_type_11|Joubert_syndrome_20|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided": 1,
    "TMEM231-related_disorder": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Meckel_syndrome|_type_11": 1,
    "Inborn_genetic_diseases|not_provided|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_specified": 1,
    "Joubert_syndrome_20|Meckel_syndrome|_type_11|not_provided|TMEM231-related_disorder": 1,
    "TMEM231-related_disorder|Joubert_syndrome_20|Meckel_syndrome|_type_11|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TMEM231-related_disorder|Meckel_syndrome|_type_11|Joubert_syndrome_20": 1,
    "TMEM231-related_disorder|Meckel_syndrome|_type_11|Joubert_syndrome_20|not_provided|not_specified": 1,
    "not_specified|not_provided|Joubert_syndrome_20|Meckel_syndrome|_type_11": 1,
    "not_provided|TMEM231-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89|not_provided|not_specified": 1,
    "KARS1-related_disorder|not_provided": 7,
    "LEUKOENCEPHALOPATHY|_PROGRESSIVE|_INFANTILE-ONSET|_WITH_DEAFNESS": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89": 6,
    "not_provided|Inborn_genetic_diseases|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 1,
    "KARS1-related_disorder": 9,
    "not_provided|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 1,
    "Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 7,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_B|not_provided|not_specified": 2,
    "Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|not_provided": 1,
    "Deafness|_congenital|_and_adult-onset_progressive_leukoencephalopathy": 1,
    "KARS1-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89|Leukodystrophy|Global_developmental_delay|not_provided|Sensorineural_hearing_loss_disorder": 1,
    "LEUKOENCEPHALOPATHY|_PROGRESSIVE|_INFANTILE-ONSET|_WITH_DEAFNESS|Deafness|_congenital|_and_adult-onset_progressive_leukoencephalopathy|Autosomal_recessive_nonsyndromic_hearing_loss_89": 1,
    "LEUKOENCEPHALOPATHY|_PROGRESSIVE|_INFANTILE-ONSET|_WITH_DEAFNESS|Lactic_acidosis|Sensorineural_hearing_loss_disorder|Global_developmental_delay|Hypotonia|not_provided": 1,
    "Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|KARS1-related_disorder": 1,
    "not_specified|not_provided|KARS1-related_disorder": 1,
    "KARS1-related_disorder|not_provided|Hearing_impairment|Charcot-Marie-Tooth_disease_recessive_intermediate_B|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89|not_provided": 1,
    "not_specified|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89|not_specified|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_89": 1,
    "not_provided|Abnormal_cerebral_white_matter_morphology|Abnormal_pyramidal_sign|Congenital_sensorineural_hearing_impairment|Progressive_cerebellar_ataxia|Optic_neuropathy|Deafness|_congenital|_and_adult-onset_progressive_leukoencephalopathy|Autosomal_recessive_nonsyndromic_hearing_loss_89": 1,
    "Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|not_specified|not_provided": 1,
    "not_provided|not_specified|KARS1-related_disorder": 1,
    "Abnormal_pyramidal_sign|Congenital_sensorineural_hearing_impairment|Progressive_cerebellar_ataxia|Abnormal_cerebral_white_matter_morphology|Optic_neuropathy|KARS-related_disorder|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|Deafness|_congenital|_and_adult-onset_progressive_leukoencephalopathy|LEUKOENCEPHALOPATHY|_PROGRESSIVE|_INFANTILE-ONSET|_WITH_DEAFNESS|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_89|Hearing_loss|_autosomal_recessive|Charcot-Marie-Tooth_disease_recessive_intermediate_B|KARS1-related_disorder": 1,
    "not_provided|KARS1-related_disorder": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|Nonsyndromic_genetic_hearing_loss": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_B": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_89|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_B|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_89|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|Deafness|_congenital|_and_adult-onset_progressive_leukoencephalopathy|Charcot-Marie-Tooth_disease_recessive_intermediate_B": 1,
    "Global_developmental_delay|Seizure|Nystagmus|Microcephaly": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_recessive_intermediate_B|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_recessive_intermediate_B|Autosomal_recessive_nonsyndromic_hearing_loss_89|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|Deafness|_congenital|_and_adult-onset_progressive_leukoencephalopathy": 1,
    "KARS1-related_disorder|not_provided|Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness": 1,
    "Leukoencephalopathy|_progressive|_infantile-onset|_with_or_without_deafness|KARS1-related_disorder|not_provided": 1,
    "CNTNAP4-related_disorder": 8,
    "not_provided|Inborn_genetic_diseases|ADAMTS18-related_disorder": 1,
    "Microcornea-myopic_chorioretinal_atrophy|not_provided": 3,
    "ADAMTS18-related_disorder|not_provided": 21,
    "Inborn_genetic_diseases|not_provided|ADAMTS18-related_disorder": 1,
    "not_provided|Microcornea-myopic_chorioretinal_atrophy|Retinitis_pigmentosa|ADAMTS18-related_disorder": 1,
    "not_provided|Microcornea-myopic_chorioretinal_atrophy": 1,
    "not_provided|ADAMTS18-related_disorder": 8,
    "Inborn_genetic_diseases|Retinal_dystrophy|Microcornea-myopic_chorioretinal_atrophy|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|ADAMTS18-related_disorder|not_provided": 1,
    "not_provided|Microcornea-myopic_chorioretinal_atrophy|Inborn_genetic_diseases": 1,
    "ADAMTS18-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Microcornea-myopic_chorioretinal_atrophy": 6,
    "ADAMTS18-related_disorder": 2,
    "Microcornea-myopic_chorioretinal_atrophy|not_specified|not_provided": 1,
    "not_provided|Knobloch_syndrome": 38,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|not_provided|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 282,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 244,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 22,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 8,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 8,
    "Developmental_and_epileptic_encephalopathy|_28": 27,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 7,
    "WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 2,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28": 4,
    "Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 3,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided": 13,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 11,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_28|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases": 11,
    "See_cases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_provided|West_syndrome": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|not_specified|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_provided|Malignant_tumor_of_esophagus|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Developmental_and_epileptic_encephalopathy|_28|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided|Developmental_and_epileptic_encephalopathy|_28|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_28|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 4,
    "Autosomal_recessive_spinocerebellar_ataxia_12": 3,
    "WWOX-related_diosrder|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided": 28,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_specified": 10,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided|not_specified": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_28": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_28|Abnormality_of_the_nervous_system": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|WWOX-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_provided|Malignant_tumor_of_esophagus|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Developmental_and_epileptic_encephalopathy|_28|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_28|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Developmental_and_epileptic_encephalopathy|_28": 2,
    "WWOX-related_disorder": 3,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_28|not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_28": 3,
    "WWOX-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|not_provided|not_specified|WWOX-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 5,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_28": 2,
    "WWOX-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus": 1,
    "not_provided|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "WWOX-related_disorder|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 2,
    "Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_specified": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_28|not_provided|Developmental_and_epileptic_encephalopathy|_1|Malignant_tumor_of_esophagus|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus": 1,
    "WWOX-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_28|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided": 2,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_specified|WWOX-related_disorder|not_provided": 1,
    "Global_developmental_delay|Brain_atrophy|Abnormal_facial_shape|Developmental_and_epileptic_encephalopathy|_28|not_provided|WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Esophageal_squamous_cell_carcinoma": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_specified|not_provided": 2,
    "not_specified|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided|Inborn_genetic_diseases|See_cases": 1,
    "Malignant_tumor_of_esophagus|WWOX-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Developmental_and_epileptic_encephalopathy|_1|Abnormality_of_the_nervous_system|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_28|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases|not_provided": 5,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|WWOX-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_28|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|WWOX-related_disorder": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus|not_provided": 1,
    "See_cases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_specified|not_provided": 7,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_specified|Developmental_and_epileptic_encephalopathy|_28|not_provided": 1,
    "not_provided|Neurodevelopmental_disorders": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Esophageal_squamous_cell_carcinoma|_somatic|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|WWOX-related_disorder|not_specified|not_provided": 1,
    "not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Epileptic_encephalopathy": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28|not_provided|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28|WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_provided": 2,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided|Malignant_tumor_of_esophagus|Developmental_and_epileptic_encephalopathy|_28": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus|WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_28|Autosomal_recessive_spinocerebellar_ataxia_12|not_specified|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_28|not_provided|See_cases|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "WWOX-related_disorder|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Inborn_genetic_diseases|not_provided": 1,
    "Malignant_tumor_of_esophagus|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_28|Developmental_and_epileptic_encephalopathy|_1|not_provided|not_specified": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|not_specified|not_provided": 1,
    "WWOX-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|Intellectual_disability": 1,
    "not_specified|not_provided|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_28|Neurodevelopmental_delay": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|not_provided|not_specified": 1,
    "Global_developmental_delay|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_28|Malignant_tumor_of_esophagus|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_1|Autosomal_recessive_spinocerebellar_ataxia_12|WWOX-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_spinocerebellar_ataxia_12|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Autosomal_recessive_spinocerebellar_ataxia_12|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_28": 1,
    "not_provided|MAF-related_disorder|Cataract_21_multiple_types|Ayme-Gripp_syndrome": 1,
    "MAF-related_disorder": 11,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome": 45,
    "Ayme-Gripp_syndrome": 11,
    "Cataract_21_multiple_types": 6,
    "Inborn_genetic_diseases|Cataract_21_multiple_types|Ayme-Gripp_syndrome": 1,
    "Ayme-Gripp_syndrome|Cataract_21_multiple_types": 5,
    "not_provided|Cataract_21_multiple_types": 3,
    "Ayme-Gripp_syndrome|Cataract_21_multiple_types|not_specified": 1,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome|not_specified": 1,
    "Ayme-Gripp_syndrome|Cataract_21_multiple_types|not_provided": 3,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome|not_provided": 3,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|not_provided|Ayme-Gripp_syndrome|Cataract_21_multiple_types|Inborn_genetic_diseases": 1,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome|Inborn_genetic_diseases": 1,
    "MAF-related_disorder|not_provided|Ayme-Gripp_syndrome|Cataract_21_multiple_types": 1,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome|not_provided|not_specified": 1,
    "not_provided|Cataract_21_multiple_types|Ayme-Gripp_syndrome": 1,
    "Ayme-Gripp_syndrome|Cataract_21_multiple_types|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Cataract_21_multiple_types|Ayme-Gripp_syndrome": 1,
    "Inborn_genetic_diseases|MAF-related_disorder": 1,
    "MAF-related_disorder|not_provided": 1,
    "Cataract_21_multiple_types|Ayme-Gripp_syndrome|not_provided|Inborn_genetic_diseases|MAF-related_disorder": 1,
    "MAF-related_disorder|Cataract_21_multiple_types|Ayme-Gripp_syndrome|not_provided": 1,
    "Ayme-Gripp_syndrome|not_provided": 3,
    "MAF-related_disorder|Ayme-Gripp_syndrome|not_provided": 1,
    "not_specified|Ayme-Gripp_syndrome|not_provided|Cataract_21_multiple_types": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_7": 6,
    "not_provided|Multiple_mitochondrial_dysfunctions_syndrome_7": 1,
    "Glycine_encephalopathy|GCSH-related_disorder|not_provided": 1,
    "GCSH-related_disorder|Multiple_mitochondrial_dysfunctions_syndrome_7|not_provided|Glycine_encephalopathy": 2,
    "GCSH-related_disorder": 5,
    "Glycine_encephalopathy|GCSH-related_disorder|not_specified|not_provided": 1,
    "GCSH-related_disorder|Glycine_encephalopathy": 1,
    "Glycine_encephalopathy|not_provided|GCSH-related_disorder": 1,
    "GCSH-related_disorder|not_provided": 1,
    "Otosclerosis_4": 1,
    "BCO1-related_disorder": 6,
    "not_provided|BCO1-related_disorder": 1,
    "Hereditary_hypercarotenemia_and_vitamin_A_deficiency": 3,
    "BCO1-related_disorder|Hereditary_hypercarotenemia_and_vitamin_A_deficiency|not_specified": 1,
    "BCO1-related_disorder|not_specified": 1,
    "BCO1-related_disorder|not_provided": 1,
    "Giant_axonal_neuropathy_1": 566,
    "Giant_axonal_neuropathy_1|not_provided": 32,
    "Giant_axonal_neuropathy_1|Charcot-Marie-Tooth_disease": 2,
    "Inborn_genetic_diseases|not_provided|GAN-related_disorder|Giant_axonal_neuropathy_1": 2,
    "Inborn_genetic_diseases|Giant_axonal_neuropathy_1": 27,
    "Giant_axonal_neuropathy_1|Inborn_genetic_diseases": 31,
    "not_provided|Giant_axonal_neuropathy_1": 14,
    "Giant_axonal_neuropathy_1|not_specified": 6,
    "Inborn_genetic_diseases|not_specified|Giant_axonal_neuropathy_1": 2,
    "Giant_axonal_neuropathy": 1,
    "Inborn_genetic_diseases|not_provided|Giant_axonal_neuropathy_1": 7,
    "Charcot-Marie-Tooth_disease|Giant_axonal_neuropathy_1": 2,
    "not_specified|Giant_axonal_neuropathy_1": 6,
    "GAN-related_disorder|Inborn_genetic_diseases|Giant_axonal_neuropathy_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Giant_axonal_neuropathy_1": 4,
    "Giant_axonal_neuropathy_1|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Giant_axonal_neuropathy_1|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Giant_axonal_neuropathy_1|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|Giant_axonal_neuropathy_1": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|Giant_axonal_neuropathy_1": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Giant_axonal_neuropathy_1": 1,
    "Giant_axonal_neuropathy|Inborn_genetic_diseases|not_provided|Giant_axonal_neuropathy_1": 1,
    "GAN-related_disorder|not_specified|Giant_axonal_neuropathy_1|Inborn_genetic_diseases|not_provided": 1,
    "Giant_axonal_neuropathy_1|Peripheral_neuropathy": 1,
    "not_specified|not_provided|Giant_axonal_neuropathy_1": 1,
    "GAN-related_disorder|Inborn_genetic_diseases|not_provided|Giant_axonal_neuropathy_1": 1,
    "not_provided|not_specified|Giant_axonal_neuropathy_1": 2,
    "GAN-related_disorder": 1,
    "GAN-related_disorder|Giant_axonal_neuropathy_1": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|GAN-related_disorder|Giant_axonal_neuropathy_1": 1,
    "Giant_axonal_neuropathy_1|See_cases": 1,
    "Giant_axonal_neuropathy_1|Inborn_genetic_diseases|not_provided": 1,
    "Giant_axonal_neuropathy_1|not_specified|not_provided|GAN-related_disorder": 1,
    "GAN-related_disorder|not_provided|Giant_axonal_neuropathy_1": 1,
    "CMIP-related_disorder": 13,
    "not_provided|CMIP-related_disorder": 3,
    "CMIP-related_disorder|not_provided": 6,
    "Familial_cold_autoinflammatory_syndrome_3": 1066,
    "Familial_cold_autoinflammatory_syndrome_3|Inborn_genetic_diseases": 18,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided": 14,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_3": 22,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 4,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 15,
    "Familial_cold_autoinflammatory_syndrome_3|not_provided": 40,
    "not_specified|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided": 5,
    "not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_3": 5,
    "PLCG2-related_disorder": 8,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 82,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_provided": 9,
    "Familial_cold_autoinflammatory_syndrome_3|Inborn_genetic_diseases|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 2,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3": 34,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_specified": 2,
    "not_provided|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_specified": 1,
    "PLCG2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Familial_cold_autoinflammatory_syndrome_3": 2,
    "PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 3,
    "Inborn_genetic_diseases|not_provided|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 1,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|PLCG2-related_disorder": 3,
    "not_provided|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3": 3,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3": 40,
    "Inborn_genetic_diseases|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_provided": 1,
    "not_specified|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided|Familial_cold_autoinflammatory_syndrome_3": 1,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_provided|not_specified": 1,
    "not_provided|PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 2,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 2,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_specified|not_provided": 2,
    "PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3|not_specified": 1,
    "PLCG2-related_disorder|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_provided": 2,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_specified": 2,
    "Familial_cold_autoinflammatory_syndrome_3|PLCG2-related_disorder": 5,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Inborn_genetic_diseases": 2,
    "Familial_cold_autoinflammatory_syndrome_3|not_provided|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 5,
    "Familial_cold_autoinflammatory_syndrome_3|PLCG2-related_disorder|not_provided": 4,
    "not_provided|not_specified|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 1,
    "Familial_cold_autoinflammatory_syndrome_3|not_provided|not_specified": 1,
    "PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3": 6,
    "PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3|not_provided": 3,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3|not_specified": 1,
    "PLCG2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Familial_cold_autoinflammatory_syndrome_3": 3,
    "Familial_cold_autoinflammatory_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_3|not_provided|Inborn_genetic_diseases": 2,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided|PLCG2-related_disorder": 1,
    "Familial_cold_autoinflammatory_syndrome_3|not_specified|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 2,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_3": 1,
    "not_provided|PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3": 3,
    "not_specified|Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 1,
    "PLCG2-related_disorder|not_provided|Familial_cold_autoinflammatory_syndrome_3": 4,
    "not_provided|PLCG2-related_disorder|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3|PLCG2-related_disorder": 1,
    "not_specified|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_provided": 1,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_specified|Familial_cold_autoinflammatory_syndrome_3|not_provided": 1,
    "not_specified|Familial_cold_autoinflammatory_syndrome_3|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_3|PLCG2-related_disorder|Inborn_genetic_diseases": 1,
    "Familial_cold_autoinflammatory_syndrome_3|PLCG2-related_disorder|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 2,
    "PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3|not_provided|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 1,
    "PLCG2-related_disorder|Clonal_Cytopenia_of_Undetermined_Significance|Familial_cold_autoinflammatory_syndrome_3": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3|Inborn_genetic_diseases": 1,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|PLCG2-related_disorder": 1,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided|not_specified": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_3|not_specified|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation": 2,
    "Familial_cold_autoinflammatory_syndrome|not_provided": 3,
    "PLCG2-related_disorder|Familial_cold_autoinflammatory_syndrome_3|Inborn_genetic_diseases": 1,
    "Familial_cold_autoinflammatory_syndrome_3|not_specified": 3,
    "Recurrent_fever|Familial_cold_autoinflammatory_syndrome_3": 1,
    "Familial_cold_autoinflammatory_syndrome_3|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_specified": 1,
    "not_specified|Familial_cold_autoinflammatory_syndrome_3": 2,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|not_provided|Familial_cold_autoinflammatory_syndrome_3|not_specified": 1,
    "not_provided|not_specified|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3": 1,
    "Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3|not_provided|PLCG2-related_disorder|Inborn_genetic_diseases": 1,
    "PLCG2-related_disorder|Autoinflammation-PLCG2-associated_antibody_deficiency-immune_dysregulation|Familial_cold_autoinflammatory_syndrome_3": 1,
    "Acromesomelic_dysplasia_4|Spondylometaphyseal_dysplasia|_pagnamenta_type": 1,
    "CDH13-related_disorder": 15,
    "CDH13-related_disorder|not_provided": 2,
    "not_provided|CDH13-related_disorder": 3,
    "Deficiency_of_malonyl-CoA_decarboxylase": 499,
    "MLYCD-related_disorder|Deficiency_of_malonyl-CoA_decarboxylase|not_provided|not_specified": 1,
    "Deficiency_of_malonyl-CoA_decarboxylase|MLYCD-related_disorder": 2,
    "Inborn_genetic_diseases|Deficiency_of_malonyl-CoA_decarboxylase": 18,
    "not_provided|Deficiency_of_malonyl-CoA_decarboxylase": 9,
    "Deficiency_of_malonyl-CoA_decarboxylase|not_specified": 8,
    "not_specified|MLYCD-related_disorder|Deficiency_of_malonyl-CoA_decarboxylase": 1,
    "Deficiency_of_malonyl-CoA_decarboxylase|not_specified|not_provided": 3,
    "Deficiency_of_malonyl-CoA_decarboxylase|not_provided": 8,
    "MLYCD-related_disorder|Deficiency_of_malonyl-CoA_decarboxylase|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Deficiency_of_malonyl-CoA_decarboxylase": 3,
    "MLYCD-related_disorder|not_specified|not_provided|Deficiency_of_malonyl-CoA_decarboxylase": 1,
    "not_specified|Deficiency_of_malonyl-CoA_decarboxylase": 9,
    "MLYCD-related_disorder|not_specified|Deficiency_of_malonyl-CoA_decarboxylase": 1,
    "Deficiency_of_malonyl-CoA_decarboxylase|not_provided|not_specified": 1,
    "MLYCD-related_disorder|Deficiency_of_malonyl-CoA_decarboxylase|not_specified": 1,
    "MLYCD-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Deficiency_of_malonyl-CoA_decarboxylase|Inborn_genetic_diseases": 1,
    "Deficiency_of_malonyl-CoA_decarboxylase|Inborn_genetic_diseases": 11,
    "not_provided|Deficiency_of_malonyl-CoA_decarboxylase|not_specified": 3,
    "not_provided|not_specified|Deficiency_of_malonyl-CoA_decarboxylase": 2,
    "MLYCD-related_disorder|Deficiency_of_malonyl-CoA_decarboxylase": 5,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_malonyl-CoA_decarboxylase": 3,
    "Deficiency_of_malonyl-CoA_decarboxylase|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "MLYCD-related_disorder|not_provided|Deficiency_of_malonyl-CoA_decarboxylase": 1,
    "not_provided|Deficiency_of_malonyl-CoA_decarboxylase|MLYCD-related_disorder": 1,
    "Inborn_genetic_diseases|Deficiency_of_malonyl-CoA_decarboxylase|not_provided": 1,
    "MLYCD-related_disorder|Deficiency_of_malonyl-CoA_decarboxylase|not_provided": 1,
    "Deficiency_of_malonyl-CoA_decarboxylase|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Deficiency_of_malonyl-CoA_decarboxylase|Inborn_genetic_diseases": 1,
    "not_specified|Deficiency_of_malonyl-CoA_decarboxylase|not_provided": 1,
    "SLC38A8-related_disorder|not_provided": 11,
    "not_provided|SLC38A8-related_disorder": 7,
    "Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome": 19,
    "FOVEAL_HYPOPLASIA_2_WITH_OPTIC_NERVE_MISROUTING": 1,
    "SLC38A8-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|FOVEAL_HYPOPLASIA_2_WITH_OPTIC_NERVE_MISROUTING_AND_ANTERIOR_SEGMENT_DYSGENESIS": 1,
    "not_provided|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome": 6,
    "Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome|not_provided": 7,
    "Foveal_hypoplasia_2_and_optic_nerve_misrouting_with_or_without_anterior_segment_dysgenesis": 1,
    "Inborn_genetic_diseases|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome": 1,
    "FOVEAL_HYPOPLASIA_2_WITH_OPTIC_NERVE_MISROUTING_AND_ANTERIOR_SEGMENT_DYSGENESIS": 1,
    "Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome|not_specified": 1,
    "not_specified|not_provided|SLC38A8-related_disorder|Inborn_genetic_diseases": 1,
    "Foveal_hypoplasia_2_and_optic_nerve_misrouting_with_or_without_anterior_segment_dysgenesis|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome|not_provided": 1,
    "not_provided|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome|Inborn_genetic_diseases": 1,
    "Foveal_hypoplasia|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome": 1,
    "SLC38A8-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome|not_specified": 1,
    "not_provided|Foveal_hypoplasia_-_optic_nerve_decussation_defect_-_anterior_segment_dysgenesis_syndrome|Foveal_hypoplasia": 1,
    "MBTPS1-related_disorder": 2,
    "Spondyloepiphyseal_dysplasia|_kondo-fu_type": 9,
    "MBTPS1-related_disorder|not_provided": 10,
    "See_cases|Spondyloepiphyseal_dysplasia|_kondo-fu_type": 1,
    "Inborn_genetic_diseases|Spondyloepiphyseal_dysplasia|_kondo-fu_type": 1,
    "not_provided|MBTPS1-related_disorder": 9,
    "not_provided|MBTPS1-related_disorder|Inborn_genetic_diseases": 1,
    "Spondyloepiphyseal_dysplasia|_kondo-fu_type|MBTPS1-related_disorder|not_provided": 2,
    "Spondyloepiphyseal_dysplasia|_kondo-fu_type|not_provided": 1,
    "Primary_ciliary_dyskinesia_13|not_provided": 1,
    "Primary_ciliary_dyskinesia_13": 26,
    "not_provided|Primary_ciliary_dyskinesia_13": 2,
    "DNAAF1-related_disorder": 2,
    "Primary_ciliary_dyskinesia_13|Primary_ciliary_dyskinesia": 27,
    "Primary_ciliary_dyskinesia|DNAAF1-related_disorder": 4,
    "DNAAF1-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13": 10,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13": 15,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13": 7,
    "Primary_ciliary_dyskinesia|DNAAF1-related_disorder|Primary_ciliary_dyskinesia_13": 2,
    "Kartagener_syndrome|Primary_ciliary_dyskinesia_13": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13": 1,
    "Primary_ciliary_dyskinesia_13|Primary_ciliary_dyskinesia|not_provided": 3,
    "DNAAF1-related_disorder|Primary_ciliary_dyskinesia_13|Primary_ciliary_dyskinesia": 2,
    "not_specified|Primary_ciliary_dyskinesia_13|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_13": 2,
    "Primary_ciliary_dyskinesia_13|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13|not_specified": 1,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Primary_ciliary_dyskinesia_13": 2,
    "not_provided|Primary_ciliary_dyskinesia_13|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_13|not_specified|Primary_ciliary_dyskinesia": 1,
    "DNAAF1-related_disorder|not_provided|Primary_ciliary_dyskinesia_13|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_13": 1,
    "Primary_ciliary_dyskinesia|Kartagener_syndrome|Primary_ciliary_dyskinesia_13": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13|not_specified": 1,
    "DNAAF1-related_disorder|not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13": 1,
    "Primary_ciliary_dyskinesia_13|Primary_ciliary_dyskinesia|DNAAF1-related_disorder|not_provided": 2,
    "DNAAF1-related_disorder|not_provided|Primary_ciliary_dyskinesia": 1,
    "DNAAF1-related_disorder|not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_13|Heterotaxy": 1,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_13|not_provided": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_13": 2,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_13|DNAAF1-related_disorder": 1,
    "Primary_ciliary_dyskinesia_13|DNAAF1-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_13|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_13": 2,
    "Thalidomide_response|not_specified|not_provided": 1,
    "TAF1C-Associated_Neurodevelopmental_Disorder": 1,
    "ATP2C2-related_disorder": 32,
    "not_provided|ATP2C2-related_disorder": 5,
    "ATP2C2-related_disorder|not_provided": 8,
    "not_specified|not_provided|ATP2C2-related_disorder": 1,
    "CRISPLD2-related_disorder": 20,
    "CRISPLD2-related_disorder|not_specified": 1,
    "not_provided|CRISPLD2-related_disorder": 8,
    "not_specified|CRISPLD2-related_disorder": 1,
    "CRISPLD2-related_disorder|not_provided": 1,
    "CIBAR2-related_disorder": 5,
    "COX4I1-related_disorder": 3,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_16": 2,
    "COX4I1-related_disorder|not_provided": 1,
    "COX4I1-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_16|not_provided": 1,
    "Immunodeficiency_32B": 4,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B|IRF8-related_disorder": 2,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 247,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B": 75,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|IRF8-related_disorder": 3,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 2,
    "IRF8-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B|not_provided": 2,
    "Inborn_genetic_diseases|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B": 6,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B": 5,
    "not_provided|Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B|not_provided": 2,
    "Inborn_genetic_diseases|Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 2,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|not_provided|not_specified": 2,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|not_provided|IRF8-related_disorder": 1,
    "not_provided|IRF8-related_disorder|Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 2,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Inborn_genetic_diseases": 5,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B|Inborn_genetic_diseases": 2,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|not_provided": 8,
    "IRF8-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B|not_provided|not_specified": 1,
    "IRF8-related_disorder|Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|not_provided": 1,
    "IRF8-related_disorder|not_provided|Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 1,
    "Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|See_cases": 1,
    "not_specified|not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency|Immunodeficiency_32B": 1,
    "Inherited_Immunodeficiency_Diseases|not_provided|Immunodeficiency_32B|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_partial_IRF8_deficiency": 1,
    "Intestinal_malrotation": 1,
    "FOXF1-related_disorder": 13,
    "FOXF1-related_disorder|not_provided": 1,
    "not_provided|FOXF1-related_disorder|Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment": 1,
    "not_provided|Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment": 7,
    "Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment|not_provided": 6,
    "Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment|Atresia_of_urethra|Fetal_megacystis|Ventricular_septal_defect": 1,
    "Inborn_genetic_diseases|FOXF1-related_disorder": 1,
    "not_provided|FOXF1-related_disorder": 3,
    "Pyloric_stenosis|_infantile_hypertrophic|_5": 1,
    "not_provided|Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment|FOXF1-related_disorder": 1,
    "Inborn_genetic_diseases|Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment": 1,
    "Alveolar_capillary_dysplasia_with_pulmonary_venous_misalignment|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Distichiasis-lymphedema_syndrome": 1,
    "Distichiasis-lymphedema_syndrome": 33,
    "FOXC2-related_disorder": 10,
    "Inborn_genetic_diseases|Distichiasis-lymphedema_syndrome|not_provided": 2,
    "Distichiasis-lymphedema_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|FOXC2-related_disorder": 2,
    "Inborn_genetic_diseases|FOXC2-related_disorder|not_provided": 1,
    "FOXC2-related_disorder|not_provided": 1,
    "not_provided|Distichiasis-lymphedema_syndrome": 1,
    "Non-immune_hydrops_fetalis|Distichiasis-lymphedema_syndrome": 1,
    "LYMPHEDEMA-DISTICHIASIS_SYNDROME_WITH_RENAL_DISEASE_AND_DIABETES_MELLITUS": 1,
    "Distichiasis-lymphedema_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Distichiasis-lymphedema_syndrome": 1,
    "Otosclerosis_11|not_provided": 1,
    "not_provided|FBXO31-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_45|not_specified": 1,
    "FBXO31-related_disorder": 5,
    "Spastic_cerebral_palsy|Intellectual_disability|_autosomal_recessive_45|not_provided|Ectopic_thyroid": 1,
    "Intellectual_disability|_autosomal_recessive_45|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_45": 4,
    "FBXO31-related_disorder|not_provided": 2,
    "not_provided|not_specified|FBXO31-related_disorder": 1,
    "not_specified|FBXO31-related_disorder": 1,
    "JPH3-related_disorder": 12,
    "JPH3-related_disorder|not_provided": 1,
    "not_provided|JPH3-related_disorder|Huntington_disease-like_2": 1,
    "Huntington_disease-like_2|Inborn_genetic_diseases": 1,
    "JPH3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|JPH3-related_disorder": 1,
    "not_provided|Huntington_disease-like_2": 1,
    "Huntington_disease-like_2": 1,
    "SLC7A5-related_disorder": 11,
    "SLC7A5-related_disorder|not_provided": 2,
    "not_provided|SLC7A5-related_disorder": 2,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 106,
    "CA5A-related_disorder": 3,
    "not_provided|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 3,
    "not_provided|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 10,
    "not_specified|not_provided|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 1,
    "not_specified|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 1,
    "CA5A-related_disorder|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided": 2,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided": 8,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided|CA5A-related_disorder": 1,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|Inborn_genetic_diseases": 5,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided|CA5A-related_disorder|not_specified": 1,
    "CA5A-related_disorder|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 5,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|CA5A-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CA5A-related_disorder|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency": 1,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_specified|not_provided": 4,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|CA5A-related_disorder": 2,
    "Inborn_genetic_diseases|Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided": 1,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_specified": 2,
    "Hyperammonemic_encephalopathy_due_to_carbonic_anhydrase_VA_deficiency|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 3,
    "not_specified|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_specified|Brittle_cornea_syndrome_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1": 41,
    "Cardiovascular_phenotype|not_provided|not_specified|Keratoconus_1": 2,
    "Cardiovascular_phenotype|not_provided|ZNF469-related_disorder|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 2,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_provided": 7,
    "Keratoconus_1|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|not_provided": 4,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 11,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|ZNF469-related_disorder|Brittle_cornea_syndrome_1": 2,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1": 5,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|Striae_distensae|Myopia|Spontaneous_hematomas|Joint_hypermobility|Gastroesophageal_reflux|Thoracic_scoliosis|Soft_skin|Poor_wound_healing": 1,
    "not_provided|Cardiovascular_phenotype|ZNF469-related_disorder|Brittle_cornea_syndrome_1": 2,
    "Cardiovascular_phenotype|ZNF469-related_disorder|not_provided": 7,
    "Cardiovascular_phenotype|not_specified|not_provided|ZNF469-related_disorder|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 1,
    "Brittle_cornea_syndrome_1|not_provided|Cardiovascular_phenotype": 21,
    "not_provided|Cardiovascular_phenotype|ZNF469-related_disorder": 9,
    "ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|not_provided": 3,
    "Cardiovascular_phenotype|ZNF469-related_disorder|not_specified|not_provided|Brittle_cornea_syndrome_1": 2,
    "Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_provided|ZNF469-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Ehlers-Danlos_syndrome": 1,
    "Brittle_cornea_syndrome_1|not_provided": 16,
    "not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 19,
    "Cardiovascular_phenotype|not_specified|not_provided|Brittle_cornea_syndrome_1": 11,
    "Cardiovascular_phenotype|not_specified|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|not_provided": 2,
    "ZNF469-related_disorder|not_provided|Cardiovascular_phenotype": 8,
    "ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype|not_provided|ZNF469-related_disorder": 1,
    "not_provided|ZNF469-related_disorder|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Brittle_cornea_syndrome_1": 9,
    "not_provided|ZNF469-related_disorder": 4,
    "not_provided|ZNF469-related_disorder|Cardiovascular_phenotype": 16,
    "Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Brittle_cornea_syndrome_1|not_provided": 4,
    "not_provided|Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome": 1,
    "not_specified|not_provided|ZNF469-related_disorder|Cardiovascular_phenotype": 1,
    "ZNF469-related_disorder|not_provided|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Keratoconus_1": 2,
    "ZNF469-related_disorder|not_provided|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1": 3,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Brittle_cornea_syndrome_1": 10,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|ZNF469-related_disorder|Brittle_cornea_syndrome_1|not_provided": 1,
    "ZNF469-related_disorder|Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|ZNF469-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|ZNF469-related_disorder|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 1,
    "not_provided|not_specified|Keratoconus_1": 1,
    "Brittle_cornea_syndrome_1|not_provided|not_specified|Ehlers-Danlos_syndrome": 1,
    "not_specified|ZNF469-related_disorder|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|ZNF469-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Brittle_cornea_syndrome_1": 4,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome": 5,
    "ZNF469-related_disorder|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Keratoconus_1|not_provided": 1,
    "Thoracic_scoliosis|Gastroesophageal_reflux|Spontaneous_hematomas|Poor_wound_healing|Myopia|Soft_skin|Striae_distensae|Joint_hypermobility|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "not_provided|not_specified|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|ZNF469-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_provided|not_specified|Ehlers-Danlos_syndrome": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "ZNF469-related_disorder": 4,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|Brittle_cornea_syndrome_1|not_provided": 2,
    "Cardiovascular_phenotype|not_provided|not_specified|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome": 1,
    "Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder|Ehlers-Danlos_syndrome": 1,
    "Keratoconus_1|not_specified": 2,
    "ZNF469-related_disorder|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder|Ehlers-Danlos_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|not_specified": 9,
    "not_provided|not_specified|Cardiovascular_phenotype|ZNF469-related_disorder": 3,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder|Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|not_specified|not_provided": 5,
    "Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Brittle_cornea_syndrome_1|not_provided|not_specified|Cardiovascular_phenotype|ZNF469-related_disorder": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Brittle_cornea_syndrome_1": 2,
    "not_provided|not_specified|Cardiovascular_phenotype|Connective_tissue_disorder": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|not_provided": 5,
    "not_provided|not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_specified|not_provided": 4,
    "Cardiovascular_phenotype|Keratoconus_1": 1,
    "Brittle_cornea_syndrome_1|ZNF469-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1": 3,
    "not_provided|ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_specified": 2,
    "Cardiovascular_phenotype|ZNF469-related_disorder|not_provided|Brittle_cornea_syndrome_1": 2,
    "Brittle_cornea_syndrome_1|ZNF469-related_disorder|not_provided|Cardiovascular_phenotype": 2,
    "Brittle_cornea_syndrome_1|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "ZNF469-related_disorder|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 1,
    "Brittle_cornea_syndrome_1|not_provided|Ehlers-Danlos_syndrome|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|ZNF469-related_disorder|not_specified|not_provided": 1,
    "not_provided|ZNF469-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|ZNF469-related_disorder|Brittle_cornea_syndrome_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|ZNF469-related_disorder": 3,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|ZNF469-related_disorder": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 5,
    "Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Brittle_cornea_syndrome_1|ZNF469-related_disorder|Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Brittle_cornea_syndrome_1|not_provided|Cardiovascular_phenotype|ZNF469-related_disorder": 1,
    "ZNF469-related_disorder|Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|not_provided|Keratoconus_1": 1,
    "Cardiovascular_phenotype|ZNF469-related_disorder|Keratoconus|not_specified|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|ZNF469-related_disorder|not_specified|not_provided": 2,
    "not_provided|ZNF469-related_disorder|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|ZNF469-related_disorder|Ehlers-Danlos_syndrome": 2,
    "ZNF469-related_disorder|not_provided|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_specified|Brittle_cornea_syndrome_1": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1": 6,
    "not_provided|Cardiovascular_phenotype|not_specified|Keratoconus_1": 1,
    "ZNF469-related_disorder|not_provided": 2,
    "not_specified|not_provided|Brittle_cornea_syndrome_1": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|ZNF469-related_disorder|Brittle_cornea_syndrome_1": 1,
    "Brittle_cornea_syndrome_1|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 1,
    "not_specified|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|Brittle_cornea_syndrome_1": 2,
    "not_specified|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_provided": 4,
    "Ehlers-Danlos_syndrome|not_specified|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|ZNF469-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1|ZNF469-related_disorder": 1,
    "Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 2,
    "ZNF469-related_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 3,
    "Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome|ZNF469-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_provided|not_specified": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|not_specified|not_provided": 1,
    "Thoracic_scoliosis|Gastroesophageal_reflux|Spontaneous_hematomas|Poor_wound_healing|Myopia|Soft_skin|Striae_distensae|Joint_hypermobility|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|not_specified": 1,
    "Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 3,
    "Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|ZNF469-related_disorder": 1,
    "Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_specified|not_provided|Ehlers-Danlos_syndrome": 1,
    "not_specified|Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|ZNF469-related_disorder": 1,
    "not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1|Cardiovascular_phenotype": 1,
    "Keratoconus_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Ehlers-Danlos_syndrome|Brittle_cornea_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|ZNF469-related_disorder|Ehlers-Danlos_syndrome": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Ehlers-Danlos_syndrome|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Brittle_cornea_syndrome_1|Ehlers-Danlos_syndrome": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|Brittle_cornea_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|not_specified|Brittle_cornea_syndrome_1": 1,
    "Cardiovascular_phenotype|ZNF469-related_disorder|Brittle_cornea_syndrome_1|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|ZNF469-related_disorder|not_provided|Keratoconus_1|Brittle_cornea_syndrome_1": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Brittle_cornea_syndrome_1|ZNF469-related_disorder": 1,
    "ZNF469-related_disorder|not_provided|Cardiovascular_phenotype|Brittle_cornea_syndrome_1": 1,
    "ZNF469-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|Brittle_cornea_syndrome|Brittle_cornea_syndrome_1|not_provided": 1,
    "Ehlers-Danlos_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|ZNF469-related_disorder|not_provided": 1,
    "not_specified|Brittle_cornea_syndrome_1": 1,
    "Brittle_cornea_syndrome_1|not_specified|not_provided": 1,
    "not_specified|Congenital_heart_defect": 1,
    "not_specified|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 3,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_specified": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 329,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Chronic_granulomatous_disease": 18,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Granulomatous_disease|_chronic|_X-linked": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 24,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Inborn_genetic_diseases": 4,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|CYBA-related_disorder": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Inborn_genetic_diseases|not_provided": 2,
    "CYBA-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided": 1,
    "Inborn_genetic_diseases|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 2,
    "Chronic_granulomatous_disease|not_specified|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 1,
    "CYBA-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 2,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided|Chronic_granulomatous_disease": 2,
    "Chronic_granulomatous_disease|Inborn_genetic_diseases|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 2,
    "Chronic_granulomatous_disease|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 3,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 2,
    "Inborn_genetic_diseases|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Chronic_granulomatous_disease": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided|CYBA-related_disorder|not_specified": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 7,
    "not_provided|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_specified": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Chronic_granulomatous_disease|Polyglandular_autoimmune_syndrome|_type_1|not_provided": 1,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Chronic_granulomatous_disease": 1,
    "CYBA-related_disorder": 1,
    "CYBA-related_disorder|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 1,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 5,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|CYBA-related_disorder": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided": 1,
    "Very_early_onset_inflammatory_bowel_disease|not_specified|not_provided|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|CYBA_POLYMORPHISM": 1,
    "See_cases|not_specified|not_provided|CYBA-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided|Chronic_granulomatous_disease|not_specified": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_specified": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Inborn_genetic_diseases|Chronic_granulomatous_disease": 2,
    "CYBA-related_disorder|not_provided|not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Inborn_genetic_diseases": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Chronic_granulomatous_disease|not_provided": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_provided|Chronic_granulomatous_disease": 1,
    "CYBA-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|Chronic_granulomatous_disease": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-negative|not_specified|not_provided|Chronic_granulomatous_disease": 1,
    "Nonsyndromic_hearing_impairment": 3,
    "Porokeratosis_7|_multiple_types": 9,
    "MVD-related_disorder": 6,
    "Porokeratosis_7|_multiple_types|MVD-related_disorder": 1,
    "not_specified|Porokeratosis_7|_multiple_types": 1,
    "not_specified|MVD-related_disorder": 1,
    "MVD-related_disorder|not_provided": 1,
    "not_provided|Porokeratosis_7|_multiple_types|MVD-related_disorder": 1,
    "Porokeratosis_7|_multiple_types|MVD-related_disorder|Linear_porokeratosis|not_provided": 1,
    "CTU2-related_disorder": 15,
    "CTU2-related_disorder|not_provided": 15,
    "not_provided|Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome": 6,
    "CTU2-related_disorder|Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome|not_provided": 2,
    "not_provided|not_specified|Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome": 1,
    "Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome": 9,
    "Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome|not_provided": 4,
    "not_provided|not_specified|CTU2-related_disorder": 1,
    "not_provided|CTU2-related_disorder": 10,
    "not_specified|CTU2-related_disorder|not_provided|Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome": 1,
    "not_provided|Microcephaly|Microcephaly|_facial_dysmorphism|_renal_agenesis|_and_ambiguous_genitalia_syndrome": 1,
    "not_specified|CTU2-related_disorder": 1,
    "not_specified|not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "CTU2-related_disorder|not_specified": 1,
    "Lymphatic_malformation_6": 50,
    "Inborn_genetic_diseases|not_provided|Lymphatic_malformation_6": 3,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 20,
    "PIEZO1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Lymphatic_malformation_6": 3,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6": 12,
    "Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided": 10,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|Blood_group|_ER|not_provided|PIEZO1-related_disorder": 1,
    "PIEZO1-related_disorder|not_provided": 58,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|not_provided": 3,
    "not_specified|PIEZO1-related_disorder|not_provided": 3,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided": 3,
    "not_provided|PIEZO1-related_disorder": 71,
    "Lymphatic_malformation_6|not_provided": 14,
    "PIEZO1-related_disorder": 100,
    "See_cases|not_provided|PIEZO1-related_disorder": 1,
    "PIEZO1-related_disorder|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|Blood_group|_ER|not_provided|Non-immune_hydrops_fetalis": 1,
    "PIEZO1-related_disorder|not_provided|Inborn_genetic_diseases": 5,
    "Lymphatic_malformation_6|not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 19,
    "Inborn_genetic_diseases|PIEZO1-related_disorder": 3,
    "not_provided|PIEZO1-related_disorder|Inborn_genetic_diseases": 6,
    "not_provided|Blood_group|_ER|Inborn_genetic_diseases": 1,
    "Blood_group|_ER|not_provided": 2,
    "not_provided|Hydrops_fetalis": 1,
    "not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6": 15,
    "PIEZO1-related_disorder|Blood_group|_ER|not_provided": 1,
    "Blood_group|_ER|ER_BLOOD_GROUP_SYSTEM|_ER(a-b-)|PIEZO1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|PIEZO1-related_disorder": 7,
    "not_provided|Lymphatic_malformation_6": 8,
    "Lymphatic_malformation_6|Inborn_genetic_diseases": 2,
    "Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Blood_group|_ER": 2,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|PIEZO1-related_disorder|not_provided": 1,
    "Lymphatic_malformation_6|Inborn_genetic_diseases|not_provided": 5,
    "Lymphatic_malformation_6|PIEZO1-related_disorder|Non-immune_hydrops_fetalis": 1,
    "not_specified|not_provided|PIEZO1-related_disorder": 1,
    "PIEZO1-related_disorder|Inborn_genetic_diseases|not_provided": 9,
    "not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 11,
    "not_provided|PIEZO1-related_disorder|Lymphatic_malformation_6": 1,
    "Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided|PIEZO1-related_disorder": 1,
    "Hydrops_fetalis|Polyhydramnios": 1,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|not_provided|PIEZO1-related_disorder": 2,
    "not_provided|not_specified|PIEZO1-related_disorder": 3,
    "Inborn_genetic_diseases|Lymphatic_malformation_6|not_specified|not_provided": 1,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|PIEZO1-related_disorder": 1,
    "Inborn_genetic_diseases|Lymphatic_malformation_6|not_provided": 5,
    "Inborn_genetic_diseases|PIEZO1-related_disorder|not_provided": 7,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided|Inborn_genetic_diseases|PIEZO1-related_disorder": 1,
    "not_provided|Lymphatic_malformation_6|Inborn_genetic_diseases": 4,
    "PIEZO1-related_disorder|Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|PIEZO1-related_disorder": 3,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided|Lymphatic_malformation_6|ER_BLOOD_GROUP_SYSTEM|_ER(a-b-)|PIEZO1-related_disorder": 1,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Lymphatic_malformation_6": 3,
    "Diffuse_lymphatic_malformation": 1,
    "PIEZO1-related_disorder|Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|PIEZO1-related_disorder": 1,
    "Lymphatic_malformation_6|not_provided|not_specified|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 1,
    "Hydrops_fetalis|Polyhydramnios|Thickened_nuchal_skin_fold|not_provided": 1,
    "Thickened_nuchal_skin_fold|Hydrops_fetalis": 2,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|PIEZO1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 2,
    "Thickened_nuchal_skin_fold|Hydrops_fetalis|Polyhydramnios": 1,
    "not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|PIEZO1-related_disorder": 1,
    "not_provided|Blood_group|_ER|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|PIEZO1-related_disorder": 1,
    "PIEZO1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided": 1,
    "PIEZO1-related_disorder|Lymphatic_malformation_6": 1,
    "PIEZO1-related_disorder|Lymphatic_malformation_6|not_provided": 1,
    "PIEZO1-related_disorder|not_provided|Lymphatic_malformation_6": 1,
    "Inborn_genetic_diseases|not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6": 1,
    "not_provided|Hydrops_fetalis|PIEZO1-related_disorder": 1,
    "Lymphatic_malformation_6|PIEZO1-related_disorder|not_provided": 1,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Lymphatic_malformation_6|Inborn_genetic_diseases|not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 1,
    "not_provided|not_specified|Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 1,
    "Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_provided|Inborn_genetic_diseases": 2,
    "Lymphatic_malformation_6|PIEZO1-related_disorder|not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_specified": 1,
    "not_provided|Non-immune_hydrops_fetalis|Pancytopenia": 1,
    "Inborn_genetic_diseases|PIEZO1-related_disorder|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Lymphatic_malformation_6": 1,
    "not_provided|PIEZO1-related_disorder|not_specified": 1,
    "not_specified|PIEZO1-related_disorder|Lymphatic_malformation_6|not_provided": 1,
    "not_specified|not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 1,
    "Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|not_specified|not_provided": 1,
    "not_specified|PIEZO1-related_disorder": 1,
    "Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema|Blood_group|_ER|not_provided": 1,
    "PIEZO1-related_disorder|Inborn_genetic_diseases": 2,
    "Lymphatic_malformation_6|Inborn_genetic_diseases|PIEZO1-related_disorder": 1,
    "not_provided|Lymphatic_malformation_6|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 2,
    "Inborn_genetic_diseases|PIEZO1-related_disorder|not_provided|Dehydrated_hereditary_stomatocytosis_with_or_without_pseudohyperkalemia_and/or_perinatal_edema": 1,
    "PIEZO1-related_disorder|not_provided|not_specified": 1,
    "Lymphatic_malformation_6|PIEZO1-related_disorder|not_specified|not_provided": 1,
    "PIEZO1-related_disorder|Inborn_genetic_diseases|Lymphatic_malformation_6": 1,
    "Meier-Gorlin_syndrome_4": 13,
    "Meier-Gorlin_syndrome_4|not_provided": 3,
    "not_provided|CDT1-related_disorder|not_specified": 3,
    "CDT1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CDT1-related_disorder": 2,
    "Meier-Gorlin_syndrome_4|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CDT1-related_disorder|Meier-Gorlin_syndrome_4": 1,
    "not_specified|not_provided|Meier-Gorlin_syndrome_4": 3,
    "CDT1-related_disorder|not_provided": 5,
    "not_provided|Meier-Gorlin_syndrome_4|not_specified": 1,
    "not_provided|Meier-Gorlin_syndrome_4": 3,
    "Inborn_genetic_diseases|not_provided|CDT1-related_disorder": 1,
    "CDT1-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|CDT1-related_disorder": 1,
    "CDT1-related_disorder": 1,
    "Meier-Gorlin_syndrome_4|not_provided|Meier-Gorlin_syndrome": 1,
    "CDT1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Meier-Gorlin_syndrome_4": 1,
    "Adenine_phosphoribosyltransferase_deficiency|not_specified|not_provided": 1,
    "Meier-Gorlin_syndrome_4|not_provided|not_specified": 1,
    "Adenine_phosphoribosyltransferase_deficiency": 92,
    "Adenine_phosphoribosyltransferase_deficiency|Morquio_syndrome": 1,
    "not_provided|Adenine_phosphoribosyltransferase_deficiency|Morquio_syndrome": 3,
    "not_provided|Adenine_phosphoribosyltransferase_deficiency|See_cases": 1,
    "Adenine_phosphoribosyltransferase_deficiency|APRT-related_disorder": 1,
    "Inborn_genetic_diseases|Adenine_phosphoribosyltransferase_deficiency|not_provided": 1,
    "Adenine_phosphoribosyltransferase_deficiency|not_provided": 5,
    "not_provided|Adenine_phosphoribosyltransferase_deficiency": 13,
    "Inborn_genetic_diseases|Adenine_phosphoribosyltransferase_deficiency": 3,
    "Adenine_phosphoribosyltransferase_deficiency|APRT_deficiency|_Japanese_type": 1,
    "not_provided|APRT-related_disorder": 1,
    "APRT-related_disorder|not_provided|Adenine_phosphoribosyltransferase_deficiency": 1,
    "APRT-related_disorder|not_provided": 1,
    "not_provided|Adenine_phosphoribosyltransferase_deficiency|Inborn_genetic_diseases": 1,
    "Adenine_phosphoribosyltransferase_deficiency|not_provided|Morquio_syndrome": 3,
    "Adenine_phosphoribosyltransferase_deficiency|not_provided|Mucopolysaccharidosis|_MPS-IV-A|Morquio_syndrome": 5,
    "Mucopolysaccharidosis|_MPS-IV-A": 949,
    "Adenine_phosphoribosyltransferase_deficiency|Mucopolysaccharidosis|_MPS-IV-A|not_provided|Morquio_syndrome": 2,
    "Mucopolysaccharidosis|_MPS-IV-A|Morquio_syndrome": 12,
    "not_provided|Morquio_syndrome|Mucopolysaccharidosis|_MPS-IV-A": 2,
    "Mucopolysaccharidosis|_MPS-IV-A|not_provided|Adenine_phosphoribosyltransferase_deficiency": 1,
    "Morquio_syndrome": 2,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-A": 34,
    "Morquio_syndrome|Adenine_phosphoribosyltransferase_deficiency|Mucopolysaccharidosis|_MPS-IV-A|not_specified|not_provided": 1,
    "Morquio_syndrome|not_provided|Mucopolysaccharidosis|_MPS-IV-A": 9,
    "Mucopolysaccharidosis|_MPS-IV-A|not_provided": 19,
    "GALNS-related_disorder|Mucopolysaccharidosis|_MPS-IV-A": 4,
    "not_specified|Mucopolysaccharidosis|_MPS-IV-A": 27,
    "not_specified|Mucopolysaccharidosis|_MPS-IV-A|not_provided": 8,
    "Morquio_syndrome|Mucopolysaccharidosis|_MPS-IV-A": 25,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-IV-A": 5,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-A|not_specified": 7,
    "Mucopolysaccharidosis|_MPS-IV-A|not_specified": 8,
    "GALNS-related_disorder": 7,
    "not_specified|not_provided|Mucopolysaccharidosis|_MPS-IV-A": 8,
    "Mucopolysaccharidosis|_MPS-IV-A|not_specified|not_provided": 4,
    "not_provided|not_specified|Mucopolysaccharidosis|_MPS-IV-A": 4,
    "not_specified|not_provided|GALNS-related_disorder|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-A|GALNS-related_disorder": 2,
    "Mucopolysaccharidosis|_MPS-IV-A|not_provided|Morquio_syndrome": 3,
    "Mucopolysaccharidosis|_MPS-IV-A|not_specified|not_provided|Morquio_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-IV-A|not_specified|GALNS-related_disorder": 2,
    "not_provided|GALNS-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-IV-A|GALNS-related_disorder": 4,
    "Mucopolysaccharidosis|_MPS-IV-A|Morquio_syndrome|not_provided": 3,
    "Morquio_syndrome|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "Mucopolysaccharidosis|_MPS-IV-A|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Morquio_syndrome|not_provided|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "Abnormality_of_metabolism/homeostasis|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-A|Morquio_syndrome": 4,
    "Mucopolysaccharidosis|_MPS-IV-A|not_provided|not_specified": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-IV-A|Skeletal_dysplasia": 1,
    "Morquio_syndrome|Mucopolysaccharidosis|_MPS-IV-A|not_provided": 2,
    "not_provided|Morquio_syndrome|Mucopolysaccharidosis|_MPS-IV-A|Inborn_genetic_diseases": 1,
    "not_provided|Skeletal_dysplasia|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "not_provided|GALNS-related_disorder|Mucopolysaccharidosis|_MPS-IV-A": 2,
    "GALNS-related_disorder|Mucopolysaccharidosis|_MPS-IV-A|Morquio_syndrome": 1,
    "Mucopolysaccharidosis|_MPS-IV-A|Inborn_genetic_diseases|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-IV-A|Morquio_syndrome|GALNS-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|GALNS-related_disorder|Morquio_syndrome|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "Inborn_genetic_diseases|Morquio_syndrome|Mucopolysaccharidosis|_MPS-IV-A": 1,
    "GALNS-related_disorder|not_provided": 1,
    "Intellectual_disability|Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis": 1,
    "TRAPPC2L-related_disorder|Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis": 1,
    "Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis": 7,
    "TRAPPC2L-related_disorder": 11,
    "Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis|not_specified": 2,
    "Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis|TRAPPC2L-related_disorder|not_provided": 1,
    "TRAPPC2L-related_disorder|not_provided": 1,
    "not_provided|Combined_malonic_and_methylmalonic_acidemia": 24,
    "Combined_malonic_and_methylmalonic_acidemia|Methylmalonic_acidemia": 13,
    "ACSF3-related_disorder|not_provided|Combined_malonic_and_methylmalonic_acidemia": 2,
    "Combined_malonic_and_methylmalonic_acidemia|not_provided|not_specified|Methylmalonic_acidemia": 2,
    "Combined_malonic_and_methylmalonic_acidemia": 696,
    "not_specified|not_provided|Combined_malonic_and_methylmalonic_acidemia": 3,
    "Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia": 12,
    "Combined_malonic_and_methylmalonic_acidemia|Global_developmental_delay": 1,
    "Combined_malonic_and_methylmalonic_acidemia|not_provided": 14,
    "Combined_malonic_and_methylmalonic_acidemia|Methylmalonic_acidemia|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia": 11,
    "not_provided|Combined_malonic_and_methylmalonic_acidemia|not_specified|Methylmalonic_acidemia": 2,
    "Combined_malonic_and_methylmalonic_acidemia|not_specified": 8,
    "ACSF3-related_disorder|Combined_malonic_and_methylmalonic_acidemia": 7,
    "Combined_malonic_and_methylmalonic_acidemia|Inborn_genetic_diseases|not_provided": 1,
    "Combined_malonic_and_methylmalonic_acidemia|Inborn_genetic_diseases": 6,
    "Combined_malonic_and_methylmalonic_acidemia|Methylmalonic_acidemia|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Methylmalonic_acidemia": 1,
    "Combined_malonic_and_methylmalonic_acidemia|ACSF3-related_disorder": 9,
    "Combined_malonic_and_methylmalonic_acidemia|Methylmalonic_acidemia|not_provided": 1,
    "Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia|Methylmalonic_acidemia": 2,
    "ACSF3-related_disorder": 3,
    "Inborn_genetic_diseases|Methylmalonic_acidemia": 2,
    "not_specified|Combined_malonic_and_methylmalonic_acidemia|not_provided": 2,
    "Combined_malonic_and_methylmalonic_acidemia|not_provided|not_specified": 2,
    "not_specified|Combined_malonic_and_methylmalonic_acidemia": 15,
    "Methylmalonic_acidemia|not_provided|Combined_malonic_and_methylmalonic_acidemia": 2,
    "Methylmalonic_acidemia|Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Combined_malonic_and_methylmalonic_acidemia|not_specified|not_provided|Methylmalonic_acidemia": 2,
    "Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia|not_provided|not_specified": 1,
    "Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia|not_provided": 1,
    "not_specified|Combined_malonic_and_methylmalonic_acidemia|not_provided|Methylmalonic_acidemia": 1,
    "not_provided|Combined_malonic_and_methylmalonic_acidemia|Inborn_genetic_diseases": 1,
    "ACSF3-related_disorder|not_specified|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia|not_provided|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Combined_malonic_and_methylmalonic_acidemia|not_specified|not_provided": 3,
    "not_provided|Combined_malonic_and_methylmalonic_acidemia|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Combined_malonic_and_methylmalonic_acidemia|Inborn_genetic_diseases|Methylmalonic_acidemia|not_provided": 1,
    "not_provided|not_specified|Combined_malonic_and_methylmalonic_acidemia": 2,
    "not_provided|Inborn_genetic_diseases|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia|not_specified": 1,
    "ACSF3-related_disorder|not_provided|not_specified|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Combined_malonic_and_methylmalonic_acidemia|Methylmalonic_acidemia|not_provided|not_specified": 1,
    "not_provided|Combined_malonic_and_methylmalonic_acidemia|ACSF3-related_disorder": 1,
    "ACSF3-related_disorder|Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia|not_provided|Methylmalonic_acidemia": 1,
    "not_provided|not_specified|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Combined_malonic_and_methylmalonic_acidemia|ACSF3-related_disorder|not_specified": 1,
    "not_provided|ACSF3-related_disorder|Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia|Inborn_genetic_diseases": 1,
    "not_specified|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia|not_provided": 1,
    "Inborn_genetic_diseases|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia|not_provided": 1,
    "Combined_malonic_and_methylmalonic_acidemia|Inborn_genetic_diseases|Methylmalonic_acidemia": 1,
    "ACSF3-related_disorder|Inborn_genetic_diseases|not_provided|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Inborn_genetic_diseases|not_provided|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia": 1,
    "ACSF3-related_disorder|Combined_malonic_and_methylmalonic_acidemia|not_provided": 1,
    "ACSF3-related_disorder|Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Combined_malonic_and_methylmalonic_acidemia": 1,
    "ACSF3-related_disorder|Combined_malonic_and_methylmalonic_acidemia|not_specified": 1,
    "Inborn_genetic_diseases|Combined_malonic_and_methylmalonic_acidemia|not_specified": 1,
    "not_specified|Methylmalonic_acidemia|Combined_malonic_and_methylmalonic_acidemia": 1,
    "Methylmalonic_acidemia|ACSF3-related_disorder": 2,
    "not_specified|Intellectual_disability|_autosomal_dominant_3": 1,
    "not_specified|CDH15-related_disorder": 1,
    "not_provided|CDH15-related_disorder": 3,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_3": 3,
    "Intellectual_disability|_autosomal_dominant_3|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_3": 18,
    "Intellectual_disability|_autosomal_dominant_3|not_specified": 2,
    "CDH15-related_disorder": 15,
    "Intellectual_disability|_autosomal_dominant_3|not_provided|CDH15-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_3|not_specified": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Intellectual_disability": 1,
    "not_provided|not_specified|Intellectual_disability|_autosomal_dominant_3": 1,
    "CDH15-related_disorder|not_provided": 2,
    "CDH15-related_disorder|Intellectual_disability|not_specified": 1,
    "CDH15-related_disorder|not_provided|not_specified": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_3|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_3|Intellectual_disability": 1,
    "Intellectual_disability|not_provided|not_specified": 3,
    "Obesity|Global_developmental_delay|Seizure|Microcephaly": 1,
    "not_provided|KBG_syndrome": 130,
    "Inborn_genetic_diseases|KBG_syndrome": 91,
    "KBG_syndrome|Inborn_genetic_diseases": 82,
    "KBG_syndrome|not_provided": 95,
    "ANKRD11-related_disorder": 57,
    "not_provided|Inborn_genetic_diseases|KBG_syndrome": 14,
    "KBG_syndrome|not_provided|Inborn_genetic_diseases": 19,
    "KBG_syndrome|Intellectual_disability|not_provided|ANKRD11-related_disorder": 1,
    "KBG_syndrome|ANKRD11-related_disorder|not_provided": 2,
    "not_provided|KBG_syndrome|Inborn_genetic_diseases": 15,
    "KBG_syndrome|Inborn_genetic_diseases|ANKRD11-related_disorder": 3,
    "Inborn_genetic_diseases|ANKRD11-related_disorder|not_provided|KBG_syndrome": 6,
    "ANKRD11-related_disorder|KBG_syndrome": 13,
    "Inborn_genetic_diseases|KBG_syndrome|not_provided": 24,
    "Inborn_genetic_diseases|not_provided|KBG_syndrome": 33,
    "KBG_syndrome|Inborn_genetic_diseases|not_provided|ANKRD11-related_disorder|not_specified": 1,
    "KBG_syndrome|not_provided|ANKRD11-related_disorder": 4,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|KBG_syndrome": 3,
    "not_provided|KBG_syndrome|ANKRD11-related_disorder|not_specified": 2,
    "KBG_syndrome|Inborn_genetic_diseases|not_provided": 18,
    "not_provided|See_cases|KBG_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|KBG_syndrome|Sudden_unexplained_death_in_childhood": 1,
    "KBG_syndrome|ANKRD11-related_disorder": 12,
    "KBG_syndrome|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "ANKRD11-related_disorder|not_provided|KBG_syndrome": 6,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|not_provided|KBG_syndrome": 5,
    "KBG_syndrome|not_specified": 9,
    "KBG_syndrome|Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis": 1,
    "not_specified|Inborn_genetic_diseases|See_cases": 1,
    "Inborn_genetic_diseases|ANKRD11-related_disorder|KBG_syndrome": 3,
    "KBG_syndrome|Inborn_genetic_diseases|not_provided|ANKRD11-related_disorder": 2,
    "not_provided|Intellectual_disability|KBG_syndrome": 1,
    "KBG_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "not_provided|ANKRD11-related_disorder|KBG_syndrome|Inborn_genetic_diseases": 3,
    "KBG_syndrome|ANKRD11-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "KBG_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|not_provided|KBG_syndrome|Atypical_behavior|Seizure|Hand_tremor|Global_developmental_delay|Macrocephaly": 1,
    "Inborn_genetic_diseases|KBG_syndrome|ANKRD11-related_disorder": 6,
    "Inborn_genetic_diseases|ANKRD11-related_disorder|KBG_syndrome|not_provided": 3,
    "Intellectual_disability|KBG_syndrome": 4,
    "KBG_syndrome|ANKRD11-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "ANKRD11-related_disorder|KBG_syndrome|Inborn_genetic_diseases": 4,
    "ANKRD11-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|KBG_syndrome": 1,
    "Rare_genetic_intellectual_disability|Inborn_genetic_diseases|not_provided|KBG_syndrome|Epilepsy": 1,
    "Inborn_genetic_diseases|not_provided|KBG_syndrome|not_specified": 2,
    "ANKRD11-related_disorder|KBG_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|not_provided|Inborn_genetic_diseases|KBG_syndrome": 1,
    "ANKRD11-related_disorder|KBG_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|KBG_syndrome|ANKRD11-related_disorder|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|ANKRD11-related_disorder|KBG_syndrome": 2,
    "KBG_syndrome|not_specified|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|ANKRD11-related_disorder": 4,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|ANKRD11-related_disorder|Inborn_genetic_diseases|KBG_syndrome": 4,
    "Neurodevelopmental_abnormality|Decreased_total_neutrophil_count": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|KBG_syndrome": 3,
    "not_specified|Inborn_genetic_diseases|not_provided|KBG_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|KBG_syndrome|ANKRD11-related_disorder": 5,
    "not_provided|Inborn_genetic_diseases|KBG_syndrome|ANKRD11-related_disorder": 2,
    "KBG_syndrome|Moderate_intellectual_deficiency": 1,
    "not_specified|KBG_syndrome": 12,
    "not_specified|KBG_syndrome|Inborn_genetic_diseases": 2,
    "ANKRD11-related_disorder|not_provided": 1,
    "ANKRD11-related_disorder|not_provided|Inborn_genetic_diseases|KBG_syndrome": 2,
    "KBG_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Intellectual_disability|not_provided|Inborn_genetic_diseases|KBG_syndrome": 1,
    "KBG_syndrome|not_provided|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|KBG_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|KBG_syndrome|Intellectual_disability|not_provided": 2,
    "not_specified|not_provided|KBG_syndrome": 3,
    "Inborn_genetic_diseases|KBG_syndrome|not_provided|Intellectual_disability": 1,
    "ANKRD11-related_disorder|KBG_syndrome|not_specified": 1,
    "not_specified|Intellectual_disability|ANKRD11-related_disorder|KBG_syndrome|not_provided|Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis|Inborn_genetic_diseases": 1,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|KBG_syndrome|not_provided|Vascular_disorder": 1,
    "KBG_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "ANKRD11-related_disorder|KBG_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "KBG_syndrome|See_cases": 1,
    "not_provided|KBG_syndrome|ANKRD11-related_disorder": 1,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|KBG_syndrome": 1,
    "Astigmatism|Cryptorchidism|Intellectual_disability|Wide_nasal_bridge|Hypermetropia|Retrognathia|Esotropia|Hypertelorism|Epicanthus|Global_developmental_delay": 1,
    "ANKRD11-related_disorder|KBG_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "ANKRD11-related_disorder|not_specified|not_provided|KBG_syndrome|Inborn_genetic_diseases": 1,
    "KBG_syndrome|ANKRD11-related_disorder|Inborn_genetic_diseases": 1,
    "KBG_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 3,
    "KBG_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|KBG_syndrome": 1,
    "KBG_syndrome|Seizure": 1,
    "Inborn_genetic_diseases|not_provided|KBG_syndrome|See_cases|Intellectual_disability": 1,
    "not_specified|not_provided|KBG_syndrome|ANKRD11-related_disorder|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|KBG_syndrome|ANKRD11-related_disorder": 1,
    "not_provided|KBG_syndrome|Intellectual_disability": 1,
    "ANKRD11-related_disorder|not_provided|KBG_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "KBG_syndrome|not_provided|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|KBG_syndrome|ANKRD11-related_disorder|not_provided": 2,
    "not_provided|KBG_syndrome|Inborn_genetic_diseases|not_specified": 3,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|not_specified|KBG_syndrome|not_provided": 1,
    "KBG_syndrome|Inborn_genetic_diseases|Rare_genetic_intellectual_disability|not_provided": 1,
    "ANKRD11-related_disorder|KBG_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|KBG_syndrome|not_provided": 1,
    "not_provided|KBG_syndrome|Multiple_congenital_anomalies/dysmorphic_syndrome": 1,
    "not_provided|KBG_syndrome|Inborn_genetic_diseases|not_specified|ANKRD11-related_disorder": 1,
    "not_provided|ANKRD11-related_disorder": 1,
    "Rare_genetic_intellectual_disability|not_provided|KBG_syndrome": 1,
    "not_provided|KBG_syndrome|ANKRD11-related_disorder|Abnormality_of_the_nervous_system": 1,
    "KBG_syndrome|ANKRD11-related_disorder|not_specified": 1,
    "KBG_syndrome|ANKRD11-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|not_provided|KBG_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|KBG_syndrome|Developmental_disorder": 1,
    "not_specified|KBG_syndrome|not_provided": 1,
    "ANKRD11-related_disorder|not_provided|Global_developmental_delay|KBG_syndrome": 1,
    "ANKRD11-related_disorder|not_specified|KBG_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "KBG_syndrome|Global_developmental_delay|Inborn_genetic_diseases|ANKRD11-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Rare_genetic_intellectual_disability|Global_developmental_delay|KBG_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|KBG_syndrome": 1,
    "not_specified|not_provided|KBG_syndrome|Inborn_genetic_diseases|ANKRD11-related_disorder": 1,
    "KBG_syndrome|not_specified|Inborn_genetic_diseases|ANKRD11-related_disorder": 1,
    "KBG_syndrome|Developmental_disorder": 1,
    "not_provided|Global_developmental_delay": 3,
    "Delayed_speech_and_language_development|Seizure|Global_developmental_delay|Abnormal_facial_shape|Conductive_hearing_impairment|ANKRD11-related_disorder|Inborn_genetic_diseases|Rare_genetic_intellectual_disability|not_provided|KBG_syndrome|Neurodevelopmental_delay|Intellectual_disability|Unilateral_cryptorchidism|Short_palm|Ptosis|Short_foot|Clinodactyly_of_the_5th_finger": 1,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|KBG_syndrome|not_specified": 1,
    "not_provided|KBG_syndrome|not_specified": 2,
    "not_specified|Inborn_genetic_diseases|KBG_syndrome": 1,
    "not_provided|ANKRD11-related_disorder|KBG_syndrome": 1,
    "Global_developmental_delay|KBG_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|KBG_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "ANKRD11-related_disorder|Inborn_genetic_diseases|KBG_syndrome|not_provided": 1,
    "ANKRD11-related_disorder|not_specified|KBG_syndrome": 1,
    "not_provided|ANKRD11-related_disorder|KBG_syndrome|Inborn_genetic_diseases|Encephalopathy|_progressive|_early-onset|_with_episodic_rhabdomyolysis": 1,
    "Inborn_genetic_diseases|KBG_syndrome|not_provided|ANKRD11-related_disorder": 1,
    "SPG7-related_disorder|not_provided|Hereditary_spastic_paraplegia_7": 3,
    "Hereditary_spastic_paraplegia_7|not_provided": 52,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_7|Optic_atrophy|Retinal_dystrophy": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|not_specified": 4,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_7": 10,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_7": 7,
    "not_provided|Hereditary_spastic_paraplegia_7": 50,
    "Hereditary_spastic_paraplegia_7|Inborn_genetic_diseases": 14,
    "Hereditary_spastic_paraplegia_7|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|SPG7-related_disorder": 3,
    "Hereditary_spastic_paraplegia_7|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Hereditary_spastic_paraplegia_7|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_7|Polyneuropathy": 1,
    "Hereditary_spastic_paraplegia_7|SPG7-related_disorder": 3,
    "not_specified|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_7": 4,
    "Hereditary_spastic_paraplegia_7|not_specified": 13,
    "SPG7-related_disorder|not_provided": 2,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 6,
    "not_provided|Hereditary_spastic_paraplegia_7|not_specified|Hereditary_spastic_paraplegia": 1,
    "Proximal_spinal_muscular_atrophy|SPG7-related_disorder|Hereditary_ataxia|Retinal_dystrophy|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_7|not_specified": 1,
    "Hereditary_spastic_paraplegia_7|Hereditary_spastic_paraplegia": 5,
    "Hereditary_spastic_paraplegia_7|Hereditary_spastic_paraplegia|not_provided|SPG7-related_disorder": 1,
    "SPG7-related_disorder": 8,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|Hereditary_spastic_paraplegia|not_provided": 2,
    "Hereditary_spastic_paraplegia_7|not_provided|Early-onset_progressive_neurodegeneration-blindness-ataxia-spasticity_syndrome": 1,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_7": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_7": 8,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 6,
    "Retinal_dystrophy|SPG7-related_disorder|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "SPG7-related_disorder|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|not_provided": 1,
    "Hereditary_spastic_paraplegia_7|not_provided|Optic_atrophy|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Hereditary_spastic_paraplegia_7": 1,
    "not_specified|Hereditary_spastic_paraplegia_7|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|SPG7-related_disorder|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Inborn_genetic_diseases|SPG7-related_disorder|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Spastic_ataxia|Hereditary_spastic_paraplegia_7|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_7|Mitochondrial_disease": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_7": 8,
    "Hereditary_spastic_paraplegia_7|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|not_provided|SPG7-related_disorder": 1,
    "SPG7-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|not_provided|SPG7-related_disorder|Hereditary_spastic_paraplegia": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_1|Retinal_dystrophy|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|SPG7-related_disorder|not_provided|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 6,
    "not_provided|SPG7-related_disorder|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|Inborn_genetic_diseases|not_provided": 2,
    "SPG7-related_disorder|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|not_specified|not_provided": 2,
    "Retinal_dystrophy|not_specified|Hereditary_spastic_paraplegia_7|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_7|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_7": 8,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_7|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|not_provided": 2,
    "Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|Spastic_paraplegia|Memory_impairment|Seizure|Gait_ataxia|Dysarthria|Spastic_paraparesis|Cerebral_cortical_atrophy": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "Spastic_Paraplegia|_Recessive|Optic_nerve_hypoplasia|Sensorimotor_neuropathy|Spastic_ataxia|SPG7-related_disorder|Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Hereditary_ataxia|Retinal_dystrophy|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|Spastic_paraparesis|Gait_ataxia|Cerebral_cortical_atrophy|Dysarthria|Intellectual_disability": 1,
    "SPG7-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_7|SPG7-related_disorder": 1,
    "SPG7-related_disorder|Hereditary_spastic_paraplegia_7|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_7": 2,
    "not_provided|Hereditary_spastic_paraplegia_7|not_specified": 3,
    "Inborn_genetic_diseases|SPG7-related_disorder|Hereditary_ataxia|not_provided|Mitochondrial_disease|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_7|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "not_specified|Hereditary_spastic_paraplegia_7|Hereditary_spastic_paraplegia": 1,
    "not_specified|Hereditary_spastic_paraplegia_7|Spastic_Paraplegia|_Recessive": 1,
    "Hereditary_spastic_paraplegia_7|not_provided|Spastic_ataxia": 1,
    "not_provided|Hereditary_spastic_paraplegia_7|Hereditary_spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_7|SPG7-related_disorder|not_provided": 1,
    "SPG7-related_disorder|not_specified|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Retinal_dystrophy|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|SPG7-related_disorder|not_specified": 1,
    "Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Leukoencephalopathy_with_vanishing_white_matter_1|not_provided|Hereditary_spastic_paraplegia_7": 1,
    "Intellectual_disability|Spastic_ataxia|Sensorimotor_neuropathy": 1,
    "Hereditary_spastic_paraplegia_7|Hereditary_pancreatitis": 1,
    "SPG7-related_disorder|not_specified|Hereditary_spastic_paraplegia_7": 1,
    "Hereditary_spastic_paraplegia_7|Retinal_dystrophy": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7": 1,
    "SPG7-related_disorder|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_7|Spastic_ataxia": 1,
    "RPL13-related_disorder": 1,
    "Spondyloepimetaphyseal_dysplasia|_Isidor-Toutain_type|not_provided": 2,
    "Spondyloepimetaphyseal_dysplasia|_Isidor-Toutain_type|not_provided|Spondyloepimetaphyseal_dysplasia": 1,
    "Spondyloepimetaphyseal_dysplasia|Spondyloepimetaphyseal_dysplasia|_Isidor-Toutain_type": 1,
    "Spondyloepimetaphyseal_dysplasia|_Isidor-Toutain_type|Spondyloepimetaphyseal_dysplasia": 1,
    "Spondyloepimetaphyseal_dysplasia|_Isidor-Toutain_type": 9,
    "RPL13-related_disorder|Spondyloepimetaphyseal_dysplasia|_Isidor-Toutain_type|not_provided": 1,
    "Inborn_genetic_diseases|CHMP1A-related_disorder": 1,
    "not_specified|not_provided|CHMP1A-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_8": 7,
    "not_provided|CHMP1A-related_disorder": 3,
    "Pontocerebellar_hypoplasia_type_8|Pontocerebellar_hypoplasia_type_1A": 1,
    "CHMP1A-related_disorder|not_provided": 2,
    "not_provided|not_specified|CHMP1A-related_disorder": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_8": 1,
    "CHMP1A-related_disorder|not_provided|not_specified": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_8|Inborn_genetic_diseases": 1,
    "CHMP1A-related_disorder|not_provided|Pontocerebellar_hypoplasia_type_8": 1,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_8": 1,
    "not_specified|Pontocerebellar_hypoplasia_type_8|not_provided|CHMP1A-related_disorder": 1,
    "not_provided|CHMP1A-related_disorder|Inborn_genetic_diseases": 1,
    "Al_Kaissi_syndrome|not_provided": 6,
    "Inborn_genetic_diseases|Al_Kaissi_syndrome": 2,
    "not_provided|Al_Kaissi_syndrome": 5,
    "Al_Kaissi_syndrome": 23,
    "not_provided|Inborn_genetic_diseases|Al_Kaissi_syndrome": 1,
    "CDK10-related_disorder": 9,
    "Inborn_genetic_diseases|Al_Kaissi_syndrome|not_provided": 1,
    "not_provided|CDK10-related_disorder": 1,
    "Al_Kaissi_syndrome|Abnormal_brain_morphology|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases": 15,
    "Fanconi_anemia|FANCA-related_disorder|Inborn_genetic_diseases": 7,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases": 26,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_specified|not_provided": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 9,
    "Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|Fanconi_anemia|FANCA-related_disorder": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 27,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided": 5,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_A": 31,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A": 34,
    "not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided": 2,
    "Fanconi_anemia|Inborn_genetic_diseases|not_specified|Fanconi_anemia_complementation_group_A": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 31,
    "Fanconi_anemia_complementation_group_A|Neuroblastoma|Fanconi_anemia": 1,
    "FANCA-related_disorder": 19,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_specified|not_provided": 6,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|not_provided": 2,
    "FANCA-related_disorder|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 7,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Fanconi_anemia|not_provided": 2,
    "not_specified|FANCA-related_disorder|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_A|Microcephaly|Fanconi_anemia|not_specified|Ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_A|Microcephaly|Fanconi_anemia": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia": 16,
    "Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|Fanconi_anemia": 22,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 1,
    "Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 2,
    "FANCA-related_disorder|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 4,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided": 16,
    "Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|Inborn_genetic_diseases": 2,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder|not_provided|Fanconi_anemia": 2,
    "FANCA-related_disorder|Fanconi_anemia": 12,
    "FANCA-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided": 1,
    "not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 4,
    "Fanconi_anemia_complementation_group_A|not_specified|Fanconi_anemia": 6,
    "not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 27,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified": 4,
    "not_specified|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_A|not_specified|not_provided|Fanconi_anemia|FANCA-related_disorder": 2,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|FANCA-related_disorder|not_specified|not_provided": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified|not_provided": 3,
    "not_specified|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia_complementation_group_A|not_specified|not_provided": 4,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|FANCA-related_disorder": 3,
    "not_specified|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A": 26,
    "not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 5,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 7,
    "not_specified|Ovarian_cancer|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided|Inborn_genetic_diseases": 2,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A": 2,
    "FANCA-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 5,
    "Inborn_genetic_diseases|FANCA-related_disorder|not_specified|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases|FANCA-related_disorder|not_provided": 1,
    "Fanconi_anemia_complementation_group_A|not_specified": 6,
    "not_provided|Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Fanconi_anemia": 3,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided|not_specified": 1,
    "Fanconi_anemia|FANCA-related_disorder": 7,
    "See_cases|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases": 3,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Fanconi_anemia": 5,
    "Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|Fanconi_anemia|not_provided": 2,
    "FANCA-related_disorder|Fanconi_anemia|Inborn_genetic_diseases": 5,
    "Ovarian_cancer|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|Fanconi_anemia": 2,
    "not_provided|Fanconi_anemia|FANCA-related_disorder|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases": 16,
    "Fanconi_anemia|FANCA-related_disorder|not_provided|not_specified": 1,
    "Fanconi_anemia|not_provided|Premature_ovarian_failure|Fanconi_anemia_complementation_group_A": 1,
    "Inborn_genetic_diseases|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Pediatric_high-grade_glioma": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_A|not_provided": 2,
    "FANCA-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 4,
    "Inborn_genetic_diseases|FANCA-related_disorder|Fanconi_anemia": 5,
    "Inborn_genetic_diseases|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|FANCA-related_disorder|not_specified": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 2,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided|not_specified": 3,
    "FANCA-related_disorder|Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_specified": 5,
    "not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases": 3,
    "FANCA-related_disorder|not_specified|not_provided|Hepatoblastoma|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "FANCA-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified|not_provided": 2,
    "not_provided|Fanconi_anemia|Inborn_genetic_diseases|not_specified|Fanconi_anemia_complementation_group_A|FANCA-related_disorder": 1,
    "not_provided|Fanconi_anemia_complementation_group_A|not_specified|Fanconi_anemia": 5,
    "FANCA-related_disorder|not_provided|Fanconi_anemia": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_A": 2,
    "not_provided|FANCA-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified": 1,
    "Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_A": 3,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder": 3,
    "Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|FANCA-related_disorder": 1,
    "FANCA-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified": 1,
    "Fanconi_anemia_complementation_group_A|not_specified|Fanconi_anemia|FANCA-related_disorder": 1,
    "not_specified|not_provided|Fanconi_anemia|Prostate_cancer|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia_complementation_group_A|not_specified|not_provided|Fanconi_anemia": 5,
    "not_provided|FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases": 1,
    "FANCA-related_disorder|Fanconi_anemia|Inborn_genetic_diseases|not_specified|Fanconi_anemia_complementation_group_A": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_specified|not_provided|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_specified": 9,
    "Fanconi_anemia|FANCA-related_disorder|Fanconi_anemia_complementation_group_A": 1,
    "not_specified|Inborn_genetic_diseases|Fanconi_anemia": 3,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_A|not_specified|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "not_specified|Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 2,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided": 3,
    "not_provided|Fanconi_anemia_complementation_group_A|not_specified": 6,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|Ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|FANCA-related_disorder|not_provided": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided|Inborn_genetic_diseases|FANCA-related_disorder": 1,
    "not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases|FANCA-related_disorder": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_provided": 2,
    "not_specified|FANCA-related_disorder|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 5,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Neuroblastoma|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|not_provided|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A": 2,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia": 2,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases": 3,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|See_cases": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|FANCA-related_disorder": 2,
    "not_specified|FANCA-related_disorder|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia|FANCA-related_disorder|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|See_cases|Fanconi_anemia": 1,
    "not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases": 2,
    "Fanconi_anemia|Abnormality_of_blood_and_blood-forming_tissues": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|FANCA-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|FANCA-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 2,
    "Fanconi_anemia|Inborn_genetic_diseases|not_provided|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia|not_provided|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|FANCA-related_disorder|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided|FANCA-related_disorder|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|not_specified|FANCA-related_disorder|Fanconi_anemia_complementation_group_A|not_provided": 1,
    "Fanconi_anemia|not_specified|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_provided|FANCA-related_disorder": 1,
    "not_provided|FANCA-related_disorder": 1,
    "FANCA-related_disorder|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_A": 1,
    "Fanconi_anemia|Ovarian_cancer|Fanconi_anemia_complementation_group_A": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 3,
    "Fanconi_anemia|Inborn_genetic_diseases|FANCA-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|FANCA-related_disorder": 2,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|FANCA-related_disorder|not_specified": 1,
    "Ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_specified": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|FANCA-related_disorder": 3,
    "Inborn_genetic_diseases|Fanconi_anemia|FANCA-related_disorder|Fanconi_anemia_complementation_group_A": 4,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "Inborn_genetic_diseases|FANCA-related_disorder": 2,
    "Fanconi_anemia|FANCA-related_disorder|not_provided|Fanconi_anemia_complementation_group_A": 1,
    "not_specified|Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_provided": 1,
    "Fanconi_anemia_complementation_group_A|not_provided|FANCA-related_disorder|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|FANCA-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "not_specified|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|Fanconi_anemia|FANCA-related_disorder": 2,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided": 2,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Fanconi_anemia|not_specified": 1,
    "not_provided|Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A": 2,
    "not_provided|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_A": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia_complementation_group_A|Pituitary_stalk_interruption_syndrome": 1,
    "Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|not_specified": 3,
    "Fanconi_anemia_complementation_group_A|not_provided|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|not_provided|not_specified": 1,
    "Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|not_specified|Fanconi_anemia": 1,
    "FANCA-related_disorder|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 1,
    "FANCA-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 1,
    "not_specified|Fanconi_anemia_complementation_group_A|not_provided|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia_complementation_group_A|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Fanconi_anemia_complementation_group_A|not_specified|Fanconi_anemia|FANCA-related_disorder": 1,
    "not_provided|Fanconi_anemia|FANCA-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Malignant_tumor_of_breast": 1,
    "FANCA-related_disorder|Fanconi_anemia|not_specified|not_provided": 1,
    "Fanconi_anemia|not_specified|not_provided|Fanconi_anemia_complementation_group_A": 1,
    "not_specified|FANCA-related_disorder|not_provided|Fanconi_anemia_complementation_group_A|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|not_specified|FANCA-related_disorder": 1,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|Ovarian_cancer": 1,
    "FANCA-related_disorder|Fanconi_anemia|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases": 1,
    "not_specified|Fanconi_anemia_complementation_group_A|not_provided|FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCA-related_disorder|Fanconi_anemia_complementation_group_A|Inborn_genetic_diseases|not_provided": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_A|not_provided": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_A|not_provided": 1,
    "Fanconi_anemia|FANCA-related_disorder|not_provided": 2,
    "FANCA-related_disorder|Inborn_genetic_diseases|not_specified|Fanconi_anemia": 1,
    "FANCA-related_disorder|Inborn_genetic_diseases|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_A|Fanconi_anemia|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|not_provided|Fanconi_anemia_complementation_group_A|not_specified": 1,
    "Fanconi_anemia_complementation_group_A|not_specified|Fanconi_anemia|not_provided": 1,
    "Fanconi_anemia_complementation_group_A|FANCA-related_disorder|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "not_provided|Macular_degeneration|_age-related|_neovascular_type": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 288,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 22,
    "Malignant_Melanoma_Susceptibility": 4,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 56,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_specified": 67,
    "MC1R-related_disorder|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "Familial_melanoma|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|bilateral_breast_cancer|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_provided": 8,
    "Tyrosinase-positive_oculocutaneous_albinism|not_specified": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Skin/hair/eye_pigmentation_2|_blond_hair/fair_skin|Malignant_tumor_of_breast|not_provided|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Tyrosinase-positive_oculocutaneous_albinism": 4,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_provided|MC1R-related_disorder|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific": 1,
    "Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism|not_provided|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_specified|not_provided": 4,
    "not_provided|Skin_and_Hair_Hypopigmentation|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Skin/hair/eye_pigmentation_2|_blond_hair/fair_skin|Skin/hair/eye_pigmentation_2|_red_hair/fair_skin|not_provided|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2": 2,
    "Tyrosinase-positive_oculocutaneous_albinism|MC1R-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "MC1R-related_disorder": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|MC1R-related_disorder": 1,
    "not_provided|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 4,
    "UV-induced_skin_damage|_susceptibility_to": 2,
    "not_specified|not_provided|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|ALBINISM|_OCULOCUTANEOUS|_TYPE_II|_MODIFIER_OF|Skin/hair/eye_pigmentation_2|_red_hair/fair_skin": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|not_provided": 1,
    "Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism|not_specified|not_provided": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Tyrosinase-positive_oculocutaneous_albinism|not_specified": 1,
    "UV-induced_skin_damage|_susceptibility_to|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_specified|not_provided|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|ALBINISM|_OCULOCUTANEOUS|_TYPE_II|_MODIFIER_OF|Skin/hair/eye_pigmentation_2|_red_hair/fair_skin|Malignant_tumor_of_breast": 1,
    "Familial_melanoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_specified|MC1R-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|not_specified|not_provided": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Skin_and_Hair_Hypopigmentation|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Skin_and_Hair_Hypopigmentation|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Malignant_Melanoma_Susceptibility": 1,
    "Skin_and_Hair_Hypopigmentation|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Tyrosinase-positive_oculocutaneous_albinism|Hereditary_cancer-predisposing_syndrome": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_provided|not_specified": 2,
    "SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2": 3,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_provided|MC1R-related_disorder": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "MC1R-related_disorder|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_specified": 5,
    "Malignant_Melanoma_Susceptibility|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|not_provided|Tyrosinase-positive_oculocutaneous_albinism|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2": 1,
    "Tyrosinase-positive_oculocutaneous_albinism|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|not_specified": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_5|SKIN/HAIR/EYE_PIGMENTATION|_VARIATION_IN|_2|Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Increased_analgesia_from_kappa-opioid_receptor_agonist|_female-specific|Melanoma|_cutaneous_malignant|_susceptibility_to|_5": 1,
    "not_provided|Skin_and_Hair_Hypopigmentation|Skin/hair/eye_pigmentation_2|_red_hair/fair_skin|Melanoma|_cutaneous_malignant|_susceptibility_to|_5|Melanoma|MC1R-related_disorder|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "Skin_and_Hair_Hypopigmentation|Tyrosinase-positive_oculocutaneous_albinism": 1,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1": 6,
    "Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|Developmental_disorder|not_provided": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|Complex_cortical_dysplasia_with_other_brain_malformations_1": 2,
    "TUBB3-related_disorder|Complex_cortical_dysplasia_with_other_brain_malformations_1|not_provided": 1,
    "not_specified|TUBB3-related_disorder|not_provided": 2,
    "not_provided|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement": 3,
    "TUBB3-related_tubulinopathy|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|TUBB3-related_disorder": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement": 5,
    "Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|not_provided|TUBB3-related_disorder|Intellectual_disability": 1,
    "TUBB3-related_disorder": 8,
    "not_provided|TUBB3-related_disorder": 4,
    "TUBB3-related_tubulinopathy": 1,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1|Brain_malformation|Congenital_fibrosis_of_extraocular_muscles": 1,
    "TUBB3-related_disorder|not_specified|not_provided": 1,
    "TUBB3-related_disorder|not_provided|not_specified": 1,
    "TUBB3-related_disorder|not_provided": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|Congenital_Fibrosis_of_the_Extraocular_Muscles_1B|Congenital_fibrosis_of_extraocular_muscles_type_1": 1,
    "Inborn_genetic_diseases|Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|Inborn_genetic_diseases|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1": 1,
    "not_provided|TUBB3-related_disorder|not_specified": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_1|not_provided": 5,
    "not_provided|not_specified|TUBB3-related_disorder": 1,
    "Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|Complex_cortical_dysplasia_with_other_brain_malformations_1|not_provided": 1,
    "TUBB3-related_tubulinopathy|not_provided": 1,
    "not_provided|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|TUBB3-related_disorder|Complex_cortical_dysplasia_with_other_brain_malformations_1": 1,
    "TUBB3-related_tubulinopathy|not_provided|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|TUBB3-related_disorder": 1,
    "Abnormal_cerebral_morphology|TUBB3-related_tubulinopathy|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1": 1,
    "not_specified|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1|TUBB3-related_disorder": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_8|Complex_cortical_dysplasia_with_other_brain_malformations_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|TUBB3-related_disorder": 1,
    "TUBB3-Releated_Disorders|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement|TUBB3-related_disorder": 1,
    "TUBB3-related_tubulinopathy|not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_1|Fibrosis_of_extraocular_muscles|_congenital|_3A|_with_or_without_extraocular_involvement": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_1|TUBB3-related_disorder": 1,
    "Primary_ciliary_dyskinesia_33|not_provided": 12,
    "Primary_ciliary_dyskinesia_33": 241,
    "Primary_ciliary_dyskinesia_33|GAS8-related_disorder": 8,
    "See_cases|Primary_ciliary_dyskinesia_33|Inborn_genetic_diseases": 1,
    "not_provided|Primary_ciliary_dyskinesia_33": 7,
    "GAS8-related_disorder|Primary_ciliary_dyskinesia_33": 3,
    "not_provided|GAS8-related_disorder": 1,
    "Primary_ciliary_dyskinesia_33|Inborn_genetic_diseases": 11,
    "Primary_ciliary_dyskinesia_33|not_provided|GAS8-related_disorder": 1,
    "GAS8-related_disorder": 3,
    "Primary_ciliary_dyskinesia_33|Primary_ciliary_dyskinesia": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_33": 9,
    "not_specified|Primary_ciliary_dyskinesia_33|not_provided": 3,
    "not_provided|Primary_ciliary_dyskinesia_33|Inborn_genetic_diseases": 1,
    "Primary_ciliary_dyskinesia_33|GAS8-related_disorder|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia_33|not_specified": 1,
    "not_provided|GAS8-related_disorder|Primary_ciliary_dyskinesia_33": 1,
    "Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia_33": 1,
    "GAS8-related_disorder|not_provided|Primary_ciliary_dyskinesia_33": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_33|not_provided": 1,
    "Primary_ciliary_dyskinesia_33|not_specified|not_provided": 1,
    "VPS53-related_disorder": 6,
    "VPS53-related_disorder|not_provided": 4,
    "Pontocerebellar_hypoplasia_type_2E": 18,
    "not_specified|Pontocerebellar_hypoplasia_type_2E|not_provided": 1,
    "not_provided|VPS53-related_disorder": 3,
    "not_provided|not_specified|VPS53-related_disorder": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_2E": 7,
    "Pontocerebellar_hypoplasia_type_2E|not_provided|not_specified|Microcephaly": 1,
    "not_provided|VPS53-related_disorder|not_specified": 1,
    "Pontocerebellar_hypoplasia_type_2E|not_provided": 5,
    "not_specified|Pontocerebellar_hypoplasia_type_2E": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_2E|Pontoneocerebellar_hypoplasia": 1,
    "Pontocerebellar_hypoplasia_type_2E|not_provided|not_specified": 1,
    "Pontoneocerebellar_hypoplasia|not_provided|Pontocerebellar_hypoplasia_type_2E": 1,
    "Neurodevelopmental_abnormality|Pontocerebellar_hypoplasia_type_2E|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_2E": 3,
    "not_specified|not_provided|VPS53-related_disorder": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_2E": 1,
    "Pontocerebellar_hypoplasia_type_2E|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|GEMIN4-related_disorder": 7,
    "GEMIN4-related_disorder": 14,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities": 3,
    "Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities": 11,
    "Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities|not_provided": 4,
    "Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities|Microcephaly|Severe_dystonia|Developmental_cataract|Global_developmental_delay": 1,
    "GEMIN4-related_disorder|not_provided": 6,
    "GEMIN4-related_disorder|Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities|not_provided": 2,
    "not_provided|GEMIN4-related_disorder|not_specified": 1,
    "not_specified|GEMIN4-related_disorder": 3,
    "Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities|not_specified": 1,
    "not_specified|not_provided|GEMIN4-related_disorder": 1,
    "not_specified|Neurodevelopmental_disorder_with_microcephaly|_cataracts|_and_renal_abnormalities": 1,
    "NXN-related_disorder": 2,
    "Robinow_syndrome|_autosomal_recessive_2": 3,
    "not_provided|NXN-related_disorder": 9,
    "NXN-related_disorder|not_provided": 4,
    "Robinow_syndrome|_autosomal_recessive_2|not_provided": 1,
    "Robinow_syndrome|_autosomal_recessive_2|not_provided|Distal_shortening_of_limbs": 1,
    "Robinow_syndrome|_autosomal_recessive_2|NXN-related_disorder|not_provided": 1,
    "TIMM22-related_disorder": 1,
    "TIMM22-related_disorder|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_43": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_43": 2,
    "ABR-related_disorder": 5,
    "not_provided|BHLHA9-related_disorder": 1,
    "Mesoaxial_synostotic_syndactyly_with_phalangeal_reduction": 4,
    "Camptosynpolydactyly|_complex": 1,
    "BHLHA9-related_disorder|Camptosynpolydactyly|_complex|Mesoaxial_synostotic_syndactyly_with_phalangeal_reduction|not_provided": 1,
    "BHLHA9-related_disorder": 1,
    "Mesoaxial_synostotic_syndactyly_with_phalangeal_reduction|not_provided|BHLHA9-related_disorder": 1,
    "not_provided|YWHAE-related_disorder": 1,
    "YWHAE-related_disorder|not_provided": 5,
    "YWHAE-related_disorder": 2,
    "YWHAE-associated_disorder": 1,
    "MYO1C-related_disorder": 11,
    "MYO1C-related_disorder|not_provided": 3,
    "not_provided|MYO1C-related_disorder": 3,
    "MYO1C-related_disorder|not_provided|not_specified": 1,
    "MYO1C-related_disorder|not_specified": 1,
    "not_provided|MYO1C-related_disorder|not_specified": 1,
    "Miller_Dieker_syndrome": 1,
    "Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability": 18,
    "not_provided|INPP5K-related_disorder": 3,
    "INPP5K-related_disorder|not_provided": 3,
    "INPP5K-related_disorder": 3,
    "Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability": 1,
    "not_provided|Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability": 2,
    "Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability|not_provided|INPP5K-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability|not_provided": 2,
    "Precursor_Cell_Lymphoblastic_Leukemia-Lymphoma|Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability": 1,
    "Congenital_myopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_intellectual_disability)|_type_B1|Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability|Congenital_muscular_dystrophy|not_provided": 1,
    "INPP5K-related_disorder|not_provided|Congenital_muscular_dystrophy_with_cataracts_and_intellectual_disability": 1,
    "Retinitis_pigmentosa_13": 21,
    "Retinal_dystrophy|Retinitis_pigmentosa_13": 1,
    "not_provided|Retinitis_pigmentosa_13": 10,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_13|not_provided": 7,
    "not_provided|Retinitis_pigmentosa_13|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_13|Autosomal_dominant_retinitis_pigmentosa|not_provided|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_13|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_13|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_13|not_provided": 7,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_13": 1,
    "not_provided|PRPF8-related_disorder|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_13|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_13|PRPF8-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_13|Retinal_dystrophy": 1,
    "not_provided|PRPF8-related_disorder": 5,
    "Retinitis_pigmentosa_13|not_provided|Retinal_dystrophy": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_13": 1,
    "Retinitis_pigmentosa_13|Neurodevelopmental_disorder": 1,
    "PRPF8-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_13|not_provided|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_13|not_provided": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_13": 2,
    "Retinitis_pigmentosa_13|not_provided|Retinitis_pigmentosa": 3,
    "not_provided|Retinitis_pigmentosa|PRPF8-related_disorder": 1,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|PRPF8-related_disorder": 1,
    "PRPF8-related_disorder|not_provided": 2,
    "Retinitis_Pigmentosa|_Dominant|not_provided": 5,
    "Retinal_dystrophy|not_provided|Retinitis_Pigmentosa|_Dominant": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_13|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_13": 1,
    "Retinal_dystrophy|not_provided|PRPF8-related_disorder": 1,
    "Choroideremia|not_provided": 31,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 18,
    "Hydrocephalus|_congenital|_3|_with_brain_anomalies": 3,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 2,
    "WDR81-related_disorder": 13,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies": 4,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Severe_brain_malformation|Severe_cerebellar_hypoplasia|Neonatal_death|Hydranencephaly|not_provided|Hydrocephalus|_congenital|_3|_with_brain_anomalies": 1,
    "not_provided|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 5,
    "not_provided|Inborn_genetic_diseases|WDR81-related_disorder": 1,
    "Inborn_genetic_diseases|WDR81-related_disorder": 1,
    "not_provided|WDR81-related_disorder": 6,
    "WDR81-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "WDR81-related_disorder|not_provided": 8,
    "Inborn_genetic_diseases|Exstrophy-epispadias_complex": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_provided": 2,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies": 2,
    "Intellectual_disability|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Inborn_genetic_diseases": 1,
    "Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_provided": 2,
    "Hydrocephalus|_congenital|_3|_with_brain_anomalies|not_specified|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 2,
    "Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 4,
    "WDR81-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_specified": 1,
    "Hydrocephalus|_congenital|_3|_with_brain_anomalies|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 2,
    "Inborn_genetic_diseases|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_provided": 1,
    "Microcephaly|Epileptic_encephalopathy": 1,
    "WDR81-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|WDR81-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "Inborn_genetic_diseases|Cerebellar_ataxia|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_provided": 1,
    "not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Inborn_genetic_diseases": 2,
    "not_provided|Intellectual_disability|WDR81-related_disorder": 1,
    "Microlissencephaly": 1,
    "not_specified|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_provided": 2,
    "Inborn_genetic_diseases|Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "not_specified|Hydrocephalus|_congenital|_3|_with_brain_anomalies|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|WDR81-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|WDR81-related_disorder": 2,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "WDR81-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "Hydrocephalus|_congenital|_3|_with_brain_anomalies|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2": 1,
    "not_provided|WDR81-related_disorder|Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies": 1,
    "Cerebellar_ataxia|_intellectual_disability|_and_dysequilibrium_syndrome_2|Hydrocephalus|_congenital|_3|_with_brain_anomalies|not_provided": 1,
    "not_provided|SERPINF2-related_disorder": 3,
    "SERPINF2-related_disorder": 4,
    "SERPINF2-related_disorder|not_provided": 2,
    "Alpha-2-plasmin_inhibitor_deficiency|not_specified": 1,
    "Alpha-2-plasmin_inhibitor_deficiency": 3,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_Imperfecta|_Recessive": 1,
    "Osteogenesis_imperfecta_type_6": 42,
    "not_provided|Osteogenesis_imperfecta_type_6|Osteogenesis_imperfecta": 1,
    "not_provided|Osteogenesis_imperfecta_type_6": 14,
    "not_provided|SERPINF1-related_disorder": 3,
    "Osteogenesis_imperfecta_type_6|not_provided": 10,
    "not_provided|Osteogenesis_imperfecta|not_specified|Osteogenesis_imperfecta_type_6": 1,
    "Osteogenesis_imperfecta_type_6|SERPINF1-related_disorder|Osteogenesis_imperfecta|not_provided": 1,
    "not_specified|Osteogenesis_imperfecta_type_6|Osteogenesis_imperfecta|not_provided": 1,
    "Osteoporosis|SERPINF1-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_6": 1,
    "not_provided|SERPINF1-related_disorder|not_specified": 1,
    "Osteogenesis_imperfecta_type_6|not_provided|Osteogenesis_imperfecta": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_6": 3,
    "not_specified|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_6": 1,
    "SERPINF1-related_disorder|Osteogenesis_imperfecta|not_provided": 1,
    "SERPINF1-related_disorder": 5,
    "Osteogenesis_imperfecta_type_6|not_provided|not_specified": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_6": 3,
    "SERPINF1-related_disorder|not_provided|Osteogenesis_imperfecta": 1,
    "SERPINF1-related_disorder|not_provided": 2,
    "not_provided|Osteogenesis_imperfecta_type_6|Osteogenesis_imperfecta|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "not_provided|Osteogenesis_imperfecta_type_6|SERPINF1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Osteogenesis_imperfecta_type_6": 3,
    "Osteogenesis_imperfecta_type_6|Osteogenesis_imperfecta": 1,
    "not_specified|Osteogenesis_imperfecta|Inborn_genetic_diseases": 1,
    "not_specified|Osteogenesis_imperfecta_type_6|not_provided": 1,
    "not_provided|not_specified|SERPINF1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Osteogenesis_imperfecta_type_6": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_6": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_6|RPA1-related_short_telomere_syndrome": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_telomere-related|_6|not_specified": 1,
    "RPA1-related_disorder": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1": 12,
    "not_provided|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair": 6,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1|Inborn_genetic_diseases": 2,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair|Inborn_genetic_diseases": 1,
    "DPH1-related_disorder": 4,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1|not_provided": 2,
    "Inborn_genetic_diseases|DPH1-related_disorder|not_provided|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair|not_provided": 2,
    "not_provided|DPH1-related_disorder": 3,
    "DPH1-related_disorder|not_provided": 2,
    "DPH1-related_disorder|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair|Global_developmental_delay|Cerebellar_vermis_hypoplasia|Dandy-Walker_syndrome|Hydrocephalus": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair": 1,
    "not_specified|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1": 1,
    "not_provided|Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair": 1,
    "Developmental_delay_with_short_stature|_dysmorphic_facial_features|_and_sparse_hair_1|not_specified": 1,
    "Corpus_callosum_agenesis-abnormal_genitalia_syndrome": 6,
    "TSR1-related_disorder": 3,
    "not_provided|Primary_microcephaly|not_specified": 1,
    "Lissencephaly/Subcortical_Band_Heterotopia": 10,
    "Lissencephaly_due_to_LIS1_mutation": 101,
    "Intellectual_disability|not_provided|Subcortical_band_heterotopia|Lissencephaly_due_to_LIS1_mutation|Lissencephaly": 1,
    "PAFAH1B1-related_disorder|not_provided": 3,
    "not_provided|Lissencephaly_due_to_LIS1_mutation": 23,
    "Lissencephaly_due_to_LIS1_mutation|not_provided": 10,
    "Intellectual_disability|Lissencephaly_due_to_LIS1_mutation|not_provided|not_specified": 1,
    "Lissencephaly_due_to_LIS1_mutation|not_provided|Inborn_genetic_diseases": 1,
    "PAFAH1B1-related_disorder": 3,
    "not_provided|Abnormal_cerebral_morphology": 1,
    "Abnormal_cortical_gyration": 8,
    "not_provided|PAFAH1B1-related_disorder": 2,
    "Subcortical_band_heterotopia": 2,
    "Lissencephaly_due_to_LIS1_mutation|not_specified|not_provided": 1,
    "Lissencephaly|Lissencephaly_due_to_LIS1_mutation|Inborn_genetic_diseases|not_provided": 1,
    "PAFAH1B1-Associated_Lissencephaly/Subcortical_Band_Heterotopia": 1,
    "PAFAH1B1-related_disorder|not_provided|Inborn_genetic_diseases|Lissencephaly_due_to_LIS1_mutation": 1,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_due_to_LIS1_mutation": 1,
    "Subcortical_band_heterotopia|not_provided": 1,
    "PAFAH1B1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Lissencephaly_due_to_LIS1_mutation|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Classic_lissencephaly": 1,
    "Lissencephaly_due_to_LIS1_mutation|Neurodevelopmental_delay|Lissencephaly": 1,
    "not_provided|not_specified|Lissencephaly_due_to_LIS1_mutation": 1,
    "Lissencephaly/Subcortical_Band_Heterotopia|not_provided": 2,
    "Premature_ovarian_failure_25": 2,
    "Premature_ovarian_failure_25|Spermatogenic_failure_96": 1,
    "Spongy_degeneration_of_central_nervous_system": 348,
    "Spongy_degeneration_of_central_nervous_system|Inborn_genetic_diseases": 17,
    "Canavan_Disease|_Familial_Form|Spongy_degeneration_of_central_nervous_system": 10,
    "ASPA-related_disorder|Spongy_degeneration_of_central_nervous_system": 2,
    "Spongy_degeneration_of_central_nervous_system|not_specified": 3,
    "Inborn_genetic_diseases|Spongy_degeneration_of_central_nervous_system": 7,
    "Canavan_Disease|_Familial_Form|not_provided|Spongy_degeneration_of_central_nervous_system": 5,
    "not_specified|Spongy_degeneration_of_central_nervous_system": 5,
    "Spongy_degeneration_of_central_nervous_system|not_provided": 4,
    "not_provided|Spongy_degeneration_of_central_nervous_system": 2,
    "Canavan_Disease|_Familial_Form": 5,
    "Canavan_Disease|_Familial_Form|Inborn_genetic_diseases|not_provided|Spongy_degeneration_of_central_nervous_system|Mild_Canavan_disease": 1,
    "not_provided|Canavan_Disease|_Familial_Form|Inborn_genetic_diseases|Spongy_degeneration_of_central_nervous_system": 1,
    "Inborn_genetic_diseases|Spongy_degeneration_of_central_nervous_system|not_provided": 1,
    "Spongy_degeneration_of_central_nervous_system|Canavan_Disease|_Familial_Form": 6,
    "Spongy_degeneration_of_central_nervous_system|Canavan_Disease|_Familial_Form|not_provided": 1,
    "Canavan_Disease|_Familial_Form|Inborn_genetic_diseases|not_provided|Spongy_degeneration_of_central_nervous_system": 3,
    "Abnormality_of_metabolism/homeostasis|Spongy_degeneration_of_central_nervous_system": 1,
    "Inborn_genetic_diseases|not_provided|Spongy_degeneration_of_central_nervous_system": 1,
    "not_provided|Intellectual_disability|Canavan_Disease|_Familial_Form|Spongy_degeneration_of_central_nervous_system": 1,
    "Mild_Canavan_disease|Spongy_degeneration_of_central_nervous_system": 1,
    "Canavan_Disease|_Familial_Form|Spongy_degeneration_of_central_nervous_system|not_provided|Autism": 1,
    "not_specified|Spongy_degeneration_of_central_nervous_system|not_provided": 1,
    "Spongy_degeneration_of_central_nervous_system|ASPA-related_disorder|Inborn_genetic_diseases": 1,
    "ASPA-related_disorder|Canavan_Disease|_Familial_Form|Inborn_genetic_diseases|not_provided|Spongy_degeneration_of_central_nervous_system": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Spongy_degeneration_of_central_nervous_system": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Spongy_degeneration_of_central_nervous_system": 1,
    "Spongy_degeneration_of_central_nervous_system|not_provided|not_specified": 1,
    "ASPA-related_disorder": 1,
    "not_provided|Spongy_degeneration_of_central_nervous_system|not_specified": 1,
    "Spongy_degeneration_of_central_nervous_system|Inborn_genetic_diseases|Fraser_syndrome_3": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Spongy_degeneration_of_central_nervous_system": 1,
    "Spongy_degeneration_of_central_nervous_system|ASPA-related_disorder": 2,
    "not_provided|Canavan_Disease|_Familial_Form|Spongy_degeneration_of_central_nervous_system": 1,
    "not_provided|Spongy_degeneration_of_central_nervous_system|Inborn_genetic_diseases": 1,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma": 111,
    "Olmsted_syndrome_1": 16,
    "not_provided|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma": 24,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided": 32,
    "not_provided|Olmsted_syndrome_1": 3,
    "TRPV3-related_disorder|not_provided|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma": 1,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided|Olmsted_syndrome_1": 6,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_specified|not_provided": 2,
    "not_provided|TRPV3-related_disorder": 3,
    "Inborn_genetic_diseases|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma": 3,
    "Olmsted_syndrome_1|not_provided": 2,
    "Inborn_genetic_diseases|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|Olmsted_syndrome_1": 2,
    "not_provided|Olmsted_syndrome_1|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma": 2,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|Olmsted_syndrome_1": 3,
    "TRPV3-related_disorder|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided": 4,
    "TRPV3-related_disorder": 3,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|Inborn_genetic_diseases": 2,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|TRPV3-related_disorder|not_provided": 2,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|Olmsted_syndrome_1|not_provided": 3,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided|TRPV3-related_disorder": 1,
    "Inborn_genetic_diseases|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided": 1,
    "TRPV3-related_disorder|not_provided": 1,
    "Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided|Inborn_genetic_diseases": 1,
    "TRPV3-related_disorder|Isolated_focal_non-epidermolytic_palmoplantar_keratoderma|not_provided|Olmsted_syndrome_1": 1,
    "not_provided|SHPK-related_disorder": 2,
    "SHPK-related_disorder|not_provided": 1,
    "not_provided|Isolated_sedoheptulokinase_deficiency": 2,
    "Isolated_sedoheptulokinase_deficiency": 1,
    "Cystinosis": 39,
    "Ocular_cystinosis": 5,
    "Nephropathic_cystinosis|Cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis|not_provided": 1,
    "not_provided|Cystinosis": 1,
    "Nephropathic_cystinosis|Ocular_cystinosis": 24,
    "Ocular_cystinosis|Nephropathic_cystinosis|not_provided": 6,
    "Ocular_cystinosis|Nephropathic_cystinosis": 63,
    "Nephropathic_cystinosis|not_provided|Ocular_cystinosis": 4,
    "Nephropathic_cystinosis|Ocular_cystinosis|not_provided": 2,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis": 20,
    "Cystinosis|Nephropathic_cystinosis": 12,
    "Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 130,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis": 206,
    "Nephropathic_cystinosis|Ocular_cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis": 2,
    "CTNS-related_disorder|Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Cystinosis|Infantile_nephropathic_cystinosis|not_provided": 1,
    "Inborn_genetic_diseases|Ocular_cystinosis|Nephropathic_cystinosis|Juvenile_nephropathic_cystinosis": 4,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis": 12,
    "Ocular_cystinosis|Nephropathic_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Cystinosis|Nephropathic_cystinosis": 1,
    "Nephropathic_cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 1,
    "Nephropathic_cystinosis|Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Inborn_genetic_diseases": 5,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases": 11,
    "Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases": 7,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 16,
    "Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Nephropathic_cystinosis": 2,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 10,
    "not_provided|Nephropathic_cystinosis|Cystinosis|Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis": 1,
    "not_specified|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis|not_provided|Nephropathic_cystinosis": 1,
    "CTNS-related_disorder|not_specified|Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis|not_provided": 1,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|not_provided": 3,
    "Cystinosis|CTNS-related_disorder|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis|not_specified|not_provided|Cystinosis|_atypical_nephropathic": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Cystinosis|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis": 13,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Cystinosis": 2,
    "Inborn_genetic_diseases|not_specified|Ocular_cystinosis|Juvenile_nephropathic_cystinosis": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis": 7,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis|Cystinosis|CTNS-related_disorder": 1,
    "CTNS-related_disorder|Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_provided": 1,
    "Ocular_cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis": 2,
    "Cystinosis|Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis": 4,
    "Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis|not_provided": 3,
    "Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Nephropathic_cystinosis": 3,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis": 3,
    "not_specified|Nephropathic_cystinosis|CTNS-related_disorder|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis": 8,
    "Cystinosis|Ocular_cystinosis|Nephropathic_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Ocular_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis": 1,
    "Cystinosis|_atypical_nephropathic": 1,
    "Ocular_cystinosis|not_provided|Nephropathic_cystinosis": 2,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_provided": 3,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_specified|Nephropathic_cystinosis": 1,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|not_provided|Nephropathic_cystinosis|Cystinosis": 1,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis": 1,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Cystinosis|Inborn_genetic_diseases|CTNS-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|not_specified": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis|Cystinosis|not_provided|Cystinosis|_atypical_nephropathic": 1,
    "not_provided|Cystinosis|Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_provided|Nephropathic_cystinosis": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|CTNS-related_disorder|Inborn_genetic_diseases|Cystinosis": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_specified": 2,
    "Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Ocular_cystinosis": 1,
    "Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Cystinosis|CTNS-related_disorder|not_specified|not_provided|Nephropathic_cystinosis": 1,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_specified|not_provided|Nephropathic_cystinosis": 4,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|CTNS-related_disorder|Cystinosis|Inborn_genetic_diseases|not_provided": 1,
    "Cystinosis|not_specified|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|not_provided": 1,
    "Nephropathic_cystinosis|Cystinosis": 3,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|CTNS-related_disorder|Inborn_genetic_diseases|not_provided|Infantile_nephropathic_cystinosis": 1,
    "Ocular_cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis": 1,
    "Cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 1,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Cystinosis|not_provided": 1,
    "CTNS-related_disorder|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis|not_provided": 1,
    "Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases": 3,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis|Cystinosis": 2,
    "Cystinosis|Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_provided": 1,
    "See_cases|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 1,
    "Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Cystinosis": 2,
    "not_provided|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases": 2,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis": 2,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases|not_provided": 1,
    "Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|CTNS-related_disorder|not_provided": 1,
    "Nephropathic_cystinosis|Inborn_genetic_diseases|Ocular_cystinosis|Juvenile_nephropathic_cystinosis": 3,
    "Ocular_cystinosis|Nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis|Juvenile_nephropathic_cystinosis": 1,
    "CTNS-related_disorder|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Nephropathic_cystinosis": 1,
    "Cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 3,
    "Cystinosis|Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Nephrotic_syndrome|Nephropathic_cystinosis": 1,
    "Nephropathic_cystinosis|Cystinosis|Inborn_genetic_diseases|Juvenile_nephropathic_cystinosis|Ocular_cystinosis": 1,
    "Cystinosis|Nephropathic_cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Nephropathic_cystinosis|not_specified|not_provided": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Nephropathic_cystinosis|not_provided|Inborn_genetic_diseases|Cystinosis": 1,
    "Nephropathic_cystinosis|not_provided": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|Cystinosis|not_provided": 1,
    "Nephropathic_cystinosis|Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_provided": 1,
    "Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Inborn_genetic_diseases|not_specified|not_provided|Nephropathic_cystinosis": 1,
    "Nephropathic_cystinosis|Cystinosis|Ocular_cystinosis|Juvenile_nephropathic_cystinosis|Infantile_nephropathic_cystinosis|Inborn_genetic_diseases": 1,
    "Nephropathic_cystinosis|CTNS-related_disorder|Cystinosis|Juvenile_nephropathic_cystinosis|Ocular_cystinosis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Ocular_cystinosis|Nephropathic_cystinosis": 18,
    "CTNS-related_disorder": 2,
    "not_specified|not_provided|Nephropathic_cystinosis|Ocular_cystinosis": 1,
    "not_provided|Nephropathic_cystinosis|Ocular_cystinosis": 1,
    "Primary_familial_dilated_cardiomyopathy|TAX1BP3-related_arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "P2RX5-related_disorder|not_provided": 1,
    "P2RX5-related_disorder": 1,
    "P2RX1-related_disorder": 15,
    "P2RX1-related_disorder|not_provided": 1,
    "not_specified|P2RX1-related_disorder": 1,
    "ATP2A3-related_disorder": 42,
    "not_provided|ATP2A3-related_disorder": 5,
    "not_specified|ATP2A3-related_disorder|not_provided": 1,
    "not_specified|not_provided|ATP2A3-related_disorder": 1,
    "ATP2A3-related_disorder|not_provided": 2,
    "ANKFY1-related_disorder": 29,
    "not_specified|ANKFY1-related_disorder": 2,
    "ANKFY1-related_disorder|not_provided": 2,
    "ANKFY1-related_disorder|not_specified": 1,
    "SPNS2-related_disorder": 20,
    "not_provided|Hearing_loss|_autosomal_recessive_115": 3,
    "Hearing_loss|_autosomal_recessive_115|not_provided": 4,
    "Hearing_loss|_autosomal_recessive_115|Inborn_genetic_diseases": 2,
    "SPNS2-related_disorder|not_provided": 3,
    "not_provided|SPNS2-related_disorder": 1,
    "SPNS2-related_disorder|not_specified": 1,
    "MYBBP1A-related_condition": 1,
    "not_provided|Asthma|_nasal_polyps|_and_aspirin_intolerance": 1,
    "Neurodegeneration_with_developmental_delay|_early_respiratory_failure|_myoclonic_seizures|_and_brain_abnormalities": 2,
    "Spermatogenic_failure_14": 7,
    "ZMYND15-related_disorder": 4,
    "not_provided|ZMYND15-related_disorder": 1,
    "Spermatogenic_failure_14|Male_infertility": 1,
    "Congenital_myasthenic_syndrome|not_provided": 3,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive": 4,
    "not_provided|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 2,
    "Congenital_myasthenic_syndrome_4C|not_provided|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4A": 842,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_4A": 2,
    "not_provided|Congenital_myasthenic_syndrome|not_specified": 2,
    "Congenital_myasthenic_syndrome|not_specified|not_provided": 2,
    "not_specified|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 33,
    "not_specified|Congenital_myasthenic_syndrome_4A": 4,
    "Congenital_myasthenic_syndrome_4A|not_provided": 28,
    "Congenital_myasthenic_syndrome_4A|not_provided|Congenital_myasthenic_syndrome": 3,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A": 43,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C": 14,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A|CHRNE-related_disorder|not_provided": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4A|CHRNE-related_disorder|Congenital_myasthenic_syndrome": 1,
    "CHRNE-related_disorder|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases": 2,
    "Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A": 8,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|not_specified|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_4A": 15,
    "Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases": 11,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A": 2,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A": 5,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|not_provided": 2,
    "CHRNE-related_disorder|Congenital_myasthenic_syndrome_4A": 4,
    "Congenital_myasthenic_syndrome_4A|not_specified": 3,
    "not_provided|CHRNE-related_disorder": 1,
    "not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome": 5,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 12,
    "not_specified|Congenital_myasthenic_syndrome_4A|not_provided|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4A|not_provided|CHRNE-related_disorder": 2,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|not_specified|not_provided|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|not_provided": 4,
    "not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 3,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4A": 8,
    "not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A": 5,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4B": 6,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|not_provided": 4,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome": 1,
    "not_provided|Congenital_myasthenic_syndrome_4C|not_specified|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome_4A|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B": 3,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A": 1,
    "not_provided|Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases|Congenital_myasthenic_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|not_provided": 1,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_4A": 3,
    "Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 3,
    "not_provided|Congenital_myasthenic_syndrome|CHRNE-related_disorder|Congenital_myasthenic_syndrome_4A": 1,
    "CHRNE-related_disorder|Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A|Abnormality_of_the_musculature": 1,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B": 4,
    "not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome": 2,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|not_provided|CHRNE-related_disorder": 1,
    "not_specified|Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases": 1,
    "CHRNE-related_disorder|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Inborn_genetic_diseases|not_provided|CHRNE-related_disorder|Congenital_myasthenic_syndrome": 1,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Congenital_myasthenic_syndrome_4A": 2,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C": 3,
    "CHRNE-related_disorder|not_specified|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases|not_provided": 3,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4B|Abnormality_of_the_musculature|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome|not_specified|not_provided|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome|not_specified|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4A|not_provided|not_specified|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|not_provided": 2,
    "Congenital_myasthenic_syndrome_4A|not_provided|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome|CHRNE-related_disorder|not_provided|Tip-toe_gait|not_specified|Congenital_myasthenic_syndrome_4A": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome": 1,
    "Neurodevelopmental_delay|Multifocal_seizures": 1,
    "Congenital_myasthenic_syndrome_4A|CHRNE-related_disorder": 4,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|not_provided": 1,
    "CHRNE-related_disorder|Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C|not_provided": 1,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases|Congenital_myasthenic_syndrome": 1,
    "Distal_myopathy|Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_4A": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 1,
    "CHRNE-related_disorder": 1,
    "Congenital_myasthenic_syndrome_4A|not_provided|Congenital_myasthenic_syndrome|CHRNE-related_disorder": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome|not_specified|not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome|not_provided|Inborn_genetic_diseases|CHRNE-related_disorder|Congenital_myasthenic_syndrome_4A": 1,
    "not_specified|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|not_provided": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_4A|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B": 1,
    "not_provided|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|CHRNE-related_disorder|not_provided|Tip-toe_gait": 1,
    "not_provided|Congenital_myasthenic_syndrome|not_specified|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome|not_provided|Abnormality_of_the_musculature|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|CHRNE-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome|not_provided|Myasthenic_syndrome|_congenital|_1B|_fast-channel|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Long_QT_syndrome_2": 1,
    "not_specified|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C": 2,
    "C17orf107-related_condition|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_4A|Abnormality_of_the_musculature|not_provided": 1,
    "not_specified|Congenital_myasthenic_syndrome_4A|not_provided": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4C|not_provided|Abnormality_of_the_musculature|Congenital_myasthenic_syndrome|Slow-Channel_Congenital_Myasthenia_Syndrome": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome|not_provided": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome|not_specified|not_provided|Tip-toe_gait": 1,
    "not_specified|Congenital_myasthenic_syndrome|not_provided|Congenital_myasthenic_syndrome_4A": 2,
    "Congenital_myasthenic_syndrome|CHRNE-related_disorder|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome|Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B|not_provided|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome|not_provided|not_specified|Congenital_myasthenic_syndrome_4A": 1,
    "Congenital_myasthenic_syndrome_4B|Congenital_myasthenic_syndrome|not_specified|not_provided|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C": 1,
    "CHRNE-related_disorder|Congenital_myasthenic_syndrome|not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4A": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_myasthenic_syndrome": 1,
    "not_specified|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome": 1,
    "not_provided|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4B": 1,
    "Congenital_myasthenic_syndrome_4A|Congenital_myasthenic_syndrome_4C|not_provided|Congenital_myasthenic_syndrome_4B": 1,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|not_provided": 1,
    "Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Pseudo_von_Willebrand_disease|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 11,
    "GP1BA-related_disorder|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 1,
    "Bernard_Soulier_syndrome|Pseudo_von_Willebrand_disease|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|not_provided": 1,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 11,
    "Bernard_Soulier_syndrome|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Pseudo_von_Willebrand_disease|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|not_specified|not_provided": 1,
    "Bernard_Soulier_syndrome|Inborn_genetic_diseases|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 1,
    "GP1BA-related_disorder": 29,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|GP1BA-related_disorder": 1,
    "GP1BA-related_disorder|Macrothrombocytopenia|not_specified": 1,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Bernard_Soulier_syndrome|not_provided|not_specified": 1,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Macrothrombocytopenia": 1,
    "Bernard_Soulier_syndrome|GP1BA-related_disorder|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Pseudo_von_Willebrand_disease|not_specified": 1,
    "not_provided|GP1BA-related_disorder": 2,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Thrombocytopenia": 1,
    "Bernard_Soulier_syndrome|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Pseudo_von_Willebrand_disease": 2,
    "not_specified|Pseudo_von_Willebrand_disease": 1,
    "GP1BA-related_disorder|not_specified": 2,
    "not_provided|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 1,
    "Thrombocytopenia|Macrothrombocytopenia|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 1,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Bernard_Soulier_syndrome": 1,
    "not_provided|Bernard_Soulier_syndrome|not_specified": 1,
    "Pseudo_von_Willebrand_disease|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Bernard_Soulier_syndrome|not_provided|Bernard-Soulier_syndrome|_type_A1": 1,
    "Pseudo_von_Willebrand_disease": 7,
    "not_provided|Bernard_Soulier_syndrome|Pseudo_von_Willebrand_disease|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to": 1,
    "Macrothrombocytopenia|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|not_provided|GP1BA-related_disorder": 1,
    "Bernard-Soulier_syndrome|_type_A1|not_provided|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 1,
    "Pseudo_von_Willebrand_disease|Impaired_ristocetin-induced_platelet_aggregation|not_provided|Thrombocytopenia": 1,
    "not_specified|GP1BA-related_disorder": 1,
    "Bernard-Soulier_syndrome|_type_A1": 2,
    "not_provided|GP1BA-related_disorder|not_specified": 1,
    "not_provided|Bernard_Soulier_syndrome|GP1BA-related_disorder": 1,
    "PLATELET_GLYCOPROTEIN_Ib_POLYMORPHISM|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to": 1,
    "GP1BA-related_disorder|not_provided": 4,
    "Thrombocytopenia|Abnormal_bleeding|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant": 1,
    "GP1BA-related_disorder|CIC-rearranged_sarcoma|not_specified|not_provided": 1,
    "not_specified|not_provided|Bernard_Soulier_syndrome|Inborn_genetic_diseases": 1,
    "GP1BA-related_disorder|Bernard_Soulier_syndrome|Pseudo_von_Willebrand_disease|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|not_specified|not_provided": 1,
    "Bernard_Soulier_syndrome|Pseudo_von_Willebrand_disease|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to": 1,
    "GP1BA-related_disorder|Bernard_Soulier_syndrome|Pseudo_von_Willebrand_disease|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|not_provided": 1,
    "Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Bernard_Soulier_syndrome|Pseudo_von_Willebrand_disease|not_provided|Bernard-Soulier_syndrome|_type_A1": 1,
    "Bernard_Soulier_syndrome|GP1BA-related_disorder": 1,
    "Inborn_genetic_diseases|GP1BA-related_disorder": 1,
    "not_specified|not_provided|Thrombocytopenia|Abnormal_bleeding|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Bernard_Soulier_syndrome|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Pseudo_von_Willebrand_disease": 1,
    "Pseudo_von_Willebrand_disease|Inborn_genetic_diseases": 1,
    "not_provided|Bernard_Soulier_syndrome|not_specified|Pseudo_von_Willebrand_disease|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to|Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|GP1BA-related_disorder": 1,
    "Bernard-Soulier_syndrome|_type_A2|_autosomal_dominant|Pseudo_von_Willebrand_disease|Bernard_Soulier_syndrome|Nonarteritic_anterior_ischemic_optic_neuropathy|_susceptibility_to": 1,
    "Pheochromocytoma/paraganglioma_syndrome_6|not_provided|not_specified": 1,
    "Pheochromocytoma/paraganglioma_syndrome_6": 6,
    "SLC25A11-related_disorder": 4,
    "not_provided|SLC25A11-related_disorder": 1,
    "PFN1-related_disorder": 6,
    "not_provided|PFN1-related_disorder": 1,
    "not_provided|PFN1-related_disorder|not_specified": 1,
    "PFN1-related_disorder|not_provided": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_18": 2,
    "not_provided|Amyotrophic_lateral_sclerosis_type_18|not_specified": 2,
    "not_provided|PFN1-related_disorder|Amyotrophic_lateral_sclerosis_type_18": 1,
    "Amyotrophic_lateral_sclerosis_type_18|Neurodegeneration": 1,
    "PFN1-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_18": 1,
    "Amyotrophic_lateral_sclerosis_type_18": 1,
    "Amyotrophic_lateral_sclerosis|not_provided": 1,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 243,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|not_specified|not_provided": 4,
    "Inborn_genetic_diseases|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 11,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|not_provided": 8,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|not_specified": 3,
    "not_specified|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 3,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|Inborn_genetic_diseases": 12,
    "not_provided|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 6,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|ENO3-related_disorder|not_specified": 2,
    "not_provided|not_specified|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 3,
    "not_provided|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|not_specified": 4,
    "ENO3-related_disorder|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 2,
    "not_specified|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|ENO3-related_disorder": 1,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|ENO3-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 1,
    "Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|ENO3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|ENO3-related_disorder|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 1,
    "not_specified|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|not_provided": 1,
    "not_specified|not_provided|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency": 2,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_due_to_muscle_beta-enolase_deficiency|ENO3-related_disorder": 1,
    "Inborn_genetic_diseases|Spastic_ataxia_2": 29,
    "Spastic_ataxia_2": 329,
    "Hereditary_spastic_paraplegia|not_provided|Spastic_ataxia_2": 4,
    "Inborn_genetic_diseases|not_provided|Spastic_ataxia_2": 1,
    "not_provided|Spastic_ataxia_2|Inborn_genetic_diseases": 2,
    "Spastic_ataxia_2|not_specified|Hereditary_spastic_paraplegia": 1,
    "Spastic_ataxia_2|Hereditary_spastic_paraplegia": 3,
    "not_provided|Spastic_ataxia_2": 16,
    "not_specified|Spastic_ataxia_2|not_provided": 3,
    "Spastic_ataxia_2|Inborn_genetic_diseases": 10,
    "Hereditary_spastic_paraplegia|Spastic_ataxia_2|not_provided": 3,
    "Hereditary_spastic_paraplegia|Spastic_ataxia_2": 8,
    "Spastic_ataxia_2|not_provided": 24,
    "KIF1C-related_disorder": 3,
    "Spastic_ataxia_2|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Microcephaly|Spastic_ataxia_2": 1,
    "Spastic_ataxia_2|not_provided|Hereditary_spastic_paraplegia": 7,
    "not_provided|Hereditary_spastic_paraplegia|Spastic_ataxia_2": 3,
    "not_specified|Spastic_ataxia_2": 7,
    "Spastic_ataxia_2|not_specified": 5,
    "KIF1C-related_disorder|Spastic_ataxia_2": 3,
    "KIF1C-related_disorder|Inborn_genetic_diseases|Spastic_ataxia_2|not_provided|Hereditary_spastic_paraplegia": 1,
    "not_provided|Spastic_ataxia_2|not_specified": 2,
    "Spastic_ataxia_2|not_provided|not_specified": 1,
    "Spastic_ataxia_2|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "Spastic_ataxia_2|Hereditary_spastic_paraplegia|not_specified": 1,
    "Inborn_genetic_diseases|Spastic_ataxia_2|Hereditary_spastic_paraplegia": 2,
    "not_provided|Hereditary_spastic_paraplegia|not_specified|Spastic_ataxia_2": 3,
    "Spastic_ataxia_2|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Spastic_ataxia_2|KIF1C-related_disorder": 2,
    "Inborn_genetic_diseases|Spastic_ataxia_2|not_provided": 2,
    "not_specified|not_provided|Spastic_ataxia_2|Hereditary_spastic_paraplegia": 1,
    "not_specified|Spastic_ataxia_2|not_provided|Hereditary_spastic_paraplegia": 2,
    "not_specified|not_provided|Spastic_ataxia_2": 2,
    "Spastic_ataxia_2|not_specified|not_provided": 1,
    "KIF1C-related_disorder|Spastic_ataxia_2|not_provided|Hereditary_spastic_paraplegia": 2,
    "Spastic_ataxia_2|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_ataxia_2|not_provided|KIF1C-related_disorder|Hereditary_spastic_paraplegia": 2,
    "Spastic_ataxia_2|Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Spastic_ataxia_2": 1,
    "KIF1C-related_disorder|not_provided|Spastic_ataxia_2": 1,
    "KIF1C-related_disorder|not_provided|Spastic_ataxia_2|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|not_provided|Spastic_ataxia_2": 1,
    "not_specified|Hereditary_spastic_paraplegia|Spastic_ataxia_2|Inborn_genetic_diseases": 1,
    "KIF1C-related_disorder|not_specified|Spastic_ataxia_2": 1,
    ".|SLC52A1-related_disorder|not_provided": 3,
    "Ariboflavinosis": 7,
    ".|Ariboflavinosis": 2,
    "not_specified|Ariboflavinosis": 1,
    "Ariboflavinosis|not_provided|.|not_specified": 1,
    "not_provided|Ariboflavinosis|.": 1,
    ".|Maternal_riboflavin_deficiency": 1,
    "Ariboflavinosis|.|not_provided": 2,
    "Ariboflavinosis|not_specified": 1,
    "SLC52A1-related_disorder|.": 1,
    "Ariboflavinosis|.|not_specified": 1,
    "Maternal_riboflavin_deficiency|Ariboflavinosis": 1,
    ".|not_provided|Ariboflavinosis|SLC52A1-related_disorder": 1,
    "Ariboflavinosis|not_provided|.": 1,
    "SLC52A1-related_disorder|not_provided": 1,
    "not_provided|NUP88-related_disorder": 1,
    "not_provided|Fetal_akinesia_deformation_sequence_4": 4,
    "Fetal_akinesia_deformation_sequence_4|not_provided": 5,
    "Fetal_akinesia_deformation_sequence_4": 5,
    "NUP88-related_disorder": 13,
    "Fetal_akinesia_deformation_sequence_4|not_specified": 2,
    "not_specified|Fetal_akinesia_deformation_sequence_4": 1,
    "Combined_oxidative_phosphorylation_deficiency_33": 5,
    "C1QBP-related_disorder|not_provided": 8,
    "not_provided|Mitochondrial_disease|Combined_oxidative_phosphorylation_deficiency_33": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_33": 2,
    "Combined_oxidative_phosphorylation_deficiency_33|not_provided": 1,
    "not_provided|C1QBP-related_disorder": 4,
    "C1QBP-related_disorder": 2,
    "Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome": 6,
    "NLRP1-related_disorder|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|NLRP1-related_disorder": 1,
    "not_provided|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Inborn_genetic_diseases": 1,
    "not_provided|NLRP1-related_disorder": 18,
    "NLRP1-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "Autoinflammation_with_arthritis_and_dyskeratosis|not_provided": 3,
    "not_provided|Autoinflammation_with_arthritis_and_dyskeratosis": 3,
    "Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Autoinflammation_with_arthritis_and_dyskeratosis|not_provided|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|not_specified": 1,
    "not_provided|Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome": 1,
    "Autoinflammation_with_arthritis_and_dyskeratosis|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|not_provided": 1,
    "Respiratory_papillomatosis|_juvenile_recurrent|_congenital": 2,
    "Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1": 1,
    "Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|not_provided": 3,
    "not_provided|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|Autoinflammation_with_arthritis_and_dyskeratosis": 1,
    "Autoinflammation_with_arthritis_and_dyskeratosis": 3,
    "NLRP1-related_disorder|not_provided|Autoinflammation_with_arthritis_and_dyskeratosis": 1,
    "NLRP1-related_disorder": 6,
    "not_specified|not_provided|NLRP1-related_disorder": 1,
    "not_provided|Autoinflammation_with_arthritis_and_dyskeratosis|Inborn_genetic_diseases": 1,
    "Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "NLRP1-related_disorder|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|not_provided": 1,
    "Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|not_specified|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|not_provided": 1,
    "NLRP1-related_disorder|not_specified": 1,
    "Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Autoinflammation_with_arthritis_and_dyskeratosis|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|not_provided": 2,
    "Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Autoinflammation_with_arthritis_and_dyskeratosis|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|not_provided": 1,
    "Autoinflammation_with_arthritis_and_dyskeratosis|Vitiligo-associated_multiple_autoimmune_disease_susceptibility_1|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome|not_provided|NLRP1-related_disorder": 1,
    "not_provided|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome": 1,
    "NLRP1-related_disorder|Respiratory_papillomatosis|_juvenile_recurrent|_congenital|Autoinflammation_with_arthritis_and_dyskeratosis|not_provided|not_specified|Corneal_intraepithelial_dyskeratosis-palmoplantar_hyperkeratosis-laryngeal_dyskeratosis_syndrome": 1,
    "Leber_congenital_amaurosis_4": 325,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_4": 7,
    "not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_4": 6,
    "not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis_4": 3,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis_4": 7,
    "Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis_4": 3,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 13,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis": 3,
    "Leber_congenital_amaurosis_4|Retinitis_pigmentosa": 6,
    "not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis_4": 2,
    "Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Dominant|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis_4|Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant": 6,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant": 1,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Dominant|not_provided|Retinitis_Pigmentosa|_Recessive": 1,
    "Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant|not_provided": 3,
    "Leber_congenital_amaurosis_4|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant": 5,
    "Leber_congenital_amaurosis_4|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive": 2,
    "not_provided|Leber_congenital_amaurosis_4|Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant": 2,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_4": 11,
    "AIPL1-related_retinopathy": 6,
    "Retinitis_Pigmentosa|_Dominant|AIPL1-related_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_4|Retinitis_pigmentosa|not_specified|not_provided": 1,
    "Leber_congenital_amaurosis_4|Inborn_genetic_diseases": 4,
    "Leber_congenital_amaurosis_4|AIPL1-related_disorder": 6,
    "not_provided|Leber_congenital_amaurosis_4|Retinitis_pigmentosa|Retinal_dystrophy|Inborn_genetic_diseases|Retinitis_Pigmentosa|_Dominant": 1,
    "not_provided|Leber_congenital_amaurosis_4|Retinitis_pigmentosa|AIPL1-related_retinopathy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis_4|AIPL1-related_retinopathy|not_provided|Retinal_dystrophy": 1,
    "not_specified|Leber_congenital_amaurosis_4|Juvenile_retinitis_pigmentosa|_AIPL1-related|CONE-ROD_DYSTROPHY|_AIPL1-RELATED|not_provided|Retinitis_pigmentosa|AIPL1-related_disorder|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Inborn_genetic_diseases|Leber_congenital_amaurosis_4": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis_4": 1,
    "not_provided|Leber_congenital_amaurosis_4": 6,
    "AIPL1-related_retinopathy|not_provided|Leber_congenital_amaurosis_4": 3,
    "AIPL1-related_retinopathy|AIPL1-related_disorder|Retinal_dystrophy|not_specified|not_provided|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis_4|not_specified": 2,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis_4|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "AIPL1-related_retinopathy|not_provided|not_specified|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_retinopathy|Inborn_genetic_diseases": 1,
    "Myopia_25|_autosomal_dominant|AIPL1-related_disorder|not_specified|not_provided|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis_4|Inborn_genetic_diseases": 1,
    "Leber_congenital_amaurosis_4|AIPL1-related_disorder|AIPL1-related_retinopathy": 1,
    "AIPL1-related_disorder|AIPL1-related_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_4|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_4|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis|not_specified": 1,
    "Leber_congenital_amaurosis_4|AIPL1-related_retinopathy|Leber_congenital_amaurosis": 1,
    "not_provided|Leber_congenital_amaurosis_4|AIPL1-related_retinopathy": 1,
    "AIPL1-related_disorder|Retinal_dystrophy": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_4": 2,
    "Leber_congenital_amaurosis_4|AIPL1-related_disorder|CONE-ROD_DYSTROPHY|_AIPL1-RELATED|Juvenile_retinitis_pigmentosa|_AIPL1-related|AIPL1-related_retinopathy|not_provided": 1,
    "AIPL1-related_disorder|Leber_congenital_amaurosis_4": 2,
    "Fraser_syndrome_3|Leber_congenital_amaurosis_4": 1,
    "not_specified|Leber_congenital_amaurosis_4": 2,
    "Retinitis_Pigmentosa|_Dominant|not_provided|Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis_4|AIPL1-related_retinopathy": 5,
    "Inborn_genetic_diseases|AIPL1-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Dominant|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis_4": 2,
    "AIPL1-related_retinopathy|not_provided|Leber_congenital_amaurosis|Leber_congenital_amaurosis_4": 2,
    "AIPL1-related_disorder|Retinitis_pigmentosa|Leber_congenital_amaurosis_4|Inborn_genetic_diseases": 1,
    "Retinitis_Pigmentosa|_Dominant|AIPL1-related_retinopathy|not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_4": 3,
    "not_provided|AIPL1-related_retinopathy": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_4|not_provided": 1,
    "AIPL1-related_disorder|Leber_congenital_amaurosis_4|AIPL1-related_retinopathy|Inborn_genetic_diseases": 1,
    "AIPL1-related_disorder|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_disorder|Inborn_genetic_diseases|Leber_congenital_amaurosis_4": 2,
    "Leber_congenital_amaurosis_4|not_provided": 2,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis|AIPL1-related_retinopathy|Leber_congenital_amaurosis_4": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_4|Retinitis_Pigmentosa|_Recessive": 1,
    "AIPL1-related_retinopathy|not_provided|not_specified|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_disorder|Leber_congenital_amaurosis_4|not_provided|AIPL1-related_retinopathy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_4|Retinitis_Pigmentosa|_Recessive|not_specified": 1,
    "Leber_congenital_amaurosis_4|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_4|AIPL1-related_disorder|Inborn_genetic_diseases": 1,
    "AIPL1-related_retinopathy|Inborn_genetic_diseases|Leber_congenital_amaurosis_4": 2,
    "Retinitis_Pigmentosa|_Recessive|AIPL1-related_retinopathy|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_4": 1,
    "not_provided|Retinitis_pigmentosa|Retinitis_Pigmentosa|_Recessive|not_specified|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis_4|Cone-rod_dystrophy_2|Retinitis_pigmentosa": 1,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis_4|Retinitis_pigmentosa|not_specified|not_provided|Lissencephaly_due_to_TUBA1A_mutation": 1,
    "Inborn_genetic_diseases|AIPL1-related_retinopathy|not_provided|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis_4|not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|Retinitis_Pigmentosa|_Recessive|Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis_4|Retinitis_pigmentosa": 1,
    "Retinitis_Pigmentosa|_Dominant|not_provided|AIPL1-related_retinopathy|not_specified|Retinitis_pigmentosa|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis_4": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant|not_specified|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 1,
    "Retinal_dystrophy|Leber_congenital_amaurosis_4": 1,
    "not_specified|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_4": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_4|not_provided": 1,
    "Leber_congenital_amaurosis|Leber_congenital_amaurosis_4|AIPL1-related_retinopathy": 2,
    "AIPL1-related_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_retinopathy|not_provided|Leber_congenital_amaurosis_4|Retinal_dystrophy": 1,
    "AIPL1-related_retinopathy|Leber_congenital_amaurosis_4|not_provided": 1,
    "Leber_congenital_amaurosis_4|not_provided|not_specified": 1,
    "not_specified|AIPL1-related_retinopathy|not_provided|Leber_congenital_amaurosis_4": 1,
    "Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant|not_provided|AIPL1-related_retinopathy|Leber_congenital_amaurosis_4": 1,
    "Retinitis_Pigmentosa|_Dominant|not_provided|Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_4|not_specified": 1,
    "Retinitis_pigmentosa|AIPL1-related_retinopathy|Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis_4": 1,
    "AIPL1-related_retinopathy|not_provided": 1,
    "Retinitis_Pigmentosa|_Dominant|Retinitis_Pigmentosa|_Recessive|not_specified|Leber_congenital_amaurosis_4": 1,
    "Retinitis_Pigmentosa|_Recessive|Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Dominant": 3,
    "not_provided|Leber_congenital_amaurosis|Retinitis_Pigmentosa|_Recessive|Retinitis_Pigmentosa|_Dominant": 1,
    "Cone-rod_dystrophy_5": 85,
    "Cone-rod_dystrophy_5|not_provided": 32,
    "not_provided|Cone-rod_dystrophy_5": 17,
    "PITPNM3-related_disorder": 3,
    "not_provided|PITPNM3-related_disorder": 4,
    "PITPNM3-related_disorder|not_provided": 5,
    "not_provided|Cone-rod_dystrophy_5|not_specified": 6,
    "not_specified|not_provided|Cone-rod_dystrophy_5": 5,
    "not_provided|not_specified|Cone-rod_dystrophy_5": 5,
    "Cone-rod_dystrophy_5|PITPNM3-related_disorder|not_provided": 1,
    "PITPNM3-related_disorder|Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_5": 1,
    "Cone-rod_dystrophy_5|Retinitis_pigmentosa|not_provided": 1,
    "PITPNM3-related_disorder|not_specified|Cone-rod_dystrophy_5|not_provided": 1,
    "not_provided|PITPNM3-related_disorder|Cone-rod_dystrophy_5": 1,
    "PITPNM3-related_disorder|not_provided|Cone-rod_dystrophy_5": 2,
    "not_specified|Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_5": 1,
    "PITPNM3-related_disorder|Cone-rod_dystrophy_5|not_provided": 1,
    "not_specified|Cone-rod_dystrophy_5|not_provided": 1,
    "not_specified|Cone-rod_dystrophy_5|PITPNM3-related_disorder|not_provided": 1,
    "Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|not_provided|Joubert_syndrome_38": 1,
    "Orofaciodigital_syndrome_XV|not_provided|Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly": 2,
    "not_provided|KIAA0753-related_disorder": 7,
    "Short-rib_thoracic_dysplasia_21_without_polydactyly": 2,
    "KIAA0753-related_disorder|not_provided": 3,
    "Orofaciodigital_syndrome_XV|Short-rib_thoracic_dysplasia_21_without_polydactyly|KIAA0753-related_disorder|not_provided": 1,
    "Joubert_syndrome_38": 3,
    "Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|not_provided": 2,
    "Orofaciodigital_syndrome_XV|not_provided|Joubert_syndrome_38|not_specified": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|not_provided": 1,
    "Orofaciodigital_syndrome_XV|Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|not_provided": 1,
    "KIAA0753-related_disorder": 1,
    "not_specified|not_provided|Short-rib_thoracic_dysplasia_21_without_polydactyly": 1,
    "Orofaciodigital_syndrome_XV|not_provided|Joubert_syndrome_38": 1,
    "Joubert_syndrome_38|not_provided": 1,
    "Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|not_provided|Orofaciodigital_syndrome_XV": 2,
    "Short-rib_thoracic_dysplasia_21_without_polydactyly|Jeune_thoracic_dystrophy|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV": 1,
    "Orofaciodigital_syndrome_XV|Short-rib_thoracic_dysplasia_21_without_polydactyly|not_provided|Jeune_thoracic_dystrophy|Joubert_syndrome": 1,
    "not_provided|Short-rib_thoracic_dysplasia_21_without_polydactyly|Jeune_thoracic_dystrophy|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|Jeune_thoracic_dystrophy|Joubert_syndrome": 1,
    "Inborn_genetic_diseases|Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|not_provided": 1,
    "KIAA0753-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|KIAA0753-related_disorder": 1,
    "Inborn_genetic_diseases|Orofaciodigital_syndrome_XV|not_provided": 1,
    "not_provided|Short-rib_thoracic_dysplasia_21_without_polydactyly|Joubert_syndrome_38|Orofaciodigital_syndrome_XV": 1,
    "Joubert_syndrome_38|Short-rib_thoracic_dysplasia_21_without_polydactyly|Orofaciodigital_syndrome_XV|not_provided|KIAA0753-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_25": 463,
    "Developmental_and_epileptic_encephalopathy|_25|not_provided": 25,
    "not_specified|Developmental_and_epileptic_encephalopathy|_25": 5,
    "Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases": 6,
    "not_specified|Developmental_and_epileptic_encephalopathy|_25|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_25|not_provided": 11,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_25": 30,
    "not_provided|Developmental_and_epileptic_encephalopathy|_25": 30,
    "Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_25|not_specified": 17,
    "Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_25": 6,
    "Developmental_and_epileptic_encephalopathy|_25|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_25|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_25|SLC13A5-related_disorder": 1,
    "SLC13A5-related_disorder|Developmental_and_epileptic_encephalopathy|_25": 3,
    "Developmental_and_epileptic_encephalopathy|_25|not_specified|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_25": 4,
    "not_specified|Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_25|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_25|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_25|SLC13A5-related_disorder|not_provided": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_25": 1,
    "Inborn_genetic_diseases|not_provided|SLC13A5-related_disorder|Developmental_and_epileptic_encephalopathy|_25": 1,
    "Developmental_and_epileptic_encephalopathy|_25|not_provided|Undetermined_early-onset_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_25|SLC13A5-related_disorder": 1,
    "Microcephaly|Developmental_and_epileptic_encephalopathy|_25|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_25|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_25|not_provided|Intellectual_disability": 1,
    "SLC13A5-related_disorder": 1,
    "Inborn_genetic_diseases|See_cases|Developmental_and_epileptic_encephalopathy|_25": 1,
    "SLC13A5-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_25|not_provided": 1,
    "Global_developmental_delay|Seizure|Chronic_kidney_disease": 1,
    "SLC13A5-related_disorder|Developmental_and_epileptic_encephalopathy|_25|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases|SLC13A5-related_disorder|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_25|Inborn_genetic_diseases": 1,
    "TEKT1-related_disorder": 2,
    "ALOX12-related_condition": 1,
    "Short_stature_with_nonspecific_skeletal_abnormalities_1": 1,
    "DLG4-related_disorder|not_provided": 4,
    "Intellectual_developmental_disorder_62": 83,
    "DLG4-related_disorder": 10,
    "DLG4-related_synaptopathy": 1,
    "Intellectual_developmental_disorder_62|DLG4-related_disorder": 1,
    "DLG4-related_disorder|not_specified|not_provided": 1,
    "Marfanoid_habitus_and_intellectual_disability|Intellectual_developmental_disorder_62": 3,
    "Neurodevelopmental_delay|Intellectual_developmental_disorder_62": 1,
    "not_provided|Intellectual_developmental_disorder_62": 4,
    "Intellectual_developmental_disorder_62|not_provided": 12,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_62|not_provided": 2,
    "Intellectual_disability|Neurodevelopmental_delay": 8,
    "DLG4-related_disorder|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_62|DLG4-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_62": 2,
    "Intellectual_developmental_disorder_62|not_provided|DLG4-related_disorder": 1,
    "Intellectual_disability-epilepsy-extrapyramidal_syndrome|Intellectual_disability|_autosomal_dominant_24": 1,
    "Inborn_genetic_diseases|DLG4-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder_62|Cerebral_visual_impairment_and_intellectual_disability": 1,
    "ACADVL-related_disorder": 8,
    "not_provided|Primary_familial_hypertrophic_cardiomyopathy|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|DLG4-related_disorder": 1,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 99,
    "not_specified|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 17,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided": 44,
    "ACADVL-related_disorder|not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 2,
    "Rhabdomyolysis|Abnormal_circulating_enzyme_concentration|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 9,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 1,
    "ACADVL-related_disorder|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 7,
    "not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 28,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder": 13,
    "ACADVL-related_disorder|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 7,
    "Inborn_genetic_diseases|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 25,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 16,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified": 4,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified": 28,
    "not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "ACADVL-related_disorder|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided": 4,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Pearson_syndrome|Inborn_genetic_diseases": 1,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder|not_provided": 3,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 4,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder|Inborn_genetic_diseases": 1,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided": 6,
    "ACADVL-related_disorder|Inborn_genetic_diseases|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 3,
    "not_provided|not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 4,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder|not_provided": 1,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder|not_specified": 1,
    "not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder": 1,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|See_cases": 1,
    "ACADVL-related_disorder|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "ACADVL-related_disorder|not_provided": 1,
    "ACADVL-related_disorder|Inborn_genetic_diseases|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|See_cases": 1,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Abnormality_of_the_musculature": 2,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "Abnormality_of_the_musculature|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|Cardiac_arrhythmia": 1,
    "not_provided|not_specified|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder": 1,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder": 3,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_provided|not_specified": 2,
    "Rhabdomyolysis|Abnormal_circulating_enzyme_concentration|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|Myopathy|Rhabdomyolysis|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|ACADVL-related_disorder|not_provided|Myopathy|Rhabdomyolysis|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 3,
    "not_provided|ACADVL-related_disorder|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 2,
    "Inborn_genetic_diseases|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Primary_dilated_cardiomyopathy|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency|ACADVL-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|ACADVL-related_disorder|not_provided|Inborn_genetic_diseases|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "ACADVL-related_disorder|not_specified|not_provided|Very_long_chain_acyl-CoA_dehydrogenase_deficiency": 1,
    "Very_long_chain_acyl-CoA_dehydrogenase_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "DVL2-related_disorder": 11,
    "not_provided|DVL2-related_disorder": 1,
    "Faundes-Banka_syndrome|EIF5A-related_disorder": 1,
    "Faundes-Banka_syndrome": 7,
    "EIF5A-related_disorder": 1,
    "not_provided|Faundes-Banka_syndrome": 1,
    "Faundes-Banka_syndrome|not_provided": 1,
    "NEURL4-related_disorder": 1,
    "TNK1-related_disorder": 15,
    "TNK1-related_disorder|not_provided": 1,
    "not_provided|TNK1-related_disorder": 2,
    "NLGN2-related_disorder": 7,
    "Congenital_myasthenic_syndrome_4C|CHRNB1-related_disorder|not_specified": 1,
    "Congenital_myasthenic_syndrome_2A|not_provided": 21,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_2A": 15,
    "not_provided|Congenital_myasthenic_syndrome_2A": 12,
    "Congenital_myasthenic_syndrome_2A": 271,
    "Congenital_myasthenic_syndrome_2A|Inborn_genetic_diseases": 10,
    "Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_4C": 6,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_2A": 3,
    "CHRNB1-related_disorder|Congenital_myasthenic_syndrome_2A": 5,
    "Congenital_Myasthenic_Syndrome|_Dominant/Recessive|Congenital_myasthenic_syndrome_2A": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_2A": 1,
    "not_provided|Congenital_myasthenic_syndrome_2A|not_specified|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_2A|not_specified|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_2A|not_provided|Congenital_myasthenic_syndrome_4C": 1,
    "CHRNB1-related_disorder": 3,
    "Congenital_myasthenic_syndrome_4C|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_2A": 1,
    "Congenital_myasthenic_syndrome_2A|not_provided|Congenital_myasthenic_syndrome_4C|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_2A": 1,
    "Congenital_myasthenic_syndrome_2A|not_provided|Inborn_genetic_diseases": 3,
    "Congenital_myasthenic_syndrome_2C": 2,
    "Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_2C|not_provided": 2,
    "Congenital_myasthenic_syndrome_2A|not_provided|Congenital_myasthenic_syndrome_4C": 2,
    "Congenital_myasthenic_syndrome_2A|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Congenital_myasthenic_syndrome_2C|Congenital_myasthenic_syndrome_2A": 1,
    "Congenital_myasthenic_syndrome_4C|CHRNB1-related_disorder|Congenital_myasthenic_syndrome_2A": 1,
    "Congenital_myasthenic_syndrome_2A|not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_2A|not_specified|Congenital_myasthenic_syndrome_4C|not_provided": 3,
    "Congenital_myasthenic_syndrome_2A|See_cases": 2,
    "Congenital_myasthenic_syndrome_2A|not_specified": 2,
    "Congenital_myasthenic_syndrome_2A|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4C": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_2A": 2,
    "Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_2A|not_specified": 1,
    "not_specified|Congenital_myasthenic_syndrome_2A": 3,
    "Congenital_myasthenic_syndrome_2A|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_4C": 1,
    "CHRNB1-related_disorder|Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_4C|not_provided": 2,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_2A|not_provided": 1,
    "not_provided|Congenital_myasthenic_syndrome_2A|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_4C|Congenital_myasthenic_syndrome_2A": 1,
    "CHRNB1-related_disorder|Congenital_myasthenic_syndrome_4C|not_specified|Congenital_myasthenic_syndrome_2A": 1,
    "Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_2C|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome_2A|not_provided|not_specified|Congenital_myasthenic_syndrome_4C": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_2C": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_2A": 1,
    "See_cases|Congenital_myasthenic_syndrome_2A|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_2A|CHRNB1-related_disorder": 1,
    "Congenital_myasthenic_syndrome_2A|not_provided|Congenital_myasthenic_syndrome_2C|Congenital_myasthenic_syndrome_4C": 1,
    "Congenital_myasthenic_syndrome_4C|not_provided|not_specified": 1,
    "not_provided|Congenital_myasthenic_syndrome_4C": 3,
    "POLR2A-related_disorder": 19,
    "Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities|not_provided": 9,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities": 4,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities": 3,
    "Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities|Inborn_genetic_diseases": 4,
    "POLR2A-related_disorder|not_provided": 3,
    "not_provided|POLR2A-related_disorder": 5,
    "not_provided|Severe_global_developmental_delay": 1,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities|Inborn_genetic_diseases": 1,
    "Gemcitabine_response": 1,
    "POLR2A-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities|Neurodevelopmental_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia_and_variable_intellectual_and_behavioral_abnormalities": 1,
    "Inborn_genetic_diseases|POLR2A-related_disorder": 1,
    "Common_variable_immunodeficiency|Immunodeficiency|_common_variable|_10|not_provided|See_cases": 1,
    "not_provided|Common_variable_immunodeficiency": 4,
    "Common_variable_immunodeficiency|TNFSF12-related_disorder": 2,
    "not_provided|Common_variable_immunodeficiency|not_specified": 1,
    "TNFSF12-related_disorder|Common_variable_immunodeficiency": 3,
    "TNFSF12-related_disorder|Common_variable_immunodeficiency|not_provided": 2,
    "not_specified|not_provided|Common_variable_immunodeficiency": 2,
    "Common_variable_immunodeficiency|not_provided|TNFSF12-related_disorder": 1,
    "Common_variable_immunodeficiency|not_specified": 3,
    "TNFSF12-related_disorder|not_specified|Common_variable_immunodeficiency|not_provided": 1,
    "not_specified|Common_variable_immunodeficiency": 2,
    "not_specified|Congenital_disorder_of_glycosylation": 8,
    "MPDU1-congenital_disorder_of_glycosylation": 51,
    "not_specified|MPDU1-congenital_disorder_of_glycosylation": 3,
    "Inborn_genetic_diseases|MPDU1-congenital_disorder_of_glycosylation": 3,
    "MPDU1-related_disorder": 1,
    "not_specified|not_provided|MPDU1-congenital_disorder_of_glycosylation": 3,
    "MPDU1-related_disorder|MPDU1-congenital_disorder_of_glycosylation|not_specified": 2,
    "MPDU1-congenital_disorder_of_glycosylation|not_provided": 4,
    "not_provided|MPDU1-congenital_disorder_of_glycosylation": 3,
    "not_provided|MPDU1-congenital_disorder_of_glycosylation|not_specified": 1,
    "Inborn_genetic_diseases|MPDU1-congenital_disorder_of_glycosylation|not_provided": 1,
    "MPDU1-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "MPDU1-related_disorder|MPDU1-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "SHBG-related_disorder": 3,
    "not_provided|SHBG-related_disorder": 1,
    "Sex_Hormone-Binding_Globulin_Deficiency": 1,
    "not_provided|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 3,
    "TP53-related_disorder": 8,
    "Li-Fraumeni_syndrome": 775,
    "not_provided|Li-Fraumeni_syndrome": 15,
    "TP53-related_disorder|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Basal_cell_carcinoma|_susceptibility_to|_7": 1,
    "Li-Fraumeni_syndrome_1|not_provided": 3,
    "Li-Fraumeni_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|Li-Fraumeni_syndrome_1": 3,
    "B-cell_chronic_lymphocytic_leukemia": 1,
    "not_specified|Li-Fraumeni_syndrome_1": 2,
    "Li-Fraumeni_syndrome_1|Familial_pancreatic_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 7,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 50,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 284,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 70,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 196,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 83,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 17,
    "Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 28,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 5,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 4,
    "Adrenocortical_carcinoma|_hereditary|Basal_cell_carcinoma|_susceptibility_to|_7|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Choroid_plexus_papilloma|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 74,
    "Adrenocortical_carcinoma|_hereditary": 17,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|not_provided": 5,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 20,
    "Familial_cancer_of_breast|Classic_Hodgkin_lymphoma|Ovarian_neoplasm|Thyroid_cancer|_nonmedullary|_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|TP53-related_disorder": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 14,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1": 2,
    "Adrenocortical_carcinoma|_hereditary|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Colorectal_cancer|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_provided|Li-Fraumeni_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 22,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 34,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1": 1,
    "not_specified|Li-Fraumeni_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 31,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Malignant_tumor_of_breast": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Diamond-Blackfan_anemia|Bone_marrow_failure_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 4,
    "Nasopharyngeal_carcinoma|Colorectal_cancer|Choroid_plexus_papilloma|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Bone_marrow_failure_syndrome_5|Glioma_susceptibility_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 19,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Diamond-Blackfan_anemia|Bone_marrow_failure_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|not_specified|not_provided|Li-Fraumeni_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 10,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_polyposis|Colonic_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Poly_(ADP-Ribose)_polymerase_inhibitor_response": 2,
    "Li-Fraumeni_syndrome_1|Lung_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Ovarian_neoplasm": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Ovarian_neoplasm|Li-Fraumeni_syndrome": 9,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 17,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 3,
    "Colonic_diverticula|Gallbladder_cancer|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Bone_marrow_failure_syndrome_5|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Bone_osteosarcoma|Li-Fraumeni_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_7|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Hepatocellular_carcinoma|Colorectal_cancer|TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_provided|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1": 1,
    "Hepatocellular_carcinoma|Familial_cancer_of_breast|Bone_marrow_failure_syndrome_5|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Adrenocortical_carcinoma|_hereditary|Colorectal_cancer|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Nasopharyngeal_carcinoma|TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Breast_neoplasm|not_provided|ADRENOCORTICAL_CARCINOMA|_PEDIATRIC|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 3,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 4,
    "Adrenocortical_carcinoma|_hereditary|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Hepatocellular_carcinoma|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Glioma_susceptibility_1|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 24,
    "TP53-related_disorder|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|TP53-related_disorder|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|not_specified|Li-Fraumeni_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder": 2,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 1,
    "TP53-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|TP53-related_disorder": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "TP53-related_disorder|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|TP53-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|not_specified|Li-Fraumeni_syndrome_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Acute_myeloid_leukemia|Li-Fraumeni_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 6,
    "Adrenal_cortex_carcinoma|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|not_provided|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|TP53-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_provided|Li-Fraumeni_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 6,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|not_provided|Li-Fraumeni_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Non-Hodgkin_lymphoma|Li-Fraumeni_syndrome|Familial_colorectal_cancer": 1,
    "Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome": 3,
    "Sarcoma|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 15,
    "Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 6,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 3,
    "Li-Fraumeni_syndrome|Ovarian_neoplasm": 3,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|not_provided": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 3,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Breast_and/or_ovarian_cancer|not_provided|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 7,
    "not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 3,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 2,
    "Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|TP53-related_disorder|Li-Fraumeni_syndrome": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|not_specified|not_provided|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Lip_and_oral_cavity_carcinoma|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Lung_adenocarcinoma|Li-Fraumeni_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Lip_and_oral_cavity_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|not_provided": 3,
    "Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Carcinoma_of_colon|Malignant_tumor_of_breast": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Sarcoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Ovarian_neoplasm|Li-Fraumeni_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Basal_cell_carcinoma|_susceptibility_to|_7|Glioma_susceptibility_1|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Li-Fraumeni_syndrome_1|Colorectal_cancer|Familial_cancer_of_breast|Choroid_plexus_papilloma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Bone_marrow_failure_syndrome_5|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Bone_marrow_failure_syndrome_5|not_specified|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|not_specified": 1,
    "ADRENOCORTICAL_CARCINOMA|_PEDIATRIC|Choroid_plexus_carcinoma|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Poly_(ADP-Ribose)_polymerase_inhibitor_response": 1,
    "TP53-related_disorder|Astrocytoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Malignant_glioma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neoplasm_of_stomach|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 1,
    "Bone_osteosarcoma|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "TP53-related_disorder|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Pleomorphic_xanthoastrocytoma|Astrocytoma|_anaplastic|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Li-fraumeni-like_syndrome|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|Li-Fraumeni_syndrome|not_provided|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome": 6,
    "Malignant_tumor_of_breast|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome|Carcinoma_of_colon": 1,
    "Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Bone_osteosarcoma|Adrenocortical_carcinoma|_hereditary|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Glioma_susceptibility_1|Familial_cancer_of_breast|Basal_cell_carcinoma|_susceptibility_to|_7|Colorectal_cancer|Li-Fraumeni_syndrome_1|Bone_marrow_failure_syndrome_5|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary": 2,
    "Gallbladder_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Ovarian_neoplasm": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Nasopharyngeal_carcinoma|Malignant_tumor_of_urinary_bladder|Acute_myeloid_leukemia|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Gallbladder_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Bone_osteosarcoma|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Poly_(ADP-Ribose)_polymerase_inhibitor_response|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|TP53-related_disorder": 1,
    "Adrenocortical_carcinoma|_hereditary|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Acute_myeloid_leukemia|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast_carcinoma": 1,
    "Lip_and_oral_cavity_carcinoma|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 3,
    "Bone_osteosarcoma|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Li-Fraumeni_syndrome": 2,
    "Multiple_myeloma|Colorectal_cancer|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Familial_cancer_of_breast|Bone_marrow_failure_syndrome_5|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Adrenocortical_carcinoma|_hereditary|Choroid_plexus_papilloma|Nasopharyngeal_carcinoma|TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Rhabdomyosarcoma|Breast_and/or_ovarian_cancer|not_provided|Lung_adenocarcinoma|Thyroid_gland_undifferentiated_(anaplastic)_carcinoma|Ovarian_neoplasm|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Multiple_myeloma|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Prostate_cancer": 1,
    "TP53-related_disorder|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Basal_cell_carcinoma|_susceptibility_to|_7|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Bone_marrow_failure_syndrome_5|Hepatocellular_carcinoma|Colorectal_cancer|Glioma_susceptibility_1|Bone_osteosarcoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome|TP53-related_disorder": 1,
    "Li-Fraumeni_syndrome_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 2,
    "Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "TP53-related_disorder|Lip_and_oral_cavity_carcinoma|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Familial_cancer_of_breast|Bone_osteosarcoma|Carcinoma_of_colon|Basal_cell_carcinoma|_susceptibility_to|_7|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Prostate_cancer|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Lung_adenocarcinoma|Li-Fraumeni_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Atypical_endometrial_hyperplasia": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast": 1,
    "not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Squamous_cell_carcinoma_of_the_head_and_neck|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|not_provided|not_specified": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "Li-Fraumeni_syndrome|Bone_osteosarcoma|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Li-fraumeni-like_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Lung_sarcomatoid_carcinoma|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Acute_myeloid_leukemia|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_glioma|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Hepatocellular_carcinoma|Bone_osteosarcoma|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Basal_cell_carcinoma|_susceptibility_to|_7|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 4,
    "not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 2,
    "Acute_myeloid_leukemia|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome_1|Ovarian_neoplasm": 2,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Cervical_cancer|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Hepatocellular_carcinoma|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 4,
    "Bone_marrow_failure_syndrome_5|Choroid_plexus_papilloma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_osteosarcoma|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Colorectal_cancer|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Lymphoma|Lip_and_oral_cavity_carcinoma|TP53-related_disorder|Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Ductal_carcinoma_in_situ|Carcinoma_of_pancreas|Carcinoma_of_colon|Rhabdomyosarcoma|Sarcoma|not_provided|Multiple_myeloma|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Malignant_tumor_of_urinary_bladder|Li-Fraumeni_syndrome|Breast_carcinoma": 1,
    "Gallbladder_cancer|TP53-related_disorder|Congenital_fibrosarcoma|Lip_and_oral_cavity_carcinoma|Gastric_cancer|Breast_and/or_ovarian_cancer|Familial_pancreatic_carcinoma|Malignant_lymphoma|_large_B-cell|_diffuse|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Choroid_plexus_carcinoma|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Carcinoma_of_colon|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenal_cortex_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Atypical_teratoid_rhabdoid_tumor|Astrocytoma|_anaplastic|Nasopharyngeal_carcinoma|Adrenocortical_carcinoma|_hereditary|Bone_marrow_failure_syndrome_5|Hepatocellular_carcinoma|Bone_osteosarcoma|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Colorectal_cancer|Basal_cell_carcinoma|_susceptibility_to|_7|Carcinoma_of_pancreas|Choroid_plexus_papilloma|TP53-related_disorder|Familial_ovarian_cancer|Gastric_cancer|Adenocarcinoma|Hereditary_cancer-predisposing_syndrome|Li-fraumeni-like_syndrome|not_provided|Ovarian_neoplasm|Malignant_tumor_of_urinary_bladder|Li-Fraumeni_syndrome|Breast_carcinoma|See_cases": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 2,
    "Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-fraumeni-like_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "Adrenal_cortex_carcinoma": 1,
    "Lip_and_oral_cavity_carcinoma|Hepatocellular_carcinoma|Familial_cancer_of_breast|Bone_marrow_failure_syndrome_5|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Adrenocortical_carcinoma|_hereditary|Colorectal_cancer|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Nasopharyngeal_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hepatoblastoma|Li-Fraumeni_syndrome": 1,
    "Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Prostate_cancer": 1,
    "Gallbladder_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Ovarian_neoplasm|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Malignant_tumor_of_urinary_bladder|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Acute_myeloid_leukemia|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 1,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|TP53-related_disorder": 1,
    "not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|not_provided|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Ovarian_neoplasm": 2,
    "Ovarian_neoplasm|TP53-related_disorder": 1,
    "Adrenocortical_carcinoma|_hereditary|Basal_cell_carcinoma|_susceptibility_to|_7|Glioma_susceptibility_1|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Li-Fraumeni_syndrome_1|Colorectal_cancer|Familial_cancer_of_breast|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Hepatocellular_carcinoma|Bone_marrow_failure_syndrome_5|Li-Fraumeni_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|not_provided|Li-Fraumeni_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "not_provided|Li-Fraumeni_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome|TP53-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_specified": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1": 2,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Adrenocortical_carcinoma|_hereditary|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Hepatocellular_carcinoma|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Glioma_susceptibility_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|not_specified": 1,
    "not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Breast_and/or_ovarian_cancer|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast_carcinoma": 1,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 2,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Ovarian_neoplasm": 1,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Adrenal_cortex_carcinoma|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Familial_melanoma|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Ovarian_neoplasm": 1,
    "Gastric_cancer|TP53-related_disorder|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|B-cell_chronic_lymphocytic_leukemia|Ovarian_neoplasm|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Adrenal_cortex_carcinoma": 1,
    "Adrenocortical_carcinoma|_hereditary|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Glioma_susceptibility_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Li-Fraumeni_syndrome": 3,
    "Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "not_provided|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|not_specified|Li-Fraumeni_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Ovarian_neoplasm": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Bone_osteosarcoma|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Malignant_tumor_of_breast": 2,
    "TP53-related_disorder|Lip_and_oral_cavity_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Poly_(ADP-Ribose)_polymerase_inhibitor_response": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck|Familial_cancer_of_breast": 1,
    "TP53-related_disorder|Mediastinal_germ_cell_tumor|Acute_megakaryoblastic_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|not_provided|Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome": 3,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 3,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 3,
    "Small_cell_carcinoma_of_the_ovary|_hypercalcemic_type": 1,
    "Hereditary_cancer-predisposing_syndrome|Lip_and_oral_cavity_carcinoma|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 2,
    "Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Bone_marrow_failure_syndrome_5|Colorectal_cancer|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|not_provided|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_provided|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome|Lung_adenocarcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Malignant_tumor_of_esophagus": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|not_specified|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenal_cortex_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenal_cortex_carcinoma|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|not_specified|Li-Fraumeni_syndrome_1": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Familial_colorectal_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ovarian_neoplasm|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|not_provided": 1,
    "not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|not_provided": 1,
    "Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Hepatocellular_carcinoma|Bone_osteosarcoma|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Basal_cell_carcinoma|_susceptibility_to|_7|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Li-Fraumeni_syndrome_1|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Prostate_cancer|_hereditary|_1|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Glioma_susceptibility_1": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Adrenocortical_carcinoma|_hereditary|Carcinoma_of_pancreas|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "Li-Fraumeni_syndrome_1|Adrenal_cortex_carcinoma|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Acute_myeloid_leukemia|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Li-Fraumeni_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 2,
    "Prostate_cancer|_hereditary|_1|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|Li-Fraumeni_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Bone_osteosarcoma|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Colorectal_cancer|TP53-related_disorder|Li-Fraumeni_syndrome|Ovarian_neoplasm": 1,
    "TP53-related_disorder|Familial_ovarian_cancer|Adrenal_cortex_carcinoma|Squamous_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Ovarian_neoplasm": 1,
    "Lip_and_oral_cavity_carcinoma|Hepatocellular_carcinoma|Familial_cancer_of_breast|Bone_marrow_failure_syndrome_5|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Adrenocortical_carcinoma|_hereditary|Colorectal_cancer|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Nasopharyngeal_carcinoma|TP53-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_esophagus|Li-Fraumeni_syndrome|Ovarian_neoplasm|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Li-Fraumeni_syndrome_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Lip_and_oral_cavity_carcinoma|TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1": 1,
    "Ovarian_neoplasm|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1": 1,
    "Lip_and_oral_cavity_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Familial_cancer_of_breast": 1,
    "Choroid_plexus_papilloma|Bone_osteosarcoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome": 1,
    "Choroid_plexus_papilloma|Bone_marrow_failure_syndrome_5|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Bone_osteosarcoma|Li-Fraumeni_syndrome_1|Basal_cell_carcinoma|_susceptibility_to|_7|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Colorectal_cancer|TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|Breast_and/or_ovarian_cancer|not_provided|Li-Fraumeni_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Lip_and_oral_cavity_carcinoma": 1,
    "Li-Fraumeni_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Squamous_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hepatocellular_carcinoma|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Bone_osteosarcoma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Carcinoma_of_pancreas|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Li-Fraumeni_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Ovarian_neoplasm|Lung_sarcomatoid_carcinoma": 1,
    "Hepatocellular_carcinoma|Adrenocortical_carcinoma|_hereditary|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Bone_osteosarcoma|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Hereditary_cancer-predisposing_syndrome|Sarcoma|not_specified|not_provided|Malignant_tumor_of_urinary_bladder|Li-Fraumeni_syndrome": 1,
    "Sarcoma|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Ovarian_neoplasm|TP53-related_disorder|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Lip_and_oral_cavity_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Glioma_susceptibility_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Prostate_cancer|_hereditary|_1": 1,
    "Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast_adenocarcinoma": 1,
    "Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast_adenocarcinoma|Adrenocortical_carcinoma|_hereditary": 1,
    "Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Prostate_cancer|_hereditary|_1": 1,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary": 1,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|not_provided|Li-Fraumeni_syndrome": 1,
    "Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary": 1,
    "Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Bone_osteosarcoma|Familial_pancreatic_carcinoma|Colorectal_cancer|Adrenocortical_carcinoma|_hereditary|Nasopharyngeal_carcinoma|Li-Fraumeni_syndrome_1|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Glioma_susceptibility_1|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Hepatocellular_carcinoma|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 2,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome|Prostate_cancer|_hereditary|_1": 1,
    "Adrenocortical_carcinoma|_hereditary|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Familial_pancreatic_carcinoma|Glioma_susceptibility_1|Bone_osteosarcoma|Hepatocellular_carcinoma|Colorectal_cancer|Li-Fraumeni_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 2,
    "Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "Li-Fraumeni_syndrome|Breast_carcinoma": 1,
    "not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome|Glioma_susceptibility_1|Familial_cancer_of_breast|Hepatocellular_carcinoma|Bone_osteosarcoma|Familial_pancreatic_carcinoma|Li-Fraumeni_syndrome_1|Colorectal_cancer|Choroid_plexus_papilloma|Bone_marrow_failure_syndrome_5|Nasopharyngeal_carcinoma|Adrenocortical_carcinoma|_hereditary|Basal_cell_carcinoma|_susceptibility_to|_7|TP53-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary": 1,
    "Ovarian_neoplasm|Prostate_cancer|_hereditary|_1": 1,
    "Bone_osteosarcoma|Adrenocortical_carcinoma|_hereditary|Colorectal_cancer|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Glioma_susceptibility_1|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Prostate_cancer|_hereditary|_1": 1,
    "Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Prostate_cancer|_hereditary|_1|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Li-Fraumeni_syndrome|Prostate_cancer|_hereditary|_1|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_1|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|not_provided": 1,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|TP53-related_disorder": 1,
    "TP53-related_disorder|Li-Fraumeni_syndrome_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Lip_and_oral_cavity_carcinoma|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Gallbladder_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Prostate_cancer|_hereditary|_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Prostate_cancer|_hereditary|_1": 1,
    "not_specified|Li-Fraumeni_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Squamous_cell_carcinoma_of_the_head_and_neck|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|not_specified": 1,
    "Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|Breast_and/or_ovarian_cancer|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Prostate_cancer|Glioma_susceptibility_1": 1,
    "TP53-related_disorder|Li-Fraumeni_syndrome_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|not_provided|Ovarian_neoplasm|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Li-fraumeni-like_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|not_specified": 1,
    "not_provided|TP53-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Acute_myeloid_leukemia|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Adrenal_cortex_carcinoma|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Malignant_tumor_of_breast": 1,
    "TP53-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Ovarian_neoplasm|Li-Fraumeni_syndrome_1": 2,
    "Li-Fraumeni_syndrome|not_provided": 1,
    "Li-Fraumeni_syndrome|Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_pancreatic_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "not_provided|not_specified|Li-Fraumeni_syndrome": 1,
    "Lung_adenocarcinoma|Ovarian_neoplasm|Li-Fraumeni_syndrome": 1,
    "Adrenal_cortex_carcinoma|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary": 1,
    "Malignant_tumor_of_esophagus|not_provided|Ovarian_neoplasm|Adrenocortical_carcinoma|_hereditary|Choroid_plexus_papilloma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Bone_marrow_failure_syndrome_5|Colorectal_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Basal_cell_carcinoma|_susceptibility_to|_7": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Malignant_tumor_of_urinary_bladder|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 2,
    "Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Adrenocortical_carcinoma|_hereditary|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Nasopharyngeal_carcinoma|Choroid_plexus_papilloma|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Bone_marrow_failure_syndrome_5|Basal_cell_carcinoma|_susceptibility_to|_7|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "not_provided|Ovarian_neoplasm": 2,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck|Malignant_tumor_of_breast": 1,
    "Multiple_myeloma|Adrenocortical_carcinoma|_hereditary|Hereditary_cancer-predisposing_syndrome|not_provided|Li-fraumeni-like_syndrome|Breast_and/or_ovarian_cancer|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Nasopharyngeal_carcinoma|Adrenocortical_carcinoma|_hereditary|Bone_marrow_failure_syndrome_5|Hepatocellular_carcinoma|Bone_osteosarcoma|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Glioma_susceptibility_1|Colorectal_cancer|Basal_cell_carcinoma|_susceptibility_to|_7|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Lip_and_oral_cavity_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Acute_myeloid_leukemia|Hereditary_breast_ovarian_cancer_syndrome|TP53_POLYMORPHISM|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome": 1,
    "not_specified|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Ovarian_neoplasm|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Adrenocortical_carcinoma|_hereditary|Li-Fraumeni_syndrome_1|Nasopharyngeal_carcinoma|Colorectal_cancer|Familial_cancer_of_breast|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_osteosarcoma|Hepatocellular_carcinoma|Glioma_susceptibility_1|Bone_marrow_failure_syndrome_5|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Adrenocortical_carcinoma|_hereditary|Choroid_plexus_papilloma|Bone_osteosarcoma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Bone_marrow_failure_syndrome_5|Familial_cancer_of_breast|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Colorectal_cancer|Nasopharyngeal_carcinoma|Basal_cell_carcinoma|_susceptibility_to|_7|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "Li-Fraumeni_syndrome|Carcinoma_of_pancreas": 1,
    "not_provided|Li-Fraumeni_syndrome_1|TP53-related_disorder": 1,
    "Adrenocortical_carcinoma|_hereditary|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Familial_cancer_of_breast|Hepatocellular_carcinoma|Bone_marrow_failure_syndrome_5|Colorectal_cancer|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|TP53-related_disorder|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|not_provided|not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Li-Fraumeni_syndrome_1|Carcinoma_of_colon|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Glioma_susceptibility_1|Bone_osteosarcoma|Nasopharyngeal_carcinoma|Carcinoma_of_pancreas|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7|Hepatocellular_carcinoma|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "not_specified|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome": 1,
    "Colorectal_cancer|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Li-Fraumeni_syndrome|not_provided|Li-Fraumeni_syndrome_1": 1,
    "Li-Fraumeni_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 157,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Endometrial_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Colorectal_cancer|Adrenocortical_carcinoma|_hereditary|Glioma_susceptibility_1|Li-Fraumeni_syndrome_1|Bone_marrow_failure_syndrome_5|Choroid_plexus_papilloma|Basal_cell_carcinoma|_susceptibility_to|_7": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Squamous_cell_carcinoma_of_the_head_and_neck": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 2,
    "TP53-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|not_provided|not_specified|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Adrenocortical_carcinoma|_hereditary|Familial_cancer_of_breast|Choroid_plexus_papilloma|Familial_pancreatic_carcinoma|Hepatocellular_carcinoma|Bone_osteosarcoma|Li-Fraumeni_syndrome_1|Colorectal_cancer|Glioma_susceptibility_1|Nasopharyngeal_carcinoma|Basal_cell_carcinoma|_susceptibility_to|_7|Bone_marrow_failure_syndrome_5|Li-Fraumeni_syndrome": 1,
    "not_specified|Lung_adenocarcinoma|Li-Fraumeni_syndrome": 1,
    "TP53-related_disorder|Familial_cancer_of_breast|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "not_provided|Li-Fraumeni_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|Glioma_susceptibility_1|Bone_osteosarcoma|Adrenocortical_carcinoma|_hereditary|Basal_cell_carcinoma|_susceptibility_to|_7|Hepatocellular_carcinoma|Bone_marrow_failure_syndrome_5|Nasopharyngeal_carcinoma|Colorectal_cancer|Carcinoma_of_pancreas|Choroid_plexus_papilloma|not_specified": 1,
    "Li-Fraumeni_syndrome|Dyskeratosis_Congenita|_Recessive": 1,
    "Li-Fraumeni_syndrome_1|Dyskeratosis_Congenita|_Recessive": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_3": 20,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_3|Li-Fraumeni_syndrome": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_3|Li-Fraumeni_syndrome": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_3|not_provided": 12,
    "Dyskeratosis_Congenita|_Recessive|not_provided|WRAP53-related_disorder|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3|Li-Fraumeni_syndrome": 1,
    "Dyskeratosis_congenita|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3": 2,
    "not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3": 2,
    "not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3|Li-Fraumeni_syndrome|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3|not_provided": 1,
    "not_provided|WRAP53-related_disorder": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_3": 17,
    "Dyskeratosis_congenita|_autosomal_recessive_3|Dyskeratosis_congenita|not_provided": 5,
    "not_specified|Dyskeratosis_Congenita|_Recessive|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3|Li-Fraumeni_syndrome": 1,
    "WRAP53-related_disorder": 3,
    "not_provided|not_specified|Dyskeratosis_congenita|_autosomal_recessive_3|Li-Fraumeni_syndrome|Dyskeratosis_congenita": 1,
    "WRAP53-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "not_provided|WRAP53-related_disorder|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_3|not_specified|Dyskeratosis_congenita|not_provided": 1,
    "WRAP53-related_disorder|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_3|WRAP53-related_disorder|not_provided": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3|Dyskeratosis_congenita": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3|not_specified": 2,
    "WRAP53-related_disorder|not_provided|not_specified|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_3|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "WRAP53-related_disorder|not_provided": 3,
    "WRAP53-related_disorder|Dyskeratosis_congenita|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3|not_provided|not_specified": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_3|not_specified": 1,
    "not_specified|Dyskeratosis_congenita|not_provided": 3,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "not_provided|Dyskeratosis_congenita|not_specified|Dyskeratosis_congenita|_autosomal_recessive_3": 1,
    "DNAH2-related_disorder": 65,
    "DNAH2-related_disorder|not_specified|not_provided": 2,
    "not_provided|DNAH2-related_disorder": 20,
    "not_provided|DNAH2-related_disorder|not_specified": 3,
    "DNAH2-related_disorder|not_provided": 11,
    "not_provided|Spermatogenic_failure_45|DNAH2-related_disorder": 1,
    "not_provided|DNAH2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|DNAH2-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|DNAH2-related_disorder": 1,
    "DNAH2-related_disorder|Spermatogenic_failure_45": 1,
    "not_provided|not_specified|DNAH2-related_disorder": 2,
    "DNAH2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Spermatogenic_failure_45": 1,
    "Spermatogenic_failure_45": 10,
    "not_specified|DNAH2-related_disorder|not_provided": 4,
    "DNAH2-related_disorder|not_provided|not_specified": 1,
    "KDM6B-related_disorder|Inborn_genetic_diseases": 3,
    "KDM6B-related_disorder": 43,
    "not_provided|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities": 9,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities": 12,
    "not_provided|KDM6B-related_disorder": 8,
    "Inborn_genetic_diseases|KDM6B-related_disorder": 6,
    "not_provided|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|Neurodevelopmental_abnormality": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|not_provided": 14,
    "KDM6B-related_disorder|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities": 3,
    "KDM6B-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|not_provided|Intellectual_disability": 1,
    "not_provided|not_specified|KDM6B-related_disorder": 2,
    "Oromandibular-limb_hypogenesis_spectrum|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|not_provided|not_specified": 1,
    "KDM6B-related_disorder|not_provided": 14,
    "not_specified|KDM6B-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|not_provided|not_specified": 1,
    "not_provided|KDM6B-related_disorder|not_specified": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|KDM6B-related_disorder|not_provided": 2,
    "not_provided|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|Neurodevelopmental_delay": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|KDM6B-related_disorder|not_provided": 1,
    "KDM6B-related_neurodevelopmental_disorder": 2,
    "KDM6B-related_disorder|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|not_provided": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|Inborn_genetic_diseases|See_cases": 1,
    "Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities|KDM6B-related_disorder": 1,
    "KDM6B-related_disorder|Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_coarse_facies_and_mild_distal_skeletal_abnormalities": 1,
    "Snijders_Blok-Campeau_syndrome": 130,
    "CHD3-related_disorder": 42,
    "CHD3-related_disorder|Autism_spectrum_disorder": 1,
    "not_provided|Snijders_Blok-Campeau_syndrome": 8,
    "not_provided|CHD3-related_disorder": 10,
    "CHD3-related_disorder|not_provided": 6,
    "Inborn_genetic_diseases|CHD3-related_disorder": 3,
    "not_provided|CHD3-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Snijders_Blok-Campeau_syndrome": 8,
    "CHD3-related_disorder|Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases": 1,
    "CHD3-related_disorder|Inborn_genetic_diseases": 3,
    "Snijders_Blok-Campeau_syndrome|CHD3-related_disorder": 1,
    "Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases": 5,
    "CHD3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_ocular_coloboma|Inborn_genetic_diseases": 1,
    "Snijders_Blok-Campeau_syndrome|Intellectual_disability|Neurodevelopmental_abnormality": 1,
    "Intellectual_disability|Snijders_Blok-Campeau_syndrome": 2,
    "Snijders_Blok-Campeau_syndrome|Intellectual_disability": 10,
    "CHD3-related_disorder|Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Snijders_Blok-Campeau_syndrome|not_provided|Intellectual_disability": 1,
    "Snijders_Blok-Campeau_syndrome|not_provided": 4,
    "Intellectual_disability|Snijders_Blok-Campeau_syndrome|Global_developmental_delay": 1,
    "Snijders_Blok-Campeau_syndrome|Intellectual_disability|Marfanoid_habitus_and_intellectual_disability|not_provided": 1,
    "Intellectual_disability|not_provided|Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases": 1,
    "Intellectual_disability|not_provided|Snijders_Blok-Campeau_syndrome": 1,
    "not_provided|Snijders_Blok-Campeau_syndrome|Inborn_genetic_diseases|Intellectual_disability": 1,
    "Snijders_Blok-Campeau_syndrome|not_specified": 1,
    "CHD3-related_disorder|Snijders_Blok-Campeau_syndrome": 1,
    "not_specified|CHD3-related_disorder": 1,
    "not_provided|CHD3-related_disorder|Inborn_genetic_diseases|Snijders_Blok-Campeau_syndrome": 1,
    "CHD3-related_disorder|not_provided|Snijders_Blok-Campeau_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Snijders_Blok-Campeau_syndrome|CHD3-related_disorder": 1,
    "Snijders_Blok-Campeau_syndrome|CHD3-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Leber_congenital_amaurosis_1": 2,
    "GUCY2D-related_disorder": 7,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 559,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 476,
    "not_provided|GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis_1": 2,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided": 15,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Inborn_genetic_diseases": 15,
    "Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i": 1,
    "GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_specified|not_provided": 2,
    "GUCY2D-related_disorder|Progressive_cone_dystrophy_(without_rod_involvement)|Cone-rod_dystrophy_6|Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|GUCY2D-related_recessive_retinopathy|not_provided": 1,
    "GUCY2D-related_recessive_retinopathy": 7,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|not_provided": 2,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Inborn_genetic_diseases": 9,
    "not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Inborn_genetic_diseases": 4,
    "Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Retinal_dystrophy|not_provided": 1,
    "GUCY2D-related_recessive_retinopathy|Night_blindness|_congenital_stationary|_type1i|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|GUCY2D-related_disorder|Retinal_dystrophy|not_specified|not_provided|Abnormal_electroretinogram|Nystagmus": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 1,
    "Night_blindness|_congenital_stationary|_type1i|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Choroidal_dystrophy|_central_areolar|_1|GUCY2D-related_recessive_retinopathy|not_specified|not_provided": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|not_provided|not_specified": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_disorder": 1,
    "not_provided|Cone_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_specified": 1,
    "Night_blindness|_congenital_stationary|_type1i": 2,
    "GUCY2D-related_recessive_retinopathy|GUCY2D-related_disorder|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided": 2,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided": 13,
    "Retinal_dystrophy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 3,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis|not_provided|Cone_dystrophy|GUCY2D-related_recessive_retinopathy|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 2,
    "GUCY2D-related_recessive_retinopathy|not_specified|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i|GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis": 1,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 30,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 6,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Inborn_genetic_diseases|not_provided": 1,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|GUCY2D-related_disorder": 3,
    "not_specified|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 4,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_specified": 2,
    "Leber_congenital_amaurosis_1|Leber_congenital_amaurosis": 2,
    "not_provided|not_specified|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "GUCY2D-related_recessive_retinopathy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "not_specified|Leber_congenital_amaurosis_1|not_provided": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i": 6,
    "GUCY2D-related_disorder|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 4,
    "not_specified|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 2,
    "GUCY2D-related_recessive_retinopathy|not_provided": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i": 4,
    "Inborn_genetic_diseases|Retinal_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_specified|not_provided": 4,
    "not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Retinal_dystrophy": 2,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided|Inborn_genetic_diseases": 2,
    "GUCY2D-related_disorder|not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 1,
    "Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|Cone-rod_dystrophy_6|not_provided|Leber_congenital_amaurosis": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|not_provided|GUCY2D-related_recessive_retinopathy": 1,
    "Night_blindness|_congenital_stationary|_type1i|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|GUCY2D-related_disorder|Retinal_dystrophy|not_specified|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 7,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided|GUCY2D-related_disorder": 1,
    "Leber_congenital_amaurosis_1|Retinal_disorders": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy": 3,
    "not_provided|Choroidal_dystrophy|_central_areolar|_1|Abnormal_electroretinogram|Nystagmus|GUCY2D-related_recessive_retinopathy|GUCY2D-related_disorder|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "GUCY2D-related_disorder|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 3,
    "Night_blindness|_congenital_stationary|_type1i|Cone-rod_dystrophy_6|Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1": 4,
    "GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Retinal_dystrophy|not_provided": 1,
    "not_specified|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided|GUCY2D-related_recessive_retinopathy|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i": 1,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis|Retinal_dystrophy": 1,
    "not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|GUCY2D-related_disorder|GUCY2D-related_recessive_retinopathy": 1,
    "not_specified|not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 1,
    "GUCY2D-related_recessive_retinopathy|Choroidal_dystrophy|_central_areolar|_1|Retinal_dystrophy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 1,
    "not_provided|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "Choroidal_dystrophy|_central_areolar|_1": 3,
    "Autosomal_recessive_optic_atrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_specified|GUCY2D-related_recessive_retinopathy|not_provided": 2,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Retinal_dystrophy": 1,
    "Night_blindness|_congenital_stationary|_type1i|GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|GUCY2D-related_disorder": 1,
    "Leber_congenital_amaurosis|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i|Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy": 1,
    "Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|not_provided": 2,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Retinal_dystrophy|not_provided": 4,
    "GUCY2D-related_recessive_retinopathy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided|not_specified|GUCY2D-related_recessive_retinopathy|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i": 1,
    "not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 5,
    "Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|Retinal_dystrophy|Cone-rod_dystrophy_6|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i|Leber_congenital_amaurosis": 1,
    "GUCY2D-related_disorder|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided": 1,
    "not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_specified": 1,
    "Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i|GUCY2D-related_recessive_retinopathy": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i|Retinal_dystrophy|Choroidal_dystrophy|_central_areolar|_1": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 3,
    "not_provided|Cone-rod_dystrophy_6|Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|Inborn_genetic_diseases|GUCY2D-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "not_specified|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|not_provided|GUCY2D-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i": 1,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_disorder|not_provided": 1,
    "GUCY2D-related_recessive_retinopathy|Retinal_dystrophy|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i|not_provided": 1,
    "Autosomal_recessive_optic_atrophy": 1,
    "Leber_congenital_amaurosis|Retinal_dystrophy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 1,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Retinal_dystrophy": 3,
    "Night_blindness|_congenital_stationary|_type1i|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Retinal_dystrophy": 1,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Retinal_dystrophy|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i|not_provided": 1,
    "GUCY2D-related_recessive_retinopathy|Night_blindness|_congenital_stationary|_type1i|GUCY2D-related_disorder|Leber_congenital_amaurosis_1|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Retinal_dystrophy|not_provided|Leber_congenital_amaurosis": 1,
    "Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|not_provided|GUCY2D-related_recessive_retinopathy|POLR-related_leukodystrophy|Leber_congenital_amaurosis": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|Choroidal_dystrophy|_central_areolar|_1|Night_blindness|_congenital_stationary|_type1i": 1,
    "Choroidal_dystrophy|_central_areolar|_1|not_specified|not_provided|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|GUCY2D-related_recessive_retinopathy|Night_blindness|_congenital_stationary|_type1i": 1,
    "Night_blindness|_congenital_stationary|_type1i|Cone-rod_dystrophy_6|Choroidal_dystrophy|_central_areolar|_1|Leber_congenital_amaurosis_1|Retinal_disorders|GUCY2D-related_recessive_retinopathy|not_provided|Retinal_dystrophy": 1,
    "Optic_atrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Cataract|Retinal_dystrophy": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Retinal_dystrophy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided|Cone_dystrophy": 1,
    "Retinal_disorders|Progressive_cone_dystrophy_(without_rod_involvement)|Retinal_dystrophy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy|Cone_dystrophy|Visual_impairment|Macular_dystrophy": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Retinal_dystrophy|not_specified": 1,
    "GUCY2D_retinopathy|Leber_congenital_amaurosis_1": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Cone-rod_dystrophy": 1,
    "Night_blindness|_congenital_stationary|_type1i|Choroidal_dystrophy|_central_areolar|_1|not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_specified|not_provided|GUCY2D-related_recessive_retinopathy": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|Night_blindness|_congenital_stationary|_type1i|Choroidal_dystrophy|_central_areolar|_1|GUCY2D-related_disorder": 1,
    "Cone-rod_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Night_blindness|_congenital_stationary|_type1i|Retinal_dystrophy": 1,
    "not_specified|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|not_provided": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|Leber_congenital_amaurosis": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy": 1,
    "Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6|Leber_congenital_amaurosis|not_provided|Retinal_dystrophy": 1,
    "GUCY2D-related_recessive_retinopathy|Choroidal_dystrophy|_central_areolar|_1|not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1": 1,
    "Optic_atrophy|Retinal_dystrophy|not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|GUCY2D-related_disorder": 1,
    "Congenital_blindness": 1,
    "Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_provided|GUCY2D-related_recessive_retinopathy": 1,
    "not_specified|not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy": 1,
    "GUCY2D-related_recessive_retinopathy|Leber_congenital_amaurosis_1": 1,
    "Leber_congenital_amaurosis_1|not_provided|Cone-rod_dystrophy_6": 1,
    "Night_blindness|_congenital_stationary|_type1i|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 1,
    "Inborn_genetic_diseases|GUCY2D-related_disorder": 1,
    "Early-onset_retinal_dystrophy": 1,
    "Choroidal_dystrophy|_central_areolar|_1|Cone-rod_dystrophy_6|Night_blindness|_congenital_stationary|_type1i|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy|Retinal_dystrophy": 1,
    "not_provided|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|not_specified": 2,
    "Early-onset_retinal_dystrophy|Leber_congenital_amaurosis_1": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Leber_congenital_amaurosis_1|Cone-rod_dystrophy_6": 2,
    "Retinal_dystrophy|Cone-rod_dystrophy_6|Leber_congenital_amaurosis_1|GUCY2D-related_recessive_retinopathy": 1,
    "Autosomal_recessive_congenital_ichthyosis_3": 77,
    "Autosomal_recessive_congenital_ichthyosis_2": 145,
    "Autosomal_recessive_congenital_ichthyosis_2|not_provided": 21,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_2|Lamellar_ichthyosis": 2,
    "Ichthyosis|Autosomal_recessive_congenital_ichthyosis_2|not_specified": 1,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_2": 4,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_2": 19,
    "Lamellar_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_2|Congenital_nonbullous_ichthyosiform_erythroderma|Congenital_ichthyosiform_erythroderma": 1,
    "Autosomal_recessive_congenital_ichthyosis_2|not_specified": 3,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_2": 5,
    "Lamellar_ichthyosis|not_provided|Ichthyosis|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "ALOX12B-related_disorder|not_provided": 3,
    "Autosomal_recessive_congenital_ichthyosis_2|ALOX12B-related_disorder|Lamellar_ichthyosis": 1,
    "Autosomal_recessive_congenital_ichthyosis|Autosomal_recessive_congenital_ichthyosis_2|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_2|ALOX12B-related_disorder|not_provided": 2,
    "ALOX12B-related_disorder": 2,
    "not_provided|ALOX12B-related_disorder": 1,
    "Leukoencephalopathy_with_calcifications_and_cysts": 23,
    "Autosomal_recessive_congenital_ichthyosis_2|Lamellar_ichthyosis": 2,
    "See_cases|Autosomal_recessive_congenital_ichthyosis_2|Lamellar_ichthyosis": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_2|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "Autosomal_recessive_congenital_ichthyosis_2|not_specified|not_provided": 2,
    "Autosomal_recessive_congenital_ichthyosis_2|ALOX12B-related_disorder": 1,
    "Autosomal_recessive_congenital_ichthyosis_2|not_provided|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "Autosomal_recessive_congenital_ichthyosis_2|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_congenital_ichthyosis_2|Inborn_genetic_diseases|ALOX12B-related_disorder|not_provided": 1,
    "ALOX12B-related_disorder|not_provided|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|not_provided": 21,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_3": 12,
    "ALOXE3-related_disorder": 4,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_3": 3,
    "ALOXE3-related_disorder|not_provided": 2,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "ALOXE3-related_disorder|Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis|not_provided|Autosomal_recessive_congenital_ichthyosis_3": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|not_provided|Inborn_genetic_diseases": 1,
    "ALOXE3-related_disorder|Congenital_ichthyosiform_erythroderma": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|ALOXE3-related_disorder": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "Lamellar_ichthyosis|Congenital_nonbullous_ichthyosiform_erythroderma|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|Autosomal_recessive_congenital_ichthyosis_2|Lamellar_ichthyosis": 1,
    "not_specified|Autosomal_recessive_congenital_ichthyosis_3": 1,
    "not_provided|ALOXE3-related_disorder": 2,
    "Autosomal_recessive_congenital_ichthyosis_3|not_specified": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|Inborn_genetic_diseases": 3,
    "Autosomal_recessive_congenital_ichthyosis_3|not_provided|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_3": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_3": 1,
    "ALOXE3-related_disorder|Autosomal_recessive_congenital_ichthyosis_2|Autosomal_recessive_congenital_ichthyosis_3|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|Lamellar_ichthyosis|Trichohepatoenteric_syndrome_2": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_3|ALOXE3-related_disorder": 1,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_3|Ichthyosis": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|not_specified|Autosomal_recessive_congenital_ichthyosis_2": 1,
    "Congenital_elevation_of_scapula|Mitral_regurgitation|Progressive_microcephaly|Delayed_ability_to_walk|Delayed_ability_to_stand|Mild_malformation_of_cortical_development|Brachycephaly|Short_stature|Scoliosis|Hemivertebrae|Tapered_finger|Failure_to_thrive_in_infancy|Short_neck|Mild_global_developmental_delay|Skeletal_dysplasia|Thoracic_kyphoscoliosis|Hypophosphatemia|Intellectual_disability|Neuropathic_spinal_arthropathy|Progressive_congenital_scoliosis|Childhood-onset_short-trunk_short_stature|Delayed_fine_motor_development|Thoracic_scoliosis|Vertebral_fusion|Abnormal_form_of_the_vertebral_bodies|Thoracolumbar_kyphoscoliosis|Disproportionate_short_stature|Decreased_body_weight|Lumbar_kyphoscoliosis|Severe_failure_to_thrive": 1,
    "Autosomal_recessive_congenital_ichthyosis_3|ALOXE3-related_disorder|not_provided": 1,
    "HES7-related_disorder|not_provided": 2,
    "Spondylocostal_dysostosis_4|_autosomal_recessive": 4,
    "not_provided|HES7-related_disorder": 1,
    "not_provided|Spondylocostal_dysostosis_4|_autosomal_recessive": 2,
    "not_provided|Inborn_genetic_diseases|HES7-related_disorder": 1,
    "Spondylocostal_dysostosis_4|_autosomal_recessive|Spondylocostal_dysostosis_2|_autosomal_recessive": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_autistic_features_with_or_without_hyperkinetic_movements|not_provided": 1,
    "Neurodevelopmental_disorder_with_hypotonia_and_autistic_features_with_or_without_hyperkinetic_movements": 7,
    "Neurodevelopmental_disorder_with_hypotonia_and_autistic_features_with_or_without_hyperkinetic_movements|Inborn_genetic_diseases": 1,
    "VAMP2-related_disorder": 3,
    "Neurodevelopmental_disorder_with_hypotonia_and_autistic_features_with_or_without_hyperkinetic_movements|Severe_neurodevelopmental_delay": 1,
    "Inborn_genetic_diseases|VAMP2-related_disorder": 1,
    "VAMP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|TMEM107-related_disorder": 7,
    "TMEM107-related_disorder": 14,
    "Leukoencephalopathy_with_calcifications_and_cysts|not_specified|TMEM107-related_disorder|not_provided|Meckel-Gruber_syndrome": 1,
    "not_provided|Meckel-Gruber_syndrome|Orofaciodigital_syndrome_16|Leukoencephalopathy_with_calcifications_and_cysts": 1,
    "TMEM107-related_disorder|Meckel_syndrome|_type_1|Leukoencephalopathy_with_calcifications_and_cysts": 1,
    "Leukoencephalopathy_with_calcifications_and_cysts|not_provided": 14,
    "not_specified|Meckel_syndrome_13|TMEM107-related_disorder|Leukoencephalopathy_with_calcifications_and_cysts|not_provided": 1,
    "TMEM107-related_disorder|not_provided": 8,
    "not_provided|Leukoencephalopathy_with_calcifications_and_cysts": 4,
    "not_provided|Meckel_syndrome_13|Leukoencephalopathy_with_calcifications_and_cysts": 1,
    "Leukoencephalopathy_with_calcifications_and_cysts|not_specified": 1,
    "Meckel-Gruber_syndrome|not_provided|Leukoencephalopathy_with_calcifications_and_cysts": 1,
    "Leukoencephalopathy_with_calcifications_and_cysts|Meckel_syndrome_13|not_provided": 2,
    "not_specified|not_provided|Leukoencephalopathy_with_calcifications_and_cysts": 1,
    "Leukoencephalopathy_with_calcifications_and_cysts|Meckel_syndrome_13|not_specified|not_provided": 1,
    "Meckel_syndrome_13": 3,
    "Orofaciodigital_syndrome|Orofaciodigital_syndrome_16|Joubert_syndrome_29": 1,
    "not_provided|Meckel_syndrome_13|Orofaciodigital_syndrome_16": 2,
    "Orofaciodigital_syndrome_16": 1,
    "not_provided|Orofaciodigital_syndrome_16|Leukoencephalopathy_with_calcifications_and_cysts": 1,
    "AURKB-related_disorder": 1,
    "Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 38,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 6,
    "Inborn_genetic_diseases|Dyskeratosis_congenita": 40,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|Dyskeratosis_congenita|not_specified": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|not_specified": 1,
    "Dyskeratosis_congenita|CTC1-related_disorder": 6,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 28,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 32,
    "Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided": 11,
    "CTC1-related_disorder|Dyskeratosis_congenita": 9,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|Dyskeratosis_congenita": 6,
    "not_provided|not_specified|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases": 38,
    "CTC1-related_disorder": 6,
    "not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita|not_specified": 1,
    "Dyskeratosis_congenita|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 7,
    "not_provided|Inborn_genetic_diseases|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|CTC1-related_disorder|Dyskeratosis_congenita|not_specified": 1,
    "Inborn_genetic_diseases|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 3,
    "Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita": 1,
    "not_provided|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 10,
    "not_specified|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita": 1,
    "not_provided|CTC1-related_disorder|Dyskeratosis_congenita|Coats_plus_syndrome|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 5,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|Dyskeratosis_congenita|CTC1-related_disorder": 1,
    "Dyskeratosis_congenita|Coats_plus_syndrome|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases": 2,
    "CTC1-related_disorder|Coats_plus_syndrome|not_provided|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|not_provided": 5,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|Inborn_genetic_diseases": 4,
    "not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "CTC1-related_disorder|not_specified|not_provided|Dyskeratosis_congenita|Inborn_genetic_diseases": 1,
    "not_provided|Dyskeratosis_congenita|CTC1-related_disorder|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_specified": 1,
    "Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|not_provided": 1,
    "Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|not_specified": 1,
    "not_specified|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided": 2,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|not_provided": 5,
    "Inborn_genetic_diseases|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|not_provided": 2,
    "Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita": 1,
    "CTC1-related_disorder|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|Dyskeratosis_congenita|not_specified": 1,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|not_specified": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 4,
    "CTC1-related_disorder|Dyskeratosis_congenita|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 2,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|not_specified": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|not_specified": 3,
    "CTC1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|Dyskeratosis_congenita|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|CTC1-related_disorder|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|CTC1-related_disorder|not_specified|Dyskeratosis_congenita": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|Dyskeratosis_congenita": 2,
    "CTC1-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "CTC1-related_disorder|not_specified|Dyskeratosis_congenita": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_specified|Dyskeratosis_congenita|Inborn_genetic_diseases": 1,
    "not_provided|Dyskeratosis_congenita|CTC1-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 2,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases": 1,
    "not_provided|Dyskeratosis_congenita|not_specified|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Dyskeratosis_congenita|CTC1-related_disorder|not_provided": 1,
    "not_specified|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|not_provided": 1,
    "Coats_plus_syndrome|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "CTC1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|CTC1-related_disorder": 1,
    "not_provided|Dyskeratosis_congenita|not_specified": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_specified|Dyskeratosis_congenita|not_provided": 1,
    "CTC1-related_disorder|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "not_specified|Dyskeratosis_congenita|CTC1-related_disorder|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Dyskeratosis_congenita|not_provided|CTC1-related_disorder": 1,
    "CTC1-related_disorder|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 1,
    "CTC1-related_disorder|not_specified|Dyskeratosis_congenita|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|not_specified|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|not_specified|Inborn_genetic_diseases": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Inborn_genetic_diseases|Dyskeratosis_congenita|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|CTC1-related_disorder|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_specified": 1,
    "not_specified|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|Dyskeratosis_congenita": 1,
    "not_specified|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 1,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|CTC1-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "CTC1-related_disorder|not_specified|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|not_provided|Dyskeratosis_congenita": 1,
    "not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Inborn_genetic_diseases|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1": 1,
    "Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Cerebroretinal_microangiopathy_with_calcifications_and_cysts_1|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|not_specified|CTC1-related_disorder": 1,
    "Dyskeratosis_Congenita|_Recessive|not_specified|not_provided": 1,
    "Phosphoribosylformylglycineamidine_synthase_deficiency": 3,
    "Cardiac_arrhythmia|RANGRF-related_disorder": 2,
    "RANGRF-related_disorder|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "ARHGEF15-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|ARHGEF15-related_disorder": 2,
    "ARHGEF15-related_disorder|Developmental_and_epileptic_encephalopathy": 6,
    "Developmental_and_epileptic_encephalopathy|ARHGEF15-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|ARHGEF15-related_disorder": 2,
    "not_provided|ARHGEF15-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "ARHGEF15-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_specified|ARHGEF15-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Prostate_cancer|Developmental_and_epileptic_encephalopathy": 1,
    "not_specified|Diamond-Blackfan_anemia_11|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_11|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia_11": 8,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_11": 4,
    "RPL26-related_disorder|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia|not_specified|RPL26-related_disorder": 1,
    "Diamond-Blackfan_anemia|RPL26-related_disorder": 1,
    "not_specified|Diamond-Blackfan_anemia_11": 1,
    "MYH10-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Jaw-winking_syndrome": 1,
    "MYH10-related_disorder": 24,
    "Inborn_genetic_diseases|Neurodevelopmental_abnormality|not_provided": 1,
    "not_provided|MYH10-related_disorder": 2,
    "MYH10-related_neurodevelopmental_disorder_with_congenital_anomalies": 1,
    "MYH10-related_neurodevelopmental_disorder": 1,
    "Complex_neurodevelopmental_disorder_with_or_without_congenital_anomalies": 1,
    "Hypertelorism|Midface_retrusion|Congenital_ptosis|Epicanthus_inversus|Abnormal_facial_shape|Wide_nose|Congenital_ocular_coloboma": 1,
    "Complex_neurodevelopmental_disorders": 1,
    "Congenital_fibrosis_of_extraocular_muscles|Inborn_genetic_diseases": 2,
    "not_specified|Ataxia_with_oculomotor_apraxia_type_3|not_provided": 1,
    "Ataxia_with_oculomotor_apraxia_type_3": 7,
    "not_provided|Ataxia_with_oculomotor_apraxia_type_3": 4,
    "not_provided|PIK3R5-related_disorder": 1,
    "not_provided|Ataxia_with_oculomotor_apraxia_type_3|not_specified": 2,
    "Ataxia_with_oculomotor_apraxia_type_3|not_provided|not_specified": 3,
    "PIK3R5-related_disorder|not_specified": 1,
    "Ataxia_with_oculomotor_apraxia_type_3|not_specified": 2,
    "PIK3R5-related_disorder|not_provided": 2,
    "not_specified|Spastic_ataxia": 1,
    "not_specified|PIK3R5-related_disorder|not_provided": 1,
    "Ataxia_with_oculomotor_apraxia_type_3|not_specified|not_provided": 2,
    "PIK3R5-related_disorder": 3,
    "NTN1-related_disorder": 22,
    "not_provided|NTN1-related_disorder": 2,
    "Mirror_movements_1|Mirror_movements_4": 2,
    "Nonsyndromic_cleft_lip_with_or_without_cleft_palate|not_provided": 1,
    "Mirror_movements_4": 4,
    "CFAP52-related_disorder": 3,
    "Heterotaxy|_visceral|_10|_autosomal|_with_male_infertility": 2,
    "not_specified|Situs_inversus": 6,
    "Situs_inversus|not_provided": 8,
    "CFAP52-related_disorder|not_provided": 1,
    "Situs_inversus|not_specified": 6,
    "CFAP52-related_disorder|Situs_inversus|not_specified": 1,
    "not_provided|Situs_inversus": 8,
    "not_provided|Heterotaxy|_visceral|_10|_autosomal|_with_male_infertility": 1,
    "Oculomotor_apraxia|Situs_inversus|Heterotaxy|_visceral|_10|_autosomal|_with_male_infertility": 1,
    "MYH13-related_disorder": 6,
    "MYH13-related_disorder|not_specified": 2,
    "not_provided|Hecht_syndrome": 15,
    "Hecht_syndrome": 55,
    "not_specified|not_provided|Hecht_syndrome": 15,
    "not_specified|not_provided|Hecht_syndrome|MYH8-related_disorder": 1,
    "MYH8-related_disorder|not_provided": 2,
    "not_provided|Hecht_syndrome|MYH8-related_disorder": 3,
    "Hecht_syndrome|not_provided": 4,
    "Hecht_syndrome|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hecht_syndrome": 1,
    "not_specified|Hecht_syndrome|not_provided": 2,
    "Neuromuscular_disease|Hecht_syndrome": 1,
    "not_specified|Hecht_syndrome": 5,
    "MYH8-related_disorder": 10,
    "not_provided|MYH8-related_disorder|Hecht_syndrome": 2,
    "not_provided|MYH8-related_disorder|not_specified": 1,
    "Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome": 2,
    "Hecht_syndrome|Hereditary_skeletal_muscle_disorder|not_specified": 1,
    "not_provided|MYH8-related_disorder|not_specified|Hecht_syndrome": 1,
    "Hecht_syndrome|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|not_specified": 1,
    "not_provided|Hecht_syndrome|not_specified|MYH8-related_disorder": 1,
    "not_provided|Hecht_syndrome|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome": 1,
    "not_specified|MYH8-related_disorder|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|Hecht_syndrome|not_provided": 1,
    "Hecht_syndrome|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|MYH8-related_disorder|not_specified": 1,
    "Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|not_provided": 1,
    "not_provided|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|Hecht_syndrome": 1,
    "MYH8-related_disorder|Hecht_syndrome|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|not_provided": 1,
    "Hecht_syndrome|not_specified": 5,
    "Arthrogryposis|_distal|_type_1A|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|Hecht_syndrome": 1,
    "Hecht_syndrome|Carney_complex_-_trismus_-_pseudocamptodactyly_syndrome|not_provided": 1,
    "not_provided|not_specified|MYH8-related_disorder": 1,
    "MYH8-related_disorder|Hecht_syndrome": 1,
    "Hecht_syndrome|not_specified|not_provided": 1,
    "MYH8-related_disorder|not_provided|Hecht_syndrome": 1,
    "not_provided|MYH1-related_disorder": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia": 1015,
    "not_provided|Myopathy|_proximal|_and_ophthalmoplegia": 49,
    "MYH2-related_disorder": 12,
    "MYH2-related_disorder|not_specified|not_provided|Myopathy|_proximal|_and_ophthalmoplegia": 4,
    "Myopathy|_proximal|_and_ophthalmoplegia|Inborn_genetic_diseases": 42,
    "Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia|not_provided": 4,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_provided": 43,
    "MYH2-related_disorder|Myopathy|_proximal|_and_ophthalmoplegia": 5,
    "MYH2-related_disorder|not_provided|Myopathy|_proximal|_and_ophthalmoplegia": 2,
    "Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia": 42,
    "Inborn_genetic_diseases|not_provided|Myopathy|_proximal|_and_ophthalmoplegia": 9,
    "Myopathy|_proximal|_and_ophthalmoplegia|MYH2-related_disorder": 10,
    "Myopathy|_proximal|_and_ophthalmoplegia|Inborn_genetic_diseases|not_provided": 8,
    "not_provided|Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia": 3,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_specified": 4,
    "Myopathy|_proximal|_and_ophthalmoplegia|Inclusion_Body_Myopathy|_Dominant": 20,
    "not_provided|Inborn_genetic_diseases|MYH2-related_disorder|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "MYH2-related_disorder|Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "not_specified|not_provided|Myopathy|_proximal|_and_ophthalmoplegia": 6,
    "not_provided|not_specified|Myopathy|_proximal|_and_ophthalmoplegia": 2,
    "not_specified|Myopathy|_proximal|_and_ophthalmoplegia|not_provided": 4,
    "not_specified|Myopathy|_proximal|_and_ophthalmoplegia": 4,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_specified|not_provided": 2,
    "not_provided|Myopathy|_proximal|_and_ophthalmoplegia|not_specified": 3,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_provided|MYH2-related_disorder": 2,
    "Inclusion_Body_Myopathy|_Dominant|Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia|not_provided": 1,
    "not_provided|Myopathy|_proximal|_and_ophthalmoplegia|Inclusion_Body_Myopathy|_Dominant|not_specified": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_specified|not_provided|MYH2-related_disorder": 1,
    "not_provided|Myopathy|_proximal|_and_ophthalmoplegia|Inborn_genetic_diseases": 4,
    "not_provided|Inborn_genetic_diseases|Inclusion_Body_Myopathy|_Dominant|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Inclusion_Body_Myopathy|_Dominant|Myopathy|_proximal|_and_ophthalmoplegia|Inborn_genetic_diseases|not_provided": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|MYH2-related_disorder|Myopathy|_proximal|_and_ophthalmoplegia": 3,
    "MYH2-related_disorder|not_provided|not_specified|Myopathy|_proximal|_and_ophthalmoplegia": 2,
    "not_specified|Myopathy|_proximal|_and_ophthalmoplegia|Inclusion_Body_Myopathy|_Dominant|Inborn_genetic_diseases": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|not_provided|not_specified": 1,
    "MYH2-related_disorder|Myopathy|_proximal|_and_ophthalmoplegia|not_provided": 1,
    "Inclusion_Body_Myopathy|_Dominant|Myopathy|_proximal|_and_ophthalmoplegia|not_provided": 1,
    "Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia|not_provided|Inclusion_Body_Myopathy|_Dominant": 1,
    "MYH2-related_myopathy|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Inborn_genetic_diseases|not_specified|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Inclusion_Body_Myopathy|_Dominant|Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "MYH2-related_disorder|not_specified|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Hereditary_inclusion_body_myopathy-joint_contractures-ophthalmoplegia_syndrome|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Limb-girdle_muscular_dystrophy|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "MYH2-related_disorder|Myopathy|_proximal|_and_ophthalmoplegia|not_provided|not_specified": 1,
    "not_provided|Myopathy|_proximal|_and_ophthalmoplegia|MYH2-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Inclusion_Body_Myopathy|_Dominant|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Inborn_genetic_diseases|Myopathy|_proximal|_and_ophthalmoplegia|not_specified|not_provided": 1,
    "Inclusion_Body_Myopathy|_Dominant|Myopathy|_proximal|_and_ophthalmoplegia|not_provided|MYH2-related_disorder": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|Childhood-onset_autosomal_recessive_myopathy_with_external_ophthalmoplegia": 1,
    "Hereditary_spherocytosis_type_2|Myopathy|_proximal|_and_ophthalmoplegia": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|MYH2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Myopathy|_proximal|_and_ophthalmoplegia|Inclusion_Body_Myopathy|_Dominant": 1,
    "Myopathy|_proximal|_and_ophthalmoplegia|Inclusion_Body_Myopathy|_Dominant|not_provided": 1,
    "not_provided|Myopathy|_proximal|_and_ophthalmoplegia|Inclusion_Body_Myopathy|_Dominant": 1,
    "not_provided|Inclusion_Body_Myopathy|_Dominant": 1,
    "Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 21,
    "MYH3-related_disorder": 37,
    "Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|not_provided": 8,
    "Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|not_provided|not_specified": 2,
    "not_provided|MYH3-related_disorder": 18,
    "not_provided|Freeman-Sheldon_syndrome|Inborn_genetic_diseases|Distal_arthrogryposis_type_2B1": 2,
    "not_provided|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 26,
    "Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 11,
    "not_provided|Arthrogryposis_multiplex_congenita": 1,
    "Arthrogryposis|_distal|_type_2B3": 12,
    "Arthrogryposis_multiplex_congenita|Freeman-Sheldon_syndrome": 1,
    "Arthrogryposis_multiplex_congenita|not_specified|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|not_provided": 1,
    "Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome|not_provided|not_specified": 1,
    "Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B": 7,
    "MYH3-related_disorder|not_provided": 21,
    "not_provided|Freeman-Sheldon_syndrome|MYH3-related_disorder|Inborn_genetic_diseases|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3": 1,
    "MYH3-related_disorder|not_provided|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 2,
    "not_specified|not_provided|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 2,
    "Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|not_specified|not_provided": 2,
    "not_provided|Distal_arthrogryposis_type_2B1|MYH3-related_disorder|Inborn_genetic_diseases|Freeman-Sheldon_syndrome": 1,
    "Distal_arthrogryposis_type_2B1|not_provided|Freeman-Sheldon_syndrome": 8,
    "not_provided|not_specified|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "Freeman-Sheldon_syndrome|not_provided": 2,
    "not_specified|not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 2,
    "Arthrogryposis_multiplex_congenita|not_provided|not_specified|Freeman-Sheldon_syndrome|Inborn_genetic_diseases": 1,
    "MYH3-related_disorder|not_specified|not_provided|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Freeman-Sheldon_syndrome|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|MYH3-related_disorder": 1,
    "Freeman-Sheldon_syndrome": 10,
    "Freeman-Sheldon_syndrome|not_provided|Distal_arthrogryposis_type_2B1": 6,
    "not_specified|not_provided|Arthrogryposis|_distal|_type_2B3|Distal_arthrogryposis_type_2B1|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome": 1,
    "Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Spondylocarpotarsal_synostosis_syndrome": 2,
    "Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 10,
    "Distal_arthrogryposis_type_2B1|not_provided|MYH3-related_disorder|Freeman-Sheldon_syndrome": 2,
    "not_provided|not_specified|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 3,
    "Inborn_genetic_diseases|not_provided|MYH3-related_disorder": 1,
    "not_specified|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome|not_provided": 4,
    "not_provided|Arthrogryposis|_distal|_type_1A|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Distal_arthrogryposis_type_2B1": 1,
    "Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "not_provided|Freeman-Sheldon_syndrome|MYH3-related_disorder|Distal_arthrogryposis_type_2B1": 5,
    "Distal_arthrogryposis_type_2B1|not_provided|Freeman-Sheldon_syndrome|not_specified": 2,
    "not_provided|Distal_arthrogryposis|Inborn_genetic_diseases": 1,
    "Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3": 2,
    "Inborn_genetic_diseases|Distal_arthrogryposis_type_2B1|not_provided|Freeman-Sheldon_syndrome": 1,
    "Freeman-Sheldon_syndrome|not_specified|not_provided|Distal_arthrogryposis_type_2B1": 2,
    "not_specified|not_provided|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 5,
    "Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|Inborn_genetic_diseases|not_provided": 1,
    "Freeman-Sheldon_syndrome|MYH3-related_disorder|not_provided|Distal_arthrogryposis_type_2B1": 2,
    "not_specified|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|not_provided|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 1,
    "not_provided|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|Inborn_genetic_diseases": 4,
    "not_provided|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B": 1,
    "Freeman-Sheldon_syndrome|MYH3-related_disorder|Arthrogryposis|_distal|_type_2B3|not_provided|Distal_arthrogryposis_type_2B1": 1,
    "Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|not_provided": 1,
    "not_provided|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|MYH3-related_disorder": 4,
    "Distal_arthrogryposis|not_provided": 2,
    "Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|MYH3-related_disorder|not_provided": 1,
    "not_specified|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Distal_arthrogryposis_type_2B1|not_provided": 1,
    "not_provided|not_specified|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 1,
    "Freeman-Sheldon_syndrome|Arthrogryposis|_distal|_type_2B3": 1,
    "Meniere_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|not_provided": 1,
    "Arthrogryposis|_distal|_type_2B3|not_specified|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|not_provided|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Distal_arthrogryposis_type_2B1|not_specified": 2,
    "not_specified|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3|Distal_arthrogryposis_type_2B1|not_provided|Freeman-Sheldon_syndrome": 1,
    "Arthrogryposis|_distal|_type_2B3|Freeman-Sheldon_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|MYH3-related_disorder": 1,
    "Freeman-Sheldon_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|not_provided|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3": 1,
    "Freeman-Sheldon_syndrome|not_provided|MYH3-related_disorder": 1,
    "Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|not_provided|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome|not_specified": 1,
    "Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Arthrogryposis|_distal|_type_2B3": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B3": 2,
    "not_provided|Inborn_genetic_diseases|Freeman-Sheldon_syndrome": 1,
    "not_provided|Distal_arthrogryposis_type_2B1|not_specified|Freeman-Sheldon_syndrome": 1,
    "Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|not_provided": 2,
    "not_provided|Freeman-Sheldon_syndrome|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Distal_arthrogryposis_type_2B1|not_specified": 1,
    "not_specified|not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 1,
    "Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Freeman-Sheldon_syndrome|not_provided": 1,
    "not_provided|Freeman-Sheldon_syndrome": 2,
    "Spondylocarpotarsal_synostosis_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|not_provided": 1,
    "Arthrogryposis_multiplex_congenita|not_specified|Freeman-Sheldon_syndrome|not_provided": 1,
    "Arthrogryposis_multiplex_congenita|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|not_specified|Freeman-Sheldon_syndrome|not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B": 1,
    "not_provided|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 2,
    "Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "Spondylocarpotarsal_fusion_syndrome_1A": 1,
    "Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Spondylocarpotarsal_synostosis_syndrome": 1,
    "not_provided|Freeman-Sheldon_syndrome|not_specified|Distal_arthrogryposis_type_2B1|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "MYH3-related_disorder|Freeman-Sheldon_syndrome|not_provided|Distal_arthrogryposis_type_2B1": 1,
    "Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Spondylocarpotarsal_synostosis_syndrome": 1,
    "Freeman-Sheldon_syndrome|not_specified|Inborn_genetic_diseases|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|not_specified|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "Arthrogryposis|_distal|_type_2B3|MYH3-related_disorder|not_provided": 1,
    "not_specified|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|not_provided|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 2,
    "not_provided|not_specified|Meniere_disease|Distal_arthrogryposis_type_2B1|Rhabdomyolysis|Arthrogryposis|_distal|_type_2B3|Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|MYH3-related_disorder": 1,
    "not_specified|not_provided|MYH3-related_disorder|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A": 1,
    "not_provided|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Spondylocarpotarsal_synostosis_syndrome": 1,
    "Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Freeman-Sheldon_syndrome": 1,
    "not_provided|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|not_specified|Distal_arthrogryposis_type_2B1|Freeman-Sheldon_syndrome": 1,
    "not_provided|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Freeman-Sheldon_syndrome|Arthrogryposis|_distal|_type_2B3|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B": 1,
    "Distal_arthrogryposis_type_2B1|not_specified|not_provided|Freeman-Sheldon_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 1,
    "not_provided|Freeman-Sheldon_syndrome|Arthrogryposis|_distal|_type_2B3|MYH3-related_disorder": 1,
    "Meniere_disease|not_provided|Freeman-Sheldon_syndrome|Inborn_genetic_diseases|Distal_arthrogryposis_type_2B1": 1,
    "not_specified|Freeman-Sheldon_syndrome|MYH3-related_disorder|not_provided|Distal_arthrogryposis_type_2B1": 1,
    "MYH3-related_disorder|not_provided|Meniere_disease|Freeman-Sheldon_syndrome|Distal_arthrogryposis_type_2B1": 1,
    "Freeman-Sheldon_syndrome|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Arthrogryposis|_distal|_type_2B3|Prostate_cancer|not_provided": 1,
    "Contractures|_pterygia|_and_spondylocarpotarsal_fusion_syndrome_1A|Spondylocarpotarsal_synostosis_syndrome|not_provided|Contractures|_pterygia|_and_variable_skeletal_fusions_syndrome_1B|MYH3-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 27,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4": 39,
    "Inborn_genetic_diseases|not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Infantile_encephalopathy": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|SCO1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|SCO1-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided": 3,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_4": 10,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided": 1,
    "SCO1-related_disorder": 3,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided": 5,
    "not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 5,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|SCO1-related_disorder|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Inborn_genetic_diseases|not_provided": 1,
    "Leigh_syndrome|SCO1-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_4": 5,
    "Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_4": 1,
    "not_specified|Leigh_syndrome|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided": 1,
    "not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "SCO1-related_disorder|Leigh_syndrome|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Inborn_genetic_diseases|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "SCO1-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_4|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Inborn_genetic_diseases": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 8,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_4": 1,
    "Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Infantile_encephalopathy|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_4": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_4|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "DNAH9-related_disorder": 32,
    "Ciliary_dyskinesia|_primary|_40|Inborn_genetic_diseases|not_provided": 5,
    "DNAH9-related_disorder|not_provided": 49,
    "not_provided|DNAH9-related_disorder|Inborn_genetic_diseases": 3,
    "Ciliary_dyskinesia|_primary|_40|not_provided": 18,
    "not_provided|DNAH9-related_disorder": 60,
    "Inborn_genetic_diseases|DNAH9-related_disorder|not_provided|Ciliary_dyskinesia|_primary|_40": 2,
    "not_provided|Abnormal_cardiovascular_system_morphology|Hydrocephalus|Ciliary_dyskinesia|_primary|_40|DNAH9-related_disorder": 1,
    "DNAH9-related_disorder|Ciliary_dyskinesia|_primary|_40|not_provided|Primary_ciliary_dyskinesia": 1,
    "DNAH9-related_disorder|Ciliary_dyskinesia|_primary|_40|not_provided": 8,
    "DNAH9-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "Ciliary_dyskinesia|_primary|_40|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|DNAH9-related_disorder": 3,
    "Inborn_genetic_diseases|DNAH9-related_disorder|not_provided": 2,
    "not_provided|Ciliary_dyskinesia|_primary|_40": 12,
    "DNAH9-related_disorder|Ciliary_dyskinesia|_primary|_40": 1,
    "Inborn_genetic_diseases|Ciliary_dyskinesia|_primary|_40|not_provided": 3,
    "not_provided|DNAH9-related_disorder|Non-immune_hydrops_fetalis": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_40|not_specified": 2,
    "Ciliary_dyskinesia|_primary|_40|not_provided|DNAH9-related_disorder": 3,
    "Ciliary_dyskinesia|_primary|_40|not_provided|Congenital_heart_disease": 1,
    "Inborn_genetic_diseases|not_provided|DNAH9-related_disorder": 4,
    "Ciliary_dyskinesia|_primary|_40|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ciliary_dyskinesia|_primary|_40": 1,
    "Ciliary_dyskinesia|_primary|_40|not_provided|Inborn_genetic_diseases": 1,
    "Hydrocephalus|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|DNAH9-related_disorder": 5,
    "Ciliary_dyskinesia|_primary|_40|not_provided|not_specified": 1,
    "DNAH9-related_disorder|not_provided|Ciliary_dyskinesia|_primary|_40": 1,
    "not_provided|not_specified|DNAH9-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Ciliary_dyskinesia|_primary|_40": 2,
    "Primary_ciliary_dyskinesia|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Ciliary_dyskinesia|_primary|_40": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_40|Sinoatrial_node_dysfunction_and_deafness": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_40|DNAH9-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_40|Primary_ciliary_dyskinesia": 1,
    "not_specified|not_provided|Ciliary_dyskinesia|_primary|_40": 1,
    "DNAH9-related_disorder|not_provided|Ciliary_dyskinesia|_primary|_40|not_specified": 1,
    "Primary_ciliary_dyskinesia_3|Inborn_genetic_diseases": 1,
    "Ciliary_dyskinesia|_primary|_40|DNAH9-related_disorder|not_provided": 1,
    "not_provided|DNAH9-related_disorder|Ciliary_dyskinesia|_primary|_40|Inborn_genetic_diseases": 1,
    "DNAH9-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|DNAH9-related_disorder|Ciliary_dyskinesia|_primary|_40": 1,
    "DNAH9-related_disorder|Inborn_genetic_diseases": 1,
    "Abnormal_cardiovascular_system_morphology|Ciliary_dyskinesia|_primary|_40": 1,
    "Ciliary_dyskinesia|_primary|_40|not_provided|Inborn_genetic_diseases|DNAH9-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_50|not_provided|Ciliary_dyskinesia|_primary|_40": 1,
    "not_provided|Inborn_genetic_diseases|Ciliary_dyskinesia|_primary|_40|Primary_ciliary_dyskinesia": 1,
    "Megabladder|_congenital": 4,
    "Prune_belly_syndrome|Megabladder|_congenital": 2,
    "not_provided|Megabladder|_congenital|not_specified": 1,
    "Megabladder|_congenital|not_specified": 2,
    "MYOCD-related_condition": 3,
    "not_specified|Seizure|Intellectual_disability": 1,
    "not_provided|MYOCD-related_condition": 1,
    "not_specified|Megabladder|_congenital": 1,
    "ARHGAP44-related_disorder": 2,
    "Combined_oxidative_phosphorylation_defect_type_17": 799,
    "Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17": 7,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_17|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_17": 17,
    "ELAC2-related_disorder|Combined_oxidative_phosphorylation_defect_type_17|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_17": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|not_provided": 39,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2|ELAC2-related_disorder": 1,
    "Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_17": 14,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_17|not_provided|Prostate_cancer|_hereditary|_2": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|Inborn_genetic_diseases": 24,
    "ELAC2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|ELAC2-related_disorder|Prostate_cancer|_hereditary|_2": 1,
    "not_provided|ELAC2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|not_specified": 11,
    "Combined_oxidative_phosphorylation_defect_type_17|not_provided|not_specified|Prostate_cancer|_hereditary|_2": 1,
    "not_specified|Combined_oxidative_phosphorylation_defect_type_17": 3,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_defect_type_17": 3,
    "not_provided|Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|Intellectual_disability": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2|not_provided|not_specified": 2,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2": 2,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_17": 2,
    "ELAC2-related_disorder|Combined_oxidative_phosphorylation_defect_type_17": 3,
    "Combined_oxidative_phosphorylation_defect_type_17|not_specified|Prostate_cancer|_hereditary|_2|ELAC2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|ELAC2-related_disorder": 4,
    "not_provided|not_specified|Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17": 1,
    "Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_17|not_provided": 6,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_17|not_specified|Prostate_cancer|_hereditary|_2": 2,
    "Combined_oxidative_phosphorylation_defect_type_17|Microcephaly": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|not_provided|Prostate_cancer|_hereditary|_2|not_specified": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2|not_provided": 3,
    "Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2|not_specified|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2|not_specified": 2,
    "Combined_oxidative_phosphorylation_defect_type_17|not_provided|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|ELAC2-related_disorder|not_provided": 1,
    "Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|not_specified|not_provided|Prostate_cancer|_hereditary|_2": 2,
    "Ovarian_cancer|Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2|_susceptibility_to": 1,
    "not_specified|not_provided|ELAC2-related_disorder|Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17": 1,
    "not_provided|Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17|ELAC2-related_disorder": 1,
    "Prostate_cancer|_hereditary|_2": 1,
    "not_provided|ELAC2-related_disorder|Combined_oxidative_phosphorylation_defect_type_17|Prostate_cancer|_hereditary|_2": 1,
    "ELAC2-related_disorder|not_provided|Inborn_genetic_diseases|Prostate_cancer|_hereditary|_2|Combined_oxidative_phosphorylation_defect_type_17": 1,
    "Ovarian_cancer|Combined_oxidative_phosphorylation_defect_type_17|not_provided|not_specified|ELAC2-related_disorder": 1,
    "Combined_oxidative_phosphorylation_defect_type_17|Ovarian_cancer": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3": 45,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_3": 7,
    "not_provided|not_specified|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_3": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_specified|not_provided": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_3": 14,
    "not_provided|Leigh_syndrome|COX10-related_disorder|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Inborn_genetic_diseases|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided": 1,
    "Leigh_syndrome|not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_specified|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Leigh_syndrome|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided|Leigh_syndrome|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Leigh_syndrome|not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided": 4,
    "COX10-related_disorder": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_specified": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_3": 1,
    "Leigh_syndrome|not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided": 1,
    "not_specified|Leigh_syndrome|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Leigh_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Inborn_genetic_diseases|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Leigh_syndrome": 1,
    "Leigh_syndrome|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_3|not_provided": 1,
    "Leigh_syndrome|COX10-related_disorder|not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_3|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Hereditary_liability_to_pressure_palsies": 12,
    "Charcot-Marie-Tooth_disease|_type_I|Hereditary_liability_to_pressure_palsies": 10,
    "Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I": 11,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_provided|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Hereditary_liability_to_pressure_palsies|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_1E|Guillain-Barre_syndrome|_familial|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease|_type_IA|Hereditary_liability_to_pressure_palsies|Dejerine-Sottas_disease": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1E|Hereditary_liability_to_pressure_palsies|Autosomal_recessive_Dejerine-Sottas_syndrome": 1,
    "Charcot-Marie-Tooth_disease|_type_IA|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Dejerine-Sottas_disease": 2,
    "not_provided|DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Hereditary_liability_to_pressure_palsies|Dejerine-Sottas_disease|Guillain-Barre_syndrome|_familial|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|not_provided|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 1,
    "Hereditary_liability_to_pressure_palsies": 4,
    "not_provided|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Roussy-L\u00e9vy_syndrome|Spasticity|Respiratory_distress|Tongue_fasciculations": 1,
    "not_specified|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Hereditary_liability_to_pressure_palsies": 1,
    "not_provided|Hereditary_liability_to_pressure_palsies|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|PMP22-related_disorder": 1,
    "Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|Guillain-Barre_syndrome|_familial|Hereditary_liability_to_pressure_palsies|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Guillain-Barre_syndrome|_familial|Hereditary_liability_to_pressure_palsies|Dejerine-Sottas_disease|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_1E": 2,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|Roussy-L\u00e9vy_syndrome|Dejerine-Sottas_disease|Guillain-Barre_syndrome|_familial|not_provided|not_specified|Charcot-Marie-Tooth_disease|_type_1a|_autosomal_recessive|Tip-toe_gait": 1,
    "Inborn_genetic_diseases|PMP22-related_disorder|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Charcot-Marie-Tooth_disease|_type_IA|Charcot-Marie-Tooth_disease|_type_I": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 1,
    "PMP22-related_disorder": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_IA": 2,
    "Charcot-Marie-Tooth_disease|Hereditary_liability_to_pressure_palsies": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2E|not_provided|Charcot-Marie-Tooth_disease|_type_I|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Charcot-Marie-Tooth_disease|_type_IA|not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_IA|Charcot-Marie-Tooth_disease_type_1E": 1,
    "Roussy-L\u00e9vy_syndrome|Dejerine-Sottas_disease|Guillain-Barre_syndrome|_familial|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|not_provided": 1,
    "not_provided|Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1E|Roussy-L\u00e9vy_syndrome|Guillain-Barre_syndrome|_familial|Charcot-Marie-Tooth_disease|_type_IA|Hereditary_liability_to_pressure_palsies|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Dejerine-Sottas_disease": 1,
    "DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|_type_IA": 5,
    "Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|_type_I": 2,
    "not_specified|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1E": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Inborn_genetic_diseases|DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|_type_IA|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_type_I|DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Guillain-Barre_syndrome|_familial|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|Dejerine-Sottas_disease|Hereditary_liability_to_pressure_palsies": 1,
    "not_provided|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_1E": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|Guillain-Barre_syndrome|_familial|Roussy-L\u00e9vy_syndrome|Dejerine-Sottas_disease|not_provided|Charcot-Marie-Tooth_disease|_type_I|not_specified": 1,
    "PMP22-related_disorder|not_specified|Charcot-Marie-Tooth_disease|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I|Tip-toe_gait|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease|_type_I|not_provided|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease|_type_1a|_with_focally_folded_myelin_sheaths": 1,
    "Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease|_type_I|not_provided|Tip-toe_gait": 1,
    "PMP22-related_disorder|Charcot-Marie-Tooth_disease|_type_I": 1,
    "PMP22-related_disorder|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I|not_specified|Charcot-Marie-Tooth_disease|Dejerine-Sottas_disease|Roussy-L\u00e9vy_syndrome|Guillain-Barre_syndrome|_familial|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "Dejerine-Sottas_disease|DEJERINE-SOTTAS_SYNDROME|_AUTOSOMAL_DOMINANT|Roussy-L\u00e9vy_syndrome|Charcot-Marie-Tooth_disease|_type_I|Inborn_genetic_diseases": 1,
    "Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I|not_provided": 1,
    "not_specified|Guillain-Barre_syndrome|_familial|Hereditary_liability_to_pressure_palsies|Roussy-L\u00e9vy_syndrome|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_1E|Charcot-Marie-Tooth_disease|_type_IA": 1,
    "not_provided|not_specified|Hereditary_liability_to_pressure_palsies|Charcot-Marie-Tooth_disease|_type_I": 1,
    "Spermatogenic_failure_81": 3,
    "Non-obstructive_azoospermia|Spermatogenic_failure_71|Ovarian_dysgenesis_10": 1,
    "Spermatogenic_failure_71": 1,
    "Infertility_disorder": 1,
    "Ovarian_dysgenesis_10": 1,
    "not_specified|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1": 2,
    "not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_1": 2,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_1|not_specified": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|not_specified": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_1|Inborn_genetic_diseases": 1,
    "TTC19-related_disorder": 1,
    "TTC19-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_2": 3,
    "not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_2": 1,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_2|Inborn_genetic_diseases": 2,
    "not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_2": 4,
    "Mitochondrial_complex_III_deficiency_nuclear_type_2|not_provided": 17,
    "Mitochondrial_complex_III_deficiency_nuclear_type_2": 54,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_2|not_specified": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_2|not_provided|TTC19-related_disorder": 2,
    "Inborn_genetic_diseases|Mitochondrial_complex_III_deficiency_nuclear_type_2": 2,
    "TTC19-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_2": 3,
    "Inborn_genetic_diseases|Mitochondrial_complex_III_deficiency_nuclear_type_2|not_provided": 2,
    "Mitochondrial_complex_III_deficiency_nuclear_type_2|not_provided|Autism": 1,
    "Mitochondrial_complex_III_deficiency_nuclear_type_2|Inborn_genetic_diseases|not_provided": 2,
    "TTC19-related_disorder|Inborn_genetic_diseases|Mitochondrial_complex_III_deficiency_nuclear_type_2|not_provided": 1,
    "Inborn_genetic_diseases|TTC19-related_disorder|not_provided|not_specified": 1,
    "TTC19-related_disorder|not_specified|Mitochondrial_complex_III_deficiency_nuclear_type_2|not_provided": 1,
    "not_specified|not_provided|Mitochondrial_complex_III_deficiency_nuclear_type_2": 1,
    "not_provided|NCOR1-related_disorder": 10,
    "NCOR1-related_disorder|not_specified|not_provided": 2,
    "NCOR1-related_disorder": 27,
    "NCOR1-related_disorder|not_provided": 6,
    "NCOR1-related_Neurodevelopmental_disorder": 1,
    "NCOR1-related_autism_spectrum_disorder": 1,
    "not_specified|NCOR1-related_disorder": 1,
    "Developmental_delay|Hyperlaxity|Thin_skin": 1,
    "CHIME_syndrome|not_provided": 5,
    "CHIME_syndrome": 20,
    "Postaxial_hand_polydactyly|Hypoplasia_of_scrotum|Low-set_ears|Bilateral_cleft_lip_and_palate|Premature_birth|Wide_intermamillary_distance|Hypertelorism|Camptodactyly_of_finger|Inborn_genetic_diseases|CHIME_syndrome": 1,
    "Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome": 1,
    "PIGL-related_disorder|not_provided|CHIME_syndrome": 1,
    "not_provided|CHIME_syndrome": 3,
    "Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome|CHIME_syndrome": 4,
    "Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome|not_specified|CHIME_syndrome|not_provided": 1,
    "Syndromic_intellectual_disability|not_provided|CHIME_syndrome": 1,
    "not_provided|CHIME_syndrome|Hyperphosphatasia_with_intellectual_disability_syndrome_1|PIGL-related_disorder": 1,
    "Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome|CHIME_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|CHIME_syndrome|Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome": 2,
    "PIGL-related_disorder|CHIME_syndrome|not_provided": 1,
    "PIGL-related_disorder|Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome|Inborn_genetic_diseases|not_provided|CHIME_syndrome|Camptodactyly_of_finger|Hypertelorism|Bilateral_cleft_lip_and_palate|Postaxial_hand_polydactyly|Wide_intermamillary_distance|Hypoplasia_of_scrotum|Premature_birth|Low-set_ears|Intellectual_disability": 1,
    "Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome|CHIME_syndrome|not_provided": 3,
    "Coloboma|_Congenital_Heart_Disease|_Ichthyosiform_Dermatosis|_Intellectual_Disability|_and_Ear_Anomalies_(CHIME)_Syndrome|not_provided|CHIME_syndrome": 1,
    "CHIME_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "PIGL-related_disorder|not_provided": 1,
    "not_provided|PIGL-related_disorder": 1,
    "Inborn_genetic_diseases|CHIME_syndrome": 1,
    "Common_Variable_Immune_Deficiency|_Dominant|not_provided": 2,
    "Common_Variable_Immune_Deficiency|_Dominant": 4,
    "Immunodeficiency|_common_variable|_2|not_specified": 3,
    "Immunodeficiency|_common_variable|_2|Common_Variable_Immune_Deficiency|_Dominant": 2,
    "Common_Variable_Immune_Deficiency|_Dominant|Immunodeficiency|_common_variable|_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Immunodeficiency|_common_variable|_2": 6,
    "not_provided|Immunodeficiency|_common_variable|_2": 15,
    "not_specified|Immunodeficiency|_common_variable|_2|Inborn_genetic_diseases|Common_Variable_Immune_Deficiency|_Dominant": 1,
    "TNFRSF13B-related_disorder|not_provided|Immunodeficiency|_common_variable|_2": 1,
    "Immunodeficiency|_common_variable|_2|TNFRSF13B-related_disorder": 5,
    "Immunodeficiency|_common_variable|_2|Inborn_genetic_diseases": 10,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_2|Common_Variable_Immune_Deficiency|_Dominant": 1,
    "Immunodeficiency|_common_variable|_2|not_provided": 11,
    "not_provided|Immunoglobulin_A_deficiency_2|Immunodeficiency|_common_variable|_2": 1,
    "Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|not_provided": 2,
    "Common_Variable_Immune_Deficiency|_Dominant|not_provided|Immunodeficiency|_common_variable|_2": 1,
    "Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2": 4,
    "Common_Variable_Immune_Deficiency|_Dominant|not_specified|not_provided|Immunodeficiency|_common_variable|_2": 1,
    "Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|Inborn_genetic_diseases|Common_Variable_Immune_Deficiency|_Dominant": 1,
    "not_specified|Immunodeficiency|_common_variable|_2|not_provided": 2,
    "Immunodeficiency|_common_variable|_2|not_provided|not_specified": 1,
    "TNFRSF13B-related_disorder|Immunodeficiency|_common_variable|_2": 4,
    "not_provided|Common_Variable_Immune_Deficiency|_Dominant|Immunodeficiency|_common_variable|_2|not_specified": 1,
    "Common_variable_immunodeficiency|Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|not_provided|See_cases": 1,
    "TNFRSF13B-related_disorder|not_specified|not_provided|Immunodeficiency|_common_variable|_2": 1,
    "not_provided|Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2": 2,
    "Immunodeficiency|_common_variable|_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency|_common_variable|_1|Immunodeficiency|_common_variable|_2": 1,
    "TNFRSF13B-related_disorder|not_specified|Immunodeficiency|_common_variable|_2": 1,
    "not_provided|Immunoglobulin_A_deficiency_2": 1,
    "not_provided|TNFRSF13B-related_disorder|Immunodeficiency|_common_variable|_1|Immunodeficiency|_common_variable|_2": 1,
    "TNFRSF13B-related_disorder|Immune_deficiency|_familial_variable|Severe_SARS-CoV-2_infection|_susceptibility_to|Common_variable_immunodeficiency|Immunodeficiency|_common_variable|_2|Immunodeficiency|_common_variable|_1|Immunoglobulin_A_deficiency_2|not_specified|not_provided": 1,
    "TNFRSF13B-related_disorder": 2,
    "Common_Variable_Immune_Deficiency|_Dominant|not_provided|Immunodeficiency|_common_variable|_2|not_specified": 1,
    "IgAD1|Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|Common_variable_immunodeficiency|not_provided": 1,
    "not_specified|not_provided|TNFRSF13B-related_disorder|Immunodeficiency|_common_variable|_2": 1,
    "Immunoglobulin_A_deficiency_2|Immunodeficiency|_common_variable|_2|not_specified|not_provided|Common_Variable_Immune_Deficiency|_Dominant": 1,
    "Immunoglobulin_A_deficiency_2|not_provided|Immunodeficiency|_common_variable|_2": 1,
    "Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|Immunodeficiency|_common_variable|_1|TNFRSF13B-related_disorder|Common_Variable_Immune_Deficiency|_Dominant|Hyper-IgM_syndrome_type_2|not_provided": 1,
    "not_provided|Immunodeficiency|_common_variable|_2|TNFRSF13B-related_disorder": 1,
    "TNFRSF13B-related_disorder|Immunodeficiency|_common_variable|_2|not_provided": 1,
    "not_provided|TNFRSF13B-related_disorder|Immunodeficiency|_common_variable|_2": 1,
    "TNFRSF13B-related_disorder|Immunodeficiency|_common_variable|_2|Common_Variable_Immune_Deficiency|_Dominant": 1,
    "not_specified|Immunodeficiency|_common_variable|_2": 2,
    "Common_Variable_Immune_Deficiency|_Dominant|not_provided|not_specified|Immunodeficiency|_common_variable|_2": 1,
    "not_specified|Immunodeficiency|_common_variable|_2|not_provided|Common_Variable_Immune_Deficiency|_Dominant": 1,
    "Common_variable_immunodeficiency|Immunodeficiency|_common_variable|_2": 1,
    "not_provided|Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|not_specified": 1,
    "Immunodeficiency|_common_variable|_2|Immunoglobulin_A_deficiency_2|Inborn_genetic_diseases": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|not_provided": 5,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 21,
    "Spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 4,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 11,
    "not_provided|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|not_provided": 3,
    "Birt-Hogg-Dube_syndrome_1": 63,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 13,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 202,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 216,
    "Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 14,
    "Birt-Hogg-Dube_syndrome": 727,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1": 24,
    "not_provided|Birt-Hogg-Dube_syndrome": 21,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 24,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 25,
    "Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 12,
    "Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 46,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 33,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 2,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1": 7,
    "Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 23,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 15,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Exstrophy-epispadias_complex": 1,
    "Birt-Hogg-Dube_syndrome|not_provided": 24,
    "Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 39,
    "Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 17,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 25,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome": 1,
    "not_provided|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma": 1,
    "Birt-Hogg-Dube_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome_1": 2,
    "Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Birt-Hogg-Dube_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 24,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 2,
    "not_provided|not_specified|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder|Familial_spontaneous_pneumothorax": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "not_specified|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Birt-Hogg-Dube_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Familial_spontaneous_pneumothorax|not_specified|FLCN-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1": 2,
    "not_provided|not_specified|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|not_provided": 1,
    "See_cases|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Familial_spontaneous_pneumothorax": 2,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Carcinoma_of_colon|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "17p11.2_microduplication_syndrome|Carcinoma_of_colon|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 2,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "FLCN-related_disorder|not_provided|not_specified|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_specified": 2,
    "Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1": 4,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Pulmonary_arterial_hypertension|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "FLCN-related_disorder|not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1": 3,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided": 15,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_provided": 2,
    "Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|17p11.2_microduplication_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|not_provided": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|not_provided|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 5,
    "Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Carcinoma_of_colon|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "not_specified|Birt-Hogg-Dube_syndrome": 3,
    "not_specified|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 1,
    "not_specified|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|FLCN-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 2,
    "Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 2,
    "FLCN-related_disorder": 22,
    "Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "not_specified|not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 4,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Chromophobe_renal_cell_carcinoma": 1,
    "Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|not_specified|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided": 2,
    "not_provided|Birt-Hogg-Dube_syndrome|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_spontaneous_pneumothorax": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 2,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|not_specified": 6,
    "Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome": 2,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Ovarian_cancer|not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Ovarian_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|not_specified": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Colorectal_cancer|not_specified|Birt-Hogg-Dube_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|not_specified|not_provided|Birt-Hogg-Dube_syndrome_1": 1,
    "17p11.2_microduplication_syndrome|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hypoparathyroidism": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1": 2,
    "Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome": 1,
    "FLCN-related_disorder|not_provided|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1": 3,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder|Birt-Hogg-Dube_syndrome": 2,
    "FLCN-related_disorder|not_provided|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "FLCN-related_disorder|Multiple_monogenic_benign_skin_tumours|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Pilocytic_astrocytoma|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|not_specified": 1,
    "Familial_spontaneous_pneumothorax|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|FLCN-related_disorder": 1,
    "not_provided|FLCN-related_disorder": 2,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "FLCN-related_disorder|not_specified": 1,
    "not_specified|FLCN-related_disorder": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|FLCN-related_disorder|not_specified": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|not_specified": 1,
    "not_specified|FLCN-related_disorder|not_provided": 1,
    "not_specified|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome": 1,
    "Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 2,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer": 1,
    "Hereditary_renal_cancer|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1": 2,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome|FLCN-related_disorder|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 2,
    "17p11.2_microduplication_syndrome|Carcinoma_of_colon|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Colorectal_cancer|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Colorectal_cancer|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Birt-Hogg-Dube_syndrome": 1,
    "not_specified|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_specified|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder": 2,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "not_provided|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Familial_spontaneous_pneumothorax": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|FLCN-related_disorder|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_specified|Familial_spontaneous_pneumothorax|FLCN-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_specified|not_provided": 1,
    "Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Colorectal_cancer|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided|not_specified": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Carcinoma_of_colon|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome": 2,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|not_specified|not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "not_specified|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|not_provided|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Birt-Hogg-Dube_syndrome|Ovarian_cancer|not_provided": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 2,
    "Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Hepatoblastoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|not_specified|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|17p11.2_microduplication_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|FLCN-related_disorder|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 2,
    "not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "FLCN-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Birt-Hogg-Dube_syndrome": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Carcinoma_of_colon|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_specified": 1,
    "not_provided|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome": 1,
    "Familial_spontaneous_pneumothorax|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome|17p11.2_microduplication_syndrome|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder|Familial_spontaneous_pneumothorax|Carcinoma_of_colon|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Birt-Hogg-Dube_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Colorectal_cancer|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Hereditary_cancer-predisposing_syndrome|FLCN-related_disorder|not_provided": 1,
    "Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome_1|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|17p11.2_microduplication_syndrome|Familial_spontaneous_pneumothorax|Colorectal_cancer": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Colorectal_cancer|17p11.2_microduplication_syndrome|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome|Birt-Hogg-Dube_syndrome|not_specified": 1,
    "Birt-Hogg-Dube_syndrome|not_provided|Birt-Hogg-Dube_syndrome_1|17p11.2_microduplication_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_spontaneous_pneumothorax|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome|Colorectal_cancer|17p11.2_microduplication_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|not_provided|Birt-Hogg-Dube_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Birt-Hogg-Dube_syndrome|Birt-Hogg-Dube_syndrome_1": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|17p11.2_microduplication_syndrome|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|FLCN-related_disorder|Birt-Hogg-Dube_syndrome_1|not_provided": 1,
    "Birt-Hogg-Dube_syndrome_1|not_specified": 1,
    "Birt-Hogg-Dube_syndrome_1|not_specified|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 1,
    "not_provided|Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax": 3,
    "not_provided|Birt-Hogg-Dube_syndrome|not_specified|Familial_spontaneous_pneumothorax|Hereditary_cancer-predisposing_syndrome": 1,
    "Birt-Hogg-Dube_syndrome|not_specified|Familial_spontaneous_pneumothorax": 2,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|FLCN-related_disorder": 1,
    "not_provided|Colorectal_cancer|Nonpapillary_renal_cell_carcinoma|Birt-Hogg-Dube_syndrome_1|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|FLCN-related_disorder": 1,
    "FLCN-related_disorder|Familial_spontaneous_pneumothorax|Birt-Hogg-Dube_syndrome|not_provided": 1,
    "Birt-Hogg-Dube_syndrome|Familial_spontaneous_pneumothorax|not_provided|Nonpapillary_renal_cell_carcinoma|Colorectal_cancer|Birt-Hogg-Dube_syndrome_1|FLCN-related_disorder": 1,
    "Smith-Magenis_syndrome": 70,
    "RAI1-related_disorder": 138,
    "not_specified|RAI1-related_disorder|not_provided": 1,
    "not_provided|Smith-Magenis_syndrome": 10,
    "RAI1-related_disorder|not_provided": 127,
    "not_specified|Inborn_genetic_diseases|RAI1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|RAI1-related_disorder": 20,
    "RAI1-related_disorder|Inborn_genetic_diseases|not_provided": 43,
    "Inborn_genetic_diseases|not_provided|Smith-Magenis_syndrome|RAI1-related_disorder|not_specified": 1,
    "not_provided|RAI1-related_disorder": 120,
    "Inborn_genetic_diseases|not_provided|See_cases|Developmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|RAI1-related_disorder": 12,
    "RAI1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 5,
    "RAI1-related_disorder|not_provided|Inborn_genetic_diseases": 19,
    "not_provided|not_specified|Inborn_genetic_diseases|RAI1-related_disorder": 1,
    "not_provided|RAI1-related_disorder|not_specified": 3,
    "Inborn_genetic_diseases|RAI1-related_disorder|Smith-Magenis_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Smith-Magenis_syndrome|not_provided|RAI1-related_disorder": 3,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Smith-Magenis_syndrome": 4,
    "Inborn_genetic_diseases|Smith-Magenis_syndrome": 6,
    "not_provided|RAI1-related_disorder|Inborn_genetic_diseases": 26,
    "not_provided|Intellectual_disability|RAI1-related_disorder|Inborn_genetic_diseases": 1,
    "RAI1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 8,
    "Inborn_genetic_diseases|not_provided|Smith-Magenis_syndrome": 2,
    "Smith-Magenis_syndrome|not_provided": 9,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_provided": 23,
    "Smith-Magenis_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "RAI1-related_disorder|not_provided|not_specified": 5,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_specified|not_provided|Smith-Magenis_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Smith-Magenis_syndrome|RAI1-related_disorder": 2,
    "RAI1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_specified|not_provided|Intellectual_disability": 1,
    "RAI1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Smith-Magenis_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|History_of_neurodevelopmental_disorder|RAI1-related_disorder": 1,
    "not_provided|Intellectual_disability|RAI1-related_disorder": 1,
    "not_specified|not_provided|Smith-Magenis_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Smith-Magenis_syndrome|not_specified|not_provided": 2,
    "not_specified|RAI1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|RAI1-related_disorder": 2,
    "not_provided|RAI1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Smith-Magenis_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "RAI1-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Smith-Magenis_syndrome": 2,
    "RAI1-related_disorder|Smith-Magenis_syndrome|not_provided": 1,
    "not_specified|RAI1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|RAI1-related_disorder": 3,
    "RAI1-related_disorder|not_provided|not_specified|Smith-Magenis_syndrome": 1,
    "not_provided|Smith-Magenis_syndrome|RAI1-related_disorder": 4,
    "not_specified|not_provided|RAI1-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Smith-Magenis_syndrome": 2,
    "RAI1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 4,
    "not_specified|Smith-Magenis_syndrome": 1,
    "RAI1-related_disorder|not_specified": 1,
    "RAI1-related_disorder|Smith-Magenis_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Smith-Magenis_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|RAI1-related_disorder|Inborn_genetic_diseases": 1,
    "17p11.2_microduplication_syndrome|Smith-Magenis_syndrome|RAI1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RAI1-related_disorder|not_provided|Inborn_genetic_diseases|Smith-Magenis_syndrome": 1,
    "Smith-Magenis_syndrome|Intellectual_disability": 1,
    "RAI1-related_disorder|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|Vascular_disorder": 1,
    "Inborn_genetic_diseases|RAI1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|RAI1-related_disorder": 1,
    "not_provided|RAI1-related_disorder|Smith-Magenis_syndrome": 1,
    "RAI1-related_disorder|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Smith-Magenis_syndrome|not_specified": 1,
    "not_specified|not_provided|RAI1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Smith-Magenis_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_provided|Smith-Magenis_syndrome": 1,
    "not_specified|RAI1-related_disorder|not_provided|Smith-Magenis_syndrome": 1,
    "RAI1-related_disorder|Deafness|Smith-Magenis_syndrome|PMP22-RAI1_contiguous_gene_duplication_syndrome|not_provided": 1,
    "Smith-Magenis_syndrome|RAI1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RAI1-related_disorder|Inborn_genetic_diseases|not_provided|Smith-Magenis_syndrome": 2,
    "Inborn_genetic_diseases|RAI1-related_disorder|not_provided|not_specified|Smith-Magenis_syndrome": 1,
    "Smith-Magenis_syndrome|not_provided|RAI1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Smith-Magenis_syndrome|not_provided|RAI1-related_disorder": 1,
    "not_provided|Smith-Magenis_syndrome|RAI1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|RAI1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|RAI1-related_disorder|Inborn_genetic_diseases|Smith-Magenis_syndrome|not_specified": 1,
    "Smith-Magenis_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Smith-Magenis_syndrome|RAI1-related_disorder": 1,
    "Smith-Magenis_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|RAI1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "RAI1-related_disorder|Smith-Magenis_syndrome": 1,
    "Smith-Magenis_syndrome|Developmental_disorder|not_provided": 1,
    "RAI1-related_disorder|not_provided|Smith-Magenis_syndrome": 1,
    "PMP22-RAI1_contiguous_gene_duplication_syndrome|Smith-Magenis_syndrome|not_provided": 1,
    "RAI1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_9": 1,
    "Inborn_genetic_diseases|not_specified|See_cases|RAI1-related_disorder|not_provided": 1,
    "Smith-Magenis_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|RAI1-related_disorder": 1,
    "RAI1-related_disorder|Inborn_genetic_diseases|Smith-Magenis_syndrome|not_specified|not_provided": 1,
    "IFAP_syndrome_2|Hereditary_mucoepithelial_dysplasia": 6,
    "Inborn_genetic_diseases|Obesity": 1,
    "Inborn_genetic_diseases|SREBF1-related_disorder": 1,
    "IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome|IFAP_syndrome_2": 2,
    "Hereditary_mucoepithelial_dysplasia|not_provided": 1,
    "Hereditary_mucoepithelial_dysplasia|IFAP_syndrome_2|not_provided|IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome": 1,
    "Inborn_genetic_diseases|Hereditary_mucoepithelial_dysplasia|IFAP_syndrome_2": 1,
    "Hereditary_mucoepithelial_dysplasia|IFAP_syndrome_2|Inborn_genetic_diseases": 1,
    "Hereditary_mucoepithelial_dysplasia": 2,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1": 25,
    "not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1": 10,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1|not_specified": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1|not_provided": 3,
    "ATPAF2-related_disorder|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1|not_specified": 1,
    "not_specified|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1": 2,
    "ATPAF2-related_disorder|not_specified|not_provided": 1,
    "ATPAF2-related_disorder|not_specified|not_provided|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1": 1,
    "ATPAF2-related_disorder|not_provided": 1,
    "not_specified|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_1|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 116,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 57,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified": 17,
    "not_provided|MYO15A-related_disorder": 10,
    "MYO15A-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_impairment": 3,
    "MYO15A-related_disorder|not_provided": 11,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 16,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 5,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases|MYO15A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 8,
    "MYO15A-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 12,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 23,
    "MYO15A-related_disorder|not_specified|not_provided": 4,
    "not_provided|Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3": 5,
    "MYO15A-related_disorder|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Nonsyndromic_genetic_hearing_loss|Hearing_impairment|not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3|Rare_genetic_deafness": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Rare_genetic_deafness": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided|MYO15A-related_disorder": 2,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases": 2,
    "MYO15A-related_disorder": 5,
    "MYO15A-related_disorder|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "MYO15A-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_specified|Nonsyndromic_genetic_hearing_loss|not_provided|MYO15A-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3": 8,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified|not_provided": 13,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 15,
    "MYO15A-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|MYO15A-related_disorder": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder": 2,
    "not_provided|not_specified|Nonsyndromic_genetic_hearing_loss": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 3,
    "MYO15A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided|not_specified": 16,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided|Hearing_impairment": 1,
    "Childhood_onset_hearing_loss|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases|not_specified": 1,
    "MYO15A-related_disorder|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder": 1,
    "not_provided|MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|MYO15A-related_disorder|not_specified": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified|MYO15A-related_disorder": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_impairment": 1,
    "MYO15A-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "Hearing_loss|_autosomal_recessive|not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder|Nonsyndromic_genetic_hearing_loss": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_loss|_autosomal_recessive|Hearing_impairment": 1,
    "Inborn_genetic_diseases|MYO15A-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_loss|_autosomal_recessive": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases|not_provided": 2,
    "MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified": 1,
    "not_provided|Childhood_onset_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "MYO15A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 2,
    "MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided|MYO15A-related_disorder|Ear_malformation": 1,
    "Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness": 1,
    "Rare_genetic_deafness|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Monogenic_hearing_loss|Rare_genetic_deafness": 1,
    "not_specified|not_provided|Childhood_onset_hearing_loss": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided|not_specified|Ear_malformation": 1,
    "Rare_genetic_deafness|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Nonsyndromic_genetic_hearing_loss|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|Deafness|_with_smith-magenis_syndrome": 1,
    "not_provided|Hearing_loss|_autosomal_recessive|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 4,
    "MYO15A-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Rare_genetic_deafness|Congenital_sensorineural_hearing_impairment|not_provided|MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3|Intellectual_disability": 1,
    "MYO15A-related_disorder|Rare_genetic_deafness|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_loss|_autosomal_recessive": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Rare_genetic_deafness": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_3|Rare_genetic_deafness|not_provided|Monogenic_hearing_loss|Hearing_impairment": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_impairment": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Congenital_sensorineural_hearing_impairment": 1,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder": 1,
    "MYO15A-related_disorder|not_provided|not_specified": 1,
    "Hearing_loss|_autosomal_recessive|Congenital_sensorineural_hearing_impairment|not_provided": 1,
    "MYO15A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|Hearing_impairment": 1,
    "MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Rare_genetic_deafness|not_provided|MYO15A-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases": 1,
    "not_provided|MYO15A-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|MYO15A-related_disorder|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|not_specified|Nonsyndromic_genetic_hearing_loss|MYO15A-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|MYO15A-related_disorder|Inborn_genetic_diseases": 1,
    "Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Intellectual_disability|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Inborn_genetic_diseases": 1,
    "MYO15A-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_3|Hearing_impairment": 1,
    "not_specified|not_provided|MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|Monogenic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_3": 1,
    "not_provided|MYO15A-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|MYO15A-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_3|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|not_specified|not_provided|Inborn_genetic_diseases|MYO15A-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_3|Sensorineural_hearing_loss_disorder": 1,
    "Cardiomyopathy|_dilated|_2j|Primary_dilated_cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_2j": 2,
    "Marfan_syndrome|Cardiomyopathy|_dilated|_2j": 1,
    "Combined_oxidative_phosphorylation_deficiency_49": 1,
    "Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2": 6,
    "not_provided|TOP3A-related_disorder": 5,
    "TOP3A-related_disorder|not_provided": 14,
    "TOP3A-related_disorder|Inborn_genetic_diseases|Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5|not_provided": 1,
    "Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|not_provided": 3,
    "TOP3A-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|Inborn_genetic_diseases": 1,
    "TOP3A-related_disorder": 4,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5|Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|not_provided": 5,
    "Inborn_genetic_diseases|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5|Inborn_genetic_diseases": 1,
    "TOP3A-related_disorder|not_provided|not_specified": 1,
    "Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5|not_provided": 2,
    "not_specified|TOP3A-related_disorder|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5": 3,
    "Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5": 1,
    "not_provided|Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2": 1,
    "not_provided|Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5": 2,
    "Microcephaly|_growth_restriction|_and_increased_sister_chromatid_exchange_2|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_recessive_5|TOP3A-related_disorder|not_provided": 1,
    "TOP3A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "GRAP-related_disorder": 3,
    "Hearing_loss|_autosomal_recessive_114": 1,
    "Joubert_syndrome_27|not_provided|Meckel_syndrome|_type_9": 2,
    "Meckel_syndrome|_type_9|Joubert_syndrome_27": 1,
    "not_specified|B9D1-related_disorder|Joubert_syndrome_27|not_provided": 1,
    "not_provided|B9D1-related_disorder": 1,
    "Meckel_syndrome|_type_9|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_9|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome_27|B9D1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_9": 1,
    "Joubert_syndrome_27|Meckel_syndrome|_type_9": 1,
    "Joubert_syndrome_27": 5,
    "Meckel_syndrome|_type_9|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_9": 1,
    "not_provided|Ciliopathy": 1,
    "B9D1-related_disorder": 4,
    "Joubert_syndrome_27|not_provided|not_specified|Meckel_syndrome|_type_9": 1,
    "not_provided|Ciliopathy|Joubert_syndrome_27|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_27|Joubert_syndrome": 1,
    "not_specified|Meckel_syndrome|_type_9|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 2,
    "B9D1-related_disorder|Ciliopathy": 1,
    "Meckel_syndrome|_type_9|Joubert_syndrome_27|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Joubert_syndrome_27|B9D1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "Meckel_syndrome|_type_9|Joubert_syndrome_and_related_disorders": 1,
    "Joubert_syndrome_27|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Joubert_syndrome_and_related_disorders": 1,
    "B9D1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_27|not_specified|Joubert_syndrome|Meckel_syndrome|_type_9": 1,
    "Meckel_syndrome|_type_9|not_provided": 1,
    "B9D1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_9": 1,
    "not_specified|not_provided|Meckel_syndrome|_type_9": 1,
    "not_specified|Meckel_syndrome|_type_9": 1,
    "B9D1-related_disorder|not_provided": 1,
    "Scoliosis|_isolated|_susceptibility_to|_1": 5,
    "Sj\u00f6gren-Larsson_syndrome": 147,
    "Sj\u00f6gren-Larsson_syndrome|not_provided": 44,
    "Sj\u00f6gren-Larsson_syndrome|not_specified": 1,
    "not_provided|Sj\u00f6gren-Larsson_syndrome": 48,
    "not_provided|Sj\u00f6gren-Larsson_syndrome|ALDH3A2-related_disorder": 2,
    "ALDH3A2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Sj\u00f6gren-Larsson_syndrome": 3,
    "ALDH3A2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Sj\u00f6gren-Larsson_syndrome": 2,
    "not_provided|not_specified|Sj\u00f6gren-Larsson_syndrome": 1,
    "not_provided|ALDH3A2-related_disorder": 2,
    "ALDH3A2-related_disorder": 1,
    "Sj\u00f6gren-Larsson_syndrome|not_specified|not_provided": 1,
    "Sj\u00f6gren-Larsson_syndrome|Cerebral_palsy|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Sj\u00f6gren-Larsson_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Sj\u00f6gren-Larsson_syndrome": 1,
    "not_provided|ALDH3A2-related_disorder|Sj\u00f6gren-Larsson_syndrome": 1,
    "ALDH3A2-related_disorder|not_specified|not_provided|Sj\u00f6gren-Larsson_syndrome": 1,
    "ALDH3A2-related_disorder|Sj\u00f6gren-Larsson_syndrome|not_specified": 1,
    "not_specified|Sj\u00f6gren-Larsson_syndrome|not_provided": 1,
    "AKAP10-related_disorder|Reclassified_-_variant_of_unknown_significance": 1,
    "AKAP10-related_disorder": 7,
    "not_specified|MAP2K3-related_disorder": 2,
    "KCNJ12-related_disorder": 47,
    "KCNJ18-related_disorder": 3,
    "Thyrotoxic_periodic_paralysis|_susceptibility_to|_2": 6,
    "not_provided|NOS2-related_disorder": 3,
    "NOS2-related_disorder": 4,
    "NOS2-related_disorder|not_provided": 1,
    "not_specified|NOS2-related_disorder": 4,
    "NOS2-related_disorder|not_specified": 1,
    "Malaria|_severe|_resistance_to": 1,
    "Malaria|_resistance_to": 1,
    "repeat_number_of_microsatellite": 1,
    "TMEM199-related_disorder": 2,
    "not_provided|TMEM199-CDG|Congenital_disorders_of_glycosylation_type_II": 1,
    "TMEM199-related_disorder|not_provided": 2,
    "TMEM199-CDG": 2,
    "TMEM199-related_disorder|TMEM199-CDG|not_provided|Congenital_disorders_of_glycosylation_type_II": 1,
    "not_provided|TMEM199-CDG": 1,
    "VTN-related_disorder": 10,
    "VTN-related_disorder|not_provided": 2,
    "VTN-related_disorder|not_specified|not_provided": 1,
    "TMEM199-CDG|not_provided": 1,
    "Congenital_defect_of_folate_absorption|not_provided": 17,
    "Congenital_defect_of_folate_absorption": 107,
    "not_provided|Congenital_defect_of_folate_absorption": 16,
    "SLC46A1-related_disorder|not_specified|not_provided": 1,
    "Congenital_defect_of_folate_absorption|not_specified": 1,
    "not_specified|Congenital_defect_of_folate_absorption": 1,
    "Inborn_genetic_diseases|SLC46A1-related_disorder|not_provided|Congenital_defect_of_folate_absorption": 2,
    "SLC46A1-related_disorder|not_provided": 2,
    "Congenital_defect_of_folate_absorption|SLC46A1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_defect_of_folate_absorption": 3,
    "not_provided|not_specified|Congenital_defect_of_folate_absorption|SLC46A1-related_disorder": 1,
    "not_provided|SLC46A1-related_disorder": 2,
    "SLC46A1-related_disorder|not_specified|not_provided|Congenital_defect_of_folate_absorption": 1,
    "Congenital_defect_of_folate_absorption|Inborn_genetic_diseases|Intellectual_disability|not_specified|not_provided": 1,
    "not_provided|Congenital_defect_of_folate_absorption|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_defect_of_folate_absorption": 2,
    "not_specified|not_provided|Congenital_defect_of_folate_absorption": 1,
    "Congenital_defect_of_folate_absorption|Inborn_genetic_diseases|not_provided|SLC46A1-related_disorder": 1,
    "SLC46A1-related_disorder": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 605,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_specified": 4,
    "Inborn_genetic_diseases|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 34,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|Inborn_genetic_diseases": 16,
    "T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant": 2,
    "T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 12,
    "not_specified|not_provided|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_provided|not_specified|FOXN1-related_disorder": 1,
    "not_provided|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 8,
    "not_specified|Autism": 2,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|Inborn_genetic_diseases|FOXN1-related_disorder": 1,
    "not_provided|FOXN1-related_disorder|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "not_specified|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_provided": 6,
    "FOXN1-related_disorder|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_provided": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_provided": 11,
    "Severe_combined_immunodeficiency_disease|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 2,
    "See_cases|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|FOXN1-related_disorder": 6,
    "FOXN1-related_disorder": 3,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "FOXN1-related_disorder|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 3,
    "not_specified|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 5,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_specified|not_provided": 2,
    "FOXN1-related_disorder|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_specified": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|Inborn_genetic_diseases|not_provided": 3,
    "Severe_combined_immunodeficiency_disease|T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "not_provided|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_specified": 1,
    "Inborn_genetic_diseases|T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_provided": 1,
    "T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|not_provided|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 3,
    "T-lymphocyte_deficiency|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 2,
    "T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-CELL_LYMPHOPENIA|_INFANTILE|_WITHOUT_NAIL_DYSTROPHY|_AUTOSOMAL_DOMINANT|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant": 6,
    "not_provided|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|Inborn_genetic_diseases": 2,
    "T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|not_provided": 1,
    "not_provided|FOXN1-related_disorder": 1,
    "not_provided|T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|FOXN1-related_disorder|not_provided": 1,
    "FOXN1-related_disorder|Inborn_genetic_diseases|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy": 1,
    "not_provided|T-cell_lymphopenia|_infantile|_with_or_without_nail_dystrophy|_autosomal_dominant|T-cell_immunodeficiency|_congenital_alopecia|_and_nail_dystrophy|FOXN1-related_disorder": 1,
    "not_provided|Cone-rod_dystrophy|Idiopathic_CD4_lymphocytopenia|not_specified": 1,
    "Cone-rod_dystrophy_24": 1,
    "UNC119-related_disorder|Cone-rod_dystrophy|not_provided": 2,
    "Macular_dystrophy|Cone-rod_dystrophy_24": 1,
    "Cone-rod_dystrophy|not_specified|not_provided": 2,
    "UNC119-related_disorder|Cone-rod_dystrophy|Idiopathic_CD4_lymphocytopenia|not_provided": 1,
    "UNC119-related_disorder|not_provided": 2,
    "not_provided|not_specified|Cone-rod_dystrophy": 1,
    "not_provided|UNC119-related_disorder": 1,
    "Idiopathic_CD4_lymphocytopenia|not_provided": 1,
    "UNC119-related_disorder|not_provided|Cone-rod_dystrophy|not_specified": 1,
    "not_provided|Cone-rod_dystrophy|not_specified": 1,
    "UNC119-related_disorder": 1,
    "Cone-rod_dystrophy_24|not_provided": 1,
    "UNC119-related_disorder|not_specified|not_provided": 1,
    "not_specified|Idiopathic_CD4_lymphocytopenia|not_provided|Cone-rod_dystrophy": 1,
    "PIGS-related_disorder": 5,
    "PIGS-related_disorder|not_provided": 6,
    "not_provided|PIGS-related_disorder": 4,
    "Glycosylphosphatidylinositol_biosynthesis_defect_18": 15,
    "Glycosylphosphatidylinositol_biosynthesis_defect_18|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Glycosylphosphatidylinositol_biosynthesis_defect_18": 1,
    "Jeune_thoracic_dystrophy|Orofaciodigital_syndrome_20": 2,
    "Orofaciodigital_syndrome_20": 3,
    "Orofaciodigital_syndrome_20|not_specified": 1,
    "Nephronophthisis_9|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2|NEK8-related_disorder": 1,
    "Nephronophthisis_9": 163,
    "Nephronophthisis_9|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2|Inborn_genetic_diseases": 2,
    "Renal-hepatic-pancreatic_dysplasia_2": 12,
    "Nephronophthisis_9|Inborn_genetic_diseases": 10,
    "Nephronophthisis_9|not_provided": 6,
    "Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|Polycystic_kidney_disease_8": 63,
    "Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|Polycystic_kidney_disease_8": 5,
    "not_provided|Nephronophthisis_9|Polycystic_kidney_disease_8|Familial_cystic_renal_disease": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|not_provided": 2,
    "Polycystic_kidney_disease_8|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis_9|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2": 3,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2": 10,
    "not_provided|Nephronophthisis_9": 7,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8": 1,
    "Inborn_genetic_diseases|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8": 2,
    "Nephronophthisis_9|not_provided|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Inborn_genetic_diseases": 1,
    "Nephronophthisis_9|Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9": 7,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|not_provided": 1,
    "NEK8-related_disorder|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|not_provided|not_specified": 1,
    "NEK8-related_disorder|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Nephronophthisis_9|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2": 7,
    "Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|Inborn_genetic_diseases": 1,
    "Polycystic_kidney_disease_8|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|not_provided": 1,
    "Nephronophthisis_9|Inborn_genetic_diseases|NEK8-related_disorder": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Nephronophthisis_9|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9": 1,
    "NEK8-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Nephronophthisis_9|Inborn_genetic_diseases": 1,
    "NEK8-related_disorder|Nephronophthisis_9": 1,
    "NEK8-related_disorder|not_provided|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Nephronophthisis_9|Inborn_genetic_diseases|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Polycystic_kidney_disease_8|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2": 5,
    "not_provided|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Nephronophthisis_9|not_specified": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Nephronophthisis_9|not_provided": 1,
    "NEK8-related_disorder": 6,
    "Nephronophthisis_9|Premature_ovarian_insufficiency|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Inborn_genetic_diseases|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9": 1,
    "Nephronophthisis_9|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2|Familial_cystic_renal_disease": 1,
    "not_specified|not_provided|Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9": 1,
    "Inborn_genetic_diseases|Nephronophthisis_9": 2,
    "not_provided|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Inborn_genetic_diseases": 1,
    "NEK8-related_disorder|not_provided|Nephronophthisis_9|Kidney_disorder": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|Polycystic_kidney_disease_8|not_provided": 1,
    "Inborn_genetic_diseases|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|NEK8-related_disorder": 1,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Inborn_genetic_diseases": 2,
    "Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|NEK8-related_disorder": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Nephronophthisis_9": 2,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "not_provided|Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Nephronophthisis_9": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|Nephronophthisis|Kidney_disorder": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Nephronophthisis_9|Inborn_genetic_diseases": 3,
    "not_specified|Nephronophthisis_9": 1,
    "not_provided|Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Premature_ovarian_insufficiency|NEK8-related_disorder": 1,
    "Nephronophthisis_9|not_provided|NEK8-related_disorder": 1,
    "Nephronophthisis_9|Inborn_genetic_diseases|Polycystic_kidney_disease_8|Renal-hepatic-pancreatic_dysplasia_2": 1,
    "Renal-hepatic-pancreatic_dysplasia_2|Polycystic_kidney_disease_8|Nephronophthisis_9|Inborn_genetic_diseases": 1,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|not_provided|NEK8-related_disorder": 1,
    "not_provided|Kidney_failure": 2,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Inborn_genetic_diseases|NEK8-related_disorder": 1,
    "Nephronophthisis_9|not_provided|not_specified": 1,
    "Nephronophthisis_9|Renal-hepatic-pancreatic_dysplasia_2|Inborn_genetic_diseases": 2,
    "ERAL1-related_disorder": 8,
    "Perrault_syndrome_6": 2,
    "Perrault_syndrome_6|Perrault_syndrome": 1,
    "not_provided|Perrault_syndrome_6": 1,
    "PHF12-related_disorder": 6,
    "MYO18A-related_disorder": 7,
    "MYO18A-related_disorder|not_provided": 1,
    "Multiple_joint_contractures|Hydrops_fetalis|Abnormal_facial_shape": 1,
    "Hereditary_hemochromatosis|not_specified": 2,
    "CRYBA1-related_disorder": 2,
    "Cataract_10_multiple_types": 33,
    "not_specified|Cataract_10_multiple_types|not_provided": 1,
    "CRYBA1-related_disorder|Cataract_10_multiple_types": 1,
    "not_specified|not_provided|Cataract_10_multiple_types": 1,
    "Inborn_genetic_diseases|Cataract_10_multiple_types": 2,
    "not_provided|Cataract_10_multiple_types|CRYBA1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|CRYBA1-related_disorder|Cataract_10_multiple_types": 1,
    "Cataract_10_multiple_types|CRYBA1-related_disorder": 1,
    "Cataract_10_multiple_types|not_provided|not_specified": 1,
    "not_provided|Cataract_10_multiple_types": 1,
    "not_provided|not_specified|Cataract_10_multiple_types": 1,
    "Cataract_10_multiple_types|not_specified": 1,
    "Cataract_10_multiple_types|not_provided": 1,
    "Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities": 47,
    "not_provided|TAOK1-related_disorder": 4,
    "not_provided|Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities": 2,
    "TAOK1-related_disorder": 18,
    "DEVELOPMENTAL_DELAY_WITHOUT_INTELLECTUAL_IMPAIRMENT_OR_BEHAVIORAL_ABNORMALITIES|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TAOK1-related_disorder": 1,
    "Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities|not_provided": 3,
    "Global_developmental_delay|Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities": 1,
    "TAOK1-related_disorder|Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities": 1,
    "TAOK1-related_disorder|not_provided": 3,
    "Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities|DEVELOPMENTAL_DELAY_WITHOUT_INTELLECTUAL_IMPAIRMENT_OR_BEHAVIORAL_ABNORMALITIES": 1,
    "not_provided|Neurodevelopmental_disorder|Macroglossia|Global_developmental_delay|Short_5th_finger|Abnormality_of_the_face": 1,
    "TAOK1-related_disorder|Inborn_genetic_diseases": 1,
    "TAOK1-related_neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder|Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities": 1,
    "TAOK1-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities|not_provided|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder|Developmental_delay_with_or_without_intellectual_impairment_or_behavioral_abnormalities|See_cases|not_provided": 1,
    "GIT1-related_disorder": 13,
    "not_provided|GIT1-related_disorder": 2,
    "EFCAB5-related_disorder": 23,
    "not_provided|EFCAB5-related_disorder": 1,
    "not_specified|EFCAB5-related_disorder": 2,
    "Neurodevelopmental_disorder_with_spasticity|_seizures|_and_brain_abnormalities|not_provided|Microcephaly|Seizure|Spasticity|Severe_global_developmental_delay": 1,
    "NSRP1-related_disorder|not_provided": 1,
    "not_specified|Neurodevelopmental_disorder_with_spasticity|_seizures|_and_brain_abnormalities": 1,
    "Neurodevelopmental_disorder_with_spasticity|_seizures|_and_brain_abnormalities": 2,
    "Neurodevelopmental_disorder_with_spasticity|_seizures|_and_brain_abnormalities|Microcephaly|Seizure|Spasticity|Severe_global_developmental_delay": 2,
    "Behavior_disorder": 85,
    "not_provided|Behavior_disorder": 17,
    "Behavior_disorder|not_provided": 8,
    "SLC6A4-related_disorder": 4,
    "Obsessive-compulsive_disorder": 2,
    "SLC6A4-related_disorder|Behavior_disorder": 2,
    "Obsessive-compulsive_disorder|_susceptibility_to|Behavior_disorder": 1,
    "Autism_spectrum_disorder|Serotonin_transporter_activity|_increased/decreased": 1,
    "Alzheimer_disease_type_1|not_provided": 3,
    "ATAD5-related_disorder": 28,
    "not_specified|ATAD5-related_disorder": 1,
    "not_provided|ATAD5-related_disorder": 4,
    "ATAD5-related_disorder|not_provided": 3,
    "ATAD5-related_disorder|not_specified": 1,
    "RNF135-related_disorder": 5,
    "RNF135-related_disorder|not_specified|not_provided": 1,
    "not_specified|RNF135-related_disorder|not_provided": 1,
    "Chromosome_17q11.2_deletion_syndrome|_1.4Mb": 1,
    "not_provided|RNF135-related_disorder": 1,
    "Macrocephaly|_macrosomia|_facial_dysmorphism_syndrome": 3,
    "Macrocephaly|_macrosomia|_facial_dysmorphism_syndrome|Autism_spectrum_disorder": 1,
    "not_provided|RNF135-related_disorder|not_specified": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 4,
    "Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 47,
    "Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder": 28,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2295,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1105,
    "Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 25,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 76,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 35,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_provided": 60,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1": 102,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 290,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 24,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 560,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia": 3,
    "Neurofibromatosis|_type_1|not_provided": 243,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 157,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 654,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 631,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 27,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 7,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 105,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Abnormality_of_the_skin": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 640,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 83,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 33,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 2,
    "Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 15,
    "Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 38,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 7,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1": 13,
    "NF1-related_disorder": 70,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 9,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 6,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|not_specified": 1,
    "not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|not_specified": 1,
    "not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 62,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 3,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 5,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_specified": 1,
    "Spinal_neurofibroma": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 5,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia": 9,
    "Juvenile_myelomonocytic_leukemia|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 23,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 13,
    "NF1-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_specified": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_specified": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 22,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 23,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 257,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer|not_provided|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 33,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 3,
    "not_provided|not_specified|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 9,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 33,
    "not_provided|Neurofibromatosis|_type_1|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Neurofibromatosis|_type_1": 41,
    "Gastric_cancer|NF1-related_disorder|Neurofibromatosis|_type_1|not_provided": 1,
    "Tibial_pseudarthrosis|Neurofibromatosis|_type_1": 14,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|not_specified": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "not_specified|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|not_provided|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 4,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis|_type_1": 10,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 12,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 47,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1": 4,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_provided": 3,
    "Juvenile_myelomonocytic_leukemia": 75,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 2,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Tibial_pseudarthrosis|Neurofibromatosis|_type_1": 2,
    "not_provided|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 5,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|NF1-related_disorder|not_specified|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 5,
    "Hereditary_cancer-predisposing_syndrome|Chromosome_17q11.2_deletion_syndrome|_1.4Mb|not_specified|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 3,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 3,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 9,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia": 4,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 9,
    "Malignant_tumor_of_urinary_bladder|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 1,
    "not_specified|Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 6,
    "not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|Neurofibromatosis|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder": 8,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 34,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 6,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Juvenile_myelomonocytic_leukemia|not_provided|Neurofibromatosis|_type_1": 5,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Gastric_cancer": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Tibial_pseudarthrosis|Neurofibromatosis|_type_1|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Tibial_pseudarthrosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|NF1-related_disorder|not_provided|Juvenile_myelomonocytic_leukemia": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 7,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis|_type_1": 15,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis|_type_1|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 337,
    "Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Inborn_genetic_diseases|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_pheochromocytoma-paraganglioma|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibroma|Juvenile_myelomonocytic_leukemia|Cafe_au_lait_spots|_multiple|Focal_T2_hyperintense_basal_ganglia_lesion|Axillary_freckling|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Neurofibromatosis|_type_1": 4,
    "not_provided|Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 7,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_specified": 5,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 4,
    "Cafe_au_lait_spots|_multiple": 3,
    "not_specified|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Tibial_pseudarthrosis|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Abnormality_of_the_skin|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|not_specified|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Tibial_pseudarthrosis": 1,
    "not_provided|not_specified|Neurofibromatosis|_familial_spinal": 1,
    "not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 8,
    "not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|not_provided": 1,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1": 13,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1": 10,
    "not_provided|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome": 1,
    "Neurofibromatosis|_type_1|not_specified|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 5,
    "Neurofibromatosis|_type_1|Tibial_pseudarthrosis": 2,
    "Gastric_cancer|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 265,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder": 3,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neurofibromatosis|_type_1": 4,
    "Neurofibromatosis|_type_1|See_cases|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 5,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_specified|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Myopathy|_centronuclear|_5|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal": 1,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis|_type_1|not_provided|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_specified": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|not_provided": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 2,
    "not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|NF1-related_disorder": 2,
    "Neurofibromatosis|_type_1|not_provided|NF1-related_disorder": 2,
    "not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_specified|not_provided|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 2,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 10,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 2,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis-Noonan_syndrome": 8,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Neurofibromatosis-Noonan_syndrome|not_provided": 1,
    "Neurofibromatosis|_type_1|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 2,
    "not_provided|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder": 5,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "not_provided|not_specified|Neurofibromatosis|_type_1": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Chromosome_17q11.2_deletion_syndrome|_1.4Mb|Neurofibromatosis_type_1_due_to_NF1_mutation_or_intragenic_deletion|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_type_1|NF1-related_disorder": 3,
    "Neurofibromatosis_type_1_due_to_NF1_mutation_or_intragenic_deletion": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided|Atypical_coarctation_of_aorta": 1,
    "not_provided|Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Abnormality_of_the_skin|not_provided|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|not_specified": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|NF1-related_disorder": 3,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 8,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome": 2,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 16,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 2,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Atypical_coarctation_of_aorta|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 21,
    "Neurofibromatosis|_type_1|Malignant_tumor_of_urinary_bladder": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_specified|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 1,
    "Neurofibrmatosis_type_1|Hereditary_cancer-predisposing_syndrome|Abnormality_of_the_skin|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 4,
    "Juvenile_myelomonocytic_leukemia|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder": 5,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|NF1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Gastric_cancer|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 2,
    "not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|RASopathy|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Diffuse_midline_glioma|_H3_K27-altered|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Abnormality_of_the_skin": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|NF1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_provided|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 7,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1": 9,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1": 4,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1|not_provided": 2,
    "Neurofibromatosis|_type_1|Tibial_pseudarthrosis|not_provided|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia": 2,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder": 4,
    "Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 6,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 2,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 6,
    "Malignant_tumor_of_urinary_bladder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Cafe_au_lait_spots|_multiple|not_provided": 1,
    "Optic_nerve_glioma|Cafe_au_lait_spots|_multiple|Neurofibroma|not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Autism_spectrum_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal": 3,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Neurofibroma|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_specified": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|NF1-related_disorder|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_specified|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 6,
    "not_provided|not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|See_cases|not_specified|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_familial_spinal": 3,
    "Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Gastric_cancer|NF1-related_disorder|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Diffuse_intrinsic_pontine_glioma|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibroma|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 3,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer": 1,
    "Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 4,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_specified": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|EEG_with_generalized_slow_activity|Visual_loss|Cafe-au-lait_spot|Abnormality_of_macular_pigmentation|Hyperactivity|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Abnormal_macular_morphology|Strabismus|Abnormality_of_vision|Abnormal_electroretinogram": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Abnormality_of_the_skin": 1,
    "Tibial_pseudarthrosis": 2,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 5,
    "not_specified|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|not_provided|Neurofibromatosis-Noonan_syndrome": 1,
    "Neurofibromatosis|_type_1|Tibial_pseudarthrosis|NF1-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Chromosome_17q11.2_deletion_syndrome|_1.4Mb|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|See_cases|Juvenile_myelomonocytic_leukemia|NF1-related_disorder|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_type_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_specified": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Cardiovascular_phenotype|Hereditary_cancer": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|not_specified|not_provided|Axillary_freckling|Cafe-au-lait_spot|Optic_nerve_glioma|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Tibial_pseudarthrosis|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 3,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|Juvenile_myelomonocytic_leukemia|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder|not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibroma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|NF1-related_disorder|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 2,
    "not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 2,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Neurofibromatosis|_type_1": 7,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 4,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Axillary_freckling|Cafe-au-lait_spot|Neurofibroma|Inguinal_freckling|Cafe_au_lait_spots|_multiple": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|not_specified|not_provided": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia": 7,
    "NF1-related_disorder|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|not_provided": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Cleft_palate": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Gastric_cancer": 1,
    "Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Neurofibroma": 1,
    "See_cases|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 2,
    "NF1-related_disorder|not_specified|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Cafe_au_lait_spots|_multiple": 1,
    "Neurofibromatosis": 3,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Cafe_au_lait_spots|_multiple|Delayed_fine_motor_development|Inguinal_freckling|Large_cafe-au-lait_macules_with_irregular_margins|Lisch_nodules|Axillary_freckling|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|NF1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 2,
    "not_specified|Neurofibromatosis|_type_1|not_provided": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1": 11,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|See_cases": 1,
    "Gastric_cancer|not_specified|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Atypical_coarctation_of_aorta": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder": 1,
    "not_provided|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome": 1,
    "Neurofibromatosis|_familial_spinal|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "not_provided|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 3,
    "Neurofibroma": 2,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|not_specified|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_provided|Neurofibromatosis|_type_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 2,
    "Neurofibromatosis|_type_1|not_specified|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 6,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome": 1,
    "Neurofibromatosis|_type_1|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_specified|Acute_monocytic_leukemia|Acute_monoblastic_leukemia": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|not_specified": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|NF1-related_disorder|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 2,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|NF1-related_disorder": 1,
    "not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Malignant_tumor_of_urinary_bladder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|NF1-related_disorder|Neurofibromatosis|_type_1": 2,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_specified|Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Cafe-au-lait_spot|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 3,
    "not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 2,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia": 4,
    "Neurofibromatosis|_type_1|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|NF1-related_disorder|not_provided": 1,
    "not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Developmental_defect_during_embryogenesis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 2,
    "not_specified|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|RASopathy|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 2,
    "Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 3,
    "NF1-related_disorder|not_provided|Neurofibromatosis|_type_1": 6,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 5,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|Neurofibromatosis|_type_1": 2,
    "not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|not_provided": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 2,
    "not_provided|Neurofibromatosis|_type_1|Abnormality_of_the_skin": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 1,
    "not_provided|RASopathy|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Intellectual_disability": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Astrocytoma_IDH-mutant|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Myeloproliferative_neoplasm|_unclassifiable|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 4,
    "RASopathy|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Cardiovascular_phenotype|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "NF1-related_disorder|Cervical_lymphadenopathy|Abnormal_lymph_node_morphology|Increased_nuchal_translucency|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Focal-onset_seizure|Cafe_au_lait_spots|_multiple|Motor_delay": 1,
    "not_specified|not_provided|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|not_provided|Neurofibromatosis|_type_1|Rhabdomyosarcoma": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia": 5,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 3,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|See_cases": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Lymphedema": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Tuberous_sclerosis_syndrome|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "NF1-related_disorder|Inborn_genetic_diseases|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Inborn_genetic_diseases|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 2,
    "Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_specified|not_provided|Neurofibromatosis|_type_1": 3,
    "not_provided|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Gastric_cancer": 3,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Ovarian_cancer": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis_type_1_due_to_NF1_mutation_or_intragenic_deletion|not_provided|Neurofibromatosis|_type_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1": 2,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1": 3,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 4,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|NF1-related_disorder|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|NF1-related_disorder": 1,
    "not_specified|Juvenile_myelomonocytic_leukemia|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Tibial_pseudarthrosis|Cafe_au_lait_spots|_multiple": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Neurofibroma|Cafe_au_lait_spots|_multiple|Abnormality_of_vision|not_provided": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal": 2,
    "NF1-related_disorder|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Cafe_au_lait_spots|_multiple|Neurofibroma|Optic_nerve_glioma|Axillary_freckling|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Pheochromocytoma": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Neurofibromatosis-Noonan_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_provided|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_type_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "not_provided|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_specified": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "not_specified|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 4,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_specified|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Atypical_coarctation_of_aorta|Optic_nerve_glioma": 1,
    "Gastric_cancer|Neurofibromatosis|_type_1": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Cafe_au_lait_spots|_multiple|Subcutaneous_neurofibroma|Thoracic_scoliosis|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Abnormality_of_the_skin|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Neurofibromatosis|_type_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 2,
    "NF1-related_disorder|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Vascular_dilatation|Neurofibroma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 3,
    "not_provided|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 2,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Juvenile_myelomonocytic_leukemia|not_provided|Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Macrocephaly|Cafe-au-lait_spot|Tibial_pseudarthrosis": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Juvenile_myelomonocytic_leukemia|not_provided": 2,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|not_specified|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 4,
    "OMG-related_disorder|not_provided": 1,
    "OMG-related_disorder": 3,
    "EVI2A-related_disorder|not_provided|See_cases": 1,
    "not_specified|NF1-related_disorder": 2,
    "not_provided|EVI2A-related_disorder": 1,
    "EVI2A-related_disorder": 1,
    "EVI2A-related_disorder|not_specified|not_provided": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Craniopharyngioma|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_specified|not_provided|Neurofibromatosis|_familial_spinal": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Axillary_freckling|Neurofibroma|Cafe_au_lait_spots|_multiple": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|NF1-related_disorder|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|not_provided": 1,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Rhabdomyosarcoma|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Cafe-au-lait_spot|not_provided|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Microcephaly": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|not_provided|Cafe_au_lait_spots|_multiple|Tibial_pseudarthrosis": 1,
    "not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|NF1-related_disorder|Cardiovascular_phenotype|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Juvenile_myelomonocytic_leukemia|Malignant_tumor_of_urinary_bladder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Diffuse_pediatric-type_high-grade_glioma|_H3-wildtype_and_IDH-wildtype|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Atypical_coarctation_of_aorta|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|Retinoblastoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 2,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Rhabdomyosarcoma|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Malignant_tumor_of_urinary_bladder": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Inborn_genetic_diseases": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Tibial_pseudarthrosis|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_type_1": 2,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurodevelopmental_delay|Intellectual_disability": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Rhabdomyosarcoma|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_specified|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Neurofibromatosis|_type_1|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibroma|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|Axillary_freckling|Plexiform_neurofibroma|Cafe-au-lait_spot|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Moyamoya_angiopathy": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurocutaneous_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "NF1-related_disorder|not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Cafe_au_lait_spots|_multiple": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 2,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome": 1,
    "not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Floppy_infant|Cafe_au_lait_spots|_multiple|Delayed_speech_and_language_development|Premature_birth|not_provided|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_specified|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|not_specified": 2,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal": 1,
    "Neurofibromatosis|_type_1|Pilocytic_astrocytoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|Hereditary_cancer|not_specified|not_provided|Neurofibromatosis|_type_1|Intellectual_disability": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Malignant_tumor_of_urinary_bladder|Neurofibromatosis|_type_1": 1,
    "not_provided|Malignant_tumor_of_urinary_bladder|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Cafe_au_lait_spots|_multiple": 1,
    "not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 4,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|not_specified|Juvenile_myelomonocytic_leukemia": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|not_provided": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 3,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "not_specified|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Tibial_pseudarthrosis|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|not_provided|Neurofibromatosis|_familial_spinal": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|not_specified": 3,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_familial_spinal|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 1,
    "not_provided|Cafe-au-lait_spot|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_provided": 1,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome": 1,
    "Rhabdomyosarcoma|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Cafe_au_lait_spots|_multiple|Inguinal_freckling|Neurofibroma|Axillary_freckling|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|not_specified|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Tibial_pseudarthrosis|Neurofibromatosis|_type_1|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Bardet-Biedl_syndrome_9|Cardiovascular_phenotype|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Neurofibromatosis|_type_1|See_cases|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "NF1-related_disorder|Neurofibromatosis|_type_1|Ewing_sarcoma|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis|_type_1|not_provided|Neurofibroma": 1,
    "Astrocytoma_IDH-mutant|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Cafe_au_lait_spots|_multiple|Subcutaneous_neurofibroma": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Precursor_B-cell_acute_lymphoblastic_leukemia|Neurofibromatosis|_type_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_provided": 3,
    "not_specified|NF1-related_disorder|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|NF1-related_disorder|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|Neurofibromatosis|_type_1": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|NF1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibroma|not_provided|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|not_provided": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis|_type_1|Cardiovascular_phenotype|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|NF1-related_disorder": 3,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|Tibial_pseudarthrosis|Rhabdomyosarcoma|not_provided|Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Ewing_sarcoma|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 9,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_1|Cardiovascular_phenotype": 1,
    "Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_urinary_bladder|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Lisch_nodules|Subcutaneous_neurofibroma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_specified|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Chromosome_17q11.2_deletion_syndrome|_1.4Mb|not_specified|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis-Noonan_syndrome|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "Juvenile_myelomonocytic_leukemia|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibroma|not_provided|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal": 1,
    "not_provided|Neurofibromatosis|_type_1|Malignant_tumor_of_urinary_bladder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal": 1,
    "not_specified|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 2,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|not_provided": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|NF1-related_disorder|Abnormality_of_the_skin|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "NF1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 3,
    "NF1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_type_1|NF1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "Neurofibromatosis|_type_1|NF1-related_disorder|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia": 1,
    "NF1-related_disorder|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "NF1-related_disorder|Tibial_pseudarthrosis|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_specified|Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Cardiovascular_phenotype|not_specified|Neurofibromatosis|_type_1": 2,
    "Chromosome_17q11.2_deletion_syndrome|_1.4Mb|not_specified|not_provided|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|See_cases": 1,
    "not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1|NF1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|NF1-related_disorder|not_specified|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia": 1,
    "not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Hereditary_cancer-predisposing_syndrome|not_specified|NF1-related_disorder|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|NF1-related_disorder|not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|NF1-related_disorder|Neurofibromatosis|_type_1|not_specified|not_provided": 1,
    "Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_type_1|Neoplasm_of_brain": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Neurofibromatosis|_type_1|NF1-related_disorder|not_specified|not_provided": 1,
    "Juvenile_myelomonocytic_leukemia|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_1": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_1|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Juvenile_myelomonocytic_leukemia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_type_1|not_provided": 1,
    "Neurofibromatosis|_type_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Neurofibromatosis|_type_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Juvenile_myelomonocytic_leukemia|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis": 1,
    "not_provided|Neurofibromatosis|_type_1|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Juvenile_myelomonocytic_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_familial_spinal": 1,
    "not_specified|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_familial_spinal|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided|Neurofibromatosis|_type_1": 1,
    "not_provided|Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 1,
    "Neurofibromatosis|_familial_spinal|not_provided|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1|Neurofibromatosis-Noonan_syndrome": 4,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_type_1": 11,
    "Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|Neurofibromatosis|_familial_spinal|not_provided": 1,
    "Neurofibromatosis|_familial_spinal|Neurofibromatosis-Noonan_syndrome|Neurofibromatosis|_type_1|Caf\u00e9-au-lait_macules_with_pulmonary_stenosis|not_provided": 1,
    "Inborn_genetic_diseases|Imagawa-Matsumoto_syndrome": 1,
    "Imagawa-Matsumoto_syndrome": 18,
    "not_specified|Imagawa-Matsumoto_syndrome|not_provided": 1,
    "Imagawa-Matsumoto_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Imagawa-Matsumoto_syndrome": 1,
    "Inborn_genetic_diseases|SUZ12-related_disorder": 1,
    "SUZ12-related_disorder": 3,
    "not_provided|Acute_megakaryoblastic_leukemia_in_down_syndrome": 1,
    "SUZ12-related_disorder|not_provided": 2,
    "Non-immune_hydrops_fetalis|Imagawa-Matsumoto_syndrome": 1,
    "not_provided|Imagawa-Matsumoto_syndrome|SUZ12-related_disorder": 1,
    "Imagawa-Matsumoto_syndrome|Weaver_syndrome": 1,
    "not_provided|Imagawa-Matsumoto_syndrome": 1,
    "not_provided|SUZ12-related_disorder": 1,
    "PSMD11-Related_Disorders": 1,
    "PSMD11-associated_obesity_and_neurodevelopmental_disorder": 1,
    "CDK5R1-related_disorder": 1,
    "TMEM98-related_disorder": 3,
    "Nanophthalmos_4": 3,
    "Mitochondrial_DNA_depletion_syndrome_20_(mngie_type)": 13,
    "CCL2-related_disorder|Spina_bifida|_susceptibility_to": 1,
    "CCL2-related_disorder": 2,
    "CCL11-related_disorder": 2,
    "not_provided|Hearing_loss|_autosomal_recessive_99": 1,
    "Hearing_loss|_autosomal_recessive_99|not_provided": 1,
    "TMEM132E-related_disorder|not_provided": 9,
    "TMEM132E-related_disorder": 11,
    "Hearing_loss|_autosomal_recessive_99|not_provided|not_specified": 1,
    "Hearing_loss|_autosomal_recessive_99": 5,
    "not_provided|TMEM132E-related_disorder": 3,
    "Hearing_loss|_autosomal_recessive_99|not_specified|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_99|TMEM132E-related_disorder": 1,
    "not_specified|Hearing_loss|_autosomal_recessive_99": 1,
    "TMEM132E-related_disorder|not_provided|not_specified": 1,
    "not_provided|TMEM132E-related_disorder|not_specified": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_20_(mngie_type)": 2,
    "LIG3-related_disorder|Inborn_genetic_diseases": 1,
    "Mitochondrial_DNA_depletion_syndrome_20_(mngie_type)|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|LIG3-related_disorder": 1,
    "LIG3-related_disorder": 1,
    "Breast_and_Ovarian_Cancer_Susceptibility": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 4,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 275,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 233,
    "not_provided|Hereditary_cancer-predisposing_syndrome|RAD51D-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided": 21,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 27,
    "Hereditary_cancer-predisposing_syndrome|RAD51D-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 20,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 25,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Familial_ovarian_cancer": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "RAD51D-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 8,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 8,
    "Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Hereditary_cancer|RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided": 1,
    "Childhood_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 7,
    "Hereditary_site-specific_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 2,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 10,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 5,
    "RAD51D-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Inherited_ovarian_cancer_(without_breast_cancer)|Gastric_cancer|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 10,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 3,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 24,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|RAD51D-related_disorder|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 14,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer": 1,
    "Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|RAD51D-related_disorder": 1,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Familial_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "RAD51D-related_disorder|Hereditary_site-specific_ovarian_cancer_syndrome|Cancer_or_benign_tumor|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "RAD51D-related_disorder|Malignant_tumor_of_breast|Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified": 11,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|RAD51D-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_carcinoma|Breast_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Familial_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|Hereditary_cancer-predisposing_syndrome|RAD51D-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_provided": 1,
    "Hereditary_cancer|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 2,
    "Diffuse_midline_glioma|_H3_K27-altered|Gastric_cancer|Colorectal_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 4,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "RAD51D-related_disorder|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Familial_ovarian_cancer": 1,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "Familial_ovarian_cancer|RAD51D-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "Deleterious_RAD51D_Gene_Mutation": 2,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast_cancer|_susceptibility_to": 1,
    "RAD51D-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "Breast_and/or_ovarian_cancer|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|not_provided|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Lynch_syndrome_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|RAD51D-related_disorder|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "See_cases|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_disorder": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 2,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Familial_ovarian_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Familial_ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_disorder": 1,
    "RAD51D-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer": 4,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_provided|Ovarian_neoplasm|Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "RAD51D-related_disorder": 4,
    "RAD51D-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 2,
    "RAD51D-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 1,
    "not_specified|Gastric_cancer": 1,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|RAD51D-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast_and/or_ovarian_cancer": 2,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|RAD51D-related_disorder": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Deleterious_RAD51D_Gene_Mutation": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified": 1,
    "RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_provided|RAD51D-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|Hereditary_cancer": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "RAD51D-related_disorder|RAD51D-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|RAD51D-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|RAD51D-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Familial_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "Malignant_tumor_of_breast|not_specified|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Familial_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|RAD51D-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "Ovarian_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_4": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_provided": 1,
    "RAD51D-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "RAD51D-related_cancer_predisposition|RAD51D-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Myofibrillar_myopathy_11": 5,
    "UNC45B-related_disorder": 10,
    "Myofibrillar_myopathy_11|Cataract_43": 5,
    "UNC45B-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|UNC45B-related_disorder": 4,
    "UNC45B-related_disorder|not_specified|not_provided": 1,
    "Myofibrillar_myopathy_11|not_provided|Cataract_43": 1,
    "UNC45B-related_disorder|not_provided": 6,
    "Inborn_genetic_diseases|UNC45B-related_disorder": 2,
    "Myofibrillar_myopathy_11|Inborn_genetic_diseases": 1,
    "Cataract_43": 2,
    "not_provided|UNC45B-related_disorder|Myopathy|Myofibrillar_myopathy_11": 1,
    "not_provided|Myofibrillar_myopathy_11": 1,
    "UNC45B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Platelet-type_bleeding_disorder_20|not_provided": 6,
    "SLFN14-related_disorder|not_provided": 2,
    "Platelet-type_bleeding_disorder_20": 18,
    "SLFN14-related_disorder": 11,
    "not_provided|SLFN14-related_disorder": 2,
    "Inborn_genetic_diseases|Platelet-type_bleeding_disorder_20": 3,
    "Inborn_genetic_diseases|SLFN14-related_disorder": 2,
    "not_provided|Platelet-type_bleeding_disorder_20": 2,
    "SLFN14-related_disorder|not_provided|Platelet-type_bleeding_disorder_20": 1,
    "SLFN14-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Thrombocytopenia|Abnormal_bleeding|Platelet-type_bleeding_disorder_20": 1,
    "Abnormal_bleeding|Thrombocytopenia|Platelet-type_bleeding_disorder_20": 1,
    "Platelet-type_bleeding_disorder_20|Inborn_genetic_diseases": 1,
    "Platelet-type_bleeding_disorder_20|not_provided|SLFN14-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)": 363,
    "not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 15,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B": 28,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 10,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|PEX12-related_disorder": 6,
    "not_provided|Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "PEX12-related_disorder": 4,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Inborn_genetic_diseases": 7,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder": 2,
    "Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 12,
    "Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)|not_provided|Peroxisomal_biogenesis_disorder_3b|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|Peroxisomal_biogenesis_disorder_3b": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "PEX12-related_disorder|not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B": 1,
    "PEX12-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder|not_provided|Peroxisome_biogenesis_disorder_type_3B": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_3A_(Zellweger)|PEX12-related_disorder|Peroxisome_biogenesis_disorder_type_3B": 1,
    "Peroxisome_biogenesis_disorder_type_3B|PEX12-related_disorder|not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "not_specified|not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "PEX12-related_disorder|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "not_provided|PEX12-related_disorder|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|not_specified": 1,
    "Peroxisome_biogenesis_disorder|PEX12-related_disorder|not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B": 1,
    "not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|PEX12-related_disorder": 1,
    "not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Inborn_genetic_diseases": 1,
    "PEX12-related_disorder|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 4,
    "Peroxisome_biogenesis_disorder_type_3B": 2,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|PEX12-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|Peroxisomal_biogenesis_disorder_3b": 1,
    "Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|PEX12-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|PEX12-related_disorder|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "PEX12-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|not_provided": 1,
    "Peroxisome_biogenesis_disorder_type_3B|not_specified|not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_type_3B|not_provided": 1,
    "not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B": 1,
    "not_provided|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|PEX12-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|not_provided": 5,
    "PEX12-related_disorder|Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)": 1,
    "Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)|not_provided": 2,
    "Peroxisome_biogenesis_disorder_3A_(Zellweger)|Peroxisome_biogenesis_disorder_type_3B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "PEX12-related_disorder|not_specified|Peroxisome_biogenesis_disorder_type_3B|Peroxisome_biogenesis_disorder_3A_(Zellweger)|not_provided": 1,
    "GAS2L2-related_disorder": 23,
    "not_provided|GAS2L2-related_disorder": 3,
    "Ciliary_dyskinesia|_primary|_41": 3,
    "GAS2L2-related_disorder|not_provided": 1,
    "not_specified|GAS2L2-related_disorder|Ciliary_dyskinesia|_primary|_41": 1,
    "not_specified|not_provided|GAS2L2-related_disorder": 1,
    "GAS2L2-related_disorder|not_specified|not_provided": 2,
    "Ciliary_dyskinesia|_primary|_41|not_specified": 2,
    "not_specified|GAS2L2-related_disorder": 1,
    "GAS2L2-related_disorder|Ciliary_dyskinesia|_primary|_41|Primary_ciliary_dyskinesia": 1,
    "GAS2L2-related_disorder|not_specified": 1,
    "TAF15-related_disorder": 39,
    "not_provided|TAF15-related_disorder": 18,
    "TAF15-related_disorder|not_specified": 1,
    "TAF15-related_disorder|not_provided": 21,
    "not_specified|TAF15-related_disorder": 4,
    "Human_immunodeficiency_virus_type_1|_rapid_disease_progression_with_infection_by": 1,
    "CCL5-related_condition|Human_immunodeficiency_virus_type_1|_delayed_disease_progression_with_infection_by": 1,
    "PEHO_syndrome": 3,
    "ZNHIT3-related_disorder|not_provided|PEHO_syndrome": 1,
    "ZNHIT3-related_disorder": 2,
    "Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_5": 19,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_5": 226,
    "not_provided|Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_5": 1,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_5": 6,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_5|not_provided": 7,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_5|Inborn_genetic_diseases": 12,
    "not_specified|Hyperphosphatasia_with_intellectual_disability_syndrome_5": 1,
    "not_specified|Inborn_genetic_diseases|Cleft_palate|Abnormal_skeletal_morphology|Global_developmental_delay|not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_5": 1,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_5|not_specified": 1,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_5|Inborn_genetic_diseases": 1,
    "PIGW-related_disorder|Hyperphosphatasia_with_intellectual_disability_syndrome_5|not_provided": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_5|PIGW-related_disorder": 1,
    "GGNBP2-related_disorder": 4,
    "LHX1-related_disorder": 10,
    "ACACA-related_disorder|not_provided": 10,
    "Acetyl-CoA:_carboxylase_deficiency|not_provided": 2,
    "Acetyl-CoA:_carboxylase_deficiency": 4,
    "not_provided|Acetyl-CoA:_carboxylase_deficiency": 1,
    "not_provided|ACACA-related_disorder|not_specified": 1,
    "not_provided|ACACA-related_disorder": 17,
    "ACACA-related_disorder": 8,
    "Acetyl-CoA:_carboxylase_deficiency|not_provided|ACACA-related_disorder": 1,
    "SYNRG-related_disorder": 16,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome": 36,
    "not_provided|Renal_cysts_and_diabetes_syndrome": 17,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|not_provided": 3,
    "Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_specified|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "HNF1B-related_disorder|Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 2,
    "HNF1B-related_disorder": 28,
    "Monogenic_diabetes|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus": 1,
    "not_provided|not_specified|HNF1B-related_disorder": 2,
    "not_provided|HNF1B-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 4,
    "Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|not_provided|HNF1B-related_disorder|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 8,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|not_specified": 2,
    "Renal_cysts_and_diabetes_syndrome|not_provided": 14,
    "not_provided|HNF1B-related_disorder": 6,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|HNF1B-related_disorder": 2,
    "HNF1B-related_disorder|not_specified|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|not_provided": 1,
    "HNF1B-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus": 37,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|HNF1B-related_disorder": 1,
    "HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome": 3,
    "Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|not_specified|not_provided": 2,
    "not_specified|not_provided|HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus": 1,
    "not_provided|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 5,
    "not_specified|Renal_cysts_and_diabetes_syndrome": 1,
    "Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|not_provided": 2,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Nonpapillary_renal_cell_carcinoma|not_specified|HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome": 1,
    "Ovarian_cancer|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus": 1,
    "not_provided|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|Monogenic_diabetes|not_provided": 1,
    "HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|not_provided": 1,
    "Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young": 10,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|not_provided|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma": 1,
    "HNF1B-related_disorder|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF1B-related_disorder|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|not_provided": 1,
    "not_provided|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young": 1,
    "HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|not_provided": 5,
    "Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 1,
    "HNF1B-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF1B-related_disorder|not_provided": 5,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Renal_cysts_and_diabetes_syndrome|not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "not_provided|Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus": 3,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|HNF1B-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|not_specified|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_specified|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 1,
    "HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus": 1,
    "Renal_cysts_and_diabetes_syndrome|Autosomal_dominant_polycystic_liver_disease": 1,
    "Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus": 2,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_provided": 2,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|Hyperechogenic_kidneys": 1,
    "not_provided|Renal_cysts_and_diabetes_syndrome|HNF1B-related_disorder": 1,
    "Autosomal_dominant_medullary_cystic_kidney_disease_with_or_without_hyperuricemia|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF1B-related_disorder|not_provided|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Autosomal_dominant_polycystic_liver_disease|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma": 1,
    "not_provided|not_specified|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|HNF1B-related_disorder": 1,
    "not_provided|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus": 1,
    "Renal_cysts_and_diabetes_syndrome|not_provided|HNF1B-related_disorder": 2,
    "not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|HNF1B-related_disorder|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|not_specified": 1,
    "not_specified|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus": 4,
    "Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_specified|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_provided": 1,
    "not_specified|not_provided|Renal_cysts_and_diabetes_syndrome|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus": 1,
    "Renal_cysts_and_diabetes_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hyperechogenic_kidneys|Renal_cysts_and_diabetes_syndrome": 1,
    "HNF1B-related_disorder|not_provided|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Renal_cysts_and_diabetes_syndrome|See_cases|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|not_provided": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 1,
    "not_provided|Hyperechogenic_kidneys": 1,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF1B-related_disorder|Renal_cysts_and_diabetes_syndrome|not_provided": 1,
    "Hyperuricemic_nephropathy|_familial_juvenile_type_3|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|not_provided|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "HNF1B-related_disorder|not_provided|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_provided|HNF1B-related_disorder": 2,
    "HNF1B-related_disorder|not_specified|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|HNF1B-related_disorder|Monogenic_diabetes": 1,
    "HNF1B-related_disorder|Autosomal_dominant_polycystic_liver_disease|Monogenic_diabetes|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperuricemic_nephropathy|_familial_juvenile_type_3|Renal_cysts_and_diabetes_syndrome": 1,
    "not_provided|Nonpapillary_renal_cell_carcinoma|HNF1B-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract|Renal_cysts_and_diabetes_syndrome|not_specified": 1,
    "HNF1B-related_disorder|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Autosomal_dominant_polycystic_liver_disease|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|not_specified|not_provided": 1,
    "Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|Nonpapillary_renal_cell_carcinoma|not_specified|not_provided": 1,
    "Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome": 1,
    "Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|Renal_cysts_and_diabetes_syndrome|not_provided|not_specified": 1,
    "Nonpapillary_renal_cell_carcinoma|Renal_cysts_and_diabetes_syndrome|Type_2_diabetes_mellitus|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Renal_cysts_and_diabetes_syndrome|Chromophobe_renal_cell_carcinoma": 1,
    "HNF1B-related_disorder|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "HNF1B-related_disorder|Nonpapillary_renal_cell_carcinoma|Type_2_diabetes_mellitus|Renal_cysts_and_diabetes_syndrome|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Nonpapillary_renal_cell_carcinoma|Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Renal_cysts_and_diabetes_syndrome": 1,
    "Congenital_stationary_night_blindness_1E": 55,
    "not_provided|Congenital_stationary_night_blindness_1E": 49,
    "not_provided|GPR179-related_disorder": 7,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1E": 4,
    "not_provided|GPR179-related_disorder|Congenital_stationary_night_blindness_1E": 4,
    "not_provided|Congenital_stationary_night_blindness_1E|not_specified": 4,
    "not_provided|Congenital_stationary_night_blindness_1E|Inborn_genetic_diseases": 6,
    "not_provided|Retinal_dystrophy|Congenital_stationary_night_blindness_1E": 2,
    "not_provided|not_specified|Retinal_dystrophy|Retinitis_pigmentosa|Congenital_stationary_night_blindness_1E": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_stationary_night_blindness_1E": 12,
    "GPR179-related_disorder|not_provided|Congenital_stationary_night_blindness_1E": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_stationary_night_blindness_1E": 6,
    "Congenital_stationary_night_blindness_1E|not_provided": 35,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_1E": 2,
    "not_specified|Congenital_stationary_night_blindness_1E|not_provided": 2,
    "GPR179-related_disorder": 3,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1E|GPR179-related_disorder": 1,
    "GPR179-related_disorder|not_provided": 7,
    "GPR179-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_stationary_night_blindness_1E|Optic_atrophy": 1,
    "not_specified|Congenital_stationary_night_blindness_1E|not_provided|GPR179-related_disorder": 1,
    "Congenital_stationary_night_blindness_1E|not_provided|GPR179-related_disorder": 1,
    "not_provided|Congenital_stationary_night_blindness_1E|GPR179-related_disorder": 2,
    "Congenital_stationary_night_blindness_1E|GPR179-related_disorder|not_provided": 5,
    "not_provided|not_specified|Congenital_stationary_night_blindness_1E": 1,
    "not_provided|GPR179-related_disorder|Congenital_stationary_night_blindness_1E|not_specified": 1,
    "GPR179-related_disorder|Congenital_stationary_night_blindness_1E|not_provided": 2,
    "Congenital_Stationary_Night_Blindness|_Recessive|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_stationary_night_blindness_1E|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|GPR179-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_1E|not_provided": 3,
    "Congenital_stationary_night_blindness|Optic_atrophy|Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_1E": 1,
    "Congenital_stationary_night_blindness_1E|not_specified|not_provided": 1,
    "GPR179-related_disorder|Congenital_stationary_night_blindness_1E|not_provided|not_specified": 1,
    "PCGF2-related_disorder": 4,
    "Turnpenny-fry_syndrome|Wolfram_syndrome_2": 1,
    "not_provided|Inborn_genetic_diseases|PCGF2-related_disorder": 2,
    "PCGF2-related_disorder|not_provided": 5,
    "Turnpenny-fry_syndrome": 3,
    "not_provided|Turnpenny-fry_syndrome": 2,
    "not_provided|PCGF2-related_disorder": 3,
    "Turnpenny-fry_syndrome|PCGF2-related_disorder|not_provided": 1,
    "PCGF2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Turnpenny-fry_syndrome|Global_developmental_delay|Intellectual_disability|Abnormality_of_the_outer_ear|Inborn_genetic_diseases": 1,
    "Turnpenny-fry_syndrome|Inborn_genetic_diseases": 1,
    "PCGF2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "FBXO47-related_disorder": 4,
    "Diamond-Blackfan_anemia|not_provided|RPL19-related_disorder": 2,
    "not_provided|RPL19-related_disorder": 2,
    "RPL19-related_disorder|Diamond-Blackfan_anemia|not_provided": 1,
    "RPL19-related_disorder": 2,
    "MED1-related_condition": 2,
    "not_specified|CDK12-related_disorder": 2,
    "CDK12-related_disorder|not_specified": 8,
    "CDK12-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "not_provided|CDK12-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "CDK12-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|CDK12-related_disorder": 1,
    "CDK12-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "CDK12-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|CDK12-related_disorder|not_provided": 1,
    "CDK12-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "CDK12-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_72": 16,
    "NEUROD2-related_disorder": 3,
    "not_provided|NEUROD2-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_72|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy": 99,
    "Abnormality_of_the_musculature|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25": 32,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 5,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|TCAP-related_disorder|Cardiovascular_phenotype": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Abnormality_of_the_musculature|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25": 11,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy": 15,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Long_QT_syndrome|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 6,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 8,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 2,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Abnormality_of_the_musculature|Elevated_circulating_creatine_kinase_concentration": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_1|Wolff-Parkinson-White_pattern": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy": 5,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 3,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 5,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided": 4,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided": 3,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 5,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 2,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Cardiovascular_phenotype|TCAP-related_disorder": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_specified": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 3,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Cardiovascular_phenotype|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided|Hypertrophic_cardiomyopathy_4": 1,
    "Cardiovascular_phenotype|TCAP-related_disorder|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|TCAP-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|TCAP-related_disorder|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_specified|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Cardiovascular_phenotype": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Primary_dilated_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25|not_specified|Brugada_syndrome|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_specified|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|not_provided": 1,
    "TCAP-related_disorder|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25": 2,
    "not_provided|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_specified|not_provided|Cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ventricular_tachycardia|TCAP-related_disorder|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_25|Primary_familial_hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_25|not_provided|Cardiovascular_phenotype": 1,
    "TCAP-related_disorder": 1,
    "Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_25|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2G|Hypertrophic_cardiomyopathy_25": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_4|not_provided": 6,
    "not_provided|Hyperphosphatasia_with_intellectual_disability_syndrome_4": 7,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_4|Inborn_genetic_diseases|PGAP3-related_disorder|not_provided": 1,
    "PGAP3-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|PGAP3-related_disorder": 1,
    "not_provided|PGAP3-related_disorder": 3,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_4|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Hyperphosphatasia_with_intellectual_disability_syndrome_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hyperphosphatasia_with_intellectual_disability_syndrome_4": 1,
    "not_provided|Gastric_cancer|Glioma_susceptibility_1|Ovarian_cancer|Lung_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive": 2,
    "not_provided|Glioma_susceptibility_1|Lung_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Gastric_cancer|Ovarian_cancer": 2,
    "not_provided|Glioma_susceptibility_1|Ovarian_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Gastric_cancer|Lung_cancer": 3,
    "not_provided|Glioma_susceptibility_1|Ovarian_cancer|Lung_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Gastric_cancer": 4,
    "Glioma_susceptibility_1|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Ovarian_cancer|Gastric_cancer|Lung_cancer": 12,
    "Gastric_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Lung_cancer|Glioma_susceptibility_1|Ovarian_cancer|not_specified|not_provided": 3,
    "not_provided|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Ovarian_cancer|Lung_cancer|Gastric_cancer|Glioma_susceptibility_1": 1,
    "Glioma_susceptibility_1|Ovarian_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Gastric_cancer|Lung_cancer|not_provided": 2,
    "Visceral_neuropathy|_familial|_2|_autosomal_recessive|not_provided": 2,
    "Visceral_neuropathy|_familial|_2|_autosomal_recessive|Lung_cancer|Glioma_susceptibility_1|Ovarian_cancer|Gastric_cancer|not_specified|not_provided": 1,
    "Lung_cancer|Ovarian_cancer|Gastric_cancer|Glioma_susceptibility_1|Visceral_neuropathy|_familial|_2|_autosomal_recessive|not_provided": 1,
    "not_provided|Ovarian_cancer|Gastric_cancer|Lung_cancer|Glioma_susceptibility_1|Visceral_neuropathy|_familial|_2|_autosomal_recessive": 3,
    "Ovarian_cancer|Lung_cancer|Glioma_susceptibility_1|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Gastric_cancer|not_provided": 1,
    "not_specified|ERBB2_POLYMORPHISM|not_provided": 1,
    "ERBB2_POLYMORPHISM|not_specified|not_provided": 1,
    "Visceral_neuropathy|_familial|_2|_autosomal_recessive": 1,
    "Lung_adenocarcinoma|Non-small_cell_lung_carcinoma": 1,
    "not_specified|Myelodysplastic_syndrome|not_provided": 1,
    "Lung_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Glioma_susceptibility_1|Ovarian_cancer|not_provided": 1,
    "not_provided|Visceral_neuropathy|_familial|_2|_autosomal_recessive": 2,
    "not_provided|Glioma_susceptibility_1|Gastric_cancer|Ovarian_cancer|Visceral_neuropathy|_familial|_2|_autosomal_recessive|Lung_cancer": 1,
    "Neuroepithelial_tumor|_PATZ1_fusion-positive": 1,
    "Immunodeficiency_84": 5,
    "Immunodeficiency_84|not_specified": 1,
    "THRA-related_disorder|Congenital_nongoitrous_hypothyroidism_6|not_provided": 1,
    "THRA-related_disorder": 2,
    "Congenital_nongoitrous_hypothyroidism_6": 13,
    "THRA-related_disorder|not_provided": 1,
    "not_specified|THRA-related_disorder|not_provided": 1,
    "Congenital_nongoitrous_hypothyroidism_6|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_nongoitrous_hypothyroidism_6": 1,
    "Familial_cold_autoinflammatory_syndrome_2": 833,
    "Meier-Gorlin_syndrome_5": 18,
    "not_specified|not_provided|Meier-Gorlin_syndrome_5": 6,
    "not_provided|Meier-Gorlin_syndrome_5": 5,
    "CDC6-related_disorder|not_provided": 1,
    "CDC6-related_disorder|not_specified|not_provided": 1,
    "Meier-Gorlin_syndrome_5|not_provided|CDC6-related_disorder": 1,
    "Meier-Gorlin_syndrome_5|not_specified|not_provided": 1,
    "not_provided|not_specified|Meier-Gorlin_syndrome_5": 1,
    "Meier-Gorlin_syndrome_5|not_provided": 2,
    "Meier-Gorlin_syndrome|not_provided": 1,
    "Tretinoin_response|not_provided": 1,
    "Tretinoin_response": 1,
    "TOP2A-related_disorder": 3,
    "not_provided|TOP2A-related_disorder": 3,
    "TOP2A-related_disorder|not_provided": 4,
    "Dna_topoisomerase_II|_resistance_to_inhibition_of|_by_amsacrine": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis": 1,
    "Familial_meningioma|Coffin-Siris_syndrome_5|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided|Coffin-Siris_syndrome_5": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 6,
    "SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 4,
    "SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|SMARCB1-related_schwannomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|SMARCE1-related_disorder": 1,
    "not_provided|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|SMARCE1-related_disorder|Familial_meningioma": 2,
    "Familial_meningioma|SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis": 1,
    "SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_meningioma": 1,
    "SMARCE1-related_disorder|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided": 8,
    "Familial_meningioma|Coffin-Siris_syndrome_5": 2,
    "not_provided|Familial_meningioma": 4,
    "Familial_meningioma|Coffin-Siris_syndrome_5|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Coffin-Siris_syndrome_5": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Coffin-Siris_syndrome_5|not_provided": 2,
    "Coffin-Siris_syndrome_5|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome_5": 1,
    "not_specified|Familial_meningioma": 2,
    "not_provided|Familial_meningioma|Coffin-Siris_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCE1-related_disorder|Familial_meningioma|Coffin-Siris_syndrome_5|Hereditary_cancer-predisposing_syndrome": 1,
    "Coffin-Siris_syndrome_5": 7,
    "SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_meningioma|not_provided|Coffin-Siris_syndrome_5": 1,
    "Familial_meningioma|Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCE1-related_disorder|Familial_meningioma": 1,
    "Familial_meningioma|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "SMARCE1-related_disorder": 2,
    "not_provided|Familial_meningioma|Coffin-Siris_syndrome_5": 1,
    "not_provided|SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_meningioma|SMARCB1-related_schwannomatosis": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|SMARCE1-related_disorder": 1,
    "Coffin-Siris_syndrome_5|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 2,
    "Familial_meningioma|SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome_5": 1,
    "Coffin-Siris_syndrome_5|Familial_meningioma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_meningioma|Meningioma": 1,
    "Tessier_cleft": 1,
    "Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome_5|Familial_meningioma": 1,
    "SMARCE1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma": 1,
    "Hypotrichosis_8|Wooly_hair|_autosomal_recessive_3": 1,
    "Wooly_hair|_autosomal_recessive_3|not_specified": 1,
    "Wooly_hair|_autosomal_recessive_3|Autosomal_Recessive_Hypotrichosis_with_Woolly_Hair": 1,
    "KRT25-related_disorder|not_provided": 1,
    "not_provided|KRT25-related_disorder": 3,
    "Ichthyosis_hystrix_gravior|Epidermolytic_hyperkeratosis_1|Congenital_reticular_ichthyosiform_erythroderma|Ichthyosis|_annular_epidermolytic_1": 1,
    "not_provided|KRT10-related_disorder": 6,
    "not_specified|not_provided|KRT10-related_disorder|Epidermolytic_ichthyosis|Annular_epidermolytic_ichthyosis|Congenital_reticular_ichthyosiform_erythroderma": 1,
    "not_provided|Congenital_reticular_ichthyosiform_erythroderma|Epidermolytic_ichthyosis|Annular_epidermolytic_ichthyosis|not_specified": 1,
    "Ichthyosis|_annular_epidermolytic_1|Epidermolytic_hyperkeratosis_2A|_autosomal_dominant|Congenital_reticular_ichthyosiform_erythroderma|Ichthyosis_hystrix_gravior|Epidermolytic_hyperkeratosis_2B|_autosomal_recessive": 3,
    "not_provided|Ichthyosis_hystrix_gravior|Epidermolytic_hyperkeratosis_2A|_autosomal_dominant|Congenital_reticular_ichthyosiform_erythroderma|Epidermolytic_hyperkeratosis_2B|_autosomal_recessive|Ichthyosis|_annular_epidermolytic_1|KRT10-related_disorder": 1,
    "KRT10-related_disorder": 15,
    "KRT10-related_disorder|not_provided": 7,
    "not_provided|Congenital_reticular_ichthyosiform_erythroderma": 1,
    "KRT10-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|KRT10-related_disorder": 1,
    "Epidermolytic_ichthyosis|Annular_epidermolytic_ichthyosis|Congenital_reticular_ichthyosiform_erythroderma|not_provided": 1,
    "Congenital_reticular_ichthyosiform_erythroderma|Epidermolytic_hyperkeratosis_2A|_autosomal_dominant": 1,
    "not_provided|Ichthyosis|_annular_epidermolytic_1": 1,
    "not_provided|Epidermolytic_hyperkeratosis_2A|_autosomal_dominant": 5,
    "Epidermolytic_hyperkeratosis_2B|_autosomal_recessive|not_provided": 2,
    "Epidermolytic_hyperkeratosis_2A|_autosomal_dominant|not_provided": 3,
    "Ichthyosis_hystrix_gravior": 1,
    "not_provided|Epidermolytic_hyperkeratosis_2B|_autosomal_recessive": 1,
    "Epidermolytic_hyperkeratosis_2B|_autosomal_recessive": 1,
    "Epidermolytic_hyperkeratosis_1|Epidermolytic_hyperkeratosis_2A|_autosomal_dominant|KRT10-related_disorder|not_provided|Epidermolytic_ichthyosis": 1,
    "Epidermolytic_hyperkeratosis_2A|_autosomal_dominant|Autosomal_dominant_epidermolytic_ichthyosis|KRT10-related_disorder|Epidermolytic_acanthoma|Epidermolytic_nevus|Epidermolytic_ichthyosis|Annular_epidermolytic_ichthyosis|Congenital_reticular_ichthyosiform_erythroderma|not_provided": 1,
    "Congenital_reticular_ichthyosiform_erythroderma|Annular_epidermolytic_ichthyosis|Epidermolytic_ichthyosis|not_provided": 1,
    "not_provided|Annular_epidermolytic_ichthyosis|Congenital_reticular_ichthyosiform_erythroderma|Epidermolytic_ichthyosis|KRT10-related_disorder": 1,
    "KRT12-related_disorder|not_provided": 1,
    "KRT12-related_disorder": 2,
    "not_provided|Corneal_dystrophy|_Meesmann|_1": 7,
    "Corneal_dystrophy|_Meesmann|_1": 6,
    "not_provided|KRT12-related_disorder": 2,
    "not_provided|KRT12-related_disorder|Inborn_genetic_diseases": 1,
    "Corneal_dystrophy|_Meesmann|_1|not_provided": 1,
    "KRT20-related_disorder": 1,
    "Autism_spectrum_disorder|See_cases|not_provided": 1,
    "White_sponge_nevus_2": 29,
    "not_provided|White_sponge_nevus_2": 10,
    "White_sponge_nevus_2|not_provided": 5,
    "KRT13-related_disorder": 4,
    "KRT13-related_disorder|White_sponge_nevus_2": 6,
    "Inborn_genetic_diseases|White_sponge_nevus_2": 1,
    "Inborn_genetic_diseases|White_sponge_nevus_2|not_provided": 1,
    "White_sponge_nevus_2|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|White_sponge_nevus_2": 1,
    "KRT13-related_disorder|not_provided|White_sponge_nevus_2": 3,
    "Inborn_genetic_diseases|not_provided|White_sponge_nevus_2": 1,
    "KRT13-related_disorder|White_sponge_nevus_2|not_provided": 1,
    "Palmoplantar_keratoderma|_epidermolytic": 37,
    "not_provided|Palmoplantar_keratoderma|_epidermolytic": 22,
    "Epidermolytic_palmoplantar_keratoderma|_1": 6,
    "not_provided|KRT9-related_disorder": 1,
    "KRT9-related_disorder|not_provided|Palmoplantar_keratoderma|_epidermolytic": 2,
    "Palmoplantar_keratoderma|_epidermolytic|Inborn_genetic_diseases": 2,
    "Palmoplantar_keratoderma|_epidermolytic|not_provided": 3,
    "KRT9-related_disorder": 6,
    "not_provided|Palmoplantar_keratoderma|_epidermolytic|KRT9-related_disorder": 2,
    "Palmoplantar_keratoderma|_epidermolytic|not_provided|KRT9-related_disorder": 1,
    "not_provided|Epidermolytic_palmoplantar_keratoderma|_1|Palmoplantar_keratoderma|_epidermolytic": 1,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma|_epidermolytic|not_provided": 1,
    "not_provided|Epidermolytic_palmoplantar_keratoderma|_1|Inborn_genetic_diseases": 1,
    "Epidermolytic_palmoplantar_keratoderma|_1|not_provided": 5,
    "not_provided|Epidermolytic_palmoplantar_keratoderma|_1": 6,
    "Epidermolytic_palmoplantar_keratoderma|_1|Inborn_genetic_diseases|not_provided|Palmoplantar_keratoderma|_epidermolytic": 1,
    "Epidermolytic_palmoplantar_keratoderma|_1|Palmoplantar_keratoderma|not_provided|Palmoplantar_keratoderma|_epidermolytic": 1,
    "Epidermolytic_palmoplantar_keratoderma|_1|not_provided|Palmoplantar_keratoderma|_epidermolytic": 2,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma|_epidermolytic": 2,
    "not_provided|Palmoplantar_keratoderma|_epidermolytic|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Palmoplantar_keratoderma|_epidermolytic": 1,
    "Epidermolysis_bullosa_simplex_1C|_localized|not_provided": 3,
    "KRT14-related_disorder": 5,
    "not_provided|Epidermolysis_bullosa_simplex_1A|_generalized_severe": 3,
    "not_provided|Epidermolysis_bullosa_simplex|_Koebner_type": 4,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|Naegeli-Franceschetti-Jadassohn_syndrome|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1C|_localized|KRT14-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa_simplex_1C|_localized": 3,
    "KRT14-related_disorder|not_provided": 4,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|not_provided|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_1C|_localized": 1,
    "Epidermolysis_bullosa_simplex_1C|_localized|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Epidermolysis_bullosa_simplex|_Koebner_type|Naegeli-Franceschetti-Jadassohn_syndrome|not_provided": 1,
    "Palmoplantar_blistering|Skin_fragility_with_non-scarring_blistering|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1A|_generalized_severe": 1,
    "not_provided|Epidermolysis_bullosa_simplex_1C|_localized": 2,
    "not_provided|Epidermolysis_bullosa_simplex|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive": 1,
    "Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive": 2,
    "not_provided|KRT14-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive": 2,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|Naegeli-Franceschetti-Jadassohn_syndrome|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1C|_localized|not_provided": 1,
    "Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|not_provided": 2,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|Epidermolysis_bullosa_simplex_1C|_localized|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|not_provided": 1,
    "Dermatopathia_pigmentosa_reticularis|KRT14-related_disorder|Epidermolysis_bullosa_simplex_1A|_generalized_severe|not_provided": 1,
    "Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1A|_generalized_severe|KRT14-related_disorder|not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa_simplex": 1,
    "Dermatopathia_pigmentosa_reticularis": 2,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|Naegeli-Franceschetti-Jadassohn_syndrome|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1C|_localized|not_specified|not_provided": 2,
    "Epidermolysis_bullosa_simplex_1A|_generalized_severe|not_provided|KRT14-related_disorder": 1,
    "not_provided|Epidermolysis_bullosa_simplex|_Koebner_type|Dermatopathia_pigmentosa_reticularis": 1,
    "not_provided|KRT14-related_disorder|not_specified": 1,
    "not_specified|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Naegeli-Franceschetti-Jadassohn_syndrome|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1C|_localized|not_provided": 1,
    "not_provided|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Dermatopathia_pigmentosa_reticularis|Naegeli-Franceschetti-Jadassohn_syndrome|Epidermolysis_bullosa_simplex_1C|_localized": 1,
    "not_provided|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex_1C|_localized|Naegeli-Franceschetti-Jadassohn_syndrome": 1,
    "Inborn_genetic_diseases|Naegeli-Franceschetti-Jadassohn_syndrome|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive|Epidermolysis_bullosa_simplex|_Koebner_type|Epidermolysis_bullosa_simplex_1A|_generalized_severe|Dermatopathia_pigmentosa_reticularis|Epidermolysis_bullosa_simplex_1C|_localized": 1,
    "not_provided|Sj\u00f6gren-Larsson_syndrome|Abnormality_of_the_skin|Epidermolysis_bullosa_simplex_1D|_generalized|_intermediate_or_severe|_autosomal_recessive": 1,
    "not_provided|Dermatopathia_pigmentosa_reticularis": 1,
    "Naegeli-Franceschetti-Jadassohn_syndrome|not_provided": 1,
    "not_provided|Naegeli-Franceschetti-Jadassohn_syndrome": 1,
    "not_provided|Palmoplantar_keratoderma|_nonepidermolytic|_focal_1": 1,
    "not_provided|Pachyonychia_congenita_1|Palmoplantar_keratoderma|_nonepidermolytic|_focal_1": 3,
    "Palmoplantar_keratoderma|_nonepidermolytic|_focal_1": 2,
    "not_provided|KRT16-related_disorder": 4,
    "Pachyonychia_congenita_1|Palmoplantar_keratoderma|_nonepidermolytic|_focal_1|not_provided": 4,
    "not_specified|Pachyonychia_congenita_1|not_provided": 1,
    "KRT16-related_disorder": 4,
    "Inborn_genetic_diseases|KRT16-related_disorder|not_provided": 1,
    "Pachyonychia_congenita_1|Palmoplantar_keratoderma|_nonepidermolytic|_focal_1": 3,
    "KRT16-related_disorder|not_provided": 4,
    "Pachyonychia_congenita_1|KRT16-related_disorder|not_provided": 1,
    "Palmoplantar_keratoderma|_epidermolytic|not_provided|Pachyonychia_congenita_1": 1,
    "KRT16-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Pachyonychia_congenita_1": 4,
    "Pachyonychia_congenita_1|not_provided": 3,
    "KRT16-related_disorder|Palmoplantar_keratoderma|_nonepidermolytic|_focal_1|Pachyonychia_congenita_1|not_provided": 1,
    "not_provided|Palmoplantar_keratoderma|_nonepidermolytic|_focal_1|Pachyonychia_congenita_1": 2,
    "Pachyonychia_congenita_1": 2,
    "KRT17-related_disorder": 6,
    "Pachyonychia_congenita_2|Steatocystoma_multiplex": 2,
    "Anonychia": 12,
    "KRT17-related_disorder|Steatocystoma_multiplex|Pachyonychia_congenita_2|not_provided": 1,
    "Pachyonychia_congenita_2|Steatocystoma_multiplex|not_provided": 3,
    "KRT17-related_disorder|not_provided": 4,
    "not_provided|KRT17-related_disorder": 3,
    "Steatocystoma_multiplex": 2,
    "Pachyonychia_congenita_2|not_provided": 5,
    "not_provided|Pachyonychia_congenita_2": 4,
    "not_provided|Pachyonychia_congenita_2|Steatocystoma_multiplex": 1,
    "Pachyonychia_congenita_2|Steatocystoma_multiplex|not_provided|Abnormality_of_the_skin": 1,
    "Steatocystoma_multiplex|not_provided": 1,
    "Pachyonychia_congenita_2": 1,
    "not_specified|KRT17-related_disorder|not_provided": 1,
    "HAP1-related_disorder": 18,
    "HAP1-related_disorder|not_provided": 2,
    "not_provided|HAP1-related_disorder": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 349,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 6,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 189,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 14,
    "Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Naxos_disease": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|not_specified": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 7,
    "Cardiomyopathy|Naxos_disease|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 67,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype": 50,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 44,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 3,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiovascular_phenotype": 13,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 55,
    "not_provided|Cardiovascular_phenotype|JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Cardiovascular_phenotype|JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype|not_provided": 6,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|JUP-related_disorder|not_specified|Cardiomyopathy": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "JUP-related_disorder|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 5,
    "JUP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|not_provided": 5,
    "not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified": 12,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|JUP-related_disorder": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|Cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy|Hypertrophic_cardiomyopathy|JUP-related_disorder|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided": 9,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified": 3,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "Cardiovascular_phenotype|JUP-related_disorder|not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 6,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided": 7,
    "not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 4,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|JUP-related_disorder": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|JUP-related_disorder|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 11,
    "Hypertrophic_cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided": 1,
    "JUP-related_disorder|not_provided|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy": 1,
    "not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|not_specified": 4,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified": 5,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided": 10,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided": 2,
    "Primary_dilated_cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype|not_specified|JUP-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided": 2,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|not_specified": 2,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|Naxos_disease": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12": 3,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided": 5,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 4,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|Cardiovascular_phenotype|not_provided": 3,
    "Naxos_disease": 7,
    "not_provided|Ventricular_fibrillation|_paroxysmal_familial|_type_1|JUP-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|Cardiomyopathy": 1,
    "not_provided|Naxos_disease|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|not_provided": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|Cardiomyopathy": 1,
    "Cardiac_arrhythmia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Cardiomyopathy": 1,
    "not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|Cardiovascular_phenotype": 6,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|JUP-related_disorder": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|Cardiovascular_phenotype": 3,
    "not_provided|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|Naxos_disease": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Naxos_disease|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Cardiovascular_phenotype": 4,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "not_provided|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiomyopathy|not_specified": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|Left_ventricular_noncompaction|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified": 2,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|JUP-related_disorder": 2,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|JUP-related_disorder|not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "JUP-related_disorder|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype": 1,
    "JUP-related_disorder|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "Cardiomyopathy|JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Naxos_disease|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|JUP-related_disorder|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "Palmoplantar_keratodermas": 1,
    "not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiomyopathy|not_provided": 1,
    "Cardiac_arrhythmia|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|not_provided": 1,
    "not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiovascular_phenotype|Naxos_disease|not_specified": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|not_specified": 1,
    "JUP-related_disorder|Cardiovascular_phenotype|not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "JUP-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|not_provided|Cardiomyopathy": 1,
    "Wolff-Parkinson-White_pattern|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype": 1,
    "JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiovascular_phenotype": 1,
    "JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "JUP-related_disorder": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|not_provided": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiomyopathy": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|JUP-related_disorder|not_specified": 2,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Cardiomyopathy": 1,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|Left_ventricular_noncompaction_1": 1,
    "Naxos_disease|non-syndromic_arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "JUP-related_disorder|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|Wolff-Parkinson-White_pattern|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided": 1,
    "JUP-related_disorder|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|not_specified|not_provided": 4,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|JUP-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_dilated_cardiomyopathy|Cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Primary_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|JUP-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "Cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Cardiovascular_phenotype|not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Conduction_disorder_of_the_heart|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Long_QT_syndrome": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Left_ventricular_hypertrophy|Cardiovascular_phenotype|not_provided|not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiomyopathy": 1,
    "not_provided|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Wolff-Parkinson-White_pattern|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|not_specified|Cardiomyopathy": 1,
    "not_specified|JUP-related_disorder|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|Cardiomyopathy": 1,
    "JUP-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Naxos_disease|JUP-related_disorder|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_12|Cardiovascular_phenotype|Naxos_disease|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Naxos_disease|Arrhythmogenic_right_ventricular_dysplasia_12|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_11": 40,
    "Osteogenesis_imperfecta_type_11|not_provided": 18,
    "not_provided|Osteogenesis_imperfecta_type_11": 13,
    "FKBP10-related_disorder|not_provided": 6,
    "Bruck_syndrome_1": 3,
    "not_provided|FKBP10-related_disorder": 3,
    "FKBP10-related_disorder|not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_11": 2,
    "Osteogenesis_imperfecta_type_11|Inborn_genetic_diseases": 3,
    "Bruck_syndrome_1|Osteogenesis_imperfecta_type_11|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Bruck_syndrome_1|Osteogenesis_imperfecta": 1,
    "FKBP10-related_disorder": 2,
    "Bruck_syndrome|not_provided": 1,
    "Osteogenesis_imperfecta_type_11|not_provided|FKBP10-related_disorder|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_11|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|FKBP10-related_disorder": 1,
    "Osteogenesis_imperfecta_type_11|not_specified|not_provided": 1,
    "Bruck_syndrome_1|Inborn_genetic_diseases|Osteogenesis_imperfecta_type_11|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_11|not_specified": 2,
    "Inborn_genetic_diseases|FKBP10-related_disorder|not_provided": 1,
    "Bruck_syndrome_1|Osteogenesis_imperfecta_type_11": 6,
    "not_provided|Bruck_syndrome_1|Osteogenesis_imperfecta_type_11": 1,
    "Bruck_syndrome_1|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_11": 1,
    "Osteogenesis_imperfecta_type_12|Osteogenesis_imperfecta_type_11|Bruck_syndrome_1|Abnormality_of_the_skeletal_system|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Osteogenesis_imperfecta_type_11|Bruck_syndrome_1": 1,
    "Osteogenesis_imperfecta|Inborn_genetic_diseases|not_provided|FKBP10-related_disorder|not_specified": 1,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_11|Osteogenesis_imperfecta": 1,
    "Bruck_syndrome_1|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_11|Bruck_syndrome_1": 1,
    "FKBP10-related_disorder|not_provided|Osteogenesis_imperfecta_type_11": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_11|Osteogenesis_imperfecta": 1,
    "Bruck_syndrome_1|Osteogenesis_imperfecta_type_11|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|FKBP10-related_disorder|Osteogenesis_imperfecta_type_11": 1,
    "Bruck_syndrome_1|FKBP10-related_disorder": 1,
    "FKBP10-related_disorder|Osteogenesis_imperfecta|not_provided": 1,
    "Bruck_syndrome_1|not_provided": 2,
    "not_specified|not_provided|FKBP10-related_disorder|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|Bruck_syndrome_1": 1,
    "Bruck_syndrome_1|Osteogenesis_imperfecta_type_11|not_provided|Osteogenesis_imperfecta|not_specified|Osteogenesis_Imperfecta|_Recessive": 1,
    "not_provided|Bruck_syndrome_1|FKBP10-related_disorder": 1,
    "Osteogenesis_imperfecta_type_11|not_provided|Bruck_syndrome_1": 1,
    "Bruck_syndrome_1|Osteogenesis_imperfecta_type_11|not_provided": 3,
    "Osteogenesis_imperfecta_type_12|Bruck_syndrome_1": 1,
    "not_specified|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_11": 1,
    "FKBP10-related_disorder|Osteogenesis_imperfecta_type_11|not_provided": 1,
    "Osteogenesis_imperfecta_type_11|FKBP10-related_disorder|not_provided": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_11": 1,
    "Inborn_genetic_diseases|Bruck_syndrome_1|Osteogenesis_imperfecta_type_11|not_provided": 1,
    "Osteogenesis_imperfecta|FKBP10-related_disorder|not_provided": 1,
    "KLHL10-related_disorder|Non-obstructive_azoospermia": 1,
    "Spermatogenic_failure_11|not_provided": 3,
    "not_provided|Spermatogenic_failure_11": 1,
    "Non-obstructive_azoospermia|KLHL10-related_disorder|not_provided": 1,
    "Spermatogenic_failure_11": 3,
    "KLHL10-related_disorder": 2,
    "Primary_ciliary_dyskinesia_35": 7,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_35": 2,
    "ODAD4-related_disorder": 9,
    "Myopia_2|_autosomal_dominant": 5,
    "Leukodystrophy|_hypomyelinating|_20": 3,
    "CNP-related_disorder": 1,
    "not_provided|CNP-related_disorder": 1,
    "not_specified|Myopia_2|_autosomal_dominant": 1,
    "DNAJC7-related_condition": 1,
    "DHX58-associated_Neurodevelopmental_disorder": 1,
    "RAB5C-associated_macrocephaly_and_developmental_delay": 1,
    "RAB5C-related_disorder|Inborn_genetic_diseases": 1,
    "Macrocephaly-developmental_delay_syndrome": 87,
    "RAB5C-related_neurodevelopmental_disorder": 1,
    "HCRT-related_disorder": 4,
    "Narcolepsy_1": 1,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 381,
    "Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 5,
    "Inborn_genetic_diseases|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 15,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant": 4,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_provided": 9,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|STAT5B-related_disorder": 2,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Inborn_genetic_diseases": 7,
    "not_provided|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 10,
    "not_specified|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|not_provided": 1,
    "not_provided|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_specified": 4,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|not_specified|not_provided": 1,
    "STAT5B-related_disorder|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 2,
    "Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant": 3,
    "STAT5B-related_disorder": 4,
    "not_specified|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 5,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|not_provided|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 1,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|STAT5B-related_disorder|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 1,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_provided|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|not_specified": 1,
    "not_specified|not_provided|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive": 1,
    "STAT5B-related_growth_hormone_insensitivity_syndrome": 1,
    "Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant|not_provided": 2,
    "Growth_hormone_insensitivity_syndrome_with_immune_dysregulation|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Short_stature": 1,
    "not_specified|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_provided": 1,
    "not_provided|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_specified": 1,
    "not_provided|Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|Growth_hormone_insensitivity_syndrome_with_immune_dysregulation_2|_autosomal_dominant": 1,
    "Growth_hormone_insensitivity_with_immune_dysregulation_1|_autosomal_recessive|not_specified|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 68,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_provided": 4,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 5,
    "not_provided|Hyper-IgE_syndrome": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_provided": 19,
    "Inborn_genetic_diseases|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 1,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 194,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 281,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|Inborn_genetic_diseases": 2,
    "not_specified|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_specified": 9,
    "STAT3-related_early-onset_multisystem_autoimmune_disease": 14,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_specified|STAT3-related_disorder|STAT3-related_early-onset_multisystem_autoimmune_disease|not_provided": 1,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 6,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_disorder": 3,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_early-onset_multisystem_autoimmune_disease|not_provided": 2,
    "not_specified|not_provided|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 2,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_provided": 9,
    "Inborn_genetic_diseases|STAT3-related_early-onset_multisystem_autoimmune_disease|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|Inherited_Immunodeficiency_Diseases|not_provided|STAT3-related_disorder|STAT3_gain_of_function": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|Inherited_Immunodeficiency_Diseases": 2,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_provided|not_specified": 2,
    "STAT3-related_disorder|not_provided|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_specified": 1,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_early-onset_multisystem_autoimmune_disease|not_specified": 1,
    "not_provided|STAT3-related_early-onset_multisystem_autoimmune_disease": 2,
    "EBV-positive_nodal_T-_and_NK-cell_lymphoma|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_specified": 1,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|Hyper-IgE_syndrome": 2,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_provided": 1,
    "not_specified|EBV-positive_nodal_T-_and_NK-cell_lymphoma|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_provided|Malignant_lymphoma|_large_B-cell|_diffuse": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_early-onset_multisystem_autoimmune_disease|STAT3_gain_of_function": 1,
    "See_cases|EBV-Positive_Inflammatory_Follicular_Dendritic_Cell_Sarcoma|not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 1,
    "STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|not_specified": 5,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|STAT3-related_early-onset_multisystem_autoimmune_disease": 1,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|STAT3-related_early-onset_multisystem_autoimmune_disease": 1,
    "STAT3-related_disorder": 5,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|STAT3-related_disorder|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_early-onset_multisystem_autoimmune_disease|STAT3_gain_of_function|Hyper-IgE_syndrome|not_provided|not_specified": 1,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 7,
    "STAT3-related_disorder|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_provided|not_specified": 1,
    "STAT3-related_disorder|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|Inborn_genetic_diseases": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_specified|not_provided": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|STAT3-related_disorder": 3,
    "not_specified|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 2,
    "STAT3-related_early-onset_multisystem_autoimmune_disease|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 2,
    "not_provided|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_disorder|STAT3-related_early-onset_multisystem_autoimmune_disease": 1,
    "STAT3-related_early-onset_multisystem_autoimmune_disease|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 2,
    "not_provided|not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_early-onset_multisystem_autoimmune_disease": 1,
    "STAT3-related_early-onset_multisystem_autoimmune_disease|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 2,
    "Inherited_Immunodeficiency_Diseases|not_provided|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 1,
    "STAT3-related_early-onset_multisystem_autoimmune_disease|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_provided": 1,
    "STAT3-related_disorder|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|Inborn_genetic_diseases": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|STAT3-related_early-onset_multisystem_autoimmune_disease|Inherited_Immunodeficiency_Diseases": 1,
    "not_provided|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 3,
    "not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_disorder|STAT3_gain_of_function": 1,
    "STAT3-related_disorder|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant": 2,
    "STAT3-related_disorder|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_provided": 1,
    "not_provided|STAT3_gain_of_function|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "STAT3-related_disorder|not_specified|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function": 1,
    "not_provided|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3_gain_of_function|not_specified|STAT3-related_early-onset_multisystem_autoimmune_disease": 1,
    "Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|STAT3-related_early-onset_multisystem_autoimmune_disease": 1,
    "not_provided|STAT3-related_disorder": 1,
    "Congenital_generalized_lipodystrophy_type_4": 53,
    "not_provided|Congenital_generalized_lipodystrophy_type_4": 16,
    "Congenital_generalized_lipodystrophy_type_4|not_provided": 3,
    "not_provided|CAVIN1-related_disorder|Congenital_generalized_lipodystrophy_type_4": 1,
    "not_specified|Congenital_generalized_lipodystrophy_type_4|not_provided": 1,
    "CAVIN1-related_disorder|Monogenic_diabetes|not_specified|not_provided|Congenital_generalized_lipodystrophy_type_4": 1,
    "not_provided|CAVIN1-related_disorder": 1,
    "not_specified|Congenital_generalized_lipodystrophy_type_4": 1,
    "Congenital_generalized_lipodystrophy_type_4|not_specified|not_provided": 1,
    "CAVIN1-related_disorder": 4,
    "CAVIN1-related_disorder|not_provided": 2,
    "CAVIN1-related_disorder|Monogenic_diabetes|not_provided|See_cases": 1,
    "CAVIN1-related_disorder|not_provided|Congenital_generalized_lipodystrophy_type_4|not_specified": 1,
    "Monogenic_diabetes|Congenital_generalized_lipodystrophy_type_4|not_provided": 1,
    "CAVIN1-related_disorder|not_provided|Congenital_generalized_lipodystrophy_type_4": 2,
    "Congenital_generalized_lipodystrophy_type_4|CAVIN1-related_disorder": 1,
    "CAVIN1-related_disorder|not_provided|not_specified|Congenital_generalized_lipodystrophy_type_4|Monogenic_diabetes": 1,
    "Seizure|Global_developmental_delay|Developmental_and_epileptic_encephalopathy_104": 1,
    "Developmental_and_epileptic_encephalopathy_104": 15,
    "Neurodevelopmental_disorder_with_epilepsy_and_brain_atrophy": 8,
    "Developmental_and_epileptic_encephalopathy_104|Neurodevelopmental_disorder_with_epilepsy_and_brain_atrophy": 3,
    "Neurodevelopmental_disorder_with_epilepsy_and_brain_atrophy|Developmental_and_epileptic_encephalopathy_104|not_provided": 1,
    "ATP6V0A1-related_condition": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_104|Focal-onset_seizure|Intellectual_disability|Autism|Severe_global_developmental_delay|Cerebellar_ataxia|Lower_limb_spasticity|Microcephaly|Global_developmental_delay|Hypotonia|Large_for_gestational_age|Seizure|not_provided": 1,
    "Sanfilippo_syndrome|not_provided": 4,
    "Mucopolysaccharidosis|_MPS-III-B": 117,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_provided": 13,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 682,
    "NAGLU-related_disorder|not_specified|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 8,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 285,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 5,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_specified": 8,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Inborn_genetic_diseases|not_provided": 2,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_specified": 12,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 33,
    "Mucopolysaccharidosis|_MPS-III-B|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|Inborn_genetic_diseases": 4,
    "not_specified|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|NAGLU-related_disorder": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_provided": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 15,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Inborn_genetic_diseases": 7,
    "Mucopolysaccharidosis|_MPS-III-B|Mucopolysaccharidosistype_IIIB|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Intellectual_disability|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 6,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 9,
    "NAGLU-related_disorder": 3,
    "Hepatosplenomegaly|Mucopolysacchariduria|Intellectual_disability|_severe|Thick_eyebrow|Abnormality_of_metabolism/homeostasis|Coarse_facial_features|Abnormal_facial_shape|Hypertrichosis|not_provided|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Mucopolysaccharidosis|_MPS-III-B|not_provided": 2,
    "not_provided|not_specified|NAGLU-related_disorder|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Hypertrichosis|Intellectual_disability|_severe|Abnormal_facial_shape|Thick_eyebrow|Coarse_facial_features|Hepatosplenomegaly|Mucopolysacchariduria|Abnormality_of_metabolism/homeostasis|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-B|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-B|NAGLU-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2V": 4,
    "not_specified|not_provided|Mucopolysaccharidosis|_MPS-III-B": 1,
    "not_provided|NAGLU-related_disorder|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 2,
    "Mucopolysaccharidosis|_MPS-III-B|NAGLU-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "not_provided|Mucopolysaccharidosistype_IIIB|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Intellectual_disability": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|Mucopolysaccharidosis|not_provided": 2,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided|not_specified": 1,
    "Tip-toe_gait|not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|NAGLU-related_disorder": 2,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Tip-toe_gait|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Mucopolysaccharidosis|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Mucopolysaccharidosis|_MPS-III-B|not_provided|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_provided|See_cases": 1,
    "Mucopolysaccharidosis|_MPS-III-B|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2V": 3,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|NAGLU-related_disorder|not_provided": 1,
    "NAGLU-related_disorder|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 2,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosistype_IIIB": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2V": 4,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-B|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2V|NAGLU-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Mucopolysaccharidosis|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided|NAGLU-related_disorder": 1,
    "Inborn_genetic_diseases|Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-B|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_provided|NAGLU-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Sanfilippo_syndrome|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-B|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_specified|not_provided": 2,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_provided|Mucopolysaccharidosis": 1,
    "Intellectual_disability|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided": 1,
    "Mucopolysaccharidosis|not_provided|Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|NAGLU-related_disorder": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-B": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-B|Charcot-Marie-Tooth_disease_axonal_type_2V|not_provided|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_specified|NAGLU-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2V|Mucopolysaccharidosis|_MPS-III-B|not_specified|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_6": 168,
    "Neurodegeneration_with_brain_iron_accumulation_6|not_provided|COASY-related_disorder": 1,
    "Neurodegeneration_with_brain_iron_accumulation_6|not_specified|not_provided": 6,
    "Neurodegeneration_with_brain_iron_accumulation_6|not_specified": 16,
    "Neurodegeneration_with_brain_iron_accumulation_6|Pontocerebellar_hypoplasia|_type_12|not_specified": 2,
    "COASY-related_disorder|Neurodegeneration_with_brain_iron_accumulation_6|not_provided": 1,
    "not_specified|Neurodegeneration_with_brain_iron_accumulation_6": 14,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_6|Pontocerebellar_hypoplasia|_type_12|not_specified": 1,
    "Neurodegeneration_with_brain_iron_accumulation_6|COASY-related_disorder": 3,
    "not_provided|COASY-related_disorder|Neurodegeneration_with_brain_iron_accumulation_6": 3,
    "not_provided|Pontocerebellar_hypoplasia|_type_12|Neurodegeneration_with_brain_iron_accumulation_6|not_specified": 2,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_6|not_specified": 5,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_6": 9,
    "Neurodegeneration_with_brain_iron_accumulation_6|not_provided": 8,
    "not_provided|not_specified|Neurodegeneration_with_brain_iron_accumulation_6": 2,
    "not_specified|Neurodegeneration_with_brain_iron_accumulation_6|not_provided": 1,
    "Pontocerebellar_hypoplasia|_type_12": 2,
    "Neurodegeneration_with_brain_iron_accumulation_6|Neurodegeneration_with_brain_iron_accumulation": 1,
    "See_cases|Neurodegeneration_with_brain_iron_accumulation_6|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_6|COASY-related_disorder|not_provided": 1,
    "not_specified|not_provided|Neurodegeneration_with_brain_iron_accumulation_6": 3,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_6|Pontocerebellar_hypoplasia|_type_12": 1,
    "Lipid_storage_myopathy|COASY-Related_Disorders|Neurodegeneration_with_brain_iron_accumulation_6": 1,
    "not_provided|Pontocerebellar_hypoplasia|_type_12|Neurodegeneration_with_brain_iron_accumulation_6": 1,
    "COASY-related_disorder": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation|Pontocerebellar_hypoplasia|_type_12|Neurodegeneration_with_brain_iron_accumulation_6": 1,
    "Pontocerebellar_hypoplasia|_type_12|Neurodegeneration_with_brain_iron_accumulation_6": 2,
    "COASY-related_disorder|not_provided|Neurodegeneration_with_brain_iron_accumulation_6|Pontocerebellar_hypoplasia|_type_12": 1,
    "Neurodegeneration_with_brain_iron_accumulation_6|Pontocerebellar_hypoplasia|_type_12|not_provided|Neurodegeneration_with_brain_iron_accumulation|Congenital_cerebellar_hypoplasia|COASY-related_disorder|not_specified": 1,
    "COASY-related_disorder|Neurodegeneration_with_brain_iron_accumulation_6": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_6|COASY-related_disorder|not_specified": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_2B|Pontocerebellar_hypoplasia|_type_12": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Neurodegeneration_with_brain_iron_accumulation_6|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia|_type_12|Neurodegeneration_with_brain_iron_accumulation": 1,
    "COASY-Related_Disorders|Neurodegeneration_with_brain_iron_accumulation_6": 1,
    "PSMC3IP-related_disorder|not_provided": 1,
    "Ovarian_dysgenesis_3": 4,
    "PSMC3IP-related_disorder": 1,
    "not_provided|PSMC3IP-related_disorder": 2,
    "Ovarian_dysgenesis_3|not_provided": 3,
    "TUBG1-related_disorder": 6,
    "Complex_cortical_dysplasia_with_other_brain_malformations_4": 17,
    "TUBG1-related_disorder|not_provided": 1,
    "not_specified|TUBG1-related_disorder": 1,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_4": 3,
    "not_specified|Lissencephaly|not_provided": 1,
    "Complex_cortical_dysplasia_with_other_brain_malformations_4|not_provided": 2,
    "not_provided|Complex_cortical_dysplasia_with_other_brain_malformations_4|not_specified": 1,
    "not_provided|TUBG1-related_disorder": 1,
    "TUBG1-related_disorder|not_specified|not_provided": 1,
    "CNTNAP1-related_disorder": 12,
    "not_provided|Neuropathy|_congenital_hypomyelinating|_3|Lethal_congenital_contracture_syndrome_7": 2,
    "CNTNAP1-related_disorder|not_provided": 9,
    "Lethal_congenital_contracture_syndrome_7|Neuropathy|_congenital_hypomyelinating|_3|not_provided": 4,
    "Neuropathy|_congenital_hypomyelinating|_3": 11,
    "Lethal_congenital_contracture_syndrome_7|Neuropathy|_congenital_hypomyelinating|_3": 1,
    "Lethal_congenital_contracture_syndrome_7": 7,
    "Neuropathy|_congenital_hypomyelinating|_3|Lethal_congenital_contracture_syndrome_7|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4E|Inborn_genetic_diseases": 1,
    "Neuropathy|_congenital_hypomyelinating|_3|not_provided": 2,
    "not_provided|Lethal_congenital_contracture_syndrome_7": 3,
    "not_provided|CNTNAP1-related_disorder": 5,
    "Inborn_genetic_diseases|Lethal_congenital_contracture_syndrome_7|Neuropathy|_congenital_hypomyelinating|_3|not_provided": 1,
    "Inborn_genetic_diseases|Neuropathy|_congenital_hypomyelinating|_3|not_provided": 1,
    "Neuropathy|_congenital_hypomyelinating|_3|not_provided|Arthrogryposis|_distal|_type_1A": 1,
    "CNTNAP1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|CNTNAP1-related_disorder": 1,
    "not_provided|Neuropathy|_congenital_hypomyelinating|_3": 1,
    "Lethal_congenital_contracture_syndrome_7|not_provided": 1,
    "not_provided|Lethal_congenital_contracture_syndrome_7|Neuropathy|_congenital_hypomyelinating|_3": 1,
    "Neuropathy|_congenital_hypomyelinating|_3|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Neuropathy|_congenital_hypomyelinating|_3|Lethal_congenital_contracture_syndrome_7": 1,
    "Congenital_hypomyelination_neuropathy_with_or_without_arthrogryposis": 1,
    "not_provided|CNTNAP1-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_hypomyelination_neuropathy_with_or_without_arthrogryposis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Neuropathy|_congenital_hypomyelinating|_3|Inborn_genetic_diseases": 1,
    "Neuropathy|_congenital_hypomyelinating|_3|Lethal_congenital_contracture_syndrome_7": 1,
    "not_provided|EZH1-neurodevelopmental_syndrome": 2,
    "EZH1-neurodevelopmental_syndrome": 2,
    "EZH1-neurodevelopmental_syndrome|EZH1-related_disorder|not_provided": 1,
    "RAMP2-related_disorder": 1,
    "not_provided|VPS25-related_neurodevelopmental_delay": 1,
    "not_specified|VPS25-related_neurodevelopmental_delay": 1,
    "VPS25-related_neurodevelopmental_delay": 1,
    "Pseudohypoaldosteronism_type_2B": 161,
    "Inborn_genetic_diseases|not_provided|Pseudohypoaldosteronism_type_2B": 3,
    "Pseudohypoaldosteronism_type_2B|WNK4-related_disorder|not_provided": 4,
    "Pseudohypoaldosteronism_type_2B|Inborn_genetic_diseases": 21,
    "Pseudohypoaldosteronism_type_2B|not_provided": 34,
    "WNK4-related_disorder": 5,
    "not_provided|Pseudohypoaldosteronism_type_2B": 21,
    "WNK4-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Pseudohypoaldosteronism_type_2B": 1,
    "not_provided|Pseudohypoaldosteronism_type_2B|Inborn_genetic_diseases": 1,
    "Pseudohypoaldosteronism_type_2B|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2B": 3,
    "Pseudohypoaldosteronism_type_2B|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2B|not_provided": 3,
    "Pseudohypoaldosteronism_type_2A|not_provided|Pseudohypoaldosteronism_type_2B": 1,
    "WNK4-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2B": 8,
    "Pseudohypoaldosteronism_type_2B|not_provided|not_specified": 4,
    "not_provided|Pseudohypoaldosteronism_type_2B|not_specified": 2,
    "not_provided|not_specified|Pseudohypoaldosteronism_type_2B": 2,
    "WNK4-related_disorder|not_provided|Pseudohypoaldosteronism_type_2B": 1,
    "not_specified|not_provided|Pseudohypoaldosteronism_type_2B": 1,
    "not_specified|Pseudohypoaldosteronism_type_2B": 1,
    "WNK4-related_disorder|Pseudohypoaldosteronism_type_2B|not_provided": 1,
    "Pseudohypoaldosteronism_type_2B|Inborn_genetic_diseases|Pseudohypoaldosteronism_type_2A": 1,
    "not_provided|WNK4-related_disorder": 2,
    "Pseudohypoaldosteronism_type_2B|WNK4-related_disorder|not_specified|not_provided": 1,
    "Pseudohypoaldosteronism_type_2B|WNK4-related_disorder": 1,
    "COA3-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_14": 1,
    "COA3-related_disorder|not_provided": 1,
    "not_provided|not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_14": 1,
    "not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|G6PC1-related_disorder": 1,
    "G6PC1-related_disorder|not_specified|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 1,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 449,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided": 10,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_specified": 18,
    "G6PC1-related_disorder|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided|Glycogen_storage_disease|_type_I": 1,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided|not_specified": 2,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_specified|not_provided": 1,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|G6PC1-related_disorder|not_specified": 1,
    "not_specified|not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 4,
    "not_specified|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 19,
    "not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 20,
    "Glycogen_storage_disease|_type_I|not_specified|not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|Glycogen_storage_disease|Hypoglycemia|Short_stature": 1,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|Inborn_genetic_diseases": 2,
    "G6PC1-related_disorder": 1,
    "G6PC1-related_disorder|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|Glycogen_storage_disease|_type_I|not_specified|not_provided": 1,
    "not_provided|not_specified|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 3,
    "Glycogen_storage_disease|_type_I|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided": 1,
    "G6PC1-related_disorder|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 2,
    "Glycogen_storage_disease|_type_I|not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 1,
    "G6PC1-related_disorder|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided|not_specified": 1,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|G6PC1-related_disorder": 1,
    "not_specified|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided": 2,
    "Increased_hepatic_glycogen_content": 1,
    "Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_specified|not_provided|G6PC1-related_disorder": 1,
    "not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_specified": 1,
    "Glycogen_storage_disease|_type_I|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA": 1,
    "G6PC1-related_disorder|not_specified|not_provided|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|Glycogen_storage_disease": 1,
    "Diamond-Blackfan_anemia_16": 2,
    "RPL27-related_disorder": 3,
    "not_provided|RPL27-related_disorder": 2,
    "not_provided|Diamond-Blackfan_anemia_16": 1,
    "not_specified|Diamond-Blackfan_anemia_16|not_provided": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided": 3,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 9,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 209,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 33,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 179,
    "BRCA1-related_disorder": 16,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "not_specified|BRCA1-related_disorder": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 4,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 81,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 2,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 10,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 28,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 14,
    "not_provided|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "not_provided|BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 18,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 57,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 123,
    "NICE_approved_PARP_inhibitor_treatment|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Fanconi_anemia|_complementation_group_S": 23,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 34,
    "not_provided|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 12,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 281,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 19,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 340,
    "not_specified|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 113,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 10,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 35,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 30,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Uterine_corpus_cancer": 1,
    "BRCA1-related_cancer_predisposition|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 11,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 14,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Gastric_cancer|Lung_cancer|Ovarian_neoplasm|Breast_neoplasm|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 18,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|See_cases": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 13,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 19,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 11,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 7,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 50,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Colorectal_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 6,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_neoplasm|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 25,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_urinary_bladder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 15,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 16,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Ovarian_cancer": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 14,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 5,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 7,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 31,
    "not_specified|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Lynch_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|BRCA1-related_cancer_predisposition": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 9,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast": 8,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 6,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 9,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Triple-negative_breast_cancer": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 16,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "not_specified|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition": 19,
    "BRCA1-related_disorder|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition": 7,
    "not_specified|not_provided|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "not_provided|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_disorder": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Carcinoma_of_colon": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Punctate_palmoplantar_keratoderma_type_2|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Pancreatic_cancer|_susceptibility_to|Endometrial_carcinoma|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 13,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 5,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 8,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 15,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 12,
    "Hereditary_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 10,
    "Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|not_provided|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|not_specified": 1,
    "BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Breast_and/or_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 4,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 3,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_provided|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 3,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 7,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 14,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 13,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|Lynch_syndrome_1|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and_colorectal_cancer|Ovarian_cancer|Endometrial_carcinoma|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast|Fanconi_anemia|_complementation_group_S|not_provided|Fanconi_anemia_complementation_group_A": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "BRCA1-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 5,
    "not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|BRCA1-related_cancer_predisposition": 2,
    "not_provided|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 9,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 13,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 21,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Gastric_cancer|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition": 6,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Breast_and/or_ovarian_cancer|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 6,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Malignant_tumor_of_breast|Inherited_ovarian_cancer_(without_breast_cancer)|BRCA1-related_cancer_predisposition|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 17,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 5,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 4,
    "not_specified|not_provided|Malignant_tumor_of_breast|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_neoplasm|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified": 2,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 7,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 7,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "not_specified|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_specified|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided|Malignant_tumor_of_breast|BRCA1-related_cancer_predisposition|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 5,
    "Hereditary_cancer-predisposing_syndrome|Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 9,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 6,
    "not_provided|Breast_and/or_ovarian_cancer|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ovarian_carcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 3,
    "Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4": 3,
    "Malignant_tumor_of_pancreas|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 2,
    "not_provided|Familial_cancer_of_breast|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA1-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 5,
    "BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Carcinoma_of_head_of_pancreas": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Familial_prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Inherited_breast_cancer_and_ovarian_cancer|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 10,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 3,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "BRCA1-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Breast_and/or_ovarian_cancer|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition": 1,
    "BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 1,
    "BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ovarian_cancer|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Triple-negative_breast_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 2,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition": 5,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Inherited_breast_cancer_and_ovarian_cancer|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 3,
    "Breast_and/or_ovarian_cancer|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Breast_and/or_ovarian_cancer|not_provided|BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Inherited_breast_cancer_and_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 8,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma": 2,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "BRCA1-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA1-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_specified": 1,
    "Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|Carcinoma_of_pancreas|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 8,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_pancreatic_carcinoma|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Familial_cancer_of_breast|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 2,
    "not_provided|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 3,
    "Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Abnormality_of_the_ovary|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Familial_cancer_of_breast|Ovarian_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "BRCA1-related_disorder|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Peritoneum_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided": 1,
    "BRCA1-related_disorder|Breast_neoplasm|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_provided|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 4,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "not_provided|Breast_and/or_ovarian_cancer|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Gastric_cancer|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_serous_surface_papillary_adenocarcinoma|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Inherited_ovarian_cancer_(without_breast_cancer)|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Malignant_tumor_of_urinary_bladder|Familial_cancer_of_breast|Ovarian_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|not_provided|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_disorder|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Infiltrating_duct_carcinoma_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Ovarian_cancer|not_specified|Familial_cancer_of_breast|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|BRCA1-related_cancer_predisposition|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_pancreatic_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "BRCA1-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Breast_cancer|_susceptibility_to|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Malignant_tumor_of_pancreas|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "BRCA1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_carcinoma": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 5,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition": 1,
    "BRCA1-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Burkitt_lymphoma": 1,
    "BRCA1-related_disorder|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Gastric_cancer": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 2,
    "Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_urinary_bladder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Ovarian_carcinoma": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_breast_and_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ovarian_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_disorder": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm": 1,
    "Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Endometrial_carcinoma|Familial_cancer_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 2,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_disorder|BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|NICE_approved_PARP_inhibitor_treatment|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|not_specified": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ovarian_carcinoma": 2,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA1-related_cancer_predisposition": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Infiltrating_duct_carcinoma_of_breast|Fanconi_anemia|_complementation_group_S|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_pancreas|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "BRCA1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Endometrial_carcinoma|Breast_carcinoma": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_specified|not_provided": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_cancer_predisposition|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Dysgerminoma|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast|bilateral_breast_cancer": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|BRCA1-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Ovarian_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast_ductal_adenocarcinoma|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BRCA1-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Rhabdomyosarcoma|not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Fanconi_anemia|_complementation_group_S|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_pancreatic_carcinoma|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_neoplasm|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "Ovarian_cancer|Malignant_tumor_of_pancreas|Hereditary_cancer-predisposing_syndrome|not_specified|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Periventricular_nodular_heterotopia|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Inherited_breast_cancer_and_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_carcinoma|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia|_complementation_group_S|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|Fanconi_anemia_complementation_group_A|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Gastric_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ovarian_carcinoma": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|Inherited_ovarian_cancer_(without_breast_cancer)|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and/or_ovarian_cancer": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|BRCA1-related_cancer_predisposition|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Gastric_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Endometrial_carcinoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Inherited_ovarian_cancer_(without_breast_cancer)|Breast_and/or_ovarian_cancer|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast_cancer|_susceptibility_to": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and/or_ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Inherited_breast_cancer_and_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S": 1,
    "BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|BRCA1-related_cancer_predisposition|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_disorder": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia|_complementation_group_S|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Pancreatic_cancer|_susceptibility_to|_4|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_urinary_bladder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|BRCA1-related_cancer_predisposition|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|not_provided": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast|Familial_cancer_of_breast": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|BRCA1-related_cancer_predisposition|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Invasive_medullary_breast_carcinoma|BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Fanconi_anemia|_complementation_group_S|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Endometrial_carcinoma|Familial_cancer_of_breast|Malignant_tumor_of_breast|Triple-negative_breast_cancer": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Familial_cancer_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Infant-type_hemispheric_glioma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Ovarian_neoplasm|BRCA1-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S|Pancreatic_cancer|_susceptibility_to|_4|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRCA1-related_cancer_predisposition|BRCA1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|BRCA1-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "BRCA1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia|_complementation_group_S|Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia|_complementation_group_S": 1,
    "BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_specified|Familial_cancer_of_breast|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Malignant_tumor_of_breast": 1,
    "BRCA1-related_disorder|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Pancreatic_cancer|_susceptibility_to|_4|Fanconi_anemia|_complementation_group_S|Hereditary_cancer-predisposing_syndrome": 1,
    "BRCA1-related_disorder|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and/or_ovarian_cancer|not_specified|Malignant_tumor_of_breast|not_provided": 1,
    "ETV4-related_disorder": 3,
    "MEOX1-related_disorder|not_provided": 3,
    "not_provided|MEOX1-related_disorder": 1,
    "Klippel-Feil_syndrome_2|_autosomal_recessive": 5,
    "MEOX1-related_disorder": 2,
    "Sclerosteosis_1": 37,
    "Primary_bone_dysplasia_with_increased_bone_density": 4,
    "not_provided|Sclerosteosis_1": 4,
    "Sclerosteosis_1|not_provided": 7,
    "SOST-related_disorder": 2,
    "Inborn_genetic_diseases|SOST-related_disorder": 1,
    "Sclerosteosis_1|Craniodiaphyseal_dysplasia|_autosomal_dominant": 1,
    "SOST-related_disorder|not_provided": 1,
    "Primary_bone_dysplasia_with_increased_bone_density|not_provided": 1,
    "Craniodiaphyseal_dysplasia|_autosomal_dominant": 1,
    "Craniodiaphyseal_dysplasia|_autosomal_dominant|SOST-related_disorder": 1,
    "not_provided|SOST-related_disorder|Sclerosteosis_1": 1,
    "not_provided|Sclerosteosis_1|not_specified|SOST-related_disorder": 1,
    "Hyperammonemia|_type_III|not_specified": 11,
    "Hyperammonemia|_type_III": 552,
    "Hyperammonemia|_type_III|not_provided": 7,
    "Hyperammonemia|_type_III|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|not_provided|Hyperammonemia|_type_III": 1,
    "Inborn_genetic_diseases|Hyperammonemia|_type_III": 14,
    "not_provided|Hyperammonemia|_type_III": 8,
    "not_specified|Hyperammonemia|_type_III|NAGS-related_disorder|not_provided": 1,
    "not_specified|Hyperammonemia|_type_III": 3,
    "NAGS-related_disorder": 3,
    "not_provided|Hyperammonemia|_type_III|NAGS-related_disorder": 1,
    "not_specified|Hyperammonemia|_type_III|NAGS-related_disorder": 1,
    "not_provided|not_specified|Hyperammonemia|_type_III": 1,
    "not_specified|not_provided|Hyperammonemia|_type_III": 3,
    "not_provided|Inborn_genetic_diseases|Hyperammonemia|_type_III": 2,
    "not_provided|Hyperammonemia|_type_III|NAGS-related_disorder|Inborn_genetic_diseases": 1,
    "Hyperammonemia|_type_III|NAGS-related_disorder|not_provided": 1,
    "Hyperammonemia|_type_III|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|NAGS-related_disorder": 1,
    "NAGS-related_disorder|not_provided|Hyperammonemia|_type_III": 1,
    "Hyperammonemia|_type_III|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 231,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 12,
    "G6PC3-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 2,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 60,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases": 67,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|G6PC3-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|not_provided": 9,
    "not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 2,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|not_specified": 1,
    "not_specified|G6PC3-related_disorder|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases": 1,
    "G6PC3-related_disorder|Inborn_genetic_diseases|not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|not_provided": 1,
    "not_specified|not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 1,
    "not_provided|not_specified|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 2,
    "G6PC3-related_disorder|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 1,
    "not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 2,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases|not_specified|G6PC3-related_disorder": 1,
    "G6PC3-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "G6PC3-related_disorder|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inherited_Immunodeficiency_Diseases": 1,
    "Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "G6PC3-related_disorder|not_specified|not_provided|Autosomal_recessive_severe_congenital_neutropenia_due_to_G6PC3_deficiency": 1,
    "Ovarian_dysgenesis_11|Premature_ovarian_insufficiency": 1,
    "Ovarian_dysgenesis_11": 2,
    "HAREL-TORA_NEURODEVELOPMENTAL_SYNDROME|See_cases": 1,
    "Childhood-onset_motor_and_cognitive_regression_syndrome_with_extrapyramidal_movement_disorder": 16,
    "UBTF-related_disorder|not_specified": 1,
    "UBTF-related_disorder": 9,
    "Inborn_genetic_diseases|UBTF-related_disorder": 1,
    "Inborn_genetic_diseases|Childhood-onset_motor_and_cognitive_regression_syndrome_with_extrapyramidal_movement_disorder": 1,
    "UBTF-related_disorder|not_provided": 2,
    "Infantile_or_childhood_onset_neurodegenerative_disease|_global_developmental_delay|_and_intellectual_disability|Childhood-onset_motor_and_cognitive_regression_syndrome_with_extrapyramidal_movement_disorder|UBTF_E210K_Neuroregression_Syndrome|Inborn_genetic_diseases|UBTF-related_disorder|Rare_syndromic_intellectual_disability|not_provided|See_cases": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia|Hereditary_spherocytosis_type_4": 7,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis": 12,
    "Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4": 2,
    "Autosomal_dominant_distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|Hemolytic_anemia": 11,
    "Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia|not_provided": 6,
    "Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia": 18,
    "Hemolytic_anemia|Distal_Renal_Tubular_Acidosis|_Dominant|Spherocytosis|_Dominant": 4,
    "Distal_Renal_Tubular_Acidosis|_Dominant|Hemolytic_anemia|Spherocytosis|_Dominant|not_provided": 1,
    "Hemolytic_anemia|Distal_Renal_Tubular_Acidosis|_Dominant|Spherocytosis|_Dominant|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|not_provided|Autosomal_dominant_distal_renal_tubular_acidosis": 3,
    "Hemolytic_anemia|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis": 3,
    "Distal_Renal_Tubular_Acidosis|_Dominant|Hemolytic_anemia|Spherocytosis|_Dominant": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 10,
    "Hereditary_spherocytosis_type_4|BLOOD_GROUP--DIEGO_SYSTEM|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--FROESE|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WRIGHT_ANTIGEN|Hemolytic_anemia": 2,
    "not_provided|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "not_provided|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|BLOOD_GROUP--FROESE|Autosomal_dominant_distal_renal_tubular_acidosis|Southeast_Asian_ovalocytosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN": 1,
    "not_specified|Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hemolytic_anemia|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_distal_renal_tubular_acidosis": 2,
    "not_provided|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Malaria|_susceptibility_to": 1,
    "Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia": 3,
    "Autosomal_dominant_distal_renal_tubular_acidosis": 7,
    "not_provided|not_specified|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia": 3,
    "Inborn_genetic_diseases|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "Hereditary_spherocytosis_type_4|not_provided": 2,
    "Hereditary_spherocytosis_type_4|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--FROESE|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 2,
    "Hereditary_spherocytosis_type_4|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--FROESE|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 39,
    "Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Renal_tubular_acidosis": 1,
    "Southeast_Asian_ovalocytosis|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|Hereditary_spherocytosis_type_4|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_4": 8,
    "Hereditary_spherocytosis_type_4|not_provided|not_specified|SLC4A1-related_disorder|Hemolytic_anemia|Acanthocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Acanthocytosis_due_to_band_3_HT": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia|not_specified": 2,
    "Distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|not_specified|Hereditary_spherocytosis_type_4|not_provided|Hemolytic_anemia|DIEGO_BLOOD_GROUP_ANTIGEN": 1,
    "not_provided|Hemolytic_anemia|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "Hereditary_spherocytosis_type_4": 17,
    "Cryohydrocytosis": 4,
    "not_provided|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|Hereditary_spherocytosis_type_4|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|SLC4A1-related_disorder": 1,
    "not_provided|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 1,
    "SLC4A1-related_disorder": 14,
    "Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "Hemolytic_anemia|Inborn_genetic_diseases|not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|not_provided": 1,
    "Renal_tubular_acidosis": 1,
    "BLOOD_GROUP--WRIGHT_ANTIGEN|Cryohydrocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|BLOOD_GROUP--DIEGO_SYSTEM|Inborn_genetic_diseases": 3,
    "not_provided|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to": 1,
    "not_specified|not_provided|SLC4A1-related_disorder|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|Cryohydrocytosis": 1,
    "Southeast_Asian_ovalocytosis|Cryohydrocytosis|Malaria|_susceptibility_to|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|not_provided|Inborn_genetic_diseases": 1,
    "Renal_tubular_acidosis|_distal|_with_normal_red_cell_morphology": 1,
    "Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--SWANN_SYSTEM|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 3,
    "SLC4A1-related_disorder|not_provided|Hereditary_spherocytosis_type_4": 1,
    "SLC4A1-related_disorder|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|not_provided": 1,
    "BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Inborn_genetic_diseases": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--FROESE|Autosomal_dominant_distal_renal_tubular_acidosis|Southeast_Asian_ovalocytosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|Distal_Renal_Tubular_Acidosis|_Dominant|Spherocytosis|_Dominant": 1,
    "Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|not_provided": 1,
    "Cryohydrocytosis|not_provided": 3,
    "Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|not_provided|SLC4A1-related_disorder|Hemolytic_anemia": 1,
    "not_provided|Inborn_genetic_diseases|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Cryohydrocytosis|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Inborn_genetic_diseases": 1,
    "Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Inborn_genetic_diseases": 1,
    "Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 1,
    "Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|SLC4A1-related_disorder|not_provided": 1,
    "Hemolytic_anemia|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|not_provided": 2,
    "Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Southeast_Asian_ovalocytosis|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to|Inborn_genetic_diseases": 1,
    "Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to": 1,
    "Malaria|_susceptibility_to|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 3,
    "Inborn_genetic_diseases|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|not_specified|not_provided|Hemolytic_anemia": 1,
    "not_specified|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia|not_provided": 2,
    "not_specified|not_provided|Hereditary_spherocytosis_type_4|SWANN_BLOOD_GROUP_ANTIGEN|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia": 1,
    "not_provided|SWANN_BLOOD_GROUP_ANTIGEN": 1,
    "Renal_tubular_acidosis|not_provided|Southeast_Asian_ovalocytosis|Cryohydrocytosis|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to": 1,
    "Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "SLC4A1-related_disorder|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "not_provided|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4": 1,
    "Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_specified|not_provided": 1,
    "not_provided|Spherocytosis|Inborn_genetic_diseases|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Malaria|_susceptibility_to|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--FROESE|Southeast_Asian_ovalocytosis": 1,
    "SLC4A1-related_disorder|Distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Inborn_genetic_diseases|not_provided": 1,
    "Renal_tubular_acidosis|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--DIEGO_SYSTEM|Cryohydrocytosis|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|not_provided": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "not_provided|SLC4A1-related_disorder": 4,
    "SLC4A1-related_disorder|not_provided": 3,
    "not_provided|SLC4A1-related_disorder|Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|not_provided|Bronchiectasis_with_or_without_elevated_sweat_chloride_3": 1,
    "Cryohydrocytosis|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 2,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Malaria|_susceptibility_to|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--FROESE": 2,
    "Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubulopathies": 1,
    "Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Inborn_genetic_diseases|not_provided": 1,
    "Southeast_Asian_ovalocytosis|Cryohydrocytosis|Malaria|_susceptibility_to|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|not_provided": 1,
    "not_provided|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 1,
    "Inborn_genetic_diseases|not_provided|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Cryohydrocytosis|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to": 1,
    "Hereditary_spherocytosis_type_4|not_provided|SLC4A1-related_disorder": 1,
    "BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "BLOOD_GROUP--FROESE": 1,
    "Distal_Renal_Tubular_Acidosis|_Dominant|Spherocytosis|_Dominant|Hemolytic_anemia": 1,
    "Inborn_genetic_diseases|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--FROESE|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|not_provided": 1,
    "not_provided|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Cryohydrocytosis|Hereditary_spherocytosis_type_4": 1,
    "Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided|Hereditary_spherocytosis_type_4": 1,
    "Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia|not_specified|not_provided": 1,
    "Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to|not_provided": 1,
    "Inborn_genetic_diseases|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "not_provided|Southeast_Asian_ovalocytosis|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to": 1,
    "SLC4A1-related_disorder|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Hemolytic_anemia|not_provided": 1,
    "not_provided|Autosomal_dominant_distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|Hemolytic_anemia": 2,
    "Distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided|Malaria|_cerebral|_resistance_to": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis|Inborn_genetic_diseases": 1,
    "not_provided|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Inborn_genetic_diseases": 1,
    "not_provided|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Malaria|_susceptibility_to|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spherocytosis_type_4|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Cryohydrocytosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to": 1,
    "Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|not_provided": 1,
    "not_provided|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Cryohydrocytosis|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|SLC4A1-related_disorder": 1,
    "not_provided|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4": 1,
    "BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Cryohydrocytosis": 1,
    "not_provided|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hemolytic_anemia": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|not_provided|Hereditary_spherocytosis_type_4|Hemolytic_anemia|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to": 1,
    "not_provided|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "Cryohydrocytosis|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Southeast_Asian_ovalocytosis|Hemolytic_anemia": 1,
    "not_specified|Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "not_provided|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Autosomal_recessive_distal_renal_tubular_acidosis": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--FROESE|Cryohydrocytosis|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_spherocytosis_type_4|BLOOD_GROUP--DIEGO_SYSTEM|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--FROESE|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WRIGHT_ANTIGEN|not_provided|Hemolytic_anemia": 1,
    "Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Cryohydrocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "not_provided|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|not_provided|Hereditary_spherocytosis_type_4|Hemolytic_anemia": 1,
    "not_provided|Hereditary_spherocytosis_type_4|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to": 1,
    "Hemolytic_anemia|not_provided|SLC4A1-related_disorder|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "not_specified|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|not_provided|Hemolytic_anemia": 1,
    "not_provided|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "not_provided|Inborn_genetic_diseases|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Cryohydrocytosis|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "not_provided|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Hereditary_spherocytosis_type_4|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Cryohydrocytosis|Malaria|_susceptibility_to": 1,
    "not_provided|Malaria|_susceptibility_to|Cryohydrocytosis|Southeast_Asian_ovalocytosis|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 1,
    "BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|not_provided|Inborn_genetic_diseases": 1,
    "Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spherocytosis_type_4|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--FROESE|Cryohydrocytosis": 1,
    "Hereditary_spherocytosis_type_4|BLOOD_GROUP--FROESE|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Southeast_Asian_ovalocytosis|Inborn_genetic_diseases": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--SWANN_SYSTEM|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|Hereditary_spherocytosis_type_4|not_provided": 1,
    "Hemolytic_anemia|Hereditary_spherocytosis_type_4|not_provided|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Southeast_Asian_ovalocytosis|Malaria|_susceptibility_to|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "not_provided|SLC4A1-related_disorder|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|Hereditary_spherocytosis_type_4|BLOOD_GROUP--DIEGO_SYSTEM": 1,
    "Autosomal_dominant_distal_renal_tubular_acidosis|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Cryohydrocytosis|Inborn_genetic_diseases|not_provided": 1,
    "Hemolytic_anemia|not_provided|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|BLOOD_GROUP--WALDNER_TYPE|Autosomal_dominant_distal_renal_tubular_acidosis|Cryohydrocytosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--SWANN_SYSTEM|Malaria|_susceptibility_to|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|SLC4A1-related_disorder|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 1,
    "not_provided|.|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia|not_specified": 1,
    "Distal_renal_tubular_acidosis|SLC4A1-related_disorder|Cryohydrocytosis|not_provided|Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|Hemolytic_anemia": 1,
    "BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|Hereditary_spherocytosis_type_4|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Malaria|_susceptibility_to|not_provided": 1,
    "not_provided|Hereditary_spherocytosis_type_4|Hemolytic_anemia|Autosomal_dominant_distal_renal_tubular_acidosis": 1,
    "not_provided|Malaria|_susceptibility_to|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|Southeast_Asian_ovalocytosis|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 1,
    "Hereditary_spherocytosis_type_4|Hemolytic_anemia|not_specified|Autosomal_dominant_distal_renal_tubular_acidosis|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Malaria|_susceptibility_to|BLOOD_GROUP--SWANN_SYSTEM|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|Southeast_Asian_ovalocytosis|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|SLC4A1-related_disorder|not_provided": 1,
    "Hereditary_spherocytosis_type_4|Autosomal_dominant_distal_renal_tubular_acidosis|SLC4A1-related_disorder|Hemolytic_anemia": 1,
    "Malaria|_susceptibility_to|Southeast_Asian_ovalocytosis|BLOOD_GROUP--WALDNER_TYPE|BLOOD_GROUP--FROESE|BLOOD_GROUP--WRIGHT_ANTIGEN|BLOOD_GROUP--DIEGO_SYSTEM|BLOOD_GROUP--SWANN_SYSTEM|Hereditary_spherocytosis_type_4|Cryohydrocytosis|Autosomal_dominant_distal_renal_tubular_acidosis|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia|not_provided|Hemolytic_anemia": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 25,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided": 4,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_specified|not_provided": 1,
    "not_specified|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_specified": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 309,
    "not_provided|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 9,
    "GRN-related_disorder": 8,
    "Neuronal_ceroid_lipofuscinosis_11": 1,
    "not_provided|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 19,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 60,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 23,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided": 13,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Inborn_genetic_diseases": 10,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Parkinsonian_disorder": 2,
    "not_provided|Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 4,
    "not_provided|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 5,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Frontotemporal_dementia": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided": 26,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided|GRN-related_disorder": 2,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|GRN-related_disorder|not_specified|Neuronal_ceroid_lipofuscinosis_11": 1,
    "not_specified|not_provided|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Frontotemporal_dementia|GRN-related_disorder": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Inborn_genetic_diseases|not_provided|GRN-related_disorder": 2,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Alzheimer_disease": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|GRN-related_disorder": 7,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|GRN-related_disorder": 2,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_specified": 2,
    "Inborn_genetic_diseases|GRN-related_disorder|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_3|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|GRN-related_disorder": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_specified|Neuronal_ceroid_lipofuscinosis_11|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|GRN-related_disorder|Frontotemporal_dementia|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided|not_specified": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Frontotemporal_dementia": 1,
    "GRN-related_disorder|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Inborn_genetic_diseases|not_provided": 1,
    "GRN-related_disorder|Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|GRN-related_disorder": 1,
    "not_provided|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Inborn_genetic_diseases": 2,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|GRN-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 4,
    "Inborn_genetic_diseases|GRN-related_disorder|not_provided|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Inborn_genetic_diseases": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "GRN-related_disorder|Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_specified": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided": 3,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided|Frontotemporal_dementia": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|GRN-related_disorder": 2,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|Primary_progressive_aphasia": 1,
    "GRN-related_disorder|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 2,
    "not_provided|Frontotemporal_dementia|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 2,
    "not_specified|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Frontotemporal_dementia": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|GRN-related_disorder|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|not_specified": 1,
    "GRN-related_disorder|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Frontotemporal_dementia": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Inborn_genetic_diseases|not_specified|not_provided|GRN-related_disorder": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided|Inborn_genetic_diseases": 2,
    "Cognitive_impairment|Frontotemporal_dementia": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided|Amyotrophic_lateral_sclerosis_type_10": 1,
    "GRN-related_disorder|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|GRN-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_provided": 2,
    "Inborn_genetic_diseases|GRN-related_disorder|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_specified|not_provided": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|GRN-related_disorder|Neuronal_ceroid_lipofuscinosis_11|not_provided|Inborn_genetic_diseases": 1,
    "Neuronal_ceroid_lipofuscinosis_11|not_provided": 1,
    "not_provided|GRN-related_disorder|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|Inborn_genetic_diseases": 3,
    "GRN-related_disorder|Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 1,
    "Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_specified": 2,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|not_specified|Inborn_genetic_diseases|GRN-related_disorder": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis|Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions": 1,
    "GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11|Primary_progressive_aphasia": 1,
    "GRN-related_disorder|not_specified|Inborn_genetic_diseases|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|Neuronal_ceroid_lipofuscinosis_11": 1,
    "Neuronal_ceroid_lipofuscinosis_11|GRN-related_frontotemporal_lobar_degeneration_with_Tdp43_inclusions|not_provided|FRONTOTEMPORAL_LOBAR_DEGENERATION_WITH_UBIQUITIN-POSITIVE_INCLUSIONS|_SUSCEPTIBILITY_TO|Ischemic_stroke": 1,
    "Glanzmann_thrombasthenia": 703,
    "Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia_1|ITGA2B-related_disorder|Glanzmann_thrombasthenia": 1,
    "Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia_1|Glanzmann_thrombasthenia": 3,
    "Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia": 2,
    "Inborn_genetic_diseases|Glanzmann_thrombasthenia": 8,
    "ITGA2B-related_disorder": 17,
    "not_specified|Glanzmann_thrombasthenia|Thrombocytopenia|Platelet-type_bleeding_disorder_16": 1,
    "ITGA2B-related_disorder|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia|Thrombocytopenia|not_provided": 1,
    "Platelet-type_bleeding_disorder_16": 10,
    "not_provided|Glanzmann_thrombasthenia|not_specified|Glanzmann_thrombasthenia_1": 1,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|not_provided|Abnormal_platelet_function": 1,
    "Glanzmann_thrombasthenia|not_provided": 21,
    "Inborn_genetic_diseases|Glanzmann_thrombasthenia|not_provided": 1,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1": 11,
    "ITGA2B-related_disorder|not_specified|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|not_provided": 1,
    "Inborn_genetic_diseases|Glanzmann_thrombasthenia|ITGA2B-related_disorder": 1,
    "Glanzmann_thrombasthenia_1|Glanzmann_thrombasthenia": 29,
    "not_provided|Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1": 2,
    "Glanzmann_thrombasthenia|not_specified": 16,
    "Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16": 5,
    "Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia": 3,
    "not_specified|Glanzmann_thrombasthenia|not_provided": 3,
    "Glanzmann_thrombasthenia_1": 19,
    "Glanzmann_thrombasthenia|Inborn_genetic_diseases": 22,
    "not_specified|Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1": 1,
    "ITGA2B-related_disorder|not_provided": 1,
    "not_provided|BAK_PLATELET-SPECIFIC_ANTIGEN|Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|not_specified": 1,
    "not_provided|ITGA2B-related_disorder|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16": 3,
    "not_specified|Glanzmann_thrombasthenia": 12,
    "Glanzmann_thrombasthenia|ITGA2B-related_disorder": 5,
    "Glanzmann_thrombasthenia|Platelet-type_bleeding_disorder_16": 3,
    "Glanzmann_thrombasthenia|Platelet-type_bleeding_disorder_16|ITGA2B-related_disorder|not_specified": 1,
    "ITGA2B-related_disorder|Glanzmann_thrombasthenia": 2,
    "ITGA2B-related_disorder|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia": 1,
    "not_specified|ITGA2B-related_disorder|Glanzmann_thrombasthenia|Inborn_genetic_diseases": 1,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|not_specified": 1,
    "Glanzmann_thrombasthenia|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Glanzmann_thrombasthenia|not_provided|Platelet-type_bleeding_disorder_16": 1,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|ITGA2B-related_disorder": 1,
    "Macrothrombocytopenia|Glanzmann_thrombasthenia": 2,
    "Glanzmann_thrombasthenia|not_specified|ITGA2B-related_disorder": 2,
    "Inborn_genetic_diseases|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia_1": 1,
    "Glanzmann_thrombasthenia|Abnormal_platelet_aggregation": 2,
    "Glanzmann_thrombasthenia|not_specified|not_provided": 4,
    "not_specified|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16": 1,
    "Glanzmann_thrombasthenia_1|not_provided|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia|ITGA2B-related_disorder|not_specified|not_provided": 1,
    "Glanzmann_thrombasthenia|not_provided|ITGA2B-related_disorder": 1,
    "ITGA2B-related_disorder|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia_1|Inborn_genetic_diseases": 1,
    "ITGA2B-related_disorder|Glanzmann_thrombasthenia_1|not_provided|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|not_provided": 1,
    "not_provided|Platelet-type_bleeding_disorder_16": 1,
    "not_provided|Glanzmann_thrombasthenia_1|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|not_provided|Glanzmann_thrombasthenia": 1,
    "not_provided|Glanzmann_thrombasthenia": 53,
    "Glanzmann_thrombasthenia|ITGA2B-related_disorder|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|not_specified": 1,
    "not_specified|not_provided|Glanzmann_thrombasthenia": 3,
    "Glanzmann_thrombasthenia|Inborn_genetic_diseases|not_specified": 1,
    "Glanzmann_thrombasthenia|ITGA2B-related_disorder|Glanzmann_thrombasthenia_1": 1,
    "not_specified|Glanzmann_thrombasthenia_1|Glanzmann_thrombasthenia|not_provided": 1,
    "not_provided|not_specified|Glanzmann_thrombasthenia": 3,
    "Glanzmann_thrombasthenia|ITGA2B-related_disorder|Glanzmann_thrombasthenia_1|not_provided": 1,
    "Glanzmann_thrombasthenia_1|Inborn_genetic_diseases": 2,
    "ITGA2B-related_disorder|not_specified|Glanzmann_thrombasthenia": 1,
    "Inborn_genetic_diseases|not_provided|Glanzmann_thrombasthenia": 2,
    "not_provided|Glanzmann_thrombasthenia_1|Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia": 1,
    "Inborn_genetic_diseases|Glanzmann_thrombasthenia|ITGA2B-related_disorder|not_specified|not_provided": 1,
    "Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia_1": 1,
    "not_provided|Inborn_genetic_diseases|Glanzmann_thrombasthenia": 1,
    "not_provided|FZD2-related_disorder": 4,
    "not_provided|not_specified|FZD2-related_disorder": 1,
    "Autosomal_dominant_omodysplasia": 6,
    "FZD2-related_disorder": 7,
    "FZD2-related_disorder|not_provided": 2,
    "not_provided|Autosomal_dominant_omodysplasia": 1,
    "Keratoconus|not_specified|not_provided": 1,
    "Autosomal_dominant_Robinow_syndrome_1|not_provided|Autosomal_dominant_Robinow_syndrome_2": 1,
    "Autosomal_dominant_Robinow_syndrome_3|Autosomal_dominant_omodysplasia": 1,
    "not_provided|Autosomal_dominant_Robinow_syndrome_1|Autosomal_dominant_omodysplasia|Autosomal_dominant_Robinow_syndrome_2": 1,
    "Mandibulofacial_dysostosis-microcephaly_syndrome": 94,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "EFTUD2-related_disorder": 8,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|not_provided": 7,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|not_provided|Hereditary_syndromic_Pierre_Robin_syndrome": 1,
    "not_provided|EFTUD2-related_disorder": 11,
    "not_provided|Mandibulofacial_dysostosis-microcephaly_syndrome": 7,
    "not_specified|not_provided|EFTUD2-related_disorder|Inborn_genetic_diseases": 1,
    "EFTUD2-related_disorder|not_provided": 8,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Mandibulofacial_dysostosis-microcephaly_syndrome": 2,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|not_provided|Mandibulofacial_dysostosis": 1,
    "Neurodevelopmental_disorder|Mandibulofacial_dysostosis-microcephaly_syndrome": 1,
    "not_specified|EFTUD2-related_disorder|not_provided": 1,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|Inborn_genetic_diseases|See_cases|not_provided": 1,
    "not_provided|not_specified|Mandibulofacial_dysostosis-microcephaly_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Mandibulofacial_dysostosis-microcephaly_syndrome": 1,
    "Mandibulofacial_dysostosis-microcephaly_syndrome|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Mandibulofacial_dysostosis-microcephaly_syndrome": 1,
    "not_specified|not_provided|Mandibulofacial_dysostosis-microcephaly_syndrome": 1,
    "Primary_ciliary_dyskinesia_17": 28,
    "not_provided|Primary_ciliary_dyskinesia_17": 3,
    "Primary_ciliary_dyskinesia_17|Primary_ciliary_dyskinesia": 7,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_17": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_17": 7,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_17": 2,
    "Primary_ciliary_dyskinesia|Diarrhea_12|_with_microvillus_atrophy": 1,
    "Infertility_disorder|Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia_17|Primary_ciliary_dyskinesia|CCDC103-related_disorder|not_provided": 1,
    "CCDC103-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Absent_inner_and_outer_dynein_arms|Situs_inversus|Primary_ciliary_dyskinesia_17": 1,
    "Primary_ciliary_dyskinesia_17|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_17": 1,
    "Alexander_disease|not_provided": 9,
    "not_provided|Alexander_disease": 83,
    "Alexander_disease": 59,
    "Inborn_genetic_diseases|not_provided|Alexander_disease": 2,
    "GFAP-related_disorder|not_provided": 6,
    "GFAP-related_disorder": 8,
    "not_provided|GFAP-related_disorder": 2,
    "Progressive_ventriculomegaly": 1,
    "not_specified|Alexander_disease|GFAP-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Alexander_disease": 1,
    "GFAP-related_disorder|not_specified|Inborn_genetic_diseases|Alexander_disease|not_provided": 1,
    "not_provided|not_specified|GFAP-related_disorder": 1,
    "not_provided|not_specified|GFAP-related_disorder|Alexander_disease": 1,
    "Spastic_paraplegia|_intellectual_disability|_nystagmus|_and_obesity|not_provided|Alexander_disease": 1,
    "GFAP-related_disorder|not_provided|Alexander_disease": 2,
    "not_specified|Alexander_disease": 2,
    "Alexander_disease|Inborn_genetic_diseases": 1,
    "GFAP-related_disorder|not_specified|not_provided": 1,
    "not_provided|Alexander_disease|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|GFAP-related_disorder": 1,
    "not_specified|Alexander_disease|not_provided": 1,
    "not_provided|Alexander_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Alexander_disease": 1,
    "NIK_deficiency": 419,
    "not_specified|not_provided|NIK_deficiency": 1,
    "NIK_deficiency|not_provided": 12,
    "not_provided|NIK_deficiency": 19,
    "MAP3K14-related_disorder": 5,
    "Immunodeficiency_112": 1,
    "NIK_deficiency|not_specified|not_provided": 2,
    "Immunodeficiency_112|NIK_deficiency": 1,
    "NIK_deficiency|MAP3K14-related_disorder": 1,
    "NIK_deficiency|not_provided|MAP3K14-related_disorder": 1,
    "not_specified|NIK_deficiency": 5,
    "not_provided|MAP3K14-related_disorder|NIK_deficiency": 1,
    "NIK_deficiency|not_specified": 2,
    "Osteopetrosis|_autosomal_dominant_3": 4,
    "Osteopetrosis|_autosomal_dominant_3|Autosomal_recessive_osteopetrosis_6|not_specified": 1,
    "Osteopetrosis|_autosomal_dominant_3|Autosomal_recessive_osteopetrosis_6|not_specified|not_provided": 1,
    "Autosomal_recessive_osteopetrosis_6": 1,
    "CRHR1-related_disorder": 2,
    "MAPT-Related_Spectrum_Disorders": 86,
    "MAPT-Related_Spectrum_Disorders|not_provided": 3,
    "not_provided|MAPT-Related_Spectrum_Disorders": 12,
    "not_specified|not_provided|MAPT-Related_Spectrum_Disorders": 1,
    "Frontotemporal_dementia|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|Supranuclear_palsy|_progressive|_1": 2,
    "MAPT-Related_Spectrum_Disorders|Frontotemporal_dementia": 6,
    "not_provided|Supranuclear_palsy|_progressive|_1": 3,
    "Pick_disease|Frontotemporal_dementia|Progressive_supranuclear_ophthalmoplegia|Parkinson_disease|_late-onset": 1,
    "not_specified|Frontotemporal_dementia|not_provided": 3,
    "MAPT-related_disorder|not_provided|Frontotemporal_dementia": 2,
    "Inborn_genetic_diseases|Frontotemporal_dementia": 1,
    "Frontotemporal_dementia|Inborn_genetic_diseases": 1,
    "Frontotemporal_dementia|Supranuclear_palsy|_progressive|_1|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease": 1,
    "Frontotemporal_dementia|not_specified": 1,
    "MAPT-related_disorder": 15,
    "Frontotemporal_dementia|not_provided|MAPT-related_disorder": 1,
    "Frontotemporal_dementia|MAPT-related_disorder|MAPT-Related_Spectrum_Disorders": 1,
    "not_specified|MAPT-Related_Spectrum_Disorders|Frontotemporal_dementia": 1,
    "MAPT-Related_Spectrum_Disorders|not_provided|Frontotemporal_dementia|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|Supranuclear_palsy|_progressive|_1|not_specified": 1,
    "MAPT-Related_Spectrum_Disorders|Frontotemporal_dementia|not_provided": 2,
    "MAPT-related_disorder|Frontotemporal_dementia": 2,
    "MAPT-related_disorder|not_provided": 3,
    "not_specified|not_provided|Frontotemporal_dementia": 6,
    "Frontotemporal_dementia|Pick_disease|Progressive_supranuclear_ophthalmoplegia": 1,
    "Pick_disease|Frontotemporal_dementia|Progressive_supranuclear_palsy-parkinsonism_syndrome|Supranuclear_palsy|_progressive|_1|Parkinson_disease|_late-onset": 1,
    "MAPT-related_disorder|not_provided|Frontotemporal_dementia|Progressive_supranuclear_ophthalmoplegia|Pick_disease|Multiple_system_atrophy": 1,
    "not_provided|MAPT-related_disorder|Frontotemporal_dementia": 2,
    "not_specified|not_provided|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|Supranuclear_palsy|_progressive|_1|Frontotemporal_dementia": 1,
    "MAPT-related_disorder|Frontotemporal_dementia|Supranuclear_palsy|_progressive|_1|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|not_provided": 1,
    "MAPT-related_disorder|not_specified|not_provided": 1,
    "Frontotemporal_dementia|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|Progressive_supranuclear_ophthalmoplegia|not_provided": 1,
    "Frontotemporal_dementia|not_specified|not_provided": 1,
    "not_provided|Frontotemporal_dementia|not_specified": 1,
    "Frontotemporal_dementia|Supranuclear_palsy|_progressive|_1": 1,
    "not_provided|not_specified|Frontotemporal_dementia": 2,
    "MAPT-related_disorder|Semantic_dementia": 1,
    "MAPT-related_disorder|not_provided|not_specified|Frontotemporal_dementia": 1,
    "not_provided|Frontotemporal_dementia|not_specified|MAPT-Related_Spectrum_Disorders": 1,
    "MAPT-Related_Spectrum_Disorders|not_provided|Frontotemporal_dementia": 3,
    "MAPT-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|MAPT-Related_Spectrum_Disorders": 1,
    "Frontotemporal_dementia|not_provided|MAPT-Related_Spectrum_Disorders|not_specified": 1,
    "Frontotemporal_dementia|MAPT-related_disorder": 5,
    "MAPT-Related_Spectrum_Disorders|Frontotemporal_dementia|not_specified|not_provided": 1,
    "Supranuclear_palsy|_progressive|_1|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|Frontotemporal_dementia": 1,
    "not_provided|Frontotemporal_dementia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|MAPT-Related_Spectrum_Disorders|Frontotemporal_dementia": 3,
    "MAPT-related_disorder|MAPT-Related_Spectrum_Disorders|not_provided|Frontotemporal_dementia|Progressive_supranuclear_palsy-parkinsonism_syndrome": 1,
    "not_provided|Frontotemporal_dementia|MAPT-Related_Spectrum_Disorders": 1,
    "Progressive_supranuclear_ophthalmoplegia|Frontotemporal_dementia|Pick_disease|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|not_provided": 1,
    "Supranuclear_palsy|_progressive|_1|Frontotemporal_dementia": 1,
    "Parkinson_disease|_late-onset|not_provided|Progressive_supranuclear_palsy-parkinsonism_syndrome": 1,
    "Frontotemporal_dementia|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Pick_disease|Supranuclear_palsy|_progressive|_1|not_provided": 1,
    "Supranuclear_palsy|_progressive|_1": 1,
    "MAPT-related_disorder|Supranuclear_palsy|_progressive|_1|Frontotemporal_dementia|Pick_disease|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|Progressive_supranuclear_ophthalmoplegia|not_provided": 1,
    "Frontotemporal_dementia|Mental_deterioration|Memory_impairment|not_provided|Progressive_supranuclear_palsy-parkinsonism_syndrome|Dementia|MAPT-related_disorder": 1,
    "Inborn_genetic_diseases|MAPT-related_disorder|not_specified|not_provided|Frontotemporal_dementia": 1,
    "not_provided|Frontotemporal_dementia|Pick_disease": 1,
    "MAPT-Related_Spectrum_Disorders|Frontotemporal_dementia|MAPT-related_disorder": 1,
    "Frontotemporal_dementia|MAPT-Related_Spectrum_Disorders": 1,
    "Pick_disease|Frontotemporal_dementia|not_provided": 1,
    "Early-onset_dementia_of_unclear_type|Frontotemporal_dementia": 1,
    "MAPT-related_disorder|Frontotemporal_dementia|Supranuclear_palsy|_progressive|_1|Pick_disease|Parkinson_disease|_late-onset|Progressive_supranuclear_palsy-parkinsonism_syndrome|not_provided": 1,
    "not_specified|Frontotemporal_dementia": 1,
    "MAPT-Related_Spectrum_Disorders|Syndromic_intellectual_disability": 27,
    "Syndromic_intellectual_disability|not_provided|MAPT-Related_Spectrum_Disorders": 2,
    "not_provided|Syndromic_intellectual_disability|MAPT-Related_Spectrum_Disorders": 10,
    "MAPT-Related_Spectrum_Disorders|Syndromic_intellectual_disability|not_provided": 1,
    "not_provided|Koolen-de_Vries_syndrome": 62,
    "Koolen-de_Vries_syndrome": 742,
    "Koolen-de_Vries_syndrome|Inborn_genetic_diseases": 27,
    "not_provided|Koolen-de_Vries_syndrome|not_specified": 2,
    "Koolen-de_Vries_syndrome|Inborn_genetic_diseases|not_specified": 2,
    "Koolen-de_Vries_syndrome|not_provided": 34,
    "not_provided|MAPT-Related_Spectrum_Disorders|Koolen-de_Vries_syndrome": 1,
    "Inborn_genetic_diseases|Koolen-de_Vries_syndrome": 25,
    "not_specified|Koolen-de_Vries_syndrome|Inborn_genetic_diseases": 3,
    "not_specified|Koolen-de_Vries_syndrome|not_provided": 2,
    "not_specified|Koolen-de_Vries_syndrome": 32,
    "Koolen-de_Vries_syndrome|not_specified": 51,
    "Inborn_genetic_diseases|not_provided|Koolen-de_Vries_syndrome": 7,
    "Inborn_genetic_diseases|not_specified|Koolen-de_Vries_syndrome": 3,
    "Inborn_genetic_diseases|Koolen-de_Vries_syndrome|not_specified": 4,
    "Koolen-de_Vries_syndrome|not_provided|Inborn_genetic_diseases": 8,
    "not_provided|Syndromic_intellectual_disability|MAPT-Related_Spectrum_Disorders|Koolen-de_Vries_syndrome": 3,
    "KANSL1-related_disorder": 12,
    "Dysplastic_corpus_callosum": 1,
    "KANSL1-related_disorder|Koolen-de_Vries_syndrome": 2,
    "KANSL1-related_disorder|Koolen-de_Vries_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Koolen-de_Vries_syndrome": 11,
    "not_provided|KANSL1-related_disorder|Koolen-de_Vries_syndrome": 1,
    "See_cases|Koolen-de_Vries_syndrome": 1,
    "not_specified|KANSL1-related_disorder|Koolen-de_Vries_syndrome": 1,
    "Koolen-de_Vries_syndrome|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Craniosynostosis_syndrome|not_provided|not_specified|Koolen-de_Vries_syndrome": 1,
    "Global_developmental_delay|Koolen-de_Vries_syndrome|not_provided": 1,
    "KANSL1-related_disorder|Koolen-de_Vries_syndrome|not_provided": 1,
    "not_provided|Koolen-de_Vries_syndrome|Inborn_genetic_diseases": 4,
    "not_provided|not_specified|Koolen-de_Vries_syndrome": 4,
    "KANSL1-related_disorder|Koolen-de_Vries_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Koolen-de_Vries_syndrome|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|Koolen-de_Vries_syndrome": 3,
    "not_provided|Inborn_genetic_diseases|Koolen-de_Vries_syndrome": 2,
    "not_provided|Congenital_myopathy|Inborn_genetic_diseases|not_specified|Koolen-de_Vries_syndrome": 1,
    "not_provided|Koolen-de_Vries_syndrome|Inborn_genetic_diseases|KANSL1-related_disorder|not_specified": 1,
    "Koolen-de_Vries_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Koolen-de_Vries_syndrome": 1,
    "Koolen-de_Vries_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|Inborn_genetic_diseases|not_specified|not_provided|Koolen-de_Vries_syndrome": 1,
    "Inborn_genetic_diseases|Koolen-de_Vries_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Koolen-de_Vries_syndrome|Intellectual_disability": 1,
    "Koolen-de_Vries_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_96": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy_96": 2,
    "WNT3-related_disorder|not_provided": 2,
    "not_provided|WNT3-related_disorder": 1,
    "Tetraamelia_syndrome_1": 1,
    "Renal_dysplasia|Chronic_kidney_disease|Renal_hypoplasia": 1,
    "WNT9B-related_disorder": 9,
    "not_provided|WNT9B-related_disorder": 2,
    "WNT9B-related_disorder|not_provided": 6,
    "Cystic_renal_dysplasia|Chronic_kidney_disease": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_6|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Progressive_myoclonic_epilepsy|not_provided|Progressive_myoclonic_epilepsy_type_6|not_specified": 1,
    "Muscular_dystrophy|_congenital|_with_or_without_seizures|not_provided": 1,
    "Muscular_dystrophy|_congenital|_with_or_without_seizures|Progressive_myoclonic_epilepsy_type_6": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy": 1,
    "not_provided|Progressive_myoclonic_epilepsy|GOSR2-related_disorder|Inborn_genetic_diseases|Muscular_dystrophy": 1,
    "Progressive_myoclonic_epilepsy|not_specified|not_provided|Progressive_myoclonic_epilepsy_type_6": 1,
    "Progressive_myoclonic_epilepsy|not_specified|Progressive_myoclonic_epilepsy_type_6": 1,
    "Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_specified": 2,
    "not_provided|Progressive_myoclonic_epilepsy|Muscular_dystrophy|_congenital|_with_or_without_seizures": 1,
    "developmental_delay_with_absent_seizures": 1,
    "Muscular_dystrophy|_congenital|_with_or_without_seizures|Progressive_myoclonic_epilepsy": 1,
    "Progressive_myoclonic_epilepsy|Progressive_myoclonic_epilepsy_type_6|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_specified|not_provided|Progressive_myoclonic_epilepsy_type_6": 1,
    "Progressive_myoclonic_epilepsy_type_6|not_specified|Myoclonic_epilepsy|_progressive|_X-linked|Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_provided": 1,
    "Progressive_myoclonic_epilepsy|not_specified|Inborn_genetic_diseases": 1,
    "Muscular_dystrophy|_congenital|_with_or_without_seizures|Progressive_myoclonic_epilepsy|not_provided|Progressive_myoclonic_epilepsy_type_6": 1,
    "Progressive_myoclonic_epilepsy_type_6|Muscular_dystrophy|_congenital|_with_or_without_seizures": 1,
    "Progressive_myoclonic_epilepsy|Progressive_myoclonic_epilepsy_type_6|Inborn_genetic_diseases": 1,
    "GOSR2-related_disorder|Muscular_dystrophy|_congenital|_with_or_without_seizures|Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|Progressive_myoclonic_epilepsy_type_6": 1,
    "Progressive_myoclonic_epilepsy_type_6|Progressive_myoclonic_epilepsy|not_specified|GOSR2-related_disorder": 1,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy": 1,
    "Progressive_myoclonic_epilepsy_type_6|Progressive_myoclonic_epilepsy|Muscular_dystrophy|_congenital|_with_or_without_seizures|Inborn_genetic_diseases|Muscular_dystrophy|not_provided": 1,
    "GOSR2-related_disorder": 2,
    "Progressive_myoclonic_epilepsy_type_6": 1,
    "Progressive_myoclonic_epilepsy|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy_type_6": 1,
    "not_provided|GOSR2-related_disorder|not_specified": 1,
    "not_specified|GOSR2-related_disorder": 1,
    "Atrial_fibrillation|_familial|_18": 198,
    "Atrial_fibrillation|_familial|_18|not_specified": 9,
    "Atrial_fibrillation|_familial|_18|Familial_atrial_fibrillation": 1,
    "not_specified|Atrial_fibrillation|_familial|_18": 7,
    "Atrial_fibrillation|_familial|_18|not_specified|not_provided": 2,
    "Atrial_fibrillation|_familial|_18|not_provided|MYL4-related_disorder": 2,
    "Atrial_fibrillation|_familial|_18|not_provided": 5,
    "not_provided|Atrial_fibrillation|_familial|_18|MYL4-related_disorder": 1,
    "MYL4-related_disorder": 1,
    "not_provided|Atrial_fibrillation|_familial|_18": 1,
    "Atrial_fibrillation|_familial|_18|MYL4-related_disorder": 2,
    "not_specified|Atrial_fibrillation|_familial|_18|not_provided": 1,
    "not_specified|MYL4-related_disorder|Atrial_fibrillation|_familial|_18": 1,
    "MYL4-related_disorder|Atrial_fibrillation|_familial|_18": 1,
    "not_provided|ITGB3-related_disorder": 6,
    "not_provided|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia": 5,
    "Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_2": 6,
    "not_provided|Inborn_genetic_diseases|ITGB3-related_disorder": 1,
    "Glanzmann_thrombasthenia_2|not_provided": 1,
    "Inborn_genetic_diseases|Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2": 1,
    "not_provided|Glanzmann_thrombasthenia_2": 3,
    "Glanzmann_thrombasthenia_2": 10,
    "Bleeding_disorder|_platelet-type|_24": 9,
    "not_specified|not_provided|PL(A1)/(A2)_ALLOANTIGEN_POLYMORPHISM|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia|not_specified|not_provided|Abnormal_bleeding|Thrombocytopenia|ITGB3-related_disorder": 1,
    "Glanzmann_thrombasthenia|not_specified|not_provided|ITGB3-related_disorder": 1,
    "ITGB3-related_disorder|not_provided": 3,
    "Bleeding_disorder|_platelet-type|_24|FETOMATERNAL_ALLOIMMUNE_THROMBOCYTOPENIA_1": 1,
    "not_provided|Glanzmann_thrombasthenia|not_specified": 4,
    "not_provided|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia": 1,
    "not_specified|not_provided|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|ITGB3-related_disorder|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_2|not_provided|Glanzmann_thrombasthenia": 6,
    "Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_1|not_provided|Glanzmann_thrombasthenia": 1,
    "Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_2|Glanzmann_thrombasthenia": 7,
    "Glanzmann_thrombasthenia_1|not_provided|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia_2|Glanzmann_thrombasthenia": 1,
    "not_specified|PEN(a)/PEN(b)_ALLOANTIGEN_POLYMORPHISM|not_provided|Glanzmann_thrombasthenia": 1,
    "Inborn_genetic_diseases|ITGB3-related_disorder": 1,
    "ITGB3-related_disorder|not_specified|Glanzmann_thrombasthenia|not_provided": 1,
    "ITGB3-related_disorder|Glanzmann_thrombasthenia|not_provided|not_specified": 1,
    "Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_2|not_provided|Glanzmann_thrombasthenia|Myocardial_infarction|_susceptibility_to|Bleeding_disorder|_platelet-type|_24": 1,
    "not_provided|Glanzmann_thrombasthenia|Glanzmann_thrombasthenia_1|Glanzmann_thrombasthenia_2": 1,
    "Glanzmann_thrombasthenia|not_provided|Inborn_genetic_diseases": 1,
    "Platelet-type_bleeding_disorder_16|not_provided|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_1|Glanzmann_thrombasthenia_2|not_provided|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|Platelet-type_bleeding_disorder_16|not_provided|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia_2|Glanzmann_thrombasthenia|not_provided|Myocardial_infarction|_susceptibility_to|Bleeding_disorder|_platelet-type|_24": 1,
    "Glanzmann_thrombasthenia|Abnormal_bleeding|Prolonged_bleeding_time|Platelet-type_bleeding_disorder_16": 1,
    "Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|not_provided|Glanzmann_thrombasthenia": 2,
    "Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|not_provided|Glanzmann_thrombasthenia": 2,
    "ITGB3-related_disorder": 4,
    "Glanzmann_thrombasthenia|Abnormal_bleeding": 1,
    "Glanzmann_thrombasthenia|ITGB3-related_disorder|not_specified|not_provided": 2,
    "not_provided|Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2": 1,
    "Glanzmann_thrombasthenia|not_provided|ITGB3-related_disorder": 4,
    "Platelet-type_bleeding_disorder_16|Glanzmann_thrombasthenia_2": 1,
    "not_provided|not_specified|Mo_ALLOANTIGEN_POLYMORPHISM": 1,
    "Fetal_and_neonatal_alloimmune_thrombocytopenia": 1,
    "Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia|not_provided": 1,
    "not_provided|Ca/Tu_ALLOANTIGEN_POLYMORPHISM|Glanzmann_thrombasthenia": 1,
    "not_provided|ITGB3-related_disorder|not_specified": 1,
    "ITGB3-related_disorder|not_provided|not_specified": 1,
    "Glanzmann_thrombasthenia|Platelet-type_bleeding_disorder_16|Abnormal_bleeding|Prolonged_bleeding_time": 1,
    "not_specified|ITGB3-related_disorder|not_provided": 2,
    "Bleeding_disorder|_platelet-type|_24|Glanzmann_thrombasthenia": 1,
    "not_provided|ITGB3-related_disorder|Glanzmann_thrombasthenia": 1,
    "Glanzmann_thrombasthenia|not_provided|not_specified": 2,
    "ITGB3-related_disorder|not_provided|Glanzmann_thrombasthenia|Platelet-type_bleeding_disorder_16": 1,
    "Thrombocytopenia|Increased_mean_platelet_volume": 1,
    "Glanzmann_thrombasthenia|ITGB3-related_disorder|Glanzmann_thrombasthenia_2|not_provided": 1,
    "Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|not_provided|Glanzmann_thrombasthenia|not_specified": 1,
    "Bleeding_disorder|_platelet-type|_24|not_provided": 2,
    "not_provided|Bleeding_disorder|_platelet-type|_24": 1,
    "not_provided|Abnormal_platelet_aggregation|Thrombocytopenia": 1,
    "Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_1|not_provided|Platelet-type_bleeding_disorder_16|Hyper-IgE_recurrent_infection_syndrome_1|_autosomal_dominant|Glanzmann_thrombasthenia": 1,
    "not_provided|Inborn_genetic_diseases|Bleeding_disorder|_platelet-type|_24": 1,
    "Myocardial_infarction|_susceptibility_to|Glanzmann_thrombasthenia_2|Bleeding_disorder|_platelet-type|_24|not_provided": 1,
    "EFCAB13-related_disorder": 25,
    "not_specified|EFCAB13-related_disorder": 1,
    "Asthma|_aspirin-induced|_susceptibility_to|Asthma_and_nasal_polyps|Immunodeficiency_88": 1,
    "Immunodeficiency_88|Asthma|_nasal_polyps|_and_aspirin_intolerance": 2,
    "Asthma|_nasal_polyps|_and_aspirin_intolerance|Immunodeficiency_88|not_specified": 2,
    "Asthma|_nasal_polyps|_and_aspirin_intolerance|Immunodeficiency_88": 1,
    "not_provided|Immunodeficiency_88|not_specified": 1,
    "TBX21-related_disorder": 4,
    "Immunodeficiency_88": 1,
    "Immunodeficiency_88|Asthma|_nasal_polyps|_and_aspirin_intolerance|not_provided": 1,
    "MRPL10-related_disorder": 3,
    "Amelogenesis_imperfecta|_IIa_1K|Amelogenesis_imperfecta": 1,
    "Amelogenesis_imperfecta|_IIa_1K": 1,
    "Pyridoxal_phosphate-responsive_seizures": 259,
    "Pyridoxal_phosphate-responsive_seizures|not_provided": 12,
    "not_provided|Pyridoxal_phosphate-responsive_seizures|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Pyridoxal_phosphate-responsive_seizures": 4,
    "not_provided|Pyridoxal_phosphate-responsive_seizures": 27,
    "Inborn_genetic_diseases|Pyridoxal_phosphate-responsive_seizures|not_provided": 4,
    "Pyridoxal_phosphate-responsive_seizures|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Pyridoxal_phosphate-responsive_seizures": 5,
    "Pyridoxal_phosphate-responsive_seizures|not_specified": 5,
    "not_specified|Pyridoxal_phosphate-responsive_seizures": 5,
    "PNPO-related_disorder|Pyridoxal_phosphate-responsive_seizures": 2,
    "Inborn_genetic_diseases|not_specified|Pyridoxal_phosphate-responsive_seizures": 2,
    "not_provided|Pyridoxal_phosphate-responsive_seizures|not_specified": 2,
    "not_provided|not_specified|Pyridoxal_phosphate-responsive_seizures|Inborn_genetic_diseases": 1,
    "PNPO-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Pyridoxal_phosphate-responsive_seizures|not_provided": 2,
    "not_specified|Pyridoxal_phosphate-responsive_seizures|Inborn_genetic_diseases|not_provided": 2,
    "PNPO-related_disorder|Inborn_genetic_diseases|not_provided|Pyridoxal_phosphate-responsive_seizures": 1,
    "Pyridoxal_phosphate-responsive_seizures|not_specified|not_provided": 1,
    "PNPO-related_disorder|not_provided|Pyridoxal_phosphate-responsive_seizures": 1,
    "not_provided|Pyridoxal_phosphate-responsive_seizures|Neuronopathy|_distal_hereditary_motor|_type_5A|Fetal_growth_restriction|Growth_delay|Seizure": 1,
    "not_provided|PNPO-related_disorder|Pyridoxal_phosphate-responsive_seizures": 1,
    "Pyridoxal_phosphate-responsive_seizures|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Pyridoxal_phosphate-responsive_seizures": 1,
    "PNPO-related_disorder|not_specified|not_provided|Pyridoxal_phosphate-responsive_seizures": 1,
    "Pyridoxal_phosphate-responsive_seizures|Inborn_genetic_diseases|not_provided": 1,
    "Pulmonary_hypoplasia": 1,
    "Facial_paresis|_hereditary_congenital|_3|not_specified|not_provided": 1,
    "Facial_paresis|_hereditary_congenital|_3": 4,
    "HOXB1-related_disorder": 2,
    "HOXB1-related_disorder|not_provided": 1,
    "not_provided|Facial_paresis|_hereditary_congenital|_3|HOXB1-related_disorder": 1,
    "Meckel_syndrome|_type_1": 40,
    "HOXB6-related_disorder": 3,
    "Prostate_cancer|_hereditary|_9|not_provided": 18,
    "Prostate_cancer|_hereditary|_9": 39,
    "Hereditary_cancer-predisposing_syndrome|not_specified|HOXB13-related_disorder|not_provided|Prostate_cancer|_hereditary|_9": 1,
    "not_provided|HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9": 2,
    "Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_provided": 53,
    "Prostate_cancer|_hereditary|_9|not_provided|Hereditary_cancer-predisposing_syndrome": 20,
    "HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Prostate_cancer|_hereditary|_9|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|HOXB13-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9|not_provided": 18,
    "not_provided|HOXB13-related_disorder|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Prostate_cancer|_hereditary|_9": 23,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Prostate_cancer|_hereditary|_1": 10,
    "HOXB13-related_disorder|Prostate_cancer|_hereditary|_9|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome": 20,
    "Hereditary_cancer-predisposing_syndrome|not_provided|HOXB13-related_disorder|Prostate_cancer|_hereditary|_9": 2,
    "Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_provided|Prostate_cancer|_hereditary|_1": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "not_provided|Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9": 1,
    "HOXB13-related_disorder|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9": 3,
    "not_provided|Prostate_cancer|_hereditary|_9": 20,
    "Hereditary_cancer-predisposing_syndrome|not_provided|HOXB13-related_disorder": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9": 16,
    "not_provided|Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome": 12,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9|not_provided|HOXB13-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|HOXB13-related_disorder|not_provided|Prostate_cancer|_hereditary|_9": 1,
    "Hereditary_cancer-predisposing_syndrome|HOXB13-related_disorder|not_provided": 3,
    "HOXB13-related_disorder": 3,
    "not_provided|HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "Prostate_cancer|_hereditary|_1|not_provided|Hereditary_cancer-predisposing_syndrome": 12,
    "HOXB13-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9": 7,
    "Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Prostate_cancer|_hereditary|_9": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|not_provided": 1,
    "Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome": 7,
    "HOXB13-related_disorder|not_provided|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|Prostate_cancer|_hereditary|_9": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9|not_provided": 1,
    "Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9|not_provided": 3,
    "not_provided|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "HOXB13-related_disorder|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|HOXB13-related_disorder|not_provided|not_specified|Prostate_cancer|_hereditary|_9": 1,
    "Prostate_cancer|_hereditary|_9|not_specified|not_provided|HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|HOXB13-related_disorder": 1,
    "not_specified|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9|not_provided": 1,
    "HOXB13-related_disorder|not_provided": 1,
    "HOXB13-related_disorder|HOXB13-Related_Cancer_Predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Prostate_cancer|_hereditary|_9|not_provided|Carcinoma_of_pancreas|Prostate_cancer_susceptibility": 1,
    "not_provided|Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|HOXB13-related_disorder|Prostate_cancer|_hereditary|_9|not_specified": 1,
    "not_provided|Prostate_cancer|_hereditary|_1|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9": 1,
    "Prostate_cancer|_hereditary|_9|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Prostate_cancer|_hereditary|_1|HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|Prostate_cancer|_hereditary|_9|not_provided|HOXB13-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Prostate_cancer|_hereditary|_1|not_provided|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_9": 1,
    "Hereditary_cancer-predisposing_syndrome|HOXB13-related_disorder|Prostate_cancer|_hereditary|_9|not_provided": 1,
    "Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|_hereditary|_1": 1,
    "not_provided|not_specified|Prostate_cancer|_hereditary|_9|Hereditary_cancer-predisposing_syndrome": 1,
    "SNF8-associated_disease|Neurodevelopmental_disorder_plus_optic_atrophy": 2,
    "SNF8-associated_disease|Developmental_and_epileptic_encephalopathy_115": 1,
    "SNF8-associated_disease|Developmental_and_epileptic_encephalopathy_115|SNF8-associated_disorder": 2,
    "not_specified|SNF8-associated_disease|Neurodevelopmental_disorder_plus_optic_atrophy": 1,
    "Developmental_and_epileptic_encephalopathy_115|Neurodevelopmental_disorder_plus_optic_atrophy|SNF8-associated_disease": 1,
    "BLOOD_GROUP|_SID_SYSTEM|not_provided": 3,
    "BLOOD_GROUP|_SID_SYSTEM": 1,
    "Early-onset_dementia_of_unclear_type": 1,
    "PHB1-related_disorder": 2,
    "Neurodevelopmental_disorder_with_microcephaly_and_dysmorphic_facies": 6,
    "SPOP-related_disorder": 3,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_relative_macrocephaly_and_with_or_without_cardiac_or_endocrine_anomalies|Neurodevelopmental_disorder_with_microcephaly_and_dysmorphic_facies": 1,
    "Neurodevelopmental_disorder_with_microcephaly_and_dysmorphic_facies|Prostate_cancer|not_provided": 1,
    "Nabais_Sa-de_Vries_syndrome": 1,
    "Neurodevelopmental_disorder_with_relative_macrocephaly_and_with_or_without_cardiac_or_endocrine_anomalies|Neurodevelopmental_disorder_with_microcephaly_and_dysmorphic_facies": 1,
    "not_provided|Neurodevelopmental_disorder_with_relative_macrocephaly_and_with_or_without_cardiac_or_endocrine_anomalies": 2,
    "Neurodevelopmental_disorder_with_relative_macrocephaly_and_with_or_without_cardiac_or_endocrine_anomalies": 3,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_microcephaly_and_dysmorphic_facies": 1,
    "Neurodevelopmental_disorder_with_relative_macrocephaly_and_with_or_without_cardiac_or_endocrine_anomalies|Prostate_cancer|not_provided": 1,
    "SPOP-related_neurodevelopmental_condition|not_provided": 1,
    "SPOP-related_disorder|Neurodevelopmental_disorder_with_relative_macrocephaly_and_with_or_without_cardiac_or_endocrine_anomalies": 1,
    "SLC35B1-related_disorder": 2,
    "DLX4-related_disorder": 7,
    "not_provided|Orofacial_cleft_15": 1,
    "not_provided|DLX4-related_disorder": 1,
    "DLX4-related_disorder|not_specified": 1,
    "Orofacial_cleft_15": 1,
    "Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 47,
    "Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|not_provided": 10,
    "not_provided|Amelogenesis_Imperfecta|_Dominant": 2,
    "Inborn_genetic_diseases|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 2,
    "not_specified|not_provided|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|DLX3-related_disorder": 1,
    "not_provided|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|DLX3-related_disorder": 1,
    "DLX3-related_disorder|not_provided|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 1,
    "not_specified|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|not_provided": 1,
    "Amelogenesis_imperfecta|Peripheral_pulmonary_artery_stenosis|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 1,
    "Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|Tricho-dento-osseous_syndrome": 2,
    "DLX3-related_disorder|Tricho-dento-osseous_syndrome|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|not_provided": 1,
    "not_provided|Tricho-dento-osseous_syndrome|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 2,
    "DLX3-related_disorder": 1,
    "Tricho-dento-osseous_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Tricho-dento-osseous_syndrome|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|not_specified": 1,
    "Tricho-dento-osseous_syndrome": 1,
    "not_provided|DLX3-related_disorder": 1,
    "Uterine_leiomyoma|Tricho-dento-osseous_syndrome": 1,
    "Amelogenesis_Imperfecta|_Dominant|not_provided": 1,
    "not_provided|not_specified|Tricho-dento-osseous_syndrome|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 1,
    "not_provided|not_specified|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 1,
    "Inborn_genetic_diseases|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism|not_provided": 1,
    "not_provided|Hypomaturation-hypoplastic_amelogenesis_imperfecta_with_taurodontism": 1,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 104,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|not_provided": 28,
    "ITGA3-related_disorder": 15,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 2,
    "not_provided|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 14,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|ITGA3-related_disorder|not_provided": 3,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|Inborn_genetic_diseases": 13,
    "Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|not_provided": 3,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "ITGA3-related_disorder|not_provided": 7,
    "not_specified|ITGA3-related_disorder": 1,
    "not_provided|ITGA3-related_disorder|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 1,
    "not_specified|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|not_provided": 1,
    "not_provided|ITGA3-related_disorder": 4,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|not_provided|ITGA3-related_disorder": 1,
    "Bronchopulmonary_dysplasia_of_newborn|Eczematoid_dermatitis|Phimosis|Gastroesophageal_reflux|Respiratory_failure|Penoscrotal_transposition|Feeding_difficulties|Anemia|Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 1,
    "not_provided|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|ITGA3-related_disorder": 1,
    "Nephrotic_syndrome|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 1,
    "ITGA3-related_disorder|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 1,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|ITGA3-related_disorder": 1,
    "Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "ITGA3-related_disorder|not_provided|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_7|_with_interstitial_lung_disease_and_nephrotic_syndrome": 1,
    "SAMD14-related_disorder|not_specified": 1,
    "SAMD14-related_disorder": 6,
    "not_specified|SAMD14-related_disorder": 2,
    "PPP1R9B-related_disorder": 16,
    "not_provided|PPP1R9B-related_disorder": 1,
    "Sarcoglycanopathy|not_specified": 1,
    "SGCA-related_disorder": 2,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided|SGCA-related_disorder|Dystrophin_deficiency|not_specified": 1,
    "Sarcoglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 4,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 537,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 41,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 31,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|SGCA-related_disorder": 3,
    "not_provided|SGCA-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified": 5,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 3,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided|SGCA-related_disorder|Sarcoglycanopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Autosomal_recessive_limb-girdle_muscular_dystrophy": 2,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Autosomal_recessive_limb-girdle_muscular_dystrophy": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 6,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 11,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 3,
    "not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 1,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Abnormality_of_the_musculature": 1,
    "SGCA-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Abnormality_of_the_musculature|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified": 3,
    "Muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified|Sarcoglycanopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Abnormality_of_the_musculature": 2,
    "Sarcoglycanopathy|SGCA-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Hypertrophic_cardiomyopathy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Inborn_genetic_diseases": 5,
    "not_provided|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided|SGCA-related_disorder": 2,
    "Sarcoglycanopathy|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 4,
    "Proximal_muscle_weakness|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "not_specified|not_provided|Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided|not_specified": 1,
    "not_provided|Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Abnormality_of_the_musculature": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|SGCA-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Sarcoglycanopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 2,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|See_cases": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|SGCA-related_disorder": 2,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Qualitative_or_quantitative_defects_of_alpha-sarcoglycan|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Sarcoglycanopathy": 2,
    "Sarcoglycanopathy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Dystrophin_deficiency|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Elevated_circulating_creatine_kinase_concentration": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 1,
    "SGCA-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Sarcoglycanopathy|Inborn_genetic_diseases|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|not_provided": 1,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_specified|not_provided|Cardiomyopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D|Inborn_genetic_diseases": 1,
    "SGCA-related_disorder|Sarcoglycanopathy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2D": 1,
    "Sarcoglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome_type_7A|Osteogenesis_Imperfecta|_Dominant": 17,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis": 6,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 11,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta": 2,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Infantile_cortical_hyperostosis": 3,
    "Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 9,
    "not_provided|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome_type_7A|Osteogenesis_Imperfecta|_Dominant|not_provided": 2,
    "Osteogenesis_imperfecta|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 4,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta": 3,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|not_provided|Osteogenesis_imperfecta": 1,
    "COL1A1-related_disorder": 40,
    "Osteogenesis_Imperfecta|_Dominant|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome_type_7A|Infantile_cortical_hyperostosis|COL1A1-related_disorder": 1,
    "Infantile_cortical_hyperostosis|COL1A1-related_disorder|Ehlers-Danlos_syndrome_type_7A|Osteogenesis_Imperfecta|_Dominant": 1,
    "Ehlers-Danlos_syndrome_type_7A|Infantile_cortical_hyperostosis|Osteogenesis_Imperfecta|_Dominant": 1,
    "not_provided|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type": 7,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I": 5,
    "Cardiovascular_phenotype|COL1A1-related_disorder|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype": 8,
    "not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 61,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 69,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|COL1A1-related_disorder": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder": 11,
    "not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 2,
    "not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 8,
    "Cardiovascular_phenotype|not_provided|not_specified|Osteogenesis_imperfecta_type_I": 2,
    "Osteogenesis_imperfecta_type_I|not_provided": 98,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 13,
    "not_specified|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I": 2,
    "not_provided|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Infantile_cortical_hyperostosis|not_provided|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I": 19,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|COL1A1-related_disorder": 2,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I": 4,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I": 19,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|not_provided|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|not_specified": 3,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_provided|Osteogenesis_imperfecta_type_I|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|Osteogenesis_imperfecta_type_I": 25,
    "Cardiovascular_phenotype|not_provided|COL1A1-related_disorder|not_specified|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|COL1A1-related_disorder|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 4,
    "Osteogenesis_imperfecta_type_I|not_specified|COL1A1-related_disorder|Cardiovascular_phenotype": 1,
    "COL1A1-related_disorder|not_provided": 4,
    "Cardiovascular_phenotype|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_cardiac_valvular_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 2,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Cardiovascular_phenotype": 3,
    "COL1A1-related_disorder|Connective_tissue_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|not_specified|Osteogenesis_imperfecta_type_I": 1,
    "Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta_type_I": 2,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_type_I": 2,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_specified|Ehlers-Danlos_syndrome|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 14,
    "Cardiovascular_phenotype|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Ehlers-Danlos_syndrome|_classic_type|_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 12,
    "Osteogenesis_imperfecta_type_I|not_provided|COL1A1-related_disorder|Cardiovascular_phenotype": 3,
    "Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome": 1,
    "Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|Cardiovascular_phenotype": 4,
    "Osteogenesis_imperfecta_type_2|_thin-bone": 1,
    "Osteogenesis_imperfecta_type_I|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Ehlers-Danlos_syndrome|Infantile_cortical_hyperostosis|not_specified|Cardiovascular_phenotype": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 2,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|not_provided": 7,
    "not_specified|Osteogenesis_imperfecta_type_I|not_provided": 3,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 19,
    "not_provided|COL1A1-related_disorder": 2,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III": 2,
    "Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|not_provided": 4,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 5,
    "not_provided|COL1A1-related_disorder|Cardiovascular_phenotype|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis": 1,
    "Infantile_cortical_hyperostosis": 9,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Hypertrophic_cardiomyopathy|COL1A1-related_disorder|Cardiovascular_phenotype|Keratoconus|not_specified|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|not_specified|Osteogenesis_imperfecta|not_provided|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Cardiovascular_phenotype|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_specified|Cardiovascular_phenotype": 4,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|not_specified|Osteogenesis_imperfecta_type_I": 3,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I": 3,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "Cardiovascular_phenotype|not_provided|Infantile_cortical_hyperostosis|Connective_tissue_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|not_specified": 29,
    "Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "OSTEOGENESIS_IMPERFECTA|_TYPE_IIC": 1,
    "Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_type_III|not_provided": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided|not_specified|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|See_cases": 1,
    "Ehlers-Danlos_syndrome|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis": 1,
    "Infantile_cortical_hyperostosis|not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Abnormality_of_the_skeletal_system": 1,
    "Cardiovascular_phenotype|COL1A1-related_disorder|not_specified|not_provided|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteoporosis|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|not_specified|Osteogenesis_imperfecta|not_provided|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Ehlers-Danlos_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteoporosis": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Cardiovascular_phenotype|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Prostate_cancer|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Ehlers-Danlos_syndrome|not_provided": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_I": 3,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|not_specified": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta": 1,
    "COL1A1-related_disorder|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 4,
    "Cardiovascular_phenotype|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Connective_tissue_disorder|Cardiovascular_phenotype|not_specified|Ehlers-Danlos_syndrome": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|COL1A1-related_disorder|Cardiovascular_phenotype|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Ehlers-Danlos_syndrome": 1,
    "COL1A1-related_disorder|not_provided|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_specified|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_type_I|not_specified|not_provided": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|not_provided|not_specified": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_specified|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Postmenopausal_osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Reduced_bone_mineral_density|Joint_hypermobility": 1,
    "COL1A1-related_disorder|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "COL1A1-related_disorder|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I": 2,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|COL1A1-related_disorder|not_specified|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|not_specified": 5,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_provided|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided": 3,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome": 1,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|COL1A1-related_disorder|Abnormality_of_the_skeletal_system": 1,
    "not_provided|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_III": 1,
    "Osteogenesis_imperfecta_type_I|not_specified|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|COL1A1-related_disorder": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|COL1A1-related_disorder|not_provided": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Postmenopausal_osteoporosis|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta": 2,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder|not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|Ehlers-Danlos_syndrome|Infantile_cortical_hyperostosis|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|not_provided": 2,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis": 2,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided": 1,
    "Ehlers-Danlos_syndrome|_classic_type|_1|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|See_cases|Cardiovascular_phenotype|not_provided": 1,
    "Osteogenesis_imperfecta|not_provided|Osteogenesis_imperfecta_type_I": 2,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_specified|not_provided|COL1A1-related_disorder": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|not_specified|Osteogenesis_imperfecta_type_I|not_provided|Infantile_cortical_hyperostosis": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|not_specified|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome": 2,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Osteoporosis|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_type_III|not_provided|Osteogenesis_imperfecta_type_I|See_cases": 1,
    "Cardiovascular_phenotype|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|not_provided|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_specified|not_provided": 2,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I": 3,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_III": 2,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|COL1A1-related_disorder|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|COL1A1-related_disorder": 2,
    "COL1A1-related_disorder|Osteogenesis_imperfecta|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta|not_provided|not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome": 1,
    "not_provided|COL1A1-related_disorder|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Infantile_cortical_hyperostosis": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided": 1,
    "Osteogenesis_imperfecta|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Osteogenesis_imperfecta_type_I|See_cases": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Ehlers-Danlos_syndrome": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|not_specified": 3,
    "not_specified|Osteogenesis_imperfecta_type_I|Connective_tissue_disorder": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 2,
    "Osteogenesis_imperfecta|not_specified|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Cardiovascular_phenotype": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Cardiovascular_phenotype|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|not_provided|COL1A1-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|COL1A1-related_disorder|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "Cardiovascular_phenotype|not_provided|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|not_provided|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta_type_III": 2,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Osteoporosis|not_provided|Postmenopausal_osteoporosis": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|COL1A1-related_disorder": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|COL1A1-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|not_provided|Osteogenesis_imperfecta": 1,
    "not_provided|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I": 2,
    "Multiple_epiphyseal_dysplasia_type_1|Osteogenesis_imperfecta|_perinatal_lethal": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "COL1A1-related_disorder|Cardiovascular_phenotype|Connective_tissue_disorder|Ehlers-Danlos/osteogenesis_imperfecta_syndrome|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "COL1A1-related_disorder|Ehlers-Danlos_syndrome": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_provided": 3,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|COL1A1-related_disorder|not_specified|Ehlers-Danlos_syndrome|Infantile_cortical_hyperostosis": 1,
    "Ehlers-Danlos_syndrome|not_provided|not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|not_specified|Cardiovascular_phenotype|COL1A1-related_disorder": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Cardiovascular_phenotype|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta|not_specified|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|not_provided": 1,
    "Osteogenesis_imperfecta|not_specified|COL1A1-related_disorder|Ehlers-Danlos_syndrome|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Infantile_cortical_hyperostosis": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Cardiovascular_phenotype|not_provided|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|not_specified": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_type_III/IV": 1,
    "Craniofacial_disproportion|Decreased_calvarial_ossification|Crumpled_long_bones|Bowing_of_limbs_due_to_multiple_fractures|Recurrent_long_bone_fractures|Skeletal_dysplasia|Hypertelorism|Rhizomelia|Neonatal_short-limb_short_stature|Maternal_hypertension|Wide_cranial_sutures|Neonatal_asphyxia|Generalized_hypotonia|Osteopenia|Low-set|_posteriorly_rotated_ears|Wide_anterior_fontanel|Downslanted_palpebral_fissures|Flat_occiput|Premature_birth|Triangular_face|Abnormal_pinna_morphology|Anteverted_nares|Blue_sclerae|Broad_forehead|Depressed_nasal_bridge|Pathologic_fracture|Cranial_asymmetry|not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Abnormality_of_the_skeletal_system": 1,
    "Osteogenesis_imperfecta_type_I|See_cases|not_provided|not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III": 1,
    "Ehlers-Danlos_syndrome|COL1A1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|COL1A1-related_disorder|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Postmenopausal_osteoporosis": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III": 1,
    "COL1A1-related_disorder|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I": 3,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_III|Osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Osteoporosis": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Cardiovascular_phenotype|not_specified|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_specified": 1,
    "Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III": 1,
    "Osteogenesis_imperfecta_type_I|Connective_tissue_disorder": 2,
    "not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Infantile_cortical_hyperostosis|Osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided": 1,
    "Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|not_provided|Ehlers-Danlos_syndrome|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_specified|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Osteogenesis_imperfecta": 1,
    "COL1A1-related_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Infantile_cortical_hyperostosis|Osteoporosis|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "not_provided|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|not_specified|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome": 1,
    "not_specified|Infantile_cortical_hyperostosis|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Cardiovascular_phenotype|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "COL1A1-related_disorder|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|not_specified|Cardiovascular_phenotype|Infantile_cortical_hyperostosis": 1,
    "not_provided|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Cardiovascular_phenotype": 1,
    "Osteoporosis|Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided": 1,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|not_specified|Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "See_cases|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_III|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta|_perinatal_lethal|not_provided|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided": 1,
    "not_provided|Connective_tissue_disorder|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteoporosis|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder": 3,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_specified|not_provided|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Ehlers-Danlos_syndrome|not_provided|Infantile_cortical_hyperostosis|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|COL1A1-related_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I": 1,
    "COL1A1-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|not_specified|not_provided|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Ehlers-Danlos_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|not_provided|Osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Postmenopausal_osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|not_provided": 1,
    "Ehlers-Danlos_syndrome|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "not_specified|COL1A1-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I": 1,
    "COL1A1-related_Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_III": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Ehlers-Danlos_syndrome": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Ehlers-Danlos_syndrome|_classic_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteoporosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|Bruising_susceptibility|Fragile_skin|Joint_hypermobility|not_provided": 1,
    "Connective_tissue_disorder|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|not_provided": 1,
    "Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|not_specified|not_provided": 1,
    "Osteopenia|Blue_sclerae|Increased_susceptibility_to_fractures|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteoporosis|COL1A1-related_disorder|not_provided|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 1,
    "not_provided|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteoporosis|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta|Infantile_cortical_hyperostosis|not_specified|not_provided": 1,
    "COL1A1-related_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_1|_mild|Osteogenesis_imperfecta_type_I": 2,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Stickler_syndrome_type_2|Ehlers-Danlos_syndrome|_arthrochalasia_type|_2|not_provided": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Infantile_cortical_hyperostosis": 1,
    "not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type": 2,
    "Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Infantile_cortical_hyperostosis": 1,
    "Connective_tissue_disorder|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_specified|not_provided|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Infantile_cortical_hyperostosis|Osteoporosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|not_specified|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_type_I|not_provided|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form": 1,
    "Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteoporosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|not_provided|not_specified": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|not_provided|Postmenopausal_osteoporosis": 1,
    "Osteogenesis_imperfecta_type_I|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|Cardiovascular_phenotype|not_provided|COL1A1-related_disorder|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta_type_III|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Cardiovascular_phenotype|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Cardiovascular_phenotype|COL1A1-related_osteogenesis_imperfecta": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta|not_provided": 1,
    "Connective_tissue_disorder|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta_type_I|COL1A1-related_disorder|Congenital_heart_disease": 1,
    "Cardiovascular_phenotype|not_provided|Osteogenesis_imperfecta|COL1A1-related_disorder|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|See_cases|Infantile_cortical_hyperostosis": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Osteogenesis_imperfecta_type_I": 1,
    "Osteogenesis_imperfecta_type_I|not_provided|Ehlers-Danlos_syndrome|not_specified": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|not_specified|not_provided|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|not_specified|not_provided": 1,
    "Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|not_specified|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta|Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided": 1,
    "Cardiovascular_phenotype|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Infantile_cortical_hyperostosis|Osteoporosis|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1": 1,
    "not_provided|Infantile_cortical_hyperostosis|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type": 1,
    "Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I|Ehlers-Danlos_syndrome|_arthrochalasia_type|Infantile_cortical_hyperostosis|Cardiovascular_phenotype|Ehlers-Danlos_syndrome|not_provided|not_specified": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta_type_I": 1,
    "Cardiovascular_phenotype|Ehlers-Danlos_syndrome|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta|not_provided": 1,
    "Ehlers-Danlos_syndrome|_arthrochalasia_type|not_provided|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype": 1,
    "Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "COL1A1-related_disorder|Osteogenesis_imperfecta|Osteogenesis_imperfecta_type_I": 1,
    "Bone_mineral_density_variation_quantitative_trait_locus": 3,
    "Infantile_cortical_hyperostosis|Ehlers-Danlos_syndrome|_arthrochalasia_type|Combined_osteogenesis_imperfecta_and_Ehlers-Danlos_syndrome_1|Osteogenesis_imperfecta|_perinatal_lethal|Osteogenesis_imperfecta_type_III|Osteoporosis|Osteogenesis_imperfecta_with_normal_sclerae|_dominant_form|Osteogenesis_imperfecta_type_I|not_specified|not_provided": 1,
    "not_specified|Ehlers-Danlos_syndrome|_arthrochalasia_type|COL1A1-related_disorder|Cardiovascular_phenotype|not_provided|Ehlers-Danlos_syndrome|Infantile_cortical_hyperostosis|Osteogenesis_imperfecta_type_I|Osteogenesis_imperfecta": 1,
    "Osteogenesis_imperfecta_type_I|Wiedemann-Rautenstrauch-like_progeroid_syndrome|not_provided": 1,
    "not_specified|Osteogenesis_imperfecta_type_I|Cardiovascular_phenotype|COL1A1-related_disorder": 1,
    "Infantile_cortical_hyperostosis|not_provided|Ehlers-Danlos_syndrome|_arthrochalasia_type|Osteogenesis_imperfecta": 1,
    "Global_developmental_delay|Cerebellar_atrophy|Bilateral_squint|Hydrocephalus": 1,
    "Osteogenesis_imperfecta|Spondylo-ocular_syndrome|not_provided": 2,
    "not_provided|XYLT2-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|XYLT2-related_disorder": 9,
    "XYLT2-related_disorder|not_provided": 10,
    "XYLT2-related_disorder|Osteogenesis_imperfecta|not_specified|not_provided": 1,
    "Spondylo-ocular_syndrome|not_provided": 1,
    "not_provided|Spondylo-ocular_syndrome": 3,
    "Osteogenesis_imperfecta|XYLT2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|XYLT2-related_disorder": 1,
    "XYLT2-related_disorder|Osteogenesis_imperfecta|not_provided": 3,
    "Spondylo-ocular_syndrome": 6,
    "not_provided|Osteogenesis_imperfecta|XYLT2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Spondylo-ocular_syndrome": 3,
    "XYLT2-related_disorder": 4,
    "XYLT2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta|not_provided": 1,
    "Spondylo-ocular_syndrome|Osteogenesis_imperfecta|not_provided": 1,
    "not_provided|Osteogenesis_imperfecta|Spondylo-ocular_syndrome": 1,
    "not_provided|Osteogenesis_imperfecta|XYLT2-related_disorder": 2,
    "Autosomal_recessive_inherited_pseudoxanthoma_elasticum|Spondylo-ocular_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Osteogenesis_imperfecta|not_provided|Inborn_genetic_diseases": 1,
    "XYLT2-related_disorder|not_provided|Osteogenesis_imperfecta": 2,
    "not_provided|Inborn_genetic_diseases|XYLT2-related_disorder": 1,
    "Osteogenesis_imperfecta|not_provided|XYLT2-related_disorder": 1,
    "not_provided|Osteogenesis_imperfecta|Spondylo-ocular_syndrome|PSEUDOXANTHOMA_ELASTICUM|_MODIFIER_OF_SEVERITY_OF": 1,
    "CACNA1G-related_disorder": 16,
    "not_provided|CACNA1G-related_disorder": 9,
    "Spinocerebellar_ataxia_type_42": 31,
    "Inborn_genetic_diseases|not_provided|CACNA1G-related_disorder": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_42": 5,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|not_specified|not_provided": 2,
    "not_provided|Spinocerebellar_ataxia_type_42": 7,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42|not_provided": 7,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits": 26,
    "not_provided|Abnormality_of_the_skeletal_system|Hirsutism|Abnormal_facial_shape|Intellectual_disability|_severe": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_42": 2,
    "CACNA1G-related_disorder|not_provided": 17,
    "Inborn_genetic_diseases|CACNA1G-related_disorder|not_provided": 4,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42": 3,
    "not_provided|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42|CACNA1G-related_disorder": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42": 1,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_42": 1,
    "not_provided|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits": 6,
    "Spinocerebellar_ataxia_type_42|Epilepsy|not_provided": 1,
    "Spinocerebellar_ataxia_type_42|not_provided|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_42|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|CACNA1G-related_disorder": 1,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Neurodevelopmental_abnormality|Inborn_genetic_diseases|not_provided": 1,
    "Spinocerebellar_ataxia_type_42|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits": 2,
    "not_provided|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42": 1,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|not_provided": 4,
    "CACNA1G-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42|not_provided": 1,
    "not_provided|Juvenile_myoclonic_epilepsy|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|Spinocerebellar_ataxia_type_42": 1,
    "Vascular_disorder|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_42|not_provided": 4,
    "Hereditary_cerebellar_ataxia": 1,
    "CACNA1G-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|CACNA1G-related_disorder|not_provided": 1,
    "CACNA1G-related_disorder|Spinocerebellar_ataxia_type_42|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|not_provided": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|not_specified": 1,
    "Spinocerebellar_ataxia_42|_early-onset|_severe|_with_neurodevelopmental_deficits|not_provided|CACNA1G-related_disorder": 1,
    "Juvenile_myoclonic_epilepsy|Intellectual_disability": 1,
    "NME1-NME2-related_disorder": 1,
    "not_provided|NME1-NME2-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_23": 7,
    "NOG-related-symphlangism_spectrum_disorder": 1,
    "Proximal_symphalangism_1A": 9,
    "Brachydactyly_type_B2": 2,
    "not_provided|Proximal_symphalangism_1A|Stapes_ankylosis_with_broad_thumbs_and_toes|Brachydactyly_type_B2": 1,
    "not_provided|Proximal_symphalangism_1A|Tarsal-carpal_coalition_syndrome": 2,
    "Stapes_ankylosis_with_broad_thumbs_and_toes": 3,
    "NOG-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "NOG-related_disorder|not_provided": 1,
    "NOG-related_disorder|not_specified|not_provided": 1,
    "NOG-related_disorder": 5,
    "not_provided|Stapes_ankylosis_with_broad_thumbs_and_toes": 1,
    "not_provided|Brachydactyly_type_B2": 1,
    "Brachydactyly_type_B2|Symphalangism-brachydactyly_syndrome|Tarsal-carpal_coalition_syndrome|Stapes_ankylosis_with_broad_thumbs_and_toes|Proximal_symphalangism_1A": 2,
    "Symphalangism-brachydactyly_syndrome|Brachydactyly_type_B2|Tarsal-carpal_coalition_syndrome|Proximal_symphalangism_1A|Stapes_ankylosis_with_broad_thumbs_and_toes|not_provided": 1,
    "Tarsal-carpal_coalition_syndrome": 1,
    "DGKE-related_disorder": 2,
    "Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_7|Atypical_hemolytic-uremic_syndrome": 4,
    "DGKE-related_disorder|not_specified|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Mesangiocapillary_glomerulonephritis|not_provided|Kidney_disorder": 1,
    "Kidney_disorder|not_provided|Mesangiocapillary_glomerulonephritis|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 15,
    "Mesangiocapillary_glomerulonephritis|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 2,
    "not_provided|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 3,
    "Mesangiocapillary_glomerulonephritis|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_provided": 3,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_specified|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_DGKE_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Mesangiocapillary_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 6,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "not_provided|Mesangiocapillary_glomerulonephritis|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "Mesangiocapillary_glomerulonephritis": 3,
    "Atypical_hemolytic-uremic_syndrome|not_provided|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "Atypical_hemolytic-uremic_syndrome|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 2,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Mesangiocapillary_glomerulonephritis": 7,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Mesangiocapillary_glomerulonephritis|Inborn_genetic_diseases": 1,
    "not_specified|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Mesangiocapillary_glomerulonephritis|not_provided": 1,
    "not_provided|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "Nephrotic_syndrome|not_provided|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "not_specified|not_provided|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 2,
    "Inborn_genetic_diseases|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_provided|not_specified": 1,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 2,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_provided|Kidney_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome|Hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|Mesangiocapillary_glomerulonephritis|Hemolytic_uremic_syndrome|_atypical|_susceptibility_to|_7|not_provided|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "Atypical_hemolytic-uremic_syndrome|Mesangiocapillary_glomerulonephritis|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "DGKE-related_disorder|Kidney_disorder|not_provided": 1,
    "Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|not_provided|not_specified": 1,
    "DGKE-related_disorder|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis": 1,
    "DGKE-related_disorder|Immunoglobulin-mediated_membranoproliferative_glomerulonephritis|Mesangiocapillary_glomerulonephritis|not_provided|not_specified": 1,
    "Breast_ductal_adenocarcinoma|not_provided": 1,
    "MRPS23-related_disorder": 2,
    "MRPS23-related_disorder|not_provided": 4,
    "Combined_oxidative_phosphorylation_deficiency_46|Inborn_genetic_diseases|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_46": 1,
    "not_provided|MRPS23-related_disorder": 1,
    "VEZF1-related_disorder": 6,
    "not_provided|not_specified|VEZF1-related_disorder": 1,
    "Cardiomyopathy|_dilated|_100": 1,
    "Intellectual_disability|Neurodevelopmental_delay|Neurodevelopmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 3,
    "Neurodevelopmental_delay|Intellectual_disability|Neurodevelopmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities": 2,
    "not_provided|Intellectual_disability|Neurodevelopmental_delay": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_behavioral_abnormalities|not_provided|Intellectual_disability|Neurodevelopmental_delay": 1,
    "Eosinophil_peroxidase_deficiency": 4,
    "Eosinophil_peroxidase_deficiency|not_provided": 1,
    "not_provided|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 2,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 3,
    "not_provided|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 2,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 3,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|not_provided": 4,
    "MKS1-related_disorder": 57,
    "Bardet-Biedl_syndrome_13|MKS1-related_disorder|Meckel_syndrome|_type_1|not_provided": 1,
    "MKS1-related_disorder|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 1,
    "not_specified|MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 2,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Inborn_genetic_diseases|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 28,
    "Meckel_syndrome|_type_1|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1": 7,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided": 2,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 10,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_1|not_provided|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Peripheral_neuropathy": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|not_provided": 1,
    "not_specified|Bardet-Biedl_syndrome_13|not_provided|Microcephaly|MKS1-related_disorder|Joubert_syndrome_28|Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 2,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder": 14,
    "Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder": 5,
    "Joubert_syndrome_28": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 4,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28": 1,
    "Retinal_dystrophy|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|not_specified": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|MKS1-related_disorder": 2,
    "not_provided|Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 8,
    "MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome": 5,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome": 4,
    "MKS1-related_disorder|Bardet-Biedl_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1": 1,
    "Bardet-Biedl_syndrome_13": 14,
    "not_provided|Meckel_syndrome|_type_1|MKS1-related_disorder|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|not_provided": 1,
    "Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome": 4,
    "Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Hypotonia|Polydactyly|Nystagmus|Joubert_syndrome_28|MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Bardet-Biedl_syndrome": 1,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 18,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_13|not_provided|MKS1-related_disorder|Joubert_syndrome_28|Meckel_syndrome|_type_1": 1,
    "MKS1-related_disorder|not_provided": 2,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28": 13,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|not_provided": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_1|Inborn_genetic_diseases": 1,
    "MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|not_provided": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|MKS1-related_disorder": 1,
    "Joubert_syndrome_28|MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Inborn_genetic_diseases|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 9,
    "Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 4,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|MKS1-related_disorder": 1,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 2,
    "Joubert_syndrome_28|not_specified|MKS1-related_disorder|Optic_atrophy|Retinal_dystrophy|Meckel_syndrome|_type_1|not_provided|Bardet-Biedl_syndrome|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided": 2,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|not_provided|Bardet-Biedl_syndrome_13|Inborn_genetic_diseases|MKS1-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|not_specified|Meckel_syndrome|_type_1|MKS1-related_disorder": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 7,
    "Polycystic_kidney_disease|Multicystic_kidney_dysplasia": 1,
    "MKS1-related_disorder|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 1,
    "not_provided|Retinal_dystrophy|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "MKS1-related_disorder|Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1": 4,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|not_provided|Bardet-Biedl_syndrome_13": 1,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 3,
    "Joubert_syndrome_28|MKS1-related_disorder|not_provided|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|not_provided|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "MKS1-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "MKS1-related_disorder|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 2,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|not_provided": 1,
    "Meckel_syndrome|_type_1|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "MKS1-related_disorder|Inborn_genetic_diseases": 2,
    "Polydactyly|Nystagmus|Hypotonia": 1,
    "Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Inborn_genetic_diseases": 1,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified": 1,
    "MKS1-related_disorder|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_specified|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_1": 1,
    "not_provided|not_specified|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|Inborn_genetic_diseases": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_1": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|Rotary_nystagmus|Global_developmental_delay|Polydactyly|Chronic_kidney_disease|Limb_undergrowth|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "Inborn_genetic_diseases|Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Bardet-Biedl_syndrome_13": 1,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|not_provided": 2,
    "MKS1-related_disorder|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_1|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 5,
    "not_provided|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|not_specified": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|not_provided": 2,
    "not_provided|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|not_provided": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|not_provided": 2,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_1|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|not_specified": 1,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|MKS1-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder": 1,
    "Leber_congenital_amaurosis_6|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "MKS1-related_disorder|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|Inborn_genetic_diseases": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|not_provided": 1,
    "Inborn_genetic_diseases|MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|Meckel_syndrome|_type_1": 1,
    "Joubert_syndrome_and_related_disorders|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "not_specified|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|not_specified": 1,
    "Meckel_syndrome|_type_1|not_specified|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 1,
    "not_provided|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|not_specified|Joubert_syndrome_28|MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 2,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Joubert_syndrome_28": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder|not_provided": 2,
    "Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder": 3,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided": 1,
    "Meckel_syndrome|_type_1|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder|not_specified|not_provided|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|not_specified|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|MKS1-related_disorder|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_13|not_provided|Joubert_syndrome_28": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 2,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome|Bardet-Biedl_syndrome_13|MKS1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1": 1,
    "not_specified|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|not_provided": 1,
    "not_provided|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13": 1,
    "Meckel_syndrome|_type_1|not_provided|Meckel-Gruber_syndrome|Joubert_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|MKS1-related_disorder|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|MKS1-related_disorder|Meckel_syndrome|_type_1": 1,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|not_provided|MKS1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Bardet-Biedl_syndrome_13|not_provided|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder": 1,
    "MKS1-related_disorder|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13": 1,
    "not_specified|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "not_provided|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided": 1,
    "not_provided|MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|MKS1-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel_syndrome|_type_1|MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "not_specified|Meckel_syndrome|_type_1|MKS1-related_disorder|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 1,
    "Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|Optic_atrophy|MKS1-related_disorder": 1,
    "Bardet-Biedl_syndrome_13|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_provided|Meckel_syndrome|_type_1": 1,
    "Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|not_provided": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder|Meckel_syndrome|_type_1|Inborn_genetic_diseases|not_provided": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|MKS1-related_disorder|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|not_provided|Meckel_syndrome|_type_1": 1,
    "MKS1-related_disorder|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Inborn_genetic_diseases|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome|Joubert_syndrome_28|Meckel_syndrome|_type_1": 2,
    "MKS1-related_disorder|not_provided|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1": 1,
    "MKS1-related_disorder|not_provided|not_specified|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "not_provided|MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided": 1,
    "Meckel_syndrome|_type_1|Inborn_genetic_diseases|not_provided|MKS1-related_disorder|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Spastic_ataxia|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|not_provided|not_specified": 1,
    "Meckel_syndrome|_type_1|not_provided|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome|Meckel-Gruber_syndrome": 1,
    "MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13": 1,
    "Joubert_syndrome_28|not_specified|not_provided|Bardet-Biedl_syndrome_13": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|MKS1-related_disorder|Bardet-Biedl_syndrome_13|Joubert_syndrome_28|not_provided": 1,
    "Bardet-Biedl_syndrome_13|Joubert_syndrome_28|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome|MKS1-related_disorder": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|MKS1-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|MKS1-related_disorder": 1,
    "Meckel_syndrome|_type_1|Meckel-Gruber_syndrome|Joubert_syndrome|not_provided|MKS1-related_disorder|Joubert_syndrome_28|Bardet-Biedl_syndrome_13": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|not_specified": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|Meckel-Gruber_syndrome|Joubert_syndrome": 1,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Joubert_syndrome_28": 1,
    "not_provided|MKS1-related_disorder": 2,
    "not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_1": 1,
    "Inborn_genetic_diseases|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-Gruber_syndrome|Joubert_syndrome|MKS1-related_disorder|Meckel_syndrome|_type_1|Joubert_syndrome_28|Bardet-Biedl_syndrome_13|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_1": 1,
    "Meckel_syndrome|_type_1|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome|Bardet-Biedl_syndrome_13": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|not_specified|not_provided|Meckel_syndrome|_type_1": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28|not_provided|Inborn_genetic_diseases|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "MKS1-related_disorder|Joubert_syndrome_28|Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|Inborn_genetic_diseases": 1,
    "MKS1-related_disorder|Bardet-Biedl_syndrome_13|Meckel_syndrome|_type_1|Joubert_syndrome_28": 1,
    "Meckel_syndrome|_type_1|Bardet-Biedl_syndrome_13|not_specified": 1,
    "MKS1-related_disorder|not_provided|not_specified": 1,
    "Myeloperoxidase_deficiency|Alzheimer_disease_type_1|MPO-related_disorder|not_provided": 1,
    "not_specified|Alzheimer_disease_type_1": 1,
    "Alzheimer_disease_type_1|Myeloperoxidase_deficiency|MPO-related_disorder|not_provided|not_specified": 1,
    "MPO-related_disorder|not_specified|not_provided": 1,
    "MPO-related_disorder": 8,
    "Myeloperoxidase_deficiency": 9,
    "Alzheimer_disease_type_1|Myeloperoxidase_deficiency|MPO-related_disorder|not_provided": 1,
    "MPO-related_disorder|not_provided|Myeloperoxidase_deficiency": 2,
    "Myeloperoxidase_deficiency|MPO-related_disorder": 1,
    "not_provided|MPO-related_disorder": 2,
    "not_provided|Myeloperoxidase_deficiency": 2,
    "Myeloperoxidase_deficiency|Alzheimer_disease_type_1": 3,
    "MPO-related_disorder|Myeloperoxidase_deficiency": 1,
    "Myeloperoxidase_deficiency|Alzheimer_disease_type_1|not_provided": 1,
    "not_provided|Myeloperoxidase_deficiency|Alzheimer_disease_type_1": 1,
    "Alzheimer_disease_type_1|Myeloperoxidase_deficiency": 1,
    ".|Lung_cancer|_protection_against|_in_smokers": 1,
    "not_provided|Dystonia_22|_adult-onset": 1,
    "not_specified|TSPOAP1-related_Dystonia|TSPOAP1-related_disorder": 1,
    "Dystonia_22|_adult-onset|Dystonia_22|_juvenile-onset": 1,
    "Dystonia_22|_juvenile-onset": 3,
    "TSPOAP1-related_disorder": 1,
    "TSPOAP1-related_Dystonia": 1,
    "Intellectual_disability|Juvenile-onset_progressive_generalized_dystonia|Cerebellar_atrophy": 1,
    "not_specified|not_provided|Sessile_serrated_polyposis_cancer_syndrome": 6,
    "not_provided|not_specified|Hyperplastic_polyposis_syndrome": 4,
    "Sessile_serrated_polyposis_cancer_syndrome|not_specified|not_provided": 42,
    "Hyperplastic_polyposis_syndrome": 2,
    "Sessile_serrated_polyposis_cancer_syndrome": 48,
    "not_specified|Sessile_serrated_polyposis_cancer_syndrome|not_provided": 12,
    "not_provided|not_specified|RNF43-related_disorder": 1,
    "Sessile_serrated_polyposis_cancer_syndrome|not_provided|not_specified": 20,
    "Sessile_serrated_polyposis_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_provided|RNF43-related_disorder|not_specified": 1,
    "not_provided|not_specified|Sessile_serrated_polyposis_cancer_syndrome": 22,
    "not_provided|Sessile_serrated_polyposis_cancer_syndrome": 11,
    "Sessile_serrated_polyposis_cancer_syndrome|not_specified": 4,
    "not_provided|not_specified|RNF43-related_disorder|Hyperplastic_polyposis_syndrome": 2,
    "Sessile_serrated_polyposis_cancer_syndrome|not_provided|RNF43-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Sessile_serrated_polyposis_cancer_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Sessile_serrated_polyposis_cancer_syndrome|not_provided": 1,
    "Sessile_serrated_polyposis_cancer_syndrome|not_provided": 10,
    "Sessile_serrated_polyposis_cancer_syndrome|not_specified|not_provided|RNF43-related_disorder": 1,
    "Hyperplastic_polyposis_syndrome|not_provided|not_specified": 1,
    "Sessile_serrated_polyposis_cancer_syndrome|Hyperplastic_polyposis_syndrome|not_specified|not_provided": 3,
    "not_specified|Hyperplastic_polyposis_syndrome": 3,
    "not_provided|Sessile_serrated_polyposis_cancer_syndrome|not_specified": 14,
    "not_specified|RNF43-related_disorder|Sessile_serrated_polyposis_cancer_syndrome|not_provided": 1,
    "RNF43-related_disorder|Hyperplastic_polyposis_syndrome|not_specified|not_provided": 2,
    "Hyperplastic_polyposis_syndrome|Sessile_serrated_polyposis_cancer_syndrome|not_provided|not_specified": 1,
    "Sessile_serrated_polyposis_cancer_syndrome|not_provided|Hyperplastic_polyposis_syndrome|not_specified": 1,
    "Hyperplastic_polyposis_syndrome|not_specified|not_provided": 3,
    "not_specified|Hyperplastic_polyposis_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|RNF43-related_disorder|Hyperplastic_polyposis_syndrome|Sessile_serrated_polyposis_cancer_syndrome|not_provided": 1,
    "RNF43-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hyperplastic_polyposis_syndrome|not_provided": 1,
    "not_specified|RNF43-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hyperplastic_polyposis_syndrome": 2,
    "RNF43-related_disorder|not_specified|not_provided": 1,
    "Sessile_serrated_polyposis_cancer_syndrome|Hyperplastic_polyposis_syndrome|not_provided": 1,
    "RNF43-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hyperplastic_polyposis_syndrome|not_provided": 1,
    "not_provided|Hyperplastic_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Sessile_serrated_polyposis_cancer_syndrome": 1,
    "not_provided|RNF43-related_disorder|Hyperplastic_polyposis_syndrome|not_specified": 1,
    "not_specified|not_provided|RNF43-related_disorder|Hereditary_cancer|Hyperplastic_polyposis_syndrome": 1,
    "not_specified|not_provided|RNF43-related_disorder|Sessile_serrated_polyposis_cancer_syndrome": 1,
    "Colon_serrated_polyposis|Sessile_serrated_polyposis_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|RNF43-related_disorder|Hyperplastic_polyposis_syndrome|not_provided": 1,
    "RNF43-related_disorder|not_specified|not_provided|Sessile_serrated_polyposis_cancer_syndrome": 1,
    "TEX14-related_disorder": 15,
    "Spermatogenic_failure_23|not_provided": 1,
    "not_provided|TEX14-related_disorder": 2,
    "Spermatogenic_failure_23": 6,
    "TEX14-related_disorder|not_specified": 1,
    "TEX14-related_disorder|not_provided": 1,
    "not_provided|Spermatogenic_failure_23|Non-obstructive_azoospermia|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "not_provided|Non-obstructive_azoospermia|Spermatogenic_failure_23": 1,
    "Fanconi_anemia_complementation_group_O": 431,
    "Breast_and_Ovarian_Cancer_Susceptibility|Hereditary_cancer-predisposing_syndrome|not_provided|RAD51C-related_disorder|Fanconi_anemia|not_specified": 1,
    "not_specified|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O": 7,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 165,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Gastric_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided": 11,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 44,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 158,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 64,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 42,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 20,
    "Fanconi_anemia_complementation_group_O|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 25,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_provided": 9,
    "not_provided|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 11,
    "Fanconi_anemia_complementation_group_O|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|not_provided|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 37,
    "not_provided|not_specified|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 42,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_O": 3,
    "Childhood_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 48,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O": 8,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 36,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 2,
    "Fanconi_anemia_complementation_group_O|not_provided": 4,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 22,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_cancer": 1,
    "Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Inherited_ovarian_cancer_(without_breast_cancer)": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Fanconi_anemia_complementation_group_O": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Inherited_ovarian_cancer_(without_breast_cancer)|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O": 1,
    "not_provided|Fanconi_anemia_complementation_group_O|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "not_provided|Fanconi_anemia_complementation_group_O": 9,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_O": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 3,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided": 12,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Fanconi_anemia_complementation_group_O": 2,
    "not_specified|Breast_and/or_ovarian_cancer|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "Fanconi_anemia_complementation_group_O|not_specified": 5,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 2,
    "Fanconi_anemia_complementation_group_O|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 5,
    "not_specified|Fanconi_anemia_complementation_group_O": 4,
    "RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|RAD51C-related_disorder|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Malignant_tumor_of_breast": 2,
    "Fanconi_anemia_complementation_group_O|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|RAD51C-related_disorder|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 8,
    "Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Breast_and_Ovarian_Cancer_Susceptibility|not_provided": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Ovarian_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|RAD51C-related_disorder|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "RAD51C-related_disorder|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 5,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Ovarian_neoplasm|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_O|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer|RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|RAD51C-related_disorder": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 3,
    "RAD51C-related_disorder|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 2,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Familial_ovarian_cancer|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_O|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O": 2,
    "RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Ovarian_neoplasm|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "RAD51C-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Inherited_breast_cancer_and_ovarian_cancer|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|not_provided": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "RAD51C-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 4,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_cancer-predisposing_syndrome|Microcephaly|Familial_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "RAD51C-related_disorder|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_ovarian_cancer|RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon|Premature_ovarian_insufficiency": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 6,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 2,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|RAD51C-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_O": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 2,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Endometrial_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "RAD51C-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_neoplasm": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|RAD51C-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Ovarian_neoplasm|Hereditary_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_specified": 2,
    "not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Breast_and/or_ovarian_cancer": 1,
    "RAD51C-related_disorder|Inherited_ovarian_cancer_(without_breast_cancer)|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_O|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 8,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|RAD51C-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Fanconi_anemia_complementation_group_O|Endometrial_carcinoma|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|RAD51C-related_disorder": 1,
    "not_provided|Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 2,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_ovarian_cancer|RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|Long_QT_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Ovarian_neoplasm": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Gastric_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Familial_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified": 1,
    "not_provided|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 3,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|not_specified|Familial_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided": 2,
    "not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Malignant_tumor_of_breast|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Ovarian_neoplasm|Malignant_tumor_of_breast": 1,
    "RAD51C-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Gastric_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_O|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "Ovarian_neoplasm|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 2,
    "RAD51C-related_disorder|Breast_and_Ovarian_Cancer_Susceptibility|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Malignant_tumor_of_breast": 1,
    "RAD51C-related_disorder|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|RAD51C-related_disorder": 1,
    "Familial_ovarian_cancer|RAD51C-related_disorder|Hereditary_site-specific_ovarian_cancer_syndrome|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_O|Breast_carcinoma": 1,
    "Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|RAD51C-related_disorder": 1,
    "RAD51C-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|not_specified|not_provided": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|RAD51C-related_disorder|not_provided": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_specified": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome|Gastric_cancer": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|not_specified": 1,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Familial_ovarian_cancer": 1,
    "Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Uterine_corpus_cancer|Hereditary_site-specific_ovarian_cancer_syndrome|Hereditary_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_O": 1,
    "RAD51C-related_disorder": 1,
    "not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Fanconi_anemia_complementation_group_O|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_specified|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Premature_ovarian_failure|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_O|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Familial_ovarian_cancer|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Fanconi_anemia_complementation_group_O|Breast-ovarian_cancer|_familial|_susceptibility_to|_3": 1,
    "Breast_and/or_ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_3|Fanconi_anemia_complementation_group_O|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Fanconi_anemia|not_specified|Breast_and_Ovarian_Cancer_Susceptibility|not_provided": 1,
    "Mulibrey_nanism_syndrome|not_provided": 33,
    "not_provided|Mulibrey_nanism_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Mulibrey_nanism_syndrome": 2,
    "Inborn_genetic_diseases|Mulibrey_nanism_syndrome": 2,
    "not_specified|TRIM37-related_disorder|not_provided|Mulibrey_nanism_syndrome": 2,
    "not_provided|Mulibrey_nanism_syndrome": 18,
    "TRIM37-related_disorder": 2,
    "not_specified|not_provided|Mulibrey_nanism_syndrome": 2,
    "Mulibrey_nanism_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "See_cases|Mulibrey_nanism_syndrome": 1,
    "Mulibrey_nanism_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|TRIM37-related_disorder": 1,
    "Mulibrey_nanism_syndrome|not_provided|not_specified": 1,
    "Mulibrey_nanism_syndrome|not_specified|not_provided": 1,
    "TRIM37-related_disorder|not_provided": 1,
    "Mulibrey_nanism_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Mulibrey_nanism_syndrome|not_provided": 1,
    "Mulibrey_nanism_syndrome|TRIM37-related_disorder": 1,
    "SMG8-related_disorder|Inborn_genetic_diseases": 1,
    "Alzahrani-Kuwahara_syndrome": 13,
    "Inborn_genetic_diseases|SMG8-related_disorder": 2,
    "SMG8-related_disorder": 5,
    "CLTC-related_disorder|not_provided": 7,
    "Intellectual_disability|_autosomal_dominant_56|not_provided": 9,
    "Intellectual_disability|_autosomal_dominant_56": 71,
    "not_provided|CLTC-related_disorder": 11,
    "CLTC-related_disorder": 11,
    "not_provided|Intellectual_disability|_autosomal_dominant_56": 9,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_56": 1,
    "CLTC-related_disorder|Inborn_genetic_diseases": 1,
    "CLTC-related_disorder|not_specified|not_provided": 1,
    "Autosomal_dominant_non-syndromic_intellectual_disability|Intellectual_disability|_autosomal_dominant_56": 1,
    "Intellectual_disability|_autosomal_dominant_56|Inborn_genetic_diseases": 2,
    "CLTC-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_56": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_56": 1,
    "Intellectual_disability|_autosomal_dominant_56|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_56|Inborn_genetic_diseases": 1,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_1": 3,
    "not_provided|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_1": 2,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_1|not_provided": 1,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_1|Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset|Global_developmental_delay|Cerebellar_ataxia|Hearing_impairment": 1,
    "PTRH2-related_disorder": 1,
    "not_provided|PTRH2-related_disorder": 1,
    "not_provided|PTRH2-related_disorder|not_specified": 1,
    "Polydactyly": 1,
    "CA4-related_disorder|Retinitis_pigmentosa|Retinitis_pigmentosa_17|not_provided": 1,
    "Retinitis_pigmentosa|CA4-related_disorder|not_provided": 2,
    "not_provided|CA4-related_disorder": 3,
    "not_provided|Retinitis_pigmentosa_17|Retinal_dystrophy": 1,
    "not_specified|Retinal_dystrophy|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_17|not_provided": 1,
    "CA4-related_disorder": 1,
    "CA4-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_17": 1,
    "not_provided|Retinitis_pigmentosa_17": 1,
    "CA4-related_disorder|not_provided|not_specified|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|CA4-related_disorder|not_specified|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_17|CA4-related_disorder": 1,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|not_provided": 5,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold": 29,
    "not_provided|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|Hereditary_cancer-predisposing_syndrome": 1,
    "PPM1D-related_disorder|Inborn_genetic_diseases": 2,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|Familial_cancer_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold": 1,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold": 4,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold": 1,
    "PPM1D-related_disorder|not_provided": 1,
    "PPM1D-related_disorder": 2,
    "Familial_cancer_of_breast|not_provided|PPM1D-related_disorder": 1,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|PPM1D-related_disorder|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold": 1,
    "not_provided|PPM1D-related_disorder": 1,
    "Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold|not_provided|Lung_carcinoma|Familial_cancer_of_breast|PPM1D-related_disorder": 1,
    "not_provided|Familial_cancer_of_breast|Intellectual_developmental_disorder_with_gastrointestinal_difficulties_and_high_pain_threshold": 1,
    "Hengel-Maroofian-Schols_syndrome|Global_developmental_delay": 3,
    "Hengel-Maroofian-Schols_syndrome": 4,
    "Global_developmental_delay|Hengel-Maroofian-Schols_syndrome": 2,
    "BCAS3-related_disorder": 2,
    "not_provided|TBX2-related_disorder": 9,
    "Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction|TBX2-related_disorder": 2,
    "Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction": 12,
    "Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction|not_specified": 1,
    "TBX2-related_disorder": 11,
    "TBX2-related_disorder|not_provided": 4,
    "not_specified|Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction": 3,
    "Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction|Inborn_genetic_diseases": 1,
    "Vertebral_anomalies_and_variable_endocrine_and_T-cell_dysfunction|not_provided": 5,
    "not_provided|TBX2-related_disorder|not_specified": 1,
    "TBX4-related_disorder": 6,
    "Coxopodopatellar_syndrome": 46,
    "TBX4-related_disorder|not_provided|Coxopodopatellar_syndrome": 1,
    "Coxopodopatellar_syndrome|not_provided": 11,
    "TBX4-related_disorder|Coxopodopatellar_syndrome": 1,
    "not_provided|not_specified|Coxopodopatellar_syndrome": 1,
    "Coxopodopatellar_syndrome|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_amelia|Coxopodopatellar_syndrome": 1,
    "Coxopodopatellar_syndrome|Pulmonary_hypertension|_primary|_1": 6,
    "not_provided|Coxopodopatellar_syndrome": 17,
    "Primary_pulmonary_hypoplasia": 3,
    "not_provided|Coxopodopatellar_syndrome|not_specified": 1,
    "Pulmonary_hypertension|_primary|_1|Coxopodopatellar_syndrome|Autosomal_recessive_amelia": 1,
    "Abnormality_of_prenatal_development_or_birth|Autosomal_recessive_amelia|Coxopodopatellar_syndrome": 1,
    "Autosomal_recessive_amelia": 1,
    "Inborn_genetic_diseases|not_provided|Coxopodopatellar_syndrome": 2,
    "not_specified|not_provided|Coxopodopatellar_syndrome|Autosomal_recessive_amelia": 1,
    "Autosomal_recessive_amelia|Coxopodopatellar_syndrome|Absence_of_the_sacrum|Aplasia/hypoplasia_involving_bones_of_the_lower_limbs|Pulmonary_hypoplasia|Hydroureter|Hydronephrosis|Hypoplastic_left_heart_syndrome": 1,
    "Coxopodopatellar_syndrome|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease": 1,
    "not_provided|TBX4-related_disorder": 1,
    "not_provided|TBX4-related_disorder|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_hypertension|_primary|_1": 1,
    "TBX4-related_disorder|not_provided": 2,
    "not_provided|TBX4-related_disorder|Coxopodopatellar_syndrome": 3,
    "not_specified|Coxopodopatellar_syndrome|not_provided": 1,
    "Pulmonary_hypertension|_primary|_1|Coxopodopatellar_syndrome|not_provided": 1,
    "Coxopodopatellar_syndrome|Pulmonary_hypertension|_primary|_1|not_provided": 1,
    "not_provided|Coxopodopatellar_syndrome|Pulmonary_hypertension|_primary|_1": 1,
    "Primary_pulmonary_hypoplasia|Coxopodopatellar_syndrome|not_provided|Pulmonary_arterial_hypertension|Pulmonary_hypertension|_primary|_1": 1,
    "not_provided|Pulmonary_arterial_hypertension_associated_with_congenital_heart_disease|Pulmonary_hypertension|_primary|_1": 1,
    "not_provided|TBX4-related_disorder|not_specified|Coxopodopatellar_syndrome": 1,
    "not_specified|not_provided|Coxopodopatellar_syndrome": 1,
    "Fanconi_anemia_complementation_group_J": 78,
    "not_provided|Fanconi_anemia_complementation_group_J": 6,
    "Fanconi_anemia_complementation_group_J|not_provided": 2,
    "Fanconi_anemia|Breast_neoplasm": 7,
    "Breast_neoplasm|Fanconi_anemia": 7,
    "Breast_neoplasm|Fanconi_anemia|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|not_provided|not_specified": 1,
    "Breast_neoplasm|Fanconi_anemia|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 908,
    "not_specified|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 410,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 352,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided": 13,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 62,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 301,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided": 35,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 301,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 11,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 19,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 29,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 4,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 8,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 582,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 7,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified": 9,
    "not_specified|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 2,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 33,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome": 14,
    "Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 15,
    "Familial_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Hereditary_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 3,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 113,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 40,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 11,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 8,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 9,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified": 25,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided|BRIP1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_J": 4,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Ovarian_cancer": 1,
    "Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 3,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 18,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Familial_ovarian_cancer|Ovarian_cancer|not_specified": 1,
    "not_provided|Familial_cancer_of_breast|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 8,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided": 36,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Breast_and/or_ovarian_cancer|not_specified|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer": 1,
    "not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 3,
    "Ovarian_cancer|not_provided|Familial_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified": 15,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified": 11,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer": 3,
    "Familial_ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|BRIP1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 6,
    "Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast|not_specified|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|Familial_ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided": 8,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast|not_specified|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided": 10,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 4,
    "Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_cancer": 1,
    "BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 3,
    "Breast_and/or_ovarian_cancer|BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|not_provided|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Inherited_ovarian_cancer_(without_breast_cancer)|not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|not_specified|Ovarian_cancer": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 22,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|not_specified|not_provided": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 13,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|not_specified|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 5,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder|not_provided|not_specified": 1,
    "Gastric_cancer|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer|Ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer": 2,
    "not_specified|Ovarian_cancer|not_provided|BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided|BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Malignant_tumor_of_breast": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Familial_ovarian_cancer": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Breast_cancer|_early-onset|BRIP1-associated_familial_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer": 1,
    "Familial_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 14,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Ovarian_cancer": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified": 12,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 7,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Ovarian_cancer": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified": 8,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|not_specified": 2,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder|not_provided": 1,
    "BRIP1-related_disorder": 3,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "BRIP1-related_disorder|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Inherited_ovarian_cancer_(without_breast_cancer)|Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 10,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Ovarian_cancer|not_specified|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer|not_specified": 1,
    "not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 10,
    "not_provided|Carcinoma_of_pancreas|Ovarian_neoplasm|Familial_ovarian_cancer|BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 7,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer|Hereditary_cancer|not_specified": 1,
    "Familial_ovarian_cancer|BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 4,
    "Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|not_provided|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Neurodevelopmental_delay": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Gastric_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 2,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 5,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|BRIP1-related_disorder|Fanconi_anemia_complementation_group_J": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided": 3,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|Familial_ovarian_cancer|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "BRIP1-related_disorder|Esophageal_atresia/tracheoesophageal_fistula|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Inherited_ovarian_cancer_(without_breast_cancer)|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Fanconi_anemia|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_cancer|_early-onset|Malignant_tumor_of_breast": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided|Ovarian_cancer|Familial_ovarian_cancer|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_ovarian_cancer": 4,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|Breast_and/or_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 4,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder": 3,
    "not_provided|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided|Ovarian_neoplasm|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Gastric_cancer": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided|Breast_carcinoma": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer|Ovarian_cancer|not_specified": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 2,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "Hereditary_cancer|BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided|Ovarian_cancer|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Familial_ovarian_cancer": 2,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|not_specified|not_provided": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 2,
    "Uterine_corpus_cancer|Breast_and/or_ovarian_cancer|Ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Familial_ovarian_cancer|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_skin_disorder|not_provided": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided|Ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 2,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|BRIP1-related_disorder": 1,
    "Breast_neoplasm|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Familial_ovarian_cancer|Fanconi_anemia|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_ovarian_cancer|BRIP1-related_disorder": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "BRIP1-related_disorder|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "BRIP1-associated_familial_cancer_predisposition|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|not_specified|Familial_ovarian_cancer|BRIP1-related_disorder": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|not_provided": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder|Fanconi_anemia_complementation_group_D2|Breast_cancer|_early-onset|not_provided|Ovarian_neoplasm": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Carcinoma_of_colon|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_specified|BRIP1-related_disorder": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|Familial_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|BRIP1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|BRIP1-related_disorder|not_specified|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_cancer|Fanconi_anemia|Breast_neoplasm": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 3,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_ovarian_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast|not_specified": 2,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_specified|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Ovarian_cancer": 2,
    "not_provided|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 2,
    "BRIP1-related_disorder|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Inherited_ovarian_cancer_(without_breast_cancer)|not_specified|not_provided": 1,
    "not_specified|Ovarian_cancer|Familial_ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|BRIP1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome|not_provided": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Familial_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|Gastric_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast|BRIP1-associated_familial_cancer_predisposition|Ovarian_cancer": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 3,
    "not_provided|Ovarian_Cancers|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Malignant_tumor_of_breast|Breast_cancer|_early-onset|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J": 1,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Familial_ovarian_cancer|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 1,
    "Familial_ovarian_cancer|Diffuse_intrinsic_pontine_glioma|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "Ovarian_cancer|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Breast_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Familial_ovarian_cancer|BRIP1-related_disorder|not_specified": 1,
    "Hereditary_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "BRIP1-related_disorder|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided|BRIP1-related_disorder": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Inherited_ovarian_cancer_(without_breast_cancer)|Familial_ovarian_cancer": 1,
    "Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|Ovarian_cancer|not_specified": 1,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Breast_cancer|_early-onset|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Ovarian_cancer": 1,
    "Breast_and/or_ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|BRIP1-related_disorder": 1,
    "Familial_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 2,
    "BRIP1-related_disorder|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast": 1,
    "BRIP1-related_disorder|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRIP1-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Familial_ovarian_cancer|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "not_specified|not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Malignant_tumor_of_breast|Ovarian_cancer|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided|not_specified": 1,
    "Gastric_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|not_specified|not_provided": 1,
    "BRIP1-related_disorder|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|not_provided|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|not_specified|Fanconi_anemia_complementation_group_J": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast": 1,
    "Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Ovarian_cancer": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|Ovarian_cancer": 1,
    "not_specified|Ovarian_cancer|not_provided|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Familial_ovarian_cancer|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Cervical_cancer|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|BRIP1-related_disorder|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided|Ovarian_cancer|not_specified|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|not_specified": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|not_specified": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Breast_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|BRIP1-related_disorder": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer": 1,
    "BRIP1-related_disorder|Gastric_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Ovarian_neoplasm": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_cancer_of_breast|not_specified|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_ovarian_cancer|not_specified|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_ovarian_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder|not_provided|Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J": 1,
    "not_provided|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|Ovarian_cancer": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_provided": 1,
    "BRIP1-related_disorder|Familial_cancer_of_breast|Ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|BRIP1-related_disorder": 1,
    "not_specified|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder": 1,
    "not_specified|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|BRIP1-related_disorder": 1,
    "Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Ovarian_neoplasm|BRIP1-related_disorder|Familial_ovarian_cancer|not_provided|Familial_cancer_of_breast|Ovarian_cancer|not_specified": 1,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|Familial_ovarian_cancer": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Ovarian_cancer|not_provided": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "Ovarian_cancer|Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Fanconi_anemia_complementation_group_J|Ovarian_cancer|Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "not_provided|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|BRIP1-related_disorder": 1,
    "BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified|Familial_ovarian_cancer|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome|not_specified": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Ovarian_neoplasm": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|not_specified|Ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "BRIP1-related_disorder|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_cancer|_early-onset|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|Ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Breast_and/or_ovarian_cancer|Fanconi_anemia_complementation_group_J|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|not_provided|BRIP1-related_disorder|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided|BRIP1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|BRIP1-associated_familial_cancer_predisposition": 1,
    "Ovarian_cancer|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|not_specified|not_provided": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|Familial_cancer_of_breast|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|Fanconi_anemia_complementation_group_J|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Genetic_non-acquired_premature_ovarian_failure|Ovarian_cancer|Fanconi_anemia_complementation_group_J|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|BRIP1-related_disorder": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Fanconi_anemia_complementation_group_J": 1,
    "Hereditary_cancer-predisposing_syndrome|Fanconi_anemia_complementation_group_J|not_provided": 1,
    "INTS2-related_disorder": 3,
    "Intellectual_developmental_disorder_61|Inborn_genetic_diseases": 2,
    "MED13-related_disorder": 32,
    "CDK8-kinase_module-associated_disorder": 1,
    "MED13-related_disorder|not_provided": 9,
    "Inborn_genetic_diseases|See_cases|Intellectual_developmental_disorder_61": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_61": 7,
    "Inborn_genetic_diseases|MED13-related_disorder": 2,
    "not_provided|MED13-related_disorder": 9,
    "Intellectual_developmental_disorder_61|not_provided": 9,
    "MED13-related_disorder|Intellectual_developmental_disorder_61": 2,
    "not_provided|Intellectual_developmental_disorder_61": 2,
    "Intellectual_developmental_disorder_61|MED13-related_disorder": 1,
    "Intellectual_developmental_disorder_61|Intellectual_disability|_autosomal_dominant_13": 1,
    "not_provided|Intellectual_developmental_disorder_61|Inborn_genetic_diseases": 1,
    "MED13-associated_disorder": 1,
    "Autosomal_dominant_isolated_somatotropin_deficiency": 16,
    "not_provided|MED13-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_developmental_disorder_61|MED13-related_disorder": 1,
    "MED13-related_neurodevelopmental_disorder": 1,
    "not_provided|not_specified|MED13-related_disorder": 1,
    "MED13-related_disorder|Inborn_genetic_diseases": 1,
    "MED13-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_57": 13,
    "Intellectual_disability|_autosomal_dominant_57|not_provided": 8,
    "Intellectual_disability|_autosomal_dominant_57": 52,
    "TLK2-related_disorder": 7,
    "TLK2-related_disorder|not_provided": 1,
    "See_cases|TLK2-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_57": 1,
    "Intellectual_disability|_autosomal_dominant_57|TLK2-related_neurodevelopmental_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_57|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_57|not_provided": 1,
    "Intellectual_disability|Intellectual_disability|_autosomal_dominant_57|not_provided": 1,
    "MARCHF10-related_disorder": 26,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 68,
    "TANC2-related_disorder": 29,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|TANC2-related_disorder": 11,
    "not_provided|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 3,
    "INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_AUTISTIC_FEATURES_AND_LANGUAGE_DELAY_WITHOUT_SEIZURES|Autism_spectrum_disorder": 2,
    "TANC2-related_disorder|not_provided": 5,
    "Intellectual_disability|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 1,
    "not_provided|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 1,
    "Inborn_genetic_diseases|TANC2-related_disorder": 1,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_AUTISTIC_FEATURES_AND_LANGUAGE_DELAY_WITHOUT_SEIZURES|Neurodevelopmental_disorder|Autism_spectrum_disorder": 1,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|Inborn_genetic_diseases|not_provided": 1,
    "TANC2-related_neurodevelopmental_disorders": 1,
    "Inborn_genetic_diseases|TANC2-related_disorder|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 1,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|Inborn_genetic_diseases": 4,
    "not_specified|TANC2-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 1,
    "not_provided|Inborn_genetic_diseases|TANC2-related_disorder": 1,
    "See_cases|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures": 3,
    "Developmental_delay|Epilepsy": 1,
    "TANC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_Disability_with_multiple_congenital_anomalies": 1,
    "INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_AUTISTIC_FEATURES_AND_LANGUAGE_DELAY_WITH_SEIZURES|Neurodevelopmental_disorder": 1,
    "INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_AUTISTIC_FEATURES_AND_LANGUAGE_DELAY_WITHOUT_SEIZURES|Neurodevelopmental_disorder": 1,
    "Developmental_delay|Intellectual_disability|INTELLECTUAL_DEVELOPMENTAL_DISORDER_WITH_AUTISTIC_FEATURES_AND_LANGUAGE_DELAY_WITHOUT_SEIZURES": 1,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|TANC2-related_disorder": 2,
    "Intellectual_developmental_disorder_with_autistic_features_and_language_delay|_with_or_without_seizures|not_provided": 1,
    "Abnormality_of_the_musculoskeletal_system": 1,
    "CYB561-related_disorder": 6,
    "Orthostatic_hypotension_2": 2,
    "Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3": 175,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to": 4,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|not_provided|Renal_tubular_dysgenesis": 2,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 8,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|Renal_tubular_dysgenesis|ACE-related_disorder": 1,
    "ACE-related_disorder|Renal_tubular_dysgenesis|not_provided": 6,
    "Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Inborn_genetic_diseases": 2,
    "ACE-related_disorder": 17,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|ACE-related_disorder": 1,
    "not_provided|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin": 11,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Inborn_genetic_diseases": 2,
    "ACE-related_disorder|not_provided|Renal_tubular_dysgenesis": 4,
    "Renal_tubular_dysgenesis|not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "ACE-related_disorder|not_provided": 8,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 3,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|Renal_tubular_dysgenesis": 2,
    "Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|not_provided": 4,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 4,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|not_provided": 10,
    "Renal_tubular_dysgenesis|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "not_provided|ACE-related_disorder": 10,
    "not_provided|ACE-related_disorder|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 4,
    "Renal_tubular_dysgenesis|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 4,
    "Renal_tubular_dysgenesis|not_provided|ACE-related_disorder": 3,
    "Renal_tubular_dysgenesis|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|ACE-related_disorder|not_provided": 1,
    "Renal_tubular_dysgenesis|ACE-related_disorder|not_provided": 2,
    "Renal_tubular_dysgenesis|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 4,
    "Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|not_provided": 4,
    "Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|not_provided|Renal_tubular_dysgenesis|ACE-related_disorder": 2,
    "not_specified|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis|not_provided": 2,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis|not_provided": 3,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3": 4,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis|not_provided": 7,
    "Renal_tubular_dysgenesis|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 1,
    "not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|not_provided|Renal_tubular_dysgenesis": 1,
    "Inborn_genetic_diseases|Renal_tubular_dysgenesis": 1,
    "not_provided|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to": 4,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|Inborn_genetic_diseases": 1,
    "Renal_tubular_dysgenesis|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 1,
    "Hereditary_angioedema_with_normal_C1Inh|not_provided|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3": 1,
    "not_provided|Renal_tubular_dysgenesis|Abnormality_of_prenatal_development_or_birth": 1,
    "ACE-related_disorder|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "Renal_tubular_dysgenesis|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis": 6,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|ACE-related_disorder|not_provided|Renal_tubular_dysgenesis": 1,
    "not_provided|Renal_tubular_dysgenesis|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Inborn_genetic_diseases|ACE-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "not_provided|ACE-related_disorder|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 2,
    "not_provided|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to|Inborn_genetic_diseases": 1,
    "not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 2,
    "not_provided|Renal_tubular_dysgenesis|ACE-related_disorder": 2,
    "not_provided|not_specified|Renal_tubular_dysgenesis": 2,
    "Inborn_genetic_diseases|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "captopril_response_-_Efficacy|Risk_of_requirement_of_invasive_mechanical_ventilation_in_patients_with_severe_COVID-19": 1,
    "Myocardial_infarction|_susceptibility_to|not_specified|Renal_tubular_dysgenesis|not_provided": 1,
    "Microcephaly|not_provided|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin": 2,
    "not_specified|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|not_provided|Renal_tubular_dysgenesis": 1,
    "Inborn_genetic_diseases|Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|not_provided": 1,
    "Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|Renal_tubular_dysgenesis": 1,
    "Hemorrhage|_intracerebral|_susceptibility_to|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|ACE-related_disorder": 1,
    "Inborn_genetic_diseases|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin|ACE-related_disorder": 1,
    "Renal_tubular_dysgenesis_of_genetic_origin|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|not_provided|Inborn_genetic_diseases|Renal_tubular_dysgenesis": 1,
    "Angiotensin_i-converting_enzyme|_benign_serum_increase|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Hemorrhage|_intracerebral|_susceptibility_to|Renal_tubular_dysgenesis_of_genetic_origin": 1,
    "not_specified|not_provided|Renal_tubular_dysgenesis": 3,
    "Inborn_genetic_diseases|Microvascular_complications_of_diabetes|_susceptibility_to|_3|Renal_tubular_dysgenesis_of_genetic_origin|Hemorrhage|_intracerebral|_susceptibility_to": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_8": 8,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_8|not_provided": 3,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_8|not_provided": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_8": 29,
    "not_provided|TACO1-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified|not_provided": 1,
    "TACO1-related_disorder|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_8": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_8|Inborn_genetic_diseases": 1,
    "TACO1-related_disorder": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_8": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_8": 2,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|TACO1-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_8|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "TACO1-related_disorder|not_specified|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_8": 1,
    "TACO1-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_8|not_provided|not_specified": 1,
    "Cerebral_cavernous_malformations_5": 4,
    "MAP3K3-related_disorder": 2,
    "Verrucous_hemangioma|CEREBRAL_CAVERNOUS_MALFORMATIONS_5|_SOMATIC": 1,
    "not_specified|Cerebral_cavernous_malformations_5": 1,
    "Verrucous_hemangioma": 1,
    "Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 327,
    "Inborn_genetic_diseases|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 13,
    "Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|not_provided": 8,
    "Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|not_specified|not_provided": 1,
    "Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|Inborn_genetic_diseases": 13,
    "Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|not_specified": 1,
    "STRADA-related_disorder": 1,
    "intellectual_deficiency|Epilepsy|Polyhydramnios|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 1,
    "not_provided|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 10,
    "Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|STRADA-related_disorder": 1,
    "STRADA-related_disorder|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 5,
    "not_provided|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|STRADA-related_disorder": 2,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 1,
    "STRADA-related_disorder|not_provided|not_specified|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy": 1,
    "not_specified|Polyhydramnios|_megalencephaly|_and_symptomatic_epilepsy|not_provided": 1,
    "CCDC47-related_disorder": 5,
    "Trichohepatoneurodevelopmental_syndrome": 4,
    "Global_developmental_delay_with_dysmorphic_features|_liver_dysfunction|_pruritus|_and_woolly_hair|not_provided|Trichohepatoneurodevelopmental_syndrome": 1,
    "Trichohepatoneurodevelopmental_syndrome|Global_developmental_delay_with_dysmorphic_features|_liver_dysfunction|_pruritus|_and_woolly_hair": 3,
    "not_provided|CCDC47-related_disorder": 1,
    "not_provided|Trichohepatoneurodevelopmental_syndrome": 2,
    "CCDC47-related_disorder|not_provided": 1,
    "PSMC5-related_Neurodevelopmental_proteasomopathy|Neurodevelopmental_disorders|not_provided": 1,
    "PSMC5-related_neurodevelopmental_disorder": 1,
    "not_provided|Specific_granule_deficiency_2|SMARCD2-related_disorder": 2,
    "SMARCD2-related_disorder|not_provided": 6,
    "Specific_granule_deficiency_2": 5,
    "Specific_granule_deficiency_2|Specific_granule_deficiency_1|Autosomal_recessive_severe_congenital_neutropenia": 1,
    "not_provided|SMARCD2-related_disorder": 2,
    "SMARCD2-related_disorder": 4,
    "SMARCD2-related_disorder|Specific_granule_deficiency_2|not_provided": 1,
    "Specific_granule_deficiency_1|Autosomal_recessive_severe_congenital_neutropenia|Specific_granule_deficiency_2": 2,
    "Specific_granule_deficiency_2|Premature_ovarian_insufficiency": 1,
    "GH1-related_disorder": 3,
    "not_provided|Autosomal_dominant_isolated_somatotropin_deficiency": 2,
    "not_specified|not_provided|Decreased_response_to_growth_hormone_stimulation_test": 4,
    "Ateleiotic_dwarfism|Short_stature_due_to_growth_hormone_qualitative_anomaly|Isolated_growth_hormone_deficiency_type_IB|Autosomal_dominant_isolated_somatotropin_deficiency": 2,
    "Ateleiotic_dwarfism": 6,
    "not_provided|Decreased_response_to_growth_hormone_stimulation_test": 6,
    "Decreased_response_to_growth_hormone_stimulation_test|not_provided": 5,
    "Inborn_genetic_diseases|GH1-related_disorder": 1,
    "not_provided|Ateleiotic_dwarfism": 2,
    "Isolated_growth_hormone_deficiency_type_IB|Ateleiotic_dwarfism|Autosomal_dominant_isolated_somatotropin_deficiency|Short_stature_due_to_growth_hormone_qualitative_anomaly|not_provided": 1,
    "Ateleiotic_dwarfism|Isolated_growth_hormone_deficiency_type_IB": 1,
    "GH1-related_disorder|not_provided": 1,
    "Short_stature_due_to_growth_hormone_qualitative_anomaly": 3,
    "not_specified|not_provided|GH1-related_disorder": 1,
    "not_specified|Decreased_response_to_growth_hormone_stimulation_test|Isolated_growth_hormone_deficiency_type_IB|Autosomal_dominant_isolated_somatotropin_deficiency|Ateleiotic_dwarfism|Short_stature_due_to_growth_hormone_qualitative_anomaly": 1,
    "Decreased_response_to_growth_hormone_stimulation_test|not_specified": 1,
    "Idiopathic_growth_hormone_deficiency|Autosomal_dominant_isolated_somatotropin_deficiency": 1,
    "Autosomal_dominant_isolated_somatotropin_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_isolated_somatotropin_deficiency|Ateleiotic_dwarfism|Isolated_growth_hormone_deficiency_type_IB|Short_stature_due_to_growth_hormone_qualitative_anomaly|not_provided": 1,
    "Decreased_response_to_growth_hormone_stimulation_test|Isolated_growth_hormone_deficiency_type_IB": 1,
    "Ateleiotic_dwarfism|not_provided|not_specified": 1,
    "GH1-related_disorder|Autosomal_dominant_isolated_somatotropin_deficiency": 1,
    "Idiopathic_growth_hormone_deficiency|not_provided": 1,
    "not_specified|GH1-related_disorder|not_provided|Autosomal_dominant_isolated_somatotropin_deficiency|Decreased_response_to_growth_hormone_stimulation_test": 1,
    "GH1-related_disorder|Decreased_response_to_growth_hormone_stimulation_test|not_provided|not_specified": 1,
    "not_specified|Decreased_response_to_growth_hormone_stimulation_test|not_provided": 1,
    "Autosomal_dominant_isolated_somatotropin_deficiency|not_provided|Decreased_response_to_growth_hormone_stimulation_test": 1,
    "Isolated_growth_hormone_deficiency_type_IB|Ateleiotic_dwarfism|Autosomal_dominant_isolated_somatotropin_deficiency|Short_stature_due_to_growth_hormone_qualitative_anomaly|not_specified|Decreased_response_to_growth_hormone_stimulation_test|GH1-related_disorder|not_provided": 1,
    "Decreased_response_to_growth_hormone_stimulation_test|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Decreased_response_to_growth_hormone_stimulation_test|not_provided": 1,
    "GH1-related_disorder|not_provided|Decreased_response_to_growth_hormone_stimulation_test": 1,
    "Ateleiotic_dwarfism|not_provided": 1,
    "not_provided|Decreased_response_to_growth_hormone_stimulation_test|not_specified": 1,
    "Decreased_response_to_growth_hormone_stimulation_test|not_specified|GH1-related_disorder|not_provided": 1,
    "not_provided|Isolated_congenital_growth_hormone_deficiency": 1,
    "Isolated_congenital_growth_hormone_deficiency|not_provided": 2,
    "Agammaglobulinemia_6|_autosomal_recessive": 146,
    "Agammaglobulinemia_6|_autosomal_recessive|not_specified": 4,
    "Agammaglobulinemia_6|_autosomal_recessive|CD79B-related_disorder": 2,
    "CD79B-related_disorder|Agammaglobulinemia_6|_autosomal_recessive": 1,
    "not_specified|Agammaglobulinemia_6|_autosomal_recessive": 5,
    "Agammaglobulinemia_6|_autosomal_recessive|not_specified|not_provided": 1,
    "Agammaglobulinemia_6|_autosomal_recessive|not_provided": 3,
    "not_provided|Agammaglobulinemia_6|_autosomal_recessive": 1,
    "not_provided|Agammaglobulinemia_6|_autosomal_recessive|not_specified": 1,
    "Agammaglobulinemia_6|_autosomal_recessive|not_provided|CD79B-related_disorder": 1,
    "CD79B-related_disorder": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 15,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 10,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Congenital_myopathy_22A|_classic": 5,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2": 8,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Congenital_Myasthenic_Syndrome|_Recessive|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|not_provided": 2,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 3,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_provided": 2,
    "Congenital_Myasthenic_Syndrome|_Recessive|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 4,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_Myasthenic_Syndrome|_Recessive|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 7,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Congenital_Myasthenic_Syndrome|_Recessive|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 2,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 2,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided|Congenital_myasthenic_syndrome_16": 1,
    "Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 79,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1": 2,
    "not_specified|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1": 2,
    "Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Inborn_genetic_diseases|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis": 13,
    "not_specified|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 4,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 3,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia": 5,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hyperkalemic_periodic_paralysis|not_provided": 116,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1": 3,
    "SCN4A-related_disorder|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_provided|Limb-girdle_muscular_dystrophy|not_specified": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|not_specified|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 3,
    "Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal": 2,
    "SCN4A-related_disorder|Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Hyperkalemic_periodic_paralysis": 86,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 2,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 16,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16": 1,
    "not_specified|Hyperkalemic_periodic_paralysis": 19,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 2,
    "Paramyotonia_congenita_of_Von_Eulenburg|not_specified|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|not_provided": 5,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 4,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 7,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|not_specified|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|SCN4A-related_disorder|Potassium-aggravated_myotonia": 1,
    "not_provided|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Inborn_genetic_diseases": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia": 4,
    "not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 2,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|not_provided": 2,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 2,
    "Hypokalemic_periodic_paralysis|_type_2": 8,
    "not_provided|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 3,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 6,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_specified|not_provided|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16": 1,
    "Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 2,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_provided|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|SCN4A-related_disorder|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Inborn_genetic_diseases|not_provided|Hyperkalemic_periodic_paralysis": 7,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 2,
    "Inborn_genetic_diseases|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 3,
    "Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "SCN4A-related_non-dystrophic_myotonia": 6,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|not_provided": 2,
    "Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|not_provided": 3,
    "not_provided|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hyperkalemic_periodic_paralysis|not_specified|SCN4A-related_non-dystrophic_myotonia|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 5,
    "SCN4A-related_disorder": 18,
    "not_specified|not_provided|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hyperkalemic_periodic_paralysis|not_specified|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 3,
    "Inborn_genetic_diseases|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16": 1,
    "Hypokalemic_periodic_paralysis|_type_1|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "not_provided|Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "See_cases|Hyperkalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|not_provided|not_specified": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 4,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16": 5,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|not_provided|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Inborn_genetic_diseases|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|not_specified|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 5,
    "Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Skeletal_myopathy|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg": 8,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|not_provided|Paramyotonia_congenita/hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic": 2,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 3,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 3,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "SCN4A-related_disorder|not_specified|not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Tremor|_hereditary_essential|_6|Hyperkalemic_periodic_paralysis": 1,
    "SCN4A-related_disorder|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Long_QT_syndrome": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 6,
    "Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|SCN4A-related_disorder|not_provided": 1,
    "not_provided|SCN4A-related_disorder|Hyperkalemic_periodic_paralysis": 1,
    "not_specified|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis": 2,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 2,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|not_specified": 13,
    "not_provided|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|not_specified|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "SCN4A-related_myopathy|_autosomal_recessive": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 1,
    "not_provided|SCN4A-related_disorder|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|not_specified": 1,
    "Congenital_myasthenic_syndrome_16": 5,
    "not_provided|not_specified|Hyperkalemic_periodic_paralysis": 5,
    "SCN4A-related_non-dystrophic_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia": 1,
    "Acetazolamide-responsive_myotonia|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "Hyperkalemic_periodic_paralysis|SCN4A-related_disorder|not_provided": 3,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 2,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg": 3,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Hyperkalemic_periodic_paralysis": 1,
    "not_specified|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2": 2,
    "Congenital_myopathy_22A|_classic|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|SCN4A-related_non-dystrophic_myotonia|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2": 1,
    "SCN4A-related_non-dystrophic_myotonia|Rhabdomyolysis|SCN4A-related_disorder|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|not_provided|Delayed_gross_motor_development": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 2,
    "Congenital_myasthenic_syndrome|Congenital_myasthenic_syndrome_16": 1,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|not_provided": 4,
    "SCN4A-related_non-dystrophic_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 7,
    "not_specified|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 2,
    "not_specified|Hyperkalemic_periodic_paralysis|not_provided": 3,
    "Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia": 1,
    "Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|not_provided": 4,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Congenital_myopathy_22A|_classic|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|SCN4A-related_disorder|not_provided": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|not_specified": 3,
    "Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Inborn_genetic_diseases|SCN4A-related_disorder": 1,
    "not_specified|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 4,
    "not_specified|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 2,
    "Hyperkalemic_periodic_paralysis|Congenital_myotonia|_autosomal_dominant_form": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 2,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 2,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_specified": 1,
    "SCN4A-related_non-dystrophic_myotonia|SCN4A-related_myopathy|_autosomal_recessive|SCN4A-related_disorder|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "SCN4A-related_non-dystrophic_myotonia|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Myotonia_fluctuans|SCN4A-related_channelopathy|Inborn_genetic_diseases|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Myotonia_permanens|SCN4A-related_myopathy|_autosomal_recessive|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Potassium-aggravated_myotonia": 5,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita/hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "SCN4A-related_disorder|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|not_provided": 2,
    "Hyperkalemic_periodic_paralysis|not_specified|not_provided": 5,
    "SCN4A-related_disorder|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided": 1,
    "Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|not_specified|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "not_specified|not_provided|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_myopathy_22A|_classic|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|not_provided|not_specified": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|SCN4A-related_myopathy|_autosomal_recessive|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_myopathy_22A|_classic|Congenital_myasthenic_syndrome_16|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 2,
    "Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Hyperkalemic_periodic_paralysis|Myotonia_congenita|_atypical|_acetazolamide-responsive": 1,
    "Inborn_genetic_diseases|not_provided|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "SCN4A-related_disorder|Inborn_genetic_diseases|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided|Paramyotonia_congenita/hyperkalemic_periodic_paralysis|Focal-onset_seizure": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|not_provided": 1,
    "Severe_neonatal_hypotonia_improving_with_age|Myopathy": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|not_provided|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Congenital_myopathy_22A|_classic": 1,
    "Skeletal_muscle_channelopathy|not_specified|not_provided|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16": 2,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia": 2,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 2,
    "not_provided|SCN4A-related_disorder|not_specified|Hyperkalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_specified": 3,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|not_provided": 3,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|not_specified|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Inborn_genetic_diseases": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Inborn_genetic_diseases|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_22A|_classic|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "not_specified|Hyperkalemic_periodic_paralysis|not_provided|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|not_specified": 1,
    "not_provided|Limb-girdle_muscular_dystrophy|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|SCN4A-related_disorder|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hyperkalemic_periodic_paralysis|not_specified|SCN4A-related_disorder": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 1,
    "not_specified|not_provided|Hyperkalemic_periodic_paralysis": 3,
    "Congenital_myopathy|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_16": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia": 1,
    "SCN4A-related_disorder|Inborn_genetic_diseases|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_2|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1": 1,
    "not_specified|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|SCN4A-related_myopathy|_autosomal_recessive|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 3,
    "not_provided|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_specified|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|not_specified|not_provided": 2,
    "Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 2,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|not_specified|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 4,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 3,
    "Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "not_provided|Congenital_myasthenic_syndrome_16|not_specified|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|SCN4A-related_non-dystrophic_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16": 1,
    "not_specified|not_provided|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 2,
    "SCN4A-related_disorder|not_specified|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "SCN4A-related_myopathy|_autosomal_recessive|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 2,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|not_provided": 2,
    "not_provided|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Congenital_myasthenic_syndrome_16|not_specified|Paramyotonia_congenita_of_Von_Eulenburg|SCN4A-related_disorder|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "SCN4A-related_disorder|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|not_provided|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_specified": 1,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Congenital_myasthenic_syndrome_16|not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_myopathy_22A|_classic|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "SCN4A-related_disorder|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 2,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 1,
    "Myotonia_fluctuans|not_provided|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita/myotonia_congenita": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22B|_severe_fetal": 2,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|not_provided": 3,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|not_provided|not_specified|Joubert_syndrome_17": 1,
    "Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Congenital_myopathy_22A|_classic|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|not_provided|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|not_provided": 1,
    "not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 2,
    "SCN4A-related_disorder|Hyperkalemic_periodic_paralysis|not_provided": 2,
    "not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 1,
    "Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Sotos_syndrome|SCN4A-related_disorder|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided|Paramyotonia_congenita/hyperkalemic_periodic_paralysis": 1,
    "Handgrip_myotonia|Myotonia|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "SCN4A-related_non-dystrophic_myotonia|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|not_provided|Normokalemic_periodic_paralysis|_potassium-sensitive|Myopathy": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Normokalemic_periodic_paralysis|_potassium-sensitive|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Normokalemic_periodic_paralysis|_potassium-sensitive|Abnormality_of_the_musculature": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Acetazolamide-responsive_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hypokalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2": 1,
    "not_specified|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1": 2,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|SCN4A-related_disorder|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "not_provided|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "not_specified|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|SCN4A-related_disorder|not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Congenital_myopathy_22A|_classic|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "not_provided|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|not_specified": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "not_specified|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|not_provided|not_specified": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 2,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|not_provided|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2": 1,
    "not_specified|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_16": 1,
    "Inborn_genetic_diseases|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_specified": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|SCN4A-related_disorder|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|not_provided|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|not_specified": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Batten-Turner_congenital_myopathy|Pain|EMG:_myotonic_discharges|Limb_pain|Distal_sensory_impairment|Muscle_weakness|Hyperkalemic_periodic_paralysis|Myotonia": 1,
    "SCN4A-related_non-dystrophic_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Neuromuscular_disease|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|SCN4A-related_disorder|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "not_provided|Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_specified|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome_16|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_myopathy_22A|_classic|Inborn_genetic_diseases|not_provided|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|not_specified|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_specified|not_provided|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "not_specified|Congenital_myasthenic_syndrome_16|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "not_provided|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Microcephaly": 1,
    "Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "SCN4A-related_disorder|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|not_provided|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|not_specified|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16": 1,
    "not_specified|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|not_provided|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 2,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|not_specified": 1,
    "Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|See_cases": 1,
    "SCN4A-related_disorder|not_specified|not_provided|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases": 1,
    "Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Inborn_genetic_diseases|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|SCN4A-related_disorder": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|SCN4A-related_disorder": 4,
    "Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Congenital_myasthenic_syndrome|not_specified|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_specified|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|not_specified": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|SCN4A-related_non-dystrophic_myotonia": 1,
    "not_provided|Muscular_channelopathy|Hyperkalemic_periodic_paralysis": 1,
    "SCN4A-related_disorder|Hypokalemic_periodic_paralysis|_type_1|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22B|_severe_fetal": 1,
    "not_provided|Congenital_myopathy_22A|_classic|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal": 1,
    "Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "not_provided|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|not_specified|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "SCN4A-related_myopathy|_autosomal_recessive|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_specified": 1,
    "not_provided|not_specified|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis": 1,
    "Hyperkalemic_periodic_paralysis|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|SCN4A-related_disorder|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|not_provided|not_specified": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Inborn_genetic_diseases|not_provided|SCN4A-related_disorder": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_2|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_provided|not_specified": 1,
    "not_specified|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|not_specified|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|not_provided": 2,
    "Congenital_myasthenic_syndrome_16|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|not_specified|not_provided": 1,
    "not_specified|not_provided|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16": 1,
    "Inborn_genetic_diseases|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Inborn_genetic_diseases|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia": 1,
    "Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal": 1,
    "not_specified|Congenital_myasthenic_syndrome_16|not_provided|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_specified": 1,
    "Inborn_genetic_diseases|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|not_provided": 1,
    "Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Paramyotonia_congenita_of_Von_Eulenburg": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|not_provided|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Hypokalemic_periodic_paralysis|_type_2|Potassium-aggravated_myotonia|Congenital_myasthenic_syndrome_16|Inborn_genetic_diseases": 1,
    "Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_1|Congenital_myasthenic_syndrome_16|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|not_provided": 1,
    "Hyperkalemic_periodic_paralysis|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Congenital_myopathy_22A|_classic|Congenital_myopathy_22B|_severe_fetal|Congenital_myasthenic_syndrome_16|Inborn_genetic_diseases": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myasthenic_syndrome_16|Hyperkalemic_periodic_paralysis|Microcephaly|Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2": 1,
    "Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_1|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis|not_specified|not_provided": 1,
    "Congenital_myasthenic_syndrome_16|not_specified|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Paramyotonia_congenita_of_Von_Eulenburg|Potassium-aggravated_myotonia": 1,
    "Potassium-aggravated_myotonia|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis": 1,
    "Paramyotonia_congenita_of_Von_Eulenburg|Congenital_myopathy_22A|_classic|Hypokalemic_periodic_paralysis|_type_2|Congenital_myasthenic_syndrome_16|Congenital_myopathy_22B|_severe_fetal|Potassium-aggravated_myotonia|Hyperkalemic_periodic_paralysis": 1,
    "not_provided|Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Congenital_myasthenic_syndrome_16|Hypokalemic_periodic_paralysis|_type_2|Paramyotonia_congenita_of_Von_Eulenburg|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia": 1,
    "Congenital_myasthenic_syndrome_16|Paramyotonia_congenita_of_Von_Eulenburg|Hypokalemic_periodic_paralysis|_type_2|Hyperkalemic_periodic_paralysis|Potassium-aggravated_myotonia|not_provided": 1,
    "not_provided|PECAM1_POLYMORPHISM|Three_Vessel_Coronary_Disease": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 7,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 13,
    "Hereditary_spastic_paraplegia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_provided": 1,
    "POLG2-related_disorder|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 1,
    "Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|not_provided": 1,
    "not_provided|POLG2-related_spectrum_disorders": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 2,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)": 1,
    "not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|not_provided|Hereditary_spastic_paraplegia": 1,
    "Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 1,
    "Hereditary_spastic_paraplegia|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_provided|POLG2-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|not_provided": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_provided": 2,
    "Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)": 1,
    "Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_provided": 1,
    "not_provided|not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 1,
    "not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_specified": 1,
    "Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_specified|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)": 1,
    "POLG2-related_disorder": 2,
    "Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_provided": 1,
    "Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 1,
    "not_specified|not_provided|POLG2-related_disorder": 1,
    "POLG2-related_disorder|not_provided": 1,
    "not_specified|not_provided|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|Mitochondrial_DNA_depletion_syndrome_16A|Acute_liver_failure|not_provided": 1,
    "not_provided|POLG2-related_disorder": 4,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|not_specified|not_provided": 1,
    "not_specified|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_provided": 1,
    "not_provided|POLG2-related_disorder|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|Hereditary_spastic_paraplegia": 1,
    "Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|not_specified": 1,
    "not_provided|POLG2-related_disorder|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_16_(hepatic_type)|Progressive_external_ophthalmoplegia_with_mitochondrial_DNA_deletions|_autosomal_dominant_4|Mitochondrial_dna_depletion_syndrome_16B_(neuroophthalmic_type)|not_specified|not_provided": 1,
    "SMURF2-related_disorder": 11,
    "SMURF2-related_disorder|not_provided": 2,
    "not_provided|SMURF2-related_disorder": 1,
    "RGS9-related_disorder|not_provided": 6,
    "Bradyopsia|not_provided": 2,
    "not_provided|RGS9-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|RGS9-related_disorder|not_provided": 1,
    "not_provided|Bradyopsia": 1,
    "not_provided|RGS9-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Bradyopsia": 1,
    "Leber_congenital_amaurosis|not_provided|Bradyopsia": 1,
    "not_provided|Prolonged_electroretinal_response_suppression_1": 1,
    "Oligodontia-cancer_predisposition_syndrome": 1359,
    "not_provided|Oligodontia-cancer_predisposition_syndrome": 20,
    "Oligodontia-cancer_predisposition_syndrome|not_provided": 20,
    "Oligodontia-cancer_predisposition_syndrome|not_specified": 29,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 545,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 593,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome": 14,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_specified": 10,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided": 42,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome": 1,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 19,
    "Hereditary_cancer-predisposing_syndrome|not_specified|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 27,
    "not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|not_provided": 3,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 5,
    "Ovarian_cancer|not_provided|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 13,
    "not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 11,
    "Oligodontia-cancer_predisposition_syndrome|Ovarian_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 18,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 33,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome": 3,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|not_provided": 3,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 11,
    "not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 31,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome": 14,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 44,
    "Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|not_provided|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 5,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|AXIN2-related_disorder|Malignant_tumor_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|not_specified": 1,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome": 3,
    "Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome": 40,
    "Oligodontia|Colorectal_cancer|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome|not_provided|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|AXIN2-related_disorder": 1,
    "not_specified|Oligodontia-cancer_predisposition_syndrome": 9,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "AXIN2-related_disorder|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 3,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Carcinoma_of_colon|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 40,
    "Oligodontia-cancer_predisposition_syndrome|not_specified|Colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome": 2,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder": 1,
    "Oligodontia-cancer_predisposition_syndrome|Carcinoma_of_colon|not_specified|not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 12,
    "not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome": 3,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder": 1,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_specified|not_provided": 1,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 19,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome": 3,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder": 3,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 9,
    "not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 6,
    "AXIN2-related_attenuated_familial_adenomatous_polyposis|Oligodontia-cancer_predisposition_syndrome": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 10,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome|not_specified|AXIN2-related_disorder|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Tooth_agenesis|_selective|_1": 1,
    "Oligodontia-cancer_predisposition_syndrome|AXIN2-related_attenuated_familial_adenomatous_polyposis": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome": 3,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Aganglionic_megacolon": 1,
    "not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "AXIN2-related_attenuated_familial_adenomatous_polyposis": 4,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 6,
    "Oligodontia-cancer_predisposition_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 1,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer": 5,
    "not_provided|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Carcinoma_of_colon|Oligodontia-cancer_predisposition_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|AXIN2-related_attenuated_familial_adenomatous_polyposis": 1,
    "Ovarian_cancer|not_provided|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome": 8,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 2,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome": 1,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Oligodontia-cancer_predisposition_syndrome|Craniosynostosis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_specified": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 2,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 6,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome": 2,
    "Ovarian_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 1,
    "not_provided|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome": 1,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 4,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 8,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|not_specified": 3,
    "AXIN2-related_disorder|not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|not_provided|Oligodontia-cancer_predisposition_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|not_specified": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 10,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Colorectal_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided|Colorectal_cancer": 3,
    "not_provided|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 8,
    "Oligodontia-cancer_predisposition_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 2,
    "Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder": 1,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Oligodontia-cancer_predisposition_syndrome|not_provided": 1,
    "Colorectal_cancer|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|not_provided": 4,
    "not_provided|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 3,
    "AXIN2-related_disorder|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome": 1,
    "Colorectal_cancer|not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|not_specified": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|AXIN2-related_disorder|not_specified": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Oligodontia-cancer_predisposition_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_specified": 2,
    "Colorectal_cancer|not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Ovarian_cancer": 1,
    "not_provided|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 1,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|not_provided|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Oligodontia|Colorectal_cancer": 1,
    "not_specified|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|AXIN2-related_disorder|not_provided|Hereditary_cancer|Oligodontia-cancer_predisposition_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Oligodontia-cancer_predisposition_syndrome|not_specified|not_provided": 1,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|not_provided": 1,
    "AXIN2-related_disorder|not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|not_specified|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|not_specified|not_provided": 1,
    "not_provided|AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|AXIN2-related_disorder": 3,
    "Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|AXIN2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided|AXIN2-related_disorder": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified": 1,
    "AXIN2-related_disorder|Colorectal_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|not_provided|Colorectal_cancer": 1,
    "Colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_attenuated_familial_adenomatous_polyposis|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_specified|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|AXIN2-related_disorder": 1,
    "not_provided|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "AXIN2-related_disorder|Colorectal_cancer|Oligodontia|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome": 1,
    "Colorectal_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|AXIN2-related_disorder": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|Ovarian_cancer": 1,
    "Colorectal_carcinoma|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Tooth_agenesis|_selective|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|not_provided|Oligodontia-cancer_predisposition_syndrome": 1,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_specified|AXIN2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|not_provided|not_specified|AXIN2-related_disorder": 1,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Oligodontia-cancer_predisposition_syndrome": 1,
    "AXIN2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Ovarian_cancer|not_specified|Oligodontia-cancer_predisposition_syndrome": 1,
    "Oligodontia-cancer_predisposition_syndrome|Colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder": 1,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 1,
    "Colorectal_cancer|not_provided|Oligodontia-cancer_predisposition_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|AXIN2-related_disorder|not_specified": 1,
    "Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|AXIN2-related_disorder|not_provided": 1,
    "Colorectal_cancer|not_specified|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "AXIN2-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome": 1,
    "AXIN2-related_disorder|Oligodontia-cancer_predisposition_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Oligodontia-cancer_predisposition_syndrome|not_provided|not_specified": 1,
    "Ovarian_cancer|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "AXIN2-related_attenuated_familial_adenomatous_polyposis|Oligodontia-cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided": 1,
    "Spermatogenic_failure_44": 2,
    "Spermatogenic_failure_44|not_specified": 1,
    "CEP112-related_disorder": 1,
    "not_specified|Spermatogenic_failure_44": 1,
    "not_provided|APOH_POLYMORPHISM": 1,
    "PRKCA-related_disorder": 6,
    "not_provided|PRKCA-related_disorder": 1,
    "Pervasive_developmental_disorder": 1,
    "Stankiewicz-Isidor_syndrome": 21,
    "Stankiewicz-Isidor_syndrome|Inborn_genetic_diseases": 3,
    "PSMD12-related_disorder": 10,
    "Stankiewicz-Isidor_syndrome|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|PSMD12-related_disorder": 2,
    "Stankiewicz-Isidor_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Spermatogenic_failure_18|Stankiewicz-Isidor_syndrome": 1,
    "not_provided|Stankiewicz-Isidor_syndrome": 1,
    "BPTF-related_disorder|not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 1,
    "BPTF-related_disorder": 23,
    "BPTF-related_disorder|not_provided": 11,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_provided": 2,
    "Inborn_genetic_diseases|Kaposi_sarcoma|_susceptibility_to|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 1,
    "Inborn_genetic_diseases|BPTF-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 1,
    "BPTF-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|BPTF-related_disorder": 12,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 11,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|BPTF-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|BPTF-related_disorder|not_provided": 1,
    "BPTF-related_neurodevelopmental_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|Intellectual_disability|Secondary_microcephaly|Expressive_language_delay|Global_developmental_delay": 1,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 5,
    "not_provided|Inborn_genetic_diseases|Syndromic_intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|BPTF-related_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_provided": 4,
    "Inborn_genetic_diseases|Secondary_microcephaly|Expressive_language_delay|Global_developmental_delay": 1,
    "Secondary_microcephaly|Expressive_language_delay|Global_developmental_delay|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 2,
    "Secondary_microcephaly|Expressive_language_delay|Global_developmental_delay": 2,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_provided|Inborn_genetic_diseases": 1,
    "BPTF-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_specified|not_provided": 1,
    "Secondary_microcephaly|Expressive_language_delay|Global_developmental_delay|not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies": 1,
    "not_provided|BPTF-related_disorder|Inborn_genetic_diseases": 1,
    "Syndromic_intellectual_disability|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|BPTF-related_disorder": 1,
    "Inborn_genetic_diseases|Kaposi_sarcoma|Kaposi_sarcoma|_susceptibility_to|not_provided": 1,
    "Inborn_genetic_diseases|BPTF-related_disorder|Intellectual_disability|not_provided": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|not_specified": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|Secondary_microcephaly|Expressive_language_delay|Global_developmental_delay": 1,
    "AMZ2-related_disorder": 7,
    "AMZ2-related_disorder|not_provided": 1,
    "not_provided|ARSG-related_disorder": 12,
    "Usher_syndrome|_type_4|not_provided": 3,
    "Usher_syndrome|_type_4|Usher_syndrome": 1,
    "ARSG-related_disorder|not_provided": 7,
    "Usher_syndrome|_type_4": 9,
    "not_provided|Usher_syndrome|_type_4": 5,
    "Usher_syndrome|_type_4|ARSG-related_disorder|not_provided": 1,
    "not_provided|ARSG-related_disorder|not_specified": 1,
    "ARSG-related_disorder": 1,
    "WIPI1-related_disorder": 2,
    "Acrodysostosis_1_with_or_without_hormone_resistance|not_specified": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 40,
    "Carney_complex|_type_1": 476,
    "PRKAR1A-related_disorder": 3,
    "Carney_complex|Acrodysostosis": 7,
    "Acrodysostosis_1_with_or_without_hormone_resistance|PRKAR1A-related_disorder|Carney_complex|_type_1": 1,
    "PRKAR1A-related_disorder|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1": 1,
    "Carney_complex|_type_1|not_provided": 7,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 145,
    "not_provided|Carney_complex|_type_1": 14,
    "Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome": 90,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Carney_complex|_type_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|PRKAR1A-related_disorder|Carney_complex|_type_1": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Carney_complex|_type_1": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 5,
    "Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Acrodysostosis_1_with_or_without_hormone_resistance|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Carney_complex|_type_1|not_provided|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carney_complex|_type_1": 12,
    "Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Carney_complex|_type_1|PRKAR1A-related_disorder|not_provided|Acrodysostosis_1_with_or_without_hormone_resistance": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Carney_complex|_type_1": 7,
    "not_specified|PRKAR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Carney_complex|_type_1|PRKAR1A-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 4,
    "Familial_atrial_myxoma|Pigmented_nodular_adrenocortical_disease|_primary|_1|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance": 2,
    "Carney_complex|Acrodysostosis|Familial_atrial_myxoma|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|Acrodysostosis_1_with_or_without_hormone_resistance": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 2,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carney_complex|_type_1": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Hereditary_cancer-predisposing_syndrome|not_provided|Carney_complex|_type_1": 3,
    "Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|Acrodysostosis_1_with_or_without_hormone_resistance|Familial_atrial_myxoma": 1,
    "Carney_complex|_type_1|not_specified": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|PRKAR1A-related_disorder": 1,
    "Carney_complex|_type_1|Familial_atrial_myxoma|Acrodysostosis_1_with_or_without_hormone_resistance|Pigmented_nodular_adrenocortical_disease|_primary|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance": 6,
    "PRKAR1A-related_disorder|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "PRKAR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Carney_complex": 1,
    "PRKAR1A-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "PRKAR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Acrodysostosis_1_with_or_without_hormone_resistance": 2,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|not_specified": 2,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|not_provided": 2,
    "not_specified|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Hereditary_cancer-predisposing_syndrome|not_specified|Carney_complex|_type_1": 1,
    "not_specified|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|Medulloblastoma": 1,
    "Carney_complex|Acrodysostosis|Hereditary_cancer-predisposing_syndrome|not_specified|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|not_provided": 1,
    "PRKAR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Carney_complex|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Pigmented_nodular_adrenocortical_disease|_primary|_1|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Familial_atrial_myxoma|not_provided": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Familial_atrial_myxoma|Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Familial_atrial_myxoma|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "Carney_complex|_type_1|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance|Familial_atrial_myxoma|Pigmented_nodular_adrenocortical_disease|_primary|_1": 1,
    "not_provided|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome": 4,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Carney_complex|_type_1|not_provided": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PRKAR1A-related_disorder|not_provided|Carney_complex|_type_1|Familial_atrial_myxoma": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carney_complex|_type_1": 3,
    "Carney_complex|_type_1|not_provided|Carney_complex": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|PRKAR1A-related_disorder|not_provided|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "not_specified|Carney_complex|_type_1|Familial_atrial_myxoma": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Familial_atrial_myxoma|Pigmented_nodular_adrenocortical_disease|_primary|_1": 2,
    "not_specified|Carney_complex|_type_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Familial_atrial_myxoma|Pigmented_nodular_adrenocortical_disease|_primary|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carney_complex|_type_1|not_specified": 1,
    "Endocrine_pancreas_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|PRKAR1A-related_disorder|not_provided|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance": 1,
    "Familial_atrial_myxoma": 1,
    "not_provided|Carney_complex|Carney_complex|_type_1": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|not_provided": 1,
    "PRKAR1A-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1": 1,
    "Carney_complex|not_provided|Carney_complex|_type_1": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_1|Carney_complex|_type_1|Familial_atrial_myxoma|Acrodysostosis_1_with_or_without_hormone_resistance": 1,
    "Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance|PRKAR1A-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "PRKAR1A-related_disorder|not_specified|Carney_complex|_type_1": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|not_provided|Carney_complex|_type_1": 2,
    "Familial_atrial_myxoma|not_specified|Acrodysostosis_1_with_or_without_hormone_resistance|PRKAR1A-related_disorder|Carney_complex|_type_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Pigmented_nodular_adrenocortical_disease|_primary|_1|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Familial_atrial_myxoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Carney_complex|_type_1|not_provided|not_specified": 1,
    "PRKAR1A-related_disorder|Familial_atrial_myxoma|Pigmented_nodular_adrenocortical_disease|_primary|_1|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "PRKAR1A-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|not_provided": 1,
    "Adrenocortical_tumor|_somatic": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|not_provided": 1,
    "Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Albright_hereditary_osteodystrophy|_pseudohypoparathyroidism|_pseudopseudohypoparathyroidism|_acrodysostosis_and_osteoma_cutis|Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|not_provided": 1,
    "not_provided|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1|Pigmented_nodular_adrenocortical_disease|_primary|_1|Familial_atrial_myxoma|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carney_complex|_type_1|Familial_atrial_myxoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Carney_complex|_type_1": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_1|Carney_complex|Acrodysostosis_1_with_or_without_hormone_resistance|PRKAR1A-related_disorder|not_provided|Carney_complex|_type_1": 1,
    "Carney_complex|Acrodysostosis|not_provided": 8,
    "Carney_complex|_type_1|Acrodysostosis_1_with_or_without_hormone_resistance": 11,
    "not_provided|Acrodysostosis_1_with_or_without_hormone_resistance|Carney_complex|_type_1": 1,
    "Carney_complex|_type_1|not_provided|Acrodysostosis_1_with_or_without_hormone_resistance": 1,
    "Acrodysostosis|Carney_complex|not_provided": 1,
    "Amelogenesis_imperfecta_type_1G": 88,
    "Amelogenesis_imperfecta_type_1G|not_specified|not_provided": 1,
    "not_specified|not_provided|Acrodysostosis|Carney_complex": 1,
    "Amelogenesis_imperfecta_type_1G|Inborn_genetic_diseases": 3,
    "not_provided|Amelogenesis_imperfecta_type_1G": 14,
    "Amelogenesis_imperfecta_type_1G|FAM20A-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Amelogenesis_imperfecta_type_1G": 1,
    "Amelogenesis_imperfecta_type_1G|not_provided": 15,
    "Inborn_genetic_diseases|Amelogenesis_imperfecta_type_1G": 6,
    "Inborn_genetic_diseases|Amelogenesis_imperfecta_type_1G|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Amelogenesis_imperfecta_type_1G": 1,
    "FAM20A-related_disorder": 4,
    "not_provided|Amelogenesis_imperfecta_type_1G|Inborn_genetic_diseases": 1,
    "not_specified|Amelogenesis_imperfecta_type_1G|not_provided": 1,
    "not_provided|Amelogenesis_imperfecta_type_1G|FAM20A-related_disorder": 1,
    "Amelogenesis_imperfecta_type_1G|not_provided|FAM20A-related_disorder": 1,
    "FAM20A-related_disorder|Amelogenesis_imperfecta_type_1G": 1,
    "Amelogenesis_imperfecta_type_1G|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Amelogenesis_imperfecta_type_1G": 1,
    "Amelogenesis_imperfecta_type_1G|Inborn_genetic_diseases|not_provided": 1,
    "FAM20A-related_disorder|Amelogenesis_imperfecta_type_1G|not_provided": 1,
    "ABCA5-related_disorder": 15,
    "Inborn_genetic_diseases|Gingival_fibromatosis-hypertrichosis_syndrome": 1,
    "Gingival_fibromatosis-hypertrichosis_syndrome": 4,
    "ABCA5-related_disorder|not_provided": 3,
    "not_provided|ABCA5-related_disorder": 6,
    "See_cases|not_provided|ABCA5-related_disorder": 1,
    "Gingival_fibromatosis-hypertrichosis_syndrome|not_specified": 1,
    "Gingival_fibromatosis-hypertrichosis_syndrome|not_provided": 1,
    "Hypokalemic_tubulopathy_and_deafness": 12,
    "KCNJ16-related_disorder": 2,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9": 18,
    "not_provided|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 4,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9": 21,
    "Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 9,
    "Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided": 6,
    "Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|not_specified|Andersen_Tawil_syndrome": 1,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 43,
    "Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|not_provided|Andersen_Tawil_syndrome": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|not_provided": 1,
    "Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|not_provided": 3,
    "Familial_atrial_fibrillation|Short_QT_syndrome|Andersen_Tawil_syndrome": 9,
    "Short_QT_syndrome|Familial_atrial_fibrillation|Andersen_Tawil_syndrome": 2,
    "not_specified|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 1,
    "KCNJ2-related_disorder|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 150,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 4,
    "Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 22,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified|Atrial_fibrillation|_familial|_9": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype": 15,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_specified|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 3,
    "not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 9,
    "Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided": 4,
    "Andersen_Tawil_syndrome": 15,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Atrial_fibrillation|_familial|_9|not_provided|Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype": 4,
    "not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 8,
    "not_specified|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype": 1,
    "Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 4,
    "Familial_periodic_paralysis|Andersen_Tawil_syndrome": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided": 1,
    "Andersen_Tawil_syndrome|not_specified|not_provided|Short_QT_syndrome_type_3|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 4,
    "not_specified|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Congenital_long_QT_syndrome|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 6,
    "not_specified|Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 2,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Andersen_Tawil_syndrome": 3,
    "not_provided|Cardiovascular_phenotype|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Ventricular_tachycardia|Andersen_Tawil_syndrome|not_provided|Short_QT_syndrome_type_3|Supraventricular_tachycardia|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided|Cardiac_arrhythmia|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|not_provided|Long_QT_syndrome": 1,
    "not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype": 1,
    "not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9": 2,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 1,
    "Cardiovascular_phenotype|not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 5,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided": 2,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Congenital_long_QT_syndrome": 3,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_1|Atrial_fibrillation|_familial|_1|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|Congenital_long_QT_syndrome|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 2,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype|not_specified": 2,
    "Short_QT_syndrome_type_3|Short_QT_syndrome|Andersen_Tawil_syndrome": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Congenital_long_QT_syndrome": 3,
    "not_specified|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 2,
    "not_provided|Andersen_Tawil_syndrome": 3,
    "Andersen_Tawil_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiac_arrhythmia|not_specified|not_provided": 1,
    "Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_specified": 1,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided|Atrial_fibrillation|_familial|_9": 1,
    "KCNJ2-related_disorder|Andersen_Tawil_syndrome": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|not_provided": 1,
    "Andersen_Tawil_syndrome|Cardiovascular_phenotype|Short_QT_syndrome_type_3|not_specified|Atrial_fibrillation|_familial|_9": 1,
    "Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|not_provided": 2,
    "Short_QT_syndrome_type_3|not_provided": 1,
    "Congenital_long_QT_syndrome|not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Congenital_long_QT_syndrome|Andersen_Tawil_syndrome|not_provided|Cardiovascular_phenotype|Short_QT_syndrome_type_3": 1,
    "Short_QT_syndrome_type_3": 1,
    "not_provided|Short_QT_syndrome_type_3": 1,
    "Cardiac_arrhythmia|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 1,
    "Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiac_arrhythmia": 1,
    "Cardiovascular_phenotype|KCNJ2-related_disorder|Congenital_long_QT_syndrome|not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Cardiovascular_phenotype|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|not_provided": 1,
    "not_provided|Ventricular_fibrillation|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_specified|not_provided": 1,
    "KCNJ2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "not_specified|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome": 1,
    "Short_QT_syndrome|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided": 1,
    "not_specified|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype|not_specified|Atrial_fibrillation|_familial|_9|not_provided": 1,
    "not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided": 1,
    "not_specified|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype": 2,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|KCNJ2-related_disorder": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided": 2,
    "not_provided|not_specified|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Atrial_fibrillation|_familial|_9|not_provided|Cardiovascular_phenotype|not_specified|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|not_provided": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_specified|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_9": 1,
    "Andersen_Tawil_syndrome|Cardiovascular_phenotype|Familial_atrial_fibrillation|Short_QT_syndrome_type_3|Short_QT_syndrome": 1,
    "Long_QT_syndrome|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Cardiovascular_phenotype": 1,
    "Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Cardiovascular_phenotype|not_specified|Atrial_fibrillation|_familial|_9": 1,
    "KCNJ2-related_disorder|not_provided|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9": 1,
    "not_provided|Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9": 5,
    "Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3|not_provided": 1,
    "Familial_atrial_fibrillation|Short_QT_syndrome|not_provided|Andersen_Tawil_syndrome": 1,
    "Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3": 4,
    "Andersen_Tawil_syndrome|Familial_atrial_fibrillation|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3|Short_QT_syndrome": 1,
    "Short_QT_syndrome_type_3|not_provided|Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9": 1,
    "Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome": 8,
    "Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|not_provided|Andersen_Tawil_syndrome": 1,
    "Familial_atrial_fibrillation|Andersen_Tawil_syndrome|Short_QT_syndrome|not_provided": 1,
    "Familial_atrial_fibrillation|Andersen_Tawil_syndrome|Short_QT_syndrome": 1,
    "not_provided|Familial_atrial_fibrillation|Short_QT_syndrome|Andersen_Tawil_syndrome": 3,
    "not_provided|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome": 1,
    "Andersen_Tawil_syndrome|Familial_atrial_fibrillation|Short_QT_syndrome|Atrial_fibrillation|_familial|_9|Short_QT_syndrome_type_3": 1,
    "Familial_atrial_fibrillation|Short_QT_syndrome|Andersen_Tawil_syndrome|not_provided": 1,
    "Short_QT_syndrome_type_3|Andersen_Tawil_syndrome|Atrial_fibrillation|_familial|_9|not_provided": 1,
    "Andersen_Tawil_syndrome|not_provided|Short_QT_syndrome_type_3|Atrial_fibrillation|_familial|_9": 1,
    "not_provided|Atrial_fibrillation|_familial|_9|Andersen_Tawil_syndrome|Short_QT_syndrome_type_3": 1,
    "Short_QT_syndrome|Andersen_Tawil_syndrome|Familial_atrial_fibrillation": 1,
    "Camptomelic_dysplasia": 239,
    "Camptomelic_dysplasia|not_provided": 15,
    "Inborn_genetic_diseases|Camptomelic_dysplasia|not_provided": 1,
    "Camptomelic_dysplasia|not_specified": 3,
    "Camptomelic_dysplasia|Inborn_genetic_diseases": 9,
    "not_provided|SOX9-related_disorder|Camptomelic_dysplasia": 1,
    "SOX9-related_disorder": 15,
    "SOX9-related_disorder|Camptomelic_dysplasia|not_provided": 2,
    "CAMPOMELIC_DYSPLASIA_WITH_AUTOSOMAL_SEX_REVERSAL": 3,
    "ACAMPOMELIC_CAMPOMELIC_DYSPLASIA|Inborn_genetic_diseases": 1,
    "Camptomelic_dysplasia|not_provided|not_specified": 1,
    "not_provided|SOX9-related_disorder": 2,
    "SOX9-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Camptomelic_dysplasia": 16,
    "Bent_bone_dysplasia": 1,
    "Camptomelic_dysplasia|SOX9-related_disorder": 1,
    "Camptomelic_dysplasia|CAMPOMELIC_DYSPLASIA_WITH_AUTOSOMAL_SEX_REVERSAL": 3,
    "not_specified|Camptomelic_dysplasia|not_provided": 1,
    "ACAMPOMELIC_CAMPOMELIC_DYSPLASIA": 1,
    "Inborn_genetic_diseases|not_provided|Camptomelic_dysplasia": 2,
    "Connective_tissue_disorder|not_provided|not_specified|Camptomelic_dysplasia": 2,
    "not_provided|See_cases|Camptomelic_dysplasia|CAMPOMELIC_DYSPLASIA_WITH_AUTOSOMAL_SEX_REVERSAL": 1,
    "Camptomelic_dysplasia|ACAMPOMELIC_CAMPOMELIC_DYSPLASIA": 1,
    "Inborn_genetic_diseases|Camptomelic_dysplasia": 5,
    "SOX9-related_disorder|Camptomelic_dysplasia": 2,
    "Camptomelic_dysplasia|Intellectual_disability": 1,
    "not_specified|not_provided|Camptomelic_dysplasia": 3,
    "Camptomelic_dysplasia|CAMPOMELIC_DYSPLASIA_WITH_AUTOSOMAL_SEX_REVERSAL|not_provided": 1,
    "Camptomelic_dysplasia|not_provided|SOX9-related_disorder": 1,
    "Camptomelic_dysplasia|Connective_tissue_disorder": 1,
    "not_specified|Camptomelic_dysplasia": 1,
    "not_provided|Camptomelic_dysplasia|SOX9-related_disorder": 1,
    "SOX9-related_disorder|Camptomelic_dysplasia|Connective_tissue_disorder|not_provided": 1,
    "not_provided|Camptomelic_dysplasia|Inborn_genetic_diseases": 1,
    "Camptomelic_dysplasia|not_provided|Connective_tissue_disorder": 1,
    "not_provided|Camptomelic_dysplasia|not_specified|Connective_tissue_disorder": 1,
    "Camptomelic_dysplasia|not_provided|Connective_tissue_disorder|CAMPOMELIC_DYSPLASIA_WITH_AUTOSOMAL_SEX_REVERSAL": 1,
    "Congenital_disorder_of_glycosylation|COG1_congenital_disorder_of_glycosylation|not_provided": 1,
    "COG1_congenital_disorder_of_glycosylation": 265,
    "COG1_congenital_disorder_of_glycosylation|not_provided": 9,
    "not_provided|COG1_congenital_disorder_of_glycosylation": 10,
    "COG1_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 25,
    "Inborn_genetic_diseases|COG1_congenital_disorder_of_glycosylation": 28,
    "COG1-related_disorder|COG1_congenital_disorder_of_glycosylation": 2,
    "COG1_congenital_disorder_of_glycosylation|not_specified|not_provided": 4,
    "COG1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|COG1_congenital_disorder_of_glycosylation": 1,
    "not_provided|Inborn_genetic_diseases|COG1_congenital_disorder_of_glycosylation": 2,
    "COG1_congenital_disorder_of_glycosylation|COG1-related_disorder": 2,
    "COG1_congenital_disorder_of_glycosylation|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation": 1,
    "COG1-related_disorder|not_specified|not_provided|COG1_congenital_disorder_of_glycosylation": 1,
    "COG1-related_disorder|not_specified|not_provided|COG1_congenital_disorder_of_glycosylation|Intellectual_disability": 1,
    "COG1_congenital_disorder_of_glycosylation|Nephrotic_syndrome": 1,
    "not_provided|COG1_congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|COG1_congenital_disorder_of_glycosylation": 2,
    "COG1-related_disorder": 3,
    "COG1_congenital_disorder_of_glycosylation|not_provided|not_specified": 2,
    "not_specified|not_provided|COG1-related_disorder|COG1_congenital_disorder_of_glycosylation": 1,
    "not_provided|COG1_congenital_disorder_of_glycosylation|not_specified": 1,
    "COG1_congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "COG1_congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided": 1,
    "COG1_congenital_disorder_of_glycosylation|COG1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|COG1_congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|COG1_congenital_disorder_of_glycosylation|not_provided": 1,
    "SDK2-related_disorder": 41,
    "not_specified|SDK2-related_disorder": 3,
    "SDK2-related_disorder|not_specified": 1,
    "See_cases|SDK2-related_disorder|not_specified": 1,
    "not_provided|SDK2-related_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia_9": 2,
    "Primary_ciliary_dyskinesia_9": 28,
    "Primary_ciliary_dyskinesia_9|not_provided": 6,
    "DNAI2-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9": 32,
    "Primary_ciliary_dyskinesia_9|Primary_ciliary_dyskinesia|not_provided": 2,
    "Primary_ciliary_dyskinesia|DNAI2-related_disorder|Primary_ciliary_dyskinesia_9": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9|not_specified": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9|not_provided": 7,
    "not_provided|Primary_ciliary_dyskinesia|DNAI2-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9|DNAI2-related_disorder": 1,
    "Primary_ciliary_dyskinesia|not_provided|not_specified|Primary_ciliary_dyskinesia_9": 1,
    "Primary_ciliary_dyskinesia_9|Primary_ciliary_dyskinesia": 17,
    "DNAI2-related_disorder|Primary_ciliary_dyskinesia_9": 1,
    "Primary_ciliary_dyskinesia_9|not_provided|not_specified": 2,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9": 2,
    "not_provided|Primary_ciliary_dyskinesia_9|Primary_ciliary_dyskinesia|DNAI2-related_disorder": 1,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9": 5,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9|not_provided": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9": 1,
    "Primary_ciliary_dyskinesia_9|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia|DNAI2-related_disorder": 6,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9": 10,
    "Primary_ciliary_dyskinesia_9|Primary_ciliary_dyskinesia|not_specified": 1,
    "DNAI2-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_9|not_provided|Primary_ciliary_dyskinesia": 3,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_9": 2,
    "not_provided|Primary_ciliary_dyskinesia_9|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_9": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_9": 1,
    "not_provided|Primary_ciliary_dyskinesia|DNAI2-related_disorder|Primary_ciliary_dyskinesia_9": 1,
    "not_provided|Primary_ciliary_dyskinesia_9|not_specified": 1,
    "NHERF1-related_disorder": 4,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2|Inborn_genetic_diseases|NHERF1-related_disorder": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_2": 1,
    "NHERF1-related_disorder|not_provided": 1,
    "Dominant_hypophosphatemia_with_nephrolithiasis_or_osteoporosis": 2,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_2|not_provided": 2,
    "not_provided|NHERF1-related_disorder": 3,
    "not_specified|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2": 1,
    "Inborn_genetic_diseases|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2": 2,
    "NHERF1-related_disorder|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2|Chronic_kidney_disease": 1,
    "not_provided|NHERF1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|NHERF1-related_disorder|Hypophosphatemic_nephrolithiasis/osteoporosis_2": 1,
    "Dominant_hypophosphatemia_with_nephrolithiasis_or_osteoporosis|NHERF1-related_disorder|not_specified|not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2|Nephrolithiasis|Hypophosphatemia": 1,
    "not_provided|Inborn_genetic_diseases|Dominant_hypophosphatemia_with_nephrolithiasis_or_osteoporosis": 1,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2": 2,
    "not_provided|Dominant_hypophosphatemia_with_nephrolithiasis_or_osteoporosis": 1,
    "Hypophosphatemic_nephrolithiasis/osteoporosis_2|NHERF1-related_disorder|not_provided": 1,
    "not_provided|Hypophosphatemic_nephrolithiasis/osteoporosis_2|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hypophosphatemic_nephrolithiasis/osteoporosis_2": 1,
    "GRIN2C-related_disorder": 8,
    "Inborn_genetic_diseases|not_provided|Auditory_neuropathy-optic_atrophy_syndrome": 1,
    "Auditory_neuropathy-optic_atrophy_syndrome": 12,
    "not_provided|Auditory_neuropathy-optic_atrophy_syndrome": 2,
    "FDXR-related_disorder|not_provided": 8,
    "Auditory_neuropathy-optic_atrophy_syndrome|not_provided": 2,
    "Auditory_neuropathy-optic_atrophy_syndrome|Inborn_genetic_diseases": 2,
    "FDXR-related_disorder": 13,
    "Inborn_genetic_diseases|not_provided|FDXR-related_disorder": 1,
    "Inborn_genetic_diseases|FDXR-related_disorder|not_provided": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_9b|FDXR-related_disorder|Auditory_neuropathy-optic_atrophy_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|FDXR-related_disorder": 3,
    "Multiple_mitochondrial_dysfunctions_syndrome_9b|not_provided": 2,
    "Inborn_genetic_diseases|Auditory_neuropathy-optic_atrophy_syndrome|not_provided": 1,
    "Auditory_neuropathy-optic_atrophy_syndrome|Auditory_neuropathy": 1,
    "Auditory_neuropathy-optic_atrophy_syndrome|Multiple_mitochondrial_dysfunctions_syndrome_9b": 2,
    "Multiple_mitochondrial_dysfunctions_syndrome_9b|Optic_atrophy-ataxia-peripheral_neuropathy-global_developmental_delay_syndrome|Inborn_genetic_diseases|Auditory_neuropathy-optic_atrophy_syndrome": 1,
    "Inborn_genetic_diseases|FDXR-related_disorder": 1,
    "Auditory_neuropathy-optic_atrophy_syndrome|Inborn_genetic_diseases|not_provided|FDXR-related_disorder": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_9b": 1,
    "Multiple_mitochondrial_dysfunctions_syndrome_9b|Auditory_neuropathy-optic_atrophy_syndrome|not_provided": 1,
    "Usher_syndrome_type_1G|not_provided": 19,
    "not_provided|Usher_syndrome_type_1G": 7,
    "not_provided|USH1G-related_disorder": 2,
    "Rare_genetic_deafness|not_provided|Usher_syndrome_type_1G": 1,
    "USH1G-related_disorder|not_provided": 3,
    "Usher_syndrome_type_1G|Retinal_dystrophy|not_provided|USH1G-related_disorder|not_specified": 1,
    "not_provided|Usher_syndrome_type_1G|not_specified": 1,
    "not_specified|not_provided|Non-Syndromic_Hereditary_Hearing_Impairment": 1,
    "USH1G-related_disorder|not_specified|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_18A|not_provided|Retinal_dystrophy|Inborn_genetic_diseases": 1,
    "Usher_syndrome_type_1G|Usher_syndrome_type_1": 1,
    "not_provided|Retinal_dystrophy|not_specified|USH1G-related_disorder|Usher_syndrome_type_1G|Optic_atrophy": 1,
    "not_specified|not_provided|Usher_syndrome|Usher_syndrome_type_1G": 1,
    "not_specified|not_provided|USH1G-related_disorder": 2,
    "Inborn_genetic_diseases|Usher_syndrome_type_1G|not_provided": 1,
    "Usher_syndrome_type_1G|not_specified|USH1G-related_disorder|not_provided": 1,
    "Usher_syndrome_type_1G|Inborn_genetic_diseases|not_provided": 1,
    "Usher_syndrome_type_1G|Deafness|Hearing_loss|_autosomal_recessive": 1,
    "not_specified|Usher_syndrome_type_1G|not_provided": 1,
    "USH1G-related_disorder": 1,
    "not_provided|not_specified|Usher_syndrome_type_1G": 1,
    "Usher_syndrome_type_1|Usher_syndrome_type_1G": 1,
    "Usher_syndrome_type_1G|not_provided|not_specified": 1,
    "not_specified|Hearing_impairment|Usher_syndrome_type_1G|not_provided": 1,
    "not_specified|not_provided|Usher_syndrome_type_1G|Optic_atrophy": 1,
    "Retinal_dystrophy|not_provided|not_specified|USH1G-related_disorder": 1,
    "Usher_syndrome_type_1G|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy_105_with_hypopituitarism": 8,
    "NUP85-related_disorder|not_provided": 3,
    "not_provided|NUP85-related_disorder": 5,
    "not_provided|Nephrotic_syndrome|_type_17": 2,
    "Nephrotic_syndrome|_type_17": 7,
    "not_provided|NUP85-related_disorder|Nephrotic_syndrome|_type_17": 2,
    "NUP85-related_disorder": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_deficiency_34": 1,
    "MRPS7-related_disorder|not_specified|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency_34|not_provided": 2,
    "not_provided|MRPS7-related_disorder": 4,
    "Premature_ovarian_insufficiency|Sensorineural_hearing_loss_disorder": 1,
    "MRPS7-related_disorder": 2,
    "Combined_oxidative_phosphorylation_deficiency_34": 1,
    "not_specified|Sensorineural_hearing_loss_disorder|Premature_ovarian_insufficiency|not_provided": 1,
    "See_cases|not_provided|Combined_oxidative_phosphorylation_deficiency_34": 1,
    "not_provided|Amish_lethal_microcephaly": 5,
    "Amish_lethal_microcephaly": 12,
    "Amish_lethal_microcephaly|not_provided": 6,
    "SLC25A19-related_disorder": 1,
    "not_specified|Amish_lethal_microcephaly|not_provided|Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis": 2,
    "Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis": 10,
    "SLC25A19-related_disorder|Amish_lethal_microcephaly|not_provided": 1,
    "SLC25A19-related_disorder|Inborn_genetic_diseases|not_specified|Amish_lethal_microcephaly|not_provided": 1,
    "not_provided|not_specified|SLC25A19-related_disorder": 1,
    "not_provided|not_specified|Amish_lethal_microcephaly": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis": 1,
    "Inborn_genetic_diseases|not_provided|Amish_lethal_microcephaly": 2,
    "Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis|not_provided|Amish_lethal_microcephaly": 2,
    "not_provided|SLC25A19-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis": 1,
    "not_specified|not_provided|Amish_lethal_microcephaly": 2,
    "not_specified|Amish_lethal_microcephaly|not_provided": 1,
    "Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis|not_provided": 1,
    "Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis|Amish_lethal_microcephaly": 1,
    "Amish_lethal_microcephaly|not_specified|not_provided|Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis": 1,
    "Inborn_genetic_diseases|Amish_lethal_microcephaly|not_provided": 1,
    "not_provided|not_specified|Amish_lethal_microcephaly|SLC25A19-related_disorder": 1,
    "Amish_lethal_microcephaly|Progressive_demyelinating_neuropathy_with_bilateral_striatal_necrosis|not_specified|not_provided": 1,
    "TMEM94-related_disorder": 22,
    "Inborn_genetic_diseases|TMEM94-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_developmental_disorder_with_cardiac_defects_and_dysmorphic_facies": 1,
    "TMEM94-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder_with_cardiac_defects_and_dysmorphic_facies": 28,
    "TMEM94-related_disorder|Intellectual_developmental_disorder_with_cardiac_defects_and_dysmorphic_facies": 2,
    "TMEM94-related_disorder|not_provided": 3,
    "Rare_syndromic_intellectual_disability|Intellectual_developmental_disorder_with_cardiac_defects_and_dysmorphic_facies": 1,
    "not_provided|TMEM94-related_disorder": 2,
    "Intellectual_developmental_disorder_with_cardiac_defects_and_dysmorphic_facies|not_provided": 3,
    "Inborn_genetic_diseases|Rare_syndromic_intellectual_disability": 1,
    "TMEM94-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_cardiac_defects_and_dysmorphic_facies": 1,
    "Inborn_genetic_diseases|not_provided|TMEM94-related_disorder": 1,
    "Olivopontocerebellar_hypoplasia": 4,
    "not_provided|Pontocerebellar_hypoplasia_type_4|not_specified|Pontoneocerebellar_hypoplasia": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_5|not_specified|not_provided|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_4": 2,
    "not_provided|TSEN54-related_disorder": 3,
    "TSEN54-related_disorder": 5,
    "Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|not_specified|Inborn_genetic_diseases|Pontoneocerebellar_hypoplasia|TSEN54-related_disorder": 1,
    "Pontoneocerebellar_hypoplasia|not_specified|not_provided|Pontocerebellar_hypoplasia_type_4": 1,
    "Pontocerebellar_hypoplasia_type_2A": 8,
    "Pontocerebellar_hypoplasia_type_2A|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_4": 5,
    "not_provided|Pontocerebellar_hypoplasia_type_4": 2,
    "not_provided|not_specified|Pontoneocerebellar_hypoplasia": 2,
    "not_provided|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4|not_specified": 1,
    "Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|not_specified": 1,
    "Pontocerebellar_hypoplasia_type_2A|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_4|not_specified|Pontocerebellar_hypoplasia_type_5|Pontoneocerebellar_hypoplasia": 1,
    "TSEN54-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_5": 1,
    "Pontocerebellar_hypoplasia_type_5": 3,
    "Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|not_provided": 2,
    "not_provided|not_specified|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A": 1,
    "Pontocerebellar_hypoplasia_type_2A|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|not_provided": 5,
    "TSEN54-related_disorder|not_provided|Pontoneocerebellar_hypoplasia": 2,
    "Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4|not_provided": 1,
    "Inborn_genetic_diseases|Pontoneocerebellar_hypoplasia|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4": 1,
    "not_provided|Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_4|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4|not_provided|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_5|Pontocerebellar_hypoplasia_type_4|Methylmalonic_aciduria_and_homocystinuria_type_cblD|TSEN54-related_disorder|Pontocerebellar_hypoplasia_type_2|TSEN54_Pontocerebellar_Hypoplasia|Inborn_genetic_diseases|Pontoneocerebellar_hypoplasia|Pontocerebellar_hypoplasia_type_2A|not_provided|Congenital_cerebellar_hypoplasia|Intellectual_disability|Microcephaly|Global_developmental_delay|Hypertonia|Amblyopia|Olivopontocerebellar_hypoplasia": 1,
    "not_provided|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A": 1,
    "Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|Inborn_genetic_diseases|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_5|Methylmalonic_aciduria_and_homocystinuria_type_cblD|not_provided": 1,
    "not_specified|not_provided|TSEN54-related_disorder": 1,
    "not_provided|Olivopontocerebellar_hypoplasia": 1,
    "Pontocerebellar_hypoplasia_type_2A|not_provided|Inborn_genetic_diseases": 1,
    "Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|TSEN54-related_disorder|not_provided": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_5|Inborn_genetic_diseases": 1,
    "Olivopontocerebellar_hypoplasia|Inborn_genetic_diseases|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_5|not_specified|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontoneocerebellar_hypoplasia|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_4|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|TSEN54-related_disorder|Pontoneocerebellar_hypoplasia": 1,
    "Olivopontocerebellar_hypoplasia|not_provided": 1,
    "not_specified|not_provided|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_5|Pontoneocerebellar_hypoplasia": 1,
    "Pontocerebellar_hypoplasia_type_4|Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_5|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Olivopontocerebellar_hypoplasia|Pontoneocerebellar_hypoplasia": 1,
    "TSEN54-related_disorder|Pontoneocerebellar_hypoplasia|not_specified|not_provided": 1,
    "Pontocerebellar_hypoplasia_type_5|Pontoneocerebellar_hypoplasia": 1,
    "Pontoneocerebellar_hypoplasia|not_specified|TSEN54-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_2A|Pontocerebellar_hypoplasia_type_4|not_provided|Pontocerebellar_hypoplasia_type_5|Pontoneocerebellar_hypoplasia|not_specified": 1,
    "RECQL5-related_disorder": 73,
    "not_specified|RECQL5-related_disorder": 6,
    "not_provided|RECQL5-related_disorder": 9,
    "RECQL5-related_disorder|not_specified": 2,
    "RECQL5-related_disorder|not_provided": 2,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases|not_provided": 6,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided": 4,
    "not_provided|ITGB4-related_disorder": 36,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate": 187,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases": 26,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate": 16,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 6,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|See_cases": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases|ITGB4-related_disorder": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided|Inborn_genetic_diseases": 8,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 13,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate": 17,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|ITGB4-related_disorder|not_provided": 5,
    "not_provided|ITGB4-related_disorder|Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided": 59,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|Epidermolysis_bullosa|_junctional_5A|_intermediate|ITGB4-related_disorder": 1,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|ITGB4-related_disorder": 1,
    "Inborn_genetic_diseases|ITGB4-related_disorder": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases": 4,
    "ITGB4-related_disorder|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 9,
    "ITGB4-related_disorder|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 7,
    "not_provided|Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Abnormality_of_the_skin": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases": 5,
    "not_provided|Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 6,
    "ITGB4-related_disorder": 21,
    "Inborn_genetic_diseases|ITGB4-related_disorder|not_provided": 1,
    "not_provided|ITGB4-related_disorder|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 2,
    "ITGB4-related_disorder|not_provided": 5,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate": 4,
    "Multiple_sclerosis|Inborn_genetic_diseases|not_provided|ITGB4-related_disorder|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases|not_provided": 3,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided|Myoepithelial_tumor": 1,
    "ITGB4-related_disorder|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa_simplex_1C|_localized": 1,
    "ITGB4-related_disorder|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|not_specified": 1,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|ITGB4-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_specified|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Nephrotic_syndrome": 1,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|ITGB4-related_disorder|not_provided": 3,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|ITGB4-related_disorder": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate": 2,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Epidermolysis_bullosa_simplex_1C|_localized|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Junctional_epidermolysis_bullosa|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa|not_provided": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 2,
    "not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|ITGB4-related_disorder": 1,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|not_specified|Deficiency_of_galactokinase|Epidermolysis_bullosa_simplex_1C|_localized|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Epidermolysis_bullosa|_junctional_5A|_intermediate|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa|_junctional_5A|_intermediate|not_provided|ITGB4-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 2,
    "not_provided|Epidermolysis_bullosa_simplex_1C|_localized|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Deficiency_of_galactokinase|not_provided|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "ITGB4-related_disorder|Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "not_provided|Deficiency_of_galactokinase": 10,
    "not_provided|Deficiency_of_galactokinase|Epidermolysis_bullosa|_junctional_5A|_intermediate|Epidermolysis_bullosa_simplex_1C|_localized|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Epidermolysis_bullosa|_junctional_5A|_intermediate|Junctional_epidermolysis_bullosa_with_pyloric_atresia|ITGB4-related_disorder": 1,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_1C|_localized|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "not_specified|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Deficiency_of_galactokinase|not_provided|Epidermolysis_bullosa_simplex_1C|_localized|Junctional_epidermolysis_bullosa_with_pyloric_atresia": 1,
    "Deficiency_of_galactokinase|Junctional_epidermolysis_bullosa_with_pyloric_atresia|not_provided": 1,
    "Deficiency_of_galactokinase|Junctional_epidermolysis_bullosa_with_pyloric_atresia|Epidermolysis_bullosa_simplex_1C|_localized|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Deficiency_of_galactokinase|not_specified": 5,
    "Deficiency_of_galactokinase|Inborn_genetic_diseases": 4,
    "Junctional_epidermolysis_bullosa_with_pyloric_atresia|Deficiency_of_galactokinase|not_provided": 1,
    "Inborn_genetic_diseases|Deficiency_of_galactokinase": 8,
    "GALK1-related_disorder|Deficiency_of_galactokinase": 5,
    "Deficiency_of_galactokinase|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|GALK1-related_disorder|Deficiency_of_galactokinase": 1,
    "Deficiency_of_galactokinase|not_provided": 6,
    "not_specified|Deficiency_of_galactokinase": 3,
    "Deficiency_of_galactokinase|GALK1-related_disorder": 1,
    "GALK1-related_disorder|Inborn_genetic_diseases": 1,
    "GALK1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Deficiency_of_galactokinase": 1,
    "not_specified|GALK1-related_disorder|Deficiency_of_galactokinase": 1,
    "GALK1-related_disorder": 1,
    "not_specified|not_provided|Deficiency_of_galactokinase": 1,
    "Deficiency_of_galactokinase|GALK1-related_disorder|not_provided": 1,
    "H3-3B-related_disorder|Bryant-Li-Bhoj_neurodevelopmental_syndrome_2": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_2": 11,
    "Hemiparkinsonism-hemiatrophy_syndrome": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_2|Intellectual_disability|Global_developmental_delay|Brain_imaging_abnormality|Delayed_speech_and_language_development|Short_stature": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Brain_imaging_abnormality|Delayed_speech_and_language_development|Intellectual_disability|Global_developmental_delay|Short_stature": 1,
    "Bryant-Li-Bhoj_neurodevelopmental_syndrome_2|Brain_imaging_abnormality|Delayed_speech_and_language_development|Short_stature|Global_developmental_delay|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_provided|Bryant-Li-Bhoj_neurodevelopmental_syndrome_2|Delayed_speech_and_language_development|Brain_imaging_abnormality|Global_developmental_delay|Intellectual_disability|Short_stature|Inborn_genetic_diseases": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3": 1282,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_provided": 26,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3": 17,
    "Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder": 6,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Inborn_genetic_diseases": 35,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_3": 27,
    "not_specified|Autoinflammatory_syndrome|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 3,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_specified": 16,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 17,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_3": 5,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Inborn_genetic_diseases|not_specified": 3,
    "not_specified|not_provided|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3": 3,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Inborn_genetic_diseases|not_provided": 2,
    "UNC13D-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_3|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 10,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_3": 10,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified": 6,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified": 3,
    "Familial_hemophagocytic_lymphohistiocytosis|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome": 7,
    "UNC13D-related_disorder|not_specified|Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_provided": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Familial_hemophagocytic_lymphohistiocytosis": 5,
    "not_specified|UNC13D-related_disorder": 1,
    "UNC13D-related_disorder": 9,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Intellectual_disability": 1,
    "UNC13D-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_3": 7,
    "Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 2,
    "UNC13D-related_disorder|Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_3|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_provided": 3,
    "not_specified|See_cases|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified|not_provided": 1,
    "UNC13D-related_disorder|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 3,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3|not_provided": 2,
    "Familial_hemophagocytic_lymphohistiocytosis|not_specified|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "UNC13D-related_disorder|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Familial_hemophagocytic_lymphohistiocytosis|Autoinflammatory_syndrome|not_provided": 1,
    "UNC13D-related_disorder|Autoinflammatory_syndrome|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3|Intellectual_disability": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_provided|not_specified": 2,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_3|Inborn_genetic_diseases": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|See_cases": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_specified": 2,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3|Inborn_genetic_diseases": 2,
    "not_provided|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_specified|not_provided": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder|Inborn_genetic_diseases": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_provided|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_provided|not_specified": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_specified|Autoinflammatory_syndrome": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_specified|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|not_provided|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Familial_hemophagocytic_lymphohistiocytosis|not_provided": 2,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_3": 2,
    "not_provided|UNC13D-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|UNC13D-related_disorder|Autoinflammatory_syndrome|not_specified": 1,
    "UNC13D-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_3|not_provided": 1,
    "Autoinflammatory_syndrome|UNC13D-related_disorder|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified": 1,
    "Autoinflammatory_syndrome|not_provided|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|See_cases|Inborn_genetic_diseases": 1,
    "See_cases|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "not_provided|Inborn_genetic_diseases|UNC13D-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|UNC13D-related_disorder": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_3|Autoinflammatory_syndrome|not_specified": 1,
    "Autoinflammatory_syndrome|UNC13D-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_3|not_specified": 1,
    "not_provided|UNC13D-related_disorder|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3": 1,
    "UNC13D-related_disorder|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_3|not_provided": 1,
    "Hearing_loss|_autosomal_recessive_107": 4,
    "WBP2-related_disorder": 1,
    "WBP2-related_disorder|not_provided": 3,
    "not_provided|WBP2-related_disorder": 2,
    "Hearing_loss|_autosomal_recessive_107|not_specified|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_recessive_107": 3,
    "Acyl-CoA_oxidase_deficiency|not_provided": 23,
    "Acyl-CoA_oxidase_deficiency": 692,
    "not_provided|Acyl-CoA_oxidase_deficiency": 14,
    "Acyl-CoA_oxidase_deficiency|Mitchell_syndrome|not_provided": 2,
    "Acyl-CoA_oxidase_deficiency|Mitchell_syndrome": 11,
    "Acyl-CoA_oxidase_deficiency|Inborn_genetic_diseases": 17,
    "not_provided|Acyl-CoA_oxidase_deficiency|not_specified|ACOX1-related_disorder": 1,
    "Mitchell_syndrome|Acyl-CoA_oxidase_deficiency": 9,
    "Mitchell_syndrome|not_provided|Acyl-CoA_oxidase_deficiency": 4,
    "Acyl-CoA_oxidase_deficiency|not_specified": 3,
    "ACOX1-related_disorder|Acyl-CoA_oxidase_deficiency": 5,
    "not_provided|ACOX1-related_disorder|Inborn_genetic_diseases|Acyl-CoA_oxidase_deficiency": 1,
    "Inborn_genetic_diseases|Acyl-CoA_oxidase_deficiency": 6,
    "Mitchell_syndrome": 9,
    "ACOX1-related_disorder|Inborn_genetic_diseases|Acyl-CoA_oxidase_deficiency": 1,
    "Inborn_genetic_diseases|Mitchell_syndrome": 1,
    "not_specified|Acyl-CoA_oxidase_deficiency": 3,
    "ACOX1-related_disorder|Acyl-CoA_oxidase_deficiency|not_provided": 1,
    "Acyl-CoA_oxidase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "ACOX1-related_disorder|not_provided|Acyl-CoA_oxidase_deficiency": 3,
    "Acyl-CoA_oxidase_deficiency|not_provided|not_specified": 1,
    "Acyl-CoA_oxidase_deficiency|ACOX1-related_disorder": 2,
    "not_specified|Acyl-CoA_oxidase_deficiency|Mitchell_syndrome|not_provided": 1,
    "not_specified|not_provided|Acyl-CoA_oxidase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Acyl-CoA_oxidase_deficiency|Mitchell_syndrome": 1,
    "Inborn_genetic_diseases|ACOX1-related_disorder|Acyl-CoA_oxidase_deficiency|not_provided|Mitchell_syndrome": 1,
    "ACOX1-related_disorder|Acyl-CoA_oxidase_deficiency|Inborn_genetic_diseases": 1,
    "Acyl-CoA_oxidase_deficiency|Mitchell_syndrome|not_specified|not_provided": 1,
    "not_provided|Acyl-CoA_oxidase_deficiency|Mitchell_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Acyl-CoA_oxidase_deficiency": 1,
    "ACOX1-related_disorder": 2,
    "Acyl-CoA_oxidase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Neutropenia|_severe_congenital|_10|_autosomal_recessive": 1,
    "Neurodevelopmental_disorder_with_seizures_and_brain_atrophy": 10,
    "Neurodevelopmental_disorder_with_seizures_and_brain_atrophy|Inborn_genetic_diseases": 1,
    "EXOC7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_seizures_and_brain_atrophy": 1,
    "not_provided|Neurodevelopmental_disorder_with_seizures_and_brain_atrophy": 1,
    "not_provided|EXOC7-related_disorder|See_cases": 1,
    "FOXJ1-related_disorder": 16,
    "Ciliary_dyskinesia|_primary|_43": 13,
    "Ciliary_dyskinesia|_primary|_43|Inborn_genetic_diseases": 1,
    "Ciliary_dyskinesia|_primary|_43|not_provided": 1,
    "Inborn_genetic_diseases|FOXJ1-related_disorder": 1,
    "FOXJ1-related_disorder|Inborn_genetic_diseases": 1,
    "Chronic_granulomatous_disease|Williams_syndrome": 1,
    "QRICH2-related_disorder": 45,
    "Spermatogenic_failure_35": 7,
    "not_provided|Spermatogenic_failure_35|QRICH2-related_disorder": 1,
    "not_provided|QRICH2-related_disorder": 6,
    "not_provided|Spermatogenic_failure_35": 3,
    "QRICH2-related_disorder|not_provided": 1,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 150,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|not_provided": 30,
    "RHBDF2-related_disorder": 2,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|Inborn_genetic_diseases": 15,
    "not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 23,
    "not_provided|Inborn_genetic_diseases|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 4,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|not_provided|Inborn_genetic_diseases": 6,
    "not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|RHBDF2-related_disorder": 1,
    "not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 4,
    "not_provided|RHBDF2-related_disorder": 3,
    "RHBDF2-related_disorder|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|not_provided": 1,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|RHBDF2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 8,
    "not_specified|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|not_provided": 1,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|RHBDF2-related_disorder|not_provided": 2,
    "RHBDF2-related_disorder|not_provided": 1,
    "Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "RHBDF2-related_disorder|not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 3,
    "RHBDF2-related_disorder|Inborn_genetic_diseases|not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 1,
    "not_specified|not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 3,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome|not_provided": 1,
    "RHBDF2-related_disorder|not_specified|not_provided|Palmoplantar_keratoderma-esophageal_carcinoma_syndrome": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_36|Retinal_dystrophy|not_provided": 2,
    "Retinitis_pigmentosa_36|not_provided": 1,
    "Retinitis_pigmentosa_36": 2,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_36|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Retinitis_pigmentosa_36|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_36": 1,
    "not_provided|Inborn_genetic_diseases|Retinitis_pigmentosa_36": 1,
    "ST6GALNAC1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_44": 1,
    "Intellectual_disability|_autosomal_recessive_44": 14,
    "METTL23-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_44|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_recessive_44|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_44": 2,
    "Intellectual_disability|_autosomal_recessive_44|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_recessive_44": 1,
    "METTL23-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_44": 1,
    "Acute_myeloid_leukemia|Atypical_chronic_myeloid_leukemia|_BCR-ABL1_negative": 1,
    "SRSF2-related_disorder": 1,
    "not_provided|SEPTIN9-related_disorder": 5,
    "Hereditary_Neuralgic_Amyotrophy_(HNA)": 9,
    "Amyotrophic_neuralgia": 55,
    "Amyotrophic_neuralgia|not_provided": 22,
    "not_provided|Amyotrophic_neuralgia": 31,
    "not_provided|Hereditary_Neuralgic_Amyotrophy_(HNA)": 1,
    "not_provided|not_specified|Amyotrophic_neuralgia": 4,
    "SEPTIN9-related_disorder|not_provided": 2,
    "not_specified|not_provided|Amyotrophic_neuralgia": 3,
    "Inborn_genetic_diseases|not_provided|Amyotrophic_neuralgia": 2,
    "Inborn_genetic_diseases|SEPTIN9-related_disorder": 1,
    "not_specified|Amyotrophic_neuralgia|not_provided": 1,
    "Inborn_genetic_diseases|SEPTIN9-related_disorder|not_provided|Amyotrophic_neuralgia": 1,
    "not_provided|Amyotrophic_neuralgia|not_specified": 1,
    "not_provided|Amyotrophic_neuralgia|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|_type_I": 1,
    "not_provided|SEPTIN9-related_disorder|Amyotrophic_neuralgia|Inborn_genetic_diseases|not_specified": 1,
    "Amyotrophic_neuralgia|not_provided|not_specified": 2,
    "SEPTIN9-related_disorder": 5,
    "Neuralgic_amyotrophy|not_provided": 1,
    "Amyotrophic_neuralgia|SEPTIN9-related_disorder": 1,
    "not_provided|Amyotrophic_neuralgia|Inborn_genetic_diseases": 3,
    "SEPTIN9-related_disorder|not_specified|Amyotrophic_neuralgia|not_provided": 1,
    "SEPTIN9-related_disorder|not_provided|Amyotrophic_neuralgia": 1,
    "Cleft_palate|not_provided": 2,
    "Charcot-Marie-Tooth_disease|_type_I|not_specified|not_provided|Amyotrophic_neuralgia": 1,
    "Inborn_genetic_diseases|Amyotrophic_neuralgia|not_specified|not_provided": 1,
    "not_provided|Amyotrophic_neuralgia|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Amyotrophic_neuralgia|Hereditary_Neuralgic_Amyotrophy_(HNA)": 1,
    "Hereditary_Neuralgic_Amyotrophy_(HNA)|not_provided": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_1": 10,
    "Epidermodysplasia_verruciformis": 1036,
    "Epidermodysplasia_verruciformis|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 3,
    "Inborn_genetic_diseases|Epidermodysplasia_verruciformis": 49,
    "TMC6-related_disorder|Epidermodysplasia_verruciformis|not_provided": 4,
    "TMC6-related_disorder|Epidermodysplasia_verruciformis": 5,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_1|Epidermodysplasia_verruciformis": 4,
    "Epidermodysplasia_verruciformis|Inborn_genetic_diseases": 80,
    "Epidermodysplasia_verruciformis|Inborn_genetic_diseases|not_provided": 2,
    "Epidermodysplasia_verruciformis|not_specified|not_provided": 5,
    "not_provided|Epidermodysplasia_verruciformis": 19,
    "Epidermodysplasia_verruciformis|not_provided": 26,
    "Epidermodysplasia_verruciformis|not_provided|TMC6-related_disorder": 1,
    "not_specified|Epidermodysplasia_verruciformis|not_provided": 2,
    "TMC6-related_disorder|Epidermodysplasia_verruciformis|not_provided|not_specified": 1,
    "Epidermodysplasia_verruciformis|Inborn_genetic_diseases|TMC6-related_disorder": 1,
    "Epidermodysplasia_verruciformis|Inborn_genetic_diseases|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 2,
    "not_provided|Epidermodysplasia_verruciformis|not_specified": 1,
    "Epidermodysplasia_verruciformis|not_provided|Inborn_genetic_diseases": 3,
    "Epidermodysplasia_verruciformis|TMC6-related_disorder": 4,
    "not_provided|Epidermodysplasia_verruciformis|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 1,
    "Epidermodysplasia_verruciformis|TMC6-related_disorder|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 1,
    "Epidermodysplasia_verruciformis|not_provided|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|Epidermodysplasia_verruciformis": 1,
    "Inborn_genetic_diseases|Epidermodysplasia_verruciformis|TMC6-related_disorder": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_1|Epidermodysplasia_verruciformis|not_provided": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_1|Epidermodysplasia_verruciformis|Inborn_genetic_diseases": 1,
    "Epidermodysplasia_verruciformis|Epidermodysplasia_verruciformis|_susceptibility_to|_2|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 1,
    "Epidermodysplasia_verruciformis|not_specified|TMC8-related_disorder|not_provided": 1,
    "TMC8-related_disorder|Epidermodysplasia_verruciformis": 5,
    "Epidermodysplasia_verruciformis|not_specified": 1,
    "Epidermodysplasia_verruciformis|TMC8-related_disorder": 4,
    "not_provided|not_specified|Epidermodysplasia_verruciformis": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_2": 2,
    "Epidermodysplasia_verruciformis|Epidermodysplasia_verruciformis|_susceptibility_to|_2": 1,
    "Epidermodysplasia_verruciformis|Epidermodysplasia_verruciformis|_susceptibility_to|_2|not_specified|not_provided": 2,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_2|Epidermodysplasia_verruciformis|not_provided": 1,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_2|Epidermodysplasia_verruciformis": 4,
    "Epidermodysplasia_verruciformis|not_specified|Epidermodysplasia_verruciformis|_susceptibility_to|_2|not_provided": 1,
    "TMC8-related_disorder|Epidermodysplasia_verruciformis|_susceptibility_to|_2|Epidermodysplasia_verruciformis": 1,
    "TMC8-related_disorder|Epidermodysplasia_verruciformis|_susceptibility_to|_2|Epidermodysplasia_verruciformis|not_provided|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 1,
    "TMC8-related_disorder|Epidermodysplasia_verruciformis|not_provided": 2,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_1|Epidermodysplasia_verruciformis|_susceptibility_to|_2": 3,
    "Epidermodysplasia_verruciformis|_susceptibility_to|_1|Epidermodysplasia_verruciformis|_susceptibility_to|_2|Epidermodysplasia_verruciformis|not_provided": 1,
    "Epidermodysplasia_verruciformis|Inborn_genetic_diseases|TMC8-related_disorder": 1,
    "TMC8-related_disorder|Epidermodysplasia_verruciformis|Inborn_genetic_diseases": 1,
    "Epidermodysplasia_verruciformis|TMC8-related_disorder|Epidermodysplasia_verruciformis|_susceptibility_to|_2|not_provided|Epidermodysplasia_verruciformis|_susceptibility_to|_1": 1,
    "not_provided|not_specified|Epidermodysplasia_verruciformis|_susceptibility_to|_2": 1,
    "TMC8-related_disorder": 1,
    "PGS1-related_disorder": 1,
    "not_provided|DNAH17-related_disorder": 27,
    "DNAH17-related_disorder": 150,
    "DNAH17-related_disorder|not_specified|not_provided": 6,
    "DNAH17-related_disorder|not_provided|not_specified": 19,
    "not_specified|DNAH17-related_disorder|not_provided": 1,
    "Spermatogenic_failure_39": 17,
    "not_provided|Spermatogenic_failure_39": 1,
    "DNAH17-related_disorder|not_provided": 24,
    "Inborn_genetic_diseases|Spermatogenic_failure_39": 4,
    "Inborn_genetic_diseases|DNAH17-related_disorder": 8,
    "DNAH17-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Spermatogenic_failure_39|Inborn_genetic_diseases": 3,
    "DNAH17-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|DNAH17-related_disorder": 1,
    "not_provided|DNAH17-related_disorder|not_specified": 4,
    "DNAH17-related_disorder|not_specified": 1,
    "DNAH17-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|DNAH17-related_disorder": 1,
    "Inborn_genetic_diseases|DNAH17-related_disorder|not_provided": 3,
    "not_specified|not_provided|DNAH17-related_disorder": 1,
    "TIMP2-related_disorder": 5,
    "Desbuquois_syndrome": 2,
    "not_provided|CANT1-related_disorder|not_specified": 1,
    "CANT1-related_disorder|not_provided": 1,
    "CANT1-related_disorder|not_provided|Desbuquois_dysplasia_1": 3,
    "not_specified|not_provided|Desbuquois_dysplasia_1": 2,
    "Desbuquois_dysplasia_1|Epiphyseal_dysplasia|_multiple|_7|not_provided": 3,
    "not_provided|CANT1-related_disorder": 2,
    "Joint_dislocation|Short_stature|Desbuquois_dysplasia_1|Epiphyseal_dysplasia|_multiple|_7": 1,
    "Epiphyseal_dysplasia|_multiple|_7|Desbuquois_dysplasia_1|not_provided": 3,
    "Desbuquois_dysplasia_1|Epiphyseal_dysplasia|_multiple|_7": 2,
    "Epiphyseal_dysplasia|_multiple|_7|Desbuquois_dysplasia_1": 2,
    "not_provided|Epiphyseal_dysplasia|_multiple|_7|Desbuquois_dysplasia_1": 1,
    "not_provided|Desbuquois_dysplasia_1|Epiphyseal_dysplasia|_multiple|_7": 1,
    "Epiphyseal_dysplasia|_multiple|_7|Multiple_epiphyseal_dysplasia|not_provided": 1,
    "CANT1-related_disorder|Desbuquois_dysplasia_1|not_specified|not_provided": 1,
    "Desbuquois_dysplasia_1|Epiphyseal_dysplasia|_multiple|_7|not_specified": 1,
    "Desbuquois_dysplasia_1|not_provided|Epiphyseal_dysplasia|_multiple|_7": 1,
    "CANT1-related_disorder|Desbuquois_dysplasia_1|not_provided": 1,
    "Idiopathic_generalized_epilepsy|RBFOX3-related_disorder": 6,
    "Idiopathic_generalized_epilepsy|not_specified|RBFOX3-related_disorder": 1,
    "RBFOX3-related_disorder": 4,
    "RBFOX3-related_disorder|Idiopathic_generalized_epilepsy|not_provided": 1,
    "RBFOX3-related_disorder|not_specified|Idiopathic_generalized_epilepsy": 1,
    "RBFOX3-related_disorder|Idiopathic_generalized_epilepsy": 1,
    "46|XY_sex_reversal_5|not_provided": 1,
    "46|XY_sex_reversal_5": 5,
    "not_provided|CBX2-related_disorder": 3,
    "Pure_gonadal_dysgenesis_46|XY|CBX2-related_disorder": 1,
    "CBX2-related_disorder|not_provided": 3,
    "CBX2-related_disorder": 3,
    "Spastic_cerebral_palsy": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 33,
    "Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia": 39,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 19,
    "CCDC40-related_disorder|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 2,
    "not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 3,
    "Primary_ciliary_dyskinesia|CCDC40-related_disorder": 5,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 4,
    "not_provided|Primary_ciliary_dyskinesia_15|not_specified": 1,
    "not_provided|Primary_ciliary_dyskinesia|See_cases": 1,
    "CCDC40-related_disorder|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_15|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_specified|not_provided|Male_infertility|Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia": 1,
    "CCDC40-related_disorder": 6,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 3,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Primary_ciliary_dyskinesia_15": 1,
    "Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia|not_provided": 2,
    "Primary_ciliary_dyskinesia_15|CCDC40-related_disorder|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_15": 6,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_15": 2,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_15": 6,
    "Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_15": 3,
    "Primary_ciliary_dyskinesia|CCDC40-related_disorder|Primary_ciliary_dyskinesia_15": 1,
    "Primary_ciliary_dyskinesia_15|not_provided": 3,
    "not_provided|CCDC40-related_disorder|Primary_ciliary_dyskinesia_15": 1,
    "CCDC40-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 1,
    "CCDC40-related_disorder|Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Usher_syndrome|Primary_ciliary_dyskinesia_15": 1,
    "not_specified|Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|CCDC40-related_disorder|not_provided|Primary_ciliary_dyskinesia_15": 1,
    "Primary_ciliary_dyskinesia|Combined_immunodeficiency_due_to_DOCK8_deficiency": 1,
    "not_provided|Primary_ciliary_dyskinesia_15": 2,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia_15|sperm_axonema_without_dynein_arms_and_nexin_bridges|axonemas_with_defects_on_microtubules|not_provided": 1,
    "CCDC40-related_disorder|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_15": 1,
    "Primary_ciliary_dyskinesia|not_provided|Kartagener_syndrome|Primary_ciliary_dyskinesia_15": 1,
    "not_provided|Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia_15|not_provided|Primary_ciliary_dyskinesia|not_specified": 1,
    "Primary_ciliary_dyskinesia_15|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_15|not_specified|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia_15|not_specified|not_provided": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15|Glycogen_storage_disease|_type_II": 3,
    "Primary_ciliary_dyskinesia_15|Primary_ciliary_dyskinesia|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15|CCDC40-related_disorder": 1,
    "CCDC40-related_disorder|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_15": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15|Glycogen_storage_disease|_type_II": 1,
    "Respiratory_ciliopathies_including_non-CF_bronchiectasis|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_15|Glycogen_storage_disease|_type_II": 1,
    "not_specified|Primary_ciliary_dyskinesia_15": 1,
    "Glycogen_storage_disease|_type_II|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 3,
    "Glycogen_storage_disease|_type_II|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_15": 1,
    "Glycogen_storage_disease|_type_II|not_provided|Primary_ciliary_dyskinesia": 3,
    "Primary_ciliary_dyskinesia_15|Glycogen_storage_disease|_type_II": 1,
    "GAA-related_disorder|not_specified|Glycogen_storage_disease|_type_II": 2,
    "GAA-related_disorder": 8,
    "not_provided|Glycogen_storage_disease|_type_II": 327,
    "not_provided|Primary_ciliary_dyskinesia_15|Glycogen_storage_disease|_type_II": 1,
    "Glycogen_storage_disease_type_II|_infantile": 1,
    "GAA-related_disorder|not_provided": 2,
    "Glycogen_storage_disease|_type_II|not_specified": 8,
    "Glycogen_storage_disease_due_to_acid_maltase_deficiency|_late-onset|Cardiovascular_phenotype|POMPE_DISEASE|_LATE-ONSET|GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_IV|Myopathy|Glycogen_storage_disease|Glycogen_storage_disease|_type_II|See_cases": 1,
    "GAA-related_disorder|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Elevated_circulating_creatine_kinase_concentration|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 101,
    "Cardiovascular_phenotype|not_provided|not_specified|Glycogen_storage_disease|_type_II": 4,
    "Glycogen_storage_disease|_type_II|not_provided": 135,
    "Cardiovascular_phenotype|not_provided|Glycogen_storage_disease|_type_II": 40,
    "Cardiovascular_phenotype|Glycogen_storage_disease|_type_II|GAA-related_disorder": 2,
    "Glycogen_storage_disease|_type_II|Cardiovascular_phenotype|not_provided": 8,
    "not_specified|Glycogen_storage_disease|_type_II": 31,
    "Glycogen_storage_disease|_type_II|Cardiovascular_phenotype": 43,
    "Cardiovascular_phenotype|not_provided|Glycogen_storage_disease|_type_II|not_specified": 3,
    "not_provided|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II|Cardiomyopathy": 1,
    "GAA-related_disorder|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 5,
    "not_provided|GAA-related_disorder|Glycogen_storage_disease|_type_II": 3,
    "Glycogen_storage_disease|_type_II|not_provided|GAA-related_disorder": 2,
    "GAA-related_disorder|not_specified|Glycogen_storage_disease|_type_II|not_provided": 4,
    "Cardiovascular_phenotype|not_specified|not_provided|Glycogen_storage_disease|_type_II": 21,
    "not_specified|not_provided|Glycogen_storage_disease|_type_II": 25,
    "Cardiovascular_phenotype|not_specified|not_provided|Acid_alpha-glucosidase|_allele_2|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 20,
    "GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_II|Glycogen_storage_disease": 2,
    "Glycogen_storage_disease|_type_II|GAA-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_II": 3,
    "Cardiovascular_phenotype|not_specified|not_provided|Primary_ciliary_dyskinesia|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|GAA-related_disorder|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Long_QT_syndrome|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Primary_dilated_cardiomyopathy|not_specified|GAA-related_disorder|Glycogen_storage_disease|_type_II": 1,
    "not_specified|Glycogen_storage_disease|_type_II|not_provided": 5,
    "POMPE_DISEASE|_LATE-ONSET|not_provided|Glycogen_storage_disease|_type_II|See_cases": 1,
    "not_provided|not_specified|Glycogen_storage_disease|_type_II": 17,
    "GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_II": 8,
    "Cardiovascular_phenotype|not_specified|Glycogen_storage_disease|_type_II": 3,
    "GAA-related_disorder|not_specified|not_provided|Glycogen_storage_disease|_type_II": 3,
    "not_specified|Cardiovascular_phenotype|not_provided|GAA-related_disorder|Glycogen_storage_disease|_type_II|Ventricular_fibrillation": 1,
    "GAA-related_disorder|POMPE_DISEASE|_LATE-ONSET|not_specified|not_provided|Glycogen_storage_disease|_type_II": 1,
    "GAA-related_disorder|not_provided|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|Glycogen_storage_disease|_type_II|not_provided": 7,
    "Cardiovascular_phenotype|not_specified|Glycogen_storage_disease|_type_II|not_provided": 5,
    "not_specified|Cardiovascular_phenotype|not_provided|Glycogen_storage_disease|_type_II": 1,
    "GAA-related_disorder|Cardiovascular_phenotype|not_provided|Glycogen_storage_disease|_type_II": 3,
    "not_provided|Glycogen_storage_disease|_type_II|not_specified": 9,
    "not_provided|Glycogen_storage_disease|_type_II|Cardiovascular_phenotype": 9,
    "not_provided|Metabolic_myopathy|not_specified|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Glycogen_storage_disease|_type_II": 3,
    "POMPE_DISEASE|_LATE-ONSET|not_provided|Glycogen_storage_disease|_type_II": 4,
    "Glycogen_storage_disease|_type_II|not_provided|Cardiovascular_phenotype": 6,
    "not_provided|Cardiomyopathy|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|Glycogen_storage_disease|_type_II|not_specified|not_provided": 2,
    "not_specified|not_provided|See_cases|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 1,
    "Glycogen_storage_disease|_type_II|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|GAA-related_disorder|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|not_provided|GAA-related_disorder|Glycogen_storage_disease|_type_II": 3,
    "POMPE_DISEASE|_LATE-ONSET|Glycogen_storage_disease|_type_II": 2,
    "not_specified|not_provided|Glycogen_storage_disease|_type_II|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 5,
    "GAA-related_disorder|Glycogen_storage_disease|_type_II": 3,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_specified|GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Glycogen_storage_disease|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|GAA-related_disorder|not_specified|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Cardiovascular_phenotype|GAA-related_disorder|not_specified|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Glycogen_storage_disease|_type_II|GAA-related_disorder": 1,
    "not_specified|GAA-related_disorder|Glycogen_storage_disease|_type_II": 1,
    "Glycogen_storage_disease|_type_II|GAA-related_disorder": 2,
    "Cardiovascular_phenotype|GAA-related_disorder|not_specified|not_provided|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Glycogen_storage_disease|_type_II|Cardiovascular_phenotype|not_specified": 1,
    "GAA-related_disorder|not_provided|not_specified|Glycogen_storage_disease|_type_II": 1,
    "GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_II|Cardiovascular_phenotype": 1,
    "not_provided|POMPE_DISEASE|_LATE-ONSET|Glycogen_storage_disease|_type_II": 1,
    "Glycogen_storage_disease|_type_II|Glycogen_storage_disease_due_to_glucose-6-phosphatase_deficiency_type_IA|not_provided": 1,
    "Glycogen_storage_disease|_type_II|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease|_type_II": 1,
    "Glycoprotein_storage_disease|Glycogen_storage_disease|_type_II|not_provided": 1,
    "Glycogen_storage_disease|_type_II|Rare_genetic_deafness|not_provided": 1,
    "not_provided|Glycogen_storage_disease|_type_II|Abnormality_of_metabolism/homeostasis": 1,
    "not_provided|GAA-related_disorder|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 1,
    "GAA-related_disorder|Cardiovascular_phenotype|not_specified|Glycogen_storage_disease|_type_II": 1,
    "Glycogen_storage_disease|_type_II|not_specified|GAA-related_disorder|not_provided": 1,
    "not_provided|GAA-related_disorder|not_specified|Glycogen_storage_disease|_type_II": 2,
    "Glycogen_storage_disease|_type_II|POMPE_DISEASE|_LATE-ONSET": 3,
    "GAA-related_disorder|Glycogen_storage_disease|_type_II|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Acid_alpha-glucosidase|_allele_4|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|GAA-related_disorder|Glycogen_storage_disease|_type_II": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Glycogen_storage_disease|_type_II|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II|not_provided": 2,
    "not_specified|GAA-related_disorder|not_provided|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 1,
    "not_provided|Glycogen_storage_disease|Cardiovascular_phenotype|GAA-related_disorder|Glycogen_storage_disease|_type_II": 1,
    "Glycogen_storage_disease|_type_II|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II": 1,
    "not_specified|not_provided|Glycogen_storage_disease|_type_II|See_cases": 1,
    "not_provided|Glycogen_storage_disease|_type_II|Glycogen_storage_disease": 1,
    "not_provided|not_specified|Glycogen_storage_disease|_type_II|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|POMPE_DISEASE|_LATE-ONSET|GAA-related_disorder|not_provided|Glycogen_storage_disease|_type_II": 1,
    "Cardiovascular_phenotype|GAA-related_disorder|Glycogen_storage_disease|_type_II|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Glycogen_storage_disease|_type_II|Hypertrophic_cardiomyopathy": 1,
    "GAA-related_disorder|Cardiovascular_phenotype|Glycogen_storage_disease|_type_II|not_provided": 1,
    "not_provided|EIF4A3-related_disorder": 1,
    "EIF4A3-related_disorder": 3,
    "Richieri_Costa-Pereira_syndrome": 1,
    "Autoinflammatory_syndrome|CARD14-related_disorder": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2": 658,
    "not_provided|Pityriasis_rubra_pilaris|Psoriasis_2": 15,
    "Inborn_genetic_diseases|not_provided|Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Inborn_genetic_diseases": 43,
    "CARD14-related_disorder|Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2": 2,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome": 13,
    "Psoriasis_2|Pityriasis_rubra_pilaris": 163,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 27,
    "Autoinflammatory_syndrome|Psoriasis_2|Pityriasis_rubra_pilaris": 3,
    "Psoriasis_2|Pityriasis_rubra_pilaris|CARD14-related_disorder": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|Inborn_genetic_diseases": 7,
    "Autoinflammatory_syndrome|CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 4,
    "Autoinflammatory_syndrome|not_provided|Pityriasis_rubra_pilaris|Psoriasis_2": 11,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome|Inborn_genetic_diseases": 3,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_specified|not_provided|CARD14-related_disorder|Autoinflammatory_syndrome": 1,
    "not_provided|Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome": 3,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 11,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2": 19,
    "CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome": 2,
    "CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2": 8,
    "Psoriasis_2|not_provided|Pityriasis_rubra_pilaris|Papulosquamous_eruptions": 1,
    "Psoriasis_2": 1,
    "Papulosquamous_eruptions|Pityriasis_rubra_pilaris": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|not_provided": 4,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Papulosquamous_eruptions": 2,
    "Papulosquamous_eruptions": 3,
    "Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2": 30,
    "not_specified|Autoinflammatory_syndrome|not_provided|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "Papulosquamous_eruptions|not_provided": 1,
    "PSORIASIS_2|_PUSTULAR|not_provided": 1,
    "Psoriasis_2|not_provided": 2,
    "Inborn_genetic_diseases|Psoriasis_2|Pityriasis_rubra_pilaris": 8,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|CARD14-related_disorder|Inborn_genetic_diseases": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|Papulosquamous_eruptions|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Psoriasis_2|Pityriasis_rubra_pilaris": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Inborn_genetic_diseases|Autoinflammatory_syndrome": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_provided|Autoinflammatory_syndrome": 5,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Pityriasis_rubra_pilaris|Psoriasis_2|not_specified": 3,
    "Pityriasis_rubra_pilaris|Psoriasis_2|CARD14-related_disorder": 5,
    "not_provided|not_specified|Pityriasis_rubra_pilaris|Psoriasis_2": 2,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_specified": 1,
    "not_provided|Psoriasis_2|Pityriasis_rubra_pilaris|not_specified": 2,
    "Psoriasis_2|Pityriasis_rubra_pilaris|not_provided|Autoinflammatory_syndrome": 1,
    "not_specified|Psoriasis_2|Pityriasis_rubra_pilaris": 1,
    "Autoinflammatory_syndrome|not_provided|CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Pityriasis_rubra_pilaris|Psoriasis_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 3,
    "Autoinflammatory_syndrome|CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2": 2,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome|not_provided": 7,
    "not_provided|Psoriasis_2|Pityriasis_rubra_pilaris": 1,
    "Psoriasis_2|Autoinflammatory_syndrome|Inborn_genetic_diseases|Pityriasis_rubra_pilaris": 1,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2|CARD14-related_disorder": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_specified|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 1,
    "Autoinflammatory_syndrome|not_provided|CARD14-related_disorder|not_specified|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "not_provided|Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2": 3,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Inborn_genetic_diseases|CARD14-related_disorder|Autoinflammatory_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "not_provided|CARD14-related_disorder|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "CARD14-related_disorder": 8,
    "Pityriasis_rubra_pilaris|Psoriasis_2|not_provided|not_specified": 1,
    "CARD14-related_disorder|Autoinflammatory_syndrome|not_provided|Pityriasis_rubra_pilaris|Psoriasis_2": 2,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Inborn_genetic_diseases|CARD14-related_disorder": 1,
    "Familial_pityriasis_rubra_pilaris": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|Inborn_genetic_diseases|Autoinflammatory_syndrome": 1,
    "not_specified|Psoriasis_2|Pityriasis_rubra_pilaris|not_provided": 3,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2|not_specified|not_provided": 1,
    "Autoinflammatory_syndrome|not_provided|Pityriasis_rubra_pilaris|Psoriasis_2|not_specified": 1,
    "Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided|Autoinflammatory_syndrome": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|CARD14-related_disorder|not_provided": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|Inborn_genetic_diseases|not_provided": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome|not_provided|CARD14-related_disorder": 2,
    "CARD14-related_disorder|Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2|not_specified": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|not_provided|not_specified": 1,
    "Pityriasis_rubra_pilaris|not_provided|not_specified|Psoriasis_2": 1,
    "not_specified|not_provided|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "Autoinflammatory_syndrome|not_specified|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided": 1,
    "Psoriasis_2|Pityriasis_rubra_pilaris|Autoinflammatory_syndrome": 2,
    "CARD14-related_disorder|not_specified|not_provided|Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2": 1,
    "Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2": 2,
    "Autoinflammatory_syndrome|Pityriasis_rubra_pilaris|Psoriasis_2|not_provided|CARD14-related_disorder": 1,
    "Pityriasis_rubra_pilaris|Psoriasis_2|CARD14-related_disorder|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pityriasis_rubra_pilaris|Psoriasis_2|Autoinflammatory_syndrome|not_provided": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_provided": 30,
    "Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases": 24,
    "Mucopolysaccharidosis|_MPS-III-A|SGSH-related_disorder": 6,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A": 33,
    "not_provided|not_specified|Mucopolysaccharidosis|_MPS-III-A": 2,
    "SGSH-related_disorder|not_provided|Mucopolysaccharidosis|_MPS-III-A": 4,
    "Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis|_MPS-III-A": 3,
    "Mucopolysaccharidosis|_MPS-III-A|SGSH-related_disorder|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases|Sanfilippo_syndrome": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A": 12,
    "not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A": 3,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A|SGSH-related_disorder": 1,
    "Developmental_regression|Severely_reduced_visual_acuity|Nystagmus|Diarrhea|Retinal_dystrophy|Global_developmental_delay|Gastrointestinal_dysmotility|Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis|_MPS-III-A|Cone-rod_dystrophy": 1,
    "Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A|not_provided": 3,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A|not_specified": 2,
    "not_specified|not_provided|Mucopolysaccharidosis|_MPS-III-A": 4,
    "Intellectual_disability|Mucopolysaccharidosis|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Sanfilippo_syndrome|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_specified|not_provided": 6,
    "Mucopolysaccharidosis|_MPS-III-A|not_provided|Mucopolysaccharidosis": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-A": 9,
    "Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-A|not_provided|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_specified|SGSH-related_disorder": 1,
    "SGSH-related_disorder|Mucopolysaccharidosis|_MPS-III-A": 5,
    "SGSH-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_specified": 3,
    "Developmental_regression|Gastrointestinal_dysmotility|Retinal_dystrophy|Nystagmus|Diarrhea|Global_developmental_delay|Severely_reduced_visual_acuity|Sanfilippo_syndrome|Neurodegeneration|Inborn_genetic_diseases|Mucopolysaccharidosis|not_provided|Mucopolysaccharidosis|_MPS-III-A|Cone-rod_dystrophy": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_provided|Inborn_genetic_diseases": 1,
    "SGSH-related_disorder|Inborn_genetic_diseases|Sanfilippo_syndrome|Neurodegeneration|Mucopolysaccharidosis|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "not_provided|SGSH-related_disorder|Mucopolysaccharidosis|_MPS-III-A": 2,
    "not_specified|not_provided|SGSH-related_disorder|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Inborn_genetic_diseases|not_provided|Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_provided|SGSH-related_disorder": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_provided|not_specified": 2,
    "not_specified|Mucopolysaccharidosis|_MPS-III-A|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SGSH-related_disorder|Mucopolysaccharidosis|_MPS-III-A": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-III-A|Intellectual_disability": 2,
    "not_provided|SGSH-related_disorder|not_specified|Mucopolysaccharidosis|_MPS-III-A": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A|Abnormality_of_metabolism/homeostasis": 1,
    "SGSH-related_disorder|Mucopolysaccharidosis|_MPS-III-A|not_provided": 2,
    "not_provided|Mucopolysaccharidosis|Mucopolysaccharidosis|_MPS-III-A|Abnormal_circulating_carbohydrate_concentration": 1,
    "SGSH-related_disorder|Inborn_genetic_diseases|Sanfilippo_syndrome|Mucopolysaccharidosis|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "See_cases|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Sanfilippo_syndrome|Mucopolysaccharidosis|_MPS-III-A": 2,
    "Stroke_disorder|Seizure|Inguinal_hernia|Hemangioma|Nephrocalcinosis": 1,
    "RNF213-related_disorder": 30,
    "Moyamoya_disease_2|RNF213-related_disorder|not_provided": 2,
    "not_provided|Moyamoya_disease_2": 12,
    "not_provided|RNF213-related_disorder": 26,
    "RNF213-related_disorder|not_provided|Moyamoya_disease_2": 2,
    "RNF213-related_disorder|not_provided": 27,
    "Moyamoya_disease_2|not_provided": 11,
    "RNF213-related_disorder|Moyamoya_disease_2|not_provided": 1,
    "Atypical_coarctation_of_aorta|not_provided|Moyamoya_disease_2": 1,
    "Patent_foramen_ovale|Coronary_artery_disorder|Middle_cerebral_artery_stenosis|Stroke_disorder|Atrial_septal_dilatation|Carotid_artery_stenosis|See_cases": 1,
    "RNF213-related_disorder|not_provided|not_specified": 1,
    "not_provided|Moyamoya_disease": 1,
    "Moyamoya_angiopathy|Moyamoya_disease_2": 1,
    "Moyamoya_disease_2|Moyamoya_disease_1|not_provided": 1,
    "Moyamoya_disease|not_provided": 1,
    "Moyamoya_disease_2|Moyamoya_angiopathy": 1,
    "Anaplastic_ependymoma": 1,
    "not_provided|RNF213-related_disorder|Moyamoya_disease_2": 1,
    "not_provided|Moyamoya_disease_2|See_cases": 1,
    "Moyamoya_disease_2|not_provided|Inborn_genetic_diseases": 1,
    "Moyamoya_disease_2|RNF213-related_disorder": 1,
    "UMLS:_C0007644": 1,
    "Spinocerebellar_ataxia_50": 6,
    "Spinocerebellar_ataxia_50|not_provided|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_34": 1,
    "Mitochondrial_disease|Mitochondrial_complex_I_deficiency|_nuclear_type_34": 3,
    "NDUFAF8-related_disorder": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_34|NDUFAF8-related_disorder|not_provided|Mitochondrial_disease": 1,
    "SLC38A10-related_disorder": 7,
    "not_provided|ACTG1-related_disorder": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_specified": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 75,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 163,
    "ACTG1-related_disorder": 12,
    "not_provided|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_specified": 2,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_specified": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20": 13,
    "not_provided|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 17,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 16,
    "not_specified|ACTG1-related_disorder|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 2,
    "ACTG1-related_disorder|not_specified": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided": 15,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_provided": 2,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 3,
    "ACTG1-related_disorder|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_specified|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided|Baraitser-winter_syndrome_2": 3,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_delay|Baraitser-winter_syndrome_2": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20": 4,
    "Baraitser-winter_syndrome_2": 12,
    "not_specified|not_provided|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|ACTG1-related_disorder|not_specified|not_provided": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided|not_specified": 4,
    "ACTG1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_specified|Intellectual_disability|not_provided|ACTG1-related_disorder": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided|ACTG1-related_disorder": 1,
    "not_specified|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_provided|not_specified": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|not_specified|not_provided|Baraitser-winter_syndrome_2": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|ACTG1-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_provided": 16,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_specified": 4,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|ACTG1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 4,
    "ACTG1-related_disorder|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_specified|not_provided": 6,
    "Baraitser-winter_syndrome_2|Lissencephaly|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|ACTG1-related_disorder": 1,
    "Baraitser-winter_syndrome_2|not_provided": 1,
    "Hearing_impairment|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided|Rare_genetic_deafness": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_specified|not_provided": 5,
    "not_specified|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 7,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|Inborn_genetic_diseases": 1,
    "Baraitser-winter_syndrome_2|ACTG1-related_disorder|Inborn_genetic_diseases": 1,
    "ACTG1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_specified|not_provided": 7,
    "Microcephaly|Baraitser-winter_syndrome_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_provided|ACTG1-related_disorder": 2,
    "Baraitser-winter_syndrome_2|Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_20": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|ACTG1-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|ACTG1-related_disorder|not_provided": 2,
    "not_provided|Baraitser-winter_syndrome_2": 2,
    "ACTG1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_provided": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-Winter_syndrome": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|ACTG1-related_disorder": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|ACTG1-related_disorder|Baraitser-winter_syndrome_2|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|ACTG1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20": 1,
    "not_provided|not_specified|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 1,
    "Baraitser-winter_syndrome_2|Inborn_genetic_diseases|not_provided|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|not_provided|not_specified|ACTG1-related_disorder": 1,
    "See_cases|not_provided|Baraitser-winter_syndrome_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided|Baraitser-winter_syndrome_2|not_specified": 2,
    "not_provided|ACTG1-related_disorder|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20": 1,
    "not_provided|ACTG1-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 1,
    "Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_specified|not_provided|ACTG1-related_disorder": 1,
    "Baraitser-winter_syndrome_2|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided": 1,
    "Intellectual_disability|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|not_provided": 1,
    "not_specified|Baraitser-winter_syndrome_2|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20": 1,
    "not_provided|Baraitser-winter_syndrome_2|Autosomal_dominant_nonsyndromic_hearing_loss_20|ACTG1-related_disorder": 1,
    "ACTG1-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ACTG1-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_20|Baraitser-winter_syndrome_2": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_20|ACTG1-related_disorder": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_30": 2,
    "Macular_degeneration|Leber_congenital_amaurosis|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_30": 1,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_30": 1,
    "Retinal_dystrophy|not_specified|not_provided|Retinitis_pigmentosa_30": 1,
    "not_provided|FSCN2-related_disorder": 7,
    "Retinitis_pigmentosa_30|not_specified|not_provided": 1,
    "Retinal_dystrophy|not_provided|not_specified|Retinitis_pigmentosa_30": 1,
    "FSCN2-related_disorder|not_provided": 4,
    "FSCN2-related_disorder": 2,
    "not_provided|Retinal_dystrophy|FSCN2-related_disorder": 1,
    "FSCN2-related_disorder|Retinitis_pigmentosa_30|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_30|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_30|not_provided": 4,
    "Retinitis_pigmentosa_30|not_provided|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_30|not_specified": 1,
    "Retinitis_pigmentosa_30": 2,
    "FSCN2-related_disorder|not_provided|not_specified": 1,
    "FANCONI_ANEMIA|_COMPLEMENTATION_GROUP_X": 3,
    "Retinitis_pigmentosa_57|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_57|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_57": 1,
    "MRPL12-related_disorder|not_specified": 1,
    "Combined_oxidative_phosphorylation_deficiency_45": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_DNA_depletion_syndrome_19": 1,
    "Mitochondrial_DNA_depletion_syndrome_19": 2,
    "SLC25A10-related_disorder|Mitochondrial_DNA_depletion_syndrome_19|not_provided": 1,
    "GCGR-related_disorder": 3,
    "not_provided|GCGR-related_hyperglucagonemia": 1,
    "GCGR-related_hyperglucagonemia": 6,
    "not_provided|GCGR-related_disorder": 5,
    "GCGR-related_disorder|not_provided": 2,
    "GCGR-related_hyperglucagonemia|not_provided": 1,
    "not_provided|P4HB-related_disorder": 6,
    "Cole-Carpenter_syndrome_1": 8,
    "P4HB-related_disorder|not_provided": 4,
    "P4HB-related_disorder": 6,
    "Cole-Carpenter_syndrome": 1,
    "not_provided|Cole-Carpenter_syndrome_1": 2,
    "not_provided|Inborn_genetic_diseases|Cole-Carpenter_syndrome_1": 1,
    "P4HB-related_disorder|Cole-Carpenter_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|P4HB-related_disorder|not_provided": 1,
    "ARHGDIA-related_disorder": 11,
    "Nephrotic_syndrome|_type_8": 7,
    "ARHGDIA-related_disorder|Nephrotic_syndrome|_type_8|not_provided|Chronic_kidney_disease": 1,
    "not_provided|ARHGDIA-related_disorder": 1,
    "not_provided|Nephrotic_syndrome|_type_8": 1,
    "ALYREF-related_disorder": 3,
    "Spastic_paraplegia_82|_autosomal_recessive|Inborn_genetic_diseases": 2,
    "Spastic_paraplegia_82|_autosomal_recessive": 12,
    "Spastic_paraplegia_82|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Spastic_paraplegia_82|_autosomal_recessive": 1,
    "not_provided|Cutis_laxa": 6,
    "PYCR1-related_disorder": 3,
    "not_provided|Cutis_laxa|Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome": 1,
    "Cutis_laxa|not_provided": 10,
    "Autosomal_recessive_cutis_laxa_type_2B|not_provided|not_specified": 1,
    "Cutis_laxa|Inborn_genetic_diseases": 1,
    "not_provided|PYCR1-related_disorder": 7,
    "not_specified|Cutis_laxa|not_provided": 2,
    "Autosomal_recessive_cutis_laxa_type_2B|not_specified|not_provided": 1,
    "PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B": 5,
    "not_provided|Autosomal_recessive_cutis_laxa_type_2B|Inborn_genetic_diseases|Cutis_laxa": 1,
    "not_provided|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B|Inborn_genetic_diseases": 1,
    "PYCR1-related_de_Barsy_syndrome": 1,
    "Inborn_genetic_diseases|Wiedemann-Rautenstrauch-like_progeroid_syndrome|Cutis_laxa|not_provided|PYCR1-related_de_Barsy_syndrome": 1,
    "not_provided|Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome": 1,
    "Cutis_laxa|Inborn_genetic_diseases|PYCR1-related_de_Barsy_syndrome|not_provided": 1,
    "Autosomal_recessive_cutis_laxa_type_2B|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|not_provided|PYCR1-related_de_Barsy_syndrome": 1,
    "Autosomal_recessive_cutis_laxa_type_2B|not_provided": 3,
    "not_specified|Autosomal_recessive_cutis_laxa_type_2B": 1,
    "Autosomal_recessive_cutis_laxa_type_2B": 13,
    "PYCR1-related_disorder|Wiedemann-Rautenstrauch-like_progeroid_syndrome|Inborn_genetic_diseases|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B|not_provided|Cutis_laxa": 1,
    "Autosomal_recessive_cutis_laxa_type_2B|Cutis_laxa|PYCR1-related_de_Barsy_syndrome|not_provided|Abnormality_of_connective_tissue": 1,
    "Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome|not_provided": 1,
    "Wiedemann-Rautenstrauch-like_progeroid_syndrome|Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome|not_provided": 1,
    "PYCR1-related_disorder|not_provided": 2,
    "Cutis_laxa|not_provided|Wiedemann-Rautenstrauch-like_progeroid_syndrome|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B": 1,
    "Inborn_genetic_diseases|Cutis_laxa|not_provided|Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome": 1,
    "Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome": 1,
    "Wiedemann-Rautenstrauch-like_progeroid_syndrome|PYCR1-related_disorder|Cutis_laxa|not_provided|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B": 1,
    "PYCR1-related_disorder|Cutis_laxa|not_provided|Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome": 1,
    "not_specified|PYCR1-related_disorder|Cutis_laxa|not_provided": 1,
    "PYCR1-related_de_Barsy_syndrome|not_provided": 1,
    "PYCR1-related_disorder|Cutis_laxa|not_provided|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B": 1,
    "not_provided|Cutis_laxa|Microcephaly": 1,
    "Cutis_laxa|PYCR1-related_disorder|not_provided": 1,
    "PYCR1-related_disorder|Wiedemann-Rautenstrauch-like_progeroid_syndrome": 1,
    "Cutis_laxa|PYCR1-related_de_Barsy_syndrome|Inborn_genetic_diseases": 1,
    "Cutis_laxa|not_provided|PYCR1-related_disorder": 1,
    "PYCR1-related_disorder|not_provided|not_specified|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B": 1,
    "Autosomal_recessive_cutis_laxa_type_2B|PYCR1-_related_autosomal_recessive_cutis_laxa": 1,
    "PYCR1-related_disorder|PYCR1-related_de_Barsy_syndrome|Autosomal_recessive_cutis_laxa_type_2B|not_provided|Cutis_laxa": 1,
    "PYCR1-related_disorder|Autosomal_recessive_cutis_laxa_type_2B|PYCR1-related_de_Barsy_syndrome": 1,
    "LRRC45-related_disorder": 46,
    "LRRC45-related_disorder|not_specified": 6,
    "not_specified|LRRC45-related_disorder": 12,
    "LRRC45_associated_neurological_ciliopathy": 1,
    "Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies": 8,
    "not_provided|RAC3-related_disorder": 2,
    "Abnormal_brain_morphology|Intellectual_disability|Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies": 1,
    "RAC3-related_disorder": 9,
    "Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies|not_provided|Distal_shortening_of_limbs": 1,
    "Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies|Abnormal_brain_morphology|Intellectual_disability": 1,
    "not_provided|See_cases|Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies": 1,
    "not_provided|Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies": 2,
    "Neurodevelopmental_disorder_with_structural_brain_anomalies_and_dysmorphic_facies|Inborn_genetic_diseases": 1,
    "DCXR-related_disorder": 4,
    "Essential_pentosuria|DCXR-related_disorder": 1,
    "Essential_pentosuria": 1,
    "Microcephaly|Neurodevelopmental_delay|Seizure": 1,
    "Epileptic_encephalopathy|FASN-related_disorder": 25,
    "FASN-related_disorder|not_provided|Epileptic_encephalopathy": 5,
    "FASN-related_disorder": 14,
    "FASN-related_disorder|Epileptic_encephalopathy|not_provided": 3,
    "FASN-related_disorder|Epileptic_encephalopathy": 14,
    "Epileptic_encephalopathy|FASN-related_disorder|not_specified": 1,
    "Epileptic_encephalopathy|FASN-related_disorder|not_provided": 13,
    "not_specified|not_provided|Epileptic_encephalopathy": 4,
    "FASN-related_disorder|not_specified|Epileptic_encephalopathy": 1,
    "Epileptic_encephalopathy|not_specified|FASN-related_disorder": 1,
    "not_provided|FASN-related_disorder|Epileptic_encephalopathy": 2,
    "not_provided|Epileptic_encephalopathy|FASN-related_disorder": 1,
    "Autism_spectrum_disorder|Epileptic_encephalopathy": 1,
    "FASN-associated_disorder": 1,
    "Epileptic_encephalopathy|not_provided|FASN-related_disorder": 1,
    "Midface_retrusion|Clinodactyly|Thrombocytopenia|Abnormal_facial_shape|Hearing_impairment|Finger_clinodactyly|Tremor|Esotropia": 1,
    "not_specified|FASN-related_disorder|Epileptic_encephalopathy": 1,
    "CSNK1D-related_disorder": 7,
    "Advanced_sleep_phase_syndrome_2": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_5": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_5|not_provided": 1,
    "Neurodevelopmental_disorder_with_spastic_quadriplegia_and_brain_abnormalities_with_or_without_seizures|not_provided": 3,
    "Neurodevelopmental_disorder_with_spastic_quadriplegia_and_brain_abnormalities_with_or_without_seizures": 5,
    "not_provided|Neurodevelopmental_disorder_with_spastic_quadriplegia_and_brain_abnormalities_with_or_without_seizures": 1,
    "WDR45B-related_disorder": 1,
    "not_provided|WDR45B-related_disorder": 1,
    "not_provided|TBCD-related_disorder": 10,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 51,
    "not_provided|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 22,
    "Inborn_genetic_diseases|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_provided": 2,
    "TBCD-related_disorder|not_provided": 14,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_provided": 19,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|TBCD-related_disorder|not_provided": 2,
    "not_specified|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|TBCD-related_disorder|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "not_specified|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|TBCD-related_disorder|not_provided": 1,
    "Seborrhea-like_dermatitis_with_psoriasiform_elements": 4,
    "Seborrhea-like_dermatitis_with_psoriasiform_elements|not_specified": 1,
    "not_provided|not_specified|ZNF750-related_disorder": 1,
    "not_provided|ZNF750-related_disorder": 1,
    "ZNF750-related_disorder": 5,
    "ZNF750-related_disorder|not_provided": 2,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "TBCD-related_disorder|not_specified|not_provided": 1,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|Inborn_genetic_diseases": 4,
    "TBCD-related_disorder|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_provided": 1,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|Thiel-Behnke_corneal_dystrophy": 1,
    "Inborn_genetic_diseases|TBCD-related_disorder|not_provided|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "TBCD-related_disorder|not_provided|Inborn_genetic_diseases|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "TBCD-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "TBCD-related_disorder": 1,
    "Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome|TBCD-related_disorder": 1,
    "Thiel-Behnke_corneal_dystrophy|not_provided|TBCD-related_disorder|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "not_specified|not_provided|Early-onset_progressive_diffuse_brain_atrophy-microcephaly-muscle_weakness-optic_atrophy_syndrome": 1,
    "See_cases|not_provided|Distal_arthrogryposis_and_CNS_involvement": 1,
    "Hearing_loss|_autosomal_dominant_86": 2,
    "TYMS-related_disorder|not_provided": 1,
    "TYMS-related_disorder": 2,
    "Dyskeratosis_congenita|_digenic|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_digenic": 3,
    "Facioscapulohumeral_muscular_dystrophy_2": 839,
    "Inborn_genetic_diseases|Facioscapulohumeral_muscular_dystrophy_2": 20,
    "Facioscapulohumeral_muscular_dystrophy_2|Inborn_genetic_diseases|not_provided|SMCHD1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Facioscapulohumeral_muscular_dystrophy_2": 18,
    "not_provided|Facioscapulohumeral_muscular_dystrophy_2": 82,
    "not_specified|Facioscapulohumeral_muscular_dystrophy_2": 5,
    "Scapulohumeral_muscular_dystrophy": 9,
    "not_provided|Inborn_genetic_diseases|Facioscapulohumeral_muscular_dystrophy_2": 5,
    "Facioscapulohumeral_muscular_dystrophy_2|not_provided": 70,
    "SMCHD1-related_disorder|not_provided|Facioscapulohumeral_muscular_dystrophy_2": 3,
    "not_specified|Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|not_provided": 3,
    "Facioscapulohumeral_muscular_dystrophy_2|SMCHD1-related_disorder": 4,
    "Facioscapulohumeral_muscular_dystrophy_2|Inborn_genetic_diseases": 19,
    "Facioscapulohumeral_muscular_dystrophy_2|not_specified": 7,
    "Muscle_weakness|Facioscapulohumeral_muscular_dystrophy_2": 1,
    "not_provided|not_specified|Facioscapulohumeral_muscular_dystrophy_2": 4,
    "not_specified|Facioscapulohumeral_muscular_dystrophy_2|not_provided": 4,
    "Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 17,
    "SMCHD1-related_disorder|not_specified|not_provided|Facioscapulohumeral_muscular_dystrophy_2": 1,
    "not_specified|not_provided|Facioscapulohumeral_muscular_dystrophy_2": 6,
    "SMCHD1-related_disorder|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 1,
    "not_provided|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 4,
    "Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 4,
    "not_provided|SMCHD1-related_disorder|not_specified|Facioscapulohumeral_muscular_dystrophy_2": 2,
    "SMCHD1-related_disorder": 9,
    "Inborn_genetic_diseases|not_specified|not_provided|Facioscapulohumeral_muscular_dystrophy_2": 1,
    "Cryptorchidism|Short_nose|Microphallus|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 1,
    "Scapulohumeral_muscular_dystrophy|Facioscapulohumeral_muscular_dystrophy_2": 2,
    "Facioscapulohumeral_muscular_dystrophy_2|Inborn_genetic_diseases|not_provided": 7,
    "not_specified|Facioscapulohumeral_muscular_dystrophy_2|Inborn_genetic_diseases": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|not_provided|Inborn_genetic_diseases": 3,
    "Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|Anosmia": 1,
    "Inborn_genetic_diseases|Facioscapulohumeral_muscular_dystrophy_2|not_provided": 3,
    "Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|Facioscapulohumeral_muscular_dystrophy_2": 3,
    "Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|not_provided": 2,
    "Short_nose|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|Anosmia": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Weakness_of_facial_musculature": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|See_cases": 1,
    "Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|not_provided": 2,
    "SMCHD1-related_disorder|not_provided": 2,
    "SMCHD1-related_disorder|Facioscapulohumeral_muscular_dystrophy_2": 2,
    "not_provided|Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|SMCHD1-related_disorder|not_provided": 2,
    "not_specified|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|not_provided|Facioscapulohumeral_muscular_dystrophy_2": 4,
    "not_provided|Facioscapulohumeral_muscular_dystrophy_2|not_specified": 4,
    "Facioscapulohumeral_muscular_dystrophy_2|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "not_provided|SMCHD1-related_disorder|Facioscapulohumeral_muscular_dystrophy_2": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|not_provided|not_specified": 3,
    "Facioscapulohumeral_muscular_dystrophy_2|SMCHD1-related_disorder|not_provided|not_specified": 1,
    "not_provided|Facioscapulohumeral_muscular_dystrophy_2|Inborn_genetic_diseases": 3,
    "not_specified|Scapulohumeral_muscular_dystrophy|Facioscapulohumeral_muscular_dystrophy_2|not_provided": 1,
    "SMCHD1-related_disorder|Facioscapulohumeral_muscular_dystrophy_2|not_provided": 1,
    "not_specified|not_provided|Facioscapulohumeral_muscular_dystrophy_2|Inborn_genetic_diseases": 1,
    "Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|Facioscapulohumeral_muscular_dystrophy_2|not_provided": 1,
    "Muscular_atrophy": 2,
    "Facioscapulohumeral_muscular_dystrophy_2|Shoulder_girdle_muscle_weakness": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|not_provided|SMCHD1-related_disorder": 1,
    "not_provided|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|Facioscapulohumeral_muscular_dystrophy_2": 1,
    "Proximal_muscle_weakness_in_upper_limbs": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|Scapular_winging": 1,
    "Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome|SMCHD1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Facioscapulohumeral_muscular_dystrophy_2|Arrhinia_with_choanal_atresia_and_microphthalmia_syndrome": 1,
    "Majeed_syndrome": 618,
    "Majeed_syndrome|not_provided": 22,
    "not_provided|Majeed_syndrome": 23,
    "not_provided|Autoinflammatory_syndrome|Majeed_syndrome": 2,
    "not_provided|Majeed_syndrome|Autoinflammatory_syndrome": 3,
    "Majeed_syndrome|Autoinflammatory_syndrome|not_provided": 5,
    "not_specified|not_provided|Majeed_syndrome|Autoinflammatory_syndrome": 1,
    "LPIN2-related_disorder": 1,
    "Majeed_syndrome|Autoinflammatory_syndrome": 5,
    "Majeed_syndrome|LPIN2-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "Majeed_syndrome|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Majeed_syndrome": 13,
    "not_specified|Majeed_syndrome": 17,
    "LPIN2-related_disorder|Autoinflammatory_syndrome|not_provided|Majeed_syndrome": 3,
    "Majeed_syndrome|Inborn_genetic_diseases": 12,
    "Autoinflammatory_syndrome|Majeed_syndrome|not_provided": 2,
    "LPIN2-related_disorder|Autoinflammatory_syndrome|Majeed_syndrome": 1,
    "LPIN2-related_disorder|not_specified|Autoinflammatory_syndrome|Majeed_syndrome": 1,
    "Majeed_syndrome|not_specified": 7,
    "not_provided|Majeed_syndrome|LPIN2-related_disorder|Autoinflammatory_syndrome": 1,
    "Majeed_syndrome|not_provided|LPIN2-related_disorder|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_specified|Majeed_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Majeed_syndrome": 5,
    "Majeed_syndrome|Autoinflammatory_syndrome|not_specified": 1,
    "Majeed_syndrome|LPIN2-related_disorder": 3,
    "Autoinflammatory_syndrome|Majeed_syndrome": 12,
    "not_specified|not_provided|Majeed_syndrome": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Majeed_syndrome": 2,
    "Autoinflammatory_syndrome|not_provided|Majeed_syndrome": 2,
    "not_provided|Autoinflammatory_syndrome|Majeed_syndrome|not_specified": 1,
    "not_specified|Autoinflammatory_syndrome|not_provided|Majeed_syndrome": 1,
    "not_provided|not_specified|Majeed_syndrome": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Majeed_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Autoinflammatory_syndrome|Majeed_syndrome": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|not_specified|Majeed_syndrome": 1,
    "Majeed_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "LPIN2-related_disorder|Autoinflammatory_syndrome|not_specified|not_provided|Majeed_syndrome": 2,
    "Majeed_syndrome|not_provided|LPIN2-related_disorder": 1,
    "Inborn_genetic_diseases|Majeed_syndrome|Autoinflammatory_syndrome": 1,
    "Majeed_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Majeed_syndrome|not_specified|Autoinflammatory_syndrome": 1,
    "not_provided|Majeed_syndrome|not_specified": 3,
    "not_provided|not_specified|Majeed_syndrome|LPIN2-related_disorder": 1,
    "not_provided|See_cases|Autoinflammatory_syndrome|Majeed_syndrome|LPIN2-related_disorder": 1,
    "Majeed_syndrome|not_provided|not_specified": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Majeed_syndrome|Psoriasis": 1,
    "LPIN2-related_disorder|Majeed_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Majeed_syndrome": 2,
    "Autoinflammatory_syndrome|LPIN2-related_disorder|not_specified|not_provided|Majeed_syndrome": 1,
    "Autoinflammatory_syndrome|Majeed_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Majeed_syndrome|Autoinflammatory_syndrome|LPIN2-related_disorder": 1,
    "not_specified|Majeed_syndrome|Autoinflammatory_syndrome": 2,
    "Majeed_syndrome|not_specified|Autoinflammatory_syndrome|not_provided": 1,
    "LPIN2-related_disorder|not_provided|Majeed_syndrome": 1,
    "MYOM1-related_disorder|not_specified|Hypertrophic_cardiomyopathy": 4,
    "Non-immune_hydrops_fetalis|Hypertrophic_cardiomyopathy": 1,
    "not_specified|MYOM1-related_disorder|Hypertrophic_cardiomyopathy": 5,
    "Hypertrophic_cardiomyopathy|not_specified|MYOM1-related_disorder": 6,
    "Hypertrophic_cardiomyopathy|MYOM1-related_disorder": 5,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|MYOM1-related_disorder": 1,
    "Cardiovascular_phenotype|MYOM1-related_disorder|not_provided|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|MYOM1-related_disorder|not_specified|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|MYOM1-related_disorder|not_specified|not_provided": 2,
    "Hypertrophic_cardiomyopathy|MYOM1-related_non-immune_fetal_hydrops|not_specified": 1,
    "MYOM1-related_disorder": 4,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|MYOM1-related_disorder": 1,
    "MYOM1-related_disorder|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided": 2,
    "MYOM1-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Hypoglycemia|Abnormality_of_the_liver|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Sudden_cardiac_death|not_specified": 1,
    "Hypertrophic_cardiomyopathy|MYOM1-related_disorder|not_provided|not_specified": 2,
    "Hypertrophic_cardiomyopathy|MYOM1-related_disorder|not_specified|not_provided": 3,
    "MYOM1-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 3,
    "not_specified|MYOM1-related_disorder": 1,
    "MYOM1-related_disorder|not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|MYOM1-related_disorder|not_specified": 2,
    "Hypertrophic_cardiomyopathy|not_provided|MYOM1-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|MYOM1-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|MYOM1-related_disorder|not_specified": 2,
    "MYOM1-related_disorder|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "MYOM1-related_non-immune_fetal_hydrops|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|MYOM1-related_disorder": 1,
    "MYOM1-related_disorder|Hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|MYOM1-related_disorder|not_provided|not_specified": 1,
    "MYOM1-related_disorder|not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|MYOM1-related_disorder|not_provided": 1,
    "Holoprosencephaly_4": 57,
    "TGIF1-related_disorder": 8,
    "Holoprosencephaly_4|not_provided": 3,
    "Holoprosencephaly_4|TGIF1-related_disorder": 1,
    "not_provided|Holoprosencephaly_4": 4,
    "TGIF1-related_disorder|not_provided|Holoprosencephaly_4": 1,
    "Holoprosencephaly_4|not_specified": 3,
    "Disorder_of_sexual_differentiation|not_provided": 1,
    "TGIF1-related_disorder|Holoprosencephaly_4|not_provided": 2,
    "not_specified|Holoprosencephaly_4": 1,
    "Holoprosencephaly_sequence|Holoprosencephaly_4|not_provided|not_specified": 1,
    "TGIF1-related_disorder|Holoprosencephaly_4": 1,
    "TGIF1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Holoprosencephaly_4": 1,
    "Inborn_genetic_diseases|Holoprosencephaly_4": 2,
    "Holoprosencephaly_sequence|not_provided|not_specified|Holoprosencephaly_4": 1,
    "not_specified|Holoprosencephaly_sequence|not_provided|Holoprosencephaly_4": 2,
    "Holoprosencephaly_4|Holoprosencephaly_sequence|not_specified|not_provided": 1,
    "Holoprosencephaly_4|TGIF1-related_disorder|not_provided": 1,
    "not_provided|Holoprosencephaly_sequence|Holoprosencephaly_4|not_specified": 1,
    "DLGAP1-related_disorder": 24,
    "not_provided|DLGAP1-related_disorder": 3,
    "DLGAP1-related_disorder|not_provided": 2,
    "ARHGAP28-related_disorder": 1,
    "Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 86,
    "Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|not_provided": 27,
    "not_provided|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 34,
    "LAMA1-related_disorder": 13,
    "LAMA1-related_disorder|not_provided": 19,
    "not_specified|LAMA1-related_disorder|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 3,
    "Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_specified|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|Retinal_dystrophy|not_provided": 1,
    "not_provided|LAMA1-related_disorder": 14,
    "not_provided|Inborn_genetic_diseases|LAMA1-related_disorder": 2,
    "not_provided|LAMA1-related_disorder|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 1,
    "Inborn_genetic_diseases|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 5,
    "Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|Retinal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|LAMA1-related_disorder": 1,
    "Inborn_genetic_diseases|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|not_provided": 2,
    "LAMA1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Optic_atrophy|Retinal_dystrophy|LAMA1-related_disorder|not_provided": 1,
    "not_provided|Muscular_dystrophy|_congenital|_merosin_deficient_or_partially_deficient": 1,
    "LAMA1-related_disorder|not_specified": 1,
    "LAMA1-related_disorder|not_provided|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 1,
    "not_provided|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|LAMA1-related_disorder": 1,
    "not_provided|LAMA1-related_disorder|not_specified|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 1,
    "LAMA1-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 1,
    "LAMA1-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|not_provided|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome": 1,
    "LAMA1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided|LAMA1-related_disorder": 1,
    "Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|Intellectual_disability|LAMA1-related_disorder|not_provided": 1,
    "LAMA1-related_disorder|not_specified|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "See_cases|not_provided|LAMA1-related_disorder": 1,
    "not_provided|Ataxia_-_intellectual_disability_-_oculomotor_apraxia_-_cerebellar_cysts_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|LAMA1-related_disorder|not_provided": 1,
    "PTPRM-related_disorder": 28,
    "PTPRM-related_disorder|not_provided": 3,
    "not_provided|PTPRM-related_disorder": 1,
    "task-specific_movement_disorders|not_specified": 1,
    "RAB12-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_7": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_7": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_7|Mitochondrial_complex_I_deficiency|_nuclear_type_1|not_specified|not_provided|Parkinson_disease|_mitochondrial": 1,
    "not_provided|not_specified|NDUFV2-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_7|not_provided": 3,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_7": 9,
    "NDUFV2-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_7|not_specified|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_7|not_specified|not_provided": 1,
    "NDUFV2-related_disorder": 1,
    "not_provided|NDUFV2-related_disorder|not_specified": 1,
    "ANKRD12-related_disorder": 8,
    "not_provided|Hypotrichosis_1|not_specified": 1,
    "Hypotrichosis_1": 2,
    "APCDD1-related_disorder|not_provided": 1,
    "APCDD1-related_disorder": 2,
    "not_provided|not_specified|Hypotrichosis_1": 1,
    "not_provided|APCDD1-related_disorder": 1,
    "Hypotrichosis_1|not_specified": 1,
    "Gordon_syndrome": 12,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 16,
    "PIEZO2-related_disorder|Congenital_contracture|not_provided": 1,
    "Inborn_genetic_diseases|Gordon_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided|Distal_arthrogryposis": 1,
    "Gordon_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|Gordon_syndrome|Marden-Walker_syndrome": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome": 1,
    "not_provided|PIEZO2-related_disorder": 7,
    "PIEZO2-related_disorder|Inborn_genetic_diseases": 2,
    "Marden-Walker_syndrome": 7,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 51,
    "Inborn_genetic_diseases|Distal_arthrogryposis": 1,
    "PIEZO2-related_disorder|not_provided": 9,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided|PIEZO2-related_disorder|Inborn_genetic_diseases": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_specified|not_provided|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided": 1,
    "PIEZO2-related_disorder": 26,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Inborn_genetic_diseases": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|not_provided": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 1,
    "not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|not_specified|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 3,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Gordon_syndrome": 1,
    "not_specified|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided": 1,
    "Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 2,
    "Congenital_contracture": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Gordon_syndrome|Marden-Walker_syndrome|not_provided": 1,
    "Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|PIEZO2-related_disorder|not_provided|not_specified": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 9,
    "not_provided|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 10,
    "not_provided|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Inborn_genetic_diseases": 2,
    "Cleft_palate|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Marden-Walker_syndrome": 1,
    "not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_specified": 1,
    "not_provided|Gordon_syndrome|Inborn_genetic_diseases": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Inborn_genetic_diseases": 1,
    "not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_specified|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "PIEZO2-related_disorder|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided": 1,
    "PIEZO2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_specified|not_provided": 1,
    "FAM38B-related_disorder|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "not_specified|not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 3,
    "not_provided|Gordon_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome": 1,
    "Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Inborn_genetic_diseases": 1,
    "Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided": 2,
    "not_provided|autosomal_recessive_PIEZO2_associated_disease": 1,
    "not_specified|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided|Gordon_syndrome|Marden-Walker_syndrome": 1,
    "not_specified|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Gordon_syndrome|not_provided|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "not_provided|Gordon_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "PIEZO2-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_specified": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided": 2,
    "not_provided|not_specified|autosomal_recessive_PIEZO2_associated_disease|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "Inborn_genetic_diseases|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "Marden-Walker_syndrome|not_provided": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "PIEZO2-related_disorder|not_specified": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|not_provided|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|not_specified": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|not_provided|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 3,
    "PIEZO2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Gordon_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Gordon_syndrome|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 1,
    "PIEZO2-related_disorder|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Gordon_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 1,
    "not_provided|Cerebral_palsy": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "not_provided|Marden-Walker_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|PIEZO2-related_disorder": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Inborn_genetic_diseases|not_provided": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome|Gordon_syndrome": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "Marden-Walker_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Marden-Walker_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Gordon_syndrome": 1,
    "Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Gordon_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Marden-Walker_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Gordon_syndrome|Arthrogryposis-_oculomotor_limitation-electroretinal_anomalies_syndrome|Arthrogryposis|_distal|_with_impaired_proprioception_and_touch": 1,
    "Congenital_ichthyosiform_erythroderma|Exocrine_pancreatic_insufficiency|Scoliosis|Failure_to_thrive": 1,
    "not_specified|Dystonia_25|not_provided": 1,
    "not_provided|GNAL-related_disorder": 1,
    "Dystonia_25|not_specified": 1,
    "GNAL-related_disorder|not_provided|Dystonic_disorder": 1,
    "Dystonic_disorder|GNAL-related_disorder|not_provided": 2,
    "Dystonia_25": 12,
    "GNAL-related_disorder": 3,
    "not_provided|GNAL-related_disorder|Dystonic_disorder": 1,
    "Dystonic_disorder|GNAL-related_disorder": 2,
    "Limb_dystonia|Dysarthria": 1,
    "Dystonic_disorder|Dystonia_25": 1,
    "Dystonic_disorder|GNAL-related_disorder|Dystonia_25": 1,
    "GNAL-related_disorder|Dystonic_disorder": 1,
    "Dystonia_25|not_specified|not_provided": 1,
    "Dystonia_25|not_provided": 1,
    "Dystonic_disorder|Dystonia_25|not_provided": 1,
    "not_provided|Dystonia_25|Dystonic_disorder": 1,
    "GNAL-related_disorder|Dystonic_disorder|not_provided": 1,
    "not_provided|Facial_palsy|_congenital|_with_ptosis_and_velopharyngeal_dysfunction": 4,
    "Facial_palsy|_congenital|_with_ptosis_and_velopharyngeal_dysfunction": 5,
    "TUBB6-related_disorder|not_provided|Facial_palsy|_congenital|_with_ptosis_and_velopharyngeal_dysfunction": 1,
    "TUBB6-related_disorder": 6,
    "Spinocerebellar_ataxia_type_28": 39,
    "not_provided|Spinocerebellar_ataxia_type_28": 14,
    "Spinocerebellar_ataxia_type_28|not_provided": 13,
    "Spastic_ataxia_5|Optic_atrophy_12|Spinocerebellar_ataxia_type_28|not_provided": 1,
    "AFG3L2-related_disorder|not_specified|not_provided|Spinocerebellar_ataxia_type_28": 1,
    "not_provided|Spastic_ataxia_5": 5,
    "AFG3L2-related_disorder|not_specified|not_provided|Spastic_ataxia_5|Spinocerebellar_ataxia_type_28": 1,
    "not_provided|Optic_atrophy_12|Spinocerebellar_ataxia_type_28|Spastic_ataxia_5": 1,
    "Optic_atrophy_12|Spastic_ataxia_5|Spinocerebellar_ataxia_type_28|not_provided": 1,
    "AFG3L2-related_disorder": 5,
    "Spastic_ataxia_5|Optic_atrophy_12|Spinocerebellar_ataxia_type_28|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_type_28|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Optic_atrophy_12": 1,
    "Spinocerebellar_ataxia_type_28|Optic_atrophy_12|Spastic_ataxia_5|not_provided": 2,
    "Spastic_ataxia_5": 8,
    "not_provided|Spastic_ataxia_5|Spinocerebellar_ataxia_type_28": 1,
    "Optic_atrophy_12|not_specified|not_provided": 1,
    "Spastic_ataxia_5|not_provided": 2,
    "Optic_atrophy_12|Glycogen_storage_disease_type_III|Spastic_ataxia_5": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_28": 2,
    "Spastic_ataxia_5|Optic_atrophy_12|Spinocerebellar_ataxia_type_28": 1,
    "Spinocerebellar_ataxia_type_28|Optic_atrophy_12|not_specified|Spastic_ataxia_5|not_provided": 1,
    "Optic_atrophy_12|Spastic_paraparesis|Optic_atrophy": 1,
    "Spinocerebellar_ataxia_type_28|not_specified": 1,
    "Optic_atrophy_12|Optic_atrophy": 1,
    "Spastic_ataxia_5|Spinocerebellar_ataxia_type_28|not_provided": 2,
    "Intellectual_disability|Optic_atrophy": 1,
    "not_provided|Spinocerebellar_ataxia_type_28|Optic_atrophy_12|Spastic_ataxia_5|not_specified": 1,
    "Optic_atrophy_12|Spinocerebellar_ataxia_type_28|Spastic_ataxia_5|Optic_atrophy|not_provided": 1,
    "not_provided|AFG3L2-related_disorder": 4,
    "Optic_atrophy|Reduced_tendon_reflexes": 1,
    "not_provided|Optic_atrophy_12|Sensorineural_hearing_loss_disorder|Optic_atrophy": 1,
    "AFG3L2-associated_disorder": 1,
    "not_specified|not_provided|Optic_atrophy_12|Optic_atrophy|Hyperkinetic_movements|Abnormal_cerebellum_morphology|Dystonic_disorder": 1,
    "AFG3L2-related_disorder|not_provided|Spinocerebellar_ataxia_type_28|not_specified": 1,
    "not_provided|Spinocerebellar_ataxia_type_28|AFG3L2-related_disorder": 1,
    "Spinocerebellar_ataxia_type_28|Optic_atrophy_12|not_provided|Spastic_ataxia_5": 1,
    "Spastic_ataxia_5|Spinocerebellar_ataxia_type_28|not_provided|Optic_atrophy_12|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_28|not_specified": 1,
    "not_specified|not_provided|AFG3L2-related_disorder|Spinocerebellar_ataxia_type_28": 1,
    "Optic_atrophy_12|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_28": 1,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_28": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|AFG3L2-related_disorder|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_28|not_provided|not_specified": 1,
    "CEP76-related_disorder": 5,
    "not_provided|PSMG2-related_disorder": 1,
    "Proteasome-associated_autoinflammatory_syndrome_4": 2,
    "not_provided|not_specified|PSMG2-related_disorder": 1,
    "Proteasome-associated_autoinflammatory_syndrome_4|not_provided": 1,
    "not_provided|Proteasome-associated_autoinflammatory_syndrome_4": 1,
    "not_specified|Proteasome-associated_autoinflammatory_syndrome_4|not_provided": 1,
    "Glucocorticoid_deficiency_1": 93,
    "Glucocorticoid_deficiency_1|not_provided": 18,
    "Glucocorticoid_Deficiency": 17,
    "Glucocorticoid_Deficiency|not_provided": 11,
    "not_provided|Glucocorticoid_deficiency_1": 4,
    "Glucocorticoid_deficiency_1|MC2R-related_disorder|not_provided": 1,
    "MC2R-related_disorder": 1,
    "Glucocorticoid_deficiency_1|Glucocorticoid_Deficiency": 3,
    "Inborn_genetic_diseases|Glucocorticoid_deficiency_1": 2,
    "Glucocorticoid_Deficiency|Glucocorticoid_deficiency_1": 1,
    "Glucocorticoid_deficiency_1|Inborn_genetic_diseases": 2,
    "not_provided|Glucocorticoid_deficiency_1|Glucocorticoid_Deficiency": 1,
    "Glucocorticoid_Deficiency|not_provided|Glucocorticoid_deficiency_1": 1,
    "Glucocorticoid_deficiency_1|MC2R-related_disorder|not_specified": 1,
    "Glucocorticoid_deficiency_1|Glucocorticoid_Deficiency|MC2R-related_disorder|not_provided": 1,
    "not_provided|Glucocorticoid_Deficiency": 2,
    "GREB1L-related_disorder": 48,
    "Renal_agenesis_and_hypodysplasia|Renal_hypodysplasia/aplasia_3": 1,
    "Renal_hypodysplasia/aplasia_3|Hearing_loss|_autosomal_dominant_80": 2,
    "Renal_hypodysplasia/aplasia_3": 51,
    "not_provided|GREB1L-related_disorder": 13,
    "GREB1L-related_disorder|not_provided": 14,
    "GREB1L-related_disorder|not_provided|Mayer-Rokitansky-Kuster-Hauser_syndrome|Renal_hypodysplasia/aplasia_3": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss|Hearing_loss|_autosomal_dominant_80": 1,
    "Renal_agenesis_and_hypodysplasia": 9,
    "Mayer-Rokitansky-K\u00fcster-Hauser_syndrome_type_2|Renal_hypodysplasia/aplasia_3|not_provided": 1,
    "Hearing_loss|_autosomal_dominant_80": 16,
    "Profound_hearing_impairment|Hearing_loss|_autosomal_dominant_80": 1,
    "Hearing_loss|_autosomal_dominant_80|Inner_ear_malformation": 2,
    "Renal_hypodysplasia/aplasia_3|not_provided": 1,
    "Mayer-Rokitansky-K\u00fcster-Hauser_syndrome_type_2": 7,
    "Renal_agenesis|Anhydramnios": 3,
    "Renal_hypodysplasia/aplasia_3|Mayer-Rokitansky-Kuster-Hauser_syndrome": 3,
    "Mayer-Rokitansky-Kuster-Hauser_syndrome|Renal_hypodysplasia/aplasia_3": 6,
    "GREB1L-related_disorder|not_provided|Renal_hypodysplasia/aplasia_3": 1,
    "not_provided|Renal_hypodysplasia/aplasia_3": 3,
    "GREB1L-related_disorder|Renal_hypodysplasia/aplasia_3|Renal_cortical_hyperechogenicity|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_80|Renal_hypodysplasia/aplasia_3": 1,
    "not_provided|Hearing_loss|_autosomal_dominant_80": 1,
    "not_provided|Mayer_Rokitansky_Kuster_Hauser_syndrome_type_1|Hearing_loss|_autosomal_dominant_80": 1,
    "Renal_hypodysplasia/aplasia_3|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Renal_hypodysplasia/aplasia_3|Hearing_loss|_autosomal_dominant_80|not_provided": 1,
    "Mayer_Rokitansky_Kuster_Hauser_syndrome_type_1|Renal_hypodysplasia/aplasia_3": 1,
    "Renal_agenesis_and_hypodysplasia|not_provided": 1,
    "Left_ventricular_noncompaction_7": 20,
    "MIB1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Left_ventricular_noncompaction_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Left_ventricular_noncompaction_7": 1,
    "MIB1-related_disorder|Inborn_genetic_diseases": 2,
    "MIB1-related_disorder": 10,
    "Inborn_genetic_diseases|MIB1-related_disorder|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_7|not_specified|not_provided": 1,
    "Paroxysmal_atrial_fibrillation": 1,
    "Inborn_genetic_diseases|not_provided|MIB1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Left_ventricular_noncompaction_7": 1,
    "not_specified|not_provided|Left_ventricular_noncompaction_7": 2,
    "not_provided|MIB1-related_disorder": 3,
    "not_provided|Left_ventricular_noncompaction_7": 3,
    "Inborn_genetic_diseases|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Left_ventricular_noncompaction_7|Inborn_genetic_diseases|not_specified|MIB1-related_disorder": 1,
    "not_provided|not_specified|Left_ventricular_noncompaction_7": 2,
    "Left_ventricular_noncompaction_7|not_provided": 2,
    "not_specified|Left_ventricular_noncompaction_7": 1,
    "not_specified|Left_ventricular_noncompaction_7|not_provided": 1,
    "Inborn_genetic_diseases|MIB1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Left_ventricular_noncompaction_7": 1,
    "not_provided|Left_ventricular_noncompaction_7|MIB1-related_disorder": 1,
    "MIB1-related_disorder|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_7|not_provided|Inborn_genetic_diseases": 1,
    "Left_ventricular_noncompaction_7|not_provided|MIB1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Left_ventricular_noncompaction_7": 1,
    "Atrioventricular_septal_defect_5": 397,
    "not_provided|GATA6-related_disorder": 1,
    "not_provided|Atrioventricular_septal_defect_5|Inborn_genetic_diseases": 1,
    "Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Tetralogy_of_Fallot|Conotruncal_heart_malformations": 2,
    "Atrioventricular_septal_defect_5|not_specified|not_provided|Monogenic_diabetes|GATA6-related_disorder": 1,
    "Atrioventricular_septal_defect_5|not_provided": 16,
    "GATA6-related_disorder": 17,
    "Atrioventricular_septal_defect_5|GATA6-related_disorder": 5,
    "Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 15,
    "Atrioventricular_septal_defect_5|not_specified": 2,
    "GATA6-related_disorder|Atrioventricular_septal_defect_5": 4,
    "Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Monogenic_diabetes|Atrioventricular_septal_defect_5": 1,
    "not_provided|Atrioventricular_septal_defect_5": 19,
    "Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Tetralogy_of_Fallot": 2,
    "Inborn_genetic_diseases|Atrioventricular_septal_defect_5": 8,
    "not_provided|not_specified|Atrioventricular_septal_defect_5": 2,
    "Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 1,
    "Atrioventricular_septal_defect_5|not_provided|Conotruncal_heart_malformations|Atrial_septal_defect_9|Tetralogy_of_Fallot|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Atrioventricular_septal_defect_5|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|not_specified": 1,
    "Atrioventricular_septal_defect_5|Inborn_genetic_diseases": 6,
    "Monogenic_diabetes|not_provided|Atrioventricular_septal_defect_5|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 1,
    "Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Atrioventricular_septal_defect_5|not_provided": 1,
    "Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Tetralogy_of_Fallot|Atrioventricular_septal_defect_5|Atrial_septal_defect_9": 1,
    "Atrioventricular_septal_defect_5|not_provided|Monogenic_diabetes": 1,
    "Tetralogy_of_Fallot|not_provided|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 1,
    "Monogenic_diabetes|Tetralogy_of_Fallot|Atrioventricular_septal_defect_5|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Atrioventricular_septal_defect_5": 1,
    "not_provided|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Tetralogy_of_Fallot": 1,
    "Abnormal_cardiovascular_system_morphology|Congenital_diaphragmatic_hernia|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 2,
    "Tetralogy_of_Fallot|Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Atrioventricular_septal_defect_5": 3,
    "not_specified|not_provided|Atrioventricular_septal_defect_5|Neonatal_insulin-dependent_diabetes_mellitus|Monogenic_diabetes": 1,
    "not_provided|GATA6-related_disorder|Atrioventricular_septal_defect_5": 1,
    "not_provided|GATA6-related_disorder|not_specified|Atrioventricular_septal_defect_5": 1,
    "not_provided|Atrioventricular_septal_defect_5|Persistent_truncus_arteriosus": 1,
    "Atrioventricular_septal_defect_5|Inborn_genetic_diseases|not_provided": 1,
    "GATA6-related_disorder|Atrioventricular_septal_defect_5|not_provided|Conotruncal_heart_malformations|Atrial_septal_defect_9|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Tetralogy_of_Fallot": 1,
    "Atrioventricular_septal_defect_5|Atrial_septal_defect_9": 1,
    "Atrioventricular_septal_defect_5|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrial_septal_defect_9": 1,
    "Tetralogy_of_Fallot|Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|Atrial_septal_defect_9": 1,
    "Atrioventricular_septal_defect_5|GATA6-related_disorder|not_provided": 1,
    "GATA6-related_disorder|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Atrioventricular_septal_defect_5": 1,
    "not_specified|Atrioventricular_septal_defect_5": 1,
    "Atrial_septal_defect_9": 2,
    "Neutropenia|_severe_congenital|_8|_autosomal_dominant|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 1,
    "Congenital_diaphragmatic_hernia|Abnormal_cardiovascular_system_morphology|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome": 2,
    "Inborn_genetic_diseases|Conotruncal_heart_malformations|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|Tetralogy_of_Fallot|not_specified|not_provided": 1,
    "not_specified|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|not_provided|Monogenic_diabetes|GATA6-related_disorder|Atrioventricular_septal_defect_5": 1,
    "GATA6-related_congenital_heart_disease_with_or_without_pancreatic_agenesis_or_neonatal_diabetes": 1,
    "Persistent_truncus_arteriosus": 1,
    "Atrioventricular_septal_defect_5|Persistent_truncus_arteriosus": 1,
    "Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5": 1,
    "Atypical_coarctation_of_aorta": 3,
    "not_specified|not_provided|Atrioventricular_septal_defect_5": 1,
    "not_specified|not_provided|Atrioventricular_septal_defect_5|Neonatal_insulin-dependent_diabetes_mellitus": 1,
    "Atrioventricular_septal_defect_5|not_specified|not_provided": 1,
    "Atrioventricular_septal_defect_5|not_provided|Inborn_genetic_diseases": 1,
    "Conotruncal_heart_malformations|Tetralogy_of_Fallot|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Atrioventricular_septal_defect_5|Atrial_septal_defect_9|not_provided|Inborn_genetic_diseases": 1,
    "Monogenic_diabetes|Atrioventricular_septal_defect_5|not_provided|Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|GATA6-related_disorder": 1,
    "Pancreatic_hypoplasia-diabetes-congenital_heart_disease_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Atrioventricular_septal_defect_5|Atrial_septal_defect_9": 1,
    "RBBP8-related_disorder|not_specified|not_provided": 3,
    "not_provided|Seckel_syndrome_2": 2,
    "not_provided|not_specified|RBBP8-related_disorder": 1,
    "not_specified|RBBP8-related_disorder|not_provided": 1,
    "RBBP8-related_disorder|not_provided": 5,
    "Jawad_syndrome|Seckel_syndrome_2|Inborn_genetic_diseases|not_provided": 1,
    "Jawad_syndrome|Seckel_syndrome_2|not_specified": 1,
    "Jawad_syndrome": 4,
    "Seckel_syndrome_2": 2,
    "Jawad_syndrome|Seckel_syndrome_2|not_provided": 3,
    "RBBP8-related_disorder": 3,
    "not_provided|Jawad_syndrome|Seckel_syndrome_2": 2,
    "Seckel_syndrome_2|Jawad_syndrome|not_provided": 1,
    "Seckel_syndrome|Jawad_syndrome|not_provided": 1,
    "RBBP8-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|Seckel_syndrome_2|Jawad_syndrome": 1,
    "Seckel_syndrome_2|Jawad_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Jawad_syndrome|not_provided": 1,
    "not_provided|RBBP8-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Seckel_syndrome_2|Jawad_syndrome": 1,
    "Jawad_syndrome|Seckel_syndrome_2": 1,
    "not_specified|Seckel_syndrome_2|not_provided|Jawad_syndrome": 1,
    "not_provided|Jawad_syndrome|not_specified|Seckel_syndrome_2": 1,
    "Seckel_syndrome_2|Jawad_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Jawad_syndrome": 1,
    "Hereditary_cancer|not_specified": 1,
    "Niemann-Pick_disease|_type_C|not_provided": 1,
    "Niemann-Pick_disease|_type_C1|not_provided": 84,
    "NPC1-related_disorder|not_provided|Niemann-Pick_disease|_type_C1": 7,
    "Niemann-Pick_disease|_type_C1|not_specified": 23,
    "not_provided|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 4,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 38,
    "NPC1-related_disorder|Niemann-Pick_disease|_type_C1": 26,
    "not_provided|not_specified|Niemann-Pick_disease|_type_C1": 5,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|not_provided": 8,
    "Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C1": 3,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder|not_provided": 6,
    "Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C|NPC1-related_disorder": 3,
    "Niemann-Pick_disease|_type_C1|not_specified|not_provided": 7,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1": 24,
    "Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C|not_provided": 5,
    "not_provided|NPC1-related_disorder|Niemann-Pick_disease|_type_C1": 2,
    "Niemann-Pick_disease|_type_C1|not_provided|Inborn_genetic_diseases": 3,
    "Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C": 14,
    "Inborn_genetic_diseases|NPC1-related_disorder|not_provided|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 22,
    "Niemann-Pick_disease|_type_C1|_juvenile_form": 1,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|not_provided": 6,
    "Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 1,
    "not_provided|Russell-Silver_syndrome|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 2,
    "Niemann-Pick_disease|_type_C|not_provided|Niemann-Pick_disease|_type_C1|Abnormality_of_metabolism/homeostasis": 1,
    "not_specified|Niemann-Pick_disease|_type_C1|not_provided": 5,
    "NPC1-related_disorder": 15,
    "Niemann-Pick_disease|_type_C1|not_provided|Niemann-Pick_disease|_type_C": 5,
    "not_specified|Niemann-Pick_disease|_type_C1": 20,
    "Inborn_genetic_diseases|NPC1-related_disorder|not_specified|not_provided|Niemann-Pick_disease|_type_C1": 4,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|not_specified": 1,
    "Niemann-Pick_disease|_type_C1|not_specified|NPC1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Niemann-Pick_disease|_type_C1|not_specified|Dystonic_disorder": 1,
    "Niemann-Pick_disease|_type_C|not_provided|Niemann-Pick_disease|_type_C1": 8,
    "Inborn_genetic_diseases|not_specified|Niemann-Pick_disease|_type_C1|not_provided": 1,
    "not_specified|not_provided|Niemann-Pick_disease|_type_C1": 11,
    "NPC1-related_disorder|Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C1": 3,
    "Niemann-Pick_disease|_type_C1|not_provided|NPC1-related_disorder": 3,
    "Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases|not_provided": 5,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|NPC1-related_disorder|not_provided": 1,
    "NPC1-related_disorder|not_specified|not_provided|Niemann-Pick_disease|_type_C1": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Niemann-Pick_disease|_type_C1": 2,
    "Inborn_genetic_diseases|not_specified|Niemann-Pick_disease|_type_C1": 2,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder|not_specified": 2,
    "Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C1|_juvenile_form": 1,
    "not_provided|NPC1-related_disorder|not_specified|Niemann-Pick_disease|_type_C1": 1,
    "not_provided|NPC1-related_disorder|Niemann-Pick_disease|_type_C1|not_specified": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|not_provided|NPC1-related_disorder|Russell-Silver_syndrome": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_C1": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases": 4,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Niemann-Pick_disease|_type_C|Sphingomyelin/cholesterol_lipidosis|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C1|_adult_form|Niemann-Pick_disease|_type_C1": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|Cognitive_impairment|Speech_apraxia|Cataplexy|Cerebellar_ataxia|Postural_instability|Headache": 1,
    "not_provided|NPC1-related_disorder|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_D|Niemann-Pick_disease|_type_C1|not_provided|Niemann-Pick_disease|_type_C": 1,
    "not_provided|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 6,
    "NPC1-related_disorder|not_provided|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 2,
    "Niemann-Pick_disease|_type_C1|Intellectual_disability": 1,
    "NPC1-related_disorder|Niemann-Pick_disease|_type_C1|not_provided": 8,
    "not_provided|Niemann-Pick_disease|_type_C1|not_specified": 6,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|not_provided|Niemann-Pick_disease|_type_C1|_juvenile_form": 1,
    "Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases": 14,
    "not_provided|Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C": 2,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C|not_provided": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C|NPC1-related_disorder|Niemann-Pick_disease|_type_C1|not_provided": 1,
    "not_provided|See_cases|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C1|_adult_form": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C1|See_cases": 1,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder|not_specified|not_provided": 2,
    "not_provided|Intellectual_disability|Niemann-Pick_disease|_type_C1": 1,
    "Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases|NPC1-related_disorder": 1,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|NPC1-related_disorder": 1,
    "not_specified|Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 1,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|Sphingomyelin/cholesterol_lipidosis": 2,
    "NPC1-related_disorder|not_provided|Niemann-Pick_disease|_type_C1|not_specified": 1,
    "not_specified|not_provided|NPC1-related_disorder|Niemann-Pick_disease|_type_C1": 1,
    "NPC1-related_disorder|Niemann-Pick_disease|_type_C1|not_provided|not_specified": 2,
    "NPC1-related_disorder|Niemann-Pick_disease|_type_C1|not_specified|not_provided": 1,
    "Niemann-Pick_disease|_type_C1|not_specified|Niemann-Pick_disease|_type_C|not_provided": 1,
    "Niemann-Pick_disease|_type_C1|NPC1-related_disorder|Niemann-Pick_disease|_type_C": 1,
    "not_specified|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 1,
    "Niemann-Pick_disease|_type_C1|not_provided|Niemann-Pick_disease|_type_C|NPC1-related_disorder": 1,
    "Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1": 1,
    "NPC1-related_disorder|not_specified|Niemann-Pick_disease|_type_C1": 1,
    "NPC1-related_disorder|not_provided|Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases": 1,
    "NPC1-related_disorder|not_provided": 1,
    "Niemann-Pick_disease|_type_C1|Cerebellar_ataxia|Cataplexy|Cognitive_impairment|Postural_instability|Speech_apraxia|Headache|not_provided": 1,
    "Capillary_hemangioma": 1,
    "Niemann-Pick_disease|_type_C1|not_specified|NPC1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 1,
    "Niemann-Pick_disease|_type_C1|not_provided|NPC1-related_disorder|Inborn_genetic_diseases": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases|not_specified|Niemann-Pick_disease|_type_C1|not_provided": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1": 1,
    "not_specified|not_provided|Nasopharyngeal_carcinoma|Niemann-Pick_disease|_type_C1": 1,
    "NPC1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Niemann-Pick_disease|_type_C1": 1,
    "not_provided|not_specified|Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 1,
    "NPC1-related_disorder|Niemann-Pick_disease|_type_C1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Niemann-Pick_disease|_type_C1|Niemann-Pick_disease|_type_C|Niemann-Pick_disease|_type_C1|_juvenile_form": 1,
    "not_provided|not_specified|Niemann-Pick_disease|_type_C1|NPC1-related_disorder": 1,
    "Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases|not_specified": 1,
    "NPC1-related_disorder|Niemann-Pick_disease|_type_C1|Inborn_genetic_diseases|not_provided": 1,
    "Niemann-Pick_disease|_type_C|Sphingomyelin/cholesterol_lipidosis": 1,
    "not_provided|Inborn_genetic_diseases|Niemann-Pick_disease|_type_C1|not_specified": 1,
    "not_provided|Niemann-Pick_disease|_type_C": 1,
    "Inborn_genetic_diseases|LAMA3-related_disorder": 3,
    "LAMA3-related_disorder|not_provided": 13,
    "not_provided|LAMA3-related_disorder": 11,
    "LAMA3-related_disorder": 13,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 4,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 7,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Laryngo-onycho-cutaneous_syndrome": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Laryngo-onycho-cutaneous_syndrome": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Laryngo-onycho-cutaneous_syndrome": 1,
    "Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases|not_provided": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 2,
    "Epidermolysis_bullosa|_junctional_2A|_intermediate": 2,
    "LAMA3-related_disorder|Epidermolysis_bullosa|_junctional_2A|_intermediate": 1,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Inborn_genetic_diseases|not_provided|LAMA3-related_disorder": 4,
    "Epidermolysis_bullosa|_junctional_2B|_severe": 7,
    "Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Epidermolysis_bullosa|_junctional_2B|_severe|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2A|_intermediate": 2,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified": 1,
    "Inborn_genetic_diseases|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided": 1,
    "not_specified|not_provided|LAMA3-related_disorder": 1,
    "not_provided|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "not_provided|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_specified": 1,
    "Laryngo-onycho-cutaneous_syndrome": 4,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 2,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Laryngo-onycho-cutaneous_syndrome": 1,
    "Laryngo-onycho-cutaneous_syndrome|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|LAMA3-related_disorder": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|not_provided": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_provided": 10,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome": 17,
    "Inborn_genetic_diseases|not_provided|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Laryngo-onycho-cutaneous_syndrome|not_specified": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 23,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 14,
    "Laryngo-onycho-cutaneous_syndrome|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa": 1,
    "not_provided|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases": 1,
    "LAMA3-related_disorder|not_provided|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Laryngo-onycho-cutaneous_syndrome": 4,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Laryngo-onycho-cutaneous_syndrome": 1,
    "Laryngo-onycho-cutaneous_syndrome|Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|not_provided|Inborn_genetic_diseases": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|not_provided": 1,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate": 16,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 7,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified|not_provided": 2,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate|Laryngo-onycho-cutaneous_syndrome": 1,
    "LAMA3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|LAMA3-related_disorder|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases|Laryngo-onycho-cutaneous_syndrome": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome": 1,
    "Laryngo-onycho-cutaneous_syndrome|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 2,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|LAMA3-related_disorder": 1,
    "Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Laryngo-onycho-cutaneous_syndrome|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Inborn_genetic_diseases|LAMA3-related_disorder|not_provided": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_provided": 1,
    "LAMA3-related_disorder|Inborn_genetic_diseases|not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome": 1,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Epidermolysis_bullosa|_junctional_2B|_severe|not_provided": 1,
    "LAMA3-related_disorder|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_provided": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_specified|not_provided": 1,
    "not_provided|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome": 3,
    "Laryngo-onycho-cutaneous_syndrome|LAMA3-related_disorder|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Inborn_genetic_diseases": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Laryngo-onycho-cutaneous_syndrome|LAMA3-related_disorder|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Inborn_genetic_diseases|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 3,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|not_provided|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|not_provided": 2,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa|not_provided": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|LAMA3-related_disorder|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_2B|_severe|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Laryngo-onycho-cutaneous_syndrome": 1,
    "Epidermolysis_bullosa|_junctional_2B|_severe|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|not_provided": 1,
    "Epidermolysis_bullosa|_junctional_2B|_severe|LAMA3-related_disorder|not_provided": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|not_specified": 3,
    "not_provided|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|LAMA3-related_disorder|not_provided": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|LAMA3-related_disorder|not_specified|not_provided": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2B|_severe|Epidermolysis_bullosa|_junctional_2A|_intermediate": 1,
    "Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|LAMA3-related_disorder": 2,
    "Laryngo-onycho-cutaneous_syndrome|not_provided|not_specified|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "not_provided|LAMA3-related_disorder|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Junctional_epidermolysis_bullosa|_non-Herlitz_type": 1,
    "Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|Epidermolysis_bullosa|_junctional_2A|_intermediate|Epidermolysis_bullosa|_junctional_2B|_severe|not_provided": 1,
    "Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_provided|Laryngo-onycho-cutaneous_syndrome": 1,
    "not_provided|Laryngo-onycho-cutaneous_syndrome|Junctional_epidermolysis_bullosa|_non-Herlitz_type|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|not_specified": 1,
    "Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome|not_provided|not_specified": 1,
    "Laryngo-onycho-cutaneous_syndrome|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz": 1,
    "LAMA3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Junctional_epidermolysis_bullosa_gravis_of_Herlitz|Laryngo-onycho-cutaneous_syndrome": 1,
    "not_provided|TAF4B-related_disorder": 3,
    "TAF4B-related_disorder": 6,
    "Spermatogenic_failure_13": 1,
    "not_specified|Scalp-ear-nipple_syndrome": 2,
    "Scalp-ear-nipple_syndrome": 32,
    "not_provided|Scalp-ear-nipple_syndrome|not_specified": 1,
    "KCTD1-related_disorder|not_provided": 1,
    "Scalp-ear-nipple_syndrome|not_specified": 3,
    "not_provided|not_specified|Scalp-ear-nipple_syndrome": 1,
    "Scalp-ear-nipple_syndrome|not_provided": 1,
    "Scalp-ear-nipple_syndrome|not_provided|KCTD1-related_disorder": 1,
    "KCTD1-related_disorder": 6,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_4|_remitting": 2,
    "AQP4-related_disorder": 3,
    "CDH2-related_disorder": 8,
    "Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome|Syndromic_neurodevelopmental_disorder|Axon_pathfinding|_cardiac|_ocular_and_genital_defects|Corpus_callosum|_agenesis_of": 3,
    "not_provided|Inborn_genetic_diseases|Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "CDH2-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome|Syndromic_neurodevelopmental_disorder|CDH2-related_disorder|Axon_pathfinding|_cardiac|_ocular_and_genital_defects|Corpus_callosum|_agenesis_of|not_provided": 1,
    "not_provided|CDH2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|CDH2-related_disorder": 1,
    "Syndromic_neurodevelopmental_disorder|Axon_pathfinding|_cardiac|_ocular_and_genital_defects|Corpus_callosum|_agenesis_of": 1,
    "not_provided|Axon_pathfinding|_cardiac|_ocular_and_genital_defects|Corpus_callosum|_agenesis_of": 1,
    "Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome": 3,
    "Axon_pathfinding|_cardiac|_ocular_and_genital_defects|Corpus_callosum|_agenesis_of": 1,
    "Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome|Axon_pathfinding|_cardiac|_ocular_and_genital_defects|Corpus_callosum|_agenesis_of": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|Inborn_genetic_diseases": 1,
    "CDH2-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|Auditory_neuropathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome": 1,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia|_familial|_14": 1,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|not_provided": 1,
    "Inborn_genetic_diseases|CDH2-related_disorder|not_provided": 2,
    "Corpus_callosum|_agenesis_of|Syndromic_neurodevelopmental_disorder|Axon_pathfinding|_cardiac|_ocular_and_genital_defects": 1,
    "not_provided|CDH2-related_disorder": 3,
    "not_provided|Attention_deficit-hyperactivity_disorder_8": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome|CDH2-related_disorder|Inborn_genetic_diseases": 1,
    "CDH2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "CDH2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome|not_provided": 1,
    "not_provided|Agenesis_of_corpus_callosum|_cardiac|_ocular|_and_genital_syndrome": 1,
    "CDH2-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "CDH2-related_disorder|Inborn_genetic_diseases": 1,
    "CDH2-related_disorder|not_provided|not_specified": 3,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Inborn_genetic_diseases": 1,
    "not_specified|CDH2-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|CDH2-related_disorder": 1,
    "Inborn_genetic_diseases|Arrhythmogenic_right_ventricular_dysplasia|_familial|_14|not_provided": 1,
    "not_provided|DSC3-related_disorder": 2,
    "not_provided|Hereditary_hypotrichosis_with_recurrent_skin_vesicles": 1,
    "DSC3-related_disorder": 4,
    "Hereditary_hypotrichosis_with_recurrent_skin_vesicles": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_11": 527,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 12,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 18,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiomyopathy": 2,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 35,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 24,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 5,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 12,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 27,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiomyopathy|DSC2-related_disorder|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 9,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 31,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 42,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 10,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiomyopathy": 1,
    "DSC2-related_disorder|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 8,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype": 7,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 23,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 10,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 2,
    "not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 2,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 7,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|DSC2-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 8,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 3,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype": 3,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 3,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 6,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 4,
    "Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 16,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 7,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiomyopathy": 1,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 1,
    "DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 4,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11": 11,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 7,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 6,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 4,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiovascular_phenotype": 1,
    "DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided": 1,
    "not_provided|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|not_provided": 2,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Cardiomyopathy": 4,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 3,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 6,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 7,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "DSC2-related_disorder|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|See_cases|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiovascular_phenotype": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|DSC2-related_disorder": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 3,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Dilated_cardiomyopathy_1A": 1,
    "not_specified|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 3,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 3,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 2,
    "Primary_dilated_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "not_specified|Cardiomyopathy|not_provided|DSC2-related_disorder|Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiomyopathy|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|DSC2-related_disorder|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia|_familial|_11|_with_mild_palmoplantar_keratoderma_and_woolly_hair": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 3,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 8,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 2,
    "DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype": 4,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 4,
    "Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype": 5,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy": 4,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "ARRHYTHMOGENIC_RIGHT_VENTRICULAR_DYSPLASIA|_FAMILIAL|_11|_WITH_OR_WITHOUT_MILD_PALMOPLANTAR_KERATODERMA|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|not_provided": 1,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 4,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 5,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "DSC2-related_disorder": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 4,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 1,
    "DSC2-related_disorder|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 6,
    "Dilated_cardiomyopathy_1S|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Dilated_cardiomyopathy_1A|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 3,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiac_arrest|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|DSC2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|DSC2-related_disorder": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_1|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 2,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiomyopathy|not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Long_QT_syndrome|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_specified": 1,
    "DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 2,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|DSC2-related_disorder": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|DSC2-related_disorder|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|DSC2-related_disorder|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 1,
    "not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|DSC2-related_disorder|Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy": 1,
    "not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiomyopathy": 1,
    "not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Sudden_unexplained_death|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|DSC2-related_disorder|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_specified|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "DSC2-related_disorder|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|Cardiomyopathy": 1,
    "DSC2-related_disorder|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Primary_familial_dilated_cardiomyopathy|Cardiovascular_phenotype|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|not_specified": 1,
    "DSC2-related_disorder|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_11|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia": 1,
    "Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|Cardiomyopathy|Cardiovascular_phenotype|DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided|Familial_isolated_arrhythmogenic_right_ventricular_dysplasia|not_specified|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_11|not_provided": 1,
    "not_provided|DSC2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_11": 1,
    "DSG1-related_disorder": 3,
    "not_specified|not_provided|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 1,
    "Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|not_provided": 2,
    "Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome": 2,
    "Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome": 4,
    "not_provided|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 2,
    "Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 9,
    "Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse|not_provided": 2,
    "Epidermal_disease|not_provided|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 1,
    "Hereditary_palmoplantar_keratoderma|Bicuspid_aortic_valve": 1,
    "Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|not_provided": 3,
    "Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse|not_provided|not_specified": 1,
    "Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 1,
    "DSG1-related_disorder|not_provided": 12,
    "not_provided|DSG1-related_disorder": 19,
    "Hereditary_palmoplantar_keratoderma|Diffuse_palmoplantar_hyperkeratosis": 1,
    "not_provided|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome": 1,
    "Inborn_genetic_diseases|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|not_provided": 1,
    "DSG1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|not_provided|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 1,
    "Inborn_genetic_diseases|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|not_provided": 1,
    "DSG1-related_disorder|not_specified|not_provided": 1,
    "Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 1,
    "not_provided|Inborn_genetic_diseases|Severe_dermatitis-multiple_allergies-metabolic_wasting_syndrome|Palmoplantar_keratoderma_i|_striate|_focal|_or_diffuse": 1,
    "Hypotrichosis_6": 52,
    "Hypotrichosis_6|DSG4-related_disorder": 1,
    "Hypotrichosis_6|DSG4-related_disorder|not_provided": 8,
    "Hypotrichosis_6|not_provided": 20,
    "Inborn_genetic_diseases|Hypotrichosis_6": 6,
    "DSG4-related_disorder": 8,
    "Hypotrichosis_6|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypotrichosis_6": 13,
    "Hypotrichosis_6|Inborn_genetic_diseases": 5,
    "DSG4-related_disorder|not_provided|Hypotrichosis_6": 1,
    "DSG4-related_disorder|Hypotrichosis_6": 1,
    "not_specified|not_provided|Hypotrichosis_6": 1,
    "Hypotrichosis_6|not_provided|DSG4-related_disorder": 1,
    "not_provided|DSG4-related_disorder": 2,
    "DSG4-related_disorder|not_provided|Hypotrichosis_6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Hypotrichosis_6": 1,
    "DSG4-related_disorder|not_provided": 1,
    "not_provided|Hypotrichosis_6|Inborn_genetic_diseases": 1,
    "Hypotrichosis_6|Inborn_genetic_diseases|DSG4-related_disorder|not_provided": 1,
    "Blistering|_acantholytic|_of_oral_and_laryngeal_mucosa": 2,
    "Dilated_Cardiomyopathy|_Dominant|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 13,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 18,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 19,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 8,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 39,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiomyopathy": 2,
    "DSG2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 31,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 56,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 27,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|Dilated_Cardiomyopathy|_Dominant|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 28,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 3,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 2,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1BB": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 9,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 8,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|not_specified": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10": 8,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 13,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 5,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 4,
    "Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 33,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 6,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "not_provided|not_specified|DSG2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 10,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 2,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 3,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_dysplasia_9": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 3,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|DSG2-related_disorder|not_specified|not_provided|Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Catecholaminergic_polymorphic_ventricular_tachycardia_1|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 6,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|DSG2-related_disorder|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 3,
    "not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "DSG2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 10,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 3,
    "Cardiovascular_phenotype|Cardiac_arrest|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_1": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_9|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|not_specified|Cardiomyopathy": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 8,
    "Cardiomyopathy|not_provided|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 6,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy": 4,
    "Dilated_Cardiomyopathy|_Dominant|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 7,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 3,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 3,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1BB|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|not_provided": 2,
    "Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 3,
    "Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 4,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 3,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 4,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|not_specified": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 4,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiac_arrest|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 9,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 2,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 6,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "DSG2-related_disorder|Dilated_Cardiomyopathy|_Dominant|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|Cardiomyopathy": 1,
    "Intellectual_disability|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Familial_isolated_dilated_cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1BB|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 5,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 3,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 3,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Systolic_heart_failure|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "DSG2-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "not_specified|DSG2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified|DSG2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Dilated_cardiomyopathy_1BB|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|DSG2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1BB|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|DSG2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "DSG2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_1BB": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy": 2,
    "Cardiomyopathy|DSG2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_Cardiomyopathy|_Dominant": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiac_arrest|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_specified": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype": 1,
    "DSG2-related_disorder|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|not_provided": 1,
    "not_specified|not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|DSG2-related_disorder": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_Cardiomyopathy|_Dominant": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|DSG2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 2,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|DSG2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype": 2,
    "Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Hypertrophic_cardiomyopathy": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Primary_familial_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Conduction_disorder_of_the_heart|Arrhythmogenic_right_ventricular_dysplasia_10|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiomyopathy|Restrictive_cardiomyopathy|Dilated_cardiomyopathy_1BB|not_specified": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Long_QT_syndrome|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiomyopathy|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Restrictive_cardiomyopathy|not_specified": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Dilated_cardiomyopathy_1BB|Cardiovascular_phenotype": 1,
    "not_provided|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiomyopathy|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "not_specified|Arrhythmogenic_right_ventricular_dysplasia_10|DSG2-related_disorder|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1BB|Cardiomyopathy": 1,
    "not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "not_provided|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "DSG2-related_disorder|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy": 1,
    "DSG2-related_disorder": 2,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|Cardiomyopathy|not_provided": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|not_specified|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiac_arrhythmia|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|not_provided": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Dilated_cardiomyopathy_1BB|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB|not_specified|not_provided|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Cardiomyopathy|Arrhythmogenic_right_ventricular_dysplasia_10|not_provided": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Dilated_cardiomyopathy_1BB": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|Dilated_cardiomyopathy_1BB": 1,
    "Arrhythmogenic_right_ventricular_dysplasia_10|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "DSG2-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_1BB|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_dysplasia_10|not_specified": 1,
    "Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic": 3,
    "Amyloidosis|_hereditary_systemic_1|not_provided": 10,
    "Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|not_provided": 1,
    "Amyloidosis|_hereditary_systemic_1": 159,
    "Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Cardiovascular_phenotype|not_provided": 1,
    "Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 4,
    "Charcot-Marie-Tooth_disease|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_1": 10,
    "Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic": 2,
    "TTR-related_disorder|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Charcot-Marie-Tooth_disease|not_specified|not_provided|Cardiomyopathy": 1,
    "Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_provided": 4,
    "Amyloidosis|_hereditary_systemic_1|not_provided|Cardiovascular_phenotype": 6,
    "Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 16,
    "Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1": 2,
    "Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_provided": 1,
    "Amyloidosis|_hereditary_systemic_1|not_specified": 3,
    "Cardiomyopathy|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1": 22,
    "Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1": 1,
    "TTR-related_disorder|Amyloidosis|_hereditary_systemic_1": 2,
    "not_specified|Amyloidosis|_hereditary_systemic_1": 3,
    "Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Amyloidosis|_hereditary_systemic_1|not_specified|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Amyloidosis|_hereditary_systemic_1": 1,
    "Amyloidosis|_hereditary_systemic_1|not_specified|not_provided|TTR-related_disorder": 1,
    "Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Charcot-Marie-Tooth_disease|not_specified|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1": 2,
    "Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Charcot-Marie-Tooth_disease|not_specified|not_provided|TRANSTHYRETIN_POLYMORPHISM|Hypertrophic_cardiomyopathy": 1,
    "Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_specified|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1": 1,
    "Amyloidosis|_hereditary_systemic_1|not_provided|Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Amyloidosis|_hereditary_systemic_1": 13,
    "not_specified|Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic": 1,
    "Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|Amyloidosis": 1,
    "Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Cardiovascular_phenotype|not_provided": 1,
    "Carpal_tunnel_syndrome|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_provided": 1,
    "Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1": 5,
    "Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|not_provided": 1,
    "Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_specified": 2,
    "TTR-related_disorder|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_provided|Cardiomyopathy": 1,
    "Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1": 1,
    "not_specified|Cardiomyopathy|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Amyloidosis|_hereditary_systemic_1": 1,
    "not_specified|Tip-toe_gait|not_provided|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|not_provided": 3,
    "Amyloidosis|_hereditary_systemic_1|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Amyloidosis|_hereditary_systemic_1|not_specified": 1,
    "Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic": 1,
    "Amyloidosis|Amyloidosis|_hereditary_systemic_1": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|Cardiomyopathy|not_provided|Amyloidosis|_hereditary_systemic_1": 1,
    "Cardiovascular_phenotype|Carpal_tunnel_syndrome|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Amyloidosis|_hereditary_systemic_1": 1,
    "Cardiovascular_phenotype|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|not_provided": 1,
    "Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_provided": 1,
    "Amyloidosis|_hereditary_systemic_1|Hereditary_amyloidosis": 1,
    "Charcot-Marie-Tooth_disease|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|Cardiovascular_phenotype|not_specified": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|not_provided|Amyloidosis|_hereditary_systemic_1": 1,
    "Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1": 1,
    "not_specified|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|not_provided|Cardiomyopathy|Amyloidosis|_hereditary_systemic_1|Heart_failure": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|TTR-related_disorder|Charcot-Marie-Tooth_disease|Amyloidosis|_hereditary_systemic_1|not_provided": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|not_provided|Cardiomyopathy|Amyloidosis|_hereditary_systemic_1": 1,
    "Amyloidosis|_hereditary_systemic_1|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_specified": 1,
    "TTR-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Amyloidosis|_hereditary_systemic_1": 1,
    "not_provided|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Cardiomyopathy|TTR-related_disorder|Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1": 1,
    "not_specified|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Amyloidosis|_hereditary_systemic_1": 1,
    "Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "TTR-related_disorder|not_specified": 1,
    "Amyloidosis|_hereditary_systemic_1|Cardiomyopathy|Brugada_syndrome|Carpal_tunnel_syndrome_1|Hyperthyroxinemia|_dystransthyretinemic|Cardiovascular_phenotype|not_provided|Conduction_disorder_of_the_heart|not_specified|Charcot-Marie-Tooth_disease": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|Amyloidosis|_hereditary_systemic_1|Cardiomyopathy|not_provided": 1,
    "Amyloidosis|_hereditary_systemic_1|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Amyloidosis|_hereditary_systemic_1|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Hyperthyroxinemia|_dystransthyretinemic|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype|Hereditary_amyloidosis|not_provided": 1,
    "Charcot-Marie-Tooth_disease|TTR-related_disorder|Amyloidosis|_hereditary_systemic_1|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|not_provided|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Amyloidosis|_hereditary_systemic_1|Cardiomyopathy": 1,
    "Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|not_provided": 1,
    "Carpal_tunnel_syndrome_1": 1,
    "Amyloidosis|_hereditary_systemic_1|Cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Amyloidosis|_hereditary_systemic_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|not_specified|not_provided|Cardiomyopathy|Hyperthyroxinemia|_dystransthyretinemic|AMYLOIDOSIS|_HEREDITARY_SYSTEMIC_1|_MODIFIER_OF|Amyloidosis|_hereditary_systemic_1": 1,
    "not_specified|Amyloidosis|_hereditary_systemic_1|not_provided|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Amyloidosis|_hereditary_systemic_1": 1,
    "Cardiovascular_phenotype|ATTRV122I_amyloidosis|TTR-related_disorder|Carpal_tunnel_syndrome_1|Amyloidosis|_hereditary_systemic_1|Hyperthyroxinemia|_dystransthyretinemic|Charcot-Marie-Tooth_disease|not_provided|Cardiomyopathy|Tip-toe_gait|Amyloidosis": 1,
    "Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|Cardiomyopathy": 1,
    "Amyloidosis|_hereditary_systemic_1|not_specified|not_provided": 1,
    "Hyperthyroxinemia|_dystransthyretinemic|Amyloidosis|_hereditary_systemic_1|Carpal_tunnel_syndrome_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Tenorio_syndrome": 30,
    "not_provided|Tenorio_syndrome": 4,
    "Tenorio_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Tenorio_syndrome|not_provided": 1,
    "Tenorio_syndrome|RNF125-related_disorder": 1,
    "Tenorio_syndrome|not_provided": 5,
    "Inborn_genetic_diseases|not_specified|RNF125-related_disorder": 1,
    "Inborn_genetic_diseases|Tenorio_syndrome": 1,
    "RNF125-related_disorder": 3,
    "not_provided|RNF125-related_disorder|Tenorio_syndrome": 1,
    "RNF125-related_disorder|not_provided|Tenorio_syndrome": 1,
    "Tenorio_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "RNF125-related_disorder|Tenorio_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Tenorio_syndrome": 1,
    "not_specified|Tenorio_syndrome": 1,
    "not_specified|RNF125-related_disorder": 1,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 168,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided": 37,
    "ASXL3-related_disorder": 27,
    "not_provided|not_specified|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|ASXL3-related_disorder": 1,
    "not_provided|not_specified|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 3,
    "ASXL3-related_disorder|not_provided": 5,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Inborn_genetic_diseases": 7,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided|ASXL3-related_disorder": 2,
    "not_provided|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 12,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|ASXL3-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 8,
    "Ventricular_septal_defect|Strabismus|Global_developmental_delay": 1,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Intellectual_disability|not_provided": 2,
    "not_provided|not_specified|ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 1,
    "ASXL3-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|ASXL3-related_disorder": 1,
    "ASXL3-related_disorder|Intellectual_disability|not_provided": 1,
    "ASXL3-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided": 1,
    "Language_retardation|intellectual_deficiency|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 1,
    "not_provided|ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 1,
    "not_provided|ASXL3-related_disorder": 4,
    "not_specified|not_provided|ASXL3-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_ataxia|Inborn_genetic_diseases|not_provided": 1,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_specified|not_provided": 2,
    "ASXL3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ASXL3-related_disorder|not_provided|not_specified": 1,
    "not_provided|ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_specified": 2,
    "ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided|not_specified": 1,
    "ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ASXL3-related_disorder|not_provided": 2,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Abnormal_brain_morphology": 1,
    "not_specified|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Intellectual_disability": 1,
    "ASXL3-related_disorder|Intellectual_disability": 1,
    "ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided": 2,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Intellectual_disability": 1,
    "Rare_syndromic_intellectual_disability": 1,
    "not_provided|Generalized_hypotonia|Gastrostomy_tube_feeding_in_infancy|Decreased_activity_of_mitochondrial_complex_I|Global_developmental_delay|Absent_speech|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 1,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided": 1,
    "Global_developmental_delay|Decreased_head_circumference|Atypical_behavior|Sleep_abnormality|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Neurodevelopmental_disorder": 1,
    "Autism_spectrum_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome": 1,
    "Inborn_genetic_diseases|ASXL3-related_disorder": 2,
    "not_specified|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|ASXL3-related_disorder|Inborn_genetic_diseases": 1,
    "ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_provided|ASXL3-related_disorder": 1,
    "ASXL3-related_disorder|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Vascular_disorder": 1,
    "not_provided|Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|not_specified": 1,
    "ASXL3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|ASXL3-related_disorder": 1,
    "Intellectual_disability|not_provided|ASXL3-related_disorder": 1,
    "Severe_feeding_difficulties-failure_to_thrive-microcephaly_due_to_ASXL3_deficiency_syndrome|Intellectual_disability|not_provided|ASXL3-related_disorder": 1,
    "Inborn_genetic_diseases|Autism_spectrum_disorder|not_provided": 1,
    "ASXL3-related_disorder|not_specified": 1,
    "not_provided|not_specified|Left_ventricular_noncompaction_1": 4,
    "Left_ventricular_noncompaction_1|Left_ventricular_noncompaction_cardiomyopathy": 2,
    "Left_ventricular_noncompaction_1|Primary_dilated_cardiomyopathy|Ventricular_tachycardia|Left_ventricular_noncompaction_cardiomyopathy|DTNA-related_disorder|not_specified": 1,
    "Left_ventricular_noncompaction_1|not_specified|not_provided": 4,
    "Left_ventricular_noncompaction_1|not_specified": 31,
    "not_specified|not_provided|Left_ventricular_noncompaction_1": 8,
    "not_provided|Left_ventricular_noncompaction_1|not_specified": 4,
    "Left_ventricular_noncompaction_1|Noncompaction_cardiomyopathy|Cardiac_arrhythmia": 1,
    "Left_ventricular_noncompaction_1|not_provided": 14,
    "not_specified|DTNA-related_disorder|Left_ventricular_noncompaction_1": 1,
    "not_provided|Left_ventricular_noncompaction_1": 15,
    "not_provided|Left_ventricular_noncompaction_1|Cardiomyopathy|not_specified": 1,
    "not_specified|Left_ventricular_noncompaction_1|not_provided": 3,
    "not_provided|DTNA-related_disorder|not_specified|Left_ventricular_noncompaction_1": 2,
    "not_specified|Left_ventricular_noncompaction_1|See_cases": 1,
    "Dilated_cardiomyopathy_1HH|Left_ventricular_noncompaction_1": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided": 1,
    "not_specified|Left_ventricular_noncompaction_1": 16,
    "Left_ventricular_noncompaction_1|not_provided|DTNA-related_disorder": 2,
    "Left_ventricular_noncompaction_1|not_provided|not_specified": 4,
    "not_provided|DTNA-related_disorder|Left_ventricular_noncompaction_1": 1,
    "DTNA-related_disorder": 6,
    "Left_ventricular_noncompaction_1|DTNA-related_disorder|not_provided": 1,
    "not_specified|DTNA-related_disorder|Left_ventricular_noncompaction_1|not_provided": 1,
    "Left_ventricular_noncompaction_1|not_provided|DTNA-related_disorder|not_specified": 1,
    "Left_ventricular_noncompaction_1|DTNA-related_disorder": 2,
    "not_specified|Left_ventricular_noncompaction_1|DTNA-related_disorder": 1,
    "DTNA-related_disorder|not_specified|not_provided": 1,
    "not_specified|Left_ventricular_noncompaction_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "DTNA-related_disorder|Left_ventricular_noncompaction_1": 3,
    "DTNA-related_disorder|not_specified|not_provided|Left_ventricular_noncompaction_1": 5,
    "Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_1|not_specified|not_provided": 1,
    "Left_ventricular_noncompaction_1|DTNA-related_disorder|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Systolic_heart_failure|not_specified|not_provided|Left_ventricular_noncompaction_1": 1,
    "Left_ventricular_noncompaction_1|Congenital_heart_disease": 1,
    "MYOPATHY_WITH_MYALGIA|_INCREASED_SERUM_CREATINE_KINASE|_WITHOUT_EPISODIC_RHABDOMYOLYSIS_2|Myopathy_with_myalgia|_increased_serum_creatine_kinase|_and_with_or_without_episodic_rhabdomyolysis": 1,
    "Myopathy_with_myalgia|_increased_serum_creatine_kinase|_and_with_or_without_episodic_rhabdomyolysis_2": 1,
    "not_specified|not_provided|Left_ventricular_noncompaction_1|Hypertrophic_cardiomyopathy": 1,
    "not_provided|DTNA-related_disorder|Left_ventricular_noncompaction_1|not_specified": 1,
    "not_specified|Cardiomyopathy|Left_ventricular_noncompaction_1": 1,
    "not_provided|Left_ventricular_noncompaction_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiomyopathy|Left_ventricular_noncompaction_1": 1,
    "Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_1|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_1|DTNA-related_disorder": 1,
    "Meniere_disease|not_provided|Left_ventricular_noncompaction_1": 1,
    "DTNA-related_disorder|Left_ventricular_noncompaction_1|not_provided": 1,
    "Skin_creases|_congenital_symmetric_circumferential|_2|not_provided": 1,
    "MAPRE2-related_disorder": 3,
    "Skin_creases|_congenital_symmetric_circumferential|_2": 9,
    "not_provided|MAPRE2-related_disorder": 1,
    "Developmental_disorder|Skin_creases|_congenital_symmetric_circumferential|_2": 1,
    "Skin_creases|_congenital_symmetric_circumferential|_2|Inborn_genetic_diseases": 1,
    "ELP2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_58": 17,
    "ELP2-related_disorder": 6,
    "See_cases|Intellectual_disability|_autosomal_recessive_58|not_provided": 1,
    "ELP2-related_disorder|not_provided": 2,
    "not_provided|Intellectual_disability|_profound|Intellectual_disability|_autosomal_recessive_58": 1,
    "not_provided|ELP2-related_disorder": 5,
    "not_provided|Intellectual_disability|_autosomal_recessive_58": 2,
    "not_provided|ELP2-related_disorder|Intellectual_disability|_autosomal_recessive_58|Inborn_genetic_diseases": 1,
    "not_provided|ELP2-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_profound": 2,
    "Intellectual_disability|_autosomal_recessive_58|not_provided|ELP2-related_disorder|Intellectual_disability|_profound": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_58|Inborn_genetic_diseases": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_58|Intellectual_disability|_profound": 1,
    "Inborn_genetic_diseases|ELP2-related_disorder": 1,
    "MOCOS-related_disorder|not_provided": 1,
    "Xanthinuria_type_II|not_specified": 32,
    "MOCOS-related_disorder": 2,
    "Xanthinuria_type_II|not_provided|not_specified": 1,
    "Xanthinuria_type_II|MOCOS-related_disorder": 2,
    "not_specified|not_provided|Xanthinuria_type_II": 1,
    "not_specified|Xanthinuria_type_II|not_provided|MOCOS-related_disorder": 2,
    "MOCOS-related_disorder|Xanthinuria_type_II": 4,
    "Xanthinuria_type_II|not_specified|not_provided": 1,
    "not_provided|Xanthinuria_type_II|not_specified": 1,
    "Xanthinuria_type_II|Autism_spectrum_disorder": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic|_28|Inborn_genetic_diseases|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_hypertrophic|_28": 26,
    "FHOD3-related_disorder": 9,
    "Cardiovascular_phenotype|FHOD3-related_disorder|not_provided": 1,
    "FHOD3-related_disorder|Cardiovascular_phenotype": 1,
    "FHOD3-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|Cardiomyopathy|_familial_hypertrophic|_28": 3,
    "Cardiomyopathy|_familial_hypertrophic|_28|FHOD3-related_disorder": 1,
    "not_specified|FHOD3-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Cardiomyopathy|_familial_hypertrophic|_28": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_familial_hypertrophic|_28": 1,
    "Cardiomyopathy|_familial_hypertrophic|_28|not_provided": 2,
    "Hypertrophic_cardiomyopathy|FHOD3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cardiovascular_phenotype|Cardiomyopathy|_familial_hypertrophic|_28|FHOD3-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_specified|Cardiomyopathy|_familial_hypertrophic|_28|not_provided": 1,
    "FHOD3-related_disorder|Inborn_genetic_diseases": 1,
    "FHOD3-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|FHOD3-related_disorder": 1,
    "not_specified|Cardiomyopathy|_familial_hypertrophic|_28": 1,
    "Inborn_genetic_diseases|FHOD3-related_disorder": 1,
    "Cardiomyopathy|_familial_hypertrophic|_28|Inborn_genetic_diseases": 1,
    "KIAA1328-related_disorder": 1,
    "CELF4-related_disorder": 8,
    "not_provided|CELF4-related_disorder": 1,
    "CELF4-related_disorder|not_provided": 1,
    "Developmental_disorder|Neurodevelopmental_disorder": 1,
    "not_provided|Schinzel-Giedion_syndrome": 15,
    "not_provided|Intellectual_disability|_autosomal_dominant_29": 12,
    "Inborn_genetic_diseases|not_provided|Schinzel-Giedion_syndrome": 1,
    "SETBP1-related_disorder|not_provided": 22,
    "Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29|not_provided": 2,
    "Schinzel-Giedion_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_29": 49,
    "Intellectual_disability|_autosomal_dominant_29|not_provided": 8,
    "not_provided|SETBP1-related_disorder": 14,
    "Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome": 5,
    "SETBP1-related_disorder": 28,
    "Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29": 6,
    "not_provided|Schinzel-Giedion_syndrome|not_specified": 2,
    "not_provided|not_specified|Schinzel-Giedion_syndrome": 4,
    "not_provided|Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome": 3,
    "Intellectual_disability|_autosomal_dominant_29|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29": 3,
    "SETBP1-related_disorder|not_provided|Schinzel-Giedion_syndrome": 1,
    "SETBP1-related_disorder|not_specified|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Schinzel-Giedion_syndrome|not_provided": 1,
    "not_provided|SETBP1-related_disorder|Schinzel-Giedion_syndrome": 2,
    "SETBP1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|SETBP1-related_disorder|not_provided|Schinzel-Giedion_syndrome": 1,
    "Inborn_genetic_diseases|SETBP1-related_disorder|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_29|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_29|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome|not_provided|not_specified": 1,
    "SETBP1-related_disorder|Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome|not_specified|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_29|SETBP1-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_29|SETBP1-related_disorder|not_provided|Developmental_disorder": 1,
    "Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29": 1,
    "Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome|not_provided": 3,
    "SETBP1-related_disorder|Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome|not_provided|Intellectual_disability": 1,
    "not_specified|Schinzel-Giedion_syndrome|not_provided": 1,
    "Schinzel-Giedion_syndrome": 21,
    "Intellectual_disability|_autosomal_dominant_29|SETBP1-related_disorder": 1,
    "SETBP1-related_disorder|Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29|Inborn_genetic_diseases|not_provided": 1,
    "Schinzel-Giedion_syndrome|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_29|Inborn_genetic_diseases": 1,
    "Schinzel-Giedion_syndrome|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_dominant_29|not_provided|Schinzel-Giedion_syndrome": 1,
    "not_provided|SETBP1-related_disorder|not_specified": 2,
    "Schinzel-Giedion_syndrome|See_cases|not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_29": 1,
    "SETBP1-related_disorder|Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29|not_provided": 1,
    "Schinzel-Giedion_syndrome|SETBP1-related_disorder": 1,
    "SETBP1-related_disorder|Intellectual_disability|_autosomal_dominant_29|not_provided|Schinzel-Giedion_syndrome": 1,
    "Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|SETBP1-related_disorder|not_provided": 1,
    "Penile_hypospadias|Large_fontanelles|Teratoma|Cerebral_atrophy|Hydronephrosis|Midface_retrusion|Atrial_septal_defect|Abnormal_nail_morphology": 1,
    "SETBP1-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_29|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|SETBP1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_29|not_specified|Schinzel-Giedion_syndrome": 1,
    "SETBP1-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|not_provided|Schinzel-Giedion_syndrome": 3,
    "not_provided|SETBP1-related_disorder|Intellectual_disability|_autosomal_dominant_29": 1,
    "not_specified|Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|SETBP1-related_disorder": 1,
    "SETBP1-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome": 1,
    "not_provided|not_specified|SETBP1-related_disorder": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_dominant_29|Schinzel-Giedion_syndrome": 1,
    "SETBP1-related_disorder|Schinzel-Giedion_syndrome|not_provided": 1,
    "SETBP1-related_disorder|not_specified|not_provided|Schinzel-Giedion_syndrome": 1,
    "Delayed_speech_and_language_development|Seizure|Macrocephaly|Joint_laxity|Generalized_joint_hypermobility|not_provided|Intellectual_disability|_autosomal_dominant_29": 1,
    "not_provided|Schinzel-Giedion_syndrome|SETBP1-related_disorder": 1,
    "SETBP1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Schinzel-Giedion_syndrome|Intellectual_disability|_autosomal_dominant_29": 1,
    "Inborn_genetic_diseases|SETBP1-related_disorder": 1,
    "SLC14A1-related_disorder": 6,
    "Jk-null_variant": 2,
    "SLC14A1-related_disorder|Jk-null_variant": 1,
    "BLOOD_GROUP|_KIDD_SYSTEM": 2,
    "altered_red_cell_phenotype": 1,
    "KIDD_BLOOD_POLYMORPHISM_Jk(a)/Jk(b)|not_provided|SLC14A1-related_disorder": 1,
    "Jk-null_variant|_finnish_type": 1,
    "Vici_syndrome|not_specified|not_provided": 4,
    "Vici_syndrome|Inborn_genetic_diseases": 54,
    "Vici_syndrome": 1831,
    "Inborn_genetic_diseases|Vici_syndrome": 77,
    "not_specified|Vici_syndrome|not_provided": 1,
    "Vici_syndrome|not_provided": 26,
    "not_provided|Vici_syndrome|Limb-girdle_muscular_dystrophy|EPG5-related_disorder": 1,
    "Vici_syndrome|EPG5-related_disorder": 19,
    "EPG5-related_disorder|Vici_syndrome": 18,
    "not_provided|Vici_syndrome": 47,
    "EPG5-related_disorder": 6,
    "not_provided|Vici_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_provided|Vici_syndrome": 6,
    "Inborn_genetic_diseases|Vici_syndrome|not_specified|not_provided": 1,
    "Vici_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|not_provided|Vici_syndrome": 2,
    "EPG5-related_disorder|not_provided|Vici_syndrome": 6,
    "Vici_syndrome|not_provided|not_specified": 2,
    "not_specified|Vici_syndrome": 2,
    "Inborn_genetic_diseases|Vici_syndrome|Limb-girdle_muscular_dystrophy": 1,
    "Vici_syndrome|not_specified": 6,
    "Inborn_genetic_diseases|EPG5-related_disorder|not_provided|Vici_syndrome|not_specified": 1,
    "EPG5-related_disorder|not_specified|Vici_syndrome": 1,
    "Global_developmental_delay|Inborn_genetic_diseases|Vici_syndrome": 1,
    "Vici_syndrome|not_provided|Inborn_genetic_diseases": 5,
    "not_provided|not_specified|Vici_syndrome": 4,
    "not_provided|Vici_syndrome|EPG5-related_disorder": 6,
    "Inborn_genetic_diseases|Vici_syndrome|not_provided": 5,
    "Vici_syndrome|EPG5-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|not_specified|Vici_syndrome": 2,
    "Vici_syndrome|not_specified|EPG5-related_disorder": 1,
    "not_provided|EPG5-related_disorder": 1,
    "not_provided|EPG5-related_disorder|Vici_syndrome": 1,
    "EPG5-related_disorder|Vici_syndrome|not_provided": 2,
    "not_provided|Vici_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Vici_syndrome|not_specified|EPG5-related_disorder|Intellectual_disability": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Vici_syndrome": 1,
    "Inborn_genetic_diseases|EPG5-related_disorder|not_specified|not_provided|Vici_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Vici_syndrome": 3,
    "Syndromic_retinitis_pigmentosa": 2,
    "Vici_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "EPG5-related_disorder|Inborn_genetic_diseases|not_specified|Vici_syndrome|not_provided|Intellectual_disability": 1,
    "Vici_syndrome|not_provided|EPG5-related_disorder": 2,
    "Vici_syndrome|EPG5-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Vici_syndrome|not_provided": 1,
    "EPG5-related_disorder|Vici_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|EPG5-related_disorder|Inborn_genetic_diseases|Vici_syndrome": 1,
    "EPG5-related_disorder|Inborn_genetic_diseases|Vici_syndrome": 2,
    "Microcephaly|Vici_syndrome": 1,
    "EPG5-related_disorder|not_provided|not_specified|Vici_syndrome": 1,
    "not_specified|Vici_syndrome|EPG5-related_disorder": 1,
    "Inborn_genetic_diseases|Vici_syndrome|EPG5-related_disorder": 1,
    "ATP5F1A-related_disorder|not_provided": 2,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A": 2,
    "ATP5F1A-related_disorder": 5,
    "Combined_oxidative_phosphorylation_deficiency_22|not_provided": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A|not_provided": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4B": 1,
    "Combined_oxidative_phosphorylation_deficiency_22": 1,
    "not_provided|ATP5F1A-related_disorder": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A|not_provided|Lactic_acidosis": 1,
    "ATP5F1A-related_disorder|not_provided|Inborn_genetic_diseases|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A": 1,
    "Combined_oxidative_phosphorylation_deficiency_22|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4B|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_22|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4A|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_4B": 1,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency_22": 1,
    "ATP5F1A-related_disorder|not_provided|not_specified": 1,
    "not_provided|ATP5F1A-related_disorder|not_specified": 1,
    "ATP5F1A-related_disorder|not_specified|not_provided": 1,
    "HAUS1-related_condition": 1,
    "LOXHD1-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 7,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77": 321,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 82,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified": 14,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|not_specified": 20,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 102,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 36,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases|not_provided": 10,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases": 12,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases": 1,
    "concomitant_exotropia|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases": 3,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|Nonsyndromic_genetic_hearing_loss": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|Inborn_genetic_diseases": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|LOXHD1-related_disorder": 2,
    "LOXHD1-related_disorder|not_provided": 8,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases|not_specified": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified|not_provided": 12,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified": 18,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|Hearing_impairment|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77": 10,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77": 15,
    "LOXHD1-related_disorder|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases|not_specified": 3,
    "not_provided|not_specified|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "LOXHD1-related_disorder": 3,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|Hearing_loss|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77": 4,
    "not_provided|not_specified|LOXHD1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_77": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases": 4,
    "not_specified|LOXHD1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77": 3,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss": 2,
    "not_specified|Inborn_genetic_diseases|LOXHD1-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 14,
    "Hearing_impairment|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|LOXHD1-related_disorder": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 1,
    "LOXHD1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|not_specified": 2,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|LOXHD1-related_disorder": 2,
    "Hearing_loss|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "LOXHD1-related_disorder|not_specified|not_provided|VATER_association|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_77": 2,
    "LOXHD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 3,
    "LOXHD1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 3,
    "LOXHD1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|LOXHD1-related_disorder|Deafness|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77": 2,
    "LOXHD1-related_disorder|Rare_genetic_deafness|Inborn_genetic_diseases|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|LOXHD1-related_disorder|not_provided|not_specified": 1,
    "not_provided|LOXHD1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|LOXHD1-related_disorder|not_specified": 1,
    "not_specified|LOXHD1-related_disorder": 1,
    "not_specified|LOXHD1-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 2,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|not_specified|LOXHD1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77": 2,
    "LOXHD1-related_disorder|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified|not_provided": 1,
    "not_provided|LOXHD1-related_disorder": 8,
    "not_provided|LOXHD1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|Hearing_loss|_autosomal_recessive|Hearing_impairment|LOXHD1-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified|LOXHD1-related_disorder": 1,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|Hearing_impairment|not_specified|not_provided": 1,
    "Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided|Hearing_impairment": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|Hearing_impairment": 1,
    "not_provided|Stickler_syndrome|Inborn_genetic_diseases": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|LOXHD1-related_disorder": 1,
    "not_provided|not_specified|LOXHD1-related_disorder": 1,
    "not_provided|LOXHD1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|Variant_of_unknown_significance": 1,
    "Inborn_genetic_diseases|LOXHD1-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|LOXHD1-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77|Rare_genetic_deafness": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_77|LOXHD1-related_disorder|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|Hearing_impairment|not_provided": 1,
    "Deafness|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "LOXHD1-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_77": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_specified": 1,
    "LOXHD1-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_77|not_provided": 1,
    "KATNAL2-related_disorder": 21,
    "ELOA3P-related_condition": 3,
    "KATNAL2-related_disorder|not_provided": 1,
    "KATNAL2-related_disorder|not_specified": 6,
    "not_specified|KATNAL2-related_disorder": 2,
    "KATNAL2-related_disorder|not_specified|not_provided": 2,
    "See_cases|not_specified|KATNAL2-related_disorder": 1,
    "KATNAL2-related_autism|not_specified|KATNAL2-related_disorder": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|not_specified|IER3IP1-related_disorder|Epilepsy": 1,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome": 77,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome_1|Microcephaly|_epilepsy|_and_diabetes_syndrome": 3,
    "Inborn_genetic_diseases|Microcephaly|_epilepsy|_and_diabetes_syndrome": 3,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome|Inborn_genetic_diseases": 3,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome|IER3IP1-related_disorder|not_specified|not_provided": 1,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome|not_provided|IER3IP1-related_disorder|not_specified": 1,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome|Microcephaly|_epilepsy|_and_diabetes_syndrome_1": 2,
    "not_specified|Microcephaly|_epilepsy|_and_diabetes_syndrome": 1,
    "Microcephaly|_epilepsy|_and_diabetes_syndrome_1|not_provided|Microcephaly|_epilepsy|_and_diabetes_syndrome": 1,
    "Intellectual_disability|_mild|Gait_ataxia|Dysarthria": 1,
    "Dysarthria|Intellectual_disability|_mild|Gait_ataxia": 1,
    "Loeys-Dietz_syndrome_6|not_provided": 1,
    "not_provided|Loeys-Dietz_syndrome_6": 4,
    "SMAD2-related_disorder": 4,
    "Loeys-Dietz_syndrome_6": 7,
    "SMAD2-related_cardiac_disorders": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|SMAD2-related_disorder": 1,
    "Congenital_heart_defects|_multiple_types|_8|_with_or_without_heterotaxy|Inborn_genetic_diseases": 1,
    "SMAD2-congenital_heart_disease_and_multiple_congenital_anomaly_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Loeys-Dietz_syndrome_6|Congenital_heart_defects|_multiple_types|_8|_with_or_without_heterotaxy|not_specified|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_8|_with_or_without_heterotaxy|not_provided": 1,
    "SMAD2-related_disorder|not_provided": 2,
    "not_provided|SMAD2-related_disorder": 3,
    "Congenital_heart_defects|_multiple_types|_8|_with_or_without_heterotaxy": 3,
    "not_provided|SMAD2-related_disorder|Inborn_genetic_diseases": 1,
    "Loeys-Dietz_syndrome_6|SMAD2-related_disorder": 1,
    "Inborn_genetic_diseases|SMAD2-related_disorder|not_provided": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_8|_with_or_without_heterotaxy": 1,
    "SMAD2-_related_Loeys-Dietz_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|SMAD2-related_disorder": 1,
    "SMAD7-related_disorder": 9,
    "Colorectal_cancer|_susceptibility_to|_3": 1,
    "not_provided|SMAD7-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_3|not_specified": 1,
    "Smith-McCort_dysplasia|Dyggve-Melchior-Clausen_syndrome": 7,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia|not_provided": 3,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia": 10,
    "Dyggve-Melchior-Clausen_syndrome|not_provided|Smith-McCort_dysplasia": 2,
    "not_provided|Dyggve-Melchior-Clausen_syndrome": 4,
    "DYM-related_disorder": 4,
    "not_provided|Smith-McCort_dysplasia|Dyggve-Melchior-Clausen_syndrome": 1,
    "not_provided|DYM-related_disorder|Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia": 1,
    "Dyggve-Melchior-Clausen_syndrome|not_provided|Inborn_genetic_diseases|Smith-McCort_dysplasia": 1,
    "Dyggve-Melchior-Clausen_syndrome|Connective_tissue_disorder|not_provided|Smith-McCort_dysplasia": 4,
    "Dyggve-Melchior-Clausen_syndrome": 24,
    "Smith-McCort_dysplasia_1": 1,
    "Dyggve-Melchior-Clausen_syndrome|not_provided": 4,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia_1": 1,
    "Smith-McCort_dysplasia|not_specified|not_provided|Dyggve-Melchior-Clausen_syndrome": 1,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia_1|not_provided": 2,
    "DYM-related_disorder|not_provided": 3,
    "not_provided|Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia": 1,
    "Inborn_genetic_diseases|DYM-related_disorder|not_provided": 1,
    "Dyggve-Melchior-Clausen_syndrome|not_provided|Smith-McCort_dysplasia|Inborn_genetic_diseases": 1,
    "DYM-related_disorder|Dyggve-Melchior-Clausen_syndrome": 1,
    "not_provided|DYM-related_disorder": 3,
    "DYM-related_disorder|Smith-McCort_dysplasia|Dyggve-Melchior-Clausen_syndrome": 1,
    "Inborn_genetic_diseases|Dyggve-Melchior-Clausen_syndrome": 1,
    "not_provided|Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia_1": 1,
    "DYM-related_disorder|Connective_tissue_disorder|not_provided|Smith-McCort_dysplasia_1|Dyggve-Melchior-Clausen_syndrome": 1,
    "DYM-related_disorder|not_specified|not_provided": 1,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia_1|Inborn_genetic_diseases|not_provided": 1,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia_1|not_provided|DYM-related_disorder": 1,
    "not_provided|Smith-McCort_dysplasia_1|DYM-related_disorder": 1,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia_1|Connective_tissue_disorder|not_provided": 1,
    "Dyggve-Melchior-Clausen_syndrome|DYM-related_disorder|Smith-McCort_dysplasia": 1,
    "Dyggve-Melchior-Clausen_syndrome|Smith-McCort_dysplasia|Inborn_genetic_diseases": 1,
    "Smith-McCort_dysplasia|not_provided|Dyggve-Melchior-Clausen_syndrome": 1,
    "Glycosylphosphatidylinositol_biosynthesis_defect_25|not_provided": 1,
    "High_forehead|Failure_to_thrive_in_infancy|Macrocytic_anemia|Attention_deficit_hyperactivity_disorder|Pancytopenia|Fetal_growth_restriction|Autism|Epicanthus|Small_for_gestational_age|Triangular_face": 1,
    "LIPG-related_disorder": 4,
    "not_provided|LIPG-related_disorder": 1,
    "LIPG-related_disorder|not_provided": 1,
    "Congenital_microvillous_atrophy": 200,
    "Diarrhea_with_Microvillus_Atrophy": 12,
    "not_provided|Congenital_microvillous_atrophy": 62,
    "Congenital_microvillous_atrophy|not_provided": 47,
    "not_provided|Diarrhea_with_Microvillus_Atrophy": 2,
    "Diarrhea_with_Microvillus_Atrophy|not_provided": 1,
    "MYO5B-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|MYO5B-related_disorder": 33,
    "MYO5B-related_disorder": 41,
    "Inborn_genetic_diseases|not_provided|Congenital_microvillous_atrophy": 4,
    "Congenital_microvillous_atrophy|Inborn_genetic_diseases|not_provided": 2,
    "MYO5B-related_disorder|not_provided": 43,
    "not_provided|Inborn_genetic_diseases|Congenital_microvillous_atrophy": 2,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_10|Inborn_genetic_diseases|Congenital_microvillous_atrophy": 1,
    "Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy|not_provided": 1,
    "Congenital_microvillous_atrophy|Cholestasis|_progressive_familial_intrahepatic|_10|not_provided": 3,
    "Inborn_genetic_diseases|Congenital_microvillous_atrophy|MYO5B-related_disorder|not_provided": 2,
    "MYO5B-related_disorder|Congenital_microvillous_atrophy|not_provided": 4,
    "Inborn_genetic_diseases|Cholestasis|_progressive_familial_intrahepatic|_10": 1,
    "not_provided|Inflammatory_bowel_disease_1|MYO5B-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|MYO5B-related_disorder": 2,
    "Congenital_microvillous_atrophy|Cholestasis|_progressive_familial_intrahepatic|_10|MYO5B-related_disorder|not_provided": 1,
    "not_specified|Congenital_microvillous_atrophy|not_provided": 5,
    "Inborn_genetic_diseases|Congenital_microvillous_atrophy|not_provided": 1,
    "not_provided|MYO5B-related_disorder|Inborn_genetic_diseases": 2,
    "MYO5B-related_disorder|Congenital_microvillous_atrophy|Cholestasis|_progressive_familial_intrahepatic|_10|not_provided": 1,
    "Inborn_genetic_diseases|MYO5B-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Congenital_microvillous_atrophy": 2,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy": 3,
    "not_provided|MYO5B-related_disorder|Congenital_microvillous_atrophy|Inborn_genetic_diseases": 1,
    "Congenital_microvillous_atrophy|MYO5B-related_disorder|not_provided": 3,
    "Congenital_microvillous_atrophy|not_provided|MYO5B-related_disorder": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_10": 14,
    "Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy|MYO5B-related_disorder|not_provided": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy|not_provided": 3,
    "Inborn_genetic_diseases|EBV-positive_nodal_T-_and_NK-cell_lymphoma|MYO5B-related_disorder|not_provided": 1,
    "not_specified|not_provided|Congenital_microvillous_atrophy": 4,
    "Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy|not_specified|Diarrhea_with_Microvillus_Atrophy|not_provided": 1,
    "not_provided|MYO5B-related_disorder|Congenital_microvillous_atrophy": 4,
    "MYO5B-related_disorder|Cholestasis|_progressive_familial_intrahepatic|_10|Inborn_genetic_diseases|not_provided": 1,
    "MYO5B-related_disorder|Inborn_genetic_diseases|Congenital_microvillous_atrophy|not_provided": 1,
    "MYO5B-related_disorder|not_provided|Congenital_microvillous_atrophy": 9,
    "Inborn_genetic_diseases|MYO5B-related_disorder|not_provided|Congenital_microvillous_atrophy": 2,
    "Diarrhea_with_Microvillus_Atrophy|MYO5B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy": 2,
    "not_provided|Congenital_microvillous_atrophy|MYO5B-related_disorder": 3,
    "Congenital_microvillous_atrophy|MYO5B-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Diarrhea_with_Microvillus_Atrophy": 1,
    "not_provided|Inborn_genetic_diseases|MYO5B-related_disorder": 2,
    "not_provided|Cholestasis|_progressive_familial_intrahepatic|_10": 2,
    "DIARRHEA_2|_WITH_MICROVILLUS_ATROPHY_AND_CHOLESTASIS": 4,
    "MYO5B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_microvillous_atrophy|not_specified": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_10|not_provided": 1,
    "MYO5B-related_disorder|not_specified|not_provided|Congenital_microvillous_atrophy": 1,
    "Cholestasis|_progressive_familial_intrahepatic|_10|Congenital_microvillous_atrophy|Inborn_genetic_diseases": 1,
    "Congenital_microvillous_atrophy|not_specified|not_provided": 1,
    "CFAP53-related_disorder": 2,
    "Heterotaxy|_visceral|_6|_autosomal": 43,
    "Inborn_genetic_diseases|Heterotaxy|_visceral|_6|_autosomal": 8,
    "not_provided|Heterotaxy|_visceral|_6|_autosomal|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Heterotaxy|_visceral|_6|_autosomal|not_provided": 1,
    "Heterotaxy|_visceral|_6|_autosomal|Inborn_genetic_diseases": 2,
    "not_specified|Heterotaxy|_visceral|_6|_autosomal": 1,
    "not_provided|not_specified|Heterotaxy|_visceral|_6|_autosomal": 4,
    "Heterotaxy|_visceral|_6|_autosomal|not_provided": 2,
    "not_specified|not_provided|Heterotaxy|_visceral|_6|_autosomal": 2,
    "Heterotaxy|not_provided": 2,
    "Heterotaxy|_visceral|_6|_autosomal|not_specified|not_provided": 4,
    "Heterotaxy|_visceral|_6|_autosomal|CFAP53-related_disorder|not_provided|not_specified": 1,
    "not_provided|Heterotaxy|_visceral|_6|_autosomal|not_specified": 1,
    "Dextrocardia|not_provided|Heterotaxy|_visceral|_6|_autosomal": 1,
    "CFAP53-related_disorder|Heterotaxy|_visceral|_6|_autosomal": 1,
    "Hypoplastic_left_heart_syndrome|Inborn_genetic_diseases": 1,
    "MBD1-related_disorder": 10,
    "not_provided|MBD1-related_disorder": 2,
    "MBD1-related_disorder|not_specified": 1,
    "MBD1-related_disorder|not_provided": 1,
    "not_specified|ME2-related_disorder": 1,
    "ME2-related_disorder": 3,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome": 18,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Myhre_syndrome|Juvenile_Polyposis": 11,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 30,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome": 13,
    "Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 37,
    "Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Juvenile_polyposis_syndrome|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 166,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Juvenile_polyposis_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 84,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 67,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 58,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 252,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 50,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 47,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 4,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified|not_provided": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "not_specified|Myhre_syndrome|Pulmonary_arterial_hypertension|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|SMAD4-related_disorder|Familial_pancreatic_carcinoma|Juvenile_polyposis_syndrome|not_provided|Carcinoma_of_pancreas": 1,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 8,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 40,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 19,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 13,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Pulmonary_hypertension|_primary|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 10,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 50,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 5,
    "Myhre_syndrome": 3,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 14,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 11,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Carcinoma_of_pancreas|Juvenile_polyposis_syndrome|Myhre_syndrome|Early_age_onset_of_sporadic_thoracic_aortic_dissections|Heritable_Thoracic_Aortic_Disease": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 10,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Familial_pancreatic_carcinoma|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 15,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 3,
    "SMAD4-related_disorder": 5,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 9,
    "Juvenile_polyposis_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided": 7,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD4-related_disorder|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Myhre_syndrome|Carcinoma_of_pancreas": 1,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Carcinoma_of_pancreas|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome|not_specified": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|SMAD4-related_disorder": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 18,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Myhre_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|not_specified": 3,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 5,
    "Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 28,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 3,
    "Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 2,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 19,
    "Heritable_Thoracic_Aortic_Disease|Juvenile_polyposis_syndrome|Heritable_thoracic_aortic_disease_without_juvenile_polyposis_and_hereditary_hemorrhagic_telangiectasia": 1,
    "Myhre_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 17,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 8,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|SMAD4-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_colon": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|Juvenile_polyposis_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome": 1,
    "SMAD4-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 2,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 3,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided": 3,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Juvenile_polyposis_syndrome|SMAD4-related_disorder": 3,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|not_provided": 1,
    "not_specified|not_provided|Myhre_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|SMAD4-related_disorder|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "not_specified|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_pancreatic_carcinoma|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified": 1,
    "not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD4-related_disorder|not_specified": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Myhre_syndrome|not_specified|not_provided": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 1,
    "SMAD4-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified": 2,
    "Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|SMAD4-related_disorder|not_provided": 1,
    "Carcinoma_of_pancreas|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Carcinoma_of_pancreas|Myhre_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified|not_provided": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified": 1,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 1,
    "not_specified|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 2,
    "not_specified|SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|not_provided|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|SMAD4-related_disorder": 1,
    "Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 4,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 2,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|SMAD4-related_disorder|Carcinoma_of_pancreas|Juvenile_polyposis_syndrome|Myhre_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_pancreatic_carcinoma|Myhre_syndrome|Carcinoma_of_pancreas|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_specified|not_provided": 1,
    "not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_of_stomach": 1,
    "Juvenile_polyposis_syndrome|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas": 1,
    "not_provided|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome": 1,
    "not_specified|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|SMAD4-related_disorder": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Juvenile_polyposis_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_pancreatic_carcinoma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Juvenile_polyposis_syndrome|Early_age_onset_of_sporadic_thoracic_aortic_dissections|Heritable_Thoracic_Aortic_Disease": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "Juvenile_polyposis_syndrome|SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided": 3,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided": 1,
    "Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|not_specified": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 4,
    "Juvenile_polyposis_syndrome|Myhre_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Myhre_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis_syndrome": 2,
    "not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_hemorrhagic_telangiectasia|not_specified|not_provided|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome": 1,
    "Juvenile_polyposis_syndrome|Nephroblastoma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SMAD4-related_disorder|Juvenile_polyposis_syndrome|not_specified|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 1,
    "not_provided|not_specified|Myhre_syndrome|Juvenile_polyposis_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|not_provided": 1,
    "SMAD4-related_disorder|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Juvenile_polyposis_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Juvenile_polyposis_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Juvenile_polyposis_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Myhre_syndrome|Familial_pancreatic_carcinoma": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|SMAD4-related_disorder": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 2,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|not_provided": 1,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_pancreatic_carcinoma|Juvenile_polyposis_syndrome|Myhre_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 2,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Vascular_dementia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|SMAD4-related_disorder|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Carcinoma_of_pancreas|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified|not_provided|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|SMAD4-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Isolated_thoracic_aortic_aneurysm|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Carcinoma_of_pancreas|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Myhre_syndrome": 1,
    "Juvenile_polyposis_syndrome|Carcinoma_of_pancreas|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Malignant_tumor_of_breast": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified": 1,
    "Juvenile_polyposis_syndrome|Carcinoma_of_pancreas|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|not_provided": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Malignant_tumor_of_breast|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 2,
    "SMAD4-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Carcinoma_of_pancreas|Myhre_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_pancreatic_carcinoma|Myhre_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|Carcinoma_of_pancreas|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided|Carcinoma_of_colon": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 3,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 7,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|not_provided|SMAD4-related_disorder": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Gallbladder_cancer": 1,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Myhre_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 1,
    "Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis_syndrome|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 2,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Juvenile_polyposis_syndrome": 1,
    "not_specified|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Pulmonary_hypertension|_primary|_1": 1,
    "not_specified|SMAD4-related_disorder|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Myhre_syndrome|Carcinoma_of_pancreas|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Moyamoya_angiopathy|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Intellectual_disability": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|SMAD4-related_disorder|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome|Carcinoma_of_pancreas|Familial_aortopathy|not_provided|Familial_renal_glucosuria|Intellectual_disability|Neurodevelopmental_delay": 1,
    "Juvenile_polyposis_syndrome|SMAD4-related_disorder|not_provided|Myhre_syndrome": 1,
    "Juvenile_polyposis_syndrome|not_provided|Myhre_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|SMAD4-related_disorder|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Familial_pancreatic_carcinoma|Myhre_syndrome|Juvenile_polyposis_syndrome": 1,
    "not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Myhre_syndrome": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis_syndrome|Myhre_syndrome|Familial_pancreatic_carcinoma|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "SMAD4-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Gastrointestinal_polyposis": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome": 1,
    "SMAD4-related_disorder|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|SMAD4-related_disorder": 1,
    "Juvenile_polyposis_syndrome|Colorectal_cancer": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Myhre_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome": 1,
    "Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Juvenile_polyposis_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|SMAD4-related_disorder|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified": 1,
    "SMAD4-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|not_specified|not_provided|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Myhre_syndrome": 1,
    "not_provided|not_specified|SMAD4-related_disorder|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Hereditary_cancer-predisposing_syndrome|Juvenile_polyposis_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Carcinoma_of_pancreas|Juvenile_polyposis_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 22,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_specified|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Myhre_syndrome|Juvenile_Polyposis": 1,
    "Myhre_syndrome|Juvenile_Polyposis|Telangiectasia|_hereditary_hemorrhagic|_type_1": 6,
    "Generalized_juvenile_polyposis/juvenile_polyposis_coli|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Myhre_syndrome": 1,
    "not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome": 2,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided|Myhre_syndrome": 1,
    "Myhre_syndrome|Telangiectasia|_hereditary_hemorrhagic|_type_1|Juvenile_Polyposis": 9,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Juvenile_Polyposis|not_provided|Myhre_syndrome": 2,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 2,
    "Myhre_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Lung_cancer|not_specified|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome": 1,
    "Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Myhre_syndrome|not_provided": 1,
    "Myhre_syndrome|not_provided|Juvenile_Polyposis|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Myhre_syndrome|Juvenile_Polyposis": 1,
    "Myhre_syndrome|Telangiectasia|_hereditary_hemorrhagic|_type_1|not_provided|Juvenile_Polyposis": 2,
    "Telangiectasia|_hereditary_hemorrhagic|_type_1|Juvenile_Polyposis|Myhre_syndrome": 3,
    "Myhre_syndrome|not_provided|Telangiectasia|_hereditary_hemorrhagic|_type_1|Juvenile_Polyposis": 1,
    "Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|not_provided": 1,
    "Juvenile_Polyposis|Myhre_syndrome|Telangiectasia|_hereditary_hemorrhagic|_type_1": 1,
    "Myhre_syndrome|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 2,
    "Myhre_syndrome|not_provided|Juvenile_polyposis/hereditary_hemorrhagic_telangiectasia_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "DCC-related_disorder": 25,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2": 3,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|not_provided|Mirror_movements_1": 5,
    "DCC-related_disorder|not_provided|Malignant_tumor_of_esophagus|Mirror_movements_1|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|Colorectal_cancer": 1,
    "Mirror_movements_1": 23,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|not_provided|DCC-related_disorder|Mirror_movements_1": 1,
    "Esophageal_carcinoma|_somatic": 1,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|Mirror_movements_1": 1,
    "not_provided|Corpus_callosum|_agenesis_of|Mirror_movements_1": 1,
    "Mirror_movements_1|Corpus_callosum|_agenesis_of": 4,
    "Malignant_tumor_of_esophagus|Mirror_movements_1|Colorectal_cancer|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|not_provided": 1,
    "not_provided|Mirror_movements_1": 3,
    "Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|DCC-related_disorder|not_provided": 1,
    "not_provided|Mirror_movements_1|Amenorrhea": 1,
    "Inborn_genetic_diseases|DCC-related_disorder|not_provided": 1,
    "Mirror_movements_1_and/or_agenesis_of_the_corpus_callosum": 1,
    "Corpus_callosum|_agenesis_of": 2,
    "Malignant_tumor_of_esophagus|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|Colorectal_cancer|Mirror_movements_1|DCC-related_disorder|not_provided": 1,
    "DCC-related_disorder|not_specified|not_provided|Mirror_movements_1": 1,
    "not_provided|Colorectal_cancer|Mirror_movements_1|Gaze_palsy|_familial_horizontal|_with_progressive_scoliosis|_2|Malignant_tumor_of_esophagus": 1,
    "not_specified|Corpus_callosum|_agenesis_of|Autism_spectrum_disorder": 1,
    "not_provided|Mirror_movements_1_and/or_agenesis_of_the_corpus_callosum": 1,
    "not_specified|Mirror_movements_1_and/or_agenesis_of_the_corpus_callosum": 1,
    "Colorectal_cancer|Inborn_genetic_diseases": 1,
    "not_provided|DCC-related_disorder": 1,
    "Pitt-Hopkins_syndrome": 678,
    "Pitt-Hopkins_syndrome|not_provided": 41,
    "not_provided|Pitt-Hopkins_syndrome": 49,
    "Pitt-Hopkins_syndrome|not_specified": 20,
    "not_provided|Pitt-Hopkins_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_3|not_specified": 2,
    "Corneal_dystrophy|_Fuchs_endothelial|_3|Pitt-Hopkins_syndrome": 7,
    "not_specified|not_provided|Pitt-Hopkins_syndrome": 4,
    "Inborn_genetic_diseases|Pitt-Hopkins_syndrome": 9,
    "not_specified|not_provided|Corneal_dystrophy|_Fuchs_endothelial|_3|Inborn_genetic_diseases|Pitt-Hopkins_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Pitt-Hopkins_syndrome": 9,
    "not_specified|Pitt-Hopkins_syndrome": 12,
    "Inborn_genetic_diseases|not_provided|Pitt-Hopkins_syndrome": 2,
    "Pitt-Hopkins_syndrome|Microcephaly": 1,
    "TCF4-related_disorder": 11,
    "Pitt-Hopkins_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_3": 5,
    "Severe_intellectual_deficiency|not_provided|Pitt-Hopkins_syndrome|Inborn_genetic_diseases": 1,
    "TCF4-related_disorder|Inborn_genetic_diseases|Corneal_dystrophy|_Fuchs_endothelial|_3|Pitt-Hopkins_syndrome|not_provided|Microcephaly": 1,
    "not_provided|Global_developmental_delay|Pitt-Hopkins_syndrome": 1,
    "TCF4-related_disorder|Inborn_genetic_diseases|Pitt-Hopkins_syndrome|not_provided": 1,
    "Pitt-Hopkins_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Global_developmental_delay|Cerebral_hypoplasia|Pitt-Hopkins_syndrome": 1,
    "not_provided|Pitt-Hopkins_syndrome|TCF4-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Pitt-Hopkins_syndrome": 1,
    "Pitt-Hopkins_syndrome|not_provided|TCF4-related_disorder|Inborn_genetic_diseases": 1,
    "TCF4-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Pitt-Hopkins_syndrome|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|Pitt-Hopkins_syndrome": 2,
    "Pitt-Hopkins_syndrome|Inborn_genetic_diseases": 7,
    "not_specified|not_provided|Pitt-Hopkins_syndrome|See_cases": 1,
    "Inborn_genetic_diseases|not_specified|Pitt-Hopkins_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Pitt-Hopkins_syndrome": 1,
    "Pitt-Hopkins_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "TCF4-related_disorder|Pitt-Hopkins_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Pitt-Hopkins_syndrome|not_specified|not_provided": 3,
    "Pitt-Hopkins_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_3|not_provided": 1,
    "not_specified|Pitt-Hopkins_syndrome|not_provided|Oculomotor_apraxia": 1,
    "Pitt-Hopkins_syndrome|TCF4-related_disorder": 3,
    "not_specified|Pitt-Hopkins_syndrome|TCF4-related_disorder": 1,
    "TCF4-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Pitt-Hopkins_syndrome": 1,
    "not_specified|Pitt-Hopkins_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_3": 1,
    "Pitt-Hopkins_syndrome|TCF4-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|TCF4-related_disorder|Pitt-Hopkins_syndrome": 1,
    "Pitt-Hopkins_syndrome|not_provided|not_specified|Corneal_dystrophy|_Fuchs_endothelial|_3": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_3": 2,
    "TCF4-related_disorder|Inborn_genetic_diseases|Pitt-Hopkins_syndrome": 1,
    "Pitt-Hopkins_syndrome|not_provided|Corneal_dystrophy|_Fuchs_endothelial|_3": 1,
    "not_provided|Pitt-Hopkins_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Pitt-Hopkins_syndrome|not_specified": 1,
    "TCF4-related_disorder|not_provided": 1,
    "Pitt-Hopkins_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_3|not_provided|Intellectual_disability": 1,
    "Neurodevelopmental_disorder|not_provided|Pitt-Hopkins_syndrome|Intellectual_disability": 1,
    "TCF4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Pitt-Hopkins_syndrome": 1,
    "Short_nose|Stereotypic_movement_disorder|Global_developmental_delay|Anteverted_nares|Feeding_difficulties_in_infancy|Epicanthus|Drooling|Pitt-Hopkins_syndrome": 1,
    "Inborn_genetic_diseases|Pitt-Hopkins_syndrome|not_provided": 1,
    "not_provided|Autism_spectrum_disorder|Pitt-Hopkins_syndrome": 1,
    "not_specified|Pitt-Hopkins_syndrome|Inborn_genetic_diseases": 1,
    "TCF4-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TCF4-related_disorder|not_provided|Pitt-Hopkins_syndrome": 1,
    "Pyloric_stenosis|Esophageal_atresia|Pitt-Hopkins_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Pitt-Hopkins_syndrome|not_provided": 1,
    "not_specified|TCF4-related_disorder": 1,
    "Inborn_genetic_diseases|Congenital_myopathy|not_specified|Pitt-Hopkins_syndrome": 1,
    "Pitt-Hopkins_syndrome|TCF4-related_disorder|not_specified": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Pitt-Hopkins_syndrome": 1,
    "Seizure|Pitt-Hopkins_syndrome": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_3|not_provided": 1,
    "WDR7-related_disorder": 2,
    "Protoporphyria|_erythropoietic|_1": 120,
    "Protoporphyria|_erythropoietic|_1|not_provided": 28,
    "not_provided|Protoporphyria|_erythropoietic|_1": 7,
    "FECH-related_disorder": 4,
    "FECH-related_disorder|not_provided": 3,
    "Protoporphyria|_erythropoietic|_1|not_provided|FECH-related_disorder": 1,
    "Autosomal_erythropoietic_protoporphyria": 2,
    "not_provided|FECH-related_disorder": 3,
    "not_specified|Protoporphyria|_erythropoietic|_1|not_provided": 2,
    "Protoporphyria|_erythropoietic|_1|FECH-related_disorder|not_provided": 1,
    "not_provided|FECH-related_disorder|Protoporphyria|_erythropoietic|_1": 1,
    "Protoporphyria|_erythropoietic|_1|FECH-related_disorder": 1,
    "not_provided|not_specified|Protoporphyria|_erythropoietic|_1|See_cases": 1,
    "Inborn_genetic_diseases|FECH-related_disorder": 1,
    "Autosomal_erythropoietic_protoporphyria|not_provided|Protoporphyria|_erythropoietic|_1|Jaundice|Erythema": 1,
    "not_specified|not_provided|Protoporphyria|_erythropoietic|_1": 1,
    "not_provided|Protoporphyria|_erythropoietic|_1|Inborn_genetic_diseases": 1,
    "not_provided|Jaundice|Erythema|not_specified|Protoporphyria|_erythropoietic|_1": 1,
    "not_provided|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities": 2,
    "Developmental_disorder|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_epilepsy|_and_gait_abnormalities|Neurodevelopmental_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_epilepsy|_and_gait_abnormalities": 9,
    "Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities": 21,
    "NARS1-related_disorder": 6,
    "Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities|not_provided": 3,
    "not_provided|not_specified|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities": 1,
    "NARS1-related_disorder|not_provided|not_specified": 1,
    "not_specified|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities|Neurodevelopmental_disorder|not_provided|See_cases": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_epilepsy|_and_gait_abnormalities": 2,
    "not_specified|Neurodevelopmental_disorder_with_microcephaly|_impaired_language|_and_gait_abnormalities": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_1|not_specified": 5,
    "not_provided|Inborn_genetic_diseases|ATP8B1-related_disorder": 2,
    "not_provided|ATP8B1-related_disorder": 12,
    "not_provided|not_specified|Progressive_familial_intrahepatic_cholestasis_type_1|ATP8B1-related_disorder": 1,
    "ATP8B1-related_disorder": 47,
    "Inborn_genetic_diseases|ATP8B1-related_disorder|not_provided": 2,
    "ATP8B1-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 3,
    "ATP8B1-related_disorder|not_provided": 21,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1|not_specified": 2,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1|not_specified|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1": 30,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|not_provided": 4,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1": 2,
    "Progressive_familial_intrahepatic_cholestasis|not_provided": 6,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1": 6,
    "ATP8B1-related_disorder|Inborn_genetic_diseases|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|not_specified|not_provided": 1,
    "not_provided|not_specified|Progressive_familial_intrahepatic_cholestasis_type_1": 2,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1|not_specified": 1,
    "not_specified|ATP8B1-related_disorder": 2,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "Inborn_genetic_diseases|Progressive_familial_intrahepatic_cholestasis_type_1": 2,
    "not_specified|Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 1,
    "not_provided|not_specified|ATP8B1-related_disorder": 4,
    "not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 5,
    "Progressive_familial_intrahepatic_cholestasis|Benign_recurrent_intrahepatic_cholestasis_type_1": 2,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|ATP8B1-related_disorder": 1,
    "ATP8B1-related_disorder|not_provided|not_specified": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided|Progressive_familial_intrahepatic_cholestasis|Cholestasis|_intrahepatic|_of_pregnancy|_1|ATP8B1-related_disorder": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_provided|not_specified": 2,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis|ATP8B1-related_disorder|not_provided": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_1": 5,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_1|Inborn_genetic_diseases": 1,
    "not_provided|ATP8B1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Benign_recurrent_intrahepatic_cholestasis_type_1": 6,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Intrahepatic_cholestasis_with_episodic_jaundice": 1,
    "not_provided|Inborn_genetic_diseases|Progressive_familial_intrahepatic_cholestasis_type_1": 2,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "not_specified|not_provided|ATP8B1-related_disorder": 2,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|not_provided|Progressive_familial_intrahepatic_cholestasis": 1,
    "Progressive_familial_intrahepatic_cholestasis|ATP8B1-related_disorder|Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Benign_recurrent_intrahepatic_cholestasis_type_1|not_provided": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1": 2,
    "ATP8B1-related_disorder|not_specified": 1,
    "ATP8B1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided": 2,
    "Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|not_specified": 1,
    "not_provided|ATP8B1-related_disorder|Progressive_familial_intrahepatic_cholestasis_type_1": 2,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|Familial_intrahepatic_cholestasis_type_1|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|not_provided|ATP8B1-related_disorder": 1,
    "not_provided|Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|Benign_recurrent_intrahepatic_cholestasis_type_1": 1,
    "ATP8B1-related_disorder|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_specified|not_provided|ATP8B1-related_disorder": 1,
    "Inborn_genetic_diseases|ATP8B1-related_disorder": 2,
    "Cholestasis|_intrahepatic|_of_pregnancy|_1|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis|Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|not_provided": 2,
    "Inborn_genetic_diseases|Benign_recurrent_intrahepatic_cholestasis_type_1|ATP8B1-related_disorder": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|ATP8B1-related_disorder|not_specified|not_provided": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_1|not_provided": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_specified|ATP8B1-related_disorder|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|ATP8B1-related_disorder|not_provided": 1,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_1|ATP8B1-related_disorder|not_provided": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "Progressive_familial_intrahepatic_cholestasis|Progressive_familial_intrahepatic_cholestasis_type_1|not_provided|ATP8B1-related_disorder": 1,
    "Benign_recurrent_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis": 1,
    "ATP8B1-related_disorder|not_specified|not_provided|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "not_specified|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "not_provided|not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_provided|not_specified|ATP8B1-related_disorder|Benign_recurrent_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "Familial_intrahepatic_cholestasis_type_1|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|not_provided|Inborn_genetic_diseases|Alagille_syndrome|_ATP8B1_related": 1,
    "ATP8B1-related_disorder|not_provided|Benign_recurrent_intrahepatic_cholestasis_type_1": 1,
    "Progressive_familial_intrahepatic_cholestasis_type_1|Cholestasis|_intrahepatic|_of_pregnancy|_1|not_provided|not_specified": 1,
    "ATP8B1-related_disorder|not_provided|not_specified|Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_2|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1": 1,
    "ATP8B1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "Cholestasis|_intrahepatic|_of_pregnancy|_1|Progressive_familial_intrahepatic_cholestasis_type_1|Benign_recurrent_intrahepatic_cholestasis_type_1|not_specified|not_provided": 1,
    "ATP8B1-related_disorder|not_provided|Cholestasis|_intrahepatic|_of_pregnancy|_1": 1,
    "not_specified|Progressive_familial_intrahepatic_cholestasis_type_1": 1,
    "NEDD4L-related_disorder|not_provided": 6,
    "Periventricular_nodular_heterotopia_7": 23,
    "not_provided|Periventricular_nodular_heterotopia_7": 24,
    "Periventricular_nodular_heterotopia_7|not_provided": 37,
    "not_provided|Periventricular_nodular_heterotopia_7|NEDD4L-related_disorder": 2,
    "not_provided|NEDD4L-related_disorder": 8,
    "Periventricular_nodular_heterotopia_7|not_specified|not_provided": 3,
    "NEDD4L-related_disorder": 8,
    "not_provided|NEDD4L-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|NEDD4L-related_disorder": 1,
    "not_provided|Periventricular_nodular_heterotopia_7|Intellectual_disability": 1,
    "NEDD4L-related_disorder|Periventricular_nodular_heterotopia_7|not_provided": 4,
    "Periventricular_nodular_heterotopia_7|not_provided|Inborn_genetic_diseases": 1,
    "Periventricular_nodular_heterotopia_7|NEDD4L-related_disorder|not_provided": 1,
    "NEDD4L-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Periventricular_nodular_heterotopia_7|Inborn_genetic_diseases|not_provided": 2,
    "Intellectual_disability|Periventricular_nodular_heterotopia_7": 1,
    "NEDD4L-related_disorder|not_specified": 1,
    "not_provided|Periventricular_nodular_heterotopia_7|Inborn_genetic_diseases": 2,
    "Periventricular_nodular_heterotopia_7|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Periventricular_nodular_heterotopia_7|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Periventricular_nodular_heterotopia_7|not_provided": 1,
    "Periventricular_nodular_heterotopia_7|Periventricular_nodular_heterotopia_with_syndactyly|_cleft_palate_and_developmental_delay": 2,
    "not_provided|Chromosome_5Q14.3_deletion_syndrome|_distal|Periventricular_nodular_heterotopia_with_syndactyly|_cleft_palate_and_developmental_delay|Periventricular_nodular_heterotopia_7": 1,
    "Intellectual_disability|Periventricular_nodular_heterotopia_7|Periventricular_nodular_heterotopia_with_syndactyly|_cleft_palate_and_developmental_delay|not_provided": 1,
    "ALPK2-related_disorder": 58,
    "not_specified|ALPK2-related_disorder": 14,
    "not_specified|ALPK2-related_disorder|not_provided": 2,
    "ALPK2-related_disorder|not_specified": 10,
    "not_specified|not_provided|ALPK2-related_disorder": 2,
    "not_provided|Combined_immunodeficiency_due_to_MALT1_deficiency": 8,
    "Combined_immunodeficiency_due_to_MALT1_deficiency": 341,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_MALT1_deficiency": 13,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|MALT1-related_disorder": 1,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|not_provided": 14,
    "Inborn_genetic_diseases|not_specified|Combined_immunodeficiency_due_to_MALT1_deficiency": 1,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|Inborn_genetic_diseases": 9,
    "MALT1-related_disorder|Combined_immunodeficiency_due_to_MALT1_deficiency": 4,
    "MALT1-related_disorder": 1,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|not_provided|MALT1-related_disorder": 2,
    "not_provided|Combined_immunodeficiency_due_to_MALT1_deficiency|not_specified": 1,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|not_specified": 1,
    "Combined_immunodeficiency_due_to_MALT1_deficiency|MALT1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Combined_immunodeficiency_due_to_MALT1_deficiency": 1,
    "MALT1-related_disorder|Combined_immunodeficiency_due_to_MALT1_deficiency|Inborn_genetic_diseases": 1,
    "Isolated_microphthalmia_3": 75,
    "not_provided|Isolated_microphthalmia_3": 15,
    "Isolated_microphthalmia_3|not_provided": 3,
    "Inborn_genetic_diseases|Isolated_microphthalmia_3": 3,
    "not_specified|not_provided|Isolated_microphthalmia_3": 1,
    "Isolated_microphthalmia_3|Inborn_genetic_diseases": 1,
    "RAX-related_disorder": 1,
    "Isolated_microphthalmia_3|RAX-related_disorder": 1,
    "Isolated_microphthalmia_3|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Isolated_microphthalmia_3|not_provided": 2,
    "not_provided|Isolated_microphthalmia_3|Inborn_genetic_diseases": 1,
    "Isolated_microphthalmia_3|RAX-related_disorder|not_provided": 1,
    "Isolated_microphthalmia_3|not_provided|RAX-related_disorder": 1,
    "Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1|not_provided": 10,
    "not_provided|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1": 4,
    "Inborn_genetic_diseases|not_provided|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1": 1,
    "LMAN1-related_disorder|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1": 2,
    "not_provided|not_specified|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1": 2,
    "Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1|LMAN1-related_disorder": 2,
    "Factor_V_deficiency|Hereditary_factor_VIII_deficiency_disease|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1": 1,
    "Inborn_genetic_diseases|LMAN1-related_disorder": 1,
    "LMAN1-related_disorder": 4,
    "not_provided|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1|not_specified": 1,
    "not_specified|Factor_V_and_factor_VIII|_combined_deficiency_of|_type_1|not_provided": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_provided": 31,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 20,
    "CCBE1-related_disorder|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|CCBE1-related_disorder": 1,
    "not_specified|Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_provided": 2,
    "CCBE1-related_disorder": 5,
    "not_specified|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 5,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 2,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|Inborn_genetic_diseases": 1,
    "CCBE1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_specified|not_provided": 1,
    "CCBE1-related_disorder|Inborn_genetic_diseases|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 2,
    "Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_provided": 1,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1|CCBE1-related_disorder": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_provided|CCBE1-related_disorder": 2,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_specified": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|CCBE1-related_disorder": 3,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|CCBE1-related_disorder|not_provided": 3,
    "CCBE1-related_disorder|Inborn_genetic_diseases": 2,
    "CCBE1-related_disorder|Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 3,
    "CCBE1-related_disorder|not_specified|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "not_provided|See_cases|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|not_provided|not_specified": 1,
    "not_provided|not_specified|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "not_specified|not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome_1|CCBE1-related_disorder": 1,
    "not_provided|Hennekam_lymphangiectasia-lymphedema_syndrome|Hennekam_lymphangiectasia-lymphedema_syndrome_1": 1,
    "Hennekam_lymphangiectasia-lymphedema_syndrome_1|Renal_tubular_acidosis|_distal|_4|_with_hemolytic_anemia": 1,
    "Autosomal_recessive_osteopetrosis_7": 13,
    "MC4R-related_disorder": 76,
    "MC4R-related_disorder|not_provided": 9,
    "MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20": 4,
    "not_provided|Obesity|not_specified|MC4R-related_disorder": 2,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity_due_to_melanocortin_4_receptor_deficiency|Obesity": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder|Obesity": 1,
    "not_provided|Obesity|Obesity_due_to_melanocortin_4_receptor_deficiency|MC4R-related_disorder": 1,
    "Obesity_due_to_melanocortin_4_receptor_deficiency": 2,
    "not_provided|MC4R-related_disorder": 5,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder": 2,
    "MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity_due_to_melanocortin_4_receptor_deficiency|not_provided|Obesity": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20": 20,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Monogenic_diabetes": 2,
    "Obesity_due_to_melanocortin_4_receptor_deficiency|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20": 1,
    "Obesity_due_to_melanocortin_4_receptor_deficiency|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided|MC4R-related_disorder|Obesity": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_specified|MC4R-related_disorder|not_provided": 1,
    "MC4R-related_disorder|Obesity|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity": 3,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder|Obesity_due_to_melanocortin_4_receptor_deficiency|Obesity": 1,
    "MC4R-related_disorder|not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20": 1,
    "not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_specified|Obesity": 1,
    "not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20": 3,
    "MC4R-related_disorder|Obesity": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided": 4,
    "MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity|_autosomal_dominant|not_provided|Obesity": 1,
    "MC4R-related_disorder|Monogenic_diabetes|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_specified|not_provided|Obesity": 1,
    "Monogenic_diabetes|not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder|Obesity": 1,
    "MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Monogenic_diabetes|not_provided": 2,
    "not_provided|MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20": 1,
    "not_specified|Inherited_obesity|MC4R-related_disorder|Monogenic_diabetes|Obesity|not_provided": 1,
    "not_specified|not_provided|Obesity": 1,
    "not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder|not_specified|Obesity": 1,
    "not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder": 1,
    "Obesity|MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided": 1,
    "not_provided|Obesity_due_to_melanocortin_4_receptor_deficiency|MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity": 1,
    "Obesity_due_to_melanocortin_4_receptor_deficiency|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided|MC4R-related_disorder": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity|not_provided": 1,
    "Obesity|MC4R-related_disorder|not_provided": 1,
    "not_provided|Monogenic_diabetes|MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity": 1,
    "Obesity|_autosomal_dominant|MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided|Obesity": 1,
    "MC4R-related_disorder|not_provided|not_specified": 1,
    "adipositas": 1,
    "not_specified|Obesity": 1,
    "not_provided|MC4R-related_disorder|Obesity|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity_due_to_melanocortin_4_receptor_deficiency": 1,
    "not_provided|Obesity_due_to_melanocortin_4_receptor_deficiency": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity|MC4R-related_disorder|not_provided": 1,
    "not_provided|not_specified|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity|MC4R-related_disorder|MC4R_POLYMORPHISM|OBESITY|_RESISTANCE_TO|Monogenic_diabetes": 1,
    "not_specified|not_provided|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder": 1,
    "not_provided|not_specified|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|MC4R-related_disorder": 1,
    "Obesity|_autosomal_dominant": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity_due_to_melanocortin_4_receptor_deficiency": 1,
    "Obesity|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|Obesity_due_to_melanocortin_4_receptor_deficiency|MC4R-related_disorder|Obesity|_autosomal_dominant|not_provided": 1,
    "BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_specified|not_provided|Obesity": 1,
    "Obesity_due_to_melanocortin_4_receptor_deficiency|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided|Schizophrenia|Obesity|See_cases": 1,
    "Obesity_due_to_melanocortin_4_receptor_deficiency|Obesity": 1,
    "MC4R-related_disorder|BODY_MASS_INDEX_QUANTITATIVE_TRAIT_LOCUS_20|not_provided": 1,
    "MC4R-related_disorder|Obesity|not_specified": 1,
    "Non-syndromic_syndactyly|not_specified": 1,
    "PIGN-related_disorder|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 891,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 47,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided|PIGN-related_disorder|Inborn_genetic_diseases": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases": 25,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases|not_provided": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided": 40,
    "Inborn_genetic_diseases|not_specified|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 25,
    "Inborn_genetic_diseases|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 9,
    "not_specified|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 3,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 10,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|PIGN-related_disorder": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases|not_provided": 4,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases": 1,
    "PIGN-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_specified": 2,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided|not_specified": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|PIGN-related_disorder|Inborn_genetic_diseases": 1,
    "PIGN-related_disorder|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided": 9,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_specified|not_provided": 1,
    "not_provided|not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_specified": 3,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|PIGN-related_disorder|not_provided": 1,
    "PIGN-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 5,
    "not_specified|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 4,
    "Inborn_genetic_diseases|not_provided|not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "not_provided|History_of_neurodevelopmental_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|PIGN-related_disorder|not_provided": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|PIGN-related_disorder|not_provided|Abnormal_brain_morphology": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_specified|not_provided": 1,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided|PIGN-related_disorder": 1,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Multiple_congenital_anomalies-hypotonia-seizures_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|Multiple_congenital_anomalies-hypotonia-seizures_syndrome": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1|PIGN-related_disorder|Inborn_genetic_diseases": 1,
    "PIGN-related_disorder": 1,
    "Neurodevelopmental_delay|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 1,
    "PIGN-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_1": 2,
    "Osteopetrosis|Bone_Paget_disease": 7,
    "not_specified|Osteopetrosis|not_provided|Bone_Paget_disease": 1,
    "Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset": 39,
    "Bone_Paget_disease|not_provided|Osteopetrosis|not_specified": 2,
    "not_provided|Autosomal_recessive_osteopetrosis_7|not_specified|Paget_disease_of_bone_2|_early-onset": 1,
    "Inborn_genetic_diseases|Autosomal_recessive_osteopetrosis_7|not_provided|Paget_disease_of_bone_2|_early-onset": 1,
    "not_provided|TNFRSF11A-related_disorder|Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset": 22,
    "not_provided|Paget_disease_of_bone_2|_early-onset": 1,
    "Familial_expansile_osteolysis|not_provided|Paget_disease_of_bone_2|_early-onset": 1,
    "Familial_expansile_osteolysis": 2,
    "Paget_disease_of_bone_2|_early-onset": 1,
    "Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset|not_provided": 1,
    "not_provided|Paget_disease_of_bone_2|_early-onset|Familial_expansile_osteolysis|Autosomal_recessive_osteopetrosis_7": 1,
    "TNFRSF11A-related_disorder|not_provided": 10,
    "Familial_expansile_osteolysis|not_provided": 2,
    "Autosomal_recessive_osteopetrosis_7|not_provided": 1,
    "Bone_Paget_disease|Increased_bone_mineral_density|not_specified|Osteopetrosis|not_provided": 1,
    "Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7|not_provided": 2,
    "not_specified|not_provided|Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset": 1,
    "not_specified|Osteopetrosis|Increased_bone_mineral_density|not_provided|Bone_Paget_disease": 1,
    "not_specified|not_provided|Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7": 1,
    "Paget_disease_of_bone_2|_early-onset|Familial_expansile_osteolysis|Autosomal_recessive_osteopetrosis_7|not_provided|Inborn_genetic_diseases": 1,
    "Bone_Paget_disease|TNFRSF11A-related_disorder|Autosomal_recessive_osteopetrosis_7|Familial_expansile_osteolysis|Paget_disease_of_bone_2|_early-onset|not_provided|Osteopetrosis": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_7": 1,
    "not_specified|Osteopetrosis|Bone_Paget_disease|Autosomal_recessive_osteopetrosis_7|Familial_expansile_osteolysis|not_provided": 1,
    "not_provided|Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset|TNFRSF11A-related_disorder": 1,
    "Paget_disease_of_bone_2|_early-onset|not_provided|Autosomal_recessive_osteopetrosis_7": 1,
    "not_provided|Familial_expansile_osteolysis|Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7": 1,
    "not_provided|TNFRSF11A-related_disorder|Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7": 1,
    "not_provided|Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7": 2,
    "TNFRSF11A-related_disorder": 3,
    "Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7|not_provided|TNFRSF11A-related_disorder": 1,
    "not_provided|Familial_expansile_osteolysis": 1,
    "Bone_Paget_disease|Osteopetrosis|not_provided": 2,
    "Increased_bone_mineral_density|not_provided|Autosomal_recessive_osteopetrosis_7|Paget_disease_of_bone_2|_early-onset": 1,
    "not_provided|Inborn_genetic_diseases|TNFRSF11A-related_disorder": 1,
    "Familial_expansile_osteolysis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|TNFRSF11A-related_disorder": 1,
    "Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7": 6,
    "not_provided|Inborn_genetic_diseases|Paget_disease_of_bone_2|_early-onset|Autosomal_recessive_osteopetrosis_7": 1,
    "Osteopetrosis|Bone_Paget_disease|not_provided": 1,
    "Bone_Paget_disease|Osteopetrosis": 1,
    "Attention_deficit_hyperactivity_disorder|Focal_impaired_awareness_seizure|Seizure": 1,
    "BCL2-related_disorder": 2,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_4": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_4": 5,
    "Erythrokeratodermia_variabilis_et_progressiva_4|not_provided": 1,
    "SERPINB7-related_disorder": 3,
    "Palmoplantar_keratoderma|_Nagashima_type": 4,
    "SERPINB7-related_disorder|not_provided": 2,
    "Palmoplantar_keratoderma|_Nagashima_type|not_provided": 2,
    "SERPINB7-related_disorder|Palmoplantar_keratoderma|_Nagashima_type|not_provided": 1,
    "not_provided|Palmoplantar_keratoderma|_Nagashima_type": 1,
    "Peeling_skin_syndrome_5": 3,
    "Peeling_skin_syndrome_5|not_provided": 4,
    "SERPINB8-related_disorder|not_provided": 3,
    "not_provided|SERPINB8-related_disorder": 1,
    "not_provided|Peeling_skin_syndrome_5": 2,
    "SERPINB8-related_disorder": 3,
    "CDH19-related_disorder": 17,
    "CDH19-related_disorder|not_provided": 2,
    "not_provided|CDH19-related_disorder": 1,
    "TMX3-related_disorder": 4,
    "Preeclampsia|Small_for_gestational_age|Normal_pregnancy|Large_for_gestational_age": 1,
    "RTTN-related_disorder": 17,
    "not_provided|not_specified|RTTN-related_disorder": 4,
    "not_provided|RTTN-related_disorder": 13,
    "Inborn_genetic_diseases|RTTN-related_disorder|not_specified|not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 1,
    "RTTN-related_disorder|not_provided": 13,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 29,
    "RTTN-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_provided": 13,
    "not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_specified": 2,
    "RTTN-related_disorder|not_specified|not_provided": 6,
    "Inborn_genetic_diseases|not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_specified": 1,
    "not_specified|not_provided|RTTN-related_disorder": 8,
    "Primary_microcephaly|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 3,
    "MICROCEPHALY|_SHORT_STATURE|_AND_POLYMICROGYRIA_WITH_SEIZURES": 1,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_specified|not_provided": 3,
    "not_specified|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_provided": 1,
    "not_provided|RTTN-related_disorder|not_specified": 5,
    "not_provided|MICROCEPHALY|_SHORT_STATURE|_AND_POLYMICROGYRIA_WITH_SEIZURES": 2,
    "RTTN-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "RTTN-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|RTTN-related_disorder": 1,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_provided|not_specified": 1,
    "not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 8,
    "Inborn_genetic_diseases|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_provided": 2,
    "not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|Inborn_genetic_diseases": 2,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|RTTN-related_disorder": 1,
    "Inborn_genetic_diseases|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 3,
    "RTTN-related_disorder|Microcephaly|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 3,
    "not_provided|Inborn_genetic_diseases|RTTN-related_disorder": 1,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|not_provided|RTTN-related_disorder|not_specified": 1,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|Primary_microcephaly": 1,
    "not_provided|RTTN-related_disorder|Inborn_genetic_diseases": 1,
    "RTTN-related_disorder|not_specified": 1,
    "Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|RTTN-related_disorder|not_specified": 1,
    "RTTN-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Disease_Association_NOS|not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 1,
    "not_provided|not_specified|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|MICROCEPHALY|_SHORT_STATURE|_AND_POLYMICROGYRIA_WITH_SEIZURES": 1,
    "RTTN-related_disorder|not_specified|not_provided|Microcephalic_primordial_dwarfism_due_to_RTTN_deficiency": 1,
    "Methemoglobinemia_type_4": 3,
    "CYB5A-related_disorder": 1,
    "not_provided|CYB5A-related_disorder": 1,
    "CNDP1-related_disorder": 1,
    "ZNF407-related_disorder": 25,
    "ZNF407-related_disorder|not_provided|not_specified": 2,
    "ZNF407-related_disorder|not_specified|not_provided": 5,
    "not_specified|ZNF407-related_disorder": 2,
    "not_specified|ZNF407-related_disorder|not_provided": 3,
    "not_specified|not_provided|ZNF407-related_disorder": 2,
    "not_provided|ZNF407-related_disorder": 8,
    "not_specified|Short_stature|_impaired_intellectual_development|_microcephaly|_hypotonia|_and_ocular_anomalies": 2,
    "Short_stature|_impaired_intellectual_development|_microcephaly|_hypotonia|_and_ocular_anomalies|not_specified": 2,
    "not_provided|not_specified|ZNF407-related_disorder": 3,
    "Short_stature|_impaired_intellectual_development|_microcephaly|_hypotonia|_and_ocular_anomalies|Neurodevelopmental_delay": 1,
    "Short_stature|_impaired_intellectual_development|_microcephaly|_hypotonia|_and_ocular_anomalies": 3,
    "Radioulnar_synostosis-microcephaly-scoliosis_syndrome": 1,
    "ZNF407-related_disorder|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|ZNF407-related_disorder": 1,
    "Aural_atresia|_congenital": 25,
    "not_provided|Aural_atresia|_congenital": 1,
    "Aural_atresia|_congenital|not_provided": 3,
    "TSHZ1-related_disorder": 31,
    "not_specified|TSHZ1-related_disorder": 7,
    "TSHZ1-related_disorder|not_specified": 6,
    "not_provided|TSHZ1-related_disorder": 3,
    "not_specified|not_provided|TSHZ1-related_disorder|Aural_atresia|_congenital": 1,
    "not_specified|not_provided|Aural_atresia|_congenital": 3,
    "TSHZ1-related_disorder|not_provided|not_specified": 1,
    "not_specified|Aural_atresia|_congenital": 1,
    "TSHZ1-related_disorder|not_provided": 3,
    "not_specified|GALR1-related_disorder": 1,
    "NFATC1-related_disorder": 12,
    "not_provided|NFATC1-related_disorder": 20,
    "NFATC1-related_disorder|not_provided": 12,
    "not_specified|NFATC1-related_disorder": 1,
    "CTDP1-related_disorder": 9,
    "Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome|not_provided|not_specified": 2,
    "not_provided|Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome": 6,
    "not_provided|CTDP1-related_disorder": 10,
    "CTDP1-related_disorder|not_provided": 12,
    "not_specified|not_provided|Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome": 3,
    "not_specified|Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome|not_provided": 1,
    "Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome": 1,
    "Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome|not_provided": 2,
    "not_specified|CTDP1-related_disorder|not_provided": 1,
    "CTDP1-related_disorder|not_specified": 1,
    "not_specified|not_provided|CTDP1-related_disorder": 2,
    "not_specified|CTDP1-related_disorder": 1,
    "not_provided|not_specified|CTDP1-related_disorder": 1,
    "not_provided|Congenital_cataracts-facial_dysmorphism-neuropathy_syndrome|not_specified": 1,
    "Choanal_atresia-hearing_loss-cardiac_defects-craniofacial_dysmorphism_syndrome|not_provided": 2,
    "TXNL4A-related_disorder|Choanal_atresia-hearing_loss-cardiac_defects-craniofacial_dysmorphism_syndrome": 2,
    "Choanal_atresia-hearing_loss-cardiac_defects-craniofacial_dysmorphism_syndrome": 10,
    "Choanal_atresia-hearing_loss-cardiac_defects-craniofacial_dysmorphism_syndrome|Inborn_genetic_diseases": 1,
    "TXNL4A-related_disorder": 3,
    "not_provided|TXNL4A-related_disorder": 1,
    "not_provided|Choanal_atresia-hearing_loss-cardiac_defects-craniofacial_dysmorphism_syndrome": 1,
    "TXNL4A-related_disorder|not_provided": 1,
    "PLPP2-related_disorder": 1,
    "PLPP2-related_disorder|not_specified": 1,
    "BSG-related_disorder": 12,
    "BLOOD_GROUP--OK": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_17": 18,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_17|not_provided": 1,
    "Febrile_seizures|_familial|_2": 7,
    "HCN2_related_developmental_and_epileptic_encephalopathy": 8,
    "HCN2-related_disorder": 18,
    "not_provided|HCN2_related_developmental_and_epileptic_encephalopathy": 3,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_17|HCN2_related_developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|HCN2-related_disorder": 2,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_17|Inborn_genetic_diseases": 2,
    "Generalized_epilepsy|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)": 1,
    "not_provided|HCN2_related_developmental_and_epileptic_encephalopathy|Neurodevelopmental_delay": 1,
    "HCN2-related_disorder|not_specified": 1,
    "Febrile_seizures|_familial|_2|Epilepsy|_idiopathic_generalized|_susceptibility_to|_17": 1,
    "HCN2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Febrile_seizures|_familial|_2": 1,
    "Inborn_genetic_diseases|Epilepsy|_idiopathic_generalized|_susceptibility_to|_17": 1,
    "HCN2-associated_Epilepsy_syndrome": 1,
    "POLRMT-related_disorder": 11,
    "Combined_oxidative_phosphorylation_deficiency_55": 31,
    "not_specified|Combined_oxidative_phosphorylation_deficiency_55": 7,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_55": 4,
    "Combined_oxidative_phosphorylation_deficiency_55|not_specified": 5,
    "not_specified|POLRMT-related_disorder": 1,
    "Progressive_sclerosing_poliodystrophy|Autosomal_dominant_progressive_external_ophthalmoplegia": 1,
    "POLRMT-related_disorder|not_provided|Combined_oxidative_phosphorylation_deficiency_55": 1,
    "Combined_oxidative_phosphorylation_deficiency_55|not_provided": 1,
    "not_specified|POLRMT-related_disorder|not_provided": 1,
    "not_provided|not_specified|atypical_cerebral_palsy": 1,
    "not_provided|atypical_cerebral_palsy": 1,
    "ELANE-related_disorder": 8,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 142,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_specified|not_provided": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant": 27,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_provided": 7,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases": 27,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 81,
    "Inborn_genetic_diseases|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 23,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided": 2,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided": 12,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 3,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases": 26,
    "not_specified|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 1,
    "Inborn_genetic_diseases|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 18,
    "ELANE-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases": 3,
    "not_specified|not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 2,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 4,
    "not_provided|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 6,
    "Autoinflammatory_syndrome|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|ELANE-related_disorder": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Cyclical_neutropenia": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ELANE-related_disorder|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases": 3,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Autoinflammatory_syndrome": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases|not_provided": 3,
    "ELANE-related_disorder|Autoinflammatory_syndrome|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 2,
    "Inborn_genetic_diseases|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_provided": 1,
    "ELANE-related_disorder|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Autoinflammatory_syndrome|not_provided": 1,
    "Cyclical_neutropenia": 10,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_specified": 3,
    "ELANE-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 1,
    "not_provided|Inborn_genetic_diseases|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 1,
    "not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_specified|ELANE-related_disorder": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified|not_provided": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|ELANE-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|ELANE-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ELANE-related_disorder|not_specified|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases|not_specified": 2,
    "ELANE-related_disorder|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified": 1,
    "Inborn_genetic_diseases|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|ELANE-related_disorder": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_specified|not_provided|Autoinflammatory_syndrome": 1,
    "not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 6,
    "ELANE-related_disorder|not_provided|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases|Cyclical_neutropenia": 1,
    "Autoinflammatory_syndrome|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_provided": 1,
    "Autoinflammatory_syndrome|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|ELANE-related_disorder": 1,
    "Autoinflammatory_syndrome|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_specified": 1,
    "ELANE-related_disorder|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 2,
    "Inborn_genetic_diseases|not_specified|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 1,
    "Inborn_genetic_diseases|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified|not_provided": 2,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Autoinflammatory_syndrome|not_provided|ELANE-related_disorder": 1,
    "Autoinflammatory_syndrome|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Inborn_genetic_diseases": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified|ELANE-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Autoinflammatory_syndrome": 1,
    "not_specified|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_provided": 1,
    "not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|Autoinflammatory_syndrome|not_specified": 1,
    "not_specified|not_provided|ELANE-related_disorder|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|ELANE-related_disorder": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Decreased_total_neutrophil_count": 1,
    "Autoinflammatory_syndrome|not_provided|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 2,
    "X-linked_severe_congenital_neutropenia|not_provided": 2,
    "not_provided|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|ELANE-related_disorder": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Autoinflammatory_syndrome|not_provided": 1,
    "Autosomal_dominant_severe_congenital_neutropenia": 1,
    "Autoinflammatory_syndrome|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Inborn_genetic_diseases|ELANE-related_disorder|not_provided": 1,
    "not_specified|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Autoinflammatory_syndrome|ELANE-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Cyclical_neutropenia|not_specified": 1,
    "Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Autoinflammatory_syndrome|not_specified": 1,
    "ELANE-related_disorder|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "ELANE-related_disorder|Inborn_genetic_diseases|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant": 1,
    "not_specified|Cyclical_neutropenia|Neutropenia|_severe_congenital|_1|_autosomal_dominant|not_provided|Autoinflammatory_syndrome": 1,
    "CFD-related_disorder": 1,
    "Recurrent_Neisseria_infections_due_to_factor_D_deficiency|not_provided": 3,
    "Recurrent_Neisseria_infections_due_to_factor_D_deficiency": 5,
    "CFD-related_disorder|not_provided": 2,
    "not_provided|Recurrent_Neisseria_infections_due_to_factor_D_deficiency": 1,
    "not_specified|CFD-related_disorder|not_provided": 1,
    "not_provided|CFD-related_disorder": 2,
    "GUILLOUET-GORDON_SYNDROME": 14,
    "not_specified|GUILLOUET-GORDON_SYNDROME": 2,
    "KISS1R-related_disorder": 4,
    "KISS1R-related_disorder|not_provided": 4,
    "KISS1R-related_disorder|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|Central_precocious_puberty_1|not_provided": 1,
    "not_provided|not_specified|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_8_with_or_without_anosmia": 4,
    "Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|Central_precocious_puberty_1": 1,
    "not_provided|Hypogonadotropic_hypogonadism_8_without_anosmia|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|Central_precocious_puberty_1": 1,
    "Inborn_genetic_diseases|Central_precocious_puberty_1": 1,
    "Hypogonadotropic_hypogonadism_8_without_anosmia": 3,
    "Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|not_provided": 1,
    "not_specified|not_provided|KISS1R-related_disorder": 1,
    "Bilateral_cryptorchidism|Microphallus|not_provided|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|Central_precocious_puberty_1": 1,
    "not_provided|Hypogonadotropic_hypogonadism_8_without_anosmia": 1,
    "not_provided|Abnormality_of_the_genitourinary_system": 1,
    "not_provided|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|not_specified|Central_precocious_puberty_1": 1,
    "Central_precocious_puberty_1|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|not_provided|not_specified": 1,
    "not_provided|Hypogonadotropic_hypogonadism_8_with_or_without_anosmia|Central_precocious_puberty_1": 1,
    "KISS1R-related_disorder|Hypogonadotropic_hypogonadism_8_without_anosmia|not_provided|Hypogonadotropic_hypogonadism": 1,
    "ABCA7-related_disorder": 30,
    "ABCA7-related_disorder|not_provided": 6,
    "not_provided|Alzheimer_disease_9": 1,
    "not_provided|Neuromuscular_disease|not_specified": 1,
    "not_provided|ABCA7-related_disorder": 7,
    "ABCA7-related_disorder|Primary_degenerative_dementia_of_the_Alzheimer_type|_presenile_onset|not_specified|not_provided|Alzheimer_disease_9": 1,
    "ABCA7-related_disorder|not_specified": 1,
    "Alzheimer_disease_9|not_specified": 3,
    "Flexion_contracture|not_provided": 3,
    "Alzheimer_disease_9|not_specified|not_provided": 1,
    "not_provided|Alzheimer_disease_9|ABCA7-related_disorder": 1,
    "Alzheimer_disease_9|not_provided": 1,
    "ABCA7-related_disorder|not_provided|not_specified|Alzheimer_disease_9": 1,
    "GPX4-related_disorder": 2,
    "not_provided|GPX4-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Spondylometaphyseal_dysplasia|_Sedaghatian_type": 1,
    "Spondylometaphyseal_dysplasia|_Sedaghatian_type": 4,
    "not_provided|Spondylometaphyseal_dysplasia|_Sedaghatian_type": 2,
    "Spondylometaphyseal_dysplasia|_Sedaghatian_type|not_provided": 1,
    "Spondylometaphyseal_dysplasia|_Sedaghatian_type|not_provided|GPX4-related_disorder": 1,
    "Peutz-Jeghers_syndrome": 903,
    "Peutz-Jeghers_syndrome|not_provided": 5,
    "not_provided|Peutz-Jeghers_syndrome": 24,
    "not_specified|Peutz-Jeghers_syndrome": 21,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome": 62,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 501,
    "not_provided|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 183,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 14,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 19,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 5,
    "Peutz-Jeghers_syndrome|Germ_cell_tumor_of_testis|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 9,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Carcinoma_of_pancreas|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 6,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 98,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|See_cases": 1,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 9,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 3,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Germ_cell_tumor_of_testis|Familial_pancreatic_carcinoma": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 14,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 13,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 4,
    "Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome": 8,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 19,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome": 5,
    "Familial_pancreatic_carcinoma|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|not_provided": 13,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 3,
    "not_specified|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 7,
    "Peutz-Jeghers_syndrome|Germ_cell_tumor_of_testis|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 34,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 5,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|STK11-related_disorder": 2,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 2,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Squamous_cell_lung_carcinoma|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Peutz-Jeghers_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|not_specified": 3,
    "Peutz-Jeghers_syndrome|not_specified": 4,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_pancreatic_carcinoma|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 16,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Peutz-Jeghers_syndrome": 4,
    "STK11-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Peutz-Jeghers_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 5,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 11,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "Hereditary_cancer-predisposing_syndrome|STK11-related_disorder|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 2,
    "Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 3,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|not_provided|Carcinoma_of_pancreas": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Peutz-Jeghers_syndrome": 5,
    "Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome|Squamous_cell_lung_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Squamous_cell_lung_carcinoma|Peutz-Jeghers_syndrome": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 2,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Germ_cell_tumor_of_testis|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hepatoblastoma|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|Marfanoid_habitus_and_intellectual_disability": 1,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 3,
    "Familial_ovarian_cancer|STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 1,
    "Malignant_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "STK11-related_disorder|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 2,
    "STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "STK11-related_disorder": 1,
    "STK11-related_disorder|Germ_cell_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "not_specified|not_provided|Squamous_cell_lung_carcinoma": 1,
    "Squamous_cell_lung_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Carcinoma_of_colon": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|not_specified|Carcinoma_of_colon": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Carcinoma_of_pancreas|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_testis": 1,
    "Familial_ovarian_cancer|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Peutz-Jeghers_syndrome": 1,
    "Arthrogryposis|_distal|_with_impaired_proprioception_and_touch|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Carcinoma_of_pancreas|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Malignant_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|Peutz-Jeghers_syndrome": 1,
    "Germ_cell_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 2,
    "STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Endometrial_carcinoma": 1,
    "Peutz-Jeghers_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Peutz-Jeghers_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 2,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 3,
    "Breast_and/or_ovarian_cancer|Malignant_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Carcinoma_of_pancreas|Peutz-Jeghers_syndrome": 1,
    "Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Bile_duct_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 3,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma": 1,
    "Malignant_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "not_provided|Peutz-Jeghers_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 2,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Peutz-Jeghers_syndrome|Pigmentary_skin_disorders": 1,
    "Carcinoma_of_colon|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|STK11-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome": 2,
    "Peutz-Jeghers_syndrome|not_specified|not_provided": 1,
    "Peutz-Jeghers_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Familial_pancreatic_carcinoma|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Carcinoma_of_pancreas|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_provided|Multiple_endocrine_neoplasia|_type_1": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 1,
    "Germ_cell_tumor_of_testis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Peutz-Jeghers_syndrome": 1,
    "not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Germ_cell_tumor_of_testis|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma": 1,
    "Familial_ovarian_cancer|Melanoma|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Periorbital_hyperpigmentation|Intestinal_polyposis": 1,
    "not_specified|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "STK11-related_disorder|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Carcinoma_of_pancreas": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome": 2,
    "Peutz-Jeghers_syndrome|Familial_ovarian_cancer": 2,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Peutz-Jeghers_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "STK11-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Peutz-Jeghers_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "STK11-related_disorder|Malignant_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Generalized_juvenile_polyposis/juvenile_polyposis_coli|Familial_adenomatous_polyposis_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|Peutz-Jeghers_syndrome": 1,
    "Familial_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Carcinoma_of_colon": 1,
    "B_Lymphoblastic_Leukemia/Lymphoma|_Not_Otherwise_Specified|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|not_provided": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome|Carcinoma_of_pancreas|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Lip_and_oral_cavity_carcinoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|STK11-related_disorder": 1,
    "Gastric_cancer|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Peutz-Jeghers_syndrome": 1,
    "Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Germ_cell_tumor_of_testis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|not_specified|not_provided": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|See_cases": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Generalized_juvenile_polyposis/juvenile_polyposis_coli": 1,
    "Hereditary_cancer-predisposing_syndrome|Ovarian_cancer|not_specified|not_provided|Peutz-Jeghers_syndrome": 2,
    "Peutz-Jeghers_syndrome|Childhood_neoplasm|Hereditary_cancer-predisposing_syndrome": 1,
    "Germ_cell_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Embryonal_rhabdomyosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Peutz-Jeghers_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Germ_cell_tumor_of_testis|Carcinoma_of_pancreas|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Peutz-Jeghers_syndrome|Breast_carcinoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|Carcinoma_of_pancreas|Malignant_tumor_of_testis|not_provided": 1,
    "Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Peutz-Jeghers_syndrome": 1,
    "STK11-related_disorder|Germ_cell_tumor_of_testis|Peutz-Jeghers_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_pancreas|Breast_carcinoma": 1,
    "STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Peutz-Jeghers_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 1,
    "not_specified|Peutz-Jeghers_syndrome|Hereditary_cancer-predisposing_syndrome|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "not_provided|STK11-related_disorder|Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|STK11-related_disorder": 1,
    "Malignant_tumor_of_testis|Peutz-Jeghers_syndrome|Carcinoma_of_pancreas|Hereditary_cancer-predisposing_syndrome|not_provided|Melanoma|_cutaneous_malignant|_susceptibility_to|_1": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Peutz-Jeghers_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|Germ_cell_tumor_of_testis|Melanoma|_cutaneous_malignant|_susceptibility_to|_1|Familial_pancreatic_carcinoma": 1,
    "Peutz-Jeghers_syndrome|Familial_pancreatic_carcinoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Peutz-Jeghers_syndrome|Malignant_neoplasm_of_brain|Malignant_tumor_of_breast": 1,
    "ATP5F1D-related_disorder": 4,
    "not_provided|ATP5F1D-related_disorder|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_5": 1,
    "not_provided|ATP5F1D-related_disorder": 4,
    "ATP5F1D-related_disorder|not_provided": 3,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_5|Decreased_activity_of_mitochondrial_ATP_synthase_complex": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_5|Mitochondrial_disease": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_5": 1,
    "ATP5F1D-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "MIDN-related_disorder": 3,
    "Leigh_syndrome|Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3|Leigh_syndrome": 1,
    "not_provided|NDUFS7-related_disorder": 2,
    "not_specified|NDUFS7-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3|not_provided|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3|not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_1": 1,
    "not_provided|NDUFS7-related_disorder|not_specified": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_3": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3|Inborn_genetic_diseases": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3": 6,
    "Exertional_Heat_Illness": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_3|not_provided": 2,
    "NDUFS7-related_disorder": 5,
    "NDUFS7-related_disorder|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Leigh_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|Leigh_syndrome": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Leigh_syndrome": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|Deficiency_of_guanidinoacetate_methyltransferase|Leigh_syndrome": 3,
    "Deficiency_of_guanidinoacetate_methyltransferase": 68,
    "not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Mitochondrial_complex_I_deficiency|Leigh_syndrome": 1,
    "not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 4,
    "Deficiency_of_guanidinoacetate_methyltransferase|not_provided": 4,
    "not_specified|Deficiency_of_guanidinoacetate_methyltransferase|not_provided": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 10,
    "Cerebral_creatine_deficiency_syndrome|Inborn_genetic_diseases|Deficiency_of_guanidinoacetate_methyltransferase": 4,
    "Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome": 32,
    "Cerebral_creatine_deficiency_syndrome": 298,
    "not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome": 7,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome": 11,
    "Cerebral_creatine_deficiency_syndrome|not_provided": 8,
    "Cerebral_creatine_deficiency_syndrome|Inborn_genetic_diseases": 5,
    "Cerebral_creatine_deficiency_syndrome|not_provided|not_specified": 1,
    "GAMT-related_disorder|Cerebral_creatine_deficiency_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Leigh_syndrome": 1,
    "Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 43,
    "Cerebral_creatine_deficiency_syndrome|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 7,
    "Cerebral_creatine_deficiency_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Cerebral_creatine_deficiency_syndrome": 1,
    "GAMT-related_disorder|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|not_specified": 1,
    "Cerebral_creatine_deficiency_syndrome|Inborn_genetic_diseases|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 3,
    "Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "not_specified|Cerebral_creatine_deficiency_syndrome": 5,
    "GAMT-related_disorder|not_provided": 1,
    "GAMT-related_disorder": 2,
    "not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|GAMT-related_disorder": 1,
    "GAMT-related_disorder|not_specified|not_provided": 1,
    "Cerebral_creatine_deficiency_syndrome|GAMT-related_disorder|not_provided|Inborn_genetic_diseases|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 3,
    "Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome|not_provided|GAMT-related_disorder": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome|not_specified": 4,
    "Deficiency_of_guanidinoacetate_methyltransferase|not_provided|Cerebral_creatine_deficiency_syndrome": 1,
    "not_specified|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 2,
    "Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome": 2,
    "not_provided|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 7,
    "not_specified|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase|not_provided": 1,
    "Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase|not_specified": 3,
    "not_provided|not_specified|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome": 1,
    "not_provided|Deficiency_of_guanidinoacetate_methyltransferase|not_specified": 1,
    "Cerebral_creatine_deficiency_syndrome|not_specified": 7,
    "not_provided|Cerebral_creatine_deficiency_syndrome": 5,
    "GAMT-related_disorder|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase|not_provided": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome": 5,
    "Deficiency_of_guanidinoacetate_methyltransferase|Intellectual_disability|Cerebral_creatine_deficiency_syndrome": 1,
    "Cerebral_creatine_deficiency_syndrome|GAMT-related_disorder": 1,
    "Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Inborn_genetic_diseases|not_provided|Cerebral_creatine_deficiency_syndrome": 1,
    "Cerebral_creatine_deficiency_syndrome|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|not_specified": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|not_provided|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified": 1,
    "not_specified|Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|GAMT-related_disorder": 1,
    "not_provided|Cerebral_creatine_deficiency_syndrome|Inborn_genetic_diseases": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|not_specified|not_provided|Cerebral_creatine_deficiency_syndrome": 1,
    "Cerebral_creatine_deficiency_syndrome|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases": 1,
    "not_provided|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase|Abnormality_of_the_nervous_system": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified": 1,
    "not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome|Inborn_genetic_diseases": 2,
    "Cerebral_creatine_deficiency_syndrome|not_provided|Inborn_genetic_diseases|Deficiency_of_guanidinoacetate_methyltransferase": 2,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 2,
    "Cerebral_creatine_deficiency_syndrome|not_specified|GAMT-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Cerebral_creatine_deficiency_syndrome|not_provided|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Cerebral_creatine_deficiency_syndrome|Inborn_genetic_diseases|Deficiency_of_guanidinoacetate_methyltransferase|not_provided": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Inborn_genetic_diseases|GAMT-related_disorder|not_provided|Cerebral_creatine_deficiency_syndrome": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_specified": 1,
    "Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases": 1,
    "GAMT-related_disorder|Deficiency_of_guanidinoacetate_methyltransferase|Cerebral_creatine_deficiency_syndrome": 2,
    "Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase|not_provided": 1,
    "Inborn_genetic_diseases|GAMT-related_disorder|Guanidinoacetate_methyltransferase_(GAMT)_deficiency|Cerebral_creatine_deficiency_syndrome|not_specified|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|Intellectual_disability": 1,
    "Deficiency_of_guanidinoacetate_methyltransferase|Inborn_genetic_diseases|not_provided|Cerebral_creatine_deficiency_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Inborn_genetic_diseases|Cerebral_creatine_deficiency_syndrome|not_provided|Deficiency_of_guanidinoacetate_methyltransferase|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|GAMT-related_disorder|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "Inborn_genetic_diseases|GAMT-related_disorder|not_provided|Cerebral_creatine_deficiency_syndrome|Deficiency_of_guanidinoacetate_methyltransferase": 1,
    "RPS15-related_disorder|not_specified|not_provided": 1,
    "RPS15-related_disorder": 2,
    "not_provided|APC2-related_disorder": 23,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10": 12,
    "Inborn_genetic_diseases|not_provided|APC2-related_disorder": 3,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_recessive_74": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_74": 13,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Intellectual_developmental_disorder|_autosomal_recessive_74|not_provided": 1,
    "APC2-related_disorder|not_specified|not_provided": 1,
    "APC2-related_disorder": 20,
    "APC2-related_disorder|not_provided": 9,
    "not_specified|Intellectual_developmental_disorder|_autosomal_recessive_74": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_recessive_74|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_74": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_74|Inborn_genetic_diseases": 1,
    "See_cases|not_provided|Intellectual_developmental_disorder|_autosomal_recessive_74": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Inborn_genetic_diseases": 2,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Intellectual_developmental_disorder|_autosomal_recessive_74|Inborn_genetic_diseases": 2,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Intellectual_developmental_disorder|_autosomal_recessive_74": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_74|Cortical_dysplasia|_complex|_with_other_brain_malformations_10": 1,
    "APC2-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_74|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|APC2-related_disorder|not_specified|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_74|Cortical_dysplasia|_complex|_with_other_brain_malformations_10|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|APC2-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_developmental_disorder|_autosomal_recessive_74|Cortical_dysplasia|_complex|_with_other_brain_malformations_10": 1,
    "not_provided|Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Intellectual_developmental_disorder|_autosomal_recessive_74": 1,
    "Inborn_genetic_diseases|APC2-related_disorder|not_provided": 1,
    "Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Intellectual_developmental_disorder|_autosomal_recessive_74|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Cortical_dysplasia|_complex|_with_other_brain_malformations_10": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_74|not_specified|not_provided|Inborn_genetic_diseases|Cortical_dysplasia|_complex|_with_other_brain_malformations_10": 1,
    "not_provided|Inborn_genetic_diseases|APC2-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_74|Cortical_dysplasia|_complex|_with_other_brain_malformations_10|Inborn_genetic_diseases": 1,
    "REEP6-related_disorder": 2,
    "not_provided|Retinitis_pigmentosa_77": 6,
    "not_provided|REEP6-related_disorder": 3,
    "REEP6-related_disorder|not_provided": 4,
    "Retinitis_pigmentosa_77|not_provided": 7,
    "Retinitis_pigmentosa_77": 6,
    "not_provided|Retinal_dystrophy|REEP6-related_disorder": 1,
    "TCF3-related_disorder": 6,
    "Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|TCF3-related_disorder": 1,
    "Agammaglobulinemia_8|_autosomal_dominant": 8,
    "TCF3-related_disorder|not_provided": 24,
    "Agammaglobulinemia_8b|_autosomal_recessive|Agammaglobulinemia_8|_autosomal_dominant": 2,
    "not_provided|Agammaglobulinemia_8b|_autosomal_recessive|Agammaglobulinemia_8|_autosomal_dominant": 2,
    "Inborn_genetic_diseases|Agammaglobulinemia_8|_autosomal_dominant|not_provided": 1,
    "Agammaglobulinemia_8b|_autosomal_recessive": 3,
    "not_provided|TCF3-related_disorder": 15,
    "Agammaglobulinemia_8|_autosomal_dominant|not_provided": 3,
    "Agammaglobulinemia_8b|_autosomal_recessive|Agammaglobulinemia_8|_autosomal_dominant|not_provided": 4,
    "Inborn_genetic_diseases|Agammaglobulinemia_8|_autosomal_dominant": 1,
    "not_provided|Agammaglobulinemia_8b|_autosomal_recessive": 2,
    "Agammaglobulinemia_8b|_autosomal_recessive|not_provided": 1,
    "Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive|TCF3-related_disorder|not_provided": 1,
    "not_provided|Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive": 2,
    "Myeloproliferative_neoplasm|_unclassifiable|not_specified|not_provided": 1,
    "Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive|not_provided": 2,
    "Myeloproliferative_neoplasm|_unclassifiable|not_provided": 1,
    "not_provided|Myeloproliferative_neoplasm|_unclassifiable": 2,
    "not_provided|Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_provided|Agammaglobulinemia_8|_autosomal_dominant": 5,
    "TCF3-related_disorder|not_provided|Agammaglobulinemia_8|_autosomal_dominant": 1,
    "Inborn_genetic_diseases|not_provided|Agammaglobulinemia_8b|_autosomal_recessive": 1,
    "Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive": 3,
    "not_provided|Inborn_genetic_diseases|TCF3-related_disorder": 2,
    "Myeloproliferative_neoplasm|_unclassifiable|Agammaglobulinemia_8|_autosomal_dominant": 1,
    "not_provided|TCF3-related_disorder|Inborn_genetic_diseases": 1,
    "TCF3-related_disorder|not_provided|Agammaglobulinemia_8b|_autosomal_recessive|Agammaglobulinemia_8|_autosomal_dominant": 1,
    "Agammaglobulinemia_8b|_autosomal_recessive|Agammaglobulinemia_8|_autosomal_dominant|not_provided|TCF3-related_disorder": 1,
    "Agammaglobulinemia_8b|_autosomal_recessive|Agammaglobulinemia_8|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "Agammaglobulinemia_8|_autosomal_dominant|not_specified|not_provided": 1,
    "Agammaglobulinemia_8|_autosomal_dominant|Agammaglobulinemia_8b|_autosomal_recessive|not_provided|TCF3-related_disorder": 1,
    "Intellectual_disability-strabismus_syndrome|not_provided": 2,
    "Intellectual_disability-strabismus_syndrome": 18,
    "Intellectual_disability-strabismus_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "ADAT3-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|not_specified|ADAT3-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_brain_abnormalities|Intellectual_disability-strabismus_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability-strabismus_syndrome|not_specified|not_provided": 1,
    "ADAT3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Intellectual_disability-strabismus_syndrome": 2,
    "Intellectual_disability-strabismus_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability-strabismus_syndrome|Inborn_genetic_diseases|Intellectual_disability": 1,
    "ADAT3-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability-strabismus_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability-strabismus_syndrome": 1,
    "ADAT3-related_disorder": 1,
    "not_provided|not_specified|ADAT3-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|BTBD2-related_disorder": 1,
    "BTBD2-related_disorder": 1,
    "not_provided|Hermansky-Pudlak_syndrome_10|AP3D1-related_disorder": 1,
    "AP3D1-related_disorder|not_provided": 22,
    "Hermansky-Pudlak_syndrome_10": 5,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_10|not_provided": 1,
    "not_provided|AP3D1-related_disorder": 10,
    "AP3D1-related_disorder": 6,
    "not_provided|Inborn_genetic_diseases|AP3D1-related_disorder": 1,
    "AP3D1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome_10|not_provided": 3,
    "Hermansky-Pudlak_syndrome_10|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Hermansky-Pudlak_syndrome_10": 3,
    "Inborn_genetic_diseases|not_provided|AP3D1-related_disorder": 1,
    "not_provided|AP3D1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_10|Abnormal_bleeding|Thrombocytopenia": 1,
    "not_specified|not_provided|AP3D1-related_disorder": 1,
    "NIL-DESHWAR_NEURODEVELOPMENTAL_SYNDROME": 6,
    "DOT1L-related_condition|NIL-DESHWAR_NEURODEVELOPMENTAL_SYNDROME": 1,
    "AMH-related_disorder": 3,
    "AMH-related_disorder|not_provided": 2,
    "not_provided|AMH-related_disorder": 3,
    "Oromandibular-limb_hypogenesis_spectrum|not_provided|not_specified": 1,
    "Persistent_mullerian_duct_syndrome|_type_I|not_provided": 1,
    "Persistent_Mullerian_duct_syndrome|Persistent_mullerian_duct_syndrome|_type_I": 1,
    "not_provided|Inborn_genetic_diseases|Persistent_Mullerian_duct_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|AMH-related_disorder": 1,
    "not_provided|not_specified|Persistent_Mullerian_duct_syndrome": 1,
    "Persistent_mullerian_duct_syndrome|_type_I": 2,
    "not_specified|Persistent_Mullerian_duct_syndrome|not_provided": 1,
    "Joubert_syndrome_36|In_utero_death": 1,
    "Leukodystrophy|LEUKODYSTROPHY_AND_CEREBELLAR_ATROPHY": 1,
    "Global_developmental_delay|not_specified": 1,
    "LMNB2-related_disorder": 5,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9": 214,
    "not_specified|Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9": 13,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 228,
    "Progressive_myoclonic_epilepsy_type_9|LMNB2-related_disorder|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "not_provided|not_specified|Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9": 3,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|LMNB2-related_disorder": 1,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|not_provided": 6,
    "Progressive_myoclonic_epilepsy_type_9|Microcephaly_27|_primary|_autosomal_dominant|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_specified|not_provided": 3,
    "not_specified|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 8,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_specified|LMNB2-related_disorder": 1,
    "not_provided|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 3,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|not_specified|not_provided": 2,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_specified": 16,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|not_specified": 16,
    "LMNB2-related_disorder|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 2,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|Microcephaly_27|_primary|_autosomal_dominant": 2,
    "not_provided|Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9": 5,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_provided": 11,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_provided|not_specified": 2,
    "LMNB2-related_disorder|Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9": 2,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_provided|Acquired_partial_lipodystrophy": 1,
    "LMNB2-related_disorder|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|not_provided": 1,
    "LMNB2-related_disorder|See_cases|Microcephaly_27|_primary|_autosomal_dominant": 1,
    "Microcephaly_27|_primary|_autosomal_dominant|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "Microcephaly_27|_primary|_autosomal_dominant": 4,
    "Microcephaly_27|_primary|_autosomal_dominant|not_specified": 1,
    "not_specified|not_provided|LMNB2-related_disorder|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "Microcephaly_27|_primary|_autosomal_dominant|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to|Microcephaly_27|_primary|_autosomal_dominant|Progressive_myoclonic_epilepsy_type_9|not_specified|not_provided|Acquired_partial_lipodystrophy": 1,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|LMNB2-related_disorder": 2,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|Microcephaly_27|_primary|_autosomal_dominant|not_specified|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|Generalized_myoclonic_seizure": 1,
    "Progressive_myoclonic_epilepsy_type_9": 1,
    "LMNB2-related_disorder|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|not_specified|not_provided": 1,
    "Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "LMNB2-related_disorder|not_provided|not_specified|Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to": 1,
    "Progressive_myoclonic_epilepsy_type_9|Lipodystrophy|_partial|_acquired|_susceptibility_to|not_provided|Acquired_partial_lipodystrophy": 1,
    "not_provided|Lipodystrophy|_partial|_acquired|_susceptibility_to|Progressive_myoclonic_epilepsy_type_9|not_specified": 1,
    "THOP1-related_disorder": 1,
    "TLE6-related_disorder": 12,
    "Preimplantation_embryonic_lethality_1": 4,
    "not_provided|Preimplantation_embryonic_lethality_1": 1,
    "not_provided|TLE6-related_disorder": 1,
    "GNA11-related_disorder|not_provided": 2,
    "Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2": 17,
    "Familial_hypocalciuric_hypercalcemia_2": 3,
    "GNA11-related_disorder": 4,
    "Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2|not_provided": 10,
    "Autosomal_dominant_hypocalcemia_2|not_provided|Familial_hypocalciuric_hypercalcemia_2": 1,
    "Autosomal_dominant_hypocalcemia_2|not_provided": 2,
    "Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2|GNA11-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2": 1,
    "Autosomal_dominant_hypocalcemia_2|Familial_hypocalciuric_hypercalcemia_2|not_provided": 3,
    "not_provided|Autosomal_dominant_hypocalcemia_2|Familial_hypocalciuric_hypercalcemia_2": 6,
    "not_provided|Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2|GNA11-related_disorder": 1,
    "not_provided|Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2": 6,
    "not_provided|GNA11-related_disorder": 2,
    "Lobular_capillary_hemangiomas|CLOVES_syndrome|not_provided|Capillary_malformation|Segmental_undergrowth_associated_with_capillary_malformation": 1,
    "Autosomal_dominant_hypocalcemia_2": 2,
    "Autosomal_dominant_hypocalcemia_2|Familial_hypocalciuric_hypercalcemia_2|GNA11-related_disorder|not_specified|not_provided": 1,
    "not_provided|GNA11-related_disorder|Familial_hypocalciuric_hypercalcemia_2|Autosomal_dominant_hypocalcemia_2": 1,
    "not_provided|not_specified|Autosomal_dominant_hypocalcemia_2|Familial_hypocalciuric_hypercalcemia_2": 1,
    "not_specified|not_provided|Autosomal_dominant_hypocalcemia_2|Familial_hypocalciuric_hypercalcemia_2": 1,
    "not_provided|Autosomal_dominant_hypocalcemia_2|Familial_hypocalciuric_hypercalcemia_2|not_specified": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_cerebral_atrophy|_and_visual_impairment|DOHH_related_neurodevelopmental_disorder": 4,
    "DOHH_related_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_microcephaly|_cerebral_atrophy|_and_visual_impairment": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_cerebral_atrophy|_and_visual_impairment": 4,
    "DOHH_related_neurodevelopmental_disorder": 1,
    "DOHH-related_disorder|not_specified|DOHH_related_neurodevelopmental_disorder|Neurodevelopmental_disorder_with_microcephaly|_cerebral_atrophy|_and_visual_impairment": 1,
    "FZR1-related_condition": 4,
    "Developmental_and_epileptic_encephalopathy_109": 3,
    "FZR1-related_condition|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy_109|not_provided": 1,
    "Global_developmental_delay|Autism|Seizure|Hypotonia|Cerebellar_ataxia|Developmental_and_epileptic_encephalopathy_109": 1,
    "not_provided|MFSD12_POLYMORPHISM": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_15": 19,
    "GIPC3-related_disorder|not_specified|not_provided": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_15|not_specified|not_provided": 2,
    "not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_15": 2,
    "GIPC3-related_disorder|not_provided": 1,
    "not_provided|GIPC3-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_15|not_provided": 2,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_15": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_15": 1,
    "GIPC3-related_disorder": 2,
    "not_provided|GIPC3-related_disorder": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_15|Inborn_genetic_diseases|not_specified": 1,
    "GIPC3-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_15|not_provided": 1,
    "not_provided|GIPC3-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_15|not_specified": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_15": 1,
    "TBXA2R-related_disorder|Bleeding_disorder|_platelet-type|_13|_susceptibility_to": 1,
    "TBXA2R-related_disorder": 6,
    "TBXA2R-related_disorder|not_specified": 1,
    "Bleeding_disorder|_platelet-type|_13|_susceptibility_to": 7,
    "not_provided|Bleeding_disorder|_platelet-type|_13|_susceptibility_to": 2,
    "TBXA2R-related_disorder|not_provided": 1,
    "not_provided|TBXA2R-related_disorder": 3,
    "Impaired_thromboxane_A2_agonist-induced_platelet_aggregation|not_provided|not_specified": 1,
    "Bleeding_disorder|_platelet-type|_13|_susceptibility_to|TBXA2R-related_disorder": 1,
    "not_specified|Impaired_thromboxane_A2_agonist-induced_platelet_aggregation": 1,
    "Bleeding_disorder|_platelet-type|_13|_susceptibility_to|not_provided|TBXA2R-related_disorder": 1,
    "Bleeding_disorder|_platelet-type|_13|_susceptibility_to|Asthma": 1,
    "Inborn_genetic_diseases|not_provided|Bleeding_disorder|_platelet-type|_13|_susceptibility_to": 1,
    "PIP5K1C-related_disorder": 10,
    "PIP5K1C-related_disorder|not_provided": 2,
    "not_provided|PIP5K1C-related_disorder": 2,
    "not_provided|Lethal_congenital_contracture_syndrome_3": 3,
    "Lethal_congenital_contracture_syndrome_3": 4,
    "Lethal_congenital_contracture_syndrome_3|Inborn_genetic_diseases": 1,
    "Lethal_congenital_contracture_syndrome_3|not_provided": 1,
    "PIP5K1C-related_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Novel_PIP5K1C-related_neurodevelopmental_disorder": 1,
    "PIP5K1C-related_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|Lethal_congenital_contracture_syndrome_3": 1,
    "Cone-rod_dystrophy_11|Age_related_macular_degeneration_6": 28,
    "Age_related_macular_degeneration_6|Cone-rod_dystrophy_11": 8,
    "Cone-rod_dystrophy_11|not_provided|Age_related_macular_degeneration_6": 2,
    "Cone-Rod_Dystrophy|_Dominant|Macular_degeneration": 2,
    "Age_related_macular_degeneration_6|Cone-rod_dystrophy_11|not_provided": 1,
    "Macular_degeneration|Cone-Rod_Dystrophy|_Dominant": 3,
    "Cone-rod_dystrophy_11|Age_related_macular_degeneration_6|not_provided": 10,
    "Cone-rod_dystrophy_11|Age_related_macular_degeneration_6|Retinitis_pigmentosa_95": 1,
    "not_specified|Age_related_macular_degeneration_6|Cone-rod_dystrophy_11": 1,
    "not_provided|Cone-rod_dystrophy_11|Retinal_dystrophy": 1,
    "Cone-rod_dystrophy_11|Age_related_macular_degeneration_6|not_specified": 1,
    "Cone-rod_dystrophy_11": 2,
    "Age_related_macular_degeneration_6|Cone-rod_dystrophy_11|not_provided|not_specified": 1,
    "not_provided|Cone-rod_dystrophy_11": 1,
    "Age_related_macular_degeneration_6|not_specified|not_provided|Cone-rod_dystrophy_11": 1,
    "not_specified|not_provided|Age_related_macular_degeneration_6|Cone-rod_dystrophy_11": 1,
    "RAX2-related_disorder|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_95": 1,
    "RAX2-related_disorder": 5,
    "not_provided|Cone-rod_dystrophy_11|Age_related_macular_degeneration_6": 4,
    "not_specified|not_provided|Cone-rod_dystrophy_11|Retinal_dystrophy": 1,
    "Age_related_macular_degeneration_6|not_provided": 1,
    "not_provided|Age_related_macular_degeneration_6|Retinal_dystrophy": 1,
    "Age_related_macular_degeneration_6|Cone-rod_dystrophy_11|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_95": 2,
    "not_specified|Retinitis_pigmentosa_95|not_provided": 1,
    "Retinitis_pigmentosa_95|not_specified|not_provided|Age_related_macular_degeneration_6|Cone-rod_dystrophy_11": 1,
    "Retinitis_pigmentosa_95|Retinal_dystrophy|not_provided": 1,
    "not_provided|RAX2-related_disorder": 1,
    "Retinal_dystrophy|not_specified|Cone-rod_dystrophy_11|not_provided|Age_related_macular_degeneration_6": 1,
    "not_provided|Age_related_macular_degeneration_6|Cone-rod_dystrophy_11": 2,
    "Cone-rod_dystrophy_11|Retinal_dystrophy": 1,
    "Cone-rod_dystrophy_11|Retinal_dystrophy|not_provided": 1,
    "not_specified|Cone-rod_dystrophy_11|Age_related_macular_degeneration_6|not_provided": 2,
    "not_provided|not_specified|Age_related_macular_degeneration_6|Cone-rod_dystrophy_11": 1,
    "Macular_degeneration|Cone-Rod_Dystrophy|_Dominant|not_provided": 1,
    "Cayman_type_cerebellar_ataxia": 114,
    "not_provided|Cayman_type_cerebellar_ataxia": 8,
    "Inborn_genetic_diseases|Cayman_type_cerebellar_ataxia|not_provided": 1,
    "Cayman_type_cerebellar_ataxia|not_provided": 17,
    "ATCAY-related_disorder": 2,
    "Cayman_type_cerebellar_ataxia|Inborn_genetic_diseases": 1,
    "not_provided|ATCAY-related_disorder": 2,
    "Inborn_genetic_diseases|Cayman_type_cerebellar_ataxia": 1,
    "ATCAY-related_disorder|Cayman_type_cerebellar_ataxia|not_provided": 1,
    "ATCAY-related_disorder|not_provided|Cayman_type_cerebellar_ataxia": 1,
    "not_specified|EEF2-related_disorder|not_provided": 2,
    "not_provided|EEF2-related_disorder": 2,
    "not_specified|EEF2-related_disorder": 1,
    "EEF2-related_disorder|not_specified|not_provided": 2,
    "Spinocerebellar_ataxia_type_26": 8,
    "Spinocerebellar_ataxia_type_26|not_provided": 3,
    "EEF2-related_disorder|not_provided": 5,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_26": 1,
    "EEF2-related_neurodevelopmental_disorder_with_multiple_anomalies": 1,
    "EEF2-related_disorder": 4,
    "not_provided|Spinocerebellar_ataxia_type_26": 1,
    "not_specified|not_provided|EEF2-related_disorder": 2,
    "Spinocerebellar_ataxia_type_26|not_specified|not_provided": 1,
    "Motor_delay": 1,
    "EEF2-related_Neurodevelopmental_disorder": 1,
    "PIAS4-related_disorder": 7,
    "not_specified|PIAS4-related_disorder": 1,
    "ZBTB7A-related_disorder": 4,
    "Macrocephaly|_neurodevelopmental_delay|_lymphoid_hyperplasia|_and_persistent_fetal_hemoglobin": 12,
    "not_provided|Macrocephaly|_neurodevelopmental_delay|_lymphoid_hyperplasia|_and_persistent_fetal_hemoglobin": 2,
    "Hereditary_persistence_of_fetal_hemoglobin-beta-thalassemia_syndrome|not_provided": 1,
    "Hereditary_persistence_of_fetal_hemoglobin-beta-thalassemia_syndrome": 2,
    "Cardiofaciocutaneous_syndrome_4|Cardiovascular_phenotype": 1,
    "not_specified|RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "MAP2K2-related_disorder": 5,
    "Cardiofaciocutaneous_syndrome_4|RASopathy|Cardiovascular_phenotype": 2,
    "not_provided|not_specified|Noonan_syndrome|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "not_specified|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "RASopathy|not_provided|Cardiofaciocutaneous_syndrome_4": 2,
    "Noonan_syndrome|not_specified|Cardiofaciocutaneous_syndrome_4|RASopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|MAP2K2-related_disorder|RASopathy": 1,
    "not_specified|RASopathy|Cardiofaciocutaneous_syndrome_4|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "not_specified|Cardiofaciocutaneous_syndrome_4|not_provided|RASopathy": 2,
    "Cardiofaciocutaneous_syndrome_4|not_specified|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_4": 17,
    "MAP2K2-related_disorder|RASopathy|not_provided": 1,
    "Cardiofaciocutaneous_syndrome_4|RASopathy": 5,
    "Cardiofaciocutaneous_syndrome_4|not_specified|not_provided|RASopathy|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|MAP2K2-related_disorder|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy": 1,
    "Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4": 3,
    "RASopathy|Cardiofaciocutaneous_syndrome_4|not_specified": 1,
    "MAP2K2-related_disorder|Cardiovascular_phenotype|not_specified|RASopathy|not_provided": 1,
    "RASopathy|Cardiofaciocutaneous_syndrome_4|not_provided": 2,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "Cardiofaciocutaneous_syndrome_4|RASopathy|not_specified|Noonan_syndrome|not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Cardiofaciocutaneous_syndrome_4|Cardiovascular_phenotype|RASopathy": 1,
    "MAP2K2-related_disorder|RASopathy": 2,
    "RASopathy|not_provided|not_specified|Cardiofaciocutaneous_syndrome_4": 1,
    "RASopathy|MAP2K2-related_disorder|not_provided|not_specified": 1,
    "not_specified|RASopathy|Cardio-facio-cutaneous_syndrome": 1,
    "Cardiofaciocutaneous_syndrome_4|not_specified|not_provided|RASopathy": 3,
    "MAP2K2-related_disorder|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|RASopathy|MAP2K2-related_disorder": 1,
    "RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiofaciocutaneous_syndrome_4|not_provided|RASopathy": 4,
    "Cardiovascular_phenotype|RASopathy|Cardiofaciocutaneous_syndrome_4|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_4": 1,
    "not_provided|not_specified|RASopathy|Noonan_syndrome": 1,
    "not_specified|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|not_specified|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|RASopathy|not_provided|MAP2K2-related_disorder|Noonan_syndrome": 1,
    "not_provided|Cardiofaciocutaneous_syndrome_4|RASopathy": 2,
    "not_provided|MAP2K2-related_disorder|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "RASopathy|not_specified|not_provided|MAP2K2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiofaciocutaneous_syndrome_4|not_specified|RASopathy|not_provided|MAP2K2-related_disorder": 1,
    "not_provided|RASopathy|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|not_specified": 1,
    "not_provided|RASopathy|Cardio-facio-cutaneous_syndrome|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiofaciocutaneous_syndrome_4|not_specified|MAP2K2-related_disorder|Cardiovascular_phenotype|not_provided|RASopathy": 1,
    "MAP2K2-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiofaciocutaneous_syndrome_4": 11,
    "not_provided|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome_and_Noonan-related_syndrome|RASopathy|Cardiofaciocutaneous_syndrome_4": 1,
    "not_provided|MAP2K2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "MAP2K2-related_disorder|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiofaciocutaneous_syndrome_4|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype|not_specified|Cardiofaciocutaneous_syndrome_4": 2,
    "Noonan_syndrome|Cardiovascular_phenotype|RASopathy": 1,
    "RASopathy|MAP2K2-related_disorder|not_provided|Noonan_syndrome": 1,
    "RASopathy|Cardiovascular_phenotype|not_specified|not_provided|MAP2K2-related_disorder": 1,
    "Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|not_specified|RASopathy": 1,
    "MAP2K2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|not_provided|RASopathy": 1,
    "RASopathy|not_specified|Cardiofaciocutaneous_syndrome_4|not_provided": 1,
    "MAP2K2-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_4|not_specified": 1,
    "MAP2K2-related_disorder|RASopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|not_provided|MAP2K2-related_disorder|RASopathy|Cardiofaciocutaneous_syndrome_4|Cardiovascular_phenotype": 1,
    "MAP2K2-related_disorder|Cardiofaciocutaneous_syndrome_4|not_provided|RASopathy": 1,
    "not_specified|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "Migraine|Thin_skin|High_palate|Hypotension|Malar_flattening|Abnormal_facial_shape|Short_stature|Pain|Mitral_valve_prolapse|RASopathy|MAP2K2-related_disorder": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|not_specified|RASopathy|not_provided": 1,
    "not_specified|RASopathy|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiovascular_phenotype|RASopathy|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|not_specified|Cardiofaciocutaneous_syndrome_4": 1,
    "RASopathy|MAP2K2-related_disorder|not_specified|not_provided": 1,
    "RASopathy|not_specified|not_provided|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiovascular_phenotype|RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "RASopathy|not_provided|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiovascular_phenotype|MAP2K2-related_disorder|RASopathy": 1,
    "Cardio-facio-cutaneous_syndrome|Noonan_syndrome|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|MAP2K2-related_disorder|Cardio-facio-cutaneous_syndrome|Cardiofaciocutaneous_syndrome_4|not_provided|Noonan_syndrome_1|RASopathy": 1,
    "Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|not_provided|RASopathy": 1,
    "RASopathy|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4": 1,
    "RASopathy|MAP2K2-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "MAP2K2-related_disorder|Castleman-Kojima_disease|Cardiofaciocutaneous_syndrome_4|not_provided": 1,
    "Cardio-facio-cutaneous_syndrome|Cardiofaciocutaneous_syndrome_4|not_provided|RASopathy": 2,
    "Cardio-facio-cutaneous_syndrome|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "not_specified|MAP2K2-related_disorder": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy": 1,
    "Cardiofaciocutaneous_syndrome_4|not_specified|not_provided|RASopathy|Noonan_syndrome_1": 1,
    "not_provided|RASopathy|not_specified|Cardiofaciocutaneous_syndrome_4": 1,
    "MAP2K2-related_disorder|not_provided|RASopathy|not_specified": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4|not_provided|not_specified|RASopathy": 1,
    "Cardiovascular_phenotype|not_provided|RASopathy|Neurofibromatosis-Noonan_syndrome|not_specified": 1,
    "not_specified|RASopathy|not_provided|Cardiovascular_phenotype|Cardiofaciocutaneous_syndrome_4": 1,
    "not_specified|not_provided|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "RASopathy|MAP2K2-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "MAP2K2-related_disorder|not_specified|RASopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiofaciocutaneous_syndrome_4|Cardiovascular_phenotype|RASopathy": 1,
    "not_specified|not_provided|Noonan_syndrome_with_multiple_lentigines|Noonan_syndrome_1": 1,
    "not_provided|RASopathy|Cardiofaciocutaneous_syndrome_4": 1,
    "Cardiofaciocutaneous_syndrome_4|not_provided|RASopathy|Cardiofaciocutaneous_syndrome_1": 1,
    "Cardiofaciocutaneous_syndrome_4|Cardio-facio-cutaneous_syndrome": 1,
    "RASopathy|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiofaciocutaneous_syndrome_4|not_specified|RASopathy": 1,
    "Noonan_syndrome|Cardiofaciocutaneous_syndrome_4|RASopathy": 1,
    "not_specified|RASopathy|Cardiovascular_phenotype|Noonan_syndrome": 1,
    "not_provided|Cardiofaciocutaneous_syndrome_4": 1,
    "not_provided|CREB3L3-related_disorder": 2,
    "not_provided|Hypertriglyceridemia_2": 4,
    "Hypertriglyceridemia_2": 1,
    "Hypertriglyceridemia_2|not_provided": 2,
    "CREB3L3-related_disorder|not_provided|Hypertriglyceridemia_2": 1,
    "CREB3L3-related_disorder|not_provided": 2,
    "Hypertriglyceridemia_1|Episodic_kinesigenic_dyskinesia_1|not_provided": 1,
    "not_specified|Hypertriglyceridemia_1|not_provided|Hypertriglyceridemia_2": 1,
    "CREB3L3-related_disorder": 4,
    "Hypertriglyceridemia_2|not_provided|not_specified": 1,
    "Vacuolar_Neuromyopathy": 1,
    "Inborn_genetic_diseases|SEMA6B-related_disorder": 3,
    "SEMA6B-related_disorder": 11,
    "Epilepsy|_progressive_myoclonic|_11|Inborn_genetic_diseases": 1,
    "Epilepsy|_progressive_myoclonic|_11": 19,
    "Epilepsy|_progressive_myoclonic|_11|Intellectual_disability|not_provided": 1,
    "SEMA6B-related_disorder|Optic_atrophy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Epilepsy|_progressive_myoclonic|_11": 1,
    "Epilepsy|_progressive_myoclonic|_11|not_provided": 7,
    "not_provided|SEMA6B-related_disorder": 4,
    "Inborn_genetic_diseases|SEMA6B-related_disorder|Optic_atrophy|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|Grade_I_preterm_intraventricular_hemorrhage|Isolated_unilateral_hemispheric_cerebellar_hypoplasia": 1,
    "SEMA6B-related_disorder|not_provided": 2,
    "SEMA6B-related_disorder|Optic_atrophy|Retinal_dystrophy": 1,
    "not_provided|SEMA6B-related_disorder|Epilepsy|_progressive_myoclonic|_11": 1,
    "Hatipoglu_immunodeficiency_syndrome": 9,
    "not_specified|Hatipoglu_immunodeficiency_syndrome": 1,
    "Hatipoglu_immunodeficiency_syndrome|not_specified": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_4": 304,
    "not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_4": 21,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_4": 7,
    "TICAM1-related_disorder|Herpes_simplex_encephalitis|_susceptibility_to|_4": 4,
    "Herpes_simplex_encephalitis|_susceptibility_to|_4|not_specified": 22,
    "Herpes_simplex_encephalitis|_susceptibility_to|_4|TICAM1-related_disorder": 5,
    "Susceptibility_to_severe_COVID-19|not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_4": 1,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_4|TICAM1-related_disorder": 1,
    "not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_4|not_specified": 2,
    "not_provided|not_specified|Herpes_simplex_encephalitis|_susceptibility_to|_4": 1,
    "not_provided|TICAM1-related_disorder|Herpes_simplex_encephalitis|_susceptibility_to|_4": 1,
    "TICAM1-related_disorder": 1,
    "Herpes_simplex_encephalitis|_susceptibility_to|_4|not_provided": 6,
    "Herpes_simplex_encephalitis|_susceptibility_to|_4|not_specified|not_provided": 1,
    "TICAM1-related_disorder|not_provided|Herpes_simplex_encephalitis|_susceptibility_to|_4": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_65": 38,
    "KDM4B-related_disorder": 11,
    "not_provided|KDM4B-related_disorder": 2,
    "not_specified|Intellectual_developmental_disorder|_autosomal_dominant_65": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_65|Syndromic_global_developmental_delay": 1,
    "Neurodevelopmental_abnormality|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_65|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_65": 5,
    "Inborn_genetic_diseases|KDM4B-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|KDM4B-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_65|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_dominant_65": 1,
    "KDM4B-related_disorder|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_delay|Intellectual_developmental_disorder|_autosomal_dominant_65": 1,
    "PTPRS-related_disorder": 67,
    "not_provided|PTPRS-related_disorder": 16,
    "PTPRS-related_disorder|not_provided": 6,
    "PTPRS-related_disorder|not_specified": 1,
    "not_specified|PTPRS-related_disorder": 1,
    "Combined_oxidative_phosphorylation_deficiency_37|not_provided": 2,
    "not_provided|MICOS13-related_disorder": 1,
    "MICOS13-related_disorder": 2,
    "Combined_oxidative_phosphorylation_deficiency_37|Mitochondrial_hepato-encephalopathy": 1,
    "Combined_oxidative_phosphorylation_deficiency_37": 1,
    "CODAS_syndrome": 14,
    "CODAS_syndrome|not_provided": 7,
    "not_provided|CODAS_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|LONP1-related_disorder": 24,
    "LONP1-related_disorder|not_provided": 19,
    "Inborn_genetic_diseases|not_provided|CODAS_syndrome": 2,
    "not_provided|CODAS_syndrome": 8,
    "CODAS_syndrome|LONP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CODAS_syndrome|LONP1-related_disorder": 1,
    "LONP1-related_disorder": 8,
    "LONP1-related_disorder|Neurodevelopmental_disorder|CODAS_syndrome|not_provided": 1,
    "CODAS_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "CODAS_syndrome|not_provided|LONP1-related_disorder": 1,
    "LONP1-related_disorder|CODAS_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|CODAS_syndrome|See_cases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|CODAS_syndrome": 1,
    "LONP1-related_disorder|not_specified|not_provided|CODAS_syndrome|See_cases": 1,
    "not_specified|LONP1-related_disorder|not_provided": 1,
    "not_provided|LONP1-related_disorder|Inborn_genetic_diseases|CODAS_syndrome": 1,
    "Inborn_genetic_diseases|LONP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|CODAS_syndrome|not_specified|not_provided": 1,
    "not_provided|LONP1-related_disorder|Inborn_genetic_diseases": 1,
    "NRTN-related_disorder": 5,
    "not_specified|NRTN-related_disorder": 1,
    "not_provided|Fucosyltransferase_6_deficiency": 2,
    "FUT6-related_disorder|Fucosyltransferase_6_deficiency|not_provided": 1,
    "Fucosyltransferase_6_deficiency": 1,
    "FUT6-related_disorder": 1,
    "FUT3-related_disorder": 7,
    "not_provided|FUT3-related_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_14": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_14": 7,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_14": 1,
    "NDUFA11-related_disorder|not_provided": 3,
    "NDUFA11-related_disorder": 4,
    "not_provided|NDUFA11-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|NDUFA11-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_14|not_provided": 1,
    "CAPS-related_disorder": 4,
    "not_provided|CAPS-related_disorder": 1,
    "not_specified|Tooth_agenesis": 1,
    "RFX2-related_disorder": 1,
    "Hypertelorism|Hypotonia|Abnormal_cortical_gyration|Infantile_spasms|Cerebral_atrophy|Short_nose|Global_developmental_delay": 1,
    "Perrault_syndrome_3": 11,
    "not_provided|not_specified|Perrault_syndrome_3": 1,
    "Perrault_syndrome_3|not_provided": 3,
    "not_provided|CLPP-related_disorder": 3,
    "not_provided|Perrault_syndrome_3": 3,
    "Perrault_syndrome_3|Autosomal_recessive_hearing_impairment_with_normal_menstrual_cycles|Perrault_syndrome": 1,
    "not_provided|CLPP-related_disorder|not_specified": 1,
    "CLPP-related_disorder": 2,
    "CLPP-related_disorder|not_provided|not_specified": 1,
    "CLPP-related_disorder|not_provided": 2,
    "Perrault_syndrome_3|Perrault_syndrome": 2,
    "Inborn_genetic_diseases|CLPP-related_disorder": 1,
    "Dystonic_disorder|Hypomyelinating_leukodystrophy_6": 1,
    "Hypomyelinating_leukodystrophy_6|Torsion_dystonia_4|not_provided": 3,
    "Hypomyelinating_leukodystrophy_6|Torsion_dystonia_4": 19,
    "Torsion_dystonia_4|Hypomyelinating_leukodystrophy_6": 3,
    "not_provided|Hypomyelinating_leukodystrophy_6|Torsion_dystonia_4": 1,
    "Hypomyelinating_leukodystrophy_6|not_provided|Torsion_dystonia_4": 5,
    "Hypomyelinating_leukodystrophy_6|not_specified|Torsion_dystonia_4": 1,
    "Hypomyelinating_leukodystrophy_6": 153,
    "Hypomyelinating_leukodystrophy_6|not_provided": 18,
    "not_provided|Hypomyelinating_leukodystrophy_6": 16,
    "Torsion_dystonia_4|Hypomyelinating_leukodystrophy_6|not_provided": 5,
    "Torsion_dystonia_4": 4,
    "Hypomyelinating_leukodystrophy_6|not_specified|not_provided|Torsion_dystonia_4": 3,
    "Hypomyelinating_leukodystrophy_6|Torsion_dystonia_4|not_provided|Global_developmental_delay|Cerebral_palsy": 1,
    "TUBB4A-related_disorder|Hypomyelinating_leukodystrophy_6|not_provided": 2,
    "Abnormal_basal_ganglia_MRI_signal_intensity|Cerebral_hypomyelination|Aplasia/Hypoplasia_of_the_cerebellum|Microcephaly|Global_developmental_delay|Tetraplegia/tetraparesis|Hypomyelinating_leukodystrophy_6|not_provided": 1,
    "Hypomyelinating_leukodystrophy_6|TUBB4A-related_disorder|not_provided|Torsion_dystonia_4": 2,
    "not_provided|Hypomyelinating_leukodystrophy_6|TUBB4A-related_disorder": 2,
    "Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_6": 2,
    "not_provided|not_specified|Torsion_dystonia_4|TUBB4A-related_disorder|Hypomyelinating_leukodystrophy_6": 1,
    "not_specified|Hypomyelinating_leukodystrophy_6|not_provided|Torsion_dystonia_4": 1,
    "Hypomyelinating_leukodystrophy_6|Inborn_genetic_diseases": 1,
    "Hypomyelinating_leukodystrophy_6|Torsion_dystonia_4|TUBB4A-related_disorder|not_provided|not_specified": 1,
    "not_provided|Torsion_dystonia_4": 1,
    "Brown_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Auditory_neuropathy_spectrum_disorder|Hypomyelinating_leukodystrophy_6": 1,
    "not_provided|Hypomyelinating_leukodystrophy_6|Cerebral_palsy|Torsion_dystonia_4|Inborn_genetic_diseases|Microcephaly": 1,
    "Torsion_dystonia_4|Hypomyelinating_leukodystrophy_6|not_provided|Abnormality_of_the_nervous_system": 1,
    "Leukodystrophy|Hypomyelinating_leukodystrophy_6|not_provided": 1,
    "TUBB4A-related_disorder": 3,
    "Hypomyelinating_leukodystrophy_6|not_provided|TUBB4A-related_disorder": 1,
    "not_specified|Hypomyelinating_leukodystrophy_6": 2,
    "Torsion_dystonia_4|not_provided": 1,
    "TUBB4A-related_disorder|Inborn_genetic_diseases|Hypomyelinating_leukodystrophy_6": 1,
    "Hypomyelinating_leukodystrophy_6|TUBB4A-related_disorder": 1,
    "TUBB4A-related_disorder|Hypomyelinating_leukodystrophy_6|Inborn_genetic_diseases": 1,
    "Hypomyelinating_leukodystrophy_6|not_specified": 1,
    "TUBB4A-related_disorder|Hypomyelinating_leukodystrophy_6|Torsion_dystonia_4": 1,
    "TUBB4A-related_hypomyelinating_leukodystrophy_and/or_torsion_dystonia": 1,
    "CD70-related_disorder": 4,
    "Severe_combined_immunodeficiency_due_to_CD70_deficiency": 3,
    "not_provided|CD70-related_disorder": 1,
    "not_specified|CD70-related_disorder|not_provided": 1,
    "not_provided|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9": 12,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Age_related_macular_degeneration_9|not_provided": 5,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 108,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided": 9,
    "not_specified|Complement_component_3_deficiency|not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis": 1,
    "not_provided|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 15,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Kidney_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3-related_disorder|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided|Age_related_macular_degeneration_9": 1,
    "C3-related_disorder|not_specified|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_provided": 9,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "C3-related_disorder|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "Age_related_macular_degeneration_9|not_provided|C3-related_disorder|not_specified|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis": 63,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_specified|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided|C3-related_disorder": 1,
    "not_specified|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "not_specified|C3-related_disorder|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided": 10,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 18,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "Complement_component_3_deficiency|C3_DEFICIENCY": 2,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 18,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 2,
    "Inborn_genetic_diseases|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Complement_component_3_deficiency": 24,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided": 6,
    "Complement_component_3_deficiency|C3_glomerulonephritis|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "C3_glomerulonephritis|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided": 1,
    "Complement_component_3_deficiency|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 4,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|not_provided": 2,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Complement_component_3_deficiency|not_provided": 6,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|C3_glomerulonephritis|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "Complement_component_3_deficiency|not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 6,
    "not_provided|C3-related_disorder|not_specified": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis": 2,
    "not_provided|C3-related_disorder": 3,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 3,
    "not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "C3-related_disorder": 5,
    "not_provided|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 8,
    "Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome": 2,
    "Atypical_hemolytic-uremic_syndrome|Macular_degeneration|C3_DEFICIENCY": 2,
    "not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_specified": 1,
    "C3_glomerulonephritis|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_specified|not_provided": 1,
    "C3_DEFICIENCY|not_provided": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9": 1,
    "Atypical_hemolytic-uremic_syndrome|not_provided|not_specified": 1,
    "C3-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency": 2,
    "C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "not_provided|not_specified|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Complement_component_3_deficiency|not_provided": 1,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided": 2,
    "not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 9,
    "not_provided|not_specified|C3-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_provided|C3_glomerulonephritis|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 1,
    "C3-related_disorder|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "C3-related_disorder|not_specified|Complement_component_3_deficiency|not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis": 1,
    "C3-related_disorder|not_provided|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 4,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 3,
    "not_provided|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Atypical_hemolytic-uremic_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Atypical_hemolytic-uremic_syndrome": 2,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "not_provided|Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Complement_component_3_deficiency": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 1,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|Inborn_genetic_diseases": 1,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|not_provided|Factor_I_deficiency": 1,
    "not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 3,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3-related_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|C3-related_disorder|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided": 1,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified": 1,
    "Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "C3-related_disorder|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "not_provided|C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|not_provided": 1,
    "Age_related_macular_degeneration_9|not_provided|not_specified|Complement_component_3_deficiency": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Age_related_macular_degeneration_9|not_provided|C3-related_disorder|Atypical_hemolytic-uremic_syndrome": 1,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9": 4,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "Age_related_macular_degeneration_9|not_provided|Complement_component_3_deficiency": 6,
    "C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|not_provided|not_specified|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "C3-related_disorder|not_provided": 2,
    "C3-related_disorder|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 1,
    "not_provided|C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 4,
    "Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 3,
    "Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency": 1,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|C3-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_glomerulonephritis": 1,
    "Retinal_dystrophy|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided|not_specified": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 4,
    "not_specified|Complement_component_3_deficiency|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|not_specified|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "C3_DEFICIENCY|Macular_degeneration|Atypical_hemolytic-uremic_syndrome": 1,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Complement_component_3_deficiency|not_provided|Age_related_macular_degeneration_9": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|C3_glomerulonephritis": 1,
    "not_provided|Inborn_genetic_diseases|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_provided|not_specified|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|Age_related_macular_degeneration_9": 4,
    "Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|not_specified": 2,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Complement_component_3_deficiency": 1,
    "Atypical_hemolytic-uremic_syndrome|Macular_degeneration|not_provided|C3_DEFICIENCY": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_specified|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "not_provided|Familial_hemolytic_anemia": 1,
    "Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided|C3-related_disorder": 1,
    "not_specified|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_provided": 2,
    "Complement_component_3_deficiency|C3_glomerulonephritis|Kidney_disorder|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Premature_ovarian_failure|not_provided": 1,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|C3_glomerulonephritis": 1,
    "C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Familial_Atypical_Hemolytic-Uremic_Syndrome|C3-related_disorder|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_provided": 1,
    "not_provided|Familial_Atypical_Hemolytic-Uremic_Syndrome|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "C3_DEFICIENCY|Macular_degeneration|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|C3-related_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Inborn_genetic_diseases|Complement_component_3_deficiency": 1,
    "C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|not_provided": 2,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 1,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|C3-related_disorder": 1,
    "Complement_component_3_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|C3_glomerulonephritis|not_provided": 1,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Kidney_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|C3-related_disorder|not_provided": 1,
    "Age_related_macular_degeneration_9|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 2,
    "not_specified|not_provided|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9": 1,
    "C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|C3-related_disorder|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 1,
    "not_specified|C3-related_disorder|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 2,
    "Inborn_genetic_diseases|not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 1,
    "Age_related_macular_degeneration_9|not_provided|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "Inborn_genetic_diseases|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "Inborn_genetic_diseases|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|not_provided|C3-related_disorder": 1,
    "Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3-related_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency|not_provided|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|Inborn_genetic_diseases|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_POLYMORPHISM|_HAV_4-1_PLUS/MINUS_TYPE|Focal_segmental_glomerulosclerosis": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Age_related_macular_degeneration_9|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 2,
    "Atypical_hemolytic-uremic_syndrome|not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|Complement_component_3_deficiency|Age_related_macular_degeneration_9": 1,
    "C3_glomerulonephritis|not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|Complement_component_3_deficiency": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3-related_disorder|not_provided|Age_related_macular_degeneration_9": 1,
    "Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_glomerulonephritis": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 1,
    "C3_glomerulonephritis|Complement_component_3_deficiency|not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly": 2,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|not_specified|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_provided|Age_related_macular_degeneration_9": 1,
    "C3-related_disorder|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Age_related_macular_degeneration_9|not_provided": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "C3-related_disorder|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome|Complement_component_3_deficiency|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|Retinal_dystrophy|not_provided|MACULAR_DEGENERATION|_AGE-RELATED|_9|_SUSCEPTIBILITY_TO": 1,
    "C3_glomerulonephritis|Complement_component_3_deficiency|Atypical_hemolytic-uremic_syndrome|Inborn_genetic_diseases|not_provided|Age_related_macular_degeneration_9|MACULAR_DEGENERATION|_AGE-RELATED|_9|_SUSCEPTIBILITY_TO|C3S/C3F_POLYMORPHISM|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|not_specified|Complement_component_3_deficiency|Age_related_macular_degeneration_9|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome": 1,
    "not_provided|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome|C3_glomerulonephritis|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 1,
    "not_specified|Atypical_hemolytic-uremic_syndrome|Macular_degeneration|not_provided|C3_glomerulonephritis|Complement_component_3_deficiency|C3_DEFICIENCY": 1,
    "Atypical_hemolytic-uremic_syndrome|Age_related_macular_degeneration_9|Atypical_hemolytic-uremic_syndrome_with_C3_anomaly|Complement_component_3_deficiency": 1,
    "not_provided|VAV1-related_disorder": 7,
    "not_provided|not_specified|VAV1-related_disorder": 1,
    "VAV1-related_disorder|not_specified|not_provided": 1,
    "VAV1-related_disorder|not_provided": 4,
    "Attention_deficit_hyperactivity_disorder|Precocious_puberty|Autism|Anxiety|Tremor|Hearing_impairment|Autistic_behavior|Expressive_language_delay|Hyperactivity|Pes_planus|Macrocephaly": 1,
    "not_provided|VAV1-related_disorder|not_specified": 1,
    "ADGRE1-related_disorder|not_provided": 1,
    "ADGRE1-related_disorder": 2,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 18,
    "not_provided|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 2,
    "Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 42,
    "Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Rabson-Mendenhall_syndrome": 16,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome": 30,
    "not_provided|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 17,
    "Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome": 32,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 11,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|not_provided|Rabson-Mendenhall_syndrome": 2,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 2,
    "Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|not_provided": 2,
    "not_provided|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome": 4,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome": 1,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|not_provided|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 4,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 12,
    "INSR-related_disorder|not_provided": 7,
    "Rabson-Mendenhall_syndrome": 12,
    "INSR-related_disorder": 17,
    "not_specified|not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "Hyperinsulinism_due_to_INSR_deficiency": 6,
    "Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "not_provided|Insulin_resistance": 1,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "Insulin_resistance|not_provided": 1,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 3,
    "Leprechaunism_syndrome": 19,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Insulin_resistance": 1,
    "not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|not_provided": 1,
    "Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_provided|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 2,
    "Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|not_specified|not_provided": 1,
    "Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "not_provided|INSR-related_disorder": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_specified|not_provided|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|not_provided": 1,
    "Monogenic_diabetes|Bailey-Bloch_congenital_myopathy|not_provided|not_specified|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Type_2_diabetes_mellitus": 1,
    "not_provided|not_specified|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "not_specified|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Monogenic_diabetes|INSR-related_disorder|not_provided": 1,
    "not_provided|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 2,
    "not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "INSR-related_disorder|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Monogenic_diabetes|not_provided|not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "not_specified|not_provided|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency": 3,
    "INSR-related_disorder|not_specified|not_provided|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 1,
    "not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Leprechaunism_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_provided|INSR-related_disorder": 1,
    "INSR-related_disorder|Monogenic_diabetes|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|not_provided": 1,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|not_provided": 1,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 3,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Monogenic_diabetes|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Inborn_genetic_diseases|not_provided|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "not_specified|INSR-related_disorder|not_provided|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "INSR-related_disorder|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|not_specified|INSR-related_disorder|not_provided": 1,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|See_cases": 1,
    "not_specified|INSR-related_disorder|Inborn_genetic_diseases|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_provided|Monogenic_diabetes": 1,
    "not_specified|not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|not_provided|Rabson-Mendenhall_syndrome|not_specified": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Inborn_genetic_diseases": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|not_provided": 1,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|not_provided": 1,
    "Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_provided": 2,
    "not_provided|Leprechaunism_syndrome": 2,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|not_provided|not_specified": 1,
    "not_specified|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided|Leprechaunism_syndrome": 1,
    "Inborn_genetic_diseases|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 1,
    "not_specified|INSR-related_disorder|not_provided": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|not_provided": 1,
    "not_provided|not_specified|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|INSR-related_disorder": 1,
    "Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "Leprechaunism_syndrome|INSR-related_disorder": 1,
    "Insulin-resistant_diabetes_mellitus": 1,
    "not_provided|INSR-related_disorder|not_specified": 1,
    "INSR-related_disorder|not_provided|not_specified": 2,
    "not_provided|Rabson-Mendenhall_syndrome": 1,
    "Leprechaunism_syndrome|not_specified|not_provided|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "not_provided|not_specified|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|not_specified|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided|INSR-related_disorder": 1,
    "INSR-related_disorder|not_specified|not_provided": 2,
    "not_provided|INSR-related_disorder|not_specified|Leprechaunism_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "not_provided|not_specified|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "not_provided|not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome": 1,
    "Inborn_genetic_diseases|Hyperinsulinism_due_to_INSR_deficiency": 1,
    "Rabson-Mendenhall_syndrome|not_specified|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome": 1,
    "Rabson-Mendenhall_syndrome|not_specified": 1,
    "not_specified|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|not_provided": 1,
    "Leprechaunism_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|not_specified": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Leprechaunism_syndrome|not_specified|Hyperinsulinism_due_to_INSR_deficiency|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 2,
    "INSR-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Type_2_diabetes_mellitus|not_provided": 1,
    "not_provided|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome": 1,
    "Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Rabson-Mendenhall_syndrome|Leprechaunism_syndrome|not_provided": 1,
    "not_specified|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "not_specified|INSR-related_disorder|Monogenic_diabetes": 1,
    "Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|INSR-related_disorder|not_provided|not_specified": 1,
    "not_specified|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|not_provided": 1,
    "not_specified|INSR-related_disorder": 1,
    "not_provided|Monogenic_diabetes|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Hyperinsulinism_due_to_INSR_deficiency|Inborn_genetic_diseases": 1,
    "INSR-related_disorder|Hyperinsulinism_due_to_INSR_deficiency|not_provided|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "Inborn_genetic_diseases|not_specified|Hyperinsulinism_due_to_INSR_deficiency|Leprechaunism_syndrome|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans": 1,
    "not_provided|Rabson-Mendenhall_syndrome|Insulin-resistant_diabetes_mellitus_AND_acanthosis_nigricans|Leprechaunism_syndrome|not_specified": 1,
    "Retinitis_pigmentosa_78": 7,
    "Inborn_genetic_diseases|not_provided|ARHGEF18-related_disorder": 1,
    "Retinitis_pigmentosa_78|not_provided": 7,
    "not_provided|ARHGEF18-related_disorder": 15,
    "not_provided|Retinitis_pigmentosa_78|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|ARHGEF18-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|ARHGEF18-related_disorder": 2,
    "ARHGEF18-related_disorder|not_provided": 8,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_78": 1,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_78|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_78": 2,
    "Retinal_dystrophy|Retinitis_pigmentosa_78|not_provided": 1,
    "ARHGEF18-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|ARHGEF18-related_disorder|not_provided": 1,
    "Mucolipidosis_type_IV": 719,
    "Inborn_genetic_diseases|Mucolipidosis_type_IV": 28,
    "Lisch_epithelial_corneal_dystrophy|Mucolipidosis_type_IV": 13,
    "not_provided|Mucolipidosis_type_IV": 21,
    "Mucolipidosis_type_IV|Inborn_genetic_diseases": 14,
    "Mucolipidosis_type_IV|not_provided": 15,
    "Inborn_genetic_diseases|not_provided|Mucolipidosis_type_IV": 3,
    "MCOLN1-related_disorder|Mucolipidosis_type_IV": 3,
    "not_provided|Inborn_genetic_diseases|Mucolipidosis_type_IV": 4,
    "Mucolipidosis_type_IV|Lisch_epithelial_corneal_dystrophy": 6,
    "Inborn_genetic_diseases|Mucolipidosis_type_IV|MCOLN1-related_disorder": 1,
    "Mucolipidosis_type_IV|MCOLN1-related_disorder": 3,
    "not_provided|Mucolipidosis_type_IV|Lisch_epithelial_corneal_dystrophy|MCOLN1-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Mucolipidosis_type_IV": 1,
    "Growth_delay|Intellectual_disability|Delayed_myelination|Periventricular_leukomalacia|Atrophy/Degeneration_affecting_the_brainstem|Corneal_opacity|Delayed_speech_and_language_development": 1,
    "Mucolipidosis_type_IV|MCOLN1-related_disorder|not_provided": 1,
    "Mucolipidosis_type_IV|Lisch_epithelial_corneal_dystrophy|Mucolipidosis|not_provided": 1,
    "Inborn_genetic_diseases|Mucolipidosis_type_IV|not_provided": 2,
    "not_specified|Mucolipidosis_type_IV": 4,
    "Inborn_genetic_diseases|Mucolipidosis_type_IV|See_cases": 1,
    "not_provided|Mucolipidosis_type_IV|Lisch_epithelial_corneal_dystrophy": 1,
    "MCOLN1-related_disorder": 1,
    "Mucolipidosis_type_IV|Delayed_myelination|Atrophy/Degeneration_affecting_the_brainstem|Corneal_opacity|Periventricular_leukomalacia|Delayed_speech_and_language_development|Growth_delay|Intellectual_disability": 1,
    "Lisch_epithelial_corneal_dystrophy|Mucolipidosis_type_IV|not_specified|not_provided": 1,
    "not_provided|Mucolipidosis_type_IV|Inborn_genetic_diseases": 2,
    "Mucolipidosis_type_IV|not_provided|Inborn_genetic_diseases": 1,
    "Mucolipidosis_type_IV|Lisch_epithelial_corneal_dystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Mucolipidosis_type_IV|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Mucolipidosis_type_IV": 1,
    "not_specified|not_provided|Mucolipidosis_type_IV": 1,
    "Lisch_epithelial_corneal_dystrophy|Mucolipidosis_type_IV|MCOLN1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Lisch_epithelial_corneal_dystrophy|Mucolipidosis_type_IV": 1,
    "Mucolipidosis_type_IV|not_specified": 1,
    "not_provided|Spastic_Paraplegia|_Recessive|Mucolipidosis_type_IV": 1,
    "Mucolipidosis_type_IV|Hereditary_spastic_paraplegia_39": 1,
    "Mucolipidosis_type_IV|Inborn_genetic_diseases|MCOLN1-related_disorder": 1,
    "Hereditary_spastic_paraplegia_39": 946,
    "not_provided|Hereditary_spastic_paraplegia_39|Mucolipidosis_type_IV": 2,
    "Mucolipidosis_type_IV|not_provided|Hereditary_spastic_paraplegia_39|Spastic_Paraplegia|_Recessive": 1,
    "PNPLA6-related_spastic_paraplegia_with_or_without_ataxia": 1,
    "not_specified|Hereditary_spastic_paraplegia_39": 8,
    "not_provided|Hereditary_spastic_paraplegia_39": 39,
    "Retinal_dystrophy|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_39|not_provided": 27,
    "Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39": 20,
    "PNPLA6-related_disorder|not_provided|not_specified|Hereditary_spastic_paraplegia_39": 1,
    "not_specified|Hereditary_spastic_paraplegia|Spastic_Paraplegia|_Recessive|Hereditary_spastic_paraplegia_39|Mucolipidosis_type_IV": 1,
    "Mucolipidosis_type_IV|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39|Spastic_Paraplegia|_Recessive|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia|Spastic_Paraplegia|_Recessive|Mucolipidosis_type_IV|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_39|Inborn_genetic_diseases": 22,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|not_specified": 1,
    "Hereditary_spastic_paraplegia_39|not_specified": 13,
    "PNPLA6-related_disorder|Hereditary_spastic_paraplegia_39": 3,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39|not_provided|Retinal_dystrophy": 1,
    "PNPLA6-related_disorder": 4,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_39": 1,
    "Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 4,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|not_provided": 2,
    "Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Hereditary_spastic_paraplegia_39": 1,
    "Hereditary_spastic_paraplegia_39|Marfanoid_habitus_and_intellectual_disability|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39|not_provided": 3,
    "not_provided|Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia|not_specified": 1,
    "HP:0000365": 1,
    "Hereditary_spastic_paraplegia_39|Inborn_genetic_diseases|not_provided": 4,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39": 3,
    "Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Cerebellar_ataxia|Dysarthria": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|PNPLA6-related_disorder": 1,
    "Hereditary_spastic_paraplegia_39|PNPLA6-related_disorder": 9,
    "not_provided|Hereditary_spastic_paraplegia_39|not_specified": 2,
    "not_provided|Hereditary_spastic_paraplegia_39|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39": 3,
    "Hereditary_spastic_paraplegia_39|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Peripheral_neuropathy|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia_39|not_provided": 2,
    "not_provided|Hereditary_spastic_paraplegia_39|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|Inborn_genetic_diseases": 1,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 8,
    "Hereditary_spastic_paraplegia_39|not_specified|not_provided": 1,
    "Laurence-Moon_syndrome|Hereditary_spastic_paraplegia_39|not_specified|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39": 2,
    "Hereditary_spastic_paraplegia_39|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39": 1,
    "not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|not_provided": 1,
    "Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome": 1,
    "Retinal_dystrophy|Hereditary_spastic_paraplegia_39": 1,
    "Laurence-Moon_syndrome": 3,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39": 5,
    "not_provided|not_specified|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39": 3,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Cerebellar_ataxia-hypogonadism_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome": 1,
    "not_provided|not_specified|Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_39|not_provided|not_specified": 2,
    "Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "Hereditary_spastic_paraplegia_39|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_provided": 2,
    "PNPLA6-related_disorder|not_specified|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_39": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_39": 2,
    "Hereditary_spastic_paraplegia_39|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|not_provided|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 1,
    "Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|not_provided|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 1,
    "not_provided|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_specified": 1,
    "Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia|not_provided|not_specified": 1,
    "Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_specified|not_provided": 1,
    "Amyotrophic_lateral_sclerosis|Hereditary_spastic_paraplegia_39": 1,
    "Hereditary_spastic_paraplegia_39|Spastic_ataxia": 1,
    "PNPLA6-related_disorder|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Retinal_dystrophy|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_39|not_provided|Hereditary_spastic_paraplegia": 1,
    "Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39|not_provided|Inborn_genetic_diseases": 1,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_provided|Hereditary_spastic_paraplegia_39": 1,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39": 3,
    "PNPLA6-related_disorder|Hereditary_spastic_paraplegia_39|not_specified|not_provided": 1,
    "PNPLA6-related_disorder|Hereditary_spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_39": 1,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_provided|Hereditary_spastic_paraplegia_39|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome": 1,
    "not_provided|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39": 1,
    "Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 1,
    "Cerebellar_atrophy|Dysarthria|Gait_ataxia|Hereditary_spastic_paraplegia_39": 1,
    "Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|not_provided|Laurence-Moon_syndrome": 1,
    "Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|PNPLA6-related_disorder|not_specified": 1,
    "Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|not_provided|Hereditary_spastic_paraplegia_39|Retinal_dystrophy": 1,
    "not_provided|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Cerebellar_ataxia-hypogonadism_syndrome|Rod-cone_dystrophy|Hereditary_spastic_paraplegia_39": 1,
    "Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_39|Laurence-Moon_syndrome|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome": 1,
    "Hereditary_spastic_paraplegia_39|not_provided|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 1,
    "Hereditary_spastic_paraplegia_39|Laurence-Moon_syndrome|not_provided|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome": 1,
    "Hereditary_spastic_paraplegia_39|PNPLA6-related_disorder|Hereditary_spastic_paraplegia": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_39": 1,
    "Laurence-Moon_syndrome|Hereditary_spastic_paraplegia_39": 1,
    "Hereditary_spastic_paraplegia_39|not_specified|PNPLA6-related_disorder": 1,
    "not_provided|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|Laurence-Moon_syndrome": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_39|not_specified|PNPLA6-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_39|Amenorrhea": 1,
    "Hereditary_spastic_paraplegia_39|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_39|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Laurence-Moon_syndrome": 1,
    "Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia": 1,
    "Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Dysarthria|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Cerebellar_ataxia|not_provided|Gait_ataxia|Cerebellar_atrophy|Hereditary_spastic_paraplegia_39|PNPLA6-related_disorder": 1,
    "Laurence-Moon_syndrome|Ataxia-hypogonadism-choroidal_dystrophy_syndrome|Hereditary_spastic_paraplegia_39|Trichomegaly-retina_pigmentary_degeneration-dwarfism_syndrome|not_provided|Hereditary_spastic_paraplegia": 1,
    "PNPLA6-related_disorder|Hereditary_spastic_paraplegia_39|not_provided": 1,
    "not_specified|Hereditary_spastic_paraplegia_39|PNPLA6-related_disorder": 1,
    "PNPLA6-related_disorder|Hereditary_spastic_paraplegia_39|Hereditary_spastic_paraplegia": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 8,
    "PET100-related_disorder|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_12|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 5,
    "PET100-related_disorder|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 1,
    "PET100-related_disorder|not_provided": 1,
    "not_provided|PET100-related_disorder": 2,
    "Abnormality_of_the_mitochondrion|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 1,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_12|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Congenital_lactic_acidosis|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_12": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5": 908,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 14,
    "Familial_hemophagocytic_lymphohistiocytosis_5|STXBP2-related_disorder": 12,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis|not_specified|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Inborn_genetic_diseases": 12,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_specified": 6,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|not_provided": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_5|not_provided": 4,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 6,
    "Familial_hemophagocytic_lymphohistiocytosis_5|STXBP2-related_disorder|not_provided": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_5": 20,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "HEMOPHAGOCYTIC_LYMPHOHISTIOCYTOSIS|_FAMILIAL|_5|_WITHOUT_MICROVILLUS_INCLUSION_DISEASE": 2,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_5": 3,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_provided": 9,
    "STXBP2-related_disorder|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome": 5,
    "STXBP2-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_5": 6,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|Inborn_genetic_diseases": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_5|not_specified|Autoinflammatory_syndrome": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_5": 14,
    "Inborn_genetic_diseases|not_specified|Thrombocytopenia|Abnormal_bleeding|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_specified|not_provided": 2,
    "STXBP2-related_disorder": 7,
    "not_specified|Autoinflammatory_syndrome|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_5|not_provided": 1,
    "HEMOPHAGOCYTIC_LYMPHOHISTIOCYTOSIS|_FAMILIAL|_5|_WITHOUT_MICROVILLUS_INCLUSION_DISEASE|not_specified": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Inborn_genetic_diseases|not_provided": 2,
    "Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_5": 3,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_provided|STXBP2-related_disorder": 1,
    "STXBP2-related_disorder|Autoinflammatory_syndrome|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|STXBP2-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "STXBP2-related_disorder|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|not_specified": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_5|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis|STXBP2-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_provided|Autoinflammatory_syndrome": 1,
    "not_specified|STXBP2-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 2,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|STXBP2-related_disorder|Autoinflammatory_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_provided|Autoinflammatory_syndrome|not_specified": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|not_specified": 3,
    "HEMOPHAGOCYTIC_LYMPHOHISTIOCYTOSIS|_FAMILIAL|_5|_WITHOUT_MICROVILLUS_INCLUSION_DISEASE|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|STXBP2-related_disorder": 1,
    "STXBP2-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_5|Familial_hemophagocytic_lymphohistiocytosis": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis|Familial_hemophagocytic_lymphohistiocytosis_5|not_specified": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|STXBP2-related_disorder": 2,
    "Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_5|not_provided": 1,
    "not_specified|Familial_hemophagocytic_lymphohistiocytosis_5|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_5|STXBP2-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "not_provided|Inborn_genetic_diseases|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "not_specified|not_provided|Familial_hemophagocytic_lymphohistiocytosis|STXBP2-related_disorder|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_5|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_provided|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome|not_specified": 2,
    "STXBP2-related_disorder|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Familial_hemophagocytic_lymphohistiocytosis|not_provided|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "not_provided|STXBP2-related_disorder|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_5": 1,
    "not_provided|not_specified|Familial_hemophagocytic_lymphohistiocytosis_5|Autoinflammatory_syndrome": 1,
    "RETN-related_disorder": 1,
    "Diabetes_mellitus_type_2|_susceptibility_to|HYPERTENSION|_INSULIN_RESISTANCE-RELATED|_SUSCEPTIBILITY_TO": 1,
    "CD209-related_disorder": 2,
    "not_provided|Mycobacterium_tuberculosis|_susceptibility_to|Dengue_virus|_susceptibility_to|Susceptibility_to_HIV_infection|CD209-related_disorder": 1,
    "not_provided|Dengue_virus|_susceptibility_to|Susceptibility_to_HIV_infection|Mycobacterium_tuberculosis|_susceptibility_to": 1,
    "Mycobacterium_tuberculosis|_susceptibility_to|Susceptibility_to_HIV_infection|Dengue_fever|_protection_against": 1,
    "not_provided|FBN3-related_disorder": 85,
    "not_specified|FBN3-related_disorder|not_provided": 5,
    "not_specified|not_provided|FBN3-related_disorder": 5,
    "FBN3-related_disorder": 6,
    "FBN3-related_disorder|not_provided": 53,
    "FBN3-related_disorder|not_specified|not_provided": 5,
    "not_provided|FBN3-related_disorder|not_specified": 3,
    "FBN3-related_disorder|not_provided|not_specified": 2,
    "not_provided|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect": 4,
    "Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect": 109,
    "Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect|not_provided|not_specified": 6,
    "CD320-related_disorder": 2,
    "not_specified|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect": 11,
    "not_specified|not_provided|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect": 1,
    "Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect|not_specified|not_provided": 3,
    "Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect|not_specified": 5,
    "CD320-related_disorder|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect": 2,
    "not_specified|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect|not_provided": 2,
    "Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect|not_provided": 1,
    "CD320-related_disorder|not_provided|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect": 1,
    "not_provided|Methylmalonic_acidemia_due_to_transcobalamin_receptor_defect|not_specified": 1,
    "Diamond-Blackfan_anemia_15_with_mandibulofacial_dysostosis": 1,
    "RPS28-related_disorder|not_provided": 1,
    "Diamond-Blackfan_anemia_15_with_mandibulofacial_dysostosis|not_provided": 1,
    "Plasma_triglyceride_level_quantitative_trait_locus": 3,
    "ANGPTL4-related_disorder": 7,
    "ANGPTL4-related_disorder|not_provided": 1,
    "not_provided|RAB11B-related_disorder": 5,
    "RAB11B-related_disorder|not_provided": 4,
    "Neurodevelopmental_disorder_with_ataxic_gait|_absent_speech|_and_decreased_cortical_white_matter": 6,
    "Neurodevelopmental_disorder_with_ataxic_gait|_absent_speech|_and_decreased_cortical_white_matter|not_provided": 4,
    "not_provided|RAB11B-related_disorder|Neurodevelopmental_disorder_with_ataxic_gait|_absent_speech|_and_decreased_cortical_white_matter": 1,
    "RAB11B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Neurodevelopmental_disorder_with_ataxic_gait|_absent_speech|_and_decreased_cortical_white_matter|Inborn_genetic_diseases": 1,
    "RAB11B-related_disorder": 2,
    "not_provided|Neurodevelopmental_disorder_with_ataxic_gait|_absent_speech|_and_decreased_cortical_white_matter": 1,
    "MYO1F-related_disorder": 14,
    "MYO1F-related_disorder|not_provided": 4,
    "not_specified|not_provided|MYO1F-related_disorder": 1,
    "not_specified|MYO1F-related_disorder|not_provided": 1,
    "MYO1F-related_disorder|not_specified": 2,
    "not_provided|MYO1F-related_disorder": 3,
    "not_specified|MYO1F-related_disorder": 1,
    "not_provided|not_specified|MYO1F-related_disorder": 1,
    "not_provided|Weill-Marchesani_syndrome": 39,
    "Weill-Marchesani_syndrome|not_provided": 22,
    "not_provided|Weill-Marchesani_syndrome_1": 6,
    "not_provided|Weill-Marchesani_syndrome_1|Inborn_genetic_diseases": 1,
    "Weill-Marchesani_syndrome_1": 31,
    "not_provided|Weill-Marchesani_syndrome|not_specified": 1,
    "not_specified|Weill-Marchesani_syndrome|not_provided": 1,
    "not_provided|ADAMTS10-related_disorder": 8,
    "Weill-Marchesani_syndrome|ADAMTS10-related_disorder|not_provided": 1,
    "Weill-Marchesani_syndrome|ADAMTS10-related_disorder|not_provided|Weill-Marchesani_syndrome_1": 1,
    "Weill-Marchesani_syndrome|not_provided|not_specified": 1,
    "ADAMTS10-related_disorder|not_provided": 4,
    "not_provided|ADAMTS10-related_disorder|Weill-Marchesani_syndrome": 1,
    "Weill-Marchesani_syndrome_1|Weill-Marchesani_syndrome|not_provided": 1,
    "Weill-Marchesani_syndrome_1|not_provided": 6,
    "ADAMTS10-related_disorder|not_provided|Weill-Marchesani_syndrome": 1,
    "Weill-Marchesani_syndrome|not_provided|not_specified|Weill-Marchesani_syndrome_1": 1,
    "not_provided|Weill-Marchesani_syndrome|ADAMTS10-related_disorder": 2,
    "ADAMTS10-related_disorder|Weill-Marchesani_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Weill-Marchesani_syndrome": 2,
    "ADAMTS10-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Weill-Marchesani_syndrome": 1,
    "Weill-Marchesani_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Weill-Marchesani_syndrome|not_provided": 2,
    "not_specified|Weill-Marchesani_syndrome|Weill-Marchesani_syndrome_1|not_provided": 1,
    "Weill-Marchesani_syndrome_1|not_provided|ADAMTS10-related_disorder": 1,
    "ADAMTS10-related_disorder|Weill-Marchesani_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|Weill-Marchesani_syndrome": 1,
    "Inborn_genetic_diseases|Weill-Marchesani_syndrome_1|not_provided": 1,
    "Spermatogenic_failure_53": 4,
    "ACTL9-related_disorder": 1,
    "MUC16-related_disorder": 406,
    "not_provided|MUC16-related_disorder": 45,
    "MUC16-related_disorder|not_provided": 10,
    "Ovarian_cancer|MUC16-related_disorder": 1,
    "MUC16-related_disorder|Abnormality_of_neuronal_migration": 2,
    "DEGCAGS_syndrome": 23,
    "ZNF699-related_disorder": 1,
    "DEGCAGS_syndrome|Diamond-Blackfan_anemia": 1,
    "STARGARDT_DISEASE_5": 1,
    "not_specified|ANGPTL6-related_disorder": 1,
    "ANGPTL6-related_disorder": 1,
    "Cataplexy_and_narcolepsy": 4,
    "PPAN-P2RY11-related_disorder|not_provided": 1,
    "PPAN-P2RY11-related_disorder": 6,
    "P2RY11-related_disorder": 5,
    "not_provided|PPAN-P2RY11-related_disorder": 1,
    "P2RY11-related_disorder|not_provided": 1,
    "EIF3G-related_autism_spectrum_disorder": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 989,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 68,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 6,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided": 55,
    "Dementia|_Deafness|_and_Sensory_Neuropathy": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 8,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified|not_provided": 3,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 6,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 15,
    "not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided": 8,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases": 23,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 9,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 6,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "DNMT1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|not_specified": 4,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified": 11,
    "DNMT1-related_disorder|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 5,
    "DNMT1-related_disorder|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 2,
    "Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 15,
    "Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 2,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases": 7,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified": 8,
    "Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified": 1,
    "DNMT1-related_disorder": 4,
    "not_specified|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 7,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|DNMT1-related_disorder|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_provided": 1,
    "Inborn_genetic_diseases|Beckwith-Wiedemann_syndrome|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "not_specified|DNMT1-related_disorder|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|DNMT1-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Limb-girdle_muscular_dystrophy": 1,
    "DNMT1-related_disorder|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided": 5,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|DNMT1-related_disorder": 2,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Beckwith-Wiedemann_syndrome": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|DNMT1-related_disorder|not_provided": 2,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Spastic_ataxia": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided": 3,
    "not_provided|DNMT1-related_disorder": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified|not_provided|DNMT1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 3,
    "Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Dementia|_Deafness|_and_Sensory_Neuropathy|not_specified": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|DNMT1-related_disorder": 3,
    "Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided": 3,
    "Cerebellar_ataxia|Cerebellar_atrophy|Acanthocytosis|Chorea|Dysarthria|Dysphagia|Cerebral_atrophy": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases|not_specified": 2,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|DNMT1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_specified|not_provided": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_provided": 4,
    "not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_provided": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 2,
    "Charcot-Marie-Tooth_disease|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_specified": 1,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|not_specified": 1,
    "not_provided|DNMT1-related_disorder|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Dementia|_Deafness|_and_Sensory_Neuropathy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 2,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|not_specified|Dementia|_Deafness|_and_Sensory_Neuropathy": 1,
    "not_specified|Dementia|_Deafness|_and_Sensory_Neuropathy|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "not_provided|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided": 1,
    "DNMT1-related_disorder|not_provided|not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy|not_provided": 1,
    "not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Beckwith-Wiedemann_syndrome": 1,
    "DNMT1-related_disorder|not_specified|not_provided|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Ataxia|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "Hereditary_sensory_neuropathy-deafness-dementia_syndrome|Inborn_genetic_diseases|Autosomal_dominant_cerebellar_ataxia|_deafness_and_narcolepsy": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome": 1,
    "DNMT1-related_disorder|not_specified|Hereditary_sensory_neuropathy-deafness-dementia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|S1PR2-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_68|not_provided": 1,
    "S1PR2-related_disorder|not_provided": 4,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_68|not_specified": 1,
    "not_provided|S1PR2-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_68": 2,
    "not_provided|S1PR2-related_disorder|not_specified": 1,
    "ICAM1-related_disorder": 6,
    "Malaria|_cerebral|_susceptibility_to|ICAM1-related_disorder": 1,
    "ICAM1-related_disorder|not_provided": 3,
    "not_provided|ICAM1-related_disorder": 1,
    "Landsteiner-Wiener_phenotype": 3,
    "ICAM4-related_disorder": 1,
    "not_provided|FDX2-related_disorder": 2,
    "Mitochondrial_myopathy|_episodic|_with_optic_atrophy_and_reversible_leukoencephalopathy": 1,
    "not_provided|not_specified|Mitochondrial_myopathy|_episodic|_with_optic_atrophy_and_reversible_leukoencephalopathy": 1,
    "FDX2-related_disorder|not_provided": 2,
    "not_specified|Mitochondrial_myopathy|_episodic|_with_optic_atrophy_and_reversible_leukoencephalopathy|not_provided": 1,
    "FDX2-related_disorder": 1,
    "Mitochondrial_myopathy|_episodic|_without_optic_atrophy_and_reversible_leukoencephalopathy|Inborn_mitochondrial_myopathy|not_provided|Mitochondrial_myopathy|_episodic|_with_optic_atrophy_and_reversible_leukoencephalopathy": 1,
    "Immunodeficiency_35": 711,
    "not_provided|Immunodeficiency_35": 30,
    "Immunodeficiency_35|not_provided": 11,
    "not_specified|not_provided|Immunodeficiency_35": 8,
    "Inborn_genetic_diseases|Immunodeficiency_35": 24,
    "not_provided|not_specified|Immunodeficiency_35": 3,
    "Immunodeficiency_35|not_specified|not_provided": 4,
    "TYK2-related_disorder": 2,
    "Immunodeficiency_35|not_specified": 8,
    "Immunodeficiency_35|TYK2-related_disorder": 6,
    "Immunodeficiency_35|Inborn_genetic_diseases": 22,
    "Immunodeficiency_35|TYK2-related_disorder|not_provided": 1,
    "not_specified|Immunodeficiency_35": 10,
    "TYK2-related_disorder|Immunodeficiency_35": 9,
    "Immunodeficiency_35|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|Immunodeficiency_35|not_provided": 2,
    "not_provided|Immunodeficiency_35|not_specified": 4,
    "Recurrent_skin_infections|Immunodeficiency": 1,
    "TYK2-related_disorder|not_provided|Immunodeficiency_35": 1,
    "not_provided|Immunodeficiency_35|TYK2-related_disorder": 1,
    "not_provided|Immunodeficiency_35|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Immunodeficiency_35": 2,
    "not_provided|Recurrent_skin_infections|Immunodeficiency|Immunodeficiency_35": 1,
    "not_provided|Inborn_genetic_diseases|Immunodeficiency_35": 1,
    "Virus-induced_diabetes|Immunodeficiency_35": 3,
    "Virus-induced_diabetes": 3,
    "SPERMATOGENIC_FAILURE_101": 5,
    "ATG4D-related_neurodevelopmental_condition|Neurodevelopmental_disorder|not_specified|ASHER": 1,
    "ATG4D-related_neurodevelopmental_condition|not_provided|ASHER": 1,
    "ASHER": 1,
    "Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 24,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 25,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases": 2,
    "Centronuclear_myopathy|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 47,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 7,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 25,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided": 43,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 6,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 12,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 15,
    "DNM2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Centronuclear_myopathy|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases": 20,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified": 4,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|Autosomal_dominant_centronuclear_myopathy|Peripheral_neuropathy": 1,
    "Autosomal_dominant_centronuclear_myopathy|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|not_provided|DNM2-related_disorder": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|not_provided": 1,
    "not_specified|Centronuclear_myopathy|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 1,
    "not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|not_specified": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|DNM2-related_disorder|Autosomal_dominant_centronuclear_myopathy|not_provided|not_specified": 1,
    "DNM2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 1,
    "DNM2-related_disorder|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|not_provided": 8,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|DNM2-related_disorder": 3,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided": 6,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 3,
    "not_specified|Inborn_genetic_diseases|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Autosomal_dominant_centronuclear_myopathy|not_provided": 1,
    "not_provided|DNM2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|DNM2-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 1,
    "DNM2-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 2,
    "DNM2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "not_specified|not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases": 1,
    "DNM2-related_disorder|not_provided|not_specified|Centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|DNM2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Centronuclear_myopathy|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 2,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 3,
    "DNM2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|not_specified|Centronuclear_Myopathy|_Dominant|Charcot-Marie-Tooth|_Intermediate|not_provided": 1,
    "Autosomal_dominant_centronuclear_myopathy|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Inborn_genetic_diseases|not_specified|Centronuclear_myopathy|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified": 10,
    "Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Myofibrillar_myopathy|Limb-girdle_muscle_weakness": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "DNM2-related_disorder": 4,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2M|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_specified|not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "DNM2-related_disorder|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Myopathy|Centronuclear_myopathy": 1,
    "Charcot-Marie-Tooth_disease|Limb-girdle_muscular_dystrophy|not_provided|Centronuclear_myopathy|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Centronuclear_myopathy": 1,
    "Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases": 3,
    "not_provided|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided": 2,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Charcot-Marie-Tooth_disease": 2,
    "not_specified|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|DNM2-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Inborn_genetic_diseases|not_provided": 2,
    "DNM2-related_disorder|Centronuclear_myopathy|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Abnormality_of_the_musculature": 1,
    "not_provided|Inborn_genetic_diseases|DNM2-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|Autosomal_dominant_centronuclear_myopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 4,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|not_provided": 1,
    "DNM2-related_disorder|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 2,
    "Autosomal_dominant_centronuclear_myopathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified|not_provided": 3,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|not_specified": 2,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Centronuclear_myopathy": 1,
    "Centronuclear_myopathy|not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|See_cases": 1,
    "Centronuclear_myopathy|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Sensorimotor_neuropathy": 1,
    "Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2M|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|Centronuclear_myopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Charcot-Marie-Tooth_disease|_dominant_intermediate_B|_with_neutropenia|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|_dominant_intermediate_B|_with_neutropenia|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Charcot-Marie-Tooth_disease": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|DNM2-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified|not_provided": 1,
    "Centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 2,
    "Centronuclear_myopathy|Inborn_genetic_diseases|not_specified|DNM2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Centronuclear_myopathy|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided": 1,
    "not_provided|Severe_X-linked_myotubular_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Severe_X-linked_myotubular_myopathy|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Centronuclear_myopathy|not_provided": 1,
    "Centronuclear_myopathy|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_provided|Centronuclear_myopathy|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|Centronuclear_myopathy": 1,
    "not_provided|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_specified|Inborn_genetic_diseases": 1,
    "DNM2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|Centronuclear_myopathy|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|not_specified|not_provided": 1,
    "Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|DNM2-related_disorder|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy|not_specified|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|Autosomal_dominant_Charcot-Marie-Tooth_disease_type_2M": 1,
    "Autosomal_dominant_centronuclear_myopathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Centronuclear_myopathy": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_specified|Centronuclear_myopathy|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|not_provided": 1,
    "DNM2-related_disorder|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Fetal_akinesia-cerebral_and_retinal_hemorrhage_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_centronuclear_myopathy|Charcot-Marie-Tooth_disease_dominant_intermediate_B": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_dominant_intermediate_B|Autosomal_dominant_centronuclear_myopathy": 1,
    "Centronuclear_Myopathy|_Dominant|Charcot-Marie-Tooth|_Intermediate": 2,
    "Coffin-Siris_syndrome|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2": 2337,
    "Neurodevelopmental_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "not_specified|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 47,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 773,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 726,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided": 22,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16": 63,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 54,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 29,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 14,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome": 26,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 7,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 53,
    "Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 27,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|SMARCA4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided": 5,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder": 5,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 41,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 30,
    "Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided": 5,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 7,
    "Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 11,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 14,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 32,
    "Hereditary_cancer-predisposing_syndrome|not_provided|SMARCA4-related_disorder|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 2,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 30,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 2,
    "Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_16|not_specified|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified": 6,
    "Coffin-Siris_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 8,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16": 6,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided": 19,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 6,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_specified|not_provided": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 1,
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    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16": 11,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided": 9,
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    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
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    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16": 4,
    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|bilateral_breast_cancer": 1,
    "not_provided|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Hereditary_cancer-predisposing_syndrome": 3,
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    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
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    "Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 4,
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    "Intellectual_disability|_autosomal_dominant_16": 26,
    "Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
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    "not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 6,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 6,
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    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder|Coffin-Siris_syndrome": 1,
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    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16": 11,
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    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 5,
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    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|Hereditary_cancer-predisposing_syndrome": 2,
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    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_specified": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 10,
    "Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 1,
    "Otosclerosis_12|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|Coffin-Siris_syndrome|not_provided|not_specified": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 8,
    "not_provided|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 34,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 7,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 6,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_nonpolyposis_colon_cancer|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
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    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|SMARCA4-related_disorder": 2,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified": 7,
    "SMARCA4-related_disorder": 13,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_specified|Coffin-Siris_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder|Intellectual_disability|not_provided": 1,
    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 7,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|SMARCA4-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 3,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_specified": 1,
    "SMARCA4-related_disorder|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 2,
    "Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_16": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Neurodevelopmental_disorder": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome": 1,
    "SMARCA4-related_disorder|Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_specified|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|Coffin-Siris_syndrome": 1,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Coffin-Siris_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 3,
    "SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided": 3,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|SMARCA4-related_disorder": 2,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 5,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_BAFopathy|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Ventricular_septal_defect|Facial_asymmetry|Strabismus|Single_transverse_palmar_crease|Global_developmental_delay|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_specified|not_provided|Otosclerosis_12|Coffin-Siris_syndrome": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|SMARCA4-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Coffin-Siris_syndrome": 1,
    "Hereditary_nonpolyposis_colon_cancer|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
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    "Intellectual_disability|Autistic_behavior": 3,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided|SMARCA4-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_specified|Otosclerosis_12|Coffin-Siris_syndrome|not_provided": 1,
    "not_specified|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 2,
    "SMARCA4-related_disorder|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 4,
    "Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_16|not_provided": 5,
    "Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_BAFopathy": 2,
    "SMARCA4-related_BAFopathy": 4,
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    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|See_cases|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Otosclerosis_12": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Intellectual_disability|_autosomal_dominant_16": 3,
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    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Otosclerosis_12": 1,
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    "not_provided|SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCA4-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
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    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 4,
    "not_provided|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|not_specified": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_specified|not_provided": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder": 1,
    "Coffin-Siris_syndrome|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Microcephaly": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16": 2,
    "SMARCA4-related_disorder|not_specified|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_16|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "SMARCA4-related_disorder|Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|Coffin-Siris_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_nonpolyposis_colon_cancer": 1,
    "Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|Coffin-Siris_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 3,
    "Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_16|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 2,
    "Coffin-Siris_syndrome|Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "SMARCA4-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_specified": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome": 1,
    "Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_16|not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Intellectual_disability|_autosomal_dominant_16|not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_16|Intellectual_disability": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder": 1,
    "Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 2,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_16": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_autosomal_dominant_16": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_BAFopathy|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "SMARCA4-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_BAFopathy": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Medulloblastoma": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|SMARCA4-related_disorder": 1,
    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 2,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16": 2,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Coffin-Siris_syndrome|Intellectual_disability|_autosomal_dominant_16": 1,
    "Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "not_specified|SMARCA4-related_disorder": 1,
    "SMARCA4-related_disorder|Atrial_septal_defect|Ventricular_septal_defect|Delayed_speech_and_language_development|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|SMARCA4-related_disorder": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|SMARCA4-related_BAFopathy|Cleft_palate|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder": 1,
    "not_specified|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|not_provided": 1,
    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "SMARCA4-related_disorder|Coffin-Siris_syndrome|Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Coffin-Siris_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_16|Inborn_genetic_diseases|Intellectual_disability|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Intellectual_disability|_autosomal_dominant_16": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|Cerebral_palsy": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Intellectual_disability|_autosomal_dominant_16|not_provided": 2,
    "Hereditary_nonpolyposis_colon_cancer|Malignant_tumor_of_breast|not_specified|not_provided|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16": 1,
    "SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCA4-related_BAFopathy|not_provided|Intellectual_disability|_autosomal_dominant_16": 1,
    "SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2": 2,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Coffin-Siris_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_16": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|not_specified": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "SMARCA4-related_disorder|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|SMARCA4-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Seizure": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|not_provided|SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "See_cases|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Intellectual_disability|_autosomal_dominant_16|not_specified|Coffin-Siris_syndrome": 1,
    "Coffin-Siris_syndrome|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Ovarian_neoplasm": 1,
    "not_provided|not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Coffin-Siris_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Obesity|intellectual_deficiency|Coffin-Siris_syndrome|not_provided": 1,
    "Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|not_specified": 1,
    "SMARCA4-related_disorder|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder": 1,
    "Small_cell_carcinoma_of_the_ovary|_hypercalcemic_type|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Intellectual_disability|_autosomal_dominant_16|not_provided|Rhabdoid_tumor_predisposition_syndrome_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|not_specified|Otosclerosis_12|Coffin-Siris_syndrome": 1,
    "Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Otosclerosis_12": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome|Small_cell_carcinoma_of_the_ovary|_hypercalcemic_type|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Small_cell_carcinoma_of_the_ovary|_hypercalcemic_type|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|SMARCA4-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16": 1,
    "not_specified|not_provided|Hereditary_nonpolyposis_colon_cancer|Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Intellectual_disability|_autosomal_dominant_16|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Otosclerosis_12|Hereditary_cancer-predisposing_syndrome|not_provided|SMARCA4-related_disorder": 1,
    "SMARCA4-related_disorder|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|SMARCA4-related_disorder|Otosclerosis_12": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided|SMARCA4-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|SMARCA4-related_disorder|not_specified|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Coffin-Siris_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_16|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|Hereditary_cancer-predisposing_syndrome|SMARCA4-related_disorder": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Coffin-Siris_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|SMARCA4-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_16|Rhabdoid_tumor_predisposition_syndrome_2|Hereditary_cancer-predisposing_syndrome|Diffuse_midline_glioma|_H3_K27-altered": 1,
    "not_provided|SMARCA4-related_disorder|Rhabdoid_tumor_predisposition_syndrome_2": 1,
    "Otosclerosis_12|Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_16|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_specified|not_provided": 1,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 85,
    "Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia": 36,
    "LDLR-related_disorder|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 6,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 119,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 167,
    "Familial_hypercholesterolemia|LDLR-related_disorder": 1,
    "LDLR-related_disorder|Hypercholesterolemia|_familial|_1": 3,
    "not_provided|Hypercholesterolemia|_familial|_1|not_specified": 1,
    "LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 6,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 25,
    "Early-onset_coronary_artery_disease|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 11,
    "Homozygous_familial_hypercholesterolemia": 5,
    "Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia": 3,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia": 7,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 17,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 39,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia": 6,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1": 10,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Smith-Lemli-Opitz_syndrome": 2,
    "not_provided|not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 12,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_specified": 2,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 22,
    "Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 3,
    "Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 6,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 14,
    "Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|not_provided|LDLR-related_disorder|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_familial|_1": 6,
    "not_specified|Familial_hypercholesterolemia": 7,
    "LDLR-related_disorder|Familial_hypercholesterolemia": 4,
    "Dyslipidemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 10,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 5,
    "Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 2,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Early-onset_coronary_artery_disease": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 2,
    "Hypercholesterolemia|_familial|_1|Dyslipidemia": 3,
    "not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia": 2,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 35,
    "Dyslipidemia|Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 2,
    "Dyslipidemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 3,
    "Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 5,
    "Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 3,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 4,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 8,
    "Familial_hypercholesterolemia|not_provided|LDLR-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Dyslipidemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "LDLR-related_disorder|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 3,
    "not_provided|LDLR-related_disorder": 1,
    "not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "LDLR-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided|not_specified": 1,
    "Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "not_provided|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 5,
    "Cardiovascular_phenotype|Dyslipidemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 3,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided": 5,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 5,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "LDLR-related_disorder": 6,
    "LDLR-related_disorder|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Dyslipidemia|Hypercholesterolemia|_familial|_1": 7,
    "Dyslipidemia": 5,
    "not_provided|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 5,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype": 3,
    "Dyslipidemia|Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "Homozygous_familial_hypercholesterolemia|LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 2,
    "Cardiovascular_phenotype|LDLR-related_disorder|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Familial_hypercholesterolemia": 3,
    "Cardiovascular_phenotype|Dyslipidemia|not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 3,
    "Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 3,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 6,
    "Hypercholesterolemia|_familial|_1|not_provided|not_specified": 1,
    "Dyslipidemia|LDLR-related_disorder|Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 4,
    "LDLR-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Homozygous_familial_hypercholesterolemia|not_provided|Familial_hypercholesterolemia": 1,
    "Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype": 1,
    "Dyslipidemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype": 1,
    "Dyslipidemia|Cardiovascular_phenotype|not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 3,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|not_provided": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Familial_hypercholesterolemia|not_provided": 2,
    "not_specified|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 8,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 2,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 5,
    "Familial_hypercholesterolemia|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided|Hypercholesterolemia|See_cases": 1,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 3,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia": 2,
    "Dyslipidemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 4,
    "not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 2,
    "LDLR-related_disorder|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 2,
    "Cardiovascular_phenotype|Dyslipidemia|LDLR-related_disorder|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 5,
    "Dyslipidemia|Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype": 2,
    "Dyslipidemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "not_specified|Hypercholesterolemia|_familial|_1|not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Cowden_syndrome_1": 1,
    "Familial_hypercholesterolemia|Familial_type_3_hyperlipoproteinemia|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "not_specified|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|Dyslipidemia|not_provided": 1,
    "LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia|_autosomal_dominant|_type_B|See_cases": 1,
    "Dyslipidemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 3,
    "Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dyslipidemia|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Hyperlipidemia|not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Dyslipidemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_specified|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|not_provided": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Dyslipidemia|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Autosomal_dominant_familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Dyslipidemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 2,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Homozygous_familial_hypercholesterolemia|Hypercholesterolemia|_familial|_4|Familial_hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_4|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Dyslipidemia|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_specified": 2,
    "Homozygous_familial_hypercholesterolemia|Dyslipidemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 3,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Dyslipidemia": 1,
    "Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 2,
    "not_provided|Hypercholesterolemia|_familial|_1|LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Cardiovascular_phenotype|Dyslipidemia|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases|Hypercholesterolemia": 1,
    "not_specified|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_1|Dyslipidemia|not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Dyslipidemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Dyslipidemia|LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|not_specified|LDLR-related_disorder|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|not_provided": 1,
    "LDLR-related_disorder|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Dyslipidemia|Cardiovascular_phenotype|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Homozygous_familial_hypercholesterolemia|LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|LDLR-related_disorder": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|LDLR-related_disorder|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "See_cases|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Hypercholesterolemia|_familial|_1|LDLR-related_disorder": 3,
    "Dyslipidemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Familial_hypercholesterolemia|LDLR-related_disorder|not_provided|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|Syndromic_X-linked_intellectual_disability_Najm_type|See_cases|Hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Dyslipidemia|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|LDLR-related_disorder|Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "Homozygous_familial_hypercholesterolemia|not_provided|Familial_hypercholesterolemia": 1,
    "not_specified|Familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_provided|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|LDLR-related_disorder|Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypercholesterolemia|_familial|_1|Homozygous_familial_hypercholesterolemia|Familial_hypercholesterolemia": 1,
    "not_provided|not_specified|Hypercholesterolemia|_familial|_1": 2,
    "not_provided|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype": 1,
    "Dyslipidemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1|See_cases": 1,
    "Dyslipidemia|Familial_hypercholesterolemia|not_provided": 1,
    "Homozygous_familial_hypercholesterolemia|Dyslipidemia|LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_provided|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Dyslipidemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|LDLR-related_disorder|not_provided|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Dyslipidemia|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|Dyslipidemia|not_provided|LDLR-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Familial_hypercholesterolemia|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia": 1,
    "not_specified|Cardiovascular_phenotype|Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Hypercholesterolemia|_familial|_1|Familial_type_3_hyperlipoproteinemia": 1,
    "Familial_hypercholesterolemia|Homozygous_familial_hypercholesterolemia": 1,
    "Cardiovascular_phenotype|Familial_hypercholesterolemia|Dyslipidemia": 1,
    "Familial_hypercholesterolemia|not_provided|not_specified|LDLR-related_disorder|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Familial_hypercholesterolemia|Dyslipidemia|Homozygous_familial_hypercholesterolemia|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "not_provided|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia|Cardiovascular_phenotype": 1,
    "not_specified|Hypercholesterolemia|_familial|_1|Familial_hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|Cardiovascular_phenotype|not_provided|not_specified|Hypercholesterolemia|_familial|_1": 1,
    "Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|Familial_hypercholesterolemia|LDLR-related_disorder": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|Cardiovascular_phenotype|not_provided|LDLR-related_disorder|Homozygous_familial_hypercholesterolemia": 1,
    "Dyslipidemia|LDLR-related_disorder|Cardiovascular_phenotype|Familial_hypercholesterolemia|not_specified|not_provided|Hypercholesterolemia|_familial|_1|Hypercholesterolemia": 1,
    "not_provided|Familial_hypercholesterolemia|not_specified|Cardiovascular_phenotype|Hypercholesterolemia|_familial|_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Familial_hypercholesterolemia": 1,
    "Familial_hypercholesterolemia|Hypercholesterolemia|_familial|_1|not_specified|not_provided": 1,
    "Familial_hypercholesterolemia|not_specified|Hypercholesterolemia|_familial|_1|not_provided": 1,
    "Hypercholesterolemia|_familial|_1|not_provided|Familial_hypercholesterolemia": 2,
    "SPC24-related_disorder": 1,
    "not_provided|not_specified|Nephrotic_syndrome_16|Wooly_hair-palmoplantar_keratoderma_syndrome": 1,
    "not_provided|KANK2-related_disorder": 8,
    "KANK2-related_disorder": 11,
    "not_provided|Nephrotic_syndrome_16|Wooly_hair-palmoplantar_keratoderma_syndrome": 1,
    "KANK2-related_disorder|not_provided": 12,
    "Wooly_hair-palmoplantar_keratoderma_syndrome|Nephrotic_syndrome_16": 2,
    "Nephrotic_syndrome_16|not_provided": 1,
    "Nephrotic_syndrome_16": 2,
    "Wooly_hair-palmoplantar_keratoderma_syndrome": 1,
    "not_specified|KANK2-related_disorder|not_provided": 1,
    "Nephrotic_syndrome_16|Wooly_hair-palmoplantar_keratoderma_syndrome|not_provided": 3,
    "Nephrotic_syndrome_16|Wooly_hair-palmoplantar_keratoderma_syndrome|KANK2-related_disorder|not_provided|not_specified": 1,
    "KANK2-related_disorder|Nephrotic_syndrome_16|Wooly_hair-palmoplantar_keratoderma_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Adams-Oliver_syndrome_2|not_provided": 2,
    "not_provided|Adams-Oliver_syndrome_2": 7,
    "Adams-Oliver_syndrome_2": 36,
    "not_provided|DOCK6-related_disorder": 23,
    "DOCK6-related_disorder|not_provided": 29,
    "Inborn_genetic_diseases|not_provided|Adams-Oliver_syndrome_2|DOCK6-related_disorder": 1,
    "DOCK6-related_disorder": 20,
    "not_provided|not_specified|Adams-Oliver_syndrome_2": 2,
    "not_provided|Adams-Oliver_syndrome_2|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|Adams-Oliver_syndrome_2": 1,
    "DOCK6-related_disorder|not_provided|not_specified": 2,
    "Adams-Oliver_syndrome_2|not_specified|not_provided": 2,
    "not_provided|Adams-Oliver_syndrome_2|not_specified": 3,
    "Adams-Oliver_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "Adams-Oliver_syndrome|not_provided|Adams-Oliver_syndrome_2": 1,
    "DOCK6-related_disorder|Inborn_genetic_diseases|not_provided": 5,
    "not_specified|not_provided|DOCK6-related_disorder|Adams-Oliver_syndrome_2": 1,
    "Adams-Oliver_syndrome_2|not_provided": 7,
    "DOCK6-related_disorder|not_provided|Adams-Oliver_syndrome_2|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Adams-Oliver_syndrome_2": 2,
    "Inborn_genetic_diseases|not_provided|Adams-Oliver_syndrome_2": 3,
    "DOCK6-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Adams-Oliver_syndrome_1|DOCK6-related_disorder": 1,
    "not_specified|Adams-Oliver_syndrome_2|not_provided": 3,
    "DOCK6-related_disorder|not_provided|Adams-Oliver_syndrome_2": 2,
    "Adams-Oliver_syndrome_2|DOCK6-related_disorder": 1,
    "not_provided|DOCK6-related_disorder|Inborn_genetic_diseases": 2,
    "DOCK6-related_disorder|Adams-Oliver_syndrome_2": 1,
    "Adams-Oliver_syndrome_2|DOCK6-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Adams-Oliver_syndrome_2|DOCK6-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|DOCK6-related_disorder": 2,
    "Inborn_genetic_diseases|DOCK6-related_disorder|not_provided": 2,
    "Adams-Oliver_syndrome_2|not_provided|DOCK6-related_disorder": 1,
    "Inborn_genetic_diseases|Adams-Oliver_syndrome_2": 2,
    "Inborn_genetic_diseases|Adams-Oliver_syndrome_2|Adams-Oliver_syndrome": 1,
    "Adams-Oliver_syndrome_2|Inborn_genetic_diseases": 1,
    "Hydrocephalus|_nonsyndromic|_autosomal_recessive_1|Macrocephaly": 1,
    "Adams-Oliver_syndrome_2|not_provided|not_specified": 1,
    "Adams-Oliver_syndrome_2|Adams-Oliver_syndrome|not_provided": 1,
    "DOCK6-related_disorder|not_specified|not_provided": 1,
    "DOCK6-related_disorder|not_provided|Intellectual_disability|Bone_Paget_disease": 1,
    "not_provided|Adams-Oliver_syndrome_2|DOCK6-related_disorder|Inborn_genetic_diseases": 1,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation|not_provided": 7,
    "not_provided|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Primary_familial_polycythemia_due_to_EPO_receptor_mutation": 1,
    "not_specified|not_provided|Primary_familial_polycythemia_due_to_EPO_receptor_mutation": 2,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_familial_polycythemia_due_to_EPO_receptor_mutation": 1,
    "not_provided|Primary_familial_polycythemia_due_to_EPO_receptor_mutation": 5,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation|Acute_megakaryoblastic_leukemia_without_down_syndrome": 1,
    "not_specified|Primary_familial_polycythemia_due_to_EPO_receptor_mutation|not_provided": 1,
    "EPOR-related_disorder": 1,
    "Primary_familial_polycythemia_due_to_EPO_receptor_mutation|EPOR-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Primary_familial_polycythemia_due_to_EPO_receptor_mutation": 2,
    "Primary_ciliary_dyskinesia_30": 241,
    "Primary_ciliary_dyskinesia_30|ODAD3-related_disorder": 5,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_30": 15,
    "Primary_ciliary_dyskinesia_30|Inborn_genetic_diseases": 11,
    "Primary_ciliary_dyskinesia_30|not_specified": 1,
    "ODAD3-related_disorder|Primary_ciliary_dyskinesia_30": 2,
    "not_provided|Primary_ciliary_dyskinesia_30": 6,
    "Primary_ciliary_dyskinesia_30|not_provided": 9,
    "Primary_ciliary_dyskinesia_30|Kartagener_syndrome": 2,
    "ODAD3-related_disorder": 3,
    "Primary_ciliary_dyskinesia_30|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia_30|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_30": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_30|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Primary_ciliary_dyskinesia_30": 2,
    "ODAD3-related_disorder|not_provided|Primary_ciliary_dyskinesia_30": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia_30": 1,
    "not_provided|Inborn_genetic_diseases|Primary_ciliary_dyskinesia_30": 1,
    "Primary_ciliary_dyskinesia_30|not_specified|not_provided": 1,
    "not_provided|Polycystic_liver_disease_1": 17,
    "Primary_ciliary_dyskinesia_30|ODAD3-related_disorder|not_provided": 1,
    "not_specified|Polycystic_liver_disease_1|not_provided": 1,
    "Polycystic_liver_disease_1|Inborn_genetic_diseases|not_provided": 5,
    "Polycystic_liver_disease_1|not_provided|Inborn_genetic_diseases": 3,
    "PRKCSH-related_disorder": 1,
    "not_provided|Polycystic_liver_disease_1|Inborn_genetic_diseases": 5,
    "not_provided|PRKCSH-related_disorder|Inborn_genetic_diseases|Polycystic_liver_disease_1": 1,
    "not_provided|Polycystic_liver_disease_1|PRKCSH-related_disorder": 1,
    "Polycystic_liver_disease_1|not_provided|not_specified": 2,
    "not_specified|not_provided|Polycystic_liver_disease_1": 3,
    "Polycystic_liver_disease_1|Autosomal_dominant_polycystic_liver_disease|PRKCSH-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Polycystic_liver_disease_1": 3,
    "Polycystic_liver_disease_1|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Polycystic_liver_disease_1|not_provided": 2,
    "PRKCSH-related_disorder|Polycystic_liver_disease_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_liver_disease_1": 1,
    "PRKCSH-related_disorder|not_provided": 2,
    "Polycystic_liver_disease_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Polycystic_liver_disease_1|Autosomal_dominant_polycystic_liver_disease": 1,
    "not_provided|PRKCSH-related_disorder": 3,
    "PRKCSH-related_disorder|Polycystic_liver_disease_1|not_provided": 1,
    "not_provided|not_specified|Polycystic_liver_disease_1": 1,
    "Inborn_genetic_diseases|not_provided|Polycystic_liver_disease_1|Autosomal_dominant_polycystic_liver_disease": 1,
    "not_provided|Inborn_genetic_diseases|Polycystic_liver_disease_1": 1,
    "See_cases|Polycystic_liver_disease_1": 1,
    "Polycystic_liver_disease_1|not_specified|not_provided": 1,
    "Spondyloenchondrodysplasia_with_immune_dysregulation": 241,
    "Inborn_genetic_diseases|Spondyloenchondrodysplasia_with_immune_dysregulation": 16,
    "Spondyloenchondrodysplasia_with_immune_dysregulation|not_provided": 9,
    "Spondyloenchondrodysplasia_with_immune_dysregulation|ACP5-related_disorder": 3,
    "Spondyloenchondrodysplasia_with_immune_dysregulation|Inborn_genetic_diseases": 9,
    "not_provided|Spondyloenchondrodysplasia_with_immune_dysregulation": 7,
    "ACP5-related_disorder|Spondyloenchondrodysplasia_with_immune_dysregulation": 1,
    "ACP5-related_disorder|not_specified|not_provided|Spondyloenchondrodysplasia_with_immune_dysregulation": 1,
    "Spondyloenchondrodysplasia_with_immune_dysregulation|not_specified|not_provided": 1,
    "not_provided|Spondyloenchondrodysplasia_with_immune_dysregulation|not_specified": 2,
    "not_specified|Spondyloenchondrodysplasia_with_immune_dysregulation|not_provided": 1,
    "not_specified|Spondyloenchondrodysplasia_with_immune_dysregulation": 1,
    "Inborn_genetic_diseases|Spondyloenchondrodysplasia_with_immune_dysregulation|ACP5-related_disorder": 1,
    "Inborn_genetic_diseases|Spondyloenchondrodysplasia_with_immune_dysregulation|not_provided": 1,
    "ACP5-related_disorder|Spondyloenchondrodysplasia_with_immune_dysregulation|not_provided|not_specified": 1,
    "Spondyloenchondrodysplasia_with_immune_dysregulation|not_specified": 1,
    "Deficiency_of_alpha-mannosidase": 1521,
    "not_provided|Deficiency_of_alpha-mannosidase": 53,
    "Deficiency_of_alpha-mannosidase|Inborn_genetic_diseases": 39,
    "Deficiency_of_alpha-mannosidase|Inborn_genetic_diseases|not_provided": 1,
    "Deficiency_of_alpha-mannosidase|not_specified": 9,
    "Deficiency_of_alpha-mannosidase|MAN2B1-related_disorder": 6,
    "not_provided|not_specified|Deficiency_of_alpha-mannosidase": 2,
    "not_provided|Deficiency_of_alpha-mannosidase|Inborn_genetic_diseases": 3,
    "MAN2B1-related_disorder|Deficiency_of_alpha-mannosidase": 4,
    "Inborn_genetic_diseases|Deficiency_of_alpha-mannosidase": 17,
    "MAN2B1-related_disorder|not_specified|Deficiency_of_alpha-mannosidase": 2,
    "Deficiency_of_alpha-mannosidase|not_provided": 17,
    "not_provided|Inborn_genetic_diseases|Deficiency_of_alpha-mannosidase": 2,
    "not_specified|Deficiency_of_alpha-mannosidase": 9,
    "MAN2B1-related_disorder|not_provided|Deficiency_of_alpha-mannosidase": 7,
    "not_provided|Deficiency_of_alpha-mannosidase|not_specified": 1,
    "Inborn_genetic_diseases|Deficiency_of_alpha-mannosidase|MAN2B1-related_disorder": 1,
    "Deficiency_of_alpha-mannosidase|Mannosidosis|_alpha-|_types_I_and_II": 1,
    "Deficiency_of_alpha-mannosidase|Mannosidosis|_alpha-|_types_I_and_II|not_provided": 1,
    "not_specified|not_provided|Deficiency_of_alpha-mannosidase": 11,
    "not_specified|not_provided|Deficiency_of_alpha-mannosidase|MAN2B1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_alpha-mannosidase": 5,
    "not_provided|Deficiency_of_alpha-mannosidase|Intellectual_disability": 1,
    "Deficiency_of_alpha-mannosidase|Intellectual_disability|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Mannosidosis|_alpha-|_types_I_and_II": 1,
    "Inborn_genetic_diseases|Deficiency_of_alpha-mannosidase|not_provided": 1,
    "Deficiency_of_alpha-mannosidase|MAN2B1-related_disorder|not_provided": 1,
    "Deficiency_of_alpha-mannosidase|not_specified|MAN2B1-related_disorder": 1,
    "Deficiency_of_alpha-mannosidase|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Deficiency_of_alpha-mannosidase|not_provided": 1,
    "MAN2B1-related_disorder": 2,
    "Deficiency_of_alpha-mannosidase|Intellectual_disability": 1,
    "not_provided|Deficiency_of_alpha-mannosidase|MAN2B1-related_disorder|not_specified": 2,
    "not_provided|Deficiency_of_alpha-mannosidase|Intellectual_disability|MAN2B1-related_disorder": 1,
    "MAN2B1-related_disorder|not_specified|not_provided|Deficiency_of_alpha-mannosidase": 1,
    "Craniosynostosis_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Deficiency_of_alpha-mannosidase": 1,
    "not_provided|Hypercholanemia|_familial": 1,
    "Hypercholanemia|_familial|Neurodevelopmental_disorder_with_variable_familial_hypercholanemia": 2,
    "Neurodevelopmental_disorder_with_seizures_and_speech_and_walking_impairment|not_provided|Hypercholanemia|_familial": 1,
    "Neurodevelopmental_disorder_with_variable_familial_hypercholanemia": 1,
    "not_provided|Neurodevelopmental_disorder_with_seizures_and_speech_and_walking_impairment": 1,
    "not_provided|Neurodevelopmental_disorder_with_seizures_and_speech_and_walking_impairment|DHPS-related_disorder": 1,
    "DHPS-related_disorder|not_provided": 1,
    "DHPS-related_disorder": 6,
    "DHPS-related_disorder|Neurodevelopmental_disorder_with_seizures_and_speech_and_walking_impairment|not_provided": 1,
    "Neurodevelopmental_disorder_with_seizures_and_speech_and_walking_impairment|not_provided": 2,
    "not_provided|DHPS-related_disorder": 1,
    "TNPO2-related_disorder": 9,
    "Intellectual_developmental_disorder_with_hypotonia|_impaired_speech|_and_dysmorphic_facies": 17,
    "Intellectual_developmental_disorder_with_hypotonia|_impaired_speech|_and_dysmorphic_facies|not_provided": 1,
    "TNPO2-related_disorder|Intellectual_developmental_disorder_with_hypotonia|_impaired_speech|_and_dysmorphic_facies": 2,
    "Inborn_genetic_diseases|TNPO2-related_disorder": 1,
    "Cardiomyopathy|_dilated|_2H": 1,
    "Aicardi-Goutieres_syndrome_4": 419,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_4": 2,
    "not_provided|Aicardi-Goutieres_syndrome_4|not_specified": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_4": 12,
    "not_specified|not_provided|Aicardi-Goutieres_syndrome_4": 2,
    "not_provided|Aicardi-Goutieres_syndrome_4": 10,
    "RNASEH2A-related_disorder|Aicardi-Goutieres_syndrome_4": 3,
    "Aicardi-Goutieres_syndrome_4|Inborn_genetic_diseases": 10,
    "Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_4": 2,
    "Aicardi-Goutieres_syndrome_4|Inborn_genetic_diseases|not_provided": 1,
    "Aicardi-Goutieres_syndrome_4|not_provided": 4,
    "Aicardi-Goutieres_syndrome_4|RNASEH2A-related_disorder": 3,
    "not_provided|RNASEH2A-related_type_1_interferonopathy|RNASEH2A-related_disorder|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_4": 1,
    "RNASEH2A-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_4": 2,
    "not_specified|Aicardi-Goutieres_syndrome_4": 2,
    "Aicardi-Goutieres_syndrome_4|not_specified": 2,
    "not_provided|not_specified|Aicardi-Goutieres_syndrome_4": 4,
    "RNASEH2A-related_disorder|Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_4": 1,
    "Aicardi-Goutieres_syndrome_4|Aicardi_Goutieres_syndrome|RNASEH2A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RNASEH2A-related_disorder|not_provided|Aicardi-Goutieres_syndrome_4|not_specified": 1,
    "not_specified|not_provided|RNASEH2A-related_disorder|Aicardi-Goutieres_syndrome_4": 1,
    "Aicardi-Goutieres_syndrome_4|not_provided|not_specified": 1,
    "not_provided|Aicardi-Goutieres_syndrome_4|RNASEH2A-related_disorder": 1,
    "Aicardi-Goutieres_syndrome_4|RNASEH2A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Aicardi-Goutieres_syndrome_4|Inborn_genetic_diseases": 1,
    "MAST1-related_disorder": 12,
    "Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations|not_provided": 1,
    "Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations": 34,
    "not_provided|Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations": 4,
    "not_provided|MAST1-related_disorder": 14,
    "MAST1-related_disorder|not_provided": 9,
    "Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations|Inborn_genetic_diseases": 1,
    "MAST1-related_disorder|Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations|not_provided": 1,
    "not_provided|MAST1-related_disorder|Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations": 1,
    "MAST1-related_disorder|See_cases|not_provided": 1,
    "Mega-corpus-callosum_syndrome_with_cerebellar_hypoplasia_and_cortical_malformations|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|MAST1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|DNASE2-related_disorder|not_provided": 1,
    "not_provided|Autoinflammatory-pancytopenia_syndrome_due_to_DNASE2_deficiency": 1,
    "DNASE2-related_disorder|not_provided": 1,
    "DNASE2-related_disorder": 3,
    "Autoinflammatory-pancytopenia_syndrome_due_to_DNASE2_deficiency": 4,
    "Congenital_dyserythropoietic_anemia_type_4": 18,
    "Congenital_dyserythropoietic_anemia_type_4|not_provided": 9,
    "not_provided|BLOOD_GROUP--LUTHERAN_INHIBITOR|Congenital_dyserythropoietic_anemia_type_4": 1,
    "BLOOD_GROUP--LUTHERAN_INHIBITOR": 6,
    "not_provided|Inborn_genetic_diseases|KLF1-related_disorder": 1,
    "FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6|Congenital_dyserythropoietic_anemia_type_4|BLOOD_GROUP--LUTHERAN_INHIBITOR": 1,
    "Anemia|_congenital_dyserythropoietic|_type_IVb": 2,
    "BLOOD_GROUP--LUTHERAN_INHIBITOR|not_provided": 3,
    "not_provided|Congenital_dyserythropoietic_anemia_type_4|BLOOD_GROUP--LUTHERAN_INHIBITOR": 1,
    "KLF1-related_disorder|Anemia|_congenital_dyserythropoietic|_type_IVb|FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6|BLOOD_GROUP--LUTHERAN_INHIBITOR": 1,
    "not_specified|not_provided|BLOOD_GROUP--LUTHERAN_INHIBITOR": 1,
    "KLF1-related_disorder": 7,
    "not_provided|Congenital_dyserythropoietic_anemia_type_4": 5,
    "Anemia|_congenital_dyserythropoietic|_type_IVb|FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6": 1,
    "Anemia|_congenital_dyserythropoietic|_type_IVb|BLOOD_GROUP--LUTHERAN_INHIBITOR|FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6|Congenital_dyserythropoietic_anemia_type_4|not_provided": 1,
    "FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6": 1,
    "KLF1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_dyserythropoietic_anemia_type_4": 1,
    "BLOOD_GROUP--LUTHERAN_INHIBITOR|not_provided|Anemia|_congenital_dyserythropoietic|_type_IVb|FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6": 1,
    "not_provided|Congenital_dyserythropoietic_anemia_type_4|KLF1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia_type_4|KLF1-related_disorder": 1,
    "not_provided|not_specified|Congenital_dyserythropoietic_anemia_type_4": 1,
    "Inborn_genetic_diseases|BLOOD_GROUP--LUTHERAN_INHIBITOR|FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6|Congenital_dyserythropoietic_anemia_type_4|not_provided": 1,
    "not_provided|KLF1-related_disorder": 1,
    "Glutaric_aciduria|_type_1": 696,
    "Elevated_circulating_glutaric_acid_concentration": 1,
    "Glutaric_aciduria|_type_1|not_specified": 16,
    "not_provided|Glutaric_aciduria|_type_1": 42,
    "not_provided|GCDH-related_disorder|Glutaric_aciduria|_type_1": 2,
    "Glutaric_aciduria|_type_1|not_provided": 28,
    "Glutaric_aciduria|_type_1|GCDH-related_disorder": 5,
    "Inborn_genetic_diseases|Glutaric_aciduria|_type_1": 15,
    "BLOOD_GROUP--LUTHERAN_INHIBITOR|Congenital_dyserythropoietic_anemia_type_4|FETAL_HEMOGLOBIN_QUANTITATIVE_TRAIT_LOCUS_6|Glutaric_aciduria|_type_1": 1,
    "Glutaric_aciduria|_type_1|Inborn_genetic_diseases": 10,
    "Glutaric_aciduria|_type_1|not_provided|not_specified": 2,
    "GCDH-related_disorder": 2,
    "not_specified|Glutaric_aciduria|_type_1": 14,
    "not_provided|not_specified|Glutaric_aciduria|_type_1": 2,
    "Glutaric_aciduria|_type_1|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Glutaric_aciduria|_type_1": 5,
    "GCDH-related_disorder|Glutaric_aciduria|_type_1|Abnormality_of_metabolism/homeostasis|not_provided": 1,
    "Glutaric_aciduria|_type_1|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Glutaric_aciduria|_type_1|not_provided": 1,
    "GCDH-related_disorder|Glutaric_aciduria|_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Glutaric_aciduria|_type_1|not_provided|GCDH-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Glutaric_aciduria|_type_1": 5,
    "Tyrosinemia_type_III|Glutaric_aciduria|_type_1": 1,
    "Intellectual_disability|Glutaric_aciduria|_type_1": 1,
    "Inborn_genetic_diseases|not_provided|Glutaric_aciduria|_type_1|not_specified": 1,
    "Glutaric_aciduria|_type_1|not_provided|GCDH-related_disorder": 2,
    "not_provided|Glutaric_aciduria|_type_1|not_specified": 1,
    "Inborn_genetic_diseases|GCDH-related_disorder|Glutaric_aciduria|_type_1|not_specified": 1,
    "not_provided|Glutaric_aciduria|_type_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_specified|Glutaric_aciduria|_type_1": 1,
    "Glutaric_aciduria|_type_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Glutaric_aciduria|_type_1|not_specified": 1,
    "Inborn_genetic_diseases|Glutaric_aciduria|_type_1|not_provided|Intellectual_disability": 1,
    "Glutaric_aciduria|_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Glutaric_aciduria|_type_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Glutaric_aciduria|_type_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|GCDH-related_disorder|Glutaric_aciduria|_type_1": 1,
    "not_specified|Glutaric_aciduria|_type_1|GCDH-related_disorder": 1,
    "not_provided|Hypomyelinating_leukodystrophy_2|Glutaric_aciduria|_type_1": 1,
    "Glutaric_aciduria|_type_1|Elevated_circulating_glutaric_acid_concentration|not_specified|not_provided": 1,
    "GCDH-related_disorder|not_provided|Glutaric_aciduria|_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia_29|not_provided|Glutaric_aciduria|_type_1|Abnormality_of_metabolism/homeostasis": 1,
    "Glutaric_aciduria|_type_1|not_specified|GCDH-related_disorder": 1,
    "GCDH-related_disorder|not_provided|Glutaric_aciduria|_type_1": 2,
    "GCDH-related_disorder|Glutaric_aciduria|_type_1": 1,
    "GCDH-related_disorder|Glutaric_aciduria|_type_1|Inborn_genetic_diseases|not_provided": 1,
    "GCDH-related_disorder|Inborn_genetic_diseases|Glutaric_aciduria|_type_1": 1,
    "not_specified|Elevated_circulating_glutaric_acid_concentration|Glutaric_aciduria|_type_1|not_provided": 1,
    "Elevated_circulating_glutaric_acid_concentration|not_provided|Glutaric_aciduria|_type_1|not_specified": 1,
    "FARSA-related_disorder": 7,
    "Rajab_interstitial_lung_disease_with_brain_calcifications_2": 7,
    "FARSA-related_disorder|not_provided": 3,
    "not_specified|not_provided|FARSA-related_disorder": 1,
    "not_provided|Rajab_interstitial_lung_disease_with_brain_calcifications_2": 1,
    "not_specified|FARSA-related_disorder": 1,
    "CALR-related_disorder": 5,
    "not_provided|CALR-related_disorder": 2,
    "Thrombocythemia_1|Primary_myelofibrosis|not_provided": 1,
    "not_provided|Thrombocythemia_1|Primary_myelofibrosis": 1,
    "Heterotaxy|Heterotaxy|_visceral|_13|_autosomal": 1,
    "Marshall-Smith_syndrome|Malan_overgrowth_syndrome|not_provided": 4,
    "Marshall-Smith_syndrome|not_provided": 1,
    "Marshall-Smith_syndrome|Malan_overgrowth_syndrome": 112,
    "Malan_overgrowth_syndrome|Marshall-Smith_syndrome": 61,
    "NFIX-related_disorder": 5,
    "Marshall-Smith_syndrome|Malan_overgrowth_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Malan_overgrowth_syndrome": 38,
    "not_provided|Malan_overgrowth_syndrome|Marshall-Smith_syndrome": 2,
    "Marshall-Smith_syndrome": 31,
    "not_provided|Marshall-Smith_syndrome|Malan_overgrowth_syndrome": 4,
    "Malan_overgrowth_syndrome|not_provided": 3,
    "Malan_overgrowth_syndrome|Marshall-Smith_syndrome|NFIX-related_disorder": 1,
    "not_specified|Marshall-Smith_syndrome|Malan_overgrowth_syndrome": 2,
    "Inborn_genetic_diseases|Marshall-Smith_syndrome|Malan_overgrowth_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Marshall-Smith_syndrome": 1,
    "NFIX-related_disorder|Marshall-Smith_syndrome|Malan_overgrowth_syndrome|not_provided": 1,
    "Malan_overgrowth_syndrome|Marshall-Smith_syndrome|not_specified": 2,
    "not_provided|Malan_overgrowth_syndrome": 2,
    "Malan_overgrowth_syndrome|Inborn_genetic_diseases|Marshall-Smith_syndrome": 1,
    "Malan_overgrowth_syndrome|Marfanoid_habitus_and_intellectual_disability|Marshall-Smith_syndrome": 1,
    "not_provided|NFIX-related_disorder|Malan_overgrowth_syndrome": 1,
    "NFIX-related_disorder|Malan_overgrowth_syndrome|Marshall-Smith_syndrome|Inborn_genetic_diseases": 1,
    "Marshall-Smith_syndrome|Malan_overgrowth_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Malan_overgrowth_syndrome|Marshall-Smith_syndrome|not_provided": 1,
    "Midface_retrusion|High|_narrow_palate|Strabismus|Pointed_chin|Hypoplasia_of_the_corpus_callosum|Blue_sclerae|Proptosis|Proximal_placement_of_thumb|Short_nose|Megalocornea|Global_developmental_delay|Distal_ulnar_hypoplasia|Long_fingers|Long_toe|Congenital_laryngomalacia": 1,
    "Malan_overgrowth_syndrome|Intellectual_disability": 1,
    "Malan_overgrowth_syndrome|Marshall-Smith_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Malan_overgrowth_syndrome|Marshall-Smith_syndrome": 1,
    "Malan_overgrowth_syndrome|Marshall-Smith_syndrome|not_provided": 1,
    "NFIX-related_disorder|Malan_overgrowth_syndrome|Marshall-Smith_syndrome": 1,
    "not_specified|Marshall-Smith_syndrome|Malan_overgrowth_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Marshall-Smith_syndrome": 2,
    "Marshall-Smith_syndrome|Malan_overgrowth_syndrome|Inborn_genetic_diseases|NFIX-related_disorder": 1,
    "NFIX-related_disorder|Marshall-Smith_syndrome|not_provided": 1,
    "Malan_overgrowth_syndrome|Marshall-Smith_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Marshall-Smith_syndrome|Malan_overgrowth_syndrome": 1,
    "Marshall-Smith_syndrome|Malan_overgrowth_syndrome|NFIX-related_disorder": 1,
    "Inborn_genetic_diseases|Marshall-Smith_syndrome|Malan_overgrowth_syndrome": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_68": 20,
    "TRMT1-related_disorder": 3,
    "not_provided|TRMT1-related_disorder": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_recessive_68": 3,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_recessive_68": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_68|not_provided": 3,
    "Intellectual_developmental_disorder|_autosomal_recessive_68|Inborn_genetic_diseases": 2,
    "TRMT1-related_disorder|not_provided": 1,
    "not_provided|NACC1-related_disorder": 11,
    "NACC1-related_disorder|not_provided": 11,
    "not_provided|Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination": 5,
    "NACC1-related_disorder": 7,
    "not_provided|Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination": 7,
    "Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination|NACC1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination|not_provided": 1,
    "Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination|not_provided": 2,
    "Neurodevelopmental_disorder_with_epilepsy|_cataracts|_feeding_difficulties|_and_delayed_brain_myelination|NACC1-related_disorder": 1,
    "NACC1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_42": 80,
    "CACNA1A-related_disorder": 45,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42": 4,
    "Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|not_provided": 4,
    "not_provided|Episodic_ataxia_type_2": 6,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|not_specified": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder|not_provided": 1,
    "CACNA1A-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CACNA1A-related_disorder": 6,
    "CACNA1A-related_disorder|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_provided": 2,
    "Inborn_genetic_diseases|CACNA1A-related_disorder": 1,
    "Migraine|_familial_hemiplegic|_1": 19,
    "Spinocerebellar_ataxia_type_6": 18,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6": 2,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_specified|not_provided": 1,
    "not_provided|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|not_specified": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_6": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|not_specified|not_provided|Migraine|_familial_hemiplegic|_1": 1,
    "CACNA1A-related_disorder|not_provided": 6,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|not_provided": 1,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|not_specified|not_provided": 1,
    "CACNA1A-related_disorder|not_provided|Inborn_genetic_diseases|See_cases|not_specified": 1,
    "Episodic_ataxia_type_2": 65,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 855,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided|CACNA1A-related_disorder": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 93,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 753,
    "CACNA1A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 4,
    "Inborn_genetic_diseases|not_provided|not_specified|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 7,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 26,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|Spinocerebellar_ataxia_type_6|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 1,
    "not_provided|CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 137,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided": 99,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 150,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|Inborn_genetic_diseases": 8,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 19,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Inborn_genetic_diseases": 13,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 32,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|CACNA1A-related_disorder": 7,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified": 30,
    "not_provided|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 4,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 27,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 5,
    "not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 8,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Hereditary_episodic_ataxia": 1,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|not_provided": 9,
    "Inborn_genetic_diseases|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 6,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 13,
    "not_provided|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 3,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|CACNA1A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_provided": 22,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 2,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 3,
    "not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "not_specified|CACNA1A-related_disorder": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|CACNA1A-related_disorder|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Tip-toe_gait": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_provided|Migraine|_familial_hemiplegic|_1": 1,
    "not_provided|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|not_specified": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided": 2,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided": 11,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|Migraine|_familial_hemiplegic|_1": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|not_provided": 10,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 3,
    "not_specified|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 6,
    "Developmental_and_epileptic_encephalopathy|_42|not_provided|Episodic_ataxia_type_2|Inborn_genetic_diseases|Undetermined_early-onset_epileptic_encephalopathy": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|not_specified": 1,
    "not_provided|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6": 1,
    "Migraine|_familial_hemiplegic|_1|not_provided|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 4,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|CACNA1A-related_disorder|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided": 6,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified": 2,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 3,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|not_specified|CACNA1A-related_disorder|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|EEG_with_focal_epileptiform_discharges": 1,
    "Inborn_genetic_diseases|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 11,
    "Inborn_genetic_diseases|not_provided|CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "not_specified|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Cerebellar_ataxia|not_specified|not_provided|Spinocerebellar_ataxia_type_6|Tip-toe_gait": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|CACNA1A-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2": 2,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|not_specified|not_provided": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 28,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 4,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Spinocerebellar_ataxia_type_6": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|CACNA1A-related_disorder": 1,
    "See_cases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Migraine|_familial_hemiplegic|_1|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2": 1,
    "not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 19,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|Inborn_genetic_diseases|CACNA1A-related_disorder": 1,
    "Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|CACNA1A-related_disorder": 1,
    "not_provided|Tip-toe_gait|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|See_cases": 1,
    "CACNA1A-related_disorder|not_provided|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|not_specified|not_provided": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 3,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified|Inborn_genetic_diseases|CACNA1A-related_disorder": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_provided": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided": 7,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_provided": 1,
    "Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|not_provided|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6": 1,
    "Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Intellectual_disability|Inborn_genetic_diseases|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided|not_specified": 3,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 10,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified": 5,
    "Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|Episodic_ataxia_type_2|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|CACNA1A-related_disorder|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified": 1,
    "not_provided|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|not_specified": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|not_provided|not_specified|CACNA1A-related_disorder": 1,
    "Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder": 2,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Cerebellar_ataxia": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 2,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia|_type_2|_and_epilepsy": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Migraine|_familial_hemiplegic|_1|Familial_hemiplegic_migraine": 1,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_52|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42": 3,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Generalized_hypotonia|Global_developmental_delay|Strabismus": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6": 8,
    "Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_52|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6": 1,
    "Inborn_genetic_diseases|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_52|Spinocerebellar_ataxia_type_6|not_provided": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_specified": 2,
    "Hereditary_episodic_ataxia|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_provided": 1,
    "CACNA1A-related_disorder|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided": 1,
    "CACNA1A-related_disorder|not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|CACNA1A-related_disorder": 1,
    "not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Inborn_genetic_diseases": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Neurodevelopmental_delay|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_6": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified|not_provided": 3,
    "Intellectual_disability|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Cerebellar_ataxia|Intellectual_disability|Cerebellar_atrophy|CACNA1A-related_disorder": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "Spastic_ataxia|not_provided": 1,
    "Migraine|_familial_hemiplegic|_1|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Non-progressive_congenital_cerebellar_ataxia|Ataxia___Neurologic_(child_onset)|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|Chronic_and_progressive_ataxia|not_provided|Spinocerebellar_ataxia_type_6|Neurodevelopmental_delay|Enlarged_cisterna_magna|Global_developmental_delay": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_6|not_provided": 1,
    "Episodic_ataxia_type_2|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|Migraine|_familial_hemiplegic|_1|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "not_provided|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|not_specified": 1,
    "Spinocerebellar_ataxia_type_6|not_provided|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42": 2,
    "not_specified|CACNA1A-related_disorder|Inborn_genetic_diseases|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1": 1,
    "Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "CACNA1A-related_disorder|not_specified|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_specified|CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Seizure|not_provided": 1,
    "Migraine|_familial_hemiplegic|_1|Familial_hemiplegic_migraine": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Seizure": 1,
    "CACNA1A-related_disorder|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 2,
    "CACNA1A-related_disorder|not_provided|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "Spinocerebellar_ataxia_type_6|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 3,
    "not_provided|Neurodevelopmental_delay|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "not_provided|Seizure|CACNA1A-related_disorder": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|not_specified": 1,
    "Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_52|Inborn_genetic_diseases|not_provided|Migraine": 1,
    "Developmental_and_epileptic_encephalopathy|_42|not_provided|Migraine|_familial_hemiplegic|_1": 2,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|CACNA1A-related_disorder|not_specified": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1": 1,
    "Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "CACNA1A-associated_disorders|Developmental_and_epileptic_encephalopathy|_42|Delayed_gross_motor_development|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_provided|Developmental_and_epileptic_encephalopathy|_52": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_52|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|Developmental_and_epileptic_encephalopathy|_52|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|Inborn_genetic_diseases|CACNA1A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_provided": 2,
    "not_provided|See_cases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|CACNA1A-associated_disorder": 1,
    "Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Spinocerebellar_ataxia_type_6|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_specified": 2,
    "not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1": 1,
    "Episodic_ataxia_type_2|not_provided": 1,
    "not_provided|CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_complex_neurodevelopmental_disorder|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Episodic_ataxia_type_2|not_provided|Developmental_and_epileptic_encephalopathy|_42": 1,
    "CACNA1A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_42|not_provided|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6": 1,
    "not_specified|CACNA1A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|not_provided|Episodic_ataxia_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|not_provided": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_specified|not_provided": 6,
    "not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 5,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_specified|not_provided": 1,
    "not_provided|CACNA1A-related_disorder|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "CACNA1A-related_disorder|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|not_specified": 2,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|CACNA1A-related_disorder|not_provided": 2,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|not_provided|Episodic_ataxia_type_2|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 3,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Inborn_genetic_diseases": 1,
    "not_provided|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "Inborn_genetic_diseases|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 2,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6": 1,
    "Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_provided": 3,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Epileptic_encephalopathy": 1,
    "not_provided|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|not_provided": 3,
    "Autism_spectrum_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_type_6": 3,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified": 1,
    "Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|not_provided|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_specified|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_2": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|CACNA1A-related_disorder": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2": 1,
    "CACNA1A-related_disorder|Intellectual_disability": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1": 2,
    "CACNA1A-related_disorder|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified": 1,
    "not_specified|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided|Migraine|_familial_hemiplegic|_1|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified|not_provided": 1,
    "not_provided|Hereditary_cerebellar_ataxia": 1,
    "Subependymal_giant-cell_astrocytoma|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|CACNA1A-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|CACNA1A-related_disorder": 1,
    "Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Cerebellar_ataxia|Amyotrophic_lateral_sclerosis|Chorea": 1,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|not_provided|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|not_specified": 1,
    "not_provided|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|not_specified|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Familial_hemiplegic_migraine|Migraine|_familial_hemiplegic|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|not_provided|Familial_hemiplegic_migraine|Abnormality_of_the_nervous_system": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52": 1,
    "not_provided|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|CACNA1A-related_complex_neurodevelopmental_disorder|Lennox-Gastaut_syndrome|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_specified|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1": 1,
    "not_provided|Episodic_ataxia_type_2|Inborn_genetic_diseases|Bulbar_palsy|Recurrent_respiratory_infections|Epileptic_encephalopathy|CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Familial_hemiplegic_migraine|not_provided|Migraine|_sporadic_hemiplegic|_with_progressive_cerebellar_ataxia": 1,
    "CACNA1A-related_disorder|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|not_provided|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|not_specified|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6": 1,
    "Febrile_seizure|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52": 1,
    "Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_specified|not_provided|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Familial_hemiplegic_migraine|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|not_provided|Sporadic_hemiplegic_migraine": 1,
    "CACNA1A-related_disorder|Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 2,
    "Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_6": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_52|Migraine|_familial_hemiplegic|_1": 1,
    "CACNA1A-related_complex_neurodevelopmental_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "not_provided|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CACNA1A-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|not_provided|Developmental_and_epileptic_encephalopathy|_42": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Hereditary_episodic_ataxia|not_provided": 1,
    "Global_developmental_delay|Episodic_ataxia_type_2": 1,
    "not_provided|CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified|Tip-toe_gait": 1,
    "CACNA1A-related_disorder|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Vascular_dementia": 1,
    "Global_developmental_delay|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "CACNA1A-related_disorder|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided": 1,
    "Idiopathic_hemiconvulsion-hemiplegia_syndrome|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_42|not_specified|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|not_provided|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Migraine|_familial_hemiplegic|_1": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|not_provided|not_specified": 1,
    "Tip-toe_gait|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|not_specified|not_provided|CACNA1A-related_disorder": 1,
    "not_provided|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_specified|CACNA1A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_42|Migraine|_familial_hemiplegic|_1|Spinocerebellar_ataxia_type_6|Episodic_ataxia_type_2|CACNA1A-related_complex_neurodevelopmental_disorder|Epileptic_encephalopathy|Gait_ataxia|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_52|not_provided": 1,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Hereditary_episodic_ataxia": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Inborn_genetic_diseases|CACNA1A-related_disorder|not_specified": 1,
    "Global_developmental_delay|Spinocerebellar_ataxia_type_6": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|Migraine|_familial_hemiplegic|_1": 1,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Familial_hemiplegic_migraine|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Spinocerebellar_ataxia_type_6|Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified": 1,
    "not_provided|CACNA1A-related_complex_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Familial_hemiplegic_migraine|not_provided": 1,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided|Cerebellar_ataxia|Spastic_paraparesis|Mild_global_developmental_delay|Intention_tremor|Dysarthria": 1,
    "Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Dominant|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|Inborn_genetic_diseases|not_provided": 1,
    "Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42|not_provided|not_specified": 1,
    "CACNA1A-related_disorder|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|not_provided": 2,
    "CACNA1A-related_complex_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Episodic_ataxia_type_2|Developmental_and_epileptic_encephalopathy|_42": 1,
    "CACNA1A-related_complex_neurodevelopmental_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_42|not_provided|Focal_epilepsy|Episodic_ataxia_type_2": 1,
    "Migraine|_familial_hemiplegic|_1|Developmental_and_epileptic_encephalopathy|_42|Episodic_ataxia_type_2|Spinocerebellar_ataxia_type_6": 1,
    "Severe_cystic_degeneration_of_the_brain|Infantile_epilepsy|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_recessive_3|not_provided": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_3": 4,
    "CC2D1A-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_3|not_provided": 2,
    "not_provided|CC2D1A-related_disorder": 6,
    "Intellectual_disability|_autosomal_recessive_3": 23,
    "CC2D1A-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|CC2D1A-related_disorder": 2,
    "Global_developmental_delay|Visual_impairment|Cerebral_palsy": 1,
    "CC2D1A-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_3": 6,
    "Intellectual_disability|_autosomal_recessive_3|Inborn_genetic_diseases|not_provided": 2,
    "Intellectual_disability|_autosomal_recessive_3|not_specified": 1,
    "CC2D1A-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_3": 2,
    "not_provided|not_specified|CC2D1A-related_disorder": 2,
    "Autism|not_provided|Premature_ovarian_failure_19|Intellectual_disability|_autosomal_recessive_3|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|CC2D1A-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|CC2D1A-related_disorder|Intellectual_disability|_autosomal_recessive_3": 1,
    "CC2D1A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_autosomal_recessive_3": 1,
    "not_provided|Inborn_genetic_diseases|CC2D1A-related_disorder|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_3|not_provided": 3,
    "Intellectual_disability|_autosomal_recessive_3|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_3": 2,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_3|not_specified": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_3|Inborn_genetic_diseases|CC2D1A-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_3|CC2D1A-related_disorder|Intellectual_disability|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|Intellectual_disability|_autosomal_recessive_3": 1,
    "CC2D1A-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|CC2D1A-related_disorder|Intellectual_disability|_autosomal_recessive_3": 1,
    "CC2D1A-related_disorder|Smith-Magenis_Syndrome-like|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_3": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|CC2D1A-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_3|not_provided|CC2D1A-related_disorder|Intellectual_disability|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|CC2D1A-related_disorder|Inborn_genetic_diseases": 1,
    "CC2D1A-related_disorder|not_specified|not_provided|Intellectual_disability|_autosomal_recessive_3": 1,
    "not_specified|CC2D1A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_autosomal_recessive_3|not_provided|not_specified|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|CC2D1A-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Smith-Magenis_Syndrome-like|Intellectual_disability|_autosomal_recessive_3": 1,
    "not_provided|Intellectual_disability|_autosomal_recessive_3|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_recessive_3|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_3": 1,
    "Cardioacrofacial_dysplasia_1|not_specified": 1,
    "Cardioacrofacial_dysplasia_1": 6,
    "PRKACA-related_disorder": 8,
    "PRKACA-related_disorder|not_provided": 2,
    "ACTH-independent_adrenal_Cushing_syndrome|_somatic|Pigmented_nodular_adrenocortical_disease|_primary|_4|not_provided": 1,
    "Pigmented_nodular_adrenocortical_disease|_primary|_4": 1,
    "not_provided|Cardioacrofacial_dysplasia_1": 1,
    "Cardioacrofacial_dysplasia_1|Pigmented_nodular_adrenocortical_disease|_primary|_4": 1,
    "PRKACA-related_disorder|not_specified": 1,
    "Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders": 26,
    "Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders|Inborn_genetic_diseases": 2,
    "Global_developmental_delay|Specific_learning_disability|Intellectual_disability": 1,
    "Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders|Attention_deficit_hyperactivity_disorder|Global_developmental_delay|Autistic_behavior|Seizure": 1,
    "Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders|Global_developmental_delay": 1,
    "ADGRL1-related_condition|Neurodevelopmental_disorder": 1,
    "Global_developmental_delay|Specific_learning_disability": 1,
    "Inborn_genetic_diseases|Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders": 5,
    "Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders|Attention_deficit_hyperactivity_disorder|Global_developmental_delay|Autistic_behavior|Intellectual_disability": 2,
    "Inborn_genetic_diseases|ADGRL1-related_condition": 1,
    "ADGRL1-related_condition": 1,
    "Attention_deficit_hyperactivity_disorder|Global_developmental_delay|Autistic_behavior|Seizure": 1,
    "Autistic_behavior|Attention_deficit_hyperactivity_disorder|Developmental_delay|_behavioral_abnormalities|_and_neuropsychiatric_disorders": 1,
    "Oculopharyngodistal_myopathy_2": 1,
    "GIPC1-related_condition": 1,
    "not_specified|GIPC1-related_condition": 1,
    "not_specified|not_provided|Intellectual_disability|_autosomal_recessive_14": 1,
    "TECR-related_disorder": 3,
    "Intellectual_disability|_autosomal_recessive_14": 2,
    "Intellectual_disability|_autosomal_recessive_14|not_specified|not_provided": 1,
    "not_specified|TECR-related_disorder|not_provided": 1,
    "TECR-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|TECR-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_39": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_39|Mitochondrial_disorder_due_to_a_defect_in_assembly_or_maturation_of_the_respiratory_chain_complexes": 1,
    "ADGRE2-related_disorder|not_provided": 6,
    "Autosomal_dominant_vibratory_urticaria": 2,
    "not_provided|ADGRE2-related_disorder": 9,
    "not_provided|Autosomal_dominant_vibratory_urticaria": 3,
    "ADGRE2-related_disorder|not_provided|not_specified": 1,
    "ADGRE2-related_disorder|Vibratory_urticaria|not_provided": 1,
    "not_provided|Vibratory_urticaria": 1,
    "not_specified|Autosomal_dominant_vibratory_urticaria|not_provided": 1,
    "Vibratory_urticaria|Autosomal_dominant_vibratory_urticaria|not_provided": 1,
    "Vibratory_urticaria": 6,
    "not_provided|Vibratory_urticaria|not_specified": 1,
    "Vibratory_urticaria|not_provided": 1,
    "Autosomal_dominant_vibratory_urticaria|not_specified|not_provided": 1,
    "ADGRE2-related_disorder": 10,
    "not_specified|ADGRE2-related_disorder": 1,
    "not_provided|ADGRE2-related_disorder|not_specified": 1,
    "not_specified|Vibratory_urticaria|not_provided": 1,
    "CASP14-related_disorder": 4,
    "Ichthyosis|_congenital|_autosomal_recessive_12": 2,
    "not_specified|not_provided|Ichthyosis|_congenital|_autosomal_recessive_12": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 120,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 73,
    "Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2": 1,
    "not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified": 2,
    "NOTCH3-related_disorder|not_specified": 3,
    "not_specified|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 11,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|NOTCH3-related_disorder|not_provided|not_specified": 1,
    "Lateral_meningocele_syndrome": 11,
    "not_provided|not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 9,
    "not_provided|Lateral_meningocele_syndrome": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided": 7,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|not_specified|not_provided": 2,
    "Lateral_meningocele_syndrome|not_provided": 1,
    "NOTCH3-related_disorder|not_provided": 14,
    "Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|Lateral_meningocele_syndrome": 4,
    "NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided|Inborn_genetic_diseases": 1,
    "NOTCH3-related_disorder": 20,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Inborn_genetic_diseases": 2,
    "not_provided|NOTCH3-related_disorder": 18,
    "NOTCH3-related_disorder|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 7,
    "not_provided|NOTCH3-related_disorder|not_specified": 3,
    "Inborn_genetic_diseases|NOTCH3-related_disorder": 3,
    "not_provided|NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 3,
    "Inborn_genetic_diseases|not_provided|NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|not_provided|not_specified": 1,
    "not_specified|not_provided|Pulmonary_arterial_hypertension|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "Inborn_genetic_diseases|not_provided|Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2": 1,
    "not_specified|NOTCH3-related_disorder|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 2,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified": 6,
    "Inborn_genetic_diseases|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified|not_provided": 1,
    "NOTCH3-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 7,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|Lateral_meningocele_syndrome": 2,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome": 8,
    "Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified|not_provided": 3,
    "not_provided|Lateral_meningocele_syndrome|not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 2,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified|not_provided": 3,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 25,
    "Inborn_genetic_diseases|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 3,
    "Lateral_meningocele_syndrome|not_specified|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 2,
    "Myofibromatosis|_infantile|_2": 1,
    "not_specified|not_provided|NOTCH3-related_disorder": 1,
    "not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "NOTCH3-related_disorder|Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Pulmonary_arterial_hypertension": 1,
    "NOTCH3-related_disorder|not_provided|not_specified": 3,
    "not_provided|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "not_provided|NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "Myofibromatosis|_infantile|_2|Myofibromatosis|_infantile|_1": 1,
    "NOTCH3-related_disorder|not_specified|not_provided": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 4,
    "Myofibromatosis|_infantile|_2|not_provided": 1,
    "NOTCH3-related_disorder|not_provided|Pulmonary_arterial_hypertension|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|NOTCH3-related_disorder": 3,
    "not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|Pulmonary_arterial_hypertension": 1,
    "NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided": 2,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Sneddon_syndrome|not_provided|NOTCH3-related_disorder": 1,
    "Cerebral_arterial_disease|not_provided": 1,
    "Cerebral_cavernous_malformation|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "not_provided|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|not_specified": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|NOTCH3-related_disorder": 3,
    "not_specified|not_provided|Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "not_specified|NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 2,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_specified": 2,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Inborn_genetic_diseases": 1,
    "NOTCH3-related_disorder|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 1,
    "not_provided|Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2": 3,
    "Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_specified": 1,
    "Inborn_genetic_diseases|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_specified|not_provided": 1,
    "CEREBRAL_ARTERIOPATHY|_AUTOSOMAL_RECESSIVE|_WITH_SUBCORTICAL_INFARCTS_AND_LEUKOENCEPHALOPATHY_1": 1,
    "not_specified|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 2,
    "Vascular_dementia|Inborn_genetic_diseases|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 1,
    "Auditory_neuropathy|NOTCH3-related_disorder": 1,
    "Progressive_psychomotor_deterioration": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|NOTCH3-related_disorder": 2,
    "Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|not_provided": 1,
    "not_specified|Pulmonary_arterial_hypertension|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|NOTCH3-related_disorder|Lateral_meningocele_syndrome": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy_2|not_provided": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified|not_provided|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "not_provided|NOTCH3-related_disorder|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|See_cases": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|not_specified|NOTCH3-related_disorder": 1,
    "NOTCH3-related_disorder|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|NOTCH3-related_disorder|not_specified|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 1,
    "NOTCH3-related_disorder|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|See_cases": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|not_provided|Myofibromatosis|_infantile|_2": 1,
    "NOTCH3-related_disorder|not_provided|Inborn_genetic_diseases|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "Vascular_parkinsonism|Cerebral_small_vessel_disease|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified|not_provided": 1,
    "Migraine|Tension-type_headache|Transient_ischemic_attack|Abnormal_brain_morphology": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Sneddon_syndrome|Myofibromatosis|_infantile|_2|Lateral_meningocele_syndrome|not_provided": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_specified|Lateral_meningocele_syndrome": 1,
    "Abnormal_cerebral_white_matter_morphology|Migraine_with_aura": 1,
    "not_provided|Stroke_disorder|Migraine_with_aura|Depression": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|not_provided|not_specified": 2,
    "not_specified|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|NOTCH3-related_disorder": 2,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|NOTCH3-related_disorder": 1,
    "not_specified|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|NOTCH3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 1,
    "Migraine|Depression|Migraine_with_aura|Abnormal_cerebral_white_matter_morphology|Atypical_behavior|Cognitive_impairment|Ischemic_stroke": 1,
    "Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|not_provided|NOTCH3-related_disorder|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|Lateral_meningocele_syndrome": 1,
    "not_specified|Lateral_meningocele_syndrome|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 2,
    "not_provided|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 2,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 4,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|NOTCH3-related_disorder|not_specified|not_provided": 1,
    "NOTCH3-related_disorder|Adult_onset_neurodegenerative_disorder|Migraine_without_aura|Stroke_disorder|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|not_provided": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|not_provided|NOTCH3-related_disorder": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Inborn_genetic_diseases|not_specified": 1,
    "Ischemic_stroke|Transient_ischemic_attack|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided": 1,
    "NOTCH3-related_disorder|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2": 1,
    "NOTCH3-related_disorder|Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|not_provided|Recurrent_subcortical_infarcts": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|NOTCH3-related_disorder|not_provided": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided|not_specified": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|Lateral_meningocele_syndrome|not_provided": 1,
    "not_provided|Stroke_disorder": 1,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|not_provided|NOTCH3-related_disorder": 1,
    "Inborn_genetic_diseases|Myofibromatosis|_infantile|_2": 1,
    "not_provided|Adams-Oliver_syndrome_5|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 1,
    "not_specified|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|not_provided": 2,
    "Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy|not_provided|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "not_specified|not_provided|Cerebral_arteriopathy_with_subcortical_infarcts_and_leukoencephalopathy": 1,
    "not_provided|Myofibromatosis|_infantile|_2|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Lateral_meningocele_syndrome": 1,
    "Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|CEREBRAL_ARTERIOPATHY|_AUTOSOMAL_RECESSIVE|_WITH_SUBCORTICAL_INFARCTS_AND_LEUKOENCEPHALOPATHY_1": 1,
    "NOTCH3-related_disorder|Lateral_meningocele_syndrome|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1|Myofibromatosis|_infantile|_2|not_provided": 1,
    "not_provided|BRD4-related_disorder": 11,
    "BRD4-related_disorder|not_provided": 15,
    "Cornelia_de_Lange-like_syndrome": 2,
    "BRD4-related_disorder": 14,
    "De_Lange_syndrome|not_provided|not_specified": 1,
    "See_cases|Cornelia_de_Lange_syndrome_6": 1,
    "Learning_Disabilities|_Adolescent": 1,
    "Mental_disorder|Cornelia_de_Lange_syndrome_6": 1,
    "BRD4-related_disorder|not_specified|not_provided": 1,
    "Mental_disorder": 1,
    "Autosomal_recessive_congenital_ichthyosis_5": 59,
    "Autosomal_recessive_congenital_ichthyosis_5|not_specified": 2,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_5|not_specified": 1,
    "not_provided|Autosomal_recessive_congenital_ichthyosis_5": 23,
    "Inborn_genetic_diseases|Bladder_exstrophy-epispadias-cloacal_extrophy_complex|not_provided|Autosomal_recessive_congenital_ichthyosis_5": 1,
    "not_provided|Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_5|CYP4F22-related_disorder": 1,
    "Autosomal_recessive_congenital_ichthyosis_5|not_provided": 15,
    "Autosomal_recessive_congenital_ichthyosis_5|Lamellar_ichthyosis": 3,
    "not_provided|not_specified|Autosomal_recessive_congenital_ichthyosis_5": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_congenital_ichthyosis_5": 1,
    "not_provided|CYP4F22-related_disorder": 3,
    "Autosomal_recessive_congenital_ichthyosis_5|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Autosomal_recessive_congenital_ichthyosis_5": 1,
    "CYP4F22-related_disorder|not_provided|Autosomal_recessive_congenital_ichthyosis_5": 4,
    "Autosomal_recessive_congenital_ichthyosis_5|not_specified|not_provided": 1,
    "Autosomal_recessive_congenital_ichthyosis_5|Lamellar_ichthyosis|not_provided": 1,
    "Lamellar_ichthyosis|Autosomal_recessive_congenital_ichthyosis_5": 2,
    "Congenital_ichthyosiform_erythroderma|not_provided|Autosomal_recessive_congenital_ichthyosis_5": 1,
    "CYP4F22-related_disorder": 1,
    "Atopic_eczema|Ichthyosis": 2,
    "Autosomal_recessive_congenital_ichthyosis_5|not_provided|Lamellar_ichthyosis": 1,
    "CYP4F22-related_disorder|Autosomal_recessive_congenital_ichthyosis_5": 1,
    "CYP4F2-related_disorder": 22,
    "warfarin_response_-_Dosage|acenocoumarol_response_-_Dosage|not_provided|CYP4F2-related_disorder": 1,
    "CYP4F2-related_disorder|not_provided": 1,
    "Bleeding_disorder|_platelet-type|_25": 2,
    "not_provided|Bleeding_disorder|_platelet-type|_25": 1,
    "Hypertrophic_cardiomyopathy_19": 233,
    "Hypertrophic_cardiomyopathy_19|CALR3-related_disorder|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_19": 13,
    "Hypertrophic_cardiomyopathy_19|not_specified": 10,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_19|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_19|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_19": 3,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_19": 2,
    "not_specified|Hypertrophic_cardiomyopathy_19|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_19": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_19": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_19": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_19": 1,
    "Restrictive_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_19": 1,
    "Hypertrophic_cardiomyopathy_19|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_19|CALR3-related_disorder": 2,
    "not_provided|Hypertrophic_cardiomyopathy_19": 4,
    "CALR3-related_disorder|Hypertrophic_cardiomyopathy_19|not_specified": 1,
    "Hypertrophic_cardiomyopathy_19|not_provided": 3,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_19|CALR3-related_disorder": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_19": 2,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy_19": 1,
    "Arrhythmogenic_right_ventricular_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_19": 1,
    "CALR3-related_disorder|not_provided|Hypertrophic_cardiomyopathy_19|not_specified": 2,
    "CALR3-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy_19": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_19|not_provided": 1,
    "SIN3B-related_disorder": 18,
    "SIN3B-related_disorder|not_provided": 4,
    "not_provided|SIN3B-related_disorder": 2,
    "SIN3B-associated_disorder": 1,
    "SIN3B-related_neurodevelopmental_disorder": 1,
    "not_provided|CPAMD8-related_disorder": 19,
    "CPAMD8-related_disorder": 9,
    "CPAMD8-related_disorder|not_provided": 22,
    "Anterior_segment_dysgenesis_8": 15,
    "not_provided|Inborn_genetic_diseases|CPAMD8-related_disorder": 1,
    "Anterior_segment_dysgenesis_8|Anterior_segment_dysgenesis": 1,
    "Inborn_genetic_diseases|CPAMD8-related_disorder": 1,
    "Anterior_segment_dysgenesis_8|not_provided": 2,
    "not_provided|Anterior_segment_dysgenesis_8": 1,
    "Inborn_genetic_diseases|Anterior_segment_dysgenesis_8": 1,
    "Abnormal_anterior_eye_segment_morphology": 1,
    "Anterior_segment_dysgenesis_8|Inborn_genetic_diseases|not_provided": 1,
    "CPAMD8-related_disorder|Inborn_genetic_diseases": 1,
    "MYO9B-related_disorder|not_specified": 2,
    "Celiac_disease|_susceptibility_to|_4|MYO9B-related_disorder|not_provided": 1,
    "MYO9B-related_disorder": 37,
    "MYO9B-related_disorder|not_provided": 2,
    "Muscle_weakness|Sensorimotor_neuropathy": 1,
    "Celiac_disease|_susceptibility_to|_4": 2,
    "not_provided|MYO9B-related_disorder": 1,
    "not_provided|ANO8-related_disorder": 1,
    "ANO8-related_disorder": 1,
    "GTPBP3-related_disorder": 3,
    "not_provided|GTPBP3-related_disorder": 4,
    "Combined_oxidative_phosphorylation_defect_type_23": 21,
    "GTPBP3-related_disorder|not_provided": 5,
    "Combined_oxidative_phosphorylation_defect_type_23|not_provided": 10,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_defect_type_23": 1,
    "Inborn_genetic_diseases|not_provided|GTPBP3-related_disorder": 1,
    "not_provided|Combined_oxidative_phosphorylation_defect_type_23": 4,
    "Combined_oxidative_phosphorylation_defect_type_23|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|GTPBP3-related_disorder|Combined_oxidative_phosphorylation_defect_type_23": 1,
    "not_specified|not_provided|Combined_oxidative_phosphorylation_defect_type_23": 1,
    "not_specified|GTPBP3-related_disorder|not_provided": 1,
    "GTPBP3-related_disorder|Combined_oxidative_phosphorylation_defect_type_23|not_provided": 1,
    "Inborn_genetic_diseases|PIGG-related_neurodevelopmental_disorder|Combined_oxidative_phosphorylation_defect_type_23|not_provided": 1,
    "not_provided|not_specified|GTPBP3-related_disorder": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_defect_type_23|not_provided": 1,
    "PLVAP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PLVAP-related_disorder": 2,
    "PLVAP-related_disorder|not_provided": 8,
    "not_provided|Diarrhea_10|_protein-losing_enteropathy_type": 1,
    "not_provided|not_specified|PLVAP-related_disorder": 1,
    "Diarrhea_10|_protein-losing_enteropathy_type": 4,
    "Diarrhea_10|_protein-losing_enteropathy_type|not_provided": 2,
    "Diarrhea_10|_protein-losing_enteropathy_type|Inborn_genetic_diseases|not_provided": 1,
    "HUMAN_IMMUNODEFICIENCY_VIRUS_TYPE_1|_RAPID_PROGRESSION_TO_AIDS": 1,
    "NXNL1-related_disorder": 7,
    "COLGALT1-related_disorder": 6,
    "not_provided|COLGALT1-related_disorder": 12,
    "Brain_small_vessel_disease_3": 7,
    "COLGALT1-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|Brain_small_vessel_disease_3": 1,
    "Brain_small_vessel_disease_3|not_provided": 1,
    "Brain_small_vessel_disease_3|Inborn_genetic_diseases": 1,
    "UNC13A-related_disorder": 95,
    "not_provided|UNC13A-related_disorder": 7,
    "UNC13A-related_disorder|not_provided": 11,
    "UNC13A-related_disorder|not_specified|not_provided": 2,
    "UNC13A-related_disorder|Amyotrophic_lateral_sclerosis|not_provided": 2,
    "UNC13A-related_Neurodevelopmental_and_Movement_disorder": 3,
    "UNC13A-related_disorder|not_specified": 3,
    "not_specified|UNC13A-related_disorder": 7,
    "not_provided|UNC13A-associated_disorder|Developmental_regression|Cerebellar_ataxia|Delayed_speech_and_language_development|Tremor|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Neurodevelopmental_disorder": 1,
    "Cerebellar_ataxia|Microcephaly|Tremor": 1,
    "UNC13A-related_Neurodevelopmental_disorder": 1,
    "Immunodeficiency_76": 3,
    "Immunodeficiency_76|Severe_congenital_neutropenia": 4,
    "not_provided|FCHO1-related_disorder": 4,
    "Immunodeficiency_76|not_provided": 1,
    "not_specified|Immunodeficiency_76|not_provided": 1,
    "FCHO1-related_disorder": 1,
    "FCHO1-related_disorder|not_provided": 1,
    "Immunodeficiency_with_T_and_B_cell_lymphopenia|Severe_congenital_neutropenia": 1,
    "not_provided|Immunodeficiency_76": 1,
    "Cryptorchidism": 5,
    "not_specified|not_provided|Cryptorchidism": 1,
    "Inborn_genetic_diseases|Cryptorchidism": 1,
    "INSL3-related_disorder": 2,
    "not_provided|Severe_combined_immunodeficiency_disease": 3,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_provided": 24,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 1025,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified|not_provided": 4,
    "JAK3-related_disorder": 3,
    "not_specified|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_provided": 3,
    "not_specified|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 15,
    "not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 26,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified": 9,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|Inborn_genetic_diseases": 10,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency_disease|not_specified|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 6,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|JAK3-related_disorder": 5,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|JAK3-related_disorder|not_specified|not_provided": 1,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|JAK3-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 11,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "JAK3-related_disorder|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 2,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified|Severe_combined_immunodeficiency_disease|not_provided": 1,
    "Inborn_genetic_diseases|JAK3-related_disorder": 1,
    "not_provided|not_specified|Severe_combined_immunodeficiency_disease|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 1,
    "JAK3-related_disorder|not_specified|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 1,
    "not_specified|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|JAK3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 1,
    "not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|Severe_combined_immunodeficiency_disease": 1,
    "not_provided|Severe_combined_immunodeficiency_disease|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 3,
    "Severe_combined_immunodeficiency_disease|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 1,
    "not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified": 2,
    "JAK3-related_disorder|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_provided": 2,
    "not_specified|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency": 2,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|JAK3-related_disorder|not_provided": 1,
    "not_specified|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|JAK3-related_disorder": 1,
    "Severe_combined_immunodeficiency_disease|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified": 1,
    "JAK3-related_disorder|not_provided|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|not_specified": 1,
    "not_specified|T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|Inborn_genetic_diseases": 1,
    "T-B+_severe_combined_immunodeficiency_due_to_JAK3_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Thyroid_dyshormonogenesis_1": 66,
    "not_provided|Thyroid_dyshormonogenesis_1": 20,
    "Thyroid_dyshormonogenesis_1|not_provided": 12,
    "SLC5A5-related_disorder|not_provided|Thyroid_dyshormonogenesis_1": 1,
    "SLC5A5-related_disorder|not_provided": 3,
    "Thyroid_dyshormonogenesis_1|SLC5A5-related_disorder|not_specified|not_provided": 1,
    "not_provided|SLC5A5-related_disorder": 2,
    "not_provided|SLC5A5-related_disorder|Thyroid_dyshormonogenesis_1": 2,
    "Inborn_genetic_diseases|Thyroid_dyshormonogenesis_1": 3,
    "Thyroid_dyshormonogenesis_1|not_provided|not_specified": 2,
    "Thyroid_dyshormonogenesis_1|SLC5A5-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Thyroid_dyshormonogenesis_1": 2,
    "Thyroid_dyshormonogenesis_1|not_provided|SLC5A5-related_disorder": 2,
    "Thyroid_dyshormonogenesis_1|Congenital_hypothyroidism|not_provided": 1,
    "not_provided|SLC5A5-related_disorder|not_specified": 1,
    "not_specified|not_provided|Thyroid_dyshormonogenesis_1": 1,
    "not_provided|Thyroid_dyshormonogenesis_1|not_specified": 2,
    "Thyroid_Hormonogenesis_Defect": 6,
    "Thyroid_Hormonogenesis_Defect|not_provided": 2,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_specified|not_provided": 7,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 431,
    "Inborn_genetic_diseases|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 22,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|Inborn_genetic_diseases": 21,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|IL12RB1-related_disorder|not_provided": 3,
    "IL12RB1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_provided": 3,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_provided": 16,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_provided|Immunodeficiency_27A": 1,
    "IL12RB1-related_disorder": 7,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_provided|IL12RB1-related_disorder": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|IL12RB1-related_disorder": 5,
    "IL12RB1-related_disorder|not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 2,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 6,
    "not_specified|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 1,
    "IL12RB1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 4,
    "Inherited_Immunodeficiency_Diseases|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 2,
    "Mycobacterium_tuberculosis|_susceptibility_to|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency": 1,
    "Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_specified": 2,
    "not_provided|IL12RB1-related_disorder|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|Immunodeficiency_27A": 1,
    "Immunodeficiency_27A|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_specified|not_provided": 2,
    "not_provided|Mendelian_susceptibility_to_mycobacterial_diseases_due_to_complete_IL12RB1_deficiency|not_specified": 1,
    "MAST3-related_disorder": 6,
    "Developmental_and_epileptic_encephalopathy_108": 16,
    "Inborn_genetic_diseases|MAST3-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_108": 2,
    "not_provided|MAST3-related_disorder|Developmental_and_epileptic_encephalopathy_108|Pervasive_developmental_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_108|Inborn_genetic_diseases": 1,
    "PIK3R2-related_disorder": 18,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 227,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_specified": 2,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Inborn_genetic_diseases": 13,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_provided": 13,
    "Inborn_genetic_diseases|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 12,
    "PIK3R2-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 7,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Intellectual_disability": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|PIK3R2-related_disorder|not_specified": 1,
    "not_provided|not_specified|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 6,
    "Inborn_genetic_diseases|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_provided": 2,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_specified": 2,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|PIK3R2-related_disorder": 3,
    "PIK3R2-related_disorder|not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 2,
    "not_specified|not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|PIK3R2-related_disorder": 2,
    "PIK3R2-related_disorder|not_specified|not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 1,
    "not_specified|Inborn_genetic_diseases|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes|PIK3R2-related_disorder|Inborn_genetic_diseases|not_provided|Megalencephaly-capillary_malformation-polymicrogyria_syndrome|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Intellectual_disability|Seizure": 1,
    "PIK3R2-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Seizure|not_provided": 1,
    "not_specified|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|PIK3R2-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_provided|not_specified": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|PIK3R2-related_disorder|not_provided": 1,
    "PIK3R2-related_disorder|not_provided": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Overgrowth_syndrome_and/or_cerebral_malformations_due_to_abnormalities_in_MTOR_pathway_genes": 1,
    "not_provided|Seizure|PIK3R2-related_disorder": 1,
    "Overgrowth_syndrome_and/or_cerebral_malformations|not_provided": 1,
    "not_provided|PIK3R2-related_disorder|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1": 2,
    "not_provided|Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|Inborn_genetic_diseases": 1,
    "Megalencephaly-polymicrogyria-polydactyly-hydrocephalus_syndrome_1|not_provided|not_specified": 1,
    "RAB3A-related_condition": 2,
    "Spermatogenic_failure_78": 3,
    "Hyperemesis_gravidarum|_susceptibility_to": 1,
    "Cold-induced_sweating_syndrome_1": 22,
    "CRLF1-related_disorder|not_provided": 1,
    "not_provided|Cold-induced_sweating_syndrome_1": 2,
    "Crisponi/Cold-induced_sweating_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Cold-induced_sweating_syndrome_1|CRLF1-related_disorder": 1,
    "not_specified|not_provided|CRLF1-related_disorder": 1,
    "Cold-induced_sweating_syndrome_1|not_specified": 1,
    "not_provided|Cone-rod_dystrophy_12|Cold-induced_sweating_syndrome_1": 1,
    "CRLF1-related_disorder": 1,
    "not_specified|Cold-induced_sweating_syndrome_1": 1,
    "Cold-induced_sweating_syndrome|Cold-induced_sweating_syndrome_1": 1,
    "Cold-induced_sweating_syndrome": 3,
    "CRTC1-related_condition": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_Epiphyseal_Dysplasia|_Dominant": 1,
    "Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 11,
    "Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided": 5,
    "Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_specified|not_provided": 3,
    "COMP-related_disorder": 9,
    "not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|not_specified": 1,
    "Multiple_epiphyseal_dysplasia_type_1|Connective_tissue_disorder|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_1": 27,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|not_provided": 19,
    "Pseudoachondroplasia|_severe|Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided": 2,
    "Multiple_epiphyseal_dysplasia|not_provided": 2,
    "Carpal_tunnel_syndrome_2|Multiple_epiphyseal_dysplasia_type_1|Multiple_epiphyseal_dysplasia|not_provided": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|not_provided|Connective_tissue_disorder": 1,
    "Carpal_tunnel_syndrome_2": 3,
    "Multiple_epiphyseal_dysplasia_type_1|not_provided": 4,
    "COMP-related_disorder|not_provided": 4,
    "Multiple_epiphyseal_dysplasia_type_1|Inborn_genetic_diseases|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided": 1,
    "not_provided|Connective_tissue_disorder|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1": 1,
    "not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "Multiple_epiphyseal_dysplasia_type_1|Carpal_tunnel_syndrome_2|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 11,
    "Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided|not_specified|Carpal_tunnel_syndrome_2": 1,
    "not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia|COMP-related_disorder": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia|Carpal_tunnel_syndrome_2|Multiple_epiphyseal_dysplasia_type_1": 1,
    "not_provided|Multiple_epiphyseal_dysplasia_type_1": 2,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|COMP-related_disorder|not_provided": 1,
    "Multiple_epiphyseal_dysplasia_type_1|Multiple_epiphyseal_dysplasia|not_provided": 1,
    "not_provided|COMP-related_disorder": 5,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|Carpal_tunnel_syndrome_2": 1,
    "not_provided|Multiple_epiphyseal_dysplasia_type_1|Multiple_epiphyseal_dysplasia": 1,
    "not_specified|not_provided|COMP-related_disorder": 1,
    "Multiple_epiphyseal_dysplasia|not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1": 1,
    "COMP-related_disorder|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 1,
    "not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1": 4,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_specified|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_1|_severe": 2,
    "not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|Carpal_tunnel_syndrome_2": 1,
    "Connective_tissue_disorder|Multiple_epiphyseal_dysplasia_type_1|not_specified|not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 1,
    "not_provided|Multiple_epiphyseal_dysplasia_type_1|Carpal_tunnel_syndrome_2|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia": 1,
    "Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|not_provided|COMP-related_disorder": 1,
    "not_specified|not_provided|Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 1,
    "not_provided|Multiple_epiphyseal_dysplasia_type_1|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome": 1,
    "Inborn_genetic_diseases|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|not_provided": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1": 12,
    "Connective_tissue_disorder|Carpal_tunnel_syndrome_2|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|not_specified|not_provided": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|Connective_tissue_disorder|not_provided": 1,
    "Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|COMP-related_disorder|not_provided|not_specified": 1,
    "Connective_tissue_disorder|not_provided|Pseudoachondroplastic_spondyloepiphyseal_dysplasia_syndrome|Multiple_epiphyseal_dysplasia_type_1|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Hypertelorism|Frontal_bossing|High_anterior_hairline|Thin_upper_lip_vermilion": 1,
    "Global_developmental_delay|Hypertelorism|Frontal_bossing|High_anterior_hairline|Strabismus": 1,
    "Mild_global_developmental_delay|Attention_deficit_hyperactivity_disorder|Delayed_speech_and_language_development|Atypical_behavior|Autistic_behavior|Short_stature": 1,
    "UPF1-related_disorder": 1,
    "Right_atrial_isomerism|Congenital_heart_defects|_multiple_types|_6": 1,
    "Right_atrial_isomerism": 3,
    "not_provided|Congenital_heart_defects|_multiple_types|_6|Right_atrial_isomerism|Heart|_malformation_of|Congenital_heart_defects|_multiple_types": 1,
    "GDF1-related_disorder": 10,
    "Congenital_heart_defects|_multiple_types|_6|not_provided|Right_atrial_isomerism": 1,
    "Visceral_heterotaxy|Progressive_myoclonic_epilepsy_type_8": 1,
    "not_provided|GDF1-related_disorder": 2,
    "Congenital_heart_defects|_multiple_types|_6": 6,
    "not_specified|not_provided|GDF1-related_disorder": 1,
    "not_provided|not_specified|GDF1-related_disorder": 1,
    "GDF1-related_disorder|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_6|Right_atrial_isomerism|not_provided": 1,
    "not_specified|GDF1-related_disorder": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_6": 2,
    "Right_atrial_isomerism|not_provided": 1,
    "GDF1-related_disorder|Double_outlet_right_ventricle": 1,
    "GDF1-RELATED_DISORDERS|GDF1-related_disorder|Right_atrial_isomerism|Congenital_heart_defects|_multiple_types|_6|not_provided|Transposition_of_the_great_arteries": 1,
    "Heterotaxy|not_provided|Inborn_genetic_diseases|Right_atrial_isomerism": 1,
    "Right_atrial_isomerism|Congenital_heart_defects|_multiple_types|_6|not_specified|not_provided": 1,
    "not_provided|Right_atrial_isomerism|Congenital_heart_defects|_multiple_types|_6": 1,
    "Progressive_myoclonic_epilepsy_type_8": 237,
    "GDF1-related_disorder|Progressive_myoclonic_epilepsy_type_8|not_provided|Tetralogy_of_Fallot": 1,
    "Progressive_myoclonic_epilepsy_type_8|not_specified|Visceral_heterotaxy|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_8|not_specified": 12,
    "CERS1-related_disorder|Progressive_myoclonic_epilepsy_type_8": 2,
    "not_specified|Progressive_myoclonic_epilepsy_type_8": 13,
    "not_provided|not_specified|Progressive_myoclonic_epilepsy_type_8": 1,
    "Progressive_myoclonic_epilepsy_type_8|not_provided": 7,
    "not_provided|Progressive_myoclonic_epilepsy_type_8|not_specified": 2,
    "CERS1-related_disorder": 1,
    "Progressive_myoclonic_epilepsy_type_8|not_specified|not_provided": 1,
    "Progressive_myoclonic_epilepsy_type_8|CERS1-related_disorder": 2,
    "not_provided|Progressive_myoclonic_epilepsy_type_8": 2,
    "Progressive_myoclonic_epilepsy_type_8|not_provided|not_specified": 1,
    "not_specified|not_provided|Progressive_myoclonic_epilepsy_type_8": 1,
    "CERS1-related_disorder|Progressive_myoclonic_epilepsy_type_8|not_specified": 1,
    "not_specified|Progressive_myoclonic_epilepsy_type_8|not_provided": 1,
    "Keratoconus_5": 1,
    "SLC25A42-related_disorder|not_provided": 1,
    "not_provided|SLC25A42-related_disorder": 2,
    "SLC25A42-related_mitochondrial_encephalomyopathy": 1,
    "SLC25A42-related_disorder": 1,
    "SLC25A42-related_mitochondrial_disorder|Inborn_mitochondrial_myopathy|Metabolic_crises|_recurrent|_with_variable_encephalomyopathic_features_and_neurologic_regression": 1,
    "Neurodegeneration|_infantile-onset|_with_optic_atrophy_and_brain_abnormalities": 3,
    "Neurodegeneration|_infantile-onset|_with_optic_atrophy_and_brain_abnormalities|not_specified": 1,
    "MHC_class_II_deficiency_5": 1,
    "MHC_class_II_deficiency_2": 5,
    "not_provided|MHC_class_II_deficiency|MHC_class_II_deficiency_1": 1,
    "RFXANK-related_disorder": 2,
    "MHC_class_II_deficiency_2|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_2|MHC_class_II_deficiency_3|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_1|MHC_class_II_deficiency|Inborn_genetic_diseases": 1,
    "MHC_class_II_deficiency|MHC_class_II_deficiency_2": 4,
    "MHC_class_II_deficiency_2|MHC_class_II_deficiency_1|not_provided|MHC_class_II_deficiency": 1,
    "MHC_class_II_deficiency_1|not_provided|MHC_class_II_deficiency|MHC_class_II_deficiency_2": 1,
    "MHC_class_II_deficiency|MHC_class_II_deficiency_2|RFXANK-related_disorder": 1,
    "RFXANK-related_disorder|MHC_class_II_deficiency": 1,
    "Inherited_Immunodeficiency_Diseases|MHC_class_II_deficiency_2": 1,
    "MHC_class_II_deficiency|RFXANK-related_disorder": 2,
    "GATAD2A-associated_neurodevelopmental_disorder": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_28": 5,
    "Hurthle_cell_carcinoma_of_thyroid": 1,
    "Hurthle_cell_carcinoma_of_thyroid|Mitochondrial_complex_I_deficiency|_nuclear_type_28": 2,
    "not_provided|NDUFA13-related_disorder": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_28|Mitochondrial_complex_I_deficiency|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_28": 1,
    "Retinal_dystrophy|Congenital_nephrotic_syndrome|Microphthalmia|Microcephaly|Cataract": 1,
    "Mitochondrial_complex_III_deficiency|_nuclear_type_10|Propionic_acidemia|Cardiomyopathy|Lactic_acidosis": 2,
    "Mitochondrial_complex_III_deficiency|_nuclear_type_10": 1,
    "not_provided|Mitochondrial_complex_III_deficiency|_nuclear_type_10": 2,
    "Neurodegeneration_with_brain_iron_accumulation_4": 134,
    "Neurodegeneration_with_brain_iron_accumulation_4|not_provided": 4,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_4": 12,
    "Hereditary_spastic_paraplegia_43|not_provided|not_specified|Hereditary_spastic_paraplegia|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Hereditary_spastic_paraplegia_43": 90,
    "Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia_43": 7,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_43|Hereditary_spastic_paraplegia|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Hereditary_spastic_paraplegia|Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia_43|Hereditary_spastic_paraplegia_5A|not_provided|Dystonic_disorder|Adult-onset_night_blindness|Peripheral_visual_field_loss|Mental_deterioration|Tremor|not_specified": 1,
    "not_provided|Hereditary_spastic_paraplegia_43": 4,
    "Neurodegeneration_with_brain_iron_accumulation_4|Abnormal_central_motor_function|Hereditary_spastic_paraplegia_43|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B": 11,
    "Hereditary_spastic_paraplegia_43|not_provided": 4,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Hereditary_spastic_paraplegia_43|not_specified|not_provided|Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Neurodegeneration_with_brain_iron_accumulation|C19orf12-related_disorder": 1,
    "not_provided|Hereditary_spastic_paraplegia_43|not_specified": 1,
    "Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation_4|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation|not_provided|C19orf12-related_disorder": 1,
    "Hereditary_spastic_paraplegia_43|Hereditary_spastic_paraplegia": 1,
    "Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia_43|not_specified|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_4|not_provided|Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation|Dystonic_disorder|Adult-onset_night_blindness|Peripheral_visual_field_loss|Mental_deterioration|Tremor": 1,
    "Hereditary_spastic_paraplegia_43|not_provided|Hereditary_spastic_paraplegia|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia_43|not_provided|Neurodegeneration_with_brain_iron_accumulation|Neurofibromatosis|_type_1": 1,
    "not_specified|Hereditary_spastic_paraplegia_43": 1,
    "Hereditary_spastic_paraplegia_43|not_specified": 4,
    "not_provided|Global_developmental_delay|Intellectual_disability|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "not_specified|Hereditary_spastic_paraplegia_43|not_provided": 2,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation|Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Hereditary_spastic_paraplegia|Brain_iron_accummulation|Neurodegeneration|Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_4|not_provided|Hereditary_spastic_paraplegia_43": 1,
    "Hereditary_spastic_paraplegia_43|not_provided|not_specified|Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia": 1,
    "Neurodegeneration_with_brain_iron_accumulation_4|Hereditary_spastic_paraplegia_43|not_provided": 1,
    "Hereditary_spastic_paraplegia_43|C19orf12-related_disorder": 1,
    "C19orf12-related_disorder": 1,
    "Hereditary_spastic_paraplegia_43|Neurodegeneration_with_brain_iron_accumulation_4|not_provided|Neurodegeneration_with_brain_iron_accumulation|Abnormality_of_iron_homeostasis": 1,
    "not_specified|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "Neurodegeneration_with_brain_iron_accumulation_4|not_specified": 1,
    "not_specified|not_provided|Neurodegeneration_with_brain_iron_accumulation_4": 1,
    "TSHZ3-related_disorder": 23,
    "not_provided|TSHZ3-related_disorder": 6,
    "not_specified|TSHZ3-related_disorder": 1,
    "TSHZ3-related_disorder|not_provided": 1,
    "TSHZ3-related_disorder|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|TSHZ3-related_disorder": 1,
    "RGS9BP-related_disorder|not_provided": 4,
    "RGS9BP-related_disorder": 1,
    "Prolonged_electroretinal_response_suppression_2": 3,
    "Bradyopsia": 2,
    "Bradyopsia|not_provided|Retinal_dystrophy": 1,
    "not_provided|Prolonged_electroretinal_response_suppression_2|Retinal_dystrophy": 1,
    "Prolonged_electroretinal_response_suppression_2|not_provided": 1,
    "SLC7A9-related_disorder": 11,
    "SLC7A9-related_disorder|Cystinuria": 2,
    "SLC7A9-related_disorder|not_specified|not_provided": 1,
    "Cystine_urolithiasis|Cystinuria|not_provided": 1,
    "SLC7A9-related_disorder|Cystinuria|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Cystinuria": 1,
    "Cystinuria|not_provided|not_specified": 1,
    "not_provided|SLC7A9-related_disorder|Cystinuria": 1,
    "SLC7A9-related_disorder|not_provided|Cystinuria": 3,
    "SLC7A9-related_disorder|not_provided": 4,
    "not_provided|Cystinuria|SLC7A9-related_disorder": 2,
    "Cystinuria|not_specified|not_provided": 4,
    "not_provided|SLC7A9-related_disorder": 3,
    "SLC7A9-related_disorder|Inborn_genetic_diseases|not_provided|Cystinuria": 1,
    "Cystinuria|Inborn_genetic_diseases|not_provided": 1,
    "Cystinuria|SLC7A9-related_disorder|not_provided": 1,
    "Cystinuria|not_provided|Inborn_genetic_diseases": 1,
    "CEP89-related_disorder|not_provided": 2,
    "not_provided|CEP89-related_disorder": 2,
    "FAAP24-related_disorder": 3,
    "FAAP24-related_disorder|not_provided": 2,
    "not_provided|FAAP24-related_disorder": 1,
    "Acute_myeloid_leukemia|not_provided|Inborn_genetic_diseases": 8,
    "Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia": 12,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|not_specified|Acute_myeloid_leukemia|not_provided": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "CEBPA-related_disorder|Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia": 2,
    "not_provided|Inborn_genetic_diseases|Acute_myeloid_leukemia": 4,
    "Inborn_genetic_diseases|not_specified|not_provided|Acute_myeloid_leukemia": 2,
    "CEBPA-related_disorder|Acute_myeloid_leukemia|Inborn_genetic_diseases": 2,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|CEBPA-related_disorder": 3,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|not_provided": 8,
    "Acute_myeloid_leukemia|CEBPA-related_disorder|Inborn_genetic_diseases": 3,
    "not_specified|Acute_myeloid_leukemia|CEBPA-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Acute_myeloid_leukemia|Inborn_genetic_diseases": 2,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 3,
    "Acute_myeloid_leukemia|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|CEBPA-related_disorder": 1,
    "CEBPA-related_disorder": 6,
    "Autosomal_dominant_familial_acute_myeloid_leukemia|Inborn_genetic_diseases|not_specified|not_provided|Acute_myeloid_leukemia": 1,
    "CEBPA-related_disorder|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Acute_myeloid_leukemia|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|CEBPA-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 2,
    "not_provided|Acute_myeloid_leukemia|Inborn_genetic_diseases": 5,
    "Acute_myeloid_leukemia|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|CEBPA-related_disorder|not_provided|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|CEBPA-related_disorder|not_provided|Acute_myeloid_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia": 2,
    "Acute_myeloid_leukemia|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "CEBPA-related_disorder|not_provided|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|CEBPA-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Acute_myeloid_leukemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome": 2,
    "Acute_myeloid_leukemia|not_provided|CEBPA-related_disorder|Inborn_genetic_diseases": 1,
    "CEBPA-related_disorder|Inborn_genetic_diseases": 2,
    "CEBPA-related_disorder|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia|CEBPA-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Acute_myeloid_leukemia": 2,
    "Inborn_genetic_diseases|CEBPA-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|CEBPA-related_disorder|Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia|not_specified": 1,
    "Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome|CEBPA-related_disorder": 1,
    "Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia": 1,
    "CEBPA-related_disorder|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "CEBPA-related_disorder|not_provided|Acute_myeloid_leukemia": 1,
    "Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Acute_myeloid_leukemia|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Acute_myeloid_leukemia|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Acute_myeloid_leukemia": 1,
    "not_specified|Inborn_genetic_diseases|Acute_myeloid_leukemia": 2,
    "Acute_myeloid_leukemia|CEBPA-related_disorder": 1,
    "not_specified|CEBPA-related_disorder": 1,
    "Prolidase_deficiency": 29,
    "Prolidase_deficiency|not_provided": 36,
    "not_provided|Prolidase_deficiency": 29,
    "Prolidase_deficiency|not_specified|not_provided": 3,
    "PEPD-related_disorder": 1,
    "Prolidase_deficiency|PEPD-related_disorder|not_provided": 3,
    "Prolidase_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Prolidase_deficiency": 1,
    "not_provided|Prolidase_deficiency|PEPD-related_disorder": 2,
    "PEPD-related_disorder|Prolidase_deficiency|not_provided|not_specified": 1,
    "not_provided|Prolidase_deficiency|Inborn_genetic_diseases": 1,
    "Anorectal_anomaly": 1,
    "Inborn_genetic_diseases|not_provided|Prolidase_deficiency": 1,
    "Inborn_genetic_diseases|Prolidase_deficiency|not_provided": 1,
    "not_provided|PEPD-related_disorder": 6,
    "Prolidase_deficiency|not_specified|PEPD-related_disorder|not_provided": 1,
    "Prolidase_deficiency|not_provided|Megaconial_type_congenital_muscular_dystrophy": 1,
    "PEPD-related_disorder|not_provided": 3,
    "not_specified|Prolidase_deficiency|not_provided": 1,
    "CHST8-related_disorder": 4,
    "CHST8-related_disorder|not_provided|Peeling_skin_syndrome_type_A": 1,
    "not_provided|CHST8-related_disorder": 1,
    "KIAA0355-related_condition": 1,
    "Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency|GPI-related_disorder": 1,
    "GPI-related_disorder": 8,
    "Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 73,
    "Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency|Inborn_genetic_diseases": 6,
    "not_provided|GPI-related_disorder": 1,
    "not_provided|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 13,
    "Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency|not_provided": 8,
    "not_specified|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency|not_provided": 1,
    "not_provided|Hemolytic_anemia|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 1,
    "not_provided|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency|GPI-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 3,
    "GPI-related_disorder|Inborn_genetic_diseases|not_provided|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 1,
    "not_provided|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|GPI-related_disorder|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 3,
    "Inborn_genetic_diseases|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 2,
    "Inborn_genetic_diseases|GPI-related_disorder|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Hemolytic_anemia_due_to_glucophosphate_isomerase_deficiency": 1,
    "ACCES_syndrome": 14,
    "UBA2-related_disorder": 4,
    "not_provided|ACCES_syndrome": 3,
    "UBA2-related_neurodevelopmental_disorder_with_multiple_anomalies": 1,
    "Ectrodactyly|ACCES_syndrome": 1,
    "ACCES_syndrome|UBA2-related_disorder|not_provided": 1,
    "Chromosome_19q13.11_deletion_syndrome|_distal": 1,
    "Inborn_genetic_diseases|ACCES_syndrome": 2,
    "ACCES_syndrome|not_provided": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 10,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 6,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Developmental_and_epileptic_encephalopathy|_52|Brugada_syndrome_5": 4,
    "not_specified|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "not_provided|Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 2,
    "not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Brugada_syndrome_5": 1,
    "Brugada_syndrome_5|not_provided": 25,
    "Brugada_syndrome_5": 256,
    "Cardiovascular_phenotype|not_provided|Brugada_syndrome_5": 14,
    "Cardiovascular_phenotype|Brugada_syndrome_5|not_provided": 2,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_5": 5,
    "not_provided|Brugada_syndrome_5": 34,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Cardiovascular_phenotype|SCN1B-related_disorder|not_provided|Brugada_syndrome_5|not_specified": 1,
    "Brugada_syndrome_5|Cardiovascular_phenotype": 18,
    "Cardiovascular_phenotype|Brugada_syndrome_5": 16,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|not_provided|not_specified": 1,
    "not_specified|Brugada_syndrome_5": 8,
    "Brugada_syndrome_5|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_5|SCN1B-related_disorder|not_provided": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Developmental_and_epileptic_encephalopathy|_52": 2,
    "Brugada_syndrome_5|not_provided|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_5|Cardiovascular_phenotype|Childhood_absence_epilepsy|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_5": 4,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Developmental_and_epileptic_encephalopathy|_52|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52|not_provided": 1,
    "Brugada_syndrome_5|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Cardiovascular_phenotype": 1,
    "Brugada_syndrome_5|Severe_myoclonic_epilepsy_in_infancy": 1,
    "Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Brugada_syndrome_5|Cardiovascular_phenotype": 3,
    "Undetermined_early-onset_epileptic_encephalopathy|Cardiovascular_phenotype|not_provided|Brugada_syndrome_5": 1,
    "Brugada_syndrome_5|not_specified": 7,
    "not_provided|Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|SCN1B-related_disorder": 1,
    "not_specified|Brugada_syndrome_5|Cardiovascular_phenotype": 3,
    "Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Brugada_syndrome_5|Cardiovascular_phenotype": 1,
    "SCN1B-related_disorder": 2,
    "not_provided|Cardiovascular_phenotype|Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52": 1,
    "not_provided|SCN1B-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Brugada_syndrome_5": 1,
    "not_provided|Conduction_system_disorder|Developmental_and_epileptic_encephalopathy|_52": 1,
    "Cardiovascular_phenotype|Epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Cardiovascular_phenotype|not_provided": 1,
    "SCN1B-related_disorder|Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|not_specified|Brugada_syndrome_5": 3,
    "Cardiovascular_phenotype|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|not_provided": 1,
    "Brugada_syndrome_5|SCN1B-related_disorder": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_52": 4,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|Cardiovascular_phenotype": 1,
    "SCN1B-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Brugada_syndrome_5": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Cardiovascular_phenotype|Brugada_syndrome_5|not_provided|not_specified": 1,
    "Brugada_syndrome_5|Cardiovascular_phenotype|not_provided": 3,
    "Cardiovascular_phenotype|SCN1B-related_disorder|Atrial_fibrillation|_familial|_13|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|not_provided|Generalized_epilepsy_with_febrile_seizures_plus": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13|Seizure": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13|Developmental_and_epileptic_encephalopathy|_52|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_1|Atrial_fibrillation|_familial|_1": 1,
    "Cardiovascular_phenotype|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13": 1,
    "Long_QT_syndrome|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|SCN1B-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|not_provided": 1,
    "not_specified|not_provided|Brugada_syndrome_5": 5,
    "Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_1|not_provided|Brugada_syndrome_5": 1,
    "SCN1B-related_disorder|not_provided|Brugada_syndrome_5": 1,
    "Atrial_fibrillation|_familial|_13|not_provided|Brugada_syndrome_5": 1,
    "not_specified|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13": 1,
    "not_specified|SCN1B-related_disorder|Brugada_syndrome_5": 1,
    "Brugada_syndrome_5|not_provided|not_specified|Ventricular_fibrillation": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "Brugada_syndrome_5|not_specified|not_provided": 4,
    "not_provided|Brugada_syndrome_5|not_specified": 2,
    "Brugada_syndrome_5|Cardiovascular_phenotype|not_specified": 2,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|not_specified|not_provided|Long_QT_syndrome|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "Atrial_fibrillation|_familial|_13|Brugada_syndrome_5|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13": 1,
    "Cardiac_arrhythmia|not_specified|not_provided|Brugada_syndrome_5": 2,
    "SCN1B-related_disorder|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Developmental_and_epileptic_encephalopathy|_52|Brugada_syndrome_5|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_5|not_specified|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Developmental_and_epileptic_encephalopathy|_52": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52|Brugada_syndrome_5|not_specified|not_provided|Death_in_early_adulthood": 1,
    "not_provided|SCN1B-related_disorder|Cardiovascular_phenotype|Brugada_syndrome_5": 1,
    "not_provided|Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|SCN1B-related_disorder|not_specified|Brugada_syndrome_5": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Brugada_syndrome_5|See_cases|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Generalized_epilepsy_with_febrile_seizures_plus|_type_1": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 2,
    "Brugada_syndrome_5|not_provided|Cardiovascular_phenotype": 2,
    "Brugada_syndrome_5|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52|Atrial_fibrillation|_familial|_13|not_provided": 1,
    "not_provided|Brugada_syndrome_5|Cardiovascular_phenotype|Atrial_fibrillation|_familial|_13|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Developmental_and_epileptic_encephalopathy|_52": 1,
    "SCN1B-related_disorder|Cardiovascular_phenotype|Developmental_and_epileptic_encephalopathy|_52|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|Atrial_fibrillation|_familial|_13|not_provided": 1,
    "Brugada_syndrome_5|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Atrial_fibrillation|_familial|_13|Developmental_and_epileptic_encephalopathy|_52|not_specified|not_provided": 1,
    "Brugada_syndrome_5|not_specified|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|SCN1B-related_disorder|Brugada_syndrome_5|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Developmental_and_epileptic_encephalopathy|_52|not_provided|Brugada_syndrome_5": 1,
    "Cardiovascular_phenotype|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5": 4,
    "not_specified|Developmental_and_epileptic_encephalopathy|_52": 1,
    "not_provided|Generalized_epilepsy_with_febrile_seizures_plus|_type_1|Brugada_syndrome_5|not_specified": 1,
    "Arthrogryposis_multiplex_congenita_1|_neurogenic|_with_myelin_defect|not_provided": 8,
    "LGI4-related_disorder": 6,
    "Inborn_genetic_diseases|LGI4-related_disorder": 1,
    "Arthrogryposis_multiplex_congenita_1|_neurogenic|_with_myelin_defect": 21,
    "Arthrogryposis_multiplex_congenita_1|_neurogenic|_with_myelin_defect|Inborn_genetic_diseases|not_provided": 1,
    "LGI4-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|Arthrogryposis_multiplex_congenita_1|_neurogenic|_with_myelin_defect": 1,
    "not_provided|Hemochromatosis_type_2B|Hereditary_hemochromatosis": 1,
    "Hereditary_hemochromatosis|not_provided|Hemochromatosis_type_2B": 1,
    "Hemochromatosis_type_2B|Hereditary_hemochromatosis": 2,
    "Hemochromatosis_type_2B": 8,
    "not_specified|Hemochromatosis_type_2B|Hereditary_hemochromatosis": 1,
    "Hemochromatosis|_juvenile|_digenic": 1,
    "Hereditary_hemochromatosis|Hemochromatosis_type_2B": 2,
    "Inborn_genetic_diseases|HAMP-related_disorder|Hemochromatosis_type_2B": 1,
    "Hemochromatosis_type_2B|Hereditary_hemochromatosis|not_specified": 1,
    "HAMP-related_disorder|Hemochromatosis_type_1|Hereditary_hemochromatosis|not_specified|not_provided|Hemochromatosis_type_2B|Hemochromatosis|_type_2a|_modifier_of": 1,
    "Hereditary_hemochromatosis|not_specified|Hemochromatosis_type_2B": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia_75": 1,
    "MAG-related_disorder|Hereditary_spastic_paraplegia_75": 1,
    "Hereditary_spastic_paraplegia_75": 192,
    "Hereditary_spastic_paraplegia_75|not_provided": 10,
    "Hereditary_spastic_paraplegia_75|not_specified|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_75": 8,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_75": 17,
    "Hereditary_spastic_paraplegia_75|MAG-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_75|Inborn_genetic_diseases": 11,
    "Hereditary_spastic_paraplegia_75|MAG-related_disorder": 3,
    "Hereditary_spastic_paraplegia_75|MAG-related_disorder|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_75|not_specified|MAG-related_disorder": 2,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_75|not_provided": 1,
    "Hereditary_spastic_paraplegia_75|not_provided|MAG-related_disorder": 2,
    "Hereditary_spastic_paraplegia_75|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_75|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia_75": 1,
    "MAG-related_disorder": 1,
    "Hereditary_spastic_paraplegia_75|not_specified": 1,
    "MAG-related_disorder|Hereditary_spastic_paraplegia_75|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_75": 1,
    "not_provided|MAG-related_disorder|Hereditary_spastic_paraplegia_75|not_specified": 1,
    "Neurodevelopmental_disorder_with_facial_dysmorphism|_absent_language|_and_pseudo-pelger-huet_anomaly|Inborn_genetic_diseases|not_provided": 1,
    "Neurodevelopmental_disorder_with_facial_dysmorphism|_absent_language|_and_pseudo-pelger-huet_anomaly": 15,
    "pseudo-Pelger-Huet_anomaly": 1,
    "not_provided|Poor_speech|Intellectual_disability|_severe|Abnormal_facial_shape|Absent_speech|Motor_delay|Neurodevelopmental_disorder_with_facial_dysmorphism|_absent_language|_and_pseudo-pelger-huet_anomaly": 1,
    "TMEM147-related_disorder": 2,
    "not_provided|Neurodevelopmental_disorder_with_facial_dysmorphism|_absent_language|_and_pseudo-pelger-huet_anomaly": 1,
    "not_provided|TMEM147-related_disorder": 1,
    "Heart|_malformation_of|Hypoplastic_left_heart_syndrome|Polydactyly|Abnormal_vertebral_morphology": 2,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_7": 1,
    "not_provided|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_7": 3,
    "not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_provided|COX6B1-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_7|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_7|not_specified|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_7": 3,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_7|not_specified": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_7|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_7|not_provided|Inborn_genetic_diseases": 1,
    "Dystonia_28|_childhood-onset|Intellectual_developmental_disorder|_autosomal_dominant_68|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Dystonia_28|_childhood-onset|Intellectual_developmental_disorder|_autosomal_dominant_68": 1,
    "KMT2B-related_disorder": 25,
    "Dystonia_28|_childhood-onset": 63,
    "Inborn_genetic_diseases|not_provided|KMT2B-related_disorder": 2,
    "Dystonia_28|_childhood-onset|Intellectual_developmental_disorder|_autosomal_dominant_68": 3,
    "Intellectual_developmental_disorder|_autosomal_dominant_68|Dystonia_28|_childhood-onset|not_provided|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Dystonia_28|_childhood-onset": 1,
    "Complex_neurodevelopmental_disorder_with_motor_features": 3,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_68|Dystonia_28|_childhood-onset": 1,
    "Dystonia_28|_childhood-onset|not_provided": 26,
    "not_provided|KMT2B-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Dystonia_28|_childhood-onset": 9,
    "Intellectual_developmental_disorder|_autosomal_dominant_68": 15,
    "not_provided|KMT2B-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_dominant_68|Dystonia_28|_childhood-onset": 1,
    "not_provided|Dystonia_28|_childhood-onset|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|KMT2B-related_disorder": 4,
    "KMT2B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Dystonia_28|_childhood-onset|See_cases|not_provided": 1,
    "not_provided|Dystonia_28|_childhood-onset|KMT2B-related_disorder": 1,
    "not_provided|KMT2B-related_disorder": 12,
    "KMT2B-related_disorder|not_provided": 22,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_5": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_68|Dystonia_28|_childhood-onset|not_provided|KMT2B-related_disorder": 1,
    "Intellectual_disability|KMT2B-related_disorder|not_provided": 1,
    "Dystonia_28|_childhood-onset|not_provided|KMT2B-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_68|Dystonia_28|_childhood-onset": 4,
    "KMT2B-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Intellectual_disability|Dystonia_28|_childhood-onset|not_provided": 1,
    "Specific_learning_disability|Dystonic_disorder|Myoclonus|Dysarthria|Abnormality_of_metabolism/homeostasis": 1,
    "Dystonia_28|_childhood-onset|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Dystonia_28|_childhood-onset|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_developmental_disorder|_autosomal_dominant_68": 2,
    "Dystonia_28|_childhood-onset|Intellectual_developmental_disorder|_autosomal_dominant_68|not_provided": 1,
    "KMT2B-related_disorder|Dystonia_28|_childhood-onset|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Dystonia_28|_childhood-onset": 1,
    "Generalized_dystonia|Poor_motor_coordination|Dysarthria|Dystonia_28|_childhood-onset": 1,
    "KMT2B-related_disorder|Intellectual_developmental_disorder|_autosomal_dominant_68|Dystonia_28|_childhood-onset|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|See_cases": 1,
    "Generalized_dystonia|Dysarthria": 1,
    "KMT2B-related_disorder|Inborn_genetic_diseases": 1,
    "PSENEN-related_disorder": 1,
    "Acne_inversa|_familial|_2": 8,
    "not_provided|Acne_inversa|_familial|_2": 1,
    "PRODH2-related_disorder": 7,
    "Congenital_nephrotic_syndrome": 33,
    "Congenital_nephrotic_syndrome|not_provided": 15,
    "Finnish_congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 6,
    "Finnish_congenital_nephrotic_syndrome|not_provided": 123,
    "Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases": 13,
    "Finnish_congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|not_provided": 2,
    "not_specified|Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "not_provided|Finnish_congenital_nephrotic_syndrome": 129,
    "not_provided|Finnish_congenital_nephrotic_syndrome|NPHS1-related_disorder|not_specified": 1,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Kidney_disorder": 1,
    "Congenital_nephrotic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "NPHS1-related_disorder": 7,
    "Congenital_nephrotic_syndrome|NPHS1-related_disorder|not_provided": 1,
    "not_provided|Focal_segmental_glomerulosclerosis|not_specified|Finnish_congenital_nephrotic_syndrome": 1,
    "not_specified|Finnish_congenital_nephrotic_syndrome|not_provided": 3,
    "Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases|not_provided|Nephrotic_syndrome": 1,
    "NPHS1-related_disorder|not_provided": 3,
    "Congenital_nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 7,
    "Congenital_nephrotic_syndrome|Inborn_genetic_diseases|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|not_specified|not_provided": 2,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis|Finnish_congenital_nephrotic_syndrome": 1,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided": 5,
    "NPHS1-related_disorder|not_provided|Finnish_congenital_nephrotic_syndrome": 6,
    "not_provided|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_specified": 1,
    "NPHS1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Finnish_congenital_nephrotic_syndrome": 3,
    "Nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 3,
    "Finnish_congenital_nephrotic_syndrome|not_provided|NPHS1-related_disorder": 3,
    "not_provided|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "not_provided|NPHS1-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Finnish_congenital_nephrotic_syndrome": 3,
    "Familial_idiopathic_steroid-resistant_nephrotic_syndrome|not_provided|Congenital_nephrotic_syndrome|NPHS1-related_disorder": 1,
    "not_specified|not_provided|Finnish_congenital_nephrotic_syndrome": 6,
    "Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases|NPHS1-related_disorder|Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|not_provided|Finnish_congenital_nephrotic_syndrome": 2,
    "NPHS1-related_disorder|not_provided|Kidney_disorder": 1,
    "Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Congenital_nephrotic_syndrome": 3,
    "not_provided|Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|not_specified|Finnish_congenital_nephrotic_syndrome": 2,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided|NPHS1-related_disorder": 1,
    "not_provided|NPHS1-related_disorder|Finnish_congenital_nephrotic_syndrome|Nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|Congenital_nephrotic_syndrome": 3,
    "Finnish_congenital_nephrotic_syndrome|Proteinuria|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome": 2,
    "not_provided|NPHS1-related_disorder|Kidney_disorder|Finnish_congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Finnish_congenital_nephrotic_syndrome|NPHS1-related_disorder|Kidney_disorder|not_specified|Congenital_nephrotic_syndrome|not_provided": 1,
    "not_specified|not_provided|Nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 1,
    "Congenital_nephrotic_syndrome|Inborn_genetic_diseases": 2,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Focal_segmental_glomerulosclerosis": 2,
    "Nephrotic_syndrome|See_cases|Finnish_congenital_nephrotic_syndrome|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|not_specified|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|not_provided|not_specified": 3,
    "not_provided|Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "NPHS1-related_disorder|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_nephrotic_syndrome": 2,
    "Focal_segmental_glomerulosclerosis|Finnish_congenital_nephrotic_syndrome": 1,
    "Nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided": 5,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "NPHS1-related_disorder|Finnish_congenital_nephrotic_syndrome|not_provided": 3,
    "Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome": 3,
    "not_provided|Nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 1,
    "not_provided|Finnish_congenital_nephrotic_syndrome|Familial_idiopathic_steroid-resistant_nephrotic_syndrome": 1,
    "Glomerulonephritis|Inborn_genetic_diseases|Finnish_congenital_nephrotic_syndrome": 1,
    "Congenital_nephrotic_syndrome|not_provided|NPHS1-related_disorder": 1,
    "not_specified|Finnish_congenital_nephrotic_syndrome|not_provided|Congenital_nephrotic_syndrome": 1,
    "not_provided|Finnish_congenital_nephrotic_syndrome|not_specified|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "not_provided|Congenital_nephrotic_syndrome|Inborn_genetic_diseases": 1,
    "Infantile_Nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Congenital_nephrotic_syndrome|not_specified": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Congenital_nephrotic_syndrome|not_specified|Finnish_congenital_nephrotic_syndrome": 1,
    "Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_provided|Finnish_congenital_nephrotic_syndrome": 2,
    "Congenital_and_infantile_nephrotic_syndrome": 1,
    "not_provided|Finnish_congenital_nephrotic_syndrome|not_specified": 3,
    "Finnish_congenital_nephrotic_syndrome|not_specified": 2,
    "Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|not_provided": 2,
    "Nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome|NPHS1-related_disorder": 1,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Proteinuria": 1,
    "Nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 2,
    "Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided|not_specified": 1,
    "Infantile_Nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided": 1,
    "Finnish_congenital_nephrotic_syndrome|NPHS1-related_disorder|not_provided": 3,
    "not_provided|Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|NPHS1-related_disorder": 1,
    "Proteinuria|NPHS1-related_disorder|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "NPHS1-related_disorder|Microscopic_hematuria|Finnish_congenital_nephrotic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Kidney_disorder|Nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "Inborn_genetic_diseases|Finnish_congenital_nephrotic_syndrome|not_provided": 3,
    "Proteinuria|not_provided|Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_specified": 1,
    "not_provided|not_specified|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 1,
    "Congenital_nephrotic_syndrome|Proteinuria": 1,
    "not_specified|Congenital_nephrotic_syndrome|Atypical_hemolytic-uremic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "not_specified|not_provided|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "not_specified|not_provided|Finnish_congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome": 1,
    "not_specified|Finnish_congenital_nephrotic_syndrome": 3,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "NPHS1-related_disorder|not_provided|Finnish_congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "NPHS1-related_disorder|Finnish_congenital_nephrotic_syndrome": 1,
    "not_provided|NPHS1-related_disorder": 1,
    "not_provided|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 1,
    "Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_specified|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 2,
    "not_specified|not_provided|Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "Finnish_congenital_nephrotic_syndrome|Nephrotic_syndrome": 1,
    "NPHS1-related_disorder|Microscopic_hematuria|not_provided|Inborn_genetic_diseases|Finnish_congenital_nephrotic_syndrome": 1,
    "not_provided|Finnish_congenital_nephrotic_syndrome|not_specified|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "not_provided|NPHS1-related_disorder|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|not_provided|Nephrotic_syndrome|NPHS1-related_disorder": 1,
    "Finnish_congenital_nephrotic_syndrome|NPHS1-related_disorder": 1,
    "Congenital_nephrotic_syndrome|not_specified|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "NPHS1-related_disorder|not_specified|not_provided|Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis": 1,
    "Finnish_congenital_nephrotic_syndrome|Steroid-resistant_nephrotic_syndrome|Nephrotic_range_proteinuria|Congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|not_provided|NPHS1-related_disorder": 1,
    "Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|Inborn_genetic_diseases": 2,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_nephrotic_syndrome": 1,
    "not_provided|Congenital_nephrotic_syndrome|not_specified|Finnish_congenital_nephrotic_syndrome": 1,
    "not_provided|Finnish_congenital_nephrotic_syndrome|Kidney_disorder": 1,
    "Congenital_nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome|not_specified": 1,
    "Infantile_Nephrotic_syndrome|Nephrotic_syndrome|not_provided|Finnish_congenital_nephrotic_syndrome": 1,
    "Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_specified|not_provided": 1,
    "Finnish_congenital_nephrotic_syndrome|Congenital_nephrotic_syndrome|Focal_segmental_glomerulosclerosis|not_provided|NPHS1-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_nephrotic_syndrome|Finnish_congenital_nephrotic_syndrome": 1,
    "TYROBP-related_disorder|not_provided": 2,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1|not_provided": 3,
    "TYROBP-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|TYROBP-related_disorder|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "Parkinsonian_disorder|Dementia|Frontotemporal_cerebral_atrophy|Caudate_atrophy|Action_tremor|Cerebellar_atrophy|Bradykinesia|Cerebral_cortical_atrophy|Memory_impairment|not_provided": 1,
    "TYROBP-related_disorder|not_provided|Polycystic_lipomembranous_osteodysplasia_with_sclerosing_leukoencephalopathy_1": 1,
    "not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_2": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_2": 6,
    "Inborn_genetic_diseases|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 2,
    "not_provided|Mitochondrial_complex_2_deficiency|_nuclear_type_2|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_provided|SDHAF1-related_disorder": 1,
    "Mitochondrial_complex_2_deficiency|_nuclear_type_2|not_specified|not_provided": 1,
    "not_specified|Mitochondrial_complex_II_deficiency|_nuclear_type_1|not_provided": 1,
    "not_specified|not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_II_deficiency|_nuclear_type_1": 2,
    "not_specified|SYNE4-related_disorder|not_provided": 2,
    "SYNE4-related_disorder|not_specified|not_provided": 2,
    "not_specified|not_provided|SYNE4-related_disorder": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_76": 5,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_76": 4,
    "not_provided|SYNE4-related_disorder": 3,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_76": 1,
    "SYNE4-related_disorder|not_provided": 4,
    "SYNE4-related_disorder|not_provided|not_specified|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_76": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_76|not_provided": 6,
    "Autosomal_recessive_nonsyndromic_hearing_loss_76|Nonsyndromic_genetic_hearing_loss": 2,
    "not_provided|not_specified|SYNE4-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_76|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_76|Rare_genetic_deafness|not_provided": 1,
    "SYNE4-related_hearing_loss|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_76|not_specified": 1,
    "not_provided|SYNE4-related_disorder|not_specified": 1,
    "Primary_Microcephaly_2_With_or_Without_Cortical_Malformations|Inborn_genetic_diseases|not_provided": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 113,
    "Inborn_genetic_diseases|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 5,
    "Inborn_genetic_diseases|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 2,
    "not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 31,
    "not_specified|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 17,
    "not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided": 3,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided": 22,
    "not_specified|not_provided|Inborn_genetic_diseases|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "WDR62-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|Autosomal_recessive_primary_microcephaly": 1,
    "Primary_Microcephaly_2_With_or_Without_Cortical_Malformations|not_specified|not_provided": 1,
    "WDR62-related_disorder|not_specified|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 2,
    "not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|Inborn_genetic_diseases": 3,
    "not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|WDR62-related_disorder": 1,
    "WDR62-related_disorder": 11,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified": 1,
    "not_provided|WDR62-related_disorder": 4,
    "not_provided|WDR62-related_disorder|Inborn_genetic_diseases": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|Inborn_genetic_diseases": 2,
    "WDR62-related_disorder|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided": 2,
    "not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified": 8,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|not_specified": 7,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified|not_provided": 5,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|Inborn_genetic_diseases": 2,
    "WDR62-related_disorder|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 2,
    "Inborn_genetic_diseases|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided": 2,
    "Primary_Microcephaly_2_With_or_Without_Cortical_Malformations|not_provided|not_specified": 2,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified|not_provided|WDR62-related_disorder": 1,
    "WDR62-related_disorder|not_provided": 9,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|WDR62-related_disorder": 1,
    "not_provided|Abnormal_cerebral_morphology|Inborn_genetic_diseases|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|Primary_microcephaly_type_2": 1,
    "WDR62-related_disorder|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_primary_microcephaly|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "not_provided|not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 4,
    "not_provided|WDR62-related_disorder|not_specified": 1,
    "Intellectual_disability|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|Intellectual_disability|not_specified|Inborn_genetic_diseases": 1,
    "WDR62-related_disorder|not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided": 1,
    "not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|WDR62-related_disorder|not_specified": 1,
    "WDR62-related_disorder|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified|not_provided": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|WDR62-related_disorder": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|Skraban-Deardorff_syndrome": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|Inborn_genetic_diseases|not_provided": 5,
    "WDR62-related_disorder|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|WDR62-related_disorder|not_specified": 1,
    "Primary_Microcephaly|_Recessive|Microcephaly|_cortical_malformations|_and_intellectual_disability|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 3,
    "not_provided|WDR62-related_disorder|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_specified": 1,
    "not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Skraban-Deardorff_syndrome": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|WDR62-related_disorder|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|WDR62-related_disorder|not_provided": 1,
    "not_specified|WDR62-related_disorder|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations|not_provided|Inborn_genetic_diseases|Intellectual_disability|not_specified": 1,
    "Microcephaly|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "Intellectual_disability|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "WDR62-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|Microcephaly_2|_primary|_autosomal_recessive|_with_or_without_cortical_malformations": 1,
    "not_specified|NEURODEVELOPMENTAL_DISORDER_WITH_BEHAVIORAL_ABNORMALITIES_AND_CHILDHOOD-ONSET_SPASTIC_PARAPLEGIA": 1,
    "Pulmonary_hypertension|_primary|_6": 2,
    "Focal_segmental_glomerulosclerosis_4|_susceptibility_to": 5,
    "not_provided|SIPA1L3-related_disorder": 10,
    "SIPA1L3-related_disorder|not_provided": 10,
    "Cataract_45": 9,
    "SIPA1L3-related_disorder": 7,
    "Cataract_45|not_specified|not_provided": 1,
    "Cataract_45|not_provided": 2,
    "Congenital_secretory_sodium_diarrhea_3": 11,
    "not_provided|SPINT2-related_disorder": 5,
    "Congenital_secretory_sodium_diarrhea_3|not_provided": 3,
    "Congenital_sodium_diarrhea|not_provided": 1,
    "Congenital_secretory_sodium_diarrhea_3|Congenital_sodium_diarrhea|not_provided": 1,
    "SPINT2-related_disorder|not_provided": 2,
    "YIF1B-related_condition": 1,
    "Kaya-Barakat-Masson_syndrome": 5,
    "Kaya-Barakat-Masson_syndrome|not_provided": 2,
    "Kaya-Barakat-Masson_syndrome|Inborn_genetic_diseases": 1,
    "GGN-related_disorder|not_provided": 2,
    "Spermatogenic_failure_69": 2,
    "FAM98C-related_disorder": 8,
    "not_specified|FAM98C-related_disorder": 1,
    "not_provided|FAM98C-related_disorder": 1,
    "Autism_spectrum_disorder|Asphyxiating_thoracic_dystrophy_3": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 11,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 3,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 2,
    "Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 2,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 4,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 5,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 7,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 6,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 4,
    "not_provided|RYR1-related_disorder": 183,
    "RYR1-related_disorder": 3824,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 83,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 427,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 47,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 466,
    "RYR1-related_disorder|King_Denborough_syndrome|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 6,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 5,
    "not_provided|RYR1-related_disorder|not_specified": 13,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|RYR1-related_myopathy": 2,
    "Malignant_hyperthermia_of_anesthesia|not_provided": 27,
    "not_specified|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 8,
    "not_provided|RYR1-related_disorder|Inborn_genetic_diseases": 6,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 2,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 5,
    "RYR1-related_disorder|not_provided": 240,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "not_provided|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 16,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 43,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 49,
    "not_provided|Inborn_genetic_diseases|RYR1-related_disorder": 7,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia": 32,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Central_core_disease|_autosomal_recessive|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_specified": 55,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 4,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 5,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "not_specified|RYR1-related_disorder": 45,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 10,
    "RYR1-related_myopathy|RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 4,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 10,
    "RYR1-related_disorder|not_specified|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 54,
    "King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_specified|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_provided|Centronuclear_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|RYR1-related_disorder": 11,
    "not_specified|not_provided|RYR1-related_disorder": 6,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 6,
    "RYR1-related_myopathy": 16,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 67,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder": 3,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Myopathy": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 54,
    "RYR1-related_myopathy|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "not_specified|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 3,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 7,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 77,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|desflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "not_specified|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 3,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 2,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|RYR1-related_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "not_provided|RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_myopathy|RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "not_provided|King_Denborough_syndrome|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Myopathy|_RYR1-associated": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 16,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 5,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 4,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 6,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 4,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 3,
    "RYR1-related_disorder|Malignant_hypothermia|not_specified|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 5,
    "RYR1-related_disorder|Autism_spectrum_disorder_due_to_AUTS2_deficiency|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases": 34,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|RYR1-related_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 2,
    "RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion": 3,
    "RYR1-related_disorder|Central_core_myopathy": 10,
    "RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_specified|RYR1-related_disorder|not_provided|Respiratory_insufficiency|Myopathy|Congenital_muscular_dystrophy": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 2,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome": 4,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|not_provided": 1,
    "not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|not_specified|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 2,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_provided|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1": 8,
    "RYR1-related_disorder|Neuromuscular_disease|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|RYR1-related_myopathy|Malignant_hyperthermia_of_anesthesia|not_specified|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "RYR1-related_myopathy|not_provided|RYR1-related_disorder": 1,
    "Central_core_myopathy|RYR1-related_disorder|not_provided": 3,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 2,
    "RYR1-related_disorder|not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 2,
    "Central_core_myopathy": 60,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|RYR1-related_myopathy|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_specified|not_provided": 1,
    "Congenital_muscular_dystrophy|Respiratory_insufficiency|Myopathy": 1,
    "RYR1-related_disorder|not_specified|not_provided": 13,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|not_provided|RYR1-related_disorder": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity|Central_core_myopathy|not_provided|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Myopathy|_RYR1-associated|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|See_cases|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Elevated_circulating_creatine_kinase_concentration|Myalgia|Exercise-induced_myalgia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases": 4,
    "not_provided|not_specified|RYR1-related_disorder": 3,
    "not_provided|RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1": 3,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided|RYR1-related_disorder|Centronuclear_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 2,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided": 1,
    "not_provided|Central_core_myopathy|not_specified": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|not_provided|King_Denborough_syndrome|Central_core_myopathy": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_specified|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 7,
    "Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_specified|not_provided": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_provided|Multiminicore_myopathy|Autosomal_dominant_centronuclear_myopathy": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 6,
    "Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 16,
    "Inborn_genetic_diseases|not_provided|Central_core_myopathy": 1,
    "RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 6,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder": 2,
    "RYR1-related_disorder|not_specified|not_provided|Central_core_myopathy": 1,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_provided": 1,
    "not_provided|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Centronuclear_myopathy": 4,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|not_provided": 2,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder": 2,
    "Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|not_provided|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_specified|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|RYR1-related_disorder|RYR1-related_myopathy|not_provided": 1,
    "Myopathy|_RYR1-associated|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 2,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|not_specified": 1,
    "RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 11,
    "not_provided|Malignant_hyperthermia_of_anesthesia": 4,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 3,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_provided|succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_provided|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity": 1,
    "Myopathy|RYR1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1": 6,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 4,
    "Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Malignant_hyperthermia_of_anesthesia|not_specified|Multiminicore_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_provided|not_specified": 8,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|RYR1-related_disorder": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "Inborn_genetic_diseases|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 3,
    "not_specified|RYR1-related_disorder|Inborn_genetic_diseases": 2,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 1,
    "Multiminicore_myopathy|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Congenital_myopathy|not_specified|not_provided": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Inborn_genetic_diseases|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Myopathy|_RYR1-associated|not_provided|not_specified": 1,
    "RYR1-related_disorder|not_provided|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1": 5,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 2,
    "not_provided|RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|RYR1-related_disorder": 10,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_myopathy|not_provided": 1,
    "Rhabdomyolysis-myalgia_syndrome": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Central_core_myopathy|Inborn_genetic_diseases": 2,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|not_specified": 1,
    "RYR1-related_disorder|Malignant_hypothermia|not_provided": 1,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "not_provided|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "not_specified|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 7,
    "Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder": 1,
    "Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy": 1,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 3,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Autosomal_dominant_centronuclear_myopathy|Central_core_myopathy|not_provided": 1,
    "Centronuclear_myopathy|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Myopathy|not_provided|RYR1-related_disorder": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 4,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 6,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|Inborn_genetic_diseases|Epilepsy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_myopathy|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1": 10,
    "not_specified|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 3,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 2,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided": 2,
    "not_specified|RYR1-related_myopathy": 1,
    "Central_core_myopathy|not_specified|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|Myopathy|_RYR1-associated|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Myopathy": 1,
    "not_provided|Central_core_myopathy": 9,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 2,
    "RYR1-related_disorder|RYR1-related_myopathy|not_specified|Congenital_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_myopathy|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_specified|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Central_core_myopathy": 1,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Inborn_genetic_diseases|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|RYR1-related_disorder": 4,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome": 1,
    "Malignant_hyperthermia_and_exertional_rhabdomyolosis|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 5,
    "Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder": 3,
    "Inborn_genetic_diseases|RYR1-related_disorder": 21,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 13,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome": 2,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome": 1,
    "Inborn_genetic_diseases|RYR1-related_myopathy|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_provided|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Congenital_myopathy|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|not_provided|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "RYR1-related_disorder|Multiminicore_myopathy|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia": 1,
    "RYR1-related_disorder|not_specified|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 4,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Multiminicore_myopathy|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Malignant_hyperthermia_of_anesthesia": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 2,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "not_specified|RYR1-related_disorder|not_provided": 3,
    "Inborn_genetic_diseases|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder|not_provided": 1,
    "not_specified|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|not_provided|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_specified|not_provided": 2,
    "not_specified|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 4,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder": 4,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "not_provided|Mildly_elevated_creatine_kinase|Limb_pain|Myotonia|Osteoporosis|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|RYR1-related_disorder|not_provided|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "not_provided|Centronuclear_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|Arthrogryposis_multiplex_congenita|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome": 1,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Inborn_genetic_diseases|Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_specified|RYR1-related_disorder|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Myopathy|_RYR1-associated|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome": 2,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified|Multiminicore_myopathy|not_provided": 1,
    "RYR1-related_disorder|Myopathy": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder": 3,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_specified|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|not_specified|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder": 1,
    "Centronuclear_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Delayed_gross_motor_development|Pelvic_girdle_muscle_weakness|Progressive_distal_muscle_weakness|Proximal_muscle_weakness|Scoliosis": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_skeletal_muscle_disorder|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_myopathy|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|Inborn_genetic_diseases|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder": 3,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 3,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|Myopathy|_RYR1-associated|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "RYR1-related_disorder|Myopathy|_RYR1-associated|not_provided|Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 4,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified": 8,
    "Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Centronuclear_myopathy|not_provided|RYR1-related_disorder": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 7,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|not_specified": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 2,
    "Malignant_hyperthermia_of_anesthesia|not_provided|RYR1-related_disorder": 3,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|not_specified|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|not_specified|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|not_specified|Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myasthenic_syndrome|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Inborn_genetic_diseases|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder|Hypotonia": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_specified|Malignant_hyperthermia_of_anesthesia|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Inborn_genetic_diseases|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Central_core_myopathy": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_myopathy|not_provided|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_disorder": 1,
    "Congenital_myasthenic_syndrome|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 2,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 5,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified|not_provided|Multiminicore_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 4,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|RYR1-related_myopathy": 1,
    "Malignant_hyperthermia_equivocal_with_halotane|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Neuromuscular_disease|Congenital_myopathy|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|See_cases|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia": 1,
    "Inborn_genetic_diseases|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_specified|not_provided|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 5,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 2,
    "King_Denborough_syndrome": 4,
    "RYR1-related_myopathy|RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Anterior_segment_dysgenesis_7|not_specified|not_provided|See_cases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|not_provided|RYR1-related_myopathy": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|Multiminicore_myopathy": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 4,
    "not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 4,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 8,
    "Centronuclear_myopathy|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "RYR1-related_disorder|not_provided|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|not_specified|Malignant_hypothermia|Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided": 4,
    "RYR1-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 1,
    "not_specified|RYR1-related_disorder|RYR1-related_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases|not_provided": 1,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases": 2,
    "Malignant_hypothermia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Myalgia|Exercise-induced_myalgia|Elevated_circulating_creatine_kinase_concentration|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|not_specified|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases": 1,
    "Long_QT_syndrome|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 5,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided": 1,
    "Central_core_myopathy|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Myopathy|_RYR1-associated|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Autosomal_dominant_centronuclear_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Multiminicore_myopathy": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Central_core_myopathy": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_provided": 3,
    "Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "Central_core_myopathy|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|RYR1-related_disorder|not_provided": 2,
    "Centronuclear_myopathy|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|RYR1-related_disorder": 8,
    "RYR1-related_disorder|not_provided|not_specified|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|not_provided": 13,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 3,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 4,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "Central_core_myopathy|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia_of_anesthesia|not_specified|Multiminicore_myopathy|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|Multiminicore_myopathy|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Inborn_genetic_diseases|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Myopathy|_RYR1-associated|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Multiminicore_myopathy|Central_core_myopathy|not_provided": 1,
    "not_provided|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_provided|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "not_specified|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hypothermia": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|not_provided|Multiminicore_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided": 1,
    "not_specified|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_specified": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|not_specified": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "not_specified|Central_core_myopathy|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_and_exertional_rhabdomyolosis|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|RYR1-related_disorder": 7,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity": 1,
    "not_specified|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "RYR1-related_myopathy|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Central_core_myopathy": 1,
    "not_provided|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_provided|History_of_neonatal_hypotonia|Absence_of_the_sacrum|Ptosis": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|not_provided": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|Central_core_myopathy|RYR1-related_disorder": 2,
    "RYR1-related_disorder|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified": 1,
    "not_specified|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Central_core_myopathy|Neuromuscular_disease|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Multi-minicore_disease_and_atypical_periodic_paralysis|not_provided|Hydrops_fetalis": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|Multiminicore_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia_of_anesthesia": 1,
    "Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified|Multiminicore_myopathy|not_provided": 1,
    "Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 2,
    "Central_core_myopathy|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Centronuclear_myopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 1,
    "Centronuclear_myopathy|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_myopathy|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Centronuclear_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|Central_core_disease|_autosomal_recessive|Centronuclear_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder": 1,
    "Inborn_genetic_diseases|Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "RYR1-related_myopathy|not_provided|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|sevoflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 3,
    "Hereditary_skeletal_muscle_disorder|RYR1-related_myopathy|Inborn_genetic_diseases|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Centronuclear_myopathy": 1,
    "not_specified|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 2,
    "Centronuclear_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 5,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 2,
    "Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_myopathy|not_provided|Centronuclear_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Central_core_myopathy|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided|Congenital_contracture|Proximal_amyotrophy|Delayed_gross_motor_development|Short_stature": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Inborn_genetic_diseases|not_provided|RYR1-related_disorder": 1,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 2,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_specified|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_specified|not_provided": 1,
    "not_specified|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|Neuromuscular_disease|not_provided|Clubfoot|EMG_abnormality|Lower_limb_amyotrophy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|not_provided|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1|not_provided|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Inborn_genetic_diseases|not_provided|succinylcholine_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Malignant_hyperthermia_of_anesthesia": 1,
    "not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|King_Denborough_syndrome|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|succinylcholine_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|succinylcholine_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|not_provided": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|King_Denborough_syndrome|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Abnormality_of_the_musculature": 1,
    "not_provided|RYR1-related_disorder|desflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Central_core_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "not_specified|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "not_provided|RYR1-related_disorder|Inborn_genetic_diseases|Central_core_myopathy": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|not_specified|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Multiminicore_myopathy|not_specified|Malignant_hyperthermia_of_anesthesia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified": 1,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_specified|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided|Central_core_myopathy|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 2,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome": 1,
    "Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Inborn_genetic_diseases": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "RYR1-related_disorder|Inborn_genetic_diseases|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided": 3,
    "not_provided|Long_QT_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_specified": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 4,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided|Central_core_myopathy": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Inborn_genetic_diseases|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder": 2,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|not_specified": 1,
    "not_provided|RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia": 1,
    "not_specified|not_provided|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 2,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 4,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 3,
    "RYR1-related_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 2,
    "RYR1-related_disorder|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Centronuclear_myopathy|RYR1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_myopathy": 1,
    "RYR1-related_disorder|Malignant_hypothermia|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Myopathy|_RYR1-associated|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder|King_Denborough_syndrome|not_provided|not_specified": 1,
    "King_Denborough_syndrome|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_myopathy": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Myopathy|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|King_Denborough_syndrome|not_provided|Central_core_myopathy": 1,
    "not_specified|King_Denborough_syndrome|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|not_provided": 1,
    "Central_core_myopathy|not_specified|not_provided|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|King_Denborough_syndrome|Central_core_myopathy": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 4,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Centronuclear_myopathy|RYR1-related_myopathy|not_provided|Abnormality_of_the_musculature": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion": 2,
    "King_Denborough_syndrome|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Multiminicore_myopathy|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 2,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|not_provided|RYR1-related_myopathy|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "RYR1-related_disorder|not_provided|RYR1-related_myopathy": 1,
    "Malignant_hyperthermia_of_anesthesia|not_provided|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_myopathy|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Myopathy|_RYR1-associated|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|not_specified|not_provided|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Multiminicore_myopathy|RYR1-related_disorder|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia": 1,
    "RYR1-related_disorder|Malignant_hypothermia|Malignant_hyperthermia_of_anesthesia|not_provided|Long_QT_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|RYR1-related_disorder|succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "not_specified|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_myopathy|Inborn_genetic_diseases": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Central_core_myopathy": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Multiminicore_myopathy|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|See_cases": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|not_specified|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Fetal_akinesia_deformation_sequence_1|Arthrogryposis_multiplex_congenita": 1,
    "Inborn_genetic_diseases|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided": 1,
    "RYR1-related_disorder|RYR1-related_myopathy": 1,
    "RYR1-related_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Inborn_genetic_diseases|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 5,
    "Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 2,
    "Inborn_genetic_diseases|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Axial_myopathy|_late-onset|not_specified|not_provided|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Inborn_genetic_diseases|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy": 3,
    "RYR1-related_disorder|Congenital_myopathy|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|Central_core_myopathy": 1,
    "RYR1-related_disorder|RYR1-related_myopathy|Congenital_myasthenic_syndrome_12|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|not_specified": 2,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|not_provided|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia_of_anesthesia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Abnormality_of_the_musculature": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_specified|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia_of_anesthesia|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Inborn_genetic_diseases": 1,
    "Centronuclear_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_specified": 1,
    "not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Arthrogryposis_multiplex_congenita|Fetal_akinesia_deformation_sequence_1": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Inborn_genetic_diseases|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|RYR1-related_disorder|RYR1-related_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified|Multiminicore_myopathy": 1,
    "not_provided|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "RYR1-related_myopathy|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Multiminicore/minicore/multicore_disease|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided|See_cases": 1,
    "RYR1-related_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "RYR1-related_disorder|not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|RYR1-related_disorder|not_specified": 1,
    "not_specified|Congenital_myopathy_with_fiber_type_disproportion|not_provided|RYR1-related_myopathy|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided|King_Denborough_syndrome|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "RYR1-related_disorder|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 2,
    "not_provided|RYR1-related_myopathy|Inborn_genetic_diseases|RYR1-related_disorder|Central_core_myopathy": 1,
    "not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder|RYR1-related_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_myopathy|Inborn_genetic_diseases|Myopathy|_RYR1-associated|not_provided|Centronuclear_myopathy": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_provided|Multiminicore_myopathy|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|Inborn_genetic_diseases|RYR1-related_disorder": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Central_core_myopathy|not_provided": 5,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "not_provided|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 3,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "not_provided|Central_core_disease|_autosomal_recessive": 1,
    "not_provided|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder": 1,
    "not_provided|Myopathy|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_specified": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 3,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "RYR1-related_disorder|RYR1-related_myopathy|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "Axial_myopathy|_late-onset|RYR1-related_disorder|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder|not_provided|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Malignant_hypothermia|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder": 2,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Malignant_hypothermia|not_specified|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder|not_specified|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 3,
    "not_specified|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided": 1,
    "Inborn_genetic_diseases|RYR1-related_myopathy": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_disorder|Malignant_hypothermia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_specified": 1,
    "RYR1-related_disorder|not_provided|Myopathy|_RYR1-associated|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Multiminicore_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_specified|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|See_cases": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_myopathy|RYR1-related_disorder|not_provided|Central_core_myopathy": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|Neuromuscular_disease|Malignant_hyperthermia_of_anesthesia|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|Scoliosis|Pelvic_girdle_muscle_weakness|Delayed_gross_motor_development|Proximal_muscle_weakness|Progressive_distal_muscle_weakness": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hypothermia|not_provided|RYR1-related_disorder": 1,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "not_specified|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_provided|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|not_specified|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome": 3,
    "Multiminicore_myopathy|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Muscular_dystrophy_and_arthrogryposis|not_specified": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Centronuclear_myopathy|RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Elevated_circulating_creatine_kinase_concentration|Myalgia|Exercise-induced_myalgia|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Inborn_genetic_diseases|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|RYR1-related_disorder|not_provided": 1,
    "Multiminicore_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Inborn_genetic_diseases|Congenital_myopathy|not_provided": 1,
    "RYR1-related_myopathy|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|not_specified|not_provided|See_cases": 1,
    "Inborn_genetic_diseases|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "RYR1-related_myopathy|not_provided|RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "Malignant_hyperthermia_of_anesthesia|not_provided|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|Malignant_hyperthermia|_susceptibility_to|_1|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "not_provided|not_specified|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_specified": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|RYR1-related_myopathy|not_provided": 1,
    "not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Centronuclear_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases": 1,
    "Multiminicore_myopathy|RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Congenital_myopathy|not_specified|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome": 1,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided|RYR1-related_disorder": 2,
    "RYR1-related_disorder|not_provided|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|not_provided|Central_core_myopathy": 5,
    "not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Distal_myopathy|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|RYR1-related_disorder": 1,
    "Multiminicore_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|not_specified": 1,
    "Multiminicore_myopathy|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|not_provided|not_specified|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_specified|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|not_provided|RYR1-related_disorder": 1,
    "Epilepsy|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_specified": 2,
    "RYR1-related_disorder|RYR1-related_myopathy|not_provided": 2,
    "Limb-girdle_muscular_dystrophy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 2,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_specified|not_provided|Limb-girdle_muscular_dystrophy": 1,
    "RYR1-related_disorder|Multiminicore_myopathy|not_provided|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided": 2,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|King_Denborough_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Multiminicore_myopathy|Myopathy|_RYR1-associated|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Inborn_genetic_diseases|not_provided": 1,
    "King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Intellectual_disability|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder": 2,
    "Multiminicore_myopathy|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Inborn_genetic_diseases|RYR1-related_disorder": 1,
    "not_specified|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Multiminicore_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Inborn_genetic_diseases|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Inborn_genetic_diseases|not_specified|not_provided|RYR1-related_disorder": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "RYR1-related_disorder|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_specified|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Central_core_myopathy|not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|not_specified|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Malignant_hyperthermia_of_anesthesia|Multiminicore_myopathy": 2,
    "not_provided|RYR1-related_disorder|Multiminicore_myopathy|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Inborn_genetic_diseases|not_provided|RYR1-related_disorder": 2,
    "Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy": 1,
    "Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|Multiminicore_myopathy|not_provided|not_specified|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|not_provided": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_myopathy|RYR1-related_disorder|not_provided": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_specified|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "not_specified|RYR1-related_disorder|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hypothermia|RYR1-related_disorder|Congenital_myopathy|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|Myopathy|_progressive_axial_with_cataracts|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided|EMG:_myopathic_abnormalities|Congenital_hip_dislocation|Congenital_muscular_dystrophy|Generalized_muscle_weakness": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "not_provided|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_specified|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "Malignant_hyperthermia_of_anesthesia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided|Centronuclear_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hypothermia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Inborn_genetic_diseases|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|not_provided": 1,
    "not_provided|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Central_core_myopathy": 1,
    "Central_core_myopathy|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|RYR1-related_disorder": 2,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Malignant_hyperthermia_of_anesthesia|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|RYR1-related_disorder|not_specified": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|not_provided|Central_core_myopathy": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Congenital_myopathy|not_provided|Abnormality_of_the_musculature": 1,
    "RYR1-related_disorder|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 2,
    "not_provided|Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_specified|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_specified|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia": 1,
    "not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided": 1,
    "Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|RYR1-related_myopathy|RYR1-related_disorder": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|King_Denborough_syndrome|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|not_specified|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Central_core_myopathy": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided": 1,
    "not_specified|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Inborn_genetic_diseases|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 2,
    "Central_core_myopathy|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Inborn_genetic_diseases|RYR1-related_disorder|not_specified|not_provided": 1,
    "Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|RYR1-related_disorder|Central_core_myopathy|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_myopathy|Central_core_myopathy|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_provided|RYR1-related_disorder": 1,
    "Malignant_hyperthermia_of_anesthesia|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome": 1,
    "succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder": 1,
    "RYR1-related_disorder|RYR1-related_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|not_specified|not_provided|Abnormality_of_the_musculature": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Malignant_hyperthermia_of_anesthesia|RYR1-related_disorder|not_provided": 2,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|Abnormality_of_the_musculature": 1,
    "Congenital_myopathy|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_disorder|Lynch_syndrome_5|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|not_provided": 1,
    "not_provided|RYR1-related_disorder|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|desflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity": 1,
    "RYR1-related_myopathy|not_provided": 2,
    "not_provided|desflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|sevoflurane_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|enflurane_response_-_Toxicity|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Congenital_myopathy_with_cores|Neuromuscular_disease|Malignant_hyperthermia_of_anesthesia|not_specified|not_provided": 1,
    "Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided": 1,
    "RYR1-related_myopathy|Inborn_genetic_diseases|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Centronuclear_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|enflurane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|See_cases": 1,
    "RYR1-related_disorder|RYR1-related_myopathy|Malignant_hyperthermia_of_anesthesia|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|methoxyflurane_response_-_Toxicity|halothane_response_-_Toxicity|isoflurane_response_-_Toxicity|desflurane_response_-_Toxicity|enflurane_response_-_Toxicity|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|not_provided|not_specified|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber": 1,
    "Inborn_genetic_diseases|not_specified|RYR1-related_disorder|not_provided|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "not_provided|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Congenital_myopathy_with_fiber_type_disproportion|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|not_specified|RYR1-related_disorder": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|not_provided": 1,
    "not_provided|Central_core_myopathy|RYR1-related_disorder": 2,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_provided|Central_core_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "RYR1-related_disorder|not_provided|Inborn_genetic_diseases|RYR1-related_myopathy": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_myopathy|not_provided|sevoflurane_response_-_Toxicity|succinylcholine_response_-_Toxicity|isoflurane_response_-_Toxicity|methoxyflurane_response_-_Toxicity|enflurane_response_-_Toxicity|halothane_response_-_Toxicity|desflurane_response_-_Toxicity": 1,
    "RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy": 1,
    "Congenital_muscular_dystrophy|EMG:_myopathic_abnormalities|Generalized_muscle_weakness|Congenital_hip_dislocation": 1,
    "Central_core_myopathy|not_provided|RYR1-related_disorder": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Congenital_myopathy_with_fiber_type_disproportion|King_Denborough_syndrome|See_cases|RYR1-related_disorder": 1,
    "RYR1-related_disorder|Neuromuscular_disease|_congenital|_with_uniform_type_1_fiber|not_provided": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion": 1,
    "King_Denborough_syndrome|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1": 1,
    "Malignant_hyperthermia_of_anesthesia|not_provided|Central_core_myopathy": 1,
    "RYR1-related_myopathy|RYR1-related_disorder|not_provided": 1,
    "RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|not_provided|Central_core_myopathy|Malignant_hyperthermia|_susceptibility_to|_1|See_cases": 1,
    "RYR1-related_disorder|Inborn_genetic_diseases|Malignant_hyperthermia_of_anesthesia|not_provided|Malignant_hyperthermia|_susceptibility_to|_1|Central_core_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "RYR1-related_myopathy|Congenital_multicore_myopathy_with_external_ophthalmoplegia|Malignant_hyperthermia|_susceptibility_to|_1|King_Denborough_syndrome|Central_core_myopathy|RYR1-related_disorder|not_provided|not_specified|Centronuclear_myopathy": 1,
    "Central_core_myopathy|not_provided|King_Denborough_syndrome|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_specified|Central_core_myopathy|King_Denborough_syndrome|Congenital_myopathy_with_fiber_type_disproportion|Congenital_multicore_myopathy_with_external_ophthalmoplegia|RYR1-related_disorder": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_myopathy": 1,
    "Malignant_hyperthermia|_susceptibility_to|_1|not_provided|RYR1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Malignant_hyperthermia_of_anesthesia|Congenital_multicore_myopathy_with_external_ophthalmoplegia": 1,
    "not_provided|Malignant_hyperthermia|_susceptibility_to|_1|RYR1-related_disorder|Central_core_myopathy": 1,
    "EIF3K_related_disorder": 1,
    "ACTN4-related_disorder": 25,
    "Focal_segmental_glomerulosclerosis|not_provided|Focal_segmental_glomerulosclerosis_1": 4,
    "Nephrotic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_1|not_provided|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_1|not_provided": 27,
    "not_provided|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_1|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_1|not_specified|not_provided": 2,
    "not_provided|Focal_segmental_glomerulosclerosis_1": 29,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_1|not_provided": 2,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_1|Focal_segmental_glomerulosclerosis": 3,
    "Focal_segmental_glomerulosclerosis_1|Inborn_genetic_diseases": 2,
    "not_provided|Focal_segmental_glomerulosclerosis_1|not_specified": 3,
    "Focal_segmental_glomerulosclerosis_1|ACTN4-related_disorder": 1,
    "Focal_segmental_glomerulosclerosis_1|Focal_segmental_glomerulosclerosis|not_provided|not_specified": 1,
    "not_specified|Focal_segmental_glomerulosclerosis_1|not_provided": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_1": 4,
    "Chronic_kidney_disease|Focal_segmental_glomerulosclerosis_1": 1,
    "Focal_segmental_glomerulosclerosis|not_provided|Intellectual_disability|_autosomal_dominant_14|not_specified|Focal_segmental_glomerulosclerosis_1": 1,
    "Focal_segmental_glomerulosclerosis_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Kidney_disorder|Focal_segmental_glomerulosclerosis_1": 1,
    "not_provided|ACTN4-related_disorder": 6,
    "ACTN4-related_disorder|Focal_segmental_glomerulosclerosis": 1,
    "ACTN4-related_disorder|not_provided": 3,
    "not_provided|Focal_segmental_glomerulosclerosis_1|ACTN4-related_disorder": 2,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_1": 3,
    "ACTN4-related_disorder|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_1": 1,
    "not_specified|Focal_segmental_glomerulosclerosis|not_provided|Focal_segmental_glomerulosclerosis_1": 1,
    "Inborn_genetic_diseases|not_provided|Focal_segmental_glomerulosclerosis_1": 2,
    "not_provided|not_specified|ACTN4-related_disorder": 1,
    "Inborn_genetic_diseases|Focal_segmental_glomerulosclerosis_1|ACTN4-related_disorder|not_provided": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_1": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_1|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Focal_segmental_glomerulosclerosis_1|Focal_segmental_glomerulosclerosis": 1,
    "Focal_segmental_glomerulosclerosis_1|ACTN4-related_disorder|not_provided": 1,
    "not_provided|Focal_segmental_glomerulosclerosis_1|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_1|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "ACTN4-related_disorder|Focal_segmental_glomerulosclerosis_1|not_provided": 2,
    "not_provided|Focal_segmental_glomerulosclerosis|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_1|not_provided|Inborn_genetic_diseases": 1,
    "Focal_segmental_glomerulosclerosis_1|not_provided|Focal_segmental_glomerulosclerosis": 1,
    "not_specified|not_provided|Focal_segmental_glomerulosclerosis_1": 1,
    "not_specified|Focal_segmental_glomerulosclerosis|Focal_segmental_glomerulosclerosis_1|not_provided": 1,
    "Kidney_disorder|Focal_segmental_glomerulosclerosis_1|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|not_specified|ACTN4-related_disorder|not_provided": 1,
    "CAPN12-related_disorder": 28,
    "not_provided|CAPN12-related_disorder": 4,
    "CAPN12-related_disorder|not_provided": 15,
    "CAPN12-related_disorder|not_specified|not_provided": 1,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 83,
    "SARS2-related_disorder|not_specified|not_provided": 2,
    "not_specified|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 3,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_specified|not_provided": 5,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_specified": 7,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_provided|SARS2-associated_condition": 1,
    "not_specified|SARS2-related_disorder|not_provided|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 1,
    "not_provided|not_specified|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 3,
    "not_specified|not_provided|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 4,
    "not_provided|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_specified": 4,
    "SARS2-associated_condition": 1,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_provided|not_specified": 3,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|SARS2-related_disorder|not_provided": 1,
    "SARS2-related_disorder|not_specified|not_provided|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome": 1,
    "SARS2-related_disorder|not_specified": 1,
    "SARS2-related_disorder": 1,
    "Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_provided|SARS2-related_disorder": 1,
    "not_specified|Hyperuricemia|_pulmonary_hypertension|_renal_failure|_alkalosis_syndrome|not_provided": 2,
    "SARS2-related_disorder|not_provided": 1,
    "not_provided|SARS2-related_disorder": 1,
    "MRPS12-related_disorder": 1,
    "peginterferon_alfa-2a_response_-_Efficacy|peginterferon_alfa-2b_response_-_Efficacy|ribavirin_response_-_Efficacy": 1,
    "not_specified|boceprevir|_peginterferon_alfa-2a|_peginterferon_alfa-2b_and_ribavirin_response_-_Efficacy|peginterferon_alfa-2a|_peginterferon_alfa-2b|_and_ribavirin_response_-_Efficacy|peginterferon_alfa-2a|_peginterferon_alfa-2b|_ribavirin|_and_telaprevir_response_-_Efficacy": 1,
    "not_provided|interferons|_peginterferon_alfa-2a|_peginterferon_alfa-2b|_and_ribavirin_response_-_Efficacy|peginterferon_alfa-2a|_peginterferon_alfa-2b|_ribavirin|_and_telaprevir_response_-_Efficacy": 1,
    "LRFN1": 1,
    "pontocerebellar_hypoplasia_with_cataract": 1,
    "Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B": 12,
    "PLEKHG2-related_disorder|not_provided": 11,
    "not_provided|PLEKHG2-related_disorder|not_specified": 1,
    "Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_provided": 8,
    "not_provided|Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|PLEKHG2-related_disorder": 1,
    "PLEKHG2-related_disorder": 3,
    "not_provided|PLEKHG2-related_disorder": 4,
    "not_provided|Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B": 2,
    "Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_specified": 3,
    "PLEKHG2-related_disorder|not_specified|not_provided": 1,
    "not_specified|Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B": 2,
    "not_specified|Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_provided": 1,
    "Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_specified|not_provided": 2,
    "not_specified|PLEKHG2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B": 1,
    "Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_provided|not_specified": 1,
    "SUPT5H-related_condition": 1,
    "TIMM50-related_disorder|not_provided": 2,
    "not_provided|TIMM50-related_disorder": 2,
    "3-methylglutaconic_aciduria_type_9": 5,
    "3-methylglutaconic_aciduria_type_9|Mitochondrial_encephalopathy": 2,
    "3-methylglutaconic_aciduria_type_9|TIMM50-related_disorder|not_provided": 1,
    "3-methylglutaconic_aciduria_type_9|not_provided": 8,
    "not_provided|3-methylglutaconic_aciduria_type_9|Mitochondrial_disease": 1,
    "not_provided|3-methylglutaconic_aciduria_type_9": 3,
    "not_provided|3-methylglutaconic_aciduria_type_9|Inborn_genetic_diseases": 1,
    "3-methylglutaconic_aciduria_type_9|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_9": 1,
    "TIMM50-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|3-methylglutaconic_aciduria_type_9|not_provided": 1,
    "Spondylocostal_dysostosis|Syndactyly": 1,
    "Syndactyly|Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|not_specified": 1,
    "not_provided|DLL3-related_disorder": 3,
    "not_provided|Syndactyly|Inborn_genetic_diseases|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive": 15,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided": 7,
    "not_specified|Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly|not_provided": 1,
    "not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly": 3,
    "not_provided|Inborn_genetic_diseases|Spondylocostal_dysostosis_1|_autosomal_recessive": 2,
    "Syndactyly|Spondylocostal_dysostosis_1|_autosomal_recessive": 9,
    "not_specified|Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided": 1,
    "not_provided|Syndactyly|Spondylocostal_dysostosis_1|_autosomal_recessive": 13,
    "not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 11,
    "not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly|DLL3-related_disorder|not_specified": 1,
    "not_provided|DLL3-related_disorder|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive|not_specified": 3,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_specified|Syndactyly|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Syndactyly|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive|Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_specified|Syndactyly": 1,
    "DLL3-related_disorder|not_provided": 2,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|Syndactyly|not_specified": 1,
    "Syndactyly|Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|DLL3-related_disorder": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly": 4,
    "Leukodystrophy_and_acquired_microcephaly_with_or_without_dystonia%3B|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "Syndactyly|Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided": 2,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Inborn_genetic_diseases|not_specified|not_provided|Syndactyly": 1,
    "Syndactyly|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 3,
    "Inborn_genetic_diseases|Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly": 2,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly|not_specified|not_provided": 1,
    "not_provided|Rib_fusion|Hemivertebrae": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|not_specified|Syndactyly": 2,
    "not_specified|Syndactyly|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Syndactyly|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly|DLL3-related_disorder|not_provided": 1,
    "Syndactyly|Inborn_genetic_diseases|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Inborn_genetic_diseases|not_provided|Syndactyly": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_specified|not_provided|Syndactyly": 1,
    "not_specified|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "DLL3-related_disorder": 2,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|Syndactyly|not_provided": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|DLL3-related_disorder": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|DLL3-related_disorder|not_provided|Syndactyly": 1,
    "not_specified|Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|Syndactyly": 1,
    "not_specified|Syndactyly|not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive": 1,
    "Syndactyly|Inborn_genetic_diseases|Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided": 1,
    "not_provided|Spondylocostal_dysostosis_1|_autosomal_recessive|DLL3-related_disorder|Syndactyly|not_specified": 1,
    "Spondylocostal_dysostosis_1|_autosomal_recessive|not_provided|Syndactyly": 1,
    "DYRK1B-related_disorder": 155,
    "DYRK1B-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|DYRK1B-related_disorder": 1,
    "not_provided|DYRK1B-related_disorder": 17,
    "Abdominal_obesity-metabolic_syndrome_3|Inborn_genetic_diseases|DYRK1B-related_disorder": 1,
    "Inborn_genetic_diseases|DYRK1B-related_disorder": 6,
    "Abdominal_obesity-metabolic_syndrome_3|DYRK1B-related_disorder": 1,
    "not_specified|DYRK1B-related_disorder|not_provided": 3,
    "DYRK1B-related_disorder|Abdominal_obesity-metabolic_syndrome_3": 3,
    "DYRK1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "DYRK1B-related_disorder|Inborn_genetic_diseases": 8,
    "Abdominal_obesity-metabolic_syndrome_3": 7,
    "Inborn_genetic_diseases|DYRK1B-related_disorder|Abdominal_obesity-metabolic_syndrome_3": 1,
    "DYRK1B-related_disorder|not_provided": 24,
    "Abdominal_obesity-metabolic_syndrome_3|Inborn_genetic_diseases": 1,
    "Abdominal_obesity-metabolic_syndrome_3|DYRK1B-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Abnormality_of_neuronal_migration|DYRK1B-related_disorder": 1,
    "Inborn_genetic_diseases|Abdominal_obesity-metabolic_syndrome_3": 1,
    "not_provided|Abdominal_obesity-metabolic_syndrome_3": 1,
    "not_provided|not_specified|DYRK1B-related_disorder": 1,
    "Abdominal_obesity-metabolic_syndrome_3|DYRK1B-related_disorder|not_provided": 1,
    "CCNP-related_disorder": 3,
    "AKT2-related_disorder": 5,
    "Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy": 98,
    "Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|not_specified": 2,
    "not_specified|Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy": 1,
    "Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|not_provided": 5,
    "Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus": 10,
    "not_provided|Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy": 4,
    "not_provided|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus": 1,
    "Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus|not_provided": 2,
    "Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus|Inborn_genetic_diseases": 1,
    "AKT2-related_disorder|not_provided|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus|not_specified": 2,
    "Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|AKT2-related_disorder": 4,
    "Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy": 2,
    "Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|AKT2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy": 1,
    "Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus|not_provided|not_specified": 1,
    "not_specified|Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Inborn_genetic_diseases": 1,
    "AKT2-related_disorder|Inborn_genetic_diseases|Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy": 1,
    "Type_2_diabetes_mellitus|Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|not_specified|AKT2-related_disorder": 1,
    "Hypoinsulinemic_hypoglycemia_and_body_hemihypertrophy|Type_2_diabetes_mellitus|not_specified|not_provided": 1,
    "PLD3-related_disorder": 3,
    "PLD3-related_disorder|not_provided": 2,
    "Spinocerebellar_ataxia_46": 5,
    "Alzheimer_disease_19|not_provided": 1,
    "not_provided|PLD3-related_disorder": 2,
    "Spinocerebellar_ataxia_46|not_specified": 1,
    "not_specified|Spinocerebellar_ataxia_46": 2,
    "Charcot-Marie-Tooth_disease_type_4F": 30,
    "not_provided|Charcot-Marie-Tooth_disease_type_4F": 2,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F": 2,
    "Charcot-Marie-Tooth_disease_type_4F|not_specified|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|not_provided": 1,
    "not_provided|Dejerine-Sottas_disease": 2,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|Tip-toe_gait|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_provided|Charcot-Marie-Tooth_disease_type_4": 3,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F": 4,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|Spinocerebellar_ataxia_46|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|_type_I|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_5": 1,
    "Inborn_genetic_diseases|not_specified|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_provided|PRX-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F": 8,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F": 4,
    "PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4": 5,
    "Charcot-Marie-Tooth_disease_type_4F|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4F": 4,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4": 4,
    "not_provided|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4": 1,
    "PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease_type_4|Progressive_peripheral_neuropathy|Progressive_gait_ataxia|Charcot-Marie-Tooth_disease_type_4F": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|Tip-toe_gait": 1,
    "not_provided|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Spinocerebellar_ataxia_46": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F|Tip-toe_gait": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease": 1,
    "PRX-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided|Autosomal_recessive_Dejerine-Sottas_syndrome|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Dejerine-Sottas_disease": 1,
    "Autosomal_recessive_Dejerine-Sottas_syndrome|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4F|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_specified|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_type_I|Charcot-Marie-Tooth_disease|Distal_spinal_muscular_atrophy": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_provided|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Tip-toe_gait|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|PRX-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4|Peripheral_neuropathy": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 5,
    "Charcot-Marie-Tooth_disease_type_4F|Autosomal_recessive_Dejerine-Sottas_syndrome|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "PRX-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases": 1,
    "PRX-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4": 2,
    "Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder": 1,
    "PRX-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 2,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F": 1,
    "not_specified|PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease": 1,
    "Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|not_provided": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_provided|Inborn_genetic_diseases": 1,
    "PRX-related_disorder|not_provided": 1,
    "PRX-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|PRX-related_disorder|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_type_4F|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_provided|PRX-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_specified|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Inborn_genetic_diseases|PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|_type_I": 2,
    "Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|not_specified|not_provided": 1,
    "PRX-related_disorder": 4,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F": 3,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Dejerine-Sottas_disease": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Autosomal_recessive_Dejerine-Sottas_syndrome|Charcot-Marie-Tooth_disease_type_4|Peripheral_neuropathy": 1,
    "Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_specified": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4|not_provided|PRX-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4|Distal_spinal_muscular_atrophy": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "PRX-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "PRX-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4F|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_4F|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|_type_I|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4F": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4F|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F": 1,
    "PRX-related_disorder|not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|PRX-related_disorder|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_specified|not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Dejerine-Sottas_disease|Autosomal_recessive_Dejerine-Sottas_syndrome|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_4|not_specified|Charcot-Marie-Tooth_disease_type_4F": 1,
    "Charcot-Marie-Tooth_disease_type_4F|PRX-related_disorder|Charcot-Marie-Tooth_disease_type_4|Gaucher_disease": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_type_4|Charcot-Marie-Tooth_disease_type_4F|Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4F|Dejerine-Sottas_disease|Charcot-Marie-Tooth_disease_type_4|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4F|PRX-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4F|not_specified": 1,
    "SPTBN4-related_disorder|not_specified": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|Inborn_genetic_diseases": 11,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|not_provided": 8,
    "SPTBN4-related_disorder|not_provided": 10,
    "SPTBN4-related_disorder": 21,
    "not_provided|SPTBN4-related_disorder": 13,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness": 30,
    "Inborn_genetic_diseases|not_provided|SPTBN4-related_disorder": 2,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|SPTBN4-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness": 3,
    "Inborn_genetic_diseases|SPTBN4-related_disorder": 2,
    "not_provided|Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|not_provided|SPTBN4-related_disorder": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|not_specified": 1,
    "SPTBN4-related_neurodevelopmental_disorder": 2,
    "Hypotonia|Delayed_myelination|Global_developmental_delay": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Neurodevelopmental_disorder_with_hypotonia|_neuropathy|_and_deafness": 1,
    "SPTBN4-related_disorder|not_provided|not_specified": 1,
    "LTBP4-related_disorder": 17,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 51,
    "not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 28,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_provided": 13,
    "not_provided|LTBP4-related_disorder": 7,
    "LTBP4-related_disorder|not_provided": 8,
    "LTBP4-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 7,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|Inborn_genetic_diseases": 3,
    "LTBP4-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 3,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|Inborn_genetic_diseases|not_provided": 2,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_specified|not_provided": 3,
    "not_provided|not_specified|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 6,
    "not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_specified|LTBP4-related_disorder": 1,
    "LTBP4-related_disorder|Inborn_genetic_diseases|not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 1,
    "not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|LTBP4-related_disorder": 1,
    "Inborn_genetic_diseases|LTBP4-related_disorder|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 1,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_provided|LTBP4-related_disorder|not_specified": 1,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_provided|not_specified": 4,
    "Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 1,
    "not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_specified": 3,
    "LTBP4-related_disorder|not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies|not_specified": 1,
    "not_specified|not_provided|LTBP4-related_disorder": 1,
    "not_provided|LTBP4-related_disorder|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 1,
    "Cutis_Laxa_Syndrome": 1,
    "LTBP4-related_disorder|not_provided|not_specified|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 1,
    "LTBP4-related_disorder|not_provided|Cutis_laxa_with_severe_pulmonary|_gastrointestinal_and_urinary_anomalies": 1,
    "not_provided|LTBP4-related_disorder|not_specified": 1,
    "LTBP4-related_disorder|not_specified|not_provided": 2,
    "Nephrotic_syndrome|_type_9|not_specified": 1,
    "Kidney_disorder|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_9|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Nephrotic_syndrome|_type_9": 4,
    "Mitochondrial_disease|not_provided|Nephrotic_syndrome|_type_9": 1,
    "Nephrotic_syndrome|_type_9": 21,
    "COQ8B-related_disorder|not_provided": 4,
    "Nephrotic_syndrome|_type_9|not_provided|See_cases": 1,
    "Nephrotic_syndrome|_type_9|not_provided": 8,
    "not_provided|COQ8B-related_disorder": 3,
    "not_provided|not_specified|Nephrotic_syndrome|_type_9": 1,
    "Kidney_disorder|not_specified|not_provided": 1,
    "COQ8B-related_disorder": 1,
    "not_provided|COQ8B-related_disorder|not_specified": 3,
    "not_provided|COQ8B-related_disorder|Nephrotic_syndrome|_type_9": 1,
    "Nephrotic_syndrome|_type_9|not_specified|not_provided": 2,
    "COQ8B-related_disorder|Nephrotic_syndrome|_type_9": 1,
    "Nephrotic_syndrome|Nephrotic_syndrome|_type_9": 1,
    "not_specified|COQ8B-related_disorder": 1,
    "COQ8B-related_disorder|not_specified|not_provided": 1,
    "Nephrotic_syndrome|_type_9|Focal_segmental_glomerulosclerosis": 1,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_type_9|not_provided": 1,
    "Retinitis_pigmentosa|COQ8B-related_disorder|not_provided": 1,
    "ITPKC-related_disorder": 9,
    "ITPKC-related_disorder|Reclassified_-_variant_of_unknown_significance": 1,
    "Spliceosomepathy": 3,
    "SNRPA-related_disorder": 5,
    "SNRPA-related_disorder|not_provided": 1,
    "MIA-related_disorder": 3,
    "EGLN2-related_disorder": 1,
    "Tegafur_response": 1,
    "Nicotine|_poor_metabolism_of|Warfarin_response": 1,
    "CYP2B6-related_disorder": 12,
    "Efavirenz_response": 7,
    "CYP2B6-related_disorder|not_provided": 1,
    "CYP2B6-related_disorder|Efavirenz_response|nevirapine_response_-_Metabolism/PK|efavirenz_response_-_Metabolism/PK|efavirenz_response_-_Toxicity": 1,
    "CYP2B6-related_disorder|not_provided|Efavirenz_response": 1,
    "nevirapine_response_-_Toxicity|CYP2B6-related_disorder": 1,
    "AXL-related_disorder": 9,
    "not_provided|AXL-related_disorder": 6,
    "AXL-related_disorder|not_provided|not_specified": 1,
    "AXL-related_disorder|not_provided": 5,
    "not_provided|not_specified|AXL-related_disorder": 1,
    "not_provided|Amenorrhea|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia": 1,
    "Encephalopathy|IL10-related_early-onset_inflammatory_bowel_disease|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy": 2,
    "TGFB1-related_disorder": 2,
    "not_provided|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy": 1,
    "TGFB1-related_disorder|not_provided|not_specified": 1,
    "TGFB1-related_disorder|not_provided": 2,
    "Diaphyseal_dysplasia|Cystic_fibrosis|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|not_specified|not_provided": 1,
    "not_provided|Diaphyseal_dysplasia|Cystic_fibrosis|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|Inborn_genetic_diseases|TGFB1-related_disorder": 1,
    "Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|not_provided": 2,
    "Diaphyseal_dysplasia": 7,
    "not_provided|Diaphyseal_dysplasia": 2,
    "Inborn_genetic_diseases|not_provided|Diaphyseal_dysplasia": 1,
    "not_provided|Diaphyseal_dysplasia|See_cases": 1,
    "not_provided|TGFB1-related_disorder": 3,
    "Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy": 1,
    "not_provided|Diaphyseal_dysplasia|Cystic_fibrosis|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy": 1,
    "not_provided|Cystic_fibrosis|Diaphyseal_dysplasia|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy": 1,
    "Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|Encephalopathy|IL10-related_early-onset_inflammatory_bowel_disease": 1,
    "Diaphyseal_dysplasia|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|Cystic_fibrosis|Inborn_genetic_diseases|not_provided": 1,
    "Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|not_specified|not_provided|Meckel_syndrome|_type_10|Breast_cancer|_invasive|_susceptibility_to|Diaphyseal_dysplasia|Cystic_fibrosis": 1,
    "Diaphyseal_dysplasia|Inflammatory_bowel_disease|_immunodeficiency|_and_encephalopathy|Cystic_fibrosis|not_provided": 1,
    "not_specified|not_provided|Meckel_syndrome|_type_10|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "B9D2-related_disorder": 1,
    "not_specified|Meckel_syndrome|_type_10|not_provided": 1,
    "Meckel_syndrome|_type_10": 3,
    "Meckel-Gruber_syndrome|Joubert_syndrome|Meckel_syndrome|_type_10|not_specified|not_provided": 1,
    "Joubert_syndrome_34|Joubert_syndrome_and_related_disorders|Joubert_syndrome": 1,
    "B9D2-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_10": 1,
    "Joubert_syndrome_and_related_disorders|Meckel_syndrome|_type_10": 1,
    "B9D2-related_disorder|Joubert_syndrome|Meckel-Gruber_syndrome|Ciliopathy": 1,
    "Joubert_syndrome_34|Joubert_syndrome|Joubert_syndrome_and_related_disorders": 1,
    "not_provided|Meckel_syndrome|_type_10": 3,
    "Joubert_syndrome|Meckel-Gruber_syndrome|B9D2-related_disorder": 1,
    "Ciliopathy|not_provided|Joubert_syndrome|Meckel-Gruber_syndrome": 1,
    "Joubert_syndrome_34|Joubert_syndrome": 1,
    "Joubert_syndrome|Meckel-Gruber_syndrome|Meckel_syndrome|_type_10|not_specified|not_provided": 2,
    "Cerebellar_ataxia|_brain_abnormalities|_and_cardiac_conduction_defects": 8,
    "Cerebellar_ataxia|_brain_abnormalities|_and_cardiac_conduction_defects|not_provided": 1,
    "BCKDHA-related_disorder|not_provided|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_1A|Inborn_genetic_diseases|not_provided|Maple_syrup_urine_disease|not_specified": 1,
    "Maple_syrup_urine_disease|not_specified|Inborn_genetic_diseases": 1,
    "BCKDHA-related_disorder|Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_provided": 1,
    "not_provided|Maple_syrup_urine_disease|Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A": 1,
    "Inborn_genetic_diseases|not_provided|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|not_specified|BCKDHA-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1A|not_provided|Maple_syrup_urine_disease|not_specified": 1,
    "not_specified|Maple_syrup_urine_disease_type_1A|not_provided|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Maple_syrup_urine_disease": 1,
    "Inborn_genetic_diseases|not_provided|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|BCKDHA-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_specified": 1,
    "not_specified|Maple_syrup_urine_disease|BCKDHA-related_disorder": 2,
    "not_provided|Maple_syrup_urine_disease|Inborn_genetic_diseases": 1,
    "BCKDHA-related_disorder|Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease|not_specified|BCKDHA-related_disorder": 1,
    "not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_specified|BCKDHA-related_disorder": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Maple_syrup_urine_disease|BCKDHA-related_disorder": 1,
    "not_specified|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|not_provided|BCKDHA-related_disorder": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|not_specified": 1,
    "BCKDHA-related_disorder|Maple_syrup_urine_disease": 4,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 3,
    "BCKDHA-related_disorder|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "not_provided|Maple_syrup_urine_disease|not_specified|Maple_syrup_urine_disease_type_1A|BCKDHA-related_disorder": 1,
    "Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|BCKDHA-related_disorder": 1,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_provided": 1,
    "Maple_syrup_urine_disease_type_1A|Inborn_genetic_diseases|Maple_syrup_urine_disease": 2,
    "BCKDHA-related_disorder|Maple_syrup_urine_disease|Inborn_genetic_diseases": 1,
    "BCKDHA-related_disorder|Inborn_genetic_diseases|not_provided|Maple_syrup_urine_disease": 2,
    "Inborn_genetic_diseases|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A": 3,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|Inborn_genetic_diseases": 3,
    "not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|Inborn_genetic_diseases": 1,
    "Maple_syrup_urine_disease|Inborn_genetic_diseases|Maple_syrup_urine_disease_type_1A": 1,
    "BCKDHA-related_disorder|not_provided|not_specified|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|BCKDHA-related_disorder": 1,
    "Maple_syrup_urine_disease_type_1A|not_specified": 1,
    "Intellectual_disability|Maple_syrup_urine_disease": 1,
    "not_specified|Maple_syrup_urine_disease|not_provided|Maple_syrup_urine_disease_type_1A": 2,
    "Inborn_genetic_diseases|BCKDHA-related_disorder|not_specified|not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 1,
    "Maple_syrup_urine_disease_type_1A|not_specified|Inborn_genetic_diseases|Maple_syrup_urine_disease|not_provided": 1,
    "not_specified|not_provided|Maple_syrup_urine_disease|BCKDHA-related_disorder": 1,
    "not_specified|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A|not_provided": 1,
    "Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Maple_syrup_urine_disease_type_1A|BCKDHA-related_disorder|Maple_syrup_urine_disease": 1,
    "Inborn_genetic_diseases|not_provided|BCKDHA-related_disorder|not_specified|Maple_syrup_urine_disease": 1,
    "Inborn_genetic_diseases|not_provided|Maple_syrup_urine_disease_type_1A|Maple_syrup_urine_disease": 3,
    "Maple_syrup_urine_disease_type_1A|not_specified|Maple_syrup_urine_disease|not_provided": 1,
    "BCKDHA-related_disorder|Maple_syrup_urine_disease|Maple_syrup_urine_disease_type_1A": 1,
    "Diamond-Blackfan_anemia_1": 44,
    "not_provided|Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia": 5,
    "not_specified|Diamond-Blackfan_anemia_1": 2,
    "Diamond-Blackfan_anemia|RPS19-related_disorder": 3,
    "not_provided|Diamond-Blackfan_anemia|RPS19-related_disorder|Diamond-Blackfan_anemia_1|not_specified": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_1": 14,
    "not_specified|Diamond-Blackfan_anemia|not_provided|Diamond-Blackfan_anemia_1": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_1|not_provided": 1,
    "Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_1|not_specified": 1,
    "Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia": 13,
    "not_provided|Diamond-Blackfan_anemia|Diamond-Blackfan_anemia_1": 1,
    "Diamond-Blackfan_anemia|Hepatoblastoma|not_provided|Diamond-Blackfan_anemia_1": 1,
    "RPS19-related_disorder|not_provided|Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia": 1,
    "Diamond-Blackfan_anemia|not_provided|RPS19-related_disorder": 1,
    "Landsteiner-Wiener_phenotype|Diamond-Blackfan_anemia": 1,
    "RPS19-related_disorder": 1,
    "not_provided|Diamond-Blackfan_anemia_1": 1,
    "not_specified|not_provided|Diamond-Blackfan_anemia_1|Diamond-Blackfan_anemia": 2,
    "Diamond-Blackfan_anemia|not_specified|not_provided": 1,
    "Agammaglobulinemia_3|_autosomal_recessive": 125,
    "Agammaglobulinemia_3|_autosomal_recessive|not_specified": 8,
    "not_provided|CD79A-related_disorder": 2,
    "not_specified|Agammaglobulinemia_3|_autosomal_recessive": 6,
    "not_provided|Agammaglobulinemia_3|_autosomal_recessive": 3,
    "Agammaglobulinemia_3|_autosomal_recessive|not_provided": 3,
    "Agammaglobulinemia_3|_autosomal_recessive|not_provided|not_specified": 1,
    "Agammaglobulinemia_3|_autosomal_recessive|not_specified|not_provided": 1,
    "not_specified|Agammaglobulinemia_3|_autosomal_recessive|Autosomal_recessive_agammaglobulinemia_1": 1,
    "CD79A-related_disorder|Agammaglobulinemia_3|_autosomal_recessive": 1,
    "Agammaglobulinemia_3|_autosomal_recessive|CD79A-related_disorder": 1,
    "CD79A-related_disorder": 1,
    "not_provided|Immunodeficiency_62": 1,
    "ARHGEF1-related_disorder|not_provided": 7,
    "not_provided|ARHGEF1-related_disorder": 10,
    "Immunodeficiency_62": 6,
    "not_provided|ARHGEF1-related_disorder|not_specified": 1,
    "ARHGEF1-related_disorder": 1,
    "not_specified|not_provided|Immunodeficiency_62": 1,
    "not_specified|Immunodeficiency_62|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_99": 13,
    "Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12|not_provided": 3,
    "Dystonia_12|Alternating_hemiplegia_of_childhood_2": 13,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|not_provided|Dystonia_12": 1,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12": 19,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Alternating_hemiplegia_of_childhood_2": 1,
    "Dystonia_12|not_specified|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Alternating_hemiplegia_of_childhood_2": 1,
    "Dystonia_12": 705,
    "Dystonia_12|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2": 1,
    "Dystonia_12|not_provided": 51,
    "ATP1A3-related_disorder|Alternating_hemiplegia_of_childhood_2|Dystonia_12|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99": 1,
    "not_provided|Dystonia_12|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Dystonia_12|not_provided": 1,
    "ATP1A3-related_disorder|Dystonia_12": 11,
    "Alternating_hemiplegia_of_childhood_2": 18,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|not_provided": 2,
    "Dystonia_12|ATP1A3-related_disorder": 8,
    "not_specified|Dystonia_12|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2": 1,
    "not_specified|Dystonia_12|not_provided": 1,
    "not_provided|ATP1A3-related_disorder|Dystonia_12": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 10,
    "not_provided|Alternating_hemiplegia_of_childhood_2": 3,
    "Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "ATP1A3-related_disorder|Hemiplegia|Epilepsy|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 2,
    "Developmental_and_epileptic_encephalopathy_99|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 2,
    "Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Developmental_and_epileptic_encephalopathy_99": 3,
    "Dystonia_12|Inborn_genetic_diseases": 5,
    "Dystonia_12|not_provided|Alternating_hemiplegia_of_childhood_2": 1,
    "ATP1A3-associated_neurological_disorder|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Seizure": 1,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99": 1,
    "not_provided|ATP1A3-related_disorder": 1,
    "Dystonia_12|not_specified": 9,
    "not_specified|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "Dystonia_12|not_provided|ATP1A3-related_disorder": 1,
    "ATP1A3-related_disorder|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Developmental_and_epileptic_encephalopathy_99|Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_2": 1,
    "not_specified|Dystonia_12": 7,
    "ATP1A3-related_disorder": 8,
    "Inborn_genetic_diseases|Dystonia_12": 5,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 2,
    "not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 2,
    "ATP1A3-associated_neurological_disorder": 3,
    "Dystonia_12|not_provided|ATP1A3-related_disorder|Inborn_genetic_diseases": 1,
    "Dystonia_12|not_provided|not_specified": 2,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_specified|Alternating_hemiplegia_of_childhood_2|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|not_provided|ATP1A3-related_disorder": 1,
    "Inborn_genetic_diseases|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "Dystonic_disorder|Seizure|Dyskinesia|Neurodevelopmental_delay|Developmental_and_epileptic_encephalopathy_99|Inborn_genetic_diseases|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_specified|not_provided|Oculogyric_crisis|Hemiplegia|Global_developmental_delay": 1,
    "ATP1A3-related_disorder|not_provided|Dystonia_12|Alternating_hemiplegia_of_childhood_2": 1,
    "Neurodevelopmental_delay|Dystonia_12|not_provided|Alternating_hemiplegia_of_childhood_2": 1,
    "not_provided|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|ATP1A3-related_disorder": 1,
    "Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2": 1,
    "Alternating_hemiplegia_of_childhood_2|not_provided": 1,
    "ATP1A3-related_disorder|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|Dystonic_disorder|Oculogyric_crisis|Tetraparesis|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "not_specified|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "ATP1A3-associated_neurological_disorder|Alternating_hemiplegia_of_childhood": 1,
    "Developmental_and_epileptic_encephalopathy_99|Inborn_genetic_diseases|not_provided|Dystonia_12": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|not_specified|ATP1A3-related_disorder|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12": 1,
    "not_provided|Dystonia_12|Alternating_hemiplegia_of_childhood_2": 2,
    "ATP1A3-associated_neurological_disorder|Inborn_genetic_diseases|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "Alternating_hemiplegia_of_childhood_2|Inborn_genetic_diseases|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Seizure|ATP1A3-related_disorder|not_provided|ATP1A3-associated_neurological_disorder": 1,
    "not_provided|not_specified|Dystonia_12": 3,
    "Dystonia_12|Inborn_genetic_diseases|not_provided": 1,
    "ATP1A3-related_disorder|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Dystonia_12|Developmental_and_epileptic_encephalopathy_99": 1,
    "not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99": 1,
    "Developmental_and_epileptic_encephalopathy_99|not_provided|Dystonia_12": 1,
    "Inborn_genetic_diseases|Dystonia_12|Seizure": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "ATP1A3-related_disorder|Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|not_provided|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2": 1,
    "Dystonia_12|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "not_provided|Dystonia_12|Inborn_genetic_diseases": 1,
    "ATP1A3-related_disorder|Dystonia_12|Alternating_hemiplegia_of_childhood_2": 1,
    "Inborn_genetic_diseases|not_provided|Dystonia_12": 2,
    "Dystonia_12|Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "Dystonia_12|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Dystonia_12|Developmental_and_epileptic_encephalopathy_99": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 2,
    "ATP1A3-related_disorder|Dystonia_12|not_provided": 2,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12|not_provided|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "Dystonia_12|Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_2": 1,
    "Developmental_and_epileptic_encephalopathy_99|Dystonia_12|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "ATP1A3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|not_specified": 1,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided": 1,
    "Dystonia_12|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Alternating_hemiplegia_of_childhood_2|Dystonia_12|ATP1A3-related_disorder": 1,
    "Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99": 3,
    "Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|ATP1A3-related_disorder": 1,
    "not_specified|not_provided|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "Dystonia_12|not_provided|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 2,
    "Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2|Dystonia_12|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Inborn_genetic_diseases|not_provided": 1,
    "Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_2|Inborn_genetic_diseases|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Dystonia_12|Developmental_and_epileptic_encephalopathy_99": 1,
    "Developmental_and_epileptic_encephalopathy_99|not_provided|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12": 1,
    "Inborn_genetic_diseases|Dystonia_12|not_provided": 1,
    "Seizures|_benign_familial_neonatal|_1": 76,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99": 1,
    "Alternating_hemiplegia_of_childhood_2|not_specified|Inborn_genetic_diseases|Dystonia_12|not_provided": 1,
    "Alternating_hemiplegia_of_childhood": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "not_provided|ATP1A3-related_disorder|not_specified|Dystonia_12": 1,
    "not_provided|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Inborn_genetic_diseases": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Dystonia_12": 1,
    "Dystonia_12|Delayed_speech_and_language_development|Apnea|Seizure|Oculogyric_crisis|Hemiplegia": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_99": 1,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy_99|not_provided|not_specified|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "Developmental_and_epileptic_encephalopathy_99|Dystonia_12|not_specified|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "not_specified|Dystonia_12|Inborn_genetic_diseases": 1,
    "Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|Alternating_hemiplegia_of_childhood_2": 1,
    "Alternating_hemiplegia_of_childhood_2|not_specified|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Dystonia_12": 1,
    "ATP1A3-related_disorder|not_provided|Dystonia_12": 1,
    "Intellectual_disability|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome": 1,
    "ATP1A3-associated_neurological_disorder|Dystonia_12|not_provided": 1,
    "Dystonia_12|Alternating_hemiplegia_of_childhood_2|not_provided|Epicanthus|Ventriculomegaly|Abnormal_earlobe_morphology|Depressed_nasal_bridge|Seizure": 1,
    "not_provided|ATP1A3-related_disorder|Alternating_hemiplegia_of_childhood_2|Dystonia_12|Juvenile_onset_psychosis": 1,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder|not_provided|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_99|not_provided|Dystonia_12|ATP1A3-related_disorder|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "not_provided|Hereditary_ataxia|Dystonia_12": 1,
    "Dystonia_12|Developmental_and_epileptic_encephalopathy_99|not_provided|Alternating_hemiplegia_of_childhood_2|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy_99|not_provided|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Dystonia_12|Alternating_hemiplegia_of_childhood_2|ATP1A3-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder|Dystonia_12|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy_99|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_specified|not_provided|Alternating_hemiplegia_of_childhood_2|Dystonia_12": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy_99|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2": 1,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12|Inborn_genetic_diseases|not_provided": 1,
    "Dystonia_12|ATP1A3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99|ATP1A3-related_disorder|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|not_provided|Dystonia_12": 1,
    "Alternating_hemiplegia_of_childhood|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Alternating_hemiplegia_of_childhood_2|Developmental_and_epileptic_encephalopathy_99": 1,
    "Alternating_hemiplegia_of_childhood_2|Dystonia_12|Cerebellar_ataxia-areflexia-pes_cavus-optic_atrophy-sensorineural_hearing_loss_syndrome|Developmental_and_epileptic_encephalopathy_99": 1,
    "Alternating_hemiplegia_of_childhood|Dystonia_12": 1,
    "GRIK5-related_disorder": 16,
    "GRIK5-related_disorder|not_provided": 1,
    "not_provided|GRIK5-related_disorder": 1,
    "not_specified|ZNF526-related_disorder|not_provided": 1,
    "not_provided|Dentici-Novelli_neurodevelopmental_syndrome|Pulmonic_stenosis|Noonan-like_facies|Intellectual_disability": 1,
    "ZNF526-related_disorder|not_provided|not_specified": 2,
    "not_provided|not_specified|ZNF526-related_disorder": 1,
    "Dentici-Novelli_neurodevelopmental_syndrome": 4,
    "not_specified|Dentici-Novelli_neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|ZNF526-related_disorder": 1,
    "ZNF526-related_disorder": 4,
    "Inborn_genetic_diseases|ZNF526-related_disorder": 1,
    "ERF-related_disorder|TWIST1-related_craniosynostosis": 3,
    "ERF-related_disorder": 8,
    "Noonan_Syndrome-like_developmental_disorder": 3,
    "TWIST1-related_craniosynostosis|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|TWIST1-related_craniosynostosis": 1,
    "Craniosynostosis_4": 12,
    "Chitayat_syndrome|Craniosynostosis_4|Inborn_genetic_diseases|TWIST1-related_craniosynostosis": 1,
    "ERF-related_disorder|Neurodevelopmental_disorder|Noonan-like_syndrome|Chitayat_syndrome|Craniosynostosis_4|not_provided|TWIST1-related_craniosynostosis|Noonan_Syndrome-like_developmental_disorder": 1,
    "TWIST1-related_craniosynostosis|not_provided": 3,
    "Chitayat_syndrome|Craniosynostosis_4": 2,
    "Chitayat_syndrome|Craniosynostosis_4|Inborn_genetic_diseases|Noonan-like_syndrome|not_provided|TWIST1-related_craniosynostosis|See_cases": 1,
    "TWIST1-related_craniosynostosis|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Craniosynostosis_4|Noonan_Syndrome-like_developmental_disorder": 1,
    "TWIST1-related_craniosynostosis|ERF-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|TWIST1-related_craniosynostosis|Noonan_Syndrome-like_developmental_disorder": 1,
    "TWIST1-related_craniosynostosis|Noonan_Syndrome-like_developmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Craniosynostosis_4|TWIST1-related_craniosynostosis": 1,
    "Chitayat_syndrome|Craniosynostosis_4|Noonan-like_syndrome|not_provided|TWIST1-related_craniosynostosis": 1,
    "not_provided|Inborn_genetic_diseases|Chitayat_syndrome|Craniosynostosis_4": 1,
    "TWIST1-related_craniosynostosis|Chitayat_syndrome|Craniosynostosis_4": 1,
    "Inborn_genetic_diseases|Craniosynostosis_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Chitayat_syndrome": 1,
    "Inborn_genetic_diseases|ERF-related_disorder|Craniosynostosis_4|not_provided|TWIST1-related_craniosynostosis": 1,
    "Inborn_genetic_diseases|Craniosynostosis_4|See_cases|TWIST1-related_craniosynostosis": 1,
    "Craniosynostosis_4|not_specified|not_provided": 1,
    "Multiple_myeloma|not_provided": 1,
    "Craniosynostosis_4|not_provided|TWIST1-related_craniosynostosis": 1,
    "Noonan-like_syndrome|See_cases": 1,
    "Common_craniosynostosis_syndromes": 1,
    "Craniosynostosis_4|ERF-related_disorder": 1,
    "not_specified|Craniosynostosis_4": 1,
    "not_provided|Craniosynostosis_4": 1,
    "not_provided|CIC-related_disorder": 17,
    "not_specified|CIC-related_disorder|not_provided": 2,
    "Intellectual_disability|_autosomal_dominant_45": 103,
    "CIC-related_disorder": 60,
    "not_specified|CIC-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_45|CIC-related_disorder": 2,
    "not_provided|Intellectual_disability|_autosomal_dominant_45": 3,
    "CIC-related_disorder|not_specified|not_provided": 2,
    "See_cases|CIC-related_disorder|Intellectual_disability|_autosomal_dominant_45|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_45|not_specified|not_provided": 1,
    "CIC-related_disorder|not_provided": 11,
    "not_specified|Intellectual_disability|_autosomal_dominant_45": 1,
    "CIC-related_disorder|Intellectual_disability|_autosomal_dominant_45": 2,
    "CIC-related_disorder|not_specified": 2,
    "Intellectual_disability|_autosomal_dominant_45|Inborn_genetic_diseases": 8,
    "CIC-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "CIC-related_neurodevelopmental_disorders|Intellectual_disability|_autosomal_dominant_45|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_45|not_provided": 9,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_45": 1,
    "Intellectual_disability|_autosomal_dominant_45|CIC-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_45": 3,
    "Inborn_genetic_diseases|CIC-related_disorder": 1,
    "Inborn_genetic_diseases|CIC-related_disorder|not_provided": 1,
    "CIC-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "CIC-related_neurodevelopmental_disorders": 1,
    "CIC-related_disorder|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_dominant_45|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_45|not_provided": 2,
    "See_cases|not_specified|CIC-related_disorder": 1,
    "Marfanoid_habitus_and_intellectual_disability|Intellectual_disability|_autosomal_dominant_45": 1,
    "CIC-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_autosomal_dominant_45|Intellectual_disability|_autosomal_dominant_1": 1,
    "CIC-related_disorder|not_specified|not_provided|Intellectual_disability": 1,
    "not_provided|CIC-related_disorder|Intellectual_disability|_autosomal_dominant_45": 1,
    "Intellectual_disability|_autosomal_dominant_45|See_cases|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CIC-related_disorder|Intellectual_disability": 1,
    "NK-cell_enteropathy|not_specified|Intellectual_disability|_autosomal_dominant_45": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_45|not_provided": 1,
    "MEGF8-related_Carpenter_syndrome": 400,
    "Inborn_genetic_diseases|MEGF8-related_Carpenter_syndrome": 29,
    "Inborn_genetic_diseases|MEGF8-related_disorder|MEGF8-related_Carpenter_syndrome|not_provided": 1,
    "MEGF8-related_disorder": 16,
    "MEGF8-related_Carpenter_syndrome|not_provided": 31,
    "Inborn_genetic_diseases|not_provided|MEGF8-related_Carpenter_syndrome": 6,
    "MEGF8-related_Carpenter_syndrome|Inborn_genetic_diseases": 36,
    "Inborn_genetic_diseases|not_specified|MEGF8-related_Carpenter_syndrome": 1,
    "not_specified|not_provided|MEGF8-related_Carpenter_syndrome": 2,
    "not_provided|MEGF8-related_Carpenter_syndrome": 51,
    "not_provided|MEGF8-related_Carpenter_syndrome|Inborn_genetic_diseases": 6,
    "MEGF8-related_disorder|Inborn_genetic_diseases|MEGF8-related_Carpenter_syndrome": 2,
    "MEGF8-related_Carpenter_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "not_specified|MEGF8-related_Carpenter_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|MEGF8-related_Carpenter_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|MEGF8-related_Carpenter_syndrome": 1,
    "not_provided|MEGF8-related_disorder": 3,
    "MEGF8-related_Carpenter_syndrome|Inborn_genetic_diseases|not_provided": 4,
    "MEGF8-related_disorder|MEGF8-related_Carpenter_syndrome": 3,
    "MEGF8-related_disorder|not_provided": 1,
    "MEGF8-related_Carpenter_syndrome|MEGF8-related_disorder": 9,
    "MEGF8-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MEGF8-related_Carpenter_syndrome|MEGF8-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|MEGF8-related_Carpenter_syndrome": 1,
    "MEGF8-related_Carpenter_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|MEGF8-related_disorder|MEGF8-related_Carpenter_syndrome": 1,
    "MEGF8-related_disorder|not_provided|MEGF8-related_Carpenter_syndrome": 1,
    "MEGF8-related_Carpenter_syndrome|MEGF8-related_disorder|not_provided": 2,
    "MEGF8-related_disorder|Inborn_genetic_diseases|not_provided|MEGF8-related_Carpenter_syndrome": 1,
    "MEGF8-related_Carpenter_syndrome|not_provided|MEGF8-related_disorder": 2,
    "Inborn_genetic_diseases|MEGF8-related_disorder|not_provided|MEGF8-related_Carpenter_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|MEGF8-related_Carpenter_syndrome": 1,
    "Craniosynostosis_syndrome|Polydactyly|MEGF8-related_Carpenter_syndrome": 1,
    "LIPE-related_familial_partial_lipodystrophy": 5,
    "LIPE-related_disorder|LIPE-related_familial_partial_lipodystrophy": 2,
    "not_provided|LIPE-related_disorder": 7,
    "not_provided|LIPE-related_familial_partial_lipodystrophy": 1,
    "LIPE-related_disorder": 7,
    "LIPE-related_familial_partial_lipodystrophy|Inborn_genetic_diseases": 1,
    "LIPE-related_disorder|not_provided|LIPE-related_familial_partial_lipodystrophy": 1,
    "not_specified|LIPE-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|LIPE-related_disorder": 1,
    "not_specified|not_provided|LIPE-related_disorder": 2,
    "not_specified|LIPE-related_disorder": 1,
    "See_cases|LIPE-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|LIPE-related_disorder": 1,
    "LIPE-related_disorder|not_provided|not_specified": 1,
    "LIPE-related_disorder|not_provided": 1,
    "LIPE-related_familial_partial_lipodystrophy|not_provided": 1,
    "Ethylmalonic_encephalopathy": 351,
    "Ethylmalonic_encephalopathy|not_provided": 11,
    "Ethylmalonic_encephalopathy|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Ethylmalonic_encephalopathy": 5,
    "not_provided|Ethylmalonic_encephalopathy": 15,
    "not_specified|Ethylmalonic_encephalopathy": 3,
    "Ethylmalonic_encephalopathy|ETHE1-related_disorder|not_specified": 1,
    "ETHE1-related_disorder": 1,
    "Abnormality_of_the_nervous_system|Ethylmalonic_encephalopathy": 1,
    "Ethylmalonic_encephalopathy|not_specified": 3,
    "Ethylmalonic_encephalopathy|Inborn_genetic_diseases|not_specified": 1,
    "Ethylmalonic_encephalopathy|Inborn_genetic_diseases|not_provided": 2,
    "ETHE1-related_disorder|not_provided|Ethylmalonic_encephalopathy": 1,
    "not_provided|not_specified|Ethylmalonic_encephalopathy": 1,
    "ETHE1-related_disorder|Inborn_genetic_diseases|not_specified|Ethylmalonic_encephalopathy": 1,
    "not_provided|ETHE1-related_disorder|Ethylmalonic_encephalopathy": 1,
    "Ethylmalonic_encephalopathy|not_provided|not_specified": 1,
    "Ethylmalonic_encephalopathy|ETHE1-related_disorder": 1,
    "not_specified|Ethylmalonic_encephalopathy|not_provided": 1,
    "not_specified|not_provided|Ethylmalonic_encephalopathy": 1,
    "Laryngeal_squamous_cell_carcinoma": 4,
    "not_provided|Spinocerebellar_ataxia|_autosomal_recessive_26": 3,
    "Spinocerebellar_ataxia|_autosomal_recessive_26": 7,
    "XRCC1-related_disorder": 4,
    "Spinocerebellar_ataxia|_autosomal_recessive_26|not_provided": 1,
    "Platinum_compounds_response_-_Efficacy|not_provided|Spinocerebellar_ataxia|_autosomal_recessive_26": 1,
    "XRCC1-related_disorder|not_provided": 2,
    "XRCC1-related_disorder|not_provided|not_specified": 1,
    "not_provided|XRCC1-related_disorder": 2,
    "not_specified|Spinocerebellar_ataxia|_autosomal_recessive_26": 1,
    "PLAUR-related_disorder": 1,
    "Heart_and_brain_malformation_syndrome": 4,
    "SMG9-related_disorder": 9,
    "Neurodevelopmental_disorder_with_intention_tremor|_pyramidal_signs|_dyspraxia|_and_ocular_anomalies": 4,
    "Heart_and_brain_malformation_syndrome|Neurodevelopmental_abnormality": 1,
    "not_provided|Heart_and_brain_malformation_syndrome": 2,
    "Heart_and_brain_malformation_syndrome|not_provided": 1,
    "Heart_and_brain_malformation_syndrome|not_provided|Abnormal_facial_shape|Abnormal_cardiovascular_system_morphology|Global_developmental_delay|Brainstem_dysplasia": 1,
    "Brainstem_dysplasia|Abnormal_facial_shape|Abnormal_cardiovascular_system_morphology|Global_developmental_delay|Heart_and_brain_malformation_syndrome": 1,
    "Dehydrated_hereditary_stomatocytosis_2": 30,
    "KCNN4-related_disorder|Dehydrated_hereditary_stomatocytosis_2": 2,
    "not_provided|Inborn_genetic_diseases|Dehydrated_hereditary_stomatocytosis_2": 1,
    "KCNN4-related_disorder": 7,
    "Dehydrated_hereditary_stomatocytosis_2|Inborn_genetic_diseases|not_provided": 1,
    "Dehydrated_hereditary_stomatocytosis_2|Inborn_genetic_diseases": 5,
    "KCNN4-related_disorder|Primary_ciliary_dyskinesia_5|Dehydrated_hereditary_stomatocytosis_2|not_provided": 1,
    "Inborn_genetic_diseases|Dehydrated_hereditary_stomatocytosis_2": 4,
    "KCNN4-related_disorder|Dehydrated_hereditary_stomatocytosis_2|Inborn_genetic_diseases": 1,
    "KCNN4-related_disorder|Dehydrated_hereditary_stomatocytosis_2|not_provided": 1,
    "not_provided|KCNN4-related_disorder": 2,
    "KCNN4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Dehydrated_hereditary_stomatocytosis_2|Inborn_genetic_diseases": 1,
    "not_provided|Dehydrated_hereditary_stomatocytosis_2": 1,
    "PVR-related_disorder": 10,
    "PVR-related_disorder|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4B": 5,
    "Hearing_loss|_autosomal_recessive_113": 2,
    "not_provided|CEACAM16-related_disorder": 4,
    "Hearing_loss|_autosomal_recessive_113|Autosomal_dominant_nonsyndromic_hearing_loss_4B|not_provided": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4B": 1,
    "not_provided|not_specified|Hearing_loss|_autosomal_recessive_113|Autosomal_dominant_nonsyndromic_hearing_loss_4B": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4B": 1,
    "CEACAM16-related_disorder|not_provided": 3,
    "CEACAM16-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "CEACAM16-related_disorder|not_provided|not_specified": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4B|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4B|not_provided|CEACAM16-related_disorder": 1,
    "Inborn_genetic_diseases|CEACAM16-related_disorder|not_specified|not_provided": 1,
    "not_provided|Hearing_loss|_autosomal_recessive_113|Nonsyndromic_genetic_hearing_loss": 1,
    "CEACAM16-related_disorder|not_specified|not_provided": 1,
    "CEACAM16-related_disorder": 1,
    "Inborn_genetic_diseases|Hearing_loss|_autosomal_recessive_113": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4B|not_provided": 1,
    "Hearing_impairment|not_provided|Hearing_loss|_autosomal_recessive_113|Autosomal_dominant_nonsyndromic_hearing_loss_4B": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4B|Hearing_loss|_autosomal_recessive_113": 1,
    "BCAM-related_disorder": 11,
    "LUTHERAN_BLOOD_GROUP_POLYMORPHISM_Lu(a)/Lu(b)|not_provided": 1,
    "BLOOD_GROUP--LUTHERAN_NULL": 3,
    "BLOOD_GROUP--LUTHERAN_SYSTEM": 1,
    "not_provided|BCAM-related_disorder": 2,
    "AUBERGER_BLOOD_GROUP_POLYMORPHISM_Au(a)/Au(b)|not_provided|BCAM-related_disorder|LuLu_phenotype|BLOOD_GROUP--LUTHERAN_SYSTEM": 1,
    "NECTIN2-related_disorder": 24,
    "NECTIN2-related_disorder|not_provided": 2,
    "not_provided|NECTIN2-related_disorder": 1,
    "Coronary_artery_disease|_severe|_susceptibility_to": 1,
    "APOE-related_disorder": 5,
    "Familial_type_3_hyperlipoproteinemia|Alzheimer_disease_2|APOE-related_disorder": 1,
    "Lipoprotein_glomerulopathy|Familial_type_3_hyperlipoproteinemia|Cardiovascular_phenotype": 1,
    "Alzheimer_disease_2": 5,
    "HYPERLIPOPROTEINEMIA|_TYPE_III|_AND_ATHEROSCLEROSIS_ASSOCIATED_WITH_APOE5": 1,
    "Alzheimer_disease_3|Alzheimer_disease_2|Alzheimer_disease_4|Sea-blue_histiocyte_syndrome|Lipoprotein_glomerulopathy|Age_related_macular_degeneration_1|Familial_type_3_hyperlipoproteinemia|Cardiovascular_phenotype|not_provided": 1,
    "APOE5_VARIANT|not_provided|Alzheimer_disease_3|Alzheimer_disease_2|Age_related_macular_degeneration_1|Sea-blue_histiocyte_syndrome|Familial_type_3_hyperlipoproteinemia|Lipoprotein_glomerulopathy": 1,
    "Cardiovascular_phenotype|Alzheimer_disease_4|Sea-blue_histiocyte_syndrome|Alzheimer_disease_2|Familial_type_3_hyperlipoproteinemia|Age_related_macular_degeneration_1|Lipoprotein_glomerulopathy|Alzheimer_disease_3": 1,
    "not_provided|Alzheimer_disease_4|Cardiovascular_phenotype": 1,
    "Familial_type_3_hyperlipoproteinemia": 7,
    "Cardiovascular_phenotype|APOE-related_disorder|not_provided": 2,
    "APOE3(-)-FREIBURG|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|APOE-related_disorder": 1,
    "Alzheimer_disease_3|Alzheimer_disease_2|Alzheimer_disease_4|Sea-blue_histiocyte_syndrome|Familial_type_3_hyperlipoproteinemia|Age_related_macular_degeneration_1|Lipoprotein_glomerulopathy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|APOE-related_disorder": 1,
    "not_provided|Familial_type_3_hyperlipoproteinemia": 1,
    "Major_depressive_disorder": 2,
    "Primary_degenerative_dementia_of_the_Alzheimer_type|_presenile_onset|not_specified|not_provided|Warfarin_response|Alzheimer_disease_2|Lipoprotein_glomerulopathy|Alzheimer_disease|Alzheimer_disease_4": 1,
    "Familial_type_3_hyperlipoproteinemia|Familial_hypercholesterolemia|Hyperlipoproteinemia": 1,
    "Alzheimer_disease_3|Alzheimer_disease_2|Alzheimer_disease_4|Age_related_macular_degeneration_1|Sea-blue_histiocyte_syndrome|Lipoprotein_glomerulopathy|Familial_type_3_hyperlipoproteinemia|Cardiovascular_phenotype|not_provided|Hypercholesterolemia": 1,
    "APOE2_VARIANT": 1,
    "Familial_type_3_hyperlipoproteinemia|Alzheimer_disease_2": 1,
    "APOE-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Familial_type_3_hyperlipoproteinemia|Alzheimer_disease_2": 1,
    "Lipoprotein_glomerulopathy|Familial_type_3_hyperlipoproteinemia": 1,
    "Lipoprotein_glomerulopathy": 3,
    "Hyperlipoproteinemia|_type_III|_due_to_APOE2": 1,
    "Cardiovascular_phenotype|APOE-related_disorder|Familial_hypercholesterolemia|not_provided|Sea-blue_histiocyte_syndrome": 1,
    "not_specified|not_provided|Warfarin_response|Familial_type_3_hyperlipoproteinemia|Hypercholesterolemia|atorvastatin_response_-_Efficacy": 1,
    "Cardiovascular_phenotype|not_provided|APOE-related_disorder": 1,
    "Sea-blue_histiocyte_syndrome|Familial_type_3_hyperlipoproteinemia|Age_related_macular_degeneration_1|Alzheimer_disease_3|Alzheimer_disease_4|Lipoprotein_glomerulopathy|Alzheimer_disease_2|Cardiovascular_phenotype|not_provided": 1,
    "Familial_type_3_hyperlipoproteinemia|not_provided|HYPERLIPOPROTEINEMIA|_TYPE_III|_ASSOCIATED_WITH_APOE3(WASHINGTON)": 1,
    "Alzheimer_disease_4|Alzheimer_disease_3|Alzheimer_disease_2|Sea-blue_histiocyte_syndrome|Familial_type_3_hyperlipoproteinemia|Age_related_macular_degeneration_1|Lipoprotein_glomerulopathy|not_provided": 1,
    "APOE2-DUNEDIN|HYPERLIPOPROTEINEMIA|_TYPE_IV/V|_DUE_TO_APOE2-DUNEDIN": 1,
    "not_provided|not_specified|Familial_type_3_hyperlipoproteinemia": 1,
    "Alzheimer_disease_2|Cardiovascular_phenotype": 2,
    "Alzheimer_disease_3|Alzheimer_disease_2|Alzheimer_disease_4|Age_related_macular_degeneration_1|Sea-blue_histiocyte_syndrome|Lipoprotein_glomerulopathy|Familial_type_3_hyperlipoproteinemia|APOE-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "APOE4_VARIANT": 1,
    "Cardiovascular_phenotype|not_provided|Familial_type_3_hyperlipoproteinemia": 1,
    "APOE-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|APOE4(+)": 1,
    "not_provided|Familial_apolipoprotein_C-II_deficiency": 3,
    "Familial_apolipoprotein_C-II_deficiency": 23,
    "Familial_apolipoprotein_C-II_deficiency|Cardiovascular_phenotype|APOC2-related_disorder|not_specified|not_provided": 1,
    "Familial_apolipoprotein_C-II_deficiency|APOLIPOPROTEIN_C-II_(PARIS)": 1,
    "Familial_apolipoprotein_C-II_deficiency|Cardiovascular_phenotype|not_provided": 2,
    "Familial_apolipoprotein_C-II_deficiency|not_provided": 5,
    "APOLIPOPROTEIN_C-II_(HAMBURG)|Familial_apolipoprotein_C-II_deficiency": 1,
    "not_provided|Familial_apolipoprotein_C-II_deficiency|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Familial_apolipoprotein_C-II_deficiency": 4,
    "Familial_apolipoprotein_C-II_deficiency|Cardiovascular_phenotype": 2,
    "APOC2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Familial_apolipoprotein_C-II_deficiency|Apolipoprotein_c-ii_variant": 1,
    "APOLIPOPROTEIN_C-II_(WAKAYAMA)|Familial_apolipoprotein_C-II_deficiency": 1,
    "not_provided|Cardiovascular_phenotype|APOC2-related_disorder": 1,
    "not_provided|Familial_apolipoprotein_C-II_deficiency|APOLIPOPROTEIN_C-II_(PADOVA)": 1,
    "APOLIPOPROTEIN_C-II_(BARI)|Familial_apolipoprotein_C-II_deficiency": 1,
    "APOLIPOPROTEIN_C-II_(SAN_FRANCISCO)|Familial_apolipoprotein_C-II_deficiency|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Familial_apolipoprotein_C-II_deficiency": 1,
    "APOLIPOPROTEIN_C-II_(AFRICAN)|Familial_apolipoprotein_C-II_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "APOLIPOPROTEIN_C-II_(AUCKLAND)|Familial_apolipoprotein_C-II_deficiency": 1,
    "APOLIPOPROTEIN_C-II_(TORONTO)|Familial_apolipoprotein_C-II_deficiency": 1,
    "APOLIPOPROTEIN_C-II_(ST._MICHAEL)|Familial_apolipoprotein_C-II_deficiency": 1,
    "APOC2-related_disorder": 1,
    "CLPTM1-related_disorder": 26,
    "not_specified|CLPTM1-related_disorder": 1,
    "CLPTM1-related_disorder|not_provided": 3,
    "not_provided|CLPTM1-related_disorder": 2,
    "CLPTM1-related_disorder|not_specified": 2,
    "not_provided|RELB-related_disorder": 7,
    "Immunodeficiency_53": 3,
    "RELB-related_disorder|not_provided": 4,
    "RELB-related_disorder": 1,
    "Immunodeficiency_53|not_provided": 3,
    "not_specified|not_provided|Immunodeficiency_53": 1,
    "TRAPPC6A-related_disorder": 9,
    "not_provided|TRAPPC6A-related_disorder": 1,
    "BLOC1S3-related_disorder": 5,
    "not_provided|BLOC1S3-related_disorder": 2,
    "Hermansky-Pudlak_syndrome_8": 6,
    "Hermansky-Pudlak_syndrome_8|Inborn_genetic_diseases": 1,
    "BLOC1S3-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_8": 1,
    "not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_8": 1,
    "not_specified|BLOC1S3-related_disorder|not_provided": 1,
    "not_specified|Hermansky-Pudlak_syndrome_8|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|BLOC1S3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "BLOC1S3-related_disorder|not_provided": 3,
    "not_specified|not_provided|BLOC1S3-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Hermansky-Pudlak_syndrome_8|not_provided": 1,
    "EXOC3L2-related_disorder|not_provided": 1,
    "Brain_malformation_renal_syndrome": 1,
    "EXOC3L2-related_brain_malformations_and/or_renal_disease": 1,
    "Brain_malformation_renal_syndrome|Meckel-Gruber_syndrome": 1,
    "Meckel-like_syndrome": 2,
    "Xeroderma_pigmentosum|_group_D": 33,
    "Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_provided": 6,
    "Xeroderma_pigmentosum|_group_D|not_provided": 13,
    "not_provided|Xeroderma_pigmentosum|_group_D": 5,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_specified|Cerebrooculofacioskeletal_syndrome_2": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases": 5,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum": 4,
    "not_specified|Xeroderma_pigmentosum|_group_D": 2,
    "Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_2": 44,
    "not_provided|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|not_specified": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|not_provided|ERCC2-related_disorder": 1,
    "Cerebrooculofacioskeletal_syndrome_2|not_provided": 20,
    "Inborn_genetic_diseases|not_provided|not_specified|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|ERCC2-related_disorder": 1,
    "Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Inborn_genetic_diseases|Xeroderma_pigmentosum|not_provided": 1,
    "not_provided|Corpus_callosum|_agenesis_of": 1,
    "Hypotrichosis_simplex|Trichothiodystrophy|ERCC2-related_disorder|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|not_provided": 1,
    "ERCC2-related_disorder|Mixed_Phenotype_Acute_Leukemia|_T/Myeloid|_Not_Otherwise_Specified|Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum": 2,
    "Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_D": 2,
    "not_specified|Trichothiodystrophy_1|_photosensitive": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_specified": 1,
    "not_provided|Xeroderma_pigmentosum|not_specified|Xeroderma_pigmentosum|_group_D": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_D|not_provided|ERCC2-related_disorder": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 5,
    "Cerebrooculofacioskeletal_syndrome_2|ERCC2-related_disorder": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum": 1,
    "not_specified|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Leukodystrophy|not_provided": 1,
    "Trichothiodystrophy_1|_photosensitive|Inborn_genetic_diseases": 1,
    "Inflammatory_bowel_disease_1|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive": 2,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2": 9,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|not_provided|Trichothiodystrophy_1|_photosensitive": 1,
    "ERCC2-related_disorder|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_provided|Xeroderma_pigmentosum": 1,
    "Cerebrooculofacioskeletal_syndrome_2|not_specified": 1,
    "not_provided|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_2|not_provided|Trichothiodystrophy_1|_photosensitive": 1,
    "ERCC2-related_disorder|Cerebrooculofacioskeletal_syndrome_2|not_provided": 1,
    "Trichothiodystrophy_1|_photosensitive|Ovarian_cancer|not_provided|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 1,
    "Trichothiodystrophy_1|_photosensitive|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|not_provided|Xeroderma_pigmentosum|_group_D": 1,
    "not_provided|Trichothiodystrophy_1|_photosensitive|Inborn_genetic_diseases": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases": 2,
    "ERCC2-related_disorder|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "ERCC2-related_disorder": 6,
    "Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_1|not_specified|Xeroderma_pigmentosum|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Ketotic_hypoglycemia|not_provided": 1,
    "Xeroderma_pigmentosum|not_provided|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D": 1,
    "not_provided|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy": 1,
    "Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_provided|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|not_provided|Cerebrooculofacioskeletal_syndrome_2|ERCC2-related_disorder|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D": 1,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_provided|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|ERCC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 1,
    "not_provided|Xeroderma_pigmentosum|Trichothiodystrophy_1|_photosensitive": 2,
    "not_provided|ERCC2-related_disorder|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases|Xeroderma_pigmentosum": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_provided|Xeroderma_pigmentosum": 1,
    "not_specified|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D": 1,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_specified|not_provided": 2,
    "ERCC2-related_disorder|Inborn_genetic_diseases|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D|not_provided": 1,
    "ERCC2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_provided": 2,
    "Trichothiodystrophy_1|_photosensitive|not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|not_specified": 1,
    "not_specified|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|not_provided": 1,
    "Xeroderma_pigmentosum|_group_D|not_provided|ERCC2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases": 1,
    "ERCC2-related_disorder|Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Leukodystrophy|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|not_provided": 2,
    "Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases|not_provided|ERCC2-related_disorder": 1,
    "Xeroderma_pigmentosum|not_provided|Inborn_genetic_diseases|ERCC2-related_disorder|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2": 1,
    "not_provided|Malignant_tumor_of_urinary_bladder|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|not_specified|Xeroderma_pigmentosum": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 1,
    "Xeroderma_pigmentosum|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 1,
    "not_provided|not_specified|Cerebrooculofacioskeletal_syndrome_2": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2": 4,
    "not_provided|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|ERCC2-related_disorder|Xeroderma_pigmentosum": 1,
    "not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D": 2,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|not_provided": 1,
    "Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Cerebrooculofacioskeletal_syndrome_2|not_provided|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 2,
    "Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|Craniopharyngioma|not_provided|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_D|not_provided": 2,
    "Cerebrooculofacioskeletal_syndrome_2|not_provided|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D": 1,
    "Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|not_provided": 1,
    "Inborn_genetic_diseases|ERCC2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_provided": 1,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|ERCC2-related_disorder|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|not_provided|not_specified|Xeroderma_pigmentosum": 1,
    "Xeroderma_pigmentosum|not_provided|ERCC2-related_disorder|Inborn_genetic_diseases": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|Inborn_genetic_diseases": 1,
    "not_specified|ERCC2-related_disorder|not_provided": 1,
    "ERCC2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Xeroderma_pigmentosum|ERCC2-related_disorder|not_provided|not_specified": 1,
    "Xeroderma_pigmentosum|Inborn_genetic_diseases|Xeroderma_pigmentosum|_group_D|not_provided": 1,
    "Xeroderma_pigmentosum|not_provided|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|_group_D|not_provided|Inborn_genetic_diseases": 3,
    "Xeroderma_pigmentosum|_group_D|not_provided|ERCC2-related_disorder": 1,
    "ERCC2-related_disorder|Xeroderma_pigmentosum|_group_D": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|not_specified|Trichothiodystrophy_1|_photosensitive": 1,
    "not_provided|Inborn_genetic_diseases|Xeroderma_pigmentosum|ERCC2-related_disorder": 1,
    "Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|not_provided": 2,
    "Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|not_provided|Xeroderma_pigmentosum": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|not_provided|Xeroderma_pigmentosum": 1,
    "Inborn_genetic_diseases|not_provided|Xeroderma_pigmentosum|_group_D": 1,
    "Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|_group_D|not_provided|not_specified": 2,
    "ERCC2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Xeroderma_pigmentosum": 1,
    "Trichothiodystrophy_1|_photosensitive|not_specified|not_provided|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Cerebrooculofacioskeletal_syndrome_2|Inborn_genetic_diseases|Ovarian_cancer|not_provided": 1,
    "ERCC2-related_disorder|not_provided|Xeroderma_pigmentosum|Xeroderma_pigmentosum|_group_D": 1,
    "Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|not_provided": 1,
    "not_provided|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Xeroderma_pigmentosum": 1,
    "not_provided|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Malignant_tumor_of_urinary_bladder|not_provided|Cerebrooculofacioskeletal_syndrome_2": 1,
    "Xeroderma_pigmentosum|Hepatoblastoma|not_specified|Xeroderma_pigmentosum|_group_D|not_provided": 1,
    "Trichothiodystrophy_1|_photosensitive|not_provided": 1,
    "not_provided|Trichothiodystrophy_1|_photosensitive|not_specified|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2": 1,
    "ERCC2-related_disorder|not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive": 1,
    "not_provided|Xeroderma_pigmentosum|Inborn_genetic_diseases": 2,
    "ERCC2-related_disorder|Cerebrooculofacioskeletal_syndrome_2|Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D": 1,
    "Trichothiodystrophy_1|_photosensitive|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|not_provided": 1,
    "Xeroderma_pigmentosum|_group_D|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|not_specified": 1,
    "not_provided|ERCC2-related_disorder|Inborn_genetic_diseases": 1,
    "Xeroderma_pigmentosum|Inborn_genetic_diseases|not_provided": 1,
    "Xeroderma_pigmentosum|not_provided|not_specified": 1,
    "not_specified|Trichothiodystrophy_1|_photosensitive|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D|not_provided|Xeroderma_pigmentosum": 1,
    "Cerebrooculofacioskeletal_syndrome_2|not_provided|Xeroderma_pigmentosum": 1,
    "not_specified|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|not_provided|Trichothiodystrophy_1|_photosensitive": 1,
    "Xeroderma_pigmentosum|_group_D|not_specified|not_provided": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|_group_D": 1,
    "Trichothiodystrophy_1|_photosensitive|Ovarian_cancer|not_specified|ERCC2-related_disorder|Xeroderma_pigmentosum|_group_D|Cerebrooculofacioskeletal_syndrome_2|Xeroderma_pigmentosum|not_provided": 1,
    "not_provided|ERCC2-related_disorder": 1,
    "Xeroderma_pigmentosum|_group_D|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities": 1,
    "PPP1R13L-associated_cardiac_phenotype": 1,
    "Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities|Cardio-cutaneous_syndrome": 1,
    "Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities": 3,
    "Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities|Primary_dilated_cardiomyopathy": 1,
    "Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities|Multiple_congenital_anomalies/dysmorphic_syndrome": 1,
    "Primary_dilated_cardiomyopathy|Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities|Orofacial_cleft": 1,
    "OMIM:607463|Arrhythmogenic_cardiomyopathy_with_variable_ectodermal_abnormalities": 1,
    "Inborn_genetic_diseases|Cardiovascular_phenotype|PPP1R13L-related_disorder": 1,
    "PPP1R13L-related_disorder|not_specified": 1,
    "not_provided|not_specified|Cerebrooculofacioskeletal_syndrome_4|ERCC1-related_disorder": 1,
    "ERCC1-related_disorder": 4,
    "Cerebrooculofacioskeletal_syndrome_4": 7,
    "not_provided|not_specified|Cerebrooculofacioskeletal_syndrome_4": 1,
    "Cerebrooculofacioskeletal_syndrome_4|not_provided": 1,
    "Cerebrooculofacioskeletal_syndrome_4|not_provided|ERCC1-related_disorder": 1,
    "Cockayne_syndrome|Cerebrooculofacioskeletal_syndrome_4": 1,
    "Global_proximal_tubulopathy|Failure_to_thrive|Cholestatic_liver_disease|Premature_ovarian_insufficiency|Cutaneous_photosensitivity": 1,
    "Global_proximal_tubulopathy|Cholestatic_liver_disease|Failure_to_thrive|Premature_ovarian_insufficiency|Cutaneous_photosensitivity|not_provided": 1,
    "ERCC1-related_disorder|not_provided": 1,
    "not_provided|Cerebrooculofacioskeletal_syndrome_4": 3,
    "not_provided|ERCC1-related_disorder": 1,
    "Thyroid_hormone_metabolism|_abnormal|_3|Thyroid_hormone_metabolism|_abnormal_1": 1,
    "Hereditary_spastic_paraplegia_12": 18,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_12": 1,
    "Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia_12": 2,
    "Spastic_paraplegia|RTN2-related_disorder|Hereditary_spastic_paraplegia_12|not_provided": 1,
    "not_specified|Spastic_paraplegia|_autosomal_dominant|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "RTN2-related_disorder": 3,
    "RTN2-related_disorder|Spastic_paraplegia": 2,
    "Hereditary_spastic_paraplegia_12|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_12|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|_autosomal_dominant|Spastic_paraplegia|not_provided": 1,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia_12": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia": 1,
    "not_provided|Hereditary_spastic_paraplegia_12": 2,
    "not_specified|not_provided|Hereditary_spastic_paraplegia|Spastic_paraplegia|_autosomal_dominant|Spastic_paraplegia": 1,
    "Spastic_paraplegia|_autosomal_dominant|not_specified|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 1,
    "RTN2-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia_12|Spastic_paraplegia": 3,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia_12|not_provided": 1,
    "Hereditary_spastic_paraplegia_12|Spastic_paraplegia|not_provided": 1,
    "Hereditary_spastic_paraplegia_12|not_provided": 2,
    "Spastic_paraplegia|Hereditary_spastic_paraplegia|not_specified|not_provided": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_11|_with_spasticity": 3,
    "RTN2-related_disorder|not_specified|not_provided|Spastic_paraplegia": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_recessive_11|_with_spasticity|Hereditary_spastic_paraplegia_12": 1,
    "3-Methylglutaconic_aciduria_type_3": 49,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3": 116,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3|not_provided": 19,
    "Inborn_genetic_diseases|3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3": 3,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|not_provided": 16,
    "OPA3-related_disorder": 4,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 272,
    "Optic_Atrophy|_Dominant|3-Methylglutaconic_aciduria_type_3": 10,
    "3-Methylglutaconic_aciduria_type_3|not_provided|Optic_atrophy_3": 4,
    "not_provided|3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3": 13,
    "not_provided|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 18,
    "not_provided|3-Methylglutaconic_aciduria_type_3|Optic_Atrophy|_Dominant": 1,
    "Optic_atrophy_3|not_provided|3-Methylglutaconic_aciduria_type_3": 3,
    "Optic_Atrophy|_Dominant|3-Methylglutaconic_aciduria_type_3|not_provided": 2,
    "3-Methylglutaconic_aciduria_type_3|Optic_Atrophy|_Dominant": 8,
    "3-Methylglutaconic_aciduria_type_3|Optic_Atrophy|_Dominant|not_provided": 2,
    "not_specified|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3|not_provided": 1,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3|not_specified": 3,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|Inborn_genetic_diseases": 1,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3|Inborn_genetic_diseases": 3,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|OPA3-related_disorder|not_provided": 1,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria|3-Methylglutaconic_aciduria_type_3": 1,
    "Inborn_genetic_diseases|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 4,
    "OPA3-related_disorder|not_provided|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 1,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|not_specified|not_provided": 1,
    "not_provided|3-Methylglutaconic_aciduria_type_3|Inborn_genetic_diseases|Optic_atrophy_3": 1,
    "OPA3-related_disorder|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 2,
    "OPA3-related_disorder|not_specified|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 1,
    "Optic_atrophy_3": 4,
    "not_specified|Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3": 2,
    "not_provided|3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|not_specified": 1,
    "OPA3-related_disorder|3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3": 2,
    "not_specified|3-Methylglutaconic_aciduria_type_3": 1,
    "Inborn_genetic_diseases|Achromatopsia|3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3": 1,
    "not_provided|3-Methylglutaconic_aciduria_type_3": 1,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|not_specified|not_provided|See_cases|OPA3-related_disorder": 1,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3|Optic_atrophy": 1,
    "Foveal_hypoplasia": 1,
    "Optic_atrophy_3|3-Methylglutaconic_aciduria_type_3|OPA3-related_disorder|not_provided": 1,
    "3-Methylglutaconic_aciduria_type_3|Optic_atrophy_3|not_provided|not_specified": 1,
    "Branchiootorenal_syndrome_2": 84,
    "Branchiootorenal_syndrome_2|not_provided": 17,
    "Branchiootorenal_syndrome_2|not_specified": 8,
    "not_specified|not_provided|Branchiootorenal_syndrome_2": 2,
    "SIX5-related_disorder|not_provided": 7,
    "Branchiootorenal_syndrome_2|not_specified|not_provided": 4,
    "SIX5-related_disorder": 15,
    "SIX5-related_disorder|not_specified|not_provided|Branchiootorenal_syndrome_2": 1,
    "Branchiootorenal_syndrome_2|not_provided|not_specified": 4,
    "Branchiootorenal_syndrome_2|SIX5-related_disorder": 1,
    "not_specified|Branchiootorenal_syndrome_2|not_provided": 3,
    "not_provided|not_specified|SIX5-related_disorder": 2,
    "not_provided|Branchiootorenal_syndrome_2": 18,
    "not_provided|Branchiootorenal_syndrome_2|not_specified": 2,
    "not_specified|SIX5-related_disorder|not_provided": 1,
    "SIX5-related_disorder|Branchiootorenal_syndrome_2": 2,
    "not_provided|SIX5-related_disorder": 5,
    "SIX5-related_disorder|not_provided|Branchiootorenal_syndrome_2|not_specified": 1,
    "not_provided|not_specified|Branchiootorenal_syndrome_2": 2,
    "SIX5-related_disorder|not_provided|Branchiootorenal_syndrome_2": 1,
    "not_specified|Branchiootorenal_syndrome_2": 3,
    "Branchiootorenal_syndrome_2|not_provided|not_specified|SIX5-related_disorder": 2,
    "SIX5-related_disorder|not_specified": 2,
    "Branchiootorenal_syndrome_2|not_provided|SIX5-related_disorder": 1,
    "SIX5-related_disorder|Branchiootorenal_syndrome_2|not_provided": 2,
    "not_specified|not_provided|SIX5-related_disorder": 1,
    "SIX5-related_disorder|not_specified|not_provided": 1,
    "Steinert_myotonic_dystrophy_syndrome": 195,
    "Steinert_myotonic_dystrophy_syndrome|not_provided": 1,
    "DMPK-related_disorder|Inborn_genetic_diseases": 1,
    "DMPK-related_disorder": 13,
    "Myotonic_dystrophy|Inborn_genetic_diseases": 1,
    "Steinert_myotonic_dystrophy_syndrome|Inborn_genetic_diseases": 1,
    "Myotonic_dystrophy|not_provided|DMPK-related_disorder": 1,
    "Inborn_genetic_diseases|Steinert_myotonic_dystrophy_syndrome": 2,
    "not_specified|not_provided|DMPK-related_disorder": 1,
    "Myotonic_dystrophy": 1,
    "not_provided|not_specified|Steinert_myotonic_dystrophy_syndrome": 1,
    "DMWD-related_disorder": 11,
    "FOXA3-related_disorder": 7,
    "NOVA2-related_disorder": 9,
    "Inborn_genetic_diseases|NOVA2-related_disorder": 1,
    "Neurodevelopmental_disorder_with_or_without_autistic_features_and/or_structural_brain_abnormalities": 13,
    "not_provided|Neurodevelopmental_disorder_with_or_without_autistic_features_and/or_structural_brain_abnormalities": 3,
    "Neurodevelopmental_disorder_with_or_without_autistic_features_and/or_structural_brain_abnormalities|Intellectual_disability|_severe": 1,
    "not_provided|NOVA2-related_disorder|Neurodevelopmental_disorder_with_or_without_autistic_features_and/or_structural_brain_abnormalities": 1,
    "Neurodevelopmental_disorder_with_or_without_autistic_features_and/or_structural_brain_abnormalities|Inborn_genetic_diseases": 1,
    "NOVA2-related_disorder|not_provided": 1,
    "PPP5C-related_disorder": 5,
    "not_provided|PPP5C-related_disorder": 1,
    "3M_syndrome_3": 18,
    "not_provided|CCDC8-related_disorder": 2,
    "not_provided|not_specified|CCDC8-related_disorder": 1,
    "not_provided|3M_syndrome_3": 1,
    "3M_syndrome_3|not_provided": 3,
    "CCDC8-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Immunodeficiency|Inborn_genetic_diseases|not_provided": 1,
    "CCDC8-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|3M_syndrome_3|not_provided": 1,
    "not_provided|3M_syndrome_3|CCDC8-related_disorder": 1,
    "not_provided|Long_QT_syndrome_16": 2,
    "Long_QT_syndrome_16|Long_QT_syndrome_1|Congenital_long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome_1|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_1|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_1|Long_QT_syndrome_16": 3,
    "Cardiovascular_phenotype|CALM3-related_disorder|Long_QT_syndrome_1|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome_1|not_provided": 2,
    "not_provided|Long_QT_syndrome_1|CALM3-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Long_QT_syndrome_16": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome_1|Long_QT_syndrome_16": 1,
    "Long_QT_syndrome_16|Cardiovascular_phenotype|Long_QT_syndrome_1": 1,
    "Progressive_spastic_paraparesis|Intellectual_disability": 1,
    "PRKD2-related_disorder": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 2,
    "FKRP-related_disorder": 2,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 2,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided": 1,
    "not_provided|FKRP-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 48,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 13,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_specified|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 22,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype": 7,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 18,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 25,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Primary_dilated_cardiomyopathy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|not_specified|not_provided|Cardiovascular_phenotype|Dystrophin_deficiency": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 2,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 5,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 7,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_specified|not_provided": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 4,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 6,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 2,
    "not_provided|Cardiovascular_phenotype|not_specified|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided": 1,
    "Cardiomyopathy|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 2,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 3,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 6,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_specified|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "FKRP-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "not_specified|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Cardiovascular_phenotype|FKRP-related_disorder|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "FKRP-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_a|_10|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A|_4": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 2,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 3,
    "Walker-Warburg_congenital_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Myopathy_caused_by_variation_in_FKRP": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|not_specified|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|Hereditary_skeletal_muscle_disorder|FKRP-related_disorder|Myopathy_caused_by_variation_in_FKRP|Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_muscular_dystrophy-dystroglycanopathy|Nizon-Isidor_syndrome|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Limb-girdle_muscular_dystrophy|Myopathy|Neuronopathy|_distal_hereditary_motor|_type_2B|Scapular_winging|Difficulty_standing|Paresthesia|Difficulty_climbing_stairs|Difficulty_walking|Gait_imbalance|Muscle_weakness|Headache": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "FKRP-related_disorder|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|FKRP-related_disorder": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_without_impaired_intellectual_development)|_type_B|_5": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Abnormality_of_the_musculature|Walker-Warburg_congenital_muscular_dystrophy": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Myopathy_caused_by_variation_in_FKRP": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Myopathy_caused_by_variation_in_FKRP|Muscular_dystrophy-dystroglycanopathy_type_B5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_type_B5|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 2,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided": 1,
    "not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5": 1,
    "not_provided|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "Cardiovascular_phenotype|not_specified|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Intellectual_disability|Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Cardiovascular_phenotype": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_without_impaired_intellectual_development)|_type_B|_5": 1,
    "not_provided|FKRP-related_disorder|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|FKRP-related_disorder|not_specified|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_specified|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided|not_specified|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_specified": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|FKRP-related_disorder": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|not_provided|Cardiovascular_phenotype": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5": 1,
    "not_specified|Walker-Warburg_congenital_muscular_dystrophy|not_provided|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_without_impaired_intellectual_development)|_type_B|_5": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Cardiovascular_phenotype": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B5|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B5": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_without_impaired_intellectual_development)|_type_B|_5": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "FKRP-related_disorder|Cardiovascular_phenotype|not_provided|Walker-Warburg_congenital_muscular_dystrophy|not_specified|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Autosomal_recessive_limb-girdle_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Cardiovascular_phenotype|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Muscular_dystrophy-dystroglycanopathy_type_B5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A5|Muscular_dystrophy-dystroglycanopathy_type_B5|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I|Walker-Warburg_congenital_muscular_dystrophy|not_provided": 1,
    "not_provided|Walker-Warburg_congenital_muscular_dystrophy|Autosomal_recessive_limb-girdle_muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy|Autosomal_recessive_limb-girdle_muscular_dystrophy_type_2I": 1,
    "SLC1A5-related_disorder": 9,
    "Familial_hypocalciuric_hypercalcemia_3": 2,
    "not_provided|Familial_hypocalciuric_hypercalcemia_3": 6,
    "Familial_hypocalciuric_hypercalcemia_3|not_provided": 5,
    "not_specified|not_provided|AP2S1-related_disorder": 1,
    "AP2S1-related_disorder": 2,
    "Familial_hypocalciuric_hypercalcemia_3|not_provided|AP2S1-related_disorder": 1,
    "AP2S1-related_disorder|not_provided|Familial_hypocalciuric_hypercalcemia_3": 1,
    "AP2S1-related_disorder|Familial_hypocalciuric_hypercalcemia_3|not_provided": 1,
    "AP2S1-related_disorder|not_provided|Neurodevelopmental_disorder|Inborn_genetic_diseases|Familial_hypocalciuric_hypercalcemia_3": 1,
    "ARHGAP35-related_condition": 2,
    "Unilateral_microphthalmos": 1,
    "ZC3H4-related_disorder": 32,
    "ZC3H4-related_disorder|not_provided": 4,
    "not_provided|ZC3H4-related_disorder": 3,
    "C5AR1-related_disorder": 4,
    "C5AR1-related_disorder|not_specified": 1,
    "not_specified|C5AR1-related_disorder": 1,
    "C5AR1-related_disorder|not_provided": 1,
    "DHX34-related_disorder": 19,
    "DHX34-related_disorder|not_provided": 6,
    "not_specified|not_provided|DHX34-related_disorder": 1,
    "Intellectual_disability|Neurodevelopmental_delay|Reduced_renal_corticomedullary_differentiation|Emphysema|Postaxial_polydactyly|Polycystic_kidney_disease|Neurodevelopmental_disorders": 1,
    "Predisposition_to_thrombocytopenia": 1,
    "Intellectual_disability|Short_stature|Neurodevelopmental_delay|Microcephaly|Unilateral_renal_agenesis|Neurodevelopmental_disorders": 1,
    "not_provided|DHX34-related_disorder": 8,
    "not_specified|Predisposition_to_thrombocytopenia": 1,
    "not_specified|DHX34-associated_thromobocytopenia": 1,
    "not_specified|DHX34-related_disorder": 1,
    "Neurodevelopmental_disorder|Neurodevelopmental_delay|Seizure|Intellectual_disability|Neurodevelopmental_disorders": 1,
    "Predisposition_to_thrombocytopenia|DHX34-related_Neurodevelopmental_Disorder": 1,
    "Intellectual_disability|_moderate|Seizure": 2,
    "not_specified|Macrocephaly-developmental_delay_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Macrocephaly-developmental_delay_syndrome": 9,
    "not_provided|Macrocephaly-developmental_delay_syndrome": 7,
    "Macrocephaly-developmental_delay_syndrome|not_provided|KPTN-related_disorder": 2,
    "not_specified|Macrocephaly-developmental_delay_syndrome|not_provided": 1,
    "KPTN-related_disorder|Macrocephaly-developmental_delay_syndrome": 4,
    "Macrocephaly-developmental_delay_syndrome|Inborn_genetic_diseases": 2,
    "Macrocephaly-developmental_delay_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Macrocephaly-developmental_delay_syndrome": 1,
    "KPTN-related_disorder|Macrocephaly-developmental_delay_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Inborn_genetic_diseases|Macrocephaly-developmental_delay_syndrome": 1,
    "not_provided|Macrocephaly-developmental_delay_syndrome|KPTN-related_disorder|not_specified": 1,
    "Macrocephaly-developmental_delay_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Macrocephaly-developmental_delay_syndrome": 1,
    "Macrocephaly-developmental_delay_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "KPTN-related_disorder": 3,
    "not_specified|KPTN-related_disorder|Inborn_genetic_diseases|Macrocephaly-developmental_delay_syndrome|not_provided": 1,
    "Macrocephaly-developmental_delay_syndrome|not_provided|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Macrocephaly-developmental_delay_syndrome": 1,
    "Coffin-Siris_syndrome_12": 50,
    "BICRA-related_disorder": 11,
    "not_provided|BICRA-related_disorder": 3,
    "not_specified|not_provided|Coffin-Siris_syndrome_12": 1,
    "not_specified|BICRA-related_disorder": 3,
    "BICRA-related_disorder|Coffin-Siris_syndrome_12": 1,
    "not_specified|Coffin-Siris_syndrome_12": 3,
    "not_provided|Coffin-Siris_syndrome_12": 3,
    "BICRA-related_disorder|not_provided": 1,
    "CSS12_+_schizoaffective_disorder|_bipolar_type/adult-onset_psychiatric_condition": 1,
    "BICRA-related_disorder|not_specified|not_provided": 1,
    "Coffin-Siris_syndrome_12|not_specified": 1,
    "Intellectual_disability|Coffin-Siris_syndrome_12": 1,
    "not_provided|not_specified|BICRA-related_disorder": 1,
    "BICRA-related_disorder|not_specified": 2,
    "Retinitis_Pigmentosa|_Dominant|not_provided|Leber_congenital_amaurosis|Cone-Rod_Dystrophy|_Dominant": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinitis_pigmentosa": 28,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 27,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 72,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinal_dystrophy|CRX-related_disorder": 1,
    "not_provided|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 6,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 146,
    "Retinal_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 2,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinal_dystrophy": 5,
    "Inborn_genetic_diseases|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 2,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_specified": 1,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinal_dystrophy": 5,
    "Inborn_genetic_diseases|Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Inborn_genetic_diseases": 3,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided": 7,
    "not_specified|not_provided|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_provided": 2,
    "Retinal_dystrophy|Cone-rod_dystrophy_2": 2,
    "CRX-related_disorder|not_specified|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "not_provided|Retinal_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_provided|Retinitis_pigmentosa|Cone-rod_dystrophy": 1,
    "CRX-related_disorder|Inborn_genetic_diseases|Retinal_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided|Cone-rod_dystrophy": 1,
    "Cone-rod_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 5,
    "Leber_congenital_amaurosis_7": 11,
    "Retinal_dystrophy|not_specified|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_1": 1,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinal_dystrophy|not_provided": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|maculopathy|not_provided": 1,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_provided": 2,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided|Retinitis_pigmentosa": 8,
    "Retinal_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided": 1,
    "not_provided|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 2,
    "Autosomal_dominant_retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 14,
    "Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_provided": 1,
    "Retinal_dystrophy|not_specified|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided|Central_core_myopathy|Retinitis_pigmentosa": 1,
    "Inborn_genetic_diseases|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 2,
    "CRX-related_disorder|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Inborn_genetic_diseases": 6,
    "Autosomal_dominant_retinitis_pigmentosa|CRX-related_disorder|Retinal_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided|Retinitis_pigmentosa|Leber_congenital_amaurosis_1": 1,
    "not_provided|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Benign_concentric_annular_macular_dystrophy": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "not_specified|Retinal_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinitis_pigmentosa|not_provided": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_1|Inborn_genetic_diseases": 1,
    "not_provided|Leber_congenital_amaurosis_7": 2,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|See_cases": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_specified|not_provided": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinitis_pigmentosa|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Stargardt_disease": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Inborn_genetic_diseases|Retinal_dystrophy": 1,
    "CRX-related_disorder|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_provided|Retinitis_pigmentosa": 1,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinitis_pigmentosa": 4,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Retinal_dystrophy|CRX-related_disorder|not_specified|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Leber_congenital_amaurosis_7|not_provided": 1,
    "Benign_concentric_annular_macular_dystrophy|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2": 1,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Benign_concentric_annular_macular_dystrophy": 1,
    "not_provided|Retinal_dystrophy|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "Leber_congenital_amaurosis_7|not_provided|Autosomal_dominant_retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|not_specified|Leber_congenital_amaurosis_1|not_provided": 1,
    "CRX-related_disorder": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|CRX-related_disorder": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Inborn_genetic_diseases": 1,
    "Retinitis_pigmentosa|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|not_provided": 3,
    "Leber_congenital_amaurosis_7|Retinitis_pigmentosa|Cone-rod_dystrophy_2": 8,
    "Leber_congenital_amaurosis|Cone-Rod_Dystrophy|_Dominant|Retinitis_Pigmentosa|_Dominant|not_provided": 4,
    "Retinitis_pigmentosa|Leber_congenital_amaurosis_7|not_provided|Cone-rod_dystrophy_2": 1,
    "Cone-rod_dystrophy_2|Retinitis_pigmentosa|Leber_congenital_amaurosis_7|not_provided": 2,
    "not_provided|Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinitis_pigmentosa": 1,
    "Leber_congenital_amaurosis_7|Retinitis_pigmentosa|Cone-rod_dystrophy_2|not_provided": 3,
    "Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7": 1,
    "Leber_congenital_amaurosis_7|Retinitis_pigmentosa|not_provided|Cone-rod_dystrophy_2": 1,
    "Cone-rod_dystrophy_2|Retinitis_pigmentosa|not_provided|Leber_congenital_amaurosis_7": 2,
    "Leber_congenital_amaurosis_7|Cone-rod_dystrophy_2|Retinitis_pigmentosa|not_provided": 12,
    "Leber_congenital_amaurosis|Cone-Rod_Dystrophy|_Dominant|Retinitis_Pigmentosa|_Dominant": 3,
    "Cone-rod_dystrophy_2|Leber_congenital_amaurosis_7|Retinitis_pigmentosa|not_provided": 2,
    "not_provided|LIG1-related_disorder": 12,
    "LIG1-related_disorder|not_provided": 8,
    "DNA_Ligase_I_Deficiency|LIG1-related_disorder|not_provided": 1,
    "Immunodeficiency_96": 6,
    "Immunodeficiency_96|not_specified|not_provided": 1,
    "not_provided|Immunodeficiency_96": 5,
    "Immunodeficiency_96|DNA_Ligase_I_Deficiency|not_provided": 1,
    "not_provided|LIG1-related_disorder|not_specified": 1,
    "Immunodeficiency_96|not_provided": 1,
    "Immunodeficiency_96|not_specified": 1,
    "LIG1-related_disorder": 2,
    "not_specified|Immunodeficiency_96|not_provided": 1,
    "not_specified|Immunodeficiency_96": 1,
    "Inflammatory_bowel_disease_30": 5,
    "not_provided|CARD8-related_disorder": 3,
    "not_specified|CARD8-related_disorder|not_provided": 1,
    "not_specified|not_provided|CARD8-related_disorder|Inflammatory_bowel_disease_30": 1,
    "CARD8-related_disorder|not_specified|not_provided": 1,
    "not_provided|CARD8-related_disorder|not_specified": 1,
    "not_provided|Inflammatory_bowel_disease_30": 1,
    "CARD8-related_disorder|not_provided": 3,
    "Inflammatory_bowel_disease_30|not_provided": 1,
    "CARD8-related_disorder|not_provided|not_specified": 1,
    "CARD8-related_disorder": 2,
    "not_specified|Inflammatory_bowel_disease_30": 1,
    "not_specified|CARD8-related_disorder": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_20": 7,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_20|ODAD1-related_disorder": 1,
    "Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia": 3,
    "not_provided|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia|not_specified": 1,
    "ODAD1-related_disorder|Primary_ciliary_dyskinesia": 4,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Primary_ciliary_dyskinesia_20": 2,
    "not_provided|not_specified|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia|ODAD1-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_20": 5,
    "not_provided|Primary_ciliary_dyskinesia_20": 1,
    "Primary_ciliary_dyskinesia_20": 6,
    "Primary_ciliary_dyskinesia|ODAD1-related_disorder": 4,
    "not_specified|not_provided|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia": 2,
    "Adams-Oliver_syndrome_5|Primary_ciliary_dyskinesia_20": 1,
    "ODAD1-related_disorder": 3,
    "ODAD1-related_disorder|Adams-Oliver_syndrome_5|not_provided|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "not_provided|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia": 1,
    "Fraser_syndrome_3|not_specified|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_20": 1,
    "ODAD1-related_disorder|Primary_ciliary_dyskinesia_20|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_20|not_provided|Primary_ciliary_dyskinesia": 2,
    "Developmental_and_epileptic_encephalopathy|_46|not_provided": 19,
    "GRIN2D-related_disorder": 18,
    "not_provided|GRIN2D-related_disorder": 6,
    "not_provided|Developmental_and_epileptic_encephalopathy|_46": 9,
    "Developmental_and_epileptic_encephalopathy|_46": 53,
    "GRIN2D-related_disorder|not_provided": 9,
    "GRIN2D-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_46": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_46": 1,
    "Developmental_and_epileptic_encephalopathy|_46|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_46|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_46|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|GRIN2D-related_disorder": 2,
    "not_provided|Intellectual_disability|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_46": 1,
    "Developmental_and_epileptic_encephalopathy|_46|not_provided|GRIN2D-related_disorder": 1,
    "GRIN2D-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_46|not_provided": 1,
    "GRWD1-related_disorder": 10,
    "GRWD1-related_disorder|not_specified": 1,
    "Diarrhea_14|_congenital|Congenital_diarrhea": 2,
    "LMTK3-related_disorder": 2,
    "SULT2B1-related_disorder|not_provided": 6,
    "Ichthyosis|_congenital|_autosomal_recessive_14|Autosomal_recessive_congenital_ichthyosis_2": 2,
    "not_provided|SULT2B1-related_disorder": 4,
    "SULT2B1-related_disorder": 1,
    "Ichthyosis|_congenital|_autosomal_recessive_14": 2,
    "Ichthyosis|_congenital|_autosomal_recessive_14|Autosomal_recessive_congenital_ichthyosis_1": 1,
    "not_provided|Ichthyosis|_congenital|_autosomal_recessive_14": 2,
    "Autosomal_recessive_congenital_ichthyosis_2|Ichthyosis|_congenital|_autosomal_recessive_14": 1,
    "Diamond-Blackfan_anemia_18": 3,
    "not_provided|Diamond-Blackfan_anemia_18": 1,
    "RPL18-related_disorder|not_provided": 5,
    "not_provided|RPL18-related_disorder": 1,
    "RPL18-related_disorder": 2,
    "not_provided|Fucosyltransferase_6_deficiency|Familial_Otitis_Media": 1,
    "FUT2-related_disorder": 2,
    "Familial_Otitis_Media": 5,
    "FUT2-related_disorder|not_provided": 2,
    "SECRETOR/NONSECRETOR_POLYMORPHISM|_JAPANESE_TYPE|Familial_Otitis_Media|not_provided": 1,
    "VITAMIN_B12_PLASMA_LEVEL_QUANTITATIVE_TRAIT_LOCUS_1|Bombay_phenotype|SECRETOR/NONSECRETOR_POLYMORPHISM|Familial_Otitis_Media|not_provided": 1,
    "Bombay_phenotype|Familial_Otitis_Media|VITAMIN_B12_PLASMA_LEVEL_QUANTITATIVE_TRAIT_LOCUS_1": 1,
    "Bombay_phenotype": 2,
    "Familial_Otitis_Media|Levothyroxine_response": 1,
    "RASIP1-related_disorder": 2,
    "FUT1-related_disorder": 4,
    "Para-Bombay_phenotype": 3,
    "BOMBAY_PHENOTYPE|_DIGENIC|Bombay_phenotype": 1,
    "Bombay_phenotype|not_specified": 1,
    "not_provided|BCAT2-related_disorder": 1,
    "Hypervalinemia_and_hyperleucine-isoleucinemia|not_provided": 2,
    "BCAT2-related_disorder|not_provided": 1,
    "Hypervalinemia_and_hyperleucine-isoleucinemia": 6,
    "Inborn_genetic_diseases|Carcinoma_of_colon": 1,
    "T-cell_acute_lymphoblastic_leukemia": 2,
    "FTL-related_disorder|not_provided": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 104,
    "Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|not_provided": 3,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|not_provided|FTL-related_disorder": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|FTL-related_disorder|not_provided|Neuroferritinopathy": 1,
    "FTL-related_disorder|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|not_provided": 1,
    "Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts": 14,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|L-ferritin_deficiency|not_provided": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|not_provided": 3,
    "not_provided|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 2,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|L-ferritin_deficiency": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|FTL-related_disorder": 2,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|L-ferritin_deficiency|not_specified|not_provided": 1,
    "L-ferritin_deficiency|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|FTL-related_disorder": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|FTL-related_disorder|not_provided": 1,
    "not_provided|Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|Inborn_genetic_diseases": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|sporadic_abdominal_aortic_aneurysm|L-ferritin_deficiency|not_specified|not_provided|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 1,
    "Neuroferritinopathy|not_provided|sporadic_abdominal_aortic_aneurysm|FTL-related_disorder|Hereditary_hyperferritinemia_with_congenital_cataracts|not_specified": 1,
    "not_specified|not_provided|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|FTL-related_disorder|not_provided": 1,
    "Neuroferritinopathy": 9,
    "L-FERRITIN_DEFICIENCY|_AUTOSOMAL_RECESSIVE|Inborn_genetic_diseases": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|not_specified": 1,
    "Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "Inborn_genetic_diseases|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|Inborn_genetic_diseases|FTL-related_disorder": 1,
    "not_specified|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy|not_provided": 1,
    "FTL-related_disorder": 3,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|not_provided|Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts": 3,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 430,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|FTL-related_disorder|Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts": 1,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|not_provided|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 4,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|FTL-related_disorder|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "Neuroferritinopathy|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|Hereditary_hyperferritinemia_with_congenital_cataracts": 1,
    "Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 1,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 2,
    "not_provided|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 28,
    "Inborn_genetic_diseases|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 47,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|GYS1-related_disorder|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 4,
    "GYS1-related_disorder": 2,
    "not_provided|GYS1-related_disorder|not_specified|Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 8,
    "not_specified|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|not_provided|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "not_specified|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 13,
    "GYS1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|GYS1-related_disorder|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 2,
    "GYS1-related_disorder|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 11,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|not_provided": 5,
    "not_provided|not_specified|Neuroferritinopathy|Hereditary_hyperferritinemia_with_congenital_cataracts|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 1,
    "Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|GYS1-related_disorder|not_provided|Hereditary_hyperferritinemia_with_congenital_cataracts|Neuroferritinopathy": 1,
    "GYS1-related_disorder|not_specified|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 1,
    "not_specified|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|not_provided": 1,
    "not_specified|not_provided|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 6,
    "Inborn_genetic_diseases|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|not_provided": 1,
    "Glycogen_storage_disease": 1,
    "not_provided|GYS1-related_disorder|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 2,
    "not_provided|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency|Inborn_genetic_diseases": 1,
    "GYS1-related_disorder|Inborn_genetic_diseases|Glycogen_storage_disease_due_to_muscle_and_heart_glycogen_synthase_deficiency": 1,
    "not_provided|Isolated_lutropin_deficiency|Variant_of_unknown_significance": 1,
    "not_provided|Isolated_lutropin_deficiency": 7,
    "not_provided|LHB-related_disorder": 2,
    "LHB-related_disorder|not_provided": 1,
    "Isolated_lutropin_deficiency": 6,
    "Isolated_lutropin_deficiency|not_provided": 2,
    "Glaucoma_1|_open_angle|_O": 1,
    "not_provided|Glaucoma_1|_open_angle|_O": 1,
    "NTF4-related_disorder": 1,
    "not_provided|Glaucoma_1|_open_angle|_O|Intellectual_disability|_X-linked_99": 1,
    "NTF4-related_disorder|not_provided": 1,
    "LIN7B-related_disorder|not_provided": 1,
    "LIN7B-related_disorder": 2,
    "not_provided|PAUL-CHAO_NEURODEVELOPMENTAL_SYNDROME": 1,
    "PPFIA3-related_disorder": 6,
    "PPFIA3-associated_neurodevelopmental_disorder": 2,
    "not_provided|PAUL-CHAO_NEURODEVELOPMENTAL_SYNDROME|PPFIA3-related_disorder": 1,
    "PAUL-CHAO_NEURODEVELOPMENTAL_SYNDROME|PPFIA3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|PPFIA3-related_disorder": 1,
    "not_provided|PPFIA3-related_disorder": 1,
    "PPFIA3-related_disorder|not_provided": 1,
    "PAUL-CHAO_NEURODEVELOPMENTAL_SYNDROME|not_provided|Neurodevelopmental_delay": 1,
    "not_provided|Progressive_familial_heart_block": 1,
    "not_specified|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB": 719,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 184,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|not_provided": 5,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_specified": 3,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 186,
    "TRPM4-related_disorder|Progressive_familial_heart_block_type_IB": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB": 4,
    "not_provided|Progressive_familial_heart_block_type_IB": 22,
    "not_specified|Progressive_familial_heart_block_type_IB": 4,
    "not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 13,
    "Progressive_familial_heart_block_type_IB|not_specified": 12,
    "Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_provided": 2,
    "Cardiovascular_phenotype|not_specified|Progressive_familial_heart_block_type_IB|not_provided": 3,
    "Progressive_familial_heart_block_type_IB|Inborn_genetic_diseases": 2,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_provided": 13,
    "not_specified|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 7,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "Progressive_familial_heart_block_type_IB|not_specified|not_provided": 3,
    "Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB|not_provided": 2,
    "Progressive_familial_heart_block_type_IB|not_provided": 20,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_provided|Cardiomyopathy": 1,
    "TRPM4-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "Cardiovascular_phenotype|TRPM4-related_disorder|not_specified|not_provided|Progressive_familial_heart_block_type_IB": 2,
    "Cardiovascular_phenotype|TRPM4-related_disorder|not_specified|not_provided|Brugada_syndrome|Progressive_familial_heart_block_type_IB": 1,
    "not_specified|Progressive_familial_heart_block_type_IB|not_provided|Cardiovascular_phenotype": 1,
    "Progressive_familial_heart_block_type_IB|not_specified|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_provided|not_specified|Progressive_familial_heart_block_type_IB": 1,
    "not_provided|Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_specified|not_provided": 6,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_provided": 17,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|Cardiovascular_phenotype|not_provided": 5,
    "not_specified|Progressive_familial_heart_block_type_IB|not_provided": 3,
    "Progressive_familial_heart_block_type_IB|TRPM4-related_disorder|Cardiovascular_phenotype": 2,
    "Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 8,
    "TRPM4-related_disorder": 7,
    "TRPM4-related_disorder|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_provided|Erythrokeratodermia_variabilis_et_progressiva_6": 2,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|not_provided": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6": 8,
    "Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block_type_IB": 15,
    "Short_QT_syndrome|Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB|not_provided": 1,
    "Cardiovascular_phenotype|TRPM4-related_disorder|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|not_provided|Erythrokeratodermia_variabilis_et_progressiva_6|Cardiovascular_phenotype": 2,
    "not_specified|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 2,
    "not_provided|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 15,
    "not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_specified|Cardiomyopathy": 1,
    "not_specified|Progressive_familial_heart_block_type_IB|not_provided|Cardiovascular_phenotype|TRPM4-related_disorder": 1,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6": 10,
    "TRPM4-related_disorder|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|Erythrokeratodermia_variabilis_et_progressiva_6": 6,
    "Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6": 2,
    "not_provided|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_specified": 1,
    "Progressive_familial_heart_block_type_IB|Brugada_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_specified|Progressive_familial_heart_block": 1,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|TRPM4-related_disorder|not_specified|not_provided": 1,
    "not_provided|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|Erythrokeratodermia_variabilis_et_progressiva_6": 2,
    "Progressive_familial_heart_block_type_IB|not_specified|Progressive_familial_heart_block|not_provided": 1,
    "Cardiac_arrest|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 1,
    "Progressive_familial_heart_block_type_IB|not_provided|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|Cardiovascular_phenotype|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB|not_provided": 2,
    "TRPM4-related_disorder|Cardiovascular_phenotype|not_specified|Progressive_familial_heart_block_type_IB": 1,
    "not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6": 2,
    "Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block_type_IB|not_specified": 2,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|Cardiovascular_phenotype": 9,
    "Brugada_syndrome|not_specified|Progressive_familial_heart_block_type_IB|not_provided|Progressive_familial_heart_block|_type_1A|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|not_specified": 3,
    "Cardiovascular_phenotype|not_specified|Progressive_familial_heart_block_type_IB|not_provided|TRPM4-related_disorder": 1,
    "Progressive_familial_heart_block_type_IB|TRPM4-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|not_provided|Brugada_syndrome": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|TRPM4-related_disorder": 1,
    "Progressive_familial_heart_block_type_IB|TRPM4-related_disorder": 1,
    "Sudden_cardiac_death|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Progressive_familial_heart_block_type_IB|not_provided": 1,
    "TRPM4-related_disorder|Cardiovascular_phenotype|Ventricular_fibrillation|Cardiomyopathy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_specified|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Progressive_familial_heart_block_type_IB|Progressive_familial_heart_block|_type_1A|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|not_provided|TRPM4-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Progressive_familial_heart_block_type_IB|not_provided": 1,
    "Sudden_cardiac_death|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 1,
    "Brugada_syndrome|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|not_provided|Cardiovascular_phenotype": 3,
    "not_specified|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_provided": 1,
    "Progressive_familial_heart_block_type_IB|not_specified|TRPM4-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|TRPM4-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|TRPM4-related_disorder|not_specified": 1,
    "not_provided|TRPM4-related_disorder|Cardiovascular_phenotype|not_specified|Progressive_familial_heart_block_type_IB": 1,
    "Ventricular_tachycardia|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 1,
    "Restrictive_cardiomyopathy|Cardiomyopathy|Progressive_familial_heart_block_type_IB|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 1,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|TRPM4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "TRPM4-related_disorder|Cardiovascular_phenotype": 1,
    "TRPM4-related_disorder|not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|not_specified|Long_QT_syndrome": 1,
    "not_provided|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|Wolff-Parkinson-White_pattern|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|TRPM4-related_disorder|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6|not_provided|Cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|TRPM4-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 1,
    "Progressive_familial_heart_block_type_IB|not_provided|not_specified": 1,
    "Progressive_familial_heart_block_type_IB|not_specified|Cardiovascular_phenotype": 3,
    "Erythrokeratodermia_variabilis_et_progressiva_6": 1,
    "Erythrokeratodermia_variabilis_et_progressiva_6|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "Cardiovascular_phenotype|Erythrokeratodermia_variabilis_et_progressiva_6|Progressive_familial_heart_block_type_IB": 1,
    "Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "not_provided|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6": 1,
    "Conduction_system_disorder|Progressive_familial_heart_block_type_IB|Long_QT_syndrome": 1,
    "TRPM4-related_disorder|Cardiovascular_phenotype|not_provided|Progressive_familial_heart_block_type_IB": 1,
    "Catecholaminergic_polymorphic_ventricular_tachycardia_1|Progressive_familial_heart_block_type_IB|Cardiovascular_phenotype": 1,
    "not_specified|Family_history_of_sudden_cardiac_death|not_provided|Cardiovascular_phenotype|Progressive_familial_heart_block_type_IB|Conduction_disorder_of_the_heart": 1,
    "not_specified|not_provided|Progressive_familial_heart_block_type_IB|Erythrokeratodermia_variabilis_et_progressiva_6": 1,
    "Spermatogenic_failure_88|Premature_ovarian_failure_22": 2,
    "Genetic_non-acquired_premature_ovarian_failure|Premature_ovarian_failure_22": 1,
    "KASH5-related_disorder": 1,
    "Immunodeficiency_125": 1,
    "PRR12-related_disorder": 57,
    "PRR12-related_disorder|not_provided": 13,
    "Neuroocular_syndrome": 18,
    "Neuroocular_syndrome_1": 18,
    "not_provided|PRR12-related_disorder": 14,
    "complex_microphthalmia": 3,
    "Neuroocular_syndrome|not_provided": 2,
    "Neuroocular_syndrome|Iris_coloboma|Abnormality_of_vision|Delayed_speech_and_language_development|Autism|Motor_delay": 1,
    "PRR12-related_neuroocular_syndrome": 1,
    "Inborn_genetic_diseases|PRR12-related_disorder": 5,
    "PRR12-associated_Intellectual_Disability": 1,
    "Neuroocular_syndrome|Iris_coloboma|Abnormality_of_vision|Delayed_speech_and_language_development|Autism|Motor_delay|Neuroocular_syndrome_1": 1,
    "Inborn_genetic_diseases|Neuroocular_syndrome_1": 1,
    "Neuroocular_syndrome_1|Inborn_genetic_diseases": 1,
    "PRR12-related_disorder|Neuroocular_syndrome_1": 1,
    "PRR12-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PRR12-related_disorder|Inborn_genetic_diseases": 3,
    "Neuroocular_syndrome_1|not_provided|Neuroocular_syndrome": 1,
    "Neuroocular_syndrome_1|Neuroocular_syndrome|not_provided": 1,
    "not_provided|Neuroocular_syndrome_1": 1,
    "not_provided|Neuroocular_syndrome": 1,
    "not_provided|PRR12-related_disorder|Inborn_genetic_diseases": 2,
    "Iris_coloboma|Abnormality_of_vision|Delayed_speech_and_language_development|Autism|Motor_delay|Neuroocular_syndrome_1": 1,
    "PPR12-associated_neurodevelopmental_disorder": 1,
    "not_provided|Inborn_genetic_diseases|PRR12-related_disorder": 1,
    "complex_microphthalmia|Neuroocular_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|PRR12-related_disorder": 1,
    "Neuroocular_syndrome_1|Neuroocular_syndrome": 1,
    "RRAS-related_disorder|not_specified": 1,
    "RRAS-related_disorder|not_specified|not_provided": 1,
    "Noonan_syndrome|not_specified": 30,
    "not_specified|RRAS-related_disorder|Noonan_syndrome": 1,
    "Noonan_syndrome|RRAS-related_disorder|not_specified": 2,
    "RRAS-related_disorder|Noonan_syndrome": 2,
    "Noonan_syndrome|not_specified|RRAS-related_disorder": 4,
    "not_provided|Noonan_syndrome|RRAS-related_disorder|not_specified": 2,
    "RRAS-related_disorder|Noonan_syndrome|not_specified": 2,
    "RRAS-related_disorder|not_provided|Noonan_syndrome": 1,
    "not_specified|not_provided|RRAS-related_disorder|Noonan_syndrome": 1,
    "not_specified|RRAS-related_disorder": 1,
    "Noonan_syndrome|Hereditary_cancer|not_specified": 1,
    "not_specified|Noonan_syndrome|not_provided": 1,
    "RRAS-related_disorder|not_specified|Noonan_syndrome": 1,
    "RRAS-related_disorder|not_provided|Noonan_syndrome|not_specified": 1,
    "not_provided|not_specified|Noonan_syndrome|RRAS-related_disorder": 1,
    "RRAS-related_disorder": 5,
    "not_specified|Noonan_syndrome|RRAS-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_26": 468,
    "IRF3-related_disorder": 9,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_7": 2,
    "IRF3-related_disorder|Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_7": 1,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_7|not_provided|IRF3-related_disorder": 2,
    "Encephalopathy|_acute|_infection-induced_(herpes-specific)|_susceptibility_to|_7|not_specified": 1,
    "IRF3-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia_73": 240,
    "not_specified|Hereditary_spastic_paraplegia_73": 16,
    "Hereditary_spastic_paraplegia_73|not_specified": 22,
    "Hereditary_spastic_paraplegia_73|not_provided|not_specified": 1,
    "CPT1C-related_disorder|Hereditary_spastic_paraplegia_73": 5,
    "Hereditary_spastic_paraplegia_73|CPT1C-related_disorder": 1,
    "Hereditary_spastic_paraplegia_73|not_provided": 8,
    "not_provided|Hereditary_spastic_paraplegia_73": 9,
    "Hereditary_spastic_paraplegia_73|not_provided|CPT1C-related_disorder": 2,
    "Hereditary_spastic_paraplegia_73|not_specified|not_provided": 1,
    "not_provided|Hereditary_spastic_paraplegia_73|CPT1C-related_disorder": 1,
    "Hereditary_spastic_paraplegia|Hereditary_spastic_paraplegia_73": 1,
    "CPT1C-related_disorder": 3,
    "CPT1C-related_disorder|not_specified|Hereditary_spastic_paraplegia_73": 1,
    "FUZ-related_disorder": 7,
    "FUZ-related_disorder|not_provided": 1,
    "not_specified|Neural_tube_defect": 1,
    "Neural_tube_defect|not_provided": 1,
    "not_specified|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome": 8,
    "Autism|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|MED25-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|not_specified|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided": 1,
    "MED25-related_disorder": 2,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|MED25-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2|Polyneuropathy": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_delay|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2B2|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_2|Tip-toe_gait": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "MED25-related_disorder|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2": 9,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Neurodevelopmental_delay": 1,
    "MED25-related_disorder|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome": 5,
    "Charcot-Marie-Tooth_disease_type_2B2|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "MED25-related_disorder|Charcot-Marie-Tooth_disease_type_2": 4,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2B2|Charcot-Marie-Tooth_disease_type_2": 2,
    "Charcot-Marie-Tooth_disease_type_2|not_provided|Charcot-Marie-Tooth_disease|not_specified|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome": 1,
    "Charcot-Marie-Tooth_disease_type_2|MED25-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_type_2|MED25-related_disorder": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2B2": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_2B2|not_provided": 1,
    "MED25-related_disorder|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2B2|Tip-toe_gait": 1,
    "Polyneuropathy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease_type_2B2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_type_2|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2B2|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_2B2|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2": 1,
    "Charcot-Marie-Tooth_disease_type_2|Tip-toe_gait": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_specified": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2B2|Charcot-Marie-Tooth_disease_type_2|not_provided|not_specified": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_2|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|not_provided|Charcot-Marie-Tooth_disease_type_2": 1,
    "MED25-related_disorder|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "Tip-toe_gait|Charcot-Marie-Tooth_disease_type_2|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "not_provided|Tip-toe_gait|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2": 1,
    "Congenital_cataract-microcephaly-nevus_flammeus_simplex-severe_intellectual_disability_syndrome|Charcot-Marie-Tooth_disease_type_2|Charcot-Marie-Tooth_disease|not_provided|not_specified|Polyneuropathy": 1,
    "not_provided|Microcephaly|_seizures|_and_developmental_delay": 2,
    "Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay|not_specified": 1,
    "Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified|Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|PNKP-related_disorder": 4,
    "Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases": 55,
    "Ataxia_-_oculomotor_apraxia_type_4": 3,
    "Charcot-Marie-Tooth_disease_type_2B2|Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12|Abnormal_cerebral_morphology|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_provided": 73,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 7,
    "PNKP-related_disorder|not_provided": 1,
    "PNKP-related_disorder": 6,
    "Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12": 5,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_12|not_provided|Microcephaly|_seizures|_and_developmental_delay": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12": 59,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases": 8,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Inborn_genetic_diseases": 1,
    "PNKP-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 7,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 2,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified": 26,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Inborn_genetic_diseases|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_12|not_provided|Inborn_genetic_diseases": 12,
    "Inborn_genetic_diseases|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_provided|Microcephaly|_seizures|_and_developmental_delay|PNKP-related_disorder|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12|not_provided": 8,
    "Developmental_and_epileptic_encephalopathy|_12|not_provided|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2|Microcephaly|_seizures|_and_developmental_delay": 2,
    "Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Pyridoxine-dependent_epilepsy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|not_specified": 4,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified|Microcephaly|_seizures|_and_developmental_delay": 2,
    "PNKP-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 1,
    "PNKP-related_disorder|Developmental_and_epileptic_encephalopathy|_12": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 1,
    "not_provided|Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Microcephaly|_seizures|_and_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases": 1,
    "Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_12": 20,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_12": 15,
    "Charcot-Marie-Tooth_disease_type_2B2": 2,
    "Developmental_and_epileptic_encephalopathy|_12|Charcot-Marie-Tooth_disease_type_2B2|not_provided|Inborn_genetic_diseases": 1,
    "Microcephaly|_seizures|_and_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12": 5,
    "Developmental_and_epileptic_encephalopathy|_12|PNKP-related_disorder|not_specified": 1,
    "not_specified|PNKP-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|PNKP-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "PNKP-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Ataxia|_early-onset|_with_oculomotor_apraxia_and_hypoalbuminemia": 1,
    "PNKP-related_disorder|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4": 1,
    "Microcephaly|_seizures|_and_developmental_delay|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|PNKP-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|not_provided": 7,
    "Inborn_genetic_diseases|Ataxia_-_oculomotor_apraxia_type_4|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Seizure|Abnormality_of_the_nervous_system|Intellectual_disability": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Abnormality_of_the_nervous_system|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|not_specified": 2,
    "Global_developmental_delay|Primary_microcephaly|Cerebellar_atrophy": 1,
    "Ataxia_-_oculomotor_apraxia_type_4|Developmental_and_epileptic_encephalopathy|_12|Charcot-Marie-Tooth_disease_type_2B2|Microcephaly|_seizures|_and_developmental_delay|not_provided": 1,
    "Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_12|Epileptic_encephalopathy|not_provided|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_12|not_provided|not_specified": 4,
    "Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_12|Ataxia_-_oculomotor_apraxia_type_4": 2,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 3,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 4,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|PNKP-related_disorder|not_specified": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|Ataxia_-_oculomotor_apraxia_type_4|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Ataxia_-_oculomotor_apraxia_type_4": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_12|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 4,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_12": 3,
    "PNKP-related_disorder|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|Charcot-Marie-Tooth_disease_type_2B2|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Abnormal_cerebral_morphology|Microcephaly": 1,
    "not_provided|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|Charcot-Marie-Tooth_disease_type_2B2|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases": 1,
    "Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay|not_specified": 1,
    "Abnormality_of_the_nervous_system|not_provided|Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12": 1,
    "PNKP-related_disorder|Inborn_genetic_diseases|Ataxia_-_oculomotor_apraxia_type_4|Developmental_and_epileptic_encephalopathy|_12|not_provided|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Inborn_genetic_diseases|PNKP-related_disorder|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "PNKP-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "PNKP-related_disorder|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Inborn_genetic_diseases": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 1,
    "not_provided|Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Ataxia_-_oculomotor_apraxia_type_4|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_provided|Microcephaly|_seizures|_and_developmental_delay": 1,
    "PNKP-related_disorder|Charcot-Marie-Tooth_disease_type_2B2|Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|not_provided": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_12|Ataxia_-_oculomotor_apraxia_type_4|not_specified": 1,
    "PNKP-related_disorder|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_12|not_provided|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2|not_specified": 1,
    "not_provided|PNKP-related_disorder|Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12|Charcot-Marie-Tooth_disease_type_2B2": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay|PNKP-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases": 2,
    "Charcot-Marie-Tooth_disease_type_2B2|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified|not_provided|Inborn_genetic_diseases|PNKP-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_2B2|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_provided|Microcephaly|_seizures|_and_developmental_delay|Ataxia_-_oculomotor_apraxia_type_4|not_specified|Charcot-Marie-Tooth_disease_type_2B2": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_type_2B2|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay|PNKP-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Inborn_genetic_diseases|Ataxia_-_oculomotor_apraxia_type_4|Charcot-Marie-Tooth_disease_type_2B2|Microcephaly|_seizures|_and_developmental_delay|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_specified|Microcephaly|_seizures|_and_developmental_delay|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_specified|PNKP-related_disorder": 1,
    "PNKP-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Ataxia_-_oculomotor_apraxia_type_4|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Ataxia_-_oculomotor_apraxia_type_4|Microcephaly|_seizures|_and_developmental_delay": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|Microcephaly|_seizures|_and_developmental_delay": 1,
    "Microcephaly|_seizures|_and_developmental_delay|not_specified": 2,
    "NUP62-related_disorder|not_provided": 4,
    "not_specified|not_provided|Infantile_bilateral_striatal_necrosis": 3,
    "Infantile_bilateral_striatal_necrosis": 1,
    "NUP62-related_disorder": 2,
    "NUP62-related_disorder|not_specified|not_provided|Infantile_bilateral_striatal_necrosis": 1,
    "Familial_infantile_bilateral_striatal_necrosis|not_provided": 2,
    "not_provided|NUP62-related_disorder": 4,
    "Infantile_bilateral_striatal_necrosis|not_provided": 1,
    "NUP62-related_disorder|not_specified|not_provided": 1,
    "Familial_infantile_bilateral_striatal_necrosis|not_provided|not_specified": 1,
    "Familial_infantile_bilateral_striatal_necrosis": 1,
    "NUP62-related_disorder|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A": 83,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified": 2,
    "not_provided|MYH14-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "MYH14-related_disorder": 26,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified": 11,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|MYH14-related_disorder|not_provided": 1,
    "MYH14-related_disorder|not_provided|not_specified": 3,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 11,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 15,
    "MYH14-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_provided": 6,
    "MYH14-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_provided": 24,
    "MYH14-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_provided|not_specified": 7,
    "not_provided|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 2,
    "Meniere_disease|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "MYH14-related_disorder|Nonsyndromic_Hearing_Loss|_Dominant": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified|not_provided": 7,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 6,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 5,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 3,
    "not_provided|MYH14-related_disorder": 8,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 17,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified|not_provided": 2,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 5,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified|not_provided|MYH14-related_disorder": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|MYH14-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_provided|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified": 3,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|MYH14-related_disorder": 1,
    "not_specified|not_provided|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MYH14-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Inborn_genetic_diseases|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|not_specified": 1,
    "MYH14-related_disorder|not_provided": 8,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 6,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_provided": 2,
    "MYH14-related_disorder|not_specified|not_provided": 2,
    "Sensorineural_hearing_loss_disorder|Peripheral_neuropathy|EMG_abnormality|Peripheral_axonal_neuropathy|EMG:_axonal_abnormality|Motor_polyneuropathy|Impaired_vibration_sensation_in_the_lower_limbs|Progressive_sensorineural_hearing_impairment": 1,
    "MYH14-related_disorder|not_specified": 3,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A|MYH14-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_specified": 1,
    "not_specified|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "MYH14-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|not_specified": 1,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 2,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Hearing_impairment": 1,
    "not_provided|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 3,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 4,
    "Inborn_genetic_diseases|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "not_provided|not_specified|Meniere_disease|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Inborn_genetic_diseases|not_provided": 2,
    "Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 2,
    "MYH14-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|MYH14-related_disorder|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_provided|Hearing_impairment|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "not_provided|not_specified|MYH14-related_disorder": 1,
    "not_specified|not_provided|MYH14-related_disorder|Inborn_genetic_diseases": 1,
    "Hearing_impairment|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "Inborn_genetic_diseases|MYH14-related_disorder": 1,
    "not_provided|not_specified|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|MYH14-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified": 2,
    "not_provided|MYH14-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A|not_specified|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "MYH14-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|MYH14-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_4A": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_4A|Peripheral_neuropathy-myopathy-hoarseness-hearing_loss_syndrome": 1,
    "Spinocerebellar_ataxia_type_13|not_provided": 7,
    "Spinocerebellar_ataxia_type_13": 20,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_13|not_specified": 1,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_13": 2,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_13|not_provided": 2,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_13|KCNC3-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|KCNC3-related_disorder|Spinocerebellar_ataxia_type_13": 1,
    "Tip-toe_gait|not_provided|Spinocerebellar_ataxia_type_13": 1,
    "not_provided|Inborn_genetic_diseases|KCNC3-related_disorder": 1,
    "Spinocerebellar_ataxia_type_13|not_provided|not_specified": 2,
    "KCNC3-related_disorder|not_specified|not_provided": 1,
    "not_provided|KCNC3-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_13": 1,
    "Hereditary_ataxia|not_provided|Spinocerebellar_ataxia_type_13": 1,
    "not_provided|Spinocerebellar_ataxia_type_13": 3,
    "not_specified|KCNC3-related_disorder|not_provided": 1,
    "KCNC3-related_disorder": 1,
    "KCNC3-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Cleft_palate": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_13": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_13": 1,
    "KCNC3-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified": 3,
    "Colorectal_cancer|_susceptibility_to|_10": 2128,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 572,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 662,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided": 57,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified": 50,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 4,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer": 1,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 51,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified": 11,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 54,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 105,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided|Endometrial_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided": 45,
    "Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 7,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 9,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 7,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10": 20,
    "Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 3,
    "Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10": 3,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 1,
    "not_provided|Hereditary_cancer|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10": 41,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|not_specified": 3,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified": 1,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "POLD1-related_disorder|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10": 11,
    "POLD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 18,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 2,
    "not_provided|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified": 27,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|not_specified": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided": 7,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "Colorectal_cancer|_susceptibility_to|_10|Adenomatous_polyp_of_colon|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon": 2,
    "POLD1-related_disorder|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 4,
    "not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 3,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 4,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "POLD1-related_disorder|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided|Colon_cancer": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 3,
    "POLD1-related_disorder|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLD1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome": 13,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 2,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_colorectal_cancer|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Familial_colorectal_cancer": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 2,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome": 5,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 4,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 1,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLD1-related_disorder|not_specified|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "POLD1-related_disorder": 7,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Malignant_tumor_of_breast|See_cases|not_specified|not_provided": 1,
    "Familial_colorectal_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 3,
    "not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10": 2,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 3,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 5,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Endometrial_carcinoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 3,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided": 3,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10": 5,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 2,
    "not_specified|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided": 1,
    "Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLD1-related_disorder|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified": 3,
    "not_specified|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon": 2,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 4,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|POLD1-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Familial_colorectal_cancer|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided|Immunodeficiency_120": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided|Carcinoma_of_colon|Familial_colorectal_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|not_provided": 1,
    "POLD1-related_disorder|not_specified|Colorectal_cancer|_susceptibility_to|_10": 3,
    "Familial_colorectal_cancer_type_X|not_specified|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "POLD1-related_disorder|Bile_duct_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|not_provided": 2,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 3,
    "Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 2,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Familial_colorectal_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_specified|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 2,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|not_provided": 1,
    "not_specified|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome": 2,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|POLD1-related_disorder|Malignant_tumor_of_breast|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_provided|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10": 1,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|POLD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 1,
    "POLD1-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided": 4,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 2,
    "Familial_colorectal_cancer|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10": 2,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|not_specified": 1,
    "POLD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 2,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Familial_colorectal_cancer_type_X|not_specified|not_provided": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|not_specified|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 4,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 1,
    "Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|_10|not_specified|not_provided": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120": 2,
    "POLD1-related_disorder|not_provided|not_specified": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|POLD1-related_disorder|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10": 3,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome": 2,
    "not_specified|Carcinoma_of_colon|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Malignant_tumor_of_breast": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided|POLD1-related_disorder": 1,
    "not_provided|POLD1-related_disorder|not_specified|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120": 2,
    "Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis|not_provided": 1,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 6,
    "Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 4,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Carcinoma_of_colon": 1,
    "Carcinoma_of_colon|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis|not_specified|not_provided": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10|Malignant_tumor_of_breast": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "POLD1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Hereditary_cancer-predisposing_syndrome": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|POLD1-related_disorder": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer_type_X": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Familial_colorectal_cancer|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 2,
    "POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Familial_colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|POLD1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|POLD1-related_disorder|not_provided": 1,
    "POLD1-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|not_provided": 2,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Immunodeficiency_120|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_colorectal_cancer_type_X|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10|not_specified|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120": 1,
    "not_provided|POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified": 1,
    "not_specified|POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided|POLD1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "not_specified|Carcinoma_of_colon": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|POLD1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "not_specified|Carcinoma_of_colon|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "POLD1-related_disorder|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|not_provided": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10": 2,
    "not_specified|Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Hereditary_cancer-predisposing_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|not_provided|Familial_colorectal_cancer": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Endometrial_carcinoma|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 1,
    "not_specified|Colorectal_cancer|_susceptibility_to|_10|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Polymerase_proofreading-related_adenomatous_polyposis": 1,
    "Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Colorectal_cancer|Colorectal_cancer|_susceptibility_to|_10": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Carcinoma_of_colon|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Colorectal_cancer|_susceptibility_to|_10|POLD1-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis|not_specified|not_provided": 1,
    "not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_specified|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|Carcinoma_of_colon": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|Familial_colorectal_cancer|not_provided|POLD1-related_disorder": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120": 1,
    "Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Mandibular_hypoplasia-deafness-progeroid_syndrome|Micrognathia": 1,
    "not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_specified|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "not_provided|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_specified|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Colorectal_cancer|_susceptibility_to|_10|not_specified|Carcinoma_of_colon|not_provided": 1,
    "Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_colorectal_cancer_type_X": 1,
    "not_specified|not_provided|POLD1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Immunodeficiency_120": 1,
    "Combined_immunodeficiency|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|Polymerase_proofreading-related_adenomatous_polyposis|Familial_colorectal_cancer_type_X|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|Hereditary_cancer|Colorectal_cancer|_susceptibility_to|_10|not_provided|Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome": 1,
    "POLD1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|_susceptibility_to|_10|not_provided|Mandibular_hypoplasia-deafness-progeroid_syndrome|Immunodeficiency_120|Familial_colorectal_cancer_type_X|Polymerase_proofreading-related_adenomatous_polyposis|not_specified": 1,
    "not_provided|Polymerase_proofreading-related_adenomatous_polyposis|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_colorectal_cancer|Colorectal_cancer|_susceptibility_to|_10|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|POLD1-related_disorder|not_provided|Colorectal_cancer|_susceptibility_to|_10": 1,
    "Immunodeficiency_120|Mandibular_hypoplasia-deafness-progeroid_syndrome|Colorectal_cancer|_susceptibility_to|_10|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Mandibular_hypoplasia-deafness-progeroid_syndrome|not_provided": 1,
    "MYBPC2-related_disorder": 7,
    "not_provided|MYBPC2-related_disorder": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_variable_seizures": 7,
    "EMC10-related_disorder|Neurodevelopmental_disorder_with_dysmorphic_facies_and_variable_seizures": 2,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_variable_seizures|Intellectual_disability": 1,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_variable_seizures|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Neurodevelopmental_disorder_with_dysmorphic_facies_and_variable_seizures": 1,
    "SHANK1-related_disorder": 38,
    "not_provided|SHANK1-related_disorder": 4,
    "SHANK1-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|SHANK1-related_disorder": 3,
    "SHANK1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "SHANK1-associated_disorder|not_provided": 1,
    "Inborn_genetic_diseases|EBV-positive_nodal_T-_and_NK-cell_lymphoma|SHANK1-associated_neurodevelopmental_disorder": 1,
    "SHANK1-related_Neurodevelopmental_Disorder|See_cases": 1,
    "SHANK1-related_Neurodevelopmental_Disorder": 1,
    "SHANK1-related_autism": 1,
    "ACP4-related_disorder": 13,
    "Amelogenesis_imperfecta|_type_1J": 9,
    "Amelogenesis_imperfecta|_type_1J|not_provided": 1,
    "Amelogenesis_imperfecta|not_specified": 1,
    "ACP4-related_disorder|not_provided": 1,
    "Amelogenesis_imperfecta|_type_1J|Amelogenesis_imperfecta|Amelogenesis_imperfecta_type_1": 1,
    "Kallikrein|_decreased_urinary_activity_of": 1,
    "KLK3-related_disorder": 15,
    "not_provided|KLK4-related_disorder": 1,
    "Inborn_genetic_diseases|KLK4-related_disorder": 1,
    "Male_infertility|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Amelogenesis_imperfecta_type_2A1": 2,
    "Amelogenesis_imperfecta_type_2A1": 4,
    "KLK4-related_disorder": 1,
    "not_provided|Ichthyosis_with_erythrokeratoderma": 1,
    "Ichthyosis_with_erythrokeratoderma": 1,
    "CD33-related_disorder": 2,
    "not_provided|CD33-related_disorder": 2,
    "CD33-related_disorder|not_provided": 1,
    "ETFB-related_disorder|Multiple_acyl-CoA_dehydrogenase_deficiency": 2,
    "Glutaric_acidemia_IIb": 1,
    "not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|ETFB-related_disorder": 1,
    "ETFB-related_disorder|Inborn_genetic_diseases|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Glutaric_acidemia_IIb|Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|not_provided|not_specified": 2,
    "not_specified|Glutaric_acidemia_IIb|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "ETFB-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency|Chronic_kidney_disease": 1,
    "Glutaric_acidemia_IIc|Multiple_acyl-CoA_dehydrogenase_deficiency|not_specified": 1,
    "Multiple_acyl-CoA_dehydrogenase_deficiency|ETFB-related_disorder": 2,
    "ETFB-related_disorder": 4,
    "ETFB-related_disorder|not_specified|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 2,
    "ETFB-related_disorder|not_provided|Multiple_acyl-CoA_dehydrogenase_deficiency": 1,
    "Cortical_pulverulent_cataract|not_provided": 1,
    "Cataract_19_multiple_types": 36,
    "Inborn_genetic_diseases|Cataract_19_multiple_types": 9,
    "Cataract_19_multiple_types|Inborn_genetic_diseases": 7,
    "LIM2-related_disorder": 3,
    "not_provided|Cataract|Cataract_19_multiple_types|LIM2-related_disorder": 1,
    "Cataract_19_multiple_types|not_provided": 4,
    "not_provided|Cataract_19_multiple_types": 1,
    "not_provided|Inborn_genetic_diseases|Cataract_19_multiple_types": 1,
    "Cataract_19_multiple_types|LIM2-related_disorder": 2,
    "Inborn_genetic_diseases|LIM2-related_disorder": 1,
    "Cataract_19_multiple_types|LIM2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Gingival_disorder": 183,
    "FPR1-related_disorder": 1,
    "not_provided|not_specified|Gingival_disorder": 1,
    "Gingival_disorder|not_specified": 9,
    "not_provided|Gingival_disorder|not_specified": 3,
    "not_specified|Gingival_disorder": 5,
    "Gingival_disorder|FPR1-related_disorder": 3,
    "not_provided|FPR1-related_disorder|Gingival_disorder": 2,
    "not_provided|Gingival_disorder": 3,
    "FPR1-related_disorder|Gingival_disorder": 1,
    "Periodontitis": 2,
    "Gingival_disorder|not_provided": 6,
    "not_specified|Gingival_disorder|not_provided": 2,
    "Gingival_disorder|not_provided|FPR1_POLYMORPHISM": 1,
    "Gingival_disorder|FPR1-related_disorder|not_specified|not_provided": 1,
    "FPR1-related_disorder|not_provided|Gingival_disorder": 2,
    "Gingival_disorder|not_provided|not_specified": 1,
    "Houge-Janssens_syndrome_2": 19,
    "not_specified|not_provided|Houge-Janssens_syndrome_2": 1,
    "PPP2R1A-related_disorder|not_provided": 8,
    "Houge-Janssens_syndrome_2|not_provided": 7,
    "not_provided|Houge-Janssens_syndrome_2": 6,
    "Houge-Janssens_syndrome_2|not_provided|PPP2R1A-related_neurodevelopmental_disorders|PPP2R1A-related_disorder|Inborn_genetic_diseases": 1,
    "PPP2R1A-related_disorder|not_provided|Houge-Janssens_syndrome_2": 1,
    "Inborn_genetic_diseases|Houge-Janssens_syndrome_2|not_provided": 1,
    "Houge-Janssens_syndrome_2|not_provided|Intellectual_disability": 1,
    "not_provided|not_specified|Houge-Janssens_syndrome_2|See_cases": 1,
    "Inborn_genetic_diseases|Houge-Janssens_syndrome_2|PPP2R1A-related_disorder|not_provided": 1,
    "PPP2R1A-related_disorder": 1,
    "not_provided|PPP2R1A-related_disorder": 2,
    "Hypercalcemia|_infantile|_1": 135,
    "Pancreatic_agenesis_3": 6,
    "See_cases|Pancreatic_agenesis_3": 1,
    "Familial_cold_autoinflammatory_syndrome": 3,
    "Familial_cold_autoinflammatory_syndrome_2|not_provided": 30,
    "not_provided|Familial_cold_autoinflammatory_syndrome_2": 40,
    "NLRP12-related_disorder": 5,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2": 27,
    "Inborn_genetic_diseases|NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Inborn_genetic_diseases": 35,
    "NLRP12-related_disorder|not_provided|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome": 1,
    "Multisystem_inflammatory_syndrome_in_children|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|not_provided|NLRP12-related_disorder": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|not_provided": 9,
    "not_provided|NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome": 1,
    "NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2": 25,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome": 13,
    "Familial_cold_autoinflammatory_syndrome_2|not_specified": 4,
    "NLRP12-related_disorder|not_specified|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome|not_provided": 1,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2|not_provided": 4,
    "Inborn_genetic_diseases|Autoinflammatory_syndrome|not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Multisystem_inflammatory_syndrome_in_children|not_specified|Familial_cold_autoinflammatory_syndrome_2|Familial_cold_autoinflammatory_syndrome|not_provided|NLRP12-related_disorder": 1,
    "Autoinflammatory_syndrome|NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "NLRP12-related_disorder|Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome": 8,
    "Autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2": 10,
    "Autoinflammatory_syndrome|NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|not_provided": 1,
    "NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_2": 2,
    "not_provided|NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2": 2,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2|not_provided": 2,
    "not_provided|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|Inborn_genetic_diseases|not_specified|NLRP12-related_disorder": 1,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2|not_provided|Autoinflammatory_syndrome|NLRP12-related_disorder": 1,
    "Familial_cold_autoinflammatory_syndrome_2|NLRP12-related_disorder": 8,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome": 1,
    "Familial_cold_autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2|not_specified": 1,
    "Familial_cold_autoinflammatory_syndrome|not_specified|Autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "not_provided|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2": 2,
    "Familial_cold_autoinflammatory_syndrome_2|not_specified|not_provided": 1,
    "Familial_cold_autoinflammatory_syndrome_2|NLRP12-related_disorder|Autoinflammatory_syndrome": 1,
    "not_provided|Familial_cold_autoinflammatory_syndrome_2|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2|NLRP12-related_disorder": 1,
    "not_provided|NLRP12-related_disorder": 1,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Inborn_genetic_diseases|not_provided": 3,
    "Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|not_specified|Autoinflammatory_syndrome": 1,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2|not_provided": 3,
    "not_specified|Familial_cold_autoinflammatory_syndrome_2": 2,
    "Familial_cold_autoinflammatory_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2|not_provided|NLRP12-related_disorder": 1,
    "NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|See_cases": 1,
    "Inborn_genetic_diseases|NLRP12-related_disorder|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|Inborn_genetic_diseases": 1,
    "Autoinflammatory_syndrome|Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|NLRP12-related_disorder|not_provided": 1,
    "NLRP12-related_disorder|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome_2|not_provided|NLRP12-related_disorder": 1,
    "Familial_cold_autoinflammatory_syndrome|FAMILIAL_COLD_AUTOINFLAMMATORY_SYNDROME_2|_SUSCEPTIBILITY_TO|Autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2|not_specified": 1,
    "NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2": 5,
    "Familial_cold_autoinflammatory_syndrome_2|not_provided|not_specified": 1,
    "Familial_cold_autoinflammatory_syndrome_2|See_cases": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Inborn_genetic_diseases|NLRP12-related_disorder": 1,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2|not_specified|not_provided": 1,
    "NLRP12-associated_autoinflammatory_disease": 1,
    "Periodic_fever_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|not_provided|not_specified": 1,
    "not_provided|Autoinflammatory_syndrome|Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome|not_specified|Familial_cold_autoinflammatory_syndrome_2|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|Familial_cold_autoinflammatory_syndrome_2|not_provided": 1,
    "Autoinflammatory_syndrome|not_specified|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Autoimmune_interstitial_lung_disease-arthritis_syndrome|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Childhood-onset_schizophrenia|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Autoinflammatory_syndrome|NLRP12-related_disorder|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "not_provided|Autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2|NLRP12-related_disorder": 1,
    "Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|NLRP12-related_disorder": 1,
    "Autoinflammatory_syndrome|not_provided|not_specified|Familial_cold_autoinflammatory_syndrome_2": 1,
    "NLRP12-related_disorder|Familial_cold_autoinflammatory_syndrome_2|Inborn_genetic_diseases|Autoinflammatory_syndrome|not_provided": 1,
    "not_specified|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "not_specified|Familial_cold_autoinflammatory_syndrome|not_provided|Familial_cold_autoinflammatory_syndrome_2": 1,
    "not_specified|Familial_cold_autoinflammatory_syndrome_2|NLRP12-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Familial_cold_autoinflammatory_syndrome_2|Autoinflammatory_syndrome|NLRP12-related_disorder": 1,
    "not_specified|not_provided|Familial_cold_autoinflammatory_syndrome|Familial_cold_autoinflammatory_syndrome_2": 1,
    "Familial_cold_autoinflammatory_syndrome|not_specified|not_provided": 1,
    "Spinocerebellar_ataxia_type_14": 70,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_14": 2,
    "Spinocerebellar_ataxia_type_14|not_provided": 23,
    "PRKCG-related_disorder": 6,
    "not_provided|Spinocerebellar_ataxia_type_14": 11,
    "not_specified|Spinocerebellar_ataxia_type_14|not_provided": 3,
    "Autosomal_dominant_cerebellar_ataxia|Spinocerebellar_ataxia_type_14": 1,
    "not_provided|PRKCG-related_disorder": 2,
    "Cerebellar_ataxia|not_specified": 1,
    "Spinocerebellar_ataxia_type_14|PRKCG-related_disorder": 1,
    "PRKCG-related_disorder|not_provided|Spinocerebellar_ataxia_type_14": 1,
    "not_provided|Spinocerebellar_ataxia_type_14|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_cerebellar_ataxia": 1,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_14": 1,
    "not_provided|not_specified|PRKCG-related_disorder|Spinocerebellar_ataxia_type_14": 1,
    "PRKCG-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_14": 1,
    "PRKCG-related_disorder|Spinocerebellar_ataxia_type_14": 1,
    "Spinocerebellar_ataxia_type_14|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_type_14|Inborn_genetic_diseases": 1,
    "PRPF31-related_disorder": 3,
    "PRPF31-related_disorder|not_provided": 6,
    "not_provided|Retinitis_pigmentosa|PRPF31-related_disorder|Retinal_dystrophy": 1,
    "not_provided|PRPF31-related_disorder": 5,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa_11": 2,
    "Retinitis_pigmentosa_11|Retinal_dystrophy|not_provided": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_11": 2,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_11": 4,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_11": 2,
    "PRPF31-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_11": 2,
    "Retinitis_pigmentosa|PRPF31-related_disorder|not_provided|Retinitis_pigmentosa_11": 1,
    "Retinitis_pigmentosa_11|not_provided": 4,
    "Retinitis_pigmentosa_11|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|See_cases": 1,
    "not_provided|Retinitis_pigmentosa_11|Retinitis_pigmentosa|not_specified": 1,
    "not_provided|Retinitis_pigmentosa_11|Retinal_dystrophy": 2,
    "Inborn_genetic_diseases|Retinitis_pigmentosa_11|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_11": 6,
    "not_provided|Retinitis_pigmentosa|PRPF31-related_disorder": 1,
    "Retinitis_pigmentosa|not_provided|PRPF31-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|PRPF31-related_disorder": 1,
    "not_provided|PRPF31-related_disorder|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|not_provided|Retinal_dystrophy|Retinitis_pigmentosa_11": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa|PRPF31-related_disorder|Retinitis_pigmentosa_11|not_provided": 1,
    "PRPF31-related_disorder|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "Early-onset_retinitis_pigmentosa|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_11|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_11|Retinitis_pigmentosa|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_11|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa|Retinal_dystrophy|Retinitis_pigmentosa_11": 2,
    "not_provided|PRPF31-related_disorder|Retinitis_pigmentosa_11": 1,
    "Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies": 73,
    "CNOT3-related_disorder": 17,
    "Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies|not_provided": 7,
    "CNOT3-related_disorder|not_provided": 10,
    "Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies|Inborn_genetic_diseases|CNOT3-related_disorder": 1,
    "not_provided|Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Moyamoya_angiopathy_with_developmental_delay|Complex_neurodevelopmental_disorder": 1,
    "CNOT3-related_disorder|Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies|not_provided": 1,
    "CNOT3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|CNOT3-related_disorder|not_provided": 1,
    "not_provided|CNOT3-related_disorder|Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies": 1,
    "not_provided|CNOT3-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies": 1,
    "Intellectual_developmental_disorder_with_speech_delay|_autism|_and_dysmorphic_facies|CNOT3-associated_disorder": 1,
    "TMC4-related_disorder": 5,
    "Intellectual_disability|_autosomal_recessive_57|not_specified": 1,
    "Intellectual_disability|_autosomal_recessive_57|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_autosomal_recessive_57": 25,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_recessive_57": 2,
    "Neurodevelopmental_abnormality|Intellectual_disability|_autosomal_recessive_57": 1,
    "Intellectual_disability|_autosomal_recessive_57|not_provided": 6,
    "not_provided|Inborn_genetic_diseases|MBOAT7-related_disorder": 1,
    "MBOAT7-related_disorder": 7,
    "MBOAT7-related_disorder|not_provided": 2,
    "not_provided|Intellectual_disability|_autosomal_recessive_57": 1,
    "Intellectual_disability|_autosomal_recessive_57|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MBOAT7-related_disorder": 1,
    "Intellectual_disability|_autosomal_recessive_57|not_provided|Intellectual_disability": 1,
    "Intellectual_disability|_autosomal_recessive_57|MBOAT7-related_disorder": 1,
    "Pontocerebellar_hypoplasia_type_2C": 3,
    "not_provided|TSEN34-related_disorder": 1,
    "Pontoneocerebellar_hypoplasia|not_specified|not_provided|Pontocerebellar_hypoplasia_type_2C": 1,
    "Pontocerebellar_hypoplasia_type_2C|not_provided": 1,
    "TSEN34-related_disorder": 2,
    "not_specified|not_provided|TSEN34-related_disorder|Pontoneocerebellar_hypoplasia": 1,
    "RPS9-related_disorder": 2,
    "LENG8-related_disorder": 14,
    "not_provided|LENG8-related_disorder": 1,
    "KIR2DL1-related_disorder": 8,
    "not_provided|KIR2DL1-related_disorder": 1,
    "Hydatidiform_mole|_recurrent|_1": 157,
    "Hydatidiform_mole|_recurrent|_1|not_provided": 10,
    "not_provided|Inborn_genetic_diseases|Hydatidiform_mole|_recurrent|_1": 1,
    "not_provided|Hydatidiform_mole": 2,
    "Hydatidiform_mole|not_provided|Hydatidiform_mole|_recurrent|_1": 2,
    "NLRP7-related_disorder": 4,
    "not_provided|Hydatidiform_mole|_recurrent|_1": 20,
    "not_specified|Hydatidiform_mole|_recurrent|_1|not_provided": 1,
    "Inborn_genetic_diseases|Hydatidiform_mole|_recurrent|_1": 2,
    "not_provided|Hydatidiform_mole|Hydatidiform_mole|_recurrent|_1": 1,
    "Hydatidiform_mole|not_specified|Hydatidiform_mole|_recurrent|_1|not_provided": 1,
    "not_provided|NLRP7-related_disorder": 1,
    "NLRP7-related_disorder|Hydatidiform_mole|_recurrent|_1": 1,
    "not_specified|not_provided|Hydatidiform_mole|_recurrent|_1": 2,
    "NLRP7-related_disorder|not_provided|Hydatidiform_mole|_recurrent|_1|Inborn_genetic_diseases": 1,
    "Hydatidiform_mole|Hydatidiform_mole|_recurrent|_1|not_provided": 1,
    "Hydatidiform_mole|_recurrent|_1|not_specified|not_provided": 1,
    "not_specified|not_provided|Hydatidiform_mole|_recurrent|_1|NLRP7-related_disorder": 1,
    "not_provided|Hydatidiform_mole|_recurrent|_1|not_specified": 1,
    "Hydatidiform_mole|_recurrent|_1|Inborn_genetic_diseases": 6,
    "not_provided|NLRP7-related_disorder|Hydatidiform_mole|_recurrent|_1": 1,
    "not_provided|Hydatidiform_mole|_recurrent|_1|Prostate_cancer": 1,
    "Hydatidiform_mole|_recurrent|_1|not_provided|not_specified": 2,
    "not_provided|not_specified|Hydatidiform_mole|_recurrent|_1": 1,
    "Hydatidiform_mole|Hydatidiform_mole|_recurrent|_1": 1,
    "Hydatidiform_mole|_recurrent|_1|NLRP7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "NLRP2-related_disorder|not_provided": 18,
    "NLRP2-related_disorder": 58,
    "not_provided|NLRP2-related_disorder": 16,
    "Oocyte/zygote/embryo_maturation_arrest_18": 4,
    "Oocyte/zygote/embryo_maturation_arrest_18|not_provided": 1,
    "not_provided|Platelet-type_bleeding_disorder_11|not_specified": 5,
    "not_provided|GP6-related_disorder": 4,
    "GP6-related_disorder|not_provided": 2,
    "not_specified|Platelet-type_bleeding_disorder_11|not_provided": 1,
    "GP6-related_disorder": 2,
    "not_provided|not_specified|GP6-related_disorder": 1,
    "Platelet-type_bleeding_disorder_11": 5,
    "not_specified|not_provided|Platelet-type_bleeding_disorder_11": 2,
    "GP6-related_disorder|not_specified|not_provided": 1,
    "GP6-related_disorder|Platelet-type_bleeding_disorder_11|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|GP6-related_disorder": 1,
    "Platelet-type_bleeding_disorder_11|not_provided": 1,
    "not_provided|not_specified|Platelet-type_bleeding_disorder_11": 2,
    "Platelet-type_bleeding_disorder_11|not_specified|not_provided": 1,
    "Platelet-type_bleeding_disorder_11|not_specified": 1,
    "not_specified|GP6-related_disorder|not_provided": 1,
    "not_specified|not_provided|Platelet-type_bleeding_disorder_11|Thrombocytopenia|Abnormal_bleeding": 1,
    "GP6-related_disorder|not_provided|not_specified": 1,
    "Nemaline_myopathy_5": 232,
    "not_provided|not_specified|Nemaline_myopathy_5": 2,
    "not_provided|Nemaline_myopathy_5": 14,
    "Nemaline_myopathy_5|not_provided": 9,
    "not_specified|Nemaline_myopathy_5|not_provided": 2,
    "Nemaline_myopathy_5|Nemaline_myopathy_5C|_autosomal_dominant": 1,
    "Nemaline_myopathy_5B|_autosomal_recessive|_childhood-onset": 3,
    "Inborn_genetic_diseases|Nemaline_myopathy_5": 3,
    "Nemaline_myopathy_5|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|TNNT1-related_disorder|Nemaline_myopathy_5": 1,
    "not_specified|Nemaline_myopathy_5": 3,
    "not_provided|Inborn_genetic_diseases|Nemaline_myopathy_5": 2,
    "Inborn_genetic_diseases|Nemaline_myopathy_5|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Nemaline_myopathy_5": 2,
    "Nemaline_myopathy_5|Nemaline_Myopathy|_Recessive|not_provided": 1,
    "Nemaline_myopathy_5C|_autosomal_dominant|Nemaline_myopathy_5": 1,
    "Nemaline_myopathy_5|not_specified": 3,
    "TNNT1-related_disorder|Nemaline_myopathy_5B|_autosomal_recessive|_childhood-onset": 1,
    "Nemaline_myopathy_5|Nemaline_myopathy_5B|_autosomal_recessive|_childhood-onset": 1,
    "Nemaline_myopathy_5C|_autosomal_dominant": 1,
    "not_provided|Nemaline_myopathy_5|TNNT1-related_disorder": 1,
    "TNNT1-related_disorder|Nemaline_myopathy_5": 1,
    "Inborn_genetic_diseases|Nemaline_myopathy_5|not_specified": 1,
    "Nemaline_myopathy_5|not_provided|not_specified": 1,
    "not_specified|not_provided|Nemaline_myopathy_5": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Nemaline_myopathy_5|Hypertrophic_cardiomyopathy": 1,
    "Nemaline_myopathy_5|Nemaline_myopathy_5C|_autosomal_dominant|Nemaline_myopathy_5B|_autosomal_recessive|_childhood-onset": 1,
    "not_provided|Familial_restrictive_cardiomyopathy|Nemaline_myopathy_5|Hypertrophic_cardiomyopathy|not_specified|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Nemaline_Myopathy|_Recessive": 1,
    "TNNT1-related_disorder": 1,
    "Nemaline_Myopathy|_Recessive|not_specified": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Nemaline_Myopathy|_Recessive|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Nemaline_myopathy_5|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7": 1,
    "not_provided|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7": 1,
    "Cardiomyopathy|_familial_restrictive|_1": 5,
    "not_provided|Familial_restrictive_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_7": 9,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|TNNI3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_7": 1,
    "TNNI3-associated_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_7": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 2,
    "Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Restrictive_cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|SUDDEN_INFANT_DEATH_SYNDROME|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|not_provided|Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7": 2,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME|not_provided|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome": 1,
    "not_provided|TNNI3-related_disorder": 1,
    "not_provided|Cardiomyopathy|Dilated_cardiomyopathy_1FF|Primary_dilated_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "TNNI3-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype|not_specified|Primary_ciliary_dyskinesia|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|_familial_restrictive|_1|not_specified": 1,
    "Hypertrophic_cardiomyopathy|Restrictive_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_1": 1,
    "Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiomyopathy|Sudden_cardiac_arrest|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "TNNI3-related_disorder|Cardiovascular_phenotype|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|TNNI3-related_disorder|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "TNNI3-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7": 2,
    "Dilated_cardiomyopathy_2A": 3,
    "not_provided|Hypertrophic_cardiomyopathy_7": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Dilated_cardiomyopathy_2A|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|not_provided|Cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Restrictive_cardiomyopathy|TNNI3-related_disorder|Dilated_cardiomyopathy_1FF|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|not_provided|Cardiomyopathy|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_7|not_provided|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Cardiomyopathy|Hypertrophic_cardiomyopathy_7": 1,
    "TNNI3-related_disorder|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy|_familial_restrictive|_1": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|not_specified|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Nemaline_Myopathy|_Recessive|not_specified|Primary_ciliary_dyskinesia|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|not_provided|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_cardiomyopathy_2A|not_specified|Cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Dilated_cardiomyopathy_1FF|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|not_specified|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|TNNI3-related_disorder|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7": 1,
    "not_provided|Long_QT_syndrome|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|not_specified": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1FF|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|Dilated_cardiomyopathy_1FF": 1,
    "Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_1FF|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A": 1,
    "Hypertrophic_cardiomyopathy|TNNI3-related_disorder": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|not_provided|Cardiovascular_phenotype|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_7|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Amyloidosis|_hereditary_systemic_1|Cardiomyopathy|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Familial_restrictive_cardiomyopathy|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_7|not_specified|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1FF|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy|not_provided|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_7": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Myocarditis|Primary_familial_dilated_cardiomyopathy|not_specified|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype|not_specified|not_provided|Primary_ciliary_dyskinesia|Cardiomyopathy|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|not_specified|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype|Familial_restrictive_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_2A|Dilated_cardiomyopathy_1FF": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Cardiovascular_phenotype": 1,
    "Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_1|not_specified|not_provided|Hypertrophic_cardiomyopathy|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7": 1,
    "TNNI3-related_disorder": 1,
    "Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Primary_ciliary_dyskinesia|Cardiomyopathy|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_2A|not_provided|Cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7": 1,
    "not_provided|TNNI3-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_1FF|not_provided": 1,
    "Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|not_specified|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_1FF|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy": 1,
    "Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_1FF|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Cardiomyopathy": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_7|Dilated_cardiomyopathy_1FF|Dilated_cardiomyopathy_2A|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_1A|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_7": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|TNNI3-related_disorder|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Primary_ciliary_dyskinesia|Cardiomyopathy|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Primary_ciliary_dyskinesia|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Hypertrophic_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_1FF|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A": 1,
    "not_provided|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|not_provided": 1,
    "Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy|not_provided": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Hypertrophic_cardiomyopathy|Familial_restrictive_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Familial_restrictive_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome": 1,
    "Primary_ciliary_dyskinesia_2|Primary_ciliary_dyskinesia|DNAAF3-related_disorder|not_provided": 1,
    "DNAAF3-related_disorder|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_2": 1,
    "DDX41-related_hematologic_malignancy_predisposition_syndrome|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia_2|Primary_ciliary_dyskinesia|Hypertrophic_cardiomyopathy|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Familial_restrictive_cardiomyopathy": 1,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_2": 2,
    "not_specified|Primary_ciliary_dyskinesia|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A": 1,
    "Primary_ciliary_dyskinesia_2|not_provided|not_specified|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_2": 7,
    "Primary_ciliary_dyskinesia|Familial_restrictive_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome": 1,
    "DNAAF3-related_disorder|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_2": 1,
    "Primary_ciliary_dyskinesia|DNAAF3-related_disorder": 4,
    "Primary_ciliary_dyskinesia_2|not_specified|not_provided|Hypertrophic_cardiomyopathy|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Dilated_Cardiomyopathy|_Recessive|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia": 1,
    "Familial_restrictive_cardiomyopathy|not_provided|Primary_ciliary_dyskinesia|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_specified|Primary_ciliary_dyskinesia_2": 1,
    "Primary_ciliary_dyskinesia_2|not_provided|Primary_ciliary_dyskinesia|DNAAF3-related_disorder": 1,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy": 2,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Primary_ciliary_dyskinesia|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1|Dilated_cardiomyopathy_2A": 1,
    "Primary_ciliary_dyskinesia|DNAAF3-related_disorder|Primary_ciliary_dyskinesia_2": 1,
    "Primary_ciliary_dyskinesia_2|Primary_ciliary_dyskinesia": 8,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_2": 1,
    "DNAAF3-related_disorder|Primary_ciliary_dyskinesia|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia_2": 1,
    "DNAAF3-related_disorder|not_provided|Primary_ciliary_dyskinesia": 3,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia_2": 1,
    "Primary_ciliary_dyskinesia_2|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_specified|Primary_ciliary_dyskinesia|not_provided|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia_2": 1,
    "DNAAF3-related_disorder|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|not_provided|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia|Hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Familial_restrictive_cardiomyopathy|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|Dilated_Cardiomyopathy|_Recessive|Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Familial_restrictive_cardiomyopathy|Primary_ciliary_dyskinesia": 1,
    "Familial_Hypertrophic_Cardiomyopathy_with_Wolff-Parkinson-White_Syndrome|Primary_ciliary_dyskinesia|Dilated_cardiomyopathy_2A|Hypertrophic_cardiomyopathy_7|Cardiomyopathy|_familial_restrictive|_1": 1,
    "DNAAF3-related_disorder|Primary_ciliary_dyskinesia": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_2": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_2": 1,
    "PTPRH-related_disorder": 1,
    "SSC5D-related_disorder": 1,
    "ZNF865-related_disorder": 1,
    "Developmental_delay|_dysmorphic_facies|_and_brain_anomalies|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Developmental_delay|_dysmorphic_facies|_and_brain_anomalies": 1,
    "Developmental_delay|_dysmorphic_facies|_and_brain_anomalies": 3,
    "NLRP5-related_disorder": 28,
    "Oocyte/zygote/embryo_maturation_arrest_19": 7,
    "NLRP5-related_disorder|not_provided": 7,
    "not_provided|NLRP5-related_disorder": 8,
    "Inherited_oocyte_maturation_defect|Oocyte/zygote/embryo_maturation_arrest_19": 2,
    "not_specified|NLRP5-related_disorder|not_provided": 1,
    "Preimplantation_lethality": 1,
    "Toriello-Lacassie-Droste_syndrome|not_provided": 1,
    "ZNF582-related_disorder": 3,
    "PEG3-related_disorder": 3,
    "not_provided|PEG3-related_disorder": 2,
    "PEG3-related_disorder|not_provided": 1,
    "ZNF264-related_disorder": 1,
    "Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA|not_provided": 4,
    "Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA": 17,
    "not_provided|not_specified|Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA": 1,
    "not_provided|Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA": 2,
    "Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA|AURKC-related_disorder": 1,
    "not_provided|Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA|AURKC-related_disorder": 1,
    "AURKC-related_disorder|not_provided|Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA": 1,
    "Infertility_associated_with_multi-tailed_spermatozoa_and_excessive_DNA|Male_infertility_with_spermatogenesis_disorder": 1,
    "ZNF17-related_disorder": 2,
    "not_provided|ZNF17-related_disorder": 1,
    "not_specified|ZNF17-related_disorder": 1,
    "SLC27A5-related_disorder": 37,
    "SLC27A5-related_disorder|not_provided": 20,
    "not_specified|SLC27A5-related_disorder": 2,
    "SLC27A5-related_disorder|not_specified": 2,
    "not_provided|SLC27A5-related_disorder": 5,
    "SLC27A5-related_disorder|not_provided|not_specified": 3,
    "SLC27A5-related_disorder|not_specified|not_provided": 7,
    "not_specified|SLC27A5-related_disorder|not_provided": 3,
    "not_provided|not_specified|SLC27A5-related_disorder": 1,
    "ZBTB45-related_condition": 1,
    "not_provided|TRIM28-related_disorder": 10,
    "not_provided|not_specified|Wilms_tumor_1": 2,
    "WILMS_TUMOR_7": 3,
    "TRIM28-related_disorder|not_provided": 8,
    "TRIM28-related_disorder": 3,
    "TRIM28-related_disorder|not_specified|not_provided": 1,
    "Wilms_tumor_1|not_specified|not_provided": 1,
    "not_specified|TRIM28-related_disorder": 1,
    "Wilms_tumor_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Wilms_tumor_1": 1,
    "Wilms_tumor_1|not_specified": 5,
    "DEFB128-related_disorder": 2,
    "Polyglucosan_body_myopathy_type_1": 386,
    "Inborn_genetic_diseases|Polyglucosan_body_myopathy_type_1|not_provided": 1,
    "not_specified|not_provided|Polyglucosan_body_myopathy_type_1": 1,
    "Polyglucosan_body_myopathy_type_1|Inborn_genetic_diseases": 11,
    "Inborn_genetic_diseases|Polyglucosan_body_myopathy_type_1": 25,
    "Polyglucosan_body_myopathy_1_with_immunodeficiency": 3,
    "Polyglucosan_body_myopathy_type_1|not_provided": 6,
    "RBCK1-related_disorder|Polyglucosan_body_myopathy_type_1|not_provided": 2,
    "Polyglucosan_body_myopathy_type_1|not_specified|not_provided": 3,
    "Polyglucosan_body_myopathy_type_1|not_provided|RBCK1-related_disorder": 1,
    "Polyglucosan_body_myopathy_type_1|not_provided|not_specified": 1,
    "Polyglucosan_body_myopathy_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Polyglucosanbody_Myopathy_Typ_1": 1,
    "Inborn_genetic_diseases|Polyglucosan_body_myopathy_type_1|See_cases": 1,
    "RBCK1-related_disorder": 3,
    "Polyglucosan_body_myopathy_type_1|RBCK1-related_disorder": 3,
    "Polyglucosan_body_myopathy_1_without_immunodeficiency|Polyglucosan_body_myopathy_type_1": 7,
    "RBCK1-related_disorder|Inborn_genetic_diseases|not_provided|Polyglucosan_body_myopathy_type_1": 1,
    "See_cases|Polyglucosan_body_myopathy_type_1": 1,
    "Polyglucosan_body_myopathy_1_without_immunodeficiency": 1,
    "RBCK1-related_disorder|Polyglucosan_body_myopathy_type_1": 1,
    "Glycogen_storage_disease|_type_IV|Polyglucosan_body_myopathy_type_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Polyglucosan_body_myopathy_type_1": 1,
    "Inborn_genetic_diseases|not_provided|Polyglucosan_body_myopathy_type_1": 1,
    "not_provided|TBC1D20-related_disorder": 4,
    "TBC1D20-related_disorder|not_provided|not_specified": 1,
    "Warburg_micro_syndrome_4": 7,
    "Warburg_micro_syndrome_4|Inborn_genetic_diseases": 1,
    "TBC1D20-related_disorder": 2,
    "Warburg_micro_syndrome_4|not_provided": 2,
    "Inborn_genetic_diseases|TBC1D20-related_disorder": 1,
    "not_provided|Warburg_micro_syndrome_4": 1,
    "not_provided|CSNK2A1-related_disorder": 2,
    "Okur-Chung_neurodevelopmental_syndrome|not_provided": 14,
    "Okur-Chung_neurodevelopmental_syndrome": 38,
    "not_provided|CSNK2A1-related_neurodevelopmental_syndrome": 1,
    "CSNK2A1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Okur-Chung_neurodevelopmental_syndrome|Developmental_disorder": 1,
    "not_provided|Okur-Chung_neurodevelopmental_syndrome": 5,
    "Okur-Chung_neurodevelopmental_syndrome|not_provided|Neurodevelopmental_delay|Inborn_genetic_diseases|See_cases": 1,
    "Okur-Chung_neurodevelopmental_syndrome|not_provided|Autism_spectrum_disorder": 1,
    "Okur-Chung_neurodevelopmental_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "CSNK2A1-related_disorder|Okur-Chung_neurodevelopmental_syndrome|not_provided": 1,
    "CSNK2A1-related_disorder|not_provided": 1,
    "Okur-Chung_neurodevelopmental_syndrome|CSNK2A1-related_disorder": 1,
    "not_provided|CSNK2A1-related_disorder|Okur-Chung_neurodevelopmental_syndrome": 1,
    "Okur-Chung_neurodevelopmental_syndrome|not_provided|Intellectual_disability": 1,
    "Okur-Chung_neurodevelopmental_syndrome|Inborn_genetic_diseases": 1,
    "CSNK2A1-related_disorder|not_provided|Okur-Chung_neurodevelopmental_syndrome": 1,
    "Brown-Vialetto-van_Laere_syndrome_1": 269,
    "Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases|not_provided": 7,
    "Brown-Vialetto-van_Laere_syndrome_1|not_provided|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_1": 16,
    "Inborn_genetic_diseases|not_specified|Progressive_bulbar_palsy_of_childhood|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases": 30,
    "Brown-Vialetto-van_Laere_syndrome_1|not_provided": 10,
    "Brown-Vialetto-van_Laere_syndrome_1|SLC52A3-related_disorder": 1,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "not_specified|Brown-Vialetto-van_Laere_syndrome_1": 3,
    "not_specified|Progressive_bulbar_palsy_of_childhood|not_provided|Brown-Vialetto-van_Laere_syndrome_1": 2,
    "Brown-Vialetto-van_Laere_syndrome_1|not_provided|Progressive_bulbar_palsy_of_childhood": 4,
    "Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases|SLC52A3-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Brown-Vialetto-van_Laere_syndrome_1": 4,
    "SLC52A3-related_disorder|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_1|not_specified": 4,
    "Brown-Vialetto-van_Laere_syndrome_1|not_provided|SLC52A3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Brown-Vialetto-van_Laere_syndrome_1|not_specified": 2,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_1|SLC52A3-related_disorder|not_provided": 1,
    "not_specified|Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|SLC52A3-related_disorder|Brown-Vialetto-van_Laere_syndrome_1": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_1": 4,
    "Brown-Vialetto-van_Laere_syndrome_1|not_provided|not_specified|Progressive_bulbar_palsy_of_childhood": 2,
    "Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases|Progressive_bulbar_palsy_of_childhood": 1,
    "Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_1|Progressive_bulbar_palsy_of_childhood": 1,
    "Brown-Vialetto-van_Laere_syndrome_1|Madras_motor_neuron_disease|Inborn_genetic_diseases|Auditory_neuropathy": 1,
    "not_provided|Brown-Vialetto-van_Laere_syndrome_1|SLC52A3-related_disorder": 1,
    "not_specified|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|Progressive_bulbar_palsy_of_childhood|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_1": 2,
    "Brown-Vialetto-van_Laere_syndrome_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Progressive_bulbar_palsy_of_childhood|Brown-Vialetto-van_Laere_syndrome_1": 1,
    "not_specified|Brown-Vialetto-van_Laere_syndrome_1|not_provided|Progressive_bulbar_palsy_of_childhood": 2,
    "not_provided|not_specified|Brown-Vialetto-van_Laere_syndrome_1": 2,
    "SLC52A3-related_disorder|Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases|not_specified": 1,
    "Progressive_bulbar_palsy_of_childhood|SLC52A3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Brown-Vialetto-van_Laere_syndrome_1|not_specified": 1,
    "not_specified|not_provided|Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Brown-Vialetto-van_Laere_syndrome_1": 2,
    "Brown-Vialetto-van_Laere_syndrome_1|Inborn_genetic_diseases|not_specified|SLC52A3-related_disorder|not_provided": 1,
    "Progressive_bulbar_palsy_of_childhood|not_provided|Brown-Vialetto-van_Laere_syndrome_1|not_specified": 1,
    "Progressive_bulbar_palsy_of_childhood|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Brown-Vialetto-van_Laere_syndrome_1|not_provided|SLC52A3-related_disorder": 2,
    "not_provided|Progressive_bulbar_palsy_of_childhood": 1,
    "Inborn_genetic_diseases|not_provided|Brown-Vialetto-van_Laere_syndrome_1|Progressive_bulbar_palsy_of_childhood": 1,
    "SLC52A3-related_disorder|Brown-Vialetto-van_Laere_syndrome_1|Progressive_bulbar_palsy_of_childhood|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Progressive_bulbar_palsy_of_childhood|Brown-Vialetto-van_Laere_syndrome_1|not_provided": 1,
    "SLC52A3-related_disorder": 2,
    "RSPO4-related_disorder": 3,
    "RSPO4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Anonychia|not_provided": 1,
    "Spinocerebellar_ataxia_type_23": 40,
    "Spinocerebellar_ataxia_type_23|not_provided": 8,
    "not_provided|Spinocerebellar_ataxia_type_23": 12,
    "not_provided|Inborn_genetic_diseases|Spinocerebellar_ataxia_type_23": 1,
    "Spinocerebellar_ataxia_type_23|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_type_23|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_23": 2,
    "not_provided|Spinocerebellar_ataxia_type_23|not_specified": 2,
    "not_specified|Spinocerebellar_ataxia_type_23|not_provided": 1,
    "Spinocerebellar_ataxia_type_23|not_specified|not_provided": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_23": 3,
    "Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_23": 1,
    "not_specified|not_provided|PDYN-related_disorder": 2,
    "TGM3-related_disorder": 20,
    "not_provided|TGM3-related_disorder": 2,
    "Uncombable_hair_syndrome_2": 1,
    "TGM3-related_disorder|not_provided": 1,
    "Spinocerebellar_ataxia_type_35": 36,
    "Spinocerebellar_ataxia_type_35|TGM6-related_disorder|not_provided|not_specified": 1,
    "Spinocerebellar_ataxia_type_35|TGM6-related_disorder|not_specified|not_provided": 2,
    "Spinocerebellar_ataxia_type_35|not_provided": 13,
    "TGM6-related_disorder|not_provided|Spinocerebellar_ataxia_type_35": 1,
    "Spinocerebellar_ataxia_type_35|not_specified|not_provided": 5,
    "Spinocerebellar_ataxia_type_35|Myopathic_facies|Rigidity|Oculomotor_apraxia|Axial_muscle_stiffness|Parkinsonian_disorder": 1,
    "TGM6-related_disorder|Inborn_genetic_diseases|not_provided|Spinocerebellar_ataxia_type_35": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|TGM6-related_disorder": 1,
    "TGM6-related_disorder|not_provided": 1,
    "not_specified|Spinocerebellar_ataxia_type_35|not_provided": 9,
    "not_provided|TGM6-related_disorder": 2,
    "not_specified|not_provided|TGM6-related_disorder|Spinocerebellar_ataxia_type_35": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_35": 3,
    "not_provided|Spinocerebellar_ataxia_type_35": 17,
    "TGM6-related_disorder|Spinocerebellar_ataxia_type_35|not_specified|not_provided": 2,
    "TGM6-related_disorder|Spinocerebellar_ataxia_type_35|not_provided|not_specified": 2,
    "Spinocerebellar_ataxia_type_35|not_provided|Inborn_genetic_diseases": 2,
    "TGM6-related_disorder": 7,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_35": 2,
    "not_provided|not_specified|TGM6-related_disorder": 2,
    "Spinocerebellar_ataxia_type_35|Inborn_genetic_diseases": 1,
    "not_provided|Spinocerebellar_ataxia_type_35|not_specified": 5,
    "Spinocerebellar_ataxia_type_35|Polyneuropathy|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia_type_35|not_provided": 1,
    "Vascular_parkinsonism|Parkinsonian_disorder|Parkinson_disease|not_provided": 1,
    "not_provided|not_specified|Spinocerebellar_ataxia_type_35": 3,
    "Spinocerebellar_ataxia_type_35|not_specified": 1,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_35|Inborn_genetic_diseases": 1,
    "Vascular_parkinsonism|Parkinson_disease|Parkinsonian_disorder|Spinocerebellar_ataxia_type_35|not_specified|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia_type_35|TGM6-related_disorder": 1,
    "Spinocerebellar_ataxia_type_35|not_provided|not_specified": 2,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_35|Acute_myeloid_leukemia": 1,
    "TGM6-related_disorder|Spinocerebellar_ataxia_type_35|not_provided": 1,
    "SNRPB-related_disorder": 2,
    "not_provided|SNRPB-related_disorder": 2,
    "Isolated_Pierre-Robin_syndrome|Intellectual_disability": 1,
    "Cerebro-costo-mandibular_syndrome|not_provided": 1,
    "SNRPB-related_disorder|not_provided": 2,
    "not_provided|SNRPB-related_disorder|Cerebro-costo-mandibular_syndrome": 1,
    "NOP56-related_disorder": 11,
    "not_provided|NOP56-related_disorder": 1,
    "Cerebellar_ataxia|Mild_global_developmental_delay": 1,
    "Spinocerebellar_ataxia_type_36": 2,
    "IDH3B-related_disorder": 1,
    "not_provided|Retinitis_pigmentosa_46": 3,
    "not_provided|Retinitis_Pigmentosa|_Recessive|Retinal_dystrophy|Retinitis_pigmentosa_46": 1,
    "IDH3B-related_disorder|not_provided": 1,
    "Retinitis_pigmentosa_46": 6,
    "not_provided|IDH3B-related_disorder|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_46|not_provided|not_specified": 1,
    "Retinitis_pigmentosa|Optic_atrophy|Retinal_dystrophy|not_specified|not_provided": 1,
    "Retinitis_pigmentosa_46|not_provided": 3,
    "Retinitis_pigmentosa|not_provided|Retinitis_pigmentosa_46": 1,
    "IDH3B-related_disorder|not_specified|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|IDH3B-related_disorder": 1,
    "Dystonia_30": 18,
    "Inborn_genetic_diseases|VPS16-related_disorder": 3,
    "Coarse_facial_features|Splenomegaly|Decreased_total_neutrophil_count|Peripheral_neuropathy": 1,
    "Dystonia_30|not_provided": 3,
    "Inborn_genetic_diseases|Dystonia_30": 1,
    "VPS16-related_disorder|not_provided": 1,
    "Dystonia_30|VPS16-associated_disorder": 1,
    "not_provided|Dystonia_30": 1,
    "VPS16-related_disorder": 2,
    "not_provided|VPS16-related_disorder": 1,
    "Neurohypophyseal_diabetes_insipidus": 42,
    "Neurohypophyseal_diabetes_insipidus|not_provided": 11,
    "Neurohypophyseal_diabetes_insipidus|Inborn_genetic_diseases": 2,
    "not_provided|Neurohypophyseal_diabetes_insipidus": 4,
    "AVP-related_disorder": 1,
    "Diabetes_insipidus|Neurohypophyseal_diabetes_insipidus|not_provided": 1,
    "not_provided|AVP-related_disorder": 2,
    "Neurohypophyseal_diabetes_insipidus|AVP-related_disorder": 1,
    "AVP-related_disorder|Neurohypophyseal_diabetes_insipidus": 1,
    "early-onset_neurohypophyseal_diabetes_insipidus": 1,
    "not_provided|Neurohypophyseal_diabetes_insipidus|AVP-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Neurohypophyseal_diabetes_insipidus": 1,
    "Inborn_genetic_diseases|Neurohypophyseal_diabetes_insipidus": 1,
    "AVP-related_disorder|not_provided|Neurohypophyseal_diabetes_insipidus": 1,
    "Diabetes_insipidus|_neurohypophyseal|_autosomal_recessive": 1,
    "DDRGK1-related_disorder|not_provided": 1,
    "not_provided|Spondyloepimetaphyseal_dysplasia|_Shohat_type": 2,
    "not_provided|DDRGK1-related_disorder": 2,
    "Spondyloepimetaphyseal_dysplasia|_Shohat_type": 1,
    "Inosine_triphosphatase_deficiency": 203,
    "Inosine_triphosphatase_deficiency|Developmental_and_epileptic_encephalopathy|_35": 3,
    "Developmental_and_epileptic_encephalopathy|_35": 14,
    "peginterferon_alfa-2b_and_ribavirin_response_-_Toxicity|not_provided|Inosine_triphosphatase_deficiency|not_specified": 1,
    "not_provided|Inosine_triphosphatase_deficiency": 10,
    "not_provided|Inosine_triphosphatase_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Inosine_triphosphatase_deficiency|Developmental_and_epileptic_encephalopathy|_35": 2,
    "Developmental_and_epileptic_encephalopathy|_35|Inosine_triphosphatase_deficiency": 7,
    "peginterferon_alfa-2b_and_ribavirin_response_-_Toxicity|not_provided|Developmental_and_epileptic_encephalopathy|_35|Inosine_triphosphatase_deficiency": 1,
    "Inosine_triphosphatase_deficiency|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_35|not_specified|Inosine_triphosphatase_deficiency|not_provided": 2,
    "Inosine_triphosphatase_deficiency|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Inosine_triphosphatase_deficiency": 3,
    "not_provided|Inosine_triphosphatase_deficiency|ITPA-related_disorder": 1,
    "Infantile_epileptic_dyskinetic_encephalopathy|Inosine_triphosphatase_deficiency": 1,
    "not_specified|Inosine_triphosphatase_deficiency|Developmental_and_epileptic_encephalopathy|_35|not_provided": 1,
    "Inosine_triphosphatase_deficiency|ITPA-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_35|Hypodontia|not_provided|Inosine_triphosphatase_deficiency": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_35|Inosine_triphosphatase_deficiency": 1,
    "Developmental_and_epileptic_encephalopathy|_35|not_provided|Inosine_triphosphatase_deficiency": 1,
    "ITPA-related_disorder|Inosine_triphosphatase_deficiency": 2,
    "Inosine_triphosphatase_deficiency|Developmental_and_epileptic_encephalopathy|_35|not_provided": 1,
    "ITPA-related_disorder|Inosine_triphosphatase_deficiency|Infantile_epileptic_dyskinetic_encephalopathy|Developmental_and_epileptic_encephalopathy|_35": 1,
    "ITPA-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_35|Inosine_triphosphatase_deficiency": 1,
    "ITPA-related_disorder": 1,
    "not_provided|Corneal_dystrophy-perceptive_deafness_syndrome": 33,
    "not_provided|Corneal_dystrophy|_Fuchs_endothelial|_4|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4": 3,
    "not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome": 67,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "not_provided|SLC4A11-related_disorder|Corneal_dystrophy|not_specified|Posterior_polymorphous_corneal_dystrophy_1|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4|Corneal_dystrophy-perceptive_deafness_syndrome|not_provided": 2,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|not_provided": 9,
    "Corneal_dystrophy-perceptive_deafness_syndrome|not_provided": 30,
    "Corneal_dystrophy-perceptive_deafness_syndrome|not_provided|Corneal_dystrophy|not_specified|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Corneal_dystrophy|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome": 7,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4|not_provided": 5,
    "not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4": 6,
    "Corneal_dystrophy|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Inborn_genetic_diseases|Corneal_dystrophy|not_provided": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|not_provided": 2,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|not_provided|Corneal_dystrophy|_Fuchs_endothelial|_4": 1,
    "Corneal_dystrophy|_Fuchs_endothelial|_4|not_specified|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|not_provided": 1,
    "not_specified|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Corneal_dystrophy|not_specified|not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4|Corneal_dystrophy-perceptive_deafness_syndrome": 8,
    "SLC4A11-related_disorder|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4": 1,
    "not_provided|SLC4A11-related_disorder": 3,
    "Corneal_dystrophy|_Fuchs_endothelial|_4": 2,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4": 3,
    "not_provided|Corneal_dystrophy|Inborn_genetic_diseases": 1,
    "Corneal_dystrophy|SLC4A11-related_disorder|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "Inborn_genetic_diseases|Corneal_dystrophy|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|not_provided|Corneal_dystrophy|not_specified": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4": 4,
    "not_provided|SLC4A11-related_disorder|Corneal_dystrophy-perceptive_deafness_syndrome": 3,
    "Corneal_dystrophy|Corneal_dystrophy-perceptive_deafness_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|Corneal_dystrophy|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|not_specified": 1,
    "not_provided|Corneal_Dystrophy|_Recessive": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|not_provided|Corneal_dystrophy": 1,
    "not_specified|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|not_provided|Corneal_dystrophy": 2,
    "Corneal_dystrophy-perceptive_deafness_syndrome|SLC4A11-related_disorder|Corneal_dystrophy|not_provided": 3,
    "not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea": 6,
    "SLC4A11-related_disorder|not_provided": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|not_provided": 4,
    "Corneal_dystrophy-perceptive_deafness_syndrome|not_provided|Corneal_dystrophy": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Inborn_genetic_diseases": 2,
    "Corneal_dystrophy|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "not_specified|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|_Fuchs_endothelial|_4": 2,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|not_provided": 2,
    "Corneal_dystrophy|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|Congenital_hereditary_endothelial_dystrophy_of_cornea|not_provided": 1,
    "not_specified|not_provided|Corneal_dystrophy|_Fuchs_endothelial|_4": 1,
    "Inborn_genetic_diseases|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4|Congenital_hereditary_endothelial_dystrophy_of_cornea|not_provided": 1,
    "Corneal_dystrophy|Inborn_genetic_diseases|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome": 2,
    "not_specified|Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy|not_provided": 1,
    "not_provided|SLC4A11-related_disorder|Corneal_dystrophy|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy": 1,
    "not_specified|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|not_provided": 1,
    "not_provided|Corneal_dystrophy|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "SLC4A11-related_disorder": 4,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Inborn_genetic_diseases": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome": 2,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea|not_specified|Corneal_dystrophy|not_provided": 1,
    "not_provided|SLC4A11-related_disorder|Corneal_dystrophy": 1,
    "SLC4A11-related_disorder|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome": 1,
    "not_specified|not_provided|Corneal_dystrophy": 1,
    "not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|not_specified|Corneal_dystrophy|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|_Fuchs_endothelial|_4": 1,
    "not_provided|not_specified|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "SLC4A11-related_disorder|not_provided|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Corneal_dystrophy|not_provided": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|not_provided|not_specified": 1,
    "Corneal_dystrophy-perceptive_deafness_syndrome|Congenital_hereditary_endothelial_dystrophy_of_cornea": 3,
    "Inborn_genetic_diseases|not_provided|Corneal_dystrophy": 1,
    "not_specified|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|not_provided|Congenital_hereditary_endothelial_dystrophy_of_cornea": 1,
    "not_provided|Corneal_dystrophy|_Fuchs_endothelial|_4": 1,
    "Congenital_hereditary_endothelial_dystrophy_of_cornea|Corneal_dystrophy-perceptive_deafness_syndrome|Corneal_dystrophy|not_provided": 1,
    "ATRN-related_disorder": 13,
    "not_provided|ATRN-related_disorder": 12,
    "Autism|Thrombocytopenia|Global_developmental_delay": 1,
    "ATRN-related_disorder|not_provided": 11,
    "ATRN-related_disorder|not_specified": 2,
    "not_specified|not_provided|Pigmentary_pallidal_degeneration": 2,
    "PANK2-related_disorder": 3,
    "Pigmentary_pallidal_degeneration": 499,
    "Pigmentary_pallidal_degeneration|Inborn_genetic_diseases": 11,
    "not_provided|Pigmentary_pallidal_degeneration": 30,
    "PANK2-related_disorder|Pigmentary_pallidal_degeneration": 3,
    "Pigmentary_pallidal_degeneration|not_provided": 29,
    "Inborn_genetic_diseases|not_specified|Pigmentary_pallidal_degeneration": 1,
    "Inborn_genetic_diseases|Pigmentary_pallidal_degeneration": 9,
    "Retinal_dystrophy|Pigmentary_pallidal_degeneration": 1,
    "Pigmentary_pallidal_degeneration|Inborn_genetic_diseases|not_provided": 1,
    "Pigmentary_pallidal_degeneration|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Pigmentary_pallidal_degeneration": 3,
    "not_provided|Pigmentary_pallidal_degeneration|not_specified": 2,
    "PANK2-related_disorder|not_provided|Pigmentary_pallidal_degeneration": 1,
    "Inborn_genetic_diseases|Pigmentary_pallidal_degeneration|not_provided": 1,
    "Pigmentary_pallidal_degeneration|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Pigmentary_pallidal_degeneration|not_provided": 1,
    "Pigmentary_pallidal_degeneration|See_cases": 1,
    "not_provided|not_specified|Pigmentary_pallidal_degeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration": 1,
    "PANK2-related_disorder|not_specified|not_provided|Pigmentary_pallidal_degeneration": 1,
    "Pigmentary_pallidal_degeneration|not_specified": 3,
    "not_specified|Pigmentary_pallidal_degeneration": 4,
    "Pigmentary_pallidal_degeneration|PANK2-related_disorder": 1,
    "Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration|Pigmentary_pallidal_degeneration|not_provided": 2,
    "Pigmentary_pallidal_degeneration|Retinal_dystrophy|not_provided": 1,
    "Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration": 3,
    "Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration|Pigmentary_pallidal_degeneration|See_cases": 1,
    "Pigmentary_pallidal_degeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration": 3,
    "Pigmentary_pallidal_degeneration|PANK2-related_disorder|not_provided": 1,
    "not_provided|not_specified|Pigmentary_pallidal_degeneration": 2,
    "not_provided|Pigmentary_pallidal_degeneration|Inborn_genetic_diseases": 2,
    "Neurodegeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration": 1,
    "not_provided|PANK2-related_disorder|Pigmentary_pallidal_degeneration": 1,
    "Pigmentary_pallidal_degeneration|not_provided|Inborn_genetic_diseases": 1,
    "Neurodegeneration|Pigmentary_pallidal_degeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration": 1,
    "not_provided|Inborn_genetic_diseases|Pigmentary_pallidal_degeneration": 1,
    "Pigmentary_pallidal_degeneration|not_provided|Leber_congenital_amaurosis": 1,
    "Cone-rod_dystrophy|Pigmentary_pallidal_degeneration": 1,
    "Pigmentary_pallidal_degeneration|not_specified|PANK2-related_disorder": 1,
    "Dystonic_disorder|Pigmentary_pallidal_degeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration|not_provided": 1,
    "Pigmentary_pallidal_degeneration|Dystonic_disorder": 1,
    "Inborn_genetic_diseases|Pigmentary_pallidal_degeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration|not_provided|Retinitis_pigmentosa|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "PANK2-related_disorder|Inborn_genetic_diseases|not_provided|Pigmentary_pallidal_degeneration|Hypoprebetalipoproteinemia|_acanthocytosis|_retinitis_pigmentosa|_and_pallidal_degeneration": 1,
    "Inherited_prion_disease": 28,
    "not_provided|Inherited_prion_disease": 5,
    "Inherited_prion_disease|Huntington_disease-like_1": 2,
    "Huntington_disease-like_1": 53,
    "not_provided|Huntington_disease-like_1": 4,
    "not_provided|Inherited_prion_disease|Huntington_disease-like_1": 2,
    "PRNP-associated_condition": 1,
    "Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|Fatal_familial_insomnia|Spongiform_encephalopathy_with_neuropsychiatric_features|Inherited_Creutzfeldt-Jakob_disease|Kuru|_susceptibility_to|not_provided|Inherited_prion_disease": 1,
    "Inherited_Creutzfeldt-Jakob_disease|Gerstmann-Straussler-Scheinker_syndrome|Spongiform_encephalopathy_with_neuropsychiatric_features|Fatal_familial_insomnia|Huntington_disease-like_1|Kuru|_susceptibility_to|not_provided|Inherited_prion_disease": 1,
    "Spongiform_encephalopathy_with_neuropsychiatric_features": 3,
    "not_provided|Huntington_disease-like_1|Inherited_prion_disease": 1,
    "Huntington_disease-like_1|not_specified": 1,
    "Gerstmann-Straussler-Scheinker_syndrome": 5,
    "Huntington_disease-like_1|not_provided": 2,
    "not_specified|not_provided|Inherited_prion_disease|Huntington_disease-like_1": 1,
    "Inherited_prion_disease|Huntington_disease-like_1|not_provided": 2,
    "Inherited_prion_disease|not_provided": 2,
    "not_specified|Huntington_disease-like_1": 1,
    "not_provided|Huntington_disease-like_1|Spongiform_encephalopathy_with_neuropsychiatric_features|Inherited_Creutzfeldt-Jakob_disease|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "not_provided|Spongiform_encephalopathy_with_neuropsychiatric_features|Inherited_Creutzfeldt-Jakob_disease|Gerstmann-Straussler-Scheinker_syndrome|Fatal_familial_insomnia|Huntington_disease-like_1|Kuru|_susceptibility_to": 1,
    "not_provided|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "Inborn_genetic_diseases|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "Inherited_prion_disease|Huntington_disease-like_1|not_specified|not_provided": 1,
    "Inherited_prion_disease|not_provided|Huntington_disease-like_1": 2,
    "Kuru|_protection_against": 1,
    "Inherited_Creutzfeldt-Jakob_disease|Fatal_familial_insomnia|Kuru|_susceptibility_to|Spongiform_encephalopathy_with_neuropsychiatric_features|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|not_provided|not_specified|Inherited_prion_disease|.|.|.|Autism_spectrum_disorder": 1,
    "Gerstmann-Straussler-Scheinker_syndrome|Huntington_disease-like_1": 2,
    "CEREBRAL_AMYLOID_ANGIOPATHY|_PRNP-RELATED": 2,
    "Inherited_Creutzfeldt-Jakob_disease|Huntington_disease-like_1": 1,
    "Inborn_genetic_diseases|Huntington_disease-like_1|not_provided": 1,
    "CEREBRAL_AMYLOID_ANGIOPATHY|_PRNP-RELATED|Huntington_disease-like_1": 1,
    "Inherited_prion_disease|Inborn_genetic_diseases": 1,
    "Huntington_disease-like_1|Inherited_Creutzfeldt-Jakob_disease|Gerstmann-Straussler-Scheinker_syndrome|Fatal_familial_insomnia|Kuru|_susceptibility_to|Spongiform_encephalopathy_with_neuropsychiatric_features": 1,
    "not_provided|Spongiform_encephalopathy_with_neuropsychiatric_features|Huntington_disease-like_1|Inherited_prion_disease|not_specified": 1,
    "Huntington_disease-like_1|Inborn_genetic_diseases": 1,
    "Spongiform_encephalopathy_with_neuropsychiatric_features|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|not_provided|Fatal_familial_insomnia": 1,
    "Kuru|_susceptibility_to|Spongiform_encephalopathy_with_neuropsychiatric_features|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|Inherited_Creutzfeldt-Jakob_disease|Fatal_familial_insomnia|Inherited_prion_disease": 1,
    "Huntington_disease-like_1|Spongiform_encephalopathy_with_neuropsychiatric_features": 1,
    "Spongiform_encephalopathy_with_neuropsychiatric_features|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "Inherited_prion_disease|not_specified|not_provided": 1,
    "not_provided|Gerstmann-Straussler-Scheinker_syndrome|Huntington_disease-like_1": 1,
    "Kuru|_susceptibility_to|Spongiform_encephalopathy_with_neuropsychiatric_features|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|Inherited_Creutzfeldt-Jakob_disease|Fatal_familial_insomnia|not_provided": 1,
    "PRNP-related_disorder|not_provided|Huntington_disease-like_1|Inherited_Creutzfeldt-Jakob_disease": 1,
    "Inborn_genetic_diseases|Kuru|_susceptibility_to|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|Inherited_Creutzfeldt-Jakob_disease|Spongiform_encephalopathy_with_neuropsychiatric_features|Fatal_familial_insomnia": 1,
    "Inherited_Creutzfeldt-Jakob_disease": 1,
    "Huntington_disease-like_1|Fatal_familial_insomnia|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "Fatal_familial_insomnia|Huntington_disease-like_1|Kuru|_susceptibility_to|Inherited_Creutzfeldt-Jakob_disease|Gerstmann-Straussler-Scheinker_syndrome|Spongiform_encephalopathy_with_neuropsychiatric_features": 1,
    "PRNP-related_disorder|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome": 1,
    "not_provided|Inherited_prion_disease|Huntington_disease-like_1|Reclassified_-_variant_of_unknown_significance": 1,
    "CEREBRAL_AMYLOID_ANGIOPATHY|_PRNP-RELATED|not_provided": 1,
    "Kuru|_susceptibility_to|Huntington_disease-like_1|Gerstmann-Straussler-Scheinker_syndrome|Inherited_Creutzfeldt-Jakob_disease|Spongiform_encephalopathy_with_neuropsychiatric_features|Fatal_familial_insomnia": 1,
    "Inborn_genetic_diseases|Huntington_disease-like_1": 1,
    "PRNP-related_disorder": 1,
    "Gerstmann-Straussler-Scheinker_syndrome|Fatal_familial_insomnia|Spongiform_encephalopathy_with_neuropsychiatric_features|Inherited_Creutzfeldt-Jakob_disease|Huntington_disease-like_1|Kuru|_susceptibility_to|not_provided|Inherited_prion_disease": 1,
    "TMEM230-related_disorder": 4,
    "PCNA-related_disorder|not_provided": 1,
    "Ataxia-telangiectasia-like_disorder_2": 2,
    "PCNA-related_disorder": 2,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 57,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_provided": 12,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_provided|not_specified": 4,
    "not_specified|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_provided": 1,
    "not_provided|PROKR2-related_disorder": 2,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 6,
    "not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 13,
    "Amenorrhea|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "not_provided|PROKR2-related_disorder|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "PROKR2-related_disorder": 3,
    "not_provided|not_specified|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 3,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_provided|Male_infertility_with_spermatogenesis_disorder|Hypogonadotropic_hypogonadism": 1,
    "PROKR2-related_disorder|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_specified": 1,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|Hypogonadotropic_hypogonadism_3_without_anosmia|not_provided": 1,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_specified": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "not_provided|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|not_specified|not_provided": 1,
    "Hypogonadotropic_hypogonadism|not_specified|not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|Infertility_disorder": 1,
    "not_specified|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 2,
    "PROKR2-related_disorder|not_specified|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|Inborn_genetic_diseases|not_provided": 1,
    "PROKR2-related_disorder|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "Amenorrhea|not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|PROKR2-related_disorder|not_provided|not_specified": 1,
    "PROKR2-related_disorder|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|not_specified|not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|Hypogonadism_with_anosmia|Amenorrhea": 1,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|PROKR2-related_disorder|not_provided|Hypogonadotropic_hypogonadism_3_without_anosmia|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|not_specified": 1,
    "Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "not_specified|Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia": 1,
    "PROKR2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Hypogonadotropic_hypogonadism_3_with_or_without_anosmia|Hypogonadotropic_hypogonadism_2_with_or_without_anosmia": 1,
    "CHGB-related_disorder": 7,
    "CHGB-related_disorder|not_provided": 2,
    "CHGB-related_disorder|not_specified": 1,
    "Premature_ovarian_failure_10": 11,
    "Premature_ovarian_failure_10|not_provided": 1,
    "MCM8-related_disorder|not_specified|not_provided": 1,
    "not_provided|Premature_ovarian_failure_10": 1,
    "Premature_ovarian_failure_10|Azoospermia": 1,
    "MCM8-related_disorder": 5,
    "Combined_oxidative_phosphorylation_deficiency_57": 3,
    "Kindler_syndrome": 114,
    "not_provided|Kindler_syndrome": 38,
    "Kindler_syndrome|not_provided": 23,
    "not_provided|FERMT1-related_disorder": 3,
    "Kindler_syndrome|FERMT1-related_disorder|not_provided": 4,
    "Kindler_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Kindler_syndrome": 2,
    "FERMT1-related_disorder|not_provided": 4,
    "Kindler_syndrome|not_specified|not_provided": 1,
    "not_provided|Kindler_syndrome|Inborn_genetic_diseases": 1,
    "FERMT1-related_disorder|not_provided|Kindler_syndrome": 1,
    "not_provided|Kindler_syndrome|not_specified": 3,
    "Kindler_syndrome|not_provided|not_specified": 3,
    "not_specified|Kindler_syndrome": 1,
    "not_provided|FERMT1-related_disorder|Kindler_syndrome": 2,
    "Kindler_syndrome|not_provided|FERMT1-related_disorder": 3,
    "not_provided|Kindler_syndrome|FERMT1-related_disorder": 1,
    "Inborn_genetic_diseases|Kindler_syndrome|not_provided": 1,
    "not_specified|Kindler_syndrome|not_provided": 1,
    "FERMT1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_1": 6,
    "not_provided|Type_A2_brachydactyly|Inborn_genetic_diseases": 1,
    "BMP2-related_disorder": 7,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_1|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies": 2,
    "BMP2-related_disorder|not_provided": 4,
    "not_provided|Ventricular_septal_defect_1|not_specified": 1,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies": 2,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_1|not_provided": 4,
    "Type_A2_brachydactyly": 2,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies|not_specified|not_provided": 1,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies|not_provided": 1,
    "not_provided|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_1": 1,
    "not_provided|not_specified|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies": 1,
    "Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies|Type_A2_brachydactyly|not_provided": 1,
    "PDA1": 1,
    "not_provided|Short_stature|_facial_dysmorphism|_and_skeletal_anomalies_with_or_without_cardiac_anomalies_1": 1,
    "not_provided|BMP2-related_disorder": 2,
    "glycolate_oxidase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|PLCB1-related_disorder|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Developmental_and_epileptic_encephalopathy|_12|PLCB1-related_disorder|Inborn_genetic_diseases": 4,
    "Developmental_and_epileptic_encephalopathy|_12|PLCB1-related_disorder": 5,
    "not_specified|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12": 1,
    "PLCB1-related_disorder|Developmental_and_epileptic_encephalopathy|_12": 4,
    "Developmental_and_epileptic_encephalopathy|_12|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_12|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|not_specified|PLCB1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|PLCB1-related_disorder|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Developmental_and_epileptic_encephalopathy|_12": 1,
    "PLCB1-related_disorder|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_12|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12|not_provided|not_specified": 1,
    "not_specified|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_12|not_specified": 1,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_provided|PLCB1-related_disorder|Developmental_and_epileptic_encephalopathy|_12": 1,
    "Inborn_genetic_diseases|not_specified|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|See_cases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases|not_specified|not_provided|PLCB1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_12|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 1,
    "not_specified|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12|not_provided": 2,
    "Inborn_genetic_diseases|PLCB1-related_disorder|Developmental_and_epileptic_encephalopathy|_12|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|PLCB1-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_12|not_provided": 1,
    "not_provided|not_specified|Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|Developmental_and_epileptic_encephalopathy|_12|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_12|not_specified|not_provided": 1,
    "PLCB1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_12": 2,
    "Early_Infantile_Epileptic_Encephalopathy|_Autosomal_Recessive|not_provided": 7,
    "Auriculocondylar_syndrome_2": 74,
    "not_provided|Auriculocondylar_syndrome_2": 20,
    "PLCB4-related_disorder": 8,
    "Inborn_genetic_diseases|not_provided|Auriculocondylar_syndrome_2": 1,
    "Auriculocondylar_syndrome_2|not_provided": 11,
    "Auriculocondylar_syndrome_2B|Auriculocondylar_syndrome_2": 2,
    "PLCB4-related_disorder|not_provided": 3,
    "PLCB4-related_disorder|not_provided|Auriculocondylar_syndrome_2": 3,
    "not_provided|PLCB4-related_disorder|Auriculocondylar_syndrome_2": 2,
    "not_provided|PLCB4-related_disorder": 1,
    "Auriculocondylar_syndrome_2B": 1,
    "Inborn_genetic_diseases|Auriculocondylar_syndrome_2": 3,
    "Auriculocondylar_syndrome_1|Auriculocondylar_syndrome_2|not_provided": 1,
    "Inborn_genetic_diseases|Auriculocondylar_syndrome|Auriculocondylar_syndrome_1|Auriculocondylar_syndrome_2|not_provided": 1,
    "Auriculocondylar_syndrome_2|Auriculocondylar_syndrome_1": 2,
    "Inborn_genetic_diseases|Auriculocondylar_syndrome_2|Abnormal_facial_shape|not_provided": 1,
    "Uveal_melanoma|Ocular_melanocytosis": 1,
    "Auriculocondylar_syndrome_2|Inborn_genetic_diseases": 4,
    "Auriculocondylar_syndrome_2|not_provided|PLCB4-related_disorder": 1,
    "Auriculocondylar_syndrome": 6,
    "Congenital_myasthenic_syndrome_18": 136,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_18": 5,
    "Congenital_myasthenic_syndrome_18|Inborn_genetic_diseases|SNAP25-related_disorder|not_provided": 1,
    "Congenital_myasthenic_syndrome_18|not_specified": 4,
    "SNAP25-related_disorder": 2,
    "Congenital_myasthenic_syndrome_18|SNAP25-related_disorder": 1,
    "Congenital_myasthenic_syndrome_18|not_provided": 4,
    "Congenital_myasthenic_syndrome_18|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|SNAP25-related_disorder|Congenital_myasthenic_syndrome_18": 1,
    "Developmental_and_epileptic_encephalopathy|Global_developmental_delay": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_18": 1,
    "SNAP25-related_developmental_delays_and_epileptic_encephalopathies": 1,
    "Developmental_and_epileptic_encephalopathy|Unilateral_Hypotonia|Epilepsy_with_generalized_tonic-clonic_seizures|Focal_epilepsy|Intellectual_disability|not_provided": 1,
    "Congenital_myasthenic_syndrome_18|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Congenital_myasthenic_syndrome_18|not_provided": 1,
    "Congenital_myasthenic_syndrome_18|Developmental_and_epileptic_encephalopathy": 2,
    "not_provided|Congenital_myasthenic_syndrome_18": 3,
    "not_provided|Congenital_myasthenic_syndrome_18|SNAP25-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_myasthenic_syndrome_18": 2,
    "Congenital_myasthenic_syndrome_18|SNAP25-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_myasthenic_syndrome_18|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Congenital_myasthenic_syndrome_18": 3,
    "Inborn_genetic_diseases|SNAP25-related_disorder|Congenital_myasthenic_syndrome_18": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_myasthenic_syndrome_18": 2,
    "Congenital_myasthenic_syndrome_18|not_provided|SNAP25-related_early-onset_developmental_and_epileptic_encephalopathy|Neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|SNAP25-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|SNAP25_related_neurodevelopmental_disorder|Congenital_myasthenic_syndrome_18": 1,
    "Developmental_and_epileptic_encephalopathy|Intellectual_disability|_severe": 1,
    "Seizure|Global_developmental_delay|Optic_atrophy|Stereotypic_movement_disorder|Microcephaly|Developmental_and_epileptic_encephalopathy": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 16,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|not_provided": 2,
    "Bardet-Biedl_syndrome_6|not_provided|McKusick-Kaufman_syndrome": 1,
    "not_provided|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_specified": 1,
    "not_provided|not_specified|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome": 40,
    "not_provided|MKKS-related_disorder": 1,
    "MKKS-related_disorder": 42,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 165,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 12,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 95,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|MKKS-related_disorder": 8,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder": 1,
    "McKusick-Kaufman_syndrome": 4,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_6|not_provided|MKKS-related_disorder": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|not_specified|not_provided|Bardet-Biedl_syndrome_6": 3,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6": 11,
    "MKKS-related_disorder|not_specified|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_6": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 6,
    "MKKS-related_disorder|not_provided|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 1,
    "Bardet-Biedl_syndrome_6": 29,
    "Inborn_genetic_diseases|MKKS-related_disorder": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder|Bardet-Biedl_syndrome": 2,
    "BARDET-BIEDL_SYNDROME_2/6|_DIGENIC": 2,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 7,
    "MKKS-related_disorder|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome": 3,
    "MKKS-related_disorder|Retinal_dystrophy|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_provided|not_specified": 1,
    "not_provided|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome": 2,
    "not_provided|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_specified": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|MKKS-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|MKKS-related_disorder|Bardet-Biedl_syndrome_6": 4,
    "Retinal_dystrophy|not_provided|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 15,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|MKKS-related_disorder": 8,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_provided|Bardet-Biedl_syndrome": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 2,
    "not_provided|McKusick-Kaufman_syndrome": 1,
    "MKKS-related_disorder|not_provided": 1,
    "not_provided|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|MKKS-related_disorder": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Inborn_genetic_diseases|not_provided|Retinal_dystrophy|Bardet-Biedl_syndrome|MKKS-related_disorder": 1,
    "Inborn_genetic_diseases|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_6|Inborn_genetic_diseases|MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|MKKS-related_disorder|Bardet-Biedl_syndrome": 1,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 2,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided": 1,
    "Progressive_cone_dystrophy_(without_rod_involvement)|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 1,
    "MKKS-related_disorder|Inborn_genetic_diseases|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 4,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|MKKS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Bardet-Biedl_syndrome_6|MKKS-related_disorder|not_specified|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 7,
    "MKKS-related_disorder|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|not_provided|Bardet-Biedl_syndrome": 1,
    "not_specified|MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 2,
    "Inborn_genetic_diseases|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|not_provided": 1,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_specified": 1,
    "not_specified|not_provided|McKusick-Kaufman_syndrome": 1,
    "not_specified|not_provided|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 1,
    "Bardet-Biedl_syndrome_1|_modifier_of": 1,
    "Polycystic_kidney_disease|Multicystic_kidney_dysplasia|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "Retinal_dystrophy|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 3,
    "MKKS-related_disorder|Inborn_genetic_diseases|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder": 1,
    "not_provided|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 3,
    "MKKS-related_disorder|Inborn_genetic_diseases|not_specified|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome": 1,
    "McKusick-Kaufman_syndrome|MKKS-related_disorder|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|not_provided|MKKS-related_disorder": 1,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome": 2,
    "Bardet-Biedl_syndrome_6|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_6|Retinal_dystrophy|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|MKKS-related_disorder": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Inborn_genetic_diseases": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_provided|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome": 2,
    "Bardet-Biedl_syndrome_6|not_provided|Retinal_dystrophy": 1,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|not_provided": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|not_provided|not_specified": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_provided|MKKS-related_disorder|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Inborn_genetic_diseases": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_specified|Bardet-Biedl_syndrome|MKKS-related_disorder|not_provided": 1,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6|Inborn_genetic_diseases|McKusick-Kaufman_syndrome": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Inborn_genetic_diseases|MKKS-related_disorder": 1,
    "MKKS-related_disorder|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Inborn_genetic_diseases": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder|Retinal_dystrophy|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "Bardet-Biedl_syndrome_6|Inborn_genetic_diseases|MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|MKKS-related_disorder": 1,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome_6": 1,
    "Bardet-Biedl_syndrome_6|MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "Inborn_genetic_diseases|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|MKKS-related_disorder": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|MKKS-related_disorder": 2,
    "Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Inborn_genetic_diseases|Bardet-Biedl_syndrome": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6|not_provided": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|not_provided": 1,
    "MKKS-related_disorder|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|MKKS-related_disorder": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_specified|not_provided|Bardet-Biedl_syndrome_6|MKKS-related_disorder": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|not_specified|Bardet-Biedl_syndrome|not_provided": 1,
    "MKKS-related_disorder|not_provided|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Bardet-Biedl_syndrome_6|not_provided|MKKS-related_disorder|Syndromic_inherited_retinal_disease|Inborn_genetic_diseases|Nephronophthisis|Retinal_dystrophy": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|not_provided|not_specified|MKKS-related_disorder|Bardet-Biedl_syndrome_6|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|MKKS-related_disorder|Inborn_genetic_diseases": 1,
    "Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided|MKKS-related_disorder": 1,
    "Inborn_genetic_diseases|MKKS-related_disorder|Bardet-Biedl_syndrome_6|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome": 1,
    "not_specified|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|Bardet-Biedl_syndrome|not_provided": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|not_provided|Bardet-Biedl_syndrome_6": 1,
    "MKKS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|MKKS-related_disorder|not_specified|Bardet-Biedl_syndrome|McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6": 1,
    "McKusick-Kaufman_syndrome|Bardet-Biedl_syndrome_6|not_provided": 2,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease": 42,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided": 6,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease": 3,
    "Arteriohepatic_dysplasia|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Arteriohepatic_dysplasia": 7,
    "Arteriohepatic_dysplasia|not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "JAG1-related_disorder": 48,
    "JAG1-related_disorder|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|not_provided|JAG1-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease": 3,
    "Cardiovascular_phenotype|JAG1-related_disorder": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 70,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation": 850,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 69,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder": 12,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 35,
    "Cardiovascular_phenotype|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 6,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 33,
    "Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Cardiovascular_phenotype": 6,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Isolated_Nonsyndromic_Congenital_Heart_Disease": 2,
    "Cardiovascular_phenotype|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|not_provided": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 8,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|not_provided": 1,
    "Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided|JAG1-related_disorder|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided": 3,
    "Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 5,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Isolated_Nonsyndromic_Congenital_Heart_Disease": 2,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_specified|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Scoliosis|Pes_planus|Aortic_dilatation": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 6,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Cardiovascular_phenotype|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 3,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided|Conotruncal_heart_malformations": 1,
    "Tetralogy_of_Fallot|not_specified|Isolated_Nonsyndromic_Congenital_Heart_Disease|JAG1-related_disorder|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|JAG1-related_disorder": 3,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|JAG1-related_disorder": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Isolated_Nonsyndromic_Congenital_Heart_Disease": 2,
    "JAG1-related_disorder|Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|JAG1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Cardiovascular_phenotype": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified": 1,
    "Retinal_dystrophy|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 10,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype": 5,
    "not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|JAG1-related_disorder|Cardiovascular_phenotype": 1,
    "Retinal_dystrophy|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|not_specified|not_provided|JAG1-related_disorder": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Cardiovascular_phenotype|not_provided": 1,
    "JAG1-related_disorder|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype": 3,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 1,
    "Arteriohepatic_dysplasia": 2,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 3,
    "not_specified|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 2,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 3,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation": 10,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 38,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Cardiovascular_phenotype": 2,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|See_cases": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|JAG1-related_disorder": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot": 1,
    "not_provided|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Hepatic_Ductular_Hypoplasia": 2,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "not_provided|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 13,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided|Cardiovascular_phenotype": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Cardiovascular_phenotype": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "Cardiovascular_phenotype|not_specified|Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Cardiovascular_phenotype": 5,
    "not_provided|Atypical_coarctation_of_aorta|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 5,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 2,
    "not_provided|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 5,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|not_provided|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|JAG1-related_disorder": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|Arteriohepatic_dysplasia": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Cardiovascular_phenotype|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|not_specified": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|not_provided": 1,
    "not_specified|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Cardiovascular_phenotype|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|JAG1-related_disorder": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Retinal_dystrophy": 1,
    "Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|not_provided|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|not_provided": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided|Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|JAG1-related_disorder": 1,
    "JAG1-related_disorder|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 3,
    "not_provided|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 2,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|JAG1-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Heart|_malformation_of|Arteriohepatic_dysplasia|JAG1-related_disorder|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided|Arteriohepatic_dysplasia": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "JAG1-related_disorder|not_provided|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 2,
    "not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_provided": 3,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder": 1,
    "JAG1-related_disorder|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|JAG1-related_disorder": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|JAG1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype": 1,
    "JAG1-related_disorder|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided": 1,
    "not_specified|JAG1-related_disorder|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|not_specified|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot": 1,
    "not_provided|Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 2,
    "Cardiovascular_phenotype|not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided|JAG1-related_disorder|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease": 2,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder": 4,
    "JAG1-related_disorder|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided": 2,
    "not_provided|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_specified|Cardiovascular_phenotype": 2,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Arteriohepatic_dysplasia|JAG1-related_disorder|not_provided": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|Cardiovascular_phenotype": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|JAG1-related_disorder|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|not_specified|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|not_provided": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 1,
    "JAG1-related_disorder|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_provided|JAG1-related_disorder": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Inborn_genetic_diseases": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype|Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_specified|not_provided": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Tetralogy_of_Fallot": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot": 1,
    "Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "JAG1-related_disorder|not_specified|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided": 1,
    "JAG1-related_disorder|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Cardiovascular_phenotype|Isolated_Nonsyndromic_Congenital_Heart_Disease|JAG1-related_disorder|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_specified|not_provided": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|not_provided": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH": 1,
    "not_provided|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|not_provided": 1,
    "not_specified|not_provided|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "JAG1-related_disorder|not_specified|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_provided": 1,
    "JAG1-related_disorder|Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "JAG1-related_disorder|not_provided|Atypical_coarctation_of_aorta|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "not_specified|Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_specified|not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Tetralogy_of_Fallot|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "not_provided|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation": 2,
    "JAG1-related_disorder|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease|Cardiovascular_phenotype": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified|not_provided": 1,
    "not_provided|Isolated_Nonsyndromic_Congenital_Heart_Disease|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|not_specified|Cardiovascular_phenotype": 1,
    "JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_specified": 1,
    "not_provided|Arteriohepatic_dysplasia": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Alagille_syndrome_due_to_a_JAG1_point_mutation|Isolated_Nonsyndromic_Congenital_Heart_Disease": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|JAG1-related_disorder|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Retinal_dystrophy|Alagille_syndrome_due_to_a_JAG1_point_mutation": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_specified": 1,
    "Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Alagille_syndrome_due_to_a_JAG1_point_mutation|not_provided": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "Tetralogy_of_Fallot|Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|JAG1-related_disorder|Alagille_syndrome_due_to_a_JAG1_point_mutation|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon": 1,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Deafness|_congenital_heart_defects|_and_posterior_embryotoxon|Tetralogy_of_Fallot|Charcot-Marie-Tooth_disease|_axonal|_Type_2HH|Isolated_Nonsyndromic_Congenital_Heart_Disease|not_provided": 1,
    "Isolated_Nonsyndromic_Congenital_Heart_Disease|Arteriohepatic_dysplasia|not_provided": 2,
    "Peripheral_neuropathy|Sensory_neuropathy": 1,
    "ISM1-related_disorder": 15,
    "not_specified|ISM1-related_disorder": 1,
    "TASP1-related_disorder": 13,
    "Suleiman-El-Hattab_syndrome": 8,
    "Suleiman-El-Hattab_syndrome|Inborn_genetic_diseases": 1,
    "Abnormal_facial_shape|Global_developmental_delay|Happy_demeanor|Suleiman-El-Hattab_syndrome": 1,
    "not_provided|TASP1-related_disorder|Inborn_genetic_diseases": 1,
    "NDUFAF5-related_disorder|not_provided": 2,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_16": 22,
    "not_provided|NDUFAF5-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16": 38,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided": 2,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|not_provided|Leigh_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Inborn_genetic_diseases": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided": 5,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Mitochondrial_complex_I_deficiency|not_provided|not_specified": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided|Mitochondrial_complex_I_deficiency": 3,
    "Mitochondrial_complex_I_deficiency|NDUFAF5-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Leigh_syndrome|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Leber_plus_disease": 1,
    "Inborn_genetic_diseases|NDUFAF5-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_nuclear_type_16": 1,
    "Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_specified|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Leigh_syndrome|NDUFAF5-related_disorder|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Leigh_syndrome|not_specified|not_provided": 1,
    "Leigh_syndrome|NDUFAF5-related_disorder|not_provided": 1,
    "not_specified|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency|_nuclear_type_16": 1,
    "Mitochondrial_complex_I_deficiency|not_specified|not_provided": 2,
    "not_provided|not_specified|NDUFAF5-related_disorder": 1,
    "Leigh_syndrome|not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_16": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Inborn_genetic_diseases|Leigh_syndrome|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_16|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|NDUFAF5-related_disorder|not_provided|Mitochondrial_complex_I_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_I_deficiency|NDUFAF5-related_disorder": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided": 1,
    "not_specified|Mitochondrial_complex_I_deficiency|_nuclear_type_16": 1,
    "Inborn_genetic_diseases|Mitochondrial_complex_I_deficiency|_nuclear_type_16|not_provided|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_16|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_1|Mitochondrial_complex_I_deficiency|_nuclear_type_16|Leber_plus_disease|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_16|Mitochondrial_complex_I_deficiency": 1,
    "MACROD2-related_disorder|not_provided": 1,
    "MACROD2-related_disorder": 8,
    "Hypogonadotropic_hypogonadism_21_with_or_without_anosmia": 4,
    "FLRT3-related_disorder|not_provided|not_specified": 1,
    "FLRT3-related_disorder": 1,
    "not_provided|Hypogonadotropic_hypogonadism_21_with_or_without_anosmia": 1,
    "Hypogonadotropic_hypogonadism_21_with_or_without_anosmia|not_provided": 1,
    "not_provided|FLRT3-related_disorder": 2,
    "not_specified|FLRT3-related_disorder": 1,
    "HYPOGONADOTROPIC_HYPOGONADISM_21_WITH_ANOSMIA|_SUSCEPTIBILITY_TO": 3,
    "not_provided|MACROD2-related_disorder": 1,
    "KIF16B-related_Intellectual_Disability|not_specified": 1,
    "OTOR-related_disorder": 2,
    "Cataract_33|Congenital_ocular_coloboma": 1,
    "not_provided|Cataract_33": 4,
    "Cataract_33": 48,
    "Cataract_33|not_provided": 7,
    "Inborn_genetic_diseases|Cataract_33": 5,
    "Cataract_33|not_specified|not_provided": 3,
    "Cataract_33|not_provided|BFSP1-related_disorder": 2,
    "Cataract_33|BFSP1-related_disorder": 4,
    "Cataract_33|not_provided|not_specified": 2,
    "BFSP1-related_disorder|Cataract_33": 1,
    "not_provided|Cataract_33|not_specified": 1,
    "Cataract_33|Inborn_genetic_diseases": 1,
    "Cataract_33|Inborn_genetic_diseases|not_provided": 1,
    "BFSP1-related_disorder": 8,
    "BFSP1-related_disorder|not_provided|Cataract_33": 1,
    "Cataract_33|BFSP1-related_disorder|not_provided": 1,
    "not_provided|BFSP1-related_disorder|Cataract_33": 1,
    "Inborn_genetic_diseases|Cataract_33|BFSP1-related_disorder|not_provided": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_11|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_11|not_provided": 3,
    "MGME1-related_disorder|not_specified|not_provided": 1,
    "not_provided|MGME1-related_disorder": 4,
    "Mitochondrial_DNA_depletion_syndrome_11": 8,
    "Mitochondrial_DNA_depletion_syndrome_11|Inborn_genetic_diseases": 1,
    "MGME1-related_disorder|not_provided": 3,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_11|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_11": 1,
    "OVOL2-related_disorder|not_specified|not_provided": 1,
    "OVOL2-related_disorder": 4,
    "Posterior_polymorphous_corneal_dystrophy_1|not_provided": 2,
    "Posterior_polymorphous_corneal_dystrophy_1|not_specified": 1,
    "PET117-related_disorder": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_19": 1,
    "Immunodeficiency_101_(varicella_zoster_virus-specific)": 2,
    "SEC23B-related_disorder|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_provided": 4,
    "Congenital_dyserythropoietic_anemia|not_provided": 2,
    "Congenital_dyserythropoietic_anemia|_type_II": 29,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II": 183,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7": 234,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7": 15,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|SEC23B-related_disorder": 1,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|not_specified|not_provided": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_provided": 26,
    "SEC23B-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|Inborn_genetic_diseases": 3,
    "SEC23B-related_disorder|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II": 3,
    "not_provided|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II": 7,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|not_provided": 6,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|not_specified": 1,
    "SEC23B-related_disorder": 4,
    "SEC23B-related_disorder|Cowden_syndrome_7": 1,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_II": 2,
    "not_provided|Cowden_syndrome_7|Inborn_genetic_diseases": 1,
    "SEC23B-related_disorder|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_provided|See_cases": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_specified|not_provided": 7,
    "Inborn_genetic_diseases|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II": 3,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|SEC23B-related_disorder|not_provided": 2,
    "See_cases|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|not_provided": 1,
    "SEC23B-related_disorder|not_provided|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7": 1,
    "Cowden_syndrome_7": 4,
    "not_provided|Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7": 1,
    "Cowden_syndrome_7|not_provided|Congenital_dyserythropoietic_anemia|_type_II": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_provided|not_specified": 2,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|SEC23B-related_disorder": 2,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_II|not_specified|Cowden_syndrome_7": 2,
    "not_specified|not_provided|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|not_provided|Cowden_syndrome_7": 3,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia": 1,
    "not_provided|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|SEC23B-related_disorder": 1,
    "not_specified|Hereditary_ataxia": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|SEC23B-related_disorder": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_specified": 2,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_specified|SEC23B-related_disorder": 1,
    "not_specified|Congenital_dyserythropoietic_anemia|_type_II": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_specified|SEC23B-related_disorder": 1,
    "not_provided|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_specified": 2,
    "SEC23B-related_disorder|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|SEC23B-related_disorder|not_provided": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|SEC23B-related_disorder|Cowden_syndrome_7|not_provided": 1,
    "SEC23B-related_disorder|not_provided|Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|SEC23B-related_disorder": 1,
    "Cowden_syndrome_7|not_provided": 1,
    "Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7": 1,
    "Cowden_syndrome_7|Congenital_dyserythropoietic_anemia|_type_II|not_provided|SEC23B-related_disorder": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|not_specified": 1,
    "Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_II|Cowden_syndrome_7|not_provided": 1,
    "Congenital_dyserythropoietic_anemia|_type_II|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Congenital_dyserythropoietic_anemia|_type_II": 1,
    "Congenital_dyserythropoietic_anemia|not_specified": 1,
    "RIN2-related_disorder": 9,
    "not_provided|not_specified|RIN2-related_disorder": 2,
    "RIN2-related_disorder|not_provided": 10,
    "not_provided|Inborn_genetic_diseases|RIN2_syndrome": 3,
    "not_specified|not_provided|RIN2_syndrome": 3,
    "RIN2_syndrome|not_provided": 4,
    "RIN2_syndrome": 8,
    "not_provided|RIN2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|RIN2_syndrome": 2,
    "Inborn_genetic_diseases|RIN2_syndrome|not_provided|RIN2-related_disorder": 1,
    "not_provided|RIN2-related_disorder": 7,
    "not_specified|RIN2-related_disorder|not_provided": 1,
    "not_specified|RIN2_syndrome|not_provided|RIN2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|RIN2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "RIN2_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|RIN2-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|RIN2-related_disorder|not_specified|not_provided": 1,
    "RIN2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|RIN2-related_disorder|Inborn_genetic_diseases|not_provided|RIN2_syndrome": 1,
    "not_provided|not_specified|RIN2_syndrome": 1,
    "not_specified|not_provided|RIN2-related_disorder": 1,
    "Inborn_genetic_diseases|RIN2-related_disorder|not_provided": 1,
    "RIN2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|RIN2_syndrome": 1,
    "RIN2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|RIN2-related_disorder": 1,
    "Intellectual_developmental_disorder|_autosomal_recessive_73": 2,
    "Spermatogenic_failure_84": 7,
    "KIZ-related_disorder": 3,
    "Retinitis_pigmentosa_69|not_provided": 4,
    "Retinal_dystrophy|Retinitis_pigmentosa_69": 1,
    "Retinitis_pigmentosa_69": 1,
    "not_provided|KIZ-related_disorder": 7,
    "Retinitis_pigmentosa_69|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "KIZ-related_disorder|not_provided": 2,
    "KIZ-related_disorder|Retinitis_pigmentosa_69|Retinal_dystrophy|not_provided|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_69": 1,
    "KIZ-related_retinopathy": 1,
    "KIZ-related_disorder|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|not_provided|KIZ-related_disorder": 1,
    "KIZ-related_retinopathy|not_provided": 1,
    "KIZ-related_disorder|Retinal_dystrophy": 1,
    "KIZ-related_disorder|not_provided|Retinitis_pigmentosa_69": 1,
    "NKX2-2-related_disorder": 3,
    "NKX2-2-related_disorder|not_provided": 2,
    "not_provided|PAX1-related_disorder": 10,
    "PAX1-related_disorder|not_provided": 2,
    "Otofaciocervical_syndrome_2|not_provided": 5,
    "Otofaciocervical_syndrome_2": 6,
    "PAX1-related_disorder": 2,
    "not_provided|Otofaciocervical_syndrome_2": 1,
    "not_provided|Otofaciocervical_syndrome_2|Inborn_genetic_diseases": 1,
    "Otofaciocervical_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Otofaciocervical_syndrome_2": 1,
    "not_provided|Inborn_genetic_diseases|Otofaciocervical_syndrome_2": 2,
    "not_provided|not_specified|Otofaciocervical_syndrome_2": 1,
    "not_specified|not_provided|FOXA2-related_disorder": 1,
    "FOXA2-related_disorder": 4,
    "FOXA2-related_disorder|not_provided": 2,
    "not_provided|FOXA2-related_disorder": 4,
    "not_provided|not_specified|FOXA2-related_disorder": 2,
    "Non-acquired_combined_pituitary_hormone_deficiency": 1,
    "Congenital_syndromic_hypopituitarism": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 45,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided": 10,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 4,
    "Thrombomodulin-related_bleeding_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 2,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided|Thrombomodulin-related_bleeding_disorder": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 3,
    "Thrombomodulin-related_bleeding_disorder": 66,
    "Inborn_genetic_diseases|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided": 2,
    "Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 37,
    "not_provided|Thrombomodulin-related_bleeding_disorder": 13,
    "Inborn_genetic_diseases|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 1,
    "not_provided|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 10,
    "Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided": 10,
    "Thrombomodulin-related_bleeding_disorder|Thrombocytopenia|Abnormal_bleeding": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|not_provided": 12,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 7,
    "THBD-related_disorder|not_provided": 2,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Inborn_genetic_diseases": 1,
    "Thrombomodulin-related_bleeding_disorder|not_provided": 7,
    "Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_specified|not_provided": 1,
    "THBD-related_disorder": 3,
    "THBD-related_disorder|Thrombocytopenia|Abnormal_bleeding|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Thrombomodulin-related_bleeding_disorder": 1,
    "Thrombomodulin-related_bleeding_disorder|Abnormal_bleeding": 2,
    "THBD-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 1,
    "Kidney_disorder|THBD-related_disorder|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 1,
    "Thrombomodulin-related_bleeding_disorder|not_provided|Abnormal_bleeding": 1,
    "THBD-related_disorder|Variant_of_unknown_significance|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided|Atypical_hemolytic-uremic_syndrome|Thrombomodulin-related_bleeding_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 1,
    "Thrombomodulin-related_bleeding_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Inborn_genetic_diseases": 1,
    "THBD-related_disorder|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Inborn_genetic_diseases|not_provided": 1,
    "Thrombomodulin-related_bleeding_disorder|Abnormal_bleeding|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 1,
    "THBD-related_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|not_specified|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "not_provided|Thrombomodulin-related_bleeding_disorder|not_specified|Atypical_hemolytic-uremic_syndrome": 1,
    "THBD-related_disorder|Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|not_provided": 1,
    "THBD-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|Inborn_genetic_diseases": 1,
    "Thrombomodulin-related_bleeding_disorder|not_provided|not_specified": 1,
    "Atypical_hemolytic-uremic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Thrombomodulin-related_bleeding_disorder|Thrombocytopenia|Abnormal_bleeding": 1,
    "Inborn_genetic_diseases|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|Thrombocytopenia|Abnormal_bleeding|not_provided": 1,
    "Inborn_genetic_diseases|Thrombomodulin-related_bleeding_disorder|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly": 1,
    "not_provided|Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Thrombomodulin-related_bleeding_disorder": 1,
    "not_provided|THBD-related_disorder": 2,
    "Inborn_genetic_diseases|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|not_provided": 2,
    "not_provided|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombocytopenia|Abnormal_bleeding": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|THBD-related_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Abnormal_thrombosis": 1,
    "THBD-related_disorder|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 1,
    "not_provided|Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Inborn_genetic_diseases": 1,
    "Thrombomodulin-related_bleeding_disorder|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|not_provided|Inborn_genetic_diseases": 1,
    "THBD-related_disorder|not_specified|not_provided|Atypical_hemolytic-uremic_syndrome_with_thrombomodulin_anomaly|Thrombomodulin-related_bleeding_disorder": 1,
    "CD93-related_disorder": 11,
    "not_specified|CD93-related_disorder": 1,
    "GZF1-related_disorder|not_provided": 7,
    "GZF1-related_disorder": 1,
    "Joint_laxity|_short_stature|_and_myopia": 10,
    "GZF1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Joint_laxity|_short_stature|_and_myopia": 1,
    "Joint_laxity|_short_stature|_and_myopia|not_provided": 3,
    "not_provided|GZF1-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy-107": 4,
    "Developmental_and_epileptic_encephalopathy-107|Developmental_and_epileptic_encephalopathy|_1": 1,
    "NAPB-related_disorder": 1,
    "not_provided|NAPB-related_disorder": 1,
    "Hereditary_cerebral_amyloid_angiopathy|_Icelandic_type|not_provided": 1,
    "CST3-related_Leukodystrophy|LEUKODYSTROPHY|_ADULT-ONSET|_AUTOSOMAL_DOMINANT|_WITHOUT_AMYLOID_ANGIOPATHY": 1,
    "not_provided|CST3-related_Leukodystrophy|LEUKODYSTROPHY|_ADULT-ONSET|_AUTOSOMAL_DOMINANT|_WITHOUT_AMYLOID_ANGIOPATHY": 1,
    "LEUKODYSTROPHY|_ADULT-ONSET|_AUTOSOMAL_DOMINANT|_WITHOUT_AMYLOID_ANGIOPATHY|not_provided|CST3-related_Leukodystrophy|Hereditary_cerebral_amyloid_angiopathy|_Icelandic_type": 1,
    "Hereditary_cerebral_amyloid_angiopathy|_Icelandic_type": 4,
    "Age_related_macular_degeneration_11|Hereditary_cerebral_amyloid_angiopathy|_Icelandic_type|not_provided|not_specified": 1,
    "not_provided|Posterior_polymorphous_corneal_dystrophy": 4,
    "Posterior_polymorphous_corneal_dystrophy|not_provided": 13,
    "not_provided|Keratoconus_1|Craniofacial_anomalies_and_anterior_segment_dysgenesis_syndrome": 2,
    "VSX1-related_disorder": 3,
    "Craniofacial_anomalies_and_anterior_segment_dysgenesis_syndrome|not_specified": 1,
    "Posterior_polymorphous_corneal_dystrophy|Keratoconus_1|Craniofacial_anomalies_and_anterior_segment_dysgenesis_syndrome|not_provided": 1,
    "VSX1-related_disorder|Posterior_polymorphous_corneal_dystrophy|Keratoconus_1|not_provided": 1,
    "Keratoconus_1|Craniofacial_anomalies_and_anterior_segment_dysgenesis_syndrome": 2,
    "Posterior_polymorphous_corneal_dystrophy|not_provided|not_specified": 1,
    "Posterior_polymorphous_corneal_dystrophy|Keratoconus_1": 2,
    "Posterior_polymorphous_corneal_dystrophy|not_specified|not_provided|Posterior_polymorphous_corneal_dystrophy_1": 1,
    "VSX1-related_disorder|Posterior_polymorphous_corneal_dystrophy|not_provided": 2,
    "Posterior_polymorphous_corneal_dystrophy|not_specified": 1,
    "Craniofacial_anomalies_and_anterior_segment_dysgenesis_syndrome": 1,
    "Inborn_genetic_diseases|Posterior_polymorphous_corneal_dystrophy": 3,
    "Keratoconus|not_specified|not_provided|VSX1-related_disorder|Posterior_polymorphous_corneal_dystrophy": 1,
    "Inborn_genetic_diseases|VSX1-related_disorder": 1,
    "VSX1-related_disorder|Inborn_genetic_diseases|Posterior_polymorphous_corneal_dystrophy|not_provided": 1,
    "VSX1-related_disorder|Posterior_polymorphous_corneal_dystrophy|Keratoconus_1": 1,
    "not_specified|Posterior_polymorphous_corneal_dystrophy|not_provided": 1,
    "ABHD12-related_disorder": 5,
    "PHARC_syndrome": 29,
    "PHARC_syndrome|not_provided": 24,
    "not_provided|PHARC_syndrome": 16,
    "not_provided|PHARC_syndrome|not_specified": 2,
    "not_provided|ABHD12-related_disorder": 4,
    "ABHD12-related_disorder|not_specified|not_provided": 1,
    "not_specified|ABHD12-related_disorder|not_provided": 1,
    "PHARC_syndrome|not_provided|not_specified": 1,
    "ABHD12-related_disorder|not_provided|PHARC_syndrome": 1,
    "not_provided|Syndromic_retinitis_pigmentosa": 1,
    "ABHD12-related_disorder|not_provided": 2,
    "PHARC_syndrome|not_specified|not_provided": 2,
    "not_provided|ABHD12-related_disorder|not_specified": 1,
    "not_provided|PHARC_syndrome|ABHD12-related_disorder|Retinal_dystrophy": 1,
    "ABHD12-related_disorder|Retinal_dystrophy": 1,
    "ABHD12-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "PHARC_syndrome|Retinal_dystrophy": 1,
    "Cone_dystrophy|PHARC_syndrome": 1,
    "Inborn_genetic_diseases|PHARC_syndrome": 1,
    "PHARC_syndrome|not_specified|not_provided|ABHD12-related_disorder": 1,
    "PHARC_syndrome|Retinal_dystrophy|not_provided": 1,
    "ABHD12-related_disorder|not_provided|Optic_atrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|PHARC_syndrome|Retinal_dystrophy|not_provided": 1,
    "Combined_immunodeficiency_due_to_GINS1_deficiency": 3,
    "Combined_immunodeficiency_due_to_GINS1_deficiency|not_provided": 1,
    "not_provided|GINS1-related_disorder": 1,
    "Combined_immunodeficiency_due_to_GINS1_deficiency|GINS1-related_disorder|not_provided": 1,
    "GINS1-related_disorder|not_provided": 1,
    "not_provided|Combined_immunodeficiency_due_to_GINS1_deficiency": 1,
    "not_specified|not_provided|Combined_immunodeficiency_due_to_GINS1_deficiency": 1,
    "GINS1-related_disorder": 1,
    "Combined_immunodeficiency_due_to_GINS1_deficiency|not_specified|not_provided": 1,
    "NINL-related_disorder": 14,
    "not_specified|NINL-related_disorder": 2,
    "NINL-related_disorder|not_provided": 1,
    "not_provided|Pancreatic_insufficiency-anemia-hyperostosis_syndrome": 3,
    "Pancreatic_insufficiency-anemia-hyperostosis_syndrome|not_provided": 4,
    "not_specified|not_provided|COX4I2-related_disorder": 1,
    "COX4I2-related_disorder": 2,
    "Pancreatic_insufficiency-anemia-hyperostosis_syndrome": 1,
    "MYLK2-related_disorder|Cardiomyopathy|Long_QT_syndrome|Ventricular_tachycardia|not_specified|not_provided|Hypertrophic_cardiomyopathy_1": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1": 11,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 3,
    "not_provided|Hypertrophic_cardiomyopathy_1|not_specified": 8,
    "See_cases|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "MYLK2-related_disorder": 3,
    "not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1": 1,
    "not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "not_specified|Cardiomyopathy|_hypertrophic|_midventricular|_digenic|not_provided|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|not_specified|Hypertrophic_cardiomyopathy|Cardiomyopathy": 1,
    "MYLK2-related_disorder|not_provided|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|_hypertrophic|_midventricular|_digenic": 1,
    "not_specified|Hypertrophic_cardiomyopathy_1|not_provided": 6,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Sudden_unexplained_death": 1,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 2,
    "MYLK2-related_disorder|not_specified": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder|Cardiomyopathy|not_provided|not_specified": 1,
    "Cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|not_specified": 2,
    "not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "MYLK2-related_disorder|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 2,
    "MYLK2-related_disorder|not_specified|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_1|not_specified|not_provided": 4,
    "Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_provided|not_specified": 2,
    "MYLK2-related_disorder|Hypertrophic_cardiomyopathy_1|not_provided|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy|MYLK2-related_disorder|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|Fabry_disease": 2,
    "Dilated_cardiomyopathy_1KK|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy|not_specified": 1,
    "Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder|not_specified|Cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|not_specified": 3,
    "not_specified|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 2,
    "MYLK2-related_disorder|Hypertrophic_cardiomyopathy_1": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_1|not_specified|Ventricular_tachycardia": 1,
    "Hypertrophic_cardiomyopathy_1|not_specified|not_provided|Cardiomyopathy": 1,
    "not_specified|MYLK2-related_disorder|Cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_provided": 1,
    "not_specified|Hypertrophic_cardiomyopathy_1|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder": 1,
    "Cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_1": 1,
    "Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder|not_specified|not_provided": 1,
    "Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder": 2,
    "Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder|not_specified": 1,
    "not_specified|MYLK2-related_disorder|not_provided|Hypertrophic_cardiomyopathy_1|Cardiomyopathy": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_1|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy_1": 1,
    "not_provided|MYLK2-related_disorder|See_cases|Hypertrophic_cardiomyopathy_1": 1,
    "MYLK2-related_disorder|Hypertrophic_cardiomyopathy_1|not_specified|Cardiomyopathy": 1,
    "Cardiomyopathy|Hypertrophic_cardiomyopathy_1|not_specified": 1,
    "not_provided|Hypertrophic_cardiomyopathy_1|MYLK2-related_disorder": 1,
    "HCK-related_condition": 3,
    "Autoinflammation_with_pulmonary_and_cutaneous_vasculitis": 1,
    "TM9SF4-related_disorder": 2,
    "Dowling-Degos_disease_2": 57,
    "POFUT1-related_disorder|Dowling-Degos_disease_2|not_provided": 2,
    "Dowling-Degos_disease_2|Inborn_genetic_diseases": 2,
    "POFUT1-related_disorder": 3,
    "not_provided|Dowling-Degos_disease_2": 4,
    "Dowling-Degos_disease_2|not_provided": 5,
    "Inborn_genetic_diseases|Dowling-Degos_disease_2": 2,
    "Dowling-Degos_disease_2|POFUT1-related_disorder": 1,
    "POFUT1-related_disorder|not_provided|Dowling-Degos_disease_2": 1,
    "Dowling-Degos_disease_2|not_provided|POFUT1-related_disorder": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_89": 1,
    "Optic_atrophy|not_specified": 1,
    "KIF3B-related_disorder": 2,
    "Retinitis_pigmentosa_89": 4,
    "Oligospermia": 2,
    "not_provided|Bohring-Opitz_syndrome": 11,
    "ASXL1-related_disorder": 13,
    "not_provided|Bohring-Opitz_syndrome|Myelodysplastic_syndrome": 2,
    "Bohring-Opitz_syndrome": 68,
    "not_provided|ASXL1-related_disorder": 3,
    "ASXL1-related_disorder|Inborn_genetic_diseases": 2,
    "Bohring-Opitz_syndrome|Myelodysplastic_syndrome|not_provided|not_specified": 1,
    "Bohring-Opitz_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "ASXL1-related_disorder|not_provided": 7,
    "not_specified|not_provided|Intellectual_disability|Inborn_genetic_diseases": 1,
    "not_specified|Myelodysplastic_syndrome|Bohring-Opitz_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|ASXL1-related_disorder": 4,
    "not_specified|Bohring-Opitz_syndrome": 1,
    "Bohring-Opitz_syndrome|ASXL1-related_disorder|not_provided": 2,
    "Bohring-Opitz_syndrome|Myelodysplastic_syndrome|not_provided": 1,
    "Bohring-Opitz_syndrome|not_provided": 14,
    "Moderate_global_developmental_delay|Hypertonia|Seizure|Delayed_speech_and_language_development|Global_developmental_delay|Floppy_infant|not_provided": 1,
    "Inborn_genetic_diseases|ASXL1-related_disorder": 3,
    "not_provided|ASXL1-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|ASXL1-related_disorder": 4,
    "dystrophia|Developmental_delay|Global_developmental_delay|Small_for_gestational_age|Delayed_speech_and_language_development|Prominent_metopic_ridge|Glabellar_hemangioma|Intellectual_disability|_severe|Hypertrichosis|Abnormal_corpus_callosum_morphology|Feeding_difficulties|Delayed_gross_motor_development|Myelodysplastic_syndrome|not_provided|Bohring-Opitz_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Bohring-Opitz_syndrome": 7,
    "not_specified|not_provided|Bohring-Opitz_syndrome|ASXL1-related_disorder": 1,
    "ASXL1-related_disorder|not_provided|Bohring-Opitz_syndrome": 4,
    "Inborn_genetic_diseases|not_provided|Bohring-Opitz_syndrome": 6,
    "Inborn_genetic_diseases|Bohring-Opitz_syndrome": 5,
    "Juvenile_myelomonocytic_leukemia|Cafe-au-lait_spot|not_provided|Bohring-Opitz_syndrome": 1,
    "Atypical_chronic_myeloid_leukemia|_BCR-ABL1_negative": 1,
    "ASXL1-related_disorder|not_provided|Bohring-Opitz_syndrome|Inborn_genetic_diseases": 3,
    "Juvenile_myelomonocytic_leukemia|Myelodysplastic_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|ASXL1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Bohring-Opitz_syndrome|not_provided|ASXL1-related_disorder": 1,
    "Bohring-Opitz_syndrome|ASXL1-related_disorder|not_provided|Abnormal_brain_morphology": 1,
    "not_specified|not_provided|Bohring-Opitz_syndrome": 9,
    "Bohring-Opitz_syndrome|Inborn_genetic_diseases": 1,
    "Bohring-Opitz_syndrome|Myelodysplastic_syndrome": 3,
    "Bohring-Opitz_syndrome|ASXL1-related_disorder|not_provided|Myelodysplastic_syndrome": 1,
    "Myelodysplastic_syndrome|Bohring-Opitz_syndrome|not_provided": 2,
    "Myelodysplasia": 1,
    "not_provided|Bohring-Opitz_syndrome|ASXL1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Bohring-Opitz_syndrome|ASXL1-related_disorder": 3,
    "Inborn_genetic_diseases|Bohring-Opitz_syndrome|not_provided": 2,
    "not_provided|not_specified|Bohring-Opitz_syndrome": 1,
    "Bohring-Opitz_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|not_provided|Bohring-Opitz_syndrome": 1,
    "ASXL1-related_disorder|Bohring-Opitz_syndrome|Myelodysplastic_syndrome|not_specified|not_provided": 1,
    "Bohring-Opitz_syndrome|Intellectual_disability|not_provided": 1,
    "not_specified|Bohring-Opitz_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Bohring-Opitz_syndrome": 1,
    "Bohring-Opitz_syndrome|not_specified|not_provided": 2,
    "Bohring-Opitz_syndrome|Myelodysplastic_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Bohring-Opitz_syndrome|not_provided|not_specified": 1,
    "ASXL1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Myelodysplastic_syndrome|Bohring-Opitz_syndrome|not_provided": 1,
    "ASXL1-related_disorder|not_specified|not_provided|Bohring-Opitz_syndrome": 1,
    "Hereditary_cancer|not_provided|Inborn_genetic_diseases": 1,
    "Rubinstein_Taybi_like_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "ASXL1-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "ASXL1-related_disorder|Bohring-Opitz_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 637,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 61,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_provided": 4,
    "DNMT3B-related_disorder": 3,
    "Inborn_genetic_diseases|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 15,
    "DNMT3B-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_provided": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Inborn_genetic_diseases": 20,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_provided": 11,
    "DNMT3B-related_disorder|Inborn_genetic_diseases|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_specified|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_provided": 1,
    "not_provided|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 10,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_provided": 5,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Inborn_genetic_diseases|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "DNMT3B-related_disorder|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 9,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Inborn_genetic_diseases|not_provided": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 14,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 16,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 3,
    "Inborn_genetic_diseases|DNMT3B-related_disorder|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "DNMT3B-related_disorder|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "DNMT3B-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Facioscapulohumeral_muscular_dystrophy_4|_digenic|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_specified": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_specified|DNMT3B-related_disorder|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Facioscapulohumeral_muscular_dystrophy_4|_digenic|not_provided": 1,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|DNMT3B-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_provided|See_cases": 1,
    "not_provided|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Kabuki_syndrome_1|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_specified|not_provided": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Facioscapulohumeral_muscular_dystrophy_4|_digenic|Inborn_genetic_diseases|not_provided": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_specified|not_provided": 3,
    "DNMT3B-related_disorder|not_specified|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|DNMT3B-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Inborn_genetic_diseases|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "not_specified|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_provided|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Inborn_genetic_diseases|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_provided": 2,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Facioscapulohumeral_muscular_dystrophy_4|_digenic": 2,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Facioscapulohumeral_muscular_dystrophy_4|_digenic|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Facioscapulohumeral_muscular_dystrophy_4|_digenic": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|DNMT3B-related_disorder|not_provided": 1,
    "Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_specified|not_provided": 2,
    "Facioscapulohumeral_muscular_dystrophy_4|_digenic": 1,
    "Inborn_genetic_diseases|not_provided|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_specified": 2,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|DNMT3B-related_disorder|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|not_provided": 2,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|DNMT3B-related_disorder|not_specified|not_provided": 1,
    "Facioscapulohumeral_muscular_dystrophy_4|_digenic|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_provided|Inborn_genetic_diseases": 1,
    "Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|Facioscapulohumeral_muscular_dystrophy_4|_digenic": 1,
    "DNMT3B-related_disorder|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "not_specified|Facioscapulohumeral_muscular_dystrophy_4|_digenic|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "Inborn_genetic_diseases|Centromeric_instability_of_chromosomes_1|9_and_16_and_immunodeficiency|not_specified": 1,
    "not_provided|Immunodeficiency-centromeric_instability-facial_anomalies_syndrome_1": 1,
    "SUN5-related_disorder": 2,
    "Spermatogenic_failure_16|not_provided": 1,
    "Spermatogenic_failure_16": 5,
    "not_provided|Spermatogenic_failure_16": 1,
    "BPIFA3-related_disorder": 5,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_12|not_provided": 2,
    "Long_QT_syndrome_12|Congenital_long_QT_syndrome": 7,
    "not_provided|Long_QT_syndrome_12": 2,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome_12|not_provided|Congenital_long_QT_syndrome": 1,
    "not_provided|SNTA1-related_disorder": 1,
    "Long_QT_syndrome_12|Long_QT_syndrome": 5,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_12": 3,
    "Long_QT_syndrome_12|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 2,
    "Long_QT_syndrome_12|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome_12|Cardiovascular_phenotype|Long_QT_syndrome": 4,
    "Long_QT_syndrome_12|Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome_12|not_specified|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|not_specified|SNTA1-related_disorder|Long_QT_syndrome_12|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome_12|Long_QT_syndrome|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_12|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome_12|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_12|Cardiovascular_phenotype": 2,
    "not_specified|Long_QT_syndrome_12|Long_QT_syndrome": 1,
    "Long_QT_syndrome_12|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Long_QT_syndrome|Long_QT_syndrome_12": 2,
    "Cardiovascular_phenotype|not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_12|not_provided": 2,
    "Long_QT_syndrome_12|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_12|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_12": 4,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Long_QT_syndrome_12": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_12|Long_QT_syndrome|not_provided|Atrial_fibrillation": 1,
    "Long_QT_syndrome_12|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_12|Congenital_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|not_specified|Long_QT_syndrome_12|Wolff-Parkinson-White_pattern": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_12": 3,
    "Long_QT_syndrome_12|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome_12|not_provided|Cardiovascular_phenotype|Long_QT_syndrome": 2,
    "Long_QT_syndrome_12|Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|not_specified": 1,
    "not_provided|Long_QT_syndrome_12|Long_QT_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_12|Congenital_long_QT_syndrome|not_specified": 1,
    "Long_QT_syndrome_12|not_provided": 1,
    "Long_QT_syndrome|Long_QT_syndrome_12|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_12|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Brugada_syndrome|Long_QT_syndrome": 1,
    "not_specified|Long_QT_syndrome_12|not_provided|Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|not_specified|Cardiovascular_phenotype|not_provided|Long_QT_syndrome_12": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_12|not_provided|not_specified|Long_QT_syndrome": 1,
    "Long_QT_syndrome_1|SNTA1-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Long_QT_syndrome_12|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_12|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_12|Long_QT_syndrome": 3,
    "not_specified|Long_QT_syndrome|not_provided|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome|not_specified|not_provided|SNTA1-related_disorder|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome_12|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_12|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_12": 2,
    "Ventricular_fibrillation|_paroxysmal_familial|_type_1|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome_12|Long_QT_syndrome|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified": 1,
    "Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome|Long_QT_syndrome_12|Cardiovascular_phenotype|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_12|not_provided|Long_QT_syndrome|Congenital_long_QT_syndrome|not_specified": 1,
    "SNTA1-related_disorder|Cardiovascular_phenotype": 2,
    "not_provided|Long_QT_syndrome_1|Long_QT_syndrome|Long_QT_syndrome_12|Cardiovascular_phenotype": 1,
    "Sick_sinus_syndrome|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome|Cardiovascular_phenotype|SNTA1-related_disorder": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|not_specified|Long_QT_syndrome_12|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_12|Long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|SNTA1-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_provided|Long_QT_syndrome_12|not_specified": 1,
    "Long_QT_syndrome|SNTA1-related_disorder|Cardiovascular_phenotype": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome|SNTA1-related_disorder": 1,
    "Long_QT_syndrome_12|not_specified|SNTA1-related_disorder|not_provided|Ventricular_tachycardia|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Long_QT_syndrome|Long_QT_syndrome_12|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_12|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome_12|Cardiovascular_phenotype|Long_QT_syndrome|Congenital_long_QT_syndrome|not_provided": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_12": 1,
    "Long_QT_syndrome|not_provided|Long_QT_syndrome_12|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome|Long_QT_syndrome_12": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_12": 2,
    "not_provided|Long_QT_syndrome_12|Congenital_long_QT_syndrome": 1,
    "E2F1-related_disorder": 7,
    "E2F1-related_disorder|not_provided": 3,
    "ZNF341-related_disorder": 2,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided|not_specified": 2,
    "not_provided|ZNF341-related_disorder": 10,
    "ZNF341-related_disorder|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided": 1,
    "ZNF341-related_disorder|not_provided": 11,
    "not_provided|ZNF341-related_disorder|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive|not_provided|ZNF341-related_disorder|not_specified": 1,
    "not_specified|not_provided|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "ZNF341-related_disorder|not_provided|not_specified|Hyper-IgE_recurrent_infection_syndrome_3|_autosomal_recessive": 1,
    "Cataract_31_multiple_types|CHMP4B-related_disorder|not_specified": 1,
    "Cataract_31_multiple_types": 11,
    "CHMP4B-related_disorder": 2,
    "not_provided|Cataract_31_multiple_types": 1,
    "not_specified|ASIP-related_condition": 2,
    "ASIP-related_condition": 4,
    "not_provided|ASIP-related_condition": 1,
    "ASIP-related_condition|not_specified": 1,
    "SKIN/HAIR/EYE_PIGMENTATION_9|_DARK/LIGHT_HAIR": 1,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase": 222,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|not_provided": 9,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|Inborn_genetic_diseases": 8,
    "Hypermethioninemia": 2,
    "Inborn_genetic_diseases|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase": 11,
    "AHCY-related_disorder": 1,
    "not_provided|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase": 8,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|AHCY-related_disorder": 1,
    "Inborn_genetic_diseases|Rhabdomyolysis|not_provided|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase": 1,
    "not_provided|AHCY-related_disorder|Inborn_genetic_diseases|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase": 1,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|Inborn_genetic_diseases|not_provided": 1,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|not_provided|Inborn_genetic_diseases": 1,
    "Rhabdomyolysis|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|Inborn_genetic_diseases": 1,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|not_specified": 1,
    "not_specified|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase": 2,
    "Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|not_specified|Inborn_genetic_diseases": 1,
    "Hypermethioninemia|Hypermethioninemia_with_deficiency_of_S-adenosylhomocysteine_hydrolase|not_provided": 1,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency": 376,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|ITCH-related_disorder": 6,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|Inborn_genetic_diseases": 11,
    "not_provided|Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency": 9,
    "Inborn_genetic_diseases|Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency": 12,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|not_provided": 3,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|not_provided|ITCH-related_disorder": 1,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|ITCH-related_disorder|Inborn_genetic_diseases": 1,
    "Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "ITCH-related_disorder|Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency": 2,
    "not_specified|Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|ITCH-related_disorder|not_provided": 1,
    "ITCH-related_disorder|Syndromic_multisystem_autoimmune_disease_due_to_ITCH_deficiency|Inborn_genetic_diseases": 1,
    "ITCH-related_disorder": 3,
    "Glycosylphosphatidylinositol_biosynthesis_defect_21": 9,
    "not_provided|PIGU-related_disorder": 2,
    "PIGU-related_disorder": 5,
    "PIGU-related_disorder|not_provided": 2,
    "not_provided|Glycosylphosphatidylinositol_biosynthesis_defect_21": 2,
    "ACSS2-related_disorder": 11,
    "not_specified|ACSS2-related_disorder": 1,
    "not_provided|ACSS2-related_disorder": 2,
    "Nonsyndromic_cleft_lip_palate|not_provided": 1,
    "Inherited_glutathione_synthetase_deficiency": 28,
    "Inherited_glutathione_synthetase_deficiency|not_provided": 6,
    "not_provided|Inherited_glutathione_synthetase_deficiency": 4,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 213,
    "Glutathione_synthetase_deficiency_without_5-oxoprolinuria|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 8,
    "Inborn_genetic_diseases|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_specified": 1,
    "Inherited_glutathione_synthetase_deficiency|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Inherited_glutathione_synthetase_deficiency": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided": 3,
    "Inherited_glutathione_synthetase_deficiency|not_provided|Inborn_genetic_diseases|Glutathione_synthetase_deficiency_without_5-oxoprolinuria|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Glutathione_synthetase_deficiency_without_5-oxoprolinuria": 5,
    "Inborn_genetic_diseases|GSS-related_disorder|Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided": 1,
    "Inborn_genetic_diseases|Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Glutathione_synthetase_deficiency_without_5-oxoprolinuria|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Inherited_glutathione_synthetase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 2,
    "not_specified|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 3,
    "Inborn_genetic_diseases|not_provided|Inherited_glutathione_synthetase_deficiency": 3,
    "Inherited_glutathione_synthetase_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "GSS-related_disorder|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Inherited_glutathione_synthetase_deficiency|not_provided": 1,
    "not_provided|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 7,
    "Inherited_glutathione_synthetase_deficiency|Inborn_genetic_diseases|not_provided": 3,
    "GSS-related_disorder|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_specified|not_provided|Inherited_glutathione_synthetase_deficiency": 1,
    "Inborn_genetic_diseases|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 7,
    "not_specified|Inherited_glutathione_synthetase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided|Inherited_glutathione_synthetase_deficiency": 1,
    "Inherited_glutathione_synthetase_deficiency|not_specified": 2,
    "Inborn_genetic_diseases|Inherited_glutathione_synthetase_deficiency": 2,
    "not_specified|not_provided|Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Inborn_genetic_diseases": 1,
    "Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided|not_specified": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Glutathione_synthetase_deficiency_without_5-oxoprolinuria|Inherited_glutathione_synthetase_deficiency": 1,
    "GSS-related_disorder": 1,
    "not_provided|not_specified|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Glutathione_synthetase_deficiency_without_5-oxoprolinuria|not_provided|Inherited_glutathione_synthetase_deficiency": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Inborn_genetic_diseases": 1,
    "Glutathione_synthetase_deficiency_without_5-oxoprolinuria|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided|Inherited_glutathione_synthetase_deficiency|GSS-related_disorder": 1,
    "not_provided|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Glutathione_synthetase_deficiency_without_5-oxoprolinuria": 2,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Inborn_genetic_diseases|not_provided|Inherited_glutathione_synthetase_deficiency": 1,
    "not_provided|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Inborn_genetic_diseases|not_specified": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_specified": 2,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Glutathione_synthetase_deficiency_without_5-oxoprolinuria|not_provided": 1,
    "Glutathione_synthetase_deficiency_without_5-oxoprolinuria": 1,
    "Glutathione_synthetase_deficiency_with_5-oxoprolinuria|not_provided|not_specified|Glutathione_synthetase_deficiency_without_5-oxoprolinuria": 1,
    "Inborn_genetic_diseases|not_specified|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Inborn_genetic_diseases|Glutathione_synthetase_deficiency_without_5-oxoprolinuria|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria|Glutathione_synthetase_deficiency_without_5-oxoprolinuria|not_provided": 1,
    "not_provided|Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_with_5-oxoprolinuria": 1,
    "not_specified|Inherited_glutathione_synthetase_deficiency|Glutathione_synthetase_deficiency_without_5-oxoprolinuria": 1,
    "MYH7B-related_disorder|not_provided": 15,
    "not_provided|MYH7B-related_disorder": 23,
    "MYH7B-related_hypertrophic_cardiomyopathy": 2,
    "not_provided|not_specified|MYH7B-related_disorder": 1,
    "MYH7B-related_disorder": 9,
    "Hypertrophic_cardiomyopathy|Dilated_cardiomyopathy_with_left_ventricular_noncompaction": 2,
    "not_specified|MYH7B-related_disorder|not_provided": 2,
    "not_provided|Short_stature|not_specified": 1,
    "Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Grebe_syndrome|Brachydactyly|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 3,
    "Brachydactyly|not_provided|Grebe_syndrome|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B": 3,
    "Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Grebe_syndrome|Brachydactyly|not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 6,
    "Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Brachydactyly|Grebe_syndrome|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 2,
    "Brachydactyly|Grebe_syndrome|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B": 6,
    "not_provided|Symphalangism|_proximal|_1B": 1,
    "Brachydactyly_type_C": 5,
    "Multiple_synostoses_syndrome_2": 1,
    "GDF5-related_disorder|Type_A2_brachydactyly|Brachydactyly_type_A1C|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Multiple_synostoses_syndrome_2|Symphalangism|_proximal|_1B|Grebe_syndrome|Osteoarthritis_susceptibility_5|Brachydactyly_type_C|Acromesomelic_dysplasia_2B": 1,
    "Brachydactyly|not_provided|Grebe_syndrome|Acromesomelic_dysplasia_2B|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Multiple_synostoses_syndrome_2": 1,
    "Type_A2_brachydactyly|Symphalangism|_proximal|_1B|Acromesomelic_dysplasia_2B|not_provided": 1,
    "Inborn_genetic_diseases|Symphalangism|_proximal|_1B|not_provided|Multiple_synostoses_syndrome_2": 1,
    "Acromesomelic_dysplasia_2B": 2,
    "Grebe_syndrome": 5,
    "not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Brachydactyly_type_A1C|Type_A2_brachydactyly|Brachydactyly_type_C|Acromesomelic_dysplasia_2B|Symphalangism|_proximal|_1B|Osteoarthritis_susceptibility_5|Grebe_syndrome|Multiple_synostoses_syndrome_2": 1,
    "Brachydactyly_type_A1C|Grebe_syndrome": 1,
    "Brachydactyly_type_A1C": 1,
    "not_provided|Grebe_syndrome": 1,
    "Grebe_syndrome|Type_A2_brachydactyly|not_provided": 1,
    "Symphalangism|_proximal|_1B": 1,
    "Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Brachydactyly|not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome": 1,
    "Grebe_syndrome|not_provided": 1,
    "GDF5OS-related_condition|not_provided": 1,
    "Multiple_synostoses_syndrome_2|Grebe_syndrome|Acromesomelic_dysplasia_2B|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|not_specified|not_provided|Brachydactyly": 3,
    "GDF5-related_disorder|not_provided": 4,
    "Acromesomelic_dysplasia_2B|Multiple_synostoses_syndrome_2|Brachydactyly|GDF5-related_disorder|not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome": 1,
    "not_provided|Brachydactyly_type_C": 1,
    "not_provided|GDF5OS-related_condition": 1,
    "Acromesomelic_dysplasia_2B|Multiple_synostoses_syndrome_2|Brachydactyly|not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome": 1,
    "not_provided|Brachydactyly_type_C|Multiple_synostoses_syndrome_2": 1,
    "not_specified|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|Acromesomelic_dysplasia_2B|Multiple_synostoses_syndrome_2|Brachydactyly|not_provided": 1,
    "not_provided|Grebe_syndrome|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Osteoarthritis_susceptibility_5|Type_A2_brachydactyly|Brachydactyly_type_C|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Brachydactyly_type_A1C|Symphalangism|_proximal|_1B": 1,
    "Brachydactyly_type_A1C|Type_A2_brachydactyly|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|Osteoarthritis_susceptibility_5|Brachydactyly_type_C|Acromesomelic_dysplasia_2B|Symphalangism|_proximal|_1B|Multiple_synostoses_syndrome_2": 1,
    "not_provided|GDF5-related_disorder": 3,
    "Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|Acromesomelic_dysplasia_2B|Multiple_synostoses_syndrome_2|not_provided|not_specified|Brachydactyly": 1,
    "Inborn_genetic_diseases|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Brachydactyly_type_C|Acromesomelic_dysplasia_2B|Symphalangism|_proximal|_1B|Type_A2_brachydactyly|Brachydactyly_type_A1C|Grebe_syndrome|Multiple_synostoses_syndrome_2|not_provided": 1,
    "Brachydactyly|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|not_provided|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B": 1,
    "GDF5-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|Acromesomelic_dysplasia_2B|not_specified|Brachydactyly": 1,
    "Inborn_genetic_diseases|Grebe_syndrome": 1,
    "Osteoarthritis_susceptibility_5": 1,
    "Brachydactyly_type_C|not_provided": 1,
    "Brachydactyly|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B": 1,
    "not_provided|GDF5-related_disorder|Inborn_genetic_diseases": 1,
    "Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Grebe_syndrome|Brachydactyly|Inborn_genetic_diseases|not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 1,
    "not_provided|Brachydactyly_type_A1C|Brachydactyly_type_C|Type_A2_brachydactyly": 1,
    "Brachydactyly_type_C|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Acromesomelic_dysplasia_2B|Type_A2_brachydactyly|Grebe_syndrome|Multiple_synostoses_syndrome_2|Brachydactyly_type_A1C|Symphalangism|_proximal|_1B": 1,
    "Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Grebe_syndrome|Acromesomelic_dysplasia_2B|Multiple_synostoses_syndrome_2|Brachydactyly|not_provided": 1,
    "Acromesomelic_dysplasia_2B|Acromesomelic_dysplasia|Chondrodysplasia|Symphalangism-brachydactyly_syndrome|Brachydactyly": 1,
    "Multiple_synostoses_syndrome_2|Grebe_syndrome|Acromesomelic_dysplasia_2B|Brachydactyly|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 1,
    "Brachydactyly|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Multiple_synostoses_syndrome_2|Acromesomelic_dysplasia_2B|Grebe_syndrome": 1,
    "Multiple_synostoses_syndrome_2|Grebe_syndrome|Acromesomelic_dysplasia_2B|Brachydactyly|not_provided|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type": 1,
    "Brachydactyly|Grebe_syndrome|Acromesomelic_dysplasia_2B|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Multiple_synostoses_syndrome_2": 1,
    "not_provided|Acromesomelic_dysplasia_2B|Multiple_synostoses_syndrome_2|Grebe_syndrome|Acromesomelic_dysplasia_2C|_Hunter-Thompson_type|Osteoarthritis_susceptibility_5|Brachydactyly": 1,
    "Cone-rod_dystrophy_and_hearing_loss_2": 14,
    "not_provided|CEP250-related_disorder": 16,
    "CEP250-related_disorder|not_provided": 15,
    "not_provided|Cone-rod_dystrophy_and_hearing_loss_2": 9,
    "CEP250-related_disorder": 10,
    "Retinal_dystrophy|Cone-rod_dystrophy_and_hearing_loss_2|not_provided|CEP250-related_disorder": 1,
    "Cone-rod_dystrophy_and_hearing_loss_2|not_provided": 8,
    "CEP250-related_disorder|Cone-rod_dystrophy_and_hearing_loss_2|not_provided": 1,
    "Cone-rod_dystrophy_and_hearing_loss_2|Usher_syndrome|not_provided": 1,
    "Schizophrenia_19": 4,
    "RBM12-related_disorder": 5,
    "RBM12-related_disorder|Schizophrenia_19": 1,
    "not_provided|RBM12-related_disorder": 1,
    "not_provided|NFS1-related_disorder": 1,
    "not_provided|not_specified|NFS1-related_disorder": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency_52": 3,
    "NFS1-related_disorder|not_provided": 1,
    "NFS1-related_disorder": 3,
    "Intellectual_disability|_autosomal_dominant_11": 10,
    "not_provided|Intellectual_disability|_autosomal_dominant_11": 1,
    "not_specified|EPB41L1-related_disorder": 1,
    "Intellectual_disability|_autosomal_dominant_11|not_specified": 2,
    "EPB41L1-related_disorder": 7,
    "EPB41L1-related_disorder|not_specified|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_11|not_specified|Complex_neurodevelopmental_disorder": 1,
    "not_provided|EPB41L1-related_disorder|not_specified": 1,
    "Anteriorly_placed_anus|Cerebellar_malformation|Macule|Patent_foramen_ovale|Hypoplasia_of_the_corpus_callosum|Microcephaly|Ventricular_septal_defect|Global_developmental_delay": 1,
    "Visceral_myopathy_1|not_specified|Megacystis-microcolon-intestinal_hypoperistalsis_syndrome_4": 1,
    "Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_syndrome_2|Bilateral_cleft_lip_and_palate|Macrocephaly|Intellectual_disability|Hypertelorism|Flat_face|Bifid_ribs|Rib_fusion|Abnormality_of_the_vertebral_column|Micrognathia|Scoliosis|Craniofacial_dysmorphism|_skeletal_anomalies|_and_impaired_intellectual_development_1": 1,
    "Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2": 40,
    "Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2|not_provided": 7,
    "Aicardi-Goutieres_syndrome_5|not_specified|Chilblain_lupus_2|not_provided": 1,
    "Aicardi-Goutieres_syndrome_5": 661,
    "Aicardi-Goutieres_syndrome_5|not_specified": 4,
    "Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome": 24,
    "not_provided|Aicardi-Goutieres_syndrome_5|Inborn_genetic_diseases|Aicardi_Goutieres_syndrome": 1,
    "Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5": 3,
    "SAMHD1-related_disorder|Aicardi-Goutieres_syndrome_5": 2,
    "not_provided|Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome": 1,
    "SAMHD1-related_disorder": 6,
    "not_provided|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5": 1,
    "not_provided|Aicardi_Goutieres_syndrome|not_specified|SAMHD1-related_disorder|Aicardi-Goutieres_syndrome_5": 1,
    "Aicardi-Goutieres_syndrome_5|SAMHD1-related_disorder|not_specified|Chilblain_lupus_2": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_5": 11,
    "Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_5": 1,
    "Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5|not_provided": 1,
    "not_provided|Aicardi-Goutieres_syndrome_5": 8,
    "not_specified|Chilblain_lupus_2|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5|Inborn_genetic_diseases|not_provided": 1,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5": 13,
    "not_provided|Aicardi-Goutieres_syndrome_5|Inborn_genetic_diseases": 1,
    "Aicardi_Goutieres_syndrome|not_provided": 1,
    "Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome": 1,
    "Chilblain_lupus_2|Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome": 1,
    "Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2|Aicardi_Goutieres_syndrome": 1,
    "SAMHD1-related_disorder|Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5|not_provided": 1,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2": 1,
    "Aicardi-Goutieres_syndrome_5|Inborn_genetic_diseases": 4,
    "Aicardi-Goutieres_syndrome_5|not_provided": 8,
    "Aicardi-Goutieres_syndrome_5|SAMHD1-related_disorder": 2,
    "Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2": 1,
    "Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome|Chilblain_lupus_2": 2,
    "Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_5|SAMHD1-related_disorder": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome": 2,
    "Aicardi-Goutieres_syndrome_5|Inborn_genetic_diseases|Aicardi_Goutieres_syndrome": 1,
    "Aicardi-Goutieres_syndrome_5|not_provided|Aicardi_Goutieres_syndrome": 1,
    "not_provided|Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5": 1,
    "not_specified|Aicardi-Goutieres_syndrome_5": 3,
    "Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5|not_provided": 2,
    "Aicardi-Goutieres_syndrome_5|not_specified|Aicardi_Goutieres_syndrome": 1,
    "Inborn_genetic_diseases|Aicardi_Goutieres_syndrome": 1,
    "SAMHD1-related_disorder|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5": 1,
    "Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2|not_specified": 1,
    "Aicardi_Goutieres_syndrome|Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5|not_provided": 2,
    "not_provided|Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome": 1,
    "Inborn_genetic_diseases|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5": 2,
    "not_specified|not_provided|Aicardi_Goutieres_syndrome": 1,
    "Aicardi_Goutieres_syndrome|Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5": 1,
    "not_specified|not_provided|Aicardi-Goutieres_syndrome_5": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_5|Chilblain_lupus_2": 1,
    "Aicardi-Goutieres_syndrome_5|not_provided|Chilblain_lupus_2|SAMHD1-related_disorder": 1,
    "not_specified|Aicardi-Goutieres_syndrome_5|not_provided|Chilblain_lupus_2": 1,
    "not_specified|Aicardi_Goutieres_syndrome|Aicardi-Goutieres_syndrome_5": 1,
    "Inborn_genetic_diseases|not_provided|Aicardi-Goutieres_syndrome_5": 1,
    "not_specified|Aicardi_Goutieres_syndrome|not_provided|Aicardi-Goutieres_syndrome_5": 1,
    "Aicardi-Goutieres_syndrome_5|not_provided|Chilblain_lupus_2": 1,
    "Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome|not_specified|SAMHD1-related_disorder": 1,
    "Inborn_genetic_diseases|Aicardi-Goutieres_syndrome_5|not_specified": 1,
    "Aicardi-Goutieres_syndrome_5|Aicardi_Goutieres_syndrome|SAMHD1-related_disorder": 1,
    "Cerebral_palsy|not_provided": 1,
    "Aicardi-Goutieres_syndrome_5|not_provided|Aicardi_Goutieres_syndrome|Chilblain_lupus_2": 1,
    "Chilblain_lupus_2|Aicardi-Goutieres_syndrome_5|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Chilblain_lupus_2|not_provided|Aicardi-Goutieres_syndrome_5": 1,
    "not_provided|not_specified|Congenital_disorder_of_glycosylation": 1,
    "not_provided|SRC-related_disorder|not_specified": 1,
    "SRC-related_disorder": 7,
    "not_provided|SRC-related_disorder": 2,
    "SRC-related_disorder|not_provided|not_specified": 1,
    "Thrombocytopenia_6": 3,
    "Osteoporosis|Primary_myelofibrosis|Thrombocytopenia|Thrombocytopenia_6": 1,
    "Colon_cancer|_advanced": 1,
    "Immunodeficiency_99_with_hypogammaglobulinemia_and_autoimmune_cytopenias": 1,
    "Intellectual_disability|_severe": 2,
    "Neurodevelopmental_disorder_with_microcephaly_and_movement_abnormalities": 7,
    "Neurodevelopmental_disorder_with_microcephaly_and_movement_abnormalities|Abnormal_brain_morphology": 1,
    "RALGAPB-related_disorder": 14,
    "RALGAPB-related_disorder|not_specified": 1,
    "SLC32A1-related_epilepsy": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_12|Developmental_and_epileptic_encephalopathy_114|Intellectual_disability|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy_114": 1,
    "Intellectual_disability|Seizure|Developmental_and_epileptic_encephalopathy_114": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_12|Generalized_epilepsy_with_febrile_seizures_plus": 2,
    "Mild_global_developmental_delay|Obesity|Generalized-onset_seizure": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_12|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_12|Generalized_epilepsy_with_febrile_seizures_plus|not_provided": 1,
    "Generalized_epilepsy_with_febrile_seizures_plus|_type_12|not_provided|Generalized_epilepsy_with_febrile_seizures_plus": 1,
    "not_provided|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 11,
    "Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 70,
    "MAFB-related_disorder": 9,
    "Duane_retraction_syndrome_3_with_or_without_deafness|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 15,
    "not_provided|MAFB-related_disorder": 2,
    "MAFB-related_disorder|not_provided": 5,
    "Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness|not_provided": 2,
    "Inborn_genetic_diseases|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness|not_provided": 1,
    "Duane_retraction_syndrome_3_with_or_without_deafness|Duane_retraction_syndrome_2|Duane_syndrome_type_1": 3,
    "not_provided|Duane_retraction_syndrome_3_with_or_without_deafness|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 2,
    "Duane_retraction_syndrome_3_with_or_without_deafness|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|MAFB-related_disorder|not_specified|not_provided": 1,
    "Duane_retraction_syndrome_3_with_or_without_deafness|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|not_provided": 3,
    "not_provided|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness": 2,
    "MAFB-related_disorder|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 2,
    "Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness|Inborn_genetic_diseases|not_provided": 1,
    "Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness|not_provided|MAFB-related_disorder|Inborn_genetic_diseases": 1,
    "Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Duane_retraction_syndrome_3_with_or_without_deafness|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Duane_retraction_syndrome_3_with_or_without_deafness|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|not_provided": 1,
    "not_provided|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy|Inborn_genetic_diseases": 1,
    "MAFB-related_disorder|not_provided|not_specified|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 1,
    "Carpal_osteolysis|Multicentric_carpo-tarsal_osteolysis_with_or_without_nephropathy": 1,
    "TOP1-related_disorder": 4,
    "not_provided|TOP1-related_disorder": 1,
    "DNA_topoisomerase_I|_camptothecin-resistant": 1,
    "TOP1-related_disorder|not_provided": 1,
    "PLCG1-related_disorder": 8,
    "Immune_dysregulation|_autoimmunity|_and_autoinflammation|not_specified": 1,
    "ZHX3-related_disorder|not_provided": 5,
    "ZHX3-related_disorder": 1,
    "not_provided|ZHX3-related_disorder": 1,
    "PTPRT-related_disorder": 22,
    "not_specified|Abnormality_of_neuronal_migration": 1,
    "not_provided|PTPRT-related_disorder": 21,
    "PTPRT-associated_neurodevelopmentaldisorder": 1,
    "PTPRT-related_disorder|not_provided": 7,
    "PTPRT-associated_neurodevelopmental_disorder": 1,
    "L3MBTL1-related_disorder": 5,
    "not_provided|IFT52-related_disorder": 2,
    "Short-rib_thoracic_dysplasia_16_with_or_without_polydactyly|not_provided": 2,
    "Short-rib_thoracic_dysplasia_16_with_or_without_polydactyly": 4,
    "IFT52-related_disorder|not_provided": 3,
    "Short_rib-polydactyly_syndrome|Short-rib_thoracic_dysplasia_16_with_or_without_polydactyly|not_provided": 1,
    "Short-rib_thoracic_dysplasia_16_with_or_without_polydactyly|Short_rib-polydactyly_syndrome": 1,
    "IFT52-related_disorder": 1,
    "not_specified|Short-rib_thoracic_dysplasia_16_with_or_without_polydactyly": 1,
    "MYBL2-related_condition": 1,
    "not_provided|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 1,
    "Cardiomyopathy|_dilated|_2E": 6,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 5,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 5,
    "Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|JPH2-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|not_specified": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 5,
    "Cardiovascular_phenotype|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 4,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|not_provided|Hypertrophic_cardiomyopathy": 3,
    "Cardiovascular_phenotype|JPH2-related_disorder": 2,
    "Cardiovascular_phenotype|JPH2-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy": 1,
    "JPH2-related_disorder": 5,
    "JPH2-related_disorder|Cardiovascular_phenotype": 5,
    "Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E": 2,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_17": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|JPH2-related_disorder": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E": 1,
    "Hypertrophic_cardiomyopathy|JPH2-related_disorder|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 5,
    "Hypertrophic_cardiomyopathy|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|not_provided": 2,
    "JPH2-related_disorder|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy": 2,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy_17": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17": 1,
    "Hypertrophic_cardiomyopathy_17|not_provided|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy": 1,
    "JPH2-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|JPH2-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|not_provided|not_specified|Hypertrophic_cardiomyopathy": 2,
    "not_provided|JPH2-related_disorder|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17|not_specified|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 3,
    "Cardiomyopathy|_dilated|_2E|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17": 1,
    "Hypertrophic_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17": 1,
    "JPH2-related_disorder|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy": 1,
    "Long_QT_syndrome|Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E|not_specified|Hypertrophic_cardiomyopathy_17|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|not_provided|not_specified|Hypertrophic_cardiomyopathy_17|JPH2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|JPH2-related_disorder": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy_17": 5,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17": 1,
    "Cardiovascular_phenotype|Supraventricular_tachycardia|Cardiomyopathy|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17": 1,
    "JPH2-related_disorder|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|JPH2-related_disorder|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy_17|not_provided|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified": 1,
    "not_specified|not_provided|Hypertrophic_cardiomyopathy|JPH2-related_disorder|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Ventricular_fibrillation|_paroxysmal_familial|_type_1|Hypertrophic_cardiomyopathy": 1,
    "JPH2-related_disorder|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy": 1,
    "JPH2-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|Hypertrophic_cardiomyopathy_17|not_provided": 1,
    "Cardiovascular_phenotype|JPH2-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype|not_provided": 1,
    "Hypertrophic_cardiomyopathy|not_provided|JPH2-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Hypertrophic_cardiomyopathy_17": 1,
    "not_specified|Cardiovascular_phenotype|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|JPH2-related_disorder|Hypertrophic_cardiomyopathy": 1,
    "Hypertrophic_cardiomyopathy_17|Hypertrophic_cardiomyopathy_1|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy_17|Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|_dilated|_2E|Hypertrophic_cardiomyopathy_17|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Hypertrophic_cardiomyopathy|Cardiomyopathy|_dilated|_2E|not_provided|not_specified|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|JPH2-related_disorder|not_specified|not_provided|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype": 1,
    "Hypertrophic_cardiomyopathy|Hypertrophic_cardiomyopathy_17|Cardiovascular_phenotype": 1,
    "not_provided|FITM2-related_disorder": 1,
    "FITM2-related_disorder": 3,
    "not_provided|Siddiqi_syndrome": 1,
    "Siddiqi_syndrome": 7,
    "FITM2-related_disorder|not_provided": 4,
    "Siddiqi_syndrome|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|HNF4A-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_1": 26,
    "HNF4A-related_disorder|Monogenic_diabetes": 2,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1": 7,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus": 22,
    "Hyperinsulinism_due_to_HNF1A_deficiency": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Hyperinsulinism|_Dominant": 1,
    "not_provided|not_specified|HNF4A-related_disorder": 1,
    "HNF4A-related_disorder": 14,
    "Maturity_onset_diabetes_mellitus_in_young|HNF4A-related_disorder|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|not_provided": 1,
    "not_provided|HNF4A-related_disorder": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 1,
    "HNF4A-related_disorder|not_provided": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1": 9,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Glycosuria|Maturity_onset_diabetes_mellitus_in_young|not_specified|Hyperinsulinism|_Dominant|not_provided": 1,
    "not_specified|HNF4A-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity_onset_diabetes_mellitus_in_young|not_provided": 3,
    "not_provided|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Monogenic_diabetes": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|not_provided|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|HNF4A-related_disorder|Maturity-onset_diabetes_of_the_young_type_1|not_provided|Familial_hyperinsulinism|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Monogenic_diabetes|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinemia": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1": 2,
    "Monogenic_diabetes|Hyperinsulinism_due_to_HNF4A_deficiency|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|not_provided|Monogenic_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified|Monogenic_diabetes|Hyperinsulinism|_Dominant": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|HNF4A-related_disorder": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes": 3,
    "Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes|not_provided": 3,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|not_provided|Monogenic_diabetes": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF4A-related_disorder|not_provided|Monogenic_diabetes": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|not_provided": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|not_specified|not_provided": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 2,
    "not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|HNF4A-related_disorder|Monogenic_diabetes": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "not_provided|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes|Familial_hyperinsulinism|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|not_specified|Type_2_diabetes_mellitus": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Familial_hyperinsulinism|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|not_provided": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Monogenic_diabetes": 1,
    "HNF4A-related_disorder|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1": 2,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Monogenic_diabetes|not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1": 2,
    "Monogenic_diabetes|not_specified|not_provided|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1": 3,
    "Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|HNF4A-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young|not_provided|not_specified|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|not_provided|Familial_hyperinsulinism": 2,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Monogenic_diabetes": 1,
    "not_provided|not_specified|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Monogenic_diabetes|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|not_provided|Familial_hyperinsulinism|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|not_provided": 2,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided|Familial_hyperinsulinism": 3,
    "Monogenic_diabetes|HNF4A-related_disorder|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young|HNF4A-related_disorder|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 19,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|not_provided|Monogenic_diabetes": 1,
    "Hyperinsulinism|_Dominant|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "HNF4A-related_disorder|not_specified": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes": 1,
    "Monogenic_diabetes|not_provided|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|not_specified": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided|Familial_hyperinsulinism": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|HNF4A-related_disorder|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|HNF4A-related_disorder": 1,
    "not_specified|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|not_provided": 1,
    "not_specified|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity_onset_diabetes_mellitus_in_young|not_provided|HNF4A-related_disorder": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_1|HNF4A-related_disorder|Hyperinsulinemia": 1,
    "not_specified|not_provided|Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes|not_provided|HNF4A-related_disorder": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young|HNF4A-related_disorder|not_provided|Monogenic_diabetes|not_specified": 1,
    "Monogenic_diabetes|Hyperinsulinism_due_to_HNF4A_deficiency|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided|Maturity_onset_diabetes_mellitus_in_young|Monogenic_diabetes": 1,
    "not_provided|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus": 2,
    "Monogenic_diabetes|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus": 1,
    "not_specified|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided|HNF4A-related_disorder|Maturity_onset_diabetes_mellitus_in_young": 1,
    "not_provided|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "HNF4A-related_disorder|not_specified|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus": 1,
    "not_specified|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Monogenic_diabetes|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|not_provided": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified": 1,
    "HNF4A-related_disorder|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|HNF4A-related_disorder|not_provided": 1,
    "Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Monogenic_diabetes|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|not_provided": 1,
    "Monogenic_diabetes|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|not_provided|not_specified": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Monogenic_diabetes|Familial_hyperinsulinism": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|not_provided|not_specified|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Monogenic_diabetes|Type_2_diabetes_mellitus|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity_onset_diabetes_mellitus_in_young|not_specified|not_provided": 1,
    "Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1": 3,
    "not_specified|Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Autosomal_dominant_polycystic_liver_disease|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Maturity-onset_diabetes_of_the_young_type_1|Type_2_diabetes_mellitus|Monogenic_diabetes|not_specified|Maturity_onset_diabetes_mellitus_in_young|not_provided|Familial_hyperinsulinism": 1,
    "Familial_hyperinsulinism|not_provided|Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1|not_specified": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Fanconi_renotubular_syndrome_4_with_maturity-onset_diabetes_of_the_young|Type_2_diabetes_mellitus|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|not_provided": 2,
    "not_specified|not_provided|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism": 20,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 1,
    "Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1": 7,
    "Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1|not_provided": 1,
    "not_provided|Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Familial_hyperinsulinism|not_provided|Maturity-onset_diabetes_of_the_young_type_1": 5,
    "Maturity_onset_diabetes_mellitus_in_young|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|not_provided": 2,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 1,
    "Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism|_Dominant": 15,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism": 2,
    "Familial_hyperinsulinism|not_provided|Maturity-onset_diabetes_of_the_young_type_1": 1,
    "Maturity_onset_diabetes_mellitus_in_young|not_provided|Hyperinsulinism|_Dominant": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|not_provided|Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 6,
    "not_provided|Maturity_onset_diabetes_mellitus_in_young|Hyperinsulinism|_Dominant": 1,
    "not_provided|Maturity-onset_diabetes_of_the_young_type_1|Familial_hyperinsulinism|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Familial_hyperinsulinism|Maturity-onset_diabetes_of_the_young_type_1|Maturity_onset_diabetes_mellitus_in_young": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 571,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 23,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_provided": 14,
    "SCID_due_to_ADA_deficiency|_delayed_onset|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Inborn_genetic_diseases|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "ADA-related_disorder": 2,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency_disease": 2,
    "not_provided|ADA-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|SCID_due_to_ADA_deficiency|_delayed_onset": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified": 7,
    "Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 7,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified": 4,
    "not_specified|ADA-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|ADA-related_disorder": 1,
    "Severe_combined_immunodeficiency_disease|ADA-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|Partial_adenosine_deaminase_deficiency|not_provided": 1,
    "not_provided|Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 2,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|ADA-related_disorder|not_provided": 1,
    "not_provided|ADA-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Partial_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 2,
    "ADA-related_disorder|not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency_disease": 2,
    "not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 4,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|ADA-related_disorder": 3,
    "ADA-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 3,
    "ADA-related_disorder|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Partial_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|Partial_adenosine_deaminase_deficiency": 1,
    "not_specified|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|ADA-related_disorder|not_specified": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|ADA-related_disorder|Severe_combined_immunodeficiency_disease": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified|not_provided": 1,
    "Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_provided": 2,
    "Severe_combined_immunodeficiency_disease|SCID_due_to_ADA_deficiency|_delayed_onset|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "not_provided|Severe_combined_immunodeficiency_disease|Partial_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Partial_adenosine_deaminase_deficiency|not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_provided|ADA-related_disorder": 1,
    "ADA-related_disorder|Severe_combined_immunodeficiency_disease|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "ADA-related_disorder|not_specified|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|not_specified|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "Severe_combined_immunodeficiency_disease|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "not_provided|not_specified|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "not_provided|Partial_adenosine_deaminase_deficiency|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency": 1,
    "ADA-related_disorder|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified|not_provided|ADA-related_disorder": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_provided|not_specified": 1,
    "Adenosine_deaminase_2_allozyme|not_provided|Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-negative|_due_to_adenosine_deaminase_deficiency|not_specified": 1,
    "Oocyte/zygote/embryo_maturation_arrest_22": 8,
    "Combined_immunodeficiency_due_to_STK4_deficiency": 191,
    "not_specified|Combined_immunodeficiency_due_to_STK4_deficiency|not_provided": 2,
    "not_provided|Combined_immunodeficiency_due_to_STK4_deficiency": 4,
    "STK4-related_disorder|Combined_immunodeficiency_due_to_STK4_deficiency": 1,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_STK4_deficiency": 13,
    "Inherited_Immunodeficiency_Diseases|Combined_immunodeficiency_due_to_STK4_deficiency|STK4-related_disorder": 1,
    "Combined_immunodeficiency_due_to_STK4_deficiency|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Combined_immunodeficiency_due_to_STK4_deficiency|STK4-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Combined_immunodeficiency_due_to_STK4_deficiency": 1,
    "STK4-related_disorder": 2,
    "not_provided|Combined_immunodeficiency_due_to_STK4_deficiency|Inborn_genetic_diseases": 1,
    "Combined_immunodeficiency_due_to_STK4_deficiency|not_provided": 3,
    "not_provided|not_specified|Combined_immunodeficiency_due_to_STK4_deficiency": 1,
    "Combined_immunodeficiency_due_to_STK4_deficiency|STK4-related_disorder": 1,
    "MATN4-related_disorder": 11,
    "MATN4-related_disorder|not_provided": 2,
    "not_provided|MATN4-related_disorder": 1,
    "Global_developmental_delay|Proptosis|Seizure|Diabetes_insipidus|Holoprosencephaly_sequence|Lumbosacral_myelomeningocele|Microcephaly": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 140,
    "not_provided|PIGT-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 3,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided": 2,
    "PIGT-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Paroxysmal_nocturnal_hemoglobinuria_2": 2,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 8,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 20,
    "Paroxysmal_nocturnal_hemoglobinuria_2": 4,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided": 17,
    "not_provided|PIGT-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Inborn_genetic_diseases": 9,
    "PIGT-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 3,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Paroxysmal_nocturnal_hemoglobinuria_2": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Paroxysmal_nocturnal_hemoglobinuria_1": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 1,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|PIGT-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Paroxysmal_nocturnal_hemoglobinuria_2": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided|Paroxysmal_nocturnal_hemoglobinuria_2": 1,
    "PIGT-related_disorder": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided|PIGT-related_disorder": 1,
    "not_specified|not_provided|PIGT-related_disorder|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3": 1,
    "Neurodevelopmental_delay|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|not_provided|Global_developmental_delay|Seizure": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Paroxysmal_nocturnal_hemoglobinuria_2|not_provided": 2,
    "not_specified|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|Paroxysmal_nocturnal_hemoglobinuria_2": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_3|High_myopia": 1,
    "Bronchiectasis_and_nasal_polyposis": 2,
    "Bronchiectasis_and_nasal_polyposis|not_specified": 1,
    "Congenital_myopathy_15": 2,
    "not_provided|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 13,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase": 440,
    "Inborn_genetic_diseases|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 6,
    "CTSA-related_disorder|Inborn_genetic_diseases|not_provided|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 1,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|Inborn_genetic_diseases": 9,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|not_specified": 3,
    "CTSA-related_disorder|not_provided|Combined_deficiency_of_sialidase_AND_beta_galactosidase|not_specified": 1,
    "not_specified|Combined_deficiency_of_sialidase_AND_beta_galactosidase|not_provided": 1,
    "CTSA-related_disorder|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 4,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|CTSA-related_disorder": 3,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|not_provided": 16,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|not_specified|not_provided": 3,
    "Galactosialidosis|_early_infantile|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 2,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|Galactosialidosis|_late_infantile": 1,
    "Non-immune_hydrops_fetalis|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 1,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|Galactosialidosis|_adult": 1,
    "not_specified|Combined_deficiency_of_sialidase_AND_beta_galactosidase|CTSA-related_disorder": 1,
    "CTSA-related_disorder": 2,
    "Galactosialidosis|_early_infantile": 1,
    "Galactosialidosis|_late_infantile|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 1,
    "Galactosialidosis|_late_infantile": 3,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|Cathepsin_a-related_arteriopathy-strokes-leukoencephalopathy": 1,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|Abnormality_of_prenatal_development_or_birth": 1,
    "not_specified|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 3,
    "Inborn_genetic_diseases|not_specified|Combined_deficiency_of_sialidase_AND_beta_galactosidase": 1,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|not_provided|CTSA-related_disorder": 1,
    "Combined_deficiency_of_sialidase_AND_beta_galactosidase|Galactosialidosis|_late_infantile|not_provided": 1,
    "not_provided|PLTP-related_disorder": 2,
    "PLTP-related_disorder": 3,
    "PLTP-related_disorder|not_provided": 1,
    "RECLASSIFIED_-_PLTP_POLYMORPHISM": 1,
    "not_provided|ZNF335-related_disorder": 8,
    "Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_provided": 9,
    "Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 23,
    "not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 6,
    "ZNF335-related_disorder|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|not_provided|ZNF335-related_disorder": 1,
    "ZNF335-related_disorder": 10,
    "Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_provided|not_specified": 2,
    "ZNF335-related_disorder|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_provided": 1,
    "not_specified|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_provided": 7,
    "Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_specified|not_provided": 5,
    "not_specified|not_provided|ZNF335-related_disorder": 1,
    "ZNF335-related_disorder|not_provided": 3,
    "Autism|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|Aminoacylase_1_deficiency": 1,
    "Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 3,
    "Inborn_genetic_diseases|ZNF335-related_disorder|not_provided": 1,
    "not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_specified": 1,
    "ZNF335-related_disorder|not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 1,
    "ZNF335-related_disorder|not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|not_specified": 1,
    "ZNF335-related_disorder|not_specified|not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 1,
    "not_provided|not_specified|ZNF335-related_disorder": 1,
    "not_specified|not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 3,
    "not_specified|ZNF335-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 1,
    "not_provided|ZNF335-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 1,
    "ZNF335-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|ZNF335-related_disorder|Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency": 1,
    "Microcephalic_primordial_dwarfism_due_to_ZNF335_deficiency|ZNF335-related_disorder|not_provided": 1,
    "not_provided|Metaphyseal_anadysplasia_2": 16,
    "Metaphyseal_anadysplasia_2|not_provided": 19,
    "Metaphyseal_anadysplasia_2": 17,
    "not_provided|Metaphyseal_anadysplasia_2|MMP9-related_disorder": 1,
    "MMP9-related_disorder": 1,
    "MMP9-related_disorder|not_provided": 2,
    "not_provided|MMP9-related_disorder|Metaphyseal_anadysplasia_2": 1,
    "not_specified|Metaphyseal_anadysplasia_2|not_provided": 2,
    "MMP9-related_disorder|not_provided|Metaphyseal_anadysplasia_2": 1,
    "Mendelian_syndromes_with_cleft_lip/palate|not_provided": 1,
    "not_specified|Metaphyseal_anadysplasia_2": 1,
    "not_specified|not_provided|Metaphyseal_anadysplasia_2": 1,
    "not_provided|not_specified|Metaphyseal_anadysplasia_2": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14": 1,
    "SLC12A5-related_disorder": 5,
    "Developmental_and_epileptic_encephalopathy|_34": 750,
    "not_specified|Developmental_and_epileptic_encephalopathy|_34": 15,
    "not_provided|Developmental_and_epileptic_encephalopathy|_34": 18,
    "Developmental_and_epileptic_encephalopathy|_34|not_provided": 20,
    "Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14": 4,
    "Developmental_and_epileptic_encephalopathy|_34|not_specified": 24,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_34": 1,
    "Developmental_and_epileptic_encephalopathy|_34|not_specified|not_provided": 2,
    "not_specified|See_cases|Developmental_and_epileptic_encephalopathy|_34": 1,
    "Developmental_and_epileptic_encephalopathy|_34|not_provided|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_34|Movement_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_34|SLC12A5-related_disorder|not_provided": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_14": 5,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|not_provided|Developmental_and_epileptic_encephalopathy|_34": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_34": 4,
    "Developmental_and_epileptic_encephalopathy|_34|See_cases": 1,
    "Developmental_and_epileptic_encephalopathy|_34|not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14": 2,
    "Microcephaly|Developmental_and_epileptic_encephalopathy|_34": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_34|not_specified": 1,
    "not_provided|SLC12A5-related_disorder|Developmental_and_epileptic_encephalopathy|_34": 2,
    "SLC12A5-related_disorder|Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|not_provided": 1,
    "SLC12A5-related_disorder|Developmental_and_epileptic_encephalopathy|_34": 3,
    "Developmental_and_epileptic_encephalopathy|_34|SLC12A5-related_disorder": 1,
    "SLC12A5-related_disorder|Developmental_and_epileptic_encephalopathy|_34|not_provided": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|Developmental_and_epileptic_encephalopathy|_34": 2,
    "Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|not_provided": 2,
    "Intellectual_disability|not_provided|Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|not_specified": 1,
    "not_specified|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14": 1,
    "SLC12A5-related_disorder|not_provided|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|Developmental_and_epileptic_encephalopathy|_34": 1,
    "Developmental_and_epileptic_encephalopathy|not_specified|Developmental_and_epileptic_encephalopathy|_34": 1,
    "SLC12A5-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_34": 1,
    "SLC12A5-related_disorder|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_34|Epilepsy|_idiopathic_generalized|_susceptibility_to|_14|SLC12A5-related_disorder|not_specified": 1,
    "not_provided|Hyperimmunoglobulin_M_syndrome": 2,
    "Hyper-IgM_syndrome_type_3": 17,
    "not_provided|Hyper-IgM_syndrome_type_3": 15,
    "not_specified|Hyper-IgM_syndrome_type_3|not_provided": 1,
    "CD40-related_disorder|not_provided": 1,
    "not_specified|Hyper-IgM_syndrome_type_3|Hyper-IgM_syndrome_type_1": 1,
    "not_specified|not_provided|Hyper-IgM_syndrome_type_3": 3,
    "not_provided|Hyper-IgM_syndrome_type_3|not_specified": 1,
    "Hyper-IgM_syndrome_type_3|not_provided": 4,
    "not_provided|CD40-related_disorder": 1,
    "Primary_intraosseous_venous_malformation": 9,
    "Primary_intraosseous_venous_malformation|not_provided": 2,
    "Inborn_genetic_diseases|Primary_intraosseous_venous_malformation": 1,
    "ELMO2-related_disorder": 3,
    "not_provided|Primary_intraosseous_venous_malformation": 1,
    "ELMO2-related_disorder|Primary_intraosseous_venous_malformation|not_provided": 1,
    "ELMO2-related_disorder|not_provided": 1,
    "Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate|not_provided|not_specified": 1,
    "Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate": 4,
    "Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate|Prostate_cancer|not_provided": 1,
    "not_provided|SLC13A3-related_disorder": 1,
    "SLC13A3-related_disorder|not_provided": 4,
    "not_provided|Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate|SLC13A3-related_disorder": 2,
    "Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate|not_specified": 1,
    "not_provided|Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate": 1,
    "Leukoencephalopathy|_acute_reversible|_with_increased_urinary_alpha-ketoglutarate|not_specified|not_provided": 1,
    "Galloway-Mowat_syndrome_4": 44,
    "Galloway-Mowat_syndrome_4|not_provided": 6,
    "not_provided|Global_developmental_delay|Seizure|Galloway-Mowat_syndrome_4": 1,
    "TP53RK-related_disorder": 2,
    "Galloway-Mowat_syndrome_4|not_provided|TP53RK-related_disorder": 1,
    "not_provided|Galloway-Mowat_syndrome_4|TP53RK-related_disorder": 1,
    "TP53RK-related_disorder|Galloway-Mowat_syndrome_4": 1,
    "not_specified|not_provided|Galloway-Mowat_syndrome_4": 1,
    "Galloway-Mowat_syndrome_4|TP53RK-related_disorder": 1,
    "not_provided|TP53RK-related_disorder": 3,
    "TP53RK-related_disorder|Galloway-Mowat_syndrome_4|not_provided": 1,
    "Galloway-Mowat_syndrome_4|Global_developmental_delay|Seizure": 1,
    "Galloway-Mowat_syndrome_4|Microcephaly": 1,
    "Arterial_tortuosity_syndrome": 252,
    "not_provided|Arterial_tortuosity_syndrome|not_specified": 2,
    "not_provided|Arterial_tortuosity_syndrome": 24,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 13,
    "SLC2A10-related_disorder|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 26,
    "not_specified|Arterial_tortuosity_syndrome": 6,
    "Arterial_tortuosity_syndrome|not_provided": 8,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 6,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 9,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 31,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome|SLC2A10-related_disorder": 1,
    "Ehlers-Danlos_syndrome|_classic_type|Arterial_tortuosity_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Arterial_tortuosity_syndrome": 4,
    "Arterial_tortuosity_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 20,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Arterial_tortuosity_syndrome": 4,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SLC2A10-related_disorder": 1,
    "SLC2A10-related_disorder|not_provided|Arterial_tortuosity_syndrome": 1,
    "Arterial_tortuosity_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_aortopathy|not_provided": 1,
    "SLC2A10-related_disorder": 3,
    "not_provided|Arterial_tortuosity_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_aortopathy|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 3,
    "SLC2A10-related_disorder|not_specified|Arterial_tortuosity_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome|not_provided": 3,
    "not_provided|Arterial_tortuosity_syndrome|Familial_aortopathy": 1,
    "Arterial_tortuosity_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 10,
    "Arterial_tortuosity_syndrome|SLC2A10-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Disproportionate_tall_stature|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_specified|Arterial_tortuosity_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Arterial_tortuosity_syndrome|not_specified|SLC2A10-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Arterial_tortuosity_syndrome|Cardiovascular_phenotype": 2,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome|not_provided": 2,
    "SLC2A10-related_disorder|Arterial_tortuosity_syndrome": 1,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|SLC2A10-related_disorder|not_specified": 1,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "not_specified|not_provided|Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Thoracic_aortic_aneurysm_or_dissection|Cardiovascular_phenotype|Familial_aortopathy|Arterial_tortuosity_syndrome": 1,
    "Cardiovascular_phenotype|Arterial_tortuosity_syndrome": 1,
    "not_specified|Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Arterial_tortuosity_syndrome|not_specified": 5,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|SLC2A10-related_disorder": 1,
    "SLC2A10-related_disorder|Arterial_tortuosity_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_aortopathy|Arterial_tortuosity_syndrome": 1,
    "Aortic_aneurysm|_familial_thoracic_6|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 1,
    "Arterial_tortuosity_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Bicuspid_aortic_valve|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome|not_specified": 2,
    "Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiovascular_phenotype": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome|not_specified": 1,
    "Thoracic_aortic_aneurysm_or_dissection|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 1,
    "SLC2A10-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Aortic_aneurysm|_familial_thoracic_2|Arterial_tortuosity_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Arterial_tortuosity_syndrome|not_provided": 1,
    "Familial_aortopathy|Arterial_tortuosity_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Arterial_tortuosity_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_provided|not_specified|Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Arterial_tortuosity_syndrome|not_specified": 1,
    "not_specified|SLC2A10-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 1,
    "SLC2A10-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Arterial_tortuosity_syndrome": 1,
    "not_provided|Arterial_tortuosity_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Arterial_tortuosity_syndrome": 2,
    "ZMYND8-related_disorder": 4,
    "not_specified|ZMYND8-related_disorder": 1,
    "ZMYND8-related_disorder|ZMYND8-associated_neurodevelopmental_disorder": 1,
    "PREX1-related_disorder": 5,
    "not_provided|PREX1-related_disorder": 1,
    "not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 13,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_provided": 17,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|ARFGEF2-related_disorder|not_provided": 1,
    "ARFGEF2-related_disorder|not_specified": 4,
    "not_provided|ARFGEF2-related_disorder": 5,
    "not_specified|not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 7,
    "ARFGEF2-related_disorder|not_provided": 6,
    "not_provided|Microcephaly|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_specified": 5,
    "not_specified|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "Global_developmental_delay|Seizure|Hydrocephalus|not_provided": 1,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_specified|not_provided": 5,
    "not_provided|ARFGEF2-related_disorder|not_specified": 1,
    "ARFGEF2-related_disorder": 10,
    "ARFGEF2-related_disorder|not_specified|not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|Inborn_genetic_diseases|not_provided": 2,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_provided|ARFGEF2-related_disorder": 3,
    "not_specified|not_provided|ARFGEF2-related_disorder": 1,
    "ARFGEF2-related_disorder|not_specified|not_provided": 3,
    "ARFGEF2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|ARFGEF2-related_disorder|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_specified": 1,
    "not_specified|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_provided": 2,
    "not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|ARFGEF2-related_disorder": 1,
    "Periventricular_laminar_heterotopia": 5,
    "Inborn_genetic_diseases|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 2,
    "Intellectual_disability|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "not_provided|not_specified|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "not_provided|not_specified|ARFGEF2-related_disorder": 1,
    "not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_specified|ARFGEF2-related_disorder": 1,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|ARFGEF2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|Intellectual_disability|ARFGEF2-related_disorder|not_provided": 1,
    "not_specified|not_provided|ARFGEF2-related_disorder|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "Inborn_genetic_diseases|not_provided|Periventricular_heterotopia_with_microcephaly|_autosomal_recessive": 1,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability": 1,
    "Periventricular_laminar_heterotopia|Inborn_genetic_diseases|not_provided": 1,
    "Periventricular_heterotopia_with_microcephaly|_autosomal_recessive|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Periventricular_laminar_heterotopia": 1,
    "ZNFX1-related_disorder": 6,
    "Immunodeficiency_91_and_hyperinflammation": 15,
    "Immunodeficiency_91_and_hyperinflammation|Inborn_genetic_diseases": 1,
    "ZNFX1-related_disorder|not_provided": 3,
    "not_provided|ZNFX1-related_disorder": 2,
    "Inborn_genetic_diseases|Immunodeficiency_91_and_hyperinflammation": 1,
    "not_provided|not_specified|ZNFX1-related_disorder": 1,
    "Inborn_genetic_diseases|ZNFX1-related_disorder": 2,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_26": 3,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_26": 1,
    "Developmental_and_epileptic_encephalopathy|_26|Inborn_genetic_diseases": 9,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_26": 5,
    "not_provided|Developmental_and_epileptic_encephalopathy|_26": 27,
    "Developmental_and_epileptic_encephalopathy|_26|not_specified": 13,
    "Developmental_and_epileptic_encephalopathy|_26|not_provided": 51,
    "not_provided|Developmental_and_epileptic_encephalopathy|_26|Inborn_genetic_diseases": 3,
    "KCNB1-related_disorder|Developmental_and_epileptic_encephalopathy|_26|not_provided": 3,
    "KCNB1-related_disorder": 5,
    "Developmental_and_epileptic_encephalopathy|_26|not_specified|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_26|KCNB1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KCNB1-related_disorder|Developmental_and_epileptic_encephalopathy|_26": 7,
    "Developmental_and_epileptic_encephalopathy|_26|not_provided|Rare_genetic_intellectual_disability": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_26|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_26|not_provided|not_specified": 3,
    "See_cases|Developmental_and_epileptic_encephalopathy|_26|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_26|not_provided": 5,
    "Developmental_and_epileptic_encephalopathy|_26|Neurodevelopmental_abnormality": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_26|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_26": 2,
    "Developmental_and_epileptic_encephalopathy|_26|Intellectual_disability": 2,
    "not_provided|KCNB1-related_disorder|Developmental_and_epileptic_encephalopathy|_26": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_26": 1,
    "Inborn_genetic_diseases|KCNB1-related_disorder|Developmental_and_epileptic_encephalopathy|_26|not_provided": 1,
    "not_specified|KCNB1-related_disorder|Developmental_and_epileptic_encephalopathy|_26|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_26": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_26": 2,
    "not_provided|KCNB1-related_disorder|Developmental_and_epileptic_encephalopathy|_26|not_specified": 1,
    "not_provided|KCNB1-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_26": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_26|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_26|Epileptic_encephalopathy": 3,
    "Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_26": 3,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|_26": 1,
    "Developmental_and_epileptic_encephalopathy|_26|not_provided|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_26|Intellectual_disability|Epileptic_encephalopathy": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_26": 6,
    "KCNB1-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_26|Epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_26|Neurodevelopmental_delay": 1,
    "Developmental_and_epileptic_encephalopathy|_26|not_provided|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_delay|Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_26": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_26": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_26|Epileptic_encephalopathy|Seizure|Delayed_speech_and_language_development|Difficulty_walking|Intellectual_disability|Generalized_hypotonia|developmental_encephalopathy_with_epilepsy|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_26|not_provided|Intellectual_disability": 1,
    "developmental_encephalopathy_with_epilepsy|Developmental_and_epileptic_encephalopathy|_26|not_provided|Epilepsy|Myoclonic_absence_seizure|Epileptic_encephalopathy|Intellectual_disability": 1,
    "KCNB1-related_disorder|Inborn_genetic_diseases|not_provided|developmental_encephalopathy_with_epilepsy|Developmental_and_epileptic_encephalopathy|_26": 1,
    "Developmental_and_epileptic_encephalopathy|_26|KCNB1-related_disorder|not_provided": 1,
    "PTGIS-related_disorder": 4,
    "not_specified|Essential_hypertension|_genetic": 1,
    "not_provided|PTGIS-related_disorder": 1,
    "PTPN1-related_disorder|not_provided": 1,
    "not_provided|PTPN1-related_disorder": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided": 16,
    "ADNP-related_disorder|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ADNP-related_disorder|not_provided": 8,
    "not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 17,
    "not_provided|Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 4,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Intellectual_disability": 1,
    "ADNP-related_disorder": 10,
    "Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided": 12,
    "ADNP-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|ADNP-related_disorder": 2,
    "not_specified|not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|See_cases": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases|not_specified|not_provided|ADNP-related_disorder": 1,
    "Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|ADNP-related_disorder|not_provided": 2,
    "ADNP-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided": 1,
    "ADNP-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 2,
    "Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|ADNP-related_disorder|not_specified": 1,
    "not_provided|ADNP-related_disorder": 4,
    "See_cases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 1,
    "ADNP-related_disorder|Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided": 3,
    "not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_specified": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|Intellectual_disability": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|ADNP-related_disorder": 1,
    "Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 2,
    "See_cases|not_provided|Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 1,
    "ADNP-related_disorder|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|Inborn_genetic_diseases|ADNP-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Corpus_callosum|_agenesis_of|Decreased_response_to_growth_hormone_stimulation_test|Global_developmental_delay|Hypothyroidism|Stereotypic_movement_disorder|Abnormality_of_the_dentition|Seizure|Aggressive_behavior": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|ADNP-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|Intellectual_disability": 1,
    "ADNP-related_disorder|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases|not_provided": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases": 3,
    "ADNP-related_disorder|Intellectual_disability": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|ADNP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|ADNP-related_disorder": 1,
    "not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Inborn_genetic_diseases": 1,
    "not_provided|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|ADNP-related_disorder|Inborn_genetic_diseases": 1,
    "ADNP-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ADNP-related_disorder|not_provided": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_provided|ADNP-related_disorder|Inborn_genetic_diseases": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|Global_developmental_delay|not_provided|intellectual_deficiency|Autism|_severe": 1,
    "ADNP-related_disorder|Inborn_genetic_diseases|ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|not_specified|not_provided": 1,
    "not_provided|ADNP-related_disorder|Inborn_genetic_diseases": 1,
    "ADNP-related_multiple_congenital_anomalies_-_intellectual_disability_-_autism_spectrum_disorder|See_cases|not_provided": 1,
    "Congenital_disorder_of_glycosylation_type_1E": 184,
    "Congenital_disorder_of_glycosylation_type_1E|not_provided": 8,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|Congenital_disorder_of_glycosylation_type_1E": 1,
    "Congenital_disorder_of_glycosylation_type_1E|Inborn_genetic_diseases": 9,
    "DPM1-related_disorder|Congenital_disorder_of_glycosylation_type_1E": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation_type_1E": 1,
    "not_specified|Congenital_disorder_of_glycosylation_type_1E": 6,
    "Congenital_disorder_of_glycosylation_type_1E|not_specified|not_provided|Congenital_disorder_of_glycosylation": 1,
    "Congenital_disorder_of_glycosylation|DPM1-related_disorder|Congenital_disorder_of_glycosylation_type_1E|not_provided": 1,
    "Congenital_disorder_of_glycosylation_type_1E|not_specified|not_provided": 1,
    "not_provided|Congenital_disorder_of_glycosylation_type_1E|not_specified": 1,
    "Inborn_genetic_diseases|Congenital_disorder_of_glycosylation_type_1E": 4,
    "not_provided|Congenital_disorder_of_glycosylation_type_1E": 4,
    "DPM1-related_disorder": 2,
    "not_provided|DPM1-related_disorder": 1,
    "Congenital_disorder_of_glycosylation_type_1E|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_disorder_of_glycosylation_type_1E|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Congenital_disorder_of_glycosylation_type_1E|DPM1-related_disorder": 1,
    "DPM1-related_disorder|Congenital_disorder_of_glycosylation_type_1E|not_provided": 1,
    "not_provided|Congenital_disorder_of_glycosylation_type_1E|Inborn_genetic_diseases": 1,
    "Congenital_disorder_of_glycosylation_type_1E|not_specified": 1,
    "not_specified|not_provided|Congenital_disorder_of_glycosylation_type_1E": 1,
    "not_provided|not_specified|Congenital_disorder_of_glycosylation_type_1E": 1,
    "Inborn_genetic_diseases|not_provided|Congenital_disorder_of_glycosylation_type_1E": 1,
    "MOCS3-related_disorder|not_provided": 2,
    "not_provided|MOCS3-related_disorder": 3,
    "MOCS3-related_disorder": 1,
    "Joint_contractures|_osteochondromas|_and_B-cell_lymphoma": 2,
    "Neurodevelopmental_disorder_with_poor_growth_and_behavioral_abnormalities": 9,
    "Neurodevelopmental_disorder_with_poor_growth_and_behavioral_abnormalities|not_specified": 1,
    "Neurodevelopmental_disorder_with_poor_growth_and_behavioral_abnormalities|See_cases": 1,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome": 80,
    "not_provided|Duane-radial_ray_syndrome": 13,
    "not_provided|Oculootoradial_syndrome|Duane-radial_ray_syndrome": 2,
    "Duane-radial_ray_syndrome": 145,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome": 16,
    "Duane-radial_ray_syndrome|not_provided": 7,
    "SALL4-related_disorder|Inborn_genetic_diseases|not_provided|Duane-radial_ray_syndrome": 1,
    "SALL4-related_disorder|Inborn_genetic_diseases|Oculootoradial_syndrome|Duane-radial_ray_syndrome": 1,
    "Duane-radial_ray_syndrome|Inborn_genetic_diseases|Oculootoradial_syndrome": 2,
    "Inborn_genetic_diseases|Oculootoradial_syndrome|Duane-radial_ray_syndrome|not_provided": 1,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome|Inborn_genetic_diseases": 1,
    "Duane-radial_ray_syndrome|Inborn_genetic_diseases": 6,
    "SALL4-related_disorder": 16,
    "Inborn_genetic_diseases|Oculootoradial_syndrome|Duane-radial_ray_syndrome": 4,
    "SALL4-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Duane-radial_ray_syndrome|Oculootoradial_syndrome": 3,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Duane-radial_ray_syndrome|Oculootoradial_syndrome": 7,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome|SALL4-related_disorder": 1,
    "not_provided|not_specified|Duane-radial_ray_syndrome": 2,
    "Oculootoradial_syndrome": 2,
    "Duane-radial_ray_syndrome|not_specified|not_provided|SALL4-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Duane-radial_ray_syndrome|Oculootoradial_syndrome|not_provided": 2,
    "not_specified|Duane-radial_ray_syndrome|not_provided": 2,
    "not_specified|Duane-radial_ray_syndrome": 3,
    "not_provided|SALL4-related_disorder|Duane-radial_ray_syndrome|Oculootoradial_syndrome": 1,
    "SALL4-Related_Spectrum_Disorders": 1,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome|not_provided|not_specified": 5,
    "not_provided|Duane-radial_ray_syndrome|Oculootoradial_syndrome": 4,
    "SALL4-related_disorder|not_specified|not_provided|Duane-radial_ray_syndrome": 1,
    "not_provided|Duane-radial_ray_syndrome|not_specified": 1,
    "SALL4-related_disorder|Duane-radial_ray_syndrome|Oculootoradial_syndrome": 1,
    "SALL4-related_disorder|not_provided|Duane-radial_ray_syndrome": 3,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome|not_provided": 6,
    "Duane-radial_ray_syndrome|SALL4-related_disorder|not_provided": 1,
    "Duane-radial_ray_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Duane-radial_ray_syndrome|not_provided|not_specified": 1,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Duane-radial_ray_syndrome|SALL4-related_disorder": 2,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome|not_provided|SALL4-related_disorder": 1,
    "Inborn_genetic_diseases|Duane-radial_ray_syndrome|not_provided": 1,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome|SALL4-related_disorder": 5,
    "not_provided|SALL4-related_disorder": 1,
    "Duane-radial_ray_syndrome|not_provided|SALL4-related_disorder": 1,
    "Inborn_genetic_diseases|SALL4-related_disorder|not_provided|Duane-radial_ray_syndrome": 1,
    "not_specified|not_provided|Duane-radial_ray_syndrome|Oculootoradial_syndrome": 1,
    "Severe_combined_immunodeficiency|_autosomal_recessive|_T_cell-negative|_B_cell-negative|_NK_cell-positive|Duane-radial_ray_syndrome": 1,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Duane-radial_ray_syndrome": 1,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome|not_specified": 1,
    "SALL4-related_disorder|Duane-radial_ray_syndrome": 4,
    "SALL4-related_disorder|not_provided": 2,
    "Duane-radial_ray_syndrome|Oculootoradial_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "SALL4-related_disorder|Oculootoradial_syndrome|Duane-radial_ray_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Oculootoradial_syndrome|Duane-radial_ray_syndrome": 1,
    "Inborn_genetic_diseases|Duane-radial_ray_syndrome": 1,
    "not_specified|not_provided|Duane-radial_ray_syndrome": 1,
    "SALL4-related_disorder|not_specified|Duane-radial_ray_syndrome": 1,
    "Oculootoradial_syndrome|Duane-radial_ray_syndrome|not_specified": 1,
    "not_specified|Oculootoradial_syndrome|Duane-radial_ray_syndrome": 1,
    "not_provided|Infantile_hypercalcemia": 2,
    "Infantile_hypercalcemia": 4,
    "Hypercalcemia|_infantile|_1|not_provided": 37,
    "not_provided|Hypercalcemia|_infantile|_1": 24,
    "not_provided|Hypercalcemia|_infantile|_1|Inborn_genetic_diseases": 4,
    "Hypercalcemia|_infantile|_1|Inborn_genetic_diseases": 5,
    "CYP24A1-related_disorder": 3,
    "Inborn_genetic_diseases|Hypercalcemia|_infantile|_1|not_provided": 3,
    "Hypercalcemia|_infantile|_1|not_provided|CYP24A1-related_disorder": 3,
    "Hypercalcemia|_infantile|_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hypercalcemia|_infantile|_1|Inborn_genetic_diseases": 1,
    "Hypercalcemia|_infantile|_1|not_provided|Muscle_spasm|Inborn_genetic_diseases": 1,
    "Hypercalcemia|_infantile|_1|not_specified|not_provided": 3,
    "not_specified|Hypercalcemia|_infantile|_1": 1,
    "Hypercalcemia|_infantile|_1|not_provided|not_specified": 1,
    "Hypercalcemia|_infantile|_1|CYP24A1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Hypercalcemia|_infantile|_1": 1,
    "Inborn_genetic_diseases|not_provided|Hypercalcemia|_infantile|_1": 3,
    "CYP24A1-related_disorder|not_provided|Hypercalcemia|_infantile|_1": 2,
    "not_provided|Hypercalcemia|_infantile|_1|Inborn_genetic_diseases|not_specified": 1,
    "Hypercalcemia|_infantile|_1|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hypercalcemia|_infantile|_1": 1,
    "not_provided|Inborn_genetic_diseases|Hypercalcemia|_infantile|_1": 1,
    "MC3R-related_disorder": 71,
    "OBESITY_(BMIQ9)|_SUSCEPTIBILITY_TO": 3,
    "See_cases|MC3R-related_disorder": 1,
    "not_provided|MC3R-related_disorder": 6,
    "MC3R-related_disorder|not_provided": 7,
    "not_provided|not_specified|MC3R-related_disorder": 1,
    "not_specified|MC3R-related_disorder": 1,
    "AURKA-related_disorder": 4,
    "AURKA-related_disorder|Colon_cancer|_susceptibility_to|not_provided": 1,
    "BMP7-related_disorder": 8,
    "not_provided|Congenital_total_pulmonary_venous_return_anomaly|BMP7-related_disorder": 1,
    "not_provided|Atrial_septal_defect_8": 1,
    "BMP7-related_disorder|not_specified": 1,
    "not_provided|BMP7-related_disorder": 1,
    "BMP7-related_disorder|not_provided": 1,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic": 31,
    "PCK1-related_disorder|Inborn_genetic_diseases|not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic": 1,
    "not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic": 9,
    "Inborn_genetic_diseases|not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic": 2,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|not_provided": 26,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|Inborn_genetic_diseases": 1,
    "PCK1-related_disorder": 4,
    "Inborn_genetic_diseases|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic": 2,
    "not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|PCK1-related_disorder": 3,
    "not_provided|PCK1-related_disorder": 3,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|not_provided|Inborn_genetic_diseases": 1,
    "PCK1-related_disorder|Inborn_genetic_diseases|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|not_provided": 1,
    "Inborn_genetic_diseases|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|not_provided": 2,
    "PCK1-related_disorder|not_provided": 3,
    "Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|PCK1-related_disorder|not_provided": 1,
    "not_provided|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|PCK1-related_disorder": 1,
    "Lynch_syndrome_1|Inborn_genetic_diseases": 1,
    "PCK1-related_disorder|Inborn_genetic_diseases": 1,
    "PCK1-related_disorder|Phosphoenolpyruvate_carboxykinase_deficiency|_cytosolic|not_provided": 1,
    "Phosphoenolpyruvate_carboxykinase_(GTP)_deficiency|not_provided": 2,
    "Hereditary_disorder_of_connective_tissue": 1,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant": 137,
    "Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 132,
    "not_provided|Amyotrophic_Lateral_Sclerosis|_Dominant|Spinal_Muscular_Atrophy|_Dominant": 2,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|Spinal_Muscular_Atrophy|_Dominant": 14,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|not_provided": 5,
    "VAPB-related_disorder": 3,
    "Inborn_genetic_diseases|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 5,
    "Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|VAPB-related_disorder": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant": 9,
    "Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|not_provided": 9,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|not_provided|VAPB-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|VAPB-related_disorder": 1,
    "VAPB-related_disorder|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 2,
    "Amyotrophic_lateral_sclerosis_type_8|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant": 3,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Inborn_genetic_diseases": 7,
    "VAPB-related_disorder|Inborn_genetic_diseases|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 1,
    "Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|Inborn_genetic_diseases": 2,
    "not_provided|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 3,
    "not_provided|VAPB-related_disorder": 1,
    "not_provided|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|not_specified": 1,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|VAPB-related_disorder|not_specified|not_provided|Spinal_Muscular_Atrophy|_Dominant|Inborn_genetic_diseases": 1,
    "Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|not_provided|VAPB-related_disorder|Inborn_genetic_diseases": 1,
    "VAPB-related_disorder|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|VAPB-related_disorder|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 1,
    "not_provided|Inborn_genetic_diseases|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Amyotrophic_lateral_sclerosis_type_8": 1,
    "not_specified|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant": 1,
    "VAPB-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|not_specified|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|not_specified|Inborn_genetic_diseases": 1,
    "VAPB-related_disorder|Amyotrophic_lateral_sclerosis_type_8|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant|not_provided|Amyotrophic_lateral_sclerosis_type_8": 6,
    "not_provided|Spinal_Muscular_Atrophy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 2,
    "Spinal_Muscular_Atrophy|_Dominant|Amyotrophic_Lateral_Sclerosis|_Dominant": 2,
    "Amyotrophic_lateral_sclerosis_type_8|not_provided|Adult-onset_proximal_spinal_muscular_atrophy|_autosomal_dominant": 1,
    "Pseudohypoparathyroidism_type_1B|not_provided": 15,
    "not_provided|Pseudohypoparathyroidism_type_1B": 17,
    "Pseudohypoparathyroidism_type_1B|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Pseudohypoparathyroidism_type_1B": 2,
    "Pseudohypoparathyroidism_type_1B|not_provided|not_specified": 1,
    "STX16-related_disorder": 2,
    "not_specified|not_provided|Pseudohypoparathyroidism_type_1B": 1,
    "Inborn_genetic_diseases|Pseudohypoparathyroidism_type_1B|not_provided": 2,
    "Pseudohypoparathyroidism_type_1B|not_provided|Inborn_genetic_diseases": 2,
    "STX16-related_disorder|Inborn_genetic_diseases|not_provided|Pseudohypoparathyroidism_type_1B": 1,
    "GNAS-AS1-related_condition": 1,
    "GNAS-related_disorder": 328,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C": 1,
    "Pseudohypoparathyroidism_type_I_A": 37,
    "GNAS-related_disorder|not_specified": 8,
    "Pseudopseudohypoparathyroidism": 14,
    "GNAS-related_disorder|not_provided": 31,
    "Pseudohypoparathyroidism_type_I_A|not_specified": 1,
    "not_provided|GNAS-related_disorder": 40,
    "Duane_retraction_syndrome|GNAS-related_disorder": 3,
    "Pseudohypoparathyroidism_type_1B|GNAS-related_disorder": 3,
    "not_specified|GNAS-related_disorder|not_provided": 1,
    "GNAS-related_disorder|not_specified|not_provided|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism": 4,
    "Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A": 1,
    "not_provided|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|GNAS-related_disorder": 1,
    "GNAS-related_disorder|not_specified|not_provided|Inborn_genetic_diseases|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome": 1,
    "Pseudopseudohypoparathyroidism|GNAS-related_disorder": 4,
    "Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome": 4,
    "not_provided|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism": 1,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|not_specified|not_provided": 2,
    "Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|GNAS-related_disorder|McCune-Albright_syndrome": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|not_specified|not_provided|Pseudohypoparathyroidism|GNAS-related_disorder": 1,
    "GNAS-related_disorder|not_specified|not_provided": 5,
    "Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|not_provided|GNAS-related_disorder": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|GNAS-related_disorder": 1,
    "Pseudohypoparathyroidism|Intellectual_disability": 1,
    "McCune-Albright_syndrome": 13,
    "not_specified|GNAS-related_disorder": 2,
    "not_specified|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudopseudohypoparathyroidism|GNAS-related_disorder": 1,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1": 1,
    "Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Progressive_osseous_heteroplasia|not_provided": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_1B|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A": 1,
    "Inborn_genetic_diseases|GNAS-related_disorder": 3,
    "not_provided|Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|GNAS-related_disorder": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|not_specified|not_provided": 1,
    "McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|not_provided|GNAS-related_disorder": 1,
    "Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|not_provided": 1,
    "Cushing_syndrome|Pseudohypoparathyroidism_type_1B|Progressive_osseous_heteroplasia|McCune-Albright_syndrome|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|Somatotroph_adenoma": 1,
    "Inborn_genetic_diseases|GNAS-related_disorder|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome": 1,
    "Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|not_provided": 1,
    "GNAS-related_disorder|not_provided|not_specified": 1,
    "not_provided|GNAS-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_1B|Progressive_osseous_heteroplasia|Pseudopseudohypoparathyroidism|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_I_A": 1,
    "Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|GNAS-related_disorder|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|Progressive_osseous_heteroplasia": 1,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|not_provided|not_specified": 2,
    "Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia": 1,
    "GNAS-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "GNAS-related_disorder|not_specified|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|not_provided": 1,
    "GNAS-related_disorder|not_provided|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome": 1,
    "GNAS-related_disorder|Pseudopseudohypoparathyroidism": 2,
    "not_provided|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome": 1,
    "Pseudohypoparathyroidism_type_1B|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Cushing_syndrome|Pseudohypoparathyroidism|Somatotroph_adenoma|not_specified|not_provided": 1,
    "GNAS-related_disorder|not_specified|not_provided|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism": 1,
    "not_provided|Duane_retraction_syndrome|Inborn_genetic_diseases": 1,
    "Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A": 1,
    "not_provided|not_specified|GNAS-related_disorder": 2,
    "Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism": 1,
    "not_provided|Disorders_of_GNAS_Inactivation": 1,
    "not_provided|Progressive_osseous_heteroplasia|Cushing_syndrome|Pseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism": 1,
    "GNAS-related_disorder|Inborn_genetic_diseases|Pseudohypoparathyroidism|Pseudopseudohypoparathyroidism|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|not_provided": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|GNAS-related_disorder|not_provided": 3,
    "Pseudohypoparathyroidism_type_1B|Obesity|Hypocalcemia|Tetany|Subcutaneous_nodule|Cognitive_impairment|Round_face|Short_stature|Brachydactyly|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|Cushing_syndrome|Pseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|McCune-Albright_syndrome|not_provided": 1,
    "GNAS-related_disorder|not_provided|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome": 1,
    "Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism": 5,
    "not_provided|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia": 1,
    "Albright_hereditary_osteodystrophy|_pseudohypoparathyroidism|_pseudopseudohypoparathyroidism|_acrodysostosis_and_osteoma_cutis": 1,
    "GNAS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Pseudohypoparathyroidism_type_I_A|GNAS-related_disorder|not_provided": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|GNAS-related_disorder": 3,
    "Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Progressive_osseous_heteroplasia|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism": 1,
    "Progressive_osseous_heteroplasia": 2,
    "not_provided|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome": 4,
    "not_provided|not_specified|Pseudohypoparathyroidism_type_1B": 1,
    "Pseudohypoparathyroidism_type_1C": 6,
    "Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|not_provided|GNAS-related_disorder": 1,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1": 6,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Pseudohypoparathyroidism_type_I_A": 1,
    "not_provided|GNAS-associated_disease": 1,
    "not_provided|Pseudopseudohypoparathyroidism": 1,
    "GNAS-related_disorder|not_provided|Pseudohypoparathyroidism_type_I_A|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism": 1,
    "not_provided|Pseudohypoparathyroidism|Progressive_osseous_heteroplasia": 2,
    "not_provided|Pseudohypoparathyroidism|Pseudopseudohypoparathyroidism": 1,
    "Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|not_provided": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|not_provided|not_specified|Pseudohypoparathyroidism": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|McCune-Albright_syndrome": 2,
    "Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|GNAS-related_disorder|not_provided|not_specified": 1,
    "Pseudohypoparathyroidism_type_I_A|not_provided": 2,
    "not_specified|Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|not_provided|Pseudohypoparathyroidism_type_1B": 1,
    "Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C": 1,
    "not_provided|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1C|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|not_specified": 1,
    "not_provided|Pseudopseudohypoparathyroidism|Inborn_genetic_diseases": 1,
    "Pseudohypoparathyroidism_type_1C|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudopseudohypoparathyroidism|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome": 1,
    "not_provided|GNAS-related_disorder|Pseudohypoparathyroidism_type_I_A": 1,
    "not_provided|Pseudohypoparathyroidism_type_I_A": 4,
    "Pseudohypoparathyroidism_type_I_A|not_provided|Hereditary_spastic_paraplegia_4|Pseudohypoparathyroidism": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A": 1,
    "Inborn_genetic_diseases|not_provided|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|GNAS-related_disorder": 1,
    "Progressive_osseous_heteroplasia|McCune-Albright_syndrome|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_1C|Disorders_of_GNAS_Inactivation|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|GNAS-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "PHP_Type_1a_/_PPHP": 1,
    "not_provided|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_1C|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|not_specified": 1,
    "not_provided|GNAS-related_disorder|not_specified": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_1B|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1": 1,
    "ACTH-independent_macronodular_adrenal_hyperplasia_1|PITUITARY_TUMOR_3|_GROWTH_HORMONE-SECRETING|_SOMATIC|McCune-Albright_syndrome|Polyostotic_fibrous_dysplasia|_somatic|_mosaic": 1,
    "ACTH-independent_macronodular_adrenal_hyperplasia_1|Pituitary_adenoma_3|_multiple_types|not_provided|McCune-Albright_syndrome|Sex_cord-stromal_tumor|Pseudohypoparathyroidism_type_1B": 1,
    "Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|Progressive_osseous_heteroplasia|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C|Inborn_genetic_diseases|not_provided|Sex_cord-stromal_tumor": 1,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|McCune-Albright_syndrome|not_provided": 1,
    "Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome": 1,
    "Pituitary_adenoma_3|_multiple_types": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_I_A|not_provided|Pseudohypoparathyroidism_type_1B": 1,
    "not_provided|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Inborn_genetic_diseases|not_provided|McCune-Albright_syndrome|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pituitary_adenoma_3|_multiple_types|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism": 1,
    "not_provided|Pseudohypoparathyroidism|GNAS-related_disorder|Pseudohypoparathyroidism_type_I_A": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A": 1,
    "Progressive_osseous_heteroplasia|Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism": 1,
    "GNAS-related_disorder|not_provided|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_1B|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism": 1,
    "Pseudopseudohypoparathyroidism|not_provided": 1,
    "Pseudopseudohypoparathyroidism|Pseudohypoparathyroidism_type_I_A|not_provided|Inborn_genetic_diseases": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_I_A|not_provided": 1,
    "Disorders_of_GNAS_Inactivation": 1,
    "Pseudopseudohypoparathyroidism|Inborn_genetic_diseases": 1,
    "GNAS-related_disorder|Pseudohypoparathyroidism_type_I_A": 1,
    "Pseudohypoparathyroidism|Pseudohypoparathyroidism_type_1C": 1,
    "Pseudohypoparathyroidism_type_I_A|GNAS-related_disorder": 1,
    "not_specified|not_provided|McCune-Albright_syndrome|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|GNAS-related_disorder": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|ACTH-independent_macronodular_adrenal_hyperplasia_1|McCune-Albright_syndrome|Pituitary_adenoma_3|_multiple_types|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|not_specified|not_provided": 1,
    "Albright_hereditary_osteodystrophy|_pseudohypoparathyroidism|_pseudopseudohypoparathyroidism|_acrodysostosis_and_osteoma_cutis|GNAS-related_disorder|Pseudohypoparathyroidism_type_1B|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|McCune-Albright_syndrome|not_provided": 1,
    "Pseudohypoparathyroidism_type_1C|not_provided|Pseudohypoparathyroidism_type_I_A": 1,
    "PSEUDOHYPOPARATHYROIDISM|_TYPE_IA|_WITH_TESTOTOXICOSIS": 1,
    "Pseudohypoparathyroidism|not_provided": 1,
    "Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A|Progressive_osseous_heteroplasia|McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pituitary_adenoma_3|_multiple_types|Pseudopseudohypoparathyroidism|ACTH-independent_macronodular_adrenal_hyperplasia_1|not_provided": 1,
    "McCune-Albright_syndrome|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism|Progressive_osseous_heteroplasia|Pituitary_adenoma_3|_multiple_types|ACTH-independent_macronodular_adrenal_hyperplasia_1|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1C|not_provided": 1,
    "Pseudohypoparathyroidism_type_1B|McCune-Albright_syndrome": 1,
    "Pseudohypoparathyroidism_type_1C|Progressive_osseous_heteroplasia|Pseudohypoparathyroidism_type_I_A|Pseudohypoparathyroidism_type_1B|Pseudopseudohypoparathyroidism": 1,
    "not_provided|Pseudohypoparathyroidism_type_1C|Pseudohypoparathyroidism_type_I_A": 1,
    "not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant": 9,
    "Thrombocytopenia|Abnormal_bleeding|not_specified": 1,
    "Macrothrombocytopenia|_isolated|_1|_autosomal_dominant": 21,
    "not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|Thrombocytopenia|Abnormal_bleeding": 1,
    "Congenital_hypothyroidism|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|TUBB1-related_disorder|not_provided": 1,
    "TUBB1-related_disorder|not_specified": 1,
    "TUBB1-related_disorder|not_provided": 6,
    "not_provided|TUBB1-related_disorder": 7,
    "Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|not_provided": 2,
    "Macrothrombocytopenia|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|not_provided": 2,
    "not_specified|not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant": 3,
    "Macrothrombocytopenia|TUBB1-related_disorder|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|Thrombocytopenia|not_provided|not_specified": 1,
    "not_provided|not_specified|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant": 1,
    "Macrothrombocytopenia|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|not_specified|not_provided": 1,
    "TUBB1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|Inborn_genetic_diseases": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 61,
    "TUBB1-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|Thrombocytopenia|Abnormal_bleeding": 1,
    "Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|TUBB1-related_disorder|not_provided": 1,
    "not_specified|TUBB1-related_disorder": 1,
    "Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|not_provided|TUBB1-related_disorder": 1,
    "TUBB1-related_disorder|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|not_provided": 1,
    "TUBB1-related_disorder": 2,
    "Macrothrombocytopenia|not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant": 1,
    "Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|TUBB1-related_disorder": 1,
    "Macrothrombocytopenia|_isolated|_1|_autosomal_dominant|Thrombocytopenia|Abnormal_bleeding": 1,
    "TUBB1-related_disorder|not_specified|not_provided|Macrothrombocytopenia|_isolated|_1|_autosomal_dominant": 1,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_3": 2,
    "not_provided|ATP5F1E-related_disorder": 1,
    "ATP5F1E-related_disorder": 1,
    "Hirschsprung_Disease|_Dominant|not_provided|not_specified": 1,
    "Hirschsprung_disease|_susceptibility_to|_4": 52,
    "not_provided|Hirschsprung_disease|_susceptibility_to|_4": 3,
    "Hirschsprung_disease|_susceptibility_to|_4|not_provided": 5,
    "Hirschsprung_disease|_susceptibility_to|_4|Waardenburg_syndrome_type_4B|not_provided": 2,
    "Hirschsprung_disease|_susceptibility_to|_4|not_specified|not_provided": 1,
    "not_provided|EDN3-related_disorder|Abnormal_rectum_morphology|Megacolon|Hirschsprung_disease|_susceptibility_to|_4|Waardenburg_syndrome_type_4B": 1,
    "EDN3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|EDN3-related_disorder": 1,
    "EDN3-related_disorder": 4,
    "EDN3-related_disorder|Inborn_genetic_diseases": 1,
    "Waardenburg_syndrome_type_4B": 8,
    "EDN3-related_disorder|Waardenburg_syndrome_type_4B|Hirschsprung_disease|_susceptibility_to|_4": 1,
    "Hirschsprung_disease|_susceptibility_to|_4|Waardenburg_syndrome_type_4B|not_specified|not_provided": 1,
    "not_provided|not_specified|Hirschsprung_disease|_susceptibility_to|_4": 1,
    "Aganglionic_megacolon|Congenital_central_hypoventilation|Hirschsprung_Disease|_Dominant|not_provided|EDN3-related_disorder|not_specified|Waardenburg_syndrome_type_4B": 1,
    "not_provided|EDN3-related_disorder": 1,
    "Waardenburg_syndrome_type_4B|Hirschsprung_disease|_susceptibility_to|_4": 1,
    "Waardenburg_syndrome_type_4B|not_specified|Hirschsprung_disease|_susceptibility_to|_4|not_provided": 1,
    "Hirschsprung_disease|_susceptibility_to|_4|Inborn_genetic_diseases|not_provided": 1,
    "Hirschsprung_Disease|_Dominant|Waardenburg_syndrome": 4,
    "Hirschsprung_Disease|_Dominant|Waardenburg_syndrome|not_provided": 1,
    "SYCP2-related_disorder|not_provided": 1,
    "Spermatocyte_maturation_arrest|Oligosynaptic_infertility|Non-obstructive_azoospermia": 1,
    "Cryptozoospermia|Oligosynaptic_infertility|Non-obstructive_azoospermia": 2,
    "Oligosynaptic_infertility": 2,
    "SYCP2-related_disorder": 1,
    "CDH4-associated_disorder_of_corticaldevelopment": 1,
    "CDH4-related_disorder": 19,
    "Simplified_gyral_pattern": 2,
    "not_specified|CDH4-related_disorder|not_provided": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_73": 14,
    "Neurodevelopmental_disorder|Intellectual_developmental_disorder|_autosomal_dominant_73": 1,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_autosomal_dominant_73": 1,
    "Intellectual_developmental_disorder|_autosomal_dominant_73|Inborn_genetic_diseases": 1,
    "PSMA7-related_disorder": 1,
    "not_provided|SS18L1-related_disorder": 3,
    "SS18L1-related_disorder": 4,
    "SS18L1-related_disorder|not_provided": 3,
    "SS18L1-related_disorder|Amyotrophic_lateral_sclerosis|not_provided": 1,
    "OSBPL2-related_disorder": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_67|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_67": 6,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_67": 2,
    "OSBPL2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "OSBPL2-related_disorder|not_provided": 3,
    "not_provided|OSBPL2-related_disorder": 3,
    "not_specified|not_provided|OSBPL2-related_disorder": 3,
    "OSBPL2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_67|not_specified|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_67": 1,
    "not_specified|OSBPL2-related_disorder|not_provided": 1,
    "not_provided|LAMA5-related_disorder": 76,
    "LAMA5-related_disorder|not_specified|not_provided": 1,
    "LAMA5-related_disorder": 102,
    "LAMA5-related_disorder|not_provided": 98,
    "LAMA5-related_disorder|Inborn_genetic_diseases|not_provided": 13,
    "Nephrotic_syndrome|_IIa_26|not_provided": 1,
    "not_provided|LAMA5-related_disorder|Inborn_genetic_diseases": 6,
    "Nephrotic_syndrome|_IIa_26": 22,
    "not_provided|Polymicrogyria": 1,
    "Bent_bone_dysplasia_syndrome_2": 1,
    "LAMA5-related_disorder|Inborn_genetic_diseases": 4,
    "LAMA5-related_disorder|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|LAMA5-related_disorder|not_provided": 6,
    "LAMA5-related_disorder|Short_stature|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|LAMA5-related_disorder": 4,
    "not_provided|Inborn_genetic_diseases|LAMA5-related_disorder": 3,
    "Nephrotic_syndrome|_IIa_26|LAMA5-related_disorder|Inborn_genetic_diseases|Nephrotic_syndrome|not_provided": 1,
    "Nephrotic_syndrome|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|LAMA5-related_disorder": 7,
    "not_provided|Presynaptic_congenital_myasthenic_syndrome": 1,
    "LAMA5-related_disorder|Polymicrogyria|not_provided": 1,
    "not_provided|not_specified|LAMA5-related_disorder": 2,
    "LAMA5-related_disorder|Inborn_genetic_diseases|Nephrotic_syndrome": 1,
    "not_specified|not_provided|LAMA5-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Short_stature": 1,
    "Bent_bone_dysplasia_syndrome_2|LAMA5-related_disorder|not_provided": 1,
    "not_provided|distinct_bent_bone_dysplasia": 1,
    "Nephrotic_syndrome|_IIa_26|not_provided|Short_stature|Inborn_genetic_diseases": 1,
    "Severe_hydrocephalus|Holoprosencephaly_sequence|not_provided": 1,
    "Severe_hydrocephalus|Holoprosencephaly_sequence": 1,
    "Inborn_genetic_diseases|Nephrotic_syndrome|_IIa_26": 1,
    "Inborn_genetic_diseases|Multiple_sclerosis|not_provided": 1,
    "Macroscopic_hematuria": 1,
    "not_provided|Bent_bone_dysplasia_syndrome_2|distinct_bent_bone_dysplasia": 1,
    "Inborn_genetic_diseases|Multiple_sclerosis": 1,
    "Familial_hematuria|LAMA5-related_disorder|not_provided": 1,
    "Nephrotic_syndrome|_IIa_26|Nephrotic_syndrome": 2,
    "LAMA5-related_disorder|Nephrotic_syndrome|_IIa_26": 1,
    "Short_stature|Inborn_genetic_diseases": 1,
    "Congenital_omphalocele|Nephrotic_syndrome|_IIa_26": 1,
    "Inborn_genetic_diseases|LAMA5-related_multisystemic_syndrome": 1,
    "GATA5-related_disorder|not_provided": 5,
    "not_provided|Congenital_heart_defects|_multiple_types|_5|not_specified": 2,
    "not_provided|GATA5-related_disorder": 8,
    "GATA5-related_disorder": 3,
    "not_provided|Aortic_valve_disease_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Congenital_heart_defects|_multiple_types|_5|not_provided|not_specified": 2,
    "Congenital_heart_defects|_multiple_types|_5|not_provided": 3,
    "not_specified|Congenital_heart_defects|_multiple_types|_5|not_provided": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|GATA5-related_disorder": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_5": 4,
    "Congenital_heart_defects|_multiple_types|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_5|not_specified|not_provided": 1,
    "Congenital_heart_defects|_multiple_types|_5": 7,
    "not_specified|GATA5-related_disorder": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_5|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Congenital_heart_defects|_multiple_types|_5": 1,
    "GATA5-related_disorder|not_provided|not_specified": 2,
    "GATA5-related_disorder|not_provided|Congenital_heart_defects|_multiple_types|_5": 1,
    "Congenital_heart_defects|_multiple_types": 1,
    "Arterial_dissection|not_provided": 1,
    "not_provided|GATA5-related_disorder|Congenital_heart_defects|_multiple_types|_5": 1,
    "not_provided|Congenital_heart_defects|_multiple_types|_5|GATA5-related_disorder": 1,
    "GATA5-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|COL9A3-related_disorder": 19,
    "COL9A3-related_disorder|not_provided": 23,
    "not_specified|not_provided|Epiphyseal_dysplasia|_multiple|_3|Connective_tissue_disorder": 1,
    "not_specified|Epiphyseal_dysplasia|_multiple|_3|not_provided": 3,
    "Autosomal_recessive_Stickler_syndrome|Epiphyseal_dysplasia|_multiple|_3|not_provided": 2,
    "COL9A3-related_disorder|not_specified|not_provided": 6,
    "Stickler_syndrome|_type_6|not_provided": 2,
    "Epiphyseal_dysplasia|_multiple|_3": 11,
    "COL9A3-related_disorder|not_provided|Epiphyseal_dysplasia|_multiple|_3|Epiphyseal_dysplasia|_multiple|_3|_with_myopathy": 1,
    "Epiphyseal_dysplasia|_multiple|_3|not_provided": 3,
    "not_provided|Connective_tissue_disorder|COL9A3-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|Stickler_syndrome": 1,
    "Epiphyseal_dysplasia|_multiple|_3|Stickler_syndrome|_type_6|Intervertebral_disc_disorder|not_provided": 1,
    "not_specified|COL9A3-related_disorder|not_provided": 1,
    "Stickler_syndrome|not_provided|Stickler_syndrome|_type_6": 1,
    "Stickler_syndrome|Connective_tissue_disorder|Intervertebral_disc_disease|_susceptibility_to|not_provided|not_specified": 1,
    "not_provided|Intervertebral_disc_disorder|Epiphyseal_dysplasia|_multiple|_3": 4,
    "not_specified|not_provided|COL9A3-related_disorder": 1,
    "Stickler_syndrome|_type_6": 4,
    "not_provided|Epiphyseal_dysplasia|_multiple|_3": 1,
    "not_provided|Intervertebral_disc_disorder|Epiphyseal_dysplasia|_multiple|_3|Stickler_syndrome|_type_6": 1,
    "COL9A3-related_disorder|Connective_tissue_disorder|not_provided|Epiphyseal_dysplasia|_multiple|_3|Lattice_retinal_degeneration|Retinal_detachment|Intervertebral_disc_disorder": 1,
    "not_provided|COL9A3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Stickler_syndrome|_type_6|Epiphyseal_dysplasia|_multiple|_3|Connective_tissue_disorder": 1,
    "COL9A3-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|COL9A3-related_disorder": 2,
    "Intervertebral_disc_disorder|Epiphyseal_dysplasia|_multiple|_3|not_provided": 1,
    "not_provided|not_specified|Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|Connective_tissue_disorder": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_3|Vitreoretinopathy|Intervertebral_disc_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_Stickler_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Epiphyseal_dysplasia|_multiple|_3": 2,
    "not_specified|Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Multiple_Epiphyseal_Dysplasia|_Dominant|not_provided|Epiphyseal_dysplasia|_multiple|_3": 1,
    "Stickler_syndrome|_type_6|Epiphyseal_dysplasia|_multiple|_3|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_3|not_specified": 2,
    "Lattice_retinal_degeneration|Retinal_detachment": 1,
    "not_provided|Intervertebral_disc_disorder|Epiphyseal_dysplasia|_multiple|_3|Stickler_syndrome|_type_6|Inborn_genetic_diseases": 1,
    "not_provided|Stickler_syndrome|_type_6": 1,
    "COL9A3-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Connective_tissue_disorder|not_specified|Epiphyseal_dysplasia|_multiple|_3|not_provided": 1,
    "Stickler_syndrome|_type_6|Inborn_genetic_diseases|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_3|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|not_provided": 2,
    "Inborn_genetic_diseases|COL9A3-related_disorder|not_provided": 1,
    "not_provided|Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder": 1,
    "Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|not_provided": 2,
    "Deafness|Intervertebral_disc_disorder|Epiphyseal_dysplasia|_multiple|_3|Stickler_syndrome|_type_6|not_provided": 1,
    "Stickler_syndrome|not_provided|Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|Stickler_syndrome|_type_6": 1,
    "Inborn_genetic_diseases|Skeletal_dysplasia|not_provided": 1,
    "not_provided|not_specified|Epiphyseal_dysplasia|_multiple|_3": 1,
    "Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|Bilateral_sensorineural_hearing_impairment|not_provided": 1,
    "Intervertebral_disc_disorder|Stickler_syndrome|_type_6|Epiphyseal_dysplasia|_multiple|_3|not_provided": 1,
    "Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|Inborn_genetic_diseases|not_provided|COL9A3-related_disorder": 1,
    "Epiphyseal_dysplasia|_multiple|_3|Intervertebral_disc_disorder|Stickler_syndrome|_type_6|Inborn_genetic_diseases|not_provided": 1,
    "Multiple_Epiphyseal_Dysplasia|_Dominant": 2,
    "Oligoasthenoteratozoospermia": 3,
    "Porokeratosis_8|_disseminated_superficial_actinic_type|not_specified": 2,
    "SLC17A9-related_disorder": 11,
    "SLC17A9-related_disorder|not_provided": 5,
    "Porokeratosis_8|_disseminated_superficial_actinic_type": 3,
    "Disseminated_superficial_actinic_porokeratosis": 1,
    "Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 4,
    "not_provided|CHRNA4-related_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 6,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_specified": 1,
    "not_provided|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "CHRNA4-related_disorder": 4,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Seizure|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_addiction|_susceptibility_to": 1,
    "CHRNA4-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|Tobacco_use_disorder|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|NICOTINE_ADDICTION|_PROTECTION_AGAINST|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "Inborn_genetic_diseases|CHRNA4-related_disorder|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Frontotemporal_dementia": 1,
    "Inborn_genetic_diseases|NICOTINE_ADDICTION|_PROTECTION_AGAINST|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 1,
    "not_provided|Tobacco_use_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 10,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 5,
    "CHRNA4-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_specified": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided": 1,
    "CHRNA4-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 3,
    "Inborn_genetic_diseases|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "Tobacco_use_disorder": 9,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to": 2,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|not_provided": 3,
    "Inborn_genetic_diseases|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 3,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 1,
    "CHRNA4-related_disorder|Inborn_genetic_diseases|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Developmental_and_epileptic_encephalopathy_94|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided": 1,
    "CHRNA4-related_disorder|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA4-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 2,
    "Familial_sleep-related_hypermotor_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Inborn_genetic_diseases": 1,
    "CHRNA4-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder": 3,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 2,
    "not_provided|Amyotrophic_lateral_sclerosis|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "not_provided|Inborn_genetic_diseases|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA4-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Inborn_genetic_diseases": 1,
    "Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA4-related_disorder": 1,
    "CHRNA4-related_disorder|Tobacco_use_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to|Inborn_genetic_diseases": 1,
    "CHRNA4-related_disorder|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_specified|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Amyotrophic_lateral_sclerosis": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|CHRNA4-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder": 1,
    "Tobacco_use_disorder|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|not_specified": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to": 1,
    "Amyotrophic_lateral_sclerosis|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_use_disorder|not_specified|not_provided": 1,
    "CHRNA4-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_provided": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified": 2,
    "CHRNA4-related_disorder|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 2,
    "CHRNA4-related_disorder|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1": 1,
    "not_provided|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_specified": 1,
    "not_provided|Tobacco_addiction|_susceptibility_to|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to|not_provided|not_specified": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|not_specified|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy_1|Tobacco_addiction|_susceptibility_to|not_specified|not_provided": 1,
    "CHRNA4-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|KCNQ2-related_disorder|not_provided": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_provided|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 17,
    "Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 1,
    "KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|not_specified": 1,
    "KCNQ2-related_disorder": 10,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7": 21,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7": 8,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Dystonia|_early-onset|_and/or_spastic_paraplegia|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Intellectual_disability|Continuous_spike_and_waves_during_slow_sleep": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy|not_provided": 6,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Inborn_genetic_diseases|KCNQ2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_7|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases": 1,
    "KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy": 5,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_7": 5,
    "Developmental_and_epileptic_encephalopathy|not_specified|See_cases": 2,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Seizure": 2,
    "KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder": 1,
    "not_provided|KCNQ2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_7|not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7": 3,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|not_specified|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_7": 2,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_provided|Inborn_genetic_diseases": 2,
    "KCNQ2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 3,
    "not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_neonatal|_1|Seizure": 2,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder": 7,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 12,
    "Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy": 15,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|not_provided": 3,
    "Benign_Rolandic_epilepsy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_7": 7,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 4,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy": 13,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_provided|Seizures|_benign_familial_neonatal|_1|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_provided|Seizures|_benign_familial_neonatal|_1|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_7|not_provided": 6,
    "Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_neonatal|_1": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_7": 1,
    "KCNQ2-related_disorder|Epilepsy|Developmental_and_epileptic_encephalopathy|not_provided|Seizure": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder|Limb_dystonia|Absent_speech|Global_developmental_delay|KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_2|Seizures|_benign_familial_neonatal|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided|Developmental_and_epileptic_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Inborn_genetic_diseases|Complex_neurodevelopmental_disorder": 1,
    "Seizures|_benign_familial_neonatal|_1|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided": 1,
    "KCNQ2-related_disorder|not_provided": 3,
    "not_specified|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided|Inborn_genetic_diseases": 1,
    "KCNQ2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy|not_provided": 2,
    "Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 1,
    "not_provided|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy": 4,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_provided|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|Seizure": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|KCNQ2-related_disorder|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases": 1,
    "KCNQ2-related_disorder|not_specified": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|KCNQ2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases": 1,
    "not_provided|KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|not_specified|KCNQ2-related_disorder|not_provided": 1,
    "Epilepsy|_benign_neonatal|_1|_and/or_myokymia|Seizures|_benign_familial_neonatal|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Seizures|_benign_familial_neonatal|_1|Seizure": 1,
    "Abnormal_facial_shape|Epicanthus|Seizure|Intellectual_disability|_moderate|Autistic_behavior|not_provided|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|_7|Seizure": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_provided|Autosomal_recessive_congenital_ichthyosis_10": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided|Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases": 1,
    "Benign_Rolandic_epilepsy|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Seizure|KCNQ2-related_disorder": 1,
    "Seizure|not_provided|Epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Seizure|Epileptic_encephalopathy": 1,
    "KCNQ2-related_disorder|Seizures|_benign_familial_neonatal|_1": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7|not_provided": 1,
    "Seizure|Generalized_hypotonia": 1,
    "KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Inborn_genetic_diseases|KCNQ2-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|West_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_1": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided|Epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_provided|Seizure|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_7|Seizure": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided": 2,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy": 3,
    "not_provided|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Seizure|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_specified": 1,
    "Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Seizures|_benign_familial_neonatal|_2|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Seizures|_benign_familial_neonatal|_1": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Seizure|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy|Seizures|_benign_familial_neonatal|_1": 1,
    "Inborn_genetic_diseases|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Neonatal/infantile_epilepsy_syndrome|Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_neonatal|_1": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizures|_benign_familial_neonatal|_1|Intellectual_disability|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|KCNQ2-related_disorder|Seizures|_benign_familial_neonatal|_1|_and/or_myokymia": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided|Seizures|_benign_familial_neonatal|_1|_and/or_myokymia|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided|Severe_intellectual_deficiency": 1,
    "Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided|See_cases": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Seizures|_benign_familial_neonatal|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_7|not_provided|KCNQ2-related_disorder|Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 2,
    "Developmental_and_epileptic_encephalopathy|Neonatal_encephalopathy": 1,
    "not_provided|Seizure|Developmental_and_epileptic_encephalopathy": 1,
    "KCNQ2-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_7|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_7|KCNQ2-related_disorder": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7|not_provided|Seizure": 1,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_7|Seizures|_benign_familial_neonatal|_1": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|KCNQ2-related_disorder": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|Developmental_and_epileptic_encephalopathy|not_provided|KCNQ2-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|Benign_neonatal_seizures": 1,
    "KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy|_7": 1,
    "not_provided|KCNQ2-related_disorder|Developmental_and_epileptic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_7": 1,
    "Seizures|_benign_familial_neonatal|_1|Developmental_and_epileptic_encephalopathy|_7|not_specified|Developmental_and_epileptic_encephalopathy": 1,
    "See_cases|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|not_provided": 1,
    "Seizures|_benign_familial_neonatal|_1|not_provided|Developmental_and_epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_33|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_33|not_provided|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_33|not_provided": 25,
    "Intellectual_disability|_autosomal_dominant_38": 8,
    "Developmental_and_epileptic_encephalopathy|_33|Intellectual_disability|_autosomal_dominant_38|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_33|not_specified": 11,
    "EEF1A2-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33": 5,
    "Developmental_and_epileptic_encephalopathy|_33|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_33": 21,
    "not_provided|Developmental_and_epileptic_encephalopathy|_33|not_specified|Inborn_genetic_diseases": 3,
    "not_provided|Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy": 1,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases": 10,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Congenital_heart_disease|Developmental_and_epileptic_encephalopathy|_33|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_33|not_specified": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33": 11,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|not_provided": 2,
    "EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy|Developmental_and_epileptic_encephalopathy|_33": 2,
    "Developmental_and_epileptic_encephalopathy|_33|not_provided|Intellectual_disability": 2,
    "Developmental_and_epileptic_encephalopathy|_33|Intellectual_disability|_autosomal_dominant_38": 3,
    "Intellectual_disability|not_specified|Developmental_and_epileptic_encephalopathy|_33|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases": 3,
    "Autism|Seizure|Global_developmental_delay|Developmental_and_epileptic_encephalopathy|_33": 1,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33|not_specified|not_provided": 3,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases|EEF1A2-related_disorder|not_provided|EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_33|EEF1A2-related_disorder": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_33": 3,
    "EEF1A2-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_33": 1,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_33|Intellectual_disability|_autosomal_dominant_38|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|EEF1A2-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|EEF1A2-related_disorder|Developmental_and_epileptic_encephalopathy|_33|not_provided": 1,
    "Autosomal_dominant_epilepsy|Developmental_and_epileptic_encephalopathy|_33": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33|not_specified|EEF1A2-related_disorder": 1,
    "not_specified|EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy": 1,
    "Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|not_provided|EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33|not_provided|EEF1A2-related_disorder": 1,
    "EEF1A2-related_disorder|Developmental_and_epileptic_encephalopathy|_33": 1,
    "Hereditary_spastic_paraplegia_46|Developmental_and_epileptic_encephalopathy|_33": 1,
    "EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy": 1,
    "EEF1A2-related_disorder": 3,
    "Developmental_and_epileptic_encephalopathy|_33|Intellectual_disability|_autosomal_dominant_38|not_provided|EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy": 1,
    "EEF1A2-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|EEF1A2-related_disorder|Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|not_provided|EEF1A2-related_developmental_and_degenerative_epileptic-dyskinetic_encephalopathy|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_33|not_specified": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_38|Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases|not_specified": 1,
    "EEF1A2-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_33": 1,
    "Inborn_genetic_diseases|not_provided|EEF1A2-related_disorder|Developmental_and_epileptic_encephalopathy|_33": 1,
    "EEF1A2-related_disorder|Developmental_and_epileptic_encephalopathy|_33|Inborn_genetic_diseases|Intellectual_disability|_autosomal_dominant_38|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 829,
    "RTEL1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 11,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 8,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 240,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 16,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 34,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 126,
    "not_provided|RTEL1-related_disorder|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 971,
    "Dyskeratosis_congenita|_autosomal_recessive_1|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 199,
    "RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 5,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 22,
    "not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 7,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 147,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 10,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Inborn_genetic_diseases": 9,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided": 24,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 7,
    "Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "not_provided|not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita": 4,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|Dyskeratosis_congenita": 11,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 20,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_1|not_specified|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 5,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_specified": 1,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 18,
    "Dyskeratosis_congenita|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 9,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Pulmonary_fibrosis": 4,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 18,
    "not_provided|not_specified|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 27,
    "RTEL1-related_disorder": 11,
    "Dyskeratosis_congenita|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|Inborn_genetic_diseases|not_specified": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided": 5,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|RTEL1-related_disorder|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|not_provided|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita": 4,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 9,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 4,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_provided": 3,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 5,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|not_provided|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 2,
    "not_specified|Dyskeratosis_congenita|not_provided|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Inborn_genetic_diseases|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 6,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|Inborn_genetic_diseases": 3,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|Inborn_genetic_diseases": 10,
    "Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_1|not_specified|Dyskeratosis_congenita|not_provided": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Dyskeratosis_congenita": 4,
    "not_provided|Dyskeratosis_congenita|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 17,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 6,
    "Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "not_provided|Dyskeratosis_congenita|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "not_provided|RTEL1-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_specified": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided": 6,
    "RTEL1-related_disorder|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|Dyskeratosis_congenita": 12,
    "not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder|not_provided": 2,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|not_specified": 1,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 4,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 6,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|not_specified|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1": 2,
    "RTEL1-related_disorder|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 2,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|RTEL1-related_disorder": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 3,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Acute_myeloid_leukemia": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 5,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|_autosomal_recessive_1|Dyskeratosis_congenita|_X-linked|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 1,
    "RTEL1-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Inborn_genetic_diseases": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|RTEL1-related_disorder": 1,
    "not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified": 4,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Dyskeratosis_congenita|_X-linked": 40,
    "not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita": 2,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|Inborn_genetic_diseases": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 2,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 4,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Interstitial_lung_disease_2": 1,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|RTEL1-related_disorder": 2,
    "not_provided|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "RTEL1-related_disorder|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_specified|not_provided|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|RTEL1-related_disorder": 2,
    "Dyskeratosis_congenita|_autosomal_dominant_4": 1,
    "Inborn_genetic_diseases|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis": 1,
    "Pulmonary_fibrosis|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 2,
    "Dyskeratosis_congenita|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 4,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_provided|not_specified": 1,
    "Dyskeratosis_congenita|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Pulmonary_fibrosis": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|RTEL1-related_disorder": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided": 9,
    "Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 3,
    "Dyskeratosis_congenita|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Telomere_syndrome": 1,
    "Dyskeratosis_congenita|not_provided|not_specified|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 11,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|Dyskeratosis_congenita|not_provided": 1,
    "not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 2,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Inborn_genetic_diseases": 3,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|Dyskeratosis_congenita|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Interstitial_lung_disease_2": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Telomere_syndrome": 1,
    "Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Combined_oxidative_phosphorylation_defect_type_24|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "not_provided|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|not_specified|not_provided": 2,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 3,
    "RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Dyskeratosis_congenita|not_provided": 1,
    "RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder": 5,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|Dyskeratosis_congenita|not_provided": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|not_provided": 1,
    "not_specified|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|not_specified|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "RTEL1-related_disorder|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_1|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|not_provided": 3,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|not_specified": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Inborn_genetic_diseases|not_specified|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|RTEL1-related_disorder|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided": 1,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|RTEL1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|RTEL1-related_disorder": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_provided|Inborn_genetic_diseases": 3,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|Inborn_genetic_diseases|not_specified": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 4,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "not_specified|Dyskeratosis_congenita|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "RTEL1-related_disorder|not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Pulmonary_fibrosis|not_provided|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_specified|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|Pulmonary_fibrosis|Dyskeratosis_congenita|_autosomal_dominant_4|not_provided|Adams-Oliver_syndrome_3|Dyskeratosis_congenita": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|Interstitial_lung_disease_2": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|RTEL1-related_disorder|not_provided|Dyskeratosis_congenita": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|Dyskeratosis_congenita": 2,
    "RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|Dyskeratosis_congenita|not_specified": 1,
    "Dyskeratosis_congenita|RTEL1-related_disorder|not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|Inborn_genetic_diseases": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_dominant_1|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|not_specified": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Microcephaly|not_provided": 1,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|not_provided": 1,
    "not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|Dyskeratosis_congenita": 2,
    "Dyskeratosis_congenita|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|not_specified": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|not_provided": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Abnormality_of_blood_and_blood-forming_tissues": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|RTEL1-related_disorder|not_specified": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder|not_provided|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder|Inborn_genetic_diseases": 2,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|RTEL1-related_disorder": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder|Dyskeratosis_congenita": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|Microcephaly": 1,
    "RTEL1-related_disorder|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 2,
    "Inborn_genetic_diseases|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Pulmonary_fibrosis": 1,
    "not_provided|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita": 1,
    "RTEL1-related_disorder|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_specified": 1,
    "Dyskeratosis_congenita|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided": 1,
    "not_specified|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_autosomal_recessive_5|RTEL1-related_disorder|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|RTEL1-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Inborn_genetic_diseases|not_provided|Immunodeficiency|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|not_provided|Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Inborn_genetic_diseases|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_dominant_1|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|not_specified|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|Dyskeratosis_congenita": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|_autosomal_dominant_1|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_dominant_1": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Interstitial_lung_disease_2|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|Inborn_genetic_diseases|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3": 1,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|Inborn_genetic_diseases": 1,
    "Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|Dyskeratosis_congenita|_autosomal_recessive_5|Dyskeratosis_congenita|not_specified|Inborn_genetic_diseases": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|not_specified|RTEL1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|Dyskeratosis_congenita|_autosomal_recessive_5": 1,
    "Inborn_genetic_diseases|Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_provided|Dyskeratosis_congenita|Interstitial_lung_disease_2|See_cases": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|RTEL1-related_disorder|not_specified": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|Pulmonary_fibrosis_and/or_bone_marrow_failure|_Telomere-related|_3|not_specified|Inborn_genetic_diseases": 1,
    "TNFRSF6B-related_disorder": 3,
    "TNFRSF6B-related_disorder|not_provided": 7,
    "TNFRSF6B-related_disorder|not_provided|not_specified": 2,
    "TNFRSF6B-related_disorder|not_specified|not_provided": 2,
    "not_provided|TNFRSF6B-related_disorder": 4,
    "not_provided|Dyskeratosis_congenita|_autosomal_recessive_5": 3,
    "not_specified|Dyskeratosis_congenita|_autosomal_recessive_5|not_provided": 3,
    "not_specified|TNFRSF6B-related_disorder|not_provided": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|not_provided|not_specified|TNFRSF6B-related_disorder": 1,
    "Dyskeratosis_congenita|_autosomal_recessive_5|not_specified|not_provided": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 40,
    "Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|Neuronal_Ceroid-Lipofuscinosis|_Recessive": 27,
    "Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_provided": 9,
    "Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 42,
    "not_provided|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 4,
    "not_specified|Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|Neuronal_Ceroid-Lipofuscinosis|_Recessive": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_specified|not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_specified": 1,
    "not_provided|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Inborn_genetic_diseases|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Inborn_genetic_diseases|DNAJC5-related_disorder|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_specified": 1,
    "Neuronal_ceroid_lipofuscinosis|not_provided|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_specified": 1,
    "Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|Neuronal_ceroid_lipofuscinosis": 1,
    "DNAJC5-related_disorder|not_specified|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|not_specified|Neuronal_ceroid_lipofuscinosis|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_specified|not_provided|Neuronal_Ceroid-Lipofuscinosis|_Recessive": 1,
    "Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "not_provided|DNAJC5-related_disorder|Neuronal_ceroid_lipofuscinosis": 1,
    "DNAJC5-related_disorder|not_provided|Neuronal_ceroid_lipofuscinosis": 1,
    "Inborn_genetic_diseases|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|Neuronal_ceroid_lipofuscinosis": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 2,
    "Neuronal_ceroid_lipofuscinosis|Neuronal_Ceroid-Lipofuscinosis|_Recessive|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_provided": 1,
    "not_specified|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Inborn_genetic_diseases|not_provided|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Neuronal_ceroid_lipofuscinosis|DNAJC5-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|not_provided|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Inborn_genetic_diseases|Neuronal_ceroid_lipofuscinosis|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_provided": 1,
    "Neuronal_ceroid_lipofuscinosis|Inborn_genetic_diseases|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_provided": 13,
    "Neuronal_Ceroid-Lipofuscinosis|_Recessive|not_provided|Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)": 1,
    "Ceroid_lipofuscinosis|_neuronal|_4_(Kufs_type)|not_provided": 1,
    "ZNF512B-related_disorder": 21,
    "Retinitis_pigmentosa_60|Retinitis_pigmentosa|not_provided": 1,
    "PRPF6-related_disorder|not_provided": 6,
    "Retinitis_pigmentosa_60": 5,
    "not_provided|Retinitis_pigmentosa|PRPF6-related_disorder": 1,
    "Retinitis_pigmentosa|PRPF6-related_disorder|not_provided": 2,
    "PRPF6-related_disorder": 1,
    "Retinal_dystrophy|PRPF6-related_disorder|not_provided": 1,
    "not_provided|PRPF6-related_disorder": 5,
    "not_provided|Retinitis_pigmentosa_60": 1,
    "Retinitis_pigmentosa_60|not_provided": 1,
    "not_specified|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_60": 1,
    "Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome": 35,
    "Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|not_provided": 2,
    "SOX18-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome": 2,
    "Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome|not_provided": 3,
    "Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 2,
    "Inborn_genetic_diseases|Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 2,
    "not_provided|Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 3,
    "not_provided|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome": 3,
    "SOX18-related_disorder": 2,
    "Inborn_genetic_diseases|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome|not_provided": 2,
    "Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hypotrichosis-lymphedema-telangiectasia_syndrome|Inborn_genetic_diseases|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 1,
    "Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Inborn_genetic_diseases": 1,
    "Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|SOX18-related_disorder": 1,
    "Bladder_exstrophy-epispadias-cloacal_extrophy_complex|not_provided": 1,
    "Inborn_genetic_diseases|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome": 3,
    "not_provided|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 1,
    "not_provided|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome|Inborn_genetic_diseases": 2,
    "Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hypotrichosis-lymphedema-telangiectasia_syndrome": 1,
    "Hypotrichosis-lymphedema-telangiectasia_syndrome": 2,
    "not_provided|not_specified|Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 1,
    "Hypotrichosis-lymphedema-telangiectasia_syndrome|Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome": 1,
    "Hypotrichosis-lymphedema-telangiectasia-renal_defect_syndrome|Hypotrichosis-lymphedema-telangiectasia_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|SOX18-related_disorder": 1,
    "MYT1-related_disorder|not_provided": 7,
    "MYT1-related_disorder": 20,
    "not_provided|MYT1-related_disorder": 8,
    "Inborn_genetic_diseases|MYT1-related_disorder": 2,
    "U2AF1L5-related_condition": 1,
    "CRYAA2-related_condition": 2,
    "KCNE1B-related_condition": 1,
    "Macrocephaly|Autism_spectrum_disorder": 1,
    "not_provided|LIPI-related_disorder": 2,
    "LIPI-related_disorder": 1,
    "not_specified|not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_3": 1,
    "not_provided|NRIP1-related_disorder|Congenital_anomalies_of_kidney_and_urinary_tract_3": 1,
    "NRIP1-related_disorder": 19,
    "Congenital_anomalies_of_kidney_and_urinary_tract_3": 8,
    "NRIP1-related_disorder|not_provided": 14,
    "not_provided|NRIP1-related_disorder": 9,
    "NRIP1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_3|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|NRIP1-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|NRIP1-related_disorder": 2,
    "not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_3|NRIP1-related_disorder": 1,
    "Congenital_anomalies_of_kidney_and_urinary_tract_3|NRIP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|NRIP1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Congenital_anomalies_of_kidney_and_urinary_tract_3": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Congenital_anomalies_of_kidney_and_urinary_tract_3": 1,
    "not_provided|Congenital_anomalies_of_kidney_and_urinary_tract_3": 1,
    "Epilepsy|_idiopathic_generalized|_susceptibility_to|_19": 1,
    "Enterokinase_deficiency": 9,
    "Enterokinase_deficiency|not_provided": 4,
    "TMPRSS15-related_disorder|not_provided": 8,
    "not_provided|Enterokinase_deficiency": 8,
    "not_specified|not_provided|Enterokinase_deficiency": 3,
    "TMPRSS15-related_disorder|Enterokinase_deficiency|not_provided": 1,
    "TMPRSS15-related_disorder": 2,
    "not_provided|TMPRSS15-related_disorder": 3,
    "TMPRSS15-related_disorder|not_specified|not_provided": 1,
    "Enterokinase_deficiency|not_provided|not_specified": 1,
    "NCAM2-related_disorder": 13,
    "Combined_oxidative_phosphorylation_deficiency_59|Leigh_syndrome": 2,
    "Combined_oxidative_phosphorylation_deficiency_59|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Leigh_syndrome|Combined_oxidative_phosphorylation_deficiency_59": 1,
    "Basal_ganglia_calcification|_idiopathic|_8|_autosomal_recessive": 6,
    "Basal_ganglia_calcification|_idiopathic|_8|_autosomal_recessive|not_provided|JAM2-related_disorder": 1,
    "Early-onset_autosomal_dominant_Alzheimer_disease": 2,
    "APP-related_disorder": 16,
    "Alzheimer_disease|not_specified": 12,
    "Alzheimer_disease|APP-related_disorder": 7,
    "Alzheimer_disease|Inborn_genetic_diseases": 5,
    "Alzheimer_disease|not_provided|APP-related_disorder": 1,
    "not_specified|not_provided|Alzheimer_disease": 2,
    "APP-related_disorder|Alzheimer_disease": 6,
    "not_provided|Alzheimer_disease_type_1": 1,
    "Alzheimer_disease_type_1|Alzheimer_disease|not_provided": 1,
    "Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|Alzheimer_disease|not_provided": 1,
    "not_specified|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|APP-related_disorder|Alzheimer_disease|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Alzheimer_disease": 19,
    "APP-related_disorder|not_provided": 2,
    "Alzheimer_disease|Alzheimer_disease_type_1|not_provided": 3,
    "Primary_degenerative_dementia_of_the_Alzheimer_type|_presenile_onset|not_provided|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|Alzheimer_disease": 1,
    "Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease|Hereditary_cerebral_hemorrhage_with_amyloidosis": 1,
    "not_specified|not_provided|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|APP_POLYMORPHISM|Alzheimer_disease": 1,
    "CEREBRAL_AMYLOID_ANGIOPATHY|_APP-RELATED|_PIEDMONT_VARIANT|Cerebral_amyloid_angiopathy|_APP-related|not_provided": 1,
    "ABeta_amyloidosis|_Iowa_type|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease|not_provided": 1,
    "Alzheimer_disease|Alzheimer_disease_type_1|not_provided|ABeta_amyloidosis|_Arctic_type": 1,
    "ABeta_amyloidosis|_dutch_type|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease": 1,
    "ABeta_amyloidosis|_Italian_type|not_provided": 1,
    "Alzheimer_disease_type_1|Alzheimer_disease|not_provided|ABetaA21G_amyloidosis": 1,
    "Alzheimer_disease_type_1|Cerebral_amyloid_angiopathy|_APP-related": 1,
    "Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1": 1,
    "not_specified|Alzheimer_disease": 9,
    "Alzheimer_disease|Alzheimer_disease|_protection_against|not_provided": 1,
    "Alzheimer_disease|Alzheimer_disease_type_1|APP-related_disorder|not_provided": 1,
    "Alzheimer_disease|not_specified|Inborn_genetic_diseases": 1,
    "Alzheimer_disease|APP-related_disorder|Alzheimer_disease_type_1|not_specified|not_provided": 1,
    "Alzheimer_disease|Hereditary_cerebral_hemorrhage_with_amyloidosis": 1,
    "Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|not_specified|Alzheimer_disease": 1,
    "Inborn_genetic_diseases|Alzheimer_disease": 4,
    "not_specified|Alzheimer_disease|not_provided": 3,
    "not_specified|Alzheimer_disease|APP-related_disorder|Vascular_dementia|not_provided": 1,
    "Alzheimer_disease|not_specified|not_provided": 2,
    "Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease": 1,
    "Alzheimer_disease|Inborn_genetic_diseases|Alzheimer_disease_type_1": 1,
    "Alzheimer_disease|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1": 1,
    "Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|Alzheimer_disease": 3,
    "APP-related_disorder|not_specified|not_provided|Alzheimer_disease": 1,
    "Alzheimer_disease|Primary_degenerative_dementia_of_the_Alzheimer_type|_presenile_onset": 1,
    "Alzheimer_disease|Inborn_genetic_diseases|not_specified": 1,
    "APP-related_disorder|Early-onset_autosomal_dominant_Alzheimer_disease|not_provided|Alzheimer_disease|not_specified": 1,
    "not_provided|APP-related_disorder": 1,
    "not_provided|not_specified|Alzheimer_disease": 2,
    "APP-related_disorder|not_specified|Alzheimer_disease": 1,
    "not_specified|Alzheimer_disease|Early-onset_dementia_of_unclear_type": 1,
    "not_provided|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease": 1,
    "Alzheimer_disease|not_provided|not_specified": 2,
    "not_provided|Alzheimer_disease|Inborn_genetic_diseases": 1,
    "not_provided|Alzheimer_disease|not_specified": 1,
    "Alzheimer_disease|Cerebral_amyloid_angiopathy|_APP-related|Alzheimer_disease_type_1|not_provided": 1,
    "Early-onset_autosomal_dominant_Alzheimer_disease|not_provided": 2,
    "Early-onset_autosomal_dominant_Alzheimer_disease|Alzheimer_disease_type_1|Cerebral_amyloid_angiopathy|_APP-related": 1,
    "Cerebral_amyloid_angiopathy|_APP-related|Early-onset_autosomal_dominant_Alzheimer_disease": 1,
    "APP-related_disorder|Alzheimer_disease|not_provided": 1,
    "BACH1-related_disorder": 6,
    "Cerebellar_vermis_hypoplasia": 1,
    "TIAM1-related_disorder": 42,
    "Neurodevelopmental_disorder_with_language_delay_and_seizures": 8,
    "TIAM1-related_disorder|not_provided": 3,
    "not_provided|TIAM1-related_disorder": 5,
    "Neurodevelopmental_disorder_with_language_delay_and_seizures|not_specified": 1,
    "not_specified|TIAM1-related_disorder": 2,
    "not_specified|not_provided|Neurodevelopmental_disorder_with_language_delay_and_seizures": 1,
    "Neurodevelopmental_disorder_with_language_delay_and_seizures|TIAM1-related_disorder|not_provided": 1,
    "Neurodevelopmental_disorder_with_language_delay_and_seizures|not_provided": 2,
    "not_provided|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1": 22,
    "Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_1": 2,
    "Amyotrophic_lateral_sclerosis_type_1|not_provided": 19,
    "SOD1-related_disorder": 9,
    "SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1|SOD1-related_disorder": 3,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1": 4,
    "SOD1-related_disorder|not_provided|Amyotrophic_lateral_sclerosis_type_1": 4,
    "Amyotrophic_lateral_sclerosis_type_1|not_specified": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Spastic_tetraplegia_and_axial_hypotonia|_progressive": 4,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|SOD1-related_disorder": 2,
    "Amyotrophic_lateral_sclerosis_type_1|not_provided|SOD1-related_disorder": 1,
    "Spastic_tetraplegia_and_axial_hypotonia|_progressive|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Motor_neuron_disease|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_10|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|SOD1-related_disorder|Amyotrophic_lateral_sclerosis|not_provided": 1,
    "SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_1": 5,
    "Amyotrophic_lateral_sclerosis_type_1|SOD1-related_disorder|not_provided": 2,
    "SOD1-related_disorder|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "not_specified|SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_1": 1,
    "SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Spastic_tetraplegia_and_axial_hypotonia|_progressive": 1,
    "SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_1|Amyotrophic_lateral_sclerosis_1|_autosomal_recessive|Amyotrophic_lateral_sclerosis|not_specified|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|SOD1-related_disorder": 3,
    "Amyotrophic_lateral_sclerosis_type_1|Motor_neuron_disease": 1,
    "not_provided|Amyotrophic_lateral_sclerosis_type_1|Amyotrophic_lateral_sclerosis_1|_autosomal_recessive": 1,
    "not_provided|SOD1-related_disorder|Amyotrophic_lateral_sclerosis_type_1": 1,
    "not_provided|Amyotrophic_lateral_sclerosis|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Amyotrophic_lateral_sclerosis_type_1|not_provided|Motor_neuron_disease": 1,
    "Abnormal_central_motor_function|Amyotrophic_lateral_sclerosis_1|_autosomal_recessive": 1,
    "Spastic_tetraplegia_and_axial_hypotonia|_progressive|not_provided": 1,
    "SOD1-related_disorder|Motor_neuron_disease|Spastic_tetraplegia_and_axial_hypotonia|_progressive|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Spastic_tetraplegia_and_axial_hypotonia|_progressive|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "Spastic_tetraplegia_and_axial_hypotonia|_progressive": 1,
    "Amyotrophic_lateral_sclerosis_type_1|SOD1-related_disorder|See_cases": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis_type_1|not_specified|not_provided|SOD1-related_disorder": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_1|not_provided": 2,
    "SCAF4-related_disorder": 14,
    "SCAF4-related_disorder|not_provided": 1,
    "Fliedner-Zweier_syndrome": 13,
    "not_provided|Fliedner-Zweier_syndrome": 1,
    "Inborn_genetic_diseases|Fliedner-Zweier_syndrome": 1,
    "Abnormality_of_the_kidney|Multicystic_kidney_dysplasia": 1,
    "Inborn_genetic_diseases|SCAF4-associated_Neurodevelopmental_disorder": 1,
    "SCAF4-related_disorder|Inborn_genetic_diseases": 1,
    "SCAF4-associated_mental_retardation": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder": 2,
    "Fliedner-Zweier_syndrome|Rare_syndromic_intellectual_disability": 1,
    "Glucocorticoid_deficiency_2": 25,
    "Glucocorticoid_deficiency_1|Glucocorticoid_deficiency_2": 1,
    "MRAP-related_disorder": 2,
    "Glucocorticoid_deficiency_2|Glucocorticoid_deficiency_1": 1,
    "not_provided|Glucocorticoid_deficiency_2": 3,
    "Glucocorticoid_deficiency_2|not_provided": 3,
    "MRAP-related_disorder|not_provided": 1,
    "MRAP-related_disorder|Inborn_genetic_diseases": 1,
    "MRAP-related_disorder|Glucocorticoid_deficiency_2": 1,
    "Primary_ciliary_dyskinesia_26|not_provided": 6,
    "Primary_ciliary_dyskinesia_26": 3,
    "CFAP298-related_disorder": 3,
    "not_provided|CFAP298-related_disorder": 2,
    "not_provided|Primary_ciliary_dyskinesia_26": 2,
    "CFAP298-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 586,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 535,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|Inborn_genetic_diseases": 24,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_provided": 21,
    "SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 3,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|not_provided|SYNJ1-related_disorder|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 11,
    "not_provided|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 22,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 12,
    "not_provided|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 7,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_provided": 18,
    "SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Inborn_genetic_diseases|not_provided": 5,
    "SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Inborn_genetic_diseases": 1,
    "SYNJ1-related_disorder": 2,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_specified|not_provided": 1,
    "not_provided|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|Inborn_genetic_diseases": 3,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_provided|SYNJ1-related_disorder": 1,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|Inborn_genetic_diseases|not_provided": 4,
    "SYNJ1-related_disorder|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_provided": 1,
    "not_provided|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 1,
    "not_provided|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|Developmental_and_epileptic_encephalopathy|_1": 2,
    "not_provided|SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 2,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_specified": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Inborn_genetic_diseases|SYNJ1-related_disorder": 1,
    "not_provided|SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|SYNJ1-related_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_53|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_53": 5,
    "Inborn_genetic_diseases|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 1,
    "Early-onset_Parkinson_disease_20": 8,
    "not_provided|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1": 1,
    "SYNJ1-related_disorder|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 1,
    "SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_1": 1,
    "not_specified|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|SYNJ1-related_disorder": 2,
    "not_specified|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|not_provided": 1,
    "SYNJ1-related_disorder|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_provided|not_specified": 1,
    "Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53|Inborn_genetic_diseases|not_provided|SYNJ1-related_disorder": 1,
    "not_specified|not_provided|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 1,
    "SYNJ1-related_disorder|Young-onset_Parkinson_disease|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|SYNJ1-related_disorder|Early-onset_Parkinson_disease_20|Developmental_and_epileptic_encephalopathy|_53": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_53|Early-onset_Parkinson_disease_20": 1,
    "Associated_with_severe_COVID-19_disease|Mortality_risk_in_patients_with_severe_coronavirus_disease_(COVID-19)": 1,
    "Mortality_risk_in_patients_with_severe_coronavirus_disease_(COVID-19)|not_specified|Immunodeficiency_45|not_provided|Hepatitis_B_virus|_susceptibility_to": 1,
    "Mortality_risk_in_patients_with_severe_coronavirus_disease_(COVID-19)|Immunodeficiency_45|not_provided|not_specified": 1,
    "not_specified|Mortality_risk_in_patients_with_severe_coronavirus_disease_(COVID-19)": 1,
    "Immunodeficiency_45": 2,
    "not_provided|Immunodeficiency_45": 2,
    "Primary_immunodeficiency_with_post-measles-mumps-rubella_vaccine_viral_infection|Immunodeficiency_45|not_provided": 2,
    "Immunodeficiency_45|not_provided": 2,
    "not_provided|IFNAR2-related_disorder": 3,
    "Susceptibility_to_severe_COVID-19|not_specified|not_provided": 1,
    "not_provided|Immunodeficiency_45|Hepatitis_B_virus|_susceptibility_to": 1,
    "not_specified|Immunodeficiency_45|Mortality_risk_in_patients_with_severe_coronavirus_disease_(COVID-19)": 1,
    "IFNAR2-related_disorder|not_provided": 4,
    "not_specified|Immunodeficiency_45": 1,
    "IFNAR2-related_disorder": 1,
    "Immunodeficiency_45|not_specified|not_provided": 1,
    "not_provided|not_specified|IFNAR2-related_disorder": 1,
    "Inflammatory_bowel_disease_25": 196,
    "Inflammatory_bowel_disease_25|not_provided": 5,
    "Inborn_genetic_diseases|Inflammatory_bowel_disease_25": 10,
    "IL10RB-related_disorder|Inflammatory_bowel_disease_25": 1,
    "IL10RB-related_disorder|Inflammatory_bowel_disease_25|not_provided": 1,
    "Inflammatory_bowel_disease_25|Inborn_genetic_diseases": 6,
    "not_provided|Inflammatory_bowel_disease_25": 3,
    "Inflammatory_bowel_disease_25|IL10RB-related_disorder": 4,
    "not_provided|Hepatitis_B_virus|_susceptibility_to|Inflammatory_bowel_disease_25|not_specified": 1,
    "Hepatitis_B_virus|_susceptibility_to|Inflammatory_bowel_disease_25": 3,
    "IL10RB-related_disorder|not_provided|Inflammatory_bowel_disease_25": 2,
    "not_provided|Inflammatory_bowel_disease_25|Inborn_genetic_diseases": 1,
    "Inflammatory_bowel_disease_25|Hepatitis_B_virus|_susceptibility_to": 1,
    "Inflammatory_bowel_disease_25|not_provided|Inborn_genetic_diseases": 1,
    "Inflammatory_bowel_disease_25|IL10RB-related_disorder|Hepatitis_B_virus|_susceptibility_to": 1,
    "Inborn_genetic_diseases|Inflammatory_bowel_disease_25|not_provided": 1,
    "Inflammatory_bowel_disease_25|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Inflammatory_bowel_disease_25|not_provided": 1,
    "not_provided|IFNAR1-related_disorder|not_specified": 1,
    "not_provided|Immunodeficiency_106|_susceptibility_to_viral_infections": 2,
    "Immunodeficiency_106|_susceptibility_to_viral_infections": 10,
    "IFNAR1-related_disorder|not_provided": 1,
    "Immunodeficiency_106|_susceptibility_to_viral_infections|not_provided": 1,
    "not_provided|IFNAR1-related_disorder": 1,
    "Immunodeficiency_106|_susceptibility_to_viral_infections|IMMUNODEFICIENCY_106|_SUSCEPTIBILITY_TO_VIRAL_INFECTIONS/IMMUNODEFICIENCY_28|_DIGENIC": 1,
    "Immunodeficiency_28": 168,
    "Inborn_genetic_diseases|IFNGR2-related_disorder|Immunodeficiency_28|not_provided": 1,
    "IFNGR2-related_disorder": 1,
    "Inborn_genetic_diseases|Immunodeficiency_28": 11,
    "not_provided|Immunodeficiency_28|not_specified": 1,
    "not_provided|Immunodeficiency_28": 12,
    "Interferon_gamma_receptor_deficiency|Immunodeficiency_28|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency_28": 2,
    "Immunodeficiency_28|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|not_specified|Immunodeficiency_28": 1,
    "IFNGR2-related_disorder|Immunodeficiency_28": 1,
    "Immunodeficiency_28|not_provided|Immunodeficiency_27A": 1,
    "Immunodeficiency_28|not_specified|not_provided": 2,
    "Immunodeficiency_28|Immunodeficiency_27A": 1,
    "Inborn_genetic_diseases|Immunodeficiency_28|not_provided": 1,
    "Immunodeficiency_28|not_provided": 2,
    "not_specified|not_provided|IFNGR2-related_disorder|Immunodeficiency_28": 1,
    "IFNGR2-related_disorder|Immunodeficiency_28|not_provided": 1,
    "not_provided|Interferon_gamma_receptor_deficiency|Immunodeficiency_28": 1,
    "Immunodeficiency_28|not_specified": 1,
    "not_provided|IFNGR2-related_disorder|Immunodeficiency_28": 1,
    "not_provided|SON-related_disorder": 32,
    "ZTTK_syndrome|not_provided": 29,
    "SON-related_disorder": 26,
    "ZTTK_syndrome|Failure_to_thrive|Global_developmental_delay": 3,
    "not_provided|Inborn_genetic_diseases|ZTTK_syndrome": 1,
    "SON-related_disorder|not_specified|not_provided": 2,
    "not_provided|ZTTK_syndrome": 24,
    "Inborn_genetic_diseases|not_provided|SON-related_disorder": 2,
    "SON-related_disorder|not_provided": 25,
    "SON-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "ZTTK_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|SON-related_disorder|Inborn_genetic_diseases": 2,
    "SON-related_disorder|not_specified": 1,
    "ZTTK_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|SON-related_disorder": 1,
    "ZTTK_syndrome|Inborn_genetic_diseases": 1,
    "SON-related_disorder|ZTTK_syndrome|not_provided": 1,
    "not_provided|SON-related_disorder|ZTTK_syndrome": 1,
    "Failure_to_thrive|Global_developmental_delay|ZTTK_syndrome|not_provided": 1,
    "not_specified|SON-related_disorder|not_provided": 1,
    "SON-related_disorder|not_provided|Intellectual_disability": 1,
    "ZTTK_syndrome|SON-related_disorder|not_provided": 2,
    "SON-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "SON-related_disorder|ZTTK_syndrome": 3,
    "SON-related_disorder|Intellectual_disability|not_provided": 1,
    "Inborn_genetic_diseases|ZTTK_syndrome": 1,
    "See_cases|ZTTK_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|ZTTK_syndrome": 1,
    "not_provided|Hereditary_spastic_paraplegia_17|Neurodevelopmental_abnormality|Global_developmental_delay|Failure_to_thrive|See_cases|ZTTK_syndrome|Inborn_genetic_diseases": 1,
    "SON-related_disorder|not_specified|ZTTK_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "SON-related_disorder|not_provided|not_specified": 1,
    "DONSON-related_disorder": 3,
    "not_provided|DONSON-related_disorder": 3,
    "DONSON-related_disorder|not_provided": 7,
    "Microcephaly-micromelia_syndrome|Microcephaly|_short_stature|_and_limb_abnormalities": 1,
    "DONSON-related_disorder|Microcephaly-micromelia_syndrome|Microcephaly|_short_stature|_and_limb_abnormalities|Inborn_genetic_diseases|not_specified|not_provided|Microcephaly|See_cases": 1,
    "Microcephaly|_short_stature|_and_limb_abnormalities": 9,
    "Microcephaly-micromelia_syndrome|Microcephaly|_short_stature|_and_limb_abnormalities|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Microcephaly|_short_stature|_and_limb_abnormalities|Inborn_genetic_diseases": 1,
    "Microcephaly|_short_stature|_and_limb_abnormalities|Inborn_genetic_diseases": 1,
    "not_provided|DONSON-related_disorder|Microcephaly|_short_stature|_and_limb_abnormalities|Microcephaly-micromelia_syndrome": 1,
    "not_provided|Microcephaly|_short_stature|_and_limb_abnormalities": 1,
    "DONSON-related_Meier-Gorlin_syndrome|Meier-Gorlin_syndrome|not_provided": 1,
    "Microcephaly|_short_stature|_and_limb_abnormalities|Microcephaly-micromelia_syndrome": 2,
    "Microcephaly|_short_stature|_and_limb_abnormalities|Meier-Gorlin_syndrome|not_provided|DONSON-related_Meier-Gorlin_syndrome": 1,
    "Microcephaly|_short_stature|_and_limb_abnormalities|Meier-Gorlin_syndrome": 1,
    "Microcephaly-micromelia_syndrome|Microcephaly|_short_stature|_and_limb_abnormalities|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|ITSN1-related_disorder": 2,
    "ITSN1-related_disorder": 44,
    "ITSN1-related_disorder|not_provided": 6,
    "ITSN1-related_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|ITSN1-related_disorder": 3,
    "ITSN1-related_neurodevelopmental_disorders": 1,
    "Autistic_behavior|not_provided": 1,
    "Generalized-onset_seizure": 1,
    "not_provided|Esophageal_atresia/tracheoesophageal_fistula": 1,
    "not_specified|ITSN1-related_disorder|not_provided": 1,
    "ATP5PO-related_disorder|not_specified": 1,
    "Severe_global_developmental_delay|Dysphagia|Seizure|Microcephaly|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_7": 2,
    "Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_7|ATP5PO-related_disorder|Leigh_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|Familial_atrial_fibrillation": 1,
    "Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6|not_provided": 1,
    "Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6": 2,
    "Atrial_fibrillation|_familial|_4|Congenital_long_QT_syndrome|Long_QT_syndrome_6|not_provided": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|not_provided": 1,
    "not_provided|Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4": 5,
    "Long_QT_syndrome_6|not_specified|Atrial_fibrillation|_familial|_4": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6": 3,
    "Cardiovascular_phenotype|Long_QT_syndrome|_drug-associated|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_6": 1,
    "Long_QT_syndrome_6|_acquired|_susceptibility_to|Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Long_QT_syndrome_6": 32,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Long_QT_syndrome|Hypertrophic_cardiomyopathy|Long_QT_syndrome_6|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_6": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_6|not_specified": 3,
    "not_provided|Cardiovascular_phenotype|Long_QT_syndrome_6|Long_QT_syndrome": 1,
    "Long_QT_syndrome_6|Cardiovascular_phenotype|not_provided": 2,
    "Long_QT_syndrome_6|not_provided": 1,
    "Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_6": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_6": 9,
    "Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Long_QT_syndrome_6": 2,
    "Cardiovascular_phenotype|Primary_familial_hypertrophic_cardiomyopathy|Long_QT_syndrome|Atrial_fibrillation|Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|not_provided": 1,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_6|Long_QT_syndrome|Atrial_fibrillation|_familial|_4|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome_6|Cardiovascular_phenotype": 9,
    "Cardiovascular_phenotype|Long_QT_syndrome_6|not_provided": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4": 1,
    "Long_QT_syndrome_6|not_provided|Cardiovascular_phenotype": 1,
    "KCNE2-related_disorder|Long_QT_syndrome_6|Congenital_long_QT_syndrome|not_specified|Long_QT_syndrome|not_provided|Cardiovascular_phenotype|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|not_provided|Cardiovascular_phenotype|KCNE2-related_disorder|Cardiac_arrhythmia": 1,
    "Long_QT_syndrome_3/6|_digenic|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_6|Congenital_long_QT_syndrome": 1,
    "Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome_6": 2,
    "Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|Cardiovascular_phenotype": 1,
    "not_provided|Long_QT_syndrome_6|Cardiovascular_phenotype": 3,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_6|Long_QT_syndrome|Atrial_fibrillation|_familial|_4|not_specified|not_provided": 1,
    "Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6|Cardiovascular_phenotype": 2,
    "not_specified|Long_QT_syndrome_6|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome_6|Congenital_long_QT_syndrome": 1,
    "not_provided|Long_QT_syndrome_6|Acquired_long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Atrial_fibrillation|_familial|_4|Long_QT_syndrome_6|not_specified|not_provided": 1,
    "Long_QT_syndrome_6|Atrial_fibrillation|_familial|_4|Cardiovascular_phenotype|not_provided": 1,
    "Congenital_long_QT_syndrome|Atrial_fibrillation|_familial|_4|not_provided|Long_QT_syndrome_6": 1,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2|not_provided|Long_QT_syndrome_5": 4,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|not_provided": 4,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5": 5,
    "Jervell_and_Lange-Nielsen_syndrome_2|Congenital_long_QT_syndrome|Long_QT_syndrome_5": 5,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 15,
    "Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 14,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5": 10,
    "not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "Congenital_long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|not_provided": 1,
    "Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Congenital_long_QT_syndrome": 3,
    "Long_QT_syndrome_5|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2": 6,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome": 2,
    "not_provided|Congenital_long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome": 3,
    "Jervell_and_Lange-Nielsen_syndrome_2|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_5": 1,
    "Congenital_long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5": 2,
    "Long_QT_syndrome_5|Congenital_long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome_2": 2,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Long_QT_syndrome_5": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 1,
    "KCNE1-related_disorder": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome|Long_QT_syndrome_5": 1,
    "Long_QT_syndrome|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Long_QT_syndrome_2/5|_digenic|Long_QT_syndrome|not_provided|Long_QT_syndrome_5|_acquired|_susceptibility_to|Cardiomyopathy|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 2,
    "Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome|Congenital_long_QT_syndrome|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_1": 1,
    "KCNE1-related_disorder|Cardiovascular_phenotype|not_provided|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|not_specified|Long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "not_specified|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5": 1,
    "Congenital_long_QT_syndrome|Cardiovascular_phenotype|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_5": 1,
    "Cardiovascular_phenotype|not_specified|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_5": 1,
    "Cardiovascular_phenotype|not_provided|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 2,
    "Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|not_provided|Long_QT_syndrome": 1,
    "not_specified|not_provided|Long_QT_syndrome|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|not_specified|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Long_QT_syndrome|not_specified|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|not_provided": 1,
    "Cardiomyopathy|not_specified|Long_QT_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "not_provided|Rare_genetic_deafness|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Long_QT_syndrome_5|not_provided": 1,
    "KCNE1-related_disorder|Long_QT_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Congenital_long_QT_syndrome|Noise_induced_hearing_loss|not_provided|not_specified|Long_QT_syndrome_5|Long_QT_syndrome|Cardiovascular_phenotype|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|not_provided|Long_QT_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|not_provided": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Cardiovascular_phenotype|Long_QT_syndrome|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Long_QT_syndrome|Long_QT_syndrome_5": 1,
    "Long_QT_syndrome|Hereditary_hearing_loss_and_deafness": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 1,
    "Long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Congenital_long_QT_syndrome|Long_QT_syndrome": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome|Sensorineural_hearing_loss_disorder": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "KCNE1-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|not_provided|Long_QT_syndrome|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "KCNE1-related_disorder|Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_provided|not_specified|Long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "KCNE1-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|Congenital_long_QT_syndrome|not_specified|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Long_QT_syndrome": 1,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|Cardiovascular_phenotype|Long_QT_syndrome": 1,
    "Cardiovascular_phenotype|not_specified|Long_QT_syndrome|not_provided|KCNE1-related_disorder": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Congenital_long_QT_syndrome|Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|not_specified": 2,
    "Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2|not_provided": 1,
    "Jervell_and_Lange-Nielsen_syndrome_2|Long_QT_syndrome_5|Congenital_long_QT_syndrome|not_provided": 3,
    "Congenital_long_QT_syndrome|not_provided|Long_QT_syndrome_5|Jervell_and_Lange-Nielsen_syndrome_2": 1,
    "Jervell_and_Lange-Nielsen_syndrome|Long_QT_syndrome|Congenital_long_QT_syndrome": 2,
    "not_provided|Jervell_and_Lange-Nielsen_syndrome|Long_QT_syndrome|Congenital_long_QT_syndrome": 1,
    "RCAN1-related_disorder": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 403,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 383,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 6,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 3,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 35,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 11,
    "not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 10,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia": 3,
    "not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 1,
    "not_provided|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 8,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 35,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 39,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 45,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 64,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 55,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 6,
    "not_specified|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 19,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 39,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 9,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 41,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 5,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_specified|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|RUNX1-related_disorder|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 42,
    "not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 7,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 2,
    "not_specified|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 3,
    "not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 25,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 2,
    "Inborn_genetic_diseases|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 1,
    "RUNX1-related_disorder|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Acute_myeloid_leukemia": 3,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Aggressive_systemic_mastocytosis|Abnormal_bleeding|Thrombocytopenia": 1,
    "Thrombocytopenia|Abnormal_bleeding|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "not_specified|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 2,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 5,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Abnormal_bleeding|Thrombocytopenia": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 4,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|RUNX1-related_disorder": 1,
    "Atypical_chronic_myeloid_leukemia|_BCR-ABL1_negative|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|not_specified|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Thrombocytopenia|Abnormal_bleeding|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|Aggressive_systemic_mastocytosis": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|not_provided|RUNX1-related_disorder|Acute_myeloid_leukemia": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 2,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 34,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_specified|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 3,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 2,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Acute_myeloid_leukemia": 2,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 1,
    "Thrombocytopenia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 6,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 2,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_specified": 2,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 5,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 2,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 7,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Myelodysplasia": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 2,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|RUNX1-related_disorder|not_specified|Acute_myeloid_leukemia": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 2,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 6,
    "not_provided|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|RUNX1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 4,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 2,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 4,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 4,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Thrombocytopenia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|RUNX1-related_disorder": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|not_provided": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 4,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Thrombocytopenia": 2,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Inborn_genetic_diseases": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 3,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|Inborn_genetic_diseases": 1,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 1,
    "Storage_pool_disease_of_platelets|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 2,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 6,
    "Acute_myeloid_leukemia|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 4,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|RUNX1-related_disorder|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified|Acute_myeloid_leukemia": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified|not_provided": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Abnormal_bleeding|Thrombocytopenia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Thrombocytopenia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 2,
    "not_provided|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Thrombocytopenia": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Abnormal_bleeding|Thrombocytopenia": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia": 2,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Abnormal_bleeding|Thrombocytopenia": 3,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Thrombocytopenia": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Clonal_Cytopenia_of_Undetermined_Significance|Pancytopenia": 1,
    "RUNX1-related_disorder|not_provided|Inborn_genetic_diseases|Inherited_bleeding_disorder|_platelet-type|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Abnormal_platelet_function": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia|Inborn_genetic_diseases": 2,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Thrombocytopenia": 1,
    "RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_specified|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Castleman-Kojima_disease|RUNX1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|TRANSIENT_MYELOPROLIFERATIVE_DISORDER_OF_DOWN_SYNDROME|LEUKEMIA|_ACUTE_MYELOID|_M0_SUBTYPE": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia": 1,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder": 1,
    "not_specified|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Acute_myeloid_leukemia": 1,
    "not_specified|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|RUNX1-related_disorder|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "RUNX1-related_disorder|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases|not_provided|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Anaplastic_ependymoma|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|RUNX1-related_disorder|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified|not_provided": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified": 1,
    "Thrombocytopenia|Abnormal_bleeding|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided|Acute_myeloid_leukemia|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_specified": 1,
    "Inborn_genetic_diseases|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|not_specified|Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Inborn_genetic_diseases|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|RUNX1-related_disorder": 1,
    "Acute_myeloid_leukemia|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_thrombocytopenia_and_hematological_cancer_predisposition_syndrome_associated_with_RUNX1|Hereditary_thrombocytopenia_and_hematologic_cancer_predisposition_syndrome|Acute_myeloid_leukemia|not_provided": 1,
    "Global_developmental_delay|Attention_deficit_hyperactivity_disorder|Intellectual_disability": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29": 37,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_29": 16,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|not_provided|CLDN14-related_disorder|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|not_specified|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_29|not_specified": 1,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_29": 2,
    "not_provided|CLDN14-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_29": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|not_provided": 3,
    "not_specified|Monogenic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_29": 1,
    "Vein_of_Galen_aneurysmal_malformation|not_provided": 1,
    "CLDN14-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|not_provided|not_specified": 1,
    "Hearing_impairment|Autosomal_recessive_nonsyndromic_hearing_loss_29|not_provided": 1,
    "CLDN14-related_disorder|not_specified": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_29|not_provided": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|Hearing_loss|_autosomal_recessive|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|CLDN14-related_disorder|Hearing_impairment|not_provided": 1,
    "not_provided|Vein_of_Galen_aneurysmal_malformation|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_29|CLDN14-related_disorder": 1,
    "Neurodevelopmental_with_craniofacial_anomalies_disorder": 1,
    "Holocarboxylase_synthetase_deficiency": 792,
    "not_provided|Holocarboxylase_synthetase_deficiency": 24,
    "Holocarboxylase_synthetase_deficiency|not_provided": 19,
    "Holocarboxylase_synthetase_deficiency|not_provided|not_specified": 3,
    "not_specified|Holocarboxylase_synthetase_deficiency|not_provided": 3,
    "not_provided|not_specified|Holocarboxylase_synthetase_deficiency": 5,
    "Holocarboxylase_synthetase_deficiency|Inborn_genetic_diseases": 21,
    "not_specified|Holocarboxylase_synthetase_deficiency": 18,
    "Holocarboxylase_synthetase_deficiency|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Holocarboxylase_synthetase_deficiency": 15,
    "Holocarboxylase_synthetase_deficiency|not_specified": 13,
    "Inborn_genetic_diseases|Holocarboxylase_synthetase_deficiency|not_provided": 1,
    "Holocarboxylase_synthetase_deficiency|not_provided|Inborn_genetic_diseases": 3,
    "not_provided|Holocarboxylase_synthetase_deficiency|not_specified": 6,
    "Holocarboxylase_synthetase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "HLCS-related_disorder|Holocarboxylase_synthetase_deficiency|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Holocarboxylase_synthetase_deficiency": 1,
    "HLCS-related_disorder|Holocarboxylase_synthetase_deficiency": 1,
    "not_provided|Holocarboxylase_synthetase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Holocarboxylase_synthetase_deficiency|HLCS-related_disorder": 1,
    "not_specified|not_provided|Holocarboxylase_synthetase_deficiency": 3,
    "Inborn_genetic_diseases|not_provided|Holocarboxylase_synthetase_deficiency": 2,
    "not_specified|Holocarboxylase_synthetase_deficiency|Inborn_genetic_diseases": 1,
    "Holocarboxylase_synthetase_deficiency|HLCS-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Holocarboxylase_synthetase_deficiency|HLCS-related_disorder|not_provided|not_specified": 1,
    "Holocarboxylase_synthetase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "Holocarboxylase_synthetase_deficiency|HLCS-related_disorder|not_specified": 1,
    "HLCS-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|Developmental_and_epileptic_encephalopathy|_55": 1,
    "not_provided|PIGP-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_55": 1,
    "PIGP-related_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_55|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|not_provided|See_cases|PIGP-related_disorder|Developmental_and_epileptic_encephalopathy|_55": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_55|Inborn_genetic_diseases": 1,
    "PIGP-related_disorder": 1,
    "Corticobasal_syndrome": 1,
    "VPS26C-related_disorder": 1,
    "DYRK1A-related_intellectual_disability_syndrome": 580,
    "DYRK1A-related_intellectual_disability_syndrome|not_specified": 18,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome": 42,
    "Inborn_genetic_diseases|DYRK1A-related_intellectual_disability_syndrome": 18,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided": 43,
    "DYRK1A-related_intellectual_disability_syndrome|Inborn_genetic_diseases": 18,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|not_specified": 2,
    "not_specified|DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|DYRK1A-related_intellectual_disability_syndrome": 4,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome|Intellectual_disability": 1,
    "not_specified|DYRK1A-related_intellectual_disability_syndrome": 10,
    "not_provided|Intellectual_disability|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|DYRK1A-related_intellectual_disability_syndrome": 1,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome|Inborn_genetic_diseases": 7,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|DYRK1A-related_disorder|Inborn_genetic_diseases": 3,
    "not_specified|DYRK1A-related_intellectual_disability_syndrome|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|DYRK1A-related_intellectual_disability_syndrome": 2,
    "Complex_neurodevelopmental_disorder|DYRK1A-related_intellectual_disability_syndrome": 1,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome|not_specified": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|DYRK1A-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Complex_neurodevelopmental_disorder|not_provided|DYRK1A-related_intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|Global_developmental_delay|Generalized-onset_seizure|Microcephaly|Microphthalmia|not_provided|DYRK1A-related_intellectual_disability_syndrome|Intellectual_disability|Deeply_set_eye|Feeding_difficulties|Absent_or_delayed_speech_development": 1,
    "Intellectual_disability|Microcephaly|Absent_or_delayed_speech_development|Deeply_set_eye|Feeding_difficulties": 1,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome|Complex_neurodevelopmental_disorder": 1,
    "not_provided|Intellectual_disability|See_cases|DYRK1A-related_intellectual_disability_syndrome": 1,
    "DYRK1A-related_intellectual_disability_syndrome|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|Complex_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|DYRK1A-related_intellectual_disability_syndrome|Autism_spectrum_disorder|Intellectual_disability|Absent_or_delayed_speech_development|Microcephaly|Deeply_set_eye|Seizure|Feeding_difficulties": 1,
    "not_provided|Global_developmental_delay|DYRK1A-related_intellectual_disability_syndrome": 1,
    "DYRK1A-related_disorder|DYRK1A-related_intellectual_disability_syndrome": 2,
    "DYRK1A-related_intellectual_disability_syndrome|Inborn_genetic_diseases|not_specified": 3,
    "Microcephaly|Absent_or_delayed_speech_development|Intellectual_disability|Deeply_set_eye|Seizure|Feeding_difficulties": 4,
    "not_specified|DYRK1A-related_intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Intellectual_disability|DYRK1A-related_intellectual_disability_syndrome": 1,
    "not_provided|Complex_neurodevelopmental_disorder|DYRK1A-related_intellectual_disability_syndrome": 1,
    "Intellectual_disability|DYRK1A-related_intellectual_disability_syndrome": 2,
    "DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder": 3,
    "not_provided|not_specified|DYRK1A-related_intellectual_disability_syndrome": 1,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "DYRK1A-related_intellectual_disability_syndrome|Intellectual_disability|See_cases": 1,
    "Inborn_genetic_diseases|not_specified|DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder|not_provided": 1,
    "DYRK1A-related_disorder": 3,
    "DYRK1A-related_disorder|DYRK1A-related_intellectual_disability_syndrome|not_provided": 1,
    "Complex_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|DYRK1A-related_intellectual_disability_syndrome|Intellectual_disability|Seizure|Feeding_difficulties|Absent_or_delayed_speech_development|Deeply_set_eye|Microcephaly": 1,
    "DYRK1A-related_disorder|DYRK1A-related_intellectual_disability_syndrome|not_specified": 1,
    "not_provided|DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder": 1,
    "DYRK1A-related_intellectual_disability_syndrome|Complex_neurodevelopmental_disorder|Intellectual_disability|not_provided": 1,
    "DYRK1A-related_intellectual_disability_syndrome|Complex_neurodevelopmental_disorder": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "Intellectual_disability_syndrome_due_to_a_DYRK1A_point_mutation": 1,
    "not_specified|not_provided|DYRK1A-related_intellectual_disability_syndrome": 2,
    "DYRK1A-related_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|DYRK1A-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|DYRK1A-related_disorder|DYRK1A-related_intellectual_disability_syndrome": 1,
    "Microcephaly|Absent_or_delayed_speech_development|Intellectual_disability|Deeply_set_eye|Seizure|DYRK1A-related_intellectual_disability_syndrome": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder|Inborn_genetic_diseases": 1,
    "DYRK1A-related_intellectual_disability_syndrome|Inborn_genetic_diseases|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|DYRK1A-related_intellectual_disability_syndrome": 1,
    "not_specified|DYRK1A-related_intellectual_disability_syndrome|Intellectual_disability|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|DYRK1A-related_intellectual_disability_syndrome|DYRK1A-related_disorder": 1,
    "DYRK1A-related_intellectual_disability_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|DYRK1A-related_disorder|DYRK1A-related_intellectual_disability_syndrome": 1,
    "Keppen-Lubinsky_syndrome|not_provided": 2,
    "Keppen-Lubinsky_syndrome": 9,
    "KCNJ6-related_disorder": 2,
    "Keppen-Lubinsky_syndrome|See_cases": 1,
    "not_provided|KCNJ6-related_disorder|Inborn_genetic_diseases": 1,
    "Lymphatic_malformation_14": 3,
    "BRWD1-related_disorder": 37,
    "BRWD1-related_disorder|not_specified|not_provided": 1,
    "Bronchiectasis|Male_infertility|Situs_inversus|Recurrent_otitis_media|Recurrent_sinusitis|Ciliary_dyskinesia|_primary|_51": 2,
    "not_specified|BRWD1-related_disorder": 1,
    "BRWD1-related_disorder|not_specified": 1,
    "Ciliary_dyskinesia|_primary|_51": 2,
    "not_provided|BRWD1-related_disorder": 1,
    "Bronchiectasis|Male_infertility|Situs_inversus|Recurrent_sinusitis": 1,
    "Bronchiectasis|Male_infertility|Situs_inversus|Recurrent_otitis_media|Recurrent_sinusitis": 1,
    "DSCAM-related_disorder": 26,
    "not_provided|DSCAM-related_disorder": 6,
    "DSCAM-related_disorder|not_provided": 3,
    "DSCAM-related_disorder|Autism": 1,
    "BACE2-related_disorder": 4,
    "BACE2-related_disorder|not_provided": 3,
    "PLAC4-related_disorder": 1,
    "not_provided|BACE2-related_disorder": 1,
    "not_provided|TMPRSS2-related_disorder": 1,
    "TMPRSS2-related_disorder": 2,
    "Bartsocas-Papas_syndrome_1": 68,
    "Bartsocas-Papas_syndrome_1|not_provided": 13,
    "not_provided|Bartsocas-Papas_syndrome_1": 18,
    "Inborn_genetic_diseases|RIPK4-related_disorder": 1,
    "not_specified|not_provided|Bartsocas-Papas_syndrome_1": 5,
    "Inborn_genetic_diseases|RIPK4-related_disorder|not_provided": 1,
    "RIPK4-related_disorder|not_provided|Bartsocas-Papas_syndrome_1": 7,
    "Inborn_genetic_diseases|Bartsocas-Papas_syndrome_1|not_provided|RIPK4-related_disorder": 1,
    "RIPK4-related_disorder": 12,
    "RIPK4-related_disorder|Bartsocas-Papas_syndrome_1": 1,
    "RIPK4-related_disorder|not_provided": 2,
    "not_specified|Bartsocas-Papas_syndrome_1|not_provided": 2,
    "Bartsocas-Papas_syndrome_1|RIPK4-related_disorder|not_specified|not_provided": 1,
    "Bartsocas-Papas_syndrome_1|Inborn_genetic_diseases": 4,
    "Bartsocas-Papas_syndrome_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Bartsocas-Papas_syndrome_1": 4,
    "RIPK4-related_disorder|Bartsocas-Papas_syndrome_1|not_provided": 1,
    "RIPK4-related_disorder|Inborn_genetic_diseases|not_provided|Bartsocas-Papas_syndrome_1": 1,
    "Inborn_genetic_diseases|not_provided|Bartsocas-Papas_syndrome_1": 1,
    "Curly_hair|_ankyloblepharon|_nail_dysplasia_syndrome": 1,
    "Bartsocas-Papas_syndrome_1|Curly_hair|_ankyloblepharon|_nail_dysplasia_syndrome": 1,
    "Bartsocas-Papas_syndrome_1|Curly_hair|_ankyloblepharon|_nail_dysplasia_syndrome|not_provided": 1,
    "not_provided|Pervasive_developmental_disorder": 1,
    "ABCG1-related_disorder": 22,
    "not_provided|ABCG1-related_disorder": 2,
    "ABCG1-related_disorder|not_provided": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 19,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|not_provided": 24,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|not_specified": 12,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|not_specified|not_provided": 3,
    "not_provided|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_8": 2,
    "TMPRSS3-related_disorder|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|not_specified|not_provided|TMPRSS3-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|Rare_genetic_deafness|not_provided": 1,
    "Rare_genetic_deafness|TMPRSS3-related_disorder|not_provided|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "TMPRSS3-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_loss|_autosomal_recessive": 2,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|Ear_malformation": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|not_specified": 2,
    "Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|Rare_genetic_deafness": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 3,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|TMPRSS3-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Hearing_impairment": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_8|not_provided": 3,
    "TMPRSS3-related_disorder|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|not_provided|not_specified": 5,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_impairment": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_loss|_autosomal_recessive": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_impairment": 1,
    "TMPRSS3-related_disorder|Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "TMPRSS3-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 2,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 2,
    "not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_8|not_specified": 1,
    "not_provided|Hearing_impairment|Rare_genetic_deafness|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_impairment|not_provided": 1,
    "TMPRSS3-related_disorder|not_specified": 1,
    "Rare_genetic_deafness|not_provided|TMPRSS3-related_disorder|Hearing_impairment|Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|Waardenburg_syndrome|not_provided|not_specified": 1,
    "not_provided|TMPRSS3-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|TMPRSS3-related_disorder": 1,
    "Rare_genetic_deafness|TMPRSS3-related_disorder|Childhood_onset_hearing_loss|not_provided|Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_impairment": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|TMPRSS3-related_disorder|Hearing_impairment": 1,
    "not_specified|not_provided|TMPRSS3-related_disorder": 1,
    "TMPRSS3-related_disorder|Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "Inborn_genetic_diseases|TMPRSS3-related_disorder|Rare_genetic_deafness|Nonsyndromic_genetic_hearing_loss|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8|Hearing_impairment": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_8|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_8": 1,
    "UBASH3A-related_disorder": 1,
    "Primary_ciliary_dyskinesia_24|Primary_ciliary_dyskinesia": 6,
    "RSPH1-related_disorder|Primary_ciliary_dyskinesia_24|Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_24": 3,
    "Primary_ciliary_dyskinesia|RSPH1-related_disorder": 5,
    "not_provided|Primary_ciliary_dyskinesia|Primary_ciliary_dyskinesia_24|not_specified": 2,
    "not_provided|Primary_ciliary_dyskinesia_24": 1,
    "Primary_ciliary_dyskinesia|not_provided|Primary_ciliary_dyskinesia_24": 1,
    "Primary_ciliary_dyskinesia_24|not_provided|Primary_ciliary_dyskinesia": 2,
    "RSPH1-related_disorder": 1,
    "Primary_ciliary_dyskinesia_24|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia_24|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_24": 2,
    "RSPH1-related_disorder|Inborn_genetic_diseases|Primary_ciliary_dyskinesia": 1,
    "not_provided|Inborn_genetic_diseases|Primary_ciliary_dyskinesia|RSPH1-related_disorder": 1,
    "Primary_ciliary_dyskinesia_24|Kartagener_syndrome": 1,
    "RSPH1-related_disorder|Primary_ciliary_dyskinesia_24": 1,
    "RSPH1-related_disorder|Primary_ciliary_dyskinesia_24|Primary_ciliary_dyskinesia": 1,
    "RSPH1-related_disorder|Primary_ciliary_dyskinesia_24|not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "Primary_ciliary_dyskinesia_24|not_provided|Primary_ciliary_dyskinesia|Kartagener_syndrome": 1,
    "RSPH1-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia_24|not_provided": 1,
    "not_provided|Galloway-Mowat_syndrome_6|Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations": 3,
    "Inborn_genetic_diseases|not_provided|WDR4-related_disorder": 1,
    "WDR4-related_disorder|not_provided": 5,
    "WDR4-related_disorder": 5,
    "Inborn_genetic_diseases|WDR4-related_disorder": 1,
    "not_provided|Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations|Galloway-Mowat_syndrome_6": 4,
    "not_provided|WDR4-related_disorder": 12,
    "Galloway-Mowat_syndrome_6": 6,
    "Galloway-Mowat_syndrome_6|not_provided": 1,
    "Inborn_genetic_diseases|WDR4-related_disorder|not_provided": 2,
    "Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations|Inborn_genetic_diseases": 1,
    "not_provided|WDR4-related_disorder|Inborn_genetic_diseases": 2,
    "Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations|Galloway-Mowat_syndrome_6": 1,
    "not_provided|Galloway-Mowat_syndrome_6": 2,
    "Galloway-Mowat_syndrome_6|Galloway-Mowat_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations|Galloway-Mowat_syndrome_6": 1,
    "Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations": 1,
    "Microcephaly|_growth_deficiency|_seizures|_and_brain_malformations": 1,
    "NDUFV3-related_disorder": 14,
    "NDUFV3-related_disorder|not_provided": 1,
    "NDUFV3-related_disorder|not_provided|not_specified": 1,
    "Classic_homocystinuria|not_provided": 2,
    "not_provided|Classic_homocystinuria": 14,
    "not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified": 1,
    "Homocystinuria": 9,
    "not_specified|Classic_homocystinuria": 2,
    "not_specified|not_provided|Classic_homocystinuria": 2,
    "not_specified|CBS-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria": 6,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 41,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 529,
    "CBS-related_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "CBS-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 2,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|not_provided": 1,
    "not_specified|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 3,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Homocystinuria|Classic_homocystinuria|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 2,
    "CBS-related_disorder|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 12,
    "Classic_homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 34,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 39,
    "not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 10,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 6,
    "Homocystinuria|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 10,
    "not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria": 25,
    "not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 18,
    "not_specified|Connective_tissue_disorder|CBS-related_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided": 12,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided": 9,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|Classic_homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|not_provided": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Classic_homocystinuria": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria": 1,
    "not_provided|not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 3,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified": 11,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 5,
    "Cardiovascular_phenotype|Classic_homocystinuria": 1,
    "Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_specified|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 3,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 4,
    "CBS-related_disorder|not_specified|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|not_specified|not_provided": 1,
    "not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 11,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 2,
    "not_provided|not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "CBS-related_disorder|Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|_pyridoxine-responsive": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 5,
    "Classic_homocystinuria|CBS-related_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 3,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|CBS-related_disorder|not_provided": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "CBS-related_disorder|Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "CBS-related_disorder": 7,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|not_provided": 1,
    "not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided": 1,
    "Classic_homocystinuria|Homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Classic_homocystinuria": 5,
    "Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Homocystinuria": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided": 2,
    "Classic_homocystinuria|Homocystinuria|not_provided": 1,
    "Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "CBS-related_disorder|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Homocystinuria|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 7,
    "CBS-related_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria": 1,
    "CBS-related_disorder|Homocystinuria|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|not_provided": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|not_provided|Classic_homocystinuria": 2,
    "CBS-related_disorder|Connective_tissue_disorder|Cardiovascular_phenotype|Congenital_myopathy|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 3,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 1,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|_pyridoxine-nonresponsive": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Homocystinuria|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 3,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|not_provided": 4,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Classic_homocystinuria": 1,
    "Cardiovascular_phenotype|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|Homocystinuria": 3,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Homocystinuria|not_provided|Classic_homocystinuria": 1,
    "not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Intellectual_disability": 1,
    "Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 2,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|not_provided|CBS-related_disorder|Classic_homocystinuria": 1,
    "Cardiovascular_phenotype|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|not_specified|Homocystinuria": 1,
    "not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified": 1,
    "not_specified|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Classic_homocystinuria": 1,
    "CBS-related_disorder|Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|_pyridoxine-nonresponsive": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Classic_homocystinuria|Homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|not_specified": 1,
    "not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 2,
    "not_provided|Homocystinuria|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|Homocystinuria": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 2,
    "not_specified|Intellectual_disability|Congenital_myopathy|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS_POLYMORPHISM|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Connective_tissue_disorder|Thoracic_aortic_aneurysm_or_dissection|Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|See_cases|Intellectual_disability": 1,
    "not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Classic_homocystinuria": 1,
    "CBS-related_disorder|not_specified|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria": 2,
    "Homocystinuria|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Homocystinuria|not_provided|Hyperhomocysteinemia|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|See_cases": 1,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder": 1,
    "not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|Classic_homocystinuria": 1,
    "Connective_tissue_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Homocystinuria|Classic_homocystinuria": 2,
    "Homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria": 1,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|Homocystinuria|not_provided": 1,
    "CBS-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Intellectual_disability|not_provided|Classic_homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|CBS-related_disorder|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|not_specified": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 2,
    "CBS-related_disorder|Homocystinuria|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|_pyridoxine-nonresponsive": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder": 1,
    "Homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Classic_homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Homocystinuria|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|_pyridoxine-responsive": 1,
    "Classic_homocystinuria|Homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|See_cases": 1,
    "CBS-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|not_provided": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria": 1,
    "Homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|CBS-related_disorder": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Classic_homocystinuria|Homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|CBS-related_disorder|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria|not_specified": 1,
    "CBS-related_disorder|Homocystinuria|not_provided|Classic_homocystinuria|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria": 1,
    "not_specified|Classic_homocystinuria|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Classic_homocystinuria|Homocystinuria": 1,
    "CBS-related_disorder|Classic_homocystinuria": 1,
    "Connective_tissue_disorder|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_specified|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Intellectual_disability": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Classic_homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Homocystinuria|Classic_homocystinuria": 1,
    "Homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Classic_homocystinuria": 1,
    "Homocystinuria|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "CBS-related_disorder|not_provided|Homocystinuria|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Homocystinuria|_pyridoxine-responsive|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Cardiovascular_phenotype|CBS-related_disorder|Homocystinuria|not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder": 1,
    "CBS-related_disorder|Homocystinuria|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_specified|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified": 1,
    "Connective_tissue_disorder|CBS-related_disorder|not_specified|not_provided|Classic_homocystinuria|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "not_provided|Homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Classic_homocystinuria": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|not_specified": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified": 1,
    "not_provided|Classic_homocystinuria|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_specified|CBS-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Cardiovascular_phenotype": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|Classic_homocystinuria|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|not_provided|Classic_homocystinuria": 1,
    "HYPERHOMOCYSTEINEMIA|_THROMBOTIC|_CBS-RELATED|CBS-related_disorder|Classic_homocystinuria|Homocystinuria|not_provided": 1,
    "Classic_homocystinuria|not_specified": 1,
    "U2AF1-related_disorder": 1,
    "Cataract_9_multiple_types": 42,
    "not_provided|not_specified|Cataract_9_multiple_types": 2,
    "Cataract_9|_autosomal_recessive|not_provided": 1,
    "not_provided|Cataract_9|_multiple_types|_with_microcornea|Developmental_cataract|Cataract_9_multiple_types|Abnormality_of_the_eye": 1,
    "not_specified|Cataract_9_multiple_types": 2,
    "Cataract_9|_multiple_types|_with_microcornea|Developmental_cataract|CRYAA-related_disorder|Cataract_9_multiple_types|not_provided": 1,
    "CRYAA-related_disorder|Cataract_9_multiple_types|not_provided": 1,
    "Developmental_cataract|Cataract_9_multiple_types": 1,
    "Cataract_9_multiple_types|not_specified": 4,
    "not_provided|Cataract_9_multiple_types": 5,
    "not_provided|Cataract_9_multiple_types|CRYAA-related_disorder|not_specified": 1,
    "CRYAA-related_disorder|not_provided": 1,
    "CRYAA-related_disorder": 2,
    "Cataract_9_multiple_types|not_provided": 5,
    "not_specified|not_provided|Cataract_9_multiple_types": 2,
    "Cataract_9_multiple_types|not_provided|Cataract_9|_multiple_types|_with_microcornea|CRYAA-related_disorder": 1,
    "Cataract_9_multiple_types|Developmental_cataract|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_30": 731,
    "not_provided|Developmental_and_epileptic_encephalopathy|_30": 21,
    "Developmental_and_epileptic_encephalopathy|_30|not_provided": 33,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30": 87,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30|not_provided": 12,
    "Developmental_and_epileptic_encephalopathy|_30|not_provided|Inborn_genetic_diseases": 11,
    "Developmental_and_epileptic_encephalopathy|_30|Inborn_genetic_diseases": 32,
    "Seizure|Developmental_and_epileptic_encephalopathy|_30": 1,
    "Developmental_and_epileptic_encephalopathy|_30|Inborn_genetic_diseases|not_provided": 13,
    "Developmental_and_epileptic_encephalopathy|_30|not_specified": 7,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30": 8,
    "not_specified|Developmental_and_epileptic_encephalopathy|_30": 4,
    "not_provided|Developmental_and_epileptic_encephalopathy|_30|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_30": 5,
    "not_provided|Developmental_and_epileptic_encephalopathy|_30|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_30": 1,
    "Language_disorder|Global_developmental_delay": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30": 2,
    "Developmental_and_epileptic_encephalopathy|_30|not_provided|not_specified": 3,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_30|not_specified": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_30|Inborn_genetic_diseases": 1,
    "Premature_ovarian_failure_19": 3,
    "PDXK-related_disorder|not_provided": 4,
    "PDXK-related_disorder": 4,
    "Neuropathy|_hereditary_motor_and_sensory|_type_VIc|_with_optic_atrophy": 3,
    "not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_VIc|_with_optic_atrophy": 2,
    "Neuropathy|_hereditary_motor_and_sensory|_type_VIc|_with_optic_atrophy|not_provided": 1,
    "PDXK-related_disorder|not_provided|Neuropathy|_hereditary_motor_and_sensory|_type_VIc|_with_optic_atrophy": 1,
    "PDXK-related_disorder|Neuropathy|_hereditary_motor_and_sensory|_type_VIc|_with_optic_atrophy": 1,
    "not_provided|PDXK-related_disorder": 2,
    "not_specified|Neuropathy|_hereditary_motor_and_sensory|_type_VIc|_with_optic_atrophy": 1,
    "Unverricht-Lundborg_syndrome": 20,
    "not_provided|Unverricht-Lundborg_syndrome": 4,
    "Unverricht-Lundborg_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|not_provided|Unverricht-Lundborg_syndrome": 2,
    "CSTB-related_disorder": 1,
    "Aplasia/Hypoplasia_of_the_corpus_callosum|Progressive_microcephaly|Dyskinesia|Motor_delay|Intellectual_disability|_severe|Severe_global_developmental_delay|Global_brain_atrophy|Dystonic_disorder|Self-limited_epilepsy_with_centrotemporal_spikes|Unverricht-Lundborg_syndrome|Progressive_myoclonic_epilepsy|not_provided": 1,
    "not_specified|Progressive_myoclonic_epilepsy|Unverricht-Lundborg_syndrome": 1,
    "Progressive_myoclonic_epilepsy|Unverricht-Lundborg_syndrome": 4,
    "Progressive_myoclonic_epilepsy|Unverricht-Lundborg_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "CSTB-related_disorder|Unverricht-Lundborg_syndrome|Inborn_genetic_diseases|not_provided|Progressive_myoclonic_epilepsy|not_specified": 1,
    "Progressive_myoclonic_epilepsy|CSTB-related_disorder": 2,
    "Microcephaly|Cerebral_dysmyelination|Encephalopathy|Inborn_genetic_diseases|Chorea|Dyskinesia|not_provided|Progressive_myoclonic_epilepsy|Unverricht-Lundborg_syndrome": 1,
    "Progressive_myoclonic_epilepsy|not_provided|Inborn_genetic_diseases|Unverricht-Lundborg_syndrome|not_specified": 1,
    "not_provided|Unverricht-Lundborg_syndrome|Progressive_myoclonic_epilepsy": 1,
    "Inborn_genetic_diseases|Progressive_myoclonic_epilepsy|Unverricht-Lundborg_syndrome|not_specified|not_provided": 1,
    "Unverricht-Lundborg_syndrome|not_specified": 2,
    "Neurodevelopmental_disorder_with_microcephaly|_short_stature|_and_speech_delay": 5,
    "TRAPPC10-related_disorder": 3,
    "Intellectual_disability|Neurodevelopmental_disorder_with_microcephaly|_short_stature|_and_speech_delay": 1,
    "TRAPPopathy_microcephalic": 1,
    "NEURODEVELOPMENTAL_DISORDER_WITH_MICROCEPHALY|_SHORT_STATURE|_SPEECH_DELAY|_AND_BEHAVIORAL_ABNORMALITIES": 1,
    "Neurodevelopmental_disorder_with_microcephaly|_short_stature|_and_speech_delay|not_specified": 1,
    "not_provided|Immunodeficiency_119": 1,
    "Polyglandular_autoimmune_syndrome|_type_1": 980,
    "not_provided|Polyglandular_autoimmune_syndrome|_type_1": 32,
    "Polyglandular_autoimmune_syndrome|_type_1|Inherited_Immunodeficiency_Diseases": 1,
    "Inborn_genetic_diseases|Polyglandular_autoimmune_syndrome|_type_1": 19,
    "Polyglandular_autoimmune_syndrome|_type_1|not_provided": 31,
    "AIRE-related_disorder|not_provided|Polyglandular_autoimmune_syndrome|_type_1": 2,
    "Polyglandular_autoimmune_syndrome|_type_1|not_specified|not_provided": 6,
    "not_specified|Polyglandular_autoimmune_syndrome|_type_1|not_provided": 7,
    "Inborn_genetic_diseases|Polyglandular_autoimmune_syndrome|_type_1|AIRE-related_disorder": 1,
    "Polyglandular_autoimmune_syndrome|_type_1|AIRE-related_disorder": 15,
    "AIRE-related_disorder|Inborn_genetic_diseases|Polyglandular_autoimmune_syndrome|_type_1": 2,
    "Polyglandular_autoimmune_syndrome|_type_1|Inborn_genetic_diseases": 18,
    "Polyglandular_autoimmune_syndrome|_type_1|Inborn_genetic_diseases|not_specified": 2,
    "Polyglandular_autoimmune_syndrome|_type_1|not_specified": 12,
    "not_specified|Polyglandular_autoimmune_syndrome|_type_1": 9,
    "AIRE-related_disorder|Polyglandular_autoimmune_syndrome|_type_1": 11,
    "Polyglandular_autoimmune_syndrome|_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Polyglandular_autoimmune_syndrome|_type_1|AIRE-related_disorder": 4,
    "not_provided|Polyglandular_autoimmune_syndrome|_type_1|not_specified": 3,
    "Inborn_genetic_diseases|not_specified|AIRE-related_disorder|Polyglandular_autoimmune_syndrome|_type_1": 1,
    "not_specified|not_provided|Polyglandular_autoimmune_syndrome|_type_1": 10,
    "not_provided|Polyglandular_autoimmune_syndrome|_type_1|Inborn_genetic_diseases": 3,
    "not_provided|AIRE-related_disorder|Polyglandular_autoimmune_syndrome|_type_1": 3,
    "AIRE-related_disorder": 5,
    "not_provided|not_specified|Polyglandular_autoimmune_syndrome|_type_1": 3,
    "Autoimmune_polyglandular_syndrome_type_1|_autosomal_dominant": 1,
    "Polyglandular_autoimmune_syndrome|_type_1|not_provided|not_specified": 1,
    "AIRE-related_disorder|Inborn_genetic_diseases|not_provided|Polyglandular_autoimmune_syndrome|_type_1": 1,
    "Polyglandular_autoimmune_syndrome|_type_1|Autoimmune_polyglandular_syndrome_type_1|_with_reversible_metaphyseal_dysplasia": 1,
    "not_specified|Polyglandular_autoimmune_syndrome|_type_1|Inborn_genetic_diseases|AIRE-related_disorder": 1,
    "Polyglandular_autoimmune_syndrome|_type_1|AIRE-related_disorder|not_provided": 1,
    "AIRE-related_disorder|not_provided|Polyglandular_autoimmune_syndrome|_type_1|Autoimmune_polyglandular_syndrome_type_1|_with_reversible_metaphyseal_dysplasia": 1,
    "not_provided|AIRE-related_disorder|Polyglandular_autoimmune_syndrome|_type_1|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Polyglandular_autoimmune_syndrome|_type_1": 2,
    "Polyglandular_autoimmune_syndrome|_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Polyglandular_autoimmune_syndrome|_type_1|AIRE-related_disorder|Inborn_genetic_diseases": 1,
    "Polyglandular_autoimmune_syndrome|_type_1|not_provided|AIRE-related_disorder|not_specified": 1,
    "not_provided|Polyglandular_autoimmune_syndrome|_type_1|AIRE-related_disorder|not_specified": 1,
    "AIRE-related_disorder|not_specified|not_provided|Polyglandular_autoimmune_syndrome|_type_1": 1,
    "PFKL-related_disorder": 8,
    "not_provided|PFKL-related_disorder": 1,
    "PFKL-related_disorder|not_specified|not_provided": 1,
    "CFAP410-related_disorder": 18,
    "CFAP410-related_disorder|not_provided": 22,
    "not_provided|CFAP410-related_disorder": 15,
    "Axial_spondylometaphyseal_dysplasia": 5,
    "Retinitis_pigmentosa|Axial_spondylometaphyseal_dysplasia": 1,
    "not_provided|CFAP410-related_disorder|not_specified": 1,
    "Retinal_dystrophy_with_or_without_macular_staphyloma": 10,
    "not_provided|Axial_spondylometaphyseal_dysplasia": 1,
    "Retinal_dystrophy_with_or_without_macular_staphyloma|not_provided": 3,
    "Retinal_dystrophy_with_or_without_macular_staphyloma|Retinal_dystrophy|not_provided": 1,
    "not_provided|CFAP410-related_disorder|Retinal_dystrophy_with_or_without_macular_staphyloma": 1,
    "Axial_spondylometaphyseal_dysplasia|Retinal_dystrophy_with_or_without_macular_staphyloma|not_provided": 1,
    "Retinal_dystrophy|not_provided|Axial_spondylometaphyseal_dysplasia": 1,
    "Retinal_dystrophy_with_or_without_macular_staphyloma|Axial_spondylometaphyseal_dysplasia": 1,
    "Retinal_dystrophy|Retinal_dystrophy_with_or_without_macular_staphyloma|not_provided": 2,
    "Retinal_dystrophy_with_or_without_macular_staphyloma|not_provided|See_cases": 1,
    "Cone_dystrophy|Axial_spondylometaphyseal_dysplasia|Retinal_dystrophy_with_or_without_macular_staphyloma|not_provided|Retinitis_pigmentosa|CFAP410-related_disorder|Retinal_dystrophy": 1,
    "Retinal_dystrophy_with_or_without_macular_staphyloma|not_specified": 1,
    "not_provided|Retinal_dystrophy_with_or_without_macular_staphyloma": 1,
    "Axial_spondylometaphyseal_dysplasia|not_provided": 1,
    "Axial_spondylometaphyseal_dysplasia|Retinal_dystrophy_with_or_without_macular_staphyloma|not_provided|Retinal_dystrophy|Retinitis_pigmentosa|CFAP410-related_disorder": 1,
    "not_provided|TSPEAR-related_disorder": 7,
    "Tooth_agenesis|_selective|_10|Autosomal_recessive_nonsyndromic_hearing_loss_98|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 3,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Tooth_agenesis|_selective|_10|Autosomal_recessive_nonsyndromic_hearing_loss_98|TSPEAR-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Tooth_agenesis|_selective|_10": 4,
    "Autosomal_recessive_nonsyndromic_hearing_loss_98|Tooth_agenesis|_selective|_10|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 1,
    "not_provided|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Tooth_agenesis|_selective|_10|TSPEAR-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_98": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_98|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Tooth_agenesis|_selective|_10": 3,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_98": 3,
    "not_specified|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|not_provided": 4,
    "TSPEAR-related_disorder|not_provided": 5,
    "Autosomal_recessive_nonsyndromic_hearing_loss_98|Tooth_agenesis|_selective|_10|Ectodermal_dysplasia_14|_hair/tooth_type|_with_hypohidrosis": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|not_provided|TSPEAR-related_disorder_of_tooth_and_hair_follicle_morphogenesis": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Autosomal_recessive_nonsyndromic_hearing_loss_98|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|TSPEAR-related_disorder|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 7,
    "not_provided|not_specified|TSPEAR-related_disorder": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|TSPEAR-related_disorder|Inborn_genetic_diseases|Tooth_agenesis|_selective|_10|not_specified|not_provided": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Autosomal_recessive_nonsyndromic_hearing_loss_98|TSPEAR-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_98|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Tooth_agenesis|_selective|_10|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_98|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_98|Tooth_agenesis|_selective|_10|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 1,
    "not_provided|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 2,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Tooth_agenesis|_selective|_10|Autosomal_recessive_nonsyndromic_hearing_loss_98": 1,
    "not_provided|Tooth_agenesis|_selective|_10": 2,
    "Tooth_agenesis|_selective|_10|not_provided": 1,
    "TSPEAR-related_disorder": 5,
    "not_specified|TSPEAR-related_disorder|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|TSPEAR-related_disorder": 2,
    "Inborn_genetic_diseases|TSPEAR-related_disorder|not_provided": 1,
    "not_provided|Tooth_agenesis|_selective|_10|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 1,
    "TSPEAR-related_disorder|not_specified|not_provided": 4,
    "not_provided|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Inborn_genetic_diseases|not_specified|TSPEAR-related_disorder|TSPEAR-related_disorder_of_tooth_and_hair_follicle_morphogenesis": 1,
    "Ectodermal_dysplasia_14|_hair/tooth_type|_with_hypohidrosis": 1,
    "not_specified|not_provided|TSPEAR-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_98|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_98|Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis": 1,
    "Inborn_genetic_diseases|not_provided|TSPEAR-related_disorder": 1,
    "Inborn_genetic_diseases|TSPEAR-related_disorder|not_specified|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_98": 2,
    "Ectodermal_dysplasia_14|_hair/tooth_type_with_or_without_hypohidrosis|Breast_ductal_adenocarcinoma": 1,
    "TSPEAR-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "TSPEAR-related_disorder|not_provided|not_specified": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_98|not_provided|not_specified": 1,
    "TSPEAR-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_98": 1,
    "Leukocyte_adhesion_deficiency_1": 633,
    "Leukocyte_adhesion_deficiency": 2,
    "not_provided|Leukocyte_adhesion_deficiency": 1,
    "not_provided|Leukocyte_adhesion_deficiency_1": 21,
    "Leukocyte_adhesion_deficiency_1|not_provided": 21,
    "Leukocyte_adhesion_deficiency_1|Inborn_genetic_diseases": 26,
    "Leukocyte_adhesion_deficiency_1|not_provided|not_specified": 5,
    "Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_1": 34,
    "Leukocyte_adhesion_deficiency_1|ITGB2-related_disorder|not_specified": 1,
    "ITGB2-related_disorder|Leukocyte_adhesion_deficiency_1": 14,
    "not_specified|not_provided|Leukocyte_adhesion_deficiency_1": 2,
    "Leukocyte_adhesion_deficiency_1|ITGB2-related_disorder": 5,
    "Leukocyte_adhesion_deficiency_1|not_provided|ITGB2-related_disorder": 4,
    "ITGB2-related_disorder|not_provided|not_specified|Leukocyte_adhesion_deficiency_1": 1,
    "ITGB2-related_disorder|not_provided|Leukocyte_adhesion_deficiency_1": 1,
    "Leukocyte_adhesion_deficiency_1|not_specified|not_provided": 3,
    "not_specified|Leukocyte_adhesion_deficiency_1|not_provided": 2,
    "ITGB2-related_disorder|Leukocyte_adhesion_deficiency_1|not_provided": 2,
    "Inborn_genetic_diseases|Leukocyte_adhesion_deficiency_1|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Leukocyte_adhesion_deficiency_1": 2,
    "Leukocyte_adhesion_deficiency_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Leukocyte_adhesion_deficiency_1|Inborn_genetic_diseases": 1,
    "ITGB2-related_disorder": 1,
    "not_provided|Leukocyte_adhesion_deficiency_1|not_specified": 1,
    "not_provided|not_specified|Leukocyte_adhesion_deficiency_1": 3,
    "Leukocyte_adhesion_deficiency_1|Leukocyte_adhesion_deficiency_3|not_provided": 1,
    "ADARB1-related_disorder": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_microcephaly|_and_seizures|Syndromic_intellectual_disability": 2,
    "Neurodevelopmental_disorder_with_hypotonia|_microcephaly|_and_seizures|Inborn_genetic_diseases": 1,
    "Neurodevelopmental_disorder_with_hypotonia|_microcephaly|_and_seizures|not_provided": 1,
    "Abnormal_CNS_myelination|Microcephaly|Encephalopathy": 1,
    "Knobloch_syndrome|not_specified": 1,
    "not_provided|Knobloch_syndrome|COL18A1-related_disorder|Knobloch_syndrome_1": 1,
    "not_provided|Knobloch_syndrome|COL18A1-related_disorder": 4,
    "not_provided|COL18A1-related_disorder": 36,
    "COL18A1-related_disorder|not_provided": 47,
    "Knobloch_syndrome|not_provided|Hereditary_glaucoma|_primary_closed-angle": 1,
    "COL18A1-related_disorder|not_specified|not_provided": 2,
    "not_provided|Knobloch_syndrome_1": 6,
    "not_specified|COL18A1-related_disorder|not_provided": 1,
    "COL18A1-related_disorder|Knobloch_syndrome_1|not_provided": 1,
    "COL18A1-related_disorder|Inborn_genetic_diseases|not_specified|Knobloch_syndrome|not_provided": 1,
    "COL18A1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Hereditary_glaucoma|_primary_closed-angle": 1,
    "Knobloch_syndrome|not_provided|Inborn_genetic_diseases|Hereditary_glaucoma|_primary_closed-angle": 1,
    "Inborn_genetic_diseases|COL18A1-related_disorder|not_provided": 2,
    "COL18A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome|not_specified": 2,
    "COL18A1-related_disorder": 34,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome|not_provided": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|not_provided": 6,
    "COL18A1-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Knobloch_syndrome|not_provided": 4,
    "Knobloch_syndrome|not_provided": 49,
    "not_specified|Knobloch_syndrome|not_provided": 7,
    "Hereditary_glaucoma|_primary_closed-angle|not_provided|Knobloch_syndrome": 1,
    "not_specified|COL18A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "COL18A1-related_disorder|not_provided|Knobloch_syndrome": 3,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "COL18A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Knobloch_syndrome": 1,
    "Knobloch_syndrome|Hereditary_glaucoma|_primary_closed-angle": 1,
    "not_provided|COL18A1-related_disorder|Knobloch_syndrome": 4,
    "not_provided|Knobloch_syndrome|COL18A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Knobloch_syndrome": 1,
    "Inborn_genetic_diseases|Knobloch_syndrome|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|not_provided": 1,
    "early_onset_and_severe_retinal_dystrophy": 5,
    "Knobloch_syndrome_1|Retinal_dystrophy|not_provided": 1,
    "Inborn_genetic_diseases|Knobloch_syndrome|COL18A1-related_disorder|not_provided": 1,
    "Knobloch_syndrome|not_provided|COL18A1-related_disorder": 2,
    "Inborn_genetic_diseases|COL18A1-related_disorder|Knobloch_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Knobloch_syndrome_1": 1,
    "not_provided|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1": 4,
    "Knobloch_syndrome_1|not_provided": 10,
    "not_provided|COL18A1-related_disorder|not_specified": 1,
    "not_specified|not_provided|Knobloch_syndrome|COL18A1-related_disorder": 1,
    "not_provided|Knobloch_syndrome|not_specified": 4,
    "Inborn_genetic_diseases|Hereditary_glaucoma|_primary_closed-angle|not_provided": 1,
    "not_specified|not_provided|Knobloch_syndrome": 5,
    "not_provided|Retinal_dystrophy|Cataract|High_myopia|Nystagmus": 2,
    "Hereditary_glaucoma|_primary_closed-angle|not_provided": 1,
    "not_provided|Knobloch_syndrome|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|not_provided": 1,
    "COL18A1-related_disorder|Inborn_genetic_diseases|not_provided": 8,
    "Inborn_genetic_diseases|not_provided|COL18A1-related_disorder": 1,
    "Knobloch_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Knobloch_syndrome_1|Knobloch_syndrome|not_provided": 1,
    "not_specified|not_provided|COL18A1-related_disorder": 1,
    "not_specified|Knobloch_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle|not_provided|Knobloch_syndrome": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome|not_provided|not_specified": 1,
    "not_specified|COL18A1-related_disorder|Knobloch_syndrome|not_provided": 1,
    "COL18A1-related_disorder|not_provided|Knobloch_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Ocular_motility_disease|Knobloch_syndrome": 1,
    "not_provided|COL18A1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Knobloch_syndrome": 1,
    "COL18A1-related_disorder|Knobloch_syndrome|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|COL18A1-related_disorder|Knobloch_syndrome": 1,
    "COL18A1-related_disorder|not_specified|Knobloch_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Knobloch_syndrome": 5,
    "not_provided|Inborn_genetic_diseases|COL18A1-related_disorder": 2,
    "not_specified|Hereditary_glaucoma|_primary_closed-angle|not_provided|Knobloch_syndrome": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle|not_provided": 1,
    "Knobloch_syndrome|COL18A1-related_disorder|not_provided": 2,
    "Knobloch_syndrome|not_provided|Hereditary_glaucoma|_primary_closed-angle|not_specified": 1,
    "Knobloch_syndrome|not_specified|not_provided": 2,
    "Knobloch_syndrome|not_provided|Retinal_dystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Knobloch_syndrome": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Knobloch_syndrome": 1,
    "Knobloch_syndrome_1|not_provided|Knobloch_syndrome": 1,
    "COL18A1-related_disorder|not_provided|not_specified": 1,
    "Knobloch_syndrome|not_provided|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1": 1,
    "Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle|not_specified|not_provided": 1,
    "Knobloch_syndrome|not_provided|not_specified": 2,
    "Knobloch_syndrome|COL18A1-related_disorder|not_provided|not_specified": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome": 1,
    "Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle": 1,
    "Inborn_genetic_diseases|Knobloch_syndrome": 2,
    "not_provided|Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle": 1,
    "Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle|not_provided": 2,
    "Inborn_genetic_diseases|Knobloch_syndrome_1|Knobloch_syndrome": 1,
    "Knobloch_syndrome|not_provided|not_specified|COL18A1-related_disorder": 1,
    "Knobloch_syndrome_1|Knobloch_syndrome": 1,
    "not_provided|COL18A1-related_disorder|Hereditary_glaucoma|_primary_closed-angle|Progressive_neurodegenerative_disease": 1,
    "COL18A1-related_disorder|Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle|not_specified|not_provided": 1,
    "Knobloch_syndrome_1|Hereditary_glaucoma|_primary_closed-angle|COL18A1-related_disorder|not_provided": 1,
    "not_provided|not_specified|COL18A1-related_disorder": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|not_specified|not_provided": 1,
    "Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|Macular_dystrophy|Retinal_dystrophy|not_provided|Knobloch_syndrome|Retinitis_pigmentosa": 1,
    "Cowden_syndrome_1|Knobloch_syndrome": 1,
    "Knobloch_syndrome|COL18A1-related_disorder|Knobloch_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|COL18A1-related_disorder": 1,
    "COL18A1-related_disorder|Hereditary_glaucoma|_primary_closed-angle|Knobloch_syndrome_1|not_provided": 1,
    "not_specified|not_provided|Knobloch_syndrome_1|Knobloch_syndrome": 1,
    "Hereditary_glaucoma|_primary_closed-angle": 1,
    "SLC19A1-related_disorder": 3,
    "not_provided|SLC19A1-related_disorder": 5,
    "SLC19A1-related_disorder|not_provided": 3,
    "Immunodeficiency_114|_folate-responsive": 1,
    "not_provided|Megaloblastic_anemia|_folate-responsive": 1,
    "Megaloblastic_anemia|_folate-responsive|not_provided|not_specified": 1,
    "Lung_cancer|not_provided|Gastrointestinal_stromal_tumor|methotrexate_response_-_Efficacy": 1,
    "PCBP3-related_disorder|not_provided": 1,
    "PCBP3-related_disorder": 7,
    "not_provided|PCBP3-related_disorder": 1,
    "not_specified|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "COL6A1-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 3,
    "not_provided|COL6A1-related_disorder|Bethlem_myopathy_1A": 2,
    "Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A": 2,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1A|COL6A1-related_disorder": 7,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Inborn_genetic_diseases": 1,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Inborn_genetic_diseases": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "not_provided|Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|not_specified|Bethlem_myopathy_1A|not_provided": 1,
    "COL6A1-related_disorder|Bethlem_myopathy_1A|not_provided": 5,
    "Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A|not_specified|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Inborn_genetic_diseases": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|not_specified|COL6A1-related_disorder": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_specified|not_provided": 1,
    "COL6A1-related_disorder|not_provided|Bethlem_myopathy_1A": 3,
    "Bethlem_myopathy_1A|COL6A1-related_disorder|not_provided": 2,
    "Bethlem_myopathy_1A|not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 2,
    "ULLRICH_CONGENITAL_MUSCULAR_DYSTROPHY_1A|_AUTOSOMAL_DOMINANT": 1,
    "not_provided|Motor_delay|EMG_abnormality|Limb-girdle_muscle_weakness": 1,
    "ULLRICH_CONGENITAL_MUSCULAR_DYSTROPHY_1A|_AUTOSOMAL_DOMINANT|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "COL6A1-related_disorder": 8,
    "Bethlem_myopathy_1A|not_specified|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Abnormality_of_the_musculature": 1,
    "Bethlem_myopathy_1A|ULLRICH_CONGENITAL_MUSCULAR_DYSTROPHY_1A|_AUTOSOMAL_DOMINANT": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|COL6A1-related_disorder|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|not_provided|not_specified|Bethlem_myopathy_1A": 1,
    "COL6A1-related_disorder|not_provided": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 4,
    "not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "COL6A1-related_disorder|Bethlem_myopathy_1A": 4,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|COL6A1-related_disorder": 1,
    "COL6A1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Myopathy": 1,
    "Bethlem_myopathy_1A|Abnormality_of_the_musculature|not_provided|Sensorimotor_neuropathy": 1,
    "Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_specified": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Bethlem_myopathy_1A|not_provided|COL6A1-related_disorder": 3,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Collagen_6-related_myopathy|not_provided|not_specified|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|not_provided|Ullrich_congenital_muscular_dystrophy_1A|not_specified": 1,
    "not_specified|Bethlem_myopathy_1A|not_provided|COL6A1-related_disorder": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|not_provided|Bethlem_myopathy_1A|not_specified": 1,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified": 2,
    "Bethlem_myopathy_1B|not_provided": 1,
    "COL6A1-related_disorder|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Inborn_genetic_diseases|not_provided": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Collagen_6-related_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Inborn_genetic_diseases": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified": 3,
    "COL6A1-related_disorder|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_provided": 1,
    "COL6A1-related_disorder|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|COL6A1-related_disorder": 1,
    "COL6A1-related_disorder|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided|Ullrich_congenital_muscular_dystrophy_1A|not_specified": 1,
    "not_provided|not_specified|Bethlem_myopathy_1A|COL6A1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Bethlem_myopathy_1A|not_specified": 2,
    "Bethlem_myopathy_1A|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Bethlem_myopathy_1A|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided|Inborn_genetic_diseases": 1,
    "Collagen_6-related_myopathy|Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A|Ehlers-Danlos_syndrome": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "not_specified|Bethlem_myopathy_1A|COL6A1-related_disorder|not_provided": 1,
    "COL6A1-related_disorder|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "not_provided|Collagen_6-related_myopathy|Inborn_genetic_diseases|Bethlem_myopathy_1A": 1,
    "COL6A1-related_disorder|not_specified|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "COL6A1-related_disorder|Inborn_genetic_diseases|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 1,
    "COL6A1-related_disorder|not_provided|Bethlem_myopathy_1A|not_specified": 1,
    "Bethlem_myopathy_1A|Inborn_genetic_diseases|Collagen_6-related_myopathy": 2,
    "Bethlem_myopathy_1A|not_provided|not_specified|Collagen_6-related_myopathy": 1,
    "Collagen_6-related_myopathy|not_specified|not_provided": 1,
    "not_specified|Collagen_6-related_myopathy|not_provided": 1,
    "COL6A2-related_disorder": 28,
    "Bethlem_myopathy_1A|Myosclerosis": 2,
    "not_specified|not_provided|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 4,
    "Myosclerosis|Collagen_6-related_myopathy|not_provided|not_specified|COL6A2-related_disorder|Bethlem_myopathy_1A": 2,
    "Myosclerosis|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "COL6A2-related_disorder|Bethlem_myopathy_1A|not_provided": 9,
    "Myosclerosis|Collagen_6-related_myopathy": 4,
    "COL6A2-related_disorder|not_provided|Bethlem_myopathy_1A": 4,
    "not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy|COL6A2-related_disorder|Myosclerosis": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Myosclerosis|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 6,
    "COL6A2-related_disorder|not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided": 1,
    "not_provided|COL6A2-related_disorder|Bethlem_myopathy_1A|not_specified": 1,
    "Ullrich_congenital_muscular_dystrophy_1B": 10,
    "Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis|Bethlem_myopathy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "not_provided|Inborn_genetic_diseases|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis": 1,
    "COL6A2-related_disorder|Bethlem_myopathy_1A": 12,
    "Bethlem_myopathy_1A|Myosclerosis|Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B|not_provided": 1,
    "Inborn_genetic_diseases|Collagen_6-related_myopathy|Bethlem_myopathy_1A|COL6A2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Collagen_6-related_myopathy|Limb-girdle_muscular_dystrophy|Bethlem_myopathy_1A": 1,
    "not_specified|not_provided|Myosclerosis|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 4,
    "Bethlem_myopathy_1A|COL6A2-related_disorder": 11,
    "COL6A2-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 2,
    "COL6A2-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 2,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|Myosclerosis|Ullrich_congenital_muscular_dystrophy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "COL6A2-related_disorder|not_provided|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A|Tip-toe_gait": 1,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis|not_specified": 1,
    "Collagen_6-related_myopathy|Myosclerosis": 9,
    "Inborn_genetic_diseases|Collagen_6-related_myopathy|not_provided|Myosclerosis|Bethlem_myopathy_1A": 1,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 2,
    "Bethlem_myopathy_1B": 2,
    "Myosclerosis|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided": 1,
    "Bethlem_myopathy_1A|Myosclerosis|not_provided|Collagen_6-related_myopathy": 1,
    "Collagen_6-related_myopathy|Myosclerosis|not_provided|Bethlem_myopathy_1A|not_specified": 1,
    "Bethlem_myopathy_1A|Myosclerosis|Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B": 1,
    "Collagen_6-related_myopathy|Myosclerosis|not_specified|Bethlem_myopathy_1A|not_provided": 1,
    "Fatigue|Muscular_dystrophy|Limb-girdle_muscle_weakness|Hyperextensible_hand_joints|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis|Tip-toe_gait": 1,
    "BETHLEM_MYOPATHY_1B|_AUTOSOMAL_RECESSIVE": 2,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis": 2,
    "not_provided|Bethlem_myopathy_1A|Abnormality_of_the_musculature": 1,
    "Bethlem_myopathy_1A|COL6A2-related_core_myopathy": 1,
    "Bethlem_myopathy_1B|not_provided|Bethlem_myopathy_1A": 2,
    "COL6A2-related_disorder|not_provided": 2,
    "Bethlem_myopathy_1A|not_provided|Ullrich_congenital_muscular_dystrophy_1B|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Bethlem_myopathy_1A|Bethlem_myopathy_1B|not_provided": 1,
    "Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 4,
    "Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B": 2,
    "Myosclerosis|COL6A2-related_disorder|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "not_provided|Ullrich_congenital_muscular_dystrophy_1A|not_specified|Myosclerosis|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|Inborn_genetic_diseases|not_provided": 1,
    "Bethlem_myopathy_1B|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1B|Bethlem_myopathy_1B|Myosclerosis|not_provided|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis|Tip-toe_gait": 1,
    "Bethlem_myopathy_1A|COL6A2-related_disorder|not_provided": 4,
    "Bethlem_myopathy_1A|Bethlem_myopathy_1B": 2,
    "Inborn_genetic_diseases|Myosclerosis|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|Inborn_genetic_diseases|not_specified": 1,
    "Bethlem_myopathy|Abnormality_of_the_musculature|Bethlem_myopathy_1A|Myosclerosis|Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B": 1,
    "COL6A2-related_disorder|not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 1,
    "Myosclerosis|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "BETHLEM_MYOPATHY_1B|_AUTOSOMAL_RECESSIVE|not_provided|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided": 1,
    "not_specified|not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_specified|Myosclerosis|not_provided": 1,
    "not_specified|not_provided|COL6A2-related_disorder|Bethlem_myopathy_1A": 1,
    "not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 1,
    "Charcot-Marie-Tooth_disease|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis|Bethlem_myopathy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "COL6A2-related_disorder|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Myosclerosis|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 3,
    "not_provided|Myosclerosis|Bethlem_myopathy_1A|not_specified|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Myosclerosis|not_provided|Bethlem_myopathy_1A|COL6A2-related_disorder|Collagen_6-related_myopathy": 1,
    "not_specified|Myosclerosis|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Inborn_genetic_diseases|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Collagen_6-related_myopathy|not_specified|not_provided|Myosclerosis": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis": 1,
    "not_provided|COL6A2-related_disorder": 2,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1B": 1,
    "not_provided|Bethlem_myopathy_1A|COL6A2-related_disorder": 2,
    "not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 4,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1B": 1,
    "Bethlem_myopathy_1A|Bethlem_myopathy_1B|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Inborn_genetic_diseases|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis|not_provided": 1,
    "COL6A2-related_disorder|Collagen_6-related_myopathy|not_provided|Myosclerosis|not_specified|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1B|not_provided|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1B": 2,
    "Ullrich_congenital_muscular_dystrophy_1B|not_provided": 1,
    "Myosclerosis": 2,
    "not_specified|Myosclerosis|Collagen_6-related_myopathy|not_provided|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1B|Bethlem_myopathy_1A|not_provided|See_cases|Inborn_genetic_diseases": 1,
    "not_provided|Myosclerosis|Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B|Bethlem_myopathy_1A": 1,
    "not_specified|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "not_provided|Myosclerosis|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy|Myosclerosis": 1,
    "Bethlem_myopathy_1A|not_specified|COL6A2-related_disorder": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified|Myosclerosis|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "Bethlem_myopathy_1A|not_specified|Ullrich_congenital_muscular_dystrophy_1A|not_provided|Myosclerosis": 2,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|not_provided|Myosclerosis": 1,
    "COL6A2-related_disorder|not_specified|Inborn_genetic_diseases|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis": 1,
    "not_provided|COL6A2-related_disorder|Bethlem_myopathy_1A": 2,
    "Collagen_6-related_myopathy|not_specified|not_provided|Myosclerosis|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|not_specified|not_provided|Myosclerosis|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Inborn_genetic_diseases|COL6A2-related_disorder|Bethlem_myopathy_1A|not_provided": 1,
    "not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided|Myosclerosis": 1,
    "Bethlem_myopathy_1A|Myosclerosis|Collagen_6-related_myopathy|not_specified": 1,
    "Myosclerosis|Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|COL6A2-related_disorder": 1,
    "not_provided|Bethlem_myopathy_1A|Bethlem_myopathy_1B": 1,
    "not_provided|Ullrich_congenital_muscular_dystrophy_1B|Bethlem_myopathy_1A": 1,
    "Ullrich_congenital_muscular_dystrophy_1B|Myosclerosis|Bethlem_myopathy_1B": 1,
    "Myosclerosis|Bethlem_myopathy_1A|not_provided": 1,
    "Hip_flexor_weakness|Difficulty_walking|Falls|Muscle_weakness|Congenital_hip_dislocation|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1B|Qualitative_or_quantitative_defects_of_collagen_6|Bethlem_myopathy|Collagen_6-related_myopathy|Abnormality_of_the_musculature": 1,
    "Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1B|Myosclerosis|Bethlem_myopathy_1B|not_specified|not_provided|Limb-girdle_muscular_dystrophy|Collagen_6-related_myopathy|Tip-toe_gait": 1,
    "not_specified|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B|Myosclerosis": 1,
    "Collagen_6-related_myopathy|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|not_specified|Myosclerosis": 1,
    "not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis": 1,
    "Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|not_provided|Inborn_genetic_diseases|Bethlem_myopathy_1A": 2,
    "not_provided|Myosclerosis|Bethlem_myopathy_1A": 1,
    "not_specified|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis|not_specified|not_provided": 1,
    "Bethlem_myopathy|COL6A2-related_disorder|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_provided|Myosclerosis": 1,
    "Myosclerosis|not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified": 1,
    "not_specified|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A|not_provided|Ullrich_congenital_muscular_dystrophy_1A": 1,
    "Inborn_genetic_diseases|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A|Myosclerosis|not_provided": 1,
    "Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy|COL6A2-related_disorder": 2,
    "COL6A2-related_disorder|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis|not_provided": 1,
    "Collagen_6-related_myopathy|Myosclerosis|not_provided": 1,
    "not_provided|Collagen_6-related_myopathy|COL6A2-related_disorder|Myosclerosis|not_specified|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|not_specified|not_provided|Myosclerosis|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A|COL6A2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|COL6A2-related_disorder|Bethlem_myopathy_1A": 1,
    "Myosclerosis|Bethlem_myopathy_1A|not_provided|Collagen_6-related_myopathy": 1,
    "Myosclerosis|Bethlem_myopathy_1A|BETHLEM_MYOPATHY_1B|_AUTOSOMAL_RECESSIVE|not_provided": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis|COL6A2-related_disorder|not_provided": 1,
    "Bethlem_myopathy_1A|not_specified|Myosclerosis|Collagen_6-related_myopathy": 1,
    "Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A|not_provided": 2,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided": 1,
    "Bethlem_myopathy_1B|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_provided|Myopathy": 1,
    "Collagen_6-related_myopathy|Myosclerosis|COL6A2-related_disorder|not_specified|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|not_specified|not_provided|Myosclerosis|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "Collagen_6-related_myopathy|Myosclerosis|not_specified|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Myosclerosis|Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B|Inborn_genetic_diseases": 1,
    "COL6A2-related_disorder|Myosclerosis|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "COL6A2-related_disorder|not_provided|not_specified|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|not_provided|Myosclerosis|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|Myosclerosis|Collagen_6-related_myopathy": 1,
    "Congenital_myopathy|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 1,
    "Collagen_6-related_myopathy|Myosclerosis|not_provided|Bethlem_myopathy_1A": 1,
    "not_provided|Glutamate_formiminotransferase_deficiency|not_specified|Myosclerosis|Bethlem_myopathy_1A|Collagen_6-related_myopathy": 1,
    "COL6A2-related_disorder|not_provided|Bethlem_myopathy_1A|not_specified": 1,
    "not_provided|Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis": 1,
    "Collagen_6-related_myopathy|not_specified|Myosclerosis|Bethlem_myopathy_1A|not_provided": 1,
    "Bethlem_myopathy_1A|COL6A2-related_disorder|not_provided|not_specified": 2,
    "BETHLEM_MYOPATHY_1B|_AUTOSOMAL_RECESSIVE|not_provided|Collagen_6-related_myopathy|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "Inborn_genetic_diseases|Collagen_6-related_myopathy|not_provided|Ullrich_congenital_muscular_dystrophy_1A|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|Inborn_genetic_diseases|not_provided|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Myopathy": 1,
    "Collagen_6-related_myopathy|not_provided|Myosclerosis|Bethlem_myopathy_1A": 2,
    "COL6A2-related_disorder|not_provided|not_specified|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "not_provided|Bethlem_myopathy_1A|not_specified|Collagen_6-related_myopathy": 1,
    "not_specified|COL6A2-related_disorder|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_specified|Myosclerosis|Glutamate_formiminotransferase_deficiency|not_provided": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|Myosclerosis|not_provided": 1,
    "Bethlem_myopathy_1A|Glutamate_formiminotransferase_deficiency|Collagen_6-related_myopathy|Myosclerosis|not_specified|not_provided": 1,
    "Ullrich_congenital_muscular_dystrophy_1B|Ullrich_congenital_muscular_dystrophy_1A|not_provided|Bethlem_myopathy_1A": 1,
    "COL6A2-related_disorder|not_specified|Bethlem_myopathy_1A|not_provided": 1,
    "Bethlem_myopathy_1A|not_provided|not_specified|Myosclerosis|Collagen_6-related_myopathy": 1,
    "not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A": 2,
    "Bethlem_myopathy_1B|COL6A2-related_disorder|not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 1,
    "not_specified|not_provided|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A|Glutamate_formiminotransferase_deficiency": 1,
    "Bethlem_myopathy_1A|not_provided|Bethlem_myopathy_1B|Ullrich_congenital_muscular_dystrophy_1B|Myosclerosis": 1,
    "Bethlem_myopathy_1A|not_provided|COL6A2-related_disorder": 1,
    "Bethlem_myopathy_1A|Myosclerosis|not_specified|not_provided|Collagen_6-related_myopathy": 1,
    "Myosclerosis|Collagen_6-related_myopathy|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|not_provided|Myosclerosis": 2,
    "not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis|COL6A2-related_disorder": 1,
    "COL6A2-related_disorder|Myosclerosis|not_provided|Collagen_6-related_myopathy|not_specified|Bethlem_myopathy_1A": 1,
    "Bethlem_myopathy_1A|Collagen_6-related_myopathy|not_specified|not_provided|Myosclerosis|Glutamate_formiminotransferase_deficiency": 1,
    "Glutamate_formiminotransferase_deficiency|Myosclerosis|Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|not_specified|Collagen_6-related_myopathy|not_provided": 1,
    "not_provided|not_specified|Collagen_6-related_myopathy|Myosclerosis|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|Inborn_genetic_diseases|Myosclerosis|Bethlem_myopathy_1A": 1,
    "Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1B|Myosclerosis|Bethlem_myopathy_1B": 1,
    "Bethlem_myopathy_1A|Ullrich_congenital_muscular_dystrophy_1A|Myosclerosis|not_provided|Collagen_6-related_myopathy": 1,
    "not_specified|not_provided|Collagen_6-related_myopathy|Bethlem_myopathy_1A|Myosclerosis|Glutamate_formiminotransferase_deficiency": 1,
    "Collagen_6-related_myopathy|not_provided|Myosclerosis|Glutamate_formiminotransferase_deficiency": 1,
    "Myosclerosis|not_provided|Collagen_6-related_myopathy": 2,
    "Myosclerosis|Collagen_6-related_myopathy|Glutamate_formiminotransferase_deficiency|not_provided": 1,
    "Collagen_6-related_myopathy|Myosclerosis|not_provided|Glutamate_formiminotransferase_deficiency": 1,
    "Myosclerosis|Collagen_6-related_myopathy|not_provided|Glutamate_formiminotransferase_deficiency": 1,
    "Glutamate_formiminotransferase_deficiency|COL6A2-related_disorder|Collagen_6-related_myopathy|Myosclerosis": 1,
    "Glutamate_formiminotransferase_deficiency": 184,
    "Glutamate_formiminotransferase_deficiency|Collagen_6-related_myopathy|Myosclerosis": 1,
    "FTCD-related_disorder|Glutamate_formiminotransferase_deficiency|Collagen_6-related_myopathy|Myosclerosis": 1,
    "not_provided|Glutamate_formiminotransferase_deficiency": 6,
    "FTCD-related_disorder": 5,
    "Inborn_genetic_diseases|Glutamate_formiminotransferase_deficiency": 19,
    "Glutamate_formiminotransferase_deficiency|not_provided": 9,
    "Glutamate_formiminotransferase_deficiency|Inborn_genetic_diseases": 13,
    "Intellectual_disability|Inborn_genetic_diseases|Glutamate_formiminotransferase_deficiency": 3,
    "Collagen_6-related_myopathy|Myosclerosis|Glutamate_formiminotransferase_deficiency": 1,
    "Collagen_6-related_myopathy|FTCD-related_disorder|Myosclerosis|not_provided|Glutamate_formiminotransferase_deficiency": 1,
    "Inborn_genetic_diseases|Glutamate_formiminotransferase_deficiency|not_provided": 2,
    "not_provided|not_specified|Glutamate_formiminotransferase_deficiency": 2,
    "Inborn_genetic_diseases|not_provided|Glutamate_formiminotransferase_deficiency": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Glutamate_formiminotransferase_deficiency|Intellectual_disability": 1,
    "not_specified|Glutamate_formiminotransferase_deficiency": 1,
    "FTCD-related_disorder|Glutamate_formiminotransferase_deficiency": 1,
    "Glutamate_formiminotransferase_deficiency|FTCD-related_disorder": 3,
    "FTCD-related_disorder|Inborn_genetic_diseases|not_provided|Glutamate_formiminotransferase_deficiency": 1,
    "Myoepithelial_tumor|Inborn_genetic_diseases|not_provided|Glutamate_formiminotransferase_deficiency": 1,
    "Glutamate_formiminotransferase_deficiency|not_provided|FTCD-related_disorder": 2,
    "Glutamate_formiminotransferase_deficiency|not_provided|not_specified": 2,
    "Intellectual_disability|Glutamate_formiminotransferase_deficiency": 3,
    "not_provided|Glutamate_formiminotransferase_deficiency|Inborn_genetic_diseases": 1,
    "FTCD-AS1-related_disorder": 2,
    "not_provided|FTCD-AS1-related_disorder|Glutamate_formiminotransferase_deficiency": 1,
    "Glutamate_formiminotransferase_deficiency|FTCD-AS1-related_disorder": 2,
    "Glutamate_formiminotransferase_deficiency|not_provided|Inborn_genetic_diseases": 2,
    "FTCD-related_disorder|Glutamate_formiminotransferase_deficiency|not_specified|not_provided": 1,
    "FTCD-related_disorder|Glutamate_formiminotransferase_deficiency|Intellectual_disability": 1,
    "FTCD-related_disorder|Glutamate_formiminotransferase_deficiency|not_provided": 1,
    "FTCD-related_disorder|not_provided|Glutamate_formiminotransferase_deficiency": 2,
    "not_provided|Inborn_genetic_diseases|Glutamate_formiminotransferase_deficiency": 1,
    "not_specified|not_provided|Glutamate_formiminotransferase_deficiency": 1,
    "Hypotrichosis_14": 3,
    "not_provided|Hypotrichosis_14": 1,
    "LSS-related_disorder": 3,
    "LSS-related_disorder|not_provided": 9,
    "not_provided|LSS-related_disorder": 3,
    "Cataract_44": 7,
    "not_provided|Cataract_44|Alopecia-intellectual_disability_syndrome_4": 2,
    "Hypotrichosis_14|Cataract_44|Alopecia-intellectual_disability_syndrome_4": 1,
    "not_provided|Cataract_44": 1,
    "not_provided|Alopecia-intellectual_disability_syndrome_4": 2,
    "Alopecia-intellectual_disability_syndrome_4|not_provided|LSS-related_disorder": 1,
    "Hypotrichosis_14|Cataract_44": 1,
    "LSS-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Cataract_44|Alopecia-intellectual_disability_syndrome_4|not_provided": 1,
    "not_provided|Hypotrichosis_14|Alopecia-intellectual_disability_syndrome_4": 1,
    "Cataract_44|Hypotrichosis_14|Alopecia-intellectual_disability_syndrome_4|not_provided": 1,
    "Hypotrichosis_14|Alopecia-intellectual_disability_syndrome_4|not_provided": 1,
    "Alopecia-intellectual_disability_syndrome_4|Cataract_44|not_provided": 2,
    "Cataract_44|Alopecia-intellectual_disability_syndrome_4|Hypotrichosis_14|not_provided": 1,
    "Hypotrichosis_14|Alopecia-intellectual_disability_syndrome_4": 1,
    "not_provided|Hypotrichosis_14|Alopecia-intellectual_disability_syndrome_4|Cataract_44": 1,
    "Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development|not_provided": 5,
    "Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development": 23,
    "not_provided|MCM3AP-related_disorder": 9,
    "not_provided|Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development": 9,
    "not_provided|Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development|Inborn_genetic_diseases": 1,
    "MCM3AP-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "MCM3AP-related_disorder": 1,
    "not_specified|Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development|not_provided": 1,
    "MCM3AP-related_disorder|not_provided": 10,
    "Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development|Inborn_genetic_diseases|not_provided": 3,
    "Inborn_genetic_diseases|MCM3AP-related_disorder|not_provided|Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development": 1,
    "not_provided|Peripheral_neuropathy|_autosomal_recessive|_with_or_without_impaired_intellectual_development|not_specified": 1,
    "Peripheral_neuropathy|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|MCM3AP-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MCM3AP-related_disorder|not_provided|not_specified": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism": 5,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 184,
    "not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 20,
    "PCNT-related_disorder": 381,
    "PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|not_provided": 3,
    "not_provided|PCNT-related_disorder": 185,
    "not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 24,
    "PCNT-related_disorder|not_provided": 219,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 47,
    "PCNT-related_disorder|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 33,
    "Inborn_genetic_diseases|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 1,
    "not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 46,
    "not_provided|PCNT-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 11,
    "PCNT-related_disorder|not_provided|not_specified": 15,
    "PCNT-related_disorder|Inborn_genetic_diseases|not_provided": 12,
    "not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder": 8,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|PCNT-related_disorder|not_specified": 4,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_provided": 32,
    "PCNT-related_disorder|Inborn_genetic_diseases": 34,
    "Inborn_genetic_diseases|PCNT-related_disorder": 38,
    "not_specified|not_provided|PCNT-related_disorder": 5,
    "PCNT-related_disorder|Inborn_genetic_diseases|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 4,
    "not_provided|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 9,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|PCNT-related_disorder": 13,
    "PCNT-related_disorder|not_specified": 11,
    "PCNT-related_disorder|not_specified|not_provided": 20,
    "not_provided|Inborn_genetic_diseases|PCNT-related_disorder": 11,
    "not_specified|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 3,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_provided|not_specified": 2,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|not_provided": 23,
    "not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified": 8,
    "not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|PCNT-related_disorder": 3,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|Inborn_genetic_diseases": 1,
    "PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 14,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|PCNT-related_disorder|not_provided": 9,
    "not_specified|PCNT-related_disorder|Global_developmental_delay|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|not_specified": 28,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|PCNT-related_disorder|not_provided": 6,
    "not_provided|PCNT-related_disorder|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|not_provided|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 3,
    "not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_specified": 2,
    "PCNT-related_disorder|Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 4,
    "PCNT-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|PCNT-related_disorder|not_provided": 12,
    "not_provided|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 6,
    "not_provided|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder": 9,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified": 1,
    "not_provided|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified": 1,
    "Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 7,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|PCNT-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|PCNT-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|PCNT-related_disorder": 12,
    "PCNT-related_disorder|not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 15,
    "not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|Inborn_genetic_diseases": 3,
    "PCNT-related_disorder|Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 1,
    "not_provided|PCNT-related_disorder|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 2,
    "PCNT-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|PCNT-related_disorder|not_specified": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|not_provided|PCNT-related_disorder": 4,
    "not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|PCNT-related_disorder": 3,
    "PCNT-related_disorder|not_provided|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 6,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Inborn_genetic_diseases|not_provided": 2,
    "PCNT-related_disorder|not_provided|Inborn_genetic_diseases": 11,
    "PCNT-related_disorder|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 5,
    "not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder": 5,
    "not_specified|PCNT-related_disorder": 4,
    "not_specified|PCNT-related_disorder|Inborn_genetic_diseases": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_provided|Microcephaly": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|PCNT-related_disorder": 1,
    "not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Renal_cyst": 1,
    "PCNT-related_disorder|not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Intellectual_disability": 2,
    "not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Intellectual_disability": 1,
    "PCNT-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "PCNT-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 2,
    "not_provided|PCNT-related_disorder|not_specified": 6,
    "not_specified|PCNT-related_disorder|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 3,
    "not_provided|Inborn_genetic_diseases|not_specified|PCNT-related_disorder": 2,
    "Inborn_genetic_diseases|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 1,
    "not_provided|not_specified|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 2,
    "Inborn_genetic_diseases|not_provided|not_specified|PCNT-related_disorder": 1,
    "PCNT-related_disorder|not_provided|Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 1,
    "PCNT-related_disorder|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified": 1,
    "PCNT-related_disorder|Microcephaly|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided": 1,
    "not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Microcephalic_osteodysplastic_primordial_dwarfism|not_provided": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|Inborn_genetic_diseases|PCNT-related_disorder": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_specified|Inborn_genetic_diseases|not_provided|PCNT-related_disorder": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|not_provided|not_specified|PCNT-related_disorder": 2,
    "PCNT-related_disorder|not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 2,
    "Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder": 1,
    "not_provided|not_specified|PCNT-related_disorder": 3,
    "Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_provided": 1,
    "not_specified|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_provided": 1,
    "PCNT-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 1,
    "not_provided|PCNT-related_disorder|Microcephalic_osteodysplastic_primordial_dwarfism": 1,
    "not_provided|Inborn_genetic_diseases|Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder": 1,
    "PCNT-related_disorder|See_cases|not_provided": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|See_cases|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|PCNT-related_disorder": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism_type_II|PCNT-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "PCNT-related_disorder|not_specified|not_provided|Intellectual_disability|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 1,
    "Inborn_genetic_diseases|PCNT-related_disorder|not_provided|Microcephalic_osteodysplastic_primordial_dwarfism_type_II": 1,
    "Microcephalic_osteodysplastic_primordial_dwarfism|not_provided": 1,
    "DIP2A-related_disorder": 23,
    "not_provided|DIP2A-related_disorder": 1,
    "DIP2A-related_disorder|not_specified": 1,
    "DIP2A-related_disorder|not_provided": 2,
    "not_specified|DIP2A-related_disorder": 1,
    "not_provided|Familial_Candidiasis|_Recessive|not_specified": 1,
    "Familial_Candidiasis|_Recessive|not_specified|not_provided": 2,
    "Immunodeficiency_51|Familial_Candidiasis|_Recessive|not_specified|not_provided": 1,
    "IL17RA-related_disorder": 2,
    "not_provided|Immunodeficiency_51": 14,
    "Immunodeficiency_51|IL17RA-related_disorder|not_provided|Familial_Candidiasis|_Recessive": 1,
    "Immunodeficiency_51|not_specified": 28,
    "Immunodeficiency_51|IL17RA-related_disorder": 7,
    "not_specified|Immunodeficiency_51": 62,
    "IL17RA-related_disorder|Immunodeficiency_51": 2,
    "Familial_Candidiasis|_Recessive|Immunodeficiency_51": 1,
    "Immunodeficiency_51|not_provided|See_cases": 1,
    "Familial_Candidiasis|_Recessive|not_provided|Immunodeficiency_51": 4,
    "IL17RA-related_disorder|Familial_Candidiasis|_Recessive|Immunodeficiency_51": 1,
    "Immunodeficiency_51|not_provided": 11,
    "Immunodeficiency_51|not_specified|not_provided": 2,
    "not_specified|Immunodeficiency_51|not_provided": 1,
    "not_specified|not_provided|Immunodeficiency_51": 1,
    "IL17RA-related_disorder|not_provided|Immunodeficiency_51|not_specified": 1,
    "Familial_Candidiasis|_Recessive|not_specified|not_provided|Immunodeficiency_51": 4,
    "not_provided|IL17RA-related_disorder|Immunodeficiency_51|Familial_Candidiasis|_Recessive": 1,
    "not_specified|not_provided|Immunodeficiency_51|Familial_Candidiasis|_Recessive": 1,
    "Psoriasis": 1,
    "not_provided|Immunodeficiency_51|IL17RA-related_disorder": 1,
    "not_provided|Immunodeficiency_51|Familial_Candidiasis|_Recessive": 1,
    "Immunodeficiency_51|not_provided|not_specified": 1,
    "not_provided|not_specified|Immunodeficiency_51|Familial_Candidiasis|_Recessive": 1,
    "IL17RA-related_disorder|not_provided|Immunodeficiency_51": 1,
    "Familial_Candidiasis|_Recessive|not_provided": 7,
    "Familial_Candidiasis|_Recessive": 43,
    "not_provided|Familial_Candidiasis|_Recessive": 22,
    "Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome": 54,
    "Vasculitis_due_to_ADA2_deficiency": 306,
    "not_provided|Vasculitis_due_to_ADA2_deficiency": 4,
    "Vasculitis_due_to_ADA2_deficiency|ADA2-related_disorder|Sneddon_syndrome": 1,
    "Autoinflammatory_syndrome|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_specified|not_provided": 1,
    "Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome|Autoinflammatory_syndrome": 3,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency": 41,
    "not_provided|Vasculitis_due_to_ADA2_deficiency|not_specified": 2,
    "not_provided|Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome": 3,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_provided|Autoinflammatory_syndrome": 1,
    "not_provided|Vasculitis_due_to_ADA2_deficiency|ADA2-related_disorder|Autoinflammatory_syndrome": 1,
    "ADA2-related_disorder|Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome": 2,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_specified": 1,
    "not_specified|Vasculitis_due_to_ADA2_deficiency|not_provided": 1,
    "Autoinflammatory_syndrome|Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome": 3,
    "Deficiency_of_adenosine_deaminase_2": 2,
    "Vasculitis_due_to_ADA2_deficiency|not_specified|not_provided": 2,
    "Autoinflammatory_syndrome|Vasculitis_due_to_ADA2_deficiency": 8,
    "ADA2-related_disorder|Vasculitis_due_to_ADA2_deficiency": 2,
    "Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome|not_provided": 3,
    "Vasculitis_due_to_ADA2_deficiency|not_provided": 13,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_provided|Inherited_Immunodeficiency_Diseases": 1,
    "Vasculitis_due_to_ADA2_deficiency|ADA2-related_disorder": 1,
    "Sneddon_syndrome|See_cases|Vasculitis_due_to_ADA2_deficiency": 1,
    "Vasculitis_due_to_ADA2_deficiency|ADA2-related_disorder|not_provided": 1,
    "Vasculitis_due_to_ADA2_deficiency|not_provided|ADA2-related_disorder|Sneddon_syndrome": 1,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome": 2,
    "not_specified|Vasculitis_due_to_ADA2_deficiency|Behcet_disease|not_provided|ADA2-related_disorder|Autoinflammatory_syndrome": 1,
    "Sneddon_syndrome": 2,
    "not_specified|not_provided|Vasculitis_due_to_ADA2_deficiency": 1,
    "not_provided|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency": 2,
    "ADA2-related_disorder|Vasculitis_due_to_ADA2_deficiency|not_provided|Sneddon_syndrome": 1,
    "ADA2-related_disorder|Behcet_disease|not_provided|Autoinflammatory_syndrome|Vasculitis_due_to_ADA2_deficiency|not_specified": 1,
    "Deficiency_of_ADA2": 1,
    "Vasculitis_due_to_ADA2_deficiency|not_provided|Sneddon_syndrome": 2,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_provided": 3,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|Behcet_disease": 1,
    "Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome|ADA2-related_disorder": 1,
    "Autoinflammatory_syndrome|Vasculitis_due_to_ADA2_deficiency|not_provided": 1,
    "Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome|Sneddon_syndrome": 1,
    "Autoinflammatory_syndrome|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency": 2,
    "Polyarteritis_nodosa": 1,
    "ADA2-related_disorder|Vasculitis_due_to_ADA2_deficiency|not_provided|not_specified": 1,
    "Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome|not_provided": 1,
    "ADA2-related_disorder|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome|Inherited_Immunodeficiency_Diseases|not_provided": 1,
    "not_provided|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome": 1,
    "Vasculitis_due_to_ADA2_deficiency|Autoinflammatory_syndrome": 2,
    "Vasculitis_due_to_ADA2_deficiency|not_provided|Autoinflammatory_syndrome": 2,
    "Autoinflammatory_syndrome|not_provided|Vasculitis_due_to_ADA2_deficiency": 1,
    "Autoinflammatory_syndrome|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_provided": 2,
    "Deficiency_of_ADA2|Vasculitis_due_to_ADA2_deficiency|Sneddon_syndrome": 1,
    "not_provided|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|Behcet_disease|Autoinflammatory_syndrome": 1,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|not_provided|Splenomegaly": 1,
    "Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|ADA2-related_disorder|not_provided": 1,
    "Autoinflammatory_syndrome|Sneddon_syndrome|Vasculitis_due_to_ADA2_deficiency|ADA2-related_disorder|not_provided": 1,
    "Vasculitis_due_to_ADA2_deficiency|not_specified": 1,
    "ADA2-related_disorder|not_specified": 1,
    "CECR2-related_neurodevelopmental_disorder": 5,
    "CECR2-related_neurodevelopmental_disorder|See_cases": 1,
    "Autosomal_recessive_cutis_laxa_type_2C|not_provided": 1,
    "Autosomal_recessive_cutis_laxa_type_2C": 2,
    "Autosomal_recessive_cutis_laxa_type_2C|Cutis_laxa|not_provided": 1,
    "ATP6V1E1-related_disorder|not_provided": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)": 92,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|not_provided": 5,
    "not_provided|Peroxisome_biogenesis_disorder_7A_(Zellweger)": 16,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 319,
    "not_provided|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 16,
    "PEX26-related_disorder": 3,
    "Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder_7A_(Zellweger)": 12,
    "not_provided|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided|PEX26-related_disorder": 1,
    "not_provided|PEX26-related_disorder|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 2,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided": 16,
    "Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder_7A_(Zellweger)|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 13,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|PEX26-related_disorder|not_provided": 2,
    "PEX26-related_disorder|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided": 3,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 2,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|not_provided|Peroxisome_biogenesis_disorder_7B|not_specified": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided|not_specified": 2,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 2,
    "Peroxisome_biogenesis_disorder_7B": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|PEX26-related_disorder": 4,
    "not_specified|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 2,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_7B": 1,
    "Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Inborn_genetic_diseases": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_specified": 1,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided|PEX26-related_disorder": 1,
    "not_specified|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided": 1,
    "PEX26-related_disorder|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 3,
    "PEX26-related_disorder|not_specified|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided": 2,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_specified|not_provided|Peroxisome_biogenesis_disorder_1A_(Zellweger)": 1,
    "Heimler_syndrome_1|not_specified|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided|Optic_atrophy": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|Inborn_genetic_diseases|not_provided": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_7B|not_provided": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided|Peroxisome_biogenesis_disorder": 1,
    "Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder_7A_(Zellweger)|not_provided": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_specified|PEX26-related_disorder": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|PEX26-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|Inborn_genetic_diseases": 1,
    "Retinal_dystrophy|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 1,
    "PEX26-related_disorder|Inborn_genetic_diseases|not_provided|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 1,
    "Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B|not_provided": 2,
    "Peroxisome_biogenesis_disorder|Peroxisome_biogenesis_disorder_7B|Peroxisome_biogenesis_disorder_7A_(Zellweger)|PEX26-related_disorder|not_provided": 1,
    "not_specified|PEX26-related_disorder|Peroxisome_biogenesis_disorder_7A_(Zellweger)|Peroxisome_biogenesis_disorder_7B": 1,
    "not_specified|Peroxisome_biogenesis_disorder_7A_(Zellweger)|not_provided": 1,
    "not_specified|TUBA8-related_disorder": 1,
    "Polymicrogyria_with_optic_nerve_hypoplasia": 1,
    "Polymicrogyria_with_optic_nerve_hypoplasia|not_provided": 3,
    "Macrothrombocytopenia|_isolated|_2|_autosomal_dominant": 2,
    "not_provided|TUBA8-related_disorder|not_specified": 3,
    "not_provided|Macrothrombocytopenia|_isolated|_2|_autosomal_dominant": 1,
    "not_provided|TUBA8-related_disorder": 2,
    "TUBA8-related_disorder": 1,
    "TUBA8-related_disorder|not_provided": 2,
    "Polymicrogyria_with_optic_nerve_hypoplasia|not_provided|Macrothrombocytopenia|_isolated|_2|_autosomal_dominant": 1,
    "TUBA8-related_disorder|not_specified|not_provided": 2,
    "TUBA8-related_disorder|not_provided|Macrothrombocytopenia|_isolated|_2|_autosomal_dominant": 1,
    "not_provided|Polymicrogyria_with_optic_nerve_hypoplasia": 1,
    "not_specified|not_provided|Polymicrogyria_with_optic_nerve_hypoplasia|Macrothrombocytopenia|_isolated|_2|_autosomal_dominant": 1,
    "TUBA8-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|Polymicrogyria_with_optic_nerve_hypoplasia": 1,
    "not_provided|USP18-related_disorder": 1,
    "Pseudo-TORCH_syndrome_2": 5,
    "Inborn_genetic_diseases|Pseudo-TORCH_syndrome_2": 1,
    "Proline_dehydrogenase_deficiency|not_provided": 19,
    "Proline_dehydrogenase_deficiency": 184,
    "Schizophrenia_4|Proline_dehydrogenase_deficiency": 74,
    "Proline_dehydrogenase_deficiency|Schizophrenia_4": 42,
    "Schizophrenia_4|Proline_dehydrogenase_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Proline_dehydrogenase_deficiency": 12,
    "Proline_dehydrogenase_deficiency|not_provided|Schizophrenia_4|Inborn_genetic_diseases": 1,
    "Proline_dehydrogenase_deficiency|Inborn_genetic_diseases": 2,
    "Proline_dehydrogenase_deficiency|Schizophrenia_4|Inborn_genetic_diseases": 4,
    "not_provided|Proline_dehydrogenase_deficiency|Schizophrenia_4": 5,
    "not_specified|Schizophrenia_4|Proline_dehydrogenase_deficiency": 2,
    "Proline_dehydrogenase_deficiency|Schizophrenia_4|not_provided": 6,
    "Inborn_genetic_diseases|Proline_dehydrogenase_deficiency|Schizophrenia_4|not_provided": 1,
    "Inborn_genetic_diseases|Schizophrenia_4|Proline_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "not_specified|Proline_dehydrogenase_deficiency|Schizophrenia_4": 1,
    "Proline_dehydrogenase_deficiency|not_provided|Schizophrenia_4": 2,
    "Inborn_genetic_diseases|Proline_dehydrogenase_deficiency": 1,
    "Proline_dehydrogenase_deficiency|Schizophrenia_4|not_specified": 1,
    "Schizophrenia_4": 1,
    "not_specified|Proline_dehydrogenase_deficiency|Schizophrenia_4|not_provided": 1,
    "Proline_dehydrogenase_deficiency|not_specified": 1,
    "not_provided|Schizophrenia_4|Proline_dehydrogenase_deficiency": 1,
    "Schizophrenia_4|Proline_dehydrogenase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Proline_dehydrogenase_deficiency|not_specified": 1,
    "Proline_dehydrogenase_deficiency|not_specified|not_provided": 1,
    "Schizophrenia_4|Proline_dehydrogenase_deficiency|not_specified": 1,
    "2-hydroxyglutaric_aciduria": 1,
    "SLC25A1-related_disorder|not_specified|not_provided": 1,
    "2-hydroxyglutaric_aciduria|SLC25A1-related_disorder": 2,
    "D|L-2-hydroxyglutaric_aciduria|not_provided": 4,
    "D|L-2-hydroxyglutaric_aciduria|2-hydroxyglutaric_aciduria|not_provided": 2,
    "Myasthenic_syndrome|_congenital|_23|_presynaptic|2-hydroxyglutaric_aciduria": 1,
    "not_provided|SLC25A1-related_disorder|Inborn_genetic_diseases": 1,
    "SLC25A1-related_disorder": 4,
    "Myasthenic_syndrome|_congenital|_23|_presynaptic": 6,
    "2-hydroxyglutaric_aciduria|not_provided": 1,
    "not_provided|2-hydroxyglutaric_aciduria": 1,
    "not_provided|SLC25A1-related_disorder": 1,
    "not_provided|not_specified|SLC25A1-related_disorder": 1,
    "SLC25A1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "SLC25A1-related_disorder|not_specified": 1,
    "CLTCL1-related_disorder": 17,
    "CLTCL1-related_disorder|not_provided": 3,
    "not_provided|CLTCL1-related_disorder": 5,
    "not_specified|CLTCL1-related_disorder": 1,
    "not_provided|HIRA-related_disorder": 9,
    "HIRA-related_disorder": 12,
    "HIRA-related_disorder|not_provided": 5,
    "UFD1-related_disorder": 1,
    "UFD1-related_disorder|not_provided": 1,
    "Meier-Gorlin_syndrome_7": 9,
    "CDC45-related_disorder|not_specified|not_provided": 1,
    "Meier-Gorlin_syndrome_7|not_provided": 3,
    "not_provided|CDC45-related_disorder": 2,
    "CDC45-related_disorder|not_provided": 2,
    "not_specified|CDC45-related_disorder|not_provided": 1,
    "not_provided|Androgen_resistance_syndrome|CDC45-related_disorder": 1,
    "not_provided|Meier-Gorlin_syndrome_7": 4,
    "Meier-Gorlin_syndrome_7|Inborn_genetic_diseases|not_provided": 1,
    "CDC45-related_disorder": 1,
    "CLDN5-related_neurodevelopmental_disorder": 2,
    "Inborn_genetic_diseases|CLDN5-related_neurodevelopmental_disorder": 1,
    "CLDN5_deficiency": 1,
    "CLDN5-associated_neurodevelopmental_disorder": 1,
    "Macrothrombocytopenia|Abnormal_bleeding": 1,
    "Bernard-Soulier_syndrome|_type_B": 1,
    "GP1BB-related_disorder": 8,
    "Mild_macrothrombocytopenia|Bernard_Soulier_syndrome": 1,
    "Thrombocytopenia|not_provided|Bernard_Soulier_syndrome|Macrothrombocytopenia": 1,
    "GP1BB-related_disorder|not_specified|not_provided": 1,
    "Macrothrombocytopenia|Bernard-Soulier_syndrome|_type_B|Bernard_Soulier_syndrome|Increased_mean_platelet_volume|Thrombocytopenia": 1,
    "Bernard_Soulier_syndrome|Thrombocytopenia": 1,
    "Thrombocytopenia|not_provided|Bernard_Soulier_syndrome": 1,
    "GP1BB-related_disorder|not_provided|not_specified": 1,
    "Bernard_Soulier_syndrome|MACROTHROMBOCYTOPENIA|_FAMILIAL|_BERNARD-SOULIER_TYPE": 1,
    "Bernard-Soulier_syndrome|_type_B|GP1BB-related_disorder": 1,
    "Bernard_Soulier_syndrome|not_provided|GP1BB-related_disorder|not_specified": 1,
    "MACROTHROMBOCYTOPENIA|_FAMILIAL|_BERNARD-SOULIER_TYPE": 1,
    "GP1BB-related_disorder|not_specified": 1,
    "not_provided|GP1BB-related_disorder|Bernard_Soulier_syndrome": 1,
    "Thrombocytopenia|Bernard_Soulier_syndrome|not_specified|Macrothrombocytopenia": 1,
    "Mild_macrothrombocytopenia": 2,
    "not_provided|GP1BB-related_disorder": 1,
    "DiGeorge_syndrome": 465,
    "TBX1-related_disorder": 17,
    "not_provided|not_specified|DiGeorge_syndrome": 1,
    "not_provided|DiGeorge_syndrome": 17,
    "DiGeorge_syndrome|Cardiovascular_phenotype": 59,
    "Velocardiofacial_syndrome|DiGeorge_syndrome": 2,
    "DiGeorge_syndrome|not_provided": 22,
    "Cardiovascular_phenotype|DiGeorge_syndrome": 61,
    "Cardiovascular_phenotype|not_provided|DiGeorge_syndrome": 7,
    "DiGeorge_syndrome|not_provided|Cardiovascular_phenotype": 7,
    "Velocardiofacial_syndrome|Conotruncal_heart_malformations|DiGeorge_syndrome|Tetralogy_of_Fallot": 1,
    "DiGeorge_syndrome|Cardiovascular_phenotype|not_provided": 3,
    "TBX1-related_disorder|not_provided|DiGeorge_syndrome|Velocardiofacial_syndrome|Tetralogy_of_Fallot|Conotruncal_heart_malformations": 1,
    "DiGeorge_syndrome|Conotruncal_heart_malformations|Velocardiofacial_syndrome|Tetralogy_of_Fallot": 3,
    "Cardiovascular_phenotype|DiGeorge_syndrome|not_specified": 3,
    "DiGeorge_syndrome|Velocardiofacial_syndrome": 1,
    "DiGeorge_syndrome|TBX1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|DiGeorge_syndrome": 2,
    "DiGeorge_syndrome|not_specified": 6,
    "DiGeorge_syndrome|not_specified|Cardiovascular_phenotype": 2,
    "TBX1-related_disorder|not_provided|DiGeorge_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|DiGeorge_syndrome|not_provided": 5,
    "not_provided|DiGeorge_syndrome|Cardiovascular_phenotype": 4,
    "not_provided|TBX1-related_disorder|DiGeorge_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "DiGeorge_syndrome|Cardiovascular_phenotype|TBX1-related_disorder": 2,
    "TBX1-related_disorder|not_specified|Cardiovascular_phenotype|not_provided|DiGeorge_syndrome": 2,
    "TBX1-related_disorder|Cardiovascular_phenotype|DiGeorge_syndrome": 2,
    "TBX1-related_disorder|Cardiovascular_phenotype|not_provided|DiGeorge_syndrome": 1,
    "Cardiovascular_phenotype|DiGeorge_syndrome|Conotruncal_heart_malformations|Velocardiofacial_syndrome|Tetralogy_of_Fallot": 1,
    "TBX1-related_disorder|DiGeorge_syndrome": 5,
    "DiGeorge_syndrome|Tetralogy_of_Fallot": 1,
    "Tetralogy_of_Fallot|DiGeorge_syndrome|Velocardiofacial_syndrome": 1,
    "DiGeorge_syndrome|TBX1-related_disorder": 4,
    "not_provided|DiGeorge_syndrome|TBX1-related_disorder": 4,
    "not_specified|not_provided|DiGeorge_syndrome|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_specified|TBX1-related_disorder|DiGeorge_syndrome": 1,
    "Conotruncal_anomaly_face_syndrome": 2,
    "not_provided|DiGeorge_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Velocardiofacial_syndrome": 3,
    "Velocardiofacial_syndrome|DiGeorge_syndrome|not_provided": 1,
    "DiGeorge_syndrome|TBX1-related_disorder|Cardiovascular_phenotype": 1,
    "Tetralogy_of_Fallot|Velocardiofacial_syndrome|DiGeorge_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|DiGeorge_syndrome": 4,
    "not_specified|DiGeorge_syndrome": 1,
    "not_specified|not_provided|DiGeorge_syndrome": 2,
    "not_provided|Conotruncal_heart_malformations|Velocardiofacial_syndrome|DiGeorge_syndrome|Tetralogy_of_Fallot": 2,
    "Cardiovascular_phenotype|not_provided|DiGeorge_syndrome|TBX1-related_disorder": 1,
    "TBX1-related_disorder|DiGeorge_syndrome|Cardiovascular_phenotype": 2,
    "DiGeorge_syndrome|Velocardiofacial_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot|TBX1-related_disorder": 1,
    "DiGeorge_syndrome|Velocardiofacial_syndrome|Tetralogy_of_Fallot": 1,
    "Velocardiofacial_syndrome|DiGeorge_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot": 1,
    "DiGeorge_syndrome|not_provided|Velocardiofacial_syndrome|Tetralogy_of_Fallot|Conotruncal_heart_malformations": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|DiGeorge_syndrome": 1,
    "Cardiovascular_phenotype|TBX1-related_disorder|not_provided": 2,
    "Cardiovascular_phenotype|DiGeorge_syndrome|TBX1-related_disorder": 2,
    "TBX1-related_disorder|Cardiovascular_phenotype": 1,
    "DiGeorge_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Velocardiofacial_syndrome": 1,
    "Conotruncal_heart_malformations|Velocardiofacial_syndrome|DiGeorge_syndrome|Tetralogy_of_Fallot": 1,
    "Cardiovascular_phenotype|not_provided|DiGeorge_syndrome|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Velocardiofacial_syndrome|not_specified": 1,
    "not_provided|DiGeorge_syndrome|TBX1-related_disorder|Cardiovascular_phenotype": 1,
    "Conotruncal_heart_malformations|Tetralogy_of_Fallot|Velocardiofacial_syndrome|DiGeorge_syndrome|not_provided": 1,
    "DiGeorge_syndrome|not_specified|Cardiovascular_phenotype|TBX1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|TBX1-related_disorder|DiGeorge_syndrome": 1,
    "DiGeorge_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Velocardiofacial_syndrome|not_provided": 1,
    "not_provided|DiGeorge_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot|Velocardiofacial_syndrome|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|DiGeorge_syndrome": 1,
    "TBX1-related_disorder|DiGeorge_syndrome|not_specified": 1,
    "Cardiovascular_phenotype|DiGeorge_syndrome|not_specified|TBX1-related_disorder|not_provided": 1,
    "TBX1-related_disorder|not_provided|Cardiovascular_phenotype|DiGeorge_syndrome": 1,
    "Cardiovascular_phenotype|DiGeorge_syndrome|not_provided|not_specified": 1,
    "DiGeorge_syndrome|Cardiovascular_phenotype|Velocardiofacial_syndrome|Conotruncal_heart_malformations|Tetralogy_of_Fallot": 1,
    "Cardiovascular_phenotype|DiGeorge_syndrome|Tetralogy_of_Fallot|Conotruncal_heart_malformations|Velocardiofacial_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|TBX1-related_disorder|DiGeorge_syndrome": 1,
    "DiGeorge_syndrome|Tetralogy_of_Fallot|not_provided": 1,
    "TBX1-related_disorder|Cardiovascular_phenotype|DiGeorge_syndrome|not_provided": 1,
    "not_specified|DiGeorge_syndrome|not_provided|Cardiovascular_phenotype": 1,
    "DiGeorge_syndrome|not_provided|TBX1-related_disorder|Cardiovascular_phenotype": 1,
    "DiGeorge_syndrome|Hypoplastic_left_heart_syndrome|Cardiovascular_phenotype": 1,
    "TBX1-related_disorder|not_provided": 1,
    "Velocardiofacial_syndrome|DiGeorge_syndrome|Tetralogy_of_Fallot|Conotruncal_heart_malformations": 1,
    "GNB1L-related_disorder": 10,
    "not_provided|GNB1L-related_disorder": 3,
    "GNB1L-related_disorder|not_specified": 1,
    "TXNRD2-related_disorder": 6,
    "Primary_dilated_cardiomyopathy|not_provided|TXNRD2-related_disorder|Cardiovascular_phenotype": 3,
    "TXNRD2-related_disorder|not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_specified": 2,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|TXNRD2-related_disorder": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided|Glucocorticoid_deficiency_5": 1,
    "Glucocorticoid_deficiency_5|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 3,
    "Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 2,
    "Glucocorticoid_deficiency_5|Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|TXNRD2-related_disorder|Primary_dilated_cardiomyopathy|not_specified|not_provided": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "TXNRD2-related_disorder|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 2,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|not_provided": 7,
    "Glucocorticoid_deficiency_5": 4,
    "not_specified|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 2,
    "Glucocorticoid_deficiency_5|not_specified|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|TXNRD2-related_disorder": 2,
    "Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|Cardiovascular_phenotype": 4,
    "Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy|TXNRD2-related_disorder": 1,
    "not_provided|Glucocorticoid_deficiency_5": 1,
    "not_provided|TXNRD2-related_disorder": 2,
    "Cardiovascular_phenotype|TXNRD2-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "TXNRD2-related_disorder|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|not_specified": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "TXNRD2-related_disorder|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided|Glucocorticoid_deficiency_5|not_specified": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|not_specified": 1,
    "not_provided|TXNRD2-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|not_provided": 1,
    "not_provided|Glucocorticoid_deficiency_5|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Glucocorticoid_deficiency_5|Primary_dilated_cardiomyopathy": 1,
    "Primary_familial_hypertrophic_cardiomyopathy|Primary_dilated_cardiomyopathy": 3,
    "Glucocorticoid_deficiency_5|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Glucocorticoid_deficiency_5": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy": 1,
    "TXNRD2-related_disorder|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy": 1,
    "Glucocorticoid_deficiency_5|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5": 2,
    "not_provided|not_specified|Glucocorticoid_deficiency_5|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|TXNRD2-related_disorder|Cardiovascular_phenotype": 1,
    "Primary_dilated_cardiomyopathy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|TXNRD2-related_disorder|not_provided|Cardiomyopathy|Primary_dilated_cardiomyopathy": 1,
    "not_specified|not_provided|Glucocorticoid_deficiency_5|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|Primary_dilated_cardiomyopathy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Glucocorticoid_deficiency_5|TXNRD2-associated_Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|TXNRD2-related_disorder|Primary_dilated_cardiomyopathy|Glucocorticoid_deficiency_5|not_specified|not_provided": 1,
    "TXNRD2-related_disorder|Cardiovascular_phenotype|not_provided|Primary_dilated_cardiomyopathy": 1,
    "Glucocorticoid_deficiency_5|not_provided|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Glucocorticoid_deficiency_5|Primary_dilated_cardiomyopathy": 1,
    "Schizophrenia|Panic_disorder_1": 1,
    "COMT-related_disorder": 4,
    "Tramadol_response|not_specified|not_provided": 1,
    "Schizophrenia|_susceptibility_to|Tramadol_response|22q11.2_deletion_syndrome": 1,
    "not_provided|COMT-related_disorder": 2,
    "not_provided|methamphetamine_use_disorder|Tramadol_response|not_specified": 1,
    "Panic_disorder_1|Schizophrenia": 1,
    "not_specified|not_provided|Schizophrenia|CATECHOL-O-METHYLTRANSFERASE_POLYMORPHISM|Tramadol_response": 1,
    "Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome": 15,
    "TANGO2-related_disorder": 5,
    "Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|not_provided": 5,
    "TANGO2-related_disorder|not_provided": 6,
    "Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|TANGO2-related_disorder|not_provided": 1,
    "TANGO2-related_disorder|Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|not_provided": 1,
    "not_provided|Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome": 6,
    "Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|Acute_rhabdomyolysis|Seizure|Episodic_flaccid_weakness|Intellectual_disability|Cardiac_arrhythmia": 1,
    "not_provided|TANGO2-related_disorder": 5,
    "TANGO2-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Metabolic_crises_with_rhabdomyolysis|_cardiac_arrhythmias|_and_neurodegeneration|Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome": 1,
    "not_provided|Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|Acute_rhabdomyolysis|Seizure|Episodic_flaccid_weakness|Intellectual_disability|Cardiac_arrhythmia": 1,
    "Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|not_provided|TANGO2-related_disorder|Episodic_flaccid_weakness|Seizure|Intellectual_disability|Cardiac_arrhythmia|Acute_rhabdomyolysis|Abnormality_of_metabolism/homeostasis": 1,
    "Recurrent_metabolic_encephalomyopathic_crises-rhabdomyolysis-cardiac_arrhythmia-intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|DGCR8-related_disorder": 1,
    "DGCR8-related_disorder": 4,
    "RTN4R-related_disorder": 7,
    "Schizophrenia|_susceptibility_to": 2,
    "RTN4R-related_disorder|not_specified": 1,
    "Van_den_Ende-Gupta_syndrome": 21,
    "Van_den_Ende-Gupta_syndrome|not_provided": 1,
    "Van_den_Ende-Gupta_syndrome|not_specified|not_provided": 1,
    "not_provided|not_specified|Van_den_Ende-Gupta_syndrome": 1,
    "Van_den_Ende-Gupta_syndrome|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Van_den_Ende-Gupta_syndrome": 1,
    "SCARF2-related_disorder": 2,
    "SCARF2-related_disorder|not_provided": 1,
    "not_provided|SCARF2-related_disorder": 1,
    "not_provided|Van_den_Ende-Gupta_syndrome": 2,
    "not_provided|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis": 3,
    "Spastic_paraplegia_84|_autosomal_recessive|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_provided": 1,
    "PI4KA-related_disorder": 35,
    "Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis": 28,
    "Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_provided": 11,
    "not_provided|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_specified": 2,
    "Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_specified|not_provided": 2,
    "Spastic_paraplegia_84|_autosomal_recessive": 6,
    "Spastic_paraplegia_84|_autosomal_recessive|Gastrointestinal_defects_and_immunodeficiency_syndrome_2|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_provided": 1,
    "Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_provided|not_specified": 3,
    "not_specified|PI4KA-related_disorder|not_provided": 1,
    "not_provided|not_specified|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis": 2,
    "Gastrointestinal_defects_and_immunodeficiency_syndrome_2": 2,
    "not_provided|PI4KA-related_disorder|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis": 2,
    "not_provided|not_specified|Spastic_paraplegia_84|_autosomal_recessive": 1,
    "PI4KA-related_disorder|not_provided": 4,
    "not_provided|PI4KA-related_disorder": 4,
    "Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|Gastrointestinal_defects_and_immunodeficiency_syndrome_2|Spastic_paraplegia_84|_autosomal_recessive": 1,
    "SERPIND1-related_disorder": 8,
    "not_provided|Heparin_cofactor_II_deficiency": 2,
    "SERPIND1-related_disorder|not_provided": 2,
    "Heparin_cofactor_II_deficiency|SERPIND1-related_disorder": 1,
    "not_provided|SERPIND1-related_disorder": 1,
    "not_specified|Heparin_cofactor_II_deficiency": 1,
    "Thrombotic_stroke|SERPIND1-related_disorder": 1,
    "not_provided|Gastrointestinal_defects_and_immunodeficiency_syndrome_2|Spastic_paraplegia_84|_autosomal_recessive|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|Phenylketonuria|PI4KA-related_disorder": 1,
    "not_specified|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|not_provided": 1,
    "not_specified|not_provided|Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis": 1,
    "Polymicrogyria|_perisylvian|_with_cerebellar_hypoplasia_and_arthrogryposis|Spastic_paraplegia_84|_autosomal_recessive": 1,
    "CEDNIK_syndrome": 99,
    "not_provided|CEDNIK_syndrome": 18,
    "CEDNIK_syndrome|not_provided": 22,
    "not_provided|not_specified|CEDNIK_syndrome": 4,
    "SNAP29-related_disorder": 3,
    "not_provided|CEDNIK_syndrome|Hypomyelinating_leukodystrophy_2": 1,
    "not_provided|SNAP29-related_disorder|CEDNIK_syndrome": 1,
    "CEDNIK_syndrome|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|CEDNIK_syndrome": 2,
    "not_specified|not_provided|CEDNIK_syndrome": 1,
    "CEDNIK_syndrome|SNAP29-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|CEDNIK_syndrome|Hypomyelinating_leukodystrophy_2": 1,
    "SNAP29-related_disorder|not_provided": 1,
    "CEDNIK_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CEDNIK_syndrome|not_provided": 1,
    "not_provided|SNAP29-related_disorder": 1,
    "not_provided|not_specified|SNAP29-related_disorder": 1,
    "not_specified|CEDNIK_syndrome": 1,
    "CRKL-related_disorder|not_provided": 1,
    "not_provided|CRKL-related_disorder": 2,
    "CRKL-related_disorder": 2,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2": 5,
    "Noonan_syndrome|Noonan_syndrome_2|Noonan_syndrome_10|not_provided|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "LZTR1-related_disorder|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided": 1,
    "Schwannomatosis": 7,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 6,
    "LZTR1-related_schwannomatosis": 46,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|LZTR1-related_schwannomatosis|RASopathy|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Pigmentary_skin_disorders|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|LZTR1-related_schwannomatosis": 8,
    "LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 11,
    "LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|Noonan_syndrome_2|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 5,
    "not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|LZTR1-related_schwannomatosis": 14,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 4,
    "LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 13,
    "not_specified|not_provided|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|not_provided|LZTR1-related_schwannomatosis": 1,
    "Short_stature|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 8,
    "LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 6,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Noonan_syndrome_2": 9,
    "Familial_multiple_meningioma": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided": 24,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder": 4,
    "LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 15,
    "not_provided|LZTR1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis": 2,
    "Noonan_syndrome_2|not_provided": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|See_cases": 1,
    "LZTR1-related_disorder|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 4,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 8,
    "Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "not_provided|Noonan_syndrome_2|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_provided": 12,
    "LZTR1-related_schwannomatosis|not_provided": 14,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis": 5,
    "LZTR1-related_disorder|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|LZTR1-related_schwannomatosis": 12,
    "Noonan_syndrome_10": 16,
    "LZTR1-related_disorder": 13,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 4,
    "not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 5,
    "LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|not_provided|not_specified": 1,
    "LZTR1-related_disorder|not_provided|RASopathy|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 1,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Developmental_disorder|Schwannomatosis|not_provided": 1,
    "not_provided|RASopathy|Noonan_syndrome_10": 1,
    "Noonan_syndrome_10|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 3,
    "not_provided|LZTR1-related_disorder": 4,
    "Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "not_provided|Noonan_syndrome_2": 2,
    "Schwannomatosis|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|LZTR1-related_schwannomatosis": 1,
    "not_provided|Pediatric_high-grade_glioma": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10": 6,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis": 14,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 9,
    "LZTR1-related_schwannomatosis|Schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 15,
    "LZTR1-related_schwannomatosis|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|LZTR1-related_schwannomatosis|RASopathy": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_2|Noonan_syndrome_10": 2,
    "LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Schwannomatosis|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided": 1,
    "not_provided|not_specified|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "Schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis": 1,
    "not_specified|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 3,
    "Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Schwannomatosis": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|LZTR1-related_schwannomatosis|LZTR1-related_disorder|not_provided": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|LZTR1-related_schwannomatosis": 1,
    "Primary_dilated_cardiomyopathy|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Schwannomatosis": 2,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10": 3,
    "not_provided|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|not_provided": 1,
    "LZTR1-related_schwannomatosis|LZTR1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder|not_provided": 1,
    "Noonan_syndrome|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_provided": 1,
    "Noonan_syndrome_2|Noonan_syndrome_10|not_provided|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2": 1,
    "not_provided|Noonan_syndrome_2|Noonan_syndrome_10": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_provided": 2,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|LZTR1-related_schwannomatosis": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|LZTR1-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|Noonan_syndrome_10|not_provided|Noonan_syndrome|LZTR1-related_schwannomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10": 3,
    "Schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided": 1,
    "Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Schwannomatosis|Emery-Dreifuss_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_provided|LZTR1-related_disorder": 1,
    "not_provided|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 2,
    "not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "LZTR1-related_schwannomatosis|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|LZTR1-related_disorder|Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "LZTR1-related_disorder|not_provided": 6,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|LZTR1-related_disorder|not_provided": 1,
    "not_specified|LZTR1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|not_provided": 1,
    "not_provided|LZTR1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_provided": 2,
    "LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 5,
    "LZTR1-related_disorder|LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "LZTR1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 7,
    "not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|not_provided": 3,
    "Noonan_syndrome_2|not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 6,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|not_provided": 2,
    "not_specified|LZTR1-related_disorder|not_provided": 1,
    "not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "RASopathy|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis": 13,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|not_provided": 8,
    "LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "not_provided|LZTR1-related_schwannomatosis|Schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_10|not_provided": 4,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|LZTR1-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided|not_specified": 1,
    "LZTR1-related_schwannomatosis|not_provided|Noonan_syndrome_2|Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "Hypertrophic_cardiomyopathy_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 1,
    "not_provided|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder|Noonan_syndrome|Noonan_syndrome_1|Fetal_cystic_hygroma|RASopathy": 1,
    "not_provided|Autism_spectrum_disorder|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_provided|Schwannomatosis": 1,
    "LZTR1-related_disorder|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|RASopathy": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Noonan_syndrome_and_Noonan-related_syndrome|LZTR1-related_disorder|RASopathy|Noonan_syndrome_1": 1,
    "Noonan_syndrome_10|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|Noonan_syndrome_2|not_provided|RASopathy": 1,
    "RASopathy|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_1": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|LZTR1-related_disorder": 1,
    "LZTR1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|LZTR1-related_schwannomatosis": 1,
    "not_provided|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Noonan_syndrome_10|Noonan_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided|LZTR1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_disorder|not_specified": 1,
    "LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis": 6,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "LZTR1-related_schwannomatosis|not_specified|Noonan_syndrome_10|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2": 1,
    "Noonan_syndrome_2|Congenital_diaphragmatic_hernia|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis": 1,
    "LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|LZTR1-related_disorder": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|Noonan_syndrome_10": 1,
    "LZTR1-related_schwannomatosis|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Noonan_syndrome_2|not_provided|RASopathy|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis": 1,
    "not_provided|LZTR1-related_schwannomatosis|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Schwannomatosis": 1,
    "not_specified|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_2|not_provided": 1,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder": 2,
    "Short_stature|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Noonan_syndrome_2|Noonan_syndrome_and_Noonan-related_syndrome|Schwannomatosis|not_provided|RASopathy|See_cases": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_specified": 3,
    "Noonan_syndrome_10|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Bladder_exstrophy|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_provided|RASopathy": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|RASopathy|not_provided": 1,
    "LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 3,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder": 1,
    "LZTR1-related_schwannomatosis|not_provided|not_specified|Intellectual_disability|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_2|Noonan_syndrome_10|not_provided|not_specified|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_10": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|not_specified|RASopathy|not_provided|Noonan_syndrome_2|Noonan_syndrome_and_Noonan-related_syndrome|LZTR1-related_schwannomatosis|Non-immune_hydrops_fetalis|LZTR1-related_disorder": 1,
    "RASopathy|not_provided|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_10": 1,
    "not_provided|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|Noonan_syndrome_10": 1,
    "Noonan_syndrome_2|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|Noonan_syndrome_2|not_provided|Noonan_syndrome_1|LZTR1-related_schwannomatosis": 1,
    "LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|not_provided": 2,
    "LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2": 1,
    "not_specified|RASopathy|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis": 1,
    "Schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Noonan_syndrome": 1,
    "Noonan_syndrome_10|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2": 1,
    "not_provided|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2": 1,
    "not_specified|not_provided|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "Noonan_syndrome_2|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_disorder|not_provided": 1,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Schwannomatosis|not_provided": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "Noonan_syndrome_2|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2|not_specified": 1,
    "not_provided|Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Noonan_syndrome|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "not_provided|LZTR1-related_schwannomatosis|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|LZTR1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|not_provided|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_provided": 3,
    "not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_10": 1,
    "Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|LZTR1-related_schwannomatosis|not_provided": 1,
    "not_provided|Noonan_syndrome_2|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 2,
    "not_provided|LZTR1-related_schwannomatosis|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 1,
    "LZTR1-related_schwannomatosis|LZTR1-related_disorder": 1,
    "not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Diffuse_midline_glioma|_H3_K27-altered|Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided": 2,
    "Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_provided|Noonan_syndrome_10": 1,
    "not_provided|Noonan_syndrome_2|LZTR1-related_disorder|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|RASopathy|not_provided": 2,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|LZTR1-related_disorder": 1,
    "Noonan_syndrome_10|not_specified|RASopathy|LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|Noonan_syndrome_2|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|not_specified|RASopathy|not_provided": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Schwannomatosis|not_provided": 1,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Schwannomatosis|not_provided|LZTR1-related_schwannomatosis": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_10": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|LZTR1-related_schwannomatosis": 1,
    "not_specified|LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|Noonan_syndrome_10|LZTR1-related_schwannomatosis": 1,
    "Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2": 2,
    "not_provided|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10": 1,
    "not_provided|See_cases|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|LZTR1-related_disorder|not_provided": 1,
    "LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided": 1,
    "LZTR1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|not_provided": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome_2|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2|RASopathy|Noonan_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis": 1,
    "Noonan_syndrome_10|not_specified|LZTR1-related_schwannomatosis|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_2": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified": 1,
    "Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_provided|Noonan_syndrome_2": 1,
    "not_provided|not_specified|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|LZTR1-related_disorder": 1,
    "not_provided|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Hereditary_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|not_provided": 1,
    "Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Schwannomatosis|LZTR1-related_disorder|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|not_provided": 1,
    "not_specified|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided": 1,
    "Noonan_syndrome_10|LZTR1-related_schwannomatosis|Noonan_syndrome_2|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "LZTR1-related_schwannomatosis|not_provided|Bladder_exstrophy|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "LZTR1-related_disorder|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_10|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "LZTR1-related_disorder|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided": 1,
    "LZTR1-related_schwannomatosis|not_specified|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|RASopathy|Noonan_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|not_specified|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder|not_specified": 1,
    "LZTR1-related_disorder|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|Noonan_syndrome": 1,
    "LZTR1-related_schwannomatosis|Noonan_syndrome|Noonan_syndrome_2": 1,
    "not_provided|Noonan_syndrome_10": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|LZTR1-related_schwannomatosis": 2,
    "not_provided|Noonan_syndrome_1|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|LZTR1-related_schwannomatosis|Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "Noonan_syndrome_2|Noonan_syndrome_10": 2,
    "Noonan_syndrome_2|LZTR1-related_disorder|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_provided|LZTR1-related_disorder|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_2|Noonan_syndrome_10|LZTR1-related_schwannomatosis|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2|not_specified|LZTR1-related_schwannomatosis": 1,
    "LZTR1-related_schwannomatosis|not_specified|not_provided|Noonan_syndrome_10|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|Schwannomatosis|Noonan_syndrome_2": 1,
    "not_provided|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_10|Noonan_syndrome_2": 1,
    "LZTR1-related_schwannomatosis|LZTR1-related_disorder|not_specified|Noonan_syndrome_2|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "LZTR1-associated_CaLMs-syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|LZTR1-related_schwannomatosis": 1,
    "not_specified|not_provided|LZTR1-related_schwannomatosis": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_disorder|Noonan_syndrome_10": 1,
    "LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_and_Noonan-related_syndrome|Noonan_syndrome_10": 1,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided|See_cases|not_specified|LZTR1-related_schwannomatosis": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|RASopathy|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Noonan_syndrome_10|LZTR1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|Noonan_syndrome_2": 1,
    "not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|Noonan_syndrome_and_Noonan-related_syndrome": 1,
    "not_provided|Noonan_syndrome_2|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis": 1,
    "Noonan_syndrome_1|not_provided|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Noonan_syndrome_10|Noonan_syndrome_2|LZTR1-related_schwannomatosis|LZTR1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|Noonan_syndrome_10|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided|LZTR1-related_disorder": 1,
    "Noonan_syndrome_2|Noonan_syndrome_1|LZTR1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_disorder": 1,
    "Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome|LZTR1-related_schwannomatosis|not_specified|not_provided": 1,
    "LZTR1-related_disorder|not_specified|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|LZTR1-related_schwannomatosis|not_provided": 1,
    "not_provided|not_specified|LZTR1-related_schwannomatosis|Cardiovascular_phenotype|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Noonan_syndrome_and_Noonan-related_syndrome|Hereditary_cancer-predisposing_syndrome|Cardiovascular_phenotype|not_provided": 1,
    "Heart|_malformation_of|Abnormal_facial_shape|Short_stature|Atypical_behavior|Specific_learning_disability|Intellectual_disability": 1,
    "Noonan_syndrome_13": 6,
    "not_provided|Abnormal_facial_shape|Microcephaly|Intellectual_disability|Specific_learning_disability|Short_stature|Atypical_behavior": 1,
    "MAPK1-related_disorder": 9,
    "not_provided|Noonan_syndrome_13|Heart|_malformation_of|Abnormal_facial_shape|Atypical_behavior|Specific_learning_disability|Intellectual_disability": 2,
    "not_provided|MAPK1-related_disorder": 2,
    "Noonan_syndrome_13|not_provided": 1,
    "not_provided|Noonan_syndrome_13|Heart|_malformation_of|Macrocephaly|Abnormal_facial_shape|Atypical_behavior|Specific_learning_disability": 1,
    "Abnormal_facial_shape|Microcephaly|Intellectual_disability|Specific_learning_disability|Short_stature|Atypical_behavior": 1,
    "Abnormal_facial_shape|Microcephaly|Intellectual_disability|Specific_learning_disability|Short_stature|Atypical_behavior|Noonan_syndrome_13": 1,
    "not_specified|MAPK1-related_disorder|not_provided": 1,
    "not_specified|TOP3B-related_neurodevelopmental_condition": 2,
    "TOP3B-related_disorder": 17,
    "TOP3B-related_disorder|not_provided": 5,
    "not_provided|TOP3B-related_disorder": 3,
    "Exstrophy-epispadias_complex|not_provided": 1,
    "Acute_lymphoid_leukemia|Chronic_myelogenous_leukemia|_BCR-ABL1_positive|not_provided": 1,
    "Chronic_myelogenous_leukemia|_BCR-ABL1_positive|Acute_lymphoid_leukemia": 3,
    "Agammaglobulinemia_2|_autosomal_recessive": 157,
    "not_provided|Agammaglobulinemia_2|_autosomal_recessive": 18,
    "Agammaglobulinemia_2|_autosomal_recessive|not_specified": 9,
    "not_specified|Agammaglobulinemia_2|_autosomal_recessive": 15,
    "Agammaglobulinemia_2|_autosomal_recessive|not_provided": 11,
    "not_specified|not_provided|Agammaglobulinemia_2|_autosomal_recessive": 1,
    "not_provided|Agammaglobulinemia_2|_autosomal_recessive|not_specified": 1,
    "IGLL1-related_condition|not_specified|not_provided|Agammaglobulinemia_2|_autosomal_recessive": 1,
    "Agammaglobulinemia_2|_autosomal_recessive|IGLL1-related_condition": 1,
    "IGLL1-related_condition|Agammaglobulinemia_2|_autosomal_recessive|not_specified": 1,
    "Agammaglobulinemia_2|_autosomal_recessive|not_specified|not_provided": 2,
    "not_specified|Agammaglobulinemia_2|_autosomal_recessive|not_provided": 1,
    "CHCHD10-related_disorder": 8,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 18,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset": 8,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 59,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset": 31,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|not_specified": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 10,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|not_provided|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "not_specified|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|CHCHD10-related_disorder|not_provided": 1,
    "CHCHD10-related_disorder|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "CHCHD10-related_disorder|Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|not_provided": 2,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 14,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|CHCHD10-related_disorder|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "not_specified|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 1,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|CHCHD10-related_disorder": 3,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|not_provided": 4,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Inborn_genetic_diseases|not_provided": 1,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Inborn_genetic_diseases": 2,
    "CHCHD10-related_disorder|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 1,
    "Inborn_genetic_diseases|CHCHD10-related_disorder|not_provided|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset": 1,
    "CHCHD10-related_disorder|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 1,
    "not_provided|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset": 2,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|not_specified": 1,
    "Inborn_genetic_diseases|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 2,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|not_provided|not_specified": 1,
    "not_specified|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset": 1,
    "CHCHD10-related_disorder|Inborn_genetic_diseases|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|not_provided|Amyotrophic_lateral_sclerosis": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|not_provided|Inborn_genetic_diseases|not_specified|CHCHD10-related_disorder": 1,
    "CHCHD10-related_disorder|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Inborn_genetic_diseases": 1,
    "not_provided|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 1,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|CHCHD10-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 2,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|not_provided": 1,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|not_provided": 1,
    "Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "not_specified|not_provided|CHCHD10-related_disorder|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2": 3,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|not_provided": 2,
    "CHCHD10-related_disorder|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Inborn_genetic_diseases": 1,
    "CHCHD10-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance": 1,
    "Lower_motor_neuron_syndrome_with_late-adult_onset": 1,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Inborn_genetic_diseases": 2,
    "CHCHD10-related_disorder|not_provided": 1,
    "Lower_motor_neuron_syndrome_with_late-adult_onset|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|not_specified": 1,
    "not_specified|Lower_motor_neuron_syndrome_with_late-adult_onset|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|not_provided": 1,
    "Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset|CHCHD10-related_disorder": 1,
    "not_provided|CHCHD10-related_disorder|Frontotemporal_dementia_and/or_amyotrophic_lateral_sclerosis_2|Autosomal_dominant_mitochondrial_myopathy_with_exercise_intolerance|Lower_motor_neuron_syndrome_with_late-adult_onset": 1,
    "SMARCB1-related_schwannomatosis|Rhabdoid_tumor_predisposition_syndrome_1|not_provided": 3,
    "SMARCB1-related_schwannomatosis|Rhabdoid_tumor_predisposition_syndrome_1": 12,
    "Rhabdoid_tumor_predisposition_syndrome|Coffin-Siris_syndrome|Schwannomatosis": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis": 4,
    "Rhabdoid_tumor_predisposition_syndrome_1|not_provided|SMARCB1-related_schwannomatosis": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|not_provided": 2,
    "Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|Intellectual_disability|_autosomal_dominant_15|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "SMARCB1-related_schwannomatosis": 11,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|Intellectual_disability|_autosomal_dominant_15": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1": 12,
    "not_provided|Hereditary_cancer-predisposing_syndrome|SMARCB1-related_schwannomatosis": 2,
    "not_provided|SMARCB1-related_disorder|Hereditary_cancer-predisposing_syndrome": 4,
    "Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_15": 1,
    "not_provided|SMARCB1-related_disorder": 4,
    "Intellectual_disability|_autosomal_dominant_15": 10,
    "SMARCB1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 3,
    "SMARCB1-related_disorder|not_provided": 2,
    "SMARCB1-related_BAFopathy|Coffin-Siris_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_15": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_1": 2,
    "SMARCB1-related_schwannomatosis|not_provided": 1,
    "SMARCB1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome|SMARCB1-related_schwannomatosis": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome": 5,
    "Hereditary_cancer-predisposing_syndrome|Developmental_disorder|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1|not_provided|Hereditary_cancer-predisposing_syndrome": 3,
    "Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_1": 3,
    "Teratoid_tumor|_atypical": 1,
    "Coffin-Siris_syndrome|not_provided|SMARCB1-related_schwannomatosis|Rhabdoid_tumor_predisposition_syndrome_1|not_specified": 1,
    "Schwannomatosis|not_provided": 1,
    "SMARCB1-related_schwannomatosis|Intellectual_disability|_autosomal_dominant_15|Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "SMARCB1-related_disorder|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_15|SMARCB1-related_disorder": 1,
    "not_provided|Malignant_neoplasm_of_nervous_system": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1|not_provided": 5,
    "not_provided|not_specified|SMARCB1-related_disorder|Coffin-Siris_syndrome": 1,
    "SMARCB1-related_disorder": 6,
    "Intellectual_disability|_autosomal_dominant_15|SMARCB1-related_schwannomatosis|Rhabdoid_tumor_predisposition_syndrome_1": 2,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_1": 2,
    "Schwannomatosis_1|_somatic": 1,
    "not_provided|Autism_spectrum_disorder|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|SMARCB1-related_disorder|not_provided": 2,
    "Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_2|SMARCB1-related_schwannomatosis|Intellectual_disability|_autosomal_dominant_15|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_15|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCB1-related_schwannomatosis|Rhabdoid_tumor_predisposition_syndrome_1|Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Intellectual_disability|_autosomal_dominant_15": 1,
    "not_provided|Ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|Intellectual_disability|_autosomal_dominant_15|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis": 1,
    "not_provided|Intellectual_disability|_autosomal_dominant_15": 2,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome|Schwannomatosis|Coffin-Siris_syndrome|not_provided": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|SMARCB1-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|Rhabdoid_tumor_predisposition_syndrome_1|not_provided": 2,
    "not_provided|SMARCB1-related_schwannomatosis|Rhabdoid_tumor_predisposition_syndrome_1|Intellectual_disability|_autosomal_dominant_15|Hereditary_cancer-predisposing_syndrome": 1,
    "Intellectual_disability|_autosomal_dominant_15|SMARCB1-related_BAFopathy": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|not_specified": 2,
    "Malignant_rhabdoid_tumor|_somatic": 1,
    "SMARCB1-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided|SMARCB1-related_schwannomatosis": 1,
    "SMARCB1-related_disorder|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCB1-related_disorder|Rhabdoid_tumor_predisposition_syndrome_1": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Intellectual_disability|_autosomal_dominant_15": 1,
    "Intellectual_disability|_autosomal_dominant_15|Hereditary_cancer-predisposing_syndrome": 1,
    "SMARCB1-related_schwannomatosis|Intellectual_disability|_autosomal_dominant_15|Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_15|not_provided|SMARCB1-related_BAFopathy": 1,
    "Intellectual_disability|_autosomal_dominant_15|not_provided": 3,
    "not_provided|Intellectual_disability|_autosomal_dominant_15|Rhabdoid_tumor_predisposition_syndrome_1|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Intellectual_disability|_autosomal_dominant_15": 1,
    "Coffin-Siris_syndrome|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Coffin-Siris_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|SMARCB1-related_BAFopathy|Intellectual_disability|_autosomal_dominant_15": 1,
    "Intellectual_disability|_autosomal_dominant_15|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|SMARCB1-related_disorder|not_specified|not_provided|Rhabdoid_tumor_predisposition_syndrome_1": 1,
    "not_provided|SMARCB1-related_disorder|Rhabdoid_tumor_predisposition_syndrome_1|Hereditary_cancer-predisposing_syndrome": 1,
    "Coffin-Siris_syndrome|Rhabdoid_tumor_predisposition_syndrome|Schwannomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Coffin-Siris_syndrome|Peripheral_schwannoma|Schwannoma|SMARCB1-related_schwannomatosis": 1,
    "not_provided|Rhabdoid_tumor_predisposition_syndrome|Schwannomatosis": 1,
    "MIF-related_disorder": 3,
    "not_provided|CABIN1-related_disorder": 16,
    "CABIN1-related_disorder": 24,
    "CABIN1-related_disorder|not_specified|not_provided": 1,
    "CABIN1-related_disorder|not_provided": 9,
    "CABIN1-related_disorder|not_specified": 1,
    "not_provided|SPECC1L-related_disorder": 5,
    "SPECC1L-related_disorder|not_provided": 9,
    "SPECC1L-related_disorder": 18,
    "Oculomaxillofacial_dysostosis|Teebi_hypertelorism_syndrome_1|not_provided|SPECC1L-related_disorder": 1,
    "Teebi_hypertelorism_syndrome_1": 9,
    "not_specified|SPECC1L-related_disorder|Teebi_hypertelorism_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "SPECC1L-related_syndrome": 1,
    "SPECC1L-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Oculomaxillofacial_dysostosis|Teebi_hypertelorism_syndrome_1": 1,
    "Oculomaxillofacial_dysostosis|Teebi_hypertelorism_syndrome_1": 3,
    "Teebi_hypertelorism_syndrome_1|Inborn_genetic_diseases": 1,
    "Oculomaxillofacial_dysostosis|Teebi_hypertelorism_syndrome_1|not_provided": 1,
    "Autosomal_dominant_Opitz_G/BBB_syndrome|Teebi_hypertelorism_syndrome|not_specified|Oculomaxillofacial_dysostosis|not_provided": 1,
    "not_provided|not_specified|SPECC1L-related_disorder": 1,
    "Teebi_hypertelorism_syndrome": 5,
    "Teebi_hypertelorism_syndrome_1|not_provided|Teebi_hypertelorism_syndrome": 1,
    "Oculomaxillofacial_dysostosis": 2,
    "not_provided|Teebi_hypertelorism_syndrome_1|Teebi_hypertelorism_syndrome": 1,
    "Teebi_hypertelorism_syndrome_1|Teebi_hypertelorism_syndrome": 2,
    "Autosomal_dominant_Opitz_G/BBB_syndrome": 3,
    "Teebi_hypertelorism_syndrome|Inborn_genetic_diseases": 1,
    "SPECC1L-related_disorder|not_specified|not_provided": 2,
    "not_provided|Teebi_hypertelorism_syndrome_1|Oculomaxillofacial_dysostosis|not_specified": 1,
    "not_specified|Teebi_hypertelorism_syndrome": 1,
    "Oculomaxillofacial_dysostosis|Teebi_hypertelorism_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "SPECC1L-related_disorder|Teebi_hypertelorism_syndrome|not_specified|not_provided": 1,
    "not_specified|not_provided|SPECC1L-related_disorder": 2,
    "Inborn_genetic_diseases|Autosomal_dominant_Opitz_G/BBB_syndrome": 1,
    "SPECC1L-related_disorder|Teebi_hypertelorism_syndrome_1|Oculomaxillofacial_dysostosis|not_provided": 1,
    "Teebi_hypertelorism_syndrome_1|Oculomaxillofacial_dysostosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SPECC1L-related_disorder|not_provided": 1,
    "not_provided|Autosomal_dominant_Opitz_G/BBB_syndrome": 1,
    "Autosomal_dominant_Opitz_G/BBB_syndrome|Teebi_hypertelorism_syndrome|not_provided|Oculomaxillofacial_dysostosis": 1,
    "Teebi_hypertelorism_syndrome_1|Oculomaxillofacial_dysostosis|not_provided": 1,
    "not_provided|Teebi_hypertelorism_syndrome|Autosomal_dominant_Opitz_G/BBB_syndrome|Oculomaxillofacial_dysostosis": 1,
    "Autosomal_dominant_Opitz_G/BBB_syndrome|Teebi_hypertelorism_syndrome": 1,
    "Teebi_hypertelorism_syndrome_1|not_provided": 1,
    "Inborn_genetic_diseases|SPECC1L-related_disorder": 1,
    "Teebi_hypertelorism_syndrome_1|Teebi_hypertelorism_syndrome|not_provided|SPECC1L-related_syndrome": 1,
    "not_provided|Deficiency_of_beta-ureidopropionase": 18,
    "Deficiency_of_beta-ureidopropionase": 35,
    "Deficiency_of_beta-ureidopropionase|not_provided": 10,
    "Inborn_genetic_diseases|not_provided|Deficiency_of_beta-ureidopropionase": 1,
    "Deficiency_of_beta-ureidopropionase|UPB1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Deficiency_of_beta-ureidopropionase": 4,
    "not_specified|not_provided|Deficiency_of_beta-ureidopropionase": 1,
    "not_provided|Deficiency_of_beta-ureidopropionase|Inborn_genetic_diseases": 1,
    "UPB1-related_disorder|not_provided|Deficiency_of_beta-ureidopropionase": 3,
    "Deficiency_of_beta-ureidopropionase|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Deficiency_of_beta-ureidopropionase": 2,
    "UPB1-related_disorder": 3,
    "Deficiency_of_beta-ureidopropionase|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deficiency_of_beta-ureidopropionase|UPB1-related_disorder|not_provided": 1,
    "UPB1-related_disorder|Deficiency_of_beta-ureidopropionase|not_provided": 1,
    "Deficiency_of_beta-ureidopropionase|UPB1-related_disorder|not_provided": 1,
    "gamma-Glutamyltransferase_deficiency": 1,
    "not_provided|gamma-Glutamyltransferase_deficiency": 1,
    "Cataract_22_multiple_types": 35,
    "Congenital_nuclear_cataract|Cataract_22_multiple_types|not_provided": 1,
    "Cataract_22_multiple_types|not_provided": 2,
    "Cataract_22_multiple_types|Inborn_genetic_diseases": 2,
    "not_provided|Cataract_22_multiple_types|Inborn_genetic_diseases|Congenital_nuclear_cataract": 1,
    "Inborn_genetic_diseases|Cataract_22_multiple_types": 9,
    "not_provided|Cataract_22_multiple_types|Inborn_genetic_diseases": 1,
    "not_provided|Cataract_22_multiple_types": 3,
    "Inborn_genetic_diseases|Cataract_22_multiple_types|not_provided": 1,
    "CRYBB3-related_disorder": 2,
    "Congenital_nuclear_cataract|not_specified|not_provided|Cataract_22_multiple_types": 1,
    "not_specified|Congenital_nuclear_cataract|Cataract_22_multiple_types|not_provided": 1,
    "Cataract|Microphthalmia": 1,
    "not_provided|Congenital_nuclear_cataract|not_specified|Cataract_22_multiple_types": 1,
    "Cataract_22_multiple_types|CRYBB3-related_disorder": 1,
    "Developmental_cataract|Cataract_22_multiple_types": 1,
    "not_provided|Cataract_22_multiple_types|CRYBB3-related_disorder": 1,
    "Cataract_22_multiple_types|not_provided|Congenital_nuclear_cataract": 1,
    "not_provided|Congenital_nuclear_cataract": 1,
    "Cataract_3_multiple_types": 48,
    "not_provided|Cataract_3_multiple_types": 3,
    "CRYBB2-related_disorder": 6,
    "CRYBB2-related_disorder|Cataract_3_multiple_types|Inborn_genetic_diseases": 1,
    "not_provided|Cataract_3_multiple_types|not_specified": 2,
    "Developmental_cataract|not_provided|CRYBB2-related_disorder|Cataract_3_multiple_types": 1,
    "not_provided|not_specified|Cataract_3_multiple_types": 1,
    "Cataract_3_multiple_types|not_provided|CRYBB2-related_disorder|not_specified": 1,
    "not_provided|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 41,
    "not_provided|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|Inborn_genetic_diseases": 12,
    "not_provided|MYO18B-related_disorder": 33,
    "Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|not_provided": 38,
    "Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 39,
    "MYO18B-related_disorder|not_provided|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 2,
    "Inborn_genetic_diseases|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 2,
    "MYO18B-related_disorder|not_provided": 34,
    "not_provided|Inborn_genetic_diseases|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 4,
    "MYO18B-related_disorder": 11,
    "MYO18B-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|MYO18B-related_disorder|Inborn_genetic_diseases": 5,
    "MYO18B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|MYO18B-related_disorder": 1,
    "Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|Inborn_genetic_diseases|not_provided": 6,
    "Inborn_genetic_diseases|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|MYO18B-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 1,
    "not_provided|MYO18B-related_disorder|not_specified|Limb-girdle_muscular_dystrophy": 1,
    "MYO18B-related_disorder|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|not_provided": 1,
    "not_provided|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|MYO18B-related_disorder": 1,
    "Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|Klippel-Feil_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|MYO18B-related_disorder|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 1,
    "not_provided|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|Inborn_genetic_diseases|MYO18B-related_disorder": 1,
    "Nemaline_myopathy|Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome": 1,
    "not_specified|MYO18B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Klippel-Feil_anomaly-myopathy-facial_dysmorphism_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|MYO18B-related_disorder": 1,
    "not_provided|MYO18B-related_disorder|not_specified": 1,
    "Hermansky-Pudlak_syndrome_4": 102,
    "not_provided|Hermansky-Pudlak_syndrome_4": 18,
    "Hermansky-Pudlak_syndrome_4|not_provided": 22,
    "HPS4-related_disorder": 5,
    "not_provided|HPS4-related_disorder": 7,
    "Hermansky-Pudlak_syndrome_4|HPS4-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_4|not_provided": 2,
    "Hermansky-Pudlak_syndrome_4|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Hermansky-Pudlak_syndrome_4": 1,
    "Hermansky-Pudlak_syndrome_4|not_provided|not_specified|Hermansky-Pudlak_syndrome": 1,
    "HPS4-related_disorder|not_provided|Hermansky-Pudlak_syndrome_4": 3,
    "Hermansky-Pudlak_syndrome_4|not_specified|Hermansky-Pudlak_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|not_specified|Hermansky-Pudlak_syndrome_4|not_provided": 2,
    "HPS4-related_disorder|not_specified|Hermansky-Pudlak_syndrome_4|not_provided": 1,
    "not_provided|HPS4-related_disorder|Hermansky-Pudlak_syndrome_4|Inborn_genetic_diseases": 1,
    "not_provided|Hermansky-Pudlak_syndrome_4|not_specified|Hermansky-Pudlak_syndrome": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Hermansky-Pudlak_syndrome|HPS4-related_disorder": 1,
    "Hermansky-Pudlak_syndrome_4|Hermansky-Pudlak_syndrome": 1,
    "HPS4-related_disorder|Hermansky-Pudlak_syndrome_4|not_provided": 3,
    "not_provided|Hermansky-Pudlak_syndrome_4|Hermansky-Pudlak_syndrome": 1,
    "not_provided|not_specified|Hermansky-Pudlak_syndrome_4": 1,
    "Hermansky-Pudlak_syndrome_4|not_provided|not_specified": 2,
    "Hermansky-Pudlak_syndrome_4|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_4": 3,
    "Inborn_genetic_diseases|not_provided|Hermansky-Pudlak_syndrome_4|not_specified": 1,
    "Inborn_genetic_diseases|HPS4-related_disorder": 1,
    "not_provided|Hermansky-Pudlak_syndrome_4|Oculocutaneous_albinism|not_specified|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_4|HPS4-related_disorder|not_provided": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome_4|Hermansky-Pudlak_syndrome": 1,
    "Hermansky-Pudlak_syndrome_4|HPS4-related_disorder": 1,
    "not_specified|Hermansky-Pudlak_syndrome_4|not_provided": 1,
    "HPS4-related_disorder|Hermansky-Pudlak_syndrome_4|not_provided|not_specified": 1,
    "Hermansky-Pudlak_syndrome_4|not_provided|Hermansky-Pudlak_syndrome|not_specified": 1,
    "not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_4|See_cases": 1,
    "HPS4-related_disorder|not_provided": 3,
    "HPS4-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "HPS4-related_disorder|Hermansky-Pudlak_syndrome_4|not_specified": 1,
    "Hermansky-Pudlak_syndrome_4|not_specified": 1,
    "HPS4-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Hermansky-Pudlak_syndrome_4|Inborn_genetic_diseases": 1,
    "Hermansky-Pudlak_syndrome_4|See_cases|not_provided": 1,
    "not_provided|not_specified|HPS4-related_disorder": 1,
    "not_specified|not_provided|Hermansky-Pudlak_syndrome|Hermansky-Pudlak_syndrome_4": 1,
    "Inborn_genetic_diseases|Hermansky-Pudlak_syndrome_4": 2,
    "Cataract_17_multiple_types": 39,
    "CRYBB1-related_disorder": 3,
    "CRYBB1-related_disorder|Cataract_17_multiple_types": 2,
    "Cataract_17_multiple_types|CRYBB1-related_disorder": 4,
    "not_provided|Cataract_17_multiple_types": 4,
    "Inborn_genetic_diseases|Cataract_17_multiple_types": 4,
    "Cataract_17_multiple_types|not_provided": 2,
    "Cataract_17_multiple_types|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Cataract_17_multiple_types": 1,
    "Cataract_17|Cataract_17_multiple_types|not_provided": 1,
    "Cataract_23": 41,
    "not_provided|Cataract_23|Developmental_cataract": 1,
    "Inborn_genetic_diseases|Cataract_23": 1,
    "Cataract_23|Inborn_genetic_diseases": 3,
    "not_provided|Cataract_23|not_specified": 4,
    "Cataract_23|CRYBA4-related_disorder": 1,
    "Cataract_23|not_specified|not_provided": 1,
    "not_provided|Cataract_23": 1,
    "not_provided|Cataract_23|CRYBA4-related_disorder": 2,
    "Cataract_23|CRYBA4-related_disorder|not_provided": 1,
    "Cataract_23|not_provided": 1,
    "CRYBA4-related_disorder|Cataract_23|not_provided": 1,
    "CRYBA4-related_disorder": 1,
    "MIAT-related_disorder": 13,
    "MN1_C-terminal_truncation_(MCTT)_syndrome|not_provided|Familial_meningioma|CEBALID_syndrome": 1,
    "MN1_C-terminal_truncation_(MCTT)_syndrome": 3,
    "CEBALID_syndrome|MN1_C-terminal_truncation_(MCTT)_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "CEBALID_syndrome|MN1_C-terminal_truncation_(MCTT)_syndrome": 3,
    "MN1-related_disorder": 19,
    "Atrial_septal_defect|Congenital_diaphragmatic_hernia|MN1_C-terminal_truncation_(MCTT)_syndrome": 1,
    "CEBALID_syndrome|MN1_C-terminal_truncation_(MCTT)_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|MN1-related_disorder": 1,
    "not_provided|MN1-related_disorder": 6,
    "Inborn_genetic_diseases|MN1-related_disorder": 5,
    "MN1-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Familial_meningioma|CEBALID_syndrome": 2,
    "MN1-related_disorder|not_provided": 3,
    "Familial_meningioma|CEBALID_syndrome|not_provided": 1,
    "CEBALID_syndrome|not_provided": 1,
    "Hepatoblastoma|MN1-related_disorder": 1,
    "Familial_meningioma|CEBALID_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|MN1-related_disorder": 1,
    "CEBALID_syndrome|MN1-related_disorder": 1,
    "not_provided|CEBALID_syndrome": 1,
    "not_specified|not_provided|TTC28-related_disorder": 2,
    "TTC28-related_disorder": 22,
    "TTC28-related_disorder|not_provided": 2,
    "TTC28-related_disorder|not_specified": 1,
    "not_provided|TTC28-related_disorder": 3,
    "CHEK2-related_cancer_predisposition": 17,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Malignant_tumor_of_breast|not_provided": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_nonpolyposis_colon_cancer": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|CHEK2-related_cancer_predisposition": 2,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_cancer_predisposition|not_provided": 1,
    "not_provided|Malignant_tumor_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Predisposition_to_cancer": 1,
    "not_specified|CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 3,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|Li-Fraumeni_syndrome": 1,
    "CHEK2-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_prostate_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_disorder|Breast_and/or_ovarian_cancer": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer|CHEK2-related_disorder|Predisposition_to_cancer|Familial_cancer_of_breast|Prostate_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Gastric_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and_colorectal_cancer|_susceptibility_to": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer": 3,
    "CHEK2-related_disorder|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|Bone_osteosarcoma|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Familial_colorectal_cancer_type_X|Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|CHEK2-related_disorder|Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|not_specified": 1,
    "not_specified|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Prostate_cancer|Bone_osteosarcoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|not_provided|Familial_cancer_of_breast": 1,
    "not_provided|Incidental_Discovery|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_provided|Li-Fraumeni_syndrome_1|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 7,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 2,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|CHEK2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Hereditary_nonpolyposis_colon_cancer|not_specified|not_provided": 2,
    "Familial_cancer_of_breast|not_provided|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 4,
    "Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Colorectal_cancer|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|CHEK2-related_disorder|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and_colorectal_cancer|_susceptibility_to|Colon_cancer|Breast_carcinoma|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 3,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition": 3,
    "Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|NK-cell_enteropathy": 1,
    "CHEK2-related_disorder|Predisposition_to_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "Prostate_cancer|Familial_cancer_of_breast|Lung_carcinoma|Carcinoma_of_colon|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|Familial_cancer_of_breast": 3,
    "CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_disorder|not_provided": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma": 2,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 4,
    "not_provided|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Predisposition_to_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Bone_osteosarcoma|Prostate_cancer|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Prostate_cancer|Bone_osteosarcoma|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Predisposition_to_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Predisposition_to_cancer|Familial_cancer_of_breast|Prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_disorder|not_provided": 1,
    "Hereditary_cancer|CHEK2-related_disorder|Breast_and/or_ovarian_cancer|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_colon|Malignant_tumor_of_breast": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Inherited_breast_cancer_and_ovarian_cancer|CHEK2-related_disorder|TUMOR_PREDISPOSITION_SYNDROME_4|_BREAST|CHEK2-related_cancer_risk|Familial_cancer_of_breast|Prostate_cancer|Breast_and/or_ovarian_cancer|Breast_neoplasm|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and_colorectal_cancer|_susceptibility_to|Breast_cancer|_susceptibility_to|Malignant_tumor_of_breast": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_prostate_cancer": 1,
    "CHEK2-related_disorder|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Prostate_cancer|Familial_cancer_of_breast|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|CHEK2-related_disorder|Familial_cancer_of_breast|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CHEK2-related_disorder|Predisposition_to_cancer|Cancer_or_benign_tumor|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Familial_cancer_of_breast": 1,
    "not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Familial_cancer_of_breast": 2,
    "Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Bone_osteosarcoma|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Predisposition_to_cancer|CHEK2-related_disorder|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Malignant_tumor_of_breast": 1,
    "not_provided|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 4,
    "Familial_cancer_of_breast|CHEK2-related_disorder": 2,
    "CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 3,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 4,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_disorder": 3,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|not_provided|Malignant_tumor_of_breast|not_specified|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_specified|not_provided|Hereditary_nonpolyposis_colon_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Premature_ovarian_failure|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Breast_and/or_ovarian_cancer|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_disorder|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_disorder|CHEK2-related_cancer_predisposition|Prostate_cancer|Bone_osteosarcoma|not_specified|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|CHEK2-related_disorder|CHEK2-related_cancer_predisposition|Prostate_cancer|Bone_osteosarcoma|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CHEK2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Inherited_breast_cancer_and_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Lung_cancer|Ovarian_neoplasm|CHEK2-related_disorder|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_neoplasm|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Inherited_prostate_cancer|NICE_approved_PARP_inhibitor_treatment|Inherited_breast_cancer_and_ovarian_cancer|Predisposition_to_cancer|CHEK2-related_disorder|Leiomyosarcoma|Breast_neoplasm|TUMOR_PREDISPOSITION_SYNDROME_4|_BREAST/PROSTATE/COLORECTAL|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Astrocytoma|not_provided|Ovarian_neoplasm|Hereditary_breast_ovarian_cancer_syndrome|Carcinoma_of_pancreas|Li-Fraumeni_syndrome|Li-Fraumeni_syndrome_1|Breast_and_colorectal_cancer|_susceptibility_to|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_cancer|_susceptibility_to|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|not_provided|Familial_cancer_of_breast": 1,
    "Bone_osteosarcoma|Colorectal_cancer|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Predisposition_to_cancer": 1,
    "Carcinoma_of_pancreas|Familial_cancer_of_breast|TUMOR_PREDISPOSITION_SYNDROME_4|_BREAST/PROSTATE|not_provided": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Familial_cancer_of_breast|Malignant_lymphoma|_large_B-cell|_diffuse": 1,
    "Li-Fraumeni_syndrome|Familial_cancer_of_breast": 1,
    "Malignant_tumor_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|not_specified|not_provided|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Triple-negative_breast_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Bone_osteosarcoma|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|not_provided": 1,
    "not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Prostate_cancer|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Malignant_tumor_of_breast": 2,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition": 2,
    "Hereditary_cancer-predisposing_syndrome|Predisposition_to_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_cancer_of_breast|Prostate_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|not_provided|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder": 8,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Prostate_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 4,
    "Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_disorder": 1,
    "Malignant_tumor_of_breast|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_disorder|Familial_cancer_of_breast": 4,
    "Familial_cancer_of_breast|not_specified|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_disorder|Breast_and/or_ovarian_cancer|Prostate_cancer": 1,
    "not_provided|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|Bone_osteosarcoma": 2,
    "Colorectal_cancer|Prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CHEK2-related_disorder|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|Colorectal_cancer|CHEK2-related_cancer_predisposition|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|not_provided": 1,
    "Prostate_cancer|Bone_osteosarcoma|Familial_cancer_of_breast|Colorectal_cancer|CHEK2-related_cancer_predisposition|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Bone_osteosarcoma|Prostate_cancer|Colorectal_cancer|CHEK2-related_cancer_predisposition|not_provided": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Carcinoma_of_pancreas|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Colonic_neoplasm|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_disorder|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_disorder|not_specified": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|Bone_osteosarcoma": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|CHEK2-related_disorder": 1,
    "Familial_colorectal_cancer_type_X|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_specified|Carcinoma_of_colon|CHEK2-related_disorder|not_provided": 1,
    "CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Uterine_corpus_cancer|Hereditary_cancer-predisposing_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|not_specified|Familial_cancer_of_breast": 1,
    "Prostate_cancer|Colorectal_cancer|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_provided|CHEK2-related_cancer_predisposition": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_nonpolyposis_colon_cancer|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma|Bone_osteosarcoma|Familial_prostate_cancer|Carcinoma_of_pancreas|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|CHEK2-related_disorder|Hereditary_nonpolyposis_colon_cancer": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 2,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_disorder": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Colorectal_cancer|Prostate_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Ovarian_carcinoma": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome": 2,
    "Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|Prostate_cancer|Bone_osteosarcoma|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Colorectal_cancer|Bone_osteosarcoma|Prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Li-Fraumeni_syndrome": 1,
    "not_specified|not_provided|CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_ovarian_cancer|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_disorder|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Prostate_cancer|Familial_cancer_of_breast": 1,
    "Predisposition_to_cancer|CHEK2-related_disorder|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_disorder|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Bone_osteosarcoma|Familial_prostate_cancer|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|not_provided|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|Colorectal_cancer|Bone_osteosarcoma": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|CHEK2-related_disorder|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Gastric_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Prostate_cancer": 1,
    "not_provided|Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Predisposition_to_cancer|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|not_specified": 1,
    "Breast_cancer|_susceptibility_to|Prostate_cancer_susceptibility|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|not_specified": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Prostate_cancer|Bone_osteosarcoma|Colorectal_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|Breast-ovarian_cancer|_familial|_susceptibility_to|_1": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Li-Fraumeni_syndrome": 1,
    "CHEK2-related_disorder|not_specified|Familial_cancer_of_breast|not_provided": 1,
    "not_specified|not_provided|Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_disorder|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Breast_carcinoma|Malignant_tumor_of_breast": 1,
    "Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_prostate_cancer": 1,
    "Childhood_neoplasm|Inherited_breast_cancer_and_ovarian_cancer|CHEK2-related_disorder|Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Malignant_tumor_of_breast": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Colorectal_cancer|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|not_provided|not_specified": 1,
    "Malignant_tumor_of_breast|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|not_specified|not_provided": 1,
    "Predisposition_to_cancer|CHEK2-related_disorder|Prostate_cancer|Bone_osteosarcoma|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Endometrial_carcinoma": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Breast_and_colorectal_cancer|_susceptibility_to|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Breast_and/or_ovarian_cancer|Prostate_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2|Malignant_tumor_of_breast": 1,
    "CHEK2-related_disorder|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|_somatic|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Prostate_cancer|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Diffuse_midline_glioma|_H3_K27-altered|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|Familial_ovarian_cancer": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Colorectal_cancer|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|not_provided|CHEK2-related_cancer_predisposition": 1,
    "CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Hereditary_nonpolyposis_colon_cancer|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast_and_colorectal_cancer|_susceptibility_to|Familial_cancer_of_breast|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|CHEK2-related_cancer_predisposition|Breast_and_colorectal_cancer|_susceptibility_to|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Predisposition_to_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|See_cases": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "Familial_prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|CHEK2-related_disorder|Gastrointestinal_carcinoma|Adrenal_cortex_carcinoma|TUMOR_PREDISPOSITION_SYNDROME_4|_BREAST/PROSTATE/COLORECTAL|Colorectal_cancer|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided|Prostate_cancer|Breast_and_colorectal_cancer|_susceptibility_to|Cystic_fibrosis|Malignant_tumor_of_breast": 1,
    "Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|Breast_cancer|_susceptibility_to|Prostate_cancer_susceptibility": 1,
    "not_provided|not_specified|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Bone_osteosarcoma|Prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome": 1,
    "CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_cancer_of_breast": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Colorectal_cancer|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|CHEK2-related_disorder|TUMOR_PREDISPOSITION_SYNDROME_4|_BREAST/PROSTATE|Melanoma|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer|Prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Endometrial_carcinoma|Breast_and_colorectal_cancer|_susceptibility_to|Breast_cancer|_susceptibility_to|Malignant_tumor_of_breast|Breast_carcinoma": 1,
    "CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|Colorectal_cancer|Prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Gastric_cancer|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome_1|Li-Fraumeni_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Familial_colorectal_cancer_type_X|Li-Fraumeni_syndrome|CHEK2-related_disorder|Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Breast_and/or_ovarian_cancer|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Hereditary_nonpolyposis_colon_cancer|not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|not_specified|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_specified|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Bone_osteosarcoma|Prostate_cancer|not_provided|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Congenital_heart_defects|_multiple_types|_3|Gastric_cancer|CHEK2-related_cancer_predisposition|Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|Colorectal_cancer|Bone_osteosarcoma|not_provided|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_prostate_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Hereditary_cancer-predisposing_syndrome|Endometrial_carcinoma|Familial_cancer_of_breast|not_provided": 1,
    "Inherited_breast_cancer_and_ovarian_cancer|Predisposition_to_cancer|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|CHEK2-related_disorder|Breast_cancer|_susceptibility_to|Prostate_cancer_susceptibility|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Breast_carcinoma|Familial_cancer_of_breast": 1,
    "Sarcoma|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Colorectal_cancer|not_provided|Breast_neoplasm|Familial_cancer_of_breast": 1,
    "not_provided|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Malignant_tumor_of_breast|Familial_cancer_of_breast|not_provided|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "CHEK2-related_disorder|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_specified|not_provided": 1,
    "CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast": 1,
    "Breast-ovarian_cancer|_familial|_susceptibility_to|_2|CHEK2-related_disorder|Familial_cancer_of_breast|not_provided": 1,
    "Hereditary_breast_ovarian_cancer_syndrome|Bone_osteosarcoma|Colorectal_cancer|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Prostate_cancer|CHEK2-related_disorder": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_disorder": 1,
    "not_provided|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer": 1,
    "Breast_cancer|_susceptibility_to|Prostate_cancer_susceptibility|Prostate_cancer|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_provided|Malignant_tumor_of_breast": 1,
    "CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Breast_cancer|_susceptibility_to|Prostate_cancer_susceptibility|Familial_cancer_of_breast": 1,
    "Hereditary_nonpolyposis_colon_cancer|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|not_specified|not_provided|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_prostate_cancer|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Colorectal_cancer|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Prostate_cancer|Familial_cancer_of_breast|Colorectal_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|CHEK2-related_disorder|Gastric_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Li-Fraumeni_syndrome|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Breast_and_colorectal_cancer|_susceptibility_to|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Predisposition_to_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|Hereditary_breast_ovarian_cancer_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_1|Familial_cancer_of_breast|CHEK2-related_cancer_predisposition": 1,
    "not_provided|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Familial_prostate_cancer|CHEK2-related_disorder": 1,
    "CHEK2-related_disorder|Predisposition_to_cancer|Bone_osteosarcoma|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer|Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Breast_and/or_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Bone_osteosarcoma|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|not_provided|Malignant_tumor_of_breast|CHEK2-related_cancer_predisposition": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Hereditary_breast_ovarian_cancer_syndrome|Familial_cancer_of_breast|Breast_and/or_ovarian_cancer": 1,
    "Hereditary_nonpolyposis_colon_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|not_provided|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition": 1,
    "Familial_cancer_of_breast|Malignant_tumor_of_breast|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition": 1,
    "not_specified|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "Predisposition_to_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Prostate_cancer|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "CHEK2-related_disorder|not_specified|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome": 1,
    "Predisposition_to_cancer|Breast_and/or_ovarian_cancer|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|Hereditary_breast_ovarian_cancer_syndrome|Breast_and_colorectal_cancer|_susceptibility_to|Familial_cancer_of_breast|Malignant_tumor_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast|Li-Fraumeni_syndrome": 1,
    "not_provided|Familial_cancer_of_breast|Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma|Prostate_cancer": 1,
    "Hereditary_cancer-predisposing_syndrome|Prostate_cancer|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|not_specified|not_provided": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Predisposition_to_cancer": 1,
    "Prostate_cancer|Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Li-Fraumeni_syndrome|Breast-ovarian_cancer|_familial|_susceptibility_to|_2": 1,
    "not_specified|Familial_cancer_of_breast|Bone_osteosarcoma|Prostate_cancer|Colorectal_cancer|CHEK2-related_cancer_predisposition|Hereditary_nonpolyposis_colon_cancer|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Familial_cancer_of_breast|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Bone_osteosarcoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Breast_and/or_ovarian_cancer|not_provided|Familial_cancer_of_breast": 1,
    "Colorectal_cancer|Hereditary_cancer-predisposing_syndrome|Familial_cancer_of_breast": 1,
    "CHEK2-related_cancer_predisposition|Familial_cancer_of_breast|not_provided|Hereditary_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|Hereditary_nonpolyposis_colon_cancer|not_specified|Familial_cancer_of_breast": 1,
    "Familial_cancer_of_breast|Familial_prostate_cancer|CHEK2-related_cancer_predisposition|Bone_osteosarcoma|Inherited_breast_cancer_and_ovarian_cancer|Familial_ovarian_cancer|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Breast_carcinoma": 1,
    "Bone_osteosarcoma": 1,
    "Familial_cancer_of_breast|Bone_osteosarcoma|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Familial_cancer_of_breast|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_cancer_of_breast|CHEK2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "not_specified|Breast_and/or_ovarian_cancer|not_provided|Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|CHEK2-related_cancer_predisposition|Malignant_tumor_of_breast|not_specified|not_provided|Familial_cancer_of_breast": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_cancer|Malignant_tumor_of_breast|Breast_and/or_ovarian_cancer|not_provided|CHEK2-related_cancer_predisposition": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Familial_cancer_of_breast|Hereditary_breast_ovarian_cancer_syndrome|Familial_ovarian_cancer|CHEK2-related_disorder|not_provided": 1,
    "not_provided|Familial_cancer_of_breast|Malignant_tumor_of_breast|CHEK2-related_cancer_predisposition|Familial_prostate_cancer|Colorectal_cancer|Bone_osteosarcoma|Hereditary_cancer-predisposing_syndrome|not_specified|CHEK2-related_disorder": 1,
    "Anemia|_sideroblastic|_5": 4,
    "not_specified|Anemia|_sideroblastic|_5": 1,
    "Major_affective_disorder_7": 1,
    "ZNRF3-related_disorder": 9,
    "ZNRF3-related_disorder|not_provided": 1,
    "ZNRF3-associated_neurodevelopmental_disorder": 1,
    "Male_pseudohermaphroditism": 1,
    "not_provided|Ectodermal_dysplasia_13|_hair/tooth_type": 1,
    "Ectodermal_dysplasia_13|_hair/tooth_type": 4,
    "Inborn_genetic_diseases|Ectodermal_dysplasia_13|_hair/tooth_type": 1,
    "Infantile_cerebellar-retinal_degeneration": 24,
    "not_provided|KREMEN1-related_disorder": 1,
    "KREMEN1-related_disorder": 1,
    "Ectodermal_dysplasia_13|_hair/tooth_type|not_provided": 1,
    "EWSR1-related_disorder": 4,
    "Ewing_sarcoma|not_provided": 1,
    "not_provided|EWSR1-related_disorder": 1,
    "AP1B1-related_disorder": 12,
    "AP1B1-related_disorder|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_keratitis-ichthyosis-deafness_syndrome": 12,
    "Autosomal_recessive_keratitis-ichthyosis-deafness_syndrome|not_provided": 2,
    "not_provided|AP1B1-related_disorder": 1,
    "NEFH-related_disorder|Inborn_genetic_diseases|not_provided": 8,
    "not_provided|NEFH-related_disorder": 31,
    "Charcot-Marie-Tooth_disease_axonal_type_2CC": 9,
    "NEFH-related_disorder": 16,
    "NEFH-related_disorder|not_provided": 22,
    "Inborn_genetic_diseases|not_specified|not_provided|NEFH-related_disorder": 1,
    "Inborn_genetic_diseases|NEFH-related_disorder|not_provided": 4,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2CC": 5,
    "not_provided|NEFH-related_disorder|Inborn_genetic_diseases": 5,
    "NEFH-related_disorder|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|NEFH-related_disorder": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2CC|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2CC|NEFH-related_disorder|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Charcot-Marie-Tooth_disease_axonal_type_2CC|not_specified|NEFH-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Charcot-Marie-Tooth_disease_axonal_type_2CC|not_provided|not_specified": 1,
    "NEFH-related_disorder|not_provided|Peripheral_neuropathy": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2CC|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Amyotrophic_lateral_sclerosis_type_1|Charcot-Marie-Tooth_disease_axonal_type_2CC": 1,
    "NEFH-related_disorder|not_provided|Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2CC|Amyotrophic_lateral_sclerosis_type_1": 1,
    "not_specified|Inborn_genetic_diseases|NEFH-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_1|not_specified|not_provided": 1,
    "NEFH-related_disorder|Inborn_genetic_diseases": 1,
    "NEFH-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|NEFH-related_disorder": 4,
    "not_provided|Peripheral_neuropathy|Amyotrophic_lateral_sclerosis_type_1|Charcot-Marie-Tooth_disease_axonal_type_2CC": 1,
    "NEFH-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2CC|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2CC|Amyotrophic_lateral_sclerosis_type_1|NEFH-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Amyotrophic_lateral_sclerosis|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2CC|Amyotrophic_lateral_sclerosis_type_1|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2CC": 1,
    "NEFH-related_disorder|Inborn_genetic_diseases|not_provided|Amyotrophic_lateral_sclerosis_type_1": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2CC|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2CC|not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_1": 1,
    "NEFH-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|NEFH-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2CC|not_specified|Amyotrophic_lateral_sclerosis_type_1|not_provided": 1,
    "NEFH-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Neurofibromatosis|_type_2": 984,
    "Neurofibromatosis|_type_2|not_provided": 22,
    "not_provided|Neurofibromatosis|_type_2": 27,
    "Neurofibromatosis|_type_2|not_specified": 3,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 230,
    "Neurofibromatosis|_type_2|SMARCB1-related_schwannomatosis|Familial_meningioma": 1,
    "Neurofibromatosis|_type_2|Familial_meningioma": 4,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2": 294,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_specified|not_provided": 2,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2": 8,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_provided": 14,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_2|Familial_meningioma": 2,
    "Neurofibromatosis|_type_2|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 9,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_2": 24,
    "NF2-related_disorder|Familial_meningioma|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Familial_meningioma|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 2,
    "Familial_meningioma|Neurofibromatosis|_type_2": 1,
    "Familial_meningioma|SMARCB1-related_schwannomatosis|Neurofibromatosis|_type_2|not_specified": 1,
    "NF2-related_disorder|Neurofibromatosis|_type_2": 3,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Meningioma|Neurofibromatosis|_type_2": 1,
    "Neurofibromatosis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 5,
    "Neurofibromatosis|_type_2|Acoustic_neuroma": 1,
    "Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Neurofibromatosis|_type_2": 6,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_2|Familial_meningioma|SMARCB1-related_schwannomatosis": 1,
    "not_provided|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 16,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|Acoustic_neuroma": 1,
    "not_specified|not_provided|NF2-related_disorder|Neurofibromatosis|_type_2": 1,
    "Neurofibromatosis|_type_2|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "NF2-related_disorder|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_provided": 1,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified": 2,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 10,
    "Familial_meningioma|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 5,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|SMARCB1-related_schwannomatosis": 1,
    "NF2-related_disorder|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_2": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2": 8,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 6,
    "not_specified|Neurofibromatosis|_type_2": 5,
    "not_specified|Neurofibromatosis|_type_2|not_provided": 1,
    "Malignant_neoplasm_of_nervous_system|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2": 2,
    "Neurofibromatosis|_type_2|SMARCB1-related_schwannomatosis": 1,
    "Hereditary_cancer-predisposing_syndrome|NF2-related_disorder|Neurofibromatosis|_type_2": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_specified": 1,
    "Neurofibromatosis|_type_2|Familial_meningioma|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|NF2-related_disorder|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_provided": 1,
    "Spindle_cell_sarcoma": 1,
    "not_provided|Neurofibromatosis|_type_2|NF2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "Bilateral_vestibular_schwannoma": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|SMARCB1-related_schwannomatosis|Familial_meningioma": 1,
    "Familial_meningioma|not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2": 1,
    "not_provided|Neurofibromatosis|_type_2|Familial_meningioma|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_specified": 3,
    "NF2-related_disorder|not_provided|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Acoustic_neuroma": 1,
    "Neurofibromatosis|_type_2|NF2-related_disorder": 1,
    "NF2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|Familial_meningioma": 3,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|NF2-related_disorder": 4,
    "Neurofibromatosis|_type_2|Meningioma|not_specified|not_provided": 1,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|NF2-related_disorder": 2,
    "Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma|Neurofibromatosis|_type_2": 1,
    "Hereditary_cancer|not_specified|Neurofibromatosis|_type_2|Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Meningioma": 3,
    "Neurofibromatosis|_type_2|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_meningioma|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided": 1,
    "Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided|Familial_meningioma": 2,
    "Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_2": 3,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Neurofibromatosis|_type_2": 1,
    "Familial_meningioma|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Neurofibromatosis|_type_2|SMARCB1-related_schwannomatosis": 1,
    "Familial_meningioma|Neurofibromatosis|_type_2|SMARCB1-related_schwannomatosis|Hereditary_cancer-predisposing_syndrome": 1,
    "Familial_meningioma|Neurofibromatosis|_type_2|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_2|NF2-related_disorder|not_provided|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Neurofibromatosis|_type_2|NF2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Neurofibromatosis|_type_2|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "NF2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_2": 1,
    "Neurofibromatosis|_type_2|NF2-related_disorder|not_specified|not_provided|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|Familial_meningioma": 1,
    "Familial_meningioma|SMARCB1-related_schwannomatosis|Neurofibromatosis|_type_2": 1,
    "not_specified|NF2-related_disorder|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|Familial_meningioma": 1,
    "Neurofibromatosis|_type_2|not_provided|NF2-related_disorder|Hereditary_cancer-predisposing_syndrome": 2,
    "not_specified|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_provided|Familial_meningioma|NF2-related_disorder": 1,
    "Neurofibromatosis|_type_2|NF2-related_disorder|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|Familial_meningioma": 1,
    "NF2-related_disorder|Hereditary_cancer-predisposing_syndrome|Familial_meningioma|Neurofibromatosis|_type_2": 1,
    "Hereditary_cancer-predisposing_syndrome|Neurofibromatosis|_type_2|not_provided|Familial_meningioma": 1,
    "NF2-related_disorder|Neurofibromatosis|_type_2|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Hereditary_cancer-predisposing_syndrome|SMARCB1-related_schwannomatosis|Familial_meningioma|Neurofibromatosis|_type_2": 1,
    "NF2-related_disorder|not_specified|not_provided|Neurofibromatosis|_type_2": 1,
    "NF2-related_disorder|Hereditary_cancer-predisposing_syndrome|not_provided|Neurofibromatosis|_type_2|Malignant_tumor_of_breast": 1,
    "Neurofibromatosis|_type_2|Familial_meningioma|SMARCB1-related_schwannomatosis|not_provided": 1,
    "not_provided|Transcobalamin_II_deficiency": 32,
    "Transcobalamin_II_deficiency": 551,
    "Transcobalamin_II_deficiency|Inborn_genetic_diseases": 21,
    "Transcobalamin_II_deficiency|not_provided": 16,
    "TCN2-related_disorder|not_provided|Transcobalamin_II_deficiency": 3,
    "Transcobalamin_II_deficiency|TCN2-related_disorder": 8,
    "Transcobalamin_II_deficiency|not_provided|TCN2-related_disorder": 1,
    "not_specified|Transcobalamin_II_deficiency": 1,
    "not_provided|Transcobalamin_II_deficiency|not_specified|TCN2-related_disorder": 1,
    "TCN2-related_disorder|Transcobalamin_II_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Transcobalamin_II_deficiency": 3,
    "Inborn_genetic_diseases|Transcobalamin_II_deficiency": 11,
    "TCN2-related_disorder|Transcobalamin_II_deficiency": 2,
    "Transcobalamin_II_deficiency|Pancytopenia|not_provided": 1,
    "TCN2-related_disorder|Transcobalamin_II_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|TCN2_POLYMORPHISM|Transcobalamin_II_deficiency": 1,
    "Transcobalamin_II_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Transcobalamin_II_deficiency": 1,
    "TCN2-related_disorder": 1,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy": 12,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z": 635,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|Inborn_genetic_diseases": 12,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy": 5,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 33,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z": 16,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Charcot-Marie-Tooth_disease_axonal_type_2Z": 6,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|not_specified": 8,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided|Tip-toe_gait": 1,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Z": 2,
    "MORC2-related_disorder": 7,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|See_cases": 1,
    "not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|MORC2-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Z|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Inborn_genetic_diseases": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Z": 14,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided|Inborn_genetic_diseases": 1,
    "MORC2-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2Z": 5,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Charcot-Marie-Tooth_disease_axonal_type_2Z": 3,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 3,
    "MORC2-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2Z": 5,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 2,
    "not_specified|Charcot-Marie-Tooth_disease_axonal_type_2Z|Inborn_genetic_diseases": 1,
    "not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Charcot-Marie-Tooth_disease_axonal_type_2Z|MORC2-related_disorder": 1,
    "Neuronopathy|_distal_hereditary_motor|_autosomal_dominant|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|MORC2-related_disorder": 5,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|not_provided": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 3,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|MORC2-related_disorder|Charcot-Marie-Tooth_disease_axonal_type_2Z|not_provided": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|MORC2-related_disorder|not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z": 2,
    "Tip-toe_gait|See_cases|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Distal_spinal_muscular_atrophy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_axonal_type_2Z": 2,
    "not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy": 1,
    "Charcot-Marie-Tooth_disease_axonal_type_2Z|MORC2-related_disorder|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|not_provided|MORC2-related_developmental_disorder|Neurodevelopmental_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|Charcot-Marie-Tooth_disease|not_provided|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Global_developmental_delay": 1,
    "not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Z|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_axonal_type_2Z|MORC2-related_disorder|not_provided|MORC2-related_neurodevelopmental_disorders|Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|Neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "Developmental_delay|_impaired_growth|_dysmorphic_facies|_and_axonal_neuropathy|not_specified|not_provided|Charcot-Marie-Tooth_disease_axonal_type_2Z": 1,
    "Tan-Almurshedi_syndrome": 4,
    "Liberfarb_syndrome": 3,
    "Liberfarb_syndrome|PISD-related_mitochondrial_disease|not_provided": 1,
    "Liberfarb_syndrome|PISD-related_mitochondrial_disease": 1,
    "PISD-related_disorder|not_provided": 2,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_specified": 2,
    "not_provided|Familial_focal_epilepsy_with_variable_foci": 86,
    "Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci": 37,
    "Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 3,
    "Familial_focal_epilepsy_with_variable_foci|not_provided": 94,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 44,
    "Epilepsy|_familial_focal|_with_variable_foci_1": 102,
    "Familial_focal_epilepsy_with_variable_foci|DEPDC5-related_disorder": 7,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 2,
    "Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 22,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided|DEPDC5-related_disorder": 1,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided": 16,
    "DEPDC5-related_disorder|Inborn_genetic_diseases|not_provided|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 23,
    "Familial_focal_epilepsy_with_variable_foci|Seizure|not_provided": 1,
    "Familial_focal_epilepsy_with_variable_foci|not_provided|Inborn_genetic_diseases": 9,
    "DEPDC5-related_disorder": 18,
    "not_provided|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|not_specified|Epilepsy|_familial_focal|_with_variable_foci_1|Inborn_genetic_diseases": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 2,
    "Focal_epilepsy|Cortical_dysplasia": 1,
    "not_specified|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 1,
    "Seizure|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 1,
    "Familial_focal_epilepsy_with_variable_foci|not_provided|DEPDC5-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|not_specified": 1,
    "Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1|not_provided": 4,
    "Epilepsy|_familial_focal|_with_variable_foci_1|not_provided": 5,
    "Familial_focal_epilepsy_with_variable_foci|See_cases": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci|not_provided": 7,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 5,
    "Familial_focal_epilepsy_with_variable_foci|Developmental_and_epileptic_encephalopathy_111": 1,
    "Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1|Epileptic_encephalopathy|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Familial_focal_epilepsy_with_variable_foci": 1,
    "Epilepsy|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "not_specified|Familial_focal_epilepsy_with_variable_foci": 4,
    "Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Seizure": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|not_provided|Familial_focal_epilepsy_with_variable_foci": 2,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_1": 3,
    "Familial_focal_epilepsy_with_variable_foci|Self-limited_epilepsy_with_centrotemporal_spikes|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_1|not_provided|Familial_focal_epilepsy_with_variable_foci": 1,
    "Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 3,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Developmental_and_epileptic_encephalopathy_111|not_provided|Familial_focal_epilepsy_with_variable_foci": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci": 10,
    "Familial_focal_epilepsy_with_variable_foci|not_specified": 9,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_specified|not_provided": 5,
    "not_provided|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci": 2,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "not_provided|Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci": 10,
    "Inborn_genetic_diseases|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Developmental_and_epileptic_encephalopathy_111|Familial_focal_epilepsy_with_variable_foci": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|Intellectual_disability": 1,
    "Focal_epilepsy|Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci": 1,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 7,
    "Familial_focal_epilepsy_with_variable_foci|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|DEPDC5-related_disorder": 1,
    "Familial_focal_epilepsy_with_variable_foci|not_provided|Inborn_genetic_diseases|not_specified": 2,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|not_provided": 1,
    "Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 6,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|Familial_focal_epilepsy_with_variable_foci": 6,
    "not_specified|Intellectual_disability|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "not_provided|not_specified|Familial_focal_epilepsy_with_variable_foci": 1,
    "Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 2,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 2,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|not_provided": 3,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|Seizure|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_83|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_1|not_provided|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci": 1,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Seizure": 1,
    "not_provided|DEPDC5-related_disorder": 3,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|not_specified": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Developmental_and_epileptic_encephalopathy_111|Familial_focal_epilepsy_with_variable_foci": 2,
    "Focal_epilepsy|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "DEPDC5-related_disorder|Inborn_genetic_diseases|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|DEPDC5-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Familial_focal_epilepsy_with_variable_foci|DEPDC5-related_disorder": 1,
    "Inborn_genetic_diseases|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|not_specified|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 2,
    "Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1|Inborn_genetic_diseases": 1,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided|not_specified": 3,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Self-limited_epilepsy_with_centrotemporal_spikes|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|Focal_epilepsy|not_provided": 1,
    "not_specified|Familial_focal_epilepsy_with_variable_foci|not_provided": 1,
    "Familial_focal_epilepsy_with_variable_foci|not_specified|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Developmental_and_epileptic_encephalopathy_111|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy_111|not_provided|not_specified|Familial_focal_epilepsy_with_variable_foci": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|not_provided": 1,
    "Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci|not_specified|not_provided": 2,
    "See_cases|Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci": 1,
    "Intellectual_disability|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|See_cases": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "DEPDC5-related_disorder|Inborn_genetic_diseases|not_specified|Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy|Familial_focal_epilepsy_with_variable_foci|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_specified|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1": 2,
    "Familial_focal_epilepsy_with_variable_foci|Epilepsy": 1,
    "not_specified|Familial_focal_epilepsy_with_variable_foci|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|DEPDC5-related_disorder|not_provided|Familial_focal_epilepsy_with_variable_foci": 2,
    "DEPDC5-related_disorder|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 1,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Familial_focal_epilepsy_with_variable_foci|DEPDC5-related_disorder|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "DEPDC5-related_disorder|Inborn_genetic_diseases|Self-limited_epilepsy_with_centrotemporal_spikes|not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci": 1,
    "not_specified|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "not_provided|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|not_specified|Epilepsy|_familial_focal|_with_variable_foci_1|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 2,
    "not_provided|Epilepsy|_familial_focal|_with_variable_foci_1|not_specified|Familial_focal_epilepsy_with_variable_foci": 1,
    "not_provided|not_specified|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1|Seizure": 1,
    "Autosomal_dominant_epilepsy|Focal_epilepsy": 1,
    "Inborn_genetic_diseases|Familial_focal_epilepsy_with_variable_foci|not_provided|DEPDC5-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy_111|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Inborn_genetic_diseases|See_cases|Familial_focal_epilepsy_with_variable_foci|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "Epilepsy|_familial_focal|_with_variable_foci_1|DEPDC5-related_disorder|not_provided": 1,
    "Autosomal_dominant_epilepsy|Epilepsy|_familial_focal|_with_variable_foci_1": 1,
    "DEPDC5-related_disorder|Inborn_genetic_diseases": 1,
    "Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|Epilepsy|_familial_focal|_with_variable_foci_1|not_provided": 1,
    "not_specified|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Familial_focal_epilepsy_with_variable_foci|Autosomal_dominant_nocturnal_frontal_lobe_epilepsy": 1,
    "DEPDC5-related_disorder|Familial_focal_epilepsy_with_variable_foci|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Focal_epilepsy|not_provided": 1,
    "Congenital_glucose-galactose_malabsorption": 406,
    "Congenital_glucose-galactose_malabsorption|not_provided": 18,
    "Inborn_genetic_diseases|Congenital_glucose-galactose_malabsorption": 10,
    "not_specified|not_provided|Congenital_glucose-galactose_malabsorption": 2,
    "Congenital_glucose-galactose_malabsorption|SLC5A1-related_disorder": 3,
    "Inborn_genetic_diseases|Congenital_glucose-galactose_malabsorption|not_provided": 1,
    "not_provided|Congenital_glucose-galactose_malabsorption": 4,
    "SLC5A1-related_disorder|Congenital_glucose-galactose_malabsorption": 6,
    "SLC5A1-related_disorder": 3,
    "not_provided|SLC5A1-related_disorder|Congenital_glucose-galactose_malabsorption": 1,
    "Congenital_glucose-galactose_malabsorption|Inborn_genetic_diseases": 4,
    "SLC5A1-related_disorder|Inborn_genetic_diseases|Congenital_glucose-galactose_malabsorption": 1,
    "Renal_glycosuria": 1,
    "Congenital_glucose-galactose_malabsorption|not_specified|not_provided": 7,
    "Parkinsonian-pyramidal_syndrome|not_provided": 17,
    "Parkinsonian-pyramidal_syndrome": 300,
    "not_specified|not_provided|Parkinsonian-pyramidal_syndrome": 1,
    "FBXO7-related_disorder": 2,
    "not_provided|Parkinsonian-pyramidal_syndrome": 9,
    "Inborn_genetic_diseases|Parkinsonian-pyramidal_syndrome": 6,
    "Parkinsonian-pyramidal_syndrome|not_specified|not_provided": 1,
    "Parkinsonian-pyramidal_syndrome|FBXO7-related_disorder": 1,
    "Inborn_genetic_diseases|Parkinsonian-pyramidal_syndrome|not_provided": 2,
    "Parkinsonian-pyramidal_syndrome|not_provided|FBXO7-related_disorder|not_specified": 1,
    "Parkinsonian-pyramidal_syndrome|FBXO7-related_disorder|not_provided": 1,
    "Parkinsonian-pyramidal_syndrome|Inborn_genetic_diseases": 1,
    "Parkinsonian-pyramidal_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Parkinsonian-pyramidal_syndrome|Inborn_genetic_diseases": 1,
    "Parkinsonian-pyramidal_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Parkinsonian-pyramidal_syndrome": 1,
    "FBXO7-related_disorder|not_provided|Parkinsonian-pyramidal_syndrome": 1,
    "Global_developmental_delay|Cerebellar_vermis_atrophy|Generalized_hypotonia|Visual_impairment|Seizure": 1,
    "Fundus_dystrophy|_pseudoinflammatory|_recessive_form": 13,
    "Sorsby_fundus_dystrophy": 89,
    "Sorsby_fundus_dystrophy|not_provided": 14,
    "TIMP3-related_disorder|not_provided": 2,
    "not_provided|TIMP3-related_disorder": 2,
    "not_provided|not_specified|Sorsby_fundus_dystrophy": 1,
    "not_provided|SYN3-related_disorder": 1,
    "not_provided|Sorsby_fundus_dystrophy|Fundus_dystrophy|_pseudoinflammatory|_recessive_form|not_specified": 1,
    "not_provided|Sorsby_fundus_dystrophy": 7,
    "Sorsby_fundus_dystrophy|Retinal_dystrophy": 1,
    "TIMP3-related_disorder": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 35,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 20,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided": 2,
    "Walker-Warburg_congenital_muscular_dystrophy|Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 7,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6": 603,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 24,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6": 41,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided": 1,
    "LARGE1-related_disorder|Muscular_dystrophy-dystroglycanopathy_type_B6": 7,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6": 3,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6|not_specified": 2,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 5,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Inborn_genetic_diseases": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 7,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6": 12,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|LARGE1-related_disorder|not_specified": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|LARGE1-related_disorder|not_provided": 2,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 4,
    "LARGE1-related_disorder": 5,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 2,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|LARGE1-related_disorder": 7,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|not_specified": 2,
    "not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|LARGE1-related_disorder": 1,
    "LARGE1-related_disorder|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided|LARGE1-related_disorder|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 5,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 1,
    "LARGE1-Related_Disorders|Muscular_dystrophy-dystroglycanopathy_type_B6": 1,
    "LARGE1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided|not_specified": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided|LARGE1-related_disorder": 1,
    "LARGE1-related_disorder|not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6": 1,
    "Muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 1,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 2,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided|not_specified": 1,
    "not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 1,
    "LARGE1-related_disorder|not_specified|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "Muscular_dystrophy|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A1|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6|not_specified|not_provided": 2,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6|not_provided": 1,
    "LARGE1-related_disorder|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|Muscular_dystrophy-dystroglycanopathy_type_B6": 1,
    "not_provided|not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "Congenital_Muscular_Dystrophy|_alpha-dystroglycan_related|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6|not_provided|not_specified": 1,
    "not_specified|Muscular_dystrophy-dystroglycanopathy_type_B6|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "Immunodeficiency_85_and_autoimmunity|not_specified": 3,
    "Immunodeficiency_85_and_autoimmunity": 6,
    "HMOX1-related_disorder": 1,
    "Heme_oxygenase_1_deficiency": 3,
    "not_provided|Heme_oxygenase_1_deficiency": 3,
    "HMOX1-related_disorder|not_provided": 4,
    "not_provided|HMOX1-related_disorder": 3,
    "Heme_oxygenase_1_deficiency|not_provided|Chronic_obstructive_pulmonary_disease": 1,
    "not_provided|Heme_oxygenase_1_deficiency|COPD|_severe_early_onset|HMOX1-related_disorder": 1,
    "Heme_oxygenase_1_deficiency|not_provided": 1,
    "not_provided|MCM5-related_disorder": 6,
    "MCM5-related_disorder|not_provided": 5,
    "not_provided|Meier-Gorlin_syndrome_8": 2,
    "Meier-Gorlin_syndrome_8|not_provided": 1,
    "Meier-Gorlin_syndrome_8": 1,
    "MCM5-related_disorder": 1,
    "Myopathy|_sarcoplasmic_body|Colorectal_carcinoma": 1,
    "not_provided|Congenital_heart_defect": 1,
    "APOL1-related_disorder|not_provided": 5,
    "APOL1-related_disorder": 6,
    "not_provided|Focal_segmental_glomerulosclerosis_4|_susceptibility_to": 9,
    "not_specified|Focal_segmental_glomerulosclerosis_4|_susceptibility_to|not_provided": 2,
    "APOL1-related_disorder|not_provided|not_specified": 1,
    "Focal_segmental_glomerulosclerosis_4|_susceptibility_to|not_provided|APOL1-related_disorder": 2,
    "not_provided|Focal_segmental_glomerulosclerosis_4|_susceptibility_to|not_specified": 2,
    "not_specified|not_provided|APOL1-related_disorder": 4,
    "Focal_segmental_glomerulosclerosis_4|_susceptibility_to|not_provided": 4,
    "Focal_segmental_glomerulosclerosis_4|_susceptibility_to|Hyalinosis|_Segmental_Glomerular|not_specified|not_provided|Glomerulonephritis|APOL1-associated_kidney_disease|Proteinuria|Focal_segmental_glomerulosclerosis|Steroid-resistant_nephrotic_syndrome|Nephrotic_range_proteinuria|Sickled_erythrocytes": 1,
    "Nephrotic_range_proteinuria|Focal_segmental_glomerulosclerosis|Sickled_erythrocytes|Steroid-resistant_nephrotic_syndrome|APOL1-associated_kidney_disease|Hyalinosis|_Segmental_Glomerular|Glomerulonephritis|not_provided|Proteinuria|not_specified|Focal_segmental_glomerulosclerosis_4|_susceptibility_to": 1,
    "Focal_segmental_glomerulosclerosis_4|_susceptibility_to|not_specified|not_provided|Nephrotic_range_proteinuria|Focal_segmental_glomerulosclerosis|Hyalinosis|_Segmental_Glomerular": 1,
    "Nonsyndromic_Hearing_Loss|_Dominant|MYH9-related_disorder": 4,
    "MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17": 32,
    "not_provided|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17": 5,
    "MYH9-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 23,
    "MYH9-related_disorder|Nonsyndromic_Hearing_Loss|_Dominant": 4,
    "MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 10,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 20,
    "MYH9-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 17,
    "MYH9-related_disorder": 62,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Nephrotic_syndrome|not_provided|MYH9-related_disorder": 1,
    "MYH9-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 84,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 11,
    "not_provided|Inborn_genetic_diseases|MYH9-related_disorder": 4,
    "not_specified|MYH9-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 3,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|Focal_segmental_glomerulosclerosis|not_specified|MYH9-related_disorder": 1,
    "MYH9-related_disorder|not_provided|Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Thrombocytopenia|Abnormal_bleeding|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_provided": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 8,
    "not_provided|MYH9-related_disorder": 33,
    "not_provided|not_specified|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_specified|MYH9-related_disorder|Atypical_hemolytic-uremic_syndrome|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|not_provided": 21,
    "MYH9-related_disorder|Nonsyndromic_Hearing_Loss|_Dominant|Atypical_hemolytic-uremic_syndrome|not_specified|not_provided": 1,
    "MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|not_specified": 1,
    "MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 2,
    "not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 2,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 5,
    "not_specified|MYH9-related_disorder|not_provided": 3,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_provided": 2,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 14,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 27,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified|not_provided": 4,
    "not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 18,
    "Deafness|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "MYH9-related_disorder|not_specified|not_provided": 2,
    "not_provided|not_specified|MYH9-related_disorder": 3,
    "MYH9-related_disorder|not_provided|Kidney_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|Inborn_genetic_diseases|not_provided|Homocystinuria_due_to_methylene_tetrahydrofolate_reductase_deficiency|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Inborn_genetic_diseases|not_provided": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified|Nephrotic_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 1,
    "Capillary_infantile_hemangioma|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|not_provided": 6,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|Glomerulonephritis": 1,
    "Type_1_diabetes_mellitus_17": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|not_specified": 9,
    "not_provided|MYH9-related_disorder|not_specified": 4,
    "MYH9-related_disorder|Kidney_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 2,
    "Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|MYH9-related_disorder": 1,
    "MYH9-related_disorder|not_provided|not_specified": 3,
    "not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Inborn_genetic_diseases": 1,
    "Macrothrombocytopenia|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_provided": 1,
    "not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 2,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|Inborn_genetic_diseases": 1,
    "MYH9-related_disorder|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Hearing_impairment": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|not_specified|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Inborn_genetic_diseases": 4,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 24,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 6,
    "not_specified|Focal_segmental_glomerulosclerosis|MYH9-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|Thrombocytopenia": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 10,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|not_specified": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|not_specified|MYH9-related_disorder": 1,
    "not_specified|not_provided|Proteinuria|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 2,
    "Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_specified|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "not_provided|not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 2,
    "MYH9-related_disorder|not_specified|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|Inborn_genetic_diseases": 1,
    "Rare_genetic_deafness|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified": 2,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 4,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 1,
    "Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 2,
    "Inborn_genetic_diseases|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "Focal_segmental_glomerulosclerosis|Nephrotic_syndrome": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|MYH9-related_disorder": 1,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder": 3,
    "Numerous_pigmented_freckles|Hypertensive_disorder|Abnormal_platelet_function|Abnormal_platelet_morphology|Increased_mean_platelet_volume|Abnormal_platelet_shape|Thrombocytopenia|Obesity|Abnormal_facial_shape|Epistaxis|MYH9-related_disorder": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|MYH9-related_disorder": 2,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Thrombocytopenia": 1,
    "MYH9-related_disorder|Macrothrombocytopenia": 1,
    "not_specified|not_provided|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|Meniere_disease|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|Meniere_disease|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "MYH9-related_disorder|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|MYH9-related_disorder": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 3,
    "not_provided|MYH9-related_disorder|Focal_segmental_glomerulosclerosis|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified": 1,
    "not_provided|MYH9-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 4,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17": 4,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_provided": 1,
    "not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 1,
    "Inborn_genetic_diseases|Thrombocytopenia|Abnormal_bleeding|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|MYH9-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|not_provided|Atypical_hemolytic-uremic_syndrome|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|Nephrotic_syndrome|MYH9-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 1,
    "not_specified|not_provided|MYH9-related_disorder": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_specified|not_provided|Kidney_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "Thrombocytopenia|MYH9-related_disorder": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|MYH9-related_disorder": 1,
    "not_provided|Nonsyndromic_Hearing_Loss|_Dominant|MYH9-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "Inborn_genetic_diseases|MYH9-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|not_provided": 4,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Macrothrombocytopenia": 1,
    "not_specified|MYH9-related_disorder|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified|not_provided|MYH9-related_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided|not_specified": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|MYH9-related_disorder": 2,
    "MYH9-related_disorder|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|Kidney_disorder": 1,
    "Inborn_genetic_diseases|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified": 1,
    "Kidney_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "not_provided|MYH9-related_disorder|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Kidney_disorder": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|Atypical_hemolytic-uremic_syndrome|not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|MYH9-related_disorder|not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Inborn_genetic_diseases": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|not_provided|not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "Inborn_genetic_diseases|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder": 1,
    "not_provided|MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "not_specified|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided": 2,
    "not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified": 2,
    "MYH9-related_disorder|not_specified|Atypical_hemolytic-uremic_syndrome|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "not_specified|not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|Atypical_hemolytic-uremic_syndrome": 1,
    "not_specified|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|not_provided": 2,
    "not_provided|Severe_X-linked_myotubular_myopathy": 30,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|MYH9-related_disorder": 1,
    "not_specified|not_provided|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_specified|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|MYH9-related_disorder|not_specified": 1,
    "not_provided|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified": 2,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "MYH9-related_disorder|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_provided": 1,
    "Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_provided|not_specified": 1,
    "Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|Thrombocytopenia": 1,
    "not_provided|MYH9-related_disorder|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss": 1,
    "Vitelliform_macular_dystrophy_1|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|MYH9-related_disorder|not_specified|not_provided": 1,
    "May-Hegglin_Disorder": 1,
    "not_provided|Cataract_35": 1,
    "not_provided|Autosomal_dominant_nonsyndromic_hearing_loss_17|not_specified|MYH9-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Autosomal_dominant_nonsyndromic_hearing_loss_17|Macrothrombocytopenia_and_granulocyte_inclusions_with_or_without_nephritis_or_sensorineural_hearing_loss|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|MYH9-related_disorder": 1,
    "Combined_oxidative_phosphorylation_deficiency_29|not_provided": 1,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_deficiency_29": 1,
    "not_provided|TXN2-related_disorder|Combined_oxidative_phosphorylation_deficiency_29": 1,
    "not_provided|TXN2-related_disorder": 2,
    "Combined_oxidative_phosphorylation_deficiency_29": 1,
    "Intellectual_disability|_autosomal_dominant_10": 7,
    "CACNG2-related_disorder|not_provided|not_specified": 1,
    "Complex_neurodevelopmental_disorder|Intellectual_disability|_autosomal_dominant_10": 1,
    "CACNG2-related_disorder|not_provided": 1,
    "Intellectual_disability|_autosomal_dominant_10|not_specified": 1,
    "not_specified|Intellectual_disability|_autosomal_dominant_10": 1,
    "CACNG2-related_disorder": 1,
    "IFT27-related_disorder": 12,
    "IFT27-related_disorder|not_provided": 7,
    "IFT27-related_disorder|Inborn_genetic_diseases|not_provided": 5,
    "not_provided|IFT27-related_disorder": 14,
    "Inborn_genetic_diseases|IFT27-related_disorder|Optic_atrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|IFT27-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|IFT27-related_disorder": 3,
    "Bardet-Biedl_syndrome_19|not_provided|Bardet-Biedl_syndrome|IFT27-related_disorder": 1,
    "IFT27-related_disorder|Retinal_dystrophy|not_provided": 1,
    "not_provided|IFT27-related_disorder|Bardet-Biedl_syndrome": 1,
    "IFT27-related_disorder|Bardet-Biedl_syndrome_19": 1,
    "Bardet-Biedl_syndrome_19": 2,
    "not_provided|Bardet-Biedl_syndrome_19": 2,
    "IFT27-related_disorder|not_specified|not_provided": 1,
    "Bardet-Biedl_syndrome_19|not_provided": 1,
    "Bardet-Biedl_syndrome_19|not_provided|Bardet-Biedl_syndrome": 1,
    "IFT27-related_disorder|Retinal_dystrophy": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 266,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 20,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_provided": 7,
    "not_specified|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 4,
    "NCF4-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_provided": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_specified": 14,
    "not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 3,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 3,
    "NCF4-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_provided|not_specified": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_specified|not_provided": 5,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|NCF4-related_disorder": 3,
    "NCF4-related_disorder|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 2,
    "NCF4-related_disorder|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 1,
    "not_specified|NCF4-related_disorder|not_provided|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3": 1,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_provided|not_specified": 2,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|NCF4-related_disorder": 1,
    "not_specified|Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|not_provided": 2,
    "Granulomatous_disease|_chronic|_autosomal_recessive|_cytochrome_b-positive|_type_3|Chronic_granulomatous_disease": 1,
    "not_provided|NCF4-related_disorder": 1,
    "NCF4-related_disorder": 1,
    "not_provided|CSF2RB-related_disorder": 14,
    "Inborn_genetic_diseases|Surfactant_metabolism_dysfunction|_pulmonary|_5|not_provided": 1,
    "CSF2RB-related_disorder|not_provided": 10,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_5": 4,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_5|Inborn_genetic_diseases": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_5": 4,
    "Surfactant_metabolism_dysfunction|_pulmonary|_5|not_provided": 4,
    "CSF2RB-related_disorder": 2,
    "not_provided|CSF2RB-related_disorder|Inborn_genetic_diseases": 1,
    "CSF2RB-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_5|CSF2RB-related_disorder|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_5|CSF2RB-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|CSF2RB-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_5": 1,
    "MPST-related_disorder": 1,
    "Encephalopathy_due_to_beta-mercaptolactate-cysteine_disulfiduria": 1,
    "Myoclonic_dystonia_26": 101,
    "not_provided|Myoclonic_dystonia_26|KCTD17-related_disorder": 3,
    "Myoclonic_dystonia_26|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Myoclonic_dystonia_26": 6,
    "KCTD17-related_disorder": 1,
    "not_provided|Myoclonic_dystonia_26": 5,
    "Myoclonic_dystonia_26|not_provided": 4,
    "Myoclonic_dystonia_26|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Myoclonic_dystonia_26|Inborn_genetic_diseases": 1,
    "not_specified|Myoclonic_dystonia_26": 1,
    "not_provided|Inborn_genetic_diseases|Myoclonic_dystonia_26": 1,
    "Myoclonic_dystonia_26|not_specified": 1,
    "KCTD17-related_disorder|Myoclonic_dystonia_26|not_provided": 1,
    "Microcytic_anemia|not_provided": 22,
    "Microcytic_anemia": 41,
    "not_provided|Microcytic_anemia": 9,
    "not_specified|not_provided|Microcytic_anemia": 1,
    "not_provided|Microcytic_anemia|Inborn_genetic_diseases": 2,
    "Iron-refractory_iron_deficiency_anemia|Microcytic_anemia|not_provided|not_specified": 1,
    "not_specified|Microcytic_anemia|not_provided|Iron-refractory_iron_deficiency_anemia": 2,
    "TMPRSS6-related_disorder": 11,
    "Microcytic_anemia|not_provided|TMPRSS6-related_disorder": 2,
    "TMPRSS6-related_disorder|not_provided|Microcytic_anemia": 1,
    "Inborn_genetic_diseases|Microcytic_anemia": 4,
    "Microcytic_anemia|not_provided|Iron-refractory_iron_deficiency_anemia": 1,
    "TMPRSS6-related_disorder|not_provided": 3,
    "not_specified|Microcytic_anemia|not_provided": 4,
    "not_provided|Iron-refractory_iron_deficiency_anemia": 6,
    "Microcytic_anemia|Iron-refractory_iron_deficiency_anemia|not_provided": 1,
    "Microcytic_anemia|TMPRSS6-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Iron-refractory_iron_deficiency_anemia": 1,
    "Iron-refractory_iron_deficiency_anemia|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Microcytic_anemia": 1,
    "Microcytic_anemia|Iron-refractory_iron_deficiency_anemia|TMPRSS6-related_disorder": 1,
    "Microcytic_anemia|not_provided|Inborn_genetic_diseases": 1,
    "Microcytic_anemia|not_provided|not_specified": 1,
    "Iron-refractory_iron_deficiency_anemia|not_specified|Microcytic_anemia|not_provided": 1,
    "Iron-refractory_iron_deficiency_anemia|not_provided|TMPRSS6-related_disorder": 1,
    "Iron-refractory_iron_deficiency_anemia|not_provided|Inborn_genetic_diseases": 1,
    "Microcytic_anemia|TMPRSS6-related_disorder": 1,
    "not_provided|TMPRSS6-related_disorder": 1,
    "Microcytic_anemia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Iron-refractory_iron_deficiency_anemia": 1,
    "not_provided|Microcytic_anemia|Iron-refractory_iron_deficiency_anemia|not_specified": 1,
    "TMPRSS6-related_disorder|Microcytic_anemia|not_provided|Iron-refractory_iron_deficiency_anemia": 1,
    "not_provided|Iron-refractory_iron_deficiency_anemia|TMPRSS6-related_disorder": 1,
    "Iron-refractory_iron_deficiency_anemia|Microcytic_anemia": 1,
    "Inborn_genetic_diseases|not_provided|TMPRSS6-related_disorder|Microcytic_anemia": 1,
    "Inborn_genetic_diseases|TMPRSS6-related_disorder|not_provided": 1,
    "not_provided|TMPRSS6-related_disorder|Microcytic_anemia": 1,
    "not_specified|Microcytic_anemia|Iron-refractory_iron_deficiency_anemia|not_provided": 1,
    "IL2RB-related_disorder|not_provided": 7,
    "not_provided|IL2RB-related_disorder": 7,
    "IL2RB-related_disorder|not_specified|not_provided": 1,
    "Immunodeficiency_63_with_lymphoproliferation_and_autoimmunity": 5,
    "IL2RB-related_disorder": 1,
    "IL2RB-related_disorder|not_specified|not_provided|Immunodeficiency_63_with_lymphoproliferation_and_autoimmunity": 1,
    "Immunodeficiency_63_with_lymphoproliferation_and_autoimmunity|not_provided": 2,
    "Immunodeficiency_63_with_lymphoproliferation_and_autoimmunity|IL2RB-related_disorder|not_provided": 1,
    "not_specified|not_provided|IL2RB-related_disorder": 1,
    "not_provided|not_specified|Immunodeficiency_63_with_lymphoproliferation_and_autoimmunity": 1,
    "not_specified|Immunodeficiency_63_with_lymphoproliferation_and_autoimmunity|not_provided": 1,
    "Neutrophil_immunodeficiency_syndrome": 148,
    "Inborn_genetic_diseases|Neutrophil_immunodeficiency_syndrome": 1,
    "Neutrophil_immunodeficiency_syndrome|not_provided": 2,
    "Neutrophil_immunodeficiency_syndrome|Inborn_genetic_diseases": 3,
    "not_provided|Neutrophil_immunodeficiency_syndrome": 2,
    "Neutrophil_immunodeficiency_syndrome|Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia": 1,
    "not_provided|RAC2-related_disorder|Neutrophil_immunodeficiency_syndrome": 1,
    "Neutrophil_immunodeficiency_syndrome|not_specified|not_provided": 2,
    "RAC2-related_disorder": 2,
    "Neutrophil_immunodeficiency_syndrome|not_specified": 2,
    "not_provided|Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia|not_specified|Neutrophil_immunodeficiency_syndrome": 1,
    "not_provided|Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia|Neutrophil_immunodeficiency_syndrome|not_specified": 1,
    "RAC2-related_disorder|Neutrophil_immunodeficiency_syndrome": 1,
    "Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia": 3,
    "not_provided|Neutrophil_immunodeficiency_syndrome|not_specified": 1,
    "not_provided|Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia|Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|not_specified|Neutrophil_immunodeficiency_syndrome": 1,
    "Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|Neutrophil_immunodeficiency_syndrome|Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia|not_provided": 1,
    "Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia": 1,
    "Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|Neutrophil_immunodeficiency_syndrome": 1,
    "Neutrophil_immunodeficiency_syndrome|not_specified|Immunodeficiency_73b_with_defective_neutrophil_chemotaxis_and_lymphopenia|Immunodeficiency_73c_with_defective_neutrophil_chemotaxis_and_hypogammaglobulinemia|not_provided": 1,
    "Neutrophil_immunodeficiency_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Neutrophil_immunodeficiency_syndrome": 1,
    "CARD10-related_disorder": 25,
    "not_provided|CARD10-related_disorder": 3,
    "Immunodeficiency_89_and_autoimmunity|not_specified": 1,
    "Immunodeficiency_89_and_autoimmunity": 2,
    "CARD10-related_disorder|not_provided": 2,
    "CARD10-related_disorder|not_specified": 1,
    "LGALS2-related_disorder": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_28|not_provided": 3,
    "TRIOBP-related_disorder|not_specified": 2,
    "Autosomal_recessive_nonsyndromic_hearing_loss_28|not_provided": 14,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 20,
    "not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 2,
    "not_provided|not_specified|TRIOBP-related_disorder": 7,
    "TRIOBP-related_disorder|not_provided": 9,
    "TRIOBP-related_disorder|Inborn_genetic_diseases": 1,
    "TRIOBP-related_disorder|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 4,
    "not_provided|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_28": 5,
    "TRIOBP-related_disorder|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 3,
    "Autosomal_recessive_nonsyndromic_hearing_loss_28|not_provided|not_specified": 5,
    "TRIOBP-related_disorder": 13,
    "Autosomal_recessive_nonsyndromic_hearing_loss_28|not_provided|TRIOBP-related_disorder": 1,
    "TRIOBP-related_disorder|not_specified|not_provided": 2,
    "Rare_genetic_deafness|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "not_provided|TRIOBP-related_disorder": 14,
    "Nonsyndromic_genetic_hearing_loss|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "TRIOBP-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_28|TRIOBP-related_disorder|not_provided": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_28|TRIOBP-related_disorder": 1,
    "Autosomal_recessive_nonsyndromic_hearing_loss_28|Rare_genetic_deafness|not_provided": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28|Hearing_loss|_autosomal_recessive": 1,
    "Hearing_loss|_autosomal_recessive|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28|not_specified": 4,
    "Inborn_genetic_diseases|not_provided|TRIOBP-related_disorder": 1,
    "TRIOBP-related_disorder|Deafness|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "TRIOBP-related_disorder|not_provided|not_specified": 1,
    "not_specified|not_provided|TRIOBP-related_disorder": 3,
    "not_provided|TRIOBP-related_disorder|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "Meniere_disease|Autosomal_recessive_nonsyndromic_hearing_loss_28|Hearing_impairment|not_provided|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|TRIOBP-related_disorder": 1,
    "TRIOBP-related_disorder|Meniere_disease|not_specified|not_provided": 1,
    "TRIOBP-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28": 1,
    "Inborn_genetic_diseases|TRIOBP-related_hearing_loss": 1,
    "not_provided|TRIOBP-related_disorder|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|Autosomal_recessive_nonsyndromic_hearing_loss_28": 2,
    "not_specified|not_provided|Hearing_loss|_autosomal_recessive|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|TRIOBP-related_disorder": 1,
    "not_provided|Autosomal_recessive_nonsyndromic_hearing_loss_28|TRIOBP-related_disorder": 1,
    "TRIOBP-related_disorder|not_specified|Autosomal_recessive_nonsyndromic_hearing_loss_28|not_provided": 1,
    "PCWH_syndrome|Waardenburg_syndrome": 11,
    "Waardenburg_syndrome|PCWH_syndrome": 9,
    "PCWH_syndrome|Waardenburg_syndrome|not_provided": 3,
    "PCWH_syndrome": 16,
    "Waardenburg_syndrome_type_2E": 31,
    "SOX10-related_disorder": 14,
    "Waardenburg_syndrome_type_4C": 87,
    "Waardenburg_syndrome_type_2E|Waardenburg_syndrome_type_4C|PCWH_syndrome|not_provided": 1,
    "SOX10-related_disorder|not_provided": 7,
    "Waardenburg_syndrome|not_provided|PCWH_syndrome": 2,
    "not_provided|Waardenburg_syndrome_type_2E": 5,
    "not_provided|PCWH_syndrome": 4,
    "not_provided|Waardenburg_syndrome_type_2E|_with_neurologic_involvement|Waardenburg_syndrome_type_4C": 1,
    "not_provided|Waardenburg_syndrome|PCWH_syndrome": 3,
    "Waardenburg_syndrome_type_4C|not_provided": 7,
    "PCWH_syndrome|Waardenburg_syndrome_type_2E|Waardenburg_syndrome_type_4C|not_provided": 1,
    "not_provided|SOX10-related_disorder": 3,
    "not_provided|Waardenburg_syndrome_type_4C": 5,
    "not_provided|Waardenburg_syndrome_type_2E|PCWH_syndrome|Waardenburg_syndrome_type_4C|not_specified|Waardenburg_syndrome": 1,
    "Waardenburg_syndrome_type_2E|PCWH_syndrome|Waardenburg_syndrome_type_4C|not_specified|not_provided|Waardenburg_syndrome": 1,
    "Waardenburg_syndrome|PCWH_syndrome|not_provided": 1,
    "PCWH_syndrome|SOX10-related_disorder|Waardenburg_syndrome|not_specified": 1,
    "not_provided|PCWH_syndrome|SOX10-related_disorder|not_specified|Waardenburg_syndrome": 1,
    "Charcot-Marie-Tooth_disease|PCWH_syndrome": 1,
    "not_specified|not_provided|SOX10-related_disorder": 2,
    "Waardenburg_syndrome_type_4C|Waardenburg_syndrome_type_2E|PCWH_syndrome|not_provided": 1,
    "PCWH_syndrome|Waardenburg_syndrome|not_provided|not_specified": 2,
    "Waardenburg_syndrome_type_2E|_without_neurologic_involvement": 7,
    "Waardenburg_syndrome_type_2E|_with_neurologic_involvement": 2,
    "SOX10-related_disorder|not_provided|Inborn_genetic_diseases|Waardenburg_syndrome_type_2E": 1,
    "Waardenburg_syndrome_type_4C|Waardenburg_syndrome_type_2E": 2,
    "Deafness_with_anatomical_inner_ear_anomalies|Hypogonadotropic_hypogonadism|Waardenburg_syndrome_type_4C|Waardenburg_syndrome_type_2E|PCWH_syndrome|not_provided": 1,
    "Waardenburg_syndrome_type_2E|Waardenburg_syndrome_type_4C": 1,
    "PCWH_syndrome|not_specified|not_provided|Waardenburg_syndrome": 2,
    "Waardenburg_syndrome_type_2E|not_provided": 1,
    "Rare_genetic_deafness|Waardenburg_syndrome_type_2E": 1,
    "PCWH_syndrome|Waardenburg_syndrome_type_4C": 1,
    "not_provided|Waardenburg_syndrome_type_4C|PCWH_syndrome|Waardenburg_syndrome_type_2E": 1,
    "Deafness_with_anatomical_inner_ear_anomalies": 1,
    "Waardenburg_syndrome_type_2E|PCWH_syndrome|Waardenburg_syndrome_type_4C": 1,
    "not_provided|SOX10-related_disorder|Waardenburg_syndrome_type_2E": 1,
    "not_specified|Waardenburg_syndrome|Hearing_impairment|SOX10-related_disorder|not_provided|PCWH_syndrome": 1,
    "Waardenburg_syndrome_type_1|PCWH_syndrome": 1,
    "PCWH_syndrome|not_provided|not_specified|Waardenburg_syndrome": 1,
    "PCWH_syndrome|not_provided|Waardenburg_syndrome_type_2E": 1,
    "Waardenburg_syndrome_type_2E|Waardenburg_syndrome_type_4C|not_specified|not_provided": 1,
    "SOX10-related_disorder|Waardenburg_syndrome|PCWH_syndrome|not_specified|not_provided": 1,
    "Waardenburg_syndrome_type_4C|SOX10-related_disorder|not_provided|Waardenburg_syndrome_type_2E": 1,
    "not_provided|Waardenburg_syndrome_type_4C|Hypogonadism_with_anosmia": 1,
    "SOX10-related_disorder|not_specified|not_provided": 1,
    "not_provided|Waardenburg_syndrome_type_2A|Waardenburg_syndrome_type_4C": 1,
    "SOX10-related_disorder|not_provided|Hirschsprung_disease|_susceptibility_to|_1": 1,
    "PICK1-related_disorder|not_provided": 1,
    "PICK1-related_disorder": 1,
    "PLA2G6-associated_neurodegeneration": 35,
    "not_provided|PLA2G6-associated_neurodegeneration": 7,
    "not_provided|Infantile_neuroaxonal_dystrophy": 36,
    "Infantile_neuroaxonal_dystrophy": 577,
    "PLA2G6-associated_neurodegeneration|not_specified|not_provided|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14": 1,
    "Iron_accumulation_in_brain": 12,
    "Infantile_neuroaxonal_dystrophy|not_provided": 26,
    "Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Iron_accumulation_in_brain|Autosomal_recessive_Parkinson_disease_14|not_provided": 1,
    "Autism|Seizure|PLA2G6-related_disorder|PLA2G6-associated_neurodegeneration|Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|not_provided|Neurodegeneration_with_brain_iron_accumulation|Iron_accumulation_in_brain|Abnormality_of_the_nervous_system": 1,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|not_provided": 1,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 2,
    "PLA2G6-associated_neurodegeneration|not_specified|not_provided|Infantile_neuroaxonal_dystrophy": 3,
    "Infantile_neuroaxonal_dystrophy|Iron_accumulation_in_brain": 4,
    "Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 4,
    "PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation": 1,
    "Infantile_neuroaxonal_dystrophy|not_provided|PLA2G6-associated_neurodegeneration": 4,
    "Inborn_genetic_diseases|not_provided|Infantile_neuroaxonal_dystrophy": 7,
    "Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 6,
    "Inborn_genetic_diseases|PLA2G6-associated_neurodegeneration|not_provided|Infantile_neuroaxonal_dystrophy": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation": 1,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 9,
    "not_specified|Infantile_neuroaxonal_dystrophy": 6,
    "PLA2G6-associated_neurodegeneration|Iron_accumulation_in_brain|not_specified|not_provided|Infantile_neuroaxonal_dystrophy": 1,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided": 1,
    "PLA2G6-associated_neurodegeneration|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided": 4,
    "not_provided|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B|Iron_accumulation_in_brain|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_2B|Neurodegeneration_with_brain_iron_accumulation|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|Iron_accumulation_in_brain|not_provided|Inborn_genetic_diseases|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Iron_accumulation_in_brain": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Inborn_genetic_diseases": 1,
    "not_provided|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Abnormal_brain_morphology|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Iron_accumulation_in_brain|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy": 1,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided|Iron_accumulation_in_brain": 2,
    "Iron_accumulation_in_brain|Neurodegeneration_with_brain_iron_accumulation|not_provided|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Infantile_neuroaxonal_dystrophy|Iron_accumulation_in_brain": 3,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Inborn_genetic_diseases": 2,
    "not_provided|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 4,
    "Infantile_neuroaxonal_dystrophy|Iron_accumulation_in_brain|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|not_specified": 5,
    "not_provided|Infantile_neuroaxonal_dystrophy|PLA2G6-related_disorder|Inborn_genetic_diseases": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Infantile_neuroaxonal_dystrophy": 6,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 4,
    "PLA2G6-associated_neurodegeneration|not_provided": 2,
    "not_provided|Iron_accumulation_in_brain|Infantile_neuroaxonal_dystrophy": 1,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14": 2,
    "PLA2G6-associated_neurodegeneration|not_specified": 2,
    "Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration|not_provided": 1,
    "Iron_accumulation_in_brain|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration|not_provided": 1,
    "not_provided|Abnormality_of_the_nervous_system|PLA2G6-associated_neurodegeneration|not_specified|Infantile_neuroaxonal_dystrophy": 1,
    "PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|not_provided|Neurodegeneration_with_brain_iron_accumulation|Karak_syndrome": 1,
    "Abnormality_of_the_nervous_system|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "PLA2G6-related_disorder": 1,
    "Infantile_neuroaxonal_dystrophy|not_provided|not_specified": 3,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|not_provided": 2,
    "Infantile_osteopetrosis_with_neuroaxonal_dysplasia|Inborn_genetic_diseases|PLA2G6-related_disorder|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided|Neurodegeneration_with_brain_iron_accumulation|Iron_accumulation_in_brain": 1,
    "Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Neurodegeneration_with_brain_iron_accumulation|not_provided|PLA2G6-associated_neurodegeneration": 1,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_specified": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation|not_provided": 1,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy": 3,
    "Infantile_neuroaxonal_dystrophy|not_specified|Iron_accumulation_in_brain": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "not_specified|Infantile_neuroaxonal_dystrophy|not_provided|PLA2G6-associated_neurodegeneration": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Iron_accumulation_in_brain": 1,
    "Iron_accumulation_in_brain|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration": 1,
    "not_provided|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 2,
    "Infantile_neuroaxonal_dystrophy|Abnormal_brain_morphology|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation|Iron_accumulation_in_brain|PLA2G6-associated_neurodegeneration": 1,
    "Congenital_cerebellar_hypoplasia|Microcephaly|Cerebellar_ataxia|Global_developmental_delay|Developmental_regression|not_provided|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 1,
    "PLA2G6-associated_neurodegeneration|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided|Iron_accumulation_in_brain": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B|not_provided|Iron_accumulation_in_brain|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 1,
    "not_provided|Iron_accumulation_in_brain|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|PLA2G6-associated_neurodegeneration": 1,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 1,
    "not_provided|Iron_accumulation_in_brain": 1,
    "not_specified|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy": 1,
    "not_specified|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|not_specified|Iron_accumulation_in_brain|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation|PLA2G6-related_disorder|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided": 1,
    "Infantile_neuroaxonal_dystrophy|Inborn_genetic_diseases": 8,
    "PLA2G6-associated_neurodegeneration|Iron_accumulation_in_brain": 1,
    "PLA2G6-related_disorder|Infantile_neuroaxonal_dystrophy": 2,
    "PLA2G6-associated_neurodegeneration|Iron_accumulation_in_brain|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Infantile_neuroaxonal_dystrophy|not_provided|Neurodegeneration_with_brain_iron_accumulation": 2,
    "Neurodegeneration_with_brain_iron_accumulation|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy": 5,
    "Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy": 1,
    "Autosomal_recessive_Parkinson_disease_14": 2,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Iron_accumulation_in_brain|not_provided": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy": 1,
    "Iron_accumulation_in_brain|Infantile_neuroaxonal_dystrophy": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Infantile_neuroaxonal_dystrophy|Inborn_genetic_diseases": 1,
    "PLA2G6-associated_neurodegeneration|Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|not_provided": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation": 1,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|Iron_accumulation_in_brain": 1,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 1,
    "not_specified|not_provided|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 1,
    "not_provided|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Infantile_neuroaxonal_dystrophy|not_specified|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 1,
    "PLA2G6-associated_neurodegeneration|Inborn_genetic_diseases|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|not_specified|not_provided|Iron_accumulation_in_brain": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation|not_provided": 1,
    "Vascular_parkinsonism|Parkinsonian_disorder|Parkinson_disease|Infantile_neuroaxonal_dystrophy": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B|not_provided": 1,
    "PLA2G6-related_disorder|PLA2G6-associated_neurodegeneration|Parkinson_disease|Parkinsonian_disorder|Vascular_parkinsonism|not_specified|not_provided|Infantile_neuroaxonal_dystrophy": 1,
    "not_provided|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|Inborn_genetic_diseases": 1,
    "not_provided|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration": 1,
    "not_specified|Iron_accumulation_in_brain": 1,
    "PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided": 2,
    "not_provided|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy": 2,
    "not_provided|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|not_specified": 1,
    "not_provided|not_specified|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration": 1,
    "Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B|not_specified": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy": 1,
    "Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|Infantile_neuroaxonal_dystrophy": 2,
    "Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided|Inborn_genetic_diseases": 1,
    "Autosomal_recessive_Parkinson_disease_14|not_provided": 1,
    "PLA2G6-associated_neurodegeneration|not_specified|Infantile_neuroaxonal_dystrophy": 1,
    "not_provided|PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation|Iron_accumulation_in_brain": 1,
    "PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation|Infantile_neuroaxonal_dystrophy": 1,
    "not_provided|Infantile_neuroaxonal_dystrophy|Iron_accumulation_in_brain": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Neurodegeneration_with_brain_iron_accumulation|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "not_provided|Infantile_neuroaxonal_dystrophy|not_specified": 1,
    "not_specified|not_provided|Infantile_neuroaxonal_dystrophy|Iron_accumulation_in_brain": 1,
    "Infantile_neuroaxonal_dystrophy|not_provided|PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 1,
    "Infantile_neuroaxonal_dystrophy|not_provided|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_specified|not_provided": 1,
    "Infantile_neuroaxonal_dystrophy|See_cases": 1,
    "not_specified|PLA2G6-associated_neurodegeneration|PLA2G6-related_disorder|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided": 1,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Neurodegeneration_with_brain_iron_accumulation|Iron_accumulation_in_brain|Inborn_genetic_diseases|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|not_provided": 1,
    "Infantile_neuroaxonal_dystrophy|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|Infantile_neuroaxonal_dystrophy|not_specified": 1,
    "not_provided|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14|PLA2G6-associated_neurodegeneration|not_provided": 1,
    "PLA2G6-associated_neurodegeneration|not_provided|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "not_specified|not_provided|Infantile_neuroaxonal_dystrophy": 2,
    "Infantile_neuroaxonal_dystrophy|not_specified|not_provided": 1,
    "Spastic_ataxia|not_provided|Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 1,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B": 1,
    "Neurodegeneration_with_brain_iron_accumulation_2B|Iron_accumulation_in_brain|Infantile_neuroaxonal_dystrophy|Autosomal_recessive_Parkinson_disease_14|not_provided|PLA2G6-associated_neurodegeneration": 1,
    "PLA2G6-associated_neurodegeneration|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided|not_specified": 1,
    "Infantile_neuroaxonal_dystrophy|PLA2G6-associated_neurodegeneration|Inborn_genetic_diseases|Autosomal_recessive_Parkinson_disease_14|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided": 1,
    "not_provided|not_specified|PLA2G6-associated_neurodegeneration|Infantile_neuroaxonal_dystrophy": 1,
    "Iron_accumulation_in_brain|Autosomal_recessive_Parkinson_disease_14|Infantile_neuroaxonal_dystrophy|Neurodegeneration_with_brain_iron_accumulation_2B|not_provided": 1,
    "not_provided|Autosomal_recessive_Parkinson_disease_14": 1,
    "Infantile_neuroaxonal_dystrophy|not_provided|PLA2G6-associated_neurodegeneration|Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_2B|Autosomal_recessive_Parkinson_disease_14": 1,
    "Cerebellar_ataxia|Decreased_response_to_growth_hormone_stimulation_test|Sacral_dimple|Cardiac_arrhythmia|Seizure|Abnormal_testis_morphology|Intellectual_disability|_moderate|Bradycardia|Abnormal_facial_shape|Hypotonia|Aplasia/Hypoplasia_of_the_macula|Delayed_speech_and_language_development": 1,
    "Neurodevelopmental_disorder_with_characteristic_facial_and_ectodermal_features_and_tetraparesis_1": 3,
    "not_provided|not_specified|Emery-Dreifuss_muscular_dystrophy": 2,
    "DNAL4-related_disorder": 1,
    "Mirror_movements_3": 1,
    "not_provided|APOBEC3B-related_condition": 1,
    "APOBEC3B-related_condition": 2,
    "not_specified|APOBEC3B-related_condition": 1,
    "PDGFB-related_disorder": 5,
    "Basal_ganglia_calcification|_idiopathic|_5": 9,
    "not_provided|Dermatofibrosarcoma_protuberans": 1,
    "Inborn_genetic_diseases|Idiopathic_basal_ganglia_calcification_1|Basal_ganglia_calcification|_idiopathic|_5|Familial_meningioma|not_provided": 1,
    "not_provided|not_specified|Dermatofibrosarcoma_protuberans": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_5": 1,
    "PDGFB-related_disorder|not_provided|not_specified": 1,
    "not_provided|Basal_ganglia_calcification|_idiopathic|_5|PDGFB-related_disorder": 1,
    "Basal_ganglia_calcification|_idiopathic|_5|not_provided": 2,
    "PDGFB-related_disorder|not_specified|not_provided": 1,
    "PDGFB-related_disorder|not_provided": 1,
    "Dermatofibrosarcoma_protuberans|not_provided": 1,
    "Optic_atrophy_14": 2,
    "CACNA1I-related_disorder": 53,
    "not_provided|CACNA1I-related_disorder": 12,
    "Neurodevelopmental_disorder_with_speech_impairment_and_with_or_without_seizures": 37,
    "Ventriculomegaly|Antenatal_intracerebral_hemorrhage": 1,
    "CACNA1I-related_disorder|not_provided": 7,
    "not_specified|CACNA1I-related_disorder": 2,
    "CACNA1I-related_disorder|not_specified": 1,
    "not_specified|Neurodevelopmental_disorder_with_speech_impairment_and_with_or_without_seizures": 1,
    "not_specified|Neurodevelopmental_disorder_with_speech_impairment_and_with_or_without_seizures|not_provided": 1,
    "Neurodevelopmental_disorder_with_speech_impairment_and_with_or_without_seizures|not_specified": 2,
    "not_provided|Neurodevelopmental_disorder_with_speech_impairment_and_with_or_without_seizures": 1,
    "Abnormal_sperm_morphology|Reduced_sperm_motility|Oligospermia|not_specified": 1,
    "not_provided|TNRC6B-related_disorder": 8,
    "Global_developmental_delay_with_speech_and_behavioral_abnormalities": 74,
    "TNRC6B-related_disorder": 39,
    "TNRC6B-related_disorder|not_provided": 4,
    "Global_developmental_delay_with_speech_and_behavioral_abnormalities|not_provided": 4,
    "TNRC6B-related_disorder|not_specified": 1,
    "TNRC6B-related_disorder|Inborn_genetic_diseases": 2,
    "Neurodevelopmental_disorder_with_dysmorphic_facies_and_distal_limb_anomalies|Global_developmental_delay_with_speech_and_behavioral_abnormalities": 1,
    "not_provided|Global_developmental_delay_with_speech_and_behavioral_abnormalities": 3,
    "Inborn_genetic_diseases|not_provided|Global_developmental_delay_with_speech_and_behavioral_abnormalities": 1,
    "Inborn_genetic_diseases|Global_developmental_delay_with_speech_and_behavioral_abnormalities": 3,
    "Neurodevelopmental_delay|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TNRC6B-related_disorder": 3,
    "Inborn_genetic_diseases|TNRC6B-related_disorder|not_provided": 1,
    "Atypical_behavior|Global_developmental_delay|Autistic_behavior": 2,
    "TNRC6B-related_complex_neurodevelopmental_disorder": 1,
    "TNRC6B-related_disorder|not_specified|Global_developmental_delay_with_speech_and_behavioral_abnormalities": 1,
    "Adenylosuccinate_lyase_deficiency": 667,
    "not_provided|Adenylosuccinate_lyase_deficiency": 36,
    "Inborn_genetic_diseases|Adenylosuccinate_lyase_deficiency": 3,
    "Adenylosuccinate_lyase_deficiency|not_specified": 9,
    "Adenylosuccinate_lyase_deficiency|not_provided": 32,
    "Adenylosuccinate_lyase_deficiency|Inborn_genetic_diseases": 6,
    "not_specified|Adenylosuccinate_lyase_deficiency": 9,
    "Adenylosuccinate_lyase_deficiency|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Adenylosuccinate_lyase_deficiency": 4,
    "ADSL-related_disorder": 2,
    "not_provided|not_specified|Adenylosuccinate_lyase_deficiency": 4,
    "Adenylosuccinate_lyase_deficiency|ADSL-related_disorder": 2,
    "Adenylosuccinate_lyase_deficiency|not_provided|not_specified": 3,
    "not_provided|Adenylosuccinate_lyase_deficiency|not_specified": 2,
    "Inborn_genetic_diseases|ADSL-related_disorder|not_provided|Adenylosuccinate_lyase_deficiency|Difficulty_standing|Inability_to_walk|Severe_global_developmental_delay|Generalized_myoclonic_seizure|Progressive_neurologic_deterioration": 1,
    "Adenylosuccinate_lyase_deficiency|not_specified|not_provided": 3,
    "not_specified|not_provided|Adenylosuccinate_lyase_deficiency": 2,
    "not_provided|Severe_global_developmental_delay|Generalized_myoclonic_seizure|Progressive_neurologic_deterioration|Inability_to_walk|Difficulty_standing|Adenylosuccinate_lyase_deficiency": 1,
    "ADSL-related_disorder|not_provided|Adenylosuccinate_lyase_deficiency": 1,
    "not_provided|Adenylosuccinate_lyase_deficiency|Inborn_genetic_diseases": 2,
    "ADSL-related_disorder|not_provided|not_specified|Adenylosuccinate_lyase_deficiency": 1,
    "not_specified|not_provided|ADSL-related_disorder|Adenylosuccinate_lyase_deficiency": 1,
    "not_specified|Adenylosuccinate_lyase_deficiency|not_provided": 1,
    "Adenylosuccinate_lyase_deficiency|ADSL-related_disorder|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Adenylosuccinate_lyase_deficiency": 1,
    "ADSL-related_disorder|Adenylosuccinate_lyase_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Adenylosuccinate_lyase_deficiency|not_provided": 1,
    "not_provided|Adenylosuccinate_lyase_deficiency|ADSL-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Adenylosuccinate_lyase_deficiency": 3,
    "Adenylosuccinate_lyase_deficiency|not_provided|ADSL-related_disorder": 1,
    "Adenylosuccinate_lyase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "SGSM3-related_intellectual_disability|not_provided": 1,
    "not_provided|MRTFA-related_disorder|not_specified": 3,
    "MRTFA-related_disorder|not_provided": 17,
    "Immunodeficiency_66|not_specified|not_provided": 4,
    "not_provided|MRTFA-related_disorder": 6,
    "not_provided|Immunodeficiency_66": 2,
    "Immunodeficiency_66": 2,
    "MRTFA-related_disorder|not_specified|not_provided": 2,
    "Immunodeficiency_66|not_provided": 2,
    "not_specified|Immunodeficiency_66|not_provided": 2,
    "not_specified|MRTFA-related_disorder|not_provided": 1,
    "MCHR1-related_disorder": 13,
    "not_specified|MCHR1-related_disorder": 4,
    "MCHR1-related_disorder|not_specified|not_provided": 1,
    "MCHR1-related_disorder|not_provided": 1,
    "not_provided|MCHR1-related_disorder": 1,
    "Nephronophthisis-Like_Nephropathy|Nephronophthisis-like_nephropathy_1": 1,
    "Nephronophthisis-Like_Nephropathy|not_provided": 2,
    "Nephronophthisis-Like_Nephropathy": 18,
    "Nephronophthisis-like_nephropathy_1": 242,
    "not_provided|Nephronophthisis-like_nephropathy_1": 16,
    "Nephronophthisis-like_nephropathy_1|Inborn_genetic_diseases": 14,
    "not_specified|Nephronophthisis-like_nephropathy_1|not_provided": 1,
    "Nephronophthisis-like_nephropathy_1|not_provided": 5,
    "Inborn_genetic_diseases|Nephronophthisis-like_nephropathy_1|not_provided": 1,
    "Nephronophthisis-like_nephropathy_1|XPNPEP3-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Nephronophthisis-like_nephropathy_1": 2,
    "Nephronophthisis-like_nephropathy_1|Kidney_disorder": 1,
    "not_provided|Nephronophthisis-like_nephropathy_1|not_specified": 1,
    "XPNPEP3-related_disorder|Nephronophthisis-like_nephropathy_1|Kidney_disorder|not_specified": 1,
    "EP300-related_disorder": 254,
    "Menke-Hennekam_syndrome_2": 17,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 688,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 90,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_2|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 3,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 37,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 89,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|EP300-related_disorder": 18,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 45,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|not_provided": 3,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_2|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|Neurodevelopmental_delay": 1,
    "EP300-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 4,
    "Autosomal_dominant_cerebellar_ataxia|EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases": 1,
    "EP300-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 17,
    "EP300-related_disorder|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 4,
    "not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 1,
    "EP300-related_disorder|Inborn_genetic_diseases": 5,
    "Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 4,
    "not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|Inborn_genetic_diseases": 1,
    "EP300-related_disorder|not_provided": 14,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases": 16,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|EP300-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|Colorectal_cancer|EP300-related_disorder|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified": 8,
    "Inborn_genetic_diseases|EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 10,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 13,
    "EP300-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|not_specified|not_provided": 1,
    "EP300-related_disorder|Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "not_specified|EP300-related_disorder": 2,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|not_specified|not_provided": 1,
    "Intellectual_disability|Inborn_genetic_diseases|not_provided|EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|EP300-related_disorder|not_provided": 1,
    "not_provided|EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 12,
    "not_provided|EP300-related_disorder": 15,
    "not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|EP300-related_disorder": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 8,
    "EP300-related_disorder|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 11,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_2|Colorectal_cancer|EP300-related_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Intellectual_disability|EP300-related_disorder|Inborn_genetic_diseases": 1,
    "Colorectal_carcinoma|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 6,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified": 4,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|Colorectal_cancer|EP300-related_disorder": 1,
    "not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 4,
    "not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 10,
    "not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 6,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|Inborn_genetic_diseases": 4,
    "EP300-related_disorder|Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 1,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer|Menke-Hennekam_syndrome_2": 1,
    "Menke-Hennekam_syndrome_2|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 2,
    "Rubinstein-Taybi_syndrome|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_2|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|not_specified|not_provided": 2,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Thumb_deformity|Facial_grimacing|Micrognathia|Feeding_difficulties": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Carcinoma_of_colon": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2": 5,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|Multicystic_kidney_dysplasia|EP300-related_disorder": 1,
    "not_specified|EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer": 3,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|not_specified": 3,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|not_provided": 10,
    "Corpus_callosum|_agenesis_of|Microcephaly|Epileptic_encephalopathy": 1,
    "Menke-Hennekam_syndrome_2|Intellectual_disability|_moderate|Primary_microcephaly|Synophrys|Hirsutism|Short_stature|Myopia|Hypotonia": 1,
    "not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases|EP300-related_disorder": 1,
    "not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "Microcephaly|intellectual_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "not_specified|EP300-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 2,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|Inborn_genetic_diseases": 3,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases|not_provided|EP300-related_disorder": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|EP300-related_disorder": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer": 1,
    "Inborn_genetic_diseases|EP300-related_disorder": 5,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Colorectal_cancer|Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|not_provided": 1,
    "not_provided|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|See_cases": 1,
    "EP300-related_disorder|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|See_cases": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|not_specified|EP300-related_disorder": 1,
    "Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|not_specified|not_provided": 1,
    "Abnormal_facial_shape|Intellectual_disability|Postaxial_polydactyly": 1,
    "EP300-related_disorder|not_provided|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Menke-Hennekam_syndrome_2|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Developmental_and_epileptic_encephalopathy|_18": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|Menke-Hennekam_syndrome_2": 1,
    "CHARGE_syndrome|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 2,
    "not_provided|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 2,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Inborn_genetic_diseases|EP300-related_disorder": 4,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer|Menke-Hennekam_syndrome_2": 1,
    "Atypical_Rubinstein-Taybi": 1,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 1,
    "Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified": 1,
    "not_provided|Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Intellectual_disability|See_cases|EP300-related_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|Colorectal_cancer|not_provided": 1,
    "Intellectual_disability|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|EP300-related_disorder|not_provided": 1,
    "EP300-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "not_provided|Hepatoblastoma|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|Menke-Hennekam_syndrome_2": 1,
    "Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 1,
    "EP300-related_disorder|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "not_provided|Hereditary_breast_ovarian_cancer_syndrome|EP300-related_disorder": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_carcinoma|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|EP300-related_disorder|Inborn_genetic_diseases|Multiple_congenital_anomalies": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Menke-Hennekam_syndrome_2|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|EP300-related_disorder|not_provided": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|Inborn_genetic_diseases": 1,
    "EP300-related_disorder|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Intellectual_disability": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_cancer|not_provided|Inborn_genetic_diseases": 1,
    "EP300-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 2,
    "not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder|not_provided": 2,
    "Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Menke-Hennekam_syndrome_2|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|EP300-related_disorder": 1,
    "EP300-related_disorder|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_specified|Inborn_genetic_diseases": 1,
    "EP300-related_disorder|Inborn_genetic_diseases|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|See_cases": 1,
    "not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2": 1,
    "Menke-Hennekam_syndrome_2|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "not_specified|EP300-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Inborn_genetic_diseases|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided|Inborn_genetic_diseases|EP300-related_disorder": 2,
    "EP300-related_disorder|not_provided|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations": 1,
    "Menke-Hennekam_syndrome_2|Colorectal_cancer|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|not_provided": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|EP300-related_disorder": 1,
    "EP300-related_disorder|Inborn_genetic_diseases|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Colorectal_carcinoma|EP300-related_disorder": 1,
    "EP300-related_disorder|not_provided|not_specified|Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency": 1,
    "Rubinstein-Taybi_syndrome_due_to_EP300_haploinsufficiency|Menke-Hennekam_syndrome_2|Rubinstein-Taybi_syndrome_due_to_CREBBP_mutations|Colorectal_cancer|EP300-related_disorder|not_provided": 1,
    "Optic_atrophy|Optic_atrophy_9": 1,
    "Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration": 1,
    "Optic_atrophy_9|Central_hypoventilation|Global_developmental_delay|Brain_atrophy|Progressive_microcephaly|Neurodegeneration": 1,
    "Optic_atrophy_9|Acute_intermittent_porphyria|Central_hypoventilation|Global_developmental_delay|Brain_atrophy|Progressive_microcephaly|Neurodegeneration": 1,
    "ACO2-related_disorder|not_provided": 5,
    "not_provided|Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration": 2,
    "Optic_atrophy_9|not_specified|Infantile_cerebellar-retinal_degeneration|not_provided": 1,
    "OPTIC_ATROPHY_9|_AUTOSOMAL_RECESSIVE|ACO2-related_disorder|Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration|Retinal_dystrophy|not_specified|not_provided|Optic_atrophy": 1,
    "Infantile_cerebellar-retinal_degeneration|not_provided": 6,
    "Optic_atrophy_9": 9,
    "not_provided|ACO2-related_disorder": 7,
    "ACO2-related_disorder|OPTIC_ATROPHY_9|_AUTOSOMAL_RECESSIVE|not_provided": 1,
    "Infantile_cerebellar-retinal_degeneration|not_provided|ACO2-related_disorder": 1,
    "not_provided|Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration|not_specified": 1,
    "not_provided|Infantile_cerebellar-retinal_degeneration": 5,
    "Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration|Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Mitochondrial_disease": 1,
    "Optic_atrophy_9|not_provided|Infantile_cerebellar-retinal_degeneration": 2,
    "Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration|not_provided|Isolated_macular_dystrophy": 1,
    "Infantile_cerebellar-retinal_degeneration|Optic_atrophy_9|not_provided": 1,
    "ACO2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Infantile_cerebellar-retinal_degeneration|not_provided|Optic_atrophy_9": 1,
    "not_provided|ACO2-related_disorder|Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration": 1,
    "Optic_atrophy_9|not_provided": 3,
    "not_provided|ACO2-related_disorder|Infantile_cerebellar-retinal_degeneration|Optic_atrophy_9": 1,
    "Global_developmental_delay|Central_hypoventilation|Progressive_microcephaly|Brain_atrophy|Neurodegeneration": 2,
    "ACO2-related_disorder": 4,
    "not_provided|Optic_atrophy_9": 2,
    "Mitochondrial_disease|Optic_atrophy_9": 1,
    "Inborn_genetic_diseases|ACO2-related_disorder|not_provided": 1,
    "OPTIC_ATROPHY_9|_AUTOSOMAL_RECESSIVE|not_provided": 1,
    "OPTIC_ATROPHY_9|_AUTOSOMAL_RECESSIVE|Optic_atrophy|not_provided": 1,
    "Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration|not_provided": 1,
    "Optic_atrophy_9|Infantile_cerebellar-retinal_degeneration|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Infantile_cerebellar-retinal_degeneration": 1,
    "Inborn_genetic_diseases|not_provided|ACO2-related_disorder": 1,
    "Infantile_cerebellar-retinal_degeneration|Optic_atrophy": 1,
    "MEI1-related_disorder": 29,
    "MEI1-related_disorder|not_provided": 5,
    "Hydatidiform_mole|_recurrent|_3": 7,
    "not_provided|MEI1-related_disorder": 1,
    "MEI1-related_disorder|Hydatidiform_mole|_recurrent|_3": 1,
    "Severe_progressive_deforming_recessive_osteogenesis_imperfecta_(type_III)|Osteogenesis_imperfecta|_IIA_22|Recurrent_fractures": 1,
    "Osteogenesis_imperfecta|_IIA_22|not_specified": 1,
    "not_specified|CCDC134-related_condition": 1,
    "Osteogenesis_imperfecta|_IIA_22": 1,
    "SREBF2-related_disorder": 14,
    "SREBF2-related_disorder|not_provided": 2,
    "not_provided|SREBF2-related_disorder": 1,
    "Immunodeficiency|_common_variable|_4": 153,
    "not_provided|Immunodeficiency|_common_variable|_4": 3,
    "TNFRSF13C-related_disorder": 1,
    "not_specified|Immunodeficiency|_common_variable|_4": 3,
    "Immunodeficiency|_common_variable|_4|not_provided": 4,
    "Immunodeficiency|_common_variable|_4|not_specified": 4,
    "not_provided|Immunodeficiency|_common_variable|_4|Immunodeficiency|_common_variable|_2|not_specified": 1,
    "Immunodeficiency|_common_variable|_4|TNFRSF13C-related_disorder": 1,
    "Common_Variable_Immune_Deficiency|_Recessive|Immunodeficiency|_common_variable|_4": 1,
    "TNFRSF13C-related_disorder|Immunodeficiency|_common_variable|_4": 1,
    "TNFRSF13C-related_disorder|Immunodeficiency|_common_variable|_4|not_provided": 1,
    "TNFRSF13C-related_disorder|not_provided|Immunodeficiency|_common_variable|_4": 2,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency_type_1|not_provided": 7,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 8,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 32,
    "not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2": 13,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1": 249,
    "Inborn_genetic_diseases|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 4,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|NAGA-related_disorder|not_specified": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency_type_1|not_specified": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency|NAGA-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2|See_cases|Intellectual_disability": 1,
    "NAGA-related_disorder|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "Inborn_genetic_diseases|NAGA-related_disorder|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|not_provided": 2,
    "Alpha-N-acetylgalactosaminidase_deficiency|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|Inborn_genetic_diseases": 1,
    "not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 4,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|not_specified|Intellectual_disability": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|Inborn_genetic_diseases|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "not_provided|not_specified|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_3": 1,
    "not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2|Inborn_genetic_diseases": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency|Alpha-N-acetylgalactosaminidase_deficiency_type_1|not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_2|Alpha-N-acetylgalactosaminidase_deficiency_type_3|not_specified": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|not_specified|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "not_specified|not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_1": 1,
    "NAGA-related_disorder|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2": 1,
    "NAGA-related_disorder|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2|not_provided": 2,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_1|Alpha-N-acetylgalactosaminidase_deficiency_type_2|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Alpha-N-acetylgalactosaminidase_deficiency_type_1|not_specified": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency_type_2|not_provided|Alpha-N-acetylgalactosaminidase_deficiency_type_1|Inborn_genetic_diseases": 1,
    "Alpha-N-acetylgalactosaminidase_deficiency": 1,
    "NAGA-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_33": 1,
    "NDUFA6-related_disorder|not_provided": 3,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_33": 1,
    "Mitochondrial_disease|Mitochondrial_complex_I_deficiency|_nuclear_type_33": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_33|Mitochondrial_disease": 3,
    "Inborn_genetic_diseases|Mitochondrial_disease|Mitochondrial_complex_I_deficiency|_nuclear_type_33|NDUFA6-related_disorder": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_33|NDUFA6-related_disorder": 1,
    "not_provided|NDUFA6-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|NDUFA6-related_disorder": 1,
    "NDUFA6-related_disorder": 1,
    "not_specified|not_provided|Tramadol_response": 2,
    "CYP2D6-related_condition": 1,
    "not_provided|Tramadol_response|Tamoxifen_response|Deutetrabenazine_response": 1,
    "not_provided|not_specified|Tramadol_response": 1,
    "not_provided|Debrisoquine|_poor_metabolism_of": 2,
    "not_provided|not_specified|Debrisoquine|_poor_metabolism_of|Tramadol_response|Tamoxifen_response|Deutetrabenazine_response": 1,
    "not_provided|Debrisoquine|_poor_metabolism_of|Tamoxifen_response|Deutetrabenazine_response": 1,
    "not_specified|not_provided|Debrisoquine|_poor_metabolism_of|Tramadol_response|Tamoxifen_response|Deutetrabenazine_response": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities": 113,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|not_provided": 17,
    "TCF20-related_disorder": 19,
    "not_provided|TCF20-related_disorder": 10,
    "TCF20-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "TCF20-related_disorder|not_provided": 18,
    "Neurodevelopmental_abnormality|Attention_deficit_hyperactivity_disorder|Hypotonia|Neurodevelopmental_delay|Autistic_behavior": 1,
    "not_provided|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities": 8,
    "not_provided|Inborn_genetic_diseases|TCF20-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|not_provided": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|not_provided|Inborn_genetic_diseases": 2,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|Inborn_genetic_diseases": 2,
    "TCF20-related_neurodevelopmental_disorder": 1,
    "Hypotelorism|Intellectual_disability|Generalized_hypotonia": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|not_provided|Neurodevelopmental_abnormality": 3,
    "not_provided|TCF20-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities": 5,
    "Inborn_genetic_diseases|not_provided|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities": 2,
    "TCF20-related_disorder|Intellectual_disability": 1,
    "Pectus_excavatum|Intellectual_disability|_moderate|Generalized_hypotonia|Failure_to_thrive|Ptosis": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|TCF20-related_disorder|not_provided": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|Intellectual_disability|_mild|Myoclonus|Autism": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|not_provided|Inborn_genetic_diseases|Neurodevelopmental_abnormality|Neurodevelopmental_delay": 1,
    "not_provided|TCF20-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|TCF20-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability|_mild|Autism": 1,
    "TCF20-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|Neurodevelopmental_abnormality|not_provided": 1,
    "not_provided|Neurodevelopmental_abnormality|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities": 1,
    "not_specified|Developmental_delay_with_variable_intellectual_impairment_and_behavioral_abnormalities|TCF20-related_disorder|not_provided": 1,
    "Microcephaly_28|_primary|_autosomal_recessive": 1,
    "Craniosynostosis-anal_anomalies-porokeratosis_syndrome": 5,
    "Spinocerebellar_ataxia|_autosomal_recessive_33": 2,
    "Hereditary_methemoglobinemia": 1,
    "METHEMOGLOBINEMIA|_TYPE_II": 7,
    "not_provided|Neurodevelopmental_delay|CYB5R3-related_disorder": 1,
    "not_provided|Deficiency_of_cytochrome-b5_reductase|METHEMOGLOBINEMIA|_TYPE_I": 1,
    "Deficiency_of_cytochrome-b5_reductase|not_provided": 9,
    "CYB5R3-related_disorder|not_provided": 5,
    "Deficiency_of_cytochrome-b5_reductase": 25,
    "not_provided|Deficiency_of_cytochrome-b5_reductase": 6,
    "Deficiency_of_cytochrome-b5_reductase|METHEMOGLOBINEMIA|_TYPE_I": 1,
    "Hereditary_methemoglobinemia|Deficiency_of_cytochrome-b5_reductase|not_provided|Central_core_myopathy": 1,
    "METHEMOGLOBINEMIA|_TYPE_I|not_provided|Deficiency_of_cytochrome-b5_reductase": 1,
    "METHEMOGLOBINEMIA|_TYPE_I|Hereditary_methemoglobinemia": 1,
    "Inborn_genetic_diseases|Deficiency_of_cytochrome-b5_reductase|not_provided|not_specified": 1,
    "Deficiency_of_cytochrome-b5_reductase|CYB5R3-related_disorder|not_provided": 1,
    "not_provided|CYB5R3-related_disorder": 1,
    "METHEMOGLOBINEMIA|_TYPE_II|not_provided|Deficiency_of_cytochrome-b5_reductase": 1,
    "not_provided|Deficiency_of_cytochrome-b5_reductase|METHEMOGLOBINEMIA|_TYPE_II": 1,
    "METHEMOGLOBINEMIA|_TYPE_I": 4,
    "not_provided|CYB5R3-related_disorder|Deficiency_of_cytochrome-b5_reductase": 1,
    "not_provided|METHEMOGLOBINEMIA|_TYPE_I": 2,
    "CYB5R3_POLYMORPHISM|not_specified|not_provided": 1,
    "CYB5R3-related_disorder": 1,
    "Deficiency_of_cytochrome-b5_reductase|Inborn_genetic_diseases": 1,
    "METHEMOGLOBINEMIA|_TYPE_II|not_provided": 1,
    "Inborn_genetic_diseases|METHEMOGLOBINEMIA|_TYPE_I": 1,
    "Inborn_genetic_diseases|Deficiency_of_cytochrome-b5_reductase": 1,
    "Central_core_myopathy|Deficiency_of_cytochrome-b5_reductase": 1,
    "METHEMOGLOBINEMIA|_TYPE_I|not_provided|CYB5R3-related_disorder": 1,
    "not_provided|Deficiency_of_cytochrome-b5_reductase|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Deficiency_of_cytochrome-b5_reductase|not_provided": 1,
    "A4GALT-related_disorder|not_provided": 3,
    "not_provided|A4GALT-related_disorder": 3,
    "not_provided|p_phenotype": 1,
    "NOR_polyagglutination_syndrome": 1,
    "Blood_group|_P1PK_system": 4,
    "A4GALT-related_disorder": 1,
    "Infantile_cortical_hyperostosis|not_provided": 1,
    "Optic_atrophy_15": 2,
    "not_provided|MCAT-related_condition|Retinal_dystrophy": 1,
    "MCAT-related_condition": 1,
    "PNPLA5-related_disorder": 15,
    "NAFLD1": 43,
    "not_provided|NAFLD1": 5,
    "NAFLD1|not_provided": 20,
    "not_specified|NAFLD1": 3,
    "NAFLD1|not_specified": 6,
    "NAFLD1|not_provided|Hepatic_steatosis": 1,
    "not_specified|NAFLD1|not_provided": 1,
    "Susceptibility_to_Nonalcoholic_Fatty_Liver_Disease": 3,
    "Susceptibility_to_Nonalcoholic_Fatty_Liver_Disease|not_provided": 1,
    "Neurodevelopmental_disorder|not_specified|not_provided": 1,
    "not_provided|Renal_hypodysplasia/aplasia_1": 3,
    "UPK3A-related_disorder": 4,
    "Renal_hypodysplasia/aplasia_1|UPK3A-related_disorder|not_specified": 1,
    "not_provided|Renal_hypodysplasia/aplasia_1|UPK3A-related_disorder": 1,
    "UPK3A-related_disorder|not_specified": 2,
    "Renal_hypodysplasia/aplasia_1|UPK3A-related_disorder": 2,
    "not_specified|Renal_hypodysplasia/aplasia_1": 1,
    "Renal_hypodysplasia/aplasia_1|not_specified": 1,
    "UPK3A-related_disorder|Renal_hypodysplasia/aplasia_1|not_specified": 1,
    "not_specified|Renal_hypodysplasia/aplasia_1|UPK3A-related_disorder": 1,
    "UPK3A-related_disorder|not_provided": 1,
    "UPK3A-related_disorder|Congenital_anomalies_of_kidney_and_urinary_tract_1|Renal_hypodysplasia/aplasia_1|not_provided": 1,
    "UPK3A-related_disorder|Renal_hypodysplasia/aplasia_1": 1,
    "not_specified|Synpolydactyly_type_2": 1,
    "FBLN1-related_disorder": 10,
    "FBLN1-related_disorder|not_provided": 8,
    "Synpolydactyly_type_2|not_provided": 2,
    "Synpolydactyly_type_2": 2,
    "not_provided|FBLN1-related_disorder": 4,
    "not_specified|FBLN1-related_disorder|not_provided": 1,
    "Autosomal_recessive_syndrome_of_syndactyly|_undescended_testes_and_central_nervous_system_defects|not_provided": 1,
    "FBLN1-related_disorder|not_specified|not_provided": 3,
    "not_provided|FBLN1-related_disorder|not_specified": 1,
    "not_specified|not_provided|FBLN1-related_disorder": 1,
    "FBLN1-related_disorder|not_specified": 2,
    "not_provided|Synpolydactyly_type_2": 2,
    "Synpolydactyly_type_2|not_specified": 1,
    "Spinocerebellar_ataxia_type_10": 8,
    "ATXN10-related_disorder": 2,
    "not_specified|not_provided|Spinocerebellar_ataxia_type_10": 1,
    "ATXN10-related_disorder|Inborn_genetic_diseases": 1,
    "Matthew-Wood_syndrome|See_cases": 1,
    "PPARA-related_disorder": 2,
    "Hyperapobetalipoproteinemia|_susceptibility_to": 1,
    "not_provided|PPARA-related_disorder": 1,
    "Aminoglycoside-induced_deafness|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided": 5,
    "TRMU-related_disorder": 12,
    "not_specified|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 3,
    "TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "not_specified|TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "Aminoglycoside-induced_deafness": 32,
    "not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness": 6,
    "Aminoglycoside-induced_deafness|not_provided": 7,
    "not_provided|TRMU-related_disorder": 9,
    "not_provided|not_specified|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 4,
    "not_specified|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 3,
    "not_provided|Aminoglycoside-induced_deafness|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 6,
    "Deafness|_mitochondrial|_modifier_of|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness|not_provided|not_specified": 1,
    "TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness|not_provided": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_specified|not_provided": 1,
    "TRMU-related_disorder|not_provided": 5,
    "Aminoglycoside-induced_deafness|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 3,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness|not_provided": 8,
    "Inborn_genetic_diseases|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 2,
    "Aminoglycoside-induced_deafness|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 4,
    "TRMU-related_disorder|Aminoglycoside-induced_deafness|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided": 1,
    "TRMU-related_disorder|Inborn_genetic_diseases|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "not_provided|Aminoglycoside-induced_deafness": 9,
    "not_specified|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness|not_provided": 1,
    "not_provided|not_specified|TRMU-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided": 2,
    "not_provided|not_specified|TRMU-related_disorder": 1,
    "not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_specified": 3,
    "not_specified|not_provided|Aminoglycoside-induced_deafness": 1,
    "not_specified|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided": 3,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|TRMU-related_disorder": 2,
    "not_specified|not_provided|TRMU-related_disorder": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Inborn_genetic_diseases": 2,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness": 4,
    "not_provided|TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_specified": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_specified|not_provided|TRMU-related_disorder": 1,
    "TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_provided": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness|TRMU-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness": 1,
    "not_provided|TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Inborn_genetic_diseases": 1,
    "TRMU-related_disorder|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "not_provided|TRMU-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Inborn_genetic_diseases": 2,
    "not_provided|TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "Inborn_genetic_diseases|not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins": 1,
    "Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Aminoglycoside-induced_deafness|Inborn_genetic_diseases|not_provided": 1,
    "TRMU-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|TRMU-related_disorder|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|Inborn_genetic_diseases": 1,
    "not_provided|Acute_infantile_liver_failure_due_to_synthesis_defect_of_mtDNA-encoded_proteins|not_specified|TRMU-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|TRMU-related_disorder": 1,
    "CELSR1-related_disorder|not_provided": 15,
    "CELSR1-related_disorder": 77,
    "not_provided|CELSR1-related_disorder": 14,
    "not_specified|Lymphatic_malformation_9": 10,
    "not_specified|CELSR1-related_disorder": 4,
    "Yellow_nail_syndrome": 1,
    "Lymphatic_malformation_9": 27,
    "not_provided|Lymphatic_malformation_9|CELSR1-related_disorder": 1,
    "Mild_NDD": 2,
    "not_specified|Moderate_NDD": 1,
    "Lymphatic_malformation_9|Lymphatic_malformation": 2,
    "Lymphatic_malformation_9|not_specified": 2,
    "CELSR1-related_disorder|not_provided|not_specified": 1,
    "CELSR1-related_disorder|not_specified|not_provided|Lymphatic_malformation_9": 1,
    "Mild_to_moderate_NDD|not_provided": 1,
    "Severe_NDD|Walker-Warburg_congenital_muscular_dystrophy": 1,
    "CELSR1-related_disorder|not_specified": 1,
    "not_provided|Mild_to_moderate_NDD|not_specified": 1,
    "Moderate_NDD": 1,
    "Walker-Warburg_congenital_muscular_dystrophy|not_specified|Severe_NDD|_epilepsy": 1,
    "CELSR1-associated_congenital_heartdefects|not_specified": 1,
    "Lymphatic_malformation|Lymphatic_malformation_9": 1,
    "Rare": 1,
    "ALG12-congenital_disorder_of_glycosylation": 400,
    "ALG12-congenital_disorder_of_glycosylation|not_provided": 16,
    "ALG12-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 19,
    "ALG12-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|ALG12-congenital_disorder_of_glycosylation": 9,
    "Inborn_genetic_diseases|ALG12-congenital_disorder_of_glycosylation": 13,
    "not_provided|ALG12-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|ALG12-related_disorder": 1,
    "ALG12-congenital_disorder_of_glycosylation|ALG12-related_disorder": 7,
    "not_specified|not_provided|ALG12-congenital_disorder_of_glycosylation": 3,
    "ALG12-related_disorder|not_provided|ALG12-congenital_disorder_of_glycosylation": 2,
    "not_specified|ALG12-congenital_disorder_of_glycosylation": 2,
    "ALG12-congenital_disorder_of_glycosylation|ALG12-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|ALG12-congenital_disorder_of_glycosylation": 2,
    "ALG12-congenital_disorder_of_glycosylation|ALG12-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|ALG12-congenital_disorder_of_glycosylation|not_specified": 1,
    "ALG12-congenital_disorder_of_glycosylation|not_specified|not_provided": 4,
    "ALG12-related_disorder": 3,
    "not_specified|ALG12-congenital_disorder_of_glycosylation|not_provided": 1,
    "ALG12-congenital_disorder_of_glycosylation|not_specified": 4,
    "ALG12-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "ALG12-related_disorder|ALG12-congenital_disorder_of_glycosylation": 1,
    "ALG12-related_disorder|ALG12-congenital_disorder_of_glycosylation|not_provided": 1,
    "Inborn_genetic_diseases|ALG12-congenital_disorder_of_glycosylation|not_provided": 1,
    "ALG12-related_disorder|Inborn_genetic_diseases|ALG12-congenital_disorder_of_glycosylation": 1,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 47,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided": 22,
    "not_specified|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 4,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided|Inborn_genetic_diseases": 2,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 2,
    "not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Inborn_genetic_diseases|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 5,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "not_provided|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 3,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_specified": 2,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided": 6,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 5,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided": 4,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided|not_specified": 3,
    "not_provided|MLC1-related_disorder": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "not_specified|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 2,
    "not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided": 2,
    "not_provided|MLC1-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_specified": 1,
    "not_specified|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "not_provided|MLC1-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "MLC1-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_specified|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "MLC1-related_disorder|not_provided|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "MLC1-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_provided": 1,
    "MLC1-related_disorder|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 2,
    "not_provided|MLC1-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "MLC1-related_disorder|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1|not_provided": 1,
    "MLC1-related_disorder": 1,
    "not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_specified|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "MLC1-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "Megalencephalic_leukoencephalopathy_with_subcortical_cysts|MLC1-related_disorder|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "Inborn_genetic_diseases|Megalencephalic_leukoencephalopathy_with_subcortical_cysts": 1,
    "Macrocephaly|CNS_demyelination|Cerebellar_ataxia|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "not_provided|Abnormality_of_the_nervous_system|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|Megalencephalic_leukoencephalopathy_with_subcortical_cysts_1": 1,
    "MLC1-related_disorder|not_provided|Megalencephalic_leukoencephalopathy_with_subcortical_cysts|not_specified": 1,
    "Spermatogenic_failure_73|Non-obstructive_azoospermia": 2,
    "Non-obstructive_azoospermia|Spermatogenic_failure_73": 1,
    "Spermatogenic_failure_73": 1,
    "Microcephaly_and_chorioretinopathy_1": 29,
    "not_provided|Microcephaly_and_chorioretinopathy_1": 18,
    "TUBGCP6-related_disorder|not_provided": 26,
    "Microcephaly_and_chorioretinopathy_1|not_provided": 18,
    "not_provided|Microcephaly_and_chorioretinopathy_1|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Microcephaly_and_chorioretinopathy_1": 4,
    "Microcephaly_and_chorioretinopathy_1|not_provided|not_specified": 3,
    "not_provided|TUBGCP6-related_disorder": 16,
    "TUBGCP6-related_disorder": 5,
    "Inborn_genetic_diseases|Microcephaly_and_chorioretinopathy_1|not_provided": 2,
    "TUBGCP6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "TUBGCP6-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|TUBGCP6-related_disorder|not_specified": 2,
    "not_provided|Microcephaly_and_chorioretinopathy_1|not_specified": 2,
    "not_specified|TUBGCP6-related_disorder|not_provided": 1,
    "Microcephaly_and_chorioretinopathy_1|not_provided|Inborn_genetic_diseases": 4,
    "Microcephaly_and_chorioretinopathy_1|not_specified|not_provided": 2,
    "Microcephaly_and_chorioretinopathy_1|Inborn_genetic_diseases|not_provided": 3,
    "Retinal_dystrophy|not_provided|Microcephaly_and_chorioretinopathy_1": 1,
    "Inborn_genetic_diseases|Retinal_dystrophy|not_provided|Microcephaly_and_chorioretinopathy_1": 1,
    "TUBGCP6-related_disorder|not_specified|not_provided": 1,
    "Microcephaly_and_chorioretinopathy_with_or_without_intellectual_disability": 1,
    "not_specified|Microcephaly_and_chorioretinopathy_1": 1,
    "Inborn_genetic_diseases|not_provided|Microcephaly_and_chorioretinopathy_1": 1,
    "not_provided|TUBGCP6-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|not_provided|TUBGCP6-related_disorder": 1,
    "Inborn_genetic_diseases|TUBGCP6-related_disorder|not_provided": 1,
    "Microcephaly_and_chorioretinopathy_1|Microcephaly_and_chorioretinopathy_with_or_without_intellectual_disability|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|TUBGCP6-related_disorder|not_provided": 1,
    "Microcephaly_and_chorioretinopathy_1|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|TUBGCP6-related_disorder": 1,
    "Charcot-Marie-Tooth_disease_type_4B3": 14,
    "SBF1-related_disorder|not_provided": 20,
    "Charcot-Marie-Tooth_disease_type_4B3|not_provided": 40,
    "not_specified|Charcot-Marie-Tooth_disease_type_4B3|not_provided": 6,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B3": 5,
    "Charcot-Marie-Tooth_disease_type_4B3|not_provided|not_specified": 5,
    "not_specified|SBF1-related_disorder|Charcot-Marie-Tooth_disease_type_4B3|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B3|not_specified|not_provided": 9,
    "Peripheral_neuropathy|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_type_4B3": 2,
    "not_provided|SBF1-related_disorder": 10,
    "Charcot-Marie-Tooth_disease_type_4B3|not_provided|SBF1-related_disorder": 6,
    "not_specified|Charcot-Marie-Tooth_disease_type_4B3": 1,
    "SBF1-related_disorder": 7,
    "Charcot-Marie-Tooth_disease_type_4B3|not_specified|not_provided|Tip-toe_gait": 1,
    "SBF1-related_disorder|Tip-toe_gait|Charcot-Marie-Tooth_disease_type_4B3|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B3": 24,
    "not_provided|not_specified|Tip-toe_gait|Charcot-Marie-Tooth_disease_type_4B3": 1,
    "not_specified|SBF1-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_4B3|Charcot-Marie-Tooth_disease_X-linked_dominant_1|SBF1-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_type_4B3": 2,
    "not_provided|Charcot-Marie-Tooth_disease_type_4B3|not_specified": 5,
    "SBF1-related_disorder|Charcot-Marie-Tooth_disease_type_4B3|not_provided": 5,
    "SBF1-related_disorder|not_specified|not_provided|Charcot-Marie-Tooth_disease_type_4B3|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_disease_type_4B3|not_specified": 1,
    "SBF1-related_disorder|not_provided|not_specified": 1,
    "not_provided|SBF1-related_disorder|Charcot-Marie-Tooth_disease_type_4B3": 1,
    "Charcot-Marie-Tooth_disease_type_4B3|not_provided|Microcephaly": 1,
    "SBF1-related_disorder|Charcot-Marie-Tooth_disease_type_4B3|not_specified|not_provided": 1,
    "SBF1-related_disorder|not_specified|Charcot-Marie-Tooth_disease_type_4B3|not_provided": 1,
    "Myopia_6|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided": 2,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Myopia_6|not_provided": 5,
    "SCO2-related_disorder|not_provided": 2,
    "Fatal_Infantile_Cardioencephalomyopathy|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 15,
    "Myopia_6|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 4,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided": 8,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Myopia_6": 6,
    "Fatal_Infantile_Cardioencephalomyopathy|not_specified|not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Myopia_6|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 4,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|SCO2-related_disorder|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided": 1,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "not_provided|Inborn_genetic_diseases|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Myopia_6": 1,
    "not_provided|Myopia_6": 1,
    "Fatal_Infantile_Cardioencephalomyopathy|not_specified|not_provided|Myopia_6|Mitochondrial_DNA_depletion_syndrome_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "SCO2-related_disorder": 2,
    "Mitochondrial_DNA_depletion_syndrome_1|not_specified|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Fatal_Infantile_Cardioencephalomyopathy|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|SCO2-related_disorder|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Inborn_genetic_diseases|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 7,
    "SCO2-related_disorder|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Myopia_6|not_provided|Tip-toe_gait|Severe_global_developmental_delay|Seizure": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Myopia_6|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|not_specified|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|SCO2-related_disorder": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_specified|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 3,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Myopia_6|Inborn_genetic_diseases|not_provided": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|SCO2-related_disorder": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 1,
    "Inborn_genetic_diseases|not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|not_specified": 1,
    "not_specified|not_provided|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Inborn_genetic_diseases": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Myopia_6": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Myopia_6|Primary_dilated_cardiomyopathy": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 3,
    "Alagille_syndrome_due_to_a_JAG1_point_mutation|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1": 1,
    "Fatal_Infantile_Cardioencephalomyopathy|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|Myopia_6|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided": 1,
    "Fatal_Infantile_Cardioencephalomyopathy|not_specified|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 2,
    "TYMP-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_1": 96,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_1": 28,
    "TYMP-related_disorder|Mitochondrial_neurogastrointestinal_encephalomyopathy|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|not_specified": 1,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1|TYMP-related_disorder": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|not_provided": 20,
    "not_provided|TYMP-related_disorder": 4,
    "Mitochondrial_DNA_depletion_syndrome_1|not_provided": 20,
    "Fatal_Infantile_Cardioencephalomyopathy|Spinal_muscular_atrophy|not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "not_provided|Mitochondrial_neurogastrointestinal_encephalomyopathy": 14,
    "TYMP-related_disorder|Mitochondrial_neurogastrointestinal_encephalomyopathy|Fatal_Infantile_Cardioencephalomyopathy|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Inborn_genetic_diseases|Mitochondrial_neurogastrointestinal_encephalomyopathy": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|Inborn_genetic_diseases|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "not_provided|Mitochondrial_neurogastrointestinal_encephalomyopathy|Inborn_genetic_diseases": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|not_specified|not_provided": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1|Cardioencephalomyopathy|_fatal_infantile|_due_to_cytochrome_c_oxidase_deficiency_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "TYMP-related_disorder|Mitochondrial_neurogastrointestinal_encephalomyopathy|not_provided": 2,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided": 1,
    "not_specified|Mitochondrial_DNA_depletion_syndrome_1": 2,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 5,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_1|Inborn_genetic_diseases": 3,
    "TYMP-related_disorder|not_provided": 6,
    "Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Fatal_Infantile_Cardioencephalomyopathy": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided": 1,
    "Inborn_genetic_diseases|Mitochondrial_DNA_depletion_syndrome_1": 2,
    "Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "TYMP-related_disorder|Mitochondrial_DNA_depletion_syndrome_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "TYMP-related_disorder|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Fatal_Infantile_Cardioencephalomyopathy|not_provided": 1,
    "Fatal_Infantile_Cardioencephalomyopathy|Spinal_muscular_atrophy|not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Fatal_Infantile_Cardioencephalomyopathy|Mitochondrial_neurogastrointestinal_encephalomyopathy|not_specified|Mitochondrial_DNA_depletion_syndrome_1|not_provided|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|not_specified|not_provided": 4,
    "not_provided|Mitochondrial_neurogastrointestinal_encephalomyopathy|Mitochondrial_DNA_depletion_syndrome_1|TYMP-related_disorder": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|not_provided|not_specified|Fatal_Infantile_Cardioencephalomyopathy|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_neurogastrointestinal_encephalomyopathy": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|not_specified": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|not_provided|Mitochondrial_neurogastrointestinal_encephalomyopathy": 2,
    "Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_neurogastrointestinal_encephalomyopathy|not_provided": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|not_provided|not_specified": 1,
    "Mitochondrial_neurogastrointestinal_encephalomyopathy|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Mitochondrial_DNA_depletion_syndrome_1": 2,
    "not_provided|TYMP-related_disorder|Mitochondrial_neurogastrointestinal_encephalomyopathy": 1,
    "not_provided|Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_neurogastrointestinal_encephalomyopathy": 2,
    "Inborn_genetic_diseases|Intestinal_pseudo-obstruction": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_neurogastrointestinal_encephalomyopathy": 1,
    "TYMP-related_disorder|not_specified|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Mitochondrial_neurogastrointestinal_encephalomyopathy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Mitochondrial_DNA_depletion_syndrome_1|Inborn_genetic_diseases|not_provided": 1,
    "CPT1B-related_disorder": 4,
    "not_provided|Megaconial_type_congenital_muscular_dystrophy": 13,
    "Megaconial_type_congenital_muscular_dystrophy": 286,
    "Inborn_genetic_diseases|Megaconial_type_congenital_muscular_dystrophy": 14,
    "Megaconial_type_congenital_muscular_dystrophy|not_provided": 6,
    "Megaconial_type_congenital_muscular_dystrophy|Inborn_genetic_diseases": 9,
    "not_specified|not_provided|Megaconial_type_congenital_muscular_dystrophy": 4,
    "Inborn_genetic_diseases|not_provided|Megaconial_type_congenital_muscular_dystrophy": 1,
    "Megaconial_type_congenital_muscular_dystrophy|Inborn_genetic_diseases|not_provided": 3,
    "CHKB-related_disorder|Megaconial_type_congenital_muscular_dystrophy": 1,
    "Megaconial_type_congenital_muscular_dystrophy|not_specified": 5,
    "Megaconial_type_congenital_muscular_dystrophy|Congenital_Muscular_Dystrophy|_CHKB-related": 1,
    "Megaconial_type_congenital_muscular_dystrophy|CHKB-related_disorder": 1,
    "Megaconial_type_congenital_muscular_dystrophy|not_specified|CHKB-related_disorder|not_provided": 1,
    "not_provided|CHKB-related_disorder|Megaconial_type_congenital_muscular_dystrophy": 1,
    "Megaconial_type_congenital_muscular_dystrophy|Congenital_Muscular_Dystrophy|_CHKB-related|not_specified": 1,
    "Megaconial_type_congenital_muscular_dystrophy|CHKB-related_disorder|not_specified": 1,
    "CHKB-related_disorder|not_provided|Megaconial_type_congenital_muscular_dystrophy": 1,
    "not_specified|Megaconial_type_congenital_muscular_dystrophy": 4,
    "CHKB-related_disorder": 1,
    "not_provided|not_specified|Megaconial_type_congenital_muscular_dystrophy": 1,
    "not_provided|Megaconial_type_congenital_muscular_dystrophy|Inborn_genetic_diseases": 1,
    "Megaconial_type_congenital_muscular_dystrophy|CHKB-related_disorder|not_provided": 1,
    "not_specified|Megaconial_type_congenital_muscular_dystrophy|not_provided": 1,
    "not_specified|CHKB-related_disorder|Megaconial_type_congenital_muscular_dystrophy|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Megaconial_type_congenital_muscular_dystrophy": 1,
    "not_provided|Megaconial_type_congenital_muscular_dystrophy|not_specified": 1,
    "Metachromatic_leukodystrophy|not_provided": 45,
    "See_cases|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|ARSA-related_disorder": 5,
    "ARSA-related_disorder": 2,
    "not_specified|Metachromatic_leukodystrophy|not_provided|ARYLSULFATASE_A_PSEUDODEFICIENCY": 1,
    "not_provided|Metachromatic_leukodystrophy": 62,
    "not_specified|not_provided|Metachromatic_leukodystrophy": 7,
    "Inborn_genetic_diseases|Metachromatic_leukodystrophy": 12,
    "Metachromatic_leukodystrophy|ARSA-related_disorder|not_provided": 1,
    "ARYLSULFATASE_A_PSEUDODEFICIENCY": 3,
    "not_provided|Metachromatic_leukodystrophy|ARSA-related_disorder": 3,
    "Metachromatic_leukodystrophy|_late_infantile_form|not_provided|Metachromatic_leukodystrophy": 2,
    "ARSA-related_disorder|Metachromatic_leukodystrophy": 6,
    "Metachromatic_leukodystrophy|_juvenile_type": 2,
    "Metachromatic_leukodystrophy|not_provided|Inborn_genetic_diseases": 1,
    "ARSA-related_disorder|not_provided|Metachromatic_leukodystrophy|_juvenile_type|Metachromatic_leukodystrophy|_adult_type|.|Metachromatic_leukodystrophy|See_cases|Intellectual_disability": 1,
    "not_specified|Metachromatic_leukodystrophy": 8,
    "Metachromatic_leukodystrophy|METACHROMATIC_LEUKODYSTROPHY|_MILD": 1,
    "Metachromatic_leukodystrophy|_adult_type|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|not_provided|ARSA-related_disorder": 2,
    "not_provided|Metachromatic_leukodystrophy|not_specified": 3,
    "not_provided|Metachromatic_leukodystrophy|Metachromatic_leukodystrophy|_juvenile_type": 1,
    "Metachromatic_leukodystrophy|not_provided|Inborn_genetic_diseases|Neurodevelopmental_disorder": 1,
    "not_provided|Metachromatic_leukodystrophy|ARYLSULFATASE_A_PSEUDODEFICIENCY|_INTERMEDIATE": 1,
    "not_specified|Metachromatic_leukodystrophy|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Metachromatic_leukodystrophy": 2,
    "not_provided|ARYLSULFATASE_A_PSEUDODEFICIENCY|_SEVERE|Metachromatic_leukodystrophy": 1,
    "Inborn_genetic_diseases|Metachromatic_leukodystrophy|not_provided": 1,
    "METACHROMATIC_LEUKODYSTROPHY|_MILD|Metachromatic_leukodystrophy": 1,
    "not_provided|Metachromatic_leukodystrophy|METACHROMATIC_LEUKODYSTROPHY|_SEVERE": 1,
    "not_specified|not_provided|Metachromatic_leukodystrophy|_juvenile_type|Metachromatic_leukodystrophy": 1,
    "Leukodystrophy|not_provided|Metachromatic_leukodystrophy|METACHROMATIC_LEUKODYSTROPHY|_SEVERE": 1,
    "Metachromatic_leukodystrophy|not_specified": 8,
    "not_provided|not_specified|Metachromatic_leukodystrophy": 4,
    "Metachromatic_leukodystrophy|Autosomal_recessive_sideroblastic_anemia": 1,
    "not_provided|PSEUDOARYLSULFATASE_A_DEFICIENCY|Metachromatic_leukodystrophy|Metachromatic_leukodystrophy|_late_infantile_form|Abnormality_of_the_nervous_system": 1,
    "not_provided|Metachromatic_leukodystrophy|_late_infantile_form": 1,
    "Metachromatic_leukodystrophy|METACHROMATIC_LEUKODYSTROPHY|_SEVERE": 2,
    "Neurologic|_endocrine|_and_pancreatic_disease|_multisystem|_infantile-onset_2|not_provided|Metachromatic_leukodystrophy": 1,
    "ARSA-related_disorder|Inborn_genetic_diseases|not_provided|Metachromatic_leukodystrophy": 2,
    "Spastic_ataxia|not_provided|Metachromatic_leukodystrophy": 1,
    "ARSA-related_disorder|Metachromatic_leukodystrophy|_adult_type|Metachromatic_leukodystrophy": 1,
    "not_provided|METACHROMATIC_LEUKODYSTROPHY|_SEVERE|Metachromatic_leukodystrophy": 1,
    "ARSA-related_disorder|Metachromatic_leukodystrophy|METACHROMATIC_LEUKODYSTROPHY|_SEVERE|not_provided": 1,
    "not_provided|Metachromatic_leukodystrophy|Metachromatic_leukodystrophy|_late_infantile_form": 1,
    "METACHROMATIC_LEUKODYSTROPHY|_SEVERE|not_provided|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|_juvenile_type|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|Inborn_genetic_diseases|not_provided": 1,
    "Citrullinemia|not_specified|not_provided|Metachromatic_leukodystrophy": 1,
    "not_specified|Inborn_genetic_diseases|Metachromatic_leukodystrophy": 1,
    "Inborn_genetic_diseases|not_provided|Metachromatic_leukodystrophy|_juvenile_type|Metachromatic_leukodystrophy|Metachromatic_leukodystrophy|_adult_type": 1,
    "not_specified|not_provided|Metachromatic_leukodystrophy|ARYLSULFATASE_A_PSEUDODEFICIENCY|Intellectual_disability": 1,
    "not_provided|ARSA-related_disorder|Metachromatic_leukodystrophy": 1,
    "ARSA-related_disorder|Inborn_genetic_diseases|Neurodevelopmental_disorder|not_provided|Metachromatic_leukodystrophy|Metachromatic_leukodystrophy|_adult_type|Metachromatic_leukodystrophy|_juvenile_type|See_cases|Intellectual_disability": 1,
    "Metachromatic_leukodystrophy|not_provided|not_specified": 1,
    "Metachromatic_leukodystrophy|not_specified|not_provided|Citrullinemia": 1,
    "not_provided|Metachromatic_leukodystrophy|Inborn_genetic_diseases": 1,
    "METACHROMATIC_LEUKODYSTROPHY|_SEVERE|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|_adult_type": 1,
    "Inborn_genetic_diseases|not_provided|Metachromatic_leukodystrophy": 1,
    "not_provided|Metachromatic_leukodystrophy|_adult_type|Metachromatic_leukodystrophy": 1,
    "not_provided|Metachromatic_leukodystrophy|_late_infantile_form|Metachromatic_leukodystrophy": 1,
    "not_provided|METACHROMATIC_LEUKODYSTROPHY|_SEVERE": 1,
    "not_provided|METACHROMATIC_LEUKODYSTROPHY|_LATE-ONSET|Metachromatic_leukodystrophy": 1,
    "Frontotemporal_dementia|not_provided|Metachromatic_leukodystrophy": 1,
    "Metachromatic_leukodystrophy|not_specified|not_provided": 2,
    "Phelan-McDermid_syndrome": 106,
    "SHANK3-related_disorder": 39,
    "Inborn_genetic_diseases|SHANK3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Seizure|Global_developmental_delay": 1,
    "Phelan-McDermid_syndrome|not_provided": 9,
    "SHANK3-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "SHANK3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|SHANK3-related_disorder": 2,
    "Phelan-McDermid_syndrome|Schizophrenia_15": 6,
    "Phelan-McDermid_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|SHANK3-related_disorder": 3,
    "Schizophrenia_15|Phelan-McDermid_syndrome|not_provided": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided": 1,
    "SHANK3-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "SHANK3-related_disorder|Inborn_genetic_diseases|not_specified": 2,
    "SHANK3-related_disorder|not_specified": 1,
    "not_provided|SHANK3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Phelan-McDermid_syndrome": 1,
    "Intellectual_disability|Abnormal_cerebral_white_matter_morphology|Hyperammonemia|Neurodegeneration": 1,
    "Schizophrenia_15": 1,
    "Atypical_behavior|not_provided": 1,
    "Inborn_genetic_diseases|SHANK3-related_disorder|not_specified": 1,
    "Phelan-McDermid_syndrome|Intellectual_disability|Neurodevelopmental_abnormality|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|SHANK3-related_disorder|Inborn_genetic_diseases|Schizophrenia_15|Phelan-McDermid_syndrome": 1,
    "not_provided|Phelan-McDermid_syndrome": 2,
    "not_provided|SHANK3-related_disorder|Inborn_genetic_diseases": 2,
    "SHANK3-related_disorder|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Hand_tremor|Macrocephaly|Atypical_behavior|Seizure": 1,
    "Schizophrenia_15|Phelan-McDermid_syndrome": 2,
    "Intellectual_disability|Schizophrenia_15": 1,
    "not_provided|Autism_spectrum_disorder|SHANK3-related_disorder|Phelan-McDermid_syndrome": 1,
    "not_provided|Schizophrenia_15|Phelan-McDermid_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|SHANK3-related_disorder": 1,
    "Moderate_global_developmental_delay|Psychotic_disorder|Mutism|Phelan-McDermid_syndrome|Schizophrenia_15": 1,
    "SHANK3-related_disorder|Neurodevelopmental_disorder|Inborn_genetic_diseases|Schizophrenia_15|Phelan-McDermid_syndrome|not_provided|Autism_spectrum_disorder": 1,
    "Neurodevelopmental_delay|not_provided|Intellectual_disability|Phelan-McDermid_syndrome|Schizophrenia_15": 1,
    "SHANK3-related_disorder|Inborn_genetic_diseases|not_provided|Phelan-McDermid_syndrome|Intellectual_disability|See_cases": 1,
    "Autism|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Schizophrenia_15|Phelan-McDermid_syndrome": 1,
    "SHANK3-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|SHANK3-related_disorder": 1,
    "not_provided|Intellectual_disability|Phelan-McDermid_syndrome": 1,
    "Phelan-McDermid_syndrome|Intellectual_disability": 1,
    "SHANK3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Phelan-McDermid_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "not_provided|Phelan-McDermid_syndrome|Autistic_behavior": 1,
    "Spermatogenic_failure_87": 1,
    "SHOX-related_disorder": 8,
    "SHOX-related_short_stature": 13,
    "SHOX-related_disorder|not_specified|Langer_mesomelic_dysplasia_syndrome|SHOX-related_short_stature|Leri-Weill_dyschondrosteosis|not_provided": 1,
    "Connective_tissue_disorder|not_specified|SHOX-related_short_stature|Leri-Weill_dyschondrosteosis": 1,
    "not_specified|Leri-Weill_dyschondrosteosis|not_provided": 1,
    "not_specified|SHOX-related_short_stature": 1,
    "not_specified|not_provided|Leri-Weill_dyschondrosteosis|SHOX-related_disorder|Connective_tissue_disorder": 1,
    "SHOX-related_short_stature|Leri-Weill_dyschondrosteosis": 1,
    "Langer_mesomelic_dysplasia_syndrome": 3,
    "Leri-Weill_dyschondrosteosis": 18,
    "SHOX-related_short_stature|Connective_tissue_disorder|Langer_mesomelic_dysplasia_syndrome|Leri-Weill_dyschondrosteosis|not_provided|not_specified": 1,
    "Leri-Weill_dyschondrosteosis|SHOX-related_short_stature|Langer_mesomelic_dysplasia_syndrome": 3,
    "not_specified|not_provided|SHOX-related_short_stature": 1,
    "not_specified|not_provided|Leri-Weill_dyschondrosteosis": 1,
    "not_provided|Langer_mesomelic_dysplasia_syndrome": 1,
    "not_provided|SHOX-related_short_stature": 3,
    "not_provided|Leri-Weill_dyschondrosteosis": 2,
    "Leri-Weill_dyschondrosteosis|Langer_mesomelic_dysplasia_syndrome|SHOX-related_short_stature": 1,
    "SHOX-related_short_stature|Connective_tissue_disorder|not_provided": 1,
    "Langer_mesomelic_dysplasia_syndrome|Leri-Weill_dyschondrosteosis": 2,
    "Leri-Weill_dyschondrosteosis|not_provided": 1,
    "Langer_mesomelic_dysplasia_syndrome|Leri-Weill_dyschondrosteosis|not_provided": 1,
    "Short_stature|SHOX-related_disorder": 1,
    "not_specified|Leri-Weill_dyschondrosteosis": 1,
    "Leri-Weill_dyschondrosteosis|Langer_mesomelic_dysplasia_syndrome": 1,
    "SHOX-related_disorder|Leri-Weill_dyschondrosteosis|not_provided": 1,
    "not_specified|SHOX-related_disorder": 2,
    "Langer_mesomelic_dysplasia_syndrome|Leri-Weill_dyschondrosteosis|SHOX-related_short_stature|not_specified|not_provided": 1,
    "SHOX-related_disorder|SHOX-related_short_stature|Leri-Weill_dyschondrosteosis|not_provided": 1,
    "not_specified|SHOX-related_short_stature|Leri-Weill_dyschondrosteosis|Langer_mesomelic_dysplasia_syndrome": 1,
    "Leri-Weill_dyschondrosteosis|Langer_mesomelic_dysplasia_syndrome|not_provided": 1,
    "not_specified|not_provided|SHOX-related_disorder": 1,
    "SHOX-related_disorder|not_provided": 1,
    "not_specified|SHOX-related_short_stature|not_provided": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_4": 310,
    "not_specified|CSF2RA-related_disorder|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_4": 1,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_4": 7,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_4|CSF2RA-related_disorder": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_4|not_provided": 9,
    "not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_4|not_specified": 3,
    "not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_4": 3,
    "Surfactant_metabolism_dysfunction|_pulmonary|_4|CSF2RA-related_disorder": 3,
    "not_specified|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_4": 1,
    "CSF2RA-related_disorder|Surfactant_metabolism_dysfunction|_pulmonary|_4": 3,
    "Surfactant_metabolism_dysfunction|_pulmonary|_4|not_provided|not_specified": 1,
    "CSF2RA-related_disorder|not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_4|not_provided": 1,
    "CSF2RA-related_disorder|Surfactant_metabolism_dysfunction|_pulmonary|_4|not_specified": 1,
    "not_specified|CSF2RA-related_disorder|Surfactant_metabolism_dysfunction|_pulmonary|_4": 1,
    "Decreased_B_cell_survival_and_tolerance": 1,
    "CSF2RA-related_disorder|not_provided|Surfactant_metabolism_dysfunction|_pulmonary|_4": 1,
    "not_provided|not_specified|Surfactant_metabolism_dysfunction|_pulmonary|_4": 1,
    "Surfactant_metabolism_dysfunction|_pulmonary|_4|CSF2RA-related_disorder|not_provided": 1,
    "CSF2RA-related_disorder": 3,
    "not_specified|not_provided|CSF2RA-related_disorder|Surfactant_metabolism_dysfunction|_pulmonary|_4": 1,
    "CSF2RA-related_disorder|not_specified": 1,
    "not_provided|CSF2RA-related_disorder|not_specified": 1,
    "SLC25A6-related_disorder": 3,
    "ASMT-related_disorder|not_provided": 1,
    "ASMT-related_disorder": 5,
    "Congenital_disorder_of_glycosylation|_type_1DD": 1,
    "CD99_Positive_Neoplastic_Cells_Present": 1,
    "XG_BLOOD_GROUP_SYSTEM|_Xg(a-)_PHENOTYPE": 1,
    "not_provided|GYG2-related_disorder": 2,
    "GYG2-related_disorder|not_provided": 3,
    "not_specified|not_provided|GYG2-related_disorder": 3,
    "Atypical_Leigh_syndrome": 1,
    "GYG2-related_disorder|not_provided|not_specified": 2,
    "not_specified|ARSD-related_disorder": 3,
    "ARSD-related_disorder": 17,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 229,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Inborn_genetic_diseases|not_provided|X-linked_chondrodysplasia_punctata_1|See_cases": 1,
    "X-linked_chondrodysplasia_punctata_1": 23,
    "not_specified|not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "not_provided|X-linked_chondrodysplasia_punctata_1|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_specified|not_provided|X-linked_chondrodysplasia_punctata_1": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_specified": 2,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided|not_specified": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Connective_tissue_disorder": 2,
    "Inborn_genetic_diseases|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 6,
    "not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 5,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Inborn_genetic_diseases": 5,
    "not_provided|X-linked_chondrodysplasia_punctata_1|ARSL-related_disorder|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "Inborn_genetic_diseases|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided": 2,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|ARSL-related_disorder|not_provided": 2,
    "ARSL-related_disorder|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 2,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|X-linked_chondrodysplasia_punctata_1|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|X-linked_chondrodysplasia_punctata_1": 1,
    "not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|ARSL-related_disorder|Inborn_genetic_diseases": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|X-linked_chondrodysplasia_punctata_1": 4,
    "Inborn_genetic_diseases|not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Connective_tissue_disorder|Inborn_genetic_diseases|X-linked_chondrodysplasia_punctata_1|not_specified": 1,
    "not_provided|X-linked_chondrodysplasia_punctata_1": 5,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided": 8,
    "not_provided|Inborn_genetic_diseases|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "X-linked_chondrodysplasia_punctata_1|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 2,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_specified|not_provided": 1,
    "X-linked_chondrodysplasia_punctata_1|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided": 1,
    "not_specified|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "not_provided|X-linked_chondrodysplasia_punctata_1|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Connective_tissue_disorder|not_specified": 1,
    "not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Connective_tissue_disorder|not_specified|X-linked_chondrodysplasia_punctata_1": 1,
    "Dystonia|_early-onset|_and/or_spastic_paraplegia|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "Inborn_genetic_diseases|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|X-linked_chondrodysplasia_punctata_1|Connective_tissue_disorder": 1,
    "not_specified|X-linked_chondrodysplasia_punctata_1|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided|Connective_tissue_disorder": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided|X-linked_chondrodysplasia_punctata_1|Inborn_genetic_diseases|Intellectual_disability": 1,
    "X-linked_chondrodysplasia_punctata_1|not_specified|not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Connective_tissue_disorder": 1,
    "ARSL-related_disorder|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_specified|not_provided|Coffin-Siris_syndrome_1|X-linked_chondrodysplasia_punctata_1": 1,
    "X-linked_chondrodysplasia_punctata_1|not_provided": 1,
    "Inborn_genetic_diseases|Connective_tissue_disorder|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "ARSL-related_disorder": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Connective_tissue_disorder|not_specified|not_provided|X-linked_chondrodysplasia_punctata_1": 1,
    "not_provided|ARSL-related_disorder": 1,
    "not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|Inborn_genetic_diseases": 1,
    "ARSL-related_disorder|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided|Connective_tissue_disorder": 1,
    "Chondrodysplasia_punctata|_brachytelephalangic|_autosomal|not_provided|X-linked_chondrodysplasia_punctata_1": 1,
    "X-linked_chondrodysplasia_punctata_1|ARSL-related_disorder|not_provided": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "X-linked_chondrodysplasia_punctata_1|not_provided|Chondrodysplasia_punctata|_brachytelephalangic|_autosomal": 1,
    "ARSL-related_disorder|Connective_tissue_disorder|Epilepsy": 1,
    "X-linked_chondrodysplasia_punctata_1|ARSL-related_disorder|not_provided|Connective_tissue_disorder": 1,
    "ARSH-related_condition": 1,
    "ARSF-related_disorder": 8,
    "not_provided|ARSF-related_disorder": 2,
    "MXRA5-related_disorder": 1,
    "Autism|_susceptibility_to|_X-linked_2": 16,
    "NLGN4X-related_disorder": 13,
    "Inborn_genetic_diseases|not_specified|not_provided|Autism|_susceptibility_to|_X-linked_2": 2,
    "NLGN4X-related_disorder|Inborn_genetic_diseases": 1,
    "Autism|_susceptibility_to|_X-linked_2|not_provided": 3,
    "NLGN4X-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Autism|_susceptibility_to|_X-linked_2|Asperger_syndrome|_X-linked|_susceptibility_to|_2|not_provided": 1,
    "NLGN4X-related_disorder|not_provided|not_specified": 1,
    "NLGN4X-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "NLGN4X-related_disorder|not_provided": 4,
    "not_provided|NLGN4X-related_disorder|Inborn_genetic_diseases": 1,
    "NLGN4X-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|NLGN4X-related_disorder": 3,
    "Inborn_genetic_diseases|not_provided|NLGN4X-related_disorder": 1,
    "Inborn_genetic_diseases|Autism|_susceptibility_to|_X-linked_2": 2,
    "Asperger_syndrome|_X-linked|_susceptibility_to|_2": 1,
    "Autism|_susceptibility_to|_X-linked_2|X-linked_intellectual_disability": 1,
    "Autism|_susceptibility_to|_X-linked_2|Inborn_genetic_diseases": 1,
    "NLGN4X-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Asperger_syndrome|_X-linked|_susceptibility_to|_2|Autism|_susceptibility_to|_X-linked_2": 1,
    "not_provided|Asperger_syndrome|_X-linked|_susceptibility_to|_2|Autism|_susceptibility_to|_X-linked_2": 1,
    "VCX3A-related_disorder": 8,
    "not_provided|STS-related_disorder": 5,
    "STS-related_disorder|not_provided": 2,
    "X-linked_ichthyosis_with_steryl-sulfatase_deficiency": 15,
    "X-linked_ichthyosis_with_steryl-sulfatase_deficiency|not_provided": 4,
    "not_provided|X-linked_ichthyosis_with_steryl-sulfatase_deficiency": 2,
    "X-linked_ichthyosis_with_steryl-sulfatase_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "STS-related_disorder": 1,
    "STS-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "PNPLA4-related_disorder|not_provided": 1,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 156,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_specified|Amenorrhea": 1,
    "not_provided|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|Martsolf_syndrome_1": 1,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 8,
    "not_specified|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_provided": 1,
    "not_provided|Amenorrhea|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_specified": 1,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|Inborn_genetic_diseases": 6,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_specified|not_provided": 3,
    "not_provided|not_specified|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 2,
    "not_provided|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 8,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_provided": 4,
    "not_specified|not_provided|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 3,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|Inborn_genetic_diseases|not_provided": 1,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|Hypogonadotropic_hypogonadism": 1,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|Hypogonadotropic_hypogonadism_7_with_or_without_anosmia|Delayed_puberty": 1,
    "ANOS1-related_disorder": 7,
    "Amenorrhea|ANOS1-related_disorder": 1,
    "Inborn_genetic_diseases|ANOS1-related_disorder": 1,
    "not_provided|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_specified": 1,
    "ANOS1-related_disorder|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 2,
    "ANOS1-related_disorder|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_provided": 1,
    "not_provided|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|Inborn_genetic_diseases": 1,
    "ANOS1-related_disorder|Micropenis": 1,
    "not_specified|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia": 2,
    "Inborn_genetic_diseases|Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|ANOS1-related_disorder": 1,
    "Hypogonadotropic_hypogonadism_1_with_or_without_anosmia|not_specified": 1,
    "TBL1X-related_disorder|not_provided": 1,
    "TBL1X-related_disorder": 3,
    "Hypothyroidism|_congenital|_nongoitrous|_8|not_provided": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_8": 8,
    "not_provided|Hypothyroidism|_congenital|_nongoitrous|_8": 2,
    "TBL1X-related_disorder|Hypothyroidism|_congenital|_nongoitrous|_8": 1,
    "GPR143-related_disorder|not_provided": 5,
    "not_provided|Ocular_albinism|_type_I|Nystagmus_6|_congenital|_X-linked": 1,
    "not_provided|GPR143-related_disorder|Inborn_genetic_diseases": 1,
    "Nystagmus_6|_congenital|_X-linked|not_provided": 3,
    "not_provided|GPR143-related_foveal_hypoplasia": 1,
    "Ocular_albinism|_type_I|Nystagmus_6|_congenital|_X-linked|not_provided": 2,
    "Ocular_albinism|_type_I": 9,
    "Ocular_albinism|_type_I|not_provided": 6,
    "not_provided|Albinism": 1,
    "not_provided|not_specified|Ocular_albinism|_type_I|Nystagmus_6|_congenital|_X-linked": 1,
    "Ocular_albinism|_type_I|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Ocular_albinism|_type_I": 6,
    "GPR143-related_disorder": 6,
    "not_provided|GPR143-related_disorder": 2,
    "not_specified|not_provided|Ocular_albinism|_type_I": 1,
    "Nystagmus_6|_congenital|_X-linked": 2,
    "not_provided|Nystagmus_6|_congenital|_X-linked": 1,
    "GPR143-related_disorder|Nystagmus_6|_congenital|_X-linked": 1,
    "Inborn_genetic_diseases|Ocular_albinism|_type_I|Nystagmus_6|_congenital|_X-linked|not_provided": 1,
    "Ocular_albinism|Reduced_eye_contact|Nystagmus|Ocular_albinism|_type_I|not_provided": 1,
    "Nystagmus_6|_congenital|_X-linked|Ocular_albinism|_type_I": 1,
    "SHROOM2-related_disorder": 40,
    "SHROOM2-related_disorder|not_specified": 3,
    "SHROOM2-related_disorder|not_provided": 4,
    "not_provided|SHROOM2-related_disorder": 1,
    "Intellectual_disability|_X-linked_49|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_49|not_provided": 1,
    "Intellectual_disability|_X-linked_49|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked_49": 58,
    "CLCN4-related_disorder|not_provided": 11,
    "CLCN4-related_disorder|not_provided|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_X-linked_81|Intellectual_disability|_X-linked_49": 1,
    "Intellectual_disability|_X-linked_49|not_provided": 8,
    "not_specified|CLCN4-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked_49": 13,
    "CLCN4-related_disorder": 8,
    "not_provided|not_specified|CLCN4-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Intellectual_disability|_X-linked_49|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_49": 1,
    "Intellectual_disability|_X-linked_49|CLCN4-related_disorder|not_provided": 1,
    "not_provided|CLCN4-related_disorder": 4,
    "not_provided|Intellectual_disability|_X-linked_49|CLCN4-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Intellectual_disability|_X-linked_49": 1,
    "Intellectual_disability|_X-linked_49|not_provided|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|not_provided|Intellectual_disability|_X-linked_49": 1,
    "Non-syndromic_X-linked_intellectual_disability|not_provided": 7,
    "not_provided|Intellectual_disability|_X-linked_49|CLCN4-related_disorder": 1,
    "Intellectual_disability|_X-linked_49|Inborn_genetic_diseases": 1,
    "not_provided|See_cases|Intellectual_disability|_X-linked_49|CLCN4-related_disorder": 1,
    "not_provided|Intellectual_disability|_X-linked_49|See_cases|Inborn_genetic_diseases": 1,
    "not_provided|CLCN4-related_disorder|Intellectual_disability|_X-linked_49": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|X-linked_Opitz_G/BBB_syndrome": 1,
    "MID1-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|MID1-related_disorder": 5,
    "X-linked_Opitz_G/BBB_syndrome": 41,
    "not_specified|not_provided|X-linked_Opitz_G/BBB_syndrome": 1,
    "not_provided|X-linked_Opitz_G/BBB_syndrome": 4,
    "Corpus_callosum|_agenesis_of|Low-set_ears|Abnormal_facial_shape|Clinodactyly_of_the_5th_finger|Hypertelorism": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|MID1-related_disorder": 1,
    "not_specified|X-linked_Opitz_G/BBB_syndrome|not_provided": 1,
    "X-linked_Opitz_G/BBB_syndrome|not_provided": 5,
    "MID1-related_disorder": 7,
    "MID1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|X-linked_Opitz_G/BBB_syndrome": 3,
    "Inborn_genetic_diseases|not_specified|MID1-related_disorder": 1,
    "Inborn_genetic_diseases|X-linked_Opitz_G/BBB_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|X-linked_Opitz_G/BBB_syndrome|not_specified": 1,
    "X-linked_Opitz_G/BBB_syndrome|Dandy-Walker_syndrome|not_provided": 1,
    "MID1-related_disorder|not_provided": 2,
    "not_specified|MID1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "X-linked_Opitz_G/BBB_syndrome|not_provided|not_specified|MID1-related_disorder|Inborn_genetic_diseases": 1,
    "X-linked_Opitz_G/BBB_syndrome|Inborn_genetic_diseases": 1,
    "Rhabdoid_tumor_predisposition_syndrome_2|Intellectual_disability|_autosomal_dominant_16|Otosclerosis_12": 1,
    "Linear_skin_defects_with_multiple_congenital_anomalies_1": 17,
    "not_provided|not_specified|Intellectual_disability|HCCS-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|HCCS-related_disorder": 2,
    "HCCS-related_disorder": 3,
    "not_provided|History_of_neurodevelopmental_disorder|not_specified": 2,
    "HCCS-related_disorder|not_provided": 1,
    "HCCS-related_disorder|not_provided|not_specified": 1,
    "HCCS-related_disorder|Linear_skin_defects_with_multiple_congenital_anomalies_1": 1,
    "not_provided|Linear_skin_defects_with_multiple_congenital_anomalies_1": 2,
    "not_provided|ARHGAP6-related_disorder": 1,
    "Amelogenesis_imperfecta_type_1E": 14,
    "Amelogenesis_imperfecta_type_1E|Inborn_genetic_diseases": 1,
    "Amelogenesis_imperfecta_type_1E|AMELX-related_disorder|not_provided": 1,
    "AMELX-related_disorder": 2,
    "not_provided|AMELX-related_disorder": 2,
    "AMELX-related_disorder|not_provided": 1,
    "MSL3-related_disorder": 10,
    "Basilicata-Akhtar_syndrome": 22,
    "MSL3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Basilicata-Akhtar_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|MSL3-related_disorder": 1,
    "Basilicata-Akhtar_syndrome|Intellectual_disability": 3,
    "Basilicata-Akhtar_syndrome|not_provided": 2,
    "Basilicata-Akhtar_syndrome|Intellectual_disability|not_provided": 2,
    "Inborn_genetic_diseases|Basilicata-Akhtar_syndrome": 1,
    "X-linked_neurodevelopmental_delay|_dysmorphism|_and_progressive_neurological_disorder": 1,
    "FRMPD4-related_disorder|not_specified": 2,
    "not_provided|Inborn_genetic_diseases|FRMPD4-related_disorder": 1,
    "FRMPD4-related_disorder": 13,
    "Intellectual_disability|_X-linked_104": 54,
    "FRMPD4-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Intellectual_disability|_X-linked_104|Inborn_genetic_diseases": 1,
    "FRMPD4-related_disorder|Intellectual_disability|_X-linked_104|not_provided": 1,
    "Autism|_susceptibility_to|_X-linked_4": 27,
    "FRMPD4-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Intellectual_disability|_X-linked_104|not_provided|not_specified": 1,
    "not_specified|not_provided|FRMPD4-related_disorder": 1,
    "not_specified|not_provided|Intellectual_disability|_X-linked_104": 1,
    "not_provided|FRMPD4-related_disorder": 2,
    "not_specified|Intellectual_disability|_X-linked_104|not_provided": 1,
    "FRMPD4-related_disorder|not_provided": 3,
    "Intellectual_disability|_X-linked_104|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_104": 1,
    "FRMPD4-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_104": 1,
    "FRMPD4-related_disorder|Intellectual_disability|_X-linked_104": 1,
    "FRMPD4-related_disorder|Intellectual_disability|_X-linked_104|not_provided|not_specified": 1,
    "X-linked_complex_neurodevelopmental_disorder": 3,
    "not_provided|Intellectual_disability|_X-linked_104": 2,
    "Intellectual_disability|_X-linked_104|not_provided": 1,
    "Autism|_susceptibility_to|_X-linked_4|not_specified|not_provided": 1,
    "Systemic_lupus_erythematosus_17": 1,
    "not_provided|not_specified|TLR7-related_disorder": 1,
    "TLR7-related_disorder|not_provided": 1,
    "Systemic_lupus_erythematosus_17|not_provided": 1,
    "not_provided|Systemic_lupus_erythematosus_17|Immunodeficiency_74|_COVID-19-related|_X-linked": 1,
    "not_provided|TLR7-related_disorder": 1,
    "Systemic_lupus_erythematosus_17|Systemic_lupus_erythematosus": 1,
    "TLR7-related_disorder": 1,
    "Immunodeficiency_74|_COVID-19-related|_X-linked": 2,
    "Systemic_lupus_erythematosus_17|not_specified|Systemic_lupus_erythematosus": 1,
    "Immunodeficiency_98_with_autoinflammation|_X-linked": 4,
    "Immunodeficiency_98_with_autoinflammation|_X-linked|not_specified": 1,
    "not_specified|TLR8-related_condition": 2,
    "INFLTR8|not_provided|TLR8-related_condition|Immunodeficiency_98_with_autoinflammation|_X-linked": 1,
    "INFLTR8|Immunodeficiency_98_with_autoinflammation|_X-linked": 1,
    "Immunodeficiency_98_with_autoinflammation|_X-linked|INFLTR8": 1,
    "Immunodeficiency_98_with_autoinflammation|_X-linked|Autoimmune_hemolytic_anemia|Systemic_autoinflammation": 1,
    "Autoimmune_hemolytic_anemia|Systemic_autoinflammation": 1,
    "not_specified|Exstrophy-epispadias_complex": 1,
    "Spondyloepiphyseal_dysplasia_tarda": 57,
    "Spondyloepiphyseal_dysplasia_tarda|not_provided": 7,
    "not_provided|Spondyloepiphyseal_dysplasia_tarda": 3,
    "Spondyloepiphyseal_dysplasia_tarda|_X-linked": 9,
    "not_provided|Spondyloepiphyseal_dysplasia_tarda|Hereditary_spastic_paraplegia_4": 1,
    "Connective_tissue_disorder|Spondyloepiphyseal_dysplasia_tarda": 1,
    "not_provided|Spondyloepiphyseal_dysplasia_tarda|_X-linked|TRAPPC2-related_disorder": 1,
    "not_provided|TRAPPC2-related_disorder": 1,
    "Spondyloepiphyseal_dysplasia_tarda|_X-linked|Inborn_genetic_diseases|not_provided|Spondyloepiphyseal_dysplasia_tarda": 1,
    "not_specified|not_provided|Spondyloepiphyseal_dysplasia_tarda": 1,
    "Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I": 36,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Primary_ciliary_dyskinesia|Joubert_syndrome_10": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I": 342,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia": 13,
    "Orofaciodigital_syndrome_I|Joubert_syndrome": 116,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2": 3,
    "not_provided|Joubert_syndrome|Orofaciodigital_syndrome_I": 8,
    "OFD1-related_disorder": 10,
    "not_provided|OFD1-related_ciliopathy": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "OFD1-related_disorder|Orofaciodigital_syndrome_I|Joubert_syndrome": 3,
    "Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome": 2,
    "not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome": 8,
    "Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Joubert_syndrome": 10,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|OFD1-related_disorder|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23": 1,
    "Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Joubert_syndrome": 3,
    "Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Joubert_syndrome": 2,
    "Joubert_syndrome_10|Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified": 3,
    "not_specified|Joubert_syndrome|Orofaciodigital_syndrome_I": 3,
    "not_provided|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided": 16,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Primary_ciliary_dyskinesia": 8,
    "OFD1-related_disorder|Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided|Primary_ciliary_dyskinesia": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 2,
    "Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Orofaciodigital_syndrome_I": 2,
    "not_provided|Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia": 3,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|not_specified": 1,
    "Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Joubert_syndrome": 15,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|Primary_ciliary_dyskinesia": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Retinal_dystrophy": 2,
    "Simpson-Golabi-Behmel_syndrome_type_2": 4,
    "Intellectual_disability|Joubert_syndrome|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "Orofaciodigital_syndrome_I|OFD1-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I": 17,
    "not_provided|Orofaciodigital_syndrome_I": 4,
    "Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Joubert_syndrome|OFD1-related_disorder": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Primary_ciliary_dyskinesia": 1,
    "Retinal_dystrophy|Orofaciodigital_syndrome_I|Joubert_syndrome|OFD1-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Joubert_syndrome": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided|not_specified": 1,
    "Joubert_syndrome_10|not_provided": 2,
    "OFD1-related_disorder|Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Joubert_syndrome": 2,
    "Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Joubert_syndrome_10": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|History_of_neurodevelopmental_disorder|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "Primary_ciliary_dyskinesia|not_provided|Joubert_syndrome|Orofaciodigital_syndrome_I": 2,
    "Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided": 1,
    "OFD1-related_disorder|Simpson-Golabi-Behmel_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10|not_provided": 1,
    "OFD1-related_disorder|Joubert_syndrome|Orofaciodigital_syndrome_I|COACH_syndrome": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|Cerebral_arteriopathy|_autosomal_dominant|_with_subcortical_infarcts_and_leukoencephalopathy|_type_1": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23": 3,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|OFD1-related_disorder": 3,
    "Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Retinal_dystrophy|Joubert_syndrome": 1,
    "not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "OFD1-related_disorder|Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided|Primary_ciliary_dyskinesia": 1,
    "OFD1-related_disorder|Orofaciodigital_syndrome_I|Joubert_syndrome|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Primary_ciliary_dyskinesia": 1,
    "OFD1-related_disorder|not_provided|Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|not_provided": 1,
    "Retinitis_pigmentosa_23": 2,
    "OFD1-related_disorder|Orofaciodigital_syndrome_I|Joubert_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract|not_provided": 1,
    "Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome|not_specified": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided": 5,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified|not_provided|Primary_ciliary_dyskinesia|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Joubert_syndrome|not_provided|OFD1-related_disorder": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|not_specified|not_provided|Primary_ciliary_dyskinesia": 4,
    "Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome": 2,
    "not_provided|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Joubert_syndrome|not_specified": 1,
    "not_specified|Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia": 1,
    "not_specified|OFD1-related_disorder|Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_specified|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "not_specified|Joubert_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|not_provided": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome|not_provided|Primary_ciliary_dyskinesia": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|not_specified": 5,
    "Orofaciodigital_syndrome_I|Orofacial-digital_syndrome_III": 1,
    "OFD1-related_disorder|Orofaciodigital_syndrome_I": 1,
    "Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I|Joubert_syndrome": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Intellectual_disability|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|OFD1-related_disorder|Retinitis_pigmentosa_23|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|not_specified|not_provided|Primary_ciliary_dyskinesia|Intellectual_disability": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|OFD1-related_disorder": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided|Primary_ciliary_dyskinesia": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23": 1,
    "Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|not_provided|Retinitis_pigmentosa_23": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10": 1,
    "not_provided|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10|Joubert_syndrome": 1,
    "Primary_ciliary_dyskinesia|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I|Joubert_syndrome": 2,
    "not_specified|Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified|not_provided": 2,
    "Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2": 2,
    "Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|Primary_ciliary_dyskinesia": 1,
    "not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome|not_specified": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Kidney_failure": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|OFD1-related_disorder|not_provided|not_specified": 1,
    "Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Joubert_syndrome|not_specified": 1,
    "Congenital_cerebellar_hypoplasia|not_provided|Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome|not_specified": 1,
    "Intellectual_disability|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Retinal_dystrophy|not_provided": 2,
    "not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome|Primary_ciliary_dyskinesia|OFD1-related_disorder|Ciliopathy": 1,
    "Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I|OFD1-related_disorder": 1,
    "not_provided|Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified": 1,
    "OFD1-related_disorder|not_provided": 2,
    "Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome|Retinal_dystrophy|Primary_ciliary_dyskinesia|not_specified": 1,
    "Bifid_nail|Abnormal_nail_morphology|Ridged_nail|Polydactyly|_postaxial|_type_A1|Retinitis_pigmentosa_23": 1,
    "not_specified|Osteoporosis": 1,
    "not_provided|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23": 1,
    "Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified|not_provided": 1,
    "Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Joubert_syndrome|not_specified|not_provided": 1,
    "History_of_neurodevelopmental_disorder|Joubert_syndrome|Orofaciodigital_syndrome_I|not_provided": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided|not_specified": 1,
    "not_provided|Joubert_syndrome|Orofaciodigital_syndrome_I|Retinal_dystrophy|OFD1-related_disorder|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "OFD1-related_disorder|Joubert_syndrome|Orofaciodigital_syndrome_I|not_specified": 2,
    "Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|not_specified": 1,
    "Primary_ciliary_dyskinesia|not_provided|Orofaciodigital_syndrome_I|Joubert_syndrome": 1,
    "Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Joubert_syndrome": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 2,
    "Primary_ciliary_dyskinesia|not_provided|Joubert_syndrome|Orofaciodigital_syndrome_I|OFD1-related_disorder": 1,
    "OFD1-related_ciliopathy|not_provided": 1,
    "not_provided|Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2": 1,
    "OFD1-related_disorder|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "Primary_ciliary_dyskinesia|OFD1-related_disorder": 1,
    "not_specified|Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|not_specified|Joubert_syndrome|not_provided": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia": 1,
    "Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_23|Joubert_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "not_provided|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia|Retinal_dystrophy|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Retinal_dystrophy|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "Ventriculomegaly|Polymicrogyria|Cerebellar_vermis_hypoplasia": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Primary_ciliary_dyskinesia|OFD1-related_disorder|not_provided": 1,
    "Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "Joubert_syndrome|Orofaciodigital_syndrome_I|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|not_provided": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|OFD1-related_disorder|Joubert_syndrome": 1,
    "not_specified|Orofaciodigital_syndrome_I|Joubert_syndrome": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10": 1,
    "not_provided|Retinal_dystrophy|Primary_ciliary_dyskinesia|Joubert_syndrome|Orofaciodigital_syndrome_I": 1,
    "Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|not_specified|Joubert_syndrome|Primary_ciliary_dyskinesia": 1,
    "Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Primary_ciliary_dyskinesia": 1,
    "Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Joubert_syndrome|Primary_ciliary_dyskinesia": 1,
    "Orofaciodigital_syndrome_I|Joubert_syndrome|Joubert_syndrome_10|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Joubert_syndrome|Retinal_dystrophy": 1,
    "not_specified|Joubert_syndrome|Orofaciodigital_syndrome_I|Rare_genetic_intellectual_disability|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I|Joubert_syndrome_10|Joubert_syndrome": 1,
    "Primary_ciliary_dyskinesia|OFD1-related_disorder|Orofaciodigital_syndrome_I|Joubert_syndrome|Respiratory_ciliopathies_including_non-CF_bronchiectasis": 1,
    "Simpson-Golabi-Behmel_syndrome_type_2|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Joubert_syndrome_10|Joubert_syndrome|Primary_ciliary_dyskinesia|not_specified": 1,
    "Primary_ciliary_dyskinesia|Joubert_syndrome": 3,
    "Simpson-Golabi-Behmel_syndrome": 1,
    "Inborn_genetic_diseases|Primary_ciliary_dyskinesia|Orofaciodigital_syndrome_I|Joubert_syndrome": 1,
    "not_provided|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I": 1,
    "Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome_10|Joubert_syndrome|not_provided|not_specified": 1,
    "Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Joubert_syndrome|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|not_provided|Simpson-Golabi-Behmel_syndrome_type_2|Retinitis_pigmentosa_23|Orofaciodigital_syndrome_I|Joubert_syndrome_10": 1,
    "Primary_ciliary_dyskinesia|Joubert_syndrome_10|Orofaciodigital_syndrome_I|Retinitis_pigmentosa_23|Simpson-Golabi-Behmel_syndrome_type_2|Joubert_syndrome": 1,
    "OFD1-related_disorder|Orofaciodigital_syndrome_I|Joubert_syndrome|not_provided": 1,
    "GLRA2-related_disorder": 8,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_Pilorge_type": 10,
    "not_provided|See_cases|Intellectual_developmental_disorder|_X-linked|_syndromic|_Pilorge_type": 1,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_Pilorge_type|See_cases": 1,
    "not_provided|Intellectual_developmental_disorder|_X-linked|_syndromic|_Pilorge_type|See_cases": 1,
    "not_provided|Intellectual_developmental_disorder|_X-linked|_syndromic|_Pilorge_type|Inborn_genetic_diseases": 1,
    "not_provided|GLRA2-related_disorder": 1,
    "GLRA2-related_disorder|not_provided": 1,
    "See_cases|Intellectual_developmental_disorder|_X-linked|_syndromic|_Pilorge_type": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B": 13,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|not_provided": 1,
    "Fanconi_anemia_complementation_group_B": 48,
    "not_provided|Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "FANCB-related_disorder|not_provided|Fanconi_anemia|not_specified|Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "Fanconi_anemia|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|FANCB-related_disorder|not_provided|Fanconi_anemia_complementation_group_B|not_specified": 1,
    "not_specified|Fanconi_anemia|Fanconi_anemia_complementation_group_B|not_provided": 1,
    "Fanconi_anemia_complementation_group_B|Fanconi_anemia|FANCB-related_disorder|Inborn_genetic_diseases|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|Fanconi_anemia": 3,
    "Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia": 8,
    "Multiple_congenital_anomalies/dysmorphic_syndrome|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|not_specified|not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "FANCB-related_disorder|Fanconi_anemia": 7,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|not_provided|Fanconi_anemia_complementation_group_B|Fanconi_anemia": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|Fanconi_anemia|Inborn_genetic_diseases|FANCB-related_disorder": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_B": 13,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_B": 2,
    "Fanconi_anemia|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement|not_provided": 5,
    "Fanconi_anemia|FANCB-related_disorder|not_specified|not_provided": 2,
    "Fanconi_anemia_complementation_group_B|FANCB-related_disorder|not_provided|not_specified|History_of_neurodevelopmental_disorder|Fanconi_anemia": 1,
    "Fanconi_anemia|FANCB-related_disorder|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 2,
    "not_provided|Fanconi_anemia_complementation_group_B": 1,
    "not_provided|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia|Fanconi_anemia_complementation_group_B|not_provided": 2,
    "not_specified|not_provided|Fanconi_anemia_complementation_group_A|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Malignant_tumor_of_breast|FANCB-related_disorder|Fanconi_anemia|History_of_neurodevelopmental_disorder|Fanconi_anemia_complementation_group_B": 1,
    "Fanconi_anemia|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|not_provided": 1,
    "Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Inborn_genetic_diseases|Fanconi_anemia|FANCB-related_disorder|not_specified": 1,
    "Fanconi_anemia_complementation_group_B|Fanconi_anemia": 10,
    "Fanconi_anemia_complementation_group_B|Inborn_genetic_diseases|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_B|not_provided": 1,
    "FANCB-related_disorder|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "Fanconi_anemia|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 3,
    "Fanconi_anemia_complementation_group_B|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Inborn_genetic_diseases": 2,
    "not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "Fanconi_anemia|Glioma_susceptibility_1|Fanconi_anemia_complementation_group_B": 1,
    "FANCB-related_disorder|Fanconi_Anemia|_X-Linked|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_provided|not_specified|VACTERL_with_hydrocephalus|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "not_provided|Fanconi_anemia_complementation_group_B|X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement|not_specified|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia": 1,
    "not_provided|Fanconi_anemia_complementation_group_B|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "FANCB-related_disorder|Fanconi_anemia_complementation_group_B|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "Fanconi_anemia_complementation_group_B|FANCB-related_disorder|Fanconi_anemia": 1,
    "FANCB-related_disorder": 3,
    "not_specified|Inborn_genetic_diseases|Fanconi_anemia_complementation_group_B|Fanconi_anemia": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|not_specified|FANCB-related_disorder|Fanconi_anemia|Inborn_genetic_diseases": 1,
    "Fanconi_anemia|FANCB-related_disorder|Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|not_provided": 1,
    "Fanconi_anemia|FANCB-related_disorder|Inborn_genetic_diseases|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B": 1,
    "Fanconi_anemia_complementation_group_B|not_specified|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia|Inborn_genetic_diseases|not_provided": 1,
    "FANCB-related_disorder|not_specified|not_provided|Fanconi_anemia": 1,
    "Fanconi_anemia|Inborn_genetic_diseases|FANCB-related_disorder": 1,
    "VACTERL_with_hydrocephalus|Fanconi_Anemia|_X-Linked|Fanconi_anemia|FANCB-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "Fanconi_anemia_complementation_group_B|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 3,
    "Fanconi_anemia|Inborn_genetic_diseases|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|FANCB-related_disorder": 1,
    "not_specified|Fanconi_anemia_complementation_group_B|Fanconi_anemia|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "Fanconi_anemia|FANCB-related_disorder": 3,
    "Inborn_genetic_diseases|Fanconi_anemia|not_specified": 1,
    "not_specified|Fanconi_anemia|not_provided|FANCB-related_disorder": 1,
    "Fanconi_anemia|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B": 1,
    "Fanconi_anemia|Fanconi_anemia_complementation_group_B|Inborn_genetic_diseases": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia|Fanconi_anemia_complementation_group_B|History_of_neurodevelopmental_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Fanconi_anemia_complementation_group_B|not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia": 1,
    "Fanconi_Anemia|_X-Linked|VACTERL_with_hydrocephalus|Fanconi_anemia": 1,
    "not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|not_specified|Fanconi_anemia": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|FANCB-related_disorder": 1,
    "not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Fanconi_anemia_complementation_group_B|Fanconi_anemia": 1,
    "Fanconi_anemia_complementation_group_B|Fanconi_anemia|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "Inborn_genetic_diseases|Fanconi_anemia|Fanconi_anemia_complementation_group_B": 1,
    "X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|not_provided|Fanconi_anemia_complementation_group_B": 1,
    "not_specified|PIGA-related_disorder|not_provided": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 174,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 12,
    "Inborn_genetic_diseases|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 5,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_provided": 17,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|PIGA-related_disorder": 1,
    "Paroxysmal_nocturnal_hemoglobinuria": 9,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Paroxysmal_nocturnal_hemoglobinuria_1": 3,
    "not_provided|PIGA-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_specified": 3,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_provided|PIGA-related_disorder|Inborn_genetic_diseases": 1,
    "PIGA-related_disorder|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Inborn_genetic_diseases": 11,
    "PIGA-related_disorder": 4,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Paroxysmal_nocturnal_hemoglobinuria_1": 1,
    "Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis|not_provided": 1,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 3,
    "not_provided|not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|PIGA-related_disorder": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|PIGA-related_disorder": 2,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_provided": 1,
    "PIGA-related_disorder|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 2,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Inborn_genetic_diseases|not_provided": 3,
    "Neurodevelopmental_abnormality|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_provided": 1,
    "not_specified|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Paroxysmal_nocturnal_hemoglobinuria_1|Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis|Inborn_genetic_diseases": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis": 1,
    "Paroxysmal_nocturnal_hemoglobinuria_1|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_provided": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Paroxysmal_nocturnal_hemoglobinuria_1|not_provided": 1,
    "Paroxysmal_nocturnal_hemoglobinuria|not_provided": 1,
    "PIGA-related_disorder|Inborn_genetic_diseases|not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "Paroxysmal_nocturnal_hemoglobinuria_1|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis": 1,
    "not_provided|Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis": 1,
    "Paroxysmal_nocturnal_hemoglobinuria_1|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "not_provided|Paroxysmal_nocturnal_hemoglobinuria_1": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Neurodevelopmental_disorder_with_epilepsy_and_hemochromatosis": 1,
    "Inborn_genetic_diseases|Paroxysmal_nocturnal_hemoglobinuria_1|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "not_provided|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2": 1,
    "not_provided|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_specified": 1,
    "Multiple_congenital_anomalies-hypotonia-seizures_syndrome_2|not_provided|Inborn_genetic_diseases": 1,
    "Orofaciodigital_syndrome_21|Heart|_malformation_of|Holoprosencephaly_sequence|Median_cleft_lip_and_palate|Severe_hydrocephalus": 1,
    "Orofaciodigital_syndrome_21": 1,
    "Pettigrew_syndrome": 14,
    "Pettigrew_syndrome|not_provided": 4,
    "not_specified|Inborn_genetic_diseases|AP1S2-related_disorder|not_provided": 1,
    "AP1S2-related_disorder": 1,
    "Fried_syndrome|Pettigrew_syndrome|not_provided": 1,
    "X-linked_syndromic_intellectual_disability": 3,
    "not_provided|GRPR-related_disorder": 3,
    "GRPR-related_disorder": 2,
    "GRPR-related_disorder|not_provided": 2,
    "CYTIDINE_5-PRIME_TRIPHOSPHATE_SYNTHETASE_2_deficiency": 1,
    "Laterality_defects|_autosomal_dominant|not_specified": 2,
    "Spermatogenic_failure|_X-linked|_9": 1,
    "Nance-Horan_syndrome": 254,
    "Inborn_genetic_diseases|Nance-Horan_syndrome": 20,
    "NHS-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Nance-Horan_syndrome|Cataract_40|not_provided": 1,
    "Cataract_40|Nance-Horan_syndrome|not_specified": 1,
    "Nance-Horan_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|Nance-Horan_syndrome": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Nance-Horan_syndrome": 10,
    "NHS-related_disorder": 8,
    "Nance-Horan_syndrome|Inborn_genetic_diseases|not_provided|Cataract_40|not_specified": 1,
    "Nance-Horan_syndrome|Inborn_genetic_diseases": 23,
    "NHS-related_disorder|Inborn_genetic_diseases|not_provided|Nance-Horan_syndrome": 1,
    "not_provided|Nance-Horan_syndrome": 14,
    "NHS-related_disorder|Nance-Horan_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Nance-Horan_syndrome|not_provided": 9,
    "Inborn_genetic_diseases|Nance-Horan_syndrome|not_provided": 3,
    "not_specified|Nance-Horan_syndrome": 6,
    "Cataract_40|Inborn_genetic_diseases": 1,
    "Cataract_40": 5,
    "Cataract_40|Nance-Horan_syndrome|not_specified|not_provided": 1,
    "NHS-related_disorder|Nance-Horan_syndrome": 3,
    "not_specified|not_provided|Nance-Horan_syndrome": 1,
    "Cataract_40|Nance-Horan_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Nance-Horan_syndrome|not_specified": 1,
    "See_cases|Nance-Horan_syndrome": 1,
    "Nance-Horan_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Nance-Horan_syndrome|Inborn_genetic_diseases": 1,
    "Nance-Horan_syndrome|Congenital_ocular_coloboma": 1,
    "Nance-Horan_syndrome|Cataract_40": 3,
    "Nance-Horan_syndrome|Intellectual_disability|not_provided": 1,
    "NHS-related_disorder|not_provided|Inborn_genetic_diseases|Nance-Horan_syndrome": 1,
    "Nance-Horan_syndrome|History_of_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Nance-Horan_syndrome|Intellectual_disability": 2,
    "Cataract_40|Nance-Horan_syndrome|not_provided": 1,
    "NHS-related_disorder|Inborn_genetic_diseases|Nance-Horan_syndrome|Cataract_40": 1,
    "NHS-related_disorder|Nance-Horan_syndrome|Inborn_genetic_diseases": 1,
    "Nance-Horan_syndrome|NHS-related_disorder|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|Nance-Horan_syndrome": 4,
    "Nance-Horan_syndrome|NHS-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Nance-Horan_syndrome": 1,
    "Inborn_genetic_diseases|NHS-related_disorder|Nance-Horan_syndrome|not_provided": 1,
    "Nance-Horan_syndrome|Inborn_genetic_diseases|not_provided|NHS-related_disorder": 1,
    "Inborn_genetic_diseases|NHS-related_disorder|Nance-Horan_syndrome": 2,
    "Nance-Horan_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Prostate_cancer|Inborn_genetic_diseases|Nance-Horan_syndrome": 1,
    "NHS-related_disorder|not_provided|not_specified|Nance-Horan_syndrome|Lymphedema|Intellectual_disability": 1,
    "NHS-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Nance-Horan_syndrome|Intellectual_disability": 2,
    "Nance-Horan_syndrome|not_specified": 1,
    "Nance-Horan_syndrome|Inborn_genetic_diseases|NHS-related_disorder": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Nance-Horan_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Nance-Horan_syndrome|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Cataract_40|Nance-Horan_syndrome": 1,
    "not_specified|NHS-related_disorder|not_provided|Nance-Horan_syndrome": 1,
    "not_provided|Nance-Horan_syndrome|Inborn_genetic_diseases": 1,
    "NHS-related_disorder|not_specified|not_provided|Nance-Horan_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|NHS-related_disorder|Nance-Horan_syndrome": 1,
    "Nance-Horan_syndrome|not_specified|not_provided": 1,
    "X-linked_syndromic_intellectual_disability|Nance-Horan_syndrome": 1,
    "not_provided|Cataract_40": 1,
    "Intellectual_disability|Nance-Horan_syndrome|Inborn_genetic_diseases": 1,
    "CDKL5_disorder|not_provided|Atypical_Rett_syndrome": 1,
    "CDKL5_disorder|not_specified": 9,
    "CDKL5_disorder|not_specified|not_provided": 5,
    "CDKL5-related_disorder": 11,
    "Atypical_Rett_syndrome|CDKL5_disorder": 11,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|not_provided": 2,
    "not_specified|CDKL5-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 354,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 21,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 217,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2": 25,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder": 5,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 7,
    "not_provided|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 6,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|not_provided": 5,
    "CDKL5_disorder": 59,
    "Developmental_and_epileptic_encephalopathy|_2|not_provided|CDKL5_disorder": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 9,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder|not_specified": 2,
    "CDKL5_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_2": 6,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Angelman_syndrome-like": 5,
    "Developmental_and_epileptic_encephalopathy|_2|not_provided": 3,
    "CDKL5_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 6,
    "CDKL5_disorder|History_of_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|not_provided": 1,
    "not_provided|West_syndrome|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 1,
    "not_provided|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2": 5,
    "Developmental_and_epileptic_encephalopathy|_2|not_specified|not_provided|Angelman_syndrome-like": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Atypical_Rett_syndrome|Angelman_syndrome-like": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 1,
    "CDKL5_disorder|Atypical_Rett_syndrome|not_provided": 2,
    "not_provided|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 12,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_provided": 16,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified": 6,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Angelman_syndrome-like": 1,
    "CDKL5-related_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 2,
    "Developmental_and_epileptic_encephalopathy|_2|Rett_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder|Atypical_Rett_syndrome": 2,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|CDKL5-related_disorder|CDKL5_disorder|Atypical_Rett_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 25,
    "not_specified|CDKL5-related_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Atypical_Rett_syndrome|Autism": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder|CDKL5-related_disorder|not_specified": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 5,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Rett_syndrome": 1,
    "Atypical_Rett_syndrome|not_provided|CDKL5_disorder": 2,
    "not_provided|CDKL5_disorder": 9,
    "CDKL5_disorder|Atypical_Rett_syndrome": 7,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|Rett_syndrome|Seizure": 1,
    "CDKL5_disorder|not_provided": 6,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 21,
    "not_provided|not_specified|CDKL5_disorder": 3,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 4,
    "CDKL5_disorder|Atypical_Rett_syndrome|Developmental_and_epileptic_encephalopathy|_2": 2,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Inborn_genetic_diseases": 6,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_provided|CDKL5_disorder|Inborn_genetic_diseases": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified": 7,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|Atypical_Rett_syndrome|CDKL5-related_disorder": 1,
    "CDKL5_disorder|not_provided|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Atypical_Rett_syndrome": 1,
    "not_specified|CDKL5_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_2|West_syndrome": 1,
    "Rett_syndrome|Developmental_and_epileptic_encephalopathy|_2|not_provided": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_specified": 4,
    "not_specified|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 5,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|CDKL5_disorder|Atypical_Rett_syndrome": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2": 4,
    "not_provided|CDKL5_disorder|not_specified": 3,
    "not_specified|CDKL5_disorder|not_provided": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Inborn_genetic_diseases|not_provided": 1,
    "CDKL5_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_specified|not_provided": 1,
    "not_provided|History_of_neurodevelopmental_disorder|CDKL5-related_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "CDKL5_disorder|CDKL5-related_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder": 2,
    "Inborn_genetic_diseases|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Atypical_Rett_syndrome": 2,
    "CDKL5_disorder|Atypical_Rett_syndrome|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "Inborn_genetic_diseases|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|Atypical_Rett_syndrome|Intellectual_disability": 1,
    "CDKL5_disorder|West_syndrome|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|CDKL5_disorder|not_provided": 1,
    "not_specified|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Epileptic_encephalopathy|not_provided|CDKL5_disorder": 1,
    "Global_developmental_delay|Generalized_hypotonia|Delayed_speech_and_language_development|Stereotypic_movement_disorder|Seizure|Stereotypical_hand_wringing|Stereotypical_body_rocking|Bruxism|Developmental_and_epileptic_encephalopathy|_2": 1,
    "CDKL5_disorder|Atypical_Rett_syndrome|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Inborn_genetic_diseases|CDKL5_disorder": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "not_provided|CDKL5_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Abnormality_of_the_nervous_system|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome|CDKL5_disorder": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|Inborn_genetic_diseases": 7,
    "History_of_neurodevelopmental_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Inborn_genetic_diseases|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 3,
    "CDKL5_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|CDKL5_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|CDKL5-related_disorder": 1,
    "not_provided|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 2,
    "CDKL5_disorder|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5-related_disorder": 1,
    "CDKL5_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_2|Atypical_Rett_syndrome": 1,
    "not_provided|CDKL5_disorder|Inborn_genetic_diseases": 1,
    "CDKL5_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "Epileptic_encephalopathy|CDKL5_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|CDKL5_disorder": 1,
    "CDKL5_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|Craniosynostosis_syndrome|not_provided|CDKL5-related_disorder": 1,
    "not_provided|History_of_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_specified|Inborn_genetic_diseases": 3,
    "West_syndrome|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Atypical_Rett_syndrome": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 3,
    "CDKL5_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_2": 1,
    "not_provided|Inborn_genetic_diseases|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_provided|CDKL5_disorder": 1,
    "not_specified|not_provided|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5-related_disorder": 1,
    "Developmental_delay|Epileptic_encephalopathy": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5-related_disorder|CDKL5_disorder|Inborn_genetic_diseases|Autism|not_provided": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_specified|CDKL5_disorder|not_provided": 1,
    "CDKL5_disorder|Inborn_genetic_diseases|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5-related_disorder": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|Atypical_Rett_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Atypical_Rett_syndrome|not_provided|CDKL5_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|CDKL5-related_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Inborn_genetic_diseases": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_2|not_provided|CDKL5_disorder|Angelman_syndrome-like|not_specified": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|not_provided": 1,
    "CDKL5-related_disorder|History_of_neurodevelopmental_disorder|not_specified|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Developmental_and_epileptic_encephalopathy|_2|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Angelman_syndrome-like|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|CDKL5-related_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_provided": 1,
    "not_provided|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|Atypical_Rett_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|CDKL5_disorder": 1,
    "not_specified|not_provided|CDKL5_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Atypical_Rett_syndrome|CDKL5_disorder|Angelman_syndrome-like": 1,
    "Inborn_genetic_diseases|not_provided|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder": 1,
    "CDKL5_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_provided": 2,
    "Inborn_genetic_diseases|CDKL5_disorder": 1,
    "CDKL5_disorder|CDKL5-related_disorder|not_provided|not_specified|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_provided|not_specified": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Inborn_genetic_diseases|CDKL5-related_disorder": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|History_of_neurodevelopmental_disorder|Angelman_syndrome-like|not_specified": 1,
    "CDKL5_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_2|not_provided|CDKL5_disorder|Inborn_genetic_diseases|Angelman_syndrome-like|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|CDKL5_disorder|not_specified": 1,
    "CDKL5-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|not_specified|CDKL5_disorder": 1,
    "CDKL5-related_disorder|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified": 1,
    "CDKL5_disorder|not_specified|not_provided|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 2,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Atypical_Rett_syndrome|Angelman_syndrome-like": 1,
    "Inborn_genetic_diseases|not_provided|CDKL5_disorder|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Inborn_genetic_diseases|CDKL5_disorder|not_provided|Angelman_syndrome-like": 1,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Inborn_genetic_diseases": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|Atypical_Rett_syndrome|Seizure": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 1,
    "not_specified|not_provided|CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|not_specified|Abnormal_cerebral_morphology|CDKL5_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|CDKL5_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_2|Developmental_and_epileptic_encephalopathy|CDKL5_disorder": 1,
    "RS1-related_disorder": 1,
    "Juvenile_retinoschisis": 54,
    "not_provided|Juvenile_retinoschisis": 55,
    "Retinal_dystrophy|Juvenile_retinoschisis|not_provided": 4,
    "Retinal_dystrophy|not_provided|Juvenile_retinoschisis": 20,
    "Retinal_dystrophy|not_provided|Juvenile_retinoschisis|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Retinoschisis": 2,
    "Retinal_dystrophy|not_provided|Juvenile_retinoschisis|Retinoschisis": 3,
    "Retinal_dystrophy|not_provided|Retinoschisis": 2,
    "Juvenile_retinoschisis|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Juvenile_retinoschisis": 1,
    "Retinal_dystrophy|Juvenile_retinoschisis|not_specified|not_provided": 1,
    "Juvenile_retinoschisis|not_provided": 17,
    "not_provided|Retinoschisis": 2,
    "Retinal_dystrophy|not_specified|not_provided|Juvenile_retinoschisis": 1,
    "Inborn_genetic_diseases|not_provided|Juvenile_retinoschisis": 2,
    "not_provided|RS1-related_disorder": 2,
    "Juvenile_retinoschisis|Retinal_dystrophy": 2,
    "Retinal_dystrophy|Juvenile_retinoschisis": 2,
    "Macular_schisis|Peripheral_schisis|Juvenile_retinoschisis": 1,
    "not_provided|not_specified|Juvenile_retinoschisis": 1,
    "not_provided|Juvenile_retinoschisis|Retinoschisis": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|CDKL5-related_disorder": 1,
    "Inborn_genetic_diseases|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder": 1,
    "RS1-related_disorder|Retinal_dystrophy|not_provided|Juvenile_retinoschisis": 1,
    "Juvenile_retinoschisis|RS1-related_disorder|not_provided": 1,
    "RS1-related_disorder|Juvenile_retinoschisis|not_provided": 1,
    "Retinal_dystrophy|Inborn_genetic_diseases|not_provided|Juvenile_retinoschisis": 1,
    "not_provided|RS1-related_disorder|Retinal_dystrophy|Juvenile_retinoschisis": 1,
    "CDKL5_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided|not_specified": 1,
    "CDKL5_disorder|not_specified|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2|Inborn_genetic_diseases|not_specified": 1,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|not_provided": 3,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|not_provided|Atypical_Rett_syndrome": 1,
    "Developmental_and_epileptic_encephalopathy|_2|Developmental_and_epileptic_encephalopathy|_1|Angelman_syndrome-like": 1,
    "Developmental_and_epileptic_encephalopathy|_2|CDKL5_disorder|Angelman_syndrome-like|not_specified": 1,
    "CDKL5_disorder|Epileptic_encephalopathy|Angelman_syndrome-like|Developmental_and_epileptic_encephalopathy|_2": 1,
    "CDKL5_disorder|Inborn_genetic_diseases|not_specified": 1,
    "History_of_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|not_provided": 1,
    "CDKL5_disorder|History_of_neurodevelopmental_disorder|not_specified|West_syndrome|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_provided": 1,
    "CDKL5_disorder|History_of_neurodevelopmental_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|not_provided|CDKL5-related_disorder": 2,
    "CDKL5_disorder|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like|not_specified|CDKL5-related_disorder": 1,
    "CDKL5_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_2|Angelman_syndrome-like": 1,
    "Juvenile_retinoschisis|Retinal_dystrophy|not_provided": 2,
    "Retinoschisis|Juvenile_retinoschisis|not_provided": 1,
    "not_provided|RS1-related_disorder|Juvenile_retinoschisis": 1,
    "Glycogen_storage_disease_IXa1": 232,
    "not_provided|Glycogen_storage_disease_IXa1|not_specified": 4,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXa1": 7,
    "Glycogen_storage_disease_IXa1|not_specified|PHKA2-related_disorder": 1,
    "not_provided|Glycogen_storage_disease_IXa1": 13,
    "Glycogen_storage_disease_IXa1|not_specified": 7,
    "PHKA2-related_disorder": 11,
    "Inborn_genetic_diseases|PHKA2-related_disorder|not_specified|not_provided|Glycogen_storage_disease_IXa1": 1,
    "Glycogen_storage_disease_IXa1|PHKA2-related_disorder": 3,
    "Glycogen_storage_disease_IXa1|Inborn_genetic_diseases": 14,
    "Glycogen_storage_disease_IXa1|Glycogen_storage_disease_IXa2": 5,
    "Glycogen_storage_disease_IXa1|not_provided": 8,
    "not_specified|Glycogen_storage_disease_IXa1": 8,
    "Glycogen_storage_disease_IXa2": 2,
    "Glycogen_storage_disease_IXa1|Inborn_genetic_diseases|not_provided": 1,
    "Aland_island_eye_disease": 9,
    "not_specified|not_provided|Glycogen_storage_disease_IXa1": 2,
    "not_specified|Glycogen_storage_disease_IXa1|PHKA2-related_disorder": 2,
    "not_provided|not_specified|Glycogen_storage_disease_IXa1": 3,
    "Glycogen_storage_disease_IXa1|not_specified|PHKA2-related_disorder|not_provided": 1,
    "PHKA2-related_disorder|Glycogen_storage_disease_IXa1": 5,
    "Glycogen_phosphorylase_kinase_deficiency|Glycogen_storage_disease_IXa1|not_provided": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXa1|not_provided": 2,
    "Intellectual_disability|Glycogen_storage_disease_IXa1": 1,
    "PHKA2-related_disorder|not_specified|Glycogen_storage_disease_IXa1": 2,
    "Glycogen_storage_disease_IXa1|not_specified|not_provided": 7,
    "Glycogen_storage_disease_IXa1|See_cases": 1,
    "Glycogen_storage_disease_IXa1|PHKA2-related_disorder|not_provided": 2,
    "not_specified|Glycogen_storage_disease_IXa1|Glycogen_phosphorylase_kinase_deficiency|not_provided": 1,
    "Glycogen_storage_disease_IXa1|not_provided|not_specified": 2,
    "Genetic_developmental_and_epileptic_encephalopathy|not_provided|Glycogen_storage_disease_IXa1": 1,
    "Inborn_genetic_diseases|not_specified|Glycogen_storage_disease_IXa1": 2,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXa1|PHKA2-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|Glycogen_storage_disease_IXa1|PHKA2-related_disorder|not_provided": 1,
    "Glycogen_storage_disease_IXa1|Inborn_genetic_diseases|not_specified": 1,
    "Glycogen_storage_disease_IXa1|not_provided|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disease_IXa1|not_provided|PHKA2-related_disorder": 1,
    "PHKA2-related_disorder|not_provided": 1,
    "not_provided|Increased_hepatic_glycogen_content|Glycogen_storage_disease_IXa1": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXa1|Glycogen_storage_disease_IXd": 1,
    "Glycogen_phosphorylase_kinase_deficiency|Glycogen_storage_disease_IXa1": 1,
    "not_specified|Glycogen_storage_disease_IXa1|not_provided": 1,
    "not_provided|Glycogen_storage_disease_IXa1|Glycogen_storage_disease_IXa2": 1,
    "Glycogen_storage_disease_IXa1|PHKA2-related_disorder|not_specified": 1,
    "PHKA2-related_disorder|not_specified": 1,
    "PHKA2-related_disorder|Glycogen_phosphorylase_kinase_deficiency|not_provided|Glycogen_storage_disease_IXa1": 1,
    "Vas_deferens|_congenital_bilateral_aplasia_of|_X-linked|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 3,
    "ADGRG2-related_disorder": 5,
    "Vas_deferens|_congenital_bilateral_aplasia_of|_X-linked": 4,
    "ADGRG2-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation": 1,
    "Congenital_bilateral_aplasia_of_vas_deferens_from_CFTR_mutation|not_provided": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|not_provided": 16,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Inborn_genetic_diseases": 4,
    "not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 36,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Seizure|Epileptic_encephalopathy": 1,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|PDHA1-related_disorder|Pyruvate_dehydrogenase_E1-alpha_deficiency|Inborn_genetic_diseases": 1,
    "See_cases|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|not_specified": 5,
    "not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency|Pyruvate_dehydrogenase_complex_deficiency": 3,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Inborn_genetic_diseases|Abnormality_of_the_mitochondrion|Pyruvate_dehydrogenase_complex_deficiency|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases": 1,
    "PDHA1-related_disorder": 7,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|not_specified|not_provided": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Neurodevelopmental_delay": 1,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency": 3,
    "Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases|PDHA1-related_disorder|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "not_provided|not_specified|Pyruvate_dehydrogenase_E1-alpha_deficiency": 2,
    "not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency|not_specified": 2,
    "not_specified|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 3,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency": 2,
    "not_specified|Pyruvate_dehydrogenase_E1-alpha_deficiency": 6,
    "Pyruvate_dehydrogenase_complex_deficiency|not_provided|Inborn_genetic_diseases|not_specified|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency": 4,
    "not_provided|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-alpha_deficiency|PDHA1-related_disorder": 1,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-alpha_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Pyruvate_dehydrogenase_complex_deficiency|not_provided": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Inborn_genetic_diseases|Pyruvate_dehydrogenase_complex_deficiency|not_specified|not_provided": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "PDHA1-related_disorder|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|PDHA1-related_disorder": 1,
    "Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Pyruvate_dehydrogenase_complex_deficiency": 4,
    "Pyruvate_dehydrogenase_complex_deficiency|not_provided|not_specified": 1,
    "PDHA1-related_disorder|Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Inborn_genetic_diseases|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency": 2,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Inborn_genetic_diseases|not_specified|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "not_specified|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases|PDHA1-related_disorder|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency|See_cases": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_complex_deficiency|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Pyruvate_dehydrogenase_complex_deficiency": 1,
    "not_provided|not_specified|Pyruvate_dehydrogenase_complex_deficiency|Inborn_genetic_diseases|Pyruvate_dehydrogenase_E1-alpha_deficiency": 1,
    "not_provided|Pyruvate_dehydrogenase_E1-alpha_deficiency|MAP3K15-related_disorder": 1,
    "Pyruvate_dehydrogenase_E1-alpha_deficiency|MAP3K15-related_disorder|not_provided": 1,
    "MAP3K15-related_disorder": 32,
    "not_specified|MAP3K15-related_disorder": 2,
    "not_provided|MAP3K15-related_disorder": 2,
    "MAP3K15-related_disorder|not_specified": 1,
    "not_provided|SH3KBP1-related_disorder": 4,
    "SH3KBP1-related_disorder|not_provided": 2,
    "Immunodeficiency_61|SH3KBP1-related_disorder|not_provided": 1,
    "not_provided|Laterality_defects|_autosomal_dominant": 1,
    "SH3KBP1-related_disorder": 3,
    "not_provided|not_specified|SH3KBP1-related_disorder": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|RPS6KA3-related_disorder": 5,
    "Coffin-Lowry_syndrome": 55,
    "Inborn_genetic_diseases|not_provided|Coffin-Lowry_syndrome|Intellectual_disability": 1,
    "Coffin-Lowry_syndrome|not_provided|Intellectual_disability|_X-linked_19": 2,
    "Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome": 104,
    "RPS6KA3-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_specified|not_provided|Intellectual_disability": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 45,
    "Intellectual_disability|_X-linked_19": 12,
    "RPS6KA3-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_provided": 1,
    "RPS6KA3-related_disorder": 36,
    "Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_provided": 7,
    "Global_developmental_delay|Coffin-Lowry_syndrome": 1,
    "not_provided|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome": 3,
    "RPS6KA3-related_disorder|RP56KA3-related_disorder": 1,
    "RPS6KA3-related_disorder|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 6,
    "not_provided|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 2,
    "Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_provided|not_specified|Inborn_genetic_diseases|RPS6KA3-related_disorder": 1,
    "not_provided|RPS6KA3-related_disorder": 2,
    "not_provided|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|RPS6KA3-related_disorder": 1,
    "RPS6KA3-related_disorder|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome": 5,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome": 2,
    "Coffin-Lowry_syndrome|not_provided|RPS6KA3-related_disorder": 1,
    "Global_developmental_delay|Motor_delay|Hypotonia|Thick_vermilion_border|Macrocephaly|Dolichocephaly|Delayed_speech_and_language_development|Inborn_genetic_diseases": 1,
    "Coffin-Lowry_syndrome|not_provided": 1,
    "not_provided|RPS6KA3-related_disorder|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 2,
    "Inborn_genetic_diseases|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 2,
    "RPS6KA3-related_disorder|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_provided": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|RPS6KA3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_provided": 5,
    "RPS6KA3-related_disorder|Intellectual_disability|_X-linked_19": 2,
    "RPS6KA3-related_disorder|Inborn_genetic_diseases|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 1,
    "Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|Inborn_genetic_diseases|not_provided|RPS6KA3-related_disorder": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|Inborn_genetic_diseases": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Coffin-Lowry_syndrome": 1,
    "Inborn_genetic_diseases|RPS6KA3-related_disorder": 1,
    "Coffin-Lowry_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|RPS6KA3-related_disorder": 1,
    "Inborn_genetic_diseases|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_provided|not_specified": 1,
    "Abnormality_of_the_lower_limb|Specific_learning_disability|Triangular_face|Mitral_valve_prolapse|Deep_philtrum|Ventricular_septal_defect|Clinodactyly|Hypertelorism|Thoracolumbar_scoliosis|Low-set_ears|Low_anterior_hairline|Gastroesophageal_reflux|Low_posterior_hairline|Micrognathia": 1,
    "not_provided|Coffin-Lowry_syndrome": 2,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|Hirsutism|Motor_delay": 1,
    "Intellectual_disability|Coffin-Lowry_syndrome|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Coffin-Lowry_syndrome": 1,
    "RPS6KA3-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_provided|RPS6KA3-related_disorder": 1,
    "RPS6KA3-related_disorder|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_provided|RPS6KA3-related_disorder|not_specified": 1,
    "not_specified|not_provided|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19": 1,
    "Inborn_genetic_diseases|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_19|Coffin-Lowry_syndrome|not_specified|not_provided": 1,
    "RPS6KA3-related_disorder|Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_provided": 1,
    "Coffin-Lowry_syndrome|Intellectual_disability|_X-linked_19|not_specified": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Houge_type": 43,
    "CNKSR2-related_disorder|not_provided": 2,
    "CNKSR2-related_disorder": 5,
    "not_provided|Intellectual_disability|_X-linked|_syndromic|_Houge_type": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked|_syndromic|_Houge_type": 1,
    "X-linked_recessive_seizure_and_neurodevelopmental_deficit": 1,
    "not_specified|Intellectual_disability|_X-linked|_syndromic|_Houge_type": 1,
    "not_provided|CNKSR2-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked|_syndromic|_Houge_type|not_provided": 1,
    "Inborn_genetic_diseases|CNKSR2-related_disorder": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Houge_type|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Houge_type|not_provided": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Houge_type|Inborn_genetic_diseases|CNKSR2-related_disorder": 1,
    "Hearing_loss|_X-linked_4": 19,
    "not_provided|Myopathy|_distal|_7|_adult-onset|_X-linked": 1,
    "not_provided|Hearing_loss|_X-linked_4|SMPX-related_disorder": 1,
    "SMPX-related_disorder": 1,
    "X-linked_deafness": 1,
    "Myopathy|_distal|_7|_adult-onset|_X-linked": 3,
    "MBTPS2-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome": 1,
    "not_provided|Olmsted_syndrome|_X-linked": 1,
    "Osteogenesis_imperfecta|_type_19": 3,
    "Inborn_genetic_diseases|Skeletal_dysplasia|MBTPS2-related_disorder|not_specified|not_provided": 1,
    "IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome": 6,
    "not_provided|MBTPS2-related_disorder": 1,
    "IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome|MBTPS2-related_disorder": 1,
    "Olmsted_syndrome|_X-linked|Keratosis_follicularis_spinulosa_decalvans|_X-linked|IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome|MBTPS2-related_disorder|Osteogenesis_imperfecta|_type_19": 1,
    "not_provided|IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome": 3,
    "IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome|Keratosis_follicularis_spinulosa_decalvans|_X-linked|Osteogenesis_imperfecta|_type_19|Olmsted_syndrome|_X-linked": 1,
    "MBTPS2-related_disorder": 2,
    "Inborn_genetic_diseases|Osteogenesis_imperfecta|MBTPS2-related_disorder|not_provided|Intellectual_disability": 1,
    "Olmsted_syndrome|_X-linked": 1,
    "Olmsted_syndrome|_X-linked|Osteogenesis_imperfecta|_type_19|IFAP_syndrome_1|_with_or_without_BRESHECK_syndrome|Keratosis_follicularis_spinulosa_decalvans|_X-linked": 1,
    "Keratosis_follicularis_spinulosa_decalvans|_X-linked|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Snyder_type": 24,
    "SMS-related_disorder": 9,
    "SMS-related_disorder|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_Snyder_type|not_provided|Inborn_genetic_diseases": 2,
    "Syndromic_X-linked_intellectual_disability_Snyder_type|not_provided": 4,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Snyder_type|not_provided": 2,
    "not_provided|Syndromic_X-linked_intellectual_disability_Snyder_type": 3,
    "not_provided|SMS-related_disorder|Inborn_genetic_diseases": 1,
    "SMS-related_disorder|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Snyder_type|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|SMS-related_disorder": 1,
    "not_specified|not_provided|Syndromic_X-linked_intellectual_disability_Snyder_type|Inborn_genetic_diseases|SMS-related_disorder": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 211,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided": 74,
    "not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 102,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|PHEX-related_disorder|not_specified": 1,
    "not_specified|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|PHEX-related_disorder|Hypophosphatemic_rickets": 1,
    "not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_specified": 1,
    "PHEX-related_disorder|not_provided": 3,
    "PHEX-related_disorder": 8,
    "not_provided|Inborn_genetic_diseases|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 2,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|not_specified": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|Inborn_genetic_diseases|not_provided": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_specified|not_provided": 3,
    "not_provided|not_specified|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 2,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|PHEX-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hypophosphatemic_rickets": 4,
    "not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|PHEX-related_disorder": 2,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|Hypophosphatemic_rickets|not_provided": 2,
    "PHEX-related_disorder|not_provided|not_specified|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|PHEX-related_disorder": 1,
    "not_specified|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|Inborn_genetic_diseases": 1,
    "PHEX-related_disorder|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided": 1,
    "not_provided|PHEX-related_disorder": 5,
    "Hypophosphatemia": 1,
    "Hypophosphatemic_rickets|not_provided": 1,
    "not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "not_provided|not_specified|PHEX-related_disorder": 1,
    "not_provided|Hypophosphatemic_rickets|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 2,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|Hypophosphatemic_rickets": 1,
    "Vitamin_D-dependent_rickets|_type_2|not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|Hypophosphatemic_rickets": 1,
    "not_provided|PHEX-related_disorder|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "Lower_limb_pain|Bowing_of_the_legs|Hypophosphatemic_rickets": 1,
    "Hypophosphatemic_rickets|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "PHEX-related_disorder|not_specified|not_provided|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|Autosomal_dominant_hypophosphatemic_rickets": 1,
    "Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|PHEX-related_disorder": 1,
    "not_specified|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|not_provided|PHEX-related_disorder": 1,
    "not_provided|DDX53-related_disorder": 2,
    "DDX53-related_disorder|not_provided": 3,
    "DDX53-related_disorder": 10,
    "not_specified|DDX53-related_disorder": 1,
    "DDX53-related_disorder|not_specified|not_provided": 1,
    "not_provided|DDX53-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Autism|_susceptibility_to|_X-linked_4": 1,
    "Inborn_genetic_diseases|Autism|_susceptibility_to|_X-linked_4|not_provided": 1,
    "PTCHD1-related_neurodevelopmental_disorder": 1,
    "PTCHD1-related_disorder|Inborn_genetic_diseases|Autism|_susceptibility_to|_X-linked_4|not_specified|not_provided": 1,
    "Autism|_susceptibility_to|_X-linked_4|not_provided|Abnormal_brain_morphology": 1,
    "PTCHD1-related_disorder": 9,
    "Autism|_susceptibility_to|_X-linked_4|Intellectual_disability": 1,
    "PTCHD1-related_disorder|Inborn_genetic_diseases": 2,
    "Autism|_susceptibility_to|_X-linked_4|Inborn_genetic_diseases": 1,
    "not_provided|Autism|_susceptibility_to|_X-linked_4": 1,
    "Non-syndromic_X-linked_intellectual_disability": 34,
    "not_provided|Inborn_genetic_diseases|PTCHD1-related_disorder": 1,
    "PTCHD1-related_autism_and_intellectual_disability": 1,
    "APOO-related_disorder": 2,
    "Cognitive_impairment_and_autistic_features|X-\u00adlinked_recessive_mitochondrial_myopathy|Lactic_acidosis|not_provided": 1,
    "KLHL15-related_disorder": 5,
    "not_provided|KLHL15-related_disorder": 1,
    "Intellectual_disability|_X-linked_103": 13,
    "MEHMO_syndrome": 17,
    "not_specified|not_provided|MEHMO_syndrome": 1,
    "EIF2S3-related_disorder": 1,
    "EIF2S3-related_disorder|not_specified|not_provided": 1,
    "not_provided|EIF2S3-related_disorder": 1,
    "not_provided|MEHMO_syndrome": 3,
    "Intellectual_developmental_disorder|_X-linked|_syndromic_37": 7,
    "not_provided|Intellectual_developmental_disorder|_X-linked|_syndromic_37": 2,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6": 140,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_specified": 7,
    "PDK3-related_disorder|Charcot-Marie-Tooth_disease_X-linked_dominant_6": 1,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_6": 4,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_provided": 1,
    "PDK3-related_disorder": 1,
    "not_specified|Charcot-Marie-Tooth_disease_X-linked_dominant_6": 7,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_provided": 4,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_6": 1,
    "not_provided|not_specified|PDK3-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_6": 1,
    "not_specified|Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_provided": 1,
    "not_specified|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_specified": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_6|not_provided|not_specified": 1,
    "POLA1-related_disorder": 7,
    "X-linked_intellectual_disability|_van_Esch_type": 12,
    "POLA1-related_disorder|not_provided": 8,
    "X-linked_reticulate_pigmentary_disorder": 2,
    "X-linked_intellectual_disability|_van_Esch_type|not_provided": 3,
    "not_provided|X-linked_reticulate_pigmentary_disorder": 2,
    "POLA1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|X-linked_reticulate_pigmentary_disorder|X-linked_intellectual_disability|_van_Esch_type": 1,
    "not_provided|X-linked_intellectual_disability|_van_Esch_type": 3,
    "Inborn_genetic_diseases|not_provided|X-linked_intellectual_disability|_van_Esch_type": 1,
    "X-linked_reticulate_pigmentary_disorder|not_provided": 1,
    "not_provided|X-linked_intellectual_disability|_van_Esch_type|X-linked_reticulate_pigmentary_disorder": 1,
    "X-linked_intellectual_disability|_van_Esch_type|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|POLA1-related_disorder": 4,
    "not_provided|not_specified|X-linked_reticulate_pigmentary_disorder": 1,
    "POLA1-related_disorder|X-linked_intellectual_disability|_van_Esch_type|not_provided": 1,
    "not_provided|Agammaglobulinemia": 1,
    "POLA1-related_disorder|X-linked_reticulate_pigmentary_disorder|X-linked_intellectual_disability|_van_Esch_type|not_provided": 1,
    "not_provided|POLA1-related_disorder|Inborn_genetic_diseases": 1,
    "X-linked_intellectual_disability|_van_Esch_type|X-linked_reticulate_pigmentary_disorder": 1,
    "X-linked_reticulate_pigmentary_disorder|X-linked_intellectual_disability|_van_Esch_type|not_provided": 1,
    "not_provided|X-linked_reticulate_pigmentary_disorder|X-linked_intellectual_disability|_van_Esch_type|POLA1-related_disorder": 1,
    "ARX-related_disorder": 10,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 232,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_specified|not_provided": 2,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 219,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 20,
    "not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 11,
    "Corpus_callosum_agenesis-abnormal_genitalia_syndrome|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided": 16,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 5,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_specified": 4,
    "not_specified|Intellectual_disability|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 10,
    "Hydranencephaly_with_abnormal_genitalia": 2,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided": 19,
    "epileptic_encephalopathy|_early_infanitle|_1": 5,
    "not_specified|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 3,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|ARX-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided|Inborn_genetic_diseases|ARX-related_disorder": 1,
    "ARX-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "ARX-related_disorder|not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Partington_syndrome": 2,
    "not_provided|X-linked_lissencephaly_with_abnormal_genitalia": 2,
    "not_specified|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia": 30,
    "Developmental_and_epileptic_encephalopathy|_1|X-linked_lissencephaly_with_abnormal_genitalia": 1,
    "not_provided|ARX-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|X-linked_lissencephaly_with_abnormal_genitalia|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Partington_syndrome|Inborn_genetic_diseases": 1,
    "X-linked_spasticity-intellectual_disability-epilepsy_syndrome": 1,
    "epileptic_encephalopathy|_early_infanitle|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Ventriculomegaly": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases": 6,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_specified": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|ARX-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1": 1,
    "not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|ARX-related_disorder": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|epileptic_encephalopathy|_early_infanitle|_1": 1,
    "not_specified|not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_specified": 7,
    "ARX-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases|X-linked_lissencephaly_with_abnormal_genitalia|Partington_syndrome|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 2,
    "not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 2,
    "Developmental_and_epileptic_encephalopathy|_1|not_provided|not_specified|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_specified|Inborn_genetic_diseases": 1,
    "ARX-associated_condition": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|X-linked_lissencephaly_with_abnormal_genitalia|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Partington_syndrome": 1,
    "not_provided|Corpus_callosum_agenesis-abnormal_genitalia_syndrome": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Periventricular_heterotopia|Arachnoid_cyst|Corpus_callosum|_agenesis_of|not_provided": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Partington_syndrome": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|ARX-related_disorder|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|ARX-related_epileptic_encephalopathy": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 5,
    "not_provided|Inborn_genetic_diseases|ARX-related_disorder|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|Developmental_and_epileptic_encephalopathy|_1|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Partington_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "ARX-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_specified|not_provided": 1,
    "Seizure|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "X-linked_lissencephaly_with_abnormal_genitalia|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 7,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 3,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|ARX-related_disorder|not_specified": 1,
    "Intellectual_disability|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Muscular_dystrophy-dystroglycanopathy_(congenital_with_brain_and_eye_anomalies)|_type_A6": 1,
    "not_specified|epileptic_encephalopathy|_early_infanitle|_1": 1,
    "not_provided|Partington_syndrome": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided|epileptic_encephalopathy|_early_infanitle|_1": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Inborn_genetic_diseases|ARX-related_disorder|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Inborn_genetic_diseases|ARX-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|ARX-related_disorder": 1,
    "See_cases|Inborn_genetic_diseases|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Partington_syndrome|X-linked_lissencephaly_with_abnormal_genitalia": 1,
    "Inborn_genetic_diseases|ARX-related_disorder|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Partington_syndrome|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided|Partington_syndrome": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|History_of_neurodevelopmental_disorder|not_specified|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases": 1,
    "ARX-related_disorder|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|ARX-related_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|West_syndrome|Inborn_genetic_diseases|X-linked_lissencephaly_with_abnormal_genitalia|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Partington_syndrome|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|X-linked_lissencephaly_with_abnormal_genitalia": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|ARX-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Developmental_and_epileptic_encephalopathy|_1|Partington_syndrome|X-linked_lissencephaly_with_abnormal_genitalia": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided|epileptic_encephalopathy|_early_infanitle|_1|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related": 1,
    "not_provided|Partington_syndrome|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|X-linked_lissencephaly_with_abnormal_genitalia": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|Developmental_and_epileptic_encephalopathy|_1|X-linked_lissencephaly_with_abnormal_genitalia|Partington_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|ARX-related_disorder|not_provided|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1": 1,
    "Aicardi_syndrome": 1,
    "not_specified|Partington_syndrome|Developmental_and_epileptic_encephalopathy|_1|Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Corpus_callosum_agenesis-abnormal_genitalia_syndrome|X-linked_lissencephaly_with_abnormal_genitalia|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_or_without_seizures|_ARX-related|Developmental_and_epileptic_encephalopathy|_1|not_provided|not_specified": 1,
    "Abnormal_synaptic_transmission": 1,
    "Intellectual_disability|_X-linked_21": 31,
    "Intellectual_disability|_X-linked_21|not_provided": 9,
    "not_specified|not_provided|Intellectual_disability|_X-linked_21": 1,
    "History_of_neurodevelopmental_disorder|Intellectual_disability|_X-linked_21|not_provided": 1,
    "not_specified|Intellectual_disability|_X-linked_21|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked_21": 4,
    "IL1RAPL1-related_disorder|not_provided|Intellectual_disability|_X-linked_21": 1,
    "not_provided|IL1RAPL1-related_disorder": 2,
    "IL1RAPL1-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_21|IL1RAPL1-related_disorder": 1,
    "Intellectual_disability|_X-linked_21|not_provided|not_specified": 1,
    "IL1RAPL1-related_disorder": 3,
    "Intellectual_disability|_X-linked_21|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_21|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Intellectual_disability|_X-linked_21|Inborn_genetic_diseases": 1,
    "Congenital_adrenal_hypoplasia|_X-linked": 66,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2": 82,
    "not_specified|not_provided|NR0B1-related_disorder|Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2": 1,
    "46|XY_sex_reversal_2|Congenital_adrenal_hypoplasia|_X-linked": 146,
    "not_specified|NR0B1-related_disorder|Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2": 1,
    "Inborn_genetic_diseases|Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2": 7,
    "Congenital_adrenal_hypoplasia|_X-linked|NR0B1-related_disorder": 1,
    "not_provided|Congenital_adrenal_hypoplasia|_X-linked": 3,
    "46|XY_sex_reversal_2|Congenital_adrenal_hypoplasia|_X-linked|Inborn_genetic_diseases": 6,
    "NR0B1-related_disorder": 8,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|not_provided|not_specified": 2,
    "46|XY_sex_reversal_2|Congenital_adrenal_hypoplasia|_X-linked|not_provided": 1,
    "Congenital_adrenal_hypoplasia|_X-linked|not_provided": 2,
    "not_provided|Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2": 3,
    "not_provided|46|XY_sex_reversal_2|Congenital_adrenal_hypoplasia|_X-linked": 1,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|not_provided": 3,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|not_provided|NR0B1-related_disorder": 1,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|Inborn_genetic_diseases": 2,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|NR0B1-related_disorder": 1,
    "NR0B1-related_disorder|Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|not_specified|not_provided": 1,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|not_specified": 2,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|Mineralocorticoid_deficiency|_isolated": 1,
    "Inborn_genetic_diseases|46|XY_sex_reversal_2|Congenital_adrenal_hypoplasia|_X-linked": 1,
    "Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2|not_specified|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Congenital_adrenal_hypoplasia|_X-linked|46|XY_sex_reversal_2": 1,
    "GK-related_disorder|not_provided": 2,
    "GK-related_disorder": 3,
    "not_provided|Inborn_glycerol_kinase_deficiency": 1,
    "Inborn_genetic_diseases|Inborn_glycerol_kinase_deficiency": 1,
    "not_provided|GK-related_disorder": 1,
    "Inborn_glycerol_kinase_deficiency": 13,
    "Inborn_genetic_diseases|GK-related_disorder": 1,
    "not_provided|GK-related_disorder|History_of_neurodevelopmental_disorder": 1,
    "History_of_neurodevelopmental_disorder|not_provided|not_specified": 1,
    "not_provided|GK-related_disorder|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Absent_speech|Seizure": 1,
    "not_provided|Dilated_cardiomyopathy_3B": 9,
    "Dilated_cardiomyopathy_3B|not_provided": 5,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 559,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 11,
    "not_specified|DMD-related_disorder|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "DMD-related_disorder|Primary_familial_dilated_cardiomyopathy|not_provided|not_specified|Duchenne_muscular_dystrophy|Intellectual_disability": 1,
    "not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 6,
    "not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 2,
    "not_provided|Duchenne_muscular_dystrophy": 276,
    "Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 5,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy": 67,
    "Becker_muscular_dystrophy": 97,
    "Duchenne_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 3,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 2,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 4,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 29,
    "DMD-related_disorder": 17,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 179,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy": 32,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency": 21,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 5,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy": 6,
    "not_provided|Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 36,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 8,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy": 49,
    "not_specified|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 5,
    "Cardiovascular_phenotype|not_specified|Duchenne_muscular_dystrophy|not_provided": 2,
    "Duchenne_muscular_dystrophy|not_provided": 230,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided": 4,
    "not_provided|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 18,
    "not_specified|not_provided|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 4,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency": 3,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype": 3,
    "not_provided|DMD-related_disorder|Cardiovascular_phenotype|not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 157,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype": 8,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 9,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 56,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|Duchenne_muscular_dystrophy": 28,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy": 17,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy": 10,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|not_provided": 2,
    "not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 6,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 23,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 11,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 14,
    "not_specified|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Dystrophin_deficiency": 1,
    "not_specified|Duchenne_muscular_dystrophy": 44,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 11,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy": 13,
    "not_provided|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 14,
    "not_provided|Cardiovascular_phenotype|DMD-related_disorder|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 4,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 3,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided": 3,
    "not_specified|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 13,
    "not_provided|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 5,
    "not_provided|not_specified|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency": 17,
    "not_provided|Dystrophin_deficiency|Duchenne_muscular_dystrophy": 1,
    "not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype": 5,
    "Dilated_cardiomyopathy_3B|DMD-related_disorder": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_specified": 6,
    "not_provided|Duchenne_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 1,
    "not_specified|not_provided|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "not_provided|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 3,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Pectus_excavatum|Cardiomyopathy|Ptosis|Proptosis|Clinodactyly_of_the_5th_finger": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 19,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Primary_dilated_cardiomyopathy": 1,
    "not_provided|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|Duchenne_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|DMD-related_disorder": 1,
    "Cardiovascular_phenotype|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|not_provided|Intermediate_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 14,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 5,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Cardiovascular_phenotype": 3,
    "Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy|Abnormality_of_the_musculature|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype": 3,
    "X-linked_DMD-related_dystrophinopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|not_provided|Abnormality_of_the_musculature|See_cases": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 5,
    "Calf_muscle_hypertrophy|Proximal_muscle_weakness_in_lower_limbs|Motor_delay|not_provided|Duchenne_muscular_dystrophy": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided": 4,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|not_specified": 9,
    "not_provided|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy": 27,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 15,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|not_provided": 11,
    "Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 9,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B": 6,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_specified": 7,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 10,
    "See_cases|Becker_muscular_dystrophy": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified": 3,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 18,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|not_provided": 4,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 3,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_3B|DMD-related_disorder|Primary_dilated_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy": 19,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|Dilated_cardiomyopathy_3B|not_provided": 2,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 14,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Duchenne_muscular_dystrophy": 5,
    "not_provided|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy": 1,
    "Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 3,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|not_specified": 41,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|not_provided": 5,
    "DMD-related_disorder|not_provided|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 2,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 3,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|not_specified": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|DMD-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 18,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "not_provided|Dystrophin_deficiency": 2,
    "Duchenne_muscular_dystrophy|not_provided|DMD-related_disorder": 1,
    "not_specified|not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided": 3,
    "Cardiovascular_phenotype|Primary_familial_dilated_cardiomyopathy|not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided": 9,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Muscular_dystrophy": 1,
    "not_provided|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 3,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified": 2,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|not_provided|Duchenne_muscular_dystrophy": 2,
    "not_provided|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy": 4,
    "DMD-related_disorder|not_specified|not_provided": 2,
    "DMD-related_disorder|not_specified": 2,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Elevated_circulating_creatine_kinase_concentration|not_provided": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|not_specified|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_provided|Duchenne_muscular_dystrophy|Intellectual_disability|Cardiovascular_phenotype": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Becker_muscular_dystrophy": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 24,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided": 4,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified": 3,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 11,
    "not_specified|not_provided|Duchenne_muscular_dystrophy": 6,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|DMD-related_disorder": 2,
    "not_provided|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|not_provided": 2,
    "Duchenne_muscular_dystrophy|DMD-related_disorder": 5,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Familial_restrictive_cardiomyopathy": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 6,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 5,
    "not_provided|Cardiovascular_phenotype|DMD-related_disorder|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided": 1,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 7,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy": 5,
    "Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 2,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|DMD-related_disorder|not_specified|not_provided": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "not_specified|Duchenne_muscular_dystrophy|not_provided": 8,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Progressive_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 4,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|DMD-related_disorder|not_provided": 1,
    "not_provided|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 2,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided|not_specified": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 8,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided": 4,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiovascular_phenotype|DMD-related_disorder|not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 3,
    "Duchenne_muscular_dystrophy|Hereditary_skeletal_muscle_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_specified|not_provided": 1,
    "not_provided|Becker_muscular_dystrophy": 4,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Duchenne_muscular_dystrophy": 2,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided": 1,
    "Duchenne_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|not_provided": 2,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided": 3,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|not_specified|DMD-related_disorder": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 2,
    "Duchenne_and_Becker_muscular_dystrophy": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype": 2,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 4,
    "not_provided|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy": 4,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency": 5,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|not_provided": 3,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|not_specified|not_provided": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|not_specified|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Abnormality_of_neuronal_migration|not_provided": 1,
    "DMD-related_disorder|Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy|not_specified": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|not_specified": 6,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided": 3,
    "not_provided|Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 3,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Duchenne_muscular_dystrophy": 4,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Duchenne_muscular_dystrophy": 5,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|not_specified": 3,
    "Cardiovascular_phenotype|DMD-related_disorder|Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_specified|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Heart_failure|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "not_specified|DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 3,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|Conduction_disorder_of_the_heart|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 3,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|not_provided": 2,
    "Duchenne_muscular_dystrophy|not_specified|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy": 1,
    "Progressive_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_specified": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Primary_dilated_cardiomyopathy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Duchenne_muscular_dystrophy|not_specified|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 3,
    "not_provided|Duchenne_muscular_dystrophy|not_specified": 4,
    "not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B": 3,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|Duchenne_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy": 5,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 3,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|not_provided|Primary_familial_dilated_cardiomyopathy|Dilated_cardiomyopathy_3B": 1,
    "not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 2,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|DMD-related_disorder|not_specified|not_provided|Dilated_cardiomyopathy_3B": 3,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Duchenne_muscular_dystrophy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 5,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided|Primary_dilated_cardiomyopathy|Muscular_dystrophy": 1,
    "not_specified|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy": 2,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_specified": 2,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided|DMD-related_disorder|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_3B|not_provided": 3,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Duchenne_muscular_dystrophy|not_provided|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Duchenne_muscular_dystrophy|not_provided|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Duchenne_muscular_dystrophy": 4,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified": 2,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Dilated_cardiomyopathy_3B": 3,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B": 2,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 3,
    "Elevated_circulating_creatine_kinase_concentration|Progressive_proximal_muscle_weakness": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified": 2,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 2,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy": 8,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 17,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy": 5,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 1,
    "not_provided|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiovascular_phenotype|Hereditary_skeletal_muscle_disorder|not_specified|not_provided|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|Duchenne_and_Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B": 3,
    "not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_specified|not_provided": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Dilated_cardiomyopathy_3B|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 6,
    "DMD-related_disorder|not_provided|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_1A|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B": 3,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy": 1,
    "Dystrophin_deficiency|not_provided|Duchenne_muscular_dystrophy": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided|Cardiomyopathy|Dystrophin_deficiency": 1,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided": 2,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 7,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy": 1,
    "Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "not_specified|Dilated_cardiomyopathy_3B|Dystrophin_deficiency|not_provided|Duchenne_muscular_dystrophy": 1,
    "not_specified|DMD-related_disorder|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 2,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|DMD-related_disorder|not_specified|not_provided": 1,
    "not_provided|not_specified|Duchenne_muscular_dystrophy": 4,
    "DMD-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|not_provided": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy": 4,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 5,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|not_provided": 3,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 2,
    "not_provided|Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype": 6,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|DMD-related_disorder|not_specified|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided": 3,
    "Progressive_muscular_dystrophy": 2,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Dilated_cardiomyopathy_3B|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|not_provided": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 2,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype": 2,
    "not_provided|Duchenne_muscular_dystrophy|not_specified|DMD-related_disorder|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "not_specified|Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy": 3,
    "Duchenne_muscular_dystrophy|not_provided|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency": 1,
    "Cardiovascular_phenotype|not_specified|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided": 3,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|not_provided": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 1,
    "not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Duchenne_muscular_dystrophy|not_provided": 1,
    "DMD-related_disorder|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_provided": 2,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|not_provided": 3,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_provided|DMD-related_disorder": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|not_provided|Progressive_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 2,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified": 2,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "not_specified|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Duchenne_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_specified|Primary_dilated_cardiomyopathy|DMD-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided": 4,
    "Duchenne_and_Becker_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided": 1,
    "not_specified|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy": 2,
    "Cardiovascular_phenotype|Dystrophin_deficiency|not_specified|not_provided|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Progressive_muscular_dystrophy": 1,
    "not_provided|Duchenne_muscular_dystrophy|See_cases": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 5,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|not_specified|DMD-related_disorder": 1,
    "not_provided|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|not_provided": 1,
    "not_provided|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified": 1,
    "not_provided|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Long_QT_syndrome|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "DMD-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|DMD-related_disorder|not_specified|not_provided|Duchenne_muscular_dystrophy": 1,
    "not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|not_provided": 8,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dystrophin_deficiency": 2,
    "Duchenne_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 6,
    "not_specified|Dystrophin_deficiency|Duchenne_muscular_dystrophy": 1,
    "DMD-related_disorder|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiovascular_phenotype": 4,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B": 2,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|DMD-related_disorder|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|not_provided|Dilated_cardiomyopathy_3B": 5,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystonia|_early-onset|_and/or_spastic_paraplegia|not_provided": 1,
    "DMD-related_disorder|Cardiovascular_phenotype|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|Dilated_cardiomyopathy_3B|not_provided": 1,
    "EMG:_myopathic_abnormalities|Shoulder_girdle_muscle_weakness|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|DMD-related_disorder|not_provided|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Proximal_muscle_weakness|Highly_elevated_creatine_kinase": 1,
    "Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 2,
    "DMD-related_disorder|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "Muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "not_provided|Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 2,
    "not_provided|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 4,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 3,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B": 2,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_specified|DMD-related_disorder": 1,
    "Duchenne_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|not_specified": 2,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 3,
    "Primary_dilated_cardiomyopathy|Calf_muscle_hypertrophy|Progressive_muscle_weakness|Abnormal_muscle_fiber_dystrophin_expression|Duchenne_muscular_dystrophy": 1,
    "DMD-related_disorder|Cardiovascular_phenotype": 2,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|DMD-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "not_provided|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "DMD-related_disorder|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|not_provided|Duchenne_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 2,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|not_specified|Dilated_cardiomyopathy_3B": 2,
    "not_provided|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Primary_dilated_cardiomyopathy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_specified|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy": 1,
    "Dystrophin_deficiency|not_provided|Duchenne_muscular_dystrophy|not_specified": 1,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_specified": 1,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "not_provided|not_specified|Duchenne_muscular_dystrophy|Dystrophin_deficiency": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|not_provided": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "not_specified|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified": 2,
    "Muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_specified": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Inborn_genetic_diseases": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified": 2,
    "Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_specified|DMD-related_disorder|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Primary_familial_dilated_cardiomyopathy|Duchenne_muscular_dystrophy": 1,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B": 2,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided|Dilated_cardiomyopathy_3B": 1,
    "not_provided|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided|not_specified": 2,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified": 2,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|not_provided|Dystrophin_deficiency": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|not_provided": 3,
    "not_specified|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided|Cardiovascular_phenotype": 1,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_specified": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency": 2,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype": 2,
    "not_provided|not_specified|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 1,
    "Duchenne_muscular_dystrophy|Duchenne_and_Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_provided|not_specified": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_specified|not_provided": 2,
    "Duchenne_muscular_dystrophy|Elevated_circulating_creatine_kinase_concentration": 1,
    "Cardiovascular_phenotype|not_provided|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 1,
    "not_specified|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_specified|DMD-related_disorder|Duchenne_muscular_dystrophy": 1,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy": 1,
    "DMD-related_disorder|not_specified|not_provided|Duchenne_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|not_specified|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|not_provided": 1,
    "DMD-related_disorder|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy": 3,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 4,
    "Duchenne_muscular_dystrophy|Abnormality_of_the_musculature": 3,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 2,
    "not_provided|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype": 2,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_specified|not_provided|Intellectual_disability": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|not_provided": 2,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|not_provided": 1,
    "not_provided|not_specified|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|not_specified|not_provided": 1,
    "Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 2,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype": 1,
    "Dilated_cardiomyopathy_3B|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided|Cardiovascular_phenotype": 1,
    "not_specified|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Highly_elevated_creatine_kinase": 1,
    "DMD-related_disorder|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|DMD-related_disorder": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "not_specified|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Hereditary_skeletal_muscle_disorder|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "not_provided|Duchenne_muscular_dystrophy|Abnormality_of_the_musculature": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|DMD-related_disorder|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|DMD-related_disorder|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 2,
    "Dystrophin_deficiency|not_specified": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_provided": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided|not_specified": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|not_provided|Dilated_cardiomyopathy_3B": 2,
    "not_specified|not_provided|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified": 1,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Duchenne_muscular_dystrophy|Intellectual_disability": 1,
    "not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided": 1,
    "Abnormality_of_the_musculature|not_provided": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|not_provided": 1,
    "Progressive_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B": 2,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 2,
    "Duchenne_muscular_dystrophy|Duchenne_and_Becker_muscular_dystrophy": 1,
    "Progressive_muscular_dystrophy|not_provided|Duchenne_muscular_dystrophy": 1,
    "not_provided|DMD-related_disorder": 1,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_specified": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_specified|not_provided": 2,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "not_provided|DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|Familial_restrictive_cardiomyopathy|Cardiovascular_phenotype": 1,
    "DMD-related_disorder|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|not_provided|not_specified": 1,
    "Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy|Primary_dilated_cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified|not_provided": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|DMD-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Progressive_muscular_dystrophy": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified": 2,
    "DMD-related_disorder|not_provided|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "DMD-related_disorder|Cardiovascular_phenotype|Duchenne_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|Abnormality_of_the_musculature|not_provided": 2,
    "Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|not_provided|Becker_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|DMD-related_disorder|not_specified|not_provided": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|not_specified|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|not_specified": 2,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|DMD-related_disorder|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|See_cases": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|Cardiovascular_phenotype|DMD-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Muscular_dystrophy|Exertional_myalgia|_muscle_stiffness_and_myoglobinuria|not_specified|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|Dystrophin_deficiency": 1,
    "not_specified|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_specified": 1,
    "Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|not_provided|Cardiovascular_phenotype|not_specified|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Duchenne_muscular_dystrophy|Muscle_spasm|EMG_abnormality|EMG:_myopathic_abnormalities|Calf_muscle_hypertrophy|Motor_delay|Muscle_weakness|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Conduction_disorder_of_the_heart|not_provided": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|DMD-related_disorder|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|not_provided|Cardiovascular_phenotype|not_specified": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided|Cardiovascular_phenotype": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency": 1,
    "Cardiovascular_phenotype|not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|DMD-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B|Mitochondrial_disease|Restrictive_cardiomyopathy|Intellectual_disability": 1,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|not_provided|Duchenne_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|Dystrophin_deficiency|Cardiomyopathy": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Long_QT_syndrome|Brugada_syndrome|not_specified|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Intermediate_muscular_dystrophy": 1,
    "not_provided|Becker_muscular_dystrophy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Duchenne_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_3B|not_provided|Primary_dilated_cardiomyopathy|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|DMD-related_disorder": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|not_provided|not_specified": 1,
    "Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|DMD-related_disorder": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided": 1,
    "Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B": 1,
    "DMD-related_disorder|not_provided|Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Becker_muscular_dystrophy|not_specified|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided": 1,
    "Cardiomyopathy|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided": 1,
    "Dystrophin_deficiency|not_specified|not_provided": 1,
    "Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|not_provided|not_specified": 1,
    "Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 1,
    "Dilated_cardiomyopathy_3B|not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "not_provided|Duchenne_muscular_dystrophy|Cardiovascular_phenotype|DMD-related_disorder": 1,
    "DMD-related_disorder|not_provided|Duchenne_muscular_dystrophy|not_specified|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|Arrhythmogenic_right_ventricular_cardiomyopathy|not_provided|Dystrophin_deficiency|Cardiomyopathy|Becker_muscular_dystrophy": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency": 1,
    "DMD-related_disorder|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Duchenne_muscular_dystrophy|DMD-related_disorder|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Duchenne_muscular_dystrophy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Duchenne_muscular_dystrophy|Dystrophin_deficiency": 1,
    "Duchenne_muscular_dystrophy|not_provided|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Duchenne_muscular_dystrophy|Elevated_circulating_creatine_kinase_concentration": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Dystrophin_deficiency|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy|not_provided": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_specified|not_provided|Arrhythmogenic_right_ventricular_cardiomyopathy": 1,
    "not_specified|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided": 1,
    "not_provided|Dilated_cardiomyopathy_3B|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy": 1,
    "Hypertrophic_cardiomyopathy|Intellectual_disability|Duchenne_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency|Becker_muscular_dystrophy": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|Dilated_cardiomyopathy_3B": 1,
    "Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_specified|DMD-related_disorder|Dystrophin_deficiency|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_specified": 1,
    "Cardiovascular_phenotype|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|not_specified|not_provided": 1,
    "not_provided|Duchenne_muscular_dystrophy|Cardiomyopathy|Becker_muscular_dystrophy|Dystrophin_deficiency": 1,
    "Dilated_cardiomyopathy_3B|Short_stature|Myopathy|EMG:_myopathic_abnormalities|Exercise-induced_muscle_cramps|Exercise-induced_myalgia|Decreased_body_weight|Exercise-induced_muscle_stiffness|Exercise-induced_muscle_fatigue|Exercise-induced_rhabdomyolysis": 1,
    "Duchenne_muscular_dystrophy|Cardiovascular_phenotype|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 1,
    "Intermediate_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|Dilated_cardiomyopathy_3B|not_provided": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided|not_specified": 1,
    "DMD-related_disorder|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Cardiovascular_phenotype|not_provided": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Dilated_cardiomyopathy_3B|not_provided|not_specified": 1,
    "DMD-related_disorder|not_provided|Duchenne_muscular_dystrophy": 1,
    "not_specified|Becker_muscular_dystrophy|Duchenne_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|not_provided": 1,
    "Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Dystrophin_deficiency|not_specified": 2,
    "not_provided|Becker_muscular_dystrophy|Becker_muscular_dystrophy|_atypical": 1,
    "Achondroplasia|Color_vision_defect": 1,
    "not_provided|Duchenne_muscular_dystrophy|Color_vision_defect": 1,
    "Elevated_circulating_creatine_kinase_concentration|Atrial_septal_defect|Dilated_cardiomyopathy_3B": 1,
    "DMD-related_disorder|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Duchenne_muscular_dystrophy|Dystrophin_deficiency|Becker_muscular_dystrophy|Cardiomyopathy|not_specified": 1,
    "not_provided|Becker_muscular_dystrophy|_Cardiomyopathy|_Duchenne_muscular_dystrophy|_Dystrophin_deficiency": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_provided|DMD-related_disorder|not_specified": 1,
    "Cardiovascular_phenotype|Dystrophin_deficiency|Cardiomyopathy|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided": 1,
    "Becker_muscular_dystrophy|Cardiomyopathy|Duchenne_muscular_dystrophy|Dystrophin_deficiency|not_specified|DMD-related_disorder|not_provided": 1,
    "Cardiovascular_phenotype|Duchenne_muscular_dystrophy|Dilated_cardiomyopathy_3B|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin|Becker_muscular_dystrophy": 1,
    "Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Dilated_cardiomyopathy_3B": 1,
    "not_provided|Becker_muscular_dystrophy|Cardiomyopathy|Dystrophin_deficiency|Duchenne_muscular_dystrophy": 1,
    "Dystrophin_deficiency|Dilated_cardiomyopathy_3B|Duchenne_muscular_dystrophy|Becker_muscular_dystrophy|not_provided|Neuromuscular_disease_caused_by_qualitative_or_quantitative_defects_of_dystrophin": 1,
    "Duchenne_muscular_dystrophy|not_provided|Dilated_cardiomyopathy_3B|Becker_muscular_dystrophy": 1,
    "Dilated_cardiomyopathy_3B|not_provided|not_specified": 1,
    "FAM47A-related_disorder": 7,
    "not_provided|FAM47A-related_disorder": 2,
    "Attention_deficit_hyperactivity_disorder|Hypotonia|Hypoplasia_of_the_corpus_callosum|Cerebellar_atrophy|Global_developmental_delay|Dandy-Walker_syndrome": 2,
    "FAM47B-related_disorder": 12,
    "CFAP47-related_disorder": 9,
    "Spermatogenic_failure|_X-linked|_3": 5,
    "McLeod_neuroacanthocytosis_syndrome|not_provided": 2,
    "McLeod_neuroacanthocytosis_syndrome": 20,
    "XK-related_disorder": 1,
    "XK-related_disorder|not_provided": 1,
    "not_provided|McLeod_neuroacanthocytosis_syndrome": 2,
    "Inborn_genetic_diseases|McLeod_neuroacanthocytosis_syndrome": 1,
    "Granulomatous_disease|_chronic|_X-linked": 489,
    "not_provided|Granulomatous_disease|_chronic|_X-linked": 23,
    "Granulomatous_disease|_chronic|_X-linked|Chronic_granulomatous_disease": 16,
    "Inborn_genetic_diseases|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked": 17,
    "Granulomatous_disease|_chronic|_X-linked|not_specified|Chronic_granulomatous_disease": 1,
    "Chronic_granulomatous_disease|not_specified|Granulomatous_disease|_chronic|_X-linked": 1,
    "Granulomatous_disease|_chronic|_X-linked|not_specified": 5,
    "Granulomatous_disease|_chronic|_X-linked|not_provided": 22,
    "Chronic_granulomatous_disease|CYBB-related_disorder|Granulomatous_disease|_chronic|_X-linked": 1,
    "Granulomatous_disease|_chronic|_X-linked|not_provided|Chronic_granulomatous_disease": 1,
    "Granulomatous_disease|_chronic|_X-linked|CYBB-related_disorder|not_provided": 1,
    "Granulomatous_disease|_chronic|_X-linked|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Granulomatous_disease|_chronic|_X-linked": 3,
    "not_provided|Granulomatous_disease|_chronic|_X-linked|Granulomatous_disease|_chronic|_X-linked|_variant": 3,
    "CYBB-related_disorder|Granulomatous_disease|_chronic|_X-linked": 2,
    "not_specified|Chronic_granulomatous_disease": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked|CYBB-related_disorder": 1,
    "Granulomatous_disease|_chronic|_X-linked|_variant|not_provided|Granulomatous_disease|_chronic|_X-linked": 1,
    "not_provided|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked": 3,
    "not_specified|Granulomatous_disease|_chronic|_X-linked|Chronic_granulomatous_disease": 1,
    "Granulomatous_disease|_chronic|_X-linked|Inborn_genetic_diseases": 1,
    "Chronic_granulomatous_disease|not_provided|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency": 2,
    "not_specified|Granulomatous_disease|_chronic|_X-linked": 5,
    "Granulomatous_disease|_chronic|_X-linked|not_specified|CYBB-related_disorder|not_provided": 1,
    "Granulomatous_disease|_chronic|_X-linked|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency|Chronic_granulomatous_disease|not_provided": 1,
    "X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency|Granulomatous_disease|_chronic|_X-linked": 2,
    "CYBB-related_disorder": 2,
    "CYBB-related_disorder|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked": 1,
    "Granulomatous_disease|_chronic|_X-linked|Inborn_genetic_diseases|Chronic_granulomatous_disease": 1,
    "not_provided|Granulomatous_disease|_chronic|_X-linked|_variant": 3,
    "Granulomatous_disease|_chronic|_X-linked|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency": 1,
    "Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked|not_provided": 1,
    "not_specified|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency|Granulomatous_disease|_chronic|_X-linked|not_provided": 1,
    "Granulomatous_disease|_chronic|_X-linked|Primary_ciliary_dyskinesia|Recurrent_bronchitis|Dynein_arm_defect_of_respiratory_motile_cilia": 1,
    "Chronic_granulomatous_disease|not_provided": 1,
    "Inborn_genetic_diseases|CYBB-related_disorder": 1,
    "Granulomatous_disease|_chronic|_X-linked|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency|Chronic_granulomatous_disease": 1,
    "Granulomatous_disease|_chronic|_X-linked|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Granulomatous_disease|_chronic|_X-linked|Chronic_granulomatous_disease": 1,
    "Granulomatous_disease|_chronic|_X-linked|not_specified|X-linked_Mendelian_susceptibility_to_mycobacterial_diseases_due_to_CYBB_deficiency|not_provided|Chronic_granulomatous_disease|CYBB-related_disorder": 1,
    "not_specified|Chronic_granulomatous_disease|Granulomatous_disease|_chronic|_X-linked": 1,
    "CYBB-related_disorder|Granulomatous_disease|_chronic|_X-linked|not_specified|not_provided": 1,
    "Granulomatous_disease|_chronic|_X-linked|Inborn_genetic_diseases|not_specified|CYBB-related_disorder": 1,
    "not_specified|SYTL5-related_disorder": 1,
    "SYTL5-related_disorder": 3,
    "SYTL5-related_disorder|not_specified": 1,
    "RPGR-related_disorder": 8,
    "Primary_ciliary_dyskinesia|RPGR-related_disorder": 7,
    "Primary_ciliary_dyskinesia|Retinal_dystrophy": 16,
    "not_specified|not_provided|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|X-linked_cone-rod_dystrophy_1": 1,
    "Macular_degeneration|_X-linked_atrophic|not_specified|not_provided|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1": 1,
    "not_provided|RPGR-related_retinopathy": 18,
    "RPGR-related_retinopathy|not_provided": 14,
    "RPGR-related_retinopathy": 39,
    "Retinitis_pigmentosa_3|RPGR-related_retinopathy": 5,
    "Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 9,
    "RPGR-related_retinopathy|Primary_ciliary_dyskinesia|not_provided|Retinal_dystrophy|not_specified": 1,
    "Macular_dystrophy|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 1,
    "RPGR-related_retinopathy|not_provided|Primary_ciliary_dyskinesia": 8,
    "Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia": 8,
    "Retinitis_pigmentosa|RPGR-related_retinopathy|Retinal_dystrophy|not_provided": 1,
    "RPGR-related_retinopathy|Primary_ciliary_dyskinesia": 9,
    "Retinal_dystrophy|X-linked_cone-rod_dystrophy_1": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 1,
    "Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "not_provided|Retinitis_pigmentosa_3|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|X-linked_cone-rod_dystrophy_1": 1,
    "not_provided|Retinal_dystrophy|not_specified|Primary_ciliary_dyskinesia": 1,
    "not_provided|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3": 2,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1": 1,
    "RPGR-related_retinopathy|not_specified|Primary_ciliary_dyskinesia|not_provided": 3,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_3": 78,
    "X-linked_cone-rod_dystrophy_1": 6,
    "not_provided|RPGR-related_disorder|Retinal_dystrophy|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 1,
    "Primary_ciliary_dyskinesia|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1|Cone-rod_dystrophy|not_provided|Retinal_dystrophy": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 7,
    "Primary_ciliary_dyskinesia|not_provided|Retinal_dystrophy": 5,
    "Primary_ciliary_dyskinesia|not_provided|RPGR-related_retinopathy": 5,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinal_dystrophy": 6,
    "Retinal_dystrophy|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|RPGR-related_retinopathy|Retinitis_pigmentosa": 1,
    "RPGR-related_retinopathy|Cone_dystrophy_1|_X-linked|RPGR-related_disorder|Retinal_dystrophy|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1|Cone_dystrophy": 1,
    "RPGR-related_retinopathy|RPGR-related_disorder|Retinal_dystrophy|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1|Cone_dystrophy": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa|RPGR-related_retinopathy|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1": 1,
    "Retinitis_pigmentosa_3|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 3,
    "Retinitis_pigmentosa_3|RPGR-related_retinopathy|Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1": 2,
    "Retinitis_pigmentosa|Primary_ciliary_dyskinesia": 6,
    "RPGR-related_retinopathy|Primary_ciliary_dyskinesia|not_provided": 2,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|not_provided": 4,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|not_provided|Retinitis_pigmentosa|RPGR-related_retinopathy": 1,
    "not_provided|RPGR-related_disorder|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_3|Retinal_dystrophy": 16,
    "not_provided|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|Retinitis_pigmentosa_3": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 6,
    "not_provided|Retinitis_pigmentosa_3|Retinitis_pigmentosa|Primary_ciliary_dyskinesia": 1,
    "RPGR-related_retinopathy|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_3|Retinal_dystrophy|not_provided": 1,
    "Macular_degeneration|_X-linked_atrophic|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|RPGR-related_retinopathy|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|not_provided": 3,
    "Retinal_dystrophy|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 4,
    "Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 1,
    "RPGR-related_retinopathy|X-linked_cone-rod_dystrophy_1": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|Retinal_dystrophy|not_provided": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinal_dystrophy|not_provided": 2,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_3": 2,
    "Retinitis_pigmentosa_3|Retinal_dystrophy|Primary_ciliary_dyskinesia": 3,
    "RPGR-related_disorder|Primary_ciliary_dyskinesia": 2,
    "not_provided|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|Retinal_dystrophy": 1,
    "X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|Primary_ciliary_dyskinesia|not_provided": 1,
    "Retinitis_pigmentosa_3|RPGR-related_retinopathy|Retinal_dystrophy|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa|Retinitis_pigmentosa_3|RPGR-related_retinopathy": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa|Retinitis_pigmentosa_3|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_3": 5,
    "not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinal_dystrophy": 3,
    "Primary_ciliary_dyskinesia|RPGR-related_disorder|Retinitis_pigmentosa_3": 1,
    "not_provided|RPGR-related_retinopathy|Retinal_dystrophy": 2,
    "not_provided|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 6,
    "not_provided|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|not_provided|Retinal_dystrophy": 1,
    "not_provided|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|RPGR-related_retinopathy|not_provided": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 1,
    "RPGR-related_retinopathy|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 3,
    "not_specified|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|not_provided|X-linked_cone-rod_dystrophy_1": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|Primary_ciliary_dyskinesia": 1,
    "not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_3|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|Retinal_dystrophy": 1,
    "X-linked_cone-rod_dystrophy|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|Retinitis_pigmentosa|RPGR-related_disorder": 1,
    "Retinitis_pigmentosa_3|RPGR-related_retinopathy|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_3|RPGR-related_retinopathy": 2,
    "RPGR-related_retinopathy|not_provided|Retinitis_pigmentosa_3": 1,
    "not_provided|Retinal_dystrophy|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 2,
    "Primary_ciliary_dyskinesia|X-linked_cone-rod_dystrophy_1": 4,
    "not_provided|Retinitis_pigmentosa|RPGR-related_retinopathy": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Primary_ciliary_dyskinesia|Retinal_dystrophy|not_provided": 2,
    "RPGR-related_retinopathy|Retinitis_pigmentosa_3": 3,
    "X-linked_cone-rod_dystrophy_1|not_provided|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_3|Retinal_dystrophy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_3|Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa|RPGR-related_retinopathy": 2,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa|Retinitis_pigmentosa_3": 1,
    "Retinal_dystrophy|Primary_ciliary_dyskinesia": 8,
    "RPGR-related_disorder|Retinal_dystrophy|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia": 1,
    "not_provided|RPGR-related_retinopathy|Primary_ciliary_dyskinesia": 3,
    "RPGR-related_retinopathy|Inborn_genetic_diseases|Retinal_dystrophy|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_3|Retinal_dystrophy|Primary_ciliary_dyskinesia|Retinitis_pigmentosa": 1,
    "not_provided|Primary_ciliary_dyskinesia|Retinal_dystrophy": 4,
    "Primary_ciliary_dyskinesia|X-linked_cone-rod_dystrophy": 3,
    "Retinitis_pigmentosa_3|not_provided|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "not_specified|Retinal_dystrophy|RPGR-related_retinopathy|not_provided|Primary_ciliary_dyskinesia": 1,
    "not_provided|Retinitis_pigmentosa_3|RPGR-related_retinopathy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_3|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_3|Retinal_dystrophy|not_provided": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_3|RPGR-related_retinopathy": 1,
    "Retinal_dystrophy|RPGR-related_retinopathy|Retinitis_pigmentosa|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 1,
    "RPGR-related_retinopathy|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|Retinal_dystrophy|not_provided": 1,
    "not_provided|Retinitis_pigmentosa_3": 8,
    "not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinal_dystrophy|RPGR-related_retinopathy": 1,
    "Retinal_dystrophy|X-linked_cone-rod_dystrophy_1|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|RPGR-related_disorder|RPGR-related_retinopathy|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Primary_ciliary_dyskinesia|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|not_provided": 1,
    "not_provided|not_specified|Retinal_dystrophy|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|not_provided|RPGR-related_retinopathy": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinitis_pigmentosa": 1,
    "X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|not_provided|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 1,
    "Primary_ciliary_dyskinesia|Retinal_dystrophy|RPGR-related_retinopathy": 1,
    "Retinitis_pigmentosa|RPGR-related_retinopathy|not_provided|Retinitis_pigmentosa_3": 1,
    "Primary_ciliary_dyskinesia|not_provided|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|RPGR-related_retinopathy": 1,
    "Retinitis_pigmentosa_3|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|X-linked_cone-rod_dystrophy_1": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy": 10,
    "Primary_ciliary_dyskinesia|Retinal_dystrophy|not_provided|RPGR-related_retinopathy": 1,
    "X-linked_cone-rod_dystrophy_1|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|not_provided|Primary_ciliary_dyskinesia": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_specified|Primary_ciliary_dyskinesia|not_provided": 2,
    "not_provided|Primary_ciliary_dyskinesia|not_specified|RPGR-related_disorder": 1,
    "RPGR-related_retinopathy|not_specified|not_provided|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 1,
    "Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia|X-linked_cone-rod_dystrophy_1": 2,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa": 2,
    "Retinal_dystrophy|RPGR-related_retinopathy|Primary_ciliary_dyskinesia|not_provided": 1,
    "Primary_ciliary_dyskinesia|RPGR-related_retinopathy|Retinal_dystrophy": 2,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|RPGR-related_retinopathy": 1,
    "Macular_degeneration|_X-linked_atrophic": 1,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|RPGR-related_disorder": 1,
    "RPGR-related_retinopathy|Primary_ciliary_dyskinesia|RPGR-related_disorder": 1,
    "Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_provided|not_specified|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|not_provided": 1,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|RPGR-related_retinopathy|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1": 1,
    "Primary_ciliary_dyskinesia|not_specified|not_provided|RPGR-related_retinopathy": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_specified|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_specified|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|Primary_ciliary_dyskinesia|not_provided|Retinitis_pigmentosa_3": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa|Retinal_dystrophy|RPGR-related_retinopathy|not_provided": 1,
    "X-linked_cone-rod_dystrophy_1|Macular_degeneration|_X-linked_atrophic|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|not_provided|RPGR-related_retinopathy|Primary_ciliary_dyskinesia": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa|Retinal_dystrophy|not_provided": 1,
    "X-linked_cone-rod_dystrophy_1|See_cases": 1,
    "not_provided|not_specified|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|X-linked_cone-rod_dystrophy_1|Macular_degeneration|_X-linked_atrophic": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|Primary_ciliary_dyskinesia|not_provided": 1,
    "RPGR-related_retinopathy|not_provided|Primary_ciliary_dyskinesia|Retinal_dystrophy": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia": 2,
    "not_specified|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 1,
    "RPGR-related_retinopathy|not_provided|Primary_ciliary_dyskinesia|not_specified": 1,
    "Primary_ciliary_dyskinesia|Retinal_dystrophy|RPGR-related_disorder": 1,
    "Primary_ciliary_dyskinesia|Retinal_dystrophy|not_provided": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_provided": 1,
    "Primary_ciliary_dyskinesia|RPGR-related_retinopathy|RPGR-related_disorder": 1,
    "X-linked_cone-rod_dystrophy|RPGR-related_retinopathy": 2,
    "RPGR-related_retinopathy|Retinitis_pigmentosa": 1,
    "Retinitis_pigmentosa_6": 1,
    "RPGR-related_retinopathy|RPGR-related_disorder|not_specified|not_provided|Primary_ciliary_dyskinesia|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|Primary_ciliary_dyskinesia|RPGR-related_retinopathy": 2,
    "RPGR-related_retinopathy|Primary_ciliary_dyskinesia|not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_3": 1,
    "RETINITIS_PIGMENTOSA|_SINORESPIRATORY_INFECTIONS|_AND_DEAFNESS": 1,
    "Primary_ciliary_dyskinesia|RPGR-related_retinopathy|not_provided": 1,
    "Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness": 1,
    "Retinitis_pigmentosa_3|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|not_provided": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3|Retinitis_pigmentosa|RPGR-related_retinopathy": 1,
    "not_specified|Primary_ciliary_dyskinesia|RPGR-related_retinopathy|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa_3|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Macular_degeneration|_X-linked_atrophic|not_provided": 1,
    "RPGR-related_retinopathy|RETINITIS_PIGMENTOSA|_SINORESPIRATORY_INFECTIONS|_AND_DEAFNESS|not_provided": 1,
    "Retinitis_pigmentosa|RPGR-related_retinopathy|X-linked_cone-rod_dystrophy_1": 1,
    "Retinitis_pigmentosa|Retinal_dystrophy|RPGR-related_retinopathy": 1,
    "RPGR-related_retinopathy|Retinal_dystrophy|not_provided|Primary_ciliary_dyskinesia|X-linked_cone-rod_dystrophy_1": 1,
    "RPGR-related_retinopathy|not_provided|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness": 1,
    "RPGR-related_disorder|RPGR-related_retinopathy|Primary_ciliary_dyskinesia": 1,
    "Retinitis_pigmentosa_3|not_provided|RPGR-related_retinopathy": 1,
    "Primary_ciliary_dyskinesia|Retinitis_pigmentosa|RPGR-related_retinopathy": 1,
    "Retinitis_pigmentosa_3|not_provided": 3,
    "not_provided|Retinal_dystrophy|Retinitis_pigmentosa|Primary_ciliary_dyskinesia": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_3|not_provided": 1,
    "RPGR-related_retinopathy|not_specified|X-linked_cone-rod_dystrophy_1|Retinitis_pigmentosa|_X-linked|_and_sinorespiratory_infections|_with_or_without_deafness|Retinitis_pigmentosa_3|Macular_degeneration|_X-linked_atrophic|not_provided|Primary_ciliary_dyskinesia": 1,
    "RPGR-related_retinopathy|RPGR-related_disorder|Retinal_dystrophy|Primary_ciliary_dyskinesia|not_provided|Retinitis_pigmentosa_3": 1,
    "Cone-rod_dystrophy|RPGR-related_disorder": 1,
    "RPGR-related_retinopathy|not_provided|Retinal_dystrophy|Primary_ciliary_dyskinesia|Retinitis_pigmentosa_3": 1,
    "not_specified|not_provided|Primary_ciliary_dyskinesia|RPGR-related_disorder": 1,
    "OTC-related_disorder|not_specified": 1,
    "OTC-related_disorder": 3,
    "not_provided|Ornithine_carbamoyltransferase_deficiency|OTC-related_disorder|not_specified": 1,
    "Ornithine_carbamoyltransferase_deficiency|not_specified": 6,
    "Ornithine_carbamoyltransferase_deficiency": 443,
    "not_provided|Ornithine_carbamoyltransferase_deficiency": 69,
    "Ornithine_carbamoyltransferase_deficiency|not_provided": 86,
    "OTC-related_disorder|Ornithine_carbamoyltransferase_deficiency": 1,
    "Inborn_genetic_diseases|Ornithine_carbamoyltransferase_deficiency": 5,
    "Inborn_genetic_diseases|not_provided|Ornithine_carbamoyltransferase_deficiency": 4,
    "OTC-related_disorder|Inborn_genetic_diseases|Ornithine_carbamoyltransferase_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|Ornithine_carbamoyltransferase_deficiency|not_provided": 1,
    "Ornithine_carbamoyltransferase_deficiency|Inborn_genetic_diseases": 5,
    "not_specified|Ornithine_carbamoyltransferase_deficiency": 8,
    "OTC-related_disorder|not_provided|not_specified|Ornithine_carbamoyltransferase_deficiency": 1,
    "not_provided|not_specified|Ornithine_carbamoyltransferase_deficiency": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Ornithine_carbamoyltransferase_deficiency|ORNITHINE_TRANSCARBAMYLASE_POLYMORPHISM": 1,
    "Ornithine_carbamoyltransferase_deficiency|Inborn_genetic_diseases|not_specified|not_provided|OTC-related_disorder": 1,
    "Ornithine_carbamoyltransferase_deficiency|not_specified|not_provided": 3,
    "Ornithine_carbamoyltransferase_deficiency|OTC-related_disorder": 5,
    "Inborn_genetic_diseases|Ornithine_carbamoyltransferase_deficiency|not_specified": 1,
    "Ornithine_carbamoyltransferase_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Ornithine_carbamoyltransferase_deficiency|OTC-related_disorder|not_specified|not_provided": 1,
    "Ornithine_carbamoyltransferase_deficiency|not_provided|not_specified": 1,
    "not_specified|not_provided|Ornithine_carbamoyltransferase_deficiency|Inborn_genetic_diseases": 2,
    "Hyperammonemia|not_specified|not_provided|Ornithine_carbamoyltransferase_deficiency": 1,
    "not_specified|not_provided|Ornithine_carbamoyltransferase_deficiency": 2,
    "not_provided|Ornithine_carbamoyltransferase_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|OTC-related_disorder|Ornithine_carbamoyltransferase_deficiency": 1,
    "not_provided|Ornithine_carbamoyltransferase_deficiency|Hyperammonemia|Abnormal_circulating_ornithine_concentration|Protein_avoidance": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Ornithine_carbamoyltransferase_deficiency": 1,
    "Ornithine_carbamoyltransferase_deficiency|OTC-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Ornithine_carbamoyltransferase_deficiency|not_provided": 2,
    "Ornithine_carbamoyltransferase_deficiency|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|OTC-related_disorder": 1,
    "OTC-related_disorder|not_provided": 1,
    "Global_developmental_delay|Hyperammonemia|Ornithine_carbamoyltransferase_deficiency": 1,
    "not_specified|Intellectual_disability|_X-linked_58": 1,
    "Intellectual_disability|_X-linked_58|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked_58": 6,
    "TSPAN7-related_disorder|not_specified": 1,
    "TSPAN7-related_disorder|not_provided": 1,
    "not_specified|TSPAN7-related_disorder": 1,
    "not_provided|History_of_neurodevelopmental_disorder|Intellectual_disability|_X-linked_58": 1,
    "TSPAN7-related_disorder|not_provided|not_specified": 1,
    "not_specified|Oculofaciocardiodental_syndrome": 11,
    "not_provided|Oculofaciocardiodental_syndrome": 26,
    "Oculofaciocardiodental_syndrome": 302,
    "Inborn_genetic_diseases|Oculofaciocardiodental_syndrome": 12,
    "BCOR-related_disorder": 18,
    "Inborn_genetic_diseases|BCOR-related_disorder|Oculofaciocardiodental_syndrome": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Oculofaciocardiodental_syndrome": 3,
    "Inborn_genetic_diseases|Oculofaciocardiodental_syndrome|not_provided": 1,
    "Oculofaciocardiodental_syndrome|Inborn_genetic_diseases": 9,
    "BCOR-related_disorder|Oculofaciocardiodental_syndrome|not_provided": 2,
    "BCOR-related_disorder|Oculofaciocardiodental_syndrome": 10,
    "Oculofaciocardiodental_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Oculofaciocardiodental_syndrome|not_specified": 8,
    "Oculofaciocardiodental_syndrome|not_provided": 15,
    "Oculofaciocardiodental_syndrome|BCOR-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Corpus_callosum|_agenesis_of|Brachycephaly|Microcephaly|Congenital_cerebellar_hypoplasia|Mild_fetal_ventriculomegaly": 1,
    "Microphthalmia|_syndromic_1|Oculofaciocardiodental_syndrome|not_specified": 1,
    "Oculofaciocardiodental_syndrome|BCOR-related_disorder|not_specified|not_provided": 1,
    "not_provided|Oculofaciocardiodental_syndrome|BCOR-related_disorder|not_specified": 1,
    "Oculofaciocardiodental_syndrome|not_specified|Abnormal_brain_morphology": 1,
    "not_provided|Inborn_genetic_diseases|Oculofaciocardiodental_syndrome": 1,
    "Oculofaciocardiodental_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "BCOR-related_disorder|not_provided|Oculofaciocardiodental_syndrome": 3,
    "not_specified|Oculofaciocardiodental_syndrome|BCOR-related_disorder": 2,
    "not_specified|not_provided|Oculofaciocardiodental_syndrome": 4,
    "Inborn_genetic_diseases|not_specified|Oculofaciocardiodental_syndrome|not_provided": 2,
    "Oculofaciocardiodental_syndrome|BCOR-related_disorder": 7,
    "not_provided|Inborn_genetic_diseases|Glioblastoma": 1,
    "not_provided|Oculofaciocardiodental_syndrome|Intellectual_disability": 3,
    "Oculofaciocardiodental_syndrome|not_specified|not_provided|BCOR-related_disorder": 1,
    "not_specified|BCOR-related_disorder|Inborn_genetic_diseases": 1,
    "Oculofaciocardiodental_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|BCOR-related_disorder": 2,
    "Oculofaciocardiodental_syndrome|BCOR-related_disorder|History_of_neurodevelopmental_disorder": 1,
    "Oculofaciocardiodental_syndrome|BCOR-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Oculofaciocardiodental_syndrome|Developmental_cataract": 1,
    "Inborn_genetic_diseases|not_specified|Oculofaciocardiodental_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Oculofaciocardiodental_syndrome": 2,
    "Oculofaciocardiodental_syndrome|not_specified|not_provided": 1,
    "BCOR-related_disorder|not_specified|Oculofaciocardiodental_syndrome": 2,
    "not_provided|Microphthalmia|_syndromic_1|Oculofaciocardiodental_syndrome": 1,
    "not_provided|BCOR-related_disorder|Oculofaciocardiodental_syndrome|Microphthalmia|_syndromic_1": 1,
    "not_specified|Oculofaciocardiodental_syndrome|Intellectual_disability": 1,
    "Microphthalmia|_syndromic_1|Oculofaciocardiodental_syndrome|not_provided": 1,
    "not_specified|Microphthalmia|_syndromic_1|Oculofaciocardiodental_syndrome|BCOR-related_disorder|not_provided": 1,
    "not_specified|History_of_neurodevelopmental_disorder|not_provided|Oculofaciocardiodental_syndrome": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Oculofaciocardiodental_syndrome": 1,
    "Oculofaciocardiodental_syndrome_(OFCD)": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Oculofaciocardiodental_syndrome": 1,
    "not_provided|Developmental_cataract": 1,
    "not_specified|Oculofaciocardiodental_syndrome|Microphthalmia|_syndromic_1": 1,
    "BCOR-related_disorder|History_of_neurodevelopmental_disorder|not_provided": 1,
    "BCOR-related_disorder|not_specified|not_provided|Oculofaciocardiodental_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Oculofaciocardiodental_syndrome|Microphthalmia|_syndromic_1": 1,
    "Inborn_genetic_diseases|BCOR-related_disorder|not_provided": 1,
    "Oculofaciocardiodental_syndrome|Microphthalmia|_syndromic_1|not_specified": 1,
    "History_of_neurodevelopmental_disorder|not_provided|Oculofaciocardiodental_syndrome|not_specified": 1,
    "BCOR-related_disorder|not_provided|not_specified|Oculofaciocardiodental_syndrome": 1,
    "Syndromic_X-linked_intellectual_disability_Hedera_type": 123,
    "not_specified|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "Syndromic_X-linked_intellectual_disability_Hedera_type|Congenital_disorder_of_glycosylation|_type_IIr|X-linked_parkinsonism-spasticity_syndrome|not_specified|ATP6AP2-related_disorder|not_provided": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type": 15,
    "Syndromic_X-linked_intellectual_disability_Hedera_type|not_provided": 3,
    "Syndromic_X-linked_intellectual_disability_Hedera_type|Congenital_disorder_of_glycosylation|_type_IIr": 1,
    "Syndromic_X-linked_intellectual_disability_Hedera_type|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Syndromic_X-linked_intellectual_disability_Hedera_type|History_of_neurodevelopmental_disorder": 1,
    "Congenital_disorder_of_glycosylation|_type_IIr|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type|not_specified": 1,
    "Syndromic_X-linked_intellectual_disability_Hedera_type|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "Syndromic_X-linked_intellectual_disability_Hedera_type|ATP6AP2-related_disorder": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "Congenital_disorder_of_glycosylation|_type_IIr": 2,
    "not_specified|Syndromic_X-linked_intellectual_disability_Hedera_type": 4,
    "not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type|Inborn_genetic_diseases": 1,
    "X-linked_parkinsonism-spasticity_syndrome": 1,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Hedera_type|not_specified": 1,
    "ATP6AP2-related_disorder|Syndromic_X-linked_intellectual_disability_Hedera_type|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type|X-linked_parkinsonism-spasticity_syndrome|Congenital_disorder_of_glycosylation|_type_IIr": 1,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Hedera_type": 3,
    "Congenital_disorder_of_glycosylation|_type_IIr|not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "not_provided|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Hedera_type": 2,
    "not_provided|Inborn_genetic_diseases|not_specified|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "X-linked_parkinsonism-spasticity_syndrome|Syndromic_X-linked_intellectual_disability_Hedera_type|Congenital_disorder_of_glycosylation|_type_IIr|not_provided|Inborn_genetic_diseases": 1,
    "ATP6AP2-related_disorder|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Hedera_type": 1,
    "not_specified|Syndromic_X-linked_intellectual_disability_Hedera_type|Congenital_disorder_of_glycosylation|_type_IIr|X-linked_parkinsonism-spasticity_syndrome": 1,
    "MED14-related_condition": 1,
    "Intellectual_disability|_X-linked_99|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_X-linked_99": 42,
    "Intellectual_disability|_X-linked_99|_syndromic|_female-restricted": 46,
    "USP9X-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Developmental_delay": 1,
    "not_provided|Intellectual_disability|_X-linked_99": 8,
    "USP9X-related_neurodevelopmental_disorder|not_provided|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Intellectual_disability|_X-linked_99": 1,
    "USP9X-related_disorder": 19,
    "Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Intellectual_disability|_X-linked_99": 5,
    "Intellectual_disability|_X-linked_99|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|not_provided": 2,
    "USP9X-related_disorder|not_provided": 8,
    "not_provided|USP9X-related_disorder": 5,
    "Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|not_provided": 3,
    "USP9X-related_neurodevelopmental_disorder": 2,
    "not_provided|USP9X-related_disorder|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted": 1,
    "USP9X-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Intellectual_disability|_X-linked_99|not_provided": 3,
    "not_provided|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Intellectual_disability|_X-linked_99": 2,
    "not_provided|Inborn_genetic_diseases|USP9X-related_disorder": 2,
    "not_provided|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Intellectual_disability|_X-linked_99|not_specified": 1,
    "Intellectual_disability|_X-linked_99|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked_99|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_X-linked_99|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted": 3,
    "Intellectual_disability|_X-linked_101|Intellectual_disability|_X-linked_99|not_provided": 1,
    "Intellectual_disability|_X-linked_99|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Inborn_genetic_diseases|USP9X-related_disorder|not_provided": 1,
    "Intellectual_disability|_X-linked_99|not_provided": 2,
    "not_provided|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted": 1,
    "not_provided|Intellectual_disability|_X-linked_99|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted": 1,
    "Intellectual_disability|_X-linked_99|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted": 1,
    "Hyperpigmentation_of_the_skin": 1,
    "Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|Intellectual_disability|_X-linked_99|not_provided|USP9X-related_intellectual_developmental_disorder": 1,
    "USP9X-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "USP9X-related_disorder|Intellectual_disability|_X-linked_99": 1,
    "USP9X-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_99|Intellectual_disability|_X-linked_99|_syndromic|_female-restricted|not_provided|not_specified|USP9X-related_disorder": 1,
    "DDX3X-related_disorder|not_provided": 4,
    "DDX3X-Related_Neurodevelopmental_Disorder": 1,
    "Intellectual_disability|_X-linked_102|not_provided": 21,
    "DDX3X-related_disorder": 11,
    "not_provided|DDX3X-related_disorder": 2,
    "not_provided|DDX3X-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked_102": 1,
    "not_provided|Intellectual_disability|_X-linked_102": 14,
    "not_provided|Inborn_genetic_diseases|DDX3X-related_disorder": 1,
    "not_provided|DDX3X-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Rare_genetic_intellectual_disability|Intellectual_disability|_X-linked_102|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_102|Inborn_genetic_diseases": 1,
    "DDX3X-related_disorder|Intellectual_disability|_X-linked_102": 1,
    "Neurodevelopmental_disorder|Intellectual_disability|_X-linked_102|not_provided": 1,
    "Intellectual_disability|_X-linked_102|Global_developmental_delay": 1,
    "Intellectual_disability|_X-linked_102|not_provided|DDX3X-related_disorder|Inborn_genetic_diseases|See_cases": 1,
    "not_provided|Intellectual_disability|_X-linked_102|Intellectual_disability": 1,
    "Intellectual_disability|_X-linked_102|not_provided|Inborn_genetic_diseases": 2,
    "DDX3X-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_102|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 1,
    "Intellectual_disability|_X-linked_102|Medulloblastoma": 1,
    "Intellectual_disability|_X-linked_102|See_cases": 1,
    "not_provided|X-linked_syndromic_intellectual_disability": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_102|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_102": 2,
    "Intellectual_disability|_X-linked_102|not_provided|X-linked_intellectual_disability-hypotonia-movement_disorder_syndrome": 1,
    "DDX3X-related_disorder|Intellectual_disability|_X-linked_102|not_provided": 1,
    "Congenital_cerebellar_hypoplasia|not_provided|Intellectual_disability|_X-linked_102|Cerebellar_vermis_hypoplasia": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_102|not_provided": 1,
    "Intellectual_disability|_X-linked_102|Inborn_genetic_diseases|not_provided": 1,
    "DDX3X-related_X-linked_intellectual_disability": 1,
    "X-linked_intellectual_disability-hypotonia-movement_disorder_syndrome|Inborn_genetic_diseases|Intellectual_disability|_X-linked_102|not_provided|Rare_genetic_intellectual_disability": 1,
    "Intellectual_disability|_X-linked_102|Intellectual_disability|See_cases": 1,
    "not_provided|Neurodevelopmental_abnormality|Intellectual_disability|_X-linked_102": 1,
    "DDX3X-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|Intellectual_disability|_X-linked_102|not_provided": 1,
    "not_provided|DDX3X-related_X-linked_intellectual_disability": 1,
    "not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma|Inborn_genetic_diseases|Intellectual_disability|_X-linked_102": 1,
    "Global_developmental_delay|Microcephaly|Delayed_speech_and_language_development": 1,
    "not_provided|DDX3X-related_disorder|Intellectual_disability|_X-linked_102": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_102": 1,
    "Intellectual_disability|not_provided|Intellectual_disability|_X-linked_102": 1,
    "Congenital_stationary_night_blindness_1A": 21,
    "Congenital_stationary_night_blindness_1A|not_provided": 7,
    "not_provided|Congenital_stationary_night_blindness_1A": 9,
    "NYX-related_disorder": 5,
    "Congenital_stationary_night_blindness_1A|NYX-related_disorder|not_provided": 1,
    "not_provided|Congenital_stationary_night_blindness_1A|Inborn_genetic_diseases": 2,
    "Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_1A": 1,
    "NYX-related_disorder|not_provided": 5,
    "not_provided|NYX-related_disorder": 3,
    "Congenital_stationary_night_blindness_1A|Inborn_genetic_diseases": 1,
    "inherited_retinal_disease": 1,
    "Congenital_stationary_night_blindness_1A|not_specified|not_provided": 2,
    "Congenital_stationary_night_blindness|Congenital_stationary_night_blindness_1A": 1,
    "not_provided|not_specified|Congenital_stationary_night_blindness_1A|NYX-related_disorder": 1,
    "not_specified|not_provided|Congenital_stationary_night_blindness_1A": 1,
    "Inborn_genetic_diseases|Congenital_stationary_night_blindness_1A|not_provided": 1,
    "X-linked_congenital_stationary_night_blindness|not_provided": 1,
    "X-linked_congenital_stationary_night_blindness": 1,
    "Intellectual_disability|_CASK-related|_X-linked": 358,
    "not_provided|Intellectual_disability|_CASK-related|_X-linked": 17,
    "FG_syndrome_4": 13,
    "not_provided|Syndromic_X-linked_intellectual_disability_Najm_type|FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases": 6,
    "Syndromic_X-linked_intellectual_disability_Najm_type": 64,
    "Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases|not_provided": 2,
    "CASK-related_disorder": 8,
    "FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked": 4,
    "FG_syndrome_4|Syndromic_X-linked_intellectual_disability_Najm_type": 2,
    "Syndromic_X-linked_intellectual_disability_Najm_type|FG_syndrome_4": 4,
    "FG_syndrome_4|not_specified": 1,
    "not_provided|FG_syndrome_4|Dystonic_disorder|Inability_to_walk|Nystagmus": 1,
    "FG_syndrome": 825,
    "Intellectual_disability|_CASK-related|_X-linked|not_provided": 32,
    "not_provided|not_specified|Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked": 1,
    "not_provided|FG_syndrome_4": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_CASK-related|_X-linked": 8,
    "not_specified|not_provided|Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked|CASK-related_disorder": 1,
    "not_specified|Intellectual_disability|_CASK-related|_X-linked|not_provided": 4,
    "Intellectual_disability|_CASK-related|_X-linked|FG_syndrome_4|Syndromic_X-linked_intellectual_disability_Najm_type|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked": 4,
    "Deficiency_of_butyrylcholinesterase|Syndromic_X-linked_intellectual_disability_Najm_type": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_specified": 6,
    "CASK-related_disorder|not_provided|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Developmental_disorder|FG_syndrome_4|Syndromic_X-linked_intellectual_disability_Najm_type|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases|not_provided": 1,
    "CASK-related_disorder|not_specified|Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked|not_provided": 1,
    "not_provided|Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Najm_type": 1,
    "Global_developmental_delay|Congenital_cerebellar_hypoplasia|Primary_microcephaly|Hypertonia|Nystagmus": 1,
    "FG_syndrome_4|Syndromic_X-linked_intellectual_disability_Najm_type|not_provided": 1,
    "not_provided|Intellectual_disability|_CASK-related|_X-linked|CASK-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_specified|CASK-related_disorder|Inborn_genetic_diseases": 1,
    "Congenital_cerebellar_hypoplasia|Syndromic_X-linked_intellectual_disability_Najm_type": 2,
    "CASK-related_disorder|Intellectual_disability|_CASK-related|_X-linked": 2,
    "Syndromic_X-linked_intellectual_disability_Najm_type|not_provided": 3,
    "CASK-related_disorder|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|_CASK-related|_X-linked": 3,
    "not_specified|Intellectual_disability|_CASK-related|_X-linked": 10,
    "not_provided|Syndromic_X-linked_intellectual_disability_Najm_type": 5,
    "Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked": 7,
    "not_provided|Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability": 1,
    "Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability|_CASK-related|_X-linked": 3,
    "Syndromic_X-linked_intellectual_disability_Najm_type|FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked|not_provided": 1,
    "not_provided|Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked|CASK-related_disorder|not_provided|not_specified": 1,
    "Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability|_CASK-related|_X-linked|not_provided": 1,
    "not_provided|FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked": 1,
    "not_provided|CASK-related_disorder|Intellectual_disability|_CASK-related|_X-linked": 1,
    "not_provided|Intellectual_disability|_CASK-related|_X-linked|CASK-related_disorder": 2,
    "CASK-related_disorder|not_specified|not_provided|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Intellectual_disability|_CASK-related|_X-linked|CASK-related_disorder": 2,
    "not_provided|Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability|_CASK-related|_X-linked": 1,
    "CASK-related_intellectual_disability_and_microcephaly_with_pontine_and_cerebellar_hypoplasia": 1,
    "FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked|not_provided": 2,
    "not_provided|CASK-related_disorder": 1,
    "FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked|not_provided|Abnormality_of_the_nervous_system": 1,
    "CASK-related_disorder|Smith-Magenis_Syndrome-like|Syndromic_X-linked_intellectual_disability_Najm_type|not_provided|Intellectual_disability|_CASK-related|_X-linked": 1,
    "FG_syndrome_4|not_provided": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_provided|Seizure": 1,
    "CASK-related_disorder|Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Najm_type|FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked": 2,
    "not_specified|not_provided|Intellectual_disability|_CASK-related|_X-linked|Inborn_genetic_diseases|CASK-related_disorder": 1,
    "Intellectual_disability|_CASK-related|_X-linked|FG_syndrome_4": 1,
    "CASK-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_provided|not_specified": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_specified|not_provided": 1,
    "not_specified|CASK-related_disorder|not_provided|Inborn_genetic_diseases|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Syndromic_X-linked_intellectual_disability_Najm_type|FG_syndrome_4|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|FG_syndrome_4|Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Intellectual_disability|_CASK-related|_X-linked|FG_syndrome_4|not_specified": 1,
    "Intellectual_disability|_CASK-related|_X-linked|Syndromic_X-linked_intellectual_disability_Najm_type": 1,
    "Intellectual_disability|not_provided|Syndromic_X-linked_intellectual_disability_Najm_type|FG_syndrome_4|Intellectual_disability|_CASK-related|_X-linked": 1,
    "not_specified|not_provided|Intellectual_disability|_CASK-related|_X-linked": 2,
    "Congenital_cerebellar_hypoplasia|not_provided|Syndromic_X-linked_intellectual_disability_Najm_type": 1,
    "Intellectual_disability|_CASK-related|_X-linked|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Congenital_cerebellar_hypoplasia|Syndromic_X-linked_intellectual_disability_Najm_type|Intellectual_disability|_CASK-related|_X-linked": 1,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Najm_type": 1,
    "Brunner_syndrome": 110,
    "Brunner_syndrome|not_provided": 3,
    "not_provided|Brunner_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Brunner_syndrome": 1,
    "Inborn_genetic_diseases|Brunner_syndrome": 6,
    "Brunner_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Brunner_syndrome|not_specified": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Brunner_syndrome": 2,
    "Brunner_syndrome|Inborn_genetic_diseases": 2,
    "Brunner_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Brunner_syndrome|MAOA-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Intellectual_disability|Brunner_syndrome|Inborn_genetic_diseases": 1,
    "Brunner_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Brunner_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "See_cases|Brunner_syndrome|Inborn_genetic_diseases": 1,
    "MAOA-related_disorder": 2,
    "Brunner_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Brunner_syndrome|MAOA-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|MAOA-related_disorder": 1,
    "Brunner_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "History_of_neurodevelopmental_disorder|not_provided": 6,
    "not_provided|NDP-related_disorder": 1,
    "Atrophia_bulborum_hereditaria|not_provided": 4,
    "not_provided|Exudative_vitreoretinopathy_2|_X-linked": 1,
    "Exudative_vitreoretinopathy_2|_X-linked": 4,
    "Atrophia_bulborum_hereditaria|Retinal_dystrophy|not_provided|Exudative_vitreoretinopathy_2|_X-linked": 1,
    "Atrophia_bulborum_hereditaria": 20,
    "Exudative_vitreoretinopathy_2|_X-linked|Atrophia_bulborum_hereditaria": 3,
    "Persistent_hyperplastic_primary_vitreous|High_myopia|Short_lingual_frenulum|Nystagmus": 1,
    "Atrophia_bulborum_hereditaria|not_specified|not_provided|Hearing_impairment": 1,
    "Retinal_dystrophy|Atrophia_bulborum_hereditaria": 1,
    "not_provided|Atrophia_bulborum_hereditaria": 4,
    "Retinal_dystrophy|Atrophia_bulborum_hereditaria|not_provided": 1,
    "Atrophia_bulborum_hereditaria|Exudative_vitreoretinopathy_2|_X-linked|not_provided|Exudative_vitreoretinopathy|_X-linked": 1,
    "NDP-related_disorder": 6,
    "Exudative_retinopathy|Familial_exudative_vitreoretinopathy": 1,
    "X-linked_intellectual_disability|not_provided": 1,
    "Kabuki_syndrome_2": 627,
    "Inborn_genetic_diseases|KDM6A-related_disorder|not_provided|Kabuki_syndrome_2": 1,
    "not_provided|Kabuki_syndrome_2": 53,
    "KDM6A-related_disorder": 24,
    "Kabuki_syndrome_2|not_provided|not_specified": 3,
    "Kabuki_syndrome_2|not_provided": 40,
    "Kabuki_syndrome_2|KDM6A-related_disorder": 10,
    "KDM6A-related_disorder|Intellectual_disability|Kabuki_syndrome_2|not_specified|not_provided": 1,
    "not_provided|Kabuki_syndrome_2|Inborn_genetic_diseases": 4,
    "KDM6A-related_disorder|Kabuki_syndrome_2": 3,
    "Kabuki_syndrome_2|CHARGE_syndrome": 1,
    "Kabuki_syndrome_2|not_specified": 4,
    "Inborn_genetic_diseases|Kabuki_syndrome_2": 10,
    "Kabuki_syndrome_2|Malignant_tumor_of_urinary_bladder|not_provided": 1,
    "not_specified|Kabuki_syndrome_2": 3,
    "Kabuki_syndrome_2|Inborn_genetic_diseases|KDM6A-related_disorder": 1,
    "not_specified|Kabuki_syndrome_2|not_provided": 3,
    "Kabuki_syndrome_1|not_specified|Kabuki_syndrome_2|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Kabuki_syndrome_2": 4,
    "Kabuki_syndrome_2|KDM6A-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Kabuki_syndrome_2": 4,
    "Malignant_tumor_of_urinary_bladder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Kabuki_syndrome_2|not_provided": 1,
    "Kabuki_syndrome_1|Kabuki_syndrome_2|not_provided": 1,
    "not_provided|Kabuki_syndrome_1|Kabuki_syndrome_2": 1,
    "Primary_dilated_cardiomyopathy|Intellectual_disability|KDM6A-related_disorder|Kabuki_syndrome_2": 1,
    "not_specified|Kabuki_syndrome_2|Inborn_genetic_diseases|not_provided|KDM6A-related_disorder": 1,
    "Kabuki_syndrome_2|Inborn_genetic_diseases": 11,
    "Kabuki_syndrome_2|not_provided|Kabuki_syndrome_1": 1,
    "KDM6A-related_disorder|not_provided": 3,
    "KDM6A-related_disorder|Kabuki_syndrome_2|not_provided": 2,
    "KDM6A-related_disorder|not_specified|Kabuki_syndrome_2": 1,
    "Kabuki_syndrome_2|Kabuki_syndrome_1": 1,
    "KDM6A-related_disorder|Kabuki_syndrome_2|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "Kabuki_syndrome_2|See_cases": 1,
    "Kabuki_syndrome_2|Kabuki_syndrome_1|not_provided|Inborn_genetic_diseases": 1,
    "KDM6A-related_disorder|not_provided|Kabuki_syndrome_2|not_specified": 2,
    "not_provided|Kabuki_syndrome_2|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Kabuki_syndrome_2|Intellectual_disability": 1,
    "Neurodevelopmental_disorder|Kabuki_syndrome_2|not_provided": 1,
    "KDM6A-related_disorder|Inborn_genetic_diseases|not_provided|Kabuki_syndrome_2": 1,
    "See_cases|Kabuki_syndrome_2": 1,
    "Tremor|_hereditary_essential|_6": 1,
    "Kabuki_syndrome_2|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Kabuki_syndrome_2": 2,
    "Kabuki_syndrome_2|KDM6A-related_disorder|not_provided": 1,
    "KDM6A-related_disorder|Kabuki_syndrome_2|not_specified": 2,
    "Kabuki_syndrome_1|Kabuki_syndrome_2": 2,
    "Inborn_genetic_diseases|Kabuki_syndrome_2|Intellectual_disability": 1,
    "not_provided|Kabuki_syndrome_2|not_specified": 2,
    "not_provided|not_specified|Kabuki_syndrome_2|Kabuki_syndrome_1": 1,
    "Intellectual_disability|Kabuki_syndrome_2|not_provided": 1,
    "not_provided|Kabuki_syndrome_2|Kabuki_syndrome_1": 1,
    "KDM6A-related_disorder|Inborn_genetic_diseases|Kabuki_syndrome_2": 1,
    "Kabuki_Syndrome_-_KDM6A|not_provided": 1,
    "Kabuki_syndrome_2|not_provided|KDM6A-related_disorder|not_specified": 1,
    "Intellectual_disability|Kabuki_syndrome_2": 1,
    "not_provided|KDM6A-related_disorder|Intellectual_disability|Inborn_genetic_diseases|Kabuki_syndrome_2": 1,
    "Kabuki_syndrome_2|Anemia": 1,
    "Inborn_genetic_diseases|not_provided|Kabuki_syndrome_2": 1,
    "DIPK2B-related_disorder": 7,
    "not_provided|DIPK2B-related_disorder": 1,
    "ZNF674-related_disorder": 5,
    "ZNF674-related_disorder|not_provided|not_specified": 1,
    "not_provided|not_specified|ZNF674-related_disorder": 1,
    "not_specified|ZNF674-related_disorder|not_provided": 1,
    "ZNF674-related_disorder|not_specified|not_provided": 2,
    "ZNF674-related_disorder|History_of_neurodevelopmental_disorder|not_specified": 1,
    "Intellectual_developmental_disorder|_X-linked_108": 17,
    "SLC9A7-related_disorder|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder|_X-linked_108|SLC9A7-related_disorder": 1,
    "not_specified|not_provided|Intellectual_developmental_disorder|_X-linked_108": 1,
    "SLC9A7-related_disorder": 2,
    "Intellectual_developmental_disorder|_X-linked_108|SLC9A7-related_neurodevelopmental_disorder|not_provided": 1,
    "not_provided|Intellectual_developmental_disorder|_X-linked_108": 1,
    "SLC9A7-related_disorder|not_provided|Intellectual_developmental_disorder|_X-linked_108": 1,
    "not_provided|Retinitis_pigmentosa_2": 7,
    "X-linked_retinitis_pigmentosa|not_provided|Retinitis_pigmentosa": 1,
    "Retinal_dystrophy|not_provided|Retinitis_pigmentosa_2": 3,
    "Cone-rod_dystrophy|not_provided|Macular_dystrophy|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_2|not_provided": 1,
    "Retinitis_pigmentosa|Retinitis_pigmentosa_2|not_specified": 1,
    "RP2-related_disorder|not_provided": 2,
    "Retinitis_pigmentosa_3|not_provided|Leber_congenital_amaurosis": 1,
    "Retinitis_pigmentosa_2": 19,
    "Retinitis_pigmentosa_3|not_specified|Retinitis_pigmentosa|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Retinitis_pigmentosa_2": 3,
    "X-linked_retinitis_pigmentosa|Retinitis_pigmentosa|Retinal_dystrophy|not_provided|Retinitis_pigmentosa_2": 1,
    "Retinal_dystrophy|Retinitis_pigmentosa_2|Retinitis_pigmentosa|not_provided": 1,
    "Retinitis_pigmentosa_2|Retinal_dystrophy|not_provided": 1,
    "Retinitis_pigmentosa_2|not_provided": 3,
    "not_provided|Retinitis_pigmentosa|Retinitis_pigmentosa_2": 1,
    "Retinitis_pigmentosa_2|not_provided|RP2-related_disorder": 1,
    "Retinitis_pigmentosa_2|Retinal_dystrophy": 1,
    "not_specified|not_provided|Retinitis_pigmentosa_2|Retinitis_pigmentosa": 1,
    "not_provided|Retinitis_pigmentosa_2|Retinitis_pigmentosa_3|Retinal_dystrophy": 1,
    "Retinitis_pigmentosa_2|not_provided|not_specified": 1,
    "NDUFB11-related_disorders": 2,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_30|Inborn_genetic_diseases": 1,
    "Linear_skin_defects_with_multiple_congenital_anomalies_3|NDUFB11-related_disorders": 1,
    "Linear_skin_defects_with_multiple_congenital_anomalies_3": 5,
    "Linear_skin_defects_with_multiple_congenital_anomalies_3|Mitochondrial_complex_I_deficiency|_nuclear_type_30|not_provided": 1,
    "not_provided|Mitochondrial_complex_I_deficiency|_nuclear_type_30": 2,
    "NDUFB11-related_disorders|not_provided": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_30": 2,
    "not_provided|Linear_skin_defects_with_multiple_congenital_anomalies_3|Mitochondrial_complex_I_deficiency|_nuclear_type_1|Linear_skin_defects_with_multiple_congenital_anomalies_1|Histiocytoid_cardiomyopathy": 1,
    "not_specified|NDUFB11-related_disorders": 1,
    "Inborn_genetic_diseases|NDUFB11-related_disorders": 1,
    "not_provided|RBM10-related_disorder": 6,
    "TARP_syndrome": 25,
    "RBM10-related_disorder": 4,
    "not_provided|Neurodevelopmental_delay|TARP_syndrome": 1,
    "RBM10-related_disorder|not_provided": 4,
    "TARP_syndrome|not_provided": 1,
    "not_provided|TARP_syndrome": 1,
    "Infantile-onset_X-linked_spinal_muscular_atrophy": 417,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder": 5,
    "not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy": 7,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|VEXAS_syndrome": 2,
    "not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy|VEXAS_syndrome|VEXAS": 1,
    "Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder|VEXAS_syndrome|VEXAS|not_provided": 1,
    "VEXAS_syndrome|Infantile-onset_X-linked_spinal_muscular_atrophy|VEXAS|not_provided|UBA1-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|not_specified": 3,
    "Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy": 28,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|Inborn_genetic_diseases": 33,
    "not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy": 17,
    "not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy|Inborn_genetic_diseases": 4,
    "UBA1-related_disorder|Inborn_genetic_diseases": 1,
    "VEXAS_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy": 2,
    "Inborn_genetic_diseases|not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy|not_specified": 2,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|VEXAS_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|not_provided": 10,
    "not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder": 1,
    "UBA1-related_disorder|Infantile-onset_X-linked_spinal_muscular_atrophy": 2,
    "not_specified|not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy|not_provided": 3,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|VEXAS_syndrome|not_provided": 1,
    "not_provided|not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy": 2,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder|not_specified": 1,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|UBA1-related_disorder|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy|Inborn_genetic_diseases": 2,
    "not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy|not_specified|VEXAS_syndrome|UBA1-related_disorder": 1,
    "not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy|not_provided": 2,
    "not_provided|Infantile-onset_X-linked_spinal_muscular_atrophy|not_specified": 3,
    "VEXAS_syndrome|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "UBA1-related_disorder": 3,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|not_provided|UBA1-related_disorder": 2,
    "Infantile-onset_X-linked_spinal_muscular_atrophy|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|UBA1-related_disorder|Infantile-onset_X-linked_spinal_muscular_atrophy": 1,
    "not_specified|Infantile-onset_X-linked_spinal_muscular_atrophy|UBA1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Infantile-onset_X-linked_spinal_muscular_atrophy|not_specified": 1,
    "CDK16-related_disorder": 7,
    "CDK16-related_Intellectual_Disability": 1,
    "CDK16-related_disorder|not_specified": 1,
    "not_provided|CDK16-related_disorder": 1,
    "Bronchiectasis|Dynein_arm_defect_of_respiratory_motile_cilia|Absent_inner_and_outer_dynein_arms|Abnormal_ciliary_motility": 1,
    "USP11-related_disorder": 1,
    "ZNF41-related_disorder": 3,
    "ZNF41-related_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|History_of_neurodevelopmental_disorder": 1,
    "not_specified|Global_developmental_delay|Seizure|Intellectual_disability": 1,
    "not_provided|not_specified|ZNF41-related_disorder": 1,
    "ZNF41-related_disorder|not_provided": 1,
    "not_provided|Non-syndromic_X-linked_intellectual_disability": 5,
    "ARAF-related_disorder": 1,
    "Lymphatic_anomaly": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 338,
    "not_specified|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 8,
    "not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Intellectual_disability|_X-linked_50": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_provided": 14,
    "Inborn_genetic_diseases|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 7,
    "not_specified|Inborn_genetic_diseases|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 3,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases|not_provided": 2,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|SYN1-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 21,
    "SYN1-related_disorder": 9,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|SYN1-related_disorder": 3,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases": 12,
    "SYN1-related_disorder|Inborn_genetic_diseases|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Intellectual_disability|_X-linked_50|History_of_neurodevelopmental_disorder|SYN1-related_disorder|not_provided|not_specified|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "not_provided|SYN1-related_disorder|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Intellectual_disability|_X-linked_50|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_provided": 2,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|SYN1-related_disorder|not_specified": 1,
    "not_provided|SYN1-related_disorder|Inborn_genetic_diseases|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 3,
    "SYN1-related_neurodevelopmental_disorder|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases": 1,
    "Seizure|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "not_provided|X-linked_complex_neurodevelopmental_disorder|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Intellectual_disability|_X-linked_50|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 3,
    "not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|History_of_neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases|not_specified": 1,
    "SYN1-related_disorder|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_provided|Intellectual_disability|_X-linked_50": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_provided|not_specified": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Epilepsy": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Intellectual_disability|_X-linked_50": 4,
    "SYN1-related_disorder|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Intellectual_disability|_X-linked_50": 4,
    "Inborn_genetic_diseases|not_specified|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 2,
    "not_specified|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases": 1,
    "not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|SYN1-related_disorder|not_specified": 1,
    "SYN1-related_disorder|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_specified": 1,
    "not_provided|not_specified|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|History_of_neurodevelopmental_disorder": 1,
    "not_specified|History_of_neurodevelopmental_disorder|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Inborn_genetic_diseases|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_provided": 2,
    "not_specified|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_specified": 1,
    "Intellectual_disability|Intellectual_disability|_X-linked_50": 1,
    "Intellectual_disability|_X-linked_50|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_50|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 2,
    "History_of_neurodevelopmental_disorder|not_provided|not_specified|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|Intellectual_disability|_X-linked_50": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "not_provided|Inborn_genetic_diseases|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "not_provided|Intellectual_disability|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders|not_provided|SYN1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|History_of_neurodevelopmental_disorder|Epilepsy|_X-linked_1|_with_variable_learning_disabilities_and_behavior_disorders": 1,
    "CFP-related_disorder": 1,
    "not_provided|CFP-related_disorder": 4,
    "Properdin_deficiency|_type_III": 1,
    "Properdin_deficiency|_X-linked": 5,
    "Properdin_deficiency|_X-linked|not_provided": 3,
    "CFP-related_disorder|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Properdin_deficiency|_X-linked": 1,
    "not_provided|Properdin_deficiency|_X-linked": 1,
    "not_provided|Properdin_deficiency|_type_II": 1,
    "not_provided|CFP-related_disorder|Properdin_deficiency|_X-linked": 1,
    "not_specified|History_of_neurodevelopmental_disorder|not_provided": 2,
    "ZNF81-related_disorder|History_of_neurodevelopmental_disorder|not_provided": 1,
    "ZNF81-related_disorder": 5,
    "not_provided|not_specified|ZNF81-related_disorder": 1,
    "Intellectual_disability|_X-linked_45": 1,
    "ZNF81-related_disorder|History_of_neurodevelopmental_disorder": 1,
    "not_specified|ZNF81-related_disorder": 1,
    "SSX1-related_disorder": 4,
    "Spermatogenic_failure|_X-linked|_5": 2,
    "Synovial_sarcoma": 1,
    "SSX1-related_disorder|not_provided": 1,
    "Spermatogenic_failure|_X-linked|_5|SSX1-related_disorder": 1,
    "SLC38A5-related_disorder": 1,
    "Intellectual_disability|_X-linked_9|not_provided": 1,
    "Intellectual_disability|_X-linked_9": 9,
    "Inborn_genetic_diseases|not_provided|FTSJ1-related_disorder": 1,
    "FTSJ1-related_disorder": 3,
    "Inborn_genetic_diseases|FTSJ1-related_disorder|not_provided": 2,
    "not_provided|Intellectual_disability|_X-linked_9": 1,
    "not_provided|FTSJ1-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_9": 1,
    "FTSJ1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Focal_dermal_hypoplasia": 31,
    "not_provided|Focal_dermal_hypoplasia": 5,
    "Focal_dermal_hypoplasia|Anophthalmia-microphthalmia_syndrome|not_provided": 1,
    "Focal_dermal_hypoplasia|not_provided": 5,
    "PORCN-related_disorder": 8,
    "Focal_dermal_hypoplasia|Inborn_genetic_diseases": 1,
    "PORCN-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Focal_dermal_hypoplasia": 1,
    "not_provided|PORCN-related_disorder|Inborn_genetic_diseases": 1,
    "PORCN-related_disorder|not_provided": 1,
    "PORCN-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Cleft_palate|Connective_tissue_disorder|not_specified": 1,
    "EBP-related_disorder|MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "MEND_syndrome|not_specified|Chondrodysplasia_punctata_2_X-linked_dominant|not_provided": 1,
    "Chondrodysplasia_punctata_2_X-linked_dominant|MEND_syndrome": 5,
    "Chondrodysplasia_punctata_2_X-linked_dominant|MEND_syndrome|not_provided": 3,
    "CHONDRODYSPLASIA_PUNCTATA_2|_X-LINKED_DOMINANT|_ATYPICAL": 1,
    "MEND_syndrome": 2,
    "Intellectual_disability|Connective_tissue_disorder|not_provided": 1,
    "Chondrodysplasia_punctata_2_X-linked_dominant": 39,
    "not_provided|EBP-related_disorder": 3,
    "MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant": 1,
    "not_provided|Chondrodysplasia_punctata_2_X-linked_dominant": 5,
    "Chondrodysplasia_punctata_2_X-linked_dominant|not_provided": 2,
    "not_specified|not_provided|Chondrodysplasia_punctata_2_X-linked_dominant|MEND_syndrome": 1,
    "MEND_syndrome|not_provided": 1,
    "Chondrodysplasia_punctata_2_X-linked_dominant|Connective_tissue_disorder|not_provided": 1,
    "MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant|Inborn_genetic_diseases": 1,
    "EBP-related_disorder|not_provided": 1,
    "not_provided|MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant": 2,
    "Inborn_genetic_diseases|EBP-related_disorder|not_specified|not_provided": 1,
    "not_provided|Chondrodysplasia_punctata_2_X-linked_dominant|MEND_syndrome": 1,
    "not_specified|not_provided|Chondrodysplasia_punctata_2_X-linked_dominant": 1,
    "not_provided|MEND_syndrome": 3,
    "MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant|not_provided": 1,
    "MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant|not_provided|not_specified|EBP-related_disorder": 1,
    "EBP-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Chondrodysplasia_punctata_2_X-linked_dominant|not_specified": 1,
    "Inborn_genetic_diseases|MEND_syndrome|Chondrodysplasia_punctata_2_X-linked_dominant|not_specified|not_provided": 1,
    "Wiskott-Aldrich_syndrome": 47,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome": 95,
    "Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 84,
    "Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|not_specified": 7,
    "Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 222,
    "Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|not_provided": 6,
    "not_provided|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 10,
    "not_specified|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome": 5,
    "Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia": 25,
    "not_provided|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|not_specified|WAS-related_disorder": 1,
    "not_provided|Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia": 1,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|WAS-related_disorder": 4,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|Inborn_genetic_diseases|WAS-related_disorder": 1,
    "WAS-related_disorder": 3,
    "WAS-related_disorder|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|not_provided|Thrombocytopenia": 1,
    "Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome": 10,
    "not_specified|Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia": 1,
    "Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|not_provided": 2,
    "not_provided|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome": 3,
    "THROMBOCYTOPENIA|_X-LINKED|_INTERMITTENT": 2,
    "X-linked_severe_congenital_neutropenia": 3,
    "Inborn_genetic_diseases|not_provided|WAS-related_disorder|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 1,
    "Wiskott-Aldrich_syndrome|not_specified|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 1,
    "Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|not_provided": 3,
    "WISKOTT-ALDRICH_SYNDROME|_ATTENUATED|not_provided": 1,
    "WAS-related_disorder|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome": 2,
    "WAS-related_disorder|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|not_provided": 1,
    "not_provided|not_specified|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 1,
    "not_specified|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|not_provided": 1,
    "not_provided|not_specified|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome": 2,
    "X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|Thrombocytopenia_1": 9,
    "Inborn_genetic_diseases|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome": 3,
    "not_specified|Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|not_provided": 1,
    "not_provided|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome": 5,
    "not_specified|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 2,
    "WAS-related_disorder|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|not_specified|not_provided": 1,
    "WAS-related_disorder|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|not_specified|not_provided": 1,
    "Thrombocytopenia_1": 7,
    "not_provided|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|not_specified": 2,
    "not_specified|not_provided|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 1,
    "not_provided|Thrombocytopenia_1": 1,
    "Inborn_genetic_diseases|not_specified|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 1,
    "Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|not_specified": 1,
    "WAS-related_disorder|not_specified|Thrombocytopenia_1|not_provided|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 1,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 4,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|not_provided": 9,
    "not_provided|Wiskott-Aldrich_syndrome": 1,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Wiskott-Aldrich_syndrome|Thrombocytopenia": 1,
    "WAS-related_disorder|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia": 2,
    "not_provided|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|Thrombocytopenia_1": 1,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-Linked_Neutropenia|WAS-related_disorder|not_provided": 1,
    "Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Inborn_genetic_diseases": 2,
    "Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|WAS-related_disorder": 2,
    "Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|Inborn_genetic_diseases": 1,
    "Wiskott-Aldrich_syndrome|not_provided|not_specified|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 1,
    "Wiskott-Aldrich_syndrome|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Inborn_genetic_diseases": 1,
    "X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome": 1,
    "not_specified|not_provided|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|Thrombocytopenia_1": 1,
    "Inborn_genetic_diseases|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|not_provided": 1,
    "not_provided|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Wiskott-Aldrich_syndrome|WAS-related_disorder": 1,
    "not_specified|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 2,
    "WAS-related_disorder|not_provided|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 1,
    "not_specified|WAS-related_disorder|Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome": 1,
    "Inborn_genetic_diseases|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1": 1,
    "Thrombocytopenia_1|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|not_provided|WAS-related_disorder": 1,
    "Wiskott-Aldrich_syndrome|not_provided|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|not_specified": 1,
    "Thrombocytopenia_1|X-linked_severe_congenital_neutropenia|Wiskott-Aldrich_syndrome|not_provided": 1,
    "not_specified|Wiskott-Aldrich_syndrome|X-linked_severe_congenital_neutropenia|Thrombocytopenia_1|Thrombocytopenia|Abnormal_bleeding": 1,
    "Ependymoma|not_specified": 1,
    "GATA1-related_disorder": 12,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 138,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 1,
    "Transient_myeloproliferative_syndrome": 4,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia": 92,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Down_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|GATA1-related_disorder": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Acute_megakaryoblastic_leukemia_in_down_syndrome": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|not_specified": 2,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|not_provided|Down_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|not_provided|GATA1-related_disorder|not_specified": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|not_provided": 4,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Acute_megakaryoblastic_leukemia": 1,
    "Inborn_genetic_diseases|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia": 3,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|GATA1-related_disorder": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|GATA1-related_disorder|not_specified|not_provided": 1,
    "X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 3,
    "not_provided|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 9,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Down_syndrome|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|not_specified": 1,
    "LEUKEMIA|_MEGAKARYOBLASTIC|_OF_DOWN_SYNDROME|_SOMATIC": 1,
    "Inborn_genetic_diseases|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|GATA1-related_disorder": 1,
    "not_specified|not_provided|GATA1-related_disorder|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 2,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|not_provided": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 1,
    "not_provided|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia": 9,
    "Down_syndrome|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia": 1,
    "Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Transient_myeloproliferative_syndrome|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Inborn_genetic_diseases": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|not_provided": 2,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Transient_myeloproliferative_syndrome|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|GATA1-related_disorder": 3,
    "Inborn_genetic_diseases|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 2,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Inborn_genetic_diseases": 4,
    "Beta-thalassemia-X-linked_thrombocytopenia_syndrome|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Transient_myeloproliferative_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|Beta-thalassemia-X-linked_thrombocytopenia_syndrome": 2,
    "Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Transient_myeloproliferative_syndrome|Beta-thalassemia-X-linked_thrombocytopenia_syndrome": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|Transient_myeloproliferative_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|not_provided": 1,
    "not_provided|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|not_specified": 1,
    "Down_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Thrombocytopenia|_X-linked|_with_dyserythropoietic_anemia": 2,
    "Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia": 4,
    "Thrombocytopenia|_X-linked|_without_dyserythropoietic_anemia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|GATA1-related_disorder|not_provided|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|Cutaneous_porphyria": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|not_provided|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome": 1,
    "Macrothrombocytopenia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia": 1,
    "Thrombocytopenia|_X-linked|_without_dyserythropoietic_anemia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Thrombocytopenia": 1,
    "Anemia|Thrombocytopenia": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|Transient_myeloproliferative_syndrome": 1,
    "Macrothrombocytopenia|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|not_specified|GATA1-related_disorder": 1,
    "not_provided|not_specified|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "Down_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "not_specified|Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "Hemolytic_anemia_due_to_erythrocyte_adenosine_deaminase_overproduction|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Down_syndrome|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia|Beta-thalassemia-X-linked_thrombocytopenia_syndrome|X-linked_dyserythropoetic_anemia_with_abnormal_platelets_and_neutropenia": 1,
    "Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_specified|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "GATA1-related_disorder|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "GATA1-related_disorder|not_provided|Inborn_genetic_diseases|Diamond-Blackfan_anemia|GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis": 1,
    "GATA_binding_protein_1_related_thrombocytopenia_with_dyserythropoiesis|Diamond-Blackfan_anemia|not_specified": 1,
    "Thrombocytopenia|Thrombocytopenia|_X-linked|_with_or_without_dyserythropoietic_anemia": 1,
    "X-linked_dominant_chondrodysplasia|_Chassaing-Lacombe_type|not_specified|not_provided": 1,
    "X-linked_dominant_chondrodysplasia|_Chassaing-Lacombe_type": 6,
    "not_provided|HDAC6-related_disorder": 3,
    "not_provided|X-linked_dominant_chondrodysplasia|_Chassaing-Lacombe_type": 2,
    "HDAC6-related_disorder": 6,
    "not_specified|Usher_syndrome": 1,
    "X-linked_dominant_chondrodysplasia|_Chassaing-Lacombe_type|not_provided": 1,
    "HDAC6-related_disorder|not_specified|not_provided": 1,
    "HDAC6-related_disorder|not_provided": 2,
    "not_provided|not_specified|X-linked_dominant_chondrodysplasia|_Chassaing-Lacombe_type": 1,
    "HDAC6-related_disorder|not_specified": 1,
    "Renpenning_syndrome": 26,
    "Renpenning_syndrome|not_provided": 2,
    "History_of_neurodevelopmental_disorder|not_specified|Renpenning_syndrome|not_provided": 1,
    "PQBP1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Renpenning_syndrome": 1,
    "not_provided|Renpenning_syndrome": 6,
    "PQBP1-related_disorder|not_specified|not_provided|Renpenning_syndrome": 1,
    "Inborn_genetic_diseases|Renpenning_syndrome": 1,
    "not_provided|PQBP1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|PQBP1-related_disorder": 2,
    "Inborn_genetic_diseases|not_provided|Renpenning_syndrome|PQBP1-related_disorder": 1,
    "PQBP1-related_disorder": 2,
    "PQBP1-related_disorder|not_provided|Renpenning_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Renpenning_syndrome|Microcephaly|Hyperactivity|Delayed_speech_and_language_development|See_cases|Intellectual_disability": 1,
    "Renpenning_syndrome|Inborn_genetic_diseases": 2,
    "Renpenning_syndrome|not_specified|not_provided": 1,
    "PQBP1-related_disorder|Renpenning_syndrome": 1,
    "Intellectual_disability|_mild|not_provided|Inborn_genetic_diseases": 1,
    "PQBP1-related_disorder|Renpenning_syndrome|not_provided": 1,
    "not_provided|Renpenning_syndrome|PQBP1-related_disorder|Intellectual_disability": 1,
    "not_specified|Renpenning_syndrome": 1,
    "Autism_spectrum_disorder|not_provided|Renpenning_syndrome": 1,
    "Renpenning_syndrome|Intellectual_disability": 1,
    "Renpenning_syndrome|History_of_neurodevelopmental_disorder": 1,
    "Inborn_genetic_diseases|SLC35A2-congenital_disorder_of_glycosylation": 5,
    "SLC35A2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases": 11,
    "not_provided|SLC35A2-congenital_disorder_of_glycosylation": 11,
    "SLC35A2-congenital_disorder_of_glycosylation|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SLC35A2-related_disorder|not_provided|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|SLC35A2-congenital_disorder_of_glycosylation|not_specified|not_provided": 1,
    "not_specified|SLC35A2-congenital_disorder_of_glycosylation": 2,
    "Autism|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "SLC35A2-congenital_disorder_of_glycosylation|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "SLC35A2-congenital_disorder_of_glycosylation|not_provided": 20,
    "SLC35A2-congenital_disorder_of_glycosylation|not_specified": 1,
    "SLC35A2-related_disorder|not_provided|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "SLC35A2-congenital_disorder_of_glycosylation|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|SLC35A2-congenital_disorder_of_glycosylation|not_provided": 2,
    "non-lesional_focal_epilepsy": 4,
    "Inborn_genetic_diseases|not_provided|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|SLC35A2-congenital_disorder_of_glycosylation|SLC35A2-related_disorder|not_provided": 1,
    "SLC35A2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_provided": 1,
    "non-lesional_focal_epilepsy|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "SLC35A2-related_disorder|SLC35A2-congenital_disorder_of_glycosylation": 2,
    "SLC35A2-congenital_disorder_of_glycosylation|Inborn_genetic_diseases|not_specified": 1,
    "SLC35A2-congenital_disorder_of_glycosylation|not_provided|not_specified": 1,
    "SLC35A2-related_disorder|See_cases": 1,
    "SLC35A2-related_disorder": 5,
    "Inborn_genetic_diseases|not_specified|SLC35A2-congenital_disorder_of_glycosylation": 1,
    "SLC35A2-congenital_disorder_of_glycosylation|SLC35A2-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|SLC35A2-congenital_disorder_of_glycosylation|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|SLC35A2-related_disorder|SLC35A2-congenital_disorder_of_glycosylation|not_provided": 1,
    "not_provided|X-linked_complex_neurodevelopmental_disorder": 1,
    "Multiple_congenital_anomalies-neurodevelopmental_syndrome|_X-linked": 14,
    "Multiple_congenital_anomalies-neurodevelopmental_syndrome|_X-linked|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Multiple_congenital_anomalies-neurodevelopmental_syndrome|_X-linked": 1,
    "Abnormal_cerebral_cortex_morphology|Dysplastic_corpus_callosum": 1,
    "OTUD5-related_disorder": 6,
    "Neurodegeneration_with_brain_iron_accumulation_5": 332,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-neurodevelopmental_syndrome|_X-linked": 1,
    "not_specified|OTUD5-related_disorder": 1,
    "Inborn_genetic_diseases|Multiple_congenital_anomalies-neurodevelopmental_syndrome|_X-linked|not_provided": 1,
    "not_specified|KCND1-associated_seizure_disorder": 1,
    "Renal_cell_carcinoma|_Xp11-associated": 1,
    "not_provided|Intellectual_developmental_disorder|_X-linked|_syndromic|_with_pigmentary_mosaicism_and_coarse_facies|Renal_cell_carcinoma|_Xp11-associated": 1,
    "TFE3-related_disorder": 5,
    "not_provided|Renal_cell_carcinoma|_Xp11-associated": 1,
    "TFE3-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|TFE3-related_disorder": 1,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_with_pigmentary_mosaicism_and_coarse_facies": 18,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_with_pigmentary_mosaicism_and_coarse_facies|Renal_cell_carcinoma|Neurodevelopmental_abnormality|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_with_pigmentary_mosaicism_and_coarse_facies|not_provided": 1,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_with_pigmentary_mosaicism_and_coarse_facies|Neurodevelopmental_disorder|not_provided": 1,
    "TFE3-Associated_Neurodevelopmental_disorder": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_5": 18,
    "Neurodegeneration_with_brain_iron_accumulation_5|Inborn_genetic_diseases": 4,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_provided|See_cases": 2,
    "WDR45-related_disorder": 5,
    "not_provided|not_specified|Neurodegeneration_with_brain_iron_accumulation_5": 3,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_provided": 33,
    "Neurodegeneration_with_brain_iron_accumulation_5|WDR45-related_disorder": 1,
    "not_specified|Neurodegeneration_with_brain_iron_accumulation_5|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Neurodegeneration_with_brain_iron_accumulation_5|not_provided": 2,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_5": 10,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_specified": 4,
    "not_specified|Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_5|not_provided|Oculocutaneous_albinism_type_7": 1,
    "not_specified|Neurodegeneration_with_brain_iron_accumulation_5": 7,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation|Neurodegeneration_with_brain_iron_accumulation_5": 1,
    "Intellectual_disability|Neurodegeneration_with_brain_iron_accumulation_5": 1,
    "Neurodegeneration_with_brain_iron_accumulation_5|Seizure|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Global_developmental_delay|Delayed_gross_motor_development|Hypoplasia_of_the_corpus_callosum|Absent_speech|Delayed_speech_and_language_development|Seizure|Neurodegeneration_with_brain_iron_accumulation_5|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_provided|Intellectual_disability": 2,
    "Neurodegeneration_with_brain_iron_accumulation_5|Oculocutaneous_albinism_type_7": 1,
    "Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_5|not_provided|not_specified": 1,
    "X-linked_cerebral-cerebellar-coloboma_syndrome_syndrome|Inborn_genetic_diseases|not_provided|Neurodegeneration_with_brain_iron_accumulation_5": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_5|not_specified|Inborn_genetic_diseases": 1,
    "Neurodegeneration_with_brain_iron_accumulation_5|WDR45-related_disorder|not_provided": 1,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Neurodegeneration_with_brain_iron_accumulation_5|Oculocutaneous_albinism_type_7": 1,
    "not_provided|Inborn_genetic_diseases|Neurodegeneration_with_brain_iron_accumulation_5": 2,
    "Optic_atrophy_2": 2,
    "Seizure|Autism|Global_developmental_delay": 1,
    "X-linked_cerebral-cerebellar-coloboma_syndrome_syndrome|Neurodegeneration_with_brain_iron_accumulation_5": 1,
    "X-linked_cerebral-cerebellar-coloboma_syndrome_syndrome": 1,
    "not_provided|not_specified|WDR45-related_disorder|Neurodegeneration_with_brain_iron_accumulation_5": 1,
    "Dystonic_disorder|Basal_ganglia_calcification": 1,
    "Neurodegeneration_with_brain_iron_accumulation_5|not_specified|not_provided": 1,
    "WDR45-related_disorder|not_provided|Neurodegeneration_with_brain_iron_accumulation_5": 1,
    "Inborn_genetic_diseases|Oculocutaneous_albinism_type_7|Neurodegeneration_with_brain_iron_accumulation_5|Global_developmental_delay|not_provided": 1,
    "GPKOW-related_disorder": 4,
    "not_specified|GPKOW-related_disorder": 1,
    "Holoprosencephaly-hypokinesia-congenital_contractures_syndrome": 2,
    "GPKOW-related_disorder|not_provided": 1,
    "not_provided|GPKOW-related_disorder": 1,
    "Intellectual_disability|_X-linked_96": 17,
    "History_of_neurodevelopmental_disorder|not_provided|Charcot-Marie-Tooth_disease|not_specified": 1,
    "not_provided|Intellectual_disability|_X-linked_96": 1,
    "SYP-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_96": 1,
    "Congenital_stationary_night_blindness_2A|not_provided": 3,
    "CACNA1F-related_disorder|not_provided": 18,
    "not_provided|Aland_island_eye_disease": 1,
    "not_provided|Congenital_stationary_night_blindness_2A": 4,
    "not_provided|Aland_island_eye_disease|Congenital_stationary_night_blindness_2A|X-linked_cone-rod_dystrophy_3|Inborn_genetic_diseases": 1,
    "Congenital_stationary_night_blindness_2A": 19,
    "Congenital_stationary_night_blindness_2A|Retinal_dystrophy|not_provided": 1,
    "Cone-rod_dystrophy|Congenital_stationary_night_blindness_2A|Optic_atrophy": 1,
    "not_provided|CACNA1F-related_disorder": 8,
    "Aland_island_eye_disease|not_provided": 2,
    "CACNA1F-related_disorder|not_provided|not_specified": 1,
    "Congenital_stationary_night_blindness|Optic_atrophy|X-linked_cone-rod_dystrophy_3|not_provided": 1,
    "Congenital_stationary_night_blindness|Congenital_stationary_night_blindness_2A": 1,
    "Progressive_cone_dystrophy_(without_rod_involvement)|Retinal_dystrophy": 1,
    "X-linked_cone-rod_dystrophy_3": 11,
    "not_provided|Congenital_stationary_night_blindness_2A|X-linked_cone-rod_dystrophy_3|Aland_island_eye_disease": 1,
    "Inborn_genetic_diseases|not_provided|Abnormality_of_the_eye": 1,
    "Congenital_stationary_night_blindness_2A|Retinal_dystrophy": 1,
    "Congenital_stationary_night_blindness_2A|not_provided|Retinal_dystrophy|CACNA1F-related_disorder": 1,
    "Aland_island_eye_disease|Congenital_stationary_night_blindness_2A|X-linked_cone-rod_dystrophy_3": 2,
    "not_provided|Congenital_stationary_night_blindness_2A|X-linked_cone-rod_dystrophy_3": 1,
    "Retinal_dystrophy|Congenital_stationary_night_blindness|CACNA1F-related_disorder|not_provided|Congenital_stationary_night_blindness_2A": 1,
    "not_provided|CACNA1F-related_retinopathy|CACNA1F-related_disorder": 1,
    "not_specified|not_provided|Congenital_stationary_night_blindness_2A|X-linked_cone-rod_dystrophy_3|Aland_island_eye_disease": 1,
    "Congenital_stationary_night_blindness|Congenital_stationary_night_blindness_2A|not_provided": 1,
    "X-linked_cone-rod_dystrophy_3|Congenital_stationary_night_blindness_2A|Aland_island_eye_disease|not_provided|CACNA1F-related_disorder": 1,
    "CACNA1F-related_disorder": 8,
    "CACNA1F-related_disorder|not_specified|not_provided": 1,
    "not_specified|CACNA1F-related_disorder|not_provided": 1,
    "Aland_island_eye_disease|Congenital_stationary_night_blindness_2A|not_provided|X-linked_cone-rod_dystrophy_3": 1,
    "not_provided|Congenital_stationary_night_blindness|_type_2A|_severe": 1,
    "CACNA1F-related_disorder|not_specified|X-linked_cone-rod_dystrophy_3|Aland_island_eye_disease|Congenital_stationary_night_blindness_2A|not_provided|Cone-rod_dystrophy": 1,
    "X-linked_cone-rod_dystrophy_3|not_provided": 1,
    "X-linked_cone-rod_dystrophy_3|Congenital_stationary_night_blindness|not_provided": 1,
    "X-linked_cone-rod_dystrophy_3|Congenital_stationary_night_blindness_2A": 1,
    "not_specified|Retinal_dystrophy|not_provided|Congenital_stationary_night_blindness_2A": 1,
    "not_provided|X-linked_cone-rod_dystrophy_3|Aland_island_eye_disease|Congenital_stationary_night_blindness_2A": 1,
    "CACNA1F-related_disorder|Aland_island_eye_disease|X-linked_cone-rod_dystrophy_3|Congenital_stationary_night_blindness_2A|not_provided|Abnormality_of_neuronal_migration": 1,
    "not_specified|Congenital_stationary_night_blindness_2A|not_provided": 1,
    "Congenital_stationary_night_blindness_2A|Aland_island_eye_disease|X-linked_cone-rod_dystrophy_3|Cone-rod_dystrophy": 1,
    "X-linked_cone-rod_dystrophy_3|Aland_island_eye_disease|Congenital_stationary_night_blindness_2A|not_provided|not_specified": 1,
    "Cone-rod_dystrophy|not_provided|Congenital_stationary_night_blindness": 1,
    "Amblyopia|Myopia|Congenital_stationary_night_blindness_2A": 1,
    "Congenital_stationary_night_blindness_2A|Aland_island_eye_disease|not_provided|Retinal_dystrophy": 1,
    "Retinal_dystrophy|not_provided|Aland_island_eye_disease|Cone-rod_dystrophy": 1,
    "Ritscher-Schinzel_syndrome_2|CCDC22-related_disorder": 1,
    "Ritscher-Schinzel_syndrome_2|Ritscher-Schinzel_syndrome_1": 1,
    "CCDC22-related_disorder": 7,
    "Ritscher-Schinzel_syndrome_2": 21,
    "Ritscher-Schinzel_syndrome_2|not_specified|not_provided": 3,
    "not_provided|Ritscher-Schinzel_syndrome_2": 3,
    "CCDC22-related_disorder|not_provided": 1,
    "Ritscher-Schinzel_syndrome_2|not_specified": 2,
    "Ritscher-Schinzel_syndrome_2|not_provided": 2,
    "not_provided|CCDC22-related_disorder|not_specified": 1,
    "Ritscher-Schinzel_syndrome_2|not_specified|not_provided|Intellectual_disability": 1,
    "not_specified|Ritscher-Schinzel_syndrome_2": 3,
    "Obesity|not_specified": 1,
    "CCDC22-related_disorder|not_specified|not_provided|Intellectual_disability": 1,
    "CCDC22-related_disorder|Ritscher-Schinzel_syndrome_2": 1,
    "not_specified|not_provided|Ritscher-Schinzel_syndrome_2": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Intellectual_disability": 1,
    "Ritscher-Schinzel_syndrome_1|Ritscher-Schinzel_syndrome_2": 1,
    "not_specified|not_provided|CCDC22-related_disorder": 1,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 270,
    "not_provided|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 17,
    "FOXP3-related_disorder|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 2,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|not_provided": 11,
    "FOXP3-related_disorder|not_provided|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 1,
    "Hydrops_fetalis|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 1,
    "FOXP3-related_disorder": 5,
    "not_specified|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 3,
    "not_provided|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|Neurodevelopmental_disorder": 1,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|not_specified": 3,
    "Inborn_genetic_diseases|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 7,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|Inborn_genetic_diseases": 9,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|not_specified|not_provided": 1,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|FOXP3-related_disorder": 2,
    "Monogenic_diabetes|not_provided|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 1,
    "not_specified|Diabetes_mellitus_type_1": 1,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|FOXP3-related_disorder|not_specified": 1,
    "Monogenic_diabetes|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome": 1,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|not_specified|Monogenic_diabetes": 1,
    "not_specified|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|Non-obstructive_azoospermia|FOXP3-related_disorder": 1,
    "not_specified|Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|FOXP3-related_disorder": 1,
    "Insulin-dependent_diabetes_mellitus_secretory_diarrhea_syndrome|Diabetes_mellitus_type_1": 1,
    "PPP1R3F_Associated_Neurodevelopmental_Disorder": 1,
    "Intellectual_disability|_X-linked_105|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_105": 16,
    "Neurodevelopmental_disorder|Intellectual_disability|_X-linked_105": 1,
    "USP27X-related_disorder": 2,
    "USP27X-related_disorder|not_provided": 1,
    "Dent_disease_type_1": 125,
    "CLCN5-related_disorder": 9,
    "Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|X-linked_recessive_nephrolithiasis_with_renal_failure": 1,
    "Dent_disease|not_provided": 1,
    "Dent_disease": 18,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure": 36,
    "Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|not_provided": 1,
    "not_provided|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|not_provided": 3,
    "not_provided|Dent_disease_type_1|Familial_X-linked_hypophosphatemic_vitamin_D_refractory_rickets|CLCN5-related_disorder": 1,
    "not_provided|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Inborn_genetic_diseases": 1,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 5,
    "not_provided|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1": 1,
    "X-linked_recessive_nephrolithiasis_with_renal_failure": 3,
    "not_provided|Dent_disease_type_1": 17,
    "not_provided|Inborn_genetic_diseases|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Dent_disease_type_1|CLCN5-related_disorder": 1,
    "Hypophosphataemia|_X-linked": 1,
    "not_provided|CLCN5-related_disorder": 2,
    "Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Inborn_genetic_diseases|not_provided": 1,
    "CLCN5-related_disorder|not_provided": 2,
    "not_provided|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Dent_disease_type_1": 1,
    "not_provided|Nephrotic_syndrome|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|not_provided": 3,
    "not_provided|Inborn_genetic_diseases|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "not_provided|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure": 1,
    "Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "Dent_disease_type_1|not_provided|Hypophosphatemic_rickets|_X-linked_recessive|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|CLCN5-related_disorder": 1,
    "not_provided|Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure": 2,
    "Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure": 1,
    "Dent_disease_type_1|not_provided": 1,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1": 1,
    "Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|not_provided": 1,
    "X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Dent_disease": 4,
    "not_provided|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure": 1,
    "not_provided|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "not_specified|not_provided|Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure": 1,
    "not_provided|X-linked_recessive_nephrolithiasis_with_renal_failure|Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|not_provided": 2,
    "Hypophosphatemic_rickets|_X-linked_recessive|not_provided|CLCN5-related_disorder": 1,
    "Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure": 2,
    "not_provided|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Inborn_genetic_diseases": 1,
    "Hyperkalemia|Multiple_small_medullary_renal_cysts|Low-molecular-weight_proteinuria": 1,
    "Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive": 3,
    "Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "not_provided|not_specified|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1|Inborn_genetic_diseases|CLCN5-related_disorder": 1,
    "Hypophosphatemic_rickets|_X-linked_recessive|X-linked_recessive_nephrolithiasis_with_renal_failure|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "Inborn_genetic_diseases|not_provided|Dent_disease_type_1": 1,
    "Hypophosphatemic_rickets|_X-linked_recessive": 1,
    "not_specified|not_provided|Dent_disease": 1,
    "Inborn_genetic_diseases|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|not_provided": 1,
    "Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|not_provided|Dent_disease": 1,
    "Dent_disease_type_1|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|X-linked_recessive_nephrolithiasis_with_renal_failure|Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive|not_provided": 1,
    "Dent_disease_type_1|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Hypophosphatemic_rickets|_X-linked_recessive|not_provided": 1,
    "not_provided|X-linked_recessive_nephrolithiasis_with_renal_failure|Hypophosphatemic_rickets|_X-linked_recessive|Dent_disease_type_1|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Inborn_genetic_diseases": 1,
    "Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis|Dent_disease_type_1|CLCN5-related_disorder|X-linked_recessive_nephrolithiasis_with_renal_failure": 1,
    "Dent_disease_type_1|Hypophosphatemic_rickets|_X-linked_recessive|X-linked_recessive_nephrolithiasis_with_renal_failure|Proteinuria|_low_molecular_weight|_with_hypercalciuria_and_nephrocalcinosis": 1,
    "Pregnancy_loss|_recurrent|_susceptibility_to|_1": 1,
    "X-linked_intellectual_disability|_Stocco_dos_Santos_type": 27,
    "SHROOM4-related_disorder": 17,
    "not_provided|SHROOM4-related_disorder|not_specified": 1,
    "not_provided|not_specified|See_cases|Intellectual_disability": 1,
    "X-linked_intellectual_disability|_Stocco_dos_Santos_type|not_specified": 6,
    "not_provided|SHROOM4-related_disorder": 1,
    "not_specified|not_provided|X-linked_intellectual_disability|_Stocco_dos_Santos_type": 2,
    "SHROOM4-related_disorder|not_specified|not_provided": 3,
    "not_specified|X-linked_intellectual_disability|_Stocco_dos_Santos_type": 3,
    "not_specified|SHROOM4-related_disorder": 4,
    "X-linked_intellectual_disability|_Stocco_dos_Santos_type|not_provided": 1,
    "SHROOM4-related_disorder|not_provided": 1,
    "X-linked_intellectual_disability|_Stocco_dos_Santos_type|not_specified|not_provided": 1,
    "SHROOM4-related_disorder|not_specified": 2,
    "SHROOM4-related_disorder|not_provided|X-linked_intellectual_disability|_Stocco_dos_Santos_type": 1,
    "Ovarian_dysgenesis_2": 12,
    "not_provided|Ovarian_dysgenesis_2|not_specified": 3,
    "not_provided|not_specified|Ovarian_dysgenesis_2": 1,
    "Ovarian_dysgenesis_2|not_provided": 3,
    "BMP15-related_disorder|not_provided|Ovarian_dysgenesis_2|Premature_ovarian_failure_4": 1,
    "Premature_ovarian_failure_4|Ovarian_dysgenesis_2": 2,
    "not_specified|Ovarian_dysgenesis_2|not_provided": 1,
    "BMP15-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Ovarian_dysgenesis_2": 1,
    "not_provided|BMP15-related_disorder|Ovarian_dysgenesis_2": 1,
    "Ovarian_dysgenesis_2|BMP15-related_disorder": 1,
    "Premature_ovarian_failure_4": 1,
    "BMP15-related_disorder": 1,
    "Ovarian_dysgenesis|not_specified|not_provided": 1,
    "Ovarian_dysgenesis_2|Inborn_genetic_diseases": 1,
    "Ovarian_dysgenesis_2|not_specified": 1,
    "GSPT2-related_disorder": 1,
    "Seizure|Delayed_speech_and_language_development|Autism": 1,
    "MAGED1-related_neurodevelopmental_delay": 1,
    "KDM5C-related_disorder": 10,
    "KDM5C-related_disorder|not_provided": 4,
    "Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 109,
    "Inborn_genetic_diseases|KDM5C-related_disorder|not_provided": 1,
    "Spastic_paraplegia|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Spastic_paraplegia": 1,
    "Spastic_paraplegia|KDM5C-related_disorder": 3,
    "Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_provided": 7,
    "not_specified|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 3,
    "Inborn_genetic_diseases|Spastic_paraplegia|KDM5C-related_disorder|not_specified|not_provided|Intellectual_disability": 1,
    "Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_provided|Inborn_genetic_diseases": 1,
    "KDM5C-related_X-linked_syndromic_intellectual_disability": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 10,
    "Spastic_paraplegia|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "KDM5C-related_disorder|Spastic_paraplegia|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Spastic_paraplegia|not_provided|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_provided": 1,
    "Spastic_paraplegia|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 5,
    "KDM5C-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|KDM5C-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|KDM5C-related_disorder|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Spastic_paraplegia": 1,
    "Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Inborn_genetic_diseases": 4,
    "Rare_genetic_intellectual_disability|Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Spastic_paraplegia": 1,
    "Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Intellectual_disability|Hirsutism": 1,
    "Smith-Magenis_Syndrome-like|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 1,
    "X-linked_syndromic_intellectual_disability|not_provided|Spastic_paraplegia": 1,
    "Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|Spastic_paraplegia": 4,
    "Spastic_paraplegia|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_provided": 2,
    "Spastic_paraplegia|not_specified|not_provided|KDM5C-related_disorder": 1,
    "not_provided|Spastic_paraplegia|KDM5C-related_disorder": 1,
    "Spastic_paraplegia|not_provided|Inborn_genetic_diseases|KDM5C-related_disorder|not_specified": 1,
    "Developmental_disorder|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_provided|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|Spastic_paraplegia|not_provided": 2,
    "not_specified|Spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|KDM5C-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "KDM5C-related_disorder|Spastic_paraplegia|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 1,
    "not_specified|Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 1,
    "Inborn_genetic_diseases|not_specified|Spastic_paraplegia|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type|not_provided": 1,
    "KDM5C-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Spastic_paraplegia": 1,
    "Spastic_paraplegia|KDM5C-related_disorder|not_provided": 1,
    "not_specified|KDM5C-related_disorder|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "not_provided|Intellectual_disability|_X-linked_1": 57,
    "Intellectual_disability|_X-linked_1": 735,
    "Intellectual_disability|_X-linked_1|not_provided": 60,
    "IQSEC2-related_disorder": 12,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_X-linked_1": 3,
    "not_specified|not_provided|Intellectual_disability|_X-linked_1": 3,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_1": 5,
    "not_specified|Intellectual_disability|_X-linked_1|IQSEC2-related_disorder": 2,
    "Intellectual_disability|_X-linked_1|IQSEC2-related_disorder": 5,
    "Intellectual_disability|_X-linked_1|Inborn_genetic_diseases": 13,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_1": 17,
    "not_specified|Intellectual_disability|_X-linked_1": 17,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_X-linked_1|not_provided": 1,
    "not_specified|Intellectual_disability|_X-linked_1|not_provided": 3,
    "Intellectual_disability|_X-linked_1|not_specified": 14,
    "not_specified|Inborn_genetic_diseases|Intellectual_disability|_X-linked_1|IQSEC2-related_disorder|not_provided": 1,
    "Intellectual_disability|_X-linked_1|not_provided|See_cases": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_1": 6,
    "Intellectual_disability|_X-linked_1|Inborn_genetic_diseases|not_provided": 3,
    "Intellectual_disability|_X-linked_1|not_provided|Inborn_genetic_diseases": 4,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_X-linked_1": 5,
    "Intellectual_disability|_X-linked_1|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "IQSEC2-related_disorder|Intellectual_disability|_X-linked_1": 4,
    "IQSEC2-related_disorder|Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_1": 1,
    "not_provided|See_cases|Intellectual_disability|_X-linked_1": 1,
    "Inborn_genetic_diseases|not_provided|Abnormal_brain_morphology|not_specified|Intellectual_disability|_X-linked_1": 1,
    "not_provided|Intellectual_disability|_X-linked_1|Inborn_genetic_diseases": 8,
    "not_specified|Intellectual_disability|_X-linked_1|Specific_learning_disability|Involuntary_movements|not_provided": 1,
    "Intellectual_disability|_X-linked_1|Paraplegia-intellectual_disability-hyperkeratosis_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_1|not_provided": 3,
    "See_cases|Intellectual_disability|_X-linked_1": 1,
    "Severe_intellectual_deficiency|Autism": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_1|IQSEC2-related_disorder": 2,
    "Intellectual_disability|_X-linked_1|Intellectual_disability|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked_1|Intellectual_disability": 2,
    "Intellectual_disability|_X-linked_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked_1|not_specified|not_provided": 2,
    "Intellectual_disability|_X-linked_1|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "Intellectual_disability|_X-linked_1|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|IQSEC2-related_disorder|Intellectual_disability|_X-linked_1": 2,
    "not_provided|not_specified|Intellectual_disability|_X-linked_1": 2,
    "not_specified|Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_1": 1,
    "not_specified|Intellectual_disability|_X-linked_1|Inborn_genetic_diseases": 1,
    "IQSEC2-related_X-linked_neurodevelopmental_disorder": 1,
    "Intellectual_disability|_X-linked_1|Inborn_genetic_diseases|not_provided|Intellectual_disability": 1,
    "IQSEC2-related_disorder|not_provided|Intellectual_disability|_X-linked_1": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_1|Severe_intellectual_deficiency": 1,
    "not_provided|IQSEC2-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked_1": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_1|Tip-toe_gait": 1,
    "not_provided|Intellectual_disability|_X-linked_1|Tip-toe_gait": 1,
    "Intellectual_disability|_X-linked_1|not_specified|not_provided|IQSEC2-related_disorder": 1,
    "Specific_learning_disability": 1,
    "not_specified|not_provided|Intellectual_disability|_X-linked_1|Inborn_genetic_diseases": 1,
    "IQSEC2-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked_1|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|IQSEC2-related_disorder": 1,
    "IQSEC2-related_disorder|not_provided|Intellectual_disability|_X-linked_1|Inborn_genetic_diseases": 1,
    "IQSEC2-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_1|IQSEC2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked_1|IQSEC2-related_disorder|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked_1|not_specified": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome": 608,
    "not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome": 23,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided": 26,
    "not_specified|History_of_neurodevelopmental_disorder|De_Lange_syndrome": 1,
    "Inborn_genetic_diseases|Congenital_muscular_hypertrophy-cerebral_syndrome": 17,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Inborn_genetic_diseases": 7,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|SMC1A-related_disorder": 2,
    "SMC1A-related_disorder": 10,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_specified": 4,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 41,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome": 4,
    "not_specified|Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 1,
    "Inborn_genetic_diseases|not_specified|Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|not_provided": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Inborn_genetic_diseases|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome": 6,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 21,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|not_provided": 4,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Cognitive_impairment|Abnormal_corpus_callosum_morphology|Spastic_paraplegia|Polyneuropathy|Cerebellar_atrophy|Dysarthria|Pectus_excavatum|Pes_cavus|not_provided": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Wiedemann-Steiner_syndrome": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome": 2,
    "not_specified|Congenital_muscular_hypertrophy-cerebral_syndrome": 5,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided": 2,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome|Inborn_genetic_diseases": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Intellectual_disability": 1,
    "SMC1A-related_disorder|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome": 1,
    "SMC1A-related_disorder|Congenital_muscular_hypertrophy-cerebral_syndrome": 2,
    "Microcephaly|Congenital_muscular_hypertrophy-cerebral_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome|Inborn_genetic_diseases": 1,
    "De_Lange_syndrome|not_specified|Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Epileptic_encephalopathy": 1,
    "not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 2,
    "SMC1A-related_cohesinopathy": 1,
    "Cornelia_de_Lange_syndrome_1|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome": 1,
    "Global_developmental_delay|Abnormal_facial_shape": 1,
    "not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome|SMC1A-related_disorder": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Inborn_genetic_diseases|not_specified": 1,
    "SMC1A-related_cohesinopathy|not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome": 1,
    "not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 2,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Congenital_muscular_hypertrophy-cerebral_syndrome": 1,
    "not_provided|Congenital_muscular_hypertrophy-cerebral_syndrome|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Inborn_genetic_diseases|SMC1A-related_disorder": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_specified|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 1,
    "SMC1A-related_disorder|Congenital_muscular_hypertrophy-cerebral_syndrome|Hypertonia|Microcephaly|Progressive_sensorineural_hearing_impairment|Hirsutism|Abnormal_heart_valve_morphology|Global_developmental_delay": 1,
    "not_specified|Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects": 1,
    "Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|SMC1A-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_85|_with_or_without_midline_brain_defects|Congenital_muscular_hypertrophy-cerebral_syndrome|not_provided|not_specified|De_Lange_syndrome": 1,
    "HSD10_mitochondrial_disease": 20,
    "HSD10_mitochondrial_disease|not_provided": 1,
    "not_provided|HSD10_mitochondrial_disease": 3,
    "HSD17B10-related_disorder": 2,
    "not_provided|HSD10_mitochondrial_disease|Neurodevelopmental_delay|Inborn_genetic_diseases": 1,
    "HSD10_mitochondrial_disease|not_specified": 1,
    "HSD10_mitochondrial_disease|not_specified|not_provided": 1,
    "HSD10_mitochondrial_disease|not_provided|not_specified": 1,
    "not_specified|HSD17B10-related_disorder|not_provided": 1,
    "HSD17B10-related_disorder|not_provided": 1,
    "HSD10_mitochondrial_disease|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "HUWE1-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "not_provided|HUWE1-related_disorder": 14,
    "Abnormal_corpus_callosum_morphology|not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided|HUWE1-related_disorder": 1,
    "not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type": 16,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided": 27,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type": 128,
    "HUWE1-related_disorder": 42,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 27,
    "not_provided|Inborn_genetic_diseases|HUWE1-related_disorder": 1,
    "not_provided|Non-syndromic_X-linked_intellectual_disability|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type|Intellectual_disability|not_provided": 1,
    "HUWE1-related_disorder|Inborn_genetic_diseases|not_provided": 6,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided|not_specified": 1,
    "Trigonocephaly-short_stature-developmental_delay_syndrome": 1,
    "not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|HUWE1-related_disorder": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_syndromic|_Turner_type": 3,
    "Inborn_genetic_diseases|HUWE1-related_disorder|not_provided": 3,
    "HUWE1-related_disorder|not_provided": 4,
    "Inborn_genetic_diseases|HUWE1-related_disorder|not_specified|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|HUWE1-related_disorder": 2,
    "Inborn_genetic_diseases|Global_developmental_delay|not_provided": 1,
    "HUWE1-related_disorder|not_provided|Inborn_genetic_diseases": 3,
    "HUWE1-related_disorder|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type|Intellectual_disability|Neurodevelopmental_delay": 1,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type|Trigonocephaly-short_stature-developmental_delay_syndrome|not_provided": 1,
    "not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_specified": 1,
    "not_specified|HUWE1-related_disorder|Inborn_genetic_diseases": 1,
    "Blepharophimosis|Atrial_septal_defect|Ventricular_septal_defect|Abnormal_facial_shape|Hypothyroidism|Visual_impairment|Severe_global_developmental_delay|Excessive_wrinkled_skin": 1,
    "Inborn_genetic_diseases|HUWE1-related_disorder|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|HUWE1-related_disorder|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "HUWE1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|HUWE1-related_disorder": 1,
    "not_provided|not_specified|HUWE1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|HUWE1-related_disorder|Inborn_genetic_diseases": 2,
    "not_specified|not_provided|Inborn_genetic_diseases|HUWE1-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided": 1,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type|Intellectual_disability": 1,
    "not_specified|HUWE1-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_syndromic|_Turner_type|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided": 1,
    "HUWE1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "not_provided|Autism_spectrum_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "X-linked_intellectual_disability|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "not_specified|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_provided": 1,
    "HUWE1-related_disorder|not_provided|not_specified": 1,
    "Trigonocephaly-short_stature-developmental_delay_syndrome|Intellectual_disability|_X-linked_syndromic|_Turner_type": 1,
    "HUWE1-related_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked_syndromic|_Turner_type|not_specified|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Siderius_type": 36,
    "Syndromic_X-linked_intellectual_disability_Siderius_type|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|PHF8-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Syndromic_X-linked_intellectual_disability_Siderius_type|Intellectual_disability": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_Siderius_type": 2,
    "PHF8-related_disorder": 6,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Siderius_type": 1,
    "Syndromic_X-linked_intellectual_disability_Siderius_type|not_provided": 3,
    "PHF8-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Siderius_type|not_specified": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|PHF8-related_disorder": 1,
    "PHF8-related_disorder|not_provided": 1,
    "not_provided|PHF8-related_disorder": 1,
    "PHF8-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|PHF8-related_disorder": 1,
    "Prieto_syndrome": 6,
    "not_specified|Prieto_syndrome": 1,
    "Subglottic_stenosis|Intellectual_disability|_moderate|Abnormal_facial_shape|Motor_stereotypies|Delayed_speech_and_language_development|Autism|Congenital_laryngomalacia|Sleep_apnea|Retrognathia": 1,
    "WNK3-related_condition": 1,
    "not_specified|WNK3-related_condition": 1,
    "Prieto_syndrome|not_specified": 1,
    "Prieto_syndrome|Neurodevelopmental_disorder": 4,
    "TSR2-related_disorder|not_provided": 2,
    "not_specified|TSR2-related_disorder": 1,
    "Diamond-Blackfan_anemia_14_with_mandibulofacial_dysostosis|Diamond-Blackfan_anemia_15_with_mandibulofacial_dysostosis": 1,
    "not_provided|Diamond-Blackfan_anemia_14_with_mandibulofacial_dysostosis|TSR2-related_disorder": 1,
    "TSR2-related_disorder": 1,
    "not_specified|not_provided|Aarskog_syndrome": 2,
    "not_provided|Aarskog_syndrome": 10,
    "Aarskog_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "FGD1-related_disorder|Inborn_genetic_diseases|not_provided": 3,
    "Aarskog_syndrome": 56,
    "Aarskog_syndrome|FGD1-related_disorder": 1,
    "Aarskog_syndrome|not_provided": 5,
    "not_provided|not_specified|TSR2-related_disorder|Inborn_genetic_diseases": 1,
    "FGD1-related_disorder": 9,
    "FGD1-related_disorder|Inborn_genetic_diseases": 1,
    "FGD1-related_disorder|not_provided": 5,
    "not_provided|FGD1-related_disorder": 2,
    "not_provided|Inborn_genetic_diseases|Aarskog_syndrome": 1,
    "FGD1-related_disorder|Intellectual_disability|not_provided": 1,
    "FGD1-related_disorder|History_of_neurodevelopmental_disorder|not_provided|Syndromic_X-linked_intellectual_disability_Claes-Jensen_type": 1,
    "FGD1-related_disorder|Inborn_genetic_diseases|Aarskog_syndrome": 1,
    "Polyhydramnios": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Aarskog_syndrome": 1,
    "Inborn_genetic_diseases|FGD1-related_disorder": 1,
    "Russell-Silver_syndrome|FGD1-related_disorder|Inborn_genetic_diseases|not_provided|Aarskog_syndrome|Intellectual_disability": 1,
    "FGD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability": 1,
    "Aarskog_syndrome|not_provided|FGD1-related_disorder": 1,
    "not_provided|FGD1-related_disorder|Aarskog_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Aarskog_syndrome": 1,
    "not_provided|FGD1-related_disorder|not_specified": 1,
    "FGD1-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Aarskog_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|FGD1-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|FGD1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|FGD1-related_disorder": 1,
    "ITIH6-related_disorder": 16,
    "not_specified|ITIH6-related_disorder": 1,
    "ITIH6-related_disorder|not_specified": 1,
    "not_provided|Bartter_disease_type_5": 3,
    "Bartter_disease_type_5": 14,
    "MAGED2-related_disorder": 2,
    "Bartter_disease_type_5|not_provided": 3,
    "Inborn_genetic_diseases|MAGED2-related_disorder": 1,
    "MAGED2-related_disorder|not_provided": 3,
    "Bartter_disease_type_5|MAGED2-related_disorder|not_provided": 1,
    "not_provided|MAGED2-related_disorder": 1,
    "X-linked_sideroblastic_anemia_1|not_provided": 4,
    "not_provided|X-linked_sideroblastic_anemia_1": 10,
    "X-linked_sideroblastic_anemia_1": 29,
    "Developmental_and_epileptic_encephalopathy|_36|not_provided|X-linked_sideroblastic_anemia_1|X-linked_erythropoietic_protoporphyria": 1,
    "ALAS2-related_disorder|not_provided|X-linked_sideroblastic_anemia_1": 3,
    "not_provided|X-linked_erythropoietic_protoporphyria|See_cases": 1,
    "X-linked_erythropoietic_protoporphyria": 7,
    "ALAS2-related_disorder|not_provided": 1,
    "not_provided|ALAS2-related_disorder|not_specified|X-linked_sideroblastic_anemia_1": 1,
    "not_provided|ALAS2-related_disorder|X-linked_sideroblastic_anemia_1": 2,
    "X-linked_sideroblastic_anemia_1|X-linked_erythropoietic_protoporphyria|not_specified|not_provided": 1,
    "not_specified|not_provided|X-linked_sideroblastic_anemia_1": 3,
    "not_specified|not_provided|X-linked_sideroblastic_anemia_1|X-linked_erythropoietic_protoporphyria": 1,
    "X-linked_sideroblastic_anemia_1|ALAS2-related_disorder|not_provided": 1,
    "not_provided|not_specified|ALAS2-related_disorder|X-linked_sideroblastic_anemia_1": 1,
    "not_provided|ALAS2-related_disorder": 4,
    "Inborn_genetic_diseases|not_provided|X-linked_sideroblastic_anemia_1": 1,
    "X-linked_erythropoietic_protoporphyria|X-linked_sideroblastic_anemia_1": 1,
    "not_provided|not_specified|X-linked_sideroblastic_anemia_1": 4,
    "X-linked_erythropoietic_protoporphyria|not_provided": 1,
    "Sideroblastic_anemia_1|_late-onset": 1,
    "ALAS2-related_disorder|not_specified|not_provided": 1,
    "not_specified|X-linked_sideroblastic_anemia_1": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|X-linked_sideroblastic_anemia_1|X-linked_erythropoietic_protoporphyria": 1,
    "not_specified|X-linked_sideroblastic_anemia_1|not_provided": 1,
    "Sideroblastic_anemia_1|_late-onset|X-linked_sideroblastic_anemia_1": 1,
    "X-linked_sideroblastic_anemia_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "X-linked_sideroblastic_anemia_1|X-linked_erythropoietic_protoporphyria": 1,
    "ALAS2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "X-linked_sideroblastic_anemia_1|Inborn_genetic_diseases": 1,
    "ALAS2-related_disorder": 2,
    "not_specified|not_provided|ALAS2-related_disorder|X-linked_erythropoietic_protoporphyria": 1,
    "Sideroblastic_Anemia_and_Ataxia|not_provided": 2,
    "Amyotrophic_Lateral_Sclerosis|_Dominant|Amyotrophic_lateral_sclerosis_type_15": 2,
    "Amyotrophic_lateral_sclerosis_type_15": 128,
    "not_provided|Amyotrophic_lateral_sclerosis_type_15|Amyotrophic_Lateral_Sclerosis|_Dominant": 2,
    "Amyotrophic_lateral_sclerosis_type_15|not_provided": 5,
    "UBQLN2-related_disorder|Amyotrophic_lateral_sclerosis_type_15": 2,
    "UBQLN2-related_disorder": 11,
    "UBQLN2-related_disorder|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_15|Amyotrophic_Lateral_Sclerosis|_Dominant": 5,
    "not_provided|Amyotrophic_lateral_sclerosis_type_15": 5,
    "not_specified|Amyotrophic_lateral_sclerosis_type_15": 4,
    "Amyotrophic_lateral_sclerosis_type_15|not_specified": 2,
    "Amyotrophic_lateral_sclerosis_type_15|UBQLN2-related_disorder|not_provided": 3,
    "UBQLN2-related_disorder|Amyotrophic_lateral_sclerosis_type_15|not_provided": 1,
    "Amyotrophic_lateral_sclerosis_type_15|UBQLN2-related_disorder": 2,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_15": 1,
    "not_provided|not_specified|Amyotrophic_lateral_sclerosis_type_15|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "not_specified|not_provided|Amyotrophic_lateral_sclerosis_type_15|Amyotrophic_Lateral_Sclerosis|_Dominant": 1,
    "not_specified|Amyotrophic_lateral_sclerosis_type_15|UBQLN2-related_disorder": 1,
    "Amyotrophic_lateral_sclerosis_type_15|not_provided|UBQLN2-related_disorder|Amyotrophic_lateral_sclerosis": 1,
    "FAAH2-related_disorder": 13,
    "Lui-Jee-Baron_syndrome": 2,
    "Developmental_and_epileptic_encephalopathy|_8": 272,
    "ARHGEF9-related_disorder|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_8": 20,
    "not_specified|Developmental_and_epileptic_encephalopathy|_8|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_8": 8,
    "Developmental_and_epileptic_encephalopathy|_8|not_specified": 7,
    "Developmental_and_epileptic_encephalopathy|_8|not_provided": 10,
    "not_specified|Developmental_and_epileptic_encephalopathy|_8": 8,
    "Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases": 9,
    "Developmental_and_epileptic_encephalopathy|_8|Autism_spectrum_disorder|not_provided": 1,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases": 1,
    "ARHGEF9-related_disorder|Developmental_and_epileptic_encephalopathy|_8": 1,
    "Developmental_and_epileptic_encephalopathy|_8|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_8|Seizure": 1,
    "Developmental_disorder|Developmental_and_epileptic_encephalopathy|_8": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_8|ARHGEF9-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_8|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_8|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_8": 1,
    "Inborn_genetic_diseases|ARHGEF9-related_disorder|Developmental_and_epileptic_encephalopathy|_8|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|ARHGEF9-related_disorder|Developmental_and_epileptic_encephalopathy|_8": 1,
    "Autism_spectrum_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_8": 1,
    "not_provided|Global_developmental_delay|Developmental_and_epileptic_encephalopathy|_8": 1,
    "Developmental_and_epileptic_encephalopathy|_8|ARHGEF9-related_disorder|not_specified": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_8|ARHGEF9-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_8|not_provided|not_specified": 2,
    "not_provided|ARHGEF9-related_disorder|Developmental_and_epileptic_encephalopathy|_8": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_8|ARHGEF9-related_neurodevelopmental_disorder|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_8|ARHGEF9-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_8|Microcephaly": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_8": 1,
    "ARHGEF9-related_disorder|Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_8|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_8|not_provided|Autism": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_8": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_8|Inborn_genetic_diseases": 1,
    "Epilepsy|Developmental_and_epileptic_encephalopathy|_8": 1,
    "Developmental_and_epileptic_encephalopathy|_8|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "ARHGEF9-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_8|not_provided|ARHGEF9-related_disorder": 1,
    "AMER1-related_disorder|Osteopathia_striata_with_cranial_sclerosis|not_provided": 1,
    "Osteopathia_striata_with_cranial_sclerosis": 35,
    "not_provided|Inborn_genetic_diseases|Osteopathia_striata_with_cranial_sclerosis": 1,
    "not_provided|AMER1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|AMER1-related_disorder|not_provided": 1,
    "AMER1-related_disorder": 12,
    "Osteopathia_striata_with_cranial_sclerosis|Inborn_genetic_diseases|not_provided": 1,
    "AMER1-related_disorder|not_provided": 5,
    "not_provided|AMER1-related_disorder": 3,
    "not_provided|Osteopathia_striata_with_cranial_sclerosis|Inborn_genetic_diseases": 1,
    "Myocarditis|Febrile_seizure_(within_the_age_range_of_3_months_to_6_years)|Macrocephaly|Ventriculomegaly": 1,
    "not_provided|Osteopathia_striata_with_cranial_sclerosis": 6,
    "AMER1-related_disorder|Inborn_genetic_diseases": 1,
    "AMER1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Osteopathia_striata_with_cranial_sclerosis|not_provided": 2,
    "AMER1-related_disorder|not_specified|not_provided|Osteopathia_striata_with_cranial_sclerosis|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Obesity": 1,
    "Osteopathia_striata_with_cranial_sclerosis|not_provided|Inborn_genetic_diseases": 1,
    "AMER1-related_disorder|not_provided|Osteopathia_striata_with_cranial_sclerosis|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Osteopathia_striata_with_cranial_sclerosis|not_provided": 1,
    "not_provided|Spinocerebellar_ataxia|_X-linked": 1,
    "AMER1-related_disorder|not_provided|Inborn_genetic_diseases|Osteopathia_striata_with_cranial_sclerosis": 1,
    "not_provided|AMER1-related_disorder|Osteopathia_striata_with_cranial_sclerosis": 1,
    "Osteopathia_striata_with_cranial_sclerosis|not_provided|not_specified": 1,
    "MTMR8-related_disorder": 11,
    "Genetic_developmental_and_epileptic_encephalopathy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Wieacker-Wolff_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Wieacker-Wolff_syndrome|ZC4H2-related_disorder": 1,
    "Wieacker-Wolff_syndrome|_female-restricted|not_provided": 1,
    "Wieacker-Wolff_syndrome|_female-restricted": 15,
    "Neurodevelopmental_disorder|Wieacker-Wolff_syndrome": 1,
    "Wieacker-Wolff_syndrome|Wieacker-Wolff_syndrome|_female-restricted|not_provided": 1,
    "Wieacker-Wolff_syndrome|_female-restricted|Wieacker-Wolff_syndrome|not_provided": 1,
    "not_provided|ZC4H2-related_disorder|Inborn_genetic_diseases": 1,
    "Wieacker-Wolff_syndrome|Wieacker-Wolff_syndrome|_female-restricted": 2,
    "Wieacker-Wolff_syndrome|not_provided": 4,
    "not_provided|ZC4H2-related_disorder": 1,
    "Inborn_genetic_diseases|Wieacker-Wolff_syndrome|_female-restricted|Wieacker-Wolff_syndrome|not_provided": 1,
    "ZC4H2-related_X-linked_intellectual_disability|not_provided": 1,
    "not_provided|Wieacker-Wolff_syndrome": 2,
    "Wieacker-Wolff_syndrome|_female-restricted|Inborn_genetic_diseases": 1,
    "Wieacker-Wolff_syndrome|not_provided|ZC4H2-related_X-linked_intellectual_disability": 1,
    "ZC4H2-related_disorder|Inborn_genetic_diseases": 1,
    "Wieacker-Wolff_syndrome|_female-restricted|not_provided|Inborn_genetic_diseases|Wieacker-Wolff_syndrome": 1,
    "Wieacker-Wolff_syndrome_(spectrum)": 1,
    "Wilson-Turner_syndrome": 83,
    "Wilson-Turner_syndrome|not_provided": 15,
    "not_provided|Wilson-Turner_syndrome": 6,
    "not_specified|Wilson-Turner_syndrome": 5,
    "See_cases|not_specified|not_provided|Wilson-Turner_syndrome": 1,
    "Wilson-Turner_syndrome|not_specified": 4,
    "Wilson-Turner_syndrome|LAS1L-related_disorder": 1,
    "Intellectual_disability|Wilson-Turner_syndrome|not_provided": 1,
    "Wilson-Turner_syndrome|Global_developmental_delay": 1,
    "LAS1L-related_disorder|Wilson-Turner_syndrome": 2,
    "not_provided|LAS1L-related_disorder": 1,
    "LAS1L-related_disorder": 2,
    "not_provided|MSN-related_disorder": 2,
    "MSN-related_disorder": 1,
    "not_provided|Combined_immunodeficiency_due_to_moesin_deficiency": 1,
    "MSN-related_disorder|not_provided": 2,
    "Combined_immunodeficiency_due_to_moesin_deficiency": 4,
    "Combined_immunodeficiency_due_to_moesin_deficiency|not_provided": 2,
    "MSN-related_disorder|Combined_immunodeficiency_due_to_moesin_deficiency": 1,
    "not_provided|MSN-related_disorder|Inborn_genetic_diseases": 1,
    "VSIG4-related_disorder": 12,
    "VSIG4-related_disorder|not_specified|not_provided": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia": 432,
    "AR-related_disorder": 15,
    "Androgen_resistance_syndrome|Kennedy_disease": 362,
    "Androgen_resistance_syndrome": 96,
    "Partial_androgen_insensitivity_syndrome": 15,
    "Androgen_resistance_syndrome|Prostate_cancer|Hypospadias_1|_X-linked|Kennedy_disease|Partial_androgen_insensitivity_syndrome|Ovarian_cancer": 1,
    "Kennedy_disease|Androgen_resistance_syndrome": 124,
    "Kennedy_disease|Androgen_resistance_syndrome|Partial_androgen_insensitivity_syndrome|Hypospadias_1|_X-linked|Familial_prostate_cancer": 1,
    "Androgen_resistance_syndrome|Prostate_cancer|Kennedy_disease|Inborn_genetic_diseases": 1,
    "AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease|not_provided": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_specified|AR-related_disorder|not_provided|Ovarian_cancer": 1,
    "not_provided|Androgen_resistance_syndrome|Kennedy_disease|not_specified": 2,
    "not_provided|Kennedy_disease|Androgen_resistance_syndrome|not_specified|Partial_androgen_insensitivity_syndrome": 1,
    "AR-related_disorder|not_specified|not_provided|Androgen_resistance_syndrome|Kennedy_disease": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_specified|not_provided": 6,
    "not_specified|not_provided|AR-related_disorder": 1,
    "not_provided|Kennedy_disease|Androgen_resistance_syndrome|AR-related_disorder": 1,
    "not_specified|Androgen_resistance_syndrome|Kennedy_disease": 3,
    "Androgen_resistance_syndrome|Kennedy_disease|Inborn_genetic_diseases|not_provided|Partial_androgen_insensitivity_syndrome|Prostate_cancer|Hypospadias_1|_X-linked": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_provided": 18,
    "AR-related_disorder|not_provided": 3,
    "not_provided|Kennedy_disease|Partial_androgen_insensitivity_syndrome|Prostate_cancer|Androgen_resistance_syndrome|Hypospadias_1|_X-linked": 1,
    "Kennedy_disease|AR-related_disorder|Partial_androgen_insensitivity_syndrome|Prostate_cancer|Androgen_resistance_syndrome|Hypospadias_1|_X-linked": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_specified|Hypospadias_1|_X-linked|Partial_androgen_insensitivity_syndrome|Prostate_cancer|not_provided": 1,
    "Kennedy_disease|not_specified|Androgen_resistance_syndrome|not_provided": 1,
    "not_provided|Kennedy_disease|Androgen_resistance_syndrome|not_specified": 1,
    "not_provided|Androgen_resistance_syndrome|Kennedy_disease|not_specified|Hypospadias_1|_X-linked|Partial_androgen_insensitivity_syndrome|Prostate_cancer": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_provided|not_specified": 2,
    "not_specified|not_provided|Androgen_resistance_syndrome|Kennedy_disease": 2,
    "Partial_androgen_insensitivity_syndrome|Prostate_cancer|Kennedy_disease|Hypospadias_1|_X-linked|Androgen_resistance_syndrome|AR-related_disorder|not_provided|not_specified": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_provided|AR-related_disorder": 1,
    "AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease": 6,
    "Partial_androgen_insensitivity_syndrome|Posterior_hypospadias|Kennedy_disease|Androgen_resistance_syndrome|Hypospadias_1|_X-linked|Familial_prostate_cancer|not_provided|Male_infertility|Prostate_cancer|not_specified": 1,
    "not_provided|Androgen_resistance_syndrome": 5,
    "not_provided|Androgen_resistance_syndrome|Kennedy_disease|Prostate_cancer": 1,
    "Aplasia_of_the_uterus|Female_external_genitalia_in_individual_with_46|XY_karyotype|Absent_pubic_hair|Absent_axillary_hair": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_specified": 2,
    "not_provided|not_specified|Androgen_resistance_syndrome|Kennedy_disease": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|AR-related_disorder|not_specified|Male_infertility": 1,
    "AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease|Hypospadias_1|_X-linked|Prostate_cancer|Partial_androgen_insensitivity_syndrome|not_provided": 1,
    "Hypospadias_1|_X-linked|Kennedy_disease|Prostate_cancer|_hereditary|_X-linked_3|Partial_androgen_insensitivity_syndrome|Androgen_resistance_syndrome": 1,
    "Kennedy_disease|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Kennedy_disease|Androgen_resistance_syndrome|not_provided": 1,
    "Kennedy_disease": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Inborn_genetic_diseases": 3,
    "Androgen_resistance_syndrome|Kennedy_disease|not_provided|Male_infertility": 1,
    "not_provided|Kennedy_disease|Androgen_resistance_syndrome": 9,
    "not_specified|Androgen_resistance_syndrome|Kennedy_disease|AR-related_disorder": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Prostate_cancer": 2,
    "Complete_androgen_insensitivity_syndrome": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "not_provided|AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease|not_specified": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Partial_androgen_insensitivity_syndrome|Hypospadias_1|_X-linked|Prostate_cancer": 1,
    "Androgen_resistance_syndrome|Partial_androgen_insensitivity_syndrome|AR-related_disorder|Kennedy_disease|not_specified|not_provided|Hypospadias_1|_X-linked": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|Ovarian_cancer": 2,
    "Inborn_genetic_diseases|Male_infertility": 1,
    "Inborn_genetic_diseases|not_provided|Androgen_resistance_syndrome|Kennedy_disease": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Non-obstructive_azoospermia|Male_infertility|Prostate_cancer": 1,
    "not_provided|AR-related_disorder": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Partial_androgen_insensitivity_syndrome|not_specified|not_provided": 1,
    "Androgen_resistance_syndrome|Hypospadias_1|_X-linked|Prostate_cancer|Kennedy_disease|Partial_androgen_insensitivity_syndrome|AR-related_disorder|not_specified|not_provided": 1,
    "AR-related_disorder|Androgen_resistance_syndrome|not_provided": 1,
    "not_specified|not_provided|AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease": 2,
    "Androgen_resistance_syndrome|AR-related_disorder": 2,
    "Androgen_resistance_syndrome|Hypospadias_1|_X-linked|Androgen_insensitivity|_partial|_with_breast_cancer|AR-related_disorder": 1,
    "not_provided|Androgen_resistance_syndrome|Kennedy_disease": 13,
    "AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease|Male_infertility|Hypospadias_1|_X-linked|Partial_androgen_insensitivity_syndrome|Prostate_cancer|_hereditary|_X-linked_3|not_provided|not_specified": 1,
    "Pure_gonadal_dysgenesis_46|XY|not_provided": 1,
    "Male_infertility|Androgen_resistance_syndrome": 1,
    "AR-related_disorder|Androgen_resistance_syndrome|Kennedy_disease|Inborn_genetic_diseases|not_provided": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|Prostate_cancer|_hereditary|_X-linked_3": 1,
    "not_specified|Hypospadias_1|_X-linked": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|AR-related_disorder": 2,
    "not_specified|not_provided|Androgen_resistance_syndrome|Kennedy_disease|Male_infertility|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation": 1,
    "Androgen_resistance_syndrome|not_provided": 4,
    "Partial_androgen_insensitivity_syndrome|Androgen_resistance_syndrome|not_provided": 1,
    "not_provided|Partial_androgen_insensitivity_syndrome": 2,
    "Disorder_of_sexual_differentiation|Androgen_resistance_syndrome|Kennedy_disease|not_provided|Partial_androgen_insensitivity_syndrome": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|Prostate_cancer|Non-obstructive_azoospermia|Male_infertility": 1,
    "Partial_androgen_insensitivity_syndrome|Kennedy_disease|Androgen_resistance_syndrome|not_provided": 1,
    "Androgen_insensitivity|_partial|_with_breast_cancer": 1,
    "Partial_androgen_insensitivity_syndrome|not_provided|Kennedy_disease|Androgen_resistance_syndrome": 1,
    "Androgen_resistance_syndrome|not_specified|not_provided": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|AR-related_disorder|Castleman-Kojima_disease|not_specified|not_provided|Male_infertility|Partial_androgen_insensitivity_syndrome": 1,
    "not_specified|Kennedy_disease|Androgen_resistance_syndrome": 1,
    "Inborn_genetic_diseases|Kennedy_disease|Androgen_resistance_syndrome": 1,
    "Partial_androgen_insensitivity_syndrome|Kennedy_disease|Androgen_resistance_syndrome": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|not_provided": 4,
    "Androgen_resistance_syndrome|Inborn_genetic_diseases|Kennedy_disease|not_provided": 1,
    "Prostate_cancer|_somatic|Kennedy_disease|Androgen_resistance_syndrome|not_specified": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|Prostate_cancer_susceptibility|Prostate_cancer": 1,
    "Prostate_cancer|_somatic|Prostate_cancer|Kennedy_disease|Androgen_resistance_syndrome": 1,
    "Partial_androgen_insensitivity_syndrome|Androgen_resistance_syndrome|Kennedy_disease": 2,
    "Androgen_resistance_syndrome|Male_infertility|not_provided|Kennedy_disease|Prostate_cancer|_hereditary|_X-linked_3|Hypospadias_1|_X-linked|Partial_androgen_insensitivity_syndrome": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|not_specified|not_provided|Male_infertility|Partial_androgen_insensitivity_syndrome|Prostate_cancer": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|not_provided|Partial_androgen_insensitivity_syndrome": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|AR-related_disorder": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|AR-related_disorder|Male_infertility": 1,
    "Non-obstructive_azoospermia|Male_infertility": 1,
    "Androgen_resistance_syndrome|not_provided|Kennedy_disease": 3,
    "Partial_androgen_insensitivity_syndrome|not_provided|Androgen_resistance_syndrome|Kennedy_disease": 1,
    "Androgen_resistance_syndrome|Kennedy_disease|not_provided|Partial_androgen_insensitivity_syndrome": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|Male_infertility|Partial_androgen_insensitivity_syndrome": 1,
    "Kennedy_disease|Androgen_resistance_syndrome|AR-related_disorder|Hypospadias_1|_X-linked|Prostate_cancer|Partial_androgen_insensitivity_syndrome": 1,
    "Androgen_resistance_syndrome|Hypospadias_1|_X-linked|not_provided|Kennedy_disease": 1,
    "not_specified|not_provided|Kennedy_disease|Androgen_resistance_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|OPHN1-related_disorder": 2,
    "not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|OPHN1-related_disorder|not_specified|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 1,
    "X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 56,
    "X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|not_provided": 6,
    "OPHN1-related_disorder": 8,
    "not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|OPHN1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Genetic_developmental_and_epileptic_encephalopathy|not_provided": 1,
    "OPHN1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|not_specified|OPHN1-related_disorder|not_provided": 2,
    "not_specified|not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|OPHN1-related_disorder|not_specified|not_provided|See_cases": 1,
    "X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 4,
    "not_specified|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|Inborn_genetic_diseases": 1,
    "OPHN1-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|OPHN1-related_disorder": 2,
    "OPHN1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 1,
    "not_specified|not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 1,
    "Congenital_cerebellar_hypoplasia|Hypoplasia_of_the_corpus_callosum|Delayed_gross_motor_development|Seizure|Nystagmus|Oligohydramnios": 1,
    "X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|not_provided|not_specified": 1,
    "not_provided|not_specified|OPHN1-related_disorder": 1,
    "not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome|Abnormality_of_the_nervous_system": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|X-linked_intellectual_disability-cerebellar_hypoplasia_syndrome": 1,
    "EFNB1-related_disorder": 7,
    "Craniofrontonasal_syndrome": 34,
    "not_provided|Craniofrontonasal_syndrome": 11,
    "Craniofrontonasal_syndrome|not_provided": 1,
    "not_provided|EFNB1-related_disorder": 1,
    "not_specified|not_provided|Craniofrontonasal_syndrome": 1,
    "PJA1-related_disorder": 1,
    "PJA1-related_disorder|not_provided": 1,
    "not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia|Tooth_agenesis|_selective|_X-linked|_1": 3,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided": 12,
    "EDA-related_disorder": 11,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|EDA-related_disorder": 2,
    "Tooth_agenesis|_selective|_X-linked|_1|Hypohidrotic_X-linked_ectodermal_dysplasia": 2,
    "Anhidrotic_ectodermal_dysplasia|Hypohidrotic_X-linked_ectodermal_dysplasia": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|Tooth_agenesis|_selective|_X-linked|_1": 5,
    "not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia": 13,
    "EDA-related_disorder|not_specified|not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|Tooth_agenesis|_selective|_X-linked|_1": 1,
    "not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia|not_specified": 1,
    "not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia|Anhidrotic_ectodermal_dysplasia": 1,
    "not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia|EDA-related_disorder": 2,
    "Tooth_agenesis|_selective|_X-linked|_1|Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|Ectodermal_dysplasia": 1,
    "not_specified|Hypohidrotic_X-linked_ectodermal_dysplasia": 3,
    "not_provided|EDA-related_disorder|Hypohidrotic_X-linked_ectodermal_dysplasia|Tooth_agenesis|_selective|_X-linked|_1": 1,
    "EDA-related_disorder|Hypohidrotic_X-linked_ectodermal_dysplasia": 2,
    "Tooth_agenesis|_selective|_X-linked|_1|not_provided|Hypohidrotic_X-linked_ectodermal_dysplasia": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_specified": 1,
    "not_provided|EDA-related_disorder|Hypohidrotic_X-linked_ectodermal_dysplasia": 1,
    "Anhidrotic_ectodermal_dysplasia|Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided": 1,
    "not_provided|not_specified|Hypohidrotic_X-linked_ectodermal_dysplasia": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|EDA-related_disorder": 1,
    "Inborn_genetic_diseases|Hypohidrotic_X-linked_ectodermal_dysplasia": 2,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|not_specified": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|Asphyxiating_thoracic_dystrophy_3": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|Ectodermal_dysplasia": 1,
    "Hypodontia|Hypohidrotic_X-linked_ectodermal_dysplasia|Tooth_agenesis|_selective|_X-linked|_1|not_provided|Anhidrotic_ectodermal_dysplasia|Ectodermal_dysplasia": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|Anhidrotic_ectodermal_dysplasia": 1,
    "Tooth_agenesis|_selective|_X-linked|_1|Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|Inborn_genetic_diseases": 1,
    "EDA-related_disorder|Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|Tooth_agenesis|_selective|_X-linked|_1|See_cases|not_provided": 1,
    "Hypohidrotic_X-linked_ectodermal_dysplasia|EDA-related_disorder|See_cases|not_provided": 1,
    "Inborn_genetic_diseases|Tooth_agenesis|_selective|_X-linked|_1|Hypohidrotic_X-linked_ectodermal_dysplasia|not_provided|Hypodontia|EDA-related_disorder": 1,
    "Corpus_callosum_agenesis-intellectual_disability-coloboma-micrognathia_syndrome": 4,
    "IGBP1-related_disorder": 2,
    "not_specified|IGBP1-related_disorder|not_provided": 1,
    "not_provided|IGBP1-related_disorder": 1,
    "not_specified|Corpus_callosum_agenesis-intellectual_disability-coloboma-micrognathia_syndrome": 1,
    "DGAT2L6-related_disorder": 6,
    "DGAT2L6-related_disorder|not_provided": 1,
    "ARR3-related_disorder": 5,
    "not_provided|ARR3-related_disorder": 1,
    "Myopia_26|_X-linked|_female-limited|ARR3-related_disorder": 1,
    "Myopia_26|_X-linked|_female-limited": 5,
    "Inborn_genetic_diseases|Myopia_26|_X-linked|_female-limited": 1,
    "Intellectual_disability|_X-linked_100|not_provided": 6,
    "KIF4A-related_disorder|not_provided": 2,
    "Intellectual_disability|_X-linked_100": 17,
    "Congenital_cerebellar_hypoplasia|Ventriculomegaly|Corpus_callosum|_agenesis_of|Intellectual_disability|_X-linked_100|Hydrocephalus|Multicystic_kidney_dysplasia": 1,
    "KIF4A-related_disorder|not_specified": 1,
    "Taurodontism|_microdontia|_and_dens_invaginatus": 2,
    "Intellectual_disability|_X-linked_100|KIF4A-related_disorder|not_provided": 1,
    "KIF4A-related_disorder": 10,
    "not_provided|KIF4A-related_disorder": 2,
    "Poor_motor_coordination|Difficulty_walking|Generalized_hypotonia|Horizontal_nystagmus|Gynecomastia|Pes_planus|Sleep_abnormality|Obesity|Delayed_speech_and_language_development|Hypotonia": 1,
    "not_provided|Intellectual_disability|_X-linked_100": 2,
    "KIF4A-related_disorder|Intellectual_disability|_X-linked_100": 1,
    "not_specified|KIF4A-related_disorder": 2,
    "not_provided|KIF4A-related_disorder|not_specified": 1,
    "KIF4A-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked_90": 45,
    "not_provided|Intellectual_disability|_X-linked_90|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_90|Inborn_genetic_diseases": 2,
    "Intellectual_disability|_X-linked_90|not_provided": 5,
    "not_provided|Intellectual_disability|_X-linked_90": 4,
    "Inborn_genetic_diseases|not_provided|not_specified|Intellectual_disability|_X-linked_90": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|DLG3-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|DLG3-related_disorder": 1,
    "Intellectual_disability|_X-linked_90|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_90": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|DLG3-related_disorder": 1,
    "DLG3-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_X-linked_90": 1,
    "DLG3-related_disorder|not_provided|Inborn_genetic_diseases": 2,
    "DLG3-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_90|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|DLG3-related_disorder": 1,
    "TEX11-related_disorder": 7,
    "not_specified|not_provided|TEX11-related_disorder": 1,
    "not_specified|Spermatogenic_failure|_X-linked|_2|not_provided": 1,
    "TEX11-related_disorder|not_provided": 1,
    "not_specified|not_provided|Spermatogenic_failure|_X-linked|_2": 1,
    "not_provided|TEX11-related_disorder": 1,
    "TEX11-related_disorder|Spermatogenic_failure|_X-linked|_2|not_provided": 1,
    "not_specified|SLC7A3-related_disorder": 1,
    "SLC7A3-related_disorder|not_provided": 1,
    "SLC7A3-related_disorder": 8,
    "Clinodactyly|Intellectual_disability|_moderate|Abnormality_of_the_face|Macrocephaly|Short_5th_metacarpal": 2,
    "X-linked_severe_combined_immunodeficiency": 374,
    "X-linked_severe_combined_immunodeficiency|IL2RG-related_disorder": 1,
    "not_provided|X-linked_severe_combined_immunodeficiency": 13,
    "X-linked_severe_combined_immunodeficiency|not_provided": 17,
    "X-linked_severe_combined_immunodeficiency|Inborn_genetic_diseases": 6,
    "X-linked_severe_combined_immunodeficiency|Combined_immunodeficiency|_X-linked": 8,
    "Inborn_genetic_diseases|X-linked_severe_combined_immunodeficiency": 5,
    "X-linked_severe_combined_immunodeficiency|Combined_immunodeficiency|_X-linked|not_provided": 2,
    "X-linked_severe_combined_immunodeficiency|IL2RG-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|X-linked_severe_combined_immunodeficiency": 5,
    "not_provided|X-linked_severe_combined_immunodeficiency|Combined_immunodeficiency|_X-linked": 2,
    "Inborn_genetic_diseases|X-linked_severe_combined_immunodeficiency|Combined_immunodeficiency|_X-linked": 1,
    "not_specified|not_provided|X-linked_severe_combined_immunodeficiency": 2,
    "Combined_immunodeficiency|_X-linked|X-linked_severe_combined_immunodeficiency": 2,
    "Combined_immunodeficiency|_X-linked": 3,
    "not_provided|Inborn_genetic_diseases|X-linked_severe_combined_immunodeficiency": 1,
    "not_specified|Combined_immunodeficiency|_X-linked|X-linked_severe_combined_immunodeficiency": 1,
    "IL2RG-related_disorder|X-linked_severe_combined_immunodeficiency": 2,
    "IL2RG-related_disorder|Inborn_genetic_diseases|X-linked_severe_combined_immunodeficiency": 1,
    "Inborn_genetic_diseases|IL2RG-related_disorder|X-linked_severe_combined_immunodeficiency": 1,
    "IL2RG-related_disorder": 1,
    "IL2RG-related_disorder|X-linked_severe_combined_immunodeficiency|not_provided": 1,
    "Inborn_genetic_diseases|X-linked_severe_combined_immunodeficiency|IL2RG-related_disorder": 1,
    "MED12-related_disorder": 19,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 92,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 4,
    "FG_syndrome|not_specified": 20,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 82,
    "not_provided|FG_syndrome": 49,
    "not_specified|FG_syndrome": 21,
    "Angiosarcoma|Uterine_leiomyoma": 1,
    "Nephroblastoma|Uterine_leiomyoma": 1,
    "FG_syndrome|not_specified|MED12-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome|Neurodevelopmental_disorder|Syndromic_intellectual_disability|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 17,
    "FG_syndrome|not_provided": 45,
    "not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_specified|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "FG_syndrome_1": 24,
    "MED12-related_intellectual_disability_syndrome|FG_syndrome": 1,
    "not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome": 1,
    "FG_syndrome|MED12-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|MED12-related_disorder|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "not_provided|FG_syndrome_1|MED12-related_intellectual_disability_syndrome|FG_syndrome": 1,
    "FG_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "not_provided|MED12-related_disorder|FG_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "FG_syndrome_1|MED12-related_intellectual_disability_syndrome": 1,
    "FG_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome": 1,
    "MED12-related_disorder|FG_syndrome": 3,
    "X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_provided|FG_syndrome": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|FG_syndrome": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|not_provided": 1,
    "FG_syndrome|MED12-related_disorder|not_specified": 2,
    "MED12-related_disorder|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|not_provided": 13,
    "FG_syndrome|MED12-related_disorder": 10,
    "FG_syndrome|MED12-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|not_specified|not_provided|FG_syndrome": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 12,
    "FG_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 13,
    "not_provided|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome_1": 1,
    "Inborn_genetic_diseases|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome|not_provided|FG_syndrome_1": 1,
    "FG_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus": 6,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome": 13,
    "X-linked_intellectual_disability_with_marfanoid_habitus|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome": 1,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MED12-related_disorder": 3,
    "not_provided|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 13,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 9,
    "FG_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|FG_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome_1|not_provided": 5,
    "Dilated_cardiomyopathy_1Y|FG_syndrome": 1,
    "not_provided|FG_syndrome|FG_syndrome_1": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|not_provided|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MED12-related_disorder": 2,
    "FG_syndrome|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1": 1,
    "FG_syndrome|not_provided|not_specified": 1,
    "FG_syndrome|FG_syndrome_1": 1,
    "FG_syndrome_1|FG_syndrome|not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "X-linked_MED12-related_disorder|not_provided|FG_syndrome": 1,
    "MED12-related_disorder|not_provided|not_specified": 1,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "not_provided|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome": 8,
    "FG_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus": 3,
    "FG_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|FG_syndrome_1": 4,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome": 1,
    "not_provided|MED12-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|not_provided": 1,
    "Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "MED12-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome": 1,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome|not_specified": 1,
    "FG_syndrome|Cardiovascular_phenotype": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_1|not_provided|FG_syndrome": 2,
    "FG_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MED12-related_disorder": 2,
    "not_specified|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_provided|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 2,
    "FG_syndrome|not_provided|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1": 3,
    "FG_syndrome_1|not_provided|FG_syndrome": 1,
    "FG_syndrome|not_provided|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_1": 1,
    "MED12-related_disorder|FG_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Intellectual_disability|Imperforate_anus|Abnormal_facial_shape|Corpus_callosum|_agenesis_of|Broad_thumb|Global_developmental_delay": 1,
    "FG_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 4,
    "Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|not_provided": 1,
    "not_specified|not_provided|FG_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|MED12-related_disorder": 1,
    "FG_syndrome|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|not_provided": 1,
    "not_provided|FG_syndrome|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome": 2,
    "not_provided|MED12-related_intellectual_disability_syndrome|FG_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome|MED12-related_disorder": 1,
    "not_provided|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_specified": 1,
    "MED12-related_disorder|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|MED12-related_disorder|MED12-related_intellectual_disability_syndrome|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "FG_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_provided|FG_syndrome_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Intellectual_disability": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|See_cases": 1,
    "MED12-related_intellectual_disability_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Nonspecific_Intellectual_Disability": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|MED12-related_disorder": 1,
    "FG_syndrome|not_provided|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "MED12-related_disorder|FG_syndrome|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|not_specified": 1,
    "not_provided|FG_syndrome|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|FG_syndrome_1|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|MED12-related_disorder|not_provided": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|not_specified|not_provided|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|FG_syndrome": 1,
    "FG_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "not_provided|X-linked_intellectual_disability_with_marfanoid_habitus|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome|MED12-related_intellectual_disability_syndrome|not_provided": 1,
    "FG_syndrome_1|FG_syndrome|MED12-related_disorder|not_provided": 1,
    "MED12-related_disorder|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Inborn_genetic_diseases|FG_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_provided|FG_syndrome_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FG_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "See_cases|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "Global_developmental_delay|Abnormal_facial_shape|Absent_speech|Expressive_language_delay|Seizure|Microcephaly|Ventriculomegaly": 1,
    "FG_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1": 1,
    "not_specified|not_provided|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "MED12-related_disorder|not_specified": 1,
    "MED12-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "not_provided|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "MED12-related_disorder|Nonspecific_Intellectual_Disability|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome": 1,
    "not_provided|Intellectual_disability|FG_syndrome": 1,
    "MED12-related_intellectual_disability_syndrome": 3,
    "See_cases|FG_syndrome_1": 1,
    "MED12-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MED12-related_disorder|FG_syndrome": 1,
    "MED12-related_neurodevelopmental_delay": 1,
    "FG_syndrome|not_provided|FG_syndrome_1": 1,
    "Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|not_provided": 2,
    "X-linked_MED12-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_1|Intellectual_disability": 1,
    "FG_syndrome|FG_syndrome_1|not_provided": 1,
    "Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome_1": 4,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|MED12-related_disorder": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|not_provided|FG_syndrome": 1,
    "Intellectual_disability|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MED12-related_disorder|not_provided|FG_syndrome": 1,
    "FG_syndrome|Intellectual_disability|not_provided|not_specified": 1,
    "not_specified|FG_syndrome|MED12-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|MED12-related_disorder|FG_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ehlers-Danlos_syndrome|_classic_type|FG_syndrome|not_specified": 1,
    "MED12-related_disorder|FG_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome|not_provided|MED12-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|not_specified|not_provided": 1,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|MED12-related_disorder|not_provided": 1,
    "MED12-related_disorder|FG_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome|not_specified|not_provided|Intellectual_disability": 1,
    "not_provided|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|FG_syndrome_1|X-linked_intellectual_disability_with_marfanoid_habitus|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome": 1,
    "MED12-related_intellectual_disability_syndrome|not_provided|FG_syndrome_1": 1,
    "FG_syndrome|not_specified|not_provided": 1,
    "not_provided|Nonspecific_Intellectual_Disability|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome|not_provided|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Intellectual_disability": 1,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "not_provided|MED12-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FG_syndrome": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|MED12-related_disorder|FG_syndrome": 1,
    "FG_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome|not_provided": 1,
    "not_specified|FG_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|History_of_neurodevelopmental_disorder": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome_1|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome_1|MED12-related_disorder": 1,
    "not_specified|FG_syndrome_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "not_provided|MED12-related_disorder|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome|Congenital_anomaly_of_kidney_and_urinary_tract": 1,
    "not_specified|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "MED12-related_disorder|not_provided|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome": 1,
    "not_specified|FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|FG_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|MED12-related_disorder": 1,
    "FG_syndrome|MED12-related_intellectual_disability_syndrome|Neurodevelopmental_disorder|X-linked_intellectual_disability_with_marfanoid_habitus|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "FG_syndrome|not_provided|MED12-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|FG_syndrome|not_provided": 1,
    "FG_syndrome|MED12-related_intellectual_disability_syndrome|X-linked_intellectual_disability_with_marfanoid_habitus": 1,
    "FG_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|MED12-related_intellectual_disability_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|FG_syndrome": 1,
    "not_specified|FG_syndrome|Cholestasis-pigmentary_retinopathy-cleft_palate_syndrome|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type|X-linked_intellectual_disability_with_marfanoid_habitus|FG_syndrome_1": 1,
    "X-linked_intellectual_disability_with_marfanoid_habitus|MED12-related_disorder|FG_syndrome": 1,
    "FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "not_provided|FG_syndrome_1|Blepharophimosis_-_intellectual_disability_syndrome|_MKB_type": 1,
    "Inborn_genetic_diseases|not_provided|Cone-rod_dystrophy|Intellectual_disability|not_specified": 1,
    "Autism|_susceptibility_to|_X-linked_1": 13,
    "NLGN3-related_disorder": 2,
    "Inborn_genetic_diseases|NLGN3-related_disorder|not_provided": 1,
    "NLGN3-related_disorder|Inborn_genetic_diseases": 2,
    "NLGN3-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|NLGN3-related_disorder|not_specified": 1,
    "not_provided|NLGN3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|NLGN3-related_disorder": 1,
    "NLGN3-related_disorder|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Autism_spectrum_disorder|NLGN3-related_disorder": 1,
    "NLGN3-related_disorder|not_provided": 1,
    "NLGN3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|not_provided": 23,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 10,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1": 46,
    "GJB1-related_disorder|Charcot-Marie-Tooth_Neuropathy_X": 2,
    "GJB1-related_disorder": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 6,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 4,
    "GJB1-related_disorder|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided": 1,
    "Charcot-Marie-Tooth_Neuropathy_X": 421,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease": 55,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided": 3,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 18,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_Neuropathy_X": 3,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_Neuropathy_X": 2,
    "Charcot-Marie-Tooth_disease-hearing_loss-intellectual_disability_syndrome|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease": 4,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 27,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided": 3,
    "not_specified|Charcot-Marie-Tooth_Neuropathy_X": 5,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 32,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X": 2,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 9,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 8,
    "GJB1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 2,
    "Charcot-Marie-Tooth_Neuropathy_X|Distal_sensory_impairment|Talipes_cavus_equinovarus|Reduced_tendon_reflexes|Progressive_distal_muscular_atrophy|Progressive_distal_muscle_weakness|Hammertoe|Achilles_tendon_contracture|Pain|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 2,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 2,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X": 8,
    "not_provided|not_specified|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X": 22,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X": 5,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 5,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 2,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|Peripheral_neuropathy": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "GJB1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Dejerine-Sottas_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_Neuropathy_X": 2,
    "GJB1-related_disorder|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases": 3,
    "Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 6,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 4,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 2,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Inborn_genetic_diseases|not_provided": 1,
    "Hand_muscle_atrophy": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided|GJB1-related_disorder|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|not_specified": 3,
    "Peripheral_neuropathy|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Cerebellar_ataxia": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Dejerine-Sottas_disease": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 2,
    "Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Inborn_genetic_diseases|not_provided": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Peripheral_neuropathy": 1,
    "Decreased_nerve_conduction_velocity|Sensory_neuropathy|Distal_muscle_weakness|Pes_cavus|Hammertoe|Charcot-Marie-Tooth_Neuropathy_X|Peroneal_muscle_atrophy|Distal_lower_limb_muscle_weakness|Hand_muscle_atrophy|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|GJB1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided|Charcot-Marie-Tooth_disease": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|not_provided|Charcot-Marie-Tooth_disease_X-linked_dominant_1": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|not_specified|Charcot-Marie-Tooth_disease|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "GJB1-related_disorder|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|not_provided|not_specified": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_X-linked_dominant_1|GJB1-related_disorder|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|not_specified": 1,
    "Charcot-Marie-Tooth_disease|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Charcot-Marie-Tooth_disease_X-linked_dominant_1|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|not_specified|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease|Charcot-Marie-Tooth_disease_X-linked_dominant_1|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 1,
    "ZMYM3-related_disorder": 14,
    "Intellectual_developmental_disorder|_X-linked_112": 8,
    "Intellectual_developmental_disorder|_X-linked_112|not_specified": 1,
    "ZMYM3-related_disorder|not_provided": 2,
    "not_provided|ZMYM3-related_disorder": 3,
    "not_provided|Global_developmental_delay|Abnormal_facial_shape|Hyporeflexia|Neonatal_hypotonia": 1,
    "Intellectual_developmental_disorder|_X-linked_112|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_34|not_provided|Intellectual_disability": 1,
    "Syndromic_X-linked_intellectual_disability_34": 22,
    "not_specified|See_cases|not_provided": 1,
    "NONO-related_disorder": 2,
    "not_provided|Syndromic_X-linked_intellectual_disability_34": 2,
    "Non-ossifying_fibromas_with_pathologic_factures_and_X-linked_intellectual_disability": 1,
    "Syndromic_X-linked_intellectual_disability_34|Inborn_genetic_diseases|not_provided": 1,
    "NONO-related_disorder|not_provided": 2,
    "Medulloblastoma|Syndromic_X-linked_intellectual_disability_34": 1,
    "not_provided|NONO-related_disorder": 2,
    "not_provided|Syndromic_X-linked_intellectual_disability_34|Inborn_genetic_diseases": 1,
    "NONO-related_disorder|Inborn_genetic_diseases": 1,
    "TAF1-related_disorder|not_specified|not_provided": 1,
    "Heart|_malformation_of|Intellectual_disability|_X-linked|_syndromic_33": 2,
    "not_provided|TAF1-related_disorder": 10,
    "not_provided|Intellectual_disability|_X-linked|_syndromic_33": 8,
    "X-linked_dystonia-parkinsonism|not_provided|TAF1-related_disorder": 1,
    "Intellectual_disability|_X-linked|_syndromic_33": 43,
    "TAF1-related_disorder": 10,
    "TAF1-related_syndromic_intellectual_disability": 1,
    "TAF1-related_X-linked_syndromic_intellectual_disability": 1,
    "not_provided|X-linked_dystonia-parkinsonism|Intellectual_disability|_X-linked|_syndromic_33": 3,
    "Intellectual_disability|_X-linked|_syndromic_33|not_provided": 11,
    "Intellectual_disability|_X-linked|_syndromic_33|Inborn_genetic_diseases": 2,
    "X-linked_dystonia-parkinsonism": 4,
    "TAF1-related_disorder|not_provided": 10,
    "not_provided|TAF1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|TAF1-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "Intellectual_disability|_X-linked|_syndromic_33|Heart|_malformation_of": 6,
    "X-linked_dystonia-parkinsonism|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "not_provided|Intellectual_disability|_X-linked|_syndromic_33|Inborn_genetic_diseases": 1,
    "Speech_and_developmental_delays": 1,
    "not_provided|X-linked_dystonia-parkinsonism": 1,
    "Autism_spectrum_disorder|not_provided|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "Intellectual_disability|_X-linked|_syndromic_33|X-linked_dystonia-parkinsonism": 1,
    "TAF1-related_syndromic_intellectual_disability|Intellectual_disability|_X-linked|_syndromic_33|Heart|_malformation_of": 1,
    "Intellectual_disability|_X-linked|_syndromic_33|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Heart|_malformation_of|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "not_provided|Inborn_genetic_diseases|TAF1-related_disorder": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|not_provided|TAF1-related_disorder": 1,
    "not_provided|not_specified|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "Intellectual_disability|_X-linked|_syndromic_33|not_provided|Heart|_malformation_of": 1,
    "X-linked_dystonia-parkinsonism|Heart|_malformation_of": 1,
    "not_provided|Intellectual_disability|_X-linked|_syndromic_33|Heart|_malformation_of": 1,
    "Heart|_malformation_of|Intellectual_disability|_X-linked|_syndromic_33|not_provided": 1,
    "X-linked_dystonia-parkinsonism|not_provided": 1,
    "Marfanoid_habitus_and_intellectual_disability|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "TAF1-related_disorder|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "TAF1-related_disorder|Intellectual_disability|_X-linked|_syndromic_33|X-linked_dystonia-parkinsonism|not_provided": 1,
    "not_provided|TAF1-related_disorder|X-linked_dystonia-parkinsonism|Intellectual_disability|_X-linked|_syndromic_33": 1,
    "not_provided|Intellectual_disability|_X-linked|_syndromic_33|X-linked_dystonia-parkinsonism|Intellectual_disability": 1,
    "TAF1-related_disorder|X-linked_dystonia-parkinsonism": 1,
    "Intellectual_disability|_X-linked_106": 30,
    "Intellectual_disability|_X-linked_106|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_106|not_provided": 1,
    "OGT-related_disorder": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_106": 2,
    "not_provided|Intellectual_disability|_X-linked_106": 5,
    "OGT-related_disorder|not_provided": 2,
    "OGT-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Intellectual_disability|_X-linked_106": 1,
    "OGT-related_X-linked_syndromic_intellectual_disability": 1,
    "not_provided|OGT-related_disorder": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_106|not_provided": 1,
    "Non-obstructive_azoospermia|Spermatogenic_failure|_X-linked|_4": 2,
    "Spermatogenic_failure|_X-linked|_4": 1,
    "Spermatogenic_failure|_X-linked|_4|Azoospermia": 1,
    "Spinocerebellar_ataxia|_X-linked": 2,
    "Cornelia_de_Lange_syndrome_5|Inborn_genetic_diseases": 9,
    "Cornelia_de_Lange_syndrome_5": 205,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_5": 8,
    "Cornelia_de_Lange_syndrome_5|not_provided": 6,
    "Inborn_genetic_diseases|not_specified|not_provided|Cornelia_de_Lange_syndrome_5|Intellectual_disability": 1,
    "Cornelia_de_Lange_syndrome_5|Cornelia_de_Lange_syndrome_1": 1,
    "HDAC8-related_disorder|Cornelia_de_Lange_syndrome_5": 2,
    "Inborn_genetic_diseases|not_provided|Cornelia_de_Lange_syndrome_5": 4,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_5|not_provided": 1,
    "not_provided|Cornelia_de_Lange_syndrome_5": 11,
    "Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_5|HDAC8-related_disorder": 2,
    "Atrial_septal_defect|4-5_finger_cutaneous_syndactyly|Polycystic_kidney_disease|Abnormality_of_the_face|Intellectual_disability|Clinodactyly_of_the_5th_finger": 1,
    "Cornelia_de_Lange_syndrome_1|not_provided|Global_developmental_delay|Fetal_growth_restriction|Delayed_speech_and_language_development|Sparse_scalp_hair|Abnormal_facial_shape|Microcephaly|Inborn_genetic_diseases": 1,
    "not_provided|Cornelia_de_Lange_syndrome_5|not_specified": 1,
    "HDAC8-related_disorder": 1,
    "Cornelia_de_Lange_syndrome_5|HDAC8-related_disorder": 2,
    "Cornelia_de_Lange_syndrome_5|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Cornelia_de_Lange_syndrome_5": 1,
    "Cornelia_de_Lange_syndrome_5|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Cornelia_de_Lange_syndrome_5|not_provided": 1,
    "Glycogen_storage_disease_IXd": 364,
    "not_provided|Glycogen_storage_disease_IXd": 16,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXd": 18,
    "Glycogen_storage_disease_IXd|Inborn_genetic_diseases": 17,
    "not_specified|not_provided|PHKA1-related_disorder|Glycogen_storage_disease_IXd": 1,
    "Glycogen_storage_disease_IXd|not_provided": 27,
    "Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_IXd": 3,
    "Glycogen_storage_disease_IXd|PHKA1-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Glycogen_storage_disease_IXd": 5,
    "Glycogen_storage_disease_IXd|not_specified": 8,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXd|not_provided": 2,
    "not_specified|Glycogen_storage_disease_IXd": 5,
    "PHKA1-related_disorder|Inborn_genetic_diseases|Glycogen_storage_disease_IXd": 1,
    "not_provided|Glycogen_storage_disease_IXd|Inborn_genetic_diseases": 1,
    "PHKA1-related_disorder|Glycogen_storage_disease_IXd": 4,
    "not_specified|not_provided|Glycogen_storage_disease_IXd": 1,
    "PHKA1-related_disorder": 4,
    "not_specified|Glycogen_storage_disease_IXd|PHKA1-related_disorder|not_provided": 1,
    "not_provided|not_specified|Glycogen_storage_disease_IXd": 1,
    "Glycogen_storage_disease_IXd|Glycogen_phosphorylase_kinase_deficiency|not_provided": 1,
    "Glycogen_phosphorylase_kinase_deficiency|Glycogen_storage_disease_IXd": 1,
    "not_provided|Glycogen_storage_disease_IXd|not_specified": 2,
    "not_specified|Glycogen_storage_disease_IXd|PHKA1-related_disorder": 1,
    "Glycogen_storage_disease_IXd|Spinocerebellar_ataxia|_X-linked": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_IXd|not_specified": 2,
    "Glycogen_storage_disease_IXd|not_provided|PHKA1-related_disorder": 2,
    "Glycogen_storage_disease_IXd|PHKA1-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Glycogen_storage_disease_IXd|not_provided": 1,
    "Inborn_genetic_diseases|Peripheral_neuropathy": 1,
    "not_specified|PHKA1-related_disorder": 1,
    "not_provided|Glycogen_storage_disease_IXd|PHKA1-related_disorder": 1,
    "Glycogen_storage_disease_IXd|Glycogen_phosphorylase_kinase_deficiency": 1,
    "Glycogen_storage_disease_IXd|not_provided|Inborn_genetic_diseases": 2,
    "Glycogen_storage_disease_IXd|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Glycogen_storage_disease_IXd": 1,
    "CDX4-related_disorder": 1,
    "XIST-related_disorder": 32,
    "TSIX-related_disorder": 8,
    "XIST-related_disorder|not_provided": 1,
    "not_provided|X_inactivation|_familial_skewed|_1": 1,
    "ZCCHC13-related_disorder": 2,
    "ZCCHC13-related_disorder|not_provided": 1,
    "Spastic_paraplegia|not_provided|Allan-Herndon-Dudley_syndrome|Inborn_genetic_diseases": 1,
    "Allan-Herndon-Dudley_syndrome": 62,
    "SLC16A2-related_disorder": 4,
    "Spastic_paraplegia|Allan-Herndon-Dudley_syndrome": 3,
    "Allan-Herndon-Dudley_syndrome|Spastic_paraplegia": 2,
    "Spastic_paraplegia|Allan-Herndon-Dudley_syndrome|Inborn_genetic_diseases|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Allan-Herndon-Dudley_syndrome|not_specified": 1,
    "not_provided|Spastic_paraplegia|Allan-Herndon-Dudley_syndrome": 1,
    "not_provided|SLC16A2-related_disorder|Spastic_paraplegia|not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|Inborn_genetic_diseases|Allan-Herndon-Dudley_syndrome|not_specified|not_provided": 1,
    "not_provided|Allan-Herndon-Dudley_syndrome|Spastic_paraplegia": 2,
    "not_specified|Allan-Herndon-Dudley_syndrome": 1,
    "Spastic_paraplegia|Allan-Herndon-Dudley_syndrome|not_provided": 1,
    "SLC16A2-related_disorder|Spastic_paraplegia|Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia|Intellectual_disability": 1,
    "not_provided|Allan-Herndon-Dudley_syndrome": 4,
    "Spastic_paraplegia|Inborn_genetic_diseases|not_provided|Allan-Herndon-Dudley_syndrome": 1,
    "Allan-Herndon-Dudley_syndrome|not_provided": 3,
    "Spastic_paraplegia|not_specified|Allan-Herndon-Dudley_syndrome|not_provided|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|not_provided|Allan-Herndon-Dudley_syndrome": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified|not_provided|Intellectual_disability": 1,
    "Spastic_paraplegia|not_provided|Allan-Herndon-Dudley_syndrome|Decreased_activity_of_the_pyruvate_dehydrogenase_complex": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_spastic_paraplegia|Allan-Herndon-Dudley_syndrome|not_provided": 1,
    "History_of_neurodevelopmental_disorder|Spastic_paraplegia": 1,
    "Allan-Herndon-Dudley_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Allan-Herndon-Dudley_syndrome|not_provided|Spastic_paraplegia": 1,
    "Allan-Herndon-Dudley_syndrome|not_provided|Spastic_paraplegia": 1,
    "not_specified|Allan-Herndon-Dudley_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Allan-Herndon-Dudley_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Spastic_paraplegia|Hereditary_spastic_paraplegia": 1,
    "not_provided|Intellectual_disability|_X-linked_61": 3,
    "Intellectual_disability|_X-linked_61": 16,
    "Intellectual_disability|_X-linked_61|not_provided": 4,
    "not_provided|Non-syndromic_X-linked_intellectual_disability|Inborn_genetic_diseases|Intellectual_disability|_X-linked_61": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_61": 1,
    "Global_developmental_delay|Intellectual_disability|_X-linked_61|Non-syndromic_X-linked_intellectual_disability": 1,
    "Intellectual_disability|_X-linked_61|Inborn_genetic_diseases": 2,
    "RLIM-related_disorder": 2,
    "not_provided|RLIM-related_syndromic_intellectual_disability": 1,
    "not_provided|NEXMIF-related_disorder": 2,
    "NEXMIF-related_disorder|not_specified|not_provided": 4,
    "NEXMIF-related_disorder|not_provided": 5,
    "NEXMIF-related_disorder": 6,
    "not_provided|X-linked_intellectual_disability|_Cantagrel_type": 16,
    "X-linked_intellectual_disability|_Cantagrel_type": 72,
    "not_specified|not_provided|NEXMIF-related_disorder": 1,
    "not_provided|X-linked_intellectual_disability|_Cantagrel_type|not_specified": 3,
    "not_specified|NEXMIF-related_disorder|not_provided": 2,
    "NEXMIF-related_disorder|not_provided|not_specified": 3,
    "not_provided|not_specified|NEXMIF-related_disorder": 1,
    "X-linked_intellectual_disability|_Cantagrel_type|not_provided": 13,
    "NEXMIF-related_disorder|X-linked_intellectual_disability|_Cantagrel_type|not_specified|not_provided": 1,
    "not_specified|NEXMIF-related_disorder|X-linked_intellectual_disability|_Cantagrel_type|not_provided": 1,
    "not_specified|not_provided|X-linked_intellectual_disability|_Cantagrel_type": 2,
    "not_provided|not_specified|X-linked_intellectual_disability|_Cantagrel_type": 1,
    "X-linked_intellectual_disability|_Cantagrel_type|not_provided|not_specified": 2,
    "X-linked_intellectual_disability|_Cantagrel_type|not_specified|not_provided": 11,
    "not_provided|Inborn_genetic_diseases|X-linked_intellectual_disability|_Cantagrel_type": 1,
    "not_provided|X-linked_intellectual_disability|_Cantagrel_type|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|X-linked_intellectual_disability|_Cantagrel_type|not_provided": 1,
    "not_provided|NEXMIF-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|X-linked_intellectual_disability|_Cantagrel_type|not_provided|Seizure": 1,
    "X-linked_intellectual_disability|_Cantagrel_type|not_specified": 1,
    "not_specified|X-linked_intellectual_disability|_Cantagrel_type|not_provided": 1,
    "Intellectual_disability|X-linked_intellectual_disability|_Cantagrel_type": 1,
    "not_specified|not_provided|X-linked_intellectual_disability|_Cantagrel_type|Continuous_spike_and_waves_during_slow_sleep": 1,
    "X-linked_sideroblastic_anemia_with_ataxia": 15,
    "ABCB7-related_disorder": 2,
    "Inborn_genetic_diseases|Spinocerebellar_ataxia|_X-linked": 1,
    "not_provided|X-linked_sideroblastic_anemia_with_ataxia": 6,
    "not_provided|ABCB7-related_disorder": 2,
    "not_specified|Sideroblastic_Anemia_and_Ataxia|not_provided": 1,
    "Sideroblastic_Anemia_and_Ataxia|not_provided|X-linked_sideroblastic_anemia_with_ataxia|not_specified": 2,
    "not_provided|X-linked_sideroblastic_anemia_with_ataxia|Inborn_genetic_diseases": 1,
    "ABCB7-related_disorder|not_provided|not_specified|Intellectual_disability": 1,
    "ABCB7-related_disorder|not_provided|Sideroblastic_Anemia_and_Ataxia|X-linked_sideroblastic_anemia_with_ataxia|not_specified": 1,
    "ABCB7-related_disorder|not_specified|not_provided|X-linked_sideroblastic_anemia_with_ataxia": 1,
    "Inborn_genetic_diseases|ABCB7-related_disorder": 1,
    "Sideroblastic_Anemia_and_Ataxia|X-linked_sideroblastic_anemia_with_ataxia|not_specified|not_provided": 1,
    "ABCB7-related_disorder|Sideroblastic_Anemia_and_Ataxia|not_specified|not_provided": 1,
    "X-linked_sideroblastic_anemia_with_ataxia|not_provided": 2,
    "not_specified|ABCB7-related_disorder|not_provided|Sideroblastic_Anemia_and_Ataxia": 1,
    "ABCB7-related_disorder|not_provided": 1,
    "ABCB7-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked_91": 1,
    "Spastic_diplegia": 1,
    "ZDHHC15-related_condition": 1,
    "Syndactyly_type_8|not_provided": 1,
    "FGF16-related_disorder": 1,
    "Syndactyly_type_8": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1651,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 87,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder": 9,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases": 11,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Inborn_genetic_diseases": 1,
    "not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 20,
    "ATRX-related_disorder": 19,
    "Inborn_genetic_diseases|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder": 2,
    "Global_developmental_delay|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked": 4,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 3,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified": 18,
    "not_provided|ATRX-related_disorder|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 5,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 10,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 11,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "ATRX-related_disorder|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 10,
    "Inborn_genetic_diseases|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases": 38,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified": 2,
    "Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 27,
    "Acquired_hemoglobin_H_disease|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 3,
    "not_provided|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 3,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|not_provided": 3,
    "ATRX-related_disorder|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 3,
    "not_specified|not_provided|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|not_provided|ATRX-related_disorder|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Abnormality_of_the_nervous_system|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|not_provided": 4,
    "Inborn_genetic_diseases|History_of_neurodevelopmental_disorder|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|ATRX-related_disorder": 1,
    "ATR-X-related_syndrome": 4,
    "not_specified|not_provided|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "not_provided|See_cases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 2,
    "Astrocytoma|_anaplastic|Atypical_teratoid_rhabdoid_tumor|not_provided|Inborn_genetic_diseases|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 1,
    "Acquired_hemoglobin_H_disease|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Neonatal_hypotonia": 1,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder|Inborn_genetic_diseases": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 2,
    "Inborn_genetic_diseases|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "not_provided|ATRX-related_disorder|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 3,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder": 2,
    "Drooling|Psychomotor_deterioration|Generalized_hypotonia|Low-set|_posteriorly_rotated_ears|Absent_speech|Microcephaly|Short_stature": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 7,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Inborn_genetic_diseases": 4,
    "not_provided|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|ATRX-related_disorder|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 8,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Inborn_genetic_diseases": 2,
    "ATRX-related_disorder|Alpha-thalassemia/intellectual_disability_syndrome|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|not_provided": 5,
    "not_provided|Inborn_genetic_diseases|ATRX-related_disorder|Intellectual_disability|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "not_provided|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 3,
    "Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 7,
    "not_provided|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 5,
    "ATRX-related_disorder|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease|not_provided": 1,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_specified": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|ATRX-related_disorder|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 1,
    "ATRX-related_disorder|not_specified|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|ATRX-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|ATRX-related_disorder|not_specified|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|ATRX-related_disorder|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|not_specified": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|not_provided|ATRX-related_disorder|Inborn_genetic_diseases": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Developmental_disorder|ATRX-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|ATRX-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease": 1,
    "Acquired_hemoglobin_H_disease|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|ATRX-related_disorder|Inborn_genetic_diseases": 1,
    "Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability": 1,
    "ATRX-related_disorder|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|not_provided|Alpha_thalassemia_X-linked_intellectual_disability_(ATRX)_syndrome|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "not_specified|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 2,
    "not_provided|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases": 2,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified": 2,
    "not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Inborn_genetic_diseases|ATRX-related_disorder": 1,
    "not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Inborn_genetic_diseases": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 2,
    "ATRX-related_disorder|Inborn_genetic_diseases|not_specified|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease|not_provided|Intellectual_disability": 1,
    "Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATR-X-related_syndrome": 3,
    "not_specified|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases": 1,
    "Intellectual_disability|ATRX-related_disorder|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "not_specified|Inborn_genetic_diseases|ATRX-related_disorder|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Microcephaly|Global_developmental_delay": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|ATRX-related_disorder": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "ATRX-related_disorder|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified": 1,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder|ATR-X-related_syndrome": 1,
    "ATRX-related_disorder|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|ATRX-related_disorder|not_provided": 1,
    "not_specified|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1": 1,
    "not_specified|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|ATR-X-related_syndrome|ATRX-related_disorder|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided": 1,
    "not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Inborn_genetic_diseases|not_specified|ATRX-related_disorder": 1,
    "ATRX-related_disorder|not_specified": 1,
    "Renier-Gabreels-Jasper_syndrome|Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|Alpha_thalassemia-X-linked_intellectual_disability_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease|not_specified": 1,
    "Global_developmental_delay|Microcephaly": 1,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|Acquired_hemoglobin_H_disease": 1,
    "Acquired_hemoglobin_H_disease": 3,
    "Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|Inborn_genetic_diseases|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Acquired_hemoglobin_H_disease|not_provided": 1,
    "Inborn_genetic_diseases|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_specified|ATRX-related_disorder": 1,
    "Alpha-thalassemia/intellectual_disability_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Acquired_hemoglobin_H_disease|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|_1|Alpha_thalassemia-X-linked_intellectual_disability_syndrome|not_provided|Intellectual_disability-hypotonic_facies_syndrome|_X-linked|Intellectual_disability": 1,
    "not_provided|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 8,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|not_provided|Inherited_Immunodeficiency_Diseases": 1,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 186,
    "Congenital_disorder_of_glycosylation|_type_ICC|Congenital_disorder_of_glycosylation": 1,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|Congenital_disorder_of_glycosylation|_type_ICC|MAGT1-related_disorder|not_specified": 1,
    "Congenital_disorder_of_glycosylation|_type_ICC|Congenital_disorder_of_glycosylation|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 1,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|Inborn_genetic_diseases": 6,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|Congenital_disorder_of_glycosylation|_type_ICC": 2,
    "MAGT1-related_disorder|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 4,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|not_provided": 5,
    "Congenital_disorder_of_glycosylation|_type_ICC": 1,
    "MAGT1-related_disorder": 2,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|not_provided": 1,
    "MAGT1-related_disorder|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|Inborn_genetic_diseases": 1,
    "Congenital_disorder_of_glycosylation|_type_ICC|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 1,
    "Inborn_genetic_diseases|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 2,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|Linear_skin_defects_with_multiple_congenital_anomalies_2|Congenital_disorder_of_glycosylation|_type_ICC": 1,
    "not_provided|not_specified|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 1,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|Inborn_genetic_diseases|Congenital_disorder_of_glycosylation|_type_ICC": 2,
    "not_specified|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 1,
    "Inborn_genetic_diseases|not_specified|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|not_provided": 1,
    "not_provided|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|MAGT1-related_disorder": 1,
    "not_specified|Inborn_genetic_diseases|X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia": 1,
    "X-linked_immunodeficiency_with_magnesium_defect|_Epstein-Barr_virus_infection_and_neoplasia|MAGT1-related_disorder": 1,
    "Linear_skin_defects_with_multiple_congenital_anomalies_2": 4,
    "not_provided|Linear_skin_defects_with_multiple_congenital_anomalies_2": 1,
    "COX7B-related_disorder|not_specified|not_provided": 1,
    "COX7B-related_disorder": 1,
    "not_provided|ATP7A-related_disorder": 2,
    "not_provided|Menkes_kinky-hair_syndrome": 5,
    "ATP7A-related_disorder": 3,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 173,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 234,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 347,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Inborn_genetic_diseases|not_provided": 1,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 160,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|Inborn_genetic_diseases": 3,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome": 61,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 269,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 6,
    "Menkes_kinky-hair_syndrome": 296,
    "not_provided|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 8,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 19,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_provided": 14,
    "Ehlers-Danlos_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|ATP7A-related_disorder|not_provided": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 29,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome": 1,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Inborn_genetic_diseases|Ehlers-Danlos_syndrome": 1,
    "Menkes_kinky-hair_syndrome|not_provided|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 1,
    "not_specified|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 1,
    "Menkes_kinky-hair_syndrome|not_provided|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|ATP7A-related_disorder": 1,
    "Ehlers-Danlos_syndrome|not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder": 1,
    "ATP7A-related_disorder|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_provided|not_specified": 1,
    "not_provided|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Neuronopathy|_distal_hereditary_motor|_autosomal_dominant_1": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 4,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases": 3,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 7,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 4,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|ATP7A-related_disorder": 3,
    "X-linked_distal_spinal_muscular_atrophy_type_3": 10,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_provided|Inborn_genetic_diseases": 2,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Inborn_genetic_diseases": 6,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_specified|not_provided|Inborn_genetic_diseases": 2,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_specified": 2,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases": 3,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_provided": 12,
    "Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 4,
    "not_provided|Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 1,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_provided|not_specified|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome": 1,
    "not_specified|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|not_provided|ATP7A-related_disorder": 1,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|not_specified": 6,
    "Inborn_genetic_diseases|ATP7A-realted_disorder|Menkes_kinky-hair_syndrome|ATP7A-related_disorder|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 1,
    "not_specified|Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder": 2,
    "Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_provided": 3,
    "not_provided|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 9,
    "Inborn_genetic_diseases|not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 4,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Ehlers-Danlos_syndrome|not_provided": 1,
    "ATP7A-related_disorder|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided|See_cases|Inborn_genetic_diseases": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome": 1,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|not_provided": 5,
    "not_specified|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|not_provided|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "ATP7A-related_disorder|Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_specified|not_provided": 1,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder|not_provided": 1,
    "not_provided|not_specified|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "not_provided|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 4,
    "Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|ATP7A-related_disorder|not_provided": 1,
    "not_specified|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|ATP7A-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Au-Kline_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "not_specified|not_provided|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "not_provided|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 8,
    "not_specified|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 4,
    "not_specified|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 3,
    "not_provided|Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 2,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|not_provided": 2,
    "ATP7A-related_disorder|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 2,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Ehlers-Danlos_syndrome": 2,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|ATP7A-related_disorder|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|not_provided": 4,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Ehlers-Danlos_syndrome": 1,
    "not_provided|Ehlers-Danlos_syndrome|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Ehlers-Danlos_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "Cutis_laxa|_X-linked": 17,
    "Ehlers-Danlos_syndrome|not_provided|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "Menkes_kinky-hair_syndrome|not_provided|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 4,
    "Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 1,
    "Menkes_kinky-hair_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder": 1,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_specified|Inborn_genetic_diseases": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Inborn_genetic_diseases": 7,
    "Cutis_laxa|_X-linked|not_specified": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 3,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_specified": 1,
    "Inborn_genetic_diseases|Ehlers-Danlos_syndrome|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Ehlers-Danlos_syndrome|not_specified": 1,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|ATP7A-related_disorder|Inborn_genetic_diseases": 2,
    "not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Inborn_genetic_diseases": 3,
    "not_provided|Menkes_kinky-hair_syndrome|ATP7A-related_disorder|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 1,
    "Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 4,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "Menkes_kinky-hair_syndrome|ATP7A-related_disorder|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Intellectual_disability|not_provided": 1,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome": 2,
    "Menkes_kinky-hair_syndrome|Menkes_disease|_copper-replacement_responsive": 1,
    "Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 2,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 2,
    "ATP7A-related_disorder|Inborn_genetic_diseases|not_provided|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_specified": 2,
    "not_specified|not_provided|History_of_neurodevelopmental_disorder|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "not_specified|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "ATP7A-related_disorder|not_provided|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|not_provided": 2,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome": 1,
    "Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_specified|not_provided": 1,
    "ATP7A-related_disorder|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "ATP7A-related_disorder|Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_specified|not_provided": 1,
    "ATP7A-related_disorder|Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|not_provided": 1,
    "not_provided|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 2,
    "ATP7A-related_disorder|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 2,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked": 1,
    "not_provided|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|ATP7A-related_disorder|Inborn_genetic_diseases": 1,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_provided|Inborn_genetic_diseases": 1,
    "ATP7A-related_disorder|Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "ATP7A-related_disorder|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 1,
    "not_specified|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided|ATP7A-related_disorder": 1,
    "not_provided|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome": 1,
    "not_specified|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "not_specified|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided": 1,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|ATP7A-related_disorder": 1,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_specified": 1,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided|Inborn_genetic_diseases": 1,
    "ATP7A-related_disorder|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_specified|not_provided": 1,
    "Intellectual_disability|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "Ehlers-Danlos_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_provided": 1,
    "not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Ehlers-Danlos_syndrome|Inborn_genetic_diseases": 1,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Ehlers-Danlos_syndrome": 1,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_provided|ATP7A-related_disorder": 1,
    "ATP7A-related_disorder|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|not_provided|See_cases": 1,
    "not_specified|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|ATP7A-related_disorder": 1,
    "Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder|not_specified": 1,
    "Ehlers-Danlos_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|not_provided": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|Menkes_kinky-hair_syndrome": 1,
    "not_provided|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "Inborn_genetic_diseases|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Ehlers-Danlos_syndrome|not_specified|not_provided": 1,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Ehlers-Danlos_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Intellectual_disability|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome": 1,
    "Menkes_disease|_mild|Menkes_kinky-hair_syndrome": 1,
    "Charcot-Marie-Tooth_disease|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|Ehlers-Danlos_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked": 1,
    "Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3|ATP7A-related_disorder|Inborn_genetic_diseases": 1,
    "Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Cutis_laxa|_X-linked|History_of_neurodevelopmental_disorder|not_provided": 1,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Menkes_kinky-hair_syndrome|Inborn_genetic_diseases|Cutis_laxa|_X-linked|X-linked_distal_spinal_muscular_atrophy_type_3": 1,
    "ATP7A-related_disorder|Inborn_genetic_diseases|Cutis_laxa|_X-linked|Menkes_kinky-hair_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|not_specified|Ehlers-Danlos_syndrome": 1,
    "X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|not_specified": 1,
    "Ehlers-Danlos_syndrome|X-linked_distal_spinal_muscular_atrophy_type_3|Menkes_kinky-hair_syndrome|Cutis_laxa|_X-linked|Inborn_genetic_diseases": 1,
    "Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|not_provided": 24,
    "not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 14,
    "Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 50,
    "PGK1-related_disorder|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 2,
    "Male_infertility_due_to_obstructive_azoospermia": 1,
    "not_specified|not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 1,
    "Hereditary_skeletal_muscle_disorder|not_provided": 1,
    "not_provided|PGK1-related_disorder|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 1,
    "Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|not_provided|Inborn_genetic_diseases": 3,
    "PGK1-related_disorder|Inborn_genetic_diseases|not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 2,
    "not_provided|PGK1-related_disorder": 3,
    "Inborn_genetic_diseases|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 1,
    "not_specified|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|not_provided": 2,
    "Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|not_provided|PGK1-related_disorder": 2,
    "Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|not_provided": 2,
    "PGK1-related_disorder|Epilepsy|not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 1,
    "PGK1-related_disorder": 3,
    "PGK1-related_disorder|not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 1,
    "Profound_global_developmental_delay|Epileptic_encephalopathy": 1,
    "not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|Inborn_genetic_diseases": 1,
    "Phosphoglycerate_kinase_electrophoretic_variant_PGK_II": 1,
    "not_provided|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency|PGK1-related_disorder": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Glycogen_storage_disease_due_to_phosphoglycerate_kinase_1_deficiency": 1,
    "PGK1-related_disorder|not_provided": 1,
    "GPR174-related_disorder": 5,
    "GPR174-related_disorder|not_provided": 1,
    "not_provided|GPR174-related_disorder": 1,
    "Cleft_palate_with_or_without_ankyloglossia|_X-linked": 21,
    "not_provided|Cleft_palate_with_or_without_ankyloglossia|_X-linked": 4,
    "not_provided|Cleft_palate_with_or_without_ankyloglossia|_X-linked|TBX22-related_disorder": 4,
    "not_provided|TBX22-related_disorder|Cleft_palate_with_or_without_ankyloglossia|_X-linked": 1,
    "TBX22-related_disorder": 6,
    "Cleft_palate_with_ankyloglossia": 9,
    "Inborn_genetic_diseases|Cleft_palate_with_or_without_ankyloglossia|_X-linked": 1,
    "not_provided|TBX22-related_disorder": 1,
    "Cleft_palate|Orofacial_cleft": 1,
    "Abruzzo-Erickson_syndrome|Cleft_palate_with_or_without_ankyloglossia|_X-linked|not_specified": 1,
    "Abruzzo-Erickson_syndrome|not_specified|not_provided|Cleft_palate_with_or_without_ankyloglossia|_X-linked": 1,
    "TBX22-related_disorder|not_specified|not_provided": 1,
    "not_provided|Cleft_palate_with_or_without_ankyloglossia|_X-linked|Abruzzo-Erickson_syndrome": 1,
    "Cleft_palate_with_or_without_ankyloglossia|_X-linked|not_provided": 1,
    "Cleft_palate_with_or_without_ankyloglossia|_X-linked|Inborn_genetic_diseases": 1,
    "Cleft_palate_with_or_without_ankyloglossia|_X-linked|TBX22-related_disorder|not_provided": 1,
    "Cleft_palate_with_or_without_ankyloglossia|_X-linked|TBX22-related_disorder": 1,
    "Intellectual_disability|_X-linked_93": 119,
    "Intellectual_disability|_X-linked_93|not_provided": 12,
    "not_provided|Intellectual_disability|_X-linked_93": 18,
    "Inborn_genetic_diseases|BRWD3-related_disorder|not_provided|Intellectual_disability|_X-linked_93": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Conotruncal_heart_malformations|Intellectual_disability|_X-linked_93|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_X-linked_93|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_93": 2,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_93|BRWD3-related_disorder|not_provided": 1,
    "not_provided|BRWD3-related_disorder": 2,
    "BRWD3-related_disorder|not_provided": 3,
    "not_specified|not_provided|Intellectual_disability|_X-linked_93": 1,
    "BRWD3-related_disorder": 12,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_93": 5,
    "Intellectual_disability|_X-linked_93|not_specified": 1,
    "Intellectual_disability|_X-linked_93|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked_93|not_provided|not_specified": 1,
    "Developmental_delay|Intellectual_disability|_X-linked_93": 1,
    "Intellectual_disability|_X-linked_93|BRWD3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Intellectual_disability|_X-linked_93|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_93|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked_93|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "BRWD3-related_X-linked_syndromic_intellectual_disability": 1,
    "not_provided|Intellectual_disability|_X-linked_93|not_specified": 1,
    "Inborn_genetic_diseases|BRWD3-related_disorder": 1,
    "not_provided|not_specified|Intellectual_disability|_X-linked_93|BRWD3-related_disorder": 1,
    "Intellectual_disability|_X-linked_93|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_93": 1,
    "BRWD3-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|BRWD3-related_disorder": 1,
    "BRWD3-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_X-linked_93|Intellectual_disability": 1,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 94,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided|not_specified|POU3F4-related_disorder": 1,
    "POU3F4-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|POU3F4-related_disorder": 1,
    "Autosomal_recessive_sensorineural_hearing_loss": 1,
    "POU3F4-related_disorder": 1,
    "Inborn_genetic_diseases|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher|Rare_genetic_deafness": 3,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided": 3,
    "POU3F4-related_disorder|not_provided": 1,
    "Nonsyndromic_genetic_hearing_loss|Rare_genetic_deafness|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "not_specified|X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided": 1,
    "not_provided|not_specified|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 1,
    "X-linked_mixed_hearing_loss_with_perilymphatic_gusher|not_provided|not_specified": 1,
    "X-linked_nonsyndromic_hearing_loss": 1,
    "not_provided|X-linked_mixed_hearing_loss_with_perilymphatic_gusher": 2,
    "X-linked_nonsyndromic_hearing_loss|not_provided": 1,
    "Spermatogenic_failure|_X-linked|_8": 1,
    "SATL1-related_disorder": 13,
    "Intellectual_disability|_X-linked_97": 32,
    "not_provided|Intellectual_disability|_X-linked_97": 10,
    "not_provided|Intellectual_disability|_X-linked_97|not_specified": 1,
    "Inborn_genetic_diseases|ZNF711-related_disorder|not_specified": 1,
    "Intellectual_disability|_X-linked_97|Inborn_genetic_diseases": 1,
    "ZNF711-related_disorder|Intellectual_disability|_X-linked_97": 2,
    "ZNF711-related_disorder": 3,
    "Intellectual_disability|_X-linked_97|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_97": 1,
    "See_cases|not_provided|not_specified|Intellectual_disability|_X-linked_97": 1,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_X-linked_97": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_X-linked_97": 1,
    "ZNF711-related_disorder|not_specified|Intellectual_disability|_X-linked_97": 1,
    "ZNF711-related_disorder|not_provided|Inborn_genetic_diseases|Intellectual_disability|_X-linked_97": 1,
    "Intellectual_disability|_X-linked_97|not_provided": 1,
    "Non-syndromic_X-linked_intellectual_disability|Intellectual_disability|_X-linked_97|Premature_ovarian_failure_2B|not_provided": 1,
    "Non-syndromic_X-linked_intellectual_disability|Intellectual_disability|_X-linked_97|Premature_ovarian_failure_2B": 2,
    "Non-syndromic_X-linked_intellectual_disability|not_provided|Premature_ovarian_failure_2B": 2,
    "Non-syndromic_X-linked_intellectual_disability|Premature_ovarian_failure_2B": 2,
    "Premature_ovarian_failure_2B": 23,
    "Non-syndromic_X-linked_intellectual_disability|Premature_ovarian_failure_2B|not_provided": 1,
    "Premature_ovarian_failure_2B|not_provided": 14,
    "not_provided|Premature_ovarian_failure_2B": 2,
    "POF1B-related_disorder": 4,
    "POF1B-related_disorder|Premature_ovarian_failure_2B": 1,
    "Premature_ovarian_failure_2B|POF1B-related_disorder|not_provided": 1,
    "POF1B-related_disorder|Premature_ovarian_failure_2B|not_provided": 2,
    "not_provided|Premature_ovarian_insufficiency|Premature_ovarian_failure_2B": 1,
    "Premature_ovarian_failure_2B|not_specified": 1,
    "POF1B-related_disorder|not_provided": 1,
    "Premature_ovarian_failure_2B|not_specified|not_provided": 1,
    "not_provided|Choroideremia": 35,
    "not_provided|Choroideremia|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Choroideremia|not_provided": 2,
    "not_provided|Choroideremia|Retinal_dystrophy": 1,
    "not_specified|not_provided|Choroideremia": 1,
    "Choroideremia|_Salla_type|Choroideremia": 1,
    "Choroideremia|Retinal_dystrophy|not_provided": 3,
    "Choroideremia|not_provided|CHM-related_disorder": 1,
    "Retinal_dystrophy|not_provided|Choroideremia": 6,
    "Retinal_dystrophy|Choroideremia": 3,
    "CHM-related_disorder|not_provided|Retinal_dystrophy": 1,
    "CHM-related_disorder|not_provided": 2,
    "Retinal_dystrophy|Choroideremia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|not_specified|Choroideremia": 1,
    "CHM-related_disorder|Choroideremia|not_provided": 1,
    "CHM-related_disorder|Retinitis_pigmentosa|Choroideremia|Retinal_dystrophy|not_provided": 1,
    "not_provided|Choroideremia|CHM-related_disorder": 1,
    "Choroideremia|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Choroideremia": 1,
    "Choroideremia|Retinal_dystrophy|not_provided|not_specified": 1,
    "Choroideremia|Abnormality_of_the_eye|Retinal_dystrophy": 1,
    "Choroideremia|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Choroideremia": 1,
    "not_provided|CHM-related_disorder": 1,
    "Retinal_dystrophy|Choroideremia|not_provided": 1,
    "Chorioretinal_atrophy|Night_blindness": 1,
    "not_specified|PCDH11X-related_disorder": 1,
    "not_provided|Premature_ovarian_failure_2A": 1,
    "Premature_ovarian_failure_2A": 5,
    "DIAPH2-related_disorder": 4,
    "DIAPH2-related_disorder|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_9|not_provided": 4,
    "Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases": 18,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9": 84,
    "PCDH19-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_specified|PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_9|not_specified": 17,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases|PCDH19-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_9|not_provided": 69,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9|not_specified": 6,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 7,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Self-limited_epilepsy_with_centrotemporal_spikes|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases": 5,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases": 1,
    "PCDH19-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 3,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_9": 2,
    "Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_9": 15,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9": 22,
    "Developmental_and_epileptic_encephalopathy|_9|PCDH19-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_9|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_9|PCDH19-related_disorder": 2,
    "PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 5,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9": 3,
    "PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9": 2,
    "PCDH19-related_epilepsy|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_9": 6,
    "Complex_febrile_seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Abnormal_cerebral_morphology": 2,
    "Intellectual_disability|Inborn_genetic_diseases|PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Inborn_genetic_diseases|PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9|not_provided": 1,
    "Glycine_encephalopathy|Developmental_and_epileptic_encephalopathy|_9": 6,
    "PCDH19-related_disorder": 4,
    "sporadic_NAFE|Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_9": 1,
    "PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases|not_provided": 3,
    "not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_9|not_provided": 1,
    "Refractory_epilepsy_with_Lennox_Gastaut_syndrome": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9|PCDH19-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Glycine_encephalopathy": 2,
    "Developmental_and_epileptic_encephalopathy|_9|Glycine_encephalopathy|not_provided": 1,
    "not_provided|PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases": 1,
    "not_provided|Glycine_encephalopathy|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Inborn_genetic_diseases|Neurodevelopmental_disorder_with_epilepsy|sporadic_NAFE|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Familial_GGE|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_specified|not_provided|PCDH19-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9|not_specified|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_9|not_provided|Glycine_encephalopathy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9|Global_developmental_delay|Bilateral_tonic-clonic_seizure|Generalized_non-motor_(absence)_seizure|Generalized-onset_seizure|Delayed_speech_and_language_development|Long_palpebral_fissure|Frontal_cortical_atrophy|Temporal_cortical_atrophy|Prominent_fingertip_pads|Strabismus|Hand_tremor": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Seizure|Inborn_genetic_diseases": 1,
    "PCDH19-related_epilepsy_syndrome|Inborn_genetic_diseases|not_provided|Epilepsy|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Developmental_and_epileptic_encephalopathy|_9|not_provided|not_specified": 1,
    "Intractable_status_epilepticus": 1,
    "Non-lesional_parietal_lobe_epilepsy|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Inborn_genetic_diseases|PCDH19-related_disorder|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_9": 1,
    "PCDH19-related_disorder|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Seizure": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases|PCDH19-related_disorder|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9|Seizure": 2,
    "developmental_delay_with_seizures|not_provided|Developmental_and_epileptic_encephalopathy|_9|Seizure": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_9|not_provided": 1,
    "Focal-onset_seizure|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Developmental_and_epileptic_encephalopathy|_9|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_9|not_specified": 1,
    "not_provided|Neurodevelopmental_disorder_with_epilepsy|not_specified|Developmental_and_epileptic_encephalopathy|_9": 1,
    "Periventricular_nodular_heterotopia_and_epilepsy": 1,
    "Neurodevelopmental_delay|Developmental_and_epileptic_encephalopathy|_9": 1,
    "PCDH19-related_epilespy": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_9|Inborn_genetic_diseases|PCDH19-related_disorder": 1,
    "Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 45,
    "not_provided|SRPX2-related_disorder": 1,
    "Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_specified": 12,
    "not_provided|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 5,
    "not_specified|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_provided": 3,
    "not_specified|not_provided|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 3,
    "not_provided|not_specified|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 1,
    "Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_specified|not_provided": 3,
    "not_provided|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_specified": 1,
    "SRPX2-related_disorder|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_provided": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|not_specified|not_provided|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 1,
    "not_specified|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 7,
    "SRPX2-related_disorder|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_specified|not_provided": 1,
    "Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|History_of_neurodevelopmental_disorder": 2,
    "Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_provided|SRPX2-related_disorder|not_specified": 1,
    "SRPX2-related_disorder": 2,
    "Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_provided": 2,
    "not_specified|SRPX2-related_disorder|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked": 1,
    "SRPX2-related_disorder|not_specified|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_provided": 1,
    "not_specified|SRPX2-related_disorder|Rolandic_epilepsy|_intellectual_disability|_and_speech_dyspraxia|_X-linked|not_provided": 1,
    "Intellectual_developmental_disorder|_X-linked_113": 1,
    "not_specified|not_provided|NOX1-related_disorder": 1,
    "NOX1-related_disorder": 4,
    "NOX1-related_disorder|not_provided": 2,
    "not_provided|Very_early_onset_inflammatory_bowel_disease": 1,
    "not_provided|DRP2-related_disorder": 5,
    "DRP2-related_disorder|not_provided": 4,
    "DRP2-related_disorder": 3,
    "Charcot-Marie-Tooth_disease|not_specified|not_provided": 1,
    "Charcot-Marie-Tooth_disease_type_X": 1,
    "Spermatogenic_failure|_X-linked|_7": 2,
    "Deafness_dystonia_syndrome": 18,
    "not_provided|Deafness_dystonia_syndrome": 1,
    "Inborn_genetic_diseases|Deafness_dystonia_syndrome": 1,
    "Deafness_dystonia_syndrome|not_provided": 2,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 25,
    "X-linked_agammaglobulinemia|Isolated_congenital_growth_hormone_deficiency": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|X-linked_agammaglobulinemia": 17,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_provided": 3,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|X-linked_agammaglobulinemia|not_provided": 5,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 471,
    "X-linked_agammaglobulinemia": 78,
    "not_provided|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 9,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_specified": 2,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_specified|not_provided": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_provided": 11,
    "not_specified|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "not_provided|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 6,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|Autosomal_recessive_agammaglobulinemia_1": 1,
    "not_provided|not_specified|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "Autosomal_recessive_agammaglobulinemia_1|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_provided": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_provided|X-linked_agammaglobulinemia|Autosomal_recessive_agammaglobulinemia_1": 1,
    "not_provided|Autosomal_recessive_agammaglobulinemia_1|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 3,
    "Autosomal_recessive_agammaglobulinemia_1|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "not_specified|Malignant_lymphoma|_large_B-cell|_diffuse|not_provided|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "not_provided|BTK-related_disorder|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "not_provided|not_specified|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|Common_variable_immunodeficiency|BTK-related_disorder": 1,
    "Inborn_genetic_diseases|not_specified|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "not_specified|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "BTK-related_disorder": 2,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|BTK-related_disorder": 1,
    "Autosomal_recessive_agammaglobulinemia_1|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|X-linked_agammaglobulinemia|not_specified|not_provided": 1,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|BTK-related_disorder": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|not_specified|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_specified": 1,
    "not_provided|BTK-related_disorder|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_specified": 1,
    "not_specified|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|BTK-related_disorder": 1,
    "not_specified|not_provided|X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|BTK-related_disorder": 2,
    "Autosomal_recessive_agammaglobulinemia_1|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|X-linked_agammaglobulinemia": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|Inherited_Immunodeficiency_Diseases": 1,
    "X-linked_agammaglobulinemia_with_growth_hormone_deficiency|X-linked_agammaglobulinemia|BTK-related_disorder": 1,
    "X-linked_agammaglobulinemia|X-linked_agammaglobulinemia_with_growth_hormone_deficiency|not_provided|not_specified": 1,
    "X-linked_agammaglobulinemia|Inherited_Immunodeficiency_Diseases|X-linked_agammaglobulinemia_with_growth_hormone_deficiency": 1,
    "BTK-related_disorder|not_provided": 1,
    "GLA-related_disorder": 10,
    "Fabry_disease|not_provided": 93,
    "Fabry_disease": 1295,
    "not_provided|Fabry_disease": 161,
    "Cardiovascular_phenotype|Fabry_disease|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|Fabry_disease": 1,
    "not_specified|Fabry_disease": 19,
    "Fabry_disease|Cardiovascular_phenotype": 31,
    "Cardiomyopathy|Fabry_disease|Cardiovascular_phenotype|GLA-related_disorder": 1,
    "not_specified|See_cases|Fabry_disease|not_provided|Hypertrophic_cardiomyopathy_1|Migalastat_response": 1,
    "Fabry_disease|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Fabry_disease|not_provided": 7,
    "Fabry_disease|Migalastat_response": 30,
    "Cardiovascular_phenotype|not_specified|not_provided|Fabry_disease": 7,
    "Fabry_disease|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|Fabry_disease|not_specified|not_provided": 1,
    "GLA-related_disorder|Fabry_disease|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|Fabry_disease": 21,
    "GLA-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Fabry_disease": 1,
    "GLA-related_disorder|not_provided|Fabry_disease": 3,
    "not_specified|Intellectual_disability|_X-linked|_syndromic|_Bain_type|not_provided|Fabry_disease|Migalastat_response": 1,
    "Cardiovascular_phenotype|not_specified|Fabry_disease": 5,
    "Fabry_disease|Primary_familial_hypertrophic_cardiomyopathy": 2,
    "Fabry_disease|Steroid-resistant_nephrotic_syndrome": 1,
    "not_specified|Fabry_disease|Cardiovascular_phenotype|not_provided": 1,
    "Fabry_disease|not_specified": 7,
    "not_specified|not_provided|Fabry_disease": 4,
    "Fabry_disease|not_specified|not_provided": 1,
    "GLA-related_disorder|Fabry_disease": 3,
    "Fabry_disease|Cardiovascular_phenotype|not_specified": 1,
    "Cardiovascular_phenotype|Fabry_disease|Migalastat_response|not_specified": 1,
    "Cardiovascular_phenotype|Fabry_disease": 22,
    "Cardiovascular_phenotype|Fabry_disease|Migalastat_response": 2,
    "Cardiovascular_phenotype|GLA-related_disorder|not_specified|not_provided|Fabry_disease": 1,
    "Cardiovascular_phenotype|Sudden_unexplained_death|not_provided|not_specified|Cardiomyopathy|Fabry_disease|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Fabry_disease|Migalastat_response|not_provided": 2,
    "Fabry_disease|not_provided|Migalastat_response": 1,
    "Cardiovascular_phenotype|not_provided|Fabry_disease|_cardiac_variant|Fabry_disease|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Fabry_disease|not_provided|not_specified": 1,
    "Fabry_disease|_cardiac_variant|Fabry_disease": 3,
    "not_provided|Fabry_disease|_cardiac_variant|Fabry_disease": 2,
    "not_specified|Fabry_disease|Cardiovascular_phenotype|not_provided|Migalastat_response|GLA-related_disorder": 1,
    "Fabry_disease|GLA-related_disorder": 3,
    "not_specified|not_provided|Fabry_disease|Migalastat_response": 1,
    "Cardiovascular_phenotype|Fabry_disease|not_specified|GLA-related_disorder": 1,
    "GLA-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Fabry_disease": 2,
    "Cardiovascular_phenotype|GLA-related_disorder|not_provided|Fabry_disease": 1,
    "Hereditary_coproporphyria|Fabry_disease": 1,
    "not_provided|Cardiovascular_phenotype|Fabry_disease": 5,
    "Cardiovascular_phenotype|Fabry_disease|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Fabry_disease|Cardiomyopathy|Hereditary_coproporphyria": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|Fabry_disease|not_provided|Cardiomyopathy": 1,
    "not_specified|not_provided|Fabry_disease|Hypertrophic_cardiomyopathy": 2,
    "Hypertrophic_cardiomyopathy|Fabry_disease|Cardiovascular_phenotype|GLA-related_disorder|not_provided|Cardiomyopathy|Fabry_disease|_cardiac_variant": 1,
    "not_specified|not_provided|Cardiomyopathy|Fabry_disease": 1,
    "GLA-related_disorder|not_specified|Fabry_disease": 1,
    "not_provided|GLA-related_disorder|not_specified|Fabry_disease": 1,
    "Cardiomyopathy|Fabry_disease": 1,
    "GLA-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Fabry_disease": 1,
    "Cardiovascular_phenotype|Fabry_disease|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|not_provided|Cardiomyopathy|Fabry_disease": 1,
    "not_provided|Fabry_disease|Migalastat_response": 3,
    "Cardiomyopathy|Cardiovascular_phenotype|Fabry_disease": 1,
    "Cardiovascular_phenotype|GLA-related_disorder|not_provided|Fabry_disease|Migalastat_response": 1,
    "RPL36A-HNRNPH2-related_disorder": 1,
    "not_provided|GLA-related_disorder|Cardiovascular_phenotype|Fabry_disease": 1,
    "Fabry_disease|Nephrotic_syndrome": 1,
    "Fabry_disease|Cardiomyopathy": 1,
    "GLA-related_disorder|Cardiovascular_phenotype|Fabry_disease": 2,
    "Cardiovascular_phenotype|Fabry_disease|Hypertrophic_cardiomyopathy|not_provided": 1,
    "Cardiovascular_phenotype|GLA-related_disorder|not_provided|not_specified|Cardiomyopathy|Fabry_disease": 1,
    "Fabry_disease|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "not_provided|Fabry_disease|not_specified": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Fabry_disease": 2,
    "not_specified|Fabry_disease|not_provided": 1,
    "Cardiovascular_phenotype|Fabry_disease|_cardiac_variant|Fabry_disease|not_provided": 1,
    "not_provided|Cardiomyopathy|Fabry_disease": 1,
    "not_provided|Fabry_disease|GLA-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|Cardiovascular_phenotype|Fabry_disease|not_provided": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Fabry_disease|Migalastat_response": 1,
    "Cardiovascular_phenotype|GLA-related_disorder|not_provided|not_specified|Fabry_disease": 1,
    "not_specified|Cardiovascular_phenotype|Fabry_disease": 2,
    "not_specified|Fabry_disease|Cardiovascular_phenotype": 1,
    "Fabry_disease|GLA-related_disorder|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Fabry_disease": 1,
    "GLA-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|Fabry_disease|Hypertrophic_cardiomyopathy": 1,
    "not_specified|Cardiomyopathy|Fabry_disease": 1,
    "GLA-related_disorder|Cardiovascular_phenotype|not_specified|Cardiomyopathy|Fabry_disease|Migalastat_response": 1,
    "Fabry_disease|Cardiovascular_phenotype|not_provided": 1,
    "GLA-related_disorder|not_specified|Cardiomyopathy|Fabry_disease": 1,
    "not_specified|Cardiomyopathy|not_provided|Fabry_disease|Hypertrophic_cardiomyopathy": 1,
    "not_provided|Fabry_disease|Hypertrophic_cardiomyopathy": 2,
    "not_provided|HNRNPH2-related_disorder": 2,
    "not_provided|Intellectual_disability|_X-linked|_syndromic|_Bain_type": 3,
    "HNRNPH2-related_disorder": 1,
    "Neurodevelopmental_disorder|Inborn_genetic_diseases|Intellectual_disability|_X-linked|_syndromic|_Bain_type|not_provided|Neurodevelopmental_delay|Stereotypic_movement_disorder|Abnormal_facial_shape": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Bain_type|HNRNPH2-related_disorder|not_provided": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Bain_type|Inborn_genetic_diseases|not_provided": 1,
    "HNRNPH2-related_disorder|not_provided": 1,
    "Intellectual_disability|_X-linked|_syndromic|_Bain_type|not_provided": 1,
    "not_provided|NXF5-related_disorder": 5,
    "NXF5-related_disorder|not_provided": 1,
    "NXF5-related_disorder": 1,
    "not_specified|ARMCX5-related_disorder": 1,
    "GPRASP1-related_disorder": 1,
    "not_specified|GPRASP1-related_disorder|not_provided": 1,
    "not_specified|GPRASP2-related_disorder": 5,
    "GPRASP2-related_disorder": 11,
    "X-linked_external_auditory_canal_atresia-dilated_internal_auditory_canal-facial_dysmorphism_syndrome": 4,
    "GPRASP2-related_disorder|not_provided": 1,
    "not_provided|GPRASP2-related_disorder": 3,
    "ARMCX5-GPRASP2-related_disorder": 1,
    "not_provided|GPRASP2-related_disorder|not_specified": 1,
    "not_provided|Deafness-intellectual_disability|_Martin-Probst_type_syndrome": 1,
    "Deafness-intellectual_disability|_Martin-Probst_type_syndrome|not_specified": 1,
    "Deafness-intellectual_disability|_Martin-Probst_type_syndrome|not_specified|not_provided": 1,
    "Neurodevelopmental_disorder_with_gait_disturbance|_dysmorphic_facies|_and_behavioral_abnormalities|_X-linked": 8,
    "Neurodevelopmental_disorder_with_gait_disturbance|_dysmorphic_facies|_and_behavioral_abnormalities|_X-linked|See_cases": 5,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|Pelizaeus-Merzbacher_disease|_mild|not_provided": 1,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2": 14,
    "Pelizaeus-Merzbacher_disease": 105,
    "Inborn_genetic_diseases|Hereditary_spastic_paraplegia_2": 1,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|Inborn_genetic_diseases": 2,
    "Hereditary_spastic_paraplegia_2|Pelizaeus-Merzbacher_disease|_mild": 1,
    "Hereditary_spastic_paraplegia_2|Inborn_genetic_diseases": 1,
    "PLP1-related_disorder": 6,
    "Pelizaeus-Merzbacher_disease|not_provided|Hereditary_spastic_paraplegia_2": 1,
    "not_specified|not_provided|Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2": 1,
    "PLP1-related_disorder|Pelizaeus-Merzbacher_disease": 1,
    "Hereditary_spastic_paraplegia_2|Inborn_genetic_diseases|not_provided": 1,
    "Pelizaeus-Merzbacher_disease|not_provided": 3,
    "Pelizaeus-Merzbacher_disease|Inborn_genetic_diseases": 1,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|PLP1-related_disorder|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Hereditary_spastic_paraplegia_2|not_provided": 10,
    "not_provided|Pelizaeus-Merzbacher_disease": 6,
    "PLP1-related_disorder|Hereditary_spastic_paraplegia_2": 1,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2": 1,
    "not_provided|Hereditary_spastic_paraplegia_2": 7,
    "Hereditary_spastic_paraplegia_2|Pelizaeus-Merzbacher_disease": 6,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|Pelizaeus-Merzbacher_disease|_atypical": 1,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2": 1,
    "not_provided|Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2": 4,
    "Pelizaeus-Merzbacher_disease|Pelizaeus-Merzbacher_disease|_atypical": 1,
    "Polycystic_kidney_disease|_adult_type|Hereditary_spastic_paraplegia_2": 1,
    "Hereditary_spastic_paraplegia_2|See_cases": 1,
    "PLP1-related_disorder|not_specified|Hereditary_spastic_paraplegia_2": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_spastic_paraplegia_2": 1,
    "Hereditary_spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia_2|Pelizaeus-Merzbacher_disease|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia_2|not_specified": 1,
    "Intellectual_disability|Pelizaeus-Merzbacher_disease": 1,
    "Pelizaeus-Merzbacher_disease|_connatal": 2,
    "Hereditary_spastic_paraplegia_2|not_provided|Pelizaeus-Merzbacher_disease": 1,
    "not_provided|Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Hereditary_spastic_paraplegia_2": 1,
    "Pelizaeus-Merzbacher_disease|Hereditary_spastic_paraplegia_2|PLP1-related_disorder": 1,
    "not_provided|H2BW1-related_disorder": 1,
    "H2BW1-related_disorder": 5,
    "not_specified|H2BW1-related_disorder": 1,
    "ESX1-related_disorder|not_provided": 1,
    "NRK-related_condition": 2,
    "Thyroxine-binding_globulin_quantitative_trait_locus": 14,
    "SERPINA7-related_disorder|not_specified|not_provided": 1,
    "Thyroxine-binding_globulin_deficiency": 1,
    "Thyroxine-binding_globulin_deficiency|_partial": 2,
    "SERPINA7-related_disorder": 2,
    "Thyroxine-binding_globulin|_Chicago": 1,
    "Thyroxine-binding_globulin_quantitative_trait_locus|SERPINA7-related_disorder|not_provided|not_specified|Thyroxine-binding_globulin|_variant_P": 1,
    "SERPINA7-related_disorder|Thyroxine-binding_globulin_deficiency|not_provided|Thyroxine-binding_globulin|_variant_A": 1,
    "Thyroxine-binding_globulin|_slow": 1,
    "not_provided|SERPINA7-related_disorder": 1,
    "RNF128-related_disorder": 1,
    "Nephrotic_syndrome|_type_20": 15,
    "not_provided|Nephrotic_syndrome|_type_20": 1,
    "TBC1D8B-related_disorder": 13,
    "not_provided|TBC1D8B-related_disorder": 6,
    "Nephrotic_syndrome|_type_20|not_specified": 3,
    "TBC1D8B-related_disorder|not_provided": 3,
    "TBC1D8B-related_disorder|not_specified|not_provided": 1,
    "Nephrotic_syndrome|_type_20|not_provided|not_specified": 1,
    "Nephrotic_syndrome|Nephrotic_syndrome|_type_20": 1,
    "not_specified|not_provided|TBC1D8B-related_disorder": 2,
    "TBC1D8B-related_disorder|not_specified": 1,
    "not_provided|Nephrotic_syndrome|_type_20|TBC1D8B-related_disorder": 1,
    "not_provided|RIPPLY1-related_disorder|not_specified": 1,
    "RIPPLY1-related_disorder": 2,
    "Azoospermia|_obstructive|_with_nephrolithiasis|Male_infertility": 1,
    "DNAAF6-related_disorder": 1,
    "Ciliary_dyskinesia|_primary|_36|_X-linked|not_provided": 2,
    "Ciliary_dyskinesia|_primary|_36|_X-linked|Inborn_genetic_diseases": 1,
    "DNAAF6-related_disorder|not_provided": 3,
    "not_provided|Ciliary_dyskinesia|_primary|_36|_X-linked|Inborn_genetic_diseases": 1,
    "not_provided|Ciliary_dyskinesia|_primary|_36|_X-linked": 1,
    "Ciliary_dyskinesia|_primary|_36|_X-linked": 5,
    "X-linked_nonsyndromic_hearing_loss|Charcot-Marie-Tooth|_X-linked|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome": 1,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_5": 5,
    "Charcot-Marie-Tooth_Neuropathy_X|Nephrolithiasis/nephrocalcinosis": 2,
    "not_specified|Charcot-Marie-Tooth_Neuropathy_X|Hearing_loss|_X-linked_1|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|Charcot-Marie-Tooth_disease_X-linked_recessive_5": 1,
    "Arts_syndrome": 7,
    "Phosphoribosylpyrophosphate_synthetase_superactivity": 7,
    "Nephrolithiasis/nephrocalcinosis|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 1,
    "not_provided|Arts_syndrome": 2,
    "Hearing_loss|_X-linked_1": 7,
    "Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Nephrolithiasis/nephrocalcinosis|Arts_syndrome|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Phosphoribosylpyrophosphate_synthetase_superactivity|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_5|Hearing_loss|_X-linked_1|Arts_syndrome|Phosphoribosylpyrophosphate_synthetase_superactivity": 2,
    "Arts_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Arts_syndrome|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Hearing_loss|_X-linked_1|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|Charcot-Marie-Tooth_disease_X-linked_recessive_5": 1,
    "Arts_syndrome|Phosphoribosylpyrophosphate_synthetase_superactivity|Inborn_genetic_diseases": 1,
    "not_provided|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_disease_X-linked_recessive_5": 1,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_5|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "not_provided|Retinal_dystrophy|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Arts_syndrome|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Phosphoribosylpyrophosphate_synthetase_superactivity|Nephrolithiasis/nephrocalcinosis|Arts_syndrome|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|not_provided|History_of_neurodevelopmental_disorder|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 1,
    "Nephrolithiasis/nephrocalcinosis|Charcot-Marie-Tooth_Neuropathy_X": 2,
    "History_of_neurodevelopmental_disorder|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|Hearing_loss|_X-linked_1|not_specified|not_provided|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "PRPS1-related_disorder|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Arts_syndrome|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Phosphoribosylpyrophosphate_synthetase_superactivity|Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided": 1,
    "Phosphoribosylpyrophosphate_synthetase_superactivity|not_provided|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Hearing_loss|_X-linked_1|Arts_syndrome|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Phosphoribosylpyrophosphate_synthetase_superactivity": 1,
    "Arts_syndrome|Phosphoribosylpyrophosphate_synthetase_superactivity": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Arts_syndrome|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Phosphoribosylpyrophosphate_synthetase_superactivity|not_specified|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "not_provided|Retinal_dystrophy|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Arts_syndrome|Phosphoribosylpyrophosphate_synthetase_superactivity|Hearing_loss|_X-linked_1": 1,
    "Retinal_dystrophy|Charcot-Marie-Tooth_Neuropathy_X|Hearing_loss|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome": 1,
    "not_specified|Arts_syndrome|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Phosphoribosylpyrophosphate_synthetase_superactivity|Charcot-Marie-Tooth_Neuropathy_X|Retinal_dystrophy": 1,
    "Retinal_dystrophy|Hearing_loss": 1,
    "Arts_syndrome|Phosphoribosylpyrophosphate_synthetase_superactivity|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_disease_X-linked_recessive_5|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "not_specified|Nephrolithiasis/nephrocalcinosis|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "PRPS1-related_disorder|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|Hearing_loss|_X-linked_1|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Arts_syndrome|Hearing_loss|_X-linked_1": 1,
    "PRPS1-related_disorder|Hearing_loss|_X-linked_1": 1,
    "Nephrolithiasis/nephrocalcinosis|Charcot-Marie-Tooth_Neuropathy_X|not_specified|not_provided": 1,
    "Arts_syndrome|Phosphoribosylpyrophosphate_synthetase_superactivity|Hearing_loss|_X-linked_1": 5,
    "Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|Hearing_loss|_X-linked_1": 5,
    "Phosphoribosylpyrophosphate_synthetase_superactivity|Hearing_loss|_X-linked_1|Arts_syndrome": 3,
    "Hearing_loss|_X-linked_1|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome": 3,
    "Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|Hearing_loss|_X-linked_1|not_provided": 2,
    "Charcot-Marie-Tooth|_X-linked|Phosphoribosylpyrophosphate_synthetase_superactivity|Arts_syndrome|X-linked_nonsyndromic_hearing_loss": 1,
    "Intellectual_disability|_X-linked_101|not_provided": 2,
    "Intellectual_disability|_X-linked_101": 12,
    "MID2-related_disorder|not_provided": 1,
    "not_provided|MID2-related_disorder": 1,
    "MID2-related_disorder": 2,
    "Intellectual_disability|_X-linked_101|not_specified": 1,
    "not_provided|MID2-related_disorder|not_specified": 1,
    "COL4A6-related_disorder|not_provided": 10,
    "not_provided|Hearing_loss|_X-linked_6|not_specified": 12,
    "Hearing_loss|_X-linked_6": 11,
    "not_specified|COL4A6-related_disorder|not_provided": 5,
    "not_specified|COL4A6-related_disorder|not_provided|Hearing_loss|_X-linked_6": 1,
    "not_provided|Hearing_loss|_X-linked_6": 17,
    "not_provided|COL4A6-related_disorder": 15,
    "not_provided|not_specified|Hearing_loss|_X-linked_6": 2,
    "COL4A6-related_disorder": 17,
    "Hearing_loss|_X-linked_6|not_provided": 8,
    "not_provided|COL4A6-related_disorder|not_specified": 1,
    "Hearing_loss|_X-linked_6|not_specified|not_provided": 2,
    "Hearing_loss|_X-linked_6|not_provided|not_specified": 2,
    "not_specified|Hearing_loss|_X-linked_6|not_provided": 1,
    "not_provided|COL4A6-related_disorder|Hearing_loss|_X-linked_6": 3,
    "COL4A6-related_disorder|not_specified|not_provided": 2,
    "not_provided|not_specified|COL4A6-related_disorder|Hearing_loss|_X-linked_6": 1,
    "COL4A6-related_disorder|not_provided|Hearing_loss|_X-linked_6": 1,
    "not_specified|COL4A6-related_disorder": 1,
    "not_provided|not_specified|COL4A6-related_disorder": 1,
    "not_provided|Lymphedema|Hearing_loss|_X-linked_6|not_specified": 1,
    "not_specified|not_provided|Hearing_loss|_X-linked_6": 1,
    "COL4A5-related_disorder|not_provided|not_specified|X-linked_Alport_syndrome": 1,
    "X-linked_Alport_syndrome|not_provided": 178,
    "not_specified|X-linked_Alport_syndrome": 1,
    "COL4A5-related_disorder|not_provided": 10,
    "not_provided|X-linked_Alport_syndrome": 152,
    "not_provided|X-linked_Alport_syndrome|COL4A5-related_disorder": 3,
    "not_provided|X-linked_Alport_syndrome|not_specified": 2,
    "COL4A5-related_disorder": 28,
    "X-linked_Alport_syndrome|COL4A5-related_disorder|not_provided": 5,
    "Inborn_genetic_diseases|not_provided|not_specified|X-linked_Alport_syndrome": 1,
    "COL4A5-related_disorder|not_specified|not_provided|X-linked_Alport_syndrome": 1,
    "X-linked_Alport_syndrome|Inborn_genetic_diseases": 6,
    "Inborn_genetic_diseases|X-linked_Alport_syndrome": 9,
    "X-linked_Alport_syndrome|COL4A5-related_disorder": 5,
    "not_specified|X-linked_Alport_syndrome|not_provided": 4,
    "X-linked_Alport_syndrome|Alport_syndrome|not_provided": 2,
    "X-linked_Alport_syndrome|not_provided|Alport_syndrome": 3,
    "Proteinuria|Hearing_impairment|Hematuria": 1,
    "COL4A5-related_disorder|not_specified|X-linked_Alport_syndrome|not_provided": 2,
    "COL4A5-related_disorder|not_provided|X-linked_Alport_syndrome": 8,
    "Alport_syndrome|X-linked_Alport_syndrome|not_provided": 1,
    "X-linked_Alport_syndrome|Disease_of_glomerular_basement_membrane|not_provided|not_specified": 1,
    "X-linked_Alport_syndrome|not_specified|not_provided": 3,
    "Inborn_genetic_diseases|not_provided|X-linked_Alport_syndrome": 3,
    "not_provided|COL4A5-related_disorder|X-linked_Alport_syndrome": 5,
    "not_provided|See_cases|X-linked_Alport_syndrome|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|X-linked_Alport_syndrome": 7,
    "Inborn_genetic_diseases|X-linked_Alport_syndrome|not_provided": 4,
    "X-linked_Alport_syndrome|not_specified": 3,
    "COL4A5-related_disorder|X-linked_Alport_syndrome|not_provided": 2,
    "COL4A5-related_disorder|X-linked_Alport_syndrome": 1,
    "Alport_syndrome|not_provided|X-linked_Alport_syndrome|COL4A5-related_disorder|Inborn_genetic_diseases": 1,
    "COL4A5-related_disorder|Inborn_genetic_diseases|not_provided|X-linked_Alport_syndrome": 2,
    "X-linked_Alport_syndrome|not_specified|Focal_segmental_glomerulosclerosis|not_provided": 1,
    "X-linked_Alport_syndrome|not_provided|COL4A5-related_disorder": 5,
    "Microscopic_hematuria|Hematuria": 1,
    "Hematuria|Kidney_damage|Downslanted_palpebral_fissures|Proteinuria": 1,
    "X-linked_Alport_syndrome|Alport_syndrome": 3,
    "not_provided|not_specified|X-linked_Alport_syndrome": 4,
    "X-linked_Alport_syndrome|Nonsyndromic_genetic_hearing_loss": 1,
    "Alport_syndrome|X-linked_Alport_syndrome": 2,
    "COL4A5-related_disorder|Alport_syndrome|not_provided|X-linked_Alport_syndrome|Hypertensive_disorder|Mild_proteinuria|Glomerulopathy": 1,
    "X-linked_Alport_syndrome|not_provided|Inborn_genetic_diseases": 3,
    "Familial_hematuria": 1,
    "not_specified|X-linked_Alport_syndrome|Atypical_hemolytic-uremic_syndrome|not_provided": 1,
    "Mild_proteinuria|Unilateral_deafness|Microscopic_hematuria": 1,
    "not_provided|COL4A5-related_disorder": 5,
    "X-linked_Alport_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|Inborn_genetic_diseases|COL4A5-related_disorder": 1,
    "X-linked_Alport_syndrome|Inborn_genetic_diseases|not_provided|COL4A5-related_disorder": 1,
    "X-linked_Alport_syndrome|Rare_genetic_deafness": 1,
    "not_provided|Atypical_hemolytic-uremic_syndrome|Alport_syndrome|Autosomal_dominant_Alport_syndrome|X-linked_Alport_syndrome": 1,
    "not_provided|X-linked_Alport_syndrome|Alport_syndrome": 1,
    "Alport_syndrome|not_provided|X-linked_Alport_syndrome": 1,
    "not_provided|COL4A5-related_disorder|Autosomal_dominant_Alport_syndrome|not_specified|X-linked_Alport_syndrome": 1,
    "Kidney_disorder|COL4A5-related_disorder|X-linked_Alport_syndrome|not_provided|not_specified": 1,
    "not_provided|X-linked_Alport_syndrome|Kidney_disorder": 1,
    "Alport_syndrome|Nephrotic_syndrome|X-linked_Alport_syndrome|not_provided": 1,
    "not_specified|COL4A5-related_disorder|X-linked_Alport_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|COL4A5-related_disorder|Hearing_impairment|not_provided|X-linked_Alport_syndrome": 1,
    "Haematuria|not_provided|X-linked_Alport_syndrome": 1,
    "not_provided|X-linked_Alport_syndrome|Rare_disease_with_thoracic_aortic_aneurysm_and_aortic_dissection|Inborn_genetic_diseases": 1,
    "X-linked_Alport_syndrome|not_specified|not_provided|Kidney_disorder": 1,
    "Alport_syndrome_1|not_provided": 1,
    "Chronic_kidney_disease|Elevated_mean_arterial_pressure|Microscopic_hematuria": 1,
    "X-linked_Alport_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|X-linked_Alport_syndrome": 1,
    "X-linked_Alport_syndrome|not_provided|not_specified": 1,
    "COL4A5-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|X-linked_Alport_syndrome": 1,
    "not_specified|not_provided|X-linked_Alport_syndrome|COL4A5-related_disorder": 1,
    "Kidney_disorder|X-linked_Alport_syndrome|not_specified|not_provided": 1,
    "not_provided|COL4A5-related_disorder|Inborn_genetic_diseases": 1,
    "X-linked_Alport_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Kidney_disorder|Inborn_genetic_diseases|not_provided|X-linked_Alport_syndrome|Hearing_impairment": 1,
    "not_provided|not_specified|Inborn_genetic_diseases|COL4A5-related_disorder": 1,
    "Proteinuria|Hematuria": 1,
    "Alport_syndrome|COL4A5-related_disorder|not_provided|X-linked_Alport_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|COL4A5-related_disorder": 1,
    "not_provided|Alport_syndrome|X-linked_Alport_syndrome": 1,
    "COL4A5-related_disorder|not_provided|Hematuria|X-linked_Alport_syndrome": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_9": 3,
    "IRS4-related_disorder": 3,
    "IRS4-related_disorder|not_specified": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_9|not_specified|not_provided": 1,
    "Hypothyroidism|_congenital|_nongoitrous|_9|not_provided": 2,
    "not_provided|Hypothyroidism|_congenital|_nongoitrous|_9": 1,
    "NXT2-related_condition": 1,
    "KCNE5-related_disorder|not_provided|Brugada_syndrome": 2,
    "Brugada_syndrome|KCNE5-related_disorder": 1,
    "not_provided|not_specified|KCNE5-related_disorder|Brugada_syndrome": 1,
    "not_provided|Intellectual_disability|_X-linked_63": 2,
    "ACSL4-related_disorder": 3,
    "Intellectual_disability|_X-linked_63": 26,
    "Non-syndromic_X-linked_intellectual_disability|not_provided|ACSL4-related_disorder|not_specified": 1,
    "Intellectual_disability|_X-linked_63|not_provided": 4,
    "Intellectual_disability|_X-linked_63|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked_63|Inborn_genetic_diseases": 1,
    "ACSL4-related_disorder|Inborn_genetic_diseases": 1,
    "ACSL4-related_disorder|Intellectual_disability|_X-linked_63|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Non-syndromic_X-linked_intellectual_disability": 1,
    "ACSL4-related_disorder|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "ACSL4-related_disorder|Intellectual_disability|_X-linked_63|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|_X-linked_63": 2,
    "not_specified|Intellectual_disability|_X-linked_63|Inborn_genetic_diseases": 1,
    "Midface_hypoplasia|_hearing_impairment|_elliptocytosis|_and_nephrocalcinosis": 8,
    "Nephrocalcinosis": 1,
    "Midface_hypoplasia|_hearing_impairment|_elliptocytosis|_and_nephrocalcinosis|not_provided": 2,
    "AMMECR1-related_disorder": 2,
    "AMMECR1-related_disorder|not_provided": 1,
    "not_specified|AMMECR1-related_disorder": 1,
    "Skraban-Deardorff_syndrome|not_specified": 1,
    "Megalocornea": 16,
    "Isolated_congenital_megalocornea": 4,
    "not_provided|CHRDL1-related_disorder": 3,
    "CHRDL1-related_disorder": 2,
    "Corneal_disorder": 1,
    "Intellectual_disability|_X-linked_30": 34,
    "Intellectual_disability|_X-linked_30|not_provided": 6,
    "not_provided|Intellectual_disability|_X-linked_30": 8,
    "Inborn_genetic_diseases|not_specified|Intellectual_disability|_X-linked_30|not_provided": 1,
    "Inborn_genetic_diseases|PAK3-related_disorder|not_provided|not_specified": 1,
    "Intellectual_disability|Intellectual_disability|_X-linked_30|not_provided": 1,
    "Congenital_anomaly_of_kidney_and_urinary_tract|Intellectual_disability|Inborn_genetic_diseases|not_provided": 1,
    "PAK3-related_disorder": 4,
    "Inborn_genetic_diseases|Intellectual_disability|_X-linked_30|PAK3-related_disorder|not_provided": 1,
    "not_specified|not_provided|History_of_neurodevelopmental_disorder|Intellectual_disability|_X-linked_30": 1,
    "Non-syndromic_X-linked_intellectual_disability|PAK3-related_disorder": 1,
    "not_provided|PAK3-related_disorder|not_specified": 1,
    "Intellectual_disability|_X-linked_30|Inborn_genetic_diseases": 2,
    "Microcephaly|Intellectual_disability": 1,
    "Intellectual_disability|_X-linked_30|Intellectual_disability": 1,
    "not_specified|Intellectual_disability|_X-linked_30|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Intellectual_disability|_X-linked_30|not_provided": 1,
    "not_provided|not_specified|Intellectual_disability|_X-linked_30|PAK3-related_disorder": 1,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation|not_provided": 3,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 25,
    "Ectopic_tissue": 61,
    "DCX-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Lissencephaly": 1,
    "Inborn_genetic_diseases|not_provided|Lissencephaly|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Ectopic_tissue": 1,
    "DCX-related_disorder": 6,
    "not_specified|Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 1,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation|not_provided|Inborn_genetic_diseases|Ectopic_tissue": 2,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Ectopic_tissue": 2,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Subcortical_laminar_heterotopia|_X-linked": 1,
    "Ectopic_tissue|not_provided": 7,
    "not_provided|Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 5,
    "Subcortical_laminar_heterotopia|_X-linked": 5,
    "not_provided|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Subcortical_laminar_heterotopia|_X-linked": 1,
    "Abnormal_cortical_gyration|not_provided": 1,
    "not_provided|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Ectopic_tissue": 4,
    "Subcortical_laminar_heterotopia|_X-linked|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Neurodevelopmental_disorder": 1,
    "not_provided|Ectopic_tissue": 6,
    "not_provided|Inborn_genetic_diseases|not_specified|DCX-related_disorder": 1,
    "Subcortical_laminar_heterotopia|_X-linked|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Abnormal_cerebral_morphology|Ectopic_tissue|not_provided|Inborn_genetic_diseases": 1,
    "Subcortical_laminar_heterotopia|_X-linked|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|Ectopic_tissue|not_provided": 1,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation|not_provided|Seizure|Ectopic_tissue": 1,
    "not_provided|Ectopic_tissue|Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 2,
    "Subcortical_laminar_heterotopia|_X-linked|Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 4,
    "Abnormal_cortical_gyration|Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 1,
    "Lissencephaly_type_1_due_to_doublecortin_gene_mutation|not_provided|Lissencephaly|Ectopic_tissue": 1,
    "not_provided|Subcortical_laminar_heterotopia|_X-linked": 1,
    "Inborn_genetic_diseases|not_provided|Lissencephaly_type_1_due_to_doublecortin_gene_mutation": 1,
    "Ectopic_tissue|Neurodevelopmental_disorder": 1,
    "Subcortical_laminar_heterotopia|_X-linked|Lissencephaly_type_1_due_to_doublecortin_gene_mutation|not_provided": 1,
    "not_provided|DCX-related_disorder|Inborn_genetic_diseases": 1,
    "ALG13-related_disorder|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_36|not_specified|Inborn_genetic_diseases": 2,
    "Developmental_and_epileptic_encephalopathy|_36|not_specified": 21,
    "Developmental_and_epileptic_encephalopathy|_36|not_provided": 49,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36": 58,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36": 7,
    "ALG13-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases": 1,
    "not_specified|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases": 15,
    "Inborn_genetic_diseases|not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|_36|not_provided|Microcephaly|Neurodevelopmental_delay|Seizure": 1,
    "not_specified|Developmental_and_epileptic_encephalopathy|_36": 18,
    "Developmental_and_epileptic_encephalopathy|_36|not_provided|Inborn_genetic_diseases": 1,
    "Developmental_and_epileptic_encephalopathy|_36|not_specified|ALG13-related_disorder": 1,
    "Rare_genetic_intellectual_disability|Inborn_genetic_diseases|Microcephaly|Neurodevelopmental_delay|Hypotonia|Seizure|ALG13-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_36|Intellectual_disability": 1,
    "Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases|not_provided": 3,
    "Developmental_and_epileptic_encephalopathy|_36|not_provided|not_specified": 2,
    "Developmental_and_epileptic_encephalopathy|_36|Hereditary_ataxia": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_36": 4,
    "not_specified|not_provided|Developmental_and_epileptic_encephalopathy|_36": 3,
    "ALG13-related_disorder|not_provided|not_specified": 1,
    "ALG13-related_disorder|Developmental_and_epileptic_encephalopathy|_36": 8,
    "not_provided|ALG13-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|_36|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|ALG13-related_disorder|not_specified|Developmental_and_epileptic_encephalopathy|_36": 1,
    "not_specified|Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_36": 2,
    "ALG13-related_disorder": 2,
    "Developmental_and_epileptic_encephalopathy|_1|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder": 3,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases|not_specified": 1,
    "Intellectual_disability|Developmental_and_epileptic_encephalopathy|_36": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|Developmental_and_epileptic_encephalopathy|_36": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_specified": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_specified": 2,
    "Congenital_disorder_of_glycosylation|Developmental_and_epileptic_encephalopathy|_1|not_specified|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|_36|not_provided|ALG13-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_36|not_specified": 1,
    "Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder|not_provided": 2,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36|Congenital_disorder_of_glycosylation": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_provided|ALG13-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36|not_specified": 1,
    "Neurodevelopmental_delay|Developmental_and_epileptic_encephalopathy|_36": 2,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36": 2,
    "not_provided|not_specified|Developmental_and_epileptic_encephalopathy|_36": 4,
    "Inborn_genetic_diseases|not_specified|not_provided|ALG13-related_disorder|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|_36|not_specified|Intellectual_disability": 1,
    "not_specified|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|Developmental_and_epileptic_encephalopathy|_36": 1,
    "not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder": 1,
    "Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder|not_specified|not_provided": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder": 2,
    "ALG13-related_disorder|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36|not_provided": 1,
    "not_specified|ALG13-related_disorder|not_provided|Inborn_genetic_diseases|Developmental_and_epileptic_encephalopathy|_36": 1,
    "not_specified|not_provided|ALG13-related_disorder|Developmental_and_epileptic_encephalopathy|_36": 1,
    "Developmental_and_epileptic_encephalopathy|_36|Developmental_and_epileptic_encephalopathy": 1,
    "Congenital_disorder_of_glycosylation|Hypotonia|Neurodevelopmental_delay|Seizure|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_36|ALG13-related_disorder|not_specified|Inborn_genetic_diseases": 1,
    "ALG13-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases|not_specified": 1,
    "ALG13-related_disorder|Developmental_and_epileptic_encephalopathy|_36|not_provided": 1,
    "Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases|not_specified": 1,
    "ALG13-related_disorder|not_provided|Developmental_and_epileptic_encephalopathy|_36": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_36|Inborn_genetic_diseases|ALG13-related_disorder": 1,
    "TRPC5-related_disorder": 93,
    "not_specified|TRPC5-related_disorder": 9,
    "TRPC5-related_disorder|not_specified": 4,
    "not_provided|TRPC5-related_disorder": 4,
    "TRPC5-related_disorder|not_provided|not_specified": 1,
    "TRPC5-related_disorder|not_provided": 3,
    "HTR2C-related_disorder": 72,
    "HTR2C-related_disorder|not_provided": 1,
    "HTR2C_POLYMORPHISM|not_provided|HTR2C-related_disorder": 1,
    "HTR2C-related_disorder|not_specified": 3,
    "not_provided|HTR2C-related_disorder": 2,
    "not_specified|HTR2C-related_disorder": 3,
    "Demyelinating_peripheral_neuropathy|Cerebellar_ataxia": 1,
    "LUZP4-related_disorder": 5,
    "Bone_mineral_density_quantitative_trait_locus_18": 9,
    "Bone_mineral_density_quantitative_trait_locus_18|not_provided": 2,
    "Bone_mineral_density_quantitative_trait_locus_18|not_specified|Osteogenesis_imperfecta|not_provided": 1,
    "not_provided|Bone_mineral_density_quantitative_trait_locus_18": 2,
    "Bone_mineral_density_quantitative_trait_locus_18|Hernia|_anterior_diaphragmatic": 1,
    "not_specified|not_provided|Bone_mineral_density_quantitative_trait_locus_18": 1,
    "Hernia|_anterior_diaphragmatic|Congenital_diaphragmatic_hernia": 2,
    "PLS3-related_disorder": 2,
    "Hernia|_anterior_diaphragmatic": 5,
    "not_provided|Osteogenesis_imperfecta|PLS3-related_disorder": 1,
    "not_provided|PLS3-related_disorder": 1,
    "PLS3-related_disorder|not_provided": 2,
    "X-linked_osteoporosis_with_fractures": 1,
    "not_provided|Inborn_genetic_diseases|PLS3-related_disorder": 1,
    "not_specified|not_provided|Intellectual_disability|_X-linked_88": 1,
    "not_provided|AGTR2-related_disorder": 2,
    "AGTR2-related_disorder|not_specified|not_provided": 2,
    "AGTR2-related_disorder": 2,
    "SLC6A14-related_disorder": 1,
    "Autoinflammatory_disease|_multisystem|_with_immune_dysregulation|_X-linked|Inborn_error_of_hematopoiesis_and_immunity_with_systemic_inflammation_and_normocytic_anemia": 2,
    "Inborn_error_of_hematopoiesis_and_immunity_with_systemic_inflammation_and_normocytic_anemia": 2,
    "DOCK11_deficiency|Autoinflammatory_disease|_multisystem|_with_immune_dysregulation|_X-linked": 5,
    "DOCK11-related_disorder": 1,
    "Autoinflammatory_disease|_multisystem|_with_immune_dysregulation|_X-linked": 4,
    "DOCK11-related_disorder|not_provided": 1,
    "DOCK11_deficiency": 2,
    "ZCCHC12-related_disorder": 1,
    "ZCCHC12-related_disorder|not_provided": 1,
    "PGRMC1-related_disorder": 1,
    "Genetic_non-acquired_premature_ovarian_failure|PGRMC1-related_disorder": 1,
    "SLC25A43-related_disorder": 3,
    "SLC25A5-related_disorder": 17,
    "Intellectual_disability|_X-linked_107": 13,
    "not_provided|Intellectual_disability|_X-linked_107": 2,
    "Syndromic_X-linked_intellectual_disability_Nascimento_type": 18,
    "not_provided|Syndromic_X-linked_intellectual_disability_Nascimento_type": 1,
    "UBE2A-related_disorder": 1,
    "Syndromic_X-linked_intellectual_disability_Nascimento_type|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Nascimento_type|Intellectual_disability": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|UBE2A-related_disorder": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_Nascimento_type|Inborn_genetic_diseases": 1,
    "SEPTIN6-related_disorder": 3,
    "UPF3B-related_disorder": 3,
    "Syndromic_X-linked_intellectual_disability_14": 156,
    "Syndromic_X-linked_intellectual_disability_14|UPF3B-related_disorder": 2,
    "not_provided|Syndromic_X-linked_intellectual_disability_14": 5,
    "Syndromic_X-linked_intellectual_disability_14|not_provided": 7,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_14": 10,
    "Syndromic_X-linked_intellectual_disability_14|Inborn_genetic_diseases": 10,
    "Syndromic_X-linked_intellectual_disability_14|not_specified|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_14": 1,
    "Syndromic_X-linked_intellectual_disability_14|UPF3B-related_disorder|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_14|not_specified": 2,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_14|not_provided": 2,
    "Syndromic_X-linked_intellectual_disability_14|Inborn_genetic_diseases|not_specified": 3,
    "Intellectual_disability|Syndromic_X-linked_intellectual_disability_14": 1,
    "UPF3B-related_disorder|Syndromic_X-linked_intellectual_disability_14": 1,
    "not_specified|Syndromic_X-linked_intellectual_disability_14": 1,
    "Syndromic_X-linked_intellectual_disability_14|Inborn_genetic_diseases|UPF3B-related_disorder|not_provided": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_14|Microcephaly|Severe_global_developmental_delay|Cataract": 1,
    "not_provided|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_14": 1,
    "Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_14|UPF3B-associated_intellectual_disability": 1,
    "UPF3B-related_disorder|Syndromic_X-linked_intellectual_disability_14|Inborn_genetic_diseases": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_14|Inborn_genetic_diseases": 1,
    "RNF113A-related_disorder|not_provided": 1,
    "RNF113A-related_disorder": 2,
    "Trichothiodystrophy_5|_nonphotosensitive": 6,
    "Trichothiodystrophy_5|_nonphotosensitive|not_provided": 3,
    "not_provided|Trichothiodystrophy_5|_nonphotosensitive": 2,
    "not_provided|RNF113A-related_disorder": 2,
    "not_specified|not_provided|RNF113A-related_disorder": 1,
    "NDUFA1-related_disorder": 1,
    "Mitochondrial_complex_I_deficiency|_nuclear_type_12": 3,
    "Mitochondrial_complex_I_deficiency|NDUFA1-related_disorder|Mitochondrial_complex_I_deficiency|_nuclear_type_12|Inborn_genetic_diseases|not_specified|not_provided|Neurofibromatosis|_type_1|Intellectual_disability": 1,
    "AKAP14-related_disorder": 1,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type": 9,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type|not_provided": 6,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type|not_provided": 1,
    "NKAP-related_disorder": 3,
    "Inborn_genetic_diseases|Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type": 1,
    "Inborn_genetic_diseases|Global_developmental_delay|Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type": 1,
    "NKAP-related_disorder|Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type|Inborn_genetic_diseases": 1,
    "Intellectual_developmental_disorder|_X-linked|_syndromic|_Hackmann-Di_Donato_type|not_provided|NKAP-related_disorder": 1,
    "NKAP-related_disorder|Inborn_genetic_diseases": 1,
    "Hypertrophic_cardiomyopathy|Danon_disease": 40,
    "Danon_disease|not_provided|Hypertrophic_cardiomyopathy": 2,
    "not_provided|Danon_disease": 26,
    "Danon_disease": 333,
    "Hypertrophic_cardiomyopathy|not_provided|Danon_disease": 11,
    "not_specified|LAMP2-related_disorder|Danon_disease|not_provided": 1,
    "not_provided|Danon_disease|Hypertrophic_cardiomyopathy|not_specified": 1,
    "Danon_disease|not_provided": 15,
    "Hypertrophic_cardiomyopathy|Danon_disease|not_provided": 5,
    "Danon_disease|Hypertrophic_cardiomyopathy|not_provided": 2,
    "not_provided|Danon_disease|Hypertrophic_cardiomyopathy": 1,
    "Cardiovascular_phenotype|Danon_disease": 25,
    "Danon_disease|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "LAMP2-related_disorder|Cardiovascular_phenotype|Danon_disease|not_specified": 1,
    "Danon_disease|Cardiovascular_phenotype": 27,
    "LAMP2-related_disorder|Cardiovascular_phenotype|not_provided|not_specified|Cardiomyopathy|Danon_disease": 1,
    "not_provided|not_specified|Danon_disease|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|Danon_disease|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|LAMP2-related_disorder|Danon_disease": 1,
    "Danon_disease|not_specified": 12,
    "not_specified|Danon_disease": 6,
    "Danon_disease|not_specified|not_provided|LAMP2-related_disorder|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "LAMP2-related_disorder|Cardiovascular_phenotype|not_specified|Danon_disease": 1,
    "Cardiovascular_phenotype|Danon_disease|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Danon_disease|not_provided": 3,
    "not_provided|Cardiovascular_phenotype|not_specified|Danon_disease": 1,
    "Primary_dilated_cardiomyopathy|Danon_disease": 1,
    "Danon_disease|Cardiovascular_phenotype|not_provided": 6,
    "Danon_disease|Cardiovascular_phenotype|not_specified": 1,
    "not_specified|Cardiovascular_phenotype|Danon_disease": 3,
    "Danon_disease|Cardiomyopathy|Cardiovascular_phenotype": 2,
    "not_specified|not_provided|Danon_disease|Trifascicular_block_on_electrocardiogram": 1,
    "LAMP2-related_disorder|Danon_disease": 1,
    "Hypertrophic_cardiomyopathy|Danon_disease|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|not_specified|Danon_disease": 1,
    "Danon_disease|not_provided|not_specified|LAMP2-related_disorder": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_provided|Danon_disease": 1,
    "not_specified|Danon_disease|Cardiovascular_phenotype": 2,
    "Danon_disease|Cardiovascular_phenotype|not_provided|not_specified": 1,
    "Danon_disease|not_provided|Cardiovascular_phenotype": 3,
    "not_specified|LAMP2-related_disorder|Cardiovascular_phenotype|Danon_disease": 1,
    "Danon_disease|Cardiomyopathy": 2,
    "not_provided|Danon_disease|Cardiovascular_phenotype": 3,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|not_specified|Danon_disease": 1,
    "Danon_disease|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "LAMP2-related_disorder|Cardiomyopathy|Danon_disease": 1,
    "not_specified|not_provided|Danon_disease": 1,
    "Isolated_Noncompaction_of_the_Ventricular_Myocardium": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Cardiomyopathy|Danon_disease|Intellectual_disability": 1,
    "Cardiovascular_phenotype|not_provided|Danon_disease": 3,
    "Hypertrophic_cardiomyopathy|Cardiovascular_phenotype|not_provided|not_specified|Danon_disease": 1,
    "Cardiomyopathy|Danon_disease": 3,
    "Hypertrophic_cardiomyopathy|Intellectual_disability|Danon_disease|not_specified|Cardiovascular_phenotype|Cardiomyopathy|not_provided": 1,
    "Danon_disease|LAMP2-related_disorder": 1,
    "Danon_disease|History_of_neurodevelopmental_disorder": 1,
    "Cardiomyopathy|Danon_disease|Cardiovascular_phenotype|not_provided": 1,
    "Danon_disease|not_specified|not_provided": 1,
    "not_specified|Danon_disease|not_provided|Cardiovascular_phenotype": 1,
    "Danon_disease|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|Cardiovascular_phenotype|Danon_disease": 1,
    "LAMP2-related_disorder|Cardiomyopathy|not_provided|Cardiovascular_phenotype|Danon_disease|not_specified": 1,
    "Cardiomyopathy|Danon_disease|not_specified|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Cardiomyopathy|not_provided|Hypertrophic_cardiomyopathy|not_specified|Danon_disease": 1,
    "LAMP2-related_disorder|not_provided|Danon_disease": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Danon_disease": 1,
    "Cardiomyopathy|Cardiovascular_phenotype|Danon_disease|not_specified": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|Danon_disease": 1,
    "Danon_disease|not_specified|Cardiovascular_phenotype": 1,
    "not_specified|Danon_disease|Primary_dilated_cardiomyopathy": 1,
    "Danon_disease|Hypertrophic_cardiomyopathy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|Danon_disease": 1,
    "Hypertrophic_cardiomyopathy|not_provided|LAMP2-related_disorder|Danon_disease|not_specified": 1,
    "Cardiovascular_phenotype|Hypertrophic_cardiomyopathy|not_specified|not_provided|Danon_disease": 1,
    "Cardiovascular_phenotype|Danon_disease|not_specified": 1,
    "Danon_disease|Primary_dilated_cardiomyopathy": 1,
    "not_specified|Cardiovascular_phenotype|Danon_disease|Cardiomyopathy": 1,
    "not_specified|Danon_disease|Cardiovascular_phenotype|not_provided": 1,
    "LAMP2-related_disorder": 3,
    "Cardiovascular_phenotype|Danon_disease|not_specified|not_provided": 1,
    "not_provided|Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Danon_disease": 1,
    "not_specified|Cardiovascular_phenotype|not_provided|Hypertrophic_cardiomyopathy|Danon_disease": 1,
    "not_specified|not_provided|LAMP2-related_disorder": 1,
    "Cardiomyopathy|Danon_disease|not_specified|not_provided|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Danon_disease|Hypertrophic_cardiomyopathy": 1,
    "X-linked_intellectual_disability_Cabezas_type": 134,
    "CUL4B-related_disorder|Inborn_genetic_diseases": 3,
    "Inborn_genetic_diseases|X-linked_intellectual_disability_Cabezas_type|not_specified": 1,
    "not_provided|CUL4B-related_disorder": 3,
    "CUL4B-related_disorder": 53,
    "X-linked_intellectual_disability_Cabezas_type|CUL4B-related_disorder": 7,
    "CUL4B-related_disorder|not_provided|not_specified|X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases": 1,
    "X-linked_intellectual_disability_Cabezas_type|not_specified": 5,
    "CUL4B-related_disorder|X-linked_intellectual_disability_Cabezas_type": 7,
    "X-linked_intellectual_disability_Cabezas_type|not_provided|not_specified": 1,
    "CUL4B-related_disorder|not_provided|Inborn_genetic_diseases|not_specified|X-linked_intellectual_disability_Cabezas_type": 1,
    "CUL4B-related_X-linked_intellectual_disability|X-linked_intellectual_disability_Cabezas_type": 1,
    "Inborn_genetic_diseases|not_provided|X-linked_intellectual_disability_Cabezas_type|not_specified": 1,
    "not_specified|CUL4B-related_disorder": 2,
    "X-linked_intellectual_disability_Cabezas_type|not_provided": 7,
    "CUL4B-related_disorder|X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|CUL4B-related_disorder": 5,
    "not_provided|X-linked_intellectual_disability_Cabezas_type": 8,
    "not_provided|Inborn_genetic_diseases|not_specified|X-linked_intellectual_disability_Cabezas_type": 1,
    "X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|X-linked_intellectual_disability_Cabezas_type": 1,
    "CUL4B-related_disorder|X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Abnormal_facial_shape|Seizure|Short_stature|Intellectual_disability|X-linked_intellectual_disability_Cabezas_type|not_provided": 1,
    "CUL4B-related_disorder|X-linked_intellectual_disability_Cabezas_type|not_provided": 1,
    "X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|X-linked_intellectual_disability_Cabezas_type": 2,
    "X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases": 1,
    "X-linked_intellectual_disability_Cabezas_type|Inborn_genetic_diseases|CUL4B-related_disorder|not_specified": 1,
    "X-linked_intellectual_disability_Cabezas_type|CUL4B-related_disorder|not_provided": 1,
    "CUL4B-related_disorder|not_provided|X-linked_intellectual_disability_Cabezas_type": 1,
    "CUL4B-related_disorder|Inborn_genetic_diseases|not_provided|X-linked_intellectual_disability_Cabezas_type": 1,
    "X-linked_intellectual_disability_Cabezas_type|Intellectual_disability": 1,
    "not_provided|CUL4B-related_disorder|not_specified": 1,
    "CUL4B-related_disorder|not_specified|not_provided|X-linked_intellectual_disability_Cabezas_type": 1,
    "X-linked_intellectual_disability_Cabezas_type|not_provided|CUL4B-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Immunodeficiency_118": 3,
    "not_specified|Polyagglutinable_erythrocyte_syndrome": 2,
    "Polyagglutinable_erythrocyte_syndrome": 23,
    "Polyagglutinable_erythrocyte_syndrome|C1GALT1C1-related_disorder": 1,
    "Hemolytic_uremic_syndrome|_atypical|_8|_with_rhizomelic_short_stature": 1,
    "not_provided|Polyagglutinable_erythrocyte_syndrome": 1,
    "Hemolytic_uremic_syndrome|_atypical|_8|_with_rhizomelic_short_stature|C1GALT1C1-related_disorder|not_provided|Polyagglutinable_erythrocyte_syndrome": 1,
    "Polyagglutinable_erythrocyte_syndrome|C1GALT1C1-related_disorder|not_provided": 1,
    "Atypical_hemolytic-uremic_syndrome|Hemolytic_uremic_syndrome|_atypical|_8|_with_rhizomelic_short_stature": 1,
    "Polyagglutinable_erythrocyte_syndrome|not_specified": 1,
    "Hemolytic_uremic_syndrome|_atypical|_8|_with_rhizomelic_short_stature|Abnormal_protein_O-linked_glycosylation": 1,
    "GLUD2-related_disorder|Parkinson_disease|_late-onset|See_cases": 1,
    "Syndromic_X-linked_intellectual_disability_94|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_94": 42,
    "not_provided|GRIA3-related_disorder": 4,
    "Syndromic_X-linked_intellectual_disability_94|not_provided": 8,
    "not_provided|Syndromic_X-linked_intellectual_disability_94": 10,
    "GRIA3-related_complex_neurodevelopmental_disorder": 2,
    "not_specified|Syndromic_X-linked_intellectual_disability_94": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_94|not_specified": 1,
    "GRIA3-related_disorder": 6,
    "GRIA3-related_disorder|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|GRIA3-related_disorder": 1,
    "Syndromic_X-linked_intellectual_disability_94|not_provided|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_94|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_94|not_provided|GRIA3-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_94|not_specified|not_provided": 1,
    "not_provided|Intellectual_disability|Syndromic_X-linked_intellectual_disability_94": 1,
    "not_specified|Syndromic_X-linked_intellectual_disability_94|not_provided": 1,
    "not_provided|See_cases|Syndromic_X-linked_intellectual_disability_94": 1,
    "Seizure|Intellectual_disability|not_provided": 1,
    "not_provided|Disrupted_sleep-wake_cycle_with_developmental_delay_and_learning_difficulty|Syndromic_X-linked_intellectual_disability_94|Inborn_genetic_diseases": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_94|Neurodevelopmental_abnormality": 1,
    "Severe_global_developmental_delay|Focal-onset_seizure|Spasticity|Generalized_hypotonia|Neurodegeneration|Infantile_spasms|Dystonic_disorder|not_provided|Epileptic_encephalopathy|Intellectual_disability": 1,
    "Neurodevelopmental_disorder|Syndromic_X-linked_intellectual_disability_94": 1,
    "X-linked_intellectual_disability-short_stature-overweight_syndrome": 43,
    "not_provided|X-linked_intellectual_disability-short_stature-overweight_syndrome": 8,
    "THOC2-related_disorder|X-linked_intellectual_disability-short_stature-overweight_syndrome": 1,
    "THOC2-related_disorder": 10,
    "X-linked_intellectual_disability-short_stature-overweight_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|THOC2-related_disorder": 1,
    "THOC2-related_disorder|not_provided": 3,
    "X-linked_intellectual_disability-short_stature-overweight_syndrome|not_provided": 5,
    "X-linked_intellectual_disability-short_stature-overweight_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|X-linked_intellectual_disability-short_stature-overweight_syndrome": 1,
    "THOC2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|THOC2-related_disorder": 1,
    "X-linked_intellectual_disability-short_stature-overweight_syndrome|THOC2-related_disorder": 1,
    "Inborn_genetic_diseases|not_provided|X-linked_intellectual_disability-short_stature-overweight_syndrome": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency": 277,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|Inborn_genetic_diseases": 4,
    "not_provided|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency": 6,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_provided": 34,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|XIAP-related_disorder": 4,
    "Inborn_genetic_diseases|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency": 7,
    "Inborn_genetic_diseases|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_provided": 1,
    "not_specified|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency": 2,
    "See_cases|not_provided|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|XIAP-related_disorder|Autoinflammatory_syndrome|not_provided": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_provided|Autoinflammatory_syndrome|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency": 1,
    "XIAP-related_disorder": 3,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|XIAP-related_disorder|not_provided": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|Autoinflammatory_syndrome": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_provided|Recurrent_infections|Sepsis": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_provided|not_specified|Autoinflammatory_syndrome": 1,
    "Autoinflammatory_syndrome|not_specified|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency": 1,
    "XIAP-related_disorder|X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_specified": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|not_specified|not_provided": 1,
    "X-linked_lymphoproliferative_disease_due_to_XIAP_deficiency|Autoinflammatory_syndrome|not_provided": 1,
    "not_provided|Lymphoproliferative_disorder": 1,
    "Mullegama-Klein-Martinez_syndrome|Holoprosencephaly_13|_X-linked|not_provided": 2,
    "not_provided|STAG2-related_disorder": 7,
    "Holoprosencephaly_13|_X-linked|Mullegama-Klein-Martinez_syndrome": 3,
    "STAG2-related_disorder": 13,
    "STAG2-related_disorder|not_provided": 3,
    "Holoprosencephaly_13|_X-linked": 6,
    "STAG2-related_disorder|Mullegama-Klein-Martinez_syndrome": 2,
    "not_provided|Mullegama-Klein-Martinez_syndrome": 4,
    "Mullegama-Klein-Martinez_syndrome|Holoprosencephaly_13|_X-linked|STAG2-related_disorder|not_provided": 1,
    "not_provided|Mullegama-Klein-Martinez_syndrome|Holoprosencephaly_13|_X-linked": 1,
    "Mullegama-Klein-Martinez_syndrome|Holoprosencephaly_13|_X-linked": 1,
    "Holoprosencephaly_13|_X-linked|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|STAG2-related_disorder": 1,
    "STAG2-related_disorder|not_provided|not_specified": 1,
    "Mullegama-Klein-Martinez_syndrome|STAG2-related_disorder": 2,
    "Mullegama-Klein-Martinez_syndrome|Inborn_genetic_diseases": 1,
    "Mullegama-Klein-Martinez_syndrome|not_provided": 2,
    "not_provided|Holoprosencephaly_13|_X-linked": 2,
    "Autoinflammatory_syndrome|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|not_provided": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|not_provided": 12,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency": 98,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|Autoinflammatory_syndrome": 1,
    "not_specified|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|Autoinflammatory_syndrome": 1,
    "X-linked_lymphoproliferative_syndrome": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|not_specified|Inborn_genetic_diseases": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|not_specified|Mullegama-Klein-Martinez_syndrome|Holoprosencephaly_13|_X-linked|not_provided": 1,
    "not_provided|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency": 2,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|Inborn_genetic_diseases": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|SH2D1A-related_disorder": 1,
    "SH2D1A-related_disorder": 1,
    "X-linked_lymphoproliferative_syndrome|not_provided|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|Lymphoproliferative_disorder|not_provided": 1,
    "SH2D1A-related_disorder|not_provided": 1,
    "Autoinflammatory_syndrome|X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|SH2D1A-related_disorder|not_provided": 1,
    "X-linked_lymphoproliferative_disease_due_to_SH2D1A_deficiency|not_specified|not_provided": 1,
    "Lymphoproliferative_disorder|not_provided": 1,
    "TENM1-related_disorder": 24,
    "TENM1-related_disorder|not_provided": 6,
    "not_provided|TENM1-related_disorder": 6,
    "not_specified|TENM1-related_disorder": 1,
    "TEX13C-related_disorder": 1,
    "ACTRT1-related_disorder|not_provided": 3,
    "not_provided|Male_infertility_with_azoospermia_or_oligozoospermia_due_to_single_gene_mutation|ACTRT1-related_disorder": 1,
    "ACTRT1-related_disorder": 2,
    "not_specified|ACTRT1-related_disorder": 1,
    "X-linked_intellectual_disability": 3,
    "SMARCA1-related_disorder": 2,
    "not_specified|SMARCA1-related_disorder": 1,
    "Lowe_syndrome|Dent_disease_type_2|Nephrolithiasis/nephrocalcinosis": 3,
    "Lowe_syndrome": 503,
    "Lowe_syndrome|Dent_disease_type_2": 41,
    "Lowe_syndrome|OCRL-related_disorder": 6,
    "not_provided|OCRL-related_disorder|Lowe_syndrome|not_specified": 1,
    "Lowe_syndrome|not_provided": 19,
    "Nephrolithiasis/nephrocalcinosis|not_specified|not_provided|Lowe_syndrome": 1,
    "not_specified|Dent_disease_type_2|Lowe_syndrome": 1,
    "not_specified|Lowe_syndrome|Nephrolithiasis/nephrocalcinosis|not_provided": 1,
    "Lowe_syndrome|Nephrolithiasis/nephrocalcinosis|not_provided|not_specified|OCRL-related_disorder": 1,
    "Nephrolithiasis/nephrocalcinosis|not_specified|Lowe_syndrome": 1,
    "Dent_disease_type_2|Lowe_syndrome|not_provided|Nephrolithiasis/nephrocalcinosis": 1,
    "Lowe_syndrome|Dent_disease_type_2|OCRL-related_disorder|Nephrolithiasis/nephrocalcinosis": 2,
    "Nephrolithiasis/nephrocalcinosis|Lowe_syndrome": 15,
    "not_provided|Lowe_syndrome": 18,
    "Lowe_syndrome|not_specified": 6,
    "not_provided|not_specified|Lowe_syndrome|Intellectual_disability|Dent_disease_type_2": 1,
    "Dent_disease_type_2|Lowe_syndrome": 4,
    "Lowe_syndrome|not_specified|not_provided": 1,
    "Lowe_syndrome|Nephrolithiasis/nephrocalcinosis|Dent_disease_type_2": 2,
    "OCRL-related_disorder": 9,
    "Lowe_syndrome|Nephrolithiasis/nephrocalcinosis": 3,
    "Congenital_myopathy|Lowe_syndrome|not_provided|OCRL-related_disorder|Nephrolithiasis/nephrocalcinosis|Dent_disease_type_2|Intellectual_disability": 1,
    "Dent_disease_type_2|Lowe_syndrome|OCRL-related_disorder|Nephrolithiasis/nephrocalcinosis": 1,
    "Nephrolithiasis/nephrocalcinosis|Genetic_developmental_and_epileptic_encephalopathy|Lowe_syndrome|Dent_disease_type_2|not_specified|not_provided|Epilepsy|Developmental_cataract": 1,
    "not_specified|not_provided|Lowe_syndrome": 1,
    "not_specified|Lowe_syndrome|Nephrolithiasis/nephrocalcinosis": 1,
    "not_provided|Lowe_syndrome|Dent_disease_type_2": 4,
    "not_specified|not_provided|Lowe_syndrome|Nephrolithiasis/nephrocalcinosis|OCRL-related_disorder": 1,
    "not_provided|Lowe_syndrome|Dent_disease_type_2|Neurodevelopmental_delay": 1,
    "not_provided|OCRL-related_disorder|Lowe_syndrome|Dent_disease_type_2": 1,
    "Lowe_syndrome|Nephrolithiasis/nephrocalcinosis|not_specified": 1,
    "not_provided|Dent_disease_type_2": 1,
    "Nephrolithiasis/nephrocalcinosis|not_provided|Lowe_syndrome": 1,
    "Lowe_syndrome|Dent_disease_type_2|not_provided": 3,
    "Nephrolithiasis/nephrocalcinosis|Lowe_syndrome|Dent_disease_type_2": 1,
    "not_specified|Lowe_syndrome|OCRL-related_disorder|Dent_disease_type_2": 1,
    "not_provided|Nephrolithiasis/nephrocalcinosis|Lowe_syndrome": 1,
    "OCRL-related_disorder|Dent_disease_type_2|Lowe_syndrome|Nephrolithiasis/nephrocalcinosis": 1,
    "Nephrolithiasis/nephrocalcinosis|Dent_disease_type_2|Lowe_syndrome": 1,
    "not_specified|Lowe_syndrome": 3,
    "Nephrolithiasis/nephrocalcinosis|not_provided|not_specified|Lowe_syndrome": 1,
    "Dent_disease_type_2|Lowe_syndrome|not_provided": 1,
    "not_provided|Lowe_syndrome|Dent_disease_type_2|Nephrolithiasis/nephrocalcinosis": 1,
    "OCRL-related_disorder|Lowe_syndrome": 1,
    "OCRL-related_disorder|Lowe_syndrome|Nephrolithiasis/nephrocalcinosis|not_specified|not_provided": 1,
    "Nephrolithiasis/nephrocalcinosis|OCRL-related_disorder|Lowe_syndrome": 1,
    "Susceptibility_to_angioedema_induced_by_ACE_inhibitors": 2,
    "Immunodeficiency_102": 5,
    "not_provided|Syndromic_X-linked_intellectual_disability_Raymond_type": 12,
    "Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Raymond_type": 5,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|not_specified|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|not_provided": 6,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|Inborn_genetic_diseases": 5,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|History_of_neurodevelopmental_disorder|not_specified|not_provided": 1,
    "not_specified|Syndromic_X-linked_intellectual_disability_Raymond_type": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_Raymond_type|Intellectual_disability|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|Autism_spectrum_disorder": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|Inborn_genetic_diseases|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|not_specified|not_provided": 1,
    "ZDHHC9-related_disorder|Syndromic_X-linked_intellectual_disability_Raymond_type": 2,
    "not_provided|Syndromic_X-linked_intellectual_disability_Raymond_type|not_specified": 1,
    "not_provided|Syndromic_X-linked_intellectual_disability_Raymond_type|Intellectual_disability": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|not_provided|ZDHHC9-related_disorder": 1,
    "not_specified|ZDHHC9-related_disorder|Syndromic_X-linked_intellectual_disability_Raymond_type": 1,
    "not_specified|not_provided|Syndromic_X-linked_intellectual_disability_Raymond_type": 1,
    "Syndromic_X-linked_intellectual_disability_Raymond_type|Inborn_genetic_diseases|See_cases": 1,
    "Shukla-Vernon_syndrome": 40,
    "Shukla-Vernon_syndrome|not_provided": 7,
    "BCORL1-related_disorder": 22,
    "not_provided|BCORL1-related_disorder": 5,
    "not_specified|Shukla-Vernon_syndrome": 4,
    "not_provided|Shukla-Vernon_syndrome": 4,
    "BCORL1-related_disorder|not_provided": 5,
    "BCORL1-related_disorder|Shukla-Vernon_syndrome|not_provided": 1,
    "not_provided|BCORL1-related_disorder|not_specified": 1,
    "Shukla-Vernon_syndrome|not_specified": 1,
    "Shukla-Vernon_syndrome|not_provided|not_specified": 1,
    "not_specified|BCORL1-related_disorder|not_provided": 1,
    "BCORL1-related_disorder|not_specified": 2,
    "not_provided|Shukla-Vernon_syndrome|BCORL1-related_disorder": 1,
    "Autoinflammatory_syndrome|_familial|_X-linked|_Behcet-like_2": 7,
    "not_provided|ELF4-related_disorder": 1,
    "ELF4-related_disorder": 2,
    "Severe_X-linked_mitochondrial_encephalomyopathy": 13,
    "not_provided|not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 139,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided": 8,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 106,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Deafness|_X-linked_5": 16,
    "Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "AIFM1-related_disorder": 8,
    "not_provided|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 6,
    "Spondyloepimetaphyseal_dysplasia|_Bieganski_type": 7,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_4|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 3,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Inborn_genetic_diseases": 4,
    "Severe_X-linked_mitochondrial_encephalomyopathy|Inborn_genetic_diseases": 1,
    "Leukodystrophy|not_provided|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_disease_X-linked_recessive_4": 1,
    "Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Severe_X-linked_mitochondrial_encephalomyopathy|AIFM1-related_disorder|not_provided": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 3,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_specified": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_disease": 2,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases": 3,
    "not_provided|not_specified|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided|AIFM1-related_disorder": 2,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type": 1,
    "Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|AIFM1-related_disorder|not_provided": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases|not_provided": 3,
    "Deafness|_X-linked_5|Inborn_genetic_diseases": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 3,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_specified|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_4": 5,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 4,
    "Deafness|_X-linked_5|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 3,
    "AIFM1-related_disorder|not_provided|Charcot-Marie-Tooth_disease|Severe_X-linked_mitochondrial_encephalomyopathy|Inborn_genetic_diseases|not_specified|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Tip-toe_gait": 1,
    "Inborn_genetic_diseases|Severe_X-linked_mitochondrial_encephalomyopathy|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Deafness|_X-linked_5|not_provided": 2,
    "AIFM1-related_disorder|Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_disease|not_specified|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Severe_X-linked_mitochondrial_encephalomyopathy": 2,
    "Deafness|_X-linked_5|Severe_X-linked_mitochondrial_encephalomyopathy|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|AIFM1-related_disorder|Deafness|_X-linked_5|not_provided|Severe_X-linked_mitochondrial_encephalomyopathy|Ear_malformation": 1,
    "not_provided|Severe_X-linked_mitochondrial_encephalomyopathy|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|AIFM1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 3,
    "not_provided|AIFM1-related_disorder|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Deafness|_X-linked_5|not_provided": 1,
    "not_specified|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 3,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease|not_specified|not_provided|Severe_X-linked_mitochondrial_encephalomyopathy": 1,
    "not_specified|Inborn_genetic_diseases|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided": 1,
    "Deafness|_X-linked_5|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Sensorineural_hearing_loss_disorder|Distal_muscle_weakness|Foot_dorsiflexor_weakness|Pes_planus|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease_X-linked_recessive_4|not_provided": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|AIFM1-related_disorder": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_disease|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Severe_X-linked_mitochondrial_encephalomyopathy|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 2,
    "Inborn_genetic_diseases|not_provided|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|AIFM1-related_disorder": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_4|Severe_X-linked_mitochondrial_encephalomyopathy": 2,
    "Charcot-Marie-Tooth_disease|not_provided|Severe_X-linked_mitochondrial_encephalomyopathy|not_specified|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Deafness|_X-linked_5": 1,
    "Inborn_genetic_diseases|not_provided|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "AIFM1-related_hypomyelination_with_spondylometaphyseal_dysplasia|Inborn_genetic_diseases|Spondyloepimetaphyseal_dysplasia|_Bieganski_type": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_specified": 2,
    "not_specified|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided|Charcot-Marie-Tooth_disease": 1,
    "not_provided|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Charcot-Marie-Tooth_disease|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease_X-linked_recessive_4|Severe_X-linked_mitochondrial_encephalomyopathy|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|AIFM1-related_disorder": 1,
    "not_provided|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_specified|Tip-toe_gait": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided|Severe_X-linked_mitochondrial_encephalomyopathy": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Prostate_cancer|not_provided": 1,
    "not_provided|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Severe_X-linked_mitochondrial_encephalomyopathy": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Severe_X-linked_mitochondrial_encephalomyopathy": 1,
    "Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided": 1,
    "Severe_X-linked_mitochondrial_encephalomyopathy|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_disease_X-linked_recessive_4": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_provided|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_disease|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X": 1,
    "Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_disease|not_provided": 1,
    "Severe_X-linked_mitochondrial_encephalomyopathy|AIFM1-related_disorder|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type": 1,
    "AIFM1-related_disorder|Inborn_genetic_diseases|Charcot-Marie-Tooth_disease": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|Autism|Inborn_genetic_diseases": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|AIFM1-related_disorder": 1,
    "Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Deafness|_X-linked_5|Severe_X-linked_mitochondrial_encephalomyopathy|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Severe_X-linked_mitochondrial_encephalomyopathy": 1,
    "not_provided|not_specified|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|Inborn_genetic_diseases": 1,
    "not_provided|Deafness|_X-linked_5|Spondyloepimetaphyseal_dysplasia|_Bieganski_type|Charcot-Marie-Tooth_disease_X-linked_recessive_4|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency|not_specified": 1,
    "Charcot-Marie-Tooth_disease|not_provided|Severe_X-linked_mitochondrial_encephalomyopathy|Charcot-Marie-Tooth_Neuropathy_X|Combined_oxidative_phosphorylation_deficiency": 1,
    "Combined_oxidative_phosphorylation_deficiency|Charcot-Marie-Tooth_Neuropathy_X|not_provided|Inborn_genetic_diseases": 1,
    "Severe_X-linked_mitochondrial_encephalomyopathy|not_provided": 2,
    "Inborn_genetic_diseases|IGSF1-related_disorder": 2,
    "IGSF1-related_disorder": 8,
    "not_specified|not_provided|X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement": 2,
    "IGSF1-related_disorder|not_provided": 2,
    "X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement": 1,
    "not_specified|IGSF1-related_disorder|not_provided": 1,
    "IGSF1-related_disorder|not_specified|not_provided": 1,
    "X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement|not_provided|not_specified": 2,
    "Inborn_genetic_diseases|not_provided|X-linked_central_congenital_hypothyroidism_with_late-onset_testicular_enlargement": 1,
    "Nystagmus_1|_congenital|_X-linked": 32,
    "Nystagmus_1|_congenital|_X-linked|not_provided": 17,
    "Infantile_Nystagmus": 1,
    "Nystagmus_1|_congenital|_X-linked|Inborn_genetic_diseases|not_provided": 3,
    "not_provided|Nystagmus_1|_congenital|_X-linked": 9,
    "Nystagmus_1|_congenital|_X-linked|not_specified|not_provided": 2,
    "not_specified|Nystagmus_1|_congenital|_X-linked|not_provided": 2,
    "Nystagmus_1|_congenital|_X-linked|Inborn_genetic_diseases": 1,
    "not_provided|FRMD7-related_disorder": 1,
    "not_provided|Nystagmus_1|_congenital|_X-linked|not_specified": 1,
    "not_provided|Nystagmus_1|_congenital|_X-linked|Inborn_genetic_diseases": 1,
    "FRMD7-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|FRMD7-related_disorder|not_provided": 1,
    "FRMD7-related_disorder": 1,
    "MBNL3-related_disorder": 3,
    "Paganini-Miozzo_syndrome": 8,
    "HS6ST2-related_disorder": 6,
    "not_specified|Paganini-Miozzo_syndrome": 1,
    "not_provided|Paganini-Miozzo_syndrome": 1,
    "not_specified|HS6ST2-related_disorder": 1,
    "Paganini-Miozzo_syndrome|not_specified": 2,
    "not_provided|HS6ST2-related_disorder": 1,
    "Spermatogenic_failure|_X-linked|_6": 2,
    "USP26-related_disorder|not_provided": 4,
    "USP26-related_disorder": 7,
    "Male_infertility|Spermatogenic_failure|_X-linked|_6": 1,
    "not_provided|USP26-related_disorder": 1,
    "GPC4-related_disorder|Keipert_syndrome": 1,
    "Keipert_syndrome": 15,
    "GPC4-related_disorder": 7,
    "not_provided|GPC4-related_disorder": 1,
    "Keipert_syndrome|not_provided": 3,
    "Distal_shortening_of_limbs": 1,
    "not_provided|Keipert_syndrome": 2,
    "Inborn_genetic_diseases|GPC4-related_disorder|not_provided": 1,
    "Keipert_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|Keipert_syndrome|not_provided": 1,
    "GPC4-related_disorder|not_provided": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1": 21,
    "not_specified|Wilms_tumor_1": 3,
    "GPC3-related_disorder|Wilms_tumor_1": 2,
    "Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1": 42,
    "Inborn_genetic_diseases|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1": 2,
    "Wilms_tumor_1|GPC3-related_disorder": 8,
    "Hereditary_cancer-predisposing_syndrome|Wilms_tumor_1": 2,
    "not_provided|Inborn_genetic_diseases|Simpson-Golabi-Behmel_syndrome_type_1": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1": 8,
    "not_provided|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_specified|not_provided|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome": 1,
    "Wilms_tumor_1|not_provided|Inborn_genetic_diseases|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|not_specified|Hereditary_cancer-predisposing_syndrome|not_provided|Simpson-Golabi-Behmel_syndrome_type_1": 1,
    "not_provided|Wilms_tumor_1|not_specified|Simpson-Golabi-Behmel_syndrome_type_1|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Wilms_tumor_1": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|not_specified|Inborn_genetic_diseases|not_provided|Wilms_tumor_1": 1,
    "GPC3-related_disorder|not_provided|Wilms_tumor_1": 2,
    "Simpson-Golabi-Behmel_syndrome_type_1|History_of_neurodevelopmental_disorder|Wilms_tumor_1": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|GPC3-related_disorder|not_provided": 1,
    "not_provided|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Inborn_genetic_diseases": 1,
    "GPC3-related_disorder|Inborn_genetic_diseases|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|not_provided": 1,
    "Hereditary_ataxia|GPC3-related_disorder|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|Intellectual_disability": 1,
    "Wilms_tumor_1|GPC3-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1": 2,
    "Wilms_tumor_1|GPC3-related_disorder|Simpson-Golabi-Behmel_syndrome_type_1": 1,
    "GPC3-related_disorder|not_provided": 1,
    "GPC3-related_disorder": 3,
    "not_provided|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1": 1,
    "Inborn_genetic_diseases|Wilms_tumor_1|not_specified|not_provided": 1,
    "GPC3-related_disorder|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|not_provided": 1,
    "not_specified|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Wilms_tumor_1": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|not_provided": 1,
    "GPC3-related_disorder|not_specified|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1": 1,
    "GPC3-related_disorder|Inborn_genetic_diseases|not_provided|Wilms_tumor_1": 2,
    "Inborn_genetic_diseases|GPC3-related_disorder|not_specified|not_provided|Wilms_tumor_1": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|Inborn_genetic_diseases|not_provided": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|GPC3-related_disorder": 1,
    "Wilms_tumor_1|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|not_provided": 1,
    "Wilms_tumor_1|Inborn_genetic_diseases|not_provided": 2,
    "Wilms_tumor_1|not_specified|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Ovarian_cancer|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|GPC3-related_disorder|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Simpson-Golabi-Behmel_syndrome_type_1": 1,
    "GPC3-related_disorder|Inborn_genetic_diseases|Hereditary_cancer-predisposing_syndrome|not_specified|not_provided|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|not_specified|Hereditary_cancer-predisposing_syndrome": 1,
    "GPC3-related_disorder|Simpson-Golabi-Behmel_syndrome_type_1|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome": 1,
    "not_provided|Wilms_tumor_1|Hereditary_cancer-predisposing_syndrome|Simpson-Golabi-Behmel_syndrome_type_1|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Hereditary_cancer-predisposing_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|Hereditary_cancer-predisposing_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|GPC3-related_disorder|Wilms_tumor_1|Simpson-Golabi-Behmel_syndrome_type_1|not_specified": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|not_provided": 1,
    "GPC3-related_disorder|Inborn_genetic_diseases|Wilms_tumor_1|not_specified|not_provided": 1,
    "Simpson-Golabi-Behmel_syndrome_type_1|not_provided|Wilms_tumor_1": 1,
    "Borjeson-Forssman-Lehmann_syndrome": 98,
    "not_provided|Hereditary_spastic_paraplegia_4|Borjeson-Forssman-Lehmann_syndrome": 1,
    "PHF6-related_disorder": 27,
    "PHF6-related_disorder|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Borjeson-Forssman-Lehmann_syndrome": 3,
    "Borjeson-Forssman-Lehmann_syndrome|not_provided": 5,
    "PHF6-related_disorder|Borjeson-Forssman-Lehmann_syndrome": 6,
    "Borjeson-Forssman-Lehmann_syndrome|not_provided|not_specified": 1,
    "not_provided|Borjeson-Forssman-Lehmann_syndrome": 6,
    "Borjeson-Forssman-Lehmann_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Borjeson-Forssman-Lehmann_syndrome|not_provided": 2,
    "not_specified|Borjeson-Forssman-Lehmann_syndrome": 1,
    "Inborn_genetic_diseases|Borjeson-Forssman-Lehmann_syndrome|PHF6-related_disorder": 1,
    "not_specified|PHF6-related_disorder|Borjeson-Forssman-Lehmann_syndrome|not_provided": 1,
    "PHF6-related_disorder|not_specified|not_provided|Borjeson-Forssman-Lehmann_syndrome": 1,
    "PHF6-related_disorder|Borjeson-Forssman-Lehmann_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Borjeson-Forssman-Lehmann_syndrome": 2,
    "PHF6-related_disorder|not_provided|Inborn_genetic_diseases|Borjeson-Forssman-Lehmann_syndrome": 2,
    "not_specified|PHF6-related_disorder": 1,
    "See_cases|Inborn_genetic_diseases|Borjeson-Forssman-Lehmann_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|PHF6-related_disorder": 1,
    "PHF6-related_disorder|not_provided": 1,
    "not_provided|PHF6-related_disorder": 2,
    "Borjeson-Forssman-Lehmann_syndrome|Inborn_genetic_diseases": 1,
    "Macrocephaly|Abnormality_of_neuronal_migration|Enlarged_cisterna_magna|Hypoplasia_of_penis|Bilateral_cryptorchidism|Rib_fusion|Horseshoe_kidney|Pulmonary_arterial_hypertension": 1,
    "not_provided|Borjeson-Forssman-Lehmann_syndrome|Intellectual_disability": 1,
    "PHF6-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "Lesch-Nyhan_syndrome": 28,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome": 83,
    "Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 47,
    "HPRT1-related_disorder|Lesch-Nyhan_syndrome": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_URANGAN": 1,
    "HPRT_CHICAGO|Lesch-Nyhan_syndrome": 1,
    "Lesch-Nyhan_syndrome|HPRT_COORPAROO": 1,
    "not_specified|not_provided|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome": 1,
    "HPRT_DETROIT|Lesch-Nyhan_syndrome": 1,
    "HPRT1-related_disorder|Lesch-Nyhan_syndrome|not_provided|Nephrolithiasis/nephrocalcinosis|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "HPRT1-related_disorder|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-nyhan_syndrome|_neurologic_variant|Lesch-Nyhan_syndrome|not_provided": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_TORONTO": 1,
    "HPRT_FUJIMI|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Microcephaly|not_provided": 1,
    "HPRT_EDINBURGH|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome": 1,
    "Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT1-related_disorder": 1,
    "HPRT1-related_disorder|HPRT_MONTREAL|Lesch-nyhan_syndrome|_neurologic_variant": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_TOOWONG": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 3,
    "not_provided|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "HPRT_NEW_HAVEN|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "HPRT_YALE|Lesch-Nyhan_syndrome|not_provided": 1,
    "HPRT_FLINT|Lesch-Nyhan_syndrome": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_SWAN": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_ARLINGTON|Lesch-Nyhan_syndrome": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_MUNICH": 1,
    "Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|not_provided|not_specified": 1,
    "Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|not_provided": 2,
    "HPRT1-related_disorder": 3,
    "Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|not_specified": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome|History_of_neurodevelopmental_disorder|not_specified": 1,
    "Lesch-Nyhan_syndrome|not_provided|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "HPRT_LONDON|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome|not_provided": 3,
    "not_specified|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome": 1,
    "HPRT_MIDLAND|Lesch-Nyhan_syndrome": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_ANN_ARBOR": 1,
    "HPRT_TOKYO|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "not_provided|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome": 2,
    "HPRT_PARIS|Lesch-Nyhan_syndrome": 1,
    "Nephrolithiasis/nephrocalcinosis|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|not_specified": 1,
    "HPRT_MILWAUKEE|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|Lesch-Nyhan_syndrome": 1,
    "HPRT_CHERMSIDE|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "Nephrolithiasis/nephrocalcinosis|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "HPRT_MICHIGAN|Lesch-Nyhan_syndrome": 1,
    "not_provided|Lesch-Nyhan_syndrome": 1,
    "HPRT1-related_disorder|Lesch-Nyhan_syndrome|Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_MOOSE_JAW": 1,
    "HPRT_NEW_BRITON|Lesch-Nyhan_syndrome": 1,
    "Partial_hypoxanthine-guanine_phosphoribosyltransferase_deficiency|HPRT_ASHVILLE": 1,
    "Lesch-Nyhan_syndrome|HPRT1-related_disorder|not_provided": 1,
    "HPRT_EVANSVILLE|Lesch-Nyhan_syndrome": 1,
    "SAGE1-related_disorder": 18,
    "not_provided|SAGE1-related_disorder": 1,
    "not_specified|SAGE1-related_disorder": 1,
    "not_specified|SLC9A6-related_disorder": 1,
    "not_provided|not_specified|Christianson_syndrome": 3,
    "Christianson_syndrome|Neurodevelopmental_disorder|not_provided": 1,
    "Inborn_genetic_diseases|Christianson_syndrome|not_provided": 2,
    "Christianson_syndrome|not_provided": 25,
    "Christianson_syndrome|SLC9A6-related_disorder": 3,
    "Christianson_syndrome": 287,
    "not_provided|Christianson_syndrome": 43,
    "Inborn_genetic_diseases|not_provided|not_specified|Obesity|Christianson_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|Christianson_syndrome": 3,
    "not_specified|Christianson_syndrome": 9,
    "SLC9A6-related_disorder|Christianson_syndrome": 1,
    "not_provided|Inborn_genetic_diseases|Christianson_syndrome": 2,
    "Christianson_syndrome|not_specified|not_provided": 1,
    "SLC9A6-related_disorder|not_provided|Christianson_syndrome|Inborn_genetic_diseases": 1,
    "Christianson_syndrome|not_specified": 12,
    "SLC9A6-related_disorder": 4,
    "Christianson_syndrome|Inborn_genetic_diseases": 7,
    "not_specified|not_provided|Christianson_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|Christianson_syndrome|Intellectual_disability": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Christianson_syndrome": 1,
    "Christianson_syndrome|SLC9A6-related_disorder|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "Christianson_syndrome|Inborn_genetic_diseases|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|Intellectual_disability|Christianson_syndrome": 1,
    "not_specified|Christianson_syndrome|Inborn_genetic_diseases": 1,
    "Christianson_syndrome|Intellectual_disability": 1,
    "Christianson_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "SLC9A6-related_disorder|History_of_neurodevelopmental_disorder|not_provided|Christianson_syndrome": 1,
    "not_provided|Christianson_syndrome|Global_developmental_delay|Seizure|Sleep_abnormality|Scoliosis|Gastrostomy_tube_feeding_in_infancy|Recurrent_respiratory_infections": 1,
    "Astigmatism|Allergy|Strabismus|Amblyopia|Delayed_speech_and_language_development|Motor_delay|Seizure|Short_stature|EEG_with_generalized_slow_activity|Open_mouth|Hypermetropia|Microcephaly|Leukodystrophy": 1,
    "Inborn_genetic_diseases|Christianson_syndrome|not_specified|not_provided": 1,
    "SLC9A6-related_disorder|not_specified|Christianson_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Christianson_syndrome|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Christianson_syndrome|Intellectual_disability": 1,
    "Christianson_syndrome|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|Christianson_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|Christianson_syndrome|not_specified|Inborn_genetic_diseases": 1,
    "Christianson_syndrome|History_of_neurodevelopmental_disorder|Intellectual_disability|not_specified": 1,
    "not_provided|X-linked_scapuloperoneal_muscular_dystrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "FHL1-related_disorder|not_provided": 1,
    "FHL1-related_disorder": 4,
    "Uruguay_Faciocardiomusculoskeletal_syndrome": 3,
    "FHL1-related_disorder|not_specified": 1,
    "X-linked_scapuloperoneal_muscular_dystrophy": 2,
    "X-linked_myopathy_with_postural_muscle_atrophy": 247,
    "X-linked_myopathy_with_postural_muscle_atrophy|Cardiovascular_phenotype|not_provided": 3,
    "X-linked_myopathy_with_postural_muscle_atrophy|Cardiovascular_phenotype": 23,
    "X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|not_provided": 1,
    "Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy": 25,
    "not_provided|X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_scapuloperoneal_muscular_dystrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|Cardiovascular_phenotype": 1,
    "not_provided|X-linked_myopathy_with_postural_muscle_atrophy|Cardiovascular_phenotype": 6,
    "not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 19,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|FHL1-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|Cardiovascular_phenotype": 6,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided": 14,
    "Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy|not_provided": 4,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_specified": 3,
    "X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe": 1,
    "Cardiovascular_phenotype|Familial_hemophagocytic_lymphohistiocytosis_type_1|not_provided|not_specified|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "not_specified|X-linked_myopathy_with_postural_muscle_atrophy": 11,
    "not_specified|not_provided|X-linked_myopathy_with_postural_muscle_atrophy|Cardiovascular_phenotype": 2,
    "Cardiovascular_phenotype|not_provided|X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|FHL1-related_disorder|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|X-linked_scapuloperoneal_muscular_dystrophy|X-linked_myopathy_with_postural_muscle_atrophy|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy": 3,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|Cardiovascular_phenotype|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe": 1,
    "not_provided|X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset|Cardiovascular_phenotype": 1,
    "X-linked_cardiomyopathies|X-linked_myopathies|X-linked_myopathy_with_postural_muscle_atrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|FHL1-related_disorder|not_specified|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_childhood-onset": 3,
    "Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy|not_provided|Cardiovascular_phenotype": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|FHL1-related_disorder|Cardiovascular_phenotype": 1,
    "X-linked_scapuloperoneal_muscular_dystrophy|not_provided": 1,
    "Myopathy|_reducing_body|_X-linked|_early-onset|_severe": 4,
    "X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "Centronuclear_myopathy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe": 1,
    "Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Uruguay_Faciocardiomusculoskeletal_syndrome|Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_scapuloperoneal_muscular_dystrophy|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_type_1|not_specified|Cardiovascular_phenotype|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|FHL1-related_disorder|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "Abnormality_of_the_musculature|Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "FHL1-related_disorder|Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy|not_provided": 1,
    "FHL1-related_disorder|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "not_specified|not_provided|Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_type_1|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Uruguay_Faciocardiomusculoskeletal_syndrome": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_specified|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|Cardiovascular_phenotype|X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Uruguay_Faciocardiomusculoskeletal_syndrome": 1,
    "Emery-Dreifuss_muscular_dystrophy_6|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "X-linked_scapuloperoneal_muscular_dystrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome": 1,
    "Asymmetric_septal_hypertrophy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_specified|not_provided": 2,
    "FHL1-related_disorder|not_specified|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|not_specified": 1,
    "FHL1-related_disorder|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "not_provided|not_specified|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "not_specified|FHL1-related_disorder|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "not_specified|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|not_provided|not_specified|Cardiovascular_phenotype": 1,
    "Familial_hemophagocytic_lymphohistiocytosis_type_1": 1,
    "not_specified|X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|not_provided|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|FHL1-related_disorder|not_provided|not_specified|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|X-linked_myopathy_with_postural_muscle_atrophy|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy|not_specified": 1,
    "X-linked_scapuloperoneal_muscular_dystrophy|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Myopathy|_reducing_body|_X-linked|_childhood-onset|X-linked_scapuloperoneal_muscular_dystrophy|Uruguay_Faciocardiomusculoskeletal_syndrome": 1,
    "Cardiovascular_phenotype|not_provided|X-linked_myopathy_with_postural_muscle_atrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "X-linked_myopathy_with_postural_muscle_atrophy|FHL1-related_disorder|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 2,
    "Cardiovascular_phenotype|X-linked_myopathy_with_postural_muscle_atrophy|Myopathy|_reducing_body|_X-linked|_childhood-onset|Myopathy|_reducing_body|_X-linked|_early-onset|_severe|Uruguay_Faciocardiomusculoskeletal_syndrome|X-linked_scapuloperoneal_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_6": 2,
    "Cardiovascular_phenotype|not_specified|not_provided|X-linked_myopathy_with_postural_muscle_atrophy": 1,
    "MAP7D3-related_disorder": 8,
    "MAP7D3-related_disorder|not_provided": 2,
    "not_provided|MAP7D3-related_disorder": 1,
    "ADGRG4-related_disorder": 8,
    "not_specified|ADGRG4-related_disorder": 1,
    "not_provided|ADGRG4-related_disorder": 1,
    "HTATSF1-related_disorder|not_specified": 1,
    "not_specified|not_provided|Hyper-IgM_syndrome_type_1": 1,
    "CD40LG-related_disorder": 2,
    "Hyper-IgM_syndrome_type_1": 222,
    "Hyper-IgM_syndrome_type_1|not_specified|not_provided": 1,
    "Hyper-IgM_syndrome_type_1|not_provided": 15,
    "Hyper-IgM_syndrome_type_1|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Hyper-IgM_syndrome_type_1|not_provided": 1,
    "Hyper-IgM_syndrome_type_1|Inborn_genetic_diseases": 5,
    "not_provided|Hyper-IgM_syndrome_type_1": 4,
    "Hyper-IgM_syndrome_type_1|Common_variable_immunodeficiency": 1,
    "CD40LG-related_disorder|Hyper-IgM_syndrome_type_1": 2,
    "not_provided|Hyper-IgM_syndrome_type_1|not_specified": 1,
    "Hyper-IgM_syndrome_type_1|not_specified": 1,
    "not_specified|Hyper-IgM_syndrome_type_1": 1,
    "Inborn_genetic_diseases|Hyper-IgM_syndrome_type_1": 2,
    "not_provided|not_specified|Hyper-IgM_syndrome_type_1": 1,
    "not_provided|Hyper-IgM_syndrome_type_1|CD40LG-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Hyper-IgM_syndrome_type_1": 1,
    "not_provided|ARHGEF6-related_disorder": 1,
    "ARHGEF6-related_disorder": 4,
    "ARHGEF6-related_disorder|not_provided": 1,
    "not_specified|Intellectual_disability|_X-linked_46": 1,
    "not_specified|ARHGEF6-related_disorder|not_provided": 2,
    "not_provided|ARHGEF6-associated_Neurodevelopmental_disorder|Intellectual_disability|_X-linked_46": 1,
    "Intellectual_disability|_X-linked_46": 1,
    "ARHGEF6-related_disorder|not_provided|not_specified": 1,
    "ARHGEF6-related_disorder|not_specified": 1,
    "Non-syndromic_X-linked_intellectual_disability|not_specified|not_provided|ARHGEF6-related_disorder": 1,
    "Genetic_developmental_and_epileptic_encephalopathy|ARHGEF6-related_disorder|not_specified|not_provided|Intellectual_disability|_X-linked_46|Intellectual_disability": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Intellectual_disability|_X-linked_46": 1,
    "not_provided|ARHGEF6-related_disorder|Intellectual_disability|_X-linked_46": 1,
    "RBMX-related_disorder": 3,
    "Severe_X-linked_intellectual_disability|_Gustavson_type": 3,
    "Syndromic_X-linked_intellectual_disability_Shashi_type|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_Shashi_type|not_provided": 1,
    "not_specified|Pituitary_adenoma|_growth_hormone-secreting|_2|X-linked_acrogigantism_due_to_Xq26_microduplication": 1,
    "not_provided|GPR101-related_disorder": 1,
    "Pituitary_adenoma|_growth_hormone-secreting|_2": 1,
    "not_provided|GPR101-related_disorder|Pituitary_adenoma|_growth_hormone-secreting|_2": 1,
    "not_provided|GPR101-related_disorder|not_specified": 1,
    "GPR101-related_disorder|not_provided|not_specified": 1,
    "Pituitary_adenoma|_growth_hormone-secreting|_2|X-linked_acrogigantism_due_to_Xq26_microduplication": 1,
    "Heterotaxy|_visceral|_1|_X-linked|not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Congenital_heart_defects_1|_nonsyndromic|_1": 1,
    "Heterotaxy|_visceral|_1|_X-linked|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 13,
    "Heterotaxy|_visceral|_1|_X-linked": 68,
    "Heterotaxy|_visceral|_1|_X-linked|not_provided": 3,
    "Congenital_heart_defects_1|_nonsyndromic|_1|not_provided|not_specified|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Heterotaxy|_visceral|_1|_X-linked": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 2,
    "ZIC3-related_disorder": 11,
    "Inborn_genetic_diseases|Heterotaxy|_visceral|_1|_X-linked": 1,
    "not_provided|Heterotaxy|_visceral|_1|_X-linked": 5,
    "Congenital_heart_defects_1|_nonsyndromic|_1|Inborn_genetic_diseases|Heterotaxy|_visceral|_1|_X-linked|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 1,
    "not_specified|not_provided|Heterotaxy|_visceral|_1|_X-linked|ZIC3-related_disorder": 1,
    "ZIC3-related_disorder|Heterotaxy|_visceral|_1|_X-linked": 1,
    "Heterotaxy|_visceral|_1|_X-linked|ZIC3-related_disorder": 1,
    "not_provided|Heterotaxy|_visceral|_1|_X-linked|ZIC3-related_disorder": 1,
    "not_provided|Heterotaxy|_visceral|_1|_X-linked|not_specified": 1,
    "Heterotaxy|_visceral|_1|_X-linked|not_provided|ZIC3-related_disorder": 1,
    "Heterotaxy|_visceral|_1|_X-linked|not_provided|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|ZIC3-related_disorder": 1,
    "Heterotaxy|_visceral|_1|_X-linked|not_specified": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Congenital_heart_defects|_multiple_types|_1|_X-linked|Heterotaxy|_visceral|_1|_X-linked|not_provided|Congenital_heart_defects_1|_nonsyndromic|_1|not_specified": 1,
    "Heterotaxy|_visceral|_1|_X-linked|Inborn_genetic_diseases": 1,
    "Heterotaxy|_visceral|_1|_X-linked|not_specified|not_provided": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Congenital_heart_defects_1|_nonsyndromic|_1|Heterotaxy|_visceral|_1|_X-linked": 3,
    "not_specified|not_provided|Heterotaxy|_visceral|_1|_X-linked": 1,
    "VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Heterotaxy|_visceral|_1|_X-linked": 1,
    "Congenital_heart_defects|_multiple_types|_1|_X-linked": 1,
    "ZIC3-related_disorder|Inborn_genetic_diseases|Heterotaxy|_visceral|_1|_X-linked": 1,
    "Congenital_heart_defects_1|_nonsyndromic|_1|Heterotaxy|_visceral|_1|_X-linked|VACTERL_association|_X-linked|_with_or_without_hydrocephalus": 6,
    "Heterotaxy|_visceral|_1|_X-linked|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|not_provided": 1,
    "Congenital_heart_defects_1|_nonsyndromic|_1|VACTERL_association|_X-linked|_with_or_without_hydrocephalus|Heterotaxy|_visceral|_1|_X-linked": 1,
    "Developmental_and_epileptic_encephalopathy|_90": 9,
    "not_provided|Inborn_genetic_diseases|FGF13-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_90|not_provided": 2,
    "FGF13-related_disorder": 1,
    "not_provided|Developmental_and_epileptic_encephalopathy|_90": 1,
    "not_provided|FGF13-related_disorder": 1,
    "Developmental_and_epileptic_encephalopathy|_90|FGF13-related_disorder": 1,
    "Intellectual_developmental_disorder|_X-linked_110|Developmental_and_epileptic_encephalopathy|_90": 1,
    "Intellectual_developmental_disorder|_X-linked_110": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 166,
    "HEMOPHILIA_B_BRANDENBURG": 1,
    "Hemophilia_B_leyden": 4,
    "Hemophilia_B_leyden|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease": 115,
    "not_provided|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Hemophilia_B_leyden": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked|not_provided|F9-related_disorder|not_specified": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked|not_provided|F9_POLYMORPHISM|F9-related_disorder": 1,
    "F9-related_disorder": 11,
    "Hereditary_factor_IX_deficiency_disease": 151,
    "Hereditary_factor_IX_deficiency_disease|not_specified": 6,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_provided": 7,
    "not_provided|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 3,
    "Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease": 10,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked": 1,
    "Warfarin_sensitivity|_X-linked": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_specified|not_provided": 2,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|not_provided|not_specified": 1,
    "F9-related_disorder|not_provided": 1,
    "Warfarin_sensitivity|_X-linked|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 2,
    "not_specified|Hereditary_factor_IX_deficiency_disease": 8,
    "Hereditary_factor_IX_deficiency_disease|not_provided": 3,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|Hereditary_factor_VIII_deficiency_disease|not_provided": 1,
    "Reduced_factor_IX_activity": 1,
    "not_provided|Hereditary_factor_IX_deficiency_disease": 5,
    "Hereditary_factor_IX_deficiency_disease|not_provided|Warfarin_sensitivity|_X-linked|Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked|Thrombophilia|_X-linked|_due_to_factor_9_defect": 2,
    "F9-related_disorder|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|not_provided": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|not_specified": 3,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_specified": 1,
    "not_specified|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 2,
    "not_specified|Warfarin_sensitivity|_X-linked|Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|not_provided": 2,
    "Hereditary_factor_IX_deficiency_disease|not_specified|Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "Hereditary_factor_VIII_deficiency_disease|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 2,
    "not_provided|Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|not_provided": 2,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "Deep_venous_thrombosis|_protection_against|Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|not_specified|not_provided": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|F9-related_disorder": 1,
    "F9-related_disorder|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_provided": 1,
    "F9-related_disorder|Hemophilia_b(m)|not_provided|Hereditary_factor_IX_deficiency_disease": 1,
    "Hemophilia_b(m)": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|F9-related_disorder": 2,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|F9-related_disorder": 1,
    "F9-related_disorder|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|FACTOR_IX|_DNA_POLYMORPHISM|not_provided": 1,
    "not_provided|Abnormality_of_coagulation|Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease": 1,
    "not_provided|Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease": 2,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "not_specified|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_provided": 1,
    "not_provided|Hereditary_factor_VIII_deficiency_disease|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "not_specified|Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|not_specified": 1,
    "F9-related_disorder|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|not_specified|FACTOR_IX_POLYMORPHISM": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|not_specified|not_provided": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked|F9-related_disorder|not_specified|not_provided": 1,
    "F9-related_disorder|not_provided|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked|Hereditary_factor_VIII_deficiency_disease": 1,
    "F9-related_disorder|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect": 3,
    "not_specified|Abnormality_of_coagulation": 1,
    "Hereditary_factor_IX_deficiency_disease|not_provided|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_specified": 1,
    "Hereditary_factor_IX_deficiency_disease|not_specified|not_provided|Thrombophilia|_X-linked|_due_to_factor_9_defect|F9-related_disorder": 1,
    "haemophilia_B": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_provided|not_specified": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_specified|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "F9-related_disorder|Hereditary_factor_IX_deficiency_disease|not_specified|Thrombophilia|_X-linked|_due_to_factor_9_defect": 1,
    "Thrombus|Inborn_genetic_diseases": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked|not_specified": 1,
    "not_specified|Hereditary_factor_IX_deficiency_disease|not_provided": 1,
    "not_provided|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_provided|Warfarin_sensitivity|_X-linked|Hereditary_factor_VIII_deficiency_disease|F9-related_disorder": 1,
    "not_specified|Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Warfarin_sensitivity|_X-linked": 1,
    "Thrombophilia|_X-linked|_due_to_factor_9_defect|Hereditary_factor_IX_deficiency_disease|Inborn_genetic_diseases": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|Warfarin_sensitivity|_X-linked": 1,
    "Hemophilia_B|_Factor_IX_Deficiency": 5,
    "Hereditary_factor_VIII_deficiency_disease|Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_9_defect|not_provided": 1,
    "Hypotonia|Failure_to_thrive": 1,
    "ATP11C-related_disorder": 4,
    "X-linked_congenital_hemolytic_anemia": 5,
    "ATP11C-related_disorder|not_provided": 2,
    "ATP11C-related_disorder|not_specified|not_provided": 1,
    "not_provided|ATP11C-related_disorder": 1,
    "SOX3-related_disorder": 9,
    "Panhypopituitarism|_X-linked": 2,
    "Intellectual_disability|_X-linked|_with_panhypopituitarism": 4,
    "SOX3-related_disorder|not_provided": 3,
    "SOX3-related_disorder|Intellectual_disability|_X-linked|_with_panhypopituitarism|Panhypopituitarism|_X-linked|not_specified|not_provided": 1,
    "Panhypopituitarism|_X-linked|History_of_neurodevelopmental_disorder|not_provided": 1,
    "X-linked_intellectual_disability_with_isolated_growth_hormone_deficiency": 1,
    "SOX3-related_disorder|not_provided|Intellectual_disability|_X-linked|_with_panhypopituitarism": 1,
    "SOX3-related_disorder|not_specified": 1,
    "Intellectual_disability|_X-linked|_with_panhypopituitarism|Panhypopituitarism|_X-linked|not_provided": 1,
    "SOX3-related_disorder|Panhypopituitarism|_X-linked|Intellectual_disability|_X-linked|_with_panhypopituitarism|not_specified|not_provided": 1,
    "SOX3-related_disorder|not_specified|not_provided": 1,
    "Intellectual_disability|_X-linked|_with_panhypopituitarism|not_specified": 2,
    "Intellectual_disability|_X-linked|_with_panhypopituitarism|Panhypopituitarism|_X-linked": 1,
    "not_provided|Panhypopituitarism|_X-linked": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Intellectual_disability|_X-linked|_with_panhypopituitarism|Abnormal_brain_morphology": 1,
    "See_cases|Oligospermia|Abnormal_sperm_morphology": 1,
    "Intellectual_disability|_X-linked|_with_panhypopituitarism|not_provided": 1,
    "not_specified|SOX3-related_disorder|not_provided|Panhypopituitarism|_X-linked|Intellectual_disability|_X-linked|_with_panhypopituitarism": 1,
    "MAGEC3-related_disorder": 1,
    "Intellectual_developmental_disorder|_X-linked_111": 9,
    "Intellectual_developmental_disorder|_X-linked_111|not_specified": 1,
    "Intellectual_disability|Intellectual_developmental_disorder|_X-linked_111": 2,
    "Intellectual_developmental_disorder|_X-linked_111|Intellectual_disability": 4,
    "Intellectual_developmental_disorder|_X-linked_111|not_provided": 1,
    "SLITRK2-related_condition|not_provided": 1,
    "Fragile_X_syndrome": 18,
    "Fragile_X_syndrome|Fragile_X-associated_tremor/ataxia_syndrome|Premature_ovarian_failure_1|not_provided|not_specified": 1,
    "not_provided|Fragile_X_syndrome": 1,
    "not_provided|not_specified|FMR1-related_disorder|Inborn_genetic_diseases|Fragile_X-associated_tremor/ataxia_syndrome|Fragile_X_syndrome|Premature_ovarian_failure_1": 1,
    "Fragile_X_syndrome|Premature_ovarian_failure_1|Fragile_X-associated_tremor/ataxia_syndrome|not_provided": 1,
    "Fragile_X_syndrome|Fragile_X-associated_tremor/ataxia_syndrome|Premature_ovarian_failure_1|not_specified|not_provided|Inborn_genetic_diseases": 1,
    "FMR1-related_disorder": 4,
    "not_provided|FMR1-related_disorder": 2,
    "Inborn_genetic_diseases|not_specified|Fragile_X_syndrome|Premature_ovarian_failure_1|Fragile_X-associated_tremor/ataxia_syndrome|not_provided": 1,
    "not_specified|FMR1-related_disorder|not_provided": 1,
    "Fragile_X_syndrome|not_specified|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Fragile_X_syndrome|not_provided": 2,
    "FMR1-related_disorder|Inborn_genetic_diseases|not_provided|Fragile_X_syndrome|not_specified": 1,
    "Fragile_X_syndrome|Premature_ovarian_failure_1|Fragile_X-associated_tremor/ataxia_syndrome|Inborn_genetic_diseases": 1,
    "Fragile_X-associated_tremor/ataxia_syndrome": 1,
    "Fragile_X_syndrome|FMR1-related_disorder|not_provided": 1,
    "FRAXE": 35,
    "AFF2-related_disorder|not_specified": 1,
    "FRAXE|not_provided": 8,
    "AFF2-related_disorder": 9,
    "not_provided|FRAXE": 4,
    "Inborn_genetic_diseases|AFF2-related_disorder|not_provided": 1,
    "not_specified|AFF2-related_disorder|not_provided": 1,
    "AFF2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|not_provided|FRAXE": 1,
    "not_provided|AFF2-related_disorder|not_specified": 1,
    "not_specified|FRAXE": 1,
    "AFF2-related_disorder|Non-syndromic_X-linked_intellectual_disability|not_provided|not_specified": 1,
    "AFF2-related_disorder|not_provided": 2,
    "FRAXE|Inborn_genetic_diseases|not_provided": 1,
    "AFF2-related_disorder|not_specified|not_provided|FRAXE|Intellectual_disability": 1,
    "AFF2-related_disorder|not_specified|not_provided|FRAXE": 1,
    "FRAXE|Inborn_genetic_diseases": 2,
    "AFF2-related_disorder|not_provided|FRAXE|Intellectual_disability": 1,
    "Synophrys|Primary_microcephaly|Hypotonia|Hirsutism|Intellectual_disability|_moderate|Short_stature|Myopia|Inborn_genetic_diseases": 1,
    "FRAXE|not_provided|not_specified": 1,
    "not_specified|not_provided|AFF2-related_disorder": 1,
    "IDS-related_disorder": 6,
    "Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A": 8,
    "Mucopolysaccharidosis|_MPS-II|IDS-related_disorder": 2,
    "Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases": 16,
    "not_provided|Mucopolysaccharidosis|_MPS-II": 25,
    "Mucopolysaccharidosis|_MPS-II|not_provided": 27,
    "not_specified|Mucopolysaccharidosis|_MPS-II": 5,
    "Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-II|not_provided": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II": 10,
    "Mucopolysaccharidosis_type_2|_severe_form|Mucopolysaccharidosis|_MPS-II": 1,
    "not_provided|Mucopolysaccharidosis_type_2|_severe_form|Mucopolysaccharidosis|_MPS-II": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_type_II|_mild_form": 1,
    "Mucopolysaccharidosis|_MPS-II|not_specified|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-II|See_cases|Mucopolysaccharidosis|_MPS-III-A|not_provided": 1,
    "IDS-related_disorder|Epidermolysis_bullosa_simplex_with_nail_dystrophy|Mucopolysaccharidosis|_MPS-II": 1,
    "Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A": 4,
    "Mucopolysaccharidosis|_MPS-II|not_provided|Inborn_genetic_diseases": 2,
    "Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Mucopolysaccharidosis|_MPS-II": 3,
    "Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A": 3,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A": 3,
    "IDS-related_disorder|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|not_provided": 1,
    "Mucopolysaccharidosis|_type_II|_mild_form|Mucopolysaccharidosis|_MPS-II": 1,
    "Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|not_provided": 3,
    "Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II": 7,
    "Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II|IDS-related_disorder": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A": 2,
    "Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|not_specified": 1,
    "Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A|IDS-related_disorder|not_specified|not_provided": 1,
    "IDS-related_disorder|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II|not_specified|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Mucopolysaccharidosis|_MPS-III-A|not_provided|Mucopolysaccharidosis|_MPS-II": 1,
    "IDS-related_disorder|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases": 2,
    "Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|IDS-related_disorder|not_provided": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II": 1,
    "IDS-related_disorder|not_provided|Mucopolysaccharidosis|_MPS-III-A": 1,
    "not_provided|not_specified|Mucopolysaccharidosis|_MPS-II": 1,
    "IDS-related_disorder|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Mucopolysaccharidosis|_MPS-II": 1,
    "Mucopolysaccharidosis|_MPS-II|not_specified": 5,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A|not_provided|Mucopolysaccharidosis|_MPS-II": 1,
    "Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases|not_provided|IDS-related_disorder|Mucopolysaccharidosis|_MPS-II": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases": 1,
    "Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A|not_specified|not_provided": 1,
    "not_specified|not_provided|Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|not_specified": 1,
    "IDS-related_disorder|not_specified|Mucopolysaccharidosis|_MPS-II": 1,
    "Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-II|not_provided": 1,
    "not_provided|Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases": 1,
    "not_specified|Mucopolysaccharidosis|_MPS-II|Inborn_genetic_diseases|IDS-related_disorder": 1,
    "IDS-related_disorder|Mucopolysaccharidosis|_MPS-II|not_specified|Inborn_genetic_diseases": 1,
    "IDS-related_disorder|not_provided|Mucopolysaccharidosis|_MPS-II|Mucopolysaccharidosis|_MPS-III-A": 1,
    "Inborn_genetic_diseases|Mucopolysaccharidosis|_MPS-III-A|Mucopolysaccharidosis|_MPS-II": 1,
    "MAGEA11-related_disorder": 3,
    "MAMLD1-related_disorder": 7,
    "Hypospadias_2|_X-linked": 7,
    "Hypospadias_2|_X-linked|not_provided": 2,
    "not_provided|MAMLD1-related_disorder": 3,
    "not_provided|Hypospadias_2|_X-linked": 3,
    "not_provided|MAMLD1-related_disorder|not_specified|Hypospadias_2|_X-linked": 1,
    "not_provided|Hypospadias_2|_X-linked|MAMLD1-related_disorder": 1,
    "MAMLD1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Hypospadias_2|_X-linked|not_provided": 1,
    "MAMLD1-related_disorder|not_provided": 1,
    "46|XY_ovotesticular_disorder_of_sex_development|Hypospadias_2|_X-linked": 1,
    "Severe_X-linked_myotubular_myopathy": 568,
    "Severe_X-linked_myotubular_myopathy|Inborn_genetic_diseases": 10,
    "Inborn_genetic_diseases|not_provided|Severe_X-linked_myotubular_myopathy": 2,
    "Severe_X-linked_myotubular_myopathy|See_cases": 1,
    "Severe_X-linked_myotubular_myopathy|not_specified": 7,
    "Severe_X-linked_myotubular_myopathy|not_specified|not_provided": 1,
    "Severe_X-linked_myotubular_myopathy|not_provided": 18,
    "Inborn_genetic_diseases|Severe_X-linked_myotubular_myopathy": 7,
    "not_specified|not_provided|Severe_X-linked_myotubular_myopathy": 1,
    "not_specified|Severe_X-linked_myotubular_myopathy": 3,
    "Centronuclear_myopathy|Severe_X-linked_myotubular_myopathy": 3,
    "MTM1-related_disorder|not_provided|Centronuclear_myopathy|Severe_X-linked_myotubular_myopathy": 2,
    "MTM1-related_disorder": 5,
    "Severe_X-linked_myotubular_myopathy|not_provided|Inborn_genetic_diseases": 1,
    "Centronuclear_myopathy|not_provided|Severe_X-linked_myotubular_myopathy": 2,
    "Centronuclear_myopathy|MTM1-related_disorder|not_specified|Severe_X-linked_myotubular_myopathy|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Severe_X-linked_myotubular_myopathy": 1,
    "not_provided|Severe_X-linked_myotubular_myopathy|not_specified": 1,
    "not_provided|Centronuclear_myopathy|Severe_X-linked_myotubular_myopathy": 3,
    "Severe_X-linked_myotubular_myopathy|Centronuclear_myopathy|MTM1-related_disorder|not_specified": 1,
    "Severe_X-linked_myotubular_myopathy|Familial_Mediterranean_fever|_autosomal_dominant": 1,
    "not_provided|Severe_X-linked_myotubular_myopathy|Inborn_genetic_diseases": 2,
    "not_provided|Severe_X-linked_myotubular_myopathy|Centronuclear_myopathy": 1,
    "Severe_X-linked_myotubular_myopathy|Centronuclear_myopathy|Qualitative_or_quantitative_defects_of_myotubularin|not_provided": 1,
    "Severe_X-linked_myotubular_myopathy|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Neurodevelopmental_disorder|not_provided|Centronuclear_myopathy|Severe_X-linked_myotubular_myopathy": 1,
    "Spastic_paraplegia|not_provided|Congenital_myopathy_with_fiber_type_disproportion|Centronuclear_myopathy|Inborn_genetic_diseases|Severe_X-linked_myotubular_myopathy": 1,
    "Severe_X-linked_myotubular_myopathy|Centronuclear_myopathy": 1,
    "Severe_X-linked_myotubular_myopathy|Inborn_genetic_diseases|not_provided": 2,
    "not_specified|Severe_X-linked_myotubular_myopathy|Centronuclear_myopathy": 1,
    "Autosomal_dominant_centronuclear_myopathy|Severe_X-linked_myotubular_myopathy": 1,
    "not_specified|Centronuclear_myopathy|Severe_X-linked_myotubular_myopathy": 1,
    "Inborn_genetic_diseases|MTM1-related_disorder|Severe_X-linked_myotubular_myopathy": 1,
    "Inclusion_body_myositis": 1,
    "X-linked_colobomatous_microphthalmia-microcephaly-intellectual_disability-short_stature_syndrome": 1,
    "X-linked_colobomatous_microphthalmia-microcephaly-intellectual_disability-short_stature_syndrome|not_provided": 1,
    "HMGB3-related_disorder": 4,
    "X-linked_myopathy_with_excessive_autophagy|not_provided": 1,
    "X-linked_myopathy_with_excessive_autophagy|VMA21-related_disorder": 4,
    "VMA21-related_disorder": 2,
    "X-linked_myopathy_with_excessive_autophagy": 64,
    "X-linked_myopathy_with_excessive_autophagy|Inborn_genetic_diseases": 5,
    "Inborn_genetic_diseases|not_provided|X-linked_myopathy_with_excessive_autophagy|not_specified|VMA21-related_disorder": 1,
    "Inborn_genetic_diseases|X-linked_myopathy_with_excessive_autophagy": 2,
    "not_specified|X-linked_myopathy_with_excessive_autophagy": 1,
    "X-linked_myopathy_with_excessive_autophagy|not_specified": 1,
    "VMA21-related_disorder|X-linked_myopathy_with_excessive_autophagy": 1,
    "Inborn_genetic_diseases|X-linked_myopathy_with_excessive_autophagy|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|X-linked_myopathy_with_excessive_autophagy": 1,
    "GABRE-related_disorder": 3,
    "GABRE-related_epilepsy": 1,
    "Epilepsy|_X-linked_2|_with_or_without_impaired_intellectual_development_and_dysmorphic_features|Inborn_genetic_diseases": 1,
    "Epilepsy|_X-linked_2|_with_or_without_impaired_intellectual_development_and_dysmorphic_features": 9,
    "GABRA3-related_disorder|not_provided": 3,
    "not_provided|Epilepsy|_X-linked_2|_with_or_without_impaired_intellectual_development_and_dysmorphic_features": 1,
    "GABRA3-related_disorder": 5,
    "not_provided|GABRA3-related_disorder": 1,
    "GABRQ-related_disorder": 1,
    "NSDHL-related_disorder": 2,
    "CK_syndrome|Child_syndrome|Inborn_genetic_diseases": 1,
    "not_provided|Child_syndrome|CK_syndrome": 7,
    "not_provided|CK_syndrome": 1,
    "CK_syndrome|Child_syndrome": 8,
    "Inborn_genetic_diseases|not_provided|NSDHL-related_disorder": 1,
    "NSDHL-related_disorder|not_provided": 2,
    "CK_syndrome|Child_syndrome|not_specified|not_provided": 2,
    "Child_syndrome": 13,
    "not_provided|NSDHL-related_disorder": 3,
    "not_provided|Child_syndrome|CK_syndrome|Connective_tissue_disorder": 1,
    "not_provided|Child_syndrome": 2,
    "CK_syndrome|Child_syndrome|not_provided": 3,
    "Child_syndrome|CK_syndrome": 1,
    "CK_syndrome": 4,
    "CK_syndrome|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|CK_syndrome|Child_syndrome|not_specified": 1,
    "Child_syndrome|CK_syndrome|not_provided|not_specified": 1,
    "NSDHL-related_disorder|Inborn_genetic_diseases|not_provided": 2,
    "Child_syndrome|not_provided": 2,
    "not_provided|CK_syndrome|Child_syndrome": 1,
    "CK_syndrome|Child_syndrome|not_provided|NSDHL-related_disorder": 1,
    "not_provided|not_specified|NSDHL-related_disorder": 1,
    "Child_syndrome|CK_syndrome|not_provided": 2,
    "Unilateral_polymicrogyria|Frontoparietal_polymicrogyria|Seizure|Abnormal_cerebral_white_matter_morphology": 1,
    "not_provided|NSDHL-related_disorder|Child_syndrome|CK_syndrome": 1,
    "Inborn_genetic_diseases|Child_syndrome|CK_syndrome|not_provided": 1,
    "not_provided|CK_syndrome|Child_syndrome|NSDHL-related_disorder": 1,
    "Child_syndrome|CK_syndrome|Mitral_valve_prolapse|Joint_hypermobility|Dolichocephaly|Long_face|Tall_stature|High_palate|Scoliosis|Arachnodactyly|Delayed_speech_and_language_development|Hearing_impairment": 1,
    "CK_syndrome|Connective_tissue_disorder|Child_syndrome|not_specified|not_provided": 1,
    "Intellectual_disability|not_provided|NSDHL-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|NSDHL-related_disorder": 1,
    "Inborn_genetic_diseases|CK_syndrome|Child_syndrome": 1,
    "CK_syndrome|Child_syndrome|NSDHL-related_disorder": 1,
    "NSDHL-related_disorder|Child_syndrome": 1,
    "not_specified|ZFP92-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Meester-Loeys_syndrome": 2,
    "X-linked_spondyloepimetaphyseal_dysplasia|Cardiovascular_phenotype|not_provided": 1,
    "BGN-related_disorder": 3,
    "Meester-Loeys_syndrome": 8,
    "Meester-Loeys_syndrome|not_provided": 2,
    "Meester-Loeys_syndrome|Familial_aortopathy": 1,
    "BGN-related_disorder|not_provided": 2,
    "not_specified|Cardiovascular_phenotype|X-linked_spondyloepimetaphyseal_dysplasia|Meester-Loeys_syndrome|not_provided": 1,
    "not_provided|BGN-related_disorder|Cardiovascular_phenotype|not_specified": 1,
    "BGN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "Meester-Loeys_syndrome|Cardiovascular_phenotype|not_provided|X-linked_spondyloepimetaphyseal_dysplasia|not_specified": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia|Meester-Loeys_syndrome": 3,
    "Meester-Loeys_syndrome|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "not_provided|Meester-Loeys_syndrome": 3,
    "X-linked_spondyloepimetaphyseal_dysplasia|Meester-Loeys_syndrome|Cardiovascular_phenotype|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia|Meester-Loeys_syndrome|not_provided": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia|Meester-Loeys_syndrome|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|BGN-related_disorder|not_provided": 1,
    "not_provided|BGN-related_disorder": 3,
    "not_provided|not_specified|BGN-related_disorder|Cardiovascular_phenotype": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia": 4,
    "Meester-Loeys_syndrome|Cardiovascular_phenotype|X-linked_spondyloepimetaphyseal_dysplasia|not_specified|not_provided": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia|Meester-Loeys_syndrome|Cardiovascular_phenotype": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia|not_provided|Meester-Loeys_syndrome": 2,
    "not_provided|X-linked_spondyloepimetaphyseal_dysplasia": 1,
    "not_specified|BGN-related_disorder|Cardiovascular_phenotype|not_provided": 1,
    "BGN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Cardiovascular_phenotype|not_provided|Meester-Loeys_syndrome|X-linked_spondyloepimetaphyseal_dysplasia": 1,
    "ATP2B3-related_disorder": 12,
    "X-linked_progressive_cerebellar_ataxia": 14,
    "ATP2B3-related_disorder|not_provided": 4,
    "not_provided|X-linked_progressive_cerebellar_ataxia": 7,
    "Inborn_genetic_diseases|X-linked_progressive_cerebellar_ataxia": 2,
    "not_provided|ATP2B3-related_disorder": 2,
    "not_specified|not_provided|X-linked_progressive_cerebellar_ataxia": 3,
    "ATP2B3-related_disorder|Inborn_genetic_diseases": 1,
    "X-linked_progressive_cerebellar_ataxia|not_specified|not_provided": 2,
    "Inborn_genetic_diseases|ATP2B3-related_disorder": 1,
    "not_specified|X-linked_progressive_cerebellar_ataxia": 1,
    "Neonatal_hypotonia": 1,
    "not_provided|not_specified|X-linked_progressive_cerebellar_ataxia": 1,
    "X-linked_progressive_cerebellar_ataxia|not_provided": 2,
    "Inborn_genetic_diseases|not_provided|X-linked_progressive_cerebellar_ataxia": 1,
    "Microcephaly|Intellectual_disability|Muscular_atrophy|Global_developmental_delay|Oral-pharyngeal_dysphagia|Abnormal_cerebral_cortex_morphology|Carious_teeth|Hypotonia|X-linked_progressive_cerebellar_ataxia": 1,
    "Syndactyly-telecanthus-anogenital_and_renal_malformations_syndrome": 6,
    "CCNQ-related_disorder": 5,
    "PNCK-related_condition": 1,
    "SLC6A8-related_disorder|Creatine_transporter_deficiency|not_specified|Inborn_genetic_diseases|not_provided|Creatine_deficiency_syndrome_1": 1,
    "Creatine_deficiency_syndrome_1": 20,
    "Creatine_transporter_deficiency": 723,
    "not_provided|Creatine_transporter_deficiency": 47,
    "Creatine_transporter_deficiency|not_provided": 52,
    "Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency": 13,
    "Creatine_transporter_deficiency|Creatine_deficiency_syndrome_1": 9,
    "not_specified|Creatine_transporter_deficiency": 24,
    "Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency|Inborn_genetic_diseases": 1,
    "Creatine_transporter_deficiency|Creatine_deficiency_syndrome_1|not_provided": 3,
    "Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency|SLC6A8-related_disorder": 1,
    "not_provided|not_specified|Creatine_transporter_deficiency|Creatine_deficiency_syndrome_1": 1,
    "not_specified|not_provided|Creatine_transporter_deficiency": 1,
    "not_provided|Inborn_genetic_diseases|Creatine_transporter_deficiency": 1,
    "Creatine_deficiency_syndrome_1|Inborn_genetic_diseases|Creatine_transporter_deficiency": 2,
    "SLC6A8-related_disorder|Creatine_transporter_deficiency|not_specified": 1,
    "Creatine_transporter_deficiency|Inborn_genetic_diseases": 13,
    "Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency|not_provided": 3,
    "not_specified|not_provided|Creatine_transporter_deficiency|SLC6A8-related_disorder": 1,
    "Creatine_transporter_deficiency|not_provided|Inborn_genetic_diseases": 4,
    "Creatine_transporter_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Inborn_genetic_diseases|SLC6A8-related_disorder": 1,
    "Creatine_transporter_deficiency|SLC6A8-related_disorder|not_provided": 3,
    "Creatine_transporter_deficiency|not_specified": 21,
    "Creatine_transporter_deficiency|Inborn_genetic_diseases|Creatine_deficiency_syndrome_1|not_provided": 1,
    "not_specified|Inborn_genetic_diseases|Creatine_transporter_deficiency|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Creatine_transporter_deficiency": 4,
    "not_provided|Creatine_transporter_deficiency|not_specified|Inborn_genetic_diseases": 2,
    "Creatine_transporter_deficiency|not_specified|SLC6A8-related_disorder": 1,
    "not_provided|Creatine_transporter_deficiency|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|Creatine_transporter_deficiency|SLC6A8-related_disorder|not_provided": 1,
    "Creatine_transporter_deficiency|SLC6A8-related_disorder": 3,
    "not_provided|Creatine_transporter_deficiency|SLC6A8-related_disorder": 1,
    "SLC6A8-related_disorder|Inborn_genetic_diseases|not_specified|Creatine_transporter_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|Creatine_transporter_deficiency": 2,
    "not_specified|SLC6A8-related_disorder|not_provided|Creatine_transporter_deficiency|Inborn_genetic_diseases|Rhombencephalosynapsis": 1,
    "SLC6A8-related_disorder|Creatine_transporter_deficiency|not_provided": 1,
    "Creatine_transporter_deficiency|not_provided|SLC6A8-related_disorder|not_specified": 1,
    "not_specified|Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency": 1,
    "not_provided|Creatine_deficiency_syndrome_1": 2,
    "not_specified|Creatine_transporter_deficiency|not_provided": 1,
    "SLC6A8-related_disorder": 4,
    "Creatine_transporter_deficiency|Intellectual_disability": 1,
    "Creatine_transporter_deficiency|SLC6A8-related_disorder|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Creatine_transporter_deficiency": 2,
    "not_provided|Creatine_transporter_deficiency|Inborn_genetic_diseases|not_specified": 1,
    "not_provided|not_specified|Creatine_transporter_deficiency": 1,
    "Creatine_transporter_deficiency|Intellectual_disability|not_provided": 1,
    "not_provided|Creatine_deficiency_syndrome_1|Inborn_genetic_diseases|not_specified|Creatine_transporter_deficiency": 2,
    "Creatine_transporter_deficiency|Creatine_deficiency_syndrome_1|not_specified": 1,
    "Inborn_genetic_diseases|Creatine_transporter_deficiency|not_provided": 2,
    "Creatine_transporter_deficiency|not_provided|Creatine_deficiency_syndrome_1": 3,
    "Abnormal_facial_shape|Low-set_ears|Seizure|Intellectual_disability": 1,
    "Creatine_deficiency_syndrome_1|SLC6A8-related_disorder|Creatine_transporter_deficiency": 1,
    "not_provided|SLC6A8-related_disorder|Creatine_transporter_deficiency": 1,
    "Creatine_deficiency_syndrome_1|not_provided|Creatine_transporter_deficiency|Inborn_genetic_diseases": 2,
    "not_specified|Inborn_genetic_diseases|Creatine_transporter_deficiency": 1,
    "Inborn_genetic_diseases|Creatine_transporter_deficiency": 2,
    "Creatine_deficiency_syndrome_1|Inborn_genetic_diseases|not_provided|Creatine_transporter_deficiency": 1,
    "not_specified|Creatine_transporter_deficiency|See_cases|not_provided": 1,
    "not_provided|Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency": 2,
    "not_provided|Creatine_transporter_deficiency|not_specified|SLC6A8-related_disorder": 1,
    "SLC6A8-related_disorder|Creatine_transporter_deficiency": 4,
    "SLC6A8-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Creatine_transporter_deficiency|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|Creatine_transporter_deficiency|not_provided|Creatine_deficiency_syndrome_1": 1,
    "SLC6A8-related_disorder|Creatine_transporter_deficiency|Creatine_deficiency_syndrome_1": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Creatine_transporter_deficiency": 1,
    "not_provided|Creatine_transporter_deficiency|SLC6A8-related_disorder|not_specified": 1,
    "Creatine_deficiency_syndrome_1|not_provided|Creatine_transporter_deficiency": 1,
    "not_specified|Creatine_transporter_deficiency|not_provided|Creatine_deficiency_syndrome_1|Inborn_genetic_diseases": 1,
    "Creatine_transporter_deficiency|not_specified|not_provided": 1,
    "not_provided|Creatine_transporter_deficiency|Inborn_genetic_diseases|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|Creatine_transporter_deficiency|Inborn_genetic_diseases": 1,
    "SLC6A8-related_disorder|not_provided|Inborn_genetic_diseases|Creatine_transporter_deficiency": 1,
    "not_provided|Creatine_transporter_deficiency|not_specified": 2,
    "Creatine_deficiency_syndrome_1|not_specified|Creatine_transporter_deficiency|Inborn_genetic_diseases": 1,
    "SLC6A8-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Creatine_transporter_deficiency": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Congenital_cerebellar_hypoplasia|Creatine_transporter_deficiency": 1,
    "Creatine_transporter_deficiency|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "not_specified|Creatine_deficiency_syndrome_1|Inborn_genetic_diseases|not_provided|SLC6A8-related_disorder|Creatine_transporter_deficiency": 1,
    "Inborn_genetic_diseases|not_provided|Creatine_transporter_deficiency|SLC6A8-related_disorder": 1,
    "not_specified|Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency|Inborn_genetic_diseases": 2,
    "not_provided|Creatine_transporter_deficiency|Creatine_deficiency_syndrome_1": 2,
    "Creatine_deficiency_syndrome_1|Creatine_transporter_deficiency|Inborn_genetic_diseases|not_provided": 1,
    "Severe_motor_and_intellectual_disabilities-sensorineural_deafness-dystonia_syndrome": 10,
    "BCAP31-related_disorder": 5,
    "Severe_motor_and_intellectual_disabilities-sensorineural_deafness-dystonia_syndrome|not_provided": 2,
    "not_provided|BCAP31-related_disorder": 5,
    "Severe_motor_and_intellectual_disabilities-sensorineural_deafness-dystonia_syndrome|Inborn_genetic_diseases": 1,
    "Global_developmental_delay|Seizure|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|BCAP31-related_disorder": 2,
    "Adrenoleukodystrophy": 1044,
    "Adrenoleukodystrophy|not_provided": 87,
    "not_specified|Adrenoleukodystrophy": 10,
    "not_provided|Adrenoleukodystrophy|Inborn_genetic_diseases": 5,
    "not_provided|Adrenoleukodystrophy": 114,
    "Adrenoleukodystrophy|not_specified": 12,
    "Adrenoleukodystrophy|Inborn_genetic_diseases|not_provided|not_specified": 3,
    "not_specified|not_provided|Adrenoleukodystrophy|Inborn_genetic_diseases": 2,
    "not_provided|Inborn_genetic_diseases|ABCD1-related_disorder|Adrenoleukodystrophy": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Adrenoleukodystrophy": 1,
    "Inborn_genetic_diseases|not_provided|ABCD1-related_disorder|Adrenoleukodystrophy": 1,
    "ABCD1-related_disorder|Adrenoleukodystrophy": 6,
    "Inborn_genetic_diseases|Adrenoleukodystrophy": 12,
    "X-linked_cerebral_adrenoleukodystrophy": 1,
    "Adrenoleukodystrophy|Inborn_genetic_diseases|not_specified": 1,
    "ABCD1-related_disorder": 14,
    "Adrenoleukodystrophy|Inborn_genetic_diseases": 17,
    "Inborn_genetic_diseases|not_specified|not_provided|Adrenoleukodystrophy": 1,
    "not_provided|Inborn_genetic_diseases|Adrenoleukodystrophy": 9,
    "Adrenoleukodystrophy|ABCD1-related_disorder": 5,
    "ABCD1-related_disorder|Inborn_genetic_diseases|not_provided|Adrenoleukodystrophy": 2,
    "Inborn_genetic_diseases|Adrenoleukodystrophy|not_provided": 4,
    "Inborn_genetic_diseases|not_provided|Adrenoleukodystrophy": 11,
    "Adrenoleukodystrophy|Inborn_genetic_diseases|not_provided|ABCD1-related_disorder": 1,
    "Adrenoleukodystrophy|ABCD1-related_disorder|not_provided": 6,
    "Adrenoleukodystrophy|not_provided|ABCD1-related_disorder": 2,
    "not_specified|ABCD1-related_disorder|Adrenoleukodystrophy|not_provided": 1,
    "ABCD1-related_disorder|Adrenoleukodystrophy|not_provided": 2,
    "ABCD1-related_disorder|not_provided": 6,
    "Adrenoleukodystrophy|not_provided|Inborn_genetic_diseases": 2,
    "Inborn_genetic_diseases|Adrenoleukodystrophy|ABCD1-related_disorder": 1,
    "Adrenoleukodystrophy|not_provided|not_specified": 1,
    "not_specified|Adrenoleukodystrophy|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Adrenoleukodystrophy|ABCD1-related_disorder|not_provided": 2,
    "Adrenoleukodystrophy|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|X-linked_spondyloepimetaphyseal_dysplasia|Adrenoleukodystrophy|not_provided": 1,
    "not_provided|not_specified|ABCD1-related_disorder|Adrenoleukodystrophy": 1,
    "Inborn_genetic_diseases|Adrenoleukodystrophy|not_specified": 1,
    "Adrenoleukodystrophy|not_provided|not_specified|ABCD1-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Adrenoleukodystrophy|ABCD1-related_disorder": 2,
    "ABCD1-related_disorder|History_of_neurodevelopmental_disorder|not_provided|Adrenoleukodystrophy": 1,
    "not_provided|Adrenoleukodystrophy|not_specified": 2,
    "not_specified|Inborn_genetic_diseases|Adrenoleukodystrophy|not_provided": 1,
    "not_specified|Intellectual_disability|Adrenoleukodystrophy": 1,
    "ABCD1-related_disorder|not_provided|Adrenoleukodystrophy": 10,
    "not_provided|ABCD1-related_disorder": 1,
    "not_specified|Adrenoleukodystrophy|not_provided": 2,
    "not_specified|not_provided|Adrenoleukodystrophy": 9,
    "Inborn_genetic_diseases|not_provided|not_specified|Adrenoleukodystrophy|ABCD1-related_disorder": 1,
    "not_provided|Intellectual_disability|Adrenoleukodystrophy": 1,
    "Adrenoleukodystrophy|not_specified|Inborn_genetic_diseases": 1,
    "not_provided|not_specified|Adrenoleukodystrophy": 3,
    "Adrenoleukodystrophy|Inborn_genetic_diseases|not_provided": 2,
    "not_provided|not_specified|Adrenoleukodystrophy|Inborn_genetic_diseases": 1,
    "X-linked_spondyloepimetaphyseal_dysplasia|not_provided|Adrenoleukodystrophy": 1,
    "not_provided|ABCD1-related_disorder|Adrenoleukodystrophy|Inborn_genetic_diseases": 1,
    "ABCD1-related_disorder|Adrenoleukodystrophy|not_provided|Inborn_genetic_diseases": 1,
    "Adrenoleukodystrophy|not_provided|EBV-positive_nodal_T-_and_NK-cell_lymphoma": 1,
    "Adrenoleukodystrophy|Inborn_genetic_diseases|ABCD1-related_disorder|not_specified|not_provided": 1,
    "Adrenoleukodystrophy|ABCD1-related_disorder|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|not_specified|ABCD1-related_disorder|Adrenoleukodystrophy": 1,
    "Adrenoleukodystrophy|not_provided|not_specified|ABCD1-related_disorder": 1,
    "not_provided|Inborn_genetic_diseases|Ehlers-Danlos_syndrome|_kyphoscoliotic_type_1|Adrenoleukodystrophy": 1,
    "X-linked_cerebral_adrenoleukodystrophy|not_specified|Adrenoleukodystrophy": 1,
    "Primary_adrenocortical_insufficiency|not_provided|Adrenoleukodystrophy": 1,
    "Primary_adrenocortical_insufficiency": 1,
    "not_provided|Adrenoleukodystrophy|ABCD1-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Adrenoleukodystrophy|Spastic_paraplegia|Spastic_gait": 1,
    "Adrenoleukodystrophy|Encephalitis|Episodic_vomiting|Myocarditis|Recurrent_fever": 1,
    "not_provided|ABCD1-related_disorder|Adrenoleukodystrophy": 2,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Adrenoleukodystrophy": 1,
    "PLXNB3-related_Intellectual_disability": 1,
    "PLXNB3-related_disorder": 9,
    "not_specified|PLXNB3-related_disorder": 2,
    "Intellectual_developmental_disorder|_X-linked_114": 2,
    "SRPK3-related_disorder": 1,
    "RETINITIS_PIGMENTOSA_99": 2,
    "not_provided|SSR4-related_disorder": 1,
    "SSR4-related_disorder": 4,
    "SSR4-congenital_disorder_of_glycosylation": 17,
    "Autism|Hypotonia|Hand_tremor|Abnormal_facial_shape|Kyphoscoliosis": 1,
    "Microcephaly|Intellectual_disability|Coarse_facial_features|Hyperactivity|Movement_disorder": 1,
    "L1CAM-related_disorder|Spastic_paraplegia": 5,
    "Spastic_paraplegia|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome": 2,
    "MASA_syndrome": 12,
    "X-linked_complicated_corpus_callosum_dysgenesis": 5,
    "not_provided|L1CAM-related_disorder|L1_syndrome": 1,
    "Inborn_genetic_diseases|MASA_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|L1CAM-related_disorder|not_specified|Spastic_paraplegia": 1,
    "L1_syndrome": 11,
    "Spastic_paraplegia|X-linked_hydrocephalus_syndrome|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis": 1,
    "Hydrops_fetalis|Severe_hydrocephalus|not_provided|X-linked_hydrocephalus_syndrome|MASA_syndrome|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|MASA_syndrome": 1,
    "Spastic_paraplegia|MASA_syndrome|not_provided": 1,
    "MASA_syndrome|not_provided": 1,
    "L1CAM-related_disorder": 19,
    "L1CAM-related_disorders": 1,
    "L1CAM-related_disorder|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "not_provided|not_specified|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|See_cases": 1,
    "X-linked_complicated_corpus_callosum_dysgenesis|MASA_syndrome|X-linked_hydrocephalus_syndrome": 2,
    "X-linked_hydrocephalus_syndrome|MASA_syndrome": 3,
    "L1CAM-related_disorder|not_provided|Spastic_paraplegia": 1,
    "L1_syndrome|not_provided": 1,
    "Spastic_paraplegia|X-linked_complicated_corpus_callosum_dysgenesis": 1,
    "not_provided|Spastic_paraplegia|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome": 1,
    "not_specified|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|L1CAM-related_disorder": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified|not_provided": 2,
    "Spastic_paraplegia|Hydrocephalus_due_to_aqueductal_stenosis": 2,
    "X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome|MASA_syndrome": 2,
    "Spastic_paraplegia|L1CAM-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Hydrocephalus|_X-linked|_with_congenital_idiopathic_intestinal_pseudoobstruction": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|not_provided": 1,
    "not_specified|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "X-linked_complicated_corpus_callosum_dysgenesis|MASA_syndrome|X-linked_hydrocephalus_syndrome|not_specified|Spastic_paraplegia": 1,
    "MASA_syndrome|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|Aganglionic_megacolon": 1,
    "MASA_syndrome|X-linked_hydrocephalus_syndrome|X-linked_complicated_corpus_callosum_dysgenesis": 2,
    "L1CAM-related_disorder|not_provided": 1,
    "Hereditary_spastic_paraplegia|Hydrocephalus_due_to_aqueductal_stenosis|not_specified|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "not_provided|X-linked_complicated_corpus_callosum_dysgenesis|MASA_syndrome|X-linked_hydrocephalus_syndrome": 2,
    "MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome|Spastic_paraplegia": 1,
    "X-linked_hydrocephalus_syndrome|L1_syndrome": 1,
    "Hydrocephalus_due_to_aqueductal_stenosis": 1,
    "Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|Inborn_genetic_diseases|not_specified": 2,
    "Inborn_genetic_diseases|Spastic_paraplegia|Hereditary_ataxia|not_specified|not_provided|Hereditary_spastic_paraplegia": 1,
    "Hydrocephalus_due_to_aqueductal_stenosis|L1_syndrome|not_provided|X-linked_hydrocephalus_syndrome|X-linked_complicated_corpus_callosum_dysgenesis": 1,
    "Spastic_paraplegia|X-linked_hydrocephalus_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_specified|Hereditary_spastic_paraplegia|not_provided|Inborn_genetic_diseases": 1,
    "Spastic_paraplegia|L1CAM-related_disorder": 8,
    "Inborn_genetic_diseases|not_specified|not_provided|Spastic_paraplegia": 2,
    "L1CAM-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|not_provided|not_specified|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|X-linked_hydrocephalus_syndrome": 2,
    "X-linked_hydrocephalus_syndrome|not_provided": 2,
    "Hereditary_spastic_paraplegia|not_specified|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "L1CAM-related_disorders|not_provided|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|not_provided|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "Spastic_paraplegia|MASA_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "not_specified|Spastic_paraplegia|Hereditary_spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_specified|Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia": 1,
    "L1CAM-related_disorder|Spastic_paraplegia|not_provided": 4,
    "X-linked_hydrocephalus_syndrome|not_provided|Spastic_paraplegia": 1,
    "Spastic_paraplegia|X-linked_hydrocephalus_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|MASA_syndrome|not_provided": 1,
    "L1_syndrome|not_provided|MASA_syndrome|Spastic_paraplegia": 1,
    "not_provided|L1_syndrome|Spastic_paraplegia|Hydrocephalus_due_to_aqueductal_stenosis|X-linked_hydrocephalus_syndrome": 1,
    "L1CAM-related_disorder|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "Hereditary_spastic_paraplegia|not_provided|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "MASA_syndrome|Spastic_paraplegia": 2,
    "Spastic_paraplegia|not_provided|not_specified|Inborn_genetic_diseases|Hereditary_spastic_paraplegia": 1,
    "Spastic_paraplegia|not_provided|L1_syndrome": 1,
    "not_provided|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "not_provided|Spastic_paraplegia|Inborn_genetic_diseases|X-linked_hydrocephalus_syndrome|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis": 1,
    "Spastic_paraplegia|MASA_syndrome|X-linked_hydrocephalus_syndrome|L1CAM-related_disorders|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|not_specified|Spastic_paraplegia": 1,
    "MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|not_provided|L1_syndrome|X-linked_hydrocephalus_syndrome|X-linked_complicated_corpus_callosum_dysgenesis": 1,
    "not_provided|X-linked_hydrocephalus_syndrome|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "not_specified|X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome|MASA_syndrome": 1,
    "Cerebellar_ataxia|Peripheral_neuropathy": 1,
    "Spastic_paraplegia|L1CAM-related_disorder|Inborn_genetic_diseases|MASA_syndrome|X-linked_hydrocephalus_syndrome|X-linked_complicated_corpus_callosum_dysgenesis": 1,
    "X-linked_hydrocephalus_syndrome|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|L1_syndrome|not_provided|Spastic_paraplegia": 1,
    "Hereditary_spastic_paraplegia|not_specified|not_provided|Inborn_genetic_diseases|Spastic_paraplegia": 1,
    "L1CAM-related_disorder|Spastic_paraplegia|L1_syndrome|X-linked_hydrocephalus_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|MASA_syndrome|not_provided|Congenital_cerebellar_hypoplasia": 1,
    "not_provided|X-linked_hydrocephalus_syndrome": 1,
    "Spastic_paraplegia|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|Inborn_genetic_diseases|X-linked_hydrocephalus_syndrome|not_provided": 1,
    "not_provided|X-linked_hydrocephalus_syndrome|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|L1CAM-related_disorder|Spastic_paraplegia": 1,
    "Inborn_genetic_diseases|Spastic_paraplegia|L1_syndrome|X-linked_hydrocephalus_syndrome": 1,
    "L1_syndrome|Spastic_paraplegia|not_provided": 1,
    "Inborn_genetic_diseases|not_provided|Spastic_paraplegia|MASA_syndrome|X-linked_complicated_corpus_callosum_dysgenesis|X-linked_hydrocephalus_syndrome": 1,
    "not_provided|Spastic_paraplegia|L1CAM-related_disorder": 1,
    "Spastic_paraplegia|L1CAM-related_disorder|History_of_neurodevelopmental_disorder": 1,
    "not_specified|not_provided|Spastic_paraplegia|Inborn_genetic_diseases": 1,
    "L1CAM-related_disorder|not_specified": 1,
    "not_provided|X-linked_complicated_corpus_callosum_dysgenesis|MASA_syndrome|X-linked_hydrocephalus_syndrome|L1CAM-related_disorder|Inborn_genetic_diseases|Spastic_paraplegia|not_specified": 1,
    "Hereditary_spastic_paraplegia|Inborn_genetic_diseases|Spastic_paraplegia|not_specified": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked": 47,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis|not_specified|not_provided": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|AVPR2-related_disorder|not_provided": 1,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|not_specified|not_provided": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis": 24,
    "Diabetes_insipidus|_nephrogenic|_X-linked|not_provided|not_specified": 1,
    "AVPR2-related_disorder": 9,
    "not_provided|Diabetes_insipidus|_nephrogenic|_X-linked": 7,
    "Inborn_genetic_diseases|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked": 2,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis|not_provided|AVPR2-related_disorder": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis|not_provided|not_specified": 2,
    "Diabetes_insipidus|_nephrogenic|_X-linked|not_provided": 15,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked": 1,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis": 2,
    "not_provided|Diabetes_insipidus|_nephrogenic|_X-linked|not_specified|Nephrogenic_syndrome_of_inappropriate_antidiuresis": 1,
    "not_provided|Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis": 6,
    "not_provided|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked": 2,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|not_provided|Nephrogenic_diabetes_insipidus": 1,
    "not_provided|AVPR2-related_disorder": 1,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|not_provided": 4,
    "not_provided|Diabetes_insipidus|_nephrogenic|_X-linked|Inborn_genetic_diseases": 1,
    "not_provided|Nephrogenic_syndrome_of_inappropriate_antidiuresis": 1,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_diabetes_insipidus|not_provided": 1,
    "not_specified|Nephrogenic_diabetes_insipidus": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|not_specified|not_provided": 2,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis|not_provided": 3,
    "Inborn_genetic_diseases|AVPR2-related_disorder": 1,
    "not_specified|Diabetes_insipidus|_nephrogenic|_X-linked": 1,
    "AVPR2-related_disorder|not_provided": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_diabetes_insipidus": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Inborn_genetic_diseases|not_provided": 1,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|Inborn_genetic_diseases": 1,
    "not_provided|Diabetes_insipidus|_nephrogenic|_X-linked|AVPR2-related_disorder": 1,
    "not_provided|not_specified|Diabetes_insipidus|_nephrogenic|_X-linked": 1,
    "Nephrogenic_diabetes_insipidus|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|AVPR2-related_disorder": 1,
    "AVPR2-related_disorder|Diabetes_insipidus|_nephrogenic|_X-linked|Nephrogenic_syndrome_of_inappropriate_antidiuresis": 1,
    "Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|not_provided|not_specified": 1,
    "Diabetes_insipidus|_nephrogenic|_X-linked|not_provided|Nephrogenic_syndrome_of_inappropriate_antidiuresis": 1,
    "not_provided|Diabetes_insipidus|_nephrogenic|_X-linked|not_specified": 1,
    "Inborn_genetic_diseases|Nephrogenic_syndrome_of_inappropriate_antidiuresis|Diabetes_insipidus|_nephrogenic|_X-linked|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|not_specified|Diabetes_insipidus|_nephrogenic|_X-linked": 1,
    "Xq28_related_immunodeficiency": 1,
    "Microphthalmia|_syndromic_1": 2,
    "not_provided|Microphthalmia|_syndromic_1": 3,
    "not_provided|NAA10-related_disorder": 4,
    "not_provided|Ogden_syndrome|Microphthalmia|_syndromic_1": 1,
    "Ogden_syndrome": 20,
    "NAA10-related_disorder": 3,
    "not_provided|Inborn_genetic_diseases|Ogden_syndrome": 1,
    "Inborn_genetic_diseases|Microphthalmia|_syndromic_1|Ogden_syndrome|not_provided": 1,
    "Microphthalmia|_syndromic_1|Ogden_syndrome": 3,
    "not_provided|Ogden_syndrome": 6,
    "Intellectual_disability|Ogden_syndrome": 1,
    "not_provided|NAA10-related_disorder|Ogden_syndrome": 1,
    "NAA10-related_disorder|not_provided|Ogden_syndrome": 1,
    "NAA10-related_disorder|Intellectual_disability": 1,
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    "Inborn_genetic_diseases|Ogden_syndrome": 1,
    "NAA10-related_disorder|Inborn_genetic_diseases|not_provided|Ogden_syndrome|Intellectual_disability|See_cases": 1,
    "not_provided|Ogden_syndrome|not_specified|Intellectual_disability": 1,
    "Microphthalmia|_syndromic_1|Ogden_syndrome|not_provided": 1,
    "not_specified|NAA10-related_disorder|not_provided": 1,
    "Ogden_syndrome|Microphthalmia|_syndromic_1": 2,
    "Microphthalmia|_syndromic_1|Intellectual_disability|Intellectual_disability|_severe|Neurodevelopmental_disorder": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 886,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 32,
    "not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 47,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified": 33,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified|not_provided": 6,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|Inborn_genetic_diseases": 10,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided": 31,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified": 4,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder": 9,
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    "not_provided|HCFC1-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "not_provided|Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 3,
    "Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 15,
    "not_specified|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 5,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "HCFC1-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 3,
    "Inborn_genetic_diseases|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided": 2,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|Intellectual_disability": 1,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|Inborn_genetic_diseases": 4,
    "not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided": 5,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|See_cases|Inborn_genetic_diseases|not_provided": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder|not_provided|not_specified": 1,
    "Inborn_genetic_diseases|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 2,
    "not_provided|not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "HCFC1-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified|not_provided": 1,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder|not_specified": 2,
    "HCFC1-related_disorders": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided|Inborn_genetic_diseases": 2,
    "not_provided|Genetic_developmental_and_epileptic_encephalopathy|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified": 1,
    "Inborn_genetic_diseases|not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "HCFC1-related_disorder|not_specified|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 2,
    "HCFC1-related_disorder": 4,
    "Autosomal_recessive_disease|HCFC1-related_disorder|not_specified|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "HCFC1-related_disorder|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder|not_provided": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_specified|HCFC1-related_disorder|not_provided": 1,
    "not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder": 1,
    "not_specified|HCFC1-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided": 1,
    "not_specified|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX|HCFC1-related_disorder": 1,
    "not_specified|HCFC1-related_disorder|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided|not_specified": 3,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "HCFC1-related_disorder|not_specified|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "Methylmalonic_acidemia_with_homocystinuria|_type_cblX|not_provided|HCFC1-related_disorder": 1,
    "Disorders_of_Intracellular_Cobalamin_Metabolism|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 2,
    "Intellectual_disability|Cobalamin_C_disease|Disorders_of_Intracellular_Cobalamin_Metabolism|not_provided|Methylmalonic_acidemia_with_homocystinuria|_type_cblX": 1,
    "IRAK1-related_disorder|not_specified": 1,
    "not_provided|IRAK1-related_disorder": 3,
    "IRAK1-related_disorder": 11,
    "Cleft_palate|Fetal_distress|Apneic_episodes_in_infancy|Unilateral_ptosis|Inguinal_hernia|High_palate": 1,
    "IRAK1-related_disorder|not_provided": 1,
    "IRAK1-related_disorder|not_specified|not_provided": 1,
    "Rett_syndrome|not_specified": 26,
    "not_specified|Rett_syndrome": 19,
    "Rett_syndrome|not_provided|not_specified": 7,
    "not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3": 5,
    "not_specified|not_provided|Rett_syndrome": 3,
    "Autism|_susceptibility_to|_X-linked_3|Rett_syndrome": 4,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly": 453,
    "Rett_syndrome|Autism|_susceptibility_to|_X-linked_3": 7,
    "Rett_syndrome|not_specified|not_provided": 3,
    "MECP2-related_disorder": 35,
    "MECP2-related_disorder|not_specified|not_provided|Rett_syndrome": 1,
    "not_specified|Rett_syndrome|not_provided": 4,
    "MECP2-related_disorder|Rett_syndrome|not_specified|not_provided": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|not_provided|Rett_syndrome|MECP2-related_disorder|History_of_neurodevelopmental_disorder": 1,
    "not_specified|Rett_syndrome|MECP2-related_disorder": 1,
    "not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 21,
    "MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 13,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 17,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 33,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|not_specified|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_specified": 6,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|not_provided|not_specified|Inborn_genetic_diseases": 1,
    "Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|not_provided|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 3,
    "not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome": 1,
    "not_provided|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 7,
    "Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 10,
    "not_provided|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome": 2,
    "Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|not_specified|not_provided": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 29,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided|not_specified": 2,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder": 19,
    "not_provided|MECP2-related_disorder": 3,
    "not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 7,
    "MECP2-related_disorder|not_specified|not_provided|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 4,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 2,
    "Rett_syndrome|Intellectual_disability|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Rett_syndrome": 5,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 9,
    "MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 2,
    "not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly": 7,
    "MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 2,
    "not_specified|Rett_syndrome|MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|MECP2-related_disorder|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|Intellectual_disability|not_specified|Inborn_genetic_diseases": 1,
    "not_specified|Rett_syndrome|MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 26,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder": 4,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided": 10,
    "Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 2,
    "Inborn_genetic_diseases|MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Attention_deficit_hyperactivity_disorder": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Inborn_genetic_diseases|not_specified": 1,
    "MECP2-related_disorder|Developmental_and_epileptic_encephalopathy|_2|Rett_syndrome": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified": 3,
    "MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 14,
    "not_provided|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Rett_syndrome|Inborn_genetic_diseases": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|not_specified|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "See_cases|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Inborn_genetic_diseases": 2,
    "Autism|_susceptibility_to|_X-linked_3": 4,
    "Epilepsy|Intellectual_disability": 1,
    "not_specified|Inborn_genetic_diseases|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 1,
    "History_of_neurodevelopmental_disorder|not_specified|Rett_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Rett_syndrome|Encephalopathy|_neonatal_severeMental_retardation|_X-linked|_syndromic_13Rett_syndrome|not_provided": 1,
    "not_provided|Rett_syndrome|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly": 2,
    "MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Rett_syndrome|not_provided|Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_provided|Rett_syndrome|Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Atypical_Rett_syndrome|Angelman_syndrome|Rett_syndrome": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome|MECP2-related_disorder|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Rett_syndrome|not_provided": 1,
    "Inborn_genetic_diseases|Smith-Magenis_Syndrome-like|MECP2-related_disorder|not_specified|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|_zappella_variant|See_cases|Delayed_gross_motor_development|Loss_of_ambulation|Delayed_speech_and_language_development": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|Neurodevelopmental_delay|not_provided": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly": 5,
    "Rett_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 6,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 5,
    "Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Angelman_syndrome|Rett_syndrome": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_provided": 1,
    "not_provided|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|Rett_syndrome|_zappella_variant|See_cases": 1,
    "History_of_neurodevelopmental_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_specified|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|not_specified|Rett_syndrome|Inborn_genetic_diseases": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Inborn_genetic_diseases|not_provided": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 2,
    "not_provided|Inborn_genetic_diseases|Rett_syndrome": 1,
    "Attention_deficit_hyperactivity_disorder|Rett_syndrome": 1,
    "not_specified|Rett_syndrome|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_provided|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 2,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|Rett_syndrome|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases": 8,
    "not_provided|Rett_syndrome|not_specified|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_provided|Neurodevelopmental_delay|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Rett_syndrome": 1,
    "MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 2,
    "Rett_syndrome|MECP2-related_disorder": 3,
    "not_provided|Angelman_syndrome|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Rett_syndrome": 3,
    "not_provided|Rett_syndrome|Inborn_genetic_diseases": 2,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_specified|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Intellectual_disability|not_provided": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Intellectual_disability|Inborn_genetic_diseases|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|History_of_neurodevelopmental_disorder": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Intellectual_disability": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided|MECP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|MECP2-related_disorder": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|not_specified|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome": 1,
    "Developmental_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Rett_syndrome|Inborn_genetic_diseases": 2,
    "MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 3,
    "MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Rett_syndrome|Neurodevelopmental_delay|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided|Inborn_genetic_diseases": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|not_provided": 1,
    "Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Intellectual_disability|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 1,
    "MECP2-related_disorder|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Inborn_genetic_diseases|MECP2-related_disorder|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "History_of_neurodevelopmental_disorder|MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 3,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|not_provided": 2,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 3,
    "MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 2,
    "Rett_syndrome|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly": 2,
    "Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified": 7,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 6,
    "Syndromic_X-linked_intellectual_disability_Lubs_type": 3,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Inborn_genetic_diseases|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome": 6,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Seizure|Inborn_genetic_diseases": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Intellectual_disability": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder": 1,
    "Inborn_genetic_diseases|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_specified|MECP2-related_disorder|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 1,
    "Neurodevelopmental_delay|Rett_syndrome": 1,
    "not_specified|not_provided|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "Rett_syndrome|not_provided|not_specified|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|not_specified|not_provided|Rett_syndrome": 2,
    "Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|MECP2-related_disorder": 2,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|History_of_neurodevelopmental_disorder|not_specified|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_specified": 1,
    "not_provided|Rett_syndrome|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|not_specified": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|MECP2-related_disorder|Rett_syndrome": 2,
    "Inborn_genetic_diseases|MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 2,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "History_of_neurodevelopmental_disorder|not_specified|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "not_specified|Rett_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|Intellectual_disability": 1,
    "not_provided|Neurodevelopmental_disorder|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_provided|Angelman_syndrome|Neurodevelopmental_delay|See_cases|Intellectual_disability": 1,
    "Focal_epilepsy|Rett_syndrome": 1,
    "MECP2-related_disorder|Rett_syndrome": 1,
    "MECP2-related_disorder|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|Rett_syndrome": 1,
    "Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome": 1,
    "History_of_neurodevelopmental_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|not_provided|not_specified": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|See_cases": 1,
    "MECP2-related_disorder|not_specified|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided|Microcephaly|Intellectual_disability|Psychomotor_retardation|Severe_underweight_in_infancy_childhood_and_adolescence": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Inborn_genetic_diseases": 1,
    "MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Inborn_genetic_diseases": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|History_of_neurodevelopmental_disorder|MECP2-related_disorder": 1,
    "MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Inborn_genetic_diseases|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_provided|not_specified|MECP2-related_disorder|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Inborn_genetic_diseases|not_specified|not_provided": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome|MECP2-related_disorder|not_specified": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|not_provided": 4,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Inborn_genetic_diseases|Rett_syndrome": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|MECP2-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|not_provided|MECP2-related_disorder|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|Encephalopathy|_neonatal_severeMental_retardation|_X-linked|_syndromic_13Rett_syndrome|not_provided|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|not_specified|not_provided|Autism|_susceptibility_to|_X-linked_3|See_cases": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|not_provided": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|not_specified": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 1,
    "not_provided|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly": 2,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|Neurodevelopmental_delay|Abnormality_of_the_nervous_system": 1,
    "Cone-rod_dystrophy|Inborn_genetic_diseases": 1,
    "not_provided|Rett_syndrome|MECP2-related_disorder|Seizure|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|History_of_neurodevelopmental_disorder|not_provided|not_specified|Rett_syndrome": 1,
    "not_provided|Rett_syndrome|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 2,
    "MECP2-related_disorder|History_of_neurodevelopmental_disorder|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|MECP2-related_disorder|Inborn_genetic_diseases|not_specified": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Rett_syndrome|MECP2-related_disorder": 1,
    "not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Rett_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 3,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome": 1,
    "MECP2-related_disorder|Rett_syndrome|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_provided|History_of_neurodevelopmental_disorder|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_specified": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Intellectual_disability": 1,
    "not_provided|History_of_neurodevelopmental_disorder|not_specified|MECP2-related_disorder|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome": 2,
    "MECP2-related_disorder|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Absent_speech|Developmental_regression|Severe_global_developmental_delay|Irregular_respiration|Seizure|Intellectual_disability": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|not_specified": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "MECP2-related_disorder|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome": 1,
    "Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|MECP2-related_disorder|not_specified": 1,
    "not_specified|MECP2-related_disorder|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified": 1,
    "Schizophrenia|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Rett_syndrome": 1,
    "Rett_syndrome|not_specified|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified": 1,
    "History_of_neurodevelopmental_disorder|MECP2-related_disorder|not_specified|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "Inborn_genetic_diseases|MECP2-related_disorder|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|not_provided": 1,
    "not_specified|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Inborn_genetic_diseases": 2,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|not_provided|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "MECP2-related_disorder|not_specified|Rett_syndrome": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder": 1,
    "Inborn_genetic_diseases|Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|not_provided": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Rett_syndrome|MECP2-related_disorder": 1,
    "MECP2-related_disorder|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "Inborn_genetic_diseases|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Rett_syndrome": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Encephalopathy|_neonatal_severeMental_retardation|_X-linked|_syndromic_13Rett_syndrome": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|Intellectual_disability|Global_developmental_delay|Developmental_regression": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|See_cases": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder": 2,
    "Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|MECP2-related_disorder": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|Angelman_syndrome|Abnormality_of_the_nervous_system|Neurodevelopmental_delay": 1,
    "Rett_syndrome|Inborn_genetic_diseases|not_provided": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "MECP2-related_disorder|not_provided|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|_zappella_variant": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Atypical_Rett_syndrome|Inborn_genetic_diseases|Rett_syndrome|Angelman_syndrome": 1,
    "MECP2-related_disorder|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Neurodevelopmental_disorder|Inborn_genetic_diseases|not_provided|Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3|Intellectual_disability|Microcephaly|Hearing_impairment|Stenosis_of_the_external_auditory_canal|Postnatal_growth_retardation|Downslanted_palpebral_fissures|Micrognathia|Motor_delay|Atypical_behavior": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Rett_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|not_provided": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Rett_syndrome|Inborn_genetic_diseases": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome|_zappella_variant|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Angelman_syndrome|Neurodevelopmental_delay|Intellectual_disability": 1,
    "Rett_syndrome|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|Rett_syndrome|not_provided": 1,
    "Rett_syndrome|not_provided|Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|MECP2-related_disorder|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Autism|_susceptibility_to|_X-linked_3": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|not_provided|Rett_syndrome|not_specified": 1,
    "Rett_syndrome|not_provided|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 2,
    "Inborn_genetic_diseases|not_specified|not_provided|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Autism|_susceptibility_to|_X-linked_3|not_provided|Rett_syndrome": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome": 1,
    "Bruxism|Delayed_speech_and_language_development|Stereotypic_movement_disorder|Delayed_gross_motor_development|Rett_syndrome|not_provided": 1,
    "Rett_syndrome|Global_developmental_delay|Metatarsus_adductus|Generalized_hypotonia": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|History_of_neurodevelopmental_disorder|not_provided": 1,
    "Syndromic_X-linked_intellectual_disability_Lubs_type|Rett_syndrome": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases|not_specified|not_provided|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|Angelman_syndrome": 1,
    "Rett_syndrome|not_provided|Autism|_susceptibility_to|_X-linked_3|Syndromic_X-linked_intellectual_disability_Lubs_type|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|MECP2-related_disorder|not_specified|Rett_syndrome": 1,
    "Rett_syndrome|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|Inborn_genetic_diseases": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome|MECP2-related_disorder|History_of_neurodevelopmental_disorder|not_specified|Syndromic_X-linked_intellectual_disability_Lubs_type|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|MECP2-related_disorder": 1,
    "Abnormality_of_the_nervous_system|Rett_syndrome": 1,
    "Inborn_genetic_diseases|Severe_neonatal-onset_encephalopathy_with_microcephaly|Autism|_susceptibility_to|_X-linked_3": 1,
    "Rett_syndrome|Angelman_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|not_specified|MECP2-related_disorder|Inborn_genetic_diseases|not_provided|Rett_syndrome": 1,
    "not_provided|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|Rett_syndrome": 1,
    "MECP2-related_disorder|Inborn_genetic_diseases": 1,
    "not_provided|Inborn_genetic_diseases|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Abnormal_muscle_fiber_morphology|Motor_neuron_atrophy|Progressive_neurologic_deterioration|Abnormal_synaptic_transmission|Central_hypotonia|Stridor|Congenital_laryngomalacia|Bulbar_palsy|Dystonic_disorder|Sick_sinus_syndrome|Central_apnea|Facial_hypertrichosis": 1,
    "Intellectual_disability|Rett_syndrome": 1,
    "Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Angelman_syndrome|not_provided|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided|Rett_syndrome": 1,
    "not_provided|Autism|_susceptibility_to|_X-linked_3|Rett_syndrome": 1,
    "MECP2-related_disorder|not_provided|Rett_syndrome|See_cases": 1,
    "Inborn_genetic_diseases|Rett_syndrome": 1,
    "Inborn_genetic_diseases|not_provided|Rett_syndrome": 1,
    "not_provided|MECP2-related_disorder|Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|MECP2-related_disorder|not_specified|not_provided|Rett_syndrome|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Syndromic_X-linked_intellectual_disability_Lubs_type|Severe_neonatal-onset_encephalopathy_with_microcephaly": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Inborn_genetic_diseases|Rett_syndrome|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|Syndromic_X-linked_intellectual_disability_Lubs_type|Autism|_susceptibility_to|_X-linked_3|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|Rett_syndrome|not_provided|MECP2-related_disorder|Inborn_genetic_diseases": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_specified|MECP2-related_disorder|Rett_syndrome": 1,
    "MECP2-related_disorder|Rett_syndrome|not_specified|Severe_neonatal-onset_encephalopathy_with_microcephaly|not_provided": 1,
    "X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_provided": 1,
    "Severe_neonatal-onset_encephalopathy_with_microcephaly|X-linked_intellectual_disability-psychosis-macroorchidism_syndrome|not_specified|Rett_syndrome": 1,
    "Cone_monochromatism": 3,
    "not_provided|Cone_monochromatism": 3,
    "RED_CONE_POLYMORPHISM|not_specified|not_provided": 1,
    "not_provided|Cone_monochromatism|Protan_defect": 1,
    "Protan_defect": 2,
    "Deuteranomaly": 4,
    "Cone_dystrophy_5|_X-linked": 1,
    "Cone_monochromatism|Deuteranomaly": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided": 15,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 280,
    "Developmental_delay|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome": 131,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 126,
    "not_specified|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant": 80,
    "Frontometaphyseal_dysplasia_1": 5,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Abnormality_of_neuronal_migration|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 301,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 4,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 144,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 228,
    "Heterotopia|_periventricular|_X-linked_dominant": 55,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 37,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 27,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 39,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 75,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 9,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_provided": 8,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_provided": 5,
    "FLNA-related_disorder|Cardiac_valvular_dysplasia|_X-linked|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 18,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 3,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 37,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 8,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 6,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 140,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 15,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|not_specified": 3,
    "not_provided|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Connective_tissue_disorder|not_specified|Frontometaphyseal_dysplasia": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 14,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 38,
    "FLNA-related_disorder": 50,
    "not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 8,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 6,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FLNA-related_disorder": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_provided|FG_syndrome_2": 1,
    "not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 7,
    "Dysplastic_corpus_callosum|Patent_foramen_ovale|Patent_ductus_arteriosus": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 16,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 14,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided": 16,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 5,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Melnick-Needles_syndrome|not_provided|Frontometaphyseal_dysplasia": 1,
    "Cardiovascular_phenotype|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 4,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 4,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Intellectual_disability": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 10,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "Thrombocytopenia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 10,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 7,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "not_provided|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 15,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 2,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 27,
    "not_specified|not_provided|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 5,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 34,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 4,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 8,
    "not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 17,
    "FLNA-related_disorder|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "Macrothrombocytopenia|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 22,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_specified|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 6,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|not_specified": 2,
    "not_specified|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|not_specified": 1,
    "not_provided|See_cases|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 12,
    "HETEROTOPIA|_PERIVENTRICULAR_NODULAR|_X-LINKED|_WITH_FRONTOMETAPHYSEAL_DYSPLASIA": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_provided": 12,
    "FG_syndrome_2": 7,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 12,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Connective_tissue_disorder|not_specified|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 14,
    "not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 6,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|not_provided": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder": 1,
    "not_specified|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder": 3,
    "Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified": 19,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 5,
    "Congenital_heart_disease|not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 13,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_provided": 2,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|not_specified": 2,
    "Oto-palato-digital_syndrome|_type_II": 3,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_specified": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 7,
    "not_provided|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 5,
    "Vascular_dilatation|Arterial_thrombosis|Arterial_tortuosity": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 3,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 3,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided": 8,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 2,
    "not_specified|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 2,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_provided": 3,
    "not_specified|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "not_provided|Thrombocytopenia|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|not_specified": 2,
    "not_specified|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 5,
    "not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 14,
    "Melnick-Needles_syndrome|not_provided": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Intellectual_disability": 1,
    "Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|not_specified": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 3,
    "Hearing_impairment|Heart|_malformation_of|Thrombocytopenia|Flexion_contracture": 1,
    "Macrothrombocytopenia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder": 1,
    "See_cases|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant": 2,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 1,
    "FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Cardiac_valvular_dysplasia|_X-linked|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|not_specified|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 4,
    "Cardiac_valvular_dysplasia|_X-linked": 13,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_provided": 1,
    "not_provided|not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 2,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Ehlers-Danlos_syndrome": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 13,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_provided": 1,
    "Attenuated_frontometaphyseal_dysplasia": 2,
    "not_specified|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 3,
    "Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 2,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|FLNA-related_disorder|Connective_tissue_disorder": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 3,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 4,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_provided": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Connective_tissue_disorder": 2,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_I": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 7,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Frontometaphyseal_dysplasia_1|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FLNA-related_disorder": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia_1": 1,
    "not_specified|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 6,
    "not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Wolff-Parkinson-White_pattern|not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "not_specified|not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 2,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Marfan_syndrome": 1,
    "FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Scoliosis": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 3,
    "not_specified|not_provided|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant": 2,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant": 5,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 2,
    "Connective_tissue_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thrombocytopenia|Abnormal_bleeding": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Hereditary_breast_ovarian_cancer_syndrome": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 2,
    "not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|not_specified": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_provided": 2,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|not_provided": 1,
    "not_provided|FLNA-related_disorder": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|FG_syndrome_2|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 2,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 3,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|See_cases|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided": 1,
    "Intellectual_disability|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Inborn_genetic_diseases": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Oto-palato-digital_syndrome|_type_I": 5,
    "not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Intellectual_disability|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_provided": 1,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 3,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Macrothrombocytopenia": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia_1|Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2|Frontometaphyseal_dysplasia": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome": 3,
    "FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 3,
    "FLNA-related_disorder|not_provided|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|See_cases": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 4,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_provided|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 1,
    "Melnick-Needles_syndrome": 5,
    "Otopalatodigital_syndrome_spectrum_disorder": 2,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_I": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 1,
    "not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 12,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_provided": 3,
    "Intellectual_disability|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "FLNA-related_disorder|not_provided": 2,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided|FLNA-related_disorder": 1,
    "FLNA-related_disorder|not_specified|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 2,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified": 3,
    "FLNA-related_disorder|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 1,
    "not_specified|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Intellectual_disability|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "FG_syndrome_2|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Frontometaphyseal_dysplasia": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Oto-palato-digital_syndrome|_type_I": 2,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 1,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Sudden_unexplained_death_in_childhood": 1,
    "not_provided|Cardiac_valvular_dysplasia|_X-linked": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|FG_syndrome_2|Melnick-Needles_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Frontometaphyseal_dysplasia_1|not_provided": 1,
    "not_provided|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 3,
    "FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Cardiac_valvular_dysplasia|_X-linked|not_provided": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder": 1,
    "not_specified|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified|not_provided": 1,
    "not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder": 1,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 2,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "Cardiac_valvular_dysplasia|_X-linked|See_cases|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_specified|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder": 2,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|not_specified|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 1,
    "Connective_tissue_disorder|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Thrombocytopenia|Aortic_dilatation": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1": 2,
    "not_specified|not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Cardiac_valvular_dysplasia|_X-linked|not_provided": 1,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "FLNA-related_disorder|not_specified|not_provided|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant": 4,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified": 3,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|not_specified|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Aortic_aneurysm|_familial_thoracic_2": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided": 2,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Ventricular_septal_defect|Intellectual_disability|_severe|Abnormality_of_the_dentition|Hydronephrosis|Myopia|Microcephaly|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Cardiac_valvular_dysplasia|_X-linked|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Connective_tissue_disorder|not_specified|not_provided": 1,
    "not_specified|not_provided|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Periventricular_nodular_heterotopia": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia_1|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder": 3,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia_1": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "FLNA-related_disorder|not_specified|not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|not_specified": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Cardiac_valvular_dysplasia|_X-linked": 2,
    "not_specified|not_provided|Oto-palato-digital_syndrome|_type_II|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Connective_tissue_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2": 1,
    "Cardiac_valvular_dysplasia|_X-linked|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 2,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_I|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder": 1,
    "not_provided|Melnick-Needles_syndrome": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Oto-palato-digital_syndrome|_type_I|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|FG_syndrome_2|Cardiac_valvular_dysplasia|_X-linked|not_provided": 1,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_specified|Connective_tissue_disorder": 1,
    "not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 2,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_specified": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_provided": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Connective_tissue_disorder|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Frontometaphyseal_dysplasia_1|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified|not_provided|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_specified": 1,
    "not_specified|not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided": 3,
    "FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome": 2,
    "not_provided|FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 1,
    "not_specified|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_II": 3,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_provided|Connective_tissue_disorder": 2,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FLNA-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified": 1,
    "Connective_tissue_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FG_syndrome_2|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|not_provided|Frontometaphyseal_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 1,
    "FG_syndrome_2|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided": 2,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 3,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|FLNA-related_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified": 2,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|FLNA-related_disorder": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Frontometaphyseal_dysplasia_1|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2": 1,
    "Intellectual_disability|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia_1": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Patent_ductus_arteriosus|Global_developmental_delay|Abnormality_of_the_face|Ventral_hernia|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Connective_tissue_disorder|Disorder_of_sexual_differentiation|Ehlers-Danlos_syndrome|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome": 3,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Frontometaphyseal_dysplasia_1|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|not_provided": 2,
    "not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 1,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia|not_provided": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder": 1,
    "Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder|FLNA-related_disorder": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Frontometaphyseal_dysplasia_1|FG_syndrome_2|FLNA-related_disorder|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "not_provided|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome": 2,
    "FLNA_related_lung_disease": 2,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Hepatoblastoma": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Neurodevelopmental_delay": 1,
    "not_specified|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Cardiac_valvular_dysplasia|_X-linked": 1,
    "FLNA-related_periventricular_nodular_heterotopia|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|FLNA-related_disorder|not_provided|Cardiac_valvular_dysplasia|_X-linked": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_specified": 1,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 1,
    "Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Connective_tissue_disorder": 1,
    "Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Melnick-Needles_syndrome|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|not_provided|Myopathy|_centronuclear|_2|Frontometaphyseal_dysplasia": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Microcephaly|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "not_provided|Connective_tissue_disorder|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_specified": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_I|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Frontometaphyseal_dysplasia": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|Connective_tissue_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|See_cases": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked": 1,
    "not_provided|FG_syndrome_2|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified": 2,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2|Melnick-Needles_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided": 1,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_specified|not_provided": 2,
    "not_specified|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Inborn_genetic_diseases|not_provided": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FLNA-related_disorder": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "FLNA-related_disorder|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|not_provided": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome": 1,
    "not_provided|not_specified|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Connective_tissue_disorder|FLNA-related_disorder|not_provided": 1,
    "not_specified|Connective_tissue_disorder|not_provided|Oto-palato-digital_syndrome|_type_II|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|not_specified": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|FLNA-related_disorder|Connective_tissue_disorder": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 2,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 2,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Oto-palato-digital_syndrome|_type_I|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|FLNA-related_disorder|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 2,
    "Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II": 2,
    "not_specified|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder": 1,
    "not_provided|Periventricular_nodular_heterotopia": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_specified|Ehlers-Danlos_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_provided": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder|Cardiac_valvular_dysplasia|_X-linked|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Oto-palato-digital_syndrome|_type_I|FG_syndrome_2|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Frontometaphyseal_dysplasia_1|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|not_specified|FLNA-related_disorder|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_specified": 1,
    "Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia_1|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|FG_syndrome_2|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Melnick-Needles_syndrome|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Cardiac_valvular_dysplasia|_X-linked|FG_syndrome_2|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|not_provided|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Cardiac_valvular_dysplasia|_X-linked": 1,
    "not_provided|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified|not_provided": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder|not_specified|not_provided|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome": 1,
    "not_provided|Frontometaphyseal_dysplasia_1|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|FLNA-related_disorder": 1,
    "FLNA-related_otopalatodigital_spectrum_disorders": 1,
    "not_specified|FLNA-related_disorder|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "Cardiac_valvular_dysplasia|_X-linked|not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "not_specified|not_provided|FLNA-related_disorder|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II": 1,
    "HETEROTOPIA|_PERIVENTRICULAR_NODULAR|_X-LINKED_DOMINANT|_WITH_MELNICK-NEEDLES_SYNDROME": 1,
    "Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_specified|not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_I|Conductive_hearing_impairment|Cleft_palate|Short_stature": 1,
    "Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_provided|Oto-palato-digital_syndrome|_type_I": 1,
    "Hypotonia|Congenital_omphalocele|Orofacial_cleft|Ambiguous_genitalia": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FG_syndrome_2|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Cardiac_valvular_dysplasia|_X-linked|Frontometaphyseal_dysplasia_1|Melnick-Needles_syndrome": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "Oto-palato-digital_syndrome|_type_II|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Melnick-Needles_syndrome|Cardiac_valvular_dysplasia|_X-linked|Oto-palato-digital_syndrome|_type_I|Oto-palato-digital_syndrome|_type_II|FG_syndrome_2|Heterotopia|_periventricular|_X-linked_dominant|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Frontometaphyseal_dysplasia_1|Frontometaphyseal_dysplasia|not_provided": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Cardiac_valvular_dysplasia|_X-linked|Otopalatodigital_Spectrum_Disorders": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|not_provided|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection": 1,
    "not_specified|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_provided|Cardiac_valvular_dysplasia|_X-linked": 1,
    "FLNA-related_disorder|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|not_specified": 1,
    "Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|not_specified": 1,
    "Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|not_specified|FLNA-related_disorder": 1,
    "Terminal_osseous_dysplasia-pigmentary_defects_syndrome": 1,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Heterotopia|_periventricular|_X-linked_dominant|Oto-palato-digital_syndrome|_type_II|not_provided": 1,
    "Melnick-Needles_syndrome|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked|Terminal_osseous_dysplasia-pigmentary_defects_syndrome|Oto-palato-digital_syndrome|_type_II|Oto-palato-digital_syndrome|_type_I|Cardiac_valvular_dysplasia|_X-linked|Frontometaphyseal_dysplasia_1|Heterotopia|_periventricular|_X-linked_dominant|FG_syndrome_2": 1,
    "not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|FLNA-related_disorder": 1,
    "Frontometaphyseal_dysplasia|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant": 1,
    "Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Connective_tissue_disorder|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided": 1,
    "not_provided|Heterotopia|_periventricular|_X-linked_dominant|Neurodevelopmental_delay": 1,
    "Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Connective_tissue_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_specified|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia": 1,
    "not_provided|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|FLNA-related_disorder|not_specified": 1,
    "Oto-palato-digital_syndrome|_type_II|Frontometaphyseal_dysplasia|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|not_specified|Familial_thoracic_aortic_aneurysm_and_aortic_dissection|not_provided|FLNA-related_disorder": 1,
    "Familial_thoracic_aortic_aneurysm_and_aortic_dissection|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Melnick-Needles_syndrome|Frontometaphyseal_dysplasia|not_specified|FLNA-related_disorder": 1,
    "FLNA-related_disorder|not_provided|Melnick-Needles_syndrome|Oto-palato-digital_syndrome|_type_II|Heterotopia|_periventricular|_X-linked_dominant|Frontometaphyseal_dysplasia": 1,
    "CONGENITAL_SHORT_BOWEL_SYNDROME|_X-LINKED|Intestinal_pseudoobstruction|_neuronal|_chronic_idiopathic|_X-linked": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|EMD-related_disorder|not_provided": 1,
    "EMD-related_disorder": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided": 17,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked": 14,
    "X-linked_Emery-Dreifuss_muscular_dystrophy": 309,
    "Cardiomyopathy|EMD-related_disorder|X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "Primary_dilated_cardiomyopathy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy": 23,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 21,
    "not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy": 6,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 2,
    "not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_specified|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 3,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Charcot-Marie-Tooth_disease_type_2": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|X-linked_Emery-Dreifuss_muscular_dystrophy": 5,
    "not_provided|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_provided|Cardiovascular_phenotype|not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy": 2,
    "Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 3,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_provided": 1,
    "not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 13,
    "Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided": 2,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy": 5,
    "not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 4,
    "not_specified|EMD-related_disorder|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|Cardiomyopathy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy": 9,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "not_provided|not_specified|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy": 1,
    "Myopathy|Flexion_contracture|Failure_to_thrive": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified": 6,
    "not_provided|not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|EMD-related_disorder|Emery-Dreifuss_muscular_dystrophy_1|_X-linked": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Neuromuscular_disease|not_provided|Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|not_specified": 1,
    "EMD-related_disorder|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_1|_X-linked": 2,
    "Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|Cardiovascular_phenotype|not_provided": 1,
    "not_provided|Cardiovascular_phenotype|Cardiomyopathy|EMD-related_disorder|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified|Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_specified|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 2,
    "not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|not_provided": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_1|_X-linked": 1,
    "Cardiovascular_phenotype|not_specified|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiomyopathy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|not_specified|Cardiomyopathy|not_provided": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_specified|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 2,
    "Cardiovascular_phenotype|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 2,
    "not_provided|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "not_provided|Cardiomyopathy|not_specified|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|not_provided|EMD-related_disorder|Cardiovascular_phenotype": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_specified|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 3,
    "Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified": 1,
    "EMD-related_disorder|Emery-Dreifuss_muscular_dystrophy|not_provided|not_specified|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|Cardiovascular_phenotype|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided|Cardiovascular_phenotype": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "not_specified|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided|Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|not_specified|Cardiovascular_phenotype": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided|not_specified|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|not_provided|Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype": 1,
    "Cardiovascular_phenotype|not_provided|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Cardiovascular_phenotype|not_provided|Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided|Cardiovascular_phenotype": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|Neuromuscular_disease|not_provided|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "Cardiovascular_phenotype|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy|not_specified|not_provided": 1,
    "Emery-Dreifuss_muscular_dystrophy_1|_X-linked|not_provided|Emery-Dreifuss_muscular_dystrophy|X-linked_Emery-Dreifuss_muscular_dystrophy": 1,
    "X-linked_Emery-Dreifuss_muscular_dystrophy|Emery-Dreifuss_muscular_dystrophy_1|_X-linked|Cardiovascular_phenotype|not_provided": 1,
    "Intellectual_disability|_X-linked|_syndromic|_35|not_provided": 4,
    "Intellectual_disability|_X-linked|_syndromic|_35": 7,
    "Intellectual_disability|_X-linked|_syndromic|_35|Autism|_susceptibility_to|_X-linked_5": 1,
    "not_provided|Intellectual_disability|_X-linked|_syndromic|_35": 2,
    "RPL10-related_disorder": 2,
    "Autism|_susceptibility_to|_X-linked_5": 1,
    "Autism|_susceptibility_to|_X-linked_5|not_provided": 1,
    "Endocardial_fibroelastosis|Dilated_cardiomyopathy_3B|Left_ventricular_noncompaction_cardiomyopathy|3-Methylglutaconic_aciduria_type_2": 1,
    "not_provided|Endocardial_fibroelastosis|Primary_dilated_cardiomyopathy|Left_ventricular_noncompaction_cardiomyopathy|3-Methylglutaconic_aciduria_type_2": 1,
    "3-Methylglutaconic_aciduria_type_2": 319,
    "Cardiovascular_phenotype|not_specified|not_provided|3-Methylglutaconic_aciduria_type_2": 2,
    "Cardiovascular_phenotype|3-Methylglutaconic_aciduria_type_2": 18,
    "not_provided|3-Methylglutaconic_aciduria_type_2|Left_ventricular_noncompaction_cardiomyopathy": 1,
    "3-Methylglutaconic_aciduria_type_2|Cardiovascular_phenotype": 17,
    "Cardiovascular_phenotype|not_specified|3-Methylglutaconic_aciduria_type_2": 1,
    "3-Methylglutaconic_aciduria_type_2|Endocardial_fibroelastosis|Primary_dilated_cardiomyopathy": 1,
    "3-Methylglutaconic_aciduria_type_2|Cardiovascular_phenotype|not_provided": 4,
    "3-Methylglutaconic_aciduria_type_2|not_provided": 13,
    "not_provided|3-Methylglutaconic_aciduria_type_2": 18,
    "not_specified|not_provided|3-Methylglutaconic_aciduria_type_2": 2,
    "not_provided|3-Methylglutaconic_aciduria_type_2|not_specified|Cardiomyopathy": 1,
    "3-Methylglutaconic_aciduria_type_2|not_specified": 6,
    "3-Methylglutaconic_aciduria_type_2|Caused_by_mutation_in_the_tafazzin_gene|not_provided": 1,
    "3-Methylglutaconic_aciduria_type_2|not_specified|Cardiovascular_phenotype": 1,
    "TAFAZZIN-related_disorder|3-Methylglutaconic_aciduria_type_2": 2,
    "3-Methylglutaconic_aciduria_type_2|Primary_dilated_cardiomyopathy|Endocardial_fibroelastosis": 3,
    "not_provided|3-Methylglutaconic_aciduria_type_2|Cardiovascular_phenotype": 3,
    "not_specified|3-Methylglutaconic_aciduria_type_2|Cardiovascular_phenotype": 1,
    "3-Methylglutaconic_aciduria_type_2|Cardiomyopathy": 2,
    "Primary_dilated_cardiomyopathy|3-Methylglutaconic_aciduria_type_2": 2,
    "not_provided|3-Methylglutaconic_aciduria_type_2|Primary_dilated_cardiomyopathy|Endocardial_fibroelastosis|TAFAZZIN-related_disorder": 1,
    "not_specified|3-Methylglutaconic_aciduria_type_2": 4,
    "not_provided|3-Methylglutaconic_aciduria_type_2|TAFAZZIN-related_disorder|Cardiomyopathy": 1,
    "Primary_dilated_cardiomyopathy|Cardiovascular_phenotype|Left_ventricular_noncompaction_cardiomyopathy|3-Methylglutaconic_aciduria_type_2|not_specified|Endocardial_fibroelastosis|not_provided": 1,
    "Primary_dilated_cardiomyopathy|Endocardial_fibroelastosis|Left_ventricular_noncompaction_cardiomyopathy|3-Methylglutaconic_aciduria_type_2|not_provided": 2,
    "Primary_dilated_cardiomyopathy|3-Methylglutaconic_aciduria_type_2|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Endocardial_fibroelastosis": 1,
    "3-Methylglutaconic_aciduria_type_2|not_specified|not_provided": 1,
    "TAFAZZIN-related_disorder|Cardiovascular_phenotype|3-Methylglutaconic_aciduria_type_2": 1,
    "TAFAZZIN-related_disorder|not_provided|3-Methylglutaconic_aciduria_type_2": 2,
    "3-Methylglutaconic_aciduria_type_2|not_specified|Cardiovascular_phenotype|not_provided": 1,
    "3-Methylglutaconic_aciduria_type_2|Primary_dilated_cardiomyopathy|not_specified|not_provided|Endocardial_fibroelastosis": 1,
    "Primary_dilated_cardiomyopathy|3-Methylglutaconic_aciduria_type_2|Endocardial_fibroelastosis": 3,
    "3-Methylglutaconic_aciduria_type_2|Primary_dilated_cardiomyopathy": 2,
    "3-Methylglutaconic_aciduria_type_2|Dilated_cardiomyopathy_1A": 1,
    "TAFAZZIN-related_disorder|Cardiovascular_phenotype|not_specified|not_provided|3-Methylglutaconic_aciduria_type_2": 1,
    "Cardiovascular_phenotype|3-Methylglutaconic_aciduria_type_2|not_provided": 1,
    "Left_ventricular_noncompaction_cardiomyopathy|Primary_dilated_cardiomyopathy|not_provided|Endocardial_fibroelastosis|3-Methylglutaconic_aciduria_type_2|not_specified|Cardiomyopathy|Cardiovascular_phenotype": 1,
    "3-Methylglutaconic_aciduria_type_2|TAFAZZIN-related_disorder": 1,
    "3-Methylglutaconic_aciduria_type_2|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "not_provided|3-Methylglutaconic_aciduria_type_2|not_specified|Cardiovascular_phenotype": 1,
    "not_provided|not_specified|3-Methylglutaconic_aciduria_type_2|Cardiovascular_phenotype": 1,
    "not_provided|3-Methylglutaconic_aciduria_type_2|Cardiomyopathy": 1,
    "Cardiovascular_phenotype|Primary_dilated_cardiomyopathy|3-Methylglutaconic_aciduria_type_2|not_provided|Endocardial_fibroelastosis": 1,
    "3-Methylglutaconic_aciduria_type_2|Cardiovascular_phenotype|not_specified": 1,
    "not_provided|Cardiovascular_phenotype|3-Methylglutaconic_aciduria_type_2": 1,
    "Cardiomyopathy|3-Methylglutaconic_aciduria_type_2": 1,
    "not_provided|Cardiovascular_phenotype|TAFAZZIN-related_disorder|3-Methylglutaconic_aciduria_type_2": 1,
    "Endocardial_fibroelastosis|Cardiovascular_phenotype|3-Methylglutaconic_aciduria_type_2|not_provided|Left_ventricular_noncompaction_cardiomyopathy|Primary_dilated_cardiomyopathy|not_specified": 1,
    "Primary_dilated_cardiomyopathy|Endocardial_fibroelastosis|Left_ventricular_noncompaction_cardiomyopathy|3-Methylglutaconic_aciduria_type_2": 2,
    "Endocardial_fibroelastosis|Left_ventricular_noncompaction_cardiomyopathy|3-Methylglutaconic_aciduria_type_2|Primary_dilated_cardiomyopathy": 1,
    "not_provided|ATP6AP1-related_disorder": 2,
    "not_provided|ATP6AP1-related_disorder|ALG2-congenital_disorder_of_glycosylation": 1,
    "ATP6AP1-related_disorder|not_provided": 2,
    "not_provided|Immunodeficiency_47": 5,
    "Immunodeficiency_47|not_provided": 6,
    "Immunodeficiency_47": 14,
    "ATP6AP1-related_disorder": 2,
    "not_provided|ATP6AP1-related_disorder|Intellectual_disability": 1,
    "not_provided|Decreased_total_lymphocyte_count|Decreased_total_neutrophil_count|Immunodeficiency_47": 1,
    "Immunodeficiency_47|ATP6AP1-related_disorder": 1,
    "Inborn_genetic_diseases|Immunodeficiency_47|not_provided": 1,
    "Intellectual_disability|_X-linked_41": 19,
    "Inborn_genetic_diseases|GDI1-related_disorder|not_specified|not_provided": 1,
    "not_specified|Intellectual_disability|_X-linked_41|Immunodeficiency_47": 1,
    "GDI1-related_disorder": 4,
    "not_provided|Intellectual_disability|_X-linked_41|Inborn_genetic_diseases|not_specified": 1,
    "not_specified|Intellectual_disability|_X-linked_41": 1,
    "Intellectual_disability|_X-linked_41|Inborn_genetic_diseases|not_provided|not_specified": 1,
    "Intellectual_disability|_X-linked_41|not_provided": 1,
    "not_provided|GDI1-related_disorder|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_41|Inborn_genetic_diseases": 1,
    "Intellectual_disability|_X-linked_41|Intellectual_disability": 1,
    "not_provided|Intellectual_disability|_X-linked_41": 1,
    "FAM50A-related_disorder|Armfield_syndrome": 1,
    "Armfield_syndrome": 1,
    "FAM50A-related_disorder": 3,
    "Armfield_syndrome|not_provided": 4,
    "not_provided|Armfield_syndrome": 1,
    "Armfield_syndrome|Intellectual_disability": 1,
    "PLXNA3-related_disorder": 436,
    "PLXNA3-related_disorder|not_provided": 21,
    "not_specified|PLXNA3-related_disorder": 79,
    "PLXNA3-related_disorder|Short_stature|not_specified": 1,
    "PLXNA3-related_disorder|not_specified": 27,
    "not_provided|PLXNA3-related_disorder": 36,
    "not_provided|PLXNA3-related_disorder|not_specified": 4,
    "not_specified|Autism|Microtia": 1,
    "PLXNA3-associated_seizure_disorder": 1,
    "PLXNA3-related_disorder|Childhood-onset_schizophrenia": 1,
    "PLXNA3-related_neurodevelopmental_disorder": 1,
    "not_provided|not_specified|PLXNA3-related_disorder": 2,
    "Galloway-Mowat_syndrome_2|_X-linked|not_provided": 1,
    "Galloway-Mowat_syndrome_2|_X-linked": 11,
    "not_provided|LAGE3-related_disorder": 3,
    "LAGE3-related_disorder|not_specified": 2,
    "LAGE3-related_disorder|not_provided|Galloway-Mowat_syndrome_2|_X-linked": 1,
    "LAGE3-related_disorder": 6,
    "LAGE3-related_disorder|not_provided": 2,
    "not_specified|not_provided|Galloway-Mowat_syndrome_2|_X-linked": 1,
    "not_provided|LAGE3-related_disorder|not_specified": 1,
    "not_specified|LAGE3-related_disorder|not_provided": 1,
    "G6PD_deficiency": 13,
    "G6PD_deficiency|not_provided": 2,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency|not_provided": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 523,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided": 19,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency": 7,
    "not_specified|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 7,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 21,
    "G6PD_SPLIT|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD-related_disorder|not_specified|not_provided|G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD_NEAPOLIS|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Inborn_genetic_diseases|Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_KAIPING|G6PD_ANANT|G6PD_DHON|G6PD_deficiency|G6PD_PETRICH-LIKE|G6PD_SAPPORO-LIKE": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to": 6,
    "G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 8,
    "G6PD-related_disorder|Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_GIFU|G6PD_AGRIGENTO|G6PD_TAIWAN-HAKKA|G6PD_CANTON|G6PD_deficiency": 1,
    "not_provided|G6PD_COSENZA|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency|Malaria|_susceptibility_to": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 3,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Inborn_genetic_diseases": 1,
    "not_specified|not_provided|G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 3,
    "G6PD_ANDALUS|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_deficiency": 1,
    "Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_SANTIAGO_DE_CUBA": 1,
    "not_provided|G6PD_PAWNEE|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_specified": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_VARNSDORF": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_ZURICH": 1,
    "not_specified|not_provided|G6PD-related_disorder|G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD-related_disorder": 1,
    "G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD-related_disorder": 1,
    "G6PD_JAPAN|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_RIVERSIDE": 1,
    "G6PD_ALHAMBRA|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_NASHVILLE|G6PD_ANAHEIM|G6PD_PORTICI|not_specified|not_provided": 1,
    "G6PD_BEVERLY_HILLS|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_GUADALAJARA": 1,
    "G6PD-related_disorder|G6PD_WALTER_REED|G6PD_IOWA|G6PD_IOWA_CITY|G6PD_SPRINGFIELD|not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD_TOMAH|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD-related_disorder": 2,
    "not_provided|not_specified|G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_PUERTO_LIMON|not_provided": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Decreased_glucosephosphate_isomerase_level|Hemolytic_anemia": 1,
    "Inborn_genetic_diseases|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 2,
    "G6PD_LOMA_LINDA|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_SERRES": 1,
    "G6PD_IERAPETRA|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency": 1,
    "Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 4,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_deficiency|G6PD_MAHIDOL-LIKE": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|Inborn_genetic_diseases|not_provided|G6PD_CHATHAM": 1,
    "G6PD-related_disorder": 7,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_deficiency": 1,
    "G6PD_REHOVOT|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD-related_disorder|not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Congenital_nonspherocytic_hemolytic_anemia|Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_deficiency|G6PD_KERALA|G6PD_KALYAN|G6PD_KERALA-KALYAN": 1,
    "G6PD_deficient_hemolytic_anemia|G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|Inborn_genetic_diseases|not_provided|G6PD_VIANGCHAN|G6PD_JAMMU|G6PD_deficiency": 1,
    "not_provided|G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_specified": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_MODENA|G6PD_deficiency|G6PD_SEATTLE-LIKE": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency|Malaria|_susceptibility_to": 1,
    "G6PD_AVEIRO|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Inborn_genetic_diseases|not_specified|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_MEXICO_CITY|not_specified|G6PD_deficiency": 1,
    "G6PD_HARILAOU|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided": 1,
    "not_specified|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_GASTONIA|G6PD_MARION|G6PD_MINNESOTA|See_cases": 1,
    "Malaria|_susceptibility_to|not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_SANTIAGO": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|G6PD_NILGIRI": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|G6PD_COIMBRA": 1,
    "not_provided|G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Hemolytic_anemia|_G6PD_deficient_(favism)|Inborn_genetic_diseases|G6PD_deficient_hemolytic_anemia|G6PD-related_disorder|Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_MEDITERRANEAN|G6PD_SASSARI|G6PD_CAGLIARI|G6PD_deficiency|See_cases": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency|G6PD_MALAGA|Malaria|_susceptibility_to": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|G6PD_NANKANG": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|G6PD_TAIWAN-HAKKA_2|not_provided|not_specified": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_MAHIDOL|G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|not_specified": 2,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_deficiency": 1,
    "not_specified|not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_ILESHA": 1,
    "Malaria|_susceptibility_to|Familial_hemolytic_anemia|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to": 2,
    "G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|Malaria|_susceptibility_to": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_QUING_YUAN": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency|Malaria|_susceptibility_to": 1,
    "G6PD_deficiency|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Inborn_genetic_diseases|Malaria|_susceptibility_to|not_specified|not_provided|Glomerulopathy_with_fibronectin_deposits_2|G6PD_A+": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|Malaria|_susceptibility_to": 1,
    "not_provided|G6PD_NAMORU|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_deficiency|Inborn_genetic_diseases|not_specified|not_provided|G6PD_ASAHI|Malaria|_susceptibility_to": 1,
    "G6PD_METAPONTO|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_specified": 1,
    "not_provided|not_specified|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency": 1,
    "G6PD-related_disorder|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_deficiency|G6PD_AURES": 1,
    "Malaria|_susceptibility_to|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|not_provided|G6PD_deficiency|G6PD_ORISSA": 1,
    "Incontinentia_pigmenti_syndrome": 6,
    "Ectodermal_dysplasia_and_immunodeficiency_1|Immunodeficiency_33|Incontinentia_pigmenti_syndrome|Autoinflammatory_disease|_X-linked|Anhidrotic_ectodermal_dysplasia-immunodeficiency-osteopetrosis-lymphedema_syndrome": 1,
    "IKBKG-related_disorder": 4,
    "IKBKG-related_disorder|Ectodermal_dysplasia_and_immunodeficiency_1": 1,
    "not_specified|IKBKG-related_disorder|not_provided": 1,
    "not_provided|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|G6PD_SUNDERLAND": 1,
    "Inborn_genetic_diseases|Anemia|_nonspherocytic_hemolytic|_due_to_G6PD_deficiency|Malaria|_susceptibility_to|not_provided|G6PD_deficiency|G6PD_GAOHE|Early-onset_coronary_artery_disease": 1,
    "G6PD-related_disorder|not_provided": 1,
    "Immunodeficiency_33": 7,
    "Autoinflammatory_disease|_X-linked": 3,
    "Autoinflammatory_disease|_X-linked|Ectodermal_dysplasia_and_immunodeficiency_1|Immunodeficiency_33|Incontinentia_pigmenti_syndrome": 1,
    "Immunodeficiency_33|Ectodermal_dysplasia_and_immunodeficiency_1|Incontinentia_pigmenti_syndrome|Autoinflammatory_disease|_X-linked|IKBKG-related_disorder|Common_variable_immunodeficiency|not_provided": 1,
    "Incontinentia_pigmenti_syndrome|not_provided": 3,
    "Inborn_genetic_diseases|not_specified|not_provided|Ectodermal_dysplasia_and_immunodeficiency_1": 1,
    "Ectodermal_dysplasia_and_immunodeficiency_1": 9,
    "not_provided|Ectodermal_dysplasia_and_immunodeficiency_1|Immunodeficiency_33": 1,
    "Ectodermal_dysplasia_and_immunodeficiency_1|Immunodeficiency_33": 1,
    "Ectodermal_dysplasia_and_immunodeficiency_1|not_provided": 3,
    "Immunodeficiency_33|not_provided": 2,
    "Incontinentia_pigmenti_syndrome|IMMUNODEFICIENCY_33|_MALE-RESTRICTED": 1,
    "NEMO_deleted_exon_5-autoinflammatory_syndrome_(NEMO-NDAS)": 1,
    "Incontinentia_pigmenti_syndrome|not_specified": 1,
    "Autoinflammatory_disease|_X-linked|not_provided": 1,
    "not_provided|Autoinflammatory_disease|_X-linked": 1,
    "Immunodeficiency_33|Ectodermal_dysplasia_and_immunodeficiency_1|Autoinflammatory_disease|_X-linked|Incontinentia_pigmenti_syndrome|not_provided": 1,
    "not_provided|Ectodermal_dysplasia_and_immunodeficiency_1": 3,
    "not_provided|Ectodermal_dysplasia_and_immunodeficiency_1|not_specified": 1,
    "not_provided|Incontinentia_pigmenti_syndrome": 2,
    "ECTODERMAL_DYSPLASIA_AND_IMMUNODEFICIENCY_1|_MALE-RESTRICTED|Incontinentia_pigmenti_syndrome": 1,
    "not_provided|ECTODERMAL_DYSPLASIA_AND_IMMUNODEFICIENCY_1|_MALE-RESTRICTED|Incontinentia_pigmenti_syndrome": 1,
    "Immunodeficiency_33|not_provided|Incontinentia_pigmenti_syndrome|Ectodermal_dysplasia_and_immunodeficiency_1": 1,
    "ECTODERMAL_DYSPLASIA_AND_IMMUNODEFICIENCY_1|_MALE-RESTRICTED|Ectodermal_dysplasia_and_immunodeficiency_1|Incontinentia_pigmenti_syndrome": 1,
    "Incontinentia_pigmenti_syndrome|ECTODERMAL_DYSPLASIA_AND_IMMUNODEFICIENCY_1|_MALE-RESTRICTED": 1,
    "DKC1-related_disorder|not_specified|not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked": 8,
    "DKC1-related_disorder": 4,
    "DKC1-related_disorder|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|_X-linked|Dyskeratosis_congenita": 4,
    "not_provided|Dyskeratosis_congenita|DKC1-related_disorder|not_specified": 1,
    "Dyskeratosis_congenita|DKC1-related_disorder": 10,
    "Hoyeraal-Hreidarsson_syndrome|Dyskeratosis_congenita|_X-linked": 1,
    "not_provided|Dyskeratosis_congenita|_X-linked|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_X-linked|not_provided|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked|Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1": 1,
    "DKC1-related_disorder|Dyskeratosis_congenita": 1,
    "Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1|Dyskeratosis_congenita|_X-linked": 3,
    "Dyskeratosis_congenita|_X-linked|Hoyeraal-Hreidarsson_syndrome|not_provided|Dyskeratosis_congenita": 1,
    "not_provided|not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked": 1,
    "not_provided|Dyskeratosis_congenita|_X-linked": 2,
    "Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1": 1,
    "Hoyeraal-Hreidarsson_syndrome": 1,
    "DKC1-related_disorder|not_provided|not_specified|Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|DKC1-related_disorder|not_specified|not_provided": 1,
    "not_provided|Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|Congenital_cerebellar_hypoplasia|Dyskeratosis_congenita|_X-linked|not_provided": 1,
    "not_provided|DKC1-related_disorder": 1,
    "Dyskeratosis_congenita|Dyskeratosis_congenita|_X-linked|not_provided": 1,
    "Dyskeratosis_congenita|_X-linked|Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1|Dyskeratosis_congenita|Hoyeraal-Hreidarsson_syndrome": 1,
    "Dyskeratosis_congenita|_X-linked|Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1|Dyskeratosis_congenita": 1,
    "not_provided|Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1|Dyskeratosis_congenita|_X-linked|not_specified|Dyskeratosis_congenita": 1,
    "Dyskeratosis_congenita|_X-linked|not_provided": 1,
    "not_provided|DKC1-related_disorder|Dyskeratosis_congenita|not_specified": 1,
    "not_provided|DKC1-related_disorder|History_of_neurodevelopmental_disorder|Dyskeratosis_congenita|not_specified": 1,
    "Dyskeratosis_congenita|not_specified|not_provided|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|DKC1-related_disorder|not_specified|not_provided|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|Cataracts|_hearing_impairment|_nephrotic_syndrome|_and_enterocolitis_1|Dyskeratosis_congenita|_X-linked": 1,
    "Dyskeratosis_congenita|_X-linked|not_specified|not_provided": 1,
    "Hereditary_factor_VIII_deficiency_disease|not_provided": 37,
    "Hemophilia_A|_FVIII_Deficiency": 1,
    "Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease|not_provided": 7,
    "not_provided|Hereditary_factor_VIII_deficiency_disease": 34,
    "Hereditary_factor_IX_deficiency_disease|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect": 8,
    "Hereditary_factor_VIII_deficiency_disease|Abnormality_of_coagulation": 1,
    "F8-related_disorder|Hereditary_factor_VIII_deficiency_disease|not_provided": 1,
    "Inborn_genetic_diseases|Hereditary_factor_VIII_deficiency_disease": 5,
    "Hereditary_factor_VIII_deficiency_disease|not_specified": 4,
    "Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_specified|not_provided": 1,
    "F8-related_disorder": 32,
    "Hereditary_factor_VIII_deficiency_disease|not_specified|Inborn_genetic_diseases": 1,
    "Hereditary_factor_VIII_deficiency_disease|Hereditary_factor_IX_deficiency_disease": 4,
    "Hereditary_factor_VIII_deficiency_disease|See_cases|F8-related_disorder": 1,
    "Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided": 7,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease": 9,
    "Hereditary_factor_VIII_deficiency_disease|not_specified|F8-related_disorder": 1,
    "Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided|Hereditary_factor_IX_deficiency_disease": 1,
    "not_provided|Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect": 2,
    "not_provided|F8-related_disorder": 5,
    "Hereditary_factor_VIII_deficiency_disease|not_provided|Hereditary_factor_IX_deficiency_disease": 1,
    "Inborn_genetic_diseases|Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided|Hereditary_factor_IX_deficiency_disease|F8-related_disorder": 1,
    "not_provided|Thrombophilia|_X-linked|_due_to_factor_8_defect": 2,
    "Hereditary_factor_VIII_deficiency_disease|not_provided|Thrombophilia|_X-linked|_due_to_factor_8_defect": 1,
    "not_specified|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided": 1,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect": 7,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided|Inborn_genetic_diseases|Hereditary_factor_VIII_deficiency_disease": 1,
    "not_provided|F8-related_disorder|Hereditary_factor_VIII_deficiency_disease": 3,
    "not_specified|Thrombophilia|_X-linked|_due_to_factor_8_defect": 1,
    "not_specified|F8-related_disorder": 1,
    "Abnormal_bleeding|Hereditary_factor_VIII_deficiency_disease": 1,
    "Hereditary_factor_VIII_deficiency_disease|Inborn_genetic_diseases": 1,
    "Cerebral_palsy|Hereditary_factor_VIII_deficiency_disease": 1,
    "not_specified|not_provided|Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect": 1,
    "F8-related_disorder|not_provided|Hereditary_factor_VIII_deficiency_disease|Abnormality_of_coagulation": 1,
    "not_provided|Hereditary_factor_VIII_deficiency_disease|FACTOR_VIII_(EAST_HARTFORD)": 1,
    "Hereditary_factor_VIII_deficiency_disease|Inborn_genetic_diseases|not_provided": 1,
    "Hereditary_factor_VIII_deficiency_disease|Inborn_genetic_diseases|not_specified": 1,
    "Hereditary_factor_VIII_deficiency_disease|not_specified|not_provided": 2,
    "Hereditary_factor_VIII_deficiency_disease|F8-related_disorder|not_provided": 1,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease|not_provided": 2,
    "Hereditary_factor_VIII_deficiency_disease|F8-related_disorder|not_specified": 1,
    "not_specified|Hereditary_factor_VIII_deficiency_disease|not_provided": 2,
    "Hereditary_factor_VIII_deficiency_disease|Interstitial_lung_disease_due_to_ABCA3_deficiency": 1,
    "not_provided|F8-related_disorders": 1,
    "F8-related_disorder|not_provided": 2,
    "F8-related_disorder|not_specified|Hereditary_factor_VIII_deficiency_disease": 1,
    "Inborn_genetic_diseases|not_provided|Hereditary_factor_VIII_deficiency_disease": 2,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|not_specified|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "Inborn_genetic_diseases|F8-related_disorder": 2,
    "F8-related_disorder|not_specified": 1,
    "not_provided|Inborn_genetic_diseases|Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease": 1,
    "F8-related_disorder|Inborn_genetic_diseases": 1,
    "not_specified|Hereditary_factor_VIII_deficiency_disease|F8-related_disorder": 1,
    "F8-related_disorder|Hereditary_factor_VIII_deficiency_disease": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease|not_provided": 1,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease|not_provided|Hereditary_factor_IX_deficiency_disease|Abnormality_of_coagulation": 1,
    "not_provided|Mild_hemophilia_A|Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease": 1,
    "F8-related_disorder|Hereditary_factor_VIII_deficiency_disease|not_specified|not_provided": 1,
    "not_provided|Familial_aortopathy|Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect": 1,
    "F8-related_disorder|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "Mild_hemophilia_A|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "not_provided|Hereditary_factor_VIII_deficiency_disease|Hereditary_factor_IX_deficiency_disease": 1,
    "Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_specified": 1,
    "F8-related_disorder|not_provided|Thrombophilia|_X-linked|_due_to_factor_8_defect|Hereditary_factor_VIII_deficiency_disease": 1,
    "Hereditary_factor_VIII_deficiency_disease|F8-related_disorder": 4,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided|Hereditary_factor_VIII_deficiency_disease": 1,
    "not_specified|Hereditary_factor_VIII_deficiency_disease": 4,
    "not_provided|Hereditary_factor_IX_deficiency_disease|FACTOR_VIII_(OKAYAMA)|Hereditary_factor_VIII_deficiency_disease": 1,
    "F8-related_disorder|not_specified|Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease|not_provided": 1,
    "Hereditary_factor_VIII_deficiency_disease|not_specified|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided": 1,
    "Hereditary_factor_VIII_deficiency_disease|not_provided|F8-related_disorder|Thrombophilia|_X-linked|_due_to_factor_8_defect": 1,
    "F8-related_disorder|Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease": 1,
    "Hereditary_factor_IX_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|not_provided": 1,
    "not_provided|Hereditary_factor_VIII_deficiency_disease|Abnormality_of_coagulation": 1,
    "Hereditary_factor_IX_deficiency_disease|Hereditary_factor_VIII_deficiency_disease|not_provided|F8-related_disorder": 1,
    "Hereditary_factor_VIII_deficiency_disease|Thrombophilia|_X-linked|_due_to_factor_8_defect|Hemorrhage|F8-related_disorder|not_provided": 1,
    "Hereditary_factor_VIII_deficiency_disease|not_specified|Thrombophilia|_X-linked|_due_to_factor_8_defect": 1,
    "not_provided|not_specified|F8-related_disorder|Inborn_genetic_diseases": 1,
    "Thrombophilia|_X-linked|_due_to_factor_8_defect|not_specified|Hereditary_factor_VIII_deficiency_disease": 1,
    "Intellectual_disability|_X-linked_72": 30,
    "not_provided|Intellectual_disability|_X-linked_72": 4,
    "Intellectual_disability|_X-linked_72|not_provided": 2,
    "Parkinson_disease|_X-linked_dominant": 2,
    "Early-onset_parkinsonism-intellectual_disability_syndrome|Parkinson_disease|_X-linked_dominant": 1,
    "Inborn_genetic_diseases|not_specified|not_provided|Intellectual_disability|_X-linked_72|RAB39B-related_disorder": 1,
    "Early-onset_parkinsonism-intellectual_disability_syndrome|not_provided": 1,
    "Intellectual_disability|_X-linked_72|Early-onset_parkinsonism-intellectual_disability_syndrome": 2,
    "not_provided|Intellectual_disability|_X-linked_72|Early-onset_parkinsonism-intellectual_disability_syndrome": 1,
    "RAB39B-related_disorder|not_provided|Inborn_genetic_diseases": 1,
    "Inborn_genetic_diseases|not_provided|RAB39B-related_disorder|Early-onset_parkinsonism-intellectual_disability_syndrome": 1,
    "Early-onset_parkinsonism-intellectual_disability_syndrome": 1,
    "RAB39B-related_disorder|Inborn_genetic_diseases": 1,
    "X-linked_intellectual_disability-cardiomegaly-congestive_heart_failure_syndrome": 4,
    "not_specified|X-linked_intellectual_disability-cardiomegaly-congestive_heart_failure_syndrome": 1,
    "CLIC2-related_disorder": 1,
    "X-linked_intellectual_disability-cardiomegaly-congestive_heart_failure_syndrome|not_specified": 1,
    "Epsilon-trimethyllysine_hydroxylase_deficiency|not_specified": 1,
    "Epsilon-trimethyllysine_hydroxylase_deficiency": 8,
    "TMLHE-related_disorder": 5,
    "not_provided|Epsilon-trimethyllysine_hydroxylase_deficiency": 1,
    "not_specified|not_provided|TMLHE-related_disorder": 1,
    "not_specified|Epsilon-trimethyllysine_hydroxylase_deficiency": 2,
    "not_specified|Epsilon-trimethyllysine_hydroxylase_deficiency|not_provided": 1,
    "Epsilon-trimethyllysine_hydroxylase_deficiency|not_provided|not_specified": 1,
    "Congenital_cerebellar_hypoplasia|Cerebellar_vermis_hypoplasia|Corpus_callosum|_agenesis_of": 1,
    "Epsilon-trimethyllysine_hydroxylase_deficiency|not_provided|Intellectual_disability": 1,
    "not_provided|VAMP7-related_disorder": 1,
    "VAMP7-related_disorder": 1,
    "Turner_syndrome": 1,
    "46|XY_sex_reversal_1": 47,
    "46|XY_sex_reversal_1|not_provided": 1,
    "46|XX_sex_reversal_1|46|XY_sex_reversal_1": 1,
    "46|XX_sex_reversal_1": 1,
    "SRY-related_disorder": 3,
    "46|XY_TRUE_HERMAPHRODITISM|46|XY_sex_reversal_1": 1,
    "not_provided|46|XY_sex_reversal_1": 1,
    "Deafness|_Y-linked_2": 1,
    "TBL1Y-related_disorder": 2,
    "not_provided|Deafness|_Y-linked_2|TBL1Y-related_disorder": 1,
    "Spermatogenic_failure|_Y-linked|_2": 8,
    "USP9Y-related_disorder": 2,
    "DDX3Y-related_disorder": 1,
    "Venous_thromboembolism": 3,
    "Leber_optic_atrophy|Mitochondrial_inheritance": 3,
    "Mitochondrial_inheritance|MELAS_syndrome": 1,
    "Mitochondrial_disease|MELAS_syndrome": 28,
    "MELAS_syndrome|Mitochondrial_disease": 10,
    "Mitochondrial_disease|Mitochondrial_encephalopathy|MELAS_syndrome": 1,
    "Hypomagnesemia|Hypokalemia|Nephropathy|_chronic_tubulointerstitial|Mitochondrial_disease": 1,
    "not_specified|Mitochondrial_disease|Interstitial_nephritis": 1,
    "MERRF_syndrome": 3,
    "Interstitial_nephritis|Mitochondrial_disease|MELAS_syndrome|Epilepsy|_mitochondrial": 1,
    "Epilepsy|_mitochondrial": 1,
    "Mitochondrial_disease|Myopathy|_mitochondrial|_late-onset": 1,
    "MELAS_syndrome|not_specified": 6,
    "MELAS_syndrome|Hypokalemia|Hypomagnesemia|Chronic_kidney_disease": 1,
    "not_provided|not_specified|Venous_thromboembolism": 1,
    "Gentamicin_response|Aminoglycoside-induced_deafness|Mitochondrial_non-syndromic_sensorineural_hearing_loss": 1,
    "Mitochondrial_non-syndromic_sensorineural_hearing_loss|not_specified": 1,
    "Rare_genetic_deafness|Mitochondrial_disease": 1,
    "Aminoglycoside-induced_deafness|streptomycin_response_-_Toxicity|gentamicin_response_-_Toxicity|aminoglycoside_antibacterials_response_-_Toxicity|kanamycin_response_-_Toxicity|Mitochondrial_non-syndromic_sensorineural_hearing_loss|not_provided|Auditory_neuropathy|not_specified": 1,
    "Mitochondrial_non-syndromic_sensorineural_hearing_loss|not_provided": 1,
    "Gentamicin_response|Aminoglycoside-induced_deafness|kanamycin_response_-_Toxicity|streptomycin_response_-_Toxicity|tobramycin_response_-_Toxicity|gentamicin_response_-_Toxicity|aminoglycoside_antibacterials_response_-_Toxicity|Mitochondrial_disease|Mitochondrial_non-syndromic_sensorineural_hearing_loss|Rare_genetic_deafness|Aminoglycoside_Ototoxicity": 1,
    "Mitochondrial_non-syndromic_sensorineural_hearing_loss|Aminoglycoside-induced_deafness|gentamicin_response_-_Toxicity|amikacin_response_-_Toxicity|aminoglycoside_antibacterials_response_-_Toxicity|kanamycin_response_-_Toxicity|streptomycin_response_-_Toxicity|tobramycin_response_-_Toxicity|Aminoglycoside_induced_ototoxicity|Rare_genetic_deafness|Gentamicin_response|Hearing_loss|_sensorineural|_autosomal-mitochondrial_type|Mitochondrial_disease|Restrictive_cardiomyopathy|not_provided": 1,
    "Mitochondrial_disease|Ataxia|_progressive_seizures|_mental_deterioration|_and_hearing_loss|MELAS_syndrome": 1,
    "Mitochondrial_disease|MELAS_syndrome|not_provided": 2,
    "Mitochondrial_disease|Leigh_syndrome|Leigh_syndrome|_mitochondrial|MELAS_syndrome": 1,
    "not_specified|MELAS_syndrome": 13,
    "MELAS_syndrome|not_provided": 6,
    "Epilepsy|Hyperlactaemia|Developmental_delay|Axial_hypotonia": 1,
    "not_specified|Mitochondrial_disease|Charcot-Marie-Tooth_disease|_axonal|_mitochondrial_form|_1|Spastic_paraplegia|_mitochondrial|Epilepsy|Hyperlactaemia|Developmental_delay|Axial_hypotonia": 1,
    "Mitochondrial_inheritance": 3,
    "Chloramphenicol_resistance": 2,
    "Mitochondrial_disease|Myelodysplastic_syndrome|MELAS_syndrome": 1,
    "Leigh_syndrome|_mitochondrial|Glucose_intolerance|Short_stature|Sensorineural_hearing_loss_disorder|Stroke_disorder|Maternally-inherited_mitochondrial_myopathy|Charcot-Marie-Tooth_disease|_axonal|_mitochondrial_form|_1|Hypertrophic_cardiomyopathy|MELAS_syndrome|Diabetes-deafness_syndrome_maternally_transmitted|Leigh_Syndrome_(mtDNA_mutation)|Auditory_neuropathy_spectrum_disorder|not_specified|MERRF_syndrome|not_provided|Mitochondrial_disease|3-methylglutaconic_aciduria_type_1|Cyclical_vomiting_syndrome|Age_related_macular_degeneration_2|Leigh_syndrome|MERRF/MELAS_overlap_syndrome|Cerebral_palsy|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|See_cases": 1,
    "Kearns-Sayre_syndrome|Mitochondrial_disease": 1,
    "Mitochondrial_skeletal_myopathy|_responsive_to_riboflavin|MELAS_syndrome": 1,
    "MELAS_syndrome|Progressive_external_ophthalmoplegia|_proximal_myopathy|_and_sudden_death|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Mitochondrial_encephalomyopathy|MELAS_syndrome": 1,
    "Diabetes_mellitus|_noninsulin-dependent|_maternally_transmitted|MERRF_syndrome|MELAS_syndrome|Mitochondrial_disease": 1,
    "MITOCHONDRIAL_CARDIOMYOPATHY_WITH_OR_WITHOUT_SKELETAL_MYOPATHY|MELAS_syndrome|Mitochondrial_disease": 1,
    "MELAS_syndrome|Mitochondrial_disease|not_specified|MERRF_syndrome": 1,
    "Neuropsychiatric_disorder_and_early-onset_cataract|Mitochondrial_disease|MERRF_syndrome|MELAS_syndrome": 1,
    "Developmental_delay|Leber_optic_atrophy|MELAS_syndrome|Fibrosis|Hepatitis|Hepatic_steatosis|Myopia|Neuromuscular_disease": 1,
    "MELAS_syndrome|SUDDEN_INFANT_DEATH_SYNDROME": 1,
    "Mitochondrial_disease|MELAS_syndrome|MITOCHONDRIAL_CARDIOMYOPATHY_WITH_OR_WITHOUT_SKELETAL_MYOPATHY|MITOCHONDRIAL_SKELETAL_MYOPATHY": 1,
    "MELAS_syndrome|Mitochondrial_disease|MITOCHONDRIAL_CARDIOMYOPATHY_WITH_OR_WITHOUT_SKELETAL_MYOPATHY": 1,
    "Leigh_syndrome|not_specified|SUDDEN_INFANT_DEATH_SYNDROME|Carcinoma_of_colon": 1,
    "SUDDEN_INFANT_DEATH_SYNDROME|Leigh_syndrome": 1,
    "not_provided|Mitochondrial_disease|Leigh_syndrome": 4,
    "Leber_optic_atrophy|Mitochondrial_disease": 10,
    "Leigh_syndrome|not_provided|Mitochondrial_non-syndromic_sensorineural_hearing_loss|Optic_atrophy": 1,
    "not_provided|Leber_optic_atrophy|Optic_atrophy|Mitochondrial_disease|Leigh_syndrome": 1,
    "Parkinson_disease|_late-onset|Leigh_syndrome|Alzheimer_disease": 1,
    "Leber_optic_atrophy|not_provided|MELAS_syndrome|Leigh_syndrome|MITOCHONDRIAL_COMPLEX_I_DEFICIENCY|_MITOCHONDRIAL_TYPE_3|Optic_atrophy|Mitochondrial_disease": 1,
    "Leigh_syndrome|Mitochondrial_disease|MELAS_syndrome": 1,
    "Mitochondrial_disease|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|MELAS_syndrome": 1,
    "Intellectual_disability|Leigh_syndrome": 1,
    "Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|Mitochondrial_disease": 3,
    "not_provided|Global_developmental_delay|Generalized_hypotonia": 1,
    "Leigh_syndrome|Ptosis|Abnormal_CSF_lactate_concentration|Increased_circulating_lactate_concentration|Abnormality_of_eye_movement|Gait_disturbance|Dysarthria": 1,
    "Mitochondrial_disease|Leigh_syndrome": 17,
    "Attention_deficit_hyperactivity_disorder|Migraine|Hypertonia|Seizure|Ventriculomegaly|Developmental_regression|Dystonic_disorder|Leber_optic_atrophy_and_dystonia|MELAS_syndrome|Leber_optic_atrophy|Mitochondrial_disease": 1,
    "Leber_optic_atrophy|Optic_neuropathy|Visual_loss|Abnormal_electroretinogram|Mitochondrial_disease": 1,
    "See_cases|Mitochondrial_disease": 1,
    "not_provided|Dystonia|_adult-onset|Leigh_syndrome|not_specified": 1,
    "Leigh_syndrome|See_cases": 2,
    "not_specified|Mitochondrial_disease|Leigh_syndrome": 2,
    "Mitochondrial_disease|MITOCHONDRIAL_COMPLEX_I_DEFICIENCY|_MITOCHONDRIAL_TYPE_3": 1,
    "Leber_optic_atrophy|MELAS_syndrome|Mitochondrial_disease|Leigh_syndrome": 1,
    "not_provided|Leber_optic_atrophy|Leigh_syndrome": 1,
    "Mitochondrial_disease|not_provided|Leigh_syndrome": 3,
    "Leber_optic_atrophy|not_provided|Leigh_syndrome": 1,
    "Leigh_syndrome|not_provided|not_specified|Leber_optic_atrophy": 1,
    "Mitochondrial_disease|Cardiomyopathy|_fatal": 1,
    "Progressive_external_ophthalmoplegia": 3,
    "not_specified|not_provided|MELAS_syndrome": 1,
    "MELAS_syndrome|Multisystem_disorder|Mitochondrial_disease|not_provided|MERRF_syndrome": 1,
    "MELAS_syndrome|Encephalopathy|_familial_progressive_necrotizing": 1,
    "Mitochondrial_disease|Hypomagnesemia|_hypertension|_and_hypercholesterolemia|_mitochondrial": 1,
    "not_specified|not_provided|Mitochondrial_non-syndromic_sensorineural_hearing_loss|Primary_familial_hypertrophic_cardiomyopathy|MELAS_syndrome|Mitochondrial_disease": 1,
    "MERRF_syndrome|MELAS_syndrome": 1,
    "Primary_dilated_cardiomyopathy|Asymmetric_septal_hypertrophy|Hypomagnesemia|_hypertension|_and_hypercholesterolemia|_mitochondrial|Mitochondrial_disease|Primary_familial_hypertrophic_cardiomyopathy|MERRF_syndrome": 1,
    "Cardiomyopathy|_fatal_infantile|MELAS_syndrome": 1,
    "MELAS_syndrome|MT-TQ-related_myopathy|Mitochondrial_disease": 1,
    "MELAS_syndrome|not_provided|not_specified|Mitochondrial_disease|Sensorineural_deafness_and_migraine": 1,
    "MELAS_syndrome|not_specified|not_provided": 1,
    "not_provided|MELAS_syndrome": 8,
    "Leber_optic_atrophy|Leigh_syndrome": 9,
    "Epilepsy|Developmental_delay": 1,
    "Mitochondrial_disease|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_disease": 1,
    "Leigh_syndrome|not_specified|Leber_optic_atrophy": 3,
    "Mitochondrial_disease|Mitochondrial_complex_I_deficiency": 1,
    "Mitochondrial_disease|Leber_optic_atrophy": 4,
    "Mitochondrial_disease|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency": 2,
    "New-onset_refractory_status_epilepticus": 1,
    "Inborn_mitochondrial_myopathy|not_provided|Mitochondrial_disease|MELAS_syndrome": 1,
    "Leigh_syndrome|Mitochondrial_disease": 3,
    "Neurogastrointestinal_syndrome|_mitochondrial|Mitochondrial_disease|MELAS_syndrome": 1,
    "Mitochondrial_encephalopathy|not_provided|Leigh_syndrome": 1,
    "Encephalocardiomyopathy|_mitochondrial|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Mitochondrial_encephalopathy": 1,
    "Mitochondrial_disease|Mitochondrial_encephalomyopathy": 1,
    "MELAS_syndrome|Leigh_syndrome": 3,
    "Mitochondrial_disease|not_provided|Inborn_mitochondrial_myopathy|MELAS_syndrome": 1,
    "Inborn_mitochondrial_myopathy|Mitochondrial_disease": 3,
    "Myotonic_dystrophy-like_myopathy|Mitochondrial_disease": 1,
    "External_ophthalmoplegia": 2,
    "Ophthalmoplegia|_isolated": 1,
    "Pure_mitochondrial_myopathy": 1,
    "External_ophthalmoplegia|Ptosis|Mitochondrial_disease": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease|Ophthalmoplegia|_isolated": 1,
    "MITOCHONDRIAL_COMPLEX_I_DEFICIENCY|_MITOCHONDRIAL_TYPE_2|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease|not_provided|MELAS_syndrome": 1,
    "Macrocytic_dyserythropoietic_anemia|Primary_dilated_cardiomyopathy": 2,
    "not_provided|MELAS_syndrome|Mitochondrial_disease": 1,
    "Dystonia|_mitochondrial|Mitochondrial_disease": 1,
    "Focal_segmental_glomerulosclerosis_and_dilated_cardiomyopathy|MELAS_syndrome": 1,
    "Exercise_intolerance_and_complex_III_deficiency|_somatic|not_provided|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Kearns-Sayre_syndrome": 3,
    "See_cases|MELAS_syndrome": 1,
    "Mitochondrial_disease|Myoglobinuria|_recurrent": 1,
    "Familial_colorectal_cancer|Leigh_syndrome": 2,
    "Cytochrome_c_oxidase_I_deficiency|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Leigh_syndrome|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Leigh_syndrome|not_specified|Cytochrome_c_oxidase_I_deficiency": 1,
    "Abnormal_mitral_valve_physiology": 10,
    "Abnormal_aortic_valve_physiology": 11,
    "Mitochondrial_disease|Myelodysplastic_syndrome_with_ring_sideroblasts": 1,
    "Mitochondrial_disease|Myelodysplastic_syndrome_with_ring_sideroblasts|not_specified": 1,
    "Tetralogy_of_Fallot|Abnormal_aortic_valve_physiology": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease": 3,
    "Mitochondrial_DNA-related_disorder|Leigh_syndrome": 1,
    "Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency": 3,
    "Mitochondrial_non-syndromic_sensorineural_hearing_loss|Mitochondrial_disease": 3,
    "Mitochondrial_non-syndromic_sensorineural_hearing_loss|Leigh_syndrome|Aminoglycoside-induced_deafness|not_provided|not_specified|Mitochondrial_disease|Leber_optic_atrophy": 1,
    "MELAS_syndrome|Mitochondrial_disease|Mitochondrial_non-syndromic_sensorineural_hearing_loss|Palmoplantar_keratoderma-deafness_syndrome": 1,
    "Mitochondrial_disease|Mitochondrial_non-syndromic_sensorineural_hearing_loss": 1,
    "neonatal_lactic_acidosis|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_non-syndromic_sensorineural_hearing_loss|Mitochondrial_disease|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Deafness|_sensorineural|_with_neurologic_features|Mitochondrial_disease|Rare_genetic_deafness|Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_cytochrome_c_oxidase_deficiency|Mitochondrial_non-syndromic_sensorineural_hearing_loss|MELAS_syndrome|MERRF_syndrome|not_provided": 1,
    "not_specified|MELAS_syndrome|Mitochondrial_disease": 1,
    "not_provided|MELAS_syndrome|not_specified": 2,
    "Mitochondrial_disease|MELAS_syndrome|not_specified": 1,
    "Myopathy|MELAS_syndrome": 1,
    "Mitochondrial_disease|MELAS_syndrome|Exercise_intolerance|_muscle_pain|_and_lactic_acidemia|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "not_specified|Mitochondrial_disease|MELAS_syndrome": 3,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_non-syndromic_sensorineural_hearing_loss|Mitochondrial_disease": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease|MELAS_syndrome|Mitochondrial_non-syndromic_sensorineural_hearing_loss": 1,
    "Limb_ataxia|Mitochondrial_disease|MELAS_syndrome|MERRF/MELAS_overlap_syndrome|Mitochondrial_cytochrome_c_oxidase_deficiency|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 1,
    "Mitochondrial_disease|Mitochondrial_myopathy|_isolated": 1,
    "not_specified|Leigh_syndrome|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Mitochondrial_complex_IV_deficiency|_nuclear_type_1": 4,
    "Leigh_syndrome|Decreased_activity_of_mitochondrial_complex_IV": 1,
    "Familial_colorectal_cancer|not_specified": 1,
    "Focal_white_matter_lesions|Ischemic_stroke|Leigh_syndrome": 1,
    "Mitochondrial_cytochrome_c_oxidase_deficiency": 1,
    "MELAS_syndrome|Mitochondrial_inheritance": 1,
    "Mitochondrial_disease|MELAS_syndrome|Diabetes-deafness_syndrome_maternally_transmitted": 1,
    "Mitochondrial_disease|Mitochondrial_DNA_depletion_syndrome_1": 1,
    "Mitochondrial_disease|MELAS_syndrome|Kearns-Sayre_syndrome": 1,
    "Mitochondrial_disease|Progressive_external_ophthalmoplegia_with_myoclonus|not_specified": 1,
    "MT-TK-related_disorder|MT-TK-related_mitochondrial_disorder|Complex_hereditary_spastic_paraplegia|not_provided|Mitochondrial_disease|Thrombocythemia_2|Parkinson_disease|_mitochondrial|MELAS_syndrome|Leigh_syndrome|MERRF_syndrome": 1,
    "Pearson_syndrome": 3,
    "MERRF/MELAS_overlap_syndrome|MELAS_syndrome|Mitochondrial_disease|MERRF_syndrome": 1,
    "MELAS_syndrome|Cardiomyopathy_and_Deafness|Mitochondrial_disease|Leigh_syndrome|MERRF_syndrome": 1,
    "Leigh_syndrome|Brain_pseudoatrophy|_reversible|_valproate-induced|_susceptibility_to": 1,
    "Mitochondrial_disease|Optic_neuropathy|not_specified": 1,
    "Bicuspid_aortic_valve": 2,
    "Cardiomyopathy|_infantile_hypertrophic|Mitochondrial_disease|Histiocytoid_cardiomyopathy": 1,
    "Mitochondrial_disease|Cardiomyopathy|_apical_hypertrophic|_and_neuropathy": 1,
    "Leigh_syndrome|Mitochondrial_disease|not_provided": 6,
    "Mitochondrial_disease|NARP_syndrome": 1,
    "Leigh_syndrome|_mitochondrial": 1,
    "Leber_optic_atrophy|NARP_syndrome|Mitochondrial_DNA-Associated_Leigh_Syndrome_and_NARP|Leigh_syndrome": 1,
    "Mitochondrial_disease|NARP_syndrome|Leigh_syndrome|Leber_optic_atrophy": 1,
    "not_provided|Mitochondrial_disease|Striatonigral_degeneration|_infantile|_mitochondrial|Leber_optic_atrophy|NARP_syndrome|Leigh_syndrome": 1,
    "Bicuspid_aortic_valve|Leigh_syndrome": 1,
    "Leber_optic_atrophy|Myopathy|_lactic_acidosis|_and_sideroblastic_anemia_3|Mitochondrial_disease|MELAS_syndrome|not_provided": 1,
    "Mitochondrial_DNA-Associated_Leigh_Syndrome_and_NARP|Leigh_syndrome": 2,
    "Mitochondrial_complex_5_(ATP_synthase)_deficiency|_mitochondrial_type_1|Ataxia_and_polyneuropathy|_adult-onset|Leber_optic_atrophy|NARP_syndrome|not_provided|Mitochondrial_disease|Leigh_syndrome": 1,
    "Cerebellar_ataxia|Mitochondrial_complex_5_(ATP_synthase)_deficiency|_mitochondrial_type_1|not_specified|not_provided|Mitochondrial_disease|NARP_syndrome|Leber_optic_atrophy|Striatonigral_degeneration|_infantile|_mitochondrial|Leigh_syndrome|Wide_intermamillary_distance|Premature_birth|Low-set_ears|Camptodactyly_of_finger|Postaxial_hand_polydactyly|Hypoplasia_of_scrotum|Bilateral_cleft_lip_and_palate|Hypertelorism|Rod-cone_dystrophy": 1,
    "NARP_syndrome": 1,
    "Mitochondrial_disease|NARP_syndrome|Leigh_syndrome|Cerebellar_ataxia|Cerebellar_atrophy|Tremor|Rod-cone_dystrophy": 1,
    "Progressive_cerebellar_ataxia|See_cases|MT-ATP6-related_primary_mitochondrial_disease|Mitochondrial_disease|NARP_syndrome|Leber_optic_atrophy|Leigh_syndrome": 1,
    "See_cases|Mitochondrial_disease|Leigh_syndrome": 1,
    "Gonadal_dysgenesis|Abnormal_basal_ganglia_MRI_signal_intensity|Progressive_spastic_paraparesis|Cerebellar_ataxia|Mitochondrial_disease|Leigh_syndrome": 1,
    "Leigh_syndrome|Mitochondrial_disease|not_specified": 1,
    "Leigh_syndrome|Peripheral_neuropathy": 1,
    "Mitochondrial_disease|Mitochondrial-DNA_disorder|not_provided|Leigh_syndrome": 1,
    "Leigh_syndrome|Optic_neuropathy|Mitochondrial_disease": 1,
    "Mitochondrial_complex_5_(ATP_synthase)_deficiency|_mitochondrial_type_1|Leigh_syndrome|_mitochondrial|Maternally-inherited_spastic_paraplegia|Striatonigral_degeneration|_infantile|_mitochondrial|Leber_optic_atrophy|not_provided|NARP_syndrome|Mitochondrial_disease|Leigh_syndrome": 1,
    "Mitochondrial_complex_5_(ATP_synthase)_deficiency|_mitochondrial_type_1|Leigh_syndrome|not_provided|Leber_optic_atrophy|Mitochondrial_disease": 1,
    "Mitochondrial_DNA-Associated_Leigh_Syndrome_and_NARP|not_provided|Charcot-Marie-Tooth_disease|_type_IA|Charcot-Marie-Tooth_disease|Leigh_syndrome|Mitochondrial_complex_5_(ATP_synthase)_deficiency|_mitochondrial_type_1|Mitochondrial_disease|Leber_optic_atrophy|NARP_syndrome": 1,
    "Leber_optic_atrophy|Mitochondrial_disease|Seizures_and_lactic_acidosis": 1,
    "Leber_optic_atrophy|Mitochondrial_encephalopathy|Epilepsy|Developmental_delay": 1,
    "Oromandibular_dystonia|Cerebellar_ataxia|Difficulty_walking|Hearing_impairment|Short_stature|Chronic_fatigue|Exercise_intolerance|Nephrolithiasis|Subcutaneous_lipoma|Moderate_sensorineural_hearing_impairment|Abnormal_mitochondria_in_muscle_tissue|Sleep_apnea|Acute_liver_failure": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency": 1,
    "Autosomal_dominant_spastic_ataxia|not_provided|not_specified|Leigh_syndrome": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease|Mitochondrial_complex_IV_deficiency_with_recurrent_myoglobinuria": 1,
    "Mitochondrial_complex_IV_deficiency|_nuclear_type_1|Mitochondrial_disease|Leigh_syndrome": 1,
    "Venous_thromboembolism|not_specified": 1,
    "not_specified|Leigh_syndrome|not_provided|Mitochondrial_disease|Leber_optic_atrophy|See_cases": 1,
    "not_specified|Mitochondrial_disease|Primary_familial_hypertrophic_cardiomyopathy": 1,
    "Exercise_intolerance|Mitochondrial_disease": 2,
    "Sudden_death|MELAS_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|_mitochondrial_type_1|not_provided|Mitochondrial_disease|Leigh_syndrome": 1,
    "Mitochondrial_complex_I_deficiency|Mitochondrial_complex_I_deficiency|_mitochondrial_type_1|Mitochondrial_disease|Leigh_syndrome": 1,
    "Mitochondrial_myopathy|_episodic|_with_optic_atrophy_and_reversible_leukoencephalopathy|Mitochondrial_complex_I_deficiency|_mitochondrial_type_1|not_specified|Mitochondrial_DNA-Associated_Leigh_Syndrome_and_NARP|not_provided|Mitochondrial_disease|Leber_optic_atrophy_and_dystonia|Leigh_syndrome|See_cases": 1,
    "Hereditary_optic_neuropathy": 1,
    "sensorimotor_axonal_polyneuropathy": 1,
    "Leigh_syndrome|not_specified|Parkinson_disease|_resistance_to|not_provided": 1,
    "Mitochondrial_encephalomyopathy|Mitochondrial_disease": 2,
    "Familial_colorectal_cancer|Mitochondrial_disease": 1,
    "Leigh_syndrome|not_provided|Mitochondrial_disease": 2,
    "Leigh_syndrome|Leber_optic_atrophy|not_specified": 1,
    "Seizure|Leigh_syndrome|Leber_optic_atrophy": 1,
    "Visual_impairment|Optic_atrophy|Optic_neuritis|Central_scotoma|Optic_neuropathy": 1,
    "Leber_optic_atrophy|Leigh_syndrome|Leber_optic_atrophy_and_dystonia": 1,
    "not_specified|Venous_thromboembolism": 1,
    "Mitochondrial_disease|Leber_optic_atrophy|Leber_optic_atrophy_and_dystonia|Leigh_syndrome|Mitochondrial_complex_I_deficiency": 1,
    "Leber_optic_atrophy_and_dystonia|Mitochondrial_disease|Leber_optic_atrophy|_susceptibility_to|not_specified|Leber_optic_atrophy|Optic_atrophy|Retinal_dystrophy|not_provided": 1,
    "Hypotonia|Dementia|Epilepsy|Developmental_delay|Encephalopathy|Calcification_of_extrapyramidal_basal_ganglia": 1,
    "Peripheral_neuropathy|Ataxia|Hearing_impairment": 1,
    "Dystonic_disorder|Developmental_delay": 1,
    "Leigh_syndrome|Macrocephaly|Developmental_delay|Hearing_impairment|Hypotonia|Dementia|Epilepsy|Encephalopathy|Calcification_of_extrapyramidal_basal_ganglia|Microcephaly|Congenital_cardiomyopathy": 1,
    "Seizure|Stroke_disorder": 1,
    "Leigh_syndrome|Hypotonia|Dementia|Epilepsy|Developmental_delay|Encephalopathy|Calcification_of_extrapyramidal_basal_ganglia|Microcephaly|Congenital_cardiomyopathy|Hearing_impairment|Macrocephaly": 1,
    "Leigh_syndrome|Intellectual_disability": 1,
    "MELAS_syndrome|MERRF/MELAS_overlap_syndrome|Mitochondrial_disease": 1,
    "mtDNA-related_disorders": 1,
    "PIGMENTARY_RETINOPATHY_AND_SENSORINEURAL_DEAFNESS|Mitochondrial_disease": 1,
    "MELAS_syndrome|MT-TH-related_condition": 1,
    "CARDIOMYOPATHY|_IDIOPATHIC_DILATED|_MITOCHONDRIAL|CARDIOMYOPATHY|_HYPERTROPHIC|_MITOCHONDRIAL|MELAS_syndrome": 1,
    "MELAS_syndrome|Mitochondrial_non-syndromic_sensorineural_hearing_loss|Mitochondrial_disease": 1,
    "MERRF/MELAS_overlap_syndrome|MELAS_syndrome|Mitochondrial_disease": 1,
    "not_provided|Mitochondrial_disease|MELAS_syndrome": 2,
    "See_cases|Mitochondrial_disease|MELAS_syndrome": 1,
    "Cerebellar_ataxia|_cataract|_and_diabetes_mellitus|Retinitis_pigmentosa-deafness_syndrome|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Diabetes-deafness_syndrome_maternally_transmitted|MELAS_syndrome": 1,
    "MELAS_syndrome|Cardiomyopathy|_mitochondrial|not_provided": 1,
    "MELAS_syndrome|Mitochondrial_encephalomyopathy|Mitochondrial_disease": 1,
    "not_specified|Mitochondrial_disease": 1,
    "Leigh_syndrome|Autosomal_recessive_early-onset_Parkinson_disease_6": 1,
    "Mitochondrial_disease|Mitochondrial_complex_V_(ATP_synthase)_deficiency|_nuclear_type_5|MELAS_syndrome|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|Leber_optic_atrophy": 1,
    "Leber_optic_atrophy|Leigh_syndrome|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|Mitochondrial_disease": 1,
    "not_provided|Leigh_syndrome|Leber_optic_atrophy|Mitochondrial_disease": 1,
    "Leber_optic_atrophy|MELAS_syndrome|Leigh_syndrome": 1,
    "Leber_optic_atrophy|Mitochondrial_disease|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|MERRF_syndrome|MELAS_syndrome": 1,
    "MELAS_syndrome|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|Mitochondrial_disease|Leber_optic_atrophy": 1,
    "Mitochondrial_disease|Leber_optic_atrophy|Leigh_syndrome": 1,
    "MELAS_syndrome|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Leigh_syndrome|_mitochondrial|Leber_optic_atrophy|MELAS_syndrome": 1,
    "not_provided|MELAS_syndrome|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|Leigh_syndrome|Mitochondrial_disease": 1,
    "Mitochondrial_disease|MELAS_syndrome|Leigh_syndrome": 1,
    "MELAS_syndrome|not_provided|Leigh_syndrome|Mitochondrial_disease": 1,
    "Leber_optic_atrophy|Leigh_syndrome|not_specified": 2,
    "Hearing_impairment|Congenital_cardiomyopathy|Microcephaly|Developmental_delay": 1,
    "Leigh_syndrome|MELAS_syndrome|Mitochondrial_DNA-Associated_Leigh_Syndrome_and_NARP|Leber_optic_atrophy": 1,
    "Oxyphilic_adenoma": 1,
    "Leigh_syndrome|Leber_optic_atrophy": 2,
    "Autosomal_recessive_early-onset_Parkinson_disease_6|Leigh_syndrome": 1,
    "MELAS_syndrome|Mitochondrial_disease|Leigh_syndrome": 1,
    "Leber_optic_atrophy|Leber_optic_atrophy_and_dystonia|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency|Mitochondrial_disease|not_provided|MELAS_syndrome|Leigh_syndrome": 1,
    "Abnormal_brain_morphology|Cognitive_impairment|Vertigo|Muscle_spasm|Paresthesia|Constriction_of_peripheral_visual_field|Headache": 1,
    "Leigh_syndrome|Retinal_dystrophy|Optic_atrophy|Mitochondrial_disease|not_provided|Leber_optic_atrophy": 1,
    "Striatal_necrosis|_bilateral|_with_dystonia|Leber_optic_atrophy|MELAS_syndrome|Mitochondrial_disease|Leigh_syndrome|Leigh_syndrome_due_to_mitochondrial_complex_I_deficiency": 1,
    "Leber_optic_atrophy|Leigh_syndrome|Auditory_neuropathy_spectrum_disorder": 1,
    "Mitochondrial_cytopathy": 2,
    "Leber_optic_atrophy_and_dystonia|Leber_optic_atrophy|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Leigh_syndrome|not_specified|Dystonic_disorder|Dysarthria": 1,
    "Leigh_syndrome|Parkinsonian_disorder|Blindness|Mitochondrial_disease": 1,
    "Mitochondrial_DNA-related_disorder": 2,
    "Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|MELAS_syndrome|Mitochondrial_disease|not_provided": 1,
    "Mitochondrial_disease|Diabetes-deafness_syndrome_maternally_transmitted": 1,
    "Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|not_provided|See_cases": 1,
    "not_provided|Mild_liver_congestion|Episodic_vomiting|Sudden_death|Developmental_delay|MELAS_syndrome": 1,
    "Inborn_mitochondrial_myopathy|Myopathy|_mitochondrial|_with_diabetes_mellitus|Diabetes-deafness_syndrome_maternally_transmitted|Mitochondrial_disease|MELAS_syndrome": 1,
    "Mitochondrial_disease|Cerebellar_ataxia|Gonadal_dysgenesis|Abnormal_basal_ganglia_MRI_signal_intensity|Progressive_spastic_paraparesis": 1,
    "Ovarian_neoplasm|not_specified": 6,
    "Familial_cancer_of_breast|not_specified|Leigh_syndrome|Venous_thromboembolism": 1,
    "Mitochondrial_disease|Parkinsonism/MELAS_overlap_syndrome": 1,
    "MT-CYB_associated_Exercise_intolerance|MT-CYB_associated_Mitochondrial_myopathy|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|Exercise_intolerance|Mitochondrial_disease": 1,
    "Leigh_syndrome|Mitochondrial_disease|Exercise_intolerance|_cardiomyopathy|_and_septooptic_dysplasia": 1,
    "not_specified|Familial_cancer_of_breast|Venous_thromboembolism": 1,
    "Leigh_syndrome|Epilepsy|Bilateral_lesions_of_basal_ganglia": 1,
    "not_specified|Ovarian_neoplasm": 4,
    "Ovarian_neoplasm|Leigh_syndrome": 4,
    "Sensorineural_hearing_loss_disorder|Reduced_visual_acuity|Ataxia|Atrophy_of_the_brain_and_cerebellum|Parkinsonism-plus": 1,
    "Leber_optic_atrophy|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|Exercise_intolerance|Mitochondrial_disease": 1,
    "Mitochondrial_encephalomyopathy|Leigh_syndrome|Mitochondrial_disease": 1,
    "Hearing_impairment|Macrocephaly|Developmental_delay|Leigh_syndrome": 1,
    "Familial_cancer_of_breast|Leigh_syndrome": 3,
    "Leigh_syndrome|Ovarian_neoplasm": 2,
    "not_specified|Leigh_syndrome|Mitochondrial_disease|Familial_cancer_of_breast": 1,
    "Leigh_syndrome|Leber_optic_atrophy|MELAS_syndrome|not_provided": 1,
    "Focal_white_matter_lesions|Ischemic_stroke": 1,
    "not_specified|Leigh_syndrome|Ovarian_neoplasm": 1,
    "Kearns-Sayre_syndrome|Progressive_external_ophthalmoplegia|MERRF_syndrome|MELAS_syndrome|Leigh_syndrome|Leber_optic_atrophy|NARP_syndrome": 1,
    "not_provided|Leigh_syndrome|Obesity": 1,
    "Leigh_syndrome|Histiocytoid_cardiomyopathy": 1,
    "not_specified|Familial_colorectal_cancer": 1,
    "Leber_optic_atrophy|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency|Multisystem_disorder|Mitochondrial_disease": 1,
    "Exercise_intolerance|Mitochondrial_myopathy_with_reversible_cytochrome_C_oxidase_deficiency": 1,
    "Leigh_syndrome|Familial_cancer_of_breast": 1,
    "not_provided|Leigh_syndrome|Mitochondrial_disease": 1,
    "Generalized_hypotonia|Neonatal_onset|Sudden_cardiac_death|Infantile_onset|Jaundice|Constipation|Failure_to_thrive|Variant_of_unknown_significance|Mitochondrial_disease": 1,
    "Familial_cancer_of_breast|MELAS_syndrome": 1,
    "not_specified|MELAS_syndrome|Ovarian_neoplasm": 1,
    "Ovarian_neoplasm|MELAS_syndrome": 1,
    "Parkinson_disease|_mitochondrial|MELAS_syndrome": 2,
    "MERFF_syndrome|MELAS_syndrome|Mitochondrial_disease": 1,
    "Mitochondrial_disease|Myopathy": 1,
    "MELAS_syndrome|MERRF_syndrome": 1,
    "MERRF_syndrome|Mitochondrial_inheritance": 3
  }
}